TY - JOUR

T1 - Substantial incorporation of isotopically heavy reduced U species into marine carbonate sediments

AU - Yuan, Yan

AU - Chen, Tianyu

AU - Zhang, Feifei

AU - Liu, Yuanyuan

AU - Xiong, Guolin

AU - Wei, Guang-Yi

AU - Dahl, Tais W.

AU - Yan, Wen

AU - Ling, Hong-Fei

AU - Cheng, Hai

AU - Shen, Shu-Zhong

N1 - Publisher Copyright: © 2023 Elsevier Ltd

PY - 2023

Y1 - 2023

N2 - The uranium (U) isotope ratio (238U/235U, reported as δ238U) in marine carbonates is an important proxy for reconstructing changes in past oceanic redox conditions, based on the essential assumption that U in carbonates originates from dissolved U(VI) in seawater. However, diagenetic processes may induce the addition of isotopically heavy U(IV) into the carbonates, complicating the application of the U isotope proxy. So far, the valence states of trace amounts of U and its relation with U isotope composition in marine carbonate sediments have not been directly studied. In this study, we have calibrated an ion-exchange chromatographic method to separate U(IV) from U(VI) in geological carbonate samples (e.g., modern and fossil corals, stalagmites, cold seep carbonates) and quantified their contents by mass spectrometry. Our study confirms that modern coral carbonates are faithful archives of U(VI) sourced from seawater. Surprisingly, drill core samples from a modern coral carbonate platform, which bear no sign of alteration inferred from conventional diagenetic proxies (e.g., Mn/Sr), show significant positive correlation between U(IV) fraction and bulk carbonate δ238U, suggesting U(IV) is present in the marine carbonates and drives δ238U toward higher values than that of seawater. We therefore suggest that coupled valence and isotope analyses of U in marine carbonates could provide critical constraints toward reliable reconstruction of marine redox evolution in the Earth's history.

AB - The uranium (U) isotope ratio (238U/235U, reported as δ238U) in marine carbonates is an important proxy for reconstructing changes in past oceanic redox conditions, based on the essential assumption that U in carbonates originates from dissolved U(VI) in seawater. However, diagenetic processes may induce the addition of isotopically heavy U(IV) into the carbonates, complicating the application of the U isotope proxy. So far, the valence states of trace amounts of U and its relation with U isotope composition in marine carbonate sediments have not been directly studied. In this study, we have calibrated an ion-exchange chromatographic method to separate U(IV) from U(VI) in geological carbonate samples (e.g., modern and fossil corals, stalagmites, cold seep carbonates) and quantified their contents by mass spectrometry. Our study confirms that modern coral carbonates are faithful archives of U(VI) sourced from seawater. Surprisingly, drill core samples from a modern coral carbonate platform, which bear no sign of alteration inferred from conventional diagenetic proxies (e.g., Mn/Sr), show significant positive correlation between U(IV) fraction and bulk carbonate δ238U, suggesting U(IV) is present in the marine carbonates and drives δ238U toward higher values than that of seawater. We therefore suggest that coupled valence and isotope analyses of U in marine carbonates could provide critical constraints toward reliable reconstruction of marine redox evolution in the Earth's history.

KW - Carbonates

KW - Isotopes

KW - Redox

KW - Tetravalent uranium

U2 - 10.1016/j.gca.2023.07.023

DO - 10.1016/j.gca.2023.07.023

M3 - Journal article

AN - SCOPUS:85168373398

VL - 358

SP - 27

EP - 37

JO - Geochimica et Cosmochimica Acta. Supplement

JF - Geochimica et Cosmochimica Acta. Supplement

SN - 0046-564X

ER -