Reconsidering the role of carbonate ion concentration in calcification by marine organisms

Marine organisms precipitate 0.5–2.0 Gt of carbon as calcium carbonate (CaCO 3 ) every year with a profound impact on global biogeochemical element cycles. Biotic calcification relies on calcium ions (Ca 2+ ) and usually on bicarbonate ions (HCO 3 − ) as CaCO 3 substrates and can be inhibited by hig...

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Published in:Biogeosciences
Main Author: Bach, L. T.
Format: Text
Language:English
Published: 2018
Subjects:
Online Access:https://doi.org/10.5194/bg-12-4939-2015
https://www.biogeosciences.net/12/4939/2015/
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spelling ftcopernicus:oai:publications.copernicus.org:bg29837 2023-05-15T17:50:48+02:00 Reconsidering the role of carbonate ion concentration in calcification by marine organisms Bach, L. T. 2018-09-27 application/pdf https://doi.org/10.5194/bg-12-4939-2015 https://www.biogeosciences.net/12/4939/2015/ eng eng doi:10.5194/bg-12-4939-2015 https://www.biogeosciences.net/12/4939/2015/ eISSN: 1726-4189 Text 2018 ftcopernicus https://doi.org/10.5194/bg-12-4939-2015 2019-12-24T09:53:12Z Marine organisms precipitate 0.5–2.0 Gt of carbon as calcium carbonate (CaCO 3 ) every year with a profound impact on global biogeochemical element cycles. Biotic calcification relies on calcium ions (Ca 2+ ) and usually on bicarbonate ions (HCO 3 − ) as CaCO 3 substrates and can be inhibited by high proton (H + ) concentrations. The seawater concentration of carbonate ions (CO 3 2− ) and the CO 3 2− -dependent CaCO 3 saturation state (Ω CaCO 3 ) seem to be irrelevant in this production process. Nevertheless, calcification rates and the success of calcifying organisms in the oceans often correlate surprisingly well with these two carbonate system parameters. This study addresses this dilemma through the rearrangement of carbonate system equations which revealed an important proportionality between [CO 3 2− ] or Ω CaCO 3 and the ratio of [HCO 3 − ] to [H + ]. Due to this proportionality, calcification rates will always correlate as well with [HCO 3 − ] / [H + ] as they do with [CO 3 2− ] or Ω CaCO 3 when temperature, salinity, and pressure are constant. Hence, [CO 3 2− ] and Ω CaCO 3 may simply be very good proxies for the control by [HCO 3 − ] / [H + ], where [HCO 3 − ] serves as the inorganic carbon substrate and [H + ] functions as a calcification inhibitor. If the "substrate–inhibitor ratio" (i.e., [HCO 3 − ] / [H + ]) rather than [CO 3 2− ] or Ω CaCO 3 controls biotic CaCO 3 formation, then some of the most common paradigms in ocean acidification research need to be reviewed. For example, the absence of a latitudinal gradient in [HCO 3 − ] / [H + ] in contrast to [CO 3 2− ] and Ω CaCO 3 could modify the common assumption that high latitudes are affected most severely by ocean acidification. Text Ocean acidification Copernicus Publications: E-Journals Biogeosciences 12 16 4939 4951
institution Open Polar
collection Copernicus Publications: E-Journals
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language English
description Marine organisms precipitate 0.5–2.0 Gt of carbon as calcium carbonate (CaCO 3 ) every year with a profound impact on global biogeochemical element cycles. Biotic calcification relies on calcium ions (Ca 2+ ) and usually on bicarbonate ions (HCO 3 − ) as CaCO 3 substrates and can be inhibited by high proton (H + ) concentrations. The seawater concentration of carbonate ions (CO 3 2− ) and the CO 3 2− -dependent CaCO 3 saturation state (Ω CaCO 3 ) seem to be irrelevant in this production process. Nevertheless, calcification rates and the success of calcifying organisms in the oceans often correlate surprisingly well with these two carbonate system parameters. This study addresses this dilemma through the rearrangement of carbonate system equations which revealed an important proportionality between [CO 3 2− ] or Ω CaCO 3 and the ratio of [HCO 3 − ] to [H + ]. Due to this proportionality, calcification rates will always correlate as well with [HCO 3 − ] / [H + ] as they do with [CO 3 2− ] or Ω CaCO 3 when temperature, salinity, and pressure are constant. Hence, [CO 3 2− ] and Ω CaCO 3 may simply be very good proxies for the control by [HCO 3 − ] / [H + ], where [HCO 3 − ] serves as the inorganic carbon substrate and [H + ] functions as a calcification inhibitor. If the "substrate–inhibitor ratio" (i.e., [HCO 3 − ] / [H + ]) rather than [CO 3 2− ] or Ω CaCO 3 controls biotic CaCO 3 formation, then some of the most common paradigms in ocean acidification research need to be reviewed. For example, the absence of a latitudinal gradient in [HCO 3 − ] / [H + ] in contrast to [CO 3 2− ] and Ω CaCO 3 could modify the common assumption that high latitudes are affected most severely by ocean acidification.
format Text
author Bach, L. T.
spellingShingle Bach, L. T.
Reconsidering the role of carbonate ion concentration in calcification by marine organisms
author_facet Bach, L. T.
author_sort Bach, L. T.
title Reconsidering the role of carbonate ion concentration in calcification by marine organisms
title_short Reconsidering the role of carbonate ion concentration in calcification by marine organisms
title_full Reconsidering the role of carbonate ion concentration in calcification by marine organisms
title_fullStr Reconsidering the role of carbonate ion concentration in calcification by marine organisms
title_full_unstemmed Reconsidering the role of carbonate ion concentration in calcification by marine organisms
title_sort reconsidering the role of carbonate ion concentration in calcification by marine organisms
publishDate 2018
url https://doi.org/10.5194/bg-12-4939-2015
https://www.biogeosciences.net/12/4939/2015/
genre Ocean acidification
genre_facet Ocean acidification
op_source eISSN: 1726-4189
op_relation doi:10.5194/bg-12-4939-2015
https://www.biogeosciences.net/12/4939/2015/
op_doi https://doi.org/10.5194/bg-12-4939-2015
container_title Biogeosciences
container_volume 12
container_issue 16
container_start_page 4939
op_container_end_page 4951
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