Effects of dietary oak (Quercus aegilops L.) acorn on growth performance, somatic indices, and hemato-biochemical responses of common carp, Cyprinus carpio L., at different stocking densities

References

• Abdel-Latif, H. M. R., M. Abdel-Tawwab, A. Khafaga, and M. A. O. Dawood. 2020. Dietary oregano essential oil improved the growth performance via enhancing the intestinal morphometry and hepato-renal functions of common carp (Cyprinus carpio L.) fingerlings. Aquaculture 526:735432. doi:10.1016/j.aquaculture.2020.735432.
   Web of Science ®Google Scholar
• Abdel-Tawwab, M. 2012. Effects of dietary protein levels and rearing density on growth performance and stress response of Nile tilapia, Oreochromis niloticus (L.). International Aquatic Research 4 (1):1–13. doi:10.1186/2008-6970-4-3.
   Google Scholar
• Abdel-Tawwab, M. 2016. Effect of feed availability on susceptibility of Nile tilapia, Oreochromis niloticus (L.) to environmental zinc toxicity: Growth performance, biochemical response, and zinc bioaccumulation. Aquaculture 464:309–15. doi:10.1016/j.aquaculture.2016.07.009.
   Web of Science ®Google Scholar
• Abdel-Tawwab, M., N. M. Abdulrahman, A. I. Baiz, P. J. Nader, and I. H. A. Al-Refaiee. 2020. The using of Chlorella pyrenoidosa and Daphnia magna as feed supplements for common carp, Cyprinus carpio: Growth performance, somatic indices, and hemato-biochemical biomarkers. Journal of Applied Aquaculture 1–15. doi:10.1080/10454438.2020.1787291.
   Google Scholar
• Abdel-Tawwab, M., I. Adeshina, A. Jenyo-Oni, E. K. Ajani, and B. O. Emikpe. 2018. Growth, physiological, antioxidants, and immune response of African catfish, Clarias gariepinus (B.), to dietary clove basil, Ocimum gratissimum, leaf extract and its susceptibility to Listeria monocytogenes infection. Fish & Shellfish Immunology 78:346–54. doi:10.1016/j.fsi.2018.04.057.
   PubMed Web of Science ®Google Scholar
• Abdel-Tawwab, M., and D. A. El-Araby. 2021. Immune and antioxidative effects of dietary licorice (Glycyrrhiza glabra L.) on performance of Nile tilapia, Oreochromis niloticus (L.) and its susceptibility to Aeromonas hydrophila infection. Aquaculture 530:735828. doi:10.1016/j.aquaculture.2020.735828.
   Web of Science ®Google Scholar
• Abdel-Tawwab, M., A. E. Hagras, M. Heba Allah, M. N. Elbaghdady, and Monier. 2014. Dissolved oxygen level and stocking density effects on growth, feed utilization and physiology of juvenile Nile Tilapia, Oreochromis niloticus. Journal of Applied Aquaculture 26 (4):340–55. doi:10.1080/10454438.2014.959830.
   Google Scholar
• Abdel-Tawwab, M., and H. S. Hamed. 2020. Antagonistic effects of dietary guava (Psidium guajava) leaves extract on growth, hemato-biochemical, and immunity response of cypermethrin-intoxicated Nile tilapia, Oreochromis niloticus, fingerlings. Aquaculture 529:735668. doi:10.1016/j.aquaculture.2020.735668.
   Web of Science ®Google Scholar
• Adeshina, I., M. Abdel-Tawwab, Z. A. Tijjani, L. O. Tiamiyu, and A. Jahanbakhshi. 2021. Dietary Tridax procumbens leaves extract stimulated growth, antioxidants, immunity, and resistance of Nile tilapia, Oreochromis niloticus, to monogenean parasitic infection. Aquaculture 532:736047. doi:10.1016/j.aquaculture.2020.736047.
   Web of Science ®Google Scholar
• Adeshina, I., A. Jenyo‐Oni, B. O. Emikpe, E. K. Ajani, and M. Abdel‐Tawwab. 2019. Stimulatory effect of dietary clove, Eugenia caryophyllata, bud extract on growth performance, nutrient utilization, antioxidant capacity, and tolerance of African catfish, Clarias gariepinus (B.), to Aeromonas hydrophila infection. Journal of the World Aquaculture Society 50 (2):390–405. doi:10.1111/jwas.12565.
   Web of Science ®Google Scholar
• Adineh, H., M. Naderi, M. K. Hamidi, and M. Harsij. 2019. Biofloc technology improves growth, innate immune responses, oxidative status, and resistance to acute stress in common carp (Cyprinus carpio) under high stocking density. Fish & Shellfish Immunology 95:440–48. doi:10.1016/j.fsi.2019.10.057.
   PubMed Web of Science ®Google Scholar
• Ahmadifar, E., M. Yousefi, M. Karimi, R. F. Raieni, M. Dadar, S. Yilmaz, M. A. O. Dawood, and H. M. R. Abdel-Latif. 2021. Benefits of dietary polyphenols and polyphenol-rich additives to aquatic animal health: An overview. Reviews in Fisheries Science & Aquaculture. doi:10.1080/23308249.2020.1818689.
   Web of Science ®Google Scholar
• Al-Jassim, R., K. Ereifej, R. Shibli, and A. Abudabos. 1988. Utilization of concentrated diets containing acorns (Quercus aegilops and Quercus coccifera) and urea by growing Awassi lambs. Small Ruminant Research 29 (3):289–93. doi:10.1016/S0921-4488(97)00124-7.
   Google Scholar
• Andrew, J. E., J. Holm, S. Kadri, and F. A. Huntingford. 2004. The effect of competition on the feeding efficiency and feed handling behaviour in gilthead sea bream (Sparus aurata L.) held in tanks. Aquaculture 232 (1–4):317–31. doi:10.1016/S0044-8486(03)00528-3.
   Web of Science ®Google Scholar
• Babalola, T. O. O., M. A. Adebayo, D. F. Apata, and J. S. Omotosho. 2009. Effect of dietary alternative lipid sources on haematological parameters and serum constituents of Heterobranchus longifilis fingerlings. Tropical Animal Health and Production 41 (3):371–77. doi:10.1007/s11250-008-9199-1.
   PubMed Web of Science ®Google Scholar
• Barton, B. A. 2002. Stress in fishes: A diversity of responses with particular reference to changes in circulating corticosteroids. Integrative and Comparative Biology 42 (3):517–25. doi:10.1093/icb/42.3.517.
   PubMed Web of Science ®Google Scholar
• Bavčević, L., T. Klanjšček, V. Karamarko, I. Aničić, and T. Legović. 2010. Compensatory growth in gilthead sea bream (Sparus aurata) compensates weight, but not length. Aquaculture 301 (1–4):57–63. doi:10.1016/j.aquaculture.2010.01.009.
   Web of Science ®Google Scholar
• Bohlouli, S., G. Ghaedi, M. Heydari, A. Rahmani, and E. Sadeghi. 2016. Effects of dietary Persian oak (Quercus brantii var. persica) fruit extract on survival, growth performance, haematological and immunological parameters in rainbow trout, Oncorhynchus mykiss, fingerlings. Aquaculture Nutrition 22 (4):745–51. doi:10.1111/anu.12290.
   Web of Science ®Google Scholar
• Bolasina, S., M. Tagawa, and Y. Yamashita. 2006. Effect of stocking density on growth, digestive enzyme activity and cortisol level in larvae and juveniles of Japanese flounder, Paralichthys olivaceus. Aquaculture 259 (1–4):432–43. doi:10.1016/j.aquaculture.2006.05.021.
   Web of Science ®Google Scholar
• Boyd, C. E., and C. S. Tucker. 2012. Pond aquaculture water quality management. Boston, MA: Kluwer Academic Publishers.
   Google Scholar
• Brown, B. A. 1988. Routine hematology procedures. In Hematology, principles and procedures, ed. B. A. Brown, 7–122. Philadelphia, PA: Leo and Fabiger.
   Google Scholar
• Burgos-Aceves, M. A., L. Lionetti, and C. Faggio. 2019. Multidisciplinary haematology as prognostic device in environmental and xenobiotic stress-induced response in fish. The Science of the Total Environment 670:1170–83.
   PubMed Web of Science ®Google Scholar
• Burlacu, E., A. Nisca, and C. Tanase. 2020. A comprehensive review of phytochemistry and biological activities of Quercus species. Forests 11 (9):904. doi:10.3390/f11090904.
   Web of Science ®Google Scholar
• Cantos, Espín, López-Bote, de la Hoz, et al.,  (2003). Phenolic Compounds and fatty acids from acorns (Quercus spp.), the main dietary constituent of free-ranged iberian pigs. Journal of Agricultural and Food Chemistry, 51(21):6248–55. doi:10.1021/jf030216v.
   PubMed Web of Science ®Google Scholar
• Chakraborty, S. B., and C. Hancz. 2011. Application of phytochemicals as immunostimulant, antipathogenic and antistress agents in finfish culture. Reviews in Aquaculture 3 (3):103–19. doi:10.1111/j.1753-5131.2011.01048.x.
   Web of Science ®Google Scholar
• Chakraborty, S. B., P. Horn, and C. Hancz. 2014. Application of phytochemicals as growth‐promoters and endocrine modulators in fish culture. Reviews in Aquaculture 6 (1):1–19. doi:10.1111/raq.12021.
   Web of Science ®Google Scholar
• Cheynier, V. 2012. Phenolic compounds: From plants to foods. Phytochemistry Reviews 11:153–77.
   Web of Science ®Google Scholar
• Davis, A. K., D. L. Maney, and J. C. Maerz. 2008. The use of leukocyte profiles to measure stress in vertebrates: A review for ecologists. Functional Ecology 22 (5):760–72. doi:10.1111/j.1365-2435.2008.01467.x.
   Web of Science ®Google Scholar
• Dytham, C. 2011. Choosing and using statistics: A biologist’s guide. London: Blackwell Science Ltd.
   Google Scholar
• Engström, M. 2016. Understanding the bioactivity of plant tannins: Developments in analysis methods and structure-activity studies. Turku, Finland: Painosalama Oy.
   Google Scholar
• Fazelan, Z., Y. A. Vatnikov, E. V. Kulikov, V. G. Plushikov, and M. Yousefi. 2020. Effects of dietary ginger (Zingiber officinale) administration on growth performance and stress, immunological, and antioxidant responses of common carp (Cyprinus carpio) reared under high stocking density. Aquaculture 518:734833. doi:10.1016/j.aquaculture.2019.734833.
   Web of Science ®Google Scholar
• Ferreira, V. C. S., D. Morcuende, S. H. Hérnandez-López, M. S. Madruga, F. A. P. Silva, and M. J. Estévez. 2017. Antioxidant extracts from acorns (Quercus ilex L.) effectively protect ready-to-eat (RTE) chicken patties irrespective of packaging atmosphere. Journal of Food Science 82 (3):622–31. doi:10.1111/1750-3841.13640.
   PubMed Web of Science ®Google Scholar
• Firouzbakhsh, F. F., M. Noori, K. Khalesi, and K. Jani-Khalili. 2011. Effects of a probiotic, protexin, on the growth performance and hematological parameters in the Oscar (Astronotus ocellatus) fingerlings. Fish Physiology and Biochemistry 37 (4):833–42. doi:10.1007/s10695-011-9481-4.
   PubMed Web of Science ®Google Scholar
• Harikrishnan, R., M. Nisha Rani, and C. Balasundaram. 2003. Hematological and biochemical parameters in common carp, Cyprinus carpio, following herbal treatment for Aeromonas hydrophila infection. Aquaculture 221 (1–4):41–50. doi:10.1016/S0044-8486(03)00023-1.
   Web of Science ®Google Scholar
• Hoseini, S. M., M. Yousefi, S. H. Hoseinifar, and H. Van Doan. 2019. Effects of dietary arginine supplementation on growth, biochemical, and immunological responses of common carp (Cyprinus carpio L.), stressed by stocking density. Aquaculture 503:452–59. doi:10.1016/j.aquaculture.2019.01.031.
   Web of Science ®Google Scholar
• Irianto, A., and B. Austin. 2002. Use of probiotic to control furunclosis in rainbow trout. Journal of Fish Diseases 25 (6):333–42. doi:10.1046/j.1365-2761.2002.00375.x.
   Web of Science ®Google Scholar
• Jerez-Cepa, I., A. Marín-Rincón, G. Martínez-Rodríguez, I. Ruiz-Jarabo, and J. M. Mancera. 2020. A natural additive in the diet to improve growth and reduce energy expenditure of gilthead seabream (Sparus aurata L.): Attenuation of high stocking density stress responses. Aquaculture 524:735263. doi:10.1016/j.aquaculture.2020.735263.
   Web of Science ®Google Scholar
• Khan, M., K. Shahzad, A. Chatta, M. Sohail, M. Piria, and T. Treer. 2016. A review of introduction of common carp Cyprinus carpio in Pakistan: Origin, purpose, impact and management. Croatian Journal of Fisheries 74 (2):71–80. doi:10.1515/cjf-2016-0016.
   Google Scholar
• Khwarahm, N. R. 2020. Mapping current and potential future distributions of the oak tree (Quercus aegilops) in the Kurdistan Region, Iraq. Ecological Processes 9 (1):56. doi:10.1186/s13717-020-00259-0.
   Web of Science ®Google Scholar
• Kpundeh, M. D., P. Xu, H. Yang, J. Qiang, and J. He. 2013. Stocking densities and chronic zero culture water exchange stress effects on biological performances, hematological and serum biochemical indices of GIFT Tilapia juveniles (Oreochromis niloticus). Journal of Aquaculture Research & Development 4 (5):1–5. doi:10.4172/2155-9546.1000189.
   Google Scholar
• Li, D., Z. Liu, and C. Xie. 2012. Effect of stocking density on growth and serum concentrations of thyroid hormones and cortisol in Amur sturgeon, Acipenser schrenckii. Fish Physiology and Biochemistry 38 (2):511–20. doi:10.1007/s10695-011-9531-y.
   PubMed Web of Science ®Google Scholar
• Lupatsch, I., G. A. Santos, J. W. Schrama, and J. A. J. Verreth. 2010. Effect of stocking density and feeding level on energy expenditure and stress responsiveness in European sea bass Dicentrarchus labrax. Aquaculture 298 (3–4):245–50. doi:10.1016/j.aquaculture.2009.11.007.
   Web of Science ®Google Scholar
• Mahmoud, H. K., F. M. Reda, M. Alagawany, and M. R. Farag. 2021. Ameliorating deleterious effects of high stocking density on Oreochromis niloticus using natural and biological feed additives. Aquaculture 531:735900. doi:10.1016/j.aquaculture.2020.735900.
   Web of Science ®Google Scholar
• Menezes, C., I. Ruiz-Jarabo, J. A. Martos-Sitcha, C. Toni, J. Salbego, A. Becker, V. L. Loro, G. Martínez-Rodríguez, J. M. Mancera, and B. Baldisserotto. 2015. The influence of stocking density and food deprivation in silver catfish (Rhamdia quelen): A metabolic and endocrine approach. Aquaculture 435:257–64. doi:10.1016/j.aquaculture.2014.09.044.
   Web of Science ®Google Scholar
• Mommsen, T. P. 2001. Paradigms of growth in fish. Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology 129 (2–3):207–19. doi:10.1016/S1096-4959(01)00312-8.
   PubMed Web of Science ®Google Scholar
• Papoti, V. T., N. Kizaki, A. Skaltsi, P. D. Karayannakidis, and M. Papageorgiou. 2018. The phytochemical rich potential of acorn (Quercus aegilops) products and by products. Food Science and Biotechnology 27 (3):819–28. doi:10.1007/s10068-017-0293-x.
   PubMed Web of Science ®Google Scholar
• Paray, B. A., S. M. Hoseini, S. H. Hoseinifar, and H. Van Doan. 2020. Effects of dietary oak (Quercus castaneifolia) leaf extract on growth, antioxidant, and immune characteristics and responses to crowding stress in common carp (Cyprinus carpio). Aquaculture 524:735276. doi:10.1016/j.aquaculture.2020.735276.
   Web of Science ®Google Scholar
• Polakof, S., F. J. Arjona, S. Sangiao-Alvarellos, M. P. Martín Del Río, J. M. Mancera, and J. L. Soengas. 2006. Food deprivation alters osmoregulatory and metabolic responses to salinity acclimation in gilthead sea bream Sparus auratus. Journal of Comparative Physiology B 176 (5):441–52. doi:10.1007/s00360-006-0065-z.
   PubMed Web of Science ®Google Scholar
• Rahman, M. M., and C. G. Meyer. 2009. Effects of food type on diel behaviours of common carp Cyprinus carpio in simulated aquaculture pond conditions. Journal of Fish Biology 74 (10):2269–78. doi:10.1111/j.1095-8649.2009.02236.x.
   PubMed Web of Science ®Google Scholar
• Ran, Huang, Hu, Tacon, He, et al.,  2016. Effects of dietary live and heat-inactive baker’s yeast on growth, gut health, and disease resistance of Nile tilapia under high rearing density. Fish & Shellfish Immunology 56:263–71. doi:10.1016/j.fsi.2016.07.001.
   PubMed Web of Science ®Google Scholar
• Rashidian, G., S. B. Gorji, M. N. Farsani, M. D. Prokić, and C. Faggio. 2020. The oak (Quercus brantii) acorn as a growth promotor for rainbow trout (Oncorhynchus mykiss): Growth performance, body composition, liver enzymes activity and blood biochemical parameters. Natural Product Research 34 (17):2413–23. doi:10.1080/14786419.2018.1538994.
   PubMed Web of Science ®Google Scholar
• Rebl, A., M. Zebunke, A. Borchel, R. Bochert, M. Verleih, and T. Goldammer. 2017. Microarray-predicted marker genes and molecular pathways indicating crowding stress in rainbow trout (Oncorhynchus mykiss). Aquaculture 473:355–65. doi:10.1016/j.aquaculture.2017.03.003.
   Web of Science ®Google Scholar
• Ruane, N. M., E. C. Carballo, and J. Komen. 2002. Increased stocking density influences the acute physiological stress response of common carp Cyprinus carpio (L.). Aquaculture Research 33 (10):777–84. doi:10.1046/j.1365-2109.2002.00717.x.
   Web of Science ®Google Scholar
• Sadoul, B., and M. M. Vijayan. 2016. Stress and growth. In Fish physiology: Biology of stress in fish, ed. C. B. Schreck, L. Tort, A. P. Farrell, and C. J. Brauner, 167–205. Elsevier Science Publishing Co. Inc., San Diego, USA.
   Google Scholar
• Soleimanzadeh, A., M. Kian, S. Moradi, and F. Malekifard. 2018. Protective effects of hydro-alcoholic extract of Quercus brantii against lead-induced oxidative stress in the reproductive system of male mice. Avicenna Journal of Phytomedicine 8 (5):448–56.
   PubMed Web of Science ®Google Scholar
• Van Doan, H., S. H. Hoseinifar, K. Sringarm, S. Jaturasitha, B. Yuangsoi, M. A. O. Dawood, M. Á. Esteban, E. Ringø, and C. Faggio. 2019. Effects of Assam tea extract on growth, skin mucus, serum immunity and disease resistance of Nile tilapia (Oreochromis niloticus) against Streptococcus agalactiae. Fish Shellfih Immunol 93:428–35.
   PubMed Web of Science ®Google Scholar
• Van Kampen, E. J., and W. G. Zijlstra. 1961. Standardization of hemoglobinometry II. The hemiglobincyanide method. Clinica Chimica Acta 6 (4):538–44. doi:10.1016/0009-8981(61)90145-0.
   PubMed Web of Science ®Google Scholar
• Vilizzi, L., and A. S. Tarkan. 2015. Experimental evidence for the effects of common carp (Cyprinus carpio L., 1758) on freshwater ecosystems. LIMNOFISH- Journal of Limnology and Freshwater Fisheries Research 26 (3):340–55. doi:10.17216/LimnoFish-5000130907.
   Google Scholar
• Vinha, A., J. Barreira, I. Ferreira, and M. Oliveira. 2020. Therapeutic, phytochemistry, and pharmacology of acorns (Quercus nuts): A review. In Murthy, H.N. and V.A. Bapat, eds., Bioactive compounds in underutilized fruits and nuts, 1–15. Cham, Switzerland: Springer.
   Google Scholar
• Yousefi, M., S. M. Hoseini, Y. A. Vatnikov, E. V. Kulikov, and S. G. Drukovsky. 2019. Rosemary leaf powder improved growth performance, immune and antioxidant parameters, and crowding stress responses in common carp (Cyprinus carpio) fingerlings. Aquaculture 505 (2019):473–80. doi:10.1016/j.aquaculture.2019.02.070.
   Google Scholar
• Yousefi, M., S. V. Shabunin, Y. A. Vatnikov, E. V. Kulikov, H. Adineh, M. K. Hamidi, and S. M. Hoseini. 2020. Effects of lavender (Lavandula angustifolia) extract inclusion in diet on growth performance, innate immunity, immune-related gene expression, and stress response of common carp, Cyprinus carpio. Aquaculture 515:734588. doi:10.1016/j.aquaculture.2019.734588.
   Web of Science ®Google Scholar
• Zaki, M. A. A., A. N. Alabssawy, A. M. Nour, M. F. El Basuini, M. A. O. Dawood, S. Alkahtani, and M. M. Abdel-Daim. 2020. The impact of stocking density and dietary carbon sources on the growth, oxidative status and stress markers of Nile tilapia (Oreochromis niloticus) reared under biofloc conditions. Aquaculture Reports 259:100282. doi:10.1016/j.aqrep.2020.100282.
   Google Scholar