No abstract

Gas hydrates represent a huge reservoir of methane in marine sediments, prone to dissociation in response to environmental changes. There is consensus that past events of gas hydrate dissociation in the marine environment mainly occurred during periods of low sea level. Here, we report geochemical data for 2-m-thick layers of seep carbonate collected from a hydrate-bearing drill core from~800-m water depth in the northern South China Sea. The aragonite-rich carbonates reveal positive δ 18 O values, confirming a genetic link with gas hydrate dissociation. Uranium-thorium dating of seep carbonates indicates that gas hydrates at the study site dissociated between 133,300 and 112,700 years BP, hence coinciding with the Last Interglacial (MIS 5e) sea-level highstand. We put forward the concept that a climate-driven increase in temperature was responsible for a period of pronounced gas hydrate dissociation.Plain Language Summary The gas hydrate reservoir is a dynamically changing system extremely susceptible to variations of seafloor temperature and pressure. Therefore, gas hydrate dissociation and subsequent methane seepage frequently occur during times of global climate change, especially during sea-level lowstands with reduced seabed pressure. However, this conclusion was mainly based on dating of seep carbonates sampled from the seabed. As a consequence, one cannot exclude that previous results have been compromised by a sampling bias since seafloor samples are easier to collect. Authigenic seep carbonates from drill cores represent a continuous record of gas hydrate dynamics. Our uranium-thorium dating of seep carbonate from drill cores provides a unique example of the effects of temperature and pressure on the stability of the hydrate system in the Dongsha area, northern South China Sea (SCS), during the last interglacial stage (MIS 5e, about 130,000 years BP). Representing the most similar and most contemporary analog to the current interglacial, the study of a methane release event in the SCS during MIS 5e will shed light on the expected trend of methane release events in the future, while providing insight into the response of low-latitude oceans to climate change.Supporting Information:• Data Set S1

Cold seeps frequently occur at the seafloor along continental margins. The dominant biogeochemical processes at cold seeps are the combined anaerobic oxidation of methane and sulfate reduction, which can significantly impact the global carbon and sulfur cycles. The circulation of methane-rich fluids at margins is highly variable in time and space, and assessing past seepage activity requires the use of specific geochemical markers. In this study, we report multiple sedimentary proxy records for three piston gravity cores (QDN-14A, QDN-14B, and QDN-31) from the Haima seep of the South China Sea (SCS). By combining total organic carbon (TOC), total inorganic carbon (TIC), total nitrogen (TN), total sulfur (TS), acid insoluble carbon and sulfur isotope (δ13Corganic carbon and δ34Sacid-insoluble), and δ34S values of chromium reducibility sulfur (δ34SCRS), as well as carbon isotopes of TIC (δ13CTIC) in sediments, our aim was to provide constraints on methane seepage dynamics in this area. We identified three sediment layers at about 260-300 cm, 380-420 cm and 480-520 cm sediment depth, characterized by particular anomalies of low δ13CTIC values and high TS content, high TS and CRS contents, and high δ34Sacid-insoluble and δ34SCRS values, respectively. On this basis, we propose that these sediment horizons correspond to distinct methane release events preserved in the sediment record. While the exact mechanisms accounting for the presence (or absence) of these particular geochemical signals in the sediment are not known, we propose that they correspond to variations in methane flux and their duration through time. Overall, our results suggest that sedimentary carbon and sulfur and their isotopes are useful tracers for better understanding of methane seepage dynamics over time. Please note that this is an author-produced PDF of an article accepted for publication following peer review. The definitive publisher-authenticated version is available on the publisher Web site.