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Assessment of hexachlorcyclohexane biodegradation in contaminated soil by compound-specific stable isotope analysis

机译:复合特异性稳定同位素分析评估含六氯环己烷生物降解的污染土壤

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摘要

Compound-specific isotope analysis (CSIA) was firstly applied to explore the biodegradation of hexachlorcyclohexane (HCH) isomers in contaminated soil. Concentrations and compound-specific carbon isotope ratio profiles of HCH in different specific ex-situ pilot-scale contaminated soil mesocosms were determined. The addition of nutrients and Sphingobium spp. significantly enhanced the degradation of HCH in contaminated soils within 90 days. Isomer specific biodegradation of HCHs was observed with alpha- and gamma-HCH being more degradable than beta and delta-HCH. Stable carbon isotope fractionation of HCH was observed and the delta C-13 values shifted from -28.8 +/- 0.3 parts per thousand to -24.8 +/- 0.7 parts per thousand upon 87.3% removal, -27.9 +/- 0.2 parts per thousand to -25.9 +/- 0.5 parts per thousand upon 72.8% removal, -29.4 +/- 0.3 parts per thousand to -19.9 +/- 0.6 parts per thousand upon 95.8% removal, and -27.8 +/- 0.5 parts per thousand to 23.6 +/- 0.7 parts per thousand after 96.9% removal for alpha, beta, gamma, and delta-HCH, respectively. Furthermore, the enrichment factor epsilon for alpha, beta, gamma, and delta-HCH biodegradation in soil was obtained for the first time as -2.0 parts per thousand, -1.5 parts per thousand, -3.2 parts per thousand, and -1.4 parts per thousand, which could play a critical role in assessing in situ biodegradation of HCH isomers in field site soil. Results from ex-situ pilot-scale experiments clearly demonstrated that CSIA could be a promising tool to qualitatively and quantitatively evaluate in situ biodegradation of HCH in contaminated field site. (C) 2019 Elsevier Ltd. All rights reserved.
机译:首先应用复合特异性同位素分析(CSIA)以探讨含有污染土壤中六氯环己烷(HCH)异构体的生物降解。确定浓度和特异性碳同位素比例的HCH在不同特异的前原位试验型污染土壤中核科姆斯。添加营养素和鞘盆SPP。在90天内显着提高了污染土壤中的汞的降解。使用α-和γ-HCH观察到HCH的特异性生物降解比β和δ-HCH更可降解。观察HCH的稳定碳同位素分馏,ΔC-13值从-28.8 +/- 0.3左右移位至-24.8 + 0.7份每千份87.3%,-27.9 +/- 0.2零件达到-25.9 +/- 0.5份,每千份72.8%左右,-29.4 +/- 0.3份每千份至-19.9 +/- 0.6零件均为95.8%,达到-27.8 +/- 0.5零件分别在96.9%以α,β,γ和δ-hch分别达到96.9%后的每千份。此外,将α,β,γ和Delta-HCH生物降解的富集因子ε在土壤中的第一次获得-2.0份每千份,-1.5份每千份,-3.2份/份每千份,-1.4份一千,这可能在评估现场土壤中的原位生物降解方面发挥关键作用。出于原位试验规模实验的结果清楚地表明,CSIA可能是有希望的工具,以定性和定量评估污染场地中的HCH的原位生物降解。 (c)2019 Elsevier Ltd.保留所有权利。

著录项

  • 来源
    《Environmental pollution》 |2019年第1期|113008.1-113008.8|共8页
  • 作者单位

    Shenzhen Univ Shenzhen Key Lab Environm Chem & Ecol Remediat Coll Chem & Environm Engn Shenzhen 518060 Peoples R China;

    South Cent Univ Nationalities Coll Resources & Environm Sci Wuhan 430079 Hubei Peoples R China;

    UFZ Helmholtz Ctr Environm Res Dept Isotope Biogeochem Permoserstr 15 D-04318 Leipzig Germany;

    Shenzhen Univ Shenzhen Key Lab Environm Chem & Ecol Remediat Coll Chem & Environm Engn Shenzhen 518060 Peoples R 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);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Carbon isotope fractionation; Persistent organic pollutants (POPs); Bioremediation of contaminated soil; Biodegradation; Biostimulation;

    机译:碳同位素分馏;持久性有机污染物(POPs);污染土壤生物修复;生物降解;生物刺激;

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