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International audience; The main Marmara Fault exhibits numerous sites of fluid venting, observed during previous cruises and in particular with ROV VICTOR during the MARMARASCARPS cruise (2002). Long CALYPSO cores were recovered near active vents and at reference sites during the MARMARA-VT cruise (2004), together with echosounder sub-bottom profiles (frequency of 3.5 kHz). We compiled ROV video observations from MARMARASCARPS cruise and show that all known seeps occur in relationship with strike-slip faults, providing pathways for fluid migration. Among the main active sites, a distinction is made between gas seeps and water seeps. At gas seeps, bubble emissions at the seafloor or disturbed echofacies on sounder profiles demonstrate the presence of free methane gas at a shallow depth within the sediment. Most cores displayed gas related expansion, most intense for cores taken within the gas plumes. On the other hand, authigenic carbonate chimneys characterize the water seeps and visible water outflow was observed at two sites (in the Tekirdağ and Central basins). The pore fluid chemistry data show that the water expelled at these sites is brackish water trapped in the sediment during lacustrine times (before 14 cal Kyr BP), in relation with the paleoceanography in the Sea of Marmara. The chimney site in the Tekirdağ basin is located at the outlet of a canyon feeding a buried fan with coarse sandy turbidites. Pore fluid composition profiles indicate that the sand layers channel the brackish fluids laterally from the basin into the fault zone at less than 20 m depth. However, a deeper gas source cannot be excluded.

Two sediment cores retrieved at the northern slope of Sakhalin Island, Sea of Okhotsk, were analyzed for biogenic opal, organic carbon, carbonate, sulfur, major element concentrations, mineral contents, and dissolved substances including nutrients, sulfate, methane, major cations, humic substances, and total alkalinity. Down-core trends in mineral abundance suggest that plagioclase feldspars and other reactive silicate phases (olivine, pyroxene, volcanic ash) are transformed into smectite in the methanogenic sediment sections. The element ratios Na/Al, Mg/Al, and Ca/Al in the solid phase decrease with sediment depth indicating a loss of mobile cations with depth and producing a significant down-core increase in the chemical index of alteration. Pore waters separated from the sediment cores are highly enriched in dissolved magnesium, total alkalinity, humic substances, and boron. The high contents of dissolved organic carbon in the deeper methanogenic sediment sections (50–150 mg dm-3) may promote the dissolution of silicate phases through complexation of Al3+ and other structure-building cations. A non-steady state transport-reaction model was developed and applied to evaluate the down-core trends observed in the solid and dissolved phases. Dissolved Mg and total alkalinity were used to track the in-situ rates of marine silicate weathering since thermodynamic equilibrium calculations showed that these tracers are not affected by ion exchange processes with sediment surfaces. The modeling showed that silicate weathering is limited to the deeper methanogenic sediment section whereas reverse weathering was the dominant process in the overlying surface sediments. Depth-integrated rates of marine silicate weathering in methanogenic sediments derived from the model (81.4–99.2 mmol CO2 m-2 year-1) are lower than the marine weathering rates calculated from the solid phase data (198–245 mmol CO2 m-2 year-1) suggesting a decrease in marine weathering over time. The production of CO2 through reverse weathering in surface sediments (4.22–15.0 mmol CO2 m-2 year-1) is about one order of magnitude smaller than the weathering-induced CO2 consumption in the underlying sediments. The evaluation of pore water data from other continental margin sites shows that silicate weathering is a common process in methanogenic sediments. The global rate of CO2 consumption through marine silicate weathering estimated here as 5–20 Tmol CO2 year-1 is as high as the global rate of continental silicate weathering.

International audience

International audience; Seven sediment cores were taken in the Sea of Okhotsk in a south-north transect along the slope of Sakhalin Island. The retrieved anoxic sediments and pore fluids were analyzed for particulate organic carbon (POC), total nitrogen, total sulfur, dissolved sulfate, sulfide, methane, ammonium, iodide, bromide, calcium, and total alkalinity. A novel method was developed to derive sedimentation rates from a steady-state nitrogen mass balance. Rates of organic matter degradation, sulfate reduction, methane turnover, and carbonate precipitation were derived from the data applying a steady-state transport-reaction model. A good fit to the data set was obtained using the following new rate law for organic matter degradation in anoxic sediments: RPOC = _______________Kc____________ . Kx.POC C (DIC) + C (CH4) + Kc The rate of particulate organic carbon degradation (RPOC) was found to depend on the POC concentration, an age-dependent kinetic constant (kx) and the concentration of dissolved metabolites. Rates are inhibited at high dissolved inorganic carbon (DIC) and dissolved methane (CH4) concentrations. The best fit to the data was obtained applying an inhibition constant KC of 35 ±5 mM. The modeling further showed that bromide and iodide are preferentially released during organic matter degradation in anoxic sediments. Carbonate precipitation is driven by the anaerobic oxidation of methane (AOM) and removes one third of the carbonate alkalinity generated via AOM. The new model of organic matter degradation was further tested and extended to simulate the accumulation of gas hydrates at Blake Ridge. A good fit to the available POC, total nitrogen, dissolved ammonium, bromide, iodide and sulfate data was obtained confirming that the new model can be used to simulate organic matter degradation and methane production over the entire hydrate stability zone (HSZ). The modeling revealed that most of the gas hydrates accumulating in Blake Ridge sediments are neither formed by organic matter degradation within the HSZ nor by dissolved methane transported to the surface by upward fluid flow but rather through the ascent of gas bubbles from deeper sediment layers. The model was further applied to predict rates of hydrate accumulation in Sakhalin slope sediments. It showed that only up to 0.3% of the pore space is occupied by gas hydrates formed via organic matter degradation within the HSZ. Gas bubble ascent may, however, significantly increase the total amount of hydrate in these deposits.

International audience; During the expeditions ANT-XV/2 with R/V Polarstern in 1997/98 and NBP 99-04 with R/V IB N.B. Palmer in 1999, the first samples of hydrothermally influenced sediments of Bransfield Strait were obtained at Hook Ridge, a volcanic edifice in the Central Basin of the Strait. The vent sites are characterized by white siliceous crusts on top of the sediment layer and temperatures measured immediately on deck are up to 48.5°C. The shallow depth of these vent sites (1050 m) particularly controls the chemistry of the pore fluids that are enriched in silica and sulfide and show low pH values. Chloride is depleted up to 20% and the calculated hydrothermal endmember concentration is in the range of 1–84 mM. Since other mechanisms for Cl depletion can be ruled out clearly, the composition of this fluid is attributed to phase separation. While the Cl-depleted fluid is emanating at Hook Ridge, a Cl-enriched fluid can be identified in the adjacent King George Basin. Using a p,x diagram the two corresponding endmember concentrations reveal that the phase separation takes place at subcritical conditions (total depth: ∼2500 m), probably along the whole volcanic edifice.