Moult and Ageing of European Passerines
First published 1994 by Academic Press Limited This edition published 2011 by Christopher Helm Publishers, an imprint of Bloomsbury Publishing Pic, 36 Soho Square, London W1D 3QY Copyright © 1994 Academic Press Limited The right of Lukas Jenni and FLaffael Winkler to be identified as the authors of this work has been asserted by them in accordance with the Copyright, Designs and Patents Act 1988. ISBN (print) 978-1-4081-5554-7 ISBN (e-pdf) 978-1-4081-5555-4 A CIP catalogue record for this book is available from the British Library All rights reserved. No part of this publication may be reproduced or used in any form or by any means — photographic, electronic or mechanical, including photocopying, recording, taping or information storage or retrieval systems — without permission of the publishers. This bo ok is produced using paper that is made from wood grown in managed sustainable forests. It is natural, renewable and recyclable.The logging and manufacturing processes conform to the environmental regulations of the country of origin. Printed in Great Britain by Martins the Printers, Berwick upon Tweed 10 9 8 7 6 5 4 3 2 1
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Moult and Ageing of European Passerines Lukas Jenni Schweizerische Vogelwarte Sempach Swiss Ornithological Institute
Raffael Winkler Naturhistorisches Museum, Basel Natural History Museum, Basel
Photographs by
Thomas Degen with additional material by Paul Mosimann, Christian Berger and the authors
CHRISTOPHER HELM LONDON
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Contents Preface
ix
PARTI Chapter 1 The function and consequences of moult
Chapter 2
.,1 1.2
Functions of the plumage Plumage maintenance and the need for plumage renewal 1.2.1 Feather maintenance and wear 1.2.2 Adjustments to the plumage 1.3 The costs of moult 1.3-1 Plumage efficiency during moult 1.3.2 Energetic, nutritional and metabolic demands of moult 1.4 Fitting moult into the annual cycle
1 2 2 2 4 4 4 5
The terminology of feathers, plumages, moults and age classes
7
2.1
7 7 8 8 8 9 9 9 9
2.2
2.3
Chapter 3
1
Arrangement of the feathers 2.1.1 Flight feathers 2.1.2 Wing-coverts Plumages, feather generations and moults 2.2.1 Concepts of moult and plumage terminologies 2.2.2 General terms 2.2.3 Moult terms 2.2.4 Terms for plumages, feathers and feather generations Age classes
The moult of adults
11
3.1 3.2
11 12 12 12 12 12 14 14 15 16 16 17 17 17 17 17 17 18 18 18 20 20 20 20 21 22
3.3
Introduction to the moult strategies Sequence of moult 3.2.1 Basic sequence of the complete moult Flight feathers Body-feathers and wing-coverts 3.2.2 Functional aspects of the basic sequence of moult 3.2.3 Variations and exceptions to the basic moult sequence Primaries Secondaries Tertials Rectrices Wing-coverts Variation in the relationships between flight feather tracts Moult strategies 3.3.1 Complete postbreeding moult in the breeding area: Moult strategies 1 and 2 Complete postbreeding moult in the breeding area Partial prebreeding moult 3.3.2 Complete moult in the non-breeding area: Moult strategy 3 Partial moult before autumn migration Suspension of the complete moult within the non-breeding area Additional prebreeding moult Conclusions 3.33 Seasonally divided moult of remiges: Moult strategy 4 Seasonally divided primary moult Seasonally divided secondary moult 3.3.4 Partial and complete biannual moult of remiges: Moult strategies 5 and 6
vi
Contents
3.4
Chapter 4
3.3.5 Conclusions Timing and duration of the complete moult 3.4.1 Timing and duration of the complete postbreeding moult in the breeding area Reduction of moult duration Overlap between breeding and moult Overlap between moult and autumnal activities Arrested moult Moult duration Timing of moult 3.4.2 Timing of moult in trans-saharan migrants
22 23 23 23 24 24 25 25 25 26
The moult during the first year of life
29
4.1 4.2
29 29 29 29 31 31 31 31 32 32 32 32 32 32 34 37 37 38 38 39 40 40 41 41
4.3
4.4
4.5 4.6
Introduction to the moult cycles The juvenile plumage 4.2.1 Completion of the juvenile plumage after fledging 4.2.2 Structure of the juvenile plumage 4.2.3 Coloration of the juvenile plumage Sequence of postjuvenile moult Complete postjuvenile moult Partial postjuvenile moult 4.3.1 Sequence within wing-feather tracts during partial postjuvenile moult Wing-coverts and alula Tertials Secondaries Rectrices 4.3.2 Relationship between wing-feather tract renewal during partial postjuvenile moult 4.3.3 Sequence of eccentric and other partial primary moults Partial postjuvenile moult in the breeding area 4.4.1 Variation in extent, timing and duration: experimental evidence of control of postjuvenile moult 4.4.2 Interspecific variation in timing and extent Timing and duration Extent 4.4.3 Intraspecific variation in timing and extent Variation with hatching date Differences between populations Differences between the sexes and effects of energetic and nutrient stress Intraspecific variation in the extent of postjuvenile moult during the course of the non- breeding season and between wintering sites 4.4.4 Partial postjuvenile primary moult in the breeding area Complete postjuvenile moult in the breeding area Moults during the first year of life in trans-saharan migrants 4.6.1 Partial postjuvenile and partial prebreeding moult excluding remiges: Moult cycles 5 and 6 4.6.2 Complete moult in the non-breeding area: Moult cycles 9, 10, 11, 14 and 15 4.6.3 Partial moult including remiges in the non-breeding area: Moult cycles 7, 8, 12 and 13 First partial prebreeding moult including secondaries First partial prebreeding moult including primaries Incomplete first prebreeding moult 4.6.4 Conclusions
41 43 44 45 45 45 46 46 46 46 47
PART II Chapter 5
Ageing European passerines
49
5.1 5.2
49 49 49 50 50 50 50 51 51
Ageing criteria in live birds Ageing using plumage characters 5.2.1 Recognition of juvenile feathers Structure and shape Coloration Wear Growth bars and fault bars 5.2.2 Differences in extent of moult 5.2.3 Differences between postjuvenile and subsequent feather generations
Contents 5.3
Chapter 6
General ageing criteria in European passerines based on moult 5.3.1 Species with a complete postjuvenile moult in the first summer/autumn: Moult cycle type 1 5-3.2 Species with a partial postjuvenile/complete postbreeding moult in the breeding area: Moult cycle type 2 5-3.3 Species with a partial postjuvenile/complete postbreeding moult in the breeding area and a partial prebreeding moult in winter/spring: Moult cycle type 3 5.3.4 Species with a complete moult in the non-breeding area
vii 52 52 52 54 57
Species accounts
61
Presentation of the data and directions for use Material Relevance of the data Presentation and analysis of the data Procedure of ageing Species accounts Riparia riparia, Sand Martin Hirundo rustics Swallow Delicbon urbica, House Martin Anthus campestris, Tawny Pipit Anthus trivialis, Tree Pipit Anthus pratensis, Meadow Pipit Anthus spinoletta spinoletta, Water Pipit Motacilla flava, Yellow Wagtail Motadlla cinerea, Grey Wagtail Motacilla alba alba, White Wagtail Troglodytes troglodytes. Wren Prunella modularis, Dunnock Erithacus rubecula, Robin Luscinia megarhynchos, Nightingale Luscinia svecica, Bluethroat Phoenicurus ochruros, Black Redstart Phoenicurusphoenicurus, Redstart Saxicola rubetra, Whinchat Oenanthe oenanthe, Wheatear Turdus torquatus. Ring Ouzel Turdus merula, Blackbird Turduspilaris, Fieldfare Turdusphilomelos, Song Thrush Turdus iliacus, Redwing Turdus viscivorus, Mistle Thrush Acrocephalus scirpaceus, Reed Warbler Hippolais icterina, Icterine Warbler Sylvia curruca, Lesser Whitethroat Sylvia communis communis, Whitethroat Sylvia borin, Garden Warbler Sylvia atricapilla. Blackcap Phylloscopus collybita, Chiffchaff Phylloscopus trochilus, Willow Warbler Muscicapa striata, Spotted Flycatcher Ficedula hypoleuca^ Pied Flycatcher Parus ater, Coal Tit Parus caeruleus, Blue Tit Parus major, Great Tit Sitta europaea, Nuthatch Oriolus orioluSj Golden Oriole Lanius collurio, Red-backed Shrike • Garrulus glandarius, Jay Fringilla coelebs. Chaffinch Fringilla montifringilla, Brambling Serinus serinus, Serin Serinus citrinella, Citril Finch Carduelis chloris, Greenfinch Carduelis carduelis, Goldfinch
61 61 61 61 62 63 64 65 66 68 71 73 76 80 83 87 89 91 94 95 96 99 101 104 107 109 111 113 115 116 118 119 121 123 127 130 133 136 138 141 146 148 150 152 153 154 156 158 161 163 166 168 171
viii
Contents
Carduelis spiniiS) Siskin Carduelis cannabina^ Linnet Carduelisflammea cabaret, Redpoll Loxia curvirostra> Crossbill Pyrrhulapyrrhula, Bullfinch Coccothraustes coccotkraustes, Hawfinch Emberiza citrinella^ Yellowhammer Emberiza ciay Rock Bunting Emberiza hortulana. Ortolan Bunting Emberiza schoenidus, Reed Bunting
APPENDIX
The use of skull pneumatization for ageing The process of skull pneumatization Recognition of skull pneumatization Skull pneumatization scores Age determination by skull pneumatization Explanations of the graphs
173 177 180 182 188 189 191 193 195 198
201 201 201 203 203 203
References
209
Scientific names with their English, German, French, Italian and Spanish translations
219
Species Index
222
Explanations
224
Preface This book has two complementary aims. First, it presents an up to date summary of the moult patterns of European passerines with due emphasis on the extent of partial moults. This information is then used to demonstrate, with the aid of photographs, detailed ageing criteria for 58 species. Although not an exhaustive reference work on all aspects of moult and ageing in European passerines, the book is thought to be a valuable complement to other guides, both through its extensive photographic references and detailed discussion of the extent, sequence and strategies of moult. Part I gives an overview of the various moult patterns and strategies of European passerines based on our own observations and on data from the literature. Until now, most moult studies have investigated the timing, duration and sequence of moult by concentrating on actively moulting birds, and these aspects thus dominate the moult literature (summarized in e.g. Bub 1981, 1984, 1985, Bub & Herroelen 1981, Kasparek 1981, Ginn & Melville 1983, Glutz & Bauer 1985, 1988, 1991, Bub & Dorsch 1988, Cramp 1988, 1992, Rymkevich 1990, Svensson 1992, Cramp & Perrins 1993). For most species, the process of moult and how it is fitted into the annual cycle is well described, although the emphasis tends to be on the complete moult of the adults. In order to further our understanding, we particularly investigated the extent of partial moults, which have been much less thoroughly studied. Few species have been examined in detail in this respect and the information is often not readily available to the non-specialist. Recently, a detailed synopsis on the timing and duration of moult of passerines in NW Russia, including data on the extent of moult, was published by Rymkevich (1990). Since the extent of a partial moult can only be recognized after the moult is completed, we do not focus on the process of moult, but on the result of this process. This requires the recognition of the different feather generations of birds which have completed their moult, a technique widely used for ageing. Partial moults are of particular interest because they vary between and within species not only in timing and duration, but particularly in extent, a parameter clearly visible until the next moult. In contrast to timing and intensity, the extent of moult has direct effects beyond the actual moult period, such as on the quality of the plumage and its appearance. Thus, timing, duration, sequence and extent of moult are all important features in studies of the ecological functions of moult. We hope that the detailed description of partial moults given in this book will stimulate further studies in this area of investigation. Various moult strategies and extents of moult result from the amount of time available for moult and on how moult is fitted into the annual cycle. Until now, moult strategies have usually been described only by reference to the moult of the remiges. We have tried to describe the moult strategies of European passerines based on the seasonal occurrence and extent of moults of the entire plumage, which may provide a more realistic insight into the inter- and intraspecific variations in how moult fits into the annual cycle. Our account also highlights how incomplete is our knowledge of the moult strategies of trans-saharan migrants. The sequence of moult was generally thought to be relatively uniform among passerines and to show special adaptations in a few species only. However, as shown in chapters 3 and 4, a variety of moult sequences actually occur, In this book, we provide an up to date account of these less well known moult sequences, supplemented by our own observations.
Part II provides a general introduction to ageing by plumage characters followed by the species accounts. A knowledge of the moult cycle of a species and the variation in extent of its moult, is a prerequisite for ageing using plumage characters. We have therefore tried to explicitly deduce ageing criteria from the observed moult patterns. This results in the recognition of four main moult cycle types among the passerines breeding in Europe and a description of their corresponding general ageing criteria (chapter 5). We hope that this procedure, together with the information given in the first part of the book, will enable one to more easily age birds in active moult, to appreciate unusual and undescribed moult patterns and their implications for ageing and to develop plumage ageing criteria for species not previously studied in detail. The species accounts provide detailed information on the range of extent of moult for 58 species and explain how this information can be used for ageing. Thus, we avoid giving mere rules based on the most frequent moult patterns. We are well aware that the data given on the extent of moult relate mainly to central Europe and that the restricted number of species treated prohibits the use of this book as a general ageing guide to European passerines (cf. Svensson 1992). However, the main aim is to convey, with the examples given and with the general ageing criteria provided in chapter 5, how feather generations can be recognized and how plumage ageing criteria can be deduced. The colour photographs illustrate the variation in moult patterns and the recognition of feather generations and, hence, ageing criteria. They replace tedious descriptions of feather wear and colour differences and should also speed up the process of acquiring a feel for the clues to ageing a particular species. However, many ageing criteria rely on the recognition of very slight differences in colour and wear, and some experience in recognizing them is certainly required. In the colour photographs, we concentrated on the wing since most plumage ageing criteria are to be found there. Almost the whole range of moult extent is reflected since the marginal coverts are among the first, and the secondaries among the last tracts to be moulted. There are a number of ageing criteria other than plumage characters, e.g. iris colour, colour of the inside of the upper mandible and skull pneumatization. In the section 'best criteria' we mention such other useful ageing criteria, especially if they are more reliable and more easily recognized than plumage characters. However, with the exception of skull pneumatization, we cannot treat them in detail, because we only rarely tested their reliability quantitatively. This is the aim of an ongoing project by Swedish colleagues (Karlsson etal. 1985). Within the section 'best criteria', we systematically provide the period of validity of skull pneumatization for ageing based on our own data presented in the Appendix. In contrast to North American practice, skull pneumatization is not very widely used for ageing birds in the Old World, although it is a very reliable criterion for many species in summer and autumn, when it offers the possibility to check the reliability of newly discovered or ambiguous ageing characters. Many of the ageing criteria and unusual moult patterns described here could only be verified by skulling. Also, certain ageing criteria mentioned in the literature could be shown to be unreliable. The moult data and the colour photographs presented here were collected at several bird ringing stations in Switzerland in autumn and spring, on Ventotene Island, Italy in spring and from the collection of the Natural History Museum, Basel (details see chapter 6). Our interest in moult arose in 1972, but systematic data collection started in 1980.
x
Preface
In total, moult data have been taken from about 140,000 birds by the authors and by Paul Mosimann, Christian Berger, Markus Leuenberger and Thomas Degen. Skull pneumatization was recorded for all birds observed in the summer/autumn. All the photographs were taken from live birds, except about 20 which were from wing preparations in the Natural History Museum, Basel. A special method for taking photographs of wings was developed by Thomas Degen. The feathers of the right wing were carefully arranged with a pair of fine tweezers. Then, the wing was placed on an oblique board covered with a standard grey paper. A small piece of double-sided adhesive tape, 1.5 mm thick, held the wing just distally of the wrist. Photographs were taken on 35 mm slide film, 64 ISO, with a reflex camera mounted on a tripod and equipped with a ring flash. This relatively simple technical equipment had the advantage that it was easy to transport and to install, even in the field. A disadvantage was the inability to ensure exact equivalence of the colours between the slides. For our purpose, however, absolute colours are not so important as relative differences in colour between feathers on the same wing. This work would have been impossible without the tremendous help of many people and we are greatly indebted to them all: Christian Berger, Thomas Degen, Markus Leuenberger and Paul Mosimann showed great enthusiasm and perseverence in the collection of moult
data and photographs during several years. Others too numerous to name assisted at the bird ringing stations in Switzerland although Hildegard Messerknecht and Roland Ammann deserve our special thanks. Ernst Sutter laid the foundations of the carefully documented skin collection in the Natural History Museum, Basel, and provided the data for Garrulus glandarius. Fernando Spina, head of the Italian Ringing Scheme, enabled Raffael Winkler and Paul Mosimann to work on Ventotene Island. Peter Keusch, John Attard Montalto and Frank Neuschulz made it possible to catch and take photographs of Emberiza hortulana, Cisticola juncidis and Sylvia nisoria in their study areas. Markus Leuenberger and Thomas Degen helped with the analysis of the data. Les Underbill carried out the analyses of the dependence of moult extent on skull pneumatization scores and feather-length. Unpublished data were provided by B. Bruderer, C. de la Cruz, A.A. Dhondt, T. Fransson, C, Gauci, H. Leuzinger, A. Lindstrom, G. Nikolaus, D.J. Pearson, W. Priinte, F. Spina, J. Sultana and M. Widmer. T. Wesofowski translated important literature from Russian. E. Gwinner, D.G. Homberger, A. Lindstrom and D.J. Pearson provided valuable comments on earlier drafts of parts of the manuscript. Andrew Richford, editor and ornithologist at Academic Press, was a constant source of advice and encouragement.
PARTI CHAPTER 1
The Function and Consequences of Moult 1.1 Functions of the plumage The process of moult serves to keep the plumage in good condition and adjust its characteristics to the changing needs of a bird during its lifetime. Therefore, understanding moult requires a knowledge of the various functions of the plumage, Feathers form a flexible and light-weight protective barrier against mechanical impact, solar radiation and water. In addition, the plumage is the main layer of thermal insulation and plays an important role in thermoregulation. Short-term adjustments to the degree of insulation can be effected by changes in the position of the feathers. Long-term adjustments can be made by changing the number, mass or length of the feathers, by feather loss or by growing additional or differently structured feathers during moult (see section 1.2.2). The unique function of feathers is that they enable birds to fly by forming the major part of the airfoil-like wings and by clothing the body in an aerodynamically favourable shape. The plumage is also largely responsible for the appearance of the bird, giving it its colour and shape and thus is important for visual communication and camouflage. Specially coloured parts or adornments have often evolved which may be apparent only in one sex or only during a certain time of the year. Many other functions of the plumage or feathers only appear in certain taxa or species (mainly non-passerines), e.g. regulation of buoyancy (in waterfowl), production of sound (e.g. in snipe), deadening of sound produced by the wings (in owls and nightjars), transport of water (in sandgrouse), aid in hearing (in owls), mechanical support (in woodpeckers and treecreepers), tactile sensitivity (e.g. in kiwis), provision of nesting material (in certain waterfowl) and help in digestion (in grebes). Some functions of the plumage are in potential conflict with each other. Thus, the best plumage is a well-balanced compromise between opposing requirements which may differ between species, sexes, age classes and seasons. For instance, flight feathers are under strong selection pressure for optimum flight performance, and this generally impedes the evolution of elaborate adornments. There is a general conflict between the need for crypsis and conspicuous signal coloration. Compromise solutions to this conflict include: distinctive colour patterns which are unusual or easily distinguished close to, but are cryptic at long range, as opposed to conspicuous coloration which is easy to see at a distance (Butcher & Rohwer 1989); reduction of conspicuous coloration to certain feathers which are normally hidden and are presented only on certain occasions; changing the colour of the plumage seasonally through the abrasion of cryptic feather fringes or by moulting twice a year; confining conspicuous coloration to one sex or to certain age groups only. The compromise between conspicuousness and crypsis or between adornments and flight capability has been interpreted as a way in which $ can honestly advertise their own quality to potential mates or rivals by displaying a genuine handicap which they clearly have overcome (e.g. long tail-feathers which reduce flight capacity or foraging efficiency; coloration which is conspicuous to predators; Zahavi 1975, 1977). A further conflict may arise since feathers exposed to intense wear should not be light in colour (Burtt 1986), because a high melanin content (which gives black, brown, redbrown and yellow colours) increases their durability (Fig. 1 and 2). This may conflict with the colour requirements of camouflage or
display. On the other hand, plumage coloration and heat gain from solar radiation are more or less independent, because colour is only one of several factors determining the penetration of radiation into the plumage (Walsberg 1983). Very few studies have tried to use an integrated approach to understand how the various requirements determine the properties of the plumage. In a pioneering study, Burtt (1986) examined how feather durability, energy balance, communication behaviour and camouflage requirements interacted to determine the plumage colour of New World Parulidae. Our incomplete knowledge of the significance of plumage properties makes it difficult to always understand the timing, extent and sequence of moult of a particular species or individual.
Fig. 1. Carduelis carduelis ad $, 22 October. The whole plumage is fresh, the tertials, secondaries and primaries having unworn, white tips.
Fig. 2. Carduelis carduelis ad 6*, 25 April. The plumage is worn. Note how abrasion has especially affected the less resistant white tips of the exposed tertials and outer primaries. However, the white tips remain on the protected inner primaries and secondaries.
2
The Function and Consequences of Moult
1.2 Plumage maintenance and the need for plumage renewal Full-grown feathers are dead structures consisting mainly of avian keratin. Keratin is one of the most durable biological materials, with great strength, flexibility and resistence to hydrolytic, protein-digesting enzymes and bacteria. However, unlike other keratin structures like hair and claws, they cannot be renewed continuously from the base. Consequently, unsuitable feathers must be replaced totally. Furthermore, feathers can only be replaced by pushing out the old feather long before the new one is fully grown and functional. This is a major disadvantage of feathers since it results in a significant reduction in plumage function when many feathers must be replaced simultaneously. The regular replacement of all or part of the plumage is called moult. There are two main reasons for plumage renewal. (1) Damaged or lost feathers need to be replaced in order to maintain the function of the plumage. (2) A plumage unsuitable for ensuing purposes must be replaced in order to adjusts to the new requirements.
also on the behaviour of the bird (see Fig. 4—6). Generally, the more loosely textured feathers of the juvenile plumage are more prone to abrasion than the feathers of subsequent generations (Fig. 7). Exposed feathers abrade and bleach more readily than concealed feathers (Fig. 4-7). In many species, the tertials, rectrices, inner, but not the innermost tenth, greater coverts and the tips of the outer primaries are especially exposed, The secondaries, inner primaries and primary coverts, outer greater coverts and the carpal covert are normally well protected (Fig. 4—7). This difference in exposure may lead to situations in which feathers generated more than six months apart can no longer be distinguished by the degree of wear (see p, 66, 76, 124). Durability also depends on pigmentation. Feathers, or parts of feathers, carrying melanin pigments are more durable than those without melanin (Burtt 1986, Fig. land 2). The fact that the extent of wear differs with habitat, climate, weather and exposure of the feather always has to be kept in mind when assigning feathers to different feather generations and in reconstructing the extent of moult in birds outside the moulting season.
1.2.1 Feather maintenance and wear
1.2.2 Adjustments to the plumage
Feathers are regularly maintained by a variety of comfort behaviours such as preening, scratching, shaking, bathing and drying, oiling with the secretion from the preen gland, dusting, sunning and possibly anting (Simmons in Campbell & Lack 1985). Inevitably, however, feathers are lost or irreparably damaged through mechanical abrasion, photochemical processes, ectoparasites, bacteria and fungi. If not pathological, we subsume all these factors under the more general term 'wear' (other authors use the term 'abrasion* in the same general sense; e.g. Ginn & Melville 1983, Rogers 1990). Whole feathers may be lost through traumatic mechanical interaction with vegetation, the nest, conspecifics or predators. Feathers may also be lost under the stress of'fright moult' (Dathe 1955, Stiefel in Bub 1985, Lindstrom & Nilsson 1988) and in forming the brood patch (Schifferli 1981). Abrasion, caused by rubbing against other feathers, objects in the environment and particles in the air, damages the structure of the feathers by breaking off the barbicles and barbules and by cracking and splitting the barbs and the rachis (Burtt 1986). This impairs or may completely prevent the cohesion of the vane. Abrasion of the exposed and often looser textured feather fringes diminishes the surface area and may substantially change the shape of the feather (Fig. 5). Abrasion also affects the colours of the plumage. The feathers of many birds have dark centres and light fringes. Through wear, the plumage increasingly takes on the colour of the feather centres and may become less cryptic. Feathers are damaged by sunlight: ultraviolet light alters the physical structure of keratin and pigments leading to bleaching. Ectoparasites such as lice (Mallophaga) and feather mites (Acari) actually eat feather material. Regular moult may help to reduce the load of ectoparasites, as suggested by the lower number of Mallophaga found in an American Emberizine bunting (Ammospiza caudacuta) which moults twice a year, compared with a similar species (Ammospiza maritimd) moulting only once a year (Post &Endersl970). Wear depends on habitat, weather, climate and season. Birds sliding through dense, hard vegetation such as reeds, grass, sedges or thorny bushes, or exposed to sand and wind suffer more abrasion than aerial and perching birds. Birds exposed to intense sunlight suffer more bleaching than those living in shady forests (cf. Fig. 3 with Fig. 4-6). Bleaching may be more pronounced in tropical winter quarters than in the temperate breeding area. Changes in wing-length indicate that abrasion may be stronger during the breeding season (due to activities in the nest and intensive foraging) than outside the breeding season (van Balen 1967, Flegg & Cox 1977, Francis & Wood 1989). Wear affects different feathers differently depending on the exposure, shape, structure and pigmentation of the feather in question and
Birds may need to adjust their plumage in response to seasonal changes, age and changing environmental conditions. For some time, studies have centered on the description of changes in plumage coloration according to age and season, but only recently has it been realized that the actual plumage structure may also change. Many passerine species have a distinct juvenile plumage (see section 4.2) which is usually replaced with a more colourful adult plumage within the first year. In some sexually dimorphic passerines, first-year cT acquire a more 9 -like plumage rather than the adult- cT plumage, although they may in fact breed. This delayed plumage maturation has been explained in various ways (see e.g. Lawton & Lawton 1986, Rohwer & Butcher 1988, Butcher & Rohwer 1989). In a few species, the adult plumage may also become slightly more colourful with increasing age (e.g. Ficedula hypoleuca, Winkel et aL 1970; Saxzcola rubetra> Schmidt & Hantge 1954). As mentioned earlier, the requirements of camouflage and display may be in conflict. In many species, their relative importance differs depending on season or on the age of the bird. Therefore, it may be advantageous for birds to change their appearance during the year, or as they age. Apart from temporary exposure of normally concealed colourful feather patches or conspicuous structures, there are two ways in which appearance may be altered. First, abrasion is a limited, but nevertheless striking method of changing plumage colour. Well known examples are the light fringes on the body-feathers of species such as Fringilla coelebs, F. montifringilla, Carduelis cannabina, Sturnus vulgaris etc., which are worn away during winter to disclose the colourful or shiny breeding plumage in spring. Abrasion of these fringes is often facilitated by their light colours, which contain little or no melanin. The second method of changing the appearance is by moulting. It is the only way to profoundly change appearance with age or seasonally and to introduce special feather structures. Species having more than one moult per year usually change between a colourful 'display' plumage worn during the mating season, and a more cryptic, dull 'eclipse' plumage worn during the rest of the year (see section 3.3.1). Many species change from a cryptic juvenile plumage to a more colourful adult plumage (see section 4.2.3). Less well studied are changes with age and with environmental conditions of plumage structures important in behaviour and display. Many plumage characters which play a role in sexual selection, aggressive encounters and establishing dominance in non-breeding flocks are less prominent in first-year birds than in older ones. It has been shown recently that the extent of an apparent handicap (the length of the tailfeathers in S of the African sunbird Nectariniajohnstoni) varies yearly with differing food availability and weather conditions (Evans 1991). It
Plumage maintenance and the need for plumage renewal
Fig, 3. Sylvia atricapilla ad 9 , 2 5 April. The whole plumage is postbr. This species shows hardly any signs of wear in spring, although the plumage was acquired about nine months previously.
3
Fig. 5. Calandrella brachydactyla, 23 April. The whole plumage is postbr or postjuv. The feathers, acquired about nine months previously, are considerably abraded. In this species living in a sunny, dusty environment and running though grassy vegetation, wear has primarily affected the tertials, the innermost greater coverts and the outer webs of the inner secondaries, which are most exposed when the wing is closed. The primaries and outer secondaries are protected by the long tertials, and the central and outer greater coverts and the primary coverts by the inner greater coverts, and are thus hardly worn.
Fig. 4. Sylvia canttllamiA <3, 21 April. The whole plumage is postbr, except for some MaC and MeC, GC 4 and possibly T which are prebr. The postbr feathers acquired about nine months before are noticeably abraded and bleached. In this species wintering in the tropics and flying through thorny scrub, wear has primarily affected the exposed tertials, the inner greater coverts (except the protected GC 10), the tips of the primaries and the outer primary coverts. The tips of the protected secondaries are hardly worn, while the more exposed fringes of their outer webs are slightly abraded.
Fig. 6. Saxicola torquata 2y 6, 1 May. The MaC, MeC, GC, CC, Al 1 > T and 56 are postjuv, the rest of wing juv. The feathers acquired 8-12 months previously are considerably worn. In this sit-and-wait predator, hunting prey mainly by flying into low vegetation, wear has mainly affected the tips of the remiges, including the secondaries, these feathers being those exposed when the wing is open. The relatively short tertials and the greater coverts are less worn, both because they are less exposed on the open wing and because they have been renewed in summer/autumn.
seems that conditions prevailing during moult or some clue to the likely future conditions perceived at the time of moult, determines the extent of the handicap a <5 can tolerate and show off to 9. Thus, moult provides a means to adjust an individual's status and quality signals to its age and to the environmental conditions at the time. The plumage performs other functions, apart from governing appearance, which may be adjusted according to season and age and which have been little studied. It is well known that the juvenile remiges are usually shorter than their successors, with the exception of the outermost primary which is usually longer. The shorter length of the juvenile remiges is usually ascribed to nutritional constraints during the nestling period. However, this more rounded and slotted wing of juveniles may be an adaptation to increase flight manoeverability during the first phase of independence (Alatalo etal. 1984). According to this hypothesis, moult of the remiges would be necessary to change the wing-shape of young birds to the adult shape as flight experience
increases. However, a convincing test of this hypothesis, taking into account differences in body mass between juveniles and adults, is still lacking. In species with two moults per year, the amount of insulation provided by the plumage could be adjusted to suit the seasons. This has been observed in Carduelis tristis. The number and length of prebreeding and postbreeding body-feathers is similar, but the postbreeding ones have more plumaceous barbules resulting in a considerably heavier 'winter' plumage (Middleton 1986). In birds with only one moult per year, changes in plumage insulation may be effected through feather loss and wear. It has been shown in some species that the number and/or mass of the body-feathers is higher just after the moult than before it (e.g. Wetmore 1936, Staebler 1941, Brooks 1968, Newton 1968b, Clench 1970, Schifferli 1981, Wijnandts 1984). Since body-feathers are lost throughout the year, it would be advantageous to restore the plumage and so increase insulation before the winter in cold
4
The Function and Consequences of Moult
Fig. 7. Serinus serinus 2y <3, 5 May. The MaC are postjuv, the MeC 1â&#x20AC;&#x201D;4+6+8 juv, and MeC 5+7 postjuv. The rest of the wing is juv. The loosely textured juvenile median coverts were acquired about ten months previously and are more worn than the more firmly textured postjuv median coverts acquired about nine months earlier. Within the feather tracts, wear has primarily affected the inner greater covens (except the protected GC 10) which lie over the outer ones and cover them when the wing is closed. Within the median coverts, however, the outer ones lie over the inner ones and are thus more heavily worn.
and temperate climates. Indeed, total insulation has been found to be better after moult than before it (e.g. Pohl 1971, Dolnik & Gavrilov 1979, King 1980). Likewise, feather loss at the approach of the warmer season may also be adaptive (Wetmore 1936). Additional evidence comes from Wetmore (1936), who noticed that some species had a lower number of feathers during the autumn, just after moult, than at the end of winter and concluded that body-feathers might be growing after the main moult period. The lighter, less dense and more loosely structured juvenile plumage might need replacement before wintering in cold areas. Thus, the postjuvenile moult probably increases the insulation effect for the oncoming winter. In a tropical dove (Streptopelia senegalensis), however, there seems to be no change in the number of feathers over the year (Markus 1963). The two main functions of moult, replacing worn feathers and adjusting plumage characteristics, will often be cited in chapters 3 and 4 in explanation of particular moult strategies or the extent of a partial moult. However, it is often impossible to distinguish between them, because our knowledge of the degree and effect of feather wear and the exact requirements of plumage function (especially the behavioural significance of particular plumage colours) is still poor.
1.3 The costs of moult The periodic replacement of the plumage entails two sorts of cost. (1) During moult, the functions of the plumage cannot be fully maintained. (2) The replacement of feathers requires energy and special nutrients as well as metabolic and physiological adaptations. These costs, obviously, depend on the number of feathers growing at any one time. The question is to what extent these costs compromise a bird's ability to maintain its normal lifestyle during moult.
1.3.1 Plumage efficiency during moult During moult, the number of fully formed feathers is reduced and this must affect plumage function. The most significant impacts are probably on flight performance, insulation, water repellency and the effectiveness of display. Thus, simultaneous moult of too many feathers would be especially disadvantageous during cold seasons, during periods in which efficient flight is important (e.g. on migration or when feeding young), during courtship and at times when territoriality
or social hierarchies operate. In general, the degree to which the plumage remains effective during moult depends in the first place on the speed of moult, i.e. predominantly on the rate at which feathers are shed and secondarily on the rate of new feather growth. The sequence of moult, which is especially strict for the flight feathers, appears to provide a means for minimizing the adverse effects of moult (see section 3.2.2). There are, however, surprisingly few studies on the effect of moult on plumage function. It has long been known that moulting birds adopt inconspicuous behaviour and refrain from singing. Birds moulting several remiges simultaneously become even more skulking and reluctant to fly, especially in the open (Newton 1966, Dolnik & BIyumental 1967, Haukioja & Kalinainen 1968, Haukioja 1971, Ginn 1975). In small passerines, simultaneous moult of more than about five primaries results in serious flight impairment or almost complete Sightlessness. In these species, alterations in the normal sequence of flight feather moult (see sections 3.2.2 and 3.2.3) help to guarantee a minimal flight capability. One would expect plumage insulation to suffer during the moult of body-feathers, especially when a large proportion of body-feathers is growing simultaneously, and increased thermoregulatory costs have indeed been found in moulting birds (e.g. Lustick 1970, Dolnik & Gavrilov 1979, Wijnandts 1984, Dietz et al 1992). However, it remains to be shown what proportion of these additional costs is due to the loss of insulating feathers, compared to the heat loss from the increased peripheral blood flow and increased evaporation involved in new feather growth (King 1980).
1.3.2 Energetic, nutritional and metabolic demands of moult Moult entails significant additional energy costs, since about 5â&#x20AC;&#x201D;10% of total body mass or 20-30% of the total lean dry body mass of a passerine is replaced during a complete moult. These energetic costs include: the calorific content of the new feathers and the feather sheath; the energy required in their synthesis; and the energy required to produce and maintain the tissues involved in feather production (e.g. feather pulps). There are also a number of gross physiological modifications associated with moult, e.g. changes in body composition, increases in total blood volume, body temperature and body water turnover; altered bone metabolism; energy spent storing and supplying essential amino acids at night and the associated increase in body protein metabolism; extra energy lost from decreased plumage insulation and increased peripheral blood flow in the growing feathers (Murphy et al. 1990, Murphy & King 1991, 1992, Dietz et al. 1992). These metabolic processes and the increase in heat loss through poor insulation may explain the extremely low energetic efficiency of feather synthesis (2.6-6% in small passerines and 20% in Falco tinnunculus\ Dolnik & Gavrilov 1979, Murphy & King 1991, Dietz et al. 1992, Lindstrom etal. 1993). One estimate of the extra daily energy costs for a small passerine undergoing a reasonably rapid complete moult, lasting 54 days, is between 3% (early and late on in moult) and 20% (at the peak of moult) of the daily energy expenditure of non-moulting birds (Murphy & King 1992). However, Lusdnia svecica and Carduelis flammea showed that basal metabolic rates doubled at peak moult, a substantial extra demand on the daily energy budget (Lindstrom et al. 1993). However, it is still uncertain to what extent the additional energetic and physiological costs of even a rapid complete moult entail a period of stringency (Murphy & King 1992). In cases of slow or partial moult especially, the extra energetic and metabolic demands of moult may not be a sufficient explanation for the observed temporal separation of moult and other activities in a bird's annual cycle. During a rapid
Fitting moult into the annual cycle
moult, the increase in energy expenditure due to moult may be at least partly offset by a reduction in other activities such as locomotion or singing (King 1980, Lindstrom etai 1993). A generally restful lifestyle at this time may also serve to protect the growing and fragile feathers from undue wear and tear. So far, no studies have examined to what extent moult may be not only incompatible with other behaviours (such as reproduction and migration) because of the energetic costs, but also because of physiological conflicts, especially amino acid metabolism. For instance, it is difficult to imagine how the amino acid metabolism involved in an intense moult may be compatible with the special requirements of egg formation or fasting during long-distance flights (cf. Jenni-Eiermann & Jenni 1991). This problem may be more acute for small birds, with their high mass specific energy rate, than for larger birds. The discussion so far suggests several ecological considerations which may help to explain the variety of moult strategies. Feather synthesis at night requires complex and costly modifications to the metabolism of amino acids, compared with daytime synthesis, so the overall costs of moult may be lower in areas with relatively longer daylength (Murphy & King 1991, but see Lindstrom et at. 1993), Thus, birds moulting in late summer at high latitudes could shorten the duration of moult without increasing their daily energy costs, compared with conspecifics moulting in more southern areas. Dietz et al. (1992) estimate that the costs of increased heat loss during moult are probably more important than the energy required for feather synthesis. Therefore, ambient temperature may be an important factor determining the optimum timing of moult. Also, selection of a diet adequate in specific nutrients would help to reduce the energetic costs of moult (cf. Dietz et al. 1992). Indeed, selective feeding on foods rich in protein or sulphur amino acids has been shown experimentally (Murphy & King 1991) and may be the reason for changes in food choice observed in the field during the moulting period. Ultimately, the availability of certain foods may be another factor influencing the place and timing of moult. In summary, the importance of the various costs of moult, reduced efficiency of the plumage and increased energy requirements and the extra nutritional and metabolic demands, are still not well known. The direct energetic costs of moult alone may not be as important in determining the timing of moult as the literature might suggest. Indirect costs, such as the consequences of reduced plumage efficiency, especially in flight, and the radical alterations in physiology associated with moult, might be as relevant in explaining the temporal separation of moult, breeding and migration (cf. Earnst 1992).
1 A Fitting moult into the annual cycle It is clear so far that the selective forces influencing moult regime are on the one hand related to the declining quality of the feathers and the changes in plumage function, and on the other hand to the reduction of plumage efficiency and the energetic, metabolic and physiological requirements during moult. The bird must, in effect, make a difficult choice: when is the most appropriate time to moult?; which feathers should be replaced, at which rate and in which sequence?; to what extent must plumage performance be maintained during moult? It must also be able to adapt the timing and speed of moult to its own particular annual cycle and to changing environmental conditions. This intimate interaction between moult and the life of a bird is particularly critical during three other demanding periods, namely during breeding, migration and when under food stress, especially in winter or in cold weather conditions. A bird's particular moult strategy is the outcome. The moult strategies adopted by European passerines are actually rather uniform, compared with the diversity shown among birds in general. All European passerines usually renew the entire plumage at
5
least once a year. Whether this is always due to the actual need to replace worn feathers is uncertain. In some species, it may be a consequence of the particular annual cycle in the seasonal environment in which it originally evolved. European passerines moult during distinct, annually recurring periods. Most renew the entire plumage during a single, relatively short period while only a few divide complete plumage renewal between two moult periods. Other moult periods may be added, usually so that part of the plumage may be renewed more often than once a year. This is in contrast to large birds and certain tropical passerines which may moult more slowly over longer periods, sometimes lasting for much of the year, and in which a temporal division of a single moult cycle is more frequent (e.g. Stresemann & Stresemann 1966, Bloesch et al. 1977, Sutter 1980, Edelstam 1984, Zann 1985). Two factors may account for the regular, distinct and restricted moult periods typical of European passerines. First, due to their small size, small birds can moult completely relatively quickly while maintaining a high degree of flight capability. Large birds, however, need longer to perform a complete moult if they maintain a similar degree of flight capability (Stresemann & Stresemann 1966), or become flightless when moulting quickly (e.g. swans, geese, ducks). For example, vultures depend on their soaring ability to find food and so complete a slow continuous moult cycle lasting 2â&#x20AC;&#x201D;3 years (Houston 1975). Second, for birds in temperate areas, the seasons are marked and predictable. This leads to a single, predictable and rather short breeding season and, consequently, to a strict, regular organization of the annual cycle. Furthermore, in a highly seasonal environment, a favourable period after the breeding season is probably necessary for successful postfledging development before the onset of the cold period or migration. This provides a window in which the adults of most species can moult having no other major commitments and in which the energetic costs of moult may be minimal (as shown for Falco tinnunculus by Masman & Daan 1987). Alternatively, long-distance migrants may delay their complete moult until after reaching the winter quarters. In contrast, tropical species with prolonged breeding seasons have a less strict organization of the annual cycle and are more likely to moult slowly over a long and variable period of the year which occasionally includes part of the breeding season (e.g. Fogden 1972, Payne 1972, Foster 1974, 1975, Britton 1978). Birds with unpredictable breeding seasons have no strict annual cycle and may moult slowly over much of the year, including the breeding season, or may interrupt moult whenever the occasion to breed arises (e.g. Snow 1966, Keast 1968, Serventy 1971, Maclean 1973, Zann 1985, Thompson 1988). In such species, the moult strategy is less strict and less uniform within members of the species. Among European passerines, a tendency for variable moult strategies is apparent in the opportunistic breeder Loxia curvirostra (see p. 182) and in migrants wintering in tropical areas (see section 3.3.3â&#x20AC;&#x201D;3.3.5). On the other hand, tropical species under a regular and strong seasonal regime tend to have a well synchronized and distinct moult period after the breeding season like birds of temperate areas (Dowsett & Dowsett-Lemaire 1984). Thus, most European passerines have annual cycles with regular, distinct and relatively short, rather than prolonged and overlapping, periods for breeding and moult. Therefore, moult is comparatively intense and the costs more marked. These intense moults usually do not overlap significantly with breeding, migration and wintering and this has often been explained by the competition between moult and the other three events, notably for energy and nutrients (e.g. Stresemann & Stresemann 1966, Payne 1972). Despite the conflict between moult and breeding, overlap between the end of breeding and moult is widespread (see section 3.4.1) and various explanations for this have been proposed (e.g. Dhondt 1973, 1981, Foster 1974, 1975, Bensch et al. 1985; see section 3.4.1). Doubtless, a complicated set of trade-offs exists between the costs and benefits of moult, the features of the preceding breeding season (e.g.
6
The Function and Consequences of Moult
length of the breeding season, number of broods, clutch size, extent of parental care), the forthcoming autumnal activities (e.g. migration, territorial behaviour, food storage) and the prevailing environmental conditions (e.g. food availability and predictability, daylength, temperature, competition) (cf. section 3.4). Until now, only a few studies have looked more closely at these ecological interrelations. The temporal separation of flight feather moult and migration is rather strict (cf. section 3.4.1), except in some short-distance migrants and species which must maintain a high degree of flight capability all year round (e.g. hirundines). This may be due primarily to the conflict between moult and flight capability and between opposing metabolic adjustments for moult and (long-distance) migration (see section 1.3). In some species, it appears that autumn migration is endogenously timed very strictly and moult has to be finished by then (e.g. Tiainen 1981, Morton & Morton 1990, Underbill et ai 1992). Hence, if breeding is late, moult starts before the breeding season is over (see section 3.4.1). Most European passerines wintering in cold and temperate climates do not moult during winter/spring or, at most, renew only a few feathers. The few species which undergo a substantial prebreeding moult may, however, start before winter is over, despite the loss of insulation involved. Within a species, it appears that the timing, rate and extent of moult
can be adjusted according to a bird's individual circumstances (e.g. Dhondt & Smith 1980, Morton & Morton 1990, see also section 3.4). Within the time window set by the endogenous annual cycle and modified by the photoperiod (e.g. Gwinner 1986), the precise timing and rate of the postbreeding moult is thought to be fine-tuned by feedback from perceived environmental factors (e.g. food availability, temperature), social cues (e.g. breeding success, number of nestings, parental care, interactions between mates) and factors modifying moult once started (e.g. bad weather, unpredictable onset of breeding) (Palmer 1972, Payne 1972, Hahn et aL 1992). However, the actual role of many of these possible factors has not yet been convincingly demonstrated and the proposed hormonal mechanisms involved (summarized in Payne 1972, Hahn et aL 1992) certainly need to be further clarified. While research has shed some light on the timing and rate of the complete postbreeding moult (see above) and the partial postjuvenile moult (see section 4.4), the ultimate and proximate factors regulating prebreeding moult and seasonally divided moult strategies remain even more obscure. In particular, ecological and behavioural explanations of the timing, extent and rate of moult and their effects on other events in the life of a bird lag behind corresponding studies of reproduction. We hope that the detailed description of moult given in this book for many European passerines will provide a stimulus for this kind of study.
CHAPTER 2
The Terminology of Feathers, Plumages, Moults and Age Classes 2.1 Arrangement of the feathers In passerine birds, most of the feathers are contour feathers and these form the surface plumage of the full-grown bird and give it its shape and colour. They are grouped in distinct tracts (pterylae) which cover about half of the skin surface. The areas in between (apteria) are devoid of contour feathers and are usually hidden by the feathers of the adjacent pterylae. Contour feathers have closed vanes and little or no basal, downy (plumaceous) part. They vary enormously in size, shape and structure, within and among species, according to their specific function. A rough classification often used in moult studies distinguishes between two main types of contour feathers. Small feathers or body-feathers cover the head and body, while the term flight feathers includes the large feathers of the wing (primaries, secondaries and tertials) and tail (rectrices). The small feathers are reasonably symmetrical with almost equal vanes and a small proximal plumaceous part, while flight feathers usually have a narrow distal vane, a broader proximal vane and no plumaceous part. Associated with the flight feathers, and intermediate in structure, are the various wing-coverts, the alula and the tail-coverts. These are usually considered to be part of the small feathers. For the purpose of this book, we do not usually refer to the individual feather tracts of the body (see e.g. Clench 1970, Verbeek 1973, Morlion & Vanparijs 1979), but use a detailed classification of the feather rows of the wing and refer to them as feather tracts (see e.g. Zeidler 1966 and Morlion &: Vanparijs 1979 for a detailed description).
primaries which attach to the hand in those non-passerine species with nine or 11 primaries. It has been thought more practical for ringers, despite the difficulty of observing the reduced outermost primary. However, once familiar with the topography of the remiges, it will not be too difficult to find the innermost primary at the carpal joint by moving the wing, since the primaries move in a block. In any case, great care is needed when counting the primaries of moulting birds, especially at the start of primary moult when just the innermost primary is missing. It is important to state which system of numbering is used in every published observation since papers describing exceptional moult patterns are still presented without giving this vital information. The secondaries are numbered ascendantly (from outside to inside). In passerines, there are usually nine, but in some species ten or 11 secondaries. The six outer secondaries usually differ in shape and colour from the inner secondaries which cover most of the primaries and the six outer secondaries when the wing is closed. Those inner
2.1.1 Flight feathers The flight feathers of the wing are called remiges (singular remex). Those inserted on the metacarpus and the digits (hand or manus) are the primaries, those on the ulna (forearm) the secondaries and tertials (Fig. 8). Passerines have ten primaries (P). P 1-6 are attached to the metacarpus and P 7-10 to the digits (P 7 to the third digit, P 8-9 to the first phalange of the second digit and P 10 to the second phalange of the second digit). In some passerine species, the outermost primary is about half as long as the adjacent one (e.g. Troglodytes troglodytes), but in most species P 10 is very much reduced. In the Alaudidae, Hirundinidae, Motacillidae, Passcridac, Fringillidae and Emberizidae, P 10 is extremely small and difficult to detect under the primary coverts. The primaries are usually numbered descendantly, i.e. from inside to outside, towards the wing-tip (Ashmole et al. 1961, Stresemann & Stresemann 1966, Glutz & Bauer 1985, 1988, 1991, Cramp 1988, 1992, Cramp & Perrins 1993 and most other literature on moult), a convention which is followed in this book. This has the advantage that no difficulties arise with reduced outermost primaries and that the numbering corresponds to the normal sequence of primary moult which usually progresses descendantly. The ascendant system of numbering (from outside to inside) is used by some authors (e.g. Witherby et al. 1943, Vaurie 1959, Stephan in Bub 1985, Svensson 1992) and especially for indicating wing-formulae. The ascendant numbering preserves the homology of the four outermost
Fig. 8. Abbreviations and numbering of the feathers on the wing as used in this book, demonstrated by the wing of a 2y 9 Oenanthe oenanthe. MaC = marginal coverts. MeC = median coverts 1-8. GC = greater coverts 1-10. CC = carpal covert. Al = alula feathers 1-3. PC = primary coverts 1-9. T 7, T 8, T 9 = tertials 7-9. S = secondaries 1-6. P = primaries 1-10.
8
The Terminology of Feathers, Plumages, Moults and Age Classes
secondaries are called the tertials (T) and are usually not moulted in sequence with secondaries 1-6. In this book, we use the term secondaries (S) for the six outermost feathers only and always call the inner ones tertials, but give them numbers T 7 to 9. In European passerines, there are four or five tertials in the Alaudidae, Oriolidae and some members of the Corvidae (Stephan 1965, Stephan in Bub 1985). The Laniidae and Bombycillidae seem to have only three recognizable tertials (Svensson 1992, own observations), although they are reported to have four tertials by Snow (1967) and Stephan (in Bub 1985). Most passerines have six pairs of tail-feathers or rectrices (singular rectrix) (R). Among European passerines, only Cettia cetti has five pairs. They are numbered centrifugally from the inside to the outside.
2.1.2 Wing-coverts The gaps between the vane-less bases of the remiges are covered on both sides of the wing by the tectrices (singular tectrix) or coverts. On the upper side, the primary coverts (PC) are inserted just distally to each primary. PC 9 is very much reduced and covered by PC 8. PC 10 is extremely small, or absent. A greater covert (GC) is inserted just proximally to each secondary and tertial. An additional, innermost GC 10 has no corresponding tertial. Although counted with the greater coverts, GC 10 inserts at a slight angle, is often smaller than the adjacent greater coverts and is often moulted out of sequence with the other GC. It is debatable whether GC 10 is actually a true GC (Zeidler 1966). Above the greater coverts, there are eight to nine median coverts (MeC) and several rows of marginal coverts (MaC), the latter often called lesser coverts in many publications. However, it is a characteristic of passerines that the lesser coverts are absent or reduced to downy feathers (Wray 1887, Reichling 1915, Steiner 1917, Zeidler 1966, Stephan 1970). Between the primary and greater coverts lies the carpal covert (CC), a covert belonging to the carpal remex which is absent in passerines (Stephan 1974). The alula or bastard wing (Al) inserts at the first digit and consists of three feathers numbered from the smallest to the largest. They completely cover the very small median primary coverts. The underwing-coverts are not treated in this book (see e.g. Stubs 1972). They have been largely neglected in moult studies, except in a few cases on single species (e.g. Zeidler 1966, Winkler & Winkler 1985) and in the work by Rymkevich (1990) on a large number of European passerines.
2.2 Plumages, feather generations and moults 2.2.1 Concepts of moult and plumage terminologies Since most passerines of northern latitudes have distinct moult seasons which are intimately related to the annual cycle, a highly correlated sequence of plumages results among the members of a species or population which is relatively easy to describe in a nomenclature of plumages and moults. All plumage and moult terminologies currently in use originated from moult studies on the better studied birds of northern latitudes (e.g. Dwight 1900). However, passerines of tropical climates, opportunistic breeders and certain Palearctic migrants wintering in the tropics have moult periods and plumage cycles which are less or hardly related to the annual cycle or which exhibit a large variation among the members of a population (e.g. Stresemann & Stresemann 1966, Foster 1974, Britton 1978, Zann 1985, Thompson 1988, Loxia curvirostra p. 182, section 3.3). Such plumage and moult cycles are much more difficult to describe using the current terminologies. In non-passerines, the variation in moult and plumage cycles is so diverse that a convincing common nomenclature is quite impossible.
A terminology of plumages and moults could relate to the breeding cycle (e.g. postbreeding, postnuptial), to age and sexual maturity (e.g. juvenile, immature), to the season of the year (e.g. winter plumage), to the aspect of the plumage (e.g. eclipse plumage) or to a combination of these. A terminology unhindered by such relationships was introduced by Humphrey & Parkes (1959) and defines a key plumage or a key moult (usually the complete moult) from which homologous plumages and moults are derived (see also Rohwer etaL 1992). Most terminologies correlate easily for the simple plumage cycles of northern latitude passerines. Difficulties only arise when dealing with more complicated moult patterns and here each terminology has its own drawbacks (Humphrey & Parkes 1959, 1963, Stresemann 1963a, Amadon 1966, Rohwer etaL 1992, Willoughby 1992). The main difficulties with any terminology based explicitly or implicitly on homologies are that neither the phylogeny nor the genetics and control of moult and plumages are well enough known to determine homologies (Amadon 1966) and that it is necessary to know which parts of the plumage one single moult comprises. While we would accept the idea that the complete postjuvenile moult of Sturnus vulgaris is homologous to the partial postjuvenile moult of Erithacus rubecula^ there is, in our opinion, no sound basis on which to determine the homologies between the complete postbreeding and partial prebreeding moult of e.g. Motacilla alba and the partial postbreeding and complete prebreeding moult of Sylvia borin. Several species divide the moult of primaries and/or secondaries into two temporally separate phases. Thus, the two phases of flight feather moult may be regarded as one or as two moults. In the terminologies based on homologous moults and plumages, it is essential to know whether a feather renewal is merely the continuation of a suspended moult or a separate moult. While this question may easily be resolved for a primary moult (e.g. Anthus campestris), it is often much more difficult in secondary and body-feather moult (see section 3.3.3). In some species (e.g. Acrocephalus schoenobaenus)^ it is still not clear whether the complete moult in the non-breeding area is a separate moult or whether it is the continuation of the partial body-feather moult undertaken in the breeding area and perhaps even overlaps with a prebreeding moult. It is also conceivable that a moult split into two phases in a species' evolutionary history includes the renewal of some body-feathers during the second phase which have already been moulted during the first phase. The moult patterns of certain species of passerines (e.g. Sylvia warblers) and non-passerines suggest to us that the division of a formerly single moult into two temporally separate moults and the overlap of two formerly separate moults or moult waves may be more common evolutionary processes than hitherto recognized. A terminology based on homologies of plumages and moults would certainly be desirable and has many advantages (Humphrey & Parkes 1959, 1963, Rohwer et al. 1992). However, it would certainly require careful application, and should only be used for species whose moults and plumages have been specifically studied for homologies (e.g. Rohwer 1986, Thompson 1991, Young 1991) rather than just automatically replacing the existing descriptive terminology (e.g. Pyle et aL 1987). In our view, the means of identifying homologies with any degree of confidence is still weak for European species with complex moult patterns. Thus, adopting a general moult and plumage terminology based on the homology concept seems very premature and, for general descriptive purposes, we advocate the use of the more traditional terminology. The challenge for future specialist studies of moult will be to evaluate the phylogenetic homologies, functional adaptations and their various interrelations. Since we are dealing with passerines of temperate areas, a terminology which relates the plumages and moults to the life-cycle of the bird is appropriate. The breeding season is a distinct and convenient annual event and we have adopted the general terminology used by Roselaar (in Cramp 1988, 1992, Cramp & Perrins 1993; similar to Amadon 1966 with modifications) which relates the plumages and
Age classes
moults to the breeding cycle. However, unlike Roselaar (in Cramp 1992), we have usually named the moult of certain long-distance migrants before autumn migration the postbreeding/postjuvenile moult and all subsequent moults in the wintering area the prebreeding moult. Thus, we have kept the naming of moults strictly relative to breeding and the autumn migration to avoid uncertainties as to whether the moult starting in the breeding range is continued in the tropics or not.
2.2.2 General terms The term plumage refers to all the feathers normally covering a bird for an appreciable length of time (Amadon 1966). During moult, birds are in transition from one plumage to the next. The change from one plumage to the next can only occur by moult, not by feather wear changing the plumage appearance. Usually, only the contour feathers are taken into account. A plumage may be composed of one or several feather generations. Plumage is used similarly by Cramp (1988, 1992, Cramp & Perrins 1993) and many others and is included in the more broadly defined terms 'feather coat' and 'aspect' of Humphrey & Parkes (1959) and 'feathering* of Palmer (1972). The term feather generation designates the feathers acquired at a single moult, consisting of anything from only a few to all the feathers of a bird. Feather generation is defined similarly by Amadon (1966) and Palmer (1972) and equals the term 'plumage' as used by Humphrey & Parkes (1959). Moult is the natural replacement of feathers by a new feather generation. More than one feather generation may be replaced in one moult. A single moult may be discontinuous (suspended). However, because in many species it is not clear whether the second phase of an interrupted moult is really the continuation of the first, we often have to give the two parts of an interrupted moult different names.
2.2.3 Moult terms The first true feathers acquired by a nestling passerine bird constitute the juvenile plumage. Fledging defines the moment at which a feathered chick leaves the nest. The first moult after fledging, which replaces part of or the entire juvenile plumage, is the postjuvenile moult. In European passerines, this usually occurs during the first summer/autumn of a bird's life. Later moults start either before the breeding season in winter/spring or after the breeding season during late summer/autumn and are termed prebreeding moult and postbreeding moult, respectively. In many species, only one of these moults occurs, usually the postbreeding moult. Normally, the first prebreeding and postbreeding moults during the life of a bird are similar to later prebreeding and postbreeding moults, respectively. In certain species, however, they differ in extent or coloration of the feathers they produce and have to be explicitly termed first prebreeding moult and first postbreeding moult. Any of the above moults may be of very different extent. A moult comprising the whole plumage is termed a complete moult. We use this expression in a strict sense and not for cases in which a regular descendant primary moult began but was not finished with certainty. If, however, only one or a few individual feathers (e.g. a single alula feather, a few body-feathers or a single secondary) have been retained exceptionally, we would still call the moult complete. A single moult frequently does not involve the whole plumage and is then called a partial moult. Following Harper (1984), the phenomenon by which a moult stops before the whole plumage has been renewed is called moult interruption. This term and the related terms suspended and arrested moult have generally been used only for primary and secondary moult and, in order to prevent confusion, we retain this usage. Two different types of
9
primary and secondary moult interruption are recognized (King 1972, Harper 1984). In the case of suspended moult, the primary and/or secondary moult is subsequently resumed at the point of interruption. Thus, the suspension normally divides a single moult into two temporally separated phases. Those primaries and secondaries not moulted during the first phase of the moult are renewed later during the second phase. In the case of arrested moult, the next primary and secondary moult starts at the normal site of initiation or another site other than the point of interruption. Thus, an arrested moult cannot later proceed to completion and the subsequent moult is in fact a different moult entirely. In the case of eccentric primary moult, the renewal of the primaries starts not with the outermost or innermost primary, but with a central feather and is interrupted (see section 4.3.3). Usually the next primary moult starts at the normal site of mOult initiation (usually primary 1). Eccentric primary moult is still poorly understood and may comprise several patterns of primary moult including several directions of progression. Therefore, we do not know whether it is always an arrested moult, whether resumption at the point of interruption may occur or whether a divergent sequence may even produce a complete primary moult. We use the term moult limit to name the point where two feather generations meet within or between any of the feather tracts, since the terms moult interruption and arrested moult are reserved for primary and secondary moult interruption only. Within the feather tracts of the wing, moult may proceed in a descendant (from the body towards the wing-tip), ascendant (from the wing-tip towards the body), convergent (from both the body and the wing-tip towards the centre) or divergent (from the centre both towards the body and the wing-tip) sequence. For the rectrices, moult may be centrifugal (from the central pair of rectrices, R 1, towards the outside) or centripetal (from the outermost pair of rectrices, R 6, towards the centre).
2.2.4 Terms for plumages, feathers and feather generations After fledging, all passerines wear the juvenile plumage. If there are two moults annually, the bird is in its breeding plumage after the prebreeding moult and in its non-breeding plumage after the postbreeding moult. If there is only one moult annually, a special term is superfluous, though the plumage may be termed annual. For individual feathers or feather generations, we refer to the moult at which these feathers were produced, e.g. a greater covert formed during the postjuvenile moult is termed a postjuvenile greater covert, Since partial moult is a frequent phenomenon, the plumage of a bird is frequently compounded of two or even three feather generations, each acquired during a separate past moult. In order to designate plumages more precisely for the purpose of this book, we prefer to refer to the extent of the past or current moult instead of using the plumage terms of Cramp (1988, 1992, Cramp & Perrins 1993) outlined above: e.g. after partial postjuvenile moult, after complete postbreeding moult, in suspended postbreeding moult, in postjuvenile moult etc.
2.3 Age classes We use the age classification which refers to the calender year. Birds fledged in the breeding season of the current year (up to 31 December) arefirst-yearbirds (ly, EURING Code 3). Birds fledged in the previous calender year and now in their second calender year (from 1 January) are second-year birds (2y, EURING Code 5). 1 y/2y birds are usually recognizable up to the first complete moult, after which they are called adults (ad), i.e. birds fledged before the current calender year (EURING Code 4) and birds fledged before the previous calender year (EURING Code 6) but whose precise year of fledging is otherwise unknown.
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CHAPTER 3
The Moult of Adults 3.1 Introduction to the moult strategies In European passerines, moult does not overlap significantly with breeding, migration and wintering in cold and temperate climates (see section 1.4). Consequently, moult is restricted to two distinct periods, the first between the breeding season and autumn migration or the onset of winter, and the second during winter, either in late winter/spring for birds wintering in northern latitudes, or over an extended, sometimes subdivided, period corresponding to the whole northern winter in birds which winter in the tropics. While all adult passerines normally replace the entire plumage at least once a year, many renew part of, and a few the whole plumage twice annually (for cases of the renewal of some feathers three times a year see sections 3.3.1 and 3.3.5; for the occasional retainment of some feathers for more than a year see section 3.3.3). Among European passerines, there is considerable inter- and intraspecific variation in the extent, timing, duration and sequence of the individual moults. The number of yearly plumage renewals as well as their extent and partition between the two moult periods is referred to as a moult strategy. In the remainder of this section, a broad overview of the various categories of moult strategies is given, pending a more detailed account in section 3.3. The sequence of moult is often related to the moult strategy, and varies more in .European passerines than is often thought. It is discussed in section 3.2 as a prelude to the detailed consideration of the strategies themselves. The timing and duration of moult and ecological aspects of the partition and extent of moult are treated in section 3.4. Hitherto, four moult strategies have usually been recognized in passerines, based on primary moult only: complete moult before autumn migration or the onset of winter, complete moult after autumn migration, two complete moults annually and moult suspension during autumn migration (e.g. Stresemann & Stresemann 1966, Ginn & Melville 1983). However, a more realistic insight into the moult strategies can be had by considering the moult of the rest of the plumage as well. In particular, it enables a better understanding of die sometimes bewildering variation between members of the same species. Also, unusual moult patterns can be more easily understood as transitions between more frequently occurring moult strategies. The usefulness of considering the moult of all parts of the plumage for ageing birds has been recognized for some time and has led to a rough classification of moult according to season (summer or winter) and extent (partial, complete, suspended etc.) (e.g. Svensson 1992). Compared to the uniform moult strategies of species wintering in northern latitudes, those of long-distance migrants wintering in the tropics are extremely varied. The high mobility of these species makes observation and study of their moult strategies difficult and our knowledge of them is far from complete. In particular, it is often difficult to assess whether feather renewal observed during a certain period at a certain place is a distinct moult of its own or the continuation of one started earlier or elsewhere (see discussion in section 3.3.5). Hence, a comprehensive classification of moult strategies based on moult and plumage cycles is not feasible at this time. Instead, we base our classification on seasonal occurrence and on the extent of moult, and recognize the six moult strategies shown in Table 1. All sedentary and migrant European passerines which winter in cold and temperate climates, as well as about half of the long-distance
migrants, perform a complete moult between the breeding season and the autumn migration or winter. The majority do not moult again during winter/spring and undergo only a complete postbreeding moult (strategy 1). About one third of the species which perform a complete postbreeding moult in the breeding area renew part of or all of the body-feathers (and occasionally also the tertials and rectrices) again during winter/spring, and thus undergo a complete postbreeding moult and a partial prebreeding moult which does not include the remiges (strategy 2). The remaining four strategies include the renewal of extensive parts of the plumage during winter and occur only in birds wintering in the tropics. Long-distance migrants can find stable and favourable conditions for moulting in the tropics and take the opportunity to perform the main moult after the autumn migration (complete moult in the non-breeding area, strategy 3). This strategy is adopted by about one half of the long-distance migrants. They usually undergo a partial moult before autumn migration, which may be interpreted either as the beginning of the complete postbreeding moult achieved mainly in the non-breeding area or as a separate partial postbreeding moult (see section 3.3-2). Certain long-distance migrants moult part of the remiges before autumn migration and part during winter in the non-breeding area (seasonally divided moult of remiges, strategy 4). This strategy is proposed for the sake of simplicity and actually includes several rather different moult strategies which are detailed in sections 3.3.3 and 3.3.5. The seasonal partition of the moult of remiges may concern one single moult which is suspended, usually during autumn migration, or it may concern the postbreeding and the prebreeding moult, both being incomplete, but complementing each other. The majority of the plumage may be renewed before or after autumn migration, and the body-feathers, tertials and rectrices once or twice annually. The Table 1. The principal moult strategies of European passerines based on the seasonal occurrence and extent of their moults. Moult strategies of species with variable breeding seasons (e.g. Loxia curvirostm) are not included. Strategy 4 is heterogeneous and described further in sections 3.3.3 and 3.3.5. Moult during summer/ autumn (before autumn migration) Complete None
Strategy 1 .Complete postbreeding
Body-feathers only
Strategy 2 Complete postbreeding, partial prebreeding
Part of remiges
Complere
Part of remiges
No remiges
Strategy 4 Seasonally divided moult of remiges Strategy 6 Biannual complete
Strategy 5 Postbreeding arrested within remiges, complete prebreeding
Strategy 3 Complete in the nonbreeding area
12
The Moult of Adults
seasonal division of the moult of remiges is the normal strategy in only a few species. In many species, only a minority of the individuals follow strategy 4, the majority moulting according to strategy 1, 2 or 3. For moult research, the patterns subsumed in strategy 4 are of particular interest because they show that moult strategies are variable, not clearcut and mutually exclusive, and because they suggest ways in which moult strategies may have evolved. While birds moulting according to strategies 1-4 may renew only the body-feathers, tertials and rectrices twice annually, birds belonging to strategy 5 also renew part of the remiges twice a year (postbreeding moult arrested within remiges, complete prebreeding moult). This category includes species whose conspecifics moult mainly according to strategy 3 or 6, and thus may be regarded as representing a transition towards having two complete moults annually (biannual complete moult, strategy 6). Only two Palearctic passerine species perform two complete moults a year: Phylloscopus trochilus and Lanius cristatus. Two more are known to moult all their primaries and most of the other feathers twice a year: Lanius tigrinus and Pericrocotus divaricatus (PrysJones 1991; see section 3.3.4). Species with a very variable breeding season avoid, or at least slow down, moult during breeding and, consequently, cannot follow a fixed moult cycle (see section 1.4). They interrupt moult at various stages and this results in individually variable and sometimes complex moult patterns which are not covered by the moult strategies given above. The only such species treated in this book is Loxia curvirostra. We entirely omit this species from the following general account and refer the reader to p. 182. We also omit the peculiarities of the moult of Cisticola juncidis (see section 4.4,4),
3.2 Sequence of moult 3.2.1 Basic sequence of the complete moult Compared with non-passerines, the sequence of the complete moult of passerines is rather uniform between species and is referred to as the basic sequence (Ginn & Melville 1983). The complete postjuvenile moult follows the same sequence and is, therefore, included in this section. A full description of the moult sequence includes both the sequence within each feather tract and the relationships between feather tracts.
Flight feathers Within the flight feather tracts, the basic sequence is as follows (Fig. 9 and 10). The primaries are moulted descendantly beginning with P 1, the secondaries ascendantly beginning with S 1. The tertials follow their own sequence and are usually renewed in the order T 8-9-7. The rectrices are renewed in pairs, centrifugally, starting with R 1. Primary moult extends over virtually the entire moult period and is usually taken as a reference for the progress of moult in the other feather tracts. In an average bird, the renewal of the tertials and rectrices starts once primary moult has reached about P 4 (Fig. 9 and 10). Secondary moult begins during growth of P 5. The tertials and rectrices are full-grown by the time that P 8 and 9 are growing. Due to its small size, P 10 is usually full-grown before P 9 or P 8'. The last flight feathers to complete growth are usually S 5 and S 6. Normally, moult proceeds symmetrically on both wings.
Body-feathers and wing-coverts Moult of the body-leathers usually starts after the beginning of primary moult and often lasts longer than the renewal of the flight feathers. The
Fig. 9. Sequence of flight feather moult in a captive Pyrrhocorax gracu/us. The bars indicate the growth duration of individual flight feathers, divided into the growth of the web (white bar) and the final growth and keratinization of the calamus (or quill) which results in only a slight increase in feather-length (hatched bar). (After Winkler^/. 1988).
feathers on the head are normally moulted last. The greater and carpal coverts are shed soon after the start of primary moult and are well or almost full-grown before the secondaries are renewed (Fig. 10). The greater coverts are all shed at once, or in a variety of more complex patterns: e.g. within short intervals, descendantly in groups (e.g. Bahrmann 1964, Zeidler 1966, Mester & Prunte 1982, Alonso 1984), ascendantly (Rogge 1966, Dhondt 1973), convergently (Winlder & Winkler 1985)> in an ascendant and divergent wave (Dorka 1971) or divergently with a very variable focus around GC 4-5 (Kasparek 1979a). While the carpal covert is moulted in sequence with the greater coverts, GC 10 is not renewed until the other greater coverts are almost full-grown (Zeidler 1966, Kasparek 1979a, Alonso 1984, Winkler & Winkler 1985). The median coverts are renewed while the new greater coverts are growing, or are full-grown. The marginal coverts start moulting soon after P 1 is shed and are renewed throughout much of the period of primary moult. The alula and the underwing-coverts are replaced during the second half of primary moult. The primary coverts are renewed together with the corresponding primary, slightly earlier or later (Rogge 1966, Zeidler 1966, Kasparek 1979a, Winkler & Winkler 1985, Dittberner & Dittberner 1987). There is only limited variation in the moult sequence of the wing-coverts between species, but detailed descriptions are only available for a small number of European passerines (e.g. Sturnus vulgaris, Bahrmann 1964; Passer domesticus, Zeidler 1966; Erithacus rubecula, Rogge 1966; Pyrrhula pyrrhula, Newton 1966, 1967; Corvus frugilegus, Dorka 1971; Parus major, Dhondt 1973; Prunella modularis, Ginn 1975; Corvidae, Seel 1976; Emheriza schoeniclus, Kasparek 1979a; Passer hispaniolensis, Alonso 1984; Montifringitia nivaiis, Winkler & Winkler 1985; Pyrrhocorax graculus and P. pyrrhocorax, Winkler etai 1988).
3.2.2 Functional aspects of the basic sequence of moult Many aspects of the basic sequence of moult can be interpreted as functional adaptations. However, since no one has yet done a detailed study on the effects of wing-feather moult and its sequence on flight performance in passerines (cf. Daan 1982, Sylven 1982 and Tucker 1991 for
Sequence of moult
13
Fig. 10. Progress of the complete moult of the wing and tail, following the basic sequence. The progress of moult is represented schematically by ten stages (A-J), one for each primary to moult. The primaries (P), primary coverts (PC), alula feathers (Al), secondaries (S), tertials ( f)Âť greater coverts (GC), carpal covert (CC), median coverts (MeC) and marginal coverts (MaC) of the right wing as well as the right half of the rectrices (R) are represented by rectangles. The body of the bird lies at the left edge of each diagram. Old feathers are indicated in white, new feathers hatched, growing feathers in black and in thrir approximate length (the example species is Passer domesticus,, after Zeidler 1966, modified).
raptors, and Sach 1968 for Numenius arquatd) much that follows remains speculative. The primaries take the most time to be moulted, since they cannot be shed simultaneously without severely reducing the power of flight and because the daily growth rate of the individual primary is limited.
The body-feathers comprise about 70% of the total plumage mass (Newton 1966) and, consequently, require most energy and nutrients for replacement. Thus, it would be adaptive to spread both primary and body-feather moult over the entire moult period. The descendant replacement of the primaries is thought to provide a
14
The Moult of Adults
better protection for the growing primaries against upward bending by lift forces during flight, than the ascendant sequence (Noordhuis 1989). The secondaries are shorter, overlap more and are apparently less affected by aerodynamic forces. Secondary moult starts only after the innermost primaries are full-grown, thereby avoiding a widening of the gap during replacement of the innermost primaries. The protecting tertials and greater coverts are moulted, or at least well grown, before secondary renewal commences. Among the tertials, T 7 and 8 have the greatest protective function and their moult is separated in slow moulting passerines (e.g. Passer domesticus, Zeidler 1966; Corvus frugtlegus, Dorka 1971; Montifringilla nivalis, Winkler & Winkler 1985; Pyrrhocoraxgraculus and P. pyrrhocorax^ Winkler et al. 1988). The old median coverts protect the first stages of greater covert growth. They themselves are moulted under the protection of the newly grown marginal coverts. The primary coverts are shed together with the corresponding primary, but since the base of each primary is covered by the preceding proximal primary covert, a minimal protection of the primary pin is ensured, at least. The alula feathers are replaced during the renewal of the outer primaries while their function of stabilizing airflow over the outer primaries at high angles of attack is obsolete (Evans 1966). The rectrices are shed before the outer primaries, so that at least one of these sets of feathers, which are both important in landing, have no gaps during moult (Evans 1966). Many studies report that the speed of primary moult (measured by the increase in moult score, see e.g. Ginn & Melville 1983) slows after the shedding of the central primaries until all the primaries are fullgrown. This is mainly due to a gradual increase in the intervals between the shedding of adjacent primaries. In addition, in some species the growth rate of the two or three outermost primaries is less than that of the other primaries (e.g. Pyrrhula pyrrhula, Carduelis flammed, C. chloris, Newton 1967, 1969; Montifringilla nivalis, Winkler &: Winkler 1985; Corvidae, Seel 1976, Winkler et al. 1988). Thus, the outer primaries not only take longer to grow because they are longer than inner primaries, but also because they grow more slowly. In other species, the outer primaries grow as quickly as the inner ones (e.g. Passer domesticus, Zeidler 1966). The deceleration of primary moult is especially marked when tertials, rectrices and secondaries start moulting and, consequently, may be explained by metabolic constraints (e.g. Zeidler 1966, Spina & Massi 1992). However, the phenomenon also occurs in species with a long moult duration and, hence, low metabolic stress. Moreover, Muscicapa striata with its inverse moult sequence (see p. 138) also shows prolonged shedding intervals of the outer primaries, although few other feathers are growing at that time (Dorka 1971). A second explanation for decelerated moult of the outer primaries suggests that gaps among the outer primaries impair flight capability more than those among the inner primaries, and thus should be avoided, especially in species for which continuous flight capability is important (e.g. Corvus corax, Gwinner 1966). Dorka (1971) concludes that in Corvus frugilegus the second explanation is more likely, since the peak moult intensity of all remiges does not coincide with the time of least primary raggedness; therefore, the observed increase in shedding intervals is unlikely to be an immediate consequence of physiological constraints. In contrast, secondary moult usually starts with long shedding intervals. If the primaries are almost full-grown, secondary moult may speed up considerably, i.e. while shedding S 4-6 (e.g. Dwight 1900, Evans 1966, Newton 1966, Rogge 1966, Evans etal 1967, Dorka 1971, Seel 1976, Kasparek 1979a). This may be interpreted as a means of minimizing overall wing raggedness while the outer primaries are being replaced. In Corvus frugilegus, the secondaries are not shed simultaneously with the primaries, but in the intervals between primary loss, hence also minimizing wing raggedness. In addition, the intervals between shedding of the remiges are very constant between individuals, except for the intervals between P 5/6, P 9/10, S 1/2 and S 5/6. These
variable shedding intervals serve to re-coordinate primary with secondary moult and to accelerate the moult in late moulting birds (Dorka 1971).
3.2.3 Variations and exceptions to the basic moult sequence Primaries The moult sequence of the primaries is generally strictly descendant among European passerines. However, in a few individuals and species the focus of a complete primary moult may be shifted from P 1 to a central primary (divergent sequence) or to P 9 (ascendant sequence). Species normally showing the basic descendant sequence may exceptionally start with P 2 or P 3 (e.g. Garrulus glandarius^ Bahrmann 1971; Corvus frugilegus', Dorka 1971). A small proportion of Lanius cristatus show a divergent complete postbreeding or prebreeding primary moult starting with P 3, 4 or 5, while the majority exhibit the normal descendant sequence (Stresemann & Stresemann 1971). A considerable proportion of Locustella luscinioides moult the primaries divergently with a focus around P 4 (Steiner 1970, Mead &: Watmough 1976, Thomas 1977, Mtiller 1981, Trias et al. 1982, Bensch et al. 1991, own obs.), but normal descendant primary moult occurs also (Mtiller 1981, Stresemann & Stresemann 1970b, own obs.). Some Anthus richardi have been observed moulting from P 1 as well as from a central primary and may also show other irregularities (Stresemann & Stresemann 1968a). In all Muscicapa striata, the primaries are moulted ascendantly, but P 10 is usually shed only shortly before or after P 7 (Williamson 1960, 1972, Diesselhorst 1961, Stresemann 1963b). Birds known, or supposed, to renew part of their primaries twice a year follow an eccentric or ascendant sequence during the partial moult, so that the most exposed primaries are renewed twice a year. Eccentric primary moult has been observed exceptionally in Sylvia borin (P 1+8â&#x20AC;&#x201D;9 renewed, see p. 127), Sylvia nisoria (Hasselquist et aL 1988, Lindstrom et al. 1993) and Phylloscopus sibilatrix (Montalto 1988). Locustella fluviatilis regularly moults the outer one to five long primaries, and usually also P 10, in autumn before a complete moult in winter which follows the basic sequence (Pearson & Backhurst 1983). Judging from feathers with a sheath still visible at the base, these authors concluded that this partial primary moult follows an ascendant sequence. The moult of the alula occurs together with the outer primaries. Both the ascendant primary moult and the concurrent alula moult also occur in Muscicapa striata and it would be interesting to look in more detail at the moult patterns (especially those of the primary coverts) of these two species in order to see to what extent their peculiar moult patterns can be exactly correlated. In those species with a single primary moult each year, one or a few primaries may exceptionally be retained. This usually involves the last primaries to be moulted (P 9 or 10; e.g. Hirundo rustica, Anthus trivialis, Oenanthe oenanthe, Fringilla coelebs, Carduelis spinus> see part II), In Sturnus vulgaris, however, the remiges to be moulted last (the outermost primaries) or first (the innermost primaries since moult is eccentric) maybe retained (Schleussner etal. 1985, Evans 1986, Schleussner 1990, Meijer 1991); in the case of an eccentric primary moult, the suggested sequence is descendant according to Schleussner (1990), but ascendant according to Evans (1986). As far as is known, birds with a seasonally divided primary moult usually follow the normal descendant sequence and resume primary moult at the point of interruption (suspended primary moult; see section 3.3.3). However, Sylvia c. communis may retain some central primaries before the autumn migration and may show various irregular moult sequences (T. Fransson in lift., G. Nikolaus in litt.\ see p. 123 and section 3.3.3 for a possible explanation).
Sequence of moult
15
Fig. 12. Ficedula albicollis ad 6 after partial prebr moult, 12 May. MaC and MeC prebr. GC 1 postbr, 2—10 prebr. T prebr. S 1—4 postbr, 5—6 prebr. Rest of wing postbr. In certain species performing an extensive prebreeding moult which includes all tertials, the innermost secondaries may also be moulted.
Fig. 13. Percentage of individuals which have moulted a given tertial after completion of a partial moult, of those individuals (N) which have moulted at least one tertial (own data). The individuals are subdivided into those with all three tertials renewed (white), those with only one tertial renewed (hatched) and those with two tertials renewed (dotted). In all Motacillidae and in Phylloscopus collybita (prebreeding moult), adults and second-year birds are included. In Sylvia borin and Muscicapa striata (postbreeding moult) only adults are shown.
Fig. 11. Percentage of adults which have retained a given secondary after an otherwise complete moult (hatched) or have moulted a given secondary after completion of a partial moult (dotted), of those individuals (N) with at least one retained (hatched) or moulted (dotted) secondary. In spring birds Q£ Muscicapa striata, it is difficult to judge whether or not S 6 has been retained (cf. p. 139). Sources: Carduelis spinus, Ficedula hypoleuca, Emberiza hortulana, Sylvia c. communis spring: own data; Phylloscopus trochilus; Mead & Watmough 1976, Swann & Baillie 1979, own data; Sylvia c. communis autumn: Mead & Watmough 1976, Swann & Baillie 1979, T. Fransson in litt., own data; Sylvia nisoria: Hasselquist etal. 1988, Lindstrom et al. 1993; Muscicapa striata: Mead & Watmough 1976, Hansen 1985, Rymkevich 1990, own data.
Secondaries Exceptions to the normal ascendant sequence of a complete secondary moult are few, but frequent in partial secondary moult. In the course of a complete moult, a few individuals of many species may shed S 6 before S 5- The secondary moult of Locustella luscinioides may show a
variety of sequences (Steiner 1970, Thomas 1977, Miiller 1981). In Cinclus cinclus, the secondaries are moulted in a variable sequence, but S 6 usually before S 4 (Richter 1954, Stresemann & Stresemann 1966, Galbraith et aL 1981). Convergent secondary moult was found in all individuals of Muscicapa striata (Diesselhorst 1961, Stresemann 1963b, Williamson 1972) and Cisticola juncidis (sequence 1—2—6—3—5^; Gauci & Sultana 1981) and in 2.5% ofSturnus unicolor (Peris 1988). Species which normally renew all the secondaries during the complete postbreeding moult may exceptionally retain one or a few of the last secondaries (usually S 6 or S 5—6, e.g. Motacilla flava, Anthus trivialis, Fringilla montifringilla, Serinus citrinella> Carduelis flammea, see part II). Species in which a small percentage of the individuals retain one or a few secondaries during the postbreeding moult usually start with S 1, but may also renew S 6 in addition to the outer secondaries (9.3% of the individuals retaining at least one secondary in Carduelis spinus^ 7.0% in Ficedula hypoleuca^ Fig. 11). In Phylloscopus trochilus^ this percentage is about 40% (Fig. 11, cf. Norman 1991b) and in Emberiza hortulana, which usually retains part or all of the secondaries during the postbreeding moult, 23% moult S 6. Sylvia
16
The Moult of Adults
nisoria, which usually retains all or most of the secondaries, may moult S 1 or, if more secondaries are moulted, sheds S 1+2+6 almost simultaneously, followed by S 5, although other (irregular) sequences occur as well and rarely all the secondaries are moulted following the basic sequence (Hasselquist et al 1988, Rymkevich 1990, A. Lindstrom pers. comm.), In Sylvia communis, the moult wave starting at S 6 may regularly proceed further, resulting in a convergent sequence (Fig. 11). Long-distance migrants with a partial postbreeding moult including the tertials may, along with the tertials, also replace S 6 (e.g. Anthus campestris, Locustella naevia, Oriolus oriolus, Lanius collurio, see part II). Species which renew the secondaries during an extensive partial moult do not usually follow the basic ascendant sequence. During the partial prebreeding moult, the renewal of secondaries seems to proceed strictly descendantly in Ficedula hypoleuca (all birds which renewed at least one secondary moulted S 6, Fig. 11) and probably also in F. semitorquataand F. albicollis (Fig. 12, Roselaar in Cramp & Perrins 1993). A descendant sequence during the prebreeding moult was also observed in actively moulting Sylvia curruca (see p. 121). Other species which regularly renew tertials during the prebreeding moult may, along with the tertials, also replace S 6 (Anthus trivialis, A. spinoletta, Motacilla flava, Phylloscopus colly bita, see part II; Sylvia cantillans, own data). In Sylvia c. communis, the sequence during the prebreeding moult may be descendant, convergent or eccentric (31% renewed all the secondaries, 13% only S 6, 16% two to five innermost secondaries, 13% one or two innermost as well as one to three outermost and 3% one central secondary, N=39, own data). A study of actively moulting Sylvia nisoria in Kenya revealed that secondary moult usually proceeds convergently starting either with S 6 or S 5 and S 1 or S 2, but irregular sequences may occur as well (Hasselquist et aL 1988, Lindstrom et al 1993, A. Lindstrom pers. comm.). Hence, the central secondaries are moulted by most individuals, while the outer- and innermost may be retained (Fig. 11). The secondary moult of Anthus richardi may also show irregularities (Stresemann & Stresemann 1968a). Muscicapa striata may retain the central secondaries during the prebreeding moult and may moult some central secondaries during the postbreeding moult. To summarize, species retaining some secondaries during an otherwise complete moult have the tendency to moult their secondaries convergently, retaining the well protected central secondaries. During the complementary partial moult, the sequence may be either strictly descendant, convergent, eccentric or variable.
Tertials Although the most frequent sequence of the tertial moult is T 8—9—7, it is often varied (usually to 8-7—9), especially in species which shed them at short intervals. In those species which moult the tertials during the course of a partial prebreeding or postbreeding moult, T 8 is the most frequently moulted, in particular if only one tertial is renewed (Fig. 13). This suggests a divergent sequence within the tertials, although some individuals may renew only T 9 or T 7- In Motacilla, alba, individuals renewing only T 7 are relatively frequent. Motacilla flava usually moults all the tertials during the partial prebreeding moult, and the most frequent sequence is T 8-7—9 (Wood 1976), but the few individuals known to have renewed only one tertial all replaced T 7 (see p. 77). Rymkevich (1990) reports that Sylvia nisoria may renew only T 7 or T 7-8 during the postbreeding moult.
Rectrices During a complete moult, the rectrices may be shed almost simultaneously or in an irregular sequence (e.g. many individuals of Motacilla flava, M, alba, Anthus spinoletta, A, trivialis, A. richardi, Cinclus cinclus,
Fig. 14. Percentage of individuals which have moulted a given rectrix after completion of an extensive partial prebreeding or postbreeding moult, of those individuals (N) which have moulted at least one rectrix (own data). The individuals are subdivided into those with all six rectrices renewed, those with only one rectrix renewed, those with R 1 and R 2 renewed, those with R 1 and R 6 renewed and those with other combinations. In all Motacillidae and in Phylloscopus collybita (prebreeding moult), adults and second-year birds are included. In Sylvia borin (postbreeding moult) only adults arc shown.
Prunella modularis, Luscinia megarhynchos> L. luscinia, Oenanthe oenanthe, Turdus torquatus, Acrocephalus dumetorum, Regulus regulus, R. ignicapillus, Sturnus vulgaris, S. unicolor, Plectrophenax nivalis, Calcarius lapponicus), in a convergent sequence within each half of the tail (1-6-2-5-3-4, often modified: Motacilla alba, M. flava; Glutz & Bauer 1985), R 6 before R 1 (Motacilla cinerea) or R 6 before R 5 or R 4 (Hirundo rustica, Ptyonoprogne rupestris, Anthuspratensis). In the two Certhia species, R 1 is shed only after the simultaneously shed R 2-6 are well grown. As in woodpeckers, this can be explained by the importance of the supporting function of the tail (Stresemann & Stresemann 1966). In Muscicapa striata, moult of the rectrices proceeds centripetally from R 6 (Diesselhorst 1961, Stresemann 1963b,
Moult strategies Williamson 1972). A centripetal sequence is also found in some individuals of Sturnus unicolor (Peris 1988), while S. vulgaris may show nearly centripetal, alternating or irregular sequences (Bahrmann 1964, 1970). In the course of a partial prebreeding moult, the rectrices are usually renewed in the normal centrifugal sequence (e.g. Sylvia, borin and Phylloscopus colly bita, Fig. 14). Exceptions are again most frequent among the Motacillidae. Observations on birds whose prebreeding moult is completed (Fig. 14) suggest that rectrix moult usually starts with R 1. In Anthus trivialis, it is usually followed by R 2, rarely by R 6. In A. pratensisy A. spinoletta, Motacilla cinerea, M. alba and possibly A campestris (Stresemann & Stresemann 1968a), R 1 is usually or always followed by R 6, suggesting a convergent sequence within each half of the tail as Wood (1976) found in M. flava. In M. alba, R 6 may even be renewed on its own (Fig, 14). In Sylvia nisoria during the postbreeding moult, some individuals moult only R 1â&#x20AC;&#x201D;2, others R 1-2+5-6 (Rymkevich 1990).
Wing-coverts Few studies have investigated the moult sequence of the wing-coverts during a complete moult and, as described above, there appears to be some variation between species, especially in the greater covert moult sequence. During a partial moult, the greater coverts are usually renewed descendantly, except that GC 10 is generally out of sequence as in the partial postjuvenile moult (see wing schemes in part II). However, in some species, the greater coverts are often moulted in an irregular sequence (e.g. Motacilla flava, Sylvia borin, S. c. communis, S. cantillans).
Variation in the relationships between flight feather tracts During a complete moult, the relationship between the renewal of the flight feather tracts exhibits some variation within and among species. The most divergent patterns are shown by species which accelerate the primary moult by having five to seven primaries growing simultaneously and in which the innermost primaries are shed at very short intervals. In these species, the onset of secondary moult is delayed relative to primary moult. In Luscinia luscinia^ the innermost four primaries are shed within four days. S 1 is shed only after P 7, and S 2 only after P 9. The retained secondaries, therefore, form a functional part of the wing while up to seven primaries are growing simultaneously, and are mainly renewed after the primaries are grown (Berger 1967). In other species with rapid moults, up to six primaries are growing simultaneously and secondary moult starts when P 6 or P 7 is shed, but is finished together with or shortly after primary moult (Oenanthe oenanthe, Williamson 1957b; Plectrophenax nivalis, Stresemann & Stresemann 1970a, Green & Summers 1975; Calcarius lapponicus, Francis et al 1991). As in Luscinia luscinia, the moult of the remiges of Cinclus cinclus does not proceed successively, but in three phases during which the inner primaries, the outer primaries and the secondaries are shed, the secondaries being moulted in an irregular sequence (Richter 1954, Galbraith et aL 1981). However, the total moult duration is not reduced in this species (mean of 70 days for primary moult and 15 additional days to complete secondary moult; Galbraith et al. 1981). This peculiar pattern is probably an adaptation for underwater locomotion, for which it appears to be essential to maintain an uninterrupted surface to the wing (Galbraith et al. 1981). Motacilla alba spreads the moult of the rectrices over almost the entire duration of the primary moult, thus the function of the tail is less impaired than in other species (Jukema & Rijpma 1984). Birds which suspend primary moult maintain the basic relationship
17
between primary and secondary renewal, whereas birds interrupting secondary moult, but renewing all the other feathers, interrupt the shedding of the secondaries at an earlier stage than would be expected in relation to the stage of primary moult. It appears as though the number of secondaries to be retained is predetermined.
3.3 Moult strategies 3.3.1 Complete postbreeding moult in the breeding area: Moult strategies 1 and 2 Complete postbreeding moult in the breeding area The majority of European passerines, i.e. all the sedentary and migrant species which winter in cold and temperate climates, as well as some of the long-distance migrants, perform a complete moult between the breeding season and the autumn migration or the onset of winter (groups 1 and 2 in Table 2). This strategy has several advantages. The plumage is renewed after the season of most intense wear and during a warm period which usually provides predictable and high food resources which both allow successful postfledging development of the young and a period during which the adults have no other major commitments and can take time to fit in their moult. Birds wintering in cold and temperate climates can renew their plumage before the cold period when they will need good insulation and during which food availability is reduced or unpredictable. The maintenance of social hierarchies or winter territories and good powers of flight for hard weather movements also require sound feathers. Apart from Loxia curvirostra with its particular moult strategy, we know of no species wintering in Europe that delays its postbreeding moult into the winter. Resident birds of temperate regions generally have more time available for moulting than do migrants. Passerines breeding in the arctic and wintering in cold or temperate climates as well as those longdistance migrants moulting completely in late summer have to squeeze in moult between a late breeding season and an early autumn migration. Adaptations in timing and duration of the complete postbreeding moult in relation to the breeding season, migration and onset of winter are discussed in section 3.4.1.
Partial prebreeding moult About one third of the species performing a complete postbreeding moult in the breeding area renew part of the plumage again during late winter and spring (moult strategy 2, species see p. 59). The timing, extent and duration of this partial prebreeding moult are poorly documented. Migrants normally undergo this moult in the wintering area, but some may finish moult only during the spring migration (e.g. Anthus spinoletta, Herremans 1987; Motacilla flava, Serra 1992; Phylloscopus collybita, own obs.). In Anthus spinoletta (Herremans 1987) and Motacilla flava (Wood 1976), <$ moult earlier than 9 to coincide with their earlier spring migration. In many species, the partial prebreeding moult is restricted to a localized renewal of often conspicuously coloured parts of the plumage, such as the chin of Montifringilla nivalis, the throat of Luscinia svecica or head-feathers of Emberiza schoeniclus, Oenanthe pleschanka and O. hispanica. Other species replace part of the body-feathers and perhaps also some wing-coverts, tertials and rectrices (e.g. Delichon urbica, Oenanthe isabellina, O. oenanthe, Mediterranean Sylvia warblers, Phylloscopus collybita). Some wing-coverts, tertials and rectrices are regularly replaced in the Motacillidae, Saxicola rubetra, Ficedula
18
The Moult of Adults
hypoleuca, many Sylvia warblers and Acrocephalus melanopogon. In Motacilla flava, the prebreeding moult, which includes the bodyfeathers, tertials, rectrices and part of the wing-coverts (see p. 77), takes about 60 days (DJ. Pearson in lift,). In this species, many feathers of the head, throat and manrle are apparently moulted twice in the winter quarters, first during Novemberâ&#x20AC;&#x201D;early December when the cT become racially identifiable, and again during the extensive prebreeding moult during Januaryâ&#x20AC;&#x201D;March. Similarly, Anthus cervinus moults part of the head-feathers twice in the non-breeding area (Pearson & Backhurst 1973, DJ. Pearson in litt.). Trans-saharan migrants which perform a significant partial prebreeding moult related to a seasonally divided moult of the remiges are treated below (sections 3.3.2 and 3.3.3). For some species (e.g. Troglodytes troglodytes, Emberiza citrinella, Turdus merula, Carduelis spinus), it is unknown whether the occasional renewal of some body-feathers during winter and spring constitutes a distinct prebreeding moult or whether there are some body-feathers growing over much of the non-breeding season as suggested by Wetmore (1936). In others, the extent of the prebreeding moult is apparently variable and may be suppressed in some individuals (e.g. Cettia cetti, Sylvia sarda, S. undata, S. melanocephala, Glutz & Bauer 1991, Roselaar in Cramp 1992; Sylvia atricapilla, see p. 131; see sections 5.3.2 and 5.3.3). There are two possible reasons for performing a partial prebreeding moult: to effect a change in appearance or to replace worn feathers. The former is the more plausible explanation in those species which replace cryptic feathers with conspicuous ones (e.g. Motacilla. spp.^ Luscinia svecica, Oenanthe spp., Saxicola rubetra, Ficedula spp., Montifringilla nivalis, Emberiza schoenidus). Although the extent of the prebreeding moult is similar in both sexes, the resulting change in appearance is normally more striking in <S than in 9 . However, there have been no detailed studies on the effects of plumage changes due to the prebreeding moult on sexual and aggressive behaviours in European passerines. Furthermore, moult is not the only way in which the appearance of a bird may change. Many species become more conspicuous through the abrasion of cryptic feather fringes which reveal the otherwise bright feather (e.g. Phoenicurus phoenicurus, many Fringillidae, Sturnus vulgaris). In some species, the breeding plumage is attained by the action of both moult and abrasion (e.g. Emberiza schoenidus}. Some species which perform a partial prebreeding moult do not change their appearance very much, at least not to the human eye (e.g. Anthus trivialiSy A. pratensis, Phylloscopus collybita). Feather wear may be their reason for renewing certain feathers twice a year. Wear affects different feathers differently and is influenced by climate, habitat and season. One would expect feather replacement twice a year in those feathers which are most exposed and in those species which live in dense, hard vegetation (grass, sedges, reed, thorny scrub). In the Motacillidae, the inner greater coverts, the tertials and the rectrices are the most exposed and these feathers are, indeed, replaced much more regularly than the median and marginal coverts. This is in contrast to the postjuvenile moult, which generally includes all the median and marginal coverts, but only occasionally the tertials and rectrices, and hence predominantly replaces the loosely textured, small juvenile feathers. The convergent sequence of rectrix moult (see section 3.2.3) may also be interpreted as an adaptation to replace at least the most exposed rectrices R 1 and R 6. Replacement of worn feathers might also be a reason for the prebreeding moult of the Sylvia warblers and Acrocephalus melanopogon which skulk in dense, hard vegetation. However, the most exposed feathers are often also those which are the most conspicuous on a sitting bird, so that it is often impossible to rule out the importance of maintaining or changing plumage appearance. In summary, it remains difficult to explain why some species perform a partial prebreeding moult while others do not. In an extensive prebreeding moult, there is a possible trade-off between the costs in energy and nutrients as well as plumage impairment during moult on
the one hand, and the benefit of a profound change in appearance and the replacement of worn feathers on the other. However, the moult of only a few conspicuous feathers entails very small costs. The occurrence of a prebreeding moult may also be linked with phylogenetic relationships since it occurs predominantly in certain taxa: e.g. all members of the Motacillidae and Muscicapidae, most members of the Sylviidae and Emberizidae, but not in the Alaudidae, Paridae, Certhiidae, Corvidae and Fringillidae. Only in the Turdidae are there many species both with and without a prebreeding moult.
3.3.2 Complete moult in the non-breeding area: Moult strategy 3 The moult strategies considered here and in the following two sections (moult strategies 3-6) occur only in long-distance migrants which winter in the tropics. Their moult strategies show large inter- and intraspecific variations, but are often only poorly documented. Since the most detailed information is available from birds observed wintering in Africa, we shall concentrate here on these species and largely exclude those wintering in tropical Asia. Table 2 summarizes the literature and our observations dealt with in part II of this book. It is arranged similarly to Table 1, but dwells especially on the heterogeneous moult strategy 4. About half of the trans-saharan migrants moult completely in the non-breeding area during the northern winter (moult strategy 3; group 10 in Table 2). This complete moult usually follows the basic sequence (except in Muscicapa striata, see section 3.2.3 and p. 138) and may be temporarily suspended within Africa. Most individuals perform a partial moult before the autumn migration, and some appear to perform an additional partial moult after the complete moult in the non-breeding area.
Partial moult before autumn migration Prior to migration, most birds in group 10 (in Table 2) moult part of the body-feathers, rarely some wing-coverts, tertials and rectrices in the breeding area, while others (e.g. some individual hirundines, see part II, some Acrocephalus palustris and Lanius collurio, Rymkevich 1990; some Hippolais icterina and H. polyglotta, Roselaar in Cramp 1992) may not moult at all. Sylvia borin, Muscicapa striata, Oriolus oriolus, Lanius senator and L, i. isabellinus perform a more extensive moult of the body-feathers, wing-coverts, tertials and rectrices before the autumn migration. Acrocephalus palustris has an extensive moult of body-feathers in NE Africa during late autumn, then migrates to southern Africa where it performs a complete moult, including the recently renewed body-feathers (Pearson 1982, 1989 and in litt., Dowsettâ&#x20AC;&#x201D;Lemaire & Dowsett 1987). Other species might also continue to moult body-feathers during the course of a partial moult after their arrival at a first staging area in Africa and before their complete moult (e.g. Hippolais icterina, Locustella naevia\ Roselaar in Cramp 1992), but this requires further investigation.
Suspension of the complete moult within the non-breeding area Some species are known to suspend their complete moult during their stay in Africa (group lOa in Table 2). In Nigeria, Acrocephalus schoenobaenus may suspend primary, and rarely secondary, moult during unfavourable periods and resume it later (Aidley & Wilkinson 1987). Suspended primary and secondary moult of A. schoenobaenus has also been observed in N Ghana, Malawi and E Africa, and may be related to a southward migration within Africa (Hanmer 1979, Pearson
Moult strategies
19
Table 2. The present knowledge of moult patterns of European passerines wintering in subsaharan Africa arranged according to seasonal occurrence and extent. Species wintering mainly outside subsaharan Africa are not included. The table is arranged similarly to Table 1, but describes moult strategy 4 in particular detail. The groups belonging to the moult strategies of Table 1 are framed by thick lines. A few additional cases of particular moult patterns as well as moult cycles of birds belonging to moult strategy 3 are discussed in section 3.3. Moult during summer/autumn in the breeding area Complete
Complete except secondaries
Part of primaries
Secondaries
No remiges
Moult strategy 1
None
Group 1 "Luscinia luscinia 3 "Luscinia megarhynchos 3 "Phoenicians phoenicurus 3 Moult strategy 2
Bodyfeathers
Secondaries
Group 2 -Anthus campescris 4 "Anrhus rrivialis 5 'Motacilla flava 5 "Luscinia svecica 4 *lrania gutturalis 4 'Saxicola rubecra 4,5 "Oenamhe isabcllina 4,S "Oenamhe oenanihc 4,5 "Oenanthe pleschanka 4 "Oenanthe hispanica 4 "Oenamru.' dt.-si.Tii 4 "Monticola saxatilis 4 "Sylvia t.communis 5 "Sylvia curmca 5 •* Sylvia cantillans 4,5 -t-Sylvia hortensis 6 "Sylvia melanoccphala 4 'Sylvia rueppelli 4 "Sylvia conspitillata 4 "Fictfdula hvpolcuca ^ -Ficedula albicollis 5 -Emberi/a hortulana S "F.mht*ri7a rafsi.i (i Group 3 -Svlvia communis 5 -Svlvia curmca 5 + Fic(. p dufa hypoleuca ^ -fFicedula albicollis 5 + Fi«dulit semiiorquaia 5
Key * most or all individuals of a species + many individuals of a species - few individuals of a species . exceptional Moult of 1 body-feathers in rhe breeding area 2 body-feathers, tertials and rectrices in the breeding area 3 no prebreeding moult 4 body-feathers in the non-breeding area (prebreeding moult) 5 body- feathers, tertails and rectrices in the non-breeding area (prebreeding moult) 6 prebreeding moult controversial, not, or onlv poorlv known 7 Some individuals moult primaries eccentrically 8 A few individuals renew only some secondaries in the non-breeding season, thus keep some for 1.5 or 2 years
Group 4 .Anthus irivialis 5 +Sylvia cantillans 5 ^Svlviac.communis, icierops 5,8 -Svlvia curruca 5 "Svlvia nisoria 5,8 -Ficedula hypoleuca 5,8 "Emberiza hortulana 5
Moult strategy 4
Group 5 -Riparia riparia 1,2,4? -Hirundo rustica 1,2,3 -Delichon urbica 1,2,4 'Ambus campestris 1,2,4 .Sylvia cantillans 1,2,4,5 +Sylvia c.communis, icterops 1,2,5 - Lanius senator 1,2 .Muscicapa striata 1,2,5
Part of primaries
Group 6 + Muscicapa striata 1,2 .Sylvia borin 2 -Oriolus oriolus 1,2
Complete except secondaries
Moult strategy 6 Group 7 •Phy"»«--opasrroL-riilus
Moult strategy 3
Moult strategy 5 Group 8 -Phvlloscopus trochilus
Group 9a -Sylvia borin 1.2,7 -Lanius collurio 1.2
Group 10 "Riparia riparia 1.2,4? "Hirundo ruscica 1,2,3 "Detichon urbica 1,2,4 "Cercotrichas galactotes 1 "Locustella naevia 1,2 -Locustella luscinioides 1? 'Acrocephalus paludicola 1,2 'Acrocephalus palustrisl "A. scirpaceus 1,2,4 "A. schoenobaenus 1,2,4,5 "A. arundinaceus 1.2,4 -Hippolais iccerina 1 "Hippolais pallida 1 "Hippolais polvglotta 1 'Hippolais caligata 1 'Hippolais olivetorum 1
Group 9b 'Locustella fluviatilis 1
Complete
Group 1 1 + Locustella luscinioides .Sylvia borin .Uniiisrnllurio Unknown
Group 12 -Irania gurturalis 4 +Svlvia hortensis 6 "Lanins senator nilnricus fi -Emberiza caesia 6 +Lanius nubicus 6
Group 13 -Irania gutturalis 4 -Locustella naevia 1,2 +Locus[ella luscinioides 1,2,7 -Acrocephalus arundinaceus 1,2,4 -Sylvia hortensis 7? -Phvlloscopus bonelli 1,2 .Phylloscopus stbilarrix 1,2,7 .Oriolus oriolus 1,2 "I^nius nubicus 6
Group 14 .Locustella naevia 1,2 -Phylloscopus bonelli 1? .Lanius collurio 1 ,2
"Sylvia communis icterops 1,2 'Sylvia borin 1,2 +Sylvia cantillans 1,2 "Phylfoscopus bonelli 1,2 "Phvlloscopus sibilatrix 1,2 "Muscicapa striata 1,2 "l^anius collurio 1,2 "Lanius senator senator 1,2 "Lanius minor 1 "l.antus isabellinus 2 Group lOa .Acrocephalus palustris 1 -A. scirpaceus 1,2,4 +A. schoenobaenus 1,2,4,5 .A. arundinaceus 1,2,4 -Hippolais olivctorurn I
20
The Moult of Adults
etal 1979, Renschetal. 1991, Fig. 15, see section 3.4.2). Interruption and resumption of the primary moult was also observed in some A. scirpaceusandA. arundinaceus (Pearson 1973, Hanmer 1979, Bensch etaL 1991). Some Hippoiais olivetorum commence the primary moult in NE Africa and move further south while actively moulting the inner primaries (Pearson & Backhurst 1976). A very few, late passing A. palustris renew some innermost primaries in NE Africa, then migrate on to southern Africa (Pearson 1982 and in litt.) and so might also show a suspension of the primary moult within the non-breeding area.
area. In the second case that the postbreeding moult starts before the autumn migration, is suspended, and then resumed in the nonbreeding area, sometimes supplemented by a partial prebreeding moult later on. In many species both the extent of the moult in the breeding area and the detailed pattern of the moult in the non-breeding area are poorly known. On present knowledge, an extensive moult in the breeding area (e.g. Sylvia borin, Lanius i. isabellinus) probably represents a distinct partial postbreeding moult and the moult in the nonbreeding area a complete prebreeding moult, since the feathers renewed during the partial moult in the breeding area seem to be moulted again within the basic sequence of the complete prebreeding moult in the non-breeding area. Acrocephalus palustris performs a partial postbreeding moult at a first staging area in NE Africa, which may already have started in the breeding area, followed by a complete prebreeding moult later on. According to this interpretation, the occasional renewal of some of the innermost primaries in NE Africa would represent the beginning of the prebreeding moult. In the hirundines, however, it seems reasonable to assume that the postbreeding moult which starts with some body-feathers (and occasionally some primaries, see section 3.3.3 and part II) in the breeding area is suspended during migration and resumed in the non-breeding area. In Delichon urbica, and probably also in Riparia riparia, its last stages overlap with a partial prebreeding moult in Africa (see part II). Similarly, in many of the Acrocephalus and Hippoiais warblers, the complete moult in Africa could also represent a delayed complete postbreeding moult already started in the breeding area. Some of these birds perform an additional partial prebreeding moult. Further studies on the renewal of the small feathers are needed to show whether moult strategy 3 actually comprises three different moult cycles: (a) partial postbreeding and complete prebreeding moult, (b) postbreeding moult started in the breeding area and achieved mainly in the non-breeding area, (c) as (a) or (b) plus a partial prebreeding moult. Suspension of the complete moult within Africa and of the partial moult during the autumn migration adds variants to these moult cycles.
Additional prebreeding moult
3.3.3 Seasonally divided moult ofremiges: Moult strategy 4
There are indications of an additional, partial prebreeding moult including the body-feathers and wing-coverts, rarely some tertials and rectrices, taking place in the non-breeding area after the complete moult for Delichon urbica, Riparia riparia> Locustella • luscinioides, Acrocephalus schoenobaenus, A. arundinaceus, A. paludicola and A. scirpaceus (Pearson 1971, 1973, 1975a, Hanmer 1979, Aidley & Wilkinson 1987, Roselaar in Cramp 1992, DJ. Pearson in lift., part II). For A schoenobaenus and A. scirpaceus, this moult seems to occur in those individuals which moult completely during the early winter, in the northern part of the Afrotropics, but not in those which moult completely later on during the winter, further south (Pearson 1973, Roselaar in Cramp 1992; cf. section 3.4.2 and p. 118).
Seasonally divided primary moult
Fig. 15. Acrocephalus schoenobaenus 2y/ad after complete prebr moult which has been suspended within the primaries in the non-breeding area, 5 May. This bird suspended primary moult after the renewal of P l^t and resumed it later. P 1—4 are more bleached than P 5—10. S 1—6 were probably replaced during the course of the moult of P 5-10. The tertials and wing-coverts are difficult to assign. These feathers may have been moulted together with P 5—10, or later during a separate moult of body-feathers, except for the conspicuously older GC 1-2.
Conclusions It appears that trans-saharan migrants moulting completely in Africa may moult before autumn migration in Europe (a partial moult), in the northern Afrotropics (a partial or complete moult, or a complete moult suspended) and further south (a complete or partial moult). There is much inter-, but also intraspecific variation in the moult strategy. The question is whether the partial moult before the autumn migration represents a separate moult or whether it is the beginning of the complete moult carried out mainly in Africa. In the first case, the interpretation would be that of a partial postbreeding moult in the breeding area followed by a complete prebreeding moult in the non-breeding
Among the various seasonally divided moult patterns, suspension of the primary moult has been known for a long time, mainly from nonpasserines (e.g. Stresemann & Stresemann 1966). The complete moult starts in the breeding area, where some of the primaries are moulted, is suspended during the autumn migration and resumed at the point of interruption in the non-breeding area, thus conserving the basic sequence throughout (complete postbreeding moult suspended within primaries, group 5 in Table 2). Primary moult suspension is the normal strategy in Anthus campestris and A. richardi (Stresemann & Stresemann 1968a, own obs.), while a small percentage of both species perform a complete moult in the breeding area. Furthermore, primary moult suspension occurs regularly in a considerable proportion of Sylvia communis icterops (which normally moult completely in the nonbreeding area), in a small percentage of S. c. communis and Hirundo rustica (the first normally moulting completely in the breeding, the second in the non-breeding area), rarely in Riparia riparia, Delichon urbica, Muscicapa striata and Lanius senator? which normally moult completely during the winter, and in Sylvia cantillans (Sylvia communis and hirundines see part II; S. cantillans, Dowsett 1971; Muscicapa striata, Mead & Watmough 1976; Lanius senator, Svensson 1992). Birds in spring with clear signs of primary moult resumption (inner primaries older than outer; Delichon urbica, Fig. 63; Sylvia communis, see p. 124; S. cantillans, own obs; Anthus campestris, Fig. 70) confirm that the postbreeding moult has been suspended. All of these species,
Moult strategies except perhaps Hirundo rustica and Riparia riparia, renew at least some body-feathers, and sometimes some wing-coverts (Anthus campestris) and tertials (Sylvia communis, S. cantillans) twice a year, thus performing a partial prebreeding moult. Adult Sylvia c. communis which interrupt the primary moult before autumn migration, may retain the central primaries and thus show irregular moult sequences (T. Fransson in //#., G. Nikolaus in litt., see p. 123). There are no data on the subsequent moult of such birds in Africa. Since only second-year birds, and no adults, occur in spring with a complementary primary moult pattern (see p. 124), the moult of the inner and outer primaries during the postbreeding moult could be interpreted as being the completion of an eccentric primary moult which took place during the first prebreeding moult. In this case, the incomplete moult of the primaries during the postbreeding moult would not constitute the suspension of a normal postbreeding moult, but rather be a complementary facet of the foregoing first prebreeding moult, similar to a seasonally divided secondary moult (see below and section 3.3.5).
Seasonally divided secondary moult Birds which interrupt moult within the secondaries (groups 3, 4, 6, 12, 14 in Table 2) show rather variable and often complicated moult patterns. Two main types may be distinguished: birds which moult almost completely in the breeding area (groups 4 and 12) and those moulting almost completely in the winter quarters (groups 6 and 14). Group 4 comprises birds which undergo an extensive postbreeding moult in the breeding area, but which retain all or part of the secondaries, and occasionally some wing-coverts, tertials and rectrices (Sylvia nisoria, Hasselquist et al. 1988, Rymkevich 1990; S. communis, S. curruca, Ficedula hypoleuca> Emberiza hortulana see part II). In the nonbreeding area, these birds perform an extensive partial prebreeding moult which includes some or all of the wing-coverts, tertials and rectrices, and usually also renewal of some or all of the secondaries (postbreeding moult interrupted within secondaries, partial moult in the non-breeding area including secondaries, group 4 in Table 2, Fig. 16). As shown in section 3.2.3 for Sylvia nisoria, S. communis and Ficedula hypoleuca, the moult sequence of those secondaries lost in the
Fig. 16. Sylvia nisoria ad after partial prebr moult, 30 May. MaC mostly prebr. MeC prebr or postbr. GC 1+4 postbr, rest prebr. CC probably postbr. Al 1 prebr, 2â&#x20AC;&#x201D;3 postbr. P and PC postbr. T and S 1-6 prebr. Adult Barred Warblers moult their primaries during the postbr moult in the breeding area together with all the tertials, part or all of the body-feathers, part of the wingcoverts, usually the inner rectrices and occasionally one or a few secondaries. During the prebr moult in Africa, they moulr most or all of the secondaries, all the recrrices and tertials and apparently part of the wing-coverts and bodyfeathers, but only rarely single primaries.
21
breeding area is ascendant or convergent, while secondaries moulted in the non-breeding area are renewed in a variety of sequences (usually descendant or convergent). Hence, the renewal of the secondaries in winter proves not to be a clear resumption of the postbreeding moult. The two partial secondary moults seem either to be indiscriminately interlaced or the secondary moult is shifted entirely to the prebreeding moult. Indeed, some of the secondaries retained during the postbreeding moult are occasionally not renewed in the non-breeding area so that they have to last for one and a half or two years (S. nisoria^ Hasselquist et aL 1988; S. communis Fig. 343, F. hypoleuca Fig. 417). On the other hand, some secondaries may be moulted twice a year (complete postbreeding moult, partial prebreeding moult including secondaries, group 3 in Table 2). The fact that first winter individuals of these species start renewing their secondaries during the first prebreeding moult in winter (see section 4.6.3) suggests that winter replacement of the secondaries prepares them for possible retention in the following postbreeding moult, and does not represent a resumption of a secondary moult suspended during autumn migration as in the case of a suspended primary moult (Hasselquist et al. 1988, Lindstrom et al. 1993). Emberiza hortulana might differ from the other species of group 4; the first winter birds examined did not renew any secondaries in Africa (see p. 195), and the secondary moult during winter may often be a resumption of the suspended secondary moult started in autumn. The moult strategy of the birds in group 4 (Table 2) shows additional features which are difficult to interpret at present and which are not presented explicitly in Table 2. In spring, Sylvia nisoria, S. cantillans and S. c. communis may show differently worn wing-coverts within the same wing (own obs., p. 124). It is not yet clear whether they have been moulted at different times during a protracted prebreeding moult or whether there is an additional, possibly overlapping, moult (cf. Roselaar in Cramp 1992 and p. 124). In Sylvia nisoria, some adults retain P 10 during the postbreeding moult (Rymkevich 1990) and others were found to have renewed the outer primaries during the prebreeding moult in Africa (Hasselquist et al. 1988, Lindstrom et al. 1993). Rarely, some adults renew all the secondaries in the breeding area (Rymkevich 1990), thus possibly performing a complete postbreeding moult. A postbreeding moult interrupted within the secondaries is found in several other species (group 12 in Table 2). In most, it is likely that the retained secondaries are moulted in the non-breeding area in the course of a partial prebreeding moult (although caged Sylvia hortensis did not; Berthold & Querner 1982a), thus they might actually belong in group 4. A moult pattern related to group 4, but seasonally reversed, is shown by some Muscicapa striata and Oriolus oriolus (see part II). These birds perform an almost complete moult in Africa, during which they may retain some secondaries, and a partial postbreeding moult of limited extent in Europe, where they may replace some secondaries (prebreeding moult interrupted within secondaries, partial postbreeding moult including secondaries, group 6). It is not known whether or not the two moults are actually complementary. Similarly, a few Sylvia borin moult one or a few secondaries in the breeding area. Since spring birds with old secondaries have been observed, it is possible that these feathers are retained during the prebreeding moult (seep. 128). Some Phylloscopus bonelli have also been found with partially renewed secondaries in the autumn, but with the other remiges unmoulted (Mead & Watmough 1976) and very likely also belong to group 6, although it is not known whether or not these secondaries are moulted again during the prebreeding moult. Occasionally, Lanius collurio and Locustella naevia may be found with renewed innermost secondaries in autumn (Swann 6c Baillie 1979, p. 154, Fig. 17), but it is not known whether these feathers are renewed again during the prebreeding moult (group 14 in Table 2). A few Acrocephalus schoenobaenus and Phylloscopus sibilatrix were observed with old secon-
22
The Moult of Adults
Fig. 17. Locustella naevia ad after partial postbr moult, 1 September. MaC mostly prebr, MeC and GC mostly postbr. T postbr. S 1â&#x20AC;&#x201D;5 prebr, 6 postbr. Rest of wing prebr. This bird had also renewed the whole body-plumage and R 1-6, Some long-distance migrants with a complete prebr moult in the nonbreeding area may previously perform a rather extensive postbreeding moult in the breeding area. It remains unknown whether or not the feathers renewed in Europe are moulted again in Africa.
Fig. 18. Phylloscopus sibilatrix 2y/ad after an almost complete prebr moult, 28 April. Whole wing prebr except S 5. The feather generation of S 5 cannot be assigned. It may be a juvenile feather (in this case the bird is a 2y), a feather from the last complete prebr moult a year earlier or even a feather renewed in the course of the partial postbr moult during the foregoing summer. daries (mostly S 5, once S 1â&#x20AC;&#x201D;2 and S 2) in spring (own data, Fig. 18, not included in Table 2). Whether or not this is related to a postbreeding moult including the secondaries is also unknown.
3.3.4 Partial and complete biannual moult of remiges: Moult strategies 5 and 6 A few individuals of Sylvia borin and Lanius collurio have been found to renew some primaries in the breeding area. They most likely renew them again in the non-breeding area, in the course of a complete moult later on (postbreeding moult arrested within primaries, complete prebreeding moult, group 9a), since no spring birds have been found showing signs of primary moult resumption. The large number of S. borin examined in the spring tends to confirm this interpretation (see p. 128). Only a few spring individuals of L. collurio were, examined, but a moult of this type would make them comparable to other shrikes which also have an extensive postbreeding and a complete prebreeding moult (see Stresemann & Stresemann 1972a).
Locustella fluviatilis moults the outer one to five (usually three) long primaries, part or all of the alula feathers, tertials> greater, median and marginal coverts in NE Africa, then migrates further south where it performs a complete moult (Pearson & Backhurst 1976, 1983, Tucker 1978). This species carries out both the postbreeding moult arrested within primaries and the complete prebreeding moult in the nonbreeding area (group 9b in Table 2) and may start the postbreeding moult in the breeding area, if the renewal of some body-feathers by some individuals in the breeding area is interpreted as the beginning of the partial moult (Glutz & Bauer 1991, Roselaar in Cramp 1992). There are records of a number of species renewing some primaries in the breeding area (postbreeding moult interrupted within primaries, group 13 in Table 2; Williamson 1968, Mead & Watmough 1976, Thomas 1977, Montalto 1988, Spina 1990, Nikolaus & Pearson 1991, Roselaar in Cramp 1992), but it has never been shown whether they belong to group 5 (suspended primary moult) or group 9a (arrested primary moult). Adult Locustella luscinioides have been shown to renew only the central or outer primaries (Thomas 1977). Similarly, some Locustella certhiola and L. lanceolata, wintering in tropical Asia, have been found with renewed outer primaries in the autumn, although it is not known whether or not such birds renew the outer primaries again during the prebreeding moult, like L. fluviatilis (Glutz & Bauer 1991, Roselaar in Cramp 1992). Only one trans-saharan migrant, Phylloscopus trochilus, regularly performs two complete moults each year (biannual complete moult, group 7). One other Palearctic passerine, Lanius cristatus, shows a similar moult pattern, but the complete postbreeding moult may be suspended during autumn migration or may occur after leaving the breeding grounds. Furthermore, this species may show divergent complete primary moult, arrested primary moult, incomplete secondary moult and irregularities in the moult sequence (Stresemann & Stresemann 1971, Neufeldt 1981, Roselaar in Cramp & Perrins 1993). Three more Palearctic passerines, Locustella certhiola, Lanius tigrinus and Pericrocotus divaricatus, are reported as having two complete moults annually (Stresemann & Stresemann 1971, 1972b, 1976). However in L. tigrinus and P. divaricatus, complete moult of the secondaries during the postbreeding moult has not been documented. Thus, they cannot be classified with certainty and may in fact belong to group 8 (postbreeding moult arrested within secondaries, complete prebreeding moult), together with those Phylloscopus trochilus retaining some secondaries during the postbreeding moult. In Z,. certhiola, it is not known whether the postbreeding primary moult is completed or whether the inner primaries are usually retained (similar to L. fluviatilis}, and whether birds performing an (almost) complete postbreeding moult have a complete or partial prebreeding moult (Roselaar in Cramp 1992). Some individuals of species which normally carry out their complete moult in Africa have been found to moult completely in Europe (group 11 in Table 2; Sylvia borin see part II, caged Lanius collurio, Kramer 1950). However, it is not known whether or not these individuals also perform a second complete moult in the non-breeding area, and thus belong to group 7. In Locustella luscinioides, this seems improbable according to some authors (e.g. Glutz &: Bauer 1991, Roselaar in Cramp 1992) and, consequently, individuals moulting completely in the breeding area might belong to group 1, even though a second complete moult cannot be excluded.
3.3.5 Conclusions As shown in the above, a thorough description of the sequence of plumages acquired by successive moults - the basis of any comparative study on moult - has still not been completed, especially for European trans-saharan migrants. Sadly, this prevents our being able to give reliable plumage and moult cycles for trans-saharan migrants and leads to
Timing and duration of the complete moult the approximate moult strategies presented in Tables 1 and 2. We are well aware that the description of the moult patterns in trans-saharan migrants presented above and in Table 2 is sometimes based on scant or speculative information. More detailed studies, especially of the species mentioned in groups 11-14, will certainly add more species to the groups mentioned here, modify and clarify the classification and interpretation of the moult pattern of certain species, and perhaps reveal additional moult strategies. In this respect, Locustella luscinioides with its wide variety of recorded moult patterns might be a promising species for further studies (Steiner 1970, Stresemann & Stresemann 1970b, Mead & Watmough 1976, Thomas 1977, Miiller 1981, Trias etal. 1982, Aidley & Wilkinson 1987, Bensch etal. 1991, Nikolaus & Pearson 1991). Many unresolved questions have been raised in the preceding sections and the following questions, in particular, merit further study. In certain trans-saharan migrants, it is still unclear whether or not there is a partial moult of the adults before autumn migration and, if so, whether or not this constitutes the beginning of the partial (e.g. Acrocephalus palustris, Locustella fluviatilis) or complete (e.g. Acrocephalus schoenobaenus] moult in Africa. The moult in Africa requires further study in order to see whether it consists of one or two moults (e.g. the postbreeding moult) or the completion of the postbreeding moult and an (overlapping?) prebreeding moult (e.g. Acrocephalus schoenobaenus, A. a. arundinaceus). This question is of special interest in birds with a seasonally divided moult of the remiges, since many Sylvia communis, S. cantillans and S. nisoria present two generations of wing-coverts, apparently acquired during the winter (cf. also Svensson 1992). In this context, the fact that some trans-saharan migrants moult certain feathers three times a year (Motacilla flava and Anthus cervinus, Pearson &C Backhurst 1973, DJ. Pearson in lift.} is significant and may represent the discovery of an additional moult, apart from the postbreeding and prebreeding ones. In summary (Table 1 and 2), European passerines exhibit the whole range from one to two complete moults each year to almost all possible partitions of the moults between the two main moult periods. However, most species and most individuals of a species cluster around particular patterns, justifying a classification into moult strategies. Most European passerines renew the whole plumage during a continuous complete moult, while seasonally divided moult occurs only in a relatively few long-distance migrants. The main moult period for most European passerines is in late summer/autumn, though many longdistance migrants moult in winter in their tropical non-breeding areas. In northern latitudes, late winter/spring seems to be a rather unfavourable season for an extensive moult, probably because of the demands of territory defence and courtship, rather low food resources and the spring migration. No Palearctic passerine is known to perform a complete moult during spring, except when still in its tropical wintering area and with the exception of Carduelis spinoides which has an unusually late breeding season in August in the Himalayas and moults completely in May and June after spring migration (Whistler 1940). Based on intraspecific variation, transitions between the main moult strategies are recognizable along two axes (Table 1 and 2): on the diagonal a shift of the main moult from summer (strategy 1 and 2) to winter (strategy 3) or vice versa and on the lower horizontal axis an extending of the postbreeding moult to a second complete moult. A seasonal division of moult appears to occur in two. ways. The first is to suspend the complete postbreeding moult for autumn migration or within the non-breeding area, usually conserving the basic moult sequence (classical suspended moult, group 5 and lOa in Table 2). Intraspecifically, this occurs in some species which normally moult completely in winter, but already start before autumn migration (e.g. hirundines) as well as in Anthus campestris which may moult completely before the autumn migration. It might have evolved by extending the normal onset of body-feather moult before autumn migration to some
23
remiges (hirundines) or by postponing the completion of the postbreeding moult to winter (A. campestris). The primary moult of Sylvia communis and S. cantillans are exceptional in showing the whole range from a complete moult in the breeding area to a complete moult in winter (see p. 123). The second way of dividing moult seasonally seems not to be by a clear suspension, but rather through an incomplete moult before the autumn migration followed by an incomplete moult in winter, which are only more or less complementary to each other and show changes to the basic moult sequence (interlaced postbreeding and prebreeding moult). This type of seasonal division might have evolved from the replacement of secondaries in preparation for a possible retention during the next moult (e.g. Sylvia c. communis, S. curruca and Ficedula hypoleuca occurring in group 3 and 4 of Table 2) and appears to be the normal strategy in S. nisoria. Whether the seasonally reversed pattern (group 6) is a classical suspended or an interlaced moult is unknown. Thus, given our present state of knowledge, moult strategy 4 may actually comprise two quite different strategies, i.e. the classical suspended moult and the interlaced postbreeding and prebreeding moult. In Sylvia communis, both strategies have certainly been found (seep. 123). A trend towards two moults each year appears in species with a complete prebreeding moult which renew extensive parts of their plumage during a postbreeding moult. Intraspecifically, this probably occurs in Sylvia borin (occurring in groups 10, 9 and 11) and possibly in some of the species of groups 12 and 13. As shown by Phylloscopus trochilus and some shrikes (Stresemann & Stresemann 1971), it is the postbreeding moult which tends to be incomplete. The converse trend, a complete postbreeding moult and a tendency towards a complete prebreeding moult has not been developed very far (group 3).
3.4 Timing and duration of the complete moult 3.4.1 Timing and duration of the complete postbreeding moult in the breeding area Broadly, the postbreeding moult is fitted in between the end of the reproductive season and the beginning of autumn migration, autumnal territorial behaviour or the seasonal reduction in food availability. Consequently, the time available for the postbreeding moult varies considerably among species and individuals and may be very short. Four different means of fitting moult into a short period exist.
Reduction of moult duration This is achieved mainly by reducing the intervals between successive feather loss, resulting in an increased number of simultaneously growing feathers and, consequently, in a reduction of flight capability (Fig, 19 and 20). Rapidly moulting birds become reluctant to fly or even more or less flightless (e.g. Oenanthe oenanthe, Williamson 1957b; Luscinia luscinia, Berger 1967; Plectrophenax nivalis, Stresemann & Stresemann 1970a, Green & Summers 1975; L. svecica, Sylvia c. communis, Phylloscopus trochilus, Haukioja 1971; Calcarius lapponicus, Francis et al. 1991). Birds moulting very quickly also show an increased growth rate of the individual primaries. While primary growth rates of small passerines with moult durations of 50â&#x20AC;&#x201D;90 days range from 2.1 to less than 3.4 mm per day (Zeidler 1966, Newton 1967, 1969, Dhondt 1973, Ojanen & Orell 1982, Winkler & Winkler 1985), the mean daily growth rates in the two fastest moulting birds (27â&#x20AC;&#x201D;37 days) are 4.2 and 5 mm per day (Luscinia luscinia, Berger 1967; Plectrophenax nivalis, Stresemann & Stresemann 1970a).
24
The Moult of Adults
Fig. 19. Serinus citrinella ad 6 in complete postbr moult, 23 August. P 1-4 full-grown, 5-6 growing, 7-10 old. S 1 growing, 2-6 old. T 7+9 growing, 8 full-grown. CC and GC 1-6+8-9 full-grown, 7+10 growing. Al and MeC old. MaC growing or full-grown, undermost row old. Example of a slow moulting short-distance migrant with two simultaneously growing primaries and almost fully renewed greater coverts, the median coverts being still old (c£ Fig. 20).
In these cases, moult regularly overlaps with feeding the young or even with incubation. In large species, such as the Corvidae, which generally have long moult durations, overlap between breeding and moult is also frequent (Gwinner 1966, Kalchreuter 1969, Dorka 1971, Holyoak 1974, Seel 1976, Winkler etai 1988). There are, however, small species with long moult periods, in which moult also overlaps with feeding, incubation or laying (e.g. Ptyonoprogne rupestris, Stresemann & Stresemann 1966; Sylvia melanocephala, Cisticola juncidis, Gauci & Sultana 1979, 1981; Parus major, P. caeruleus> Flegg & Cox 1969, Dhondt 1973; P. montanus, Orell & Ojanen 1980; Sitta europaea, Matthysen 1986; Passer domesticus* Alonso 1984). In these species, the maintenance of flight capacity (especially in Ptyonoprogne rupestris) or the reduction of energy and nutrient demands during moult is apparently paramount. Generally, overlap between breeding and moult is more common in S than in ? and usually connected with a reduction or abandonment of parental care. During breeding, usually only one or a few innermost primaries are moulted, and rarely some tertials, rectrices and secondaries (Orell & Ojanen 1980). Moult progresses considerably more slowly than normally (van Hecke 1980, Boddy 1983) and, in Pyrrhula pyrrhula, does not include the body-feathers (Newton 1966). As shown by P. pyrrhula, Phylloscopus trochilus and Passer montanus^ it may be so slow that the next primary is only shed after the preceding one is full-grown, thus giving the impression of a suspended moult (Newton 1966, Kasparek 1979b, van Hecke 1980, Norman 1990b, Fig. 21). Primary moult may also start during or soon after breeding, but be suspended if another breeding attempt is made (van Laeken & Caekebeke 1982, Boddy 1983, 1992, Harper 1984).
Overlap between moult and autumnal activities Intense moult during migration does not occur in European passerines and was never observed among the many migrants we caught on Col de Bretolet. However, migration during the final stages of moult (P 9 or S 5 and 6 are still growing) occurs regularly (see part II, Evans 1966, Haukioja 1971, Hyytia & Vikberg 1973) and moult during the beginning of the autumn migration has been suggested for Motacilla flava
Fig. 20. Sylvia curruca ad in complete postbr moult, 25 August. P 1 fullgrown, 2—6 growing, 7—10 old. S 1 growing, 2—6 old. T 7+9 growing, 8 fullgrown. Al old. CC full-grown. GC all growing. MeC all growing. MaC old, growing or full-grown. Example of a fast moulting long-distance migrant with five growing primaries and simultaneously growing greater and median coverts (cf.Fig. 19)
Overlap between breeding and moult In species whose moult extends over a medium or long period, moult usually starts as soon as the young of the last brood become independent. However, late breeders may commence moult earlier; while caring for fledged young or even feeding nestlings (e.g. Carduelis flammea^ Evans 1966; Pyrrhula pyrrhula > Newton 1966). Overlap between breeding and moult is a regular phenomenon in species with short moult periods, such as long-distance migrants and birds breeding in the far north (e.g. Anthus trivialis, Luscinia megarhynchos, Phoenicurus phoenicurus^ Turdus iliacus, Sylvia curruca, Ficedula hypoleuca> Phylloscopus trochilus, Carduelis flammea, Pinicola enucleator, Calcarius lapponicus, Plectrophenax nivalis; Creutz 1955, Haukioja 1971, Haukioja & Kalinainen 1972, Hussell 1972, Green & Summers 1975, van Hecke 1980, Tiainen 1981, Ojanen & Orell 1982, Boddy 1983, Ginn & Melville 1983, Rvmkcvich 1990, Underbill etaL 1992),
Fig. 21. Anthus trivialis ad 9, with broodpatch, in suspension of recently started postbr moult, 10 August. P 1-2 are full-grown, P 3-10 still old. There are no feathers growing either on the body or wings. This bird is probably still breeding or caring for fledged young and has either temporarily stopped its postbr moult or is moulting very slowly.
Timing and duration of the complete moult
(Hereward 1979, Dittberner & Dittberner 1987). Ptyonoprogne rupestris apparently moults slowly during the autumn migration (Elkins & Etheridge 1977). In Phylloscopus trochilus and perhaps in many other long-distance migrants, moult seems to be timed so as to finish before the endogenously programmed start of migration, thus often overlapping with breeding (Tiainen 1981, Bensch et al. 1985, Underfill! rf*/. 1992). It also seems that moult is reduced in intensity, or avoided entirely, while defending territories in the autumn (Parus major, Dhondt 1973, 1981; Sitta europaea, Matthysen 1986; Passer montanus, Myrcha & Pinowski 1970) and while storing food for the winter (Parus montanus, Orell & Ojanen 1980). Dhondt (1973) suggests that <S Parus major in Belgium slow down their moult as an adaptation to the overlapping of moult and autumnal territorial behaviour by starting earlier (often during second broods) and finishing slightly later than the 2. Similarly, Gauci & Sultana (1981) argue that the moult of c? Cisticola juncidis is considerably longer than that of $ (92 versus 67 days) to allow for territorial defence against early-hatched first-year cJ, which are ready to breed even at this early age.
Arrested moult Some individuals do not complete their postbreeding moult, but retain some unmoulted feathers. This may happen 'accidentally' in almost every species, but seems to be more frequent in birds with short moult periods (long-distance migrants, northern populations, late breeders) and in Carduelis spinus whose breeding season is very prolonged. In most species which arrest the flight feather moult, the feathers to be moulted last (S 6, S 5—6, alula) are those retained (Sturnus vulgaris see section 3.2.3). In those species with one moult annually, these retained feathers are probably not moulted until the next complete postbreeding moult. In species which perform an extensive prebreeding moult, the retained feathers are usually moulted in the winter (see section 3.3.3 and 3.3.4).
Moult duration The timing and duration of the complete postbreeding moult in the breeding area has been studied in a large number of species and populations, usually with reference to the primary moult • (summarized in Ginn & Melville 1983). The start, duration and end of the moult, as well as the time needed for growth of the individual feathers, can be estimated from a sample of free-living birds caught only once, from recaptures, from captive birds or by counting the daily growth bars of shed feathers (Green 1974, Winkler et al 1988). Considerable statistical problems are involved when estimating the timing and duration of moult from birds caught only once (discussed by e.g. Evans 1966, Newton 1966, 1967, Pimm 1976, Kasparek 1980, Summers et aL 1983, Winkler et aL 1988) and the best analysis currently available (Underhill & Zucchini 1988, Underfill! et al. 1990) has not yet been used widely. Hence, many published estimations of moult duration are likely to be biased and not comparable. Nevertheless, the following generalizations can be made regarding the mean durations of primary moult (data from Ginn & Melville 1983, supplemented by more recent publications). In European passerines, the duration of primary moult depends only roughly on the size of the feathers. Large birds generally have longer primary moult durations than small birds (e.g Corvus corax 140-145 days, C. corone and C, frugilegus 105-172 days, smaller Corvidae 92-182 days). Thrush-sized birds have only slightly longer moult durations than smaller passerines (large thrushes and Sturnus vulgaris 70—100 days; Turdus torquatus alpestris, T. philomelos and T. iliacus
25
50—60 days) and relatively short durations in N Scandinavia (T. iliacus at 70° N 40 days, T. pilaris 51 days). Resident populations of small passerines generally take 60-85 days for primary moult, exceptions being Prunella modularis in Great Britain with only 54—60 days (Ginn 1975), Panurus biarmicus with only 45-55 days (Ginn & Melville 1983) and Cisticola juncidis in Malta with 67-92 days (Gauci & Sultana 1981). In partial migrants, primary moult lasts between 50 and 85 days and in short-distance migrants 45—60 days, exceptions being Motadlla altavndi 68-73 days (Ginn & Melville 1983) and Carduelis flavirostris with 75 days (Ginn & Melville 1983). Long-distance migrants (30-50 days) and the two arctic breeders Calcarius lapponicus and Plectrophenax nivalis (28—40 days) have the shortest primary moult durations yet recorded for European passerines.
Timing of moult In birds which moult over a medium or long period, there is considerable variation in the onset and duration of moult between individuals within a population, between years and between populations. In these species, birds breeding late (late breeders, years with a late breeding season, northern populations) usually start moult later than early breeders, but normally moult faster and may compensate almost totally for any seasonal delay (e.g. Parus major, P. caeruleus, Flegg & Cox 1969; Passer domesticus, Zeidler 1966, Haukioja & Reponen 1968; P. montanus, Deckert 1962; Fringilla coetebs, Dolnik & Blyumental 1967, Dolnik & Gavrilov 1980; Carduelis flammea, Boddy 1983; Pyrrhula pyrrhula^ Newton 1966; Emberiza schoeniclus, Kasparek 1980; Sturnus vulgarity Meijer 1991). For example, in Finland moult is shortened in Parus major by 8 days, in Phylloscopus collybita by 10 days and in Motadlla alba by 20 days compared to Great Britain or central Europe (Orell & Ojanen 1980, Ginn & Melville 1983), However, the onset of moult may be earlier and moult duration longer in northern than in southern populations if northern populations have only one instead of two broods annually (Emberiza schoeniclus, Kasparek 1980). In birds with short moult periods (long-distance migrants), moult is more synchronized within populations and moult duration hardly differs between southern and northern populations, moult having apparently already been shortened as much as possible (Phylloscopus trochiluS) Motadlla flava^ Phoenicurus phoenicurus, Saxicola rubetra^ Sylvia c. communis\ Ginn & Melville 1983, Underhill etaL 1992). In the majority of species studied, <J commence moult earlier than $, and reduce their share of parental care if they still have dependent young. 9 then have shorter moult durations in order to catch up (e.g. Orell & Ojanen 1980, Francis etaL 1991). In some species, no difference in timing between the sexes was observed (Sylvia melanvcephala^ Gauci & Sultana 1979; Passer hispaniolensis, Alonso 1984; Carduelis flammea in Great Britain, Evans 1966; Sitta europaeay Matthysen 1986; Motadlla flava, Hereward 1979; Fringilla montifringilla^ Ottosson & Haas 1991). Non-breeders (often second-year birds) and failed breeders usually start moult earlier than successful breeders (e.g. Corvidae, Bahrmann 1958, Kalchreuter 1969, Dorka 1971, Holyoak 1974, Seel 1976, Winkler etaL 1988; Pyrrhulapyrrhula, Newton 1966; Sitta europaea> Matthysen 1986; Cinclus cinclus, Richter 1954). The timing and duration of the complete postbreeding moult are therefore intimately related to both the preceding breeding season and the oncoming autumnal activities (e.g. migration, territorial behaviour, food storage etc.). Thus, trade-offs between flight capacity, energy and nutrient demands (moult duration), the length of the breeding season and period of parental care (overlap between moult and breeding) can be expected to operate. Until now, very few studies have investigated the effects of moult on other events in the life of birds in detail. For instance, Dhondt (1973, 1981) suggests that S Parus major may either start the postbreeding moult during the first brood and finish it before the autumnal territorial contests begin, or raise a second brood before
26
The Moult of Adults
moulting more slowly during autumnal territorial behaviour, in which case possibly shorter wings are grown. Bensch etal (1985) found that 5 Phylloscopus trochilus with small broods begin their moult just after hatching while ? with large broods start moult only once the young reach independence. The possible disadvantages faced by 9 with large broods who moult late might be to retain some secondaries or to moult at a faster rate. Thus, there may be a trade-off between clutch size and moult.
3.4.2 Timing of moult in tram-saharan migrants Various explanations have been proposed to account for the timing of moult in trans-saharan migrants. Pearson (1973) noticed that longdistance migrants which reach equatorial or southern latitudes frequently moult completely in Africa (see also Ginn & Melville 1983). He suggested that more time is available for the moult in Africa than between the breeding season and autumn migration and that the rapid and demanding spring migration can be undertaken with the benefit of new feathers. Swann & Baillie (1979) also pointed out that since the breeding season in E Europe is delayed, the time period available for a premigratory moult in eastern breeding populations is even shorter (e.g. in Sylvia communis icterops). Bensch etal. (1991) suggest that a tropical climate may also be helpful in reducing heat loss during feather replacement, though Aidley & Wilkinson (1987) argue that low temperatures are the reason for moult suspension in Acrocephalus schoenobaenus in Nigeria. Alerstam & Hogsted (1982) proposed that species whose nonbreeding area is larger than the breeding area may be expected to moult under the more relaxed conditions of the non-breeding area. The large variation in moult patterns suggests that the timing and duration of moult in any particular trans-saharan migrant is actually determined by the interaction of several factors, such as the timing of the end of the breeding season (which varies geographically and between individuals, e.g. failed breeders, those with second broods), the timing of autumn migration, the degree of flight capability to be maintained during moult, the seasonality and predictability of the environment as well as the inter- and intraspecific competition in both the breeding and the non-breeding area. The outcome of these highly complex trade-offs varies considerably between and within species, populations and individuals, as well as between years (e.g. Hyytia & Vikberg 1973, Berthold & Querner 1982a). Although our knowledge of the ecology of trans-saharan migrants is still limited, some broad trends can be proposed. In the northern tropics, migrants arrive at the end of the summer rains to find a rich abundance of insect life which, however, soon starts to decline (Aidley & Wilkinson 1987, Bensch et al. 1991). Thus, migrants wintering in subsaharan Africa, north of about 10° N, are faced with a short period favourable for moulting. Migrants wintering entirely in this area should either moult in the breeding area or try to arrive in the wintering area as soon as possible and moult there rapidly, or else split their moult into a first part in the breeding area and a second in the wintering area. Indeed, Fig. 22 shows that in the N African steppe and savanna belt (north of about 10° N in the west, extending further south in E Africa) over 70% of wintering European passerine species moult in the breeding area. The minority which perform a complete moult in this summer rainfall area moult before the end of November and as rapidly as do some long-distance migrants in N Europe (Aidley & Wilkinson 1987, Bensch etal 1991, Hedenstrom et al. 1993). Moreover, all those migrants which regularly divide their moult seasonally winter in the steppes and savannas of N and NE Africa (Anthus campestris, Locustella lu$cinioides> Sylvia communis communis and some Sylvia c. icterops, S. nisoria, S. hortensis, S. cantillans, Lanius nubicus, L. senator niloticus, Emberiza hortulana, E. caesia). Thus, a seasonally divided moult of the remiges might serve to fit moult into the two short moult periods before and after autumn migration. However, as shown by Locustella luscinioides and first winter
Fig. 22. Percentage of the total number of European passerine species present which perform a complete moult in their wintering grounds in the various parts of trans-saharan Africa. Species and their wintering distributions are taken from Moreau (1972).
Lanius senator in N Ghana, species moulting only part of the remiges may maintain a higher degree of flight capability by moulting more slowly (Bensch etal. 1991). Birds which winter around the equator and further south do not experience a prolonged drought during their stay (Moreau 1972, Pearson & Lack 1992), and hence generally encounter a prolonged favourable period for moulting. Fig. 22 shows that the proportion of European passerine species undergoing a complete moult in the wintering area increases markedly towards the southwest. Moult duration there is generally longer than in Europe or N Ghana (summarized in Ginn & Melville 1983, Dowsett-Lemaire & Dowsett 1987, Bensch et al 1991). A direct intraspecific comparison of moult duration is provided by Phylloscopus trochilus which takes 37 days to perform a complete moult in the breeding area, but 50â&#x20AC;&#x201D;68 days in southern and central Africa (Underhill etaL 1992). The pattern of the rainy seasons in Africa profoundly influences the seasonal distribution, migratory patterns and moult periods of European migrants (Pearson 1990, Pearson & Lack 1992). The moulting season in E Africa generally coincides with the wet season and gets progressively later towards the south (Pearson 1973, Hanmer 1979). Many migrants follow the rains as they move south during the autumn and winter and regularly have two moult periods, one in autumn somewhere in NE Africa and a second after about December in the southern part of Africa. Thus, they may either divide their complete moult into two temporally separate phases (e.g. group lOa in Table 2) or may perform an additional partial moult either in NE Africa (e.g. Locustella fluviatilis, Acrocephalus palustris which moult completely in southern Africa) or in southern Africa (e.g. those Acrocephalus schoenobaenus moulting completely in NE Africa, see section 3.3.2). E and W Africa, therefore, provide different conditions for moult. In E Africa, migrants can successively exploit areas both
Timing and duration of the complete moult
north and south of the equator over a large Nâ&#x20AC;&#x201D;S range, all of which provide a wide variety of habitats, especially savannas which are favoured by many migrant species. In W Africa, they are squeezed into the narrow strip north of the equator between the Sahara and the rain forest, from which they have little access to areas with late winter rains. A situation similar to that in E Africa is found on the Indian subcontinent where several Palearctic migrants (e.g. Acrocephalus dumetorum, A. agricola, Sylvia hortensis, Hippolais caligata) apparently exploit the temporarily abundant food resources in N India after the summer rains for a complete moult and then migrate further south in early winter when this area dries out (Gaston 1976). Similarly, Emberiza a. aureola. moults completely in E China during autumn, before migrating to SE Asia with a fresh plumage (Stresemann & Stresemann 1969a). The timing of the breeding season also affects the timing of moult in trans-saharan migrants. Sylvia c. icterops breeds later than S, c. communis (Swann &: Baillie 1979) and, in addition, encounters no drought period in its southern African wintering grounds. Both the time constraint in its breeding area and the conditions in its wintering area favour its moulting predominantly in Africa. The converse is true of Lanius senator. L. s. senator, wintering in W Africa, breeds about one month later than L s. niloticus of the Near East which winters in NE Africa. While the nominate subspecies moults the remiges in the wintering area, niloticus moults the primaries in the breeding area, but retains some or all of the secondaries (Nikolaus & Pearson 1991). There are, of course, exceptions and special cases to the very general pattern outlined above: some species (Sylvia cantillans, Hippolais pallida, Phylloscopus bonelli> Lanius senator senator) moult in the Sahel area and appear to be well adapted to dry habitats. 5. cantillans continues moulting even when Acrocephalus schoenobaenus suspends moult (Aidley & Wilkinson 1987). Other species performing a complete moult in the northern tropics include warblers of the genera Acrocephalus and Locustella which breed very late in the season and might be forced to moult in Africa by time constraints in the breeding area. Furthermore, their usual wetland and seasonally flooded habitats tend to persist some time into the dry-season, even in Africa. Ficedula
27
hypoleuca, F. albicollis, Luscinia megarhynchos and L. luscinia winter mainly south of 10° N, but perform a complete moult in the breeding area. It would be interesting to compare the ecological conditions for these species during the non-breeding season in the breeding and nonbreeding area. The hirundines need adequate powers of flight during their entire life, and must moult slowly over the entire non-breeding season starting with moult of the body-feathers, and rarely the innermost primaries, in the breeding area. Their moult takes longer than any of the other small European passerines (121â&#x20AC;&#x201D;185 days; see part II and Ginn& Melville 1983). In summary, the timing of moult of trans-saharan migrants is still poorly understood, despite the general trends summarized above. In particular, it is still unclear as to why there are so many different seasonally divided moult strategies. Although most species cluster into distinct moult categories, moult cycles can be highly variable within a species and apparently adapted to the ecological conditions specific to a population or individual. Thus, the moult and plumage cycles of trans-saharan migrants cannot be considered as inflexible regimes, but rather as highly adaptive processes, sensitive to immediate environmental influences. Precisely how environmental conditions influence prebreeding and seasonally divided moults has hardly been studied. Berthold & Querner (1982a) concluded that the seasonal division of moult of Sylvia hortensis is not endogenously controlled, but is influenced in some way by the preceding breeding season (but probably not simply controlled by the end of breeding). T. Fransson (in lift.) found that one individual Sylvia c. communis retained one, four and five secondaries after three consecutive postbreeding moults. Studies on the control of moult in trans-saharan migrants while in Africa are few. They seem to utilize favourable environmental conditions during late summer in Europe, during autumn in the northern tropics and during winter in equatorial and southern latitudes (D. J. Pearson in lift.) where they may perform one to three partial and/or one or two complete moults which may be suspended during autumn migration or within Africa. How these, apparently individually variable, moult strategies are controlled and how, if ever, they can be related to moult cycles invites further exploration.
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CHAPTER 4
The Moult During the First Year of Life 4.1 Introduction to the moult cycles At fledging, all young passerines wear the juvenile plumage, which differs from that of adults in two respects: first, it consists of fewer feathers and these are more loosely textured; second, in many species, its coloration differs. When the juvenile plumage is fully grown, it is fresh, while that of the adults is usually worn and in need of replacement. Consequently, the plumage cycle of juveniles is out of phase with that of the adults and must be brought into line with the adult cycle without replacing feathers too often or keeping them too long. In addition, environmental factors bind the juveniles to the same two general moult periods, in late summer/autumn and winter, as the adults. The moults during the first year of life must, therefore, address these issues and bring the juvenile plumage into the adult form. Depending on the moult strategy of the adults and the relative nature of the juvenile and adult plumages, the various European passerines display a range of moult cycles, which are summarized in Table 3. Note that the cycles numbered 1-15 are a product of the juvenile moult pattern and the various adult moult strategies described in section 3.3Most species whose adults perform a complete postbreeding moult in the breeding area change the juvenile body-feathers from some weeks to a few months after fledging. The juvenile remiges are retained slightly more than a year, until the next postbreeding moult when young birds enter the adult moult cycle (moult cycles 5 and 6). The postjuvenile moult is of variable extent and may include some primaries and secondaries (moult cycles 3 and 4). Only a few species renew the entire juvenile plumage soon after fledging with a complete postjuvenile moult (moult cycles 1 and 2). In species with a partial prebreeding moult, first-year birds also perform this moult, thus replacing the postjuvenile body-feathers within a few months of their first growing them (moult cycles 2, 4 and 6). In species whose adults perform a complete moult in a tropical wintering area, the partial postjuvenile moult is either of limited extent or virtually absent and the first-year birds usually rapidly align their moult with the adult pattern by also performing a complete moult in the non-breeding area (moult cycles 9 and 15). In species whose adults may show a seasonally divided moult of the remiges, the first-year birds perform a postjuvenile moult of limited extent and may also renew part of the remiges during an extensive first prebreeding moult (moult cycles 7, 8 and 12). Exceptions to the above and more complex moult cycles (moult cycles 10, 11, 13 and 14) are treated in section 4.6. In summary, most juvenile body-feathers are replaced soon after fledging, or at most after about six months in some long-distance migrants. The juvenile remiges, however, are usually-kept either for about a year, or for about six months in certain long-distance migrants. Less frequently, they may be shed after only a few weeks or months in species which perform a complete postjuvenile moult, or be retained for more than a year in species which migrate to tropical Asia (see section 4.6.2) and possibly also in some species which exhibit a seasonally divided moult of the remiges (see section 4.6.4). The juvenile wing-coverts, tertials and rectrices may be moulted together with the body-feathers or else with the remiges.
4,2 The juvenile plumage 4.2.1 Completion of the juvenile plumage after fledging At fledging, the first set of juvenile body-feathers is usually full-grown or almost so, but the remiges, rectrices and underwing-coverts are still growing and large parts of the body remain bare. An additional set of juvenile body-feathers grows after fledging in most passerine species (Rymkevich 1990, Dorsch 1993), and this has been described in detail for four species of Phylloscopus warblers (Gwinner 1969), Sylvia borin, S. atricapilla (Berthold et aL 1970) and Acrocephalus melanopogon (Leisler 1972). In some long-distance migrants, this second set is already growing during the last days in the nest. These feathers grow predominantly at the edges of the existing feather tracts and cover any extensive bare parts, especially on the breast and belly, but they also grow within the feather tracts of the nape, head and undertail-coverts. This completion of the juvenile plumage should not be confused with the postjuvenile moult which usually starts in the centre of the body-feather tracts. The growth of the second set of juvenile bodyfeathers and the postjuvenile moult overlap in long-distance migrants, but are separated by about three weeks in Phylloscopus coliybita (Fig. 23; Gwinner 1969, Gwinner et ai. 1971) and probably by more than a month in Parus caendeus (Bensch & Lindstrom 1992). Species with an accelerated juvenile development (Sylvia borin, Phylloscopus trochilus, P. bonelli, P. sibilatrix) do not renew the second set of juvenile feathers during the postjuvenile moult. Species with a slower postjuvenile development (short-distance migrants and residents) do so while growing a third set of additional body-feathers (S. atricapilla, P. coliybita and Acrocephalus melanopogorr, Gwinner 1969, Berthold et aL 1970, Gwinner etal. 1971, Leisler 1972, Dorsch 1993). However, latehatched short-distance migrants and residents may retain the second set (Rymkevich 1990).
4.2.2 Structure of the juvenile plumage In most species, the juvenile body-feathers are more loose in texture than those of adults, especially on the nape and undertail-coverts (Fig. 24). Compared with the adult body-feathers, there are fewer, more widely spaced, barbs and fewer barbules with booklets interlocking adjacent barbs (Gohringer 1951). Only a small area at the tip of the juvenile body-feathers is firmly interlocked. Thus, the individual juvenile feathers are lighter in weight and the total mass of the bodyplumage less than in adults. As shown for Sylvia atricapilla, the total number of body-feathers may also be smaller (Berthold & Berthold 1971). In a few species, the juvenile body-feathers are of relatively firmer texture than those of most other species (e.g. Locustella naevia, Acrocephalusschoenobaenus, Roselaar in Cramp 1992; hirundines). Whether the juvenile remiges of European passerines are also more loosely textured than those of the adults has not been studied, but inspection by eye, at least, does not show conspicuous differences (in contrast to tropical species, Fogden 1972). However, the juvenile flight feathers, especially the rectrices, are often narrower and more pointed
30
The Moult During the First Year of Life
Table 3. Moult cycles during the first one and a half years of life in European passerines. Moults indicated in bold are different in extent from those shown by adults at the same season. Moults in parenthesis occur in some individuals only. Partial moult denotes a moult without renewal of the secondaries and primaries. The extent of the various moults are simplified (see text for details). Moult cycle 9 may consist of various cycles (see text and section 3.3.2). For reference, the moult strategy of the adults is indicated (see Tables 1 and 2). Some individuals may switch from one moult cycle to the other (not indicated). Other moult cycles of transsaharan migrants (see section 4.6) and moult cycles ofLoxia curvirostra (see p. 182) and Cisticolajuncidis (see section 4.4.4) are not included. Moult cvcle
First summer/ autumn
First winter/ spring
Second summer/ autumn
Second winter/ spring
Postjuvenile rnoult
First preb reeding moult
First postbreeding moult
Second prebreeding moult
1
complete
—
—^- complete
2
complete
——^- partial
—^~ complete
3
partial + P
—
—^ complete
4
partial + P
—
5
partial
—
6
partial
—
7
partial
——^- partial + S
—^- complete, except S — —^- partial + S
8
partial
——^- partial + P eccentric
—>• P suspended
9
(partial)
——^- (partial) complete (partial) —^- (partial)
^- partial
—^- complete
—^- partial
—>- partial
—^- complete ^~ partial
—^- complete
Examples
*- e.g. Passer domesticus species see p. 53
1
^- Acrocephalus melanopogon
2
*- e.g. Carduelis chloris species see p. 55
1
*- e.g. Sylvia meianocephala species see p. 59
2
^ —>- partial
Moult strategy of adults
e.g. Erithacus rubecula species see p. 55
>• e.g. Motacillaflava species see p. 59 ^ e.g. Sylvia nisoria species see p. 59
1 2 4 group 3+4 4 group 5
—^- resumption + partial
^- e.g. Sylvia communis species see p. 59
—^- (partial) complete (partial)
^~ e.g. Acrocephalus scirpaceus species see p. 59
3
10
—>> partial (+ P eccentric)
—>- complete
^- Carpodacus erythrinus
3
11
—^- partial
—^ complete —^- partial
^- Emberiza a. aureola
3
—^- complete except S
^> e.g. Oriolus oriolus
4 group 6 3
^- partial
12
partial
——^ complete except S
—^- partial + S
13
partial
——>- partial + P eccentric
—^- partial + P suspended
14
partial
——*-
—^- partial
—^- partial + P —*~ complete
^ Locustella fluviatilis
5
15
partial
——^- complete
—^ complete
—^- complete
^* Phylloscopus trochilus
6
^ complete
•*- resumption
^> Lanius senator
Fig. 23. The progress of juvenile plumage development and the postjuvenile moult in four species of Phylloscopus warbler, showing the differences between the species. t^sSS^I the main period during which the second set of juvenile feathers develops. These feathers develop as shown: '(//////A on the back, upper belly, crown and nape, I>0\\\\NI on the chin and cheek, I I on the belly and flanks. ^BH shows the period during which the postjuvenile moult occurs. (After Gwinner 1969).
Fig. 24. Phylloscopus collybita in juvenile plumage (left), 5 August, and after postjuvenile moult (right), 19 September. The body-feathers of the juvenile plumage are more loosely textured than those of the first non-breeding plumage and all subsequent plumages.
than those of the adults. They are also slightly shorter on average, with the exception of the juvenile outermost primary which in many species is longer than in adults (this is very conspicuous in Panurus biarmicus). Thus the wings of juveniles are often slightly more rounded than those of the adults (Alatalo etal. 1984, Winkler & Winkler 1985). There appear to be two possible explanations for the loosely textured body-feathers of juveniles which are difficult to distinguish from each other. First, if the different colour of the juvenile plumage is required for only a short time and needs to be changed soon in order to fulfil
other behavioural functions (see section 4.2.3), there might be no need to develop a durable juvenile plumage. Second, nestlings which grow a loose juvenile plumage may spend less energy in feather growth and may thus fledge earlier or have more energy to direct into other body structures than nestlings which form a durable plumage (see also Fogden 1972). This would also prompt replacement of the imperfect juvenile feathers soon after fledging. This second hypothesis is supported by the fact that species with a juvenile plumage similar in colour to that of the adults also have a loosely textured juvenile
The juvenile plumage
31
plumage and that most passerines complete the juvenile plumage after fledging by adding a second set of juvenile feathers.
4.2.3 Coloration of the juvenile plumage In most European passerines, the juvenile plumage is cryptic and inconspicuously coloured. In many species, it differs markedly from that of the adults, but usually only on those feathers which are moulted soon after fledging such as the body-feat hers, wing-coverts and in a few species also the tertials and rectrices. The remiges are generally the same colour as in the adults. The juvenile body-plumage generally lacks conspicuous coloration (e.g. Erithacus rubecula, Regulus spp., Carduelis carduelis, Pyrrhula pyrrhula; Fig. 25 and 26). It is often spotted, streaked or barred (e.g. Turdidae, Muscicapidae, Laniidae, Prunella modularisy Cinclus cinclus), without gloss (e.g. Sturnus vulgaris, S. unicolor)y less intensely coloured (e.g. Motacilla spp., Parus major, P. caeruleus), and in sexually dimorphic species is more like the adult $ than the adult 6 plumage (e.g. Monticola saxatilis, Turdus merula, Sylvia atricapilla, Panurus biarmicuSy Passer domesticus, Fringilla coelebs^ Carduelis cannabina, C. flammea, Emberiza schoenidus). An exception is Tichodroma muraria whose juvenile wing-coverts are conspicuously coloured like the postbreeding plumage of the adults. The juvenile body-plumage is similar in coloration to that of the adults only in species in which the adult plumage is also inconspicuous and cryptic (e.g. Sylvia borin and most warblers of the genera Acrocephalus, Phylloscopus and Hippolais). The feathers acquired at the postjuvenile moult are generally adultlike in colour, although they may be less bright or have broader fringes (e.g. the head-feathers in Sylvia atricapilla and Fringilla montifringilla). Exceptions are some cJ Phoenicums ochruros, Carpodacus erythrinus and Oriolus oriolus which take on a 9 -like plumage in their first year, Lanius collurio and L. nubicus in which the postjuvenile feathers differ considerably from those of the adults and form a second juvenile plumage (see p. 154) and Sylvia nisoria in which the postjuvenile body-feathers and wing-coverts differ slightly but consistently from those of adults. The juvenile secondaries and primaries, which are kept for longer, are always the same colour as the adults with the exception of very few
Fig. 25. Regulus regulus in juvenile plumage (left), 7 August, and after postjuvenile moult (c?, right), 5 September. The juvenile body-feathers of many passerines lack conspicuous coloration, as for example the black and yellow crown in this Goldcrest. After the postjuvenile moult, the body-feathers are generally coloured as in the adult and express any sexually dimorphic characters, as for example the orange centre of the crown in this S Goldcrest.
Fig. 26. Carduelis carduelis in juvenile plumage (left), 24 August, and after postjuvenile moult (cÂŁ, right), 31 October. The juvenile plumage lacks the conspicuous colour pattern of the head. During the postjuvenile moult, the adult colour pattern is acquired.
Fig. 27. Tichodroma muraria after postjuvenile moult, 14 September. In most passerines, the juvenile remiges already show the colour pattern of the adults. species (e.g. Bombycillagarrulus). Conspicuous patterns on the remiges, for instance the yellow marks on the remiges of Carduelis carduelis (see p. 172) or the red on the remiges of Tichodroma muraria (Fig. 27), are already fully developed in juveniles. The sex of juveniles can therefore be determined in species with sexually dimorphic remiges (e.g. Turdus merula, Coccothraustes coccothraustes, Carduelis cannabina, C. Moris}. Two adaptive advantages have been attributed to the particular coloration of the juvenile plumage. First, the general cryptic effect of the juvenile plumage can be related to their lack of experience and consequently a greater vulnerability to predators. Second, the lack of conspicuous and distinctive patterns on the juvenile plumage may serve in intraspecific signalling. Many juveniles fledge while the adults are still territorial and producing second or substitute broods. A distinct juvenile plumage signals their status and avoids either aggressive or amorous responses from adults during the difficult first phase of independence. Lack (1943) showed that stuffed Erithacus rubecula in juvenile plumage are hardly attacked by adults during the breeding season while those in adult plumage are. However, we know of no behavioural studies investigating the effect of the juvenile plumage during the postbreeding season of European passerines.
4.3 Sequence of postjuvenile moult Complete postjuvenile moult The complete postjuvenile moult generally follows the basic sequence described in the discussion of the complete adult moult (section 3.2). No differences have been reported between the sequence of the complete postjuvenile moult and the postbreeding moult of conspecific adults (e.g. Zeidler 1966, Spitzer 1972, Pearson 1975b, Alonso 1984, Peris 1988). However, in Sylvia melanocephala, the renewal of the secondaries and tertials in juveniles starts later relative to the progress of the primary moult than in adults (Gauci & Sultana 1979).
Partial postjuvenile moult The partial postjuvenile moult starts on the upper- and underparts and soon includes the marginal coverts and feathers of the head. The under-
32
The Moult During the First Year of Life
and uppertail-coverts, as well as the median covens, are shed next, followed by the greater coverts and later by the alula, tertials and rectrices. The first areas to complete the moult are the marginal and median coverts, the tail-coverts and parts of the body. The head feathers are usually the last to be moulted. The tertials and rectrices are often not full-grown until much later than the greater coverts, so that in many species the final extent of the postjuvenile moult can only be determined when all the feathers on the wing are full-grown. The sequence of the postjuvenile moult of the body-feathers varies somewhat between species, and detailed descriptions are available for only a limited number (e.g. Sylvia borin and S. atricapilla^ Berthold et aL 1970; Sylvia spp. and Phylloscopus spp. Norman 1981, 1990a, 1991a, Bensch & Lindstrom 1992; Anthus spinoletta, Prunella modularis, Turdus torquatus alpestrisy Winkler & Jenni in Glutz & Bauer 1985, 1988; Pyrrhula pyrrhula, Newton 1966). In species and individuals with a protracted moult duration, the different feather tracts enter the postjuvenile moult successively and fewer feathers grow simultaneously than in species and individuals whose moult duration is short. In the latter, many feather tracts commence moult simultaneously (e.g. Dolnik &: Blyumental 1967, Berthold etal. 1970) and individuals may have well over half of the body-feathers growing simultaneously (e.g. a regular feature in Sylvia curruca). The progress of the formation of the second set of juvenile feathers and of the postjuvenile moult can be used to estimate the age (in days) of juveniles up to the end of the moult (e.g. Bensch & Lindstrom 1992), provided that differences in the onset, speed and sequence of moult between early- and late-hatched birds are taken into account (see sections 4.4.1 and 4.4.3).
4.3.1 Sequence within wing-feather tracts during partial postjuvenile moult
by T 9 and later by T 7 (divergent sequence; Parus caeruleus, Flegg & Cox 1969; Phylloscopus collybita, Norman 199la; Motacilla cinerea*, Herremans 1988a). This divergent sequence is also suggested by the frequency distributions of renewed tertials in about half of the species examined (Fig. 28). However, considerable individual variation exists and T 7 or T 9 may occasionally be renewed alone. In the remaining half of the species, the frequency distributions suggest a descendant sequence of tertial moult (T 9—8—7), though again, there is considerable individual variation. Why the tertials should moult either descendantly or divergently is not, at present, clear.
Secondaries In some species which regularly renew the tertials during the partial postjuvenile moult, occasionally S 6, rarely S 5—6 or S 4—6, may be included as well (Motacilla alba, Phoenicurus ochruros, Sylvia atricapilla, Phylloscopus collybita, Parus caeruleus, P. major, Fringilla coelebs, Carduelis carduelis, C, chloris, C. spinus, Serinus serinus, Emberiza schoeniclus, see part II, Mester & Priinte 1982; Sylvia undata, S. melanothoraxy S. rueppelli, Roselaar in Cramp 1992, Svensson 1992). In Saxicola torquata and Cyanopica cyana up to five secondaries may be renewed (Gwinner et aL 1983, Fracasso 1985, de la Cruz et aL 1991, 1992). It seems that the renewal of some secondaries occurs as an extension of the tertial moult and some individuals with renewed secondaries also have eccentrically renewed primaries (see section 4.3.3). During the course of an extensive renewal of the primaries, the outermost secondaries are renewed as well as the innermost ones in Carduelis carduelis and Saxicola torquata (Mester & Priinte 1982, Fracasso 1985; see section 4.3.3).
Rectrices Within the feather tracts of the wing, the moult sequence of the partial postjuvenile moult may deviate from the basic sequence of the complete moult of adults.
Wing-coverts and alula The moult of the marginal coverts starts in their proximal part. The undermost row is the last to moult and is the most likely to be retained. The median coverts are moulted simultaneously, or else in a variety of sequences, In many species, the greater coverts which are to be renewed are shed almost simultaneously or in groups. Basically, a partial greater covert moult follows the descendant sequence starting with GC 9, i.e. the outer greater coverts remain unmoulted. GC 10 is usually moulted out of sequence after the adjacent greater coverts are already wellgrown. Thus, in species which renew only a few greater coverts, GC 10 is frequently retained out of sequence (e.g. Motacillidae, Fringillidae, see part II). However, in some other species, only GC 10 or GC 9+10 arc moulted and individuals with only a renewed GC 9 are virtually unknown (e.g. Phoenicurus phoenicurus^ Sylvia borin, Ficedula hypoleuca). Species which only occasionally moult their greater coverts sometimes show irregular patterns (especially frequent in Emberiza hortulana), although this is generally less frequent than in those adults which moult some greater coverts during a partial postbreeding moult. If only one alula feather is moulted, it is usually the smallest, or if two are moulted, the two smallest, thus conserving the descendant sequence.
Judging by the frequency distributions of renewed feathers after the completion of partial postjuvenile moult, rectrix renewal usually starts with the innermost one (Fig. 29). In about half of the species examined, the basic centrifugal sequence is followed quite strictly. As in the complete postbreeding and partial prebreeding moult, the three Motacilla species moult the rectrices convergently within each half of the tail (see also Herremans 1988a for Motacilla cinerea) and R 6 may occasionally be renewed alone. A convergent sequence of rectrix moult is also suggested for the majority of Carduelis carduelis (67% of the individuals with two new rectrices show renewed R 1 +6,33% R 1 +2; see also Mester & Prtinte 1982). In other Fringillidae and in Emberiza schoeniclus^ R 6 and R 2 are moulted in similar frequencies, but more often than R 3—5, suggesting a tendency for a convergent sequence (see also Westphal 1976). In all the species examined, considerable individual variation exists and it is often difficult to decide whether or not an unusual pattern is due to accidental rectrix loss or a genuine peculiarity. The rectrices are among those juvenile feathers which may already show signs of wear at fledging and which may be very worn after only a few months, if they have not been renewed. Thus, in those species which regularly moult only some of the rectrices, it might be an advantage to moult the most exposed central and outermost ones. However, those species which only rarely moult the rectrices and those which regularly renew them all (Parus major) have apparently not evolved this moult sequence.
Tertials
4.3.2 Relationship between wing-feather tract renewal during partial postjuvenile moult
The sequence of tertial moult during partial postjuvenile moult is very variable within and among species. In many, T 8 is shed first, followed
During partial postjuvenile moult, the relationship between the sequence and extent of feather renewal in the wing-feather tracts varies
Sequence ofpostjuvenile moult
33
Fig. 28. Percentage of individuals which have moulted a given tertial, after completion of the partial postjuvenile moult, divided into those with one, two or all three tertials renewed. Only those birds which moulted at least one tertial are included (N= sample size: own data).
between species. The postjuvenile moult of the wing usually starts with the marginal coverts, followed by the median coverts, the greater coverts and carpal covert, the alula, the tertials and rectrices. In Parus major, moult of the tertials and rectrices starts about three weeks after the beginning of postjuvenile moult (Dhondt 1973) and in Phylloscopus collybita about 11-12 days after (Norman 1991a). We chose to take the number of renewed greater coverts as a basis for comparing the extent ofpostjuvenile moult among the different wingfeather tracts. Generally, the extents of the postjuvenile moult of the various wing-feather tracts are correlated among each other, both within and among species. Within a species, individuals with lots of renewed greater coverts are more likely to have renewed feathers of the other tracts than individuals with only a few moulted greater coverts (data for the different species see part II). However, this interdependence is not very strict and a large number of different moult patterns are seen within a species. Interspecifically, some species renew some or all tertials, rectrices, carpal covert or alula feathers while moulting comparatively few greater coverts, while in other species birds with some of these feathers renewed have usually moulted all the greater coverts. Anthus trivialis, A.
pratensis and A. spinoletta may occasionally moult a tertial even when no greater covert is renewed and very often do so when only one greater covert is moulted, while e.g. Carduelis Moris only moults the tertials when all ten, rarely nine, greater coverts are renewed (see part II). Fig. 30 shows the mean number of postjuvenile tertials, rectrices, carpal coverts and alula feathers moulted in relation to the mean number of renewed greater coverts for 56 species. On average at least one tertial is renewed by species with more than 8.5 greater coverts moulted. Species with less than 8.5 greater coverts renewed usually moult the tertials only sporadically with the exception of three Anthus species, two Motacilla species, Phylloscopus collybita, Troglodytes troglodytes^ Turdtis merula, Garrulusglandariusand three Fringillidae (Fig. 30a). The relationship between the extent of the rectrix, carpal covert and alula feather moult and the greater covert moult is basically similar (Fig. 30bâ&#x20AC;&#x201D;d). Roughly the same species renew these feathers when few greater coverts are moulted, with the exception of the Anthus species. The juvenile marginal and median coverts are partly retained in those species which show only a limited postjuvenile moult (see part II). Apart from the marginal and median coverts, the innermost greater coverts (except GC 10) are most exposed when the wings are closed. It
34
The Moult During the First Year of Life
Fig. 29. Percentage of individuals which have moulted a given rectrix, after completion of the partial postjuvenile moult, divided into those with all six rectrices renewed, those with only one rectrix renewed, those with R 1 and R 2 renewed, those with R 1 and R 6 renewed and those with other combinations of renewed R. Only those birds which moulted at least one rectrix are included (N=sample size: own data).
therefore seems adaptive that, during a partial moult, all species renew the greater coverts in a descendant sequence, so that the innermost ones are moulted most frequently. The importance of the renewal of the other feathers of the wing relative to the extent of greater covert moult is shown in Fig. 30. The regular renewal of the tertials when, on average, less than about six greater coverts are moulted, may be related to the marked protective function of the tertials in these species (e.g. Motacillidae) and to their divergent moult sequence (see above). Why Fringilla coelebsand Sylvia curruca^ which, on average, moult more than eight greater coverts, only very rarely renew tertials remains unclear. The rectrices are regularly renewed together with a few greater coverts in Motacilla cinerea and M. alba which have the longest tails among small European passerines. Why some species renew the carpal covert and the alula feathers when only a few greater coverts are moulted is also a mystery. The frequent renewal of the conspicuously coloured alula feathers by Garrulus glandarius might be related to their signal function. The degree of regularity in their barred pattern may serve to
highlight the feather growth bars and, hence, display regular growth, good condition and high 'quality' of an individual bird (Hasson 1991).
4.3.3 Sequence of eccentric and other partial primary moults Some first-year birds renew some of their primaries during an extensive partial postjuvenile or partial first prebreeding moult (see sections 4.4.4 and 4.6.3). The focus and sequence of partial primary moults are still poorly known. Theoretically, partial primary moults may be generated by (a) a descendant sequence starting with P 1 (basic sequence interrupted at some stage), (b) a descendant sequence starting with a central primary, (c) an ascendant sequence starting with a central primary, (d) an ascendant sequence starting with P 9 or P 10, (e) a divergent sequence starting with a central primary, (f) a convergent sequence or (g) two or three foci and various sequences. In most cases, partial primary moult does not start with the innermost primary, but includes some central or outer primaries and has
Sequence ofpostjuveniie moult
35
Fig. 30. Mean number of moulted tertials (a), rectrices (b), carpal coverts (c) and alula feathers (d) in relation to the mean number of renewed greater coverts, after completion of the partial postjuvenile moult for 56 species (for data see part II). Key species are indicated by their abbreviated scientific names (see Fig. 34, p. 39).
been referred to as eccentric primary moult (Fig. 31).-In practice, this term has been used to describe a moult pattern of old inner and new central or outer primaries (cases b-e above). However, we suggest that the term eccentric primary moult should only be used for those partial primary moults which start somewhere in the centre of the primaries (cases b, c, e, possibly g) and not for those which follow a descendant sequence starting with P 1 (case a) or an ascendant sequence starting with P 9 or P 10 (case d). However, an ascendant partial primary moult, starting with P 9 or P 10 (case d), can only be distinguished from an eccentric primary moult which includes the outermost primaries when the focus or sequence can definitely be determined in actively moulting birds. The sequence of eccentric primary moult Is usually assumed to be descendant and in most cases, this assumption would be correct as confirmed by most studies on actively moulting birds, which start from a focus distally from P 1 (Sylvia melanocephala, Gauci & Sultana 1979; S. melanothorax, Roselaar in Cramp 1992; S. hortensis, Williamson 1968; Lanius senator, Bensch et al. 1991; L. collurio, Gwinner & Biebach 1977; L. isabeliinus, Stresemann & Stresemann 1972a; Carduelis carduelis^ Mester & Priinte 1982, W. Priinte pers. comm.; C. Moris, Westphal 1976, own obs.; Loxia curvirostra, Herremans 1988b). This finding is backed up by studies on Amercian passerines also (Miller 1928, Michener & Michener 1940, Taylor 1970, George
1973, Lloyd-Evans 1983, Stangel 1985, Rohwer 1986) as well as for Australian Meliphagidae (Dow 1973, Paton 1982). However, exceptions to the descendant eccentric primary moult can be found. Evans (1986) lists three first-year Sturnus vulgaris apparently moulting ascendantly from P 6 or 7 to P 1. There are also a few cases which suggest that an ascendant sequence may produce the pattern characteristic of an 'eccentric' moult. A small percentage of first-year Cyanopica cyana replace some outer primaries, very probably ascendantly starting with P 10 (de la Cruz et al. 1992, C. de la Cruz in lift.; Fig. 32). A first-year Certhia brachydactyla also moulted its primaries ascendantly (P 10â&#x20AC;&#x201D;8 half grown, P 7â&#x20AC;&#x201D;6 in pin, P 5â&#x20AC;&#x201D;1 old, possibly complete moult?; Copete & Senar 1990). Adult Locustella fluviatilis renew the outermost primaries ascendantly (see section 3.3.1). The peculiar primary moult pattern occurring in some first-year Cisticola juncidis, described as similar to an eccentric moult, actually consists of a divergent complete primary moult following an interrupted descendant primary moult started with P 1 (Gauci & Sultana 1981, C. Gauci in lift., cf. section 4.4.4). The examination of the distributions of renewed primaries in birds which have completed a partial primary moult reveals additional peculiarities of the moult sequence (Fig. 32). In all the Fringillidae, P 6 is renewed most often, suggesting at first sight a moult focus at P 6. However, Loxia curvirostra and some Carduelis chloris and C. spinus
36
The Moult During the First Year of Life
Fig. 31. Sylvia cantillans 2y 9 after partial prebreeding moult, 28 April. During the course of an extensive prebreeding moult, this bird renewed primaries 6-9 eccentrically. Note that the corresponding primary coverts have been retained.
may replace only one or a few inner primaries. Moreover, in C carduelis and, to a lesser extent, in C, Moris and C spinus, the more primaries that are renewed, the more proximal is the innermost renewed primary. If it is true that the sequence is invariably descendant, the focus of primary moult would, therefore, generally depend on the number of primaries to be renewed. This would agree with the finding that the focus of a basically descendant primary moult of adult cT Sturnus vulgaris shifts distally with increasing levels of experimentally administered testosterone which suppresses moult (Schleussner 1990). Thus, skipping the innermost primaries produces an eccentric moult where the focus is the more distal, the fewer the primaries that are to be renewed. This is precisely what seems to happen in the partial primary moult of Lanius senator (Fig. 32) for which a descendant sequence has indeed been observed (Bensch etal. 1991). In most individuals of the Fringillidae, the renewed primaries form an uninterrupted block of central primaries which may extend to P 9 or P 10. However, in some individuals some primaries not adjacent to a renewed primary are moulted, thus indicating two foci of primary moult (8.8% of Carduelis Moris showing partial primary moult, 8.7% of C cannabina, 5.4% of C. spinus, 0% of C. carduelis, 8.6% of Loxia curvirostra\ included in Fig. 32). These primaries are often either the innermost or the outermost (e.g. P 1-2+4-8 renewed in a Carduelis spinus, P 1+5-7 in a C Moris, P 3-7+9 in a C. Moris}. Furthermore, a few individuals of these species were found to have interrupted a primary moult which probably started with P 1 (not included in Fig. 32; see part II and Fracasso 1985 for Saxicola torquata). In Sylvia species which moult only some of the primaries, P 7â&#x20AC;&#x201D;9 are renewed most often, but the moult patterns are much more variable than in the Fringillidae. Individuals with only one renewed primary suggest that the focus may be at any primary (Fig. 32). Furthermore, individuals frequently have old primaries in between new ones (26.4% of those showing partial primary moult in Sylvia melanocephala, 22.0% in S. communisznd 12.0% in S. cantillans). Again, in addition to the central primaries, the outermost or innermost ones may often be renewed (e.g. P 1-2+6-8 renewed in a S. communis, P 1+7â&#x20AC;&#x201D;9 in a S. melanocephala). In some S. communis the primaries of three different blocks may be renewed (e.g. P 1 +6-7+9-10). Rarely, individuals of these Sylvia species may.moult only one to three innermost primaries (not included in Fig. 32). Thus it seems as if there might be a proximal, a central and a distal area within the primaries, each with a variable moult focus which can be activated alone or in combination with others. At present, nothing is known about the sequence of a partial primary moult which starts at two or three foci. There are a number of other characteristics of eccentric and other partial primary moults. As a rule, the primary coverts of the renewed primaries are either not moulted or are replaced independently of the
Fig. 32. Percentage of individuals which have moulted a given primary after completion of partial postjuvenile or first prebreeding primary moult out of those individuals (N)r which have moulted at least one primary. Individuals with only the innermost primaries renewed (descendant partial primary moult starting with P I ) are excluded, individuals showing two or three blocks of renewed primaries, including the innermost, are included. Except in Cyanopica cyana, the individuals are divided into those which renewed only one primary (hatched) and those which moulted more primaries (dotted). In Loxia curvirostra, Sylvia melanocephala and S. cantillans, P 10 was not assessed. Sources: Carduelis Moris: Westphal 1976, Mester & Priinte 1982, own data; C. cannabina: Mester & Priinte 1982, own data; C. spinus: own data; C. cardueli$\ Mester & Priinte 1982, own data; Loxia curvirostra: Herremans 1982, 1988b, own data; S. melanocephala: Gauci & Sultana 1979, Table 3 and own data; S. cantillans and S. c. communis: own data; Cyanopica cyana: de la Cruz et ai 1992; Lanius senator: Ullrich 1974, Roselaar in Cramp & Perrins 1993, own data, including six birds which have moulted all primaries.
Partialpostjuvenile moult in the breeding area corresponding primaries. This often helps to distinguish a partial postjuvenile primary moult from the suspended moult of adults, which generally includes the corresponding primary coverts in sequence with the primaries. The extent of an eccentric or other partial primary moult is not symmetrical on both wings in some 60% of cases. A partial postjuvenile moult which includes some primaries differs from the primary moult of adults in that it starts with the body-feathers and wing-coverts, not the primaries. The primaries are usually replaced together with the tertials, or shortly after when the wing-coverts and alula feathers are already growing or full-grown (Gauci &C Sultana 1979, own obs.). An eccentric moult is always combined with an extensive postjuvenile or prebreeding moult which includes all the bodyfeathers, marginal, median, greater and carpal coverts as well as at least part of the tertials, rectrices and alula. In many instances, some secondaries are also moulted, usually the innermost ones in a descendant sequence along with the tertials (Carduelis spinus> C. carduelis, C. Moris, Cyanopica cyana\ see part II and Westphal 1976, Mester & Priinte 1982, de la Cruz et al. 1992). In Carduelis carduelis and Saxicola torquata, the outermost secondaries may rarely be moulted during the course of an extensive partial primary moult (Mester & Priinte 1982, Fracasso 1985). During the first prebreeding moult, Lanius senator moults five to nine primaries and one to six secondaries (mean 3.5, all six secondaries by eight birds, N=53, own data). S 6 is always renewed and usually also some adjacent inner secondaries. In nine birds one or a few outermost secondaries were shed as well, suggesting a basically descendant sequence starting with S 6, and in a few birds, a convergent sequence. Most Sylvia melanocephala, S, communis and S. cantillans which moult some of the primaries also renew some or all of the secondaries (S. melanocephala: mean number of secondaries moulted 2.0, range 0-5, N=21; S. cantillans: mean 2.2, range 0-6, N=62; S, communis: mean 2.6, range 0â&#x20AC;&#x201D;6, N=38; own data; see also Gauci & Sultana 1979, p. 124 as well as S. melanothorax, Roselaar in Cramp 1992). In all three species, one to four innermost secondaries are usually moulted, as well as sometimes one to three outermost ones, suggesting a convergent sequence (see Gauci & Sultana 1979 and p. 124). Descendant, convergent and sometimes irregular sequences in partial secondary moult are also observed in adults (see section 3.2.3).
4.4 Partial postjuvenile moult in the breeding area With the exception of a few species, European passerines perform a partial postjuvenile moult in their first summer/autumn (moult cycles 3-9, 12-15 in Table 3). Whether the moult of some long-distance migrants after autumn migration or during a stopover should be regarded as part of, or as the entire, postjuvenile moult is discussed in section 4.6.2. In this section, only partial postjuvenile moults in late summer/autumn in the breeding area are treated. The main function of a partial postjuvenile moult appears to be the replacement of the loosely textured and often differently coloured juvenile body-feathers (see section 4.2) and of those feathers which would be too worn if retained until the next moult. Factors discriminating against a postjuvenile moult of the remiges soon after fledging include reduced flight capability and increased energetic and nutrient demands during the sensitive first phase of independence, as well as the lengthening of the postjuvenile moult duration. On the other hand, retaining the remiges for a year or more means that durable remiges must be grown during the nestling phase. Indeed, only birds with a suitably long period of time potentially favourable for moult renew some or all of the primaries, mostly during the terminal phase of the moult (see sections 4.4.4 and 4.5). The timing, duration and extent of the partial postjuvenile moult are extremely variable among and within species, as we shall see in the
37
remainder of this section. Its extent varies between species from virtual absence to include all the body-feathers, greater coverts, tertials, rectrices, alula, carpal covert (moult cycles 5-15 in Table 3) as well as part of the secondaries, primaries and primary coverts (moult cycles 3 and 4 in Table 3, treated in section 4.4.4). Even within a species, the postjuvenile moult may show all the transitional stages between a partial moult including only part of the wing-coverts and a complete moult (see sections 4.4.4 and 4.5). The categories of postjuvenile moult shown in Table 3 are thus not clearcut, and transitions between them occur. Because observations on the control of postjuvenile moult can largely explain the observed inter- and intraspecific variation, this information is given beforehand in the next section.
4.4.1 Variation in extent, timing and duration: experimental evidence of control of postjuvenile moult In many European passerines, moult is controlled by an endogenous, circannual rhythm which is more pronounced in tightly scheduled, long-distance migrants than in short-distance migrants (reviewed in Gwinner 1986). This rhythm is synchronized with the natural year by seasonal changes in the photoperiod and experimental changes in photoperiod can modify the annual moult programme (e.g. Dolnik & Gavrilov 1980, Noskov & Rymkevich 1985, Gwinner 1986). In birds kept under natural daylength, there are pronounced differences between species in the timing, duration and extent of the postjuvenile moult, as observed in free-living conspecifics. These species-specific differences are less pronounced, but still apparent when the birds are kept under a constant photoperiod (reviewed in Gwinner 1986). As shown in four species of Phylloscopus and two species of Sylvia warblers, postjuvenile moult starts earlier, overlaps more with the growth of the second set of juvenile body-feathers, is of shorter duration, ends earlier, includes more simultaneously growing feathers, is of lesser extent and is less variable in its timing in the early departing, long-distance migrants P. bonelli, P. sibilatrix, P. trochilus and S. borin than in the late departing, short-distance migrants P. collybita and S. atricapilla (Gwinner 1969, Berthold etal. 1970, Gwinner etaL 1971). The timing, extent and duration of the postjuvenile moult also differ between populations of the same species. In Sylvia borin, S. atricapilla and Phylloscopus trochilus kept under natural photoperiods, postjuvenile moult starts earlier and is generally of shorter duration in northern than in southern populations. These differences persist when birds from different populations are held under the same constant photoperiod, suggesting an underlying genetic control of postjuvenile moult (Gwinner etaL 1972, Berthold etaL 1974, Berthold 1977, Gwinner 1979, Berthold & Querner 1982b). Indeed, hybrids of two populations of S. atricapilla and of Saxicola torquata with different natural timing of the postjuvenile moult showed an intermediate timing and moult duration. The postjuvenile moult is thus partly controlled by an innate, genetically fixed time prograjnme (Berthold & Querner 1982b, Gwinner & Neusser 1985). This ultimate genetic time programme can be modified by the prevailing photoperiod. In several species, it can be shown that latehatched individuals held under natural daylength, moulted at an earlier age and more rapidly than early-hatched conspecifics of the same population; likewise, birds held under a constant short daylength moulted at an earlier age and more rapidly than birds of similar hatching date held under long daylength (e.g. Berthold et al 1970, 1972, Gwinner et al 1971, Dolnik & Gavrilov 1980). Noskov & Rymkevich (1985) found this dependence of postjuvenile moult on photoperiod in almost all of the 42 European passerine species examined. According to their analysis, postjuvenile moult proceeds normally only within a certain interval of daylength, specific to the species and population. If the daylength is too short for a given species and population, moult stops.
38
The Moult During the First Year of Life
The start of moult is largely determined by the hatching date. In species with a long breeding season, photoperiod is capable of modifying the onset of moult to a greater extent than in species with a short breeding season. For instance in Emberiza citrinella, the maximum, probably genetically controlled, age at which postjuvenile moult starts is 60 days, which cannot be increased by increasing daylength. Under short days of 14 hours, postjuvenile moult starts at the age of 20 days. In E. hortulana? however, the maximum age at which postjuvenile moult starts under a long day regime is only 25 days; the minimum, prompted by short days is 18 days (Noskov &: Rymkevich 1985; see also Gwinner etal. 1971). These experimental results show that the controlling programme is broadly genetically fixed and adapted to the population. It can be modified to a certain extent by photoperiod (though other factors which may modify postjuvenile moult are treated below). Late-hatched birds moult young and fast and can at least partly catch up and finish postjuvenile moult only shortly after their early-hatched conspeciflcs. The following two sections will show that the partial postjuvenile moult of free-living birds is also governed by these rules,
4.4.2 Interspecific variation in timing and extent Timing and duration The postjuvenile moult may start immediately after fledging (e.g. Sylvia nisoria, Glutz & Bauer 1991; Ficedula hypoleuca, Muscicapa striata, Rymkevich 1990) or more than two months after leaving the nest (e.g. Cardueiis spinus, lovchenko & Smirnov 1987; Loxia curvirostra, see p. 182; Carpodacus erythrinus and Emberiza a. aureola see
section 4.6.2). Intense postjuvenile moult does not generally overlap significantly with autumn migration or the cold season, but overlaps with low intensity moult are more frequent than in the postbreeding moult of adults. In many species, low intensity postjuvenile moult may continue during the first stages of migration, as for instance in Luscinia svecica (Lindstrom et al. 1985), Acrocephalus scirpaceus (Herremans 1990b), Phylloscopus trochilus (Norman 1981) and Motacilla flava (Dittberner & Dittberner 1987). In the long-distance migratory hirundines, moult of the body-feathers occurs at least during the first part of the autumn migration (see part II) and Ptyonoprogne rupestris moults slowly during the entire autumn and winter (Elkins & Etheridge 1977). Emberiza schoenicluswzs found in active body-feather moult as late as December in S France (Bell 1970). Despite these overlaps between moult and autumn migration, the postjuvenile moult is generally fitted within the period between fledging and migration or the onset of the cold period (species delaying postjuvenile moult until after autumn migration are discussed in section 4.6.2). The data available at present reveal that the age at which postjuvenile moult starts is linearly related to the time available, expressed as the difference between the mean fledging date and either the peak autumn migration date in Central Europe, or the onset of winter (Fig. 33a). Hence, species with a long period available for moult start postjuvenile moult at a later age. The duration of the postjuvenile moult is also related to the time available, but levels off at about 56 days (Fig. 33b). Thus, none of the species included in Fig. 33 extends the postjuvenile moult over more than 45-70 days, even though more time may be available. Hence, the age at which postjuvenile moult is completed is never more than about 90-130 days (Fig. 33a). The slopes of the relationships presented in Fig. 33 show that as more time is available for moulting, the onset of moult is only slightly postponed
Fig. 33. Onset and completion (a) and duration (b) of partial postjuvenile moult of European passerine species during summer/autumn in relation to the time potentially available for moult, i.e. the time between fledging and peak autumn migration or the onset of winter. Data on the onset and end (relative to the bird's age in days since hatching) and duration of postjuvenile moult are taken from the summaries in Ginn & Melville (1983), Glutz & Bauer (1985, 1988, 1991) and Rymkevich (1990, data from early-hatched birds) as well as from Norman (1981, 1990a, 1991a), Boddy (1983), Rymkevich (1983), Dittberner & Dittberner (1987, 1989), lovchenko & Smirnov (1987) and Rymkevich &c Pravosudova (1987). The time available for moulting between fledging and peak autumn migration is the peak date of autumn migration (Jenni 1984; accurate to within five days) minus the peak date of laying (accurate to within five days), minus the mean incubation and nestling period (Glutz & Bauer 1985, 1988, 1991 and other references; if possible using data from the area where the moult data were collected). For mainly sedentary species, the peak autumn migration was repkced by the onset of winter, arbitrarily set at the beginning of November. Since data on laying as well as on postjuvenile moult are often not very accurate, the graphs presented can only give a general picture. Linear regressions indicated are: onset of postjuv moult: y=0.330x+278, r=0.81, N=44, P<0.001; end of postjuv moult: for x<100 days: y=0.808x+3.43, r=0.74, N=17, P=0.007, for x>100 days: y=0.492x+36,46, r=0.6l, N=22, P=0.002; duration of postjuv moult: for x< 100 days: y=0.74lx-18.4l, r=0.74, N=17, P<0.001. The mean duration (Âą s.d.) of the 24 values outside the regression line is 56.3 Âą 6.4 days. The species included are: Anthus campestris (onset only), A. trivialis (onset only), A. s. spinoletta, Motacilla flava, M. alba, Cinclus cinclus, Troglodytes troglodytes (duration only), Prunella modularis, Erithacus rubecula, Luscinia luscinia, L. megarhynchos, L. svecica (onset only), Pkoenicurus phoenicurus, Saxicola rubetra (onset only), Oenanthe oenanthe, Turdus torquatus alpestris (onset only), T. merula, T> pilaris, T. philomelos, T. iliacus, Acrocephalus scirpaceus, Sylvia nisoria, S. curruca, S, communis, S. borin, S. atricapilla, Phylloscopus bonelli, P. sibilatrix, P. collybita, P. trochilus, Regulus regulus, R. ignicapillus, Muscicapa striata, Ficedula hypoleuca, Parus caeruleus, P. major, Fringilla coelebs, F. montifringilla, Cardueiis chloris, C. carduelis, C. spinus, C. flammea, Pyrrhula pyrrhula (duration only), Emberiza citrinella, E, hortulana, E. schoeniclus.
Partial post juvenile moult in the breeding area relative to fledging (by 0.33 days per day increase in available time), but the duration is increased tremendously (by 0.74 days) up to about 50-60 days. When more time is available for moult, the duration of postjuvenile moult remains more or less constant, though its onset is further postponed. As shown for Sylvia atricapilla and Phylloscopus collybita, species which start their postjuvenile moult only a few weeks after fledging may disperse while in their juvenile plumage, or at the beginning of the postjuvenile moult, before becoming more sedentary and performing the postjuvenile moult before the onset of autumn migration (Jenni 1984, Wolf 1987, Norman 199la). In Sylvia atricapilla, the area visited during the pre-moult dispersal is often the subsequent breeding place (Wolf 1987). Those species which undertake the postjuvenile moult soon after fledging and within a short space of time, achieve this by moulting only a limited number of feathers (see below), by growing many feathers simultaneously, by overlapping the completion of the juvenile plumage and the postjuvenile moult (Fig. 23) and by retaining the second set of juvenile feathers. Species moulting at a later age start moult only several weeks after completing the juvenile plumage and renew more feathers, including the second set of juvenile feathers (Gwinner 1969, Berthold etai 1970, Rymkevich 1990).
39
Extent The extent of the postjuvenile moult in the breeding area can be expected to relate to the time available for moulting. However, there is no simple linear relationship. For the moult of the greater coverts, carpal covert, alula feathers, tertials and rectrices, there appears to be a maximum possible extent of postjuvenile wing-moult for any given available time for moulting (Fig. 34). This maximum is, however, only attained by a few species, and many with long potential moult periods only perform a rather limited postjuvenile wing-moult. The time available for moulting is generally short in long-distance migrants (less than 100 days in Fig. 34) and their postjuvenile moult is therefore usually less extensive than in short-distance migrants or sedentary species. Some long-distance migrants do not moult at all before the autumn migration and merely complete the juvenile plumage with the second set of juvenile feathers (Acrocephalus palustris according to Dowsettâ&#x20AC;&#x201D;Lemaire 1981; A. $choenobaenusy Griill & Zwicker 1982; A. paludicola, Roselaar in Cramp 1992; Locustella luscinioideSy Miiller 1981; Emberiza a. aureola, Stresemann & Stresemann 1969a; Carpodacus erythrinus, Bozhko 1980). Others moult only a part of the body-feathers (hirundines) as well as some
Fig. 34. Mean extent of partial postjuvenile wing-moult during summer/autumn in relation to the time potentially available for moult (see Fig. 33) for 55 European passerine species. The mean extent of postjuv moult of a species was calculated by summing the mean number of greater coverts, tertials, rectrices, alula and carpal coverts replaced on one wing (data presented in part II) weighted by factors accounting, approximately, for the relative mass of the different feathers. Based on Newton (1966), these values are 1 for greater covens and carpal covert, 3 for tertials, 6 for rectrices and 0.5 for alula feathers. Therefore, the maximum possible extent is 56.5. This procedure is only approximate since the body-feathers, marginal and median coverts, secondaries and primaries are not included and because the feather mass factors differ between the individual feathers of a tract and between species (cf. Herremans 1988a). A.cam = Anthus campestris, A.pra = A. pratensis, A.sci = Acrocephalus scirpaceus, A.spi = Anthus spinoletta, A.tri = A. triviality C.can = Carduelis cannabina, C.car = C. carduelis, C.chl = C. chloris, C.coc = Coccothraustes coccothraustes, C.fla = Carduelisflammea, C.spi = C spinus, D.urb = Delichon urbica, E.cia = Emberiza cia, E.cit = E. citrinella, E.hor = E, hortulana, E.rub = Erithacus rubecula, E.sch = Emberiza schoeniclus, F.coe = Fringilla coelebs, F.hyp = Ficedula hypoleuca, F.mon = Fringilla montifringilla, G.gla = Garrulus glandarius, H.ict = Hippolais icterina, H.rus = Hirundo rustica, L.col = Lanius collurio, L.meg = Luscinia megarhynchos, L.sve = L. svecica, M.alb = Motacilla alba, Mcin = M. cinerea, M.fla = M. flava, M.str = Muscicapa striata, O.oen = Oenanthe oenanthe, P.atr = Parus ater> P.cae = P. caeruleus, P.maj = P.major, P.mod = Prunella modularis, P.col = Phylloscopus collybita, P.och = Phoenicurus ochruros, P.pho = P. phoenicurus, P.tro = Phylloscopus trochilus, R.rip = Riparia riparia> S.atr = Sylvia atricapilla, S.bor = S. borin, S.cit = Serinus citrinella, S.com = Sylvia communis, S.cur = S. curruca, S.eur = Sitta europaea, S.rub = Saxicola rubertra, S.ser = Serinus serinus, T.ili = Turdus iliacus, T.mer = T. merula, T.phi = T. philomelos, T.pil = T. pilaris, T.tor = T, torquatus alpestris, T.tro = Troglodytes troglodytes, T.vis = Turdus viscivorus.
40
The Moult During the First Year of Life
marginal and median coverts (e.g. Sylvia nisoria, Rymkevich 1990; Lanius collurio, Oriolus oriolus, many Emberiza hortuiana and Anthus campestris, see part II; possibly some other species, e.g. certain Acrocephalus and Hippolais warblers, in which juvenile and postjuvenile body-feathers are difficult to distinguish). In other long-distance migrants, all the body-feathers, marginal and median coverts are regularly moulted, but none (e.g. most Oenanthe oenanthe) or only the innermost one or two greater coverts (e.g. most Phoenicurus phoenicurus, Sylvia borin, Muscicapa striata, Ficedula hypoleuca). Only a few long-distance migrant species regularly moult all the body-feathers, several of the greater coverts and occasionally some tertials or rectrices (e.g. Motacilla flava, Luscinia megarhynchos, Sylvia curruca, cf. Fig. 30). Short-distance migrants and sedentary species with a longer potential moult period (more than 100 days in Fig. 34) usually moult all the body-feathers, the marginal and median coverts as well as part of the greater coverts. In some species, some tertials are also regularly moulted (e.g. Sylvia atricapilla) as well as some rectrices (e.g. Phylloscopus collybita, Emberiza schoenidus, Carduelis chloris, Coccothraustes coccothraustes). In Parus major, the partial postjuvenile moult regularly includes all the wing-coverts, tertials and rectrices. Some species occasionally also renew the innermost, rarely the two or three innermost, secondaries (e.g. Motacilla alba, Phoenicurus ochruros, Sylvia atricapilla, Phylloscopus collybita, Parus major, P, caeruleus, Fringilla coelebs, Carduelis carduelis, C. chloris, C. spinus, Serinus serinus, Emberiza schoenidus, see part II; Sylvia undata, S. melanothorax, S. rueppelli, Roselaar in Cramp 1992, Svensson 1992). Saxicola torquata and Cyanopica cyana occasionally renew up to five secondaries (Gwinner et al, 1983, Fracasso 1985, de la Cruz ^rf/. 1991, 1992). However, there are a number of species with a rather long potential postjuvenile moult period in summer/autumn which only moult a few feathers (Fig. 34). At present, it is difficult to explain why some species do not moult as many feathers as do others with a comparable potential moult period. Possible explanations may include the following factors. In some species, it may be less important for a first-year bird to completely attain the adult coloration. The retained juvenile feathers might be durable enough to last until the next moult, either because they face little exposure to wear or because durable feathers could be grown in the nest. However, in species with long moult periods (> 100 days in Fig. 34), there is no clear relationship between the extent of the postjuvenile moult and the occurrence of a prebreeding moult, unlike long-distance migrants (see section 4.6.1). In some species, a tight energy and nutrient regime might prevent an extensive postjuvenile moult. In this respect, it is noteworthy that the alpine and subalpine species Serinus citrinella, Carduelis flammea, Turdus torquatus and Anthus spinoletta moult fewer feathers than comparable species occurring mainly in lowlands. Their harsher montane environment may impose more stringent energy and nutrient stresses. The occasional renewal of the innermost one or few secondaries during a partial postjuvenile moult in summer/autumn is difficult to explain (in contrast to the first prebreeding moult, see section 4.6.3). It constitutes an extension of the renewal of the tertials, perhaps because S6 wears while it takes over the protective function of the longest tertial during its renewal.
4.4.3 Intraspecific variation in timing and extent Variation with hatching date Many studies on free-living birds confirm the experimental evidence (see section 4.4.1) that birds hatched late in the season start their postjuvenile moult at an earlier age, moult more rapidly and renew fewer feathers than early-hatched young of the same population. Late-hatched birds of species which generally start postjuvenile moult at an early age, can advance the onset of moult by only a few
days relative to early-hatched young (Berthold et al. 1970, Noskov & Rymkevich 1985, Rymkevich 1990). In species which generally start their postjuvenile moult at a later age, late-hatched birds can advance the moult by several weeks and may start it before the juvenile plumage is completed, as do long-distance migrants (e.g. Pyrrhula pyrrhula, Newton 1966; Fringilla coelebs, Dolnik & Gavrilov 1980; Carduelis flammea, Boddy 1983; Turdus iliacus, Chochlowa et al. 1983 after Glutz & Bauer 1988; Sylvia atricapilla, Berthold et al. 1970; Carduelis flammea, Boddy 1983; Parus major, Dolnik & Blyumental 1967, Dhondt 1973; see Rymkevich 1990 for further species). The duration of the postjuvenile moult of late-hatched birds is generally considerably shorter than in early-hatched birds (e.g. Emberiza schoenidus, Haukioja 1969, Bell 1970; Emberiza spp., Rymkevich 1983; Turdus iliacus, Chochlowa et aL 1983 after Glutz & Bauer 1988; Fringilla coelebs, Dolnik & Blyumental 1967, Dolnik & Gavrilov 1980; Sylvia borin and S. atricapilla, Berthold et al. 1970; see also Rymkevich 1990 for many species), but not in Sylvia nisoria with its already very short moult duration (Rymkevich 1990). Early-hatched Motacilla alba, for instance, moult within 60 days, late-hatched within 42 days (Baggott 1970), early-hatched Sylvia communis within 45 days, late-hatched within 36 days (Stolbowa & Musaew 1987 after Glutz & Bauer 1991). By starting the postjuvenile moult earlier and by moulting more rapidly, late-hatched birds catch up with early-hatched birds either partly (e.g. Emberiza schoenidus, Bell 1970, Parus major, Dhondt 1973; Sylvia borin and S. atricapilla, Berthold et al. 1970) or completely (e.g. Turdus iliacus, Chochlowa et al. 1983 after Glutz & Bauer 1988; Fringilla coelebs, Dolnik & Gavrilov 1980). The shorter moult duration of late-hatched birds is achieved first by moulting more feather tracts and feathers simultaneously (e.g. Dolnik & Blyumental 1967, Berthold et al. 1970, Chochlowa et al. 1983 after Glutz & Bauer 1988). Second, the extent of the moult is reduced, something most easily observed in species which normally include some feathers of the wing in the moult (see part II). A reduction in the extent of greater covert moult of late-hatched birds was observed in Pyrrhula pyrrhula (Newton 1966), Sylvia atricapilla (Norman 1990a, Rymkevich 1990), S. communis (Norman 1990a), Erithacus rubecula> Sylvia curruca, Ficedula hypoleuca, Fringilla montifringilla (Rymkevich 1990), in the extent of alula and greater covert moult in Parus major (Dhondt 1973, Reith & Schmidt 1987, Rymkevich 1990, Gosler 1991) and in the extent of greater covert, tertial and rectrix moult in Motacilla alba (Baggott 1970, Rymkevich 1990), M. flava (Dittberner & Dittberner 1987), Troglodytes troglodytes (Hawthorn 1974), Parus caeruleus, Carduelis chloris, C. spinus and C. carduelis (Rymkevich 1990). Early-hatched Sylvia melanocephala perform a complete postjuvenile moult, or include many remiges, while late-hatched young do not generally moult any remiges (Gauci & Sultana 1979). On the other hand, Rymkevich (1990) reports a similar extent of moult in early- and late-hatched Sylvia borin and S. communis which generally perform a postjuvenile moult of limited extent within a short period of time. There are very few studies investigating the effect of variation in timing and extent of postjuvenile moult within a population on future events in the life of the bird and on its survival. For instance, Dhondt (1973) observed that late-hatched Parus major are still moulting when autumnal territorial behaviour begins and are more likely to emigrate. He suggests that the disadvantages of moulting might cause subordination during autumnal contests in this species. Furthermore, one might suppose that an extensive postjuvenile moult may be advantageous in two ways. First, in many species it reduces the juvenile plumage characters, which might be of behavioural advantage in contests and, in species without an extensive prebreeding moult, in the first reproductive season. Second, an extensive renewal of the juvenile feathers might significantly increase the structural quality of the plumage.
Partialpostjuvenile moult in the breeding area
Differences between populations Apart from the experimental evidence on Sylvia borin, S, atricapilla and Phylloscopus trochilus (see section 4.4.1), there is very little data on the timing and duration of postjuvenile moult in free-living populations in different geographical areas. It has been shown for Fringilla coelebs that the postjuvenile moult is shorter in northern than in southern populations (Dolnik & Blyumental 1967, Gavrilov 1979 after Ginn & Melville 1983). Russian Phylloscopus collybita commence postjuvenile moult at 25—45 days old and do not renew the second set of juvenile feathers (Rymkevich 1990), In contrast, British birds are 53 and captive German birds 68 days old at the start of moult and both renew the second set of juvenile feathers (Gwinner 1969, Norman 1991a). On the other hand, many species are known to differ in the extent of postjuvenile moult between different populations. Northern populations usually perform a less extensive moult than more southern ones, while populations occurring at similar latitudes do not differ in the extent of the moult (see Motacilla flava, M. alba, Erithacus rubecula, Turdus merula, Phylloscopus trochilus, Pants major, P. ater, Carduelis Moris, C. carduelis, C. spinus, Serinus citrinella, Emberiza schoeniclus in part II). While this seems to be an adaptation to the shorter time available between fledging and migration in northern populations, it is unclear to what extent the photoperiodic and innate genetic differences (cf. section 4.4.1) contribute respectively to the lesser extent of postjuvenile moult of northern populations. Despite their living at different latitudes, the extent of the postjuvenile moult of Turdus torquatus torquatus and T. t. alpestris does not differ (p. 107), possibly due to their similar timing of breeding and, consequently, similar period available for moult in both the Alpine and the Scandinavian subspecies. Some observed differences in the extent of postjuvenile moult between populations do not fit the general latitudinal pattern. For example, why should Parus major and P. caeruleus moult fewer feathers on the wing in Great Britain than in central Europe? Furthermore, slight differences in the extent of moult of Parus major have been found between nearby sites (Reith & Schmidt 1987): urban birds renewed more alula feathers and greater coverts than rural birds, and birds hatched at higher altitudes moulted alula feathers less frequently than lowland birds. This can be explained, at least partly, by differences in hatching dates between the sites.
Differences between the sexes and effects of energetic and nutrient stress $ apparently perform a more extensive postjuvenile moult in summer/autumn than ? in at least 13 species of European passerines. In d of species with a generally restricted moult, more juvenile greater coverts are lost (Phoenicurusphoenicurus, Ficedula hypoleuca\ see part II, Karlsson et ai 1986b). 3 of species with a moderate extent of moult replace more greater coverts, tertials, rectrices, carpal covert or alula feathers (Motacilla alba, Sylvia atricapilla, Parus major, Carduelis carduelis, C. spinus, C. cannabina, Serinus citrinella, Pyrrhula pyrrhula, Loxia curvirostra, Emberiza schoeniclus', see part II, Newton 1966, Baggott 1970, Dhondt 1973, Pettersson 1981, Herremans 1982, 1991, but not 1988b, Reith & Schmidt 1987, Gosler 1991). In cJ Cyanopica cyana, whose moult is extensive, more juvenile primaries, secondaries, primary coverts and rectrices are lost (de la Cruz et al. 1991). Of the species examined (see part II), the mean difference between cT and $ is 0.3—1.0 greater coverts, 0.2—0.6 tertials and 0.16—0.5 rectrices. Haukioja(1969) suggests that the postjuvenile moult of 2 Emberiza schoeniclus takes about 10 days less than in d. In three other species, 6 moult slightly more feathers on the wing than $, but the difference is not significant (Parus caeruleus, Carduelis Moris, Serinus serinus; part II, Frelin 1977). In six species, there is no difference in the extent of moult between the
41
sexes (Erithacus rubecula, Turdus torquatus alpestris, T. merula, T. pilaris, Fringilla coelebs, F. montifringilla; part II, Baillie & Swann 1980, Karlsson et al. 1986a). No European passerine is known in which $ perform a more extensive postjuvenile moult than d. Why there should be a difference in the extent of postjuvenile moult between the sexes is largely unexplained. It appears that a sexual difference in moult extent occurs in species in which the greater coverts and tertials are generally more brightly or conspicuously coloured. Thus, d with important signal coloration on the greater coverts and tertials might gain more by investing in postjuvenile moult than $?, in order to achieve a more adult-like plumage for contests during winter and the following breeding season. However, this explanation can hardly apply to Ficedula hypoleuca and Phoenicurusphoenicurus, in which the average difference between cT and ? is very small and concerns inconspicuously coloured greater coverts (see part II). Furthermore, d performing a prebreeding moult of greater extent than the postjuvenile moult do not gain any obvious advantage for the next breeding season from moulting more feathers during the postjuvenile moult. Gosler (1991) showed that the extent of greater covert moult in ? Parus major is correlated with a measure of their protein reserves in the following winter. He concluded that the extent of greater covert moult is determined directly by protein stress, or by a correlate of protein stress, during moult which also has an effect on protein reserves during winter. One can argue that such a correlate might be hatching date resulting in a shortened postjuvenile moult due to short daylength; protein stress due to the subdominant status of late-hatched birds may also play a role. If protein stress or energetic constraints during moult directly affect the extent of postjuvenile moult, this may also explain the differences in the extent of moult between years (as observed in Parus major and P. caeruleus•; Spencer & Mead 1978a, Reith & Schmidt 1987), between nearby populations (as observed in Parus major, Reith & Schmidt 1987), between habitats and between dominant and subdominant individuals and sexes. There is, however, no conclusive study so far known to us which clearly demonstrates energetic or nutrient effects on the extent of postjuvenile moult in passerines.
Intraspecific variation in the extent of postjuvenile moult during the course of the non-breeding season and between wintering sites The extent of completed postjuvenile moult often shows striking seasonal trends, especially during autumn migration (e.g. Herremans 1988a, 1991, graphs in part II). Such birds with different moult extents migrate through a study site at different times. There is generally a decrease in the extent of greater covert moult during autumn migration in all species examined (see part II, Hereward 1979, Karlsson et al. 1986a, Herremans 1988a, 1991, Pettersson et al. 1990), except in Phoenicurus phoenicurus, Phylloscopus trochilus and Ficedula hypoleuca, which always show a limited extent of greater covert moult. Judging by the discussion so far, this decrease may be due to the later migration of late-hatched birds or birds from northern origin, or of $, all of which usually perform a less extensive moult, or a combination of factors (cf, Herremans 1988a). Furthermore, in some species, differences in the extent of postjuvenile moult have been found between populations in different wintering sites (e.g. Swann & Baillie 1979, Pettersson et al. 1990). The question is whether these differences can be related to the various possible causes of reduced moult extent, thereby giving indications of the sexual, age-specific or geographical composition of migrant or wintering bird populations. Of the factors known to influence the extent of moult (hatching date, geographical area and sex), geographical area and sex can be excluded when investigating a sexable species of limited distribution. This is the case in the Alpine population of Serinus citrinella. This species shows a
42
The Moult During the First Year of Life
distinct decrease in the extent of greater covert moult (Fig. 512) at the Alpine pass of Col de Bretolet during the course of autumn migration, which takes place from mid-September to early November (Jenni 1984). The number of moulted greater coverts correlates in both sexes with a measure of postjuvenile developement, derived from the degree of skull pneumatization and assumed to be related to hatching date (Table 4), but not with body mass or wing-length. This suggests that hatching date is an important factor causing the variation in the extent of greater covert moult and that early-hatched birds migrate through the study site earlier than late-hatched birds. Birds examined on migration or in the wintering areas may also vary in the extent of their moult due to differences between geographical populations. This can be assessed when an independent characteristic indicating the geographical origin of migrants is available. In Sylvia atricapilla, wing-length (or alternatively feather-length of P 8, Jenni & Winkler 1989) increases from southwest to northeast (Klein etai 1973, own unpubl. data). The number of moulted greater coverts is again correlated with the measure of hatching date in both sexes, but also negatively with feather-length, suggesting that both hatching date and geographical origin partly explain the variation in moult extent (Table 4). According to the analysis of wing-length, northern populations of S. atricapilla move through central Europe during the early part of the autumn migration, before most of the central European populations have started (Klein etal. 1973, Turrian & Jenni 1989). Thus, in Sylvia atricapilla, the number of moulted greater coverts decreases during autumn migration (Fig. 356) despite the early passage of northern birds, which have slightly fewer greater coverts moulted. This indicates that hatching date is probably the predominant factor determining the decrease of greater covert moult during autumn migration. In the study
Table 4. Mean number of moulted greater coverts of S and 9 Serinus citrinella and Sylvia atricapilla for selected dates at which skull pneumatization score 2 (see appendix) was reached (date of skull 2) estimated from a generalized linear model analysis. From retraps, the intervals between successive skull pneumatization scores was estimated to be 23 and 16 days for the two species, respectively. Using this information, the date at which skull pneumatization score 2 was attained was estimated for each individual and was assumed to be a measure of hatching date. For Serinus citrinella, analysis by generalized linear models revealed that the number of moulted greater coverts is significantly dependent on the date of skull 2 (t = -11.79) and sex (t = -7.08), but not on body mass or length of P 8 (as a measure of wing-length, Jenni & Winkler 1989) (N= 695). For Sylvia atricapilla, the number of moulted greater coverts was significantly dependent on the date of skull 2 (t = -10.85), sex (t = -3.54) and feather-length of P 8 (t = -2,44) (N=658). Serinus citrinella Date of skull 2
21 May 20 June 20 July 19 August 8 September
Mean number of moulted greater coverts
8
9
9.2 8.6 7.8 6.8 5.5
8.8 8.1 7.1 5.8 4.4
Sylvia atricapilla Date of skull 2
Mean number of moulted greater coverts Feather-length 50 mm
16 June 9 July 3 August 27 August 10 September
9.9 9.8 9.5 9.1 8.2
9.8 9.7 9.3 8.7 7.7
Feather-length 60 mm
9.8 9.5 9.0 8.2 6.8
9.7 9.3 8.7 7.6 6.0
by Herremans (1991), a similar relationship between the extent of greater covert moult and wing-length was found in $ S. atricapilla, although the relationship with skull pneumatization was only very weak (skull data not transformed to give an indication of hatching date). In Troglodytes troglodytes, the number of greater coverts moulted also decreases during the autumn migration (Fig. 155), while wing-length increases. Furthermore, there is a significant relationship between the number of greater coverts moulted and wing-length, northern populations having on average slightly longer wings than southern populations. This suggests that northern populations migrate through Switzerland later and have fewer greater coverts moulted than do southern populations (Jenni & Winkler 1983). In the absence of any information on hatching date, it remains unclear whether geographical origin genuinely influences the extent of greater covert moult or whether it is an artefact of the effect of hatching date due to the later breeding of northern populations. A reduced extent of postjuvenile moult in late-hatched compared to early-hatched British Wrens was suggested by Hawthorn (1971, 1974). Even when skull pneumatization can be used to assess the hatching date and wing-length to suggest the geographical origin, it remains difficult to judge the relative importance of hatching date and geographical origin as factors causing a change in moult extent. This is because skull pneumatization and wing-length are only approximate indicators of hatching date and geographical origin and are probably accurate to different degrees. From the available evidence, however, it is probable that late-hatched birds migrate later in autumn than earlyhatched birds, both within and between populations. Of the species wintering in Switzerland, the number of postjuvenile greater coverts is lower during the beginning of winter at least compared to the end of autumn migration in Troglodytes troglodytes (see Jenni & Winkler 1983), Erithacus rubecula, Turdus pilaris, Fringilla coelehs, F. montifringilla, Carduelis Moris and C. spinus (see part II). It is lower than the average during autumn migration in Turdus merula and Pyrrhulapyrrhula (see part II). This suggests that birds wintering in Switzerland are mainly of northern origin and/or late-hatched. In these species, the number of postjuvenile greater coverts increases during the spring, probably due to the return of early-hatched birds, or of those from central European populations. In birds caught during spring migration, no seasonal trend of the extent of postjuvenile moult has been observed (Erithacus rubecula, Karlsson et ai 1986a, p. 91; Sylvia atricapilla, p. 130). Thus, there seems to be no sequential passage of second-year birds correlated to hatching date as in the autumn. Furthermore, the extent of postjuvenile moult during spring is approximately equal to the mean over the entire autumn migration in all species examined (Troglodytes troglodytes, Erithacus rubecula, Phoenicurus ochruros, Turdus merula, T, pilari$> T. philomelos, Sylvia atricapilla, Fringilla coelebs, Carduelis chloris, C, spinus, Pyrrhula pyrrhula; see part II). In wintering populations, the extent of postjuvenile moult may differ between sites. In Turdus merula wintering in Scotland, birds in rural roosts showed a less extensive postjuvenile moult than those in urban roosts. This was attributed to there being more continental immigrants in rural roosts (Swann & Baillie 1979). Wintering Parus ater from England also showed differences in the extent of moult, probably due to a lesser extent of moult in northern and eastern populations (Christmas etal. 1989). Pettersson etal. (1990) showed that Erithacus rubecula wintering in the E Mediterranean had fewer greater coverts moulted than birds wintering in the W Mediterranean. Differences between years in the extent of postjuvenile moult have been observed in some migrants (Motacilla flava, Hereward 1979; Parus major, Pettersson 1981; Parus ater, p. 146). This may be due to different hatching dates between years, other differences between years acting on the same population or a variation in geographical origin of the migrants. Annual variations and differences between nearby sites (sometimes due to differences in the timing of breeding) further
Partialpostjuvenile moult in the breeding area
complicate the use of moult extent in determining the origin of birds (see e.g. Pettersson 1981, Reith & Schmidt 1987).
4.4.4 Partialpostjuvenile primary moult in the breeding area Partial renewal of the primaries during the postjuvenile moult in the breeding area (moult cycles 3 and 4 in Table 3) has only recently been studied in European passerines. Its occurrence and significance, therefore, are still poorly known. In all species in which a postjuvenile moult includes part of the primaries, most, or at least a significant proportion of individuals perform a partial postjuvenile moult which does not include any primaries (moult cycles 5 and 6 in Table 3), or a complete postjuvenile moult (moult cycle 1 in Table 3). In Sylvia melanocephala, S. melanothorax, S. conspicillata, Carduelis chloris, Loxia curvirostra and possibly others, the entire range of possibilities from a partial postjuvenile moult of relatively limited extent to a complete postjuvenile moult is displayed. Thus, the partial renewal of the primaries during the postjuvenile moult can be regarded as a transition or compromise between a less extensive partial and a complete postjuvenile moult. However, the usually eccentric renewal of primaries (see section 4.3.3) is a distinct characteristic of this moult strategy. In certain species which usually moult most or all of the greater coverts, tertials and rectrices, some individuals have been found to also renew some primaries. Partial primary moult has been recorded in 68% of Carduelis carduelis and in three out of seven C cannabina on the Balearic Islands (Mester & Priinte 1982), in 57% of those Sylvia melanocephala not performing a complete postjuvenile moult in Malta (Gauci & Sultana 1979), in 13% of Cyanopica cyana in S Spain (de la Cruz et al. 1992), in 10-12% of Carduelis chloris in central Europe (Westphal 1976, p. 168), in 8% of Loxia curvirostra, 4% of Carduelis cannabina and 1.1% of C. spinus in Switzerland (mostly migrants, see part II), in 3% of Sylvia atricapilla on spring migration in Italy (p. 130) and exceptionally in Motacilta alba, Carduelis carduelis, Serinus serinus and Emberiza schoenidus in Switzerland (mostly migrants, see part II). Furthermore, partial primary moult was observed in Saxicola torquata (Italy, Fracasso 1985), Sylvia conspicillata^ S. melanothorax (Roselaar in Cramp 1992, Svensson 1992), Remiz pendulinus (Greece, Kasparek 1981), Lanius excubitor (southern populations, Roselaar in Cramp & Perrins 1993), Emberiza cirlus (Italy, Winkler & Jenni 1987), probably in Certhia brachydactyla (Spain, Copete & Senar 1990) and possibly in Sylvia undata and other sedentary Mediterranean Sylvia warblers (Gauci & Sultana 1979). Most of these birds moult the primaries eccentrically, but Saxicola torquata, Carduelis spinus and C. carduelis occasionally show a descendant partial primary moult starting with PI, and Cyanopica cyana and Certhia brachydactyla an ascendant partial primary moult (see section 4.3.3). As might be expected, eccentric primary moult occurs in birds with a long potential period available for moult. They usually start breeding early in the season in central Europe (especially Carduelis spinus and Loxia curvirostra) or belong to Mediterranean populations with an earlier breeding season than in central or N Europe (see e.g. p. 171 for geographical variation in the occurrence of eccentric moult in Carduelis carduelis). In Sylvia melanocephala^ early-hatched birds perform a complete, or almost complete, postjuvenile moult, while late-hatched birds show a partial postjuvenile moult which includes a few primaries at most (Gauci & Sultana 1979). In Carduelis chloris; only the earlyhatched birds moult part of the primaries, and they prolong the usual moult duration of 50-70 days up to 95-100 days (Rymkevich 1990). Thus, partial primary moult depends on hatching date and, consequently, geographical area. It entails a longer moult duration than a partial moult without the primaries, as also shown for Carpodacus mexicanus (Michener & Michener 1940). The available data show that partial primary moult occurs in a wide variety of species. Further study, especially in the Mediterranean area,
43
will no doubt reveal it in more species and perhaps shed light on its advantages. A partial primary moult starting with P 1 and ending somewhere in the centre of the wing can be interpreted as an attempt to perform a complete primary moult which is, however, interrupted before completion. In this case, only the protected innermost primaries are renewed, and this type of partial primary moult occurs rarely. Eccentric partial primary moult differs in that a moult focus in the centre of the wing is activated only once in the life of the bird and presents a compromise between a complete primary moult and no renewal of the primaries. It renews the most exposed primaries, or those that partly cover the most exposed ones, so maximizing the effectiveness of the moult for minimum effort. An early hatching date and consequently long potential moult period are prerequisites for a partial primary moult. Furthermore, early-hatched birds would have worn the juvenile primaries for longer than late-hatched ones and, therefore, may need this reinforcement of the wing-tip before the first complete postbreeding moult. However, in some sedentary species with early hatching dates and long potential moult periods, a partial primary moult has not yet been observed (e.g. Parus spp., Sitta europaea, Troglodytes troglodytes, Cinclus cinclus, Erithacus rubecula, Turdus spp.). Reinforcement of the wing-tip may be important in birds which skulk in dense vegetation, as do some Mediterranean warblers, or which are exposed to bright sunlight (see Mester & Priinte 1982 for Carduelis spp.). Partial primary moult not only reinforces the juvenile wing, but may also change its shape and surface area (and consequently alter the wing-loading) since the newly grown primaries are usually longer than their juvenile predecessors (as shown for Vireo griseus, George 1973, and Icteria virens, Phillips 1974). Whether this results in significant benefits is not yet known. Partial primary moult has also been observed by Evans (1986) in Sturnus vulgaris, which usually perform a complete postjuvenile moult. According to this author, 45-5% of first-year birds moulted some of the primaries, some eccentrically, some apparently descendantly, but it is unclear whether this proportion also includes birds with an interrupted secondary moult (see also Williamson 1961 and Scott 1965). Most examples of partial primary moult given by Evans (1986) are from July and August, so may refer to birds which suspended moult temporarily. Partial primary moult was more frequent in island than in continental populations, but the island populations studied were also more northern in location. Furthermore, a partial primary moult was more frequent in juveniles and 2, which also moulted later, than in adults and c?. Therefore, the partial primary moult of Sturnus vulgaris could be due either to a suspension of moult for summer migration (Zwischenzug) or to the time constraints on northern and late moulting birds. Whether protein constraints, as suggested by Evans (1986), might be an additional factor remains to be shown. Interrupted primary moult (between one and seven primaries renewed) was also observed in some Passer domesticus (Harper 1984), though whether this represents a partial, a very slow or a temporarily suspended moult remains to be shown. A particular case is that of Cisticola juncidis (Fig. 35). While a complete postjuvenile moult is the normal moult strategy (Thomas 1979, Gauci & Sultana 1981), many cT from early broods may interrupt the moult for breeding activities (which can occur within a few weeks of fledging in this species; Ueda 1985). These birds renew up to six primaries descendantly, starting with P 1, as well as part of the body-feathers and wing-coverts. After interruption, the primary moult is resumed descendantly, usually from the point of interruption, but probably all of these birds moult the recently renewed inner primaries again soon after this resumption in an ascendant sequence, as well as all the other feathers (Gauci & Sultana 1981, C. Gauci in litt). Another peculiarity of the complete moult of this species is that at least 74% of juveniles and adults renew the central tertial (and occasionally others) and at least 55% renew up to five greater coverts (occasionally all) a second time at the end of the primary moult (Gauci & Sultana 1981).
44
The Moult During the First Year of Life
Fig. 35. Cisticolajuncidis ly, 23 November. P 1+3-4 postjuv, 2+5-10 juv (on the other wing P 5 growing). S 1 almost full-grown postjuv, 2-5 juv, 6 in pin and hidden. T, GC, CC, MaC and MeC postjuv. Al 1 postjuv, 2-3 growing postjuv. PC juv. P 1 is slightly older than primaries 3-4. Thus, this bird probably interrupted primary moult after renewing P 1, resumed it later with P 3 and is now moulting slowly and including the secondaries in a convergent sequence, typical of this species (cf. section 3.2.3).
4.5 Complete postjuvenile moult in the breeding area Only a few European passerines regularly perform a complete postjuvenile moult in the late summer/autumn (species see Table 5, p. 53). In Sylvia melanocephala part of the population do so (Gauci & Sultana 1979, Vowles & Vowles 1987) and in Loxia curvirostra and Carduelis Moris a few individuals do (see part II). Complete postjuvenile moult may perhaps be observed in some individuals of other species (see e.g. Carduelis spinus and C. carduelis in part II; Sylvia conspicillata, Gauci & Sultana 1981; S. melanothorax, Roselaar in Cramp 1992). These complete postjuvenile moults follow the basic sequence described in chapter 3.2. Whether or not the complete moult of some first-year long-distance migrants, during winter in Africa, actually represents a true complete postjuvenile moult is discussed in section 4.6.2. Here, only species performing their complete postjuvenile moult in late summer/ autumn, in the breeding area, are discussed (moult cycles 1 and 2 in Table 3). Most species start the complete postjuvenile moult when one to two months old (Alaudidae, Glutz & Bauer 1985; Panurus biarmicus, Pearson 1975B; Passer spp., Heinroth & Heinroth 1926, Deckert 1962; Montfringilla nivalis, Winkler &: Winkler 1985; Sturnus vulgaris, Lundberg & Eriksson 1984, Rymkevich 1990). Cisticola juncidis starts this moult later at two to three months of age (Gauci & Sultana 1981) and Acrocephalus melanopogon later still, from two to four and a half months of age (Leisler 1972). Thus, the juvenile primaries are usually only worn for several weeks after fledging. For instance in Montifringilla nivalis, P 1 is shed as soon as 12 days after the juvenile P 9 is full-grown (Winkler & Winkler 1985). Compared with the postbreeding moult of adults, the postjuvenile moult is less synchronized within a population, especially in multibrooded species (e.g. Bahrmann 1964, Alonso 1984, Peris 1988), and may start slightly later than in adults (e.g. Miliaria calandra, Gauci & Sultana 1983; Passer montanus, Aegithalos caudatus, Ginn & Melville 1983; Sturnus vulgaris, Bahrmann 1964; S. unicolor, Peris 1988). The complete postjuvenile moult is usually roughly similar in duration to that of the postbreeding moult of adults, or slighdy longer, especially in early-hatched young (Passer montanus Deckert 1962; P. domesticus, Zeidler 1966; 2 Cisticola juncidis, Gauci & Sultana 1981, $ see p, 25), although it is shorter in Sylvia melanocephala (Gauci &
Sultana 1979). It usually lasts from about 60â&#x20AC;&#x201D;80 days (Alauda arvensis, Ginn & Melville 1983, Glutz & Bauer 1985; Eremophila alpestris, Glutz & Bauer 1985; Cisticola juncidis, Sylvia melanocephala, Gauci &: Sultana 1979, 1981; Miliaria calandra, Gauci & Sultana 1983, Ginn & Melville 1983; Passer domesticus, Zeidler 1966, Ginn & Melville 1983, Alonso 1984; P. montanus, Ginn & Melville 1983; P. hispaniolensis, Alonso 1984). A shorter duration is reported only in Panurus biarmicus (42-56 days depending on hatching date, Spitzer 1972, Buker et ai 1975, Pearson 1975b), Acrocephalus melanopogon (47.5 days, Leisler 1972) and late-hatched (50 days, Zeidler 1966) and Finnish (52-64 days, Dyer et al. 1977) Passer domesticus. Sturnus vulgaris takes about 80 days for its primary moult (Ginn & Melville 1983), but the total moult duration of captive birds is reported to range from 87-130 days (Lundberg & Eriksson 1984, Rymkevich 1990). Aegitalos caudatus takes 75-100 days to moult (Ginn & Melville 1983), while Montifringilla nivalis has an exceptionally long moult duration of 108 days (93 days for the primaries), at least in captivity, which sets the end of postjuvenile moult as late as midNovember to early December (Winkler & Winkler 1985). This might be an adaptation to its harsh mountain environment. As with the partial postjuvenile moult, late-hatched birds perform a complete postjuvenile moult at an earlier age and more rapidly than early-hatched birds (Acrocephalus melanopogon, Leisler 1972; Panurus biarmicus, Pearson 1975b; Cisticola juncidis, Gauci & Sultana 1981; Passer domesticus, Zeidler 1966; P. montanus, Deckert 1962, Myrcha & Pinowski 1970, Sutter 1985; P. hispaniolensis, Alonso 1984; Sturnus vulgaris, Rymkevich 1990). Similarly, Finnish Passer domesticus moult more quickly than more southerly populations (Zeidler 1966, Dyer et ai 1977, Ginn & Melville 1983, Alonso 1984). In Sturnus vulgaris held under constant daylength, birds from a sedentary N Norwegian population started to moult at a similar age, but more rapidly than birds from a migratory Swedish population, suggesting an endogenous difference in moult duration (Lundberg & Eriksson 1984). Why some species should perform a complete postjuvenile moult has hardly been studied and remains obscure. The presence of a complete posrjuvenile moult appears to stem from phylogenetic relationships. It is remarkable that all European members of the Alaudidae, Passeridae, Sturnidae, Timaliidae, Aegithalidae and the genus Cisticola perform a complete postjuvenile moult: they are all predominantly tropical taxa whose rropical representatives also normally perform a complete postjuvenile moult. A long period available for moult is certainly a prerequisite for this particular habit. However, the age at which this moult commences (30-60 days) is basically similar to that of short-distance migrants and sedentary species which perform a partial postjuvenile moult, and its duration (60-80 days) is only about two weeks longer (cf. Fig. 33). Another prerequisite supposes a rich and easily accessible food supply which provides sufficient energy and nutrients and can be utilized despite a reduction of flight capability during the first months of independence. However, it remains unclear whether or not species performing a complete postjuvenile moult do in fact generally have access to richer and more accessible food resources than species performing a partial moult. In P. biarmicus and A. melanopogon, limited flight requirements in their dense marshy habitat may facilitate their particularly rapid complete postjuvenile moult (Pearson 1975b). CJ. Mead (in Ginn & Melville 1983) pointed out that the nestlings of many species moulting the juvenile plumage completely are reared on vegetable food and proposed that such a diet might be deficient in certain amino acids, causing the juvenile feathers to be less durable. However, the majority of species with a complete postjuvenile moult actually feed their nestlings largely on arthropods. Furthermore, it has still not been shown whether the juvenile remiges are really less durable than those of adults and whether the remiges of species with a complete postjuvenile moult are less durable than those of species moulting partially (cf. Fogden 1972 for tropical species).
Moults during the first year of Life in trans-saharan migrants
4.6 Moults during the first year of life in trans-saharan migrants The moult cycles during the first year of life of all sedentary species and short-distance migrants (all of which moult as adults according to moult strategy 1 or 2, see Tables 1 and 2) are rather uniform and well known (moult cycles 1-6 in Table 3, sections 4.4 and 4.5). Long-distance migrants, whose adults perform a complete postbreeding moult before autumn migration, also follow moult cycle 5 or 6 (Table 3). As with the moult strategies of adults, the moult cycles during the first year of life of long-distance migrants, whose adults perform a complete moult in the tropics or a seasonally divided moult, are more complex and also far less well known than those of sedentary species and short-distance migrants. The information on their moult cycles is scarce since birds in their first year of life have only rarely been distinguished from adults and many published reports cannot be assigned to age groups and have had to be omitted from both the account of the moult strategies of adults and this section. As with the adults, we therefore concentrate on those European passerines wintering in Africa in the remainder of this section.
4.6.1 Partialpostjuvenile and partial prebreeding moult excluding remiges: Moult cycles 5 and 6 All species which perform a partial prebreeding moult as adults after the complete postbreeding moult in the breeding area (moult strategy 2 in Table 1) also show a partial prebreeding moult which follows the partial postjuvenile moult (moult cycle 6 in Table 3). Until now, there has been little information as to whether the timing, duration and extent of the prebreeding moult during the first winter is similar to that of adults. In all species examined, we found that second-year birds perform a more extensive prebreeding moult than adults (Anthus trivialis, A. spinoletta, Motacilla flava, M. alba, Saxicola rubetra, Sylvia c. communis, Emberiza hortulana, details see part II), similar to the case in two American species (Cannell et al. 1983, Greenwood et al. 1983). Ficedula hypoleuca moults similar numbers of greater coverts and tertials during the first winter, but significantly more secondaries than during later winters (p. 142). Long-distance migrants without a prebreeding moult, or with one of very limited extent, perform a postjuvenile moult which includes at least all the body-feathers, marginal and median coverts, usually part of the greater coverts and occasionally some tertials (e.g. Luscinia spp., Phoenicurus phoenicurus, Oenanthe pleschanka, O. hispanica). In contrast, long-distance migrants with a considerable prebreeding moult perform a postjuvenile moult in the breeding area of limited extent, during which part of the juvenile body-feathers may even be retained (see p. 39). In these species, the rest of the juvenile bodyfeathers and at least part of the juvenile wing-coverts are replaced during the partial prebreeding moult during the first winter, which is considerably more extensive than the postjuvenile moult (e.g. Ficedula hypoleuca, Anthus trivialis). Thus, the partial prebreeding moult during the first winter might have the additional purpose of making up a postjuvenile moult of very limited extent before autumn migration and, therefore, might be more extensive than in the adults.
4.6.2 Complete moult in the non-breeding area: Moult cycles 9, 10, 11, 14 and 15 Species which show a complete moult in Africa as adults (moult strategy 3, 5 and 6 in Tables 1 and 2) usually also moult completely during their first winter (moult cycles 9, 14 and 15 in Table 3). So far, the only known exceptions are Lanius s. senator, some L L isabellinus and L. minor and possibly, rarely L, collurio, as well as those species in
45
which some of the adults also do not moult completely (see section 4.6.3). Furthermore, two species (Carpodacus erythrinus, Emberiza a. aureola) wintering in tropical Asia apparently perform only a partial moult during their first winter, but show a complete moult as adults (Stresemann & Stresemann 1969a, Bozhko 1980; moult cycle 10 and 11 in Table 3). In C. erythrinus, this partial moult includes the bodyfeathers, wing-coverts, tertials, rectrices and occasionally the outer primaries, and is only rarely complete (Bozhko 1980), In both C. erythrinus and E. a. aureola, the adults and first-year birds do not moult before the onset of autumn migration, while E. a. ornata does so (Stresemann & Stresemann 1969a, Rymkevich 1983, 1990, Strom 1991). Thus, in C erythrinus and E. a. aureola the postbreeding and postjuvenile moult seem to be delayed until the arrival in the first staging area in late autumn. Additionally, E. aureola shows a partial prebreeding moult restricted to the feathers of the head, before spring migration (moult cycle 11 in Table 3). The moult preceding the autumn migration of first-year birds which perform a complete moult in Africa, is of limited extent or may be completely suppressed (e.g. Acrocephalus palustris according to Dowsett-Lemaire 1981; A. schoenobaenus, Griill & Zwicker 1982; A. paludicola, Roselaar in Cramp 1992; Locustella luscinioides, Miiller 1981). It usually includes only apart of the body-feathers, marginal and median coverts and, rarely, some greater coverts, at most all of the bodyfeathers, marginal and median coverts as well as the innermost greater coverts (e.g. Sylvia borin). As in adults, it is not clear whether this very restricted premigratory moult is actually a postjuvenile moult in its own right, or the beginning of the complete postjuvenile moult which takes place mainly in Africa. First-year Hirundo rustica, Delichon urbica and Riparia riparia perform the complete moult only in Africa, but may start to renew the juvenile body-feathers (and rarely some primaries, not shown in Table 3) before autumn migration. The current interpretation is that the complete moult of first-year birds in Africa is actually the postjuvenile moult which may already start before autumn migration (Glutz & Bauer 1985, Roselaar in Cramp 1988, part II). This agrees with the view that the postbreeding moult of the adults is delayed until winter. An additional, prebreeding moult of both age classes was found in Delichon urbica (Broekhuysen 1953) and possibly Riparia riparia (Pearson 1971). The same interpretation may apply to some of the Acrocephalus, Locustella and Hippolais warblers and to Anthus campestris (cf. Roselaar in Cramp 1988, 1992) as well as to certain long-distance migrants wintering in tropical Asia (e.g. Carpodacus erythrinus, Emberiza a. aureola, E. bruniceps, E. melanocephala-, Stresemann & Stresemann 1969a, Rymkevich 1983, 1990) which either perform a very restricted moult or no moult at all before autumn migration. However, in other species moulting more extensively before the autumn migration, the feathers renewed in autumn are very probably renewed again during the complete moult in Africa (e.g. Sylvia borin) so that the premigratory moult may represent the actual postjuvenile moult. As discussed earlier (sections 3.3.3 and 3.4.2), adults which moult completely in winter may suspend the moult in Africa and show an additional partial moult before spring migration. Since first winter birds have rarely been recorded separately from adults, it remains to be seen whether the two age classes differ in their moult cycles while in Africa (see e.g. Pearson 1973 for a possible age related difference in Acrocephalus scirpaceus), In species whose adults show an extensive partial or complete moult in the breeding area, or in NE Africa, before a complete moult further south (moult strategy 5 or 6 in Tables 1 and 2), first-year birds perform either a postjuvenile moult of only limited extent, or hardly any moult at all, before autumn migration. Adult Acrocephalus palustris moult the body-feathers in NE Africa before the complete moult in southern Africa, while first-year birds do not show this body-feather moult, but renew their plumage for the first time in southern Africa (Pearson & Backhurst 1976, Pearson 1982, 1989). Similarly, adult Locustellafluviatilis moult the body-feathers and outer primaries in NE Africa during
46
The Moult During the First Year of Life
the autumn (moult strategy 5 in Table 2), while first-year birds do not (Pearson & Backhurst 1983; moult cycle 14 in Table 3). The postjuvenile moult of Sylvia borin, whose adults may occasionally moult almost completely in the breeding area (moult strategy 5 in Table 2), is always of limited extent. Phylloscopus trochilus, Lanius tigrinus and L. cristatus, which perform (almost) two complete moults annually as adults (moult strategy 6 in Table 1), moult only the body-feathers in their first summer/autumn (p. 136, Stresemann & Stresemann 1971; moult cycle 15 in Table 3). First-year birds of some species exhibit the complete moult in Africa later than the adults (e.g. Hirundo rustica in Zambia and Zaire, but not in southern Africa, Herroelen 1960, de Bont 1962, Broekhuysen & Brown 1963, Francis 1980; Acrocephalus schoenobaenus, Bensch et ai 1991; Sylvia borin and possibly A scirpaceus, Pearson 1973; Lanius collurw, B. Bruderer pers. comm.). This earlier moult of adults might be related to their earlier autumn migration, possibly helped by the absence of a complete premigratory postbreeding moult. However, both first-year and adult Phylloscopus trochilus moult at the same time (Pearson 1973), coinciding with a complete postbreeding moult in adults, and also show similar timing of the autumn migration.
4.6.3 Partial moult including remiges in the non-breeding area: Moult cycles 7> 8y 12 and 13
24% of Sylvia c. communis replace pan, rarely all, of the primaries during their first winter, usually eccentrically (moult cycle 8 in Table 3; probably similar in Lanius nubicus, Roselaar in Cramp & Perrins 1993). Thus, the replacement of the outer primaries especially, during the first winter could also be interpreted as a preparation for a possible primary moult interruption during the following postbreeding moult. In Sylvia c. communis, the peculiar primary moult pattern of some birds during the postbreeding moult (see p. 123) may actually be complementary to an eccentric first prebreeding moult (see section 3.3.3). However, an eccentric renewal of primaries in the first winter was also found in Sylvia nisoria (Hasselquist etaL 1988, Lindstrom et al. 1993), S. cantillans (Roselaar in Cramp 1992, own data; Fig. 31) and S. hortensis (Williamson 1968, Roselaar in Cramp 1992), all species in which primary moult suspension in adults is exceptional, or absent (except in captive S. hortensis). Therefore, many individuals of these Sylvia species probably renew some of the primaries twice during the first year of life, i.e. during an extensive first prebreeding and during the first postbreeding moult. As discussed in the preceding section on secondary moult, it remains unclear whether or not a partial primary moult during the winter is part of a continuation of the postjuvenile moult (cf. Roselaar in Cramp 1988, 1992, Cramp & Perrins 1993) and whether it is temporally separated from the actual prebreeding moult.
First partial prebreeding moult including secondaries
Incomplete first prebreeding moult
All species which may renew the secondaries during a partial prebreeding moult as adults (group 3 and 4 in Table 2) may also do so during their first winter (Sylvia nisoria^ Hasselquist et al. 1988, Lindstrom et al. 1993; S. cantillans, own data; S. communis, S. curruca, Ficedula hypoleuca see part II; S. hortensis, Williamson 1968, Berthold &: Querner 1982a; probably Lanius nubicus, Roselaar in Cramp & Perrins 1993; moult cycle 7 in Table 3). First winter Ficedula hypoleuca renew the secondaries even more frequently than do the adults (p. 142). As discussed in section 3.3.3, the first winter renewal of the secondaries in these species may be interpreted as a preparation for a possible retention of secondaries during the subsequent postbreeding moult. Additionally, it may also provide a more adult-like plumage, especially in cT F. hypoleuca. The renewal of the secondaries occurs during an extensive prebreeding moult which includes the body-feathers, most wing-coverts, the tertials and often the rectrices. As observed in actively moulting S. nisoria in Kenya, the secondaries are usually moulted convergently, though irregular sequences occur as well (A. Lindstrom pers. comm.). First winter S. c. communis and F. hypoleuca appear to generally moult the secondaries descendantly (see part II). Replacement of some secondaries during the first winter also occurs in individual Anthus campestris which suspend the postbreeding moult as adults (p. 66). Emberiza hortulana may be an exception to this moult cycle (and is not shown in Table 3), since the second-year spring birds examined had not renewed any secondaries (p. 195). Thus, this species might retain the juvenile secondaries, which are often not moulted during the postbreeding moult, for one and a half or two years. Second-year spring birds of Sylvia nisoria, S, cantillans, S. communis and S. curruca often show differently worn non-juvenile wing-coverts within the same wing (own obs., see part II). It is not yet clear whether they have been moulted at different times during a protracted prebreeding moult or whether there is an additional, possibly overlapping, moult (cf. section 3.3.3). In the latter case, the first 'prebreeding' moult in Africa might be interpreted as a continuation of the postjuvenile moult (cf. Roselaar in Cramp 1992).
The strategy of some adults whereby some secondaries are retained during an otherwise complete prebreeding moult before renewing some secondaries during the partial postbreeding moult (group 6 in Table 2) is also followed during the first year of life by an even higher percentage of Oriolus oriolus (p. 153; moult cycle 12). Because the ages of individual Muscicapa striata observed in the non-breeding area were not determined, it remains to be shown whether or not both age classes of this species follow the same moult cycle. Whether the secondary moult is resumed at the point of interruption during the postbreeding moult is not known (cf. p. 139) and the reasons for this particular moult strategy remain unclear. In certain long-distance migrants of the Laniidae, the reduction of the first prebreeding moult may involve some primaries as well as some secondaries, while adults perform a complete prebreeding moult. This is the common strategy of Lanius senator senator and L s. badius. Firstyear birds show a postjuvenile moult of limited extent in the breeding area. During the winter, they do not moult completely (cf. Lanius collurw), but retain up to five of the innermost primaries (Fig. 32), none to six of the secondaries (see also section 4.3.3), none to all primary coverts and rarely some alula feathers (Ullrich 1974, Svensson 1992, Roselaar in Cramp & Perrins 1993, own data; Fig. 36). The rest of the plumage is renewed. However, among 53 second-year spring birds, three renewed all the primaries (one of them also replaced all the secondaries, and PC 7 and 8 were the only juvenile feathers retained, own data, Fig. 37). Thus, a complete moult during the first winter possibly occurs as well. During the first postbreeding moult, secondyear birds often start to renew the juvenile innermost primaries as well as the juvenile primary coverts while still in the breeding area. They may then show three generations of primaries simultaneously, e.g. P 2 juvenile, P 3-10 prebreeding, P 1 postbreeding (Ullrich 1974, Svensson 1992). Primary moult is probably then suspended until arrival in the African winter quarters (moult cycle 13 in Table 3). In contrast to all other European passerines, this species takes two years to enter the adult moult cycle with its partial postbreeding moult before the autumn migration and subsequent complete moult in Africa (moult strategy 3 in Tables 1 and 2). Similarly, some first winter Lanius i. isabellinus may also probably retain the innermost primaries during the first prebreeding moult (Stresemann & Stresemann 1972a). However, the peculiar start of
First partial prebreeding moult including primaries Among the two species which regularly suspend primary moult as adults, Anthus campestris may renew the central primaries (p. 66) and
Moults during the first year of life in trans-saharan migrants
47
4.6.4 Conclusions
Fig. 36. Lanius senator badius 2y 9 after partial prebreeding moult, 22 April. Unlike the adults, most first winter Lanius s. senator and L s. badius do not perform a complete moult in Africa, but retain primaries, secondaries, primary coverts and rarely alula feathers. This bird retained primaries 1â&#x20AC;&#x201D;3, secondaries 1â&#x20AC;&#x201D;5, all primary coverts and alula 2,
Fig. 37. Lanius senator senator 2y <S after almost complete prebreeding moult, 5 May. Rarely, first winter L. s. senator and L. s. badius moult all remiges in Africa. This bird can be recognized as 2y only by the retained primary coverts 7-8. primary moult in the breeding area during the first postbreeding moult, shown by Lanius senator> has not been observed in these species (which is not included in Table 3). In Lanius cristatus, which usually shows two complete moults each year, the subspecies lucionemis generally retains the innermost primaries during the prebreeding moult, although it is not clear whether this occurs only in first winter birds (Stresemann & Stresemann 1971). Among 15 captive Lanius collurio, two birds only renewed the four or five outermost primaries during their first prebreeding moult (Gwinner & Biebach 1977). Thus, in the Laniidae incomplete primary moult during the first year of life appears to be a regular phenomenon, especially in the non-breeding area (but see Miller 1928 for Z, ludovicianus in the breeding area). However, only Lanius senator appears to start and then suspend the next primary moult during the first postbreeding moult. The partial moult of the remiges in the Laniidae may serve to shorten the total moult duration in first winter birds which (at least in Lanius isabellinus and L. collurio, Stresemann & Stresemann 1972a, B. Bruderer pers. comm.) starts later than in adults. However, Bensch et aL (1991) mention that first winter Lanius senator moult more slowly, thus might better maintain their capacity for flight during their first stay in Africa than the adults. First-year Locustella luscinioides often renew only the outer or central primaries during the winter (Roseiaar in Cramp 1992). How this relates to the complex and variable moult strategy of the adults of this species remains to be shown.
The moult cycles of trans-saharan migrants during their first year are, like the adult cycles, poorly understood. For instance, it is often not clear whether the restricted postjuvenile moult that precedes autumn migration represents the beginning of the complete moult performed mainly in Africa or whether it is a postjuvenile moult in its own right (consequently, moult cycle 9 in Table 3 may actually consist of a variety of moult cycles). This problem confuses the classification and nomenclature of plumage and moult cycles between species, one of the earliest aims of the study of moult. In particular, we can still not be certain whether the first moult after hatching, designated the postjuvenile moult, is homologous among all species, although it may have this connotation for some readers. It must be reiterated that the terms given to plumages and moults in this book do not indicate homologies, but that they merely refer to the occurrence of moult relative to the breeding season and autumn migration in a strongly seasonal environment (see section 2.2.1). The moult of migrants in Africa requires further study and the collection of separate data for adults and first-year birds. The moult of first-year birds in Africa might, in some species, actually consist of two (overlapping?) moults, similar to that of adults (see section 3.3.5; Motacilla flava and Anthus cervinus, Pearson & Backhurst 1973, D.J. Pearson in //'#.; possibly Sylvia communis> S. cantillans, S. nisoria, see section 4.6.3). There may thus be three moult phases during the first year in certain species (see Rohwer 1986, Thompson 1991 and Young 1991 for American Passerina species). In summary, most trans-saharan migrants enter the moult cycle of the adults during their first winter. Exceptions are some Laniidae with a reduced first prebreeding moult, Locustella fluviatilis and Acrocephaluspalustris which omit the partial moult in NE Africa in the first autumn, and some species which perform a more extensive first prebreeding moult than the adults (e.g. some Sylvia warblers). Furthermore, Carpodacus erythrinus and Emberiza a. aureola show only a partial moult in their first winter, not a complete moult as do the adults. There appears to be a relationship between the extent of the moult before autumn migration and the extent of the first moult in Africa. Species with a restricted premigratory moult are more likely to show an extensive or complete first prebreeding moult. The retention of remiges during the first postbreeding moult, due to a seasonally divided moult, in first-year birds seems to result from their moulting these feathers half a year in advance, during an extensive first prebreeding moult. However, it is still not known whether this is always the case or whether some birds may retain some juvenile remiges for one and a half or two years (probably some secondaries in Emberiza hortulana and in some Sylvia communis and S. nisoria\ possibly secondaries and primaries in Anthus campestris\ some primaries in Lanius senator]. There seem to be four types of partial moult of remiges during the first winter, which are related to the moult strategies of the adults. (1) Birds which renew some secondaries during an extensive partial prebreeding moult (moult cycle 7), probably as a preparation for a possible retention of some secondaries during the subsequent postbreeding moult. (2) Birds which retain some secondaries during an otherwise complete first prebreeding moult and usually replace them during the subsequent postbreeding moult (moult cycle 12), as do some of the adults. The reasons for this moult cycle remain obscure. (3) Birds which renew part of the primaries during an extensive first partial prebreeding moult (moult cycle 8) perhaps to prepare for a subsequent primary moult suspension, but which may renew primaries for other reasons also. (4) Certain long-distance migrant Laniidae which reduce the complete prebreeding moult during their first winter to a partial moult, possibly to shorten the moult duration, or to reduce wing raggedness during moult, while the adults generally perform a complete moult.
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PART II CHAPTER 5
Ageing European Passerines 5.1 Ageing criteria in live birds The most common aim of ageing is to assign individual birds to age classes based on years. In passerines, birds in their first year of life are to be distinguished from older (adult) birds (normally the terminology referring to the calender year is applied, see section 2.3). Older age classes can only be distinguished in a few European passerine species. During the first months of life, the age of a bird may be estimated more precisely (in days) using the progress of plumage developement and postjuvenile moult (see section 4.3) or of skull pneumatization (see section 4.4.3), techniques which will not be discussed further here. In part II of this book, ageing refers to the distinction of birds during their first year of life from older birds. Although any character which changes with age can be used as an ageing criteria, for live birds examined in the field, such criterion are limited to external features which can be examined by eye, such as plumage characters (see sections 5.2 and 5.3), skull pneumatization (see appendix) and the appearance of bare parts. Each potential ageing criterion must be tested for reliability by some independent means of ageing. The use of ringed birds of known age as a reference is infallible, but limited to retraps, which are not usually numerous. In summer/autumn, skull pneumatization is among the most important independent ageing criteria applicable to the majority of birds (see appendix). The reliability of any ageing criterion depends partly on the way the character changes with age. Many bare parts change gradually with increasing age, such as the colour of the iris (e.g. Kuschert 1980, Karlsson et al. 1985, 1988, Leverton 1987, Shirihai 1988, Gargallo 1992), orbital ring (Gargallo 1992), eye-lid (Reichholf-Riehm 1977), inside of the upper mandible (e.g. Hogstad 1971, Karlsson et al. 1986a,b, 1988), tongue (e.g. in Sturnus vulgaris, Svensson 1992), bill (e.g. in Ptyonoprogne rupestris, Svensson 1992), tarsus and feet (e.g. Karlsson et al 1988) as well as the shape of the bill (e.g. Bub 1985, Svensson 1992). Such characters are most useful for separating firstand second-year birds from adults when the colour change occurs not too soon after fledging, but before the first breeding season. Inevitably, there is a certain transitional range within a character during which a bird cannot be reliably attributed to either of the two age classes. This is accentuated by individual variation in hatching date and the speed of the colour change. Thus, characters which change gradually with age must be examined for ease of recognition, reliability and consistency among individuals. In certain species, the age classes may be easily separated at a certain season (e.g. Leverton 1987, Karlsson et aL 1988, Gargallo 1992, p. 101), while at other seasons, some of the individuals are impossible to age or are assigned to the wrong age class (e.g. Kuschert 1980, Pettersson 1983, Karlsson etal. 1986a,b, 1988, see also p. 89). In some species, the age difference in the colour of the bare parts is confounded by differences between the sexes (e.g. iris colour, Buxton 1947, Neuschulz 1988) or seasons (e.g. bill colour in Turdus merula, Miles 1971, Glutz & Bauer 1988). In the case of skull pneumatization (see appendix) and tongue spots (in the genera Cettia, Locustella, Acrocephalus, Hippolais\ Kuschert 1980, Karlsson et aL 1988, Svensson 1992), a character typical of young birds disappears with time. Again, these characters are most useful when the change does not occur too soon after fledging, but before the first
breeding season. Usually, such characters are easy to recognize. Provided that all individuals lose the juvenile character (i.e. non-pneumatized skull windows, tongue spots), young birds can be recognized with certainty. Adults, however, can only be determined before the time when the first juveniles attain the adult state. Thus, it is vital to know whether some adults may retain the juvenile state as well as when and how synchronized is the disappearance of the juvenile character from young individuals. Tongue spots may be present in some adults (e.g. Kuschert 1980, Karlsson et aL 1988) and a few species regularly retain non-pneumatized skull windows as adults (see appendix). Most plumage characters indicative of age concern differences between juvenile feathers and those of subsequent feather generations. Such characters change suddenly when these feathers are moulted and there can thus be no doubt about a bird's age, provided that all individuals moult in the same way and at a similar, known, age. Such plumage characters must be checked for ease of recognition and for time, constancy and synchronization of the change among individuals. Other plumage features vary continuously (e.g. wing-length, relative or absolute length of certain feathers, shape of rectrices, shape and structure of primary coverts) and individual variation produces a smaller or larger overlap in the distributions of the character between the age classes. In most species, linear measurements, especially the length of feathers or the wing, show too much overlap between the two age classes to be a useful criterion (e.g. Alatalo et aL 1984, Winkel & Winkel 1992, but see Nakamura 1990). On the other hand, the length of primary 10 relative to the primary coverts is a very useful ageing character in Panurus biarmicus. The shape of the rectrices and primary coverts may be a helpful character in certain species (e.g. Laaksonen & Lehikoinen 1976, Amann 1980, Pettersson 1983, Karlsson et aL 1986a), while in others it assigns many individuals to the wrong age class (e.g. Sylvia atricapilla own obs.; Regulus spp., Jackson 1992, own obs.) (see also Svensson 1992). In many species, there is no easily recognizable ageing criterion applicable to all individuals. In such cases, we do not recommend the use of single characters or dichotomous ageing keys, but strongly advise the examination of several characters on the same bird. If any one of the presence-absence characters can be assessed with certainty, it should be given preference over the other characters. Consequently, we stress the recognition of juvenile feathers and skull pneumatization as ageing criteria in the species accounts and give indications regarding the ease of recognition and constancy of these characters.
5.2 Ageing using plumage characters Ageing by plumage characters is based on the recognition of juvenile feathers and/or on recognizing differences in the extent of moult. In both cases, a thorough knowledge of the moult cycles and of the variation in the extents of moults is a prerequisite. In a few species, differences between postjuvenile and adult feathers exist.
5.2.1 Recognition of juvenile feathers In most European passerines, the juvenile feathers differ in structure and often also in coloration from subsequent feather generations. The
50
Ageing European Passerines
feathers which replace the juvenile plumage, however, are generally adult-like in colour and structure (see section 4.2). Thus, all juvenile plumage features are generally lost when the last juvenile feather has been moulted. Intermediate 'immature' plumages acquired during moults in the first year of life are exceptional or differ only slightly from the adult plumage (see section 5.2.3), in contrast to many large nonpasserines.
Structure and shape In most species, the juvenile body-feathers are more loosely textured, especially those of the neck, mantle and tail-coverts (see section 4.1, Fig. 24â&#x20AC;&#x201D;26). In a very few species only, the juvenile body-feathers are indistinguishable from the adult in texture (e.g. hirundines). With the exception of a few species, first-year birds replace all their body-feathers during the postjuvenile moult. The difference in texture between retained juvenile and adult wing-coverts, rectrices and remiges, however, is, if any, slight and difficult to recognize. The juvenile primary coverts, rectrices and remiges are often narrower and more pointed than the corresponding feathers of subsequent generations. This may be a useful ageing criterion in some species (e.g. Paruspalustris, /*. montanus, P. cristatus\ Laaksonen & Lehikoinen 1976, Amann 1980), but in many, there is considerable overlap in shape between juvenile and adult feathers. If two feather generations are present within the same feather tract, they may differ in shape and length, which facilitates the recognition of moult limits. In certain species, there are conspicuous differences in shape and length between juvenile and postjuvenile/postbreeding primary 10 (e.g. Panurus biarmicus, Pica pica)) central primaries (Coccothraustes coccothraustes) and rectrices (Hirundo rustica, Aegithalos caudatus).
Coloration In species which exhibit conspicuous colour differences between the juvenile and subsequent plumages (e.g. Erithacus rubecula}^ birds in the juvenile plumage and first-year birds which retain some juvenile bodyfeathers after the postjuvenile moult are easily recognized (e.g. juvenile body-feathers in Anthus campestris, retained juvenile uppertail-coverts in Muscicapa striata, Ficedula hypoleuca). In many species, colour differences between the wing-coverts, rectrices and remiges of the juvenile and subsequent feather generations are important ageing criteria. In many cases, however, these differences are slight or virtually nonexistent, but may be affected by wear which often intensifies them. In good light, differences in the colour intensity, brilliance or gloss of the feather centres, as well as in the colour and colour pattern of the fringes can be detected and are important characters for recognizing juvenile feathers and moult limits. Many examples are given in the species accounts. In a few species, the colour pattern of the juvenile flight feathers is different from that of the adults (e.g. tertials of Ficedula hypoleuca^ outer primaries of Bombycilla garrulus, primary 9 of Pica pica, central primaries in Coccothraustes coccothraustes', outer rectrices in some Sylvia warblers).
Wear The juvenile feathers grow at a time when the adults have usually worn their feathers for between half and almost a full year. Thus at fledging, the juvenile feathers are fresh (with the exception of some possible wear whilst in the nest), while those of the adults are usually worn. This difference in wear is often a useful ageing criterion in summer in species in which the juvenile plumage is similar in coloration to that of the adults (e.g. Acrocephalus scirpaceus) and in species with a complete postjuvenile moult, provided that some outer primaries are not yet moulted. In most species which moult completely in winter, this differ-
ence in wear is an important ageing criterion until the next complete moult (see section 5.3.4). As the feather fringes wear off, the colour pattern of certain feathers may change with time. In most species, the adults renew their plumage soon after the breeding season. Consequently, there is only a difference of up to several weeks in wear between juvenile and postbreeding feathers after the summer/autumn moult period. However, since the juvenile feathers are less durable and since they are slightly older than those of the adults, a difference in wear may still be obvious and becomes progressively more pronounced. The precise degree of feather wear depends on the species, individual and exposure of the particular feather (see section 1.2.1). Thus, recognizing feather generations by their degree of wear requires a lot of experience, unless two feather generations can be compared within the same feather tract. The utility of recording the extent of wear in moult studies is discussed in Rogers (1990) who provides a classification of feather wear.
Growth bars and fault bars Feathers grow day and night at a similar rate (Murphy & King 1986). During the night, when most birds are fasting, the feather material deposited is of slightly different quality than during the day. This results in a pattern of alternating day-night growth bars on the vane which is not normally visible on casual inspection, but may be seen in reflecting light in some species and feathers, especially the rectrices and remiges (Michener & Michener 1938, Wood 1950, Stiefel in Bub 1985, Winkler et al, 1988). Under certain circumstances, feather growth is disturbed resulting in more severe alterations in structure and pigmentation and, consequently, more or less conspicuous growth bars of different width and/or of structurally inferior quality (e.g. Stiefel in Bub 1985, Murphy et ai 1989; Fig. 38-41). If such disturbance of feather growth is severe, the resulting low-quality bars are called fault bars. If visible, irregularities in growth bars are equal on all feathers grown simultaneously (Michener & Michener 1938; Fig. 38â&#x20AC;&#x201D;40). However, the conspicuousness of irregularities in growth bars often varies among simultaneously grown feathers, and can even be absent on some. The reasons for variations and irregularities in growth bars are still in dispute. Some authors believe that fault bars are due to nutritional stress (summarized in Machmer et al. 1992), but others have shown that they may be caused by stress situations such as handling, perhaps amplified by malnutrition (King & Murphy 1984, Murphy etaL 1988, 1989, Machmer et al. 1992). The widths of the regular growth bars certainly reflect the growth rates of the feathers and may be influenced by nutrition (e.g. Michener & Michener 1938, Grubb 1989). If the same pattern of irregularities in growth bars is present on several feathers of the same or adjacent feather tracts, the relative timing of growth of these feathers can be assessed. In some cases, conclusions about the bird's age may be drawn, but such conclusions need to be drawn with care. Since the feather-tip grows first and more material added at the base, feathers grown at the same time show fault bars at approximately the same distance from the tip. This is the case in juvenile feathers which are grown simultaneously in the nest (Fig. 38â&#x20AC;&#x201D;39). If the feathers are grown sequentially within a tract, the fault bar pattern shows progressively further away from the feather-tip and, depending on the shedding intervals, may be present on only a few feathers (Fig. 40). This is the pattern produced by a sequential moult, typical of adults in many species. An instructive example is the blue and black barring on the wing of Garrulus glandarius which seems to represent growth bars and whose pattern of irregularities is a good ageing criterion (see p. 156). However, great care is needed when applying this technique (cf. Svensson 1992). Growth bar patterns may differ in conspicuousness
Ageing using plumage characters
51
Fig. 38. Sylvia curruca ly after partial postjuv moult, 25 August. Fault bars are present across all primaries and secondaries at similar distances from the tip. This indicates that these feathers have grown simultaneously, as is typical of juvenile feathers.
Fig. 40. Turdus merula ad 9 after complete postbr moult, 17 October. A distinct pattern of fault bars is visible on primaries 1 and 2 which is further away from the tip on P 2 than on P 1, indicating that these feathers have grown sequentially. On the other primaries and on the secondaries the pattern of growth bars is faint or rather regular, but slightly displaced against each other.
Fig. 39. Fringilla coelebs ly 9 after partial postjuv moult, 20 September. The distinct fault bar pattern crosses all primaries, secondaries and tertials at similar distances from the tip, indicating that these feathers have grown simultaneously. Fault bars are also present on the juvenile primary coverts, alula feathers 2â&#x20AC;&#x201D;3 and greater covert 1, but not on the postjuvenile greater coverts and alula feather 1.
Fig. 41. Sylvia atricapilla ad 6 after postbr moult, 9 May. This adult shows prominent fault bars on secondaries 2-6 and tertials 7-8 at similar distances from the tip on the right wing only. These feathers have apparently been lost accidentally and re-grown simultaneously. In cases of accidental feather loss, fault bars on the replacement set give no clues to age.
among the feathers of a tract or may be absent on some feathers within a tract. Many birds renew feathers simultaneously during a normal moult (especially rectrices, see section 3.2.3). Feathers may have been lost accidentally, in which case the replacement set has grown simultaneously (Fig. 41). Indistinct irregularities in growth bars may appear by chance at similar distances from the tip. In most individuals, any irregularities in growth bars are confused and one should refrain from constructing ageing arguments from them. Of course, all the feathers of first-year birds which have performed a complete postjuvenile moult show a sequential fault bar pattern.
5.2.2 Differences in extent of moult In many species, the extent of the moults during the first year of life differs from that of the corresponding moults of adults (see chapter 4). For instance, in many species adults perform a complete moult while first-year birds show a partial moult during summer/autumn. In this case, it is sufficient for ageing to recognize whether one or two feather generations are present, without the need to identify the precise feather
generations (e.g. juvenile feathers). In a few species, both first-year and adult birds perform a partial moult, but of consistently different extent thus indicating their age (e.g. Muscicapa striata, see p. 138; Locustella fluviatilis and Acrocephaluspalustris in NE Africa, see section 4.6.2). Differences in the extent of moult between age classes can also be of use when determining the age of birds in active moult, provided that the sequence is known (see sections 3.2 and 4.3).
5.2.3 Differences between postjuvenile and subsequent feather generations In a few species, the feathers which replace the juvenile feathers are conspicuously different from those of subsequent feather generations (e.g. Lanius collurio, see p. 154; Oriolus oriolus, Svensson 1992) and provide a convenient ageing criterion. In Sturnus vuigaris and S. unicolor, the shape and colour of the postjuvenile rectrices, throat and mantle feathers differ on average from those of adults which allows one to age most individuals (Hiraldo & Herrera 1974, Williams 1991, Svensson 1992).
52
Ageing European Passerines
In some species, there are, on average, slight differences between the postjuvenile and subsequent feather generations in the intensity and brightness of colour or gloss and in the width of the light feather fringes (e.g. Eremophila alpestris, Motacilla flava, Luscinia svecica, Phoenicurus phoenicurus, Saxicola rubetra, Sylvia atricapilla, Ficedula parva, Cinclus cinclus, Fringilla montifringilla, Carduelis flammea\ Fig. 42). However, the overlap between first/second-year birds and adults is usually too large to provide reliable ageing criteria for individual birds, Furthermore, in some of these species, the age differences in coloration are confounded by sex differences.
former have been allocated to moult cycle type (3), the latter to moult cycle type (2), (3) and (4), respectively. In the Tables 5â&#x20AC;&#x201D;8, all species of passerines breeding in Europe are listed, except a few breeding in the far east of Europe. For other species, occurring in Europe, the indications on moult in Svensson (1992) and in the Handbooks by Glutz & Bauer (1985, 1988, 1991) and Cramp (1988, 1992, Cramp & Perrins 1993) will allow their allocation to one of the moult cycle types. Each species has been entered in only one of the Tables 5-8, although it may moult according to two moult cycle types. Such cases and other exceptions are indicated in the Tables.
5.3 General ageing criteria in European passerines based on moult
5.3.1 Species with a complete postjuvenile moult in the first summer/autumn: Moult cycle type 1
As shown in the preceding section, ageing on plumage characters relies primarily on the recognition of juvenile feathers and on differences between age classes in the extents of corresponding moults. How long juvenile feathers remain on the bird and how different are the extents of corresponding moults between age classes, depend primarily on the moult cycle (see chapter 4 and Table 3). Therefore, the general plumage ageing criteria are basically similar for birds moulting according to the same moult cycle. In the remainder of this section, we group the European passerines according to their moult cycles and indicate the general ageing criteria they have in common. Being aware of the moult cycle of a species when ageing it has several advantages: (1) it may allow ageing of birds in active moult, something generally neglected in existing ageing guides; (2) it allows a better understanding of unusual or previously unknown moult patterns for the species, and of their implications for ageing; (3) it may allow ageing of species whose ageing criteria have not been studied in detail; (4) it allows easier detection of previously undescribed plumage ageing criteria. However, since in certain species, not all individuals moult according to the-same moult cycle, a knowledge of the possible intraspecific variation in moult cycles, as presented in chapters 3 and 4 and Table 2, is indispensable. For the purpose of ageing, four main types of moult cycles can conveniently be distingushed. They are based on the number and extents of moults up until the last juvenile feather has been replaced: (1) In a few European passerines, all juvenile feathers are replaced in the first summer during a complete postjuvenile moult (section 5-3.1). (2) In many species, part of the juvenile feathers are moulted during the postjuvenile moult in the first summer/autumn and the remainder during the first complete postbreeding moult in the second summer/autumn (section 5.3.2). (3) A number of species present the same moult cycle as in type (2), but with an intervening partial prebreeding moult which may or may not include some of the retained juvenile feathers (section 5.3.3). (4) In some long-distance migrants, only a few or no juvenile feathers are moulted during the postjuvenile moult in the breeding area, the remainder being replaced later during a complete moult in the non-breeding area (section 53.4). There are few birds which do not readily fall within one of these four moult cycle types: those with a seasonally divided moult as well as Carpodacus erythrinus, Emberiza aureola and Phylloscopus trochilus. The
Moult cycle: Members of this moult cycle type (Table 5) replace all the juvenile feathers during the postjuvenile moult in their first summer/autumn. Adults also perform a complete moult at about the same time (Fig. 43). Only Acrocephalus melanopogon and Cisticola juncidis have a partial prebreeding moult which occurs in second-year birds and adults and gives no clue to a bird's age. Ageing before the postjuvenile and postbreeding moults: The juvenile plumages are generally easily recognized by the structure and coloration of the body-feathers. Adults in summer have worn their plumage for almost a year and usually show distinct signs of abrasion and bleaching (Fig. 44-47). Ageing during the postjuvenile and postbreeding moults: If still present, the unmoulted feathers can usually be scored as being juvenile or not by their coloration, structure and wear. The presence of growing remiges is not an ageing criterion. In Panurus biarmicus, the juvenile P 10 (the last primary to be moulted) is considerably longer than the primary coverts, while in adults P 10 only reaches the primary coverts. Ageing after the postjuvenile and postbreeding moults: This is generally not possible on plumage characters, except in Sturnus vulgaris and S. unicolor (see Hiraldo & Herrera 1974, Williams 1991, Svensson 1992). However, some birds exceptionally retain individual juvenile feathers. In most species of this moult cycle type, skull pneumatization is valid until well into the autumn, but not in Alauda arvensis, Lullula arborea and possibly other Alaudidae in which the first fully pneumatized first-year birds appear in September/October (Winkler 1979). In Panurus biarmicus^ skull pneumatization is hardly visible in live birds because of the pigmented skin.
5.3.2 Species with a partialpostjuvenile/Complete postbreeding moult in the breeding area: Moult cycle type 2 Moult cycle: Members of moult cycle type 2 (Table 6) have one complete moult annually just after breeding as adults, while the juveniles perform a partial postjuvenile moult after hatching and before winter or migration (Fig. 48). The only exception is Carpodacus erythrinus which delays the postjuvenile and postbreeding moult until its arrival in the tropics. Extent of moults: In all these species, the postjuvenile moult of bodyfeathers is nearly always complete. On the wing, however, the extent of Fig. 42. 6 Phoenicurusphoenicurus in autumn. The grey, white, black and orange colours on the head and breast are on average more concealed by light fringes in first-year birds (centre and right) than in adults (left). However, only extremes can be aged by the conspicuousness of the coloration. Some adults look like the bird in the centre.
General ageing criteria in European passerines based on moult
summer
autumn/winter
spring/summer
53
autumn/winter
First year oflife
Adults
Fig. 43. Schematic presentarion of the plumage cycle of moult cycle type 1: Species with a complete postjuvenile moult in the first summer/autumn. After the postjuvenile/postbreeding moult, the plumage of both adults and first/second-year birds is composed of one feather generation acquired at about the same time. Only two species perform a partial prebreeding moult (not shown, see Table 5). Key to Fig. 43, 48, 53 and 54: Colours indicate the feather generations acquired by a complete (full arrow) or partial (broken arrow) moult: green = juvenile feathers; red = feathers acquired during the postjuvenile/postbreeding moult in the breeding area; blue = feathers acquired during the prebreeding moult in winter/spring. Dotted areas indicate worn feathers. Table 5. Moult cycle type 1: Species which regularly perform a complete postjuvenile moult in their first summer/autumn. Species in which only some of the individuals perform a complete postjuvenile moult are shown in Table 6 and 7. Chersophilus duponti Melanocorypha calandra Calandrella brachydactyla Calandrella rufescens j Galerida cristata Galerida theklae Lullula arborea Alauda arvensis Eremophila alpestris Cisticola juncidis ' Acrocephalus melanopogon 1
Panurus biarmicus Aegithalos caudatus Sturnus vulgaris Sturnus unicolor Passer domesticus Passer hispaniolensis Passer montanus Petronia petronia Montifringilla nivalis Miliaria calandra
' Some ly perform a partial postjuvenile moult before a complete moult in late autumn (see section 4.4.4). Prebreeding moult occurs in at least some individuals, but its extent is poorly known. ' Prebreeding moult in 2y and ad the postjuvenile moult varies considerably among species, from a few wing-coverts and no greater coverts moulted (e.g. Sitta), through a regular moult of all the greater coverts and usually some tertials as well (Parus major, P. caeruleus, Coccothraustes coccothraustes, Emberiza citrine/la, E. da) to partial, usually eccentric, primary moult (in earlyhatched birds or in Mediterranean populations of some Carduelis species and Loxia curvirostra, see section 4.4). At the extreme, a complete postjuvenile moult may occur (some Loxia curvirostra and
Carduelis Moris]. Within species, the extent of the postjuvenile moult may vary considerably as well. Ageing before the postjuvenile and postbreeding moults: As for members of moult cycle type 1. Ageing during the postjuvenile and postbreeding moults: Birds in active moult of the median coverts, greater coverts and tertials and/or regular, symmetric rectrix moult but without signs of moult of the secondaries and primaries are first-year birds (Fig. 49â&#x20AC;&#x201D;50). Birds with growing primaries and/or secondaries following the basic sequence are generally adults (Fig. 52). However, in some species first-year birds may renew the innermost secondaries (see section 4.3.1) and/or some primaries during the partial postjuvenile moult (Fig. 51; see Table 6 and section 4.4.4). Usually partial primary moult is eccentric, i.e. does not start with P 1 as does the complete moult of the adults, but with one of the central primaries (frequently with P 5-7), but may exceptionally also include the innermost primaries (see section 4.3.3). First-year birds moulting some primaries during the postjuvenile moult typically retain the corresponding primary coverts or replace them irregularly, while adults performing the complete postbreeding moult renew the primary coverts together with the corresponding primaries. Partial primary moult may be observed in more species than shown in Table 6, especially in Mediterranean populations. Thus, when examining actively moulting birds of species which may show partial primary moult as first-year birds, the sequence of primary, secondary and primary covert moult must be observed in detail; skull pneumatization (see appendix)
54
Ageing European Passerines
Fig. 44. Passer domesticus ly at the beginning of the complete postjuv moult, 26 August. Whole wing juv, except P 1-2 and PC 1-2 growing. Juvenile remiges are fresh until renewal at the complete moult. Also on the wing, the colour of the juvenile plumage is different from that of subsequent feather generations.
Fig. 45. Passer domesticus 9 after complete moult, 2 May. Compared with the juvenile wing (see Fig. 44), the wing of adults is differently coloured and worn, especially the tertials, inner greater coverts and outer primaries. and, if still present, retained juvenile body-feathers (which are usually easily identified) are other important ageing criteria. In a few species, some first-year birds (see Table 6) perform a complete postjuvenile moult (following the basic sequence) and the general ageing criteria described for moult cycle type 1 apply. Ageing after the postjuvenile and postbreeding moults: In most species, ageing by plumage characters is based on the recognition of whether one (in adults) or two feather generations (the juvenile and postjuvenile in first/second-year birds) are present (Fig. 48). Thus, one has to decide whether or not there are moult limits between juvenile and postjuvenile feathers. This is possible in most species of this moult cycle type during autumn and winter and in some species with only slight feather wear, up to the time of the complete moult (e.g. Pyrrhula pyrrhula). The few first/second-year birds which have performed a complete postjuvenile moult are inseparable from adults on plumage characters, but may be recognized by skull pneumatization. Moult limits are usually best detected within the greater coverts. Birds with no greater coverts moulted may show moult limits within the median and marginal coverts or colour differences between the renewed median coverts and juvenile greater coverts (e.g. Nucifraga caryocatactes, Jenni 1983). Birds with all the greater coverts moulted must be checked for moult limits within the tertials, rectrices and alula feathers or between the tertials and secondaries as well as between the greater coverts, primary coverts, alula feathers and carpal covert. In
Fig. 46. Sturnus vulgaris ly in juvenile plumage, 8 June. Juvenile wing fresh, uniformly grey, with dull fringes and without gloss.
Fig. 47. Sturnus vulgarised. cT after complete postbr moult, 5 May, Compared with juveniles (see Fig. 46), the wing of adults is worn, glossy and with prominent light fringes.
some species, some individuals show moult limits within the primaries and secondaries and may be determined as first/second-year birds. If valid, skull pneumatization will be the useful criterion for birds in which moult limits are difficult to assess. Although individuals presenting moult limits are generally first/second-year birds, one has to bear in mind that adults of almost every species may, exceptionally, retain individual feathers or interrupt moult before it is completed. In these cases the retained feathers are conspicuously bleached (being at least one year old). The feathers retained are always the last feathers to be moulted during the postbreeding moult, i.e. S 6, P 9, 10 and Al. Some adults at the end of the postbreeding moult may be recognized as such by the sheaths still showing on the last feathers moulted (but beware of partial primary moult of first-year birds). Exceptionally, individual juvenile body-feathers are retained.
53.3 Species with a partial postj uvenilelcomplete postbreeding moult in the breeding area and a partial prebreeding moult in winter I spring: Moult cycle type 3 Moult cycle: Adults following this moult cycle type (Table 7) perform a complete postbreeding moult in the breeding area and a partial
General ageing criteria in European passerines based on moult
Table 6. Moult cycle type 2: Species which perform a partial postjuvenile moult in their first summer/autumn and a complete postbreeding moult as adults. Species in which only some of the individuals do so are shown in Table 7. Ptyonoprogne mpe$tris()
Sitta neumayer6
Bombycilla garrulus* _. . . / 6 Linclus cinclus
Certhia familiaris Certhia hrachydactyla2
Troglodytes troglodytes Prunella modularis Prunella collaris Erithacus rubecula Luscinia luscinia Lusciniamegarhynchos Tarsiger cyanums Phoenicurus ochruros' Phoenicurus phoenicurus Saxicola torquata^ Oenamhe leucura Monticola solitarius6 Turdus torquatus Turdus merulalA Turdus pilaris Turdus philomelos Turdus iliacus Turdus viscivorus Regulus regulus Regulus ignicapillus Parus palustris Parus lugubris Parus montanus Parus cinctus Parus cristatus Parus ater Parus caeruleus1 Parus cyanus 3or Sitta whiteheadi Sitta europaea
Remiz pendulinus2 Garrulus glandarius Perisoreus infaustus Cyanopica cyana}'z Pica pica Nudfraga caryocatactes Pyrrhocorax graculus Pyrrhocorax pyrrhocorax Corvus ^onedula Corvus frugtlegus Corvus corone Corvus corax
Fringilla coelebs Fringilla montifringilla Serinusserinus1'2 Serinus citrinella Carduelis chloris] l23 Carduelis carduelis^2 Carduelis spinus^1 C
*rd?dis â&#x201E;˘â&#x201E;˘ahiâ&#x201E;˘2 Carduelis favirostris Carduelis flammea Carduelis hornemanni Loxia leucoptera^ Loxia curvirostra7 Loxia pytyopsittacus* Carpodacus erythrinus23'10 Pinicola enucleator Pyrrhula pyrrhula Coccothraustes coccothraustes
Emberiza citrinella^ Emberiza cia
1
Postjuvenile moult may include secondaries Postjuvenile moult may include primaries, usually eccentrically 3 Postjuvenile moult may be complete 4 Postjuvenile moult usually in late autumn/winter, extent poorly known 3 Postbreeding moult: some feathers may be retained 6 Some individuals moult some body-feathers, occasionally marginal and median coverts in winter/spring. Thus, there might be a restricted prebreeding moult. Moult pattern highly variable 8 Moult pattern may be as complex as in Loxia curvirostra '} Postbreeding moult regularly overlaps with breeding. Very protracted postjuvenile and postbreeding moult lasts well into winter. 111 No moult before autumn migration in ly and ad. Postjuvenile and postbreeding moult take place in autumn/winter in the tropics. :
prebreeding moult in winter/spring (Fig. 53). Birds in their first year of life have a partial postjuvcnilc moult of variable extent in the breeding area, a partial prebreeding moult in winter/spring and attain the full adult plumage by performing a complete postbreeding moult in their second summer/autumn in the breeding area. This moult cycle type is the most complex one, since part of the juvenile feathers can be replaced during the postjuvenile moult in the first summer/autumn or during the prebreeding moult in the first winter/spring and the remainder during the first postbreeding moult in the second summer/autumn. Due to the many possible combinations of feather generations in both second-year and adult birds (Fig. 53), ageing is difficult in many species. Furthermore, in some species a seasonally divided moult of the remiges occurs. Extent of moults: During the postjuvenile moult, all or most of the body-feathers are generally moulted (except m Anthus campestris). The
55
extent of the postjuvenile moult on the wing varies considerably from none (e.g. many Anthus campestris)^ through all the wing-coverts and often the tertials and rectrices (e.g. Emberiza schoenidus), up to a partial primary moult (e.g. Sylvia melanocephala). In some species, some individuals perform a complete postjuvenile moult (some Mediterranean Sylvia warblers). The postbreeding moult of the adults is usually complete. However, adults may interrupt the moult of the remiges before autumn migration more often than in members of moult cycle type 2 (see section 3.3.3, Table 2 and 7). This occurs regularly in Anthus campestris, A. richardi, Sylvia hortensis, S. nisoria, Lanius nubicus, Emberiza hortulana, E. caesia, less frequently in Ficedula hypoleuca and Sylvia c. communis and only exceptionally in other species. The extent of the prebreeding moult varies from an insignificant spotwise moult of the body or head-feathers, through an extensive renewal of the body-feathers, wing-coverts, tertials and rectrices (e.g. Motacilla flava), up to a partial secondary and/or primary moult (usually eccentric). First-year birds with a postjuvenile moult of limited extent tend to replace more wing-coverts during the prebreeding than during the postjuvenile moult and thus replace all the postjuvenile wing-coverts a second time. There is generally such a large overlap in the extent of the prebreeding moult between adults and first/second-year birds, that differences in extents between the age classes (see section 4.6.1) cannot be used for ageing. Ageing before the postjuvenile and postbreeding moults: As for members of moult cycle type 1. Ageing during the postjuvenile and postbreeding moults: As for members of moult cycle type 2. Species which may perform a partial primary moult or a complete postjuvenile moult (common in Sylvia melanocephala) are listed in Table 7. Ageing after the postjuvenile and postbreeding moults: As for members of moult cycle type 2, but restricted to the time between the completion of the postjuvenile/postbreeding moult and the onset of the prebreeding moult. First/second-year birds which have performed a complete postjuvenile moult are inseparable from adults on plumage characters, but may be recognized by skull pneumatization. Those adults which interrupt their complete postbreeding moult before autumn migration are easily recognized by their very worn and bleached retained remiges (usually secondaries) or alula feathers. The retained secondaries are not always the last to be moulted during a complete moult (see Fig. 11). Ageing after the prebreeding moult: (a) Species with a prebreeding moult restricted to the body-feathers (see Table 7): As in the autumn, the wing of adults still consists of one and that of second-year birds still of two feather generations (juvenile and postjuvenile). Hence, the same ageing criteria as for members of moult cycle type 2 apply, provided that the characters have not faded away due to wear. (b) Species with a prebreeding moult including some wing-coverts: Both adults and second-year birds show a moult limit within the wing-coverts due to the prebreeding moult and, in many cases, it will be difficult or impossible to separate the age classes. The only way is to assign those feathers not moulted during the prebreeding moult (remiges, primary coverts, often outer greater coverts and tertials, occasionally median and marginal coverts) to either the juvenile (thus second-year bird), the postjuvenile or the postbreeding feather generation. Juvenile feathers can often (but not always) be distinguished from the corresponding postbreeding feathers of the adults by their more abraded and bleached appearance. Retained postjuvenile feathers, however, are usually impossible to distinguish from the corresponding postbreeding feathers of the adults. If only prebreeding and postjuvenile feathers are present within a feather tract, without any juvenile feathers, ageing may become very difficult. Within the wing-coverts of some second-year birds (e.g. Motacilla alba), the prebreeding moult is less extensive than the postju-
56
Ageing European Passerines summer
autumn/winter
spring/summer
autumn/winter
First year of life
Adults
Fig. 48, Schematic presentation of the plumage cycle of moult cycle type 2: Species with a partial postjuvenile/complete postbreeding moult in the breeding area (see Fig. 43 for details). First/second-year birds retain part of the juvenile feathers until the first postbreeding moult. After the postjuvenile moult, their plumage is composed of two feather generations, in contrast to the single generation of the adult plumage. The extent of the postjuvenile moult is very variable. In a few species, partial postjuvenile primary moult occurs (second row of ly/2y birds).
Fig. 49. Carduelis cannabina ly 8 in partial postjuv moult, 30 August. MaC postjuv, MeC missing or postjuv. GC 1â&#x20AC;&#x201D;2 juv, rest growing. Rest of wing juv. During summer/autumn, individuals belonging to moult cycle types 2 and 3 with growing greater coverts, but without signs of moult of secondaries and primaries can be determined as first-year birds.
Fig. 50. Parus caeruleus ly in partial postjuv moult, 13 August. MaC postjuv. MeC juv or missing. GC growing, CC postjuv. Al 1 growing. T 8â&#x20AC;&#x201D;9 growing. Rest of wing juv. During summer/autumn, growing greater coverts and tertials, but no growing remiges indicate a first-year bird in species belonging to moult cycle types 2 and 3-
General ageing criteria in European passerines based on moult
Fig. 51. Carduelis chloris ly 6 in partial postjuv moult, 30 August. MaC postjuv. MeC growing. GC 1—9 postjuv, 10 juv. CC postjuv. Al 1—2 shed, 3 juv. T 7+9 juv, 8 growing. P 6 growing, 1—5+7—10 juv. PC and S juv. This bird renews primary 6 eccentrically, but not the corresponding primary covert. This, as well as the facts that primaries 7-9 are not worn and no secondaries are growing, indicates that it is a first-year bird.
venile moult and there are still juvenile coverts present. In these cases, there will be three feather generations among the wing-coverts, e.g. within the greater coverts, from inside to outside, prebreeding, postjuvenile and juvenile coverts. Three feather generations within the coverts is diagnostic of second-year birds. In many species (e.g. some Sylvia warblers) the extent of the prebreeding moult is not well known. Furthermore, the prebreeding moult of some species seems to be subdivided, protracted or to consist of two moults (e.g. Motacillaflava, Sylvia communis, S. cantillans). This may result in the wing-coverts being moulted in an irregular sequence and in a mixture of different degrees of wear spread over the whole feather tract. Such moult patterns are difficult to interpret and no conclusions on age should be drawn. (c) Species with a prebreeding moult including some remiges: Most of these species may interrupt the postbreeding moult before autumn migration and thus show a seasonally divided moult of the remiges. During the winter, adults usually complete the moult of the remiges, but second-year birds may also renew some secondaries or primaries (usually eccentrically). Due to the high variability of these moult cycles (see section 3.3.3 and 4.6.3), it is at present impossible to give any reliable ageing criterion based on the renewal of the remiges. Ageing of some of these birds may be possible by the criteria given above. In the case of partial primary moult, the non-renewal of the corresponding primary coverts usually indicates a second-year bird.
5.3.4 Species with a complete moult in the non-breeding area Moult cycle: All species following this moult cycle type (Fig. 54, Table 8) are long-distance migrants. Most adults and first-year birds perform a partial moult between the end of the breeding season and the onset of autumn migration, and a complete moult in the tropical winter quarters. Within the winter quarters there may be an additional partial moult before or after the complete moult, and the complete moult may be temporarily suspended. Extent of moults: In most species following this moult cycle type, the postjuvenile moult before the autumn migration is of very limited extent (comprising part of the body-feathers and occasionally some wing-coverts) or completely absent (see section 4.4.2). The same holds for the postbreeding moult of adults, but some may include some tertials and rectrices, occasionally some secondaries (e.g. Muscicapa striata, Oriolus oriolus, Phylloscopus bonellt) or the innermost primaries (e.g. hirundines, Acrocephalus arundinaceus, Lanius senator). Among
57
Fig. 52. Sylvia atricapilla ad 9 in complete postbr moult, 1 September. Whilst renewing greater coverts and tertials, adults belonging to moult cycle type 2 and 3 also moult their primaries, following the basic descendant sequence.
first-year birds, only the hirundines may rarely renew some primaries before the autumn migration. Adult Phylloscopus trochilus regularly perform a complete postbreeding moult (sometimes retaining some secondaries) and the same has been observed in a very small percentage of adult Sylvia borin. In the tropics, the adults only of some species show a partial moult in autumn/early winter (e.g. Locustella fluviatilis, Acrocephalus palustris, not shown in Fig. 54). The complete moult may be suspended within the winter quarters, but it is not yet clear whether this occurs in both first/second-year birds and adults. In some species, both age classes may occasionally retain some secondaries (e.g. Muscicapa striata, Oriolus oriolus). Second-year Lanius senator regularly retain the innermost primaries and some secondaries. The occurrence and extent of an additional partial prebreeding moult (e.g. in many Acrocephalus warblers) is poorly known (not shown in Fig. 54). Ageing before the postjuvenile and postbreeding moults: In many species, the juvenile plumage is not easily recognizable by its colour or structure. However, juveniles have a fresh plumage while that of the adults is usually worn (see below). Ageing during the postjuvenile and postbreeding moults in the breeding area: Since the postjuvenile and the postbreeding moults are usually of limited extent, the same ageing criteria as before or after the postjuvenile/postbreeding moult apply (exceptions are Phylloscopus trochilus and some Sylvia borin). Ageing after the postjuvenile and postbreeding moults and before the complete moult in the winter quarters: In most species, ageing relies on the difference in wear between first-year birds and adults. First-year birds have worn their juvenile and postjuvenile feathers for only several weeks or a few months and have a fresher plumage than adults who have worn those feathers not moulted during the postbreeding moult for half a year or more, including the breeding season, and generally show quite abraded and bleached feathers. Abrasion is especially strong in species living in dense vegetation and most evident on the tertials, tips of the outer primaries and wing-coverts. Since both adults and first-year birds may perform a partial moult before the autumn migration, both age classes may show moult limits. Due to the greater difference in age between the two feather generations, however, any moult limits are more prominent in adults than in first-year birds. Furthermore, birds which have moulted some remiges are adults (except in hirundines). In many species, juvenile bodyfeathers are still present and may be easily recognized (e.g. hirundines, Muscicapa striata, Lanius spp.).
58
Ageing European Passerines
A summer
autumn/winter
spring/summer
autumn/winter
First year of life
Adults
B summer First year of life
Adults
autumn
winter
spring/summer
autumn
General ageing criteria in European passerines based on moult
59
Fig. 53. (Opposite) (A) Schematic presentation of the plumage cycle of moult cycle type 3: Species with a partial postjuvenile/complete postbreeding moult in the breeding area and a partial prebreeding moult in winter/spring (see Fig. 43 for details). After the postjuvenile/postbreeding moult, the plumage of first-year birds is composed of two feather generations, while that of the adults generally of only one, as in members of moult cycle type 2. The extent of the postjuvenile moult is very variable, ranging from only a few body-feathers up to a partial postjuvenile primary moult (not shown, see Fig. 48). After the prebreeding moult, the composition of the plumage depends on the extent of the prebreeding and postjuvenile moult. Hence, many combinations of feather generations in both second-year and adult birds are possible, of which only the most typical ones are shown. Adults may show one (upper bird) or two (lower bird) feather generations within the feathers of the body and one (not shown) or two feather generations in the wing. Second-year birds show one or two feather generations within the bodyfeathers, i.e. prebreeding (upper bird) or prebreeding and postjuvenile bodyfeathers (lower bird); two or three feather generations within the wing-coverts, i.e. juvenile and postjuvenile (not shown) or juvenile and prebreeding (upper bird) or postjuvenile and prebreeding (not shown) or juvenile, postjuvenile and prebreeding wing-coverts (lower bird); one or rarely two feather generations within the remiges, i.e. juvenile (upper and lower bird) or juvenile and postjuvenile or juvenile and prebreeding remiges (not shown). (B) An example of a bird showing a seasonally divided moult of remiges, as it occurs in some Sylvia warblers (for other types of seasonally divided moult of remiges see text, Table 2 and 7).
These general rules do not apply to Phylloscopus trochilus in which both adults and first-year birds have fresh plumages (see p. 136) and to the very few Sylvia borin which have performed a complete postbreeding moult (see p. 127). In Locustella fluviatilis and Acrocephalus palustris, adults perform a partial moult in autumn/early winter in NE Africa which includes the outer primaries, part or all of the wing-coverts and the tertials (in L. fluviatilis) and the body-feathers (in A. palustris and L fluviatilis). Firstyear birds do not show this moult, so it represents an ageing criterion after this partial moult and before the complete moult further south (Pearson 1989). Ageing after the complete moult in the winter quarters: Adults and second-year birds are usually inseparable on plumage characters at this time. Both age classes may retain some secondaries (e.g. Oriolus oriolus). Only in Lanius senator and possibly some L. minor, are second-year birds distinguished from adults by the retained innermost primaries, or at least some primary coverts (see Fig. 36 and 37).
Table 7. Moult cycle type 3: Species which perform a partial postjuvenile moult in their first summer/autumn or a complete postbreeding moult as adults in the breeding area and a partial prebreeding moult in winter/spring. In some species, seasonally divided moult of remiges occurs.
Table 8. Moult cycle type 4: Species in which both age classes perform a complete moult in the non-breeding area. In some species, the prebreeding moult may be incomplete.
A nthus campestris' " 5 "'' Anthus trivialis*3'" Anthus pratensis Anthus cervinus Anthus spinoletta'' Motacilla flava'' Motacilla citreola Motacilla cinerea Motacilla alba2'* Luscinia svecica* Saxicola rubetra Oenanthe isabellina** Oenanthe oenantke9 Oenanthe pleschanka* Oenanthe hispanica* Monticola saxatilis9'12 Cettiacetti™ Sylvia sarda™'{2 Sylvia undata23^2 Sylvia conspicillata2™ Sylvia cantillans**7" Sylvia melanocephala2'-* Sylvia melanothorax2'*A Sylvia rueppelli2'* 1
Sylvia honensis6 !' Sylvia nisoria6'" Sylvia curruca^1 Sylvia c. communis67'" Sylvia atricapilla™M Phylloscopus collybita2'*' Ficedula parva Ficedula semitorquata'' Ficedula albicollis'' Ficedula hypoleucab~u Tichodroma muraria^ Lanius excubitor3'™'12 Lanius nubicus6"11 Calcarius lapponicus^ Plectrophenax nivalis* Emberiza cirlus*'& Emberiza hortulana^^ Emberiza caesia*3 Emberiza rustica}1 Emberiza pusillal2 Emberiza aureola**'1* Emberiza schoeniclus2'^
Postjuvenile moult restricted to part of the body-feathers or absent Postjuvenile moult may include secondaries •' Postjuvenile moult may include primaries, usually eccentrically 4 Postjuvenile moult may be complete * Postbreeding moult often suspended within primaries, completion in tropics. A few individuals postpone all primary moult until arrival in the tropics. 6 Postbreeding moult may be incomplete (usually some or all secondaries retained) 7 Postbreeding moult: some primaries may be retained " Prebreeding moult restricted to part of the body-feathers or completely absent " Prebreeding moult includes body-feathers, but only rarely wing-coverts and tertials 10 Prebreeding moult occurs only in some individuals 1 ' Prebreeding moult may include secondaries (in some species primaries) in 2y and ad (in Emberiza hortulana possibly only in ad) '" Prebreeding moult poorly known 13 No moult before autumn migration in ad and ly. Postjuvenile and postbreeding moult takes place in autumn at staging site. :
Riparia riparia1'2 Hirundo rustica12 Hirundo daurica2 Delichon urbica1'2 Cercotrichas galactotes'' Locustella naevia2'* Locustella fluviatilis** Locustella luscinioides" Acrocephalus paludicola Acrocephalus schoenobaenus Acrocephalus agricola Acrocephalus dumetorum* Acrocephalus palustris ^ Acrocephalus scirpaceus Acrocephalus arundinaceus2 Hippolais pallida Hippolais caligata
Hippolais olivetorum Hippolais icterina Hippolais polyglotta Sylvia communis icterops2 Sylvia borin2'17 Phylloscopus trochiloides Phylloscopus borealis Phylloscopus bonelli2^7 Phylloscopus sibilatrix2'1 Phylloscopus trochilus™ Muscicapa striata2'*'7 Oriolus oriolus2 )7 Lanius collurio2^ Lanius minor Lanius senator2* Emberiza melanocephala
1
Postjuvenile moult before autumn migration may rarely include innermost primaries. Postbreeding moult before autumn migration may include innermost primaries (very rarely eccentric primary moult). 3 Postbreeding moult before autumn migration may include secondaries. * Postbreeding moult before autumn migration may be complete. f Partial moult of body-feathers in NE Africa before complete moult further south in ad, 2
6 7
but not in ly.
Partial primary moult in NE Africa before complete moult further south in ad, but not in ly.
Prebreeding moult may be incomplete in 2y and ad: some secondaries retained. Prebreeding moult may be incomplete (probably in 2y): innermost primaries retained. ' Prebreeding moult usually incomplete in 2y, but not in ad: secondaries, primary coverts and innermost primaries retained. !0 Ad have a biannual complete moult (some secondaries may be retained during the post-breeding moult), ly/2y a partial postjuvenile moult and a complete prebreeding moult 1 ' Moult strategy variable and not fully understood. Ageing difficult. 8 J
60
Ageing European Passerines
summer
autumn
winter
spring/summer
autumn
First year of life
Adults
Fig. 54. Schematic presentation of the plumage cycle of moult cycle type 4: Species with a complete moult in the non-breeding area (see Fig. 43 for details). First-year birds retain large parts, occasionally all, of the juvenile plumage until the first complete moult in the winter quarters. After the postjuvenile moult, their plumage is composed of one or two feather generations, i.e. juvenile (upper bird) or juvenile and postjuvenile feathers (lower bird), which differ in age by several weeks only. After the postbreeding moult in the breeding area, the plumage of the adults is usually also composed of two feather generations, i.e. postbreeding and prebreeding feathers (lower bird), which differ in age by about six to nine months (Phylloscopus trochilus see text). Some adults do not moult before autumn migration and thus show a completely old plumage (upper bird). After the moults in the winter quarters, second-year birds and adults usually have the same plumage, i.e. composed of one feather generation, occasionally of two when having performed an additional partial prebreeding moult.' The complex moults of some species in the winter quarters are not shown (see text and Table 8).
CHAPTER 6
Species Accounts Presentation of the data and directions for use The species accounts present quantitative data on the extent of moult in 58 species from our own observations, as well as summarizing data from the literature. Ageing criteria based on moult are thus derived and supplemented with notes on other important ageing criteria. Colour photographs of extended wings illustrate the range of completed moult patterns and the corresponding plumage criteria which indicate a bird's age. Except for moults in tropical winter quarters, which may occur during early or late winter, we have not given data on the timing of moult. First, in most species the timing of the postbreeding/postjuvenile moult is broadly set by the timing of the breeding season and subsequent autumn migration (for more detailed information see Ginn & Melville 1983 as well as Glutz & Bauer 1985, 1988, 1991 and Cramp 1988, 1992, Cramp & Perrins 1993). Second, the timing of moult often varies considerably between individuals in a population and between populations. Consequently, general remarks on the timing of moult are of little help when ageing individual birds, since the state of the plumage must be determined by inspection for each individual (e.g. whether it has not yet moulted, is moulting or has completed moult).
Material Each species account presents a quantitative description of the extent of the postjuvenile, postbreeding and, if present, of the prebreeding moult. Only birds which had completed moult were included. Data were collected in summer/autumn (usually late July until the end of October) from live birds caught at several bird ringing stations in Switzerland: on the Alpine pass of Col de Bretolet (46°09'N/6°47'E) in 1980-1982 and 1988-1991 (and for a few species from additional years also); near Portalban (46°55'N/6°56'E) in 1987-1989; and near Grone (46°15'N/7°26'E) in 1984-1985. Some additional data were collected from other places in Switzerland and from Swiss birds in the collection of the Natural History Museum, Basel. Data from winter are mainly from the collection of the Natural History Museum, Basel. Spring data were collected at bird ringing stations near Iragna, Switzerland, (46°20'N/8°58'E) in 1990 and on Ventotene Island, Italy (40°48'N/13°25'E) in 1989 and 1991, as well as from the collection of the Natural History Museum, Basel. For a few species, skins from Europe in the British Museum (Natural History) were inspected (Anthus campestris, A. pratensis spring, M. cinerea spring, Luscinia s. $ve~ cica, Turdus t. torquatus, T. iliacus, Sylvia curruca spring, Musdcapa striata spring and adult autumn).
Relevance of the data As shown for many species (see section 4.4.3), the extent of a partial moult may vary according to a bird's geographical origin. In the case of predominantly sedentary species, the average extent of moult may be larger or smaller in areas other than in Switzerland. For migratory species with large sample sizes, our data probably describe the whole range of moult extent shown by birds from N Europe to south-central
Europe, since we mainly examined birds on migration. For migrants with small sample sizes, moult patterns which rarely occur in Switzerland may be missing. Since one might expect that most autumn migrants examined by us originate from central Europe, the quantitative data on moult extent are probably biased towards the average for that part of Europe. Generally, birds from N Europe can be expected to show a more limited average extent of moult than that found in our Swiss material, while birds in S Europe may show a more extensive moult and perhaps also as yet undocumented moult patterns. Data from the literature which give clues to any geographical variation are presented. However, since hatching date seems to be the predominant factor determining the extent of postjuvenile moult (see section 4 A3) considerable variation would be expected in all areas.
Presentation and analysis of the data For each species treated, the extent of moult is described by a series of summary statistics and, usually, a schematic wing diagram. For the analysis of the variation in moult extent, we took into account especially those factors which may be of interest to ringers. If sample sizes were large enough, the data have usually been analysed for differences between sites and the sexes and for seasonal trends. Differences between years could only be analysed with large data sets since there was usually an effect of season as well. However, differences between years were not usually detected; exceptions are given in the species texts. Summary statistics on the extent of moult: Generally, the proportion of birds which have moulted a given number of feathers of a tract after completion of moult is presented. If there is no mention of the bodyfeathers, they are usually all moulted. Within the wing and tail, only the feathers renewed are listed, those not mentioned have not apparently been replaced. For the number of greater coverts moulted, the range, arithmetic mean and mode (most frequent value) are given. Furthermore, the proportion of birds which have moulted none or all greater coverts is indicated, since this is of particular interest for ageing. The sample sizes are usually larger for greater coverts than for the other feather tracts, since we started our study on the moult of the greater coverts first and only included the other feather tracts of the wing in later years. However, data from any one feather tract was always collected over the entire migratory season, so avoiding any bias due to seasonal trends. Schematic wing diagrams: Hatchings indicate the proportion of individuals which have moulted a given feather or feather tract after completion of moult (for sample sizes see the summary statistics). This allows recognition of the variation in moult extent and the places where moult limits are to be expected. In the case of the marginal and median coverts, the entire feather tract is considered and the percentage given is reached by summing the percentage of birds which have moulted all the feathers of the tract plus half the percentage which have moulted part of the tract. The schematic wing diagrams refer to birds caught in Switzerland, thus exclude particular moult patterns occurring only in S Europe which are mentioned in the text.
62
Species Accounts
Graphs of the relationship between the extent of moult in different feather tracts: For those species with samples of sufficient size, the patterns of moult and their variability are shown by graphs showing the relationships between the moult extent of the various feather tracts of the wing. The number of greater coverts moulted is taken as a reference (x-axis) against which the percentage of individuals which have moulted one or more feathers of other tracts are shown. Only birds whose moult is completed and for which all feather tracts have been inspected are included. Graphs showing the seasonal variation of moult extent: In most species, there is a decrease in the extent of moult during autumn migration (see section 4.4.3). To save space, this trend is usually only shown for the extent of greater covert moult, although in many species it is also observed in other feather tracts. The data are usually grouped into fiveday periods (Table 9) or, in the case of small sample sizes, into ten-day periods or by month. Depending on the number of greater coverts moulted, the percentage of individuals which have moulted a given number of greater coverts or the mean number of greater coverts moulted after completion of moult is indicated. In the latter case, lines indicate the 10â&#x20AC;&#x201D;90th percentiles and thus indicate 80% of the birds. If significant differences in moult extent between sexes have been observed, data are given for both sexes separately. Statistical tests: For all species with sufficient data, differences in the extent of moult between sites and changes with season have been tested for independence by chi-square tests. Usually, there was no site effect. In species whose sex can be determined, the extent of moult was analysed for the effects of sex and season by fitting a log-linear model to the three-way contingency table (sex, season, number of greater coverts moulted) to test the interactions for significance. An analogous procedure was used when testing for effects of site and season and when testing large data sets for differences between years, seasons and sex. Differences significant at the P = 0.05 level (two-tailed) have been called significant in the text.
Third, for birds before or during the postjuvenile/postbreeding moult the general criteria given in sections 5-3.1-5.3.4 can be used. For birds after the postjuvenile/postbreeding moult and after the prebreeding moult, those given in the species accounts apply. The sections 'Comments on ageing' give ageing criteria relative to moults, not seasons, since plumage criteria are dependent on moult and since the timing of moult is often variable. Use as many criteria as possible (for skull pneumatization see the appendix). The ageing criteria given apply in the first place to central European populations. According to the indications given on geographical variation in moult extent, the plumage criteria may be weighted and adapted to the birds to be examined. Care has been taken to explain the plumage ageing criteria for the whole range of moult extent, not just the most typical ones. However, be aware of the possibility that the extent of moult may be more or less than given in the species accounts, especially when working in Mediterranean or northern areas. Also be aware that due to early hatching dates, first-year birds may complete skull pneumatization in S Europe earlier than indicated by our Swiss material. Additional information may be obtained from part I of this book via the species index, which may be especially useful when examining a bird showing an unusual moult pattern. In this case, it may be useful to take a series of photographs, i.e. of the whole bird in the hand, of both entire wings and, if indicated, of parts of the wing (when spreading out the wing, place your fingers on the basal parts of the outer primaries, but not on the primary coverts; place all the feathers in their correct position; take the pictures against a background of medium shade, e.g. green vegetation). Table 9. Five-day periods according to Berthold (1973), grouped by decades (ten-day periods). Jan 1-5 Jan 6-10
May 1-5 May 6-10
Aug 29-Sep 2 Sep 3-7
Jan 11-1 5 Jan 16-20
May 11-1 5 May 16-20
Sep8-12 Sep 13-1 7
Jan 2 1-25 /an 26-30
May 21-25 May 26-30
Sep 18-22 Sep 23-27
Procedure of ageing
Jan31-Feb4 Feb 5-9
May 31-Jun4 Jun 5-9
Sep 28-Oct 2 Oct 3-7
This book is intended for users with a certain basic knowledge and as a complement to other ageing guides. For instance, the determination of the species is taken for granted. Ageing criteria other than plumage characters are not illustrated and the user is referred to other ageing guides, notably that by Svensson (1992). When ageing an individual of a given species, the following points should be borne in mind. First, when ageing on plumage characters, begin by understanding the moult cycle of the species concerned, which can be looked up in section 5.3. This provides the general plumage ageing criteria. We are convinced that it is vital to understand the moult cycle of a species when ageing on plumage characters and that the mere application of a set of rules may be misleading. Second, determine the state of the plumage of the bird, i.e. whether it is before, during or after the postjuvenile/postbreeding or the prebreeding moult. This may appear trivial in most cases, but is an important step which, in our experience of instructing ringers, may prevent some serious mistakes.
Feb 10-14 Feb 15-19
Jun 10-14 Jun 15-19
Oci 8-12 Oct 13-17
Feb 20-24 Feb25-Marl
Jun 20-24 Jun 25-29
Oct 18-22 Oct 23-27
Mar 2-6 Mar 7- 11
Jun 30-Jul 4 Jul 5-9
Oct 28-Nov 1 Nov 2-6
Mar 12-16 Mar 17-21
Jul 10-14 Jul 15-19
Nov 7-1 1 Nov 12-16
Mar 22-26 Mar 27-31
Jul 20-24 Jul 25-29
Nov 17-21 Nov 22-26
Apr 1-5 Apr 6-10
Jul30-Aug3 Aug4-8
Nov 27-Dec 1 Dec 2-6
Apr 11-1 5 Apr 16-20
Aug9-13 Aug 14-18
Dec 7- 11 Dec 12-1 6
Apr 21-25 Apr 26-30
Aug 19-23 Aug 24-28
Dec 17-21 Dec 22-26 Dec 27-31
Riparia
riparia
63
Riparia riparia Sand Martin Extent of postjuvenile moult The complete postjuv moult usually begins after arrival in the wintering area, but moult of body-feathers can start while still in Europe (Bub & Herroelen 1981, own obs.) and may continue during the first part of migration (own obs. on Col de Bretolet). Exceptionally, it includes some MaC, MeC and the innermost one or two GC. The only indications of ly starting primary moult in Europe are provided by Belman (in Mead 1980) from Spain and Greece. Moreover, four ly caught at a roost in N Italy during August/September showed renewed or growing P 1, P 1-2 or P 1-3 (F. Spina in lift.). Thus, central European ly generally migrate to Africa in complete or nearly complete juvenile plumage and the complete moult is interpreted as a complete postjuv moult in the winter quarters. Estimates of moult duration of ad and ly in Africa vary between 141 days in Ghana, 121 days in Uganda and Zambia (Mead 1980) and 135 days in Zambia (D.M. Francis in Ginn & Melville 1983). In Kenya and Uganda, moult lasts from about late October/November to mid March/mid April (Ginn & Melville 1983). At the end of February, Zambian birds had renewed 75% of the P, half of the S and 30% of the R. Only one bird out of 43 had already finished its flight feather moult (Loske&Ledererl988).
Fig. 55. ly in juv plumage, 19 September. Whole wing juv. T broadly fringed whitish. Smaller light fringes are present on GC, MeC and MaC.
Extent of postbreeding moult The complete postbr moult usually begins after arrival in the wintering area, but moult of body-feathers, wing-coverts, T, P, perhaps R and exceptionally S can start while still in Europe. In contrast to ly, a very small percentage of ad regularly starts P-moult in Europe. Such records are reported from NW Germany (two out of 450; Bub & Herreolen 1981), Britain (1.9%, N=3465, Mead 1980), Belgium (two records in Bub & Herroelen 1981), Sweden (one out often, Persson 1979), N Italy (14 ad and four unaged birds, F. Spina in lift,), Rumania (three out of 18, Csorgo 1992) and Switzerland (one record from Col de Bretolet). Those beginning P-moult in Britain (Mead 1980, N=79) usually had renewed P 1 or P 1—2 (85%), and the four most advanced birds P 1—4 and 1—5. These four birds and an ad with two renewed P had also started to replace S. About half of the birds with new P had also renewed some T, and one bird some R. The birds from Italy had mostly P 1—2, or at most P 1—3 growing or renewed. The high percentage (10%) of birds with new R in July in Bub & Herroelen (1981) probably includes accidental replacement and not regular moult. One bird from Col de Bretolet with renewed P 1—2 also had growing CC and A l l .
Fig. 56. Ad before postbr moult, 5 September. Innermost MaC and MeC, as well as GC 8 recently renewed. Rest of wing acquired during the last postbr moult in winter. T and all wing-coverts without light fringes.
Extent of prebreeding moult Whether the renewal of body-feathers starting in March described by Pearson (1971) indicates an inconspicuous prebr moult is still uncertain. Comments on ageing in summer and autumn ly: T, GC, MeC and MaC broadly fringed light rufous or whitish. Whole plumage fresh. Ad: GC, MeC, MaC and T without or with only very narrow light fringes. Plumage generally worn. After the complete moult in the winter quarters, 2y and ad are indistinguishable on plumage characters.
Fig. 57. 2y/ad after complete postjuv/postbr moult in winter, 25 April. Whole wing postjuv/postbr. After the complete moult in the winter quarters, ageing by plumage is no longer possible.
64
Hirundo rustica
Hirundo rustica Swallow Extent of postjuvenile moult ly and ad usually perform a complete moult in the winter quarters. Whether some of the body-feathers are renewed twice, as in Delichon urbica^ is not known. This complete moult in the winter quarters is interpreted as a complete postjuv moult in ly and a complete postbr moult in ad. Some ly start renewing body-feathers in Europe and, according to our observations on Col de Bretolet, continue doing so during the first part of migration. Rarely, some innermost MaC and MeC are also moulted. The only examples of ly starting P-moult north of the Mediterranean are two birds with growing or new P 1 from England (Mead 1975) and one bird with growing P 1 from Scotland (Cameron & Lynch 1983). Furthermore, at a roost in N Italy, four ly out of 6187 birds (ly and ad) were found with renewed or growing P 1 or P 1—2 in August/September (F. Spina in lift.). Compared with other small passerines, moult duration of ly and ad is very long, estimations varying between 4.5—5 (Broekhuysen & Brown 1963, Stresemann & Stresemann 1968c) and 6-6.5 (de Bont 1962, Kasparek 1976, Francis 1980) months. In Zambia (Francis 1980) and Zaire (Herroelen 1960, de Bont 1962) ly started moulting four to six weeks later than ad, whereas in South Africa there was no significant difference (Broekhuysen & Brown 1963). In all trans-saharan areas studied, many Swallows, presumably mostly 2y, were still moulting in April when northward migration had already started (summarized in Glutz & Bauer 1985). Hence, it is not surprising that some spring birds in Europe have been found with still growing outer P and/or R (von VietinghofT-Riesch 1955> Verheyen in Herroelen 1960, Loske 1984). One bird from Switzerland even interrupted wing-moult at P 8, retaining P 9 on 18 June (skin in Natural Hist. Museum, Basel). Two migrants from Ventotene, Italy from early May showed still growing (score 4) P 9, S 6 and R 6 (F. Spina in litt.).
score 6, some score 4 and 5); ly in early October usually show scores 1-4, some 5-7 (Winkler 1979). Thus scores 1-3 can safely be attributed to ly, scores 4—7 could be either ly or ad. After the complete moult in winter, 2y and ad are indistinguishable on plumage characters.
Fig. 58. ly in juvenile plumage, 19 September. Whole wing juv. Only MaC with some blue gloss. Rest of wing dark brown.
Extent of postbreeding moult Usually a complete moult in the winter quarters (see above). Moult of body-feathers can start in Europe and continue during the first part of migration; it may also include some MaC and MeC and, mainly in birds with P-moult, T 8. In contrast to ly, a small number of ad regularly begin P-moult in Europe. The percentages reported are 2.8% for Switzerland (Winkler 1975), 2.6% for Belgium (M. de Haen & P. Herroelen in Glutz & Bauer 1985), around 10% for S Germany (estimate, Kasparek 1976) and 19% for Spain (Pimm 1970) as well as 56 ad and two unaged birds out of 6187 (1 y and ad) caught in August/September at a roost in N Italy (F. Spina in lift.). Most of the birds examined had only P 1 or P 1-2 growing or new, the most advanced, in Spain, showed renewed P 1-4. One bird from Switzerland with renewed P 1 —2 had also moulted S 1 on one wing.
Fig. 59. Ad 9 before postbr moult, 2 October. GC 5 recently replaced. Rest of wing acquired during the last postbr moult in winter. Although bearing about half a year's wear, the wing is distinctly more glossy than in ly. GC 8—10 seem to be newer than 1—4 and 6—7, but show the same degree of abrasion as the adjacent 6-7.
Comments on ageing in summer and autumn ly: Upperparts and wing-coverts dark brownish-blue, only faintly glossy. Forehead and throat orange. Length of outermost tail-feather 60-75 mm, no overlap with ad 9 . Ad: Upperparts and wing-coverts glossy metallic-blue with a violet tinge. Forehead and throat mahogany. Length of outermost tailfeather over 75 mm. Skull pneumatization is of limited value as an ageing criterion in autumn. Many ad (29%) do not complete skull pneumatization (mainly
Fig. 60. 2y/ad 9 after complete postjuv/postbr moult in winter, 16 April. Whole wing postjuv/postbr. After the complete moult in the winter quarters, ageing by plumage is no longer possible. Fresh wing-coverts with prominent metallic gloss.
Delichon urbica
Delichon urbica House Martin Extent of postjuvenile moult The complete moult usually starts in Europe with the replacement of body-feathers, and exceptionally P. Generally remiges are only renewed after arrival in the winter quarters. In Europe, moult of body-feathers is frequent and, according to our observations on Col de Bretolet, can continue during at least the first part of autumn migration. It does not apparently include wing-coverts and is best observed on the rump, where the white feathers of the juv plumage are replaced by light brown ones. Of 75 birds caught around mid September on Col de Bretolet, 12% had changed at least two thirds or all rump feathers, 53% showed some new rump feathers, 29% had moulted some feathers of other body tracts and 5% had not yet started postjuv moult. The only indications of ly starting P-moult in Europe come from Switzerland (five out of 3705 with new P 1, Winkler 1975), Portugal (two out of seven with growing P 1-2, Mead 1975) and S Spain (Hill 1992). The few moult data from Africa indicate a flight feather moult lasting from November to April (South Africa). In November about 60% (N=107, mostly ly) had started P-moult in Transvaal, the most advanced birds showing growing P 5â&#x20AC;&#x201D;6 (Skead & Skead 1970). By mid April near Cape Town, 21 out of 52 birds (not aged) were in the last stages of P-moult, and 41 had still growing outer tail-feathers (Broekhuysenl953).
65
Comments on ageing in summer and autumn ly: T broadly tipped white. Crown without metallic gloss. Ad: T without or with only very faint white tips. Crown with metallic gloss. Skull pneumatization is of limited value as an ageing criterion in autumn. Many ad (43%) do not complete skull pneumatization (mainly score 6, some score 4 and 5); ly in early October usually show scores 1-3, some 4-7 (Winkler 1979). Thus scores 1-3 can safely be attributed to ly, scores 4â&#x20AC;&#x201D;7 could be either ly or ad. After the complete moult, 2y and ad birds are indistinguishable on plumage characters.
Fig. 61. ly in juv plumage, 10 September. Whole wing juv. T with distinct white tips.
Extent of postbreeding moult Similar to ly, the complete moult usually starts in Europe with the replacement of body-feathers, rarely P and T and, exceptionally, S and GC. Remiges are generally only renewed after arrival in the winter quarters. The beginning of P and T-moult was recorded in 45 (5%) of 948 ad in Switzerland. Ten of these birds had only replaced T 8, the others had renewed or growing P 1 or P 1-2, occasionally together with T 8, and the most advanced bird had moulted P l^i, S 1 and all T (Winkler 1975). In Portugal three out of five ad House Martins were found with renewed P 1 or 1-2 (Mead 1975, Mead & Watmough 1976). From S Spain, Hill (1992) reported that probably all ad renewed P partly, rarely all (usually three to six, range one to nine), many the T and some S; usually only one P was growing at the time, rarely two. The majority was still in active moult of remiges when departing. A migrant from 16 September on Col de Bretolet with a new P 1, growing P 2, new T 8 and GC 7 and some growing body-feathers also demonstrates that moult can continue at least into the first part of autumn migration.
Fig. 62. Ad before postbr moult, 18 September. Whole wing acquired during the last postbr moult in winter. T without white tips.
Extent of prebreeding moult: 2y and ad The prebr moult seems to coincide with the last stages of the postbr/postjuv flight feather moult. This is suggested by the observations of Broekhuysen (1953) near Cape Town who found moult of body-feathers in 94% of 52 birds having finished or nearly finished their flight feather moult. In comparison, only 8.6% of the Swallows examined at the same time showed moult of body-feathers. In 43 of the 49 House Martins with growing body-feathers, moult extended over the whole body, indicating that the prebr moult may comprise all body-feathers. Whether it also includes other feather tracts is not known. The prebr moult results in a change of the rump colour from light brown to white.
Fig. 63. 2y/ad after complete postjuv/postbr moult, 22 April. Whole wing postjuv/postbr. After the complete moult m the winter quarters, ageing is no longer possible. Both age groups may show faint white tips on T. In this bird, P 1-2 and PC 1-2 are more bleached than the rest of the wing. These feathers have most probably been already renewed in Europe, before autumn migration.
66
Anthus campestris
Anthus campestris Tawny Pipit Extent of postjuvenile moult Body-feathers: only partially moulted (cf. Natorp 1925). Some ly migrate in almost complete juv plumage, others moult up to three quarters of the body-feathers. MaC: about half of the ly moult some, the rest moult none. MeC: about one third of the ly moult part, the others moult none, GC: usually not moulted. Only one out of 18 ly had GC 9 renewed. Extent of postbreeding moult The postbr moult was studied by Stresemann & Stresemann (1968a) and Kriiger (1989). Presumably, most northern and central European ad suspend moult of the remiges before autumn migration (Natorp 1925, Kriiger 1989) and resume it in the wintering area, sometimes as early as October/November (Stresemann & Stresemann 1968a). Other birds, however, complete the postbr moult in the breeding area (Stresemann & Stresemann 1968a). These are probably birds from more southern populations (Roselaar in Cramp 1988). There are also indications that some birds may moult all remiges in the wintering area (Kriiger 1989, Svensson 1992). All eight migrants studied in Switzerland showed suspended moult. The bird with the least extensive moult only renewed P 1, T 8 and R 1, the bird in the most advanced stage P 1â&#x20AC;&#x201D;5, T 7â&#x20AC;&#x201D;9 and R 1+6. One bird with four P and all T moulted had also renewed S 6. Otherwise, no S were moulted. All birds renewed the body-feathers completely, or almost so, and most of the MaC. Only one bird renewed all MeC, the others only a few. One bird renewed nine, another seven, the others only a few inner GC.
moult. Moult limits in spring birds (Fig. 71) show that MaC, MeC and GC are moulted at least partially during the prebr moult (N=4). In 2y, as in ad, it is often impossible to judge in spring whether feathers have been renewed during a possible resumption of the postjuv moult in the winter quarters or during the prebr moult. If all feathers moulted in the wintering area are taken together, a very extensive partial 'winter' moult results comprising all MaC, MeC and GC (only one 2y had retained juv GC 1, Fig. 66), sometimes CC and Al, always all T and R, mostly S 6 (one 2y S 1-2+5-6, Fig. 67) and in two birds eccentrically one or two P (one bird P 7, one P 5+7, Fig. 68 and 69) (N=6). Comments on ageing after prebreeding moult In spring, ageing is difficult and not always possible. Moult limits due to the prebr moult occur in 2y and ad. Often, 2y can be distinguished from ad by having more bleached remiges and by the shape and coloration of the PC. The inner PC of 2y typically are more bleached and pointed and have a distinct white terminal fringe (Fig. 66). Those of ad are darker, more rounded and have ill-defined brownish or buffish fringes (Fig. 70 and 71).
Comments on ageing after postjuvenile and postbreeding moult in the breeding area Best criteria: In late summer and autumn, ageing in the breeding area is easy, since ly always show many juv body-feathers and wing-coverts. ly: All ly retain juv body-feathers which give them a scaly appearance on the upper side. These juv body-feathers are fringed whitish; postjuv ones have no distinct fringes. Juv MaC, MeC, GC and T are fringed whitish (Fig. 64). The breast of ly is usually more prominently spotted dark-brown than in ad, but this is not an infallible ageing criterion.
Fig. 64. ly after partial postjuv moult, 31 August. Most proximal MaC partially postjuv. Rest of wing juv. The well defined whitish fringes on MeC and GC are typical of ly.
Ad: No body-feathers with distinct light fringes present on upperparts. Most northern and central European ad show suspended P-moult during autumn migration which is easily recognized (Fig. 65). They often show pronounced moult limits within T and GC. The GC not moulted during the postbr moult are much more worn than the juv GC (Fig. 65). After a complete postbr moult, ad are recognizable by the fresh plumage and by having MeC, GC and T broadly fringed brownish not narrowly whitish. Ad before the postbr moult and ad which have not started to moult remiges are easily recognized by very worn and bleached P, T and wing-coverts. Resumption of postbreeding moult and extent of prebreeding moult Ad resume a suspended moult of remiges after arrival in the winter quarters or perhaps at stopover sites en route, In spring, it is often impossible to distinguish between remiges renewed before autumn migration and remiges renewed in the wintering area; likewise, it is difficult to judge whether wing-coverts, T and R have been moulted when resuming postbr moult in the winter quarters or later during the prebr
Fig. 65. Ad in suspended postbr moult, 31 August. Before suspension, most
MaC, MeC 2+4-6+8, GC 8-10, CC, T 8-9, P 1-4 and PC 1-3 have been moulted. Easily recognized as ad by the suspended P-moult.
Anthus campestris
67
Fig. 66. 2y after partial prebr moult, 20 April. MaC and MeC prebr. GC 1 juv, 2-10 prebr. T prebr. Rest of wing juv. Juv GC 1, inner PC and CC with welldefined whitish terminal fringes, indicating 2y.
Fig. 69. 2y after eccentric partial prebr moult, 11 May. MaC partially prebr, partially postjuv. MeC and GC prebr. CC juv. Al prebr. T and S 6 prebr. P 5+7 prebr. Rest of wing juv. PC and CC bleached with well-defined whitish terminal fringes. T and GC look older than S 6 and P 5+7, but are not juv.
Fig. 67. 2y after partial prebr moult, 30 April. MaC mostly prebr, some postjuv in the undermost row. MeC and GC prebr. CC and Al prebr. T as well as S 1-2 and 5-6 prebr. PC 1 prebr. Rest of wing juv. Recognizable as 2y by the juv PC with well-defined whitish terminal fringes. T look older than the renewed S, but not as old as the juv S 3^; they may have been renewed early in winter, and are also more exposed. All P have the same pattern of growth bars, confirming 2y.
Fig. 70. Ad after partial prebr moult, 23 April. Postbr and prebr feathers are not distinguishable. Recognizable as ad by the ill-defined brownish terminal fringes on the inner PC. P 1â&#x20AC;&#x201D;5 are probably older than P 6-r9 and may have been renewed before autumn migration (suspended P-moult). S 1â&#x20AC;&#x201D;6 are darker than the innermost P and may have been renewed in the wintering area together with P6-9.
Fig. 68. 2y after eccentric partial prebr moult, 5 May. MaC, MeC and GC prebr. T and S 6 prebr. P 7 prebr. Rest of wing juv. The well-defined whitish terminal fringes of the bleached CC and inner PC are diagnostic of 2y. T look older than S 6 and P 7, but are not juv.
Fig. 71. Ad after partial prebr moult, 13 May. GC 3-4+6+9 probably postbr, rest prebr. The other feathers are difficult to assign to feather generations. Recognizable as ad by the ill-defined buffish terminal fringes on the inner PC.
68
Anthus trivialis
Anthus trivialis Tree Pipit Extent of postjuvenile moult MaC: 20% moult all MaC, 80% leave some, predominantly in the undermost row, unmoulted (N=60). MeC: one third moult part or all MeC, two thirds moult none (N-60). GC: range 0-4, mean 0.3, mode 0, no GC 81.4% (N=775). T: none 87.6%, one 5.7% (mostly T 8 or T 9), two 6.3% (T 8-9), three 0.2% (N=526) (see p. 33). R: none 96.7%, one 3.3% (R 1) (N=520). Birds which renew T and R, but do not moult GC are rare (Fig. 73). The extent of postjuv moult decreases as the autumn migratory season proceeds (Fig. 74). In NW Russia, MeC and the undermost row of MaC are usually only partly moulted. Only five out of 96 ly replaced one or two GC and one had renewed T (Rymkevich 1990). Extent of postbreeding moult Usually whole plumage. Occasionally, interruption of P-moult at an early stage (after P 1-2 have been moulted) occurs (van Hecke 1980, Fig. 21) and may be related to breeding (see section 3.4.1). These birds are likely to complete the postbr moult before migration. Exceptionally, some birds interrupt moult before migration. Such birds may show unmoulted Al 1, Al 1-2 (Fig, 80), PC 9 and/or P 10; one ad was found to have retained S 6 and Al 1, another S 3â&#x20AC;&#x201D;6 and Al 1. This latter bird apparently moulted S 5â&#x20AC;&#x201D;6 of the right wing later during the prebr moult, but not on the left wing (Fig. 84). One migrant on Fair Isle had unmoulted S 4-6 and Al 1-2 (Riddiford 1990) and two out of 33 in Sudan had partially unmoulted S (Nikolaus & Pearson 1991). Comments on ageing after postjuvenile and postbreeding moult Best criteria: Skull pneumatization until at least the end of October (p. 204). Moult limits within MaC, MeC, GC, T and R. Plumage characters sometimes difficult to apply. Fig. 73.Relationships between the number of postjuv GC and the percentage of individuals with renewed T and R in 1 y Anthus trivialis which have completed their postjuv moult.
6
5
4
3
2
1
1
2
3
4
5
6
7
0 10 30 60 90 100%
Fig. 72. Extent of postjuv moult on the wing and tail in ly Anthus trivialis.
ly: 80% of ly show no moult limit within GC. Most of them can be identified by moult limits within MaC or MeC. Postjuv MaC and MeC have darker fringes and feather centres and are less worn than juv ones (Fig. 76 and 77). Very fresh juv GC (usually before mid-August) are not yet worn and bleached and are virtually identical in colour to the postbr GC of ad. ly with a moult limit within GC or T are easily identifiable. Fringes and feather centres of renewed GC and T are darker and contrast with the lighter and already worn fringes of the juv GC and T (Fig. 77 and 78). R cannot be used for ageing unless showing a moult limit (central pair renewed, rest juv)* Ad: Whole plumage fresh, fringes of GC and T not worn, no moult limits within MaC, MeC and T. Note that the innermost three to four GC have somewhat darker fringes than the outer GC and may simulate a moult limit (Fig. 79).
Extent of prebreeding moult: 2y and ad MaC: 32% moult no MaC, 61% part and 7% all (N=137). MeC: 8.7% moult no MeC, 63.1% one to seven and 28.2% all (N=149). 2y moult significantly more MeC (mean 6.0, N=54) than ad (mean 5.2, N=35). GC: range 0-10, mean 4.8, mode 5, no GC 0.5%, all GC 1.6% (N=191). 2y moult significantly more GC (mean 5.0, N=83) than ad (mean 4.4, N=47). T: none 2.1%, one 3.2%, two 2.7%, three 92.0% (N=188). R: none 12.0%, one 58.7% (mostly R 1), two 17.9% (mostly R 1-2), three to six 11.4% (N=184) (see p. 16). P and S: one bird with all T moulted had renewed S 6, one bird S 5^6 (Fig. 84). Ludlow (1966) mentions one bird from Nigeria with P 8 growing on both wings (eccentric P-moult).
Comments on ageing after prebreeding moult Fig. 74. Percentage of ly Anthus trivialis with at least one postjuv GC during autumn (data grouped in five-day periods; the first value includes the period 9-18 August, the last 28 September-17 October).
Moult limits due to the prebr moult occur in ad and 2y. The prebr moult is much more extensive than the postjuv moult. Therefore, three feather generations within GC of 2y are unlikely. Coloration, wear and bleaching of the renewed and unmoulted feathers are sometimes very similar between 2y and ad. Thus, even with experience, ageing every bird in spring is impossible. Usually, P and S of 2y are more bleached and have a more brownish tinge than in ad. The fringes of juv GC are often more worn than those of the postbr GC of ad (cf. Fig. 82 and 83).
Anthus trivialis
69
Fig. 75. Extent of prebr moult on the wing and tail in ad and 2y Anthus trivialis. For differences between ad and 2y see text. Fig. 78. ly after partial postjuv moult, 9 September. MaC postjuv, MeC postjuv. GC 1—7+10 juv, 8—9 postjuv. T 7 juv, 8—9 postjuv. Rest of wing juv. The fringes of the renewed GC and T are less worn and darker than the juv feathers in the corresponding tract.
Fig, 76, 1 y after partial postjuv moult, 16 August. MaC postjuv except one in the undermost row. MeC 1-2 postjuv, 3-8 juv. GC, T and rest of wing juv. The moult limits within MaC and MeC are diagnostic of ly. All GC and T are slightly and uniformly worn.
Fig. 79. Ad after complete postbr moult, 7 September. Whole wing postbr. Whole wing uniformly fresh, MaC, MeC, GC and T almost intact. Note the change in colour within the inner GC which may simulate a moult limit.
Fig. 77. ly after partial postjuv moult, 26 August. MaC postjuv except four juv ones in the undermost row. MeC 4-5+7 juv, rest postjuv. GC 1-8+10 juv, 9 postjuv. T and rest of wing juv. The postjuv GC 9 is fresh, longer and has a darker feather centre than the juv GC. Moult limits within MaC and MeC recognizable by the bleached and worn juv feathers.
Fig, 80. Ad after complete postbr moult, 9 September. Whole wing postbr except Al 1-2. Exceptionally, Al 1—2 remain unmoulted and are heavily bleached. GC 8 is shorter and more worn than the other GC. It may have been lost accidentally and replaced before the ordinary, complete moult.
70
Anthus trivialis Fig. 83. Ad after partial prebr moult, 20 April. MaC partly prebr, partly postbr. MeC 2+8 postbr, rest prebr. GC 1-6+10 postbr, 7-9 prebr. T prebr. Rest of wing postbr. Recognizable as ad because the fringes of the postbr GC are less worn than those of the juv GC in Fig. 82.
Fig. 81. 2y after partial prebr moult, 22 April. MaC mostly postjuv. MeC 1 postjuv, 2-8 prebr. GC 1-4 juv, 5-10 prebr. T prebr. Rest of wing juv. P and S of 2y are usually slightly more bleached and browner than those of ad (cf. Fig. 83). Especially, S 6 contrasts more with the prebr T than in ad.
Fig. 82. 2y after partial prebr moult, 28 April. MaC mostly postjuv. MeC 1-2 postjuv, 3-8 prebr. GC 1-6+10 juv, 7-9 prebr. T prebr. Rest of wing juv. The extent of prebr moult of this 2y bird is similar to that of the ad bird in Fig. 83. Identifiable as 2y because the fringes of the juv GC are more worn than those of the postbr GC in Fig. 83.
Fig. 84. Ad after partial prebr moult, complete postbr moult interrupted, 19 April. MaC mostly prebr. MeC 1-2 prebr, 3-8 postbr. GC 1-7+10 postbr, 8-9 prebr. T 7-8 prebr, 9 postbr. Al 1 not moulted during the last postbr moult, Al 2-3 postbr. S 1-2 postbr, S 3-4 not moulted during the last postbr moult, S 5â&#x20AC;&#x201D;6 prebr. This exceptional bird has neither moulted Al 1 nor S 3-6 during the last postbr moult. During the prebr moult, S 5-6 have been renewed on the right, but not on the left wing (not shown).
Anthus pratensis
71
Anthus pratensis Meadow Pipit Extent of postjuvenile moult MaC: 33% moult all MaC, 67% leave some MaC unmoulted, usually in the undermost row (N=52). MeC: 68% moult none, 24% part and 8% all MeC (N=78). GC: range 0-6, mean 0.5, mode 0, no GC 70.5% (N=373). T: none 71.0%, one 8.9%, two 3.8%, three 16.3% (N=338) (see p. 33). R: none 81.5%, one 16.4% (usually R 1), two 1.5% (usually R 1+6), six 0.6% (N=336) (see p. 34). If no GC are moulted, T and R are rarely renewed (Fig. 86). The extent of postjuv moult is significantly more extensive at the beginning than at the end of the migratory season: before mid-October, 61.3% (N=80) of ly have renewed at least one GC, 60.8% (N=74) at least one T and 39.7% (N=73) at least one R; after mid-October, the respective proportions are 20.7% (N=290), 20.3% (N=261) and 12.7% (N=260). In SW Niedersachsen, at least 52% of actively moulting ly renewed one or more T and 40% one or more R (N=151, Hotker in Glutz & Bauer 1985). This corresponds to the values of the first part of the migratory season in Switzerland. On the island of Mellum (North Sea), 18.3% of ly moult at least one R and only a few ly one or more T (N=60, Henle 1983). Svensson (1992) noted that early-hatched and southern populations are more likely to moult MeC, GC and T than late-hatched and northern populations.
Fig. 85. Extent of postjuv moult on the wing and tail in ly Anthus pratensis,
Extent of prebreeding moult: 2y and ad MaC: not or only partially moulted (N=36). MeC: 75% moult none, 25% one to all MeC (N=72). GC: range 0-5, mean 0.8, mode 0, no GC 49.3% (N=75). T: none 8.1%, one 20.3%, two 14.9%, three 56.8% (N=74) (see p. 15). R: none 32.9%, one 48.6% (usually Rl), two 5.7%, three 2.9%, four 2.9%, five 2.9%, six 4.3% (N=70) (see p. 16).
Extent of postbreeding moult Whole plumage. Rarely, individual PC and Al may be retained. Comments on ageing after postjuvenile and postbreeding moult Best criteria: Skull pneumatization until the end of September (p. 204). ly usually identifiable by moult limits within MaC, MeC and GC ly: ly without a moult limit within GC (68%) are usually recognizable by moult limits within MeC or MaC (Fig. 88 and 89). ly with moult limits within GC are easily identifiable. Postjuv GC contrast with juv GC in their dark, olive-brown and intact fringe (Fig. 89 and 90). Also check for moult limits within T and between postjuv T and juv S 6. Ad: All MaC, MeC, GC and T fresh. The fringes of GC have a more olive tinge and contrast more with the dark feather centre than in ly, although there is some individual variation. The difference in colour between T and S 6 is only slight.
Fig. 86. Relationships between the number of postjuv GC and the percentage of individuals with renewed T and R in ly Anthus pratensis which have completed their postjuv moult.
Fig. 87. Extent of prebr moult on the wing and tail in ad and 2y Anthus pratensis.
Comments on ageing after prebreeding moult Moult limits due to the prebr moult occur in ad and 2y. Since coloration and wear of the feather generations acquired before the prebr moult are very similar in 2y and ad, ageing in spring is only possible in a few cases and by an experienced observer. Usually, P, S and the fringes of unmoulted GC are more bleached in 2y than in ad.
72
Anthus pratensis
Fig. 88. ly after partial postjuv moult, 3 October. MaC partly juv, partly postjuv. MeC juv. GC, T and rest of wing juv. Recognizable as ly by the mixed MaC. The postjuv MaC have fresher fringes and darker feather centres than the juv MaC. GC and T slightly and uniformly worn. The fringes of juv GC are usually whitish and gradually fade into the dark colour of the feather centres.
Fig. 91. Ad after complete postbr moult, 20 October. Whole wing postbr. MaC, MeC, GC and T virtually intact. Fringes of GC have a more olive tinge and contrast slightly more with the dark feather centres than in juv GC.
Fig. 89. ly after partial postjuv moult, 19 October. MaC postjuv. MeC 1-4 juv, 5-8 postjuv. GC 1â&#x20AC;&#x201D;8+10 juv, 9 postjuv. T 7â&#x20AC;&#x201D;9 postjuv. Rest of wing juv. Easily recognizable as ly by the postjuv GC 9 which is darker, fringed more olive and less worn than the juv GC. Moult limit between T and S 6.
Fig. 92. 2y after partial prebr moult, 14 April. MaC partly juv, partly postjuv, partly prebr. MeC 1-4+8 juv or postjuv, 5-7 prebr. GC 1-7+10 juv, 8-9 prebr. T 7+9 prebr, 8 probably postjuv. Rest of wing juv. P, S and the fringes of the juv GC are more bleached than in ad.
Fig. 90. ly after partial postjuv moult, 6 October. MaC and MeC postjuv. GC 1-6 juv, 7-10 postjuv. T postjuv. Rest of wing juv. The postjuv GC are less worn and contrast with the juv GC in their broad olive-brown fringes. Postjuv T darker than juv S 6.
Fig. 93. Ad after partial prebr moult, 7 April. MaC mostly postbr. MeC postbr. GC 1â&#x20AC;&#x201D;8+10 postbr, 9 prebr. T prebr. Rest of wing postbr. P and S slightly darker and fringes of postbr GC slightly less bleached than in 2y.
Anthus spinoletta spinoletta
73
Anthus spinoletta spinoletta Water Pipit Extent of postjuvenile moult MaC: about 50% moult all and 50% retain some juv MaC in the undermost row. MeC: 50% moult none, 45% part, 5% all MeC. GC: range 0-2, mean 0.5, mode 0, no GC 59.4% (N=160). T: none 71.3%, one 23.1%, two 3-5%, three 2.1% (N=143) (see p. 33). R: none 95.8%, one 4.2% (R1)(N=144). Most ly which renew T and all ly which renew R moult at least one GC (Fig. 95). During the first part of the autumn migration season (until the end of September), 50% of ly had renewed one to two GC (N=l 11) and 34% (N=97) one to three T; thereafter, the percentages were significantly lower (18% and 18%, respectively, N=49).
Fig. 94. Extent of postjuv moult on the wing and tail in ly Anthus s. spinoletta,
Whole plumage. Exceptionally, Al 1 may remain unmoulted (one out of 49 ad).
N=102) than ad (mean 1.7, N=59, difference not significant). T: one 1.3%, two 5.8%, three 92.9% (N=224). Significantly more 2y moult all T (96.0%, N=101) than ad (85.2%, N=54). R: none 4.5%, one 87.9% (R 1), two 7.6% (usually R 1+2) (N=224) (see p. 16). S: two birds with all T moulted had also renewed S 6 on one wing. This was also observed in one bird by Herremans (1987).
Comments on ageing after postjuvenile and postbreeding moult
The extent of the prebr moult of spring migrants in Belgium is very similar to our data (Herremans 1987).
Extent of postbreeding moult
Best criteria: Skull pneumatization until at least November (p. 204). Moult limits within MeC, GC and T. Plumage criteria sometimes difficult to apply and not always conclusive. ly: It is important to realize that the inner juv GC as well as the inner postbr GC of ad are differently coloured than the outer GC of the same feather generation and may simulate a moult limit (Fig. 97 and 100). Furthermore, very fresh juv GC (usually birds in juvenile plumage) have brownish fringes like the GC of ad after postbr moult (cf. Fig. 97 and 100). Juv GC, however, bleach more rapidly than ad GC. In order to recognize moult limits within GC (40% of ly), check especially for differences in colour of the feather centre and wear, ly without moult limits in GC often have a moult limit within MeC (Fig. 98). Ad: No moult limits within MeC, GC and T. Fringes of GC contrast more strongly with the dark feather centres than in ly. Fringes on outer GC are usually brownish or reddish-brown, not whitish, although individual differences and bleaching may give them a more juv appearance. Fig. 96. Extent of prebr moult on the wing and tail in ad and 2y Anthus s. spinoletta. For differences between ad and 2y see text.
Extent of prebreeding moult: 2y and ad MaC: not moulted (N=35). MeC: 55% moult one to six central MeC, 45% none (N=35). At least one MeC is significantly more often moulted by 2y (68%, N=19) than byad(27°/o,N=ll). GC: range 0â&#x20AC;&#x201D;6, mean 1,8, mode 2, no GC 7.1%, GC 10 is moulted by 4.9% only (N=224). 2y birds moult slightly more GC (mean 1.9,
Fig. 95. Relationships between the number of postjuv GC and the percentage of individuals with renewed T and R in ly Anthus s, spinoletta which have completed their postjuv moult.
Comments on ageing after prebreeding moult Ageing in spring is very difficult, even by experienced observers. Moult limits due to the prebr moult occur in both 2y and ad. The prebr moult is much more extensive than the postjuv moult. Therefore, three feather generations within GC (Fig. 102) are very rare (0.5%). Usually, S and P of ad are slightly darker and contrast slightly less with the prebr T than in 2y. Postbr GC of ad are usually slightly less bleached than the juv GC of 2y. Only birds with two moult limits within GC (0.5%) are safely identifiable as 2y (Fig. 102).
74
Anthus spinoletta spinoletta
Fig. 97* ly in juvenile plumage, 1 August. Whole wing juv. Note that the fringes of the juv GC 8â&#x20AC;&#x201D;9 are browner than those of the adjacent GC and may simulate a moult limit.
Fig. 100. Ad after complete postbr moult, 5 October. Whole wing postbr. Fringes of GC contrast strongly with the feather centres. Fringes of outer GC brownish, not whitish. Note that the four innermost GC have darker fringes than the others which may simulate a moult limit.
Fig. 98. ly after partial postjuv moult, 1 October. MaC postjuv, a few outermost juv. MeC 1-3+8 juv, 4-7 postjuv. GC 1â&#x20AC;&#x201D;8+10 juv, 9 postjuv. T and rest of wing juv, The moult limits within MeC and GC are diagnostic of ly. The renewed MeC and GC 9 have darker black feather centres and totally intact, browner fringes than the juv GC and MeC which have lighter feather centres and worn margins.
Fig. 101. 2y after partial prebr moult, 7 April. MaC postjuv. MeC 3+8 prebr, 1-2+4-7 postjuv. GC 1-7+10 juv, 8-9 prebr. T prebr. Rest of wing juv. Compared with the corresponding postbr feathers of ad (cf. Fig. 103), the juv GC, S and P are more bleached, especially when comparing S 6 with the dark prebr T.
Fig. 99. ly after partial postjuv moult, 10 October. MaC and MeC postjuv. GC 1-7+10 juv, 8-9 postjuv. T 7-9 postjuv. Rest of wing juv. The renewed GC have darker feather centres than juv GC and clearly defined fringes. A conspicuous moult limit is visible between the postjuv T and the juv S.
Fig. 102. 2y after partial prebr moult, 14 April. MaC postjuv. MeC postjuv. GC 1â&#x20AC;&#x201D;7 juv, 8 postjuv, 9 prebr, 10 juv or postjuv. Rest of wing juv. Identifiable as 2y by the three feather generations within the GC. The postjuv GC 8 is darker, especially near the tip, and less worn than the juv GC 7, but not as dark and intact as the prebr GC 9.
Anthus spinoletta spinoletta
75
Fig. 104. Ad after partial prebr moult, 6 April. MaC mostly postbr. MeC 6+8 prebr, rest postbr. GC 1—4 postbr, 5—10 prebr. T prebr. Rest of wing postbr. Rare case of an extensive prebr moult.
Fig. 103. Ad after partial prebr moult, 17 April. MaC postbr. MeC 5+6 prebr, rest postbr. GC 1—7+10 postbr, 8—9 prebr. T prebr. Rest of wing postbr. The postbr GC have darker feather centres than the juv GC of 2y birds (cf. Fig. 101 and 102). S and P are also darker than in 2y. S 6 contrasts less with the prebr T than in 2y.
76
Mo tacilia fla va
Motacillaflava Yellow Wagtail Extent of postjuvenile moult MaC and MeC: usually all. In about 10% (almost exclusively ly without renewed GC), individual MaC of the undermost row and MeC (rarely all) may remain unmoulted (N=79). GC: range 0-10, mean 1.9, mode 0, no GC 48.2%, all GC 0.7% (N=876). CC: 1.6%. Al: none 97.9%, one 2.1% (N=610). T: none 90.6%, one 4.2%, two 4.7%, three 0.5% (N=832) (see p. 33). R: none 90.1%, one 5.2% (usually R 1), two 2.9% (often R 1+6), three to five 1.8% (N=829) (seep. 34). The extent of postjuv moult is correlated among GC, CC, Al, T and R (Fig. 106). The extent of postjuv moult decreases as the autumn migratory season proceeds (Fig. 107). Scandinavian birds perform a considerably less extensive postjuv moult than that recorded in NW Russia, Switzerland and England: less than 5% moult at least one GC and only a small proportion moult MeC (Svensson 1992). In NW Russia (Rymkevich 1990), 50% moult MeC and 28% one to four GC (mean of all ly 0.5, N=133). In England (Hereward 1979), 52% of ly were recorded with at least one renewed GC and the frequency distribution of the number of moulted GC is similar to that in Switzerland, though the percentage of birds with all GC moulted (6.7%) is higher than in Switzerland (0.7%). In England, the number of GC moulted decreases during late summer, apparently due to the later appearance of late-hatched birds moulting fewer GC (Hereward 1979). In E Germany (Dittberner & Dittberner 1987), about 30% of ly were recorded as moulting a few or all R, some GC and some T; strangely, moult of PC was recorded (no details given) and one bird, apparently aged as ly, had P 1—2 growing.
Fig. 106. Relationships between the number of postjuv GC and the percentage of individuals with renewed CC, Al, T and R in ly Motacillaflava which have completed their postjuv moult.
Fig. 107. Mean number of postjuv GC during autumn of ly Motacilla flava which have completed the postjuv moult (data grouped in five-day periods; the first value includes the period 14-28 August, the last 3— 17 October).
Fig. 105. Extent of postjuv moult on the wing and tail in ly Motacillaflava,
Extent of postbreeding moult Whole plumage. Moult during postbreeding movements or the beginning of autumn migration was observed in Great Britain and Germany (Hereward 1979, Dittberner & Dittberner 1987). Exceptionally, moult interruption occurs. Among 98 ad caught on Col de Bretolet, one had S 6, Al 2-3, GC 10, MeC and some MaC (Fig. 118) and two birds Al 1 unmoulted (Fig. 117), the Al being among the last feathers on the wing to be renewed (Spina & Massi 1992). In NE Spain, an ad which retained S 5-6, Al 1, some MeC and MaC was observed (Aymf & Jaume 1992). Moult interruption during the first stages of P-mouIt may occur as well (Herroelen 1982a), but these birds are likely to complete moult before migration. Comments on ageing after postjuvenile and postbreeding moult Best criteria: Skull pneumatization until at least the end of October (p. 204). Most ly recognizable by moult limits within GC, MeC or between MeC and MaC. A few ly with all GC moulted are more difficult to separate from ad on plumage characters alone. ly: 51% show a moult limit within GC which is usually conspicuous (Fig. 111-115). The juv GC, especially the central ones (GC 4-7), have a well-defined white fringe. Postjuv GC have an ill-defined yellowish, greenish or light greyish-brown fringe, varying individually in colour. Note that juv, postjuv and postbr GC 8—10 have slightly differently coloured fringes than the other GC of the same feather generation (Fig. 109, 110 and 117) and may simulate a moult limit. Therefore, always check for differences in wear and also in the colour of the feather centres, ly with no GC moulted (48%) are often recognizable by having a moult limit within MeC (Fig. 109) or else by the white fringes on all GC and the contrast between postjuv MeC and juv GC (Fig. 110). ly with all GC moulted (0.7%) are difficult to distinguish from ad and may be recognized by moult limits within Al, T and R. Juv and postjuv T and R can be distinguished by differences in wear rather than by differences in colour. For instance, T 7 is always darker than T 8—9 of the same feather generation and is fringed white. Ad: Fringes of all GC without white, fading into the dark feather centres. No moult limits within T, R and Al (Fig. 116 and 117). The few birds retaining individual feathers during the postbr moult (Fig. 117 and 118) are easily identified as ad by the strongly worn and bleached feathers. Extent of prebreeding moult: 2y and ad In spring, the wing-coverts are often difficult to assign to the correct feather generation. Only a few birds migrate through Europe with fresh
Motacilla and intact wing-coverts, T and R (Fig. 122). Most birds show different stages of wear. Especially the exposed GC 8-9 and T 8-9 are often worn to such an extent that it is not possible to determine whether they have been renewed very early during the prebr moult or whether they are juv or postbr (cf. Roselaar in Cramp 1988). The feathers of ad are easier to assign since their plumage is composed of only two feather generations (postbr and prebr). In some ad, the outer GC are definitely postbr, the central GC prebr and the inner GC are already worn and also prebr, since they are not so bleached as the outer postbr GC (Fig. 123). In such birds, T 8—9 are usually more worn than T 7 and R. These observations suggest that the prebr moult of many Yellow Wagtails extends over a long period or is divided into two phases. Accordingly, the innermost GC, some MaC and MeC and T 8—9 are likely to be moulted during the first phase, and the central and outer GC, the remaining MaC and MeC, T 7 and all R during the second phase. A long-lasting prebr moult, lasting about 90 days, is confirmed from Nigeria (Wood 1976). In Kenya, the body-feathers are moulted in two distinct phases (Pearson & Backhurst 1973, DJ. Pearson in lift.). During a first phase in November—early December, many feathers of the head, throat and mantle are renewed. During a second phase, lasting about 60 days, in January—March the actual prebr moult takes place and the head feathers are renewed again. In Italy, 10.6% of the birds caught during spring migration (N=871) still showed growing feathers on head and neck (Serra 1992). For the reasons given above, the following data on the extent of prebr moult are subject to reservations. The percentage of inner GC, T and perhaps R moulted during the prebr moult might be lower than given here. Our data, however, agree well with those of Wood (1976) and Serra (1992), who found about the same number of GC moulted and also suggest a moult of all T and R. MaC: 47.7% moult all, 43.0% part and 9.3% no MaC (N=107). MeC: 52.5% moult all, 46.8% part of the MeC. Only one bird did not moult any MeC (N=l4l). Ad and 2y moult similar numbers of MeC. GC: range 4-10, mean 6.7, mode 6, all GC 6.2% (N=145). 2y birds moult significantly more GC (mean 7.1, N=56) than ad (mean 6.4, N=34). CC: 2.2%. Al: none 94.7%, one 5.3% (N= 94). T: one 6.9% (T 7), two 2.1% (T 7+9), three 91% (N= 145). R: probably all birds renew all R (N=131). S: one bird with all R, T and GC as well as Al 1 and CC moulted had also renewed S 6 on both wings (Fig. 121).
flava
77
Fig, 108. Extent of prebr moult on the wing and tail in ad and 2y Motacilla flava. For differences between ad and 2y see text.
Fig. 109. ly after partial postjuv moult, 1 September. MaC postjuv, except some outermost juv. MeC 1-5 postjuv, 6-8 juv. GC, T and rest of wing juv. Recognizable as ly by the conspicuous moult limit within MeC. The juv GC have well-defined white fringes which are often narrow on GC 8-10 and may simulate a moult limit.
Comments on ageing after prebreeding moult Ageing in spring is difficult and not always possible for every bird. Moult limits due to the prebr moult occur in all 2y and ad. Since the prebr moult is more extensive than the postjuv moult, prebr GC usually directly adjoin the juv GC in 2y. Three feather generations within GC are exceptional (one bird out of 65, but 16.5% out of 85 in the sample of Serra 1992). If the GC which have not been moulted during the prebr moult are not heavily worn, well-defined white fringes (juv GC) are diagnositc of 2y (Fig. 119). Ill-defined greyish, yellowish or greenish fringes (postbr GC) indicate ad (Fig. 122 and 123). Many (but not all, see Fig. 120) 2y also have well-defined white fringes on Al 1 and CC (Fig. 119). Ad usually have ill-defined, not white, fringes. Advanced wear may prohibit use of these criteria from the end of April. Then, 2y may usually be distinguished from ad by having more heavily worn and bleached P, S and those GC not moulted during the prebr moult (Fig. 120). The same ageing criteria as given above have recently been proposed by Serra (1992). Fig. 110. ly after partial postjuv moult, 18 September. MaC and MeC postjuv, GC juv. T 7+9 juv, 8 postjuv. Rest of wing juv. Exceptional case of a ly which moulted a T without having renewed any GC. Recognizable as ly by the white fringes on all GC and the contrast between postjuv MeC and juv GC.
78
Motacilla flava Fig. 111. 1 y after partial postjuv moult, 8 September. MaC and MeC postjuv. GC 1-7+10 juv, 8-9 postjuv. T and rest of wingjuv. Conspicuous moult limit within GC. The renewed GC have illdefined greenish fringes.
Fig. 112. ly after partial postjuv moult, 7 September, MaC and MeC postjuv. GC 1-4+10 juv, 5-9 postjuv. T and rest of wing juv. Conspicuous moult limit within GC. GC 10 remained unmoulted although five GC have been renewed.
Fig. 115- ly after partial postjuv moult, 6 September. MaC and MeC postjuv. GC 1 juv, 2-10 postjuv. CC postjuv. Al 1 postjuv, 2-3 juv. T 7 juv, 8-9 postjuv. Rest of wing juv. GC 1, the only juv one, contrasts with the other GC in having a well-defined white fringe. The renewed T 8-9 are recognizable as postjuv by their illdefined greenish fringes. T 7 is always fringed white, but slightly more worn than the other T.
Fig. 113. 1 y after partial postjuv moult, 11 September. MaC and MeC postjuv. GC 1â&#x20AC;&#x201D;7 juv, 8â&#x20AC;&#x201D;10 postjuv. T 7+9 juv, 8 postjuv. Rest of wing juv. Conspicuous moult limit within GC. GC 10 is also moulted. Fig. 116. Ad $ after complete postbr moult, 18 September. Whole wing fresh. Fringes of all GC ill-defined and not white. No moult limit within T.
Fig. 114. 1 y after partial postjuv moult, 8 September. MaC and MeC postjuv. GC 1+5-8+10 juv, 2-4+9 postjuv. T and rest of wing juv. Irregularities within the sequence of GCmoult occur more frequently than in other species.
Fig. 117. Ad 9 after complete postbr moult, 4 October. Whole wing postbr, except Al 1 and MeCl. Exceptionally, Al 1 and MeC 1 remained unmoulted. Fringes of all GC ill-defined and not white. Note that the fringes of GC 8-10 are slightly darker than in the other GC and may simulate a moult limit.
Motacilla
Fig. 118. Ad 9 after postbr moult interrupted at S 6, 24 September. Most MaC, all MeC, GC 10, Al 2-3 and S 6 remained unmoulted. These feathers are heavily worn and bleached. Fig. 119. 2y 9 after partial prebr moult, 26 April. MaC mostly prebr. MeC 1 postjuv, 2-8 prebr. GC 1-4 juv, 5-10 prebr. T prebr. Rest of wing juv. Recognizable as 2y by the juv GC which are heavily bleached and, like A l l and CC, have well-defined white fringes.
flava
79
Fig. 121. Probably 2y 6 after partial prebr moult, 23 April. MaC, MeC, GC, CC, Al 1, T and S 6 prebr. Rest of wing probably juv. Exceptional case of an extensive prebr moult which included even S 6. The age cannot be told with certainty. The bleached S and P, the Al 2 fringed white and the worn outer PC suggest a 2y.
Fig. 122. Ad c3 after partial prebr moult, 2 May. MaC and MeC prebr. GC 1-2 postbr, 3-10 prebr. T prebr. Rest of wing postbr. GC 1-2 are moderately worn and have illdefined greyish, not white fringes. The same holds for the fringes of Al and CC. These characters indicate the ad. All prebr wing-coverts are similarly fresh.
Fig. 120. 2y 8 after partial prebr moult, 24 April. MaC and MeC prebr. GC 1-3 juv, 4-10 prebr. T prebr. Rest of wing juv. Juv GC heavily worn and their white fringes almost completely worn off. Juv CC and Al 1 without white fringes.
Fig. 123. Ad 8 after partial prebr moult, 22 April. MaC mostly prebr. MeC 1 postbr, 2-8 prebr. GC 1-4 postbr, 5-10 prebr. T prebr. Rest of wing postbr. P 6 has probably been renewed following an accident (right wing only). The postbr GC 1-4, CC and Al still show ill-defined greyish fringes, which distinguish them from the corresponding juv feathers and indicate the ad. GC 7-9 and T 8-9 are more heavily worn than the other prebr GC 5-6 and T 7; they have probably been renewed during the first part of the prebr moult and considerably earlier than GC 5-6 and T 8-9.
80
Motacilla cinerea
Motacilla cinerea Grey Wagtail Extent of postjuvenile moult MaC and MeC: usually all. 1 y with no or few moulted GC may retain some juv MeC. GC: range 0-10, mean 3.8, mode 0, no GC 18.7.%, all GC 1.1% (N=91). CC: 17.4%. Al: none 71.0%, one 24.6%, two 4.3% (N=69). T: none 36.5%, one 10.8%, two 16.2%, three 36.5% (N=74) (see p. 33). R: none 42.7%, one 10.7% (usually R 1), two 13.3% (usually R 1+6), three to five 17.3%, six 16.0% (N=75) (see p. 34). CC and Al 1 may be renewed when at least three, T and R when at least two GC are moulted, ly with at least seven GC moulted have all T and usually three to six R renewed. In Switzerland, the extent of postjuv moult decreases as the autumn migratory season proceeds: before the end of September, 4.6 GC are moulted on average (10 and 90 percentiles 1-8, N=56), and after that only 2.4 (0-6, N=29). In Belgium, the extent of postjuv moult is very similar and also decreases during autumn migration; four out of 308 ly were found to have renewed PC 1 (Herremans 1988a). Extent of postbreeding moult Whole plumage.
Fig. 124. Extent of postjuv moult on the wing and tail in ly Motacilla cinerea.
Extent of prebreeding moult: 2y and ad MaC: three quarters of 2y moult none, one quarter moult the proximal MaC only (N=21). MeC: usually not moulted. One 2y had a single new MeC (N=32). GC: range 0-2, mean 0.5, mode 0, no GC 68.2% (N=44). GC are often moulted out of the normal sequence. T: none 22.7%, one 20.5%, two 25.0%, three 31.8% (N=44) (see p. 15). R: none 57.5%, one 15.0% (usually R 1), two 17.5% (usually R 1+6), three to five 7.5%, six 2.5% (N=40) (see p. 16).
Comments on ageing after postjuvenile and postbreeding moult Best criteria: Skull pneumatization until at least mid-winter (p. 204). Moult limit within GC diagnostic of most ly, otherwise check for moult limits within Al, T or between T and S. ly: 80% show a moult limit within GC which is easily recognizable by a difference in colour of the fringes if situated within the central GC. Juv GC 4â&#x20AC;&#x201D;8 have a whitish, postjuv GC 4â&#x20AC;&#x201D;8 a greyish fringe (Fig. 128), and are often longer (Fig. 129). The feather centres of juv GC are less dark than in postjuv GC (Fig. 128). This is important for recognizing moult limits within outer GC where the colour of the fringes is less decisive. Note that juv, postjuv and postbr GC 9 and 10 are slightly greyer than the other GC of the same feather generation and may simulate a moult limit (cf. Fig. 126, 127 and 130). Also check for moult limits within T. 1 y with no GC moulted (19%) are recognizable by the slight difference in colour between the renewed MeC and the juv GC (Fig. 127). ly with all GC renewed (1.1%) are difficult to separate from ad. Often, a renewed CC, a moult limit within Al or T or between T and S 6 is diagnostic.
Fig. 125- Extent of prebr moult on the wing and tail in ad and 2y Motacilla cinerea.
Ad: No moult limits within GC, T and Al. S 6 and T 7 have the same black colour (Fig. 130). Note that GC 9 and 10 are slightly greyer than the adjacent GC. Comments on ageing after prebreeding moult Ageing spring birds is difficult. Moult limits due to the prebr moult occur in 2y and ad. Since the prebr moult is usually less extensive than the postjuv moult (68% without any prebr GC), 2y are often recognizable, as in autumn, by moult limits within GC due to the postjuv moult (Fig. 132 and 133). Some 2y have three feather generations within GC, thus showing two moult limits (Fig. 131). Birds showing no moult limit or only a moult limit due to the prebr moult within GC (all ad, some 2y) are difficult to age. In ad, P and S are usually slightly darker than in 2y and contrast less with T (Fig. 134).
Motacilla cinerea
Fig. 126. ly in juv plumage, 3 August. One central MaC postjuv. Rest of wing juv. GC 1-8 fringed whitish. GC 9 and 10 are greyer than the others and may simulate a moult limit. No marked contrast between MeC and GC.
Fig. 127. ly after partial postjuv moult, 21 September. MaC and MeC postjuv. GC juv. T and rest of wing juv. Recognizable as ly by the postjuv MeC being darker blackish-grey than the juv GC.
Fig. 128. ly after partial postjuv moult, 17 September. MaC and MeC postjuv. GC 1—6 juv, 7—10 postjuv. T postjuv. Rest of wing juv. Conspicuous moult limit within GC. The juv GC 4—6 (but not 1—3) have whitish fringes and brownish-grey feather centres, the inner postjuv GC greyish fringes and blackish feather centres. The renewed T contrast with the juv S in their black colour.
81
Fig. 129. ly after partial postjuv moult, 19 September. MaC and MeC postjuv. GC 1-7+10 juv, 8-9 postjuv. T 7+9 juv, 8 postjuv. Rest of wing juv. The postjuv GC 8-9 contrast with the adjacent juv GC in their darker feather centres and their length. Note that the slight difference in colour among the two renewed GC corresponds to that in ad (cf. Fig. 130).
Fig. 130. Ad after complete postbr moult, 29 September. Whole wing postbr. S as dark as T. Difference in colour between MeC and GC less than in those ly with no renewed GC (cf. Fig. 127). The two innermost GC are slightly greyer than the others and may simulate a moult limit.
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Motacilla cinerea Fig. 133. 2y after partial prebr moult, 17 April, MaC mostly postjuv. MeC postjuv. GC 1â&#x20AC;&#x201D;7 juv, 8-10 postjuv. T 7+9 prebr, 8 juv or postjuv. Rest of wing juv. As in Fig. 132, this bird moulted only a few MaC during the prebr moult. Although the fringes are largely abraded, the moult limit due to the postjuv moult is still recognizable.
Fig. 131. 2y after partial prebr moult, 15 April. MaC partly prebr, partly postjuv. MeC postjuv. GC 1-6 juv, 7+9 prebr, 8+10 postjuv. T prebr. Rest of wing juv. Recognizable as 2y by the three feather generations within GC. The juv GC are brownish and the inner ones (GC 4-6) fringed whitish. The postjuv GC 8 shows a colour of the feather centre intermediate between that of the juv GC 1-6 and the prebr GC 7+9.
Fig, 132. 2y after partial prebr moult, 17 April. MaC mostly postjuv. MeC 5 prebr, rest postjuv. GC 1â&#x20AC;&#x201D;3 juv, 4â&#x20AC;&#x201D;10 postjuv. T prebr. Rest of wing juv, This bird moulted no wing-coverts during the prebr moult, except some inner MaC and MeC 5. Within the GC, which are all worn, the moult limit due to the postjuv moult is easily recognizable.
Fig. 134. Ad after partial prebr moult, 5 April. MaC partly prebr, partly postbr. MeC, GC, T and rest of wing postbr. Birds having no moult limit, or one due only to the prebr moult, are difficult to age. The postbr GC of ad are darker and fringed greyish, not whitish, P and S are darker than in 2y and hardly contrast with the renewed T.
Motacilla alba alba
83
Motacilla alba alba White Wagtail Extent of postjuvenile moult MaC and MeC: usually all. ly with no renewed GC may retain some juv MeC. GC: range 0-10, mean 5.3, mode 7, no GC 10.6%, all GC 4.5% (N=358). CC: 9.7%. Al: none 93.5%, one 6.5% (N=339). T: none 36.9%, one 15.6%, two 17.3%, three 30.3% (N=347) (see p. 33). R: none 48.2%, one 15,2% (usually R 1), two 18.4% (usually R 1+6), three 7.3%, four 4.4%, five 2.0%, six 4.4% (N=342) (see p. 34). P and S: one bird from S Italy (on both wings P 8—9 postjuv, PC juv, GC 2-10, T and R postjuv; Winkler & Jenni 1987) and one bird from Switzerland (P 6 postjuv on one wing only, PC juv, GC 1—10, Tand R postjuv) showed eccentric P-moult. Another bird from Switzerland had renewed S 5—6 on the left wing and S 6 on the right wing (GC 1—10, T and R postjuv on both wings). The extent of postjuv moult is correlated among GC, CC, Al, T and R (Fig. 136). CC and Al 1 may be renewed when at least six GC are moulted. When more than six GC are moulted, over 50% of ly moult at least one T and R. The extent of postjuv moult decreases as the autumn migratory season proceeds (Fig. 137). As observations from the Netherlands (Jukema & Rijpma 1984), NW Russia (Rymkevich 1990) and England (M. a. yarrellii, Baggott 1970, Broom et ai 1976) show, the postjuv moult is faster and less extensive in late-hatched than in early-hatched ly. In England, most ly renew seven to eight GC and all T and R, but late-hatched ly less than seven GC or none and only some or no T and R (Baggott 1970, Broom et aL 1976); furthermore, $ replace more GC than 9 (Baggott 1970). In NW Russia, usually all MeC, four to ten GC (mean 5.6, all GC 9-1%, N=166), rarely T 8 or T 8-9 and one R are moulted, but never CC and Al. Thus, the moult of T, R, CC and Al in NW Russia is less Fig. 136. Relationships between the number of postjuv GC and the percentage of individuals with renewed CC, Al, T and R in ly Motacilla alba which have completed their postjuv moult.
Fig. 137. Mean number of postjuv GC during autumn of ly Motacilla alba which have completed the postjuv moult (data grouped in five-day periods; the first value includes the period 8—27 September).
Fig. 135- Extent of postjuv moult on the wing and tail in ly Motacilla alba. extensive than in Switzerland, the Netherlands and England, and even considerably less in Scandinavia where most ly renew only one or a few GC(Svensson 1992).
Extent of postbreeding moult Whole plumage. Exceptionally Al 1 may remain unmoulted (one bird). Comments on ageing after postjuvenile and postbreeding moult Best criteria: Skull pneumatization until mid-October (p. 204). Moult limits within GC, between GC and MeC and between T and S 6. ly: 85% show a moult limit within GC which is most conspicuous if situated in the area of GC 4—8 (Fig. 142) and usually more distinct in 6 than in ? . Compared with juv GC, postjuv GC have darker feather centres, are less worn, and have better defined fringes which form a more distinct step between the inner and outer web, especially on GC 4—8. ly with no GC moulted (11%) are recognizable by the difference in colour between the juv GC and the postjuv MeC (Fig. 139 and 141). ly with all GC renewed (5%) usually moult all T and show a contrast between the black base of the postjuv T 7 and the more greyish base of the juv S 6 (Fig. 145). Since such birds usually also moult CC and Al 1, moult limits within Al and between CC and PC may also be helpful. As ly may renew all R, they can be used for ageing only if they show a distinct regular moult limit. Ad: No moult limits between GC and MeC, within GC, Al and between CC and PC. Difference in colour between the bases of T 7 and S 6 only slight.
Fig. 138. Extent of prebr moult on the wing and tail in ad and 2y Motacilla alba. For differences between ad and 2v see text.
84
Motadlla alba alba
Extent of prebreeding moult: 2y and ad MaC: not or only partially moulted (N=63). MeC: 6% moult all, 81% part (mostly three to four central) and 13% moult no MeC (N=63). 2y and ad moult similar numbers of MeC. GC: range 0-7, mean 3.4, mode 3, no GC 6% (N=124). 2y moult slightly more GC (mean 3.5, N=81) than ad (mean 3.0, N=42, difference not significant). T: none 12%, one 38% (usually T 8), two 17%, three 33% (N=123) (seep. 15). 2y moult slightly more T (mean 1.8, N=81) than ad (mean 1.5, N=42, difference not significant). R: none 49%, one 24% (usually R 1), two 24% (usually R 1+6), three to four 3% (N= 117) (see p. 16). Comments on ageing after the prebreeding moult in spring, ageing is difficult ana in some cases impossible. Moult limits due to the prebr moult occur in 2y and ad. During the prebr moult, more T, but fewer R and considerably fewer GC are moulted than during the postjuv moult. Therefore, moult limits between juv and postjuv GC are still retained in many 2y. Such birds show three feather generations within GC, i.e. from outside to inside juv, postjuv and prebr GC. Only 2y showing three feather generations within GC (54.5%) are safely determinable (Fig. 148 and 149). 2y with only one moult limit within GC, as most ad have, are difficult to age; these are either birds which did not renew any GC during the prebr moult (3.9%) or birds which renewed more GC during the prebr moult than during the postjuv moult (41.6%, Fig. 150). They may often be recognized as 2y by the juv GC being more bleached than the postjuv GC of ad. 2y which moulted all GC during the postjuv moult (Fig. 151) are even more difficult to distinguish from ad. With much experience, they may be recognized by their more heavily bleached and browner P and S. In ad, P and S are usually more blackish and PC and Al have often more distinct white fringes (cf. Fig. 149 and 152). Fig. 139. ly (3 after partial postjuv moult, 13 October. MaC and MeC postjuv. GC, T and rest of wing juv. A S with broader fringed GC than in 9 (cf.Fig. 141). All GC similarly worn with illdefined fringes merging gradually into the greyish-brown feather centres. Again, the contrast between postjuv MeC and juv GC is diagnostic of ly.
Fig. 140. ly after partial postjuv moult, 13 October. MaC and MeC postjuv. GC 1â&#x20AC;&#x201D;8+10 juv, 9 postjuv. T and rest of wing juv. The postjuv GC 9 contrasts with the juv GC. It has a darker feather centre and is less worn.
Fig. 141. ly after partial postjuv moult, 13 October. MaC and MeC postjuv. GC, T and rest of wing juv. GC all similarly worn with greyish-brown feather centres. Since the fringes of the GC are narrow, this bird is probably a 9. Recognizable as ly by the contrast between postjuv MeC and juv GC which is slightly more pronounced than in ad (cf. Fig. 147).
Fig. 142. ly after partial postjuv moult, 4 October. MaC and MeC postjuv. GC 1-6+10 juv, 7-9 postjuv, T and rest of wing juv. Recognizable as lyby the conspicuous moult limit within GC. Moult limits within GC 4â&#x20AC;&#x201D;8 are most easily recognizable.
Fig. 143- ly after partial postjuv moult, 20 October. MaC and MeC postjuv. GC 1-5 juv, 6-10 postjuv. T7 juv, 8-9 postjuv. Rest of wing juv. Distinct moult limit within GC. The juv T 7 is only slightly worn, but recognizable as juv by its greyish-brown, not black base which does not contrast with the base of S 6.
Motacilla alba alba
Fig. 144. ly after partial postjuv moult, 4 October. MaC and MeC postjuv. GC 1—3 juv, 4—10 postjuv, T postjuv. Rest of wing juv. Recognizable as ly by the conspicuous moult limit within GC. The postjuv GC have black, the juv GC greyish-brown feather centres. The postjuv T 7 has a black base which contrasts with the juv S 6. Fig. 145. ly after partial postjuv moult, 4 October. MaC and MeC postjuv. GC postjuv. T postjuv. CC postjuv. Al 1 postjuv, 2-3 juv. Rest of wing juv. All GC are similarly fresh and intact and have black feather centres. Such birds are not always easy to distinguish from ad, but can be recognized as ly by the contrast between the postjuv T and juv S, especially between the bases of T 7 and S 6. Futhermore, the renewed CC and Al 1 are slightly darker than the juv PC and Al 2-3.
Fig. 146. ly after partial postjuv moult, 5 October. MaC and MeC postjuv. GC postjuv. T and S 6 postjuv. CC, Al and rest of wing juv. Exceptional ly which renewed S 6 together with all T.
85
Fig. 147. Ad after complete postbr moult, 20 October. Whole wing postbr. Compared with ly with no GC moulted, the contrast between GC and MeC is less distinct (cf. Fig. 139 and 141). Compared with ly with all GC and T moulted, the difference in colour of the bases of T 7 and S 6 is less distinct (cf.Fig. 144 and 145).
Fig. 148. 2y S after partial prebr moult, 11 April. MaC postjuv. MeC 1-3+8 postjuv, 4-7 prebr. GC 1-2 juv, 3—5+10 postjuv, 6—9 prebr. T prebr. Rest of wing juv. Typical 2y with three generations of GC. The juv GC 1-2 are lighter and contrast with the adjacent postjuv GC 3-5 which have darker feather centres. The prebr GC 6—9 show the darkest feather centres and the broadest, most intact fringes. Since the juv GC 1-2 are not exposed on the closed wing, they are not much more worn than the postjuv GC 3—5.
Fig. 149. 2y 9 after partial prebr moult, 15 April. MaC and MeC postjuv. GC 1—2 juv, 3-6+10 postjuv, 7-9 prebr. T 7+9 postjuv, 8 prebr. Rest of wing juv. 2y with three generations of GC. Since this bird is a 9, the colour differences between the three generations of GC are less distinct. Nevertheless, GC 1-2 are recognizable as juv by the browner tinge compared with the adjacent postjuv GC 3-
86
Motacilla alba alba
Fig. 150. 2y after partial prebr moult, 29 April. MaC postjuv. MeC probably all postjuv. GC 1-5 juv, 6-10 prebr. T prebr. Rest of wing juv. In this bird, more GC were moulted during the prebr moult than during the postjuv moult and, hence, only two generations of GC axe present. The juv GC adjoin the prebr GC without being separated by postjuv GC as in Fig. 148 and 149. Such 2y are difficult to distinguish from ad which also show only two generations of GC. They can usually be recognized as 2y by their GC being more bleached than the postbr GC of ad.
Fig. 151. 2y after partial prebr moult, 11 April. MaC postjuv. MeC 1—4+7—8 postjuv, 5-6 prebr. GC 1-6+10 postjuv, 7-9 prebr. CC postjuv. Al 1 postjuv, 2—3 juv. T 7+9 postjuv, 8 prebr. Rest of wing juv. This 2y moulted all GC, CC and Al 1 during an extensive postjuv moult. Thus, there are only two generations of GC present in spring, consisting of postjuv and prebr GC. Such 2y are very difficult to distingush from ad. This bird can be recognized as ly by the postjuv CC and Al 1 contrasting with the juv PC and Al 2—3 in their darker colour.
Fig. 152. Ad after partial prebr moult, 7 May. MaC postbr. MeC 1—2+4—7 prebr, 3+8 postbr. GC 1-6+10 postbr, 7-9 prebr. T 7+9 postbr, 8 prebr. Rest of wing postbr. Recognizable as ad by dark PC edged white (not distinct in all ad), by the broad white fringe of Al 2 and by the dark, only moderately bleached P and S. 2y usually have slightly browner, more bleached P and S (cf. Fig. 149).
Troglodytes troglodytes
87
Troglodytes troglodytes Wren Extent of postjuvenile moult
MaC and MeC: all. GC: range 0-8, mean 4.5, mode 6, no GC 2.8% (N=109). CC: 2.4%. Al: none 84.3%, one 157% (N=83). T: none 60.8%, one 27.5%, two 10.8%, three 1.0% (N=102) (see p. 33). The extent of post] uv moult is correlated among GC, Al and T (Fig. 154). T may be moulted when at least three GC are renewed, Al 1 when at least five GC renewed. The extent of postjuv moult decreases as the autumn migratory season proceeds and is lowest during winter. In spring, birds with a more extensive postjuv moult appear (Fig. 155). This seasonal variation in the extent of postjuv moult is negatively correlated with wing-length (see p. 42 and Jenni & Winkler 1983). In England, ly starting postjuv moult late (probably late-hatched birds) moult no T and fewer GC and R than ly with an early start of postjuv moult (Hawthorn 1971, 1974) Extent of postbreeding moult Whole plumage. Prebreeding moult While Witherby etal. (1943) mentioned no prebr moult, other authors found indications of a limited prebr moult including body-feathers and exceptionally MaC, MeC, shoulder-feathers and underwing-coverts (Vaurie 1951, Glutz & Bauer 1985). Comments on ageing Best criteria: Skull pneumatization until the beginning of December (p. 204). Moult limit within GC and difference in colour between GC and MeC and MaC diagnostic of ly/2y, although sometimes difficult to recognize.
Fig. 153. Extent of postjuv moult on the wing and tail in ly/2y Troglodytes troglodytes.
ly/2y: 97% show a moult limit within GC, which is distinct when among the outer GC (Fig. 159-161), but sometimes difficult to detect when among the inner GC (Fig. 158). Moult limits within GC recognizable by an abrupt change in the individually very variable colour pattern and by differences in length and colour between juv and postjuv GC. Postjuv GC, T and Al have a more bronze tinge, while juv are more reddish-brown. Postjuv GC are often tipped white (Fig. 159 and 161). The CC may, or may not, show a white tip in the juv plumage (cf. Fig. 156 and 157). To recognize ly/2y without any or with few renewed GC, the difference in colour between MaC and MeC, which are always postjuv, and the juv GC is diagnostic. The banding pattern on P 7 and 8 as well as the colour pattern of Al 3 (Drost 1932, Hawthorn 1971) are not a reliable ageing criteria (Jenni & Winkler 1983). Ad: No moult limit within GC. No difference in colour between MaC, MeC and GC. Many, but not all ad show white tips on GC (cf. Fig. 162 and 163).
Fig. 154. Relationships between the number of postjuv GC and the percentage of individuals with renewed Al and T in ly/2y Troglodytes troglodytes which have completed their postjuv moult.
Fig. 155. Mean number of postjuv GC in the course of the year of ly/2y Troglodytes troglodytes which have completed the postjuv moult (the two values for October refer to the first and second half of the month).
Fig. 156. ly in juv plumage, 11 August. Whole wing juv. All GC have the same reddish-brown colour. Note the loosely textured MaC and MeC. CC tipped white.
88
Troglodytes troglodytes
Fig. 157. ly in juv plumage, 14 August. Whole wing juv. MaC and MeC loosely textured, CC without white tip.
Fig. 158. ly after partial postjuv moult, 25 September. MaC and MeC postjuv. GC 1—7 juv, 8-10 postjuv. Rest of wing juv. Moult limit among inner GC not conspicuous. The juv GC are more reddishbrown than the bronze tinged postjuv GC. The bronze tinged postjuv MaC and MeC contrast with the reddish-brown juv GC.
Fig. 161. ly after partial postjuv moult, 18 September. MaC and MeC postjuv. GC 1—3 juv, 4—10 postjuv. CC postjuv. Al 1 postjuv, 2—3 juv. T 7—8 juv, 9 postjuv. Rest of wing juv. Moult limit within GC best recognized by the difference in colour between juv and postjuv GC. Postjuv GC 4-6 tipped white.
Fig. 159. ly after partial postjuv moult, 14 October. MaC and MeC postjuv. GC 1—4 juv, 5—10 postjuv. Rest of wing juv. Juv GC reddish-brown, less spotted, and without white tips. Postjuv GC with prominent dark spots, tinged bronze and with white tips on GC 5-7. Fig. 162. Ad after complete postbr moult, 3 October. Whole wing postbr. No moult limit within GC. All GC have a similar colour pattern without abrupt change. Almost no difference in colour between MaC, MeC and GC. This bird has no white tips on GC.
Fig. 163. Ad after complete postbr moult, 29 October. Whole wing postbr. No moult limit within GC which all have a similar colour pattern. In this bird, the outer GC are tipped white.
Fig. 160. ly after partial postjuv moult, 18 September. MaC and MeC postjuv. GC 1—5 juv, 6—10 postjuv. Al 1 postjuv, 2—3 juv. T 7—8 juv, 9 postjuv. Rest of wing juv. Recognizable as ly by moult limits within GC and T. Postjuv GC and T tinged bronze and with distinct dark marks, resulting in an abrupt change of the colour pattern within the row of GC, No white tips on postjuv GC.
Prunella modularis
89
Prunella modularis Dunnock Extent of postjuvenile moult MaC and MeC: usually all. MeC may remain partially unmoulted. GC: range 0-10, mean 1.4, mode 0, no GC 60.0%, all GC 0.7% (N=1806). CC: 3.4%. Al: none 89.7%, one 9.5%, two 0.8% (N=1357). T: none 96.9%, one 2.2%, two 0.6%, three 0.3% (N=1355) (see p. 33). R: we could detect regular moult of R, as cited in the literature (e.g. Cramp 1988), in only one bird (Fig. 173) which had all GC, CC,, Al 1, all T and all R renewed. The extent of postjuv moult is correlated among GC, CC, Al and T (Fig. 165). The extent of postjuv moult decreases as the autumn migratory season proceeds (Fig. 166). In NW Russia, the postjuv moult is slightly less extensive than in Switzerland (Rymkevich 1990): all ly moult the MeC, 30% at least one GC (usually up to three, occasionally up to seven), 4% renew Al, 2% CC and one bird T. Extent of postbreeding moult Whole plumage. Comments on ageing Best criteria: Skull pneumatization until at least the beginning of November (p. 204). At least until the end of October, the colour of the iris is diagnostic in most birds. Usually, ad have a reddish-brown and ly a greyish-brown or greyish-olive iris, while birds with an intermediate iris colour may be ad or ly. Among 788 ly and 160 ad studied between July and October, 10% of ly and 9% of adults had an intermediate colour and only 0.4% of ly had already acquired the adulttype iris colour. There was no apparent seasonal trend. According to Spencer & Mead (1978a), the iris colour can be used up to at least
Fig. 165. Relationships between the number of postjuv GC and the percentage of individuals with renewed CC, Al and T in lyI'2y Prunella modularis which have completed their postjuv moult.
Fig, 166. Percentage of ly Prunella modularis with at least one postjuv GC during autumn (data grouped in fiveday periods; the first value includes the period 9-28 August, the last 23 October-6 November).
Fig. 164. Extent of postjuv moult on the wing and tail in ly/2y Prunella modularis. December. Ageing based exclusively on plumage characters is often difficult and should only be done with experience acquired by using other characters in addition. ly/2y: A few birds retain juv MeC, recognizable by the yellow, not rusty-brown tips (Fig. 168). 39% of ly/2y show a moult limit within GC which is usually recognizable by differences in colour and shape of the light tips between juv and postjuv GC. However, due to individual variability in these tips, moult limits are difficult to detect in some birds. Conspicuous moult limits as in Fig. 173 are rare. On juv GC, tips are yellowish, conspicuous on GC 2â&#x20AC;&#x201D;9, and present on both webs of the inner juv GC; the black field around the shaft is well-defined, especially in the terminal part which contrasts well with the light tips. Postjuv GC (typical in Fig. 174) have ill-defined whitish tips which fade into the terminal black field and may be virtually absent on the innermost GC (GC 9 in Fig. 169, GC9-10 in Fig. 170). Outer renewed GC often have a greyish tinge (Fig. 172 and 175). Most ly/2y have no moult limit within GC. Those with well-defined tips on outer and inner webs of GC 8 and 9 can be aged ly/2y up to spring. Ad: Unless skull pneumatization and iris colour can be used, identification of ad is difficult in some cases. Usually, ad have whitish tips on the outer GC and inconspicuous or missing tips on the inner GC. Light tips, black field around the shaft and brownish fringes are ill-defined and fade into each other.
Fig. 167. ly at the beginning of partial postjuv moult, 9 August. Whole wing juv, except some growing MaC. MeC and inner GC with yellowish tips on outer and inner web.
90
Prunella modularts Fig. 168. \j after partial postjuv moult, 13 October. MaC postjuv, MeC 1-5 juv, 6-8 postjuv. GC and rest of wing juv. Juv MeC tipped yellowish. Tips on inner GC yellowish and well-defined.
Fig. 169. ly after partial postjuv moult, 24 September. MaC and MeC postjuv. GC 1â&#x20AC;&#x201D;8+10 juv, 9 postjuv. Rest of wing juv. Renewed GC 9 without distinct light tips, black field around the shaft less conspicuous than on the adjacent GC.
Fig. 173. ly after partial postjuv moult, 29 September. Exceptionally, this bird has seven S (but three T) and 11 GC. MaC and MeC postjuv. GC 1-3 juv, 4-11 postjuv. CC postjuv, Al 1 juv or postjuv, 2-3 juv. Innermost T postjuv. Rest of wing juv. Exceptionally conspicuous moult limit within GC. GC 1â&#x20AC;&#x201D;3 with yellowish, well-defined tips, renewed GC with whitish and ill-defined tips.
Fig. 170. 2y after partial postjuv moult, 17 April. MaC and MeC postjuv. GC 1-8 juv, 9-10 postjuv. Rest of wing juv. Renewed GC 9 and 10 virtually without light tips, less worn and more firmly textured than juv GC.
Fig. 171. ly after partial postjuv moult, 9 Sept. MaC and MeC postjuv. GC 1-4, 6-7+10 juv, 5+8-9 postjuv. Rest of wing juv. GC 5 with only a faint and ill-defined light tip. GC 8 and 9 without light tips. All juv GC have a more conspicuous black area around the shaft than the postjuv GC.
Fig. 174. ly after partial postjuv moult, 3 October. MaC and MeC postjuv. GC postjuv. CC and Al 1 postjuv, 2-3 juv. T 7-9 postjuv. PC 1-3+5 postjuv. Rest of wing juv. Exceptional case of a very extensive postjuv moult. Recognizable as ly by the moult limit between postjuv T 7 and juv S 6.
Fig. 172. Ad after complete postbr moult, 13 April. Whole wing postbr. Tips already worn, whitish and ill-defined.
Fig. 175. Ad after complete postbr moult, 29 September. Whole wing postbr. Inner GC with ill-defined light tips, fading into the black field around the shaft. Outer GC tipped whitish.
Erithacus rubecula
91
Erithacus rubecula Robin Extent of postjuvenile moult MaC and MeC: usually all. Exceptionally, individual juv MaC and MeC may be retained by ly moulting no or few GC. GC: range 0-10, mean 4.7, mode 5, no GC 0.03%, all GC 0.05%
(N=ll,108). CC: 11.7%. Al: none 75.0%, one 24,9%, two 0.1% (N=8701). T: none 99.8%, one 0.2% (N=8499). R: none 99.9%, one (R 1) 0.1% (N=8490). The extent of postjuv moult is correlated among GC, CC and Al (Fig. 177). CC and Al may be renewed when at least three GC are moulted. The extent of postjuv moult decreases as the autumn migratory season proceeds. It is lowest in early winter and increases again during late winter and spring (Fig. 178). During April, there is no trend in the number of GC moulted. Spring migrants (March, April) on Ventotene Island, Italy (not included in Fig. 178) have slightly more GC moulted than spring birds in Switzerland (Italy: mean 4.5, N=492; Switzerland: mean 4.3, N=1252, difference not significant). In NW Russia, the postjuv moult includes all MaC and MeC, one to six GC, none to three Al, never CC, and T 9 in one bird only. The extent of postjuv moult was found to depend on hatching date: while early-hatched Russian birds renew usually five to six GC and Al, latehatched birds moult only two to three GC and no Al (Rymkevich 1990). In ly birds caught in Sweden at Falsterbo and Ottenby, the postjuv moult is slightly less extensive than in birds caught in Switzerland (mean 4.4â&#x20AC;&#x201D;4.5 renewed GC, re-calculated on the basis of ten GC; Karlsson et al. 1986a, Pettersson etai 1990). At Falsterbo, no bird was found having all or fewer than three GC moulted. At both sites, the number of GC moulted decreases during autumn migration (at Falsterbo from about 4.6 at the beginning of September to about 3.5 at the end of October). During spring migration at Falsterbo no seasonal trend is observed (Karlsson etaL 1986a). Based on a small data
Fig. 177. Relationships between the number of postjuv GC and the percentage of individuals with renewed CC and Al in ly/2y Erithacus rubecula which have completed their postjuv moult.
Fig. 176. Extent of postjuv moult on the wing and tail in ly/2y Erithacus rubecula.
set, Pettersson et al. (1990) concluded that birds wintering in the E Mediterranean (Greece and Cyprus) have fewer postjuv GC than birds wintering in the W Mediterranean (S France and Spain). There is probably no difference in the extent of postjuv moult between the sexes (Karlsson etal. 1986a). Extent of postbreeding moult Whole plumage. Suspension of primary moult in one bird after renewal of P 1-3 was due to remating and a second breeding attempt (Harper 1984). One ad retained PC 5 (Fig. 191). Comments on ageing Best criteria: Moult limit within GC diagnostic in almost all ly/2y. Skull pneumatization until mid-September, but many ly have incomplete pneumatization until the beginning of November (p. 204). Supplementary ageing criteria which leave some birds undetermined are given below. ly/2y: 99.9% show a moult limit within GC which is usually easily recognized. Juv GC can always be distinguished from postjuv GC by differences in the colour of the feather centre and outer fringe, irrespective of the distinctness of the light tips. Juv GC are brown with a yellow-brownish tinged fringe, postjuv GC have an olive tinge on the fringe and feather centre. The light tips of GC vary individually, but, when present, may be used to detect the moult limit. In many ly/2y birds, light tips are present on juv GC, but not on postjuv GC (Fig. 182). Birds having light tips on all GC show an abrupt change in shape and colour of the light tips at the moult limit (Fig. 183), This sudden change is not present in ad showing light tips on GC (Fig. 189 and 190). ly/2y with small (Fig. 185), worn off (Fig. 184) or missing (Fig. 186) light tips on GC are recognizable by differences in the colour of the feather centres between juv and postjuv GC. The very few ly/2y with all GC moulted (0.05%) show a contrast between the olive tinged CC and Al 1, which are always renewed in these birds, and the browner juv Al 2-3 and PC (Fig. 187). Ad: No moult limit within GC and no contrast between CC, Al and PC. Fringes of PC tinged olive, similar to GC. The light tips on GC are generally smaller and often absent (Fig. 188). Ad with light tips on GC show a gradual decrease in size from outside to inside and gradual change in shape (Fig. 189 and 190).
Fig. 178. Mean number of postjuv GC in the course of the year ofly/2y Erithacus rubecula which have completed the postjuv moult (from August until October: five-day periods; the first value includes the period 30 July-18 August).
Other criteria: A number of other ageing criteria have been described and tested on a large number of birds (Pettersson 1983, Karlsson et al. 1986a, Pettersson et al. 1990). They may be useful to some ringers as
92
Erithacus rubecula
supporting criteria, but leave some birds undetermined or assigned to the wrong age class. Usually, ly have a yellowish inside to the upper mandible in autumn and still some yellow left in spring, but in autumn and especially in spring, this feature may be unclear or misleading (Frelin 1971, Pettersson 1983, Karlsson et ai 1986a, Svensson 1992, own obs.). In ly/2y, the R and PC are usually, but not always (cf. Fig. 187), more pointed and the colour of the iris and the legs darker than in ad (Karlsson et aL 1986a, Pettersson etal. 1990).
Fig. 179. ly in juv plumage, 11 August. Whole wing juv. MaC, MeC and all GC tipped yellowish, typical of the juv plumage.
Fig. 180. 2y after partial postjuv moult, 23 April. MaC mostly postjuv, a few at the edge of the wing juv. MeC 1-3 juv, 4—8 postjuv. GC and rest of wing juv. Very rare case of a 2y without any GC moulted. Recognizable as 2y by the retained juv MaC and MeC.
Fig. 181. ly after partial postjuv moult, 14 October. MaC and MeC postjuv. GC 1—8+10 juv, 9 postjuv. Rest of wing juv. Recognizable as ly by the renewed GC 9 tinged olive and without light tip.
Fig. 182. ly after partial postjuv moult, 20 September. MaC and MeC postjuv. GC 1—5 juv, 6—10 postjuv. Rest of wing juv. Conspicuous and typical moult limit within GC. Postjuv GC tinged olive and without light tips, juv GC browner and with large tips.
Fig. 183. ly after partial postjuv moult, 14 September. MaC and MeC postjuv. GC 1—4 juv, 5—10 postjuv. CC postjuv. Al 1 postjuv, 2—3 juv. Rest of wing juv. Moult limit within GC recognizable by the difference in colour of the feather centres and by the abrupt change in size, shape and colour of the light tips. The renewed CC and Al 1 are tinged olive, but not the juv Al 2-3 and PC. Fig. 184. 2y after partial postjuv moult, 10 April. MaC and MeC postjuv. GC 1-2 juv, 3-10 postjuv. CC postjuv. Al 1 postjuv, 2—3 juv. Rest of wing juv. Although the GC are heavily worn, the moult limit within the GC is still easily recognized by the difference between the browner juv GC 1-2 and the greenish-grey postjuv GC 3—10. The postjuv CC and Al 1 contrast with the juv Al 2—3 and PC in their greenish-grey colour.
Fig. 185. ly after partial postjuv moult, 14 September. MaC and MeC postjuv. GC 1—6 postjuv, 7—10 juv, Al 1 postjuv, 2-3 juv. Rest of wing juv. Moult limit within GC recognizable by the difference in colour between the browner juv GC and the olive tinged postjuv GC, but hardly recognizable by the pattern of tips. Juv GC only faintly tipped.
Erithacus mbecula
93
Fig. 186. 2y after partial postjuv moult, 19 April. MaC and MeC postjuv. GC 1-7 juv, 8-10 postjuv. Rest of wing juv. Juv GC without light tips, recognizable by their browner colour and more worn fringes, postjuv GC by their olive tinge.
Fig. 189. Ad after complete postbr moult, 13 April. Whole wing postbr. As Fig. 188, but with small tips on GC. The tips decrease gradually in size from outside to inside without abrupt change.
Fig. 187. ly after partial postjuv moult, 22 September. MaC and MeC postjuv. GC all postjuv. CC postjuv. Al 1 postjuv, 2-3 juv. Rest of wing juv. Rare case of a ly with all GC moulted on the right wing (left wing: GC 1-2 juv). Recognizable as ly by the renewed Al 1 and CC which contrast with the juv Al 2â&#x20AC;&#x201D;3 and PC in their olive tinge. GC more olive than the juv PC and S.
Fig. 190. Ad after complete postbr moult, 17 September. Whole wing postbr. Exceptional ad with very large tips on GC. Recognizable as ad by the gradual, not abrupt, change in size and shape of the light tips over the GC and by the similarly coloured fringes of GC and PC.
Fig. 191. Ad after complete postbr moult, 21 September. Whole wing postbr except PC 5. Typical ad with only faint tips on GC. All GC of the same colour. Exceptionally, PC 5 has been retained.
Fig. 188. Ad after complete postbr moult, 27 September. Whole wing postbr. No moult limit within GC and Al and between CC and PC. All GC uniformly tinged olive. Typical ad without light tips on GC.
94
Luscinia megarhynchos
Luscinia megarhynchos Nightingale Extent of postjuvenile moult MaC and MeC: all. GC: range 3-9, mean 5.3, mode 5 (N=120). CC: 3.9%. Al: none 97.1%, one 2.9% (when at least seven GC renewed) (N= 102). T: none 98.0%, one 2.0% (N=102).
Extent of postbreeding moult Whole plumage.
Fig. 192. Extent of postjuv moult on the wing and tail in ly/2y Luscinia megarhynchos.
Comments on ageing Best criteria: Skull pneumatization until at least the beginning of October (p. 204). Moult limit within GC diagnostic of ly/2y. ly/2y: Moult limits within GC are usually easily recognizable by the presence of buffish tips on juv GC (Fig. 195). Occasionally, these tips are not distinct (Fig. 193). Therefore, it is advisable to always check for differences in colour of the feather centres between juv and postjuv GC. Juv GC are slightly more rusty-brown, of looser texture and often shorter than postjuv GC. Moreover, PC of ly/2y are narrower and more pointed than in ad and often have inconspicuous pale tips. In spring, the plumage is often surprisingly little abraded, so that the pale tips on juv GC are still visible (Fig. 194 and 195). Ad: All GC of similar colour and texture and without pale tips (Fig. 196 and 197). Fig. 195. 2y after partial postjuv moult, 18 April. MaC and MeC postjuv. GC 1-6 juv, 7-10 postjuv. Rest of wing juv. Conspicuous moult limit within GC recognizable by the presence of distinct pale tips on juv GC. Although a spring bird, the plumage is hardly worn. Fig. 193. ly after partial postjuv moult, 25 August. MaC and MeC postjuv. GC 1â&#x20AC;&#x201D;5 juv, 6-10 postjuv. Rest of wing juv. Juv GC without or with only small illdefined pale tips. Moult limit recognizable mainly by a slight difference in colour of the feather centres between juv and postjuv GC.
Fig. 194. 2y after partial postjuv moult, 4 May. MaC and MeC postjuv. GC 1-3 juv, 4-10 postjuv. Rest of wing juv. Juv GC with pale tips, slightly more rusty feather centres and looser textured than postjuv GC.
Fig. 196. Ad after complete postbr moult, 12 August. Whole wing postbr. GC without pale tips and of similar colour, texture and length. PC broader and more rounded than in ly/2y.
Fig. 197. Ad after complete postbr moult, 20 April. Whole wing postbr. GC all similar in colour, texture and length and without pale tips. Although a spring bird, all feathers are surprisingly fresh.
Luscinia svecica
95
Luscinia svecica Bluethroat Extent of postjuvenile moult
MaC and MeC: all. GC: range 1-8, mean 2.9, mode 2 (N=74). CC: 12.8%. Al: none 94.9%, one 5.1% (N=39). TandR: one bird had T 7, another T 7-9 and R 1-5 renewed (N=64). In NW Russia, the postjuv moult includes all MeC, usually one to three GC (depending on the site 10—30% retain all juv GC) and occasionally CC and one or two Al (Rymkevich 1990). Fig. 198. Extent of postjuv moult on the wing and tail in ly/2y Luscinia svecica.
Extent of postbreeding moult Whole plumage.
autumn migration scores 3-5 occur (N=46). Light tips on juv GC and moult limit within GC diagnostic of ly/2y.
Extent of prebreeding moult The prebr moult comprises only the feathers of chin, throat and sides of head or may be completely suppressed (Glutz & Bauer 1988, Roselaar in Cramp 1988). Comments on ageing Best criteria: Skull pneumatization until at least October. During
ly/2y: Juv GC with rusty-buff tips, which are often still present in spring, but may be abraded from about May onwards. Postjuv GC with more greyish feather centres than juv GC. Many ly/2y show more or less distinct light tips on CC, Al and PC. Ad: GC without rusty-buff tips, but only narrow and slightly lighter fringes. Exceptionally, ad may show light tips on GC (Svensson 1992). Thus, always check for uniformity of colour of feather centres.
Fig. 201. Ad after complete postbr moult, 19 September. Whole wing postbr. No light tips on GC. All GC show similarly coloured feather centres. Fig, 199, ly after partial postjuv moult, 12 September. MaC and MeC postjuv. GC 1—8 juv, 9—10 postjuv. Rest of wing juv. Distinct moult limit within GC. Juv GC with rusty tips, postjuv GC without tips and with more greyish feather centres. Fig. 200. ly after partial postjuv moult, 16 August. MaC and MeC postjuv. GC 1—5 juv, 6-10 postjuv. Rest of wing juv. Moult limit within GC recognizable by the presence of light tips on juv GC, but also by a difference in colour of the feather centres between juv and postjuv GC.
Fig. 202. Ad after complete postbr moult, 15 April. Whole wing postbr. No light tips on GC and uniformly coloured feather centres.
96
Phoenicurus ochruros
Phoenicurus ochruros Black Redstart Extent of postjuvenile moult MaC and MeC: all. GC: range 0-10, mean 3.5, mode 2, no GC 1.0%, all GC 0.2% (N=477). CC: 4.3%. Al: none 85.9%, one 14.1% (N=398). T: none 87.6%, one 5.7%, two 5-0%, three 1.7% (N=418) (see p. 33). R: none 99.2%, one 0.8% (N=394). S: two birds moulted S 6 on one wing.
The extent of postjuv moult is correlated among GC, CC, Al and T (Fig. 204). The extent of postjuv moult decreases slightly but significantly as the autumn migratory season proceeds (Fig. 205). Extent of postbreeding moult Whole plumage. Prebreeding moult The indication of a possible prebr moult found in some publications probably goes back to a footnote in Witherby et al. (1943) mentioning two birds with growing body-feathers in February and March, but qualifying them as 'abnormal'. Among 108 birds (ad and 2y) examined by us in Italy and Switzerland during March and April, three had a few growing body-feathers and none showed feathers renewed during winter or spring. Thus, there is no, or only a very restricted, prebr moult in this species. Comments on ageing Best criteria: Skull pneumatization until the end of August (p. 204). Most ly/2y recognizable by moult limits within GC and T. ly/2y: 98.8% show a moult limit within GC. In ly $ in the ad-d1 -like plumage (^paradoxus morph), moult limits are conspicuous; juv GC
Fig. 203. Extent of postjuv moult on the wing and tail in ly/2y Phoenicurus ochruros.
are brown with narrow bufFish fringes, postjuv GC are dark grey with broad grey fringes (Fig. 208, 209 and 212). In 6 in the 9 -like plumage ('cairet morph) and in ?, moult limits are more difficult to recognize, especially when within the inner GC (Fig. 207 and 210). The postjuv GC have darker feather centres tinged greyish and darker fringes than the juv GC. Moult limits within outer GC are more distinct (Fig. 211-213). Some ly/2y with more than four GC moulted and all ly/2y with more than eight GC moulted show a moult limit within T or between T and the browner juv S (Fig. 212 and 214). Moult limits are still easily recognized in spring, but are obscured by wear in summer. A supporting, though not infallible, criterion is the pattern of the outermost R. Juv R 6 generally has dark marks on the tip and a dark shaft extending more than 9 mm from the tip inwards; R 6 of ad shows less prominent dark markings extending less than 8 mm from the tip inwards or (more rarely) is completely red (Svensson 1992). Ad: cT are recognizable by their uniformly greyish-black wing and by having white outer fringes not only on T but also on inner S (Fig. 215 and 216). 9 are recognizable by the lack of a moult limit within GC and T, by darker fringes on GC resulting in less contrast between feather centre and fringe than in ly/2y and by a similar colour of T and S.
Fig. 204. Relationships between the number of postjuv GC and the percentage of individuals with renewed CC, Al and T in ly/2y Phoenicurus ochruros which have completed their postjuv moult.
Fig. 205. Mean number of postjuv GC during autumn (data grouped in ten-day periods; the first value includes the entire August) and in spring of ly/2y Phoenicurus ochruros which have completed the postjuv moult.
Fig. 206. ly S at the beginning of partial postjuv moult, 5 August. MaC partly postjuv. Rest of wing juv. Recognizable as S by the renewed MaC having black feather centres and grey fringes. Exceptionally, juv T 7 shows some white at the base of the outer web.
Phoenicurus ochruros
97
Fig. 207. ly after partial postjuv moult, 15 October. MaC and MeC postjuv. GC 1-8 juv, 9-10 postjuv. Rest ofwingjuv. Inconspicuous moult limit within GC of a 9 or a 3 in 9 -like plumage. The renewed GC are slightly darker with a greyish tinge and less worn than the juv GC.
Fig. 208. ly 6 after partial postjuv moult, 16 October. MaC and MeC postjuv. GC 1-7 juv, 8-10 postjuv. Rest ofwingjuv. Conspicuous moult limit within GC, typical of 6. The postjuv GC are grey, the juv GC brown.
Fig. 209. 2y 3 after partial postjuv moult, 6 April. MaC and MeC postjuv. GC 1—8 juv, 9-10 postjuv. Rest of wing juv. Conspicuous moult limit within GC, typical of 6.
Fig. 212. ly c5 after partial postjuv moult, 2 October. MaC and MeC postjuv. GC 1—3 juv, 4—10 postjuv. Al 1 postjuv, 2—3 juv. T 7—9 postjuv. Rest of wing juv. Distinct moult limit within GC. The postjuv T contrast with the juv S and have white outer fringes, typical of ly <? in partial ad <3 plumage.
Fig. 213. ly after partial postjuv moult, 18 October. MaC and MeC postjuv. GC 1—3 juv, 4—10 postjuv. T 7 juv, 8-9 postjuv. Rest of wing juv. Inconspicuous moult limit within GC of a 9 or a cT in 9 -like plumage. The postjuv GC have darker feather centres with a slight greyish tinge and darker fringes than the juv GC.
Fig. 210. 2y after partial postjuv moult, 20 April. MaC and MeC postjuv. GC 1-8 juv, 9-10 postjuv. Rest of wing juv. Inconspicuous moult limit within GC. The renewed GC are darker, with a greyish tinge and less worn than the juv GC.
Fig. 211. 2y after partial postjuv moult, 16 April. MaC and MeC postjuv. GC 1-4 juv, 5-10 postjuv, T 7 juv, 8—9 postjuv. Rest of wing juv. The juv GC are more bleached and have a lighter, more conspicuous fringe than the postjuv GC.
Fig. 214. 2y after partial postjuv moult, 11 April. MaC and MeC postjuv. GC 1 juv, 2-10 postjuv. CCand Al 1 postjuv. T 7 juv, 8-9 postjuv. Rest of wing juv. Recognizable as 2y by the juv GC 1 with its light fringe and brown feather centre and by the moult limit within T.
98
Phoenicurus ochruros Fig. 217. Ad 9 after complete postbr moult, 16 October. Whole wing postbr. No moult limit within GC, T and between T and S. Fringes of GC slightly darker than in ly (cf. Fig. 207).
Fig. 215-Ad 6 after complete postbr moult, 18 October. Whole wing postbr. Whole wing greyish-black without moult limit. Outer webs of T and inner S white.
Fig. 216. A d d after complete postbr moult, 9 April. Whole wing postbr. Easily recognizable as ad <S by the white fringes on the T and inner S. Whole wing grey-black without moult limit.
Fig. 218. Ad 9 after complete postbr moult, 16 April. Whole wing postbr. No moult limit within GC and T. The fringes of the GC contrast less with the feather centres than in ly/2y.
Phoenicurus phoenicurus
99
Phoenicurus phoenicurus Redstart Extent of postjuvenile moult
MaC and MeC: all. GC: range 0-6, mean 2.1, mode 2, no GC 1,8% (N=891). CC: 0.2%. Al: none 98.8%, one 1.2% (N=581). 8 moult slightly but significantly more GC than 9: 8.8% of cT and 14.6% of 9 moult none or one GC, 68.4% of 3 and 69.0% of 9 moult two GC and 22.8% of <J and 16.4% of 9 moult more than two GC. There is no significant trend of the extent of GC-moult with season (Fig. 220). In NW Russia, CC and Al are not moulted, but, similar to Switzerland, on average 2.2 GC (Rymkevich 1990).
Fig. 219. Extent of postjuv moult on the wing and tail in ly/2y Phoenicurus phoenicurus.
Extent of postbreeding moult Whole plumage. Comments on ageing Best criteria: Moult limit within GC usually diagnostic in cJ, but difficult to recognize in 9. Skull pneumatization until mid-August (p. 204). ly/2y: 98% show a moult limit within the inner GC, which is conspicuous in c?, but difficult to recognize in 9. Thus, 9 should be aged only by experienced observers. In <3, juv GC have buffish-brown outer fringes, and postjuv GC greyish outer fringes but brownish tips (Fig. 221â&#x20AC;&#x201D;222). In 9, juv and postjuv GC can be recognized mainly by differences in wear, but also in colour: postjuv GC are less worn and have slightly darker feather centres and fringes than juv GC. In some 9, moult limits are more conspicuous than in others (cf Fig. 224 and 225). In spring, the same criteria can be applied, but ageing 9 is even more difficult, although differences in wear may be more pronounced (Fig. 226). In cj, the grey fringes of postjuv GC may be worn off and recognizable only at the base of the feather (Fig. 223). The few ly/2y with no GC moulted have a yellowish tip on the juv GC 10 which is absent on the renewed GC 10. Ad: No moult limit within GC. GC 10 without light tip. In cJ, all GC and CC have grey outer fringes (Fig. 227 and 228). On average, ad cJ are more brightly coloured than ly/2y cJ, i.e. the black on the throat, the orange on the breast and the white band on the forehead are less concealed by light feather tips, but this is far from an infallible criterion (Fig. 42).
Fig. 220. Mean number of postjuv GC during autumn of <5 (dots) and 9 (triangles) ly Phoenicurus phoenicurus which have completed the postjuv moult (data grouped in five-day periods; the first value includes the period 30 July-13 August, the last 8-22 October).
Fig. 221. ly 6 after partial postjuv moult, 18 August. MaC and MeC postjuv.
GC 1-6 juv, 7-10 postjuv, Rest of wing juv. Conspicuous moult limit within GC. The postjuv GC are recognizable by their grey outer fringes (but brown tips) and darker feather centres tinged grey. Fig. 222. ly 6 after partial postjuv moult, 9 August. MaC and MeC postjuv. GC 1â&#x20AC;&#x201D;7 juv, 8-10postjuv.Al 1 postjuv, 2-3 juv. Rest of wing juv. Recognizable as ly by the conspicuous moult limit within GC as well as by the postjuv Al 1.
Fig. 223. 2y $ after partial postjuv moult, 14 April. MaC and MeC postjuv. GC 1-7 juv, 8-10 postjuv. Rest of wingjuv. Although heavily worn, the moult limit within GC is still conspicuous.
100
Phoenicurus phoenicurus Fig. 224. ly 9 after partial postjuv moult, 14 August. MaC and MeC postjuv. GC 1-7 juv, 8-10 postjuv. Rest of wing juv. In this 9, the moult limit within GC is comparatively distinct. The postjuv GC are recognizable by darker feather centres tinged greyish as well as greyish-brown and less buffish outer fringes.
Fig. 228. Ad cT after complete postbr moult, 9 May. Whole wing postbr. Although considerably worn, the grey fringes at the bases of the outer GC and CC are still visible and diagnostic of ad.
Fig. 225. ly 9 after partial postjuv moult, 2 September. MaC and MeC postjuv. GC 1-8 juv, 9-10 postjuv. Rest of wing juv. The moult limit within GC in this 9 is difficult to recognize. The postjuv GC are slightly darker and less worn than the juv GC.
Fig. 229. Ad 9 after complete postbr moult, 24 September. Whole wing postbr. Recognizable as ad in having all GC similarly coloured and less buffish fringes than juv GC.
Fig. 226. 2y 9 after partial postjuv moult, 6 May. MaC and MeC postjuv. GC 1-8 juv, 9-10 postjuv. Rest of wing juv. In this 9, the moult limit is comparatively distinct and recognizable by differences in wear and in the colour of the feather centres.
Fig. 230. Ad 9 after complete postbr moult, 24 April. Whole wing postbr. Feather centres of all GC similarly coloured. Their fringes are slightly greyer than in 2y(cÂŁFig.226).
Fig. 227. Ad 6 after complete postbr moult, 11 September. Whole wing postbr. All GC and CC have grey outer fringes, at least near the base.
Saxicola rubetra
101
Saxicola rubetra Whinchat Extent of postjuvenile moult MaC: about 75% moult all, 25% retain some juv MaC. MeC: about one third moult all, two thirds retain one to rarely all juv MeC. GC: range 0-7, mean 1.4, mode 2, no GC 24.1% (N=199). Up to the end of August, the percentage of ly having at least one GC moulted is significantly higher (91%, N=75) than thereafter (66.4%, N=122). In NW Russia, none to four GC are moulted, usually GC9-10 (59.5% of ly, N=179); one bird moulted the CC (Rymkevich 1990). Extent of postbreeding moult Whole plumage. Comments on ageing after the postjuvenile and postbreeding moult Best criteria: The colour of the inside of the upper mandible is diagnostic throughout autumn. In ly, it is pink-grey or yellowish, in ad black or slate-grey. Moult limits within GC and MeC usually diagnostic of ly. Since the skull pneumatizes very rapidly (p. 204), skull pneumatization cannot be used to age fully pneumatized birds in autumn. ly: 76% show a moult limit within GC, usually within the innermost GC. Postjuv GC can be distinguished from juv GC mainly by being less worn and slightly darker (Fig. 236 and 237) or by being mostly white (Fig. 238). Most juv GC 9 and 10 have a buffish shaft-streak, which can however be missing (Fig. 235) or occasionally be present on postjuv GC of 5 . Those ly with no GC moulted can be recognized by moult limits within MeC (Fig. 235). Inner juv MeC always have a buffish shaft-streak, outer juv MeC may have one (Fig. 233) or not (Fig. 234). Ad: GC hardly worn and, like the PC, with darker feather centres than in ly. No moult limits within GC and MeC. Extent of prebreeding moult: 2y and ad MaC: 92% renew all or almost all MaC, 7% part and 1% none (N=231).
Fig. 232. Extent of prebr moult on the wing and tail in ad and 2y Saxicola rubetra. For differences between ad and 2y see text.
Fig. 231. Extent of postjuv moult on the wing and tail in ly Saxicola rubetra.
MeC: 22.5% moult all, 74.5% one to seven and 3% (no GC moulted) none (N=231). 2y birds moult significantly more MeC (mean 5.9, N=143) than ad (mean 4.8, N=60). GC: range 0-7, mean 3.2, mode 3, no GC 11.3% (N=257). 2y birds moult significantly more GC (mean 3.6, N=142) than ad (mean 2.2, N=54). T; none 91.4%, one 8.6% (mostly T 9, partly on one wing only), one bird renewed T 7-9 on the left and T 8-9 on the right wing (N=257). 10.6% of 2y (N=142), but only 3.7% of ad (N=54) renewed at least oneT. R: Regular moult of R was recorded in two birds only (R 1 and R 1â&#x20AC;&#x201D;2, N=257). Rymkevich (1990) recorded a prebr moult of similar extent in NW Russia: most or all feathers on head, underparts and shoulders were renewed. 60% of the individuals renewed all MaC, 32% part and 7% none. 27% moulted all MeC, 46% most, 22% half and 5% none. GC: 0-10, mean 3.9, mode 4, no GC 9.3%, all GC 3.6% (N=54). 7% renewed Al and some the CC. One bird renewed T 9 on one wing only and one bird R 2-6. Comments on ageing after prebreeding moult Ageing spring birds is difficult and needs some experience. Moult limits due to the prebr moult occur in 2y and ad. Usually, the juv GC of 2y are more worn and slightly more bleached than the postbr GC of ad (cf. Fig. 241 and 242 as well as 243 and 244). These differences are more pronounced in <J than in 2. Only three birds out of 257 had three feather generations within GC (Fig. 245). The extent of white on the inner GC and MeC varies strongly between individuals and cannot be used to age spring birds reliably, but is helpful in sexing (Svensson 1992). The extent of white on PC and the outer vanes of P 3-5 also varies between individuals and is of limited use for ageing in spring as well as in autumn.
102
Saxicola rubetra Fig.237.ly 9 after partial postjuv moult, 23 August. MaC and MeC postjuv. GC 1—8 juv, 9-10 postjuv. Rest of wing juv. All MeC fresh, of the same length and of firm texture. The renewed GC 9-10 are slightly darker and less worn than the juv GC and have no buffish shaftstreaks.
Fig. 233. ly in juv plumage, 3 August. Whole wing juv. All MaC, MeC and GC 9-10 with huffish shaft-streaks, typical of the juv plumage.
Fig. 234. ly in juv plumage, 3 August. Whole wing juv. Although in juv plumage, this bird lacks the huffish shaftstreaks on MeC 1—4.
Fig. 235. ly after partial postjuv moult, 13 August. MaC postjuv. MeC 1-4 juv, 5-8 postjuv. GC and rest of wing juv. Recognizable as ly by the moult limit within MeC. Note that this bird lacks the huffish shaft-streaks on the juv GC 9 and 10, usually typical of the juv plumage.
Fig. 236. ly 9 after partial postjuv moult, 27 September. MaC postjuv. MeC 1—4 juv, 5-8 postjuv. GC 1-9 juv, 10 postjuv. Rest of wing juv. The postjuv MeC 5-8 are shorter and of firmer texture than the juv MeC. The postjuv GC 10 has no buffish shaft-streak, is slightly darker and less worn than the juv GC.
Fig. 238. ly cT after partial postjuv moult, 16 September. MaC and MeC postjuv. GC 1—8 juv, 9—10 postjuv. Rest of wing juv. The postjuv GC 9-10 have the typical white colour of &. They contrast with the adjacent juv GC in being less worn.
Fig. 239. Ad (5 after complete postbr moult, 29 September. Whole wing postbr. Whole wing fresh and without moult limits. GC and PC slightly darker than in ly.
Saxicola rubetra
103
Fig. 243. 2y 9 after partial prebr moult, 2 May. MaC mostly prebr. MeC 1-5+8 prebr, 6—7 postjuv. GC 1-7 juv, 8-10 prebr. Rest of wing juv. The GC not moulted during the prebr moult (GC 1—7) are heavily worn and slightly lighter than in the ad 9 (Fig. 244), and thus of juv plumage.
Fig. 240. Ad 9 after complete postbr moult, 14 September. Whole wing postbr. Whole wing fresh and without moult limits. GC and PC slightly darker than in ly.
Fig. 241. 2y 6 after partial prebr moult, 28 April. MaC mostly prebr. MeC 1-3 postjuv, 4—8 prebr. GC 1—6 juv, 7—10 prebr. Rest of wing juv. The GC not moulted during the prebr moult (GC 1-6) are recognizable as juv by their dark brown, not black colour and their greater abrasion (cf. Fig. 242).
Fig. 242. Ad cT after partial prebr moult, 29 April. MaC mostly prebr, some postbr. MeC and GC postbr. Rest of wing postbr. This ad has not renewed any MeC and GC during the prebr moult. The GC are recognizable as postbr by their blackish colour (cf. Fig. 241). The fringes, however, are worn in this bird.
Fig. 244. Ad 9 after partial prebr moult, 2 May. MaC mostly postbr, some prebr. MeC 1-4 postbr, 5-8 prebr. GC 1—9 postbr, 10 prebr. Rest of wing postbr. The GC not moulted during the prebr moult (GC 1—9) are less worn and slightly darker than in the 2y 9 (Fig. 243), and thus postbr. This difference in wear and colour is less pronounced in 9 than
Fig. 245. 2y <5 after partial prebr moult, 28 April. MaC mostly prebr, some postjuv. MeC 1-3 postjuv, 4-8 prebr. GC 1—3 juv, 4—6 postjuv, 7-10 prebr. T 9 prebr, 7—8 juv. Rest of wing juv. Rare case of a bird with three feather generations within GC. The juv GC 1—3 are dark brown and worn, the postjuv GC 3-6 black-brown as in ad and worn, and the prebr GC 7—10 are fresh. The prebr GC 7 shows the same deep black colour as the prebr MaC and MeC.
104
Oenanthe oenanthe
Oenanthe oenanthe Wheatear Extent of postjuvenile moult MaC: usually all. MeC: usually all. ly with no GC moulted may retain one to four juv MeC.
GC: range 0-5, mean 0.4, mode 0, no GC 71.8% (N=316). T: two birds had T 9 moulted, one T 8 and one T 7 (N=208). The percentage of ly with at least one moulted GC decreases as the autumn migratory season proceeds (Fig. 247). According to Rymkevich (1990), CC, Al and seven to eight GC are not moulted during the postjuv moult.
Fig. 246. Extent of postjuv moult on the wing and tail in ly Oenanthe oenanthe.
Extent of postbreeding moult Usually whole plumage. Among 216 ad, one cT retained S 5 and MeC 2 on the right wing and Al 1, MeC 3 and one MaC on the left wing; another <$ retained Al 1, P 10 and one MaC.
According to our data, the prebr moult on the wing is less extensive than the postjuv moult. Data from spring migrants in Germany (Hantge 1958), indicating a considerably more extensive prebr moult, are difficult to interpret due to unclear feather terminology.
Comments on ageing after postjuvenile and postbreeding moult Best criteria: The colour of the inside of the upper mandible is usually diagnostic. In ly, it is at least partly yellowish, but black in ad. Exceptionally, ly may already have a black inside of upper mandible in autumn (one out of 96). Birds showing a grey inside of upper mandible may be ad or ly. The skull of ly may already be completely pneumatized from mid-August (p. 204); but since there are many ly still showing incomplete pneumatization up to September, it is still worth checking the skull. Plumage characters, mentioned below, are sometimes difficult to apply. ly: Only about 29% show a moult limit within GC, which is usually among the inner GC and sometimes difficult to recognize. Postjuv GC have darker feather centres than juv GC (Fig. 250â&#x20AC;&#x201D;252). ly, especially those with no moult limit within GC, can sometimes (Fig. 250), but not always, be recognized by a difference in colour of the feather centres between the renewed MeC and the juv GC. Ad: ad 2 are difficult to distinguish from ly with no GC moulted. Ad <5 (Fig. 253) can always be recognized by the dark black colour of the whole wing and the greyish, not yellowish-brown outer fringes of the inner GC. Extent of prebreeding moult: 2y and ad MaC: 97.4% moult none, 2.6% some individual MaC (N=188). MeC: 92.7% moult none, 7.3% one to eight MeC (N=179). GC: range 0-2, mean 0.3, mode 0, no GC 78.2% (N=193). T: none 96.4%, one 3.6% (mostly T 9 and sometimes on one wing only)(N=193).
Fig. 247. Percentage of ly Oenanthe oenanthe with at least one postjuv GC during autumn (data grouped in fiveday periods; the first value includes the period 9-28 August, the last 13-22 October).
Fig. 248. Extent of prebr moult on the wing and tail in ad and 2y Oenanthe oenanthe.
Comments on ageing after prebreeding moult Moult limits due to the prebr moult occur in both 2y and ad. Ad 6 are always recognizable by the dark black colour of the whole wing (Fig. 260). The distinction between 2y and ad ?, however, is often problematic. The GC of ad are usually darker and less worn than those of 2y (Fig. 259), but intermediate cases which cannot be aged reliably often occur. Since the prebr moult is slightly less extensive than the postjuv moult, some 2y can be recognized by the moult limit between juv and postjuv GC from last summer (Fig. 256 and 258). 2y having three generations of GC (Fig. 257; 8.3% of 2y, N=193) as well as 2y having three feather generations among MaC, MeC and GC (Fig. 255, 256 and 258) can be aged with certainty.
Oenanthe oenanthe
105
Fig. 252. ly after partial postjuv moult, 29 August. MaC and MeC postjuv. GC 1â&#x20AC;&#x201D;5 juv, 6â&#x20AC;&#x201D;10 postjuv. Rest of wing juv. Rare case of an extensive GC-moult. The moult limit within GC is well marked. The juv GC have brighter brown feather centres and are shorter than the postjuv GC 6-10.
Fig. 249. ly in juv plumage, at the beginning of partial postjuv moult, 10 August. MaC juv, some growing. Rest of wing juv. MaC and MeC with large light tips, typical of juv plumage.
Fig. 250. ly after partial postjuv moult, 19 September. MaC and MeC postjuv. GC 1-9 juv, 10 postjuv. Rest of wing juv. The postjuv GC 10 contrasts with the adjacent juv GC in its darker feather centre and intact fringe. Note also the difference in colour of the feather centres between the postjuv MeC and the juv GC.
Fig. 253. Ad <3 after complete postbr moult, 11 September. Whole wing postbr. Whole wing fresh, wing-coverts and remiges dark black, which is diagnostic of ad 6.
Fig. 251. ly after partial postjuv moult, 10 September. MaC and MeC postjuv. GC 1-8+10 juv, 9 postjuv. Rest of wing juv. The postjuv GC 9 contrasts clearly with the juv GC in its dark black feather centre. Fig. 254. Ad $ after complete postbr moult, 9 September. Whole wing postbr. Ad 9 are often difficult to distingush from ly. Therefore, check colour of inside of upper mandible.
106
Oenanthe oenanthe Fig. 255. 2y 9 after partial prebr moult, 1 May. MaC and MeC postjuv. GC 1-8 juv, 9-10 prebr. Rest of wing juv. Recognizable as 2y by the three feather generations of wingcoverts. The prebr GC 9-10 have dark black feather centres, are hardly worn and contrast with the adjacent very worn and bleached juv GC. The MeC, although worn and bleached, are recognizable as postjuv by being slightly darker than the juv GC 1-8. This bird has very pointed PC, which may give a further indication of 2y.
Fig. 256. 2y 9 after partial prebr moult, 18 April. MaC postjuv. MeC 1—2 juv or postjuv, 3—6 prebr, 7—8 postjuv. GC 1-9 juv, 10 postjuv. Rest of wing juv. Recognizable as 2y by three feather generations of wingcoverts. The postjuv GC 10 is less worn and slightly darker than the juv GC 1-9, but not as dark as the prebr MeC 3-6 (cf. Fig. 255).
Fig. 257. 2y 9 after partial prebr moult, 1 May. MaC and MeC postjuv. GC 10 prebr, 9 postjuv, 1-8 juv. Rest of wing juv. Recognizable as 2y by three feather generations within GC. The fringes of the juv GC 1-8 are almost completely abraded, the fringe of the postjuv GC 9 is still well visible and that of the prebr GC 10 almost intact. The colour of the feather centres is also graduated between the three generations of GC. However, there is almost no di(Terence in colour between the postjuv MeC and the juv GC.
Fig. 258. 2y d after partial prebr moult, 22 April. MaC partly prebr, partly postjuv. MeC postjuv. GC 1—5 juv, 6—10 postjuv. Rest of wing juv. The conspicuous moult limit within GC is due to the postjuv moult and indicates a 2y.
Fig. 259. Ad 9 after partial prebr moult, 2 May. Whole wing postbr. This bird has not renewed any feather on the wing during the prebr moult. The GC are darker and less worn than in 2y.
Fig. 260. Ad <3 after partial prebr moult, 21 April. Whole wing postbr. The dark black colour of the whole wing is diagnostic of ad <$. This bird has no prebr feathers on the wing.
Turdus torquatus
107
Turdus torquatus Ring Ouzel Extent of postjuvenile moult T. torquatus alpestris MaC: all. MeC: usually all. ly with no or few GC moulted may retain up to four
juv MeC. GC: range 0-8, mean 3.6, mode 4, no GC 1.3% (N=227). CC:1.2%(N=163). T: one bird with four postjuv GC renewed T 8+9 (N=l62). T. torquatus torquatus MaC and MeC: all. GC: range 2-7, mean 3.9, mode 4 (N=60); not significantly different from T. t. alpestris.
Fig. 261. Extent of postjuv moult on the wing and tail in ly/2y Turdus torquatus alpestris.
In T. t. alpestrisy there is no significant difference in the extent of postjuv moult between the sexes nor a trend with season. Extent of postbreeding moult (both subspecies) Whole plumage. Exceptionally, single feathers may be retained (Fig. 269). Comments on ageing (both subspecies) Best criteria: Moult limit within GC usually diagnostic of ly/2y. ly/2y with no GC moulted recognizable by distinct tips on innermost GC. Skull pneumatization until at least the end of October (p. 205). ly/2y: 98.7% show a moult limit within GC which is usually easily recognizable. Juv GC are brown, sometimes tinged bronze, with a buffish fringe and tip on outer web which bleaches during summer and is off-white in autumn (cf. Fig. 264-265 with 266-267), The pale tips vary in extent between individuals and may be virtually absent on outer juv GC (cf. Fig. 263 and 264). Postjuv GC are tinged grey, have a greyish to greyish-white outer fringe and no distinct pale tips. Often, postjuv GC show growth bars (e.g. GC 9 in Fig. 265). ly/2y with no GC moulted (1.3%) are easily recognized by pale tips on innermost GC extending to the shaft. Ad: No moult limit within GC, All GC, Al and CC have a greyish, not buffish or off-white outer fringe and no distinct tips.
Fig. 263. ly T. t. alpestris at the beginning of partial postjuv moult, 6 August. MaC partly juv, partly postjuv. Rest of wing juv. Juv MaC and MeC with broad buffish shaft streaks, typical of juv plumage. Inner GC with buffish tips extending to the shaft, outer GC with distinct tips on outer web.
Fig. 262. Extent of postjuv moult on the wing and tail in ly/2y Turdus torquatus torquatus. Fig. 264. ly T. t. alpestris at the beginning of partial postjuv moult, 4 August. MaC partly juv, partly postjuv. Rest of wing juv. This bird has only narrow shaft streaks on juv MaC and MeC. Only GC 10 has a distinct tip, the others at most a small terminal dot.
Fig. 265. ly T. t. alpestris after partial postjuv moult, 5 September. MaC and MeC postjuv. GC 1-8 juv, 9â&#x20AC;&#x201D;10 postjuv. Rest of wing juv. Distinct moult limit within GC. Postjuv GC 9-10 tinged grey and with greyish outer fringe. Juv GC brown with off-white outer fringe and distinct tips on GC 6-8.
108
Turdus torquatus
Fig. 266. ly 9 T.t. torquatus after partial postjuv moult, 28 October. MaC and MeC postjuv. GC l_7 + 10juv,8-9 postjuv. Rest of wing juv. Recognizable as ly by moult limit within GC. Postjuv GC 8-9 tinged grey with greyish outer web, juv GC with offwhite outer web. GC 10 is juv because of the distinct pale tip. Fig. 267. ly 9 T.t. alpestris after partial postjuv moult, 5 October. MaC and MeC postjuv. GC 1-5 juv, 6â&#x20AC;&#x201D;10 postjuv. Rest of wing juv. Conspicuous moult limit within GC. Postjuv GC tinged grey with greyish outer fringe, juv GC brown with off-white outer fringe.
Fig. 268. Ad 9 T. t. alpestris after complete postbr moult, 11 October. Whole wing postbr. All GC, Al and CC with greyish outer fringe and no distinct triangular tips. Growth bars on inner S at different levels.
Fig. 269. Ad d T. t. torquatus after complete postbr moult, 8 October. Whole wing postbr except GC 10. No moult limit within GC. Outer greyish fringes on GC narrow and only present near the tip. GC 10 has been retained and is heavily bleached.
Turdus merula
109
Turdus merula Blackbird Extent of postjuvenile moult
MaC: all. MeC: all, except one bird which retained two juvMeC (N=611). GC: range 1-10, mean 6.9, mode 7, all GC 10.9% (N=1068). CC: 61.8%. Al: none 71.3%, one 27.8%, two 0.9% (N=995). T: none 76.1%, one 9.9%, two 8.2%, three 5.8% (N=891) (see p. 33). R: none 96.9%, one 1.5%, two 0.9%, three 0.3%, four 0.3% (N=337). S, P and PC: In an urban winter roost in Switzerland (Richter 1972), 8.2% (N=525) showed one to five replaced S, usually together with all GC and some T. S 6 is renewed most frequently (42% of those with moulted S; see also Gurr 1954). Mostly, S are replaced asymmetrically and in irregular sequence. Exceptionally, individual P and PC were renewed (details see Richter 1972). Possibly, the replacement of P, PC and individual outer S is due to accidental feather loss. The extent of postjuv moult is correlated among GC, CC, Al, T and R (Fig. 271; see also Baillie & Swann 1980). T may be renewed when at least four GC are moulted, Al 1 and CC when at least five and R when at least eight GC are moulted. The data presented above include wintering birds examined by Richter (1972). There were no significant differences in the number of moulted GC between the sexes, as also found by Baillie & Swann (1980). In Switzerland, the number of GC moulted decreases as the autumn migratory season proceeds (Fig. 272). The extent of postjuv moult is lowest in migratory birds during autumn on Col de Bretolet (GC mean 6.9, CC 51%, Al 1 18.4%, one Fig. 271. Relationships between the number of postjuv GC and the percentage of individuals with renewed CC, Al, T and Rin ly/2y Turdus merula which have completed their postjuv moult (including data from Richter 1972).
Fig. 270. Extent of postjuv moult on the wing and tail in ly/2y Turdus merula including data from Richter (1972) of a Swiss winter roost. S, P and PC see also text.
to three SF 19%; N=201), intermediate in birds wintering near Basel (6.9, 64%, 31%, 27%, respectively; N=611; Richter 1972) and highest in spring birds (April, May) in S Switzerland (7.0, 77%, 39%, 21%, respectively; N=87, see also Fig. 272). Birds wintering in Scotland have a less extensive postjuv moult than all birds examined further south (Baillie & Swann 1980): in a Scottish rural roost, the number of GC moulted was particularly low (mean 6.3, N=357; re-calculated on the basis of ten GC), probably due to northern immigrants, while birds in Scottish urban roosts moulted on average 6.7 GC (N=1670), 39% the CC and 1.4% Al 1 (N=143). A more extensive postjuv moult was found in birds wintering in S England (GC mean 7.7, N=108; Baillie & Swann 1980), in birds from Germany (all year, mean 7.9 GC, 35% at least one T; N=80; Sommerfeld 1930) and in birds from New Zealand (mean 8.2 GC, 60% at least one T; N=29; Gurr 1954). All GC are moulted more frequently in Britain and Central Europe than in Scandinavia (Svensson 1992). Extent of postbreeding moult Whole plumage. Exceptionally, temporarily halted P-mouIt occurs (Herroelenl980). Prebreeding moult There are indications of a possible prebr moult (Witherby et aL 1943, Gurr 1954, Glutz & Bauer 1988, Svensson 1992) which may comprise part of the body-feathers. However, there are no detailed accounts on its extent and timing (in New Zealand only ly/2y; Gurr 1954). We found a small number of growing body-feathers only in a very few winter and spring birds. It remains unclear whether or not this represents a true moult. Comments on ageing Best criteria: Moult limits within GC, Al, T and between GC, CC, Al and PC diagnostic of ly/2y. Skull pneumatization until November (p.
205).
Fig. 272. Mean number of postjuv GC in the course of the year of ly/2y Turdus merula which have completed the postjuv moult (September until early November: five-day periods, the last value includes the period 23 October-6 November). Data labelled Nov. - March are from a city roost (Richter 1972).
ly/2y: 89% show a moult limit within GC which is easy to recognize up to the second summer in both sexes (Fig. 274 and 275). Juv GC are distinctly browner than postjuv GC and the innermost juv GC often have a pale shaft streak (Fig. 273). ly/2y with all GC moulted (Fig. 276) usually have a renewed CC and Al 1 and show a contrast between the juv PC and the postjuv GC, Al 1 and CC. Moult limits within T and between T and S are diagnostic as well.
110
Turdus merula
Ad: No moult limit within GC, T and Al and between PC and GC, CC and Al. T of the same colour as S (Fig. 277 and 278). R usually more rounded than in ly/2y, but some may be moulted in ly/2y, thus showing the shape of ad.
Fig, 273. ly in juv plumage, 21 July. Whole wing juv. MaC and MeC show pale shaft streaks, typical of juv plumage. All GC brownish, innermost with pale tips extending to the shaft.
Fig. 276. 2y 9 after partial postjuv moult, 11 April. MaC and MeC postjuv. GC postjuv. CC and Al 1 postjuv, 2-3 juv. T 7 juv, 8-9 postjuv. Rest of wing juv. Recognizable as 2y by the difference in colour between the dark postjuv GC, Al 1 and CC and the slightly paler and browner juv PC. Note also the moult limit within T.
Fig. 274. 2y <J after partial postjuv moult, 7 April. MaC and MeC postjuv. GC 1â&#x20AC;&#x201D;4 juv, 5-10 postjuv. T 7-8 juv, 9 postjuv. Rest of wing juv. Moult limit within GC diagnostic of 2y. Juv GC are distinctly browner than postjuv GC.
Fig. 275. ly $ after partial postjuv moult, 30 November. MaC and MeC postjuv. GC 1-2 juv, 3-10 postjuv. CC postjuv. Rest of wing juv. Conspicuous moult limits within GC and between the postjuv CC and the juv PC and Al.
Fig. 277. Ad 9 after complete postbr moult, 23 April. Whole wing postbr. Almost no difference in colour between GC, CC, Al and PC and between T and S.
Fig. 278. Ad 6" after complete postbr moult, 30 September. Whole wing postbr. Whole wing uniformly deep black.
Turdus pilaris
111
Turdus pilaris Fieldfare Extent of postjuvenile moult MaCandMeGall. GC: range 2-8, mean 4.9, mode 5 (N=133). CC: 2.2%. Al: none 97.8%, one 2.2% (N=93). T: none 93.4%, one 2.2%, two 3,2%, three 1.1% (N=94). R: one bird renewed R 1 (N=94). There are no significant differences in the number of GC moulted between the sexes. The extent of postjuv moult decreases as the autumn migratory season proceeds and is lowest during winter (Fig. 280). Birds from E Austria and Heligoland (Lidauer 1983) moulted on average 4.9 GC (range 2-8, N=74) and 8.2% from E Austria moulted the CC and one bird Al 1 (N=62). In NW Russia, usually five GC are moulted (Rymkevich 1990). In caged birds, moult of R (Heinroth & Heinroth 1926) and part of wing-feathers (Liibcke & Furrer 1985) was observed, which might be an artefact due to captivity.
Fig. 279. Extent of postjuv moult on the wing and tail in ly/2y Turdus pilaris.
Extent of postbreeding moult Whole plumage. Comments on ageing Best criteria: Skull pneumatization until at least November, possibly up to December (p. 205). Moult limit within GC diagnostic of ly/2y although sometimes difficult to recognize. R usually more pointed in ly/2y than in ad. ly/2y: According to the present data, all ly/2y show a moult limit within GC which is usually distinct (Fig. 282, 283 and 285), but sometimes difficult to recognize (Fig. 284). Juv GC show individually variable white or light grey tips and outer fringes, the innermost GC have a white shaft streak (Fig. 281). Postjuv GC show no white tips, but greyish terminal fringes and brownish outer webs. Until spring, the fringes and tips of GC may be abraded and juv GC can only be recognized by their slightly duller colour and sometimes shorter length. R usually more pointed and narrower than in ad (see Svensson 1992). Ad: GC without moult limit, light outer fringe, white tips or white shaft streaks.
Fig. 280. Mean number of postjuv GC in the course of the year of ly/2y Turdus pilaris which have completed the postjuv moult.
Fig. 281. ly in juv plumage, 12 July. Whole wing juv. MaC, MeC and inner GC with pale shaft streaks over the whole feather length, typical of juv plumage.
Fig, 282. ly after partial postjuv moult, 26 October. MaC and MeC postjuv. GC 1-6 juv, 7â&#x20AC;&#x201D;10 postjuv. Rest of wingjuv. Conspicuous moult limit within GC. Juv GC with white tips and narrow ofF-white outer fringes, shorter and duller than postjuv GC. Postjuv GC with greyish terminal fringes and brown outer fringes.
Fig. 283. 2y after partial postjuv moult, 31 January. MaC and MeC postjuv. GC 1â&#x20AC;&#x201D;5 juv, 6-10 postjuv. Rest of wing juv. Distinct moult limit within GC. Juv GC without brown and with light grey outer fringes, slightly shorter than postjuv GC.
112
Turdus pilaris Fig. 284. ly after partial postjuv moult, 26 October. MaC and MeC postjuv. GC 1—4 juv, 5—10 postjuv. Rest of wing juv. Moult limit within GC difficult to recognize. The light outer fringe and tip on GC 1—4, typical of juv GC, is only very faint.
Fig. 285. ly after partial postjuv moult, 30 August. MaC and MeC postjuv. GC 1-2 juv, 3—10 postjuv. CC postjuv. Rest of wing juv. GC 1—2 recognizable as juv by whitish terminal fringes and by less brown outer webs. Postjuv CC greyish as adjacent MaC.
Fig, 286. Ad cT after partial postbr moult, 19 October. Whole wing postbr. All GC deeply coloured, without light outer fringes and tips.
Turdus philomelos
113
Turdus philomelos Song Thrush Extent of postjuvenile moult
MaC: all. MeC: usually all. ly/2y with no GC moulted may retain individual juv MeC GC: range 0-9, mean 3.9, mode 3, no GC 0.8% (N=l 103). CC: 3.5%. Al: none 96.7%, one 3.1%, two 0.2% (N=764). T: none 98.4%, one 0.8%, two 0.7%, three 0.1% (N=756). R: no birds were found to renew R, except irregular replacement of accidentally lost R (N=755). The extent of postjuv moult is correlated among GC, CC and Al (Fig. 288). Al 1 may be renewed when at least three, CC when at least four GC are moulted. The extent of postjuv moult decreases markedly as the autumn migratory season proceeds (Fig. 289). Autumn migrants in NE Spain moulted on average 2.9 GC (range 0-8, N=686) out of GC 1-9 (Aymi 1990), which corresponds closely with our data assuming that GC 10 is usually moulted. In England, ly with all GC and some R moulted were found exceptionally (Spencer & Mead 1978a, Ginn & Melville 1983, Roselaar in Cramp 1988). Extent of postbreeding moult Whole plumage. One bird was observed to suspend P-moult after renewal of P 1-2 (Herroelen 1980), possibly in the context of another breeding attempt. Comments on ageing Best criteria: Moult limit within GC usually diagnostic of ly/2y. ly/2y with no GC moulted recognizable by shaft streaks on innermost GC. Skull pneumatizadon until mid-October, but many ly have incomplete pneumatization until winter (p. 205).
Fig. 288. Relationships between the number of postjuv GC and the percentage of individuals with renewed CC and Al in ly/2y Turdus pbilomelos which have completed their postjuv moult.
Fig. 289. Mean number of postjuv GC in the course of the year of ly/2y Turdus pbilomelos which have completed the postjuv moult (September until November: five-day periods; the first value includes the period 30 July-2 September).
Fig. 287. Extent of postjuv moult on the wing and tail in ly/2y Turdus philomelos.
ly/2y: 99.2% show a moult limit within GC, recognizable by an abrupt change in the shape of the light tips within the row of GC and by differences in colour of the feather centres. Moult limits among inner GC are conspicuous (Fig. 292 and 293). Inner juv GC have large pale tips extending to the shaft, inner postjuv GC show none or only small tips. Moult limits among the outer four GC are more difficult to recognize, since the difference in shape of the pale tips on GC is less marked (Fig. 294 and 295). Usually, juv GC have rusty-yellowish tips, postjuv GC yellowish tips. The few birds with no GC moulted are easily recognized by the shaft streaks on the innermost GC (Fig. 291). In order to recognize moult limits, the colour of the feather centres of GC is as important as the shape of the tips. Juv GC (and PC) have a rusty tinge, postjuv GC an olive tinge. In British birds, this difference in colour between the two generations of GC is apparently less marked (Svensson 1992). As an auxiliary criterion, the shape of the R may be helpful, although not all birds can be aged by this. The R (especially R 1) of ly/2y are usually more pointed and narrower than in ad. Birds having a light tip or terminal fringe on the CC are ly/2y, those without can be either ad or ly/2y with a renewed CC or ly/2y with no light tip on juv CC (7%). Ad: No moult limit within GC. Pale tips on GC on average smaller than in 1 y/2y and never extending to the shaft. R, especially R 1, less pointed and broader than in ly. CC without pale tip.
Fig. 290. ly in juv plumage, 10 July. Whole wing juv. MaC, MeC and inner GC with shaft streaks, typical of juv plumage.
114
Turdus philomelos Fig. 291. ly after partial postjuv moult, 11 October. MaC postjuv. MeC 1-3+5-8 postjuv, 4 juv. GC and rest of wing juv. One of the few ly with no GC moulted. Easily recognizable by the juv MeC 4 and the inner GC having conspicuous shaft streaks over the whole feather length.
Fig. 292. ly after partial postjuv moult, 1 October. MaC postjuv. MeC postjuv. GC 1-8 juv, 9-10 postjuv. Rest of wing juv. Distinct moult limit within inner GC. Postjuv GC 9-10 with an olive tinge and without pale tips, inner juv GC with a rusty tinge and with large tips extending to the shaft.
Fig. 295. ly after partial postjuv moult, 17 September. MaC postjuv. MeC postjuv. GC 1+3 juv, 2+4—10 postjuv. CC postjuv. Al 1—2 postjuv, 3 juv. T 7-9 postjuv. Rest of wing juv. Exceptional case of a ly with all T renewed. Juv GC 1+3 recognizable by the rusty tinge. Renewed GC, T, CC and Al 1—2 tinged olive.
Fig. 293. 2y after partial postjuv moult, 7 April. MaC postjuv. MeC postjuv. GC 1-6 juv, 7-10 postjuv. Rest of wing juv. The moult limit within GC is still conspicuous in spring.
Fig. 296. Ad after complete postbr moult, 30 September. Whole wing postbr. No moult limit within GC. Small tips of GC without abrupt change in shape. PC tinged olive. Fig. 294. ly after partial postjuv moult, 11 September. MaC postjuv. MeC postjuv. GC 1-3 juv, 4-10 postjuv. CC postjuv. Al 1 postjuv, 2-3 juv. T 7-8 juv, 9 postjuv. Rest of wing juv. Moult limit among outer GC recognizable by a discontinuity in the shape of the pale tips over the row of GC and by a difference in colour. Juv GC 1-3, Al 2-3 and PC tinged rusty, postjuv GC 4-10, CC and A l l tinged olive.
Fig. 297. Ad after complete postbr moult, 7 April. Whole wing postbr. Wear until spring is not very marked and usually allows ageing with the same criteria as in autumn.
Turdus iliacus
115
Turdus iliacus Redwing Extent of postjuvenile moult
MaCandMeQall.
GC: range 2-10, mean 4.7, mode 5, all GC 3.1% (N=64). Al: one bird had Al 1 renewed (N=4l). T: one bird had T 8-9 renewed (N=64). According to Riddiford (1981) and Svensson (1992), some birds may renew all GC, T and R 1 during the postjuv moult. Rymkevich (1990) reports from NW Russia that GC and Al may remain unmoulted or partially moulted and that most ly renew five GC. Fig. 298. Extent of postjuv moult on the wing and tail in ly/2y Turdus iliacus.
Extent of postbreeding moult Whole plumage. Comments on ageing Best criteria: Moult limit within GC usually diagnostic of ly. ly with fully pneumatized skulls appear from the beginning of October. ly/2y: Most birds show a moult limit within GC which is still easily recognized in spring (Fig. 300). Juv GC show whitish or yellowish tips which are very small or absent on the outermost GC, but conspicuous and shaped like a shaft streak on the innermost GC (Fig. 299). Postjuv GC show no light tips, but sometimes narrow light fringes. A moult limit within GC is recognized by an abrupt change in the shape of the light tips. The juv GC are often shorter than the postjuv. The tips on juv T 8 and 9 are variable and can be used as a supplementary criterion only. Often, juv T 8 and 9 have a small white triangular tip (Fig. 301), indicative of ly/2y. Some ly/2y, however, show only a light fringe (T 8 in Fig. 299).
Fig. 300. 2y after partial postjuv moult, 1 April. MaC and MeC postjuv. GC 1-7 juv, 8-10 postjuv. Rest of wing juv. Moult limit within GC still recognizable in spring. Renewed GC without light tips and slightly tinged greenish.
Ad: All GC and T without light tips. Some may have narrow light fringes at the tip (Fig. 302).
Fig. 301. ly after partial postjuv moult, 12 November. MaC and MeC postjuv. GC 1â&#x20AC;&#x201D;6 juv, 7â&#x20AC;&#x201D;10 postjuv. Rest of wing juv. Postjuv GC without light tips and tinged greenish.
Fig. 299. ly after partial postjuv moult, 31 October. MaC and MeC postjuv. GC 1-8 juv, 9-10 postjuv. Rest of wing juv. Recognizable as ly by the moult limit within GC. Postjuv GC 9-10 without light tips and longer than juv GC.
Fig. 302. Ad after complete postbr moult, 2 November. Whole wing postbr. All GC and T without light tips, T 8 and 9 with narrow light fringes.
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Turdus viscivorus
Turdus viscivorus Mistle Thrush Extent of postjuvenile moult MaC and MeC: usually all. ly/2y with few renewed GC may retain individual MaC and MeC. GC: range 0-9, mean 4.5, mode 6, no GC 8.3% (N=48). Al, CC, T: two birds renewed Al 1 and T 8—9 besides eight GC, one of these also the CC (N=42). Exceptionally, all GC may be moulted (Svensson 1992). Extent of postbreeding moult Whole plumage.
Fig. 303. Extent of postjuv moult on the wing and tail in ly/2y Turdus viscivorus.
Comments on ageing Best criteria: Usually, moult limits within MaC, MeC and GC diagnostic of ly/2y, but sometimes difficult to recognize, especially in spring, ly not fully pneumatized during October (N=23). Skull pneumatization difficult to recognize in live birds due to the thickness of the scalp. ly/2y: The extent and shape of the white tips on GC are very variable between individuals and feather generations. Both juv (Fig, 304) and postjuv (Fig. 306) GC may be conspicuously tipped whitish. Moult limits within GC are best recognized by differences in the colour of the outer fringe between juv and postjuv GC or by an abrupt change in the shape of the light tips over the row of GC. Very fresh juv GC have huffish outer fringes (Fig. 304) which soon bleach to greyish-white in autumn, while outer fringes of postjuv GC are buffish. Juv GC are often shorter than postjuv ones (Fig. 305 and 307). Juv MaC, MeC or GC 8—10 are, if not moulted, easily recognizable by their conspicuous shaft streaks (Fig. 304). In spring, the outer fringes of GC are often completely abraded and moult limits are difficult to recognize, mostly by differences in length and bleaching of the two generations of GC (Fig. 307). As a supporting criterion, the shape of the R may be used. In ly/2y they are narrower and more pointed than in ad.
Fig. 305. ly after partial postjuv moult, 30 September. MaC and MeC postjuv. GC 1—6 juv, 7-10 postjuv. Rest of wingjuv. Recognizable as ly by the moult limit within GC. Juv GC with whitish, postjuv GC with buffish outer fringes. The shape of the light tips on GC changes abruptly at the moult limit. Juv GC shorter than postjuv.
Ad: All GC with buffish outer fringe. No abrupt change in the shape of the light tips over the row of GC. R usually broader and less pointed than in ly/2y.
Fig. 304. ly in juv plumage, 1 August. MaC, MeC and GC 10 with conspicuous white shaft streaks over the whole feather-length.
Fig. 306. ly after partial postjuv moult, 14 October. MaC and MeC postjuv. GC 1-2 juv, 3-10 postjuv. Al 1 postjuv, 2-3 juv. T 7 juv, 8-9 postjuv. Rest of wing juv. Postjuv GC fringed huffish, juv GC 1—2 fringed white and more bleached. Since the moult limit is among the outer GC, there is no conspicuous change in the shape of the light tips between renewed and juv GC. Note also the moult limit within Al and T.
Turdus viscivorus Fig. 307. 2y after partial postjuv moult, 12 April MaC and MeC postjuv. GC 1-5 juv, 6-10 postjuv. Rest of wing juv. The outer fringes of GC are completely abraded and cannot be used for ageing, but the moult limit within GC is still recognizable: juv GC are shorter than postjuv and more bleached to dark brown without greyish tinge.
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Fig. 308. Ad after complete postbr moult, 8 October. Whole wing postbr. All GC with buffish outer fringes. The light tips on GC change gradually along the row ofGC.
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Acrocephalus scirpaceus
Acrocephalus scirpaceus Reed Warbler Extent of postjuvenile moult MaC and MeC: since juv and postjuv MaC and MeC are difficult to separate after the postjuv moult, we have no data on the proportion of juv feathers retained. According to Rymkevich (1990) and own observations on birds in moult, MaC and MeC are at least partly renewed. GC: range 0-6, mean 0.2, mode 0, no GC 84.8% (N=474). R: rarely, some R are replaced, probably due to accidental loss. In NW Russia, most birds renew the body-feathers, but rarely the upper- and undertail-coverts; 20% (N=57) of ly from the Finnish Bay moult part of GC, MaC, MeC, but only 6% (N=102) of ly in Ladoga (Rymkevich 1990). In England, about 90% of ly renew a large proportion of the body-feathers and about 30% show 'wing-covert moult' (Tyson & Pepler 1976). According to Herremans (1990b), most ly migrants in Belgium, at least of the northern populations, undergo only a slight and irregular moult of body-feathers before and during the departure to the wintering grounds. A continuation of body moult during migration through Europe is also suggested by Tyson & Pepler (1976). Extent of postbreeding moult Body-feathers, MaC and MeC are only partly renewed. 6% of ad renew one to seven, mostly inner, GC and 5% one to three T (N=80). According to Herremans (1990b), a postbr moult in the breeding area may be completely suppressed. Rymkevich (1990), however, recorded a partial body-feather moult in all ad, especially on head, nape, breast, shoulders and tail-coverts, rarely on back and belly; four birds renewed some inner GC. In England, the proportion of ad actively moulting body-feathers and 'wing-coverts* is smaller than in ly (Tyson &: Pepler 1976). Replacement of individual R was recorded in England which may be due to accidental loss (Ginn & Melville 1983). According to Spencer & Mead (1979), some ad have been recorded moulting completely in Spain, but this remains inconclusive and may concern moult interruption. Comments on ageing after postjuvenile and postbreeding moult Best criteria: Skull pneumatization until at least November (p. 205). Pronounced difference in wear of wing-feathers and coverts, especially T, between ly and ad.
Fig. 309. Extent of postjuv moult on the wing and tail in 1 y Ac rocephalus scirpaceus.
spots) and tarsus usually pale flesh coloured (Crudass & Devlin 1967, Kuschert 1980, Karlsson etal 1988). Extent of prebreeding moult: 2y and ad Whole plumage. There is a large variation in the timing of the complete moult in Africa. In W Africa, all birds seem to moult mainly between September and November/early December (Aidley & Wilkinson 1987, Bensch et at. 1991). In the eastern part of Africa, many birds (ly/2y and ad) moult somewhere in NE Africa during autumn and may continue migration afterwards towards the south. Others (ly and ad) moult in central eastern Africa between October and April or in the southern part of Africa from January onwards (Pearson 1972, 1973, 1982, Hanmer 1979, Dowsett-Lemaire & Dowsett 1987); birds still in old plumage were recorded in January and end of February in Namibia (Komen & Myer 1988, van den Brink & Loske 1990). Moult may be suspended while in Africa (Pearson 1973, Hanmer 1979, Renschetal. 1991). Birds moulting in early winter may perform an additional partial moult of body-feathers and wing-coverts before spring migration (Roselaar in Cramp 1992). Comment on ageing after the prebreeding moult Ageing according to plumage characters not possible. Many birds can be aged according to slight differences in colour of iris, tarsus and tongue spots (see Karlsson etal. 1988 for details).
ly: Whole plumage fresh, distincly less worn than in ad. Fringes of all GC and T without strong signs of abrasion (Fig. 310). 15%of lyshow a moult limit within GC which is easily recognized (Fig. 311), but show a less conspicuous contrast in wear than in those ad renewing GC. Colour of iris, tarsus and tongue spots may be used as additional criteria. Birds with dark grey iris, black tongue spots and greyish blue tarsus are ly (Crudass & Devlin 1967, Kuschert 1980, Karlsson et al. 1988). According to Karlsson et at. (1988), ly and ad can always be separated by iris colour, but not according to Kuschert (1980). Birds with faint tongue spots may be ad or ly as well as birds with bluish tinged tarsi (Crudass & Devlin 1967, Kuschert 1980, Karlsson et at. 1988). Ad: Plumage markedly worn and bleached. Wear is most pronounced on MeC, GC and T (Fig. 312). About 5-6% renew some GC or T and show a distinct moult limit (Fig. 313). These ad are easily distinguished from ly with moult limits by the adjacent worn unmoulted feathers. Iris colour usually brown, tongue spots absent (some ad have faint
Fig. 310. ly after partial postjuv moult, 16 August. MaC and MeC juv or postjuv. GC and rest of wing juv. Recognizable as ly by the completely fresh and hardly worn wing. All GC loosely textured.
Acrocephalus scirpaceus Fig. 311. 1 y after partial postjuv moult, 28 August. MaC and MeC juv or postjuv. GC 1â&#x20AC;&#x201D;6 juv, 7-9 postjuv, 10 hidden. Rest of wing juv. Recognizable as ly by the intact GC and T. The renewed GC are longer, more firmly textured and slightly darker than the juv GC, The moult limit is less conspicuous than in those few ad showing renewed GC.
Fig. 312. Ad after partial postbr moult, 6 August. Whole wing prebr. Recognizable as ad by the worn wing, especially marked on GC, T and tips of P. During the postbr moult, no feathers of the wing have been renewed.
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Fig. 313. Ad during partial postbr moult, 29 August. Inner MaC partly postbr, rest prebr. MeC prebr. GC 1+8+10 prebr, 2-7 postbr, 9 growing. Rest of wing prebr. The renewed GC are distinctly darker and less worn than the prebr GC. In contrast to ly showing a moult limit within GC, the moult limit is more conspicuous and the retained GC, T and P are markedly worn.
Fig. 314. 2y/ad after complete prebr moult. 7 May. Whole wing prebr. After the complete prebr moult in the winter quarters, ageing according to plumage characters is no longer possible.
Hippolais icterina Icterine Warbler Extent of postjuvenile moult MaC and MeC: many moult all, some part or none (Fig. 317). The latter include birds with predominantly juv body plumage during migration. GC: range 0-2, mean 0.2, mode 0, no GC 83.9% (N=87). According to Rymkevich (1990), the completion of the juv plumage and the postjuv moult are difficult to separate and ly may moult only part of the body-feathers or none at all. According to Roselaar (in Cramp 1992; see also Heinroth & Heinroth 1926), there is no moult before autumn migration, but only a completion of the juv plumage. However, according to our data, some ly replace some body-feathers and wing-coverts.
Fig. 315. Extent of postjuv moult on the wing and tail in ly Hippolais icterina.
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Hippolais icterina
Extent of postbreeding moult The postbr moult is of very limited extent and includes only part of the body-feathers. Ad may migrate while body-feather moult still in slow progress. According to Rymkevich (1990), ad moult less than half of the body-feathers, about a third of the ad the tail-coverts and very few the innermost MeC. Roselaar (in Cramp 1992) reports a very restricted or completely suppressed moult before autumn migration. Comments on ageing after postjuvenile and postbreeding moult Best criteria: Skull pneumatization until at least the end of September (p. 205). Pronounced difference in wear of wing-feathers and coverts, especially T. ly: Wing-feathers and wing-coverts only slightly worn and bleached. T with fresh intact fringes (Fig. 316). Ad: Wing-feathers and wing-coverts considerably more worn and bleached than in ly, especially conspicuous on fringes of T which are tattered in ad (Fig. 318).
Fig. 318. Ad after partial postbr moult, 10 August. Whole wing prebr. All feathers considerably worn.
Extent of prebreeding moult: 2y and ad Whole plumage (205 spring migrants in Italy from the first half of May). Birds arriving in Europe show differences in wear between individuals (cf. Fig. 319 and 320). Ageing on plumage after the prebr moult is not possible. Fig. 319. 2y/ad after complete prebr moult, 2 May. Whole wing prebr. Example of a bird with a relatively fresh plumage on arrival in Europe.
Fig. 316. ly after partial postjuv moult, 18 September. MaC and MeC postjuv. GC 1-9 juv, 10 postjuv. Rest of wing juv. Whole plumage fresh and hardly worn. Fringes of T intact. The renewed GC 10 is slightly darker and glossier than the juv GC.
Fig. 317. ly after partial postjuv moult, 14 August. Proximal MaC postjuv, rest juv. MeC, GC and rest of wing juv. Recognizable as ly by the fresh plumage. This bird had undergone a postjuv moult of very limited extent.
Fig. 320. 2y/ad after complete prebr moult, 28 April. Whole wing prebr. Example of a bird with a relatively worn plumage on arrival in Europe. The protected GC 10 and CC look much fresher, but are also prebr.
Sylvia curruca
121
Sylvia curruca Lesser Whitethroat Extent of postjuvenile moult
MaC and MeC: all. GC: range 3-10, mean 8.3, mode 9, all GC 24.2% (N=95). CC: 15.8%. Al: none 40.4%, one 57.9%, two 1.8% (N=57). T: none 90.0%, one 3.3%, two 5.0%, three 1.7% (N=60). R: one bird had R 1 growing and another R 1 renewed. CC, Al and T may be renewed when at least seven GC are moulted, ly in August had significantly more renewed GC (mean 9.1, N=45) than ly during September (mean 7.7, N=49). In Sweden and England, a small percentage renewed some or all R (Norman 1990a, Svensson 1992) and in England, replacement of S was found (Norman 1990a). In NW Russia, moult of part or all bodyfeathers and MaC, all MeC, five to ten GC, sometimes R, but not CC, Al and T was observed (Rymkevich 1990). According to this author, early-hatched birds renew all GC, late-hatched five to eight. Extent of postbreeding moult Whole plumage. Rymkevich (1990) observed rare cases of ad retaining Al and one to three innermost S. Comments on ageing after postjuvenile and postbreeding moult Best criteria: Skull pneumatization until at least the beginning of October (p. 205). Moult limits within GC, Al and between CC, Al and PC diagnostic of ly. ly: 76% show a moult limit within GC, mostly among the outer GC. Postjuv GC have greyish feather centres and grey outer fringes, juv GC show brownish feather centres and brown outer fringes, ly with all GC renewed always have a renewed Al 1, thus showing a contrast between the greyish fringed postjuv Al 1 and the brownish fringed juv Al 2-3 (cf. Fig. 322, 324, 325). Birds with a renewed CC (16%) show a contrast between the grey fringe of the renewed CC and the brownish juv PC (Fig. 38, p. 51). Ad: No moult limit within GC and Al, nor between CC and PC. R 6 usually with pure white parts at tip, R 5 broadly tipped white. In ly, R 6 tinged brownish and R 5 without white tip. Since some birds show transitions between typical ad and typical ly R-patterns, this may be used as a supporting criterion only. For differences in iris colour between ad and ly see Svensson (1992).
Fig. 321. Extent of postjuv moult on the wing and tail in ly Sylvia curruca.
certainly some 2y). S 5, S 5-6 and S 4-6 were renewed in three, single birds, and S 1-6 in two ad (N=40). One bird with S 4-6 growing showed clearly that the S were shed from inside to outside (descendantly). P: one bird was found with P 5 renewed on one wing, another bird with a new P 1 on one wing only. 15% of Swedish spring birds moulted part or all R (J. Pettersson in Svensson 1992). Prebr moult of part of the R was also reported by Mathiasson (1971) and Aidley & Wilkinson (1987). Roselaar (in Cramp 1992) reports that the prebr moult may be entirely suppressed. However, the amount of wear of prebr feathers in spring is variable and can be considerable which may lead to an underestimation of the extent of prebr moult. As in other members of the genus Sylvia, the prebr moult seems to be more extensive and complex than hitherto reported. Comments on ageing after prebreeding moult Ageing spring birds is very difficult. The criterion given for autumn birds based on the coloration of the outer R is no longer valid due to wear and prebr renewal of R. With experience, some spring birds may be aged on the degree of abrasion and wear of the PC. In ad, PC are usually darker and considerably less worn than in 2y which show more pointed and worn PC (cf. Fig. 328 with Fig. 326 and 327).
Extent of prebreeding moult: 2y and ad As in S. communis, the distinction between feather generations in spring is sometimes problematic due to individual differences in wear. Therefore, the following account, mainly based on skins from the British Museum (Natural History), is probably incomplete. MaC and MeC: completely, partly or not at all renewed. GC: range 0-4, mean 1.8, mode 0, no GC 70.0% (N=40). Whether or not birds with all GC renewed occur, remains to be discovered. Al: Al 1 is moulted by about 50%. T: usually all. Rarely, one or two T remain unmoulted. Whether or not birds with no T moulted occur remains open, because of large differences in wear. R: about 50% moult none, the others mostly R 1, rarely two to four R and in one bird all six R (N=33). S: 37.5% renew one to six S, most frequently S 6 (22.5%, among them
Fig. 322. ly after partial postjuv moult, 24 August. MaC postjuv. MeC postjuv. GC 1 juv, 2-10 postjuv. Al 1 postjuv, 2-3 juv. Rest of wing juv. Moult limit within GC. Juv GC 1 with brownish outer fringe and less greyish feather centre than postjuv GC 2-10 fringed greyish. Postjuv Al 1 fringed grey as the postjuv MaC and MeC. Juv CC fringed brown as GC 1.
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Sylvia curruca Fig. 323. ly in partial postjuv moult, 2 August. MaC postjuv, partly growing. MeC postjuv and growing. GC and rest of wing juv. All GC uniformly fringed brown. Note the loose texture of the juv inner GC.
Fig. 324. ly after partial postjuv moult, 20 September. MaC postjuv. MeC postjuv. GC 1-5 juv, 6-10 postjuv. Rest of wing juv. Recognizable as ly by the distinct moult limit within GC. Juv GC brownish, postjuv GC greyish.
Fig. 327. 2y after partial prebr moult, 14 April. Outer MaC postjuv, inner MaC prebr. MeC mostly prebr. GC postjuv. Al 1 postjuv, 2-3 juv. T 7 prebr, 8â&#x20AC;&#x201D;9 postjuv or prebr. S 6 prebr. Rest of wing juv. Recognizable as 2y by the moult limit within Al and the very worn and bleached PC, P and S. This bird moulted S 6 during the prebr moult.
Fig. 325. ly after partial postjuv moult, 7 September. MaC postjuv. MeC postjuv. GC postjuv. AJ 1 postjuv, 2-3 juv. Rest of wing juv. No moult limit within GC. Recognizable as ly by the moult limit within Al.
Fig. 328. Ad after partial prebr moult, 13 April. MaC partly postbr, partly prebr. MeC postbr. T probably prebr. Rest of wing postbr. Recognizable as ad by the dark brown and less worn PC, P and S.
Fig. 326. 2y after partial prebr moult, 28 April. MaC postjuv. MeC postjuv. GC postjuv. Al 1 postjuv, 2-3 juv. T probably prebr. Rest of wing juv. Recognizable as 2y by the postjuv moult limit within Al as well as by very worn PC, P and S and pointed PC. T considerably worn, but less than the adjacent GC, thus probably prebr.
Fig. 329. Ad after partial prebr moult, 26 April. MaC mostly prebr. MeC and GC postbr. T prebr. S prebr. Rest of wing postbr. The S are considerably less worn and darker than the adjacent P and, within S, progressively less worn towards the outside. Thus, the S have probably been renewed during a long-lasting prebr moult in a descendant sequence, as found in a bird with growing S.
Sylvia communis communis
123
Sylvia communis communis Whitethroat Extent of postjuvenile moult MaC and MeC: usually all. ly with no GC moulted may retain individual juvMeC. GC: range 0-10, mean 2.5, mode 2, no GC 2.6%, all GC 1.8% (N=114). CC: one bird with all GC moulted had renewed the CC (N=86). T: none 95-3%, one (T 9) 3.5%, one bird with all GC renewed moulted all three T (N=85). In Sweden and England, a small proportion of ly moulted Al and R (Karlsson etal. 1985, Norman 1990a). In NW Russia, moult of part or all MaC, all MeC, none to nine GC, none or one Al, but not CC, T and R was observed (Rymkevich 1990). Roselaar (in Cramp 1992) mentions frequent replacement of S 6 and R 1, occasionally of some other R, for which we have no confirmation. Extent of postbreeding moult Usually whole plumage, but a small proportion of ad interrupt P-moult and a large proportion S-moult before migration. According to Rymkevich (1990), ad interrupting moult of remiges start to moult later than ad performing a complete moult. The percentage of ad with interrupted P- and S-moult varies between site and observer/year: in W Iberia, 2.7% interrupted P-moult and 2.7% S-moult (N=147; Mead & Watmough 1976). In S Spain (Goto Dofiana), 2.7% were found with interrupted P-moult and 25% with interrupted S-moult by Herrera (1974; N=37), and 40% with interrupted S-moult, but none with interrupted P-moult by Pimm (1973; N=159). A similar percentage of S-moult interruption is reported from the Netherlands (Roselaar in Cramp 1992). In Crete, 8.1% interrupted P-moult and 74.7% Smoult (N=99; Swann & Baillie 1979). On Gotland, Sweden, 75.0% interrupted S-moult (varying between years from 64% to 82%) and 7.4% P-moult (N=68; T. Fransson in lift.). Together with P and/or S also individual wing-coverts, Al and R may remain unmoulted (Fig. 336). The number of retained S may vary in the individual bird from year to year, as observed by T. Fransson (in lift.) on a bird retaining one, four and five S, respectively, in three consecutive years. P-moult may be interrupted after renewal of P 1 only (Mead & Watmough 1976, Swann & Baillie 1979), P 1-2 (Haukioja & Kalinainen 1968) or, usually, three to seven P (Dowsett 1971, Mead & Watmough 1976, own data). In NW Russia, between four and all ten P and PC are renewed (Rymkevich 1990). On Gotland, four out of five birds had retained not the outermost, but the central P (e.g. P 6, P 4—7 and P 6-7, respectively; T. Fransson in lift.). This could be interpreted as the completion of an eccentric first prebr P-moult. In this case, the postbr moult would be of complementary character to the first prebr moult, rather than the suspension of a normal descendant moult. Irregular or eccentric P-moult was also observed on the coast of the Red Sea, Sudan (G. Nikolaus in litt.). S-moult proceeds not only ascendantly from S 1, but also descendantly from S 6 (Haukioja 1971, see p. 15) or irregularly (Fig. 336). One bird from Col de Bretolet, moulted S 1+4—6 and retained S 2—3, and shows that the descendant moult wave may proceed even further than the ascendant one. S 3 and S 4 are retained most frequently (Swann & Baillie 1979, Mead & Watmough 1976, see p. 15). Four out of 68 ad on Gotland retained all S (T. Fransson in litt.). Tables presented by Swann & Baillie (1979) and Mead & Watmough (1976) and the indications in Rymkevich (1990) also suggest that this may occur occasionally elsewhere.
Fig. 330. Extent of postjuv moult on the wing and tail in ly Sylvia c. communis,
On Gotland, 35% retained at least one R (N=63; T. Fransson in litt.), Herrera (1974) and Rymkevich (1990) also report interruption of R-moult. We observed renewal of only R 1 or R 1-2 in three out of six birds with interrupted S- or P-moult on Col de Bretolet. One of these ad also retained all Al, MeC and MaC. According to Rymkevich (1990), part of the MaC, up to all MeC, up to four GC, the CC and up to two Al feathers, but never T may be retained. Stresemann & Stresemann (1968b) found that S. c. communis performs a complete moult in the breeding range, and S. c. icterops in the wintering area. Current data show that transitions between these two strategies occur frequently. In S. c. icterops, onset of P-moult was found before migration (Stresemann & Stresemann 1968b, Pearson & Backhurst 1976). 39% of the ad examined at the Red Sea coast in Sudan during August and September had no P moulted, 5% all P moulted (partly showing interrupted S-moult). The others interrupted P-moult, over 50% after renewal of P 1 or P 1—2, and some with irregular/exceptional moult patterns having some central or all outer P renewed (eccentric P-moult) (G. Nikolaus in litt.). Most of those birds showing no or only partly renewed P were probably S. c. icterops or S. c. communis/icterops intermediates (G.Nikolaus in litt.). Thus, S. c. communis, having undergone a reduced wing-feather moult in the breeding area, may show similar moult patterns during autumn migration as S. c. icterops after an extensive wing-feather moult during late summer. Other similarities between S. c. communis and icterops are found in the prebr moult (eccentric P-moult and complete moult in communis^ see below). Comments on ageing after postjuvenile and postbreeding moult Best criteria: Skull pneumatization until the end of September (p. 205). Most ly recognizable by moult limit within GC. Iris in ly dark greyish brown or greyish green, in ad yellowish. ly: 96% show a moult limit within GC (Fig. 332—334). Postjuv GC have blacker, more glossy feather centres and deeper reddish-brown fringes than juv GC. ly with no or all GC moulted are more difficult to separate from ad and are best aged on skull pneumatization or colour of iris, ly have a dark brown or greyish-brown iris (Sere 1982, Karlsson et al. 1985). As a supporting criterion, birds with uniformly light brown (unmoulted) R 6 are ly; birds with some off-white or white on R6 may be ad or ly which exceptionally renewed R 6 (Svensson 1992). Ad: All GC with black feather centres and deep reddish-brown fringes. Iris yellowish. Al on average edged more greyish-white than in ly (Fig. 335), but considerable overlap between ad and ly exists, especially in Al 1. Some ad retain unmoulted S and rarely P which are conspicuously bleached (Fig. 336).
124
Syli\via communis communts
Extent of prebreeding moult: 2y and ad Only very few birds arrive in the breeding area with a fresh prebr wing (Fig. 337). In the majority, the wing is composed of differently worn feathers without an easily interpretable pattern. From this, we assume that the majority of Whitethroats perform the prebr moult either during a very protracted period or in two temporally separated phases (see also Karlsson et al 1985). A long-lasting moult season from October until March/April was indeed observed in N Nigeria (Aidley &C Wilkinson 1987). Similarly to Motacilla flava^ Whitethroats might perform part of the moult after arrival in the wintering area, and part before leaving the winter quarters. Furthermore, differences in wear between juv, postjuv/postbr and early prebr feathers seem to be confounded by considerable individual variation in wear. Therefore, in spring, feathers are often difficult to assign to the correct feather generations. Since there are no detailed studies of moulting birds from the winter quarters, the present description of the prebr moult must be preliminary and subject to reservations. 295 spring migrants were examined in Italy, of which, depending on the feather tract concerned, 85—200 could be scored. The prebr moult is considerably more extensive than the postjuv moult. One bird underwent a complete moult. 2y moulted on average more feathers in each feather tract than ad, except in S (Fig. 331). MaC: 6% moulted all MaC shortly before spring migration, 22% had partly worn and partly fresh and 72% only worn MaC during spring migration. MeC: shortly before spring migration, 11% renewed all, 21% part and 68% no MeC. GC: all 2y renewed at least part of the GC. 16% retained some juv GC (Fig. 338), the others showed a mixture of postjuv, early and late prebr GC, often in irregular patterns. 44% of the ad renewed no GC, the others up to ten. CC: about 45%. Al: none 45% (mostly ad), one or two 11%, all 44%. T: 2y: one or two 9%> three 91%. Ad: none 15%, one or two 26%, three 59%. R: none 41%, one to five 19% (mostly R 1), six 40%. S: 2y: 43% moulted none, 55% part and 2% all S. Ad: 51% moulted none, 66% part and 15% all S (Fig. 344). Among birds with at least one S renewed, 2y birds had renewed on average 2.0 S, ad 4.3 S, usually in a descendant sequence (Fig. 331, see also p. 15), only 12% (in both
Fig. 331. Percentage of 2y Sylvia c, communis which have renewed a given S or P and of ad which have renewed a given S after completion of the prebr moult (sample size and Pmoult of ad see text).
2y and ad) having inner and outer new S separated by old ones. Ad usually renew those S that have been retained during the postbr moult (see p. 15), but occasionally, they may remain unmoulted again (Fig. 343). P and PC: 24% of 2y renewed one to seven P, mostly eccentrically (N=158; Fig. 331), one bird renewed all P (Fig. 341). Most frequently, one of the outer P (P 5, 6, 7, 8 or 9; 14 2y birds; Fig. 338), two to six outermost P (P 9-10, 8-10, 7-10, 6-10 or 5-10; eight 2y birds; Fig. 340) or two to five central P (P 8-9, 5-6, 4-8, 4-5; five 2y birds) were renewed; occasionally, P 1 or P 1-2 were renewed in addition to one to five outer P (six 2y birds; Fig. 337), rarely P 1 or P 1-2 alone (two 2y birds), and three birds had one central plus one to four outermost P renewed. Differences between left and right wings were frequent. The PC corresponding to the renewed P were not or only irregularly moulted. Among 105 ad, three birds were found having completed a suspended P-moult: one bird with P 9—10 new and two birds with P 6—10 new. This corresponds to the low percentage of suspended P-moult found after the postbr moult in Iberia (see above). In Swedish spring birds, similar moult patterns were found, differing somewhat from our findings in extent of prebr moult, notably by the absence of eccentric P-moult, but including some birds with complete P-moult (Karlsson etai 1985). The renewal of S (see Bensch et al 1991) and part of the P during winter in 2y Whitethroats is similar to the seasonally divided flight feather moult in Sylvia nisoria (Hasselquist et al 1988) and to the moult patterns of 5. cantillans (own obs., see p. 36). Comments on ageing after prebreeding moult Since the feathers are often difficult to assign to the correct feather generations, reliable ageing of spring birds on plumage characters is very difficult, even with great experience. On average, 2y have PC more abraded and bleached and of looser texture than ad (typical example in Fig. 339). PC of ad are usually slightly darker and of firmer structure than in 2y (Fig. 342). The fringe of retained juv GC (16% of 2y) may be helpful to determine some 2y (Fig. 338, GC 1—2), although it may be completely abraded (Fig. 338, GC 6). In ad, retained postbr GC usually show their fringe still in spring, but are very difficult to distinguish from prebr GC of 2y renewed during early winter. Birds with one or a few central P renewed, but outermost P old, are probably always 2y, those with a few outermost P renewed may be 2y having renewed P eccentrically up to P 10 or ad after completion of a suspended P-moult. Iris colour is reported to differ between 2y and ad in spring (Karlsson et al. 1985), but this may be partly confounded by differences between sexes (Buxton 1947, own obs.) and needs further investigation.
Fig. 332. ly after partial postjuv moult, 4 September. MaC and MeC postjuv. GC 1-7+10 juv, 8-9 postjuv. Rest of wing juv. Moult limit within GC. The renewed GC 8—9 have darker feather centres, more reddish fringes and are less worn than the juv GC.
Sylvia communis communis
Fig. 333. ly after partial postjuv moult, 12 September. MaC and MeC postjuv. GC 1—9 juv, 10 postjuv. Rest of wing juv. Recognizable as ly by the renewed GC 10 which has a deeper black feather centre and a deeper reddish-brown fringe than the juv GC.
125
Fig. 336. Ad after interrupted postbr moult, 13 September. MaC mostly postbr, some old in the undermost row. MeC postbr and old. GC postbr. CC old. Al 1 old, 2—3 postbr. S 1 +5 postbr, 2-4+6 old. T and rest of wing postbr. Easily recognizable as ad by the interrupted S-moult. The 'old' feathers are difficult to assign to feather generations. They could be juv feathers or feathers acquired during the postbr moult of the last year or, more probably (as they are not extremely worn), they could be feathers acquired during the last prebr moult.
Fig. 334. ly after partial postjuv moult, 27 August. MaC and MeC postjuv. GC 1—7 juv, 8-10 postjuv. Rest of wing juv. Distinct moult limit within GC. Renewed GC with deeper black and glossier feather centres and with more reddish fringes than juv GC.
Fig. 337. Possibly 2y after eccentric partial prebr moult, 26 April. MaC, MeC, GC, CC, Al and T renewed shortly before spring migration. S 3—6, P 1—2+5 and PC 1 prebr. Wing-coverts, Al and T are unusually fresh. The age is difficult to determine. The old PC and P are rather little worn and might suggest an ad, but the eccentrically renewed P 5 rather suggests a 2y.
Fig. 335. Ad after complete postbr moult, 9 September. Whole wing postbr. All GC fringed reddish brown. Al edged greyish-white.
Fig. 338. 2y after eccentric partial prebr moult, 3 May. MaC and MeC postjuv. GC 1—2+6 juv, rest postjuv or prebr. CC prebr. Al 1 missing, 2—3 juv. T prebr, T 7 newer than 8—9. P 6 prebr. PC and rest of wing juv. Recognizable as 2y by the retained juv GC, by the worn PC and by the single eccentrically renewed P. This bird shows a frequently observed mixture of different degrees of wear among the GC and T. A possible reading of this pattern is: GC 1-2+6 juv, GC 3-5+10 and T 8-9 and P 6 early prebr, GC 7 and T 7 late prebr, GC 8-9 postjuv like MaC and MeC.
126
Sylvia communis communis
Fig. 339. 2y after partial prebr moult, 10 May. MaC and MeC postjuv. GC 1-8 early prebr, 9-10 late prebr. CC and Al prebr. T and S 6 prebr. Rest of wing juv. Recognizable as 2y by the very worn and bleached PC. This bird probably renewed GC 1-8, CQ Al and T 8-9 during an early phase of prebr moult, GC 9—10, T 7 and S 6 during a second phase.
Fig. 342. Ad after partial prebr moult, 26 April. MaC and MeC postbr. GC 1-8 postbr, 9-10 prebr. T prebr. Rest of wing postbr. Ad after prebr moult of limited extent. Recognizable as ad by the slightly worn PC and P-tips.
Fig. 340. 2y after eccentric partial prebr moult, 4 May. MaC and MeC mainly prebr. GC mixed prebr and possibly postjuv (GC 10 missing). CC and Al prebr. T and S 6 prebr. P 6-10 and PC 8-9 prebr. Rest of wing juv. Recognizable as 2y by the very worn and bleached unmoulted PC, P and S. GC of varying degrees of wear, but no juv GC present. GC 4+9 are the freshest and have possibly been renewed together with MaC, MeC, T, S 6 and P 6-10. CC, Al and the other GC have been renewed earlier.
Fig, 343. Ad after partial prebr moult, 13 May. S 3-4 have not been moulted during both the last postbr and prebr moult. The other feathers are difficult to assign. GC 9-10, T and S 5-6 are presumably prebr, the rest of the wing postbr. Slight wear indicates an ad. This bird interrupted S-moult during the last postbr moult and did not complete S-moult during the prebr moult (S 5-6 seem to be slightly fresher than S 1-2).
Fig. 341. 2y after partial prebr moult including all P, 13 May. MaC and MeC: rwo thirds prebr, one third postjuv. GC 1—6+9—10 presumably prebr, 7—8 presumably postjuv. CC and Al prebr. T 8 prebr, T 7+9 older, probably also prebr. S 1-4 juv, 5-6 prebr. P 1-10 prebr. PC 1-2+6-9 prebr, PC 3-5 juv. Rare case of a complete P-moult. The very worn PC 3—5 suggest a 2y.
Fig. 344. Possibly ad after partial prebr moult including all S, 13 May. S 1—6, T and GC 10 prebr. Rest of wing presumably postbr. Example of a prebr moult including all S. PC firmly textured and only slightly worn and bleached, suggesting an ad.
Sylvia borin
127
Sylvia borin Garden Warbler Extent of postjuvenile moult MaC and MeC: according to observations on actively moulting birds, MaC and MeC are renewed at least partially (Rymkevich 1990, M. Widmer in litt.). Since moult limits within MaC and MeC are only rarely recognizable, the extent of postjuv moult within MaC and MeC remains unclear. GC: range 0-4, mean 1.9, mode 2, no GC 7.3% (N=809). The extent of postjuv moult decreases slightly as the autumn migratory season proceeds (Fig. 346). According to Rymkevich (1990), the postjuv moult includes one to three GC, all MeC and none to all MaC, but never Al, CC, T, S and R. Surprisingly, Ginn & Melville (1983) mention that ly usually renew six or more GC and even inner S. Also Norman (1990a) indicates renewal of outer GC and T (cf. Roselaar in Cramp 1992). We never observed renewal of outer GC and only exceptionally replacement of probably accidentally lost single T (five birds). Extent of postbreeding moult The postbr moult is very variable in extent: it may be almost completely suppressed, but usually involves part of the body-feathers, in 27% of birds T and GC, rarely S (3%) or P (4%) and, exceptionally, it may be complete. Body-feathers, MaC and MeC: body-feathers and MaC are usually only partly moulted, the MeC partly, completely or not at all. GC: range 0-8, often in irregular sequence, mean 0.7, mode 0, no GC 73.4%(N=128). T: none 76.5%, one 15.8%, two 4.3%, three 3.4% (N-234) (see p. 15). Asymmetries between left and right wing are frequent. CC:5%(N=128). R: none 78.3%, one 10.8%, two 5.0%, three to six 5.8% (N=120) (see p. 16). Asymmetries are frequent. S: 3% (N=183) renewed one to three S: two birds S 1, one bird S 6, another S 5-6 and another S 4-6. P and PC: 4% (N=183) started a regular P-moult including the corresponding PC (no S renewed): two birds showed interrupted P-moult (P 1 or P 1-2 and the corresponding PC renewed), five birds had growing P and corresponding PC (one bird P 1, three birds P 1-2, one
Fig. 346. Extent of GCmoult during autumn in ly Sylvia borin after completion of the postjuv moult (data grouped in five-day periods; the first bar includes the period 30 July-8 August, the last 3-22 October). White = none or one GC moulted, wide hatching = two GC moulted, narrow hatching = three or four GC moulted.
Fig. 345. Extent of postjuv moult on the wing and tail in ly Sylvia borin.
bird P 1-4 new or growing), thus P-moult might have proceeded further. Three additional birds had only PC 1 renewed (on one wing only). One bird from 25 August, ringed at the same place in Switzerland as ly the year before, had a particular P-moult pattern on both wings: P 1 renewed, P 2-7 old, P 8-9 finishing growing (S not recorded; H. Leuzinger in litt., documented by photos). This is a rare case of an ad passerine with eccentric P-moult. Another indication of eccentric P-moult is given by an ad with P 6 renewed on one wing only together with S 6. Complete moult was found in an ad ? (dissected) from 18 August which renewed the entire plumage. Thus, in ad Garden Warblers, P-moult may be interrupted after a regular descendant or an eccentric beginning, or it may be complete. Two birds from England and two from Spain have been observed shortly before finishing wing-feather moult, and thus were probably performing a complete moult (Gladwin 1969). Considerably more records of birds starting or interrupting P-moult are available: 14 birds from Belgium had one to four innermost P renewed or growing, one of them P 1-9 on the left wing and P 1-6 on the right wing (Dehaen & Herroelen 1971, Herroelen 1982b, 1988). Two birds from France had P 1 growing (Olioso 1987). One out of 400 ad from NW Russia replaced six P, two S, all T and had growing R (Rymkevich 1990). Among 74 birds from Spain, two had interrupted P-moult after renewal of P 1 and one after renewal of P 1â&#x20AC;&#x201D;4 (Mead & Watmough 1976). The most detailed account is provided by Herrera (1974) from Spain. Compared to Switzerland (4% with new P and 24% with new
Fig. 347. Extent of postbr moult on the wing and tail in ad Sylvia borin.
128
Sylvia borin
T), a considerably higher percentage of 21% (N=114) was found to interrupt P-moult after renewal of one to five innermost P (four of these birds also had S 1 renewed) and of 66% with one to three renewed T; at least seven birds had all R renewed, and many others part of the R which was interpreted as replacement of accidentally lost feathers. Indications of the onset of P-moult are given without details for Germany (Kasparek 1981) and Sweden (Svensson 1992). From these reports, it may be inferred that populations of southern, southern central and W Europe may be more likely to start P-moult in the breeding area than birds of northern origin (Gladwin 1969, Herrera 1974, ownobs.). Comments on ageing after postjuvenile and postbreeding moult Best criteria: Skull pneumatization until the end of September (p. 205). Difference in wear of GC and T. ly: Whole plumage, especially fringes of all T and GC, fresh and intact. Fringes of GC and T slightly broader than in ad and brownish or greenish-brown. 93% show a moult limit within GC (Fig. 349) which is distinctly less conspicuous than in those ad with renewed GC. Postjuv GC are of firmer structure and have more greenish-grey and glossier feather centres than juv GC. Ad: Although wear is not as pronounced as in other warblers, ad are easily recognized by the generally more bleached and worn plumage (Fig. 350). Especially the fringes of T and inner GC are, if not moulted, worn and abraded, rendering the fringe narrower than in ly and greyish. Renewed GC contrast more with the adjacent old GC than in ly (Fig. 351). Birds with renewed T, P, PC and S (Fig. 351 and 352) are ad. The very few ad performing a complete moult may be missed if skull pneumatization is not checked. Extent of prebreeding moult Usually whole plumage. Only 11 birds (1.5%) out of 715 spring migrants examined in Italy showed one to six S older than the P (usually S 6 [Fig, 353], more rarely S 5, in single birds S 4-5, S 4-6, S 4+6, S 3+6, S 1â&#x20AC;&#x201D;6, respectively; often asymmetric between the wings). Rarely, some R and T may look older than the rest of the remiges. It remains uncertain whether these older feathers have been renewed during the postbr moult but not during the prebr moult or whether the prebr moult was incomplete and these feathers date back to the last prebr moult. Although postbr P-moult interruption occurs regularly in a small percentage of ad, no spring bird with inner P older than outer P was found, which would indicate a resumption of a suspended P-moult. Therefore, P renewed during the postbr moult are probably renewed again during the following prebr moult, approaching two complete moults annually in these few birds. An indication of this is provided by caged birds which exceptionally renew the flight feathers twice annually (Bairlein in Glutz & Bauer 1991). Comments on ageing after prebreeding moult: 2y and ad According to our experience, 2y and ad cannot be separated on plumage characters.
Fig. 348. ly after partial postjuv moult, 4 August. MaC and MeC probably postjuv, GC and rest of wing juv. Recognizable as ly by the fresh plumage, especially the intact fringes of all T and GC. This bird shows no moult limit within GC.
Fig. 349. ly after partial postjuv moult, 14 August. MaC and MeC probably postjuv. GC 1-7 juv, 8-10 postjuv. Rest of wing juv. Recognizable as ly by the fresh plumage and the inconspicuous moult limit within GC. Postjuv GC 7-10 slightly firmer textured and more greenish-grey than juv GC.
Fig. 350. Ad after partial postbr moult, 24 August. Whole wing prebr. This Bird renewed no coverts or remiges during the postbr moult. Recognizable as ad by the worn plumage, especially GC andT.
Sylvia horin
Fig. 351. Ad after partial postbr moult, 17 August. MaC and MeC prebr. GC 8 postbr, rest prebr. T 7 prebr, 8-9 postbr. PC 1 postbr. Rest of wing prebr. Recognizable as ad by the worn plumage, especially GC, and the renewed T. Renewed GC contrast much more with the old GC than in ly (cf. Fig. 349).
Fig. 352. Ad after partial postbr moult interrupted within P, 10 August. MaC prebr. MeC 1-5 prebr, 6-8 postbr. GC 1+9-10 prebr, 2-8 postbr. T 7-8 prebr, 9 postbr. P 1-2 and PC 1-2 postbr. Rest of wing prebr. Renewed T and P-moult interruption are typical of a few ad.
Fig. 353. 2y/ad after complete prebr moult, 15 May. S 6 was not moulted during the prebr moult. Ageing spring birds on plumage is not possible.
129
130
Sylvia atricapilla
Sylvia atricapilla Blackcap Extent of postjuvenile moult
MaC and MeC: all.
GC: range 3-10, mean 9.0, mode 10, all GC 47.0% (N=1014). CC: 12.2% (N=705). Al: none 60.0%, one 30.5%, two 8.6%, three 0.8%(N=708). T: none 19.9%, one 11.3%, two 41.9%, three 26.8% (N-682) (see p.
33). R: none 96.9%, one 1.0% (usually R 1), two to six 2.0% (N=818) (see
p. 34). S, P and PC: five birds (1.0%) were found with renewed S 6 on both wings. Another bird had PC 1-4 renewed and PC 5-6 growing on both wings, but all P old. Another bird had PC 1 growing on one wing only. Among 68 2y examined in Italy during spring migration, two were found with eccentrically renewed P: one had P 7 and S 4-6 renewed on both wings, the other P 7-9 and S 6 on both wings; in both birds, all GC, CC, Al 1-2, all T and all R were moulted, but not the PC. Judging by the degree of wear, all these feathers had been renewed during the postjuv moult and not during winter or spring. The extent of postjuv moult is correlated among GC, CC, Al, T and R. T may be renewed when at least four GC are moulted, Al when at least five GC, and R and CC when at least eight GC moulted (Fig. 355). The postjuv moult is significantly more extensive in S than in $: S moulted on average 9.2 GC, 1.8 T, 15% the CC and 44.1% one to three Al; 9 moulted on average 8.8 GC, 1.6 T, 8.6% the CC and
Fig. 355. Relationships between the number of postjuv GC and the percentage of individuals with renewed CC, Al, T and Rin ly/2y Sylvia atricapilla which have completed their postjuv moult.
Fig. 354. Extent of postjuv moult on the wing and tail in ly/2y Sylvia atricapilla.
35.2% one to three Al. In both sexes, the extent of postjuv moult decreases as the autumn migratory season proceeds (Fig. 356). In spring, the extent of postjuv moult is higher than in autumn in S (mean number of GC moulted in spring 9.4, in autumn 9.0) and in 9 (means 9.2 and 8.7), without significant seasonal trend and no significant difference between birds from Italy and S Switzerland (Fig. 356). During autumn migration in Belgium (Herremans 1991), 51.2% of the <J (N=2575) and 44.8% of the 2 (N=1592) had renewed all GC, which is similar to the value found over a longer autumnal period in Switzerland for 6 (50.6%), but higher than that for ? (38.1%). In Belgium, significant differences between the sexes and a decrease during September in the number of renewed GC were also found, along with differences between a coastal and an inland site (Herremans 1991). In NW Russia, Rymkevich (1990) found part or all MaC, all MeC, four to ten GC, none to three Al and sometimes CC, but never R and T renewed.
Extent of postbreeding moult Whole plumage. Rarely, ad may temporarily suspend P-moult in summer after renewal of P 1 or P 1â&#x20AC;&#x201D;2 (four birds). Exceptionally, S 6 may be retained (Fig. 366). Comments on ageing Best criteria: Skull pneumatization until the end of September (p. 205). Moult limits within GC, T, Al and between T and S usually diagnostic of ly/2y, although sometimes difficult to recognize.
Fig. 356. Mean number of postjuv GC during autumn (Switzerland, data grouped in five-day periods; the first value includes the period 4-28 August, the last 18-31 October) and spring (CH = southern Switzerland; I = Ventotene Island, Italy) of 6 (dots) and 9 (triangles) 1 y/2y Sylvia atricapilla which have completed the postjuv moult.
ly/2y: 53% of ly/2y show a moult limit within GC, which is easily recognized. The renewed GC are tinged greenish-grey, at least at the fringe, juv GC are tinged brownish (Fig. 358 and 359). ly/2y with all GC renewed are more difficult to age. They can be recognized by moult limits within T (Fig. 360 and 362), between T and S (Fig. 363) and within Al and CC (Fig. 360 and 361). Renewed Al 1 and CC are usually similar in colour to the adjacent postjuv MaC, juv Al 1 and CC are browner (cf. Fig. 359 with 361); however, the differences are not always clear. Moult limits within T are more easily recognizable. Birds with all T renewed (27%) show a slight difference in colour between the outer fringes of postjuv T and juv S (Fig. 363) which is best detected when the wing is half-closed. Rarely, moult limits within S and P occur. Ageing birds without a moult limit within GC is sometimes difficult and, before October, should be supported by skull pneumatization or iris colour (Leverton 1987). The shape of R, suggested as an ageing criterion (Spencer & Mead 1979, Svensson 1992), is highly variable
Sylvia atricaptlla
and shows a large overlap between the age classes. The same applies to the shape of PC (Svensson 1992). ly cT in summer/autumn often have brownish fringed feathers of the crown. $ with all black crowns may be 1 y or ad. According to our experience, the same plumage criteria as in autumn can be used in spring. There is only a little extra wear and moult limits are still recognizable. Until now, we have no indication that the prebr moult affects feathers of the wing.
131
Fig. 359. ly 9 after partial postjuv moult, 13 October. MaC and MeC postjuv. GC 1 juv, 2-10 postjuv. T 7+9 juv, 8 postjuv. Rest of wing juv. Recognizable as ly by the brownish juv GC 1.
Ad: Whole wing without moult limit within GC, T, Al and between T and S. Ad cT usually have no brownish fringes on the black crown, which may be used as a supporting criterion. Iris colour more reddishbrown than in ly which have a grey-brown iris until early October (Leverton 1987). Extent of prebreeding moult Several authors observed a partial prebr moult, including not only body-feathers, but also T and GC fWitherby et al. 1943, Williamson 1968, Ginn & Melville 1983, Roselaar in Cramp 1992, Svensson 1992). However, in over 250 birds examined in spring we could find no indications of wing-coverts or T renewed during winter or spring. According to Berthold & Schlenker (in Glutz & Bauer 1991), the prebr moult may comprise only part of the small feathers and probably does not occur in the majority wintering in the northern wintering area. Also according to Stresemann (1920), the prebr moult may be completely suppressed. However, all birds wintering in Kenya and Uganda renew body-feathers and most of the wing-coverts (Pearson 1978, Roselaar in Cramp 1992). Probably, the prebr moult is dependent on population or wintering area.
Fig. 357. ly in juv plumage, 1 August. Whole wing juv. MaC, MeC and GC loosely textured, typical of juv plumage. All GC tinged brownish.
Fig. 358. 2y <J after partial postjuv moult, 23 April. MaC and MeC postjuv. GC 1—4 juv, 5—10 postjuv. Rest of wing juv. Distinct moult limit within GC. Juv GC 1—4 brownish, postjuv GC 5-10 greenishgrey.
Fig. 360. ly c? after partial postjuv moult, 5 October. MaC, MeC and GC postjuv. Al 1 postjuv, 2—3 juv. T 7 juv, 8—9 postjuv. Rest of wing juv. Recognizable as ly by the moult limits within T and Al. Postjuv Al 1 of the same colour as the adjacent MaC and MeC. Juv CC edged brownish as the PC.
Fig. 361. ly 6 after partial postjuv moult, 19 September. MaC, MeC and GC postjuv. CC postjuv. Al 1 postjuv, 2—3 juv. T 8—9 postjuv, 7 juv. Rest of wing juv. Postjuv CC and Al 1 fringed greenish-grey like the adjacent MaC and MeC. Such birds are often difficult to distinguish from ad.
132
Sylvia atricapiLla
Fig. 362. 2y (5 after partial postjuv moult, 12 April. MaC, MeC and GC postjuv. T 8â&#x20AC;&#x201D;9 postjuv, 7 juv. Rest of wing juv. Recognizable as 2y by the moult limit within T and the brownish fringed Al 1 and CC. Renewed T 8-9 greenish-grey like the GC, juv T 7 brownish like S.
Fig. 363. 2y cT after partial postjuv moult, 8 April. MaC, MeC, GC and T postjuv. Rest of wing juv. The difference in colour between the postjuv T 7 and the juv S 6, diagnostic of 2y, is only slight and difficult to detect. The outer web of T 7 is slightly greyer than that of S 6.
Fig. 364. Ad <3 after complete postbr moult, 15 September. Whole wing postbr. Fringes of all PC, GC, CC and Al similarly coloured.
Fig. 365. Ad <3 after complete postbr moult, 7 April. Whole wing postbr. No moult limits detectable. Wear until spring is generally only slight.
Fig. 366. Ad 2 after postbr moult arrested at S 6, 22 September. Exceptionally, S 6 has not been renewed and is bleached. The rest of the wing is fresh and shows no moult limits.
Phylloscopus collybita
133
Phylloscopus collybita Chiffchaff Extent of postjuvenile moult MaC and MeC: usually all. ly with few or no GC moulted may retain some juv MaC and/or MeC. GC: range 0-10, mean 5,4, mode 6, no GC 4.0%, all GC 6.0% (N=430). CC: 48.9%. Al: none 63.3%, one 35.5%, two 1.2% (N=4l 1). T: none 43.6%, one 12.7%, two 13.1%, three 30.7% (N=4l 1) (see p. 33). R: none 54.5%, one 38.2% (usually R 1), two 5.6%, three 1.2%, six 0.5%(N=4ll)(seep. 34). S: 8.5% renewed S 6 (when at least seven new GC), of which two birds renewed also S 5 on one wing only (N=272). The extent of postjuv moult is correlated among GC, CC, Al, T and R (Fig. 368). The extent of postjuv moult decreases significantly as the autumn migratory season proceeds (Fig. 369). In England, the postjuv moult may also comprise all GC, T and part of the Al, R and rarely one or two S (Norman 199la). GC- and Rmoult seems to be more extensive than in birds examined in Switzerland, but the data are not directly comparable because they are based on actively moulting birds. In NW Russia, 5-8% renew T 7-8 and R 1, while CC and Al are apparently retained (Rymkevich 1990). Fennoscandian birds are reported to moult only a few GC (often only two) and MeC and some or all T, but some may moult more extensively (Svensson 1992). Roselaar (in Cramp 1992) reports that up to three innermost S may be renewed.
Fig. 368. Relationships between the number of postjuv GC and the percentage of individuals with renewed CC, Al, T and Rin ly Phylloscopus collybita which have completed their postjuv moult.
Fig. 367. Extent of postjuv moult on the wing and tail in ly Phylloscopus collybita.
Extent of postbreeding moult Whole plumage. One ad from 23 October retained Al 2 and some MaC on both wings. In NW Russia, occasionally individual Al and wing-coverts are retained and in two $ from the second half of September, S 3—6 and S 5—6, respectively (Rymkevich 1990). Comments on ageing after postjuvenile and postbreeding moult Best criteria: Skull pneumatization until mid-September (p. 205). Moult limits within GC, T, S and R and between T and S diagnostic of ly, but sometimes difficult to detect. ly: 90% of ly show a moult limit within GC, which is often difficult to detect when among the inner GC (Fig. 373). Moult limits among central GC are generally easier to see, but due to variable coloration of juv GC may be more (Fig. 375) or less (Fig. 374) conspicuous. Juv GC are slightly lighter with a brownish tinge and the fringes are less green than in postjuv GC. Postjuv GC, and also postjuv T and R, have darker and greyer feather centres which are usually more glossy than juv feathers, ly with all GC moulted usually have one or several T and R 1 renewed, thus can be recognized by moult limits within R and T or between T and S, which are easy to detect. A few birds moult S 6, and thus show a moult limit within S (Fig. 376). Some ly without renewed GC are recognizable by moult limits within MaC and MeC (Fig. 372). Many ly show some juv body-feathers up to October which are very loosely textured. Ageing according to general shape and wear of R (Spencer & Mead 1979) is not recommended. Ad: Whole plumage fresh and not worn. No moult limits within MaC, MeC, GC, T, S and R, centres of these feathers often slightly glossy. Fringes of GC, T, S, P, PC, Al and CC dark green or brownish-green, not yellowish-green. PC usually more firmly textured than in ly (Fig. 377). Extent of prebreeding moult: 2y and ad
Fig. 369. Mean number of postjuv GC during autumn of ly Phylloscopus collybita which have completed the postjuv moult (data grouped in five-day periods; the first value includes the period 14 August—12 September).
MaC and MeC: MaC and MeC are probably renewed only rarely and if so only the proximal ones. GC: range 0-6, mean 0.1, mode 0, no GC 95.8% (N=262). GC are often moulted in irregular sequence. T: none 59.9%, one 15.6% (mostly T 8), two 13.7% (mostly T 7-8), three 10.7% (N=262) (seep. 15). R: none 81.3%. one 16.8% (R 1), two 1.5% (mostly R 1-2), three 0.4%(N=262)(seep. 16). S: two birds renewed S 6 in addition to T 7-9 and T 7-8, respectively (N=262).
134
Phylloscopus collybita Fig. 373. ly after partial postjuv moult, 27 September. MaC and MeC postjuv. GC 1-7 juv, 8—10 postjuv. Rest of wing juv. The feather centres of the juv GC are slightly lighter, browner and more worn than those of the postjuv GC. Postjuv GC are more glossy and have slightly more intensive green fringes than juv GC.
Fig. 370. Extent of prebr moult on the wing and tail in ad and 2y Phylloscopus collybita. Comments on ageing after prebreeding moult Ageing spring birds is often difficult and some are impossible to age. Although often difficult to see (Fig. 378), the moult limits within GC due to the postjuv moult may be still recognizable in spring (Fig. 379). Postjuv moult limits within T and R are blurred by feather wear. Distinct moult limits within T and R (Fig. 378 and 380) are always due to the prebr moult and irrelevant for ageing. Juv remiges and coverts are more intensively worn in spring than the corresponding postbr feathers of ad. Thus, birds without visible moult limits due to the postjuv moult which have their remiges and GC worn only a little are ad (Fig. 381), those with very worn remiges and GC are 2y (Fig. 380). Intermediates must be left undetermined.
Fig. 374. ly after partial postjuv moult, 2 November. MaC and MeC postjuv, except one juv MaC. GC 1—5 juv, 6-10 postjuv. Rest of wing juv. Recognizable as lyby the moult limit within GC. The juv GC show lighter feather centres, lighter and more greyish-green fringes and are already more worn than the postjuv GC.
Fig. 371* ly in juv plumage, 31 July. Whole wing juv. Especially MaC and MeC conspicuously loosely textured, typical of juv feathers. Fig. 372. ly after partial postjuv moult, 30 October. MaC postjuv, some distal ones juv. MeC postjuv, outermost juv. GC and rest of wing juv. Recognizable as ly by the retained juv MaC and MeC, which are more loosely textured, tinged greyish and lighter than postjuv MaC and MeC.
Fig. 375. ly after partial postjuv moult, 13 October. MaC and MeC postjuv. GC 1—4 juv, 5—10 postjuv. T 8 postjuv. Rest of wing juv. Distinct moult limit within GC. The four juv GC have less glossy feather centres and more yellowish fringes than the postjuv GC, The fringe of the renewed T 8 is more deeply green than in the juv T 7 and 9.
Phylloscopus collybita
Fig. 376. ly after partial postjuv moult, 30 September. MaC and MeC postjuv. GC postjuv. CC and Al 1 postjuv. T 7-9 and S 6 postjuv. Rest of wing juv. Recognizable as ly by the moult limit within S. The renewed S 6 and T 7-9 have darker, glossy feather centres and more deeply green fringes than the juvS 2-5.
135
Fig. 379, 2y after partial prebr moult, 19 April. Inner MaC and MeC probably prebr, outer ones postjuv. GC 1-4 juv, 5-10 postjuv. T juv or postjuv. Rest of wing juv. The moult limit due to the postjuv moult is still easily recognizable. The juv GC are lighter, more greyish-green and more worn than the postjuv GC.
Fig. 377. Ad after complete postbr moult, 13 October. Whole wing postbr. No moult limits within GC, T, and between T and S. Remiges fringed more deeply green and PC less loosely structured than in ly.
Fig. 380. 2y after partial prebr moult, 17 April. MaC and MeC postjuv. GC 1-6 juv, 7-8 prebr, 9-10 postjuv. T 7-9 prebr. Rest of wing juv. The moult limit due to the postjuv moult has vanished because of the intervening prebr GC 7-8. However, GC 1-6 are heavily worn and, therefore, very probably juv.
Fig. 378. 2y after partial prebr moult, 20 April. MaC and MeC postjuv. GC 1-4 juv, 5-10 postjuv. T 7-8 prebr, 9 postjuv or juv. S 6 prebr. Rest of wing juv. The moult limit within GC due to the postjuv moult is difficult to detect. The first four juv GC are slightly browner than the postjuv GC.
Fig. 381. Ad after partial prebr moult, 16 April. T 8 prebr. Rest of wing postbr (MaC and MeC difficult to assign). The whole wing is less worn than in 2y. PC more firmly textured and less worn than in 2y.
136
Phylloscopus trochilus
Phylloscopus trochilus Willow Warbler Extent of postjuvenile moult MaC and MeC: In freshly moulted birds, juv and postjuv MaC and MeC are difficult to distinguish. The differences between the feather generations become evident only as the feathers wear. Thus, the following data are preliminary. 52% replace no or very few MaC, 39.5% up to three quarters and only 8.5% renew all MaC (N=130). 65.5% moult no MeC, the rest one to eight, mostly three or four MeC (N=145). GC: range 0-6, mean 0.4, mode 0, none 83.0% (N=347). T and R: four birds renewed T 7, 8 or 9 on one wing, three birds R 1 on one side and one bird T 7+9 on one, T 8 and R 4 on the other side (N=343). Probably not all renewed T and R can be attributed to accidental loss. There is no seasonal trend in the extent of postjuv moult. In England, the examination of actively moulting birds suggests that all MaC are moulted, all MeC in some birds, only inner MeC in most, and one or two inner GC in a few birds (Norman 1981). In NW Russia, MaC and MeC are only partly renewed in many birds and GC seem not to be moulted; migration may start before completion of postjuv moult (Rymkevich 1990). Extent of postbreeding moult Usually whole plumage. In Switzerland, 3.8% were found to retain one to four S (mostly S 3-6 or S 4-5, Fig. 387, see p. 15) and 4.4% retained one to a few MaC, one bird Al 1 and CC (N=l 58). In Iberia, 2.4% of ad migrants showed interrupted S-mouIt (N=250, Mead & Watmough 1976). In Crete, 8.9% of all birds caught (ad and ly) retained S (N=450, Swann & Baillie 1979). In NW Russia, on average 8.3% interrupted S-moult, varying between 1—21% between years and being more frequent in 9 than in S. Usually S 5 and/or 6 were retained, occasionally some MaC and rarely S 2—6 (Rymkevich 1990). In migrants, interruption of P-moult has not been reported so far. However, Rymkevich (1990) observed retention of P 10. P-moult interruption in a bird from 10 July in Belgium after renewal of P 1—3 (Herroelen & van der Meiren 1966) is probably attributable to breeding and not to migration. Indeed, moult suspension of late breeding birds has been described by Norman (1990b).
Fig, 382, Extent of postjuv moult on the wing and tail in ly Phylloscopus trochilus.
Extent of prebreeding moult: 2y and ad Whole plumage. The Willow Warbler is one of the very few palearctic passerine species in which ad perform a complete moult twice a year (see p. 22). An extensive review comparing postbr and prebr moult is provided by Underhill et al. (1992). A single case of apparently completely suppressed prebr moult is reported by Andre & Fouarge (1967). Other authors (Drost 1939, Busse 1984, Ginn & Melville 1983, Svensson 1992) consider the possibility that not all 2y perform a complete prebr moult, but do not suggest why this should concern 2y only. Among 937 spring migrants examined in Italy and Switzerland between March and May, we found no indication of incomplete or suppressed prebr moult. Although some of these migrants showed rather worn T and GC (Fig. 388), P and S were never so worn to suggest incomplete prebr moult. However, about 2% had all or some inner S, occasionally also innermost GC and T 7, distinctly fresher than P. This indicates a prolonged moult period or even temporarily suspended moult in the winter quarters. Fig. 383. ly after partial postjuv moult, 15 August. Whole wing juv. No wing-coverts have been renewed.
Comments on ageing after postjuvenile and postbreeding moult Best criteria: Colour of underparts diagnostic in most birds, but ageing requires some experience. Skull pneumatization useful only until the beginning of August (p. 205), but many ly show incomplete pneumatization until September. ly: Only 17% show a moult limit within GC and 34.5% a moult limit within MeC (Fig. 384 and 385). These limits, especially in the MeC, are not easy to detect. Therefore, always check colour of underparts. Throat and breast and, depending on the subspecies, also belly are uniformly yellow. Whole undertail-coverts uniformly light yellow, not only their fringes. Northern birds generally have less yellow on belly and breast and may be difficult to separate from ad. Ad: Throat and breast generally white or slightly streaked yellow or buffish, belly mostly without yellow tinge. Undertail-coverts white, faintly fringed light yellowish. As ad start migration just after finishing moult, some migrants may still show sheaths at the base of innermost S. Also check for retained S and MaC (Fig. 386 and 387).
Fig. 384. ly after partial postjuv moult, 15 August. MaC partly juv, partly postjuv. MeC 1—4 juv, 5—8 postjuv. GC 1-8 juv, 9-10 postjuv. Rest of wing juv. Renewed MeC with
greenish, juv MeC with greyish barbs. Postjuv GC 9—10 have more blackish and slightly glossy feather centres and greener fringes than juv GC.
Phylloscopus trochilus Fig. 385. ly after partial postjuv moult, 20 August. MaC juv, except proximal postjuv. MeC 1-3 juv, 4-6 postjuv, 7 probably juv. GC 1-6 juv, 7-10 postjuv. T 7 postjuv, 8-9 juv. Rest of wing juv, Exceptionally extensive postjuv moult. Renewed MeC and GC with green fringes and darker feather centres, juv MeC and GC with greyish fringes fading into the greyish feather centres. T 7 is replaced on one wing only.
Fig. 386. Ad after complete postbr moult, 24 August. With the exception of three distal MaC in the undermost row, whole wing postbr. Recognizable as ad by the retained and very worn MaC.
Fig. 387. Ad after interrupted postbr moult, 11 September. Two MaC in the undermost row and S 4â&#x20AC;&#x201D;5 have been retained, rest of wing postbr. Retained prebr S 4-5 distinctly more bleached than adjacent S, indicating ad.
137
Fig. 388. 2y/ad after complete prebr moult, 3 May. Whole wing prebr. Example of a wing showing already advanced abrasion on MaC, MeC, GC and T. Ageing not possible.
Fig. 389. 2y/ad after complete prebr moult, 18 April. Whole wing prebr. Example of a wing showing only slight abrasion. Ageing not possible.
138
Muscicapa stria ta
Muscicapa striata Spotted Flycatcher Extent of postjuvenile moult Body-feathers: only 24% of ly moult all, 76% retain some juv bodyfeathers, especially on rump and shoulders (N=269). MaC: usually all. MeC: usually all, occasionally, individual juv MeC may be retained. GC: range 0-3, mean 0.6, mode 0, no GC 57.2% (N=313). The extent of postjuv moult decreases as the autumn migratory season proceeds (Fig. 391). The postjuv moult Is of very limited extent, as also observed in NW Russia where usually all body-feathers, but occasionally only half of them, part or all MaC and MeC and none to two GC are moulted (Rymkevich 1990). Occasional replacement of T or S 6, as claimed by Ginn & Melville (1983), could not be confirmed by our data and may refer to ad. Extent of postbreeding moult MaC: usually partly renewed, rarely all or none. MeC: usually not renewed, rarely part or all. GC: 27.8% renewed one or two GC, mostly in irregular sequence. GC 7, 8, 9 and 10 are renewed most frequently. One ad renewed six GC (N=72). T: none 13.5%, one 33.7%, two 28.1%, three 24.7% (N=89) (see p. 15). R: 9.8% of ad renewed one or two R, often in irregular sequence (N-51). S: 13.4% (11 out of 82 ad) renewed one to three S: five birds S 2-3, three birds S 3, one bird S 2—4 and two birds S 6 (see p. 15). Asymmetries between left and right wing were frequent. P: P-moult was not recorded by us. Rymkevich (1990) reports that on average only about half of the bodyfeathers, less than half of the wing-coverts and in one ad R 1 are renewed in NW Russia. Furthermore, more than 50% renew T 8, less than 50% T 7+9, T 7+8 or T 7. In Finland, 77% of ad moult on average 1.8 T, most frequently T 8 (N=178; Hyytia & Vikberg 1973, see also Haukioja & Kalinainen 1972), and among 119 a4 migrants on Crete, 87% moulted on average 1.8 T (Swann & Baillie 1979), which is similar to our data from Switzerland, where 87% of ad renewed on average 1.9 T. Also in Great Britain, most ad are reported to moult some T (Ginn & Melville 1983).
Fig. 391. Extent of GCmoult during autumn in ly Muscicapa striata after completion of the postjuv moult (data grouped in five-day periods; the first bar includes the period 4-13 August, the last 28 September-17 October). White = no GC moulted, wide harching = one GC moulted, narrow hatching = two or three GC moulted.
Fig. 390. Extent of postjuv moult on the wing and tail in ly Muscicapa striata.
Renewal of one to three S was recorded on one out of 178 ad in Finland (Hyytia & Vikberg 1973), on three ad (2.5%, N=119) on Crete (Swann & Baillie 1979), on 11 ad in Great Britain (Ginn & Melville 1983), on five ad (15-6%, N=32) in Iberia (Mead & Watmough 1976) and on two birds in NW Russia (Rymkevich 1990). Among the birds from Iberia, three ad had S 6, one S 2—3 and one S 4 renewed, the two Russian birds S 2+6 each. Onset of P-moult in Europe is apparently very rare. Mead & Watmough (1976) mention one ad from Spain with P 10—9 renewed and P 8 growing, and Clarabuch (1992) one ad with P 10-9, S 6, T 7-9 and R 2—6 renewed, P 8—7, S 5 and R 1 almost full-grown. The information regarding one ad which started to moult P descendantly in Great Britain (P 1-2 growing, 3-10 old; Ginn & Melville 1983) should be reconsidered. In autumn, after the postbr moult, two types of moult interruption have to be clearly distinguished: (1) interrupted postbr moult and (2) interrupted prebr moult. In the first case, some fresh, dark feathers, acquired during the postbr moult, are interspersed among the old prebr feathers (Fig. 395 and 396), mostly T, GC and S. In the second case, some very worn and bleached feathers (mostly S and PC), not moulted during the prebr moult (thus at least one year old), are present among the old prebr feathers (see extent of prebr moult). Comments on ageing after postjuvenile and postbreeding moult Best criteria: Distinct difference in wear, especially on wing-coverts. Light tips on inner GC diagnostic of ly. Skull pneumatization until the beginning of September (p. 205). ly: Plumage hardly worn, GC with distinct light tips. 57% of ly renew no GC, and show light tips on all GC (Fig. 393). ly with a moult limit within GC (Fig. 394) can easily be distinguished from ad with renewed GC by the light tips on the retained juv GC. 76% of ly retain some juv body-feathers, especially on rump and shoulders, which are recognizable by prominent light tips (Fig. 393). Ad: Plumage worn, GC with narrow light fringes, but without light tips. Postbr GC are conspicuous by their dark colour (Fig. 396). 87% of ad renew one to three T (Fig. 395)) which does not occur in ly according to our observations. Sequence and extent of prebreeding moult: 2y and ad Sequence: The Spotted Flycatcher has a unique sequence of wing feather moult, not found in any other passerine (Williamson 1960, 1972, Diesselhorst 1961, Stresemann 1963b): P are moulted ascendantly, but P 10 usually only shortly before or after shedding P 7. The PC are nor moulted together with the corresponding P (Williamson
Muscicapa striata
Fig. 392. Extent of postbr moult on the wing and tail in ad Muscicapa striata.
1972), but probably before or at the beginning of P-moult. Two birds in P-moult, examined by us in the Vienna Museum, showed PC already renewed (P 9-7 and P 4—1 growing, respectively). T-moult starts at about the same time as P-moult (Stresemann 1963b, Williamson 1972). After the renewal of the T, S-moult starts with S 6 (according to Williamson also with S I ) and may be temporarily halted after the renewal of S 6 (Stresemann 1963b). Two birds (Vienna Museum), however, show that S-moult may start before the renewal of the T (S 6 growing, T 7-9 and S 1-5 old; S 6 and T 8 new, T 7+9 and S 5 growing, S 4—1 old, respectively), which is also mentioned by Diesselhorst (1961). S-moult proceeds convergently from S 6 and S 1 towards the centre. S 2 and 3 (S 3 and 4 according to Williamson 1972) are moulted last when all P and often all other S are full-grown. The R are moulted centripetally from outside to inside. The Al is renewed early during the renewal of P 10—7, The prebr moult can be protracted and moulting birds can be found between November and March (Stresemann 1963b). Extent: usually whole plumage. According to our observations on 145 spring migrants in Italy, MaC, MeC, CC, Al, R and P were always moulted. S: 10.3% retained one to three central S: eight birds S 2-3, four birds S 3 and one bird S 2+4, S 3-5 and S 2, respectively (see p. 15), Sometimes, S 6 appeared older than the other S (Fig, 395). PC: PC appeared older than the P in 54% of the birds and sometimes the difference in wear was very distinct (Fig. 396 and 399). One bird had PC 2—5 older than the other PC and the P. GC: one bird retained GC 6 and 8. T: in many birds, the T appeared more bleached and sometimes distinctly more abraded than the other remiges, in others one or two T appeared newer than the other wing-feathers (Fig. 400). Hansen (1985) found 21 spring birds (28%, N=75) with mostly one or two, rarely up to five old S: in nine birds S 6 appeared older than the other S, eight birds had one to four mostly central S old (most frequently S 2—3), three birds had S 6 plus one to four central S older than the others and one bird had S 1+6 still growing and S 2—3 old. Among 32 ad autumn migrants in Iberia, one bird had S 2-3+6, one S 2—3 and one S 2 very old (Mead &C Watmough 1976); another bird had P 7-10 older than P 1—6, which is probably due to the resumption of a suspended postbr moult in winter. It appears that S 2—3, which may be retained during the prebr moult, are precisely those occasionally moulted during the postbr moult. Thus it seems that an interrupted prebr S-moult is resumed during the postbr moult. Whether S renewed during the postbr moult are regularly skipped during the prebr moult remains unclear. Those PC that in spring often appear older than the P are more difficult to judge. Since no precise information about the extent and timing
139
of PC-moult is available, it remains unclear whether the PC of some birds are moulted much earlier, just after arriving in the winter quarters, than the rest of the feathers or whether they are not moulted at all during the prebr moult as suggested by their heavy wear (Fig. 396 and 399). It would be interesting to investigate whether or not the state of the PC in spring is age dependent, because ly/2y of a number of species (e.g. Lanins senator, Sylvia communis> Carduelis chloris, C spinus, Loxia curvirostra) which moult P, usually do not renew PC. Those T and S 6 appearing older than the other S in spring could be feathers renewed during the postbr moult which have not been renewed again during the subsequent prebr moult. In this case, however, we would expect differences in wear among the T, since only 27% of those ad renewing T during the postbr moult renew all three. Thus, it may be more probable that the T and S 6 appear older in spring because they have been moulted ahead of the other feathers early after arrival in the winter quarters, the more so because some birds halt prebr moult temporarily after renewal of the T or T and S 6 (Stresemann 1963b). Comments on ageing after prebreeding moult According to present knowledge, 2y and ad cannot be distingushed.
Fig. 393. ly after partial postjuv moult, 16 September. MaC postjuv. MeC 1-4 juv, 5-8 postjuv. GC and rest of wing juv. Recognizable as ly by the fresh plumage and prominent light tips on juv GC, MeC and three juv shoulder feathers.
Fig. 394. 1 y after partial postjuv moult, 12 September. MaC and MeC postjuv. GC 1-8 juv, 9-10 postjuv. Rest of wing juv. Renewed GC 9-10 without light tips, plumage fresh.
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Muscicapa striata
Fig. 395. Ad after partial postbr moult, 7 September. MaC mostly prebr, some postbr. MeC 6 postbr, rest prebr. T postbr. Rest of wing prebr. S 6 appears older than S 1-5 (see text) (P 10 albinotic). Recognizable as ad by the worn plumage, the renewed T and the absence of light tips on GC. Fig. 396. Ad after partial postbr moult, 10 August. MaC and MeC partly prebr, partly postbr. GC 1-8+10 prebr, 9 postbr. T 7-8 postbr, 9 prebr. Rest of wing prebr, but PC appearing older than theP (see text). Recognizable as ad by the worn plumage, the moult limit within T and the absence of light tips on GC.
Fig. 397. 2y/ad after complete prebr moult, 8 May. Whole wing prebr. Whole wing similarly worn. No moult limits. Ageing not possible.
Fig. 398. 2y/ad after interrupted prebr moult, 12 May. Whole wing prebr except S 2â&#x20AC;&#x201D;3. S 2â&#x20AC;&#x201D;3 have been acquired during the last postbr or the preceding prebr moult. Ageing not possible.
Fig. 399. 2y/ad after complete prebr moult, 9 May. Whole wing prebr, but PC older than P. During the prebr moult, the PC have either been renewed ahead of the other feathers or not at all. Ageing not possible.
Fig. 400. 2y/ad after complete prebr moult, 13 May. Whole wing prebr, but PC older than P, GC 10 newer than the other GC and T 8 newer than the other T. Ageing not possible.
Ficedula hypoleuca
141
Ficedula hypoleuca Pied Flycatcher Extent of postjuvenile moult Body-feathers: 8.4% retain individual juv body-feathers, especially uppertail-coverts. MaC: usually all. Exceptionally individual juv MaC may be retained. MeC: about 50% moult all, 50% only part or rarely no MeC. GC: range 0-4, mean 1.5, mode 2, no GC 8.7% (N=1849). T: none 99.2%, one (T 9) 0.8% (N=1091). The extent of GC-moult differs significantly among sexes: 7.1% of cT moult none, 27.3% one, 55.0% two and 10.6% three or four GC (N=282), while the respective percentages for ? are 10,9%, 47.0%, 36.5% and 5.6% (N=285). During the autumn migratory season, there is no significant change in the extent of postjuv moult (Fig. 402). In Sweden, the extent of GC-moult is not significantly different from that found for migrants in Switzerland (Karlsson et aL 1986b; only GC 1-9 recorded, N=182): 48.6% (Switzerland 45.7%) had retained juv GC 1-9, 44.8% (47.1%) GC 1-8, 6.6% (6.7%) GC 1-7, 0% (0.6%) GC 1-6. As found in Switzerland, 8 in Sweden moult significantly more GC than 9. In NW Russia, most ly moult one or two GC (range 0—4) as well as part or all MeC, tail-coverts and MaC (Rymkevich 1990). Postjuv moult is more extensive in early-hatched than late-hatched birds (Rymkevich 1990). Extent of postbreeding moult Usually whole plumage, but among 567 ad migrants examined on Col de Bretolet during the entire migratory seasons of 1988-1992, 15% retained one to four inner S (Fig. 409 and 410). Interruption of Pmoult was not observed. Altogether, 106 ad with interrupted S-moult were recorded in Switzerland, of which 60.4% retained S 6, 21.7% S 5-6, 10.4% S 4-6, 5.7% S 5, one bird S 4-5 and one bird S 3-6 (see p. 15). Asymmetries between left and right wing were frequent. Occasionally, some MeC and MaC were retained and in one bird T 7-8. The proportion of ad with interrupted S-moult increased from 4.5% in August to 27.8% in September on Col de Bretolet. This might indicate that migrants originating from N Europe interrupt S-moult more frequently than birds from central Europe, because northern birds migrate through Switzerland later in the season than central European birds, at least in ly (Jenni 1987).
Fig. 402. Extent of GCmoult during autumn in ly Ficedula hypoleuca after completion of the postjuv moult (data grouped in five-day periods; the first bar includes the period 30 July—8 August, the last 23 September—7 October). White = no GC moulted, wide hatching = one GC moulted, narrow hatching = two to four GC moulted.
Fig. 401. Extent of postjuv moult on the wing and tail in ly Ficedula hypoleuca.
In NW Russia, 22.2% (N=18) retained S 6 or S 4-6 or some MeC (Rymkevich 1990). Other studies found a considerably smaller proportion of ad with interrupted S-moult: four out of 57 ad in S Finland (Hyytia & Vikberg 1973) and four out of 421 ad in Iberia (Mead & Watmough 1976). In August, but not in September, migrants are occasionally caught at the end of P- and S-moult (P 9 almost full-grown, S (3—4) 5—6 growing), indicating that migration may start during the last stages of moult. Moult during the beginning of autumn migration was also observed in Finland (Hyytia & Vikberg 1973). Comments on ageing after postjuvenile and postbreeding moult Best criteria: Moult limit within GC or shape of white tip on innermost juv GC diagnostic of ly. Usually also shape of white tip on T and colour of inside of upper mandible. Skull pneumatization until the end of August (p. 205). ly: In most ly, T show broad white fringes, which are terminally broader on the outer web than the inner web, thus forming a step (Fig. 405) or even a triangle (Fig. 406) on the tip. This is especially conspicuous on T 8. Because not all ly show this pattern clearly (Fig. 407) or moult T, the GC should also be checked. 91.3% of ly show a moult limit within the inner GC which is easily recognized (Fig. 405^07). Inner juv GC have large, whitish tips, often extending along the shaft (Fig. 404). Postjuv GC have whitish fringes, often tinged brownish, no terminal tips and slightly darker and glossier feather centres than juv GC. ly with no GC moulted are easily recognized by whitish tips on inner GC and occasionally by retained juv MeC which are distinguished from postjuv MeC by larger and more whitish terminal fringes or tips (Fig. 404). The inside of the upper mandible is usually light pinkish-grey. In September, ly with grey insides of upper mandibles appear, which are indistinguishable from ad on this criterion (Karlsson et aL 1986b, own data). About 8% of ly are recognizable by buffish tipped juv bodyfeathers, especially uppertail-coverts. Ad: T, especially T 8, terminally with only narrow whitish fringes and no whitish tips (Fig. 409 and 410). Inner GC fringed whitish, often tinged brownish, but without light tip. After the postbr moult, some $ have black outer GC and sometimes MaC, already adjusted to the oncoming breeding plumage. These contrast strongly with the inner non-breeding-plumage-like brown GC and may simulate a moult limit (Fig. 408). Birds having one or a few retained bleached S are ad (Fig. 409 and 410). Inside of upper mandible usually black or dark grey, occasionally grey and indistinguishable from ly.
142
Ficedula hypoleuca
Extent of prebreeding moult: 2y and ad MaC: 76.1 % renew none, 21.5% some (rarely up to three quarters) and 2.4% all MaC (N=376). MeC: 44.1% moult none, 51.9% some central (mostly one to five) and 4%allMeC(N=376). GC: range 0-9, mean 6.5, mode 6, no GC 0.5% (N=382). T: none 0.3%, one 1.0%, two 1.0%, three 97.7% (N=382). R: regular moult of R is rare. We observed one bird with both R 1 renewed and another with symmetrically renewed R 1-5. Ojanen (1987) suggests occasional R-moult in 2y. S: 52.3% moult none, 35.9% S 6 (Fig. 416), 11.0% S 5-6 (Fig. 413), two birds S 4-6 and one bird S 3-6 (N=382) (see p. 15). Asymmetries between left and right wing are frequent. The prebr moult is considerably more extensive than the postjuv moult. There are significant differences between the sexes and age classes in the extent of S-moult: at least one S is moulted by 35% of ad S and 34% of ad ?, but by 67% of 2y 6 and 57% of 2y 9 (N-345). The extent of GC-moult is not significantly different between sexes and age classes. Since the proportion of ad renewing inner S during the prebr moult is high, S retained during the postbr moult are usually moulted during winter. We found only two birds out of 151 ad with very worn S 6 and S 5—6 (Fig. 417), respectively, suggesting that S retained during the postbr moult have not been moulted during the prebr moult either. As 2y renew inner S even more regularly than ad during the prebr moult and since the proportion of ad moulting S during the prebr moult is higher than the proportion retaining S during the postbr moult, the winter renewal of S cannot simply be interpreted as the completion of a suspended S-moult. It rather suggests that inner S are often renewed one moult ahead of the other remiges, 'foreseeing' the possibility that the postbr moult may be interrupted (see also p. 21). It would be interesting to examine whether the percentages of ad with retained S after the postbr moult and with prebr S change concomitantly with latitude. Spring birds without renewed S often have S 6 more bleached than S 5 (Fig. 414). This is probably not due to retaining S 6 during both the postbr and prebr moult, but rather to the fact that S 6 is more exposed during the prebr T-moult than S 1—5. If the T are moulted in a very bright, sunny environment, this might be sufficient to create a difference in bleaching between S 6 and S 5In some cJ, the outer two to four GC and some MaC acquired during the postbr moult are already black, adjusted to the oncoming breeding plumage. These are precisely the coverts usually not moulted during the prebr moult.
Fig. 403. Extent ot prebr moult on the wing and tail in ad and 2y Ficedula Irvpolfitca. For differences ber\veen ad and 2v see text.
In Sweden, the extent of prebr moult was similar to our data from migrants in Italy and Switzerland (Karlsson et ai 1986b), but among 237 Swedish birds, four had all GC renewed. In Finland, 39% had one to three GC unmoulted and 61% more than four (Ojanen 1987; N=243). Roselaar (in Cramp & Perrins 1993) reports renewal of all R in 2y 6 which contradicts our observations and those by Karlsson etal. (1986). Comments on ageing after prebreeding moult Ageing spring birds is difficult in some individuals and requires some practice. On the wing, the most useful criterion is coloration and wear of those GC not renewed during the prebr moult. Since juv GC are more bleached than postbr GC, they contrast more conspicuously with the prebr GC than in ad, at least in cj (Fig. 411). Moreover, juv GC usually have larger light tips, especially conspicuous when juv GC 3^ are present (cf. Fig. 412 and 414 with 415 and 416). These light tips may wear off, resulting in a notch. Birds with only one or two (or even none) juv or postjuv GC are more difficult to age. If black outermost GC can be recognized as having not been moulted during the prebr moult, they are diagnostic of ad. Shape and degree of wear of R are helpful in ageing many birds (Karlsson et aL 1986b, Ojanen 1987). In most ad, they are rounded and hardly worn, in 2y more pointed and well worn. In 2y, the juv PC are usually slightly lighter and more pointed than in ad (cf. Fig. 412 with Fig. 416). Similarly, P of 2y are on average lighter and more worn than in ad. A few 2y retain greyish insides of upper mandibles; most are black as ad. The difference in length between P 10 and the wing-tip is smaller in ly/2y than in ad, but a large overlap prevents this criterion being used for all individuals (Lundberg & Alatalo 1992, Winkel & Winkell992). As wear progresses during the breeding season, these criteria become less diagnostic. They have been examined in detail by Karlsson et aL (1986b), Ojanen (1987) and Lundberg & Alatalo (1992) and, if applied in combination, result in about 90% of correctly aged individuals.
Fig. 404. ly after partial postjuv moult, 29 September. MaC postjuv. MeC 1—6 juv, 7—8 postjuv. GC and rest of wing juv. The inner and central juv GC show conspicuous whitish tips which extend to the shaft on the innermost GC. In this bird, GC 10 has a slightly darker feather centre than the other GC, but is recognized as being juv by the whitish tip. Juv MeC have whitish fringes, the inner juv MeC whitish tips. In postjuv MeC, the fringe is less conspicuous brownish or greyish.
Ficedula hypoleuca
Fig. 405. ly after partial postjuv moult, 5 August. MaC postjuv, MeC postjuv. GC 1-9 juv, 10 postjuv. Rest of wing juv. Recognizable as ly by the moult limit within GC. The renewed GC 10 has no whitish tip, but a brownish fringe and is slightly darker and glossier than the adjacent juv GC. The white fringe at the tip of T 8 forms a distinct step, typical of juv T.
Fig. 406. ly after partial postjuv moult, 10 September. MaC postjuv. MeC postjuv. GC 1—8 juv, 9—10 postjuv. Rest of wing juv. Moult limit within GC and whitish tips on T conspicuous. The renewed GC 9-10 lack a whitish tip and are darker than the juv GC. This bird shows very conspicuous triangular white tips extending along the shaft on inner juv GCandT.
143
Fig. 407. ly after partial postjuv moult, 1 September. MaC postjuv. MeC postjuv. GC 1-7 juv, 8-10 postjuv. Rest of wing juv. Moult limit within GC and pattern on T less typical. The renewed GC show no whitish tips, but only brownish fringes and contrast with the juv GC which have triangular whitish tips. The T, although very probably juv, show no distinct step of the white terminal fringe and resemble very much those of ad.
Fig. 408. Ad cT after complete postbr moult, 31 August. Whole wing postbr. In some 6, the outer GC (in this bird GC 1—4) and some MaC, which are usually not moulted during the prebr moult, do not acquire the brownish colour typical of the non-breeding plumage, but are already black, adjusted to the oncoming breeding plumage. This may simulate a moult limit.
144
Ficedula hypoleuca
Fig. 409. Ad <$ after interrupted postbr moult, 11 September. S 6 and one outer MeC have been retained. All GC with light terminal fringes tinged brownish, but no light tips. Fringe on T terminally narrow without forming a step. The retained S 6 is slightly longer and bleached.
Fig. 412. 2y 9 after partial prebr moult, 3 May. MaC postjuv. MeC 5 prebr, rest juv. GC 1-5 juv, 6-10 prebr. T prebr. Rest of wing juv. Recognizable as 2y by the large white tips on GC 1-5. Among 9, the contrast between juv and prebr GC is only slightly more pronounced in 2y than in ad. This bird also retained juv MeC 1—4 with their white tips. PC more pointed and worn than in ad (cf. Fig. 416).
Fig. 413. 2y c? after partial prebr moult, 28 April. MaC mostly prebr, some postjuv. MeC 1-3 postjuv, 4-8 prebr. GC 1—3 juv, 4-10 prebr. T 7-9 prebr. S 5-6 prebr. Rest of wing juv. Extensive prebr moult including part of the MaC, MeC and S. Recognizable as 2y by the worn and bleached GC, PC and P. Juv GC 3 shows only a very small light tip. Fig. 410. Ad $ after interrupted postbr moult, 14 September. S 4—6 and three MeC have been retained. GC and T without distinct light tips, and with only light fringes. The retained S 4—6 are conspicuously bleached and worn.
Fig. 411. 2y S after partial prebr moult, 26 April. MaC postjuv. MeC postjuv. GC 1—4 juv, 5—10 prebr. T prebr. Rest of wing juv. Recognizable as 2y by the very bleached juv GC contrasting strongly with the prebr GC. PC worn and pointed. This bird shows only small whitish tips on the juv GC, diagnostic only on GC 4, and would have been difficult to age according to this criterion if it had moulted one more GC.
Fig. 414. 2y $ after partial prebr moult, 3 May. MaC postjuv. MeC postjuv. GC 1—4 juv, 5—10 prebr. T prebr. Rest of wing postjuv. Recognizable as 2y by the large white tips on the juv GC 3-4. In 2y 9, the contrast between juv and prebr GC is less pronounced than in 2y S. S 6 is slightly more worn and bleached than S 1—5, although of the same feather generation (juv). This phenomenon is also observed in ad and in other species which renew T during the prebr moult (see text).
Ficedula hypoieuca
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Fig. 415. A d d after partial prebr moult, 11 June. MaC mostly postbr, some prebr. MeCpostbr. GC 1-4 postbr, 5-10 prebr. T prebr. Rest of wing postbr. The GC not renewed during the prebr moult contrast less with the prebr GC than in 2y and have no or only faint light tips, thus are diagnostic of ad. PC less worn and more rounded than in 2y.
Fig. 416. Ad 9 after partial prebr moult, 5 June. MaC postbr. MeCpostbr. GC 1-4 postbr, 5-10 prebr. T prebr. S 6 prebr. Rest of wing postbr. Tips of PC rounded and less worn than in 2y(cÂŁFig.4l2).The contrast between moulted and unmoultcd GC is slight, hardly less pronounced than in 2y (cf. Fig. 412 and 414).
Fig. 417. Ad 9 after partial prebr moult, 10 May. MaC, MeC and GC postbr. T 8 prebr. T 7+9 postbr or even older. S 5-6 retained during the prebr and the preceding postbr moult. Rest of wing postbr. Rare case of a prebr moult of limited extent. This bird did not moult S 5â&#x20AC;&#x201D;6 during both the prebr and preceding postbr moult.
146
Pants ater
Parus ater Coal Tit Extent of postjuvenile moult MaC and MeC: usually all. ly with no GC moulted may retain individual juv MeC or MaC. GC: range 0-10, mean 6.3, mode 7, no GC 1.4%, all GC 1.2% (N=2780). CC: 9.8%. Al: none 93.2%, one 6.8% (N=1009). T: none 93.6%, one 3.3%, two 2.2%, three 1.0% (N=732) (seep. 33). R: one bird with renewed GC 3-10, Al 1, CC and T 8â&#x20AC;&#x201D;9 also moulted R 1 on both sides, The extent of postjuv moult is correlated among GC, CC, Al and T (Fig. 419). CC, Al and T may be renewed when at least six GC are moulted. At the end of the autumn migratory season, birds show significantly fewer GC moulted (Fig. 420). Besides this, there are significant differences among years in the number of GC moulted which are positively correlated with the total number of birds caught on Col de Bretolet. This suggests that during years of Coal Tit eruptions, birds fledged earlier than the Alpine population pass by on migration. On Col de la Goleze, France (3km west of Col de Bretolet), the extent of GC-moult was similar to that on Col de Bretolet (Frelin 1969): the mean number of GC moulted was 6.5 and ly with all GC moulted were estimated to be less than 2% (N=l604). Again a similar extent of GC moult was recorded in England (mean 6.6 GC renewed; N=l45)> and birds from northern and eastern study sites had slightly less GC moulted than birds from southern sites (Christmas et ai 1989). In NW Russia, 2.1% moult all GC, 1.3% none, the rest one to nine, most frequently (76.6%) six to eight (N=613); surprisingly, most birds were recorded as renewing the CC and 82.2% all Al feathers, 11.6% part and only 6.2% none (Rymkevich 1990). According to Scherrer (1972), 30% of ly moult Al feathers on Col de la Goleze, which seems a very high percentage. Svensson (1992) reports that Al feathers are never moulted, probably referring to northern birds.
Fig. 419. Relationships between the number of postjuv GC and the percentage of individuals with renewed CC, Al and T in ly/2y Parus ater which have completed their postjuv moult.
Fig. 420. Mean number of postjuv GC during autumn of ly Parus ater which have completed the postjuv moult (data grouped in five-day periods; the first value includes the period 29 Augustâ&#x20AC;&#x201D;~" September, thelast 28 October-6 November).
Fig. 418. Extent of postjuv moult on the wing and tail in ly/2y Parus ater.
Extent of postbreeding moult Whole plumage. Comments on ageing Best criteria: Skull pneumatization until mid-October (p. 206). Moult limits within GC, within MeC and difference in colour between GC, MeC and PC. ly/2y: 97.4% show a moult limit within GC, which is relatively easy to recognize. The renewed GC are darker and fringed bluish-grey, juv GC are lighter and fringed greenish-grey (Fig. 424). ly with no or only one or two GC moulted can be recognized by a distinct difference in colour of feather centres and fringes between the juv GC and the postjuv MeC (Fig. 423) and sometimes by a moult limit within MaC and MeC (Fig. 422). ly with all GC moulted are more difficult to distinguish from ad: they show a contrast in colour between postjuv GC and juv PC which is more pronounced than in ad (Fig. 426); some of them can also be recognized by a moult limit within T (Fig. 425) or Al, or by a renewed CC which contrasts with the juv PC (Fig. 426). Ad: No moult limits within MeC, GC, Al and T. All GC fringed bluish-grey, not greenish. Difference in colour between GC and PC only slight (Fig. 427).
Fig. 421. ly in juv plumage, 31 July. Whole wing juv. Note the loose texture and the greenish tinge of MaC and MeC.
Parus ater
147
Fig. 422. 1 y after partial postjuv moult, 30 October. Inner MaC postjuv, outer juv. Outer four MeC juv, inner two postjuv. GC and rest of wing juv. Rare case of a bird with limited postjuv moult. Recognizable as ly by moult limits within MaC and MeC.
Fig. 425- ly after partial postjuv moult, 25 October. MaC and MeC postjuv. GC 1 juv, 2—10 postjuv. CC postjuv. Al 1 postjuv, 2—3 juv. T 7 juv, 8—9 postjuv. Rest of wing juv. Recognizable as ly by the retained juv GC 1 fringed greenish and the moult limit within T. Fig. 423. ly after partial postjuv moult, 27 October. MaC and MeC postjuv. GC 1-8 juv, 9—10 postjuv. Rest of wing juv. Moult limit within GC and difference in colour between juv GC and postjuv MaC and MeC diagnostic of ly. The renewed GC 9—10 are darker than the juv GC and fringed bluishgrey.
Fig. 426. ly after partial postjuv moult, 4 September. MaC and MeC postjuv. GC postjuv. CC postjuv. Al 1 postjuv, 2—3 juv. T postjuv. Rest of wing juv. The difference in colour between the juv PC and the postjuv GC, CCandAl 1 is more pronounced than in ad (c£ Fig. 427).
Fig. 424. ly after partial postjuv moult, 1 November. MaC and MeC postjuv. GC 1-6 juv, 7—10 postjuv. Rest of wing juv. Distinct moult limit within GC. Juv GC lighter and fringed greenish, postjuv GC darker and fringed bluish. Fig. 427. Ad after complete postbr moult, 16 September. Whole wing postbr. No moult limits within GC, T and Al. Only slight differences in colour among GC, CC, Al and PC.
148
Parus caeruleus
Parus caeruleus Blue Tit Extent of postjuvenile moult
MaC and MeC: all. GC: range 5-10, mean 9.9, mode 10, all GC 94.1% (N=1957). CC: 96.1%. Al: none 2.9%, one 14.1%, two 14,6%, three 68,4% (N=1120). T: none 2.1%, one 1.7%, two 26,4%, three 69.8% (N=1109) (see p. 33). R: none 25.5%, one 69.9% (R 1), two 2.7% (R 1-2), three to five 1.4%, six 0.5% (N=1092) (see p. 34). S: one bird with all GC, CC, Al, T and R 1 moulted also renewed S 6 on both wings. Near Rome, one bird was found with S 5-6 and all R renewed (Fraticelli & Gustin 1987a). The extent of postjuv moult is correlated among GC, CC, Al, T and R (Fig. 429). All T and all Al may be renewed when at least nine GC are moulted. There is a tendency for the extent of postjuv moult to be smaller in ? than in cT, although this is not significant in our data (N=383). On Col de Bretolet, there are significant differences in the extent of GC-, Al- and T-moult between years. A similar extent of R-mouIt was found in the Netherlands (Roselaar in Cramp & Perrins 1993) and of GC- and Al-moult on Col de la Goleze, France (3km west of Col de Bretolet) with no significant differences between sexes and some non-significant variation between years (Frelin 1977). In NTW Russia, the extent of postjuv moult is roughly similar to our data: 63.8% renewed R 1, 0.4% R 1+2, 79.9% all Al, 92.4% all T and 96.5% all GC, while only two birds retained tailcoverts and MeC (N=536). In England, the extent of postjuv moult is smaller than in central Europe and NW Russia: about one third of ly retain one to six juv GC, only 15% renew R 1 and about half of ly moult the Al (Flegg & Cox 1969). According to Spencer & Mead (1978a), one third at most moult all GC, CC and Al, compared to 68% in our data and in those of Frelin (1977). In Mediterranean birds, small samples suggest a more extensive postjuv moult (Roselaar in Cramp & Perrins 1993). According to Rymkevich (1990), earlyhatched birds perform a more extensive postjuv moult than those hatched later. Variation in the extent of postjuv moult between years is also reported from England (Spencer & Mead 1978a, without statistics) and Germany (Reith & Schmidt 1987).
Fig. 428. Extent of postjuv moult on the wing and tail in ly/2y Parus caeruleus.
Extent of postbreeding moult Whole plumage. Comments on ageing Best criteria: Difference in colour between postjuv GC and juv PC diagnostic of ly. Skull pneumatization until mid-October (p. 206). ly/2y: Ageing up to the first postbr moult presents no difficulties. Moult limits within GC (6% of ly; considerably more in Great Britain) are conspicuous (Fig. 431 and 432). ly with all GC renewed (94%) are recognizable by a marked difference in colour between GC and PC. The outer webs of the postjuv GC are blue, those of the juv PC bluishgrey, often tinged greenish. The PC also contrast with the mostly renewed CC and Al, in their duller colour (Fig. 433 and 434). Ad: No, or only a slight, difference in colour between GC and PC (Fig. 435). No moult limits within GC, Al, T and R.
Fig. 429. Relationships between the number of postjuv GC and the percentage of individuals with renewed CC, Al, T and R in ly/2y Parus caeruleus which have completed'their postjuv moult.
Fig. 430. ly in juv plumage, 14 June. Whole wing juv.
MaC and MeC greenish, not blue. All GC bluish-grey like the PC.
Parus caeruleus
Fig. 431. ly after partial postjuv moult, 26 October. MaC and MeC postjuv. GC 1 juv, 2—10 postjuv. CC juv. Al 1 postjuv, 2—3 juv. T 7 juv, 8—9 postjuv. Rest of wing juv. Distinct moult limit within GC. Juv GC 1 bluish-grey like the PC, not blue like the postjuv GC. Fig. 432. ly after partial postjuv moult, 25 September. MaC and MeC postjuv. GC 1-5 juv, 6—10 postjuv. Rest of wing juv. ly with five juv GC and retained CC and Al which are bluish-grey like the juv PC, not blue like the renewed MaC, MeC and GC 6-10.
149
Fig. 433. ly after partial postjuv moult, 22 October. MaC and MeC postjuv. GC postjuv. CC postjuv. Al postjuv. T postjuv. Rest of wing juv. Distinct difference in colour between the juv PC and the postjuv GC, CC andAl.
Fig. 434. 2y after partial postjuv moult, 24 April. MaC and MeC postjuv. GC postjuv. CC and Al postjuv. T postjuv. Rest of wing juv. In spite of marked abrasion, the difference in colour between postjuv coverts and juv PC is still conspicuous.
Fig. 435. Ad 6 after complete postbr moult, 13 October. Whole wing postbr. Outer webs of PC and GC of the same blue colour. No moult limits within GC, Al and T.
150
Parus major
Parus major Great Tit Extent of postjuvenile moult MaC and MeC: all. GC: range 7-10, mean 9.96, mode 10, all GC 97.1% (N=586). CC: 96.2%. Al: none 4.4%, one 42.9%, two 21.8%, three 30.9% (N=340). T: none 1.5%, one 2.3%, two 27-9%, three 68.3% (N=34l) (see p. 33). R: none 2.2%, one to five 7.1%, six 90.8% (N=325) (see p. 34). S: two ly with all GC, CC, Al, T and R renewed had S 6 moulted on both wings, two other ly had S 6 and one ly S 5-6 renewed on one wing only. Dhondt (1973) has also found two birds among 136 with partially renewed inner S.
The few birds which retain GC are more likely to retain juv T, R, CC and Al than ly with all GC moulted. The extent of postjuv moult differs according to sex, population, fledging date and year. <$ perform a significantly more extensive postjuv moult than 9 (Fig. 437). A very similar extent of postjuv moult as in Switzerland was found in Frankfurt, Germany (Reith & Schmidt 1987) and in Belgium (Dhondt 1973): more than 93% renew all GC, more than 83% all R, more than 97% the CC, around 30% all Al and most birds all T (cf. Roselaar in Cramp & Perrins 1993 for Al-moult in the Netherlands). In England, however, the proportion of birds moulting all GC and Al was lower (Flegg & Cox 1969, Gosler 1991): in Oxfordshire, only 70% moult all GC and in Kent about 80% renew all R, but apparently none the Al; in Hertfordshire, only 8% renew part or the whole Al and
Fig. 436. Extent of postjuv moult on the wing and tail in ly/2y Parus major.
slightly more than 80% all GC. Birds from the Baltic area have a significantly smaller extent of postjuv moult than in Germany (Reith & Schmidt 1987). However, Rymkevich (1990) reports an extensive postjuv moult, especially for Al and R (see Fig. 437), from NW Russia (91% of c5, N=446, and 85% of 9, N=546, renew the CC). In S Sweden, 65% renew all R (N=99), 12% all Al on both wings, 7% on one wing only and 88% all GC (N=214; A.A. Dhondt in lift.). These figures are lower than in Belgium, Switzerland and Germany. In Ottenby, Sweden, the proportion of birds moulting the Al (8â&#x20AC;&#x201D;46%, depending on year and site; only Al 1â&#x20AC;&#x201D;2 examined) was significantly lower than in the Baltic area; furthermore, seven out of 1039 ly apparently moulted one to five inner PC (Pettersson 1981). Mediterranean birds seem to renew the Al more often than elsewhere (Roselaar in Cramp & Perrins 1993); they should also be checked for renewal of S and P. Birds fledged late in the season (mainly second broods) start moulting at an earlier age (as shown for R-moult by Dhondt 1973; Rymkevich 1990) and moult less extensively than birds fledged early, as shown for Al in Belgium, Germany and NW Russia, T in NW Russia and GC in Germany and England (Dhondt 1973, Reith & Schmidt 1987, Rymkevich 1990, Gosler 1991). Furthermore, significant differences in the extent of postjuv moult occur between years at the same site (Rymkevich 1990), between nearby sites and between local birds and immigrants (Reith & Schmidt 1987). The marked variation between years prevents the use of the extent of postjuv moult for generally determining the proportion of immigrants from areas with different moult characteristics (Petterson 1981, Reith & Schmidt 1987). Extent of postbreeding moult Whole plumage. Comments on ageing Best criteria: Skull pneumatization until October (p. 206). Difference in colour between GC and PC, moult limits within Al, GC, T and R.
Fig. 437. Percentage of 6 and 9 ly/2y Parus major which have renewed all R, all GC and all Al after completion of the postjuv moult for different study areas (numbers below columns denote sample sizes; stars denote significant differences (P < 0.05) between the sexes). CH = various sites in Switzerland (own data); G = Schluchtern near Frankfurt, Germany (Reith & Schmidt 1987); B = Ghent, Belgium (Dhondt 1973); GB - Oxford, England (Gosler 1991); Baltic = eastern Baltic area (Reith & Schmidt 1987); Russia = NW Russia (Rymkevich 1990); Ottenby = Oland, Sweden (Pettersson 1981); S = South Sweden (A.A. Dhondt in lift.), At sites B and S, only Al 3 was examined among the three Al feathers (birds with Al 3 renewed on one wing only counted as half) and GC only when Al 3 was old; for this graph, we assumed that birds with a renewed Al 3 had all Al and GC moulted, as shown to be the case in all Swiss birds.
ly/2y: Ageing Great Tits is more difficult than Blue and Coal Tits. Since only 3% show a moult limit within GC, which is always conspicuous when present (Fig. 439), the difference in colour between postjuv GC and juv PC is the main ageing criterion. The outer webs of the juv PC are less intensely blue (sometimes tinged greenish), thus contrast more with the bluish postjuv GC than in ad (cf Fig. 441 and 443). This is more pronounced in S than in 9. 43% of ly show a moult limit between Al 1 and 2 (Fig. 440 and 441). The juv Al 2 is less intensely blue than the postjuv Al 1. Moult limits within T (30%) and R (7%) may also be of help and are recognizable mainly by differences in wear (Fig. 440).
Parus major
Ad: Outer webs of GC and PC almost of the same intense blue colour. No difference in blue tinge between Al 1—2 and PC. No moult limits within GC, Al, T and R.
151
Fig. 441. ly cT after partial postjuv moult, 26 October. MaC and MeC postjuv. GC postjuv. CC postjuv. Al 1 postjuv, 2-3 juv. T postjuv. Rest of wing juv. The juv PC and Al 2-3 are less intensely blue than the renewed MaC, MeC, GC, CC and All.
Fig. 438. ly In juv plumage, 23 July. Whole wing juv. MaC, MeC and GC only faindy tinged blue, typical of juv plumage.
Fig. 439. 2y 9 after partial postjuv moult, 10 March. MaC and MeC postjuv. GC 1—2 juv, 3—10 postjuv. Rest of wing juv. Rare case of a 2y with a moult limit within GC. The juv GC contrast conspicuously with the postjuv GC in their lack of blue and their greyish feather centres.
Fig. 442. 2y 9 after partial postjuv moult, 30 April. MaC and MeC postjuv. GC postjuv. CC and AJ postjuv. T postjuv. Rest of wing juv. In spring, the difference in colour between the postjuv GC and the juv PC is slightly more pronounced due to wear. T 7, although postjuv, is slightly greyer than the postjuv T 8-9 (cf. Fig. 440).
Fig. 443. Ad <J after complete postbr moult, 17 October. Whole wing postbr. PC and Al have almost the same blue colour as MaC, MeC, CC and GC.
Fig. 440. 2y <5 after partial postjuv moult, 16 April. MaC and MeC postjuv. GC postjuv. CC postjuv. Al 1 postjuv, 2—3 juv. T 7 juv, 8—9 postjuv. Rest of wing juv. Distinct difference in colour between juv PC and postjuv GC as well as moult limits within Al and T are diagnostic of 2y.
Fig. 444. Ad 9 after complete postbr moult, 29 April. Whole wing postbr. 9 are generally less intensely coloured than $. Towards spring, wear is comparatively slight.
152
Sitta europaea
Sitta europaea Nuthatch Extent of postjuvenile moult MaC: usually all. A few birds retain some juv MaC in the distal part of the wing. MeC: 0-8, mean 4.7, mode 5. Most birds (93%) moult three to six MeC (N=40). GC: usually not moulted. Only two birds out of 40 renewed GC 10 on one wing. Extent of postbreeding moult
Fig. 445. Extent of postjuv moult on the wing in ly/2y Sitta europaea.
Whole plumage (Matthysen 1986). Comments on ageing Best criteria: Although the Nuthatch is one of the very few passerines never attaining a fully pneumatized skull in ad, skull pneumatization and the examination of the MeC are up to now the only valuable criteria for ageing. Skull pneumatization scores 1—5 indicate ly (p. 206). Birds with score 6 can be either ly/2y or ad. As skull pneumatization proceeds very slowly, all ly and ad can be separated through November and most through December. ly/2y: Over 90% show a moult limit within the MeC. Outer juv MeC are greyish brown with only a faint blue tinge or, when abraded and bleached, no blue at all. Renewed inner MeC are as blue as the MaC and the scapulars. Dark centres on the outer four MeC can occur in juv and postjuv MeC. Moreover, after postjuv moult there is always a slight difference in the intensity of the blue tinge between the juv GC and the postjuv scapulars and other body-feathers. Ad: No moult limit within the MeC. No difference in the intensity of the blue tinge between body-feathers and GC, <J being more intensely coloured than 9. Fig. 446. ly in juv
plumage, 28 May. Whole wing juv. MaC and MeC greyish not blue* especially the inner four MeC.
Fig. 448. ly after partial postjuv moult, 15 December. MaC postjuv. MeC 1—3 juv, 4-8 postjuv.GC 1-9 juv, 10 postjuv. Rest of wing juv. Moult limit within MeC and GC
diagnostic of ly. The fringes of the juv MeC 1—3 are greyish, not blue as in the postjuv MeC and MaC. The
renewed GC 10 is distinctly more blue than the juv GC 1-9.
Fig. 449. 2y after partial postjuv moult, 3 August. MaC postjuv, except the outermost. MeC 1-3 juv, 4-8 (mostly hidden) postjuv. Rest of wing juv. The juv MaC and MeC
are very bleached and contrast with the postjuv MeC.
Fig. 447. 2y after partial postjuv moult, 25 February. MaC postjuv, except the most distal ones. MeC 1-4 juv, 5-8 postjuv. GC and rest of wing juv. Recognizable as 2y by the moult limit within MeC. Juv MeC 1-4
less blue and more abraded than inner four MeC and the MaC.
Fig. 450. Ad after complete postbr moult, 6 September. Whole wing postbr. All wing-coverts show the same blue tinge.
Oriolus oriolus
Oriolus oriolus Golden Oriole
153
Although the number of birds examined is still small, the percentage of 36% of ad with renewed S in autumn (Mead & Watmough 1976) corresponds well with the 38% that retained S in spring. Comments on ageing after the prebreeding moult
Extent of postjuvenile moult Most Golden Orioles have ten S, 11 GC and nine MeC, some birds 11 S, 12 GC and ten MeC. Body-feathers: usually all, but quite regularly, some juv scapulars and exceptionally some juv body-feathers (e.g. on the neck) are retained. MaC: generally all. A few ly retain some central MaC in the undermost row. MeC: mean 1.5, none 15.4%, one 30.8%, two 46.2%, three 7.7% (N=13). MeC are moulted from inside to outside. GC: mean 1.3, none 30.8%, one 23.1%, two 30.8%, three 15.4% (N=13). GC 11 or 12, respectively, may remain unmoulted out of sequence, as GC 10 in other passerines.
Apart from the easily recognized ad cT with overall yellow and black plumage without streaking or mottling of underparts, ageing and sexing in spring is not easy. 2y are said not to change their plumage design markedly during the first prebr moult. They look like ly birds and keep their distinct streaking of underparts (Svensson 1992). This may distinguish them from a large part of the ad ? which have only faintly streaked or mottled underparts. However, there is still some overlap, especially between 3y 3 and ad ? with cJ-like appearance. Extension and pattern of yellow marks on PC as well as extension of yellow along the tips of the outermost R are also helpful criteria (see Svensson 1992). The retention of S (Fig. 453) is not an ageing criterion, as it occurs in both ad and 2y, although 2y retain S more frequently and in larger numbers than ad.
Extent of postbreeding moult Partial moult of variable extent. Some ad only renew some bodyfeathers, a few MaC and one or two MeC, but not the rest of the wing. Others moult all body-feathers, part of MaC, MeC and GC as well as T and, according to Ginn & Melville (1983), central R. Mead & Watmough (1976) found four out of 11 birds (36%, cf. prebr moult) which replaced inner S (mean 2.3), but no P. On the other hand, one ad from Col de Bretolet had renewed P 1 on both wings, together with T 8-10, GC 7, half of the MaC and MeC as well as the entire body plumage while the rest of the wing and the rectrices were old. Another ad from Col de Bretolet renewed S 1+5 on the right (Fig. 452) and P 1 on the left wing. A 2y ? from Malta (Natural History Museum, Basel) renewed only part of the body-feathers during the postbr moult and also retained the juv S 4-6 already retained during the preceding prebr moult. Comments on ageing after postjuvenile and postbreeding moult
Fig.451. ly after partial postjuv moult, 1 September. MaC postjuv. MeC 1-7 juv, 8â&#x20AC;&#x201D;9 postjuv. GC 1â&#x20AC;&#x201D;8 juv, 9â&#x20AC;&#x201D;11 postjuv. Rest of wing juv. Recognizable as ly by the bright yellow fringes on juv MeC. Moult limit within GC conspicuous: postjuv GC dark green, juv GC brownish green.
Best criteria: Fresh plumage and bright yellow fringes on MeC diagnostic of ly. Worn plumage and no bright fringes on MeC diagnostic of ad. ly: Since ly renew at most a few inner MeC, they are always recognizable by brightly yellow fringed outer juv MeC (Fig. 451). Juv GC also show yellow fringes, but often inconspicuous and of individually variable width. Moult limits within MeC and GC are easily recognized. Postjuv GC and MeC are darker green, juv GC and MeC brighter green fringed yellow. Moreover, the flight feathers of ly are hardly worn. Ad: No yellow fringes on MeC. Tips of unmoulted P, R and T worn. If T or S are replaced, they contrast with the old S in their brightness (Fig. 452). Extent of prebreeding moult: 2y and ad Generally whole plumage, but a rather high percentage of ad (38.1%, N=29) and of 2y (83-3%, N=24) retain some inner S. In ad, only one (S 6) or two (S 5-6 or 6-7) S are retained and in most cases on one wing only. In 2y, one to five S may remain unmoulted and in 90% of such cases this occurs on both wings. The percentages of retained S in 2y are: S 6 25%, S 5-6 35%, S 4-6 15%, S 3-6 15%, S 3-7 10% (N=20). One bird with unmoulted S 3-7 also retained all Al and R 5-6. In 2y and ad, we found no retained P.
Fig. 452. Ad $ after partial postbr moult, 23 August. MaC partly prebr, partly postbr. MeC prebr. GC 1-10 prebr, 11 prebr or postbr. S 1+5 postbr, 2-^+6 prebr. T prebr. Rest of wing prebr. Recognizable as ad by the lack of yellow fringes on MeC and by worn tips of
P,TandGC.
154
Oriolus oriolus
Fig. 453. Ad 6 after complete prebr moult interrupted at S 6, 29 April. Whole wing prebr, except postbr S 6. This bird retained S 6 during the prebr moult on the right wing only.
Lanius collurio Red-backed Shrike Extent of postjuvenile moult Body-feathers: only partly moulted. Some ly replace very few or, at least on the upperparts, no body-feathers. MaC: about half of the ly moult part, some all and some no MaC. MeC: 54% moult none, 27% one, 16% two to six and 3% all MeC (N=37). GC: 94.9% moult none, three birds one and one bird two GC in irregular sequence (N=79). T: one ly moulted T 8 (N=79). A partial body-feather moult was also observed in Germany (Kramer 1950) as well as in NW Russia where 65% renew the MeC partially and only 5-7% the tail-coverts (Rymkevich 1990). The Red-backed Shrike is among the very few European passerines in which the feathers acquired during the postjuv moult are markedly different from those of ad (hence termed second juvenile plumage by Stresemann 1963a). This is especially obvious in <5, in which the postjuv feathers of the head and back are brownish with dark subterminal marks, not grey or reddishbrown, respectively. But the postjuv feathers of ly ? also have more conspicuous dark subterminal marks than in ad $ in which these marks may be completely absent.
Fig. 454. Extent of postjuv moult on the wing and tail in ly Lanius collurio.
departure for autumn migration (Rymkevich 1990). In Crete, 63% (N=130) had renewed one to three T (mean 1.5), four birds had interrupted P-moult after renewal of P 1 (two birds), P 1-2 and P 1-5, respectively, and one bird had single S renewed; the proportion of birds with renewed T decreased during autumn migration (Swann & Baillie 1979). In captivity, six paired birds underwent a partial body-feather moult after breeding, while two unpaired birds underwent a complete moult in late summer, which apparendy was also observed in one ad $ skin (Kramer 1950).
Extent of postbreeding moult According to six ad examined after or during the last stages of postbr moult, body-feathers, MaC and MeC are only partly renewed, or not at all. One bird renewed GC 8â&#x20AC;&#x201D;10, four one or two T, three R 1 and one bird had S 6 growing. Body-feathers are known to be only partly renewed in most birds (Kramer 1950). In NW Russia, 5-80% of the body-feathers are renewed, usually only a few, in 17% of 6 and 31 % of $ one to three T and in 2.4% of 9 R 1. However, some ad might not moult at all before
Comments on ageing after postjuvenile and postbreeding moult Best criteria: Fresh plumage and dark subterminal marks on juv coverts as well as on juv and postjuv body-feathers of the upperparts, diagnostic of ly. Skull pneumatization sometimes difficult to recognize in live birds due to the thick scalp, and is valid until the end of August. ly: All ly retain a large proportion of juv wing-coverts and bodyfeathers on upperparts which are recognizable by dark subterminal
Lanius collurio
marks, often crescent-shaped and prominent, but sometimes smaller, especially on T. Ad: Plumage worn. No subterminal dark marks on wing-coverts and T or, in some 9, only inconspicuous ones. Renewed T are characteristic of ad (Fig. 458), but may also occur in ly (Fig. 456). 8 with grey heads are ad. Extent of prebreeding moult: 2y and ad
155
Fig. 457. ly after partial postjuv moult, 14 August. MaC mostly postjuv, a few juv. MeC juv. GC 1—3+5—10 juv, 4 postjuv. Rest of wing juv. Recognizable as ly by the dark subterminal marks on juv GC and MeC.
Whole plumage. The complete moult lasts 80—85 days and occurs between late November and April, mainly in southern Africa (Snow 1965, Pearson 1972, Pearson & Backhurst 1976, Kasparek 1981, B, Bruderer pers. comm.). Among 31 spring migrants and breeding birds, none was found with a moult limit. Thus, feathers renewed during the postjuv and postbr moult are probably moulted again during the prebr moult. Among 19 captive 2y birds, two moulted P eccentrically, leaving P 1—5 and 1—6, respectively, unmoulted (Gwinner & Biebach 1977). This resembles the first prebr moult of 2y L. isabellinus and L. senator (seep. 46). Comments on ageing after the prebreeding moult According to present knowledge, 2y and ad cannot be separated on plumage characters.
Fig. 458. Ad $ after partial postbr moult, 11 August. MaC partly prebr, partly postbr. MeC 1-6+8 prebr, 7 postbr. GC prebr. T 7 prebr, 8-9 postbr. Rest of wing prebr. Recognizable as ad by die worn remiges and GC as well as by the absence of dark subterminal marks on MeC and GC.
Fig. 455. ly in juvenile plumage, 8 August. Whole wing juv. This bird was on migration in complete juv plumage. Recognizable as ly by the dark subterminal marks on wing-coverts and T. Fig. 459. 2y/ad 9 after complete prebr moult, 8 May. Whole wing prebr. Ageing not possible. This 9 shows inconspicuous dark subterminal marks on MeC, inner GC and body-feathers of the upper side.
Fig. 456. ly after partial postjuv moult, 16 August. MaC postjuv. MeC 1+8 postjuv, 2-7 juv. GC juv. T 7+9 juv, 8 postjuv. Rest of wing juv. The subterminal dark marks on juv GC, MeC and T 9 are very prominent and crescent-shaped. This bird, exceptionally, renewed T 8.
Fig. 460. 2y/ad $ after complete prebr moult, 27 April. Whole wing prebr Ageing not possible.
156
Garrulus glandarius
Garrulus glandarius Jay Extent of postjuvenile moult
MaC and MeC: all. GC: range 0-10, mean 6.2, mode 6, no GC 4.2%, all GC 16.7% (N=72). CC: 18.1%. Al: none 47.2%, one 16.7%, two 4.2%, three 31.9% (N=72). T: none 62.2%, one (T 9) 21.6%, two (T 8-9) 16.2% (N=37). R: we found no regular R-moult. The extent of postjuv moult is correlated among GC, CC, Al and T. Al may be renewed when at least five GC are moulted, T when at least six and CC when at least nine GC are moulted, ly with all GC renewed usually have moulted one or two T, the CC and all Al. A similar extent of postjuv moult is reported from France and England: Mayaud (1948) mentions that the postjuv moult includes T, six GC and in about 25% of ly/2y Al; in England about six or fewer GC are replaced, sometimes together with one T (Ginn & Melville 1983). Swedish birds apparently moult neither GC nor Al (Svensson 1992). Birds in NW Russia only rarely moult the innermost GC, never Al and CC and may retain part of the MeC (Rymkevich 1990). Richards' (1976) claim that ly may replace their inner two pairs of P and the central tail-feathers is unusual. Extent of postbreeding moult Whole plumage. Comments on ageing Best criteria: Ageing is based on the pattern of the black bars on the blue GC, CC, Al and PC: the intervals between the black bars on juv feathers are broader than on renewed (postjuv and postbr) feathers. Juv GC 1 shows (occasionally six) seven or eight black bars (black tip not counted), postjuv and postbr GC 1 10-12 (occasionally 13). Since 83% of ly/2y retain at least one juv GC, most ly/2y can be recognized by this criterion. ly/2y with all GC renewed, birds with nine black bars (7% of ad and ly/2y) and birds with disturbed barring should be aged by using the criteria mentioned below.
Fig. 461. Extent of postjuv moult on the wing and tail in ly/2y Garrulus glandarius.
These irregularities are repeated identically on all nine PC (and the unmoulted GC and Al feathers) in ly (Fig. 465 and 466), but occur only on isolated, or at most on two neighbouring, PC in ad (Fig. 468 and 469). Moult limits within the inner black GC and within T are difficult to detect. Postjuv inner black GC are deeper velvet black than juv ones. Moreover, in most cases there is a marked difference in length between the two generations of GC (Fig. 464). Renewed T are broader at the end and deeper black than juv T. Most difficult to separate are ly/2y with all GC, Al and CC renewed from ad without irregularities in the barring of the PC (cf. Fig. 467 and 470). With some experience, however, one can see that in ly/2y the juv PC are more widely barred than the postjuv GC, whereas in ad the bars on PC have approximately the same intervals as those on the GC. An additional criterion has been given by Svensson (1992): the width of R5 taken about 40mm from the tip measures 20â&#x20AC;&#x201D;25 mm in ly/2y and 25-30 mm in ad. Ad: GC 1 with 10-12 (13) black bars (black tip not counted). No moult limit in GC and Al. If barring not disturbed, all blue feathers have bars with the same narrow intervals (Fig. 470). Irregularities in the barring are discontinuous. They occur only on isolated, or at most on two neighbouring, feathers at the same distance from the tip (Fig. 468 and 469).
ly/2y: A moult limit within the blue GC or the Al (Fig. 465) or both (Fig. 464) is shown by 36% of ly. It is recognizable by the difference between narrowly barred postjuv, and broadly barred juv feathers. Most ly can be recognized by examining the pattern of irregularities in the barring (disturbances during feather growth expressed by differences in width of, and intervals between the black bars), which is best checked on PC, because they are never renewed by ly/2y. About 70% of ly and 87% of ad show irregular barring (always check both wings).
Fig. 462. Relationships between the number of postjuv GC and the percentage of individuals with renewed CC and Al in ly/2y Garrulus glandarius which have completed their postjuv moult.
Fig, 463. 2y after partial postjuv moult, 7 January. MaC and MeC postjuv. GC 1-6 juv, 7â&#x20AC;&#x201D;10 postjuv. Rest of wing juv. Recognizable as 2y by the wide barring of the blue feathers. GC 1 with seven black bars. Moult limit between juv GC 6 and postjuv GC 7 very hard to see, GC 7 being slightly darker black.
Garrulus glandarius Fig. 464. 2y after partial postjuv moult, 11 January. MaC and MeC postjuv. GC 1-4 juv, 5-10 postjuv. Al 1 postjuv, 2-3 juv. CC and rest of wing juv. GC 1 with eight bars. Conspicuous moult limit within Al and GC, recognizable by wide barring on juv GC 1-4 and Al 2-3, but narrow barring on postjuv GC 5 and Al 1. Note also the difference in length between juv and postjuv GC.
Fig. 465- 2y after partial postjuv moult, 14 January. MaC and MeC postjuv. GC 1-4 juv, 5-10 postjuv. Al 1 postjuv, 2-3 juv. Rest of wing juv. Irregularities in the barring are repeated identically on all the unmoulted blue feathers and occur at the same distance from the tip. Renewed Al 1 with regular narrow barring and slightly brighter blue than adjacent juv blue Al andGC.
Fig. 466. ly after partial postjuv moult, 6 December. MaC and MeC postjuv. GC, Al and CC postjuv. T 7-8 juv, 9 postjuv. Rest of wing juv. Although all GC, CC and Al have been renewed, this bird can be recognized as ly by the occurrence of identical irregularities in the barring on all PC.
157
Fig. 467. ly after partial postjuv moult, 12 December. MaC and MeC postjuv. GC, Al and CC postjuv, T 7â&#x20AC;&#x201D;8 juv, 9 postjuv. Rest of wing juv. This bird is difficult to age, because there are neither moult limits within GC and Al nor irregularities in the barring of the blue feathers. With experience, however, one can see that the juv PC have slightly larger intervals between the black bars than the postjuv GC (cf. Fig. 470).
Fig. 468. Ad after complete postbr moult, 6 January. Whole wing postbr. Recognizable as ad because the irregularity in the barring near the tip of PC 4 is not repeated on the other PC as would be the case in ly/2y.
Fig. 469. Ad after complete postbr moult, autumn. Whole wing postbr. All blue feathers with narrow black barring. PC 7 shows a disturbance in the barring near the tip which is not repeated on the other PC.
Fig. 470. Ad after complete postbr moult, autumn. Whole wing postbr. Ageing difficult. GC 1 with nine black bars and a faintly visible tenth, thus intermediate between juv and ad. No conspicuous irregularities in barring. However, PC show about the same intervals between black bars as the GC (cf. Fig. 467).
158
FringilLa coelebs
Fringilla coelebs Chaffinch Extent of postjuvenile moult MaC and MeC: all. GC: range 3-10, mean 8.5, mode 9, all GC 14.3% (N=9404). CC: 6.7%. Al: none 95-5%, one 4.3%, two 0.2% (N=6281). T: none 95-4%, one 3.0%, two 1.3%, three 0.3% (N=6276) (see p.
33). R: none 99.2%, one to six 0.8% (N=6263) (see p. 34). S: one 6 renewed S 6 on both wings together with all T and GC, but without CC, Al and R. The extent of postjuv moult is correlated among different feather tracts. CC, Al and T may be renewed when at least six GC are moulted (Fig. 472). There are no differences in the extent of postjuv moult between the sexes. The extent of postjuv moult decreases as the autumn migratory season proceeds. Birds wintering in Switzerland have relatively few renewed GC, while in spring the mean number of new GC is higher again (Fig. 473). In NW Russia, moult of part or all MaC and MeC, two to ten GC, none to two Al and occasionally the CC was recorded (Rymkevich 1990).
Fig, 471. Extent of postjuv moult on the wing and tail in ly/2y Fringilla coelebs.
Extent of postbreeding moult Whole plumage. Exceptionally (<1%), individual Al (Fig. 483) and PC, in one bird S 5 and in another bird P 9 and PC 9 (Fig. 484) remain unmoulted. Some birds migrate when still in the last stages of wingmoult. Such birds, found between the end of September and the beginning of November, have mostly growing body-feathers, S 5—6 and sometimes P 8—9; one bird from 20 October had growing P 8—9, S 3—5 and P 10 and S 6 still unmoulted. Comments on ageing
Fig. 472. Relationships between the number of postjuv GC and the percentage of individuals with renewed CC, Al, T and R in ly/2y Fringilla coelebs which have completed their postjuv moult.
Best criteria: Skull pneumatization until mid-October (p. 206). Most ly/2y recognizable by moult limit within GC. Distinction between ly/2y with all GC moulted and ad by difference in colour between GC and PC. Plumage characters sometimes difficult to apply, especially in 9. ly/2y: 86% have a moult limit within the GC which is conspicuous in d, but more difficult to detect in 9 . In both sexes, juv GC have generally lighter feather centres than postjuv GC. ly/2y with all GC renewed (14%) show a contrast between postjuv GC and juv PC which is generally more distinct than in ad, but some 9 with all GC renewed are difficult to determine (cf. Fig. 481 and 482), ly/2y always have a lighter Al than ad. Especially ly/2y with all GC renewed sometimes have a moult limit within Al or T, or a renewed CC which can be compared with the paler juv PC (Fig. 479 and 480). Since R are rarely moulted, the shape of their tips may be useful for ageing. Usually, juv R, especially R 1-2, are more pointed than in ad and have no dark spot at their tip (see Svensson 1992). However, some ly/2y show ad-type shapes, and abrasion may prohibit application of this criterion in spring. Ad: No moult limit within GC, Al and T. Innermost R usually less pointed than in ly/2y and, especially in S, mostly with a dark spot at the tip.
Fig. 473. Mean number of postjuv GC in the course of the year of ly/2y Fringilla coelebs which have completed the postjuv moult (data from September until the beginning of November grouped in five-day periods).
Fringilla coelebs
159
Fig. 478. l y e ? after partial postjuv moult, 21 September. MaC and MeC postjuv. GC 1 juv, 2-10 postjuv. Rest of wing juv. Juv GC 1 dark brown, not black like the postjuv GC. Moult limit more conspicuous than in 9 (cf. Fig. 477).
Fig. 474. ly in juv plumage, 3 August. Whole wing juv. Note the loosely textured MaC.
Fig. 475. ly 9 after partial postjuv moult, 1 November. MaC and MeC postjuv. GC 1-6+10 juv, 7-9 postjuv. Rest of wing juv. Recognizable as ly by the difference in colour between juv GC 6 and postjuv GC 7.
Fig. 479. ly 6 after partial postjuv moult, 16 September. MaC, MeC, GC and CC postjuv. Al 1 postjuv, 2-3 juv. Rest of wing juv. The renewed Al 1 and CC contrast with the juv Al 2—3 and PC in their darker colour.
Fig. 476. 2y 6 after partial postjuv moult, 7 April. MaC and MeC postjuv. GC 1—2 juv, 3-10 postjuv. Rest of wing juv. Moult limits within GC are distinct even in spring. Fig. 480. ly 9 after partial postjuv moult, 29 September. MaC, MeC, GC and CC postjuv. T 7 juv, 8—9 postjuv. Rest of wing juv. The renewed CC is of the same colour as the GC and darker than the juv PC. T 8—9 darker and fresher than juv T 7.
Fig. 477. ly 9 after partial postjuv moult, 5 September. MaC and MeC postjuv. GC 1 juv, 2-10 postjuv. Rest of wing juv. Juv GC 1 lighter than postjuv GC, but moult limit less conspicuous than in 6.
Fig.481.2y 9 after partial postjuv moult, 30 April. MaC, MeC and GC postjuv. Rest of wing juv. JuvCC,AlundPC browner and more bleached than renewed GC. This colour difference is slightly more distinct than in ad (cf. Fig. 482).
160
Fringilla coelebs Fig. 482. Ad 9 after complete postbr moult, 29 April. Whole wing postbr. Colour difference between GC and CC, Al and PC not as distinct as in 2y (cf. Fig. 481).A1 darker than in 2y.
Fig. 483. Ad 9 after complete postbr moult, 21 October. Whole wing postbr except Al 2. Exceptionally, Al 2 remains unmoulted and is heavily bleached.
Fig. 484. Ad <$ after postbr moult arrested at P 9, 12 October. Exceptionally, P 9 has not been renewed and is more bleached than the other P. The rest of the wing is fresh, CC, Al and especially PC are deep black
Fringilla montifringilla
161
Fringilla montifringilla Brambling Extent of postjuvenile moult MaC and MeC: usually all. ly with few renewed GC may retain some juv MeC. GC: range 0-10, mean 7.5, mode 8, no GC 0,1%, all GC 3.7% (N=1525). CC: 0.4%. Al: none 98.3%, one 1.7% (N=1257). T: none 96.9%, one 1.8%, two 1.2%, three 0.2% (N=1019) (see p. 33). R: none 99.0%, one to six 1.0% (N=1016). The extent of postjuv moult is correlated among GC, CC, Al and T (Fig. 486). CC, Al and T are renewed when at least eight GC are moulted. The extent of postjuv moult of $ (mean 7-56 GC, N=772) is not significantly different from that of 9 (mean 7.41 GC, N=749). The extent of postjuv moult decreases as the autumn migratory season proceeds and reaches a minimum in winter (Fig. 487). In NW Russia, Rymkevich (1990) recorded moult of MaC, MeC, GC, CC and Al, but not of T. cT moult on average 7.2 GC (range 4-10, all GC 0.8%, N=276), 9 on average 7.3 GC (range 4-10, all GC 0.5%> N=279; difference between sexes not significant) and thus renew slightly fewer GC than migrants and wintering birds observed in Switzerland. Extent of postbreeding moult Whole plumage (Ottosson & Haas 1991). Exceptionally, S 6 and/or one or two Al (Fig. 495) remain unmoulted. Fig. 486. Relationships between the number of postjuv GC and the percentage of individuals with renewed CC, Al, T and Rin \y/2yFringilla montijringilla which have completed their postjuv moult.
Fig. 487. Mean number of postjuv GC during autumn and winter of ly/2y Fringilla montifringilla which have completed the postjuv moult (data grouped in five-day periods; the first value includes the period 28 September-7 October; winter includes the period 23 Decemberâ&#x20AC;&#x201D;9 Februarv).
Fig. 485- Extent of postjuv moult on the wing and tail in ly/2y Fringilla montifringilla.
Comments on ageing Best criteria: Skull pneumatization until the end of October (p. 206). Most ly/2y recognizable by moult limit within GC. Distinction between ly/2y with all GC moulted and ad, by difference in colour between GC and PC. Plumage characteristics sometimes difficult to apply, especially in 9. ly/2y: 96% have a moult limit within the GC which is distinct in c? (Fig. 490 and 491), but more difficult to see in 9, especially when within the outer GC (Fig. 492). In both sexes, juv GC have lighter feather centres than renewed GC; central and inner juv GC have a whitish, not rust-brown tip (Fig. 489). ly/2y with all GC moulted (4%) show a stronger contrast between postjuv GC and juv PC, Al and CC than ad (Fig. 493), but this may be difficult to judge in 9 . Moult limits within Al (Fig. 491) and T (Fig. 492) are rare. As an additional criterion, the shape of R may be used, although some ly/2y show almost ad-type shapes, and abrasion may prohibit the evaluation of the shape in winter and spring. Especially the inner R are usually more pointed than in ad. Rarely ly/2y show a moult limit within R where pointed and more rounded R meet. Most ly S have some black spots on MaC (Fig. 490 and 491). <S during the breeding season which have dull black head feathers with large brown fringes are 2y, those with small brown fringes may be ad or 2y (Hogstad & Roskaft 1987). Ad: No moult limit within GC, Al, T and R. R usually more rounded than in ly/2y. Most ad <S have no black spots on MaC (Fig. 494). <J during the breeding season with glossy black heads often tinged bluish are ad (Hogstad & Roskaft 1987). Fig. 488. ly 9 after partial postjuv moult, 13 October. Two inner MaC juv, rest posrjuv. MeC 1 juv, 2-8 postjuv. GC 1â&#x20AC;&#x201D;5 juv, 6-10 postjuv. Rest of wing juv. Juv MaC recognizable by their light fringes and looser structure. Juv MeC 1 with white, not rusty tip. In 9 , however, inner postjuv MeC usually show lighter tips as well (cf. Fig. 492,493 and 495). Distinct contrast between juv and postjuv GC,
162
Fringilla montifringilla Fig. 489. ly 9 after partial postjuv moult, 21 October. MaC and MeC postjuv. GC l-5+10juv,6-9 postjuv. Rest of wing juv. The juv GC contrast with the moulted GC in their dark brown, not black feather centres and their whitish, not rusty tips.
Fig. 493. ly 9 after partial postjuv moult, 10 October. MaC and MeC postjuv. GC postjuv. Rest of wing juv. Contrast between postjuv GC and juv PC, CC and Al slightly more marked than in ad (cf. Fig. 495).
Fig. 490. ly 6 after partial postjuv moult, 6 October. MaC and MeC postjuv. GC 1-2 juv, 3-10 postjuv. Rest of wing juv. JuvGC 1-2 with lighter Feather centres than renewed GC and with whitish not rustybrown tips.
Fig. 491. ly <? after partial postjuv moult, 11 October. MaC and MeC postjuv. GC 1 juv, 2-10postjuv.Al 1 postjuv, 2-3 juv. Rest of wing juv. The renewed Al 1 is jet black like the renewed GC.
Fig. 492. ly 9 after partial postjuv moult, 11 October. MaC and MeC posrjuv. GC 1 juv, 2-10 postjuv. T 7 juv, 8-9 postjuv. Rest of wing juv. In r , the feather centre of juv GC 1 is only slightly lighter than those of renewed GC. The postjuv T 8-9 are slightly darker than the juv T 7.
Fig. 494. Ad 3 after complete postbr moult, 6 October. Whole wing postbr. Dark parts of the wing including PC and Al jet black.
Fig. 495. Ad 9 after complete postbr moult, 25 October. Whole wing postbr except Al 2. Contrast between GC and PC, CC and Al less marked than in ly/2y (cf.Fig.493).A12 remains unmoulted.
Serinus serinus
163
Serinus serinus Serin Extent of postjuvenile moult MaC and MeC: usually all. ly with no or few moulted GC may retain some or all juv MeC and some juv MaC. GC: range 0-10, mean 6.5, mode 7, no GC 3.3%, all GC 10.1% (N=1019). CC: 21.6%. Al: none 84.8%, one 14.7%, two 0.5% (N=972). T: none 71.9%, one 4.5%, two 15.1%, three 8.4% (N=991) (see p. 33). R: none 84.0%, one 12.1% (mostly R 1), two to six 3.9% (N=989) (see p. 34). S and P: if all GC and T are moulted, sometimes S 6 is also renewed (Fig. 506). We found four birds with eccentric P-moult: one 2y (Ventotene, Italy) with P 5-10, PC 1-4, CC, Al 1-2, T and Rpostjuv, rest juv; three ly (Col de Bretolet, Switzerland) with P 6 renewed on one side (two birds) or P 5 renewed on one side (one bird); all three had also moulted all GC, CC and various Al, T and R. The extent of postjuv moult is correlated among GC, CC, Al, T and R (Fig. 497). CC and T may be moulted when at least five GC are renewed, Al 1 when at least four GC renewed and some R when at least three GC renewed. The extent of postjuv moult in S (mean GC 6.7, T 0.6, R 0.25, N=421) is not significantly different from that in $ (mean GC 6.4, T 0.6, R 0.22, N=540). The extent of postjuv moult decreases as the autumn migratory season proceeds (Fig. 498). In Portugal, eccentric P-moult, and in some birds complete postjuv moult, was found (Ginn & Melville 1983, Harris 1992) and this may be true for other southern populations as well. However, complete postjuv moult was never seen in birds examined on the Balearic Islands (Mester&Pruntel982).
Fig. 497. Relationships between the number of postjuv GC and the percentage of individuals with renewed CC, Al, T and R i n ly 12y Serinus serinus which have completed their postjuv moult.
Fig. 498. Mean number of postj-uv GC during autumn of ly Serinus serinus which have completed the postjuv moult (data grouped in five-day periods; the first value includes the period 18 September-2 October, the last 28 Octobet-6 November).
Fig. 496. Extent of postjuv moult on the wing and tail in ly/2y Serinus serinus.
Extent of postbreeding moult Whole plumage. Some birds migrate when still in the last stages of wing-moult, having P 9 and/or S 5-6 still growing up to the end of October. Comments on ageing Best criteria: Skull pneumatization up to at least end of October (p. 206). Most ly/2y recognizable by moult limit within GC. Also check for moult limits within MeC, Al, T and R and the difference in colour between GC and PC, especially to distinguish ly/2y with all GC moulted from ad. ly/2y: 87% show a moult limit within the GC which is easily recognized. Juv GC have lighter tips, lighter feather centres and less greenish outer fringes. The colour of the feather centres is decisive especially in 2y with worn and bleached fringes (Fig. 503 and 505). ly/2y with no GC renewed (3%) usually retain some juv MeC or juv MaC which are easily recognized by their whitish fringes (Fig. 500). ly/2y with all GC moulted (10%) usually have renewed CC and Al 1 (Fig. 497) with darker feather centres and more greenish fringes than the juv Al 2-3 and the PC (Fig. 506 and 507). In addition, such birds can be recognized by moult limits within T, between T and S and within R. Juv R are more pointed than renewed R (see also Rohner 1981). Ad: No moult limits within GC, Al, T, R and between S and T. No difference in colour between CC, Al and PC.
Fig. 499. ly at the beginning of partial postjuv moult, 9 August. Innermost MaC already partially postjuv, rest of wing juv. All GC and MeC fringed whitish.
164
Serinus serin us
Fig. 500. ly 6 after partial postjuv moult, 22 October. Outermost MaC juv, rest postjuv. MeC 2 juv, 1+3-8 postjuv. GC 1-8+10 juv, 9 postjuv. Rest of wingjuv. Renewed GC 9 intact and fringed brown, juv MeC 2 fringed whitish.
Fig. 501. ly 9 after partial postjuv moult, 16 October. MaC and MeC postjuv. GC 1-7 juv, 8-10 postjuv. Rest of wing juv. Juv GC tipped whitish, shorter and more worn than postjuv GC which have darker tips. In 9, postjuv MeC may have light fringes.
Fig. 502. ly $ after partial postjuv moult, 16 October. MaC and MeC postjuv. GC 1-4 juv, 5—10 postjuv. Rest of wing juv. Juv GC with lighter fringes and feather centres than renewed GC.
Fig. 503. 2y $ after partial postjuv moult, 29 April. MaC and MeC postjuv. GC 1—3 juv, 4-10 postjuv. Rest of wing juv. Tips of juv and postjuv GC markedly worn and bleached. In spring, juv GC are recognizable mainly by their browner feather centres.
Fig. 504. ly cT after partial postjuv moult, 2 October. MaC and MeC postjuv. GC 1-2 juv, 3-10 postjuv. T 7 juv, 8-9 postjuv. Rest of wing juv. The moult limit within GC, as well as the moult limit within T is diagnostic ofly.
Fig. 505. 2y cT after partial postjuv moult, 29 April. MaC and MeC postjuv. GC 1 juv, 2—10 postjuv. CC postjuv. T 7 juv, 8—9 postjuv. Rest of wing juv. Juv GC 1 with browner feather centre than renewed GC and with whitish, not greenish fringe. Renewed CC fringed greenish, not brownish.
Fig. 506. ly 6 after partial postjuv moult, 11 October. MaC, MeC and GC postjuv. CC and Al 1 postjuv. T and S 6 postjuv. Rest of wing juv. Distinct moult limit between the lighter S 1—5 and the renewed and darker S 6 and T 7-9. Postjuv CC and Al 1 distinguished from juv Al 2-3 and PC by their green fringes.
Serinus serinus Fig. 507. 2y 9 after partial postjuv moult, 1 May. MaC, MeC and GC postjuv. CC and Al 1 postjuv. T 7 juv, 8-9 postjuv. Rest of wing juv. Recognizable as 2y mainly by the renewed CC and Al 1, which contrast with the juv Al 2-3 and PC in their darker feather centres and green fringes.
Fig. 509. Ad d after complete postbr moult, 4 May. Whole wing postbr. No moult limits.
Fig. 508. Ad 9 after complete postbr moult, 18 October. Whole wing postbr. No moult limits within GC and between S and T. CC and Al 1 have the same colour of feather centre and fringe as Al 2-3 and PC.
165
166
Serinus chrinella
Serinus citrinella Citril Finch Extent of postjuvenile moult MaC and MeC: usually all. ly with few moulted GC may retain some outer juv MeC, ly with no moulted GC even all juv MeC and some MaC. GC: range 0-10, mean 6.6, mode 7, no GC 0.2%, all GC 1.3% (N= 863). CC: 2.2%. Al: none 99.4%, one 0.6% (N=788). T: none 93-1%, one 3.9%, two 1.7%, three 1.2% (N-813) (see p. 33). R: none 97.8%, one 1.6%, two 0.1%, three 0.2%, six 0.2% (N=813). The extent of postjuv moult is correlated among GC, CC, Al, T and R (Fig. 511). R may be renewed when at least five GC are moulted, T when at least four GC, CC when at least seven GC and Al 1 when at least six GC are moulted. $ moult significantly more GC (mean 7.1, N=400) than $ (mean 6.2, N=410). For T and R, there are no significant differences between the sexes. In both sexes, the extent of postjuv moult decreases as the autumn migratory season proceeds (Fig. 512). In Bavaria, three to eight GC are moulted (mean 6.2, mode 7, N=105; Brandl & Bezzel 1989) which corresponds approximately with our data. Extent of postbreeding moult Whole plumage. Exceptionally, (< 1%) individual PC, S 1 (Fig. 521) or S 6 remain unmoulted. Wing-moult often extends into October. Even at the end of October, migrating birds may still show growing P 9 and S 5-6.
Fig. 511. Relationships between the number of postjuv GC and the percentage of individuals with renewed CC, Al, T and R i n ly/2y Serinus citrinella which have completed their postjuv moult.
Fig. 512. Mean number of postjuv GC during autumn of S (dots) and 9 (triangles) ly Serinus citrinella which have completed the postjuv moult (data grouped in five-day periods; the first pair of values includes the period 3â&#x20AC;&#x201D;17 September, the last28October-6 November).
Fig. 510. Extent of postjuv moult on the wing and tail in ly/2y Serinus citrinella.
Comments on ageing Best criteria: Skull pneumatization until at least mid-November (p. 206). Moult limits within GC, Al, T and R, ly/2y: 98% have a moult limit within GC which is conspicuous until the first postbr moult (starting mid-July of the second year). The fringes of moulted GC are green or greenish-yellow, those of juv GC are white or off-white. In both sexes, moult limits within GC are easily recognized although postjuv GC have less intensely coloured fringes in 9 (Fig. 516) than in 6 (Fig. 518). ly/2y with all GC moulted (Fig. 519) are more difficult to determine, but usually have a moult limit within Al or between CC, GC and PC. The greenish fringe of Al 2, which is never moulted, is narrow in ly/2y, but larger and more conspicuous in ad (cf. Fig. 519 and 520). The outer edges of S are pale greenish in ly/2y and bright green in ad. About half of the ly/2y with all GC moulted have moult limits within T (Fig. 517) and R. Juv R are more pointed than postjuv. Ad: No moult limit within GC, Al, T and R. T and S with bright green outer edge. Al, especially Al 2, usually with broad bright green outer edge. Also check for growing S 5-6 well into October.
Fig. 513. ly in juv plumage, 1 August. Whole wing juv. MeC and GC broadly fringed off-white.
Serinus citrine/la Fig. 514. ly after partial postjuv moult, 25 October. MaC mostly postjuv, some juv MaC above MeC. MeC, GC and rest of wing juv. ly with a postjuv moult of exceptionally limited
Fig. 515. ly 9 after partial postjuv moult, 16 October. MaC postjuv. MeC 1 juv, 2-8 postjuv. GC 1-7+10 juv, 8-9 postjuv. Rest of wing juv. Renewed GC with green, juv GC with white fringes.
Fig. 516. ly 9 after partial postjuv moult, 13 October. MaC and MeC postjuv. GC 1-5+10 juv, 6-9 postjuv. Rest of wing juv. The moult limit within GC is easily visible even when the fringes of postjuv GC are less intensely green, as is often the case in 9.
Fig. 517, ly 6 after partial postjuv moult, 13 October. MaC and MeC postjuv. GC 1 juv, 2-10 postjuv. CC postjuv. T 8 postjuv, 7+9 juv. Rest of wing juv. Renewed T 8 and CC with green outer edge and dark feather centres like postjuv GC.
167
Fig. 518. ly d after partial postjuv moult, 1 October. MaC and MeC postjuv. GC 1-3 juv, 4-10 postjuv. Rest of wing juv. Conspicuous moult limit within GC. Fringes of renewed GC bright yellow-green.
Fig. 519. ly <J after partial postjuv moult, 17 October. MaC, MeC and GC postjuv. CC postjuv. Rest of wing juv. Juv Al 2 without green outer edge and with lighter feather centre than postjuv GC and CC.
Fig. 520. Ad cT after complete postbr moult, 5 October. Whole wing postbr. Al 1-2 with conspicuous green fringes and dark feather centres, like CC and PC.
Fig. 521. Ad 9 after complete postbr moult, 18 October. PC 8 and S 1 unmoulted, rest of wing postbr. Exceptionally, S 1 and PC 8 remained unmoulted during the complete postbr moult.
168
Carduelis chloris
Carduelis chloris Greenfinch Extent of postjuvenile moult MaC and MeC: all. GC: range 1-10, mean 9.3, mode 10, all GC 71.6% (N=264). CC: 65.5%. Al: none 39.3%, one 37.2%, two 9.7%, three 13-8% (N=247). T: none 42.6%, one 9.6% two 20.9%, three 26.9% (N=249) (see p.
33). R: none 53.3%, one 16.8%, two 4.5%, three 1.6%, four 3.3%, five 0.8%, six 19.7% (N=244) (see p. 34). S: one bird had S 5—6 (Fig. 533) and two birds S 6 moulted, all three also had eccentrically renewed P (N=217). P: In Switzerland, 10% (N=217) underwent eccentric P-moult, Most of these birds renewed one to three P among P 5—7; the maximum extent was recorded in two birds with P 5—10 and in two birds with P 4—10 moulted. PC were not moulted or not necessarily together with the corresponding P. In Italy (Ventotene Island), 28% of spring migrants (N=43) showed one to four eccentrically renewed P. One bird moulted P 2-7+9 on one wing and P 1-3+8 on the other. The extent of postjuv moult is correlated among different feather tracts (Fig. 523). Most birds with new CC, Al, T or R have all GC renewed. .All birds with eccentric P-moult had all GC and CC renewed, most of them all Al, T and R. cT moult on average slightly more GC, T and R than 9, but the differences are not significant. In Switzerland, the extent of postjuv moult is least during winter (Fig. 524). In Finland, slightly fewer R are moulted than in Switzerland: 15% (19.7% in Switzerland) of ly renewed all R, 22.9% (27.0% in Switzerland) one to five R (Lehikoinen & Laaksonen 1977). In central and W Europe, the percentage of ly with all GC moulted varies some-
Fig. 523. Relationships between the number of postjuv GC and the percentage of individuals with renewed CC, Al, T and R in ly/2y Carduelis chloris which have completed their postjuv moult.
Fig. 522. Extent of postjuv moult on the wing and tail in ly/2y Carduelis chloris.
what and is lower than that recorded in Switzerland (71.6%): Germany 58.6% (Prill in Blumel 1976), 31.6% (Westphal 1976) and 44% (Drost 1931); England 44-55% (M.Boddy in Ginn & Melville 1983). In NW Russia, postjuv moult generally includes all MaC and MeC, two to ten GC, sometimes the CC and none to all T, Al and R (Rymkevichl990). The Greenfinch is amongst those species which regularly renew P eccentrically (see p. 36), and is the first central European species for which eccentric P-moult was described in detail (Westphal 1976). In Berlin, 16 out of 133 (12%) ly showed P-moult: one bird had all P and S, but not all PC renewed, three more were at the beginning of a regular descendant P-moult, the others had one to four eccentrically renewed P (Westphal 1976). One 2y bird from Ibiza was also recorded with eccentrically renewed P 5—6 and new GC, Al, CC and R (Mester & Priinte 1982). In NW Russia, eccentric moult of P 5 or P 6 (rarely P 3-7) was recorded in early-hatched ly, but not renewal of S (Rymkevich 1990). Complete P-moult, as recorded in Berlin (Westphal 1976), England (1%) and Portugal (10-20%) (Ginn & Melville 1983, Harris 1992), was not recorded in Switzerland. Busse (1984) suggests that about 15% of central European ly Greenfinches may perform a complete moult, but we consider this value too high without more supporting data. Extent of postbreeding moult Whole plumage. Comments on ageing Best criteria: Skull pneumatization until mid-October (p. 206). Since ly born early in the season are more likely to have both an extensive postjuv moult and an early completion of skull pneumatization, ageing after mid-October often has to rely on plumage characters which are difficult to apply: slight differences in colour and wear among T, beween T and S, among Al, between GC, CC, Al and PC, among R or among P. ly/2y with fully pneumatized skull and complete postjuv moult are inseparable from ad.
Fig. 524. Mean number of postjuv GC in the course of the year of 1 y/2y Carduelis chloris which have completed the postjuv moult.
ly/2y: 28% show a moult limit within GC which is easily recognized. Juv GC have a lighter tip, a stronger contrast between fringe and feather centre, more brownish feather centres and are often shorter than renewed GC (Fig. 526 and 527). Most ly/2y have all GC renewed and can be aged only with experience. Most helpful is a moult limit within T (42% of those with all GC renewed) which can be recognized by differences in wear (Fig. 529) or in the colour of the tip and outer web (Fig. 530). Birds with all T moulted (38% of those with all GC renewed) can often be recognized by differences in wear and colour
Carduelis chloris
of the feather centres and the outer fringes between T and juv S (Fig. 532). Birds with no renewed T (20% of those with all GC renewed) are difficult to determine (Fig. 528). Thus, checking for moult limits in the area of CC, Al and PC is always necessary. Renewed CC and Al are brighter than juv and contrast with the more brownish and less bright juv PC (Fig. 531). A renewed Al 1 has the same green or yellow colour as the adjacent MaC which are always moulted (cf. Fig. 529 with Fig. 530). Moult limits within R may be another useful criterion and are usually, but not always, conspicuous. Unmoulted R are usually more pointed and have lighter feather centres (especially in cT) than renewed R. R without a moult limit are difficult to judge. Furthermore, check all birds for renewed P (Fig. 532 and 533). All these criteria are more conspicuous in cT than in 9 .
169
Fig. 527. 2y 9 after partial postjuv moult, 3 May. MaC and MeC postjuv. GC 1—2 juv, 3-10 postjuv. Rest of wing juv. Conspicuous moult limit within GC. Juv GC with lighter fringes and tips and browner feather centres.
Ad: Whole plumage without moult limits. With experience, ad 6 may be recognized by their brightly coloured PC although some individual variation exists. Juv PC are usually browner, and in most cases have only a slight yellowish-green edge and no grey terminal fringe (cf Fig. 533 and 534). In 9, these differences are less conspicuous.
Fig. 528. ly 9 after partial postjuv moult, 17 October. MaC, MeC and GC postjuv. CC and Al 1 postjuv. Rest of wing juv. Recognizable as ly by the brightly coloured postjuv CC and Al 1, which contrast with the more brownish Al 2—3 and PC.
Fig. 525. ly (5 at the beginning of partial postjuv moult, 31 July. Some inner MaC postjuv, rest of wing juv. Juv MaC and MeC looser than renewed MaC.
Fig. 526. ly 9 after partial postjuv moult, 13 October. MaC and MeC postjuv. GC 1-7+10 juv, 8-9 postjuv. Rest of wing juv. Rare case of a limited extent of postjuv moult. The two renewed GC are longer and darker.
Fig. 529. 2y <S after partial postjuv moult, 9 May. MaC, MeC and GC postjuv. CC postjuv, Al 1 postjuv, 2—3 juv. T 8 postjuv, 7+9 juv. Rest of wing juv. Recognizable as 2y by the moult limit within T and Al. The renewed T 8 is less worn and has a greyer outer web than T 7+9.
170
Carduelis chloris
Fig. 530. ly cT after partial postjuv moult, 23 October. MaC, MeC and GC postjuv. CC postjuv. T 7 juv, 8—9 postjuv. Rest of wing juv. Recognizable as ly by the moult limit within T.
Fig. 533. 2y c5 after eccentric partial postjuv moult, 10 May. MaC, MeC and GC postjuv. CC and Al 1-3 postjuv. T and S 5—6 postjuv. P 5—6 postjuv. PC and rest of wing juv. The eccentrically renewed P 5-6 are slightly darker and have more intensely coloured yellow outer webs than the other P. The renewed S 5—6 have darker feather centres and a more intensely coloured grey outer fringe than the juv S.
Fig. 531. ly 9 after partial postjuv moult, 17 October. MaC, MeC and GC postjuv. CC and Al 1-3 postjuv. T postjuv. Rest of wing juv. The renewed CC and Al 1—3 contrast with the brownish juv PC in their darker feather centres and brighter colour.
Fig. 534. Ad 6 after complete postbr moult, 23 October. Whole wing postbr. No moult limits. PC intensely coloured.
Fig. 532. ly 9 after eccentric partial postjuv rnoult, 22 October. MaC, MeC and GC postjuv. CC and Al 1-3 postjuv. T postjuv. P 7 postjuv. PC and rest otwing juv. The eccentrically renewed P T is darker than the adjacent P. The moult limit between T 7" and S 6 is inconspicuous. The postjuv T are slightly fresher and have darker feather centres than juv S 1-6.
Fig. 535. Ad 9 after complete postbr moult, 31 October. Whole wing postbr. No moult limits. Especially in 9 , ad are difficult to distinguish from ly/2y with an extensive postjuv moult (cf. Fig. 531 and 532).
Carduelis carduelh
171
Carduelis carduelis Goldfinch Extent of postjuvenile moult MaC and MeC: usually all. ly with few moulted GC may retain some juv MeC. GC: range 2-10, mean 8.9, mode 10, all GC 40.8% (N=473). CC: 1.4%. Al: none 98.1%, one 1.6%, two 0.2% (N=431). T: none 17.0%, one 20.0%, two 15.7%, three 47.3% (N=465) (see p. 33). R: none 54.0%, one 14.1%, two 20.4%, three 6.3%, four 3.0%, five 0.9%, six 1.3% (N=461) (see p. 34). P and S: Seven ly with eccentrically moulted P are known from Switzerland. Three of them renewed P 6, one P 5, one P 3-6, one P 4—6 and one P 5—7. All seven birds moulted all GC, T and all or some R, one bird also S 6. No renewed PC were recorded. In addition to these birds, one ly from September started a regular descendant Pmoult (P 1-4 new, 5-6 growing, 7-10 old, S old, T 7 old, 8-9 growing, R 1 growing, 2—6 old, GC new). In this individual, it is not known whether or not it finished P- and S-moult. The extent of postjuv moult is correlated among GC, CC, Al, T and R (Fig. 537). T and R may be renewed when at least seven GC are moulted, Al 1 when at least eight, and CC when all GC are moulted. 9 (N=198) moult significantly fewer GC (mean 8.7), T (1.7) and R (0.7) than 6 (means GC 9.3, T 2.3, R 1.3, N=190). In both sexes, the extent of postjuv moult decreases as the autumn migratory season proceeds (Fig. 538). The extent of postjuv moult varies with geographical area. In NW Russian birds, early-hatched ly moult all GC and occasionally some T and Al, late-hatched usually only four GC; moult of P, S, PC, CC and R was not observed (Rymkevich 1990). Scandinavian birds only rarely
Fig. 537. Relationships between the number of postjuv GC and the percentage of individuals with renewed CC, Al, T and R in ly/2y Carduelis carduelis which have completed their postjuv moult.
Fig, 536. Extent of postjuv moult on the wing and tail in ly/2y Carduelis carduelis.
moult all GC (Svensson 1992). In central, and even more so, in S Europe, the majority of ly moult all GC. In central Europe, eccentric and the initial stages of regular P-moult are rare; in S Europe they are frequent. The most detailed data available are from the Balearic Islands (Mester & Priinte 1982) where two thirds of ly moult one to eight P, sometimes also S (N=l 17, see also p. 36). Complete moult of all P and S, however, was not recorded. In Greece, four or five outer P are frequently renewed (Kasparek 1981). Near Rome, two ly were found starting a regular P-moult (Fraticelli & Gustin 1987b). ly with a complete moult are mentioned from Sicily, S Spain and S Portugal (Newton 1968a, Harris 1992). According to Ginn & Melville (1983), 3^% of British ly perform a complete moult. Some ly, especially in S Europe, may indeed perform a complete moult and can be recognized only by skull pneumatization during the first few months after fledging. However, it is advisable not to take every ly starting P-moult as evidence for a complete moult; Mester & Prunte (1982) found that ly never moulted P9 and some central S on the Balearic Islands and, hence, interrupt their regular P-moult. Extent of postbreeding moult Whole plumage. Ad with still growing P 9 and S 6 occur regularly during autumn migration, until the end of October. One ad from 2 November with almost full-grown P 9 and S 4, but old P 10 and S 5-6 suggests that moult interruption may sometimes occur. Comments on ageing Best criteria: Skull pneumatization until at least November (p. 206). Moult limits within GC, T, R, between T and S and between GC, CC, Al and PC. ly/2y after a complete moult and with a fully pneumatized skull are inseparable from ad.
Fig. 538. Mean number of postjuv GC during autumn of 6 (dots) and 9 (triangles) ly Carduelis carduelis which have completed the postjuv moult (data grouped in five-day periods; the first pair of values includes the period 13—27 September, the last 23 October-6 November).
ly/2y: In order to identify juv and postjuv GC it is important to realize that the extent of yellow on postjuv GC varies between individuals. Usually, the yellow area increases from GC 3 to GC 8. Both juv and postjuv GC 10 are only black and buff. Postjuv GC 9 may be similar to GC 10 (Fig. 540) or may show some yellow. Juv GC 1-2 have buffish terminal fringes (in spring bleaching to white, Fig. 542); postjuv GC 1 white, postjuv GC 2 white or yellow terminal fringes. Moult limits within inner and central GC are easily recognizable by differences in the brightness of the yellow area (Fig. 540). Moult limits within GC 1-3 (over 50% of ly/2y) can be recognized by differences in the intensity of the black between juv and postjuv GC (Fig. 541-543). Birds with all GC renewed (41%) are more difficult to age; the renewed GC have a more intensive, often glossy black colour than the duller juv CC, Al and PC (cf. Fig. 544 and 547). Always check for
Carditelis cnrduelis
moult limits within T or between T and S (83% of ly/2y). Juv T and S are duller black than postjuv (Fig. 543, 545, 546). Often moult limits within R are helpful (45%). Juv R are more pointed and more worn than postjuv. However, some ly moult all R. Eccentrically moulted P (mostly P 5 and/or 6) are to be expected only when all GC are renewed. Their outer webs are brighter yellow (Fig. 545) and, especially in spring when the yellow is bleached, their tips are less worn than in the adjacent juv P (Fig. 546).
Fig. 542. 2y 9 after partial postjuv moult, 19 April. MaC and MeC postjuv. GC 1-2 juv, 3-10 postjuv. T 8 postjuv. Rest of wing juv. Juv GC 1-2 less deeply black than the adjacent postjuv GC.
Ad: GC, PC, CC and Al of the same deep black colour. No moult limits within GC, R, T or between T and S (Fig. 547).
Fig. 539. ly in juv plumage, 13 August. Whole wing juv. MeC with broad huffish fringes, central GC pale yellow.
Fig. 540. ly 9 after partial postjuv moult, 19 October. MaC almost all postjuv. MeC 4 postjuv, the others juv. GC 1-6+10 juv, 7—9 postjuv. Rest of wing juv. Conspicuous moult limit between the juv yellowish-white GC 6 and the renewed yellow GC 7. The postjuv MeC 4 is completely black and contrasts with the paler juv MeC.
Fig. 543. ly 9 after partial postjuv moult, 25 September. MaC and MeC postjuv. GC 1 juv, 2—10 postjuv. T 7—9 postjuv. Rest of wing juv. Juv GC 1 less deeply black than the adjacent postjuv GC and with a buffish terminal fringe. Slight difference in colour between renewed T 7 and juv S 6.
Fig. 544. ly R a f t e r partial postjuv moult, 31 October. MaC, MeC and GC postjuv. AJ 1 postjuv, 2—3 juv. T 7-9 postjuv. Rest of wing juv. The renewed GC 1-10 and Al 1 are slightly darker black than the juv CC, Al 2-3 and PC.
Fig. 541. ly 9 after partial postjuv moult, 31 October. MaC and MeC postjuv. GC 1-3 juv, 4—10 postjuv. Rest of wing juv. Juv GC dull black, with large buffish fringes already worn. Fig. 545. ly after eccentric partial postjuv moult, 18 September. MaC, MeC and GC postjuv. T 7 growing , 8-9 postjuv. P 6 postjuv. Rest of wing juv. The eccentrically moulted P 6 has a brighter yellow outer web and a less worn tip than the adjacent juv P.
Carduelis carduelis
Fig. 546. 2y 6 after eccentric partial postjuv moult, 28 April. MaC, MeC and GC postjuv. T postjuv. P 6 postjuv. Rest of wing juv. Juv P more worn than renewed P 6. Outer web of T 7 slightly more glossy black than in juv S 6.
173
Fig. 547. Ad <S after complete postbr moult, 2 May. Whole wing postbr. No differences in colour and gloss between T and S. CC, Al and PC of the same deep black colour as GC.
Carduelis spinus Siskin Extent of postjuvenile moult MaC and MeC: usually all. ly with few or no moulted GC may retain some juv MeC and rarely some MaC. Most ly with no GC moulted retain also some juv body-feathers, especially on the head. Exceptionally, single MeC may be retained even when all GC are moulted. GC: range 0-10, mean 7.2, mode 8, no GC 0.6%, all GC 11.9% (N=6786). CC: 6.8%. Al: none 95.9%, one 3.2%, two 0.7%, three 0.2% (N=5735), T: none 74.3%, one 5-2%, two 13-8%, three 6.7% (N=6689) (see p. 33). R: none 82.1%, one 6.9%, two 3.1%, three 1.0%, four 0.4%, five 0.8%, six 5.7% (N=6649) (see p. 34). S: In the course of an extensive postjuv moult, a few ly (0.5%) replace some S. 44% of them also moult some P. Most of them (70%) renew S 6 or S 5-6 along with all T (Fig. 560). Less frequently, individual S out of S 1â&#x20AC;&#x201D;4 are moulted, sometimes together with S 6 (Fig. 561). It remains uncertain whether such S have been replaced accidentally or during a regular moult. P and PC: A small (77 ly out of 5926, 1.3%) and annually varying percentage (between 0.1 and 5-7%) perform a partial P-moult, mostly eccentrically (p. 36). 80% of them renew all GC, one to three T and R and at least one Al or CC. Thus, eccentric P-moult in the Siskin is not necessarily linked to a complete GC-moult. In 55% of the cases, eccentric P-moult comprises only one P (mostly P 6 or P 5, frequently on one wing only), in 37% two to three P (usually P 5-6 or P 5-7, Fig. 558 and 559) and in 8% four to eight P (in four birds two separate blocks of P, e.g. P 1-2+5-7, Fig. 560; maximum extent P 3-10 renewed). The corresponding PC are usually not moulted. A few birds
Fig. 548. Extent of postjuv moult on the wing and tail in ly/2y Carduelis spinus. P see text.
with an apparently descendant P-moult, starting with P 1, are known: two birds with P 1-6, one bird with P 1-7 and two birds with P 1-8 moulted (Fig. 561), together with all GC, CC, T, R, up to four S, at least two Al and irregularly some PC. These birds suggest that complete postjuv moult may also occur, although no conclusive record is known. The extent of postjuv moult is correlated among GC, CC, Al, T and R. R and CC may be renewed when at least five GC are moulted, T when at least six and Al when at least seven GC are moulted (Fig. 549). The postjuv moult is significantly more extensive in $ than in $ : $ moult on average 7.4 GC, 0.57 T, 0.62 R, 9.0% of them the CC and 5.3% one to three Al; 9 moult on average 6.9 GC, 0.47 T, 0.46 R, 4.4% of them the CC and 3.0% one to three Al. In both sexes, the extent of postjuv moult decreases as the autumn migratory season proceeds and reaches a minimum in winter and spring (Fig. 550). The postjuv moult described here is apparently more extensive than that reported from Scandinavian, NW Russian and British birds (Ginn & Melville 1983, Cooper & Burton 1988, Rymkevich 1990, Martin
174
Carduelis spinus
Fig. 549- Relationships between the number of postjuv GC and the percentage of individuals with renewed CC, Al, T and Rin ly/2y Carduelis spinus which have completed their postjuv moult. Fig. 550. Mean number of postjuv GC in the course of the year of 6 (dots) and 9 (triangles) ly/2y Carduelis spinus which have completed the postjuv moult (from September until the beginning of November, data grouped in five-day periods).
1992, Svensson 1992) and possibly concerns mainly central European birds. However, Sellers (1986) in Great Britain found on average 3.1 unmoulted GC (range 1-6, N=104), similar to our data, but no difference between the sexes, and Senar &C Copete (1992) a similar number of renewed T (one T by 6.2%, two by 11.9%, three by 1.3%, N=1877). In NW Russia (Rymkevich 1990), most birds renew all body-feathers, MaC and tail-coverts, usually MeC and some GC (mean 5.1, range 0-10, mode 4, no GC 4.6%, all GC 2.3%, N-772; significantly different from the data from Switzerland), rarely CC, Al, T and R. Moult of S, P and PC was not recorded. Some NW Russian birds from very late broods may moult only MaC, tail-coverts and part of the body-feathers or they may virtually retain the juv plumage. According to Rymkevich (1990), autumn migration may start at any stage of postjuv moult.
wear (Fig. 553). ly/2y with no renewed GC (0.6%) are easily identified by moult limits within MeC or between MeC and MaC (Fig. 552). ly/2y with all GC moulted (12%) are more difficult to determine. In 45% of these birds, moult limits within T and R exist. Juv T have a yellowish-white, postjuv T a greenish-yellow fringe, this difference being more pronounced in 6 than in 9 (cf. Fig. 555 and 556). Juv R are more worn and usually more pointed than postjuv R. ly/2y with all GC, T and R moulted are difficult to distinguish from ad (Fig. 557). In these cases, check for moult limits within Al (Fig. 558), for renewed S (Fig. 560 and 561) and for eccentrically moulted P. Renewed P have more intensely yellow coloured outer webs than juv P (Fig. 558-560). The criterion given by Cooper & Burton (1988) concerning the difference in shape and coloration between juv and postjuv/postbr T 8 is misleading when ly/2y have renewed T 8 (cf. Martin 1992, Senar & Copete 1992).
Extent of postbreeding moult
Ad: No moult limits within the feathers of the wing and tail, except if moult is interrupted. Such birds are easily identified as ad by their retained worn and bleached feathers (Fig. 562).
Usually whole plumage. Ad Siskins may interrupt the postbr moult more frequently than other finches (55 out of 2158 ad, 2.5%, though varying annually from 0% to 4.0%). In 63% of the ad with an interrupted moult, S 6 remains unmoulted (Fig. 562) and in 20% S 5â&#x20AC;&#x201D;6 (see p, 15). The maximum was shown by a bird having S 3-6 and Al 1-2 unmoulted. Two birds interrupted P-moult: one bird had only P 9 unmoulted, another P 8-10, S 1-2 and Al 2-3. In NW Russia, one ad 9 was observed to retain P 10, two Al and some MaC (Rymkevich 1990). Prebreeding moult We have no indication of prebr moult. Senar (1988) reports moult of body-reathers in March from NE Spain and suggests that this may be a delayed moult of body-feathers which, similar to Loxia curvirostra^ could be related to the variable circannual cycle of the species. Comments on ageing Best criteria: Skull pneumatization until mid-September (p. 206). Most ly recognizable by moult limits within GC. Distinction between ly with all GC moulted and ad by moult limits within T, R, Al, S and P, but difficult when ly have all T and R moulted and skull'pneumatization completed. ly/2y: According to our data, 87% show an easily recognizable moult limit within GC. Juv GC and MeC have yellowish-white fringes and dark brown feather centres, postjuv. GC and MeC greenish-yellow fringes and black feather centres. The contrast between moulted and unmoulted MeC and GC is stronger in d than in ? (cf. Fig. 555 and 556). In spring, moult limits within GC are still recognizable despite
Fig. 551. ly in juv plumage, 5 August. Whole wing juv. Fringes of MeC, GC and T yellowish-white, fringes of MaC brownish.
Carduelis spinus
175
Fig. 552. ly & after partial postjuv moult, 28 October. MaC postjuv. MeC 4 postjuv, rest juv. GC and rest of wing juv. Rare case of ly with limited postjuv moult. Moult limits within MeC and between MeC and MaC distinct.
Fig. 555. ly $ after partial postjuv moult, 25 October. MaC and MeC postjuv. GC 1-2 juv, 3-10 postjuv. T 8 postjuv. Rest of wing juv. Distinct moult limits within GC and T. The renewed T 8 has a greenishyellow fringe and a darker feather centre than the juv T 7 and 9.
Fig. 553. 2y 6 after partial postjuv moult, at the beginning of its first postbr moult (Pi and P C I just shed), 5 August. MaC and MeC postjuv. GC 1-7+10 juv, 8-9 postjuv. Rest of wing juv. Moult limit within GC clearly visible even after about one year of wear. The renewed GC have a greenish-yellow fringe and dark feather centres, juv GC a yellowish-white fringe and slightly lighter feather centres.
Fig. 554. ly 9 after partial postjuv moult, 31 October. MaC postjuv. MeC 1 juv, 2—8 postjuv. GC 1—4 juv, 6-10 postjuv. Rest of wing juv. Easily recognizable moult limits within MeC and GC.
Fig. 556. ly 9 after partial postjuv moult, 13 September. MaC and MeC postjuv. GC 1—2 juv, 3—10 postjuv. T 7 juv, 8—9 postjuv. Rest of wing juv. In 9, the moult limits within GC and T are usually less conspicuous than in c5.
Fig. 557. ly 9 after partial postjuv moult, 11 October. MaC and MeC postjuv. GC postjuv. CC and Al juv. T postjuv. Rest of wing juv. Recognizable as ly by the slightly more pronounced difference in colour between the renewed T and S 6, as well as between GC and PC, than in ad (cf. Fig. 563).
176
Carduelis spin
Fig. 558. ly 6 after eccentric partial postjuv moult, 6 October, MaC, MeC and GC postjuv. CC postjuv. Al 1—2 postjuv, 3 juv. T postjuv. P 5—6 postjuv. Rest of wing juv. The eccentrically renewed P 5—6 are slightly darker and have a darker yellow spot on the outer web than the juv P 1-4.
Fig. 559. 1 y 9 after eccentric partial postjuv moult, 5 October. MaC, MeC and GC postjuv. CC and Al postjuv. T postjuv. P 5—7 postjuv. Rest juv. In 9 , the difference in colour of the yellow spot on the outer webs of juv and postjuv P is less pronounced than in 6 (cf. Fig. 558).
Fig. 560. ly £ after eccentric partial postjuv moult, 8 October. MaC, MeC and GC postjuv. CC and Al postjuv. T and S 5—6 postjuv, S 1-4 juv. P 1-2+5-" postjuv, 3-4+8-10 juv. PC juv. Rare case of a bird showing renewed P in two blocks. They are recognizable by their dark yellow outer web and slightly darker colour. The renewed S 5—6 contrast with the juv S in their darker feather centres.
Fig. 561. ly 6 after extensive partial postjuv P-moulr, 28 October. MaC, MeC and GC postjuv. CC and Al postjuv. T and S 1 +6 postjuv, 2-5 juv. P 1—8 postjuv, 9—10 juv. PC 1+5 postjuv, rest juv. Exceptional case of an almost complete postjuv moult.
Fig. 562. Ad cT after postbr moult interrupted at S 6, 26 October. S 6 remained unmoulted, rest of wing postbn Easily recognizable as ad by the retained S 6. No moult limits within MaC, MeC, GC, T and Al. All T and S similar in colour.
Fig. 563. Ad 9 after complete postbr moult, 19 October. Whole wing postbr. No moult limits within MaC, MeC, GC, T and Al. T and S, as well as GC and PC, more similar in colour than in those ly/2y having all GC and T renewed {cf. Fig. 557).
Carduelis cannabina
177
Carduelis cannabina Linnet Extent of postjuvenile moult MaC and MeC: all. GC: range 0-10, mean 7.2, mode 9, no GC 1.3%, all GC 13.5% (N= 630). CC: 8.0%. Al: none 94.4%, one 4.7%, two 0.9% (N=538). T: none 56.7%, one 10.2%, two 11.1%, three 22.0% (N=568) (see p. 33). R: none 50.4%, one 20.6%, two 12.5%, three 3.9%, four 3.5%, five 2.3%, six 6.7% (N=567) (see p. 34). P: Eccentric P-moult was recorded in 20 ly/2y (3.4%, N=586; see p. 36). Ten birds had P 6, five P 6—7 and three P 5—7 renewed, one bird P 6+9 and one P 1-2+5-7, respectively. Five of these had renewed P on one wing only. Most of them had all GC, CC, one or two Al, all T and all R moulted. PC were not moulted or not necessarily with the corresponding P.
The extent of postjuv moult is correlated among GC, CC, Al, T and R (Fig. 565). R may be moulted when at least five GC are renewed, T when at least six GC, and CC and Al when at least seven GC renewed. cT moult significantly more GC (mean 7.8, N=282), T (1.1) and R (1.4) than 9 (means GC 6.8, T 0.8, R0.9, N=345). Before autumn migration (during pre-migratory movements of local birds) and again during autumn migration, the extent of postjuv moult decreases with time (Fig. 566). In NW Russia, GC-moult is of similar extent (mean 7.4, range 6—8, N=47), but CC, Al and R are apparently not moulted (Rymkevich 1990). Among seven ly on the Balearic Islands, three were found with eccentric P-moult (Mester & Priinte 1982): two birds with P 6 and one with P 5—6 renewed. Svensson (1992) also mentions eccentric moult for Mediterranean populations. The rare cases of complete moult mentioned for England (Ginn & Melville 1983) are likely to be eccentrically moulting ly. Fig. 565. Relationships between the number of postjuv GC and the percentage of individuals with renewed CC, Al, T and R in ly/2y Carduelis cannabina which have completed their postjuv moult.
Fig. 566. Mean number of postjuv GC during autumn of ly Carduelis cannabina which have completed the postjuv moult (data grouped in five-day periods; the first value includes the period 19 August—7 September).
Fig. 564. Extent of postjuv moult on the wing and tail in ly/2y Carduelis cannabina.
Extent of postbreeding moult Whole plumage. Some birds migrate when still in the last stages of wing-moult (P 9 and/or S 5-6 growing), even as late as the end of October. Exceptionally, temporarily halted P-moult occurs (van Laeken & Caekebeke 1982). Comments on ageing Best criteria: Skull pneumatization until mid-October (p. 206). Most ly/2y recognizable by moult limit within GC, although moult limit within outer GC is not easy to detect. ly/2y with all GC moulted are distinct from ad in having moult limits within Al and R, between CC, Al and PC and between T and S. ly/2y: Birds which retain at least three juv GC (41%) are easily recognized (Fig. 568-571). Renewed GC are usually longer than juv GC and have only a narrow pale fringe. Juv GC are broadly tipped buffish and their outer web is lighter brown. Moult limits within GC 1—2 (46%) are more difficult to detect (Fig. 572 and 573) > mostly by slight differences in colour of the terminal fringe. Moult limits within GC can easily be recognized up to spring (Fig. 571) and often even during summer (Fig. 572). Birds with all GC moulted (13%) can be determined by moult limits within Al and R, between CC, Al and PC and between T 7 and S 6 (Fig. 574 and 575). Moult limits within T are often difficult to recognize. 65% of ly/2y with all GC moulted show a moult limit within R. Juv R are more pointed and more worn than postjuv R. A few birds can be recognized by eccentrically moulted P (Fig. 574 and 575). Ad: No moult limits within GC and in the area of CC, Al and PC. Outer fringes of T 7 and S 6 similarly worn and coloured. All R rounded.
1 8
Carduelis cannabina Fig. 571. 2y 9 after partial postjuv moult, 2 May. MaC and MeC postjuv. GC 1—3 juv, 4-10 postjuv. Rest of wing juv. Juv GC slightly shorter and looser, with paler terminal fringes and outer webs less brown than postjuv GC.
Fig. 567. ly in juv plumage, 4 August. Whole wingjuv. MeC and GC with huffish terminal fringes.
Fig. 568. ly 9 after partial postjuv moult, 18 October. MaC and MeC postjuv. GC 1-8+10 juv, 9 postjuv. Rest of wing juv. Renewed GC 9 without huffish terminal fringe and longer than juv GC.
Fig. 569. ly <5 after partial postjuv moult, 31 October. MaC and MeC postjuv. GC 1—7 juv, 8—10 postjuv. Rest of wingjuv. Renewed GC with only a narrow pale fringe, slightly longer and darker brown than juv GC.
Fig. 570. ly 6 after partial postjuv moult, 16 September. MaC and MeC postjuv. GC 1-4 juv, 5-10 postjuv. Rest of wing juv. Renewed GC darker brown and slightly longer than juv GC which show huffish tips.
Fig. 572. 2y 9 after partial postjuv moult, just before the first postbr moult, 10 August. MaC and MeC postjuv. GC 1—2 juv, 3—10 postjuv. Rest of wing juv. Plumage worn. Recognizable as 2y by the juv GC 1-2 which are more worn and looser than postjuv GC. This bird exceptionally has four T.
Fig. 573. ly <S after partial postjuv moult, 11 October. MaC and MeC postjuv. GC 1 juv, 2-10 postjuv. CC and Al 1 postjuv. Rest of wing juv. GC 1 identifiable as juv by its pale fringe. Moult limit within Al.
Carduelis cannabina
Fig. 574, ly 9 after eccentric partial postjuv moult, 12 October. MaC, MeC and GC posijuv. CC and Al 1 postjuv. T 7 postjuv, 8-9 probably also postjuv. P 6 postjuv. Rest of wing juv. Recognizable as ly by moult limits between the renewed CC and Al 1, and the juv Al 1-2 and PC. Moreover, the eccentrically moulted P 6 is darker, especially at the tip, than the adjacent P.
179
Fig. 576. Ad 9 after complete postbr moult, 19 October. Whole wing postbr. No moult limits in the area of GC, Al, CC and PC and between T 7 and S 6.
Fig. 577. Ad cT after complete postbr moult, 31 October. Whole wing postbr. No moult limits in the area of GC, Al, CC and PC and between T 7 andS6.
Fig, 575. ly d after eccentric partial postjuv moult, 14 October. MaC, MeC and GC postjuv. CC and Al 1 postjuv. T postjuv. P 6-7 postjuv. Rest of wing juv. Moult limits in the area of Al, CC and PC as well as between postjuv T and juv S are diagnostic of ly. The tips of the eccentrically moulted P 6-7 are darker than those of the adjacent P. P 7 has a pathologically luxuriated tip.
180
Carduelis flammea cabaret
Carduelis flammea cabaret Redpoll Extent of postjuvenile moult MaC and MeC: usually all. 17 with few or no GC moulted may retain one or a few juv MeC. GC: range 0-10, mean 2.8, mode 0, no GC 28.8%, all GC 0.7% (N=438). CC: 1.4% (N=358). Al: Al 1 is rarely renewed, but juv and postjuv Al are hardly distinguishable when full-grown. T: none 97.5%, one 1.4%, two 1.1%(N=363). T may be moulted when at least six GC, and CC when at least eight GC are renewed. The extent of postjuv moult decreases as the autumn migratory season proceeds (Fig. 579). In C. f. cabaret from Nottinghamshire, England, only a small proportion from early broods moulted some GC, while no renewal of T (contrary to Boddy 1981) and R was recorded (Boddy 1983). Similarly, Redpolls from Northumberland, England, only sometimes renew GC, never T and only one bird R (Evans 1966). In C.f flammea postjuv moult includes part or all MaC and MeC, usually four to five GC (range 0-10), sometimes the CC, rarely in early-hatched birds T and Al, but not R (Rymkevich 1990). According to Svensson (1992), one or two R may rarely be renewed. Extent of postbreeding moult Whole plumage. During the end of the breeding season (July, August), some birds may temporarily suspend P-moult, probably due to breeding (see p. 24). This seems to be a more frequent phenomenon than in other small passerines. Several birds were found to halt P-moult temporarily and show one or two almost full-grown P, but no other P in growth. Furthermore, two cT had P 1 renewed on both wings and one 2 with a brood patch P 1-2 on both wings, while the rest of the plumage consisted of old non-growing feathers. Similar observations are reported from Nottinghamshire, England (Boddy 1983). One bird from 2 November had retained Al 2 and S 6 (Fig. 587).
Fig. 578. Extent of postjuv moult on the wing and tail in ly/2y Carduelis flammea cabaret.
583), but this difference may be much less conspicuous, especially if the moult limit is among the outer GC (Fig. 584 and 585). Therefore, always check for differences in colour of the feather centres. Juv GC have paler, browner feather centres than postjuv GC. ly/2y with all (0.7%) or no GC moulted (29%) are difficult to distinguish from ad on plumage characters. The former may be recognized by moult limits within Tor between T and S, the latter by retained juv MeC (Fig. 581), if skull pneumatization cannot be used. Most ly can be recognized by having more pointed R than ad, and this is the main ageing criterion used by many ringers (Boddy 1981, Svensson 1992). Due to wear, ageing becomes progressively more difficult as spring approaches. Ad: No moult limit within GC and T. R more rounded than in ly/2y.
Comments on ageing Best criteria: Skull pneumatization until the end of October (p. 207). R of ly/2y usually more pointed than in ad. Moult limit within GC diagnostic of ly/2y. ly/2y with all GC juv or postjuv difficult to separate from ad. ly/2y: 70% show a moult limit within GC, recognizable by differences in colour of feather centres and tips between juv and postjuv GC. The colour of the tips of juv and postjuv GC varies between individuals. Generally, there is a tendency for tips of juv and exposed GC (GC 6â&#x20AC;&#x201D;9) to bleach more rapidly than postjuv and protected GC. In typical birds, juv GC have buffish tips, postjuv GC brownish-orange tips (Fig. 582,
Fig. 579. Mean number of postjuv GC during autumn of ly Carduelis flammea cabaret which have completed the postjuv moult (data grouped in five-day periods; the first value includes the period 30 Julyâ&#x20AC;&#x201D;2 September, the last 28 October-6 November).
Fig. 580. ly in juv plumage, 11 August. Whole wing juv. All GC uniformly brown with buffish tips. In this bird, the MeC show distinct fault bars.
Fig. 581, 1 y after partial postjuv moult, 31 August. MaC postjuv, MeC postjuv, except one juv. GC juv. Rest of wing juv. Recognizable as ly by the retained juv MeC. No moult limit within GC. The feather centres of all GC are similarly brown. The buffish tips of the inner, more exposed GC are worn and bleached.
Carduelis flammea cabaret
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Fig. 582. ly after partial postjuv moult, 23 October. MaC and MeC postjuv. GC 1-8+10 juv, 9 postjuv. Rest of wing juv. Recognizable as ly by the renewed GC 9 which is longer, has a darker feather centre and a more brownishorange tip than the adjacent juv GC with their slightly browner feather centres.
Fig. 583. 1 y after partial postjuv moult, 23 August. MaC and MeC postjuv. GC 1-6 juv, 7-10postjuv,GC10 growing. Rest of wing juv. Distinct moult limit within GC. Postjuv GC are slightly longer, have brownish-orange tips and darker feather centres than the juv GC.
Fig. 585. ly after partial postjuv moult, 9 September. MaC and MeC postjuv. GC 1-2 juv, 3-10 postjuv. T 7 juv, 8-9 postjuv. Rest of wing juv. Recognizable as ly by moult limits within GC and T. Juv GC 1-2 and juv T 7 have slightly browner and paler feather centres than postjuv. Tips of renewed T 8-9 brownish-orange, not buffish as in the juv T 7.
Fig. 586. Ad 6 after complete postbr moult, 19 October. Whole wing postbr. All GC have similarly coloured dark feather centres and brownishorange tips.
Fig. 584. ly after partial postjuv moult, 18 September. MaC and MeC postjuv. GC 1-4 juv, 5-10 postjuv. Rest of wing juv. Inconspicuous moult limit within GC. The GC 1-4 are recognizable as juv by their slightly paler, browner feather centres compared with the postjuv GC 5-10.
Fig. 587. Ad after complete postbr moult, 2 November. Whole wing postbr, except S 6 and Al 2. Exceptional case of an arrested moult.
182
Loxia curvirostra
Loxia curvirostra Crossbill Moult seasons and plumages Due to the variable breeding season, moult and plumages of the Crossbill exhibit a variability and complexity which is unusual for European passerines. The precise relationships between moult and other events of the life cycle have still to be discovered. The main moult season of ly and ad Crossbills is between late summer and late autumn (e.g. Weber 1953, 1972, Newton 1972, Rymkevich 1990, Fig. 590). During this period, part of the ad population perform a complete postbr moult and part of the ly a partial postjuv moult, as in other European Fringillidae. The remaining ad and ly, however, start moult earlier (probably in spring, cf. Berthold & Gwinner 1972 for ly, Rymkevich 1990 for ly and ad, but details unknown), then interrupt moult temporarily, before completing it during the main moult season. As regards P-moult of ad, about half of the individuals perform a complete postbr P-moult during the main moult season. The other half starts P-moult earlier (probably in spring; cf. Rymkevich 1990), suspends it and completes it during the main moult period. The reasons for an early first phase of P-moult are unknown, but might be related to the timing of breeding. According to Rymkevich (1990), Pmoult is supended due to breeding or in response to increasing daylength. Migration is probably another factor inducing suspension of P-moult, or at least a reduction of its speed (Williamson 1957a, Weber 1972). This is corroborated by our findings at Col de Bretolet where many birds were not moulting. Those which were moulting had only one or at most two P growing simultaneously and S-moult was rare (Fig. 590). Similarly, irruptive birds during summer in Mecklenburg (NE Germany) were not performing active moult (Weber 1972). As regards moult of ad in general (including body-feathers), it is still not clear whether or not all ad have two annual moult seasons, as suggested by the two circannual moult periods shown by caged birds held under constant conditions for up to four years (Berthold 1982) and whether or not one of these moult periods might represent a prebr moult, as described by Tordoff (1952, 1954) for L. c. benti (comprising part of the body-feathers). However, ad $ found in completely red and worn plumage before the main moult period in summer suggest that many ad perform only one moult annually. The reasons for an early onset of postjuv moult are more apparent, ly hatched during winter or early spring begin body moult earlier (probably in spring; cf. Berthold & Gwinner 1972, Rymkevich 1990) than ly hatched later (Weber 1972, Rymkevich 1990). However, as in ad, the reasons for interrupting an early started moult are still obscure. Another peculiarity of the Crossbill is the variable coloration of the 6 -plumage. Feathers replaced during summer and autumn (from June onwards according to Weber 1972; from the beginning of July according to Newton 1972) acquire a red colour and those growing outside this period, a yellow or yellowish-green colour. Thus, <3 moulting all feathers during the main moult season acquire a red plumage. Those moulting some of their feathers outside the main moulting season have a mixed yellow-red plumage by the end of this period. This variability in coloration is most conspicuous in bodyfeathers, but can also be traced in wing-coverts, T, P, S and R by the colour of the fringes. Thus, any yellow-green or red colour in 3 is no use as an ageing criterion. The change in <3 -colour occurs at the same time as the birds change from feeding on old to new cones (Newton 1972). Thus, dietary pigments may be responsible for the variability in c? -colour. However, observations on captive birds suggest that other factors may play a role as well (Weber 1953, Volker 1957).
The fact that the complex and variable moults of the Crossbill are not yet fully understood means that the correct naming of moults and plumages is difficult at present. We use the provisional terms 'first phase of postjuv/postbr moult' and 'main phase of postjuv/postbr moult', although the relationships to breeding are not known and the term 'postbr' may prove to be wrong for the first moult phase of some individuals. The two circannual moult periods of caged birds (Berthold 1982) would suggest the terms postbr and prebr moult. In ad suspending P-moult, it is not known whether the first phase of P-moult occurs before breeding (as stated by Rymkevich 1990; hence 'prebr moult', cf. Tordoff 1952, 1954) or after breeding but before migration (as suggested by birds caught on migration, Newton 1972; hence 'first phase of postbr moult'). The main moult period in autumn is likely to be a postbr moult (in those birds having one moult season annually) or a continuation of an interrupted postbr moult. The following account is based on 792 ad and 761 ly/2y caught between July and early November on Col de Bretolet. No year with a really large-scale irruption could be studied. Because we know of no published report on the extent of moult during winter and spring and because we cannot document this moult thoroughly either, the following account is provisional and may include inaccuracies. Moult during winter and spring and the relationship between moult and breeding are urgent priorities for further studies. Extent of postjuvenile moult Some birds start the postjuv moult before the main phase, interrupt it and continue during the main moult period (Weber 1972, Herremans 1988b, Rymkevich 1990). The facultative first phase of the postjuv moult is seasonally variable, depends on time of fledging (100â&#x20AC;&#x201D;110 days after fledging at the earliest, according to Rymkevich 1990) and may be of low intensity and extend over a long period (Weber 1972). Birds performing this first phase of postjuv moult have probably hatched during winter and early spring and may renew part of the body-feathers (exceptionally all) and sometimes a few MaC, MeC and one to three inner GC, but never CC, Al, T or R (Fig. 591). In cJ, feathers acquired during this first phase are yellow or yellowish-green. Birds in juv plumage with completely pneumatized skull and no growing feathers caught by us in July and August (12% of all caught in juv plumage, N=185) suggest that the first phase of postjuv moult may be completely suppressed in birds hatched during winter/spring or even earlier. Assuming a period of several months to complete skull pneumatization as in other Fringillidae (Winkler 1979), those birds would be about six months old. Two of these birds also showed a brood patch, suggesting breeding in juv plumage (see also Berthold & Gwinner 1972). During late summer and autumn, birds in juv plumage, with interrupted postjuv moult, in active postjuv moult or with completed postjuv moult were all found. Birds in complete juv plumage occurred from July until September (but not during October), 14% of them just starting postjuv moult (with only a few growing body-feathers). Birds in interrupted postjuv moult appeared from July until September in decreasing proportions. Birds in active postjuv moult appeared mainly during September and October (around 50% of all ly/2y caught during these months). Birds with their postjuv moult completed increased from August to the end of autumn. By October, almost all ly/2y had completed or almost finished their postjuv moult. The main phase of postjuv moult seems to be seasonally fixed, occurs at the same rime as in ad and progresses faster and with a higher intensity than the first phase of postjuv moult (see also Weber 1972). In cT, the feathers acquired during this phase are red. Thus, cT which do not perform the first phase of postjuv moult change from the juv plumage directly into a red plumage without acquiring yellowish feathers. During the main phase of postjuv moult, all body-feathers are renewed, but those replaced during the first phase are probably not replaced
Loxia curvirostra
183
again, because many $ with a mixed yellow-red plumage are seen in October. The extent of post] uv moult is probably related to hatching date. Birds hatched during winter (many probably performing a first phase of postjuv moult) have an extensive main postjuv moult sometimes including P, while birds hatched later renew only body-feathers and part of the wing-coverts (see also Rymkevich 1990). Birds which have completed the main phase of postjuv moult (ly birds in autumn and 2y birds before the first postbr moult) show the following extent of postjuv moult. MaC and MeC: frequently all. Individual juv MaC and MeC may be retained even in birds with most GC moulted. GC: range 0-10, mean 4.9, mode 6, no GC 10.6%, all GC 4.6% (N=197). CC: 4.7%. Al: none 94.7%, one 0.6%, two 0.6%, three (only in birds showing eccentric P-moult) 4.1% (N=171). T: none 66.9%, one 14.7%, two 9.2%, three 9.2% (N=184). R: none 88.2%, one 3.9% (always R 1), two to four 2.3%, six 5.6% (N=179). S: One bird with all P moulted had also renewed S 6. P: At least 8% renewed one to all P (N=197, see p. 36). This P-moult may be eccentric involving one to four central P (11 birds; Fig. 595), start at P 2, 3, 4 or 5 and proceed up to P 10 (five birds; Fig. 596) or may comprise all P (one bird; Fig. 597). Often, but less frequently than in other Fringillidae, birds with eccentric P-moult have renewed all GC,CC,A1,T,R. PC: In birds with renewed P, the corresponding PC are mostly not moulted or moulted irregularly. This is in contrast to ad performing partial P-moult, which generally renew the corresponding PC. The extent of postjuv moult is correlated among GC, T and R (Fig. 589). Herremans (1982, 1988b) found a similar extent of postjuv moult in Belgium. He found five ly/2y birds with a complete postjuv P-moult, one among them with all S renewed. Thus, a complete postjuv moult may occur. Usually, however, the first complete moult probably occurs only in the second summer/autumn, thus birds hatched in winter Fig. 589. Relationships between the number of postjuv GC and the percentage of individuals with renewed T and R in ly/2y Loxia curvirostra which have completed their main phase of postjuv moult.
Fig. 590. Monthly distributions of ad Loxia curvirostra on Col de Bretolet, Switzerland, according to the state of P-moult and percentage of ad in active S-moult (N=sample sizes).
Fig. 588, Extent of postjuv moult on the wing and tail in ly/2y Loxia curvirostra after the main phase of postjuv moult.
retain their juv wing-feathers for one and a half years and show very worn P in their second summer (Fig. 598). Extent of postb reeding moult P: In July (Fig. 590), only 15% were in active P-moult and only 2.3% had already renewed all P. The rest had either all P old (42.5%) or a suspended P-moult with outer P older than inner P (40.2%, Fig. 600). From this, we estimate that about half of the ad undergo a first phase of P-moult and then suspend P-moult before July. P-moult suspension is likely to occur in winter/spring since the difference in wear between inner and outer P is visible, but not striking, P are moulted predominantly between August and October (Fig. 590). It is likely that those which had interrupted P-moult after the first phase complete it in autumn, since by October, there are very few birds left with outer P older than inner P, while the proportion of birds with inner P older than outer P increases (Fig. 590 and 602), again showing only a slight difference in wear. Moreover, the proportion of birds with all P old in July is about the same as the proportion of birds having all P new in October. These represent the half of the ad which perform a complete P-moult in late summer/autumn without suspension, showing no trace of P-moult interruption (Fig. 603 and 604). A few birds have not started P-moult in October, but may still do so, since Pmoult is known to extend into early winter (Newton 1972). Of all birds with suspended P-moult (N=314), 72% renewed one to three P, 26% four to six P and 2% seven to nine P before suspension. PC: Generally, PC are renewed in the usual sequence together with the corresponding P. Thus, ad in P-moult suspension also show a suspension of a descendant PC-moult, in contrast to ly after partial P-moult. GC, CC, T, R: Birds performing a two-phase P-moult may, during the first phase, moult (often in irregular sequence) one to all GC, T, part of R, CC and part of the body-feathers together with the first few P before the main moulting period (Fig. 602). Moult of R during the main moult period is strongly correlated with P-renewal. R-moult starts with the shedding of P 2â&#x20AC;&#x201D;6 and is finished before all P are full-grown. S: The following evidence (see also Herremans 1982, 1988b) suggests that a remarkable percentage of ad moult S independently of the P and not necessarily at the same time (Fig. 601 and 603), as in some longdistance migrants. Furthermore, S-moult may be interrupted at any stage and often proceeds without a discernible sequence, resulting in two or three feather generations within S (Fig. 602). Since the S only wear a little, it is difficult to assign them to moult periods. As only a few ad were found with growing S (Fig. 590), even among those having
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Loxia curvirostra
outer P growing, it remains to be shown at which time of the year Smoult occurs, and when in relation to P-moult. Probably, S-moult is often protracted over two P-moult cycles. Birds with all P old (N=99) have all S old (80%), one to five S (17%) or rarely all S (2%, Fig. 601) renewed. Similarly, birds having up to four inner P renewed (in P-moult suspension) or growing (N=336) have all S old (88%), one to five S (12%) or rarely all S (1%) renewed. Of those ad having P 5-8 growing as the outermost P (N=56), only 11% were moulting S 1 or S 1-2, while 77% had all S old and 12% part of the S renewed (one additional bird had S 1 growing while in suspended P-moult with the inner six P renewed). Of those ad having P 9 growing as the outermost P (N=31) only 16% showed S 6 or S 5 growing together with a variable number of renewed S, while 61% showed old S and 23% part of the S renewed. Of birds with all P renewed (after a complete or a resumption of a suspended P-moult, N= 141), only 23% had allS renewed, 55% some (Fig. 602), 17% none (Fig. 603) and 5% had S 5 or 6 growing together with a variable number of renewed S.
Ad: No whitish fringes on MeC and GC, R rounded. Ad in P-moult suspension may show a moult limit within GC, but never show juv, whitish fringed GC. In ad cT, GC moulted during the first phase of postbr moult are fringed greenish, those renewed after July fringed red. Moreover, renewed S usually occur only in ad, and ad usually renew the PC corresponding to renewed P. PC of ad show no or only faint whitish fringes.
^Comments on ageing Best criteria: Whitish fringes on GC, CC and Al 1 diagnostic of ly/2y. ly/2y with all GC, CC and Al 1 renewed or after completion of an extensive or complete postjuv moult may be difficult to distinguish from ad (see below). Examination of skull pneumatization requires experience, because the scalp is relatively thick and the pattern of pneumatization often irregular. Birds with incompletely pneumatized skulls can be determined as being in their first year of life. ly/2y: Birds in juv plumage are easily recognized by their streaked blackish appearance. Birds hatched in winter after having undergone a first phase of the postjuv moult (probably in spring) often retain streaked juv bodyfeathers on the underparts and always at least some juv GC fringed whitish. After the main postjuv moult in autumn, those ly/2y which underwent a moderately extensive postjuv moult are easily recognized by retained juv GC, CC, Al and MeC, often presenting distinct moult limits. Juv GC and MeC have distinct whitish fringes (see also Phillips 1977, Herremans 1982, Herroelen 1983), which vary individually (Fig. 591-594). Birds with large, conspicuous white fringes on GC and MeC often have the T fringed whitish as well and resemble Loxia leucoptera (van den Berg & Blankert 1980, Berthold & Schlenker 1982, Olsen 1991). Whitish fringes on CC, Al and PC are also typical of ly/2y, but less distinct than on GC and can occur faintly in ad as well. Note that greenish fringes occur on feathers moulted before June/July in both ad and ly/2y cT and are not diagnostic of ly/2y. A supporting criterion is the shape of the R. Birds with distinctly pointed R are mostly ly/2y, those with more rounded R can be ad or ly/2y with moulted R. Birds with a few eccentrically renewed central P, retaining some juv outer P, are ly/2y (Fig. 595). ly/2y with all GC and all outer P renewed are often difficult to distinguish from ad which have completed a suspended P-moult and which also have inner P old and outer P new (cf. Fig. 596 and 602). In these ly/2y, fringes of juv PC are usually lighter than in ad and PC corresponding to the renewed P are usually not or irregularly moulted, while in ad PC are usually moulted together with the corresponding P. Even more difficult to separate from ad are ly/2y which renewed all P (Fig. 597). Some of them can be recognized by retained juv PC, CC and Al. Furthermore, ly/2y with renewed P only rarely have S moulted. Thus, birds with some new S are likely to be ad (Fig. 602). ly/2y which have performed a complete postjuv moult are inseparable from ad.
Fig, 591. ly S after partial postjuv moult, 8 August. MaC partly postjuv, undermost row juv. Rest of wing juv. GC and MeC show whitish terminal fringes, typical of juv plumage. This bird had renewed about half of the juv body-feathers with yellowish fringed ones, but showed no growing body-feathers. Thus, it had interrupted postjuv moult at an early stage before June/July and might have hatched in
Fig. 592. ly ÂŁ after partial postjuv moult, 25 October. MaC postjuv, except the two outermost juv. MeC 1-3 juv, 4-8 postjuv. GC 1-8+10 juv, 9 postjuv. Rest of wing juv. Juv MeC and GC with whitish terminal fringes. Postjuv MeC and GC 9 without white fringes and darker than juv GC and MeC. This S renewed all juv body-feathers with postjuv ones, most of them having yellowish-green, a few red, fringes.
Loxia curvirostra
Fig, 593. ly 6 after partial postjuv moult, 13 October. MaC and MeC postjuv. GC 1—4 juv, 5—10 postjuv, T 7 juv, 8—9 postjuv. Rest of wing juv. Distinct moult limit within GC and T. Postjuv GC without white fringes and darker than juv GC. This d renewed a large part of the wing-coverts and all juv body-feathers by red-fringed ones, thus probably after June/July,
Fig. 594. 2y d after partial postjuv moult. 11 August. MaC partly postjuv, undermost row juv. Rest of wing juv. Recognizable as 2y by having all MeC and GC fringed whitish, thus juv. Although heavily worn, MeC and inner GC show conspicuous white terminal fringes. This bird underwent a postjuv moult of limited extent, replacing body-feathers by red-fringed ones, thus probably in late summer or autumn last year. Since yellowish feathers are lacking, there was probably no moult in winter or spring.
185
Fig. 595. ly 9 after eccentric partial postjuv moult, 9 September. MaC postjuv, some juv in undermost row. MeC 1-2 juv, 3-8 postjuv. GC 1 juv, 2-10 postjuv. CC juv, Al 1-2 juv, 3 postjuv. T postjuv. P 1-2+7-10 juv, 3-6 postjuv. PC juv. S 1—6 juv. Recognizable as ly by the whitish fringed juv MeC 1—2, GC 1 and by the fact that the PC corresponding to the renewed P 3-6 have not been moulted. This bird, probably hatched in the preceding winter, is likely to have undergone the postjuv moult in two stages, because MeC 7—8, GC 3—9 and T 8-9 are slightly older than MeC 3-6, GC 2+10 and T 7. The first part of the postjuv moult might have occurred during late winter or spring. During the second part of postjuv moult in summer, also P 3—6 have been moulted eccentrically.
Fig. 596. ly 9 after eccentric partial postjuv moult, 18 September. MaC and MeC postjuv. GC postjuv. CC juv. Al and T postjuv. P 1—2 juv, 3—10 postjuv. PC 1—5+8 juv, 6—7 postjuv. S 1—6 juv. Similar case as in Fig. 595, but more extensive eccentric P-moult. Such birds, probably hatched during winter, which underwent an extensive eccentric moult up to P 10 are occasionally difficult to distinguish from ad which had continued a suspended P-moult (inner P older than outer P, cf. Fig. 602). This bird is recognizable as ly by the whitish fringed CC and the fact that only two of the PC corresponding to the renewed P 3—10 have been renewed.
186
Loxia curvirostra
Fig. 597. ly 9 after complete postjuv P-moult, 6 October. PC 1-3 and S 1-5 juv. Rest of wing postjuv. S 1-5 with growth bars situated at the same distance from the tip and PC 1-3 worn and not moulted with the corresponding P, indicating juv feathers. Because they are not heavily worn, this bird might have hatched during the preceding winter and undergone an almost complete moult during its first summer.
Fig. 598. 2y cT after partial postjuv moult and subsequent suspended postbr moult, 31 July. MaC and MeC postjuv. GC 1 juv, 5—6+8—10 postjuv, 2—4+7 postbr. CC and Al 1 unclear, Al 2-3 juv. T postbr. P 1-5 postbr, 6-10 juv. PC 1-4 postbr, 5-9 juv. S 1-6 juv. This bird is probably about a year older than those in Fig. 595 and 596 and lived through two winters (heavily worn P and S). MaC, MeC arid GC 5—6+8—10 are recognizable as postjuv by being more worn and fringed reddish. They have probably been renewed during summer/autum of the preceding year. During the postbr moult, probably during spring/summer of the current year, GC 2—4+7, T, fringed greenish, and P 1—5 have been renewed. Note that almost all PC corresponding to the renewed P have been renewed descendantly as well. Recognizable as 2y by the heavily worn outer P.
Fig. 599. 2y 9 after eccentric partial postjuv moult and subsequent suspended postbr moult, 31 July. MaC, MeC, GC 1-6+10, CC, Al, T 7+9 postjuv. GC 7—9 and T 8 are probably postbr, since they are slightly less worn. P 1—3 postbr, 4—5+7-10 juv, 6 postjuv. PC 1-3 postbr, 4-8 juv. S 1-6 juv, Similar case as in Fig. 598, but after a more extensive postjuv moult including P 6. Recognizable as 2y by the heavily worn juv P and S and the eccentrically renewed P 6.
Fig. 600. Ad cT in suspended postbr moult, 1 August. Moult suspended after renewal of P 1-4 and PC 1-4. Other feathers difficult to assign to distinct feather generations. PC 1-4 have been renewed together with the corresponding P, typical of postbr moult. GC 1-3+9 are older than the other GC and T 7 older than T 8-9. S 1 and 6 seem to be older than S 2-5.
Fig. 601. Ad 6 after separate moult of S 1-6, 31 July. S 1—6 are distinctly newer than the P and the wing-coverts, and thus have been renewed separately.
Loxia curvirostra
Fig. 602. Ad S after completion of a suspended postbr moult, 22 September. P 1-5 have been renewed before, P 6-10 after moult suspension. The degree of wear and the colour of the fringes indicate that the first part of moult occurred before June/July, was then suspended and completed during late summer. Thus, S 1, GC 1-9, CC and part of the MaC have probably been renewed together with P 1-5 (fringed greenish); S 2+5-6, T 7, Al, GC 10, MeC and part of the MaC together with P 6-10 (fringed red). S 3-4 originate from the postbr moult of the preceding year. T 8â&#x20AC;&#x201D;9 are difficult to assign.
Fig. 603. Ad 9 after postbr moult not including S 1â&#x20AC;&#x201D;6, 30 October. Except S 1-6, the whole wing is fresh and hardly worn, suggesting a complete moult during*this summer/autumn without including the S. This ad bird looks similar to the ly in Fig. 597, but shows no juv feathers: S 1-6 are broader and less bleached than in Fig. 597.
187
Fig. 604. Ad 6 after complete postbr moult, 19 September. Whole wing postbr. Since the whole wing is equally fresh, this bird underwent a complete moult without interruption.
188
Pyrrhula pyrrhula
Pyrrhula pyrrhula Bullfinch Extent of postjuvenile moult MaC and MeC: all. GC: range 4-10, mean 6.5, mode 7, all GC 1.6% (N=256). CC: one bird had renewed CC on one wing (N=229). T and R: In some birds, it is difficult to recognize whether T and R are juv or postjuv. In those birds for which this could be distinguished and in birds with growing T, we found that less than 10% renewed T 7, about 50% T 8 and over 90% T 9. Only three birds renewed one to four R which might be due to accidental loss (N=133).
$ moult slightly more GC (mean 6.6, N=123) than ? (mean 6.3, N=133), but the difference is not significant. The extent of postjuv moult decreases as the autumn migratory season proceeds and remains at a moderate level during winter, spring and the breeding season (Fig. 606). In NW Russia, the postjuv moult may include GC, T, Al and CC, but not R (Rymkevich 1990). In England, five to ten GC are moulted and more than 50% of ly moult all GC according to Newton (1966, see also Svensson 1992), but Spencer & Mead (1978b) report that juv GC are present in almost all ly, more like our observations. In England, the CC is renewed only exceptionally (Newton 1966); three out of several hundred ly were found with a renewed CC, one with all GC renewed, the other two with some juv GC left (Flegg & Matthews 1980). T 8-9 are reported not to be moulted by Newton (1966). The extent of postjuv moult depends on hatching date (Newton 1966, Rymkevich 1990): ly starting postjuv moult in July and August moult more GC than birds starting later. A difference in the extent of GCmoult between the sexes was also found by Newton (1966).
Fig. 605. Extent of postjuv moult on the wing and tail in ly/2y Pyrrhula, pyrrhula.
610). Birds with a moult limit among outer GC and those with all GC moulted can be recognized by observing Al 1, which is always juv, and CC, which is juv in almost all birds. Juv CC and Al 1 show ill-defined, mostly brownish fringes fading into the feather centre. There are, however, birds having juv CC and Al 1 fringed greyish, but still illdefined. Wear and bleaching is very slight, so that 2y can be aged until the first complete postbr moult. Juv T 9 have a brownish or greyish outer web, postjuv and postbr T 9 usually a red or reddish, sometimes greyish, outer web in both sexes and age groups. Ad: All GC tipped greyish-white. CC with a distinct white or light grey fringe (Fig. 611). Al 1 usually with a distinct greyish-white fringe.
Extent of postbreeding moult Whole plumage. Ad with growing remiges occur regularly up to November, occasionally until December (Newton 1966). Comments on ageing Best criteria: Skull pneumatization until the end of October (p. 207). Moult limit within GC and ill-defined, often brownish fringe on CC andAl 1 diagnostic of ly. ly/2y: According to our data, 98% show a moult limit within GC. Although the colour of the tips of GC varies between individuals (cf. Fig. 607 and 608), moult limits are easily recognized. Juv GC have duller feather centres and usually slightly brownish tips (Fig. 609 and
Fig. 607. ly in juv plumage, 5 August. Whole wing juv. All GC, CC and Al 1 tipped brown. The juv T 9 has a greyish base and a brownish outer fringe.
Fig. 606. Mean number of postjuv GC in the course of the year of ly/2y Pyrrhula pyrrhula which have completed the postjuv moult (the two values for October refer to the first and second half of the month).
Pyrrhula pyrrhula
189
Fig. 608. ly in juv plumage, 2 August. Whole wing juv. Outer GC tipped whitish with only a slight brownish tinge. CC and Al 1 tipped brownish, typical of juv feathers. Juv T 9 with greyish base on outer web.
Fig. 610. 2y $ after partial postjuv moult, 3 May. MaC and MeC postjuv. GC 1—4 juv, 5-10 postjuv, T 9 postjuv. Rest of wing juv. Juv GC with duller feather centres than postjuv GC. CC and Al 1 fringed brownish. The postjuv T 9 has a red base on outer web. In spring, feathers are generally hardly worn.
Fig. 609. ly 9 after partial postjuv moult, 2 November. MaC and MeC postjuv. GC 1-5 juv, 6-10 postjuv. T 9 postjuv. Rest of wing juv. Distinct moult limit within GC. Juv GC 1-5 contrast with postjuv GC in their duller feather centres and smaller, slightly buffish tips. Al 1 and CC fringed brownish. The postjuv T 9 has a red base on outer web.
Fig. 611. Ad <5 after complete postbr moult, 31 July. Whole wing postbr. The feathers are only slightly worn even after the breeding season, just before the next complete postbr moult. All GC tipped greyishwhite. CC with welldefined whitish fringe. Al 1 fringed greyish not brownish.
Coccothraustes coccothraustes Hawfinch Extent of postjuvenile moult
MaC and MeC: all. GC: range 7-10, mean 9.9, mode 10, all GC 91.9% (N=62). CC: 85.0%. Al: none.59.3%, one 35.6%, two 5.1% (N=60). T: none 3.4%, one 8.6%, two 15.5%, three 72.4% (N=58). R: none 25.0%, one 41.1%, two 21.4%, four 1.8%, five 1.8%, six 8.9% (N=56). Extent of postbreeding moult
Whole plumage. Ad with S 6 still growing can occur until the end of October. One ad 2 with a brood patch still visible on 7 September had interrupted moult after renewing P 1—6, PC 1—5, S 1, T 8—9 and Rl-3. Comments on ageing
Best criteria: No easily applied single criterion. The combined checking of the points mentioned below should, however, enable determination of the age of most birds. Skull pneumatization not observable in live birds because the jaw muscles cover much of the skull.
Fig. 612. Extent of postjuv moult on the wing and tail in ly/2y Coccothraustes coccothraustes.
ly/2y: Only about 8% are recognizable by moult limits within GC (Fig. 614), the others renew all GC. Moult limits within other feather tracts are most easily seen among Al (Fig. 616) and R. Over 80% have a moult limit within R, which is recognizable by differences in feather wear and shape, Juv R are more pointed and narrower than postjuv, Moult limits within T are difficult to see. The criteria used up to now (Drost 1940, Mayaud 1941, Herremans 1990a) may help as well and are based on differences in shape and gloss of P 2-9. In ly/2y, the
190
Coccothraustes coccothraustes
metallic black gloss on P-tips is usually conspicuous on P 2-6, faint on P 7, and absent on P 8—9. The tips of P 3—5 are less curved in ly/2y and their inner webs less deeply indented than in ad (cf. Fig. 616 and
617). Ad: Al jet black without brownish hue. Gloss on P-tips always conspicuous up to P 7, in most ad up to P 8, sometimes up to P 9. P 3-5 strongly curved and tip of inner web deeply indented (Fig. 617 and 618). In autumn, also check for the last signs of P- and S-moult, especially growing S 6.
Fig. 616. ly 9 after partial postjuv moult, 30 September. MaC, MeC and GC postjuv. CC postjuv, Al 1 postjuv, 2-3 juv. T postjuv. Rest of wing juv. Moult limit within Al. Tips of P 3—5 only slightly curved, and inner webs only slightly indented. Gloss on tips of P 6 only faint, absent on P 7.
Fig. 613. ly in juv plumage, 29 July. Whole wing juv. Juv MeC and GC differ in colour from postjuv MeC and GC.
Fig. 614. 2y 6 after partial postjuv moult, 9 February. MaC and MeC postjuv. GC 1—2 juv, 3—10 postjuv. Rest of wing juv. One of the rare ly/2y with a moult limit within GC.
Fig. 617. Ad 9 after complete postbr moult, 22 October. Whole wing postbr. Al darker than in ly, tips of P 2—5 strongly curved and their inner webs deeply indented. Gloss on tips of P 6 and 7 conspicuous.
Fig. 615. ly 9 after partial postjuv moult, 6 October. MaC, MeC and GC postjuv. CC postjuv. Al juv. T 7 juv, 8-9 postjuv. Recognizable as ly because of the brown hue on Al.
Fig.6l8.Ad<3 after complete postbr moult, 21 October. Whole wing postbr. Al jet black, tips of P 2-5 strongly curved and inner webs deeply indented Gloss on tips of P 6 and 7 conspicuous.
Emberiza citrinella
191
Emberiza citrinella Yellowhammer Extent of postjuvenile moult MaC and MeC: all. GC:aIl(N=56). CC: 48.8%. Al: none 30.2%, one 62.8%, two 4.7%, three 2.3% (N=43). T: none 32.4%, one 24.3%, two 29.7%, three 13.5% (N=37). R: none 84.0%, one 14.0%, three 2.0% (N=50).
Rymkevich (1990) observed moult of all MaC, MeC, GC and CC and in four out of 140 ly of Al 2 or Al 2-3 in NW Russia. British birds are also reported to moult all GC (Snow 1967), although Ginn & Melville (1983) mention that probably not all GC are moulted. According to Svensson (1992), all R may rarely be moulted. The statement by Drost (1969) that Yellowhammers perform a complete postjuv moult is due to a misinterpretation of the unusual skull pneumatization in this species (Winkler 1976). Extent of postbreeding moult Whole plumage. One cT from 7 August suspended P-moult after renewal of P 1-4 (Herroelen 1980). Extent of prebreeding moult
Fig. 619. Extent of postjuv moult on the wing and tail in ly/2y Emberiza citrinella.
Fig. 620. ly in juv
plumage, 28 July. Whole wing j uv, remiges not yet Rillgrown.
The juv MeC and GC
have a whitish terminal fringe.
We have indications that during spring some birds renew some feathers of the head and upperparts, but not of the wing (five out of 44 birds). Similarly, Kasparek (1981) mentions that some birds renew part of the body-feathers (see also Svensson 1992 and Busse 1984), but this was not found by Rymkevich (1983). Comments on ageing Best criteria: Skull pneumatization until the end of November. Because about half of the ad never complete skull pneumatization, but remain at score 5 or 6, only scores 1â&#x20AC;&#x201D;4 are diagnostic of ly/2y (Winkler 1976, 1979, p. 207). Plumage characters difficult to apply. ly/2y: According to our data, ly moult all GC, thus moult limits within GC are likely to be rare. The innermost GC are usually fringed darker in both ly/2y and ad and may simulate a moult limit. Moult limits occur within Al and T as well as between CC and PC and between T and S, but are rather difficult to detect. If Al 1 has been renewed, its fringe is tinged greenish like the adjacent MaC and contrasts slightly with the buffish fringe of the juv Al 2 (cf. Fig. 621 and 622). However, ly/2y with Al 1â&#x20AC;&#x201D;2orAl 1-3 renewed occur as well. Juv and postjuv T are very similar in colour, thus moult limits within T can only be recognized by differences in wear (cf. Fig. 622 and 623). As an additional ageing criterion, the shape of the R is often helpful. Usually, the R of ly/2y are pointed, those of ad more rounded. There are, however, ly/2y with slightly rounded R which cannot be distinguished from those R of ad which are less rounded than usual. Moult limits within R are easily recognized by differences in wear, but occur only in a few ly/2y. The extent of white as well as the pattern of brown on R 5 and R 6 are highly variable between individuals and we were unable to detect consistent differences between ly/2y and ad as suggested by Norman (1992). Ad: No moult limits within Al, T, R and between T and S. Fringes of Al 1 and 2 of similar colour (Fig. 624). R usually rounded (but see above) and P in autumn usually less worn than in ly.
Fig. 621. ly 9 after partial postjuv moult, 1 November. MaC and MeC postjuv. GC postjuv. Rest of wing juv.
Al 1 has not been renewed and is fringed buffish as Al 2. The innermost three GC are slightly longer and fringed darker than GC 1-7, thus might simulate a moult limit. Since there are no differences in wear, all GC axe of the same generation.
192
Emberiza citrinella
Fig. 622. ly cT after partial postjuv moult, 20 October. MaC and MeC postjuv. GC and CC postjuv. Al 1 postjuv, 2â&#x20AC;&#x201D;3 juv. T and rest of wing juv. The renewed Al 1 is fringed greenish, like the adjacent MaC, and contrasts with the juv Al 2 fringed huffish. The juv T are worn and slightly pointed.
Fig. 623. ly 6 after partial postjuv moult, 20 October. MaC and MeC postjuv. GC and CC postjuv. AJ 1 probably postjuv, 2-3 juv. T postjuv. Rest of wing juv. Renewed T rounded and not worn.
Fig. 624. Ad 9 after complete postbr moult, 1 November. Whole wing postbr. P fresh and less worn than in ly/2y. No moult limit within Al and T. Note that GC 8-10 are slightly darker fringed than GC 1-7 and may simulate a moult limit as in ly/2y (cf. Fig. 621).
Emberiza cia
193
Emberiza cia Rock Bunting Extent of postjuvenile moult MaC and MeC: all. GC: range 6-10, mean 9.8, mode 10, all GC 93.3% (N=45). CC: 70.5%. Al: none 29.5%, one 65.9%, two 4.5% (N=44). T: none 44.4%, one 15.6%, two 31.1%, three 8,9% (N=45) (see p.
33). R: none 93.0%, one 4.7%, two 2.3% (N=43). Extent of postbreeding moult Whole plumage.
Fig. 625. Extent of postjuv moult on the wing and tail in ly/2y Emberiza cia.
Comments on ageing Best criteria: Skull pneumatization until winter (p. 207). Moult limits within T, between T and S as well as between CC, Al and PC diagnostic of ly/2y. ly/2y: A few ly/2y show a moult limit within GC, which is easily recognized (Fig. 627): juv GC have lighter and greyer feather centres than postjuv GC. The majority of ly/2y moults all GC and is recognized by moult limits within T and Al (Fig. 629 and 630) or between T and S as well as by moult limits between GC, CC, Al and PC (Fig. 628). Postjuv T have broader and, in autumn, more rusty fringes than juv T (Fig. 629 and 630). Juv Al 1-2 and PC are tinged brownish and contrast with renewed GC, CC and Al 1 which have more blackish feather centres (Fig. 628). In particular, the central R are generally more pointed than in ad and R 4 shows no white tip (Schuphan & Heseler 1965). However, these criteria are no longer useful in spring due to wear. Ad: No moult limits within GC, T, Al and between GC, CC and PC. Difference in colour of feather centres of GC, CC, Al and PC only slight (Fig. 632). R 4 tipped white. At least in autumn, S fringed rusty, not buffish as in ly (cf. Fig. 631 and 629, but see Fig. 626). According to Schuphan & Heseler (1965), ad have a reddish, ly an olive-brown iris.
Fig. 626. ly at the beginning of partial postjuv moult, 24 August. MaC postjuv, undermost row juv. MeC, GC and rest of wing juv. Note the rusty fringes of fresh juv T and S which bleach to huffish in autumn (cf. Fig. 629).
Fig. 627. ly 9 after partial postjuv moult, 2 November. MaC and MeC postjuv. GC 1â&#x20AC;&#x201D;4 juv, 5-10 postjuv. Rest of wing juv. Rare case of a ly with a moult limit within GC. The juv GC have lighter feather centres and are shorter than the postjuv GC.
Fig. 628. ly after partial postjuv moult, 5 October. MaC and MeC postjuv. GC postjuv. CC postjuv. Al 1 postjuv, 2-3 juv. T 7 juv, 8â&#x20AC;&#x201D;9 postjuv. Rest of wing juv. The postjuv CC and Al 1 have distinctly darker feather centres than the juv PC and Al 2-3. Postjuv T 8-9 have broader and more rusty fringes and darker feather centres than the juv T 7.
194
Emberiza cia
Fig. 629. ly 9 after partial postjuv moult, 27 October. MaC and MeC postjuv. GC postjuv. CC postjuv. Al 1 postjuv, 2-3 juv. T 7-8 juv, 9 postjuv. Rest of wing juv. Distinct moult limit within T. Postjuv T 9 fresh with broad rusty fringe, juv T 7-8 worn and fringed huffish. The renewed CC and Al 1 are darker than the juv Al 2-3 and the PC.
Fig. 631. Ad cJ after complete postbr moult, 2 November. Whole wing postbr. No moult limits within GC and T, nor between T and S. More similar colour of feather centres among CC, Al and PC. Fringes of S 1-6 rusty, not huffish as in ly autumn birds.
Fig. 632. A d d after complete postbr moult, 5 April. Whole wing postbr. Recognizable as ad by the absence of moult limits and the more homogeneous colour of CC, Aland PC compared to 2y.
Fig. 630. 2y S after partial postjuv moult, 28 April. MaC and MeC postjuv. GC postjuv. CC postjuv. Al 1 postjuv, 2â&#x20AC;&#x201D;3 juv. T 7 juv, 8â&#x20AC;&#x201D;9 postjuv. Rest of wing juv. Recognizable as 2y by the moult limit within T and the more pronounced difference in colour of the feather centres between the postjuv CC and Al 1 and the juv PC and Al 2. Postjuv T and GC less worn than juv T 7.
Emberiza hortulana
195
Emberiza hortulana Ortolan Bunting Extent of postjuvenile moult Body-feathers: about 10% retain some juv body-feathers, at least on upperparts. MaC: all. MeC: usually all. ly with no GC moulted may retain single juv MeC. GC: range 0-10, mean 2.4, mode 0, no GC 38.0%, all GC 8.9%. GC are often moulted in irregular sequence (N=79). CC: 6.3%. Al: none 93.7%, one 6.3% (N=48). T: none 92.6%, one 5.6%, two 1.9% (N=54). R: one bird renewed R 1 (N=54). The extent of postjuv moult decreases as the autumn migratory season proceeds (Fig. 634). A similar extent of postjuv moult was found by Rymkevich (1990) in NW Russia. Extent of postbreeding moult The postbr moult is usually interrupted before autumn migration and part or all S remain unmoulted. All birds examined in Switzerland had interrupted the postbr moult by renewing all P, R and usually T, but retaining two to six S (mean 4.3 unmoulted S, N=30; see p. 15): 13 birds retained S 2—6, six birds S 3—6, five birds S 3—5, one bird S 4—6, two birds S 4—5 and three birds S 1—6. In one bird (S 1—6 unmoulted), T 9, GC 8, some MaC and MeC were also retained, in another (S 1—6 unmoulted) GC 1 and the undermost row of MaC, and in two other birds (S 2—6 unmoulted) individual MeC. Two migrants had P 9 and S 6, respectively, still growing. Likewise, all ad showed moult interruption within S in Silesia (Natorp 1925), and among 101 autumn migrants from Sudan all had three to five unmoulted S (Nikolaus & Pearson 1991). A minority perform a complete postbr moult before autumn migration (Svensson 1992). According to Rymkevich (1990), ad moulting in June perform a complete postbr moult or may retain some S and GC, while ad moulting in July do not moult S and may retain GC, Al and MaC. Comments on ageing after postjuvenile and postbreeding moult Best criteria: Skull pneumatization at least during the whole autumn migration period in Europe (p. 207). Since three ad were found with incomplete skull pneumatization (score 5), only birds with scores 1^4 should be determined as ly. Juv GC usually diagnostic of ly, moult interruption within S usually diagnostic of ad. ly: 91% retain one to ten juv GC, which can be recognized by their whitish outer fringes (Fig. 635-637). Moult limits within GC are easily recognized by differences in wear, colour of the fringes and feather centres (Fig. 636 and 637). ly with all GC renewed (9%) are difficult to separate from ad which have performed a complete moult, except by
Fig. 633. Extent of postjuv moult on the wing and tail in ly Emberiza hortulana.
skull pneumatization. ly never show a strong contrast in wear within S or between S and P. Ad: According to our data, all ad retain unmoulted S which are conspicuously worn and bleached (Fig. 638 and 639). Ad having performed a complete postbr moult are best recognized by skull pneumatization. Extent of prebreeding moult: 2y and ad The following account is based on ten ad and five 2y only, thus is provisional. MaC: none or part. MeC: none, part or all. GC: range 2—10. It seems that 2y moult on average more GC (three birds all) than ad (only one bird all). CC: renewed by one ad only. Al: Al 1 was renewed by one 2y (Fig. 640). T: all. R: 0—6: none seven birds, R 1 four birds, R 1—2+5—6 one bird, all one bird. S: In birds in which the age was ascertained by ringing, all ad renewed 3-6 S, all 2y no S. Stresemann & Stresemann (1969b) mention moult of body-feathers and indicate that ad may perhaps moult retained S during winter. According to Rymkevich (1983, 1990), 2y moult body-feathers, GC, MeC, T, some R and other wing-coverts, ad the body-feathers, part of the wing-coverts, some R and those S not moulted during the postbr moult. This agrees well with our findings. Thus, ad Ortolan Buntings possibly resume moult of the secondaries at the point of interruption and perform a partial prebr moult in the winter quarters (cf p. 21). Comments on ageing after prebreeding moult
Fig. 634. Mean number of postjuv GC during autumn of ly Emberiza hortulana which have completed the postjuv moult (data grouped in five-day periods; the first value includes the period 9-28 August, the last 18-27 September).
Ageing spring birds is very difficult, since differences in wear and bleaching between feather generations are only slight. 2y which show very worn juv GC are most easily recognized, but probably rare. The difference in wear of P and S between ad and 2y are very inconspicuous. Since we recorded prebr S only in ad, we presume that this is diagnostic of ad. However, this remains to be checked on a larger sample of birds. Moreover, prebr S are difficult to detect: best features are slightly browner colour and slightly less wear. Ad which underwent a complete postbr moult are likely to be almost inseparable from 2y.
196
Emberiza hortulana Fig. 635. ly after partial postjuv moult, 7 September. MaC and MeC postjuv. Rest of wing juv. No moult limit within GC. Recognizable as ly by the whitish fringes on the juv GC which contrast with the huffish fringes of the postjuv MeC.
Fig. 636. ly after partial postjuv moult, 7 September. MaC and MeC postjuv. GC 9 postjuv, 1-8+10 juv. Rest of wing juv. Distinct moult limit within GC. The renewed GC 9 is fringed huffish to chestnut-brown and contrasts with the whitish fringed juv GC.
Fig. 638. Ad 9 after postbr moult interrupted within S, 14 September. Whole wing postbr, except S 2-6 and MeC 2. The retained S 2â&#x20AC;&#x201D;6 are conspicuously worn and bleached and diagnostic of ad.
Fig. 639. Ad after postbr moult interrupted within S, 7 September. Whole wing postbr, except S 3-5. Recognizable as ad by the interrupted S-moult. This bird renewed part of the S convergently.
Fig. 637. ly after partial postjuv moult, 18 September. MaC and MeC postjuv. GC 2-3+7-10 postjuv, 1+4-6 juv. Rest of wing juv. Recognizable as ly by the distinct moult limit within GC and the whitish fringes on juv GC. GC are often moulted in irregular sequence.
Fig. 640. 2y 9 after partial prebr moult, 9 May. MaC mostly prebr, rest postjuv. MeC and GC prebr. CC juv, T prebr. Al 1 prebr, 2-3 juv. Rest of wing juv. Recognizable as 2y by the worn and bleached A12-3.
Emberiza hortuiana
Fig. 641. 2y $ after partial prebr moult, 22 May. MaC and MeC postjuv. GC prebr. CC and Al juv. T prebr. Rest of wing juv. S and P more worn and bleached than in ad. Note that S 6 is slightly more abraded than S 2—5 which is probably due to its exposure during the renewal oftheT(cf.Fig.4l4).
Fig. 642. Ad S after partial prebr moult, 22 May. MaC and MeC postbr. GC 1-6 postbr, 7-10 prebr. CC and Al postbr. T prebr. S 1 postbr, 2-6 prebr. P and PC postbr. The prebr S 2—6 are slightly less worn and darker than the postbr S 1. Within S 2-6, wear gradually increases towards S 6 which is probably due to differences in exposure, especially during the renewal of the T.
197
Fig. 643. Ad 6 after partial prebr moult, 22 May. MaC postbr. McC prebr. GC 1-5+9-10 postbr, 6-8 prebr. CC and Al postbr. T prebr. S 1—4 prebr, 5-6 postbr. P and PC postbr. The prebr S 1—4 are less worn and slightly darker than the postbr S 5-6.
198
Emberiza schoeniclus
Emberiza schoeniclus Reed Bunting Extent of postjuvenile moult MaC and MeC: all. GC:all(N=316). CC: 96,0%. Al: none 41.4%, one 50.7%, two 5.0%, three 2,9% (N=278). T: none 15.4%, one 12.9%, two 42.1%, three 29.6% (N=311) (see p.
33). R: none 52.1%, one 11.9%, two 7.0%, three 4.2%, four 2.4%, five 2.8%, six 19.6% (N=286) (see p. 34). S and P: five ly/2y renewed S 6 (2.1%, N=240) together with all T, one of these also P 7 on one wing (eccentric P-moult). The extent of postjuv moult is correlated among T, Al, CC and R. In c? postjuv moult is slightly more extensive than in $, but significant differences between the sexes were only found in Al: 66.7% of the <J renewed at least one Al, but only 48.4% of the 9 (N=105 and 126, respectively). The extent of postjuv moult decreases as the autumn migratory season proceeds (Fig. 645). In NW Russia, only two out of 435 ly renewed R 1 (Rymkevich 1990). In Sweden, usually all GC are moulted, but only 17% (compared with 30% in Switzerland) renewed all T and only 7.6% (19.6% in Switzerland) all R; c? renewed all R more often (13%, N=96) than $ (6%, N=245; Karlsson et al 1985). Indications from Great Britain suggest that not all British birds renew all GC (Bell 1970, Ginn & Melville 1983). Whether or not occasional complete postjuv moult (Ginn & Melville 1983) really occurs remains to be confirmed. Extent of postbreeding moult Whole plumage Comments on ageing Best criteria: Skull pneumatization until mid-October (p. 207). Moult limits within T, R and Al and between T and S diagnostic of ly/2y, but often difficult to recognize. ly/2y: Ageing according to plumage characters is often difficult and requires experience. Thus, in autumn rely on skull pneumatization. Since ly/2y renew all GC (but possibly not always all in Sweden and Great Britain), ageing on plumage characters must rely on moult limits within T, R, Al and between T and S. 55% of ly/2y show a moult limit within T, 30% between T and S. Postjuv T have jet black feather centres, broader, more squared ends and are less worn than juv T (Fig. 648). Juv T are narrower and have slightly less deep black feather centres (Fig. 647). Note, however, that T 7 sometimes appears to have a slightly less dark feather centre than the other T of the same feather generation (Fig. 647). The light yellowish outer fringes of very fresh juv T 8-9 bleach to white during summer; thus a small white outer fringe Fig. 645. Mean number of postjuv T- plus R (of one side) during autumn of ly Emberiza schoeniclus which have completed the postjuv moult (data grouped in five-day periods; the first value includes the period 14 August-22 September).
Fig. 644. Extent of postjuv moult on the wing and tail in ly/2y Emberiza schoeniclus.
in autumn is often diagnostic of juv T (Fig. 647). During winter, however, the fringes of postjuv T and of ad T also bleach and this criterion is no longer valid. Other ageing criteria are moult limits within Al, which are difficult to recognize, and moult limits within R (28% of ly/2y), Juv R are pointed, renewed R more rounded. However, about 20% of ly/2y moult all R and cannot be separated from ad by this criterion. The PC of ly/2y are on average more loosely textured and slightly more worn than in ad (Karlsson et al. 1985), but due to considerable overlap between the age classes this is, according to our experience, only a supporting criterion. According to Karlsson et al. (1985), the iris in ly is dark grey, in ad tinged brown. During spring the iris in 2y is dark grey or tinged brownish, but darker and less brownish than in ad. In spring, ageing becomes even more difficult due to progressive wear and the characteristics of the R are unreliable. Only differences in colour of the feather centres between juv and postjuv T and between postjuv T and S are usually still easily recognized in spring (Fig. 649). Ad: No moult limits within T, Al and R and between T and S. P and S bleach and wear less quickly than in ly/2y and show the same feather centre colour as the T. Al 3 is usually darker than in ly. Iris colour and PC see above. Extent of prebreeding moult The prebr moult is of very limited extent and seems to include mainly all or part of the head-feathers (Poulsen 1950, Rymkevich 1983). Rare cases of birds renewing individual or even all R (Bell 1970) may be due to accidental loss.
Fig. 646. ly during partial postjuv moult, 25 August. MaC mostly postjuv. MeC, GC and rest of wing juv. Juv MaC, MeC and inner GC show yellowish, not chestnut-brown fringes.
Emberiza schoenidus
199
Fig. 647, ly 9 after partial postjuv moult, 28 October. MaC and MeC postjuv. GC and CC postjuv. Al juv. T and rest of wing juv. Juv T worn (more than GC) and slighdy pointed. T 9 shows a white outer fringe. Almost no difference in colour of the feather centres between T 7 and S. Note that T 8—9 often appear slightly darker than T 7 although they are of the same feather generation.
Fig. 649. 2y 9 after partial postjuv moult, 23 April. MaC and MeC postjuv. GC and CC postjuv. Aljuv. T 7 juv, 8-9 postjuv. Rest of wing juv. Recognizable as 2y by the moult limit within T. Postjuv T 8—9 have darker feather centres than juv T 7.
Fig. 648. ly 9 after partial postjuv moult, 13 October. MaC and MeC postjuv. GC and CC postjuv. Al 1—2 postjuv, 3 juv. T postjuv. Rest of wing juv. Recognizable as ly by the difference in colour of the feather centres between the postjuv T and the juv S. Postjuv T broad, almost squared and not worn.
Fig. 650. Ad <S after complete postbr moult, 22 October. Whole wing postbr. No difference in colour between the broad T and the S. P almost unworn, Al 3 darker than in ly.
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Appendix The use of skull pneumatization for ageing The process of skull pneumatization Passerines are characterized by a highly pneumatized skull, which develops during the first months of life. After fledging, the skull roof consists of a single layer of bone. A second bone layer is formed under the original skull roof, generally starting in the occipital region and ending at the forehead. The two layers are kept apart by tiny bony struts. The air circulating between the two layers is supplied via the airsacs of the nasal and tympanic cavities. For our purpose, the term pneumatization denotes the air-holding, double-layered state of the skull roof as well as the process leading from the unpneumatized to the pneumatized skull roof. The best term to describe the changes taking place within the skull roof of juvenile passerines is pneumatization, rather than the widely used term ossification, especially since the skull roof is already bony (i.e. ossified) at the time when the pneumatization process starts. Ossification usually denotes the replacement of cartilage or connective tissue by bone. Although pneumatization includes the addition of bony layers to the internal surface of the skull roof, it is the appearance of airfilled cavities within the bone that is the structurally and functionally important morphological change. Passerines are not the only birds to show pneumatized parts of the skull, but they are among the only groups which develop a completely pneumatized skull roof and the only group in which skull pneumatization can be used for ageing live birds. In most non-passerines, the process of pneumatization is completed by the time that the young bird reaches adult size. In passerines, however, skull pneumatization only starts at this moment, i.e. after fledging. This is due to differences in brain development between passerines and non-passerines (Sutter 1943). In non-passerines, the brain grows steadily to its adult volume and skull pneumatization terminates with the attainment of the final brain and body size. In young passerines, the brain goes through a phase of excess weight and volume, after which it shrinks to its adult size by the loss of water. The skull roof remains unpneumatized until the maximum brain volume is attained and pneumatization commences as the brain begins to contract to its adult volume, roughly coincidental with fledging. Consequently, pneumatization continuously fills the gap arising between the unpneumatized skull roof and the shrinking brain surface. The histological differences in the formation of the pneumatized skull roof between passerines and non-passerines have been described by Stork (1972), who was also the first to point out the interrelation of brain development and skull pneumatization described above (Stork 1967). In European passerines, the time required for the formation of the second layer of bone depends on the species and lies between two and eight months. Since the process is generally correlated with the age of a bird, the stage of skull pneumatization may be used to indicate age throughout this period (Jenni & Jenni-Eiermann 1987, section 4.4.3). However, more studies are needed on the amount of individual variation in the progress of pneumatization and possible factors influencing it (e.g. sex, hatching date, environmental factors).
Recognition of skull pneumatization The differences between pneumatized and non-pneumatized areas of the skull roof are easily recognizable on cleaned skull preparations. The unpneumatized, single layered parts (the so-called windows) have the consistency of parchment and are translucent. The pneumatized, double layered parts appear milky white and dotted. The dots are the points of attachment of the tiny bony struts which keep the two layers apart. In live birds, the differences in transparency are less marked, but the contrast between the dotted pneumatized and undotted unpneumatized parts, especially the demarcation line where the two areas meet, is easily visible. The examination of skull pneumatization in live passerines (commonly called skulling) best follows the method of Baird (1963). The bird is held in one hand so that it cannot move its head. The tip of the index finger of the other hand is wetted with water and the crownfeathers of the bird are parted just beside the midline, so as to reveal an unfeathered area of the scalp which serves as a peep-hole. The thin scalp becomes transparent when moistened and can be moved around in every direction, so that a large part of the whole skull can be surveyed. One now looks for the demarcation line between the pneumatized and the non-pneumatized part of the skull. This pneumatization limit contrasts as a white line between the pinkish brain shining through the nonpneumatized skull roof and the less pinkish, dotted, pneumatized parts. In summer the demarcation line generally appears in the occipital region and in the autumn, rather in the more frontal part of the head. If by moving the scalp around, no pneumatization limit is found, either skull pneumatization has not yet started, or is already complete. In the former case the skull roof appears uniformly undotted, in the latter case It is dotted throughout. In autumn (and in summer in very quickly pneumatizing species), one must take care to also scrutinize the foremost regions of the skull roof in order to detect the very last, small windows over the forehead. A strong source of light is essential to easily examine skull pneumatization in live birds. It is important not to manipulate the scalp too much, otherwise it becomes red and loses its transparency. Injuryrelated haemorrhaged parts of the skull appear dark red, with an irregular pattern and should not be mistaken for unpneumatized areas. Skull pneumatization is not always easy to recognize in live birds. It is impossible to see the skull roof of Corvidae and Coccothraustes coccothraustes through the thick scalp or the jaw muscles. Large passerines (e.g. Lanius spp., large Turdus species) have a thick scalp and some species (e.g. Paridae, Remiz and Panurus) a pigmented scalp, and need some experience for successful examination. Birds moulting the headfeathers have an especially well vascularized skin which is therefore less transparent and greatly hinders inspection. Species of the genera Prunella, Erithacus, Acrocephalus, Sylvia, Fringilla, small Carduelis and Emberiza schoenidus after moult are best suited for learning skulling skills. Beginners usually have more problems in holding the skull still while at the same time moving the scalp, than in recognizing the difference between pneumatized and unpneumatized parts. Once one has discovered how to manipulate the bird for inspection and learnt how to recognize the demarcation line between pneumatized and unpneumatized skull parts, the process of skulling soon becomes a matter of routine and takes no more time than weighing the bird.
202
Appendix
Main pattern
Turdus
Parus
Troglodytes Regulus
Hirundo
Sitta
The use of skull pneumatization for ageing
203
Fig. 651. (Opposite] Scoring categories for the pneumatization of the skull roof in passerines (after Winlder 1979). Pneumatized parts (dotted) are indicated on a skull seen from above (see stage 7). Generally pneumatization starts in the occipital region and ends over the forehead. Stage 1 denotes the unpneumatized skull roof or the first evidence of pneumatization in the form of a semi-circle framing the cerebellum. At stage 2, pneumatization has expanded over the whole cerebellum leaving one or two small windows in the centre. In stage 3 about a third, in stage 4 about half and in stage 5 about three quarters of the skull roof are pneumatized. Stage 6 is recognized by one or two small windows remaining over the forehead. Stage 7 denotes the fully pneumatized skull roof. Most species follow the main pattern. Some species show patterns specific of certain genera. Turdus species may follow both the main and the Turdus pattern.
Skull pneumatization scores The process of skull pneumatizarion has been classified into different stages and allotted to various patterns by several authors (e.g. Hogstad 1971, Stewart 1972, Yunick 1979, 1981, Stork & Warncke in Bub 1985, Muller 1987, Pyle etal. 1987, Svensson 1992). For the purpose of this book, we have adopted the scoring system of Winlder (1979). Seven stages are recognized (Fig. 651) according to the proportion of the skull roof pneumatized. However, the time periods between one stage and the next are not necessarily equal between all adjacent pairs of scores and may vary between species. Most species follow the same pneumatization pattern (the main pattern in Fig. 651). For some birds, additional patterns have been described, specific to certain genera.
Age determination by skull pneumatization Birds with incompletely pneumatized skull roofs (stages 1â&#x20AC;&#x201D;6 in Fig. 651) are generally first-year birds. However, some or all adults of certain species never achieve a fully pneumatized skull: Sitta europaea regularly stops pneumatization at stage 6; in Delichon urbica^ Hirundo rustica^ Emberiza citrinella and possibly E. hortulana^ a high percentage of the adults never reach stage 7 (see species accounts). Very exceptionally, adults of other species may retain small unpneumatized windows (stage 6). Birds with a fully pneumatized skull roof can only be determined as adults during the period when none of the first-year birds has yet completed skull pneumatization. Fig. 652 provides data on the progress of skull pneumatization of 46 species and gives the date at which the earliest first-year birds appear with fully pneumatized skulls. As explained in the next section, these data were collected in Switzerland. In other areas, the earliest fully pneumatized first-year birds may appear earlier or later. Since the majority of first-year birds retain unpneumatized parts of the skull well beyond these earliest dates, it is worth checking skull pneumatization until much later in the season so as to identify at least some of the first-year birds, by this method, especially in species in which ageing is difficult by other means. In most species, skull pneumatization is very useful in ageing those individuals in which other characters are ambiguous and is especially recommended as an independent criterion to verify newly discovered ageing criteria after the postjuvenile/postbreeding moult.
collections of the Natural History Museum, Basel (published in Winlder 1979). Skull pneumatization was examined routinely for each individual caught, except when in heavy moult of the head-feathers. The age of first-year birds with fully pneumatized skulls was determined by plumage characters.
Interpretation and relevance of the graphs: The ten-day period (decade) during which the earliest first-year bird with a fully pneumatized skull was found can be read from the lines indicating the range (when it reaches the upper frame of the graph). Consequently, up to this decade birds with fully pneumatized skulls can be determined as adults. Remember that these are from migrating birds in Switzerland. In S Europe, first-year birds will likely complete skull pneumatization earlier due to an earlier breeding season. Apart from providing a guide to age determination by skull pneumatization, the graphs will not be interpreted in detail here. However, it is important to realize that the increase in mean pneumatization score indicated does not reflect the progress of skull pneumatization in an individual bird. The mean pneumatization scores in the graphs usually increase at a considerably slower rate than does the score of an individual bird (Jenni & Jenni-Eiermann 1987, section 4.4.3). In summer, this is probably due to the gradual appearance of later hatched juveniles, which may even cause a slight decrease in the mean score of the population during late summer (e.g. Carduelis flammea). Furthermore, it appears that late-hatched birds migrate later in the season than earlyhatched birds, but apparently at a similar age of life (see section 4.4.3). Consequently, the mean score at sites at which only birds on active migration are caught, may remain more or less stable over several weeks (e.g. Motacilia flava, Luscinia megarhynchos, Hippolais icterina, Emberiza hortulana caught exclusively as migrants at the Alpine pass Col de Bretolet). In most species, the graphs show a stable mean pneumatization score in the summer, an increase before or at the beginning of autumn migration and a plateau thereafter. An interpretation of these patterns is beyond the scope of this book and may be due to the effects discussed above, to the fact that the scores do not represent equal time spans and to a change in the age composition of first-year birds during the season (e.g. sharp increases in mean score may be due to the arrival of early-hatched migrants into a later hatched Alpine population; Winkler 1979).
Explanations of the graphs Material: The graphs show skull pneumatization scores (including score 7) of first-year birds examined at the bird ringing stations mentioned in chapter 6. Additional data are included from earlier years collected on Col de Bretolet in 1972-1974, 1976, 1977 and from other sites in Switzerland on live birds as well as from the
Fig. 652. (Below) Skull pneumatization scores of first-year birds examined in Switzerland. Data are grouped into ten-day periods (decades; see Table 9). The large graphs include values grouped by months. For each period, the mean (circle), mode (dot, most frequent value) and range (line) are indicated.
204
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206 Appendix
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Scientific names with their English, German, French, Italian and Spanish translations Scientific names
English
German
French
Italian
Spanish
Acrocephaius agricola Acrocephalus arundinaceus Acrocephaius dumetorum Acrocephalus melanopogon Acrocephaius paludicola Acrocephaluspalustris Acrocephalus schoenohaenus Acrocephalus scirpaceus Aegithalos caudatus Alauda arvtrmis Anthus campestris Anthus cervinus Anthus pratensis Anthus richardi Anthus spinoletta Anthus trivialis
Paddyfield Warbler Great Reed Warbler Blyth's Reed Warbler Moustached Warbler Aquatic Warbler Marsh Warbler Sedge Warbler Reed Warbler Long-tailed Tit Skylark Tawny Pipit Red-throated Pipit Meadow Pipit Richard's Pipit Water Pipit Tree Pipit
Pel d rohrsanger D rossel rohrsanger Buschrohrsanger Mariskensanger Seggenro h rsanger Sumpfrohrsanger Schilfrohrsanger Teich rohrsanger Schwan7,meise Feldlcrche Brachpieper Rotkehlpieper Wtesenpieper Spornpieper Wasserpieper Baumpieper
Rousserolle isabelle Rousserolle turdoide Rousserolle des buissons Lusciniole a moustaches Phragmite aquatique Rousseroile verderolle Phragmite des joncs Rousserolle effarvatte Mesange a longue queue Alouette des champs Pipit rousseline Pipit a gorge rousse Pipit farlouse Pipit de Richard Pipit spioncelle Pipit des arbres
Cannaiola di Jerdon Cannareccione Cannaioia di Blyth Forapaglie castagnolo Pagliarolo Cannaiola verdognola Forapaglie Cannaiola Codibugnolo Allodola Calandro Pispola golarossa Pispola Calandro maggiore Spioncello Prispolone
Carricero agrfcola Carricero tordal Carricero de Blyth Carricerin real Carricen'n cejudo Carricero poh'glota Carricerin comiin Carricero comiin Mito Alondra comun Bisbita campestre Bisbita gorgirrojo Bisbita comiin Bisbita de Richard Bisbita ribereno alpino Bisbita arboreo
Bombycilla garrulus
Waxwing
Seidenschwanz
Jaseur boreal
Beccofrusone
Ampelis europeo
Calandrella brachydactyla Calandrella rufescens Calcarius lapponicus Carduelis cannabina Carduelis carduelis Carduelis chloris Carduelis flammea Carduelis flavirostris Carduelis hornemanni Carduelis spinus Carpodacus erythrinus Cereotrichas galactotes Certhia brachydactyla Certhia familiaris Cettia cetti Chersophilus duponti Cinclus cinclus Cisticola juncidis Coccothraustes coccothraustes Corvus corax Corvus corone Corvus frugilegus Corvus monedula Cyanopica cyana
Short-toed Lark Lesser Short-toed Lark Lapland Bunting Linnet Goldfinch Greenfinch Redpoll Twite Arctic Redpoll Siskin Scarlet Rosefinch Rufous Bush Robin Short-toed Treecreeper Treecreeper Cetti's Warbler Dupont's Lark Dipper Fan-tailed Warbler Hawfinch Raven Carrion Crow Rook Jackdaw Azure-winged Magpie
Kurzzehenlerche Stummellerche Spornammer Han fling Distelfmk Griinfink Birkenzeisig Berghanfling Polarbirkenzeisig Erlenzeisig Karmingimpel Heckensanger Gartenbaumiaufer Waldbaumlaufer Seidensanger Dupontlerche Wasseramsel Cistensanger Kernbcisser Kolkrabe Rabenkrahe Saatkrahe Dohle Blauelster
Alouette calandrelle Alouette pispolette Bruant lapon Linotte melodieuse Chardonneret elegant Verdier Sizerin flamme Linotte a bee jaune Sizerin blanchatre Tarin des aulnes Roselin cramoisi Agrobate roux Grimpereau des jardins Grimpereau des bois Bouscarle de Cetti Sirli de Dupont Cincle plongeur Cisticole des joncs Grosbec casse-noyaux Grand Corbeau Corneille noire Corbeau freux Choucas des tours Pie bleue
Calandrella Pispoletta Zigolo di Lapponia Fanello Cardeliino Verdone Organctto Fanelio nordico Organetto artico Lucarino Ciuffolotto scarlatto Usignolo d'Africa Rampichino Rampichino alpestre Usignolo di fiume Allodola del Dupont Merlo acquaiolo Beccamoschino Frosone Corvo imperiale Cornacchia Corvo Taccola Gazza azzurra
Terrera comun Terrera marismena Escribano lapon Pardillo comun Jilguero Verderon comun Pardillo sizcn'n Pardillo piquigualdo Pardillo de Hornemann Lugano Camachuelo carminoso Alzacola Agateador comiin Agateador norteno Ruisenor bastardo Alondra de Dupont Mirlo acuatico Buitron Picogordo Cuervo Corneja negra Graja Grajilla Rabilargo
Delichon urbica
House Martin
Mehlschwalbe
Hirondelle de fenetre
Balestruccio
Avion comiin
Emberiza aureola Emberiza bruniceps Emberiza caesia Emberiza cia Emberiza cirlus Emberiza citrinella Emberiza hortulana Emberiza melanocephala Emberiza pusilla Emberiza rustica Emberiza schoeniclus Eremophila alpestris Erithacus rubecula
Yellow-breasted Bunting Red-headed Bunting Cretzschmar's Bunting Rock Bunting Cirl Bunting Yellowhammer Ortolan Bunting Black-headed Bunting Little Bunting Rustic Bunting Reed Bunting Shore Lark Robin
Weidenammer Braunkopfammer Grauortolan Zippammer Zaunammer Goldammer Ortolan Kappenammer Zwergammer Wajdammer Roh rammer Ohrenlerche Rotkehlchen
Bruant aureole Bruant a tete rousse Bruant cendrillard Bruant fou Bruant zizi Bruant jaune Bruant ortolan Bruant melanocephale Bruant nain Bruant rustique Bruant des roseaux Alouette hausse-col Rougegorge familier
Zigolo dal collare Zigolo testa aranciata Ortolano grigio Zigolo muciatto Zigolo nero Zigolo giallo Ortolano Zigolo capinero Zigolo minore Zigolo boschereccio Migliarino Allodola golagialla Petti rosso
Escribano aureolado Escribano carirrojo Escribano ceniciento Escribano montesino Escribano soteno Escribano cerillo Escribano hortelano Escribano cabecinegro Escribano pigmeo Esrcibano riistico Escribano palustre Alondra cornuda Petirrojo
Falco tinnunculus Ficedula albicollis Ficedula hypoleuca Ficedula parva Ficedula semitorquata
Kestrel Collared Flycatcher Pied Flycatcher Red-breasted Flycatcher Semi-collared Flycatcher
Turmfalke Halsbandschnapper Trauerschnapper Zwergschnapper Halbringschnapper
Faucon crecerelle Gobemouche a collier Gobemouche noir Gobemouche nain Gobemouche a demi-collier
Gheppio Balia dal collare Balia nera Pigliamosche pettirosso Balia caucasica
Cerm'caio vulgar Papamoscas collarino Papamoscas cerrojillo Papamoscas papirrojo Papamoscas semicollarino
220
Scientific names with their English, German, French, Italian and Spanish translations
Scientific names
English
German
French
Italian
Spanish
Fringilla coelebs Fringilla montifringilla
Chaffinch Brambling
Buchfink Bergfink
Pinson des arbres Pinson du Nord
Fringuello Peppola
Pinzon vulgar Pinzon real
Galerida cristata Galerida theklae Garrulus glandarius
Crested Lark Thekla Lark Jay
Haubenlerche Theklalerche Eichelhaher
Cochevis huppe Cochevis de Thekla Geai des chenes
Cappellaccia Cappellaccia spagnola Ghiandaia
Cogujada comon Cogujada montesina Arrendajo comun
Hippotais caligata Hippolais icterina Hippolais olivetorum Hippolais pallida Hippolais polyglotta Hirundo daurica Hirundo rustica
Booted Warbler Icterine Warbler Olive-tree Warbler Olivaceous Warbler Melodious Warbler Red-rumped Swallow Swallow
Buschspotter Gelbspotter Olivenspotter Blassspotter Orpheusspotter Rotelschwalbe Rauchschwalbe
Hypolai's russe Hypolais icterine Hypolais des oliviers Hypolais pale Hypolais polyglotte Hirondelle rousseline Hirondelle de cheminee
Canapino asiatico Canapino maggiore Canapino levantino Canapino pallido Canapino Rondine rossiccia Rondine
Zarcero escita Zarcero icterino Zarcero grande Zarcero palido Zarcero comun Golondrina daurica Golondrina comun
Irania gutturalis
White-throated Robin
Weisskehlsanger
Iranie a gorge blanche
Irania
Petirrojo turco
Lamus collurio Red-backed Shrike Neuntoter Pie-grieche ecorcheur Averla piccola Alcaudon dorsirrojo Lanius excubitor Great Grey Shrike Raubwiirger Pie-grieche grise Averla maggiore Alcaudon real Lanius isabellinus Isabelline Shrike Isabellwiirger Pie-grieche isabelle Averla isabellina Alcaudon isabel Lanius minor Lesser Grey Shrike Schwarzstirnwiirger Pie-grieche a poitrine rose Averla cenerina Alcaudon chico Lanius nubicus Masked Shrike Maskenwiirger Pie-grieche masquee Averla mascherata Alcaudon nubico Lanius senator Woodchat Shrike Rotkopfwiirger Pie-grieche a tete rousse Averla capirossa Alcaudon comun Locustella certhiola Pallas's Grasshopper Warbler Streifenschwirl Locustelle de Pallas Locustella del Pallas Buscarla de Pallas Locustella fluviatilis River Warbler Schlagschwirl Locustelle fluviatile Salciaiola fluviatile Buscarla fluvial Locustella lanceolata Lanceolated Warbler Strichelschwirl Locustelle lanceolee Locustella lanceolata Buscarla lanceolada Locustella luscinioides Savi's Warbler Rohrschwirl Locustelle luscinioi'de Salciaiola Buscarla unicolor Locustella naevia Grasshopper Warbler Feldschwirl Locustelle tachetee Forapaglie macchiettato Buscarla pintoja Loxia curvirostra Crossbill Fichtenkreuzschnabel Beccroise des sapins Crociere Piquituerto comun Loxia leucoptera Two-barred Crossbill Bindenkreuzschnabel Beccroise bifascie Crociere fasciato Piquituerto franjeado Loxia pytyopsittacus Parrot Crossbill Kiefernkreuzschnabel Beccroise perroquet Crociere delle pinete Piquituerto lorito Lullula arborea Wood Lark Heidelerche Alouette lulu Tottavilla Totovia Luscinia luscinia Thrush Nightingale Sprosser Rossignol progne Usignolo maggiore Ruisenor ruso Luscinia megarhynchos Nightingale Nachtigall Rossignol philomele Usignolo Ruisenor comun Luscinia svecica Bluethroat Blaukehlchen Gorgebleue a miroir Pettazzurro Pechiazul Melanocorypha calandra Calandra Lark Kalanderlerche Alouette calandre Calandra Calandria Miliaria calandra Corn Bunting Grauammer Bruant proyer Strillozzo Triguero Monticola saxatilis Rock Thrush Steinrotel Merle de Roche Codirossone Roquero rojo Monticola solitarius Blue Rock Thrush Blaumerle Merle bleu Passera solitaria Roquero solitario Montifringilla nivalis Snow Finch Schneefmk Niverolle Fringuello alpino Gordon alpino Motacilla alba White Wagtail Bachstelze Bergeronnette grise Ballerina bianca Lavandera blanca Motacilla cinerea Grey Wagtail Bergstelze Bergeronnette des ruisseaux Ballerina gialla Lavandera cascadena Motacilla citreola Citrine Wagtail Zitronenstelze Bergeronnette citrine Cutrettola testagialla orientale Lavandera cetrina Motacilla flava Yellow Wagtail Schafstelze Bergeronnette printaniere Cutrettola Lavandera boyera Muscicapa striata Spotted Flycatcher Grauschnapper Gobemouche gris PigHamosche Papamoscas gris Nucifraga caryocatactes Numenius arquata
N utcracker Curlew
Tannenhaher Grosser Brachvogel
Cassenoix mouchete Courlis cendre
Nocciolaia Chiurlo maggiore
Cascanueces Zarapito real
Oenanthe deserti Oenanthe hispanica Oenanthe isabellina Oenanthe leucura Oenanthe oenanthe Oenanthepleschanka Oriolus oriolus
Desert Wheatear Black-eared Wheatear Isabelline Wheatear Black Wheatear Wheatear Pied Wheatear Golden Oriole
Wustensteinschmatzer Mittelmeersteinschmatzer Isabellsteinschmatzer Trauersteinschmatzer Steinschmatzer Nonnensteinschmatzer Pirol
Traquet du desert Traquet oreillard Traquet isabelle Traquet rieur Traquet motteux Traquet pie Loriot d'Europe
Monachella del deserto Monachella Culbianco isabellino Monachella nera Culbianco Monachella dorsonero Rigogolo
Collalba desertica Collalba rubia Collalba isabel Collalba negra Collalba gris Collalba pia Oropendola
Panurus biarmicus Pants ater Parus caeruleus Parus cinctus Parus cristatus Parus cyanus Parus lugubris Parus major Parus montanus Paruspalustris Passer domesticus Passer hispanwlensis Passer montanus Perisoreus infaustus Petronia petronia Phoenicurus ochruros Phoenicurusphoenicurus Phylloscopus bonelli Phylloscopus borealis Phylloscopus collybita Phylloscopus sibilatrix Phylloscopus trochiloides Phylloscopus trochilus
Bearded Tit Coal Tit Blue Tit Siberian Tit Crested Tit Azure Tit Sombre Tit Great Tit Willow Tit Marsh Tit House Sparrow Spanish Sparrow Tree Sparrow Siberian Jay Rock Sparrow Black Redstart Redstart Bonelli's Warbler Arctic Warbler ChiffchafF Wood Warbler Greenish Warbler Willow Warbler
Bartmeise Tannenmeise Blaumeise Lapplandrneise Haubenmeise Lasurmeise Trauermeise Kohlmeise Weidenmeise Sumpfmeise Haussperling Weidensperling Feldsperling Ungliickshaher Steinsperling Hausrotschwanz Gartenrotschwanz Berglaubsanger Wanderlaubsanger Zilpzalp WaJdlaubsanger Griinlaubsanger Fitis
Mesange a moustaches Mesange noire Mesange bleue Mesange lapone Mesange huppee Mesange azuree Mesange lugubre Mesange charbonniere Mesange boreale Mesange nonnette Moineau domestique Moineau espagnol Moineau friquet Mesangeai imitateur Moineau soulcie Rougequeue noir Rougequeue a front blanc Pouillot de Bonelli Pouillot boreal Pouillot veloce Pouillot sifBeur Pouillot verdatre Pouillot fitis
Basettino Cincia mora Cinciarella Cincia siberiana Cincia dal ciufFo Cincia azzurra Cincia dalmatina Cinciallegra Cincia bigia alpestre Cincia bigia Passera europea Passera sarda Passera mattugia Ghiandaia siberiana Passera lagia Codirosso spazzacamino Codirosso Lui bianco Lul boreale Lui piccolo Lui verde Lui giallo Lui grosso
Bigotudo Carbonero garrapinos Herrerillo comun Carbonero lapon Herrerillo capuchino Herrerillo cianeo Carbonero liigubre Carbonero comun Carbonero sibilino Carbonero palustre Gorrion comun Gorrion moruno Gorrion molinero Arrendajo funesto Gorrion chillon Colirrojo tizon Colirrojo real Mosquitero papialbo Mosquitero boreal Mosquitero comun Mosquitero silbador Mosquitero troquiloide Mosquitero musical
Scientific names with their English, German, French, Italian and Spanish translations
221
Scientific names
English
German
French
Italian
Spanish
Pica pica Pinicola enucleator Plectrophenax nivalis Prunella collaris Prunella modularis Ptyonoprogne rupestris Pyrrhocorax graculus Pyrrhocoraxpyrrhocorax Pyrrhulapyrrhula
Magpie Pine Grosbeak Snow Bunting Alpine Accentor Dunnock Crag Martin Alpine Chough Chough Bullfinch
Elster Hakengimpel Schneeammer Alpenbraunelle Heckenbraunelle Felsenschwalbe Alpendohle Alpenkrahe Gimpel
Pie bavarde Durbec des sapins Bruant des neiges Accenteur alpin Accenteur mouchet Hirondelle de rochers Chocard a bee jaune Crave a bee rouge Bouvreuil pivoine
Gazza Ciuffolotto delle pinete Zigolo delle nevl Sordone Passera scopaiola Rondine montana Gracchio alpino Gracchio corallino Ciuffolotto
Urraca Camachuelo picogrueso Escribano nival Acentor alpino Acentor comun Avion roquero Chova piquigualda Chova piquirroja Camachuelo comun
Regulus ignicapillus Regulus regulus Remizpendulinus Riparia riparia
Firecrest Goldcrest Penduline Tit Sand Martin
Sommergoldhahnchen Wintergoldhahnchen Beutelmeise Uferschwalbe
Roitelet triple-bandeau Roitelet huppe Mesange remiz Hirondelle de rivage
Fiorrancino Regolo Pendolino Topino
Reyezuelo listado Reyezuelo sencillo Pajaro moscon Avion zapador
Saxicola rubetra Saxicola torquata Serinus citrinella Serinus serinus Sitta europaea Sitta neumayer Sitta whiteheadi Streptopelia senegalensis Sturnus unicolor Sturnus vulgaris Sylvia atricapilla Sylvia borin Sylvia cantillans Sylvia communis Sylvia conspicillata Sylvia curruca Sylvia hortensis Sylvia melanocephala Sylvia melanothorax Sylvia nisoria Sylvia rueppelli Sylvia sarda Sylvia undata
Whinchat Stonechat Citril Finch Serin Nuthatch Rock Nuthatch Corsican Nuthatch Laughing Dove Spotless Starling Starling Blackcap Garden Warbler Subalpine Warbler Whitethroat Spectacled Warbler Lesser Whitethroat Orphean Warbler Sardinian Warbler Cyprus Warbler Barred Warbler Riippel's Warbler Marmora's Warbler Dartford Warbler
Braunkehlchen Schwarzkehlchen Zitronenzeisig Girlitz Kleiber Felsenkleiber Korsenkleiber Palmtaube Einfarbstar Star Monchsgrasmiicke Gartengrasmiicke Weissbartgrasmiicke Dorngrasmiicke Brillengrasmiicke Klappergrasmucke Orpheusgrasmucke Samtkopfgrasmiicke Schuppengrasmucke Sperbergrasmiicke Maskengrasmiicke Sardengrasmiicke Provencegrasmiicke
Traquet tarier Traquet patre Venturon montagnard Serin cini Sittelle torchepot Sittelle des rochers Sittelle corse Tourterelle maillee Etourneau unicolore Etourneau sansonnet Fauvette a tete noire Fauvette des jardins Fauvette passerinette Fauvette grisette Fauvette a lunettes Fauvette babillarde Fauvetre orphee Fauvette melanocephale Fauvette de Chypre Fauvette eperviere Fauvette masquee Fauvette sarde Fauvette pitchou
Stiaccino Saltimpalo Venturone Verzellino Picchio muratore Picchiotto rupestre Picchio muratore corso Tortora delle palme Storno nero Storno Capinera Beccafico Sterpazzolina Sterpazzola Sterpazzola di Sardegna Bigiarella Bigia grossa Occhiocotto Occhiocotto di Cipro Bigia padovana Silvia del Ruppel Magnanina sarda Magnanina
Tarabilla nortena Tarabilla comiin Verderon serrano Verdecillo Trepador azul Trepador rupestre Trepador corso T6rtola del Senegal Estornino negro Estornino pinto Curruca capirotada Curruca mosquitera Curruca carrasquefia Curruca zarcera Curruca tomillera Curruca zarcerilla Curruca mirlona Curruca cabecinegra Curruca ustulada Curruca gavilana Curruca de Ruppell Curruca sarda Curruca rabilarga
Tarsiger cyanurus Tichodroma muraria Troglodytes troglodytes Turdus iliacus Turdus merula Turdus philomelos Turduspilaris Turdus torquatus Turdus viscivorus Vireo griseus
Red-flanked Bluetail Wallcreeper Wren Redwing Blackbird Song Thrush Fieldfare Ring Ouzel Mistle Thrush White-eyed Vireo
Blauschwanz Mauerlaufer Zaunkonig Rotdrossel Amsel Singdrossel Wacholderdrossel Ringdrossel Misreldrossel
Robin a flancs roux Tichodrome Troglodyte Grive mauvis Merle noir Grive musicienne Grive litorne Merle a plastron Grive draine
Codazzurro Picchio muraiolo Scricciolo Tordo sassello Merlo Tordo bottaccio Cesena Merlo dal collare Tordela
Coliazul cejiblanco Treparriscos Chochm Zorzal alirrojo Mirlo comiin Zorzal comiin Zorzal real Mirlo capiblanco Zorzal charlo
Species Index
Figures in bold type refer to species accounts, figures in italics to chapter 5 (general ageing criteria). Acrocephalus agricola 27,59 Acrocephalus arundinaceus* 19, 20, 23,57, 59 Acrocephalus dumetorum 16, 27, 59 Acrocephalus melanopogon 18, 29, 30, 44, 52, 53 Acrocephalus paludicola 19, 20, 39, 45, 55? Acrocephaluspalustris 18,19, 20,23, 26,39,45,47,5V, 57, 59 Acrocephalusschoenobaenus 8, 18,19, 20, 21, 23, 26, 27, 29, 39, 45, 46,
59 Acrocephalus scirpaceus 19,20,30,38,39,45,46,55?, 118-119,205 Aegithalos caudatus 44,5ft 53 Alauda arvensis 44,52, 53 Ammospiza caudacuta 2 Ammospiza maritima 2 Anthus campestris 8, 16, 17, 19, 20, 21, 23, 26, 39, 40, 45, 46, 47, 5ft 55,55?, 66-67 Anthus cervinus 18,23,47,55? Anthuspratensis 15, 16, 17, 18,33, 34,39,55?, 71-72,204 Anthus richardi 14,16, 20, 55 Anthusspinoletta 16, 17, 32, 33, 39,40,45,55?, 73-75, 204 Anthus trivialis 14,15,16,17,18, 19, 24, 33, 39,45,59, 68-70, 204 Bombycilia garrulus 31, 5ft 55 Calandrella brachydactyla 3,53 Calandrella rufescens 53 Calcarius lapponicus 16, 17, 23, 24, 25, 55? Cardueliscannabina 2,31,33,34,36,39,41,43,55,56; 177-179,206 Carduelis carduelis 1, 31, 32, 33,34, 35, 36, 37, 39, 40,41,43,44,55, 171-173,206 Carduelis chloris 14, 30, 31, 32, 33, 34, 35, 36, 37, 39, 40, 41, 42, 43, 44,53, 55, 57, 168-170, 206 Carduelisflammea 4, 14, 15, 24, 25, 31, 39,40,52, 55, 180-181, 203, 207 Carduelisflavirostris 25, 55 Carduelis hornemanni 55 Carduelis spinoides 23 Carduelis spinus 14, 15, 18, 25, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42,43,44,55,173-176,206 Carduelis tristis 3 Carpodacus erythrinus 30, 31, 38, 39, 45, 47,52, 55 Carpodacus mexicanus 43 Cercotrichas galactotes 19,55? Certhia 16 Certhia brachydactyla 35, 43, 55 Certhia familiaris 55 Cettiacetti 8, 18,55? Chersophilus duponti 53 Cinclus cinclus 15, 16, 17, 25, 31,43,52, 55 Cisticolajuncidis 12, 15, 24,25,35,43,44, 52,53 Coccothraustes coccothrausies 31, 39, 40,5ft 53, 55, 189-190,201 Corvus corax 14, 25, 55 Corvus corone 25, 55 Corvusfrugilegus 12, 14, 25, 55
Corvus monedula 55 Cyanopica cyana 32, 35, 36, 37,40,41,43,55 Delichon urbica 17, 19, 20,39,45,55?, 65,203 Emberizaaureola 27, 30, 38, 39,45,47,52, 55? Emberiza bruniceps 45 Emberiza caesia 19, 26, 55, 55? Emberiza da 33,39,53, 55, 193-194,207 Emberiza cirlus 43, 55? Emberiza citrinella 18, 38, 39,53, 55, 191-192,203, 207 Emberiza hortulana 15, 19, 21, 26, 32, 38, 39, 40, 45, 46, 47, 55, 55?, 195-197,203,207 Emberiza melanocephala 45, 55? Emberizapusilla 59 Emberiza rustica 59 Emberiza schoeniclus 12, 17, 18, 25, 31, 32, 33, 34, 38, 39, 40, 41, 43, 55?, 198-199,207 Eremophilaalpestris 44,52, 53 Erithacus rubecula 8, 12,30, 31, 39,40,41,42,43,55, 91-93,204 Falco tinnunculus 4, 5 Ficedulaalbicollis 15,16,19,27,55? Ficedula hypoleuca 2, 15, 16, 18, 19,21,23,24,27,32,38,39,40,41, 45,46,5ft 55,55?, 141-145,205 Ficedula parva 52, 55? Ficedula semitorquata 16, 19,55? Fringilla coelebs 2, 14, 25, 31, 32, 33, 34, 39, 40, 41, 42, 51, 55, 158160,206 Fringilla montifringilla 2, 15, 25, 31, 33, 39, 40, 41, 42, 52, 55, 161162,206 Galerida cristata 53 Galerida theklae 53 Garrulusglandarius 14,33,34, 39,5ft 55, 156-157 Hippolais caligata 19, 27,55? HippoLiisicterina 18, 19,39,52, 119-120,203,205 Hippolais olivetorum 19, 20,55? Hippolais pallida 19,27,52 Hippolais polyglotta 18, 19,55? Hirundo daurica 59 Hirundo rustica 14,16, 19, 20,21, 39,45,46,5ft 55?, 64,203 Icteria virens 43 Irania gutturalis 19 Lanius collurio 16, 18, 19, 21, 22, 31, 35, 39, 40, 45, 46, 47, 51, 59, 154-155 Lanius cristatus 12, 14, 22,46,47 Lanius excubitor 43, 55? Lanius isabellinus 18, 19,20,35,45,46,47, 155 Lanius ludovicianus 47
Species Index
Lanius minor 19, 45, 59 Lanius nubicus 19, 26, 31, 46, 55, 55> Laniussenator 18,19,20,26,27,30,35,36,37,45,46,47,57, 55?, 155 Lanius tigrinus 12, 22, 46 Locustella certhiola 22 Locustella fluviatilis 14, 19, 22, 23,26, 30,35,45,47,51, 57, 59 Locustella lanceolata 22 Locustella lusdnioides 14,15,19,20,22,23,26,39,45,47,55? Locustella naevia 16, 18, 19, 21, 22, 29,55? Loxia curvirostra 5, 8, 11, 12, 17, 35, 36, 38, 41, 43, 44, 53, 55, 182-
187 Loxia leucoptera 55, 184 Loxia pytyopsittacus 55 Lullula arborea 52,53 Luscinia luscinia 16, 17, 19,23,27,55 Luscinia megarhynchos 16, 19, 24, 27, 39,40, 55, 94, 203, 204 Luscinia svecica 4,17,18,19,23,38,39,52,55?, 95 Melanocorypha calandra 53 Miliaria calandra 44,53
Monticola saxatilis 19,31,55? Monticola solitarius 55 Montifringillanivalis 12, 14, 17,18,44,53 Motacilla alba 8, 15, 16, 17, 25, 32, 33, 34, 39,40,41, 43, 45,55?, 8386, 204 Motacilla cinerea 15,16, 17, 32, 33, 34, 39,55?, 80-82,204 Motacilla citreola 59 Motacillaflava 15,16,17,18,19,23,24,25,30,33,34,38,39,40,41, 42,45,47,52,57,59, 76-79, 203, 204 Muscicapastriata 14, 15, 16, 18, 19, 20, 21, 38, 39,40, 46,5ft 51, 57, 55?, 138-140,205 Nectariniajohnstoni 2 Nucifraga caryocatactes 54,55 Numenius arquata 13 Oenanthe deserti 19 Oenanthe hispanica 17,19,45,55? Oenanthe isa bellina 17,19,55? Oenanthe leucura 55 Oenanthe oenanthe 7,14,16,17,19,23, 39, 40,59, 104-106, 204 Oenanthe pleschanka 17, 19,45,55? Oriolus oriolus 16,18,19,21,30,31,40,46,51,57,59,153-154 Panurus biarmicus 25, 30, 31,44,49, 50, 52,53, 201 Parusater 33,39,41,42,55, 146-147, 206 Parus caeruleus 24, 25, 29, 31, 32, 33, 34, 39, 40, 41, 53, 55, 56, 148149,206 Parus cinctus 55 Parus cristatus 5ft 55 Parus cyanus 55 Parus lugubris 55 Parusmajor 12,24,25,31, 32,33,34,39,40,41,42,53, 55, 150-151, 206 Parus montanus 24, 25,5ft 55 Paruspalustris 5ft 55 Passer domesticus 12,13,14,24,25,30, 31,43, 44,53, 54 Passer hispaniolensis 12, 25, 44, 53 Passer montanus 24, 25,44,53 Passerina 47 Pericrocotus divaricatus 12,22 Perisoreus infaustus 55 Petroniapetronia 53 Phoenicurus ochruros 31, 32, 33, 39,40,42,55, 96-98,204 Phoenicurusphoenicurus 18, 19, 24, 25, 32, 39, 40, 41, 45, 52, 55, 99100,204
223
Phylloscopus bonelli 19, 21, 27, 29,30, 37,57 55? Phylloscopus borealis 59 Phylloscopus collybita 15, 16, 17, 18, 25, 29, 30, 32, 33, 34, 37, 39,40, 41,55?, 133-135,205 Phylloscopus sibilatrix 14, 19, 21, 22, 29, 30, 37, 55? Phylloscopus trochiloides 59 Phylloscopus trochilus 12, 15, 19, 22, 23,24, 25, 26, 29, 30, 37, 38, 39, 41,46,52,57,55?, 136-137,205 Pica pica 5ft 55 Pinicola enucleator 24, 55 Plectrophenax nivalis 16, 17, 23, 24, 25,55? Prunella collaris 55 Prunella modularis 12, 16, 25, 31, 32, 33, 39,55, 89-90, 204 Ptyonoprogne rupestris 16, 24, 25, 38, 49, 55 Pyrrhocorax graculus 12, 14,55 Pyrrhocorax pyrrhocorax 12, 14,55 Pyrrhulapyrrhula 12, 14,24,25,31,32,40,41,42,55, 188-189,207 Regulus ignicapillus 16,31,49, 55 Regulus regulus 16,31,49, 55 Remizpendulinus 43,55, 201 Riparia riparia 19,20, 21, 39,45,59, 63 Saxicolarubetra 2,17, 18,19,25,39,45,52,55*, 101-103,204 Saxicola torquata 3,32, 36, 37,40,43,55 Serinus citrinella 15, 24, 33, 39, 40, 41, 42,55, 166-167, 206 Serinusserinus 4,32, 33, 34, 39,40,41,43,55, 163-165, 206 Sim europaea 24, 25,39,43,55, 152,203,206 Sitta neumayer 55 Sitta whiteheadi 55 Streptopelia senegalensis 4 Sturnus unicolor 15, 16,17, 31, 44, 51, 52, 53 Sturnus vulgaris 2,8, 12, 14, 16, 17, 18, 25, 31, 35, 36, 43,44, 45, 51, 52,53,54 Sylvia atricapilLt 3, 18, 29, 31, 32, 33, 34, 37, 39, 40, 41, 42, 43, 49, 57,52,57,55?, 130-132,205 Sylvia borin 8,14, 15,16,17,18,19,20,21, 22,23, 29, 31, 32,37, 39, 40,41,45,46,57,55?, 127-129,205 Sylvia cantillans 3, 16, 17, 19,20,21,23,26,27,36,37,46,47,5755?, 124 Sylvia communis 14, 15, 16, 17, 19, 20, 21, 23, 25, 26, 27, 30, 36, 37, 39,40,45,46,47,55, 57, 55?, 123-126, 205 Sylvia conspicillata 19, 43,44,55? Sylvia curruca 16, 19, 21, 23, 24, 32, 34, 39, 40, 46, 51, 59, 121-122, 205 Sylvia hortensis 19, 21, 26, 27, 35,46,55, 55? Sylvia melanocephala 18, 19, 24, 25, 30, 31, 35, 36, 37, 40, 43,44, 55,
59
Sylvia melanothorax 32, 35, 37,40,43,44,55? Sylvianisoria 14, 15, 16, 17, 19,21,23,26,30,31,38,40,46,47,55, 55?, 124 Sylvia rueppelli 19, 32, 40, 55? Sylvia sarda 18,55? Sylvia undata 18,32,40,43,55? Tarsiger cyanurus 55 Tichodroma muraria 31, 55? Troglodytes troglodytes 7, 18, 33,39,40,42,43,55, 87-88,204 Turdus iliacus 24,25, 39,40,55, 115 Turdus merula 18,31, 33, 39,41,42, 49, 51, 55, 109-110,205 Turdusphilomelos 25, 39, 42,55, 113-114, 205 Turduspilaris 25,39,41,42,55, 111-112,205 Turdus torquatus 16,25,32,39,40,41,55, 107-108,205 Turdus viscivorus 39,55, 116-117 Vireo griseus 43
Explanations
224
Explanations
Schematic wing diagram
For further details see chapters 2 and 6.
Feathers
Schematic representation of the right wing and the right half of the tail. The proportion of individuals which have moulted a given feather or feather tract after completion of moult is indicated by hatchings.
Relationship between the extent of moult in different feather tracts Body-feathers MaC MeC GC CC Al PC T S P R
contour feathers of the body, head and legs marginal covert(s) median covert(s) greater covert(s) carpal covert alula feather(s) primary covert(s) tertial(s) secondary/ies primary/ies rectrix/rectrices or tail-feather(s)
Moult and feather generations juv postj uv postbr prebr
juvenile post] uvenile postbreeding prebreeding
Age classes ly 2y ad
first-year bird(s) (EURING code 3), i.e. fledged in the current calendar year second-year bird(s) (EURING code 5), i.e. fledged in the previous calendar year adult(s), i.e. fledged before the current calendar year (EURING code 4) or before the previous calendar year (EURING code 6),
Summary statistics on the extent of moult The proportion of birds which have moulted a certain number of feathers of a tract after completion of moult is given. If there is no mention of the body-feathers, they are usually all moulted. Within the wing and tail, only the feathers moulted are listed; those not mentioned have not been observed as replaced. For the number of greater coverts moulted, the range, arithmetic mean and mode (most frequent value) are given as well as the proportion of birds which have moulted none or all greater coverts.
The percentage of individuals which have moulted one or more feathers of the various tracts, after completion of moult, is plotted against the number of greater coverts moulted (x-axis). N = sample sizes.
Seasonal variation of moult extent Data are usually grouped into five-day periods (Table 9, p. 62), or, in the case of small sample sizes, into ten-day periods or by month. Mean number of greater coverts moulted. Lines indicate the 10 - 90th percentiles, and thus comprise 80% of the birds.
Skull pneumatization (see also p. 201) Data are grouped into ten-day periods (see Table 9, p. 62). Above the graph: N = sample size. When the line indicating the range reaches score 7, some ly birds have completed skull pneumatization and cannot be distinguished from ad by this method. For details see Appendix.
Explanations
Schematic wing diagram
For farther details see chapters 2 and 6.
Feathers
Schematic representation of the right wing and the right half of the tail. The proportion of individuals which have moulted a given feather or feather tract after completion of moult is indicated by hatchings.
Relationship between the extent of moult in different feather trarts
Body-feathers MaC MeC GC CC Al PC T S P R
contour feathers of the body, head and legs marginal covert(s) median covert(s) greater covert(s) carpal covert alula feather(s) primary covert(s) tertial(s) secondary/ies primary/ies rectrix/rectrices or tail-feather(s)
Moult and feather generations juv postjuv postbr prebr
juvenile postjuvenile postbreeding prebreeding
Age classes ly 2y ad
first-year bird(s) (EURING code 3), i.e. fledged in the current calendar year second-year bird(s) (EURING code 5), i.e. fledged in the previous calendar year adult(s), i.e. fledged before the current calendar year (EURING code 4) or before the previous calendar year (EURING code 6).
Summary statistics on the extent of moult The proportion of birds which have moulted a certain number of feathers of a tract after completion of moult is given. If there is no mention of the body-feathers, they are usually all moulted. Within the wing and tail, only the feathers moulted are listed; those not mentioned have not been observed as replaced. For the number of greater coverts moulted, the range, arithmetic mean and mode (most frequent value) are given as well as the proportion of birds which have moulted none or all greater coverts.
The percentage of individuals which have moulted one or more feathers of the various tracts, after completion of moult, is plotted against the number of greater coverts moulted (x-axis). N = sample sizes.
Seasonal variation of moult extent Data are usually grouped into five-day periods (Table 9, p. 62), or, in the case of small sample sizes, into ten-day periods or by month. Mean number of greater coverts moulted. Lines indicate the 10 - 90th percentiles, and thus comprise 80% of the birds.
Skull pneumatization (see also p. 201) Data are grouped into ten-day periods (see Table 9, p. 62). Above the graph: N = sample size. When the line indicating the range reaches score 7, some ly birds have completed skull pneumatization and cannot be distinguished from ad by this method. For details see Appendix.