Effect of size-fractionation dissolved organic matter on the mobility of prometryne in soil

被引:65
作者
Chen, Guang [1 ,2 ]
Lin, Chao [1 ]
Chen, Liang [1 ]
Yang, Hong [1 ,2 ]
机构
[1] Nanjing Agr Univ, Coll Sci, Dept Appl Chem, Nanjing 210095, Peoples R China
[2] Nanjing Agr Univ, Minist Agr, Key Lab Monitoring & Management Crop Dis & Pest I, Nanjing 210095, Peoples R China
基金
中国国家自然科学基金;
关键词
DOM; Molecular weight; Prometryne; Mobility; Structure; SORPTION-DESORPTION; PESTICIDE MOBILITY; HUMIC SUBSTANCES; FIELD; CHROMATOGRAPHY; CHLOROTOLURON; CONSTITUENTS; DEGRADATION; RESIDUES; MARINE;
D O I
10.1016/j.chemosphere.2010.03.038
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Import of organic materials in the form of compost, sludge or plant residues introduces large amounts of dissolved organic matter (DOM) into soils. DOM as a dynamic soil component affects the behaviors of organic pollutants. Different DOM constituents may affect herbicide action in a different way. However, the process of interaction between the distinct DOM-fractions and herbicides is largely unknown. In this study, DOM was separated by size-fractionation into three molecular size groups: MW < 3500 Da, 3500 Da < MW < 14 000 Da, and MW > 14 000 Da. Effects of DOM-fractions on prometryne sorption/desorption and mobility were analyzed using approaches of batch experiments, soil column and soil thin-layer chromatography. Application of varied DOM-fractions at 50 mg DOC L-1 to the soil reduced the sorption and increased desorption of prometryne. DOM-fraction with MW > 14 000 Da appeared most effective in prometryne mobilization in the soil than any other fractions. Finally, DOM-fractions were characterized by chemical analyses, fourier transformed infrared spectroscopy (FT-IR) and excitation-emission matrices (EEMs) fluorescence spectroscopy. Our studies revealed that the high-molecular weight fraction contained more aromatic framework and unsaturated structure that was most likely the dominant factor modulating the behavior of prometryne in soils. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1046 / 1055
页数:10
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