共查询到20条相似文献，搜索用时 125 毫秒
1.
康家湾铅锌矿床位于湖南省水口山矿田,矿体主要产于二叠系当冲组下段泥灰岩、硅质岩与栖霞组灰岩的层间硅化破碎带中。根据矿物组合和穿插关系,可将该矿床的成矿作用过程划分为3个阶段:黄铁矿-石英阶段、闪锌矿-方铅矿(黄铁矿)-石英阶段和方解石-闪锌矿-方铅矿阶段。流体包裹体研究表明,康家湾铅锌矿床黄铁矿-石英阶段的流体主要为中-高温(243～343℃)、中-高盐度(18.4%～33.8% NaCleqv)的流体;闪锌矿-方铅矿(黄铁矿)-石英阶段的流体为中-高温(278～352℃)、中-低盐度(1.1%～20.7% NaCleqv)流体;晚期方解石-闪锌矿-方铅矿阶段的流体为低温(125～191℃)、低盐度(0.2%～6.7%NaCleqv)的流体。其中,闪锌矿-方铅矿(黄铁矿)-石英阶段的流体发生了沸腾作用。激光拉曼分析结果显示,该矿床成矿期的石英和闪锌矿中的液体包裹体气相成分主要为H_2O。H-O、S同位素研究显示,康家湾铅锌矿床的成矿流体可能主要来源于岩浆水,并在运移过程中混合了大气水。结合矿床地质、流体包裹体和氢氧、硫同位素特征,流体混合导致温度、盐度降低和沸腾作用可能是导致康家湾铅锌矿床成矿物质发生大规模沉淀的重要因素。 相似文献
2.
新华龙钼矿床位于中国东北地区吉林省东部,是一个新发现的斑岩型钼矿床。矿床产于花岗闪长斑岩中。矿床成矿阶段包括石英-浸染状辉钼矿、石英-网脉状辉钼矿、石英-黄铁矿-黄铜矿、石英-多金属硫化物和石英-碳酸盐化5个阶段。流体包裹体实验结果表明：流体包裹体的类型主要为气液两相包裹体,其次为纯气相和纯液相包裹体,还有少量含子矿物的多相包裹体。流体包裹体的均一温度为172～385 ℃,盐度(w(NaCl))为8.51%～45.44%。从早阶段到晚阶段成矿流体温度具有规律的演化,均一温度分别为360～390 ℃、270～350 ℃、250～260 ℃、220～230 ℃、170～190 ℃。其中:含子矿物多相包裹体均一温度为272～385 ℃,盐度为35.79％～45.44％,密度为1.07～1.08 g/cm3;气液两相包裹体均一温度为172～381 ℃,盐度为8.51％～23.36％,密度为0.70～0.99 g/cm3。激光拉曼光谱分析表明,包裹体的气体成分主要为CO2、H2O、N2和CH4。包裹体岩相学及测温表明,流体由早期的高温、高盐度、含二氧化碳的含矿流体在主成矿阶段发生流体包裹体的沸腾、CO2逸出、温度降低等过程,导致大量金属硫化物沉淀。结合氢氧同位素特征,初步确定该矿床的成矿流体主要以岩浆水为主,后期有大气水的加入。流体沸腾是新华龙钼矿床成矿的重要机制。 相似文献
3.
黑龙江省三矿沟矽卡岩型铁铜矿床流体包裹体研究 总被引：11，自引：2，他引：9
对黑龙江省三矿沟矽卡岩型铁铜矿床内花岗闪长岩中石英斑晶、硫化物阶段及石英-碳酸盐阶段的石英、方解石中流体包裹体的岩相学、显微测温学和显微激光拉曼光谱分析等的研究结果表明,流体包裹体有富液相、富气相和含子矿物多相包裹体3种类型;花岗闪长岩石英斑晶中的含子矿物多相包裹体均一温度均值为4320C,盐度在30.92 wt%～63.91 wt%NaCl eqv.之间,平均为52.96 wt%NaCl eqv.,代表了高温、高盐度岩浆流体;硫化物阶段形成的黄铜矿磁铁矿矿石中流体温度主要介于323～424℃之间,盐度介于8.95 wt%～62.51 wt%NaCl eqv.之间;硫化物阶段形成的黄铜矿矿石中流体温度主要介于333～441℃之间,盐度介于8.28 wt%～65.32 wt%NaCl eqv.之间;石英-碳酸盐阶段流体温度主要介于124～140℃之间,盐度介于1.65 wt%～4.34 wt%NaCl eqv.之间.铁铜矿石均形成于高温、高盐度阶段,以岩浆热液为主,在成矿晚期,由于大气降水的混合,形成了少量低温、低盐度流体,成矿流体以富Na、K、Ca、Cl-和CO~2_3-的高盐度流体为特征,主体属于NaCl-H_2O-CO_2-H_2S-CH_4体系.成矿流体在300～400℃区间内发生了强烈的沸腾作用,导致大量金属硫化物和少量金属氧化物沉淀,沸腾作用对三矿沟铁铜矿床的形成起到至关重要的作用. 相似文献
4.
偃尾山铜银矿床是大兴安岭北段呼中-塔源成矿带内新发现的中小型矿床。矿床围岩蚀变呈面状分布,主要蚀变类型为硅化、碳酸盐化、黄铁矿化、伊利石化、高岭石化和绢云母化。热液成矿期可分为三个阶段:成矿早期石英-黄铁矿阶段(含少量黄铜矿)、主成矿期石英-斑铜矿-黄铜矿-辉铜矿(含铜硫化物)阶段和成矿晚期石英-碳酸盐-萤石阶段(含少量方铅矿和闪锌矿)。该矿床流体包裹体主要为富液相包裹体,也有少量纯气相包裹体,未见含子矿物包裹体。主成矿阶段流体包裹体均一温度为155℃~342℃,峰值集中在160℃~230℃,冰点温度在﹣3.3℃~﹣0.3℃,盐度为0.53%NaC_(leqv)~5.41%Na Cleqv;流体成分以K~+、Na~+、SO_4~(2-)为主,含少量Ca~(2+)和Cl~-,气相成分以H_2O为主,含少量的CO_2;流体δ~(18)O在-11.8‰~-13.72‰之间,δD变化范围在-105‰~-137‰之间。总体上,成矿流体为低温低盐度流体,流体来源主要是大气降水,成矿流体和矿床蚀变-矿化特征显示本矿床可能为高硫型浅成低温热液矿床。流体压力的突然降低可能是成矿物质沉淀的主要机制。偃尾山矿床可能代表了区域上同时代一种新的矿床类型,后续深入研究将有助于认识该区域成矿规律和找矿方向。 相似文献
5.
闹牛山浅成热液铜多金属矿床是大兴安岭中部浅成热液-斑岩铜多金属矿集区内重要的矿床之一,矿床产于早白垩统玛尼吐组陆相酸性火山岩中;矿体呈脉状、网脉状、角砾状产出,受断裂控制;金属硫化物主要为黄铜矿、黄铁矿、磁黄铁矿、毒砂等。热液成矿过程可划分为4个阶段:(Ⅰ)石英-黄铁矿-辉钼矿-毒砂阶段,(Ⅱ)石英-黄铁矿-磁黄铁矿-黄铜矿阶段,(Ⅲ)石英-闪锌矿-方铅矿-黄铜矿阶段和(Ⅳ)石英-碳酸盐阶段。实验数据表明:流体包裹体的类型可分为纯气相包裹体(V型)、纯液相包裹体(L型)、气液两相盐水溶液包裹体(W型)和含子矿物的三相包裹体(S型),其中以W型居多。从早到晚矿化阶段流体发生了一系列连续变化,均一温度分别为405℃~260℃,407℃~183℃,368℃~170℃和183℃~109℃,盐度w(NaCleq)依次为3.05%~43.83%,0.35%~46.56%,0.35%~8.67%和0.71%~3.69%。激光拉曼光谱分析表明成矿流体属于H_2O-NaClCO_2±CH_4±(Mg/Ca)CO_3体系。氢-氧同位素分析结果显示,大兴安岭中段浅成热液铜矿床的初始含矿流体为残余岩浆水,成矿过程中,大气降水逐渐混入,成矿晚期演化为大气降水。综合分析认为闹牛山浅成热液铜多金属矿床成矿的主要机制是流体沸腾和混合作用,流体混合作用在主成矿期及成矿中晚期发挥着更重要的作用。 相似文献
6.
河南洛宁沙沟Ag-Pb-Zn矿床银的赋存状态及成矿机理 总被引：4，自引：0，他引：4
位于河南洛宁境内的沙沟热液脉型Ag-Pb-Zn矿床是熊耳山地区近年来新发现的大型矿床.野外观察和矿相学研究表明成矿过程包含4个阶段, 分别为石英-菱铁矿阶段(Ⅰ)、石英-闪锌矿阶段(Ⅱ)、石英-银矿物-方铅矿阶段(Ⅲ)和石英-碳酸盐阶段(Ⅳ), 其中Ⅱ、Ⅲ阶段为主成矿阶段.扫描电子显微镜-能谱分析(SEM-EDS)和电子显微探针微区成分分析(EMP)结果显示, 沙沟矿床中的银以不可见银和可见银两种形式存在, 但以可见银为主.不可见银主要以次显微包体(< 1 μm)的形式被包裹在黄铜矿和闪锌矿等硫化物中, 而可见银通常以各种银的独立矿物形式交代方铅矿和黄铜矿等硫化物或充填在硫化物和石英的显微裂隙内.结合本文研究和前人对沙沟矿床流体包裹体的研究认为, 银和铅、锌等金属离子在成矿早期高温阶段以氯络合物的形式搬运, 随着成矿热液温度和氧逸度的降低以及pH值的升高, 氯络合物因稳定性降低而解体, 硫氢络合物成为银、铅、锌的主要迁移形式.随着成矿热液温度的继续降低, 铅、锌等金属硫氢络合物开始分解, 方铅矿、黄铜矿和闪锌矿等硫化物得以沉淀, 此时部分银以显微和次显微包体银的形式被包裹于这些硫化物中.铅锌硫化物的大量沉淀引起成矿热液组成和性质的显著变化, 最终导致银从硫氢络合物中彻底解体, 并与Cu+、Sb3+等离子结合形成大量独立银矿物(如含银黝铜矿、硫锑铜银矿和辉铜银矿等), 而溶液中过饱和的银则以自然银的形式沉淀. 相似文献
7.
吉林大黑山钼矿床位于兴蒙造山带东缘,为一典型的超大型斑岩型钼矿床,矿体主要产于花岗闪长斑岩岩体内。矿床的成矿阶段包括石英-黄铁矿、石英-磁黄铁矿-黄铁矿、石英-辉钼矿、石英-多金属硫化物和石英-碳酸盐化5个阶段。流体包裹体研究结果表明:流体包裹体的类型主要为气液两相包裹体,其次为纯气相和纯液相包裹体,还有少量含子矿物的三相包裹体。流体包裹体的均一温度为160℃~417.6℃,盐度为4.48%~41.05%。从早阶段到晚阶段成矿流体的温度具有规律的演化,均一温度分别为400℃~417.6℃,340℃~378℃,230℃~340℃,218℃,160℃~185℃。其中含子矿物三相包裹体均一温度为320℃~405℃,盐度为34.43%~41.05%,密度为0.94g/cm3~1.03g/cm3;气液两相包裹体均一温度为160℃~417.6℃,盐度为4.48%~13.55%,密度为0.62g/cm3~0.97g/cm3。激光拉曼光谱分析表明,气液两相包裹体成分主要为CO2。氢氧同位素研究结果显示,该矿床的成矿流体主要以岩浆水为主,后期有大气水的加入。流体沸腾是大黑山钼矿床成矿的重要机制。 相似文献
8.
卓玛矿床位于云南香格里拉格咱弧东北部,属斑岩-热液脉型铜多金属矿床。矿体主要赋存于矿区石英二长斑岩内及附近,严格受NW向断裂控制。卓玛矿床的形成经历了黄铁矿-石英(Ⅰ)、黄铁矿±黄铜矿--石英(Ⅱ)、黄铁矿±黄铜矿±方铅矿±闪锌矿-石英(Ⅲ)及贫硫化物-石英-碳酸盐(Ⅳ)四个成矿阶段。通过对各成矿阶段研究样品石英颗粒中的原生流体包裹体进行岩相学、显微测温学及激光拉曼光谱研究,探讨卓玛铜多金属矿床成矿流体特征,结果表明:Ⅰ阶段石英中主要发育富CO_2及气液两相型包裹体;Ⅱ阶段石英中主要发育碳质、富CO_2、含CO_2及气液两相4种类型包裹体;Ⅲ阶段石英中主要发育含CO_2及气液两相型包裹体;Ⅳ阶段石英中主要发育富CO_2、含CO_2及气液两相3种类型包裹体。激光拉曼光谱显示碳质包裹体主要成分为CO_2和CH_4,而CO_2包裹体中除CO_2和CH_4气相成分外,还有部分H_2O。因此,综合研究结果显示卓玛铜多金属矿床成矿流体为中温、低盐度的CO_2--CH_4-Na Cl--H_2O体系热液。成矿过程中,流体温度和盐度数值略有降低趋势,成矿流体的不混溶作用是导致成矿物质大量卸载的关键因素。 相似文献
9.
内蒙古克什克腾旗长岭子铅锌矿床是大兴安岭南段新发现的一个矿床,矿体赋存于下二叠统大石寨组海相火山岩建造中,矿体受夕卡岩控制。根据手标本中脉体穿插关系和岩石薄片中观察的矿物共生组合特征,文中将长岭子铅锌矿的成矿过程划分为4个阶段：干夕卡岩阶段、湿夕卡岩磁铁矿阶段、石英硫化物阶段和石英碳酸盐阶段,分别以石榴子石±透辉石±硅灰石、石英+绿帘石+电气石+磁铁矿、石英+黄铁矿±磁黄铁矿±黄铜矿±方铅矿±闪锌矿和石英±方解石的矿物组合为标志。长岭子矿床主要发育水溶液包裹体(W型)和含子矿物多相包裹体(S型),前者可进一步划分为富液相(WL型)和富气相(WV型)两个亚类。干夕卡岩阶段辉石中主要发育S型和WL型包裹体,湿夕卡岩磁铁矿阶段绿帘石和石英中主要发育WL型、WV型和S型包裹体,石英硫化物阶段石英中可见所有类型的包裹体,石英碳酸盐阶段的石英±方解石脉中仅见WL型包裹体。干夕卡岩阶段辉石中流体包裹体的均一温度和盐度分别为387~524 ℃和10.7%~52%(NaCleqv.);湿夕卡岩磁铁矿阶段包裹体均一温度为312~533 ℃,盐度为11.3%~60%(NaCleqv.);石英硫化物阶段包裹体均一温度介于182~329 ℃,盐度介于4.7%~38%(NaCleqv.);石英碳酸盐阶段包裹体均一温度为124~199 ℃,盐度介于3.1%~22.4%(NaCleqv.)。上述矿床地质和成矿流体特征表明长岭子铅锌矿为夕卡岩型矿床。成矿流体经历了自夕卡岩阶段高温、高盐度岩浆热液向石英碳酸盐阶段低温、低盐度大气降水热液的转变。石英硫化物阶段发育沸腾包裹体组合,表明成矿流体发生了沸腾作用,这可能是成矿物质沉淀的主要机制。 相似文献
10.
西藏班-怒带西段荣那铜（金）矿床流体包裹体特征及矿床成因 总被引：2，自引：0，他引：2
荣那铜(金)矿床是班公湖-怒江缝合带西段新发现的矿床,是多龙矿集区的重要组成矿床之一,已探明储量达大型规模,具有超大型矿床的成矿潜力。荣那铜(金)矿床矿石矿相学与岩相学研究显示其具有典型高硫化型浅成低温热液型矿床的矿物组合(明矾石、硫砷铜矿等)和矿化蚀变特征。通过资料收集与野外观察,本文将荣那铜(金)矿床的成矿过程划分为石英-黄铁矿阶段、石英-多金属硫化物阶段与碳酸盐阶段,其中石英-多金属硫化物阶段为主成矿阶段。为查明该矿床的成矿流体特征,进一步确定矿床成因类型,对取自深部矿石中的石英脉(均为主成矿阶段含黄铁矿、黄铜矿石英脉)开展了流体包裹体的岩相学观察、显微测温和激光拉曼光谱分析。结果表明,上述矿物中主要发育富液相、富气相和含子矿物三相包裹体;富液相包裹体的均一温度与盐度分别为:80~440℃和4.63%~11.95%NaCl eqv;富气相包裹体的均一温度和盐度分别为:320~440℃和5.55%~10.74%NaCl eqv;含子矿物三相包裹体的均一温度与盐度分别为200~400℃和29.4%~32.56%NaCl eqv;富液相与富气相包裹体的气体成分除少量N2外,气体成分均为H2O。综合分析认为,荣那矿床成矿流体发生了强烈的沸腾作用,流体沸腾作用是该矿床的重要成矿机制。可见,荣那矿床具有高硫型浅成低温热液矿床的矿物组合及蚀变特征,但主成矿阶段石英脉流体包裹体特征与典型斑岩型铜(金)矿床的流体包裹体特征相似。因此,推测荣那高硫型浅成低温热液铜金矿的深部存在斑岩型铜金矿化,该矿床应属浅成低温热液型-斑岩型铜金矿床。 相似文献
11.
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
12.
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
13.
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
14.
《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
15.
16.
17.
《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
18.
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
19.
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
20.
Sulfide minerals in the Boulder batholith occur 1. as disseminated grains, visible in hand specimens; 2. in aplitic-pegmatitic pods and masses; 3. along joint and shear surfaces; 4. in hydrothermal veins; and 5. as minute masses within pyrite and silicate minerals and along intergranular sites. Hydrothermally altered rocks have an average sulfide content of 0.8 weight per cent, compared to an average of 0.01 per cent for unaltered rocks. Unaltered rock of the batholith may contain as much as 0.7 weight per cent sulfide. Sulfide inclusions in pyrite, the most abundant sulfide of the batholith, are common and represent a captured iss-phase which later changed to chalcopyrite plus pyrrhotite or mackinawite. Inclusions are most abundant, and more complex, in pyrites of hydrothermally altered and ore rocks. Electron-probe analyses show that pyrites of the Boulder batholith have very similar compositions to those found for pyrites from other ore deposits around the world. 相似文献