略阳煎茶岭铜镍硫化物矿床Re—Os同位素年龄及其地质意义

采用矿石Re-Os同位素方法对陕西省煎茶岭硫化镍矿床矿石进行了成矿年代学研究,获得了878士27 Ma(1σ)的等时线年龄,首次厘定了该矿床成矿时代为新元古代,成岩成矿基本同时.通过对878 Ma硫化镍矿石初始Re-Os同位素体系的γOs计算和Re/Os值分析表明,其yOs和Re/Os值变化范围大,深部条带状矿石的Re/Os值仅为0.05,yOs为-6.70;块状矿石的Re/Os值范围为4.24～24.43,γOs为-15.37～+280.65,说明成矿过程中有壳源物质的混染;两件样品的γOs为负值(-15.37,-6.70),可能指示其超镁铁质岩浆来源于Re亏损地幔.煎茶岭超基性岩体年龄及其镍矿石的Re-Os等时线年龄与扬子克拉通北缘火山岩浆活动时间相对应,它们是扬子克拉通西北缘晋宁期构造岩浆成矿作用的产物.     

中子活化分析在铼—锇法年龄测定中的应用

同位素稀释中子活化分析铼与感耦等离子体质谱法测定锇相结合，应用于辉钼矿及铜＿镍硫化物矿物的铼＿锇年龄测定，取得了满意的结果，扩大了铼＿锇测年法的应用范围。     

四川呷村黑矿型矿床硅质岩的硅、氧同位素组成及其与现代海底硅质烟囱比较研究

本文首次报道了川西呷村黑矿型矿床硅质岩的硅、氧同位素组成,其δ~(18)O为12.8‰-18.3‰纵,形成温度约99-120℃,δ~(30)Si为0.0‰-1.5‰,与Mariana和GalaPagos热液硅质烟囱的δ~(30)Si值范围基本相当,揭示两者具相似的形成机制。硅质岩和硅质烟囱δ~(30)Si最大值与相伴火山岩δ~(30)Si值一致,反映硅质来自被热液淋滤交代的火山岩系。根据SiO_2溶解度-温度关系提出,来自海底之下1-2km处的水-岩反应带、温度高于320℃的初始流体,通过绝热上升或传导冷     

建德铜矿床的海底喷流沉积成因

建德铜矿床是浙江西部多金属成矿带中一个引人瞩目的重要矿床。它产于中石炭统底部伴有火山岩、硅质岩和碧玉岩的白云岩中。整合块状矿体之下有一筒状矿化蚀变带。其成分以Ｃｕ＞Ｚｎ＞Ｐｂ为特征。根据矿床地质、地球化学特征以及近年来研究所获得资料，认为该矿床属海底喷流沉积成因     

内蒙古镁铁质-超镁铁质岩型铜镍矿床成矿条件与找矿远景分析

按构造环境控岩控矿特点,划分区内铜镍型矿成矿(岩)带,分析成矿条件,研究了与该类矿床成矿有关的镁铁质岩、超镁铁质岩分布规律及铜镍硫化物成矿特征,提出了找矿方向和建议.     

石岭沟-拐道沟铜-铅-锌多金属成矿带成矿地质条件分析

成矿带位于北秦岭北部晚元古代-早古生代裂谷带南缘的变质火山岩区，受油房-皇台断裂的次级分支断裂及燕山-印支期的侵入岩体及次火山岩脉的联合控制，成矿地质条件与甘肃白银厂铜-铅-锌矿田相类似，成矿带内地表已发现多条铜-铅-锌矿(化蚀变)体，找矿潜力较大，只要进一步深入开展工作，有望找到与白银厂铜-铅-锌矿田相类似的大型一超大型铜-铅-锌多金属矿床。     

Improved Platinum-Group Element Extraction by NiS Fire Assay from Chromitite Ore Samples Using a Flux Containing Sodium Metaphosphate

Many chromite-rich rocks contain relatively high concentrations of the platinum-group elements (PGE). In many cases, the phases carrying PGE occur as either platinum-group minerals (PGM) or as base metal sulfides in solid solution in sulfides. In some cases, such as the UG-2 unit of the Bushveld Complex, the PGM are occluded inside chromite grains. Chromites are notably difficult to dissolve in most fluxes and if the chromite contains some PGM the possibility exists that not all the PGE will be recovered during fusion. In this work, shortcomings in published methods of analysis based on the nickel sulfide fire assay procedure were investigated and a new procedure developed based on the addition of sodium metaphosphate to the fusion mixture. Optimum composition of the fusion mixture was found to be 10 g sodium metaphosphate and 9 g silica to 10 g sample, 15 g sodium carbonate, 30 g lithium tetraborate, 7.5 g nickel and 4.5 g sulfur to achieve complete dissolution of chromite grains. The new flux mixture was evaluated by the analysis of reference material CHR-Pt+ (which is known to contain PGM inside chromite grains) and no undissolved chromite grains were found in the glassy slag. Analysis of the nickel sulfide beads from this fire assay using neutron activation analysis showed similar results for Rh and Ru when compared with published conventional true (or accepted) values, while Au, Ir, Os, Pd and Pt values determined here were 10 to 30% higher than the corresponding published conventional true values. It was concluded that the addition of sodium metaphosphate improved chromite dissolution in the flux and appears to improve PGE recovery.     

Chemical Composition of Ores from the Takara Volcanogenic Massive Sulfide Deposit, Central Japan

Abstract. The Takara volcanogenic massive sulfide (VMS) deposit occurs in Miocene formation of the Misaka Mountain, the South Fossa Magna region, central Japan. The tectonic setting of the Misaka Mountain is reconstructed to be a part of the paleo Izu-Ogasawara arc which collided with the Honshu arc and to form accreted body in the present position. The Takara deposit, therefore, is considered to have formed in the paleo Izu-Ogasawara arc.
The ores from the Takara deposit are classified into pyrite-type ore, chalcopyrite-type ore, and sphalerite-type ore on the basis of chemical composition and their mineral assemblages. Some pyrite-type ores are characterized by their high Au content. The Au content is hardly recognized in the chalcopyrite-type and sphalerite-type ores.
The ores from the Takara deposit have intermediate bulk chemical composition between those from the Besshi-type deposits and the Kuroko-type deposits that are two representative VMS deposits. However, the bulk chemical composition is closer to that from the Kuroko-type deposits. And moreover, chemical composition of tetrahedrite-tennantite series minerals (tetrahedrite) is similar to that from the Kuroko-type deposits. The bulk chemical composition (Cu, Zn, Co, Pb, and As contents) of ores is affected by the chemical composition of volcanic rocks associated with VMS deposits.     

GEOCHEMICAL CHARACTERISTICS OF PLATINUM GROUP ELEMENTS IN JINCHUAN SUPER-LARGE SULFIDE COPPER-NICKEL DEPOSIT, JINCHANG CITY, GANSU PROVINCE, CHINA

The platinum-group element geochemistry of rocks and ores from Jinchuan super-large copper-nickel sulfide deposit is systemically studied in this paper. The Cu/Pd mean ratio of Jinchuan intrusion is lower than that of original mantle magma, which indicates that these ultrabasic rocks were crystallized from magma that lost Pd in the form of melting segregation of sulfides. The PGE of the rocks show trend of partial melting, similar to that of mantle peridotite, which shows that magma formation occurs during rock-forming and ore-forming processes. The chondrite normalized PGE patterns of the rocks and ores are well related to each other, which signifies the signatures of multi-episode magmatic intrusion, melting and differentiation in the formation processes of rocks and ores. In addition, analyses about the relation between PGE and S, and study on Re-Os isotopes indicate that few contamination of the crustal substances occurred during the magmatic intrusion and the formation of deposit. However, contamination by crustal substances helps to supply part of the S for the enrichment of PGE. Meanwhile, the hydrothermal process is also advantageous for the enrichment of PGE, especially lbr Pt and Pd, due to deep melting segregation. The characteristic parameters （such as Pt/（Pt＋Pd）, （Pt＋Pd）/（Ru＋Ir＋Os）, Pd/Ir, Cu/（Ni＋Cu）, and so on.） for platinum-group elements for Jinchuan sulfide copper-nickel deposit show the same features as those for sulfide copper-nickel deposit related to basic magma, which also illustrates its original magma property representative of Mg-high tholeiite. Therefore, it is the marie （not ultramafic） magma that resulted in the formation of the superlarge sulfide copper-nickel deposit enriched in Cu and PGE. To sum up, the geochemical characteristics of platinum-group elements in rocks and ores from Jinchuan copper-nickel sulfide deposit are constrained by the continental rift tectonic environment, the parent magma features, the enriched mantel magma source, the complex metallogenesis and PGE geochemical signatures, and this would be rather significant for the study about the genetic mechanism of copper-nickel sulfide deposits.     

Lead-arsenic soil geochemical study as an exploration guide over the Killik volcanogenic massive sulfide deposit, Northeastern Turkey

A mountainous terrain, the eastern Pontide tectonic belt, located in northeastern Turkey, contains more than 60 known volcanogenic massive sulfide (VMS) deposits that differ in reserves (0.1–30 million tonnes) and grades. Soil geochemistry is conventionally used in exploration programs to discover concealed VMS deposits in the region. In the present study, Pb and As element pair were used as pathfinder elements to investigate the relationship of their anomalies to a completely delineated ore deposit (Killik VMS deposit) in an orientation survey that served as a natural physical model. Two hundred forty soil samples were analyzed in the present study. The two elements, which represent the opposite ends of the mobility range, revealed high contrast and overlapped each other at the location of the ore deposit due to enhancement of the anomalies by hydromorphic dispersion, which is an indication that soil samples would produce reliable results. The successful delineation of the deposit is remarkable considering the rough topography and the climatic limitations. Previously the extremely moist and temperate climate was thought to cause excessive leaching of the trace element pathfinders from the ore deposits to produce extensive anomalies usually extending away from the mineralization thus, leading to erroneous results and/or extensive anomalous areas. But the present research has shown that the method can be used effectively if the sampling and data evaluation is carefully conducted.