References
- Abdel-Hameid NAH. A protective effect of calcium carbonate against arsenic toxicity of the Nile catfish, Clarias gariepinus. Turk J Fish Aquat Sci. 2009;9:2.
- Alwan SF, Hadi AA, Shokr AE. Alterations in hematological parameters of fresh water fish, Tilapia zillii, exposed to aluminum. Journal of Science and its Applications. 2009;3:12-9.
- Bagnyukova TV, Lushchak OV, Storey KB, Lushchak VI. Oxidative stress and antioxidant defense responses by goldfish tissues to acute change of temperature from 3 to 23 C. J Therm Biol. 2007;32:227-34. https://doi.org/10.1016/j.jtherbio.2007.01.004
- Bears H, Richards JG, Schulte PM. Arsenic exposure alters hepatic arsenic species composition and stress-mediated gene expression in the common killifish (Fundulus heteroclitus). Aquat Toxicol. 2006;77:257-66. https://doi.org/10.1016/j.aquatox.2005.12.008
- Besson M, Vandeputte M, Van Arendonk JAM, Aubin J, De Boer IJM, Quillet E, Komen H. Influence of water temperature on the economic value of growth rate in fish farming: the case of sea bass (Dicentrarchus labrax) cage farming in the Mediterranean. Aquaculture. 2016;462:47-55. https://doi.org/10.1016/j.aquaculture.2016.04.030
- Beyers DW, Rice JA, Clements WH, Henry CJ. Estimating physiological cost of chemical exposure: integrating energetics and stress to quantify toxic effects in fish. Can J Fish Aquat Sci. 1999;56:814-22. https://doi.org/10.1139/f99-006
- Byun SG, Nam MM, Lee BI, Lee JH, Kim YC. Manual of starry flounder culture. National Institute of Fisheries Science, vol. 2009; 2009. p. 1-131.
- Canivet V, Chambon P, Gibert J. Toxicity and bioaccumulation of arsenic and chromium in epigean and hypogean freshwater macroinvertebrates. Arch Environ Contam Toxicol. 2001;40:345-54. https://doi.org/10.1007/s002440010182
- Canli M, Atli G. The relationships between heavy metal (Cd, Cr, Cu, Fe, Pb, Zn) levels and the size of six Mediterranean fish species. Environ Pollut. 2003;121:129-36. https://doi.org/10.1016/S0269-7491(02)00194-X
- Carvalho CS, Fernandes MN. Effect of temperature on copper toxicity and hematological responses in the neotropical fish Prochilodus scrofa at low and high pH. Aquaculture. 2006;251:109-17. https://doi.org/10.1016/j.aquaculture.2005.05.018
- Chang YJ, Hur JW, Lim HK, Lee JK. Stress in olive flounder (Paralichthys olivaceus) and fat cod (Hexagrammos otakii) by the sudden drop and rise of water temperature. Korean J Fish Aquat Sci. 2001;34:91-7.
- Cockell KA, Hilton JW, Bettger WJ. Chronic toxicity of dietary disodium arsenate heptahydrate to juvenile rainbow trout (Oncorhynchus mykiss). Arch Environ Contam Toxicol. 1991;21:518-27. https://doi.org/10.1007/BF01183873
- Datta S, Ghosh D, Saha DR, Bhattacharaya S, Mazumder S. Chronic exposure to low concentration of arsenic is immunotoxic to fish: role of head kidney macrophages as biomarkers of arsenic toxicity to Clarias batrachus. Aquat Toxicol. 2009;92:86-94. https://doi.org/10.1016/j.aquatox.2009.01.002
- Farkas A, Salanki J, Specziar A. Relation between growth and the heavy metal concentration in organs of bream Abramis brama L. populating Lake Balaton. Arch Environ Contam Toxicol. 2002;43:236-43. https://doi.org/10.1007/s00244-002-1123-5
- Farombi EO, Adelowo OA, Ajimoko YR. Biomarkers of oxidative stress and heavy metal levels as indicators of environmental pollution in African cat fish (Clarias gariepinus) from Nigeria Ogun River. Int J Environ Res Public Health. 2007;4:158-65. https://doi.org/10.3390/ijerph2007040011
- Ferrario D, Croera C, Brustio R, Collotta A, Bowe G, Vahter M, Gribaldo L. Toxicity of inorganic arsenic and its metabolites on haematopoietic progenitors "in vitro": comparison between species and sexes. Toxicology. 2008;249:102-8. https://doi.org/10.1016/j.tox.2008.04.008
- Handeland SO, Imsland AK, Stefansson SO. The effect of temperature and fish size on growth, feed intake, food conversion efficiency and stomach evacuation rate of Atlantic salmon post-smolts. Aquaculture. 2008;283:36-42. https://doi.org/10.1016/j.aquaculture.2008.06.042
- Harris RC, Bodaly RD. Temperature, growth and dietary effects on fish mercury dynamics in two Ontario lakes. Biogeochemistry. 1998;40:175-87. https://doi.org/10.1023/A:1005986505407
- Hayat S, Javed M, Razzaq S. Growth performance of metal stressed major carps viz. Catla catla, Labeo rohita and Cirrhina mrigala reared under semi-intensive culture system. Pak Vet J. 2007;27:8.
- Hussain SM, Javed M, Asghar S, Hussain M, Abdullah S, Raza SA, Javid A. Studies on growth performance of metals mixture stressed Cirrhina mrigala in earthen ponds. Pak J Agri Sci. 2010;47:263-70.
- Kavitha C, Malarvizhi A, Kumaran SS, Ramesh M. Toxicological effects of arsenate exposure on hematological, biochemical and liver transaminases activity in an Indian major carp, Catla catla. Food Chem Toxicol. 2010;48:2848-54. https://doi.org/10.1016/j.fct.2010.07.017
- Lavanya S, Ramesh M, Kavitha C, Malarvizhi A. Hematological, biochemical and ionoregulatory responses of Indian major carp Catla catla during chronic sublethal exposure to inorganic arsenic. Chemosphere. 2011;82:977-85. https://doi.org/10.1016/j.chemosphere.2010.10.071
- Lushchak VI, Bagnyukova TV. Temperature increase results in oxidative stress in goldfish tissues. 2. Antioxidant and associated enzymes. Comp Biochem Physiol, Part C: Toxicol Pharmacol. 2006;143:36-41. https://doi.org/10.1016/j.cbpc.2005.11.018
- Haematological studies of freshwater catfish Mystus Vittatus exposed to sodium arsenate. Int. journal of pure and applied Zoology. 2013;1:4.
- Min E, Jeong JW, Kang JC. Thermal effects on antioxidant enzymes response in Tilapia, Oreochromis niloticus exposed arsenic. J Fish pathol. 2014;27:115-25. https://doi.org/10.7847/jfp.2014.27.2.115
- Ogata T, Ishimaru T, Kodama M. (1987). Effect of water temperature and light intensity on growth rate and toxicity change in Protogonyaulax tamarensis. Mar Biol. 1987;95:217-20. https://doi.org/10.1007/BF00409008
- Pedlar RM, Ptashynski MD, Evans R, Klaverkamp JF. Toxicological effects of dietary arsenic exposure in lake whitefish (Coregonus clupeaformis). Aquat Toxicol. 2002;57:167-89. https://doi.org/10.1016/S0166-445X(01)00198-9
- Pratap HB, Fu H, Lock RAC, Bonga SW. Effect of waterborne and dietary cadmium on plasma ions of the teleost Oreochromis mossambicus in relation to water calcium levels. Arch Environ Contam Toxicol. 1989;18:568-75. https://doi.org/10.1007/BF01055024
- Ribeiro CO, Vollaire Y, Sanchez-Chardi A, Roche HELENE. Bioaccumulation and the effects of organochlorine pesticides, PAH and heavy metals in the eel (Anguilla anguilla) at the Camargue Nature Reserve, France. Aquat Toxicol. 2005;74:53-69. https://doi.org/10.1016/j.aquatox.2005.04.008
- Roy S, Bhattacharya S. Arsenic-induced histopathology and synthesis of stress proteins in liver and kidney of Channa punctatus. Ecotoxicol Environ Saf. 2006;65:218-29. https://doi.org/10.1016/j.ecoenv.2005.07.005
- Schlenk D, Wolford L, Chelius M, Steevens J, Chan KM. Effect of arsenite, arsenate, and the herbicide monosodium methyl arsonate (MSMA) on hepatic metallothionein expression and lipid peroxidation in channel catfish. Comp Biochem Physiol, Part C: Pharmacol, Toxicol Endocrinol. 1997;118:177-83. https://doi.org/10.1016/S0742-8413(97)00083-2
- Singh AK, Banerjee TK. Toxic effects of sodium arsenate (Na2HAsO4x7H2O) on the skin epidermis of air-breathing catfish Clarias batrachus (L.). Vet Arh. 2008;78:73-88.
- Woodward DF, Brumbaugh WG, Delonay AJ, Little EE, Smith CE. Effects on rainbow trout fry of a metals-contaminated diet of benthic invertebrates from the Clark Fork River, Montana. Trans Am Fish Soc. 1994;123:51-62. https://doi.org/10.1577/1548-8659(1994)123<0051:EORTFO>2.3.CO;2
Cited by
- Experimental Approaches for Characterizing the Endocrine-Disrupting Effects of Environmental Chemicals in Fish vol.11, 2019, https://doi.org/10.3389/fendo.2020.619361
- Sublethal Effects of Arsenic on Oxygen Consumption, Hematological and Gill Histopathological Indices in Chanos chanos vol.18, pp.24, 2021, https://doi.org/10.3390/ijerph182412967
- Aspalathus Linearis extract ameliorate Haematological disorder, Dyslipidaemia and Tissue toxicity associated with Arsenic exposure in Rats vol.2, pp.1, 2019, https://doi.org/10.1016/j.phyplu.2021.100171