Genesis of the Fuxing porphyry Cu deposit in Eastern Tianshan,China: Evidence from fluid inclusions and C–H–O–S–Pb isotope systematics

The Fuxing porphyry Cu deposit is a recently discovered deposit in Eastern Tianshan, Xinjiang, northwestern China. The Cu mineralization is associated with the Fuxing plagiogranite porphyry and monzogranite, mainly presenting as various types of hydrothermal veins or veinlets in alerted wall rocks, with potassic, chlorite, phyllic, and propylitic alteration developed. The ore-forming process can be divided into four stages: stage I barren quartz veins, stage II quartz–chalcopyrite–pyrite veins, stage III quartz–polymetallic sulfide veins and stage IV quartz–calcite veins. Four types of fluid inclusions (FIs) can be distinguished in the Fuxing deposit, including hypersline (H-type), vapor-rich two-phase (V-type), liquid-rich two-phase (L-type), and trace amounts of pure vapor inclusions (P-type), but only the stage I quartz contains all types of FIs. The stages II and III quartz have two types of FIs, with exception of H- and P-types. In stage IV quartz minerals, only the L-type inclusions can be observed. The FIs in quartz of stages I, II, III and IV are mainly homogenized at temperatures of 357–518 °C, 255–393 °C, 234–322 °C and 145–240 °C, with salinities of 1.9–11.6 wt.% NaCl equiv., 1.6–9.6 wt.% NaCl equiv., 1.4–7.7 wt.% NaCl equiv. and 0.9–3.7 wt.% NaCl equiv., respectively. The ore-forming fluids of the Fuxing deposit are characterized by high temperature, moderate salinity and relatively oxidized condition. Carbon, hydrogen and oxygen isotopic compositions of quartz indicate that the ore-forming fluids were gradually evolved from magmatic to meteoric in origin. Sulfur and lead isotopes suggest that the ore-forming materials were derived from a deep-seated magma source. The Cu mineralization in the Fuxing deposit occurred at a depth of ~ 1 km, and the changes of oxygen fugacity, decompression boiling, and local mixing with meteoric water were most likely critical for the formation of the Fuxing Cu deposit.     

Metallogenesis and ore-forming time of the Changtuxili Mn–Ag–Pb–Zn deposit in Inner Mongolia: Evidence from C–O–S isotopes and U–Pb geochronology

This paper reports new geochronological (U–Pb) and isotope (C, O, and S) data to investigate the timing of mineralization and mode of ore genesis for the recently discovered Changtuxili Mn–Ag–Pb–Zn deposit, located on the western slopes of the southern Great Hinggan Range in NE China. The mineralization is hosted by intermediate–acidic lavas and pyroclastic rocks of the Baiyingaolao Formation. Three stages of mineralization are identified: quartz–pyrite (Stage I), galena–sphalerite–tetrahedrite–rhodochrosite (Stage II), and quartz–pyrite (Stage III). δ¹³C and δ¹⁸O values for carbonate from the ore vary from −8.51‰ to −4.96‰ and 3.97‰ to 15.90‰, respectively, which are indicative of a low-temperature alteration environment. δ³⁴S_V-CDT values of sulfides range from −1.77‰ to 4.16‰ and show a trend of equilibrium fractionation (δ³⁴S_Py ​> ​δ³⁴S_Sp ​> ​δ³⁴S_Gn). These features indicate that pyrite, sphalerite, and galena precipitated during the period of mineralization. The alteration mineral assemblage and isotope data indicate that the weakly acidic to weakly alkaline ore-forming fluid was derived largely from meteoric water and the ore-forming elements C and S originated from magma. During the mineralization, a geochemical barrier was formed by changes in the pH of the ore-forming fluid, leading to the precipitation of rhodochrosite. On the basis of the mineralization characteristics, new isotope data, and comparison with adjacent deposits, we propose that the Changtuxili Mn–Ag–Pb–Zn deposit is an intermediate-to low-sulfidation epithermal deposit whose formation was controlled by fractures and variability in the pH of the ore-forming fluid. The surrounding volcanic rocks yield zircon U–Pb ages of 160−146 ​Ma (Late Jurassic), indicating that the mineralization is younger than 146 ​Ma.     

SHRIMP zircon U–Pb geochronology,geochemistry and H–O–Si–S–Pb isotope systematics of the Kanggur gold deposit in Eastern Tianshan,NW China: Implication for ore genesis

The Kanggur gold deposit is located in the southern margin of the Central Asia Orogenic Belt and in the western segment of the Kanggur–Huangshan ductile shear belt in Eastern Tianshan, northwestern China. The orebodies of this deposit are hosted in the Lower Carboniferous volcanic rocks of the Aqishan Formation and mainly consist of andesite, dacite and pyroclastic rocks. The SHRIMP zircon U–Pb age data of the andesite indicate that the volcanism in the Kanggur area might have occurred at ca. 339 Ma in the Early Carboniferous, and that the mineralization age of the Kanggur gold deposit was later than the age of volcanic rocks in the area. Geochemically, the andesite rocks of the Aqishan Formation belong to low-tholeiite and calc-alkaline series and display relative depletions in high field strength elements (HFSEs; i.e. Nb, Ta and Ti). The δ¹⁸O_w and δD_w values vary from − 9.1‰ to + 3.8‰ and − 66.0‰ to − 33.9‰, respectively, indicating that the ore-forming fluids were mixtures of metamorphic and meteoric waters. The δ³⁰Si values of 13 quartz samples range from − 0.3‰ to + 0.1‰ with an average of − 0.15‰, and the δ³⁴S values of 18 sulphide samples range from − 0.9‰ to + 2.2‰ with an average of + 0.54‰. The ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb values of 10 sulphide samples range from 18.166 to 18.880, 15.553 to 15.635 and 38.050 to 38.813, respectively, showing similarities to orogenic Pb; these values are consistent with those of the andesite from the Kanggur area, suggesting a common lead source. All of the silicon, sulphur and lead isotopic systems indicate that the ore-forming fluids and materials were mainly derived from the Aqishan Formation, and that the host volcanic rocks of the Aqishan Formation probably played a significant role in the Kanggur gold mineralization. Integrating the data obtained from studies on geology, geochronology, petro-geochemistry and H–O–Si–S–Pb isotope systematics, we suggest that the Kanggur gold deposit is an orogenic-type deposit formed in Eastern Tianshan orogenic belt during the Permian post-collisional tectonism.     

Fluid inclusions and H–O–S–Pb isotope systematics of the Baishan porphyry Mo deposit in Eastern Tianshan,China

The Baishan porphyry Mo deposit formed in the Middle Triassic in Eastern Tianshan, Xinjiang, northwestern China. Mo mineralization is associated with the Baishan monzogranite and granite porphyry stocks, mainly presenting as various types of hydrothermal veinlets in alerted wall rocks, with potassic, phyllic, propylitic, and fluorite alteration. The ore-forming process can be divided into four stages: stage I K-feldspar–quartz–pyrite veinlets, stage II quartz–molybdenite ± pyrite veinlets, stage III quartz–polymetallic sulfide veinlets and stage IV barren quartz–calcite veins. Four types of fluid inclusions (FIs) can be distinguished in the Baishan deposit, namely, liquid-rich two-phase (L-type), vapor-rich two-phase (V-type), solid-bearing multi-phase (S-type) and mono-phase vapor (M-type) inclusions, but only the stage I quartz contains all types of FIs. The stages II and III quartz have three types of FIs, with exception of M-type. In stage IV quartz minerals, only the L-type inclusions can be observed. The FIs in quartz of stages I, II, III and IV are mainly homogenized at temperatures of 271–468 °C, 239–349 °C, 201–331 °C and 134–201 °C, with salinities of 2.2–11.6 wt.% NaCl equiv., 1.1–10.2 wt.% NaCl equiv., 0.5–8.9 wt.% NaCl equiv. and 0.2–5.7 wt.% NaCl equiv., respectively. The ore-forming fluids of the Baishan deposit are characterized by high temperature, moderate salinity and relatively reduced condition, belonging to a H₂O–NaCl ± CH₄ ± CO₂ system. Hydrogen and oxygen isotopic compositions of quartz indicate that the ore-forming fluids were gradually evolved from magmatic to meteoric in origin. Sulfur and lead isotopes suggest that the ore-forming materials came predominantly from a deep-seated magma source from the lower continental crust. The Mo mineralization in the Baishan deposit is estimated to have occurred at a depth of no less than 4.7 km, and the decrease in temperature and remarkable transition of the redox condition (from alkalinity to acidity) of ore-forming fluids were critical for the formation of the Baishan Mo deposit.     

Geology,geochemistry and fluid inclusions of the Bianjiadayuan Pb–Zn–Ag deposit,Inner Mongolia,NE China: Implications for tectonic setting and metallogeny

The Bianjiadayuan Pb–Zn–Ag deposit in the Southern Great Xing'an Range consists of quartz-sulfide vein-type and breccia-type mineralization related to granite. Vein orebodies are localized in NW-trending extensional faults. Hydrothermal alteration is well developed and includes silicification, potassic alteration, chloritization and sericitization. Three stages of mineralization are recognized based on field evidence and petrographic observation and are marked by assemblages of quartz–arsenopyrite–pyrite (stage I), quartz–pyrrhotite–chalcopyrite–sphalerite (stage II) and quartz–galena–silver minerals (stage III). The granite, with a zircon age of 143.2 ± 1.5 Ma (n = 14, MSWD = 0.93), is subalkaline, peraluminous and is classified as A2-type granite originating in a post-orogenic extensional setting during the opening of suture zone between the North China Craton and the Siberia Craton from the Late Jurassic to the Early Cretaceous. The δ³⁴S_CDT values of sulfides, ranging from 3.19 to 10.65‰, are not consistent with the majority of magmatic hydrothermal deposits in the SGXR, possibly implying accessory source in addition to magmatic source. Microthermometric measurements show that ore minerals were deposited at intermediate temperatures (347.8–136.4 °C) with moderate salinities (2.9–14.4 wt.% NaCl). Ore-forming fluids were derived largely from magmatic hydrothermal processes, with the addition of meteoric water in late stage. Successive precipitation of Pb, Zn and Ag occurred with changes of physicochemical conditions. Overall considering mineralization features, ore-forming fluids and materials and tectonic setting and comparing with adjacent deposits, the Bianjiadayuan deposit is a mesothermal magmatic hydrothermal vein-type Pb–Zn–Ag deposit controlled by fractures and related to A2-type granite in response to the tectonic/magmatic/hydrothermal activity in late Jurassic. Besides, the explosive breccias in the west area require more attention in future exploration.     

Fluid inclusions and H–O–S–Pb isotope systematics of the Chalukou giant porphyry Mo deposit,Heilongjiang Province,China

The Chalukou giant porphyry Mo deposit, located in the northern Great Xing'an Range, is the largest Mo deposit in the Xing'an–Mongolia orogenic belt. This deposit's ore bodies are mainly hosted in an intermediate–felsic complex and Jurassic volcanic sedimentary rocks, of which Late Jurassic granite porphyry, quartz porphyry and fine grained granite are closely associated with the Mo mineralization. Three types of fluid inclusions (FIs) are present in the quartz associated with oxide and sulphide minerals, i.e., liquid-rich two-phase, gas-rich two-phase and daughter mineral-bearing multiphase FIs. The FIs in the quartz phenocrysts of the granite porphyry contain liquid-rich two-phase, gas-rich two-phase and daughter mineral-bearing multiphase FIs. The homogenization temperatures vary from 230 °C to 440 °C and 470 °C to 510 °C, and their salinities vary from 0.7% to 53.7% NaCl eq. and 6.2% to 61.3% NaCl eq., respectively. The FIs of K-feldspar–quartz–magnetite veins of the early stage are composed of liquid-rich two-phase, gas-rich two-phase and daughter mineral-bearing multiphase FIs with homogenization temperatures and salinities of 320 °C to 440 °C and 4.2% to 52.3% NaCl eq., respectively. The FIs of quartz–molybdenite veins and breccia of the middle stage are composed of liquid-rich two-phase, gas-rich two-phase and daughter mineral-bearing multiphase FIs with homogenization temperatures and salinities of 260 °C to 410 °C and 0.4% to 52.3% NaCl eq., respectively. FIs of quartz–fluorite–galena–sphalerite veins of the late stage are liquid-rich two-phase FIs with homogenization temperatures and salinities of 170 °C to 320 °C and 0.5% to 11.1% NaCl eq., respectively. The ore-forming fluids of the Chalukou deposit are characterised by high temperature, high salinity and high oxygen fugacity, belonging to an F-rich H₂O–NaCl ± CO₂ system. The δ¹⁸O_W values vary from − 4.5‰ to 3.2‰, and the δD_W values vary from − 138‰ to − 122‰, indicating that the ore-forming fluids were a mixture of magmatic and meteoric water. The δ³⁴S values range from − 1.9‰ to + 3.6‰ with an average of + 1.6‰. The ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb values of the metallic minerals are in the ranges of 18.269–18.501, 15.524–15.567 and 38.079–38.264, respectively. Both the S and Pb isotopic systems indicate that the ore metals and fluids came primarily from a deep-seated magma source from the juvenile lower crust. The Mo mineralization in the Chalukou deposit occurred at a depth of 0.5 to 1.3 km, and multiple stages of phase separation or immiscibility of ore-forming fluid was critical for the formation of the Chalukou deposit.     

Geology,C–H–O–S–Pb isotope systematics and geochronology of the Yindongpo gold deposit,Tongbai Mountains,central China: Implication for ore genesis

The Yindongpo gold deposit is located in the Weishancheng Au–Ag-dominated polymetallic ore belt in Tongbai Mountains, central China. The ore bodies are stratabound within carbonaceous quartz–sericite schists of the Neoproterozoic Waitoushan Group. The ore-forming process can be divided into three stages, represented by early barren quartz veins, middle polymetallic sulfide veinlets and late quartz–carbonate stockworks, with most ore minerals, such as pyrite, galena, native gold and electrum being formed in the middle stage. The average δ¹⁸O_water values changed from 9.7‰ in the early stage, through 4.9‰ in the middle stage, to − 5.9‰ in the late stage, with the δD values ranging between − 65‰ and − 84‰. The δ¹³C_CO2 values of ore fluids are between − 3.7‰ and + 6.7‰, with an average of 1.1‰. The H–O–C isotope systematics indicate that the ore fluids forming the Yindongpo gold deposit were probably initially sourced from a process of metamorphic devolatilization, and with time gradually mixed with meteoric water. The δ³⁴S values range from − 0.3‰ to + 5.2‰, with peaks ranging from + 1‰ to + 4‰. Fourteen sulfide samples yield ²⁰⁶Pb/²⁰⁴Pb values of 16.990–17.216, ²⁰⁷Pb/²⁰⁴Pb of 15.419–15.612 and²⁰⁸Pb/²⁰⁴Pb of 38.251–38.861. Both S and Pb isotope ratios are similar to those of the main lithologies of the Waitoushan Group, but differ from other lithologic units and granitic batholiths in the Tongbai area, which suggest that the ore metals and fluids originated from the Waitoushan Group. The available K–Ar and ⁴⁰Ar/³⁹Ar ages indicate that the ore-forming process mainly took place in the period of 176–140 Ma, during the transition from collisional compression to extension and after the closure of the oceanic seaway in the Qinling Orogen. The Yindongpo gold deposit is interpreted as a stratabound orogenic-style gold system formed during the transition phase from collisional compression to extension.The ore metals in the Waitoushan Group were extracted, transported and then accumulated in the carbonaceous sericite schist layer. The carbonaceous sericite schist layer, especially at the junction of collapsed anticline axis and fault structures, became the most favorable locus for the ore bodies.     

Isotopic (C–O–S) geochemistry and Re–Os geochronology of the Haobugao Zn–Fe deposit in Inner Mongolia,NE China

The Haobugao Zn–Fe deposit is a typical skarn deposit located in the southern part of the Great Xing’an Range that hosts polymetallic mineralization over a large region. The main ore minerals at the deposit include sphalerite, magnetite, galena, chalcopyrite and pyrite, and the main gangue minerals include andradite, grossular garnet, hedenbergite, diopside, ilvaite, calcite and quartz. There are broadly two mineralizing periods represented by the relatively older skarn and younger quartz–sulfide veins. In detail, there are five metallogenic stages consisting of an early skarn, late skarn, oxide, early quartz–sulfide, and late quartz–sulfide–calcite stages. Electron microprobe analyses show that the garnet at the deposit varies in composition from And_97.95Gro_0.41Pyr_1.64 to And_30.69Gro_66.69Pyr_2.63, and pyroxene is compositionally in the diopside–hedenbergite range (i.e. Di_90.63Hd_8.00Jo_1.37–Hd_88.98Di_4.53Jo_6.49). Petrographic observations and electron microprobe analyses indicate that the sphalerite has three generations ([Zn_0.93Fe_0.08]S–[Zn_0.75Fe_0.24]S). The Zn associated with the first generation sphalerite replaced Cu and Fe of early xenomorphic granular chalcopyrite (i.e. [Cu_1.01Fe_1.03]S₂–[Cu_0.99Fe_0.99]S₂), and part of the first generation sphalerite is coeval with late chalcopyrite (i.e. [Cu_0.96Fe_0.99Zn_0.03]S₂–[Cu_1.00Fe_1.03Zn_0.01]S₂). Magnetite has a noticeable negative Ce anomaly (δCe = ∼0.17 to 0.54), which might be a result of the oxidized ore-fluid. Thirty δ³⁴S_V-PDB analyses of sulfides from the ore range from −2.3 to −0.1‰ in value, which are indicative of a magmatic source. The δ¹³C‰ and δ¹⁸O‰ values for calcite from the ore formed at quartz–sulfide–calcite stage vary from −9.9 to −5.5‰ and from −4.2 to 1.1‰, respectively, contrasting with δ¹³C‰ (2.9–4.8‰) and δ¹⁸O‰ (9.8–13.9‰) values for calcite from marble. It is suggested that the ore-forming fluid associated with late stage of mineralization was predominantly magmatic in origin with some input of local meteoric water.Molybdenite from the Haobugao deposit defines an isochron age of 142 ± 1 Ma, which is interpreted as the mineralization age being synchronous, within error, with the zircon U–Pb ages of 140 ± 1, 141 ± 2, and 141 ± 1 Ma for granite at the deposit. These data and characteristics of lithology and mineralization further show that the Zn–Fe mineralization is temporally and spatially related to the emplacement of granite in an extensional tectonic setting during the Mesozoic.     

The genesis of the ores and granitic rocks at the Hongshi Au deposit in Eastern Tianshan,China: Constraints from zircon U–Pb geochronology,geochemistry and isotope systematics

The Hongshi gold deposit is located in the southwestern margin of the Kanggur–Huangshan ductile shear zone in Eastern Tianshan, Northwest China. The gold ore bodies are predominantly hosted in the volcanogenic metasedimentary rocks of the Lower Carboniferous Gandun Formation and the Carboniferous syenogranite and alkali-feldspar granite. The syenogranite and the alkali-feldspar granite yield SHRIMP zircon U–Pb ages of 337.6 ± 4.5 Ma (2σ, MSWD = 1.3) and 334.0 ± 3.7 Ma (2σ, MSWD = 1.1), respectively, indicating that the Hongshi gold deposit is younger than 334 Ma. The granitoids belong to shoshonitic series and are relatively enriched in large ion lithophile elements (Rb, K, Ba, and Pb) and depleted in high field-strength elements (Nb, Ta, P, and Ti). Moreover, these granitoids have high SiO₂, Al₂O₃, and K₂O contents, low Na₂O, MgO, and TiO₂ contents, low Nb/Ta ratios, and slightly positive Eu anomalies. The ε_Hf(t) values of the zircons from a syenogranite sample vary from + 1.5 to + 8.8 with an average of + 5.6; the ε_Hf(t) values of the zircons from an alkali-feldspar granite sample vary from + 5.0 and + 10.1 with an average of + 7.9. The δ³⁴S values of 10 sulfide samples ranged from − 11.5‰ to + 4.2‰, with peaks in the range of + 1‰ to + 4‰. The above-mentioned data suggest that the Hongshi granitoids were derived from the melting of juvenile lower crust mixed with mantle components formed by the southward subduction of the paleo-Tianshan ocean plate beneath the Aqishan–Yamansu island arc during the Early Carboniferous. The Hongshi gold deposit was formed by post-collisional tectonism during the Permian. The granitoids most likely acted as impermeable barriers that prevented the leakage and runoff of ore-bearing fluids. Thus, the granitoids probably played an important role in controlling gold mineralization.     

Geological and C–O–S–Pb–Sr isotopic constraints on the origin of the Qingshan carbonate-hosted Pb–Zn deposit,Southwest China

Located in the western Yangtze Block, the Qingshan Pb–Zn deposit, part of the Sichuan–Yunnan–Guizhou Pb–Zn metallogenic province, contains 0.3 million tonnes of 9.86 wt.% Pb and 22.27 wt.% Zn. Ore bodies are hosted in Carboniferous and Permian carbonate rocks, structurally controlled by the Weining–Shuicheng anticline and its intraformational faults. Ores composed of sphalerite, galena, pyrite, dolomite, and calcite occur as massive, brecciated, veinlets, and disseminations in dolomitic limestones.

The C–O isotope compositions of hydrothermal calcite and S–Pb–Sr isotope compositions of Qingshan sulphide minerals were analysed in order to trace the sources of reduced sulphur and metals for the Pb–Zn deposit. δ¹³C_PDB and δ¹⁸O_SMOW values of calcite range from –5.0‰ to –3.4‰ and +18.9‰ to +19.6‰, respectively, and fall in the field between mantle and marine carbonate rocks. They display a negative correlation, suggesting that CO₂ in the hydrothermal fluid had a mixed origin of mantle, marine carbonate rocks, and sedimentary organic matter. δ³⁴S values of sulphide minerals range from +10.7‰ to +19.6‰, similar to Devonian-to-Permian seawater sulphate (+20‰ to +35‰) and evaporite rocks (+23‰ to +28‰) in Carboniferous-to-Permian strata, suggesting that the reduced sulphur in hydrothermal fluids was derived from host-strata evaporites. Ores and sulphide minerals have homogeneous and low radiogenic Pb isotope compositions (²⁰⁶Pb/²⁰⁴Pb = 18.561 to 18.768, ²⁰⁷Pb/²⁰⁴Pb = 15.701 to 15.920, and ²⁰⁸Pb/²⁰⁴Pb = 38.831 to 39.641) that plot in the upper crust Pb evolution curve, and are similar to those of Devonian-to-Permian carbonate rocks. Pb isotope compositions suggest derivation of Pb metal from the host rocks. ⁸⁷Sr/⁸⁶Sr ratios of sphalerite range from 0.7107 to 0.7136 and (⁸⁷Sr/⁸⁶Sr)_200Ma ratios range from 0.7099 to 0.7126, higher than Sinian-to-Permian sedimentary rocks and Permian Emeishan flood basalts, but lower than Proterozoic basement rocks. This indicates that the ore strontium has a mixture source of the older basement rocks and the younger cover sequence. C–O–S–Pb–Sr isotope compositions of the Qingshan Pb–Zn deposit indicate a mixed origin of the ore-forming fluids and metals.     

Tracing the ore-formation history of the shear-zone-controlled Huogeqi Cu–Pb–Zn deposit in Inner Mongolia,northern China,using H,O, S,and Fe isotopes

The original ore-fluid of the Huogeqi Cu–Pb–Zn deposit in Inner Mongolia, northern China, was enriched in heavy oxygen isotopes with δ¹⁸O values ranging from 9.9 to 11.4 per mil, which is characteristic of the metamorphic devolatilization of pelitic rocks. The δD values determined by direct measurement of syn-ore hydrothermal tremolite range from − 116 to − 82 per mil, lying between the domains of typical metamorphic fluid and meteoric water, which is in equilibrium with organic matter. Oxygen and hydrogen isotope ratios indicate that the ore-fluid was derived from deep-sourced metamorphic fluid and interacted with organic-rich shale during fluid migration, which is consistent with the fluid evolution history revealed by a previous fluid inclusion study. Sulfides in the deposit are characteristically enriched in heavy S isotopes, with an average δ³⁴S value of 13.4 ± 6.2 per mil (1σ, n = 103). The S-isotope ratios are identical to stratabound sulfides generated through the non-bacterial reduction of Neoproterozoic marine sulfate (with δ³⁴S values of ~ 17 per mil). Previous studies on lead isotopes of sulfides revealed that the ore-forming metals (Cu, Pb, and Zn) at the Huogeqi deposit were also remobilized from a stratabound source. This source was syngenetically elevated in its Cu-, Pb-, and Zn-sulfide content as a result of submarine hydrothermal activities forming sulfide-rich layers within a rift tectonic setting. The Fe isotope ratios for sulfides are consistent with those of an intercalated iron-formation within the ore-hosting rocks, suggesting that the Fe in the sulfides was derived from local host rocks during sulfide precipitation and the Fe-rich rocks are favorable lithological units for high-grade mineralization. The heterogeneous sources of ore-fluid, S, ore-forming metals, and Fe are explained by a multistage genetic model, which is supported by the geological characteristic of the deposit. The enriched sulfides were subsequently remobilized and enriched by metamorphic devolatilization during the Permian and Triassic periods. The metamorphic ore-fluid ascended along a shear zone and interacted with organic-rich shale. Sulfides eventually precipitated within the shear zone at a shallower crustal level, especially where the shear zone intersected Fe-rich host rocks. This multistage genetic model has implications for mineral exploration. Greenschist to amphibolite facies terranes containing thick Neoproterozoic rift sequences are ideal regions for potential Cu–Pb–Zn mineralization. In particular, intercalated volcanic rocks within the rift sequences are indicative of high heat-flow and are ideal for the development of submarine hydrothermal systems. The primary structures hosting mineralization and ore shoots in the Huogeqi area are jogs in the shear zones. In addition, Fe-rich lithological units, such as iron-formations, are ideal hosts for high-grade ore.     

Molybdenite Re–Os and U–Pb zircon dating and genesis of the Dayana W-Mo deposit in eastern Ujumchin,Inner Mongolia

The Dayana W-Mo deposit in eastern Ujumchin of Inner Mongolia is a quartz-vein type deposit in the mid-western part of the Central Asian Orogenic Belt (CAOB). Biotite monzogranite, quartz porphyry and hornfels host W-Mo in quartz veins. Based on spatial relationships, molybdenite was deposited first followed by wolframite. This contribution presents precise laser ablation inductively coupled plasma mass spectroscopy (LA-ICP-MS) U–Pb zircon dating and geochemical analysis of the biotite monzogranite. The U–Pb dating shows that the monzogranite is 134 ± 1 Ma. Major and trace element geochemistry shows that the monzogranite is characterized by high SiO₂ and K₂O contents, a “Right-inclined” shape of the chondrite normalized REE patterns, enrichment of large ion lithophile elements (LILEs), and depletion of high field strength elements (HFSEs) such as Nb, P, Ba. The monzogranite is high-K calc-alkaline, has a strong negative Eu anomaly (Eu/Eu* = 0.04–0.45), low P₂O₅ content, high A/CNK of > 1.2, enriched in large-ion lithophile elements (LILEs; such as Rb, Th, U, Nd, and Hf), and notably depleted in Ba, Sr, P, Ti, and Nb. These characteristics define the Dayana monzogranite as a highly fractionated peraluminous granite. Re–Os isotopic analysis of seven molybdenite samples from the deposit yield an isochron age of 133 ± 3 Ma (MSWD = 2.2), which indicates that the monzogranite and ore have the same age within error, are probably genetically related, and related to a major Early Cretaceous mineralizing event in China known as the Yanshanian.     

Genesis of the Nanyangtian scheelite deposit in southeastern Yunnan Province,China: evidence from mineral chemistry,fluid inclusions,and C–O isotopes

The Nanyangtian skarn-type scheelite deposit is an important part of the Laojunshan W–Sn polymetallic metallogenic region in southeastern Yunnan Province, China. The deposit comprises multiple scheelite ore bodies; multilayer skarn-type scheelite ore bodies are dominant, with a small amount of quartz vein-type ore bodies. Skarn minerals include diopside, hedenbergite, grossular, and epidote. Three mineralization stages exist: skarn, quartz–scheelite, and calcite. The homogenization temperatures of fluid inclusions in hydrothermal minerals that formed in different paragenetic phases were measured as follows: 221–423 °C (early skarn stage), 177–260 °C (quartz–scheelite stage), and 173–227 °C (late calcite stage). The measured salinity of fluid inclusions ranged from 0.18% to 16.34% NaCleqv (skarn stage), 0.35%–7.17% NaCleqv (quartz–scheelite stage), and 0.35%–2.24% NaCleqv (late calcite vein stage). Laser Raman spectroscopic studies on fluid inclusions in the three stages showed H₂O as the main component, with N₂ present in minor amounts. Minor amounts of CH₄ were found in the quartz–scheelite stage. It was observed that the homogenization temperature gradually reduced from the early to the late mineralization stages; moreover, δ¹³C_PDB values for ore-bearing skarn in the mineralization period ranged from ? 5.7‰ to ? 6.9‰ and the corresponding δ¹⁸O_SMOW values ranged from 5.8‰ to 9.1‰, implying that the ore-forming fluid was mainly sourced from magmatic water with a minor amount of meteoric water. Collectively, the evidence indicates that the formation of the Nanyangtian deposit is related to Laojunshan granitic magmatism.     

Geochemistry and zircon U–Pb geochronology of the Pulang complex,Yunnan province,China

The Pulang complex is located tectonically at the southern margin of the Yidun–Zhongdian island arc belt in Yunnan province, China, and is closely related to formation of the Pulang copper deposit, which is the largest copper deposit in Asia. The Pulang complex can be divided into three intrusion stages based on contact relationships and petrological characteristics: (1) a first stage of quartz dioritic porphyry; (2) a second stage of quartz monzonitic porphyry; and (3) a third stage of granodioritic porphyry. The crystallization ages of these intrusion stages were determined by single-zircon U–Pb dating, yielding ages of 221.0 ± 1.0, 211.8 ± 0.5, and 206.3 ± 0.7 Ma for the first, second, and third stages, respectively. These dates, integrated with previous geochronological data and field investigations, indicate that the second-stage quartz monzonitic porphyry has a close spatial and temporal relationship with the large Pulang porphyry copper deposit. These age data, geochemical and Sr–Nd isotopic results suggest that the Pulang complex formed in the Indo-Chinese epoch (257 ～ 205 Ma) by multiphase intrusion of a mixture of mantle- and crust-derived magmas.     

U–Pb geochronology and Pb isotope characteristics of the Chahgaz volcanogenic massive sulphide deposit,southern Iran

The Chahgaz Zn–Pb–Cu volcanogenic massive sulphide (VMS) deposit occurs within a metamorphosed bimodal volcano–sedimentary sequence in the south Sanandaj–Sirjan Zone (SSZ) of southern Iran. This deposit is hosted by rhyodacitic volcaniclastics and is underlain and overlain by rhyodacitic flows, volcaniclastics, and pelites. Peperitic textures between rhyodacite flows and contact pelites indicate that emplacement of the rhyodacite occurred prior to the lithification of the pelites. The rhyodacitic flows are calc-alkaline, and show rare earth and trace elements features characteristic of arc magmatism. Zircons extracted from stratigraphic footwall and hanging-wall rhyodacitic flows of the Chahgaz deposit yield concordant U–Pb ages of 175.7 ± 1.7 and 172.9 ± 1.4 Ma, respectively, and a mean age of 174 ± 1.2 Ma. This time period is interpreted to represent the age of mineralization of the Chahgaz deposit. This Middle Jurassic age is suggested as a major time of VMS mineralization within pull-apart basins formed during Neo-Tethyan oblique subduction-related arc volcano-plutonism in the SSZ. Galena mineral separates from the layered massive sulphide have uniform lead isotope ratios of ²⁰⁶Pb/²⁰⁴Pb?=?18.604–18.617, ²⁰⁷Pb/²⁰⁴Pb?=?15.654–15.667, and ²⁰⁸Pb/²⁰⁴Pb?=?38.736–38.769; they show a model age of 200 Ma, consistent with the derivation of Pb from a Late Triassic, homogeneous upper crustal source.     

Some new data on the genesis of the Linghou Cu–Pb–Zn polymetallic deposit—Based on the study of fluid inclusions and C–H–O–S–Pb isotopes

The Linghou deposit, located near Hangzhou City of Zhejiang Province, eastern China, is a medium-sized polymetallic sulfide deposit associated with granitic intrusion. This deposit is structurally and lithologically controlled and commonly characterized by ore veins or irregular ore lenses. In this deposit, two mineralization events were identified, of which the former produced the Cu–Au–Ag orebodies, while the latter formed Pb–Zn–Cu orebodies. Silicification and calc-silicate (skarn type), phyllic, and carbonate alternation are four principal types of hydrothermal alteration. The early Cu–Au–Ag and late Pb–Zn–Cu mineralizations are characterized by quartz ± sericite + pyrite + chalcopyrite + bornite ± Au–Ag minerals ± magnetite ± molybdenite and calcite + dolomite + sphalerite + pyrite + chalcopyrite + galena, respectively. Calcite clusters and calcite ± quartz vein are formed during the late hydrothermal stage.The NaCl–H₂O–CO₂ system fluid, coexisting with NaCl–H₂O system fluid and showing the similar homogenization temperatures (385 °C and 356 °C, respectively) and different salinities (16.89–21.68 wt.% NaCl eqv. and 7.70–15.53 wt.% NaCl eqv.), suggests that fluid immiscibility occurred during the Cu–Au–Ag mineralization stage and might have given rise to the ore-metal precipitation. The ore-forming fluid of the Pb–Zn–Cu mineralization mainly belongs to the NaCl–H₂O–CO₂ system of high temperature (~ 401 °C) and mid-high salinity (10.79 wt.% NaCl eqv.).Fluids trapped in the quartz-chalcopyrite vein, Cu–Au–Ag ores, Pb–Zn–Cu ores and calcite clusters yielded δ¹⁸O_H2O and δD values varying from 5.54‰ to 13.11‰ and from − 71.8‰ to − 105.1‰, respectively, indicating that magmatic fluids may have played an important role in two mineralization events. The δ¹³C_PDB values of the calcite change from − 2.78‰ to − 4.63‰, indicating that the CO₃^2 − or CO₂ in the ore-forming fluid of the Pb–Zn–Cu mineralization was mainly sourced from the magmatic system, although dissolution of minor marine carbonate may have also occurred during the ore-forming processes. The sulfide minerals have homogeneous lead isotopic compositions with ²⁰⁶Pb/²⁰⁴Pb ranging from 17.958 to 18.587, ²⁰⁷Pb/²⁰⁴Pb ranging from 15.549 to 15.701, and ²⁰⁸Pb/²⁰⁴Pb ranging from 37.976 to 39.052, indicating that metallic elements of the Linghou deposit came from a mixed source involving mantle and crustal components.Based on geological evidence, fluid inclusions, and H–O–C–S–Pb isotopic data, the Linghou polymetallic deposit is interpreted as a high-temperature, skarn-carbonate replacement type. Two types of mineralization are both related to the magmatic–hydrothermal system, with the Cu–Au–Ag mineralization having a close relationship with granodiorite.     

Late Palaeoproterozoic post-collisional magmatism in the North China Craton: geochemistry,zircon U–Pb geochronology,and Hf isotope of the pyroxenite–gabbro–diorite suite from Xinghe,Inner Mongolia

The North China Craton (NCC) witnessed a prolonged subduction–accretion history from the early to late Palaeoproterozoic, culminating with final collision at ca. 1.85 Ga and assembling the continental blocks into the cratonic framework. Subsequently, widespread post-collisional magmatism occurred, particularly along the Trans-North China Orogen (TNCO) that sutures the Eastern and Western blocks of the NCC. Here we present petrological, geochemical, and zircon U–Pb geochronological and Lu–Hf data from a pyroxenite (websterite)–gabbro–diorite suite at Xinghe in Inner Mongolia along the northern segment of the TNCO. The internal structures and high Th/U values of the zircons from the gabbro–diorite suite suggest magmatic crystallization. LA-ICP-MS U–Pb age data on three gabbros and one diorite from the suite yield emplacement ages of 1786.1 ± 4.8, 1783 ± 15 ,1754 ± 16 and 1767 ± 13 Ma, respectively. The ε_Hf(t) shows mostly positive values (up to 5.8), with the lowest value at –4.2, suggesting that the magma was derived from dominantly juvenile sources. The generally low SiO₂ and high MgO values, and other trace element features of the Xinghe suite are consistent with fractionation from a mantle-derived magma with a broadly E-MORB affinity, with no significant crustal contamination. Recent studies clearly establish that the major magmatic pulse associated with rifting of the NCC within the Columbia supercontinent occurred in the late Mesoproterozoic at ca. 1.3–1.2 Ga associated with mantle plume activity. This, together with the lack of robust geochemical imprints of rift-related magmatism in the Xinghe suite, prompts us to suggest a tectonic model that envisages magma genesis associated with post-collisional extension during slab break-off, following the westward subduction of the Eastern Block and its collision with the Western Block. The resulting asthenospheric upwelling and heat input might have triggered the magma generation from a heterogeneous, subduction-modified sub-lithospheric mantle source for the Xinghe rocks, as well as for similar late Palaeoproterozoic suites in the TNCO.     

Ore Deposit Geology and Genesis of the Haobugao Zn–Fe Deposit, Inner Mongolia, NE China

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