Locke Martin A, Zablotowicz Robert M, Steinriede R Wade, Kingery William L
Water Quality & Ecology Research Unit, Agricultural Research Service, U.S. Department of Agriculture, Oxford, MS 38655, USA.
J Agric Food Chem. 2007 Feb 7;55(3):844-51. doi: 10.1021/jf062070g.
Soil sorption and dissipation of fluometuron (FLM) and three metabolites, desmethyl fluometuron (DMF), trifluoromethyl phenyl urea (TFMPU), and trifluoromethyl aniline (TFMA), were assessed in conservation tillage soils. In study I, surface Dundee silt loam soils from no-tillage (NT) and reduced-tillage (RT) areas were treated with 14C ring-labeled FLM or TFMA or unlabeled DMF, incubated for 34-42 days, extracted, and analyzed. Mineralization and volatilization of 14C-labeled FLM or TFMA were monitored. In study II, batch sorption assays (solute concentrations 2-50 micromol L-1; 2:1 solution:soil; 18 h) were conducted using various soils from reduced- (RT) and conventional-tillage (CT) areas to determine the relative affinity of FLM and metabolites for soils with differing characteristics. Mineralization of FLM (3%, day 42) or TFMA (4%, day 34) and FLM volatilization (approximately 2%) were low for both soils. FLM and DMF dissipated more rapidly in RT soil than in NT soil. In FLM-treated RT soil, DMF and TFMPU accumulated more rapidly than in NT as FLM degraded. TFMA dissipated rapidly, primarily as nonextractable residues (approximately 70%, day 42) and volatilization (approximately 16%). For all respective soils in study II, sorption of all four compounds was higher for organic C-enriched RT soils than for CT soils, indicating strong relationships between organic C and FLM and metabolite sorption. For either tillage treatment, the percentage sorption was greater for metabolites (e.g., at lowest initial dosing concentration, TFMPU range, 45-91%; DMF range, 45-90%; and TFMA range, 45-98%) than for FLM (RT soils range, 19-65%). Nonsubstituted amino groups likely facilitated sorption to organic C, with nonsubstituted aniline in TFMA having the greatest affinity. NMR spectra of humic acid extracts from NT and CT Dundee soils indicated similar patterns of humic acid functional groups, but the potential capacity for sorption was greater in NT than in CT. The greater capacity for FLM and metabolite sorption in NT soil helps explain their longer persistence.
在保护性耕作土壤中评估了伏草隆(FLM)及其三种代谢物去甲基伏草隆(DMF)、三氟甲基苯基脲(TFMPU)和三氟甲基苯胺(TFMA)的土壤吸附和消散情况。在研究I中,对免耕(NT)和少耕(RT)区域的表层邓迪粉质壤土分别用14C环标记的FLM或TFMA或未标记的DMF进行处理,孵育34 - 42天,然后进行提取和分析。监测14C标记的FLM或TFMA的矿化和挥发情况。在研究II中,使用来自少耕(RT)和传统耕作(CT)区域的各种土壤进行批量吸附试验(溶质浓度2 - 50 μmol L-1;溶液与土壤比例为2:1;18小时),以确定FLM及其代谢物对不同特性土壤的相对亲和力。两种土壤中FLM(第42天为3%)或TFMA(第34天为4%)的矿化以及FLM的挥发(约2%)都较低。FLM和DMF在RT土壤中的消散速度比在NT土壤中更快。在经FLM处理的RT土壤中,随着FLM降解,DMF和TFMPU的积累速度比在NT土壤中更快。TFMA消散迅速,主要以不可提取的残留物形式存在(第42天约为70%)以及挥发(约16%)。对于研究II中的所有相应土壤,富含有机碳的RT土壤对所有四种化合物的吸附都高于CT土壤,这表明有机碳与FLM及其代谢物吸附之间存在密切关系。对于任何一种耕作处理,代谢物的吸附百分比(例如在最低初始给药浓度下,TFMPU范围为45 - 91%;DMF范围为45 - 90%;TFMA范围为45 - 98%)都高于FLM(RT土壤范围为19 - 65%)。未取代的氨基可能促进了对有机碳的吸附,其中TFMA中的未取代苯胺具有最大的亲和力。NT和CT邓迪土壤腐殖酸提取物的核磁共振光谱表明腐殖酸官能团具有相似的模式,但NT土壤的潜在吸附能力大于CT土壤。NT土壤中对FLM及其代谢物的更大吸附能力有助于解释它们更长的持久性。