Fulmarus glacialisnorthern fulmar

Ge­o­graphic Range

North­ern ful­mars are found through­out the north­ern At­lantic and Arc­tic oceans in the north­ern hemi­sphere. They occur as far south as Cape Cod, Mass­a­chu­setts in the west­ern At­lantic, the British Isles in the east­ern At­lantic, Japan in the west­ern Pa­cific and Cal­i­for­nia in the east­ern Pa­cific. There are 3 rec­og­nized sub­species: F. g. glacialis in the north­ern­most At­lantic, F. g. audubonii is found in the lower Arc­tic of the north At­lantic, and F. g. rodger­sii is found in the north Pa­cific. (del Hoyo, et al., 1992; Huettmann and Di­a­mond, 2000)

North­ern ful­mars range widely across the At­lantic, with in­di­vid­u­als reg­u­larly trav­el­ing be­tween North Amer­ica and Britain, in­clud­ing im­ma­ture in­di­vid­u­als. In the west­ern At­lantic, most north­ern ful­mars in 11 large colonies above 65 de­grees North lat­i­tude in east­ern Canada. Ad­di­tional breed­ing colonies are found in Green­land, New­found­land, and Labrador. Con­cen­tra­tions of north­ern ful­mars occur around New­found­land in early spring and some ev­i­dence sug­gests a gen­eral north­wards move­ment in pop­u­la­tions be­tween May and July. Fledg­lings dis­perse south­wards rapidly from breed­ing colonies in Sep­tem­ber and Oc­to­ber. In win­ter the ma­jor­ity of north­ern ful­mars occur in off­shore wa­ters and are rarely ob­served. (Huettmann and Di­a­mond, 2000)

Habi­tat

North­ern ful­mars are found in ocean wa­ters over con­ti­nen­tal shelves. They are found from the pack ice of Arc­tic wa­ters to tem­per­ate wa­ters. They seem to pre­fer shelf break habi­tats (the area where the con­ti­nen­tal shelf be­gins to de­scend to­wards the sea floor) or areas over the con­ti­nen­tal slope. They are rarely seen more than 100 km from shore. They breed on rocky cliffs and is­lands up to 1 km in­land, but typ­i­cally close to the water or coastal. They have oc­ca­sion­ally been re­ported nest­ing on human struc­tures, like houses in coastal areas. (del Hoyo, et al., 1992; Hatch and Net­tle­ship, 1998)

Phys­i­cal De­scrip­tion

There are 4 color morphs of north­ern ful­mars: very dark, dark, light, and very light. Color morphs seem to dif­fer in their dis­tri­b­u­tion dur­ing the breed­ing sea­son and in the tim­ing of their molt. The 3 rec­og­nized sub­species are dis­tin­guished by dif­fer­ences in bill length and thick­ness and the pro­por­tion of the dif­fer­ent color morphs, al­though the sub­species do have in­di­vid­u­als of mul­ti­ple color morphs gen­er­ally. In­di­vid­u­als of dif­fer­ent color morphs seem to mate in­dis­crim­i­nantly, al­though breed­ing colonies tend to be made up mainly of a sin­gle color morph. Im­ma­ture in­di­vid­u­als can­not be dis­tin­guished from adults. Most molt­ing oc­curs in July. Molt­ing seems to make some pop­u­la­tions un­able to fly, but not oth­ers. Males are slightly larger, on av­er­age 835 g whereas fe­males av­er­age 700 g (range of masses is 450 to 1000 g). The sexes are sim­i­lar in over­all ap­pear­ance. North­ern ful­mars are from 45 to 50 cm long with wingspans of 102 to 112 cm. (del Hoyo, et al., 1992; Hatch and Net­tle­ship, 1998; Huettmann and Di­a­mond, 2000)

North­ern ful­mars have thick, yel­low to gray bills with darker areas over the "tubes." Their legs and feet are flesh-col­ored to gray. Dark color morphs are more com­mon in the south­ern por­tions of their range in the At­lantic and the north­ern por­tions of their range in the Pa­cific. Light color morphs are more com­mon in the north­ern por­tion of the range in the Pa­cific. At­lantic pop­u­la­tions tend to have ro­bust bills and are al­most ex­clu­sively light color morphs, whereas Pa­cific pop­u­la­tions have bills that are more slen­der and ex­hibit the full range of color vari­a­tion. Light morphs are uni­formly pale, with head, neck, and ven­tral sur­faces white and with their backs and wings being gray. Dark morphs are uni­formly dark gray. Nearly all in­di­vid­u­als of any color morph have a light to white patch on the dor­sal sur­face of their wings formed by the ex­posed lighter por­tion of their pri­maries, this is only lack­ing in the dark­est of in­di­vid­u­als. In­di­vid­u­als can vary be­tween the very dark ("dou­ble dark") and light ("dou­ble light") morphs de­scribed above. Vari­a­tion is more of less con­tin­u­ous, but is di­vided into 4 morph cat­e­gories for con­ve­nience. (Hatch and Net­tle­ship, 1998)

North­ern ful­mars can be con­fused with pink-footed shear­wa­ters (Puffi­nus cre­ato­pus) or flesh-footed shear­wa­ters (Puffi­nus carneipes), but can be dis­tin­guished by their thick, rounded heads and stubby bills. (Hatch and Net­tle­ship, 1998)

  • Sexual Dimorphism
  • male larger
  • Range mass
    450 to 1000 g
    15.86 to 35.24 oz
  • Average mass
    700 to 835 g
    oz
  • Range length
    45 to 50 cm
    17.72 to 19.69 in
  • Range wingspan
    102 to 112 cm
    40.16 to 44.09 in

Re­pro­duc­tion

North­ern ful­mars are monog­a­mous and re­join their mates each year at the same nest site for breed­ing. If an in­di­vid­ual's mate dies, they will mate with a young, in­ex­pe­ri­enced mate fol­low­ing year, but at the same nest site. Males and fe­males as­so­ci­ate at the nest­ing colony for a few weeks be­fore they lay an egg. They cop­u­late fre­quently, then both de­part to for­age dur­ing the pre-lay­ing phase. (Hatch and Net­tle­ship, 1998)

Dur­ing the pre-lay­ing pe­riod, fe­males store sperm in their re­pro­duc­tive tract and begin the process of yolk for­ma­tion, which takes about 23 days. After yolk for­ma­tion, fe­males ovu­late, the egg is fer­til­ized, and the fe­male re­turns to the colony and lays her egg within a few hours of ar­rival. Egg-lay­ing oc­curs about 3 weeks after breed­ing. (Hatch and Net­tle­ship, 1998)

North­ern ful­mars begin to breed in April and lay their eggs in late May to early June in large colonies on ledges and among rocks. They may also nest in areas with more soil and veg­e­ta­tion than other seabirds and will even nest on build­ings and walls. Nests are fairly sim­ple scrapes, some­times lined with bits of veg­e­ta­tion. From 80 to 99% of nests are re-used by at least 1 mem­ber of the orig­i­nal pair each year. Fe­males lay a sin­gle, white egg and in­cu­ba­tion lasts for 47 to 53 days. The process of hatch­ing takes from 4 to 5 days. Young fledge at 49 to 58 days in early Sep­tem­ber, with the last young north­ern ful­mars leav­ing their natal sites by early Oc­to­ber. Sex­ual ma­tu­rity is not reached until 5 to 20 years old (av­er­age 8 years in males, 12 years in fe­males). (del Hoyo, et al., 1992; Hatch and Net­tle­ship, 1998)

  • Breeding interval
    Northern fulmars breed once yearly.
  • Breeding season
    Breeding occurs in the late spring and early summer, beginning in May.
  • Range eggs per season
    1 to 1
  • Average eggs per season
    1
    AnAge
  • Range time to hatching
    47 to 53 days
  • Range fledging age
    49 to 58 days
  • Average fledging age
    53 days
  • Range age at sexual or reproductive maturity (female)
    5 to 20 years
  • Average age at sexual or reproductive maturity (female)
    12 years
  • Range age at sexual or reproductive maturity (male)
    5 to 20 years
  • Average age at sexual or reproductive maturity (male)
    8 years

Both par­ents in­cu­bate the eggs, stay­ing on the nest for from 1 to 11 (av­er­age 4.6) days until re­lieved by the other par­ent. Males often take par­tic­u­larly long in­cu­ba­tion shifts at the be­gin­ning of in­cu­ba­tion, pre­sum­ably to allow the fe­male to re­cover from lay­ing the egg. Young hatch with a light cov­er­ing of down and are closely tended by par­ents for 10 to 16 days after hatch­ing, after which par­ents pri­mar­ily visit the nest to feed their young. They are able to ther­moreg­u­late at 3 to 6 days old. Par­ents feed their young by re­gur­gi­ta­tion in re­sponse to the chick's food beg­ging call. Young fledge at 49 to 58 (av­er­age 53) days old, about 4 to 5 days after the par­ents have stopped feed­ing them. Young fledge at 115 to 119% of adult body mass. (del Hoyo, et al., 1992; Hatch and Net­tle­ship, 1998)

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

Lifes­pan/Longevity

North­ern ful­mars have ex­cep­tion­ally long lifes­pans. Av­er­age adult life ex­pectancy is es­ti­mated at 31.8 years. Birds have been re­ported breed­ing at over 50 years old. An­nual sur­vival rates are ap­prox­i­mately 0.988 for adults. Most mor­tal­ity is dur­ing the egg and early hatch­ling phase. (del Hoyo, et al., 1992; Hatch and Net­tle­ship, 1998)

  • Typical lifespan
    Status: wild
    50 (high) years
  • Average lifespan
    Status: wild
    31.8 years

Be­hav­ior

North­ern ful­mars for­age both dur­ing the day and at night, al­though much for­ag­ing may occur at night. They are found in colo­nial nest­ing colonies dur­ing the breed­ing sea­son. North­ern­most, Arc­tic pop­u­la­tions are mi­gra­tory, mov­ing south­wards as the polar ice ex­pands in win­ter. They are ab­sent from their north­ern ranges from No­vem­ber to Feb­ru­ary, in gen­eral. All other pop­u­la­tions are more no­madic or dis­per­sive, rang­ing widely in search of good for­ag­ing op­por­tu­ni­ties out­side of the breed­ing sea­son and dis­pers­ing from breed­ing colonies to pelagic for­ag­ing areas at the end of the sea­son. Young north­ern ful­mars range more widely than adults and often cross oceans. Dur­ing the breed­ing sea­son in­di­vid­u­als spend about 39% of their time at the colony and 61% of their time for­ag­ing. They spend more time for­ag­ing dur­ing the pre-lay­ing pe­riod. (del Hoyo, et al., 1992; Hatch and Net­tle­ship, 1998)

North­ern ful­mars fly in a man­ner typ­i­cal of the fam­ily (Pro­cel­lari­idae), with stuff wing beats and glid­ing. They tend to fly close to the water. They also soar and use up­wellings of air to sup­port aer­ial ma­neu­vers near cliff colonies. Av­er­age air speed in flight has been cal­cu­lated at 13 m/s (47 km/h). North­ern ful­mars are buoy­ant on the water and spend a fair amount of time preen­ing. They bathe with en­thu­si­asm, some­times even be­com­ing com­pletely soaked and un­able to fly for some time after bathing. (Hatch and Net­tle­ship, 1998)

  • Average territory size
    1 m^2

Home Range

Home range sizes for north­ern ful­mars are not re­ported. They de­fend small nest­ing areas (about 1 m around the nest) at breed­ing colonies and will fight with other birds, al­though rarely. They will also use oil-spit­ting to de­fend their nest­ing site. Mean dis­tance to neigh­bor­ing nests av­er­aged 1.6 m in one study. (Hatch and Net­tle­ship, 1998)

Com­mu­ni­ca­tion and Per­cep­tion

North­ern ful­mars are one of the few species of birds with a well-de­vel­oped sense of smell. They may use ol­fac­tion to de­tect and find prey and can be at­tracted to areas by fish oil smells. Sim­i­lar to other pe­trels and shear­wa­ters, they emit a strong, musky odor. In­di­vid­u­als emit this odor when han­dled and colonies and flocks are eas­ily de­tected by their smell. Birds some­times en­gage in al­lo­preen­ing upon re­turn­ing to breed­ing colonies. (Hatch and Net­tle­ship, 1998)

North­ern ful­mar vo­cal­iza­tions have been de­scribed as "cack­ling" or "bray­ing" at var­i­ous speeds. These vo­cal­iza­tions are used dur­ing courtship, at ap­proaches to nest­ing colonies, and in ag­gres­sion against in­trud­ers. They make other calls as well, de­scribed as grunts, mew­ing, and spit­ting, which warns a threat that these birds are about to spit stom­ach oil at them, a de­fen­sive mech­a­nism. Hatch­lings use a food-beg­ging call that stim­u­lates par­ents to re­gur­gi­tate. (Hatch and Net­tle­ship, 1998)

They also use a va­ri­ety of vi­sual dis­plays in ag­gres­sive en­coun­ters, in­clud­ing rais­ing their wings, rush­ing at other birds, and push­ing their breasts against the other bird. They also use their spit­ting call and oil spit­ting in ag­gres­sive en­coun­ters. (Hatch and Net­tle­ship, 1998)

Food Habits

North­ern ful­mars eat fish, squid, and large zoo­plank­ton such as am­phipods (Thysa­noessa, Hy­pe­ria, Gam­marus, and Themisto species). They are op­por­tunis­tic feed­ers and also take dis­carded fish and car­rion, such as whale, wal­rus, and seal blub­ber. They eat a wide va­ri­ety of prey, but seem to pre­fer fish with high fat con­tent. They drink sea­wa­ter. They cap­ture prey mainly at the sur­face, but will oc­ca­sion­ally dive as well. North­ern ful­mars often ac­com­pany fish­ing fleets, form­ing large ag­gre­ga­tions to take ad­van­tage of fish waste. They are one of the few bird species with a well-de­vel­oped sense of smell and are thought to use ol­fac­tion to de­tect prey. They tend to for­age at ma­rine up­wellings that cause tem­po­rary con­cen­tra­tions of large zoo­plank­ton, in­clud­ing areas near ice sheets or up­welling as­so­ci­ated with feed­ing gray whales (Es­chric­tius ro­bus­tus) or trawl­ing op­er­a­tions. North­ern ful­mars travel widely in search of food. Dur­ing the breed­ing sea­son in­di­vid­ual leave the colony on for­ag­ing trips of 4 to 5 days that may take them up to 460 km from the colony, al­though most for­ag­ing is within 100 km of the colony. (del Hoyo, et al., 1992; Hatch and Net­tle­ship, 1998)

Pre­da­tion

North­ern ful­mars are preyed on by red foxes (Vulpes vulpes) and Arc­tic foxes (Vulpes lago­pus) at breed­ing colonies. Other in­tro­duced preda­tors in­clude ground squir­rels (Sper­mophilus) and rats (Rat­tus norvegi­cus). North­ern ful­mars are not sus­cep­ti­ble to these ter­res­trial preda­tors, ex­cept at breed­ing colonies. They will spit a foul smelling oil at preda­tors when threat­ened. (del Hoyo, et al., 1992; Hatch and Net­tle­ship, 1998)

Ecosys­tem Roles

North­ern ful­mars are im­por­tant preda­tors and scav­engers in arc­tic and tem­per­ate pelagic wa­ters. They occur in large breed­ing colonies with other cliff-nest­ing seabirds, in­clud­ing mur­res (Uria), kit­ti­wakes (Rissa), and cor­morants (Pha­lacro­co­rax). They may use areas of breed­ing is­lands with more veg­e­ta­tion and soil ac­cu­mu­la­tion than these other species. They feed on large zoo­plank­ton brought to the sur­face by feed­ing gray whales (Es­chric­tius ro­bus­tus) and are often found in close as­so­ci­a­tion with black-legged kit­ti­wakes (Rissa tri­dactyla) in arc­tic wa­ters. (Hatch and Net­tle­ship, 1998)

North­ern ful­mars are sus­cep­ti­ble to var­i­ous dis­eases, in­clud­ing viral or­nitho­sis, which can be trans­mit­ted to hu­mans, and shell­fish paral­y­sis. Ec­topar­a­sites re­ported are chew­ing lice (Pro­cel­la­r­iphaga bre­v­i­fim­bi­ata, Sae­mu­ndsso­nia oc­ci­den­talis, and Per­ineus ni­grolim­batus), en­dopar­a­sites re­ported are ne­ma­todes (Ste­gopho­rus stel­lae­po­laris). (Hatch and Net­tle­ship, 1998)

Mu­tu­al­ist Species
Com­men­sal/Par­a­sitic Species
  • chew­ing lice (Pro­cel­la­r­iphaga bre­v­i­fim­bi­ata)
  • chew­ing lice (Sae­mu­ndsso­nia oc­ci­den­talis)
  • chew­ing lice (Per­ineus ni­grolim­batus)
  • ne­ma­todes (Ste­gopho­rus stel­lae­po­laris)

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

North­ern ful­mars have been his­tor­i­cally col­lected for food at nest­ing colonies. (Hatch and Net­tle­ship, 1998)

  • Positive Impacts
  • food

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

There are no ad­verse ef­fects of north­ern ful­mars on hu­mans.

Con­ser­va­tion Sta­tus

North­ern ful­mars have a large range and large pop­u­la­tion sizes, they are con­sid­ered "least con­cern" by the IUCN. North­ern ful­mar pop­u­la­tions have in­creased dra­mat­i­cally in the north­ern At­lantic and ex­panded their range in the last 2 cen­turies, pos­si­bly as a re­sult of greater food avail­abil­ity from fish dis­cards from com­mer­cial fish­ing op­er­a­tions. They were once heav­ily ex­ploited at colonies for food, but are not gen­er­ally taken for food cur­rently. They may be threat­ened by coastal pol­lu­tion near breed­ing colonies and likely suf­fer mor­tal­ity as­so­ci­ated with en­tan­gle­ment in fish­ing gear. (del Hoyo, et al., 1992; Hatch and Net­tle­ship, 1998)

Other Com­ments

Ful­marus glacialis may be most closely re­lated to Antarc­tic ful­mars (Ful­marus glacialoides). (Hatch and Net­tle­ship, 1998)

Con­trib­u­tors

Tanya Dewey (au­thor), An­i­mal Di­ver­sity Web.

Glossary

Arctic Ocean

the body of water between Europe, Asia, and North America which occurs mostly north of the Arctic circle.

Atlantic Ocean

the body of water between Africa, Europe, the southern ocean (above 60 degrees south latitude), and the western hemisphere. It is the second largest ocean in the world after the Pacific Ocean.

World Map

Pacific Ocean

body of water between the southern ocean (above 60 degrees south latitude), Australia, Asia, and the western hemisphere. This is the world's largest ocean, covering about 28% of the world's surface.

World Map

acoustic

uses sound to communicate

altricial

young are born in a relatively underdeveloped state; they are unable to feed or care for themselves or locomote independently for a period of time after birth/hatching. In birds, naked and helpless after hatching.

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

carrion

flesh of dead animals.

chemical

uses smells or other chemicals to communicate

coastal

the nearshore aquatic habitats near a coast, or shoreline.

colonial

used loosely to describe any group of organisms living together or in close proximity to each other - for example nesting shorebirds that live in large colonies. More specifically refers to a group of organisms in which members act as specialized subunits (a continuous, modular society) - as in clonal organisms.

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.

food

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

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.

nocturnal

active during the night

nomadic

generally wanders from place to place, usually within a well-defined range.

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.

polymorphic

"many forms." A species is polymorphic if its individuals can be divided into two or more easily recognized groups, based on structure, color, or other similar characteristics. The term only applies when the distinct groups can be found in the same area; graded or clinal variation throughout the range of a species (e.g. a north-to-south decrease in size) is not polymorphism. Polymorphic characteristics may be inherited because the differences have a genetic basis, or they may be the result of environmental influences. We do not consider sexual differences (i.e. sexual dimorphism), seasonal changes (e.g. change in fur color), or age-related changes to be polymorphic. Polymorphism in a local population can be an adaptation to prevent density-dependent predation, where predators preferentially prey on the most common morph.

saltwater or marine

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

scavenger

an animal that mainly eats dead animals

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.

sperm-storing

mature spermatozoa are stored by females following copulation. Male sperm storage also occurs, as sperm are retained in the male epididymes (in mammals) for a period that can, in some cases, extend over several weeks or more, but here we use the term to refer only to sperm storage by females.

tactile

uses touch to communicate

temperate

that region of the Earth between 23.5 degrees North and 60 degrees North (between the Tropic of Cancer and the Arctic Circle) and between 23.5 degrees South and 60 degrees South (between the Tropic of Capricorn and the Antarctic Circle).

visual

uses sight to communicate

zooplankton

animal constituent of plankton; mainly small crustaceans and fish larvae. (Compare to phytoplankton.)

Ref­er­ences

Hatch, S., D. Net­tle­ship. 1998. North­ern ful­mar (Ful­marus glacialis). The Birds of North Amer­ica On­line, 361: 1-20. Ac­cessed July 13, 2009 at http://​bna.​birds.​cornell.​edu.​proxy.​lib.​umich.​edu/​bna/​species/​361.

Huettmann, F., A. Di­a­mond. 2000. Seabird mi­gra­tion in the Cana­dian north­west At­lantic Ocean: moult­ing lo­ca­tions and move­ment pat­terns of im­ma­ture birds. Cana­dian Jour­nal of Zo­ol­ogy, 78: 624-627.

del Hoyo, J., A. El­liott, J. Sar­gatal. 1992. Hand­book of the Birds of the World, Vol­ume I. Barcelona: Lynx Edi­cions.