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Lifespan, longevity, and ageing

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Maximum longevity: 18.4 years (wild)
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Biology

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The kitefin shark is a powerful deep-sea predator, feeding on a wide variety of bony fishes, skates, other sharks, cephalopods, crustaceans and worms (2) (3) (4) (6). Fish are the most commonly taken prey (2) (3), although the diet may vary seasonally, as well as with age (3). The kitefin shark is believed to be mainly solitary (2) (3), and reproduction is ovoviviparous, meaning the eggs develop and hatch inside the body, the female then giving birth to live young (2) (3) (4). Litter size varies from 10 to 16 pups, with each pup measuring around 30 centimetres long at birth (2) (3) (6). Little is known about the growth, lifespan, or age at maturity of the kitefin shark (6) (7).
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Conservation

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There are no specific conservation measures currently in place for the kitefin shark (6). It is a relatively poorly known species (7), and a lack of fisheries data and information on its abundance makes assessing its global conservation status difficult, leading to its current classification by the IUCN as Data Deficient (1) (2).
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Description

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A moderately sized shark with a short, blunt snout, the kitefin shark has two small, spineless dorsal fins, an asymmetrical caudal fin, with a well-developed notch near the tip, and no anal fin. The body is uniformly dark brown, greyish black or violet brown, often with poorly defined black spots on the upper surface, while the rounded fins have white or translucent edges, and the tail is tipped with black (2) (3) (4) (5). The 'lips' are thick and may be pale in colour, and the jaws are heavy, compact, and very powerful (2) (3) (5). The teeth of the kitefin shark differ greatly between the upper and lower jaws, being small, narrow and pointed in the upper jaw, and large, bladelike and serrated in the lower jaw (2) (3) (6). This species can sometimes be confused with the Portuguese shark, Centroscymnus coelolepis, but can be distinguished by the lack of spines on the dorsal fins (2).
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Habitat

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This deepwater species typically lives near, but not on, the sea bed. Most commonly found on continental and insular shelves and slopes in warm-temperate and tropical waters, the kitefin shark is most common below 200 metres, and has been recorded at depths of up to 1,800 metres (2) (3) (4) (6).
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Range

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The kitefin shark has a widespread but relatively patchy distribution (5) (6), being found in parts of the western and eastern Atlantic Ocean, the western Mediterranean, the western Indian Ocean, and the western and central Pacific Ocean (1) (2) (3) (4).
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Status

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Classified as Data Deficient (DD) on the IUCN Red List (1).
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Threats

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Although primarily caught as bycatch (2), and historically only the target of directed, deepwater line fisheries, commercial exploitation of kitefin sharks does occur in some areas, and is likely to increase in future as traditional fisheries decline and as deepwater fishing gear continues to develop (1) (6) (7). The species is sought mainly for its large, oily liver, which is rich in the compound squalene, and is also caught for food, leather, and to produce fishmeal (2) (3) (4) (6). However, the kitefin shark appears to have limited commercial potential, with rapid reduction in populations reported when large catches are taken (1) (6) (7) (8). The species is also likely to have low productivity, meaning that populations take a long time to recover after depletion (1) (2) (6).
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Diagnostic Description

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Moderately sized, short- and blunt-snouted shark with two almost equal-sized dorsal fins; papillose thick lips; small slender-cusped upper teeth and very large lower teeth with erect triangular serrated cusps and distal blades; first dorsal fin on back with its origin behind the pectoral rear tips and its base closer to the pectoral base than the pelvic fins; and caudal fin with the ventral lobe not expanded (Ref. 247). Dark grey-brown to black; trailing edges of fins translucent (Ref. 26346).
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Life Cycle

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Ovoviviparous (Ref. 247). 10-20 young born at 30-42 cm (Ref. 26346); 10-16 young born at 30 cm TL (Ref.58048). Distinct pairing with embrace (Ref. 205).
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Morphology

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Dorsal spines (total): 0; Dorsal soft rays (total): 0; Analspines: 0; Analsoft rays: 0
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Trophic Strategy

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Found on the continental shelf and slope (Ref. 75154). Feeds on fish and benthic organisms (Ref. 568).
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Biology

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Found on outer continental and insular shelves and slopes (Ref. 247). Mainly found on or near the bottom but readily occurs well off the substrate (Ref. 247, 58302). Often pelagic (Ref. 58302). Found singly or in small schools (Ref. 6871). Feeds mainly on deepwater bony fish, but also skates, other sharks (etmopterids in Ref. 123656), cephalopods and crustaceans (Ref. 5578). This bioluminiscent shark (currently the largest luminous vertebrate) emit light ventrally to counterilluminate which might be used to illuminate the ocean floor while searching/hunting for prey; or to stealthily approach prey, using counterillumination camouflage, before striking fast when it is close enough (Ref. 123656). Ovoviviparous (Ref. 205), with 10-20 young born at 30-42 cm (Ref. 26346). Used for its squalene liver oil, leather and meat, as well as for fishmeal (Ref. 6871).
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Importance

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fisheries: minor commercial; price category: medium; price reliability: reliable: based on ex-vessel price for this species
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分布

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廣泛分布於世界三大洋及地中海溫帶暖水域及熱帶水域。臺灣則分布於南部及東北部海域。
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臺灣魚類資料庫
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利用

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一般為底拖網捕獲,全身皆被利用,包括魚皮、魚肉及魚肝魚等。
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描述

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體頗長,圓柱形;吻甚短,眼前吻長約等於眼徑;眼卵圓形,眼徑為口前吻長的1/2;噴水孔位於眼睛後上方,孔徑為眼徑的1/2;口裂淺弧形,口寬約等於或稍大於口前吻長;唇厚,肉質;上下顎齒不同形,上顎齒尖刺狀,基底寬,有二叉,正中齒直立,兩側齒向口角後方漸傾斜,每側8-9枚;下顎齒每側8-9枚,葉片狀,基底扁方形,與相鄰齒相互重疊,齒冠三角形,具鋸齒緣,正中齒直立,兩側齒向口角後方漸傾斜,齒亦漸小;上顎齒3-4行,下顎齒1-2行在使用;鰓裂五對,小於眼徑,最後一個稍大;盾鱗具一棘突,排列稀疏,彼此不重疊。背鰭二個,較小;第一背鰭上角圓,後緣直;第二背鰭大於第一背鰭,起點約在腹鰭基底後方1/3的上方,內緣長約等於基底長;尾鰭上葉發達,下葉前與上葉相接處有一缺刻;腹鰭基底約為第二背鰭基底長的1.5倍,前緣直,角圓,後角尖突;胸鰭外角圓,後緣圓突,內角圓弧形。
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棲地

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生活於溫帶、熱帶大陸棚和島嶼斜坡水域之底層深水鯊,分布於37公尺到至少1800公尺深處,但常見於200公尺附近水深處。肝臟含油量高,可增加浮力,不用鰭或身體擺動即可停在水中。不成群,常單獨行動。卵胎生,每產10-16子,剛產子鯊長約30公分。主要以底棲硬骨魚為食,但也捕食魟、鮫、頭足類及甲殼類等。
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Kitefin shark

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The kitefin shark or seal shark (Dalatias licha) is a species of squaliform shark in the family Dalatiidae, and the type species in its genus. It is found sporadically around the world, usually close to the sea floor at depths of 200–600 m (660–1,970 ft). With a sizable oil-filled liver to maintain neutral buoyancy, this shark is able to cruise slowly through the water while expending little energy. The kitefin shark, the largest luminous vertebrate on record,[3] has a slender body with a very short, blunt snout, large eyes, and thick lips. Its teeth are highly differentiated between the upper and lower jaws, with the upper teeth small and narrow and the lower teeth large, triangular, and serrated. Its typical length is 1.0–1.4 m (3.3–4.6 ft), though examples as long as 5.9 ft (180 cm) have been encountered.[3]

Armed with large teeth and a strong bite, the kitefin shark is a powerful, solitary predator that takes many different types of prey, ranging from bony fishes, sharks and rays, to cephalopods, crustaceans, polychaete worms, siphonophores, and possibly carrion. It also takes bites out of animals larger than itself, similar to its smaller relative, the cookiecutter shark (Isistius brasiliensis). This shark is aplacental viviparous and gives birth to 10–14 young. The kitefin shark is fished commercially for its meat, skin, and liver oil, primarily by Portugal and Japan. A fishery targeting this species existed off the Azores from the 1970s to the 1990s, but collapsed due to overfishing and falling liver oil prices; the rapid depletion of the Azores stock is often cited as an example of the susceptibility of deep-sea sharks to human exploitation. The low reproductive rate of this species renders it susceptible to overfishing and, coupled with known population declines, has led it to be assessed as Vulnerable by the International Union for Conservation of Nature (IUCN).

Taxonomy

The kitefin shark was originally described as Squalus licha by French naturalist Pierre Joseph Bonnaterre, in his 1788 Tableau encyclopédique et méthodique des trois regnes de la nature; the type specimen from "Le cap Breton" has since been lost. This species was later placed in its own genus, Dalatias, which came from the synonymy of Constantine Rafinesque's 1810 Dalatias sparophagus with S. licha. However, some authorities dispute this on the grounds that D. sparophagus is a nomen dubium, and prefer to use the next available genus name Scymnorhinus.[4] The genus name Dalatias is derived from the Greek dalos or dalou, meaning "torch".[5] The specific epithet licha comes from liche, the French name for this shark (from Occitan lecha, from lec, "glutton").[6][7] Additional common names used for the kitefin shark include black shark and darkie Charlie.[5]

Phylogeny and evolution

Cladistic studies have consistently found that the closest relatives of the kitefin shark are the cookiecutter sharks (Isistius), with which they share several dentitional, skeletal, and muscular similarities.[8][9] Dalatias and Isistius are believed to have evolutionarily diverged shortly after the transition between the Cretaceous and Tertiary periods (65.5 Ma), as part of a larger adaptive radiation of dogfish sharks from the deep sea into relatively shallower habitats.[8]

The oldest fossil teeth that definitively belong to the kitefin shark date to the Middle Eocene epoch, such as those recovered from Bortonian-stage deposits (43.0–37.0 Ma) in New Zealand.[1] Dalatias fossil teeth dating to various ages have also been discovered in Europe, the former USSR, Japan, and western India.[10] The fossil material now recognized as belonging to this species were historically described under a multitude of different names.[1]

Description

The head of a kitefin shark, showing the large eyes, stubby snout, and thick lips

The kitefin shark has a moderately elongated body with a very short, rounded snout. The eyes and spiracles are large. The lips are thick with pleats or fringes, though are not modified to be suctorial. There are 16–21 tooth rows in the upper jaw and 17–20 tooth rows in the lower jaw.[4] The upper teeth are small and spike-shaped, curving slightly towards the corners of the mouth. The lower teeth are very large, knife-shaped, and serrated, with their bases interlocking to form a continuous cutting surface.[11]

The first dorsal fin is slightly smaller and shorter-based than the second, and neither has spines. The first dorsal fin originates behind the free rear tip of the pectoral fins, while the second originates above the middle of the pelvic fin bases. The pectoral fins are short and rounded. The caudal fin has a prominent upper lobe with a well-developed notch near the tip, and a barely present lower lobe.[4] The form and arrangement of the fins is similar to the Portuguese dogfish (Centroscymnus coelolepis), from which this species can be distinguished by the lack of fin spines.[11] The dermal denticles are small and flat, with a single horizontal ridge ending in a point.[4]

The coloration is a uniform dark brown or gray, sometimes with faint black spots on the back. The fins have white or translucent trailing edges,[12] and the tip of the caudal fin is black.[11] An 90 cm (3.0 ft) long kitefin shark with partial albinism, lacking pigment on 59% of its body, was caught in the Gulf of Genoa in 2003. Unlike in a previous case of an albino Portuguese dogfish, the abnormal coloration of this individual had not diminished its ability to capture prey.[13] Most kitefin sharks are 1.0–1.4 m (3.3–4.6 ft) long and weigh 8 kg (18 lb); the maximum reported length is 1.6 m (5.2 ft), possibly 1.8 m (5.9 ft).[11][14]

The kitefin shark is the largest known shark that exhibits bioluminesce.[15] The light is generated by photophores that consist of a single photocyte within in a cup-shaped pigmented cell, with lens cells on the surface. The bioluminesence is directed downwards from its front or belly. There are two hypotheses for the use of bioluminesence by D. licha; either it illuminates the sea floor while the shark is searching for prey, or it is used as a counter-illumination camouflage when approaching prey.[16]

Distribution and habitat

The kitefin shark has an almost circumglobal range in tropical and warm-temperature waters, consisting of a number of widely separated populations with likely little interchange between them.[17] This shark has not been reported from the eastern Pacific and northern Indian Oceans. In the northern Atlantic, it occurs in the Georges Bank and the northern Gulf of Mexico, and from the North Sea to Cameroon, including around the British Isles, in the western and central Mediterranean Sea, and off Madeira and the Azores. In the Indian Ocean, it is found off South Africa and Mozambique. In the Pacific, it occurs off Japan, Java, Australia and New Zealand, and the Hawaiian Islands. There is a single record of this species in the southern Atlantic, from off southern Brazil.[2][4][18]

An offshore, deepwater species, the kitefin shark is most common at a depth of 200–600 m (660–1,970 ft), but has been captured from the surface to as deep as 1,800 m (5,900 ft).[11][18] Off the Azores this shark segregates by sex, with females most common around a depth of 230 m (750 ft) and males most common around 412–448 m (1,352–1,470 ft).[14] The kitefin shark inhabits the outer continental shelves and upper continental slopes, and is also found around oceanic islands and seamounts.[10] It is the only member of its family that tends to be found close to the sea floor as opposed to in the middle of the water column, though on occasion it has been captured well above the bottom.[10]

Biology and ecology

The lower teeth of the kitefin shark form a continuous cutting edge, enabling it to take bites out of larger animals.

Relatively common where it occurs, kitefin sharks are usually solitary in nature but may form small groups.[18] It is a slow swimmer with a large liver filled with squalene, a lipid less dense than water, allowing it to maintain neutral buoyancy and hover above the bottom with little effort.[4] Studies off the coast of North Africa and in the Gulf of Genoa have found males outnumbering females by 2:1 and 5:1 respectively; this imbalanced sex ratio has not been observed off South Africa and may reflect sampling bias.[19] The kitefin shark is preyed upon by larger fishes and sharks,[11] as well as by sperm whales (Physeter macrocephalus).[20] Parasite data on this species is limited; an examination of two sharks caught off Ireland found three nematodes in the stomach lumen. One could be identified as Anisakis simplex L3, while another may have been a larval Raphidascaris.[21]

A powerful and versatile deepwater predator, the short, robust jaws of the kitefin shark give it an enormously strong bite. It feeds mainly on bony fishes (including deepwater smelts, viperfishes, scaly dragonfishes, barracudinas, greeneyes, lanternfishes, bristlemouths, cod and other gadids, grenadiers, deepwater scorpionfishes, bonito, snake mackerels, deepwater cardinalfishes, and sea toads), but also takes a wide variety of other animals, including skates, smaller sharks (Galeus, Squalus, Etmopterus and Centrophorus), squid and octopus, crustaceans (amphipods, isopods, shrimp and lobsters), polychaete worms, and siphonophores.[4] Like the related cookiecutter shark, the kitefin shark is also capable of excising chunks of flesh from animals larger than itself, including other sharks and whales.[18][22] The presence of fast-swimming fishes in its diet suggests the kitefin shark may scavenge, or have some other means of capturing faster prey. In the Mediterranean, bony fishes are the most important food year-round, with the second-most important prey being sharks in the winter and spring, crustaceans in the summer, and cephalopods in the fall. Captured males are more likely to have full stomachs than females for unknown reasons.[4]

Reproduction in the kitefin shark is aplacental viviparous, with the embryos hatching inside the uterus and being sustained to term by yolk. Adult females have two functional ovaries and two functional uteruses; the uterus is not divided into compartments. In the Mediterranean, breeding occurs throughout the year with peaks in spring and fall; females may have a year of rest in between pregnancies.[2][19] The litter size is 10–16, increasing with female size.[17] The young are born at a length of 30–45 cm (12–18 in), varying by geographic location, after a possible gestation period of two years.[14][23] The males mature sexually at a length of 77–121 cm (2.53–3.97 ft), and the females at a length of 117–159 cm (3.84–5.22 ft).[17] There is no relationship between an individual's size at birth, size at maturity, and maximum size.[19]

Human interactions

Japanese researchers measure a kitefin shark; this species has long been of economic significance.

The kitefin shark inhabits depths too great for it to be a danger to humans.[11] Its upper teeth have been found lodged in underwater fiberoptic cables.[22] This species has a long history of human exploitation: the meat is consumed in the eastern Atlantic and Japan, and the offal processed into fishmeal. The liver oil is utilized in Portugal, Japan, and South Africa. The skin is made into a type of shagreen useful in the making of furniture and jewelry, and is also favored for the manufacture of "boroso", a Spanish polished leather. This shark has no commercial value in the western Atlantic.[11][17]

The continuing expansion of commercial fisheries into the deep sea has raised concerns about the vulnerability of this and other deepwater shark species to overfishing, as these sharks have slow growth and reproductive rates. This is exemplified by the rapid stock depletion and collapse of the Azores kitefin shark fishery.[2] This targeted fishery began in the early 1970s for the production of liver oil. In the early 1980s, the fishing fleet was enlarged with the addition of industrial vessels equipped with demersal gillnets, resulting in a fishery peak in 1984 of 937 tons landed. After 1991, kitefin shark catches declined precipitously to under 15 tons annually which, along with a drop in the global price of liver oil, led to the fishery becoming unprofitable by the end of the decade. A population assessment has suggested that the northeastern Atlantic stock had fallen to 50% of the pre-exploitation biomass.[24][25]

Fisheries operating off Portugal and Japan are responsible for most commercial landings of the kitefin shark, generally as bycatch in bottom trawls and on hook-and-line.[11][26] Portugal reported a kitefin shark bycatch of 282 tons in 2000 and 119 tons in 2003. In other areas of the northeastern Atlantic this shark is rare and reported catches are likely confounded by misidentifications of other species; some are caught by mixed-species gillnet fisheries operating in deep water west of the British Isles, where surveys suggest that kitefin shark numbers may have declined by 94% since the 1970s.[2][24] In the Mediterranean, this shark is caught incidentally by bottom trawl and gillnet fisheries. Although it is generally discarded alive, many are unable to return to deep water and do not survive.[2] In the Southern Hemisphere, catches by the Australian South East Trawl Fishery are increasing following the relaxation of regulations regarding seafood mercury content; this species is not included under Australian fishery quotas.[11] New Zealand kitefin shark catches peaked from 1986 to 1997.[25] In June 2018 the New Zealand Department of Conservation classified the kitefin shark as "Not Threatened" with the qualifier "Secure Overseas" under the New Zealand Threat Classification System.[27] The International Union for Conservation of Nature has assessed the kitefin shark as a vulnerable species in light of documented population declines.[2]

See also

References

  1. ^ a b c Keyes, I.W. (1984). "New records of fossil elasmobranch genera Megascyliorhinus, Centrophorus, and Dalatias (Order Selachii) in New Zealand". New Zealand Journal of Geology and Geophysics. 27 (2): 203–216. doi:10.1080/00288306.1984.10422527.
  2. ^ a b c d e f g Finucci, B.; Walls, R.H.L.; Guallart, J.; Kyne, P.M. (2018). "Dalatias licha". IUCN Red List of Threatened Species. 2018: e.T6229A3111662. doi:10.2305/IUCN.UK.2018-2.RLTS.T6229A3111662.en. Retrieved 19 November 2021.
  3. ^ a b Hunt, Elle (2 March 2021). "Giant luminous shark': researchers discover three deep-sea sharks glow in the dark". The Guardian.
  4. ^ a b c d e f g h Compagno, L.J.V. (1984). Sharks of the World: An Annotated and Illustrated Catalogue of Shark Species Known to Date (PDF). Rome: Food and Agricultural Organization. pp. 63–64. ISBN 978-92-5-101384-7.
  5. ^ a b Froese, Rainer; Pauly, Daniel (eds.) (2009). "Dalatias licha" in FishBase. June 2009 version.
  6. ^ "L'Occitan de Comunicason - Dictionnaire Français - Occitan".
  7. ^ Bonnaterre, P.J. (1788). Tableau encyclopédique et méthodique des trois regnes de la nature. Chez Panckoucke. p. 12.
  8. ^ a b Adnet, S.; Cappetta, H. (September 2001). "A palaeontological and phylogenetical analysis of squaliform sharks (Chondrichthyes: Squaliformes) based on dental characters". Lethaia. 34 (3): 234–248. doi:10.1080/002411601316981188.
  9. ^ Shirai, S. (1996). "Phylogenetic Interrelationships of Neoselachians (Chondrichthyes: Euselachii)". In Stiassny, M.L.J.; Parenti, L.R.; Johnson, G.D. (eds.). Interrelationships of Fishes. Academic Press. pp. 9–34. ISBN 978-0-12-670950-6.
  10. ^ a b c Carrier, J.C.; Musick, J.A.; Heithaus, M.R. (2004). Biology of Sharks and Their Relatives. CRC Press. p. 58. ISBN 978-0-8493-1514-5.
  11. ^ a b c d e f g h i j Bester, C. and Burgess, G. Biological Profiles: Kitefin Shark. Florida Museum of Natural History Ichthyology Department. Retrieved on June 15, 2009.
  12. ^ Dianne J. Bray & William T. White, 2011, Black Shark, Dalatias licha, in Fishes of Australia, accessed 25 Aug 2014, http://www.fishesofaustralia.net.au/Home/species/2008 Archived 2014-08-26 at the Wayback Machine
  13. ^ Bottaro, M., Ferrando, S., Gallus, L., Girosi, L. and Vacchi, M. (2005). "First record of albinism in the deep water shark Dalatias licha" Archived 2006-09-25 at the Wayback Machine Reference No. 5115. JMBA2–Biodiversity Records.
  14. ^ a b c Kiraly, S.J.; J.A. Moore; P.H. Jasinski (2003). "Deepwater and Other Sharks of the U.S. Atlantic Ocean Exclusive Economic Zone". Marine Fisheries Review. 65 (4): 1–63.
  15. ^ 'Giant luminous shark': researchers discover three deep-sea sharks glow in the dark , The Guardian, 2 Mar 2021
  16. ^ Jerome Mallefet; Darren W. Stevens; Laurent Duchatelet (26 February 2021). "Bioluminescence of the Largest Luminous Vertebrate, the Kitefin Shark, Dalatias licha: First Insights and Comparative Aspects". Frontiers in Marine Science. 8. doi:10.3389/FMARS.2021.633582. ISSN 2296-7745. Wikidata Q112807357.
  17. ^ a b c d Fowler, S.L.; Cavanagh, R.D.; Camhi, M.; Burgess, G.H.; Cailliet, G.M.; Fordham, S.V.; Simpfendorfer, C.A.; Musick, J.A. (2005). Sharks, Rays and Chimaeras: The Status of the Chondrichthyan Fishes. International Union for Conservation of Nature and Natural Resources. pp. 230–231. ISBN 978-2-8317-0700-6.
  18. ^ a b c d Soto, J.M.R.; Mincarone, M.M. (2001). "First record of kitefin shark, Dalatias licha (Bonnaterre, 1788) (Chondrichthyes, Dalatiidae), in the south Atlantic". Mare Magnun. 1 (1): 23–26.
  19. ^ a b c Capapé, C.; Hemida, F.; Quignard, J.P. (2008). "Biological observations on a rare deep-sea shark, Dalatias licha (Chondrichthyes: Dalatiidae), off the Maghreb coast (south-western Mediterranean)". Pan-American Journal of Aquatic Sciences. 3 (3): 355–360.
  20. ^ Gómez-Villota, F. (2007). Sperm whale diet in New Zealand. Master of Applied Science thesis. Auckland University of Technology.
  21. ^ Henderson, A.C.; Flannery, K.; Dunne, J. (2003). "Biological observations on shark species taken in commercial fisheries to the west of Ireland". Biology and Environment. 103B: 1–7. doi:10.1353/bae.2003.0022.
  22. ^ a b Musick, J.A.; McMillan B. (2003). The Shark Chronicles: A Scientist Tracks the Consummate Predator. Macmillan. pp. 122–123. ISBN 978-0-8050-7359-1.
  23. ^ da Silva, H.M. (1988). "Growth and reproduction of kitefin shark, Dalatias licha (Bonn 1788) in Azorean waters." ICES, Demersal Fish Committee CM 1988/G:21. pp. 1–16.
  24. ^ a b ICES. (2007). Report of the Working Group Elasmobranch Fishes (WGEF), 22–28 June 2007, Galway, Ireland. Archived 12 June 2011 at the Wayback Machine ICES CM 2007/ACFM:27. pp. 52–55.
  25. ^ a b Perrotta, R. (2004). "Kitefin shark, Dalatias licha (dalatiidae) fishery in the north eastern Atlantic and some recommendations for elasmobranchs exploitation". Revista de Investigación y Desarollo Pesquero. 16: 97–101.
  26. ^ Castro, J.I., Woodley, C.M. and Brudek, R.L. (1999). A preliminary evaluation of the status of shark species. FAO Fisheries Technical Paper No. 380.
  27. ^ Duffy, Clinton A. J.; Francis, Malcolm; Dunn, M. R.; Finucci, Brit; Ford, Richard; Hitchmough, Rod; Rolfe, Jeremy (2018). Conservation status of New Zealand chondrichthyans (chimaeras, sharks and rays), 2016 (PDF). Wellington, New Zealand: Department of Conservation. p. 10. ISBN 9781988514628. OCLC 1042901090.

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Kitefin shark: Brief Summary

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The kitefin shark or seal shark (Dalatias licha) is a species of squaliform shark in the family Dalatiidae, and the type species in its genus. It is found sporadically around the world, usually close to the sea floor at depths of 200–600 m (660–1,970 ft). With a sizable oil-filled liver to maintain neutral buoyancy, this shark is able to cruise slowly through the water while expending little energy. The kitefin shark, the largest luminous vertebrate on record, has a slender body with a very short, blunt snout, large eyes, and thick lips. Its teeth are highly differentiated between the upper and lower jaws, with the upper teeth small and narrow and the lower teeth large, triangular, and serrated. Its typical length is 1.0–1.4 m (3.3–4.6 ft), though examples as long as 5.9 ft (180 cm) have been encountered.

Armed with large teeth and a strong bite, the kitefin shark is a powerful, solitary predator that takes many different types of prey, ranging from bony fishes, sharks and rays, to cephalopods, crustaceans, polychaete worms, siphonophores, and possibly carrion. It also takes bites out of animals larger than itself, similar to its smaller relative, the cookiecutter shark (Isistius brasiliensis). This shark is aplacental viviparous and gives birth to 10–14 young. The kitefin shark is fished commercially for its meat, skin, and liver oil, primarily by Portugal and Japan. A fishery targeting this species existed off the Azores from the 1970s to the 1990s, but collapsed due to overfishing and falling liver oil prices; the rapid depletion of the Azores stock is often cited as an example of the susceptibility of deep-sea sharks to human exploitation. The low reproductive rate of this species renders it susceptible to overfishing and, coupled with known population declines, has led it to be assessed as Vulnerable by the International Union for Conservation of Nature (IUCN).

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Description

provided by World Register of Marine Species
Found on the outer continental and insular shelves and slopes, most commonly below 200 m. Primarily a solitary shark. Feeds mainly on bony fishes and also skates, other sharks (Galeus, Squalus, Etmopterus and Centrophorus), and also on squids, octopi, amphipods, isopods, shrimps, lobsters, polychaetes and siphonophores. Adults eat more crustaceans and sharks and less cephalopods than young. Ovoviviparous with 10 to 16 young in a litter. Quite common.

Reference

Froese, R. & D. Pauly (Editors). (2023). FishBase. World Wide Web electronic publication. version (02/2023).

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Distribution

provided by World Register of Marine Species
from George's Bank, the east coast of Florida, Northern Gulf of Mexico, and off the southern Bahamas

Reference

North-West Atlantic Ocean species (NWARMS)

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Habitat

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benthic

Reference

North-West Atlantic Ocean species (NWARMS)

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Habitat

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Known from seamounts and knolls

Reference

Stocks, K. 2009. Seamounts Online: an online information system for seamount biology. Version 2009-1. World Wide Web electronic publication.

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