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Sources and Seasonal Variations of Per- and Polyfluoroalkyl Substances (PFAS) in Surface Snow in the Arctic
Örebro University, School of Science and Technology. Department of Earth Sciences, University of Oxford, Oxford, U.K.; Department of Arctic Geology, University Centre in Svalbard (UNIS), Svalbard, Norway; NILU, Kjeller, Norway . (Man-Technology-Environment Research Centre (MTM))ORCID iD: 0000-0003-1735-3307
Man-Technology-Environment Research Centre (MTM), Örebro University, Örebro, Sweden; Institute of Environmental Assessment and Water Research (IDAEA-CSIC), Barcelona, Catalonia, Spain.
Örebro University, School of Science and Technology. (Man-Technology-Environment Research Centre (MTM))ORCID iD: 0000-0001-6800-5658
Ice Dynamics and Paleoclimate, British Antarctic Survey, Cambridge, U.K..
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2024 (English)In: Environmental Science and Technology, ISSN 0013-936X, E-ISSN 1520-5851, Vol. 58, no 49, p. 21817-21828Article in journal (Refereed) Published
Abstract [en]

Per- and polyfluoroalkyl substances (PFAS) are persistent anthropogenic contaminants, some of which are toxic and bioaccumulative. Perfluoroalkyl carboxylic acids (PFCAs) and perfluoroalkyl sulfonic acids (PFSAs) can form during the atmospheric degradation of precursors such as fluorotelomer alcohols (FTOHs), N-alkylated perfluoroalkane sulfonamides (FASAs), and hydrofluorocarbons (HFCs). Since PFCAs and PFSAs will readily undergo wet deposition, snow and ice cores are useful for studying PFAS in the Arctic atmosphere. In this study, 36 PFAS were detected in surface snow around the Arctic island of Spitsbergen during January-August 2019 (i.e., 24 h darkness to 24 h daylight), indicating widespread and chemically diverse contamination, including at remote high elevation sites. Local sources meant some PFAS had concentrations in snow up to 54 times higher in Longyearbyen, compared to remote locations. At a remote high elevation ice cap, where PFAS input was from long-range atmospheric processes, the median deposition fluxes of C2-C11 PFCAs, PFOS and HFPO-DA (GenX) were 7.6-71 times higher during 24 h daylight. These PFAS all positively correlated with solar flux. Together this suggests seasonal light is important to enable photochemistry for their atmospheric formation and subsequent deposition in the Arctic. This study provides the first evidence for the possible atmospheric formation of PFOS and GenX from precursors.

Place, publisher, year, edition, pages
American Chemical Society (ACS), 2024. Vol. 58, no 49, p. 21817-21828
Keywords [en]
atmospheric deposition, precursors, hydroxylradicals, trifluoroacetic acid, solar flux, GenX, Svalbard
National Category
Environmental Sciences
Identifiers
URN: urn:nbn:se:oru:diva-117684DOI: 10.1021/acs.est.4c08854ISI: 001363923100001PubMedID: 39588978Scopus ID: 2-s2.0-85210277259OAI: oai:DiVA.org:oru-117684DiVA, id: diva2:1919583
Funder
Swedish Research Council Formas, 2016-01284; 2022-02812Knowledge Foundation, 20160019
Note

The authors gratefully acknowledge financial support from the Swedish Research Council Formas (2016-01284 and Fluoro-Arctic, 2022-02812), the British National Environmental Research Council and the Oxford Doctoral Training Partnership in Environmental Research (NE/L002612/1), the Burdett-Coutts Trust, the Svalbard Science Forum Arctic Field Grant 2019 (RiS ID 11121), the Research Council of Norway (SvalPOP, 196218/S30), the Fram Centre (PharmArctic, 534/75219 and CLEAN) and the Knowledge Foundation (Enforce Research Project, 20160019). FLEXP-ART model simulations are cross-atmospheric research infrastructure services provided by ATMO-ACCESS (EU grant agreement No 101008004). FLEXPART simulations were performed on resources provided by Sigma2-the National Infrastructure for High Performance Computing and Data Storage in Norway. 

Available from: 2024-12-09 Created: 2024-12-09 Last updated: 2025-01-30Bibliographically approved

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Hartz, William F.Yeung, Leo W. Y.Ericson Jogsten, IngridKärrman, Anna

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