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持久性全氟烷基物质和替代化合物 HFPO-DA 通过大西洋门户向北极海洋的传输——北极是汇还是源?

Transport of Legacy Perfluoroalkyl Substances and the Replacement Compound HFPO-DA through the Atlantic Gateway to the Arctic Ocean-Is the Arctic a Sink or a Source?

机构信息

Department for Environmental Chemistry, Helmholtz-Zentrum Geesthacht, Centre for Materials and Coastal Research, 21502 Geesthacht, Germany.

Institute of Inorganic and Applied Chemistry, Universität Hamburg, 20146 Hamburg, Germany.

出版信息

Environ Sci Technol. 2020 Aug 18;54(16):9958-9967. doi: 10.1021/acs.est.0c00228. Epub 2020 Jul 29.

DOI:10.1021/acs.est.0c00228
PMID:32806910
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7733389/
Abstract

The spatial distribution of 29 per- and polyfluoroalkyl substances (PFASs) in seawater was investigated along a sampling transect from Europe to the Arctic and two transects within Fram Strait, located between Greenland and Svalbard, in the summer of 2018. Hexafluoropropylene oxide-dimer acid (HFPO-DA), a replacement compound for perfluorooctanoic acid (PFOA), was detected in Arctic seawater for the first time. This provides evidence for its long-range transport to remote areas. The total PFAS concentration was significantly enriched in the cold, low-salinity surface water exiting the Arctic compared to warmer, higher-salinity water from the North Atlantic entering the Arctic (260 ± 20 pg/L versus 190 ± 10 pg/L). The higher ratio of perfluoroheptanoic acid (PFHpA) to perfluorononanoic acid (PFNA) in outflowing water from the Arctic suggests a higher contribution of atmospheric sources compared to ocean circulation. An east-west cross section of the Fram Strait, which included seven depth profiles, revealed higher PFAS concentrations in the surface water layer than in intermediate waters and a negligible intrusion into deep waters (>1000 m). Mass transport estimates indicated a net inflow of PFASs with ≥8 perfluorinated carbons via the boundary currents and a net outflow of shorter-chain homologues. We hypothesize that this reflects higher contributions from atmospheric sources to the Arctic outflow and a higher retention of the long-chain compounds in melting snow and ice.

摘要

2018 年夏季,沿从欧洲到北极的采样断面以及格陵兰和斯瓦尔巴群岛之间的弗拉姆海峡的两条断面,调查了海水中 29 种全氟和多氟烷基物质(PFAS)的空间分布。六氟环氧丙烷二聚酸(HFPO-DA)是全氟辛酸(PFOA)的替代品,这是首次在北极海水中检测到这种物质。这为其长距离传输到偏远地区提供了证据。与进入北极的北大西洋较温暖、高盐度的水(190±10 pg/L)相比,北极冷低盐表层水中的总 PFAS 浓度明显更高(260±20 pg/L)。从北极流出的水中的全氟庚酸(PFHpA)与全氟壬酸(PFNA)的比例较高,表明与海洋环流相比,大气源的贡献更高。弗拉姆海峡的东西向断面包括 7 个深度剖面,显示表层水中的 PFAS 浓度高于中层水,对深层水(>1000 m)的影响可以忽略不计。物质传输估算表明,边界流以≥8 个全氟化碳的净通量输入 PFASs,而较短链同系物的净通量输出。我们假设这反映了大气源对北极流出物的更高贡献,以及长链化合物在融雪中的更高保留和在冰中的更高保留。

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