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  • 1
    Publication Date: 2019-10-24
    Description: The upward migration of gas through marine sediments typically manifests itself as gas chimneys or pipes in seismic images and can lead to the formation of cold seeps. Gas seepage is often linked to morphological features like seabed domes, pockmarks, and carbonate build-ups. In this context, sediment doming is discussed to be a precursor of pockmark formation. Here, we present parametric echosounder, sidescan sonar, and two-dimensional seismic data from Opouawe Bank, offshore New Zealand, providing field evidence for sediment doming. Geomechanical quantification of the stresses required for doming show that the calculated gas column heights are geologically feasible and consistent with the observed geophysical data. The progression from channeled gas flow to gas trapping results in overpressure build-up in the shallow sediment. Our results suggest that by breaching of domed seafloor sediments a new seep site can develop, but contrary to ongoing discussion this does not necessarily lead to the formation of pockmarks.
    Type: Article , PeerReviewed , info:eu-repo/semantics/article
    Format: text
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  • 2
    Publication Date: 2019-10-24
    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.
    Type: Article , PeerReviewed
    Format: text
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