Mahía J, Martín A, Díaz-Raviña M
Instituto de Investigaciones Agrobiológicas de Galicia CSIC, Avda Vigo s/n, Apartado 122, 15780 Santiago de Compostela, Spain.
Environ Geochem Health. 2008 Apr;30(2):147-52. doi: 10.1007/s10653-008-9149-x. Epub 2008 Feb 2.
Extractable atrazine and its metabolites (hydroxyatrazine, deethylatrazine and deisopropylatrazine) were evaluated in agricultural soils from the temperate humid zone (Galicia, NW Spain) under laboratory conditions. The experiment was performed with five soils with different properties (organic C, soil texture and atrazine application history), both unamended and treated with atrazine at field application rate. Measurements of the atrazine compounds were made at different time intervals (1, 3, 6, 9 and 12 weeks) during a 3-month incubation period. Results showed that only hydroxyatrazine was detected in the extractable fraction of the unamended soils, with values remaining relatively constant throughout the incubation period. Atrazine addition notably increased the concentration of the parent compound and its degradation products; deisopropylatrazine and hydroxyatrazine were the main metabolites detected in the extractable fraction of the treated soils, whereas deethylatrazine was not detected. After 7 days incubation, values of total extractable residues, expressed as percentage of initially added atrazine, ranged from 75 to 86% (25-68% of atrazine, 7-11% of hydroxyatrazine and 9-57% of deisopropylatrazine). The values decreased rapidly during the first 3 weeks of incubation, showing values of 2-8% in soils with higher atrazine application and from 28 to 30% in soils with lower application history. At the end of the incubation, 2-8% of total extractable residues were still detected (0-4% of atrazine, 2-3% of hydroxyatrazine and 0-2% of deisopropylatrazine), indicating a residual effect of atrazine addition. These variations in the extractable fraction indicated that most added atrazine was rapidly degraded, especially in soils with higher application history.
在实验室条件下,对来自温带湿润地区(西班牙西北部加利西亚)的农业土壤中的可提取阿特拉津及其代谢物(羟基阿特拉津、去乙基阿特拉津和去异丙基阿特拉津)进行了评估。该实验使用了五种性质不同(有机碳、土壤质地和阿特拉津施用历史)的土壤,一部分未添加阿特拉津,另一部分以田间施用量添加阿特拉津。在为期3个月的培养期内,在不同时间间隔(1、3、6、9和12周)对阿特拉津化合物进行了测量。结果表明,在未添加阿特拉津的土壤可提取部分中仅检测到羟基阿特拉津,其含量在整个培养期内保持相对稳定。添加阿特拉津显著增加了母体化合物及其降解产物的浓度;在添加阿特拉津的土壤可提取部分中检测到的主要代谢物是去异丙基阿特拉津和羟基阿特拉津,而去乙基阿特拉津未被检测到。培养7天后,以最初添加阿特拉津的百分比表示的总可提取残留量范围为75%至86%(阿特拉津占25% - 68%,羟基阿特拉津占7% - 11%,去异丙基阿特拉津占9% - 57%)。在培养的前3周内,这些值迅速下降,在阿特拉津施用量较高的土壤中降至2% - 8%,在施用历史较短 的土壤中降至28% - 30%。在培养结束时,仍检测到2% - 8%的总可提取残留量(阿特拉津占0% - 4%,羟基阿特拉津占2% - 3%,去异丙基阿特拉津占0% - 2%),表明添加阿特拉津具有残留效应。可提取部分的这些变化表明大多数添加的阿特拉津迅速降解,尤其是在施用历史较长的土壤中。