Effects of dietary Iranian acorn on the growth performance, feed utilization and carcass composition of common carp

Document Type : scientific research article

Authors

1 Corresponding Author, Assistant Prof., Dept. of Fisheries, Faculty of Natural Resources, Behbahan Khatam Alanbia University of Technology, Behbahan, Iran

2 Bachelor, Dept. of Fisheries, Faculty of Natural Resources, Behbahan Khatam Alanbia University of Technology, Behbahan, Iran

Abstract

Oak acorn is widely used as animal feed due to its low price. Oak acorns (Quercus brantii) were processed by de-hulling, drying and milling. In acorn flour, the total phenolic compounds, non-tannin phenols and condensed tannins were 14.71, 0.35 and 6.60 g/100g on the basis of dry matter respectively. Five isonitrogenous and isoenergetic diets with different levels of acorn at 0 (control), 25, 50, 75 and 100 g/kg, were prepared. A total of 435 fish (average weight 0.3 g) were randomly distributed in 15 tanks with three replicates and fed for 10 weeks. Polynomial orthogonal contrast analysis revealed that there were no significant differences in terms of feed intake, feed conversion ratio, protein retention, carcass ash and survival rate between treatments (p>0.05). Dietary intake of acorn significantly affected the weight after four weeks, final weight after 10 weeks, total length, head depth, specific growth rate, condition factor, protein efficiency ratio, lipid retention and carcass lipid and moisture contents, which represented linear order polynomial (LOP) models, but crude protein content of carcass displayed a cubic order polynomial (COP) model, using optimal acorn flour levels of 25.00 – 64.28 g/kg. Acorn flour improved the protein level of carcass, but deteriorated the growth performance and carcass lipid and moisture levels. Therefore, even if the amount of de-hulled acorn flour in the diet is low (2.5 % of diet), it is not allowed to use it without further processing.

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1.Tacon, A. G. J., & Metian, M. (2015). Feed matters: satisfying the feed demand of aquaculture. Reviews in Fisheries Science and Aquaculture. 23, 1-10.
2.Ozcan, T. (2006). Total protein and amino acid compositions in the acorns of Turkish Quercus L. taxa. Genetic Resources and Crop Evolution. 53, 419-29.
3.Tejerina, D., Garcia-Torres, S., Vaca,
M. C., Vasquez, F. M., & Cava, R. (2011). Acorns (Quercus rotundifolia Lam.) and grass as natural sources of antioxidants and fatty acids in the “montanera” feeding of Iberian pig: intra- and inter-annual variations. Food Chemistry. 124, 997-1004.
4.Vinha, A. F., Barreira, J. C. M., Costa, A. S. G., & Oliveira, M. B. P. P. (2016). A new age for Quercus spp. fruits: review on nutritional and phytochemical composition and related biological activities of acorns. Comprehensive Reviews in Food Science and Food Safety. 15, 947-981.
5.Frutos, P., Hervas, G., Giraldez, F. J., & Mantecon, A. R. (2004). Review. Tannins and ruminant nutrition. Spanish Journal of Agricultural Research, 2, 191-202.
6.Omnes, M. H., Goasduff, J. L., Delliou, H. L., Bayon, N. L., Quazuguel, P., & Robin, J. H. (2017). Effects of dietary tannin on growth, feed utilization and digestibility, and carcass composition in juvenile European seabass (Dicentrarchus labrax L.). Aquaculture Reports. 6, 21-27.
7.Talebian Nik, S. S., & Alamdari, H. (2020). Adding Iranian oak acorn (Quercus brantii) to the diet of common carp (Cyprinus carpio Linnaeus, 1758) and its effects on growth performance, carcass composition and resistance to salinity stress. Iranian Scientific Fisheries Journal. 29 (2), 83-91.
8.Watanabe, W. O., Ellis, S. C., & Chaves, J. (2001). Effects of dietary lipid and energy to protein ratio on growth and feed utilization of juvenile mutton snapper Lutjanus analis fed isonitrogenous diets at two temperatures. Journal of the World Aquaculture Society. 32 (1), 30-40.
9.Torrecillas, S., Montero, D., Carvalho, M., Benitez-Santana, T., & Izquierdo, M. (2021). Replacement of fish meal by Antarctic krill meal in diets for European sea bass Dicentrarchus labrax: Growth performance, feed utilization and liver lipid metabolism. Aquaculture, 545, 737166.
10.Mazurkiewicz, J. (2009). Utilization of domestic plant components in diets for common carp Cyprinus carpio L. Archives of Polish Fisheries, 17, 5-39.
11.AOAC (Association of Official Analytical Chemists). (2000). Official Methods of Analysis 17th ed. Washington D.C., 2200 p.
12.Thiex, N., & Novotny, L. (2012). Determination of ash in animal feed: AOAC official method 942.05 revisited. Journal of AOAC international, 95 (5), 1392-1397.
13.Makkar, H. P. S. (2003). Quantification of tannins in tree foliage: A laboratory manual. FAO/IAEA.
14.NRC (National Research Council). (2011). Nutrient requirements of fish and shrimp. National Academy Press. Washington, D.C., 376 p.
15.Keshavarzi, S., Houshmand, M., & Bahreini Behzadi, M. R. (2017). Age-specific response of broilers to dietary inclusion of a high-tannin feedstuff. Poultry Science Journal. 5 (2), 83-90.
16.Huang, Q., Liu, X., Zhao, G., Hu, T., & Wang, Y. (2018). Potential and challenges of tannins as an alternative to in-feed antibiotics for farm animal production. Animal Nutrition. 4, 137-150.
17.Becker, K., & Makkar, H. P. S. (1999). Effects of dietary tannic acid and quebracho tannin on growth performance and metabolic rates of common carp (Cyprinus carpio L.). Aquaculture, 175, 327-335.
18.Jackson, A. J., Capper, B. S., & Matty, A. J. (1982). Evaluation of some plant protein in complete diets for the tilapia Sarotherodon mossambicus. Aquaculture. 27 (2), 97-109.
19.Mukhopadhyay, N., & Ray, A. K. (1999). Utilization of copra meal in the formulation of compound diets for rohu, Labeo rohita, fingerlings. Journal of Applied Ichthyology. 15, 127-131.
20.Collins, S. A., Mansfield, G. S., Desai, A. R., Van Kessel, A. G., Hill, J. E., & Drew, M. D. (2013). Structural equation modeling of antinutrients in rainbow trout diets and their impact on feed intake and growth. Aquaculture, 416, 219-227.
21.Hossain, M. A., & Jauncey, K. (1989). Nutritional evaluation of some Bangladeshi oilseed meals as partial substitutes for fish meal in the diet of common carp, Cyprinus carpio L. Aquaculture Research, 20, 255-268.
22.Mwachireya, S. A., Beames, R. M., Higgs, D. A., & Dosanjh, B. S. (1999). Digestibility of canola protein products derived from the physical, enzymatic and chemical processing of commercial canola meal in rainbow trout Oncorhynchus mykiss (Walbaum) held in fresh water. Aquacult Nutrition. 5, 73-82.
23.Gaber, M. M. (2006). Partial and complete replacement of fish meal by broad bean meal in feeds for Nile tilapia, Oreochromis niloticus, L., fry. Aquaculture Research, 37, 986-993.
24.Horstmann, S. W., Lynch, K. M., & Arendt, E. K. (2017). Starch characteristics linked to gluten-free products. Foods,
6 (29), 1-21.
25.Stevenson, D. G., Jane, J. L., & Inglett, G. E. (2006). Physicochemical properties of pin oak (Quercus palustris Muenchh.) acorn starch. Starch/Staerke 58, 553-560.
26.Cappai, M. G., Wolf, P., Pinna, W., & Kamphues, J. (2013). Pigs use endogenous proline to cope with acorn (Quercus pubescens Willd.) combined diets high in hydrolysable tannins. Livestock Science, 155, 316-322.
27.Hossain, M. A., Focken, U., & Becker, K. (2001). Evaluation of an unconventional legume seed, Sesbania aculeata, as a dietary protein source for common carp (Cyprinus carpio L.). Aquaculture, 198, 129-140.
28.Fauconneau, B., Alami-Duranteb, H., Larochec, M., Marceld, J., & Vallot, D. (1995). Growth and meat quality relations in carp. Aquaculture, 129, 265-297.
29.Narui, M., & Alamdari, H. (2022). Effect of feeding with soaked and fermented Iranian acorn (Quercus brantii) on the growth, feed utilization and carcass composition of common carp (Cyprinus carpio). Iranian Scientific Fisheries Journal. 31 (1), 47-56.
30.Smith, S., Naylor, R. J., Knowles, E. J., Mair, T. S., Cahalan, S. D., Fews, D., & Dunkel, B. (2015). Suspected
acorn toxicity in nine horses. Equine Veterinary Journal. 47, 568-72.