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可耕地土壤中氯代三嗪类除草剂及其转化产物的存在情况。

Occurrence of Chlorotriazine herbicides and their transformation products in arable soils.

作者信息

Scherr Kerstin E, Bielská Lucie, Kosubová Petra, Dinisová Petra, Hvězdová Martina, Šimek Zdeněk, Hofman Jakub

机构信息

Research Centre for Toxic Compounds in the Environment (RECETOX), Faculty of Science, Masaryk University, Kamenice 753/5, 625 00 Brno, Czechia; Institute for Environmental Biotechnology, Department for Agrobiotechnology (IFA-Tulln), University of Natural Resources and Life Sciences (BOKU), Konrad-Lorenz-Strasse 20, 3430 Tulln, Austria.

Research Centre for Toxic Compounds in the Environment (RECETOX), Faculty of Science, Masaryk University, Kamenice 753/5, 625 00 Brno, Czechia.

出版信息

Environ Pollut. 2017 Mar;222:283-293. doi: 10.1016/j.envpol.2016.12.043. Epub 2016 Dec 23.

Abstract

Chlorotriazine herbicides (CTs) are widely used pest control chemicals. In contrast to groundwater contamination, little attention has been given to the circumstances of residue formation of parent compounds and transformation products in soils. Seventy-five cultivated floodplain topsoils in the Czech Republic were sampled in early spring of 2015, corresponding to a minimum of six months (current-use terbuthylazine, TBA) and a up to a decade (banned atrazine, AT and simazine, SIM) after the last herbicide application. Soil residues of parent compounds and nine transformation products were quantified via multiple residue analysis using liquid chromatography - tandem mass spectrometry of acetonitrile partitioning extracts (QuEChERS). Using principal component analysis (PCA), their relation to soil chemistry, crops and environmental parameters was determined. Of the parent compounds, only TBA was present in more than one sample. In contrast, at least one CT transformation product, particularly hydroxylated CTs, was detected in 89% of the sites, or 54% for banned triazines. Deethylated and bi-dealkylated SIM or AT residues were not detectable. PCA suggests the formation and/or retention of CT hydroxy-metabolite residues to be related to low soil pH, and a direct relation between TBA and soil organic carbon, and between deethyl-TBA and clay or Ca contents, respectively, the latter pointing towards distinct sorption mechanisms. The low historic application of simazine contrasted by the high abundance of its residues, and the co-occurrence with AT residues suggests the post-ban application of AT and SIM banned triazines as a permitted impurity of TBA formulations as a recent, secondary source. The present data indicate that topsoils do not contain abundant extractable residues of banned parent chlorotriazines, and are thus likely not the current source for related ground- and surface water contamination. In contrast, topsoils might pose a long-term source of TBA and CT transformation products for ground and surface water contamination.

摘要

氯三嗪类除草剂(CTs)是广泛使用的害虫防治化学品。与地下水污染不同,人们很少关注母体化合物及其转化产物在土壤中残留形成的情况。2015年早春,在捷克共和国采集了75份耕种洪泛平原表层土壤样本,这些样本对应的是上次施用除草剂后至少6个月(当前使用的特丁津,TBA)至长达10年(已禁用的莠去津,AT和西玛津,SIM)的时间。通过使用乙腈分配提取物(QuEChERS)的液相色谱 - 串联质谱法进行多残留分析,对母体化合物和9种转化产物的土壤残留量进行了定量。使用主成分分析(PCA)确定了它们与土壤化学、作物和环境参数之间的关系。在母体化合物中,只有TBA在多个样本中存在。相比之下,在89%的采样点检测到至少一种CT转化产物,对于已禁用的三嗪类化合物则为54%,特别是羟基化的CTs。未检测到脱乙基和双脱烷基的SIM或AT残留。PCA表明CT羟基代谢物残留的形成和/或保留与低土壤pH值有关,TBA与土壤有机碳之间以及脱乙基TBA与粘土或钙含量之间分别存在直接关系,后者表明存在不同的吸附机制。西玛津历史施用率低,但其残留量却很高,且与AT残留共存,这表明已禁用的AT和SIM三嗪类化合物作为TBA制剂的允许杂质在禁用后仍有施用,是近期的次要来源。目前的数据表明,表层土壤中不含有大量可提取的已禁用母体氯三嗪残留,因此可能不是相关地下水和地表水污染的当前来源。相比之下,表层土壤可能是TBA和CT转化产物对地下水和地表水造成污染的长期来源。

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