豫西骆驼山硫多金属矿床的成因——来自纹层状矿石中硫化物LA-ICP-MS微量元素证据   总被引：1，自引：1，他引：0  

邢波  向君峰  叶会寿  陈小丹  张国苏  杨晨英  金雪  胡志中 《矿床地质》2017,36(1):83-106

骆驼山硫多金属矿床位于豫西栾川钼多金属矿集区,矿体主要呈似层状和透镜状产于新元古界栾川群三川组和南泥湖组的层间断裂带内的矽卡岩中,受NWW向层间断裂带的控制。该矿床在成因方面的争论的焦点在于:是否存在元古代的喷流沉积成矿作用?具有纹层状构造的硫化物矿石以往被认为是喷流沉积成因矿床的关键证据,但这种矿石结构也可能为热液交代成因。通过详细的野外地质观察,纹层状矿石在空间上主要产于矽卡岩与致密块状硫化物矿石之间,在透辉石长英角岩、矽卡岩及大理岩等围岩中也有分布,纹层状矿石交代了矽卡岩。针对纹层状矿石中的金属硫化物开展LA-ICP-MS原位微区分析,结果表明:(1)闪锌矿形成于中高温环境,其微量元素以富Fe、Mn、In、Co(均值分别为8.5%、6144×10~(-6)、321×10~(-6)和28.54×10~(-6)),贫Ga、Ge、Tl(均值分别为4.31×10~(-6)、0.98×10~(-6)和0.0476×10~(-6))等元素为特征;(2)磁黄铁矿和黄铁矿的微量元素组成均具有富Co(均值分别为57.75×10~(-6)和2787.68×10~(-6))、贫Ni(均值分别为19.24×10~(-6)和11.29×10~(-6))的特征,二者的Ni-Co关系图指示其与岩浆热液密切相关。以地质现象为基础,结合硫化物原位微区分析数据,笔者认为骆驼山硫多金属矿床中的纹层状矿石属于岩浆热液成因。  相似文献   

Geological setting of the Rapu Rapu gold-rich volcanogenic massive sulfide deposits,Albay Province,Philippines     

Ross?L.?SherlockEmail author  Timothy?J.?Barrett  Peter?D.?Lewis 《Mineralium Deposita》2003,38(7):813-830

Gold-rich Fe–Cu–Zn volcanogenic massive sulfide deposits occur within strata of probable Jurassic age on Rapu Rapu Island in Albay Province, Philippines. Massive sulfides at the Ungay Malobago and Hixbar deposits are spatially associated with dacitic volcanic rocks within a highly-deformed sequence of mafic volcanic and quartzofeldspathic sedimentary rocks. The massive sulfide deposits formed at the stratigraphic contact between footwall dacites and hangingwall mafic volcanic and quartzofeldspathic rocks. The deposits and their host strata have undergone regional metamorphism with strong penetrative deformation. Metamorphic mineral assemblages and textural evidence suggest that peak metamorphism was upper-greenschist to lower-amphibolite grade and syn-D₁ deformation. Based on the age of regional metamorphism, deformation is inferred to be mid-Tertiary in age. Deformation at Rapu Rapu resulted in reorientation of the strata into a broad antiform with strong shallow-plunging elongation fabrics, overturning of the volcanic sequence that hosts the Ungay Malobago deposit, and complex folding of the mineralized zones. The present highly linear form of the Ungay Malobago deposit is mainly a product of this ductile strain.Immobile element ratios for a given lithology generally remain constant in saprolitic samples, and thus provide an effective identification tool even in strongly weathered rocks. Lithogeochemical data define a bimodal volcanic suite that is comparable to bimodal assemblages that occur in several modern back-arc basins in the southwestern Pacific Ocean, including those behind the Vanuatu and the New Britain arcs. On Rapu Rapu, the dacitic rocks are enriched in light REE and have high Zr/Y ratios, which indicates a calc–alkaline affinity and suggests a mature island-arc setting. The quartzofeldspathic sedimentary rocks are more widespread than the dacites and have notably lower Zr/Y ratios; they may have been derived from erosion of a distant volcanic arc. The mafic volcanic rocks are dominantly low-K arc tholeiites of basaltic to andesitic composition, but with modest enrichment in the light REE; comparable rocks can be found in the Vanuatu and New Britain back-arc basins.Electronic Supplementary Material Supplementary material is available in the online version of this article at http://dx.doi.org/10.1007/s00126-003-0349-0An erratum to this article can be found at Editorial handling: O. Christensen  相似文献   

The Acoje Block Platiniferous Dunite Horizon, Zambales Ophiolite Complex, Philippines: Melt Type and Associated Geochemical Controls   总被引：3，自引：0，他引：3  

Graciano P. YUMUL Jr. 《Resource Geology》2001,51(2):165-174

Abstract: The Zambales Ophiolite Complex, a supra-subduction zone ophiolite, is made up of the mid-ocean ridge-related Coto block and the island arc-related Acoje block. This crust-mantle sequence hosts platinum-group elements (PGE) in the Acoje block. The melts responsible for the PGE-bearing nickel sulfide and chromitite deposits are of magmatic origin characterized by high-MgO basalt to boninitic composition which, being second or third-stage melts, carry higher PGE budgets. Metal ratio diagrams, utilizing base and precious metals, reveal that the distribution and deposition of the PGE in the Acoje block are affected by olivine, chromite and sulfide crystallization. The generation, accumulation and segregation of the PGE, oxide and sulfide minerals from the melts are governed by the combined factors of high degrees of partial melting, multiple melt replenishment with concomitant magma mixing and fractional crystallization. Although previous sulfide segregation events could have occurred below the PGE-bearing nickel sulfide horizon as shown by the Ni/Cu (>1), the Cu/Pd and Ni/Pd strongly suggest that the main platiniferous zone is confined within the Acoje block transition zone dunite.  相似文献   

On the relationship between auriferous talc deposits hosted in volcanic rocks and massive sulphide deposits in Egypt     

Nagy Shawky Botros 《Ore Geology Reviews》2003,23(3-4):223-257

The volcanic-hosted massive sulphide (VHMS) deposits in the Eastern Desert of Egypt (e.g., Um Saki deposit) are associated with Precambrian coarse acid pyroclastic rocks. The upper contacts of the massive sulphide body are sharp and well-defined; while the keel zone to the mineralization is always associated with pervasive alteration, characterized by the presence of septechlorite and talc, associated with variable amounts of carbonate and tremolite. On the other hand, the economic talc deposits in Egypt are hosted intensively altered volcanic rocks. Besides talc, chlorite, carbonates and tremolite that occur in variable amounts in these deposits, anomalously high concentrations of gold are also present.The present study showed that alterations in the talc deposits of Darhib, El Atshan, Abu Gurdi, Egat, Um Selimat and Nikhira are similar to those occurring in the keel zone underlying the VHMS of Um Samuki and that the chemical modifications due to alteration processes (additions of Mg, Fe, Mn and Ca coupled with depletions in silica, alkalies, alumina and titanium) are comparable, even the host rocks are different, thus reflecting a genetic relationship. It is suggested that, the examined localities of talc deposits are hosted in the intensively altered volcanics in the keel zones of volcanogenic massive sulphide deposits. Recently, detailed geophysical prospecting program, including electric (resistivity, self-potential and induced polarization), electromagnetic and magnetic methods, was carried out at Darhib, Abu Gurdi and Um Selimat talc deposits. The quantitative interpretation of these geophysical measurements revealed the presence of subsurface bodies of sulphides. The present distribution of talc and allied minerals in Darhib, El Atshan, Abu Gurdi, Egat, Um Selimat and Nikhira could be explained by a tectonic process in which the coarse acid pyroclastic rocks with massive sulphides have tilted in such way that the footwall rock alterations (talc and allied minerals) are exposed on the present-day surface at these localities. Structural studies are currently under way in an attempt to explain the deformation regime that led to the present situation of talc deposits.Two distinct spatial and mineralogical associations of gold mineralization could be identified in the volcanogenic massive sulphide deposits and their footwall alterations (the keel zone) in the Eastern Desert of Egypt. These are (1) gold–silver–zinc association, and (2) gold–copper association. In the former, gold grades are very low and silver is anomalous. This association occurs typically in the upper levels of the VHMS deposit where low-temperature sulphides are abundant. Gold was deposited because of the mixing between the ascending hot solutions and the sulphate-rich seawater. The upper levels of Um Samuki sulphide body represent this association. Gold–copper association, on the other hand, typically occurs in the footwall altered rocks (the keel zone) and the lowest parts of the massive sulphide body. Gold grades reach up to 5.54 ppm, but the average is 1 ppm. Silver is very low, usually in the range of 4–10 ppm. Lead usually, but not always, accompanies gold in this association. Deposition of gold probably took place due to decreasing of temperature and/or increasing pH of the ascending hot brines. The keel zones at Darhib, Abu Gurdi, El Atshan, Um Selimat, Nikhira and Egat talc mines better represent this association.  相似文献   

Removal of lead minerals from copper industrial flotation concentrates by xanthate flotation in the presence of dextrin     

Jan Drzymala  Janusz Kapusniak  Piotr Tomasik 《International Journal of Mineral Processing》2003,70(1-4):147-155

Potato starch and dextrins resulting from thermolysis of potato starch in the absence of reagents and presence of -amino acids are promising depressants for separation of lead and copper minerals present in the Polish industrial copper concentrates. The polysaccharides were used for differential xanthate flotation of the final industrial concentrates produced by flotation with sulfhydryl collectors in the absence of depressants. The polysaccharides depressed galena and provided froth concentrate rich in chalcocite and other copper minerals as well as cell product containing lead minerals. The best results of separation were obtained in the presence of plain dextrin prepared by a thermal degradation of potato starch. The industrial concentrate containing 18.5% Cu and 5.5% Pb was divided into a froth product containing 38.1% Cu with 77% recovery of copper and a cell product assaying 7.3% Pb with 83% recovery of lead. It was accomplished using 2500 g/t of dextrin, 50g/t of potassium ethyl xanthate, and 50 g/t of frother (α-terpineol). The pH of flotation was 8.0–8.2.  相似文献   

Non-singular time domain BEM with applications to 3D inertial soil–structure interaction     

Dimitris L. Karabalis   《Soil Dynamics and Earthquake Engineering》2004,24(3):281-293

A direct time domain boundary element method is presented based on the Stokes fundamental solutions, discretized in both time and space, and an efficient time step-by-step solution that minimizes the accumulation of errors. A non-singular numerical integration procedure, in the Cauchy sense, is proposed for the generation of the associated influence matrices. This methodology is shown to be efficient for the solution of a number of computationally intensive problems in the area of soil–structure interaction. In addition, an algorithm for the direct calculation of the response of massive foundations to externally applied forces and/or obliquely incident seismic waves is introduced. The accuracy and computational efficiency of the proposed methodologies is established through a number of comparison studies.  相似文献   

安徽铜陵矿集区海西期喷流沉积流体系统时空结构   总被引：20，自引：3，他引：20  

杨竹森  侯增谦  蒙义峰  曾普胜  李红阳  徐文艺  田世洪  王训诚  姚孝德  姜章平 《矿床地质》2004,23(3):281-297

铜陵矿集区是长江中下游成矿带七大矿集区之一，构造上经历了晚古生代的陆缘裂陷、中三叠世的陆-陆碰撞和侏罗纪—白垩纪的陆内构造-岩浆活动。晚石炭世的海底喷流沉积形成了广泛分布的块状硫化物，除部分构成块状硫化物矿床外，还为燕山期中酸性岩浆活动形成的矽卡岩型矿床提供了部分硫和金属物质。为了查明海西期喷流沉积流体系统及其时空展布特征，在铜陵矿集区内开展了以流体活动记录为对象的蚀变-流体填图工作。结果显示，海西期喷流沉积流体系统不仅形成以块状硫化物为主体的喷流沉积记录，而且在下伏岩系中遗留了区域规模的流体蚀变记录。以块状硫化物为主体的喷流沉积记录构成3个喷流沉积旋回，在垂向上和横向上均具有成分和结构的分带性。流体蚀变记录在上部构成顺层蚀变带，在中部构成沿断裂和裂隙充填的石英一硫化物脉体群。在下部则构成半整合蚀变带，表明喷流沉积流体系统由下渗的海水在下部半整合蚀变带形成储集区，经高地热异常的加热后，沿中部脉体群向上迁移，在进入顺层蚀变带后沿砂岩层向两侧扩散，最后经同生断裂和裂隙向海底喷出。块状硫化物与蚀变岩、喷流沉积旋回及硫化物硫同位素的空间展布特征，显示区内存在3个受基底断裂控制的NWW向延伸的流体活动域，包含6个以上的流体储集区域，每个流体储集区域之上发育多个流体上升中心和海底喷流中心。  相似文献   

Pb—Sn—Fe—Sb—S体系相关系     

吴大清 《矿物学报》1989,9(3):232-240

用抽空石英管法研究以Fe_(0·96) Sb_(2·04) S_(4·12)为投影顶点,8×(PbS-SnS-SnS_2)为投影平面的Pb-Sn-Fe-Sb-S体系的相图表明,由于Pb(?)Sn~(2+)之间互相取代,500℃时辉锑锡铅矿固溶体中Sn~(2+)变化范围(以单位分子式11个金属原子总数为计量)是0—4.8个原子,400℃时则为0—4.0个原子。同时,Sn~(4+)变化范围是1.3—2.3个原子和1.5—2.1个原子。圆柱锡矿固溶体变化范围较小。500℃时Sn~(2+)变化范围是0.4—1.8个原子,400℃时为0.5—1.7。Sn~(+4)变化范围则分别为3.2—4.2个原子和3.3—4.2个原子。变更Fe含量(0.81—1.09)及Sb含量(1.83—2.29)进行的几组合成实验表明,上述两个矿物中Fe、Sb含量变化范围很小,不超过±0.15个原子。辉锑锡铅矿固溶体可与方铅矿、块硫锑铅矿、针硫锑铅矿、硫锡铅矿、硫锡矿、圆柱锡矿等形成平衡结线。而圆柱锡矿不与方铅矿、硫锡矿、硫锡铅矿形成平衡结线,但可与辉锑矿、SnS_2及上述其他矿物形成平衡结线。结合锡的硫化物及氧化物(锡石)热力学稳定场计算表明,在本体系内辉锑锡铅矿在300℃时稳定区的硫活度在lga_(s2)=-20(atm)附近,氧活度小于lga_(o2)=-40(atm),而圆柱锡矿稳定区硫活度大于lga_(s2)=-10(atm)。  相似文献   

Diffusion of osmium in pyrrhotite and pyrite: implications for closure of the Re–Os isotopic system     

James M. Brenan  Daniele J. Cherniak  Lesley A. Rose 《Earth and Planetary Science Letters》2000,180(3-4):399-413

In order to better constrain the extent to which common sulfide minerals will retain their osmium isotopic composition subsequent to crystallization, we have conducted experiments to quantify the diffusion behavior of osmium in pyrite and pyrrhotite. Experiments consisted of either (1) isothermal soaking of diffusion couples consisting of natural pyrite or pyrrhotite crystals packed against powdered Os-bearing Fe-sulfide or (2) ‘relaxation’ of initially high near-surface osmium concentrations produced in the latter experiments (pyrite only). Osmium penetration into samples was characterized by depth profiling using Rutherford backscattering spectroscopy (RBS) (pyrite) or electron microprobe analyses across sectioned run products (pyrrhotite). Results of the first type of diffusion experiment involving pyrite show only limited osmium penetration into sample surfaces, with the extent of penetration uncorrelated with run duration. Images of pyrite samples using atomic force microscopy show roughening of initially smooth surfaces as a consequence of step formation and suggest that osmium incorporation into the near-surface occurred by solute uptake during step growth and not by volume diffusion. Prolonged (1000⁺ h) ‘relaxation’ experiments revealed no additional osmium penetration into pyrite surfaces and based on the depth resolution for RBS, a maximum diffusion coefficient of 2.5×10⁻²³ m²/s at 500°C was calculated. Experiments involving pyrrhotite over the temperature range of 950–1100°C showed extensive osmium uptake and osmium concentration gradients that conform with Fickian diffusion behavior. We found that pyrrhotite Fe/S could be varied by changes in the composition of the starting material and osmium source and over the range of Fe/S produced in experiments (molar Fe/S=0.83–0.90), we observed no systematic variation in the osmium diffusion coefficient. Diffusion coefficients measured parallel to the a crystallographic axis were on average 1.4× higher than values measured parallel to c and regression of the c-axis data yielded the Arrhenius relation:The application of these diffusion data to simple models of diffusive exchange during static or polythermal time–temperature histories is used to assess the conditions under which radiogenic osmium will be retained. During isothermal annealing, calculations indicate that the cores of millimeter-sized spherical pyrrhotite crystals undergoing diffusive exchange with an external osmium reservoir will have their initial compositions perturbed in ≤0.5 Ma at temperatures exceeding 400°C. Pyrite undergoing the same process at 500°C requires in excess of 10 Ma before crystal cores are affected. The relatively short ‘core retention’ time-scales for pyrrhotite indicates that this mineral may be prone to isotopic resetting following relatively brief crustal thermal events, thus possibly accounting for the scatter that commonly occurs in Re–Os isochrons generated from massive sulfide samples. Calculated closure temperatures (T_c) for osmium exchange in pyrrhotite yielded values of 300–400°C for grain sizes ranging from 10 to 1000 μm. These values of T_c are similar to those calculated for Ar retention in biotite, and considerably lower than for Sr in apatite and plagioclase, for example. Such low closure temperatures for pyrrhotite suggest this mineral will date the final stage in the cooling of a magmatic system and possibly be susceptible to open system osmium exchange in the presence of late-stage hydrothermal fluids. This latter result infers that caution be applied when interpreting elevated initial osmium isotopic ratios as a product of crustal assimilation at the magmatic stage.  相似文献   

Geology, mineralogy and stable isotope geochemistry of the Kabwe carbonate-hosted Pb–Zn deposit, Central Zambia     

A.F. Kamona  G.H. Friedrich 《Ore Geology Reviews》2007,30(3-4):217-243

The carbonate-hosted Kabwe Pb–Zn deposit, Central Zambia, has produced at least 2.6 Mt of Zn and Pb metal as well as minor amounts of V, Cd, Ag and Cu. The deposit consists of four main epigenetic, pipe-like orebodies, structurally controlled along NE–SW faults. Sphalerite, galena, pyrite, minor chalcopyrite, and accessory Ge-sulphides of briartite and renierite constitute the primary ore mineral assemblage. Cores of massive sulphide orebodies are surrounded by oxide zones of silicate ore (willemite) and mineralized jasperoid that consists largely of quartz, willemite, cerussite, smithsonite, goethite and hematite, as well as numerous other secondary minerals, including vanadates, phosphates and carbonates of Zn, Pb, V and Cu.Galena, sphalerite and pyrite from the Pb–Zn rich massive orebodies have homogeneous, negative sulphur isotope ratios with mean δ³⁴S_CDT permil (‰) values of − 17.75 ± 0.28 (1σ), − 16.54 ± 0.0.27 and − 15.82 ± 0.25, respectively. The Zn-rich and Pb-poor No. 2 orebody shows slightly heavier ratios of − 11.70 ± 0.5‰ δ³⁴S for sphalerite and of − 11.91 ± 0.71‰ δ³⁴S for pyrite. The negative sulphur isotope ratios are considered to be typical of sedimentary sulphides produced through bacterial reduction of seawater sulphate and suggest a sedimentary source for the sulphur.Carbon and oxygen isotope ratios of the host dolomite have mean δ¹³C_PDB and δ¹⁸O_SMOW values of 2.89‰ and 27.68‰, respectively, which are typical of marine carbonates. The oxygen isotope ratios of dolomite correlate negatively to the SiO₂ content introduced during silicification of the host dolomite. The depletion in ¹⁸O in dolomite indicates high temperature fluid/rock interaction, involving a silica- and ¹⁸O-rich hydrothermal solution.Two types of secondary fluid inclusions in dolomite, both of which are thought to be related to ore deposition, indicate temperatures of ore deposition in the range of 257 to 385 and 98 to 178 °C, respectively. The high temperature fluid inclusions contain liquid + vapour + solid phases and have salinities of 15 to 31 eq. wt.% NaCl, whereas the low temperature inclusions consist of liquid + vapour with a salinity of 11.5 eq. wt.% NaCl.Fluid transport may have been caused by tectonic movements associated with the early stages of the Pan-African Lufilian orogeny, whereas ore deposition within favourable structures occurred due to changes in pressure, temperature and pH in the ore solution during metasomatic replacement of the host dolomite. The termination of the Kabwe orebodies at the Mine Club fault zone and observed deformation textures of the ore sulphides as well as analysis of joint structures in the host dolomite, indicate that ore emplacement occurred prior to the latest deformation phase of the Neoproterozoic Lufilian orogeny.  相似文献