Bucephala islandicaBarrow's goldeneye

Ge­o­graphic Range

Bar­row’s gold­eneyes (Bu­cephala is­landica) have a dis­con­tin­u­ous dis­tri­b­u­tion that con­sists of three sep­a­rate pop­u­la­tions. Ap­prox­i­mately 150,000 to 200,000 birds are dis­trib­uted west of the North Amer­i­can Rocky Moun­tains in aquatic habi­tats, from Mon­tana to south­east­ern Alaska. There are smaller sep­a­rated pop­u­la­tions con­sist­ing of ap­prox­i­mately 4,500 birds found in north­east­ern North Amer­ica, from the shores of the Gulf of St. Lawrence, ex­tend­ing down­ward into Maine. Smaller res­i­dent pop­u­la­tions con­sist­ing of 2,000 can also be found in Green­land and Ice­land. Oddly, the east­ern and west­ern pop­u­la­tions show lit­tle vari­a­tion and are seem­ingly iden­ti­cal on the At­lantic and Pa­cific coasts al­though the pop­u­la­tions do not share sim­i­lar bound­aries. (Gar­dars­son, 1978; Robert, et al., 2008)

Win­ter­ing areas for west­ern pop­u­la­tions ex­tend from south­east­ern Alaska to cen­tral Cal­i­for­nia, with most win­ter­ing birds found in the San Fran­cisco Bay and other large open water areas of the north­west­ern states. East­ern pop­u­la­tions can be lo­cal­ized in the Gulf of St. Lawrence and parts of the north­east­ern States. (Robert, et al., 2008)

Habi­tat

Dur­ing the breed­ing sea­son, Bar­row’s gold­eneyes are pri­mar­ily as­so­ci­ated with in­ver­te­brate-rich fresh­wa­ter and al­ka­line lakes that are sur­rounded by ma­ture bo­real forests, where tree cav­i­ties can be found for nest­ing. Al­though un­com­mon, mat­ing Bar­row’s Gold­eneyes can be as­so­ci­ated with sub­alpine lakes, beaver ponds, and small sloughs in west­ern in­ter­moun­tain areas. East­ern pop­u­la­tions of Bar­row’s gold­eneyes pre­fer the same con­di­tions, but can be more as­sorted with small fish­less lakes. (Robert, et al., 2008)

Win­ter­ing Bar­row’s gold­eneyes mi­grate to­wards coastal areas and are mainly found in rocky coastal ma­rine and es­tu­ar­ine habi­tats, in­clud­ing bays, in­lets, har­bors and large, in­te­rior lakes and rivers. Pre­fer­ring shal­lower ice-free wa­ters, strong swim­ming Bar­row’s gold­eneyes for­age in areas with strong cur­rents, but seem to pre­fer slow-flow­ing water. (Robert, et al., 2008)

  • Aquatic Biomes
  • lakes and ponds
  • rivers and streams
  • coastal

Phys­i­cal De­scrip­tion

Adult Bar­row’s gold­eneyes are sim­i­lar in ap­pear­ance to com­mon gold­eneyes. They are a chunky-bod­ied, medium-sized div­ing duck, with a large, puffy head and a short neck. Males are slightly larger than fe­males, av­er­ag­ing 48 cm in length, com­pared to 43 cm among fe­males, and weigh 1278 grams, com­pared to 818 grams for fe­males. Breed­ing males have daz­zling plumage, an iri­des­cent pur­plish-black, cres­cent-shaped head, with a sin­gle white patch on each side of the face at the base of the bill and eyes. Their sides, breast, belly, and sec­ondary feath­ers are bright white and their back, wings, and tail are a deep black. These birds also have a se­ries of seven white squares run­ning along the sides of their body. Fe­males have dual-col­ored plumage: with a rich-brown head, grey­ish backs, wings, and tails, and white sides, breasts, and bel­lies. Im­ma­ture or eclipse males re­sem­ble fe­males. Both males and fe­males have a short, tri­an­gu­lar bill. Ma­ture adults of both sexes have bright, deep yel­low irises, hence the com­mon name "gold­en­eye”. Dur­ing flight, their high-speed wings pro­duce a whistling sound. (Gar­rot, 2003)

Bar­row’s gold­eneyes can be con­fused with com­mon gold­eneyes. How­ever, adult male Bar­row’s gold­eneyes have a cres­cent-shaped white patch on the sides of their head, which is oval-shaped in com­mon gold­eneyes, and fewer white sec­ondary feath­ers. Fe­males are more eas­ily con­fused; but fe­male Bar­row’s gold­eneyes have shorter, slop­ing heads and broader bills, which taper abruptly to a nar­rower tip. Hatch­lings of both species are also sim­i­lar in ap­pear­ance. (Gar­rot, 2003)

  • Sexual Dimorphism
  • male larger
  • sexes colored or patterned differently
  • male more colorful
  • Range mass
    480 to 1320 g
    16.92 to 46.52 oz
  • Range length
    43 to 48 cm
    16.93 to 18.90 in
  • Range wingspan
    68.58 to 76.2 cm
    27.00 to 30.00 in

Re­pro­duc­tion

They are gen­er­ally monog­a­mous and form pairs while on win­ter­ing grounds. How­ever, male Bar­row’s gold­eneyes can be con­sid­ered polyg­y­nous. Males, also known as drakes, can form si­mul­ta­ne­ous pair bonds with two fe­males. It is sug­gested that polyg­yny in Bar­row's gold­eneyes is not a com­mon breed­ing strat­egy, but is rather an un­usual oc­cur­rence. Males con­duct an as­sort­ment of phys­i­cal dis­plays and vo­cal­iza­tions dur­ing courtship. These dis­plays are sim­i­lar to the dis­plays of com­mon gold­eneyes. Dis­plays in­clude turn­ing their heads and pulling them back at vary­ing speeds, hold­ing their heads up and swing­ing them back­wards with their bills pointed ver­ti­cally, and lift­ing their head up and down with a straight neck. (Savard, 1985)

It is un­known if pair bonds last over mul­ti­ple years, al­though some re­searchers pro­pose Bar­row’s gold­eneyes pair long-term. Forced cop­u­la­tion is com­mon in wa­ter­fowl; how­ever, it has never been doc­u­mented in Bar­row’s gold­eneyes. Drake Bar­row’s gold­eneyes take sev­eral min­utes be­fore mount­ing a prone fe­male; this delay im­plies a strong bond. (Savard, 1985; Savard, 1986)

Bar­row’s gold­eneyes are sec­ondary cav­ity nesters, they use aban­doned nests con­structed by other species, usu­ally ex­ca­vated by pileated wood­peck­ers and north­ern flick­ers. Their nests are hol­lowed out tree cav­i­ties, typ­i­cally white birch. They also ap­pear to rely on the avail­abil­ity of nat­ural cav­i­ties formed in large, de­cay­ing trees for nest­ing. In re­cent decades, nest­ing fe­males have ben­e­fited from man-made nest boxes. Many fe­male Bar­row's gold­eneyes typ­i­cal do not start breed­ing until the age of three years. When fe­males be­come sex­ual ma­ture, they begin to seek out and se­lect suit­able nest sites, ac­com­pa­nied by males. Once cho­sen, the nest is lined with downy feath­ers from the fe­male’s breasts. (Robert, et al., 2010; Savard, 1985)

  • Breeding interval
    Barrow’s goldeneyes breed yearly, although some individuals do skip occasional years.
  • Breeding season
    These birds breed from late May to early April.
  • Average eggs per season
    9
  • Range time to hatching
    29 to 31 days
  • Range fledging age
    8 to 9 weeks
  • Range time to independence
    56 to 65 days
  • Average age at sexual or reproductive maturity (female)
    3.2 years
  • Average age at sexual or reproductive maturity (male)
    2 years

Fe­male Bar­row’s gold­eneyes usu­ally lay a clutch of around 6 to 12 blue-green or olive-green eggs, which are in­cu­bated for 29 to 31 days. Fe­males may leave the nest oc­ca­sion­ally dur­ing the day to for­age. Young Bar­row’s gold­eneyes are well-de­vel­oped at hatch­ing, and are able to leave the nest within the first day. After using their long tails and sharp claws to climb the inner side of the nest cav­ity, young Bar­row’s gold­eneyes must make the long jump from the nest en­trance to the ground, en­cour­aged by the fe­male call­ing to them from below. Young Bar­row’s gold­eneyes have been known to leap from great heights with­out in­jury be­cause of their puffy down feath­ers, which cush­ion their fall. (Robert, et al., 2010)

  • Parental Investment
  • precocial
  • pre-fertilization
    • provisioning
    • protecting
      • female
  • pre-hatching/birth
    • provisioning
      • female
    • protecting
      • female
  • pre-weaning/fledging
    • provisioning
      • female
    • protecting
      • female

Lifes­pan/Longevity

Bar­row’s gold­eneyes are rather long-lived, with a sin­gle in­di­vid­ual reach­ing 18 years of age. Ac­cord­ing to the USGS, an in­di­vid­ual Bar­row’s gold­en­eye was banded one year after hatch­ing in Alaska in 1965 and killed later in 1979, reach­ing nearly 16 years in age. No ex­ten­sive stud­ies on lifes­pan in cap­tiv­ity have been con­ducted. Sev­eral stud­ies sug­gest that longevity is linked to food avail­abil­ity, sta­ble en­vi­ron­ment, and ab­sence of dis­ease and toxic ma­te­ri­als such as lead and mer­cury. ("Longevity Records Of North Amer­i­can Birds", 2013; Evans, et al., 2002)

  • Range lifespan
    Status: captivity
    18 (high) years
  • Typical lifespan
    Status: wild
    15 (high) years

Be­hav­ior

Bar­row’s gold­eneyes de­vote their time to preen­ing, swim­ming, div­ing, perch­ing, fly­ing, and for­ag­ing, with most of their time al­lo­cated in the water. Their gross mor­phol­ogy is built for div­ing and swim­ming, how­ever, this hin­ders their abil­ity to be­come air­borne quickly. In­stead of spring­ing straight up out of the water into flight, as pud­dle ducks do, Bar­row’s gold­eneyes must run across the water to build up speed be­fore tak­ing off. Their prin­ci­pal day­time ac­tiv­ity is for­ag­ing, com­pris­ing of most of their time. They typ­i­cally for­age in small groups, div­ing syn­chro­nously to search for prey. Their re­main­ing time con­sists of preen­ing and bathing while on the sur­face of the water or on the shore­line. Mod­er­ately so­cial out­side of the breed­ing sea­son, Bar­row’s gold­eneyes can be ob­served in flocks of 5 to 10 and rarely in flocks of more than 50. How­ever, mi­grat­ing flocks gather with other groups into large flocks at rest sites. It is not un­usual for Bar­row’s gold­eneyes to for­age with dif­fer­ent wa­ter­fowl species. Flight is rapid, with strong wing beats. (Beauchamp, 1992)

  • Range territory size
    1800 to 14500 m^2

Home Range

Pop­u­la­tions of Bar­row’s gold­eneyes mi­grate be­tween their sum­mer breed­ing ranges and win­ter­ing grounds. They are often one of the last ducks to leave their sum­mer grounds and win­ter as far north as pos­si­ble in ice-free areas. They can be ag­gres­sive and ter­ri­to­r­ial in the spring. Males de­fend ter­ri­tory, and fe­males de­fend the im­me­di­ate area around the nest-site. Paired drakes de­fend ter­ri­to­ries on their breed­ing ponds until mid-in­cu­ba­tion. The size of a breed­ing ter­ri­tory varies de­pend­ing on the lo­ca­tion but it ranges from 0.18 to 1.45 ha. Many fe­male Bar­row's gold­eneyes re­turn to the same breed­ing lo­ca­tions year after year. In some cases, these birds may also de­fend their win­ter ter­ri­to­ries. (Beauchamp, 1992; Eadie, et al., 2014)

Com­mu­ni­ca­tion and Per­cep­tion

Bar­row’s gold­eneyes are mainly silent, ex­cept in courtship when males gives a short "ka-KAA," and near nests, where fe­male makes short soft "cuc" notes. In flight, their wings pro­duce a whistling sound. Vi­sual sig­nals are also used in courtship and ag­gres­sion. (Gar­rot, 2003)

Food Habits

Bar­row’s gold­eneyes con­sume a va­ri­ety of aquatic or­gan­isms. Their diet con­sists of mus­sels, snails, limpets, crus­taceans, isopods, fish eggs, algae, and vas­cu­lar plants. Their diet likely varies re­gion­ally as well as sea­son­ally. Blue mus­sels are an es­sen­tial food source of Bar­row’s gold­eneyes in the coastal wa­ters of British Co­lum­bia. Dur­ing the spring, fish eggs, such as salmon and her­ring eggs, make up a large por­tion of their diet. Bar­row’s gold­eneyes typ­i­cally hunt for prey in water less than 4 me­ters deep, al­though they may hunt in deeper water. They pre­fer to for­age in open water, al­though they can be fre­quently found along rocky shore­lines in­hab­ited by mus­sels. Prey is swal­lowed while sub­merged under the water. Adults may dive for 10 to 50 sec­onds, while downy young only dab­ble in their first few weeks. In­di­vid­u­als in flocks tend to dive and sur­face in a highly syn­chro­nous fash­ion. Syn­chrony al­lows for groups to main­tain co­he­sion and a watch­ful eye dur­ing for­ag­ing trips. (Beauchamp, 1992; Ver­meer, 1982)

  • Animal Foods
  • fish
  • eggs
  • insects
  • mollusks
  • aquatic crustaceans
  • Plant Foods
  • roots and tubers

Pre­da­tion

Bar­row’s gold­eneyes re­main sus­cep­ti­ble to an as­sort­ment of preda­tors. Most pre­da­tion oc­curs on nest­ing fe­males and hatch­lings. Preda­tors in­clude Amer­i­can black bears, rac­coons, bald ea­gles, hawks, owls, and weasels such as Amer­i­can martens and fish­ers. Large preda­tory fish, like north­ern pike and muskel­lunges may also prey on more vul­ner­a­ble, im­ma­ture hatch­lings. Non-na­tive Eu­ro­pean star­lings also de­stroy eggs in at­tempts to seize nest cav­i­ties. Young Bar­row’s gold­eneyes often es­cape preda­tors by div­ing un­der­wa­ter. (Evans, et al., 2002)

Ecosys­tem Roles

Bar­row’s gold­eneyes com­pete for suit­able nest sites with species like com­mon gold­eneyes, buf­fle­heads, squir­rels, north­ern flick­ers, and in­va­sive species like Eu­ro­pean star­lings. Bar­row’s gold­eneyes also com­pete di­rectly with fish for prey and tend to breed and for­age on fish-free lakes. Sim­i­lar to many other duck species, in­traspe­cific nest par­a­sitism is com­mon. Bar­row’s gold­eneyes are par­tic­u­larly noted as brood par­a­sites. Being a brood par­a­site has sev­eral ben­e­fits. The par­a­sitic par­ent does not have to build its own nest, in­cu­bate eggs, or care for chicks. The host fe­male, whose nest is par­a­sitized, ac­cepts in­tro­duced eggs as her own and raises the par­a­site chicks along­side her own brood. Like many ducks, Bar­row’s gold­eneyes are prone to in­fec­tions by a va­ri­ety of par­a­sites. Ex­ter­nal par­a­sites like leeches, lice, bit­ing mos­qui­toes and flies, fleas, mites, and ticks fre­quently in­fest Bar­row’s gold­eneyes. Bar­row’s gold­eneyes are also sus­cep­ti­ble to bot­u­lism and avian cholera. (Ball­we­ber, 2014; Evans, et al., 2002)

  • Ecosystem Impact
  • disperses seeds
Com­men­sal/Par­a­sitic Species

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Bar­row’s gold­eneyes help reg­u­late pop­u­la­tions of prey species in­clud­ing fish, in­sects, mol­lusks, and crus­taceans. This species of duck is also ac­tively tar­geted by sports­man dur­ing fall and win­ter hunt­ing sea­sons. (Robert, et al., 2008)

  • Positive Impacts
  • food

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

There are no known ad­verse ef­fects of Bar­row’s gold­eneyes on hu­mans.

Con­ser­va­tion Sta­tus

Bar­row’s gold­eneyes are pro­tected under the Canada-U.S. Mi­gra­tory Birds Con­ven­tion and are listed as “least con­cern” on the IUCN Red List. How­ever, the Cana­dian Com­mit­tee on the Sta­tus of En­dan­gered Wildlife as­sessed east­ern pop­u­la­tions and con­sid­ers this species as “Spe­cial con­cern.” The provinces of New­found­land and Labrador list east­ern pop­u­la­tions of Bar­row’s gold­eneyes as “Vul­ner­a­ble”. ("BirdLife In­ter­na­tional", 2014; Robert, et al., 2008)

Pop­u­la­tions of Bar­row’s gold­eneyes seem to be rel­a­tively sta­ble. There are sev­eral threats that are ef­fect­ing Bar­row’s gold­eneyes' sur­vival and re­pro­duc­tive suc­cess. Com­mer­cial forestry is likely a sig­nif­i­cant threat to Bar­row’s gold­eneyes but the most dra­matic im­pact on their sur­vival is a loss of habi­tat. Di­rect threats in­clude de­struc­tion of nests dur­ing har­vest op­er­a­tions and a re­duced num­ber of suit­able po­ten­tial nest sites. Hunt­ing also poses a large threat to Bar­row’s gold­eneyes. In­creased dis­tur­bance from hunters can have detri­men­tal con­se­quences if left un­reg­u­lated. Ad­di­tional threats in­clude acid rain, oil spill con­t­a­m­i­na­tion, human dis­tur­bance, and degra­da­tion of food re­sources from oil ex­plo­ration. (Robert, et al., 2008)

Con­trib­u­tors

Michael Kulin­ski (au­thor), North­ern Michi­gan Uni­ver­sity, Alec Lind­say (ed­i­tor), North­ern Michi­gan Uni­ver­sity, Leila Si­cil­iano Mar­tina (ed­i­tor), An­i­mal Di­ver­sity Web Staff.

Glossary

Nearctic

living in the Nearctic biogeographic province, the northern part of the New World. This includes Greenland, the Canadian Arctic islands, and all of the North American as far south as the highlands of central Mexico.

World Map

Palearctic

living in the northern part of the Old World. In otherwords, Europe and Asia and northern Africa.

World Map

acoustic

uses sound to communicate

bilateral symmetry

having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.

carnivore

an animal that mainly eats meat

chemical

uses smells or other chemicals to communicate

coastal

the nearshore aquatic habitats near a coast, or shoreline.

diurnal
  1. active during the day, 2. lasting for one day.
endothermic

animals that use metabolically generated heat to regulate body temperature independently of ambient temperature. Endothermy is a synapomorphy of the Mammalia, although it may have arisen in a (now extinct) synapsid ancestor; the fossil record does not distinguish these possibilities. Convergent in birds.

estuarine

an area where a freshwater river meets the ocean and tidal influences result in fluctuations in salinity.

food

A substance that provides both nutrients and energy to a living thing.

forest

forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.

freshwater

mainly lives in water that is not salty.

granivore

an animal that mainly eats seeds

herbivore

An animal that eats mainly plants or parts of plants.

holarctic

a distribution that more or less circles the Arctic, so occurring in both the Nearctic and Palearctic biogeographic regions.

World Map

Found in northern North America and northern Europe or Asia.

iteroparous

offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).

migratory

makes seasonal movements between breeding and wintering grounds

molluscivore

eats mollusks, members of Phylum Mollusca

monogamous

Having one mate at a time.

motile

having the capacity to move from one place to another.

natatorial

specialized for swimming

native range

the area in which the animal is naturally found, the region in which it is endemic.

omnivore

an animal that mainly eats all kinds of things, including plants and animals

oviparous

reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.

piscivore

an animal that mainly eats fish

polar

the regions of the earth that surround the north and south poles, from the north pole to 60 degrees north and from the south pole to 60 degrees south.

saltwater or marine

mainly lives in oceans, seas, or other bodies of salt water.

seasonal breeding

breeding is confined to a particular season

sexual

reproduction that includes combining the genetic contribution of two individuals, a male and a female

social

associates with others of its species; forms social groups.

tactile

uses touch to communicate

visual

uses sight to communicate

young precocial

young are relatively well-developed when born

Ref­er­ences

2014. "BirdLife In­ter­na­tional" (On-line). IUCN Red List of Threat­ened Species. Ac­cessed April 21, 2014 at http://​www.​birdlife.​org.

United States Ge­o­log­i­cal Sur­vey. Longevity Records Of North Amer­i­can Birds. 2013.3. Patux­ent Wildlife Re­search Cen­ter: Jo Anna, Lut­merd­ing. 2013. Ac­cessed April 21, 2014 at http://​www.​pwrc.​usgs.​gov/​.

Ball­we­ber, L. 2014. Wa­ter­fowl par­a­sites. Sem­i­nars in Avian and Ex­otic Pet Med­i­cine, 13/4: 197–205.

Beauchamp, G. 1992. Div­ing Be­hav­ior in Surf Scot­ers and Bar­row's Gold­eneyes. The Auk, Vol. 109, No. 4: 819-827. Ac­cessed Jan­u­ary 21, 2014 at http://​www.​jstor.​org/​stable/​4088156.

Car­ney, S. 1992. Species, age and sex iden­ti­fi­ca­tion of ducks using wing plumage. Wash­ing­ton, DC Jamestown, ND: US De­part­ment of the In­te­rior, US Fish and Wildlife Ser­vice. Ac­cessed Jan­u­ary 22, 2014 at http://​www4.​ncsu.​edu/​~cs­de­pern/doc­u­ments/WaterfowlWings.​pdf.

Dunn, J., J. Alder­fer. 2011. Na­tional Ge­o­graphic field Guide to the birds of North Amer­ica. Wash­ing­ton, DC: Ran­dom House Inc.

Eadie, J., J. Savard, M. Mal­lory. 2014. "Bar­row's Gold­en­eye (Bu­cephala is­landica)" (On-line). The Birds of North Amer­ica On­line. Ac­cessed Jan­u­ary 22, 2014 at http://​bna.​birds.​cornell.​edu/​bna/​species/​548/​articles/​introduction.

Evans, M., D. Lank, W. Boyd, C. Fred. 2002. A Com­par­i­son of the Char­ac­ter­is­tics and Fate of Bar­row's Gold­en­eye and Buf­fle­head Nests in Nest Boxes and Nat­ural Cav­i­ties. The Con­dor, 116/1: 610-619. Ac­cessed March 16, 2014 at http://​dx.​doi.​org/​10.​1650/​0010-5422(2002)104[0610:ACOTCA]2.​0.​CO;2.

Gar­dars­son, A. 1978. Dis­tri­b­u­tion and num­bers of the Bar­row’s Gold­en­eye (Bu­cephala is­landica) in Ice­land. Nat­turufraedin­gurinn, 48: 162-191.

Gar­rot, d. 2003. "Sea Duck In­for­ma­tion Se­ries" (On-line). http://​www.​seaduckjv.​org/​. Ac­cessed Jan­u­ary 22, 2014 at http://​seaduckjv.​org/​infoseries/​bago_​sppfactsheet.​pdf.

Lavers, J., J. Thomp­son, C. Paszkowski, . Ankney. 2006. Vari­a­tion in Size and Com­po­si­tion of Buf­fle­head (Bu­cephala al­be­ola) and Bar­row's Gold­en­eye (Bu­cephala is­landica) Eggs. The Wil­son Jour­nal of Or­nithol­ogy, Vol. 118, No. 2: 173-177. Ac­cessed Jan­u­ary 22, 2014 at http://​www.​jstor.​org/​stable/​20455856.

Robert, M., R. Benoit, J. Savard. 2002. Re­la­tion­ship among Breed­ing, Molt­ing, and Win­ter­ing Areas of Male Bar­row's Gold­eneyes (Bu­cephala is­landica) in East­ern North Amer­ica. The Auk, 119: 676-684.

Robert, M., B. Dro­let, J. Savard. 2008. Habi­tat Fea­tures As­so­ci­ated with Bar­row's Gold­en­eye Breed­ing in East­ern Canada. The Wil­son Jour­nal of Or­nithol­ogy, Vol. 120, No. 2: 320-330. Ac­cessed Jan­u­ary 21, 2014 at http://​www.​jstor.​org/​stable/​20456149.

Robert, M., M. Vail­lan­court, P. Dra­peau. 2010. Char­ac­ter­is­tics of nest cav­i­ties of Bar­row's Gold­eneyes in east­ern Canada. Jour­nal of Field Or­nithol­ogy, Vol. 81, No. 3: 287-293. Ac­cessed Jan­u­ary 21, 2014 at http://​www.​jstor.​org/​stable/​3676460.

Savard, J. 1985. Ev­i­dence of Long-Term Pair Bonds in Bar­row's Gold­en­eye (Bu­cephala is­landica). The Auk, Vol. 102, No. 2: 389-391. Ac­cessed Jan­u­ary 21, 2014 at http://​www.​jstor.​org/​stable/​4086785.

Savard, J. 1986. Polyg­yny in Bar­row's Gold­en­eye. The Con­dor, Vol. 88, No. 2: pp. 250-252. Ac­cessed Jan­u­ary 21, 2014 at http://​www.​jstor.​org/​stable/​1368925.

Ver­meer, K. 1982. Food and dis­tri­b­u­tion of three Bu­cephala species in British Co­lum­bia wa­ters. Wild­fowl, 33/33: 22-30. Ac­cessed March 18, 2014 at http://​wildfowl.​wwt.​org.​uk/​index.​php/​wildfowl/​article/​view/​646.

van de We­ter­ing, D., F. Cooke. 2000. Body weight and feather growth of male Bar­row's Gold­en­eye dur­ing wing molt. The Con­dor, Vol. 102, No. 1: 228-231. Ac­cessed Jan­u­ary 21, 2014 at http://​www.​bioone.​org/​doi/​full/​10.​1650/​0010-5422%282000%29102%5B0228%3ABWAFGO %5D2.​0.​CO%3B2.