Hydrurga leptonyxleopard seal

Ge­o­graphic Range

Leop­ard seals (Hy­drurga lep­tonyx) are pre­dom­i­nately found in the cir­cum­po­lar re­gion of the Antarc­tic pack ice. Al­though small num­bers can be found just be­yond the pack ice on the nearby sub­antarc­tic is­lands year-round, there is greater dis­per­sal into this area dur­ing the win­ter months. (Orit­s­land, 1970; Rogers, 2009)

Habi­tat

Leop­ard seals re­side mostly on and around the pack ice of Antarc­tica, but may also be seen on the sub­antarc­tic is­lands if there is enough ice sub­strate. These seals are much more agile in the water than on ice, and water is where they spend much of their time. Leop­ard seals feed on species that re­side in the sur­face wa­ters of the ocean, and thus are found pri­mar­ily in these wa­ters. (Jes­sopp, et al., 2004; Laws, 1984; Orit­s­land, 1970)

  • Terrestrial Biomes
  • icecap

Phys­i­cal De­scrip­tion

Leop­ard seals are by far the largest of the antarc­tic seals. Males can grow up to 3 me­ters in length and weigh ap­prox­i­mately 300 kg. Fe­males are even larger, grow­ing up to 3.8 me­ters in length and 500 kg. The over­all body shape of leop­ard seals are long and slen­der, mak­ing it very agile in the water. Their col­or­ing varies dor­sally to ven­trally with a dark grey back, a sil­very grey un­der­side, and dark and light spots through­out the en­tire body. The snout of leop­ard seals are long on their large head; well-de­signed for catch­ing and han­dling prey. (Ray, 1970; Rogers, 2009)

  • Sexual Dimorphism
  • female larger
  • Range mass
    300 to 500 kg
    660.79 to 1101.32 lb
  • Range length
    3 to 3.8 m
    9.84 to 12.47 ft

Re­pro­duc­tion

Lit­tle is known about leop­ard seal mat­ing sys­tems, be­cause they in­habit an ex­treme en­vi­ron­ment mak­ing di­rect ob­ser­va­tion dif­fi­cult. Much of what is known was ob­served from cap­tive in­di­vid­u­als. Lit­tle is known about mate ac­qui­si­tion in leop­ard seals, but vo­cal­iza­tion is thought to play a role as males be­come highly vocal dur­ing the breed­ing sea­son. Mat­ing oc­curs in the water in cap­tive en­vi­ron­ments and wild pop­u­la­tions are thought to be­have sim­i­larly. After mat­ing the fe­male is left alone to wean the pups on the ice. (Rogers, 2009)

Birth of leop­ard seal pups gen­er­ally oc­curs be­tween late Oc­to­ber and No­vem­ber, with new­born pups mea­sur­ing on av­er­age 120 cm in length. For the next 4 weeks, the mother nurses her pups on an ice flow. Mat­ing oc­curs dur­ing De­cem­ber and into the be­gin­ning of Jan­u­ary shortly after the pups are weaned. (Jef­fer­son, et al., 1993; Orit­s­land, 1970; Rogers, 2009; Siniff, 1991)

  • Breeding interval
    Leopard seals breed once yearly.
  • Breeding season
    The breeding lasts from December to early January.
  • Range number of offspring
    1 (high)
  • Average number of offspring
    1
  • Average number of offspring
    1
    AnAge
  • Average gestation period
    274 days
    AnAge
  • Range weaning age
    4 (high) weeks
  • Average age at sexual or reproductive maturity (female)
    4 years
  • Average age at sexual or reproductive maturity (female)
    Sex: female
    1095 days
    AnAge
  • Average age at sexual or reproductive maturity (male)
    4.5 years
  • Average age at sexual or reproductive maturity (male)
    Sex: male
    1461 days
    AnAge

Leop­ard seals live a soli­tary life with the ex­cep­tion of a brief mat­ing pe­riod, so there is lit­tle in­for­ma­tion de­scrib­ing mat­ing in­ter­ac­tions of males and fe­males. It is, how­ever, known that males do not pro­vide any post-fer­til­iza­tion parental in­vest­ment once they have mated with a fe­male. (Rogers, 2009)

Fe­male leop­ard seals are solely re­spon­si­ble for their pup once it is born. On the ice floes of Antarc­tica mother seals are seen nurs­ing and pro­tect­ing their young for ap­prox­i­mately 4 weeks fol­low­ing birth. After these 4 weeks, the pup is weaned and shortly after fe­males begin mat­ing again. After the wean­ing pe­riod, there is not much known about leop­ard seal de­vel­op­ment. Ju­ve­nile leop­ard seals have, how­ever, been ob­served in rel­a­tively large num­bers on the nearby sub­antarc­tic is­lands. (Rogers, 2009; Siniff, 1991)

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

Lifes­pan/Longevity

There are few ac­counts of the lifes­pan of leop­ard seals. How­ever, they have been recorded to live for up to 30 years in the wild, but the lifes­pan is spec­u­lated to be closer to 26 years. (Orit­s­land, 1970; Rogers, 2009)

Be­hav­ior

Leop­ard seals are a soli­tary species ex­clud­ing mat­ing and nurs­ing pe­ri­ods. As mat­ing sea­son ap­proaches, the den­sity of seals on and around packs of ice in­creases. Den­sity on pack ice also in­creases when pups are born, as that is where moth­ers give birth and nurse their young. Oth­er­wise leop­ard seals pre­dom­i­nately in­habit the water. (Laws, 1984; Rogers, 2009; Siniff, 1991)

Home Range

The home range of leop­ard seals is con­fined mostly to the pack ice, be­cause of mat­ing. Through­out the year are also found on the nearby sub­antarc­tic is­lands in mod­er­ately low num­bers. How­ever, this greatly in­creases dur­ing the win­ter months dur­ing the seal mi­gra­tion pe­riod. (Jes­sopp, et al., 2004; Orit­s­land, 1970; Rogers, 2009)

Com­mu­ni­ca­tion and Per­cep­tion

Not much is known re­gard­ing com­mu­ni­ca­tion among leop­ard seals. How­ever, males are known to vo­cal­ize just prior to and dur­ing the mat­ing sea­son. It is sus­pected that these sounds are used for mate at­trac­tion. (Opzee­land, et al., 2010)

Food Habits

Leop­ard seals feed pri­mar­ily on krill, using their lo­bodont teeth to fil­ter these small crus­taceans from the water. Al­though krill are their pri­mary food source, leop­ard seals are also ag­gres­sive apex preda­tors eat­ing pen­guins, young crabeater seals, and squid. (Berk­man, 2001; Rogers, 2009)

  • Animal Foods
  • birds
  • mammals
  • fish
  • mollusks
  • aquatic crustaceans

Pre­da­tion

Leop­ard seals are apex preda­tors, in­di­cat­ing that they are at the top of the Antarc­tic food chain. Their only known nat­ural preda­tors are killer whales, how­ever leop­ard seals are rarely eaten. (Berk­man, 2001)

Ecosys­tem Roles

As apex preda­tors, leop­ard seals play an im­por­tant eco­log­i­cal role feed­ing on large an­i­mals that in­habit the ex­treme antarc­tic sys­tem. (Rogers, 2009)

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

There are few in­ter­ac­tions be­tween hu­mans and leop­ard seals, how­ever they are used for sci­en­tific re­search and ed­u­ca­tion. (Jef­fer­son, et al., 1993)

  • Positive Impacts
  • research and education

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

Leop­ard seals have no ob­served neg­a­tive eco­nomic ef­fects on hu­mans. (Jef­fer­son, et al., 1993)

Con­ser­va­tion Sta­tus

Ac­cord­ing to the IUCN Red List, leop­ard seals are at lower risk and of least con­cern. How­ever, a de­cline in antarc­tic pack ice will likely to be im­pact the species. ("2008 Pa­cific is­lands red list for an­i­mals", 2008)

Other Com­ments

The sci­en­tific name of leop­ard seals, Hy­drurga lep­tonyx, lit­er­ally trans­lated means 'slen­der-clawed wa­ter-worker'. (Rogers, 2009)

Con­trib­u­tors

Anna Hill (au­thor), Michi­gan State Uni­ver­sity, Bar­bara Lun­dri­gan (ed­i­tor), Michi­gan State Uni­ver­sity, Laura Podzikowski (ed­i­tor), Spe­cial Pro­jects.

Glossary

Antarctica

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

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

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

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.

female parental care

parental care is carried out by females

filter-feeding

a method of feeding where small food particles are filtered from the surrounding water by various mechanisms. Used mainly by aquatic invertebrates, especially plankton, but also by baleen whales.

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

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.

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.

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

solitary

lives alone

tactile

uses touch to communicate

viviparous

reproduction in which fertilization and development take place within the female body and the developing embryo derives nourishment from the female.

Ref­er­ences

2008. "2008 Pa­cific is­lands red list for an­i­mals" (On-line). IUCN.​org. Ac­cessed March 11, 2012 at http://​cmsdata.​iucn.​org/​downloads/​appendix_​1_​animals_​of_​the_​pacific_​islands_​listed_​on_​the_​2008_​red_​list.​pdf.

Berk­man, P. 2001. Sci­ence into Pol­icy : Global Lessons from Antarc­tica. Burling­ton, MA: Aca­d­e­mic Press.

Jef­fer­son, T., S. Leather­wood, M. Web­ber. 1993. Ma­rine Mam­mals of the World. Roome: United Na­tions En­vi­ron­ment Pro­gramme, Food and Agri­cul­ture Or­ga­ni­za­tion of the United Na­tions.

Jes­sopp, M., J. Reid, P. Trathan, E. Mur­phy. 2004. Win­ter dis­per­sal of leop­ard seals (Hy­drurga lep­tonyx): en­vi­ron­men­tal fac­tors in­flu­enc­ing de­mo­graph­ics and sea­sonal abun­dance. Jour­nal of Zo­ol­ogy, 263: 251-258.

Laws, R. 1984. Antarc­tic Ecol­ogy Vol. II. Lon­don: Aca­d­e­mic Press.

Opzee­land, I., S. Par­ijs, H. Borne­mann, S. Frick­en­haus, L. Kin­der­mann, H. Klinck, J. Plotz, O. Boebel. 2010. Acoustic ecol­ogy of Antarc­tic pin­nipeds. Ma­rine Ecol­ogy Progress Se­ries, 414: 267-291.

Orit­s­land, T. 1970. Bi­ol­ogy and Pop­u­la­tion Dy­nam­ics of Antarc­tic Seals. Pp. 361-366 in M Holdgate, ed. Antarc­tic Ecol­ogy, Vol. I. Lon­don: Aca­d­e­mic Press.

Ray, C. 1970. Pop­u­la­tion Ecol­ogy of Antarc­tic Seals. Pp. 398-414 in M Holdgate, ed. Antarc­tic Ecol­ogy, Vol. 1. Lon­don, New York: Aca­d­e­mic Press.

Rogers, T. 2009. "Leop­ard seal (H. lep­tonyx)" (On-line). The So­ci­ety for Ma­rine Mam­mal­ogy. Ac­cessed March 11, 2012 at http://​www.​marinemammalscience.​org/​index.​php?​option=com_​content&​view=article&​id=459&​Itemid=298.

Siniff, D. 1991. An Overview of the Ecol­ogy of Antarc­tic Seals. Amer­i­can Zo­ol­o­gist, 31: 143-149.