Literal solution for Hill's lunar problem     

Dieter S. Schmidt 《Celestial Mechanics and Dynamical Astronomy》1979,19(3):279-289

A computer program for the manipulation of power series in several variables is used to find the first order solution to Hill's lunar problem. The ratiom of the mean motion of the Sun to that of the Moon is kept as a formal parameter. The series inm are known to converge very poorly. It is shown how efficient algorithms among them the Lie transformation allow us to compute the series inm as far as they are needed. When the series are evaluated at Brown's numerical value form the results achieve or exceed his accuracy.  相似文献   

Preface     

Jean Chapront  Jacques Henrard  Dieter Schmidt 《Celestial Mechanics and Dynamical Astronomy》1982,26(1):2-3

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Site Correction for Long Period Seismometers, Tiltmeters and Strainmeters     

Geoffrey King  Walter Zurn  Russ Evans  Dieter Emter 《Geophysical Journal International》1976,44(2):405-411

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Exact Brans-Dicke-Bianchi types-II,VIII, and IX stiff matter solutions     

Dieter Lorenz-Petzold 《Astrophysics and Space Science》1984,98(2):281-286

Exact solutions of the Brans-Dicke field equations of Bianchi types-II, VIII, and IX are derived. The solutions represent locally rotationally symmetric universes with stiff matter content.  相似文献   

Provenance of Palaeozoic sandstones from the Carnic Alps (Austria): petrographic and geochemical indicators   总被引：1，自引：0，他引：1  

Dieter?MaderEmail author  Franz?Neubauer 《International Journal of Earth Sciences》2004,93(2):262-281

An integrated approach of petrographic analysis, whole rock geochemistry and microprobe analysis has been applied to obtain information on the geodynamic development and the provenance for Ordovician to Permian siliciclastic successions exposed within the Carnic Alps (Austria). Sandstone detrital mode and geochemical results refine previous geodynamic interpretations. Late Ordovician samples indicate a stable craton and recycled orogenic and, possible, extensional setting. The Early Carboniferous is interpreted to represent a compressional environment, followed by a Late Carboniferous molasse-type foreland basin, and a Permian extensional geodynamic setting. Contrasting geochemical patterns of post-Variscan and Permian sequences suggest a rift setting. Electron microprobe data of detrital white mica also indicate changes in the provenance. Compositional data reflect a shift from low- to medium-grade metamorphic (Ordovician) to high-grade metamorphic (Carboniferous) to low- to medium-grade metamorphic and plutonic source rocks (Permian). Additionally, our data show that various chemical discrimination diagrams do not include all possible ranges of sandstones, and that high contents of detrital mica and ultra-stable heavy minerals may cause misclassification. Consequently, we propose the use of multi-method approach for provenance studies, including the control of geochemical data by modal analysis and heavy mineral investigations.  相似文献   

SNR Surface Density Distribution in Nearby Galaxies     

Manami Sasaki  Dieter Breitschwerdt  Rodrigo Supper 《Astrophysics and Space Science》2004,289(3-4):283-286

Since supernova remnants (SNRs) are believed to be the primary sources of Galactic cosmic rays (CRs), their distribution in galaxies is an important basis for modelling and understanding the distribution of the CRs and their γ-ray spectrum. We analysed the radial surface density of X-ray and radio selected SNRs in the Large Magellanic Cloud (LMC) and M 33. Both in X-rays and in radio, the surface densities of the SNRs are in excellent agreement in both galaxies, showing an exponential decay in radius. The results were compared to the SNR distribution in the spiral galaxies M 31 and NGC 6946 as well. The radial scale length of the distribution is $\frac{1} {4} $ ? $\frac{1} {3} $ of the radius of the galaxies, fully consistent with values derived for the Milky Way, the LMC, and M 33. Therefore, not only the radio SNRs, but also the X-ray detected SNR sample can be interpreted to be representative for the CR sources within a galaxy.  相似文献   

Towards a better understanding of magnesium-isotope ratios from marine skeletal carbonates   总被引：2，自引：0，他引：2  

Dorothee Hippler  Dieter Buhl  Detlev K. Richter 《Geochimica et cosmochimica acta》2009,73(20):6134-2836

This study presents magnesium stable-isotope compositions of various biogenic carbonates of several marine calcifying organisms and an algae species, seawater samples collected from the western Dutch Wadden Sea, and reference materials. The aim of this study is to explore the influence of mineralogy, taxonomy and environmental factors (e.g., seawater isotopic composition, temperature, salinity) on magnesium-isotopic (δ²⁶Mg) ratios of skeletal carbonates. Using high-precision multi-collector inductively coupled plasma mass spectrometry, we observed that the magnesium-isotopic composition of seawater from the semi-enclosed Dutch Wadden Sea is identical to that of open marine seawater. We further found that a considerable component of the observed variability in δ²⁶Mg values of marine skeletal carbonates can be attributed to differences in mineralogy. Furthermore, magnesium-isotope fractionation is species-dependent, with all skeletal carbonates being isotopically lighter than seawater. While δ²⁶Mg values of skeletal aragonite and high-magnesium calcite of coralline red algae indicate the absence or negligibility of metabolic influences, the δ²⁶Mg values of echinoids, brachiopods and bivalves likely result from a taxon-specific level of control on Mg-isotope incorporation during biocalcification. Moreover, no resolvable salinity and temperature effect were observed for coralline red algae and echinoids. In contrast, Mg-isotope data of bivalves yield ambiguous results, which require further validation. The data presented here, point to a limited use of Mg isotopes as temperature proxy, but highlight the method’s potential as tracer of seawater chemistry through Earth’s history.  相似文献   

A high‐resolution relative time scale for the Viséan Stage (Carboniferous) of the Kulm Basin (Rhenish Mountains,Germany)     

Dieter Korn  Bernd Kaufmann 《Geological Journal》2009,44(3):306-321

The Viséan (Carboniferous) sedimentary succession of the basinal Kulm facies (Rhenish Mountains) was investigated in detail in order to achieve a high‐resolution stratigraphic subdivision and correlation. Additionally, the ranges of fossil index taxa (ammonoids), fossil marker beds, volcaniclastic horizons and sedimentary features (e.g. colour changes) were integrated in the correlation. As a result, a comprehensive database was compiled, which contains 190 stratigraphic events of the Viséan interval of this area. Several sections are almost completely composed of shales, which are regarded to represent a slow but constant basinal background sedimentation of the Kulm facies. The thickness of lithological homogeneous sections thus indicates an approximately linear record of time and the average thicknesses of biozones and positions of stratigraphic events can easily be calculated from the compiled database. The result is an approximately time‐linear biostratigraphic scale for the Viséan Stage of the Kulm Basin. Given a numerical length of the Viséan Stage of ca. 19 Ma, 190 stratigraphic events give a mean resolution of 100 000 years. This is unique in Palaeozoic stratigraphy. Copyright © 2008 John Wiley & Sons, Ltd.  相似文献   

The El Teniente porphyry Cu–Mo deposit from a hydrothermal rutile perspective     

Osvaldo M. Rabbia  Laura B. Hernández  David H. French  Robert W. King  John C. Ayers 《Mineralium Deposita》2009,44(8):849-866

Mineralogical, textural, and chemical analyses (EPMA and PIXE) of hydrothermal rutile in the El Teniente porphyry Cu–Mo deposit help to better constrain ore formation processes. Rutile formed from igneous Ti-rich phases (sphene, biotite, Ti-magnetite, and ilmenite) by re-equilibration and/or breakdown under hydrothermal conditions at temperatures ranging between 400°C and 700°C. Most rutile nucleate and grow at the original textural position of its Ti-rich igneous parent mineral phase. The distribution of Mo content in rutile indicates that low-temperature (∼400–550°C), Mo-poor rutile (5.4 ± 1.1 ppm) is dominantly in the Mo-rich mafic wallrocks (high-grade ore), while high-temperature (∼550-700°C), Mo-rich rutile (186 ± 20 ppm) is found in the Mo-poor felsic porphyries (low-grade ore). Rutile from late dacite ring dikes is a notable exception to this distribution pattern. The Sb content in rutile from the high-temperature potassic core of the deposit to its low-temperature propylitic fringe remains relatively constant (35 ± 3 ppm). Temperature and Mo content of the hydrothermal fluids in addition to Mo/Ti ratio, modal abundance and stability of Ti-rich parental phases are key factors constraining Mo content and provenance in high-temperature (≥550°C) rutile. The initial Mo content of parent mineral phases is controlled by melt composition and oxygen fugacity as well as timing and efficiency of fluid–melt separation. Enhanced reduction of SO₂-rich fluids and sulfide deposition in the Fe-rich mafic wallrocks influences the low-temperature (≤550°C) rutile chemistry. The data are consistent with a model of fluid circulation of hot (>550°C), oxidized (ƒO₂ ≥ NNO + 1.3), SO₂-rich and Mo-bearing fluids, likely exsolved from deeper crystallizing parts of the porphyry system and fluxed through the upper dacite porphyries and related structures, with metal deposition dominantly in the Fe-rich mafic wallrocks.  相似文献   

IR calibrations for water determination in olivine,r-GeO<Subscript>2</Subscript>, and SiO<Subscript>2</Subscript> polymorphs     

Sylvia-Monique?ThomasEmail author  Monika?Koch-Müller  Patrick?Reichart  Dieter?Rhede  Rainer?Thomas  Richard?Wirth  Stanislav?Matsyuk 《Physics and Chemistry of Minerals》2009,36(9):489-509

Mineral-specific IR absorption coefficients were calculated for natural and synthetic olivine, SiO₂ polymorphs, and GeO₂ with specific isolated OH point defects using quantitative data from independent techniques such as proton–proton scattering, confocal Raman spectroscopy, and secondary ion mass spectrometry. Moreover, we present a routine to detect OH traces in anisotropic minerals using Raman spectroscopy combined with the “Comparator Technique”. In case of olivine and the SiO₂ system, it turns out that the magnitude of ε for one structure is independent of the type of OH point defect and therewith the peak position (quartz ε = 89,000 ± 15,000  \textl \textmol_{\textH2\textO}^-1 \textcm^-2\text{l}\,\text{mol}_{{\text{H}_2}\text{O}}^{-1}\,\text{cm}^{-2}), but it varies as a function of structure (coesite ε = 214,000 ± 14,000  \textl \textmol_{\textH2\textO}^-1 \textcm^-2\text{l}\,\text{mol}_{{\text{H}_2}\text{O}}^{-1}\,\text{cm}^{-2}; stishovite ε = 485,000 ± 109,000  \textl \textmol_{\textH2\textO}^-1 \textcm^-2\text{l}\,\text{mol}_{{\text{H}_2}\text{O}}^{-1}\,\text{cm}^{-2}). Evaluation of data from this study confirms that not using mineral-specific IR calibrations for the OH quantification in nominally anhydrous minerals leads to inaccurate estimations of OH concentrations, which constitute the basis for modeling the Earth’s deep water cycle.  相似文献