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1.
海南省新村钼矿床LA-ICP-MS锆石U-Pb和辉钼矿Re-Os年龄及其地质意义 总被引：1，自引：1，他引：0
新村钼矿床是海南省近年来发现的具中型规模的钼矿床。文章对赋矿二长花岗岩进行LA-ICP-MS锆石U-Pb同位素测年,获得~(206)Pb/~(238)U年龄加权平均值为(102.0±1.5)Ma(MSWD=2.3);对辉钼矿进行Re-Os同位素定年,获得5件样品的模式年龄范围为(97.29±1.43)Ma~(98.52±1.55)Ma,加权平均年龄为(97.84±0.64)Ma,等时线年龄为(98.90±3.40)Ma,成岩年龄与成矿年龄在误差范围内一致。辉钼矿的Re含量和锆石Hf同位素特征指示新村钼矿的成岩成矿物质来自于壳幔混源。新村钼矿床的成岩成矿年龄与海南岛最重要的钼成矿期(95~105 Ma)一致,属中国东部早白垩世晚期—晚白垩世早期钼成矿事件的一部分,与该时期岩石圈大规模拉伸减薄、软流圈上涌及强烈壳-幔作用密切相关。 相似文献
2.
内蒙古丰镇市泉子沟斑岩钼矿床成岩成矿年代学及其地质意义 总被引：1，自引：0，他引：1
泉子沟斑岩钼矿床位于内蒙古丰镇市,地处华北克拉通北缘内蒙古台隆凉城断隆内。矿区出露一套燕山期花岗质杂岩体——红娘山杂岩体,主要由中粗粒花岗岩、似斑状花岗岩和石英斑岩组成,钼矿体主要赋存于似斑状花岗岩中。文章在详细的野外地质调查基础上,对泉子沟矿床的成岩成矿时代进行了详细研究,并探讨了地质意义。5件辉钼矿样品的Re-Os模式年龄介于(158.8±2.2)Ma~(161.5±2.2)Ma之间,其加权平均值为(159.8±1.0)Ma(MSWD=0.92),等时线年龄为(161.7±3.1)Ma(MSWD=1.40)。红娘山杂岩体LA-ICP-MS锆石U-Pb年龄分别为:中粗粒花岗岩结晶年龄为(173±1)Ma(MSWD=0.88),似斑状花岗岩侵位年龄为(162±1)Ma(MSWD=0.40),石英斑岩结晶年龄为(160±2)Ma(MSWD=1.90)。辉钼矿Re-Os和锆石U-Pb定年结果表明,泉子沟钼矿床形成于晚侏罗世早期,成矿与似斑状花岗岩关系密切。泉子沟钼矿床的辉钼矿w(Re)介于16.49×10~(-6)~32.87×10~(-6),暗示成矿物质主要来自下地壳。 相似文献
3.
赣西北大雾塘钨矿区地质特征及Re-Os同位素年代学研究 总被引：2，自引：1，他引：1
通过对大湖塘钨矿田的大雾塘钨矿区辉钼矿Re-Os同位素年代学的研究,测得辉钼矿的w(Re)为0.3368×10~(-6)~8.256×10~(-6),获得的5个模式年龄比较一致,介于(136.6±2.2)Ma~(138.4±2.4)Ma,加权平均年龄为(137.7±2.7)Ma(MSWD=0.07)。将5个模式年龄进行等时线年龄计算,获得一条相关性较好的~(187)Re-~(187)Os等时线,计算得到辉钼矿Re-Os等时线年龄为(137.9±2.0)Ma(MSWD=0.20),与加权平均年龄一致,可代表辉钼矿的形成年龄。结合石门寺和狮尾洞矿区典型矿床地质、地球化学特征和成岩作用时空关系,认为大雾塘矿床的形成是大湖塘钨矿田的第二期次(140 Ma)大规模成矿作用的产物,2期成矿作用可能是大湖塘钨矿田巨量成矿元素堆积的重要原因之一。 相似文献
4.
《矿物岩石》2017,(2)
哈陇休玛钼(钨)矿床位于东昆仑东段地区,矿床成因为斑岩型,花岗闪长斑岩与成矿关系密切。应用锆石LA-ICP-MS U-Pb法和Re-Os同位素测年法对1件花岗闪长斑岩样品和4件辉钼矿样品进行精确定年。结果表明:成矿花岗闪长斑岩体的形成年龄为(224.68±0.88)Ma(MSWD=0.85);4件辉钼矿样品和1件重复样品的辉钼矿Re-Os等时线年龄为(223.5±1.3)Ma(MSWD=0.66),模式年龄的加权平均值分别为(224.0±1.5)Ma(MSWD=1.8),等时线年龄与模式年龄加权平均值在误差范围内一致。等时线年龄代表了辉钼矿的结晶时间,证实矿区成岩成矿时代晚三叠世,稍晚于东昆仑西段地区钼成矿时代(钼矿主成矿期为中三叠世)。本区辉钼矿w(Re)为4.37×10~(-6)~38.26×10~(-6),平均16.55×10~(-6)与壳幔混源的辉钼矿w(Re)相近(n×10~(-5)),成矿物质来源可能为壳幔混合源,与整个东昆仑造山带晚三叠世强烈壳-幔相互作用大背景相一致。 相似文献
5.
岗讲铜钼矿床是西藏冈底斯成矿带中段典型的斑岩型矿床,岗讲矿床成岩成矿时代、岩浆演化过程及其与成岩成矿关系尚不明确,利用LA-ICP-MS锆石U-Pb定年方法对岗讲矿区主要岩体二长花岗斑岩、花岗闪长斑岩和英云闪长玢岩成岩时代进行研究,获得锆石U-Pb年龄加权平均值分别为16.6±0.3 Ma (MSWD=0.94,n=10)、16.1±0.2 Ma (MSWD=1.07,n=12)、14.4±0.4 Ma (MSWD=1.12,n=7);同时采用辉钼矿Re-Os同位素测年方法首次对岗讲矿床石英硫化物脉中的辉钼矿进行定年,获得12件辉钼矿Re-Os同位素模式年龄集中于13.24±0.20 Ma~13.55±0.22 Ma,加权平均年龄为13.4±0.1 Ma (MSWD=0.65),等时线年龄为13.6±1.6 Ma (MSWD=1.2).结果表明:(1) 岗讲矿区复式岩体侵入序列为含巨斑黑云二长花岗岩-二长花岗斑岩-花岗闪长斑岩-流纹斑岩 (深部定名为英云闪长玢岩),成岩时限为16.6~14.4 Ma,成矿时代为13.4 Ma左右,成岩成矿是一个连续的岩浆演化过程;(2) 辉钼矿中Re含量为155.4~171.1 μg/g,均值为162.9 μg/g,指示其成矿物质中有幔源成分的加入;(3) 矿床产出于中新世印度-亚洲大陆碰撞后伸展构造环境. 相似文献
6.
内蒙古鸡冠山钼矿流纹斑岩的成岩年龄及地质意义 总被引：1，自引：0，他引：1
内蒙古鸡冠山钼矿床是近年来发现的一个大型斑岩型钼矿床,位于华北克拉通北缘、西拉沐沦钼矿带的中段,产出于一破火山机构的NW侧。矿床矿石矿物辉钼矿Re-Os同位素等时线法测得成矿年龄为151.1±1.3Ma,为晚侏罗世成矿。本文通过SIMS锆石U-Pb年龄法,测定流纹斑岩成岩年龄为148.5±3.3Ma(U-Pb等时线年龄,2σ,MSWD=2.2),为晚侏罗世成岩。该成岩年龄与成矿年龄在误差范围内一致,说明与流纹斑岩有关的岩浆活动可能形成成矿的母岩浆,成岩与成矿近乎同时发生。 相似文献
7.
报道了季德屯、石马洞大型钼矿床地质特征,并对季德屯及石马洞钼矿辉钼矿样品分别进行了Re--Os同位素分析。所获季德屯大型钼矿床辉钼矿的模式年龄值为(168.79±0.42~169.91±0.47)Ma,加权平均年龄为169.31 Ma,等时线年龄为(169.1±1.8)Ma(MSWD=7);石马洞大型钼矿床辉钼矿的模式年龄值为(164.85±1.46~166.21±0.90)Ma,加权平均年龄为165.66 Ma,等时线年龄为(169.3±1.9)Ma(MSWD=1.3)。这些年龄说明两个矿床成矿年龄均为中侏罗世,与大黑山等钼矿成矿年龄基本一致。结合区域上已有的研究成果,认为吉林省中东部钼矿成岩成矿作用主要集中在早—中侏罗世。通过区域构造演化和区域钼矿矿床特征及成岩成矿年龄的分析,认为吉林省中东部大规模钼矿的成矿与太平洋板块的俯冲作用的联系更为密切。 相似文献
8.
内蒙古查干敖包钼矿是宝音图钼矿区矿床之一,为狼山北段发现的斑岩白云母石英脉型钼矿,成矿岩体主要为钾长花岗岩、细晶花岗岩和花岗斑岩,岩体锆石U-Pb平均年龄为(253.5±3.3)Ma。本次研究测得查干敖包辉钼矿的187Re-187Os等时线年龄为(239.2±5.8)Ma,与成矿岩体时代相差约13 Ma,反映钼矿床的形成经历了较长的成岩成矿演化历史。查干敖包钼矿床具有斑岩矿床特点,矿床产于成矿岩体内接触带,但是矿化形成于白云母石英脉中,主要与白云母热液矿物有关,因此是一种特殊的斑岩型钼矿床。 相似文献
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10.
江西省都昌县阳储岭钨钼矿床位于江南造山带东段,为准确厘定阳储岭钨钼矿床的成岩成矿时代,本次在详实的野外地质调查基础上,对阳储岭成矿花岗闪长斑进行锆石U-Pb定年工作,同时开展辉钼矿Re-Os同位素定年研究。LA-ICP-MS锆石U-Pb年龄为（145.08±0.35）Ma（MSWD=0.51,n=7）;辉钼矿Re-Os模式年龄为（143.3±2.0）Ma~（145.5±2.2）Ma,等时线年龄为（145.4±1.0）Ma。阳储岭成矿花岗闪长斑岩锆石U-Pb年龄与辉钼矿Re-Os等时线年龄基本一致,表明阳储岭钨钼矿床成岩成矿时代约为145 Ma。辉钼矿中Re含量为16.62×10-6~87.76×10-6,平均值为44.68×10-6,与壳幔混源岩浆热液矿床中Re的含量相似,指示阳储岭钨钼矿床成矿物质来源于壳幔混源。 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.
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
17.
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
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.
| T°C 相似文献
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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