Book ChapterDOI
Gas Hydrate‐Associated Carbonates and Methane‐Venting at Hydrate Ridge: Classification, Distribution, and Origin of Authigenic Lithologies
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TLDR
In this paper, the authors recognized a direct relationship between gas hydrates and sediment fracturing and the oxygen isotope composition of carbonate lithologies on Hydrate Ridge, and demonstrated carbonate-forming mechanisms of gas hydrate.Abstract:
Hydrate Ridge is part of the accretionary complex at the Cascadia margin and
is an area of widespread carbonate precipitation induced by the expulsion of
methane-rich fluids. All carbonates on Hydrate Ridge are related to the methanecarbon
pool either through anaerobic methanotrophy or through methanogenesis.
Several petrographically distinct lithologies occur in boulder fields or in massive
autochtonous chemoherm complexes which include methane-associated
diagenetic mudstones and venting-induced breccias. The mudstones result from
methane diagenesis in different sediment horizons and geochemical environments
related to very slow methane venting. Cemented bioturbation casts occur
as fragments, complex framework or as clasts together with bivalve shells as part
of intraformational breccias, which are restricted to chemoherm complexes.
Here, fluids ascend from the sub-seafloor and support aragonite-dominated carbonate
precipitation near or at the sediment surface. Voids within mudclast breccias
are either aragonite-rich indicating a formation near the surface at vent sites
or are cemented by dolomite, which indicates formation in deeper parts of the
sediment column. Brecciation is caused by tectonic or slump processes. In addition,
we recognized a direct relationship between gas hydrates and sediment fracturing
as well as the oxygen isotope composition of carbonate lithologies. Such
gas hydrate-associated carbonates either show layered megapores and veins as
relics of the original gas hydrate fabric or consist of aragonite-cemented intraclast
breccias formed by growing and decomposing gas hydrate near the sediment
surface. Both rock fabrics and the enrichment of 180 in high Mg-calcite
demonstrate carbonate-forming mechanisms of gas hydrate.read more
Citations
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Journal ArticleDOI
Biological Considerations in Geotechnical Engineering
TL;DR: In this article, it is shown that microorganisms play an important part on the formation of many fine-grained soils, can alter the behavior of coarse grained soils (including hydraulic conductivity, diffusion and strength), accelerate geochemical reactions by orders of magnitude, promote both weathering and aging, and alter the chemical and mechanical properties of specimens after sampling.
Journal ArticleDOI
Hydrocarbon seep and hydrothermal vent paleoenvironments and paleontology: Past developments and future research directions
TL;DR: The origin of modern vent-seep biota has been attributed to either enhanced accumulation of Paleozoic and Mesozoic relics, or migration of various invertebrate groups into vent and seep environments during the Phanerozoic as discussed by the authors.
Journal ArticleDOI
Fluid and chemical fluxes in and out of sediments hosting methane hydrate deposits on Hydrate Ridge, OR, I: Hydrological provinces
Marta E Torres,James McManus,Douglas E. Hammond,M.A. de Angelis,Katja U Heeschen,S.L. Colbert,Michael D. Tryon,Kevin M. Brown,Erwin Suess +8 more
TL;DR: In this paper, the authors identify three distinct active fluid regimes at Hydrate Ridge, where the bulk of the flow occurs through channels in which gas velocities reach 1 m s−1.
Journal ArticleDOI
Fluid flow, methane fluxes, carbonate precipitation and biogeochemical turnover in gas hydrate-bearing sediments at Hydrate Ridge, Cascadia Margin: numerical modeling and mass balances
Roger Luff,Klaus Wallmann +1 more
TL;DR: A numerical model was applied to investigate and quantify biogeochemical processes and methane turnover in gas hydrate-bearing surface sediments from a cold vent site situated at Hydrate Ridge, an accretionary structure located in the Cascadia Margin subduction zone as mentioned in this paper.
Journal ArticleDOI
Characterization of Specific Membrane Fatty Acids as Chemotaxonomic Markers for Sulfate-Reducing Bacteria Involved in Anaerobic Oxidation of Methane
TL;DR: In this article, the authors extracted membrane fatty acids from a sediment core above marine gas hydrates at Hydrate Ridge, NE Pacific, which are characterized by high sulfate reduction rates driven by the anaerobic oxidation of methane (AOM).
References
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Journal ArticleDOI
A marine microbial consortium apparently mediating anaerobic oxidation of methane
Antje Boetius,Katrin Ravenschlag,Carsten J. Schubert,Dirk Rickert,Friedrich Widdel,Armin Gieseke,Rudolf Amann,Bo Barker Jørgensen,Ursula Witte,Olaf Pfannkuche +9 more
TL;DR: In this article, the authors provide microscopic evidence for a structured consortium of archaea and sulphate-reducing bacteria, which are identified by fluorescence in situ hybridization using specific 16S rRNA-targeted oligonucleotide probes.
OtherDOI
Compilation of stable isotope fractionation factors of geochemical interest
Irving Friedman,James R. O'Neil +1 more
Book ChapterDOI
The Origin and Distribution of Methane in Marine Sediments
TL;DR: Methane has been detected in several cores of rapidly deposited (> 50 m/my) deep sea sediments as discussed by the authors, and the methane originates predominantly from bacterial reduction of CO2, as indicated by complimentary changes with depth in the amount and isotopic composition of redox-linked pore water constituents.
Journal ArticleDOI
An isotopic study of siderites, dolomites and ankerites at high temperatures☆
J Rosenbaum,S.M.F Sheppard +1 more
TL;DR: In this paper, an empirically derived relationship between the chemical composition of a carbonate in the CaCO3-(Ca, Mg)(CO3)2-FeCO3 system and the function 103 In α at 100°C is 103 ∆ α = 8.94XCaCO3 + 9.29XMgCO3+ 8.77XFeCo3 where Xi is the mole percent of component i in the carbonate.
Book
Sedimentary Carbonate Minerals
TL;DR: The role of mineralogy in the Petrology of Sedimentary carbonates is discussed in this paper. But this work is limited to the case of Calcite-Aragonite.