Age and depositional environment of the Draa Sfar massive sulfide deposit, Morocco

The Draa Sfar mineralization consists of two main stratabound orebodies, Sidi M’Barek and Tazacourt, located north and south of the Tensift River (“Oued Tessift”), respectively. Each orebody is comprised by at least two massive sulfide lenses. The hosting rocks are predominantly black shales, although minor rhyolitic rocks are also present in the footwall to the southern orebody. Shales, rhyolitic volcanic rocks, and massive sulfides are all included into the Sarhlef Series, which is recognized as one of the main stratigraphic units of the Moroccan Variscan Meseta. Hydrothermal activity related with an anomalous thermal gradient, together with a high sedimentation rate in a tectonically driven pull-apart marine basin, favored the accumulation of organic-rich mud in the deepest parts of the basin and the sedimentary environment suitable for massive sulfide deposition and preservation. This took place by replacement of the hosting unlithified wet mud below the sediment–water interface. Geochemical data suggest a sedimentary environment characterized by oxic water column and anoxic sediment pile with the redox boundary below the sediment–water interface. The low oxygen availability within the sediment pile inhibited oxidation and pyritization of pyrrhotite. Biostratigraphic analysis, based on the palynological content of the hosting black shales, restricts the age of the sulfides to the Asbian substage (mid-Mississippian). This age is consistent with earlier geochronological constraints.     

Anhydrite pseudomorphs and the origin of stratiform Cu–Co ores in the Katangan Copperbelt (Democratic Republic of Congo)

The stratiform Cu–Co ore mineralisation in the Katangan Copperbelt consists of dispersed sulphides and sulphides in nodules and lenses, which are often pseudomorphs after evaporites. Two types of pseudomorphs can be distinguished in the nodules and lenses. In type 1 examples, dolomite precipitated first and was subsequently replaced by Cu–Co sulphides and authigenic quartz, whereas in type 2 examples, authigenic quartz and Cu–Co sulphides precipitated prior to dolomite and are coarse-grained. The sulphur isotopic composition of the copper–cobalt sulphides in the type 1 pseudomorphs is between −10.3 and 3.1‰ relative to the Vienna Canyon Diablo Troilite, indicating that the sulphide component was derived from bacterial sulphate reduction (BSR). The generation of during this process caused the precipitation and replacement of anhydrite by dolomite. A second product of BSR is the generation of H₂S, resulting in the precipitation of Cu–Co sulphides from the mineralising fluids. Initial sulphide precipitation occurred along the rim of the pseudomorphs and continued towards the core. Precipitation of authigenic quartz was most likely induced by a pH decrease during sulphide precipitation. Fluid inclusion data from quartz indicate the presence of a high-salinity (8–18 eq. wt.% NaCl) fluid, possibly derived from evaporated seawater which migrated through the deep subsurface. ⁸⁷Sr/⁸⁶Sr ratios of dolomite in type 1 nodules range between 0.71012 and 0.73576, significantly more radiogenic than the strontium isotopic composition of Neoproterozoic marine carbonates (⁸⁷Sr/⁸⁶Sr = 0.7056–0.7087). This suggests intense interaction with siliciclastic sedimentary rocks and/or the granitic basement. The low carbon isotopic composition of the dolomite in the pseudomorphs (−7.02 and −9.93‰ relative to the Vienna Pee Dee Belemnite, V-PDB) compared to the host rock dolomite (−4.90 and +1.31‰ V-PDB) resulted from the oxidation of organic matter during BSR.     

Mineralogy and composition of Kuroko deposits from northeastern Honshu and their possible modern analogues from the Izu-Ogasawara (Bonin) Arc south of Japan: Implications for mode of formation

The Kuroko deposits of NE Honshu are a key type deposit for the study of volcanogenic massive sulfide deposits. However, these deposits have not been studied in detail since the early 1980's and knowledge of their mode of formation is now dated. In this study, we present the analysis of 12 samples of the Kuroko deposits, 12 samples of submarine hydrothermal minerals from the Sunrise deposit and 6 samples from Suiyo Seamount, both of which are located on the Izu-Ogasawara (Bonin) Arc, for 27 elements. For the Kuroko deposit, Cd>Sb>Ag>Pb>Hg>As>Zn>Cu are highly enriched, Au>Te>Bi>Ba>Mo are moderately enriched, In>Tl are somewhat enriched and Fe is not significantly enriched relative to the average continental crust. Within each of these deposits, a similar pattern of element associations is apparent: Zn–Pb with As, Sb, Cd, Ag, Hg, Tl and Au; Fe–Cu–Ba with As, Sb, Ag, Tl, Mo, Te and Au; Si–Ba with Ag and Au; CaSO₄. The enrichment of the chalcophilic elements in these deposits is consistent with hydrothermal leaching of these elements from the host rocks which are dominantly rhyolite–dacite in the case of the Kuroko deposits, rhyolite in the case of the Sunrise deposit and dacite–rhyolite in the case of the Suiyo Seamount deposit. However, this pattern of element enrichment is also similar to that observed in fumarolic gas condensates from andesitic volcanoes. This suggests that there may be a significant magmatic contribution to the composition of the hydrothermal fluids responsible for the formation of the Kuroko deposits, although it is not yet possible to quantify the relative contributions of these two sources of elements.The compositional data show that Sunrise and Suiyo Seamount deposits are much closer compositionally to the Kuroko deposits from NE Honshu than are the submarine hydrothermal deposits from the JADE site in the Okinawa Trough which contain, on average, significantly higher concentrations of Pb, Zn, Sb, As and Ag than each of these deposits. In spite of the greater similarity in tectonic setting of the Hokuroku Basin in which the Kuroko deposits formed to the Okinawa Trough (intracontinental rifted back-arc basin) compared to Myojin Knoll and Suiyo Seamount (active arc volcanoes), it appears that submarine hydrothermal deposits from Myojin Knoll and Suiyo Seamount are closer analogues of the Kuroko deposit than are those from the Okinawa Trough. The present data are consistent with the magmatic hydrothermal model for the formation of Kuroko-type deposits as formulated by Urabe and Marumo [Urabe, T., Marumo, K., 1991. A new model for Kuroko-type deposits of Japan. Episodes 14, 246–251].     

火试金法测定铜精矿中金含量结果的不确定度评定

对火试金法测定铜精矿中金含量的结果进行不确定度评定。分析了铜精矿样品称量、铜精矿样品的不均匀性和配料处理,以及金粒称量等因素对金含量测量结果不确定度的影响,并得出火试金法测量铜精矿中金含量的扩展不确定度。     

河南省栾川县罗村钼矿成矿特征及找矿

通过对河南省栾川县罗村钼矿区域地质背景、矿床地质特征与南泥湖、三道庄及东沟超大型钼矿的综合对比、分析、研究,总结归纳了矿区NWW构造形迹、小岩体与钼矿成矿关系、围岩对成矿的控制作用、围岩蚀变与成矿的关系、地球化学异常与钼矿床的关系等成矿特征.根据罗村钼矿的成矿特征,初步指出今后的找矿方向.     

河南洛宁段河金矿流体包裹体研究和矿床成因

河南省洛宁县段河石英脉型金矿主要包括石寨沟和岭东两个矿区,分别由3～4条含金石英脉构成。矿化过程从早到晚包括石英-黄铁矿、石英-多金属硫化物和石英-碳酸盐等3个阶段．其中中阶段金矿化最强,次为早阶段。各阶段石英中流体包裹体以气液两相包裹体为主．次为纯液体包裹体。激光拉曼测试表明,气液两相包裹体的液相为H2O,气相主要为Ho和CO2混合、纯H2O,次为纯CO2;纯液体包裹体为纯H2O。石寨沟矿区包裹体均一温度从早到晚依次为240．9～315．9℃．188．7～304．5℃,137．3～259．3℃：流体盐度变化依次为（6．74～12．85）wt%NaCl．eq,（2．41～8．68）wt％NaCl．eq,（2．24-7．86）wt%NaCl．eq。岭东矿区均一温度从早到晚依次为303．7-343．1℃,251．8-325．4℃,305．7～355．0℃：流体盐度变化依次为（5．11～11．70）wt％NaCl．eq,（2．74-10．11）wt％NaCl．eq,（0．53-6．74）wt％NaCl．eq。两矿区主成矿期流体均为中温、低盐度,早阶段流体为改造热液和变质热液的混合体,含一定量CO2,且流体CO2含量和盐度从早到晚逐渐降低。石寨沟矿区包裹体均一温度逐渐降低,而岭东矿区包裹体均一温度先降后升,加之岭东矿区各阶段成矿温度均高于石寨沟矿区．表明成矿流体系统主要受岩浆热驱动,岭东矿区更靠近岩体,且在晚阶段又有脉动性的岩浆加热．段河金矿区南部存在隐伏岩体。     

安徽铜陵朝山金矿床流体包裹体研究

朝山金矿床是狮子山矿田内的热液交代型金矿床,在成因上与燕山期的白芒山辉石闪长岩有关.通过采集发育在不同深度下的含金黄铁矿-石英一方解石脉样品,进行流体包裹体岩相学观察和显微测温发现,石英和方解石中均捕获了富气相、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,以上三种类型包裹体的均一温度统计峰值分别出现于315～335℃和255～275℃,盐度的统计峰值出现于17.50%～22.50%NaCl eq.和32.50%～37.50%NaCl eq.之间.激光拉曼探针分析表明,石英中流体包裹体的气相成分以水蒸汽为主,伴有少量CO2,可能含有CH4.流体的H、O同位素组成具确岩浆水特征.上述研究表明.朝山金矿成矿流体经历了相态变化,发生了不均匀捕获.受燕山期岩浆作用影响,狮子山矿田内的铜、金成矿在时空上具有一定联系,成矿流体运移的过程中,主要发生了相分离、气相液化和减压沸腾作用,可能是形威铜、金矿化分带的重要原因.     

胶东三甲金矿床流体包裹体特征

三甲金矿是胶东牟平-乳山金成矿带内重要的石英脉型金矿,金主要产于黄铁矿和多金属硫化物石英脉中。流体包裹体研究表明,三甲金矿蚀变岩石和各成矿阶段金矿石中的流体包裹体主要有三种类型：H2O-CO2包裹体、富CO2包裹体和H2O溶液包裹体。早期乳白色石英中主要赋存原生的H2O-CO2包裹体;成矿期黄铁矿石英脉和多金属硫化物石英脉中的富CO2包裹体主要为原生,随机分布,气液比变化较大,常与早期H2O溶液包裹体共生且均一温度接近,显示不混溶流体包裹体组合特征;在成矿晚期的石英和方解石中主要发育原生H2O溶液包裹体。显微测温结果显示,成矿前（第1阶段）H2O-CO2包裹体的完全均一温度（Tb．TOT,至液相）为280℃至416℃,成矿期（第Ⅱ和Ⅲ阶段）富CO2包裹体的完全均一温度为210—330℃,同期的H2O溶液包裹体均一温度为253～377℃,成矿后（第Ⅳ阶段）H2O溶液包裹体的均一温度为176—207℃。成矿流体为低盐度的CO2-H2O-NaCl型热液,成矿应力场转变导致的流体减压沸腾作用可能是三甲金矿金沉淀成矿的主要原因。     

岩矿显微组构对水银洞金矿成因的指示

黔西南水银洞金矿为产于上二叠统龙潭组中的超大型、高品位金矿床,矿床由多个金矿体组成.工业金矿体顺层产于龙潭组含煤地层所夹的玄武质、硅质、生物碎屑碳酸盐岩中.对水银洞金矿赋矿地层岩石以及矿石显微组构进行了研究,矿石中主要载金矿物为细粒黄铁矿,具再生边、粒内孔隙、铸模孔隙结构及镶边生物矿化构造、铸模式生物矿化构造,是一典型的具沉积一成岩组构.金矿化与硅化有密切的成因联系,金与SiO2来源于峨嵋山玄武岩的喷溢活动,主要金矿体更多显示与峨嵋山玄武岩准同生特征.矿床为沉积一成岩弱改造成囚金矿床.     

南极冰退与深圳湾北岸海平面变化的地质记录

南极冰层的冰量为２４．５×１０６ｋｍ３，占地球总冰量的９０％以上，南极冰川进退控制着全球海平面变化和气候波动。酉部南极乔治王岛第四纪冰碛与湖积剖面记录了近１２０００ａ来南极曾于距今１１０００ａ，９０００ａ和６１００ａ出现过３次快速的冰消过程，近６０００ａ来是一小幅度冷暖交替的气候波动过程。深圳湾北岸潮间带堆积是在近６０００ａ以来发育的，堆积物的环境记录表明，海平面呈周期性升降变化，波动周期平均为６７０ａ，低海面时期发生于距今５５００—４９００ａ，３９００—３６００ａ，２４００—２２００ａ和１３００—１２００ａ。相邻低海面间则是海面上升时期，每一升降周期的海平面变化幅度为８０ｃｍ左右，近１００ａ的现代增温，海平面处于上升阶段，上升速率为２—３ｍｍ·ａ（－１）。