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青海沱沱河地区多才玛铅锌矿床成因:原位S和Pb同位素证据 总被引：2，自引：2，他引：0
青海沱沱河地区多才玛铅锌矿床是西南三江特提斯北段新生代铅锌矿集区的典型矿床之一,本文首次应用飞秒激光剥蚀多接受器等离子体质谱法对多才玛铅锌矿床中金属硫化物的原位S和Pb同位素进行了测定。结果显示:黄铁矿、方铅矿和闪锌矿的原位S同位素的δ~(34)S_(V-CDT)值介于-26.34‰～4.24‰之间,均值-12.15‰(n=20),其中闪锌矿的δ~(34)S_(V-CDT)值介于-10.30‰～-3.52‰,均值-7.39‰(n=9);方铅矿的δ~(34)S_(V-CDT)值为-26.34‰～-11.74‰,均值-20.36‰(n=9);黄铁矿的δ~(34)S_(V-CDT)值分别为2.50‰,4.24‰。矿床δ~(34)S数据范围较宽,总体表现为富集负值硫的特征,说明有机质可能参与成矿。岩浆热液期发育的黄铁矿δ~(34)S值具有深源特征,沉积热液期发育的方铅矿和闪锌矿的δ~(34)S值表明成矿过程存在还原作用,指示盆地地层还原流体的混入,综上可认为多才玛铅锌矿床硫具有混合来源的特征。方铅矿原位Pb同位素结果为~(206)Pb/~(204)Pb=18.866～18.929,~(207)Pb/~(204)Pb=15.674～15.689,~(208)Pb/~(204)Pb=39.052～39.174。方铅矿与地层的Pb同位素组成一致,位于上地壳平均Pb演化线之上,具上地壳和地幔混合俯冲带铅的特征,表明其成矿物质的来源多样。结合矿床学、矿物学及同位素数据,本文认为多才玛铅锌矿床S元素主要来源于赋矿围岩,Pb金属元素主要来源于藏北钾质火山岩,侵入地层岩浆与盆地流体的混合是金属硫化物沉淀的重要机制。 相似文献
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《矿物岩石地球化学通报》2016,(6)
为探讨会泽铅锌矿田成矿流体总硫同位素组成、成矿温度、硫源及还原硫的形成机制,在分析前人的硫同位素数据基础上对麒麟厂矿床上部原生矿体硫化物(黄铁矿、闪锌矿和方铅矿)及麒麟厂和矿山厂矿床外围新发现的硫酸盐矿物(重晶石)进行了硫同位素研究。结果显示,原生矿体中的硫化物的δ34S变化为8.0‰~17.68‰,成矿流体中硫同位素已达分馏平衡;矿床外围的硫酸盐δ34S变化为17.95‰~24.30‰。利用共生矿物对Pinckney法,估算获得成矿流体的δ34SΣS为14.44‰,与海相硫酸盐的δ34S相近;通过同位素地质温度计,估算获得成矿温度为134~388℃;包裹体测温发现,重晶石为热液成因,暗示成矿流体中的硫可能来自矿区及矿区外围各个地层的海相硫酸盐或是矿区发现的热液重晶石。硫酸盐的还原机制应为热化学还原作用(TSR)。 相似文献
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滇西镇康水头山Pb-Zn矿床成矿流体及矿质来源探讨——H、O、S、Pb同位素地球化学证据 总被引：2，自引：1，他引：1
滇西镇康水头山Pb-Zn矿床是保山地块镇康Pb-Zn-Fe-Cu多金属矿集区内又一重要找矿成果。矿体呈似层状、透镜状产于上寒武统保山组大理岩化灰岩中,呈NEE向顺层产出,矿石矿物主要为闪锌矿和方铅矿,偶见黄铜矿和黄铁矿等;脉石矿物主要有白云石、绿泥石、方解石、石英和绢云母等。本文基于对矿床地质特征的详细研究,结合矿床H、O、S、Pb同位素组成,对其成矿流体和矿质来源进行了探讨,同时与毗邻的芦子园超大型Pb-Zn-Fe-Cu多金属矿床进行了对比。研究表明:该矿床石英的δD值介于-101.1‰~-93.3‰之间,均值为-96.85‰(n=4),δ~(18)O_(H_2O)值为3.37‰~3.77‰之间,均值为3.57‰(n=4),表明成矿流体早期以原生岩浆水为主,有大气降水的混入。矿床金属硫化物的δ~(34)S值均为正值,介于4.1‰~12.2‰,均值为8.23‰(n=10),与旁侧的芦子园矿床δ~(34)S值(8.9‰~12‰)较为接近。该矿床可划分出三个成矿阶段,阶段Ⅱ为以闪锌矿和方铅矿为主的主要成矿阶段(δ~(34)S主要集中在4.1‰~6.2‰之间),其δ~(34)S均值可近似代表成矿热液中的δ~(34)S∑S值,即δ~(34)S∑S≈δ~(34)S均值=6.56‰(n=7),闪锌矿和方铅矿δ~(34)S值有部分重叠,但总体上具有δ~(34)S闪锌矿δ~(34)S方铅矿以及不同颜色闪锌矿之间δ~(34)S深棕色闪锌矿δ~(34)S棕褐色闪锌矿δ~(34)S浅棕色闪锌矿的分布特征,暗示硫同位素在硫化物间的分馏达到平衡,表明S同位素组成较为稳定,显示水头山矿床具有深部壳源岩浆成因的特征。矿床金属硫化物的Pb同位素分析显示,Pb同位素组成非常集中(~(206)Pb/~(204)Pb=18.3408~18.4483,均值为18.3815,~(207)Pb/~(204)Pb=15.8337~15.9440,均值为15.8745,~(208)Pb/~(204)Pb=38.8224~39.4391,均值为38.9941,n=10),投点主要分布在上地壳演化线上方,表明其Pb主要来自于以岩浆作用为主的上地壳物质。本文认为矿区深部壳源岩浆热液是水头山矿床最重要的成矿流体与矿质来源,流体的混合作用是矿床金属元素沉淀和富集的重要机制,矿床具有低温、后生成矿特征,推测矿床的形成与燕山晚期的岩浆热液作用有关。 相似文献
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贵州普定纳雍枝铅锌矿矿床成因:S和原位Pb同位素证据 总被引：12，自引：5，他引：7
通过近五年(2011~2015)勘查实现找矿重大突破的贵州普定纳雍枝铅锌矿床,位于扬子陆块西南缘,五指山背斜南东翼北中部,是黔西北铅锌成矿区的重要组成部分。矿区内已发现20余个铅锌矿体,探获铅锌金属资源储量超135万吨,是川滇黔接壤铅锌矿集区贵州境内目前已发现和探明规模最大的铅锌矿床。主矿体多呈层状、似层状、透镜状和陡倾斜脉状产出,除了陡倾斜脉状矿体产于F7断层破碎带,其余(似)层状矿体均产于下寒武统清虚洞组和上震旦统灯影组白云岩中,与围岩产状一致,层控特征明显。其矿石类型主要有块状、角砾状、细脉状和浸染状等,矿石矿物以闪锌矿为主,其次为方铅矿和黄铁矿,脉石矿物以方解石、白云石为主,含少量石英,偶见重晶石。本次研究表明,该矿床硫化物δ~(34)S_(CDT)值介于15.94‰~25.49‰之间,均值为22.41‰(n=21),其中黄铁矿δ~(34)S_(CDT)值为22.06‰,闪锌矿δ~(34)S_(CDT)值为19.37‰~25.49‰,均值为23.17‰(n=17),方铅矿δ~(34)S_(CDT)值为15.94‰~19.70‰(n=3),均值为18.23‰。各类硫化物δ~(34)S值部分重叠,总体上不具有δ~(34)S黄铁矿δ~(34)S闪锌矿δ~(34)S方铅矿的特征,暗示硫同位素在硫化物矿物间的分馏未达到平衡。此外,矿石存有少量硫酸盐矿物(重晶石),暗示成矿流体的δ~(34)S3∑S值应高于硫化物的平均δ4S值(22.41‰),接近赋矿地层中海相硫酸盐岩的δ~(34)S值(22‰~28‰)。因此,成矿流体中的还原硫最可能为海相硫酸盐岩热化学还原的产物,来源于赋矿地层中的蒸发岩。应用飞秒激光剥蚀多接收器等离子体质谱法首次获得了纳雍枝铅锌矿中方铅矿原位Pb同位素数据,结果显示Pb同位素组成非常集中(~(206)Pb/204Pb=17.828~17.860,均值17.841,~(207)Pb/204Pb=15.648~15.666,均值15.659,~(208)Pb/204Pb=37.922~37.979,均值37.960,n=32),位于上地壳平均Pb演化曲线上,表明其成矿物质具壳源特征,可能来源于基底岩石。综合矿床地质、矿物学、S和原位Pb同位素数据,本文认为纳雍枝铅锌矿床S主要来源于其赋矿地层,Pb等金属元素主要来源于基底岩石,这两组流体的混合是导致其金属硫化物沉淀成矿的重要机制,成矿流体具后生、低温热液等特征,属于密西西比河谷型(MVT)矿床,很可能形成于燕山期,与右江盆地演化有关。 相似文献
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近年来，在相山铀矿田的西部牛头山地区深部发现了铅锌矿化体，其成因机制不明.为探讨牛头山铅锌矿化体物质来源，开展了硫化物原位硫同位素分析研究.根据硫化物矿物之间的充填和包裹关系判断，铅锌矿化体金属硫化物形成的先后顺序是:黄铁矿形成最早，方铅矿和闪锌矿次之，细脉状黄铜矿形成最晚.利用LA-MC-ICP-MS技术对矿化体中几种金属硫化物分别进行了系统的原位硫同位素分析.结果显示:黄铁矿、闪锌矿、方铅矿、细脉状黄铜矿的δ34S值介于-4.8‰~+5.4‰之间，各硫化物矿物之间硫同位素未达到完全平衡分馏，利用黄铁矿δ34S值得到的矿化流体δ34SΣS值（总硫同位素组成）近似为+3.7‰，与共生矿物对（闪锌矿-方铅矿）图解法得到的闪锌矿和方铅矿沉淀时矿化流体的δ34SΣS值（+3.2‰）相近，表明形成牛头山铅锌矿化体的矿化流体δ34SΣS值大约为+3.7‰，为岩浆硫.结合前人的岩浆岩年龄数据，我们判断该铅锌矿化体金属硫化物的硫可能主要来自次火山岩相花岗斑岩岩浆热液.同一薄片中闪锌矿δ34S值高于共生的方铅矿，表明两者硫同位素基本平衡，利用共生矿物对（闪锌矿-方铅矿）硫同位素温度计计算得出平衡温度为197~476℃，与前人通过脉石矿物流体包裹体得到的铅锌矿化流体温度基本一致.相山火山盆地与相邻的北武夷黄岗山、梨子坑等产铅锌矿的火山盆地具有相似的成矿条件及成矿物质来源，使相山火山盆地具有良好的铅锌多金属找矿前景. 相似文献
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湖南宝山Pb-Zn多金属矿床硫同位素地球化学特征及其地质意义 总被引：1，自引：0，他引：1
湖南宝山Cu-Mo-Pb-Zn-Ag多金属矿床规模大、矿种多、分带明显,是南岭有色金属成矿带的代表性矿床之一。本文对该矿床的硫同位素组成进行了较系统的研究,以探讨该矿床成矿物质的来源。研究表明,硫化物硫同位素组成具有δ34S黄铁矿δ34S闪锌矿δ34S方铅矿特征,说明成矿流体中硫已达到分馏平衡;矿床硫化物的硫同位素组成均为较低正值,变化范围很窄,δ34S值主要集中在1.50‰~4.50‰之间,峰值在3‰左右,明显低于研究区石炭系碳酸盐岩硫同位素δ34S值(17.8‰~22.6‰),具岩浆硫特征,暗示成矿流体中硫主要来源于燕山期花岗闪长斑岩有关的岩浆分异,地层硫贡献较少。此外,不同围岩的矿体,硫化物δ34S值基本相同,围绕花岗闪长斑岩体δ34S值没有分带现象,表明硫的来源具有一致性。因此,有理由认为,赋存于下石炭统梓门桥组白云岩、测水组砂页岩和石凳子组灰岩中的Pb-Zn多金属矿化具有相同成因联系,它们应为同一岩浆-热液系统演化的产物。 相似文献
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通过塔西南缘铅锌矿带金属硫化物(方铅矿、黄铁矿、黄铜矿、闪锌矿)的硫同位素测试研究,结果显示δ34S值范围在-38.3‰～24.0‰,具双峰式分布,推测两种或两种以上流体相混合是导致矿床硫同位素组成变化的主要原因,一类硫化物的δ34S值集中在-6‰～6‰,组成的矿石呈细粒、草莓状结构及浸染状构造;另一类硫化物的δ34S值集中在-32‰～-24‰,组成的矿石呈粗粒、脉状或角砾状构造。两种流体受构造应力和压实作用的影响,沿着断裂或岩石的裂隙运移并相混合,发生热化学硫酸盐还原反应,产生的HS-与Zn2+、Pb2+结合形成闪锌矿、方铅矿,在有利部位沉淀成矿。硫主要来源于海水硫酸盐。 相似文献
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胶西北新城金矿床硫同位素地球化学 总被引：8，自引：6，他引：2
新城金矿床是胶西北金矿集区中典型的破碎带蚀变岩型金矿床,其热液成矿作用可划分为四个阶段:黄铁矿-石英-绢云母阶段(I)、石英-黄铁矿阶段(II)、石英-多金属硫化物阶段(III)和石英-方解石阶段(IV),其中金主要赋存于II和III阶段的黄铁矿内。该矿床赋矿围岩为郭家岭岩体,岩性为石英二长岩和二长花岗岩,主要为胶东群变质基底经部分熔融形成。胶东群变粒岩硫同位素较为均一(δ34S值介于6.9‰~9.4‰,均值为8.0‰);郭家岭岩体的δ34S值介于6.0‰~16.0‰,均值为8.6‰,反映了其硫同位素组成总体上继承了变粒岩的硫同位素特征;长英质脉岩的δ34S值变化范围为0.8‰~8.5‰(均值为6.7‰),其中4件样品的δ34S值变化范围为7.4‰~8.5‰,反映了其硫主要源自于郭家岭岩体,变粒岩可能提供了部分硫源;而其中1件样品的δ34S值仅为0.8‰,符合岩浆硫来源特征,表明深部岩浆可能也提供了部分硫源。新城金矿床矿石中硫化物δ34S值变化范围较大(4.3‰~10.6‰,均值为8.3‰),表明矿石硫可能源于郭家岭岩体、变粒岩和长英质脉岩,最终主要来源于胶东群变质基底。I阶段黄铁矿颗粒较小(5~600μm),晶形主要为立方体,反映其处于温度较高(300~350℃)、成矿流体的过饱和度较低、低氧逸度和硫逸度、冷却快速、物质供应不足的成矿环境;黄铁矿δ34S值变化范围为8.4‰~10.6‰,均值为9.7‰,反映了矿石硫可能源自于δ34S值较高的郭家岭岩体和变粒岩。II和III阶段黄铁矿粒径变化较大(3μm~2.5mm),晶形主要为五角十二面体,反映其处于中-低温度(200~300℃)、成矿流体过饱和度高、高氧逸度和硫逸度、缓慢冷却同时物质供应充分的成矿环境。其中,II阶段黄铁矿δ34S值变化范围为7.7‰~9.7‰,均值为8.7‰,表明矿石硫源除郭家岭岩体和变粒岩外,δ34S值较低的长英质脉岩可能也提供了部分硫源。III阶段硫化物δ34S值变化范围较大(4.3‰~9.4‰,均值为7.1‰),闪锌矿-方铅矿硫同位素热力学平衡温度范围为180~282℃,氧逸度约为10-37.3~10-36.8,反映了矿石硫源自于郭家岭岩体、变粒岩和长英质脉岩,硫化物δ34S值变化范围较大可能是硫同位素分馏达到平衡的结果。IV阶段黄铁矿粒径最小(1~5μm),为晶形完好、表面光滑的立方体晶形,表明其处于较低温度(200℃),成矿流体的过饱和度较低、氧逸度和硫逸度较低、物质供应不足的成矿环境。 相似文献
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分析了四川冕宁大型稀土矿床硫同位素组成.结果显示成矿期脉石矿物重晶石与矿化期后硫化物(黄铁矿和方铅矿)的硫同位素组成明显不同,前者富集34S,其δ34S为 1.8‰～ 6.7‰,后者富集32S,其δ34S在-10.9‰～-2.1‰之间,表明本区成矿流体中的硫和矿化期后富含硫化物流体中的硫具有不同的来源.矿区各种类型矿石中的重晶石均普遍遭受过风化作用,且δ34S随风化作用的增强而增加,暗示物理分馏效应是本区重晶石硫同位素组成差异的主要原因,重晶石风化过程实际上是一个贫32S、富34S过程,未风化重晶石的δ34S与典型幔源硫的δ34S(0‰左右)相近,成矿流体中硫主要来源于地幔.矿石中重晶石风化作用过程中被淋滤的32S可能是矿化期后富含硫化物流体中的硫的重要来源,但有待深入研究. 相似文献
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Alexey Kamyshny Jr. Clemens G. Borkenstein Timothy G. Ferdelman 《Geostandards and Geoanalytical Research》2009,33(3):415-435
A HPLC-based protocol has been developed for the determination of zero-valent sulfur (ZVS) speciation, including solid, colloidal elemental sulfur and individual inorganic polysulfides in natural aquatic samples. The protocol includes four experimental procedures: (1) determination of polysulfide speciation by rapid single-phase derivatisation with methyl trifluoromethanesulfonate; (2) determination of the sum of polysulfide and colloidal sulfur by reaction with hydrogen cyanide (cyanolysis); (3) determination of total zero-valent sulfur by treatment with zinc chloride followed by extraction with chloroform; and (4) chromatographic determination of polythionates without sample pre-treatment. With proper sampling and preservation techniques in the field or on board ship, this combination of methods allowed the quantitative determination of: (a) individual polysulfide species; (b) dispersed colloidal sulfur; (c) dispersed solid elemental sulfur; and (d) tetra-, penta- and hexathionates. With minor modification, the method could be expanded to include other polythionates. Sixteen various wet chemical and liquid chromatographic methods were tested on nine synthetic reference samples (including solid elemental sulfur, colloidal elemental sulfur, inorganic polysulfides and polythionates) to establish the optimal protocol. The protocol was further evaluated by analysing the zero-valent sulfur content in microbially-produced sulfur and in sulfur from two natural samples of sulfide-rich seawater from tidal flats pools of the Wadden Sea (Germany). 相似文献
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Abstract. Isotope composition of whole rock sulfur has been measured on 14 schists, 10 gneisses, 7 gabbroids, 7 granitoids and 2 sedimentary rocks, with of 9 sulfide (pyrite) sulfurs in gabbros and granitoids, from the southwestern part of the Ryeongnam Massif, Korea. The δ34 S values of schists range from -4.6 to +6.1 % (average +0.9 %), those of gneisses from -4.0 to +0.8 % (-1.9%), those of gabbroids from -2.3 to +3.7 % (+1.0 %), and those of granitoids from -5.9 to +3.2 % (-1.9 %). The δ34 S values of pyrite separated from gabbros and granitoids show rather heavier values ranging from +3.1 to +9.4 % with an average of+5.8%.
Though the δ34 S values of whole rock sulfur give wide range of -5.9 to +6.1 %, the average of about -0.5 % is close to the mantle value. The granitoids sampled at the central parts of intrusive bodies or at the contacts with other plutonic rocks tend to show positive values, while those sampled near the boundary with basement rocks such as granitic gneiss and por-phyroblastic gneiss show negative values. Though the reason of this tendency is not clear at present, the δ34 S values of some granitoids in this area seem to represent possible influence by the assimilation of country rocks, particularly of gneisses.
Average isotopic compositions of ore sulfur from individual metal deposits in the studied area are summarized to have a range of+1.0 to +7.8 % with an average value of+3.2 %. The values are consistent with the previous finding that the ore sulfur isotopic values of the Ryeongnam Massif are the lowest among the four tectonic belts in Korea; Gyeonggi Massif, Ogcheon Belt, Ryeongnam Massif, and Gyeongsang Basin. This feature may reflect the isotopic compositions of plutonic rocks and basements in this area, which are characterized by relatively low values around zero permil. 相似文献
Though the δ
Average isotopic compositions of ore sulfur from individual metal deposits in the studied area are summarized to have a range of+1.0 to +7.8 % with an average value of+3.2 %. The values are consistent with the previous finding that the ore sulfur isotopic values of the Ryeongnam Massif are the lowest among the four tectonic belts in Korea; Gyeonggi Massif, Ogcheon Belt, Ryeongnam Massif, and Gyeongsang Basin. This feature may reflect the isotopic compositions of plutonic rocks and basements in this area, which are characterized by relatively low values around zero permil. 相似文献
14.
Jens Gröger Jennifer Franke Kay Hamer Horst D. Schulz 《Geostandards and Geoanalytical Research》2009,33(1):17-27
Chromium-reducible sulfur (CRS) distillations are intended to recover only reduced inorganic sulfur compounds (RIS) including elemental sulfur. However, the quantitative recovery of elemental sulfur is not ensured in common CRS-distillations. The new method presented here was designed to remedy this deficiency. An increase in ethanol concentration assured the quantitative recovery of elemental sulfur in various forms and, in addition, all other RIS-compounds were quantitatively recovered. Furthermore, the selectivity of the procedure was improved by an additional filtration step to eliminate zinc particles from the Cr(II)-solution. Thus, the recovery of sulfates and organic sulfur compounds was significantly decreased by a factor of up to 35, depending on the compound analysed. Exhaustive testing with a variety of pure phases, rock and soil samples demonstrated the precision and accuracy of the new method. The new protocol eliminated the constraints of previous procedures. The improved distillation efficiency for elemental sulfur ensured the quantitative recovery of all RIS-compounds in a single-step distillation. 相似文献
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17.
《Chemie der Erde / Geochemistry》2017,77(1):147-157
The study was carried out on the Sulejów dam reservoir (Central Poland). Water and sediment samples were collected between February and October 2006. Sulfur compounds in the sediment were chemically extracted and subjected to isotopic analysis.Large variability of SO42− concentration in the water column (from 10.3 to 36.2 mg/dm3) and the isotopic composition of sulfur (δ34S from 2.1 to 5.4‰) was observed. The main identified sources of SO42− were watercourses, surface runoff, and phosphorus fertilizers.Both oxidized sulfur species (SO42−) and its reduced forms were found in sediments. Particular sulfur forms were characterized by large variations in both, concentrations and the isotopic composition of sulfur. SO42− in the sediment and in the water column had different genesis. Bacterial oxidation of organic sulfur and its binding in SO42− were observed in the sediment. Under reducing conditions, oxidized and organic sulfur is converted to H2S which reacted with Fe or other metallic ions leading to metal sulfide precipitation. Monosulfides were shown to have a very low concentration, ranging up to 0.07 mg/g of sediment. The transformation of elemental sulfur from sulfides through their chemical oxidation occurred in the sediment. 相似文献
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硫磺渣是硫磺矿区主要的矿业固废,其随意堆放可产生一系列的环境地质问题,并对山水林田湖草等自然资源、环境及人的健康构成较大危害。滇东北地区长期以硫铁矿为原料、以煤炭为燃料,土法炼硫生产硫磺,导致巨量硫磺渣堆积,产生了严重的环境地质问题。本文针对该地区镇雄县硫磺矿区,调查了小硫磺生产形成硫磺渣的规模和特征,梳理了该硫磺矿区主要环境地质问题及其对当地生态环境的影响,认为目前镇雄硫磺矿区存在的环境污染、自然资源破坏及可能形成的矿渣性泥石流等环境地质现状与过去40多年的小硫磺生产密切相关。基于以上认识,强调应结合矿业固废无害化、减量化和资源化技术政策,从资源回收利用、生态环境恢复、地质灾害防治和文化遗产保护方面探讨和提出镇雄硫磺矿区矿渣治理和生态修复的新理念和新对策。 相似文献
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硫的来源对于了解铁氧化物铜金矿床的形成过程和成因具有重要的意义。文中统计了拉拉铁氧化物铜金矿硫化物的 硫同位素数据,并结合地质特征和矿相学研究,分析和讨论了硫的同位素组成特征和硫的来源。结果表明,拉拉铜金矿硫 同位素组成变化较大(不考虑一个异常样品,δ34S 值极差达到 14.9‰),表明成矿硫来源的多样性;其中,黄铁矿 δ34S 值范 围为 -1.4‰ ~4.9‰(平均 1.8‰),黄铜矿的 δ34S 值范围为 -5.9‰ ~9‰(平均 1.5‰)。结合硫化物的生成机制分析,并与其 他典型矿床硫同位素数据对比,表明海水沉淀的蒸发岩是黄铁矿和黄铜矿的重要硫来源,但也不能排除岩浆硫的贡献。目 前没有证据支持变质作用减少拉拉矿区硫化物的硫同位素组成差异。 相似文献