Fate of a branched nonylphenol isomer in submerged paddy soils amended with nitrate

被引:12
|
作者
Liu, Qin [1 ,2 ]
Ji, Rong [3 ]
Hommes, Gregor [2 ]
Schaeffer, Andreas [2 ]
Corvini, Philippe F. -X. [4 ]
机构
[1] Chinese Acad Sci, Inst Soil Sci, Nanjing 210008, Peoples R China
[2] Rhein Westfal TH Aachen, D-52056 Aachen, Germany
[3] Nanjing Univ, Sch Environm, State Key Lab Pollut Control & Resource Reuse, Nanjing 210093, Peoples R China
[4] Univ Appl Sci NW Switzerland FHNW, Sch Life Sci, Inst Ecopreneurship, CH-4132 Muttenz, Switzerland
基金
美国国家科学基金会;
关键词
Endocrine disrupting compounds; Nonylphenol; Submerged paddy soils; Anoxic condition; Nitrate;
D O I
10.1016/j.watres.2008.08.026
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Using a (14)C-labelled branched isomer of NP, the fate of NP was studied in two flooded typical paddy soils under anoxic conditions. Biodegradation of NP occurred under anoxic conditions and was accompanied by the production of polar metabolites and bound residues in alkaline soil extract and humin. The addition of nitrate (20 mM) increased the degradation of NP in both soils, especially in soil derived from silt loam deposit, which contained high amounts of organic matter. Less than 1% NP mineralization was detected as free CO(2) in both soils, whereas up to 30, 21, 31% of NP residues comprised at least two polar metabolites, those extractable from humic substances and from the humin fraction, respectively. The denaturing gradient gel electrophoresis (DGGE) analysis of DNA extract of the soil microorganisms hinted differences of microbial community between soils with different degradation rates of NP. The present study provides for the first time information about the fate of a branched nonylphenol isomer in submerged soils amended with nitrate. The production of high amounts of polar metabolites under anoxic conditions suggests the necessity of also considering the fate and possible effects of the degradation products of NP in anoxic environment such as in waterlogged soil. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4802 / 4808
页数:7
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