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  • 2010-2014  (22)
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  • 1
    Keywords: Hochschulschrift
    Description / Table of Contents: Calcium carbonates (CaCO32-­‐) belong to the most common mineral groups within the marine realm. In this thesis interactions between marine microbes and carbonate stability are investigated in depth. Microbial biofilms are analyzed at high resolution regarding their functions in element and isotopic fractionation. In addition, calcite dissolution experiments were carried out to quantify the effect of aerobic methane oxidizing bacteria. Carbonate precipitation rates in marine sediments often serve as a fitting parameter for numerical modeling approaches to constrain. 45Ca and 14C-bicarbonate incubation experiments were carried out to quantify ongoing calcification in natural sediment slurries. During a research cruise rates of anaerobic methane oxidation and sulfate reduction were determined for the first time using radiotracers. The obtained rates were combined with carbonate isotopic signatures to elucidate local variations of fluid advection.
    Type of Medium: Online Resource
    Pages: Online-Ressource
    DDC: 577.7144
    Language: English
    Note: Kiel, Univ., Diss., 2012
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  • 2
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    PANGAEA
    In:  Supplement to: Berndt, Christian; Feseker, Tomas; Treude, Tina; Krastel, Sebastian; Liebetrau, Volker; Niemann, Helge; Bertics, Victoria J; Dumke, Ines; Dünnbier, Karolin; Ferre, Benedicte; Graves, Carolyn; Gross, Felix; Hissmann, Karen; Hühnerbach, Veit; Krause, Stefan; Lieser, Kathrin; Schauer, Jürgen; Steinle, Lea (2014): Temporal constraints on hydrate-controlled methane seepage off Svalbard. Published Online January 2 2014, Science, https://doi.org/10.1126/science.1246298
    Publication Date: 2023-03-03
    Description: Methane hydrate is an ice-like substance that is stable at high-pressure and low temperature in continental margin sediments. Since the discovery of a large number of gas flares at the landward termination of the gas hydrate stability zone off Svalbard, there has been concern that warming bottom waters have started to dissociate large amounts of gas hydrate and that the resulting methane release may possibly accelerate global warming. Here, we can corroborate that hydrates play a role in the observed seepage of gas, but we present evidence that seepage off Svalbard has been ongoing for at least three thousand years and that seasonal fluctuations of 1-2°C in the bottom-water temperature cause periodic gas hydrate formation and dissociation, which focus seepage at the observed sites.
    Keywords: Center for Marine Environmental Sciences; GEOMAR; Helmholtz Centre for Ocean Research Kiel; MARUM
    Type: Dataset
    Format: application/zip, 29 datasets
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  • 3
    Publication Date: 2024-02-02
    Keywords: Age, dated; Age, error; Age model; Calculated; Carbonates; Depth, bottom/max; DEPTH, sediment/rock; Depth, top/min; Description; Error, absolute; Event label; JAGO; Latitude of event; Location; Longitude of event; Maria S. Merian; Mass spectrometer, Finnigan, MAT 253; MC-ICP-MS, isotope dilution; MSM21/4; MSM21/4_579-1; MSM21/4_597-1; non-silicates, total; North Greenland Sea; Sample code/label; Sample mass; Submersible JAGO; Thorium-230/Thorium-232 activity ratio; Thorium-230/Uranium-234 activity ratio; Thorium-232; Uranium-234/Uranium-238 activity ratio; Uranium-234/Uranium-238 activity ratio, error, absolute; Uranium-238; Uranium-238/Thorium-232 activity ratio; X-ray diffractometry (Philips PW1710); δ13C, carbonate; δ18O, carbonate
    Type: Dataset
    Format: text/tab-separated-values, 119 data points
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  • 4
    Publication Date: 2024-02-02
    Keywords: Age, dated; Age, error; Age model; Calculated; Carbonates; Depth, bottom/max; DEPTH, sediment/rock; Depth, top/min; Description; Error, absolute; GC; Gravity corer; Location; Maria S. Merian; Mass spectrometer, Finnigan, MAT 253; MC-ICP-MS, isotope dilution; MSM21/4; MSM21/4_657-1; non-silicates, total; North Greenland Sea; Sample code/label; Sample mass; Thorium-230/Thorium-232 activity ratio; Thorium-230/Uranium-234 activity ratio; Thorium-232; Uranium-234/Uranium-238 activity ratio; Uranium-234/Uranium-238 activity ratio, error, absolute; Uranium-238; Uranium-238/Thorium-232 activity ratio; X-ray diffractometry (Philips PW1710); δ13C, carbonate; δ18O, carbonate
    Type: Dataset
    Format: text/tab-separated-values, 281 data points
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  • 5
    Publication Date: 2019-10-17
    Description: Methane hydrate is an icelike substance that is stable at high pressure and low temperature in continental margin sediments. Since the discovery of a large number of gas flares at the landward termination of the gas hydrate stability zone off Svalbard, there has been concern that warming bottom waters have started to dissociate large amounts of gas hydrate and that the resulting methane release may possibly accelerate global warming. Here, we can corroborate that hydrates play a role in the observed seepage of gas, but we present evidence that seepage off Svalbard has been ongoing for at least three thousand years and that seasonal fluctuations of 1-2°C in the bottom-water temperature cause periodic gas hydrate formation and dissociation, which focus seepage at the observed sites.
    Type: Article , PeerReviewed
    Format: text
    Format: audio
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  • 6
    Publication Date: 2017-09-28
    Description: Microbial aerobic methane oxidation (MOx) is intrinsically coupled to the production of carbon dioxide, favoring carbonate dissolution. Recently, microbial organic polymers were shown to be able to induce carbonate dissolution. To discriminate between different mechanisms causing calcite dissolution, experiments were conducted in the presence of solid calcite with (1) actively growing cells (2) starving cells, and (4) dead cells of the methanotrophic bacterium Methylosinus trichosporium under brackish conditions (salinity 10) near calcite saturation (saturation state (Ω) 1.76 to 2.22). Total alkalinity and the amount of dissolved calcium markedly increased in all experiments containing M. trichosporium cells. After initial system equilibration, similar calcite dissolution rates, ranging between 14.9 (dead cells) and 29.6 μmol l−1 d−1 (actively growing cells), were observed. While concentrations of transparent exopolymer particles declined with time in the presence of actively growing and starving cells, they increased in experiments with dead cells. Scanning electron microscopy images of calcite crystals revealed visible surface corrosion after exposure to live and dead M. trichosporium cells. The results of this study indicate a strong potential for microbial MOx to affect calcite stability negatively, facilitating calcite dissolution. In addition to CO2 production by methanotrophically active cells, we suggest that the release of acidic or Ca2+-chelating organic carbon compounds from dead cells could also enhance calcite dissolution.
    Type: Article , PeerReviewed
    Format: text
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  • 7
    Publication Date: 2019-09-23
    Description: Highlights: • The Giant Gjallar Vent is still active in terms of fluid migration and faulting. • The Base Pleistocene Unconformity acts as a seal to upward fluid migration. • Seal bypass in at least one location leads to a new phase of fluid venting. The Giant Gjallar Vent (GGV), located in the Vøring Basin off mid-Norway, is one of the largest (~ 5 × 3 km) vent systems in the North Atlantic. The vent represents a reactivated former hydrothermal system that formed at about 56 Ma. It is fed by two pipes of 440 m and 480 m diameter that extend from the Lower Eocene section up to the Base Pleistocene Unconformity (BPU). Previous studies based on 3D seismic data differ in their interpretations of the present activity of the GGV, describing the system as buried and as reactivated in the Upper Pliocene. We present a new interpretation of the GGV’s reactivation, using high-resolution 2D seismic and Parasound data. Despite the absence of geochemical and hydroacoustic indications for fluid escape into the water column, the GGV appears to be active because of various seismic anomalies which we interpret to indicate the presence of free gas in the subsurface. The anomalies are confined to the Kai Formation beneath the BPU and the overlying Naust Formation, which are interpreted to act as a seal to upward fluid migration. The seal is breached by focused fluid migration at one location where an up to 100 m wide chimney-like anomaly extends from the BPU up to the seafloor. We propose that further overpressure build-up in response to sediment loading and continued gas ascent beneath the BPU will eventually lead to large-scale seal bypass, starting a new phase of venting at the GGV.
    Type: Article , PeerReviewed
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  • 8
    Publication Date: 2019-10-24
    Description: Sulfate-reducing bacteria are known to mediate dolomite formation under hypersaline conditions, but details of the crystal nucleation process are still poorly constrained. Our laboratory study demonstrates for the first time that Desulfobulbus mediterraneus, a marine sulfate-reducing bacterium, mediates primary precipitation of Mg-rich dolomite under anoxic conditions in media replicating modern seawater chemistry at low temperature (21 °C). Precipitation of crystals was associated with extracellular polymeric substances in a monospecific biofilm, providing templates for nucleation by altering the molar Mg/Ca ratio. After initial nucleation of single nanospherulites (∼50 nm), growth was mediated by aggregation, resulting in spherulites of ∼2–3 μm in diameter. Nucleation led to differences in Mg/Ca ratios and δ44/40Ca values among the organic material (i.e., biofilm including cells and extracellular polymeric substances; 0.87 ± 0.01 [2 SD] and 0.48‰ ± 0.11‰ [2 SE], respectively), the crystals (1.02 ± 0.11 [2 SD] and 〈−0.08‰ ± 0.24‰ [2 SE], respectively), and the liquid bulk medium after mineral precipitation (4.53 ± 0.04 [2 SD] and 1.10‰ ± 0.24‰ [2 SE], respectively). These data indicate a two-step fractionation process involved in the sequestration of Ca from the solution into the crystal lattice of the mineral precipitated. Our results demonstrate the capability of extracellular polymeric substances to overcome kinetic inhibition, fostering the formation of kinetically less favorable Mg-rich dolomite, and they also question the applicability of the Ca isotopic system as a proxy for paleogeochemistry of seawater.
    Type: Article , PeerReviewed , info:eu-repo/semantics/article
    Format: text
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  • 9
    Publication Date: 2019-09-23
    Description: Subduction of the oceanic Cocos plate offshore Costa Rica causes strong advection of methane-charged fluids. Presented here are the first direct measurements of microbial anaerobic oxidation of methane (AOM) and sulfate reduction (SR) rates in sediments from the two mounds, applying radiotracer techniques in combination with numerical modeling. In addition, analysis of carbonate δ18O, δ13C, and 87Sr / 86Sr signatures constrain the origin of the carbonate-precipitating fluid. Average rates of microbial activities showed differences with a factor of 4.8 to 6.3 between Mound 11 [AOM 140.71 (±40.84 SD); SR 117.25 (±82.06 SD) mmol m−2 d−1, respectively] and Mound 12 [AOM 22.37 (±0.85 SD); SR 23.99 (±5.79 SD) mmol m−2 d−1, respectively]. Modeling results yielded flow velocities of 50 cm a−1 at Mound 11 and 8–15 cm a−1 at Mound 12. Analysis of oxygen and carbon isotope variations of authigenic carbonates from the two locations revealed higher values for Mound 11 (δ18O: 4.7 to 5.9‰, δ13C: −21.0 to −29.6‰), compared to Mound 12 (δ18O: 4.1 to 4.5‰, δ13C: −45.7 to −48.9‰). Analysis of carbonates 87Sr / 86Sr indicated temporal changes of deep-source fluid admixture at Mound 12. The present study is in accordance with previous work supporting considerable differences of methane flux between the two Mounds. It also strengthens the hypothesis of a predominantly deep fluid source for Mound 11 versus a rather shallow source of biogenic methane for Mound 12. The results demonstrate that methane-driven microbial activity is a valid ground truthing tool for geophysical measurements of fluid advection and constraining of recent methane fluxes in the study area. The study further shows that the combination of microbial rate measurements, numerical modeling, and authigenic carbonate analysis provide a suitable approach to constrain temporal and spatial variations of methane charged fluid flow at the Pacific Costa Rican margin.
    Type: Article , PeerReviewed
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  • 10
    Publication Date: 2017-06-19
    Description: Two ∼6 m long sediment cores were collected along the ∼300 m isobath on the Alaskan Beaufort Sea continental margin. Both cores showed distinct sulfate-methane transition zones (SMTZ) at 105 and 120 cm below seafloor (cmbsf). Sulfate was not completely depleted below the SMTZ but remained between 30 and 500 μM. Sulfate reduction and anaerobic oxidation of methane (AOM) determined by radiotracer incubations were active throughout the methanogenic zone. Although a mass balance could not explain the source of sulfate below the SMTZ, geochemical profiles and correlation network analyses of biotic and abiotic data suggest a cryptic sulfur cycle involving iron, manganese and barite. Inhibition experiments with molybdate and 2-bromoethanesulfonate (BES) indicated decoupling of sulfate reduction and AOM and competition between sulfate reducers and methanogens for substrates. While correlation network analyses predicted coupling of AOM to iron reduction, the addition of manganese or iron did not stimulate AOM. Since none of the classical archaeal anaerobic methanotrophs (ANME) were abundant, the involvement of unknown or unconventional phylotypes in AOM is conceivable. The resistance of AOM activity to inhibitors implies deviation from conventional enzymatic pathways. This work suggests that the classical redox cascade of electron acceptor utilization based on Gibbs energy yields does not always hold in diffusion-dominated systems, and instead biotic processes may be more strongly coupled to mineralogy.
    Type: Article , PeerReviewed
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