Grampus griseusRisso's dolphin

Ge­o­graphic Range

Gram­pus griseus has an ex­ten­sive dis­tri­b­u­tion. The species can be found in tem­per­ate, sub­trop­i­cal and trop­i­cal wa­ters of oceans world­wide. ("NOAA fish­eries", 2010; Amano and Miyazaki, 2004; Nuno, 2008; Pawloski, et al., 2003; Stew­art, et al., 2002)

Habi­tat

Risso's dol­phins are pelagic, but pre­fer habi­tat on steep slopes, rang­ing from 400 to 1,200 me­ters. They are often seen near the edges of con­ti­nen­tal shelves, or near ba­thy­met­ric fea­tures such as seamounts and sub­ma­rine canyons. They are most com­monly found in wa­ters rang­ing in tem­per­a­ture from 59 to 68 de­grees F, but will in­habit wa­ters cold as 50 de­grees F. ("NOAA fish­eries", 2010; Leather­wood, et al., 1980; Nuno, 2008; Pawloski, et al., 2003; Tay­lor, et al., 2010)

Risso’s dol­phins are pre­sent year round through­out most of their ge­o­graphic range. Res­i­dents of the north­ern-most parts of their range mi­grate sea­son­ally be­tween sum­mer­ing and win­ter­ing grounds For ex­am­ple, pop­u­la­tions off the coast of north­ern Scot­land dur­ing the sum­mer, mi­grate to the Mediter­ranean dur­ing the win­ter, and pop­u­la­tions off the coast of Cal­i­for­nia dur­ing the sum­mer, mi­grate to Mex­i­can wa­ters dur­ing win­ter. (Culik, 2010)

  • Range depth
    400 to 1,200 m
    1312.34 to ft

Phys­i­cal De­scrip­tion

Risso's dol­phins have blunt, squar­ish heads and lack the beak typ­i­cal of other del­phinids. The dor­sal fin is tall and fal­cate, and their flip­pers are long, pointed, and re­curved. The an­te­rior part of the body is very ro­bust, ta­per­ing to a nar­row tail­stock. Adults range from 2.6 to 4 m in length, with an av­er­age body mass around 400 kg. The sexes are sim­i­lar in size. New­borns range from 1.1 to 1.5 m in length and av­er­age 20 kg at birth. Along the body axis on the melon (i.e., beak, eyes, blow­hole) there is a slight con­cave groove which is a unique char­ac­ter­is­tic of this species. Sex­ual di­mor­phism has not been re­ported in this species. ("NOAA fish­eries", 2010; Jef­fer­son, et al., 1993; Pawloski, et al., 2003; Stew­art, et al., 2002)

The youngest calves range in colour from iri­des­cent gun­metal grey to fawn-brown dor­sally and are creamy-white ven­trally. Pale ochre-yel­low high­lights ac­cen­tu­ate the muz­zle. A white an­chor-shape patch be­tween the flip­pers re­sem­bles the chest chevron seen on pilot whales but is typ­i­cally brighter and more ex­ten­sive. Calves be­come sil­ver-grey, then darken to nearly black, re­tain­ing the ven­tral patches of white. As an­i­mals age fur­ther, their heads, ab­domens, and flanks lighten. (Nishi­waki 1972, Kruse et al. 1999, MMSC 1996, ("NOAA fish­eries", 2010; Jef­fer­son, et al., 1993; Stew­art, et al., 2002)

This species dis­plays highly vari­able col­oration. The youngest calves range in colour from iri­des­cent gun­metal grey to fawn-brown dor­sally and are creamy-white ven­trally. Pale ochre-yel­low high­lights ac­cen­tu­ate the muz­zle. A white an­chor-shape patch be­tween the flip­pers re­sem­bles the chest chevron seen on pilot whales but is typ­i­cally brighter and more ex­ten­sive. Calves be­come sil­ver-grey, then darken to nearly black, re­tain­ing the ven­tral patches of white. In older an­i­mals, lip colour fre­quently con­trasts with the sur­round­ing back­ground. Col­oration fades with age, and some adults ap­pear al­most com­pletely white due to the lin­ear scar­ring that ac­cu­mu­lates on in­di­vid­u­als over time. These dis­tinc­tive scars ac­cu­mu­late pri­mar­ily on the an­i­mals' dor­sal and lat­eral sur­faces and have been hy­poth­e­sized to re­sult from the com­bined ef­fects of lack of repig­men­ta­tion of dam­aged tis­sue and a slower heal­ing process than that ob­served in an­i­mals such as bot­tlenose dol­phins. Scar­i­fi­ca­tion can be caused by other Risso's dol­phins, preda­tors (e.g., cookie cut­ter sharks), prey, or by par­a­sites like sea lam­prey. In­traspe­cific, tooth rake, scars tend to be long and par­al­lel and may act as an in­di­ca­tor of male fit­ness dur­ing ag­gres­sive so­cial in­ter­ac­tions. ("NOAA fish­eries", 2010; Hart­man, et al., 2008; Jef­fer­son, et al., 1993; MacLeod, 1998)

Risso's dol­phins lack teeth in their upper jaws, but have 2 to 7 pairs of sharp peg-like teeth in their lower jaw, which are spe­cial­ized for cap­tur­ing prey, fight­ing preda­tors, and com­pet­ing with con­spe­cific for mates and re­sources. Evo­lu­tion­ary re­ten­tion of these teeth may be partly due to their sig­nif­i­cance in male-male in­ter­ac­tions. ("NOAA fish­eries", 2010; Jef­fer­son, et al., 1993; MacLeod, 1998; Stew­art, et al., 2002)

Risso's dol­phins may be con­fused with bot­tlenose dol­phins, false killer whales, and killer whales due to the shape and size of their dor­sal fin. How­ever, their blunt heads and ex­ten­sive scar­ring make them un­mis­tak­able. ("NOAA fish­eries", 2010)

  • Sexual Dimorphism
  • sexes alike
  • Range mass
    300 to 500 kg
    660.79 to 1101.32 lb
  • Range length
    2.6 to 5 m
    8.53 to 16.40 ft
  • Average length
    2.8 m
    9.19 ft

Re­pro­duc­tion

There is no in­for­ma­tion re­gard the mat­ing sys­tem of Gram­pus griseus. How­ever, other Cetaceans tend to be ei­ther polyg­y­nous and polyan­drous. (Stew­art, et al., 2002)

There is lit­tle in­for­ma­tion avail­able re­gard­ing re­pro­duc­tive be­hav­ior in Gram­pus griseus. Most fe­males are sex­u­ally ma­ture by 8 to 10 years old, how­ever, size is often a bet­ter in­di­ca­tor of sex­ual ma­tu­rity than age in ma­rine cetaceans. Most males reach sex­u­ally ma­tu­rity at a length of 2.6 to 2.8 m. Ges­ta­tion lasts 13 to 14 months, and av­er­age mass of new­borns calves is 20 kg. Wean­ing is com­plete by 12 to 18 months after par­tu­ri­tion. Breed­ing and calv­ing occur year-round, but peak dur­ing sum­mer and win­ter in the north At­lantic and east­ern Pa­cific, re­spec­tively. ("NOAA fish­eries", 2010; Nuno, 2008)

  • Breeding season
    Grampus griseus breeds year round, but peaks seasonally depending on hemisphere.
  • Average number of offspring
    1
    AnAge
  • Range gestation period
    13 to 14 months
  • Range weaning age
    12 to 18 months
  • Range age at sexual or reproductive maturity (female)
    8 to 10 years

Fe­male Risso's dol­phins are the pri­mary care givers to calves, and pa­ter­nal care, which is rare in other cetaceans, has not been doc­u­mented in this species. New­borns are pre­co­cial and begin swim­ming im­me­di­ately after birth. Mother-calf pods form, and young usu­ally do not leave the group until a few years be­fore sex­ual ma­tu­rity. Al­lo­parental care has been recorded amongst fe­males. Often, while a calve's mother is for­ag­ing for food, an­other fe­male pro­vides care. (Hart­man, et al., 2008)

  • Parental Investment
  • precocial
  • female parental care
  • pre-hatching/birth
    • provisioning
      • female
    • protecting
      • female
  • pre-weaning/fledging
    • provisioning
      • female
    • protecting
      • female
  • post-independence association with parents

Lifes­pan/Longevity

On av­er­age Risso's dol­phins live at least 30 years. ("NOAA fish­eries", 2010)

Be­hav­ior

Un­like most cetaceans, which tend to have ei­ther a fu­sion-fis­sion or ma­tri­lin­eally based so­cial sys­tem, Risso's dol­phins dis­play a strat­i­fied so­cial sys­tem. Clus­ters are formed based on age and sex class, with strongest as­so­ci­a­tions oc­cur­ring be­tween adult fe­males and adult males. Fe­male re­pro­duc­tive suc­cess is pos­i­tively in­flu­enced by the in­creased so­cial sup­port and for­ag­ing ben­e­fits of larger pods. For ex­am­ple, while a given fe­male is search­ing for food, she is able leave her calf in the care of other fe­males in the group. As a re­sult, fe­male pods tend to be much larger than those of males. Male for­ma­tions ex­pe­ri­ence a trade off in re­la­tion to size, as for­ag­ing ben­e­fits and habi­tat de­fense in­crease with pod size, but re­pro­duc­tive ben­e­fits de­crease due to in­creased com­pe­ti­tion for mates. Risso's dol­phins are very so­cial, and as many as 4,000 in­di­vid­u­als have been doc­u­mented in a sin­gle pod. Al­though es­ti­mates for the av­er­age pod size have var­ied over the years, re­cent stud­ies sug­gest a mean pod size of 3 to 12 in­di­vid­u­als. (Hart­man, et al., 2008; Kruse, et al., 1999; Nuno, 2008; Stew­art, et al., 2002)

Risso’s dol­phins spend 77% of their time trav­el­ing, 13% en­gaged in so­cial ac­tiv­ity, 5% feed­ing, and about 3.7% rest­ing. They feed at night, as that is when their pri­mary prey, cephalopods, travel to the ocean sur­face. Risso's dol­phins use a va­ri­ety of be­hav­iors to com­mu­ni­cate with con­specifics, such as chas­ing, bit­ing, aer­ial ac­ro­bat­ics, lob-tail­ing, and breach­ing. Males are often found ha­rass­ing other species, such as false killer whales and bot­tlenose dol­phins. Ag­gres­sive phys­i­cal con­tact has been doc­u­mented, such as flip­per slap­ping be­tween in­di­vid­u­als, stik­ing with flukes and dor­sal fins, and body blows (Kruse 1999, MMSC 1996). ("NOAA fish­eries", 2010; Hart­man, et al., 2008; Kruse, et al., 1999; Nuno, 2008; Stew­art, et al., 2002)

Risso’s dol­phins have been recorded as­so­ci­at­ing and form­ing groups with other cetaceans, in­clud­ing bot­tlenose dol­phins and Pa­cific white-sided dol­phins. Hy­brid off­spring be­tween bot­tlenose dol­phins and Risso’s dol­phins have been known to occur, both in cap­tiv­ity and in the wild. ("NOAA fish­eries", 2010; Kruse, et al., 1999)

Home Range

There is no in­for­ma­tion re­gard­ing home-range size in Risso’s dol­phins.

Com­mu­ni­ca­tion and Per­cep­tion

Risso’s dol­phins use echolo­ca­tion to lo­cate, iden­tify, and de­ter­mine the dis­tance of var­i­ous ob­jects in their en­vi­ron­ment. One of the most well-known sounds of del­phinids are clicks. The clicks of Risso's dol­phins have a peak fre­quency of 65 kHz, 3-dB band­widths of 72 kHz, and du­ra­tions of 40 to 100 Ms, all of which are con­sis­tent with other del­phinids. Risso’s dol­phins are also able to emit sonar clicks in the water while the ma­jor­ity of their fore­head is above water, a char­ac­ter­is­tic unique to this species. In ad­di­tion to broad­band clicks, Risso's dol­phins make a num­ber of dif­fer­ent vo­cal­iza­tions, in­clud­ing barks, buzzes, grunts, chirps, whis­tles, and si­mul­ta­ne­ous whis­tle and pulse sounds. Whis­tle and burst-pulse vo­cal­iza­tions have not been re­ported in other cetaceans and are thought to be unique to this species. (Corkeron and Van Par­ijs, 2001; Pawloski, et al., 2003)

Food Habits

Risso's dol­phins are known to prey on a mix of ner­itic, oceanic, and oc­ca­sion­ally bot­tom dwelling or­gan­isms. Their diet con­sists of fish, krill, crus­taceans, and cephalopods. Their most im­por­tant prey item is the greater arg­onaut, which is also known as the paper nau­tilus. They often fol­low prey into shal­low wa­ters along the con­ti­nen­tal shelf, and pre­fer to feed be­tween 600 and 800 m below the sur­face of the sea. ("NOAA fish­eries", 2010; Jef­fer­son, et al., 1993; Kruse, et al., 1999; Raga, et al., 2006; Stew­art, et al., 2002)

  • Animal Foods
  • fish
  • mollusks
  • aquatic crustaceans

Pre­da­tion

There is no in­for­ma­tion avail­able re­gard­ing preda­tors spe­cific to Risso's dol­phin. (Stew­art, et al., 2002)

Ecosys­tem Roles

Risso's dol­phins con­sume large amounts of fish, krill, crus­taceans, and cephalopods and likely have a sig­nif­i­cant in­flu­ence on the abun­dance of these an­i­mals. Risso's dol­phins are one of many hosts for sea lam­prey, which is com­mon in shore­line habi­tat through­out north At­lantic. ("NOAA fish­eries", 2010; Stew­art, et al., 2002)

Com­men­sal/Par­a­sitic Species

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

In In­done­sia and the Caribbean, Risso’s dol­phins are hunted for their meat and oil. In Japan, they are taken pe­ri­od­i­cally for food and fer­til­izer. Small num­bers are some­times col­lected for live ex­hi­bi­tions. ("NOAA fish­eries", 2010; Kruse, et al., 1999)

  • Positive Impacts
  • food
  • body parts are source of valuable material

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

Risso’s dol­phins are some­times a by-catch in the U.S. tuna purse seine in­dus­try, and are taken oc­ca­sion­ally in coastal gill net and squid sein­ing in­dus­tries off the U.S. coast. They are some­times a con­sid­ered a nui­sance to fish­er­man. Risso’s dol­phins are high trophic level con­sumers. As a re­sult, their tis­sues ac­cu­mu­late pol­lu­tants that are preva­lent through­out their ge­o­graphic range, a process known as bioac­cu­mu­la­tion, and con­sum­ing the meat of this species could be harm­ful. (Stew­art, et al., 2002; Storelli and Macrot­ri­giano, 2000)

Con­ser­va­tion Sta­tus

Risso's dol­phins are abun­dant and have a broad ge­o­graphic range. As a re­sult, they are clas­si­fied as a species of "least con­cern" on the IUCN's Red List of Threat­ened Species. How­ever, be­cause lit­tle is known of cur­rent pop­u­la­tion trends, it is dif­fi­cult to es­ti­mate po­ten­tial con­ser­va­tion needs. Po­ten­tial threats in­clude di­rect killings for meat and oil in the In­dian Ocean, and by-catch in the north At­lantic, the Mediter­ranean Sea, the south­ern Caribbean, the Azores, Peru, and the Solomon Is­lands. Be­cause this species re­lies on echolo­ca­tion to hunt, it is also thought that an­thro­pogenic sounds may in­flu­ence local pop­u­la­tions. Re­cent cli­mate change may also in­flu­ence their range and abun­dance, how­ever, po­ten­tial ef­fects are cur­rently un­clear. (Stew­art, et al., 2002)

Other Com­ments

The word "gram­pus" is Latin for "a kind of whale" and the word "griseus" is Latin for "gray". Pelorus Jack, a fa­mous Risso's dol­phin, had the habit of play­ing about ships and seemed to guide them into Pelorus Sound. It was ob­served for 24 years (around the turn of the cen­tury) es­cort­ing ships. (Kruse, et al., 1999)

Con­trib­u­tors

Kelsey Hans (au­thor), Uni­ver­sity of Michi­gan-Ann Arbor, Phil Myers (ed­i­tor), Uni­ver­sity of Michi­gan-Ann Arbor, John Berini (ed­i­tor), An­i­mal Di­ver­sity Web Staff.

Glossary

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

benthic

Referring to an animal that lives on or near the bottom of a body of water. Also an aquatic biome consisting of the ocean bottom below the pelagic and coastal zones. Bottom habitats in the very deepest oceans (below 9000 m) are sometimes referred to as the abyssal zone. see also oceanic vent.

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.

cosmopolitan

having a worldwide distribution. Found on all continents (except maybe Antarctica) and in all biogeographic provinces; or in all the major oceans (Atlantic, Indian, and Pacific.

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

The process by which an animal locates itself with respect to other animals and objects by emitting sound waves and sensing the pattern of the reflected sound waves.

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

fertilization

union of egg and spermatozoan

food

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

molluscivore

eats mollusks, members of Phylum Mollusca

motile

having the capacity to move from one place to another.

natatorial

specialized for swimming

nocturnal

active during the night

pelagic

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

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

social

associates with others of its species; forms social groups.

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).

tropical

the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.

visual

uses sight to communicate

viviparous

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

year-round breeding

breeding takes place throughout the year

young precocial

young are relatively well-developed when born

Ref­er­ences

2010. "NOAA fish­eries" (On-line). Of­fice of Pro­tected Re­sources. Ac­cessed March 12, 2011 at http://​www.​nmfs.​noaa.​gov/​pr/​species/​mammals/​cetaceans/​rissosdolphin.​htm.

Amano, M., N. Miyazaki. 2004. Com­po­si­tion of a school of Risso's dol­phins, Gram­pus griseus. Ma­rine and Fresh­wa­ter Bi­ol­ogy, Zo­ol­ogy, 20/1: 152-160.

Corkeron, P., S. Van Par­ijs. 2001. Vo­cal­iza­tions of eatern Aus­tail­ian Risso's dol­phins, Gram­pus griseus. Cana­dian Jour­nal of Zo­ol­ogy, 79/1: 160-164.

Culik, B. 2010. "Gram­pus griseus" (On-line). CMS (Con­ven­tion on Mi­gra­tory Spe­ices). Ac­cessed April 16, 2011 at http://​www.​cms.​int/​reports/​small_​cetaceans/​data/​g_​griseus/​g_​griseus.​htm.

Gas­pari, S., S. Airoldi, A. Hoelzel. 2007. Risso's dol­phins (Gram­pus griseus) in UK wa­ters are dif­fer­en­ti­ated from a pop­u­la­tion inte Mediter­ranean Sea and ge­net­i­cally less divers. Con­ser­va­tion Ge­net­ics, 8: 727-732.

Hart­man, K., F. Visser, A. Hen­driks. 2008. So­cial struc­ture of Risso's dol­phin (Gram­pus Griseus) at the Azores: a strat­i­fied com­mu­nity based on highly as­so­ci­ated so­cial units. Cana­dian Jour­nal of Zo­ol­ogy, 86/4: 294-306.

Jef­fer­son, T., S. Leather­wood, M. Web­ber. 1993. Ma­rine Mam­mals of the World. Rome: United Na­tions En­vi­ron­ment Pro­gramme. Ac­cessed March 31, 2011 at http://​books.​google.​com/​books?​id=W4Cbz0WphN0C&​printsec=frontcover&​cd=1&​source=gbs_​ViewAPI#​v=onepage&​q&​f=false.

Jef­fer­son, T., M. Web­ber, R. Pit­man. 2008. Ma­rine Mam­mals of the World, A Com­pre­hen­sive Guide to their Iden­ti­fi­ca­tion. San Diego, Cal­i­for­nia: El­se­vier. Ac­cessed March 12, 2011 at http://​books.​google.​com/​books?​id=TwFUimDtz7sC&​printsec=frontcover&​dq=Jefferson+Marine+mammals+of+the+world&​source=bl&​ots=B_​gBRRyj9B&​sig=KkGU24VxRGp6-Nzwapy63vJfXEs&​hl=en&​ei=Xmp-TabEIcLlrAHXnIXVBQ&​sa=X&​oi=book_​result&​ct=result&​resnum=3&​ved=0CCkQ6AEwAg#​v=onepage&​q&​f=false.

Kruse, S., D. Cald­well, M. Cald­well. 1999. Risso's Dol­phin. Pp. 183-212 in S Ridg­way, R Har­ri­son, eds. Hand­book of Ma­rine Mam­mals, Vol 6. Lon­don: Aca­d­e­mic Press.

Leather­wood, S., W. Per­rin, V. Kirby, C. Hubb, M. Dahlheim. 1980. Dis­tri­b­u­tion and move­ments of Risso's dol­phin, Gram­pus griseus, in the east­ern north Pa­cific. Fish­ery Bul­letin, 77/4: 951-963.

MacLeod, C. 1998. In­trasp­cific scar­ring in odon­to­cete cetaceans: and in­di­ca­tor of male 'qual­ity' in agres­sive so­cial in­ter­ac­tions?. Jour­nal of Zo­ol­ogy, 244: 71-77.

Mooney, T., P. Nachti­gall, M. Yuen. 2006. Tem­po­ral res­o­lu­tion of the Risso's dol­phin, Gram­pus griseus, au­di­tory sys­tem. Jour­nal of Com­par­a­tive Phys­i­o­log­i­cal Anatomy, 192: 373-380.

Nuno, J. 2008. Field Notes on the Risso's Dol­phin (Gram­pus Griseus) Dis­tri­b­u­tion, So­cial Ecol­ogy, Be­haious, and Oc­curence in the Azores. Aquatic Mam­mals, 34/4: 426.

Pawloski, J., P. Nachti­gall, W. Au, J. Philips, H. Roit­blat. 2003. Echolo­ca­tion in Risso's dol­phin, Gram­pus griseus. The Jour­nal of the Acousti­cal So­ci­ety of Amer­ica, 113/1: 605-616.

Raga, J., M. Rad­uan, C. Blanco. 2006. Diet of Risso's dol­phin (Gram­pus Griseus) in the west­ern Mediter­ranean Sea. Sci­en­tia Ma­rina, 70/3: 407-411.

Stew­art, B., P. Clapham, J. Pow­ell, R. Reeves. 2002. Na­tional Au­dobon's Guide to Ma­rine Mam­mals of the World. New York: Al­fred A. Knopf.

Storelli, M., G. Macrot­ri­giano. 2000. Per­sis­tent Or­ganchlo­rine Residues in Risso's Dol­phins (Gram­pus griseus) from the Mediter­ranean Sea. Ma­rine Pol­lu­tion Bul­letin, 40/6: 555-558.

Tay­lor, B., R. Baird, J. Bar­low, S. Daw­son, J. Ford, J. Mead, G. No­tar­bar­tolo di Sciara, P. Wade, R. Pit­man. 2010. "Gram­pus griseus" (On-line).

The IUCN Red List of Threat­ened Species
. Ac­cessed May 31, 2011 at http://​www.​iucnredlist.​org/​apps/​redlist/​details/​9461/​0.

Wur­sig, B., J. Thewis­sen. 2009. En­cy­clo­pe­dia of Ma­rine Mam­mals. Lon­don: Aca­d­e­mic.