Toxicity of nitrogen compounds in fish influenced by physico-chemical water parameters: a review
DOI:
https://doi.org/10.33448/rsd-v10i11.19779Keywords:
Anthropic; Nitrogen cycle; Histopathologies; Impact; Pollutants.Abstract
Nitrogen compounds (nitrite, nitrate and ammonia) are considered toxic to fish, as they can promote histological and biochemical changes, decrease the oxygen-carrying capacity in the blood and affect fitness (ie the body's fitness in terms of growth and swimming). These compounds accumulate in the aquatic environment through the excretion of aquatic organisms, decomposition of organic matter from both aquatic and adjacent terrestrial systems, and direct entry into the terrestrial system, tributaries and groundwater. The so-called global changes, such as climate and land-use changes, can enhance and intensify this entry of nitrogen compounds through human activities, such as agriculture and the release of effluents, such as domestic sewage. Fish are commonly in contact with various pollutants, and the combination of environmental factors such as temperature, pH, oxygen availability and hardness can have synergistic or antagonistic effects. However, how these environmental factors affect the toxicity of ammonia, nitrite and nitrate are not fully understood. Therefore, our objective was to review the literature to address the effects of nitrogen compounds, and how the physicochemical parameters of water affect the toxicity of these compounds.
References
Alfonso, S., Gesto, M., & Sadoul, B. (2020). Temperature increase and its effects on fish stress physiology in the context of global warming. Journal of Fish Biology, 39. https://doi.org/10.1111/jfb.14599
Côté, I. M., Darling, E. S., & Brown, C. J. (2016). Interactions among ecosystem stressors and their importance in conservation. Proceedings of the Royal Society B: Biological Sciences, 283(1824). https://doi.org/10.1098/rspb.2015.2592
Çoǧun, H. Y., & Kargin, F. (2004). Effects of pH on the mortality and accumulation of copper in tissues of Oreochromis niloticus. Chemosphere, 55(2), 277–282. https://doi.org/10.1016/j.chemosphere.2003.10.007
Dutra, F. M., Cidemar Alab, J. H., Costa Gomes, M. K., Furtado, P. S., Valenti, W. C., & Cupertino Ballester, E. L. (2019). Nitrate acute toxicity to post larvae and juveniles of Macrobrachium amazonicum (Heller, 1862). Chemosphere, 242, 125229. https://doi.org/10.1016/j.chemosphere.2019.125229
Ferrari, R. (2015). Writing narrative style literature reviews. Medical Writing, 24(4), 230–235. https://doi.org/10.1179/2047480615z.000000000329
Gao, X. Q., Fei, F., Huo, H. H., Huang, B., Meng, X. S., Zhang, T., & Liu, B. L. (2020). Impact of nitrite exposure on plasma biochemical parameters and immune-related responses in Takifugu rubripes. Aquatic Toxicology, 218, 105362. https://doi.org/10.1016/j.aquatox.2019.105362
Gao, X. Q., Fei, F., Huo, H. H., Huang, B., Meng, X. S., Zhang, T., Liu, W. Bin, & Liu, B. L. (2019). Exposure to nitrite alters thyroid hormone levels and morphology in Takifugu rubripes. Comparative Biochemistry and Physiology Part - C: Toxicology and Pharmacology, 225, 108578. https://doi.org/10.1016/j.cbpc.2019.108578
Gomez Isaza, D. F., Cramp, R. L., & Franklin, C. E. (2020). Simultaneous exposure to nitrate and low pH reduces the blood oxygen-carrying capacity and functional performance of a freshwater fish. Conservation Physiology, 8(1), 1–15. https://doi.org/10.1093/conphys/coz092
Gomez Isaza, D. F., Cramp, R. L., & Franklin, C. E. (2021). Thermal plasticity of the cardiorespiratory system provides cross-tolerance protection to fish exposed to elevated nitrate. Comparative Biochemistry and Physiology Part - C: Toxicology and Pharmacology, 240, 108920. https://doi.org/10.1016/j.cbpc.2020.108920
Grynevych, N., Sliusarenko, A., Dyman, T., Sliusarenko, S., Gutyj, B., & Kukhtyn, M. (2018). Impact of provincial water management on environment and social welfare in West of Zayanderood Basin, Iran. Ukrainian Journal of Ecology, 8(1), 41–50. https://doi.org/10.15421/2018
Ha, N. T. K., Huong, D. T. T., Phuong, N. T., Bayley, M., & Jensen, F. B. (2019). Impact and tissue metabolism of nitrite at two acclimation temperatures in striped catfish (Pangasianodon hypophthalmus). Aquatic Toxicology, 212, 154–161. https://doi.org/10.1016/j.aquatox.2019.05.008
Jimenez, J. E., & Zaniboni-Filho, E. (2013). Adaptations of the piava (Leporinus obtusidens) juvenile exposed to hypoxia. Boletim Do Instituto de Pesca, 39(4), 439–444.
Kellock, K. A., Moore, A. P., & Bringolf, R. B. (2018). Chronic nitrate exposure alters reproductive physiology in fathead minnows. Environmental Pollution, 232, 322–328. https://doi.org/10.1016/j.envpol.2017.08.004
Kim, J. H., & Kang, J. C. (2016). The immune responses in juvenile rockfish, Sebastes schlegelii for the stress by the exposure to the dietary lead (II). Environmental Toxicology and Pharmacology, 46, 211–216. https://doi.org/10.1016/j.etap.2016.07.022
Kim, J. H., Park, H. J., Hwang, I. K., Han, J. M., Kim, D. H., Oh, C. W., Lee, J. S., & Kang, J. C. (2017). Toxic effects of juvenile sablefish, Anoplopoma fimbria by ammonia exposure at different water temperature. Environmental Toxicology and Pharmacology, 54, 169–176. https://doi.org/10.1016/j.etap.2017.07.008
Kir, M., & Sunar, M. C. (2018). Acute Toxicity of Ammonia and Nitrite to Sea Bream, Sparus aurata (Linnaeus, 1758), in Relation to Salinity. Journal of the World Aquaculture Society, 49(3), 516–522. https://doi.org/10.1111/jwas.12448
Kır, M., Sunar, M. C., & Gök, M. G. (2019). Acute ammonia toxicity and the interactive effects of ammonia and salinity on the standard metabolism of European sea bass (Dicentrarchus labrax). Aquaculture, 511, 734273. https://doi.org/10.1016/j.aquaculture.2019.734273
Kubitza, F. (2019). O impacto da amônia, do nitrito e do nitrato sobre o desempenho e a saúde dos peixes e camarões. A água na aquicultura | Parte 3. 1–27.
Lefevre, S., McKenzie, D. J., & Nilsson, G. E. (2017). Models projecting the fate of fish populations under climate change need to be based on valid physiological mechanisms. Global Change Biology, 23(9), 3449–3459. https://doi.org/10.1111/gcb.13652
Li, M., Zhang, M., Qian, Y., Shi, G., & Wang, R. (2020). Ammonia toxicity in the yellow catfish (Pelteobagrus fulvidraco): The mechanistic insight from physiological detoxification to poisoning. Fish and Shellfish Immunology, 102, 195–202. https://doi.org/10.1016/j.fsi.2020.04.042
Lin, Y., Miao, L. H., Pan, W. J., Huang, X., Dengu, J. M., Zhang, W. X., Ge, X. P., Liu, B., Ren, M. C., Zhou, Q. L., Xie, J., Pan, L. kun, & Xi, B. wen. (2018). Effect of nitrite exposure on the antioxidant enzymes and glutathione system in the liver of bighead carp, Aristichthys nobilis. Fish and Shellfish Immunology, 76, 126–132. https://doi.org/10.1016/j.fsi.2018.02.015
Martinez, C. B. R., Azebedo, F., & Winkaler, E. U. (2006). Toxicidade e Efeitos da Amônia em Peixes Neotropicais. Tópicos Especiais Em Biologia Aquática e Aqüicultura, 81–95.
Mehta, K. (2017). Impact of Temperature on Contaminants Toxicity in Fish Fauna: A Review. Indian Journal of Science and Technology, 10(18), 1–6. https://doi.org/10.17485/ijst/2017/v10i18/112663
Moore, A. P., & Bringolf, R. B. (2020). Comparative Toxicity of Nitrate to Common and Imperiled Freshwater Mussel Glochidia and Larval Fishes. Archives
of Environmental Contamination and Toxicology, 78(4), 536–544. https://doi.org/10.1007/s00244-020-00708-z
Opinion, A. G. R., De Boeck, G., & Rodgers, E. M. (2020). Synergism between elevated temperature and nitrate: Impact on aerobic capacity of European grayling, Thymallus thymallus in warm, eutrophic waters. Aquatic Toxicology, 226, 105563. https://doi.org/10.1016/j.aquatox.2020.105563
Pankhurst, N. W., & Munday, P. L. (2011). Effects of climate change on fish reproduction and early life history stages. Marine and Freshwater Research, 62(9), 1015–1026. https://doi.org/10.1071/MF10269
Paul, S., Mandal, A., Bhattacharjee, P., Chakraborty, S., Paul, R., & Kumar Mukhopadhyay, B. (2019). Evaluation of water quality and toxicity after exposure of lead nitrate in fresh water fish, major source of water pollution. Egyptian Journal of Aquatic Research, 45(4), 345–351. https://doi.org/10.1016/j.ejar.2019.09.001
Randall, D. J., & Tsui, T. K. N. (2002). Ammonia toxicity in fish. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, 124, S62. https://doi.org/10.1016/s1095-6433(99)90247-7
Rodgers, E. M., Opinion, A. G. R., Gomez Isaza, D. F., Rašković, B., Poleksić, V., & De Boeck, G. (2021). Double whammy: Nitrate pollution heightens susceptibility to both hypoxia and heat in a freshwater salmonid. Science of the Total Environment, 765. https://doi.org/10.1016/j.scitotenv.2020.142777
Silva, M. J. Dos S., Costa F. B. C., Leme, F. P.; Takata, R., Costa, D. C., Matitioli, C. C., Luz, R. K., Miranda-Filho, K. C. (2017). Biological responses of Neotropical freshwater fish Lophiosilurus alexandri exposed to ammonia and nitrite. Science of the Total Environment, 616–617, 1566–1575.
Vitousek, P. M., Mooney, H. A., Lubchenco, J., Melillo, J. M. (1997). Human Domination of Earth Ecosystems. Science, 278(5335), 494–499.
Wang, J., Tang, H., Zhang, X., Xue, X., Zhu, X., Chen, Y., & Yang, Z. (2017). Mitigation of nitrite toxicity by increased salinity is associated with multiple physiological responses: A case study using an economically important model species, the juvenile obscure puffer (Takifugu obscurus). Environmental Pollution, 232, 137–145. https://doi.org/10.1016/j.envpol.2017.09.026
Wang, Y., Kong, X., Peng, Z., Zhang, H., Hu, W., & Zhou, X. (2020) Retenção de nitrogênio e fósforo no Lago Chaohu, China: implicações para o manejo da eutrofização. Environmental Science and Pollution Research. 27, 41488–41502. https://doi.org/10.1007/s11356-020-10024-7
Yang, Z., & Chen, Y. (2006). Salinity tolerance of embryos of obscure puffer Takifugu obscurus. Aquaculture, 253(1–4), 393–397. https://doi.org/10.1016/j.aquaculture.2005.08.014
Zhang, W., Xia, S., Zhu, J., Miao, L., Ren, M., Lin, Y., Ge, X., & Sun, S. (2019). Growth performance, physiological response and histology changes of juvenile blunt snout bream, Megalobrama amblycephala exposed to chronic ammonia. Aquaculture, 506, 424–436. https://doi.org/10.1016/j.aquaculture.2019.03.072
Zhao, L., Cui, C., Liu, Q., Sun, J., He, K., Adam, A. A., Luo, J., Li, Z., Wang, Y., & Yang, S. (2020). Combined exposure to hypoxia and ammonia aggravated biological effects on glucose metabolism, oxidative stress, inflammation and apoptosis in largemouth bass (Micropterus salmoides). Aquatic Toxicology, 224, 105514. https://doi.org/10.1016/j.aquatox.2020.105514
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Copyright (c) 2021 Thaís Paula de Araújo; Ludmila Silva Brighenti; Hélio Batista dos Santos; Ana Hortência Fonseca Castro; Ralph Gruppi Thomé
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