秦岭造山带的印支运动及印支期成矿作用   总被引：27，自引：10，他引：17  

卢欣祥  李明立  王卫  于在平  时永志 《矿床地质》2008,27(6):762-773

秦岭碰撞造山经历了长期的板块构造的俯冲-碰撞的构造演化,于印支期最终完成对接拼合,形成了统一的中国大陆,并由此转入陆内变形。众多Au、Mo多金属矿床的同位素年龄资料表明,印支期是秦岭的重要成矿期,其成矿作用明显受到构造演化的控制,反映特定的地球动力学背景和作用过程。秦岭印支期成矿作用不仅是中国东部中生代成矿作用的先导和开始,奠定了中国东部中生代成矿大爆发的基础,而且为碰撞期和碰撞期后构造体制快速转换的研究提供了依据。重视秦岭以及中国印支期成矿作用的研究,对正确认识秦岭成矿带的区域成矿规律、造山带演化的深部动力学过程,建立符合中国和东亚实际的印支期成矿理论体系具有重要科学意义。  相似文献   

安徽铜陵狮子山矿田岩浆岩锆石SHRIMP定年及其成因意义   总被引：36，自引：4，他引：32  

徐晓春  陆三明  谢巧勤  柏林  储国正 《地质学报》2008,82(4):500-509

铜陵狮子山矿田发育大量岩浆岩,且与矿田中的铜金多金属成矿关系密切。锆石SHRIMP同位素精确定年表明,矿田中的岩浆侵位年龄在132.4～142.9Ma之间,即晚侏罗世—早白垩世,属燕山早期晚阶段。矿田岩浆岩体是在同期岩浆活动中多次侵位形成的,岩浆侵入活动可以划分为分别起始于140Ma前后和约136Ma的早晚两次。从岩浆上升侵位到冷却结晶的时间间隔均较短,但其中白芒山辉石二长闪长岩冷却史相对较长,且经历了早期深部岩浆房中的分离结晶作用和后期构造脉动、岩浆上升侵位、减压受热、早期晶体再熔蚀及冷却结晶的过程。结合主量元素和微量元素地球化学研究认为,狮子山矿田岩浆演化的后期,即起源于上地幔或下地壳的原生岩浆在同化了壳源物质并聚集到岩浆房中以后,在滞留的过程中发生了一定程度的分离结晶作用,但尚未固结,成分上显示了一定的带状分布,在区域构造应力松弛及构造事件诱发下,随机地沿发育的构造裂隙先后上升侵位,冷凝结晶。  相似文献   

柴达木盆地北缘侏罗系不同沉积环境烃源岩生物标志物特征及其应用   总被引：2，自引：0，他引：2  

曹剑  边立曾  胡凯  刘云田  汪立群  杨少勇  陈琰 《地质学报》2008,82(8):1121-1128

柴达木盆地北缘地区侏罗系(中下侏罗统)的优质烃源岩主要发育于湖相与三角洲相环境。研究了不同时代、不同沉积环境中烃源岩的生物标志物组成特征,结果发现,有3类化合物的分布与组成差异显著,包括三环萜烷(C19、C20、C21)的分布型式、重排藿烷的丰度以及规则甾烷的相对组成。其中,不同时代的差异主要体现在规则甾烷组成上;而不同沉积环境的差异主要体现为三环萜烷(C19、C20、C21)的分布型式及重排藿烷的丰度。分析认为,这些差异与烃源岩的沉积环境及其生源组成有密切关系。据此,初步将这些参数应用于两方面研究,一是为划分地层沉积环境提供“生物标志物相标志”,二是研究油源对比,取得良好效果。因此,本文研究结果具有重要实用价值与参考意义。  相似文献   

力马河镍矿Re-Os同位素研究   总被引：10，自引：0，他引：10  

陶琰 《地质学报》2008,82(9):1292-1304

四川力马河镍矿是峨眉山大火成岩省一个重要的岩浆硫化物矿床。本文通过对其主要岩、矿石类型Re、Os及其同位素组成的分析,综合探讨了成矿岩体原始岩浆性质、矿石硫化物成因、成矿机制及Re-Os同位素等时线年龄。结果表明,力马河镍矿不同类型岩矿石样品初始Os同位素组成是不均一的,富硫化物的网脉状矿石及其选纯硫化物Os同位素组成初值差异较小,其等时线年龄为265±35 Ma、与岩体锆石SHRIMP年龄263±3 Ma基本相当;硫化物含量较低的岩、矿石样品间初始Os同位素组成差异较大,其表观等时线年龄大于成矿年龄。分析认为,岩矿样品初始Os同位素组成的不均一是由含较高放射成因187Os丰度的硫化物熔体和含较低放射成因187Os丰度的硅酸盐熔体不同比例混合造成的。混合模型分析表明,硫化物含量超过30％的矿石样品初始187Os/188Os基本接近,硫化物含量低于30％的岩矿石样品初始187Os/188Os随硫化物含量上的不同差异很大,为岩浆硫化物矿床Re-Os等时线年龄可能出现多组年龄解的现象提供了一种可能的解释。成矿岩体中含放射成因187Os丰度最低的岩石样品γOs（t=260Ma）在5左右、Cu/Pd比值在7000左右,表明是基本没有受到地壳混染及硫化物熔离影响的原始岩浆结晶分异产物,估计原始岩浆Os含量在1×10－9左右,为苦橄质岩浆。矿石硫化物Re/Os比值显著高于任何赋矿橄榄岩,γOs（t=260Ma）高达110左右,综合分析揭示了力马河镍矿硫化物为二次熔离成因,模式分析认为,矿石硫化物是由原始岩浆经历R=2000左右的硫化物熔离后、其亏损岩浆再经R=200左右的硫化物熔离形成,与二次熔离相对应,成矿岩浆也经历了两次混染作用,分别为上、下地壳7％左右的混染。  相似文献   

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   

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   

金川镍铜矿床数学模型对深部矿化变化趋势的指示     

田毓龙  把多恒  高志武  洪托  陈兴义  卢耀军 《地质与勘探》2008,44(1):82-88

按矿化特征将金川X矿区主矿体分为致密块状特富矿、海绵状富矿和浸染状贫矿.应用MicroMine软件对3类矿化体分别建立了数学模型,并应用距离平方反比法对模型单元块进行了镍、铜品位估值.通过分析和对比矿床数学模型900m至1300m不同水平剖面上的Ni、Cu品位及Ni/Cu比值的变化,得出在X矿区的中部西侧是一个Ni和Cu的矿化中心,并且向深部Cu的矿化强度高于Ni.  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   

西藏马攸木金矿床金银互化物的赋存状态   总被引：3，自引：0，他引：3  

孙燕  温春齐  多吉  霍艳 《地质与勘探》2008,44(5):42-46

马攸木金矿床是西藏近年发现的首例规模较大、矿石品位富、金成色高的岩金矿床.作者通过对马攸木金矿床矿石组构、矿石共生组合及矿物特征研究发现,金银互化物主要有自然金、含银自然金、银金矿、自然银.载金矿物为黝铜矿、针铁矿、脆硫锑铅矿及石英;金银互化物的赋存形式主要为包裹体金、裂隙金及粒间金.金银互化物的形成、富集与热液成矿作用及表生风化作用关系密切.  相似文献