This species has an extremely large range, and hence does not approach the thresholds for Vulnerable under the range size criterion (Extent of Occurrence <20,000 km2 combined with a declining or fluctuating range size, habitat extent/quality, or population size and a small number of locations or severe fragmentation). The population trend appears to be stable, and hence the species does not approach the thresholds for Vulnerable under the population trend criterion (>30% decline over ten years or three generations). The population size is extremely large, and hence does not approach the thresholds for Vulnerable under the population size criterion (<10,000 mature individuals with a continuing decline estimated to be >10% in ten years or three generations, or with a specified population structure). For these reasons the species is evaluated as Least Concern.
Distribution and population
AERC TAC. 2003. AERC TAC Checklist of bird taxa occurring in Western Palearctic region, 15th Draft. Available at: http://www.aerc.eu/DOCS/Bird_taxa_of _the_WP15.xls.
AOU. 1998. Check-list of North American birds. American Ornithologists' Union, Washington, D.C.
Cramp, S.; Perrins, C. M. 1977-1994. Handbook of the birds of Europe, the Middle East and Africa. The birds of the western Palearctic. Oxford University Press, Oxford.
Sibley, C. G.; Monroe, B. L. 1990. Distribution and taxonomy of birds of the world. Yale University Press, New Haven, USA.
Stotz, D. F.; Fitzpatrick, J. W.; Parker, T. A.; Moskovits, D. K. 1996. Neotropical birds: ecology and conservation. University of Chicago Press, Chicago.
The Common Goldeneye ranges across the boreal forests of Scandinavia, eastern Europe, Russia
, northern China
, Alaska and northern USA
. Its wintering range is equally broad, encompassing the coast of northern Europe including inland United Kingdom
, scattered coastal and inland water bodies in south-eastern Europe (e.g. Turkey
) and central Asia, the coasts of eastern China, Korea
and the Kamchatkha Peninsula (Russia), the Pacific coast of Canada and the Alaskan coast and inland USA (del Hoyo et al.
The global population is estimated to number c.2,500,000-4,600,000 individuals (Wetlands International 2006), while national population estimates include: <c.100 breeding pairs and c.50-1,000 wintering individuals in China; c.1,000 wintering individuals in Japan and c.100,000-1 million breeding pairs and c.10,000 wintering individuals in Russia (Brazil 2009).Trend justification
The overall population trend is stable, although some populations have unknown trends (Wetlands International 2006). This species has undergone a small or statistically insignificant increase over the last 40 years in North America (data from Breeding Bird Survey and/or Christmas Bird Count: Butcher and Niven 2007).EcologyBehaviour
Most of this species is fully migratory although it may only travel short distances (Kear 2005b), and certain populations in the north-west of Europe may also be sedentary (del Hoyo et al.
1992). The species breeds from April in solitary pairs (del Hoyo et al.
1992), after which it undertakes short northerly moult migrations to coastal areas, large lakes and rivers (Kear 2005b) to undergo a period of flightless moult lasting 3-4 weeks (males leave for this moult migration first while females are still incubating) (Scott and Rose 1996). Large moult gatherings are common during this period, males arriving at such gatherings in early-June and numbers peaking in late-August when adult females arrive (Scott and Rose 1996). The southward autumn migration begins in late-August with most arriving in the winter quarters by early-December (Scott and Rose 1996). Females tend to migrate further than males (Madge and Burn 1988, Scott and Rose 1996) and juveniles migrate further than adults (Scott and Rose 1996). The return migration to the breeding areas occurs as early as mid-February (Scott and Rose 1996), the species timing its arrival to coincide with the thawing and appearance of open water (Kear 2005b). Non-breeders may also oversummer on wintering grounds (Madge and Burn 1988). The species is gregarious outside of the breeding season (Snow and Perrins 1998, Kear 2005b) usually being observed in small scattered groups (Scott and Rose 1996) or in small flocks on migration (Kear 2005b). Several hundred individuals may roost together (Snow and Perrins 1998) and large flocks often gather to feed at sewage outfalls (del Hoyo et al.
1992) during the winter, although the species rarely occurs in very large flocks (Scott and Rose 1996). Habitat
The species is restricted to water close to the shore and less than 10 m deep (Scott and Rose 1996) (showing a preference for waters 4 m deep) (Snow and Perrins 1998). Breeding
When breeding the species shows a preference for oligotrophic lakes devoid of fish (Kear 2005b) but with abundant invertebrate life (Johnsgard 1978), and requires tree-holes (or artificial nestboxes) for nesting (del Hoyo et al.
1992). Suitable habitats include freshwater lakes, pools, rivers (del Hoyo et al.
1992) and deep marshes (Johnsgard 1978) surrounded by coniferous forest (del Hoyo et al.
The species winters mainly at sea (Scott and Rose 1996) on inshore waters (del Hoyo et al.
1992), shallow bays (Kear 2005b), estuaries (del Hoyo et al.
1992) and coastal lagoons (del Hoyo et al.
1992, Scott and Rose 1996), especially in the vicinity of sewage outfalls (del Hoyo et al.
1992). Further to the south and on migration the species may also frequent large rivers, lakes (Scott and Rose 1996, Kear 2005b) and reservoirs (Scott and Rose 1996). Diet
The diet of the species consists predominantly of aquatic invertebrates such as molluscs, worms, crustaceans, aquatic insects and insect larvae (del Hoyo et al.
1992) (e.g. dragonflies, damsel flies and may flies) (Johnsgard 1978), as well as amphibians, small fish (del Hoyo et al.
1992) and some plant material (mainly in the autumn) such as seeds, roots and the vegetative parts of aquatic plants (del Hoyo et al.
1992). Breeding site
The species nests in hollows of mature trees (del Hoyo et al.
1992) (e.g. aspen, spruce or oak) (Flint et al
. 1984) formed by woodpeckers or by bacterial or fungal heart-rot invasions (Kear 2005b) that have internal cavity diameters of c.20 cm (although the height of the hollow does not seem to be important) (Johnsgard 1978). The species will preferentially nest in trees in open stands near water (Johnsgard 1978, Madge and Burn 1988) or solitary trees on the edges of marshes (Johnsgard 1978), rather than in trees in dense stands (to increase the ease of entry by flying) (Johnsgard 1978). The species will also nest in artificial nestboxes (del Hoyo et al.
1992). Management information
In Scotland, UK the introduction of a sewage treatment scheme in the Firth of Forth (a large marine bay) resulted in a considerable reduction in the abundance of the species, with feeding flocks only remaining at outfalls where sewage continued to be discharged in large quantities (Campbell 1984). It was unclear whether the changes in the species's distribution were due to reductions in the number of food items borne in the sewage or to reductions in aquatic invertebrate abundance as a result of the new treatment system (Campbell 1984). In some areas nestbox erection programmes have been shown to cause significant range expansions and population increases (Dennis 1987, del Hoyo et al.
1992), although an experiment in southern Finland found that even though nestbox provision increased breeding numbers of the species there was a negative density-dependent effect on reproductive output (i.e. the number of fledged young did not increase despite an increase in breeding pairs) (Poysa and Poysa 2002). Nesting habitats in general may also benefit from a more extended rotation of timber harvesting (Kear 2005b).Threats
The species is threatened by wetland degradation and loss in North America and is susceptible to atmospheric acid deposition (e.g. acid rain) throughout a large part of its breeding range (Kear 2005b). The main threat to the species in its wintering range is pollution (e.g. from coastal oil spills or other pollutants from sewage outfalls) (del Hoyo et al.
The species is hunted sustainably in Denmark (Bregnballe et al.
2006) although the influence of hunting on global populations is unknown (Kear 2005b).
Brazil, M. 2009. Birds of East Asia: eastern China, Taiwan, Korea, Japan, eastern Russia. Christopher Helm, London.
Bregnballe, T.; Noer, H.; Christensen, T. K.; Clausen, P.; Asferg, T.; Fox, A. D.; Delany, S. 2006. Sustainable hunting of migratory waterbirds: the Danish approach. In: Boere, G.; Galbraith, C., Stroud, D. (ed.), Waterbirds around the world, pp. 854-860. The Stationary Office, Edinburgh, UK.
Campbell, L. H. 1984. The impact of changes in sewage treatment on seaducks wintering in the Firth of Forth, Scotland. Biological Conservation 28: 173-180.
del Hoyo, J.; Elliot, A.; Sargatal, J. 1992. Handbook of the Birds of the World, vol. 1: Ostrich to Ducks. Lynx Edicions, Barcelona, Spain.
Delany, S.; Scott, D. 2006. Waterbird population estimates. Wetlands International, Wageningen, The Netherlands.
Dennis, R. H. 1987. Boxes for goldeneyes: a success story. RSPB Conservation Review: 85-87.
Flint, V. E.; Boehme, R. L.; Kostin, Y. V.; Kuznetsov, A. A. 1984. A field guide to birds of the USSR. Princeton University Press, Princeton, New Jersey.
Johnsgard, P. A. 1978. Ducks, geese and swans of the World. University of Nebraska Press, Lincoln and London.
Kear, J. 2005. Ducks, geese and swans volume 2: species accounts (Cairina to Mergus). Oxford University Press, Oxford, U.K.
Madge, S.; Burn, H. 1988. Wildfowl. Christopher Helm, London.
Poysa, H.; Poysa, S. 2002. Nest-site limitation and density dependence of reproductive output in the common goldeneye Bucephala clangula: implications for the management of cavity-nesting birds. Journal of Applied Ecology 39: 502-510.
Scott, D. A.; Rose, P. M. 1996. Atlas of Anatidae populations in Africa and western Eurasia. Wetlands International, Wageningen, Netherlands.
Snow, D. W.; Perrins, C. M. 1998. The Birds of the Western Palearctic vol. 1: Non-Passerines. Oxford University Press, Oxford.
Vahatalo, A. V.; Rainio, K.; Lehikoinen, A.; Lehikoinen, E. 2004. Spring arrival of birds depends on the North Atlantic Oscillation. Journal of Avian Biology 35: 210-216.
Further web sources of information
Detailed species account from Birds in Europe: population estimates, trends and conservation status (BirdLife International 2004)
Text account compilers
Ekstrom, J., Butchart, S., Malpas, L., Calvert, R.
IUCN Red List evaluators
Butchart, S., Symes, A.
BirdLife International (2014) Species factsheet: Bucephala clangula. Downloaded from
http://www.birdlife.org on 12/07/2014.
Recommended citation for factsheets for more than one species: BirdLife International (2014) IUCN Red List for birds. Downloaded from
http://www.birdlife.org on 12/07/2014.
This information is based upon, and updates, the information published in BirdLife International (2000)
Threatened birds of the world. Barcelona and Cambridge, UK: Lynx Edicions and BirdLife International, BirdLife International (2004)
Threatened birds of the world 2004 CD-ROM and BirdLife International (2008) Threatened birds of the world 2008 CD-ROM. These sources provide the information for species accounts for the birds on the IUCN Red List.
To provide new information to update this factsheet or to correct any errors, please email BirdLife
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Additional resources for this species