DEGRADATION OF TRIFLUOROACETATE IN OXIC AND ANOXIC SEDIMENTS

被引:83
作者
VISSCHER, PT
CULBERTSON, CW
OREMLAND, RS
机构
[1] US Geological Survey, Menlo Park, CA 94025
关键词
D O I
10.1038/369729a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
THE deleterious effect of chlorofluorocarbons on stratospheric ozone has led to international cooperation to end their use(1-3). The search for acceptable alternatives has focused on hydrofluorocarbons (HFCs) or hydrochlorofluorocarbons (HCFCs) which are attractive because they have relatively short atmospheric residence times(4). HFCs and HCFCs are attacked by tropospheric hydroxyl radicals, leading to the formation of trifluoroacetate (TFA)(5). Most of the atmospheric TFA is deposited at the Earth's surface(6), where it is thought to be highly resistant to bacterial attack(5). Therefore, use of HCFCs and HFCs may lead to accumulation of TFA in soils, where it could prove toxic or inhibitory to plants and soil microbial communities(5,7). Although little is known about the toxicity of TFA, monofluoroacetate, which occurs at low levels in some plants(8) and which is susceptible to slow attack by aerobic soil microbes(9), is known to be acutely toxic(10-13). Here we report that TFA can be rapidly degraded microbially under anoxic and oxic conditions. These results imply that significant microbial sinks exist in nature for the elimination of TFA from the environment. We also show that oxic degradation of TFA leads to the formation of fluoroform, a potential ozone-depleting compound with a much longer atmospheric lifetime than the parent compounds.
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页码:729 / 731
页数:3
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