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  • 1
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    PANGAEA
    In:  Supplement to: Mackensen, Andreas; Hubberten, Hans-Wolfgang; Scheele, Norbert; Schlitzer, Reiner (1996): Decoupling of d13CSUMCO2 and phosphate in recent Weddell Sea deep and bottom water: implications for glacial Southern Ocean paleoceanography. Paleoceanography, 11(2), 203-215, https://doi.org/10.1029/95PA03840
    Publication Date: 2023-06-27
    Description: On a section between 72°S and 42°S and a transect between 60°E and 10°E through the Weddell Sea and the southernmost eastern Atlantic Ocean, the water column was sampled on 72 stations, and the stable carbon isotopic composition of total dissolved inorganic carbon (delta13C(SumCO2)) as well as the stable oxygen isotopic composition of seawater (delta18O) was determined. These data were compared with potential temperature, salinity, dissolved oxygen and phosphate data from the same stations. The observed delta13C(SumCO2)/PO4[3-] relationship in the deep Weddell Sea strongly differs from the global Redfield-driven deep water relationship. We attribute this to enhanced thermodynamic fractionation at sites of bottom water formation that decouples the nutrient signal from the delta13C(SumCO2) signal not only in surface and intermediate water masses but also in deep and bottom water. Different, water-mass specific thermodynamic imprints due to different modes of bottom water formation are assumed to cause the observed deviation from the global delta13C(SumCO2)/PO4[3-] relationship in the deep Weddell Sea. The influence of increased photosynthetic fractionation, i.e., a more negative than low-latitude isotopic organic carbon composition, is shown to be minor. As a result, Recent Weddell Sea deep and bottom water delta13C(SumCO2) is by 0.4-0.5 per mil higher than expected if solely biologic fractionation would occur. A discussion of simple hypotheses of Weddell Sea deep and bottom water formation during glacial times reveals that regardless of what scenario is considered, the thermodynamic imprint on Southern Ocean deep water would increase. This makes it difficult to explain low glacial delta13C values observed in benthic foraminifera from the subpolar Southern Ocean as being calcified in Antarctic source bottom water and thus is in support of hypotheses looking for additional sites of deep water formation.
    Keywords: Agulhas Basin; ANT-VIII/2; ANT-VIII/3; Atlantic Ridge; AWI_Paleo; Calculated after Broecker & Maier-Reimer 1992; CFA; Continuous Flow Analysis; CTD, Neil Brown, Mark III B; CTD/Rosette; CTD-RO; Date/Time of event; DEPTH, water; Elevation of event; Event label; Indian-Antarctic Ridge; Latitude of event; Longitude of event; Mass spectrometer Finnigan Delta-S; Mass spectrometer Finnigan MAT 252; Meteor Rise; MUC; MULT; MultiCorer; Multiple investigations; Oxygen; Oxygen, Winkler (Culberson, 1991, WOCE Report 68/91); Paleoenvironmental Reconstructions from Marine Sediments @ AWI; Phosphate; Polarstern; Pressure, water; PS16; PS16/119; PS16/124; PS16/129; PS16/134; PS16/137; PS16/140; PS16/143; PS16/145; PS16/146; PS16/147; PS16/149; PS16/150; PS16/151; PS16/152; PS16/153; PS16/154; PS16/155; PS16/156; PS16/157; PS16/159; PS16/162; PS16/164; PS16/166; PS16/167; PS16/169; PS16/171; PS16/172; PS16/174; PS16/176; PS16/177; PS16/179; PS16/180; PS16/182; PS16/183; PS16/184; PS16/185; PS16/186; PS16/187; PS16/188; PS16/189; PS16/192; PS16/193; PS16/194; PS16/195; PS16/197; PS16/198; PS16/199; PS16/200; PS16/201; PS16/202; PS16/203; PS16/204; PS16/205; PS16/207; PS16/208; PS16/209; PS16/210; PS16/211; PS16/212; PS16/213; PS16/217; PS16/219; PS16/221; PS16/262; PS16/267; PS16/281; PS16/294; PS16/297; PS16/311; PS16/316; PS16/321; PS16/323; PS16 06AQANTVIII_2; PS1750-7; PS1751-1; PS1755-2; PS1759-5; PS1760-1; PS1768-4; PS1771-4; PS1772-1; PS1773-3; Salinity; SFB261; Shona Ridge; South Atlantic in Late Quaternary: Reconstruction of Budget and Currents; Temperature, water, potential; Van Heesen Ridge; Water sample; Weddell Sea; WS; Δδ13C; δ13C, dissolved inorganic carbon; δ18O, water
    Type: Dataset
    Format: text/tab-separated-values, 7920 data points
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 112 (1992), S. 35-45 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract The partitioning of stable carbon isotopes between calcite, graphite and CO2 was experimentally determined at temperatures from 500 to 1200 °C and 1 to 15 kbar pressure. Attainment of carbon isotope equilibrium in CO2-calcite runs was proven by achieving the same fractionation from isotopically opposite directions. The resultant CO2-calcite fractionation curve for carbon differs from Bottinga's calculation by 1.2‰ and confirms recent experiments of Chacko et al. and Mattey et al. In CO2-graphite experiments equilibrium fractions were extrapolated by applying the partial-exchange technique of Northrop and Clayton and by optimizing the contribution of surface reaction in graphite. CO2-graphite fractionations at temperatures up to 800 °C are in fair agreement with Bottinga's calculation, but yield a surprisingly high fractionation of ≈5‰ at upper mantle temperatures. The combination of CO2-calcite (carbon) and CO2-graphite fractionation results in a new experimentally determined calcite-grapite fractionation curve, expressed by the equation: $$\begin{gathered} 10^3 {\text{ ln }}\alpha _{{\text{cc - gr}}} = 7.99 \times 10^6 /T^2 - 9.58 \times 10^3 / + 5.76 \hfill \\ {\text{ (873 - 1473 Kelvin)}} \hfill \\ \end{gathered} $$ Applying the experimentally determined fractionation curve on graphite-bearing metacarbonates yields metamorphic temperatures distinctly higher than those obtained by Valley and O'Neil.
    Type of Medium: Electronic Resource
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  • 3
  • 4
    Publication Date: 1992-10-01
    Print ISSN: 0010-7999
    Electronic ISSN: 1432-0967
    Topics: Geosciences
    Published by Springer
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  • 5
    Publication Date: 2017-05-22
    Description: Ikaite crystals (CaCO3×6H2O) have been found at 232- to 238-cm sediment depth in R/V Polarstern core PS2460-4 from the Laptev Sea continental margin in a water depth of 204 m. δ13C values of this phase average −36.3±0.4‰ PDB (N=2), which is significantly outside the range of normal marine carbonates. The CO2 involved in the precipitation of the ikaite is most probably derived from methane, which has extremely depleted 13C isotope values. Two possible sources of methane in these sediments are: (1) methanogenesis (decomposition of organic matter under anaerobic conditions); and (2) gas hydrates, which are known to occur in the Siberian shelf regions.
    Type: Article , PeerReviewed
    Format: text
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