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1.
石英(滑石)菱镁岩是基性岩、超基性岩与富CO2流体反应形成的一套硅化-碳酸盐化蚀变岩,常伴生金、汞、菱镁矿、碱金属矿化而在国外备受关注,但国内相关研究较薄弱。巴尔蛇绿岩位于西藏阿里地区,石英菱镁岩主要出露在蛇绿岩体东北边界,出露厚度约20 m,近北西西向延伸数千米。本文系统研究了雅鲁藏布缝合带西段巴尔蛇绿岩边部石英菱镁岩矿物学及地球化学特征。根据尖晶石镜下特征,划分为两个阶段:一阶段石英菱镁岩中尖晶石稳定存在,二阶段石英菱镁岩中尖晶石几乎全部蚀变(代表更强程度蚀变作用)。石英菱镁岩主要地球化学组成为Si O2、Mg O及CO2,8件样品主量元素含量变化较大,Si O2/Mg O比值波动较大,反映石英菱镁岩形成为非等化学过程。蛇纹石化橄榄岩与石英菱镁岩有着相似微量元素分布规律,表明同源性,但两者仍有较明显差异:两阶段石英菱镁岩LREE都较地幔橄榄岩略富集,从地幔橄榄岩到两阶段石英菱镁岩,HREE先亏损再略富集。微量元素标准化图解中,Sr在橄榄岩与石英菱镁岩中都为正异常,其含量随蚀变强度增强而增加。此外,两阶段石英菱镁岩均无Au、Hg矿化。  相似文献   

2.
苏本勋  肖燕  陈晨  白洋  刘霞  梁子  彭青山 《地球科学》2018,43(4):1011-1024
蛇绿岩中铬铁矿床成因一直存在较大争议,其主要原因可归结为:寄主蛇绿岩存在成因争议、产出状态不清、矿石及围岩矿物组合单一以及主要矿物成分简单但矿物包裹体复杂多样.针对这些研究瓶颈,率先对西藏普兰和罗布莎、土耳其K?z?lda?和Kop蛇绿岩中的地幔橄榄岩和铬铁岩进行了全岩和单矿物Fe-Mg同位素的探索性研究工作.结果表明:（1）蛇绿岩中的地幔橄榄岩具有较均一的Fe-Mg同位素组成,与世界上其他地区的地幔橄榄岩相似;（2）铬铁岩中铬铁矿和橄榄石之间存在明显的Fe-Mg同位素分馏,铬铁矿多具有比共存橄榄石轻的Fe同位素组成,与地幔橄榄岩中的尖晶石和橄榄石相反,Mg同位素变化较大;（3）铬铁矿和橄榄石的Fe-Mg同位素主要受控于结晶分异和Fe-Mg交换,且这两个过程造成的同位素变化趋势明显不同.因此,Fe-Mg同位素在揭示铬铁矿母岩浆来源、性质及成矿过程方面具有较大的应用潜力.   相似文献   

3.
Two typical mineral textures of the MG 1 chromitite of the Bushveld Complex, South Africa, were observed; one characterised by abundant orthopyroxene oikocrysts, and the other by coarse-grained granular chromitite with only minor amounts of interstitial material. Oikocrysts form elongate clusters of several crystals aligned parallel to the layering, and typically have subhedral, almost chromite-free, core zones containing remnants of olivine. The core zones are surrounded by poikilitic aureoles overgrowing euhedral to subhedral chromite chadacrysts. Chromite grains show no preferred crystal orientation, whereas orthopyroxene grains forming clusters commonly share the same crystallographic orientation. Oikocryst core zones have lower Mg# and higher concentrations of incompatible trace elements compared to their poikilitic aureoles. Core zones are relatively enriched in REE compared to a postulated parental magma (B1) and did not crystallise in equilibrium with the surrounding minerals, whereas the composition of the poikilitic orthopyroxene is consistent with growth from the B1 magma. These observations cannot be explained by the classic cumulus and post-cumulus models of oikocryst formation. Instead, we suggest that the oikocryst core zones in the MG1 chromitite layer formed by peritectic replacement of olivine primocrysts by reaction with an upwards-percolating melt enriched in incompatible trace elements. Poikilitic overgrowth on oikocryst core zones occurred in equilibrium with a basaltic melt of B1 composition near the magma-crystal mush interface. Finally, adcumulus crystallisation followed by grain growth resulted in the surrounding granular chromitite.  相似文献   

4.
Four natural chromite samples (LBS13-04, LBS13-06 and LBS13-13) from the Luobusa ophiolite (China) and 16SW2-6 from the Stillwater Complex (USA) were developed as reference materials for in situ element microanalysis. Approximately 8 g of chromite fragments with grain sizes of 0.5–1.5 mm from each chromite sample were separated under a binocular microscope and analysed by EPMA, XRF, LA-ICP-MS and solution nebulisation ICP-MS techniques for major and trace elements at six laboratories. The results show that the four chromite samples are homogeneous with respect to MgO, Al2O3, Cr2O3, FeO, Sc, Ti, V, Mn, Co, Ni, Zn and Ga. These samples are thus suitable to be used as reference materials for in situ microanalysis.  相似文献   

5.
江西相山铀矿田邹家山铀矿床蚀变特征及热液来源   总被引：1，自引：0，他引：1  
对江西相山铀矿田邹家山矿床不同标高的赋矿围岩及矿石样品进行了主量元素、微量元素和稀土元素地球化学分析。结果表明,邹家山矿床不同中段的矿石经历了碱性—酸性—碱性的蚀变过程,在-85 m中段酸性蚀变达到最强,随深度增加碱性蚀变呈增强的趋势;微量元素的Q型聚类分析、不同中段U含量分析和稀土元素的配分模式表明,成矿物质可能并不来源于赋矿围岩,而是来源于流纹英安岩岩浆。进一步根据与成矿关系密切的13种元素的R型聚类分析,将邹家山矿床成矿热液系统划分为高温成矿热液系统和中低温成矿热液系统。  相似文献   

6.
Ore mineralization and wall rock alteration of Crater Mountain gold deposit, Papua New Guinea, were investigated using ore and host rock samples from drill holes for ore and alteration mineralogical study. The host rocks of the deposit are quartz‐feldspar porphyry, feldspar‐hornblende porphyry, andesitic volcanics and pyroclastics, and basaltic‐andesitic tuff. The main ore minerals are pyrite, sphalerite, galena, chalcopyrite and moderate amounts of tetrahedrite, tennantite, pyrrhotite, bornite and enargite. Small amounts of enargite, tetradymite, altaite, heyrovskyite, bismuthinite, bornite, idaite, cubanite, native gold, CuPbS2, an unidentified Bi‐Te‐S mineral and argentopyrite occur as inclusions mainly in pyrite veins and grains. Native gold occurs significantly in the As‐rich pyrite veins in volcanic units, and coexists with Bi‐Te‐S mineral species and rarely with chalcopyrite and cubanite relics. Four mineralization stages were recognized based on the observations of ore textures. Stage I is characterized by quartz‐sericite‐calcite alteration with trace pyrite and chalcopyrite in the monomict diatreme breccias; Stage II is defined by the crystallization of pyrite and by weak quartz‐chlorite‐sericite‐calcite alteration; Stage III is a major ore formation episode where sulfides deposited as disseminated grains and veins that host native gold, and is divided into three sub‐stages; Stage IV is characterized by predominant carbonitization. Gold mineralization occurred in the sub‐stages 2 and 3 in Stage III. The fS2 is considered to have decreased from ～10?2 to 10?14 atm with decreasing temperature of fluid.  相似文献   

7.
在西藏罗布莎蛇绿岩块的豆荚状铬铁矿中，存在包裹体矿物镁橄榄石，这些镁橄榄石为无色透明多晶面形成的自形晶，Fo值可达到97－98，具富镁端员组分，选取一代表性颗粒的单晶进行X单晶和衍射分析，表明其为斜方晶系，空间群Pbnm，镁橄榄石晶胞参数,a,b,c以及M1－0和M2－0键长均小于地幔包裹体和一般地幔岩中橄缆中的对应值，测试出的晶胞参数与人工合成镁橄榄石的一致，镁橄榄石具有橄榄石族中已知最小的晶胞参数，据此推断它是在超高压环境下结晶的。  相似文献   

8.
Intergrowth boundaries between mineral individuals in dunite of the Gal’moenan massif in Koryakia was studied in terms of crystal morphology, crystal optics, and ontogenesis. The results obtained allowed us to trace the staged formation of olivine and chromite and four generations of these minerals. Micro-and nanotopography of boundary surfaces between intergrown mineral individuals of different generations was examined with optic, electron, and atomic force microscopes. The boundaries between mineral individuals of different generations are distinguished by their microsculpture for both olivine and chromite grains. Both minerals demonstrate a compositional trend toward refinement from older to younger generations. The decrease in the iron mole fraction in olivine and chromite is accompanied by the crystallization of magnetite along weakened zones in olivine of the first generation and as outer rims around the chromite grains of the second generation observable under optic and electronic microscopes. The subsequent refinement of chromite results in the release of PGE from its lattice, as established by atomic power microscopy. The newly formed PGM are localized at the boundaries between mineral individuals and, thus, mark a special stage in the ontogenetic evolution of mineral aggregates. Further recrystallization is expressed in the spatial redistribution of grain boundaries and the formation of monomineralic intergrowth boundaries, i.e., the glomerogranular structure of rock and substructures of PGM, chromite, and olivine grains as intermediate types of organization of the granular assemblies in the form of reticulate, chain, and cellular structures and substructures of aggregates.  相似文献   

9.
阿拉斯加型岩体的基本特征、成岩过程及成矿作用   总被引：2，自引：2，他引：0  
阿拉斯加型岩体是一类具有独特的岩性环带状结构的镁铁-超镁铁质侵入体,常呈链状分布于汇聚板块边缘。其形成时代跨度较大,从元古代到新生代均有分布,以中生代最为发育。大部分阿拉斯加型岩体规模较小,出露面积约12～14 km~2或更小,平面上呈近似同心环状结构,垂直剖面上呈管道状。岩体中心为纯橄岩,向外依次包括异剥橄榄岩、橄榄单斜辉石岩、单斜辉石岩、角闪单斜辉石岩、角闪石岩和辉长岩。造岩矿物为橄榄石、单斜辉石、角闪石等,副矿物为铬铁矿、磁铁矿、钛铁矿等,超镁铁质岩石中少或无斜方辉石,斜长石仅出现在边缘的辉长质岩石中。磁铁矿在单斜辉石岩和角闪石岩中为常见矿物,含量最高达15%～20%。阿拉斯加型岩体的主量元素成分揭示所有岩石均为与拉斑玄武质岩浆分异有关的亚碱性堆晶岩。微量元素成分上显示平坦的稀土元素配分型式和较低的微量元素含量,且富集大离子亲石元素,亏损高场强元素。矿物化学特征上,橄榄石富镁且Fo值变化较大;单斜辉石主要为富Ca的透辉石,其成分变化具有弧堆晶趋势;角闪石主要是镁角闪石和韭角闪石;铬铁矿富集Fe-Al,贫Cr。这些特征揭示,该类岩体成因明显不同于层状岩体和阿尔卑斯型岩体。综合岩石学、矿物学和地球化学分析表明,阿拉斯加型岩体形成于与板块俯冲作用有关的岛弧或者活动大陆边缘背景下,其母岩浆为受到熔/流体交代的地幔楔部分熔融产生的含水玄武质岩浆。各岩相为未受明显地壳混染的同源母岩浆在地壳深度结晶分异的产物。阿拉斯加型岩体的岩浆体系具有含水且高氧逸度的特征,其通常为铂族元素和铬铁矿矿床的重要载体,无或少铜镍矿化。  相似文献   

10.
The heavy mineral placer deposits of the coastal sediments in south Maharashtra stretch for 12.5 km from Pirwadi in the north to Talashil in the south. The area is a sand bar represented by a narrow submergent coastal plain lying between the Achara and Gad Rivers. The sediments in the area are mainly sands which are moderately well sorted to well sorted. The heavy mineral concentration in the surficial sediments ranges between 0.69 and 98.32 wt % (28.73 wt % in average). The heavy mineral concentration shows an increasing trend from north to south. The heavy mineral suite consists predominantly of opaque minerals (ilmenite, magnetite and chromite), garnet, pyroxene, amphibole, zircon, tourmaline, rutile, staurolite, etc. Ilmenite grains are fresh whereas magnetite grains show the effect of weathering and alteration. The chromite grains are rounded to sub-rounded with alteration at the margin of the grains. The surficial textures of the opaque minerals show mechanical breaking that indicates limited distance of transportation. Ilmenite has TiO2 in the range between 40.04 and 46.6 wt %. Based on ore microscopy studies, the magnetite grains appear to be of two types: pure magnetite and titano-magnetite. Compositionally, the total magnetite fractions have Fe2O3 between 32 and 46 wt %, FeO between 19.0 and 25 wt % and TiO2 between 14.3 and 23.9 wt %. The chromite grains are an admixture of two varieties, ferro-chromite and magnesio-chromite. The chromite grains have 32.06–47.5 wt % of Cr2O3 with total iron between 23.86 wt % (4.73% Fe2O3 and 19.13% FeO) and 27.89 wt % (4.36% Fe2O3 and 23.53% FeO) and MgO between 12 and 40 wt %. The observed variations in the distribution of heavy minerals in the area are due to differences in the sediment supply, their specific gravity and oceanographic processes all of which result in a selective sorting of the sediments. The observed mineral assemblages of transparent heavy minerals (pyroxene, amphibole, tourmaline, kyanite, garnet, zircon and olivine) are suggestive of their derivation from a heterogeneous provenance comprising of igneous rocks, high grade metamorphic rocks and reworked Kaladgi sediments. The chromite grains appear to have been derived from ultrabasic rocks present in the upper reaches of the Gad River. The inferred reserves of ilmenite, magnetite and chromite are 0.175, 0.395 and 0.032 million tons, respectively.  相似文献   

11.
《International Geology Review》2012,54(14):1706-1727
ABSTRACT

The Tehuitzingo ultramafic body (Acatlán Complex, southern Mexico) is a strongly serpentinized harburgitic body that encloses chromitite bodies and blocks of eclogitic rocks. Hydrous retrograde metamorphism on chromitite bodies resulted in the formation of: i) partly altered chromite characterized by unaltered cores surrounded by Fe2+-rich and Al-depleted porous chromite containing chlorite; ii) porous chromite corresponding to a chromite that was entirely transformed to Fe2+-rich and Al-depleted porous chromite; and iii) zoned chromite formed by modified cores surrounded by Fe3+-rich non-porous chromite and magnetite rims. The content of minor and trace elements (Ga, Ti, Ni, Zn, Co, Mn, V, Sc) in the cores of partly altered chromite preserves the magmatic fingerprint of back-arc-bearing chromitites, while the cores of zoned chromite are enriched in Zn, Co and Mn but depleted in Ga, Ti, Ni and Sc, and display a metamorphic signature. P-T pseudosections performed in the system CrMFASH allow us to constrain the temperature of formation of Fe2+-rich chromite by reaction of magmatic chromite with olivine between 584 and 449 °C; while the new thermodynamic calculations performed in the FMASH system shows that the Fe3+-rich non-porous chromite and magnetite rims in zoned chromites were formed at lower temperatures (i.e. 270–340 ºC and < 20 kbar). Temperatures of alteration obtained using our new thermodynamic model are in agreement with the qualitative estimation that use minor and trace elements in Fe2+-rich chromite (i.e. 560–700 ºC). These temperatures are more restricted than those estimated for chlorite hosted in partly altered (193–481 ºC) and porous chromite (158–255 ºC), and those reported in host serpentinite and associated eclogitic rocks (210–399 ºC). A comparison of P-T conditions estimated by our new thermodynamic models and the distribution of minor and trace elements in the different zones of chromites allow us to infer that the alteration took place during the hydrous retrograde metamorphism, and that the high-pressure metamorphism did not modify the composition of chromites. Thus, the microstructural zoning displayed by chromite grains was formed during the exhumation of a segment of a back-arc-related oceanic lithosphere, at similar temperature conditions than the Tehuitzingo serpentinite.  相似文献   

12.
Dealt with in this paper are some geochemical characteristics of porphyry copper mineralization, especially those observed in intrusive bodies, wall rocks, alteration zones, ores and pyrites. Ore bearing bodies have been correlated with barren ones from such aspects as major and trace elements, copper contents of biotite and pyrite, and distribution pattern of copper. In the mineralized rocks, trace elements show apparent zoning surrounding ore bodies; major and trace elements seem to show some regularities with respect to their variations in the process of alteration, and as a result each alteration zone displays its own peculiar element association. Trace elements in ores can provide information on the genetic types of ore deposits, thus of great help in distinguishing ore types, while those in pyrites may be indicative of the main mineralizing stage, providing clues for distinguishing ore-bearing from barren rocks, and of the extent of denudation of ore bodies.  相似文献   

13.
Summary The Neoproterozoic Bou Azzer ophiolite complex hosts numerous, small lenticular bodies of massive and disseminated chromite. Metallurgical-grade high-Mg and high-Cr spinels (cores with 48–62 wt% Cr2O3) reveal complex alteration patterns of successive Cr and Mn enrichment and loss of Al towards the rims, while the Mg# ratios [(Mg/(Mg + Fe2+)] remain almost constant. Concentration patterns of platinum-group elements are typical for ophiolitic chromitite poor in sulfides, with predominance of the IPGE, variable Rh, and low Pt and Pd. The most abundant platinum-group mineral is Rh-bearing laurite that occurs either included in spinel or in silicate matrix, whereas Os-Ir-Ru alloy is always included in spinel. Laurite inclusions reveal complex intergrowth textures with Rh-Ru-Pt rich alloy, and with Rh-rich sulfide. Most laurites display trends to sulfur-poor compositions leading to local formation of very fine-grained Ru-Os-Ir alloy phases. Ni-Co-Fe sulfides, arsenides and sulfarsenides devoid of PGE are associated with the alteration of chromite. Textural position and chemical composition of the base metal inclusions, as well as comparison of alteration features between chromite and accessory chromian spinel in the Co-Ni-As ores of the Bou Azzer ophiolite indicate a close connection. It is suggested that hydrothermal fluids percolated through the marginal zones of the ophiolite belt during greenschist facies metamorphism and deposited Ni-Co-Fe arsenides, sulfarsenides and minor sulfides as accessories within altered chromitites, and also in structurally favourable zones as Ni-Co-As ores. Author’s address: Dr. Frank Melcher, Federal Institute for Geosciences and Natural Resources, Stilleweg 2, 30655 Hannover, Germany  相似文献   

14.
中国铬铁矿资源的瓶颈状态已持续多年。最近,在西藏罗布莎蛇绿岩地幔橄榄岩的深部勘探发现200万t致密块状铬铁矿床,这是中国近50年来铬铁矿找矿的重大突破,对今后继续寻找同类型的铬铁矿床具有重要指导意义。蛇绿岩地幔橄榄岩中产出的豆荚状铬铁矿床是工业需求铬的重要来源。研究豆荚状铬铁矿的成矿作用和矿体围岩地幔橄榄岩地质特征,建立铬铁矿的成矿模型和找矿标志,是开展寻找同类型矿床的重要保证。随着近些年在豆荚状铬铁矿及围岩地幔橄榄岩中金刚石等深部矿物的不断发现和深入研究,人们对蛇绿岩型铬铁矿的物质来源和形成过程,有了新的认识,提出了铬铁矿的深部成因模式。研究认为深部成因铬铁矿床主要经历了4个阶段:(1)早期俯冲到地幔过渡带(410~660 km)的陆壳和洋壳物质被脱水和肢解,过渡带产生的热和流体促成了地幔的熔融和Cr的释放和汇聚;(2)铬铁矿浆在地幔柱驱动下,运移到过渡带顶部冷凝固结,并有强还原的流体进入,后者携带了深部形成的金刚石、斯石英等高压矿物,进入"塑性—半塑性地幔橄榄岩"中;(3)随着物质向上移动,深度降低,早期超高压相矿物发生相变,如斯石英转变成柯石英,高压相的铬铁矿中出溶成柯石英和单斜辉石;(4)在侵位过程和俯冲带环境下,含水熔体与方辉橄榄岩反应形成了不含超高压矿物的规模相对较小的浸染状铬铁矿及纯橄岩岩壳。进一步研究表明,同处雅鲁藏布江缝合带西段的几个大型地幔橄榄岩岩体与罗布莎岩体可以对比,经历了相同的构造背景和豆荚状铬铁矿的成矿作用,存在较大的找矿空间。  相似文献   

15.
郭国林  杨经绥  刘晓东  徐向珍  武勇 《岩石学报》2016,32(12):3673-3684
本文对罗布莎三个矿区的铬铁矿进行了详细的原位PGM研究,发现罗布莎各个矿区的铬铁矿中PGM组合和显微结构不同,暗示PGM能够记录铬铁矿形成与演化过程。罗布莎矿区的PGM显微特征显示铬铁矿结晶于高温、低硫逸度的环境中,可能系岩石/熔体反应和结晶分异双重作用下的产物;康金拉矿区的原位PGM主要为组合型包裹体,有少量产于铬铁矿裂隙之间的贱金属硫化物和合金矿物,为不同来源的熔体混合作用的结果,并暗示铬铁矿成矿后还受到热液流体的改造;香卡山矿区的PGM表明铬铁矿成矿之后遭受到还原性流体的交代作用,铬铁矿中早期结晶出来的硫化物或者铂族矿物被还原改造,形成铁镍矿等次生矿物,保存于铬铁矿粒间或者铬铁矿的裂隙中,这个过程可能与蛇纹石化或者晚期构造流体改造作用有关。罗布莎原位PGM研究表明,PGM矿物贯穿于铬铁矿结晶成矿过程的始终,PGM的矿物及其组合能够记录铬铁矿结晶时母熔体的物理化学条件,甚至还能反映铬铁矿成矿后所经历的后期构造热液事件。因此,结合单矿物分选和原位调查两种方法,查明铬铁矿中PGM的赋存类型及微观结构,对全面理解铬铁矿的成矿过程有重要意义。  相似文献   

16.
An earlier investigation of metasomatic alteration (Curtis and Brown, 1969) is extended to trace element distribution. Most element profiles may be linked simply with diffusive mixing. Between element differentiation is slight, but certain elements are selectively concentrated in particular mineral phases.Trace elements never exhibit the spectacular unmixing shown by some major elements as monomineralic zones develop. Local equilibrium considerations still contribute materially to an understanding of overall behavior.  相似文献   

17.
High-resolution X-ray computed tomography has been carried out on a suite of komatiite samples representing a range of volcanic facies, chromite contents and degrees of alteration and metamorphism, to reveal the wide range of sizes, shapes and degrees of clustering that chromite grains display as a function of cooling history. Dendrites are spectacularly skeletal chromite grains formed during very rapid crystallization of supercooled melt in spinifex zones close to flow tops. At slower cooling rates in the interiors of thick flows, chromite forms predominantly euhedral grains. Large clusters (up to a dozen of grains) are characteristic of liquidus chromite, whereas fine dustings of mostly individual ~20-μm grains form by in situ crystallization from trapped intercumulus liquid. Chromite in coarse-grained olivine cumulates from komatiitic dunite bodies occurs in two forms: as clusters or chains of euhedral crystals, developing into “chicken-wire” texture where chromite is present in supra-cotectic proportions; and as strongly dendritic, semi-poikilitic grains. These dendritic grains are likely to have formed by rapid crescumulate growth from magma that was close to its liquidus temperature but supersaturated with chromite. In some cases, this process seems to have been favoured by nucleation of chromite on the margins of sulphide liquid blebs. This texture is a good evidence for the predominantly cumulus origin of oikocrysts and in situ origin of heteradcumulate textures. Our 3D textural analysis confirms that the morphology of chromite crystals is a distinctive indicator of crystallization environment even in highly altered rocks.  相似文献   

18.
The distinction between Ru in solid solution and Ru-bearing inclusions is essential for the predictive modeling of platinum-group element (PGE) geochemistry in applications such as the lithogeochemical exploration for magmatic sulfide deposits in komatiites. This study investigates the role of chromite in the fractionation of Ru in ultramafic melts by analyzing chromite grains from sulfide-undersaturated komatiites and a komatiitic basalt from the Yilgarn Craton in Western Australia. In situ analysis using laser ablation ICP-MS yields uniform Ru concentrations in chromites both within-grain and on a sample scale, with concentrations between 220 and 540 ppb. All other platinum-group elements are below the detection limit of the laser ablation ICP-MS analysis. Carius tube digestion isotope dilution ICP-MS analysis of chromite concentrates confirms the accuracy of the in-situ method. Time resolved laser ablation ICP-MS analyses have identified the presence of sub-micron Ir-bearing inclusions in some chromite grains from the komatiitic basalt. However, Ru-bearing inclusions have not been recognized in the analyzed chromites and this combined with the in situ data suggests that Ru exists in solid solution in the crystal lattice of chromite. These results show that chromite can control the fractionation and concentration of Ru in ultramafic systems.  相似文献   

19.
The Mupane gold deposit, which is one of the numerous gold occurrences in the Tati Greenstone Belt in the northeastern part of Botswana, consists of four orebodies, namely Tau, Tawana, Kwena, and Tholo deposits. The present research, which focuses on the genesis of the Tau deposit, was based on ore petrography, mineral chemistry of sulfides, and sulfur isotope data. Mineralogical characteristics of the host rocks indicate that banded iron formation at the Tau deposit includes iron oxides (magnetite), carbonates (siderite and ankerite), silicates (chlorite and amphibole), and sulfides (arsenopyrite and pyrrhotite). The deposit features arsenopyrite-rich zones associated with biotite-chlorite veins, which are indicative of the precipitation of arsenopyrite concomitant with potassic alteration. The replacement of magnetite by pyrrhotite in some samples suggests that sulfidation was likely the dominant gold precipitation mechanism because it is considered to have destabilized gold-thiocomplexes in the ore-forming fluids. Based on textural relationships and chemical composition, arsenopyrite is interpreted to reflect two generations. Arsenopyrite 1 is possibly early in origin, sieve textured with abundant inclusions of pyrrhotite. Arsenopyrite 1 was then overgrown by late arsenopyrite 2 with no porous textures and rare inclusions of pyrrhotite. Gold mineralization was initiated by focused fluid flow and sulfidation of the oxide facies banded iron formation, leading to an epigenetic gold mineralization. The mineralogical assemblages, textures, and mineral chemistry data at the Tau gold deposit revealed two-stage gold mineralizations commencing with the deposition of invisible gold in arsenopyrite 1 followed by the later formation of native gold during hydrothermal alteration and post-depositional recrystallization of arsenopyrite 1. Laser ablation inductively coupled plasma mass spectrometric analysis of arsenopyrite from the Tau deposit revealed that the hydrothermal event responsible for the formation of late native gold also affected the distribution of other trace elements within the grains as evidenced by varying trace elements contents in arsenopyrite 1 and arsenopyrite 2. The range of δ34S of gold-bearing assemblages from the Tau deposit is restricted from +1.6 to +3.9‰, which is typical of Archean orogenic gold deposits and indicates that overall reduced hydrothermal conditions prevailed during the gold mineralization process at the Tau deposit. The results from this study suggest that gold mineralization involved multi-processes such as sulfidation, metamorphism, deformation, hydrothermal alteration, and gold remobilization.  相似文献   

20.
La Cabaña peridotite is part of a dismembered ophiolite complex located within the metamorphic basement of the Coastal Cordillera of south-central Chile, and is the only location in Chile were Cr-spinels have been described so far. The La Cabaña peridotite is part of the Western Series unit, which comprises meta-sedimentary rocks, metabasites, and serpentinized ultramafic rocks. This unit has been affected by greenschist-facies metamorphism with reported peak PT conditions of 7.0–9.3 kbar and 380°–420 °C. Within La Cabaña peridotite Cr-spinels are present in two localities: Lavanderos and Centinela Bajo. In Lavanderos, Cr-spinel occurs in small chromitite pods and as accessory/disseminated grains with a porous or spongy texture in serpentinite, whereas in Centinela Bajo Cr-spinel is present as accessory zoned grains in partly serpentinized dunites, and in chromitite blocks. All Cr-spinels display variable degrees of alteration to Fe2+-rich chromite with a variation trend of major elements from chromite to Fe2+-rich chromite similar to those observed in other locations, i.e., an increase in Fe2O3 and FeO, a decrease in Al2O3 and MgO. Cr2O3 content increases from chromite to Fe2+-rich chromite in chromitite pods from Lavanderos and chromitite blocks from Centinela Bajo, but decreases in ferrian chromite zones in accessory grains from Centinela Bajo. The minor element (Ti, V, Zn, Ni) content is mostly low and does not exceed 0.4 wt.%, with the exception of MnO (<0.9 wt.%), which shows a correspondence with increasing degree of alteration. Cr# (Cr/Cr?+?Al) versus Mg# (Mg/Mg?+?Fe2+) and Fe3+/Fe3++Fe2+ versus Mg# plots are used to illustrate the Cr-spinel alteration process. Overall, the Cr-spinels from Lavanderos (chromitite pods and disseminated grains) exhibit Cr# values ranging from 0.6 to 1.0, Mg# (Mg/Mg?+?Fe2+) below 0.5, and (Fe3+/Fe3++Fe2+) <0.4. Cr-spinels from chromitites in Centinela Bajo have Cr# and Mg# values that range from 0.65 to 1.0, and 0.7-0.3, respectively, and (Fe3+/Fe3++Fe2+)?3+/Fe3++Fe2+) ratio is less than 0.4 in chromite cores and Fe2+-rich chromite, and >0.5 in ferrian chromite and Cr-magnetite. Interpretation of the data obtained and Cr-spinel textures indicate that the alteration of Cr-spinel is a progressive process that involves in its initial stages the reaction of chromite with olivine under water-saturated conditions to produce clinochlore and Fe2+-rich chromite. During this stage the chromite can also incorporate Ni, Mn, and/or Zn from the serpentinization fluids. As alteration progresses, Fe2+-rich chromite loses mass resulting in the development of a spongy texture. In a later stage and under more oxidizing conditions Fe3+ is incorporated in chromite/Fe2+-rich chromite shifting its composition to an Fe3+-rich chromite (i.e., ferrian chromite). Depending on the fluid/rock and Cr-spinel/silicate ratios, Cr-magnetite can also form over Fe2+-rich chromite and/or ferrian chromite as a secondary overgrowth. The compositional changes observed in Cr-spinels from La Cabaña reflect the initial stages of alteration under serpentinization conditions. Results from this study show that the alteration of Cr-spinels is dependent on temperature. The degree and extent of alteration (formation of Fe2+-rich and/or ferrian chromite) are controlled by the redox nature of the fluids, the Cr-spinel/silicate and the fluid/rock ratios.  相似文献   

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