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    Publication Date: 2019-07-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , peerRev
    Format: application/pdf
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  • 3
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    In:  EPIC3GeoDarmstadt2010, Jahrestagung der Deutschen Gesellschaft für Geowissenschaften (DGG) und der Geologischen Vereinigung (GV), Darmstadt.-13. October 2010., 10
    Publication Date: 2019-07-17
    Description: CO2-consumption by chemical weathering of silicates and resulting silicate/carbonate weathering ratios influences long-term climate changes. However, little is known of the spatial extension of highly active weathering regions and their proportion of global CO2-consumption. As those regions may be of significant importance for global climate change, global CO2-consumption is calculated here at high resolution, to adequately represent them. In previous studies global CO2-consumption is estimated using two different approaches: i) a reverse approach based on hydrochemical fluxes from large rivers and ii) a forward approach applying spatially explicit a function for CO2-consumption. The first approach results in an estimate without providing a spatial resolution for highly active regions and the second approach applied six lithological classes while including three sediment classes (shale, sandstone and carbonate rock) based at a 1° or 2° grid resolution. It remained uncertain, if the applied lithological classification schemes represent adequately CO2-consumption from sediments on a global scale. This is due to the large variability of sediment properties, their diagenetic history and the contribution from carbonates apparent in silicate dominated lithological classes. To address these issues, a CO2-consumption model, trained at high-resolution data, is applied here to a global vector based lithological map with 15 lithological classes. The calibration data were obtained from areas representing a wide range of weathering rates. Resulting global CO2-consumption by chemical weathering is similar to earlier estimates (237 Mt C a− 1) but the proportion of silicate weathering is 63%, and thus larger than previous estimates (49 to 60%). The application of the enhanced lithological classification scheme reveals that it is important to distinguish among the various types of sedimentary rocks and their diagenetic history to evaluate the spatial distribution of rock weathering. Results highlight the role of hotspots (〉 10 times global average weathering rates) and hyperactive areas (5 to 10 times global average rates). Only 9% of the global exorheic area is responsible for about 50% of CO2-consumption by chemical weathering (or if hotspots and hyperactive areas are considered: 3.4% of exorheic surface area corresponds to 28% of global CO2-consumption). The contribution of endorheic areas to the global CO2-consumption is with 3.7 Mt C a− 1 only minor. A significant impact on the global CO2-consumption rate can be expected if identified highly active areas are affected by changes in the overall spatial patterns of the hydrological cycle due to ongoing global climate change. Specifically if comparing the Last Glacial Maximum with present conditions it is probable that also the global carbon cycle has been affected by those changes. It is expected that results will contribute to improve global carbon and global circulation models.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Conference , notRev
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  • 4
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    Unknown
    In:  EPIC3Geophysical Research Abstracts, 12, EGU2010-7141-1, EGU General Assembly, 2010 p.
    Publication Date: 2019-07-17
    Description: CO2-consumption by chemical weathering of silicates and resulting silicate/carbonate weathering ratios influences the terrestrial lateral inorganic carbon flux to the ocean and long-term climate changes. However, little is known of the spatial extension of highly active weathering regions and their proportion of global CO2-consumption. As those regions may be of significant importance for global climate change, global CO2-consumption is calculated here at high resolution, to adequately represent them. In previous studies global CO2-consumption is estimated using two different approaches: i) a reverse approach based on hydrochemical fluxes from large rivers and ii) a forward approach applying spatially explicit a function for CO2-consumption. The first approach results in an estimate without providing a spatial resolution for highly active regions and the second approach applied six lithological classes while including three sediment classes (shale, sandstone and carbonate rock) based at a 1° or 2° grid resolution. It remained uncertain, if the applied lithological classification schemes represent adequately CO2-consumption from sediments on a global scale (as well as liberation of other elements like phosphorus or silicon by chemical weatheirng). This is due to the large variability of sediment properties, their diagenetic history and the contribution from carbonates apparent in silicate dominated lithological classes. To address these issues, a CO2-consumption model, trained at high-resolution data, is applied here to a global vector based lithological map with 15 lithological classes. The calibration data were obtained from areas representing a wide range of weathering rates. Resulting global CO2-consumption by chemical weathering is similar to earlier estimates (237 MtC/a) but the proportion of silicate weathering is 63%, and thus larger than previous estimates (49 to 60%). The application of the enhanced lithological classification scheme reveals that it is important to distinguish among the various types of sedimentary rocks and their diagenetic history to evaluate the spatial distribution of rock weathering and thus lateral inorganic carbon fluxes. Results highlight the role of hotspots (〉10 times global average weathering rates) and hyperactive areas (5 to 10 times global average rates). Only 9% of the global exorheic area is responsible for about 50% of CO2- consumption by chemical weathering (or if hotspots and hyperactive areas are considered: 3.4% of exorheic surface area corresponds to 28% of global CO2-consumption). The contribution of endorheic areas to the global CO2-consumption is with 3.7 MtC/a only minor. A significant impact on the global CO2-consumption rate can be expected if identified highly active areas are affected by changes in the overall spatial patterns of the hydrological cycle due to ongoing global climate change. Specifically if comparing the Last Glacial Maximum with present conditions it is probable that also the global carbon cycle has been affected by those changes. It is expected that results will contribute to improve global carbon and global circulation models. In addition, recognizing chemical weathering rates and geochemical composition of certain lithological classes may be of value for studies focusing on biological aspects of the carbon cycles (e.g. studies needing information on the abundance of phosphorus or silica in the soil or aquatic system).
    Repository Name: EPIC Alfred Wegener Institut
    Type: Conference , notRev
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  • 5
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 87 (2000), S. 5466-5468 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The evolving magnetism and electronic structure at the Ni/Co interface have been studied using x-ray absorption spectroscopy (XAS) and x-ray photoemission spectroscopy (XPS) with circularly polarized x rays. Deposition of ultrathin Ni films on thin films of Co grown on Cu(001) results in an intensity enhancement across the Co L2.3 absorption edge. By comparison, the intensity of the Ni L2.3 edge decreases as a function of Ni film thickness. The relative changes in the Ni and Co XAS intensities are interpreted as an electronic charge transfer from the Co to the Ni. Distinct changes in the Co 2p XAS and XPS line shapes after addition of the Ni overlayer imply a modification of the Co 3d electron correlation due to the charge transfer. The change in the electronic structure is related to the interface magnetism using magnetic circular dichroism sum rule analysis. © 2000 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 87 (2000), S. 5469-5471 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Depending on the growth conditions, FePd thin films can display a perpendicular magnetic anisotropy associated with chemical order. In competition with the shape anisotropy, this can lead to striped magnetic domains, with moments perpendicular to the film plane. Under these circumstances, magnetic flux closure should occur. The striped domains were studied with soft x-ray resonant magnetic scattering using circularly polarized light to demonstrate the presence of closure domains. Magnetic depth profiling was performed both at the Fe and Pd L3 edge, by measuring the magnetic diffraction peak intensities versus angle of incidence θ. © 2000 American Institute of Physics.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Naturwissenschaften 64 (1977), S. 443-444 
    ISSN: 1432-1904
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Chester : International Union of Crystallography (IUCr)
    Journal of synchrotron radiation 7 (2000), S. 178-181 
    ISSN: 1600-5775
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: The method of circular dichroism in X-ray resonant magnetic scattering is presented which allows a straightforward determination of the magnetization profile of magnetic patterns in ultrathin films. Application to single crystalline FePd layers shows unambiguously the presence of magnetic flux closure domains whose thickness can constitute a significant fraction (∼25%) of the total film.
    Type of Medium: Electronic Resource
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  • 9
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