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在马来西亚的湿润热带土壤中,乙酰甲胺磷的降解和矿化动力学。

Degradation and mineralization kinetics of acephate in humid tropic soils of Malaysia.

机构信息

Agriculture Research Centre, Semongok, Department of Agriculture, Sarawak, Borneo Height Road, 93250 Kuching, Sarawak, Malaysia.

出版信息

Chemosphere. 2010 Apr;79(4):434-40. doi: 10.1016/j.chemosphere.2010.01.046. Epub 2010 Feb 26.

Abstract

Acephate is poorly sorbed to soil, thus the risk of leaching to the aquatic environment is high if it is not quickly degraded. The effect of soil moisture, temperature, microbial activity and application rate on acephate degradation has been studied in three Malaysian soils to examine and identify critical variables determining its degradation and mineralization kinetics. First-order kinetics could be used to describe degradation in all cases (r(2)>0.91). Acephate degraded faster in air-dry (t((1/2)) 9-11 d) and field capacity (t((1/2)) 10-16d) soils than in the wet soils (t((1/2)) 32-77 d). The activation energy of degradation was in the range 17-28 kJ mol(-1) and significantly higher for the soil with higher pH and lower clay and iron oxide contents. Soil sterilization caused a 3- to 10-fold decrease in degradation rates compared to non-sterile soils (t((1/2)) 53-116 d) demonstrating that acephate degradation is mainly governed by microbial processes. At 5-fold increase in application rates (25 microg g(-1)), half-life increased slightly (t((1/2)) 13-19 d) or was unaffected. Half-life from acephate mineralization was similar to those from degradation but much longer at the 5-fold increase in acephate application rates (t((1/2)) 41-96 d) demonstrating that degradation of metabolites is rate limiting. Thus, application of acephate should be restricted or avoided during wet seasons with heavy rainfall and flooded soil as in paddy cultivation. Sandy soils with low microbial activity are more prone to acephate leaching than clay soils rich in humic matter.

摘要

乙酰甲胺磷在土壤中吸附性差,如果不能迅速降解,淋溶到水生环境中的风险很高。本研究在马来西亚的三种土壤中,考察了土壤水分、温度、微生物活性和施用量对乙酰甲胺磷降解和矿化动力学的影响,以确定影响其降解和矿化的关键变量。在所有情况下(r(2)>0.91),都可以使用一级动力学来描述降解。在风干(t((1/2)) 9-11 d)和田间持水量(t((1/2)) 10-16d)土壤中,乙酰甲胺磷的降解速度比在潮湿土壤中(t((1/2)) 32-77 d)更快。降解的活化能范围为 17-28 kJ mol(-1),在 pH 值较高、粘土和氧化铁含量较低的土壤中,其值显著较高。土壤灭菌使降解率比非灭菌土壤下降了 3-10 倍(t((1/2)) 53-116 d),这表明乙酰甲胺磷的降解主要受微生物过程的控制。施用量增加 5 倍(25 μg g(-1))时,半衰期略有增加(t((1/2)) 13-19 d)或不受影响。与降解半衰期相似,但在施用量增加 5 倍时(t((1/2)) 41-96 d),乙酰甲胺磷矿化的半衰期要长得多,这表明代谢物的降解是限速步骤。因此,在雨季降雨量较大且土壤被淹没(如在水稻种植中)的情况下,应限制或避免使用乙酰甲胺磷。微生物活性较低的沙质土壤比富含腐殖质的粘性土壤更容易发生乙酰甲胺磷淋溶。

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