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1.
The equilibrium in which hydrous Fe-cordierite breaks down to almandine, sillimanite, quartz, and water was previously experimentally determined by Richardson (1968) and Holdaway and Lee (1977) using QMF buffer and by Weisbrod (1973) using QIF buffer. All these studies yielded similar results — a negative dP/dT slope for the equilibrium curve. However, based on theoretical arguments, Martignole and Sisi (1981), and based on Fe-Mg partitioning experiments on coexisting cordierite and garnet in equilibrium with sillimanite and quartz, Aranovich and Podlesskii (1983) suggested that this equilibrium curve has a positive dP/dT slope and its position depends on the water content of the equilibrium cordierite. We have redetermined this equilibrium using a much improved tecnique of detecting reaction direction, and cordierite starting material that contained virtually no hercynite. Hercynite was present as a contaminant in the cordierites of previous experimental studies and possibly reacted with quartz during the experimental runs to expand the apparent stability field of Fe-cordierite. We synthesized Fe-cordierite from reagent grade oxides at 710°C and 2 kbar (using QMF buffer) with two intermediate stages of grinding and mixing. The cordierite has a unit cell volume of 1574.60 Å3 (molar volume=23.706 J/bar) and no Fe3+ as indicated by X-ray diffraction and room temperature Mössbauer studies respectively. Reaction direction was concluded by noting20% change of the ratios of intensities of two key X-ray diffraction peaks of cordierite and almandine. Our results show that the four-phase equilibrium curve passes through the points 2.1 kbar, 650°C and 2.5 kbar, 750°C. This disagrees with all previous experimental studies. H2O in the Fe-cordierite, equilibrated at 2.2 kbar and 700°C and determined by H-extraction line in the stable isotope laboratory, is 1.13 wt% (n=0.41 moles). H2O content of pure Mg-cordierite equilibrated under identical conditions and determined by thermogravimentric conditions and determined by thermogravimetric analysis is 1.22 wt% (n=0.40). Similar determinations on Fe-cordierite and Mg-cordierite equilibrated at 2.0 kbar and 650°C show 1.27 wt% (n=0.46) and 1.47 wt% (n=0.48) of H2O respectively. Thus, H2O content appears to be independent of Fe/Mg ratio in cordierite, a conclusion which supports previous experimental determinations. The experimentally determined equilibrium curve represents conditions of PH2O=Ptotal. From this we calculated the anhydrous curve representing equilibrium under conditions of X H2O V =0.0. A family of calculated equilibrium curves of constant n H2O Cord cut the experimentally determined curve at a very small angle indicating a slight variation in n H2O Cord in cordierite in equilibrium with almandine, sillimanite, and quartz under the conditions of constant X H2O V . Ancther set of calculated equilibrium curves, each representing constant a H2O V demonstrate that the slopes of the curves vary with X H2O V , and are all positive in the full range of 0.0X H2O V 1.0.  相似文献   
2.
A core from the Cambay Shale Formation of the Cambay Basin, containing immature Type III organic matter, was pyrolysed at 300°C for different durations of time to different maturation levels. Fractionation effects were studied employing a three-step extraction technique after removal of the expelled pyrolysate. The extractable organic matter (EOM) obtained on extraction of the whole core is assumed to be that present in open pores, while that obtained on finely crushing the sample is assumed to be that present in closed pores. The EOM obtained from 1 cm chips is termed EOM from semi-open pores. The gross composition of the pyrolysates expelled during pyrolysis is not similar to the oils reservoired in the area, and there is no significant fractionation observed between expelled pyrolysates and unexpelled EOM. Our study indicates movement of fluids between closed, semi-open and open pores. In both systems, there is a higher concentration of EOM in open pores than in semi-open and closed pores, and the fraction of EOM in open pores is much greater in the artificial system than in the natural system. Fractionation effects on n-alkane and isoprenoid hydrocarbon-based parameters were also studied. n-Alkenes are present in semi-open and closed pores of the immature core and in the core after it was pyrolysed to 300°C for 6 and 48 h, but are absent in the open pores. n-Alkenes are present in closed pores in the naturally matured core. Presence of n-alkenes in the pyrolysates expelled during the 6 and 48 h experiments, but their absence in the open pores of the core, indicates that expulsion also occurs through temporary microfractures during laboratory pyrolysis, whereas in the natural system expulsion from closed pores seems to be only via semi-open and open pores.  相似文献   
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Neoarchean orogenic gold deposits, associated with the greenstone-granite milieus in the Dharwar Craton include(1) the famous Kolar mine and the world class Hutti deposit;(2) small mines at HiraBuddini, Uti, Ajjanahalli, and Guddadarangavanahalli;(3) prospects at Jonnagiri; and(4) old mining camps in the Gadag and Ramagiri-Penakacherla belts. The existing diametric views on the source of ore fluid for formation of these deposits include fluids exsolved from granitic melts and extracted by metamorphic devolatilization of the greenstone sequences. Lode gold mineralization occurs in structurally controlled higher order splays in variety of host rocks such as mafic/felsic greenstones, banded iron formations, volcaniclastic rocks and granitoids. Estimated metamorphic conditions of the greenstones vary from lower greenschist facies to mid-amphibolite facies and mineralizations in all the camps are associated with distinct hydrothermal alterations. Fluid inclusion microthermometric and Raman spectroscopic studies document low salinity aqueous-gaseous(H_2O + CO_2 ± CH_4 + NaCl) ore fluids,which precipitated gold and altered the host rocks in a narrow P-T window of 0.7-2.5 kbar and 215-320℃. While the calculated fluid O-and C-isotopic values are ambiguous, S-isotopic compositions of pyrite-precipitating fluid show distinct craton-scale uniformity in terms of its reduced nature and a suggested crustal sulfur source.Available ages on greenstone metamorphism, granitoid plutonism and mineralization in the Hutti Belt are tantamount, making a geochronology-based resolution of the existing debate on the metamorphic vs.magmatic fluid source impossible. In contrast, tourmaline geochemistry suggests involvement of single fluid in formation of gold mineralization, primarily derived by metamorphic devolatilization of mafic greenstones and interlayered sedimentary rocks, with minor magmatic contributions. Similarly, compositions of scheelite, pyrite and arsenopyrite point toward operation of fault-valves that caused pressure fluctuation-induced fluid phase separation, which acted as the dominant process of gold precipitation,apart from fluid-rock sulfidation reactions. Therefore, results from geochemistry of hydrothermal minerals and those from fluid inclusion microthermometry corroborate in constraining source of ore fluid,nature of gold transport(by Au-bisulfide complex) and mechanism of gold ore formation in the Dharwar Craton.  相似文献   
5.
Factors such as non-uniform illumination of seafloor photographs and partial burial of polymetallic nodules and crusts under sediments have prevented the development of a fully automatic system for evaluating the distribution characteristics of these minerals, necessitating the involvement of a user input. A method has been developed whereby spectral signatures of different features are identified using a software ‘trained’ by a user, and the images are digitized for coverage estimation of nodules and crusts. Analysis of >20,000 seafloor photographs was carried out along five camera transects covering a total distance of 450 km at 5,100–5,300 m water depth in the Central Indian Ocean. The good positive correlation (R2 > 0.98) recorded between visual and computed estimates shows that both methods of estimation are highly reliable. The digitally computed estimates were ∼10% higher than the visual estimates of the same photographs; the latter have a conservative operator error, implying that computed estimates would more accurately predict a relatively high resource potential. The fact that nodules were present in grab samples from some locations where photographs had nil nodule coverage emphasises that nodules may not always be exposed on the seafloor and that buried nodules will also have to be accounted for during resource evaluation. When coupled with accurate positioning/depth data and grab sampling, photographic estimates can provide detailed information on the spatial distribution of mineral deposits, the associated substrates, and the topographic features that control their occurrences. Such information is critical for resource modelling, the selection of mine sites, the designing of mining systems and the planning of mining operations.  相似文献   
6.
Liquidus phase relationships in the CaAlAl–SiO6–Mg2SiO4–CaMgSi2O6–CaAlSi2O8 portion of the simplified basalt tetrahedron in the CaO–MgO–SiO2–Al2O3 system have been experimentally determined at 20 kbar pressure. The fo+di ss+sp+li univariant curve, that pierces the fo-di-an join and meets the fo+di ss+ enss+sp+li invariant point in the basalt tetrahedron, extends all the way to and pierces the di-fo-CaTs join, the limit of the simplified basalt tetrahedron toward the silica undersaturated portion.An algebraic method, relying on compositions of two successive liquids on a univariant curve and those of the crystalline phases in equilibrium with the respective liquids, is developed to identify the type of reaction that takes place along an isobarically univariant curve and to detect whether there is a temperature maximum on that curve. Use of this method for the di ss+fo+sp+li univariant equilibria shows that a temperature maximum exists on this curve at the composition Fo11Di56An3CaTs30, very close to and slighthly to the SiO2-rich side of the fo-di-CaTs join. The temperature along the univariant curve continuously decreases from the temperature maximum (1500°C) to the invariant point (1475°C) where the univariant curve is terminated by the appearance of e ss as a member of the equilibrium assemblage. Along this part of the curve, a reaction relationship occurs according to the equation fo+li=di ss+ sp. Compositions of di ss in equilibrium with the liquids from the temperature maximum to the fo+di ss+enss+ sp+li invariant point range from Di66En9CaTs25 to Di36En40CaTs24. Because of the reaction relationship of forsterite with liquid, fractional crystallization of a model alkalic basaltic liquid would cause liquids to move off the fo-di ss-sp-li univariant curve onto the sp-di ss divariant surface. Crystallization of di ss and sp would then lead to silica enrichment of residual liquids. Thus at pressures below 30 kbar, at which pressure the Al2O3–CaSiO3–MgSiO3 plane becomes a new thermal divide cutting through both the tholeiitic and alkalic volumes, alkalic liquids will fractionate toward tholeiitic compositions without crossing a thermal divide. This relationship would be expected to persist at pressures down to about 4 kbar where a maximum on the fo-di-an-li boundary line causes a thermal divide near the fo-di-an plane. Strongly SiO2-undersaturated liquids (e.g. nephelinites, basanites), on the other hand, cannot be derived from SiO2-undersaturated basalts (e.g. alkali olivine basalt) by fractional crystallization at 20 kbar. We also found that no gt primary phase volume cuts the wo-en-Al2O3 join at 20 kbar pressure. The wehrlite, the olivine clinopyroxenite, and the Al-augite group lherzolite xenoliths, containing highly aluminous clinopyroxenes (enriched in Ca-Tschermak), can be interpreted as crystal cumulates from alkalic basalts in the light of this experimental study. This is consistent with the mode of origin of these xenoliths proposed from petrographic, mineralogic, and geochemical studies.Abbreviations and notations di CaMgSi2O6 - fo Mg2SiO4 - an CaAl2Si2O8 - CaTs CaAlAlSiO6 - sp MgAl2O4 - en MgSiO3 - wo CaSiO3 - gt Ca3Al2Si3O12–Mg3Al2Si3O12 - qz SiO2 - li Liquid - gl glass - ss Solid Solution - A An mxn matrix - X A column vector - kbar kilobar  相似文献   
7.
A wavelet‐based random vibration theory has been developed for the non‐stationary seismic response of liquid storage tanks including soil interaction. The ground motion process has been characterized via estimates of statistical functionals of wavelet coefficients obtained from a single time history of ground accelerations. The tank–liquid–soil system has been modelled as a two‐degree‐of‐freedom (2‐DOF) system. The wavelet domain equations have been formulated and the wavelet coefficients of the required response state are obtained by solving two linear simultaneous algebraic equations. The explicit expression for the instantaneous power spectral density function (PSDF) in terms of the functionals of the input wavelet coefficients has been obtained. The moments of this PSDF are used to estimate the expected pseudo‐spectral acceleration (PSA) response of the tank. Parametric variations are carried out to study the effects of tank height, foundation natural frequency, shear wave velocity of soil and ratio of the mass of tank (including liquid) to the mass of foundation on the PSA responses of tanks. Copyright © 2001 John Wiley & Sons, Ltd.  相似文献   
8.
9.
The bedded felsic tuff exposed in Rutland Island, Andaman, consists of two facies:
–  white massive tuff with ill-defined bedding contacts (facies-A) and  相似文献   
10.
Application of geostatistics in estimating recoverable reserves of beach sand deposit is rare. This paper made an attempt to estimate local recoverable reserves using disjunctive kriging and discrete Gaussian model considering support and information effects for a beach sand deposit located in the eastern part of India. The dependence of different selective mining unit (SMU) sizes and different production sampling strategies on the estimated tonnage, metal quantity, and the ore tonnage versus metal quantity relationships has been examined. The results of the study show that nonlinear geostatistics should be used for more precise assessment of the grade, ore tonnage, and metal quantity and their relationships, which are necessary for recoverable reserve estimation. In selective mining operation, both support and information effects have significant influence on recoverable reserve. Recoverable reserve estimation based on SMU involves estimating grade distributions of mining unit with much bigger support than the available drill core sample data. Information effect comes into picture from the real scenario where the actual grades of the blocks remain unknown even during mining. At the mining stage, discrimination of ore and waste blocks is carried out based on estimated grades of the production samples and it is likely that the blocks might be misclassified as either ore or waste and thus sent to wrong destination. Information effect modeling makes the estimation more reliable by taking care of misclassification.  相似文献   
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