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1.
《矿物岩石》2018,(4)
巧家茂租铅锌矿是滇东北赋存于上震旦统灯影组白云岩地层中的代表性铅锌矿床之一,通过对5件不同产状矿体中与成矿有关的热液成因碳酸盐矿物白云石和方解石样品的C-O同位素示踪分析,发现成矿流体中的碳主要有3种来源:(1)白云石的δ~(13)C_(V-PDB)值介于0.6‰～3.5‰,δ~(18)O_(V-SMOW)值介于17.9‰～18.5‰,具有明显的海相碳酸盐岩去碳酸盐化来源特征;(2)方解石的δ~(13)C_(V-PDB)值主要集中于-5.7‰～-1.95‰,δ~(18)O_(V-SMOW)值介于13.80‰～17.5‰,来自碳酸盐岩的溶解作用;(3)下层矿的方解石δ~(13)C_(V-PDB)值出现了较大负值(δ~(13)C_(V-PDB)=-28.9‰),同时较高的氧同位素值(δ~(18)O_(V-SMOW)=17.6‰)显示有机物氧化来源的有机碳同位素组成特征。综合前人的研究成果,认为茂租铅锌矿的形成与二叠纪峨眉山玄武岩浆热液无关,成矿物质除了前人认为的来源于基底地层和赋矿地层,区域上泥盆系碳酸盐岩也是重要的铅锌源。 相似文献
2.
易门铜厂矿床是滇中易门铜矿带中的Cu品位较低的大型矿床,是矿带中的一种代表性矿床。矿区发育沉积-成岩型铜矿(铜厂式)和热液脉状铜矿(大尖山式)两种矿(化)体,成矿地质作用较特殊。本文系统分析两类矿体和赋矿碳酸盐地层的C、O同位素组成。结果表明,铜厂式矿石中白云石的δ~(13)C_(PDB)=-3.7‰~1.4‰,平均值-0.1‰,δ~(18)O_(SMOW)=19.7‰~21.7‰,平均值20.8‰,与赋矿碳酸盐地层(落雪组)中的白云石C、O同位素组成一致,均在正常海相沉积碳酸盐岩的范围,且受成岩期后作用的影响小,具有典型的沉积-成岩成因标志。尖山式矿体的脉石矿物方解石的δ~(13)C_(PDB)=-3.7‰~0.1‰(均值为-1.5‰),δ~(18)O_(SMOW)=11.9‰~17.0‰(均值为14.1‰),与沉积-成岩型矿体和赋矿碳酸盐地层的C、O同位素组成明显不同,在δ~(13)C_(PDB)-δ~(18)O_(SMOW)图上集中于岩浆碳酸岩与海相碳酸盐岩之间的狭小范围内,指示其成矿流体与幔源或深部岩浆活动有关,为壳-幔混合流体。其中壳源组分可能主要由矿区碳酸盐地层提供,而幔源组分则可能与晋宁-澄江期基性岩浆活动过程中的去气作用有关。C、O同位素组成证据说明,铜厂矿区层状铜矿和脉状铜矿的成矿作用类型不同,成矿流体也不具同源性,是典型的沉积-成岩型+热液叠加型矿床。 相似文献
3.
塔深1井寒武系白云岩储层同位素流体地球化学示踪 总被引：3，自引：0，他引：3
通过对塔里木盆地沙雅隆起阿克库勒凸起东部塔深1井寒武系白云岩岩石学特征及成岩成因分析,影响塔深1井寒武系地层流体改变主要成岩有准同生期、埋藏期和后期热液改造期等.塔深1井寒武系白云岩及充填孔、洞、缝内方解石的氧、碳、锶同位素地球化学特征表明:准生期白云岩δ~(13)C_(PDB)值(0.9‰～1.8‰)偏正、δ~(18)C_(PDB)值(-10.1‰～-4.2‰)偏负反映准同生期泥微晶白云石成因属于高盐度的海水使得碳酸盐泥发生白云石化;埋藏期白云岩碳、氧随重结晶作用加强,白云岩晶粒由细向粗变化值随埋深增加,由于同位素分馏作用而偏负,δ~(18)C_(PDB)值(-10.02‰～-5.7‰)呈明显的下降,但δ~(13)C_(PDB)值(-1.4‰～0‰)组成变化不大;后期热液白云岩在热液作用下δ~(18)C_(PDB)值普遍低于-10‰(δ~(18)C_(PDB)/‰-13.1～-9.4,δ~(13)C_(PDB)/‰-2～-0.647);基质方解石δ~(18)C_(PDB)值为-10.1‰～-10.13‰,δ~(13)C_(PDB)值为-1.48‰～-1.62‰;充填孔洞缝粗-巨晶方解石δ~(18)C_(PDB)值为-10.89‰～-14.28‰,δ~(13)C_(PDB)值为-2‰～-3.09‰,反映准同生期→埋藏期→后期热液晶粒大小由泥微晶→细晶→中晶→粗晶氧碳同位素值逐渐变小偏负,据~(87)Sr/~(86)Sr(0.707 284～0.746 888)值均远高于现今海洋中海水的锶同位素组成(0.708)及围岩的锶同位素(0.707 284),说明鞍形白云石以及方解石结晶时的孔隙流体不是残余在岩石孔隙中的同生期海水,而是外来的富含锶的流体,也就是深部热液流体.渗透回流白云石化、埋藏白云石化和高温热液白云石化等特征表明白云岩形成于超盐度、埋藏和高温热液等3种不同的环境,因此影响储层形成与分布,从而影响对白云岩的勘探. 相似文献
4.
藏北商旭造山型金矿床成矿物质来源探讨：C、S、Pb同位素证据 总被引：1，自引：0，他引：1
西藏双湖县商旭金矿床位于班公湖—怒江缝合带中段。矿床受近东西向断裂控制,赋存于中—下侏罗统木嘎岗日群浅变质增生混杂岩中。本文研究主成矿阶段石英流体包裹体中CO_2的C同位素及共生硫化物的S—Pb同位素组成特征,并与木嘎岗日群、虾别错—木嘎岗日山花岗岩等主要地质体对比。含金石英脉流体包裹体中CO_2的δ~(13)C_(V-PDB)值范围为-17.8‰～-23.1‰,均值为-21.3%,接近沉积岩或者变质岩源有机碳,表明商旭金矿床的成矿流体可能来自于木嘎岗日群的变质流体,而含金石英脉中发育着与虾别错—木嘎岗日山花岗岩同时代的少量岩浆锆石,暗示成矿流体还有岩浆热液的加入。共生硫化物δ~(34)S_(V-CDT)值变化于-4.5‰～4.6‰,均值为-1.6‰,具有深源硫(地幔或下地壳,δ~(34)S_(V-CDT)=-3‰～+3‰)的特征;共生硫化物Pb同位素位素[n(~(206)Pb)/n(~(204)Pb)=18.350～18.690、n(~(207)Pb)/n(~(204)Pb)=15.632～15.700、n(~(208)Pb)/n(~(204)Pb)=38.570～38.980]与早白垩世虾别错—木嘎岗日山花岗岩[n(~(206)Pb)/n(~(204)Pb)=18.558～19.169、n(~(207)Pb)/n(~(204)Pb)=15.616～15.651、n(~(208)Pb)/n(~(204)Pb)=38.838～39.154]基本一致,同时向侏罗统木嘎岗日群[n(~(206)Pb)/n(~(204)Pb)=18.630～18.970、n(~(207)Pb)/n(~(204)Pb)=15.619～15.673、n(~(208)Pb)/n(~(204)Pb)=38.887～39.260]略有漂移,暗示商旭金矿床的Pb可能来源于早白垩世岩浆活动,同时还有部分来自木嘎岗日群中铅的加入。本次研究认为,商旭金矿的成矿物质部分来自深部壳幔岩浆作用,并被成矿热液携带至浅部。木嘎岗日群围岩也贡献了部分成矿物质,被地层中的变质热液携带到成矿流体中。 相似文献
5.
滇西维西县铜厂箐铜矿床赋存于中侏罗统花开佐组二段粉砂质泥岩、粉砂岩夹泥灰岩中,受断裂构造控制呈脉状产出。本次通过研究与该矿床铜矿化关系密切的石英及方解石C-H-O同位素组成特征,揭示其成矿流体来源,进而探讨该矿床成因。研究发现,该矿床中主成矿阶段与铜矿共生的方解石样品的δ~(13)C_(V-PDB)值变化于-6.93‰～-6.16‰,均值为-6.69‰,δ~(18)O_(V-SMOW)值变化于10.88‰～13.07‰,均值为11.98‰;与铜矿共生的石英样品的δ~(18)O_(V-SMOW)值变化于14.22‰～16.88‰,均值为15.93‰,δD_(V-SMOW)值介于-87.0‰～-61.7‰,均值为-75.99‰,表明成矿流体主要源自岩浆水。结合区域地质背景,认为在喜马拉雅期印度-欧亚大陆碰撞背景下,由于澜沧江深大断裂和雪龙山断裂长期活动,伴有深部岩浆含矿热液沿构造裂隙充填,形成铜厂箐脉状铜矿床。 相似文献
6.
湘西花垣地区铅锌矿床是铅锌矿资源储量超过千万吨的世界级超大型矿床之一。对该矿床主矿化期的方解石和闪锌矿进行了系统的C、H、O同位素研究。分析结果显示,花垣地区铅锌矿床主成矿期方解石样品的δ~(13)C_(PDB)值范围为-2.71‰~1.21‰,δ~(18)OSMOW值范围为16.09‰~22.48‰,团结、李梅、土地坪、蜂塘和大石沟各铅锌矿床中主成矿期方解石的13C、18O同位素依次表现出逐渐降低的特征,在δ~(18)O_(SMOW)-δ~(13)C_(PDB)图上主要介于原生碳酸盐岩与海相碳酸盐岩之间,该地区铅锌矿床成矿流体中的碳主要来源于海相碳酸盐岩的溶解作用。花垣矿区围岩的δ~(13)C_(PDB)值范围为0.15‰~1.17‰,δ~(18)O_(SMOW)值范围为19.79‰~23.89‰,指示沉积成因海相碳酸盐岩的特征。方解石和闪锌矿样品中流体的δD_(SMOW)变化于-91.1‰~-15‰之间,δ18Ofluid变化范围为-4.1‰~9.25‰,在矿区范围内流体的迁移方向是由北向南,δ~(18)O_(fluid)-δD_(SMOW)图显示,矿床成矿流体的主要来源是建造水和大气降水。成矿流体与围岩间的水-岩反应是导致湘西花垣地区铅锌矿床中方解石和闪锌矿矿物发生沉淀的主要机制。 相似文献
7.
通过各类薄片显微镜下鉴定与定量统计,阴极发光、扫描电镜、电子探针、碳、氧及锶同位素、流体包裹体均一温度测试等分析,开展了白云凹陷深水区珠江组和珠海组砂岩储层中碳酸盐胶结物的类型与期次、地球化学特征、成因机制研究。结果显示,存在三期碳酸盐胶结作用,早期主要为方解石,以高Ca、低Fe、低Mg为特征。但珠江组早期碳酸盐胶结物的同位素组成(δ~(13)C_(PDB):-2.43‰~0.29‰,δ~(18)OPDB:-9.79‰~-3.08‰,87 Sr/86Sr:0.7084~0.7109)与珠海组(δ~(13)C_(PDB):-9.37‰~-8.13‰,δ~(18)OPDB:-7.11‰~-7.09‰,87Sr/86Sr:0.7138~0.7142)有一定差异,前者是在浅埋藏阶段从碳酸盐过饱和碱性海水介质中沉淀出的产物;后者与碳酸盐过饱和的碱性淡水有关。中期主要为铁方解石,以高Ca、较高Fe、低Mg、碳和锶同位素组成变化范围较大(δ~(13)C_(PDB):-20.88‰~-5.29‰,δ~(18)OPDB:-11.1‰~-8.99‰,87Sr/86Sr:0.7093~0.7151)为特征,其部分碳源与有机酸脱羧作用产生的CO_2有关,另一部分碳源(δ~(13)C_(PDB):-5.38‰~-5.29‰)可能与深部物质有关。形成碳酸盐胶结物所需的Ca2+、Mg2+、Fe2+等离子来源于砂岩中长石等碎屑的溶蚀、黏土矿物的转化以及深部热液流体。晚期主要为铁白云石(δ~(13)C_(PDB):-2.83‰~-1.83‰,δ~(18)OPDB:-9.45‰~-5.77‰,87Sr/86Sr:0.7101~0.7162),以高Fe、高Mg、较低Ca、碳同位素组成与同期海水基本一致为特征,87Sr/86Sr值低于正常成岩演化形成的碳酸盐,该期碳酸盐胶结物的形成与砂岩中生物碎屑以及先期碳酸盐胶结物的溶蚀再沉淀有关,部分可能受到深部热液流体的影响。 相似文献
8.
千家坪钒矿床产于南秦岭下寒武统水沟口组(缀1sh)黑色岩系中,该黑色岩系由黑色含炭硅质岩、含炭硅质岩夹泥岩和泥岩等组成。钒矿体呈层状产出,矿石以黑色硅质岩夹泥岩型为主,含钒矿物主要为钒云母。黑色岩系岩石主要成分为SiO2、Al2O3、K2O等,富集TFe、Ba、Zn、P、Cu、Ni、Cr、Sr、Zr、Ag、Ti、Mn、V等多种元素。黑色岩系n(V)/n(Cr)=5.92～30.64、n(V)/n(V+Ni)=0.88～0.99、δU1,判断其为缺氧沉积环境。黑色硅质岩n(SiO2)/n(Al2O3)=238.81,U/Th1以及δ30Si=-0.1‰～0.5‰、δ18O=20.2‰～25.8‰,判断其为半深海滞留沉积盆地热水沉积成因。泥岩n(SiO2)/n(Al2O3)=5.69,n(Al)/n(Al+Fe+Mn)=0.63,n(Si)/n(Si+Al+Fe)=0.74～0.76判断其物源为陆源,但受到热水作用影响。钒矿化受下寒武世古隆起边缘断陷滞留盆地中形成的黑色岩系层位所控制。钒明显趋向在炭硅质岩所夹的泥岩或硅质岩附近的泥岩中富集,在炭硅质岩夹泥岩段向泥岩段过渡层位,常常含结核,钒元素含量达到峰值,其他Cu、Pb、Zn、As、W、Mo等元素富集规律与V元素基本一致。该矿床成矿物质主要来源于深部热水,泥岩的吸附作用对钒的富集具有重要作用。综合地质、地球化学特征,认为该矿床为热水喷流沉积成因。 相似文献
9.
湖北徐家山锑矿床方解石C、O、Sr同位素地球化学 总被引：4，自引：0，他引：4
湖北通山的徐家山锑矿床产在上震旦统陡山沱组和灯影组的海相碳酸盐岩中.对该矿床中成矿前和成矿期方解石进行了较系统的C、O、Sr同位素地球化学研究,结果表明,成矿前方解石具相对较高的δ13CPDB(-0.7‰～ 2.0‰)、δ18OSMOW( 18.6‰～ 19.6‰)和Sr含量(2645-8174 μg/g,平均5656μg/g),及较低的87Sr/86Sr比值(0.7096～0.7097);而成矿期方解石具相对较低的δ13CPDB(-3.9‰～-2.1‰)、δ18OSMOW( 11.5‰～ 15.3‰)、Sr含量(785～2563μg/g,平均1571μg/g),和较高的87Sr/86Sr比值(O.7109～0.7154,平均0.7141).分析认为,成矿前方解石的C、O和绝大部分Sr来源于赋矿围岩--震旦系海相碳酸盐岩;而成矿流体为富H2CO3的溶液,它来自或流经富放射成因87Sr的下伏基底碎屑岩--中元古界冷家溪群浅变质岩;该流体与围岩发生水.岩反应导致成矿期方解石和辉锑矿的沉淀. 相似文献
10.
《地质科技情报》2020,(3)
渝东石柱地区志留系龙马溪组页岩地层发育特殊的纤维状方解石脉体。为揭示其流体来源及形成机理,结合岩石学及地球化学特征等开展系统分析。研究表明,纤维状方解石脉(FCV)以顺层或近平行层面充填于黑色粉砂质页岩和泥质粉砂岩微裂缝中,脉体宽0.1～4.0 cm、横向延伸一般为0.5～8.0 m。纤维状方解石晶体以柱状、纤维状垂直裂缝壁生长为主,多与石英共生产出。晶体表面洁净,局部见方解石压力影、机械双晶及晶体间锯齿状晶界。阴极发光下纤维状方解石呈暗红色-橘红色;碳-氧同位素分析表明δ~(13)C_(PDB)略偏负、δ~(18)O_(PDB)负异常明显(δ~(13)C_(PDB)、δ~(18)O_(PDB)平均值分别为-1.549‰及-12.654‰),指示其形成过程中受温度升高影响明显;流体包裹体均一温度平均值为159.5℃。结合区域构造-热演化史分析,结果表明石柱地区龙马溪组FCV形成流体具造山带同构造期超高压有机流体性质特征,为中-晚三叠世印支期同构造作用驱动深部流体叠加生烃超高压释放导致水力压裂所致,裂缝的开启导致孔隙流体的过饱和及纤维状方解石的快速沉淀。 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.
《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
17.
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