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全氟烷基物质(PFAS)从北极冰川向下游地点的迁移:对来源的影响。

Transport of perfluoroalkyl substances (PFAS) from an arctic glacier to downstream locations: implications for sources.

机构信息

State Key Laboratory in Marine Pollution, Department of Biology and Chemistry, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong SAR, China.

出版信息

Sci Total Environ. 2013 Mar 1;447:46-55. doi: 10.1016/j.scitotenv.2012.10.091. Epub 2013 Jan 31.

Abstract

Perfluoroalkyl substances (PFAS) have been globally detected in various environmental matrices, yet their fate and transport to the Arctic is still unclear, especially for the European Arctic. In this study, concentrations of 17 PFAS were quantified in two ice cores (n=26), surface snow (n=9) and surface water samples (n=14) collected along a spatial gradient in Svalbard, Norway. Concentrations of selected ions (Na(+), SO4(2-), etc.) were also determined for tracing the origins and sources of PFAS. Perfluorobutanoate (PFBA), perfluorooctanoate (PFOA) and perfluorononanoate (PFNA) were the dominant compounds found in ice core samples. Taking PFOA, PFNA and perfluorooctane-sulfonate (PFOS) as examples, higher concentrations were detected in the middle layers of the ice cores representing the period of 1997-2000. Lower concentrations of C8-C12 perfluorocarboxylates (PFCAs) were detected in comparison with concentrations measured previously in an ice core from the Canadian Arctic, indicating that contamination levels in the European Arctic are lower. Average PFAS concentrations were found to be lower in surface snow and melted glacier water samples, while increased concentrations were observed in river water downstream near the coastal area. Perfluorohexanesulfonate (PFHxS) was detected in the downstream locations, but not in the glacier, suggesting existence of local sources of this compound. Long-range atmospheric transport of PFAS was the major deposition pathway for the glaciers, while local sources (e.g., skiing activities) were identified in the downstream locations.

摘要

全氟烷基物质(PFAS)已在各种环境基质中被全球检出,但它们向北极的迁移和归宿仍不清楚,特别是在欧洲北极地区。本研究在挪威斯瓦尔巴群岛的一个空间梯度上采集了 26 个冰芯、9 个雪表面和 14 个地表水样本,定量测定了这 17 种 PFAS 的浓度。还测定了选定离子(Na(+)、SO4(2-)等)的浓度,以追踪 PFAS 的来源和来源。在冰芯样本中发现,全氟丁烷磺酸(PFBA)、全氟辛酸(PFOA)和全氟壬酸(PFNA)是主要化合物。以 PFOA、PFNA 和全氟辛烷磺酸(PFOS)为例,在冰芯的中层中检测到更高的浓度,代表了 1997-2000 年的时期。与以前在加拿大北极的冰芯中测量的浓度相比,C8-C12 全氟羧酸(PFCAs)的浓度较低,这表明欧洲北极的污染水平较低。表面雪和融化的冰川水中的平均 PFAS 浓度较低,而在靠近沿海地区的河流下游水中观察到浓度增加。在下游位置检测到全氟己烷磺酸(PFHxS),但在冰川中未检测到,表明该化合物存在局部来源。长程大气输送是 PFAS 在冰川上的主要沉积途径,而在下游位置则确定了本地来源(例如,滑雪活动)。

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