An experimental study of the grain-scale processes of peridotite melting: implications for major and trace element distribution during equilibrium and disequilibrium melting   总被引：1，自引：0，他引：1  

Mauro Lo Cascio  Yan Liang  Nobumichi Shimizu  Paul C. Hess 《Contributions to Mineralogy and Petrology》2008,156(1):87-102

The grain-scale processes of peridotite melting were examined at 1,340°C and 1.5 GPa using reaction couples formed by juxtaposing pre-synthesized clinopyroxenite against pre-synthesized orthopyroxenite or harzburgite in graphite and platinum-lined molybdenum capsules. Reaction between the clinopyroxene and orthopyroxene-rich aggregates produces a melt-enriched, orthopyroxene-free, olivine + clinopyroxene reactive boundary layer. Major and trace element abundance in clinopyroxene vary systematically across the reactive boundary layer with compositional trends similar to the published clinopyroxene core-to-rim compositional variations in the bulk lherzolite partial melting studies conducted at similar P–T conditions. The growth of the reactive boundary layer takes place at the expense of the orthopyroxenite or harzburgite and is consistent with grain-scale processes that involve dissolution, precipitation, reprecipitation, and diffusive exchange between the interstitial melt and surrounding crystals. An important consequence of dissolution–reprecipitation during crystal-melt interaction is the dramatic decrease in diffusive reequilibration time between coexisting minerals and melt. This effect is especially important for high charged, slow diffusing cations during peridotite melting and melt-rock reaction. Apparent clinopyroxene-melt partition coefficients for REE, Sr, Y, Ti, and Zr, measured from reprecipitated clinopyroxene and coexisting melt in the reactive boundary layer, approach their equilibrium values reported in the literature. Disequilibrium melting models based on volume diffusion in solid limited mechanism are likely to significantly underestimate the rates at which major and trace elements in residual minerals reequilibrate with their surrounding melt. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

Re-Os dating of molybdenite from the Hukeng tungsten deposit in the Wugongshan area, Jiangxi Province, and its geological implications   总被引：1，自引：0，他引：1  

LIU Jun  YE Huishou  XIE Guiqing  YANG Guoqiang  ZHANG Wei 《地质学报》2008,82(11)

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Simple models for dynamic melting in an upwelling heterogeneous mantle column: Analytical solutions     

Yan Liang 《Geochimica et cosmochimica acta》2008,72(15):3804-3821

Several lines of evidence suggest that the melt generation and segregation regions of the mantle are heterogeneous, consisting of chemically and lithologically distinct domains of variable size and dimension. Partial melting of such heterogeneous mantle source regions gives rise to a diverse range of basaltic magmas. In order to better assess the role of source heterogeneity during mantle melting, we have undertaken a theoretical study of trace element distribution and fractionation during concurrent melting and melt migration in an upwelling, chemically heterogeneous, two-porosity double lithology melting column. Analytical solutions for the abundance of a trace element in the matrix and channel were obtained under the assumptions that the porosity, melt and solid velocities, and solid-melt partition coefficients are constant and uniform. For simplicity, we neglected diffusion and dispersion in the melt. Chemical source heterogeneities of arbitrary size and shape were integrated into the simple melting models by allowing trace element abundance in the source region to vary as a function of time and space. Concurrent melting and melt migration in an upwelling heterogeneous mantle may be approximated as a quasi-steady state problem in which time-dependent concentration patterns produced by melting of heterogeneous source regions are superimposed on a reference steady-state concentration distribution established by melting of the ambient or background mantle. Chromatographic fractionation is especially important for the matrix melt and solid when chemical heterogeneities are involved during melting and melt migration in the mantle, giving rise to significant phase-shift between two incompatible trace elements in the matrix melt and scattered correlations among incompatible trace elements in residual peridotites. Mixing is the chief mass transfer process in the dunite channel where the chromatographic effect is negligible for most of the incompatible trace elements. The lack of chromatographic fractionation among incompatible trace elements and isotopic ratios in MORB suggests either most MORB are channel melts or mixing in magma conduit and chamber is very efficient such that the phase-shift is averaged out during magma transport and storage processes. Advection brings melt produced by smaller-degree of melting in the deeper part of the melting column to the overlying melting region, increasing the incompatible trace element abundance in the matrix and the channel. This advection-induced self-enrichment is especially important when heterogeneous sources are involved and may account for some of the enriched incompatible trace element patterns observed in residual peridotite that were previously interpreted to be a result of mantle metasomatism. Systematic studies of high-resolution spatially correlated mantle samples may help to constrain the melting history and the size and nature of chemical heterogeneities in the mantle.  相似文献   

Considerations for conducting incubations to study the mechanisms of As release in reducing groundwater aquifers     

Kathleen A. Radloff  Anya R. Manning  Brian Mailloux  Yan Zheng  M. Moshiur Rahman  M. Rezaul Huq  Kazi M. Ahmed  Alexander van Geen 《Applied Geochemistry》2008

Microbial Fe reduction is widely believed to be the primary mechanism of As release from aquifer sands in Bangladesh, but alternative explanations have been proposed. Long-term incubation studies using natural aquifer material are one way to address such divergent views. This study addresses two issues related to this approach: (1) the need for suitable abiotic controls and (2) the spatial variability of the composition of aquifer sands. Four sterilization techniques were examined using orange-colored Pleistocene sediment from Bangladesh and artificial groundwater over 8 months. Acetate (10 mM) was added to sacrificial vials before sterilization using either (1) 25 kGy of gamma irradiation, (2) three 1-h autoclave cycles, (3) a single addition of an antibiotic mixture at 1× or (4) 10× the typical dose, and (5) a 10 mM addition of azide. The effectiveness of sterilization was evaluated using two indicators of microbial Fe reduction, changes in diffuse spectral reflectance and leachable Fe(II)/Fe ratios, as well as changes in P-extractable As concentrations in the solid phase. A low dose of antibiotics was ineffective after 70 days, whereas autoclaving significantly altered groundwater composition. Gamma irradiation, a high dose of antibiotics, and azide were effective for the duration of the experiment.  相似文献   

含硫化物脉状矿床成矿流体的中阶段 δD亏损：实例与原因   总被引：2，自引：0，他引：2  

陈衍景  张莉 《地球化学》2008,37(4)

很多含硫化物脉状金银矿床的成矿过程可以大致分为3个阶段,从早到晚分别以形成黄铁矿-石英组合、多金属硫化物和碳酸盐网脉为标志.所谓中阶段δD亏损,是指在成矿流体δ18O逐渐降低(或升高)时,中阶段δD同时低于早阶段和晚阶段的δD.列举了一些矿床的氢氧同位素研究结果,例证了这种现象的存在;根据中阶段伴随大量硫化物沉淀的事实,认为硫化物沉淀时流体中H2S或HS-的H 被金属离子置换出来,H 加入到流体系统后导致了流体的中阶段δD亏损.对不同温度H2O-H2S体系1000In ot值的概算显示,在200-650℃温度范围,H2S或HS-的δD低于H2O的δD约211‰～478%‰,H2S或HS-中H 的少量释放即可导致流体水δD的显著降低.因此建议,成矿流体从早到晚δ18O逐渐降低,中阶段δD亏损的规律,可以作为含硫化物脉状矿床氢氧同位素演化的概念性模型.  相似文献   

针式微萃取结合GC-IRMS测定水溶液中甲酸、乙酸的稳定碳同位素组成     

李心清  黄代宽  章炎麟  江伟  安宁  胡璐  徐刚 《地球化学》2008,37(6)

甲酸和乙酸稳定碳同位素组成（δ^13C）的分析对环境、食品、制药和自然产品等的研究具有重要的应用价值。但目前尚缺乏有效的测定方法。本研究利用最近出现的针式固相微萃取技术（NeedlEX）,以吹扫．捕集方式对水溶液中的有机酸进行了萃取,然后利用气相色谱．同位素比值质谱联用仪（GC—IRMS）对所萃取的有机酸分子进行了占δ^13C的测定。结果显示,质谱计的信号强度与水溶液中有机酸的浓度存在显著的线性相关关系（R^2〉0．99,P〈0．05）,表明Needl EX对水溶液中有机酸具有稳定的萃取能力。在甲酸与乙酸含量分别不低于300μg／mL与200μg／mL的水溶液中,1000mL的吹扫体积可以使两者δ^13C多次分析结果的相对误差分别保持在3％和1％左右,且整个实验流程没有造成可检测的碳同位素分馏作用。低于这两个浓度界线,则分析误差随浓度的降低迅速增加。本研究虽然是针对水溶液中有机酸δ^13C的测定,其萃取方法对其他水溶性挥发和半挥发有机物δ^13C的分析也同样具有应用价值。  相似文献   

An improvement in CARBOLOG technique and its preliminary application to evaluating organic carbon content of source rocks     

LIU Jun-min  PENG Ping-an  HUANG Kai-quan  ZHANG Lin-ye 《地球化学》2008,37(6)

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储量计算与勘探线剖面计算机辅助成图一体化   总被引：1，自引：0，他引：1  

马小刚  李伟忠  吴冲龙  张夏林 《地质与勘探》2008,44(2):73-76

引入关系教据库和GIS自动编图技术,改进传统的垂直断面法储量计算过程,可实现矿山储量计算和勘探线剖面计算机辅助成图的同步和一体化.在共用的矿山地矿信息点源数据库平台基础上.通过设置本地数据库,形成GIS操作时的外挂属性库,用来保存储量计算和机助成图过程中的动态数据.储量计算中的每一步骤中,用户以GIS为操作界面来同步实现对空间图元和外挂属性的操作,这其中对工程样段组合、矿体边界圈连和剖面制图综合等开发了大量自动化辅助功能.储量计算的各步完成后,勘探线剖面图和储量报表即同步生成.这种改进的工作方式实现了垂直断面法全过程的计算机辅助化,将提高这一传统方法的应用效率.  相似文献   

个旧矿区遥感异常信息解译及找矿远景分析   总被引：3，自引：0，他引：3  

张建东  彭省临  杨斌  刘明  王力 《地质与勘探》2008,44(2):87-91

文章以TM多光谱遥感数据为基本信息源,从实际地质情况出发,采用计算机识别和人工判读相结合,对区内的线形、环形构造进行了解译.应用比值 主成分分析的方法对区内热液弱蚀变信息进行了提取.在此基础上,综合利用已知矿床的分布以及遥感构造信息、遥感蚀变晕信息,结合已有的物化探资料,分析出4个找矿远景区.  相似文献   

桃山铀矿田桃山断裂及其保矿作用   总被引：2，自引：0，他引：2  

张万良 《地质论评》2008,54(6):768-774

桃山铀矿田位于江西省中部,断裂构造发育,既有成矿构造,也有保矿构造,其中斜贯桃山矿田的桃山断裂即是一保矿构造,它形成于车免近时期,走向北东,倾向南东,右行正断,并具铰链断层性质,上盘地块掀斜下落,致使上盘成矿壳层向NW和NE倾斜,由于倾末端的侵蚀深度较小,保矿条件较好,加强这些地带的铀矿勘查和评价具有重要意义。  相似文献