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[Display omitted] • The tourmalines in Longmenshan are divided into two types, compositionally belongs to alkali group and schorl-dravite solid solution series. • The δ11B of the Tur-I tourmalines indicate the fluids that are responsible for the formation of tourmalines were derived mostly from the granitic magmas with little exotic oxide fluids involved. • The large range of B isotope variation indicates that the Tur-II tourmaline are more obviously affected by fluid activity. Tourmaline is a common mineral in rocks. It can record geological information during its formation and is a geochemical tracer. Its in-situ element and boron isotope tests provide a broader application perspective. Therefore, the chemical and boron isotope characteristics of tourmaline can be used to trace the mineralization of pegmatite-type rare metals. West Kunlun is an important Li-Be metallogenic belt, and many important Li-Be deposits have been developed. Longmenshan is one of the recently discovered pegmatite-type Li-Be deposits in the Dahongliutan area. There are barren and spodumene-bearing pegmatites that all contain tourmaline in Longmenshan. According to their occurrence, crystal form, and chemical composition, the tourmalines in Longmenshan are divided into two types: Tur-I tourmaline in the barren pegmatite close to the granite and Tur-II tourmaline from the spodumene-bearing pegmatite. Compositionally belongs to the alkali group and schorl-dravite solid solution series, with Tur-I being mainly schorl and Tur-II being schorl-dravite. Tur-I tourmalines are rich in Li, Sn, V, Cr, Zn, and Mn, while Tur-II tourmalines are rich in Be, Sr, and Sc. The δ11B of the Tur-I tourmalines hosted in the barren pegmatite and Tur-II from the spodumene-bearing pegmatite ranges from −8.38‰ to −6.81‰ and from −10.00‰ to −6.41‰, respectively. These characteristics indicate that the formation fluid of tourmaline in Longmenshan is mainly derived from magma, and other fluids are rarely involved. The large range of B isotope variation indicates that the Tur-II tourmalines are more obviously affected by fluid activity. [ABSTRACT FROM AUTHOR]

The newly discovered giant Dahutang W–Cu–Mo deposit in the central part of the Jiangnan Orogen hosts an estimated resource of 1.1 million tons (Mt) of WO 3 , plus a proven resource of 0.65 Mt Cu and 0.08 Mt Mo. The Dahutang deposit is temporally and spatially associated with the Late Mesozoic S-type granites emplaced into the Neoproterozoic Jiuling granodiorite batholith and the Shuangqiaoshan Group. Based on petrographic observations, eight hydrothermal alteration/mineralization stages have been recognized, comprising pegmatitic (Stage I), potassic alteration (Stage II), albite alteration (Stage III), greisenization and main mineralization (Stage IV), polymetallic sulfide mineralization (Stage V), late scheelite mineralization (Stage VI), carbonate alteration (Stage VII) and supergene alteration (Stage VIII). Stage IV can be further divided into the early greisenization (Stage IV-A), the main wolframite mineralization (Stage IV-B) and the main scheelite mineralization (Stage IV-C). Fluid inclusion and H–O isotope analyses on nine Stage IV to VII ore/gangue minerals (wolframite, cassiterite, scheelite, sphalerite, fluorapatite, fluorite, quartz, calcite and chlorite) suggest the presence of an early W and a late Cu–Mo ore-forming fluid system. The early ore-forming fluids belong to a medium to high temperature (200°–420 °C), low salinity H 2 O–NaCl–CaCl 2 system. This primary magmatic-hydrothermal fluid (δ 18 O fluid  = 5.4 to 8.8‰ and δD = −102 to −75‰) was likely exsolved from the Late Jurassic granites at Dahutang. Wolframite and scheelite coexist closely with fluorapatite and fluorite, respectively, indicating that the volatile-rich fluids at Dahutang were also rich in tungsten, fluorine and phosphorous. Tungsten was likely transported as tungstate species (e.g., WO 4 2− and HWO 4 − ), oxygen fluorine complexes (e.g., [WO 2 F 4 ] 2− , [WO 3 F 2 ] 2− ) and phosphorous heteropolytungstate (e.g., [P(W 12 O 40 )] 3− ) in the fluids. Fluorapatite and wolframite may have precipitated first when the temperature dropped from 400° to 320 °C (along with pH increase) at an estimated depth of 7.8 km. This was likely followed by the extensive scheelite mineralization (with fluorite precipitation) that formed huge disseminated/veinlet-type W orebodies when the temperature further dropped to 200 °C (along with pH increase). After the W mineralization, extensive Cu–Mo polymetallic mineralization and the associated sericite-chlorite alterations may have formed by the granite porphyry and/or muscovite granite emplacement. The late ore-forming fluids belong to a medium to high temperature (200°–360 °C), low salinity H 2 O–NaCl–CaCl 2 system. Molybdenum was likely transported mainly as Mo complexes (e.g., H 2 MoO 4 /MoO 4 2− ), and copper as Cu–Cl complexes. Molybdenite and chalcopyrite may have begun to precipitate when the fluids ascended and the temperature dropped to 330 °C. Meteoric water incursion may have then occurred (δ 18 O fluid  = 1.9–6.9‰ and δD = −99 to −68‰) and further cooled the fluid system to 250 °C, forming large Cu–Mo orebodies. [ABSTRACT FROM AUTHOR]

This study first described three-dimension images of a fluid inclusion hosted within sphalerite based on transmission nano X-ray tomography. It shows multiple shapes of the fluid inclusion viewed from different angles. This fluid inclusion contains both vapor and liquid phases, with irregular, asymmetry shape and concaved boundary. A reconstructed three-dimension animation viewer makes the shapes clearly. This study offers a technique to penetrate inside the fluid inclusion and calculate the volume of the single fluid inclusion based on the 3D images and animation, which can be applied for the future single fluid inclusion compositional studies. [ABSTRACT FROM AUTHOR]

The Shagou deposit, located in the eastern Qinling orogenic belt, central China and hosted by the Taihua Supergroup, is a large-sized Ag–Pb–Zn deposit and has proven reserves of 1.54million tons of ore with grades of 767g/t Ag, 13.24% Pb and 4.31% Zn. The ore-forming fluids have been previously interpreted as products of direct exsolution of a crystallizing magma or sudden decompression of the fluid exsolved from magma, defining the Shagou deposit as an intrusion-related system. In this study, the Shagou deposit has been identified as an orogenic type mineralization system. The hydrothermal ore-forming process can be divided into the early quartz–pyrite, middle quartz–polymetallic sulfides and late quartz–carbonate stages. Four types of fluid inclusions in quartz can be distinguished between PC, C, W and PW types. The early and middle stage quartz contains the PC, C and W type fluid inclusions, while only W and PW type fluid inclusions can be observed in the late stage quartz. In the early stage, the W type fluid inclusions homogenized at 173–369°C (concentrating at 200–240°C), with salinities ranging from 5.4 to 8.3wt.% NaCl equiv. But in the middle stage, the C and W type fluid inclusions homogenized at 112–313°C (concentrating at 180–220°C), with salinities ranging from 0.7 to 13.6wt.% NaCl equiv. In the late stage, the W type fluid inclusions homogenized at 108–253°C (concentrating at 160–200°C), with salinities ranging from 2.1 to 8.1wt.% NaCl equiv. The fluids may have experienced a boiling process or fluid mixing in the middle stage. The estimated trapping pressures of fluid inclusions in the middle stage ranged from 33 to 211MPa, corresponding to a mineralization depth from 3.3 to 7.7km. For the early stage fluids, the calculated δ18OH2O and δDH2O values are 7.5–9.1‰, −96.2 to −110.5‰, respectively. For the middle stage fluids, these two values are 1.5–5.3‰, −75.6 to −110.7‰ but change to 1.0‰ and −87‰ for the late stage, suggesting an evolution from metamorphic to meteoric in origin. In general, the Shagou Ag–Pb–Zn deposit is similar in many respects to typical orogenic type mineralization systems. [ABSTRACT FROM AUTHOR]

The Dashui porphyry granitoids in the western Qinling Orogen are spatially associated with the Dashui gold deposit, but their ages and tectonic setting have not been well defined yet in previous studies. This paper reports the results and understandings obtained from our original study in geochronology and isotope and element geochemistry. SHRIMP zircon U-Pb dating yielded ages of 213.7 ± 2.7 Ma for granitic stock and 215.1 ± 2.5 and 210.2 ± 1.6 Ma for granitic dikes. The granitoids are characterized by high LREE but low HREE and HFSE. They have (87Sr/86Sr) i ratios of 0.706 to 0.709 and εNd(t) values of −5.3 to −7.6. The majority of zircons in the Dashui granitoids have εHf(t) values ranging from −6.2 to 6.7 and TDM2(Hf) ages from 743 to 1464 Ma. The isotope signatures, together with La/Y and Mg# values, show that the magmas are mainly sourced from partial melting of a subducted slab, and possibly assimilated immature sediments during upward migration. Thus, the Dashui granitoids most likely formed in a volcanic arc where supra-subduction zone melts assimilated lower crustal material no later than 215 Ma. Copyright © 2014 John Wiley & Sons, Ltd. [ABSTRACT FROM AUTHOR]

[Display omitted] • Zircon U-Pb ages record two phases of granitic magmatism of 159 and 145 Ma. • Molybdenum and W are enriched in porphyry by prolonged fractionation and high f O2. • Scheelite petrography and compositions reflect mechanisms of Mo-W mineralization. • Porphyry-skarn Mo-W systems may be controlled by magmatic sources and wall rocks. Eastern Qinling Orogen is the largest Mo province in the world, hosting nine giant Mo deposits. Four giant Mo deposits contain economic W mineralization, while the mechanism of W mineralization remains unclear. The Yechangping deposit is a representative porphyry-skarn Mo-W deposit, with four paragenetic stages of prograde skarn, retrograde skarn, polymetallic sulfides and carbonate stage. Magmatism at Yechangping includes early barren monzogranite porphyry at 159.0 ± 1.5 Ma and late ore-related granite porphyry at ca. 145 Ma, and the latter porphyry shows a higher magmatic fractionation than the early barren monzogranite porphyry. Both barren and ore-related porphyries have similar high magma oxidation states, which may efficiently extract Mo during partial melting and hinder subsequent molybdenite crystallization until the porphyry-skarn Mo mineralization. Three types of scheelites are distinguished by their texture, paragenetic relationship and geochemistry, including Sch-1a in the retrograde skarn stage, and Sch-1b and Sch-2 in the polymetallic sulfides stage. Scheelite displays decreasing MoO 3 contents from 7.01–51.59 % in Sch-1a, through 3.15–17.51 % in Sch-1b, to 0–1.51 % in Sch-2. The decreasing MoO 3 contents in scheelite are attributed to the transformation of dominant Mo-bearing phases, i.e., from retrograde skarn stage powellite to polymetallic sulfides stage molybdenite. We suggest that the Mo-W mineralization is triggered by the decreasing oxygen fugacity, p H, and temperature, supported by thermodynamic modeling. In addition, the precipitation of fluorite and destabilization of fluorine complexes may have also promoted the Mo-W mineralization. Zircon Hf isotopes yielded ε Hf (t) values of −14.9 to −7.5 and T DM2 ages of 1671–2147 Ma, indicating that Yechangping porphyries were primarily sourced from the ancient basement of the Huaxiong Block, with additional contribution from the North Qinling Accretionary Belt. Skarn W mineralization in the southern part of Huaxiong Block may be controlled by both magmatic fertility and carbonate wall-rocks. [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]

[Display omitted] • Five ore-forming stages are recognized in the Yechangping porphyry-type orebodies. • Fluid characteristics suggest that Yechangping is a Dabie-type porphyry Mo deposit. • The process of fluid immiscibility, boiling, and mixing cause the mineralization. • Magmatic-hydrothermal system of Yechangping deposit extends to depths of 10 km. Dabie-type porphyry Mo deposits have recently emerged as a distinct subtype of porphyry Mo deposits, but questions remain about the magmatic-hydrothermal fluid evolution in the formation of this type of deposit. Here, well-developed fluid inclusions in quartz phenocrysts, unidirectional solidification textures (UST), and quartz veins in the Yechangping porphyry Mo-W deposit, Qinling Orogen, completely record the magmatic-hydrothermal mineralization process. The characteristics and evolution of the ore-forming fluid in this deposit are investigated through petrography, microthermometry, and laser Raman spectroscopy analysis of fluid inclusions at different stages in order to improve our understanding of the fluid evolution in the genesis of Dabie-type porphyry Mo deposit. The mineralization process in the porphyry-type orebody can be divided into three periods and five stages: (1) magmatic period, including quartz phenocrysts (stage 1); (2) magmatic-hydrothermal transition period, including UST (stage 2); (3) hydrothermal period, including quartz ± K-feldspar veins (stage 3), quartz-molybdenite veins (stage 4), and calcite ± quartz veins (stage 5), where stage 4 is the main ore-forming stage. The fluid inclusions in quartz and calcite can be recognized as pure CO 2 (PC type), CO 2 -H 2 O (C type), daughter minerals-bearing (S type), and H 2 O (WV type and WL type) inclusions. Ore-forming fluid is initially high temperature, high salinity, and CO 2 -rich, belonging to the H 2 O-CO 2 -NaCl (±KCl) system suggested by the fluid inclusions identified in UST. The estimated lithostatic pressures of stage 1 range from 284–362 MPa, corresponding to depths of 10.3 to 13.2 km, which are consistent with the formation depth of the underlying magma chamber. The presence of UST in stage 2 indicates that the magma was saturated with fluid. Due to the fluctuating pressure (123–260 MPa) in UST of stage 2, fluid immiscibility happened soon after the fluid exsolution and is inferred to occur between the CO 2 -rich and aqueous phases. Then, the fluid boiling and mixing occurred in stages 3 and 4, respectively. The estimated pressures of stage 4, which represent the main mineralization stage, range from 45–175 MPa, corresponding to depths of 4.6–6.4 km. The immiscibility of CO 2, along with the fluid mixing-induced cooling and dilution, caused an increase in p H and a decrease in oxygen fugacity, which serves as a crucial mechanism for Mo mineralization at the Yechangping deposit. Stage 5 is characterized by low temperature (185–309 °C) and low salinity (2.9–8.7 wt% NaCl equiv.). The primary high temperature, high salinity, CO 2 -rich fluids, and relatively deep ore-forming depth suggest that the Yechangping deposit is a typical example of a Dabie-type porphyry deposit. The characteristics of fluids and the variation in estimated depth at each stage record the evolutionary process of a magmatic-hydrothermal system extending to depths of nearly 10 km in the Yechangping deposit. [ABSTRACT FROM AUTHOR]

[Display omitted] • The hydrothermal titanite associated with Au mineralization was formed at 130.8 ± 0.63 Ma. • The early Cretaceous Au mineralization overprinted the Triassic and late Jurassic Mo-Pb mineralization in Huangshui'an. • The gold precipitation mechanisms are sulfidation, collection-redissolution by LMCE melt, and changes in f Te 2 and f S 2. Huangshui'an deposit, situated in the Xiong'ershan area of Qinling orogenic belt (QOB) in China, is a globally rare carbonatite-type molybdenum polymetallic deposit that contains economic Mo, Au, Pb, and REE mineralization. The molybdenite Re-Os ages (Ca. 213.5–209.2 Ma) indicates that Huangshui'an Mo mineralization formed at Late Triassic. However, it is still unclear whether the Au mineralization is related to carbonatite dykes, and the formation age and genesis mechanism of Au mineralization remain poorly understood at Huangshui'an. This paper presents a comprehensive investigation of the Au mineralization events at the Huangshui'an deposit, including geology, mineralogy, and geochronology. The aim is to provide insights into its formation and mineralization processes and offer a broader understanding of regional Au metallogeny. Based on petrographic investigations, four stages are identified in the Au mineralization as follows: (I) quartz-K-feldspar stage; (II) quartz-pyrite-gold stage, including (IIA) pyrite-native gold sub-stage and (IIB) gold-tellurite-bismuthide sub-stage; (III) quartz-pyrite-polymetallic sulphide-oxide stage; and (IV) calcite-quartz-chlorite stage. The LA-ICP-MS titanite U-Pb dating yields a weighted mean age of 130.8 ± 0.63 Ma which determined that the Au mineralization at Huangshui'an was in the Early Cretaceous and was an independent mineralization event, which may be related to the lithosphere's destructive effect on the North China Craton (NCC). Combined with mineralography by automatic quantitative mineral analysis and testing system (TIMA), we consider that tellurium-bismuth minerals are closely associated with Au mineralization. The sulfur and tellurium fugacity of the ore-forming fluids in each stage were calculated using metal sulfide-oxides and tellurium-bismuth minerals. It was concluded that the precipitation of Au in the Huangshui'an deposit was mainly due to the combined effects of sulfidation, gold collection-redissolution by the low-melting point chalcophile elements (LMCE) melts, and the variation of sulfur fugacity and tellurium fugacity. [ABSTRACT FROM AUTHOR]

[Display omitted] • Mo isotopes variation in both the two Mo deposits may be controlled by Rayleigh and equilibrium fractionation. • The Taihua Soupergroup and the Xiong'er Group would be the main contributor of Mo metal for the Paleoproterozoic Mo mineralization. • The mantle with light isotopically Mo involved into the Mo Paleoproterozoic mineralization in Qinling orogenic belt. Longmendian and the Zhaiwa are the two oldest Mo deposits in the Qinling orogenic belt, China, which is one of the most important Mo provinces in the world with numerous and diverse types of Mo deposits that experienced multistaged mineralization. Here we investigated Mo isotope compositions in molybdenite and rocks from the Longmendian and the Zhaiwa Paleoproterozoic Mo deposits to link Mo isotopes to the sources of Mo metal. The significant Mo isotope variation in the Longmendian and the Zhaiwa Mo deposits (δ98Mo = −0.51‰ to + 1.01‰ and −0.37‰ to +0.53‰, respectively, relative to NIST-3134) may be controlled by Rayleigh and equilibrium fractionation. The different distributions of Mo isotope compositions of molybdenite in the two deposits may be caused by the physiochemical differences in ore-forming systems. The high Mo content of the Taihua Supergroup and the Xiong'er Group, combined mean values of Mo isotopes between molybdenite and whole rocks suggested that the two stratigraphic units would be the main contributor of Mo for the Paleoproterozoic Mo mineralization that mixed with small proportions of isotopically lower values of the mantle. [ABSTRACT FROM AUTHOR]

The Waifangshan Mo-quartz vein cluster occurs at the northernmost margin of the Qinling Orogen. The orebodies occur as quartz veins and are controlled by low-angle faults. We identify three hydrothermal stages, characterized by veinlets of quartz–pyrite, quartz–molybdenite–pyrite–chalcopyrite–galena–sphalerite, and quartz–carbonate assemblages, respectively. The early-stage quartz veins were structurally-deformed, brecciated, and filled by non-deformed middle- or late-stage veinlets, suggesting that the mineralization is associated with a tectonic transition from compression to extension. Five molybdenite separates from the Zhifang Mo deposit yield individual Re–Os ages from 241.2 ± 1.6 to 247.4 ± 2.5 Ma, with a weighted mean age of 243.8 ± 2.8 Ma. Individual Re–Os isotope ages of four molybdenite samples from the Badaogou Mo deposit range from 238.9 ± 2.1 to 255.8 ± 2.2 Ma, with a weighted mean age of 246 ± 10 Ma. Four analyses of molybdenite separates from the Xiangchungou Mo deposit yield individual Re–Os isotope ages of 243.8 ± 8.8 to 247.7 ± 4.4 Ma, with a weighted mean age of 246.0 ± 1.1 Ma. All of these data yield a weighted mean age of 241.9 ± 1.9 Ma, coeval with the accretionary orogeny. We thus conclude that the Waifangshan Mo-quartz veins formed during a transition from continental arc to back-arc setting. The Waifangshan Mo-quartz veins share similar geological, geochemical and geochronological features with the orogenic-type systems. We propose that the Waifangshan Mo-quartz veins are an orogenic-type Mo mineralization, and possibly represent the deepest member in the crustal continuum model of the orogenic-type mineral systems. The molybdenite samples from the Mo-quartz veins in the Waifangshan area have low Re contents (1.457 to 39.16 ppm), suggesting a continental crust-dominated source. [ABSTRACT FROM AUTHOR]

The Tumen Mo–F deposit is located on the southern margin of the North China Craton in central China. The deposit represents a fluorite-vein system hosted by carbonate rocks in the Neoproterozoic Luanchuan Group. Previous studies identify four hydrothermal stages at the deposit characterized by: Stage 1 veins of white fluorite, Stage 2 purple fluorite–molybdenite–pyrite (–galena), Stage 3 calcite–galena–pyrite–sphalerite (–chalcopyrite), and Stage 4 carbonate assemblages. The δ 34 S values for sulfides from the Tumen deposit range between −7.1 and 5.0‰, with a bimodal distribution. The Stage 2 sulfides have δ 34 S values of −2.7 to 5.0‰ that are similar to that of granitic rocks, but different from andesite in the Xiong’er Group, amphibolitic gneiss in the Taihua Supergroup and the carbonaceous shale and chert in the Luanchuan Group. The near-zero δ 34 S values indicate a possible magmatic source for the Stage 2 fluids. However, the δ 34 S values for the Stage 3 sulfides have negative mean and a restricted range from −7.1 to −4.6‰, which is different from that of the Xiong’er Group and Taihua Supergroup. The 34 S-depleted fluid for the Stage 3 sulfides was inherited from the host rocks in the Luanchuan Group with low δ 34 S values of −12.4 to 7.2‰. New Sr–Nd–Pb isotope data obtained from fluorite at Tumen indicate that the fluorite has higher Pb-isotope ratios, higher ɛ Nd(t) and lower I Sr (t) values than the host rocks. The results suggests that the ore-forming fluids had ɛ Nd(t) > −4.8, I Sr (t) < 0.7068, ( 206 Pb/ 204 Pb) i > 17.998, ( 207 Pb/ 204 Pb) i < 15.576 and ( 208 Pb/ 204 Pb) i < 38.201, which overlap the values of ( ɛ Nd(t) = −3.8 to −1.3, I Sr (t) = 0.7006–0.7061 for Neoproterozoic syenite in Qinling Orogen. This suggests that the deposit is related to a magmatic hydrothermal vein system associated with Neoproterozoic syenitic magmatism. [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]