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   

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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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   

冀北万全寺银金矿床地质地球化学特征     

王宝德  牛树银  孙爱群  刘亚明  郭鹏志  孙双海 《地质与勘探》2008,44(1):15-20

万全寺银金矿床位于张宣幔枝构造东侧的侏罗纪断陷盆地中,成矿时限晚于133.33Ma～101.82 Ma.通过硫、铅、氢、氧、碳及稀有气体同位素研究认为,成矿物质应源自地球深部,在中生代冀西北幔枝构造演化过程中集中成矿.成矿热液以岩浆水为主并加入了部分天水.  相似文献   

南海东北部下地壳高速层的成因探讨   总被引：2，自引：0，他引：2  

刘安  武国忠  吴世敏 《地质论评》2008,54(5):609-616

通过对南海北部大陆边缘地壳结构分析,指出南海东北部存在下地壳高速层,大致分布在112°E~120°E,19°N~22°N的陆坡和拉张程度大的陆架地区,呈NEE向延伸,在海底地震仪剖面上最大的厚度有8km,向南海海盆方向减薄。通过对比综合分析认为,高速层物质组成是底侵作用形成的熔岩垫,由于伸展作用,南海海底扩张（30Ma）前后底侵作用形成了熔岩垫,并促使南海北部大陆边缘地壳抬升,导致区域性抬升剥蚀。  相似文献   

云南罗平中三叠世安尼期生物群的发现及其意义   总被引：15，自引：0，他引：15  

张启跃  周长勇  吕涛  谢韬  楼雄英  刘伟  孙媛媛  江新胜 《地质论评》2008,54(4):523-526

本文介绍了云南罗平地区新发现的罗平生物群的产出层位、生物面貌、保存特征、古地理位置及其研究意义。该生物群产于关岭组二段薄层泥晶灰岩中,地层对比和化石鉴定表明其时代为中三叠世安尼期,以鱼类为主,伴生有爬行类、两栖类（？）、棘皮动物、节肢动物（甲壳类、昆虫等）、双壳类、腹足类以及植物化石;化石保存完好,分布广泛,埋藏方式独特。罗平生物群无论在丰度、分异度及化石保存上都极为罕见和独特,对研究埋藏学、古生态学、古地理以及三叠纪海洋生物尤其是海生爬行类都具有极为重要的意义。  相似文献   

邹平王家庄铜矿床成矿地球化学及成因探讨   总被引：2，自引：0，他引：2  

张军  徐兆文  李海勇  刘苏明  杨小男  陆现彩  李红超 《地质论评》2008,54(4):466-476

王家庄铜矿床的矿化脉石英中流体包裹体均一温度介于116 ~ 566 ℃之间,均值为 289 ℃;盐度介于7.2%～63.2% NaCleq,均值为21.1% NaCleq。流体的气相成分主要为H2O和CO2。在均一温度为240 ~ 440 ℃区间内,出现了富气相的两相水溶液包裹体、富液相的两相水溶液包裹体和含子晶的三相水溶液包裹体共存现象,以及加温后富气相包裹体均一到气相和同期富液相包裹体均一到液相的特征,表明成矿流体曾发生过沸腾作用;其中第一次发生于360 ~ 400 ℃,主要形成高温、高盐度含子晶的三相水溶液包裹体和高温、中盐度富液相的两相水溶液包裹体及高温、低盐度富气相的两相水溶液包裹体;第二次发生于240 ~ 320 ℃,主要形成高—中温、高盐度的含子晶的三相水溶液包裹体和高—中温、中盐度富液相的两相水溶液包裹体及高—中温、低盐度富气相的两相水溶液包裹体;之后主要形成富液相的两相水溶液包裹体,具有中低温和中盐度的特征。矿化脉石英中的δ18OH2O介于-1.14‰ ~ 1.79‰之间,均值为0.94‰;δD介于-63.70‰ ~ -56.50‰之间,均值为-59.8‰;说明王家庄铜矿床的成矿流体主要来源于岩浆,后期混入大气降水。矿石矿物的δ34S变化于-8.80‰ ~ -2.80‰之间,均值为-6.33‰。矿石矿物的n(206Pb)/n(204Pb)介于18.1684 ~ 18.3637之间,均值为18.2892;n(207Pb)/n(204Pb)介于155546 ~ 156342之间,均值为155777;n(208Pb)/n(204Pb)介于38.1286 ~ 38.4840之间,均值为38.2780。说明矿石具有贫重硫和富放射性成因铅的特征,硫、铅主要来源于深部,后期可能受到地壳物质或大气降水的混染。  相似文献