云南宁蒗地区喜山期斑岩带岩石化学特征和岩浆来源与成矿     

徐旃章  张寿庭 《矿物岩石》1995,15(4):20-29

宁蒗地区喜山期斑岩带为扬子西缘构造活动带喜山期构造－斑岩成矿带的重要组成部分，通过斑岩体岩石化学特征等的综合分析研究，得出了岩浆物质源于幔源，并有陆壳组分参与的壳幔混源型岩浆，斑岩体属含铜斑岩或铜斑岩。斑岩带具良好的成矿地质条件与前景。  相似文献   

载金石英的阳离子效应及其对含矿性的指示意义   总被引：2，自引：0，他引：2  

颜文  傅平秋 《矿产与地质》1993,7(4):273-277

石英的阳离子效应指石英结构中Al~(3+)与Si~(4+)的置换作用.在分析海南戈枕断裂金成矿带石英中普遍存在的这一作用,以及由此造成的石英粉末红外谱(IR)、顺磁共振谱(EPR)及热释光曲线(TL)特征,进而讨论了这些特征与金成矿的关系.  相似文献   

八卦庙金矿床石英脉的控矿作用初探   总被引：3，自引：0，他引：3  

韦龙明  王建业 《矿产与地质》1993,7(5):329-333

八卦庙金矿床的矿石品位与其石英脉发育程度和破碎程度、共生硫化物的含量成正比,与脉体的厚度、共生硫化物的粒度成反比;节理脉的含金量比顺层脉的含金量高;石英细脉的含金量高于脉旁围岩的含金量数倍至十多倍,但含金石英脉不能单独构成工业矿体.据此,作者首次提出金矿化类型属于细脉浸染型金矿,揉皱石英细(网)脉破碎带是此类金矿的一种重要而直观的找矿标志.  相似文献   

大春河—一朵云断裂断层泥中石英表面 SEM 特征的分析研究   总被引：1，自引：0，他引：1  

俞维贤  杨继武  吴伯黔 《地震研究》1993,(1)

大春河—一朵云断裂位于昆明市的东南侧,沿断层线断错水系、土林地貌发育,河流的最大左旋扭动距离达两公里。断层泥中石英碎砾的SEM研究表明:断层的强烈活动时期为早更新世晚期和晚更新世,全新世断层的活动有所减弱;晚更新世以来断裂的活动方式以蠕滑为主。  相似文献   

阳原盆地化稍营地区断层主要活动时期的研究     

唐汉军  刘行松 《华北地震科学》1993,11(2):35-44

研究一个地区断层主要活动时期是了解地壳构造运动或断层发育历史的基础。本文仍沿用了传统研究法,并将同位素法和石英形貌法测年与显微构造分析法引进到研究断层主要活动时期的工作中,取得了能相互映正的结果,最后确定阳原盆地化稍营地区的断层经历过:元古代前;燕山期;6～9千万年;上新世——早更新世和最后一次较强烈活动在20—30万年以前等五次主要活动时期。  相似文献   

甘肃公婆泉铜矿区斑岩岩浆起源及成岩成矿大地构造背景   总被引：9，自引：0，他引：9  

游小毛 《大地构造与成矿学》1999,23(2):167-171

探讨了公婆泉矿区斑岩岩浆起源,论述了该矿区斑岩成岩成矿大地构造背景。研究结果表明,该矿区斑岩岩浆起源属幔壳混合源;斑岩成岩成矿大地构造背景为褶皱造山期。  相似文献   

我国浅成热液金矿的分类探讨   总被引：1，自引：0，他引：1  

刘连登  陈国华  吴国学  张克尧  石建基  张进高 《吉林大学学报(地球科学版)》1999,29(3):222-226

陆相浅成热液金矿是个大概念,是数类金矿的统称。目前对其的分类,不适应理论和应用研究的需要。本文主张以成矿地球动力学环境和矿床本质特征为准则,实施浅成热液金矿的分类。对类型的划分努力体现成因类型和工业类型相结合的原则,并充分反映我国的特点。在矿床类型具体命名时,突出成矿时的浅成深度。文中将我国浅成热液金矿分为浅成脉型、浅成斑岩型和浅成矽卡岩型等三大类八个亚类。陆相浅成热液金矿在我国有广阔的找矿前景,而且在地质产状和成矿作用等方面与国外的殊为不同,值得对其作深入的理论与应用研究。  相似文献   

Adakite-like signature of Late Miocene intrusions at the Los Pelambres giant porphyry copper deposit in the Andes of central Chile: metallogenic implications   总被引：7，自引：0，他引：7  

Martin?Reich  Miguel?A.?ParadaEmail author  Carlos?Palacios  Andreas?Dietrich  Frank?Schultz  Bernd?Lehmann 《Mineralium Deposita》2003,38(7):876-885

Adakite-like features are recognized in the Late Miocene (~10 Ma) porphyritic intrusions of the Los Pelambres giant porphyry copper deposit, central Chile (32°S). Located within the southern portion of the flat-slab segment (28–33°S) of the Chilean Andes, the Al- and Na-rich porphyries of Los Pelambres display distinctly higher Sr/Y (~100–300) and La_N/Yb_N (~25–60) ratios than contemporaneous and barren magmatic units (e.g., La Gloria pluton, Cerro Aconcagua volcanic rocks) of the same Andean magmatic belt. Strong fractionation of heavy rare earth elements (HREE), absence of Eu anomalies, high Sr/Y and Zr/Sm and low Nb/Ta ratios suggest melt extraction from a garnet-amphibolite source. The Late-Miocene adakite-like porphyritic intrusions at Los Pelambres formed closely related in time and space to the subduction of the Juan Fernández Ridge (JFR) hotspot chain along the Chilean margin. Current tectonic reconstructions reveal that, at the time of formation of the Los Pelambres rocks, a W-E segment of the JFR started to subduct beneath them, producing a slow-down of a previously rapid southward migration of a NE-ridge—trench collision. These particular tectonic conditions are favorable for the origin of the Los Pelambres porphyry suite by melting of subducting young hotspot rocks under flat-slab conditions. The incorporation of crustal components into the oceanic lithopheric magma source by subduction erosion is evidenced by the Sr-Nd isotope composition of the Los Pelambres rocks different from the MORB signatures of true adakites. A close relationship apparently exists between the origin of this adakite-like magmatism and the source of the mineralization in the Los Pelambres porphyry copper deposit.Editorial handling: R.J. Goldfarb  相似文献   

Analyses of trace elements on quartz surfaces in sulfidic mine tailings from Kristineberg (Sweden) a few years after remediation     

B.?MüllerEmail author  M.?D.?Axelsson  B.??hlander 《Environmental Geology》2003,45(1):98-105

Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) has been applied to determine the elemental composition of the surface layer, as well as of the first interior layer, of quartz grains from the mine tailings from Kristineberg (northern Sweden) in order to determine concentration gradients between these two layers. The quartz grains were collected from the oxidized and unoxidized zones within the tailings. The aim of this study is to assess the role of quartz surfaces as sites for the attenuation of solutes from the mine-tailings porewater. Concentrations of Cu, Ag, Sb, Pb and Bi are highest near the surface of each grain and decrease towards the interior. The surface concentration of Cu, Zn and Pb is more pronounced within the unoxidized than within the oxidized zone of the tailings. Cu exhibits a distinct concentration peak at the surface of the quartz grains below the pre-remediation oxidation front. For Zn and Ce the trend of high surface concentration is less pronounced than for Cu or Pb. Silver, Bi and As are preferably adsorbed within the uppermost layers of the oxidized zone where the pH is as high as 6.2. The conversion of intensity signals of the elements to concentration values in ppm was done by using external standards (NIST silicate glass).  相似文献   

A mapping of the electron localization function for the silica polymorphs: evidence for domains of electron pairs and sites of potential electrophilic attack     

G. V. Gibbs  D. F. Cox  T. D. Crawford  M. B. Boisen Jr  M. Lim 《Physics and Chemistry of Minerals》2002,29(5):307-318

The electron localization function, η, evaluated for first-principles geometry optimized model structures generated for quartz and coesite, reveals that the oxide anions are coordinated by two hemispherically shaped η-isosurfaces located along each of the SiO bond vectors comprising the SiOSi angles. With one exception, they are also coordinated by larger banana-shaped isosurfaces oriented perpendicular to the plane centered in the vicinity of the apex of each angle. The hemispherical isosurfaces, ascribed to domains of localized bond-pair electrons, are centered ～0.70 Å along the bond vectors from the oxide anions and the banana-shaped isosurfaces, ascribed to domains of localized nonbonding lone-pair electrons, are centered ～0.60 Å from the apex of the angle. The oxide anion comprising the straight SiOSi angle in coesite is the one exception in that the banana-shaped isosurface is missing; however, it is coordinated by two hemispherically shaped isosurfaces that lie along the bond vectors. In the case of a first-principles model structure generated for stishovite, the oxide anion is coordinated by five hemispherically shaped η-isosurfaces, one located along each of the three SiO bond vectors (ascribed to domains of bonding-electron pairs) that are linked to the anion with the remaining two (ascribed to domains of nonbonding-electron pairs) located on opposite sides of the plane defined by three vectors, each isosurface at a distance of ～0.5 Å from the anion. The distribution of the five isosurfaces is in a one-to-one correspondence with the distribution of the maxima displayed by experimental Δρ and theoretical ??²ρ maps. Isosurface η maps calculated for quartz and the (HO) ₃ SiOSi(OH) ₃ molecule also exhibit maxima that correspond with the (3,?3) maxima displayed by distributions of ??²ρ. Deformation maps observed for the SiOSi bridges for the silica polymorphs and a number of silicates are similar to that calculated for the molecule but, for the majority, the maxima ascribed to lone-pair features are absent. The domains of localized nonbonding-electron pair coordinating the oxide anions of quartz and coesite provide a basis for explaining the flexibility and the wide range of the SiOSi angles exhibited by the silica polymorphs with four-coordinate Si. They also provide a basis for explaining why the SiO bond length in coesite decreases with increasing angle. As found in studies of the interactions of solute molecules with a solvent, a mapping of η-isosurfaces for geometry-optimized silicates is expected to become a powerful tool for deducing potential sites of electrophilic attack and reactivity for Earth materials. The positions of the features ascribed to the lone pairs in coesite correspond with the positions of the H atoms recently reported for an H-doped coesite crystal.  相似文献