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北极斯瓦尔巴德群岛一个高纬度冰芯中全氟和多氟烷基物质(PFAS)的含量及分布情况

Levels and distribution profiles of Per- and Polyfluoroalkyl Substances (PFAS) in a high Arctic Svalbard ice core.

作者信息

Hartz William F, Björnsdotter Maria K, Yeung Leo W Y, Hodson Andrew, Thomas Elizabeth R, Humby Jack D, Day Chris, Jogsten Ingrid Ericson, Kärrman Anna, Kallenborn Roland

机构信息

Department of Earth Sciences, University of Oxford, South Parks Road, Oxford OX1 3AN, United Kingdom; Department of Arctic Geology, University Centre in Svalbard (UNIS), NO-9171, Longyearbyen, Svalbard, Norway.

Institute of Environmental Assessment and Water Research (IDAEA-CSIC), C/Jordi Girona, 18-26, 08034 Barcelona, Catalonia, Spain; Man-Technology-Environment Research Centre (MTM), Örebro University, SE-701 82 Örebro, Sweden.

出版信息

Sci Total Environ. 2023 May 1;871:161830. doi: 10.1016/j.scitotenv.2023.161830. Epub 2023 Jan 28.

Abstract

Per- and polyfluoroalkyl substances (PFAS) are a group of persistent organic contaminants of which some are toxic and bioaccumulative. Several PFAS can be formed from the atmospheric degradation of precursors such as fluorotelomer alcohols (FTOHs) as well as hydrochlorofluorocarbons (HFCs) and other ozone-depleting chlorofluorocarbon (CFC) replacement compounds. Svalbard ice cores have been shown to provide a valuable record of long-range atmospheric transport of contaminants to the Arctic. This study uses a 12.3 m ice core from the remote Lomonosovfonna ice cap on Svalbard to understand the atmospheric deposition of PFAS in the Arctic. A total of 45 PFAS were targeted, of which 26 were detected, using supercritical fluid chromatography (SFC) tandem mass spectrometry (MS/MS) and ultra-performance liquid chromatography (UPLC) MS/MS. C to C perfluoroalkyl carboxylic acids (PFCAs) were detected continuously in the ice core and their fluxes ranged from 2.5 to 8200 ng m yr (9.51-16,500 pg L). Trifluoroacetic acid (TFA) represented 71 % of the total mass of C - C PFCAs in the ice core and had increasing temporal trends in deposition. The distribution profile of PFCAs suggested that FTOHs were likely the atmospheric precursor to C - C PFCAs, whereas C - C PFCAs had alternative sources, such as HFCs and other CFC replacement compounds. Perfluorooctanesulfonic acid (PFOS) was also widely detected in 82 % of ice core subsections, and its isomer profile (81 % linear) indicated an electrochemical fluorination manufacturing source. Comparisons of PFAS concentrations with a marine aerosol proxy showed that marine aerosols were insignificant for the deposition of PFAS on Lomonosovfonna. Comparisons with a melt proxy showed that TFA and PFOS were mobile during meltwater percolation. This indicates that seasonal snowmelt and runoff from post-industrial accumulation on glaciers could be a significant seasonal source of PFAS to ecosystems in Arctic fjords.

摘要

全氟和多氟烷基物质(PFAS)是一类持久性有机污染物,其中一些具有毒性且会生物累积。几种PFAS可由前体物质的大气降解形成,如氟调聚物醇(FTOH)以及氢氯氟烃(HFC)和其他消耗臭氧层的氯氟烃(CFC)替代化合物。斯瓦尔巴德冰芯已被证明能提供污染物远距离大气传输至北极的宝贵记录。本研究使用来自斯瓦尔巴德偏远的罗蒙诺索夫冰帽的一根12.3米冰芯,以了解北极地区PFAS的大气沉降情况。使用超临界流体色谱(SFC)串联质谱(MS/MS)和超高效液相色谱(UPLC)MS/MS,共针对45种PFAS进行检测,其中26种被检测到。在冰芯中持续检测到碳数为C至C的全氟烷基羧酸(PFCA),其通量范围为2.5至8200纳克/米²·年(9.51 - 16,500皮克/升)。三氟乙酸(TFA)占冰芯中碳数为C至C的PFCA总质量的71%,且其沉积的时间趋势呈上升。PFCA的分布特征表明,FTOH可能是碳数为C至C的PFCA的大气前体,而碳数为C至C的PFCA有其他来源,如HFC和其他CFC替代化合物。全氟辛烷磺酸(PFOS)在82%的冰芯分段中也被广泛检测到,其异构体分布(81%为线性)表明其来源为电化学氟化生产。将PFAS浓度与海洋气溶胶替代物进行比较表明,海洋气溶胶对PFAS在罗蒙诺索夫冰帽上的沉积影响不大。与融水替代物进行比较表明,TFA和PFOS在融水渗透过程中具有流动性。这表明季节性融雪以及冰川上工业后积累的径流可能是北极峡湾生态系统中PFAS的一个重要季节性来源。

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