Arctocephalus gazellaAntarctic fur seal

Ge­o­graphic Range

Arc­to­cephalus gazella, the Antarc­tic fur seal, has a very wide dis­tri­b­u­tion. They are mostly found in wa­ters south of the Antarc­tic Con­ver­gence, but some do in­habit areas slightly north of the Con­ver­gence. Most breed­ing pop­u­la­tions are found on South Geor­gia Is­land and Bird Is­land, while other pop­u­la­tions are found in the south Prince Ed­ward, Crozet, Ker­gue­len, and Mac­quarie Is­lands. Va­grants, how­ever, have been ob­served in the south­ern part of South Amer­ica and the Juan Fer­nan­dez Is­lands. Pop­u­la­tions in the south In­dian Ocean, south of the polar front, are found on Heard and Mc­Don­ald Is­lands and north of the polar front on dis­tances and have been seen from these breed­ing is­lands up to the ice edge of the polar front. Fe­males leave the breed­ing is­lands dur­ing the win­ter and be­tween breed­ing sea­sons trav­el­ling south to the mar­ginal ice zone and across the polar front. Bulls often re­main at the breed­ing is­lands dur­ing win­ter. Pups stay close to the beaches where they were born but usu­ally move on to the ocean as win­ter pro­gresses. (For­cada and Stani­land, 2009; Jef­fer­son, et al., 2008)

Habi­tat

Antarc­tic fur seals spend much of their time in the ocean, hunt­ing for food. While on land, they pre­fer to stay in rocky habi­tats but will go to beaches and zones of veg­e­ta­tion. Males can dive up to a max­i­mum of 350 me­ters, while fe­males can only reach up to 210 me­ters. Fe­males can travel long dis­tances in the open ocean for long pe­ri­ods of time be­tween breed­ing. (For­cada and Stani­land, 2009; Jef­fer­son, et al., 2008)

  • Range depth
    350 (high) m
    1148.29 (high) ft

Phys­i­cal De­scrip­tion

Sex­ual di­mor­phism is very ev­i­dent in Antarc­tic fur seals. Males are four to five times heav­ier than fe­males and one and a half times longer. The av­er­age length of the males is 180 cm while the av­er­age length of fe­males is 129 cm. The av­er­age weight of males is 133 kg and for fe­males it is just 34 kg. Their body is cov­ered in hair ex­cept for the areas around the rhi­nar­ium (area around the nos­trils), ear tips, and the pal­mar sur­face of the flip­pers. They have two dif­fer­ent lay­ers of hair, the un­der-pelt, which is made up of fine fur for in­su­la­tion, and the other layer, which has two dif­fer­ent types of guard hairs. These seals have nails on their hind flip­pers that are well de­vel­oped and used for groom­ing. Antarc­tic fur seals also have the longest fa­cial vib­ris­sae, or whiskers, of any other pin­niped, reach­ing up to 45 cm in bulls. The bod­ies in both males and fe­males are thick, with long necks. Males are gray­ish brown in color, while their face is a darker gray. The chest may ap­pear to be a sil­very gray color as well. They have a heavy, griz­zled mane. Fe­male coats are also gray­ish brown in color, but their chest and neck are often white to gray. Pups are born black, with a gray­ish brown belly. They later molt to be com­pletely gray­ish brown. About one out of every 100 pups born is born with leucis­tic morph re­sult­ing in a creamy white or yel­low white ex­posed skin, which is nor­mally pig­mented. They have large ca­nines that are used in ter­ri­to­r­ial fights among males. A strong cor­re­la­tion has been found be­tween can­ina length, mass, and width in male Antarc­tic fur seals and body size. (Acevedo, et al., 2008; For­cada and Stani­land, 2009; Hoff­man, et al., 2010)

  • Range mass
    34 to 133 kg
    74.89 to 292.95 lb
  • Range length
    129 to 180 cm
    50.79 to 70.87 in

Re­pro­duc­tion

Antarc­tic fur seals are polyg­y­nous and breed in colonies. Adult males ar­rive and es­tab­lish ter­ri­to­ries, about one month be­fore breed­ing fe­males come ashore, which is around mid Oc­to­ber or early No­vem­ber. Fe­males give birth to pups con­ceived from the pre­vi­ous sea­son. They mate again around six to seven days post-birth. Main­tain­ing ter­ri­to­ries is very costly for males. They lose about 1.5 kg in weight per day and ob­tain face in­juries from ter­ri­to­r­ial dis­putes. Con­se­quently, males do not tend to hold ter­ri­tory until they are at least eight years old. This also en­cour­ages a dom­i­nance hi­er­ar­chy on the breed­ing beaches. The most suc­cess­ful males de­fend the most de­sir­able ter­ri­to­ries (those near the water but above the high water mark). The weaker males oc­cupy ter­ri­to­ries higher up the beach. Each ter­ri­to­r­ial male is as­so­ci­ated with, on av­er­age, 15 fe­males or be­tween 1 to 27 fe­males. (Hoff­man and For­cada, 2011; Hoff­man, et al., 2003; Nowak and Walker, 2003)

Once re­turn­ing to shore fe­males give birth to one pup, on av­er­age, con­ceived from the pre­vi­ous year. The ges­ta­tion pe­riod is 11.75 months and im­plan­ta­tion is pos­si­bly de­layed. New­born pups weigh 6 kg on av­er­age. Males and fe­males re­turn to breed­ing sites, even within a few me­ters of pre­vi­ous ter­ri­to­ries. Sur­vival of their young from pre­vi­ous years prob­a­bly en­cour­ages re­turn­ing to the same spot year after year. Pups are born in Oc­to­ber or early No­vem­ber and weigh about six kilo­grams on av­er­age. While the mother is away, pups roam about and in­ter­act with each other. By early Jan­u­ary some pups are al­ready going to the water but can­not swim well until March. Fe­males use vo­cal­iza­tions to find the pup once she is back on land and con­firms the pup by scent. Pups are weaned at about 117 days and be­come re­pro­duc­tively ma­ture at three or four years old. (Hoff­man, et al., 2003; Nowak and Walker, 2003)

  • Breeding interval
    Antarctic fur seals breed once a year.
  • Breeding season
    Antarctic fur seals breed during the month of December.
  • Range number of offspring
    0 to 2
  • Average number of offspring
    1
    AnAge
  • Average gestation period
    11.75 months
  • Average gestation period
    257 days
    AnAge
  • Average weaning age
    117 days
  • Range age at sexual or reproductive maturity (female)
    3 to 4 years
  • Range age at sexual or reproductive maturity (male)
    3 to 4 years

Fe­male Antarc­tic fur seals have to reg­u­larly for­age for food dur­ing the growth of their pups. Fe­males al­ter­nate for­ag­ing trips with short suck­ling bouts until the pups are weaned after about 117 days. They for­age at sea for 1 to 13 days at a time with an av­er­age trip du­ra­tion of 5 days. They then re­turn to feed the pup for about two days be­fore re­turn­ing to sea. (Hoff­man and For­cada, 2011; Hoff­man, et al., 2003; Nowak and Walker, 2003)

  • Parental Investment
  • female parental care
  • pre-hatching/birth
    • protecting
      • female
  • pre-weaning/fledging
    • provisioning
      • female
    • protecting
      • female
  • pre-independence
    • provisioning
      • female
    • protecting
      • female

Lifes­pan/Longevity

In cap­tiv­ity the lifes­pan of Antarc­tic fur seals has not been well stud­ied and it re­mains un­known. In the wild, males live up to 15 years, while fe­males can live up to 25 years. (de Ma­g­a­l­haes and Costa, 2009)

Be­hav­ior

Antarc­tic fur seals are con­sid­ered to be one of the most ter­res­trial pin­nipeds along with the leop­ard seal. They are able to move across slip­pery rocks and through the dense grasses faster than hu­mans. On a smooth sur­face, they are able to reach up to 20 km per hour. They can ex­ceed this speed while swim­ming. After the breed­ing sea­son is over and pups are weaned, the seals move to sea dur­ing win­ter months of May through No­vem­ber. It is not known where they go and if it is a di­rec­tional mi­gra­tion or sim­ply dis­per­sal. Some adult males and ju­ve­nile seals stay ashore all year round. When for­ag­ing, dives usu­ally av­er­age about 30 m in depth and last about two min­utes. (Hoff­man, et al., 2003; Nowak and Walker, 2003)

  • Range territory size
    22 to 60 m^2

Home Range

Due to com­pe­ti­tion among males, ter­ri­tory size shrinks from 60 square me­ters in mid No­vem­ber to about 22 square me­ters in De­cem­ber. A dom­i­nance hi­er­ar­chy main­tains ter­ri­to­ries. (Hoff­man, et al., 2003; Nowak and Walker, 2003)

Com­mu­ni­ca­tion and Per­cep­tion

Antarc­tic fur seals use vo­cal­iza­tions to com­mu­ni­cate. Males use two main calls. One is a threat­en­ing roar which is di­rected to­wards other males. Else, it is used as a re­sponse to a spe­cific threat, such as a preda­tor. The other call they make is a "huff-chuff". This call is used when mov­ing around breed­ing ter­ri­to­ries, in­ter­act­ing with fe­males, and is used as a sign of sta­tus. Fe­males can roar and "huff-chuff", but their main form of com­mu­ni­ca­tion is with their pups. They use both sound and smell to es­tab­lish a bond. The sound is a high pitched call that is re­in­forced after the pup is born so when the mother re­turns from hunt­ing trips she can make the sound and the pup will rec­og­nize it. The mother and pup use smell at close dis­tances to con­firm each other's iden­tity. (For­cada and Stani­land, 2009)

Food Habits

Antarc­tic fur seals mainly feed on fish, krill, crus­tacean, and cephalopods, such as squid and oc­topods. Fish con­si­tute al­most 75% of the diet in non-win­ter months. At the South Geor­gia Is­lands, the main fish prey is the mack­erel ice­fish. How­ever, they also con­sume krill in large quan­ti­ties as well. Lac­tat­ing fe­males mainly feed on krill. If krill is un­avail­able, they turn to fish. Dur­ing win­ter months, adult and sub-adult males feed on 50% krill and 50% fish. They also prey on some smaller pen­guins (4-8 kg) as well, such as rock­hop­per and mac­a­roni pen­guins. Pre­vi­ous stud­ies sug­gested that fur seals only at­tacked king pen­guins on land, but Char­bon­nier et al. (2007) ob­served that adult males at­tack king pen­guins at sea, too. Al­though adult male and fe­male Antarc­tic fur seals chased king pen­guins at sea, only adult males were suc­cess­ful in catch­ing and killing or in­jur­ing the pen­guins. (Casaux, et al., 1998; Char­bon­nier, et al., 2007)

  • Primary Diet
  • carnivore
    • eats terrestrial vertebrates
    • piscivore
    • eats non-insect arthropods
  • Animal Foods
  • birds
  • fish
  • aquatic crustaceans

Pre­da­tion

One major preda­tor of Antarc­tic fur seeals are the leop­ard seals. They are a major con­trib­u­tor to high seal pup mor­tal­ity rates es­pe­cially be­tween Jan­u­ary and March be­fore the pups are weaned. This has lim­ited the growth of the colony at Ele­phant and Liv­ingston Is­lands in the South Shet­lands. Antarc­tic fur seals also are also preyed upon by killer whales and sharks. (Boveng, et al., 1998)

Ecosys­tem Roles

Mem­bers of Antarc­tic fur seals are key preda­tors of krill and var­i­ous species of fish and squid. It has been found that there is a cor­re­la­tion be­tween size of breed­ing colonies and prey avail­abil­ity, based upon short term en­vi­ron­men­tal changes and the ef­fect it has on the re­pro­duc­tive suc­cess of fe­males.

Lung­worms in­fect three mem­bers of the fur seals group. These par­a­sites in­fect the lungs of their host. ("Pro­posal to De-list Antarc­tic Fur Seals as Spe­cially Pro­tected Species", 2006; Dai­ley,, 2009)

Com­men­sal/Par­a­sitic Species
  • lung­worms Parafi­laroides species

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

In the 1800 and 1900s Antarc­tic fur seals were widely hunted for their fur. Since this time, how­ever, Antarc­tic fur seals have had lit­tle eco­nomic im­por­tance to hu­mans. Al­though, in­creas­ing com­mer­cial krill har­vest­ing could af­fect pop­u­la­tions in the fu­ture. ("Pro­posal to De-list Antarc­tic Fur Seals as Spe­cially Pro­tected Species", 2006; "Pro­posal to De-list Antarc­tic Fur Seals as Spe­cially Pro­tected Species", 2006)

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

There are no known ad­verse ef­fects of Antarc­tic fur seals on hu­mans.

Con­ser­va­tion Sta­tus

The num­ber of Antarc­tic fur seals were re­duced to below 3,000 in­di­vid­u­als in the 1800s. In 1964, they be­came a “spe­cially pro­tected species,” which is a term given only to the “most vul­ner­a­ble and en­dan­gered species,” (Pro­posal to De-list, 2006). Since then, Antarc­tic fur seals have greatly ex­tended their range and are at lit­tle risk of ex­tinc­tion. Total pop­u­la­tion num­bers are es­ti­mated at four to seven mil­lion seals and are in­creas­ing. In the CITES ap­pen­dices Antarc­tic fur seals are listed in Ap­pen­dix II, in­di­cat­ing that while they are not cur­rently threat­ened with ex­tinc­tion they may be­come so un­less trade is closely con­trolled. ("Pro­posal to De-list Antarc­tic Fur Seals as Spe­cially Pro­tected Species", 2006)

Con­trib­u­tors

Car­son Widener (au­thor), Rad­ford Uni­ver­sity, Karen Pow­ers (ed­i­tor), Rad­ford Uni­ver­sity, Kier­sten Newtoff (ed­i­tor), Rad­ford Uni­ver­sity, Melissa Whistle­man (ed­i­tor), Rad­ford Uni­ver­sity, Laura Podzikowski (ed­i­tor), Spe­cial Pro­jects.

Glossary

Antarctica

lives on Antarctica, the southernmost continent which sits astride the southern pole.

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.

delayed implantation

in mammals, a condition in which a fertilized egg reaches the uterus but delays its implantation in the uterine lining, sometimes for several months.

dominance hierarchies

ranking system or pecking order among members of a long-term social group, where dominance status affects access to resources or mates

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.

female parental care

parental care is carried out by females

motile

having the capacity to move from one place to another.

native range

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

pelagic

An aquatic biome consisting of the open ocean, far from land, does not include sea bottom (benthic zone).

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.

polygynous

having more than one female as a mate at one time

saltwater or marine

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

sexual

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

sexual ornamentation

one of the sexes (usually males) has special physical structures used in courting the other sex or fighting the same sex. For example: antlers, elongated tails, special spurs.

tactile

uses touch to communicate

terrestrial

Living on the ground.

territorial

defends an area within the home range, occupied by a single animals or group of animals of the same species and held through overt defense, display, or advertisement

visual

uses sight to communicate

Ref­er­ences

Antarc­tic Treaty Con­sul­ta­tive Meet­ing. Pro­posal to De-list Antarc­tic Fur Seals as Spe­cially Pro­tected Species. WP039. Ed­in­burgh: Sec­re­tariat of the Antarc­tic Treaty. 2006. Ac­cessed April 24, 2012 at http://​www.​scar.​org/​treaty/​atcmxxix/​atcm29_​wp039.​pdf.

Acevedo, J., D. Tor­res, A. Aguayo-Lobo. 2008. Rare piebald and par­tially leucis­tic Antarc­tic fur seals, Arc­to­cephalus gazella, at Cape Shirreff, Liv­ingston Is­land, Antarc­tica. Polar Bi­ol­ogy, 32/1: 41-45.

Boveng, P., L. Hiruki, M. Schwartz, J. Bengston. 1998. Pop­u­la­tion growth of the Antarc­tic fur seals: Lim­i­ta­tion by a top preda­tor, the leop­ard seal?. Ecol­ogy So­ci­ety of Amer­ica, 79/8: 2863-2877.

Boyd, I., A. Mur­ray. 2001. Mon­i­tor­ing a ma­rine ecosys­tem using re­sponses of upper trophic level preda­tors. Jour­nal of An­i­mal Ecol­ogy, 70/5: 747-760.

Casaux, R., A. Ba­roni, A. Car­lini. 1998. The diet of the Antarc­tic fur seal Arc­to­cephalus gazella at Har­mony Point, Nel­son Is­land, South Shet­land Is­lands. Polar Bi­ol­ogy, 20/6: 424-428.

Char­bon­nier, Y., K. De­lord, J. Thei­bot. 2007. King-size fast food for Antarc­tic fur seals. Polar Bi­ol­ogy, 33/5: 721-724.

Dai­ley,, M. 2009. A new species of Parafi­laroides (Ne­ma­toda: Fi­laroi­di­dae) in three species of fur seals (Car­nivora: Otari­idae) from the South­ern Hemi­sphere. Amer­i­can So­ci­ety of Par­a­sitol­o­gists, 95/1: 156-159.

For­cada, J., I. Stani­land. 2009. Antarc­tic Fur Seal Arc­to­cephalus gazella. Pp. 36-42 in W Per­rin, B Wur­sig, J Thewis­sen, eds. En­cy­clo­pe­dia of Ma­rine Mam­mals, Vol. 2, 2nd Edi­tion. New York: El­se­vier.

Gaste­bois, C., M. Vi­viant, C. Guinet. 2011. On­togeny of aquatic be­hav­iours in Antarc­tic fur seal (Arc­to­cephalus gazella) pups in re­la­tion to growth per­for­mances at Ker­gue­len Is­lands. Polar Bi­ol­ogy, 34/7: 1097-1103.

Hoff­man, J., I. Boyd, W. Amos. 2003. Male re­pro­duc­tive strat­egy and the im­por­tance of ma­ter­nal sta­tus in the Antarc­tic fur seal Arc­to­cephalus gazella. Evo­lu­tion, 57/8: 1917-1930.

Hoff­man, J., J. For­cada. 2011. Ex­treme natal philopa­try in fe­male Antarc­tic fur seals (Arc­to­cephalus gazella). Mam­malian Bi­ol­ogy, 77/1: 71-73.

Hoff­man, J., N. Han­son, J. For­cada, P. Trathan, W. Amos. 2010. Get­ting long in the tooth: A strong pos­i­tive cor­re­la­tion be­tween ca­nine size and het­erozy­gos­ity in Antarc­tic fur seals Arc­to­cephalus gazella. Jour­nal of Hered­ity, 101/5: 527-538.

Jabour, J. 2008. Suc­cess­ful con­ser­va­tion- then what? The de-list­ing of Arc­to­cephalus fur seal species in Antarc­tica. Jour­nal of In­ter­na­tional Wildlife and Pol­icy, 11/1: 1-29.

Jef­fer­son, T., M. Web­ber, R. Pit­man. 2008. Ma­rine Mam­mals of the World. New York: El­se­vier.

Lea, M., M. Hin­dell, C. Guinet, S. Goldswor­thy. 2001. Vari­abil­ity in the div­ing ac­tiv­ity of Antarc­tic fur seals, Arct­cephalus gazella, at Iles Ker­gue­len. Polar Bi­ol­ogy, 25/4: 269-279.

Luque, S., J. Arnould, E. Miller, Y. Cherel, C. Guinet. 2007. For­ag­ing be­hav­iour of sym­patric Antarc­tic and sub­antarc­tic fur seals: Does their con­trast­ing du­ra­tion of lac­ta­tion make a dif­fer­ence?. Ma­rine Bi­ol­ogy, 152/1: 213-224.

Makhado, A., M. Bester, S. Kirk­man, P. Pis­to­rius, J. Fer­gu­son, N. Klages. 2007. Prey of the Antarc­tic fur seal Arc­to­cephalus gazella at Mar­ion Is­land. Polar Bi­ol­ogy, 31/5: 575-581.

Nowak, R., E. Walker. 2003. Arc­to­cephalus gazella. Pp. 77-78 in Walker's Ma­rine Mam­mals of the World, Vol. 6, Sixth Edi­tion. Bal­ti­more: The Johns Hop­kins Uni­ver­sity Press.

Osman, L., R. Hucke- Gaete, C. Moreno, D. Tor­res. 2003. Feed­ing ecol­ogy of Antarc­tic fur seals at Cape Shirreff, South Shet­lands, Antarc­tica. Polar Bi­ol­ogy, 27/2: 92-98.

Reid, K., J. Crox­all. 2001. En­vi­ron­men­tal re­sponse of up­per-trophic level preda­tors re­veals a sys­tem change in an Antarc­tic ma­rine ecosys­tem. Pro­ceed­ings: Bi­o­log­i­cal Sci­ences, 268/1465: 377-384.

Stani­land, I., I. Boyd, K. Reid. 2007. An en­ergy–dis­tance trade-off in a cen­tral-place for­ager, the Antarc­tic fur seal (Arc­to­cephalus gazella). Ma­rine Bi­ol­ogy, 152/2: 233-241.

Tor­res, D., J. Acevedo, D. Tor­res, R. Var­gas, A. Aguayo-Lobo. 2011. Va­grant Sub­antarc­tic fur seal at Cape Shirreff, Liv­ingston Is­land, Antarc­tica. Polar Bi­ol­ogy, 35/3: 469-473.

de Ma­g­a­l­haes, J., J. Costa. 2009. A data­base of ver­te­brate longevity records and their re­la­tion to other life his­tory traits. Jour­nal of Evo­lu­tion­ary Bi­ol­ogy, 22/8: 1770-1774.