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Evidence of biodegradation of atmospheric carbon tetrachloride in soils: Field and microcosm studies.

机译:大气中四氯化碳在土壤中的生物降解证据:田间研究和微观研究。

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摘要

Soils are thought to be sinks for atmospheric CCl4. To provide evidence of CCl4 degradation by soils, a two-year soil air samples monitoring program was initiated in New York and New Jersey. Greenhouse gases were also monitored along with CCl4, i.e. CFC-11, CFC-12, CFC-113, and CHCl3.; Soil air depth profiles showed that degradation of atmospheric CCl 4 occurred in all tested soils, and was affected by soil properties such as TOM and pH. Degradation rate constants at Sparkill, NY, were estimated as 0.6 d-1, 0.2 d-1, and 0.05 d-1 for soil depth segments of 0-1 m, 1-2m, and 2-3m, respectively. A time series of CCl4 concentrations at Sparkill, NY, showed a seasonal cycle with enhanced degradation in spring.; Microcosm studies were performed with unsaturated soil samples from Sparkill, NY, under controlled aerobic and anaerobic environments with methanol as the primary substrate, to determine whether atmospheric CCl4 degradation is biological in nature. Results suggested that indigenous soil microorganisms were responsible for the degradation. The pseudo-first order CCl4 degradation rate constants ranged from 0.04 +/- 0.01 d-1 to 0.56 +/- 0.02 d-1 at 20 °C in the aerobic microcosms, and were about 0.14 +/- 0.02 d-1 in the anaerobic microcosms at 20 °C. This is the first time that such rate constants have been reported for ppt levels of background atmospheric CCl4 in soils.; Field soil air profiles of CHCl3 indicated that it was formed rather than degraded in soils. It is speculated that abiotic mechanisms contributed to the formation of CHCl3 along with biotic processes.; Field soil air profiles of CFCs indicated that CFCs could be considered stable enough with soil depth. In contrast, the microcosm study showed that when native microorganisms were stimulated with appropriate substrates they could transform CFC-11 by both aerobic and anaerobic attack, and CFC-12 under anaerobic conditions.; To conclude, a number of processes investigated in this study contribute to the transformation of compounds of CCl4, CHCl3, CFC-11 and CFC-12 in soils.
机译:人们认为土壤是大气中CCl4的汇。为了提供土壤降解CCl4的证据,纽约和新泽西州启动了一项为期两年的土壤空气样品监测计划。还监测了温室气体以及CCl4,即CFC-11,CFC-12,CFC-113和CHCl3。土壤空气深度剖面显示,大气中的CCl 4降解在所有测试土壤中均发生,并且受土壤性质(如TOM和pH)影响。对于土壤深度为0-1 m,1-2m和2-3m的土壤段,纽约州Sparkill的降解速率常数估计分别为0.6 d-1、0.2 d-1和0.05 d-1。纽约州Sparkill的CCl4浓度的时间序列显示出春季周期增加,春季降解加剧。在控制的需氧和厌氧环境下,以甲醇为主要基质,对纽约州Sparkill的不饱和土壤样品进行了微观研究,以确定大气中CCl4的降解是否具有生物学性质。结果表明,本地土壤微生物是造成降解的原因。拟一阶CCl4降解速率常数在好氧微观世界中在20°C时的范围从0.04 +/- 0.01 d-1到0.56 +/- 0.02 d-1,在有氧微观世界中约为0.14 +/- 0.02 d-1。 20°C下的厌氧微观世界。这是首次针对土壤中背景大气CCl4的ppt水平报告这种速率常数。 CHCl3的田间土壤空气剖面表明,它是在土壤中形成而不是降解。据推测,非生物机制与生物过程一起促进了CHCl3的形成。氟氯化碳的田间土壤空气剖面表明,氟氯化碳被认为在土壤深度下足够稳定。相反,微观研究表明,当用适当的底物刺激天然微生物时,它们可以通过有氧和厌氧攻击转化为CFC-11,而在厌氧条件下转化为CFC-12。总而言之,这项研究中研究的许多过程都有助于土壤中CCl4,CHCl3,CFC-11和CFC-12化合物的转化。

著录项

  • 作者

    Liu, Xue-Feng.;

  • 作者单位

    Columbia University.;

  • 授予单位 Columbia University.;
  • 学科 Biology Microbiology.; Engineering Environmental.
  • 学位 D.E.S.
  • 年度 2006
  • 页码 139 p.
  • 总页数 139
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 微生物学;环境污染及其防治;
  • 关键词

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