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土壤中低浓度有机化合物的矿化动力学

Kinetics of mineralization of organic compounds at low concentrations in soil.

作者信息

Scow K M, Simkins S, Alexander M

出版信息

Appl Environ Microbiol. 1986 May;51(5):1028-35. doi: 10.1128/aem.51.5.1028-1035.1986.

Abstract

The kinetics of mineralization of 14C-labeled phenol and aniline were measured at initial concentrations ranging from 0.32 to 5,000 ng and 0.30 ng to 500 micrograms/g of soil, respectively. Mineralization of phenol at concentrations less than or equal to 32 ng/g of soil and of aniline at all concentrations began immediately, and the curves for the evolution of labeled CO2 were biphasic. The patterns of mineralization of 4.0 ng of 2,4-dichlorophenol per g of soil and 20 ng of nitrilotriacetic acid per g of soil were similar to the patterns for phenol and aniline. The patterns of mineralization of 1.0 to 100 ng of p-nitrophenol and 6.0 ng of benzylamine per g of soil were also biphasic but after a short apparent lag period. The curves of CO2 evolution from higher concentrations of phenol and p-nitrophenol had increasing apparent lag phases and were S-shaped or linear. Cumulative plots of the percentage of substrate converted to CO2 were fit by nonlinear regression to first-order, integrated Monod, logistic, logarithmic, zero-order, three-half-order, and two-compartment models. None of the models of the Monod family provided the curve of best fit to any of the patterns of mineralization. The linear growth form of the three-half-order model provided the best fit for the mineralization of p-nitrophenol, with the exception of the lowest concentrations, and of benzylamine. The two-compartment model provided the best fit for the mineralization of concentrations of phenol below 100 ng/g, of several concentrations of aniline, and of nitrilotriacetic acid. It is concluded that models derived from the Monod equation, including the first-order model, do not adequately describe the kinetics of mineralization of low concentrations of chemicals added to soil.

摘要

分别在初始浓度范围为0.32至5000纳克/克土壤以及0.30纳克至500微克/克土壤的条件下,测定了14C标记的苯酚和苯胺的矿化动力学。土壤中浓度小于或等于32纳克/克的苯酚以及所有浓度的苯胺的矿化立即开始,标记二氧化碳释放曲线呈双相。每克土壤中4.0纳克2,4 - 二氯苯酚和20纳克次氮基三乙酸的矿化模式与苯酚和苯胺的模式相似。每克土壤中1.0至100纳克对硝基苯酚和6.0纳克苄胺的矿化模式也是双相的,但经过短暂的明显延迟期。较高浓度苯酚和对硝基苯酚的二氧化碳释放曲线具有逐渐增加的明显延迟期,呈S形或线性。将底物转化为二氧化碳的百分比的累积图通过非线性回归拟合到一级、积分莫诺德、逻辑斯蒂、对数、零级、三分之二级和双室模型。莫诺德家族的任何模型都没有为任何矿化模式提供最佳拟合曲线。三分之二级模型的线性增长形式为对硝基苯酚(除最低浓度外)和苄胺的矿化提供了最佳拟合。双室模型为浓度低于100纳克/克的苯酚、几种浓度的苯胺以及次氮基三乙酸的矿化提供了最佳拟合。得出的结论是,源自莫诺德方程的模型,包括一级模型,不能充分描述添加到土壤中的低浓度化学物质的矿化动力学。

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