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Lifespan, longevity, and ageing

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Maximum longevity: 30 years (wild)
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Life Cycle

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Porbeagle embryos are oophagous, feeding on eggs produced by the ovaries. Females retain eggs in a brooding chamber, where embryos develop while receiving nourishment from the yolk sac. Embryos develop in egg cases, also known as mermaid's purses. Once development is complete, young hatch while inside the mother's uterus and parturition is complete. Gestation lasts 8 to 9 months. Upon birth, pups are 60 to 75 cm long and weigh about 9 kg. Most males become reproductively mature by 1.5 to 2.0 m in length and 130 kg in mass, or by 8 years of age. Females reach maturity by 2.0 to 2.5 m in length and 200 kg in mass, or by 13 years of age.

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Edmunds, J. and R. Meredith 2011. "Lamna nasus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Lamna_nasus.html
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John Edmunds, Radford University
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Richard Meredith, Radford University
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Gregory Zagursky, Radford University
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John Berini, Special Projects
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Associations

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There is no information available regarding predators specific to porbeagles. White sharks and orcas have been suggested as possible predators, however, there is no evidence to support this idea.

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Edmunds, J. and R. Meredith 2011. "Lamna nasus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Lamna_nasus.html
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John Edmunds, Radford University
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Richard Meredith, Radford University
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Gregory Zagursky, Radford University
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John Berini, Special Projects
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Morphology

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While the dorsal and lateral surface of porbeagles is blue-gray, the venter is typically white. Pups may have dark patches on the ventral surface of the pectoral fins and near the underside of the gill slits. The tip of the dorsal fin is completely blue-gray, which differentiates them from salmon sharks and white sharks. Porbeagles have heavy fusiform bodies with large gill slits. They have crescent-shaped tails, long conical snouts and the anal and second dorsal fins can pivot. Their teeth have lateral cusplets and are large and bladelike with smooth edges, unlike those of white sharks, which are often serrated. Like most sharks, adult porbeagles have dermal denticles, however, pups often lack them. Their maximum length and weight are approximately 365 cm and 230 kg, respectively, females are slightly larger than males. Female in the northern hemisphere range from 232 to 259 cm in length, and females in the southern hemisphere range from 185 to 202 cm in length. Males do not exhibit geographic variation in size and range from 165 to 207 cm in length. Pups range from 60 to 75 cm in length at birth. The average weight of porbeagles is 135 kg. Unlike most fish, porbeagles are endothermic.

Range mass: 230 (high) kg.

Average mass: 135 kg.

Range length: 165 to 365 cm.

Other Physical Features: endothermic ; bilateral symmetry

Sexual Dimorphism: female larger

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Edmunds, J. and R. Meredith 2011. "Lamna nasus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Lamna_nasus.html
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John Edmunds, Radford University
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Richard Meredith, Radford University
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Gregory Zagursky, Radford University
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John Berini, Special Projects
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Life Expectancy

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Porbeagles live between 25 and 46 years in the wild.

Range lifespan
Status: wild:
25 to 46 years.

Average lifespan
Status: wild:
30 years.

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Edmunds, J. and R. Meredith 2011. "Lamna nasus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Lamna_nasus.html
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John Edmunds, Radford University
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Richard Meredith, Radford University
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Gregory Zagursky, Radford University
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John Berini, Special Projects
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Habitat

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Porbeagles, a species of mackerel shark, are primarily found in the pelagic and littoral zones and prefer cold, offshore fishing banks. They seldom come inshore and are commonly found swimming along Reykjanes Ridge in the North Atlantic. They have also been found in brackish waters off the coast of Argentina. They often remain in deeper waters during winter and occasionally come inshore during summer. Although they have been documented in waters as deep as 1360 m, average depth of porbeagle inhabited waters is 715 m. Preferred water temperatures range from 1°C to 18°C.

Range depth: 1360 (high) m.

Average depth: 715 m.

Habitat Regions: saltwater or marine

Aquatic Biomes: pelagic ; oceanic vent ; coastal ; brackish water

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Edmunds, J. and R. Meredith 2011. "Lamna nasus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Lamna_nasus.html
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John Edmunds, Radford University
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Richard Meredith, Radford University
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Gregory Zagursky, Radford University
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John Berini, Special Projects
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Distribution

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Porbeagles (Lamna nasus) can be found in the northern hemisphere of the Atlantic Ocean, from South Carolina in the United States to as far north as the southern edge of Svalbard, Norway. Porbeagles are also found in the Mediterranean Sea and from Morocco to the arctic waters off the northwestern coast Russia. In the southern Hemisphere, they can be found in a band between 30 and 60 degrees south, primarily along the southern, eastern and western coasts of South America, Africa, and Australia.

Biogeographic Regions: nearctic (Native ); palearctic (Native ); ethiopian (Native ); neotropical ; australian (Native ); arctic ocean (Native ); atlantic ocean (Native ); pacific ocean (Native ); mediterranean sea (Native )

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Edmunds, J. and R. Meredith 2011. "Lamna nasus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Lamna_nasus.html
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John Edmunds, Radford University
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Richard Meredith, Radford University
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Gregory Zagursky, Radford University
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John Berini, Special Projects
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Trophic Strategy

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Porbeagles prey upon a variety of pelagic fishes including lancetfish, herring, sardines or pilchards, sauries, and mackerel. Secondary prey includes cusk, cod, redfish (i.e., Sebastes, Lutjanus, Trachichthyidae and Berycidae), haddock, squid, lumpsuckers, sandlances, flounders (Achiridae and Bothidae), and shellfish. Occasionally they may feed on other sharks such as tope and spiny dogfish. Porbeagles have also been documented consuming sea snails and sea urchins, which suggests they may forage at the bottom of the water column. Porbeagles have not been documented eating marine mammals. About 90% of the diet of porbeagles resident to the northwest Atlantic consists of bony fishes. Although they are considered to be opportunistic feeders, porbeagles prefer pelagic fish in the spring and groundfish in the fall.

Animal Foods: fish; mollusks; echinoderms

Primary Diet: carnivore (Piscivore )

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Edmunds, J. and R. Meredith 2011. "Lamna nasus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Lamna_nasus.html
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John Edmunds, Radford University
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Richard Meredith, Radford University
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Gregory Zagursky, Radford University
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John Berini, Special Projects
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Associations

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Porbeagles are important primary and secondary consumers of a number of marine animals and are considered a keystone species in their environment. As a result, porbeagles help maintain and regulate the abundance and distribution of numerous species, and thus help mediate the balance of their ecosystem. Little else is know of the potential ecosystem roles filled by porbeagles.

Ecosystem Impact: keystone species

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Edmunds, J. and R. Meredith 2011. "Lamna nasus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Lamna_nasus.html
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John Edmunds, Radford University
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Richard Meredith, Radford University
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Gregory Zagursky, Radford University
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John Berini, Special Projects
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Benefits

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Porbeagles are commonly sold in fish markets across the globe. Specifically, their fins are used for shark-fin soup. Porbeagles are also used for liver oil and to make fishmeal. In the 1960's, fisheries caught over nine million pounds of porbeagle annually. Porbeagles are also considered an important game fish throughout their geographic range.

Positive Impacts: food ; body parts are source of valuable material

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Edmunds, J. and R. Meredith 2011. "Lamna nasus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Lamna_nasus.html
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John Edmunds, Radford University
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Richard Meredith, Radford University
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Gregory Zagursky, Radford University
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John Berini, Special Projects
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Benefits

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The porbeagle Lamna nasus is a relatively large species and could be concidered dangerous as a result. The International Shark Attack File (ISAF) has only three probeagle attacks on record, however, these reports are not entirely reliable as porbeagles are often misidentified as white sharks.

Negative Impacts: injures humans (bites or stings)

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Edmunds, J. and R. Meredith 2011. "Lamna nasus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Lamna_nasus.html
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John Edmunds, Radford University
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Richard Meredith, Radford University
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Gregory Zagursky, Radford University
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John Berini, Special Projects
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Conservation Status

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Porbeagles are classified as vulnerable on the IUCN's Red List of Threatened Species. The blogal population of porbeagles is currently in decline and major threats vary by location. From 1998 to 1999, only 15 specimens were caught in the Mediterranean Sea as a result of by-catch and it appears that by-catch is their biggest threat in this region. In the northwest Atlantic, overfishing has lead to their decline, and in the southern oceans, it appears that by-catch on longlines has lead to significant declines throughout the southern limits of their geographic range.

IUCN Red List of Threatened Species: vulnerable

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Edmunds, J. and R. Meredith 2011. "Lamna nasus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Lamna_nasus.html
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John Edmunds, Radford University
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Richard Meredith, Radford University
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Gregory Zagursky, Radford University
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John Berini, Special Projects
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Behavior

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Male porbeagles communicate with females by biting their pectoral fins, letting the female know he wants to mate. Porbeagles are one of a few shark species that exhibit playful behavior. They have been observed alone, and in groups, playing with floating objects. Like other sharks, porbeagles possess Ampullae of Lorenzini, a series of electroreceptors that allows sharks to detect electrical fields. This electrosensory system likely helps them detect electrical pulses created via muscle contractions of prey and has been hypothesized to help them detect minor changes in temperature and pressure in the local environment. Porbeagles also perceive their local environment via the lateral line system common in most fish. The lateral line system helps them detect movement and vibrations in the surrounding environment. In conjunction with the Ampullae of Lorenzini, the lateral line system has helped sharks become extremely efficient and adept predators.

Communication Channels: tactile

Perception Channels: visual ; acoustic ; chemical ; electric

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Edmunds, J. and R. Meredith 2011. "Lamna nasus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Lamna_nasus.html
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John Edmunds, Radford University
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Richard Meredith, Radford University
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Gregory Zagursky, Radford University
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John Berini, Special Projects
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Reproduction

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Porbeagles are polygynandrous and mate from September to November. There are two mating grounds for western North Atlantic populations; one of which is off the coast of Newfoundland and the other is on Georges Bank in the Gulf of Maine. Prior to mating, males often bite their mate's pectoral fins and flanks in order to remain stable during copulation. Porbeagles breed once a year.

Mating System: polygynandrous (promiscuous)

Porbeagles are ovoviviparous (retaining eggs within the body until they hatch) and breed from September to November. Although North Atlantic populations breed throughout the eastern and western regions of their habitat, most copulation sightings have occurred along the north eastern coast of the United States, in the Gulf of Maine and off the coast of Newfoundland, Canada. Porbeagles are oophagous, as developing embryos feed on fertilized eggs to get nutrients once the yolk sac is depleted. Females give birth to between 1 and 5 pups during late winter and spring, with an average of 4 pups per litter. Pups are usually 60 to 75 cm long at birth and do not exceed 5 kg. Gestation lasts 8 to 9 months. Most males are reproductively mature by age 8, and most females are reproductively mature by age 13.

Breeding interval: Porbeagles breed once a year

Breeding season: Porbeagles breed from September to November.

Range number of offspring: 1 to 5.

Average number of offspring: 4.

Range gestation period: 8 to 9 months.

Average age at sexual or reproductive maturity (female): 13 years.

Average age at sexual or reproductive maturity (male): 8 years.

Key Reproductive Features: seasonal breeding ; sexual ; fertilization (Internal ); ovoviviparous

There is no information regarding parental care in porbeagles. In general, however, shark mothers provide a great deal of care to their pups. Sharks mature more slowly than other many other vertebrates, which increases demand for parental investment if young are to survive to reproductive maturity. Parental care by male sharks is uncommon and has not been documented in porbeagles.

Parental Investment: female parental care

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Edmunds, J. and R. Meredith 2011. "Lamna nasus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Lamna_nasus.html
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John Edmunds, Radford University
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Richard Meredith, Radford University
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Gregory Zagursky, Radford University
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John Berini, Special Projects
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Biology

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This active shark wanders about the ocean, often aggregating in small schools (2). It is an opportunistic hunter that swims strongly in pursuit of prey, and on calm days their triangular dorsal fin followed by the tip of the caudal fin can be seen cutting through the waters' surface (4). It feeds primarily on a wide range of bony fish such as mackerel, hake, herring and haddock, but cephalopods, such as squid and cuttlefish, are also consumed (2) (3). The porbeagle has been known to annoy fishermen by scavenging cod and other fish from longlines (4). When porbeagles mate, the male bites the female to hold her in place while they copulate (3). They are ovoviviparous sharks, and thus embryos develop within the female's uterus without forming a placental connection. Instead, the foetuses obtain nutrition by feeding on fertilised eggs within the uterus (2) (4). They possess fang-like teeth to tear open the egg capsules (2), and their stomachs become greatly swollen by feeding on the masses of yolk (2) (4). The gestation period is thought last for about eight or nine months, with litters of one to five pups born in the spring and summer in the northern hemisphere, or between April and September in the southern hemisphere (2).
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Conservation

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Catches of porbeagle are regulated by the European Community, which permits only a small regulated catch for Norway and New Zealand (3). In Canada, a porbeagle shark management plan was developed in the 1990's (5), which includes measures such as limited fishing licenses, gear, fishing areas and seasons for the porbeagle (3). However, it is uncertain whether these measures to reduce exploitation are sufficient to allow for recovery of the northwest Atlantic population (5). In the United States the porbeagle is currently included in the Highly Migratory Species Fishery Management Plan, and there is an annual quota in place. Except for the New Zealand fishery, there is no regulation on catches of the porbeagle in the southern hemisphere (3). At present, there is also no regulation of the international trade demand for meat that is driving many fisheries (1). In June 2007, at the meeting of the Conference of CITES Parties in June 2007, a proposal was raised to list the porbeagle under Appendix II, which would mean that trade in this species would be controlled in order to ensure it was compatible with their survival. Unfortunately, the proposal fell short of the votes needed to adopt this listing, leaving this heavily traded species vulnerable to further overexploitation (6).
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Description

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The porbeagle is a stout, heavy shark with a pointed, conical snout and a crescent-shaped caudal, or tail, fin. Its name is thought to arise from a combination of 'porpoise' referring to its shape, and 'beagle' referring to its hunting ability (3). It is dark bluish-grey to bluish-black on top, and white underneath (4). The first dorsal fin is large and triangular and has a white patch on the back of it, whilst the second dorsal fin is very small. The large pectoral fins, used for balancing and breaking, are situated behind long gill slits (2) (4). The porbeagle, which has moderately large blade-like teeth (2), is related to the much-feared shortfin mako and white shark, but seldom, if ever, attacks humans (3).
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Habitat

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The porbeagle generally inhabits waters over continental shelves, but is also found far from land in ocean basins and occasionally close inshore, at depths less than one meter down to at least 700 metres. It prefers waters colder than 18°C but greater than 1°C (2).
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Range

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The porbeagle occurs in the Atlantic Ocean in the northern hemisphere, and has a circumglobal distribution in the southern hemisphere; through the southern Atlantic, southern Indian Ocean, southern Pacific and Antarctic Ocean (2) (3).
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Status

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Classified as Vulnerable (VU) on the IUCN Red List (1). The Northeast Atlantic and Mediterranean subpopulations are classified as Critically Endangered (CR) and the Northwest Atlantic subpopulation is classified as Endangered (EN) on the IUCN Red List (1).
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Threats

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The greatest threat to porbeagles comes from the fisheries industry. It has been targeted by commercial fisheries in the North Atlantic and Mediterranean and is frequently caught as by-catch in the southern hemisphere. The porbeagle is utilised for human consumption, for oil and fishmeal and for fins for sharkfin soup (2). This exploitation has had a significant impact on porbeagle populations; the porbeagle has virtually disappeared from Mediterranean records (1), and abundance of the northwest Atlantic population in 2004 was at a record low (5). It is estimated that the northwest Atlantic population may take a minimum of several decades to recover from its current low abundance (5). At present there is no evidence to indicate that the decline in porbeagle abundance has ceased (5), and yet regulated Norwegian, Canadian and New Zealand fisheries for porbeagles still continue (2).
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Brief Summary

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The porbeagle, also known as the mackerel shark, is a heavy-built shark with a distinctly pointed snout. Some people refer to them as 'nose sharks'. Porbeagles eat all kinds of fish, from herring and mackerel to benthic fish. Every once in a while, they'll even take a bite of a scuba diver.
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Benefits

provided by FAO species catalogs
This species has been heavily fished commercially and utilized for human consumption in the temperate North Atlantic and the Mediterranean, but is also caught as bycatch in the Southern Hemisphere where it is the second most common shark as bycatch of the New Zealand longline fishery. World catches of porbeagles have been reported to FAO by a number of countries, including Canada, Denmark, the Channel and Faeroe Islands, France, Germany, Iceland, Malta, New Zealand, Norway, Portugal, Spain, Saint Pierre and Miquelon Islands, Sweden, the United Kingdom, and the United States. World catches per annum ranged from 346 to 9 674 t from 1951 through 1997 (mean 2 102 t) with 1 736 t reported in 1997 (FAO FishStat Plus database, 2000). The major peak was in the middle 1960s and was followed by a declining trend with peaks and declines in the 1970s and 1980s to a level between 1 000 and 2 500 t in the 1990s. Stocks in the North Atlantic have shown signs of serious overfishing in the form of greatly declining catches. Scandinavian fishers have caught porbeagles since the early nineteenth century, but only intensively during the twentieth century. Norway and to a lesser extent Denmark have been the principle fishers of porbeagles in the North Atlantic. Norwegian catches have varied wildly during the twentieth century, increasing from 279 t in 1926 to 3 884 t in 1933, then declining steadily to low levels during the second world war. Intensive fishing resumed in 1945 and peaked at 2 824 t in 1947, but then steadily declined to 207 t in 1970 and only 25 t in 1994. Porbeagles became scarce off Europe and the Norwegian fishery spread to the western North Atlantic, but eventually the fishery shifted to other species such as shortfin mako and swordfish. Small regulated catches exist at present for Norway (200 t allocated in European Community waters per year) and New Zealand, with the species protected in United States waters and regulated in the European Community. Canadian catches of porbeagles were less than 100 t/y until 1990 but landings increased in 1992 and catches have oscillated around 1 300 t/y since 1994. The western Atlantic stock is currently considered overexploited, with declining catch rates, and a fishing mortality beyond the replacement level. A Canadian management plan that limits the number of licenses, types of gear, fishing areas and seasons, prohibits finning, and restricts recreational fishing to catch-and-release only, has been in force since 1995. A TAC of 1 000 t/y was introduced in the commercial fishery for the period 1997-1999 pending better scientific information about resource status. In the past porbeagles were considered a nuisance to commercial fishermen because they wrecked light gear set for bony fishes (such as cod nets) and bit fish off hooks, but probably not so much at present with greatly depleted porbeagle stocks and decimated stocks of some of its prey species (including cod). A considerable bycatch fishery for porbeagle by Japanese longliners and probably the pelagic fishing fleets of other countries has existed in the southern Indian Ocean and probably elsewhere in the Southern Hemisphere. The catch is poorly known and may be little-utilized except for fins. It has figured as complementary bycatch (fins utilized) of the Japanese longline fishery for southern bluefin tuna off Tasmania. It is used fresh and dried-salted for human consumption; for oil and fishmeal for fertilizer; and for fins for shark-fin soup.The species is primarily caught with pelagic longlines; also pelagic trawl and bottom trawl, handlines and gill nets. It has recently showed up as bycatch of demersal longlines for Patagonian toothfish (Dissostichus eleginoides, Nototheniidae) in the southern Indian Ocean. Statistics for the Southern Hemisphere porbeagle fishery are only reported to FAO by New Zealand (21 t in 1997), which suggests that the southern catch is largely unreported. This species has been described as a relatively less active game fish compared to the shortfin mako and white shark. However, the porbeagle has been regularly sought by sportsfishing anglers in the United Kingdom, Ireland and the United States and is a strong fighter (especially on light tackle from a small boat). It is listed as a record game fish by the International Game Fish Association. Conservation Status : The conservation status of the porbeagle is of major concern because of the drastic decline in catches from targeted fisheries in the North Atlantic and continuing exposure of the species to intensive high-seas pelagic longline fisheries (with finning and capture trauma contributing to mortality) wherever it occurs. North Atlantic fisheries are relatively well-documented and under regulation, but not those of the Southern Hemisphere with the exception of New Zealand. Additional information from IUCN database Additional information from CITESdatabase
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Sharks of the world. An annotated and illustrated catalogue of shark species known to date. Volume 2 Bullhead, mackerel and carpet sharks (Heterodontiformes, Lamniformes and Orectolobiformes).Leonard J.V. Compagno 2001. FAO Species Catalogue for Fishery Purposes. No. 1, Vol. 2. Rome, FAO. 2001. p.269.
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Brief Summary

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A common littoral and epipelagic shark, most abundant on the continental offshore fishing banks but also found far from land in ocean basins and occasionally close inshore. It was recently caught at the mouth of a brackish estuary in Argentina but does not penetrate fresh water.This shark usually occurs in cold water, less than 18° and down to 1°C, but was once recorded in water 23°C. It does not occur in equatorial seas as far as is known. The porbeagle is described as active and strong-swimming in pursuit of prey, but when hooked is relatively sluggish and inactive in comparison to the shortfin mako (Isurus oxyrinchus ), and does not engage in spectacular leaps like that species. The porbeagle is found at the surface down to the bottom, singly and in schools and feeding aggregations, and has been caught at depths down to at least 366 m. Porbeagles may come inshore and to the surface in summer, but will winter offshore and beneath the surface. Fisheries catches in Europe indicate that the porbeagle has populational segregation by size (age) and sex. Porbeagles of the western North Atlantic seem to constitute a single stock that undertakes extensive migrations between southern Newfoundland (Canada) in summer to at least Massachusetts (USA) in the winter. Longterm tagging data suggest there is no mixing between this population and that of the eastern North Atlantic. Porbeagles breed on both sides of the North Atlantic, off the Atlantic coast of Europe and the British Isles, where females have embryos during most of the year except July through September, and off North America from Massachusetts to Maine, where females can be found with young at all times of year. Young are apparently born in the spring off Europe, in either winter-spring or late summer off North America, and probably from April to September (peak June-July [winter]) in the Southern Hemisphere. Mating in European waters occurs in late summer, and breeding there probably occurs every year. An extended mating period seems to exist for Southern Hemisphere populations around Australia and New Zealand. The porbeagle is ovoviviparous and a uterine cannibal (oophagous), with litters of 1 to 5 young but the majority of litters are of four young. The foetuses grow enormously by feeding on fertilized eggs, and develop grotesquely expanded abdomens and branchial regions. Small porbeagle embryos posses fang-like functional teeth to tear open egg capsules and release the contained ova; the fangs are shed at 34 to 38 cm FL (Francis and Stevens, 2000). The gestation period has been estimated at about 8 or 9 months for North Atlantic and South Pacific populations. The length of the entire reproductive cycle is not known. Pupping and nursery areas may be in continental waters, but are little-documented. In the western North Atlantic, mating is believed to take place off southern Newfoundland. Tag-recapture data and tetracycline injected sharks at liberty have been used to validate age determinations for porbeagles in the western North Atlantic up to age 10, but longevity could be as much as 30 to 45 years (Natanson, Mello and Campana, in press). Preliminary studies in this region suggest that males mature at about 175 cm FL ( Age 7) and females at around 212 cm FL ( Age 14) (Campana et al. 1999). Newborn porbeagles grow an estimated 15 to 20 cm per year (FL) during the first three years of life in the South Pacific. Prior to the intensive fishery that greatly reduced the numbers of this shark in European waters, the annual mortality for the species was an estimated 18% under low human exploitation and probably minimal predation pressure from other species. Recent research in Atlantic Canada indicates that the instantaneous natural mortality rate of porbeagles is about 0.1. This shark is a proverbially voracious feeder on small to moderate-sized pelagic schooling fishes, including mackerel (Scomber, Scombridae), pilchards and herring (Clupeidae), various gadoids such as cod, haddock, cusk, whiting (Gadidae) and hake (Merluccidae), icefishes (Channichthyidae) and John dories (Zeidae). Chondrichthyan prey include dogfish (Squalus acanthias, Squalidae) and tope sharks Galeorhinus galeus (Triakidae). Cephalopod prey includes squid and cuttlefish. It will scavenge hooked fishes including cod from longlines. Predators of the porbeagle are little known (apart from humans). A small specimen from Argentina had tooth marks suggestive of a carcharhinid, perhaps Carcharhinus brachyurus, but it is uncertain if these were from a predation bout or agonistic encounter. The white shark and orca are obvious candidates for porbeagle predators, but records of predation by either on porbeagles are not known to the author.
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Sharks of the world. An annotated and illustrated catalogue of shark species known to date. Volume 2 Bullhead, mackerel and carpet sharks (Heterodontiformes, Lamniformes and Orectolobiformes).Leonard J.V. Compagno 2001. FAO Species Catalogue for Fishery Purposes. No. 1, Vol. 2. Rome, FAO. 2001. p.269.
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Size

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Maximum total length 300+ cm, possibly to 370 cm but most smaller; size at birth between 60 and 75 cm TL (69 to 80 cm TL in South Pacific); males maturing at about 150 to 200 cm TL (196 cm TL in the western North Atlantic) and reaching at least 262 cm; females maturing at about 200 to 250 cm TL (with one reported at only 152 cm), to possibly 370 cm (with most less than 300 cm). Females mature at about 237 cm TL in the western North Atlantic and at about 185 to 202 cm TL in the South Pacific. There are several morphometric and L-W equations for porbeagles: Kohler, Casey and Turner (1995): W(kg) = 1.4823 x 10-5 x FL(cm)2.9641 (n = 15, western North Atlantic) where: FL(cm) = 1.7939 + 0.8971 x TL(cm) (n = 13) Campana et al. (1999): W(kg) = 0.5 x 10-4 x FL(cm)2.713 (n = 286, western North Atlantic) where: FL(cm) = 0.99 + 0.885 x TL(cm) (n = 361) Campana et al. (1999): FL(cm) = 4.96 x IDL(cm)0.901 (n = 358) Campana et al. (1999): FL(cm) = 1.7 + 1.12 PCL(cm) (n = 360) Francis and Stevens (2000): PCL(cm) = -1.366 + 0.907 FL(cm) (n = 866, FL = 61 to 223 cm, New Zealand) Francis and Stevens (2000): TL(cm) = 4.165 + 1.098 FL(cm) (n = 173, FL = 63 to 180 cm, Australia)
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Sharks of the world. An annotated and illustrated catalogue of shark species known to date. Volume 2 Bullhead, mackerel and carpet sharks (Heterodontiformes, Lamniformes and Orectolobiformes).Leonard J.V. Compagno 2001. FAO Species Catalogue for Fishery Purposes. No. 1, Vol. 2. Rome, FAO. 2001. p.269.
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Diagnostic Description

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fieldmarks: Heavy spindle-shaped body, moderately long conical snout, moderately large blade-like teeth with lateral cusplets, long gill slits, large first dorsal fin with abruptly white free rear tip, minute, pivoting second dorsal and anal fins, strong keels on caudal peduncle, short secondary keels on caudal base, crescentic caudal fin, ventral surface of body white and not extending over pectoral bases as white patches. Snout long and sharply pointed, with preoral length 5.9 to 9.0% of total length (adults 5.9 to 7.3%) and space from eye to first gill slit 1.7 to 2.5 times preorbital length. First upper lateral teeth with nearly straight cusps. Total vertebral count 150 to 162, precaudal vertebral count 85 to 91. Cranial rostrum with enlarged but discrete hypercalcified rostral cartilages, not forming a massive knob. Colour: grey or bluish grey to blackish above, white below, with white abdominal colour terminating at rear end of pectoral bases; first dorsal fin with an abruptly white or greyish white free rear tip; ventral surface of head white and abdomen without dusky blotches in adults of typical Northern Hemisphere porbeagles, but underside of head dark and abdomen blotched in some Southern Hemisphere adults.

References

  • Aasen, (1961, 1963)
  • Baldridge , (1974)
  • Campana et al. (1999)
  • Compagno , (19841990b, c;)
  • (No Author) , (1985)
  • Duhamel & Ozouf-Costaz , (1982)
  • Farquhar, 1963
  • Fowler, (1936, 1941)
  • Francis & Stevens, (2000)
  • Garman, (1913)
  • I. Fergusson, (pers. comm.)
  • Lahille, (1928)
  • Last & Stevens, (1994)
  • Lucifora & Menni, (1997)
  • Nakaya, 1971
  • Natanson, Mello & Campana, (in press)
  • O'Boyle et al. (1998)
  • Paust and Smith, 1986
  • (No Author) , (1984)
  • Sadowsky & Amorim, (1977)
  • Santos, Porteiro & Barreiros, (1997)
  • Schwartz & Burgess, (1975)
  • Shann, (1911, 1923)
  • Smith, (1949)
  • Stevens, (1973)
  • Stevens, (1990)
  • Stevens, Dunning & Machida, (1983)
  • Svetlov, (1978)
  • Templeman, (1963)
  • Whitley, (1939, 1940)

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Sharks of the world. An annotated and illustrated catalogue of shark species known to date. Volume 2 Bullhead, mackerel and carpet sharks (Heterodontiformes, Lamniformes and Orectolobiformes).Leonard J.V. Compagno 2001. FAO Species Catalogue for Fishery Purposes. No. 1, Vol. 2. Rome, FAO. 2001. p.269.
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Distribution

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Coastal and oceanic, amphitemperate.Coastal and oceanic, amphitemperate, with centres of distribution in the North Atlantic and in a circumglobal band of temperate water of the southern Atlantic, southern Indian Ocean, southern Pacific and Antarctic Ocean. Western Atlantic: Greenland, Canada (Newfoundland Banks, Gulf of St. Lawrence and Nova Scotia), United States (Maine, Massachusetts, Rhode Island, rarely New York, New Jersey and possibly South Carolina), and Bermuda; southern Brazil and Uruguay to southern Argentina. Eastern Atlantic: Iceland and western Barents Sea to Baltic and North Seas, English Channel, Straits of Gibraltar, and Mediterranean Sea, including Russia, Norway, Sweden, Denmark, Germany, Holland, Scotland, England, Wales, Ireland, the Orkney Islands, France, Portugal, Spain, and Gibraltar; entire coast of Mediterranean Sea but not in Black Sea; Morocco, Madeira, Azores, possibly the Gulf of Guinea, and off South Africa (Western Cape). Indo-West Pacific: South-central Indian Ocean from South Africa (Eastern Cape and possibly KwaZulu-Natal) eastward to between Prince Edward and Crozet Islands, between Kerguelen and St. Paul Islands, and the southern coast of Australia (southern Western Australia and South Australia, Victoria, Tasmania, New South Wales and southern Queensland), New Zealand (including Stewart Island). Subantarctic waters off South Georgia, Marion, Prince and Kerguelen Islands. Eastern South Pacific: southern Chile south to Cape Horn.
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Sharks of the world. An annotated and illustrated catalogue of shark species known to date. Volume 2 Bullhead, mackerel and carpet sharks (Heterodontiformes, Lamniformes and Orectolobiformes).Leonard J.V. Compagno 2001. FAO Species Catalogue for Fishery Purposes. No. 1, Vol. 2. Rome, FAO. 2001. p.269.
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Diagnostic Description

provided by Fishbase
A stout, spindle-shaped shark with large black eyes, a sharp, conical snout, long gill slits, and small, smooth-edged, narrow teeth with side cusps (Ref. 5578, 88171). Strong keels on the caudal peduncle, short secondary keels on the caudal base, and a crescentic caudal fin; the insertion of the small second dorsal fin is above the insertion of the anal fin (Ref. 88171). Dark grey dorsally, white ventrally, without blotches (Ref. 6581, 43278); rear tip of 1st dorsal abruptly white (Ref. 5578).
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Recorder
Cristina V. Garilao
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Life Cycle

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Distinct pairing with embrace (Ref. 205). Ovoviviparous (aplacental viviparity), with uterine cannibalism (embryos feeding on other ova produced by the mother (oophagy) after the yolk sac is absorbed) (Ref. 43278, 50449). With 1-5 (usually 4) pups in a litter (Ref. 6871, 43278). Reproduction probably yearly (Ref. 45602). In the northeast Atlantic, breeding grounds are off the coast of Europe and the British Isles. Embryos found in mature females throughout the year except from July to September. Mating occurs in late summer, pups are born in the spring of the following year (Ref. 43278). Gestation may last 8-9 months. Size at birth 60-80 cm TL (Ref. 6871, 43278).
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Armi G. Torres
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Migration

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Oceanodromous. Migrating within oceans typically between spawning and different feeding areas, as tunas do. Migrations should be cyclical and predictable and cover more than 100 km.
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Kent E. Carpenter
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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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Occurs on the continental shelf (Ref. 75154).
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Pascualita Sa-a
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Biology

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Occurs inshore to offshore fishing banks and occasionally to open ocean areas. It is migratory, moves generally along the continental shelves (inshore to surface during simmer) and winters offshore in deeper water (Ref. 58085). Most abundant on continental offshore fishing banks but also found far from land in ocean basins and occasionally close inshore (Ref. 247). Extreme depth reported to 1,360 meters. Age attained in North Atlantic at least 26 years and in the Southern Hemisphere probably 65 years (Ref. 119696). Specimens tagged off southern England were recaptured in northern Norway (having travelled 2,370 km), Denmark and Spain (Ref. 88752, 88753). The northwest Atlantic stock migrates from Newfoundland, Canada in the winter to Massachusetts in the summer (Ref. 43278, 88754). Trans-Atlantic migrations have also been recorded. One of the most cold-tolerant sharks; in the northwest Atlantic mostly found from 5-10°C (Ref. 88755); with extremes of -1°C and 23°C (Ref. 119696). Known to temporarily tolerate salinities as low as 10 to follow its prey (Ref. 88740). Found singly and in schools and feeding aggregations (Ref. 247). Feeds on small and medium-sized pelagic schooling species, other sharks, squid (Ref. 5578) and demersal fishes (cod, white hake, red hake, haddock and cusk (Ref. 5951, 43278)). Ovoviviparous species (Ref. 43278, 50449). Females grow larger than males (Ref. 88756). Parasites include Phyllobothrium dagnallium (found in stomach, intestine and spiral valve) and Dinobothrium sp. (Ref. 5951). Regarded as potentially dangerous to people because of its size and activity but has never or very seldom been indicted in an attack on people or boats (Ref. 247). Considered by some as a sport fish (Ref. 84357). The flesh of the porbeagle is of good quality and texture and is said to taste like swordfish (Ref. 84357). Utilized fresh, dried or salted and frozen for human consumption; for oil and fishmeal; fins for shark-fin soup (Ref. 247). May be pan-fried and broiled (Ref. 9988). Catch records and studies in the northeast Atlantic show segregation by sex and size (Ref. 56108, 88756, 88757).
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Importance

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fisheries: commercial; gamefish: yes
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Porbeagle

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The porbeagle or porbeagle shark (Lamna nasus) is a species of mackerel shark in the family Lamnidae, distributed widely in the cold and temperate marine waters of the North Atlantic and Southern Hemisphere. In the North Pacific, its ecological equivalent is the closely related salmon shark (L. ditropis). It typically reaches 2.5 m (8.2 ft) in length and a weight of 135 kg (298 lb); North Atlantic sharks grow larger than Southern Hemisphere sharks and differ in coloration and aspects of life history. Gray above and white below, the porbeagle has a very stout midsection that tapers towards the long, pointed snout and the narrow base of the tail. It has large pectoral and first dorsal fins, tiny pelvic, second dorsal, and anal fins, and a crescent-shaped caudal fin. The most distinctive features of this species are its three-cusped teeth, the white blotch at the aft base of its first dorsal fin, and the two pairs of lateral keels on its tail.

The porbeagle is an opportunistic hunter that preys mainly on bony fishes and cephalopods throughout the water column, including the bottom. Most commonly found over food-rich banks on the outer continental shelf, it makes occasional forays both close to shore and into the open ocean to a depth of 1,360 m (4,460 ft). It also conducts long-distance seasonal migrations, generally shifting between shallower and deeper water. The porbeagle is fast and highly active, with physiological adaptations that enable it to maintain a higher body temperature than the surrounding water. It can be solitary or gregarious, and has been known to perform seemingly playful behavior. This shark is aplacental viviparous with oophagy, developing embryos being retained within the mother's uterus and subsisting on non-viable eggs. Females typically bear four pups every year.

Only a few shark attacks of uncertain provenance have been attributed to the porbeagle. It is well regarded as a game fish by recreational anglers. The meat and fins of the porbeagle are highly valued, which has led to a long history of intense human exploitation. However, this species cannot sustain heavy fishing pressure due to its low reproductive capacity. Direct commercial fishing for the porbeagle, principally by Norwegian longliners, led to stock collapses in the eastern North Atlantic in the 1950s, and the western North Atlantic in the 1960s. The porbeagle continues to be caught throughout its range, both intentionally and as bycatch, with varying degrees of monitoring and management. The International Union for Conservation of Nature (IUCN) has assessed the porbeagle as vulnerable worldwide, and as either endangered or critically endangered in different parts of its northern range.

Taxonomy

A calcareous skeletal structure that looks like a thick tripod
The calcified rostral (snout) cartilages of a porbeagle: Its specific epithet nasus means "nose".

The etymology of the word "porbeagle" is obscure. A common suggestion is that it combines "porpoise" and "beagle", referencing this shark's shape and tenacious hunting habits.[3] Another is that it is derived from the Cornish porth, meaning "harbor", and bugel, meaning "shepherd".[4] The Oxford English Dictionary states that the word was either borrowed from Cornish or formed from a Cornish first element with the English "beagle". The Dictionary also notes that no evidence exists for a connection to the French porc, meaning "swine", or to porpoise, as has been proposed.[5] Other common names for the porbeagle include Atlantic mackerel shark, Beaumaris shark, bottle-nosed shark, and blue dog.[3]

The first scientific description of the porbeagle was authored by French naturalist Pierre Joseph Bonnaterre in the 1788 Tableau encyclopédique et methodique des trois règnes de la nature, and based on an earlier 1769 account by Welsh naturalist Thomas Pennant. Bonnaterre named the shark Squalus nasus, the specific epithet nasus being Latin for "nose".[3][6] In 1816, French naturalist Georges Cuvier placed the porbeagle into its own subgenus, Lamna, which later authors elevated to the rank of full genus.[7]

Phylogeny and evolution

Several phylogenetic studies, based on morphological characters and mitochondrial DNA sequences, have established the sister species relationship between the porbeagle and the salmon shark (L. ditropis),[8][9] which occurs in place of it in the North Pacific.[10] The genus Lamna evolved 65–45 Mya. When its two extant species diverged from each other is uncertain, though the precipitating event was likely the formation of the ice cap over the Arctic Ocean, which would have isolated sharks in the North Pacific from those in the North Atlantic.[11][12]

Fossilized porbeagle remains are known from Late Miocene epoch (about 7.2 Mya) deposits in Belgium and the Netherlands, Pliocene epoch (5.3–2.6 Mya) deposits in Belgium, Spain, and Chile, and Pleistocene epoch (2.6 Mya to 12,000 BP) deposits in the Netherlands.[13][14][15] However, Lamna teeth that closely resemble those of the porbeagle have been found in the La Meseta Formation on Seymour Island off the Antarctic Peninsula, which date to the middle to late Eocene epoch (50–34 Mya). Much taxonomic confusion remains regarding Lamna in the fossil record due to the high degree of variability in adult tooth morphology within species.[14][16]

Distribution and habitat

The porbeagle has an almost global amphitemperate distribution, i.e. it is absent from the tropics; in the North Pacific, its niche is assumed by the salmon shark. It is found mostly within 30–70°N and 30–50°S latitudes.[10] In the North Atlantic, the northern limit of its range extends from the Newfoundland Grand Banks off Canada, through southern Greenland, to Scandinavia and Russia; the southern limit of its range extends from New Jersey and Bermuda, through the Azores and Madeira, to Morocco. It is found in the Mediterranean Sea, but not the Black Sea. Normally, North Atlantic sharks only stray as far south as South Carolina and the Gulf of Guinea,[7] but pregnant females from the western North Atlantic population are known to range into the Sargasso Sea, almost as far as Hispaniola, to give birth.[17] In the Southern Hemisphere, the porbeagle apparently occupies a continuous band bound in the south by the Antarctic Convergence, and extending as far north as Chile and Brazil, the Western Cape province of South Africa, Australia to southern Western Australia and southern Queensland, and New Zealand.[7] In New Zealand it is most common south of the Cook Strait.[18] The porbeagle is thought to have colonized the Southern Hemisphere during the Quaternary glaciation (beginning around 2.6 Mya), when the tropical climate zone was much narrower than it is today.[12]

Offshore fishing banks are the favored habitat of the porbeagle, though it can be found from a depth of 1,360 m (4,460 ft) in oceanic basins to littoral (close to shore) waters less than 1 m (3.3 ft) deep, over the entire water column.[7][19][20] A single, anomalous record was made of a juvenile in brackish water in Mar Chiquita in Argentina.[21] A tracking study off the British Isles has found substantial variation in the short-term movements of this species, both between and within individuals. Vertical movements tended to increase with water depth and corresponding temperature stratification; in shallow, unstratified waters, sharks either showed no pattern in changing depth or made reverse diel movements, spending the day in shallow water and descending at night. In deeper, stratified waters, the sharks performed a regular diel migration, spending the day below the thermocline and rising towards the surface at night.[22] The porbeagle has been reported across a temperature range of 1 to 23 °C (34 to 73 °F), with most records between 8 and 20 °C (46 and 68 °F).[7][23] In a study that included 420 porbeagles caught in the northwest Atlantic off Canada, all were in water below 13 °C (55 °F) and the majority between 5 and 10 °C (41 and 50 °F).[23]

Porbeagle populations in the Northern and Southern Hemispheres appear to be completely separate. Two stocks are in the North Atlantic, east and west, that seldom mix; only one individual is known to have crossed the Atlantic, covering 4,260 km (2,650 mi) from Ireland to Canada. Several discrete stocks are likely present in the Southern Hemisphere, as well. This species segregates by size and sex in the North Atlantic, and at least by size in the South Pacific. For example, males outnumber females 2:1 off Spain, females are 30% more numerous than males off Scotland, and immature males are predominant in the Bristol Channel. Older, larger sharks may frequent higher latitudes than younger individuals.[10]

Seasonal migrations have been observed in porbeagles from both hemispheres. In the western North Atlantic, much of the population spends the spring in the deep waters of the Nova Scotia continental shelf, and migrates north a distance of 500–1,000 km (310–620 mi) to spend late summer and fall in the shallow waters of the Newfoundland Grand Banks and the Gulf of St. Lawrence.[10][17][24] In December, large, mature females migrate south over 2,000 km (1,200 mi) into the Sargasso Sea for pupping, keeping deeper than 600 m (2,000 ft) during the day and 200 m (660 ft) at night so as to stay in the cooler waters beneath the Gulf Stream.[20] In the eastern North Atlantic, porbeagles are believed to spend spring and summer in shallow continental shelf waters, and disperse northwards to overwinter in deeper waters offshore.[22] Migrating sharks may travel upwards of 2,300 km (1,400 mi), though once they reach their destination they tend to remain within a relatively localized area.[10][20][22] In the South Pacific, the population shifts north past 30°S latitude into subtropical waters in winter and spring, and retreats south past 35°S latitude in summer, when sharks are frequently sighted off subantarctic islands.[10]

Description

Side view of a blue-gray shark
A Southern Hemisphere porbeagle showing the white patch on the rear tip of the first dorsal fin, which is unique to the species.

The porbeagle is a very stout-bodied shark with a fusiform (spindle-like) shape. The long, conical snout tapers to a sharp point, and is supported by enlarged, highly calcified rostral cartilages. The eyes are large and black, without nictitating membranes (protective third eyelids). The small, S-shaped nostrils are positioned in front of and below the level of the eyes. The mouth is large and strongly curved, with moderately protrusible jaws.[7] North Atlantic sharks have 28–29 upper tooth rows and 26–27 lower tooth rows, while Southern Hemisphere sharks have 30–31 upper tooth rows and 27–29 lower tooth rows.[25] Each tooth has a strongly arched base and a nearly straight, awl-like central cusp, which is flanked by a pair of smaller cusplets in all but the smallest individuals. The five pairs of gill slits are long and precede the pectoral fin bases.[7]

The pectoral fins are long and narrow. The first dorsal fin is large and high, with a rounded apex, and originating just behind the pectoral fin bases. The pelvic fins are much smaller than the first dorsal fin. The second dorsal and anal fins are smaller still, and placed about even with each other on narrow bases that allow pivoting from side to side. The sides of the caudal peduncle are expanded into prominent lateral keels. A second, shorter pair of keels are present below the main keels. The caudal fin is large and crescent-shaped, with the lower lobe almost as long as the upper; both dorsal and ventral depressions (precaudal pits) are at the caudal fin base, and a deep ventral notch is near the tip of the upper caudal fin lobe.[7] The skin is soft and covered by tiny, flattened dermal denticles (scales), lending a velvety texture. Each denticle has three horizontal ridges that lead to teeth on the posterior margin.[3]

The dorsal coloration is a medium to dark gray or slate, extending to the bases of the pectoral fins. The underside is white; adults in the Southern Hemisphere often have dark coloring under the head and dusky blotches scattered over the belly. The free rear tip of the first dorsal fin is abruptly light gray or white, a feature unique to this species. The porbeagle may attain a length of 3.7 m (12 ft), though this is uncertain and may have resulted from confusion with other mackerel shark species. A more typical length is 2.5 m (8.2 ft).[7][17][19] Female sharks grow larger than males in the North Atlantic, with maximum confirmed fork lengths (snout tip to caudal fin fork) of 2.5 m (8.2 ft) for males and 3.0 m (9.8 ft) for females. Southern Hemisphere sharks are smaller and the two sexes are similar in size, with males and females attaining fork lengths of 2.0 m (6.6 ft) and 2.1 m (6.9 ft) respectively.[10] Most porbeagles weigh no more than 135 kg (298 lb), with the record being a 230 kg (510 lb) individual caught off Caithness, Scotland, in 1993.[7][21]

Biology and ecology

View of the front half of a shark with large black eyes and open mouth showing many rows of sharp teeth, lying on a pier
The streamlined shape and long gill slits of the porbeagle are adaptations for a fast, active lifestyle.

Fast and energetic, the porbeagle can be found singly or in groups.[7] Its fusiform body, narrow caudal peduncle with lateral keels, and crescent-shaped tail are adaptations for efficiently sustaining speed, which have also been independently evolved by tunas, billfishes, and several other groups of active fishes. The salmon shark and it are the thickest-bodied members of their family (length-depth ratio approaching 4.5), and consequently have the stiffest swimming style; they oscillate their tails while holding their bodies mostly rigid, which confers propulsive power with high energy efficiency, but at the cost of maneuverability. The large gill surface area of the porbeagle allows more oxygen to be delivered to its tissues. It also has a short band of aerobic "red muscle" along each side, which can contract independently of the regular "white muscle" at a lower energy cost, enhancing the shark's stamina.[26][27]

Porbeagles are among the few fishes that exhibit apparent play behavior.[21] Reports, principally off the Cornish coast, have this species rolling and repeatedly wrapping themselves in long kelp fronds near the surface; this activity may have an exploratory or self-stimulatory purpose, though alternately, the sharks may be attempting to feed on small kelp organisms or scrape off parasites.[21][28] In addition, porbeagles within a group have been seen chasing each other, and they will reportedly "play with anything floating on the water"; individuals have been observed prodding, tossing, or biting natural and artificial objects, including pieces of driftwood and balloon floats used by anglers.[21][28][29]

Great white sharks (Carcharodon carcharias) and killer whales (Orcinus orca) are plausible, albeit undocumented, predators of the porbeagle. In one record, a small individual caught off Argentina bore bite marks from a copper shark (Carcharhinus brachyurus) or similar species, but whether the porbeagle was the target of attempted predation or if the two were simply involved in interspecific aggression is uncertain.[7] Known parasites of this species include the tapeworms Dinobothrium septaria and Hepatoxylon trichiuri,[30][31] and the copepods Dinemoura producta,[32] Laminifera doello-juradoi,[33] and Pandarus floridanus.[34] Natural annual mortality is low, estimated to be 10% for juveniles, 15% for adult males, and 20% for adult females in the western North Atlantic.[10]

Feeding

Two arrowhead-shaped shark teeth
Porbeagle teeth are suited for grasping fish, with a long central cusp and a tiny cusplet on either side.

The porbeagle is an active predator that predominantly ingests small to medium-sized bony fishes. It chases down pelagic fishes such as lancet fish, mackerel, pilchards, herring, and sauries, and forages near the bottom for groundfishes such as cusk, haddock, redfish (i.e., Sebastes, Lutjanus, Trachichthyidae, and Berycidae),[35] cod, hake, icefish, dories, sand lances, lumpsuckers, and flatfish. Cephalopods, particularly squid, also form an important component of its diet, while smaller sharks such as spiny dogfish (Squalus acanthias) and tope sharks (Galeorhinus galeus) are rarely taken. Examinations of porbeagle stomach contents have also found small shelled molluscs, crustaceans, echinoderms, and other invertebrates, which were likely ingested incidentally, as well as inedible debris such as small stones, feathers, and garbage fragments.[3][21][24]

In the western North Atlantic, porbeagles feed mainly on pelagic fishes and squid in spring, and on groundfishes in the fall; this pattern corresponds to the spring-fall migration of these sharks from deeper to shallower waters, and the most available prey types in those respective habitats. Therefore, the porbeagle seems to be an opportunistic predator without strong diet specificity.[24] During spring and summer in the Celtic Sea and on the outer Nova Scotian Shelf, porbeagles congregate at tidally induced thermal fronts to feed on fish that have been drawn by high concentrations of zooplankton.[22][23] Hunting porbeagles regularly dive from the surface all the way to the bottom, cycling back every few hours; this vertical movement may aid in the detection of olfactory cues.[22] A one-year-old porbeagle 1 m (3.3 ft) long, was reported to have had fed on krill and polychaete worms.[32]

Life history

The dissected reproductive system of an adult male shark; the paired testes are connected by the tubular epididymis to the base of a pair of cylindrical claspers. Inset close-ups show the base, or head, of the epididymis, and the ampulla, which comprises the lower section of the epididymis. Another label indicates the epigonal organ, located near the lower end of the testes
The dissected reproductive system of an adult female shark: there is a single large, round ovary, which leads into a junction that splits off into the lower uterus, which leads to the vagina and then the cloaca, and a pair of anterior uteri, each connected to an oviducal gland by a narrow tract or isthmus
The male (top) and female (bottom) reproductive systems of the porbeagle (click to enlarge).

The timing of the porbeagle's reproductive cycle is unusual in that it is largely similar in both hemispheres, rather than being offset by six months. This suggests that its reproduction is not significantly affected by temperature or day length, perhaps owing to its endothermic physiology.[36] Mating takes place mainly between September and November, though females with fresh mating scars have been reported as late as January off the Shetland Islands. The male bites at the female's pectoral fins, gill region, and flanks while courting and to hold on for copulation.[37] Two mating grounds are known for western North Atlantic porbeagles, one off Newfoundland and the other on Georges Bank in the Gulf of Maine.[37][38] Adult females have a single functional ovary, on the right, and two functional uteri. They probably reproduce every year. The litter size is typically four, with two embryos oriented in opposing directions sharing each uterus; on rare occasions, a litter may contain as few as one or as many as five pups.[36] The gestation period is 8–9 months.[7][37]

Like other members of its family, the porbeagle is aplacental viviparous with oophagy, i.e. the main source of embryonic nutrition are unfertilized eggs. During the first half of pregnancy, the mother ovulates enormous numbers of tiny ova, packed into capsules up to 7.5 cm (3.0 in) long, into her uteri. A newly conceived embryo is sustained by a yolk sac and emerges from its egg capsule at 3.2–4.2 cm (1.3–1.7 in) long. At this time, the embryo has well-developed external gills and a spiral valve intestine. When the embryo is 4.2–9.2 cm (1.7–3.6 in) long, it has resorbed its external gills and most of its yolk sac, but cannot yet feed, as it lacks the means to open egg capsules. At a length of 10–12 cm (3.9–4.7 in), the embryo grows two massive, recurved "fangs" in the lower jaw for tearing open capsules, as well as two much smaller teeth in the upper jaw. It begins to feed voraciously on yolk, acquiring an enormously distended stomach; to accommodate this, the muscles on the belly split down the middle and the skin on the abdomen stretches greatly.[36][37]

At 20–21 cm (7.9–8.3 in) long, the embryo appears pink because it lacks pigment except in its eyes, and its head and gill regions are laterally enlarged and gelatinous. The yolk stomach can comprise up to 81% of the embryo's total weight when it is 30–42 cm (12–17 in) long. The embryo gains pigment and sheds its fangs at a length of 34–38 cm (13–15 in). Around this time, the mother stops producing ova. From then on, the embryo relies mainly on the yolk stored in its stomach, though it may continue to feed on remaining eggs by squishing the capsules between its jaws or swallowing them whole. It begins to transfer its energy stores from its stomach to its liver, causing the former to shrink and the latter to grow exponentially. The embryo is essentially fully pigmented by a length of 40 cm (16 in), and has assumed its newborn appearance by a length of 58 cm (23 in). By then, its stomach has shrunk enough for the abdominal muscles to close, leaving what has been termed an "umbilical scar" or "yolk sac scar" (neither is accurate). Several series of single-cusped teeth grow in both jaws, though they lie flat and remain nonfunctional until birth.[36][37]

Two sharks lying on a boat deck, the one in front about half the size of the one in back, but otherwise similar in appearance
A juvenile porbeagle alongside an adult

Newborn porbeagles measure 58–67 cm (23–26 in) long and do not exceed 5 kg (11 lb). Up to a tenth of the weight is made up of the liver, though some yolk also remains in its stomach and continues to sustain the pup until it learns to feed.[10][36] The overall embryonic growth rate is 7–8 cm (2.8–3.1 in) per month.[36][37] Sometimes, one pup in a uterus is much smaller than the other, but otherwise normal. These "runts" may result from a dominant, forward-facing embryo eating most of the eggs as they arrive, and/or the mother being unable to provide an adequate egg supply for all her offspring.[36] Birthing occurs from April to September, peaking in April and May (spring-summer) for North Atlantic sharks and June and July (winter) for Southern Hemisphere sharks. In the western North Atlantic, birth occurs well offshore in the Sargasso Sea at depths around 500 m (1,600 ft).[20]

Both sexes grow at similar rates until the onset of maturation, with females maturing later and at a larger size than males.[39] In the first four years of life, the annual growth rate is 16–20 cm (6.3–7.9 in) and similar in both hemispheres; thereafter, sharks from the western South Pacific begin to grow slower than those from the North Atlantic.[40] In the North Atlantic, males mature at a fork length of 1.6–1.8 m (5.2–5.9 ft) and an age of 6–11 years, and females at a fork length of 2.0–2.2 m (6.6–7.2 ft) and an age of 12–18 years.[37][39] In the Southwest Pacific, males mature at a fork length of 1.4–1.5 m (4.6–4.9 ft) and an age of 8–11 years, and females at a fork length of 1.7–1.8 m (5.6–5.9 ft) and an age of 15–18 years.[36][40][41] The oldest porbeagle on record was 26 years of age and measured 2.5 m (8.2 ft) long.[42] The maximum lifespan of this species appears to be 30–40 years in the Atlantic,[42] but could be as much as 65 years in the South Pacific.[40]

Thermoregulation

A shark lying belly up and sliced transversely through the middle, showing the body cavity and the spinal column beneath it, surrounded by pink muscle with two obviously darker muscle blocks flanking the spine
Cross-section through the trunk of a porbeagle (orientation is belly-up); note the central red muscles.

Like other members of its family, the porbeagle is endothermic; metabolic heat generated by its red muscles is conserved within the body by specialized systems of blood vessels called retia mirabilia (Latin for "wonderful nets"; singular rete mirabile), that act as highly efficient countercurrent heat exchangers. The porbeagle has several rete mirabile systems: the orbital retia accessing its brain and eyes, the lateral cutaneous retia accessing its swimming muscles, the suprahepatic rete accessing its viscera, and the kidney rete.[27]

Among sharks, the porbeagle's capacity for elevating body temperature is second only to the salmon shark's. Its red muscles are located deep within the body, adjacent to the spine, and its lateral rete is composed of over 4,000 small arteries arranged in bands.[43] It has one of the highest core temperatures within its family, 8–10 °C (14–18 °F) warmer than that of the surrounding water.[44] Being warm-bodied may allow this shark to maintain higher cruising speeds, hunt in deep water for extended periods of time, and/or enter higher latitudes during winter to exploit food resources not available to other sharks.[27][32] The orbital retia of the porbeagle can raise the temperature of its brain and eyes by 3–6 °C (5–11 °F), and likely serve to buffer those sensitive organs against the large temperature shifts that accompany changes in depth; potential benefits of this include increased visual acuity and reduced response times.[45]

Human interactions

The porbeagle has very rarely, if ever, bitten swimmers or boats.[7] As of 2009, the International Shark Attack File attributes three bites to this species, one provoked and none fatal, and two on boats.[46] One older anecdote tells of a fisherman who provoked a porbeagle into leaping from the water and tearing his clothes. In another account of a swimmer bitten by a "mackerel shark", the species responsible could easily have been a misidentified shortfin mako or great white shark. Recently in the North Sea, adult porbeagles have been filmed charging at divers working on oil platforms, sometimes even brushing lightly against them without doing harm. These rushes do not appear to have predatory intent and may instead be motivated by curiosity or defense.[7]

On 14 May 2018, a porbeagle shark was reported to have bitten a fisherman off the coast of Cornwall, United Kingdom, as it was being returned to the sea.[1]

At one time, porbeagles were regarded as nuisances by some commercial fishers because they damaged lighter fishing gear intended for smaller species and took hooked fish from lines.[7] This shark is highly valued as a game fish by sport fishers in Ireland, the United Kingdom, and the United States. It fights strongly on hook-and-line, but does not usually jump into the air like the related shortfin mako shark. Novice anglers often mistake this shark for the mako, which has earned it the affectionate moniker "fako" in New England.[21] The International Game Fish Association keeps records on the porbeagle.[7][21]

Commercial fishing

Shark breaking the water surface next to a ship, with a fishing line coming from its mouth
A porbeagle is hooked on a longline; this shark is valued by both commercial and recreational fishers.

Prized for its meat and fins, the porbeagle has long been under heavy fishing pressure.[1] The meat is sold fresh, frozen, or dried and salted, and ranks among the most valuable of any shark: in 1997 and 1998, it had a wholesale price of 5–7 eur/kg, four times that of the blue shark (Prionace glauca). Most of the demand comes from Europe, though the United States and Japan also import this species. The fins are shipped to East Asia for use in shark fin soup. The remainder of the shark may also be used for production of leather, liver oil, and fishmeal. International trade in the porbeagle appears to be significant, but remains unquantified, as shark products tend not to be reported to the species level, and many consist of a mix of various species.[47][48] This shark is caught most readily on longlines, but is also susceptible to gillnets, driftnets, trawls, and handlines. It is valuable enough to be generally retained when caught as bycatch; if storage space cannot be spared, it may be finned and the carcass discarded.[1]

Intensive fishing for the porbeagle dates back the 1930s, when Norway and to a lesser extent Denmark began operating longline vessels in the Northeast Atlantic. The Norwegian annual catch rose from 279 tons in 1926 to 3,884 tons in 1933, and peaked at around 6,000 tons in 1947, with the resumption of fishing after World War II. Soon after, the stock collapsed; Norwegian annual catches declined steadily to 1,200–1,900 tons from 1953 to 1960, 160–300 tons in the early 1970s, and 10–40 tons in the late 1980s to early 1990s. Similarly, Danish annual catches fell from 1,500 tons in the early 1950s to under 100 tons in the 1990s.[7][49] France and Spain began to target porbeagles in the Northeast Atlantic in the 1970s. French fishers operate mainly in the Celtic Sea and the Bay of Biscay, and saw a decline from an annual catch over 1,000 tons in 1979 to 300–400 tons in the late 1990s. Catches by Spanish fishers were highly variable, ranging from negligible to over 4,000 tons per year, which may reflect shifts of fishing effort into historically less-exploited waters.[1] Since 2011, all fishing for the porbeagle has been illegal in waters of the European Union, and EU-registered vessels are also prohibited from fishing for the species in international waters.[50] In 2012, similar restriction came into effect in Norway.[51]

As porbeagles had become scarce in the Northeast Atlantic, in the 1960s, the Norwegian fishing fleet moved west to the waters off New England and Newfoundland. A few years later, they were joined by longline vessels from the Faroe Islands. Norwegian annual catches rose from 1,900 tons in 1961 to over 9,000 tons in 1965;[17] the catch was largely exported to Italy, where porbeagle (smeriglio) is an extremely popular food fish.[21][52] Again, the stock collapsed, this time in only six years; by 1970, Norwegian catches had fallen under 1,000 tons per year, and Faroese catches observed a similar trend. With the population decimated, most fishers moved on or switched to other species. Porbeagle numbers gradually recovered in the ensuing 25 years, to about 30% of pre-exploitation levels. In 1995, Canada established an Exclusive Economic Zone and became the primary fisher of porbeagles in the region. Between 1994 and 1998, Canadian fishing vessels landed 1,000–2,000 tons per year, which depleted the population to 11–17% of pre-exploitation levels by 2000.[17] Strict regulations and greatly reduced fishing quotas introduced in 2000 have since begun to reverse the stock decline, though recovery of the stock is projected to take decades due to the low productivity of the species.[53] Some evidence shows that incidental artificial selection caused by heavy fishing has led to a compensatory growth response, i.e. faster growth and earlier maturation.[54]

In the Southern Hemisphere, commercial fishing for the porbeagle is mostly undocumented. Substantial numbers are caught incidentally by pelagic longline fisheries targeting more valuable species such as southern bluefin tuna (Thunnus maccoyii), swordfish (Xiphias gladius), and Patagonian toothfish (Dissostichus eleginoides), including vessels operated by Japan, Uruguay, Argentina, South Africa, and New Zealand. Porbeagle catches by the Uruguayan tuna pelagic longline fishery peaked in 1984 with 150 tons landed. Records of catch per unit effort for this fishery have shown a 90% decline in porbeagle landings from 1988 to 1998, though whether this reflects a real population decline or changing fishing habits is uncertain. New Zealand has reported annual catches of 150–300 tons, mostly of immature individuals, from 1998 to 2003.[1]

Conservation

Monochromatic drawings of two sharks, one labeled
Historical illustration of a basking shark and a porbeagle (under the obsolete name Lamna cornubica), both commercially important species

The rapid collapse of porbeagle stocks on both sides of the North Atlantic is often cited as archetypal of the "boom and bust" pattern of most shark fisheries. Factors including a small litter size, long maturation time, and the capture of multiple age classes all contribute to this shark's susceptibility to overfishing.[55] The International Union for Conservation of Nature has assessed the porbeagle globally as vulnerable,[1] endangered in the western North Atlantic (including the Baltic),[52][56] and critically endangered in the eastern North Atlantic[49] and Mediterranean Sea.[57]

The porbeagle is listed on Annex 1 (Highly Migratory Species) of the UN Convention on the Law of the Sea and on Annex 1 of the Conservation of Migratory Species (CMS; also known as the Bonn Convention) Migratory Shark Memorandum of Understanding. This species benefits from bans on shark finning instituted by several nations and supranational entities, including Canada, the United States, Brazil, Australia, the European Union, and the International Commission for the Conservation of Atlantic Tunas. Although the Animals Committee of the UN Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES) recommended additional conservation actions for the porbeagle, CITES rejected proposals to list the species in 2008 and again in 2010.[1] In March 2013, the porbeagle was listed on Appendix II of CITES, allowing for increased regulation in the international trade of this species.[58]

In March 2015, The National Marine Fisheries Service (NMFS) responded to a court order to compile information as to whether the shark will be listed as threatened or endangered under the Endangered Species Act.[59]

Southern Hemisphere

The only regulation of porbeagle catches in the Southern Hemisphere is New Zealand's total allowable catch of 249 tons per year, instituted in 2004.[1] In June 2018 the New Zealand Department of Conservation classified the porbeagle as "Not Threatened" with the qualifier "Threatened Overseas" under the New Zealand Threat Classification System.[60]

Eastern North Atlantic and Mediterranean Sea

In the eastern North Atlantic, porbeagle fishing has been illegal in waters of the European Union since 2011.[50] From 1985 and until the EU ban, the Faroe Islands and Norway (which are not members of the EU) were allowed annual quotas of 200 tons and 125 tons, respectively, from European Community waters. Although these quotas were lower than the originals set in 1982 (500 tons for Norway and 300 tons for the Faroe Islands), they were still consistently higher than the yearly total porbeagle catch in the region, thus had no practical effect.[49] The species is included on the red list of Norway and it has been protected in their national waters since 2012.[51] Any porbeagle caught in EU or Norwegian waters by accident must be released.[50][61]

In the Mediterranean Sea, the porbeagle is on the verge of extinction, with a population decline over 99.99% since the mid-20th century. Its range has contracted to the waters around the Italian Peninsula, where a nursery area may exist. Only a few dozen specimens have been recorded in the past few decades, from scientific surveys, swordfish fishery bycatch, and sport fishers.[57][62] In 1995, it was included in Annex III ("species whose exploitation is regulated") of the Barcelona Convention Protocol on protected areas and biodiversity in the Mediterranean, which has not been ratified. In 1997, it was listed on Appendix III of the Bern Convention (the Convention on the Conservation of European Wildlife and Natural Habitats). However, these listings have yet to result in the implementation of new management plans, despite the recognized need for urgent action.[57]

The European Union prohibits EU vessels from fishing for, retaining, boarding, transhipping, or landing porbeagle sharks in all waters since January 2011.[50] It is subject to a zero total allowable catch in EU waters by any vessel.[63]

Western North Atlantic

The western North Atlantic porbeagle population has a more positive prospect than in the eastern North Atlantic. Fishing in Canadian waters was originally regulated by the 1995 Fisheries Management Plan for pelagic sharks in Atlantic Canada, which established an annual quota of 1,500 tons, restricted the time, place, and gear types allowed for commercial fishing, and set limits for bycatch and recreational fishing. In 2000–2001, Fisheries and Oceans Canada prepared a detailed population model and concluded that a quota of 200–250 tons would allow for population growth, resulting in a quota of 250 tons being adopted for the period of 2002–2007. The mating grounds off Newfoundland were also closed to shark fishing. In 2004, the Committee on the Status of Endangered Wildlife in Canada listed the porbeagle as endangered, largely on the basis of the low population abundance (<25% of original numbers). Canada decided not to list the species under its Species At Risk Act, but further reduced the total fishing quota to 185 tons.[53] In US waters, the 1993 Fishery Management Plan for Sharks of the Atlantic Ocean sets an annual quota of 92 tons (after processing) for the porbeagle.[52] In 2006, this species was listed as a species of concern by the NMFS, meaning that it merits conservation concern, but data are insufficient for inclusion on the US Endangered Species Act.[64]

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Porbeagle: Brief Summary

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The porbeagle or porbeagle shark (Lamna nasus) is a species of mackerel shark in the family Lamnidae, distributed widely in the cold and temperate marine waters of the North Atlantic and Southern Hemisphere. In the North Pacific, its ecological equivalent is the closely related salmon shark (L. ditropis). It typically reaches 2.5 m (8.2 ft) in length and a weight of 135 kg (298 lb); North Atlantic sharks grow larger than Southern Hemisphere sharks and differ in coloration and aspects of life history. Gray above and white below, the porbeagle has a very stout midsection that tapers towards the long, pointed snout and the narrow base of the tail. It has large pectoral and first dorsal fins, tiny pelvic, second dorsal, and anal fins, and a crescent-shaped caudal fin. The most distinctive features of this species are its three-cusped teeth, the white blotch at the aft base of its first dorsal fin, and the two pairs of lateral keels on its tail.

The porbeagle is an opportunistic hunter that preys mainly on bony fishes and cephalopods throughout the water column, including the bottom. Most commonly found over food-rich banks on the outer continental shelf, it makes occasional forays both close to shore and into the open ocean to a depth of 1,360 m (4,460 ft). It also conducts long-distance seasonal migrations, generally shifting between shallower and deeper water. The porbeagle is fast and highly active, with physiological adaptations that enable it to maintain a higher body temperature than the surrounding water. It can be solitary or gregarious, and has been known to perform seemingly playful behavior. This shark is aplacental viviparous with oophagy, developing embryos being retained within the mother's uterus and subsisting on non-viable eggs. Females typically bear four pups every year.

Only a few shark attacks of uncertain provenance have been attributed to the porbeagle. It is well regarded as a game fish by recreational anglers. The meat and fins of the porbeagle are highly valued, which has led to a long history of intense human exploitation. However, this species cannot sustain heavy fishing pressure due to its low reproductive capacity. Direct commercial fishing for the porbeagle, principally by Norwegian longliners, led to stock collapses in the eastern North Atlantic in the 1950s, and the western North Atlantic in the 1960s. The porbeagle continues to be caught throughout its range, both intentionally and as bycatch, with varying degrees of monitoring and management. The International Union for Conservation of Nature (IUCN) has assessed the porbeagle as vulnerable worldwide, and as either endangered or critically endangered in different parts of its northern range.

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Classification

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Lamna nasus (Bonnaterre, 1788)

Reference

Wheeler, A. (1992). A list of the common and scientific names of fishes of the British Isles. J. Fish Biol. 41(Suppl. A): 1-37

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Diet

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Feeds mainly on herring, gaspereau, and mackerels; cod, white hake, red hake, haddock, cusk, and squid are eaten less often.

Reference

North-West Atlantic Ocean species (NWARMS)

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Distribution

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Newfoundland to New Jersey

Reference

North-West Atlantic Ocean species (NWARMS)

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Habitat

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Prefers cool waters, common on continental shelves but have also been found well offshore as well as inshore areas.

Reference

North-West Atlantic Ocean species (NWARMS)

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Habitat

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nektonic

Reference

North-West Atlantic Ocean species (NWARMS)

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