15. Darden, T.L., Walker, M.J., Brenkert, K., Yost, J.R., & Denson, M.R. (2014). Populationgenetics of Cobia (<strong>Rachycentron</strong> <strong>canadum</strong>): implications for fishery management along the coast ofthe southeastern United States. Fishery Bulletin, 112(1), 24-35.Cobia (<strong>Rachycentron</strong> <strong>canadum</strong>) is a pelagic, migratory species with a transoceanic distribution intropical and subtropical waters. Recreational fishing pressure on Cobia in the United States hasincreased substantially during the last decade, especially in areas of its annual inshore aggregations,making this species potentially susceptible to overfishing. Although Cobia along the Atlantic andGulf coasts of the southeastern United States are currently managed as a single fishery, the geneticcomposition of Cobias in these areas is unclear. On the basis of a robust microsatellite data set fromcollections along the U.S. Atlantic coast (2008-09), offshore groups were genetically homogenous.However, the 2 sampled inshore aggregations (South Carolina and Virginia) were geneticallydistinct from each other, as well as from the offshore group. The recapture of stocked fish withintheir release estuary 2 years after release indicates that some degree of estuarine fidelity occurswithin these inshore aggregations and supports the detection of their unique genetic structure at thepopulation level. These results complement the observed high site fidelity of Cobias in SouthCarolina and support a recent study that confirms that Cobia spawn in the inshore aggregations. Ourincreased understanding of Cobia life history will be beneficial for determining the appropriatescale of fishery management for Cobia.16. Dawson, C.E. (1971.) Occurrence and description of prejuvenile and early juvenile Gulf of Mexicocobia, <strong>Rachycentron</strong> <strong>canadum</strong>. Coepeia, 1971(1), 65-71.General morphology and coloration of young cobia, 12.6-55.0 mm SL, are described and illustrated.Prejuveniles were taken in offshore Gulf of Mexico surface nekton collections during June and July.Smallest fish were found 30-40 miles offshore, whereas larger specimens, 45-140 mm SL, havebeen most frequently taken in inshore localities. June collections of prejuveniles suggest late Aprilor May spawning in northern Gulf waters.17. Deng, S., Liu, C., Chen, J., & Ye, G. (2002). The isozyme analysis of different tissue in<strong>Rachycentron</strong> <strong>canadum</strong>. Journal of Zhanjiang Ocean University, 22(6), 1-5.By the vertical polyacrylamide gel electrophoresis, five isozymes (LDH, MDH, ME, POD, EST)from several tissues (brain, heart, muscle, kidney, gonad, liver, blood, spleen, pancreas) of<strong>Rachycentron</strong> <strong>canadum</strong> were studied. The results showed that all isozymes presented tissuespecificity. These specificities were related to their special physiological function. Compared withother teleosts, the isozymic phenotypes of R. <strong>canadum</strong> were much simple with, which may berelated to its generic diversity.18. Denson, M.R., Stuart, K.R., Smith, T.I.J., Weirich, C.R. & Segars, A. (2003). Effects of salinityon growth, survival, and selected hematological parameters of juvenile Cobia <strong>Rachycentron</strong><strong>canadum</strong>. Journal of the World Aquaculture Society, 34(4), 496-504.Cobia <strong>Rachycentron</strong> <strong>canadum</strong> juveniles (119.7 mm TL, weight 8.5 g) were reared for 10 wk atthree salinity levels: 5 ppt, 15 ppt, and 30 ppt. Growth and survival were determined throughbiweekly sampling. Blood samples obtained at termination of the study were analyzed to determinehematocrit, blood osmolality, and total protein. Results indicated that the overall growth of fish wassignificantly affected by salinity. Mean (± SE) total length (TL) and weight of fish reared at asalinity of 30 ppt were 201.7 ± 2.6 mm and 47.6 ± 1.9 g, respectively, followed by fish reared at 15ppt (182.2 ± 1.7 mm, 34.1 ± 1.6 g), and 5 ppt (168.3 ± 5.8 mm TL, 28.3 ± 2.3 g). Differences inspecific growth rates among treatments for the 10-wk period were also significant. No differenceswere detected in mean survival among fish reared at salinities of 5, 15, and 30 ppt (84, 94, and 94%,respectively). However, fish reared at salinity 5 ppt appeared to be in poor health as skin lesions, finerosion, and discoloration were evident. Analysis of blood revealed that, while no differencesexisted among treatments with respect to plasma total protein, fish reared at a salinity of 5 pptexhibited significantly reduced hematocrit (25% vs. > 30%) and plasma osmolality values (318 vs.> 353 mmol/kg) relative to fish reared at higher salinities. Cobia can tolerate exposure to lowsalinity environments for short periods of time without mortality; however, moderate to highsalinities are required for sustained growth and health of this species.19. Deshpande, A., Bhendigeri, S., Shirsekar, T., Dhaware, D. & Khandekar, R.N. (2009).Analysis of heavy metals in marine fish from Mumbai Docks. Environmental Monitoring andAssessment, 159(1-4), 493-500.5
Seafood containing heavy metals as a result of environmental contamination causes toxicity inhuman beings. To evaluate such kind of contamination, our study targeted the analysis of metalssuch as lead, copper, cadmium, mercury, and arsenic in muscle tissue of the fish. The fishcommonly consumed such as Brama brama (Pomfret), <strong>Rachycentron</strong> canadus (Surmai/King Fish),Rastrelliger kanagurta (Mackerel), Eleutheronema tetradactylum (Ravas/Indian salmon), andMetapenaeus monoceros (Brown Prawn) were collected from four different docks in the city. Theheavy metals in tissue samples of fish were estimated using voltammeter and cold vapor atomicabsorption spectrophotometer. Heavy metal concentration in the tissues varied significantlydepending upon the locations from where the fish were collected. Although the concentration ofarsenic, copper, cadmium, and lead were in normal range, the concentration of mercury was foundto exceed the daily permissible levels (1kg/g) as a food source for human consumption. We haveanalyzed heavy metals from different locations in Mumbai-Versova dock, Sassoon dock, NaviMumbai dock, and Mazgaon dock.20. Dhawan, R.M., Namboothiri, P.V.S. & Gopinathan, V.G. (1969). Results of trolling lineoperations in Goa waters during 1965-68. Indian Journal of Fisheries, 16(1-2), 181-187.The results of trolling line operations conducted for the first time in Goa waters by the Directorateof Fisheries, Panaji, during the yrs 1956-68 have been discussed. These operations, in later years,led to starting of a small commercial fishery. The trolling line catches are constituted byScomberomorus commerson, Chorinemus lysan, Caranx sansun, Sphyraena sp, Chirocentrusdorab, <strong>Rachycentron</strong> canadus, Euthynnus affinis and Thynnus macropterus. The size groups,gonadal condition and food of Scomberomorus commerson and Chorinemus lysan which were the 2main spp in the fishery have been described.21. Ditty, J.G. (2001). Preliminary guide to the identification of the early life history stages ofRachycentrid fishes of the Western Central Atlantic. NOAA Technical Memorandum NMFSSEFSC, 460 (12).The family Rachycentridae, contains a single cosmopolitan species, <strong>Rachycentron</strong> <strong>canadum</strong>, foundprimarily in tropical and subtropical waters, except those of the eastern Pacific (Briggs 1960).Cobia are a highly prized recreational species that are also taken incidently in commercial fisheries.In the western Atlantic, cobia fish occurs from Massachusetts to Argentina but are most commonalong the U.S. Atlantic and Gulf coasts. Cobia are usually absent from northern Gulf of Mexico andtemperate Atlantic waters along the U.S. coast during late fall and winter when they are found offthe Florida Keys. Cobia migrates north along the Atlantic and Gulf coasts during spring,reappearing in the northern Gulf during March and April. Cobia is taken off Louisiana and Texasassociated with oil and gas platforms or rafts of Sargassum.22. Ditty, J.G. & Shaw, R.F. (1992). Larval development, distribution, and ecology of cobia<strong>Rachycentron</strong> <strong>canadum</strong> (family: Rachycentridae) in the northern Gulf of Mexico. Fishery Bulleting,90(4), 668-677.Cobia (<strong>Rachycentron</strong> <strong>canadum</strong>) is a highly prized recreational species of worldwide distribution intropical and subtropical seas, but the development, distribution, and ecology of its early life stagesare poorly known. Eggs are spherical, average 1.24 mm in diameter, and have a single oil globule(mean diameter 0.45 mm). The perivitelline space is narrow and the embryo heavily pigmented.Eggs hatch in about 24 h at 29 °C based on the relationship between egg diameter and watertemperature to predict development time in other marine fishes. Larvae hatch at about 2.5 mmSL.Cobia spawns in both estuarine and shelf waters during the day, and eggs and larvae are usuallycollected in the upper meter of the water column. Larvae are recognized by the large supraorbitalridge with a single spine, laterally swollen pterotics, heavy body pigmentation, minute epithelialspicules covering the body integument, and a pair of moderate-to-large, simple spines on either sideof the angle of the posterior preoperculum. Only 70 larvae < 20 mmSL were collected andidentified from the Gulf of Mexico between 1967 and 1988; most occurred between June andSeptember at surface temperatures greater than or equal to 25 °C, salinities > 27 ppt, and within the100 m depth contour. Similar patterns of head spination provide evidence of a sister-grouprelationship between cobia (<strong>Rachycentron</strong> <strong>canadum</strong>) and dolphinfish rather than that previouslyhypothesized between cobia and remoras.23. Dung, L.Q. & Cu, N.D. (2008). Partial chronic toxicity test of copper (Cu), zinc (Zn), and cyanide(Cn) for young cobia fish (<strong>Rachycentron</strong> <strong>canadum</strong>). Marine Research in Indonesia, 33(1), 49-53.6
- Page 1 and 2: COBIA (Rachycentron canadum)A SELEC
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- Page 18 and 19: The spawning season, late June thro
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- Page 28 and 29: 83. George, P.V. & Nadakal, A.M. (1
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- Page 44 and 45: 137. Kaiser, J.B. & Holt, G.J. (200
- Page 46 and 47: (DHA) and vitamin E levels compared
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- Page 50 and 51: growth rates (SGR) did not exceed t
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The techniques of homology cloning
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190. Zhang, H., Mao, L., Feng, J.,
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This suggests that the enrichment o
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formerly characterized elovl5 elong
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208. Weirich, C.R., Stokes, A.D., S
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trypsin activities of intestine of
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decreased gradually as fish body we
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BIA methodology can be utilized as
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cobia were 21.72 mg kg -1 , 22.38 m
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effects upon final product quality,
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than the optimal requirement of cob
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A 9-week feeding trial was conducte
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soybean meal in Cobia, Rachycentron
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261. Sun, L., Chen, H., Huang, L.,
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fishes and invertebrates. Here we i
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274. Watson, A.M., Buentello, A. &
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estimated to be 44.7 mg kg -1 based
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20% of alternative protein meal, ne
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levels of methionine (0.61%, 0.83%,
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298. Mach, D.T.N. & Nortvedt, R. (2
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acids (FFA), peroxide value (PV), t
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068Breitenbach, B.078Brenkert, K.01
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271Duncan, M.226Dung, L.Q.023DuPaul
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139, 149Kilduff, P.180Kim, I.H.088K
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265Myrseth, B.140Nabavi, S.M.B.001,
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244Shi, C.071Shi, G.218, 262, 287Sh
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291Xie, J.269, 270Xu, H.037, 190Xu,