Channel water balance of the Lena River Cascade system     

N. E. Kosheleva  E. B. Karabanov  N. S. Kasimov  A. G. Kositskii  V. A. Bychinskii  D. Williams  S. Armstrong 《Doklady Earth Sciences》2006,411(9):1452-1456

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The early cretaceous collisional granite-leucogranite association of the Stanovoi Terrane: New geochronological, geochemical, and isotope-geochemical data     

V. E. Strikha  N. I. Rodionov 《Doklady Earth Sciences》2006,406(1):107-111

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Hydrogeology of thermal waters in Viterbo area, central Italy     

V. Piscopo  M. Barbieri  V. Monetti  G. Pagano  S. Pistoni  E. Ruggi  D. Stanzione 《Hydrogeology Journal》2006,14(8):1508-1521

A conceptual hydrogeological model of the Viterbo thermal area (central Italy) has been developed. Though numerous studies have been conducted on its geological, geochemical and geothermal features, there is no generalized picture defining the origin and yield of the hydrothermal system. These latter aspects have therefore become the objectives of this research, which is based on new hydrogeological and geochemical investigations. The geological setting results in the coexistence of overlapped interacting aquifers. The shallow volcanic aquifer, characterized by fresh waters, is fed from the area around the Cimini Mountains and is limited at its base by the semiconfining marly-calcareous-arenaceous complex and low-permeability clays. To the west of Viterbo, vertical upflows of thermal waters of the sulphate-chloride-alkaline-earth type with higher gas contents, are due to the locally uplifted carbonate reservoir, the reduced thickness of the semiconfining layer and the high local geothermal gradient. The hot waters (30–60°C) are the result of deep circulation within the carbonate rocks (0.5–1.8 km) and have the same recharge area as the volcanic aquifer. The upward flow in the Viterbo thermal area is at least 0.1 m³/s. This flow feeds springs and deep wells, also recharging the volcanic aquifer from below.  相似文献   

New data on hydrocarbons in auriferous conglomerates of the Witwatersrand ore region, Republic of South Africa     

A. A. Kremenetsky  I. E. Maksimyuk 《Lithology and Mineral Resources》2006,41(2):102-116

Genesis of deposits in the world’s largest Witwatersrand auriferous region (South Africa) remains a debatable issue over several decades. Based on geological and mineralogical-geochemical investigations, we previously proposed a sedimentary-exhalative hypothesis for its origin. In the present communication, we have attempted to develop and scrutinize this concept based on the study of organic matter in ore and nonore conglomerates, quartz in conglomerate pebbles, and fluid inclusions in quartz from pebbles and cement of ore and nonore conglomerates.  相似文献   

Different-depth xenoliths from Devonian intrusions of the Kola peninsula: Key to deciphering paleogeodynamic settings of alkaline magmatism     

A. S. Baluev  E. N. Terekhov 《Doklady Earth Sciences》2006,407(2):167-171

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Lower Miocene sediments of central and western Ciscaucasia     

A. S. Stolyarov  E. I. Ivleva 《Lithology and Mineral Resources》2006,41(2):174-186

The composition, structure, and geochemical properties of the thickest, relatively deep-water Lower Miocene sediments developed in western Ciscaucasia are considered. Of particular interest are materials from the Kuban superdeep borehole SG-12000 that recovered the uppermost layers of the Maikop Group at 3148–3961 m in the central Indol-Kuban Trough west of Krasnodar. However, the borehole did not penetrate the whole Lower Miocene section of the Maikop Group. Therefore, characteristics of the Maikop Group are supplemented with new materials from several other boreholes drilled in the eastern Kuban region. Thus, the typical (reference) Lower Miocene section of central and western Ciscaucasia has been sufficiently well described.  相似文献   

Equation of state of MgGeO3 perovskite to 65 GPa: comparison with the post-perovskite phase     

C. E. Runge  A. Kubo  B. Kiefer  Y. Meng  V. B. Prakapenka  G. Shen  R. J. Cava  T. S. Duffy 《Physics and Chemistry of Minerals》2006,33(10):699-709

The equation of state of MgGeO₃ perovskite was determined between 25 and 66 GPa using synchrotron X-ray diffraction with the laser-heated diamond anvil cell. The data were fit to a third-order Birch–Murnaghan equation of state and yielded a zero-pressure volume (V ₀) of 182.2 ± 0.3 Å³ and bulk modulus (K ₀) of 229 ± 3 GPa, with the pressure derivative (K′₀ = (?K ₀/?P) _T ) fixed at 3.7. Differential stresses were evaluated using lattice strain theory and found to be typically less than about 1.5 GPa. Theoretical calculations were also carried out using density functional theory from 0 to 205 GPa. The equation of state parameters from theory (V ₀ = 180.2 Å³, K ₀ = 221.3 GPa, and K′₀ = 3.90) are in agreement with experiment, although theoretically calculated volumes are systematically lower than experiment. The properties of the perovskite phase were compared to MgGeO₃ post-perovskite phase near the observed phase transition pressure (～65 GPa). Across the transition, the density increased by 2.0(0.7)%. This is in excellent agreement with the theoretically determined density change of 1.9%; however both values are larger than those for the (Mg,Fe)SiO₃ phase transition. The bulk sound velocity change across the transition is small and is likely to be negative [?0.5(1.6)% from experiment and ?1.2% from theory]. These results are similar to previous findings for the (Mg,Fe)SiO₃ system. A linearized Birch–Murnaghan equation of state fit to each axis yielded zero-pressure compressibilities of 0.0022, 0.0009, and 0.0016 GPa^?1 for the a, b, and c axis, respectively. Magnesium germanate appears to be a good analog system for studying the properties of the perovskite and post-perovskite phases in silicates.  相似文献   

Geochemistry and formation conditions of rare-metal granites with various fluorine-bearing minerals (fluorite,topaz, and cryolite)     

V. S. Antipin  E. A. Savina  M. A. Mitichkin 《Geochemistry International》2006,44(10):965-975

A comparative geochemical study of rare-metal granitoids with various fluorine-bearing minerals (fluorite, topaz, and cryolite) was carried out. It was shown that these rocks correspond to both plumasitic and agpaitic geochemical types. The fluorite-, topaz-, and cryolite-bearing granites of these geochemical types are distinctly different in geochemical parameters and the character of magmatic evolution. These differences are related to the composition of initial magmas and their sources. Rare-metal granitoids with fluorine-bearing minerals compose small massifs, stocks, and dike swarms. Their formation is independent of the composition and age of the country rocks or geologic structures where they occur. Original Russian Text ? V.S. Antipin, E.A. Savina, M.A. Mitichkin, 2006, published in Geokhimiya, 2006, No. 10, pp. 1040–1052.  相似文献   

Secular variations of the upper crust composition: Implication of geochemical data on the Upper Precambrian shales from the Southern Urals western flank and Uchur-Maya region     

A. V. Maslov  V. N. Podkovyrov  Yu. L. Ronkin  M. T. Krupenin  E. Z. Gareev  V. M. Gorozhanin 《Stratigraphy and Geological Correlation》2006,14(2):126-149

In the mid-1980s, it was concluded based on geochemical study that Th, Sc, La concentrations and ratios Th/Sc, La/Sc and Eu/Eu* did not wary significantly in the post-Archean time. It was impossible to judge about compositional variations of upper crust during the Riphean and Vendian, because data of that time characterized a limited number of samples from the post-Archean basins of Australia, New Zealand, and Antarctic. Considered in this work are variations of Eu/Eu*, LREE/HREE, Th/Sc, and La/Sc ratios in Upper Precambrian fine-grained siliciclastic rock of the Southern Urals western flank (Bashkirian meganticlinorium) and Uchur-Maya region (Uchur-Maya plate and Yudoma-Maya belt). As is established, only the Eu anomaly in the studied siliciclastic rocks is practically identical to this parameter of the average post-Archean shale. Three other parameters plot on the Riphean-Vendian variation curves with positive and negative excursions of diverse magnitude, which do not coincide always in time. It is assumed that these excursions likely mark stages of local geodynamic activity, destruction of pre-Riphean cratons, and progressing recycling of sedimentary material during the Riphean.  相似文献   

New data on Sr-and C-isotopic chemostratigraphy of the Upper Riphean type section (Southern Urals)     

A. B. Kuznetsov  M. A. Semikhatov  A. V. Maslov  I. M. Gorokhov  E. M. Prasolov  M. T. Krupenin  I. V. Kislova 《Stratigraphy and Geological Correlation》2006,14(6):602-628

New data on Sr-and C-isotopic systematics of carbonate rocks from the Upper Riphean stratotype (Karatau Group of the southern Urals) are obtained for several southwestern sections of the Bashkirian meganticlinorium, which have not been studied before. The results obtained supplement the Sr-and C-isotopic information for the group upper horizons thus detailing chemostratigraphic characterization of the entire succession. Limestone and dolostone samples used to analyze the Sr isotope composition satisfy strict geochemical criteria of the isotopic system retentivity and have been subjected to preliminary treatment in ammonium acetate to remove secondary carbonate phases. Data on 255 samples of carbonate rocks (171 studied for the first time) show that δ¹³C value varies in the Karatau Group succession from ?2.8 to +5.9 ‰ V-PDB with several in-phase excursions from the general trend in all the sections studied in the area 90 × 130 km. The δ¹³C variation trend demarcates several levels in the carbonate succession of the Karatau Group suitable for objectives of regional stratigraphy and for C-isotope chemostratigraphic subdivision of the Upper Riphean. The results of Sr isotopic analysis of 121 samples (51 unstudied before) from the Karatau Group imply that rocks in its lower part (the Katav Formation and basal horizon of the Inzer Formation) experienced considerable secondary alterations, while limestones and dolostones of the overlying interval of the group are frequently unaltered. In the “best” samples satisfying geochemical criteria of the isotopic system retentivity, the ⁸⁷Sr/⁸⁶Sr initial ratio increases from 0.70521–0.70532 in the lower Inzer deposits to 0.70611 in the upper Min’yar carbonates, decreasing to <0.70600 near the top of the latter. Above the regional hiatus separating the Min’yar and Uk formation, this ratio grows from 0.70533 to 0.70605–0.70609 in the limestone succession of the last formation.  相似文献