ALBERT

Description: Mixed methane–sulfide hydrates and carbonates are exposed as a pavement at the seafloor along the crest of one of the accretionary ridges of the Cascadia convergent margin. Vent fields from which methane-charged, low-salinity fluids containing sulfide, ammonia, 4He, and isotopically light CO2 escape are associated with these exposures. They characterize a newly recognized mechanism of dewatering at convergent margins, where freshening of pore waters from hydrate destabilization at depth and free gas drives fluids upward. This process augments the convergence-generated overpressure and leads to local dewatering rates that are much higher than at other margins in the absence of hydrate. Discharge of fluids stimulates benthic oxygen consumption which is orders of magnitude higher than is normally found at comparable ocean depths. The enhanced turnover results from the oxidation of methane, hydrogen sulfide, and ammonia by vent biota. The injection of hydrate methane from the ridge generates a plume hundreds of meters high and several kilometers wide. A large fraction of the methane is oxidized within the water column and generates δ13C anomalies of the dissolved inorganic carbon pool.

Description: Hydrothermal activity in the Central Bransfield Basin revealed an active low-temperature vent field on top of a submarine volcanic structure. A temperature anomaly was detected and the sea floor showed various patches of white silica (opal-A) precipitate exposures and some yellow–brown Fe-oxyhydroxide crusts. Enriched dissolved methane concentrations were encountered. Sediment was near 24°C just after the grab came on deck. No dense population of chemosynthetically based macrofauna known from other hydrothermal venting areas was present, except for pogonophora. The observations suggest that the sedimented hydrothermal field at Hook Ridge is a low-temperature end-member branch from a deeper hydrothermal source.

Description: Authigenic carbonates are intercalated with massive gas hydrates in sediments of the Cascadia margin. The deposits were recovered from the uppermost 50 cm of sediments on the southern summit of the Hydrate Ridge during the RV Sonne cruise SO110. Two carbonate lithologies that differ in chemistry, mineralogy, and fabric make up these deposits. Microcrystalline high-magnesium calcite (14 to 19 mol% MgCO3) and aragonite are present in both semiconsolidated sediments and carbonate-cemented clasts. Aragonite occurs also as a pure phase without sediment impurities. It is formed by precipitation in cavities as botryoidal and isopachous aggregates within pure white, massive gas hydrate. Variations in oxygen isotope values of the carbonates reflect the mineralogical composition and define two end members: a Mg-calcite with δ18O =4.86‰ PDB and an aragonite with δ18O =3.68‰ PDB. On the basis of the ambient bottom-water temperature and accepted equations for oxygen isotope fractionation, we show that the aragonite phase formed in equilibrium with its pore-water environment, and that the Mg-calcite appears to have precipitated from pore fluids enriched in 18O. Oxygen isotope enrichment probably originates from hydrate water released during gas-hydrate destabilization.

Description: Plate collision cuases expulsion of fluids and gases and material turnover in the deep ocean along the global subduction zones. Such cold vents are characterized by mineral precipitates and characteristic assemblages of macro organisms. The latter harbor symbiotic bacteria which utilize the chemically-reduced constituents (CH4 and H2S) of the expelled fluids as their energy and supply their host with food. The interaction between tectonically-induced fluid flow and pumping activity of the vent fauna sets up a shallow recirculation system whose magnitude can be estimated from direct measurements by an in situ vent sampling device (VESP) in connection with tracer studies. The dewatering rates based on the biogeochemical estimates agree surprisingly well with those derived from geophysical estimates.

Description: Oxygen isotope ratios were obtained from authigenic clinoptilolites from Barbados Accretionary Complex, Yamato Basin, and Exmouth Plateau sediments (ODP Sites 672, 797, and 762) in order to investigate the isotopic fractionation between clinoptilolite and pore water at early diagenetic stages and low temperatures. Dehydrated clinoptilolites display isotopic ratios for the zeolite framework (δ18Of) that extend from +18.7‰ to +32.8‰ (vs. SMOW). In combination with associated pore water isotope data, the oxygen isotopic fractionation between clinoptilolite and pore fluids could be assessed in the temperature range from 25°C to 40°C. The resulting fractionation factors of 1.032 at 25°C and 1.027 at 40°C are in good agreement with the theoretically determined oxygen isotope fractionation between clinoptilolite and water. Calculations of isotopic temperatures illustrate that clinoptilolite formation occurred at relatively low temperatures of 17°C to 29°C in Barbados Ridge sediments and at 33°C to 62°C in the Yamato Basin. These data support a low-temperature origin of clinoptilolite and contradict the assumption that elevated temperatures are the main controlling factor for authigenic clinoptilolite formation. Increasing clinoptilolite δ18Of values with depth indicate that clinoptilolites which are now in the deeper parts of the zeolite-bearing intervals had either formed at lower temperatures (17–20°C) or under closed system conditions.

Description: Oxygen isotope analyses of marine diatoms were performed in two independent ways. Stepwise fluorination of hydrous opal-A results in plateau δ180 values representing the isotopic composition of the silica frame oxygen. A method of controlled isotope exchange before silica dehydration also produces reliable results, although the exchangeability of the silica was variable. Consequently, a calibration of the isotope exchange method using the results from stepwise fluorination experiments is very useful (and sometimes essential) in order to select a water vapor of an appropriate isotopic composition to be used for equilibration. Sediment diatom samples Ethmodiscus rex and Thalassiothrix longissima from the Antarctic and the North Atlantic Ocean, respectively, show strong 180 enrichments of 46.8 and 44.1‰, which are caused by large isotope fractionation occurring at the low temperature prevailing during silica-water isotope exchange reactions. However, phytoplankton samples from surface waters of the Norwegian-Greenland Sea and the Bellingshausen Sea (Antarctica) have δ180 values between 30.4 and 35.0‰. Thus, the true silica-water isotopic fractionation is approximately 3 to 10‰ lower than the temperature-dependent silica-water equilibrium published in the literature for sedimentary diatoms. Our results indicate that successive isotope exchange reactions of diatomaceous silica with ambient seawater and/or pore water determine the isotope values of diatoms in sediments.

Description: In situ oxygen fluxes were measured at vent sites in the Aleutian trench at a water depth of almost 5000 m using a TV-guided benthic flux chamber. The flux was 2 orders of magnitude greater than benthic oxygen fluxes in areas unaffected by venting on the continental margin off Alaska. Porewater profiles taken from the surface sediment below a vent site showed high concentrations of sulfide, methane, and ammonia. The reduced carbon and nitrogen compounds are transported to the vent site by fluids expelled from deeper anoxic sediment layers by the forces of plate convergence. The tectonically driven fluid flow was determined from the biochemical turnover in vent communities and was found to be 3.4 ± 0.5 m yr−1. A model was used to quantify the transport of silica, Ca2+, and sulfate via diffusion, advection, and bioirrigation through the surface sediments of a vent site. A nonlocal mixing coefficient of 20–30 yr−1 was determined by fitting the model curves to the measured porewater profiles showing that the transport of solutes within the near-surface sediments and across the sediment-water interface is dominated by the activity of the vent fauna. Sulfate-containing oceanic bottom water and methane-rich vent fluids were mixed below the clam colony to produce sulfide and a CaCO3 precipitate. The vent biota shape their immediate environment and control the sediment-water exchange and the benthic fluxes at vent sites. The oxygen consumption at vent sites is a major sink for oxygen at the study area.

Description: A seismic-reflection survey on the Oregon continental margin conducted in 1989 indicates the widespread presence of gas hydrate beneath the middle and lower slope of this accretionary margin. The seismic signature of gas hydrate, a bottom simulating reflector (BSR) with negative polarity that locally cuts across stratigraphic horizons, is especially well developed beneath Hydrate Ridge. This anomalously shallow accretionary ridge was drilled during Ocean Drilling Program Leg 146 to study fluid venting. In this paper we focus on the seismic data from the southern part of Hydrate Ridge, where little evidence of active venting has previously been reported but where the seismic data indicate a complicated subsurface plumbing system. Apparent disruptions of the BSR beneath the western ridge flank suggest dissociation of gas hydrate in response to slumping. A double BSR beneath the southern crest suggests hydrate destabilization in response to tectonic uplift and folding. On the basis of these and other observations, we propose a qualitative model for the evolution of a hydrate-bearing ridge in an active accretionary complex in which gas hydrate initially stabilizes the sea floor, permitting construction of large ridges that are then eaten away by slumps along their margins. The north-to-south variation in sea-floor venting and subsurface seismic structure along Hydrate Ridge may reflect different stages in the temporal evolution of one of these ridges.