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1.
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
2.
The Dexing deposit, located in the Circum-Pacific ore belt, is the largest porphyry copper deposit in eastern China. It is composed of 3 separate plutons, which host three mines: Tongchang, Fujiawu and Zhushahong mines. The porphyritic granodiorite samples studied in this investigation were collected from the Tongchang ore-forming pluton of this giant deposit. This paper presents electron microprobe analyses of biotite, apatite, amphibole, plagioclase, potassium feldspar and rehomogenized glassy melt inclusions from the Tongchang porphyritic granodiorites. Petrographic observations of the samples are consistent with portions of the granodioritic magma represented by our samples being overprinted by potassic hydrothermal fluid which variably altered these minerals.All of the studied micas are Mg-rich biotites. The biotites are separated into altered magmatic and secondary types based on their petrographic and geochemical characteristics. The phlogopite components of the secondary biotites are typically higher than those of the altered magmatic biotites, and the XMg values of all biotites correlate negatively with Cl contents, consistent with the Mg–Cl avoidance principle. The XMg values also correlate negatively with (K2O + Na2O + BaO), FeO and TiO2 for both generations of biotites. The calculated log (fH2O/fHCl) values (for 690 K) of the coexisting potassic fluids, which are determined from the altered magmatic biotite compositions, range from 4.43 to 4.67, and are very similar to those of other major porphyry deposits. However, the log(fH2O/fHF) and log(fHF/fHCl) values for the same batch of hydrothermal fluids are significant higher and lower than those of these other porphyry deposits, respectively.The Cl concentrations of amphiboles and melt inclusions range from 0.18 to 0.32 wt.% and 0.15 to 0.44 wt.%, respectively. Most apatites trapped in biotite and plagioclase phenocrysts display a bimodal Cl distribution: 0.19 to 1.35 wt.% and 1.48 to 3.73 wt.%. Similarly, the S contents of the apatite also show a distinct bimodal distribution reflecting the effects of variable anhydrite saturation during evolution of the Tongchang melt and variable dissolution of anhydrite by saline aqueous fluids. The Cl contents of the apatites from the Tongchang system are typically higher than those of other studied porphyry deposits. Furthermore, the Cl contents of the melt inclusions are at or very near the Cl saturation levels (0.36 to 0.46 wt.% at 850 °C and 50 MPa and 0.42 to 0.54 wt.% at 850 °C and 200 MPa) for these melt compositions at shallow crustal pressures. These findings suggest that the area of the granodioritic magma represented by our samples, and perhaps the bulk of the Tongchang granodioritic magma was rich in Cl. The melt inclusion compositions are consistent with a high-salinity, hydrosaline liquid being exsolved directly from the granodioritic melt directly. This high-salinity hydrosaline liquid was likely very efficient at dissolving, transporting and precipitating ore metals in the mineralizing magmatic–hydrothermal system. 相似文献
3.
The Sisson Brook W–Mo–Cu deposit was formed by hydrothermal fluids likely related to the Nashwaak Granites (muscovite–biotite granite, Group I; and biotite granite, Group II) and related dykes (biotite granitic dykes, Group III; and a feldspar–biotite–quartz porphyry dyke, Group IV). Chemical data obtained using EPMA and LA-ICP-MS data of primary magmatic biotites were used to investigate magmatic processes and associated hydrothermal fluids.Trace element features of biotite in the Group I two-mica granite suggest other magmatic processes along with a simple fractional crystallization. The K/Rb ratios and compatible elements (Cr, Ti, Co, V, and Ba) in biotite from Groups II, III, and IV decrease, whereas incompatible elements including Ta, Tl, Ga, Cs, Li, and Sn increase with magma fractionation. No correlation of Cu, W and Mo with K/Rb ratios is evident, suggesting that partitioning of Cu, W, and Mo into biotite may not be entirely controlled by magma fractionation.Halogen fugacity of the parental magma of the Nashwaak Granites and related dykes, calculated from zircon saturation temperature shows that Group I has high fHF/fCl ratios (broadly higher than 0), similar to the plutons at the Henderson porphyry Mo deposit. The fHF/fCl ratios of the other groups are generally lower than 0, comparable to the Santa Rita porphyry Cu deposit. The fH2O/fHCl and fH2O/fHF ratios inferred from biotite in the Nashwaak Granites and related dykes range from 3 to 5 and from 4 to 5, respectively. The inferred oxygen fugacity shows that the dyke phases (Groups III and IV) have the oxygen fugacity around the nickel–nickel oxide buffer. The plutonic phases (Groups I and II) have the oxygen fugacity around the quartz–fayalite–magnetite (QFM) buffer at high temperatures and oxidized to nickel–nickel oxide buffer at lower temperatures. This oxidation process in the plutonic phases (Groups I and II) could be caused by H2 release at or near H2O vapor saturation at high H2O/Fe2 +. The magma associated with the biotite dykes (Group III) is more likely the source of the hydrothermal fluids at the Sisson Brook deposit since it has the highest differentiation degree and seems to have formed in an oxidized setting, necessary for Mo to concentrate in the late stage fluids. 相似文献
4.
《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
5.
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
6.
Primary ore-forming minerals retain geochemical signatures of magmatic crystallization information and can reveal the petrochemical conditions prevalent at the time of their formation. The Baogutu deposit is a typical reduced porphyry Cu deposit. Amphibole and biotite Fe3+/ΣFe ratios, minerals (feldspar, biotite, amphibole, zircon and apatite), in situ elemental and apatite Nd isotopic compositions were determined by Mössbauer spectroscopy, electron probe microanalysis, and laser ablation multiple-collection inductively coupled plasma mass spectrometry, respectively, to investigate the magma oxidation state, petrogenesis, source features, and to constrain the carbon species at magmatic stages for the intrusive phases. The results show that the primary plagioclase and amphibole in the mineralized diorite to granodiorite porphyry and post ore hornblende diorite porphyry are distinct (An26-55 versus An60-69; Mg-hornblende versus tschermakite). In particular, the amphibole shows distinct major and trace element compositions with light rare earth element enrichments and negative Eu anomalies in Mg-hornblende and light rare earth element depletions and no Eu anomalies in tschermakite. All the analyzed biotites are primary igneous phases with a biotite phenocryst profile showing significant variations of Zn, Cr, Sc and Sr from core to rim. These results may indicate the occurrence of mixing between two distinct magmas during mineral formation. Titanium in zircon and Si1 in amphibole thermometries indicate that magma crystallized at >900 °C and continued to ∼650 °C. In situ apatite Nd isotope (εNd(t) = 5.6–7.6, TDM2 = 620–460 Ma), indicate absence of significant reduced sedimentary contamination and the source of juvenile lower crust. Slightly decreasing Fe3+/ΣFe ratios from biotite and amphibole to whole rock indicate decreasing oxygen fugacity during magma crystallization. Recalculated biotite compositions according to Fe3+/ΣFe ratios indicate fO2 values of less than Ni-NiO buffer (NNO) which show slightly lower values than that estimated according to zircon/melt distribution coefficients Ce anomalies (∼ΔNNO + 0.6). These values are consistent with the features of reduced porphyry Cu deposits. Crystallization of other mineral phases significantly affects the reliability of oxybarometer of zircon/melt distribution coefficients Eu anomalies and Mn contents in apatite. This oxidation state suggests that only CO2 was present at the magmatic stage, and implies that CH4 formed during CO2 reduction occurring later hydrothermal alteration. The alteration of primary amphibole to actinolite released Ti, Al, Fe, Mn, Na and K to the fluid with later precipitation of titanite, albite and minor ilmenite and magnetite during actinolite alteration. 相似文献
7.
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
8.
The Yandong porphyry copper deposit, located in the Eastern Tianshan Mountains, Xinjiang, China, is part of the Central Asian Orogenic Belt. The Yandong deposit is hosted by a volcanic complex in the Early Carboniferous Qi’eshan Group and a felsic intrusion. The complex consists of andesite, basalt, diorite porphyry, and porphyritic quartz diorite. The felsic intrusion is a plagiogranite porphyry emplaced within the complex. The diorite porphyry and plagiogranite porphyry yield SIMS zircon U–Pb ages of 340.0 ± 3 and 332.2 ± 2.3 Ma, respectively. Element geochemistry shows that both the complex and plagiogranite porphyry formed in the Dananhu–Tousuquan island arc, a Carboniferous magmatic arc.The diorite porphyry and plagiogranite porphyry are host porphyries, but the plagiogranite porphyry is a productive porphyry. It caused the porphyry-style Cu mineralization and associated alteration. The alteration assemblages include early potassic and propylitic assemblages. These were overprinted by a chlorite–sericite assemblage, which in turn was overprinted by a late phyllic assemblage. The phyllic alteration is associated with the highest Cu grades. The mineralization is recognized to include three stages, from early to late: stage 1, a potassic alteration associated with a chalcopyrite + pyrite assemblage; stage 2, represented by chlorite–sericite alteration with a chalcopyrite + pyrite assemblage; and stage 3, the main-ore stage that is marked by phyllic alteration with chalcopyrite + pyrite ± molybdenite and producing more than 70% of the total copper production at Yandong. Yandong may represent a common scenario for Paleozoic porphyry Cu systems in the Central Asian Orogenic Belt. 相似文献
9.
The recently discovered Longtougang skarn and hydrothermal vein Cu–Zn deposit is located in the North Wuyi area, southeastern China. The intrusions in the ore district comprise several small porphyritic biotite monzonite, porphyritic monzonite, and porphyritic granite plutons and dikes. The mineralization is zoned from a lower zone of Cu-rich veins and Cu–Zn skarns to an upper zone of banded Zn–Pb mineralization in massive epidote altered rocks. The deposit is associated with skarn, potassic, epidote, greisen, siliceous, and carbonate alteration. Molybdenite from the Cu-rich veins yielded a Re–Os isochron age of 153.6 ± 3.9 Ma, which is consistent with U–Pb zircon ages of 154.0 ± 1.3 Ma for porphyritic monzonite, 154.0 ± 0.8 Ma for porphyritic biotite monzonite, and 152.0 ± 0.8 Ma for porphyritic granite. Geological observations suggest that the Cu mineralization is genetically related to the porphyritic biotite monzonite and porphyritic monzonite. All the zircons from intrusive rocks in the ore district are characterized by εHf(t) values between − 13.41 and − 4.38 and Hf model ages (TDM2) between 2054 and 1482 Ma, reflecting magmas derived mainly from a Proterozoic crustal source. Molybdenite grains from the deposit have Re values of 14.6–27.7 ppm, indicative of a mixed mantle–crust source. The porphyry–skarn abundant Cu and hydrothermal vein type Pb–Zn–Ag deposits in the North Wuyi area are related to the Late Jurassic porphyritic granites and Early Cretaceous volcanism, respectively. The Late Jurassic mineralization-related granites were derived from the crustal anatexis with some mantle input, which was triggered by asthenospheric upwelling induced by slab tearing during oblique subduction of the paleo-Pacific plate beneath the South China block, and the Early Cretaceous mineralization-related granitoids mainly from crust material formed within a series of NNE-trending basins during margin-parallel movement of the plate. 相似文献
10.
The Dongping gold deposit hosted in syenites is one of the largest hydrothermal gold deposits in China and composed of ore veins in the upper parts and altered zones in the lower parts of the ore bodies. Pervasive potassic alteration and silicification overprint the wall rocks of the ore deposit. The alteration minerals include orthoclase, microcline, perthite, quartz, sericite, epidote, calcite, hematite and pyrite, with the quartz, pyrite and hematite assemblages closely associated with gold mineralization. The phases of hydrothermal alteration include: (i) potassic alteration, (ii) potassic alteration - silicification, (iii) silicification - epidotization - hematitization, (iv) silicification - sericitization - pyritization and (v) carbonation. Mass-balance calculations in potassic altered and silicified rocks reveal the gain of K2O, Na2O, SiO2, HFSEs and transition elements (TEs) and the loss of REEs. Most major elements were affected by intense mineral reactions, and the REE patterns of the ore are consistent with those of the syenites. Gold, silver and tellurium show positive correlation and close association with silicification. Fluid inclusion homogenization temperatures in quartz veins range from 154 °C to 382 °C (peak at 275 °C–325 °C), with salinities of 4–9 wt.% NaCl equiv. At temperatures of 325 °C the fluid is estimated to have pH = 3.70–5.86, log fO2 = − 32.4 to − 28.1, with Au and Te transported as Au (HS)2− and Te22 − complexes. The ore forming fluids evolved from high pH and fO2 at moderate temperatures into moderate-low pH, low fO2 and low temperature conditions. The fineness of the precipitated native gold and the contents of the oxide minerals (e.g., magnetite and hematite) decreased, followed by precipitation of Au- and Ag-bearing tellurides. The hydrothermal system was derived from an alkaline magma and the deposit is defined as an alkaline rock-hosted hydrothermal gold deposit. 相似文献
11.
The Luoboling Cu–Mo deposit in the Zijinshan Orefield, Fujian province, southeastern China, is a large porphyry deposit hosted by the Sifang granodiorite and the Luoboling granodiorite porphyry. The largest Cu–Mo orebody is saddle-shaped with various types of hydrothermal veinlets. Intensive hydrothermal alteration in the deposit is characterized by outward zoning from potassic, overprinted by phyllic alteration, to phyllic and alunite–dickite alteration. Based on the mineral assemblages and crosscutting relationships of veins, the ore-forming process can be divided into three stages, namely: an early-stage K-feldspar + quartz ± magnetite ± molybdenite veins associated with potassic alteration; a middle-stage quartz + molybdenite + chalcopyrite + pyrite veins in phyllic zone; and a late-stage quartz ± gypsum veins in the phyllic and alunite–dickite alteration zones. Six molybdenite separates yield a Re−Os isochron age 104.6 ± 1.0 Ma, which is identical to the age of emplacement of the Sifang and Luoboling granodiorite porphyries. Three types of fluid inclusions (FIs) were observed at the Luoboling deposit: 1) NaCl–H2O (aqueous), 2) daughter mineral-bearing and 3) CO2–H2O fluid inclusions. FIs of the early and middle stages are predominantly vapor-rich aqueous and daughter mineral-bearing inclusions, together with minor CO2-rich and liquid-rich aqueous inclusions; whereas the late-stage minerals only contain liquid-rich aqueous inclusions. Homogenization temperatures and salinities of FIs trapped in the early-stage minerals range from 420 to 540 °C and 0.4 to 62.9 wt.% NaCl equiv., respectively. FIs of the middle-stage yield homogenization temperatures of 340 to 480 °C and salinities of 0.5 to 56.0 wt.% NaCl equiv. CO2 content and the oxygen fugacity (indicated by daughter minerals) of FIs trapped in middle-stage minerals are lower than those in the early stage. The liquid-rich aqueous inclusions of the late-stage homogenize at temperatures of 140 to 280 °C, yielding salinities of 0.4 to 8.4 wt.% NaCl equiv. The minimum estimated pressures of the three stages are 30–70 MPa, 10–40 MPa and 1–10 MPa, respectively, corresponding to minimum ore-forming depths of 1–2.8 km. Fluids trapped in early, middle and late stages yield δD values of − 67‰ to − 54‰, − 54‰ to − 70‰, and − 62‰, and δ18O values of 5.4‰ to 6.7‰, 2.8‰ to 4.2‰, and − 2.1‰, respectively. Fluid boiling, which resulted in the formation of stockworks and the precipitation of sulfides, occurred in the early and middle stages. The fluids subsequently evolved into a low temperature, low salinity system in the late stage, along with an input of meteoric water. The Luoboling porphyry Cu–Mo system was developed in a transition from continental arc to back-arc extension region, which was related to the westward subduction of the paleo-Pacific plate beneath the Huanan Orogen. 相似文献
12.
The Jiama deposit, located in the eastern part of the well-known Gangdese Metallogenic Belt on the Tibetan Plateau, is the largest porphyry Cu–polymetallic system in the region, with the largest exploration budget, and is economically viable in the Gangdese Belt to undergo large-scale development. The deposit is well preserved and has experienced little erosion. The proven resources of the deposit are 7.4 Mt Cu, 0.6 Mt Mo, 1.8 Mt Pb + Zn, 6.65 Moz Au, and 360.32 Moz Ag. The results presented in this paper are based on geological and tectonic mapping, geological logging, and other exploration work performed by members of the Jiama Exploration Project Team over a period of 6 years. We propose that the Jiama porphyry Cu–polymetallic system is composed of skarn Cu–polymetallic, hornfels Cu–Mo, porphyry Mo ± Cu, and distal Au mineralization. The development of skarn Cu–polymetallic orebodies at the Jiama deposit was controlled mainly by the contact zone between porphyries and marbles, an interlayer detachment zone, and the front zone of a gliding nappe structure. The hornfels Cu–Mo and porphyry Mo ± Cu orebodies were controlled mainly by a fracture system related to intrusions, and the distal Au mineralization resulted from late-stage hydrothermal alteration.On the basis of field geological logging, optical microscopy, and chemical analysis, we verify that the alteration zones in the Jiama deposit include potassic, phyllic, propylitic, and argillic alteration, with a local lithocap, as well as endoskarn and exoskarn zones. The endoskarn occurs mainly as epidote alteration in quartz diorite porphyry and granite porphyry, and is cut by massive andradite veins. The exoskarn includes garnet–pyroxene and wollastonite skarn, in which the mineralogy and mineral chemical compositions display an outward zonation with respect to the source porphyry. From the proximal skarn to the intermediate skarn to the distal skarn, the garnet/pyroxene ratio varies from > 20:1 to ~ 10:1 to ~ 5:1, the garnet color varies from red-brown to brown-green to green-yellow, and the average composition of garnet varies from Ad80.1Gr18.9(Sp + Py)1.0 to Ad76.3Gr23(Sp + Py)0.7 to Ad59.5Gr39.5(Sp + Py)1.0, respectively. The pyroxene is not as variable in composition as the garnet, and is primarily light green to white diopside with a maximum hedenbergite content of ~ 20% and an average composition of Di88.6Hd8.9Jo2.5. From the proximal skarn to the intermediate skarn to the distal skarn, the mineralization changes from Cu–Mo to Cu ± Mo to Pb–Zn ± Cu ± Au ores, respectively. The wollastonite skarn displays no zonation and hosts mainly bornite mineralization. The Cu and Mo mineralization is closely related to the potassic and phyllic zones in the porphyry–hornfels.Zircons from four mineralized porphyries yield U–Pb ages of 15.96 ± 0.5 Ma, 15.72 ± 0.14 Ma, 15.59 ± 0.09 Ma, and 15.48 ± 0.08 Ma. The Re–Os ages of molybdenite from the skarn, hornfels, and porphyry are 15.37 ± 0.15 Ma, 14.67 ± 0.37 Ma, and 14.66 ± 0.27 Ma, respectively. The present results are consistent with the findings of previous research on fluid inclusions, isotopes, and other such aspects. On the basis of the combined evidence, we propose a porphyry Cu–polymetallic system model for the Jiama deposit and suggest a regional exploration strategy that can be applied to prospecting for porphyry-skarn mineralization in the Lhasa area. 相似文献
13.
The Yuchiling Mo deposit, East Qinling, China, belongs to a typical porphyry Mo system associated with high-K calc-alkaline intrusions. The pure CO2 (PC), CO2-bearing (C), aqueous H2O-NaCl (W), and daughter mineral-bearing (S) fluid inclusions were observed in the hydrothermal quartz. Based on field investigations, petrographic, microthermometric and LA-ICP-MS studies of fluid inclusions, we develop a five-stage fluid evolution model to understand the ore-forming processes of the Yuchiling deposit. The earliest barren quartz ± potassic feldspar veins, developed in intensively potassic alteration, were crystallized from carbonic-dominant fluids at high temperature (> 416 °C) and high pressure (> 133 MPa). Following the barren quartz ± potassic feldspar veins are quartz-pyrite veins occasionally containing minor K-feldspar and molybdenite, which were formed by immiscible fluids at pressures of 47–159 MPa and temperatures of 360–400 °C. The fluids were characterized by high CO2 contents (approximately 8 mol%) and variable salinities, as well as the highest Mo contents that resulted in the development of quartz-molybdenite veins. The quartz-molybdenite veins, accounting for > 90% Mo in the orebody, were also formed by immiscible fluids with lower salinity and lower CO2 content of 7 mol%, at temperatures of 340–380 °C and pressures of 39–137 MPa, as constrained by fluid inclusion assemblages. After the main Mo-mineralization, the uneconomic Cu-Pb-Zn mineralization occurred, as represented by quartz-polymetallic sulfides veins consisting of pyrite, molybdenite, chalcopyrite, digenite, galena, sphalerite and quartz. The quartz-polymetallic sulfide veins were formed by fluids containing 5 mol% CO2, with minimum pressures of 32–110 MPa and temperatures of 260–300 °C. Finally, the fluids became dilute (5 wt.% NaCl equiv) and CO2-poor, which caused the formation of late barren quartz ± carbonate ± fluorite veins at 140–180 °C and 18–82 MPa.It is clear that the fluids became more dilute, CO2-poor, and less fertile, with decreasing temperature and pressure from quartz-pyrite to late barren veins. Molybdenite and other sulfides can only be observed in the middle three stages, i.e., quartz-pyrite, quartz-molybdenite and quartz-polymetallic sulfide veins. These three kinds of veins are generally hosted in potassic altered rocks with remarkable K-feldspathization, but always partly overprinted by phyllic alteration. The traditional porphyry-style potassic–phyllic–propylitic alteration zoning is not conspicuous at Yuchiling, which may be related to, and characteristic of, the CO2-rich fluids derived from the magmas generated in intercontinental collision orogens.Among the fluid inclusions at Yuchiling, only the C-type contains maximum detectable Mo that gradationally decreases from 73 ppm in quartz-pyrite veins, through 19 ppm in quartz-molybdenite veins, and to 13 ppm in quartz-polymetallic sulfide veins, coinciding well with the decreasing CO2 contents from 8 mol%, through 7 mol%, to 5 mol%, respectively. Hence it is suggested that decreasing CO2 possibly results in decreasing Mo concentration in the fluids, as well as the precipitation of molybdenite from the fluids. This direct relationship might be a common characteristic for other porphyry Mo systems in the world.The Yuchiling Mo deposit represents a new type Mo mineralization, with features of collision-related setting, high-K calc-alkaline intrusion, CO2-rich fluid, and unique wall-rock alterations characterized by strong K-feldspathization and fluoritization. 相似文献
14.
The Trans-North China Orogen (TNCO), a Paleoproterozoic suture that amalgamates the Western and Eastern Blocks of the North China Craton (NCC), witnessed extensive magmatism and metallogeny during Mesozoic, associated with intraplate tectonics and differential destruction of the cratonic lithosphere. Here we investigate a suite of porphyry dykes surrounding the Mapeng batholith in the Fuping Complex within the TNCO in relation to the Mesozoic gold and molybdenum mineralization. The major element chemistry of these dykes show a range of SiO2 (57.92 to 69.47 wt.%), Na2O (3.20 to 4.77 wt.%), K2O (3.12 to 4.60 wt.%) and MgO (0.51 to 3.67 wt.%), together with high concentration of LREE and LILE, and relatively low contents of HREE and HFSE. The rocks display (La/Yb)N = 13.53–48.11, negative Nb, Ta, Th, U and Zr anomalies, and distinctly positive Ba, K and Sm anomalies. The mineralogy and geochemistry of the porphyry dykes indicate the rocks to be high-K calc-alkaline, and I-type, with adakitic features similar to those of the adjacent Mapeng batholith. The source magma for these rocks was derived from a mixture of reworked ancient continent crust and juvenile mantle materials. The zircon U–Pb data from these rocks show ages in the range of 124 to 129 Ma, broadly coinciding with the emplacement age of the Mapeng intrusion. The inherited zircons of ca. 2.5, 2.0 and 1.8 Ga in the dykes represent capture from the basement rocks during melting. The zircon Lu–Hf isotopic compositions show negative εHf(t) values varying from − 27.8 to − 11.3, with Hf depleted model ages (tDM) ranging from 1228 Ma to 1918 Ma and Hf crustal model ages (tDMC) of 1905 Ma to 2938 Ma, suggesting that the Mesozoic magmatism and associated metallogeny involved substantial recycling of ancient basement rocks of the NCC. We present an integrated model to evaluate the genesis of the porphyry systems and their relation to mineralization. We envisage that these dykes probably acted as stoppers (impermeable barriers) that prevented the leakage and run-off of the ore-bearing fluids, and played a key role in concentrating the gold and molybdenum mineralization. 相似文献
15.
《Lithos》2007,93(1-2):126-148
Fenite aureoles around carbonatite dykes, and alteration associated with Fe–REE–Nb ore bodies at Bayan Obo, Inner Mongolia, China, show alkali silicate assemblages containing aegirine–augite, (magnesio-)riebeckite, (magnesio-)arfvedsonite, and phlogopite, accompanied by varying amounts of apatite, albite and quartz. In both fenites and orebodies simple thermodynamic constraints indicate mineral parageneses are consistent with rock buffered cooling accompanied by the infiltration of a range of externally buffered hydrothermal fluids. Statistical analysis of amphibole chemistry indicates that even in apparently texturally well constrained paragenetic stages wide variations in chemistry occur in both the ore bodies and fenites. Much of this variation is attributable to the Mg and F content of amphibole, and is therefore interpreted as a result of variation in externally controlled variables (P, T, initial fluid composition) rather than internally controlled variables such as protolith composition. Similarities in chemistry exist between fenite and some ore body amphiboles. Thermodynamic analysis of the composition of biotite and apatite allows constraints to be placed on the F-content of hydrothermal fluids, and indicates relatively consistent compositions in fenites and orebodies (log aHF/aH2O = − 3.8 to − 3.6 at 300 °C and 1 kbar). Amphibole and biotite associated with niobate mineralization are both enriched in fluorine relative to the rest of the paragenesis, and biotite compositions indicate significantly higher HF activities in the hydrothermal fluid (log aHF/aH2O = − 2.6 at 300 °C and 1 kbar). The data presented here reinforce previous interpretations of the complex, multistage nature of mineralisation at Bayan Obo, but are still consistent with a direct involvement of carbonatite derived fluids during ore genesis. 相似文献
16.
Zhiguang Chen Lianchang Zhang Bo Wan Huaying Wu Nathan Cleven 《Ore Geology Reviews》2011,43(1):92-105
The Wunugetushan porphyry Cu–Mo deposit is located in the Manzhouli district of NE China, on the southern margin of the Mesozoic Mongol–Okhotsk Orogenic Belt. Concentric rings of hydrothermal alteration and Cu–Mo mineralization surround an Early–Middle Jurassic monzogranitic porphyry. The Cu–Mo mineralization is clearly related to the quartz–potassic and quartz–sericite alteration. Molybdenite Re–Os and groundmass 40Ar/39Ar of the host porphyry dates indicate that the ore-formation and porphyry-emplacement occurred at 177.6 ± 4.5 Ma and 179.0 ± 1.9 Ma, respectively. Geochemically, the host porphyry of the deposit is characterized by strong LREE/HREE fractionation, enrichment in LILE, Ba, Rb, U, Th and Pb, and depletion of HFSE, Nb, Ta, Ti and HREE. The Sr–Nd–Pb isotopic compositions of the porphyry display an varied initial (87Sr/86Sr)i ratio, a positive εNd(t) values and high 206Pb/204Pbt, 207Pb/204Pbt and 208Pb/204Pbt ratios. These data indicate that the magmatic source of the host porphyry comprised two end-members: lithospheric mantle metasomatized by fluids derived from the subducted slab; and continental crust. We infer that the primitive magma of the host porphyry was derived from crust–mantle transition zone. Based on regional geology and geochemistry of the host porphyry, the Wunugetushan deposit is suggested to form in a continental collision environment after closure of the Mongol–Okhotsk Ocean. 相似文献
17.
The Lermontovskoe deposit (∼48 Kt WO3; average 2.6% WO3, 0.24% Cu, 0.23 g/t Au) is situated in a W-Sn-Au metallogenic belt that formed in a collisional tectonic environment. This tungsten skarn deposit has a W-Au-As-Bi-Te-Sb signature that suggests an affinity with reduced intrusion-related Au deposits. The deposit is associated with an intrusion that is part of the ilmenite-series, high-K peraluminous granitoid (granodiorite to granite) suite. These rocks formed via mantle magma-induced melting of crustal sources.The deposit comprises reduced-type, pyroxene-dominated prograde and retrograde skarns followed by hydrosilicate (amphibole-chlorite-pyrrhotite-scheelite-quartz) and phyllic (muscovite/sericite-carbonate-albite-quartz-scheelite-sulfide, with abundant apatite) alteration assemblages. Fluid inclusions from the skarn assemblages indicate high-temperature (>500 °C), high-pressure (1400–1500 bars) and high-salinity (53–60 wt% NaCl-equiv.) magmatic-hydrothermal fluids. They were post-dated by high-carbonic, methane-dominate, low-salinity fluid at the hydrosilicate alteration stage. These fluids boiled at 360–380 °C and 1300–1400 bars. The subsequent phyllic alteration started again with a high-temperature (>450 °C), high-pressure (1000–1100 bars) and high-salinity (42–47 wt% NaCl-equiv.) fluid, with further incursion of high-carbonic, methane-dominated, low-salinity fluid that boiled at 390–420 °C and 1150–1200 bars. The latest phyllic alteration included the lower-temperature (340–360 °C), lower pressure (370–400 bars) high-carbonic, methane-dominated (but with higher CO2 fraction), low-salinity fluid, and then the low-temperature (250–300 °C) H2O-CO2-CH4-NaCl fluid, with both fluids boiled at the deposit level. The high-salinity aqueous fluids are interpreted to have come from crystallizing granitoid magma, whereas the reduced high-carbonic fluids probably came from a deeper mafic magma source. Both of these fluids potentially contributed to the W-Au-As-Bi-Te-Sb metal budget. Decreasing temperatures coupled with high aCa2+ and fluid boiling promoted scheelite deposition at all post-skarn hydrothermal stages.The deposit is characterized by limited downdip extent of mineralized zones and abundant coarse-grained muscovite-quartz (+apatite, scheelite) aggregates that formed at the phyllic alteration stage. Together with presence of high-temperature, high-pressure and high-salinity fluids directly exsolving from crystallizing magma, this suggests a root level of the mineralized magmatic-hydrothermal system of reduced W skarn deposits. 相似文献
18.
阳储岭斑岩型W-Mo矿床位于江南造山带中部,是华南地区最早发现的斑岩型钨钼矿床。已探明WO3资源储量6.13万吨(平均品位0.2%),Mo资源储量1.69万吨(平均品位0.03%～0.06%),其成矿作用与中生代花岗质岩浆活动密切相关。区内发育早期花岗闪长岩和晚期二长花岗斑岩,钨矿体以细脉状和浸染状产于二长花岗斑岩体内,而花岗闪长岩内未见矿化。两期岩浆活动与钨成矿的关系尚不明确,制约其含矿差异性的因素尚不清楚。本文以花岗闪长岩和二长花岗斑岩中的黑云母为研究对象,对比研究两类岩浆结晶分异程度、氧逸度、岩浆流体卤素浓度,探讨其对钨成矿的制约。黑云母主量元素分析结果显示,阳储岭两类岩浆岩均为壳源,但显著不同于S型花岗岩的Mg/(Fe+Mg)和AlVI值,指示其具有I型花岗岩的特征。黑云母的微量元素信息显示,相对于花岗闪长岩中的黑云母(类型一),二长花岗斑岩中的黑云母(类型二)显示低的K/Rb、Nb/Ta比值,高的Rb、Cs、Nb和Ta含量,表明其分异程度较花岗闪长岩更高,更有利于钨的富集。两类黑云母所指示的岩浆氧逸度均在NNO缓冲线附近,表明其母岩... 相似文献
19.
Extensive Early Cretaceous post-collisional igneous rocks, especially the large volume of granitoids developed in the Dabie orogen. Some of these granitic rocks are spatially, temporally, and genetically associated with economically important molybdenum deposits. The Tangjiaping large-scale (> 0.1 million ton) porphyry Mo deposit is located in the northwest of the Northern Dabie Complex unit. The Mo mineralization is mainly hosted in molybdenite-bearing quartz veinlets and stockworks in the Tangjiaping granite porphyry, which intruded into Proterozoic biotite-plagioclase gneiss and amphibole-plagioclase gneiss. Two alteration zones from the porphyry centre outwards and downwards can be recognized: (1) K-silicate alteration-silicification zone; (2) silicification-phyllic alteration zone. The Tangjiaping ore-bearing granite porphyry occurs as an individual stock with an outcrop of 0.4 km2. LA-ICP-MS zircon U-Pb dating of the Tangjiaping granite porphyry yields crystallization age of 115 ± 1 Ma, which is consistent with the molybdenite Re-Os age of the deposit given by previous studies. The Tangjiaping granitic rocks are metaluminous and belong to high-K calc-alkaline and shoshonitic series. They are relatively enriched in light rare earth elements and have moderately negative Eu anomalies. Geochemical and mineralogical characteristics indicate that the Tangjiaping granite is an A-type granite and was generated by partial melting of intermediate-felsic rocks at pressures of ca. 0.4–0.8 GPa. There are high initial 87Sr/86Sr ratios ranging from 0.707367 to 0.709410 and negative εNd(t) values varying from − 15.0 to − 14.2 for the Tangjiaping granite. In situ zircon Hf isotopic analyses show that the εHf(t) values of zircons from the Tangjiaping granite porphyry vary from − 17.0 to − 6.0. The geochemical data and Sr-Nd-Hf isotopes, coupled with the Neoproterozoic inherited zircon age (652 ± 21 Ma), indicate that the Tangjiaping granite porphyry was most likely derived from partial melting of the Northern Dabie gneiss with some relatively enriched mantle materials involved. The Tangjiaping Mo ore-forming granite porphyry was formed in an extensional setting. The Early Cretaceous asthenospheric upwelling might have played an important role in the formation of the approximately coeval Mo-bearing magmas in the Dabie orogen. 相似文献
20.
Lai-min Zhu Guo-wei Zhang Yan-jing Chen Zhen-ju Ding Bo Guo Fei Wang Ben Lee 《Ore Geology Reviews》2011,39(1-2):46-62
East Qinling is the largest porphyry molybdenum province in the world; these Mo deposits have been well documented. In West Qinling, however, few Mo deposits have been discovered although granitic rocks are widespread. Recently, the Wenquan porphyry Mo deposit has been discovered in Gansu province, which provides an insight into Mo mineralization in West Qinling. In this paper we report Pb isotope compositions for K-feldspar and sulfides, S isotope ratios for sulfides, the results obtained from petrochemical study and from in situ LA-ICP-MS zircon U-Pb dating and Hf isotopes. The granitoids are enriched in LILE and LREE, with REE and trace element patterns similar to continental crust, suggesting a crustal origin. The Mg# (40.05 to 56.34) and Cr and Ni contents are high, indicating a source of refractory mafic lower crust. The εHf(t) values of zircon grains from porphyritic monzogranite range from ? 2.9 to 0.6, and from granitic porphyry vary from ? 3.3 to 1.9. The zircons have TDM2 of 1014 to 1196 Ma for the porphyritic monzogranite and 954 to 1224 Ma for the granitic porphyry, implying that these granitoids were likely derived from partial melting of a Late Mesoproterozoic juvenile lower crust. The Pb isotope compositions of the granitoids are similar to granites in South China, showing that the magma was sourced from the middle–lower crust in the southern Qinling tectonic unit. The Pb isotopic contrast between the Mo-bearing granitoids and ores shows that the Pb in the ore-forming solution was derived from fractionation of a Triassic magmatic system. δ34S values of sulfides are between 5.02 and 5.66‰, similar to those associated with magmatic-hydrothermal systems. LA-ICP-MS zircon U-Pb dating yields crystallization ages of 216.2 ± 1.7 and 217.2 ± 2.0 Ma for the granitoids, consistent with a previously reported molybdenite Re-Os isochron age of 214.4 ± 7.1 Ma. This suggests that the Mo mineralization is related to the late Triassic magmatism in the West Qinling orogenic belt. In view of these geochemical results and known regional geology, we propose that both granitoid emplacement and Mo mineralization in the Wenquan deposit resulted from the Triassic collision between the South Qinling and the South China Block, along the Mianlue suture. Since Triassic granitoid plutons commonly occur along the Qinling orogenic belt, the Triassic Wenquan Mo-bearing granitoids highlight the importance of the Triassic tectono-magmatic belt for Mo exploration. In order to apply this metallogenic model to the whole Qinling orogen, further study is needed to compare the Wenquan deposit with other deposits. 相似文献