CSIRO Land and Water, Private Mail Bag 2, Glen Osmond 5064, Australia.
J Environ Manage. 2010 Dec;91(12):2649-56. doi: 10.1016/j.jenvman.2010.07.037. Epub 2010 Aug 19.
We studied the leaching and dissipation of atrazine (2-chloro-4-ethylamino-6-isopropylamino-1, 3, 5-s-triazine) and its two principal metabolites (desethylatrazine and desisopropylatrazine) for more than two years through soil profiles at five forestry sites across Australia (representing subtropical, temperate and Mediterranean climatic conditions with rainfall ranging from 780 to 1536 mm yr(-1)). Following atrazine applications at local label rates, soil cores were collected at regular intervals (up to depths of 90-150 cm), and the residues of the three compounds in soil were analysed in composite samples using liquid chromatography. Bromide was applied simultaneously with atrazine to follow the movement of the soil water. While bromide ion rapidly leached through the entire profile, in most cases the bulk of atrazine, desethylatrazine and desisopropylatrazine remained in the top 45 cm of the soil profile. However, a small fraction of residue moved deeper into the soil profile and at a subtropical site (Toolara) trace levels (ng L(-1)) of atrazine and one of its metabolites (DEA) were detected in perched groundwater located at a depth of 1.8 m. Data on the total residues of atrazine in soil profiles from all sites except the Tasmanian site fitted a first-order decay model. The half-life of atrazine in surface soils at the subtropical sites (Toolara and Imbil) ranged from 11 to 21 days. Four separate applications of atrazine at Toolara resulted in a narrow range of half-lives (16 ± 3.6 days), confirming relatively rapid dissipation of atrazine under subtropical conditions (Queensland). In contrast, a prominent biphasic pattern of initial rapid loss followed by very slow phase of degradation of atrazine was observed under the colder temperate climate of Highclere (Tasmania). The data showed that while its 50% (DT(50)) loss occurred relatively rapidly (36 days), more than 10% of herbicide residue was still detectable in the profile even a year after application (DT(90) = 375 days). The rate of dissipation of atrazine at warm subtropical Queensland sites (Imbil and Toolara) was 2-3 times faster than sites located in colder climate of Tasmania. The marked contrast in DT(50) values between subtropical and temperate sites suggest that climatic conditions (soil temperature) is one of the key factors affecting atrazine dissipation. At the Tasmanian site, the combination of leaching of the herbicide in subsoil and slower microbial activity at cooler temperatures would have caused a longer persistence of atrazine.
我们在澳大利亚五个林业站点的土壤剖面中研究了莠去津(2-氯-4-乙氨基-6-异丙氨基-1,3,5-三嗪)及其两种主要代谢物(去乙基莠去津和去异丙基莠去津)的淋溶和消解,历时两年多。在以当地标签用量施用莠去津后,定期采集土壤芯(最多至 90-150 厘米深),并在复合样本中使用液相色谱法分析土壤中三种化合物的残留。溴化物与莠去津同时施用,以跟踪土壤水分的运移。溴化物离子迅速淋溶通过整个剖面,而莠去津、去乙基莠去津和去异丙基莠去津的大部分仍留在土壤剖面的前 45 厘米。然而,一小部分残留物质移动到土壤剖面的更深层,在亚热带地区(Toolara),在深度为 1.8 米的地下水蓄水层中检测到莠去津及其一种代谢物(DEA)的痕量水平(ng L(-1))。除塔斯马尼亚站点外,所有站点土壤剖面中莠去津的总残留数据均符合一级衰减模型。亚热带地区(Toolara 和 Imbil)表层土壤中莠去津的半衰期范围为 11-21 天。在 Toolara 进行了四次单独的莠去津施药,半衰期范围较窄(16±3.6 天),证实了亚热带条件(昆士兰州)下莠去津的快速消解。相比之下,在寒冷的温带气候(塔斯马尼亚州的 Highclere)下,观察到莠去津初始快速损失的双峰模式,随后是非常缓慢的降解阶段。数据表明,虽然其 50%(DT(50))损失相对较快(36 天),但施药一年后,土壤剖面中仍能检测到超过 10%的除草剂残留(DT(90) = 375 天)。温暖的亚热带昆士兰州站点(Imbil 和 Toolara)莠去津的消解速度是寒冷的塔斯马尼亚气候站点的 2-3 倍。亚热带和温带站点之间 DT(50)值的显著差异表明,气候条件(土壤温度)是影响莠去津消解的关键因素之一。在塔斯马尼亚站点,除草剂在亚土层中的淋溶和较低温度下微生物活性较慢的组合将导致莠去津的更长持久性。