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不同氧化还原条件和溶解有机物对模拟地下水中农药生物降解的影响。

Influence of different redox conditions and dissolved organic matter on pesticide biodegradation in simulated groundwater systems.

机构信息

Sub-department of Environmental Technology, Wageningen University & Research, P.O. Box 47, 6700 AA Wageningen, the Netherlands.

Laboratory of Microbiology, Wageningen University & Research, P.O. Box 47, 6700 AA Wageningen, the Netherlands.

出版信息

Sci Total Environ. 2019 Aug 10;677:692-699. doi: 10.1016/j.scitotenv.2019.04.128. Epub 2019 Apr 10.

Abstract

Insights into the influence of redox conditions, that is the availability of electron acceptors, and dissolved organic matter (DOM) on pesticide biodegradation in groundwater are key to understanding the environmental fate of pesticides in natural groundwater systems. Here, the influence of redox conditions and supplemental DOM addition on biodegradation of pesticides, 2,4-dichlorophenoxyacetic acid (2,4-D), 2,6-dichlorobenzamide (BAM), mecoprop-p (MCPP) and bentazone, was tested in microcosm and subsequent column experiments. Pesticide degradation, functional genes and changes in specific fractions and quantity of DOM were systematically quantified. In aerobic microcosm experiments, the highest 2,4-D degradation rate was obtained with the presence of more assimilable DOM. In column experiments, minimal pesticide degradation (≤33.77%) in any anaerobic redox conditions was observed in the absence of DOM. However, in the presence of DOM, 2,4-D biodegradation was considerably enhanced under nitrate-reducing conditions (from 23.5 ± 10.2% to 82.3 ± 11.6%) and in a column without external electron acceptor amendment (from -6.3 ± 12.6% to 31.1 ± 36.3%). Observed preferential depletion of the fulvic acid fraction of DOM provides indications for specific functional DOM properties. The qPCR results show an increase in microbial biomass and functional genes (tfdA) in liquid phase after DOM addition. The results of this work provide insights into the interplays among DOM, redox geochemistry, and pesticide biodegradation, and show the potential of a novel approach - DOM addition to groundwater systems - for in situ biostimulation technology to remove pesticides from groundwater systems.

摘要

了解氧化还原条件(即电子受体的可利用性)和溶解有机质(DOM)对地下水中药剂生物降解的影响,是理解天然地下水中农药环境归宿的关键。本研究中,采用微宇宙和后续柱实验,测试了氧化还原条件和补充 DOM 对 2,4-二氯苯氧乙酸(2,4-D)、2,6-二氯苯甲酰胺(BAM)、麦草畏(MCPP)和苯达松生物降解的影响。系统定量了农药降解、功能基因以及 DOM 特定分数和数量的变化。在好氧微宇宙实验中,存在更多可同化 DOM 时,2,4-D 的降解速率最高。在没有 DOM 的情况下,任何厌氧氧化还原条件下,农药的降解率均最低(≤33.77%)。然而,在有 DOM 的情况下,在硝酸盐还原条件下(从 23.5±10.2%增加到 82.3±11.6%)和在没有外部电子受体添加的柱中(从-6.3±12.6%增加到 31.1±36.3%),2,4-D 的生物降解得到了显著增强。DOM 中富里酸分数的优先耗尽为特定功能 DOM 性质提供了指示。qPCR 结果表明,DOM 加入后液相中微生物生物量和功能基因(tfdA)增加。本研究结果深入了解了 DOM、氧化还原地球化学和农药生物降解之间的相互作用,并展示了一种新方法——将 DOM 添加到地下水中——作为原位生物刺激技术从地下水中去除农药的潜力。

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