- Stejneger's Scoter
 - Stejneger's Scoter
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 - Stejneger's Scoter
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Stejneger's Scoter Melanitta stejnegeri Scientific name definitions

Josep del Hoyo, Nigel Collar, and Guy M. Kirwan
Version: 1.0 — Published March 4, 2020
Text last updated November 3, 2016

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Field Identification

51–58 cm; male 1020–1437 g, female 957 g (1); wingspan 86–99 cm (2). Large Melanitta. Recognizable in flight  by conspicuous white secondaries and greater coverts that form square wingbar (usually just visible on closed wing). Male  glossy blackish (duller in non-breeding season, with pale-mottled flanks) (3); pale grey-white eye with white mark below it; legs and feet red-pink with blackish webs (1). Female medium to dark brown with paler greyish-brown patches between eyes and bill and adjacent to ear-coverts; bill dull olive-black, dark grey or black, feet dull reddish, and irides brown (1). Juvenile as female, paler on breast with whiter and larger pale head markings; bill may become coloured during early spring, but lacks basal swelling of adult; only assumes adult plumage in second autumn; juvenile male is generally dull brown to black, variably mottled with black on upperparts (especially from Dec onwards) (1). Compared to M. fusca, with which this species and deglandi were both previously considered as conspecific (see Taxonomy comments), stejnegeri is separated mainly by shape and colour of bill (3): male stejnegeri  differs from nominate race in larger bill knob, darker, more orange on upper part and red or reddish purple on lower edge, with amount of black on cutting edges variable (sometimes appears absent) and that at base generally more extensive than nominate fusca (3); male deglandi has olive-brown flanks (feathers with paler fringes and can appear very mottled when faded) (3), while bill characters differ subtly from stejnegeri, with less prominent knob (3): black basal knob bleeds further forward onto distal half of culmen on stejnegeri (this area is whitish in deglandi), rim of distal half of bill has narrow yellow or reddish-orange band on stejnegeri (black on deglandi) and where reddish-coloured area on bill sides meets black in basal half, the border is more often concave or straight in stejnegeri (but usually convex in deglandi) (4). Female/first-year stejnegeri has a slightly taller, more swollen culmen base than deglandi, and the forehead feathering does not extend prominently onto the culmen (unlike deglandi) (4).

Systematics History

Usually treated as a subspecies of M. fusca (with race deglandi) or as subspecies of M. deglandi if latter separated from M. fusca, but here treated as a species in its own right (following recent study (5) ). Male differs from male fusca in its smoother-slanting forehead and steeper (vertically angled) and higher-reaching, sometimes hooked-over bill protuberance (morphometric character gauged at 3); yellow-sided red-centred vs all-yellow upper mandible, former with no black cutting edge (3); feathering around bill protuberance extending forward and down, then cutting away sharply, leaving panel of feathers at base of upper mandible vs cutting back and away, creating no side-panel of feathering (3); greatly increased black on base of upper mandible (so yellow does not extend back so far) (2); longer-tailed subocular eye-patch (ns[1]). Male differs from male deglandi in the same first character (although higher reach of bill protuberance in deglandi reduces score: effect size 3.56, score 2); yellow-sided red-centred vs red-sided yellow-centred upper mandible, former with no black cutting edge (3); flanks all black vs dark brown (2). Monotypic.

Subspecies

Monotypic.

Distribution

Breeds in eastern Asia, from Altai, Russia, to the Kamchatka Peninsula (6), south to Mongolia; locally in northeastern Kazakhstan. Occasional occurrences are reported on the lower Yenisey River to Dudinka, but the limits of the breeding range are likely farther east (7, 8). There is a possible discontinuity in range in the southern part of the Angara area (8). Winters along coasts of Kamchatka, Sea of Okhotsk, and Commander Islands south to Japan, Korea, and eastern China.

Habitat

Breeds around small freshwater bodies of boreal forest and Arctic tundra, sometimes well inland, but in Kazakhstan breeds at 1,760–2,300 m (9). Winters mostly at sea (and juveniles also spend whole of first year at sea) (1), usually in shallower waters of littoral zone, and species is periodically recorded inland elsewhere virtually throughout its range in small numbers at this season.

Movement

Migratory; winters on coasts of NE Asia S to Japan and E China; also inland. Prior to leaving vicinity of breeding grounds, those in E Asia mass off Okhotsk coast with smaller numbers on lakes in Kamchatka and on Sakhalin (1). Migration routes poorly known, but an estimated 140,000 pass Kamchatka in spring, with totals of up to 40,000 per hour (1). In Kazakhstan, where both M. fusca and the present species breed, former occurs on spring passage between mid Apr and late May, and in autumn mid Sept to late Nov, whereas stejnegeri arrives on breeding grounds late May/early Jun and departs late Jul–Oct (9). Records of vagrants in Afghanistan (Jan) and Pakistan (Feb 1988) might pertain to fusca but perhaps to stejnegeri (10). Elsewhere, stejnegeri has been reported as a vagrant in Denmark (Oct 2009, Mar 2010 and Feb–Mar 2011, all presumed the same returning individual) (11), SW Finland (May–Jun 1996, May–Jun 2012) (12, 13), N France (Dec 1886) (14), Iceland (Apr–May 2003) (15), Ireland (Nov 2009, Jan 2010 and Dec 2010–Mar 2011, all same bird) (11), Norway (Jun 2011, Jul–Aug 2015, several in 2016) (13, 16, 17), N Poland (Mar 2007) (11) NW Spain (Dec 2011–Jan 2012) (18) and Sweden (May 2012, May 2014) (19, 13); it has also occurred at least twice in W Alaska (May 2001, Jun 2002) and might even prove to be reasonably regular there (20).

Diet and Foraging

Mainly molluscs; also crustaceans, worms, echinoderms, annelids (1), small fish and, in fresh water, insects and their larvae. Little plant material consumed, principally on breeding grounds, where diet of M. fusca and M. deglandi is dominated by amphipods, caddis fly larvae and crustaceans (1). Winter diet mainly saltwater molluscs, but in Japan feeds mainly on crabs (Pinnixa ratubuni) at depths of 30–40 m. Feeds almost exclusively by diving, propelling themselves using both wings and feet (21), though occasionally also dabbles on surface.

Sounds and Vocal Behavior

Usually silent, like M. fusca and M. deglandi, but mentioned are a whistled “fee-er” by displaying male and a low nasal “aah-er”, while female gives a gruff croaking “kraa-ah kraa-ah kraa” (2).

Breeding

Poorly known compared to M. fusca and M. deglandi. Generally starts May/Jun.  Seasonally monogamous; pairs may defend small territory around nest-site (1). In single pairs or loose groups (e.g. on islands), sometimes in association with gull and tern colonies, in wooded boreal or taiga country (1). Nest is shallow depression poorly lined with surrounding plant matter, and also with down, on ground among vegetation. Single-brooded (1). Usually 6–9 eggs (1), laid at rate of one every 1·5 days (22); creamy buff (1) or yellowish white (23) in colour, size 55·4–72·5 mm × 35·7–49 mm (1); incubation period unknown, by female alone; chicks have dark brown down above, white below up to cheeks, neck-sides and lower throat (1); fledging c. 50–55 days. One instance of apparent parasitism by this species on Aythya fuligula (24).

Not globally threatened (Least Concern). Population probably declining and has been estimated 400,000–700,000 individuals, of which potentially c. 1% winter off NE North Korea (25). In breeding range, decline registered in Kazakhstan, while anecdotal evidence alone also indicates losses, e.g. along Lena R in Yakutia numbers said to have declined by up to ten-fold during 1970s (1), but robust data are especially sparse for this member of the M. fusca complex. Apart from risk of large congregations of birds being affected by oil spills (for example, Melanitta species showed evidence of long-term and increasing negative effects as a result of Alaskan Exxon Valdez disaster) (26), the species is threatened because it feeds at depths of 30–40 m and thus is very prone to being trapped in fishing nets (even discarded fishing gear (27) and lead sinkers (28) can represent lethal hazards). N Pacific populations of this species (and other seaducks) have been shown to be highly susceptible, for short periods, to broad-scale oceanic regime changes, which affect both biological and climatic variables; however, it is presently unknown how these changes negatively impact bird populations, either through reduced survival chances or reproductive failure (29).

Distribution of the Stejneger's Scoter - Range Map
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  • Year-round
  • Migration
  • Breeding
  • Non-Breeding
Distribution of the Stejneger's Scoter

Recommended Citation

del Hoyo, J., N. Collar, and G. M. Kirwan (2020). Stejneger's Scoter (Melanitta stejnegeri), 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.whwsco1.01
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