Geology,fluid inclusion geochemistry,and 40Ar/39Ar geochronology of the Wulasigou Cu deposit,and their implications for ore genesis,Altay, Xinjiang,China

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 0.9–6.5 wt.% 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 0.9–2.9 wt.% 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 2.7–10.2 wt.% NaCl equiv for the W-, M- and C-types, and 34.7–38.2 wt.% 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 1.55–3.55 kbar, suggesting an alternating lithostatic-hydrostatic fluid-system, controlled by fault-valve activity at a depth of 13–15.5 km.Muscovite separates from the middle-stage polymetallic-quartz veinlets yield a well-defined ⁴⁰Ar/³⁹Ar isotopic plateau age of 219.41 ± 2.10 Ma, and an ³⁹Ar/³⁶Ar - ⁴⁰Ar/³⁶Ar isochron age of 219.73 ± 2.17 Ma. This age postdates the final Paleo-Asia Ocean closure (at ca. 250 Ma) by about 30 Ma, 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.     

Geology and fluid evolution of the Wangfeng orogenic-type gold deposit,Western Tian Shan,China

The Wangfeng gold deposit is located in Western Tian Shan and the central section of the Central Asian Orogenic Belt (CAOB). The deposit is mainly hosted in Precambrian metamorphic rocks and Caledonian granites and is structurally controlled by the Shenglidaban ductile shear zone. The gold orebodies consist of gold-bearing quartz veins and altered mylonite. The mineralization can be divided into three stages: quartz–pyrite veins in the early stage, sulfide–quartz veins in the middle stage, and quartz–carbonate veins or veinlets in the late stage. Ore minerals and native gold mainly formed in the middle stage. Four types of fluid inclusions were identified based on petrography and laser Raman spectroscopy: CO₂–H₂O inclusions (C-type), pure CO₂ inclusions (PC-type), NaCl–H₂O inclusions (W-type), and daughter mineral-bearing inclusions (S-type). The early-stage quartz contains only primary CO₂–H₂O fluid inclusions with salinities of 1.62 to 8.03 wt.% NaCl equivalent, bulk densities of 0.73 to 0.89 g/cm³, and homogenization temperatures of 256 °C–390 °C. Vapor bubbles are composed of CO₂. The middle-stage quartz contains all four types of fluid inclusions, of which the CO₂–H₂O and NaCl–H₂O types yield homogenization temperatures of 210 °C–340 °C and 230 °C–300 °C, respectively. The CO₂–H₂O fluid inclusions have salinities of 0.83 to 9.59 wt.% NaCl equivalent and bulk densities of 0.77 to 0.95 g/cm³, with vapor bubbles composed of CO₂, CH₄, and N₂. Fluid inclusions in the late-stage quartz are NaCl–H₂O solution with low salinities (0.35–3.87 wt.% NaCl equivalent) and low homogenization temperatures (122 °C–214 °C). The coexistence of inclusions of these four types in middle-stage quartz suggests that fluid boiling occurred in the middle-stage mineralization. Trapping pressures estimated from CO₂–H₂O inclusions are 110–300 MPa and 90–250 MPa for the early and middle stages, respectively, suggesting that gold mineralization mainly occurred at depths of about 10 km. In general, the Wangfeng gold deposit originated from a metamorphic fluid system characterized by low salinity, low density, and enrichment of CO₂. Depressurized fluid boiling caused gold precipitation. Given the regional geology, ore geology, fluid-inclusion features, and ore-forming age, the Wangfeng gold deposit can be classified as a hypozonal orogenic gold deposit.     

Timing and mechanism of gold mineralization at the Wang'ershan gold deposit,Jiaodong Peninsula,eastern China

The Wang'ershan gold deposit, located in the southern Jiaojia goldfield, is currently the largest gold deposit hosted within the subsidiary faults in Jiaodong Peninsula, with a gold reserve of > 60 t gold at a grade of 4.07 g/t Au. It is hosted in the Late Jurassic Linglong biotite granites and controlled by the second-order, N- to NNE-trending Wang'ershan Fault (and its subsidiary faults) which is broadly parallel to the first-order Jiaojia Fault in the goldfield. Gold mineralization occurs as both disseminated- and stockwork-style and quartz–sulfide vein-style ores, mainly within altered cataclasites and breccias, and sericite–quartz and potassic alteration zones, respectively. Mineralization stages can be divided into (1) the pyrite–quartz–sericite stage, (2) the quartz–pyrite stage, (3) the quartz–sulfide stage, and (4) the quartz–carbonate stage.Two sericite samples associated with the main ore-stage pyrites from pyritic phyllic ores of the deposit with weighted mean plateau ⁴⁰Ar/³⁹Ar age of 120.7 ± 0.6 Ma and 119.2 ± 0.5 Ma, respectively, were selected for ⁴⁰Ar/³⁹Ar geochronology. On the basis of petrography and microthermometry, three types of primary fluid inclusions related to the ore forming event were identified: type 1 H₂O–CO₂–NaCl, type 2 aqueous, and type 3 CO₂ fluid inclusions (in decreasing abundance). Stage 1 quartz contains all three primary fluid inclusions, while stages 2 and 3 quartz contain both type 1 and 2 inclusions, and stage 4 quartz contains only type 2 inclusions. The contemporaneous trapping, similar salinities and total homogenization temperature ranges, and different homogenization phases of type 1 and type 2 inclusions indicate that fluid immiscibility did take place in stages 1, 2 and 3 ores, with P–T conditions of 190 to 85 MPa and 334 to 300 °C for stage 1 and 200 to 40 MPa and 288 to 230 °C for stages 2 and 3. Combined with the H–O–C–S–Pb isotopic compositions, ore-forming fluids may have a metamorphic-dominant mixed source, which could be associated with the dehydration and decarbonisation of a subducting paleo-Pacific plate and characterized by medium–high temperature (285–350 °C), CO₂-bearing (~ 8 mol%) with minor CH₄ (1–4% in carbonic phase), and low salinity (3.38–8.45 eq. wt.% NaCl). During mineralization, the fluid finally evolved into a medium–low temperature NaCl–H₂O system. Au(HS)₂⁻ was the most probable gold-transporting complex at Wang'ershan, due to the low temperature (157–350 °C) and near-neutral to weakly acidic ore fluids. The reaction between gold-bearing fluids and iron-bearing wall-rocks, and fluid-immiscibility processes caused via fluid–pressure cycling during seismic movement along fault zones that host lode-gold orebodies, which led to breakdown of Au(HS)₂⁻, are interpreted as the two main precipitation mechanisms of gold deposition.In general, the Wang'ershan deposit and other deposits in the Jiaojia camp have concordant structural system and wall-rock alteration assemblages, nature of orebodies and gold occurrence conditions, as well as the similar geochronology, ore-forming fluids system and stable isotope compositions. Thus gold mineralization in the Jiaojia goldfield was a large-scale unified event, with consistent timing, origin, process and mechanism.     

Geology,geochemistry and age of the Hukeng tungsten deposit,Southern China

The Hukeng tungsten deposit, located in the Wugongshan area in central part of Jiangxi province, South China, is a large-scale quartz-vein wolframite deposit. It is hosted in the Hukeng granitic intrusion. Based on the mineral assemblage and crosscutting relationship of the veins, three mineralization stages are identified, including: (1) quartz–wolframite stage, (2) quartz–fluorite–wolframite stage, and (3) quartz–pyrite–sphalerite–wolframite stage.The homogenization temperatures of fluid inclusions in vein quartz vary from 220 to 320 °C, and the salinities are from 0 to 10 wt.% NaCl equiv.; corresponding densities range from 0.7 to 1 g/cm³. These features indicated that the ore-forming fluids in the Hukeng tungsten deposit have medium temperature, low density and low salinity.The δ¹⁸OSMOW values of quartz range from 10.8‰ to 14.4‰, with corresponding δ¹⁸O_fluid values of 3.7‰ to 7.7‰, and δD values of fluid inclusions of between ? 70‰ and ? 55‰. The combined isotopic data indicate that the ore-forming fluids of the Hukeng tungsten deposit were mainly derived from magmatic water, with some minor input from meteoric water.We have carried out molybdenite Re–Os and muscovite ⁴⁰Ar/³⁹Ar dating to constrain the timing of mineralization. Re–Os dating of six molybdenite samples yielded model ages ranging from 149.1 ± 2.0 to 150.7 ± 3.7 Ma, with an average of 150.0 Ma. The Re–Os analyses give a well-defined ¹⁸⁷Re/¹⁸⁷Os isochron with an age of 150.2 ± 2.2 Ma (MSWD = 0.60). Hydrothermal muscovite yields a plateau ⁴⁰Ar/³⁹Ar age of 147.2 ± 1.4 Ma. ⁴⁰Ar/³⁹Ar age is in good agreement with the Re–Os age. These ages show that the timing of tungsten mineralization occurred at about 150 Ma. Our new data, when combined with published geochronological results from the other major deposits in this region, suggest that widespread W mineralization occurred in the Late Jurassic throughout South China.     

Fluid inclusion geochemistry and Ar–Ar geochronology of the Cenozoic Bangbu orogenic gold deposit,southern Tibet,China

Located along the southern part of the Yarlung Zangbo suture zone in southern Tibet, Bangbu is one of the largest gold deposits in Tibet. Auriferous sulfide-bearing quartz veins are controlled by second- or third-order brittle fractures associated with the regional Qusong–Cuogu–Zhemulang brittle-ductile shear zone. Fluid inclusion studies show that the auriferous quartz contains aqueous inclusions, two-phase and three-phase CO₂-bearing inclusions, and pure gaseous hydrocarbon inclusions. The CO₂-bearing inclusions have salinities of 2.2–9.5% NaCl_eq, and homogenization temperatures (Th) of 167–336 °C. The δD, δ¹⁸O, and δ¹³C compositions of the Bangbu ore-forming fluids are − 105.5 to − 44.4‰, 4.7 to 9.0‰ and − 5.1 to − 2.2‰, respectively, indicating that the ore-forming fluid is mainly of metamorphic origin, with also a mantle-derived contribution. The ³He/⁴He ratio of the ore-forming fluids is 0.174 to 1.010 R_a, and ⁴⁰Ar/³⁶Ar ranges from 311.9 to 1724.9. Calculations indicate that the percentage of mantle-derived He in fluid inclusions from Bangbu is 2.7–16.7%. These geochemical features are similar to those of most orogenic gold deposits. Dating by ⁴⁰Ar/³⁹Ar of hydrothermal sericite collected from auriferous quartz veins at Bangbu yielded a plateau age of 44.8 ± 1.0 Ma, with normal and inverse isochronal ages of 43.6 ± 3.2 Ma and 44 ± 3 Ma, respectively. This indicates that the gold mineralization was contemporaneous with the main collisional stage between India and Eurasia along the Yarlung Zangbo suture, which resulted in the development of near-vertical lithospheric shear zones. A deep metamorphic fluid was channeled upward along the shear zone, mixing with a mantle fluid. The mixed fluids migrated into the brittle structures along the shear zone and precipitated gold, sulfides, and quartz because of declining temperature and pressure or fluid immiscibility. The Bangbu is a large-scale Cenozoic syn-collisional orogenic gold deposit     

Evidence of fluid inclusions for two stages of fluid boiling in the formation of the giant Shapinggou porphyry Mo deposit,Dabie Orogen,Central China

The Shapinggou porphyry Mo deposit, one of the largest Mo deposits in Asia, is located in the Dabie Orogen, Central China. Hydrothermal alteration and mineralization at Shapinggou can be divided into four stages, i.e., stage 1 ore-barren quartz veins with intense silicification, followed by stage 2 quartz-molybdenite veins associated with potassic alteration, stage 3 quartz-polymetallic sulfide veins related to phyllic alteration, and stage 4 ore-barren quartz ± calcite ± pyrite veins with weak propylitization. Hydrothermal quartz mainly contains three types of fluid inclusions, namely, two-phase liquid-rich (type I), two- or three-phase gas-rich CO₂-bearing (type II) and halite-bearing (type III) inclusions. The last two types of fluid inclusions are absent in stages 1 and 4. Type I inclusions in the silicic zone (stage 1) display homogenization temperatures of 340 to 550 °C, with salinities of 7.9–16.9 wt.% NaCl equivalent. Type II and coexisting type III inclusions in the potassic zone (stage 2), which hosts the main Mo orebodies, have homogenization temperatures of 240–440 °C and 240–450 °C, with salinities of 34.1–50.9 and 0.1–7.4 wt.% NaCl equivalent, respectively. Type II and coexisting type III inclusions in the phyllic zone (stage 3) display homogenization temperatures of 250–345 °C and 220–315 °C, with salinities of 0.2–6.5 and 32.9–39.3 wt.% NaCl equivalent, respectively. Type I inclusions in the propylitization zone (stage 4) display homogenization temperatures of 170 to 330 °C, with salinities lower than 6.5 wt.% NaCl equivalent. The abundant CO₂-rich and coexisting halite-bearing fluid inclusion assemblages in the potassic and phyllic zones highlight the significance of intensive fluid boiling of a NaCl–CO₂–H₂O system in deep environments (up to 2.3 kbar) for giant porphyry Mo mineralization. Hydrogen and oxygen isotopic compositions indicate that ore-fluids were gradually evolved from magmatic to meteoric in origin. Sulfur and lead isotopes suggest that the ore-forming materials at Shapinggou are magmatic in origin. Re–Os dating of molybdenite gives a well-defined ¹⁸⁷Re/¹⁸⁷Os isochron with an age of 112.7 ± 1.8 Ma, suggesting a post-collisional setting.     

Geological,geochronological, and H–O isotopic constraints on the genesis of the Tongjing Cu–Au deposit in the Ningwu basin,east China

The Tongjing Cu–Au deposit is a medium-sized deposit within the Ningwu volcanic basin, east China, and is hosted by Cretaceous volcanic rocks of the Dawangshan and Niangniangshan Formations. The veined and lenticular Cu–Au orebodies are spatially and temporally related to the volcanic and subvolcanic rocks of the Niangniangshan Formation in the ore district. The wall-rock alteration is dominated by silicification, siderite alteration, carbonation, sericitization, chloritization, and kaolinization. On the basis of field evidence and petrographic observations, two stages of mineralization are recognized: (1) a siderite–quartz–sulfide stage (Stage 1) associated with the formation of chalcopyrite and pyrite in a quartz and siderite gangue; and (2) a quartz–bornite stage (Stage 2) cutting the Stage 1 phases. Stage 1 is the main mineralization stage. Quartz that formed in Stage 1 has δ¹⁸O_H2O values of − 4.3‰ to 3.5‰ with δD values of fluid inclusion waters of − 97.1‰ to − 49.9‰, indicating that the ore-forming fluids were derived from early magmatic fluids and may have experienced oxygen isotopic exchange with meteoric water during Stage 1 mineralization.LA–MC–ICP–MS zircon U–Pb dating of the mineralization-related nosean-bearing phonolite and nosean-bearing phonolitic brecciated tuff at Tongjing yields ages of 129.8 ± 0.5 Ma and 128.9 ± 1.1 Ma, respectively. These results are interpreted as the crystallization age of the volcanic rocks of the Niangniangshan Formation. A hydrothermal sericite sample associated with Cu–Au mineralization at Tongjing yields a plateau ⁴⁰Ar–³⁹Ar age of 131.3 ± 1.3 Ma. These results confirm a genetic link between the volcanism and associated Cu–Au mineralization. The Tongjing Cu–Au deposit in the Ningwu basin is genetically and possibly tectonically similar to alkaline intrusion-related gold deposits elsewhere in the world.     

Origin of fluids in the Hetaoping Pb–Zn deposit,Baoshan–Narong–Dongzhi block metallogenic belt,Yunnan Province,SW China

The Hetaoping skarn type Pb–Zn deposit is located in the Baoshan–Narong–Dongzhi block metallogenic belt (BND belt), a belt between the Tengchong terrane and the Lanping basin. The deposit is hosted by marble of the upper Cambrian Hetaoping Formation and there are no outcrops of plutonic rocks present. This deposit is one of two large Pb–Zn deposits recently discovered in the BND belt. The Hetaoping deposit is a high Mn skarn. Four types of fluid inclusions were recognized in quartz from the deposit: vapor-rich inclusions (Type I), liquid-rich inclusions (Type II), pure vapor inclusions (Type III), and pure fluid inclusions (Type IV). The coexistence of Type I and Type III inclusions in Stage I (pre-ore stage) and Stage II (main ore stage) shows evidence of fluid boiling. Quartz-hosted fluid inclusions (Stage I and Stage II) display high homogenization temperatures and salinities (134–315 °C; 3.7–18.6 wt% NaCl equivalent) but calcite-hosted fluid inclusions in Stage III (post-ore stage) record lower homogenization temperatures and salinities (85–214 °C; 0.5–5.4 wt% NaCl equivalent). These data suggest a possible mixing between primary magmatic water and meteoric water. Based on chromatography data, the fluid inclusions in quartz contain abundant CO₂ and O₂ and subordinate CO, CH₄ and C₂H₂ + C₂H₄, suggesting an oxidizing environment. Based on their Na/K and Cl/SO₄ ratios, fluids contained in fluid inclusions are similar to volcanic spring waters. The low Na/K ratios (0.40–1.34) of the ore-forming fluids may have resulted from interaction with a deep alkaline intermediate-acid intrusion. Hydrogen and oxygen isotope determinations on quartz from different ore stages show low δ¹⁸O and δD values relative to VSMOW (−4.3‰ to 2.3‰; −109‰ to −91‰), indicating that the ore-forming fluids were diluted by external fluid sources as the skarn system cooled. Overall, geological and geochemical interpretations suggest that the Hetaoping deposit is a distal manganese skarn Pb–Zn deposit related to concealed intrusions.     

40Ar/39Ar dating of the Jiehe gold deposit in the Jiaodong Peninsula,eastern North China Craton: Implications for regional gold metallogeny

The Jiehe gold deposit, containing a confirmed gold reserve of 34 tonnes (t), is a Jiaojia-type (disseminated/stockwork-style) gold deposit in Jiaodong Peninsula. Orebodies are hosted in the contact zone between the Jurassic Moshan biotite granite and the Cretaceous Shangzhuang porphyritic granodiorite, and are structurally controlled by the NNE- to NE-striking Wangershan-Hedong Fault. Sulphide minerals are composed predominantly of pyrite with lesser amounts of chalcopyrite, galena, and sphalerite. Hydrothermal alteration is strictly controlled by fracture zones, in which disseminated sulfides and native gold are spatially associated with pervasive sericitic alteration. Mineralogical, textural, and field relationships indicate four stages of alteration and mineralization, including pyrite-bearing milky and massive quartz (stage 1), light-gray granular quartz–pyrite (stage 2), quartz–polysulfide (stage 3) and quartz–carbonate (stage 4) stages. Economic gold is precipitated in stages 2 and 3.The Jiehe deposit was previously considered to form during the Eocene (46.5 ± 2.3 Ma), based on Rb-Sr dating of sericite. However, ⁴⁰Ar/³⁹Ar dating of sericite in this study yields well-defined, reproducible plateau ages between 118.8 ± 0.7 Ma and 120.7 ± 0.8 Ma. These ⁴⁰Ar/³⁹Ar ages are consistent with geochronological data from other gold deposits in the region, indicating that all gold deposits in Jiaodong formed in a short-term period around 120 Ma. The giant gold mineralization event has a tight relationship with the extensional tectonic regime, and is a shallow crustal metallogenic response of paleo-Pacific slab subduction and lithospheric destruction in the eastern NCC.     

Geology,geochronology and fluid characteristics of the Pingqiu gold deposit,Southeastern Guizhou Province,China

The junction of the southeastern Guizhou, the southwestern Hunan, and the northern Guangxi regions is located within the southwestern Jiangnan orogen and forms a NE-trending ∼250 km gold belt containing more than 100 gold deposits and occurrences. The Pingqiu gold deposit is one of the numerous lode gold deposits in the southeastern Guizhou district. Gold mineralization is hosted in Neoproterozoic lower greenschist facies metamorphic rocks and controlled by fold-related structures. Vein types present at Pingqiu include bedding-parallel and discordant types, with saddle-reefs and their down limb extensions dominating but with lesser discordant types. The major sulfide minerals are arsenopyrite and pyrite, with minor sphalerite, galena, chalcopyrite, and rare pyrrhotite, marcasite, and tetrahedrite. Much of the gold is μm- to mm-sized grains, and occurs as fracture-controlled isolated grains or filaments in quartz, galena, sphalerite, pyrite, and wallrock.Three types of fluid inclusions are distinguished in hydrothermal minerals. Type 1 aqueous inclusions have homogenization temperatures of 171–396 °C and salinities of 1.4–9.8 wt% NaCl equiv. Type 2 aqueous-carbonic inclusions yield final homogenization temperatures of 187–350 °C, with salinities of 0.2–7.7 wt% NaCl equiv. Type 3 inclusions are carbonic inclusions with variable relative content of CO₂ and CH₄, and minor amounts of N₂ and H₂O. The close association of CO₂-rich inclusions and H₂O-rich inclusions in groups and along the same trail suggests the presence of fluid immiscibility. The calculated δ¹⁸O_H2O values range from 4.3‰ to 8.3‰ and δD_H2O values of fluid inclusions vary from −55.8‰ to −46.9‰. A metamorphic origin is preferred on the basis of geological background and analogies with other similar deposit types.Two ore-related sericite samples yield well-defined ⁴⁰Ar/³⁹Ar plateau ages of 425.7 ± 1.7 Ma and 425.2 ± 1.3 Ma, respectively. These data overlap the duration of the Caledonian gold mineralization along the Jiangnan orogen, and suggest that gold mineralization was post-peak regional metamorphism and occurred during the later stages of the Caledonian orogeny.Overall, the Pingqiu gold deposit displays many of the principal characteristics of the Bendigo gold mines in the western Lachlan Orogen (SE Australia) and the Dufferin gold deposit in the Meguma Terrane (Nova Scotia, Canada) but also some important differences, which may lead to the disparity in gold endowment. However, the structural make-up at deposit scale, and the shallow mining depth at present indicate that the Pingqiu gold deposit may have considerable gold potential at depth.     

Constraints on the mineralization processes of the Makeng iron deposit,eastern China: Fluid inclusion,H–O isotope and magnetite trace element analysis

The Makeng iron deposit is located in the Yong’an-Meizhou depression belt in Fujian Province, eastern China. Both skarn alteration and iron mineralization are mainly hosted within middle Carboniferous-lower Permian limestone. Five paragenetic stages of skarn formation and ore deposition have been recognized: Stage 1, early skarn (andradite–grossular assemblage); Stage 2, magnetite mineralization (diopside–magnetite assemblage); Stage 3, late skarn (amphibole–chlorite–epidote–johannsenite–hedenbergite–magnetite assemblage); Stage 4, sulfide mineralization (quartz–calcite–fluorite–chlorite–pyrite–galena–sphalerite assemblage); and Stage 5, carbonate (quartz–calcite assemblage). Fluid inclusion studies were carried out on inclusions in diopside from Stage 2 and in quartz, calcite, and fluorite from Stage 4.Halite-bearing (Type 1) and coexisting two-phase vapor-rich aqueous (Type 3) inclusions in the magnetite stage display homogenization temperatures of 448–564 °C and 501–594 °C, respectively. Salinities range from 26.5 to 48.4 and 2.4 to 6.9 wt% NaCl equivalent, respectively. Two-phase liquid-rich aqueous (Type 2b) inclusions in the sulfide stage yield homogenization temperatures and salinities of 182–343 °C and 1.9–20.1 wt% NaCl equivalent. These fluid inclusion data indicate that fluid boiling occurred during the magnetite stage and that fluid mixing took place during the sulfide stage. The former triggered the precipitation of magnetite, and the latter resulted in the deposition of Pb, Zn, and Fe sulfides. The fluids related to magnetite mineralization have δ¹⁸O_fluid-VSMOW of 6.7–9.6‰ and δD of −96 to −128‰, which are interpreted to indicate residual magmatic water from magma degassing. In contrast, the fluids related to the sulfide mineralization show δ¹⁸O_fluid-VSMOW of −0.85 to −1.04‰ and δD of −110 to −124‰, indicating that they were generated by the mixing of magmatic water with meteoric water. Magnetite grains from Stage 2 exhibit oscillatory zoning with compositional variations in major elements (e.g., SiO₂, Al₂O₃, CaO, MgO, and MnO) from core to rim, which is interpreted as a self-organizing process rather than a dissolution-reprecipitation process. Magnetite from Stage 3 replaces or crosscuts early magnetite, suggesting that later hydrothermal fluid overprinted and caused dissolution and reprecipitation of Stage 2 magnetite. Trace element data (e.g., Ti, V, Ca, Al, and Mn) of magnetite from Stages 2 and 3 indicate a typical skarn origin.     

Silver-base metal epithermal vein and listwanite hosted deposit Crnac,Rogozna Mts., Kosovo,part II: A link between magmatic rocks and epithermal mineralization

Crnac is an intermediate sulfidation Pb–Zn–Ag epithermal deposit located within the Vardar suture zone of the Central Balkan Peninsula. The epithermal Pb–Zn–Ag mineralization consists of (i) a series of steeply-dipping veins hosted within the Jurassic amphibolites, and (ii) overlying hydrothermal-explosive breccia with angular (level IV) or rounded fragments of listwanite (surface) cemented by epithermal mineralization. The mineralization is related to the Oligocene quartz latite dykes that crosscut the Crnac antiform. Quartz latite rocks predominantly display a shoshonitic character. The obtained ⁴⁰Ar/³⁹Ar age of fresh quartz latite is 28.9 ± 0.3 Ma. Fine-grained sericite from altered quartz latite is dated at 28.6 ± 0.5 Ma. Early, alteration related fluid inclusions within quartz latite show coexistence of high-density brine and a low-density vapor-saturated phase that homogenized at 280–405 °C. Phase separation occurs at a paleodepth of 0.6 to 0.9 km.Epithermal mineralization developed in three stages: (i) early pyrite–arsenopyrite–pyrrhotite–quartz–kaolinite; (ii) main sphalerite–galena–tetrahedrite–chalcopyrite and (iii) late carbonate–pyrite–arsenopyrite assemblage. The onset of mineral deposition within epithermal veins was initiated by boiling of Na–Cl ± K ± Ca ± Mg fluid at a paleodepth of 0.6 to 0.9 km. Coexisting vapor and liquid-rich inclusions display salinities and trapping temperatures of 4 wt.% NaCl equiv., 280–370 °C and 2–27 wt.% NaCl equiv., 230–375 °C, respectively. Boiling continued throughout the deposition of the sphalerite-galena-tetrahedrite-chalcopyrite assemblage. Late stage carbonate was deposited from diluted, non-boiling, low-temperature Na–Ca–Mg–Cl ± CO₂ fluid (0.2 to 4.8 wt.% NaCl equiv., 115–280 °C).About 100–150 m higher in the system, precipitation of listwanite breccia cement began as a result of boiling Na–Cl ± Ca ± Mg ± K fluid of medium salinities (2.6 to 12.1 wt.% NaCl equiv.) at temperatures of 245–370 °C. Boiling and dilution of fluids continue throughout the precipitation of the main sphalerite-galena-tetrahedrite and late, mainly carbonate assemblage. Surface listwanite breccia contain quartz phenocrysts deposited from a homogeneous fluid with a medium salinity (8–10 wt.% NaCl equiv.) and high temperatures (T_h = 295–315 °C), whereas the early and main stage of a surface listwanite breccia cement precipitated from a boiling fluid of decreasing salinity and temperature. Aqueous ± CO₂, high salinity (16 to 18 wt.% NaCl equiv.), low temperature (120 °C), homogeneously trapped fluid that precipitated late stage carbonates, is most likely a remnant of boiled off fluid. The epithermal assemblage of the surface listwanites precipitated at a paleodepth of 0.4 to 0.6 km.The δ¹³C values of the late stage ankerite range from − 4.2 to 4.1‰, whereas δ¹⁸O range from 9.6 to 17.5‰. The calculated δ¹⁸O of fluid that precipitated carbonates within epithermal veins, and listwanite breccia cement range from 6.3 to 11.3‰, indicating a contribution of magmatic water.Deposition of all mineralization types was initiated by neutralization of primary acidic magmatic fluid by water-rock reactions that caused widespread propylitization and sericitization. Extensive and long-lasting boiling combined with dilution by meteoric water increased the pH towards the final stage of hydrothermal activity.     

Metallogeny of the Shilu Fe–Co–Cu deposit,Hainan Island,South China: Constraints from fluid inclusions and stable isotopes

The Shilu deposit is a world-class Fe–Co–Cu orebody located in the Changjiang area of the western part of Hainan Island, South China. The distribution of Fe, Co, and Cu orebodies is controlled by strata of the No. 6 Formation in the Shilu Group and the Beiyi synclinorium. Based on a petrological study of the host rocks and their alteration assemblages, and textural and structural features of the ores, four mineralization stages have been identified: (1) the sedimentary ore-forming period; (2) the metamorphic ore-forming period; (3) the hydrothermal mineralization comprising the skarn and quartz–sulfide stage; and (4) the supergene period. The fluid inclusions in sedimentary quartz and/or chert indicate low temperatures (ca. 160 °C) and low salinities from 0.7 to 3.1 wt.% NaCl_eq, which corresponds to densities of 0.77 to 0.93 g/cm³. CO₂-bearing or carbonic inclusions have been interpreted to result from regional metamorphism. Homogenization temperatures of fluid inclusions for the skarn stage have a wide range from 148 °C to 497 °C and the salinities of the fluid inclusions range from 1.2 to 22.3 wt.% NaCl_eq, which corresponds to densities from 0.56 to 0.94 g/cm³. Fluid inclusions of the quartz–sulfide stage yield homogenization temperatures of 151–356 °C and salinities from 0.9 to 8.1 wt.% NaCl_eq, which equates to fluid densities from 0.63 to 0.96 g/cm³.Sulfur isotopic compositions indicate that sulfur of the sedimentary anhydrite and Co-bearing pyrite, and the quartz–sulfide stage, was derived from seawater sulfate and thermochemical sulfate reduction of dissolved anhydrite at temperatures of 200 °C and 300 °C, respectively. H and O isotopic compositions of the skarn and quartz–sulfide stage demonstrate that the ore-forming fluids were largely derived from magmatic water, with minor inputs from metamorphic or meteoric water. The Shilu iron ore deposit has an exhalative sedimentary origin, but has been overprinted by regional deformation and metamorphism. The Shilu Co–Cu deposit has a hydrothermal origin and is temporally and genetically associated with Indosinian granitoid rocks.     

Influence of crude oil on the genesis of the Lanjiagou porphyry molybdenum deposit,western Liaoning Province,China

The Lanjiagou porphyry molybdenum deposit in western Liaoning Province, China, is hosted in fine-grained Jurassic granites. LA-ICP-MS zircon U–Pb analyses indicate that the crystallization of the ore-hosting granites took place 185.0 ± 1.8 Ma (MSWD = 1.4). Molybdenum mineralization in the deposit can be divided into three stages: the stockwork quartz vein stage, the planar quartz vein stage, and the fissure-filling quartz vein stage. Re–Os isotopic ages for the molybdenite from the stockwork quartz vein-type ores yielded an isochron age of 188.8 ± 9.9 Ma (MSWD = 3.0), while six samples from the planar quartz vein-type ores yielded a similar isochron age of 185.6 ± 1.2 Ma (MSWD = 0.5). Re–Os isotopic ages for the molybdenite identical, within error, to zircon U–Pb isotopic ages indicate that the molybdenum mineralization is related to the host intrusions. Apart from primary inorganic fluid inclusions (IFIs), a large number of primary organic fluid inclusions (OFIs) are found in the latter two stages of vein quartz, and minors found in the first stage. The components and characteristics of OFIs in the three stages of vein quartz differ from each other, which is also true for the IFIs. OFIs in stockwork vein quartz are characterized by halite-bearing inclusions, and organic liquids in the inclusions are brown and do not fluoresce under ultraviolet (UV) light. Homogenization temperatures (T_h) for the primary IFIs coeval with OFIs of this stage ranges from 300 °C to > 450 °C, while the salinity varies from 10 to 53 wt.% NaCl equiv.. In planar vein quartz, OFIs are predominately two-phased (liquid and gas), and salt daughter minerals (halite) are absent. Organic liquids are light brown to colorless and show blue fluorescence under UV light; The T_h range for the IFIs of this stage is 250–360 °C, and the salinity range is 3–17 wt.% NaCl equiv. Finally, OFIs in fissure-filling vein quartz are marked by liquid–gas inclusions. Organic liquids are generally colorless and show yellow fluorescence under UV light. The T_h range for the primary IFIs is 180–240 °C and the salinity range is 4–11 wt.% NaCl equiv. Organic geochemical analyses indicate that organic matter in the Lanjiagou deposit was derived from mature crude oil. We suggest that large volumes of crude-oil-bearing non-magmatic fluids were flushed into the Lanjiagou porphyry hydrothermal system during all phases of ore formation and likely played important roles in mineralization.     

Fluid Inclusion,H-O,S, Pb and noble gas isotope studies of the Aerhada Pb-Zn-Ag deposit,Inner Mongolia,NE China

The Aerhada Pb-Zn-Ag deposit is located in the western segment of the Great Hinggan Range Ag-Pb-Zn-Cu-Mo-Au-Fe metallogenic belt in NE China. Orebodies occur mainly as vein type and are hosted by sandstone and siliceous slate. Three stages of primary mineralization, including an early arsenopyrite-pyrite-quartz, a middle polymetallic and silver sulfides-quartz and a late sphalerite-pyrite-calcite-fluorite are recognized. Four types of fluid inclusions have been identified in the ore-bearing quartz and fluorite veins, i.e., liquid-rich, gas-rich, three-phase CO₂ aqueous inclusions, and pure gas or liquid aqueous inclusions. Microthermometric studies on fluid inclusions reveal that homogenization temperatures from early to late stages range from 253° to 430 °C, 195° to 394 °C and 133° to 207 °C, respectively. Fluid salinities range from 2.9 to 14.0 wt.% NaCl equiv. The vapor composition of the ore fluid is dominated by H₂O, CO₂ and CH₄, with minor proportions of N₂. The fluid δ¹⁸O_H2O and δD_H2O values vary from +1.6 to +9.3‰ and −122 to −56‰, respectively, and reflect a magmatic fluid and a meteoric fluid dominant hydrothermal system for the early and late stages of mineralization, respectively. The calculated δ³⁴S_H2S values of hydrothermal fluids in equilibrium with sulfides range from +5.2 to +7.1‰, suggesting a mixed source for sulfur, i.e., the local magmatic and sedimentary rocks. The Pb isotope compositions of sulfides are similar to those of the local magmatic and sedimentary rocks, implying that lead and possibly silver relate to these sources. The noble gas isotope compositions of fluid inclusions hosted in ore minerals suggest that the ore-forming fluids were dominantly derived from a deep mantle source. Fluid mixing and dilution are inferred as the dominant mechanisms for ore deposition. The Aerhada Pb-Zn-Ag deposit can be classified as a medium to low temperature hydrothermal vein type deposit.     

Geology,geochemistry and genesis of the Qianfanling quartz-vein Mo deposit in Songxian County,Western Henan Province,China

The Qianfanling Mo deposit, located in Songxian County, western Henan province, China, is one of the newly discovered quartz-vein type Mo deposits in the East Qinling–Dabie orogenic belt. The deposit consists of molybdenite in quartz veins and disseminated molybdenite in the wall rocks. The alteration types of the wall rocks include silicification, K-feldspar alteration, pyritization, carbonatization, sericitization, epidotization and chloritization. On the basis of field evidence and petrographic analysis, three stages of hydrothermal mineralization could be distinguished: (1) pyrite–barite–quartz stage; (2) molybdenite–quartz stage; (3) quartz–calcite stage.Two types of fluid inclusions, including CO₂-bearing fluid inclusions and water-rich fluid inclusions, have been recognized in quartz. Homogenization temperatures of fluid inclusions vary from 133 °C to 397 °C. Salinity ranges from 1.57 to 31.61 wt.% NaCl eq. There are a large number of daughter mineral-CO₂-bearing inclusions, which is the result of fluid immiscibility. The ore-forming fluids are medium–high temperature, low to moderate salinity H₂O–NaCl–CO₂ system. The δ³⁴S values of pyrite, molybdenite, and barite range from − 9.3‰ to − 7.3‰, − 9.7‰ to − 7.3‰ and 5.9‰ to 6.8‰, respectively. The δ¹⁸O values of quartz range from 9.8‰ to 11.1‰, with corresponding δ¹⁸O_fluid values of 1.3‰ to 4.3‰, and δ¹⁸D values of fluid inclusions of between − 81‰ and − 64‰. The δ¹³C_V-PDB values of fluid inclusions in quartz and calcite have ranges of − 6.7‰ to − 2.9‰ and − 5.7‰ to − 1.8‰, respectively. Sulfur, hydrogen, oxygen and carbon isotope compositions show that the sulfur and ore-forming fluids derived from a deep-seated igneous source. During the peak collisional period between the North China Craton and the Yangtze Craton, the ore-forming fluids that derived from a deep igneous source extracted base and precious metals and flowed upwards through the channels that formed during tectonism. Fluid immiscibility and volatile exsolution led to the crystallization of molybdenite and other minerals, and the formation of economic orebodies in the Qianfanling Mo deposit.     

Metamorphosed Pb–Zn–(Ag) ores of the Keketale VMS deposit,NW China: Evidence from ore textures,fluid inclusions,geochronology and pyrite compositions

The Keketale Pb–Zn deposit is located in the Devonian volcanic-sedimentary Maizi basin of the Altay orogenic belt. The mineralization at Keketale is hosted in marbles and deformed volcanic tuffs and biotite–garnet–chlorite schists, folded into a series of overturned synclines formed in multiple deformation events. Keketale contains economic amounts of Pb (0.89 Mt @ 1.51 wt.%), Zn (1.94 Mt @ 3.16 wt.%) and Ag (650 t @ 40 g/t).Detailed petrographic studies have defined two main generations of sulfide development. The banded pyrite of the early Stage A is commonly stratiform, with minor galena, sphalerite and chalcopyrite. Stage B is characterized by a large amount of polymetallic sulfides including pyrrhotite, chalcopyrite, sphalerite and galena, with minor pyrite hosted in quartz veins.Three types of fluid inclusions (FIs), including mixed carbonic-aqueous (C-type), pure carbonic (PC-type) and aqueous (W-type), have been recognized in quartz of stage B. The C-type FIs have homogenization temperatures of 150–326 °C and salinities of 0.2–16.6 wt.% NaCl equivalent. The PC-type FIs are dominated by CO₂ with minor CH₄ and N₂ and have initial ice-melting temperatures of − 57.5 to − 56.7 °C, CO₂ homogenization temperatures of 11–14.1 °C. The W-type primary FIs were completely homogenized at temperatures of 124–359 °C with salinities of 5.0–14.6 wt.% NaCl equivalent. Such CO₂-rich fluid inclusions are consistent with those discovered in orogenic-type deposits in the Altay area and elsewhere.Muscovite separates from the polymetallic quartz veinlets of stage B yield a well-defined ⁴⁰Ar/³⁹Ar isotopic plateau age of 259.33 ± 2.56 Ma, with an isochron age of 259.62 ± 2.65 Ma. This age is coeval with the closure of the Paleo-Asia Ocean and reactivation of the Ertix Fault system.LA-ICP-MS analyses of two generations of pyrite indicate that the banded pyrite of stage A is relatively depleted in metallic elements and contains low contents of Cu (0.39 ppm), Ag (0.20 ppm), Au (below the detection limits), Pb (17.43 ppm) and Zn (14.38 ppm); whereas the pyrite in quartz–polymetallic sulfide veinlets of the stage B is relatively rich in metallic elements, e.g., Cu (2.56 ppm), Ag (3.07 ppm), Au (0.01 ppm), Pb (1047 ppm) and Zn (1136 ppm). The trace amounts of Cu, Pb, Zn, Au and Ag are interpreted to have been initially locked in the lattice of type-A pyrite, and then liberated and precipitated as micromineral inclusions with type-B pyrite during subsequent metamorphism and deformation.Two key factors are considered vital to the formation of economic ores of the Keketale Pb–Zn deposit, namely the original Devonian banded pyrite formed in a VMS system and subsequent Permian deformation and metamorphic processes that liberated Cu, Pb, Zn, Au and Ag from the lattice of type-A pyrite to form galena, sphalerite and chalcopyrite with minor muscovite in quartz veinlets. The model provides a new interpretation of VMS Pb–Zn deposit occurring in back-arc basin environments followed by collision, and new insights into the unique regional Fe–Cu–Pb–Zn–Au mineralization in the Altay orogenic belt.     

Genesis of the Proterozoic Mangabeira tin–indium mineralization,Central Brazil: Evidence from geology,petrology, fluid inclusion and stable isotope data

The Mangabeira deposit is the only known Brazilian tin mineralization with indium. It is hosted in the Paleo- to Mesoproterozoic Mangabeira within-plate granitic massif, which has geochemical characteristics of NYF fertile granites. The granitic massif is hosted in Archean to Paleoproterozoic metasedimentary rocks (Ticunzal formation), Paleoproterozoic peraluminous granites (Aurumina suite) and a granite–gneiss complex. The mineralized area comprises evolved Li-siderophyllite granite, topaz–albite granite, Li–F-rich mica greisens and a quartz–topaz rock, similar to topazite. Two types of greisens are recognized in the mineralized area: zinnwaldite greisen and Li-rich muscovite greisen, formed by metasomatism of topaz–albite granite and Li-siderophyllite granite, respectively. Cassiterite occurs in the quartz–topaz rock and in the greisens. Indium minerals, such as roquesite (CuInS₂), yanomamite (InAsO₄·2H₂O) and dzhalindite (In(OH₃)), and In-rich cassiterite, sphalerite, stannite group minerals and scorodite are more abundant in the quartz–topaz rock, and are also recognized in albitized biotite granite and in Li-rich muscovite greisen. The host rocks and mineralized zones were subsequently overprinted by the Brasiliano orogenic event.Primary widespread two-phase aqueous and rare coeval aqueous-carbonic fluid inclusions are preserved in quartz from the topaz–albite granite, in quartz and topaz from the quartz–topaz rock and in cassiterite from the Li-rich muscovite greisen. Eutectic temperatures are − 25 °C to − 23 °C, allowing modeling of the aqueous fluids in the system H₂O–NaCl(–KCl). Rare three-phase H₂O–NaCl fluid inclusions (45–50 wt.% NaCl equiv.) are restricted to the topaz–albite granite. Salinities and homogenization temperatures of the aqueous and aqueous-carbonic fluid inclusions decrease from the topaz–albite granite (15–20 wt.% NaCl equiv.; 400 °C–450 °C), to the quartz–topaz rock (10–15 wt.% NaCl equiv.; 250 °C–350 °C) and to the greisen (0–5 wt.% NaCl equiv.; 200 °C–250 °C). Secondary fluid inclusions have the same range of salinities as the primary fluid inclusions, and homogenize between 150 and 210 °C.The estimated equilibrium temperatures based on δ¹⁸O of quartz–mica pairs are 610–680 °C for the topaz–albite granite and 285–370 °C for the Li-rich muscovite greisens. These data are coherent with measured fluid inclusion homogenization temperatures. Temperatures estimated using arsenopyrite geothermometry yield crystallization temperatures of 490–530 °C for the quartz–topaz rock and 415–505 °C for the zinnwaldite greisens. The fluids in equilibrium with the topaz–albite granite have calculated δ¹⁸O and δD values of 5.6–7.5‰ and − 67 to − 58‰, respectively. Estimated δ¹⁸O and δD values are mainly 4.8–7.9‰ and − 60 to − 30‰, respectively, for the fluids in equilibrium with the quartz–topaz rock and zinnwaldite greisen; and 3.4–3.9‰ and − 25 to − 17‰, respectively, for the Li-rich muscovite greisen fluid. δ³⁴S data on arsenopyrite from the quartz–topaz rock vary from − 1.74 to − 0.74‰, consistent with a magmatic origin for the sulfur. The integration of fluid inclusion with oxygen isotopic data allows for estimation of the minimum crystallization pressure at ca. 770 bar for the host topaz–albite granite, which is consistent with its evolved signature.Based on petrological, fluid inclusion and isotope data it is proposed that the greisens and related Mangabeira Sn–In mineralization had a similar hydrothermal genesis, which involved exsolution of F-rich, Sn–In-bearing magmatic fluids from the topaz–albite granite, early formation of the quartz–topaz rock and zinnwaldite greisen, progressive cooling and Li-rich muscovite greisen formation due to interaction with meteoric water. The quartz–topaz rock is considered to have formed in the magmatic-hydrothermal transition. The mineralizing saline and CO₂-bearing fluids are interpreted to be of magmatic origin, based on the isotopic data and paragenesis, which has been documented as characteristic of the tin mineralization genetically related to Proterozoic within-plate granitic magmatism in the Goias Tin Province, Central Brazil.     

Whole rock geochemistry,molybdenite Re-Os geochronology,stable isotope and fluid inclusion investigations of the Siah-Kamar deposit,western Alborz-Azarbayjan: New constrains on the porphyry Mo deposit in Iran

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 δ¹⁸O_water 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.     

The Jiguanshan porphyry Mo deposit in the Xilamulun metallogenic belt,northern margin of the North China Craton,U–Pb geochronology,isotope systematics,geochemistry and fluid inclusion studies: Implications for a genetic model

The Jiguanshan porphyry Mo deposit is located in the southern part of Xilamulun metallogenic belt at the northern margin of the North China Craton (NCC). In the Jiguanshan mining district, two stages of granitoids intrusions have been recognized: a pre-ore granite porphyry with stockworks and veins of Mo mineralization, and a granite porphyry with disseminated Mo mineralization. Zircon U–Pb data and Hf isotope analyses show that the dissemination-mineralized granite porphyry yielded a weighted mean ²⁰⁶Pb/²³⁸U age of 156.0 ± 1.3 Ma, with a crustal ε_Hf(t) values from − 5.6 to + 0.2, and that the main group of magmatic zircons from the pre-ore granite porphyry have a weighted mean ²⁰⁶Pb/²³⁸U age of 167.7 ± 1.7 Ma with ε_Hf(t) values from − 3.2 to + 1.0. Combined with groundmass Ar–Ar age data of the granite porphyry and molybdenite Re–Os age, it is suggested that the Mo mineralization of Jiguanshan deposit was formed in the late Jurassic (153 ~ 155 Ma) during tectonic and magmatic events that affected northeast China. The Mo mineralization was a little bit later than the host granite porphyry. Besides disseminated in the host granite porphyry, Mo mineralization also presents in middle Jurassic pre-ore granite porphyry, Jurassic fine-grained diabase, Triassic quartz porphyry, and in rhyolitic volcanic rocks as well as syenite of Devonian age.The Jiguanshan mining district was affected by the tectonic events associated with the Paleo-Asian Ocean closure, and later by far-field tectonism, related to subduction of the Paleo-Pacific plate (Izanagi) in the Jurassic-Cretaceous. The tectonic and thermal events linked with the latter are commonly referred to as Yanshanian tectono-thermal event, and consists of a series of geodynamic, magmatic and ore-forming processes, which in the mining district area included the intrusion of the pre-ore granite porphyry, the host granite porphyry, Mo mineralization, and fine-grained diabase. Major and trace element analyses show that the host granite porphyry is characterized by high silica abundances (SiO₂ = 77.16 to 77.51%), high Rb/Sr ratios (13.57 to 14.83), high oxidation (Fe₂O₃/FeO = 34.25 to 62.00) and high alkalies (Na₂O + K₂O = 8.21 to 8.38%). Petrographic and microthermometry studies of the fluid inclusions from Mo mineralized veins, characterized by plenty of daughter mineral-bearing inclusions, showed that the predominant homogenization temperatures range from 250 to 440 °C. Combined with Laser Raman analysis of the fluid inclusions, it is indicated that Mo mineralization is related to a high-temperature, hypersaline and high-oxygen fugacity H₂O–NaCl fluid system, with high F contents.Based on geology, geochronology, isotope systematics, geochemistry and fluid inclusion studies as well as regional geology, we propose, for the first time, a genetic model for the Jiguanshan porphyry Mo deposit. During the Jurassic geodynamic evolution of northeast China, high silicic, high oxidized and alkaline-rich granitic magma probably derived from partial melting of the lower crust, episodically intruded along faults into the country rocks. This fluid system, fractionating from the highly differentiated granitic magma and bearing Mo with minor Cu metals, migrated upwards and interacted with the older wall rocks and associated fractures, in which the ore minerals precipitated, resulting in the development of what we refer to as the “Jiguanshan-type” porphyry Mo deposit.