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1.
云南羊拉铜矿床矿物组成、地球化学特征及其地质意义   总被引：3，自引：0，他引：3  
云南羊拉铜矿床位于金沙江构造带中部,是三江地区一个十分典型的大型铜矿床。羊拉铜矿床的金属矿物为黄铜矿、黄铁矿、磁黄铁矿、方铅矿、自然铋、辉铋矿、毒砂、辉砷钴矿、辉钼矿等,根据金属矿物的共生组合,推测羊拉铜矿床为中高温热液矿床。羊拉铜矿床与羊拉花岗闪长岩体具有密切的成因联系,通过对羊拉铜矿床铜矿石稀土元素、微量元素的分布特征和羊拉花岗闪长岩的对比及S、Pb同位素组成的研究,表明成矿物质主要来源于地幔,部分来源于岩浆。早二叠世晚期金沙江洋盆向西俯冲形成了一系列逆断层。同时,金沙江洋盆向西低角度俯冲导致下地壳部分熔融,引发大规模的火山岩浆作用。在晚三叠世早期,构造背景由挤压环境到伸展环境的转折期,这些逆断层具有张性的特点,为后期的成矿热液提供了有利的容矿构造。持续上升的岩浆为地幔楔内的成矿流体提供了通道,岩浆内的部分成矿流体进入羊拉花岗闪长岩体附近的逆断层富集成矿。  相似文献   

2.
The Yangla copper deposit, located in western Yunnan Province, China, is a typical giant, newly started mining copper deposit with an estimated Cu reserves of about 1,200,000 tons. The deposit is spatially and temporally associated with the Linong granodiorite, which is rich in SiO2 (SiO2=58.25 wt%–69.84 wt%) and alkalis (Na2O+K2O=5.98 wt%–8.34 wt%), indicating an association with shoshonitic series to high-K calc-alkaline series granites, and shows low contents of TiO2 (0.35 wt%–0.48 wt%), MgO (1.51 wt%–1.72 wt%), and Al2O3 (13.38 wt%–19.75 wt%). The δ34S values of sulfides of the main ore stage from copper ores vary range from ?4.2‰ to ?0.9‰, indicating a much greater contribution from the mantle to the ore-forming fluids. The δ34S values of the late ore stage is ?9.8‰, indicating enrichment of biogenic sulfur which may derive from the crustal hydrothermal fluid. The 208Pb/204Pb, 207Pb/204Pb and 206Pb/204Pb of sulfides of the main ore stage from copper ores range within 38.66–38.73, 15.71–15.74 and 18.35–19.04, respectively, implying that the Pb was derived from the mantle, with the crustal component, probably representing mixtures of mantle lead and crustal lead. Sulfide of the late ore stage in their Pb isotopic composition, 208Pb/204Pb= 38.69, 207Pb/204Pb=15.70, 206Pb/204Pb=18.35, implying that the Pb was derived from the crust. The Linong granodiorite is syn-collisional, produced by partial melting of thickened lower crust, which was triggered by the westward subduction of the Jinshajiang Oceanic plate. During a transition in geodynamic setting from collision-related compression to extension, gently dipping ductile shear zones (related to subduction) were transformed to brittle shear zones, consisting of a series of thrust faults in the Jinshajiang tectonic belt. The tensional thrust faults would have been a favorable environment for ore-forming fluids. The ascending magma provided a channel for the ore-forming fluid from the mantle wedge. After the magma arrived at the base of the early-stage Linong granodiorite, the platy granodiorite at the base of the body would have shielded the late-stage magma from the fluid. The magma would have cooled slowly, and some of the ore-forming fluid in the magma would have entered the gently dipping thrust faults near the Linong granodiorite, resulting in mineralization.  相似文献   

3.
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   

4.
鲁春铜铅锌矿床位于中咱-中甸板块和昌都-思茅板块之间的金沙江构造带中部,矿体长约3 km,厚度在1.06～16.35 m之间。其赋矿围岩为火山沉积岩系,容矿构造为印支期逆断层。鲁春铜铅锌矿床矿石中硫化物的δ34S值变化于3.5‰～6.8‰之间,硫化物的206Pb/204Pb比值为18.554～18.656,207Pb/204Pb比值为15.662～15.752,208Pb/204Pb比值为38.801～39.009。石英流体包裹体的HO182δO值变化范围为2.74‰～1.25‰,δDV-SMOW变化范围为107‰～123‰。鲁春铜铅锌矿床的硫铅氢氧同位素分析结果表明,该矿床成矿物质来源于地幔,部分来源于岩浆,在成矿流体上升过程中,有壳源物质的加入。早二叠世晚期金沙江洋盆向西俯冲形成了一系列逆断层,同时导致下地壳部分熔融,引发大规模的火山岩浆作用。在晚三叠世早期,构造背景由挤压环境到伸展环境的转折期,这些逆断层具有张性的特点,为后期的成矿热液提供了有利的容矿构造。上升的岩浆为地幔楔内的成矿流体提供了通道。岩浆内的部分成矿流体进入白茫雪山花岗闪长岩体附近的逆断层富集成矿。  相似文献   

5.
The genesis of mineralized systems across the Mountain Freegold area, in the Dawson Range Cu–Au?±?Mo Belt of the Tintina Au province was constrained using Pb and stable isotope compositions and Ar–Ar and Re–Os geochronology. Pb isotope compositions of sulfides span a wide compositional range (206Pb/204Pb, 18.669–19.861; 208Pb/204Pb, 38.400–39.238) that overlaps the compositions of the spatially associated igneous rocks, thus indicating a magmatic origin for Pb and probably the other metals. Sulfur isotopic compositions of sulfide minerals are broadly similar and their δ34S (Vienna-Canyon Diablo Troilite (V-CDT)) values range from ?1.4 to 3.6 ‰ consistent with the magmatic range, with the exception of stibnite from a Au–Sb–quartz vein, which has δ34S values between ?8.1 and ?3.1 ‰. The δ34S values of sulfates coexisting with sulfide are between 11.2 and 14.2 ‰; whereas, those from the weathering zone range from 3.7 to 4.3 ‰, indicating supergene sulfates derived from oxidation of hypogene sulfides. The δ13C (Vienna Peedee Belemnite (VPDB)) values of carbonate range from ?4.9 to 1.1 ‰ and are higher than magmatic values. The δ18O (V-SMOW) values of magmatic quartz phenocrysts and magmatic least-altered rocks vary between 6.2 and 10.1 ‰ and between 5.0 and 10.1 ‰, respectively, whereas altered magmatic rocks and hydrothermal minerals (quartz and magnetite) are relatively 18O-depleted (4.2 to 7.9 ‰ and ?6.3 to 1.5 ‰, respectively). Hydrogen isotope compositions of both least-altered and altered igneous rock samples are D-depleted (from ?133 to ?161 ‰ Vienna-Standard Mean Ocean Water (V-SMOW)), consistent with differential magma degassing and/or post-crystallization exchange between the rocks and meteoric ground water. Zircon from a chlorite-altered dike has a U–Pb crystallization age of 108.7?±?0.4 Ma; whereas, the same sample yielded a whole-rock Ar–Ar plateau age of 76.25?±?0.53 Ma. Likewise, molybdenite Re–Os model ages range from 75.8 to 78.2 Ma, indicating the mineralizing events are genetically related to Late Cretaceous volcano-plutonic intrusions in the area. The molybdenite Re–Os ages difference between the nearby Nucleus (75.9?±?0.3 to 76.2?±?0.3 Ma) and Revenue (77.9?±?0.3 to 78.2?±?0.3 Ma) mineral occurrences suggests an episodic mineralized system with two pulses of hydrothermal fluids separated by at least 2 Ma. This, in combination with geological features suggest the Nucleus deposit represents the apical and younger portion of the Revenue–Nucleus magmatic-hydrothermal system and may suggest an evolution from the porphyry to the epithermal environments.  相似文献   

6.
Hydrothermal iron ores at Divri?i, east Central Anatolia, are contained in two orebodies, the magnetite-rich A-kafa and the limonitic B-kafa (resources of 133.8 Mt with 56% Fe and 0.5% Cu). The magnetite ores are hosted in serpentinites of the Divri?i ophiolite at the contact with plutons of the Murmano complex. Hydrothermal biotite from the Divri?i A-kafa yield identical weighted mean plateau ages of 73.75?±?0.62 and 74.34?±?0.83 Ma (2σ). This biotite represents a late alteration phase, and its age is a minimum age for the magnetite ore. Similar magnetite ores occur at Hasançelebi and Karakuz, south of Divri?i. There, the iron ores are hosted in volcanic or subvolcanic rocks, respectively, and are associated with a voluminous scapolite ± amphibole ± biotite alteration. At Hasançelebi, biotite is intergrown with parts of the magnetite, and both minerals formed coevally. The weighted mean plateau ages of hydrothermal biotite of 73.43?±?0.41 and 74.92?±?0.39 Ma (2σ), therefore, represent mineralization ages. Hydrothermal biotite from a vein cutting the scapolitized host rocks south of the Hasançelebi prospect has a weighted mean plateau age of 73.12?±?0.75 Ma (2σ). This age, together with the two biotite ages from the Hasançelebi ores, constrains the minimum age of the volcanic host rocks, syenitic porphyry dikes therein, and the scapolite alteration affecting both rock types. Pyrite and calcite also represent late hydrothermal stages in all of these magnetite deposits. The sulfur isotope composition of pyrite between 11.5 and 17.4‰ δ34S(VCDT) points towards a non-magmatic sulfur source of probably evaporitic origin. Calcite from the Divri?i deposit has δ18O(VSMOV) values between +15.1 and +26.5‰ and δ13C(VPDB) values between ?2.5 and +2.0‰, which are compatible with an involvement of modified marine evaporitic fluids during the late hydrothermal stages, assuming calcite formation temperatures of about 300°C. The presence of evaporite-derived brines also during the early stages is corroborated by the pre-magnetite scapolite alteration at Divri?i, and Hasançelebi-Karakuz, and with paleogeographic and paleoclimatic reconstructions. The data are compatible with a previously proposed genetic model for the Divri?i deposit in which hydrothermal fluids leach and redistribute iron from ophiolitic rocks concomitant with the cooling of the nearby plutons.  相似文献   

7.
The Yinan gold deposit in the Luxi area of Shandong Province in northeastern China is a skarn-type ore deposit. In this article, we present results from sulphur, lead, carbon–oxygen, and helium–argon isotope chemistry to characterize the ore genesis and source features. We also present rhenium–osmium ages from molybdenite to evaluate the timing of ore formation. The δ34S values of pyrite from the ore deposit range from 0.7‰ to 5.60‰ with a mean at 2.70‰, close to mantle and meteorite sulphur. Among Pb isotopes, 206Pb/204Pb values range from 18.375 to 18.436, 207Pb/204Pb values from 15.694 to 15.8, and 208Pb/204Pb values from 38.747 to 39.067. The δ13C values of calcite associated with the ores range from ?0.2‰ to ?0.5‰ and their δ18O values show variation from 9.4‰ to 12.6‰, suggesting a mixed fluid source. The 3He/4He and 40Ar/36Ar ratios of fluids trapped in pyrite are in the range of 0.27–1.11 Ra and 439.4–826, respectively, with calculated proportion of the mantle-derived He ranging from 3.25% to 14.03% and atmosphere argon ranging from 35.8% to 67.3%. The data suggest that the ore-forming fluids were derived from the crust and were mixed with a distinct contribution of mantle helium. The Re and Os values vary from 32 × 10?6 to 93.02 × 10?6 and from 0.01 × 10?9 to 0.34 × 10?9, respectively. The model ages of molybdenite range from 126.96 ± 1.82 Ma to 129.49 ± 2.04 Ma, with a weighted mean age of 128.08 ± 0.75 Ma and isochron age of 130.3 ± 3 Ma. These ages are close to the age of the associated quartz diorite porphyrite pluton, suggesting a close relationship between Cretaceous magmatism and metallogeny in NE China. A comparison of the Yinan gold deposit in the Luxi area with those of the Jiaodong area shows that the contrast in metallogenic features between the two are linked with the tectonic and geodynamic history.  相似文献   

8.
ABSTRACT

The Suyunhe porphyry Mo deposit, located in the West Junggar terrane, is the largest molybdenum deposit found in Xinjiang to date, with a proven reserve of 0.57 Mt. The Suyunhe deposit is associated with Early Permian granitic rocks, which emplaced into the volcano-sedimentary sequences of the Middle Devonian Barluk Formation. Four metallogenic stages are identified in this study. Stage I is marked by the quartz-magnetite-K-feldspar±biotite±pyrite±molybdenite veins, which mainly occurred in the intensively potassic alternation zone and were formed at high temperature (>481°C), high salinity (58.6?65.18 wt.%), and relatively high oxygen fugacity conditions with a fluid system of NaCl-H2O-CO2. Stage II is the main metallogenic stage and develops numerous quartz-molybdenite±pyrite veins associated with muscovite–chlorite alteration, which were formed by immiscible fluids at medium-high temperature (210?427°C), medium-high salinity (43.36?49.90 wt.%), and relatively low oxygen fugacity conditions with the fluid system of NaCl-H2O-CO2-CH4-C2H6. After the main Mo-mineralization, quartz-polymetallic sulphides veins associated with quartz–sericite alteration were formed by fluids at medium-low temperature, low-salinity conditions with the fluid system of NaCl-H2O-CO2 in stage III. The following quartz-polymetallic sulphide veins are quartz-calcite±pyrite veins associated with calcite alteration, which were formed by fluids at low temperature and low-salinity conditions with a fluid system of NaCl-H2O in stage IV.

The δ18O‰ values indicate that the ore fluids of stages I and II are dominated by magmatic water, whereas stages III and IV are dominated by meteoric water. A wide range of δ34S‰ values (?7.1 to 3.4‰) of sulphides between stages I and II indicates that increasing the reducibility plays an important role in molybdenum mineralization. The δ13CCH4 values suggest that CH4 of the ore fluids mainly results from the assimilation–contamination of carbonaceous country rocks, and partly derives from magma. However, the δ13CCO2 values suggest that CO2 of the ore fluids mainly originates from magma, and minor derives from wall-rocks as well as meteoric water.  相似文献   

9.
The Arapuçandere Pb–Zn–Cu ore body is a typical vein-type lead–zinc deposit of the Biga Peninsula, and is currently being mined for lead and zinc. In the study area, Permian–Triassic metamorphic rocks, Triassic metaclastic and metabasic rocks, Oligocene–Miocene granitoids, Miocene volcanic rocks, and Quaternary terrigenous sediments crop out. The ore deposits developed as Pb–Zn–Cu-bearing veins along faults in Triassic metasandstone and metadiabase. Microscopic studies reveal that the veins contain galena, sphalerite, chalcopyrite, pyrite, marcasite, covellite, and specular hematite as ore minerals, and quartz, calcite, and barite as gangue minerals. Analysed sulphur-isotope compositions (δ34SVCDT) of galena, sphalerite, and chalcopyrite range from ? 5.9 to ? 1.9‰ (average ? 3.4‰), from ? 5.5 to ? 1.7‰ (average ? 4.2 ‰), and from ? 3.5 to ? 0.9‰ (average ? 2.6‰), respectively; that of H2S in the hydrothermal fluid was in the calculated range of ? 5.8 to +0.1‰ (average ? 2.5‰). These isotopic values suggest that magmatic sulphur dominates in sulphides, mixed with minor, isotopically light sulphur. Because no contemporaneous magmatic activity is associated with mineralization, it may be assumed that sulphur was leached from the surrounding Triassic units, mainly from metabasic, partly from metaclastic rocks. Lead-isotope studies indicate a model age of 114–63 Ma for the lead reservoir, in accord with possible sulphur-bearing local source rocks. Thus, the sulphur and lead deposited in the studied ore veins were probably leached from Triassic metabasic and metaclastic rocks some time during the Early Cretaceous to the Palaeocene.  相似文献   

10.
The Yangla Cu deposit is the largest Cu skarn deposit in the Jinshajiang tectonic belt. Based on the detailed observation of crosscutting relationships, three mineralization stages (i.e., pre-ore, ore and supergene) have been identified in the Yangla deposit. The pre-ore stage is dominated by prograde skarn. The ore stage is characterized by the precipitation of hydrous silicate minerals, Fe-oxides, Fe-Cu-Mo-sulfides, quartz and calcite, whose mineral assemblages were formed in the early and late sub-ore stages. The early sub-ore stage is marked by retrograde alteration with the deposition of hydrous silicate minerals (e.g., actinolite, epidote and chlorite), Fe-oxides, abundant Fe-Cu-Mo-sulfides, quartz and minor calcite. Whilst, the late sub-ore stage, associated with silicic and carbonate alteration, is represented by widespread thick quartz or calcite veins with disseminated pyrite, chalcopyrite, galena and sphalerite. We present new carbon-oxygen (C-O) isotopic compositions of the ore-hosting marble and hydrothermal calcite of this deposit. The hydrothermal calcite in the Yangla deposit was precipitated from both the early and late sub-ore stages. Calcite I from the early sub-ore stage is anhedral, and occurs as spot in the skarn or locally replaces the skarn minerals. Calcite II from the late sub-ore stage is distinguished by being coarse-grained, subhedral to euhedral and its occurrence in thick veins. Calcite I contains lower δ13CPDB (−7.0‰ to −5.0‰) and δ18OSMOW (7.2‰ to 12.7‰) than Calcite II (δ13CPDB = −4.5‰ to −2.3‰; δ18OSMOW = 10.7‰ to 19.4‰). In the δ13CPDB vs. δ18OSMOW diagram, the Calcite I and Calcite II data fall close to the igneous carbonatite field and between the fields of igneous carbonatite and marine carbonates, respectively. This suggests a dominantly magmatic origin for the early sub-ore fluids, and there might have been increasing carbonate wall rock involvement towards the late sub-ore stage. The ore-hosting marble (δ13CPDB = −4.8‰ to −0.3‰; δ18OSMOW = 10.2‰ to 23.9‰) also shows a positive δ13CPDB vs. δ18OSMOW correlation, which is interpreted to reflect the decreasing alteration intensity during the interactions between the hydrothermal fluids and ore-hosting carbonates. Simulated calculation suggests that both the Calcite I and Calcite II precipitated at 350 °C to 250 °C and 250 °C to 150 °C, respectively. We proposed that CO2 degassing and water/rock interactions were likely the two major processes that precipitated the calcite and led to the observed C-O isotopic features of the Yangla Cu deposit.  相似文献   

11.
The Maoniuping REE deposit, located about 22 km to the southwest of Mianning, Sichuan Province, is the second largest light REE deposit in China, subsequent to the Bayan Obo Fe-Nb-REE deposit in the Inner Mongolia Autonomous Region. Tectonically, it is located in the transitional zone between the Panxi rift and the Longmenshan-Jinpingshan orogenic zone. It is a carbonatite vein-type deposit hosted in alkaline complex rocks. The bastnaesite-barite, bastnaesite-calcite, and bastnaesite-microcline lodes are the main three types of REE ore lodes. Among these, the first lode is distributed most extensively and its REE mineralization is the strongest. Theδ34Sv-CDT values of the barites in the ore of the deposit vary in a narrow range of +5.0 to +5.1‰in the bastnaesite-calcite lode and +3.3 to +5.9‰in the bastnaesite-barite lode, showing the isotopic characteristics of magma-derived sulfur. Theδ13Cv-PDB values and theδ518OV-SMOW values in the bastnaesite-calcite lode range from -3.9 to -6.9‰and from +7.3 to +9.7‰, respectively, which fall into the range of "primary carbonatites", showing that carbon and oxygen in the ores of the Maoniuping deposit were derived mainly from a deep source. Theδ13Cv-PDB values of fluid inclusions vary from -3.0 to -5.6‰, with -3.0 to -4.0‰in the bastnaesite-calcite lode and -3.0 to -5.6‰in the bastnaesite-barite lode, which show characteristics of mantle-derived carbon. TheδDv-SMOW values of fluid inclusions range from -57 to -88‰, with -63 to -86‰in the bastnaesite-calcite lode and -57 to -88‰in the bastnaesite-barite lode, which show characteristics of mantle-derived hydrogen. Theδ18OH2OV-SMOW values vary from +7.4 to +8.6‰in the bastnaesite calcite lode, and +6.7 to +7.8‰in the bastnaesite-barite lode, almost overlapping the range of +5.5 to +9.5‰for magmatic water. The 4He content, R/Ra ratios are (13.95 to 119.58×10-6 (cm3/g)STP and 0.02 to 0.11, respectively, and 40Ar/36Ar is 313±1 to 437±2. Considering the 4He increase caused by high contents of radioactive elements, a mantle-derived fluid probably exists in the inclusions in the fluorite, calcite and bastnaesite samples. The Maoniuping deposit and its associated carbonatite-alkaline complex were formed in 40.3 to 12.2 Ma according to K-Ar and U-Pb data. All these data suggest that large quantities of mantle fluids were involved in the metallogenic process of the Maoniuping REE deposit through a fault system.  相似文献   

12.
The Haobugao deposit, located in the southern segment of the Great Xing'an Range, is a famous skarn‐related Pb‐Zn‐(Cu)‐(Fe) deposit in northern China. The results of our fluid inclusion research indicate that garnets of the early stage (I skarn stage) contain three types of fluid inclusions (consistent with the Mesozoic granites): vapor‐rich inclusions (type LV, with VH2O/(VH2O + LH2O) < 50 vol %, and the majority are 5–25 vol %), liquid‐rich two‐phase aqueous inclusions (type VL, with VH2O/(VH2O + LH2O) > 50 vol %, the majority are 60–80 vol %), and halite‐bearing multiphase inclusions (type SL). These different types of fluid inclusions are totally homogenized at similar temperatures (around 320–420°C), indicating that the ore‐forming fluids of the early mineralization stage may belong to a boiling fluid system. The hydrothermal fluids of the middle mineralization stage (II, magnetite‐quartz) are characterized by liquid‐rich two‐phase aqueous inclusions (type VL, homogenization temperatures of 309–439°C and salinities of 9.5–14.9 wt % NaCl eqv.) that coexist with vapor‐rich inclusions (type LV, homogenization temperatures of 284–365°C and salinities of 5.2–10.4 wt % NaCl eqv.). Minerals of the late mineralization stage (III sulfide‐quartz stage and IV sulfide‐calcite stage) only contain liquid‐rich aqueous inclusions (type VL). These inclusions are totally homogenized at temperatures of 145–240°C, and the calculated salinities range from 2.0 to 12.6 wt % NaCl eqv. Therefore, the ore‐forming fluids of the late stage are NaCl‐H2O‐type hydrothermal solutions of low to medium temperature and low salinity. The δD values and calculated δ18OSMOW values of ore‐forming fluids of the deposit are in the range of ?4.8 to 2.65‰ and ?127.3‰ to ?144.1‰, respectively, indicating that ore‐forming fluids of the Haobugao deposit originated from the mixing of magmatic fluid and meteoric water. The S‐Pb isotopic compositions of sulfides indicate that the ore‐forming materials are mainly derived from underlying magma. Zircon grains from the mineralization‐related granite in the mining area yield a weighted 206Pb/238U mean age of 144.8 ±0.8 Ma, which is consistent with a molybdenite Re‐Os model age (140.3 ±3.4 Ma). Therefore, the Haobugao deposit formed in the Early Cretaceous, and it is the product of a magmatic hydrothermal system.  相似文献   

13.
The Maevatanana gold deposit in Madagascar is hosted by Archean metamorphic rocks in quartz–sulfide veins that are structurally controlled by NNW–SSE trending shear zones. Fluid inclusion data show that the trapping conditions in quartz range from 0.87 to 2.58 kbar at temperatures of 269–362 °C. Laser Raman spectroscopy confirms that these inclusions consist of CO2, SO2, and H2O. The δ34S values of the pyrites range from 1.7‰ to 3.6‰, with an average of 2.25‰, supporting a magmatic origin. Noble gases (He, Ne, Ar, Ke, Xe) are chemically inert, thus will not be involved in chemical reactions during geological processes. Also due to the low concentration of He in the atmosphere and the low solubility of He in aqueous fluids, the atmosphere-derived He is unlikely to significantly affect He abundances and isotopic ratios of crustal fluids, ensures that He production should have the typical crust 3He/4He ratios. The 3He/4He ratios of fluid inclusions in pyrite from the deposit range from 0.06 to 0.12 Ra, while the 40Ar/36Ar ratios range from 6631 to 11441. We infer that the ore-forming fluids could have been exsolved from a granitic magma. The oxygen and hydrogen isotope compositions of the ore-forming fluids (1.5‰ ≤ δ18OH2O ≤ 7.8‰; –72‰ ≤ δD ≤ –117‰) indicate they were derived from a granitic magma. Four pyrite samples from the gold deposit yield a precise Re–Os isochron age of 534 ± 13 Ma. Given that the post-collisional granites in northern and central Madagascar were derived by melting of sub-continental lithospheric mantle and formed between 537 and 522 Ma, we can state that the gold metallogenesis was coeval with the crystallization age of these parental magmas. These data could be accounted for the formation of the Maevatanana gold deposit. First, the shear zones hosting the deposit formed around 2.5 Ga, when the Madagascan micro-continental blocks collided with other continental blocks, triggering large-scale tectono-magmatic activity and forming NNW–SSE trending shear zones. The gold mineralization at Maevatanana is coeval with the crystallization age of the Cambrian post-collisional A-type granitoid plutons in northern and central Madagascar, implying that this deposit is associated with extensional collapse of the East African Orogen. This extension in turn induced asthenospheric upwelling, melting of sub-continental lithospheric mantle. These magmas underplated the lower crust, generating voluminous granitic magmas by partial melting of the lower crust. The mixing magma during tectono-thermal reactivation of the East African Orogen produced large volumes of volatiles that extracted gold from the granitic magma and produced Au–S complexes (e.g., Au(HSO3)2−). The shear zones, which were then placed under extensional collapse of the East African Orogen in the Cambrian, formed favorable pathways for the magmatic ore-forming fluids. These fluids then precipitated gold-sulfides that form the Maevatanana gold deposit.  相似文献   

14.
The Qianhe gold deposit in the Xiong’ershan area is located along the southern margin of the Archean-Paleoproterozoic North China Craton. The deposit consists of six orebodies that are hosted in Paleoproterozoic andesites to basaltic andesites and structurally controlled by roughly EW-trending faults. Individual orebodies comprise auriferous quartz veins and disseminated Au-bearing pyrite within hydrothermally altered rocks on both sides of, or close to, the veins. Ore-related hydrothermal alteration has produced various mixtures of K-feldspar, quartz, sericite, chlorite, epidote, carbonate, and sulfides. Pyrite is the most important ore mineral, associated with minor amounts of galena, sphalerite, and chalcopyrite. Other trace minerals include molybdenite, arsenopyrite, scheelite, rutile, xenotime, and parisite. Gold occurs mostly as native gold and electrum enclosed in pyrite or along microfractures of sulfides and quartz. Microthermometric measurements of primary inclusions in auriferous quartz suggest that gold and associated minerals were precipitated in the range of 160–305 °C from aqueous or carbonic-aqueous fluids with salinities of 6–22 wt% NaCl equiv. Samples of molybdenite coexisting with Au-bearing pyrite have Re–Os model ages of 134–135 Ma, whereas ore-related hydrothermal sericite separates yield 40Ar/39Ar plateau ages between 127 and 124 Ma. The Re–Os and 40Ar/39Ar ages are remarkably consistent with zircon U–Pb ages (134.5?±?1.5 and 127.2?±?1.4 Ma; 1σ) of the biotite monzogranite from the Heyu-intrusive complex and granitic dikes in and close to the Qianhe gold mine, indicating a close temporal and thus possibly genetic relationship between gold mineralization and granitic magmatism in the area. Fluid inclusion waters extracted from auriferous quartz have δD values of ?80 to ?72 ‰, whereas the calculated δ 18OH2O values range from 3.1 to 3.8 ‰. The hydrogen and oxygen isotopes from this study and previous work indicate that ore fluids were likely derived from degassing of magmas, with addition of minor amounts of meteoric water. Gold mineralization at Qianhe is temporarily coincident with pervasive bimodal magmatism, widespread fault-basin formation, and well development of metamorphic core complexes in the whole eastern North China Craton that have been interpreted as reflecting reactivation of the craton in the late Mesozoic after prolonged stabilization since its formation in the late Paleoproterozoic. It is therefore concluded that the Qianhe gold deposit formed as a result of this craton reactivation event.  相似文献   

15.
《International Geology Review》2012,54(12):1522-1549
ABSTRACT

The northern Lesser Xing’an Range in NE China hosts many gold deposits. However, genesis and tectonic background for the mineralization remain unclear. The newly discovered Yongxin gold deposit in this region provides a good example for understanding the related issues. Two economic orebodies have been recognized at Yongxin and they are mainly hosted in the hydrothermal breccias. Zircon U–Pb ages of granite porphyry and diorite porphyry are 119.3 ± 0.7 Ma and 119.9 ± 0.6 Ma, respectively. These data provide constraints to the upper limit of ore-forming age. The δ34S values of pyrite from orebodies range from 2.3‰ to 5.1‰. The 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb ratios of the pyrite are of 18.126–18.255, 15.492–15.537 and 37.880–38.019, respectively. The δ18OH2O and δD values of ore-forming fluids range from ?12.5‰ to 1.8‰ and from ?124.8‰ to ?102.1‰, respectively. The REE compositions of gold-bearing pyrite are similar to those of the volcanic rocks of the Longjiang formation, diorite porphyry and granite porphyry. The combined geological, geochronological and geochemical characteristics of the Yongxin gold deposit indicate that the ore-forming materials were likely sourced from the volcanic rocks of the Longjiang formation, diorite porphyry and granite porphyry, whereas the ore-forming fluids are dominated by meteoric water. The Yongxin gold deposit could be a product of the Early Cretaceous large-scale gold mineralization in northeast China which occurred in an extensional tectonic setting and were related to the rollback of the subducted Paleo-Pacific Oceanic Plate beneath the continental margin of northeast China.  相似文献   

16.
The Baiyangping Cu–Ag polymetallic ore district is located in the northern part of the Lanping–Simao foreland fold belt, which lies between the Jinshajiang–Ailaoshan and Lancangjiang faults in western Yunnan Province, China. The source of ore-forming fluids and materials within the eastern ore zone were investigated using fluid inclusion, rare earth element (REE), and isotopic (C, O, and S) analyses undertaken on sulfides, gangue minerals, wall rocks, and ores formed during the hydrothermal stage of mineralization. These analyses indicate: (1) The presence of five types of fluid inclusion, which contain various combinations of liquid (l) and vapor (v) phases at room temperature: (a) H2O (l), (b) H2O (l) + H2O (v), (c) H2O (v), (d) CmHn (v), and (e) H2O (l) + CO2 (l), sometimes with CO2 (v). These inclusions have salinities of 1.4–19.9 wt.% NaCl equivalents, with two modes at approximately 5–10 and 16–21 wt.% NaCl equivalent, and homogenization temperatures between 101 °C and 295 °C. Five components were identified in fluid inclusions using Raman microspectrometry: H2O, dolomite, calcite, CH4, and N2. (2) Calcite, dolomitized limestone, and dolomite contain total REE concentrations of 3.10–38.93 ppm, whereas wall rocks and ores contain REE concentrations of 1.21–196 ppm. Dolomitized limestone, dolomite, wall rock, and ore samples have similar chondrite-normalized REE patterns, with ores in the Huachangshan, Xiaquwu, and Dongzhiyan ore blocks having large negative δCe and δEu anomalies, which may be indicative of a change in redox conditions during fluid ascent, migration, and/or cooling. (3) δ34S values for sphalerite, galena, pyrite, and tetrahedrite sulfide samples range from −7.3‰ to 2.1‰, a wide range that indicates multiple sulfur sources. The basin contains numerous sources of S, and deriving S from a mixture of these sources could have yielded these near-zero values, either by mixing of S from different sources, or by changes in the geological conditions of seawater sulfate reduction to sulfur. (4) The C–O isotopic analyses yield δ13C values from ca. zero to −10‰, and a wider range of δ18O values from ca. +6 to +24‰, suggestive of mixing between mantle-derived magma and marine carbonate sources during the evolution of ore-forming fluids, although potential contributions from organic carbon and basinal brine sources should also be considered. These data indicate that ore-forming fluids were derived from a mixture of organism, basinal brine, and mantle-derived magma sources, and as such, the eastern ore zone of the Baiyangping polymetallic ore deposit should be classified as a “Lanping-type” ore deposit.  相似文献   

17.
The Martabe Au–Ag deposit, North Sumatra Province, Indonesia, is a high sulfidation epithermal deposit, which is hosted by Neogene sandstone, siltstone, volcanic breccia, and andesite to basaltic andesite of Angkola Formation. The deposit consists of six ore bodies that occurred as silicified massive ore (enargite–luzonite–pyrite–tetrahedrite–tellurides), quartz veins (tetrahedrite–galena–sphalerite–chalcopyrite), banded sulfide veins (pyrite–tetrahedrite–sphalerite–galena) and cavity filling. All ore bodies are controlled by N–S and NW–SE trending faults. The Barani and Horas ore bodies are located in the southeast of the Purnama ore body. Fluid inclusion microthermometry, and alunite‐pyrite and barite‐pyrite pairs sulfur isotopic geothermometry show slightly different formation temperatures among the ore bodies. Formation temperature and salinity of fluid inclusions of the Purnama ore body range from 200 to 260 C and from 6 to 8 wt.% NaCl equivalent, respectively. Formation temperature and salinity of fluid inclusions of the Barani ore body range from 200 to 220 °C and from 0 to 2.5 wt.% NaCl equivalent and those of the Horas ore body range from 240 to 275 °C and from 2 to 3 wt.% NaCl equivalent, respectively. The Barani and Horas ore bodies are less silicified and sulfides are less abundant than the Purnama ore body. A relationship between enthalpy and chloride content indicates mixing of hot saline fluids with cooler dilute fluids during the mineralization of each of the ore bodies. The δ18O values of quartz samples from the southeast ore bodies exhibit a wide range from +4.2 to +12.9‰ with an average value of +7.0‰. The δ18O values of H2O estimated from δ18O values of quartz, barite and calcite confirm the oxygen isotopic shift to near meteoric water trend, which support the incorporation of meteoric water. Salinity of the fluid inclusions decrease from >5 wt.% NaCl equivalent in the Purnama ore body to <3 wt.% NaCl equivalent in the Barani ore body, indicating different fluid systems during mineralization. The δ34S values of sulfide and sulfate in Purnama range from ? 4.2 to +5.5‰ and from +1.2 to +26.7‰, those in the Barani range from ? 4.3 to +26.4‰ and from +3.9 to +18.5‰ and those in the Horas ore body range from ? 11.8 to +3.5‰ and from +1.4 to +25.7‰, respectively. The δ34S of total bulk sulfur in southeastern ore bodies (Σδ34S) was estimated to be approximately +6‰. The estimated sulfur fugacity during formation of the Purnama and Horas ore bodies is relatively high. It was between 10?4.8 and 10?10.8 atm at 220 to 260 °C. Tellurium fugacity was between 10?7.8 and 10?9.5 atm at 260 °C and between 10?9 and 10?10.6 atm at 220 °C in the Purnama ore body. The Barani ore body was formed at lower fS2, lower than about 10?14 atm at 200 to 220 °C based on the presence of arsenopyrite and pyrrhotite in the early stage, and between 10?14 and 10?12 atm based on the existence of enargite and tennantite in the last stage. © 2016 The Society of Resource Geology  相似文献   

18.
The Badi copper deposit is located in Shangjiang town, Shangri-La County, Yunnan Province. Tectonically, it belongs to the Sanjiang Block. Vapor–liquid two-phase fluid inclusions, CO2-bearing fluid inclusions, and daughter-bearing inclusions were identified in sulfide-rich quartz veins. Microthermometric and Raman spectroscopy studies revealed their types of ore-forming fluids: (1) low-temperature, low-salinity fluid; (2) medium-temperature, low salinity CO2-bearing; and (3) high-temperature, Fe-rich, high sulfur fugacity. The δ18O values of chalcopyrite-bearing quartz ranged from 4.96‰ to 5.86‰, with an average of 5.40‰. The δD values of ore-forming fluid in equilibrium with the sulfide-bearing quartz were from ? 87‰ to ? 107‰, with an average of ? 97.86‰. These isotopic features indicate that the ore-forming fluid is a mixing fluid between magmatic fluid and meteoric water. The δ34S values of chalcopyrite ranged from 13.3‰ to 15.5‰, with an average of 14.3‰. Sulfur isotope values suggest that the sulfur in the deposit most likely derived from seawater. Various fluid inclusions coexisted in the samples; similar homogenization temperature to different phases suggests that the Badi fluid inclusions might have been captured under a boiling system. Fluid boiling caused by fault activity could be the main reason for the mineral precipitation in the Badi deposit.  相似文献   

19.
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   

20.
Peralkaline syenite and granite dykes cut the Straumsvola nepheline syenite pluton in Western Dronning Maud Land, Antarctica. The average peralkalinity index (PI?=?molecular Al/[Na?+?K]) of the dykes is 1.20 (n?=?29) and manifests itself in the presence of the Zr silicates eudialyte, dalyite and vlasovite, and the Na–Ti silicate, narsarsukite. The dykes appear to have intruded during slow cooling of the nepheline syenite pluton, and the petrogenetic relationship of the dykes and the pluton cannot be related to closed-system processes at low pressure, given the thermal divide that exists between silica-undersaturated and oversaturated magmas. Major and trace element variations in the dykes are consistent with a combination of fractional crystallization of parental peralkaline magma of quartz trachyte composition, and internal mineral segregation prior to final solidification. The distribution of accessory minerals is consistent with late-stage crystallization of isolated melt pockets. The dykes give an Rb–Sr isochron age of 171?±?4.4 Ma, with variable initial 87Sr/86Sr ratio (0.7075?±?0.0032), and have an average ε Nd of ? 12.0. Quartz phenocrysts have δ18O values of 8.4–9.2‰, which are generally in O-isotope equilibrium with bulk rock. Differences in the δ18O values of quartz and aegirine (average Δquartz?aegirine = 3.5‰) suggest aegirine formation temperatures around 500 °C, lower than expected for a felsic magma, but consistent with poikilitic aegirine that indicates subsolidus growth. The negative ε Nd (< ? 10) and magma δ18O values averaging 8.6‰ (assuming Δquartz?magma = 0.6‰) are inconsistent with a magma produced by closed-system fractional crystallization of a mantle-derived magma. By contrast, the nepheline syenite magma had mantle-like δ18O values and much less negative ε Nd (average ??3.1, n?=?3). The country rock has similar δ18O values to the granite dykes (average 8.0‰, n?=?108); this means that models for the petrogenesis of the granites by assimilation are unfeasible, unless an unexposed high-δ18O contaminant is invoked. Instead, it is proposed that the peralkaline syenite and granite dykes formed by partial melting of alkali-metasomatised gneiss that surrounds the nepheline syenite, followed by fractional crystallization.  相似文献   

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