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1.
The late Triassic Baolun gold deposit hosted by Silurian phyllites is a large‐scale high‐grade gold deposit in Hainan Island, South China. The ores can be classified into quartz‐vein dominated type and less altered rock type. Three mineralization stages were recognized by mineral assemblages. The early stage, as the most important mineralization stage, is characterized by a quartz–native gold assemblage. The muscovite?quartz?pyrite?native gold assemblage is related to the intermedium mineralization stage. In late mineralization stage, native gold and Bi‐bearing minerals are paragenetic minerals. Microthermometry analyses show that the early mineralization stage is characterized by two types of fluid inclusions, including CO2‐rich inclusions (C‐type) and aqueous inclusions (W‐type). C‐type inclusions homogenize at 276–335°C with an averaged value of 306°C and have salinities of 1.0–10.0 wt% NaCl equivalent (mean value of 4.9 wt% NaCl equivalent). W‐type inclusions homogenize at 252–301°C (mean value of 278°C) with salinity of 4.0–9.7 wt% NaCl equivalent (mean value of 7.4 wt% NaCl equivalent). In intermedium mineralization stage, C‐type and W‐type inclusions homogenize at 228–320°C (mean value of 283°C) and 178–296°C (mean value of 241°C), with salinities of 2.4–9.9 wt% NaCl equivalent (mean value of 6.5 wt% NaCl equivalent) and 3.7–11.7 wt% NaCl equivalent (mean value of 7.7 wt% NaCl equivalent), respectively. No suitable mineral, such as quartz or calcite, was found for fluid inclusion study from late mineralization stage. In contrast, only aqueous inclusions were found from post‐ore barren veins, which yielded lower homogenization temperatures ranging from 168–241°C (mean value of 195°C) and similar salinities (2.6–12.6 wt% NaCl equivalent with averaged value of 7.2 wt% NaCl equivalent). The different homogenization temperatures and similar salinities of C‐type and W‐type from each mineralization stage indicate that fluid immiscibility and boiling occurred. The Baolun gold deposit was precipitated from a CO2‐bearing mesothermal fluid, and formed at a syn‐collision environment following the closure of the Paleo‐Tethys.  相似文献   

2.
The Mallery Lake area contains pristine examples of ancient precious metal-bearing low-sulfidation epithermal deposits. The deposits are hosted by rhyolitic flows of the Early Proterozoic Pitz Formation, but are themselves apparently of Middle Proterozoic age. Gold mineralization occurs in stockwork quartz veins that cut the rhyolites, and highest gold grades (up to 24 g/t over 30 cm) occur in the Chalcedonic Stockwork Zone. Quartz veining occurs in two main types: barren A veins, characterized by fine- to coarse-grained comb quartz, with fluorite, calcite, and/or adularia; and mineralized B veins, characterized by banded chalcedonic silica and fine-grained quartz, locally intergrown with fine-grained gold or electrum. A third type of quartz vein (C), which crosscuts B veins at one locality, is characterized by microcrystalline quartz intergrown with fine-grained hematite and rare electrum. Fluid inclusions in the veins occur in two distinct assemblages. Assemblage 1 inclusions represent a moderate temperature (Th=150 to 220 °C), low salinity (~1 eq. wt% NaCl, with trace CO2), locally boiling fluid; this fluid type is found in both A and B veins and is thought to have been responsible for Au-Ag transport and deposition. Assemblage 2 inclusions represent a lower temperature (Th=90 to 150 °C), high salinity calcic brine (23 to 31 wt% CaCl2-NaCl), which occurs as primary inclusions only in the barren A veins. Assemblage 1 and 2 inclusions occur in alternating quartz growth bands in the A-type veins, where they appear to represent alternating fluxes of dilute fluid and local saline groundwater. No workable primary fluid inclusions were observed in the C veins. The A-vein quartz yields '18O values from 8.3 to 14.5‰ (average=10.9ǃ.7‰ [1C], n=30), whereas '18O values for B-vein quartz range from 11.2 to 14.0‰ (average=13.0ǂ.9‰, n=12). Calculated '18OH2O values for the dilute mineralizing fluid from B veins range from -2.6 to 0.2‰ (average=-0.8ǂ.9‰, n=12) and are consistent with a dominantly meteoric origin. No values could be calculated for the brine, however, because all A-vein quartz samples contain mixed fluid inclusion populations. However, the fact that A-vein quartz samples extend to lower '18O values than the B veins suggests that the brine had a lighter isotopic signature relative to the dilute fluid. Hydrogen isotopic ratios of fluid inclusion waters extracted from eleven quartz samples of both vein types range from 'DFI=-56 to -134‰, but show no particular correlation with vein type. In most respects, the mineralogical and fluid characteristics of the Mallery Lake system are comparable to those of Phanerozoic low-sulfidation deposits, and although the presence of high salinity brines is unusual in such deposits, it is not unknown (e.g., Creede, Colorado). In addition, one of the few other examples of well-preserved, Precambrian, low-sulfidation epithermal deposits, from the Central Pilbara tectonic zone, Australia, contains a similarly bimodal fluid assemblage. The significance of these saline brines is not clear, but from this study we infer that they were not directly involved with Au-Ag transport or deposition.  相似文献   

3.
The Darreh‐Zereshk (DZ) and Ali‐Abad (AB) porphyry copper deposits are located in southwest of the Yazd city, central Iran. These deposits occur in granitoid intrusions, ranging in composition from quartz monzodiorite through granodiorite to granite. The ore‐hosting intrusions exhibit intense hydrofracturing that lead to the formation of quartz‐sulfide veinlets. Fluid inclusions in hydrothermal quartz in these deposits are classified as a mono‐phase vapor type (Type I), liquid‐rich two phase (liquid + vapor) type (Type IIA), vapor‐rich two phase (vapor + liquid) type (Type IIB), and multi‐phase (liquid + vapor + halite + sylvite + hematite + chalcopyrite and pyrite) type (Types III). Homogenization temperatures (Th) and salinity data are presented for fluid inclusions from hydrothermal quartz veinlets associated with potassic alteration and other varieties of hypogene mineralization. Ore precipitation occurred between 150° to >600°C from low to very high salinity (1.1–73.9 wt% NaCl equivalent) aqueous fluids. Two stages of hydrothermal activity characterized are recognized; one which shows relatively high Th and lower salinity fluid (Type IIIa; Th(L‐V) > Tm(NaCl)); and one which shows lower Th and higher salinity (Type IIIb; Th(L‐V) < Tm(NaCl)). The high Th(L‐V) and salinities of Type IIIa inclusions are interpreted to represent the initial existence of a dense fluid of magmatic origin. The coexistence of Type IIIb, Type I and Type IIB fluid inclusions suggest that these inclusions resulted either from trapping of boiling fluids and/or represent two immiscible fluids. These processes probably occurred as the result of pressure fluctuations from lithostatic to hydrostatic conditions under a pressure of 200 to 300 bar. Dilution of these early fluids by meteoritic water resulted in lower temperatures and low to moderate salinity (<20 wt% NaCl equiv.) fluids (Type IIA). Fluid inclusion analysis reveals that the hydrothermal fluid, which formed mineralized quartz veinlets in the rocks with potassic alteration, had temperatures of ~500°C and salinity ~50 wt% NaCl equiv. Cryogenic SEM‐EDS analyses of frozen and decrepitated ore‐bearing fluids trapped in the inclusions indicate the fluids were dominated with NaCl, and KCl with minor CaCl2.  相似文献   

4.
Gold ore-forming fluids of the Tanami region, Northern Australia   总被引:1,自引:0,他引:1  
Fluid inclusion studies have been carried out on major gold deposits and prospects in the Tanami region to determine the compositions of the associated fluids and the processes responsible for gold mineralization. Pre-ore, milky quartz veins contain only two-phase aqueous inclusions with salinities ≤19 wt% NaCl eq. and homogenization temperatures that range from 110 to 410°C. In contrast, the ore-bearing veins typically contain low to moderate salinity (<14 wt% NaCl eq.), H2O + CO2 ± CH4 ± N2-bearing fluids. The CO2-bearing inclusions coexist with two-phase aqueous inclusions that exhibit a wider range of salinities (≤21 wt% NaCl eq.). Post-ore quartz and carbonate veins contain mainly two-phase aqueous inclusions, with a last generation of aqueous inclusions being very CaCl2-rich. Salinities range from 7 to 33 wt% NaCl eq. and homogenization temperatures vary from 62 to 312°C. Gold deposits in the Tanami region are hosted by carbonaceous or iron-rich sedimentary rocks and/or mafic rocks. They formed over a range of depths at temperatures from 200 to 430°C. The Groundrush deposit formed at the greatest temperatures and depths (260–430°C and ≤11 km), whereas deposits in the Tanami goldfield formed at the lowest temperatures (≥200°C) and at the shallowest depths (1.5–5.6 km). There is also evidence in the Tanami goldfield for late-stage isothermal mixing with higher salinity (≤21 wt% NaCl eq.) fluids at temperatures between 100 and 200°C. Other deposits (e.g., The Granites, Callie, and Coyote) formed at intermediate depths and at temperatures ranging from 240 to 360°C. All ore fluids contained CO2 ± N2 ± CH4, with the more deeply formed deposits being enriched in CH4 and higher level deposits being enriched in CO2. Fluids from deposits hosted mainly by sedimentary rocks generally contained appreciable quantities of N2. The one exception is the Tanami goldfield, where the quartz veins were dominated by aqueous inclusions with rare CO2-bearing inclusions. Calculated δ 18O values for the ore fluids range from 3.8 to 8.5‰ and the corresponding δD values range from −89 to −37‰. Measured δ 13C values from CO2 extracted from fluid inclusions ranged from −5.1 to −8.4‰. These data indicate a magmatic or mixed magmatic/metamorphic source for the ore fluids in the Tanami region. Interpretation of the fluid inclusion, alteration, and structural data suggests that mineralization may have occurred via a number of processes. Gold occurs in veins associated with brittle fracturing and other dilational structures, but in the larger deposits, there is also an association with iron-rich rocks or carbonaceous sediments, suggesting that both structural and chemical controls are important. The major mineralization process appears to be boiling/effervescence of a gas-rich fluid, which leads to partitioning of H2S into the vapor phase resulting in gold precipitation. However, some deposits also show evidence of desulfidation by fluid–rock interaction and/or reduction of the ore-fluid by fluid mixing. These latter processes are generally more prevalent in the higher crustal-level deposits.  相似文献   

5.
The Chehugou Mo–Cu deposit, located 56 km west of Chifeng, NE China, is hosted by Triassic granite porphyry. Molybdenite–chalcopyrite mineralization of the deposit mainly occurs as veinlets in stockwork ore and dissemination in breccia ore, and two ore‐bearing quartz veins crop out to the south of the granite porphyry stock. Based on crosscutting relationships and mineral paragenesis, three hydrothermal stages are identified: (i) quartz–pyrite–molybdenite ± chalcopyrite stage; (ii) pyrite–quartz ± sphalerite stage; and (iii) quartz–calcite ± pyrite ± fluorite stage. Three types of fluid inclusions in the stockwork and breccia ore are recognized: LV, two‐phase aqueous inclusions (liquid‐rich); LVS, three‐phase liquid, vapor, and salt daughter crystal inclusions; and VL, two‐phase aqueous inclusions (gas‐rich). LV and LVS fluid inclusions are recognized in vein ore. Microthermometric investigation of the three types of fluid inclusions in hydrothermal quartz from the stockwork, breccia, and vein ores shows salinities from 1.57 to 66.75 wt% NaCl equivalents, with homogenization temperatures varying from 114°C to 550°C. The temperature changed from 282–550°C, 220–318°C to 114–243°C from the first stage to the third stage. The homogenization temperatures and salinity of the LV, LVS and VL inclusions are 114–442°C and 1.57–14.25 wt% NaCl equivalent, 301–550°C and 31.01–66.75 wt% NaCl equivalent, 286–420°C and 4.65–11.1 wt% NaCl equivalent, respectively. The VL inclusions coexist with the LV and LVS, which homogenize at the similar temperature. The above evidence shows that fluid‐boiling occurred in the ore‐forming stage. δ34S values of sulfide from three type ores change from ?0.61‰ to 0.86‰. These δ34S values of sulfide are similar to δ34S values of typical magmatic sulfide sulfur (c. 0‰), suggesting that ore‐forming materials are magmatic in origin.  相似文献   

6.
Gold-bearing quartz veins of the Taihua Group consisting of Archean metavolcanic rocks are a main gold deposit type in the Xiao Qinling area,one of the three biggest gold production areas in China.The quartz veins experienced strong alteration characterized by a typical mesothermal hydrothermal altered mineral assemblage.The grade of gold is affected by the contents of sulphides,e.g.galena,pyrite and chalcopyrite.Results of minor elements analysis for the of gold-bearing quartz veins indicate higher contents of Au and high contents of Ag,Pb,Cu,Cd,W,and Mo.Abundant fluid inclusions were found in the gold-bearing quartz veins.Three types of fluid inclusions were identified:(1) aqueous inclusions;(2) CO 2-bearing inclusions;and(3) daughter crystal-bearing fluid inclusions.Homogenization temperatures ranged from 110 to 670℃ with low and high peaks appearing at 160 180℃ and 280 300℃,respectively.The salinity of aqueous inclusions varies between 1.8 wt% and 38.2 wt% NaCl.The homogenization temperature and salinity show a positive correlation.The H and O isotopes of fluid inclusions in the gold-bearing quartz veins indicate that magmatic solution and metamorphic hydrothermal solution,together with meteoric water,were involved in the formation of gold-bearing fluid.Mesozoic magma activities related to granite intrusions should be the main source of CO 2 fluid with higher temperature and salinity.  相似文献   

7.
The tin‐ and tantalum‐bearing pegmatites of the Bynoe area are located in the western Pine Creek Geosyncline. They are emplaced within psammopelitic rocks in the contact aureole of the Two Sisters Granite. The latter is a Palaeoproterozoic, fractionated, granite with S‐type characteristics and comprises a syn‐ to late‐orogenic, variably foliated, medium‐grained biotite granite and a post‐orogenic, coarse‐grained biotite‐muscovite granite. The pegmatites comprise a border zone of fine grained muscovite + quartz followed inward by a wall zone of coarse grained muscovite + quartz which is in turn followed by an intermediate zone of quartz + feldspar + muscovite. A core zone of massive quartz is present in some occurrences. Feldspars in the intermediate zone are almost completely altered to kaolinite. This zone contains the bulk of cassiterite, tantalite and columbite mineralization. Fluid inclusions in pegmatitic quartz indicate that early Type A (CO2 + H2O ± CH4) inclusions were trapped at the H2O‐CO2 solvus at P~100 MPa, T~300°C (range 240–328°C) and salinity ~6 wt% eq NaCl. Pressure‐salinity corrected temperatures on Type B (H2O + ~20% vapour), C (H2O + < 15% vapour) and D (H2O + halite + vapour) inclusions also fall within the range of Type A inclusions. Oxygen and hydrogen isotope data show that kaolin was either formed in isotopic equilibrium with meteoric waters or subsequent to its formation, from hydrothermal fluid, underwent isotopic exchange with meteoric waters. Fluid inclusion waters from core zone quartz show enrichment in deuterium suggesting metamorphic influence. Isotope values on muscovite are consistent with a magmatic origin. It is suggested that the pegmatites were derived from the post‐orogenic phase of the Two Sisters Granite. Precipitation of cassiterite took place at about 300°C from an aqueous fluid largely as a result of increase in pH due to feldspar alteration.  相似文献   

8.
The Xihuashan tungsten deposit, Jiangxi province, China, is a world-class vein-type ore deposit hosted in Cambrian strata and Mesozoic granitic intrusions. There are two major sets of subparallel ore-bearing quartz veins. The ore mineral assemblage includes wolframite and molybdenite, with minor amounts of arsenopyrite, chalcopyrite, and pyrite. There are only two-phase aqueous-rich inclusions in wolframite but at least three major types of inclusions in quartz: two- or three-phase CO2-rich inclusions, two-phase pure CO2 inclusions and two-phase aqueous inclusions, indicating boiling. Fluid inclusions in wolframite have relatively higher homogenization temperatures and salinities (239–380°C, 3.8–13.7 wt.% NaCl equiv) compared with those in quartz (177–329°C, 0.9–8.1 wt.% NaCl equiv). These distinct differences suggest that those conventional microthermometric data from quartz are not adequate to explain the ore formation process. Enthalpy–salinity plot shows a linear relationship, implying mixing of different sources of fluids. Although boiling occurred during vein-type mineralization, it seems negligible for wolframite deposition. Mixing is the dominant mechanism of wolframite precipitation in Xihuashan. δ34S values of the sulfides range from −1.6 to +0.1‰, indicative of a magmatic source of sulfur. δ18O values of wolframite are relatively homogeneous, ranging from +4.8‰ to +6.3‰. Oxygen isotope modeling of boiling and mixing processes also indicates that mixing of two different fluids was an important mechanism in the precipitation of wolframite.  相似文献   

9.
The Bismark deposit (8.5 Mt at 8% Zn, 0.5% Pb, 0.2% Cu, and 50 g/t Ag) located in northern Mexico is an example of a stock-contact skarn end member of a continuum of deposit types collectively called high-temperature, carbonate-replacement deposits. The deposit is hosted by massive sulfide within altered limestone adjacent to the Bismark quartz monzonite stock (~42 Ma) and the Bismark fault. Alteration concurrently developed in both the intrusion and limestone. The former contains early potassic alteration comprising K-feldspar and biotite, which was overprinted by kaolinite-rich veins and alteration and later quartz, sericite, and pyrite with minor sphalerite and chalcopyrite. Prograde exoskarn alteration in the limestone consists of green andradite and diopside, and transitional skarn comprising red-brown andradite, green hedenbergite and minor vesuvinite, calcite, fluorite, and quartz. The main ore stage post-dates calc-silicate minerals and comprises sphalerite and galena with gangue pyrite, pyrrhotite, calcite, fluorite, and quartz. The entire hydrothermal system developed synchronously with faulting. Fluid inclusion studies reveal several distinct temporal, compositional, and thermal populations in pre-, syn- and post-ore quartz, fluorite, and calcite. The earliest primary fluid inclusions are coexisting vapor-rich (type 2A) and halite-bearing (type 3A; type 3B contain sylvite) brine inclusions (32 to >60 total wt% salts) that occur in pre-ore fluorite. Trapping temperatures are estimated to have been in excess of 400 °C under lithostatic pressures of ~450 bar (~1.5 km depth). Primary fluid inclusions trapped in syn-ore quartz display critical to near critical behavior (type 1C), have moderate salinity (8.4 to 10.9 wt% NaCl equiv.) and homogenization temperatures (Th) ranging from 351 to 438 °C. Liquid-rich type 1A and 1B (calcite-bearing) inclusions occur as primary to secondary inclusions predominantly in fluorite and show a range in Th (104–336 °C) and salinity (2.7–11.8 wt% NaCl equiv.), which at the higher Th and salinity ranges overlap with type 1C inclusions. Oxygen isotope analysis was carried out on garnet, quartz, and calcite (plus carbon isotopes) in pre-, syn-, post-ore, and peripheral veins. Pre-ore skarn related garnets have a δ18Omineral range between 3.9 and 8.4‰. Quartz from the main ore stage range between 13.6 and 16.0‰. Calcite from the main ore stage has δ13C values of –2.9 to –5.1‰ and δ18O values of 12.3 to 14.1‰, which are clearly distinct from post-ore veins and peripheral prospects that have much higher δ18O (16.6–27.3‰) and δ13C (1.3–3.1‰) values. Despite the numerous fluid inclusion types, only two fluid sources can be inferred, namely a magmatic fluid and an external fluid that equilibrated with limestone. Furthermore, isotopic data does not indicate any significant mixing between the two fluids, although fluid inclusion data may be interpreted otherwise. Thus, the various fluid types were likely to have formed from varying pressure–temperature conditions through faulting during exsolution of magmatic fluids. Late-stage hydrothermal fluid activity was dominated by the non-magmatic fluids and was post-ore.  相似文献   

10.
黑龙江省黑河市北大沟金矿床流体包裹体研究   总被引:1,自引:1,他引:0  
黑龙江省黑河市北大沟金矿床是近年来在大兴安岭燕山期成矿带发现的小型金矿床。对石英脉中流体包裹体岩相学研究、显微测温和气液相成分分析表明:(1)主成矿阶段石英脉中发育纯液相、气液两相、富气相和纯气相4类包裹体。(2)流体包裹体均一温度在160~380℃之间,主要集中在260~300℃;成矿流体为NaCl-H2O体系;流体包裹体盐度估计在0.2%~2.0%(NaCleq)之间;成矿流体密度估计在0.550~0.912 g/cm3之间;成矿压力估计在6×105~210×105Pa之间;估算成矿深度为0.06~2.10 km。(3)从流体包裹体成分分析获得的pH值为6.6~6.7之间,还原参数n(CH4+CO+H2)/n(CO2)(摩尔数比值)在0.027~0.271之间,表明具有浅成中偏酸性和弱还原环境成矿的特点。该矿床是与火山热液有关的浅成中—低温热液金矿床。  相似文献   

11.
Homogenization temperatures and salinity data are presented for fluid inclusions from hydrothermal gangue minerals (quartz and fluorite) associated with porphyry wolframite-molybdenite-arsenopyrite-sphaleritebismuth-chalcopyrite-cassiterite mineralization within the Fire Tower ore zone, Mt Pleasant, New Brunswick. The data indicate that ore mineral precipitation occurred within a temperature range of 260° to 490°C from moderate to high salinity (10–42 wt% NaCl equivalent) aqueous fluids. Two stages of hydrothermal activity characterized by high (>30 wt% NaCl equivalent) salinity fluids are recognized; one which occurred at relatively high temperature (350°–490°C); and one which took place at lower temperature (180°–250°C). The high salinity, high temperature stage is interpreted to be the result of resurgent boiling. Dilution of these early fluids by convecting meteoric water resulted in low to moderate salinity fluids, which dominate the inclusion population. The low temperature, high salinity fluid inclusions are interpreted to represent late residual fluids derived from boiling which occurred as a result of a change in the pressure regime from dominantly lithostatic to hydrostatic conditions.  相似文献   

12.
Homogenization temperature and salinity were determined for fluid inclusions in mostly quartz and partly sphalerite, cassiterite, and barite from the 28 tin-polymetallic ore deposits in Bolivia. Generally, the homogenization temperatures and salinities of these fluid inclusions are comparatively high for ore deposits formed by cassiterite mineralization, such as Morococala and Avicaya in the Oruro district, frequently indicating a temperature higher than 300°C and salinity higher than 20 equiv. wt% NaCl. Particularly, it is quite possible that tin deposits associated with the W-Bi and tourmaline mineralizations such as Viloco and Caracoles have been produced by such high-temperature hypersaline fluid ranging up to 500°C and 56 equiv. wt% NaCl, similar to the porphyry copper type. This feature reveals that the hydrothermal fluid related to the Sn-W-Bi mineralization may be of magmatic origin. Homogenization temperatures for the Pb-Zn deposits with no tin minerals are low, mostly ranging 170°–300°C. At the Avicaya-Bolivar mining area in the Oruro district as well as at the Tasna and Chocaya-Animas mining areas in the Quechisla district temperature gradients consistent with the zonal distributions of ore minerals were confirmed.  相似文献   

13.
Fluid inclusions in the gold-bearing quartz veins at the Um Rus area are of three types: H2O, H2O−CO2 and CO2 inclusions. H2O inclusions are the most abundant, they include two phases which exhibit low and high homogenization temperatures ranging from 150 to 200°C and 175 to 250°C, respectively. The salinity of aqueous inclusions, based on ice melting, varies between 6.1 and 8 equiv. wt% NaCl. On the other hand, H2O−CO2 fluid inclusions include three phases. Their total homogenization temperatures range from 270 to 325°C, and their salinity, based on clathrate melting, ranges between 0.8 and 3.8 equiv. wt% NaCl. CO2 fluid inclusions homogenize to a liquid phase and exhibit a low density range from 0.52 to 0.66 g/cm3. The partial mixing of H2O−CO2 and salt H2O−NaCl fluid inclusions is the main source of fluids from which the other types of inclusions were derived. The gold-bearing quartz veins are believed to be of medium temperature hydrothermal convective origin.  相似文献   

14.
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   

15.
The Bilimoia deposit (2.23 Mt, 24 g/t Au), located in the eastern Central Mobile Belt of mainland Papua New Guinea, is composed of fault‐hosted, NW–NNW‐trending Irumafimpa–Kora and Judd–Upper Kora Au‐quartz veins hosted by Middle–Late Triassic basement that was metamorphosed to medium‐grade greenschist facies between Middle–Late Triassic and Early–Middle Jurassic. Mineralizing fluids were introduced during crustal thickening, rapid uplift, change of plate motions from oblique to orthogonal compression, active faulting and S3 and S4 events in an S1–S4 deformation sequence. The Bilimoia deposit is spatially and temporally related to I‐type, early intermediate to felsic and late mafic intrusions emplaced in Late Miocene (9–7 Ma). Hydrothermal alteration and associated mineralization is divided into 10 main paragenetic stages: (1) chlorite–epidote‐selvaged quartz–calcite–specularite vein; (2) local quartz–illite–pyrite alteration; (3) quartz–sericite–mariposite–fuchsite–pyrite wall‐rock alteration that delimits the bounding shears; (4) finely banded, colloform‐, crustiform‐ and cockade‐textured and drusy quartz ± early wolframite ± late adularia; (5) hematite; (6) pyrite; (7) quartz ± amethyst‐base metal sulfides; (8) quartz–chalcopyrite–bornite–Sn and Cu sulfides–Au tellurides and Te ± Bi ± Ag ± Cu ± Pb phases; (9) Fe ± Mn carbonates; and (10) supergene overprint. Fluid inclusions in stage 4 are characterized by low salinity (0.9–5.4 wt% NaCl equivalent), aqueous–carbonic fluids with total homogenization temperatures ranging from 210 to 330°C. Some of the inclusions that homogenized between 285 and 330°C host coexisting liquid‐ and vapor‐rich (including carbonic) phases, suggesting phase separation. Fluid inclusions in quartz intergrown with wolframite have low salinity (0.9–1.2 wt% NaCl equivalent), aqueous–carbonic fluids at 240–260°C, defining the latter’s depositional conditions. The ore fluids were derived from oxidized magmatic source initially contaminated by reduced basement rocks. Wall‐rock alteration and involvement of circulating meteoric waters were dominant during the first three stages and early part of stage 4. Stage 5 hematite was deposited as a result of stage 4 phase separation or entrainment of oxygenated groundwater. Gold is associated with Te‐ and Bi‐bearing minerals and mostly precipitated as gold‐tellurides during stage 8. Gold deposition occurred below 350°C due to a change in the sulfidation and oxidation state of the fluids, depressurization and decreasing temperature and activities of sulfur and tellurium. Bisulfides are considered to be the main Au‐transporting complexes. The Bilimoia deposit has affinities that are similar to many gold systems termed epizonal orogenic and intrusion‐related. The current data allow us to classify the Bilimoia deposit as a fault‐controlled, metamorphic‐hosted, intrusion‐related mesothermal to low sulfidation epithermal quartz–Au–Te–Bi vein system.  相似文献   

16.
甲玛铜多金属矿床位于西藏冈底斯斑岩铜矿带东段,是近年来勘探发现的超大型斑岩-矽卡岩型铜多金属矿床。通过冷热台显微观察与测温、扫描电镜、激光拉曼探针测试,对甲玛矿床各成矿阶段典型矿物的流体包裹体研究表明,成矿流体富含挥发分,临界相均一的流体来自岩浆超临界流体出溶,主成矿阶段具有沸腾包裹体组合特征,有机质包裹体荧光效应显著。显微测温结果显示,岩浆-热液阶段斑岩中石英斑晶的流体包裹体均一温度范围为250~540℃,含石盐子晶高盐度包裹体盐度范围为35~61(wt%)NaCl.eq,中等盐度的临界均一的气液包裹体盐度范围为3~29(wt%)NaCl.eq,岩浆期后热液阶段斑岩、角岩中石英脉的流体包裹体均一温度范围为210~410℃,盐度范围为33~41(wt%)NaCl.eq,与其不混溶共生的中低盐度气液两相流体包裹体盐度范围为5~25(wt%)NaCl.eq。矽卡岩阶段矿物均一温度范围为130~360℃,盐度范围为3~41(wt%)NaCl.eq,从岩浆热液过渡阶段到石英-硫化物阶段均一温度与盐度呈阶梯式降低趋势。斑岩体石英的流体包裹体中含有较多黄铜矿子矿物,岩浆结晶分异过程中已经具成矿元素的富集。激光拉曼探针测试结果显示,成矿早期至主成矿期矿物流体包裹体气相成分主要为CO2、CH4和N2,各阶段矿物流体包裹体气相成分具有继承性。成矿流体为高温度高盐度,富含CO2、CH4的流体。成矿流体主要源于岩浆,后期混有大气降水。当岩浆热液上升时因压力的突然释放造成高温含矿热流体发生减压沸腾,CO2和CH4等气体大量逃逸,导致成矿物质快速沉淀。矿床在成因上与岩浆-热液成矿作用密切相关。  相似文献   

17.
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   

18.
Kuh-I-Mond field in the Zagros foreland basin is a conventional heavy oil resource and is composed of fractured carbonates whose fractures were filled by calcite, dolomite, and anhydrite cements. Oil inclusions occurred within the fracture-fill cements indicate that fractures were open and played an active role during oil migration and charge. The highest measured values for secondary porosities belong to fractures in Asmari Formation, which is characterized by significant amounts of vug- and fracture-filling cements. Fractures facilitated fluid circulation and subsequently dissolution of allochems and high Mg carbonates. In contrast, fine-grained carbonate facies were less cemented, and thus, porosity enhancement by cement dissolution was insignificant. Temperature profiles of oil inclusions in the dolomite, calcite, and anhydrite minerals characterized by distinct variations in the homogenization temperatures (Th) that are divided into two ranges below 50°C in anhydrites and from 45°C to 125°C in dolomites and calcites. The lower Th ranges for anhydrite suggests that it may have formed at shallower burial depths during early to middle diagenesis. The oil inclusions display trend for increasing temperature downward which conform to Formation geothermal gradient. In other word, the decreasing trend of Th temperatures upward within Asmari Formation that can be observed in Th versus depth plot is consistent with the uplift events at Late Miocene time and later that caused removal of about 1,300 m of the crest of the Kuh-I-Mond anticline. Vitrinite reflectance data from source rock intervals in the field area do not support vertical migration of locally generated hydrocarbons into the Kuh-I-Mond accumulation, and long-distance lateral oil migration and charge from a source kitchen to the southwest is proposed. Vitrinite reflectance data from this dolomite and limestone reservoir suggest low maturation levels corresponding to paleotemperatures less than 50°C. The observed maturation level (<0.5% Ro) does not exceed values for simple burial maturation based on the estimated burial history. Also, homogenization temperatures from fluid inclusion populations in calcite and dolomites show expected good correlation with reflectance-derived temperatures. The Th data represent pore fluids became warmer and more saline during burial. As aqueous fluid inclusions in calcite veins were homogenized between 22°C and 90°C with a decrease in salinity from 22 to 18 eq.?wt.% NaCl. The Th values suggest a change in water composition and that dolomite and calcite cements might have precipitated from petroleum-derived fluids. The hydrocarbon fluid inclusions microthermometry data suggest that the reservoir was being filled by heavy black oils in reservoir during Cenozoic. Aqueous fluid inclusions hosted by calcite equant sparry/fossil cavity fills suggest low cementation temperatures (<45°C) and high salinities (19 eq.?wt.% NaCl), while those in dolostones are characterized by highly variable homogenization temperature (52°C to 125°C) and salinities (6.5 to 20 eq.?wt.% NaCl).  相似文献   

19.
Lianhuashan mine in South China represents a new type of tungsten ore which can be described as a porphyry tungsten deposit. It is associated with a quartz porphyry stock of Yenshanian age (about 70–135 m. y.). The ore occurs in zone surrounding the contact of the quartz porphyry with Jurassic sandstone and extends into both rock bodies. The ore occurs either as the matrix of breccia or in the form of a very fine network of cross cutting veinlets. The major tungsten minerals are wolframite and scheelite associated with sulfide minerals of Mo, Fe, Cu, Pb and cassiterite. The minerals are fine-grained. There is zoned alteration in the wall rocks. From the center of the quartz porphyry toward the wall rocks one finds: potassic alteration, silicification-sericitization, and chloritization. All these features are similar to those of porphyry copper mineralization. Fluid inclusion studies show three types of inclusion: liquid-rich (Type I), gas-rich (Type II), and polyphase with daughter minerals (Type III) fluid inclusions. The homogenization temperatures of Type I range from 210° to 380°C, with a salinity of 2–15 wt.% NaCl equiv., those of Type II from 270° to 420°C, and those of Type III from 240° to 400°C with a salinity of 31–33 wt.% NaCl equiv. The closely associated group of gas-rich and daughter mineral-bearing fluid inclusions homogenized at almost the same temperatures. Such results indicate boiling of oreforming fluids. These fluid inclusion data indicate that low salinity (Type I) and high salinity fluids (Type III) responsible for porpb yry copper deposits are the same as those for porphyry tungsten ore deposits. These observations suggest that the Lianhuashan tungsten ore deposit is a porphyry tungsten deposit and was formed by hydrothermal fluids similar to those responsible for the well-known porphyry copper deposits.  相似文献   

20.
The Antuoling Mo deposit is a major porphyry‐type deposit in the polymetallic metallogenic belt of the northern Taihang Mountains, China. The processes of mineralization in this deposit can be divided into three stages: an early quartz–pyrite stage, a middle quartz–polymetallic sulfide stage, and a late quartz–carbonate stage. Four types of primary fluid inclusions are found in the deposit: two‐phase aqueous inclusions, daughter‐mineral‐bearing multiphase inclusions, CO2–H2O inclusions, and pure CO2 inclusions. From the early to the late ore‐forming stages, the homogenization temperatures of the fluid inclusions are 300 to >500°C, 270–425°C, and 195–330°C, respectively, with salinities of up to 50.2 wt%, 5.3–47.3 wt%, and 2.2–10.4 wt% NaCl equivalent, revealing that the ore‐forming fluids changed from high temperature and high salinity to lower temperature and lower salinity. Moreover, based on the laser Raman spectra, the compositions of the fluid inclusions evolved from the NaCl–CO2–H2O to the NaCl–H2O system. The δ18OH2O and δD values of quartz in the deposit range from +3.9‰ to +7.0‰ and ?117.5‰ to ?134.2‰, respectively, reflecting the δD of local meteoric water after oxygen isotopic exchange with host rocks. The Pb isotope values of the sulfides (208Pb/204Pb, 36.320–37.428; 207Pb/204Pb, 15.210–15.495; 206Pb/204Pb, 16.366–17.822) indicate that the ore‐forming materials originated from a mixed upper mantle–lower crust source.  相似文献   

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