Constraining sulfur incorporation in calcite using inorganic precipitation experiments

Publication date

2024-09-15

Authors

Karancz, Szabina
Uchikawa, Joji
de Nooijer, Lennart J.ISNI 0000000387422339
Wolthers, MariëtteORCID 0000-0003-3908-5622ISNI 0000000074482066
Conner, Kyle A.
Hite, Corinne G.
Zeebe, Richard E.
Sharma, Shiv K.
Reichart, Gert-JanISNI 0000000049622557

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Document Type

Article
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Abstract

The sulfur over calcium ratio (S/Ca) in foraminiferal shells was recently proposed as a new and independent proxy for reconstructing marine inorganic carbon chemistry. This new approach assumes that sulfur is incorporated into CaCO3 predominantly in the form of sulfate (SO42−) through lattice substitution for carbonate ions (CO32–), and that S/Ca thus reflects seawater [CO32–]. Although foraminiferal growth experiments validated this approach, field studies showed controversial results suggesting that the potential impact of [CO32–] may be overwritten by one or more parameters. Hence, to better understand the inorganic processes involved, we here investigate S/Ca values in inorganically precipitated CaCO3 (S/Ca(cc)) grown in solutions of CaCl2 − Na2CO3 − Na2SO4 − B(OH)3 − MgCl2. Experimental results indicate the dependence of sulfate partitioning in CaCO3 on the carbon chemistry via changing pH and suggest that faster precipitation rates increase the partition coefficient for sulfur. The S/Ca ratios of our inorganic calcite samples show positive correlation with modelled [CaSO40](aq), but not with the concentration of free SO42− ions. This challenges the traditional model for sulfate incorporation in calcite and implies that the uptake of sulfate potentially occurs via ion-ion pairs rather than being incorporated as single anions. Based on the [Ca2+] dependence via speciation, we here suggest a critical evaluation of this potential proxy. As sulfate complexation seems to control sulfate uptake in inorganic calcite, application as a proxy using foraminiferal calcite may be limited to periods for which seawater chemistry is well-constrained. As foraminiferal calcite growth is modulated by inward Ca2+ flow to the site of calcification coupled to outward H+ pumping, sulfate incorporation as CaSO40 ion-pair in the foraminifer's shell also provides a mechanistic link for the observed relationship between S/Ca(cc) and [CO32–].

Keywords

Calcite growth experiment, Inorganic carbon chemistry, Ion-pair formation, Proxy, Sulfate incorporation, Geochemistry and Petrology, SDG 14 - Life Below Water

Citation

Karancz, S, Uchikawa, J, de Nooijer, L J, Wolthers, M, Conner, K A, Hite, C G, Zeebe, R E, Sharma, S K & Reichart, G-J 2024, 'Constraining sulfur incorporation in calcite using inorganic precipitation experiments', Geochimica et Cosmochimica Acta, vol. 381, pp. 116-130. https://doi.org/10.1016/j.gca.2024.07.034