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Estimation of dietary copper requirements of juvenile tilapia, Oreochromis niloticus 5 O. aureus

Published online by Cambridge University Press:  18 August 2016

S.Y. Shiau*
Affiliation:
Department of Food Science, National Taiwan Ocean University, Keelung 202, Taiwan
Y.C. Ning
Affiliation:
Department of Food Science, National Taiwan Ocean University, Keelung 202, Taiwan
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Abstract

An 8-week feeding trial was conducted to determine the dietary copper (Cu) requirement of juvenile hybrid tilapia, Oreochromis niloticus 5 O. aureus. Purified diets with eight levels (0, 1, 2, 3, 4, 8, 12 or 20 mg Cu per kg diet) of supplemental Cu were given to tilapia (mean initial weight 0·79±0·03 g). Each diet was given to three replicate groups of fish. The rearing water contained 0·98 µg Cu per l. Weight gain was highest in fish given diets supplemented with 2 mg Cu per kg diet, followed by the group given 1 mg Cu per kg diet, then the unsupplemented control group, and was lowest in the 20 mg Cu per kg diet group. The differences between each of these four groups were significant (P < 0·05). Food efficiency (FE) of fish showed a similar trend to that of weight gain. Blood haemoglobin (Hb) and haematocrit (Hct) concentrations were lowest in fish given ≥ 12 mg Cu per kg diet, followed by fish given the unsupplemented control diet and highest in fish given 2 mg Cu per kg diet (Hb) and 2 and 3 mg Cu per kg diet (Hct). Plasma ceruloplasmin activity was higher in fish given 1 and 2 mg Cu per kg diet, followed by 3 to 12 mg Cu per kg diet and the control group, and lowest in fish given 20 mg Cu per kg diet. The body Cu content in fish generally increased as the dietary Cu supplementation level increased. Analysis by broken-line regression of weight gain percent and by linear regression of the whole-body Cu retention of fish indicated that the adequate dietary Cu concentration in growing tilapia is about 4 mg Cu per kg diet.

Type
Non-ruminant nutrition, behaviour and production
Copyright
Copyright © British Society of Animal Science 2003

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References

Agrawal, N. K. and Mahajan, C. L. 1983. Haematological and haematopoietic studies in pyridoxine-deficient fish, Channa punctatus Bloch. Journal of Fish Biology 22: 91103.Google Scholar
Allen, C. B. 1996. Effects of dietary copper deficiency on relative food intake and growth efficiency in rats. Physiology and Behavior 59: 247253.CrossRefGoogle ScholarPubMed
Association of Official Analytical Chemists. 1995. Official methods of analysis, 16th edition. AOAC, Arlington, VA.Google Scholar
Davis, G. K. and Mertz, W. 1986. Copper. In Trace elements in human and animal nutrition, fifth edition, volume 1 (ed. Mertz, W.), pp. 301464. Academic Press, San Diego, CA.Google Scholar
El-Sayed, A.-F.M. 1999. Alternative dietary protein sources for farmed tilapia, Oreochromis spp. Aquaculture 179: 149168.CrossRefGoogle Scholar
Gatlin, D. M. and Wilson, R. P. 1986. Dietary copper requirement of fingerling channel catfish. Aquaculture 54: 277285.CrossRefGoogle Scholar
Goldberg, A., Williams, C. B., Jones, R. S., Yanagita, M., Cartwright, G. E. and Wintrobe, M. M. 1956. Studies on copper metabolism. XXII. Hemolytic anemia in chickens induced by the administration of copper. The Journal of Laboratory and Clinical Medicine 48: 442453.Google Scholar
Knox, D., Cowey, C. B. and Adron, J. W. 1982. Effects of dietary copper and copper: zinc ratio on rainbow trout Salmo gairdneri . Aquaculture 27: 111119.Google Scholar
Knox, D., Cowey, C. B. and Adron, J. W. 1984. Effects of dietary zinc intake upon copper metabolism in rainbow trout (Salmo gairdneri). Aquaculture 40: 199207.CrossRefGoogle Scholar
Lanno, R. P., Slinger, S. J. and Hilton, J. W. 1985. Effect of ascorbic acid on dietary copper in rainbow trout (Salmo gairdneri Richardson). Aquaculture 49: 269287.Google Scholar
Louro, M. O., Cocho, J. A. and Tutor, J. C. 2001. Assessment of copper status in pregnancy by means of determining the specific oxidase activity of ceruloplasmin. Clinica Chimica Acta 312: 123127.Google Scholar
Murai, T., Andrews, J. W. and Smith, R.G. Jr 1981. Effects of dietary copper on channel catfish. Aquaculture 22: 353357.CrossRefGoogle Scholar
O’Dell, B.L. 1976a. Biochemistry and physiology of copper in vertebrates. In Trace elements in human health and disease, volume 1 (ed. Prasad, A. S.), pp. 391413. Academic Press, New York, NY.Google Scholar
O’Dell, B.L. 1976b. Biochemistry of copper. Symposium on trace elements. The Medical Clinics of North America 60: 697703.Google Scholar
Ogino, C. and Yang, G. Y. 1980. Requirement of carp and rainbow trout for dietary manganese and copper. Nippon Suisan Gakkaishi 46: 455458.Google Scholar
Robbins, K. R. 1986. A method, SAS program, and example for fitting the broken line to growth data. University of Tennesse Agricultural Experiment Station research report, University of Tennesse, Knoxville, TN.Google Scholar
Schosinsky, K. H., Lehmann, H. P. and Beeler, M. F. 1974. Measurement of ceruloplasmin from its oxidase activity in serum by use of o-dianisidine dihydrochloride. Clinical Chemistry 20: 15561563.Google Scholar
Shiau, S. Y. and Chin, Y. H. 1999. Estimation of the dietary biotin requirement of juvenile hybrid tilapia, Oreochromis niloticus 5 O. aureus. Aquaculture 170: 7178.Google Scholar
Shiau, S. Y. and Hsieh, J. F. 2001. Quantifying the dietary potassium requirement of juvenile hybrid tilapia, Oreochromis niloticus 5 O. aureus. British Journal of Nutrition 85: 213218.Google Scholar
Shiau, S. Y. and Liang, H. S. 1995. Carbohydrate utilization and digestibility by tilapia, Oreochromis niloticus 5 O. aureus, are affected by chromic oxide inclusion in the diet. Journal of Nutrition 125: 976982.Google ScholarPubMed
Shiau, S. Y. and Lo, P. S. 2000. Dietary choline requirements of juvenile hybrid tilapia, Oreochromis niloticus 5 O. aureus. Journal of Nutrition 130: 100103.Google Scholar
Shiau, S. Y. and Shiau, L. F. 2001. Re-evaluation of the vitamin E requirements of juvenile tilapia (Oreochromis niloticus 5 O. aureus). Animal Science 72: 529534.Google Scholar
Shiau, S. Y. and Shy, S. M. 1998. Dietary chromic oxide inclusion level required to maximize glucose utilization in hybrid tilapia, Oreochromis niloticus 5 O. aureus. Aquaculture 161: 357364.CrossRefGoogle Scholar
Statistical Analysis Systems Institute. 1994. SAS user’s guide. Statistics version 611 edition. SAS Institute, Cary, NC.Google Scholar
Wilson, R. P. and El Naggar, G. 1992. Potassium requirement of fingerling channel catfish, Ictalurus punctatus. Aquaculture 108: 169175.CrossRefGoogle Scholar