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添加污水污泥对森林土壤中六嗪酮降解的影响。

Modification to degradation of hexazinone in forest soils amended with sewage sludge.

机构信息

Department of Environmental Sciences, Wenzhou Medical College, University-Town, Wenzhou, Zhejiang, 325035, China.

出版信息

J Hazard Mater. 2012 Jan 15;199-200:96-104. doi: 10.1016/j.jhazmat.2011.10.073. Epub 2011 Nov 3.

Abstract

Influences of one sewage sludge on degradation of hexazinone and formation of its major metabolites were investigated in four forest soils (A, B, C and D), collected in Zhejiang Province, China. In non-amended forest soils, the degradation half-life of hexazinone was 21.4, 30.4, 19.4 and 32.8 days in forest soil A, B, C and D, respectively. Degradation could start in soil A and C without lag period because the two soils had been contaminated by this herbicide for a long time, possibly leading to completion of acclimation period of hexazinone-degrading bacteria. In forest soils amended with sewage sludge, the degradation rate constant increased by 17.3% in soil A, 48.2% in soil B, 8.1% in soil C and 51.6% in soil D, respectively. The higher degradation rates (soil A and C) in non-amended soils accord with the lower rate increase in sewage sludge-amended soils. Under non-sterile conditions, biological mechanism accounted for 51.8-62.4% of hexazinone degradation in four soils. Under sterile conditions, the four soils had the similar chemical degradation capacity for hexazinone. In non-amended soil B, only one metabolite (B) was detected, while two metabolites (B and C) were found in sewage sludge-amended soil B. Similarly situated in agricultural soils, N-demethylation at 6-position of triazine ring, hydroxylation at the 4-positon of cyclohexyl group, and removal of the dimethylamino group with formation of a carbonyl group at 6-position of triazine ring appear to be the principal mechanism involved in hexazinone degradation in sewage sludge-amended forest soils. These data will improve understanding of the actual pollution risk as a result of forest soil fertilization with sewage sludge.

摘要

在中国浙江省采集的四种森林土壤(A、B、C 和 D)中,研究了一种污水污泥对六嗪酮降解及其主要代谢物形成的影响。在未添加的森林土壤中,六嗪酮的降解半衰期分别为 A、B、C 和 D 土壤中的 21.4、30.4、19.4 和 32.8 天。由于这两种土壤长期受到这种除草剂的污染,土壤 A 和 C 中的降解可以在没有滞后期的情况下开始,这可能导致六嗪酮降解菌的适应期完成。在添加污水污泥的森林土壤中,土壤 A 中降解速率常数增加了 17.3%,土壤 B 中增加了 48.2%,土壤 C 中增加了 8.1%,土壤 D 中增加了 51.6%。未添加的土壤中更高的降解率(土壤 A 和 C)与添加污水污泥的土壤中较低的增长率相吻合。在非无菌条件下,生物机制占四种土壤中六嗪酮降解的 51.8-62.4%。在无菌条件下,四种土壤对六嗪酮具有相似的化学降解能力。在未添加的土壤 B 中,仅检测到一种代谢物(B),而在添加污水污泥的土壤 B 中发现了两种代谢物(B 和 C)。同样位于农业土壤中,三嗪环 6 位的 N-脱甲基化、环己基 4 位的羟化以及二甲基氨基的去除和三嗪环 6 位的羰基形成似乎是污水污泥添加森林土壤中六嗪酮降解的主要机制。这些数据将有助于提高对森林土壤施肥用污水污泥导致实际污染风险的认识。

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