North Atlantic Deep Water formation inhibits high Arctic contamination by continental perfluorooctane sulfonate discharges

Perfluorooctane sulfonate (PFOS) is an aliphatic fluorinated compound with eight carbon atoms that is extremely persistent in the environment and can adversely affect human and ecological health. The stability, low reactivity, and high water solubility of PFOS combined with the North American phase-...

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Published in:Global Biogeochemical Cycles
Main Authors: Zhang, Xianming, Zhang, Yanxu, Dassuncao, Clifton, Lohmann, Rainer, Sunderland, Elsie M.
Format: Text
Language:unknown
Published: DigitalCommons@URI 2017
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Online Access:https://digitalcommons.uri.edu/gsofacpubs/176
https://doi.org/10.1002/2017GB005624
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description Perfluorooctane sulfonate (PFOS) is an aliphatic fluorinated compound with eight carbon atoms that is extremely persistent in the environment and can adversely affect human and ecological health. The stability, low reactivity, and high water solubility of PFOS combined with the North American phase-out in production around the year 2000, make it a potentially useful new tracer for ocean circulation. Here we characterize processes affecting the lifetime and accumulation of PFOS in the North Atlantic Ocean and transport to sensitive Arctic regions by developing a 3-D simulation within the MITgcm. The model captures variability in measurements across biogeographical provinces (R2 = 0.90, p=0.01). In 2015, the North Atlantic PFOS reservoir was equivalent to 60% of cumulative inputs from the North American and European continents (1400 Mg). Cumulative inputs to the Arctic accounted for 30% of continental discharges, while the remaining 10% was transported to the tropical Atlantic and other regions. PFOS concentrations declined rapidly after 2002 in the surface mixed-layer (half-life: 1-2 years) but are still increasing below 1000 m depth. During peak production years (1980-2000), plumes of PFOS enriched seawater were transported to the Subarctic in energetic surface ocean currents. However, Atlantic Meridional Overturning Circulation (AMOC) and deep ocean transport returned a substantial fraction of this northward transport (20%, 530 Mg) to southern latitudes and reduced cumulative inputs to the Arctic (730 Mg) by 70%. Weakened AMOC due to climate change is thus likely to increase the magnitude of persistent bioaccumulative pollutants entering the Arctic Ocean.
format Text
author Zhang, Xianming
Zhang, Yanxu
Dassuncao, Clifton
Lohmann, Rainer
Sunderland, Elsie M.
spellingShingle Zhang, Xianming
Zhang, Yanxu
Dassuncao, Clifton
Lohmann, Rainer
Sunderland, Elsie M.
North Atlantic Deep Water formation inhibits high Arctic contamination by continental perfluorooctane sulfonate discharges
author_facet Zhang, Xianming
Zhang, Yanxu
Dassuncao, Clifton
Lohmann, Rainer
Sunderland, Elsie M.
author_sort Zhang, Xianming
title North Atlantic Deep Water formation inhibits high Arctic contamination by continental perfluorooctane sulfonate discharges
title_short North Atlantic Deep Water formation inhibits high Arctic contamination by continental perfluorooctane sulfonate discharges
title_full North Atlantic Deep Water formation inhibits high Arctic contamination by continental perfluorooctane sulfonate discharges
title_fullStr North Atlantic Deep Water formation inhibits high Arctic contamination by continental perfluorooctane sulfonate discharges
title_full_unstemmed North Atlantic Deep Water formation inhibits high Arctic contamination by continental perfluorooctane sulfonate discharges
title_sort north atlantic deep water formation inhibits high arctic contamination by continental perfluorooctane sulfonate discharges
publisher DigitalCommons@URI
publishDate 2017
url https://digitalcommons.uri.edu/gsofacpubs/176
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genre Arctic Ocean
Climate change
North Atlantic Deep Water
North Atlantic
Subarctic
genre_facet Arctic Ocean
Climate change
North Atlantic Deep Water
North Atlantic
Subarctic
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spelling ftunivrhodeislan:oai:digitalcommons.uri.edu:gsofacpubs-1182 2024-09-15T17:54:05+00:00 North Atlantic Deep Water formation inhibits high Arctic contamination by continental perfluorooctane sulfonate discharges Zhang, Xianming Zhang, Yanxu Dassuncao, Clifton Lohmann, Rainer Sunderland, Elsie M. 2017-01-01T08:00:00Z application/pdf https://digitalcommons.uri.edu/gsofacpubs/176 https://doi.org/10.1002/2017GB005624 https://digitalcommons.uri.edu/context/gsofacpubs/article/1182/viewcontent/auto_convert.pdf https://digitalcommons.uri.edu/context/gsofacpubs/article/1182/filename/0/type/additional/viewcontent/Figure1.pdf https://digitalcommons.uri.edu/context/gsofacpubs/article/1182/filename/1/type/additional/viewcontent/Figure2.pdf https://digitalcommons.uri.edu/context/gsofacpubs/article/1182/filename/2/type/additional/viewcontent/Figure3.pdf https://digitalcommons.uri.edu/context/gsofacpubs/article/1182/filename/3/type/additional/viewcontent/Figure4.pdf https://digitalcommons.uri.edu/context/gsofacpubs/article/1182/filename/4/type/additional/viewcontent/Figure5.pdf https://digitalcommons.uri.edu/context/gsofacpubs/article/1182/filename/5/type/additional/viewcontent/Figure6.pdf https://digitalcommons.uri.edu/context/gsofacpubs/article/1182/filename/6/type/additional/viewcontent/Figure7.pdf unknown DigitalCommons@URI https://digitalcommons.uri.edu/gsofacpubs/176 doi:10.1002/2017GB005624 https://digitalcommons.uri.edu/context/gsofacpubs/article/1182/viewcontent/auto_convert.pdf https://digitalcommons.uri.edu/context/gsofacpubs/article/1182/filename/0/type/additional/viewcontent/Figure1.pdf https://digitalcommons.uri.edu/context/gsofacpubs/article/1182/filename/1/type/additional/viewcontent/Figure2.pdf https://digitalcommons.uri.edu/context/gsofacpubs/article/1182/filename/2/type/additional/viewcontent/Figure3.pdf https://digitalcommons.uri.edu/context/gsofacpubs/article/1182/filename/3/type/additional/viewcontent/Figure4.pdf https://digitalcommons.uri.edu/context/gsofacpubs/article/1182/filename/4/type/additional/viewcontent/Figure5.pdf https://digitalcommons.uri.edu/context/gsofacpubs/article/1182/filename/5/type/additional/viewcontent/Figure6.pdf https://digitalcommons.uri.edu/context/gsofacpubs/article/1182/filename/6/type/additional/viewcontent/Figure7.pdf Graduate School of Oceanography Faculty Publications text 2017 ftunivrhodeislan https://doi.org/10.1002/2017GB005624 2024-08-21T00:09:33Z Perfluorooctane sulfonate (PFOS) is an aliphatic fluorinated compound with eight carbon atoms that is extremely persistent in the environment and can adversely affect human and ecological health. The stability, low reactivity, and high water solubility of PFOS combined with the North American phase-out in production around the year 2000, make it a potentially useful new tracer for ocean circulation. Here we characterize processes affecting the lifetime and accumulation of PFOS in the North Atlantic Ocean and transport to sensitive Arctic regions by developing a 3-D simulation within the MITgcm. The model captures variability in measurements across biogeographical provinces (R2 = 0.90, p=0.01). In 2015, the North Atlantic PFOS reservoir was equivalent to 60% of cumulative inputs from the North American and European continents (1400 Mg). Cumulative inputs to the Arctic accounted for 30% of continental discharges, while the remaining 10% was transported to the tropical Atlantic and other regions. PFOS concentrations declined rapidly after 2002 in the surface mixed-layer (half-life: 1-2 years) but are still increasing below 1000 m depth. During peak production years (1980-2000), plumes of PFOS enriched seawater were transported to the Subarctic in energetic surface ocean currents. However, Atlantic Meridional Overturning Circulation (AMOC) and deep ocean transport returned a substantial fraction of this northward transport (20%, 530 Mg) to southern latitudes and reduced cumulative inputs to the Arctic (730 Mg) by 70%. Weakened AMOC due to climate change is thus likely to increase the magnitude of persistent bioaccumulative pollutants entering the Arctic Ocean. Text Arctic Ocean Climate change North Atlantic Deep Water North Atlantic Subarctic University of Rhode Island: DigitalCommons@URI Global Biogeochemical Cycles 31 8 1332 1343