Abstracts of papers held at the IMA symposium physics of minerals,novosibirsk, USSR, 1978 (appendix)     

K. Langer  John K. Winter  Fujio P. Okamura  Subrata Ghose 《Physics and Chemistry of Minerals》1979,4(1):101-103

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Accuracy of mean gravity anomalies obtained from point and profile measurements     

H. Moritz 《Journal of Geodesy》1966,40(2):157-169

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Optical absorption and mössbauer spectra of purple and green yoderite,a kyanite-related mineral     

R. M. Abu-Eid  K. Langer  F. Seifert 《Physics and Chemistry of Minerals》1978,3(3):271-289

Mössbauer and polarized optical absorption spectra of the kyanite-related mineral yoderite were recorded. Mössbauer spectra of the purple (PY) and green yoderite (GY) from Mautia Hill, Tanzania, show that the bulk of the iron is Fe³⁺ in both varieties, with Fe²⁺/(Fe²⁺+Fe³⁺) ratios near 0.05. Combining this result with new microprobe data for PY and with literature data for GY gives the crystallochemical formulae: $$\begin{gathered} ({\text{Mg}}_{{\text{1}}{\text{.95}}} {\text{Fe}}_{{\text{0}}{\text{.02}}}^{{\text{2 + }}} {\text{Mn}}_{{\text{0}}{\text{.01}}}^{{\text{2 + }}} {\text{Fe}}_{{\text{0}}{\text{.34}}}^{{\text{3 + }}} {\text{Mn}}_{{\text{0}}{\text{.07}}}^{{\text{3 + }}} {\text{Ti}}_{{\text{0}}{\text{.01}}} {\text{Al}}_{{\text{3}}{\text{.57}}} )_{5.97}^{[5,6]} \hfill \\ {\text{Al}}_{{\text{2}}{\text{.00}}}^{{\text{[5]}}} [({\text{Si}}_{{\text{3}}{\text{.98}}} {\text{P}}_{{\text{0}}{\text{.03}}} ){\text{O}}_{{\text{18}}{\text{.02}}} ({\text{OH)}}_{{\text{1}}{\text{.98}}} ] \hfill \\ \end{gathered}$$ and PY and $$\begin{gathered} ({\text{Mg}}_{{\text{1}}{\text{.98}}} {\text{Fe}}_{{\text{0}}{\text{.02}}}^{{\text{2 + }}} {\text{Mn}}_{{\text{< 0}}{\text{.001}}}^{{\text{2 + }}} {\text{Fe}}_{{\text{0}}{\text{.45}}}^{{\text{3 + }}} {\text{Ti}}_{{\text{0}}{\text{.01}}} {\text{Al}}_{{\text{3}}{\text{.56}}} )_{6.02}^{[5,6]} \hfill \\ {\text{Al}}_{{\text{2}}{\text{.00}}}^{{\text{[5]}}} [({\text{Si}}_{{\text{3}}{\text{.91}}} {\text{O}}_{{\text{17}}{\text{.73}}} {\text{(OH)}}_{{\text{2}}{\text{.27}}} ] \hfill \\ \end{gathered}$$ for GY. The Mössbauer spectra at room temperature contain one main doublet with isomer shifts and quadrupole splittings of 0.36 (PY), 0.38 (GY) and 1.00 (PY), 0.92 (GY) mm s^?1, respectively. These values correspond to Fe³⁺ in six or five-fold coordination. The doublet components have anomalously large half widths indicating either accomodation of Fe³⁺ in more than one position (e.g., octahedraA1 and five coordinatedA2) or the yet unresolved superstructure. Besides strong absorption in the ultraviolet (UV) starting from about 25,000 cm^?1, the polarized optical absorption spectra are dominated by strong bands around 16,500 and 21,000 cm^?1 (PY) and a medium strong band at around 13,800 cm^?1 (GY). Position and polarization of these bands, in combination with the UV absorption, explain the colour and pleochroism of the two varieties. The bands in question are assigned to homonuclear metal-to-metal charge transfer transitions: Mn²⁺(A1) Mn³⁺(A1′) ? Mn³⁺(A1) Mn²⁺(A1′) and Mn²⁺(A1) Mn³⁺(A2 ? Mn³⁺(A1) Mn²⁺(A2) in PY and Fe²⁺(A1) Fe³⁺(A1′) ? Fe³⁺(A1) Fe²⁺(A1′) in GY. The evidence for homonuclear Mn²⁺ Mn³⁺ charge transfer (CTF) is not quite clear and needs further study. Heteronuclear FeTi CTF does not contribute to the spectra. In PY, additional weak bands were resolved at energies around 17,700, 18,700, 21,000, and 21,900 cm^?1 and assigned to Mn³⁺ in two positions. Weak bands around 10,000 cm^?1 in both varieties are assigned to Fe²⁺ spin-alloweddd-transitions. Very weak and sharp bands, around 15,400, 16,400, 21,300, 22,100, 23,800, and 25,000 cm^?1 are identified in GY and assigned to Fe³⁺ spin-forbiddendd-transitions.  相似文献   

Synthesis and stability of deerite,Fe 12 2+ Fe 6 3+ [Si12O40](OH)10, and Fe3+⇋Al3+ substitutions at 15–28 kb     

K. Langer  D. Lattard  W. Schreyer 《Contributions to Mineralogy and Petrology》1977,60(3):271-297

Deerite, Fe ₁₂ ²⁺ Fe ₆ ³⁺ [Si₁₂O₄₀](OH)₁₀, thus far known from ten localities in glaucophane schist terranes, was synthesized at water pressures of 20–25 kb and temperatures of 550–600 °C under the of the Ni/NiO buffer. The X-ray powder diagram, lattice constants and infrared spectrum of the synthetic phase are closely similar to those of the natural mineral. A solid solution series extends from this ferri-deerite end member to some 20 mole % of a hypothetical alumino-deerite, Fe ₁₂ ²⁺ Al ₆ ³⁺ [Si₁₂O₄₀](OH)₁₀. The upper temperature breakdown of ferri-deerite to the assemblage ferrosilite +magnetite+quartz+water occurs at about 490 °C at 15 kb, and 610 °C at 25 kb fluid pressure for the of the Ni/NiO buffer. Extrapolation of these data to lower water pressures indicates that deerite can be a stable mineral only in very low-temperature, high-pressure environments.  相似文献   

Stable Cu and Zn isotope ratios as tracers of sources and transport of Cu and Zn in contaminated soil   总被引：7，自引：0，他引：7  

Moritz Bigalke  Stefan Weyer  Jozef Kobza 《Geochimica et cosmochimica acta》2010,74(23):6801-6813

Copper and Zn metals are produced in large quantities for different applications. During Cu production, large amounts of Cu and Zn can be released to the environment. Therefore, the surroundings of Cu smelters are frequently metal-polluted. We determined Cu and Zn concentrations and Cu and Zn stable isotope ratios (δ⁶⁵Cu, δ⁶⁶Zn) in three soils at distances of 1.1, 3.8, and 5.3 km from a Slovak Cu smelter and in smelter wastes (slag, sludge, ash) to trace sources and transport of Cu and Zn in soils. Stable isotope ratios were measured by multicollector inductively coupled plasma mass spectrometry (MC-ICP-MS) in total digests. Soils were heavily contaminated with concentrations up to 8087 μg g⁻¹ Cu and 2084 μg g⁻¹ Zn in the organic horizons. The δ⁶⁵Cu values varied little (−0.12‰ to 0.36‰) in soils and most wastes and therefore no source identification was possible. In soils, Cu became isotopically lighter with increasing depth down to 0.4 m, likely because of equilibrium reactions between dissolved and adsorbed Cu species during transport of smelter-derived Cu through the soil. The δ⁶⁶Zn_IRMM values were isotopically lighter in ash (−0.41‰) and organic horizons (−0.85‰ to −0.47‰) than in bedrock (−0.28‰) and slag (0.18‰) likely mainly because of kinetic fractionation during evaporation and thus allowed for separation of smelter-Zn from native Zn in soil. In particular in the organic horizons large variations in δ⁶⁶Zn values occur, probably caused by biogeochemical fractionation in the soil-plant system. In the mineral horizons, Zn isotopes showed only minor shifts to heavier δ⁶⁶Zn values with depth mainly because of the mixing of smelter-derived Zn and native Zn in the soils. In contrast to Cu, Zn isotope fractionation between dissolved and adsorbed species was probably only a minor driver in producing the observed variations in δ⁶⁶Zn values. Our results demonstrate that metal stable isotope ratios may serve as tracer of sources, vertical dislocation, and biogeochemical behavior in contaminated soil.  相似文献   

Architecture of Upper Cretaceous rhyodacitic hyaloclastite at the polymetallic Madneuli deposit,Lesser Caucasus,Georgia     

Nino Popkhadze  Robert Moritz  Vladimer Gugushvili 《Central European Journal of Geosciences》2014,6(3):308-329

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The effects of vigorous mixing in a convective model of zonal flow on the ice giants     

Jonathan Aurnou  Moritz Heimpel 《Icarus》2007,190(1):110-126

Previous studies have used models of three-dimensional (3D) Boussinesq convection in a rotating spherical shell to explain the zonal flows on the gas giants, Jupiter and Saturn. In this paper we demonstrate that this approach can also generate flow patterns similar to those observed on the ice giants, Uranus and Neptune. The equatorial jets of Uranus and Neptune are often assumed to result from baroclinic cloud layer processes and have been simulated with shallow layer models. Here we show that vigorous, 3D convection in a spherical shell can produce the retrograde (westward) equatorial flows that occur on the ice giants as well as the prograde (eastward) equatorial flows of the gas giants. In our models, the direction of the equatorial jet depends on the ratio of buoyancy to Coriolis forces in the system. In cases where Coriolis forces dominate buoyancy, cylindrical Reynolds stresses drive prograde equatorial jets. However, as buoyancy forces approach and exceed Coriolis forces, the cylindrical nature of the flow is lost and 3D mixing homogenizes the fluid's angular momentum; the equatorial jet reverses direction, while strong prograde jets form in the polar regions. Although the results suggest that conditions involving strong atmospheric mixing are responsible for generating the zonal flows on the ice giants, our present models require roughly 100 and 10 times the internal heat fluxes observed on Uranus and Neptune, respectively.  相似文献   

Timing of igneous accretion,composition, and temporal relation of the Kassandra–Sithonia rift-spreading center within the eastern Vardar suture zone,Northern Greece: insights into Jurassic arc/back-arc systems evolution at the Eurasian plate margin     

Nikolay Bonev  Peter Marchev  Robert Moritz  Petyo Filipov 《International Journal of Earth Sciences》2015,104(7):1837-1864

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Optical absorption spectroscopy of Cr3+-ions in phyllosilicates     

A. N. Platonow  K. Langer  G. Calas  M. Andrut 《Physics and Chemistry of Minerals》1996,23(4-5):241-242

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An equation of state at subnuclear densities     

William D. Langer  Leonard C. Rosen  Jeffrey M. Cohen  A. G. W. Cameron 《Astrophysics and Space Science》1969,5(3):259-271

An equation of state for cold matter above white dwarf densities is evaluated. The gas is considered to be a mixture of degenerate neutrons, protons and electrons combined with nuclei of one type (that is only oneA andZ value). We derive the equilibrium equations for the mixture and calculate the number densities as well as theA andZ of the nucleus. Finally we calculate an equation of state, which smoothly goes over to that of a neutron, proton electron gas mixture at a density of 5×10¹³ g/cm³.  相似文献