Methylmercury photodegradation influenced by sea-ice cover in Arctic marine ecosystems

cited By 71 International audience Atmospheric deposition of mercury to remote areas has increased threefold since pre-industrial times. Mercury deposition is particularly pronounced in the Arctic. Following deposition to surface oceans and sea ice, mercury can be converted into methylmercury, a bio...

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Published in:Nature Geoscience
Main Authors: Point, David, Sonke, J.E., Day, R.D., Roseneau, D.G., Hobson, K.A., Vander Pol, S.S., Moors, A.J., Pugh, R.S., Donard, Olivier François Xavier, Becker, P.R.
Other Authors: Laboratoire de Chimie Analytique Bio-Inorganique et Environnement (LCABIE), Université de Pau et des Pays de l'Adour (UPPA)-Centre National de la Recherche Scientifique (CNRS), Institut des sciences analytiques et de physico-chimie pour l'environnement et les materiaux (IPREM), Université de Pau et des Pays de l'Adour (UPPA)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)
Format: Article in Journal/Newspaper
Language:English
Published: HAL CCSD 2011
Subjects:
Online Access:https://hal.science/hal-01590299
https://doi.org/10.1038/ngeo1049
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spelling ftunivpau:oai:HAL:hal-01590299v1 2024-09-15T17:53:56+00:00 Methylmercury photodegradation influenced by sea-ice cover in Arctic marine ecosystems Point, David Sonke, J.E. Day, R.D. Roseneau, D.G. Hobson, K.A. Vander Pol, S.S. Moors, A.J. Pugh, R.S. Donard, Olivier François Xavier Becker, P.R. Laboratoire de Chimie Analytique Bio-Inorganique et Environnement (LCABIE) Université de Pau et des Pays de l'Adour (UPPA)-Centre National de la Recherche Scientifique (CNRS) Institut des sciences analytiques et de physico-chimie pour l'environnement et les materiaux (IPREM) Université de Pau et des Pays de l'Adour (UPPA)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS) 2011 https://hal.science/hal-01590299 https://doi.org/10.1038/ngeo1049 en eng HAL CCSD Nature Publishing Group info:eu-repo/semantics/altIdentifier/doi/10.1038/ngeo1049 hal-01590299 https://hal.science/hal-01590299 doi:10.1038/ngeo1049 ISSN: 1752-0894 Nature Geoscience https://hal.science/hal-01590299 Nature Geoscience, 2011, 4 (3), pp.188-194. ⟨10.1038/ngeo1049⟩ [CHIM.ANAL]Chemical Sciences/Analytical chemistry info:eu-repo/semantics/article Journal articles 2011 ftunivpau https://doi.org/10.1038/ngeo1049 2024-08-11T23:35:13Z cited By 71 International audience Atmospheric deposition of mercury to remote areas has increased threefold since pre-industrial times. Mercury deposition is particularly pronounced in the Arctic. Following deposition to surface oceans and sea ice, mercury can be converted into methylmercury, a biologically accessible form of the toxin, which biomagnifies along the marine food chain. Mass-independent fractionation of mercury isotopes accompanies the photochemical breakdown of methylmercury to less bioavailable forms in surface waters. Here we examine the isotopic composition of mercury in seabird eggs collected from colonies in the North Pacific Ocean, the Bering Sea and the western Arctic Ocean, to determine geographical variations in methylmercury breakdown at northern latitudes. We find evidence for mass-independent fractionation of mercury isotopes. The degree of mass-independent fractionation declines with latitude. Foraging behaviour and geographic variations in mercury sources and solar radiation fluxes were unable to explain the latitudinal gradient. However, mass-independent fractionation was negatively correlated with sea-ice cover. We conclude that sea-ice cover impedes the photochemical breakdown of methylmercury in surface waters, and suggest that further loss of Arctic sea ice this century will accelerate sunlight-induced breakdown of methylmercury in northern surface waters. © 2011 Macmillan Publishers Limited. All rights reserved. Article in Journal/Newspaper Arctic Ocean Bering Sea Sea ice HAL e2s UPPA (Université de Pau et des Pays de l'Adour) Nature Geoscience 4 3 188 194
institution Open Polar
collection HAL e2s UPPA (Université de Pau et des Pays de l'Adour)
op_collection_id ftunivpau
language English
topic [CHIM.ANAL]Chemical Sciences/Analytical chemistry
spellingShingle [CHIM.ANAL]Chemical Sciences/Analytical chemistry
Point, David
Sonke, J.E.
Day, R.D.
Roseneau, D.G.
Hobson, K.A.
Vander Pol, S.S.
Moors, A.J.
Pugh, R.S.
Donard, Olivier François Xavier
Becker, P.R.
Methylmercury photodegradation influenced by sea-ice cover in Arctic marine ecosystems
topic_facet [CHIM.ANAL]Chemical Sciences/Analytical chemistry
description cited By 71 International audience Atmospheric deposition of mercury to remote areas has increased threefold since pre-industrial times. Mercury deposition is particularly pronounced in the Arctic. Following deposition to surface oceans and sea ice, mercury can be converted into methylmercury, a biologically accessible form of the toxin, which biomagnifies along the marine food chain. Mass-independent fractionation of mercury isotopes accompanies the photochemical breakdown of methylmercury to less bioavailable forms in surface waters. Here we examine the isotopic composition of mercury in seabird eggs collected from colonies in the North Pacific Ocean, the Bering Sea and the western Arctic Ocean, to determine geographical variations in methylmercury breakdown at northern latitudes. We find evidence for mass-independent fractionation of mercury isotopes. The degree of mass-independent fractionation declines with latitude. Foraging behaviour and geographic variations in mercury sources and solar radiation fluxes were unable to explain the latitudinal gradient. However, mass-independent fractionation was negatively correlated with sea-ice cover. We conclude that sea-ice cover impedes the photochemical breakdown of methylmercury in surface waters, and suggest that further loss of Arctic sea ice this century will accelerate sunlight-induced breakdown of methylmercury in northern surface waters. © 2011 Macmillan Publishers Limited. All rights reserved.
author2 Laboratoire de Chimie Analytique Bio-Inorganique et Environnement (LCABIE)
Université de Pau et des Pays de l'Adour (UPPA)-Centre National de la Recherche Scientifique (CNRS)
Institut des sciences analytiques et de physico-chimie pour l'environnement et les materiaux (IPREM)
Université de Pau et des Pays de l'Adour (UPPA)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)
format Article in Journal/Newspaper
author Point, David
Sonke, J.E.
Day, R.D.
Roseneau, D.G.
Hobson, K.A.
Vander Pol, S.S.
Moors, A.J.
Pugh, R.S.
Donard, Olivier François Xavier
Becker, P.R.
author_facet Point, David
Sonke, J.E.
Day, R.D.
Roseneau, D.G.
Hobson, K.A.
Vander Pol, S.S.
Moors, A.J.
Pugh, R.S.
Donard, Olivier François Xavier
Becker, P.R.
author_sort Point, David
title Methylmercury photodegradation influenced by sea-ice cover in Arctic marine ecosystems
title_short Methylmercury photodegradation influenced by sea-ice cover in Arctic marine ecosystems
title_full Methylmercury photodegradation influenced by sea-ice cover in Arctic marine ecosystems
title_fullStr Methylmercury photodegradation influenced by sea-ice cover in Arctic marine ecosystems
title_full_unstemmed Methylmercury photodegradation influenced by sea-ice cover in Arctic marine ecosystems
title_sort methylmercury photodegradation influenced by sea-ice cover in arctic marine ecosystems
publisher HAL CCSD
publishDate 2011
url https://hal.science/hal-01590299
https://doi.org/10.1038/ngeo1049
genre Arctic Ocean
Bering Sea
Sea ice
genre_facet Arctic Ocean
Bering Sea
Sea ice
op_source ISSN: 1752-0894
Nature Geoscience
https://hal.science/hal-01590299
Nature Geoscience, 2011, 4 (3), pp.188-194. ⟨10.1038/ngeo1049⟩
op_relation info:eu-repo/semantics/altIdentifier/doi/10.1038/ngeo1049
hal-01590299
https://hal.science/hal-01590299
doi:10.1038/ngeo1049
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container_title Nature Geoscience
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container_issue 3
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