The barite record of the past seawater oxygen isotope composition.
basic_science · Level V
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- Record sourced from PubMed, PMID 40447578.
- Also identified by DOI 10.1038/s41467-025-60309-z and PMC identifier 12125193.
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Abstract
The oxygen isotope composition of seawater (δ<sup>18</sup>O<sub>seawater</sub>) is shaped by high- and low-temperature rock-water interactions, reflecting Earth system's dynamics and evolution. The history of δ<sup>18</sup>O<sub>seawater</sub> remains debated due partly to post-depositional imprints to all current mineral proxies. The oxygen atoms in sulfate minerals are among the most inaccessible to later exchange but often not in isotope equilibrium with ambient water. However, the δ<sup>18</sup>O<sub>sulfate</sub> may reach a plateau or approach equilibrium with the δ<sup>18</sup>O<sub>seawater</sub> as the corresponding δ<sup>34</sup>S<sub>sulfate</sub> increases during microbial sulfate reduction. Here we show 289 paired δ<sup>18</sup>O-δ<sup>34</sup>S values for sedimentary barite spanning six periods of the Phanerozoic Eon. The δ<sup>18</sup>O-δ<sup>34</sup>S trajectories point to variable equilibrium δ<sup>18</sup>O<sub>barite</sub> values for different periods. A ~ 4‰ lower δ<sup>18</sup>O<sub>seawater</sub> value is evident before the Carboniferous than today if assuming the same formation temperature. Utilizing the barite δ<sup>18</sup>O-δ<sup>34</sup>S trajectory approach, we now have a robust proxy to advance the long-debated issue of seawater δ<sup>18</sup>O history.