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1.
石青硐矿区处于北祁连褶皱带东段,与著名的白银大型矿田组成白银-石青硐铜多金属成矿亚带。文章对石青硐矿床不同类型的含矿围岩及矿石进行了稀土元素特征的对比研究,分析认为:(1)区内含矿围岩的稀土配分模式与白银厂相似,基性岩由板块俯冲环境下地幔楔部分熔融产生,并有地壳混染,酸性岩则为基性岩浆分异并混染了地壳物质的产物,成矿与成岩物质具有一定的继承性和同源性;(2)δEu和δCe特征表明,石英脉型多金属矿石的成矿流体和物质主要来源于高温还原性质的岩浆热液,而浸染型矿石的形成可能与海底热液对流循环成矿作用相关;(3)无矿石英脉与基性岩关系密切,其可能来源于氧化条件下基性岩中的硅质淋滤和再沉淀;(4)无矿石英脉与多金属矿化石英脉的Eu异常明显不同,前者为负Eu异常而后者为正Eu异常,即Eu异常可以作为石英脉含矿性评价的地球化学标志。 相似文献
2.
湘黔汞矿带位于扬子准地台南侧、扬子褶皱带与江南地轴结合部的保靖-铜仁深大断裂的东侧,南起湖南新晃酒店塘,经贵州万山、铜仁大硐喇,至湖南凤凰茶田、向北延至保靖水银厂,全长约150 km、宽5～10 km. 相似文献
3.
茂租铅锌矿床位于扬子地台西南缘,是滇东北矿集区内的一个大型矿床,矿体主要呈似层状产于震旦系灯影组白云岩中;矿石矿物以闪锌矿为主,次为方铅矿;脉石矿物主要为白云石、方解石和萤石。本文对该矿床中与铅锌矿密切共生的团块状白云石、方解石和萤石以及围岩灯影组白云岩的REE地球化学特征和C、O、Sr同位素进行了对比研究。结果表明:团块状白云石和方解石的稀土配分模式、C同位素和Sr同位素比值与围岩灯影组白云岩比较接近,表明形成团块状白云石和方解石的成矿流体主要来源于围岩灯影组白云岩的溶解;但这两种矿物的稀土总量ΣREE高于灯影组白云岩,说明成矿流体除了主要由围岩提供REE外,还有部分其他富含REE流体的加入。萤石则具有LREE亏损和分配曲线相对平缓的稀土配分模式特征,表明萤石形成于成矿的晚阶段,有更多的外部流体的加入。团块状白云石、方解石和萤石表现出明显的Eu正异常,且团块状白云石和方解石的O同位素低于灯影组白云岩,反映了存在较高温度的流体活动,这3种脉石矿物是由高温热液流体形成的。灯影组白云岩和3种脉石矿物都具有明显的Ce负异常,说明成矿流体可能主要来源于地层循环水,继承了围岩的Ce负异常特征。方解石和萤石的Sr同位素比值高于围岩震旦系灯影组白云岩和峨眉山玄武岩,但小于基底岩石昆阳群和会理群,说明成矿流体主要由赋矿围岩等沉积地层中的循环流体与流经了基底岩石的深部流体混合形成。 相似文献
4.
本文采用四极等离子质谱仪(ICP-MS)方法测定了可可塔勒铅锌矿矿物流体包裹体的稀土元素含量。研究表明,成矿流体稀土元素配分模式均为轻稀土富集,Eu具有明显正异常。矿石硫化物流体包裹体稀土特征具有3种稀土配分模式,即平滑右倾型、平坦型、倒“V”字型,矿体下盘围岩的稀土总量明显高于上盘围岩的稀土总量,具有明显的Eu的负异常,成矿流体具有多来源、成矿具有多阶段叠加特点,具有双淋滤模式特征。 相似文献
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近年来,位于扬子板块东南缘的花垣铅锌矿田取得重大找矿突破,杨家寨和大脑坡等一系列大型-超大型铅锌矿的发现,该区新增铅锌资源储量已经超过1000万t,有望成为世界级铅锌资源基地。虽然该矿田地质地球化学研究已经积累了较多成果,但关于铅锌成矿流体的来源及其演化过程研究相对薄弱,制约了花垣矿田的成矿机制深入。本文通过对该矿田不同成矿阶段热液方解石稀土组成研究,并与矿区围岩和不同时代地层对比,探讨矿田内铅锌成矿流体来源及其演化。研究表明,不同成矿阶段的方解石稀土元素及配分模式差异明显,其中成矿早晚2阶段方解石REE与围岩较相似,而主成矿阶段方解石明显富集REE,暗示成矿流体不可能完全由赋矿地层提供,应有来自下伏地层以及基底岩石相对富集REE的流体加入,这种流体可能携带了大量的Pb、Zn成矿物质,为铅锌矿成矿提供了物质来源。此外,成矿早阶段到主成矿阶段,δEu值均小于1,暗示成矿早阶段到主成矿阶段的流体呈现相对还原的特征;而成矿晚阶段方解石的δEu远大于1,表明成矿晚阶段热液流体呈现较氧化特征,总体而言,本区成矿环境在铅锌成矿过程中由相对还原向相对氧化的演化。 相似文献
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吴刚培 《物探化探计算技术》1980,(4)
一、概述驰名中外的湘黔汞矿带,由数十个具有一定层位的层控矿床组成。大硐喇汞矿田位于湘黔汞矿带中段,已知工业矿体皆产于寒武系中统敖溪组第五岩性段(∈_(2a)~5)细粒结晶白云岩中。矿田内各矿床主要受北西西向褶曲控制,多沿褶曲长轴方向展布,并因汞矿在含矿层中产出部位不同,而有“顶部矿”与“中下部矿”之分。含矿层的上覆及下伏岩层泥质含量高于含矿 相似文献
8.
桂北沙子江铀矿床稀土元素地球化学特征 总被引：1，自引：0，他引：1
针对沙子江矿床的区域地层、赋矿围岩、成矿各阶段方解石及铀矿石进行稀土元素地球化学研究发现:各类样品具大体类似的LREE富集及Eu负异常的稀土配分模式,表明它们之间稀土元素特征具有继承性,赋矿花岗岩与区域地层稀土元素特征指示两者具有共同的陆壳沉积物源区;方解石及矿石中稀土元素主要继承了赋矿花岗岩的特征。成矿各阶段方解石Y/Ho值范围狭窄,在28.86~38.22之间,显示它们具共同的源区,且从成矿早阶段经主成矿阶段到成矿晚阶段,Eu负异常趋于强烈,δEu均值由0.34→0.26→0.25,表明成矿流体向相对还原环境演化。铀矿石具最高的稀土元素总量(ΣREE=259.88×10-6~869.31×10-6),且与铀矿石的品位存在正相关关系,暗示稀土元素与铀的迁移具同步性。铀矿石(以原生铀矿物为主)中Ce负异常的形成可能与铀源岩中分散的U(Ⅳ)被活化为在成矿流体中易迁移的U(Ⅵ)的氧化过程相伴;而铀黑的Ce正异常则是由表生作用过程所导致。 相似文献
9.
贵州紫云方解石矿床是在贵州西南部新发现的非金属矿床,方解石矿体呈脉状、透镜状和似层状产出。对紫云火山关、达则等方解石矿床开展同位素地球化学及微量元素、稀土元素研究,结果表明碳、氧同位素显示成矿物质来源于海相碳酸盐岩,成矿流体以富含HCO3-为主,大气水参与成矿,与岩浆作用关系不大。其中达则矿段相对于围岩,成矿物质具有较高的Sr、Zn和Ni含量,稀土元素配分曲线明显区别于围岩,δEu显示正异常等特征,暗示可能有深部流体参与成矿。火山关、打劳等其他矿段,矿体和围岩具有相似的稀土配分模式和∑REE变化规律,表明成矿物质来源于碳酸盐岩围岩。通过区域成矿作用比较,认为成矿时代可能属于印支—燕山期。 相似文献
10.
《华南地质与矿产》2017,(3)
本文利用电感耦合等离子体质谱(ICP-MS)分析了湖南花垣地区铅锌矿床中闪锌矿、方铅矿、黄铁矿以及围岩灰岩中的稀土元素含量,并对成矿物质及成矿流体来源进行了探讨。测试结果表明:花垣地区铅锌矿床矿石硫化物的稀土总量较低,平均值为0.16×10-6,明显低于围岩灰岩的稀土元素总量平均值5.75×10-6。具有高的ΣLREE/ΣHREE比值,轻重稀土分馏明显,轻稀土富集,重稀土亏损,稀土配分曲线均为右倾型。三种矿石硫化物样品多表现出正Eu异常,弱正Ce异常的特点,围岩灰岩则存在中等程度的负Eu异常和负Ce异常。矿石硫化物的Y/Ho值主要介于11~23,低于围岩灰岩的Y/Ho值26~39。两者稀土元素组成具有较大的差异性,反映了矿石硫化物与赋矿围岩灰岩之间的非同源性,推断该区含矿层并不是成矿物质的主要来源,成矿物质应来源于古老基底地层和下伏地层牛蹄塘组,成矿流体来源为具有海水混合的还原性热液流体。 相似文献
11.
Most sulfide-rich magmatic Ni-Cu-(PGE) deposits form in dynamic magmatic systems by partial melting S-bearing wall rocks with variable degrees of assimilation of miscible silicate and volatile components, and generation of barren to weakly-mineralized immiscible Fe sulfide xenomelts into which Ni-Cu-Co-PGE partition from the magma. Some exceptionally-thick magmatic Cr deposits may form by partial melting oxide-bearing wall rocks with variable degrees of assimilation of the miscible silicate and volatile components, and generation of barren Fe ± Ti oxide xenocrysts into which Cr-Mg-V ± Ti partition from the magma. The products of these processes are variably preserved as skarns, residues, xenoliths, xenocrysts, xenomelts, and xenovolatiles, which play important to critical roles in ore genesis, transport, localization, and/or modification. Incorporation of barren xenoliths/autoliths may induce small amounts of sulfide/chromite to segregate, but incorporation of sulfide xenomelts or oxide xenocrysts with dynamic upgrading of metal tenors (PGE > Cu > Ni > Co and Cr > V > Ti, respectively) is required to make significant ore deposits. Silicate xenomelts are only rarely preserved, but will be variably depleted in chalcophile and ferrous metals. Less dense felsic xenoliths may aid upward sulfide transport by increasing the effective viscosity and decreasing the bulk density of the magma. Denser mafic or metamorphosed xenoliths may also increase the effective viscosity of the magma, but may aid downward sulfide transport by increasing the bulk density of the magma. Sulfide wets olivine, so olivine xenocrysts may act as filter beds to collect advected finely dispersed sulfide droplets, but other silicates and xenoliths may not be wetted by sulfides. Xenovolatiles may retard settling of – or in some cases float – dense sulfide droplets. Reactions of sulfide melts with felsic country rocks may generate Fe-rich skarns that may allow sulfide melts to fractionate to more extreme Cu-Ni-rich compositions. Xenoliths, xenocrysts, xenomelts, and xenovolatiles are more likely to be preserved in cooler basaltic magmas than in hotter komatiitic magmas, and are more likely to be preserved in less dynamic (less turbulent) systems/domain/phases than in more dynamic (more turbulent) systems/domains/phases. Massive to semi-massive Ni-Cu-PGE and Cr mineralization and xenoliths are often localized within footwall embayments, dilations/jogs in dikes, throats of magma conduits, and the horizontal segments of dike-chonolith and dike-sill complexes, which represent fluid dynamic traps for both ascending and descending sulfides/oxides. If skarns, residues, xenoliths, xenocrysts, xenomelts, and/or xenovolatiles are present, they provide important constraints on ore genesis and they are valuable exploration indicators, but they must be included in elemental and isotopic mass balance calculations. 相似文献
12.
《Chemical Geology》2007,236(1-2):13-26
We examined the coprecipitation behavior of Ti, Mo, Sn and Sb in Ca–Al–Mg fluorides under two different fluoride forming conditions: at < 70 °C in an ultrasonic bath (denoted as the ultrasonic method) and at 245 °C using a Teflon bomb (denoted as the bomb method). In the ultrasonic method, small amounts of Ti, Mo and Sn coprecipitation were observed with 100% Ca and 100% Mg fluorides. No coprecipitation of Ti, Mo, Sn and Sb in Ca–Al–Mg fluorides occurred when the sample was decomposed by the bomb method except for 100% Ca fluoride. Based on our coprecipitation observations, we have developed a simultaneous determination method for B, Ti, Zr, Nb, Mo, Sn, Sb, Hf and Ta by Q-pole type ICP-MS (ICP-QMS) and sector field type ICP-MS (ICP-SFMS). 9–50 mg of samples with Zr–Mo–Sn–Sb–Hf spikes were decomposed by HF using the bomb method and the ultrasonic method with B spike. The sample was then evaporated and re-dissolved into 0.5 mol l− 1 HF, followed by the removal of fluorides by centrifuging. B, Zr, Mo, Sn, Sb and Hf were measured by ID method. Nb and Ta were measured by the ID-internal standardization method, based on Nb/Mo and Ta/Mo ratios using ICP-QMS, for which pseudo-FI was developed and applied. When 100% recovery yields of Zr and Hf are expected, Nb/Zr and Ta/Hf ratios may also be used. Ti was determined by the ID-internal standardization method, based on the Ti/Nb ratio from ICP-SFMS. Only 0.053 ml sample solution was required for measurement of all 9 elements. Dilution factors of ≤ 340 were aspirated without matrix effects. To demonstrate the applicability of our method, 4 carbonaceous chondrites (Ivuna, Orgueil, Cold Bokkeveld and Allende) as well as GSJ and USGS silicate reference materials of basalts, andesites and peridotites were analyzed. Our analytical results are consistent with previous studies, and the mean reproducibility of each element is 1.0–4.6% for basalts and andesites, and 6.7–11% for peridotites except for TiO2. 相似文献
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15.
Hirokazu Fujimaki 《Contributions to Mineralogy and Petrology》1986,94(1):42-45
Concentration ratios of Hf, Zr, and REE between zircon, apatite, and liquid were determined for three igneous compositions: two andesites and a diorite. The concentration ratios of these elements between zircon and corresponding liquid can approximate the partition coefficient. Although the concentration ratios between apatite and andesite groundmass can be considered as partition coefficients, those for the apatite in the diorite may deviate from the partition coefficients. The HREE partition coefficients between zircon and liquid are very large (100 for Er to 500 for Lu), and the Hf partition coefficient is even larger. The REE partition coefficients between apatite and liquid are convex upward, and large (D=10–100), whereas the Hf and Zr partition coefficients are less than 1. The large differences between partition coefficients of Lu and Hf for zircon-liquid and for apatite-liquid are confirmed. These partition coefficients are useful for petrogenetic models involving zircon and apatite. 相似文献
16.
针对兖州煤田下组煤深部开采受奥灰高承压水威胁以及当地大型煤化工企业生产用水量大的现状,在已进行的水文地质勘探及放水试验基础上,评价奥灰富水性,并采用有限差分法进行奥灰疏水降压数值模拟研究,提出水煤共采观点。研究结果表明:兖州煤田深部奥灰水压高,合理布置水煤共采孔,可以实现奥灰水位的有效疏降,疏降中心区水位最大降深可达110 m,突水系数显著下降,提高了下组煤开采的安全性;同时可提供煤化工43200 m3/d的供水量,能达到可持续的、水资源保护性的供水效果,实现下组煤的水煤共采。 相似文献
17.
The distribution of Cu, Co, As and Fe was studied downstream from mines and deposits in the Idaho Cobalt Belt (ICB), the largest Co resource in the USA. To evaluate potential contamination in ecosystems in the ICB, mine waste, stream sediment, soil, and water were collected and analyzed for Cu, Co, As and Fe in this area. Concentrations of Cu in mine waste and stream sediment collected proximal to mines in the ICB ranged from 390 to 19,000 μg/g, exceeding the USEPA target clean-up level and the probable effect concentration (PEC) for Cu of 149 μg/g in sediment; PEC is the concentration above which harmful effects are likely in sediment dwelling organisms. In addition concentrations of Cu in mine runoff and stream water collected proximal to mines were highly elevated in the ICB and exceeded the USEPA chronic criterion for aquatic organisms of 6.3 μg/L (at a water hardness of 50 mg/L) and an LC50 concentration for rainbow trout of 14 μg/L for Cu in water. Concentrations of Co in mine waste and stream sediment collected proximal to mines varied from 14 to 7400 μg/g and were highly elevated above regional background concentrations, and generally exceeded the USEPA target clean-up level of 80 μg/g for Co in sediment. Concentrations of Co in water were as high as in 75,000 μg/L in the ICB, exceeding an LC50 of 346 μg/L for rainbow trout for Co in water by as much as two orders of magnitude, likely indicating an adverse effect on trout. Mine waste and stream sediment collected in the ICB also contained highly elevated As concentrations that varied from 26 to 17,000 μg/g, most of which exceeded the PEC of 33 μg/g and the USEPA target clean-up level of 35 μg/g for As in sediment. Conversely, most water samples had As concentrations that were below the 150 μg/L chronic criterion for protection of aquatic organisms and the USEPA target clean-up level of 14 μg/L. There is abundant Fe oxide in streams in the ICB and several samples of mine runoff and stream water exceeded the chronic criterion for protection of aquatic organisms of 1000 μg/L for Fe. There has been extensive remediation of mined areas in the ICB, but because some mine waste remaining in the area contains highly elevated Cu, Co, As and Fe, inhalation or ingestion of mine waste particulates may lead to human exposure to these elements. 相似文献
18.
E. M. Prasolov S. A. Sergeev B. V. Belyatsky E. S. Bogomolov K. A. Gruzdov I. N. Kapitonov R. Sh. Krymsky V. O. Khalenev 《Geochemistry International》2018,56(1):46-64
This paper reports the first results of a study of 11 isotope systems (3He/4He, 40Ar/36Ar, 34S/32S, 65Cu/63Cu, 62Ni/60Ni, 87Sr/86Sr, 143Nd/144Nd, 206–208Pb/204Pb, Hf–Nd, U–Pb, and Re–Os) in the rocks and ores of the Cu–Ni–PGE deposits of the Norilsk ore district. Almost all the results were obtained at the Center of Isotopic Research of the Karpinskii All-Russia Research Institute of Geology. The use of a number of independent genetic isotopic signatures and comprehensive isotopic knowledge provided a methodic basis for the interpretation of approximately 5000 isotopic analyses of various elements. The presence of materials from two sources, crust and mantle, was detected in the composition of the rocks and ores. The contribution of the crustal source is especially significant in the paleofluids (gas–liquid microinclusions) of the ore-forming medium. Crustal solutions were probably a transport medium during ore formation. Air argon is dominant in the ores, which indicates a connection between the paleofluids and the atmosphere. This suggests intense groundwater circulation during the crystallization of ore minerals. The age of the rocks and ores of the Norilsk deposits was determined. The stage of orebody formation is restricted to a narrow age interval of 250 ± 10 Ma. An isotopic criterion was proposed for the ore-bearing potential of mafic intrusions in the Norilsk–Taimyr region. It includes several interrelated isotopic ratios of various elements: He, Ar, S, and others. 相似文献
19.
Todd Dunn 《Contributions to Mineralogy and Petrology》1987,96(4):476-484
The crystal/liquid partition coefficients of Lu, Hf, Ti, Mn and Ca have been measured between olivine, clinopyroxene and basaltic melt. The Ti, Mn, and Ca partition coefficients were determined at natural abundance levels. The Lu and Hf partition coefficients were determined at doping levels ranging from 0.5 to 1.5 wt% “trace element” as oxide in order to allow analysis by electron microprobe. Olivine/liquid partition coefficients for Lu, Hf, Ti, Mn, and Ca were determined at 1 bar and temperatures from 1150 to 1177° C. Clinopyroxene/liquid partition coefficients were determined for Lu, Hf, Ti, and Mn at pressures of 10, 15, and 20 kbars and temperatures from 1250 to 1290° C. The olivine/liquid partition coefficients of Hf, Lu, Ti, and Ca are small. D(Hf-ol) is zero within the analytical uncertainty. Both D(Lu-ol) and D(Mn-ol) decrease with increasing temperature, but D(Ti-ol) and D(Ca-ol) are constant over the narrow temperature range studied. The partition coefficient results are summarized below.
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20.
Stratiform quartz-sulphide lodes in Ingladhal occur in a typical Precambrian green-stone-belt environment comprising metabasalts, tuff, chert and cherty iron-sulphide formation. Unusually high cobalt contents of metavolcanics and of sulphide minerals in orebodies suggest a consanguinity between ores and rocks. 90% of total nickel, 70% of total cobalt but only 30% of total copper in rocks occur in silicate phases and thus indicate an early separation of copper from cobalt and nickel. Unusually high non-sulphide copper in barren bedded cherts implies availability of Cu-rich solution prior to their lithification. Pyrite in sediments, in volcanics, and in orebodies is characterized by a distinctive pattern of Co-Ni distribution in each case. Partitioning of Co and Ni between coexisting sulphide pairs is complex, but gross equilibrium is indicated. Very high trace metal content of orebody pyrite sharply contrasts with very low such values in pyrite from adjacent sediments and points to a higher temperature of formation of orebodies. 相似文献
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