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敌草隆、利谷隆及其主要代谢物在原状农田渗漏计中的淋溶情况。

Leaching of Diuron, Linuron and their main metabolites in undisturbed field lysimeters.

作者信息

El Imache Ahde, Dahchour Abdelmalek, Elamrani Btissam, Dousset Sylvie, Pozzonni Fironzo, Guzzella Lucia

机构信息

Faculté des Sciences-Ain Chock, Université Hassan II, Maarif Casablanca, Morocco.

出版信息

J Environ Sci Health B. 2009 Jan;44(1):31-7. doi: 10.1080/03601230802519579.

Abstract

The increasing use of pesticides in Morocco raises the potential risk of groundwater contamination, notably in the Gharb area, which has a shallow groundwater table. Thus, the leaching of two phenyl-ureas, diuron and linuron and their metabolites through undisturbed soil columns was studied under outdoor conditions. The soil chosen is a loamy clay soil, representative of the Gharb agricultural area. After four irrigation events were applied from 31/03/2005 to 15/05/2005, leachates contained higher amounts of linuron (from 0.08% to 6.96% of applied linuron) than diuron (from 0% to 0.27%). The greater mobility of linuron might be related to its higher water solubility (64 mg x L(- 1) compared with 42 mg x L(- 1) for diuron) and smaller adsorption coefficient (K(oc) of 400 L x kg(- 1), compared with 480 L x kg(- 1) for diuron). Concerning their metabolites, greater amounts of, N'-(3,4-dichlorophenyl)-N, (DCPMU) than N'-3,4-dichlorophenylurea (DCPU) were detected N-dimethylurea in the percolates, from 0% to 0.046% and from 0% to 0.008%, respectively. At the end of the monitoring period, more linuron residues than diuron residues were recovered in the soil profiles, 25.02% and 16.41%, respectively. The diuron residues were found mainly in the 0-20 cm soil layer, whereas linuron residues reached the 20-40 cm soil layer. Under such experimental conditions, linuron leaching, and thus its potential to contaminate groundwater, is greater than that of diuron.

摘要

摩洛哥农药使用量的增加提高了地下水污染的潜在风险,尤其是在地下水位较浅的加尔卜地区。因此,研究了在室外条件下,两种苯基脲类除草剂(敌草隆和利谷隆)及其代谢物通过原状土柱的淋溶情况。所选土壤为壤质粘土,代表加尔卜农业区。在2005年3月31日至2005年5月15日进行了四次灌溉后,渗滤液中利谷隆的含量(占施用利谷隆的0.08%至6.96%)高于敌草隆(占0%至0.27%)。利谷隆更强的迁移性可能与其更高的水溶性(64mg/L,而敌草隆为42mg/L)和更小的吸附系数(有机碳吸附系数K(oc)为400L/kg,而敌草隆为480L/kg)有关。关于它们的代谢物,渗滤液中检测到的N'-(3,4-二氯苯基)-N,N-二甲基脲(DCPMU)比N'-3,4-二氯苯基脲(DCPU)更多,分别为0%至0.046%和0%至0.008%。在监测期结束时,土壤剖面中回收的利谷隆残留量比敌草隆残留量更多,分别为25.02%和16.41%。敌草隆残留主要存在于0-20cm土层,而利谷隆残留则到达了20-40cm土层。在这种实验条件下,利谷隆的淋溶及其污染地下水的可能性大于敌草隆。

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