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  • 1
    Series available for loan
    Series available for loan
    Offenbach : Selbstverl. d. Dt. Wetterdienstes
    Associated volumes
    Call number: MOP 36920/1 / DG
    In: Leitfäden für die Ausbildung im Deutschen Wetterdienst
    Type of Medium: Series available for loan
    Pages: 60 S. : graph. Darst., Kt. + 3 Beil.
    Series Statement: Leitfäden für die Ausbildung im Deutschen Wetterdienst 1
    Location: MOP - must be ordered
    Branch Library: GFZ Library
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  • 2
    Monograph available for loan
    Monograph available for loan
    Offenbach, M : Dt. Wetterdienst
    Associated volumes
    Call number: MOP Per 60(24)
    In: Mitteilungen des Deutschen Wetterdienstes
    Type of Medium: Monograph available for loan
    Pages: 24 S. , graph. Darst.
    Series Statement: Mitteilungen des Deutschen Wetterdienstes 24
    Location: MOP - must be ordered
    Branch Library: GFZ Library
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  • 3
    Monograph available for loan
    Monograph available for loan
    Bad Kissingen : Dt. Wetterdienst in d. US-Zone
    Associated volumes
    Call number: MOP Per 18(33)
    In: Berichte des Deutschen Wetterdienstes in der US-Zone
    Type of Medium: Monograph available for loan
    Pages: 39 S.
    Series Statement: Berichte des Deutschen Wetterdienstes in der US-Zone 33
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  • 4
    Monograph available for loan
    Monograph available for loan
    Offenbach a.M. : Dt. Wetterdienstes
    Associated volumes
    Call number: MOP Per 18(113)
    In: Berichte des Deutschen Wetterdienstes
    Type of Medium: Monograph available for loan
    Pages: 14, 56 S. : graph. Darst.
    Edition: 2., neu bearb. u. erg. Aufl.
    Series Statement: Berichte des Deutschen Wetterdienstes 113 = Bd. 15
    Location: MOP - must be ordered
    Branch Library: GFZ Library
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  • 5
    Monograph available for loan
    Monograph available for loan
    Offenbach a.M. : Dt. Wetterdienstes
    Associated volumes
    Call number: MOP Per 18(113)
    In: Berichte des Deutschen Wetterdienstes
    Type of Medium: Monograph available for loan
    Pages: 14, 54 S. : graph. Darst.
    Edition: 3., verb. u. erg. Aufl.
    Series Statement: Berichte des Deutschen Wetterdienstes 113 = Bd. 15
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  • 6
    Publication Date: 2022-05-25
    Description: Author Posting. © Springer, 2008. This is the author's version of the work. It is posted here by permission of Springer for personal use, not for redistribution. The definitive version was published in Contributions to Mineralogy and Petrology 156 (2008): 87-102, doi:10.1007/s00410-007-0275-8.
    Description: The grain-scale processes of peridotite melting were examined at 1340°C and 1.5 GPa using reaction couples formed by juxtaposing pre-synthesized clinopyroxenite against pre-synthesized orthopyroxenite or harzburgite in graphite and platinum-lined molybdenum capsules. Reaction between the clinopyroxene and orthopyroxene-rich aggregates produces a melt-enriched, orthopyroxene-free, olivine + clinopyroxene reactive boundary layer. Major and trace element abundance in clinopyroxene vary systematically across the reactive boundary layer with compositional trends similar to the published clinopyroxene core-to-rim compositional variations in the bulk lherzolite partial melting studies conducted at similar P– T conditions. The growth of the reactive boundary layer takes place at the expense of the orthopyroxenite or harzburgite and is consistent with grain-scale processes that involve dissolution, precipitation, reprecipitation, and diffusive exchange between the interstitial melt and surrounding crystals. An important consequence of dissolution–reprecipitation during crystal melt interaction is the dramatic decrease in diffusive reequilibration time between coexisting minerals and melt. This effect is especially important for high charged, slow diffusing cations during peridotite melting and melt-rock reaction. Apparent clinopyroxenemelt partition coefficients for REE, Sr, Y, Ti, and Zr, measured from reprecipitated clinopyroxene and coexisting melt in the reactive boundary layer, approach their equilibrium values reported in the literature. Disequilibrium melting models based on volume diffusion in solid limited mechanism are likely to significantly underestimate the rates at which major and trace elements in residual minerals reequilibrate with their surrounding melt.
    Description: This work was supported by NSF grants EAR-0208141 and EAR-0510606 to Yan Liang.
    Repository Name: Woods Hole Open Access Server
    Type: Preprint
    Format: application/pdf
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  • 7
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 81 (1998), S. 0 
    ISSN: 1551-2916
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The saturation surface of cassiterite, SnO2, was determined for liquids in the system K2O–Al2O3–SiO2 as a function of bulk composition and temperature. At fixed K2O/Al2O3 cassiterite solubility varies weakly with SiO2 concentration (76 to 84 mol%), temperature (1350° to 1550°C), and log (fO2) (−0.7 to −5.3). Cassiterite solubility is also approximately independent of composition in liquids with molar ratios of K2O/Al2O3 lessthan equal to 1 (peraluminous liquids). As K2O/Al2O3 increases from 1 (peralkaline liquids), however, cassiterite solubility increases steeply and approximately linearly with K2O in excess of Al2O3. It is proposed that potassium in excess of aluminum combines with Sn4+ to form quasi-molecular complexes with an effective stoichiometry of K4SnO4.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Earth, moon and planets 50-51 (1990), S. 57-80 
    ISSN: 1573-0794
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract Crustal formation and evolution processes are of critical importance in the geochemical and thermal evolution of planets. As an aid to understanding these processes on Venus, we develop a general paradigm for: (1) the derivation of primary magmas, and (2) the range of possible conditions for remelting of crustal materials and the evolution of the products of remelting. We use as a basis for this paradigm the present knowledge of the bulk and surface composition, thermal structure, and surface geological and geochemical processes. For the range of conditions of derivation of primary magmas and crustal remelting, a wide range of magma types is possible, and no magma type can be arbitrarily excluded from consideration on Venus. We conclude that magmatic and volcanic activity on Venus, in its broadest sense, could be very similar to that on the Earth, although eruption styles are expected to vary due to environmental conditions (Head and Wilson, 1986). Major differences in magmatic and volcanic activity are likely to occur in two environments on Venus: (1) those analogous to terrestrial island arcs, where due to the absence of water, melts should be SiO2-undersaturated, and the more fluid melt products may produce widespread deposits of SiO2-poor ferrobasalts rather than more viscous SiO2-rich magmas and composite volcanoes, and (2) those in plains regions influenced by mantle plumes and hot spots, where highly picritic melts may periodically flood vast regions of the surface.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 101 (1989), S. 326-338 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract The saturation surface of pseudobrookite (Fe2TiO5) was determined for melts in the system SiO2-Al2O3-K2O-FeO-Fe2O3-TiO2 at 1400° C and 1 atm. The variation in concentrations of Fe2O3, TiO2 and Fe2TiO5 in liquids can be used to infer relative changes in activity coefficients of these components with changing K2O/(K2O+Al2O3) of the melts. Saturation concentrations of these components are low and relatively constant in the peraluminous melts and increase with increasing K2O/(K2O+Al2O3) in peralkaline liquids. The activity coefficients of Fe2O3 and TiO2 and Fe2TiO5, therefore, are higher in peraluminous liquids than in peralkaline liquids in this system. In addition, the iron redox ratio was measured as a function of K2O/(K2O+Al2O3) for liquids just below the saturation surface; $$f_{{\text{O}}_{\text{2}} }$$ was fixed so all variations in redox ratio are entirely due to changes in melt composition. The redox ratio from unsaturated liquids was applied to saturated liquids where redox analysis of the glass is impossible. The homogeneous equilibrium experiments indicate that the activity coefficient of Fe2O3 relative to that of FeO is significantly greater in peraluminous melts than peralkaline melts. Both the heterogeneous and homogeneous equilibria suggest that in peralkaline liquids K+in excess of that required to charge balance tetrahedral Al+3 is used to stabilize both Fe+3 and Ti+4. Calculations show that ferric iron and titanium compete equally effectively for charge-balancing potassium but neither can outcompete aluminum. The observed changes in solution properties of Fe2O3 and TiO2 in the synthetic melts are used to explain variations in Fe-Ti oxide stabilities in natural peraluminous and peralkaline rhyolites and granites. Since the activity coefficients of both ferric iron and titanium are significantly higher in peraluminous liquids than in peralkaline liquids, Fe-Ti oxides should occur earlier in the crystallization sequence in peraluminous rhyolites than in peralkaline rhyolites. In addition, iron will be reduced in peraluminous granites and rhyolites relative to peralkaline ones under comparable P, T, and $$f_{{\text{O}}_{\text{2}} }$$ . Finally, observed crystallization patterns for minerals containing highly charged cations other than ferric iron and titanium are evaluated in the context of this and other experimental studies.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 138 (2000), S. 176-185 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract Partition coefficients (D) for Nb and Ta between rutile and haplogranite melts in the K2O-Al2O3-SiO2 system have been measured as functions of the K2O/Al2O3 ratio, the concentrations of Nb2O5 and Ta2O5, the temperature, in air and at 1 atmosphere pressure. The Ds increase in value as the K* [K2O/(K2O + Al2O3)] molar ratio continuously decreases from highly peralkaline [K* ∼ 0.9] to highly peraluminous [K* ∼ 0.35] melts. The D values increase more dramatically with a unit decrease in K* in peraluminous melts than in peralkaline melts. This compositional dependence of Ds can be explained by the high activity of NbAlO4 species in peraluminous melts and the high activity of KONb species (or low activity of NbAlO4 species) in peralkaline melts. A coupled substitution, Al+3 + Nb+5 (or Ta+5) = 2Ti+4, accounts for the Ds of Nb (Ta) being much greater in peraluminous melts than in peralkaline melts because this substitution allows Nb (Ta) to enter into the rutile structure more easily. The Ds of Ta between rutile and melt are greater than those of Nb at comparable concentrations because the molecular electronic polarizability of Ta is weaker than that of Nb. The Nb+5 with a large polarizing power forms a stronger covalent bond with oxygen than Ta+5 with a small polarizing power. The formation of the strong bond, Nb-O, distorts the rutile structure more severely than the weak bond, Ta-O; therefore, it is easier for Ta to partition into rutile than for Nb. These results imply that the utilization of the Nb/Ta ratio in liquid as a petrogenetic indicator in granitic melts must be done with caution if rutile (or other TiO2-rich phases) is a liquidus phase. The crystallization of rutile will increase the Nb/Ta ratio of the residual liquid because the Ds of Ta between rutile and melts are greater than those of Nb.
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