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1.
Geochronology and Genesis of the Tiegelongnan Porphyry Cu(Au) Deposit in Tibet: Evidence from U–Pb,Re–Os Dating and Hf,S, and H–O Isotopes 
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下载免费PDF全文 Bin Lin Ju‐Xing Tang Yu‐Chuan Chen Yang Song Greg Hall Qin Wang Chao Yang Xiang Fang Ji‐lin Duan Huan‐Huan Yang Zhi‐Bo Liu Yi‐Yun Wang Jun Feng 《Resource Geology》2017,67(1):1-21
The Tiegelongnan Cu (Au) deposit is the largest copper deposit newly discovered in the Bangong–Nujiang metallogenic belt. The deposit has a clear alteration zoning consisting of, from core to margin, potassic to propylitic, superimposed by phyllic and advanced argillic alteration. The shallow part of the deposit consists of a high sulphidation‐state overprint, mainly comprising disseminated pyrite and Cu–S minerals such as bornite, covellite, digenite, and enargite. At depth porphyry‐type mineralization mainly comprises disseminated chalcopyrite, bornite, pyrite, and a minor vein molybdenite. Mineralization is disseminated and associated with veins contained within the porphyry intrusions and their surrounding rocks. The zircon U–Pb ages of the mineralized diorite porphyry and granodiorite porphyry are 123.1 ± 1.7 Ma (2σ) and 121.5 ± 1.5 Ma (2σ), respectively. The molybdenite Re–Os age is 121.2 ± 1.2 Ma, suggesting that mineralization was closely associated with magmatism. Andesite lava (zircon U–Pb age of 111.7 ± 1.6 Ma, 2σ) overlies the ore‐bodies and is the product of post‐mineralization volcanic activity that played a critical role in preserving the ore‐bodies. Values of ?4.6 ‰ to + 0.8 ‰ δ34S for the metal sulfides (mean ? 1.55 ‰) suggest that S mainly has a deep magmatic source. The H and O isotopic composition is (δD = ?87 ‰ to ?64 ‰; δ18OH2O = 5.5 ‰ to 9.0 ‰), indicating that the ore‐forming fluids are mostly magmatic‐hydrothermal, possibly mixed with a small amount of meteoric water. The zircon εHf(t) of the diorite porphyry is 3.7 to 8.3, and the granodiorite porphyry is 1.8 to 7.5. Molybdenite has a high Re from 382.2 × 10?6 to 1600 × 10?6. Re and Hf isotope composition show that Tiegelongnan has some mantle source, maybe the juvenile lower crust from crust–mantle mixed source. Metallogenesis of the Tiegelongnan giant porphyry system was associated with intermediate to acidic magma in the Early Cretaceous (~120 Ma). The magma provenance of the Tiegelongnan deposit has some mantle‐derived composition, possibly mixed with the crust‐derived materials. 相似文献
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The Sin Quyen-Lung Po district is an important Cu metallogenic province in Vietnam, but there are few temporal and genetic constraints on deposits from this belt. Suoi Thau is one of the representative Cu deposits associated with granitic intrusion. The deposit consists of ore bodies in altered granite or along the contact zone between granite and Proterozoic meta-sedimentary rocks. The Cu-bearing intrusion is sub-alkaline I-type granite. It has a zircon U-Pb age of ~776 Ma, and has subduction-related geochemical signatures. Geochemical analysis reveals that the intrusion may be formed by melting of mafic lower crust in a subduction regime. Three stages of alteration and mineralization are identified in the Suoi Thau deposit, i.e., potassic alteration; silicification and Cu mineralization; and phyllic alteration. Two-phase aqueous fluid inclusions in quartz from silicification stage show wide ranges of homogenization temperatures(140–383℃) and salinities(4.18wt%–19.13wt%). The high temperature and high salinity natures of some inclusions are consistent with a magmatic derivation of the fluids, which is also supported by the H-O-S isotopes. Fluids in quartz have δD values of –41.9‰ to –68.8‰. The fluids in isotopic equilibrium with quartz have δ~(18)O values ranging from 7.9‰ to 9.2‰. These values are just plotted in the compositional field of magmatichydrothermal fluids in the δD_(water) versus δ~(18)O_(water) diagram. Sulfide minerals have relatively uniform δ~(34)S values from 1.84‰ to 3.57‰, which is supportive of a magmatic derivation of sulfur. The fluid inclusions with relatively low temperatures and salinities most probably represent variably cooled magmatic-hydrothermal fluids. The magmatic derivation of fluids and the close spatial relationship between Cu ore bodies and intrusion suggest that the Cu mineralization most likely had a genetic association with granite. The Suoi Thau deposit, together with other deposits in the region, may define a Neoproterozoic subduction-related ore-forming belt. 相似文献
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Zircon U–Pb,Molybdenite Re–Os and K‐feldspar 40Ar/39Ar Dating of the Bolong Porphyry Cu–Au Deposit,Tibet, China 下载免费PDF全文
下载免费PDF全文 Xiangping Zhu Guangming Li Huaan Chen Dongfang Ma Hanxiao Huang 《Resource Geology》2015,65(2):122-135
The Bolong porphyry Cu–Au deposit is a newly discovered deposit in the central Tibetan Plateau, and is ranked as the second largest copper deposit discovered to date in the Bangong‐Nujiang metallogenic belt in China. Three granodiorite porphyry phases occur within the Bolong porphyry Cu–Au deposit. Phyllic alteration is widespread on the surface of the deposit, and potassic alteration occurs at depth, associated with granodiorite porphyries. The copper and gold mineralization is clearly related to the potassic and phyllic alteration. Multiple chronometers were applied to constrain the timing of magmatic–hydrothermal activity at the Bolong deposit. Zircon U–Pb geochronology reveals that the granodiorite porphyry phases were emplaced at ca. 120 Ma. Re–Os data of four molybdenite samples from quartz–molybednite veinlets yielded an isochron age of 119.4 ± 1.3 Ma. The plateau age of hydrothermal K‐feldspar from the potassic alteration zone, analyzed by 40Ar/39Ar dating, is 118.3 ± 0.6 Ma, with a similar reverse isochron age of 118.5 ± 0.7 Ma. Therefore, the magmatic–hydrothermal activity occurred at ca. 120–118 Ma, which is similar in age to the neighboring Duobuza porphyry copper deposit. The period of 120–118 Ma is therefore important for the development of porphyry Cu–Au mineralization in the central Tibetan Plateau, and these porphyry deposits were formed during the final stages of the northward subduction of the Neo‐Tethys Ocean. 相似文献
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The unidirectional solidification textures (UST) quartz is generally thought to form from fluids exsolved from shallow intrusions and/or magma chambers, but such an idea is still poorly constrained from the evidence of stable isotopes. In this study, we report for the first time the δ18O of quartz that shows UST from the Qulong Cu–Mo and the Yechangping Mo porphyry deposits in China. The analysis results show that the UST quartz samples from the Qulong deposit have δ18O values ranging from +6.2 ‰ to +7.6 ‰, which are similar to that of quartz phenocrysts (+6.7 ‰ to +7.8 ‰). In contrast, the UST quartz samples from the Yechangping porphyry Mo deposit yield a high δ18O value (+10.0 ‰). The δ18Owater value of Yechangping UST quartz (+8.5 ‰) is also higher than that of Qulong (+4.6 ‰ to +5.8 ‰). Hydrothermal biotite from potassic alteration and sericite from early phyllic alteration at Qulong have similar δ18O values to UST quartz, suggesting the involvement of magmatic fluids during this stage of deposit evolution. 相似文献
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Lei CHEN Kezhang QIN Jinxiang LI Bo XIAO Guangming LI Junxing ZHAO Xin FAN 《Resource Geology》2012,62(1):42-62
The Nuri Cu‐W‐Mo deposit is located in the southern subzone of the Cenozoic Gangdese Cu‐Mo metallogenic belt. The intrusive rocks exposed in the Nuri ore district consist of quartz diorite, granodiorite, monzogranite, granite porphyry, quartz diorite porphyrite and granodiorite porphyry, all of which intrude in the Cretaceous strata of the Bima Group. Owing to the intense metasomatism and hydrothermal alteration, carbonate rocks of the Bima Group form stratiform skarn and hornfels. The mineralization at the Nuri deposit is dominated by skarn, quartz vein and porphyry type. Ore minerals are chalcopyrite, pyrite, molybdenite, scheelite, bornite and tetrahedrite, etc. The oxidized orebodies contain malachite and covellite on the surface. The mineralization of the Nuri deposit is divided into skarn stage, retrograde stage, oxide stage, quartz‐polymetallic sulfide stage and quartz‐carbonate stage. Detailed petrographic observation on the fluid inclusions in garnet, scheelite and quartz from the different stages shows that there are four types of primary fluid inclusions: two‐phase aqueous inclusions, daughter mineral‐bearing multiphase inclusions, CO2‐rich inclusions and single‐phase inclusions. The homogenization temperature of the fluid inclusions are 280°C–386°C (skarn stage), 200°C–340°C (oxide stage), 140°C–375°C (quartz‐polymetallic sulfide stage) and 160°C–280°C (quartz‐carbonate stage), showing a temperature decreasing trend from the skarn stage to the quartz‐carbonate stage. The salinity of the corresponding stages are 2.9%–49.7 wt% (NaCl) equiv., 2.1%–7.2 wt% (NaCl) equiv., 2.6%–55.8 wt% (NaCl) equiv. and 1.2%–15.3 wt% (NaCl) equiv., respectively. The analyses of CO2‐rich inclusions suggest that the ore‐forming pressures are 22.1 M Pa–50.4 M Pa, corresponding to the depth of 0.9 km–2.2 km. The Laser Raman spectrum of the inclusions shows the fluid compositions are dominated in H2O, with some CO2 and very little CH4, N2, etc. δD values of garnet are between ?114.4‰ and ?108.7‰ and δ18OH2O between 5.9‰ and 6.7‰; δD of scheelite range from ?103.2‰ to ?101.29‰ and δ18OH2O values between 2.17‰ and 4.09‰; δD of quartz between ?110.2‰ and ?92.5‰ and δ18OH2O between ?3.5‰ and 4.3‰. The results indicate that the fluid came from a deep magmatic hydrothermal system, and the proportion of meteoric water increased during the migration of original fluid. The δ34S values of sulfides, concentrated in a rage between ?0.32‰ to 2.5‰, show that the sulfur has a homogeneous source with characteristics of magmatic sulfur. The characters of fluid inclusions, combined with hydrogen‐oxygen and sulfur isotopes data, show that the ore‐forming fluids of the Nuri deposit formed by a relatively high temperature, high salinity fluid originated from magma, which mixed with low temperature, low salinity meteoric water during the evolution. The fluid flow through wall carbonate rocks resulted in the formation of layered skarn and generated CO2 or other gases. During the reaction, the ore‐forming fluid boiled and produced fractures when the pressure exceeded the overburden pressure. Themeteoric water mixed with the ore‐forming fluid along the fractures. The boiling changed the pressure and temperature, oxygen fugacity, physical and chemical conditions of the whole mineralization system. The escape of CO2 from the fluid by boiling resulted in scheelite precipitation. The fluid mixing and boiling reduced the solubility of metal sulfides and led the precipitation of chalcopyrite, molybdenite, pyrite and other sulfide. 相似文献
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The skarn‐type tungsten deposit of the Date‐Nagai mine is genetically related to the granodiorite batholith of the Iidateyama body. Skarn is developed along the contact between pelitic hornfels and marble that remains as a small roof pendant body directly above the granodiorite batholith. Zonal arrangement of minerals is observed in skarn. The zonation consists of wollastonite, garnet, garnet‐epidote, and vesuvianite‐garnet zones, from marble to hornfels. Sheelite is included in garnet, garnet‐epidote, and vesuvianite‐garnet zones. The oxygen isotope values of skarn minerals were obtained as δ18O = 4.2–7.7‰ for garnet, 5.9–6.9‰ for vesuvianite, ?0.3–3.4‰ for scheelite, 6.0–10.9‰ for quartz, and 8.2‰ for muscovite. The temperature of skarn‐formation was calculated from oxygen isotopic values of scheelite‐quartz pairs to be 288°C. Calculated oxygen isotope values of fluid responsible for skarn minerals were 6.1–9.5‰ for garnet, 1.2–4.8‰ for scheelite, ?1.3‐3.6‰ for quartz, and 4.5‰ for muscovite. Garnet precipitated from the fluids of different δ18O values from scheelite, quartz, and muscovite. These δ18O values suggest that the origin of fluid responsible for garnet was magmatic water, while evidence for the presence of a meteoric component in the fluids responsible for middle to later stages minerals was confirmed. 相似文献
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德兴铜厂斑岩铜(钼金)矿床蚀变-矿化系统流体演化:H-O同位素制约 总被引：2，自引：0，他引：2
江西铜厂斑岩铜(钼金)矿床是德兴斑岩矿集区最大的矿床.文章根据铜厂矿床发育的钾硅酸盐化、绢英岩化、青磐岩化蚀变组合特征,和已厘定的铜厂矿床脉体类型,选取代表不同蚀变矿化阶段的石英、黑云母、绢云母及绿泥石等,进行单矿物的H、O同位素测试.石英和黑云母单矿物O同位素,与石英、黑云母平衡流体的δ 18O 值和δD值联合示踪结果显示,铜厂矿床早期A脉(不规则疙瘩状A1脉、石英-黑云母A2脉和石英-磁铁矿A4脉)和中期B脉(矿物组合为石英-黄铁矿+黄铜矿±辉钼矿±斑铜矿)形成时,成矿热液均为岩浆流体来源,但B脉可能混入了少量大气降水;晚期低温D脉和碳酸岩脉(180～200℃)的成矿热液全部为大气降水来源.斑晶黑云母平衡水的δ 18O和δD值变化范围较大表明,黑云母形成时的热液系统主要为岩浆水,局部受区域变质水和大气降水的混染,也可能与少量黑云母斑晶受到后期绿泥石化、水云母化蚀变有关.绿泥石蚀变主要由岩浆流体作用形成,但混入了一些大气降水,导致其δ 18O值少量降低.绢云母平衡的水的δ18O值和δD值(4.6‰和-19.4‰)表明,绢云母是大气降水与千枚岩共同作用的结果.总体来说,铜厂矿床钾硅酸盐化、绿泥石化蚀变,以及钾硅酸盐化阶段形成的A脉和B脉,均由岩浆流体作用引起,大气降水在绿泥石化阶段进入蚀变-矿化系统,而绢云母化、晚期低温D脉和碳酸盐脉均是大气降水作用的产物. 相似文献
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Fluid Inclusions,C–H–O–S Isotope and Geochronology of the Bujinhei Pb–Zn Deposit in the Southern Great Xing'an Range of Northeast China: Implication for Ore Genesis 下载免费PDF全文
下载免费PDF全文 Xuebing Zhang Keyong Wang Lijuan Fu Miao Zhang Yassa Konare Dawei Peng Wenyan Cai 《Resource Geology》2017,67(2):207-227
The Bujinhei Pb–Zn deposit is located in the southern Great Xing'an Range metallogenic belt. It is a representative medium‐ to high‐temperature hydrothermal vein type deposit controlled by fractures, and orebodies hosted in the Permian Shoushangou Formation. The hydrothermal mineralization is classified into three stages: pyrite ± arsenopyrite–quartz (Stage 1), polymetallic sulfide–quartz (Stage 2), and polymetallic sulfide–calcite (Stage 3). Fluid inclusion petrography, laser Raman analyses and microthermometry indicate that the liquid‐rich aqueous inclusions (L) and vapor‐rich CO2 ± CH4–H2O inclusions (C) occur in the Stage 1 and as medium‐ to high‐ temperature and low‐ to medium‐salinity NaCl–H2O–CO2–CH4 hydrothermal fluids. The liquid‐rich (L) and rare vapor‐rich CO2 ± CH4–H2O inclusions (C) occur in the Stage 2 with medium‐temperature and low‐salinity NaCl–H2O ± CO2 ± CH4 hydrothermal fluids. The exclusively liquid‐rich (L) fluid inclusions are observed in the Stage 3, and the hydrothermal fluid belongs to medium‐temperature and low‐salinity NaCl–H2O hydrothermal fluids. The results of hydrogen and oxygen isotope analyses indicate that ore‐forming fluids were initially derived from the magmatic water and mixed with local meteoric water in the late stage (δ18OH2O‐SMOW = 6.0 to 2.2‰, δDSMOW = ?103 to ?134‰). The carbon isotope compositions (?18.4‰ to ?26.5‰) indicate that the carbon in the fluid was derived from the surrounding strata. The sulfur isotope compositions (5.7 to 15.2‰) indicate that the ore sulfur was also primarily derived from the strata. The ore vein No. 1 occurs in fractures and approximately parallel to the rhyolite porphyry; orebodies have a close spatial and temporal relationship with the rhyolite porphyry. The rhyolite porphyry yielded a crystallization age of 122.9 ± 2.4 Ma, indicating that the Bujinhei deposit may be related to the Early Cretaceous magmatic event. Geochemical analyses reveal that the Bujinhei rhyolite porphyry is high in K2O and peraluminous, and derived from an acidic liquid as a result of strong interaction with hydrothermal fluid during the late magmatic stage; it is similar to A2‐type granites, and formed in a backarc extensional environment. These results indicate that the Bujinhei Pb–Zn deposit was a vein type system that formed in Early Cretaceous and influenced by the Paleo‐Pacific tectonic system. Bujinhei deposit is a representative hydrothermal vein type deposit on the genetic types, and occurs on the western slope of the southern Great Xing'an Range. The ore‐forming fluids were medium‐ to high‐temperature and low‐to medium‐salinity NaCl–H2O–CO2–CH4 hydrothermal fluids, which became medium‐temperature and low‐salinity NaCl–H2O hydrothermal fluids in later stages, and came from magmatic water and mixed with meteoric water, whereas the ore‐forming materials were mainly derived from the surrounding strata. The LA–ICP–MS zircon U–Pb dating indicates that the Bujinhei deposit formed at the period of late Early Cretaceous, potentially in a backarc extensional environment influenced by the Paleo‐Pacific tectonic system. 相似文献
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德兴斑岩铜矿成矿热液来源及其演化——花岗闪长斑岩的氧同位素制约 总被引：8，自引：0，他引：8
作者研究了德兴铜厂花岗闪长斑岩的氧同位素组成特征在垂直方向上的变化规律,及蚀变作用对花岗闪长斑岩全岩和单矿物氧同位素组成的影响。结果表明,从地表到深部,花岗闪长斑岩全岩和长石单矿物的δ＾１８Ｏ值总体上有逐渐降低的趋势,反映花岗闪长斑岩受到已演化的大气降水水－岩氧同位素交换作用的影响。水－岩交换作用对花岗闪长斑岩氧同位素组成的影响在浅部和深部是不同的,这主要受控于水－岩交换温度和交换水的初始氧同位素组成等因素。石英的氧同位素组成及变化特征不同于全岩和长石,其值与岩石的蚀变作用有关从花岗闪长斑岩的氧同位煮组成及其变化规律可以推论,由大气降水演化为德兴斑岩铜矿成矿热液是可能的。 相似文献
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德兴朱砂红斑岩铜矿热液蚀变作用及元素地球化学迁移规律 总被引：12，自引：7，他引：5
德兴铜矿是中国华南地区重要的大型斑岩铜矿,由朱砂红、铜厂和富家坞3个矿床组成。在系统的钻孔样岩相观察基础上,本文把德兴朱砂红花岗闪长斑岩划分为3种类型蚀变岩(钾化-黑云母化蚀变岩、绿泥石化蚀变岩、石英-绢(白)云母化蚀变岩),其主要标志性蚀变矿物依次为:钾长石(黑云母)→绿泥石→石英+绢(白)云母,且热液蚀变程度依次增强。以Al2O3作为不活动组分,通过Isocon分析法表明:随着热液蚀变作用的持续进行,蚀变程度的逐渐增强,主量元素(P2O5)行为较稳定,Na2O、Sr元素大量活化迁出;高场强元素Hf、Th、U、V、Co、Nb、Ta等表现为弱活动性或不活动性;成矿元素Cu、Pb、W显示出大量带入,表明热液流体和成矿流体可能属于同一流体系统。稀土元素均发生一定程度的活化迁移,其中绿泥石化蚀变岩的LREE、HREE均较原岩亏损,而石英-绢(白)云母化花岗闪长斑岩的LREE、HREE富集/亏损情况因样品而异,相对增量/减量变化幅度较大。各类蚀变花岗闪长斑岩球粒陨石化配分模式表现较一致,均为轻稀土相对于重稀土富集的右倾分布,极弱Eu负异常,曲线左陡右平缓,尾部轻微上翘,形似铲状,反映岩浆源区角闪石的分离结晶作用。蚀变花岗闪长斑岩的Y/Ho比值与球粒陨石的Y/Ho比值基本一致,表明Y-Ho在热液蚀变过程中未发生明显分离。弱蚀变花岗闪长斑岩具有较高Sr/Y比值、La/Sm比值以及中等Sm/Yb比值,暗示源区残留相主要为角闪石±石榴子石。 相似文献
13.
德兴铜厂斑岩型铜金矿床热液演化过程 总被引：13，自引：2，他引：11
德兴铜矿是中国东部大陆环境最具代表性的大型斑岩铜矿,由朱砂红、铜厂及富家坞三大矿床组成,其中的铜厂矿体以富金而别具特色.在前人研究基础上,本文通过系统的野外观测、详细的岩芯编录和全面的岩相学研究,厘定了铜厂矿床的脉体类型和形成顺序,系统地开展了各类脉体的流体包裹体研究,查明了成矿流体的演化过程,再塑了岩浆-热液矿化过程.初步识别出德兴矿床3组脉体类型,分别记录了三个不同阶段的蚀变-成矿过程:早期A脉分为4类,形成于成矿早期斑岩尚未固结时,伴有大规模的钾化和黑云母化甚至磁铁矿化;中期B脉可分为7类,形成于斑岩体固结后的大规模裂隙事件发育期,B脉石英呈梳状对称生长、黄铁矿以中心线生长;后期D脉共有3类,发育于成矿晚期,系雨水大量加入和硫化物大量淀积产物.观察发现,所有A、B及D脉沉淀过程中,均伴随大量的岩浆流体出溶、热液蚀变、流体挥发等热液活动、各脉均捕获了同体系内富含的热液流体.详细显微镜鉴定表明,各类脉体的脉石矿物石英内发育的大部分包裹体与世界典型斑岩铜矿床的矿化特征相似,从成矿早期A脉到成矿晚期D脉包裹体的类型发生如下变化:早期以LVH(含单子晶或多子晶包裹体发育,包裹体中还见有金属硫化物)+富气相包裹体为主→中期以含单子晶包裹体+富气相包裹体为主,以及含有少量富液相包裹体→成矿晚期,以富液相包裹体+少量富气相包裹体.包裹体显微测温结果总体上指示了温度、压力及热液成分在各类脉体的形成过程的变化规律,从早期到晚期温度和盐度逐渐降低,热液成矿作用明显经历三个阶段:早期岩浆未完全固结,温度达到800～600℃以上,压力较高(140～50MPa),发生强烈的钾硅酸盐化;中期,由于岩浆冷凝结晶,岩体顶部围岩裂隙发育,静岩压力向静水压力发生转换,温度下降到450～550℃,压力陡然从55～40MPa下降至20MPa(B脉);而D脉形成时,发生大规模绿泥石-水云母化,温度下降至350～375℃,压力完全降低至20MPa以下;最后,与成矿作用无关的热液活动了两次,峰值温度分别是320～300℃和180～200℃,形成了无矿碳酸盐脉、石英脉及黑云母. 在成矿过程中,成矿热液也从形成A/B脉时以岩浆热液为主,转变为形成D脉时以雨水、地下水为主.与世界典型斑岩型铜矿床相比,德兴斑岩铜矿床的蚀变-矿化系统基本一致,都由强硅酸盐蚀变带--青磐岩蚀变带--泥岩蚀变带等构成,在不同的蚀变阶段形成了具有特色的不规则形状A脉、脉石矿物梳状对称的B脉及粗颗粒大脉型D脉.德兴铜厂铜金矿各成矿阶段内主要成矿流体特征及其演化过程基本类似于世界典型斑岩矿床.但是,也存在不同之处,在铜厂铜金矿的A、B及D脉都发育了少量CO_2包裹体,表明德兴铜厂成矿过程中CO_2参与成矿作用,世界其它斑岩型矿床或没有报道发育 CO_2 包裹体(杨志明等,2008),或者仅在其中某个阶段发现了少量CO_2包裹体(Harris et al., 2004).CO_2包裹体参与成矿是否有特殊指示意义,须进一步的工作才能得出正确的结论. 相似文献
14.
DING Hui GE Wensheng DONG Lianhui ZHANG Liangliang CHEN Xiaodong LIU Yan NIE Junjie 《《地质学报》英文版》2018,92(3):1100-1122
The Weiquan Ag-polymetallic deposit is located on the southern margin of the Central Asian Orogenic Belt and in the western segment of the Aqishan-Yamansu arc belt in East Tianshan,northwestern China. Its orebodies, controlled by faults, occur in the lower Carboniferous volcanosedimentary rocks of the Yamansu Formation as irregular veins and lenses. Four stages of mineralization have been recognized on the basis of mineral assemblages, ore fabrics, and crosscutting relationships among the ore veins. Stage I is the skarn stage(garnet + pyroxene), Stage Ⅱ is the retrograde alteration stage(epidote + chlorite + magnetite ± hematite 士 actinolite ± quartz),Stage Ⅲ is the sulfide stage(Ag and Bi minerals + pyrite + chalcopyrite + galena + sphalerite + quartz ± calcite ± tetrahedrite),and Stage IV is the carbonate stage(quartz + calcite ± pyrite). Skarnization,silicification, carbonatization,epidotization,chloritization, sericitization, and actinolitization are the principal types of hydrothermal alteration. LAICP-MS U-Pb dating yielded ages of 326.5±4.5 and 298.5±1.5 Ma for zircons from the tuff and diorite porphyry, respectively. Given that the tuff is wall rock and that the orebodies are cut by a late diorite porphyry dike, the ages of the tuff and the diorite porphyry provide lower and upper time limits on the age of ore formation. The δ~(13)C values of the calcite samples range from-2.5‰ to 2.3‰, the δ~(18)O_(H2 O) and δD_(VSMOW) values of the sulfide stage(Stage Ⅲ) vary from 1.1‰ to 5.2‰ and-111.7‰ to-66.1‰, respectively,and the δ~(13)C, δ~(18)O_(H2 O) and δD_(V-SMOW) values of calcite in one Stage IV sample are 1.5‰,-0.3‰, and-115.6‰, respectively. Carbon, hydrogen, and oxygen isotopic compositions indicate that the ore-forming fluids evolved gradually from magmatic to meteoric sources. The δ~(34)S_(V-CDT) values of the sulfides have a large range from-6.9‰ to 1.4‰, with an average of-2.2‰, indicating a magmatic source, possibly with sedimentary contributions. The ~(206)Pb/~(204)Pb, ~(207)Pb/~(204)Pb, and ~(208)Pb/~(204)Pb ratios of the sulfides are 17.9848-18.2785,15.5188-15.6536, and 37.8125-38.4650, respectively, and one whole-rock sample at Weiquan yields~(206)Pb/~(204)Pb,~(207)Pb/~(204)Pb, and ~(208)Pb/~(204)Pb ratios of 18.2060, 15.5674, and 38.0511,respectively. Lead isotopic systems suggest that the ore-forming materials of the Weiquan deposit were derived from a mixed source involving mantle and crustal components. Based on geological features, zircon U-Pb dating, and C-H-OS-Pb isotopic data, it can be concluded that the Weiquan polymetallic deposit is a skarn type that formed in a tectonic setting spanning a period from subduction to post-collision. The ore materials were sourced from magmatic ore-forming fluids that mixed with components derived from host rocks during their ascent, and a gradual mixing with meteoric water took place in the later stages. 相似文献
15.
《Resource Geology》2018,68(1):1-21
The Daheishan Mo deposit of the Lesser Xing'an–Zhangguangcai Range metallogenic belt in northeast China is a super‐large molybdenum deposit with Mo reserves of 1.09 Mt. The Mo mineralization occurs mainly in a granodiorite porphyry. Zircon SIMS U–Pb dating yields a crystallization age of 168.3 ± 1.4 Ma for the granodiorite porphyry. Molybdenite Re–Os dating indicates that Mo mineralization occurred at 169.2 ± 1.2 Ma. These geochronological data indicate that these magmatic and hydrothermal activities occurred during the Middle Jurassic. The granodiorite porphyry can be classified as high‐K calc‐alkaline series, and the rare earth elements (REE) are characterized by a significant fractionation between light REE (LREE) and heavy REE (HREE) with slightly positive Eu anomalies (Eu/Eu* = 1.08–1.12). Large ion lithophile elements (e.g., Rb, U, K, and Pb) are enriched, whereas high field strength elements (e.g., Nb, Ta, Ti, HREEs, and Yb) are strongly depleted. The granodiorite porphyry is also characterized by initial strontium isotope ratios (87Sr/86Sr)i of 0.70460–0.70482 and magmatic zircon δ18O values of 5.2–6.5 ‰ that are similar to those of the mantle. Zircon ɛHf(t) and whole‐rock ε Nd(t) values range from 5.6 to 9.9 and 0.8 to 1.1, respectively. The two‐stage Nd model ages (TDM2) are in the range of 868–894 Ma, similar to Hf model ages, indicating that the parent magma has a uniform source and primarily originated from a juvenile crustal source. Combined with the regional geological history, geochemistry of the Daheishan granodiorite porphyry, and new isotopic age data, we propose that the formation of the Daheishan porphyry Mo deposit is likely related to the subduction of the Paleo‐Pacific Plate. 相似文献
16.
The study presents copper (Cu) isotope data of mineral separates of chalcopyrite from four drill core samples in the Miocene Dabu porphyry Cu-Mo deposit formed in a post-collisional setting in the Gangdese porphyry copper belt, southern Tibet. Copper isotope values in hypogene chalcopyrite range from –1.48‰ to +1.12‰, displaying a large variation of up to 2.60‰, which demonstrates Cu isotope fractionation at high-temperature during hydrothermal evolution. The majority of measured chalcopyrite isotopic compositions show a gradual increasing trend from –1.48‰ to +1.12‰ with the increase of drilling depth from 130m to 483m, as the alteration assemblages change from potassic to phyllic. Similarly, the other δ65Cu values (δ65Cu = ((65Cu/63Cu)sample/(65Cu/63Cu)standard − 1) × 1000) of the chalcopyrite show a gradual increasing trend from −1.48‰ to +0.59‰ with the decrease of drilling depth from 130 m to 57 m, as the alteration assemblages change from potassic, phyllic, through argillic to relatively fresh. These observations suggest a genetic link between Cu isotope variation and silicate alteration assemblages formed at different temperatures, indicative of a Rayleigh precipitation process resulting in the large variation of δ65Cu values at Dabu. In general, samples closest to the center of hydrothermal system dominated by high-temperature potassic alteration are isotopically lighter, whereas samples dominated by low-temperature phyllic alteration peripheral to the center are isotopically heavier. The predicted flow pathways of hydrothermal fluids are from No. 0 to No. 3 exploration line, and the lightest δ65Cu values are the most proximal to the hydrothermal source. Finally, we propose that the northwest side of the No. 0 exploration line has high potential for hosting undiscovered orebodies. The pattern of Cu isotope variation in conjunction with the features of silicate alteration in porphyry system can be used to trace the hydrothermal flow direction and to guide mineral exploration. 相似文献
17.
《Chemie der Erde / Geochemistry》2023,83(2):125956
The Iju Cu porphyry is located in the NW part of the Kerman Magmatic Copper Belt (KMCB). It is related to a ~ 9 Ma granodiorite porphyry intrusion, with three main stages of hydrothermal activity. The homogenization temperatures for the fluid inclusions are in the ranges of 200–494 °C, and their salinities vary from 4.0 to 42.8 wt% NaCl equiv., which are typical magmatic-hydrothermal fluids. The δ34S values of sulfides range from −0.4 to +3.2 ‰ (V-CDT), and the δ34S values of anhydrite samples range from +11.6 to +16.8 ‰. The δ34S values of sulfides show a narrow range, implying a homogeneous sulfur source. The oxygen isotopic composition of hydrothermal water in equilibrium with quartz samples ranges from +3.4 to +6.0 ‰ (V-SMOW) consistent with the hydrothermal fluids having a magmatic signature, but diluted with meteoric waters in the main mineralizing stage. The most important factors responsible for metal precipitation in the Iju porphyry deposit are fluid boiling, oxygen fugacity decrease and cooling followed by dilution with meteoric water. The primary fluids of the Iju Cu deposit are characterized by relatively high temperature and moderate salinity, and are CO2-rich, indicating a typical post-collisional porphyry system. 相似文献
18.
《International Geology Review》2012,54(12):1353-1368
Copper and gold mineralization in the Maher-Abad area, eastern Iran, is closely related to multiple episodes of emplacement of a late Eocene granodiorite into a quartz-monzonitic stock and andesitic volcaniclastic rocks. Hypogene and supergene porphyry Cu–Au mineralization occurred within the porphyritic granodiorite and quartz-monzonite host rocks extensively altered into dominantly potassic, propylitic, phyllic, and argillic assemblages. Temperature and pressure estimates using the plagioclase–hornblende thermometer and Al-in-hornblende barometer indicate that the granodiorite intruded at 758 ± 10°C and 1.4 ± 0.2 kbar. Biotites from the alteration zones have more variable AlIV than those in the fresh granodiorite, but nearly all are close to the ideal phlogopite composition. Biotite compositions display an increase in Al2O3, FeO, TiO2, and Cl, but a decrease in SiO2 and F, from the porphyritic granodiorite and potassic to the transitional phyllic alteration zones. Biotite from the potassic zone (X phl?=?0.63–0.67) possesses a moderate F content (0.53 to 0.82 wt.%) that is significantly higher than that in the phyllic zone (0.22 to 0.38 wt.%), exhibiting a positive correlation with X Mg and negative correlation with Cl. With a decrease in the temperature, log (fH2O/fHF) and log (fH2O/fHCl) values calculated for fluids equilibrated with biotite increase progressively from the granodiorite through the potassic to the phyllic zones, whereas log (fHF/fHCl) shifts towards more negative values. Fugacity ratio trends in the Maher-Abad porphyry copper deposit are quite similar to those of other porphyry copper systems. The decrease in halogen content of hydrothermal fluids towards outer parts of the deposits reflects an increase in the degree of mixing between magmatic fluid and meteoric water. 相似文献
19.
TANG Yanwen LI Xiaofeng XIE Yuling HUANG Cheng WEI Hao CAI Jiali YIN Yifan QIN Chaojian LIU Rong 《《地质学报》英文版》2015,89(3):766-782
The Tongcun Mo(Cu) deposit in Kaihua city of Zhejiang Province,eastern China,occurs in and adjacent to the Songjiazhuang granodiorite porphyry and is a medium-sized and important porphyry type ore deposit.Two irregular Mo(Cu) orebodies consist of various types of hydrothermal veinlets.Intensive hydrothermal alteration contains skarnization,chloritization,carbonatization,silicification and sericitization.Based on mineral assemblages and crosscutting relationships,the oreforming processes are divided into five stages,i.e.,the early stage of garnet + epidote ± chlorite associated with skarnization and K-feldspar + quartz ± molybdenite veins associated with potassicsilicic alteration,the quartz-sulfides stage of quartz + molybdenite ± chalcopyrite ± pyrite veins,the carbonatization stage of calcite veinlets or stockworks,the sericite + chalcopyrite ± pyrite stage,and the late calcite + quartz stage.Only the quartz-bearing samples in the early stage and in the quartzsulfides stage are suitable for fluid inclusions(FIs) study.Four types of FIs were observed,including1) CO_2-CH_4 single phase FIs,2) CO_2-bearing two- or three-phase FIs,3) Aqueous two-phase FIs,and4) Aqueous single phase FIs.FIs of the early stages are predominantly CO_2- and CH_4-rich FIs of the CO_2-CH4-H_2O-NaCl system,whereas minerals in the quartz-sulfides stage contain CO_2-rich FIs of the CO_2-H_2O-NaCl system and liquid-rich FIs of the H_2O-NaCl system.For the CO_2-CH_4 single phase FIs of the early mineralization stage,the homogenization temperatures of the CO_2 phase range from 15.4 ℃ to 25.3 ℃(to liquid),and the fluid density varies from 0.7 g/cm~3 to 0.8 g/cm~3;for two- or three-phase FIs of the CO_2-CH_4-H_2O-NaCl system,the homogenization temperatures,salinities and densities range from 312℃ to 412℃,7.7 wt%NaCl eqv.to 10.9 wt%NaCl eqv.,and 0.9 g/cm~3 to 1.0 g/cm~3,respectively.For CO_2-H_2O-NaCI two- or threephase FIs of the quartz-sulfides stage,the homogenization temperatures and salinities range from255℃ to 418℃,4.8 wt%NaCl eqv.to 12.4 wt%NaCl eqv.,respectively;for H_2O-NaCl two-phase FIs,the homogenization temperatures range from 230 ℃ to 368 ℃,salinities from 11.7 wt%NaCl eqv.to16.9 wt%NaCl eqv.,and densities from 0.7 g/cm~3 to 1.0 g/cm~3.Microthermometric measurements and Laser Raman spectroscopy analyses indicate that CO_2 and CH_4 contents and reducibility(indicated by the presence of CH_4) of the fluid inclusions trapped in quartz-sulfides stage minerals are lower than those in the early stage.Twelve molybdenite separates yield a Re-Os isochron age of 163 ± 2.4 Ma,which is consistent with the emplacement age of the Tongcun,Songjiazhuang,Dayutang and Huangbaikeng granodiorite porphyries.The S18OSMow values of fluids calculated from quartz of the quartz-sulfides stage range from 5.6‰ to 8.6‰,and the JDSMOw values of fluid inclusions in quartz of this stage range from-71.8‰ to-88.9‰,indicating a primary magmatic fluid source.534SV-cdt values of sulfides range from+1.6‰ to +3.8‰,which indicate that the sulfur in the ores was sourced from magmatic origins.Phase separation is inferred to have occurred from the early stage to the quartz-sulfides stage and resulted in ore mineral precipitation.The characteristics of alteration and mineralization,fluid inclusion,sulfur and hydrogen-oxygen isotope data,and molybdenite Re-Os ages all suggest that the Tongcun Mo(Cu) deposit is likely to be a reduced porphyry Mo(Cu) deposit associated with the granodiorite porphyry in the Tongcun area. 相似文献
20.
Geordie Mark Damien R. W. Foster Peter J. Pollard Patrick J. Williams Justin Tolman Michael Darvall Kevin L. Blake 《地学学报》2004,16(2):54-61
Sodic–calcic alteration is common in mineralized hydrothermal systems, yet the relative importance of igneous vs. basinal fluid sources remains controversial. One of the most extensive volumes of sodic–calcic rocks occurs near Cloncurry, NW Queensland, and was formed by overlapping hydrothermal systems that were active synchronously with emplacement of mid‐crustal batholithic granitoids (c. 1.55–1.50 Ga). Altered rocks contain albite–oligoclase, actinolite, diopside, titanite and magnetite. Alteration was localized by: (A) composite veins and breccias containing crystallized magma intimately intergrown with hydrothermal precipitates; (B) intrusions that host setting A veins and breccias; and (C) extensive breccia and vein systems linked to regional fault systems. Isotope analyses of actinolites in settings A and B indicate calculated δ18OH2O (+8.2 to +10.6‰) and variably depleted δDH2O (?130 to ?54‰) compared with typical magmatic fluids, whereas those from setting C typically indicate calculated δ18OH2O (+8.0 to +12.8‰) and δDH2O (?29 to ?99‰). The lowest δDH2O values are interpreted as representing residual fluids after significant (> 90%) open‐system magmatic degassing. Overall the stable isotope, field, geochronological and geobarometric data suggest that these sodic–calcic alteration systems were formed by the episodic incursion of magmatic fluids that underwent minor isotopic modification as a result of varying degrees of interaction with country rocks. 相似文献