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空气中的氯代杀虫剂和天然溴代苯甲醚在三个北欧波罗的海站。

Chlorinated pesticides and natural brominated anisoles in air at three northern Baltic stations.

机构信息

Dept. of Chemistry, Umeå University, SE-901 87 Umeå, Sweden.

Department of Forest Ecology and Management, Swedish University of Agricultural Science (SLU), SE-901 83 Umeå, Sweden.

出版信息

Environ Pollut. 2017 Jun;225:381-389. doi: 10.1016/j.envpol.2017.02.064. Epub 2017 Mar 21.

Abstract

Polyurethane foam (PUF) disk passive samplers were deployed at one inland and two island locations in the Bothnian Bay region of the northern Baltic Sea. Uptake was linear over 81-147 d and a temperature range of -2.6 to 14.2 °C for organochlorine pesticides (OCPs) and current-use pesticides (CUPs) having log K ≥9 at ambient temperatures. Partial saturation of the PUF disks occurred for the more volatile OCPs hexachlorocyclohexanes (HCHs) and hexachlorobenzene (HCB), and for bromoanisoles (BAs), which are products of bromophenols released by natural and anthropogenic sources. Correction for nonlinear uptake of these was made using experimentally measured PUF-air partition coefficients. Passive-derived air concentrations of pesticides were uniform over the bay and agreed within a factor of 2 or better with levels determined by active (pumped) sampling at one of the island stations. Levels of OCPs were similar to those reported at background sites in the European and Canadian Arctic and at monitoring stations in the central Baltic and southern Scandinavia, indicating long-range transport. The insecticide chlorpyrifos was 10 times lower at bay stations than in the Canadian Arctic. Insight to sources and processes was gained by examining compound profiles. Fractions F = α-HCH/(α-HCH + γ-HCH) and F = trans-chlordane/(trans-chlordane + cis-chlordane) at bay stations were higher than in the Norwegian and Finnish Arctic and similar to those at the southern monitoring stations. Volatilization of chlordanes from Baltic seawater may also modify F. Higher F = 2,4,6-TriBA/(2,4,6-TriBA + 2,4-DiBA) distinguished local volatilization from the Baltic Sea versus lower F found at the inland site and reported in air on the Norwegian coast, suggesting westerly transport from the Atlantic across Norway and Sweden.

摘要

聚亚安酯泡沫(PUF)盘式被动采样器在波罗的海北部博特尼亚湾地区的一个内陆和两个岛屿位置进行了部署。对于在环境温度下具有 log K ≥9 的有机氯农药(OCPs)和当前使用的农药(CUPs),在 81-147 d 内和-2.6 至 14.2°C 的温度范围内,吸收是线性的。对于更易挥发的 OCPs 六氯环己烷(HCHs)和六氯苯(HCB)以及溴甲酚(BAs),PUF 盘发生了部分饱和,这些物质是天然和人为来源释放的溴酚的产物。使用实验测量的 PUF-空气分配系数对这些物质的非线性吸收进行了校正。海湾内的农药被动空气浓度是均匀的,与其中一个岛屿站的主动(泵吸)采样所确定的浓度一致,相差不超过 2 倍。OCPs 的水平与欧洲和加拿大北极地区的背景站点以及波罗的海中部和斯堪的纳维亚南部的监测站报告的水平相似,表明存在长距离传输。在海湾站,杀虫剂毒死蜱的水平比加拿大北极地区低 10 倍。通过检查化合物分布,获得了对来源和过程的了解。海湾站的 F = α-HCH/(α-HCH + γ-HCH)和 F = 反式氯丹/(反式氯丹 + 顺式氯丹)分数高于挪威和芬兰北极地区,与南部监测站的分数相似。波罗的海海水中氯丹的挥发也可能改变 F 值。较高的 F = 2,4,6-TriBA/(2,4,6-TriBA + 2,4-DiBA)区分了来自波罗的海的本地挥发与内陆站点和在挪威海岸报道的空气中的较低 F 值,表明从大西洋经挪威和瑞典向西传输。

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