Geochemistry of Coexisting Biotite and Muscovite of Portuguese Peraluminous Granitic Differentiation Series     

A.M.R. Neiva  M.M.V.G. Silva  M.E.P. Gomes  T.F.C. Campos 《Chemie der Erde / Geochemistry》2002,62(3):197-215

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Structural relaxation in the MnCO3–CaCO3 solid solution: a Mn K-edge EXAFS study     

Y. J. Lee  R. J. Reeder  R. W. Wenskus  E. J. Elzinga 《Physics and Chemistry of Minerals》2002,29(9):585-594

Mn K-edge EXAFS spectroscopy of solid-solution samples encompassing the complete MnCO₃–CaCO₃ series shows that first-shell Mn–O distances deviate little from the 2.19-Å distance observed in pure MnCO₃. Very slight lengthening is observed only in the limiting case of dilute Mn(II) calcite solid solutions, where the Mn–O distance is 2.21 Å. The observed nearly complete structural relaxation and the composition independence of the Mn–O distance are consistent with the Pauling model behavior of solid solutions, and agree with previous studies showing a high degree of relaxation around hetero-sized substituents in the calcite structure. Strain occurs through bond bending, which is facilitated by the exclusively corner-sharing topology of calcite. Observed distances from Mn to more distant neighbors show significant variation across the solid-solution series that resembles Vegard's law-type behavior but reflects averaging. The high degree of relaxation suggests modest enthalpies of mixing in the solution, consistent with calorimetric studies.  相似文献   

有限弹性变形地壳中的地震波     

范家参 《地震研究》2002,25(1):48-52

地壳由半无限大的基岩上一层厚度为H^-的表土层组成，入射地震波为垂直的SH波，产生水平地面运动。当浅源大地震发生时，在极震区以外行波传播产生地面运动将使地壳介质有非线性的有限弹性变形。用小参数摄动法使非线性控制方程为线性化的小参数各阶控制方程，得出头两阶线性控制方程的解析解。  相似文献   

Chemical equilibria of thermal waters for the application of geothermometers from the Guanzhong basin, China     

Zheng Xilai  Halldor Armannsson  Li Yongle  Qiu Hanxue 《Journal of Volcanology and Geothermal Research》2002,113(1-2)

In this study, representative samples from thermal wells and springs were chemically analyzed and geothermometers were used to calculate the deep temperatures of geothermal reservoirs on the basis of water–mineral equilibrium. In some cases, however, the chemical components are not in equilibrium with the minerals in the reservoir. Therefore, log(Q/K) diagrams are used to study the chemical equilibrium for the minerals that are likely to participate. The Na–K–Mg triangular diagram is also applied to evaluate the equilibrium of water with reservoir rocks. Standard curves at the reference temperatures are prepared to reveal which type of silica geothermometer is appropriate for the specified condition. This study shows that water samples from geothermal wells W9 and W12 are in equilibrium with the selective minerals, and chalcedony may control the fluid–silica equilibrium. It is estimated that there is an exploitable low-temperature reservoir with possible temperatures of 80–90°C in the Guanzhong basin.  相似文献   

姑山铁矿东帮河堤的稳定性分析     

林海  陈征宙  孙斌堂  陈为伟 《华东地质学院学报》2003,26(2):187-191

基于极限平衡理论，采用以简化毕肖普法为主，费伦纽斯法作为参照的分析方法，对姑山铁矿采矿场东帮及青山河河堤防渗加固后的稳定性进行了分析评价，根据不同的爆破震动大小，得出背水面和迎水面多个安全系数值，取得了较为可靠的分析结果。  相似文献   

含矿流体混合反应与成矿作用的动力平衡模拟研究   总被引：7，自引：0，他引：7  

林舸  CBZHAO  王岳军  BEHOBBS  龚纪文 《岩石学报》2003,19(2):275-282

本文在约定热液体系中成矿元素成矿速率(成矿过程中单位时间内单位体积所合成矿元素重量的变化)的基础上。借助于物质-热-化学-成矿四重全耦合的研究思路，构建了均匀热液体系、层状热液体系、岩浆侵入热液体系下成矿元素的迁移、富集、溶解与沉淀作用数值模型。模拟结果表明；(1)硫化物(H2S)和硫酸盐(SO42-)流体的混合反应是成矿热液体系中铅、锌、铁成矿元素成矿的重要控制因素；(2)均匀介质、岩浆侵入或地质构造的存在，对成矿元素在成矿流体运移的速度、流线、温度分布和成矿元素的溶解与沉淀分布都有着各自的特征．不同的成矿环境或成矿背景制约了成矿元素的迁移与富集以及矿体的产出定位。暗示成矿环境及成矿速率对热液体系中成矿元素的沉淀与溶解具重要作用；成矿流体的混合反应是成矿作用发生的重要机制之一。在成矿理论研究中必须充分考虑不同地质构造因素的约束。  相似文献   

正常椭球内部场的内蕴几何与密度分布     

黄金水 《武汉大学学报(信息科学版)》1997,(4)

将重力场内蕴几何结构的研究引入到正常椭球内部场的研究中，深入探讨了内蕴几何量及其与内部物理量之间的关系，并据此建立了弱平衡条件下的基本微分方程，进而给出确定椭球内部内蕴几何量与场源密度分布的方法。研究表明，平衡形状理论中的Ｗａｖｒｅ公式和Ｃｌａｉｒａｕｔ方程可由内蕴几何与内部物理量之间的关系导出，它们是在平衡假设下取椭球近似的结果。  相似文献   

橄榄岩中尖晶石的O同位素继承性与晶体结构转换     

李一良  王峥嵘  郑永飞 《地球学报》1997,18(Z1):260-262

应用增量法计算的矿物对O同位素分馏曲线，得到正尖晶石-矿物对O同位素温度高于尖晶石在地幔中的熔点，而用反尖晶石-矿物对计算的O同位素温度低于尖晶石的熔点，较为合理。因此，地幔橄榄岩中镁铝尖晶石的O同位素组成可能继承了其母体反尖晶石特征，即使反结构尖晶石在发生相变作用变成正结构尖晶石时未发生O同位素再平衡。  相似文献   

Disequilibrium for Ca during growth of pelitic garnet   总被引：14，自引：1，他引：14  

C. B. CHERNOFF  & W. D. CARLSON 《Journal of Metamorphic Geology》1997,15(4):421-438

Compositional zoning in hundreds of almandine-rich garnets in amphibolite by facies micaceous quartzites from the Picuris Range, north-central New Mexico USA, indicates that although Mn, Mg and Fe achieve chemical equilibrium at hand-sample scale during garnet growth, Ca does not. Instead, Ca concentrations at the surface of growing garnets appear to depend strongly on kinetic factors that govern the local chemical environment, yielding disequilibrium for Ca at scales larger than the region immediately surrounding an individual porphyroblast. Detailed zoning profiles were obtained for 371 garnet crystals in a small volume of a single sample of garnetiferous quartzite, and core analyses were made of 97 additional crystals. Each analysis was made on a section that passed precisely through the morphological centre of the crystal, located by means of 3-D imagery from computed X-ray tomography. The data reveal strong correlations between crystal size and concentrations of Mn, Mg and Fe (but not Ca) in garnet cores; a relationship between crystal size and isolation; rigorous cross-correlations among concentrations of Mn, Mg and Fe (but not Ca); and systematic variations in Ca concentrations as a function of crystal size and core composition that are anomalous in comparison to the behaviour of the other divalent cations. We interpret these observations as the result of thermally accelerated diffusion-controlled garnet growth, in circumstances that promoted rapid intergranular diffusion and thus rock-wide equilibration of Mn, Mg and Fe, but that prevented equilibration at similar scale for Ca because of its more sluggish intergranular diffusion. The anomalous behaviour of Ca is made evident in these garnets by the presence of sharp spikes in Ca concentration, which are demonstrably not a consequence of any simultaneous rock-wide event, such as a change in pressure, temperature, or some other intensive parameter. Instead, Ca concentrations probably reflect the local extent of reaction in the immediate vicinity of each porphyroblast. To the degree that such kinetic factors introduce departures from chemical equilibrium for Ca, thermobarometric estimates that involve grossular contents of pelitic garnet will be in error.  相似文献   

A ternary solid solution model for omphacite and its application to geothermobarometry of eclogites from the Middle Adula nappe (Central Alps, Switzerland)   总被引：7，自引：0，他引：7  

C. MEYRE  C. DE CAPITANI  & J. H. PARTZSCH 《Journal of Metamorphic Geology》1997,15(6):687-700

A ternary solid solution model for omphacite with the end-members jadeite (NaAlSi₂O₆), diopside (CaMgSi₂O₆) and hedenbergite (CaFeSi₂O₆) was derived from experimental data from the literature. The subregular solution model, fitted by linear programming, is best suited to omphacites with very little aegirine component in common eclogites. Applying this solution model to the calculation of equilibrium phase diagrams of eclogites from the Adula nappe (Central Alps, Switzerland) results in large stability fields for common eclogite assemblages (garnet+omphacite+quartz+H₂O±kyanite). Within this field the compositions of garnet and omphacite show very little variation. A precise determination of the peak-pressure and temperature is not possible. The occurrence of amphibole, overgrowing the peak-pressure assemblage in fresh eclogite, suggests retrograde re-equilibration, still under eclogite facies conditions. The computation of isopleths for garnet and pyroxene end-members allows the estimation of the pressure and temperature conditions of this re-equilibration event (19–21  kbar, c .  700 °C).  相似文献