|Scientific Name:||Thunnus obesus|
|Species Authority:||(Lowe, 1839)|
Thunnus mebachi Kishinouye, 1915
Thynnus obesus Lowe, 1839
Thynnus sibi Temminck & Schlegel, 1844
|Red List Category & Criteria:||Vulnerable A2bd ver 3.1|
|Assessor(s):||Collette, B., Acero, A., Amorim, A.F., Boustany, A., Canales Ramirez, C., Cardenas, G., Carpenter, K.E., Chang, S.-K., Chiang, W., de Oliveira Leite Jr., N., Di Natale, A., Die, D., Fox, W., Fredou, F.L., Graves, J., Viera Hazin, F.H., Hinton, M., Juan Jorda, M., Minte Vera, C., Miyabe, N., Montano Cruz, R., Nelson, R., Oxenford, H., Restrepo, V., Schaefer, K., Schratwieser, J., Serra, R., Sun, C., Teixeira Lessa, R.P., Pires Ferreira Travassos, P.E., Uozumi, Y. & Yanez, E.|
|Reviewer(s):||Russell, B. & Polidoro, B.|
This species is important in commercial fisheries around the world. It is being effectively managed throughout the majority of its range, with the exception of the Western and Central Pacific stock. With the exception of the Western Pacific population, all other stocks are being fished below current maximum sustainable yield (MSY). Based on weighted declines of total biomass or spawning stock biomass (SSB) across all stocks, there has been an estimated 42% decline globally over the past 15 years (1992–2007), or three generation lengths. As the MSY of the Western and Central Pacific stock represents more than 20% of the global population, this species is listed as Vulnerable under Criterion A2. In addition, this species may undergo further declines if the mortality of the species in bycatch of the Skipjack fishery cannot be reduced.
|Range Description:||This species is circumglobal in tropical and temperate seas. It is not found in the Mediterranean.|
Native:American Samoa (American Samoa); Angola (Angola); Anguilla; Antigua and Barbuda; Argentina; Aruba; Australia; Bahamas; Barbados; Belize; Bermuda; Bonaire, Sint Eustatius and Saba (Saba, Sint Eustatius); Brazil; Brunei Darussalam; Cambodia; Canada; Cape Verde; Cayman Islands; Chile; China; Christmas Island; Cocos (Keeling) Islands; Colombia; Congo, The Democratic Republic of the; Cook Islands; Costa Rica; Côte d'Ivoire; Cuba; Curaçao; Dominica; Dominican Republic; Ecuador; El Salvador; Equatorial Guinea; Falkland Islands (Malvinas); Fiji; French Guiana; French Polynesia; Gabon; Gambia; Ghana; Grenada; Guadeloupe; Guam; Guatemala; Guinea; Guinea-Bissau; Guyana; Haiti; Honduras; Hong Kong; India; Indonesia; Ireland; Jamaica; Japan; Kenya; Kiribati; Korea, Democratic People's Republic of; Korea, Republic of; Liberia; Madagascar; Malaysia; Maldives; Marshall Islands; Martinique; Mauritania; Mauritius; Mexico; Micronesia, Federated States of ; Montserrat; Morocco; Mozambique; Namibia; Nauru; New Caledonia; New Zealand; Nicaragua; Nigeria; Niue; Norfolk Island; Northern Mariana Islands; Oman; Pakistan; Palau; Panama; Papua New Guinea; Peru; Philippines; Pitcairn; Portugal; Puerto Rico; Réunion; Russian Federation; Saint Barthélemy; Saint Kitts and Nevis; Saint Lucia; Saint Martin (French part); Saint Vincent and the Grenadines; Samoa; Senegal; Seychelles; Sierra Leone; Singapore; Sint Maarten (Dutch part); Solomon Islands; Somalia; South Africa; Spain; Sri Lanka; Suriname; Taiwan, Province of China; Tanzania, United Republic of; Thailand; Timor-Leste; Tokelau; Tonga; Trinidad and Tobago; Turks and Caicos Islands; Tuvalu; United Kingdom; United States; United States Minor Outlying Islands; Uruguay; Vanuatu; Venezuela, Bolivarian Republic of; Viet Nam; Virgin Islands, British; Virgin Islands, U.S.; Wallis and Futuna; Yemen
|FAO Marine Fishing Areas:||
Atlantic – eastern central; Atlantic – northeast; Atlantic – northwest; Atlantic – southeast; Atlantic – southwest; Atlantic – western central; Indian Ocean – eastern; Indian Ocean – western; Pacific – eastern central; Pacific – northeast; Pacific – northwest; Pacific – southeast; Pacific – southwest; Pacific – western central
|Range Map:||Click here to open the map viewer and explore range.|
FAO worldwide reported landings show a gradual increase from 808 tonnes in 1950 to an average of approximately 400,000–450,000 tonnes from 1996–2006 (FAO 2009). There are four stocks that are globally managed for this species. As of 2004, the stocks in the Atlantic and Indian Ocean are considered Fully Exploited, and the Eastern Pacific and Western/Central Pacific stocks are considered Over-exploited (Majkowski 2007). It is assumed that the Bigeye Tuna in the Eastern Pacific comprise a separate stock from the Western Pacific.
Eastern Pacific Ocean
In the Eastern Pacific, annual catches although fluctuating, average 100,000–130,000 tonnes and are increasing. The expansion of the purse seine fisheries in mid 1990s has contributed to this increase in landings (STECF 2007). The stock size in 1993 is estimated to have been 34% of its unexploited size. After 1993, purse seining for tunas associated with fish-aggregating devices (FADs) took significant quantities of small and medium-sized Bigeye Tuna. In 2005, after several years of poor recruitment and excessive levels of fishing mortality, the stock size was estimated to be at about 14% of its unexploited size. Due to recent spikes in recruitment, the current level has increased to 17% (IATTC 2008). Recent catches, such as in 2008, have been above the estimated maximum sustainable yield (MSY) of 84,000 tonnes (ISSF 2010).
Previous analyses indicated that the spawning stock biomass (SSB) was below MSY, and that fishing mortality rates were about 20% greater than those corresponding to the MSY (IATTC 2008, Aires da Silva and Maunder 2007), indicating that the Bigeye Tuna stock in the Eastern Pacific was over-exploited (IATTC 2008). However, according to the most recent stock assessment conducted in 2009 (Aires da Silva and Maunder 2010), fishing mortality rates are estimated to be below the level corresponding to MSY, and the recent levels of spawning biomass are estimated to be above that level (IATTC 2010). However, these results are more pessimistic if a stock-recruitment relationship is assumed, if a higher value is assumed for the average size of the older fish, if lower rates of natural mortality are assumed for adult Bigeye Tuna, and if only the late period of the fishery (1995–2009) is included in the assessment (IATTC 2010). In addition, La Niña events may become stronger and more frequent during the period 2010–2030, and this La Niña dominance may negatively influence recruitment strength of Bigeye Tuna in the Eastern Pacific Ocean (IATTC 2010).
Based on linear regression of SSB estimates from the most recent 2009 stock assessment (Aires da Silva and Maunder 2010), there has been an estimated 18% decline in SSB over the past 15 years (1992–2007) in the Eastern Pacific.
Western and Central Pacific Ocean
The overall trend in the Western Central Pacific Ocean is that biomass declined rapidly during the 1950s and 1960s, was relatively stable through the 1970s and 1980s, and then declined steadily from 1990 onwards (Langley et al. 2008). Adult biomass has declined by at least 20% over the last decade (STECF 2007, Langley et al. 2008). Fishing mortality has increased steadily since the introduction of commercial fishing. Current fishing mortality exceeds FMSY, and it was estimated that a 34–50% reduction from the level of fishing mortality in 2004–2007 would be needed to keep the biomass above the level corresponding to MSY (ISSF 2010). However, current bomass is also greater than BMSY. It was predicted that if fishing mortality continues at current levels, the biomass would be reduced to about half the MSY level (Harley et al. 2010, ISSF 2010).
Based on linear regression of SSB estimates from the most recent 2010 stock assessment (Harley et al. 2010), there has been an estimated 29% decline in SSB over the past 15 years (1992–2007) in the Western and Central Pacific. Currently, this stock is approaching an overfished state, if it is not already slightly overfished (Harley et al. 2010).
In previous assessment conducted in 2005 (Hillary and Mosquiera 2006), spawning stock biomass was estimated to have declined from approximately 180,000 tonnes to about 75,000 tonnes from 1954–2006, and given 2002 levels of fishing mortality and effort, was projected to decline to approximately 50,000 tonnes by 2014 (Hillary and Mosqueira 2006).
Results of an updated assessment conducted in 2009 based on various models (IOTC 2009), showed that results were broadly similar to previous work. Current (2008) exploitation levels for this stock (107,000 t) are within the range of estimated MSY levels (100,000–115,000 t), although catches in the past (1997–1999) have significantly exceeded MSY. Estimated values of fishing mortality and SSB for 2008 are also close to MSY-related values, indicating a fully exploited stock (IOTC 2009). Current spawning stock is estimated to be two billion individuals and 800,000 tonnes (IOTC 2009).
Based on linear regression of SSB estimates from the most recent 2009 stock assessment (IOTC 2009), there has been an estimated 73% decline in SSB over the past 15 years (1992–2007) in the Indian Ocean.
Genetic, tagging and fisheries data suggest this species constitutes a single interbreeding population in the Atlantic. The total catch for this species in the Atlantic increased up to the mid-1970s reaching 60,000 t and fluctuated over the next 15 years. In 1991, catch surpassed 95,000 t and continued to increase, reaching a historic high of about 133,000 t in 1994. Reported and estimated catch has been declining since then and fell below 100,000 t in 2001. This gradual decline in catch has continued, although with some fluctuations from year to year, until the most recent year of data 2009. The preliminary estimate for 2009 is 86,011 t, the highest value in the last five years. This estimate includes preliminary estimates made for a few fleets that have not yet provided data to ICCAT (SCRS ICCAT 2010).
In 2010, the plausible range of MSY estimated from the joint distribution using three types of abundance indices was between 78,700 and 101,600 tons (80% confidence limits) with a median MSY of 92,000 t. Historical estimates show large declines in biomass and increases in fishing mortality, especially in the mid 1990s when fishing mortality exceeded FMSY for several years. In the last five or six years there have been possible increases in biomass and declines in fishing mortality. The biomass at the beginning of 2010 was estimated to be at between 0.72 and 1.34 (80% confidence limits) of the biomass at MSY, with a median value of 1.01 and the 2009 fishing mortality rate was estimated to be between 0.65–1.55 (80% confidence limits) with a median of 0.95 (SCRS ICCAT 2010).
Based on linear regression of total biomass estimates from the most recent 2010 stock assessment (ICCAT 2010), there has been an estimated 40% decline in total biomass over the past 15 years (1992–2007) in the Atlantic Ocean.
|Habitat and Ecology:||
This pelagic and oceanodromous species occurs in waters with temperatures ranging from 13–29°C, but the optimum is between 17°C and 22°C. Variation in occurrence is closely related to seasonal and climatic changes in surface temperature and thermocline. Juveniles and small adults school at the surface in monospecific groups or mixed with other tunas, and may be associated with floating objects. Adults stay in deeper waters (Maigret and Ly 1986). This species is mostly found above 500 m, but can dive deeper. This species feeds on a wide variety of fishes, cephalopods and crustaceans during the day and at night (Collette 1995).
Eggs and larvae are pelagic (Kailola et al. 1993). This species is a multiple spawner that may spawn every one or two days over several months (Nikaido et al. 1992). They spawn over periods of the full moon, and spawn throughout the year in tropical waters (Kailola et al. 1993). Although spawning apparently occurs widely across the equatorial Pacific Ocean, the greatest reproductive potential appears to be in the eastern Pacific, based on apparent maturation, size frequencies, and catch per unit of effort (Kikawa 1966). In the eastern and central Pacific, spawning has been recorded between 15°N and 15°S and between 105–175°W during most months when sea surface temperatures exceeded 24°C with a peak from April through September in the northern hemisphere and between January and March in the southern hemisphere. Spawning is primarily at night between 1900 and 0400 hr. The average mature female spawned every 2.6 days. The estimated mean relative fecundity is 24 oocytes/g body weight. The number of eggs per spawning has been estimated at 2.9–6.3 million (Collette 2010).
Longevity for this species may vary by region. Estimated maximum age for this species in the Western Pacific is 16 years (Farley et al. 2006), in the Indian Ocean is eight years (Tankevich 1982), in the Atlantic Ocean is nine years (Hallier et al. 2005), and in the Eastern Pacific is five years (Schaefer and Fuller 2006).
Age at first maturity is estimated to be about two years (Nootmorn 2004, Farley et al. 2006). However, Calkins (1980) reports a sexual maturity for this species at 100–130 cm at an age of about three years old. Minimum length at sexual maturity for females can be 80–102 cm, and predicted length at 50% maturity of 102–135 cm (approximately 3.5 years of age) has also been reported in different areas. Males tend to dominate the catches over the entire size range (Collette 2010).
The generation length for this species is between 4.4 and five years based on age structure data across different stocks (Collette et al. 2011).
The all-tackle game fish record is of a 197.31 kg fish caught off Cabo Blanco, Peru in 1957 (IGFA 2011) .
|Use and Trade:||This species is an extremely valuable fishery resource especially for the sashimi market.|
Overfishing is occurring primarily in the Western Pacific, with adult biomass having declined about 20% over the past decade (Langley et al. 2008), and if fishing mortality continues at current levels, the biomass is predicted to reduce to about half the MSY level (Harley et al. 2010, ISSF 2010). In addition, this species may undergo further declines if the mortality of the species in bycatch of the Skipjack Tuna fishery cannot be reduced.
In the Pacific, Bigeye Tuna are primarily exploited by longliners from 40°N to 40°S and by purse seiners from 10°N to 20°S. In the Eastern Pacific Ocean there have been substantial changes in the Bigeye Tuna fishery over the last 15 years. Initially, the majority of the Bigeye Tuna catch was taken by longline vessels, but with the expansion of the fishery using fish-aggregating devices (FADs) since 1993, the purse seine fishery has taken an increasing proportion of the Bigeye Tuna catch. The FAD fishery captures smaller Bigeye Tuna, and has therefore reduced the yield per recruit and the maximum sustainable yield (MSY). On average, the fishing mortality of Bigeye Tuna less than four and a half years old has increased substantially since 1993, and that of older fish has increased slightly (IATTC 2008).
In the Indian Ocean, Bigeye Tuna is mainly caught by industrial purse seine and longline fisheries and appears only occasionally in the catches of other fisheries. However, in recent years the amounts of Bigeye Tuna caught by gillnet fisheries are likely to be considerably higher due to the major changes experienced in some of these fleets, notably changes in boat size, fishing techniques and fishing grounds. In recent years catches of Bigeye Tuna in the western Indian Ocean have dropped considerably, especially in areas off Somalia, Kenya and Tanzania and in particular in 2008 and, especially, 2009. The drop in catches is the consequence of a drop in fishing effort in the area of both purse seine and longline fisheries, due to the effect of piracy in the western Indian Ocean region, while catches are increasing in the eastern Indian Ocean probably due to the shift of some longline fleet in the areas because of the piracy activities along the Somalia area (IOTC 2010).
In the Atlantic this stock is exploited by three major gears/fisheries: longline (50–60%), purse seine (25%) and pole-and-line (15%) (ISSF 2010). Although there are a number of data uncertainties, including a lack of data on illegal, unregulated and unreported (IUU) fishing, stock assessment models estimate the MSY to be between 90,000-93,000 tonnes (ISSF 2010). Based on these projections, biomass is expected to rebuild to the MSY level in a few years if catches are maintained at or below 85,000 tonnes. It is important to note the use of high-tech FADs in the Gulf of Guinea and increases in effort due to vessels coming from the Indian Ocean, will increase already high levels of fishing mortality of juvenile Bigeye Tuna.
This species is listed as a highly migratory species in Annex I of the 1982 Convention on the Law of the Sea (FAO Fisheries Department 1994).
In the Pacific, several countries such as Ecuador, Colombia and Peru have created closures for this species. The vast majority of the catch is from Ecuador in this region. SPC made a recommendation to reduce catches in the Pacific. In Taiwan, the fleet has been reduced by 183 Bigeye long-line vessels (which is more than 30% of fishing capacity) (IATTC 2008). As of December 2009, NOAA has put into place catch limits for US pelagic longline fisheries in Western and Central Pacific Ocean for 2009, 2010 and 2011 having determined that the Pacific Ocean population is subject to overfishing. Under this rule, the U.S. will reduce its longline catch of Bigeye Tuna from the 2004 baseline catch of 4,181 metric tons (mt) to 3,763 mt.
In the Atlantic, the Scientific, Technical and Economic Committee for Fisheries (STECF) recommends that the total catch does not exceed 85,000 t (STECF 2009). Recommendation 04-01 also implemented a new, smaller closure for the surface fishing in the area 0–5ºN, 10–20ºW during November in the Gulf of Guinea.
Aires-da-Silva, A. and Maunder, M.N. 2008. Status of bigeye tuna in the eastern Pacific Ocean in 2007. In: Inter-Amer. Trop. Tuna Comm. (ed.), Stock Assess. Rept. 9. Inter-Amer. Trop. Tuna Comm.
Calkins, T.P. 1980. Synopsis of biological data on the bigeye tuna, Thunnus obesus (Lowe, 1839), in the Pacifi c Ocean. In: W.H. Bayliff (ed.), Synopses of biological data on eight species of scombrids, pp. 219-259. Inter-Am. Trop. Tuna Comm. Spec. Rep. 2.
Collette, B.B. 1995. Scombridae. Atunes, bacoretas, bonitos, caballas, estorninos, melva, etc. In: W. Fischer, F. Krupp, W. Schneider, C. Sommer, K.E. Carpenter, V.H. Niem (ed.), Guia para la identification de especies para los fines de la pesca, pp. 1521-1543. FAO, Rome.
Collette, B.B. 2001. Scombridae. In: K.E. Carpenter and V. Niem (eds), The Living Marine Resources of the Western Central Pacific, pp. 3721-3756. FAO, Rome.
Collette, B.B. 2010. Reproduction and Development in Epipelagic Fishes. In: Cole, K.S. (ed.), Reproduction and sexuality in marine fishes: patterns and processes, University of California Press, Berkeley, CA.
Collette, B.B. and Nauen, C.E. 1983. FAO Species Catalogue. Vol. 2. Scombrids of the World: an annotated and illustrated catalogue of tunas, mackerels, bonitos and related species known to date. Food and Agriculture Organization of the United Nations (FAO) Fisheries Synopsis number 125, volume 2.
Collette, B.B., Carpenter, K.E., Polidoro, B.A., Juan-Jorda, M.J., Boustany, A., Die, D.J., Elfes, C., Fox, W., Graves, J., Harrison, L., McManus, R., Minte-Vera, C., Nelson, R., Restrepo, V., Schratwieser, J., Sun, C-L, Brick Peres, M., Canales, C., Cardenas, G., Chang, S.-K., Chiang, W-C, de Oliveira Leite, N., Harwell, H., Lessa, R., Fredou, F.L., Oxenford, H.A., Serra, R., Shao, K.-T., Sumalia, R., Wang, S-P, Watson, R. and Yanez, E. 2011. High value and long life: Double jeopardy for tunas and billfishes. Science 333: 291-292.
Cox, S.P., Martell, S.J.D, Walters, C.J., Essington, T.E., Kitchell, JF, Boggs, C, and Kaplan, I. 2002. Reconstructing ecosystem dynamics in the central Pacific Ocean, 1952–1998. I. Estimating population biomass and recruitment of tunas and billfishes. Can. J. Fish. Aquat. Sci. 59: 1724-1735.
Durand JD, Collet A, Chow S, Guinand B, Borsa P. 2005. Nuclear and mitochondrial DNA markers indicate unidirectional gene flow of Indo-Pacific to Atlantic bigeye tuna (Thunnus obesus) populations, and their admixture off southern Africa. Mar. Biol. 147: 313-322.
Farley JH, Clear NP, Leroy B, Davis TLO, McPherson G. 2006. Age, growth and preliminary estimates of maturity of bigeye tuna, Thunnus obesus, in the Australian region. Australian Journal of Marine and Freshwater Research 57: 713-324.
Garcia, S. 1994. World review of highly migratory species and straddling stocks. Rome.
Hallier, J.P., Stéquert, B., Maury, O. and Bard, F.X. 2005. Growth of bigeye tuna (Thunnus obesus) in the eastern Atlantic Ocean from tagging recapture data and otolith readings. Col. Vol. Sci. Pap. ICCAT 57: 181-194.
IATTC. 2008. The Fishery for Tunas and Billfishes in the Eastern Pacific Ocean in 2007. In: IATTC Document IATTC-78-05 (ed.), IATTC 78th Meeting 23-27 June 2008. Panama.
IATTC. 2010. Scientific Meeting Report. IATTC, 31 August - 3 September, 2010 La Jolla, CA.
ICCAT. 2009. ICCAT Report 2008-2009.
ICCAT. 2010. Report of the 2010 ICCAT Bigeye Tuna Stock Assessment Session. ICCAT, Pasaia, Gipuzkoa, Spain, July 5 to 9, 2010.
ICCAT SCRS. 2010. Report on the Standing Committee on Research and Statistics (SCRS). International Commission for Conservation of Atlantic Tuna, Madrid, Spain October 4-8, 2010.
IGFA. 2014. International Game Fish Association World Record Game Fishes. Three Kings, New Zealand.
Inernational Seafood Sustainability Foundation (ISSF). 2010. Status of the World Fisheries for Tuna. International Seafood Sustainability Foundation.
IOTC. 2010. Report of the Twelfth Session of the IOTC Working Party on Tropical Tunas. IOTC, Victoria, Seychelles. 18-25 October, 2010.
IUCN. 2011. IUCN Red List of Threatened Species (ver. 2011.2). Available at: http://www.iucnredlist.org. (Accessed: 10 November 2011).
Kailola, P.J., Williams, M.J., Stewart, P.C., Reichelt, R.E., McNee, A. and Grieve, C. 1993. Australian fisheries resources. Bureau of Resource Sciences, Canberra, Australia.
Kikawa, S. 1966. The distribution of maturing bigeye and yellowfin and an evaluation of their spawning potential in different areas in the tuna longline grounds in the Pacific. Rep. Nankai Reg.Fish. Res. Lab 23: 131-208.
Langley, A. , J. Hampton , P. Kleiber and S. Hoyle. 2008. Stock assessment of bigeye tuna in the western and central Pacific Ocean, including an analysis of management options. In: Western and Central Pacific Fisheries Commission (eds). Port Moresby, Papua New Guinea.
Lee P-F, Chen I-C, Tzeng W-N. 2005. Spatial and temporal distribution patterns of bigeye tuna )Thunnus obesus) in the Indian Ocean. Zool. Stud. 44(2): 260-270.
Lu H-J, Lee K-T, Lin H-L, Liao C-H. 2001. Spatio-temporal distribution of yellowfin tuna Thunnus albacares and bigeye tuna Thunnus obesus in the tropical Pacific Ocean in relation to large-scale temperature fluctuation during ENSO episodes. Fish. Sci. 67: 1046-1052.
Maigret, J. and Ly, B. 1986. Les poissons de mer de Mauritanie. Centre national de recherches océanographiques et des pêches (Mauritania) and Science Naturales, Compiègne, France.
Majkowski, J. 2007. Global fishery resources of tuna and tuna-like species. FAO Fisheries Technical Paper 483: 54.
Miyabe N. 1994. A review of the biology and fisheries for bigeye tuna, Thunnus obesus, in the Pacific Ocean. FAO Fisheries Technical Paper 336(2): 207-243.
Nikaido, H., N. Miyabe and S. Ueyanagi. 1992. Spawning time and frequency of bigeye tuna, Thunnus obesus. Bulletin of the National Research Institute of Far.
Nootmorn, P. 2004. Reproductive Biology of Bigeye tuna in the eastern Indian ocean. WPTTO 04-05, IOTC proceedings 7: 1-5.
R.M. Hillary and Mosqueira, I. 2006. Assessment of the Indian Ocean bigeye tuna stock using CASAL.
Schaefer, K.M. 2001. Reproductive Biology of Tunas. In: B.A. Block and E.D. Stevens (eds), Tuna: Physiology, Ecology, and Evolution., pp. 225-270. Academic Press, San Diego, California.
Schaefer KM, Fuller DW. 2006. Estimates of age and growth of bigeye tuna (Thunnus obesus) in the eastern Pacific Ocean, based on otolith increments and tagging data. Bulletin of the Inter-American Tropical Tuna Commission 23(2): 35-76.
Schaefer KM, Fuller DW, Miyabe N. 2005. Reproductive biology of bigeye tuna (Thunnus obesus) in the eastern and central Pacific Ocean. Bulletin of the Inter-American Tropical Tuna Commission 23: 1-31.
STECF. 2007. Review of Scientific Advice for 2008: Consolidated Advice on Stocks of Interest to the European Community. Scientific Technical and Economic Committee for Fisheries, Brussels: 333.
STECF. 2009. Review of Scientific Advice for 2010 Part 2. Scientific, Technical and Economic Committee for Fisheries, Vigo, Spain.
Stéquert B, Conand F. 2004. Age and growth of bigeye tuna (Thunnus obesus) in the western Indian Ocean. Cybium 28(2): 163-170.
Sun C-L. 2003. Age-structured catch-at-length analysis of bigeye tuna in the western and central Pacific Ocean. J. Fish. Soc. Taiwan 30(1): 71-89.
Tankevich, P.B. 1982. Age and growth of the bigeye tuna, Thunnus obesus (Scombridae) in the Indian Ocean. Journal of Ichthyology 22(4): 26-31.
Zhu, G., Y. Zhou, L. Xu, and X. Dai. 2009. Growth and mortality of bigeye tuna Thunnus obesus (Scombridae) in the eastern and central tropical Pacific Ocean. Environ. Biol. Fish 85: 127-137.
|Citation:||Collette, B., Acero, A., Amorim, A.F., Boustany, A., Canales Ramirez, C., Cardenas, G., Carpenter, K.E., Chang, S.-K., Chiang, W., de Oliveira Leite Jr., N., Di Natale, A., Die, D., Fox, W., Fredou, F.L., Graves, J., Viera Hazin, F.H., Hinton, M., Juan Jorda, M., Minte Vera, C., Miyabe, N., Montano Cruz, R., Nelson, R., Oxenford, H., Restrepo, V., Schaefer, K., Schratwieser, J., Serra, R., Sun, C., Teixeira Lessa, R.P., Pires Ferreira Travassos, P.E., Uozumi, Y. & Yanez, E. 2011. Thunnus obesus. The IUCN Red List of Threatened Species. Version 2014.3. <www.iucnredlist.org>. Downloaded on 21 December 2014.|
|Feedback:||If you see any errors or have any questions or suggestions on what is shown on this page, please provide us with feedback so that we can correct or extend the information provided|