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在土壤和水沉积物中,丙硫菌唑及其代谢物的吸附和降解,及其对瓦氏雅罗鱼的联合毒性。

Sorption and degradation of prothioconazole and its metabolites in soils and water sediments, and its combinative toxicity to Gobiocypris rarus.

机构信息

State Key Laboratory for Biology of Plant Disease and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, 100193, China.

State Key Laboratory for Biology of Plant Disease and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, 100193, China.

出版信息

Chemosphere. 2022 Sep;303(Pt 3):135282. doi: 10.1016/j.chemosphere.2022.135282. Epub 2022 Jun 9.

Abstract

To reduce detrimental effects to the environment, the application of prothioconazole and its metabolites requires comprehensive evaluation, which has been dine for the first time in this study. The behavior of prothioconazole, including degradation and sorption under aerobic and anaerobic conditions, was evaluated in three common soil types and two types of water-sediment systems under different environmental conditions. Individual and joint toxicities of prothioconazole and its metabolites, M01 and M04, on aquatic organisms, including the Gobiocypris rarus, are also investigated in the present study. Under aerobic and anaerobic conditions, the half-life of prothioconazole in the three types of soils ranged from 0.0565 to 2.27 days and 0.138-1.73 days, respectively. Under aerobic conditions, the half-life of prothioconazole in the Hunan paddy area and Beijing Qidu reservoir water-sediment samples were 2.18 and 1.58 days, respectively. In soil and water-sediment samples, prothioconazole degraded to M01 and M04, and the formation rate of M04 was higher than M01 under aerobic condition. M04 and M01 gradually increased to a peak value in soil and water-sediment systems, then decreased over time, while prothioconazole gradually decreased. The half-life of prothioconazole in soils was lower than its metabolites, with the DT of metabolites ranging from 16.6 to 99.6 days, 15.8 and 50.7 days for M01 and M04 under aerobic condition, respectively. While the adsorption capacities (K values) of M04 and M01 ranged from 2.09 to 88.92 and 8.98 to 243.30 (μg/g)/(mg/L), respectively, in the three soils. Regarding toxicity to aquatic organisms, the metabolites did not show higher toxicity than prothioconazole, except M01 on Gobiocypris rarus. Joint toxicity assays showed that mixtures of prothioconazole with its metabolites exhibited higher toxicity than any compound individually and indicated synergistic interactions could occur at equitoxic ratios and equivalent concentrations. This study provides a comprehensive investigation on the fate and environmental risk posed by prothioconazole.

摘要

为了减少对环境的有害影响,需要对丙硫菌唑及其代谢物的应用进行全面评估,本研究首次对此进行了评估。在三种常见土壤类型和两种水-沉积物系统中,评估了丙硫菌唑在有氧和无氧条件下的降解和吸附行为,以及在不同环境条件下的行为。本研究还调查了丙硫菌唑及其代谢物 M01 和 M04 对水生生物(包括泥鳅)的单一和联合毒性。在有氧和无氧条件下,丙硫菌唑在三种土壤中的半衰期分别为 0.0565 至 2.27 天和 0.138 至 1.73 天。在有氧条件下,丙硫菌唑在湖南稻田和北京七里渡水库水-沉积物样品中的半衰期分别为 2.18 和 1.58 天。在土壤和水-沉积物样品中,丙硫菌唑降解为 M01 和 M04,有氧条件下 M04 的生成率高于 M01。M04 和 M01 在土壤和水-沉积物系统中逐渐增加到峰值,然后随时间下降,而丙硫菌唑逐渐下降。丙硫菌唑在土壤中的半衰期低于其代谢物,代谢物的 DT 分别为 16.6 至 99.6 天,M01 和 M04 分别为 15.8 和 50.7 天,在有氧条件下。而 M04 和 M01 的吸附容量(K 值)分别为 2.09 至 88.92 和 8.98 至 243.30(μg/g)/(mg/L),在三种土壤中。关于对水生生物的毒性,除了 M01 对泥鳅外,代谢物没有表现出比丙硫菌唑更高的毒性。联合毒性试验表明,丙硫菌唑与其代谢物的混合物表现出比任何单一化合物更高的毒性,表明在等毒性比和等浓度下可能发生协同作用。本研究对丙硫菌唑的归趋和环境风险进行了全面调查。

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