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1.
四川大渡河金矿田位于扬子地台西缘金成矿带北段,受大渡河剪切带控制。本文以该矿田黄金坪、白金台子、黑金台子金矿为例,根据对黄铁矿流体包裹体氦氩同位素、黄铁矿硫同位素以及与黄铁矿共生的石英流体包裹体的氢氧同位素组成测定,讨论了大渡河金矿田成矿流体的来源。结果显示,该金矿田黄铁矿流体包裹体中的~3He/~4He变化较小,为0.16～0.86Ra,而~(40)Ar/~(36)Ar的变化较大,为298～3288;而黄铁矿δ~(34)S同位素变化范围较窄,一般为0.7‰～4.2‰,集中于2.5‰～3‰,显示硫地幔来源的特点;石英流体包裹体的氢、氧同位素分别为-2.6‰～ 3.64‰和-39.13‰～-108.23‰,说明成矿流体为岩浆水和大气降水的混合流体。本文认为大渡河金矿田成矿流体是地幔流体与地壳流体的混合作用的结果,而以地壳流体占主导地位。其中,地幔流体为与下伏隐伏岩体有关的岩浆水,而地壳流体端元则是含有一定放射成因Ar的大气降水,并且温度小于200℃。 相似文献
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新疆准噶尔地区金矿床成矿流体稀土元素地球化学特征 总被引：11，自引：0，他引：11
新疆准噶尔地区出现大量不同类型金矿床，为了探讨它们的成因，为金矿床的找矿勘探提供依据。笔者进行了哈图、包谷图、阔尔真阔腊、科克萨依等金矿床包裹体流体中稀土元素及同位素等研究。结果表明，尽管它们成矿形式不同，规模不等，但它们的金均主要来自深源，并有地层物质参与。其中哈图金矿石英脉型矿体与蚀变岩型矿体是两种不同来源的流体叠加成矿，石英脉型矿体主要与哈图岩体岩浆流体关系密切，蚀变岩型矿体与深源流体有关。包谷图、阔尔真阔腊金矿矿、科克萨依金矿成矿流体主要来源于深源，成矿过程中受到浅成流体的综合影响。矿物包裹体流体的稀土元素特征主要反映了原始成矿流体来源，矿物的稀土元素特征可能较多地体现了矿床特有的后期地质作用，这在今后研究中将进一步探讨。 相似文献
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甘肃阳山金矿流体包裹体地球化学和矿床成因类型 总被引：16，自引：19，他引：16
西秦岭造山带内的甘肃阳山金矿是我国最新发现的规模最大的金矿床。矿床受 EW 韧脆性剪切带控制,赋矿围岩为泥盆系碳质碳酸盐-千枚岩-板岩和侵入其中的花岗斑岩脉。流体成矿过程包括:形成石英-绢云母-黄铁矿组合的早阶段,形成石英-黄铁矿-毒砂和石英-毒砂-黄铁矿以及石英-碳酸盐-辉锑矿-自然金组合的主成矿阶段,形成碳酸盐-石英网脉的晚阶段。早阶段流体包裹体以含 CO_2包裹体为主,CO_2含量为7.3%～21.5mol%,均一温度集中于270℃～300℃,盐度<3wt.%NaCl eqv;主阶段发育纯 CO_2包襄体、水溶液包裹体和少量含 CO_2包裹体,均一温度集中于210℃～270℃,盐度集中在<2 wt.%NaCl eqv 和3～5 wt.%NaCl eqv 两个范围;晚阶段只发育水溶液包裹体,均一温度集中在160℃～210℃,盐度<3 wt.%NaCl eqv。主阶段流体包裹体类型的多样性、相似的均一温度和流体盐度的双峰特征均指示流体沸腾现象的存在,其流体包裹体捕获温度为210℃～375℃,压力为85～222MPa;赋矿断层的阀门式活动导致主阶段流体系统交替于静岩和静水压力之间,成矿深度为8.5km 左右,成矿流体系统发育在早侏罗世大陆碰撞造山过程。矿床地质特征类似于卡林型金矿。但赋存于蚀变花岗斑岩中矿体既非造山型,也不同于卡林型,成矿流体具造山型矿床特征。因此,阳山金矿可能代表一种新的金矿类型,建议称为"阳山型金矿"。 相似文献
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胶东乳山脉状金矿床成矿流体性质与演化 总被引：10，自引：12，他引：10
位于胶东牟平-乳山金矿带中部的乳山金矿(原称金青顶金矿)是目前我国单脉金储量最大的矿床,金主要产于黄铁矿和多金属硫化物石英脉/细脉中。流体包裹体研究表明,乳山金矿不同蚀变带岩石和各成矿阶段金矿石中的流体包裹体有两种类型:CO_2～H_2O 包裹体和水溶液包裹体。钾长石化蚀变岩、黄铁绢英岩和弱蚀变花岗岩的石英中含有丰富的 CO_2-H_2O 包裹体,而黄铁矿石英脉和多金属硫化物石英脉中 CO_2-H_2O 包裹体数量逐渐减少,以富水的 CO_2-H_2O 两相包裹体和水溶液包裹体为主。显微测温结果显示,弱蚀变花岗岩、钾长石化岩石和黄铁绢英岩石英中的 CO_2-H_2O 包裹体的均一温度范围为236～377℃;而黄铁矿和多金属硫化物石英包裹体的均一温度为170～324℃。成矿早期流体为富含挥发份(X_(CO_2)高达0.53)、中低盐度(3.33～10.48 wt% NaCl)的流体,到主成矿期逐渐演化为以含较低的 CO_2的富水流体(X_(CO_2)为0.01～0.05) 和水溶液流体,盐度为1.23～12.55Wt% NaCl。金和硫化物(尤其是黄铁矿)紧密共生,说明金主要以金硫络合物形式被搬运,CO_2包裹体的广泛存在则表明其对成矿流体的 pH 变化起着重要的抑制作用。水/岩反应、温度下降和压力降低引起的流体不混溶可能是乳山金矿金沉淀成矿的主要原因。 相似文献
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招-平断裂是胶东招掖金矿带的主要控矿断裂,其上盘金矿床受 NE 向断裂构造控制,赋矿围岩为胶东群变质岩,金矿化以含金硫化物石英脉为主。通过首次对招远灵雀山金矿床富金石英脉石英流体包裹体 Rb-Sr 等时线年龄的测定,获得116±23Ma 成矿年龄。从而说明招-平断裂带上盘金矿大规模成矿期发生于早白垩世的构造体系转折期。对富金石英脉石英流体包裹体同位素特征研究表明。该地区成矿热液均以幔源为主,具有与招掖金矿带其它金矿类似的成矿热液系统。由此可以看出招-平断裂带上盘也具有良好的成矿条件。 相似文献
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云南省富宁县者桑金矿床成矿流体特征 总被引：1，自引：0，他引：1
通过云南者桑金矿床中流体包裹体岩相学、显微测温、稀土元素、氢氧同位素的分析,探讨了成矿流体特征。研究表明:存在液体包裹体、纯液体包裹体、纯气体包裹体和含液体CO2包裹体4种流体包裹体类型;液体包裹体均一温度为83.4~248.2℃,盐度为0.18%~6.45%,密度为0.85~1.0 g/cm3,成矿压力为10.9~59.4 MPa,成矿深度为0.2~2.2 km;各成矿阶段石英及方解石稀土元素特征表明,其成矿物理化学条件为还原环境。δ18OH2O值为-6.1‰~4.9‰;δDV-SMOW值为-40.3‰~-74.8‰,表明成矿流体来源为大气降水,岩矿石有机碳含量达到0.12%~0.45%,金品位与有机质含量呈正相关,黄铁矿及毒砂δ34SV-CDT值为9.2‰~10.2‰,表明者桑金矿床成矿热液中硫化物沉淀所需硫源为围岩中有机质与硫酸盐反应提供的还原硫。成矿热液在下渗过程中混合建造水,受到岩浆烘烤作用及地温梯度影响后再向上循环,金矿化发生在成矿流体的热循环与赋矿围岩的相互作用过程中,并在构造有利部位沉淀富集。 相似文献
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南龙王庙金矿位于华北克拉通北缘,产在清原群表壳岩的北东端.主要容矿岩石为新太古代的磁铁石英岩,控矿构造为葫芦头沟-大荒沟韧性剪切带.矿石以细脉-浸染状构造为主.主要蚀变类型有白云母化、硅化、绿泥石化、碳酸盐化和绿帘石化.对矿区细脉-浸染状矿石石英中的流体包裹体进行了系统的岩相学、显微测温分析.结果显示,矿石石英中存在两个不同阶段的流体包裹体：早阶段形成的包裹体主要为含子矿物的三相包裹体（I）;晚阶段形成的包裹体包括气液两相包裹体（II）、纯CO2包裹体（III）和含CO2三相包裹体（IV）三种类型.流体演化过程为：早阶段的中温、高盐度、中等密度的流体,萃取清原群表壳岩中的Au;晚阶段在剪切带韧性变形向脆性变形转化过程中,流体演化为中温、中低盐度、低密度的特征,Au成矿元素达到饱和,在有利的构造空间沉淀成矿.成矿作用的方式由早期的扩散交代逐渐转变为晚期的充填作用,分别形成细脉-浸染状矿体和含金黄铁矿石英脉型矿体. 相似文献
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鄂西北佘家院银金矿特征及成矿模式 总被引：2，自引：0，他引：2
佘家院银金矿是鄂西地区新发现的一种矿床类型。通过矿区地质调查和有关矿床地球化学研究,论述了矿床的地质特征、成矿时代,以太硫、铅同位素和石英流体包裹体特征,提出了深部热源体导矿、褶－断构造容矿和有利岩石组合赋矿的矿床形成模式。 相似文献
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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
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奥地利安东帕有限公司 《岩矿测试》2009,28(3):306-306
最新的流行病学研究表明,空气中较高浓度的悬浮细颗粒可能对人类的健康有不利的影响。根据该项研究显示,由于心脏病、慢性呼吸问题和肺功能指标恶化而导致死亡率的升高与细尘粒子有关。这些研究结果已经促使欧盟于1999年4月出台了限制空气中二氧化硫、二氧化氮、氧化氮、铅和颗粒物含量的法案(1999/30/EC),对各项指标包括对可吸入PM10颗粒的浓度提出了新的限制性指标。PM10颗粒是指可以通过预分级器分离采集的气体动力学直径小于10μm的细颗粒。目前研究的兴趣重点逐步偏向PM2.5这些更细微颗粒物,PM2.5这种颗粒物对健康有明显的不利影响。在欧盟指令2008/50/EC中,对PM10和PM2.5都提 相似文献
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S. Viswanathan K. Surya Prakash Rao B. Mahabaleswar 《Journal of the Geological Society of India》2013,82(6):621-627
Komatiites are mantle-derived ultramafic volcanic rocks. Komatiites have been discovered in several States of India, notably in Karnataka. Studies on the distribution of trace-elements in the komatiites of India are very few. This paper proposes a simple, accurate, precise, rapid, and non-destructive wavelength-dispersive x-ray fluorescence (WDXRF) spectrometric technique for determining Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th in komatiites, and discusses the accuracy, precision, limits of detection, x-ray spectral-line interferences, inter-element effects, speed, advantages, and limitations of the technique. The accuracy of the technique is excellent (within 3%) for Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Zr, Nb, Ba, Pb, and Th and very good (within 4%) for Y. The precision is also excellent (within 3%) for Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th. The limits of detection are: 1 ppm for Sc and V; 2 ppm for Cr, Co, and Ni; 3 ppm for Cu, Zn, Rb, and Sr; 4 ppm for Y and Zr; 6 ppm for Nb; 10 ppm for Ba; 13 ppm for Pb; and 14 ppm for Th. The time taken for determining Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th in a batch of 24 samples of komatiites, for a replication of four analyses per sample, by one operator, using a manual WDXRF spectrometer, is only 60 hours. 相似文献
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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
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《Applied Geochemistry》2001,16(2):137-159
Five hundred and ninety-eight samples of terrestrial moss (Hylocomium splendens and Pleurozium schreberi) collected from a 188,000 km2 area of the central Barents region (NE Norway, N Finland, NW Russia) were analysed by ICP-AES and ICP-MS. Analytical results for Al, B, Ba, Ca, K, La, Mg, Mn, Na, P, Rb, Si, Sr, Th, U and Y concentrations are reported here. Graphical methods of data analysis, such as geochemical maps, cumulative frequency diagrams, boxplots and scatterplots, are used to interpret the origin of the patterns for these elements. None of the elements reported here are emitted in significant amounts from the smelting industry on the Kola Peninsula. Despite the conventional view that moss chemistry reflects atmospheric element input, the nature of the underlying mineral substrate (regolith or bedrock) is found to have a considerable influence on moss composition for several elements. This influence of the chemistry of the mineral substrate can take place in a variety of ways. (1) It can be completely natural, reflecting the ability of higher plants to take up elements from deep soil horizons and shed them with litterfall onto the surface. (2) It can result from naturally increased soil dust input where vegetation is scarce due to harsh climatic conditions for instance. Alternatively, substrate influence can be enhanced by human activity, such as open-cast mining, creation of ‘technogenic deserts’, or handling, transport and storage of ore and ore products, all of which magnify the natural elemental flux from bedrock to ground vegetation. Seaspray is another natural process affecting moss composition in the area (Mg, Na), and this is most visible in the Norwegian part of the study area. Presence or absence of some plant species, e.g., lichens, seems to influence moss chemistry. This is shown by the low concentrations of B or K in moss on the Finnish and Norwegian side of the (fenced) border with Russia, contrasting with high concentrations on the other side (intensive reindeer husbandry west of the border has selectively depleted the lichen population). 相似文献
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Mercury,arsenic, antimony,and selenium contents of sediment from the Kuskokwim River,Bethel, Alaska,USA 总被引：1，自引：0，他引：1
The Kuskokwim River at Bethel, Alaska, drains a major mercury-antimony metallogenic province in its upper reaches and tributaries. Bethel (population 4000) is situated on the Kuskokwim floodplain and also draws its water supply from wells located in river-deposited sediment. A boring through overbank and floodplain sediment has provided material to establish a baseline datum for sediment-hosted heavy metals. Mercury (total), arsenic, antimony, and selenium contents were determined; aluminum was also determined and used as normalizing factor. The contents of the heavy metals were relatively constant with depth and do not reflect any potential enrichment from upstream contaminant sources. 相似文献
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《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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S. M. Moosavirad J. Rasouli M. R. Janardhana M. R. Moghadam M. Shankara 《Arabian Journal of Geosciences》2013,6(10):3623-3634
This paper discusses the result of the detailed investigations carried out on the coal characteristics, including coal petrography and its geochemistry of the Pabedana region. A total of 16 samples were collected from four coal seams d2, d4, d5, and d6 of the Pabedana underground mine which is located in the central part of the Central-East Iranian Microcontinent. These samples were reduced to four samples through composite sampling of each seam and were analyzed for their petrographic, mineralogical, and geochemical compositions. Proximate analysis data of the Pabedana coals indicate no major variations in the moisture, ash, volatile matter, and fixed carbon contents in the coals of different seams. Based on sulfur content, the Pabedana coals may be classified as low-sulfur coals. The low-sulfur contents in the Pabedana coal and relatively low proportion of pyritic sulfur suggest a possible fresh water environment during the deposition of the peat of the Pabedana coal. X-ray diffraction and petrographic analyses indicate the presence of pyrite in coal samples. The Pabedana coals have been classified as a high volatile, bituminous coal in accordance with the vitrinite reflectance values (58.75–74.32 %) and other rank parameters (carbon, calorific value, and volatile matter content). The maceral analysis and reflectance study suggest that the coals in all the four seams are of good quality with low maceral matter association. Mineralogical investigations indicate that the inorganic fraction in the Pabedana coal samples is dominated by carbonates; thus, constituting the major inorganic fraction of the coal samples. Illite, kaolinite, muscovite, quartz, feldspar, apatite, and hematite occur as minor or trace phases. The variation in major elements content is relatively narrow between different coal seams. Elements Sc,, Zr, Ga, Ge, La, As, W, Ce, Sb, Nb, Th, Pb, Se, Tl, Bi, Hg, Re, Li, Zn, Mo, and Ba show varying negative correlation with ash yield. These elements possibly have an organic affinity and may be present as primary biological concentrations either with tissues in living condition and/or through sorption and formation of organometallic compounds. 相似文献