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   

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   

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   

Kinetics of sulfide mineral oxidation in seawater: Implications for acid generation during in situ mining of seafloor hydrothermal vent deposits     

《Applied Geochemistry》2016

  相似文献   

News from the seabed – Geological characteristics and resource potential of deep-sea mineral resources     

《Marine Policy》2016

Marine minerals such as manganese nodules, Co-rich ferromanganese crusts, and seafloor massive sulfides are commonly seen as possible future resources that could potentially add to the global raw materials supply. At present, a proper assessment of these resources is not possible due to a severe lack of information regarding their size, distribution, and composition. It is clear, however, that manganese nodules and Co-rich ferromanganese crusts are a vast resource and mining them could have a profound impact on global metal markets, whereas the global resource potential of seafloor massive sulfides appears to be small. These deep-sea mineral commodities are formed by very different geological processes resulting in deposits with distinctly different characteristics. The geological boundary conditions also determine the size of any future mining operations and the area that will be affected by mining. Similarly, the sizes of the most favorable areas that need to be explored for a global resource assessment are also dependent on the geological environment. Size reaches 38 million km² for manganese nodules, while those for Co-rich crusts (1.7 million km²) and massive sulfides (3.2 million km²) are much smaller. Moreover, different commodities are more abundant in some jurisdictions than in others. While only 19% of the favorable area for manganese nodules lies within the Exclusive Economic Zone of coastal states or is covered by proposals for the extension of the continental shelf, 42% of the favorable areas for massive sulfides and 54% for Co-rich crusts are located in EEZs.  相似文献   

新探明的玻利维亚银沙(Silver Sand)超大型银矿床地质特征和找矿评价     

冯锐  张永明  URIBE Hernan  毛志昊 《矿床地质》2021,40(1):65-81

银沙银矿(Silver Sand silver deposit)是玻利维亚锡矿带内新探明的一个超大型中硫型浅成低温热液银矿床,已探明银金属资源量约1万t,平均银品位约120 g/t,并伴有少量铅、锌、铟、镓。银矿化与中新世中酸性侵入岩和次火山岩有关。矿体赋存于白垩系蚀变褪色石英砂岩中的密集构造裂隙带内。成矿作用可以划分为原生硫化物成矿期和表生氧化期,原生硫化物成矿期大致可分为3个矿化蚀变阶段,矿化蚀变阶段Ⅰ为大面积绢云母化褪色蚀变及玻利维亚型层状(manto)锡矿化、矿化蚀变阶段Ⅱ为细脉状和构造角砾间含银硫盐和硫化物,矿化蚀变阶段Ⅲ为方解石细脉。银沙银矿分布最为广泛的围岩蚀变类型为绢云母化,其次为黄铁矿化,以及少量硅化、碳酸盐化和重晶石化。矿化特征主要表现为在围岩白垩系石英砂岩构造裂隙内成密集含银硫盐和硫化物细脉及角砾岩脉。矿体埋藏浅,规模大,适合大规模露天开采。作为玻利维亚锡矿带的一个组成部分,该矿床形成于活动大陆弧后地区。根据成矿过程特点,文章初步提出银沙银矿的成矿模型,并根据两年以来找矿勘查工作,提出了进一步找矿方向,特别值得关注的是银沙银矿所在的成矿带呈近北北西走向,长约8 km,宽约2.5 km,区内遍布采矿遗迹,通过进一步系统勘探和开发,有望再探明一个世界级银矿区。  相似文献   

金川铜镍硫化物矿床中铂族矿物的主要类型和产出特征:热液蚀变过程中铂族元素的富集机理     

董宇  魏博  王焰 《岩石学报》2021,37(9):2875-2888

金川铜镍硫化物矿床是我国最主要的铂族元素(PGE)资源产地,其矿石受热液蚀变作用影响明显,并产出多种铂族矿物(PGM)。岩浆演化和热液蚀变过程中PGE的迁移富集机制和PGM的成因,一直是研究PGE地球化学行为非常关注的问题。本文对金川铜镍硫化物矿床中PGM的研究发现,其主要类型包括含PGE的硫砷化物(硫砷铱矿)和砷化物(砷铂矿),Pd的铋化物、碲化物和硒化物,以及少量其他铂族矿物。其中,硫砷铱矿可包裹于各种贱金属硫化物(镍黄铁矿、磁黄铁矿和黄铜矿)中,表明硫砷铱矿可能结晶于早期的含As硫化物熔体,随后被包裹于硫化物熔体冷凝分异产生的单硫化物固溶体(MSS)和中间硫化物固溶体(ISS)中。硫化物熔体中的As可能主要通过地壳混染作用加入幔源岩浆。大量铋钯矿(PdBi)呈微细乳滴状包裹于黄铜矿中,为晚期ISS冷凝形成黄铜矿过程中出溶的产物。少量铋钯矿(PdBi_2)呈不规则状充填于矿物裂隙,与次生磁铁矿脉紧密共生,并随矿石的蚀变程度增加,铋钯矿的化学成分由PdBi逐渐向PdBi_2转变,表明这部分铋钯矿为后期热液蚀变产物。铋碲钯矿和钯的硒化物则主要产出于镍黄铁矿裂隙且与次生磁铁矿紧密共生,指示明显的热液成因。钯的硒化物的出现表明,岩浆期后酸性、高盐度、高氧逸度的富Cl~-流体对金川铜镍硫化物矿床中Pd的迁移和富集起到了关键控制作用。  相似文献   

四川盆地东部中二叠统茅口组热液活动特征          下载免费PDF全文

李红  王良军  柳益群  曾韬  张冬冬  李文厚  周鼎武  杨康  董杨坤  彭毅峰 《古地理学报》2021,23(1)

四川盆地中二叠统茅口组存在丰富的热液流体活动。在野外剖面和岩心观察的基础上,利用多种分析测试方法,对四川盆地东部茅口组碳酸盐岩中的热液活动特征进行了探讨。研究区茅口组热液活动包括2类,一类为硅质热液,表现为薄层硅质岩或硅质团块;另一类为碳酸盐型热液,表现为粗晶方解石和白云石充填在张性构造裂缝中或呈"雪片状"集合体,偶见少量黄铁矿、闪锌矿等金属硫化物伴生。硅质岩主量元素之间的关系表明硅质来源具有多样性,是热液硅与壳源硅的混合;黄铁矿、闪锌矿原位S同位素δ34S介于-3.91‰~-6.87‰之间,推测可能受到了微生物和基性岩浆岩的双重影响;方解石脉和具鞍状双晶的白云石脉普遍具有Ca O高于标准计量、相对富Sr和U、贫REE和Ti、Ce/Ce*明显负异常、Eu/Eu*主体正异常、Y正异常等特征,表明碳酸盐脉为热液活动的产物,流体来源也呈现出火山活动相关流体与富钙地下水混合的特点。闪锌矿富集Ge和Cd,Zn/Cd及Zn/Fe值反映了中等成矿温度。硅质岩和碳酸盐流体包裹体均一温度变化范围较大,介于54.7~294.3℃之间,与稀土元素和微量元素比值所揭示的特征吻合。研究结果表明,穿层状硅质结核和团块的首次出现往往标志着茅口组热液活动的开始,而张性构造裂缝和碳酸盐型热液活动带来的围岩白云化作用则有效地改善了白云岩储集层的物性。  相似文献   

Biomarkers in sedimentary sulfides of precambrian age     

Bernd Mycke  Walter Michaelis  Egon T. Degens 《Organic Geochemistry》1988,13(4-6)

Samples of the Mt Isa formation (Australia, c, 1.5 Ga), and the Shungit formation (U.S.S.R., c. 2.3 Ga) were studied by organic geochemical means. All samples were freed of any low-molecular-weight solvent soluble organic material in order to insure the authenticity of the analysed material. The isolation of biochemical compounds entrapped in sulfides was the major goal of this work.Organic compounds that were entrapped during the early stages of sulfide formation may obviously survive extended periods of time and can be released by a mild hydrogenation of the sulfides. Preliminary investigations of the hydrocarbon fraction indicate n-alkanes, monomethylalkanes, cycloalkanes, and an unknown series of branched alkanes as major constituents. Their distribution patterns show great selectivity with respect to structures and chain lengths of individual compounds. Differences between the hydrogenation reaction product and the sample extract may arise from the release of a different kind of lipid material through dissolution of the sulfides.  相似文献