<<

SRAC Publication No. 7202

VI August 2005 PR

Species Profile Cobia

Jeffrey B. Kaiser and G. Joan Holt1

Cobia, Rachycentron canadum, is the which was cultured. An offshore The are brownish dorsally with a only species in the family Rachycen- cage project in has suc- whitish ventral surface and often tridae. It is also referred to as ling, cessfully grown cobia to market size have alternating light and dark strip- lemon fish and -eater, among since 2003. Research in , ing on their sides. There is a black other common names. The species Mississippi, South Carolina, Texas lateral band running at about eye is distributed worldwide in warm and Virginia has resulted in many level along the length of the body to marine waters, except for the central successful spawns, both natural and the tail. Cobia are thought to live up and eastern Pacific. Cobia are not hormone induced. Grow-out trials to 15 years in the wild. They are abundant and are not heavily fished of juvenile and market-size cobia in opportunistic carnivores that eat commercially. In 2002, worldwide ponds, recirculating systems and many species of fish, crab, shrimp production (the total caught and cul- cages will likely be conducted in the and . Stomach content data tured) was reported to be about future. show that they prefer crustaceans, 10,416 tons, with Taiwan, Pakistan, particularly portunids (swimming Philippines, Brazil and the United Life history ). Arab Emirates listed as the top five Cobia inhabit both coastal and con- Cobia travel alone or in small schools producers. Considered very good tinental shelf waters, and adult fish and are often found near some kind table fare, cobia is a prized catch for have been found in bays and estuar- of structure, whether floating or in both commercial and recreational ies as well as at depths of 3,900 feet the water column. In the Gulf of fishermen, the latter of which (1,200 m). Temperature appears to , anglers often target cobia account for most reported landings be the primary factor in determin- around offshore oil and gas plat- in U.S. waters. Cobia’s rapid growth ing their range; although specimens forms, buoys, artificial reefs, or float- rate, excellent flesh quality, and lim- have been collected in waters from ing debris, and use both lures and ited availability from the wild have 60 to 89 °F (16 to 32 °C), they live bait to entice them to bite. Cobia stimulated research, appear to prefer temperatures above also tend to associate with rays, tur- particularly in the U.S. and Asia. 68 °F (20 °C). Capture data indicate tles and large fish in open waters. As early as 1975, researchers in that, during cooler months of the They often exhibit unusually curious North Carolina collected cobia eggs year throughout their range, cobia behavior and will readily approach a from the wild and reared them suc- either migrate to warmer water in a boat or diver. cessfully. However, it was not until north-south pattern or move farther As spring approaches and water the early 1990s that Taiwan reported offshore to deeper water. Cobia tol- temperatures rise, fishermen antici- captive spawning of cobia. erate a wide range of salinities. pate the “run” of cobia moving Successful efforts in the U.S. fol- Specimens have been collected in north along the eastern coastline of lowed in 1996. Taiwan now has a waters with 22 to 44 ppt salinity the U.S. and northwest along the commercial industry that produced and reared in culture systems down . Cobia is considered nearly 5,000 tons in 2004, most of to 5 ppt. an excellent sport fish that puts up Cobia have elongated bodies and a tenacious fight when hooked. The 1The University of Texas at Austin Marine grow to 6.5 feet (2 m) and annual migration, which usually Science Institute, Fisheries and 135 pounds (61 kg). Females grow begins in March and April in the Laboratory at Port Aransas, Texas. both larger and faster than males. northern Gulf of Mexico, has received even more attention in a depth of 55 feet (17 m), suggest- Culture techniques recent years with sport fishing ing that the young cobia might tournaments that target the have been schooled up near the During the warmer months of the migrating cobia. bottom of the channel (unpub- year, cobia can be caught and lished data). There is little collec- transferred to tanks or ponds to Reproduction in the wild tion data on this size cobia from use as broodstock for spawning the Gulf of Mexico. However, two purposes (Fig. 1). In captivity, Cobia have a protracted reproduc- fish in the size range of 8 to 20 cobia of all sizes adapt fairly quick- tive season that, in U.S. waters, inches (200 to 500 mm SL) were ly to confinement, where they feed generally runs from about April to caught in September of 2004, also voraciously and grow rapidly. In a September. Females multi- in the ship channel in approxi- description of Taiwanese cobia ple times during the season. The mately 45 feet (14 m) of water. So aquaculture, Liao et al. (2004) exact size and age at which cobia for at least part of their pre-adult report producing cobia eggs from are sexually mature varies with life, cobia apparently inhabit 22-pound (10-kg) broodfish raised location; however, research has inshore areas before heading off- in grow-out cages near shore and shown that males are generally 1 shore where most larger fish are in 0.1- to 0.15-acre (400- to 600- to 2 years old and females are 2 to 2 caught. m ) land-based spawning ponds. 3 years old at first spawning. In The ponds are typically designed the Gulf of Mexico, extensive col- lection data indicate that male cobia can reach sexual maturity at approximately 1 year of age and 25 inches (640 mm) fork length (FL), while the smallest female collected that had developing ovaries was 33 inches (834 mm) FL and 2 years of age. Adult fish are thought to form small groups, with spawning tak- ing place in coastal and offshore waters where females release 400,000 to more than 5 million eggs, depending on the size of the fish. Cobia eggs and larvae have been collected at the surface of both estuarine and offshore waters (out to 90 km), and at depths of 10 to 590 feet (3 to 180 m). Most of the larvae collected in the Gulf of Mexico were found from June to September in surface waters with temperatures higher than 77 °F (25 °C) and salinity greater than 27 ppt. In the Gulf of Mexico, small cobia (less than 1.8 inches, 45 mm SL or standard length) have been found both inshore under floating Sargassum weed and 30 to 40 miles offshore. Larger specimens (1.8 to 10 inches, 45 to 250 mm SL) are usually found in coastal waters near inlets, barrier islands and bays. Twenty juvenile cobia (5 to 8 inches, 120 to 200 mm SL) were collected during the summers of 2003 and 2004 in waters 13 to 55 feet deep (4 to 17 m) near Port Aransas, Texas. Interestingly, ten of those fish (all approximately 8 inches, 200 mm SL) were caught in a single trawl in the Corpus Christi ship channel in late August 2003 at Figure 1. 10 to 20 kg cobia broodstock in recirculating tank systems. as 5-foot-deep (1.5-m) flow-through Research in the U.S. has focused pri- Captured cobia can be induced to systems and stocked with about marily on tank spawning of wild- spawn at the desired time by putting 100 adult fish at a sex ratio of 1:1. caught and cultured adult cobia. them through simulated seasons at Cobia are reported to spawn spon- Scientists in several states have pro- regular intervals. In the typical condi- taneously at temperatures of 73 to duced fertilized eggs with varying tioning cycle (Table 1) photoperiod 80 °F (23 to 27 °C). Peak egg pro- degrees of success. Adult cobia can ranges from 10 (winter) to 14 (sum- duction is in spring and fall. be anesthetized and moved fairly mer) hours of daylight and water Fertilized eggs are collected from easily using eugenol (clove oil) at 10 temperature ranges from 68 to 79 °F the surface of the ponds. to 20 ppm. When fish are anes- (20 to 26 °C). Tank spawning gener- Cobia larvae (Fig. 2) are transferred thetized, a cannula (1.0-mm I.D.) ally begins at 13 to 14 hours of day- to “green water” nursery ponds can be used to check gonadal devel- light and 76 to 80 °F (25.5 to 27 °C). where they are reared on opment (Figs. 3 and 4). Spawning is It will continue for several months if nauplii and rotifers until day 20 (sur- induced by manipulating photoperi- these conditions are maintained. This vival of larvae to day 20 is reported od and water temperature. Cobia method of inducing cobia to spawn to be 5 to 10 percent). Then they have spawned multiple times in cov- naturally has allowed scientists to enter a three-stage nursery pond sys- ered, circular, fiberglass tanks 20 extend the spawning season and tem. During the first stage, days 20 feet (6.1 m) in diameter and 5 feet obtain fertilized eggs for 9 months of to 45, the cobia are weaned onto pel- (1.5 m) deep. These tank systems the year thus far. leted floating food, size-graded every should have some sort of biological Researchers in the U.S. have also 4 to 7 days to reduce cannibalism, filtration, a sand filter, and a heat used hormones to induce adult and grown to 2 to 5 g. The second pump large enough to control water cobia caught during their natural stage (days 45 to 75) uses larger temperature throughout the year. spawning season to produce eggs. Both HCG (human chorionic gonadotropin) injected at 275 IU/kg and a slow-release pellet containing salmon GnRHa (gonadotropin-releasing hormone analog) implanted in fish have resulted in spawns. Both of these spawning methods have advan- tages and disadvantages, but the goal is the same—consistent pro- duction of high-quality eggs and larvae for use in the aquaculture industry and research. Cobia eggs are 1.20 to 1.40 mm in diameter, heavily pigmented, and Figure 2. Six-day-old cobia larva. hatch in about 24 hours at 80 to ponds (more than 0.07 acres, 300 m2), where the fish are fed to satia- tion five to six times daily and reared to 30 g. In the final nursery stage (from day 75 to day 150 to 180), the cobia are grown to 1.3 to 2.2 pounds (600 to 1,000 g) either in large ponds or near-shore cages, depending on the operation. These fish are then stocked in grow-out cages for the last stage of production. The reported culture time is 6 to 8 months for a 13- to 22-pound (6- to 10-kg) final product. They are har- vested at a density of about 0.12 pounds per gallon (14 kg/m3). The feed conversion ratio (FCR) with pel- leted diets (crude protein 42 to 45 percent) during grow-out in Taiwan is reported to be about 1.5:1, while the FCR in the Puerto Rico project and in recirculating tank systems is reported to be about 1:1. Figure 3. Anesthesized fish being checked for gonadal development. 84 °F (27 to 29 °C). The fertilized eggs are buoyant and can be gath- ered easily in a recirculating cul- ture system using a side-looped egg collector with an 800-micro- meter mesh bag. After collection, the eggs are counted (approximate- ly 420 eggs/ml) volumetrically using graduated cylinders, which also allow separation of viable (floating) and nonviable eggs. Eggs are usually stocked into rearing tanks at a density of 5 to 10 per L, although this phase of cobia pro- duction is still being researched in order to optimize yield per tank. Researchers in the U.S. and Taiwan have had difficulty raising cobia lar- vae at high densities, and the typical tank harvest yields one cobia (2.75 inches, 7 cm, 1g) per liter at 40 days Figure 4. Reviving anesthetized fish. post-hatch. Larvae in tanks are fed enriched rotifers 3 to 5 rotifers/ml) beginning on the third day post- hatch and continuing for a minimum Table 1. Typical photoperiod and temperature regime used for of 4 days. Enriched Artemia prepara- cobia broodstock tanks at the University of Texas Fisheries and tions are fed from that point until Mariculture Laboratory. Each interval listed below represents weaning (generally day 25 to 30), approximately 2 weeks. after which the cobia are given only dry feed (Fig. 5). Photoperiod Some juveniles reared in recircu- (hours light - hours dark) Water temperature (°C) lating raceway systems have 13-11 25 reached 8.8 pounds (4 kg) in 1.5 years when fed a commercially 13-11 25 available floating pellet. 12-12 24 Dissolved oxygen levels must be 12-12 24 maintained during all stages of cul- ture. Cobia show signs of stress at 11-13 23 levels below 5 mg/L (ppm). They 11-13 23 require warm water for optimal 10-14 22 growth, preferably warmer than 79 °F (26 °C), so temperature dur- 10-14 21 ing grow-out is critical when deter- 10-14 20 mining where to locate production facilities or cages. Other than 11-13 21 reports from Taiwan, there is very 11-13 22 little information about cobia pro- duction beyond this stage. The pro- 12-12 23 tein and lipid requirements, rearing 12-12 23 density, and salinity tolerance of juveniles are all being investigated 13-11 24 in the U.S. with the hope that large- 13-11 24 scale domestic production of cobia will be a reality in the near future. 13-11 25 One of the most critical aspects of 14-10 26 cobia production is the transporta- Continue the 14-10 photoperiod and 26-27 °C temperature to maintain tion of juvenile fish. Dissolved spawning. oxygen levels, shipping density, and handling stress are just some of the factors that must be con- trolled by both the shipping and receiving facilities. A commercial Conclusion Cobia culture worldwide is just beginning and shows great poten- tial for expansion. Cobia’s phe- nomenal growth rate, good flesh quality, and good feed conversion rates are desirable aquaculture characteristics. The expansion of Taiwanese cobia production in the last 5 years demonstrates that the species can be raised profitably. Other countries in Asia are likely to begin producing significant quantities of cobia in coming Figure 5. Summary of larval cobia feeding regime used at the University of years. Production in and near the Texas Fisheries and Mariculture Laboratory. Note: Both rotifers and Artemia U.S. is slowly developing, primari- are enriched with a commercially available preparation. ly in the , as investors and aquaculturists investigate the species’ potential. Continued producer of cobia in the U.S. lems than fish in offshore grow-out research with recirculating sys- reports packing fish at a density of sites. Cultured cobia will certainly tems, pond grow-out, and offshore 0.08 pounds per gallon (10 g need to be monitored and disease cage culture could offer producers fish/L) for live-haul trucking (less outbreaks treated if the species is to alternative production techniques than 24 hours) and 4 to 5 g fish/L be cultured successfully. for cobia. Controlled spawning, for overseas air transport. larval and juvenile rearing, and Marketing and economics grow-out of cobia have all been Diseases Cobia is considered an excellent successfully demonstrated. Global Although cobia is a fairly hardy table fish, but because the volume production is projected to increase species, the fish are susceptible to of product in the market is low, in the future. the parasites, bacteria and viruses many consumers have probably that typically affect other warm- never tasted cobia. If it were wide- Suggested Readings water marine species. Bacterial dis- ly available through aquaculture, Arnold, C. R., J. B. Kaiser and G. J. eases that affect cobia include pas- potential markets for its firm, white Holt. 2002. Spawning of cobia teurellosis (caused by Photobacterium meat could be developed. Rachycentron canadum in captivity. damselae subsp. piscicida), vibriosis Journal of the World Aquaculture The Taiwanese report producing Society, 33(2):205-208. and streptococcosis. The viral dis- both a 13- to 17-pound (6- to 8-kg) ease lymphosystis and the parasites market size fish for export to Japan Benetti, D. D., J. F. Alarcon, O. M. Stevens, B. O’Hanlon, J. A. myxosporidea, Trichodina and and a 17- to 22-pound (8- to 10-kg) Neobenedenia also cause problems. Rivera, G. Banner-Stevens and F. fish for domestic consumption; J. Rotman. 2003. Advances in Because cobia are a very active, processed fillets also are exported. hatchery and growout technology rapidly growing species, any The current market value in Taiwan of marine finfish candidate pathogen that interrupts or reduces for cobia 17 pounds (8 kg) and larg- species for in the transfer of oxygen across the gills er is about $2.50 US per pound the Caribbean. Proceedings of the can be especially devastating. The ($5.50 per kg), with smaller fish Gulf and Caribbean Fisheries parasite Amyloodinium is a particular bringing less. The cost of producing Institute 54, pp. 475-487. problem. It kills juvenile cobia with- cobia in Taiwan is estimated to be Brown-Peterson, N. J., R. M. in days if left untreated. Afflicted $1.10 US per pound ($2.40 per kg) Overstreet, J. M. Lotz, J. S. Franks fish typically exhibit flashing or live weight, which is low compared and K. M. Burns. 2001. scratching behavior, coughing, or a to several other species. Reproductive biology of cobia, reluctance to feed. Because of its Rachycentron canadum, from Prices for cobia produced in coastal waters of the southern resilient nature and high reproduc- Puerto Rico and shipped to Miami tive rate, this parasite can be espe- United States. Fishery Bulletin, whole and gutted are about $3.00 99:15-28. cially destructive in recirculating cul- to $4.00 US per pound ($6.50 to ture systems. Chen, S. C., R. J. Kou, C. T. Wu, P. C. $9.00 US per kg) for 13- to 15- Wang and F. Z. Su. 2001. Mass Improved production strategies pound (6- to 7-kg) fish. There is mortality associated with a could alleviate some of the disease also a market for weaned juveniles Sphaerospora-like myxosporidean and parasite problems in the cage for stocking into grow-out systems. infestation in juvenile cobia, production of cobia. In Taiwan it In the U.S., juveniles 1 to 1.5 g are Rachycentron canadum (L.), marine was noted that fish in near-shore available for part of the year at a cage cultured in Taiwan. Journal of cages in protected areas with less price of $1.00 to $2.50 each, Fish Diseases, 24(4):189-195. water flow had more disease prob- depending on the amount ordered. Chou, R. L., M. S. Su and H. Y. Chen. Hassler, W. W. and R. P. Rainville. Meyer, G. H. and J. S. Franks. 1996. 2001. Optimal dietary protein and 1975. Rachycentron canadum, Food of cobia, Rachycentron canad- lipid levels for juvenile cobia through larval and juvenile stages. um, from the north cental Gulf of (Rachycentron canadum). University of North Carolina Sea Mexico. Gulf Research Reports, Aquaculture, 193:81-89. Grant College Program. UNC-SG- 9:161-167. Chou, R. L., B. Y. Her, M. S. Su, G. 75-30. Raleigh, North Carolina. Resley, M. R. 2004. Growth and sur- Hwang, Y. H. Wu and H. Y. Chen. Kaiser, J. B. and G. J. Holt. 2004. Cobia: vival of juvenile cobia (Rachycentron 2004. Substituting fish meal with A new species for aquaculture in canadum) at different salinities. MS soybean meal in diets of juvenile the U.S. World Aquaculture Thesis, Texas A&M University at cobia Rachycentron canadum. Magazine, 35(2):12-14. Corpus Christi. Corpus Christi, Aquaculture, 229:325-333. Texas. Kilduff, P., W. DuPaul, M. Osterling, J. Dawson, C. E. 1971. Occurrence and Olney, Jr. and J. Tellock. 2002. Shaffer, R. V. and E. L. Nakamura. description of prejuvenile and early Induced tank spawning of cobia, 1989. Synopsis of Biological Data juvenile Gulf of Mexico cobia, Rachycentron canadum, and early on the Cobia Rachycentron canad- Rachycentron canadum. Copeia, larval husbandry. World Aquacul- um (Pisces:Rachycentridae). FAO 1971(1):65-71. ture Magazine, 33(2):35-38. Fisheries Synopsis 153 (National Marine Fisheries Service/S 153), Denson, M. R., K. R. Stuart, T. I. J. Liao, I. C., T. S. Huang, W. S. Tsai, C. U.S. Department of Commerce, Smith, C. R. Weirich and A. M. Hsueh, S. L. Chang and E. M. NOAA Technical Report National Segars. 2003. Effects of salinity on Leano. 2004. Cobia culture in Marine Fisheries Service 82. growth, survival, and selected Taiwan: current status and prob- Washington, D.C. hematological parameters on juve- lems. Aquaculture, 237:155-165. nile cobia, Rachycentron canadum. Stevens, O., J. Alarcon and G. Banner- Liu, P. C., J. Y. Lin and K. K. Lee. Journal of the World Aquaculture Stevens. 2004. ACFK: Cobia finger- 2003. Virulence of Photobacterium Society, 34(4):496-504. ling update. Global Aquaculture damselae subsp. piscicida in cul- Advocate, 7(1):46-47. Ditty, J. G. and R. F. Shaw. 1992. tured cobia Rachycentron canadum. Larval development, distribution, Journal of Basic Microbiology, Su, M. S., Y. H. Chien and I. C. Liao. and ecology of cobia Rachycentron 43(6):499-507. 2000. Potential of marine cage canadum (Family:Rachycentridae) aquaculture in Taiwan: Cobia cul- Liu, P. C., J. Y. Lin, P. T. Hsiao and K. in the northern Gulf of Mexico. ture. pp. 97-106 in I. C. Liao and K. Lee. 2004. Isolation and charac- Fishery Bulletin, 90:668-677. C. K. Lin, editors. Cage terization of pathogenic Vibrio algi- Aquaculture in Asia. Asian Faulk, C. K. and G. J. Holt. 2003. Lipid nolyticus from diseased cobia Fisheries Society, Manila, and Nutrition and feeding of cobia Rachycentron canadum. Journal of World Aquaculture Society- Rachycentron canadum larvae. Basic Microbiology, 44(1):23-28. Journal of the World Aquaculture Southeast Asian Chapter, Bangkok. Lopez, C., P. R. Rajan, J. H. Y. Lin, T. Society, 34(3):368-378. Su, M. S. and I. C. Liao. 2001. Present Y. Kuo and Huey-Lang Yang. 2002. status and prospects of marine Faulk, C. K. and G. J. Holt. In Press. Disease outbreak in seafarmed cage aquaculture in Taiwan. pp. Advances in rearing cobia cobia (Rachycentron canadum) asso- 193-201 in I. C. Liao and J. Baker, Rachycentron canadum larvae in ciated with Vibrio spp., Photobac- editors. Aquaculture and Fisheries recirculating aquaculture systems: terium damselae ssp. piscicida, Resource Management. TFRI live prey enrichment and greenwa- monogenean and myxosporean Conference Proceedings, vol. 4. ter culture. Aquaculture. parasites. Bulletin of the European Taiwan Fisheries Research Association of Fisheries Pathology, Franks, J. S., J. T. Ogle, J. M. Lotz, L. Institute, Keelung, Taiwan. C. Nicholson, D. N. Barnes and K. 22(3):206-211. Weirich, C. R., T. I. J. Smith, M. R. M. Larson. Spontaneous spawning Lotz, J. M., R. M. Overstreet and J. S. Denson, A. D. Stokes and W. E. of cobia, Rachycentron canadum, Franks. 1996. Gonadal maturation Jenkins. 2004. Pond culture of larval induced by human chorionic in the cobia, Rachycentron and juvenile cobia, Rachycentron gonadotropin (HCG), with com- canadum, from the north central canadum, in the southeastern ments on fertilization, hatching, Gulf of Mexico. Gulf Research United States: Initial observations. and larval development. Reports, 9:147-159. Journal of Applied Aquaculture Proceedings of the Gulf and , Caribbean Fisheries Institute, 16(1/2):27-44. 52:598-609.

SRAC fact sheets are reviewed annually by the Publications, Videos and Computer Software Steering Committee. Fact sheets are revised as new knowledge becomes available. Fact sheets that have not been revised are considered to reflect the current state of knowledge.

The work reported in this publication was supported in part by the Southern Regional Aquaculture Center through Grant No. 2003-38500-12997 from the United States Department of Agriculture, Cooperative State Research, Education, and Extension Service.