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Chiral Organochlorine Pesticide Signatures in Global Background Soils

机译:全球背景土壤中的手性有机氯农药特征

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摘要

Chiral pesticides frequently undergo enantioselective degradation in soils.Prior studies to characterize chiral signatures have focused on treated agricultural soils,rather than background (untreated) soils,and tracking signatures in the atmosphere for source apportionment purposes.In this study,we investigated the chiral signatures in 65 background soils collected from different locations across the world.The soils were taken from different ecosystems (e.g.,grasslands,forests),and the enantiomeric fractions (EFs) of chiral chlordanes,alpha-hexachlorocyclohexane (alpha-HCH),and o,p'-DDT were determined.Chlordanes in most of the soils showed the usual pattern of enantioselective degradation seen in agricultural soils,depletion of (+)-trans-chlordane (TC) and (-)-cis-chlordane (CC).However,some samples showed opposite enantiomer degradation patterns for TC,CC,and chlordane compound MC5.Correlations were tested between the deviation of EFs from racemic (DEVrac = absolute value of 0.500 - EF),the percent soil organic matter (% SOM),annual mean temperature,and the ratio of TC to the more stable compound trans-nonachlor (TN).Significant positive correlations were found between DEVrac and % SOM for TC and CC (p = 0.0022 and 0.0031),but not for the other OCPs.No significant correlations were found between DEVrac and annual mean temperature for any of the OCPs.DEVrac for TC was negatively correlated with the TC/TN ratio,but the regression was driven by two points with high ratios of TC/CC.Removing these two points resulted in a nonsignificant regression.The range of EFs for TC,CC,and alpha-HCH in soils was greater than in ambient air,providing evidence of in situ degradation after atmospheric deposition in some cases.Variable EFs in soil suggest that caution is needed when considering the enantiomer signatures in air as a marker of volatilization of weathered soil-derived organochlorines.
机译:手性农药在土壤中经常经历对映选择性降解。表征手性特征的先前研究主要集中在经过处理的农业土壤上,而不是背景(未经处理的)土壤上,并在大气中跟踪特征以进行源分配。本研究中,我们研究了手性特征在全球不同地区收集的65种背景土壤中,这些土壤分别来自不同的生态系统(例如草地,森林)以及手性氯丹,α-六氯环己烷(α-HCH)和o的对映体组分(EFs),测定了p'-DDT。大多数土壤中的氯丹显示出在农业土壤中常见的对映选择性降解模式,(+)-反式氯丹(TC)和(-)-顺式氯丹(CC)的消耗。 ,一些样品显示TC,CC和氯丹化合物MC5的对映异构体降解模式相反。测试了EF与外消旋物的偏差之间的相关性(DEVrac =绝对值0.500- EF),土壤有机质百分比(%SOM),年平均温度以及TC与更稳定的化合物反式六氯胺(TN)的比率。发现DEVrac与TC和CC的%SOM之间存在显着的正相关(p = 0.0022和0.0031),但其他OCP则不然。任何OCP的DEVrac与年平均温度之间均无显着相关.TC的DEVrac与TC / TN比呈负相关,但回归是由两个因素驱动的TC / CC比率较高的点。去除这两个点导致无显着回归。土壤中TC,CC和α-HCH的EF范围大于环境空气,提供了大气沉积后原位降解的证据土壤中的各种EFs表明,当考虑空气中的对映异构体特征作为风化的土壤衍生有机氯挥发的标志物时,需要谨慎行事。

著录项

  • 来源
    《Environmental Science & Technology》 |2005年第22期|p.8671-8677|共7页
  • 作者单位

    Environmental Science Department,Lancaster University,Lancaster,LA1 4YQ,UK,Faculty of Engineering,Department of Environmental Engineering,Akdeniz University,07200,Antalya,Turkey,and Centre for Atmospheric Research Experiments,Environment Canada,6248;

    Environmental Science Department,Lancaster University,Lancaster,LA1 4YQ,UK,Faculty of Engineering,Department of Environmental Engineering,Akdeniz University,07200,Antalya,Turkey,and Centre for Atmospheric Research Experiments,Environment Canada,6248;

    Environmental Science Department,Lancaster University,Lancaster,LA1 4YQ,UK,Faculty of Engineering,Department of Environmental Engineering,Akdeniz University,07200,Antalya,Turkey,and Centre for Atmospheric Research Experiments,Environment Canada,6248;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 环境化学;
  • 关键词

  • 入库时间 2022-08-17 14:07:57

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