Geological and Geochemical Characteristics and Genesis of the Shaxi Porphyry Copper (Gold) Deposits, Anhui Province

The Shaki porphyry copper(gold) deposits are a trpical example of porphyry copper deposits associ-ated with diorite in eastern China. Quartz diorite, which hosts the deposits, has a Rb-Sr isochron age of 127.9±1.6Ma. Geochemically, the rock is rich in alkalis (especially sodium), light rare earth elements (LREE) and large-ionlithophile elements (LILE), and has a relatively low initial strontium isotopic ratio (I_(Sr)=0.7058); thus it is the productof differentiation of crust-mantle mixing source magma. The model of alteration and mineralization zoning is similarto the Hollister (1974) diorite model. The ore fluids have a relatively high salinity and contain significant amounts ofCO_2, Ca~(2+), Na~+ and Cl~-. The homogenization temperatures of fluid inclusions for the main mineralization stage rangefrom 280 to 420℃, the δ~(18)O values of the ore fluids vary from 3.51 to 5.52‰, the δD values are in the range between-82.4 and -59.8‰, the δ~(34)S values of sulphides vary from -0.3 to 2.49‰, and the δ~(13)C values of CO_2 in inclusionsrange between -2.66 and -6.53‰. Isotope data indicate that the hydrothermal ore fluids and ore substances of theShaxi porphyry copper (gold) deposits were mainly derived from magmatic systems.     

Geology and Isotope Geochemistry of the Yinchanggou-Qiluogou Pb-Zn Deposit, Sichuan Province, Southwest China

The Yinchanggou-Qiluogou Pb-Zn deposit,located in the western Yangtze Block,southwest China,is hosted by the Upper Sinian Dengying Formation dolostone.Ore bodies occur in the Qiluogou anticline and the NS-and NNW-trending faults.Sulfide ores mainly consist of sphalerite,pyrite,galena and calcite,with subordinate dolomite and quartz.Seventeen ore bodies have been discovered to date and they have a combined 1.0 million tons of sulfide ores with average grades of 2.27wt%Zn and 6.89wt%Pb.The δD_(H2O-SMOW) and δ~(18)O_(H2O-SMOW) values of fluid inclusions in quartz and calcite samples range from-68.9‰ to-48.7‰ and 7.3‰ to 15.9‰,respectively,suggesting that H_2O in the hydrothermal fluids sourced from metamorphic water.Calcite samples have δ~(13)C_(PDB) values ranging from-6.2‰ to-4.1‰ and δ~(18)O_(SMOW) values ranging from 15.1‰ to 17.4‰,indicating C and O in the hydrothermal fluids likely derived from a mixed source of metamorphic fluids and the host carbonates.The δ~(34)S_(CDT) values of sulfide minerals range from 5.5‰ to 20.3‰,suggesting that thermal chemical reduction of sulfate minerals in evaporates were the most probable source of S in the hydrothermal fluids.The ~(206)Pb/~(204)Pb,~(207)Pb/~(204)Pb and ~(208)Pb/~(204)Pb ratios of sulfide minerals fall in the range of 18.11 to 18.40,15.66 to 15.76 and 38.25 to 38.88,respectively.The Pb isotopic data of the studied deposit plot near the upper crust Pb evolution curve and overlap with the age-corrected Proterozoic basement rocks and the Upper Sinian Dengying Formation hosting dolostone.This indicates that the Pb originated from a mixed source of the basement metamorphic rocks and the ore-hosting carbonate rocks.The ore geology and C-H-O-S-Pb isotopic data suggest that the YinchanggouQiluogou deposit is an unusual carbonate-hosted,strata-bound and epigenetic deposit that derived ore-forming materials from a mixed source of the underlying Porterozoic basements and the Sinian hosting carbonates.     

Genesis of the Gold Deposit in the Indus-Yarlung Tsangpo Suture Zone, Southern Tibet: Evidence from Geological and Geochemical Data

The Nianzha gold deposit,located in the central section of the Indus-Yarlung Tsangpo suture(IYS) zone in southern Tibet,is a large gold deposit(Au reserves of 25 tons with average grade of 3.08 g/t) controlled by a E-W striking fault that developed during the main stage of Indo-Asian collision(~65-41 Ma).The main orebody is 1760 m long and 5.15 m thick,and occurs in a fracture zone bordered by Cretaceous diorite in the hanging wall to the north and the Renbu tectonic melange in the footwall to the south.High-grade mineralization occurs in a fracture zone between diorite and ultramafic rock in the Renbu tectonic melange.The wall-rock alteration is characterized by silicification in the fracture zone,serpentinization and the formation of talc and magnesite in the ultramafic unit,and chloritization and the formation of epidote and calcite in diorite.Quartz veins associated with Au mineralization can be divided into three stages.Fluid inclusion data indicate that the deposit formed from H_2O-NaCl-organic gas fluids that homogenize at temperatures of 203℃-347℃ and have salinities of 0.35wt%-17.17wt%NaCl equivalent.The quartz veins yield δ~(18)O_(fluid) values of 0.15‰-10.45‰,low δD_(V-SMOW)values(-173‰ to-96‰),and the δ~(13)C values of-17.6‰ to-4.7‰,indicating the ore-forming fluids were a mix of metamorphic and sedimentary orogenic fluids with the addition of some meteoric and mantle-derived fluids.The pyrite within the diorite has δ~(34)S_(V-CDT) values of-2.9‰-1.9‰(average-1.1‰),~(206)Pb/~(204)Pb values of 18.47-18.64,~(207)Pb/~(204)Pb values of 15.64-15.74,and ~(208)Pb/~(204)Pb values of 38.71-39.27,all of which are indicative of the derivation of S and other ore-forming elements from deep in the mantle.The presence of the Nianzha,Bangbu,and Mayum gold deposits within the IYS zone indicates that this area is highly prospective for large orogenic gold deposits.We identified three types of mineralization within the IYS,namely Bangbu-type accretionary,Mayum-type microcontinent,and Nianzha-type ophiolite-associated orogenic Au deposits.The three types formed at different depths in an accretionary orogenic tectonic setting.The Bangbu type was formed at the deepest level and the Nianzha type at the shallowest.     

Genesis of the Dalingzi Pb-Zn Deposit in the Western Margin of Yangtze Plate: Constraints from Fluid Inclusions and Isotopic EvidenceEI北大核心CSCD

The Daliangzi Pb-Zn deposit is a large deposit hosted in the Sinian Dengying Formation dolostone, located in the Sichuan-Yunnan-Guizhou ore concentration area. Ore minerals are mianly sphalerite, galena, and gangue minerals consist of dolomite, quartz and calcite. The metallogenic stages may be divided into sphalerite-pyrite-carbon stage, sphalerite-galena stage and galena-chalcopyrite-carbonate stage. The ore-forming fluid is basin brine, which is characterized by medium-low temperature of 117.5 ℃ to 320.3 ℃ and medium salinity of 5.11% NaCleqv to 18.96% NaCleqv, moreover, the abundant CH4 and pitch in the fluid inclusions indicate that the participation of organic matter in the mineralization. The δ13CV-PDB and δ18OSMOW values of the Dengying Formation dolostone are similar to that of marine carbonate, revealing that the dolostone belongs to marine carbonate. Both the δ13CV-PDB and δ18OSMOW values of hydrothermal calcites are lower than that of the Dengying Formation dolostone, which may result from dissolution of the Dengying Formation dolostone. The δ34S values of ore minerals are mainly in the range of 9.8‰-20.8‰, indicating the sulfur may come from thermochemical reduction of marine sulfate in the Dengying Formation. The 207Pb/204Pb versus 206Pb/204Pb diagram manifests that Pb is crustal origin, and likely comes mainly from the wall rocks and less from the basement. (87Sr/86Sr)i ratios of sphalerites and hydrothermal calcite are higher than that of the Dengying Formation dolostone, indicating that the ore-forming fluid flew through the basement. In conclusion, the ore-forming fluid was basin brine, which extracted the metallogenic materials, Pb and Zn, from the basement and wall rocks. When the ore-forming fluid reached the "black fractured zones", carbonized tectonic breccia zone, S2- was produced by the thermochemical reduction reaction under the influence of the organic matter, and interaction between the S2- and Pb2+, Zn2+, resulted in the precipitation of ore metals. © 2018, Science Press. All right reserved.     

Genesis of the Changba–Lijiagou Giant Pb-Zn Deposit, West Qinling, Central China: Constraints from S-Pb-C-O isotopes

The extensive Changba-Lijiagou Pb-Zn deposit is located in the north of the Xihe–Chengxian ore cluster in West Qinling. The ore bodies are mainly hosted in the marble, dolomitic marble and biotite-calcite-quartz schist of the Middle Devonian Anjiacha Formation, and are structurally controlled by the fault and anticline. The ore-forming process can be divided into three main stages, based on field geological features and mineral assemblages. The mineral assemblages of hydrothermal stage I are pale-yellow coarse grain, low Fe sphalerite, pyrite with pits, barite and biotite. The mineral assemblages of hydrothermal stage II are black-brown cryptocrystalline, high Fe shalerite, pyrite without pits, marcasite or arsenopyrite replace the pyrite with pits, K-feldspar. The features of hydrothermal stage III are calcite-quartz-sulfide vein cutting the laminated, banded ore body. Forty-two sulfur isotope analyses, twenty-five lead isotope analyses and nineteen carbon and oxygen isotope analyses were determined on sphalerite, pyrite, galena and calcite. The δ34 S values of stage I(20.3 to 29.0‰) are consistent with the δ34 S of sulfate(barite) in the stratum. Combined with geological feature, inclusion characteristics and EPMA data, we propose that TSR has played a key role in the formation of the sulfides in stage I. The δ34 S values of stage II sphalerite and pyrite(15.1 to 23.0‰) are between sulfides in the host rock, magmatic sulfur and the sulfate(barite) in the stratum. This result suggests that multiple S reservoirs were the sources for S2-in stage II. The δ34 S values of stage III(13.1 to 22‰) combined with the structure of the geological and mineral features suggest a magmatic hydrothermal origin of the mineralization. The lead isotope compositions of the sulfides have 206 Pb/204 Pb ranging from 17.9480 to 17.9782, 207 Pb/204 Pb ranging from 15.611 to 15.622, and 208 Pb/204 Pb ranging from 38.1368 to 38.1691 in the three ore-forming stages. The narrow and symmetric distributions of the lead isotope values reflect homogenization of granite and mantle sources before the Pb-Zn mineralization. The δ13 CPDB and δ18 OSMOW values of stage I range from-0.1 to 2.4‰ and from 18.8 to 21.7‰. The values and inclusion data indicate that the source of fluids in stage I was the dissolution of marine carbonate. The δ13 CPDB and δ18 OSMOW values of stage II range from-4 to 1‰ and from 12.3 to 20.3‰, suggesting multiple C-O reservoirs in the Changba deposit and the addition of mantle-source fluid to the system. The values in stage III are-3.1‰ and 19.7‰, respectively. We infer that the process of mineralization involved evaporitic salt and sedimentary organic-bearing units interacting through thermochemical sulfate reduction through the isotopic, mineralogy and inclusion evidences. Subsequently, the geology feature, mineral assemblages, EPMA data and isotopic values support the conclusion that the ore-forming hydrothermal fluids were mixed with magmatic hydrothermal fluids and forming the massive dark sphalerite, then yielding the calcite-quartz-sulfide vein ore type at the last stage. The genesis of this ore deposit was epigenetic rather than the previously-proposed sedimentary-exhalative(SEDEX) type.     

Genesis of the Bangbu Orogenic Gold Deposit,Tibet: Evidence from Fluid Inclusion,Stable Isotopes,and Ar-Ar Geochronology

The Bangbu gold deposit is a large orogenic gold deposit in Tibet formed during the AlpineHimalayan collision. Ore bodies(auriferous quartz veins) are controlled by the E-W-trending Qusong-Cuogu-Zhemulang brittle-ductile shear zone. Quartz veins at the deposit can be divided into three types: pre-metallogenic hook-like quartz veins, metallogenic auriferous quartz veins, and postmetallogenic N-S quartz veins. Four stages of mineralization in the auriferous quartz veins have been identified:(1) Stage S1 quartz+coarse-grained sulfides,(2) Stage S2 gold+fine-grained sulfides,(3) Stage S3 quartz+carbonates, and(4) Stage S4 quartz+ greigite. Fluid inclusions indicate the oreforming fluid was CO_2-N_2-CH_4 rich with homogenization temperatures of 170–261°C, salinities 4.34–7.45 wt% Na Cl equivalent. δ~(18)Ofluid(3.98‰–7.18‰) and low δDV-SMOW(-90‰ to-44‰) for auriferous quartz veins suggest ore-forming fluids were mainly metamorphic in origin, with some addition of organic matter. Quartz vein pyrite has δ~(34)SV-CDT values of 1.2‰–3.6‰(an average of 2.2‰), whereas pyrite from phyllite has δ~(34)SV-CDT 5.7‰–9.9‰(an average of 7.4‰). Quartz vein pyrites yield 206Pb/204 Pb ratios of 18.662–18.764, 207Pb/204 Pb 15.650–15.683, and ~(208)Pb/204 Pb 38.901–39.079. These isotopic data indicate Bangbu ore-forming materials were probably derived from the Langjiexue accretionary wedge. 40Ar/39 Ar ages for sericite from auriferous sulfide-quartz veins yield a plateau age of 49.52 ± 0.52 Ma, an isochron age of 50.3 ± 0.31 Ma, suggesting that auriferous veins were formed during the main collisional period of the Tibet-Himalayan orogen(~65–41 Ma).     

S and Pb Isotopic Constraints on the Relationship between the Linong Granodiorite and the Yangla Copper Deposit,Yunnan, China

The Yangla copper deposit, located in western Yunnan Province, China, is a typical giant, newly started mining copper deposit with an estimated Cu reserves of about 1,200,000 tons. The deposit is spatially and temporally associated with the Linong granodiorite, which is rich in SiO2 (SiO2=58.25 wt%–69.84 wt%) and alkalis (Na2O+K2O=5.98 wt%–8.34 wt%), indicating an association with shoshonitic series to high-K calc-alkaline series granites, and shows low contents of TiO2 (0.35 wt%–0.48 wt%), MgO (1.51 wt%–1.72 wt%), and Al2O3 (13.38 wt%–19.75 wt%). The δ34S values of sulfides of the main ore stage from copper ores vary range from ?4.2‰ to ?0.9‰, indicating a much greater contribution from the mantle to the ore-forming fluids. The δ34S values of the late ore stage is ?9.8‰, indicating enrichment of biogenic sulfur which may derive from the crustal hydrothermal fluid. The 208Pb/204Pb, 207Pb/204Pb and 206Pb/204Pb of sulfides of the main ore stage from copper ores range within 38.66–38.73, 15.71–15.74 and 18.35–19.04, respectively, implying that the Pb was derived from the mantle, with the crustal component, probably representing mixtures of mantle lead and crustal lead. Sulfide of the late ore stage in their Pb isotopic composition, 208Pb/204Pb= 38.69, 207Pb/204Pb=15.70, 206Pb/204Pb=18.35, implying that the Pb was derived from the crust. The Linong granodiorite is syn-collisional, produced by partial melting of thickened lower crust, which was triggered by the westward subduction of the Jinshajiang Oceanic plate. During a transition in geodynamic setting from collision-related compression to extension, gently dipping ductile shear zones (related to subduction) were transformed to brittle shear zones, consisting of a series of thrust faults in the Jinshajiang tectonic belt. The tensional thrust faults would have been a favorable environment for ore-forming fluids. The ascending magma provided a channel for the ore-forming fluid from the mantle wedge. After the magma arrived at the base of the early-stage Linong granodiorite, the platy granodiorite at the base of the body would have shielded the late-stage magma from the fluid. The magma would have cooled slowly, and some of the ore-forming fluid in the magma would have entered the gently dipping thrust faults near the Linong granodiorite, resulting in mineralization.     

H-O-S-Pb Isotopic Compositions of the Chagele Pb-Zn-Cu-Mo Deposit,Tibet: Implications for the Ore-forming Processes and Comparison with Pb-Zn (Cu-Mo) Deposits in Middle-east Segment of the Nyainqentanglha Metallogenic BeltEI北大核心CSCD

The Chagele is a typical Pb-Zn-Cu-Mo deposit located in the western Nyainqentanglha Pb-Zn-Ag-Fe-Cu metallogenic belt (NPMB) that immediately north of the Gangdese porphyry copper belt, Tibet. The deposit contains three ore types: the porphyry (Cu) Mo ores occur as thin veins hosted in the granite porphyry; the skarn (Cu) Pb-Zn type ores are of vein-type or lenticular-type mainly occurring in the external contact zone and interstratified crack zone; and the hydrothermal vein Pb-Zn type ores are controlled by the NNE-striking faults and situated in the structural fractured zones and the up walls of fault zones. The (Cu) Pb-Zn ores consist mainly of galena, sphalerite, chalcopyrite, pyrite, malachite, showing automorphic granular, hypautomorphic to allotriomorphic granular and metasomatic-relict textures, and exhibiting mainly veined, banded, disseminated and massive structures. Hydrothermal alteration includes skarnization, silicification and limonitization. The (Cu) Mo ores consists mainly of chalcopyrite and molybdenite, and minor pyrite. The (Cu) Mo ores are characterized by scaly texture, veinlet and massive structures. It has reserves of 0.38 Mt Pb, 0.6 Mt Zn and 110.1 t Ag, with average grade of 2.08%, 3.29% and 6.07 g/t, respectively, and is considered as a deposit with huge ore-prospecting potential in western of NPMB. However, the ore-forming material and genesis of the Chagele deposit are still not clear. This paper systematically investigated the H, O, S and Pb isotopes of the Chagele deposit and compared it with the other Pb-Zn (Cu-Mo) deposits in the middle-east segment of NPMB. Isotopic geochemical analyses showed that the fluids have δ18O values of -2.2‰ to 2.9‰ and δD values of -189‰ to -157‰, respectively, indicative of mixing between magmatic and meteoric waters. The bimodal distribution of δ34 S values for sulfides (-5.6‰ to -0.8‰, the average: -3.7‰ and 1.1‰ to 2.6‰, the average: 1.8‰) indicated that sulfur of the ores were derived from both wall rocks and magma, while the Cu-Mo orebodies was mainly derived from the granite porphyry. The sulfides have 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb values in ranges of 18.614 to 18.688, 15.657 to 15.747 and 38.988 to 39.269; similarly the granite porphyries have 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb values of 18.663 to 19.058, 15.643 to 15.664, and 39.002 to 39.559, respectively, implying that both of them were originated from the upper crust. The H-O-S-Pb isotopic characteristics of the Chagele deposit are similar to those of the Pb-Zn polymetallic deposits in the mid-east NPMB, suggesting that these deposits have similar ore-forming fluid and material sources. It can be concluded that the Chagele deposit is a typical porphyry type Mo deposit + skarn type-hydrothermal vein type of Cu-Pb-Zn deposit. Moreover, we argue that the mineralization is not only confined to the mid-east NPMB, the western segment of the belt with similar tectonic-magmatism also has high potential of ore mineralization. © 2018, Science Press. All right reserved.     

Geological Characteristics and Genesis of the Jiamoshan MVT Pb–Zn Deposit in the Sanjiang belt, Tibetan Plateau

The carbonate-hosted Pb–Zn deposits in the Sanjiang metallogenic belt on the Tibetan Plateau are typical of MVT Pb–Zn deposits that form in thrust-fold belts. The Jiamoshan Pb–Zn deposit is located in the Changdu area in the middle part of the Sanjiang belt, and it represents a new style of MVT deposit that was controlled by karst structures in a thrust–fold system. Such a karst-controlled MVT Pb–Zn deposit in thrust settings has not previously been described in detail, and we therefore mapped the geology of the deposit and undertook a detailed study of its genesis. The karst structures that host the Jiamoshan deposit were formed in Triassic limestones along secondary reverse faults, and the orebodies have irregular tubular shapes. The main sulfide minerals are galena, sphalerite, and pyrite that occur in massive and lamellar form. The ore-forming fluids belonged to a Mg2+–Na+–K+–SO2-4–Cl-–F-–NO-3–H2 O system at low temperatures(120–130°C) but with high salinities(19–22% NaCl eq.). We have recognized basinal brine as the source of the ore-forming fluids on the basis of their H–O isotopic compositions(-145‰ to-93‰ for δDV-SMOW and-2.22‰ to 13.00‰ for δ18 Ofluid), the ratios of Cl/Br(14–1196) and Na/Br(16–586) in the hydrothermal fluids, and the C–O isotopic compositions of calcite(-5.0‰ to 3.7‰ for δ13 CV-PDB and 15.1‰ to 22.3‰ for δ18 OV-SMOW). These fluids may have been derived from evaporated seawater trapped in marine strata at depth or from Paleogene–Neogene basins on the surface. The δ34 S values are low in the galena(-3.2‰ to 0.6‰) but high in the barite(27.1‰), indicating that the reduced sulfur came from gypsum in the regional Cenozoic basins and from sulfates in trapped paleo-seawater by bacterial sulfate reduction. The Pb isotopic compositions of the galena samples(18.3270–18.3482 for 206 Pb/204 Pb, 15.6345–15.6390 for 207 Pb/204 Pb, and 38.5503–38.5582 for 208 Pb/204 Pb) are similar to those of the regional Triassic volcanic-arc rocks that formed during the closure of the Paleo-Tethys, indicating these arc rocks were the source of the metals in the deposit. Taking into account our new observations and data, as well as regional Pb–Zn metallogenic processes, we present here a new model for MVT deposits controlled by karst structures in thrust–fold systems.     

Geochemical Characteristics and Sources of Ore-forming Fluids of the Mayuan Pb-Zn Deposit, Nanzheng, Shaanxi, China

The Mayuan stratabound Pb-Zn deposit in Nanzheng,Shaanxi Province,is located in the northern margin of the Yangtze Plate,in the southern margin of the Beiba Arch.The orebodies are stratiform and hosted in breciated dolostone of the Sinian Dengying Formation.The ore minerals are primarily sphalerite and galena,and the gangue minerals comprise of dolomite,quartz,barite,calcite and solid bitumen.Fluid inclusions from ore-stage quartz and calcite have homogenization tempreatures from 98 to 337℃ and salinities from 7.7 wt%to 22.2 wt%(NaCl equiv.).The vapor phase of the inclusions is mainly composed of CH_4 with minor CO_2 and H_2S.The δD_(fluid) values of fluid inclusions in quartz and calcite display a range from-68‰ to-113‰(SMOW),and the δ~(18)O_(fluid)values calculated from δ~(18)O_(quartz) and δ~(18)O_(calcite) values range from 4.5‰ to 16.7‰(SMOW).These data suggest that the ore-forming fluids may have been derived from evaporitic sea water that had reacted with organic matter.The δ~(13)C_(CH4) values of CH_4 in fluid inclusions range from-37.2‰ to-21.0‰(PDB),suggesting that the CH_4 in the ore-forming fluids was mainly derived from organic matter.This,together with the abundance of solid bitumen in the ores,suggest that organic matter played an important role in mineralization,and that the thermochemical sulfate reduction(TSR) was the main mechanism of sulfide precipitation.The Mayuan Pb-Zn deposit is a carbonate-hosted epigenetic deposit that may be classified as a Mississippi Valley type(MVT) deposit.     

Genesis of the Xiuwenghala Gold Deposit in the Beishan Orogen,Northwest China: Evidence from Geology,Fluid Inclusion,and H–O–S–Pb Isotopes

The Xiuwenghala gold deposit is located in the Beishan Orogen of the southern Central Asian Orogenic Belt. The vein/lenticular gold orebodies are controlled by Northeast‐trending faults and are hosted mainly in the brecciated/altered tuff and rhyolite porphyry of the Lower Carboniferous Baishan Formation. Metallic minerals include mainly pyrite and minor chalcopyrite, arsenopyrite, galena, and sphalerite, whilst nonmetallic minerals include quartz, chalcedony, sericite, chlorite, and calcite. Hydrothermal alterations consist of silicic, sericite, chlorite, and carbonate. Alteration/mineralization processes comprise three stages: pre‐ore silicic alteration (Stage I), syn‐ore quartz‐chalcedony‐polymetallic sulfide mineralization (Stage II), and post‐ore quartz‐calcite veining (Stage III). Fluid inclusions (FIs) in quartz and calcite are dominated by L‐type with minor V‐type and lack any daughter mineral‐bearing or CO₂‐rich/‐bearing inclusions. From Stages I to III, the FIs homogenized at 240–260°C, 220–250°C, and 150–190°C, with corresponding salinities of 2.9–10.9, 3.2–11.1, and 2.9–11.9 wt.% NaCl eqv., respectively. The mineralization depth at Xiuwenghala is estimated to be relatively shallow (<1 km). FI results indicate that the ore‐forming fluids belong to a low to medium‐temperature, low‐salinity, and low‐density NaCl‐H₂O system. The values decrease from Stage I to III (3.7‰, 1.7–2.4‰, and ?1.7 to 0.9‰, respectively), and a similar trend is found for their values (?104 to ?90‰, ?126 to ?86‰, and ?130 to ?106‰, respectively). This indicates that the fluid source gradually evolved from magmatic to meteoric. δ³⁴S values of the hydrothermal pyrites (?3.0 to 0.0‰; avg. ?1.1‰) resemble those of typical magmatic/mantle‐derived sulfides. Pyrite Pb isotopic compositions (²⁰⁶Pb/²⁰⁴Pb = 18.409–18.767, ²⁰⁷Pb/²⁰⁴Pb = 15.600–15.715, ²⁰⁸Pb^/204Pb = 38.173–38.654) are similar to those of the (sub)volcanic ore host, indicating that the origin of ore‐forming material was mainly the upper crustal (sub)volcanic rocks. Integrating evidence from geology, FIs, and H–O–S–Pb isotopes, we suggest that Xiuwenghala is best classified as a low‐sulfidation epithermal gold deposit.     

Genesis of Pb–Zn Mineralization Beneath the Xiangshan Uranium Orefield,South China: Constraints from H–O–S–Pb Isotopes and Rb–Sr Dating

The volcanic‐hosted Xiangshan uranium orefield is the largest uranium deposit in South China. Recent exploration has discovered extensive Pb–Zn mineralization beneath the uranium orebodies. Detailed geological investigation reveals that the major metallic minerals include pyrite, sphalerite, galena, and chalcopyrite, whilst the major non‐metallic minerals include quartz, sericite, and calcite. New δ¹⁸O_fluid and δD_fluid data indicate that the ore‐forming fluids were mainly derived from magmatic, and the sulfide δ³⁴S values (2.2–6.9‰) suggest a dominantly magmatic sulfur source. The Pb isotope compositions are homogeneous (²⁰⁶Pb/²⁰⁴Pb = 18.120–18.233, ²⁰⁷Pb/²⁰⁴Pb = 15.575–15.698, and ²⁰⁸Pb/²⁰⁴Pb = 37.047–38.446). The ⁸⁷Sr/⁸⁶Sr ratios of sulfide minerals range from 0.7197 to 0.7204, which is much higher than volcanic rocks and fall into the range of metamorphic basement. Lead and strontium isotopic compositions indicate that the metallogenic materials probably were derived from metamorphic basement. Pyrite Rb–Sr dating of the ores yielded 131.3 ± 4.0 Ma, indicating that the Pb–Zn mineralization occurred in the Early Cretaceous.     

Geochronology and Genesis of the Tiegelongnan Porphyry Cu(Au) Deposit in Tibet: Evidence from U–Pb,Re–Os Dating and Hf,S, and H–O Isotopes

The Tiegelongnan Cu (Au) deposit is the largest copper deposit newly discovered in the Bangong–Nujiang metallogenic belt. The deposit has a clear alteration zoning consisting of, from core to margin, potassic to propylitic, superimposed by phyllic and advanced argillic alteration. The shallow part of the deposit consists of a high sulphidation‐state overprint, mainly comprising disseminated pyrite and Cu–S minerals such as bornite, covellite, digenite, and enargite. At depth porphyry‐type mineralization mainly comprises disseminated chalcopyrite, bornite, pyrite, and a minor vein molybdenite. Mineralization is disseminated and associated with veins contained within the porphyry intrusions and their surrounding rocks. The zircon U–Pb ages of the mineralized diorite porphyry and granodiorite porphyry are 123.1 ± 1.7 Ma (2σ) and 121.5 ± 1.5 Ma (2σ), respectively. The molybdenite Re–Os age is 121.2 ± 1.2 Ma, suggesting that mineralization was closely associated with magmatism. Andesite lava (zircon U–Pb age of 111.7 ± 1.6 Ma, 2σ) overlies the ore‐bodies and is the product of post‐mineralization volcanic activity that played a critical role in preserving the ore‐bodies. Values of ?4.6 ‰ to + 0.8 ‰ δ³⁴S for the metal sulfides (mean ? 1.55 ‰) suggest that S mainly has a deep magmatic source. The H and O isotopic composition is (δD = ?87 ‰ to ?64 ‰; δ¹⁸O_H2O = 5.5 ‰ to 9.0 ‰), indicating that the ore‐forming fluids are mostly magmatic‐hydrothermal, possibly mixed with a small amount of meteoric water. The zircon ε_Hf(t) of the diorite porphyry is 3.7 to 8.3, and the granodiorite porphyry is 1.8 to 7.5. Molybdenite has a high Re from 382.2 × 10^?6 to 1600 × 10^?6. Re and Hf isotope composition show that Tiegelongnan has some mantle source, maybe the juvenile lower crust from crust–mantle mixed source. Metallogenesis of the Tiegelongnan giant porphyry system was associated with intermediate to acidic magma in the Early Cretaceous (~120 Ma). The magma provenance of the Tiegelongnan deposit has some mantle‐derived composition, possibly mixed with the crust‐derived materials.     

Geology and Isotope Geochemistry of the Dongzhongla Pb–Zn Deposit in Tibet: Implications for the Origin of the Ore‐Forming Fluids and Storage Condition of Certain Metals

As a newly discovered medium‐sized deposit (proven Pb + Zn resources of 0.23 Mt, 9.43% Pb and 8.73% Zn), the Dongzhongla skarn Pb–Zn deposit is located in the northern margin of the eastern Gangdese, central Lhasa block. Based on the geological conditions in this deposit of ore‐forming fluids, H, O, C, S, Pb, Sr, and noble gas isotopic compositions were analyzed. Results show that δ¹⁸O_SMOW of quartz and calcite ranged from −9.85 to 4.17‰, and δD_SMOW ranged from −124.7 to −99.6‰ (where SMOW is the standard mean ocean water), indicating magma fluids mixed with meteoric water in ore‐forming fluids. The δ¹³C_PDB and δ¹⁸O_SMOW values of calcite range from −1.4 to −1.1‰ and from 5.3 to 15.90‰, respectively, show compositions consistent with the carbonate limestone in the surrounding rocks, implying that the carbon was primarily sourced from the dissolution of carbonate strata in the Luobadui Formation. The ore δ³⁴S composition varied in a narrow range of 2.8 to 5.7‰, mostly between 4‰ and 5‰. The total sulfur isotopic value δ³⁴S was 4.7‰ with characteristics of magmatic sulfur. The ³He/⁴He values of pyrite and galena ranged from 0.101 to 5.7 Ra, lower than those of mantle‐derived fluids (6 ± 1 Ra), but higher than those of the crust (0.01–0.05 Ra), and therefore classified as a crust–mantle mixed source. The Pb isotopic composition for ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb, and ²⁰⁸Pb/²⁰⁴Pb values of the ores were in the ranges of 18.628–18.746, 15.698–15.802, and 39.077–39.430, respectively, consistent with the Pb isotopic composition of magmatic rocks in the deposit, classified as upper‐crust lead. The ore lead was likely sourced partially from the crustal basement of the Lhasa Terrane. The initial (⁸⁷Sr/⁸⁶Sr)_i value from five sulfide samples ranged from 0.71732 to 0.72767, and associated ore‐forming fluids were mainly sourced from the partial melting of the upper‐crust materials. Pb isotopic compositions of ore sulfides from the Dongzhongla deposit are similar to that of the Yuiguila and Mengya'a deposit, indicating that they have similar sources of metal‐rich ore‐forming solution. According to basic skarn mineralogy, the economic metals, and the origin of the ore‐forming fluids, the Dongzhongla deposit was classified as a skarn‐type Pb–Zn deposit.     

Two Periods of Skarn Mineralization in the Baizhangyan W–Mo Deposit,Southern Anhui Province,Southeast China: Evidence from Zircon U–Pb and Molybdenite Re–Os and Sulfur Isotope Data

The recently discovered Baizhangyan skarn‐porphyry type W–Mo deposit in southern Anhui Province in SE China occurs near the Middle–Lower Yangtze Valley polymetallic metallogenic belt. The deposit is closely temporally‐spatially associated with the Mesozoic Qingyang granitic complex composed of g ranodiorite, monzonitic g ranite, and alkaline g ranite. Orebodies of the deposit occur as horizons, veins, and lenses within the limestones of Sinian Lantian Formation contacting with buried fine‐grained granite, and diorite dykes. There are two types of W mineralization: major skarn W–Mo mineralization and minor granite‐hosted disseminated Mo mineralization. Among skarn mineralization, mineral assemblages and cross‐cutting relationships within both skarn ores and intrusions reveal two distinct periods of mineralization, i.e. the first W–Au period related to the intrusion of diorite dykes, and the subsequent W–Mo period related to the intrusion of the fine‐grained granite. In this paper, we report new zircon U–Pb and molybdenite Re–Os ages with the aim of constraining the relationships among the monzonitic granite, fine‐grained granite, diorite dykes, and W mineralization. Zircons of the monzonitic granite, the fine‐grained granite, and diorite dykes yield weighted mean U–Pb ages of 129.0 ± 1.2 Ma, 135.34 ± 0.92 Ma and 145.3 ± 1.7 Ma, respectively. Ten molybdenite Re–Os age determinations yield an isochron age of 136.9 ± 4.5 Ma and a weighted mean age of 135.0 ± 1.2 Ma. The molybdenites have δ³⁴S values of 3.6‰–6.6‰ and their Re contents ranging from 7.23 ppm to 15.23 ppm. A second group of two molybdenite samples yield ages of 143.8 ± 2.1 and 146.3 ± 2.0 Ma, containing Re concentrations of 50.5–50.9 ppm, and with δ³⁴S values of 1.6‰–4.8‰. The molybdenites from these two distinct groups of samples contain moderate concentrations of Re (7.23–50.48 ppm), suggesting that metals within the deposit have a mixed crust–mantle provenance. Field observation and new age and isotope data obtained in this study indicate that the first diorite dyke‐related skarn W–Au mineralization took place in the Early Cretaceous peaking at 143.0–146.3 Ma, and was associated with a mixed crust–mantle system. The second fine‐grained granite‐related skarn W–Mo mineralization took place a little later at 135.0–136.9 Ma, and was crust‐dominated. The fine‐grained granite was not formed by fractionation of the Qingyang monzonitic granite. This finding suggests that the first period of skarn W–Au mineralization in the Baizhangyan deposit resulted from interaction between basaltic magmas derived from the upper lithospheric mantle and crustal material at 143.0–146.3 and the subsequent period of W–Mo mineralization derived from the crust at 135.0–136.9 Ma.     

Ore Genesis of the Lunwei Granite‐Related Scheelite Deposit in the Wuyi Metallogenic Belt,Southeast China: Constraints from Geochronology,Fluid Inclusions,and H–O–S Isotopes

A granite‐related scheelite deposit has been recently discovered in the Wuyi metallogenic belt of southeast China. The veinlet–disseminated scheelite occurs mainly in the inner and outer contact zones of the porphyritic biotite granite, spatially associated with potassic feldspathization and silicification. Re–Os dating of molybdenite intergrowths with scheelite yield a well‐constrained isochron age of 170.4 ± 1.2 Ma, coeval with the LA–MC–ICP–MS concordant zircon age of porphyritic biotite granite (167.6 ± 2.2 Ma), indicating that the Lunwei W deposit was formed in the Middle Jurassic (~170 Ma). We identify three stages of ore formation (from early to late): (I) the quartz–K‐feldspar–scheelite stage; (II) the quartz–polymetallic sulfide stage; and (III) the quartz–carbonate stage. Based on petrographic observations and microthermometric criteria, the fluid inclusions in the scheelite and quartz are determined to be mainly aqueous two‐phase (liquid‐rich and gas‐rich) fluid inclusions, with minor gas‐pure and CO₂‐bearing fluid inclusions. Ore‐forming fluids in the Lunwei W deposit show a successive decrease in temperature and salinity from Stage I to Stage III. The homogenization temperature decreases from an average of 299 °C in Stage I, through 251 °C in Stage II, to 212 °C in Stage III, with a corresponding change in salinity from an average of 5.8 wt.%, through 5.2 wt.%, to 3.4 wt.%. The ore‐forming fluids have intermediate to low temperatures and low salinities, belonging to the H₂O–NaCl ± CO₂ system. The δ¹⁸O_H2O values vary from 1.8‰ to 3.3‰, and the δD_V‐SMOW values vary from –66‰ to –76‰, suggesting that the ore‐forming fluid was primarily of magmatic water mixed with various amounts of meteoric water. Sulfur isotope compositions of sulfides (δ³⁴S ranging from –1.1‰ to +2.4‰) and Re contents in molybdenite (1.45–19.25 µg/g, mean of 8.97 µg/g) indicate that the ore‐forming materials originated mainly in the crust. The primary mechanism for mineral deposition in the Lunwei W deposit was a decrease in temperature and the mixing of magmatic and meteoric water. The Lunwei deposit can be classified as a porphyry‐type scheelite deposit and is a product of widespread tungsten mineralization in South China. We summarize the geological characteristics of typical W deposits (the Xingluokeng, Shangfang, and Lunwei deposits) in the Wuyi metallogenic belt and suggest that porphyry and skarn scheelite deposits should be considered the principal exploration targets in this area.     

Geochemistry,zircon U–Pb and molybdenite Re–Os dating of the Taolaituo porphyry Mo deposit in the Central Great Hinggan Range: implications for the geodynamic evolution of northeastern China

The Taolaituo porphyry‐type molybdenum deposit is located in the eastern Inner Mongolia Autonomous Region in China. The mineralization occurs mainly as veins, lenses and layers within the host porphyry. To better understand the link between the mineralization and the host igneous rocks, we studied samples from the underground workings and report new SHRIMP II zircon U–Pb and Re–Os molybdenite ages, and geochemical data from both the molybdenites and the porphyry granites. Five molybdenite samples yield a Re–Os isochron weighted mean age of 133.0 ± 0.82 Ma, whereas the porphyry granitoids samples yield crystallization ages of 133 ± 1 Ma and 130.4 ± 1.3 Ma. The U–Pb and Re–Os ages are similar, suggesting that the mineralization is genetically related to the Early Cretaceous porphyry emplacement. Re contents of the molybdenites range from 21.74 to 42.45 ppm, with an average of 32.69 ppm, whereas δ³⁴S values vary between 3.7‰ and 4.2‰, which is typical of mantle sulphur. The ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/ ²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb vary in the ranges of 18.276–18.385, 15.566–15.580 and 38.321–38.382, respectively. The Taolaituo Early Cretaceous granitoids are A‐type granites. These observations indicate that the molybdenites and the porphyry granites were derived from a mixed source involving young accretionary materials and enriched subcontinental lithospheric mantle. A synthesis of geochronological and geological data reveals that porphyry emplacement and Mo mineralization in the Taolaituo deposit occurred contemporaneously with the Early Cretaceous tectonothermal events associated with lithospheric thinning, which was caused by delamination and subsequent upwelling of the asthenosphere associated with intra‐continental extension in northeast China. Copyright © 2015 John Wiley & Sons, Ltd.     

40Ar/39Ar dating,fluid inclusions and S–Pb isotope systematics of the Shabaosi gold deposit,Heilongjiang Province,China

The Shabaosi deposit is the only large lode gold deposit in the northern Great Xing'an Range. The gold ore bodies are hosted by sandstone and siltstone of the Middle Jurassic Ershi'erzhan Formation, and are controlled by three N–S‐trending altered fracture zones. The gold ore bodies are composed of auriferous quartz veinlets and altered rocks. Fluid inclusion studies indicate that the ore‐forming fluids belong to a H₂O–NaCl–CO₂–CH₄ system, with salinities between 0.83 and 8.28 wt% NaCl eq., and homogenization temperatures ranging from 180 to 320 °C. The δ³⁴S values of sulphides show a large variation from −16.9‰ to 8.5‰. The Pb isotope compositions of sulphides are characterized by a narrow range of ratios: 18.289 to 18.517 for ²⁰⁶Pb/²⁰⁴Pb, 15.548 to 15.625 for ²⁰⁷Pb/²⁰⁴Pb, and 38.149 to 38.509 for ²⁰⁸Pb/²⁰⁴Pb. The μ values range from 9.36 to 9.51. These results suggest that the ore‐forming fluids/materials were mainly of magmatic hydrothermal origin, derived from magmas produced by partial melting of the lower crust. The ⁴⁰Ar/³⁹Ar age of auriferous quartz veinlets from the Shabaosi gold deposit is about 130 Ma. The Shabaosi gold deposit has counterparts in similar orogenic gold deposits, and was formed during the post‐collisional setting of the Mongolia–Okhotsk Orogen. Copyright © 2014 John Wiley & Sons, Ltd.     

The Laqiong Sb-Au deposit: Implications for polymetallic mineral systems in the Tethys-Himalayan zone of southern Tibet,China

The Himalayan mineral field includes over 50 quartz-vein type Sb-Au deposits, and placer Au deposits. The poorly documented Laqiong deposit is a typical example of quartz-vein type Sb-Au mineralisation in Tethys Himalayan sequence. The orebody are controlled by shallow north-dipping normal faults and north–south trending faults. Magmatic zircons extracted from muscovitic leucocratic granite from the southern part of the Laqiong mine area yield a Laser Ablation-Inductively Coupled Plasma-Mass Spectrometry U-Pb age of 14 ± 1 Ma (n = 12, MSWD = 0.9) that is similar to the ⁴⁰Ar/³⁹Ar age of ca. 14 Ma from hydrothermal sericite in auriferous sulphide-quartz veins. The ε_Hf(t) values for the magmatic zircon rims range from −5.4 to −1.9, corresponding to two-stage Hf model ages of 1403–1214 Ma. Quartz from the mineralised veins has δ¹⁸O_H2O-SMOW values varying from +4.97 to +9.59‰ and δD_H2O-SMOW values ranging from −119.7 to −108.1‰. The δ¹³C_V-PDB values for calcite from the ore Stage III range from −6.9 to −5.3‰, and calcite from Stage IV are −3.5 to −1.7‰. The δ¹⁸O_V-SMOW values for calcite from Stage III are +20.3 to +20.6‰ and for Stage IV are −6.3 to −4.9‰. The stibnite and pyrite samples have ²⁰⁸Pb/²⁰⁴Pb ratios of 38.158 to 39.02, ²⁰⁷Pb/²⁰⁴Pb ratios of 15.554 to 15.698, and ²⁰⁶Pb/²⁰⁴Pb ratios of 17.819 to 18.681, and bulk and in-situ δ³⁴S_V-CDT values for stibnite, arsenopyrite and pyrite range from −1.1 to +2.3‰. The calcite from the orebodies are enriched in MREE and depleted in LREE and HREE. Fieldwork, petrological, and geochemical data collected during our study leads to the following salient findings: the mineralising fluid is a mix of magmatic and meteoric fluids; and the deposit is closely related to the emplacement of Miocene granites originating from a thickened continental crust.