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北美和全球表层土壤中全氟烷基物质的调查:分布模式和存在方式。

A North American and global survey of perfluoroalkyl substances in surface soils: Distribution patterns and mode of occurrence.

机构信息

Department of Chemistry, University of Toronto, 80 St. George Street, Toronto, Ontario, M5S 3H6, Canada.

Senior Environmental Employment Program, United States Environmental Protection Agency, 960 College Station Road, Athens, 30605, Georgia.

出版信息

Chemosphere. 2016 Oct;161:333-341. doi: 10.1016/j.chemosphere.2016.06.109. Epub 2016 Jul 18.

Abstract

The distribution of 32 per/polyfluoroalkyl substances (PFASs) in surface soils was determined at 62 locations representing all continents (North America n = 33, Europe n = 10, Asia n = 6, Africa n = 5, Australia n = 4, South America n = 3 and Antarctica n = 1) using ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) systems. Quantifiable levels of perfluoroalkyl carboxylates (PFCAs: PFHxA-PFTeDA) were observed in all samples with total concentrations ranging from 29 to 14,300 pg/g (dry weight), while perfluoroalkane sulfonates (PFSAs: PFHxS, PFOS and PFDS) were detected in all samples but one, ranging from <LOQ-3270 pg/g, confirming the global distribution of PFASs in terrestrial settings. The geometric mean PFCA and PFSA concentrations were observed to be higher in the northern hemisphere (930 and 170 pg/g) compared to the southern hemisphere (190 and 33 pg/g). Perfluorooctanoate (PFOA) and perfluorooctanesulfonate (PFOS) were the most commonly detected analytes at concentrations up to 2670 and 3100 pg/g, respectively. The sum of PFCA homologues of PFOA commonly were roughly twice the concentration of PFOA. The PFCA and PFSA congener profiles were similar amongst most locations, with a few principal-component statistical anomalies suggesting impact from nearby urban and point sources. The ratio of even to odd PFCAs was consistent with the atmospheric oxidation of fluorotelomer-based precursors previously observed in laboratory and environmental studies. Given the soils were collected from locations absent of direct human activity, these results suggest that the atmospheric long-range transport (LRT) of neutral PFASs followed by oxidation and deposition are a significant source of PFCAs and PFSAs to soils.

摘要

采用超高效液相色谱串联质谱(UPLC-MS/MS)系统,在代表各大洲(北美洲 n=33,欧洲 n=10,亚洲 n=6,非洲 n=5,澳大利亚 n=4,南美洲 n=3 和南极洲 n=1)的 62 个地点测定了表层土壤中 32 种全氟和多氟烷基物质(PFASs)的分布情况。所有样品中均检测到可量化水平的全氟烷基羧酸(PFCAs:PFHxA-PFTeDA),总浓度范围为 29 至 14,300 pg/g(干重),而全氟烷磺酸(PFSAs:PFHxS、PFOS 和 PFDS)在除一个样品之外的所有样品中均有检出,浓度范围为 <LOQ-3270 pg/g,证实了 PFASs 在陆地环境中的全球性分布。与南半球(930 和 170 pg/g)相比,北半球(190 和 33 pg/g)的几何平均 PFCAs 和 PFSA 浓度更高。全氟辛烷磺酸(PFOS)和全氟辛烷磺酸(PFOS)是最常见的检测到的分析物,浓度高达 2670 和 3100 pg/g。全氟辛酸(PFOA)及其同系物的总和通常是 PFOA 浓度的两倍左右。大多数地点的 PFCAs 和 PFSA 同系物谱相似,只有少数主成分统计异常表明受到附近城市和点源的影响。偶数到奇数 PFCAs 的比值与先前在实验室和环境研究中观察到的氟调聚物前体的大气氧化一致。鉴于这些土壤是从没有直接人类活动的地点采集的,这些结果表明,中性 PFASs 的大气长程传输(LRT)随后的氧化和沉积是 PFCAs 和 PFSA 进入土壤的重要来源。

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