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The Qiman Tagh W-Sn ore belt is located in the westernmost sector of the East Kunlun Orogen, NW China. It has been recognized as a unique W-Sn belt that formed in the early Paleozoic and related to closure of the Proto-Tethys. To understand the evolution of ore-forming fluids and its relationship with the tectonic setting of East Kunlun Orogen, we report the results obtained from fluid inclusion and H-O isotopic studies of ores and quartz veins for the Qiman Tagh W-Sn ore belt. Mineralization in Qiman Tagh includes four stages characterized by quartz-cassiterite-wolframite assemblage stage 1, quartz ± scheelite assemblage stage 2, quartz-polymetallic sulfides stage 3, and ore-barren veins stage 4. The former two stages are conducive to mineralization, while the latter two stages are less important. The fluid inclusions are distinguished between CO 2 -H 2 O (C-type) and NaCl-H 2 O (W-type) in composition, containing a trace of CH 4 , N 2 , C 2 H 6 , SO 2 , and CO 3 2– . Cassiterite and quartz in stage 1, instead of wolframite, contain a great deal of C-type inclusions. All inclusions in minerals of stage 1 yield homogenization temperatures of 230.1–384.1 °C (peaking at 310–320 °C), with salinities lower than 14.76 wt% NaCl equiv. and bulk densities of 0.63–0.89 g/cm 3 . The stage 2 minerals contain both two types of inclusions, yielding homogenization temperatures of 183.4–335.9 °C (peaking at 280–290 °C), with salinities lower than 14.53 wt% NaCl equiv. and bulk densities of 0.66–0.97 g/cm 3 . Fluid inclusions in minerals of stages 3 and 4 are mainly W-type and homogenized at temperatures of 140.6–277.6 °C (peaking 210–220 °C), and 116.9–255.1 °C (peaking 160–170 °C), respectively. The H-O isotopic systematics shows that the fluids were dominated by magmatic water in stages 1 and 2, but by meteoric water in stages 3 and 4. Integrating all the geological and geochemical data, we conclude that the fluids forming the Qiman Tagh W-Sn ore belt evolved from granite-derived, CO 2 -rich and reducing, to meteoric water-dominated, CO 2 -poor and oxidizing. Fluid immiscibility, cooling and interaction with rocks are main mechanisms for metallic deposition. [ABSTRACT FROM AUTHOR]

The giant Zijinshan Cu-Au deposit in the Zijinshan orefield, Fujian Province, southeastern China, is the first high-sulfidation epithermal deposit identified in mainland China. The Cu and Au orebodies occur as veins and pods in the NW-trending faults and breccias zones. Intensive and pervasive alteration is characterized by downward and outward zoning from intensively leached silicic alteration (or vuggy quartz, Q), through alunite-quartz-pyrite alteration (advanced aragillic alteration, Q-Alu) and the quartz-alunite alteration overprinting the sericite alteration (Q-Alu-Di-Srt), to sericite (or phyllic) alteration zone. Gold mineralization mainly occurs in the silicic alteration zone, while the copper mineralization is confined in the alunite-quartz alteration zone. On the basis of detailed petrographic study, an early porphyry type mineralization stage, characterized by chalcopyrite-bornite-molybdenite-pyrite-sericite assemblage is recognized at Zijinshan, which is subsequently and strongly overprinted by the sulfate alteration and high-sulfidation Cu-Au mineralization stages. A supergene stage is also identified at shallow depth of the deposit, with gold largely enriched but copper commonly leached. The ore-forming fluids related to the early sericite alteration and possibly porphyry type mineralization are high-temperature, high-salinity magmatic water, characterized by the presence of the halite-bearing inclusions. The CO 2 -H 2 O (C-type) inclusions are mostly vapor-rich and abundantly identified in the samples with advance argillic alteration (alunite alteration). They are regarded to be the buoyant vapor phase by fluid boiling of a single-phase, low- to moderate-salinity magmatic fluid at depth, where a separated saline phase and related porphyry mineralization might be expected. A group of secondary inclusions coexisting with enargite grains are recognized in the samples with alunite alteration and suggested to be trapped from the ore-forming fluids of the Cu-Au mineralization stage. The total homogenization temperatures and salinities of the secondary inclusions are below 300 °C (peaking at 260–280 °C) and under 10 wt% NaCl eqv., respectively. Intensive fluid boiling is the major mechanism for the formation of the giant high-sulfidation Cu (covellite-, digenite-dominated) orebodies in the Zijinshan deposit. It is a deep-seated high-sulfidation epithermal deposit according to the estimated depth of 1.4–2.1 km from the C-type inclusions in quartz grains from the alunite alteration zone. By fluid inclusion mapping of a nearly NW-trending cross section profile, the isotherms are extrapolated using the average total homogenization temperatures and the possible heat source is suggested. It is indicated that the heat source and possible concealed porphyry mineralization nearly coeval to the high-sulfidation Cu-Au mineralization at Zijinshan might be located at the southeastern Zijinshan deposit or the northern area between the Zijinshan and Wuziqilong deposits, where deep drilling is encouraged. [ABSTRACT FROM AUTHOR]

The large Yueyang Ag-Au-Cu deposit is commonly regarded as a low-sulfidation epithermal deposit in the Zijinshan orefield, Fujian Province, southeastern China. The Ag-Ag-Cu orebodies hosted in the Zijinshan granitic batholith are mainly stratoid and lens in shape, and controlled by a series of NW-trending listric faults with shallow dip angles. Four mineralization stages are recognized on the basis of mineral assemblage, ore fabrics, and crosscutting relationships of the ore veins, namely: pre-ore (pyrite + sericite + quartz ± chlorite), main Cu (chalcopyrite + pyrite + sericite + quartz ± bornite), main Ag-Au (Ag and Au minerals + pyrite + quartz + adularia ± calcite ± apatite ± chalcopyrite ± galena ± sphalerite) and post-ore (quartz ± chalcedony ± calcite) stages. Fluid inclusions (FIs) in the deposit include aqueous liquid-rich (WL-), aqueous vapor-rich (WV-), and minor carbonic (C-) and daughter mineral-bearing (S-) type ones. WL-subtype is the main inclusion type in the Yueyang deposit, accounting for more than 90% in proportion in each stage. Minor WV-subtype inclusions occur in both the main Cu and Ag stages, while the C-type and S-type ones are only observed in the main Cu stage. Fluid inclusion and H-O isotope study indicated that the ore-forming fluid of the main Cu stage is primarily magmatic vapor, which further underwent fluid boiling and mixing with meteoric water, while the ore-forming fluid of the main Ag stage is meteoric water-dominated, and the precipitation of silver and gold was mainly resulted from fluid boiling and the precipitation of other sulfides. On the basis of the aforementioned geological, fluid inclusion and stable isotope studies, we proposed a two-stage model for the Yueyang deposit, including a magmatic vapor-related porphyry type Cu mineralization and meteoric water-related low-sulfidation epithermal Ag-Au-Cu mineralization, although the porphyry Cu mineralization is very limited in scale. The mineralization and exhumation depths of the Yueyang deposit are estimated to be 448‒527 m and 18‒97 m, respectively. By comparison with the exhumation depths of other deposits in the Zijinshan orefield, it is suggested that more epithermal deposits could be found in the southwest of the orefield due to less uplift and exhumation therein. [ABSTRACT FROM AUTHOR]

The Qiangma gold deposit is hosted in the > 1.9 Ga Taihua Supergroup metamorphic rocks in the Xiaoqinling terrane, Qinling Orogen, on the southern margin of the North China Craton. The mineralization can be divided as follows: quartz-pyrite veins early, quartz-polymetallic sulfide veinlets middle, and carbonate-quartz veinlets late stages, with gold being mainly introduced in the middle stage. Three types of fluid inclusions were identified based on petrography and laser Raman spectroscopy, i.e., pure carbonic, carbonic-aqueous (CO 2 –H 2 O) and aqueous inclusions. The early-stage quartz contains pure carbonic and CO 2 –H 2 O inclusions with salinities up to 12.7 wt.% NaCl equiv., bulk densities of 0.67 to 0.86 g/cm 3 , and homogenization temperatures of 280−365 °C. The early-stage is related to H 2 O–CO 2 ± N 2 ± CH 4 fluids with isotopic signatures consistent with a metamorphic origin (δ 18 O water = 3.1 to 5.2‰, δD = − 37 to − 73‰). The middle-stage quartz contains all three types of fluid inclusions, of which the CO 2 –H 2 O and aqueous inclusions yield homogenization temperatures of 249−346 °C and 230−345 °C, respectively. The CO 2 –H 2 O inclusions have salinities up to 10.9 wt.% NaCl equiv. and bulk densities of 0.70 to 0.98 g/cm 3 , with vapor bubbles composed of CO 2 and N 2 . The isotopic ratios (δ 18 O water = 2.2 to 3.6‰, δD = − 47 to − 79‰) suggest that the middle-stage fluids were mixed by metamorphic and meteoric fluids. In the late-stage quartz only the aqueous inclusions are observed, which have low salinities (0.9−9.9 wt.% NaCl equiv.) and low homogenization temperatures (145−223 °C). The isotopic composition (δ 18 O water = − 1.9 to 0.5‰, δD = − 55 to − 66‰) indicates the late-stage fluids were mainly meteoric water. Trapping pressures estimated from CO 2 –H 2 O inclusions are 100−285 MPa for the middle stage, suggesting that gold mineralization mainly occurred at depths of 10 km. Fluid boiling and mixing caused rapid precipitation of sulfides and native Au. Through boiling and inflow of meteoric water, the ore-forming fluid system evolved from CO 2 -rich to CO 2 -poor in composition, and from metamorphic to meteoric, as indicated by decreasing δ 18 O water values from early to late. The carbon, sulfur and lead isotope compositions suggest the hostrocks within the Taihua Supergroup to be a significant source of ore metals. Integrating the data obtained from the studies including regional geology, ore geology, and fluid inclusion and C–H–O–S–Pb isotope geochemistry, we conclude that the Qiangma gold deposit was an orogenic-type system formed in the tectonic transition from compression to extension during the Jurassic−Early Cretaceous continental collision between the North China and Yangtze cratons. [ABSTRACT FROM AUTHOR]

The Donggou Mo deposit in the eastern Qinling area, China, is a giant porphyry system discovered based on a targeting concept by using the tectonic model for collisional orogeny, metallogeny and fluid flow (CMF model). Mo mineralization is associated with the Donggou aluminous A-type granite porphyry and was formed during the Early Cretaceous in a tectonic regime of continental extension. The orebodies mainly occur as numerous veinlets in the host-rocks. Hydrothermal ore-forming processes include at least three stages, characterized by veinlets of (1) quartz + K-feldspar + minor molybdenite, (2) quartz + molybdenite ± beryl and (3) quartz + carbonate + fluorite. Three types of fluid inclusions (FIs) are distinguished in quartz and beryl in stages 1 and 2, i.e., aqueous (W-type), carbonic–aqueous (C-type) and solid-bearing (S-type), with only aqueous FIs observed in stage 3 minerals. S-type FIs contain variable daughter minerals including halite, chalcopyrite, calcite and an unidentified transparent crystal, but only halite can dissolve during heating. Halite-bearing S-type FIs are mainly homogenized by halite dissolution at 182–416 °C, corresponding to salinities of 30.9–49.2 wt.% NaCl equiv.; minor halite-bearing S-type FIs are homogenized to liquid at 190–360 °C via vapor disappearance, with salinities of 29.1–36.2 wt.% NaCl equiv. Other FIs in minerals of stages 1, 2 and 3 are homogenized at temperatures of 341–550 °C, 220–440 °C and 125–225 °C, with salinities of 8.0–18.3, 5.3–16.8 and 0.5–7.3 wt.% NaCl equiv., respectively. The estimated minimum trapping pressures are up to 141 MPa in stage 1 and up to 81 MPa in stage 2, respectively, corresponding to an initial mineralization depth of no less than 5 km. The quartz in veinlets yields δ 18 O values of 8.5–10.0‰, corresponding to δ 18 O H 2 O values of − 2.9 to 5.9‰, while the δD H 2 O values of fluid inclusions range from − 59 to − 82‰. These data suggest that the ore fluids forming the Donggou deposit changed from high-temperature, high-salinity, CO 2 -rich magmatic to low-temperature, low-salinity and CO 2 -poor meteoritic fluids via boiling and mixing, resembling those of other magmatic–hydrothermal systems in Qinling Orogen and Dabie Shan. This supports the notion that the porphyry systems generated in a post-collisional tectonic setting were initially CO 2 -rich, as indicated by abundant C-type and CO 2 -bearing S-type fluid inclusions. [ABSTRACT FROM AUTHOR]

The East Qinling region in central China, hosting several tens of Mesozoic magmatic-hydrothermal Mo deposits, is one of the largest molybdenum belts in the world. The Zhifang Mo deposit is hosted in volcanic rocks of the Xiong'er Group in the Waifangshan area, Qinling Orogen. Previous studies variously correlated the mineralization in this deposit with Yanshanian magmatism or Palaeo-Mesoproterozoic volcanic-hydrothermal events. The orebodies are associated with quartz veins and controlled by subsidiary faults of the Machaoying Fault. The ore-forming process can be divided into the early, middle and late stages and is characterized by quartz-pyrite, quartz-polymetallic sulphide and quartz-carbonate veins, respectively. The early-stage quartz is structurally deformed, suggesting a compressional tectonic regime; the middle-stage sulphides fill the fractures of the early-stage assemblages and show no deformation, suggesting a tensional setting; the late-stage veins mostly infill the open-space fissures. Three types of fluid inclusions (FIs) are identified at the Zhifang deposit: H2O-NaCl (W-type), CO2-rich (C-type) and daughter mineral-bearing inclusions (S-type). Fluid inclusions of early-stage quartz homogenize between 380 and 470 °C, with salinities ranging from 0.4 to 9.6 wt.% NaCl equiv., whereas the late-stage calcite contains only the W-type FIs with homogenization temperatures of lower than 240 °C, and salinities of 0.4-8.7 wt.% NaCl equiv. This indicates that the ore fluid system evolved from CO2-rich, probably metamorphic hydrothermal to CO2-poor, meteoric fluid. All three types of FIs can be observed in the middle-stage quartz, and even in the microscopic domain of a crystal, suggesting that this heterogeneous association was trapped from a boiling fluid system. These FIs homogenized at temperatures ranging from 250 to 360 °C and display two salinity clusters of <18.5 and 29.1-29.9 wt.% NaCl equiv. These results suggest that metal precipitation resulted from fluid boiling. The estimated trapping pressures of FIs range from 101 to 285 MPa, suggesting an alternating lithostatic-hydrostatic fluid system, which was controlled by a fault-valve at the depth of 10 km. The δ34S values of ore minerals from the Zhifang Mo deposit show a range between −11.8‰ and 6.0‰, with a bimodal distribution. The early-stage pyrite has a positive δ34S value of 6.0‰ that is similar to the host rocks of the Xiong'er Group and the Taihua Supergroup, suggesting that the wall rocks contributed much of the sulphur to the early-stage pyrite during fluid-rock interaction. However, the δ34S values of the middle-stage sulphides have negative mean and restricted range from −11.8‰ to −4.5‰. The widespread rutile grains coexisting with molybdenite in the middle-stage correlate the negative δ34S values with relatively oxidized fluids. We consider phase separation as an efficient mechanism for ore-fluid oxidation and molybdenum deposition based on fluid inclusions and sulphur isotope data. Geological, fluid inclusion and sulphur isotope data of the Zhifang Mo deposit suggest that the Mo mineralization is unrelated to the Yanshanian magmatism or the Palaeo-Mesoproterozoic volcanic-hydrothermal event. Here we propose that the Zhifang Mo deposit may be considered as an orogenic mineral system, with its formation in an active continental margin related to the northward subduction of the Mian-Lue oceanic plate during the Triassic. Copyright © 2014 John Wiley & Sons, Ltd. [ABSTRACT FROM AUTHOR]

The Xunyang Hg-Sb orefield, Shaanxi Province, containing two large (Gongguan and Qingtonggou) and tens of small to medium Hg-Sb deposits, is located in the southern Qinling Orogen. Ore bodies of the deposits are hosted in Devonian dolomite and controlled by a fault system. Ores are mainly present as massive veins, disseminations, breccias and fine veinlets, with cinnabar (Hg) and stibnite (Sb) being the dominant ore minerals. Gangue minerals include quartz, calcite and dolomite. Hydrothermal minerals (quartz and calcite) only contain aqueous fluid inclusions with low homogenization temperature (135-274 °C) and salinity (1.23-12.3 wt.% NaCl equiv.), supporting an epizonogenic hydrothermal origin. The carbon, oxygen and hydrogen isotope data indicate that the ore-forming fluids were mainly sourced from epizonogenic to metamorphic devolatilization of the Sinian−Triassic strata that possibly underthrusted beneath the orefield, with inflow of the circulating meteoric water. Sulphur isotope ratios of stibnite and cinnabar range from 2‰ to 12‰, suggesting a contribution from sedimentary sulphate or sulphate-bearing fluids potted in strata, which is coincident with the δ34S values (3.4-8.6‰) of diagenetic pyrite in the strata. The conclusion drawn from sulphur isotopes is fully supported by the Pb isotope signatures. In addition, the 87Sr/86Sr ratios gradationally increase from ore-hosting dolostones, through ore-barren calcite or low-grade ores, to high-grade ores, indicating that a portion of the fluids originated from a source with higher 87Sr/86Sr values than the host-rocks, which is possibly composed of the Neoproterozoic−Lower Palaeozoic basement of the Xunyang Basin. Integrating the data from ore geology, fluid inclusion microthermometry and stable, radioactive isotope geochemistry, it can be concluded that the deposits in the Xunyang Hg-Sb orefield were formed by epizonogenic hydrothermal fluids mainly sourced from the strata via structural deformation during the North China−Yangtze continental collision. Copyright © 2014 John Wiley & Sons, Ltd. [ABSTRACT FROM AUTHOR]

The Wenyu giant gold deposit is hosted in the Precambrian Taihua Supergroup metamorphic rocks within the Xiaoqinling terrane (Qinling Orogen), on the southern margin of the North China Craton. The mineralization can be divided into three stages: quartz–pyrite veins early, quartz–sulfide veins middle (main), and carbonate–quartz veinlets late, with gold being mainly introduced in main stage. Quartz formed in two earlier stages contains three compositional types of fluid inclusions, i.e. pure CO2, CO2–H2O and NaCl–H2O, but the late-stage minerals only contain the NaCl–H2O inclusions. The inclusions in quartz formed in the early, main and late stages yield total homogenization temperatures of 262–417°C, 236–407°C and 114–239°C, respectively, with salinities no higher than 13wt.% NaCl equiv. Trapping pressures estimated from CO2–H2O inclusions are 139–399MPa and 111–316MPa in the early and main stages, corresponding to mineralization depths of 14km and 11km, respectively. Fluid boiling and mixing caused rapid precipitation of sulfides and native Au. Through boiling and inflow of meteoric water, the ore-forming fluid system evolved from CO2-rich to CO2-poor in composition, and from metamorphic to meteoric, as indicated by decreasing δ18Owater values from early to late. The carbon, sulfur and lead isotope compositions suggest the hostrocks within the Taihua Supergroup to be a significant source of ore metals. Integrating the data obtained from the studies including regional geology, ore geology, fluid inclusion and C–H–O–S–Pb isotope geochemistry, we conclude that the Wenyu gold deposit was an orogenic-type system formed in the tectonic transition from compression to extension during the Jurassic–Early Cretaceous continental collision between the North China and Yangtze Cratons. [ABSTRACT FROM AUTHOR]

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±1.0Ma, 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 62.9wt.% NaCl equiv., respectively. FIs of the middle-stage yield homogenization temperatures of 340 to 480°C and salinities of 0.5 to 56.0wt.% 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 8.4wt.% NaCl equiv. The minimum estimated pressures of the three stages are 30–70MPa, 10–40MPa and 1–10MPa, respectively, corresponding to minimum ore-forming depths of 1–2.8km. 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. [ABSTRACT FROM AUTHOR]

The Eastern Qinling, Central China, containing more than 20 Mesozoic porphyry±skarn systems, is the most important Mo province in the world. The Shangfanggou giant Mo deposit, Luanchuan County, Henan Province, is a porphyry-skarn system hosted in a lithologic association comprising carbonaceous sandstone, shale, carbonate and chert within the Neoproterozoic Luanchuan Group. Mo ores are mainly altered porphyry, skarn and hornfels, with minor altered gabbro. The mineralization process includes four stages, potassic alteration of the porphyry and skarnization of dolomite marble in stage 1, stockworks of quartz+molybdenite±sulfide (stage 2), pyrite+quartz±sulfides (stage 3), and carbonate±quartz±fluorite (stage 4), respectively. Mo mineralization was generally associated with strong silicification and/or phyllic alteration. The fluid inclusions in minerals include three compositional types, i.e., CO2-bearing (C-type), aqueous (W-type) and daughter mineral-bearing (S-type). Minerals formed in stages 1 to 3 contain all the three types of FIs, but the stage 4 minerals only contain the W-type FIs. Oxides and Cu-phosphate are recognized as daughter minerals in S-type inclusions in minerals of stage 1, whereas the daughter sulfide and reducing gases such as CO, CH4, H2S and C2H6 can be observed in quartz of stages 2 and 3, suggesting that the ore-forming fluids were initially oxidizing and then evolved to reducing. Boiling fluid inclusion assemblages can be observed in minerals formed in stage 2 or earlier, but not in stage 3 or later. Fluid boiling caused CO2 escape, oxygen fugacity decrease and rapid precipitation of ore minerals, and was a key factor causing Mo-mineralization at Shangfanggou. Data and interpretations presented in this contribution show that the fluids forming the Shangfanggou Mo deposit evolved from CO2-rich, high-salinity hypothermal, to CO2-poor, low-salinity epithermal (low-T). The Mo mineralization at the Shangfanggou deposit mainly occurred at depth of 6.6–7.0km, deeper than the majority of porphyry systems in volcanic arcs, which resulted from a CO2-rich magma–fluid system originating from partial melting of thickened lower crust. The Shangfanggou mineral system developed during 158–134Ma when the Yangtze–North China continental collision began to evolve from compression to extension. Magmatic hydrothermal deposits developed in a continental collision regime are generally formed by CO2-rich, high-salinity fluids. [ABSTRACT FROM AUTHOR]

The East Qinling Molybdenum Belt (EQMB), central China, hosting tens of Mesozoic magmatic hydrothermal Mo deposits, is one of the largest molybdenum belts in the world. Recently, a new type of Mo mineralization characterized by molybdenite-fluorite veins was discovered with ongoing prospecting at the Tumen area in the Huaxiong block, representing the southernmost tectonic unit of the North China Craton. The molybdenite-fluorite veins occur in faults or ductile shear zones cross-cutting the Neoproterozoic Luanchuan Group. At the Tumen deposit, CO2-rich, aqueous and daughter mineral-bearing fluid inclusions are observed in fluorite. These fluid inclusions resemble those reported from magmatic hydrothermal Mo systems formed in intracontinental tectonic settings and yield homogenization temperatures up to 450 °C, with salinities up to 39.8 wt.% NaCl equiv, suggesting that the mineralization resulted from a magmatic fluid system. Seven molybdenite analyses from the molybdenite-fluorite veins yield Re-Os isotope ages ranging from 845.8 ± 7.3 to 965.3 ± 7.2 Ma, with an isochron age of 847.4 ± 7.3 Ma (2 σ, MSWD = 23), marking the timing of mineralization as Neoproterozoic. These ages are broadly comparable with the 844.3 ± 1.6 Ma age reported from the Shuangshan syenite located near the mining area, and the ca. 830 Ma gabbros occurring within the same tectonic unit, indicating that the deposit was possibly related to Neoproterozoic rifting at the southern margin of the North China Craton. The age data correspond to the transition from the culmination of the assembly of the Neoproterozoic supercontinent Rodinia to the beginning of its break-up. Our results provide new insights into the regional tectonics and show that the Mo mineralization is not related to the much younger Mesozoic Yanshanian magmatism as considered in previous studies. Copyright © 2013 John Wiley & Sons, Ltd. [ABSTRACT FROM AUTHOR]

Abstract: The Qian''echong Mo deposit in Guangshan county, Henan Province, China, is a giant porphyry Mo deposit formed in Early Cretaceous in the Dabie Shan. Mo mineralization is associated with the Qian''echong granite porphyry, mainly presenting as numerous veinlets in the altered wallrocks, with potassic, phyllic, argillic and propylitic alteration developed. The hydrothermal ore-forming process can be divided into four stages: quartz+potassic feldspar+magnetite stage 1, quartz+molybdenite stage 2, quartz+carbonate+polymetal sulfide stage 3 and quartz+carbonate+fluorite stage 4. Fluid inclusions (FIs) can be distinguished between pure carbonic, carbonic, aqueous and solid-bearing types, but only the stage 1 quartz contains all the four types of FIs. The stage 2 quartz has three of the four types of FIs, with exception of PC-type. The stage 3 minerals are developed with the aqueous FIs with or without daughter minerals, but short of any kinds of CO2-bearing FIs. In stage 4 minerals, only the W-type FIs can be observed. The FIs in minerals of stages 1, 2 and 3 are mainly homogenized at temperatures of 260−400°C, 200−340°C and 160−300°C, with salinities of 2.00−11.58wt.% NaCl.eqv, 1.06−10.98wt.% NaCl.eqv and 0.53−9.47wt.% NaCl.eqv, respectively. The estimated minimum trapping pressures are up to 100MPa in stage 1 and to 62MPa in stage 2, respectively, corresponding to an initial mineralization depth of no less than 4km. The quartz separates from veinlets yield δ18O values of 7.1−10.2‰, corresponding to δ18OH2O values of −1.4−5.7‰, and the δDH2O values of fluid inclusions of −55−−72‰, suggesting that the ore-fluids evolved from magmatic to meteoric in sources. Therefore, the initial fluids forming the Qian''echong deposit, compared to those forming the porphyry systems in volcanic arcs, are characterized by relatively high temperature, high salinity, high fO2, CO2-rich, and NaCl-poor, considering that no halite has been observed in S-type FIs. We suggest that the “CO2-rich fluid” is a distinctive feature of porphyry systems developed in continental collision regime. [Copyright &y& Elsevier]

Abstract: The Wulasigou Cu deposit occurs as veins controlled by a NW-trending structure in a Devonian volcano-sedimentary basin of the Altay orogenic belt, Xinjiang, China. Igneous and sedimentary rocks exposed in the area have undergone greenschist-facies metamorphism. The ore-forming process can be divided into early, middle, and late stages, represented by, respectively, pyrite-quartz, polymetallic sulfide-quartz, and carbonate–quartz veins, veinlets, and/or replacement bodies. The early veins were deformed and brecciated during a compressional or transpressional event. The middle-stage veinlets filled fractures in the early-stage vein and alteration assemblages, and are undeformed, suggesting a tensional shear setting. The late-stage veinlets are mainly open-space fissure fillings that cut veins and replacement bodies formed in the earlier stages. Four types of fluid inclusions (FIs), including aqueous (W-type), mixed carbonic-aqueous (M-type), purely carbonic (C-type) and daughter mineral-bearing (S-type), have been identified in copper-related quartz and calcite from the Wulasigou deposit. The early-stage quartz contains M- and W-type primary FIs that completely homogenized at temperatures of 322–412°C with low salinities of 0.9–6.5wt.% NaCl equiv. In contrast, the late-stage quartz or calcite contains only the W-type FIs with homogenization temperatures of 101–234°C, and salinities of 0.9–2.9wt.% NaCl equiv. This indicates that the metallogenic system evolved from CO2-rich, metamorphic to CO2-poor, through input of meteoric fluids. All four types of FIs can only be observed in the middle-stage minerals, where they show evidence of vein formation during an episode of fluid immiscibility. These FIs homogenized at temperatures ranging mainly from 230 to 347°C, with salinities clustering 2.7–10.2wt.% NaCl equiv for the W-, M- and C-types, and 34.7–38.2wt.% NaCl equiv for the S-type, respectively. The metal precipitation resulted from a decrease in copper solubility during the fluid immiscibility episode. The estimated trapping pressures for the middle-stage fluids are 1.55–3.55kbar, suggesting an alternating lithostatic-hydrostatic fluid-system, controlled by fault-valve activity at a depth of 13–15.5km. Muscovite separates from the middle-stage polymetallic-quartz veinlets yield a well-defined 40Ar/39Ar isotopic plateau age of 219.41±2.10Ma, and an 39Ar/36Ar - 40Ar/36Ar isochron age of 219.73±2.17Ma. This age postdates the final Paleo-Asia Ocean closure (at ca. 250Ma) by about 30Ma, and indicates that the Cu mineralization at Wulasigou has occurred in the Triassic continental collision setting. Hence, the Wulasigou Cu deposit may be the first example of orogenic lode Cu deposits formed in accretionary orogeny or continental collision. [Copyright &y& Elsevier]

Abstract: The Nannihu Mo–W deposit, located in the Henan Province of China, is a giant porphyry deposit formed in the Qinling Orogen during the Jurassic continental collision between the North China and Yangtze Cratons. Mo–W mineralization is associated with the Nannihu porphyritic monzogranite, occurring as numerous stockwork veinlets in the altered wallrocks and the causative porphyry. Both the porphyry stock and wallrocks underwent intense hydrothermal alteration, ranging outwardly from potassic to phyllic alteration, and to carbonation zones with increasing distance from the intrusion. The hydrothermal ore-forming process can be divided into four stages characterized by veinlets, from early to late: (1) quartz+potassic feldspar±molybdenite±pyrite; (2) quartz+molybdenite veins containing minor pyrite and chalcopyrite; (3) quartz+polymetal sulfide; and (4) quartz+carbonate+fluorite. Most of the ores are formed during stages 2 and 3. Four types of fluid inclusions (FIs) are distinguished in this study based on petrographic and microthermometric criteria, i.e. pure CO2, NaCl–H2O, CO2–H2O and daughter mineral-bearing fluid inclusions. All of the four types of FIs can be observed in the hydrothermal quartz formed in stages 1, 2 and 3; while the stage 4 minerals contain only NaCl–H2O fluid inclusions. Fluid inclusions of stage 1 are mainly homogenized between 350 and 460°C, with salinities ranging from 5.7 to 17.9wt.% NaCl equiv. The stage 2 FIs yield homogeneous temperatures of 300–380°C and salinities of 3.5–16.9wt.% NaCl equiv. FIs of stage 3 are homogenized between 250 and 370°C, with salinities of 1.8–14.3 and 28.6–39.1wt.% NaCl equiv. FIs of stage 4 are homogenized at temperatures of 115 to 265°C, yielding salinities of 0.5 to 1.2wt.% NaCl equiv. Daughter minerals, such as halite, chalcopyrite and some unknown minerals, are frequently present in stage 3 FIs, which probably represent a reducing and oversaturated fluid-system resulting from fluid-boiling. The daughter mineral-bearing FIs coexist with vapor- and liquid-rich NaCl–H2O FIs that have contrasting salinities. These FIs are homogenized in divergent ways at similar temperatures, suggesting that fluid boiling took place in stages 2 and 3. The estimated pressures range from 70 to 270MPa in stage 1, through 30–150MPa in stage 2, to 30–85MPa in stage 3, corresponding to a depth of no less than 3km. In other words, the ore-forming fluids are characterized by high temperature, high salinity, high fO2 and high CO2 content; and fluid-boiling resulted in CO2 release, fO2 decrease and ore mineral precipitation. We suggest that the CO2-rich fluid is a distinctive feature of porphyry systems developed in continental collision setting, in transitional compressional to extensional regime, contrasting to the CO2-poor NaCl–H2O fluids observed in volcanic arcs. [Copyright &y& Elsevier]

The Caixiashan giant carbonate-hosted Zn–Pb deposit (~ 131 Mt@ 3.95% Zn + Pb) formed by replacement of dolomitized marble, with stratiform massive and breccia bodies is located near the base of the Proterozoic Kawabulake Group limestone and marble. It is one of the largest carbonated-hosted massive sulfides Zn–Pb ore deposits in Northwest China to have been discovered in recent years. Abundant pyrite occurs in dolomitized marble, along fractures in dolomitized clasts in the host rocks and filling cracks in the host rock. Locally, colloform or framboidal pyrites are observed in the early period and sometimes replaced by the later sphalerite. The sulfide assemblage of the main ore stage is characterized by massive or disseminated sphalerite and galena, with less pyrite than the earlier stage, and minor pyrrhotite. Galena occurs as small veins cutting the early-formed sphalerite. Dolomite and calcite are the main gangue minerals that co-precipitated with these sulfides. Tremolite and quartz alteration commonly overprints the orebodies. According to the crosscutting relationships and the different mineral associations within the host rocks and ore bodies, three stages are recognized at Caixiashan, i.e., syn-sedimentary pyrite (stage I), pyrite alteration, sphalerite–carbonate and galena–pyrite–carbonate (stage II-1, stage II-2 and stage II-3, respectively) and magmatic/metamorphic reworking (stage III). Calcite and quartz crystals are important host minerals among the three hypogene stages (stages I–III, although quartz mainly occurred in stage III). Stage I contains only aqueous inclusions (W-type), which were homogenized from 110 to 236 °C (main range of 138–198 °C and average at 168 °C; main range = average ± σ) and the salinities are from 0.5 to 16.5 (main range of 5.1–15.1 with average of 10.1) wt.% NaCl eqv. In the pyrite alteration of stage II-1 the W-type fluid inclusions homogenized from 175 to 260 °C (main range of 210–260 with average of 235) and the salinities range from 8.5 to 22.4 (main range of 16.7–20.1 with average of 18.4) wt.% NaCl eqv. In the main Zn–Pb mineralization stage (stage II-2–3), four types of fluid inclusions were identified an aqueous phase (W-type), a pure carbon phase (PC-type), a carbon phase containing (C-type) and mineral bearing inclusions (S-type). The W-type fluid inclusions of stage II-2–3 homogenized at 210 to 370 °C (main range of 253–323 and average at 270) and the salinities range from 5.9 to 23.1 (main range of 13.3–20.3 with average at 16.8) wt.% NaCl eqv.; C-type homogenized at 237 °C to 371 °C and the salinities range from 6.4–19.7 wt.% NaCl eqv.; S-type fluid inclusions homogenized at 211 to 350 °C and daughter minerals melted between 340 and 374 °C during heating, indicating a salinity range of 42 to 44 wt.% NaCl eqv. PC-type fluid inclusions with homogenization temperatures of CO 2 phase show large variation from 7.4 °C to 21.2 °C. Laser Raman analyses show that CH 4 , CO 2 and SO 4 2 − coexist in the main mineralization stage fluids. The magmatic/metamorphic reworking stage only contains W-type fluid inclusions which yield homogenized between 220 and 360 °C (main range of 251–325 and average at 288), with salinities ranging from 1.7 to 23.0 (main range of 14.3–20.0 and average at 18.8) wt.% NaCl eqv. The textural features, mineral assemblages and fluid geochemistry suggest that the Zn–Pb ores were formed through hydrothermal convection of hot marine waters along the faults and fractures resulting in metal (Zn, Pb and Fe) enriched stratiform orebodies. Subsequent rapid precipitation of sulfides was triggered by sulfate (SO 4 2 − ) thermal reduction with the CH 4 preserved in sedimentary rocks and early stage I pyrite bodies. This process occurred at moderate temperatures ( ca . 270 °C). Higher-temperature magmatic hydrothermal alteration overprinted the orebodies, but only provided a minor contribution to the mineralization. [ABSTRACT FROM AUTHOR]