Anthropogenic CO2 emissions have perturbed the global carbon cycle and increased atmospheric carbon concentrations to critical levels, making carbon capture and storage (CCS) a key strategy for mitigating climate warming. Natural carbon sequestration has operated continuously in marine environments throughout Earth history. Here, we investigate the growth mechanisms and carbon-sink significance of calcite concretions in the Mesoproterozoic Xiamaling Formation from the Zhaojiashan section and the Zhenzhuquan section in the North China Craton, using petrographic, elemental geochemical and C-O-Re-Os isotopic evidence. The presence of erosional surfaces and local truncation of host-rock laminae suggests that these concretions formed synsedimentarily or during early diagenesis near the sediment-water interface. The δ13C values (−5.05‰ to 1.54‰) of samples, together with δ18O-δ13C relationships, indicate a marine carbonate affinity and suggest that dissolved inorganic carbon was the dominant carbon source. In addition, the concretions display initial 187Os/188Os ratios as low as 0.136, close to the mantle Os end-member, implying a contribution from mantle-derived material during concretion formation. The middle rare earth element and yttrium (MREYs)-enriched patterns and slight positive Ce anomalies further indicate that concretion growth occurred mainly within the Mn- and Fe-reduction zones. We estimate that the calcite-concretion-bearing interval of the Xiamaling Formation sequestered 70.24 Gt C, equivalent to 257.56 Gt CO2, serving as an archive of marine carbon burial in the Mesoproterozoic ocean. Microbially mediated carbonate precipitation may represent an effective carbon immobilization mechanism in marine sediments and has potential implications for the development of subseafloor carbon storage strategies, especially where biocatalysts and/or brine could accelerate seawater CO2 mineral trapping to industrially relevant rates.
Zhang et al. (Mon,) studied this question.
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