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Analysis of glyphosate degradation in a soil microcosm

机译:草甘膦在土壤微观世界中的降解分析

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摘要

AbstractGlyphosate (GLP) herbicide leaching into soil can undergo abiotic degradation and two enzymatic oxidative or hydrolytic reactions in both aerobic and anaerobic conditions; biotic oxidation produces aminomethylphosphonic acid (AMPA). Both GLP and AMPA are phytotoxic. A comprehensive GLP degradation reaction network was developed from the literature to account for the above pathways, and fifteen experimental data sets were used to determine the corresponding Michaelis-Menten-Monod (MMM) kinetic parameters. Various sensitivity analyses were designed to assess GLP and AMPA degradation potential againstO2(aq) and carbon (C) availability, pH, and birnessite mineral content, and showed that bacteria oxidized or hydrolyzed up to 98% of GLP and only 9% of AMPA. Lack of a C source limited the GLP cometabolic hydrolytic pathways, which produces non-toxic byproducts and promotes AMPA biodegradation. Low bacterial activity inO2(aq)-limited conditions or non-neutral pH resulted in GLP accumulation. Birnessite mineral catalyzed fast GLP and AMPA chemodegradation reaching alone efficiencies of 79% and 88%, respectively, regardless of the other variables and produced non-toxic byproducts. Overall,O2(aq) and birnessite availability played the major roles in determining the partitioning of GLP and its byproducts mass fluxes across the reaction network, while birnessite, C availability, and pH affected GLP and AMPA biodegradation effectiveness.Graphical abstractDisplay OmittedHighlightsA comprehensive glyphosate biochemical reaction network was developed.One functional group biodegraded up to 100% of injected glyphosate.Various environmental conditions substantially decreased glyphosate biodegradation.Glyphosate chemical degradation can overcome limited bacterial activity.GLP and AMPA persisted in anoxic or extreme acidic and basic environments posing a risk of environmental pollution. The risk was negligible as birnessite mineral chemically degraded GLP to sarcosine.
机译: 摘要 草甘膦(GLP)除草剂浸入土壤可能会在有氧和厌氧条件下发生非生物降解和两种酶促氧化或水解反应;生物氧化产生氨基甲基膦酸(AMPA)。 GLP和AMPA均具有植物毒性。从文献中开发了一个综合的GLP降解反应网络来解释上述途径,并使用15个实验数据集确定相应的Michaelis-Menten-Monod(MMM)动力学参数。设计了各种敏感性分析,以针对 O 2 (aq)和碳(C)的可用性,pH值和水钠锰矿矿物质含量,表明细菌氧化或水解的GLP高达98%,AMPA仅为9%。缺乏碳源限制了GLP的新陈代谢水解途径,该途径可产生无毒副产物并促进AMPA生物降解。 O 2 ( aq)限制条件或非中性pH导致GLP积累。不论其他变量如何,水钠锰矿矿物催化的GLP和AMPA快速化学降解分别达到79%和88%的效率,并产生无毒的副产物。总体而言, O 2 (aq)碳酸钙和水钠锰矿的可用性在决定GLP及其副产物在整个反应网络中的通量的分配中起着主要作用,而碳酸氢钠水钠,C的有效性和pH值会影响GLP和AMPA的生物降解效果。 图形摘要 省略显示 突出显示 < ce:simple-para id =“ abspara0020” view =“ all”> 开发了一个全面的草甘膦生化反应网络。 一个官能团可生物降解多达100%的草甘膦。 各种环境条件均大大降低了草甘膦的生物降解能力。 草甘膦的化学降解可以克服有限的细菌活性。 GLP和AMPA持续在缺氧或极端酸性和碱性环境中构成环境污染的风险。由于水钠锰矿矿物化学降解GLP成为肌氨酸的风险可以忽略不计。

著录项

  • 来源
    《Environmental pollution》 |2018年第2期|201-207|共7页
  • 作者单位

    Laboratory for Environmental Engineering, School of Civil Engineering, The University of Sydney;

    Laboratory for Environmental Engineering, School of Civil Engineering, The University of Sydney;

  • 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

    Glyphosate; AminoMethylPhosphonic acid; Herbicide; Biodegradation; Birnessite;

    机译:草甘膦;氨基甲基膦酸;除草剂;生物降解;水钠锰矿;
  • 入库时间 2022-08-17 13:25:45

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