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  • 1980-1984  (11)
  • 1970-1974  (3)
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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of chemical & engineering data 16 (1971), S. 398-400 
    ISSN: 1520-5134
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Sill intrusions into highly porous sediments in the Guaymas Basin, Gulf of California, lead to low-grade metamorphism, thermal alteration and migration of organic compounds, marked changes in interstitial water chemistry, and large-scale expulsion of heated pore fluids. The latter process creates ...
    Type of Medium: Electronic Resource
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  • 3
    Publication Date: 2022-06-17
    Description: Changes in the dissolved oxygen content, the alkalinity, and the pH in sea water near the ocean floor are interpreted in terms of chemical and biochemical processes at the sediment water interface. A simple model provides a plausible explanation of the observed phenomena. Special emphasis is given to the importance of borate corrections in the calculation of the solution effects of calcium carbonate.
    Type: Article , PeerReviewed
    Format: text
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  • 4
    Publication Date: 2022-06-22
    Description: Hydrographie data (salinity, temperature, oxygen, silicate, and phosphate) obtained on 5 stations ("Meteor" cruise 23, leg C, 8 to 26 June 1971) on a section from Lisbon, Portugal, to 44° N, 43° W (Newfoundland Basin) by both water sampling and in situ observation by the "Bathysonde" (STD), are summarized. A strong core of Mediterranean water was found at the eastern boundary of the section (38.5° N, 11.5° W). At this station, the core is accompanied by low nutrient concentrations and brings about an extended oxygen minimum (ca. 500 to 1400 m depth). The core quickly weakens towards the west and is, at the Mid-Atlantic Ridge, only apparent in the Bathysonde data. Two salinity maxima are observed within the core of Mediterranean water, the center of which speads along the isopycnal σt = 27.7. Dissolved oxygen shows a rapid concentration increase with depth below the Mediterranean water core; concentration variations with depth below the range of this increase are only small. The mean deep-water oxygen concentration increases from 5.5 ml/kg (below 2500 m) to 6.20 ml/kg (below 1500 m) in an east-west direction on the section. The upper boundary of the deep-water oxygen concentration range thereby rises from 2000 to 1300 m; this boundary marks the upper boundary of the Arctic Intermediate water. Core depths of Arctic Intermediate and of Iceland-Scotland overflow water, are derived from the potential-temperature/salinity diagrams obtained in the western basin, and are extended to the other stations by assuming lateral spreading to occur along isopycnal surfaces. The core depths for the Intermediate water obtained in this manner, are supported also by the potential-temperature to silicate relations. The bottom water of the westernmost station of the section, at 44° N, 43° W, is of Denmark Strait origin, and it produces a distinct reversal in the vertical trends of salinity, silicate, phosphate, and oxygen, at 4300 m depth. The concentration of the nuclear-weapon produced nuclide tritium increases within the Denmark Strait water core towards the bottom. Further tritium concentration peaks appear in the intermediate and deep water at this station. At the next Station east on the section at 43° N 34 ° W, tritium concentrations are essetially zero below 2000 m depth, and are distinctly smaller than on the westernmost station, between 600 m and 2000 m depth. This "Meteor" section was track F of the Atlantic network of the international Geochemical Ocean Sections Program (GEOSECS).
    Type: Article , PeerReviewed
    Format: text
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  • 5
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    Society of Sedimentary Geology
    In:  Journal of Sedimentary Petrology, 52 (1). pp. 71-82.
    Publication Date: 2015-09-15
    Description: Laboratory determinations of the distribution coefficient of strontium in calcite (k Sr ) have confirmed the earlier results of Katz et al. (1972). In addition, we observed that at higher concentrations of strontium, values of k Sr were somewhat lowered. Chemical analyses of several deep-sea carbonate sediment sections and their associated porewaters (DSDP Sites 288, 289, 315, 317, and 357) as well as previously published data of other workers (DSDP Sites 116 and 305) have been used to demonstrate that these k Sr values are appropriate for use in diagenetic studies. We have successfully modeled the distribution of strontium in the pore waters and sediments. As a result, we conclude that recrystallization of these carbonates (and many other limestones as well) is essentially isochemical, the cement being derived from within the formation. Advective fluid flow through the rock is unnecessary to explain its lithification. Recrystallization of the bulk of the calcite in deep-sea sections is largely complete within the upper few hundred meters, but cementation is generally a later process. These results have important implications for the study of oxygen isotopic compositions of foraminifers and coccoliths in many sediments older than about 20 m.y. B.P. From correlations between changes in Sr/Ca and Mg/Ca ratios of recrystallized carbonates of DSDP Site 305 a distribution coefficient of magnesium in calcite sediments of 8.1 x 10- 4 ( nearly equal 5 degrees C) has been estimated. This value is many times smaller than previously published values.
    Type: Article , PeerReviewed
    Format: text
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  • 6
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    PANGAEA
    In:  Supplement to: Elderfield, Henry; Gieskes, Joris M; Baker, Paul A; Oldfield, R K; Hawkesworth, Chris J; Miller, R (1982): 87Sr/88Sr and 18O/16O ratios, interstitial water chemistry and diagenesis in deep-sea carbonate sediments of the Ontong Java Plateau. Geochimica et Cosmochimica Acta, 46(11), 2259-2268, https://doi.org/10.1016/0016-7037(82)90199-5
    Publication Date: 2024-02-10
    Description: Interstitial waters and sediments from DSDP sites 288 and 289 contain information on the chemistry and diagenesis of carbonate in deep-sea sediments and on the role of volcanic matter alteration processes. Sr/Ca ratios are species dependent in unaltered foraminifera from site 289 and atom ratios (0.0012-0.0016) exceed those predicted by distribution coefficent data (~0.0004). During diagenesis Sr/Ca ratios of carbonates decrease and reach the theoretical distribution at a depth which is identical to the depth of Sr isotopic equilibration, where 87Sr/86Sr ratios of interstitial waters and carbonates converge. Mg/Ca ratios in the carbonates do not increase with depth as found in some other DSDP sites, possibly because of diagenetic re-equilibration with interstitial waters showing decreasing Mg(2+)/Ca(2+) ratios with depth due to Ca input and Mg removal by alteration of volcanic matter. Interstitial 18O/16O ratios increase with depth at site 289 to d18O = 0.67‰ (SMOW), reflecting carbonate recrystallization at elevated temperatures (〉/= 20°C), the first recorded evidence of this effect in interstitial waters. Interstitial Sr2+ concentrations reach high levels, up to 1 mM, chiefly because of carbonate recrystallization. However, 87Sr/86Sr ratios decrease from 0.7092 to less than 0.7078, lower than for contemporaneous sea water, showing that there is a volcanic input of strontium at depth. This volcanic component is recorded in the Sr isotopic composition of recrystallized calcites. Isotopic compositions of the unrecrystallized calcites suggests that the rate of increase of the 87Sr/86Sr ratio of sea water with time has been faster since 3 my ago than in the preceding 13 my.
    Keywords: 30-288; 30-288A; 30-289; Deep Sea Drilling Project; DRILL; Drilling/drill rig; DSDP; Glomar Challenger; Leg30; South Pacific; South Pacific/PLATEAU
    Type: Dataset
    Format: application/zip, 6 datasets
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  • 7
    Publication Date: 2024-02-10
    Keywords: 30-289; Deep Sea Drilling Project; DEPTH, sediment/rock; DRILL; Drilling/drill rig; DSDP; DSDP/ODP/IODP sample designation; Glomar Challenger; Leg30; Sample code/label; South Pacific/PLATEAU; δ13C; δ18O
    Type: Dataset
    Format: text/tab-separated-values, 49 data points
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  • 8
    Publication Date: 2024-02-10
    Keywords: 30-289; Atomic absorption spectrometry (AAS); Calcium carbonate; Calculated; Deep Sea Drilling Project; DEPTH, sediment/rock; DRILL; Drilling/drill rig; DSDP; DSDP/ODP/IODP sample designation; EGTA titration (Tsunogai et al., 1968); Glomar Challenger; Leg30; Magnesium; Magnesium/Calcium ratio; Sample code/label; South Pacific/PLATEAU; Strontium; Strontium/Calcium ratio
    Type: Dataset
    Format: text/tab-separated-values, 132 data points
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  • 9
    Publication Date: 2024-02-10
    Keywords: 30-288; 30-288A; Alkalinity, total; Atomic absorption spectrometry (AAS); Atomic emission spectroscopy (AES); Calcium; Deep Sea Drilling Project; DEPTH, sediment/rock; DRILL; Drilling/drill rig; DSDP; DSDP/ODP/IODP sample designation; Event label; Glomar Challenger; Leg30; Magnesium; pH; Potassium; Punch-in electrode; Refractometer, Goldberg; Salinity; Sample code/label; Seawater analysis (Strickland & Parsons, 1968); Silicon; South Pacific; Strontium; Sulfate; Titration; Titration complexometric; Titration potentiometric
    Type: Dataset
    Format: text/tab-separated-values, 107 data points
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  • 10
    Publication Date: 2024-02-10
    Keywords: 30-288; 30-288A; Atomic absorption spectrometry (AAS); Calcium carbonate; Calculated; Deep Sea Drilling Project; DEPTH, sediment/rock; DRILL; Drilling/drill rig; DSDP; DSDP/ODP/IODP sample designation; EGTA titration (Tsunogai et al., 1968); Event label; Glomar Challenger; Leg30; Magnesium; Magnesium/Calcium ratio; Sample code/label; South Pacific; Strontium; Strontium/Calcium ratio
    Type: Dataset
    Format: text/tab-separated-values, 90 data points
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