References
- Abdourahime, H., et al., 2019. Peer review of the pesticide risk assessment of the active substance thiacloprid. EFSA journal, 17, 1–45.
- Crosby, E.B., et al., 2015. Neurobehavioral impairments caused by developmental imidacloprid exposure in zebrafish. Neurotoxicology and teratology, 49, 81–90.
- Ford, K.A. and Casida, J.E., 2006. Chloropyridinyl neonicotinoid insecticides: diverse molecular substituents contribute to facile metabolism in mice. Chemical research in toxicology, 19, 9644–9951.
- Frew, J.A., et al., 2018. Toxicokinetics of the neonicotinoid insecticide imidacloprid in rainbow trout (Oncorhynchus mykiss). Comparative, environmental and evolutionary physiology. Part C: toxicology and pharmacology, 205, 34–42.
- Ge, W., et al., 2015. Oxidative stress and DNA damage induced by imidacloprid in zebrafish (Danio rerio). Journal of agricultural and food chemistry, 63, 1856–1862.
- Klein, O., 2001. Behavior of Thiacloprid in plants and animals. Pflanzenschutz-Nachrichten Bayer, 54, 209–240.
- Kolanczyk, R.C., et al., 1999. Biotransformation of 4-methoxyphenol in rainbow trout (Oncorhynchus mykiss) hepatic microsomes. Aquatic toxicology, 45, 47–61.
- Kolanczyk, R.C., et al., 2020. In vitro metabolism of imidacloprid and acetamiprid in rainbow trout and rat. Xenobiotica, 50, 805–810.
- Sanchez-Bayo, F., Goka, K., and Hayasaka, D., 2016. Contamination of the aquatic environment with neonicotinoids and its implication for ecosystems. Frontiers in environmental science, 4, 1–14.
- Schmieder, P.K., et al., 2004. Use of trout liver slices to enhance mechanistic interpretation of estrogen receptor binding for cost-effective prioritization of chemicals within large inventories. Environmental science & technology, 38, 6333–6342.
- Schymanski, E., et al., 2014. Identifying small molecules via high resolution mass spectrometry: communicating confidence. Environmental science & technology, 48, 2097–2098.
- Serrano, J., et al., 2019b. Characterization and analysis of estrogenic cyclic phenone metabolites produced in vitro by rainbow trout liver slices using GC-MS, LC-MS and LC-TOF-MS. Journal of chromatography B: analytical technologies in the biomedical and life sciences, 1126–1127, 121–127.
- Serrano, J., et al., 2019a. Metabolism of cyclic phenones in rainbow trout in vitro assays. Xenobiotica, 19, 1–17.
- Simon-Delso, N., et al., 2015. Systemic insecticides (neonicotinoids and fipronil): trends, uses, mode of action and metabolites. Environmental science and pollution research, 22, 5–34.
- Tapper, M.A., et al., 2018. Metabolism of diazinon in rainbow trout liver slices. Applied in vitro toxicology, 4, 13–23.
- Tomizawa, M., 2004. Neonicotinoids and derivatives: effects in mammalian cells and mice. Journal of pesticide science, 29, 177–183.
- Tomizawa, M. and Casida, J.E., 2003. Selective toxicity of neonicotinoids attributable to specificity of insect and mammalian nicotinic receptors. Annual review of entomology, 48, 339–364.
- Tomizawa, M. and Yamamoto, I., 1993. Structure-activity relationships of nicotinoids and imidacloprid analogs. Journal of pesticide science, 18, 91–98.
- Wood, T.J. and Goulson, D., 2017. The environmental risks of neonicotinoid pesticides: a review of the evidence post 2013. Environmental science and pollution research, 24, 17285–17325.