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Common Shelduck Tadorna tadorna Scientific name definitions

Carles Carboneras and Guy M. Kirwan
Version: 1.0 — Published March 4, 2020
Text last updated August 15, 2016

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Field Identification

58–67 cm (1); male 830–1500 g, female 562–1250 g (1); wingspan 110–133 cm (2). Unmistakable ; appears black and white at distance. Upperwing characteristic in flight with white on coverts , dark primaries and iridescent green secondaries  as in all Tadorna species. Bare parts: bright waxy red bill  with large basal knob  in spring, pink legs and feet, and brown eyes. Female slightly smaller with less prominent knob on bill, narrower breastband, blackish belly band, paler vent and usually some white between bill and eye; in non-breeding plumage is much like eclipse male, but remains paler, with browner head and sometimes has all-white underparts. Juvenile  , which superficially resembles young Alopochen aegyptiaca, has largely white underparts and grey or dull black dorsal parts, lacks chestnut breastband, and has white cheeks  and throat ; bare parts are entirely pinkish grey.

Systematics History

One of least typical Tadorna species. Has been considered a possible link between present genus and Alopochen, but further molecular study required. Hybridization with several species of Tadorna, Alopochen aegyptiaca, Anas platyrhynchos and Somateria mollissima recorded in captivity. Monotypic.

Subspecies

Monotypic.

Hybridization

Hybrid Records and Media Contributed to eBird

  • Ruddy x Common Shelduck (hybrid) Tadorna ferruginea x tadorna
  • Common Shelduck x Wood Duck (hybrid) Tadorna tadorna x Aix sponsa

Distribution

Coastal NW Europe and scattered Mediterranean sites E through C Asia to NE China, and S to Iran and Afghanistan. In winter reaches N of Africa, Iraq, Pakistan, N India, Bangladesh and S China.

Habitat

Favours coastal mudflats and estuaries, generally occurring in salt or brackish water, particularly in Europe, but often intentionally seeking fresh water, as well to drink. In Asia, prefers riverine environments, as well as marshes and lakes, in semi-desert and steppe areas (1). Recorded to 2400 m in Bhutan (3).

Movement

Most northern and inland populations move southwards to winter at lower latitudes, thus many Asian birds move to Caspian basin, and small numbers move as far as N Africa, Iraq (with increasing numbers wintering in Arabia in recent years) (4), Pakistan, N India (S to Orissa and N Maharashtra (5), and where recorded as late as third week of Apr) (6), Bhutan (7), Bangladesh, SE China (Oct–Apr), SW Korea, S Japan (especially Kyushu) and exceptionally Taiwan  (1, 8); vagrant to Myanmar, Indochina (Laos and Vietnam), NW & C Thailand (9) and perhaps even Borneo (Sabah) (10). SE European breeding population merely flock in winter, though may move if weather is especially harsh (2, 1). Generally considered only accidental visitor to Iceland (though has bred), Slovakia, Libya (2), Madeira (Nov 1932) (11) and Canary Is (six records between 1984 and 2004) (12, 11); in recent years, has wandered S to W Africa, with records in Mauritania and Senegal in 1973, then Niger (since 1982), Ghana (Jan 1986, Feb 2005) (13), Mali (since 1993) and Guinea (in 2006), and a total of 28 observations, all between mid Oct and late Feb, involving some 187 birds (14). Vagrant to S Russian Far East (8) and Philippines (15). Even within mainly sedentary populations (e.g. those of Britain and North Sea coasts), some spectacular gatherings at moulting sites, in some cases requiring extensive flights (see Family Text); thus, up to 100,000 gather at Heligoland Bight, on NW German coast, between Jun and Oct, with much smaller numbers gathering on several British estuaries, e.g. Bridgwater Bay, SW England (2000–4000 birds) (16), and on Rhine estuary, in the Netherlands (1). Two records from North America—Newfoundland (Nov 2009) and Massachusetts (Dec 2009)—are not accepted (17).

Diet and Foraging

Mostly aquatic invertebrates (molluscs, insects, crustaceans), with predilection for saltwater snail (Hydrobia ulvae), especially in NW Europe; also some small fish and spawn, worms and plant materials (algae, seeds and grain) (1). Observed predating eggs of Common Coot (Fulica atra) (18). In S Europe and Asia, small crustacea and insect larvae are especially favoured (1), while ducklings are apparently especially partial to Nereis and Corophium; one incubating female contained 11,858 Hydrobia snails, while a bird in Russia had 63,880 chironomid larvae in the stomach contents (1). Forages by digging, scything or dabbling on exposed mud and by head dipping and upending in shallow water up to 40 cm deep (1); young will also dive for food, from first day of life, but this behaviour declines rapidly after c. 2 weeks, in females more swiftly more than males (19). Regularly feeds by night, in line with tidal rhythms, and may spend up to 12 hours per day feeding, at least in winter (20, 1).

Sounds and Vocal Behavior

Especially just before and during breeding season; vocalizations sexually dimorphic  from early age (21), with male  uttering varied whistling notes, especially a soft, clear “whee-chew” that becomes urgent and frequent in presence of perceived danger, while female calls are typically louder and lower-pitched (audible over long distances), and possess a cackling quality, e.g. “gagagagaga...” or “ak-ak-ak-ak...”, at rate of c. 12 notes/second, usually given in flight; both sexes give loud hissing notes when threatened (2); ducklings give high-pitched peeping notes while on move or feeding, or soft trills in close contact (1).

Breeding

Starts Apr/May, with older birds generally returning to breeding grounds first (1). Monogamous, with long-term pair-bonds, although pair members may migrate and moult apart (1). Single-brooded (1). In single pairs or small groups, sometimes nesting as close as 1 m apart (1); nest made of grass, moss or bracken, lined with down, in cavities such as hollow trees (up to 8 m above ground) (1) or 1–3 m down rabbit (Oryctolagus cuniculus) or other burrows, but also under hay bales or in nestboxes, and sometimes within more or less open vegetation (perhaps especially on islands), up to 1 km from water (1); site is chosen by female, who also adds material to nests in open sites (no material is usually added to burrow nests) (1). Usually 8–10 creamy white eggs (3–18 (22), with some intra-specific parastism recorded) (1), laid at 24-hour intervals, size 61–71 mm × 43–50 mm, mass 65·5–92·5 g (1); incubation c. 28–31 days (23), by female alone guarded by male (1); chicks hatch synchronously and have blackish down above and on thighs, white below, with green-grey legs and bill, weigh c. 50 g when one day old (1); fledging c. 45–50 days in nursery areas that are regularly up to 3 km (exceptionally 30 km) (24) from nest-site, although parents may abandon young after 15–20 days to commence their own moult migration, whereupon young will form crèches of up to 100 ducklings guarded by one or more adults (1). One curious instance of apparent adoption of young T. tadorna by adult Eurasian Oystercatcher (Haematopus ostralegus) (25). Most duckling mortality due to poor weather and predation by crows, foxes, skuas (1), Great Black-backed (Larus marinus) and Herring Gulls (L. argentatus) (1); one bizarre record of an adult Aythya fuligula killing a young shelduck (26), while adult shelducks sometimes successfully defend their chicks, exceptionally even killing the would-be predator (27). In successful nests, up to 90% of eggs hatch, but colonial nesters have hatching success of just 25–50%, thus dispersed populations have higher breeding success; 13-year study at Ythan estuary, in NE Scotland, found that 35% of young fledged and each pair fledged on average one young/year (1). Sexual maturity at two (female) or 4–5 years (male). Mean adult annual mortality 20% in one study, with mean life expectancy of 4·5 years and oldest ringed bird was c. 14·5 years old (1).

Not globally threatened (Least Concern). Widespread and fairly abundant, especially in W Palearctic , where numbers have increased and range has expanded during last four decades (e.g. first bred in Latvia in 1973, Lithuania in early 1980s (2), Switzerland in 1998–1999 (28, 29, 30, 31), and has recently colonized Czech Republic) (32), perhaps in part due to decline in hunting and provision of nest-sites (either accidentally or planned) (33, 1), with inland nesting also becoming much more frequent in NW Europe during same period, for example in British Isles (34); currently estimated to number c. 325,000 birds, with British population of c. 50,000 birds (10,600 pairs in 1988–1991), > 1500 pairs in France (and up to 35,000 in winters of 1987–1991, where the Somme Bay represents the most important site) (35, 36), 6000–9000 pairs in the Netherlands, 10,000 pairs in Germany (in mid 1980s), 3000 pairs in Denmark, 2000–5000 pairs in Norway and 8000–12,000 pairs in Sweden (2). Major threat in this part of range is that of potential habitat change, such as plans for barrages on estuaries (37, 1), but local declines have become evident due to conflict with shell fisheries (38). In Israel , has become quite common in winter in recent years, with 100–250 birds, and up to 2650 (1983), with first breeding documented in Jun 2016 (39), while > 13,000 were at Sabkhat al-Jabbul, NW Syria, in Feb 2004 (40). Winters in large numbers in Iran, with 73,564 individuals recorded in 1991 census, whereas largest winter total in neighbouring Turkey is just 5390 birds (22). Partial counts in winter 1991 yielded: 3137 in Bangladesh; 4027 in Pakistan; 12,241 in China; and 2333 in South Korea. Overall wintering populations estimated at 75,000 in Black Sea and Mediterranean region (where perhaps increasing) (2), 80,000 in W Asia, Caspian Sea and Middle East, 25,000–100,000 in C & S Asia, and 100,000–150,000 in E Asia (1). Large concentrations for moult (see Movements) make species potentially vulnerable to disease or natural disasters.

Distribution of the Common Shelduck - Range Map
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  • Year-round
  • Migration
  • Breeding
  • Non-Breeding
Distribution of the Common Shelduck

Recommended Citation

Carboneras, C. and G. M. Kirwan (2020). Common Shelduck (Tadorna tadorna), version 1.0. In Birds of the World (J. del Hoyo, A. Elliott, J. Sargatal, D. A. Christie, and E. de Juana, Editors). Cornell Lab of Ornithology, Ithaca, NY, USA. https://doi.org/10.2173/bow.comshe.01
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