Current estimates of K1* and K2* appear inconsistent with measured CO2 system parameters in cold oceanic regions

Seawater absorption of anthropogenic atmospheric carbon dioxide (CO2) has led to a range of changes in carbonate chemistry, collectively referred to as ocean acidification. Stoichiometric dissociation constants used to convert measured carbonate system variables (pH, pCO2, dissolved inorganic carbon...

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Main Authors: Sulpis, O.J.T., Lauvset, Siv K., Hagens, M.
Other Authors: Geochemistry, General geochemistry
Format: Article in Journal/Newspaper
Language:English
Published: 2020
Subjects:
Online Access:https://dspace.library.uu.nl/handle/1874/409088
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spelling ftunivutrecht:oai:dspace.library.uu.nl:1874/409088 2023-12-03T10:21:01+01:00 Current estimates of K1* and K2* appear inconsistent with measured CO2 system parameters in cold oceanic regions Sulpis, O.J.T. Lauvset, Siv K. Hagens, M. Geochemistry General geochemistry 2020-07-21 application/pdf https://dspace.library.uu.nl/handle/1874/409088 en eng 1812-0784 https://dspace.library.uu.nl/handle/1874/409088 info:eu-repo/semantics/OpenAccess Article 2020 ftunivutrecht 2023-11-08T23:19:23Z Seawater absorption of anthropogenic atmospheric carbon dioxide (CO2) has led to a range of changes in carbonate chemistry, collectively referred to as ocean acidification. Stoichiometric dissociation constants used to convert measured carbonate system variables (pH, pCO2, dissolved inorganic carbon, total alkalinity) into globally comparable parameters are crucial for accurately quantifying these changes. The temperature and salinity coefficients of these constants have generally been experimentally derived under controlled laboratory conditions. Here, we use field measurements of carbonate system variables taken from the Global Ocean Data Analysis Project version 2 and the Surface Ocean CO2 Atlas data products to evaluate the temperature dependence of the carbonic acid stoichiometric dissociation constants. By applying a novel iterative procedure to a large dataset of 948 surface-water, quality-controlled samples where four carbonate system variables were independently measured, we show that the set of equations published by Lueker et al. (2000), currently preferred by the ocean acidification community, overestimates the stoichiometric dissociation constants at temperatures below about 8 ∘C. We apply these newly derived temperature coefficients to high-latitude Argo float and cruise data to quantify the effects on surface-water pCO2 and calcite saturation states. These findings highlight the critical implications of uncertainty in stoichiometric dissociation constants for future projections of ocean acidification in polar regions and the need to improve knowledge of what causes the CO2 system inconsistencies in cold waters. Article in Journal/Newspaper Carbonic acid Ocean acidification Utrecht University Repository
institution Open Polar
collection Utrecht University Repository
op_collection_id ftunivutrecht
language English
description Seawater absorption of anthropogenic atmospheric carbon dioxide (CO2) has led to a range of changes in carbonate chemistry, collectively referred to as ocean acidification. Stoichiometric dissociation constants used to convert measured carbonate system variables (pH, pCO2, dissolved inorganic carbon, total alkalinity) into globally comparable parameters are crucial for accurately quantifying these changes. The temperature and salinity coefficients of these constants have generally been experimentally derived under controlled laboratory conditions. Here, we use field measurements of carbonate system variables taken from the Global Ocean Data Analysis Project version 2 and the Surface Ocean CO2 Atlas data products to evaluate the temperature dependence of the carbonic acid stoichiometric dissociation constants. By applying a novel iterative procedure to a large dataset of 948 surface-water, quality-controlled samples where four carbonate system variables were independently measured, we show that the set of equations published by Lueker et al. (2000), currently preferred by the ocean acidification community, overestimates the stoichiometric dissociation constants at temperatures below about 8 ∘C. We apply these newly derived temperature coefficients to high-latitude Argo float and cruise data to quantify the effects on surface-water pCO2 and calcite saturation states. These findings highlight the critical implications of uncertainty in stoichiometric dissociation constants for future projections of ocean acidification in polar regions and the need to improve knowledge of what causes the CO2 system inconsistencies in cold waters.
author2 Geochemistry
General geochemistry
format Article in Journal/Newspaper
author Sulpis, O.J.T.
Lauvset, Siv K.
Hagens, M.
spellingShingle Sulpis, O.J.T.
Lauvset, Siv K.
Hagens, M.
Current estimates of K1* and K2* appear inconsistent with measured CO2 system parameters in cold oceanic regions
author_facet Sulpis, O.J.T.
Lauvset, Siv K.
Hagens, M.
author_sort Sulpis, O.J.T.
title Current estimates of K1* and K2* appear inconsistent with measured CO2 system parameters in cold oceanic regions
title_short Current estimates of K1* and K2* appear inconsistent with measured CO2 system parameters in cold oceanic regions
title_full Current estimates of K1* and K2* appear inconsistent with measured CO2 system parameters in cold oceanic regions
title_fullStr Current estimates of K1* and K2* appear inconsistent with measured CO2 system parameters in cold oceanic regions
title_full_unstemmed Current estimates of K1* and K2* appear inconsistent with measured CO2 system parameters in cold oceanic regions
title_sort current estimates of k1* and k2* appear inconsistent with measured co2 system parameters in cold oceanic regions
publishDate 2020
url https://dspace.library.uu.nl/handle/1874/409088
genre Carbonic acid
Ocean acidification
genre_facet Carbonic acid
Ocean acidification
op_relation 1812-0784
https://dspace.library.uu.nl/handle/1874/409088
op_rights info:eu-repo/semantics/OpenAccess
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