Isotopically heavy molybdenum burial in oxic pelagic sediments and implications for paleo-redox reconstruction
• Mo is enriched in core-top sediments but is continuously lost after burial. • Mn-mineral transformation leads to the loss of Mo during early diagenesis. • δ 98 Mo of pelagic sediments increases with depth, indicating a heavy Mo sink. • The newfound heavy Mo sink challenges the conventional global Mo budgets. Molybdenum (Mo) concentrations and isotopic signatures (δ 98 Mo) are useful proxies for reconstructing paleo-redox conditions and tracing material cycling in subduction systems. While the Mo isotope geochemistry of diverse geological settings has been extensively studied over the past two decades, the diagenetic effects on Mo behavior in pelagic oxic sediments remain poorly understood. Here, we investigate Mo cycling in Mn-rich pelagic sediments in an 847 cm long sediment core from the deep Pacific Ocean. We observe a systematic downcore decrease in Mo content (28.0 to 6.10 μg/g) together with increasing Mo isotope ratios (δ 98 Mo: −0.52 ‰ to +1.32 ‰). Synchrotron X-ray absorption spectroscopy shows that the average oxidation state of Mn decreases with depth, which is consistent with the transformation of Mn minerals during sediment burial. In contrast to the canonical δ 98 Mo (−0.7 ‰) of Fe-Mn nodules and crusts, the depth-integrated δ 98 Mo value of the Mn-rich sediments is unusually high, likely due to recycling of isotopically light Mo. If our findings are representative for larger areas of the deep ocean, they could potentially challenge the conventional global Mo budget. A revised isotopically heavier oxic Mo sink in the global ocean’s Mo budget would imply a more extensive expansion of oceanic anoxia and/or reduction of the oxic sink during geological periods when seawater had lower δ 98 Mo values.
Authors
- Andrea Koschinsky (ORCID: https://orcid.org/0000-0002-9224-0663)
- Olivier Mathon (ORCID: https://orcid.org/0000-0002-5487-0226)
- Yinan Deng (ORCID: https://orcid.org/0000-0003-4061-9767)
- Florian Scholz (ORCID: https://orcid.org/0000-0001-8653-0448)
- Xiaoming Sun (ORCID: https://orcid.org/0000-0002-0826-345X)
- Alain Manceau (ORCID: https://orcid.org/0000-0003-0845-611X)
- Jianlin Liao (ORCID: https://orcid.org/0000-0001-5504-3487)
- Guoqing Zhao (ORCID: https://orcid.org/0000-0003-3975-0151)
- Zhiyong Lin (ORCID: https://orcid.org/0000-0002-0793-7686)
Institutions
- École Normale Supérieure de Lyon (FR)
- Centre National de la Recherche Scientifique (FR)
- Sun Yat-sen University (CN)
- University of Bremen (DE)
- European Synchrotron Radiation Facility (FR)
- Guangzhou Marine Geological Survey (CN)
- Laboratoire de Chimie (FR)
- Hamburg Institut (Germany) (DE)
- Institute of Earth Environment (CN)
Publication Details
- Journal
- Earth and Planetary Science Letters
- Published
- 2025-06-17
- DOI
- https://doi.org/10.1016/j.epsl.2025.119497
- Citations
- 2
- Primary Topic
- Geochemistry and Elemental Analysis
- Type
- article
- Field-Weighted Citation Impact
- 2.67
Funders
- European Commission
- National Natural Science Foundation of China
- European Research Council
- National Key Research and Development Program of China