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  • 2010-2014  (4)
  • 1995-1999  (8)
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  • 1
    Keywords: Datensammlung
    Description / Table of Contents: 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 (delta 18Of) 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 delta18Of 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.
    Type of Medium: Online Resource
    Pages: 3 Datasets , Format: application/zip
    Language: English
    Note: This dataset is supplement to doi:10.1016/S0012-821X(98)00097-1
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  • 2
    ISSN: 1433-4909
    Keywords: Key words Hyperthermophilic ; Crenarchaeota ; Hydrogen and sulfur dependence ; Hydrothermal ; Stetteria hydrogenophila
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A new hyperthermophilic, strictly anaerobic crenarchaeote, Stetteria hydrogenophila DSM11227 representing a new genus within the family of Desulfurococcaceae, was isolated from the sediment of a marine hydrothermal system at Paleohori Bay in Milos, Greece. Cells are gram-negative irregular and disc-shaped cocci, 0.5–1.5 μm in diameter, which are flagellate and can form cytoplasmatic protrusions up to 2 μm in length. The strain grew optimally at 95°C at pH 6.0 and at a NaCl concentration of 3%. The organism grew mixotrophically on peptide substrates. It required elemental sulfur as an external electron acceptor, and in addition, its growth was completely dependent on the presence of molecular hydrogen. Sulfur could be replaced by thiosulfate. H2S, CO2, acetate, and ethanol were identified as products of metabolism. The G + C content of DNA was 65 mol%. Analysis of its phylogenetic position by sequence analysis of 16S rRNA placed this organism in the family of Desulfurococcaceae. The dependence of this organism on both hydrogen and sulfur during growth on peptide substrates distinguishes Stetteria from all previously described species of Crenarchaeota.
    Type of Medium: Electronic Resource
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  • 3
    Publication Date: 2019-09-23
    Description: Magnesium calcites were synthesized from aqueous solutions supersaturated with respect to calcite at 25, 40, 60, and 80 °C in gas tight batch reactors for up to 35 days. Any amorphous material still present in the precipitates was removed using a partial dissolution treatment. Resulting purified Mg-calcite had Mg contents ranging from 6 to 32 mol% MgCO3. An isotopic steady-state was attained between the fluid and the precipitated solids within two weeks at 25 °C. δ18O values derived from the experiments at steady-state, depend on both temperature and the Mg content of the calcite in accord with: 1000lnαMg-calcite–H2O=18,030/T−32.42+(6×108/T3–5.47×106/T2+16,780/T−17.21)×CMg where αMg-calcite–H2O represents the calcite–water oxygen isotope fractionation factor, T refers to the temperature in °K and CMg denotes the mole percent of MgCO3 in the calcite. These results indicate that the addition of 5 mol% MgCO3 into the calcite increases 1000lnαMg-calcite–H2O by 0.88 as compared to that of pure calcite at 25 °C. This difference could lead to a 4.2 °C decrease in estimated formation temperature estimates. These results demonstrate that the accurate interpretation of oxygen isotope fractionation in magnesium calcites requires explicit provision for the effect of magnesium on oxygen isotope fractionation factors. Highlights ► The effect of Mg on calcite–aqueous fluid oxygen isotope fractionation was investigated. ► Mg incorporation is increasing the calcite–aqueous fluid oxygen isotope fractionation. ► This effect is reduced at higher temperatures. ► Obtained results are important for paleo-temperature estimation. Gadget timed out while loading
    Type: Article , PeerReviewed
    Format: text
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  • 4
    Publication Date: 2019-09-23
    Description: The surface sediments of two mud mounds (‘‘Mound 11’’ and ‘‘Mound 12’’) offshore southwest Costa Rica contain abundant authigenic carbonate concretions dominated by high-Mg calcite (14–20 mol-% MgCO3). Pore fluid geochemical profiles (sulfate, sulfide, methane, alkalinity, Ca and Mg) indicate recent carbonate precipitation within the zone of anaerobic oxidation of methane (AOM) at variable depths. The current location of the authigenic carbonate concretions is, however, not related to the present location of the AOM zone, suggesting mineral precipitation under past geochemical conditions as well as changes in the flow rates of upward migrating fluids. Stable oxygen and carbon isotope analysis of authigenic carbonate concretions yielded d18Ocarbonate values ranging between 34.0 and 37.7 % Vienna standard mean ocean water (VSMOW) and d13Ccarbonate values from -52.2 to -14.2 % Vienna Pee Dee belemnite (VPDB). Assuming that no temperature changes occurred during mineral formation, the authigenic carbonate concretions have been formed at in situ temperature of 4–5 °C. The d18Ocarbonate values suggest mineral formation from seawater-derived pore fluid (d18Oporefluid = 0 % VSMOW) for Mound 12 carbonate concretions but also the presence of an emanating diagenetic fluid (d18Oporefluid &5 %) in Mound 11. A positive correlation between d13Ccarbonate and d18Ocarbonate is observed, indicating the admixing of two different sources of dissolved carbon and oxygen in the sediments of the two mounds. The carbon of these sources are (1) marine bicarbonate (d13Cporefluid &0 %) and (2) bicarbonate which formed during the AOM (d13Cporefluid &-70 %). Furthermore, the d18Oporefluid composition, with values up to ?4.7 % Vienna standard mean ocean water (VSMOW), is interpreted to be affected by the presence of emanating, freshened and boronenriched fluids. Earlier, it has been shown that the origin of 18O-enriched fluids are deep diagenetic processes as it was indicated by the presence of methane with thermogenic signature (d13CCH4 = -38 %). A combination of present geochemical data with geophysical observations indicates that Mounds 11 and 12 represent a single fluid system interconnected by deep-seated fault(s).
    Type: Article , PeerReviewed
    Format: text
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  • 5
    Publication Date: 2017-12-07
    Description: Parasound profiles across the Shaban Deep in the Red Sea indicate turbiditic transport of surface sediments from the topographic hight (basalt ridge) into the interior of the deep. This is supported by petrographical and (isotope-) geochemical evidence in the East Basin of the Shaban Deep where the presence of variable mixtures of authochtonous and allochthonous sediment compounds had been found. The uppermost 170 cm of both sediment cores 17008-1 and 17009-3 reveal “normal” stable oxygen isotope values for the planktonic foraminifera G. ruber near -1 ‰ which is indicative for carbonate formation in Red Sea surface water around 27°C. However, below 182 cm in core 17008-1 highly variable δ 18O values for G. ruber between 0.26 and -10.68 ‰ occur which are not the result of temperature-controlled oxygen isotope fractionation between foraminiferal carbonate and Red Sea surface water. The lowest δ18O values of -10.68 ‰ measured for highly-altered foraminifera shells suggests carbonate precipitation higher than 90°C. Organic petrographical observations show a great diversity of marine-derived macerals and terrigenous organic particles. Based on petrographical investigations sediment core 17008-1 can be subdivided in intervals predominantly of authochtonous character (i.e. 1, 3, 5 corresponding to core depths 0-170 cm, 370-415 cm, 69-136 cm), and allochthonous/thermally altered character (e.g. 2, 4 corresponding to core depths 189-353 cm, 515-671 cm). Allochthonous/thermally altered material displays a wide to an extremely wide range of maturities (0.38-1.42 % Rr) and also natural coke particles were found. Similarily, the organic geochemical and pyrolysis data indicate the predominance of well-preserved, immature algal and bacterial remains with a minor contribution of land plant material. Sediments below 170 cm (core 17008-1) contain contributions of re-sedimented pre-heated material most likely from the area of the basaltic ridge. This is documented by individual coke particles reduced hydrogen indices and elevated Tmax values up to 440°C. An “oil-type” contribution (evidenced by mature biomarkers, hopene/hopane ratios, elevated background fluorescence, n-alkane distribution) is also present in the sediments which most likely originated at greater depth and impregnated the surface sediments. The heat source responsible for recrystallisation of foraminiferal carbonate and maturation of organic particles in Shaban Deep sediments most likely is attributed to modern basalt extrusions which now separate the Shaban Deep subbasins.
    Type: Article , PeerReviewed
    Format: text
    Format: text
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  • 6
  • 7
    Publication Date: 2024-01-09
    Keywords: 110-672A; DEPTH, sediment/rock; DRILL; Drilling/drill rig; DSDP/ODP/IODP sample designation; Fractionation factor; Joides Resolution; Leg110; Mass spectrometer Finnigan MAT 251; Ocean Drilling Program; ODP; Sample code/label; South Atlantic Ocean; Temperature, calculated; Temperature, in rock/sediment; Temperature, standard deviation; δ18O
    Type: Dataset
    Format: text/tab-separated-values, 54 data points
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  • 8
    Publication Date: 2024-01-09
    Keywords: 122-762B; 122-762C; DEPTH, sediment/rock; DRILL; Drilling/drill rig; DSDP/ODP/IODP sample designation; Event label; Fractionation factor; Joides Resolution; Leg122; Mass spectrometer Finnigan MAT 251; Ocean Drilling Program; ODP; Sample code/label; South Indian Ridge, South Indian Ocean; Temperature, calculated; Temperature, in rock/sediment; Temperature, standard deviation; δ18O
    Type: Dataset
    Format: text/tab-separated-values, 93 data points
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  • 9
    Publication Date: 2024-01-09
    Keywords: 127-797B; DEPTH, sediment/rock; DRILL; Drilling/drill rig; DSDP/ODP/IODP sample designation; Fractionation factor; Japan Sea; Joides Resolution; Leg127; Mass spectrometer Finnigan MAT 251; Ocean Drilling Program; ODP; Sample code/label; Temperature, calculated; Temperature, in rock/sediment; Temperature, standard deviation; δ18O
    Type: Dataset
    Format: text/tab-separated-values, 36 data points
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  • 10
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    PANGAEA
    In:  Supplement to: Nähr, Thomas H; Botz, Reiner; Bohrmann, Gerhard; Schmidt, Mark (1998): Oxygen isotopic composition of low-temperature authigenic clinoptilolite. Earth and Planetary Science Letters, 160(3-4), 369-381, https://doi.org/10.1016/S0012-821X(98)00097-1
    Publication Date: 2024-01-09
    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 (delta 18Of) that extend from +18.7 per mil to +32.8 per mil (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 25ºC to 40ºC. The resulting fractionation factors of 1.032 at 25ºC and 1.027 at 40ºC 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 17ºC to 29ºC in Barbados Ridge sediments and at 33ºC to 62ºC 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 delta18Of values with depth indicate that clinoptilolites which are now in the deeper parts of the zeolite-bearing intervals had either formed at lower temperatures (17-20ºC) or under closed system conditions.
    Keywords: 110-672A; 122-762B; 122-762C; 127-797B; DRILL; Drilling/drill rig; Japan Sea; Joides Resolution; Leg110; Leg122; Leg127; Ocean Drilling Program; ODP; South Atlantic Ocean; South Indian Ridge, South Indian Ocean
    Type: Dataset
    Format: application/zip, 3 datasets
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