首页> 外文期刊>Environmental Science & Technology >Field Validation of Anaerobic Degradation Pathways for Dichlorodiphenyltrichloroethane (DDT) and 13 Metabolites in Marine Sediment Cores from China
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Field Validation of Anaerobic Degradation Pathways for Dichlorodiphenyltrichloroethane (DDT) and 13 Metabolites in Marine Sediment Cores from China

机译:中国海洋沉积物芯中二氯二苯基三氯乙烷(DDT)和13种代谢产物的厌氧降解途径的现场验证

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摘要

Although the production and use of dichlorodiphenyltrichloroethane (DDT), a legacy component of persistent organic pollutants, have been highly restricted worldwide, the environmental fate of DDT has remained a great concern as it is not only ubiquitous and bioaccumulative but can also be degraded to a series of metabolites that may be more hazardous ecologically. The present study, taking advantage of the abundant levels of DDT and its metabolites in a subtropical coastal region of China, investigated into the degradation pathways of DDT in natural coastal sediment. Sediment profiles indicated that degradation of l,l,l-trichloro-2,2-bis-(p-chlorophenyl)ethane (p,p'-DDT) to l,l-dichloro-2,2-bis-(p-chlorophenyl)ethane (p,p'-DDD) mainly occurred in sediment of the top 20 cm layer. l,l-dichloro-2,2-bis-(p-chlorophenyl)ethylene (p,p'-DDE), aerobically transformed from p,p'-DDT prior to sedimentation, was likely to degrade to l-chloro-2,2-bis-(p-chlorophenyl)ethylene (p,p'-DDMU) which was further converted to 2,2-bis(p-chlorophe-nyl)ethylene (p,p'-DDNU). In addition, p,p'-DDNU could be transformed to 2,2-bis(p-chlorophe-nyl)ethane (p,p'-DDNS) and other high-order metabolites. On the other hand, the conversions of p, p'-DDD to/y/-DDMU and l-chloro-2,2-bis-(p-chlorophenyl)ethane (p,p'-DDMS) top,p'-DDNUwere deemed slow in anaerobic sediment. Therefore, the present study confirmed all the degradation pathways involving reductive dechlorination and p,p'-DDE being a more important precursor for p,p' -DDMU than p,p'-DDD in anaerobic sediment, as proposed previously. On the other hand, the present study suggested that p,p'-DDMU instead ofp,p' -DDMS was more likely the precursor for formation of high-order metabolites. Based on the current assessments, use of (DDD+DDE)/DDTs to indicate whether there is fresh DDT input may lead to large uncertainties if the concentrations of high-order metabolites are not negligible. Similarly, ecological risk assessment associated with DDT should be conducted with consideration of high-order DDT metabolites.
机译:尽管全世界一直严格限制持久性有机污染物的遗留成分二氯二苯基三氯乙烷(DDT)的生产和使用,但DDT的环境命运仍然令人担忧,因为它不仅无处不在且具有生物蓄积性,而且还可以降解为有机污染物。可能在生态上更具危害性的一系列代谢物。本研究利用中国亚热带沿海地区大量的DDT及其代谢产物,研究了DDT在天然沿海沉积物中的降解途径。泥沙剖面表明,l,l,1-三氯-2,2-双-(对氯苯基)乙烷(p,p'-DDT)降解为1,l-二氯-2,2-双-(p-氯苯基)乙烷(p,p'-DDD)主要发生在20 cm顶部的沉积物中。在沉淀之前由p,p'-DDT好氧转化的l,l-dichloro-2,2-双-(对氯苯基)乙烯(p,p'-DDE)可能降解为1-chloro-2 ,2-双-(对氯苯基)乙烯(p,p′-DDMU)进一步被转化为2,2-双(对氯苯甲基)乙烯(p,p′-DDNU)。此外,p,p'-DDNU可以转化为2,2-双(p-chlorophe-nyl)乙烷(p,p'-DDNS)和其他高阶代谢物。另一方面,p,p′-DDD向/ y / -DDMU和1-氯-2,2-双-(对氯苯基)乙烷(p,p′-DDMS)的转化率最高,p′- DDNU被认为是厌氧沉积物中的慢物质。因此,如先前所提出的,本研究证实了所有涉及还原脱氯的降解途径,并且p,p'-DDE是厌氧沉积物中p,p'-DDMU的重要前体,比p,p'-DDD更重要。另一方面,本研究表明,p,p'-DDMU代替p,p'-DDMS更可能是形成高阶代谢产物的前体。根据目前的评估,如果不能忽略高阶代谢物的浓度,则使用(DDD + DDE)/ DDT来指示是否有新鲜的DDT输入会导致很大的不确定性。同样,与滴滴涕有关的生态风险评估应考虑高阶滴滴涕代谢产物。

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  • 来源
    《Environmental Science & Technology》 |2011年第12期|p.5245-5252|共8页
  • 作者单位

    State Key Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences,Guangzhou 510640, China,Graduate School, Chinese Academy of Sciences, Beijing 100049, China;

    State Key Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences,Guangzhou 510640, China,Graduate School, Chinese Academy of Sciences, Beijing 100049, China;

    Department of Biology, Hong Kong Baptist University, Hong Kong SAR, China and;

    State Key Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences,Guangzhou 510640, China;

  • 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);
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  • 正文语种 eng
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  • 入库时间 2022-08-17 14:03:46

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