The Mordor Alkaline Igneous Complex,Central Australia: PGE-enriched disseminated sulfide layers in cumulates from a lamprophyric magma     

Stephen J. Barnes  J. A. C. Anderson  T. R. Smith  L. Bagas 《Mineralium Deposita》2008,43(6):641-662

The Mordor Alkaline Igneous Complex (MAIC) is a composite intrusion comprising a body of syenite and a funnel-shaped layered mafic–ultramafic intrusion of lamprophyric parentage, the Mordor Mafic–Ultramafic Intrusion or MMUI. The MMUI is highly unusual among intrusions of lamprophyric or potassic parentage in containing primary magmatic platinum-group element (PGE)-enriched sulfides. The MMUI sequence consists largely of phlogopite-rich pyroxenitic cumulates, with an inward dipping conformable layer of olivine-bearing cumulates divisible into a number of cyclic units. Stratiform-disseminated sulfide accumulations are of two types: disseminated layers at the base of cyclic units, with relatively high PGE tenors; and patchy PGE-poor disseminations within magnetite-bearing upper parts of cyclic units. Sulfide-enriched layers at cycle bases contain anomalous platinum group element contents with grades up to 1.5 g/t Pt+Pd+Au over 1-m intervals, returning to background values of low parts per billion (ppb) on a meter scale. They correspond to reversals in normal fractionation trends and are interpreted as the result of new magma influxes into a continuously replenished magma chamber. Basal layers have decoupled Cu and PGE peaks reflecting increasing PGE tenors up-section, due to increasing R factors during the replenishment episode, or progressive mixing of between resident PGE-poor magma and more PGE-enriched replenishing magma. The presence of PGE enriched sulfides in cumulates from a lamprophyric magma implies that low-degree partial melts do not necessarily leave sulfides and PGEs in the mantle restite during partial melting. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

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

C. Moreno  R. Sáez  F. González  G. Almodóvar  M. Toscano  G. Playford  A. Alansari  S. Rziki  A. Bajddi 《Mineralium Deposita》2008,43(8):891-911

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.  相似文献   

Brine-pool deposition for the Zn–Pb–Cu massive sulphide deposits of the Bathurst mining camp, New Brunswick, Canada. II. Ocean anoxia during mineralisation     

Mike Solomon   《Ore Geology Reviews》2008,33(3-4):352-360

Current models of massive sulphide ore genesis in the Bathurst mining camp, New Brunswick, involve settling of sulphide particles from a stagnating, low-salinity hydrothermal plume spreading laterally in an anoxic ocean layer with minimal sulphate content. There is fragmentary evidence of ocean anoxia in the form of local fine lamination in the shales that host some of the deposits but the total organic carbon, S, Fe, U/Th, Ni/Co, V/Ni and V/Cr relationships indicate deposition under oxic or dysoxic conditions. Vanadium and Mn values range from oxic to anoxic and sulphate-reducing to non-sulphate reducing but Mn may be anomalously low due to derivation by erosion of acidic volcanic rocks. The somewhat equivocal physical and chemical data, combined with the likely disturbing effects of penecontemporaneous volcanism, considerably weaken the case for an anoxic bottom layer in a static ocean. The presence of barite with ambient seawater ³⁴S values in Brunswick no. 12 ore, and the abundance of sulphate in modern euxinic basin waters, make a sulphate-free layer unlikely, even if anoxic. Sulphate-bearing, low-salinity fluids mixing with seawater would lead to growth of barite-bearing chimneys and baritic rubble mounds, which are not observed. A model involving brine-pool deposition better explains the major features of the Bathurst ores.  相似文献   

Multivariate analysis of heavy metal contents of sediments from Gumusler creek, Nigde, Turkey   总被引：2，自引：0，他引：2  

M. Gurhan Yalcin  Ibrahim Narin  Mustafa Soylak 《Environmental Geology》2008,54(6):1155-1163

In this study, heavy metal contents of samples from Gumusler creek in Turkey were studied and the metal contamination characteristics were investigated. In this respect, considering the pollutant sites in the area, systematic sediment samples were collected in a zone starting from the manifestation part of the water to the entrance of the Karasu creek in Gumusler town. Samples were taken from lower section of the river bed at 30 stations along Gumusler creek, 13 km in length and their heavy metal contents were analyzed with XRF Spectrometer. Correlation coefficients, element coefitic coefficient correlation, dendogram hierarchical cluster, model summary and Annova analysis statistical methods were applied to data. Strong positive correlations were determined for some elements which are believed to have possibly the same origin. In addition, mineralizations in the area are thought to cause variation in metal contents. Results of chemical analysis show that soil limit values and clark values were exceeded. The heavy metal accumulation in the creek is believed to be derived from non-operated Sb-Hg-W and Fe quarries.  相似文献   

Trace metals in suspended particulate matter and in sediment trap material from a permanently anoxic fjord — Framvaren, South Norway     

Jens M. Skei  Douglas H. Loring  Reijo T. T. Rantala 《Aquatic Geochemistry》1996,2(2):131-147

Geochemical studies of the trace metal concentrations in suspended particulate matter (SPM) and sediment trap material from a permanently anoxic fjord, Framvaren, South Norway in 1989 and 1993 indicate that extremely high concentrations of zinc (max = 183920 mg/kg), copper (max = 4130 mg/kg), lead (max = 2752 mg/kg), and cadmium (max= 8.1 mg/kg) sometimes (1993) occur in the SPM collected in the anoxic water layer. The highest concentrations of Zn occur just below the redoxcline at 22 m water depth (in 1993), and copper, lead and cadmium have maximum concentrations between 30 and 80 m depth, where the amount of total SPM is at a minimum (about 0.3 mg/L). On a mass per volume (g/L) basis, the maximum concentrations of Cd, Cu and Fe occur at the interface (21m) and those of Zn occur just below the redoxcline (22 m depth). The SPM and sediment trap data suggest that the metals are precipitated as sulfide minerals in the anoxic water. The presence of particulate sulfides was confirmed by SEM studies that show the occurrence of discrete metal (Cu, Fe, Pb, and Zn) sulfide particles in size from 10–20 m as well as framboidal pyrites (1–5 m in size). Higher levels of metal sulfides at intermediate depths rather than in the deep water of Framvaren (> 100 m), may be due to input of trace metals by water exchange over the sill in the upper part of the water column. In the deep water, less metal sulfide precipitation takes place due to depletion of trace metals, and the dilution of particulate metal concentrations by organic matter and by the chemogenic formation of calcite.  相似文献   

Mineralogy, geochemistry, and Nd isotope composition of the Rainbow hydrothermal field, Mid-Atlantic Ridge   总被引：3，自引：0，他引：3  

A. F. A. Marques  F. Barriga  V. Chavagnac  Y. Fouquet 《Mineralium Deposita》2006,41(1):52-67

Petrological, geochemical, and Nd isotopic analyses have been carried out on rock samples from the Rainbow vent field to assess the evolution of the hydrothermal system. The Rainbow vent field is an ultramafic-hosted hydrothermal system located on the Mid-Atlantic Ridge characterized by vigorous high-temperature venting (∼365°C) and unique chemical composition of fluids: high chlorinity, low pH and very high Fe, and rare earth element (REE) contents (Douville et al., Chemical Geology 184:37–48, 2002). Serpentinization has occurred under a low-temperature (<270°C) retrograde regime, later overprinted by a higher temperature sulfide mineralization event. Retrograde serpentinization reactions alone cannot reproduce the reported heat and specific chemical features of Rainbow hydrothermal fluids. The following units were identified within the deposit: (1) nonmineralized serpentinite, (2) mineralized serpentinite—stockwork, (3) steatite, (4) semimassive sulfides, and (5) massive sulfides, which include Cu-rich massive sulfides (up to 28wt% Cu) and Zn-rich massive sulfide chimneys (up to 5wt% Zn). Sulfide mineralization has produced significant changes in the sulfide-bearing rocks including enrichment in transition metals (Cu, Zn, Fe, and Co) and light REE, increase in the Co/Ni ratios comparable to those of mafic Cu-rich volcanic-hosted massive sulfide deposits and different ¹⁴³Nd/¹⁴⁴Nd isotope ratios. Vent fluid chemistry data are indicative of acidic, reducing, and high temperature conditions at the subseafloor reaction zone where fluids undergo phase separation most likely under subcritical conditions (boiling). An explanation for the high chlorinity is not straightforward unless mixing with high salinity brine or direct contribution from a magmatic Cl-rich aqueous fluid is considered. This study adds new data, which, combined with the current knowledge of the Rainbow vent field, brings compelling evidence for the presence, at depth, of a magmatic body, most likely gabbroic, which provides heat and metals to the system. Co/Ni ratios proved to be good tools used to discriminate between rock units, degree of sulfide mineralization, and positioning within the hydrothermal system. Deeper units have Co/Ni <1 and subsurface and surface units have Co/Ni >1.  相似文献   

362℃和差异应力条件下硫化物在NaCl溶液中的再活化实验研究   总被引：2，自引：3，他引：2  

顾连兴汤晓茜  王子江郑远川吴昌志  陆建军倪培　吴学益 《岩石学报》2005,21(5):1429-1434

红透山块状硫化物矿石主要成分为黄铁矿、磁黄铁矿、黄铜矿、闪锌矿和石英、角闪石、黑云母等脉石矿物。切成长40mm 直径17mm 的矿石圆柱用20wt%NaCl 溶液浸泡260小时后装入长江500型活塞-圆筒式三轴应力试验机,在362℃414MPa 围压下加1342MPa 轴压,13小时后于空气中自然冷却。实验后试样长度压缩为32.3mm,算得应变速率为4.1×10~(-6)/s。实验产物中出现大量垂直应力轴的松弛裂缝。黄铁矿强烈脆性破裂,而磁黄铁矿、黄铜矿和闪锌矿以塑性变形为主,局部也发生脆性破裂。再活化黄铁矿、磁黄铁矿和黄铜矿分别充填同种矿物的碎粒间隙。再活化产物也呈细脉穿插脆性变形的黄铁矿碎斑,细脉中以黄铜矿为主,其次是磁黄铁矿,有时含极少量闪锌矿,在磁黄铁矿、黄铜矿和闪锌矿的塑性变形区内,以及变形的石英和其它脉石矿物中均无再活化硫化物产出。实验结果表明在构造应力作用下强干性矿物和地质体容易发生脆性变形,从而为再活化成矿流体的运移和析出矿质提供通道和空间,而韧性变形区较难提供流体通道和矿质沉淀空间。所以,再活化成矿作用容易发生在脆性变形区和韧-脆性转换部位。原生矿石中的黄铜矿在实验条件下比其它三种硫化物更容易再活化。脆性变形的黄铜矿和黄铁矿比起其它矿物来更容易接受含铜流体的叠加,因此地层中的含铜黄铁矿矿胚层最容易受叠加流体作用而形成层控富矿床。  相似文献   

Sulfur Content and Isotopic Ratio of Cambro-Ordovician Carbonate Rocks from South Korea: A Possible Source for Mesozoic Magmatic-hydrothermal Ore Sulfur     

Shunso ISHIHARA  Myung–Shik JIN  Yoshimichi KAJIWARA 《Resource Geology》2002,52(1):41-48

Abstract: Carbonate rocks of Cambrian (18 samples) and lower-middle Ordovician (11 samples) ages from South Korea were analyzed for sulfur contents of structurally substituted sulfate (SSS) and sulfides and their δ³⁴S values. The δ³⁴S values of SSS ranging from +25.9 to +45.2 permil, are averaged as +33.6 and +33.5 permil for the Cambrian and Ordovician rocks, respectively, which indicate high δ³⁴S values of the Cambro-Ordovician seawater. The SSS contents in the carbonate rocks are low being 2.9 to 17.3 ppm S (averaged as 7.0 ppm S). Sulfide sulfur, on the contrary, is much abundant containing 3 to 1,880 ppm S and the δ³⁴S values range widely between –17.6 and +31.1 permil. Sulfide sulfur of the studied rocks excluding impure carbonates has an average content of 187 ppm S and δ³⁴S value of +12.8 permil (n=24). The estimated δ³⁴S (sulfate–sulfide) values, which range from 13.8 to 25.4 permil in general with a few exceptions from 36.5 up to 52.3 permil for some impure carbonates, may provide evidence for the persistent oceanic anoxia with its temporary recovery during the Cambro-Ordovician time.
The SSS and sulfide sulfurs have often higher δ³⁴S values than the Mesozoic-Cenozoic ore sulfur (Ishihara et al., 2000). Since carbonate rocks are very reactive with circulating hydrothermal ore solution, high δ³⁴S values of the Korean ore deposits might be caused to some extent by ³⁴S enrichment from the host carbonates, resulting in the low SSS contents observed.  相似文献   

建德铜矿床的海底喷流沉积成因   总被引：2，自引：0，他引：2  

刘家军  李元林 《矿产与地质》1996,10(3):145-154

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  相似文献   

辽宁红透山铜锌块状硫化物矿床的变质变形和成矿组分再活化   总被引：9，自引：5，他引：9  

顾连兴汤晓茜  郑远川吴昌志田泽满  陆建军肖新建 倪培 《岩石学报》2004,20(4):923-934

辽宁红透山铜-锌块状硫化物产在太古宙绿岩带中，矿床形成后经历了强烈的变形和变质，变质程度达高级角闪岩相。野外和显微镜研究表明，矿石在进变质过程中发生过强烈的机械再活化和重结晶，但各种进变质结构大部分已被变质峰期的全面重结晶所清除，目前保存着的结构主要是变质峰期和退变质过程的产物。退变质过程以黄铁矿变斑晶生长、矿石糜棱岩的形成、二次退火和化学再活化为特征。矿床中高度富集铜和金的矿石是韧性剪切形成的矿石糜棱岩受退变质流体叠加而成。磁黄铁矿主要是同生沉积后重结晶的产物，另有一部分由退变质热液形成，而黄铁矿变斑晶则有沉积一重结晶、磁黄铁矿退变质脱硫和热液叠加多种成因。世界各地块状硫化物矿床中的磁黄铁矿和黄铁矿各有三种成因类型。磁黄铁矿的类型有：同生沉积．变质重结晶、同生沉积黄铁矿变质和退变质热液充填或交代；黄铁矿的类型有：同生沉积-变质重结晶、磁黄铁矿退变质脱硫和退变质热液充填或交代。红透山矿区的退变质流体具有从早到晚氧逸度升高的趋势。  相似文献