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1.
The basalt-hosted Wocan Hydrothermal Field (WHF), located on the NW slope of an axial volcanic ridge at a depth of ∼3000 m at 6°22′N on the slow-spreading Carlsberg Ridge, northwest Indian Ocean, was discovered in 2013 during Chinese DY28th cruise. Preliminary investigations show that the field consists of two hydrothermal sites: Wocan-1, which shows indications for recent high-temperature hydrothermal activity, is located near the peak of the axial volcanic ridge at a water depth of 2970–2990 m, and Wocan-2 site, located at a water depth of 3100 m, ∼1.7 km to the northwest of Wocan-1. The recovered hydrothermal precipitates can be classified into four groups: (i) Cu-rich chimneys; (ii) Cu-rich massive sulfides; (iii) Fe-rich massive sulfides; and (iv) silicified massive sulfides. We conducted mineral texture and assemblage observation and Laser-ablation ICP-MS analyses of the hydrothermal precipitates to study the mineralization processes. Our results show that there are distinct systematic trace element distributions throughout the different minerals in the four sample groups. In general, chalcopyrite from the group (i) is enriched in Pb, As, Mo, Ga, Ge, V, and Sb, metals that are commonly referred to as medium- to low-temperature elements. In contrast these elements are present in low contents in the chalcopyrite grains from other sample groups. Selenium, a typical high-temperature metal, is enriched in chalcopyrite from groups (ii) and (iv), whereas Ag and Sn are enriched only in some silicified massive sulfides. As with chalcopyrite, pyrite also shows distinct trace element associations in grains with different habitus. The low-temperature association of elements (Pb, Mo, Mn, U, Mg, Ag, and Tl) is typically present in colloform/framboidal pyrite, whereas the high-temperature association (Se, Co, and Bi) is enriched in euhedral pyrite. Sphalerite in the groups (i) and (iii) at Wocan-1 is characterized by high concentrations of Ga, Ge, Pb, Cd, As, and Sb, indicating that sphalerite in these sample groups likely precipitated at intermediate temperatures. Early bornite, which mainly occurs in the central part of the Cu-rich chimney, is typically enriched in Sn and In compared to the other minerals. In contrast, late bornite that likely formed during increasing interaction of hydrothermal fluids with cold, oxygenated seawater has low Sn and In, but significantly higher concentrations of Ag, Au, Mo and U. Digenite, also forming in the exterior parts of the samples during the late stages of hydrothermal fluid venting, is poor in most trace elements, except Ag and U. The notable Ag enrichment in the late-stage mineral assemblages at both Wocan-1 and Wocan-2 may therefore be related to lower temperatures and elevated pH. Our results indicate that Wocan-1 has experienced a cycle of heating with Cu-rich chimney growth and subsequent cooling, followed by late seafloor weathering, while Wocan-2 has seen intermediate- to high-temperature mineralization followed by intense silicification of sulfides. Seafloor weathering processes or mixing of hydrothermal fluids with seawater during the waning stages of hydrothermal fluid flow result in significant redistributions of trace elements in sulfide minerals.  相似文献   

2.
Re-Os data and PGE concentrations as well as Mo concentrations and isotope data are reported for suites of fine clastic sediments and black shales from the Barberton Greenstone Belt, South Africa (Fig Tree and Moodies Groups, 3.25-3.15 Ga), the Belingwe Greenstone Belt, Zimbabwe (Manjeri Formation, ca. 2.7 Ga) and shales from the Witwatersrand, Ventersdorp and Transvaal Supergroups, South Africa ranging from 2.95 to 2.2 Ga. Moderately oxidizing conditions are required to mobilize Re and Mo in the environment, Mo fractionation only occurs in solution, and these parameters thus have potential use as paleoredox proxies for the early Earth.PGE + Re abundance patterns of Barberton Greenstone Belt sediments are uniform and very similar in shape to those of komatiites. This indicates (1) that the PGE came from a source of predominantly ultramafic composition and, (2) that PGE were transported and deposited essentially in particulate form. Sediments from the younger Belingwe Greenstone Belt show more fractionated PGE + Re patterns and have Re/Os ratios 10 to 100× higher than those of Barberton sediments. Their PGE abundance patterns and Re/Os ratios are intermediate between those of the mid-Archean shales and Neoproterozoic to Recent black shales. They reflect scavenging of Re from solution in the sedimentary environment.δ98/95Mo values of black shales of all ages correlate with their concentrations. The Barberton Greenstone Belt samples have ∼1-3 ppm Mo, similar to a granitoid-basaltic source. This Mo has δ98/95Mo between −1.9 and −2.4‰ relative to present day mean ocean water molybdenum, MOMO and is thus not isotopically fractionated relative to such a source. Similar to the PGE this indicates transport in solid form. Sediments from the Belingwe Greenstone Belt show in part enhanced Mo concentrations (up to 6 ppm) and Mo isotope fractionation (δ98/95Mo up to −1.4‰ relative to MOMO). The combined PGE + Re and Mo data show mainly reducing conditions in the mid-Archean and suggest that by 2.7 Ga, the atmosphere and oceans had become more oxidizing.Substantially younger samples from the Transvaal Supergroup (to ca. 2.2 Ga) surprisingly have mainly low Mo concentrations (around 1 ppm) and show no significant Mo isotope fractionation relative to the continental source. Among possible explanations for this are a return to reducing atmospheric conditions after 2.7 Ga, reservoir effects, or Mo removal by sulfide precipitation following sulfate reduction in early Proterozoic oceans.  相似文献   

3.
The geotectonic units of Zhejiang Province include the Yangtze Plate in the northwest juxtaposed against the South China fold system in the southeast along the Jiangshan–Shaoxing fault. The South China fold system is further divided into the Chencai–Suichang uplift belt and the Wenzhou–Linhai geotectogene belt, whose boundary is the Yuyao–Lishui fault. The corresponding metallogenic belts are the Mo–Au(–Pb–Zn–Cu) metallogenic belt in northwest Zhejiang, the Chencai–Suichang Au–Ag–Pb–Zn–Mo metallogenic belt, and the coastal Ag–Pb–Zn–Mo–Au metallogenic belt. The main Mesozoic metal ore deposits include epithermal Au–Ag(Ag), hydrothermal vein-type Ag–Pb–Zn(Cu), and porphyry–skarn-type Mo and vein-type Mo deposits. These ore bodies are related to the Mesozoic volcanic-intrusive structure: the epithermal Au–Ag(Ag) deposits are represented by the Zhilingtou Au–Ag deposit and Houan Ag deposit and their veins are controlled by volcanic structure; the hydrothermal vein-type Ag–Pb–Zn deposits are represented by the Dalingkou Ag–Pb–Zn deposit and also controlled by volcanic structure; and the porphyry–skarn-type Mo deposits are represented by the Tongcun Mo deposit and the vein-type Mo deposits are represented by the Shipingchuan Mo deposit, all of which are related to granite porphyries. These metal ore deposits have close spatio-temporal relationships with each other; both the epithermal Au–Ag(Ag) deposits and the hydrothermal vein-type Ag–Pb–Zn deposits exhibit vertical zonations of the metallic elements and form a Mo–Pb–Zn–Au–Ag metallogenetic system. These Jurassic–Cretaceous deposits may be products of tectonic-volcanic-intrusive magmatic activities during the westward subduction of the Pacific Plate. Favourable metallogenetic conditions and breakthroughs in the recent prospecting show that there is great resource potential for porphyry-type deposits (Mo, Cu) in Zhejiang Province.  相似文献   

4.
斑岩型铜钼矿床除主要成矿元素Cu,Mo外,还往往共(伴)生Re,Co,Au,Ag等重要元素,综合回收利用共(伴)生金属具有重大资源及环境效益。通过研究斑岩型铜钼矿床中共(伴)生元素Re,Co,Au,Ag的品位、储量、赋存状态及分布规律,认为Co主要以类质同象形式赋存于黄铁矿中,其分布与黄铁矿密切相关,通常浓集于绢英岩化带外侧;Au,Ag主要以自然金、银与金银系列矿物的形式产出,Au,Ag在不同硫化物中的含量、颗粒粒度以及赋存形式差异很大,Au在各蚀变带均有可能富集,但主要浓集区域是钾化带与石英-绢云母化带;Ag在早期主要以Cu-Ag-Au的形式富集于绢英岩化带,晚期以Pb-Zn-Ag形式赋存于青磐岩化带;Re的分布与绢云母化带的辉钼矿密切相关。  相似文献   

5.
白云鄂博群黑色岩系微量元素地球化学特征及地质意义   总被引：3，自引：1，他引：3  
白云鄂博群位于华北地台北缘,是一套中—新元古代裂谷沉积的产物。尖山组和比鲁特组是其中主要的黑色岩系。对以上两组中的碳质页岩和板岩的Au、Ag、As、Ba、Co、Cu、Hg、Mn、Mo、Ni、P、Pb、V、Zn、U、B、Sb等微量元素和稀土元素进行了较为详细的研究。通过元素含量特征、w(V)/w(V+Ni)、w(Zn)-w(Co)-w(Ni)三元图、稀土配分曲线、w(Ce)/w(La)、Ce和Eu异常、w(La)/w(Yb)-w(Ce)/w(La)和w(La)/w(Yb)-w(ΣREE)图解等方法对其沉积环境特征进行了探讨。微量元素含量分析显示白云鄂博群黑色岩系以富亲铜元素和亲石元素、贫亲铁元素为特征,其中富集Hg、B、As、Mn、Sb、Au、Ag、Pb、P、Ba、U、Mo等多种元素;较高的w(B)反映了黑色岩系沉积于盐度较高的水体中;高的w(V)/w(V+Ni)、w(Ce)/w(La)反映了黑色岩系形成于缺氧的沉积环境中;黑色岩系中Hg、Sb、Ba的富集和w(Zn)-w(Co)-w(Ni)图解中投点大部分靠近热水沉积区域指示了黑色岩系中有热水沉积物的参与;稀土元素配分模式、Ce和Eu异常及w(La)/w(Yb)-w(ΣREE)和w(La)/w(Yb)-w(Ce)/w(La)图解投点在两岩组中的不同特点表明尖山组沉积物以陆源沉积为主,有少量热水沉积物参与;而比鲁特组中热水沉积组分所占比例较大,形成时海水较深。  相似文献   

6.
Summary The study focuses on the mode of occurrence of Au, Ag and Te in ores of the Gaisk, Safyanovsk, Uzelginsk and other volcanic-hosted massive sulfide (VHMS) deposits in the Russian Urals. Minerals containing these elements routinely form fine inclusions within common sulfides (pyrite, chalcopyrite and sphalerite). Gold is mostly concentrated as ‘invisible’ gold within pyrite and chalcopyrite at concentrations of 1–20 ppm. Silver mainly occurs substituted in tennantite (0.1–6 wt.% Ag). In the early stages of mineralization, gold is concentrated into solid solution within the sulfides and does not form discrete minerals. Mineral parageneses identified in the VHMS deposits that contain discrete gold- and gold-bearing minerals, including native gold, other native elements, various tellurides and tennantite, were formed only in the latest stages of mineralization. Secondary hydrothermal stages and local metamorphism of sulfide ores resulted in redistribution of base and precious metals, refining of the common sulfides, the appearance of submicroscopic and microscopic inclusions of Au–Ag alloys (fineness 0.440–0.975) and segregation of trace elements into new, discrete minerals. The latter include Au and Ag compounds combined with Te, Se, Bi and S. Numerous tellurides (altaite, hessite, stützite, petzite, krennerite etc.) are found in the massive sulfide ores of the Urals and appear to be major carriers of gold and PGE in VHMS ores.  相似文献   

7.
Bulk compositions of metallic Fe-Ni from two equilibrated ordinary chondrites, Jilin (H5) and Anlong (H5), and two unequilibrated ones, GRV 9919 (L3) and GRV 021603 (H3), were analyzed by inductively coupled plasma mass spectrometry (ICP-MS). The CI-, Co-normalized abundances of siderophile and chalcophile elements of metallic Fe-Ni from the unequilibrated ordinary chondrites correlate with 50% condensation temperatures (i.e., volatility) of the elements. The refractory siderophile elements (i.e., platinum group elements, Re), Au, Ni and Co show a flat pattern (1.01×CI Co-normalized), while moderate elements (As, Cu, Ag, Ga, Ge, Zn) decrease with volatility from 0.63×CI (Co-normalized, As) to 0.05×CI (Co-normalized, Zn). Cr and Mn show deficit relative to the trend, probably due to their main partition in silicates and sulfides (nonmagnetic). Metallic Fe-Ni from the equilibrated ordinary chondrites shows similar patterns, except for strong deficit of Cr, Mn, Ag and Zn. It is indicated that these elements were almost all partitioned into silicates and/or sulfides during thermal metamorphism. The similar deficit of Cr, Mn, Ag and Zn was also found in iron meteorites. Our analyses demonstrate similar behaviors of W and Mo as refractory siderophile elements during condensation of the solar nebula, except for slight depletion of Mo in the L3 and H5 chondrites. The Mo-depletion of metallic Fe-Ni from GRV 9919 (L3) relative to GRV 021603 (H3) could be due to a more oxidizing condition of the former than the latter in the solar nebula. In contrast, the Mo-depletion of the metallic Fe-Ni from the H5 chondrites may reflect partition of Mo from metal to silicates and/or sulfides during thermal metamorphism in the asteroidal body.  相似文献   

8.
The thermodynamic simulation of the geochemical mobility of Au and Ag during their hydrothermal transfer and precipitation was conducted with regard for the formation of continuous nonideal Au-Ag solid solutions (or AuXAg1?X) alloys) and with the analysis of the effects of principal physicochemical parameters (temperature, pH, redox potential, and the concentrations of sulfide sulfur and chloride ions) on the solubility of Au-Ag alloys of various composition. Predominant Au and Ag complexes and the types of solutions were identified, which are characterized by different extractive ability with respect to these metals. A tendency in the variations in the Au/Ag ratio in the solid phase during the evolution of the hydrothermal process was revealed with regard for various conditions under which Ag sulfides can occur. The possible effect of the AuXAg1?X/solution ratio on the composition of the Au-Ag mineralization was demonstrated, and tendencies in the variations in the composition (fineness) of the alloys during their redeposition were identified.  相似文献   

9.
黄铁矿中的微量元素含量既可提供元素赋存状态的信息,又可示踪热液成矿过程。利用电子探针对龙山金锑矿赋矿地层新鲜板岩、蚀变围岩以及矿石中黄铁矿的多种微量元素进行了分析,研究结果表明:沉积黄铁矿中Au主要以纳米颗粒形式存在;热液黄铁矿中既有固溶体金,也有纳米金。沉积黄铁矿中Co、Ni、Sb、Mn、Te可能以固溶体形式存在,As、Pb、Zn、Cu、Ag以包裹体形式存在;热液黄铁矿中As、Sb、Mn、Te可能以固溶体的形式存在,Co、Ni、Pb、Zn、Cu、Ag以矿物包裹体形式存在。龙山金锑矿至少经历了两个成矿期:早期是由深部的富Ni岩浆流体引发的金、铅、铜、钨矿化,该期矿化强度不大;晚期是以大气降水循环引起的金、锑矿化,是龙山金锑矿的主要成矿期,并大致可分为显微金阶段、次显微金辉锑矿阶段、可见金辉锑矿阶段和辉锑矿阶段4个成矿阶段。  相似文献   

10.
Primary sulfides from cores of holes 957M, 957C, and 957H drilled during the ODP Leg 158 on the active hydrothermal TAG mound (Mid-Atlantic Ridge, 26°08′ N) were examined for the concentration of several elements. Based on 262 microprobe analyses, it has been established that the sulfides are characterized by an extremely heterogeneous distribution of noble metals (Au, Ag, Pt, and Pd) and several associated elements (Hg, Co, and Se). Noble metals are arranged in the following order in terms of decreasing abundance, i.e., concentration level above the detection limit (the number of analyses containing the specific element is given in parentheses): Au (65), Ag (46), Pt (21), and Pd (traces). The associated trace elements make up the following series: Co (202), Hg (132), and Se (49). Main carriers of the “invisible” portion of noble metals are represented by pyrite (Au, Hg), marcasite and pyrite (Ag, Co), sphalerite and chalcopyrite (Pt, Pd), and chalcopyrite (Se). The noble metal distribution in sulfides reveals a lateral zonality: the maximal concentration and abundance of Au in chalcopyrite (or Pt and Ag in chalcopyrite and pyrite) increase from the periphery (Hole 957H) to the center (holes 957C and 957M) of the hydrothermal mound, while the Au distribution in pyrite displays a reversed pattern. The Co distribution increases with depth. This work discusses the vertical zonality in the distribution of elements mentioned above and their response to the evolution of ore genesis.  相似文献   

11.
Sedimentary records of redox-sensitive trace elements hold significant potential as indicators of paleoceanographic environmental conditions. Records of Re can reveal the intensity of past reducing conditions in sediments at the time of deposition, whereas records of Ag may record the magnitude of past diatom fluxes to the seafloor. Confidence in paleoenvironmental reconstruction from records of either metal, however, requires it to have experienced negligible redistribution since deposition. This study examines diagenetic rearrangements of Re and Ag that occur in response to exposure to bottom-water O2 in environments of low sedimentation rate, including Madeira Abyssal Plain turbidites and eastern Mediterranean basin sapropels. Authigenic Re was remobilized quantitatively by oxidation but poorly retained by the underlying sediments. All records are consistent with previous work demonstrating that only a limited reimmobilization of Re occurs preferentially in Corg-rich, reducing sediments. Silver was also mobilized quantitatively by oxidation, but it was subsequently immobilized more efficiently in all cases as sharp peaks immediately into anoxic conditions below active oxidation fronts, and these peaks remain immobile in anoxic conditions during long-term burial. Comparison of Ag, S, and Se records from various cores suggests that Ag is likely to have been immobilized as a selenide, a mechanism previously proposed for Hg in similar situations (Mercone et al., 1999). Coexisting narrow peaks of Ag and Hg with Se offer a means of assessing whether oxidative burndown has ever occurred at the top of Corg- and sulfide-rich sedimentary units. Although these results suggest that caution must be used when inferring paleoenvironmental information from records of Ag and Re in cores with low sediment accumulation rates (<5 cm ka−1), they should not affect the promise that authigenic Ag and Re records hold for paleoenvironmental reconstruction in sediments with higher accumulation rates and where anoxic conditions have been maintained continuously.  相似文献   

12.
金银铂族元素成矿机理的新探索   总被引：7，自引：1，他引：7  
通过对金、银、铂族元素的氢化物，羧基化合物理化性质，贵金属矿物主要和次要化学成分，贵金属矿物的共伴生矿物组合，有关矿物流体包裹体化学成分，类地行星概况，生产实验等相关问题的讨论，认为金、银、铂族元素主要呈单质及其合金氢化物，单质羧基化合物，单质羧基氢化物迁移的。它们随岩浆，热液，热气迁至地壳浅部，由于减压，降温，氧逸度显著加大，Eh、Ph值发生变化，H2，CO逃逸，氧化，形成贵金属的单质及合金矿物，有的还能与硫，硫化氢作用形成贵金属的硫化矿物和硫盐矿物。  相似文献   

13.
氧化还原敏感微量元素对古海洋沉积环境的指示意义   总被引：32，自引：1，他引：31  
海洋的氧化还原条件控制着U、V和Mo等氧化还原敏感微量元素在沉积物或沉积岩中的富集程度,所以可以利用沉积物或沉积岩中这些微量元素的含量来重建古海洋的氧化还原状态和沉积环境。海洋沉积物或沉积岩中U、V和Mo的来源少,除了海水提供外,还有陆源碎屑,不过陆源碎屑提供的那部分含量能够被估计。沉积物埋藏之后这些元素（几乎）不发生迁移,保存了沉积时的组成和含量,能较好地反映沉积环境的特征,是古海洋环境的理想指示。在氧化—次氧化的海水环境中U、V和Mo不会富集,缺氧的条件下U和V富集,而在硫化（含溶解的硫化氢）的沉积环境中U、V和Mo在沉积物中都会强烈地富集。利用这种差异,可以根据沉积物或沉积岩中各种微量元素的含量变化来判别沉积时海水的氧化还原状态。但是,必须注意沉积环境的开放与否、成岩作用及重新氧化作用等对微量元素含量的影响。在利用氧化还原敏感元素进行古环境重建时,应首先评估沉积物或沉积岩中特定元素的来源和贡献,剔除非自生部分的影响,然后利用多元素指标综合判别古环境的氧化还原条件,才能获得可靠的结论。  相似文献   

14.
《Ore Geology Reviews》2011,43(1):32-46
Hydrothermal pyrite contains significant amounts of minor and trace elements including As, Pb, Sb, Bi, Cu, Co, Ni, Zn, Au, Ag, Se and Te, which can be incorporated into nanoparticles (NPs). NP-bearing pyrite is most common in hydrothermal ore deposits that contain a wide range of trace elements, especially deposits that formed at low temperatures. In this study, we have characterized the chemical composition and structure of these NPs and their host pyrite with high-resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED), high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM), analytical electron microscopy (AEM), and electron microprobe analysis (EMPA). Pyrite containing the NPs comes from two types of common low-temperature deposits, Carlin-type (Lone Tree, Screamer, Deep Star (Nevada, USA)), and epithermal (Pueblo Viejo (Dominican Republic) and Porgera (Papua New-Guinea)).EMPA analyses of the pyrite show maximum concentrations of As (11.2), Ni (3.04), Cu (2.99), Sb (2.24), Pb (0.99), Co (0.58), Se (0.2), Au (0.19), Hg (0.19), Ag (0.16), Zn (0.04), and Te (0.04) (in wt.%). Three types of pyrite have been investigated: “pure” or “barren” pyrite, Cu-rich pyrite and As-rich pyrite. Arsenic in pyrite from Carlin-type deposits and the Porgera epithermal deposit is negatively correlated with S, whereas some (colloform) pyrite from Pueblo Viejo shows a negative correlation between As + Cu and Fe. HRTEM observations and SAED patterns confirm that almost all NPs are crystalline and that their size varies from 5 to 100 nm (except for NPs of galena, which have diameters of up to 500 nm). NPs can be divided into three groups on the basis of their chemical composition: (i) native metals: Au, Ag, Ag–Au (electrum); (ii) sulfides and sulfosalts: PbS (galena), HgS (cinnabar), Pb–Sb–S, Ag–Pb–S, Pb–Ag–Sb–S, Pb–Sb–Bi–Ag–Te–S, Pb–Te–Sb–Au–Ag–Bi–S, Cu–Fe–S NPs, and Au–Ag–As–Ni–S; and (iii) Fe-bearing NPs: Fe–As–Ag–Ni–S, Fe–As–Sb–Pb–Ni–Au–S, all of which are in a matrix of distorted and polycrystalline pyrite. TEM-EDX spectra collected from the NPs and pyrite matrix document preferential partitioning of trace metals including Pb, Bi, Sb, Au, Ag, Ni, Te, and As into the NPs. The NPs formed due to exsolution from the pyrite matrix, most commonly for NPs less than 10 nm in size, and direct precipitation from the hydrothermal fluid and deposition into the growing pyrite, most commonly for those > 20 nm in size. NPs containing numerous heavy metals are likely to be found in pyrite and/or other sulfides in various hydrothermal, diagenetic and groundwater systems dominated by reducing conditions.  相似文献   

15.
A routine method for the direct determination of Au and associated trace metals in sulfides has been developed for use with a low-flux nuclear reactor (SLOWPOKE II Reactor Facility, University of Toronto). Small samples (100–200 mg) are analysed simultaneously for Au, Ag, As, Sb, Mo, Co, Se, Cd, Fe, and Zn. Sulfides containing finely divided gold can be analysed with a high degree of precision and yield results which agree closely with commercial fire assay-atomic absorption analyses for Au. Favourable comparisons with other analytical techniques (flameless atomic absorption and emission spectrometry) are also indicated for Ag, As, and Sb. Neutron activation has the advantage of providing precise and accurate results for these elements without chemical separation or preconcentration. Analyses of 10 sulfide-bearing reference materials from CANMET, Ottawa are compared with published best values for selected trace metals including Au.  相似文献   

16.
The paper presents data on the geographic and geological conditions of modern sedimentation in Lake Untersee, the largest lake in East Antarctica. Geochemical and sedimentation data indicate that the leading mechanism providing Al-Si sedimentary material to the surface layer of the bottom sediments is the seasonal melting of the Anuchin glacier and the mountain glacier on the southeastern face of the valley hosting the lake. The strongly reduced conditions in the lowermost 25 m of the water column in the smaller of the two depressions at the lake bottom were favorable for the enrichment of the bottom sediments in bacteriogenic organic matter, Mo, Au, and Pd. The H2S-contaminated water facilitates the significant enrichment of the sediments only in redox-sensitive elements able to migrate in the form of anionic complexes and precipitate (coprecipitate) as sulfides.  相似文献   

17.
Concentrations of Ag, Au, Cd, Co, Re, Zn and Platinum-group elements (PGE) have been determined in sulfide minerals from zoned sulfide droplets of the Noril’sk 1 Medvezky Creek Mine. The aims of the study were; to establish whether these elements are located in the major sulfide minerals (pentlandite, pyrrhotite, chalcopyrite and cubanite), to establish whether the elements show a preference for a particular sulfide mineral and to investigate the model, which suggests that the zonation in the droplets is caused by the crystal fractionation of monosulfide solid solution (mss). Nickel, Cu, Ag, Re, Os, Ir, Ru, Rh and Pd, were found to be largely located in the major sulfide minerals. In contrast, less than 25% of the Au, Cd, Pt and Zn in the rock was found to be present in these sulfides. Osmium, Ir, Ru, Rh and Re were found to be concentrated in pyrrhotite and pentlandite. Palladium and Co was found to be concentrated in pentlandite. Silver, Cd and Zn concentrations are highest in chalcopyrite and cubanite. Gold and platinum showed no preference for any of the major sulfide minerals. The enrichment of Os, Ir, Ru, Rh and Re in pyrrhotite and pentlandite (exsolution products of mss) and the low levels of these elements in the cubanite and chalcopyrite (exsolution products of intermediate solid solution, iss) support the mss crystal fractionation model, because Os, Ir, Ru, Rh and Re are compatible with mss. The enrichment of Ag, Cd and Zn in chalcopyrite and cubanite also supports the mss fractionation model these minerals are derived from the fractionated liquid and these elements are incompatible with mss and thus should be enriched in the fractionated liquid. Gold and Pt do not partition into either iss or mss and become sufficiently enriched in the final fractionated liquid to crystallize among the iss and mss grains as tellurides, bismithides and alloys. During pentlandite exsolution Pd appears to have diffused from the Cu-rich portion of the droplet into pentlandite.  相似文献   

18.
Mesozoic ore deposits in Zhejiang Province, Southeast China, are divided into the northwestern and southeastern Zhejiang metallogenic belts along the Jiangshan–Shaoxing Fault. The metal ore deposits found in these belts are epithermal Au–Ag deposits, hydrothermal‐vein Ag–Pb–Zn deposits, porphyry–skarn Mo (Fe) deposits, and vein‐type Mo deposits. There is a close spatial–temporal relationship between the Mesozoic ore deposits and Mesozoic volcanic–intrusive complexes. Zircon U–Pb dating of the ore‐related intrusive rocks and molybdenite Re–Os dating from two typical deposits (Tongcun Mo deposit and Zhilingtou Au–Ag deposit) in the two metallogenic belts show the early and late Yanshanian ages for mineralization. SIMS U–Pb data of zircons from the Tongcun Mo deposit and Zhilingtou Au–Ag deposit indicate that the host granitoids crystallized at 169.7 ± 9.7 Ma (2σ) and 113.6 ± 1 Ma (2σ), respectively. Re–Os analysis of six molybdenite samples from the Tongcun Mo deposit yields an isochron age of 163.9 ± 1.9 Ma (2σ). Re–Os analyses of five molybdenite samples from the porphyry Mo orebodies of the Zhilingtou Au‐Ag deposit yield an isochron age of 110.1 ± 1.8 Ma (2σ). Our results suggest that the metal mineralization in the Zhejiang Province, southeast China formed during at least two stages, i.e., Middle Jurassic and Early Cretaceous, coeval with the granitic magmatism.  相似文献   

19.
The Bent Hill massive sulfide deposit and ODP Mound deposit in Middle Valley at the northernmost end of the Juan de Fuca Ridge are two of the largest modern seafloor hydrothermal deposits yet explored. Trace metal concentrations of sulfide minerals, determined by laser-ablation ICP-MS, were used in conjunction with mineral paragenetic studies and thermodynamic calculations to deduce the history of fluid-mineral reactions during sulfide deposition. Detailed analyses of the distribution of metals in sulfides indicate significant shifts in the physical and chemical conditions responsible for the trace element variability observed in these sulfide deposits. Trace elements (Mn, Co, Ni, As, Se, Ag, Cd, Sb, Pb, and Bi) analyzed in a representative suite of 10 thin sections from these deposits suggest differences in conditions and processes of hydrothermal alteration resulting in mass transfer of metals from the center of the deposits to the margins. Enrichments of some trace metals (Pb, Sb, Cd, Ag) in sphalerite at the margins of the deposits are best explained by dissolution/reprecipitation processes consistent with secondary remineralization. Results of reaction-path models clarify mechanisms of mass transfer during remineralization of sulfide deposits due to mixing of hydrothermal fluids with seawater. Model results are consistent with patterns of observed mineral paragenesis and help to identify conditions (pH, redox, temperature) that may be responsible for variations in trace metal concentrations in primary and secondary minerals. Differences in trace metal distributions throughout a single deposit and between nearby deposits at Middle Valley can be linked to the history of metal mobilization within this active hydrothermal system that may have broad implications for sulfide ore formation in other sedimented and unsedimented ridge systems.  相似文献   

20.
The sediments of City Park Lake (Baton Rouge, Louisiana, USA) are characterized by Pb concentrations that exceed the corresponding National Oceanic and Atmospheric Administration probable effect level by more than a factor of two and concentrations of As, Cd, Cu, Ni and Zn that exceed the corresponding threshold effect levels. The sediments of the lake are likely to be dredged because of concern over shoaling of the lake. There is concern that exposing these sediments to an oxidizing environment could mobilize toxic metal(loid)s that are effectively sequestered under reducing conditions. To address this concern, mixtures of sediments collected from seven locations in City Park Lake were incubated in microcosms under controlled oxidizing and reducing conditions. The slurries were sampled at time intervals over a period of nearly 750 h, and the dissolved Fe, Mn and trace metal concentrations determined. Eh and pH were negatively correlated, with Eh declining by 600 mV per unit increase in pH. Of the toxic metals, only the concentration of Cu was positively correlated with Eh, apparently because of the sequestration of Cu as a very insoluble sulfide precipitate under low Eh conditions. Precipitation of the other metals as sulfides was evidently insignificant because of the low S content of the sediments. Concentrations of the remaining potentially toxic metals were negatively correlated with Eh, apparently because of their sequestration as oxides and/or adsorption to Fe oxides or oxy-hydroxides. Concentrations of Ca, Mg, and Sr were positively correlated with Eh, presumably because of their sequestration in carbonate precipitates under low Eh/high pH conditions.  相似文献   

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