Calcium Carbonate Hexahydrate (Ikaite): History of Mineral Formation as Recorded by Stable Isotopes

Calcium carbonate hexahydrate (ikaite) is a rare mineral that forms as metastable species in the organic-carbon-rich sediments of the King George Basin, Bransfield Strait, Antarctica, as a consequence of early diagenetic decomposition of organic matter under cold water (−1.4 °C) and high pressure (2...

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Published in:Minerals
Main Authors: Whiticar, Michael J., Suess, Erwin, Wefer, Gerold, Müller, Peter J.
Format: Article in Journal/Newspaper
Language:English
Published: MDPI 2022
Subjects:
Online Access:https://oceanrep.geomar.de/id/eprint/57561/
https://oceanrep.geomar.de/id/eprint/57561/1/minerals-12-01627-v2.pdf
https://doi.org/10.3390/min12121627
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spelling ftoceanrep:oai:oceanrep.geomar.de:57561 2024-02-11T09:56:59+01:00 Calcium Carbonate Hexahydrate (Ikaite): History of Mineral Formation as Recorded by Stable Isotopes Whiticar, Michael J. Suess, Erwin Wefer, Gerold Müller, Peter J. 2022-12-17 text https://oceanrep.geomar.de/id/eprint/57561/ https://oceanrep.geomar.de/id/eprint/57561/1/minerals-12-01627-v2.pdf https://doi.org/10.3390/min12121627 en eng MDPI https://oceanrep.geomar.de/id/eprint/57561/1/minerals-12-01627-v2.pdf Whiticar, M. J., Suess, E., Wefer, G. and Müller, P. J. (2022) Calcium Carbonate Hexahydrate (Ikaite): History of Mineral Formation as Recorded by Stable Isotopes. Open Access Minerals, 12 . Art.Nr. 1627. DOI 10.3390/min12121627 <https://doi.org/10.3390/min12121627>. doi:10.3390/min12121627 cc_by_4.0 info:eu-repo/semantics/openAccess Article PeerReviewed 2022 ftoceanrep https://doi.org/10.3390/min12121627 2024-01-15T00:26:28Z Calcium carbonate hexahydrate (ikaite) is a rare mineral that forms as metastable species in the organic-carbon-rich sediments of the King George Basin, Bransfield Strait, Antarctica, as a consequence of early diagenetic decomposition of organic matter under cold water (−1.4 °C) and high pressure (200 bar) conditions. Large crystals grow in the sediment immediately below the diagenetic transition between microbial sulfate reduction and methanogenesis at ~320 cm below sea floor (bsf). This process is reflected in the dissolved sulfate, total carbon dioxide, and methane concentrations, as well as in the carbon, hydrogen, and oxygen isotope chemistries of the interstitial fluids and dissolved gases of the host sediment. The ikaite crystal faithfully records in its zonal structure the changing carbon isotope ratio of the total dissolved carbon dioxide pool as it gradually diminishes during methanogenesis (δ13Cikaite = −17.5 to −21.4‰). These changes in the crystal’s host environment follow general Rayleigh carbon isotope fractionation. The oxygen isotopes of the ikaite carbonate (δ18Oikaite = 1.46 to 4.45‰) also show a strong zonal distribution, unrelated to temperature of formation, but perhaps controlled by the degree of recrystallization of ikaite to calcite. The crystal water of the ikaite is depleted 11‰ in 2H/1H (VSMOW) relative to the coexisting interstitial water, which is in excellent agreement with the isotope fractionation of other hydrated minerals. In addition to the in situ temperature and pressure, nucleation of the ikaite crystals in the Bransfield Basin sediments may be induced by the high alkalinity, high phosphate concentrations, and dissolved organic compounds. Intense microbial metabolism generates such compounds; of these, aspartic acid and glutamic acid may play an important role, as they do in biological and extracellular carbonate mineral precipitation. All indications are that low temperatures (such as of polar environments), high calcium carbonate supersaturation caused by interstitial ... Article in Journal/Newspaper Antarc* Antarctica Bransfield Strait OceanRep (GEOMAR Helmholtz Centre für Ocean Research Kiel) Bransfield Strait Minerals 12 12 1627
institution Open Polar
collection OceanRep (GEOMAR Helmholtz Centre für Ocean Research Kiel)
op_collection_id ftoceanrep
language English
description Calcium carbonate hexahydrate (ikaite) is a rare mineral that forms as metastable species in the organic-carbon-rich sediments of the King George Basin, Bransfield Strait, Antarctica, as a consequence of early diagenetic decomposition of organic matter under cold water (−1.4 °C) and high pressure (200 bar) conditions. Large crystals grow in the sediment immediately below the diagenetic transition between microbial sulfate reduction and methanogenesis at ~320 cm below sea floor (bsf). This process is reflected in the dissolved sulfate, total carbon dioxide, and methane concentrations, as well as in the carbon, hydrogen, and oxygen isotope chemistries of the interstitial fluids and dissolved gases of the host sediment. The ikaite crystal faithfully records in its zonal structure the changing carbon isotope ratio of the total dissolved carbon dioxide pool as it gradually diminishes during methanogenesis (δ13Cikaite = −17.5 to −21.4‰). These changes in the crystal’s host environment follow general Rayleigh carbon isotope fractionation. The oxygen isotopes of the ikaite carbonate (δ18Oikaite = 1.46 to 4.45‰) also show a strong zonal distribution, unrelated to temperature of formation, but perhaps controlled by the degree of recrystallization of ikaite to calcite. The crystal water of the ikaite is depleted 11‰ in 2H/1H (VSMOW) relative to the coexisting interstitial water, which is in excellent agreement with the isotope fractionation of other hydrated minerals. In addition to the in situ temperature and pressure, nucleation of the ikaite crystals in the Bransfield Basin sediments may be induced by the high alkalinity, high phosphate concentrations, and dissolved organic compounds. Intense microbial metabolism generates such compounds; of these, aspartic acid and glutamic acid may play an important role, as they do in biological and extracellular carbonate mineral precipitation. All indications are that low temperatures (such as of polar environments), high calcium carbonate supersaturation caused by interstitial ...
format Article in Journal/Newspaper
author Whiticar, Michael J.
Suess, Erwin
Wefer, Gerold
Müller, Peter J.
spellingShingle Whiticar, Michael J.
Suess, Erwin
Wefer, Gerold
Müller, Peter J.
Calcium Carbonate Hexahydrate (Ikaite): History of Mineral Formation as Recorded by Stable Isotopes
author_facet Whiticar, Michael J.
Suess, Erwin
Wefer, Gerold
Müller, Peter J.
author_sort Whiticar, Michael J.
title Calcium Carbonate Hexahydrate (Ikaite): History of Mineral Formation as Recorded by Stable Isotopes
title_short Calcium Carbonate Hexahydrate (Ikaite): History of Mineral Formation as Recorded by Stable Isotopes
title_full Calcium Carbonate Hexahydrate (Ikaite): History of Mineral Formation as Recorded by Stable Isotopes
title_fullStr Calcium Carbonate Hexahydrate (Ikaite): History of Mineral Formation as Recorded by Stable Isotopes
title_full_unstemmed Calcium Carbonate Hexahydrate (Ikaite): History of Mineral Formation as Recorded by Stable Isotopes
title_sort calcium carbonate hexahydrate (ikaite): history of mineral formation as recorded by stable isotopes
publisher MDPI
publishDate 2022
url https://oceanrep.geomar.de/id/eprint/57561/
https://oceanrep.geomar.de/id/eprint/57561/1/minerals-12-01627-v2.pdf
https://doi.org/10.3390/min12121627
geographic Bransfield Strait
geographic_facet Bransfield Strait
genre Antarc*
Antarctica
Bransfield Strait
genre_facet Antarc*
Antarctica
Bransfield Strait
op_relation https://oceanrep.geomar.de/id/eprint/57561/1/minerals-12-01627-v2.pdf
Whiticar, M. J., Suess, E., Wefer, G. and Müller, P. J. (2022) Calcium Carbonate Hexahydrate (Ikaite): History of Mineral Formation as Recorded by Stable Isotopes. Open Access Minerals, 12 . Art.Nr. 1627. DOI 10.3390/min12121627 <https://doi.org/10.3390/min12121627>.
doi:10.3390/min12121627
op_rights cc_by_4.0
info:eu-repo/semantics/openAccess
op_doi https://doi.org/10.3390/min12121627
container_title Minerals
container_volume 12
container_issue 12
container_start_page 1627
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