|Scientific Name:||Alopias pelagicus|
|Species Authority:||Nakamura, 1935|
|Taxonomic Source(s):||Chen, X., Xiang, D., Ai, W., and Shi, X. 2015. Complete mitochondrial genome of the pelagic thresher Alopias pelagicus (Lamniformes: Alopiidae). Mitochondrial DNA 26(2): 323-324.|
|Red List Category & Criteria:||Vulnerable A2d+4d ver 3.1|
|Assessor(s):||Reardon, M., Márquez, F., Trejo, T. & Clarke, S.C.|
|Reviewer(s):||Fowler, S.L., Dudley, S., Soldo, A., Dulvy, N.K. & SSG Pelagic Shark Red List Workshop participants (Shark Red List Authority)|
All members of genus Alopias, the thresher sharks, are listed as Vulnerable globally because of their declining populations. These downward trends are the result of a combination of slow life history characteristics, hence low capacity to recover from moderate levels of exploitation, and high levels of largely unmanaged and unreported mortality in target and bycatch fisheries.
The Pelagic Thresher Shark (Alopias pelagicus) is a large, wide-ranging Indo-Pacific Ocean pelagic shark, apparently highly migratory, with low fecundity (two pups/litter) and a low (2-4%) annual rate of population increase. This species is especially vulnerable to fisheries exploitation (target and by-catch) because its epipelagic habitat occurs within the range of many largely unregulated and under-reported gillnet and longline fisheries, in which it is readily caught. Although this species is reportedly relatively common in some coastal localities, current levels of exploitation in some areas are considered to be unsustainable. Overall, it is considered highly likely that serious depletion of the global population has occurred.
|Range Description:||Oceanic and wide-ranging in the Indo-Pacific, Indian Ocean: South Africa (Kwa-Zulu Natal), Red Sea, Gulf of Aden, Arabian Sea (off Somalia, between Oman and India, and off Pakistan), Australia (northwest Western Australia). Western North Pacific: China, Taiwan, Japan (southeastern Honshu). Western South Pacific: New Caledonia, eastern Micronesia, Tahiti. Central Pacific: Hawaiian Islands, equatorial waters north of Howland and Baker, Phoenix and Palmyra Islands. Eastern Pacific: USA (California) and the EEZ of Mexico including the Gulf of California), equatorial waters northwest of French Polynesia, and off Galapagos Islands (Compagno 2001).|
Native:Australia (Northern Territory, Queensland, Western Australia); China; Ecuador (Galápagos); Egypt (Egypt (African part)); Eritrea; French Polynesia; India; Indonesia; Iran, Islamic Republic of; Japan (Honshu); Kenya; Madagascar; Mexico; Micronesia, Federated States of ; Mozambique; New Caledonia; Oman; Pakistan; Saudi Arabia; Somalia; South Africa (Eastern Cape Province, KwaZulu-Natal); Sri Lanka; Sudan; Swaziland; Taiwan, Province of China; Tanzania, United Republic of; United States (California, Hawaiian Is.); Yemen (Socotra, South Yemen)
|FAO Marine Fishing Areas:|
Indian Ocean – western; Indian Ocean – eastern; Pacific – northwest; Pacific – southwest; Pacific – western central; Pacific – southeast; Pacific – eastern central
|Range Map:||Click here to open the map viewer and explore range.|
|Population:||Few population data are available for the Pelagic Thresher throughout its epipelagic range. It is unknown whether its Indian Ocean and Pacific Ocean populations are partly isolated. It is very likely that this species migrates between Central America and the Gulf of California.|
An ongoing population genetic study of A. pelagicus using DNA sequences from the mitochondrial control region indicates gene flow between populations in Mexico and Ecuador (Trejo 2004). However, there is a significant degree of population structure between Taiwan and both populations (Mexico and Ecuador) studied in the Eastern Pacific.
|Current Population Trend:||Decreasing|
|Habitat and Ecology:||This species is poorly known. It is probably highly migratory and is epipelagic from the surface to at least 152 m depth (Compagno 2001). Factors such as temperature and oceanic currents influence its distribution, for example it is found near the Equator in winter, but not in summer (Dingerkus 1987). Its food preference includes squid.|
The Pelagic Thresher Shark is aplacentally viviparous with oophagy, and a litter size of only two very large (158-190 cm) pups. In Ecuador, length at sexual maturity is reported at 140 cm precaudal length (PL) for males and 144 cm PL for females (J. Martinez per. comm.). Age at maturity near Taiwan is estimated as 8-9.2 years in females and 7-8 years in males (Liu et al. 1999). It reaches a maximum length of 330 cm. In the EEZ of Mexico, the breeding season ranges from October to March (Mendizabal-Oriza et al. 2000). Its potential annual rate of population increase under sustainable fishing is thought to be very low and has been estimated at 2-4% (S. Smith pers. comm.), or 0.033 (Dulvy et al. 2008), (compared with the Common Thresher, which is between 4 and 7% (Smith et al. 1998) or 0.254 (Dulvy et al. 2008).
|Movement patterns:||Full Migrant|
|Use and Trade:||
The species is utilized for its meat, liver oil, and hides for leather and fins for shark-fin soup.
Coastal longline fishermen off the coast of Japan report that they retain thresher sharks preferentially over other sharks because of their lower urea content. One fisherman cited values of US$250 per shark for thresher shark carcasses (Gilman et al. 2007).
Thresher shark species (including A. pelagicus) were found to represent at least 2-3% of the fins auctioned in Hong Kong, the world's largest shark fin trading center (Clarke et al. 2006a). Thresher shark fins are generally low value compared to other species because of their low fin ray count (S. Clarke unpubl. data). It is estimated that between 350,000 and 3.9 million thresher sharks (Alopias spp.) are represented in the shark fin trade each year or, in biomass, 12,000 to 85,000 mt (Clarke et al. 2006b).
Members of the genus Alopias, thresher sharks, are threatened from a combination of slow life history characteristics, hence low capacity to recover from moderate levels of exploitation, and high levels of largely unmanaged and unreported mortality in target (for fins and their valuable meat) and bycatch fisheries.
Thresher shark species (including A. pelagicus) were found to represent at least 2-3% of the fins auctioned in Hong Kong, the world's largest shark fin trading center (Clarke et al. 2006a). Thresher shark fins are generally low value compared to other species because of their low fin ray count (S. Clarke unpubl. data). It is estimated that between 350,000 and 3.9 million thresher sharks (Alopias species) are represented in the shark fin trade each year or, in biomass, 12,000-85,000 mt (Clarke et al. 2006b). These estimates are 1-2 orders of magnitude higher than catches of Alopiidae reported to FAO, which since the early-1980s have generally been less than 1,600 tonnes, and around 1,000 mt since 1998 (Maguire et al. 2006), Catches of thresher sharks are clearly hugely under reported globally. Although trend data are as a result largely lacking, these fisheries are unlikely to be sustainable. A recent FAO analysis states, "unless demonstrated otherwise, it is prudent to consider these species as being fully exploited or overexploited globally" (Maguire et al. 2006).
Alopias pelagicus has a particularly low (2-4%) annual rate of population increase, which renders it particularly at risk from depletion in fisheries. It is subject to high levels of bycatch mortality from tuna fisheries and is a target of some smaller shark fisheries, for example in the Gulf of California, Red Sea and possibly Southeast Asia. Underreporting of catches means that trend data for this species are largely lacking, but data available for the Common Thresher (A. vulpinus), which is significantly more fecund and resilient to fisheries, indicate declines in CPUE as high as 80% in the northeast Atlantic over two decades (Baum et al. 2003).
Sharks have been fished heavily by pelagic fisheries operating in the Indian Ocean and significant reductions are thought to have occurred there as a result of intensive pelagic fishing effort (Compagno, L.J.V. pers. comm.). The area of these fishing operations included known pelagic thresher ranges, and this species is especially vulnerable to fisheries exploitation as it is readily caught in gillnets and on longlines, even getting its tail caught in the nets or on hooks. Alopias pelagicus is a known bycatch of the Spanish longline fleet targeting swordfish in the Indian Ocean (IOTC 2000). It has been fished by longline in the northwestern Indian Ocean, and is or has been caught in large numbers in the Red Sea and the Gulf of Aden.
In Indonesia, and probably elsewhere in Southeast Asia, A. pelagicus are caught in very high numbers by tuna longliners throughout the region, especially south Java where they fish in or close to Australian waters (W. White pers. comm.).
The species is also fished in the Central Pacific and is currently an important catch off Taiwan, with about 222 t landed annually. A spawner-per-recruit (SPR) analysis of A. pelagicus in eastern Taiwanese waters suggests mean SPR of pelagic thresher for 1990-2004 was below the biological reference point (BRP) of SPR = 35% suggesting that this stock was slightly overexploited. The authors concede that this assumes a single stock, a hypothesis that cannot yet be accepted or refuted (Liu et al. 2006). This work also provided an untuned Virtual Population Analysis which indicated that the abundance of pelagic thresher stock decreased from 141,398 in 1990 to the lowest level of 97,551 in 2000, and increased thereafter to 153,331 in 2003 (Liu et al. 2006). However, the trend of abundance could not be validated with catch per unit effort series because fishing effort data were not available (Liu et al. 2006). The low population growth rate of this species means that the increase to 2003 could not have been caused by recruitment to a closed stock.
Japanese assessment of data from research longline surveys in the Pacific and Indian Oceans suggests that thresher shark (Alopias species) catch per unit effort increased in the 1990s (to near one shark per 1,000 hooks) over levels in the 1970s (near zero sharks per 1,000 hooks). However, this result is thought to be possibly attributable to an increase in hook depths in the latter period. In recent years, based on logbook data, recorded Japanese catches of thresher sharks worldwide ranged from 252 to 596 mt with an average of 347 mt. The resource is considered stable with no management action required other than ongoing monitoring (Japan Fisheries Agency 2006).
Pelagic Thresher is caught by shark fishermen in large numbers in the Gulf of California and the Pacific coast of Mexico. It is taken off Central America by artisanal fisheries and the local tuna fleet. Ward and Myers (2005) estimated the biomass of thresher sharks to be approximately 5% of the virgin biomass and estimated a decline in abundance of 83% in the East tropical Pacific (within the three generation period). These estimates were made by a comparison of pelagic longline research surveys in the 1950s carried out in the tropical Pacific Ocean with recent data (1990s) collected by observers on pelagic longline fishing vessels, which have been standardized to account for differences in depth and soak time (Ward and Myers 2005).
When A. pelagicus occurs off the west coast of the USA during El Niño years, females comprise 83% of the catch, of which 41% are pregnant. This aggregating of females may possibly make them additionally vulnerable to entangling gear such as gillnets (S. Smith pers. comm.).
Off the Pacific coast of Mexico, Pelagic Threshers are bycatch of the pelagic longline fishery west of Baja California Sur and the opening of the Sea of Cortez down to the southern Mexican border. Unstandardised catch rates are relatively high with around three individuals caught 100 hooks (Mendizábal-Oriza et al. 2000). In addition to being caught in the high seas pelagic longline fishery this species is also caught in inshore coastal gillnets and longlines and offshore (but not oceanic) longlines and gillnets (Mendizábal-Oriza et al. 2000). Analysis of longline data from the EEZ of Mexico's Pacific coast (from 1986-1999) shows that A. pelagicus represented 33% of the sharks and 19% of the total catch of all large pelagics. There is an apparent negative trend in the CPUE (No/100 hooks) from 1986-1999, but these data have not been standardized in order to determine the statistical significance of this trend. This trend is unreported and the data source is unknown. Recently, this fleet (now with fewer longliners) has moved towards the west coast of Baja California and Blue Shark is currently the most important species caught.
In the principal port in Ecuador, Manta, a total of 150,321 individual sharks have been landed between 2003 and 2006, of this A. pelagicus comprised 36%, with A. supercilious comprising 3%. Therefore A. pelagicus make-up 92% of thresher shark landings here.
This species is mainly taken on the high seas, outside waters managed by coastal States. Family Alopiidae is listed as a highly migratory species under the 1995 UN Agreement on the Conservation and Management of Straddling Fish Stocks and Highly Migratory Fish Stocks (UNFSA). The Agreement specifically requires coastal States and fishing States to cooperate and adopt measures to ensure the conservation of these listed species. To date, there is little progress in this regard. See http://www.unclos.com for further details.
The FAO International Plan of Action for the Conservation and Management of Sharks (IPOA-Sharks) recommends that Regional Fisheries Organisations (RFO) carry out regular shark population assessments and that member States cooperate on joint and regional shark management plans. This is of particular importance for pelagic sharks such as Alopias pelagicus whose stocks are exploited by more than one State on the high seas. Although steps are being taken by some RFOs to collect species-specific data on pelagic sharks, and to ban the practise of shark finning (the removal of fins and discard of carcasses at sea), to date no RFO has limited shark catches or drafted a "Shark Plan" as suggested in the IPOA-Shark guidelines. It is widely recognised that shark catch statistics submitted to RFOs by Contracting Parties do not represent the total removals of sharks and are also very limited with respect to the size-, age- and sex- composition of the catch. Much greater monitoring and research investments directed at sharks in particular, and other by-catch species in general, need to be made by the Parties.
Precautionary adaptive collaborative management by regional fisheries organizations and fishing States of target and bycatch fisheries is urgently needed for this biologically and behaviourally vulnerable shark.
The Convention on Migratory Species (CMS) is developing an agreement for the collaborative management of migratory shark species. This may be a useful supplement to traditional fisheries management measures, particularly since the latter are largely not being applied to pelagic shark stocks.
This animal requires careful monitoring because of its limiting life-history traits and the evidence of declines in parts of its range, although available data are currently insufficient to assess the global status of this species. The highly migratory nature of this species could cause seasonal fluctuations in catches or CPUE. However, for proper interpretation of the status of A. pelagicus, analyses combining CPUE from fleets operating in both international waters and within the EEZ of countries where A. pelagicus is captured should be performed as a matter of urgency.
Cailliet, G.M. and Bedford, D.W. 1983. The biology of three pelagic sharks from California waters, and their emerging fisheries: a review. California Cooperative Oceanic Fisheries Investigations Reports.
Clarke, S.C., McAllister, M.K., Milner-Gulland, E.J., Kirkwood, G.P., Michielsens, C.G.J., Agnew, D.J., Pikitch, E.K., Nakano, H. and Shivji, M.S. 2006. Global estimates of shark catches using trade records from commercial markets. Ecology Letters 9: 1115-1126.
Clarke, S., Magnusson, J.E., Abercrombie, D.L., McAllister, M. and Shivji, M.S. 2006. Identification of shark species composition and proportion in the Hong Kong shark fin market using molecular genetics and trade records. Conservation Biology 20: 201-211.
Compagno, L.J.V. 2001. 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). FAO, Rome.
Compagno, L.J.V. FAO species catalogue. Vol. 2. Sharks of the world. An annotated and illustrated catalogue of shark species known to date. Bullhead, Mackerel and Carpet Sharks (Heterodontiformes, Lamniformes & Orectolobiformes).
Dingerkus, G. 1987. Shark distribution. In: Dingerkus, G. (ed.), Sharks, pp. 36-49. Facts on File Publications, New York.
Gilman, E., Clarke, S., Brothers, N., Alfaro-Shigueto-J., Mandelman, J., Mangel, J., Piovano, S., Peterson, S., Watling, D. and Dalzell, P. 2007. Strategies to Reduce Shark Depredation and Unwanted Bycatch in Pelagic Longline Fisheries: Industry Practices and Attitudes, and Shark Avoidance Strategies. Western Pacific Regional Fishery Management Council, Honolulu, USA.
Gilmore, R.G. 1993. Reproductive biology of lamnoid sharks. Environmental Biology of Fishes 38: 95-114.
IOTC (Indian Ocean Tuna Commission). 2000. A general overview on the activity of the Spanish surface longline fleet targeting swordfish (Xiphias gladius) in the Indian Ocean for the period 1993-1999. IOTC Proceedings no. 3.
IUCN. 2009. IUCN Red List of Threatened Species (ver. 2009.2). Available at: www.iucnredlist.org. (Accessed: 3 November 2009).
IUCN SSC Shark Specialist Group. Specialist Group website. Available at: http://www.iucnssg.org/.
Japan Fisheries Agency. 2006. The current status of international fisheries resources [in Japanese]. Fisheries Agency/Fisheries Integration Research Center.
Liu, K.-M., Changa, Y.-T., Ni, I.-H. and Jin, C.-B. 2006. Spawning per recruit analysis of the pelagic thresher shark, Alopias pelagicus, in the eastern Taiwan waters. Fisheries Research 82: 52-64.
Liu, K.M., Chen, C.-T., Liao, T.-H. and Joung, S.-J. 1999. Age, growth, and reproduction of the pelagic thresher shark, Alopias pelagicus in the Northwestern Pacific. Copeia 1999(1): 68-74.
Maguire, J.-J., Sissenwine, M.P., Csirke, J., Grainger, R.J.R. and Garcia, S.M. 2006. The state of world highly migratory, straddling and other high seas fisheries resources and associated species. Fisheries Technical Report. FAO, Rome.
Mendizábal-Oriza, D., Vélez-Marín, R., Márquez-Farías, J.F. and Soriano-Velásquez, S.R. 2000. Tiburones oceanicos del Pacifico de México. Sustentabilidad y Pesca Responsable en México: Evaluación y Manejo. INP. SEMARNAP.
Moteki, M., Arai, M., Tsuchiya, K. and Okamoto, H. 2001. Composition of piscine prey in the diet of large pelagic fish in the eastern tropical Pacific Ocean. Fisheries Science 67: 1063-1074.
Nakamura, H. 1935. The two species of thresher shark from Formosan waters. Memoirs of the Faculty of Science and Agriculture. Taihoku Imperial University 14(1): 1-6.
Otake, T. and Mizue, K. 1981. Direct evidence for oophagy in thresher shark, Alopias pelagicus. Japanese Journal of Ichthyology 28(2): 171-172.
Smith, S.E., Au, D.W. and Show, C. 1998. Intrinsic rebound potentials of 26 species of Pacific sharks. Marine and Freshwater Research 49(7): 663-678.
Strasburg, D.W. 1958. Distribution, abundance, and habits of pelagic sharks in the Central Pacific Ocean. Fisheries Bulletin 58: 335-361.
Trejo, T. 2004. Global population structure of thresher sharks (Alopias spp.) based upon mitochondrial DNA control region sequences. M.Sc. Thesis, Moss Landing Marine Laboratories.
Ward, P. and Myers, R.A. 2005. Shifts in open ocean fish communities coinciding with the commencement of commercial fishing. Ecology 86(4): 835-847.
|Citation:||Reardon, M., Márquez, F., Trejo, T. & Clarke, S.C. 2009. Alopias pelagicus. The IUCN Red List of Threatened Species 2009: e.T161597A5460720.Downloaded on 27 June 2017.|
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