Molybdenum isotope composition of seep carbonates - Constraints on sediment biogeochemistry in seepage environments

• Published in: Geochimica et Cosmochimica Acta
• Main Authors: Lin, Zhiyong, Sun, Xiaoming, Strauss, Harald, Eroglu, Suemeyya, Boettcher, Michael E., Lu, Yang, Liang, Jinqiang, Li, Jie, Peckmann, Joern
• Format: Report
• Language: English
• Published: PERGAMON-ELSEVIER SCIENCE LTD 2021
• Subjects: Geochemistry & Geophysics; Seep carbonate; Molybdenum isotopic composition; Molybdenum enrichment; Seepage environments; Pyrite; DRIVEN ANAEROBIC OXIDATION; CONTINENTAL-MARGIN SEDIMENTS; GAS HYDRATE OCCURRENCE; MO ISOTOPE; AUTHIGENIC CARBONATES; EUXINIC SEDIMENTS; SULFATE REDUCTION; SULFIDE MINERALS; REDOX CONDITIONS; METHANE HYDRATE; Methane hydrate
• Online Access: http://ir.gig.ac.cn/handle/344008/63265; https://doi.org/10.1016/j.gca.2021.05.038

Methane seepage causes significant changes in the local diagenetic environment and impacts the marine sedimentary cycles of sulfur, carbon, and molybdenum (Mo), which are intimately linked to each other. Molybdenum isotopic compositions were determined for authigenic carbonate nodules and bulk sediments of a 230-m long sediment core collected at a methane seep site in the South China Sea. Authigenic carbonate nodules occur at different sediment depths and display low d13C values around similar to 50% revealing that carbon predominantly derived from biogenic methane. Moreover, seep carbonate nodules are substantially enriched in Mo (Al-normalized enrichment factors MoEF between 27 and 70), and display nearly constant d98Mo values around an average of +1.9% (relative to NIST3134 = +0.25%), close to the Mo isotopic composition of modern seawater (+2.3%). Linear positive correlations between d98Mo values and pyrite sulfur contents and Mo contents were identified for seep carbonate samples. This implies that Mo scavenging into pyrite is likely controlled by hydrogen sulfide availability derived from sulfate-driven anaerobic oxidation of methane (SD-AOM). The essentially constant and high d98Mo values suggest that Mo species were nearly quantitatively incorporated into the authigenic carbonates under highly sulfidic conditions, probably at times when the sulfate-methane transition zones (SMTZ) was situated at shallow sediment depth at times of high seepage activity. In contrast, bulk sediments that exhibit typical marine d13C values close to 0% (versus VPDB), hence devoid of methane-derived seep carbonates, are characterized by low Mo contents (MoEF = similar to 0.9). Their lower d98Mo values mostly ranging from +0.2 to +0.8%, in accord with low Mo contents, likely reflect input of detrital Mo. Bulk sediments bearing seep carbonate nodules display variable d13C values lower than similar to 5% and are characterized by a wide range in Mo contents (MoEF from 1.5 to 45.3) and d98 Mo values (+0.7 to +3.0%). The high d98 Mo values of some sediment samples, relative to the seep carbonate signature, might indicate an additional accumulation of a 98 Mo enriched pool of molybdenum during later SD-AOM at a deeper SMTZ postdating initial seep carbonate formation; such 98Mo enrichment was probably caused by preceding preferential removal of lighter Mo isotopes from pore fluids. Our results indicate that Mo isotope systematics of seep deposits can provide constraints on the dynamics of the biogeochemical cycling of carbon, sulfur, and trace elements in methane seep environments. A potential for authigenic carbonates to archive the Mo isotopic composition of seawater is indicated, but will have to be assessed in future studies.