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Technical Factsheet
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17 November 2021

Pristiphora abietina (lesser spruce sawfly)

Identity

Preferred Scientific Name
Pristiphora abietina (Christ, 1791)
Preferred Common Name
lesser spruce sawfly
Other Scientific Names
Lygaeonematus abietina
Lygaeonematus abietinus
Lygaeonematus abietum Hartig 1836
Lygaeonematus pini Retzius
Nematus abietinus Christ 1783
Nematus abietum
Nematus pini Retzius 1783
Pristiphora abietum
Pristiphora pini
International Common Names
English
gregarious spruce sawfly
Spanish
nemato de la picea
French
némate de l'épicéa
Local Common Names
Denmark
bladhveps
granhveps, lille
Finland
kuusenneulaspistiaeinen
Germany
Blattwespe, Kleine Fichten-
Kleine Fichtenblattwespe
Hungary
kis lucfenyo leveldarazs
Italy
nemato dell'abete rosso
tentredine dell'abete rosso
Netherlands
sparrebladwesp
Norway
granbarveps, liten
Poland
zawodnica swierkowa
Slovakia
piliarka smrekova
Sweden
granstekeln, lilla
EPPO code
PRISAB (Pristiphora abietina)

Pictures

Top of a young spruce tree damaged by P. abietina attack.
Damage symptom
Top of a young spruce tree damaged by P. abietina attack.
Institut für Forstentomologie, Forstpathologie, Forstschutz, Vienna
Continuously damaged tree with a lot of adventitious leaders.
Damage symptom
Continuously damaged tree with a lot of adventitious leaders.
Institut für Forstentomologie, Forstpathologie, Forstschutz, Vienna
Swollen bud with needles discoloured by oviposition.
Damage symptom
Swollen bud with needles discoloured by oviposition.
Institut für Forstentomologie, Forstpathologie, Forstschutz, Vienna
Shaggy shoot with numerous larvae of P. abietina.
Larvae
Shaggy shoot with numerous larvae of P. abietina.
Institut für Forstentomologie, Forstpathologie, Forstschutz, Vienna
Female ovipositing into a swollen bud on a tree top.
Female ovipositing
Female ovipositing into a swollen bud on a tree top.
Institut für Forstentomologie, Forstpathologie, Forstschutz, Vienna
Egg pocket with an egg of P. abietina in the discoloured needle.
Egg
Egg pocket with an egg of P. abietina in the discoloured needle.
Institut für Forstentomologie, Forstpathologie, Forstschutz, Vienna
Beauveria bassiana (white muscardine fungus); natural enemy. Cocoon with coremia of Beauveria bassiana, which has killed the larva inside.
Natural enemy
Beauveria bassiana (white muscardine fungus); natural enemy. Cocoon with coremia of Beauveria bassiana, which has killed the larva inside.
©Institut für Forstentomologie, Forstpathologie, Forstschutz, Vienna
Petr Kapitola, Central Institute for Supervising and Testing in Agriculture, bugwood.org
Pristiphora abietina
Petr Kapitola, Central Institute for Supervising and Testing in Agriculture, bugwood.org
Refer to Bugwood: http://www.bugwood.org/ImageUsage.html
Petr Kapitola, Central Institute for Supervising and Testing in Agriculture, bugwood.org
Pristiphora abietina
Petr Kapitola, Central Institute for Supervising and Testing in Agriculture, bugwood.org
Refer to Bugwood: http://www.bugwood.org/ImageUsage.html

Distribution

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Host Plants and Other Plants Affected

Symptoms

Singly infested trees have brown needles in May/June, or the shoots at the top and on sunny parts of the crown are defoliated. Repeated infestations cause dieback of the leaders and a bushy deformation of the crown.

List of Symptoms/Signs

Symptom or signLife stagesSign or diagnosis
Plants/Leaves/external feeding  
Plants/Leaves/necrotic areas  
Plants/Leaves/yellowed or dead  
Plants/Stems/dieback  
Plants/Stems/fasciation  
Plants/Whole plant/external feeding  

Prevention and Control

The widespread establishment of spruce plantations in risky sites has led to several control trials of P. abietina. The short-term control effects are achieved by the use of insecticides, but these effects are often insufficient for a pest that recovers rapidly. The long-term effects of biological control, i.e. settlement of Formica rufa, were not really successful. Ant colonies need a lot of light to persist for many years and an adequate prey supply besides P. abietina larvae, and these conditions are difficult to maintain in pure spruce stands. The best long-term effects were made with the following methods.
Silvicultural Control

Tree species are alternated and pure spruce plantations should not be established on risky sites (Netherer and Führer, 1999). If they are already there, the stands should be converted to another tree composition with a maximum of 30% spruce and a minimum of 70% of other tree species (Wiener, 1995).

Amelioration of a Site

Measures are taken to decompose the raw humus layer by high-thinning of the stand. This raises the pH-value of the soil, regenerates a sufficient nutrient supply, deteriorates the conditions for the sawfly and improves the trees' resistance against attack (Büttner, 1956; Merker and Niechziol, 1957; Niechziol, 1958; Merker, 1962).

Genotype Selection of Trees

Oviposition usually coincides with mid- and later flushing spruce genotypes (Ohnesorge, 1957). However, by growing early flushing trees the stands will only be exposed to a late spring frost.

Chemical Control

This requires a precise forecast of damage in the following spring. Prognosis is carried out in the late autumn or early spring prior to pupation, when the pupal eyes of the pronymphs are visible and maximum cocoon mortality has occurred. The litter and humus horizon of 16 test plots (32 if possible) per stand (each plot is 25 cm x 25 cm), situated in the crown projections of as many trees as possible, are stripped off. Each sample is quantitatively searched for live cocoons. The number of live cocoons, the percentage of live female cocoons (larger than 5.8 mm) and the rate of pronymphs are counted. The critical number (the number of females ready for hatching per m²) varies according to the age class of the spruce stand. Stands that are 40- to 60-years-old have a critical number of 50 to 60 females per m²; stands that are 15- to 25-years-old have a critical number of 15 to 25 females per m²; and younger stands have a critical number of 0.5 to 2 females per m².

In the past, chlorinated hydrocarbons and organophosphorous compounds were used to control defoliators. At present, pyrethroids (e.g. deltamethrin) and chitin-blockers (e.g. diflubenzuron) are used to control P. abietina. As the treatment must coincide with early larval stages, the exact timing of application is necessary. This means that sometimes a second treatment is unavoidable, if oviposition is delayed by unfavourable weather conditions. Non-target organisms are usually spared with the application of chitin-blockers. Insecticide treatments can be performed regardless of birds because they disregard the larvae of P. abietina. The insecticide must hit the upper part of the crowns, therefore application by aircraft is necessary in older stands.

Biological Control

The use of micro-organisms has not been successful. The only organisms used against P. abietina are in the Formica rufa group, which predate on the larvae (Egger, 1989). However, problems with the durability of settling Formica nests within spruce stands make this method questionable and gives it only limited success.

Impact

Short incidences of outbreaks can be tolerated from the point of view of forestry because they only cause low increment losses. However, single heavy infestation can be critical for plantations of Christmas trees. The damage caused in longer epidemics results in considerable deformations of the tree crowns causing a bushy shape and/or long, spear-formed leaders without ramification. The height growth is reduced to zero after some years. Average height increment losses from 1917 to 1934 amounted to 33-40% in the Swiss epidemic area. Losses of volume increment increased to 60-68% within 10 years in the Swiss area (Nägeli, 1936), to 60% in Freiburg, Germany (Niechziol, 1958), and amounted to 7.5 m³/ha after 4 years injury in Carinthia, Austria (Schedl, 1953).

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Published online: 17 November 2021

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English

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