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1.
《Journal of Asian Earth Sciences》2007,29(4-6):409-422
The Sar-Cheshmeh porphyry Cu–Mo deposit is located in Southwestern Iran (∼65 km southwest of Kerman City) and is associated with a composite Miocene stock, ranging in composition from diorite through granodiorite to quartz-monzonite. Field observations and petrographic studies demonstrate that the emplacement of the Sar-Cheshmeh stock took place in several pulses, each with associated hydrothermal activity. Molybdenum was concentrated at a very early stage in the evolution of the hydrothermal system and copper was concentrated later. Four main vein Groups have been identified: (I) quartz+molybdenite+anhydrite±K-feldspar with minor pyrite, chalcopyrite and bornite; (II) quartz+chalcopyrite+pyrite±molybdenite±calcite; (III) quartz+pyrite+calcite±chalcopyrite±anhydrite (gypsum)±molybdenite; (IV) quartz±calcite±gypsum±pyrite±dolomite. Early hydrothermal alteration produced a potassic assemblage (orthoclase-biotite) in the central part of the stock, propylitic alteration occurred in the peripheral parts of the stock, contemporaneously with potassic alteration, and phyllic alteration occurred later, overprinting earlier alteration. The early hydrothermal fluids are represented by high temperature (350–520 °C), high salinity (up to 61 wt% NaCl equivalent) liquid-rich fluid inclusions, and high temperature (340–570 °C), low-salinity, vapor-rich inclusions. These fluids are interpreted to represent an orthomagmatic fluid, which cooled episodically; the brines are interpreted to have caused potassic alteration and deposition of Group I and II quartz veins containing molybdenite and chalcopyrite. Propylitic alteration is attributed to a liquid-rich, lower temperature (220–310 °C), Ca-rich, evolved meteoric fluid. Influx of meteoric water into the central part of the system and mixing with magmatic fluid produced albitization at depth and shallow phyllic alteration. This influx also caused the dissolution of early-formed copper sulphides and the remobilization of Cu into the sericitic zone, the main zone of the copper deposition in Sar-Cheshmeh, where it was redeposited in response to a decrease in temperature. 相似文献
2.
The Darrehzar porphyry Cu-Mo deposit is located in Southwestern Iran (～70 km southwest of Kerman City). The porphyries occur as Tertiary quartz-monzonite stocks and dikes, ranging in composition from microdiorite to diorite and granodiorite. The Darrehzar stock is highly altered, and even in the outermost part of the intrusion, it is not possible to find completely fresh rock. Surface weathering was developing ferrous Fe-rich lithologic units in leached zone and concentrated copper minerals in supergene zone. Unlike eastern areas which do not account for deep faults, the supergene zone is well developed in western areas with maximum of 118 m thickness. Hydrothermal alteration and mineralization at Darrehzar are centered on the stock and were broadly synchronous with its emplacement. Early hydrothermal alteration was dominantly potassic and propylitic, and was followed by later phyllic and argillic alteration. The hydrothermal system involved both magmatic and meteoric water and boiled extensively. Copper mineralization was accompanied by both potassic and phyllic alteration. Four main vein groups have been identified: (I) quartz?+?pyrite?±?molybdenite?±?anhydrite?±?K-feldspar?±?chalcopyrite?±?bornite?±?Cu and Fe oxidic minerals (peripheral); (II) quartz?+?chalcopyrite?+?pyrite?+?molybdenite; (III) quartz?+?pyrite?±?calcite?±?chalcopyrite?±?anhydrite (gypsum); and (IV) quartz or calcite, gypsum or ± pyrite. Based on abundance, nature, and phases number observed at room temperature, three types of fluid inclusions are typically observed in these veins: (1) vapor-rich, (2) liquid-rich, and (3) multi-phase. Early hydrothermal alteration was caused by high temperature, high salinity orthomagmatic fluid and produced a potassic assemblage. Phyllitic alteration was caused by high salinity and lower temperature orthomagmatic fluid. Magmatic and meteoric water mixture was developed in the peripheral part of the stock and caused propylitic alteration which is attributed to a liquid-rich, lower temperature. 相似文献
3.
The Chah-Firuzeh porphyry copper deposit is located in 35 km north of Shahre Babak (Kerman province). It is associated with granodioriteic intrusive of Miocene age which intruded Eocene volcanosedimentary rocks. Copper mineralization was accompanied by both potassic and phyllic alteration. Field observations and petrographic studies demonstrate that the emplacement of Chah-Firuzeh pluton took place in several intrusive pulses, each with associated hydrothermal ore fluid formation that was also associated with hydrostatic pressure increasing respect to that of lithostatic pressure (and fracturing development-relative boiling) by circulated fluid. Copper is concentrated as a very early hydrothermal mineralized phase in the evolution of the hydrothermal system. Early hydrothermal alteration produced a potassic assemblage (orthoclase–biotite) in the central deep part of the stock. Alteration ore fluids could be classify into two groups of liquid-reach, containing solid phases, high temperature (390 to 500 °C) high salinity (more than 60 wt.% NaCl equiv.) and gas-rich, high temperature (311 to 570 °C), no solid phase and with low salinities. These magmatic source fluids illustrate sever boiling process and also are the responsible for the both potassic alteration, quartz group I and II veins and chalcopyrite deposition. Propylitic alteration occurred by the liquid-rich, low temperature (241 to 390 °C) and Ca-rich fluid with meteoric origin. Continuous decreasing temperature let the meteoric water diffusion into the system, mixed with magmatic fluids and descending the salinities down to the 1 wt.% NaCl equiv. and leaching the Cu from vein groups II and III by sever thermodynamic anarchies from potassic to the phyllic alteration zones. Phyllic alteration and copper leaching resulted from the inflow of oxidized and acidic meteoric waters with decreasing temperature of the system followed by the incursion of this fluid into and its convection in upper part of the system. A late episode of boiling occurred in the apical the phyllic zone, and was associated with significant copper deposition. Based on the field observation on sharp alteration and related mineralization, it is possible to conclude that all these procedures have been controlled by local faults that could be active even before the pluton injection. These faults and the new form ones (which have been formed after injection), could crash the hosted rocks, and act as physical dams to restrict and limit the mineralization in special strikes and zones within the Cah-Firuzeh ore deposit. 相似文献
4.
The Daraloo field is located in the southeast of Iran (Kerman province). It is associated with Oligomiocene diorite/granodiorite to quartz monzonite stocks. Copper mineralization is basically relevant to potassic and phyllic alteration zones. Petrographic and geologic studies imply that mineralization is restricted to two major parts locating in the center and east of district. The larger central mineralization has a northwest–southeast trend perpendicular to the smaller one. Hydrothermal ore fluid formation occurred in relatively deep levels thereafter faulting and fracturing provided appropriate conduits to ascend fluids through shallower depths. Early hydrothermal alteration produced a confined potassic assemblage in the central and eastern parts of the stock. Two main fluid inclusion groups in relationship with alteration ore fluids have been identified. They are liquid-rich inclusions containing solid phases, with high temperatures (257°C to 554°C) and high salinities (31 to 67 wt.% NaCl equiv.), and vapor-rich inclusions with high temperatures and low salinities without any solid phases. These magmatic source fluids are responsible for boiling and also potassic and phyllic alteration zone. They also resulted in the formation of quartz groups I and II veins and chalcopyrite deposition. Propylitic alteration is attributed to a Ca-rich meteoric fluid. Inclusions originated from this fluid are liquid-rich having low temperatures (161°C to 269°C) and low salinities (1 to 13 wt.% NaCl). Mixing descending meteoric water with magmatic fluids reduces considerably the salinity of magmatic fluid. Mixing is also the impetus of leaching copper from potassic to the phyllic zone. It is possible to conclude that all these procedures are controlled by the main faults of district having NW–SE trend. Two fundamental events affecting the mineralization are cooling ore-bearing fluids and magnetite (±pyrite) emplacement. The latter one is formed in potassic and phyllic alteration zone in which copper-bearing fluids have interaction with magnetite minerals and so chalcopyrite minerals have been formed nearby magnetites. Temperature and pressure of hydrothermal fluid differentiation could be applied as a predictive tool to discriminate between barren and productive copper porphyry deposits. A simple comparison of temperature and pressure variations between Daraloo deposit and other copper porphyry deposits located in the same belt of Iran (Sahand-Bazman belt) illuminates that Daraloo system has high range of pressure implying deeper exsolution of hydrothermal fluid. On the other hand, economic mineralization has direct relationship with temperature range of orthomagmatic fluids so that if a deposit has a wide range of high temperature fluids, it could be inferred as a barren deposit. In conclusion, it could be inferred that Daraloo district can be categorized as a sub-economic porphyry deposit. On the other hand, restricted formation of chalcopyrite and the other copper-bearing minerals besides large amounts of magnetite and pyrite can approve obviously the low grade of mineralization in Daraloo district. 相似文献
5.
The Miduk porphyry copper deposit is located in Kerman province, 85 km northwest of the Sar Cheshmeh porphyry copper deposit, Iran. The deposit is hosted by Eocene volcanic rocks of andesitic–basaltic composition. The porphyry‐type mineralization is associated with two Miocene calc‐alkaline intrusive phases (P1 and P2, respectively). Five hypogene alteration zones are distinguished at the Miduk deposit, including magnetite‐rich potassic, potassic, potassic–phyllic, phyllic and propylitic. Mineralization occurs as stockwork, dissemination and nine generations (magnetite, quartz–magnetite, barren quartz, quartz‐magnetite‐chalcopyrite‐anhydrite, chalcopyrite–anhydrite, quartz‐chalcopyrite‐anhydrite‐pyrite, quartz‐molybdenite‐anhydrite ± chalcopyrite ± magnetite, pyrite, and quartz‐pyrite‐anhydrite ± sericite) of veinlets and veins. Early stages of mineralization consist of magnetite rich veins in the deepest part of the deposit and the main stage of mineralization contains chalcopyrite, magnetite and anhydrite in the potassic zone. The high intensity of mineralization is associated with P2 porphyry (Miduk porphyry). Based on petrography, mineralogy, alteration halos and geochemistry, the Miduk porphyry copper deposit is similar to those of continental arc setting porphyry copper deposits. The Re‐Os molybdenite dates provide the timing of sulfide mineralization at 12.23 ± 0.07 Ma, coincident with U/Pb zircon ages of the P2 porphyry. This evidence indicates a direct genetic relationship between the Miduk porphyry stock and molybdenite mineralization. The Re‐Os age of the Miduk deposit marks the main stage of magmatism and porphyry copper formation in the Central Iranian volcano‐plutonic belt. 相似文献
6.
The Kahang porphyry Cu deposit, located northeast of Isfahan city in central of Iran, is associated with a composite Miocene stock and ranges in composition from diorite through granodiorite to quartz-monzonite. Field observations and petrographic studies show that the emplacement of the Kahang stock occurred in several pulses, each associated with its related hydrothermal activity. Early hydrothermal alteration started with a potassic style in the central part of the system and produced a secondary biotite–K-feldspar–magnetite assemblage accompanied by chalcopyrite and pyrite mineralization. Propylitic alteration that took place at the same time as the potassic alteration occurred in the peripheral portions of the stock. Subsequent phyllic alteration overprinted earlier potassic and propylitic alterations. Biotite grains from the potassic and phyllic zones show distinct chemical compositions. The FeO, TiO2, MnO, K2O, and Na2O concentrations in biotite from the phyllic alteration zone are lower than those from the potassic alteration zone. The F and Cl contents of biotite from the potassic alteration zone display relatively high positive correlation with the XMg. The fluorine intercept values [IV(F)] from the potassic and phyllic alteration zones are strongly correlated with the fluorine/chlorine intercept values [IV(F/Cl)]. Biotite geothermometry for the potassic and phyllic alteration zones, based on the biotite geothermometer of Beane (1974), yields a temperature range of 422° to 437 °C (mean = 430 °C) and 329° to 336 °C (mean = 333 °C), respectively. The position of data in log (XF/XOH) ratio vs. XMg and XFe diagram suggests that biotite formed under dissimilar composition and temperature conditions in the potassic and phyllic alteration zones. Calculated log fugacity ratios of (fH2O/fHF), (fH2O/fHCl), and (fHF/fHCl) show that hydrothermal fluids associated with the potassic alteration were distinctively different from those fluids associated with the phyllic alteration zone at Kahang porphyry Cu deposit. The results of this research indicate that the chemistry of biotite is related to the chemical composition of the magma and the prevailing physical conditions during crystallization. 相似文献
7.
The Shapinggou porphyry Mo deposit, one of the largest Mo deposits in Asia, is located in the Dabie Orogen, Central China. Hydrothermal alteration and mineralization at Shapinggou can be divided into four stages, i.e., stage 1 ore-barren quartz veins with intense silicification, followed by stage 2 quartz-molybdenite veins associated with potassic alteration, stage 3 quartz-polymetallic sulfide veins related to phyllic alteration, and stage 4 ore-barren quartz ± calcite ± pyrite veins with weak propylitization. Hydrothermal quartz mainly contains three types of fluid inclusions, namely, two-phase liquid-rich (type I), two- or three-phase gas-rich CO2-bearing (type II) and halite-bearing (type III) inclusions. The last two types of fluid inclusions are absent in stages 1 and 4. Type I inclusions in the silicic zone (stage 1) display homogenization temperatures of 340 to 550 °C, with salinities of 7.9–16.9 wt.% NaCl equivalent. Type II and coexisting type III inclusions in the potassic zone (stage 2), which hosts the main Mo orebodies, have homogenization temperatures of 240–440 °C and 240–450 °C, with salinities of 34.1–50.9 and 0.1–7.4 wt.% NaCl equivalent, respectively. Type II and coexisting type III inclusions in the phyllic zone (stage 3) display homogenization temperatures of 250–345 °C and 220–315 °C, with salinities of 0.2–6.5 and 32.9–39.3 wt.% NaCl equivalent, respectively. Type I inclusions in the propylitization zone (stage 4) display homogenization temperatures of 170 to 330 °C, with salinities lower than 6.5 wt.% NaCl equivalent. The abundant CO2-rich and coexisting halite-bearing fluid inclusion assemblages in the potassic and phyllic zones highlight the significance of intensive fluid boiling of a NaCl–CO2–H2O system in deep environments (up to 2.3 kbar) for giant porphyry Mo mineralization. Hydrogen and oxygen isotopic compositions indicate that ore-fluids were gradually evolved from magmatic to meteoric in origin. Sulfur and lead isotopes suggest that the ore-forming materials at Shapinggou are magmatic in origin. Re–Os dating of molybdenite gives a well-defined 187Re/187Os isochron with an age of 112.7 ± 1.8 Ma, suggesting a post-collisional setting. 相似文献
8.
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
9.
Rosia Poieni copper deposit,Apuseni Mountains,Romania: advanced argillic overprint of a porphyry system 总被引：2，自引：0，他引：2
The Rosia Poieni deposit is the largest porphyry copper deposit in the Apuseni Mountains, Romania. Hydrothermal alteration and mineralization are related to the Middle Miocene emplacement of a subvolcanic body, the Fundoaia microdiorite. Zonation of the alteration associated with the porphyry copper deposit is recognized from the deep and central part of the porphyritic intrusion towards shallower and outer portions. Four alteration types have been distinguished: potassic, phyllic, advanced argillic, and propylitic. Potassic alteration affects mainly the Fundoaia subvolcanic body. The andesitic host rocks are altered only in the immediate contact zone with the Fundoaia intrusion. Mg-biotite and K-feldspar are the main alteration minerals of the potassic assemblage, accompanied by ubiquitous quartz; chlorite, and anhydrite are also present. Magnetite, pyrite, chalcopyrite and minor bornite, are associated with this alteration. Phyllic alteration has overprinted the margin of the potassic zone, and formed peripheral to it. It is characterized by the replacement of almost all early minerals by abundant quartz, phengite, illite, variable amounts of illite-smectite mixed-layer minerals, minor smectite, and kaolinite. Pyrite is abundant and represents the main sulfide in this alteration zone. Advanced argillic alteration affects the upper part of the volcanic structure. The mineral assemblage comprises alunite, kaolinite, dickite, pyrophyllite, diaspore, aluminium-phosphate-sulphate minerals (woodhouseite-svanbergite series), zunyite, minamyite, pyrite, and enargite (luzonite). Alunite forms well-developed crystals. Veins with enargite (luzonite) and pyrite in a gangue of quartz, pyrophyllite and diaspore, are present within and around the subvolcanic intrusion. This alteration type is partially controlled by fractures. A zonal distribution of alteration minerals is observed from the centre of fractures outwards with: (1) vuggy quartz; (2) quartz + alunite; (3) quartz + kaolinite ± alunite and, in the deeper part of the argillic zone, quartz + pyrophyllite + diaspore; (4) illite + illite-smectite mixed-layer minerals ± kaolinite ± alunite, and e) chlorite + albite + epidote. Propylitic alteration is present distal to all other alteration types and consists of chlorite, epidote, albite, and carbonates. Mineral parageneses, mineral stability fields, and alteration mineral geothermometers indicate that the different alteration assemblages are the result of changes in both fluid composition and temperature of the system. The alteration minerals reflect cooling of the hydrothermal system from >400 °C (biotite), to 300–200 °C (chlorite and illite in veinlets) and to lower temperatures of kaolinite, illite-smectite mixed layers, and smectite crystallization. Hydrothermal alteration started with an extensive potassic zone in the central part of the system that passed laterally to the propylitic zone. It was followed by phyllic overprint of the early-altered rocks. Nearly barren advanced argillic alteration subsequently superimposed the upper levels of the porphyry copper alteration zones. The close spatial association between porphyry mineralization and advanced argillic alteration suggests that they are genetically part of the same magmatic-hydrothermal system that includes a porphyry intrusion at depth and an epithermal environment of the advanced argillic type near the surface.Editorial handling: B. Lehmann 相似文献
10.
金厂金矿18号矿体围岩蚀变发育顺序从早到晚为:钾化、硅化、绿泥石化、绢云母化、碳酸盐化、高蛉土化,从内往外依次发育青磐岩化带、绢英岩化带和钾化带.矿化出现在泥化和绢英岩化叠加处,以及泥化和青磐岩化叠加处.通过短波红外光谱测试技术,识别出本矿区有26种蚀交矿物,其中白云母含量与金矿体呈正相关,说明绢云母化与金矿化关系密切;青磐岩化带蚀变矿物组合为绿泥石+绿帘石+伊利石±埃洛石±蒙脱石±石英;钾化带蚀变矿物组合为钾长石+高岭石+埃洛石±蒙脱石±石英;绢英岩化带蚀变矿物组合为绢云母+埃洛石±蒙脱石±高岭石±石英. 相似文献
11.
12.
Porphyry Cu-Mo-Au mineralisation with associated potassic and phyllic alteration, an advanced argillic alteration cap and epithermal quartz-sulphide-gold-anhydrite veins, are telescoped within a vertical interval of 400-800 m on the northeastern margin of the Thames district, New Zealand. The geological setting is Jurassic greywacke basement overlain by Late Miocene andesitic-dacitic rocks that are extensively altered to propylitic and argillic assemblages. The porphyry Cu-Mo-Au mineralisation is hosted in a dacite porphyry stock and surrounding intrusion breccia. Relicts of a core zone of potassic K-feldspar-magnetite-biotite alteration are overprinted by phyllic quartz-sericite-pyrite or intermediate argillic chlorite-sericite alteration assemblages. Some copper occurs in quartz-magnetite-chlorite-pyrite-chalcopyrite veinlets in the core zone, but the bulk of the copper and the molybdenum are associated with the phyllic alteration as disseminated chalcopyrite and as molybdenite-sericite-carbonate veinlets. The advanced argillic cap has a quartz-alunite-dickite core, which is enveloped by an extensive pyrophyllite-diaspore-dickite-kaolinite assemblage that overlaps with the upper part of the phyllic alteration zone. Later quartz-sphalerite-galena-pyrite-chalcopyrite-gold-anhydrite-carbonate veins occur within and around the margins of the porphyry intrusion, and are associated with widespread illite-carbonate (argillic) alteration. Multiphase fluid inclusions in quartz stockwork veins associated with the potassic alteration trapped a highly saline (50-84 wt% NaCl equiv.) magmatic fluid at high temperatures (450 to >600 °C). These hypersaline brines were probably trapped at a pressure of about 300 bar, corresponding to a depth of 1.2 km under lithostatic conditions. This shallow depth is consistent with textures of the host dacite porphyry and reconstruction of the volcanic stratigraphy. Liquid-rich fluid inclusions in the quartz stockwork veins and quartz phenocrysts trapped a lower salinity (3-20 wt% NaCl equiv.), moderate temperature (300-400 °C) fluid that may have caused the phyllic alteration. Fluid inclusions in the quartz-sphalerite-galena-pyrite-chalcopyrite-gold-anhydrite-carbonate veins trapped dilute (1-3 wt% NaCl equiv.) fluids at 250 to 320 °C, at a minimum depth of 1.0 km under hydrostatic conditions. Oxygen isotopic compositions of the fluids that deposited the quartz stockwork veins fall within the 6 to 10 range of magmatic waters, whereas the quartz-sulphide-gold-anhydrite veins have lower '18Owater values (-0.6 to 0.5), reflecting a local meteoric water (-6) influence. A '18O versus 'D plot shows a trend from magmatic water in the quartz stockwork veins to a near meteoric water composition in kaolinite from the advanced argillic alteration. Data points for pyrophyllite and the quartz-sulphide-gold-anhydrite veins lie about midway between the magmatic and meteoric water end-member compositions. The spatial association between porphyry Cu-Mo-Au mineralisation, advanced argillic alteration and quartz-sulphide-gold-anhydrite veins suggests that they are all genetically part of the same hydrothermal system. This is consistent with K-Ar dates of 11.6-10.7 Ma for the intrusive porphyry, for alunite in the advanced argillic alteration, and for sericite selvages from quartz-gold veins in the Thames district. 相似文献
13.
雪鸡坪铜矿床产于印支晚期石英二长闪长玢岩-石英闪长玢岩-石英二长斑岩复式侵入体内,为一斑岩型铜矿床。矿床形成经历了多阶段热液成矿作用,主要有微细脉浸染状黄铁矿±黄铜矿-石英、细脉状辉钼矿±黄铁矿±黄铜矿-石英及微细脉状贫硫化物-石英-方解石等。流体包裹体岩相学、显微测温、激光拉曼及碳、氢、氧同位素综合研究表明,微细脉浸染状黄铁矿±黄铜矿-石英阶段石英中主要发育含Na Cl子矿物三相及气液两相包裹体,与含矿的石英二长斑岩石英中发育的流体包裹体特征相似,表明成矿流体主要为中高温、高盐度Na Cl-H2O体系热液,可能主要来源于印支期石英二长斑岩侵入体;辉钼矿±黄铁矿±黄铜矿-石英中主要发育含CO2三相及气液两相包裹体,成矿流体为中温、低盐度Na Cl-CO2-H2O体系热液,与前者来源明显不同;贫硫化物-石英-方解石石英中主要发育气液两相包裹体,成矿流体为中低温、低盐度Na Cl-H2O体系热液,推测其可能较多来自于大气降水。因此,雪鸡坪铜矿床为不同来源、不同地球化学性质热液叠加成矿作用的结果。 相似文献
14.
巴达铜金矿位于藏东富碱斑岩带南段,是藏东地区近年来新发现的大型铜金矿。虽然对巴达铜金矿开展了大量勘查工作,但对该矿床的成因尚未取得共识。本文基于详细的野外调研、岩心与坑道编录及系统的镜下鉴定,对巴达铜金矿床地质特征进行研究。巴达矿床主要产于石英二长斑岩中,局部产于斑岩和砂岩地层的接触带内。矿床发育的围岩蚀变主要为青磐岩化、钾化、绢英岩化,高岭土化、蛋白石化、蒙脱石化次之,蚀变分带从内向外依次为钾硅酸盐化带、绢英岩化带、青磐岩化带、高岭土化带,铜金矿体主要赋存于钾硅酸盐化和绢英岩化带内,铜矿化主要以黄铜矿形式产出,金矿化主要以银金矿形式产于白云石±石英+细粒黄铁矿±黄铜矿脉中,铜矿化与金矿化呈正相关,矿体的产出受北西向逆冲断层的控制。与典型斑岩和浅成低温热液矿床不同,巴达铜金矿化主要产于白云石±石英+黄铁矿脉中;矿床内既发育碳酸盐、伊利石、绢云母和黄铁矿、黄铜矿、方铅矿、黝铜矿、低FeS闪锌矿等一套中硫型浅成低温热液矿床的蚀变矿物组合,又发育符合碱性斑岩系统的特征矿物赤铁矿。基于以上特征判断,巴达铜金矿矿床成因类型应为与富碱斑岩有关的浅成低温热液矿床,巴达铜金矿矿床成因的厘定,为下一步找矿提供了理论指导。 相似文献
15.
The San Jorge porphyry copper deposit (SJPCD) is hosted by Carboniferous clastic sedimentary rocks and Permian intrusions located within the Permo-Triassic belt of Chile and Argentina. Its hypogene mineralization and alteration are products of superposed orthomagmatic and hydrothermal events that were strongly fault controlled. Copper related to orthomagmatic processes includes disseminated chalcopyrite in the matrix of porphyritic granodiorite and andesite, and chalcopyrite with tourmaline and quartz in breccias, both of which have accompanying potassic alteration. Soon thereafter, disseminated chalcopyrite is associated with a structurally controlled silicification of the sedimentary sequence. Finally, multiple episodes of hydrofracturing, probably driven by a deep-seated intrusion, deposited sulfide minerals in veinlets throughout the sedimentary sequence; the centers of these systems are characterized by potassic alteration. Total sulfides, which include chalcopyrite, pyrite, arsenopyrite, and pyrrhotite, and pyrite:chalcopyrite form a linear NNE trend, parallel to the main faults. Quartz–sericite is the dominant alteration and is ubiquitous. Zones of potassic alteration can be delineated even though phyllic alteration can be superposed. Much of the system evolved under reducing conditions. Despite uplift along a reverse fault during the Tertiary, and subsequent erosion, the system is preserved at high levels. Supergene processes redistributed copper in secondary oxides and sulfides. These processes were more effective where the deposit is covered by unconsolidated alluvial sediments. The unique history of the San Jorge deposit renders it an important variation of porphyry copper-style mineralization. 相似文献
16.
Marta Franchini Agnes Impiccini David Lentz Francisco Javier Ríos Sol O'Leary Josefina Pons Abel Isidoro Schalamuk 《Ore Geology Reviews》2011,41(1):49-74
Agua Rica (27°26′S–66°16′O) is a world class Cu–Au–Mo deposit located in Catamarca, Argentina. In the E–W 6969400 section examined, the Seca Norte and the Trampeadero porphyries that have intruded the metasedimentary rock are cut by interfingered igneous and hydrothermal heterolithic and monolithic breccias, and sandy dikes. Relic biotite and K-feldspar of the early potassic alteration (370° to > 550 °C) with Cu (Mo–Au) mineralization are locally preserved and encapsulated in a widespread, white mica + quartz + rutile or anatase halo (phyllic alteration) with pyrite + covellite that suggests fluids with temperatures ≤ 360 °C and high f(S2). The Trampeadero porphyry and the surrounding metasedimentary rock with phyllic alteration have molybdenite in stringers and B-type quartz veinlets and the highest Mo grades (> 1000 ppm).Multistage advanced argillic alteration overprinted the earlier stages. Early andalusite ± pyrite ± quartz is preserved in the roots of the argillic halo rimmed by an alumina–silica material and white micas. This alteration assemblage is considered to have been formed at temperatures ≥ 375 °C from condensed magmatic vapor. At higher levels, pyrophyllite replaces muscovite and illite in clasts of hydrothermal breccias in the center and east sector of the study section, suggesting temperatures of 280 to 360 °C. Clasts of vuggy silica in the uppermost levels of the central breccia, indicates that at lower temperatures (< 250 °C), fluids reached very low pH (pH < 2). In this early stage of the advanced argillic alteration, hydrothermal fluids seem to have not precipitated sulfides or sulfosalts.Hydrothermal brecciation was concurrent with fluid exsolution (↑? V), which precipitated intermediate-temperature advanced argillic alunite (svanbergite + woodhouseite) ± diaspore ± zunyite as breccia cement along with abundant covellite + pyrite + enargite ± native sulfur ± kuramite at intermediate depths and in lateral transitional zones to unbrecciated rocks. This mineral assemblage indicates temperatures near 300 °C, oxidized and silica-undersaturated hydrothermal fluids with high sulfur fugacity to prevent gold precipitation. Multiple generations of pyrite, emplectite, colusite, Pb- and Bi-bearing sulfosalts, and native sulfur with Au and Ag, accompanied by alunite introduction in the upper level breccias, probably occurred at lower temperatures, but still high sulfur and oxygen activity. An independent Zn and Pb (as galena) mineralization stage locally coincides with Au–Ag and sulfosalts, and advanced at depth, controlled by fractures and overprinting much of the previous mineralization. A later paragenesis of veinlets of alunite + woodhouseite + svanvergite + pyrite ± enargite that cut the phyllic halo suggests temperatures ~ 250 °C and without woodhouseite + svanvergite, temperatures ~ 200 °C. Kaolinite occurs in the phyllic halo as a late mineral in clots and in veinlets thus, in this zone, the fluid had cooled enough for its formation. 相似文献
17.
Lead isotope compositions of nine sulfide concentrates from ore samples from the Sar-Cheshmeh deposit are reported. They range from virtually unaltered granodiorite through varying degrees of potassic alteration to ores showing strong phyllic alteration (sericite veins). The samples without strong phyllic alteration have fairly uniform lead isotope compositions around 206Pb/204Pb=18.6, 207Pb/204Pb=15.6, and 208Pb/204Pb=38.7. Two samples with sericite veins have markedly more radiogenic lead. It is concluded that the fluid responsible for the potassic alteration and the associated mineralization was essentially magmatic, whereas convecting meteoric water from the country rock acted as a mineralizing solution during phyllic alteration. In the context of the plumbotectonics model, the deposit has a typical orogen signature intermediate between primitive and mature island-arc settings. 相似文献
18.
The Siah-Kamar porphyry Mo deposit, located in the western Alborz-Azarbayjan magmatic belt, is the first and largest Mo deposit in the Iran. This deposit is mainly hosted by an I-type, shoshonitic quartz monzonite to monzonite intrusion and also extends in the surrounding lower to middle Eocene volcanic rocks. The geochemical features of the Siah-Kamar intrusion show enrichment in large-ion lithophile elements (LILE) and light rare earth elements (LREE), and significant negative anomalies of Nb, Ta and Ti analogues to the magmas derived from metasomatized sub-continental mantle. Porphyry molybdenum mineralization is associated with potassic, sericitic, argillic, and propylitic alteration zones. Mineralization occurs in disseminated form, in veins/veinlets and in hydrothermal breccias. The main ore minerals comprise molybdenite, chalcopyrite and bornite. The Microthermometric analyses at Siah-Kamar deposit showed that the halite-bearing inclusions contain high salinity (30.9–60.7 wt% NaCl eq.) with homogenization temperature ranging from 226 °C to 397 °C. The homogenization temperature of two phase liquid-rich inclusions range between 224 °C and 375 °C. The salinity of this type inclusions range from 0.6 to 7.5 wt% NaCl equivalent. The two-phase vapor-rich fluid inclusions homogenized at 270 °C to 397 °C. The salinity of this type fluid inclusions lie within the range of 0.6 to 4.24 wt% NaCl equivalent. Coexisting two phase V-rich and L-rich fluid inclusions in quartz associated with molybdenite provide evidence for boiling at 270 °C to 400 °C. The δ18Owater values of quartz in the molybdenite-bearing veins vary from +2.16 to +4.05‰, suggesting a magmatic origin for the ore-forming fluids. Re-Os isotopic dating of molybdenite indicated a mineralization age of 41.9 ± 3.6 Ma. The Re concentration in molybdenite suggests incorporation of mantle derived melt with crustal materials. The late Eocene magmatism along the western Alborz-Azarbayjan magmatic zone resulted from the Neo-Tethys subduction beneath the Iranian plateau. The Siah-Kamar monzonitic intrusion hosting the Mo deposit, could be considered as an example among the late Eocene intrusions within the western Alborz-Azarbayjan magmatic zone for any further exploration in this zone. 相似文献
19.
El Galeno and Michiquillay are early to middle Miocene Cu–Au–Mo porphyry-related deposits located in the auriferous Cajamarca
district of northern Peru. The El Galeno deposit (486 Mt at 0.57% Cu, 0.14 g/t Au and 150 ppm Mo) is associated with multiple
dioritic intrusions hosted within Lower Cretaceous quartzites and shales. Emplacement of the porphyry stocks (17.5–16.5 Ma)
in a hanging wall anticline was structurally controlled by oblique faults superimposed on early WNW-trending fold-thrust structures.
Early K-feldspar–biotite–magnetite (potassic) alteration was associated with pyrite and chalcopyrite mineralisation. A quartz–magnetite
assemblage that occurs at depth has completely replaced potassically altered rocks. Late- and post-mineralisation stocks are
spatially and temporally related to weak quartz–muscovite (phyllic) alteration. High Au grades are associated with early intrusive
phases located near the centre of the deposit. Highest Cu grades (~0.9% Cu) are mostly associated with a supergene enrichment
blanket, whilst high Mo grades are restricted to contacts with the metasedimentary rocks. The Michiquillay Cu–Au–Mo deposit
(631 Mt at 0.69% Cu, 0.15 g/t Au, 100–200 ppm Mo) is associated with a Miocene (20.0–19.8 Ma) dioritic complex that was emplaced
within the hanging wall of a back thrust fault. The intrusive complex is hosted in quartzites and limestones. The NE-trending
deposit is crosscut by NNW-trending prospect-scale faults that influenced both alteration and metal distribution. In the SW
and NE of the deposit, potassic alteration zones contain moderate hypogene grades (0.14 g/t Au and 0.8% Cu) and are characterised
by chalcopyrite and pyrite mineralisation. The core of the deposit is defined by a lower grade (0.08 g/t Au and 0.57% Cu)
phyllic alteration that overprinted early potassic alteration. Michiquillay contains a supergene enrichment blanket of 45–80 m
thickness with an average Cu grade of 1.15%, which is overlain by a deep leached cap (up to 150 m). Cu–Au–Mo (El Galeno-Michiquillay)
and Au-rich (Minas Conga) deposits in the Cajamarca region are of similar age (early–middle Miocene) and intrusive rock type
(dioritic) associations. Despite these geochronological and geochemical similarities, findings from this study suggest variation
in metal grade between the hybrid-type and Au-rich deposits result from a combination of physio-chemical factors. These include
variations in temperature and oxygen fugacity conditions during hypogene mineralisation resulting in varied sulphide assemblages,
host rock type, precipitation of ubiquitous hydrothermal magnetite, and late hydrothermal fluid flow resulting in a well-developed
phyllic alteration zone. 相似文献
20.
Guangming LI Jinxiang LI Kezhang QIN Ji DUO Tianping ZHANG Bo XIAO Junxing ZHAO 《Resource Geology》2012,62(1):99-118
The Duobuza gold‐rich porphyry copper district is located in the Bangongco metallogenetic belt in the Bangongco‐Nujiang suture zone south of the Qiangtang terrane. Two main gold‐rich porphyry copper deposits (Duobuza and Bolong) and an occurrence (135 Line) were discovered in the district. The porphyry‐type mineralization is associated with three Early Cretaceous ore‐bearing granodiorite porphyries at Duobuza, 135 Line and Bolong, and is hosted by volcanic and sedimentary rocks of the Middle Jurassic Yanshiping Formation and intermediate‐acidic volcanic rocks of the Early Cretaceous Meiriqie Group. Simultaneous emplacement and isometric distribution of three ore‐forming porphyries is explained as multi‐centered mineralization generated from the same magma chamber. Intense hydrothermal alteration occurs in the porphyries and at the contact zone with wall rocks. Four main hypogene alteration zones are distinguished at Duobuza. Early‐stage alteration is dominated by potassic alteration with extensive secondary biotite, K‐feldspar and magnetite. The alteration zone includes dense magnetite and quartz‐magnetite veinlets, in which Cu‐Fe‐bearing sulfides are present. Propylitic alteration occurs in the host basic volcanic rocks. Extensive chloritization‐silicification with quartz‐chalcopyrite or quartz‐molybdenite veinlets superimposes on the potassic alteration. Final‐stage argillic alteration overlaps on all the earlier alteration. This alteration stage is characterized by destruction of feldspar to form illite, dickite and kaolinite, with accompanying veinlets of quartz + chalcopyrite + pyrite and quartz + pyrite assemblages. Cu coexists with Au, which indicates their simultaneous precipitation. Mass balance calculations show that ore‐forming elements are strongly enriched during the above‐mentioned three alteration stages. 相似文献