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Garganey Spatula querquedula Scientific name definitions

Carles Carboneras and Guy M. Kirwan
Version: 1.0 — Published March 4, 2020
Text last updated December 21, 2014

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Field Identification

37–41 cm; male 260–520 g, female 240–585 g (1); wingspan 58–69 cm. Adult male in breeding plumage readily separated from all other ducks; eclipse male, female and young birds most likely to be confused with abundant Anas crecca, but paler, with longer bill, whiter throat, more distinct dark eyestripe, paler supercilium, greyish forewing, greenish-brown speculum and dark leading edge to wing; in addition, same-age/sex Sibirionetta formosa has more buff on lower face and white loral spot, while Spatula discors has blue (rather than greyish) forewing. Breeding male has white stripe curving from above eye to nape, contrasting with black-brown forehead and crown, golden-brown foreneck flecked white, black-brown mantle to uppertail-coverts, with feathers fringed paler, tail brown-grey, undertail white with dark brown bars and spots, pink-brown breast barred black, vermiculated greyish flanks and white belly; green speculum with white line along front and rear edges, and pale grey blue upperwing-coverts; elongated scapulars striped grey, dark green and black and white; bill lead-grey to black, legs dull grey and eyes brown. Male has female-like eclipse plumage , but is brighter, has whiter throat and belly, and retains more colourful upperwing. Female has duller upperwing, whitish belly and distinctive striped facial pattern ; bill greenish grey, eyes umber-brown and legs olive-grey to grey. Juvenile resembles female but has finely streaked and spotted ventral parts.

Systematics History

Normally placed in Anas; or occasionally monospecific Querquedula. Monotypic.

Subspecies

Monotypic.

Hybridization

Hybrid Records and Media Contributed to eBird

  • Garganey x Northern Shoveler (hybrid) Spatula querquedula x clypeata
  • Garganey x Green-winged Teal (hybrid) Spatula querquedula x Anas crecca

Distribution

Breeds in Palearctic, mostly between 42° N and 65° N. Winters in Africa, India and SE Asia E to New Guinea.

Habitat

Breeds mostly inland , on swampy meadows, flooded fields and shallow freshwater marshes, pools and small lakes with abundant emergent vegetation, including in farmland. Winters in coastal marshes or lagoons of both fresh and brackish water, provided there is some partially submerged and well-developed fringe vegetation (1); also on reservoirs (2, 3), rice paddies (4), sewage farms (4) and at sea, whereas marine, tidal and estuarine habitats are only infrequently used in W Europe (5). Breeds up to at least 1200 m in Europe (1), but has been recorded to c. 2600 m in Ethiopia (6).

Movement

Highly migratory , wintering chiefly in sub-Saharan Africa (mainly from Mauritania and Senegambia E to L Chad, but also from Nile Valley S to E Africa, with small numbers reaching S to Malawi and Zambia), Indian Subcontinent and SE Asia (regularly S to Peninsular Malaysia, but also to Indonesia, e.g. Kalimantan (7, 8), Sulawesi (9) and Sumatra) (10), less regularly N to Mediterranean Europe, even N & W Europe (5) and Kazakhstan (11), with very little site fidelity at this season, e.g. same birds have been recorded wintering in India and Africa in different years (1). Autumn migration mainly late Jul to Oct, peaking in Europe in Aug and early Sept, with first arrivals in Senegal by early Sept and Niger in late Sept, with bulk reaching W Africa in mid Oct, but perhaps earlier to arrive in E Africa, as main passage through Egypt is in Aug and early Sept (5), arriving Kenya in mid Oct to Nov (12). Return passage from Africa commences Feb, with early arrivals in North Sea countries at end of that month, but main northbound passage through Europe in Mar–Apr, arriving in northernmost breeding areas in mid May (5), although birds leave Kenya between late Mar and mid Apr (12). In N India, at Keoladeo National Park, the first migrants typically reach the area between mid and late Aug, and depart between late Apr and mid May (13). Vagrants have reached Botswana (14), South Africa (1), Indian Ocean islands (Seychelles, Reunion and Rodrigues), New Guinea (including New Ireland and New Britain) (15), Cocos I (16) and Christmas I (1). Has also occurred on Cape Verdes (17), Azores, Iceland, Faeroes, Bear I (5), Palau, the Marianas (18), Hawaii and Aleutian Is; also North America (c. 175 records), mainly in spring and autumn, particularly on W coast and in Aleutians (19), but also inland (e.g. in Idaho, Apr–May 1990, in which spring there were also records in California, Colorado, Alberta, Saskatchewan, North Dakota, Virginia, Quebec, New Brunswick and on Prince Edward I) (20) and in E (almost always in spring) (19), with a single record from the Revillagigedo archipelago (Mexico), in 1999 (21). Possibly regular winter visitor in N Australia and on Maldives (22), but in very small numbers.

Diet and Foraging

Aquatic invertebrates (worms, insects and their larvae, crustaceans, molluscs), amphibians, small fish, seeds, roots, tubers and green parts of sedges, grasses and aquatic plants. Some seasonal and age-related variation in diet, with molluscs being more important in spring, supplemented with smaller quantities of insects (ostracods, phyllopods), whereas in summer vegetative parts of aquatic plants (e.g. Ceratophyllum, Najas) become main food source, combined with insects and crustaceans, and by autumn has shifted to plant-dominated diet comprising mainly seeds of pondweeds, smartweeds, sedges and docks (Rumex); in winter, takes mainly wild rice seeds and grasses, while ducklings reliant almost exclusively on animal diet (1). Study in Senegalese winter quarters found that Nymphaea seeds comprised 26% of diet, wild Graminea seeds 39%, Cyperaceae 15%, rice 10% and Characae oogoniums 7% (6). Feeds by dabbling, head dipping and picking from surface; also upends in shallow waters. Mainly a nocturnal feeder, but also by day if undisturbed (1).

Sounds and Vocal Behavior

Readily vocalizes only during breeding season, when male gives harsh rattling  or crackling note (like breaking ice or stick being drawn across railings) during “Burp” display, e.g. “rrar ... rrar ... rrar”, which may be given on water, land or in flight (5), while female utters low quacking note (1), “gack”  , most similar to that of Anas platyrhynchos (5), the tempo of calling increasing just prior to take-off; also gives disjointed series of single “gaeg” notes when inciting male to copulate (6). Male lacks any pure whistles in repertoire (5).

Breeding

Starts Apr/May, with main laying period during latter month (1), although young seen as early as mid May and as late as Jul in England (1), and eggs are laid from second half of Apr in W & C Europe, but mainly early May in S & W Russia (5). Pair-bonds usually commenced in winter, even as early as Sept/Oct, although some females arrive on breeding grounds unpaired; promiscuity unknown (1); natal philopatry apparently low (1). In single pairs or loose groups, with densities of 6–7 pairs/km² recorded in Estonia, but is generally strongly territorial (1); nest (constructed by female) (1) is a depression (20 cm wide by 8–10 cm deep) (1) lined with plant material down and some feathers, on ground among grass or reeds, near water (usually within 20 m, exceptionally up to c. 150 m) (5). Single-brooded (23): no data on replacement clutches and unsuccessful pairs may immediately depart to their moulting grounds (1). Usually 8–11 (23) warm buff or pale straw-coloured eggs (6–14), laid at 24-hour intervals, size 40–50 mm × 30–36 mm, estimated mass 27 g (1); incubation 21–23 days, starting on completion of clutch, by female alone guarded by male (1); hatching synchronous (1); chicks have dark brown down above, pale yellow below, with two dark lines from bill to back of head, one through eye and the other below it (1); fledging c. 35–40 days, tended by female alone (23). In a Latvian study, the most significant predator of nests was American mink (Mustela vison) (24). Sexual maturity at c. 1 year. Survival greater among males than females, with oldest recorded bird 14·5 years old (1).

Not globally threatened (Least Concern). Common to abundant throughout range, with European population estimated at 640,000–1,100,000 pairs in early 1990s (1), of which probably up to 90% were in Russia (numbers there put at 570,000–960,000 pairs) (5). Breeding population in W Europe sometimes stated to be broadly stable despite hunting and habitat destruction in its wintering grounds, but most authors consider that species has declined in this region during last 2–3 decades, as well as in Russia, and large declines have been specifically registered in the Netherlands (1250–1750 pairs) and to lesser extent in Poland (2500–4000 pairs), Lithuania (3000–5000 pairs), Germany (4000 pairs), Estonia (2000 pairs) and Latvia (1000–2000) pairs, whereas the situation in Finland (3000 pairs) and Hungary (1300–1500 pairs) is either stable or fluctuating (25); in countries harbouring fewer than 1000 pairs in early 1990s, Denmark (91–107 pairs in 1989) (5), Moldova (300–500 pairs in 1989) (5), Croatia (600–800 pairs) (5) and Italy (200–300 pairs in 1980s) (5) supported broadly stable populations, while those in Czech Republic (290–600 pairs in 1970s, 100–180 pairs in 1985–1989) (5), Sweden (300–500 pairs in late 1980s) (5), France (230–500 pairs) (5) and Belgium (c. 165 pairs in 1972, 70–105 pairs in 1989/91) (5) were decreasing, and that in the UK (maximum 120 pairs in 1989–2000, though more recent mean is 95 pairs) (26) was either stable or in slight decline (1). Elsewhere within breeding range numbers very poorly known, but up to c. 26,000–29,000 pairs estimated in Ukraine (5), c. 100,000 in E & C Siberia and c. 30,000 in W Siberia (1). Conservation issues during summer include destruction of nests due to early mowing of meadows, increased human disturbance, lead poisoning, botulism during hot weather, drainage and intensive grassland management, and hunting, especially in S Russia, where > 500,000 may be shot annually, Ukraine, France (c. 15,000 per annum) and Poland (1). In Africa, winter population concentrates especially in Niger Basin; 2,000,000 throughout sub-Saharan W Africa in mid 1980s, with another 500,000 in E Africa (of which c. 20,000 in Kenya) (6), whereas by new millenium the W African population had apparently decline to c. 1,500,000 individuals (1); 77,310 in Senegal in partial census in winter 1991 (of which > 60,000 were in Djoudj National Bird Reserve and surrounding wetlands) (27), but more than 90,000 in early 1970s, when up to 200,000 birds were wintering in Mali (6), with 100,000 at L Aleg, S Mauritania, in autumn 1987 (28), > 98,500 in N Nigeria in winter 1995/96 (29, 30) and up to 744,000 birds at the Inner Niger Delta in Jan 2001 (31). No definitive records from Congo (32) and numbers have reportedly declined in Ghana since new millenium (4). Habitat destruction and hunting are principal threats on African wintering grounds. In Israel, 100,000–200,000 in autumn. Only recently recorded for first time in Bhutan (33). Tens of thousands in partial censuses in India and Thailand; also in Sri Lanka, where notable count of 129,000 in c. 2000 ha of lagoons in S of island, in late 1980s. Overall estimates for Asian winter range suggested 250,000 in S Asia and 100,000–1,000,000 in E & SE Asia in late 1990s (1). CITES III in Ghana.

Distribution of the Garganey - Range Map
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  • Migration
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Distribution of the Garganey

Recommended Citation

Carboneras, C. and G. M. Kirwan (2020). Garganey (Spatula querquedula), 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.gargan.01
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