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1.
独居石微粒微区成分分布的研究 总被引：8，自引：0，他引：8
采用电子探针(EPMA)分析研究了花岗岩、伟晶岩 和热液交 代等三种不同成因的独居石微粒微区成分分布的特征。分析数据表明,花岗岩和花岗伟晶岩 成因的独居石微粒中La和Ce的含量低, 而Sm、Gd、Y、Th的含量明显较高。热液交代成因的 独居石微粒中,La、Ce的含量高,而Gd、Th、Y的含量明显较低。根据微区剖面(0.18mm)元 素分布曲线,指出了La、Ce、Nd、P、Th、Si、Ca和U等元素表现出8～10个微环带成分不均匀分布的特点,并认为成矿溶液的地质环境、温压和微量元素含量变化是不均匀分布的主要 原因。 相似文献
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在野外地质调查的基础上,结合室内显微镜观察及电子探针分析测试,对新疆拜城波孜果尔碱性岩中的副矿物的矿物学特征和化学成分进行了研究.发现这些副矿物常以共生组合的形式产在碱性岩中,主要分布在石英二长闪长岩和石英二长岩中.烧绿石中U、Th和REE替代Ca、Na.独居石富含LREE,Th和LREE相互替代;根据独居石中w(La+ Ce) ＞40％和La/Nd比值在1.6～4.5,推断独居石为热液成因.磷钇矿中富含REE,且以HREE为主;w(Th)＞w(U).锆石中Zr/Hf比值在60％以上,符合碱性岩特征;其Th/U比值为0.6,属于岩浆锆石.星叶石中w(Rb2O)、w(Cs2O)较高.萤石中Y、Ce替代Ca.锆石中的钍石w(U)明显高于磁铁矿中钍石w(U).在石英二长岩中,烧绿石的w(CaO)、w(TiO2)、w(ZrO2)、w(U3O8),磷钇矿的w(Y2O3),星叶石的w(TiO2),萤石的w(Ca),氟碳铈镧矿的w(CaO)较丰富;而在石英二长闪长岩中,烧绿石的w(Ce2O3),磷钇矿的REE含量,星叶石的w(Nb2O5)、w(Rb2O),萤石w(Ce)、w(Y)和氟碳铈镧矿的w(La2O3)较高. 相似文献
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西秦岭温泉钼矿床矿石矿物特征及钼的赋存状态 总被引：2，自引：1，他引：1
通过显微镜鉴定、电子探针（EPMA）及X射线粉晶衍射法等方法,首次对温泉钼矿的矿物组合、矿石类型、矿石结构构造和钼的赋存状态进行了研究。结果表明,矿石矿物为中温热液成因,并受温泉斑岩体的控制;钼矿物主要为辉钼矿。辉钼矿的多型为2H型（六方晶系）,为自形—半自形,呈细小鳞片状、片状、板条状分布于岩石中;辉钼矿的粒度主要集中在0.08-0.16 mm粒级范围,占总量的51.65%;黄铁矿中钼含量较高,且形成越早钼含量越高。 相似文献
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华南扬子地块是我国古热水沉积成矿作用最为发育的地区之一,其热水沉积特性最早引起我国学者的关注。华南下寒武统黑色岩系中赋存多个与热水沉积成矿作用相关的大型、超大型重晶石矿床与N i-Mo-U-V多金属富集层。进一步研究分布在华南扬子地块黑色岩系中的金属、非金属矿床成因及其地球化学特征,对认识华南乃至全球晚震旦—早寒武世生物与环境演化有着十分重要的意义。本文对华南下寒武统镍-钼富集层矿石进行电子探针研究,识别出黄铜矿、黝铜矿等铜的独立矿物;闪锌矿等锌的独立矿物;方铅矿、白铅矿等铅的独立矿物。研究表明,在镍-钼矿石中这些矿物的发现为镍-钼矿层是热水沉积作用产物提供了直接的矿物学证据。 相似文献
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独居石成因特征与U-Th-Pb定年及三江特提斯构造演化研究例析 总被引：8，自引：7，他引：1
独居石U-Th-Pb定年在地质年代学研究中占有重要地位,但其成因类型的识别和年龄值的合理地质解释始终是研究的难点。论文通过对比分析岩浆、热液和沉积成因独居石的内部结构、矿物组合以及稀土和微量元素地球化学特征,厘定了不同成因类型独居石的鉴别标志;并以三江特提斯构造演化研究为例,探讨了独居石的U-Th-Pb定年及其合理地质应用。不同地质环境中形成的独居石具有不同的内部结构和矿物组合及元素组成:岩浆独居石可能存在较宽且平直的岩浆环带,常与磷钙钍石共生;相对富集重稀土,具有较高的Y、Sc、Th、U、Sm、Gd等含量和Th/U比值,较低的La、Ce含量和稀土总量,显示为Eu强烈亏损的右倾斜分布模式。而热液独居石可能存在与流体作用有关的扇形环带,常与斜钍石共生;沉积独居石形态多不规则,与自生矿物相伴生。它们具有典型的四分组稀土分布模式,稀土总量较高,相对富集轻稀土(如La、Ce),贫Y、Sc、Th、U、Sm、Gd等,Th/U比值较低。独居石U-Th-Pb定年限定了松潘-甘孜造山带204~190Ma的早期变质作用和168~158Ma的局部热干扰,约140~130Ma冈底斯浅色花岗岩的形成与地壳的缩短加厚及快速隆升作用,约33~22Ma 红河断裂带与伸展作用有关的岩体侵位和左行走滑运动年代(且北部的去顶剥蚀作用要比中部早9Ma),约8~11Myr的东喜马拉雅构造结"挤出"构造变形时限。 相似文献
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近年来,在秦岭造山带宁陕伟晶岩区发现了数条Be-Nb稀有金属伟晶岩矿脉。本文通过扫描电镜和电子探针分析了Be-Nb伟晶岩中独居石的矿物学特征和矿物成分。研究结果表明,伟晶岩脉中的独居石可分为两类:Ⅰ类独居石主要分布在石英、长石等造岩矿物内部,在背散射图像中多数Ⅰ类独居石内部均匀,部分可见振荡环带,具有较高的Th O2含量(7.0%～13.9%,平均10.5%);Ⅱ类独居石单矿物在背散射图像下同样显示内部均匀,但亮度明显低于Ⅰ类独居石,且Th O2含量较低(0.9%～4.4%,平均2.2%)。这指示了Ⅰ类独居石的岩浆成因和Ⅱ类独居石的热液成因。岩浆成因独居石具有较高的Th O2含量与独居石中磷钙钍石的类质同象替代密切相关。岩浆成因独居石的U-Pb测年结果为200.8±2.1 Ma,代表伟晶岩的成岩年龄,该年龄结果接近宁陕岩基中的二长花岗岩。岩浆和热液成因独居石的εNd值的范围为4.6～3.0,这与二长花岗岩的εNd值范围基本一致,说明区内Be-Nb伟晶岩与上述二长花岗岩的同源性。综上所述,本研究认为宁陕地区Be-Nb伟晶岩... 相似文献
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喷流沉积型矿床是矿床地质学研究的前沿课题,查明矿石中重要组分(镍和钼)的赋存状态是该类矿床地质学研究的重要内容。湘黔地区天鹅山-黄家湾、大坪-大浒镍钼矿带是典型的海底喷流沉积矿床,本文采集该矿区的样品,应用化学和光谱定量分析、偏光显微镜和X射线衍射、扫描电镜、电子探针等大型现代仪器相结合的分析手段,研究了矿石中镍和钼的赋存状态。化学和光谱分析确定矿石中镍含量为3.76％,钼含量为4.99％;偏光显微镜下观察发现金属矿物零星分布,颗粒细小,结晶程度差,光学特征极不明显,晶体形貌特征难以观察,初步推断矿石矿物以胶状形式存在,但在光学显微镜下很难为这些矿物定名和描述;X射线衍射分析验证了偏光显微镜鉴定结果,印证了样品中存在很多非晶质矿物,仅有钨钼钙矿和镍黄铁矿两种矿物含有镍钼,且矿物含量很低(分别为0.4%和0.8%),对比化学分析结果,可推断样品还存在其他富含镍钼元素的矿物。进一步对富集镍钼元素的区域进行电子探针分析,最终确定了镍除了赋存于辉砷镍矿、方硫镍矿中,在胶状黄铁矿和磁黄铁矿边缘呈蠕虫状花边的镍黄铁矿中也有富集;钼主要赋存于碳硫钼矿中。矿石中的镍钼主要赋存于由胶态向结晶态过渡的金属矿物中,研究成果为该类矿床的矿石矿物学研究、选矿、冶炼及矿石综合利用提供重要的信息和依据。 相似文献
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河南舞阳铁山庙式BIF铁矿的矿物学与地球化学特征及对矿床成因的指示 总被引：4，自引：2，他引：2
河南舞阳铁矿位于华北克拉通南缘.铁山庙式铁矿是舞阳铁矿的一部分,赋存于新太古界太华杂岩铁山庙组表壳岩中.本文根据铁山庙式铁矿中三种不同类型矿石(条带状石英-辉石-磁铁矿、块状辉石-磁铁矿、块状石英-磁铁矿)中磁铁矿的矿物成分、全岩/矿的主量元素及微量元素特征,探讨铁山庙式铁矿床的成因.磁铁矿单矿物成分分析表明,条带状石英-辉石-磁铁矿矿石中磁铁矿的FeOT含量90.6％ ～93.1％,平均91.8％;块状辉石-磁铁矿矿石中磁铁矿的FeOT含量90.7％～91.2％,平均91.0％;块状石英-磁铁矿矿石中磁铁矿的FeOT含量92.0％～93.0％,平均92.4％.上述平均值均与磁铁矿FeOT的理论值(93.1％)接近.三种类型矿石的其它元素如TiO2、MgO、MnO、CaO、Al2O3 Cr2O3 NiO等含量均＜0.1％,无明显区别,表明该区磁铁矿为含杂质极少的纯磁铁矿,表现出沉积变质成因磁铁矿的特征.矿石中斜方辉石-单斜辉石及近矿围岩紫苏辉石-长石-石英矿物组合,表明铁山庙式矿床经受了高级变质作用,石英、磁铁矿等矿物普遍发生变质重结晶,颗粒粗大,但仍保存原有的地球化学组成.元素地球化学分析显示,三种类型矿石中SiO2 、TiO2 Al2O3、P2O5的含量相近;块状辉石-磁铁矿较其它二者相对贫铁、富钙、镁,这是由于块状辉石-磁铁矿石中富含铁普通辉石和铁次透辉石所致;矿石中TiO2、Al2O3含量都极低,说明该区成岩成矿过程中未受到碎屑物质的混染.三种不同类型矿石的主量元素含量总体上都与世界典型BIF的相近.对于稀土元素,三种类型矿石均具有轻稀土亏损、重稀土富集((La/Yb)PAAS=0.29～0.995＜1),La、Eu、Y的正异常(La/La*=1.10～1.89;Eu/Eu* =1.30～2.23;Y/Y* =1.47～1.84),较高的Y/Ho比值(39.7 ～51.3),具有现代海水及高温热液混合特征.因此,我们认为铁山庙式铁矿三种不同类型的矿石是极少受到陆源碎屑混染的化学沉积成因,虽遭受后期变质作用,但仍属BIF型铁矿. 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
16.
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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The Samchampi-Samteran alkaline igneous complex (SAC) is a near circular, plug-like body approximately 12 km2 area and is emplaced into the Precambrian gneissic terrain of the Karbi Anglong district of Assam. The host rocks, which
are exposed in immediate vicinity of the intrusion, comprise granite gneiss, migmatite, granodiorite, amphibolite, pegmatite
and quartz veins.
The SAC is composed of a wide variety of lithologies identified as syenitic fenite, magnetite ± perovskite ± apatite rock,
alkali pyroxenite, ijolite-melteigite, carbonatite, nepheline syenite with leucocratic and mesocratic variants, phonolite,
volcanic tuff, phosphatic rock and chert breccia.
The magnetite ± perovskite ± apatite rock was generated as a cumulus phase owing to the partitioning of Ti, Fe at a shallow
level magma chamber (not evolved DI = O1). The highly alkaline hydrous fluid activity indicated by the presence of strongly
alkalic minerals in carbonatites and associated alkaline rocks suggests that the composition of original melt was more alkalic
than those now found and represent a silica undersaturated ultramafic rock of carbonated olivine-poor nephelinite which splits
with falling temperature into two immiscible fractions—one ultimately crystallises as alkali pyroxenite/ijolite and the other
as carbonatite. The spatial distribution of varied lithotypes of SAC and their genetic relationships suggests that the silicate
and carbonate melts, produced through liquid immiscibility, during ascent generated into an array of lithotypes and also reaction
with the country rocks by alkali emanations produced fenitic aureoles (nephelinisation process). Isotopic studies (δ18O and δ13C) on carbonatites of Samchampi have indicated that the δ13C of the source magma is related to contamination from recycled carbon. 相似文献