Metallogenic Age and Ore-forming Material Sources of the Dahongshan Fe-Cu Deposit,Yunnan Province:Insights from Molybdenite Re-Os Dating and H-O-S-Pb Isotopes

The Dahongshan Fe-Cu(-Au)deposit is a superlarge deposit in the Kangdian metallogenic belt,southwestern China,comprising approximately 458 Mt of Fe ores(40%Fe)and 1.35 Mt Cu.Two main types of Fe-Cu(-Au)mineralization are present in the Dahongshan deposit:(1)early submarine volcanic exhalation and sedimentary mineralization characterized by strata-bound fine-grained magnetite and banded Fe-Cu sulfide(pyrite and chalcopyrite)hosted in the Na-rich metavolcanic rocks;(2)late hydrothermal(-vein)type mineralization characterized by Fe-Cu sulfide veins in the hosted strata or massive coarse-grained magnetite orebodies controlled by faults.While previous studies have focused primarily on the early submarine volcanic and sedimentary mineralization of the deposit,data related to late hydrothermal mineralization is lacking.In order to establish the metallogenic age and ore-forming material source of the late hydrothermal(-vein)type mineralization,this paper reports the Re-Os dating of molybdenite from the late hydrothermal vein Fe-Cu orebody and H,O,S,and Pb isotopic compositions of the hydrothermal quartz-sulfide veins.The primary aim of this study was to establish the metallogenic age and ore-forming material source of the hydrothermal type orebody.Results show that the molybdenite separated from quartz-sulfide veins has a Re-Os isochron age of 831±11 Ma,indicating that the Dahongshan Fe-Cu deposit experienced hydrothermal superimposed mineralization in Neoproterozoic.The molybdenite has a Re concentration of 99.7-382.4 ppm,indicating that the Re of the hydrothermal vein ores were primarily derived from the mantle.The δ^(34)S values of sulfides from the hydrothermal ores are 2‰-8‰ showing multi-peak tower distribution,suggesting that S in the ore-forming period was primarily derived from magma and partially from calcareous sedimentary rock.Furthermore,the abundance of radioactive Pb increased significantly from ore-bearing strata to layered and hydrothermal vein ores,which may be related to the later hydrothermal transformation.The composition of H and O isotopes within the hydrothermal quartz indicates that the ore-forming fluid is a mixture of magmatic water and a small quantity of water.These results further indicate that the late hydrothermal orebodies were formed by the Neoproterozoic magmatic hydrothermal event,which might be related to the breakup of the Rodinia supercontinent.Mantle derived magmatic hydrothermal fluid extracted ore-forming materials from the metavolcanic rocks of Dahongshan Group and formed the hydrothermal(-vein)type Fe-Cu orebodies by filling and metasomatism.

Re-Os Isotopic Dating of a W-Be Polymetallic Deposit in the Southern Qinling Region, China

Objective In recent years, a series of tungsten prospecting breakthroughs have been made in the southern Qinling Mountains. Especially, a new deposit type with a scheelite -beryl-molybdenite assemblage in the Zhen＇an area of Shaanxi Province was firstly discovered. This deposit is currently in a detailed investigation stage, and no detailed study has been yet conducted. This work selected one molybdenite sample from the Be （W） ores in this deposit for Re-Os isotope measurements to define the time limit of tungsten and beryllium mineralization, and to further reveal the ore-forming geological setting of rare metals in the southern Qinling region.

Age and metal source of orogenic gold deposits in Southeast Guizhou Province, China: Constraints from Re-Os and He-Ar isotopic evidence

The orogenic gold deposits in Southeast Guizhou are an important component of the Xuefeng polymetallic ore belt and have significant exploration potential, but geochronology research on these gold deposits is scarce. Therefore, the ore genetic models are poorly constrained and remain unclear. In the present study, two important deposits(Pingqiu and Jinjing) are investigated, including combined Re-Os dating and the He-Ar isotope study of auriferous arsenopyrites. It is found that the arsenopyrites from the Pingqiu gold deposit yielded an isochron age of 400 ± 24 Ma,with an initial ^(187)Os/^(188)Os ratio of 1.24 ± 0.57(MSWD = 0.96). An identical isochron age of 400 ± 11 Ma with an initial ^(187)Os/^(188)Os ratio of 1.55 ± 0.14(MSWD = 0.34) was obtained from the Jinjing deposit. These ages correspond to the regional Caledonian orogeny and are interpreted to represent the age of the main stage ore. Both initial ^(187)Os ratios suggest that the Os was derived from crustal rocks. Combined with previous rare earth element(REE), trace elements, Nd-Sr-S-Pb isotope studies on scheelite, inclusion fluids with other residues of gangue quartz, and sulfides from other gold deposits in the region, it is suggested that the ore metals from Pingqiu and Jinjing were sourced from the Xiajiang Group. The He and Ar isotopes of arsenopyrites are characterized by ~3 He/~4 He ratios ranging from 5.3 × 10^(-4) Ra to 2.5 × 10^(-2) Ra(Ra = 1.4 × 10^(-6), the ~3 He/~4 He ratio of air), 40 Ar=/~4 He ratios from 0.64 × 10^(-2) to 15.39×10^(-2), and ^(40)Ar/^(36)Ar ratios from 633.2 to 6582.0. Those noble gas isotopic compositions of fluid inclusions also support a crustal source origin,evidenced by the Os isotope. Meanwhile, recent noble gas studies suggest that the amount of in situ radiogenic ~4 He generated should not be ignored, even when Th and U are present at levels of only a few ppm in host minerals.

Enrichment of Platinum-group Elements(PGE) and Re-Os Isotopic Tracing for Porphyry Copper(Gold) Deposits

Platinum-group elements （PGE） in PGE-rich porphyry copper （gold） deposits are mainly Pt and Pd, whereas the concentrations of other PGE （Ru, Rh, Os, Ir） are significantly low. Moreover, Pt and Pd mainly exist in sulfides in the forms of crystal lattice or tiny platinum-group mineral （PGM） inclusions. The present data show that there is a positive relationship between Pt and Pd concentrations and Cu （Au） in porphyry copper （gold） deposits. The comparison of chondrite-normalized PGE distribution patterns between the ore-bearing porphyry intrusions and ore-barren porphyry intrusions in arc setting, 187^Os/188^Os, 87^Sr/86^Sr and S isotopes for porphyry copper （gold） deposits shows that PGEs were mainly derived from the mantle, and fluids from subduction zones devoted trivial PGE to the magma. The porphyry copper （gold） deposits associated with subducted events are most probably enriched in PGE, whereas those related to crustal thickening, lithospheric delamination or underplating rarely concentrate PGE. The osmium isotopic compositions in porphyry copper （gold） deposits reveal that （187^Os/188^Os）i values are highly variable and not lower than those of primitive upper mantle （PUM） and mantle peridotite, however, osmium concentrations are commonly lower than mantle peridotite, suggesting that parental magmas of some porphyry intrusions had experienced crustal contamination during magma evolution. Experimental investigations have proved that PGE exist in the forms of Cl^- and HS^- complexes during transportation and migration of the oreforming fluids. This paper summarizes previous studies including crucial controlling factors and mechanisms for PGE enrichment, and points out that the mantle-derived magmas parental to porphyry intrusions are the prerequisite for PGE enrichment in porphyry copper （gold） deposits. Favorable physical and chemical conditions （including salinity, temperature, pressure, pH, and oxygen fugacity） in hydrothermal fluids crucially control the PGE enrichment, and sulfur concentrations of melts play important roles in this process as well.

Re-Os Isotopic Age of Molybdenite of the Jingren Deposit and its Mineralogical Significance of Magnetite,Pyrite and Chalcopyrite

The Jingren deposit is part of the Qimantage metallogenic belt within the eastern Kunlun orogenic belt,the largest metallogenic belt in Qinghai Province,northwestern China.Exploration data show that the metal resources of the Jingren deposit are greater than 93000 t in a mining area of 76.15 km2,which indicates significant exploration potential in the near future.Three W–E-trending faults,F1-3,dominate the extension of the mineralization zone,which consists of chalcopyrite,pyrite,magnetite,galena,sphalerite,and molybdenite as well as bismuth-bearing minerals.The deposit contains a large amount of late Triassic intrusive rocks,however,previous research did not reach a consensus on the timing or the origin of the mineralization owing to a lack of geochronological data and poor exposure conditions.In the present study,Re-Os isotopic dating from six molybdenite samples collected from a borehole of the granodiorite in the Jingren deposit using negative thermal ionization mass spectrometry(NTIMS)showed 187 Re and 187 Os concentrations of 0.26–4.40 ppm and 1.03–16.46 ppb,respectively,with an initial 187 Os/188 Os value of 0.06±0.19.This proves that the Jingren deposit has a metallogenic age of(225±4)Ma and is the product of united mineralization of the Qimantage metallogenic belt and that the Jingren deposit might actually be an Indosinian metallogeny.In addition,the Re content of these samples,at 0.42 ppm to 7.00 ppm shows that the mineralization was derived mainly from a crustal source.Furthermore,electron probe microanalysis(EPMA)conducted on chalcopyrite obtained from 22 metallic mineral samples revealed(Fe+Cu)/S ratios of 1.801–1.947 with an average of 1.852,which is lower than the ideal value(1.875).Besides,the main ore body formed in a relatively higher temperature environment than the surrounding rocks in the Jingren deposit.These data indicate that the Jingren deposit formed in a metallogenic environment at lower temperature.Moreover,according to the TiO_(2)-Al_(2)O_(3)-(MgO+MnO)and TiO_(2)-Al_(2)O_(3)-MgO genetic classification diagram for magnetite,the Jingren deposit most likely belongs to the skarn family.In addition,the Co-Ni-As genetic classification diagram of the pyrite indicates sedimentary and skarn genetic characteristics.

Metallogenesis and hydrothermal evolution of the Tonggou Cu deposit in the Eastern Tianshan:Evidence from fluid inclusions,H-O-S isotopes,and Re-Os geochronology

The Tonggou Cu polymetallic deposit in the Bogda Orogenic Belt,Eastern Tianshan shows evidence for three stages of hydrothermal mineralization:early pyrite veins(Stage 1),polymetallic sulfide±epidote-quartz(Stage 2),and late-stage pyrite-calcite veins(Stage 3).Fluid inclusion petrography and microthermometry analyses indicate that the liquid-rich aqueous inclusions(L),vapour-rich aqueous inclusions(V),and NaCl daughter mineral-bearing three phase inclusions(S)formed during the main stage of mineralization,and that the ore fluids represent high-temperature and high-salinity H20-NaCl hydrothermal fluids that underwent boiling.Stable isotope(H,O)data indicate that the ore fluids of the Tonggou deposit were originally derived from magmatic water in Stage 2 and subsequently mixed with local meteoric water during Stage 3.Sulphur isotope compositions(6.7‰to 10.9‰)are consistent with theδ^34 S values of pyrite from the Qijiaojing Formation sandstone,indicating the primary source of the sulphur ore.Furthermore,chalcopyrite grains separated from the chalcopyrite-rich ore samples yield an isochron age of 303±12 Ma(MSWD=1.2).These results indicate that the Tonggou deposit is a transition between high-sulfidation and porphyry deposits which formed in the Late Carboniferous.It also suggests an increased likelihood for the occurrence of Cu(Au,Mo)in the Bogda Orogenic Belt,especially at locations where the Cu-Zn deposits are thicker;further deep drilling and exploration are encouraged in these areas.

Re-Os dating,and Pb-H-O isotope characteristics,of the Abra Cu-Ag-Pb-Au polymetallic deposit in Western Australia

The Abra deposit,a large lead-silver-copper–gold polymetallic deposit in Western Australia,is located at the eastern of the metallogenic belt of the Jillawarra basin in the Bangemall basin.The 4 th to the 6 th rock section of the Irrigully Group of Edmund Series are the principal ore-host strata,composed mainly of sandstone and fine sandstone.The orebody in Abra can be classified into two types as upper layer-like lead-silver and lower veins or netvein copper–gold.The metal minerals are mainly galena,chalcopyrite,and pyrite,while the gangue minerals are mainly quartz,dolomite,and barite.Both ReOs isotopic age of the pyrite(1329.5±98 Ma)with the initial(187Os/188Os)=5.0±3.8 and Pb isotopic compositions(206 Pb/204 Pb=15.914–15.967,207Pb/204Pb=15.425–15.454,208Pb/204Pb=35.584–35.667)suggests that the metal minerals were sourced from the wall-rocks.d DV-SMOWvalues of quartz range from-35%to-17%whereas d18 OV-SMOWvalue range from 12%to 16%which indicates that the ore-forming fluids of Abra were mediumlow temperature and medium–low salinity,and were mainly metamorphic water and secondary atmospheric precipitation.When the medium–low temperature oreforming fluids are mixed with oxidizing reducing fluids carrying a large number of metal substances,a large number of ore-forming substances will be precipitated when the physical and chemical conditions change,thus it can be considered that the Abra deposit is a medium–low temperature hydrothermal polymetallic deposit.

Re-Os and U-Pb Geochronology of the Erlihe Pb-Zn Deposit,Qinling Orogenic Belt,Central China,and Constraints on Its Deposit Genesis

The Erlihe Pb-Zn deposit is an important mine of the Pb-Zn metallogenic zone in the South Qinling Orogen.It has been considered a sedimentary exhalative deposit in previous investigations because the ore body occurs concordantly at the transitional location of an upright fold.Re and Os isotopic analyses for paragenetic pyrites with sphalerite and galena from the ore body have been used to determine the timing of mineralization and to trace the source of metallogenic materials.The Re-Os isotopic data of four pyrite samples construct an isochron,yielding a weighted average age of 226±17 Ma（mean square weighted deviation=1.7）,which is considered the main mineralization age.A dioritic porphyrite vein sample,showing weaker mineralization,was also dated using the SHRIMP zircon UPb isotopic method to constrain the youngest metallogenic age of the ore deposit,because it distributes along a group of tensional joints cutting not only the upright fold in the deposit field,but also the main ore bodies.The dioritic porphyrite sample yields a weighted mean ^（206）Pb/^（238）U age of 221±3 Ma,which is slightly younger than the Re-Os isotopic isochron age of the pyrites,considered as the upper age limit of the mineralization,namely the ending age of the mineralization.The Os isotopic compositions of sulfide minerals distribute within a range between Os isotopic compositions of the crust and the mantle, indicating that the ore deposit can be derived from magma-related fluid,and the metallogenic materials are most likely derived from the mixing source of the crust and the mantle.The Erlihe Pb-Zn deposit and associated dioritic porphyrite vein,important records of Qinling tectonic-magmatism-mineralization activities,were formed during the Triassic collisional orogeny processes.

Re-Os Dating of Molybdenite from the Yaogangxian Tungsten Deposit,South China,and Its Geological Significance

The Yaogangxian tungsten deposit is located in the central part of the Nanling polymetailic metallogenic province. The orebodies occur as veins. Wolframite and molybdenite are the dominant ore minerals. Two samples were selected for molybdenite Re-Os dating in order to elucidate the timing of mineralization. Re-Os datings of molybdenite from quartz-woiframite veins and disseminated in granite yield ages of 153±7 Ma and 163.2±4.2 Ma respectively. The results indicate that the Yaogangxian tungsten deposit is the product of large-scale metallogenesis in the middle Yanshanian period in South China, and that the evolution from late magmatic to postmagmatic hypothermal mineralization occurred at about 10 Ma. The rhenium content of molybdenite in the Yaogangxian tungsten deposit suggests that the ore materials originated from the crust.

Late Jurassic Cu-Mo Mineralization at the Zhashui-Shanyang District,South Qinling,China:Constraints from Re-Os Molybdenite and Laser Ablation-Inductively Coupled Plasma Mass Spectrometry U-Pb Zircon Dating

The Zhashui-Shanyang district is one of the most important sulfide deposits in the Qinling Orogen where the formation of porphyry-skarn Cu-Mo deposits has a close genetic link with the Yanshannian magmatism.Laser Ablation-Inductively Coupled Plasma Mass Spectrometry（LA-ICP-MS） U-Pb zircon dating of two granodiorite intrusions（Xiaohekou and Lengshuigou deposits）was investigated in the Zhashui-Shanyang district and the rock-forming ages obtained from 148.3±2.8 to 152.6±1.2 Ma,averaging 150.5 Ma,accompanied by a younger disturbance age of 144.3±1.7 Ma in the Lengshuigou intrusion,which is in excellent agreement with published sensitive high resolution ion micro-probe（SHRIMP）zircon date on the later monzodiorite porphyry phase in the Lenshuigou deposit.Two samples were selected for molybdenite ICP-MS Re-Os isotopic analyses from the Lengshuigou granodiorite porphyry,yielding Re-Os model ages from 149.2±2.7 Ma to 150.6±3.4 Ma, with a weighted mean age of 149.7±2.1 Ma.These mineralization ages overlap rock-forming ages of the host intrusions within the error range.This implies that the mineralization occurred in the Late Jurassic,which belongs to the tectonic phase B event of the Yanshan Movement,not Cretaceous as previously thought.Therefore,the Late Jurassic mineralization of the Zhashui-Shanyang district could be connected to the large-scale Yanshan molybdenum metallogenic period,the geodynamic regime of which is attributable to the far field response of convergence of surrounding plates,perhaps the approximately westward subduction of the Izanagi plate beneath the Eurasian continent.

Re-Os isotopic system and formation age of subcontinental lithosphere mantle

The determination of the formation age of subcontinental Lithosphere Mantle (SCLM) is a widely concerned issue in mantle geochemistry. it is difficult to obtain the formation age of SCLM using lithophile isotopic systems such as Rb-Sr, Sm-Nd, U-Th-Pb, ete., but as siderophile elements, the Re-Os isotopic system provides a powerful tool for that work. Here a comprehensive review on the recent development in Re-Os dating for SCLM has been given.

Genesis of the Huoshenmiao Mo deposit in the Luanchuan ore district, China: Constraints from geochronology, ?uid inclusion, and H-O-Sisotopes

The Huoshenmiao δeposit is Mo skarn δeposit, located in the western part of the Luanchuan ore δistrict.Mineralization process can be δivided into a skarn and a quartz-sulfide episodes with six stages: prograde(I), retrograde(II), quartz-K-feldspar(III), quartz-molybdenite(IV), quartz-pyrite(V), and quartzcalcite(VI). A combined study of geochronology, fluid inclusion(FI), and stable isotopes was conducted to constrain the mineralization age, source of ore materials, as well as the origin and evolution of the ore-forming fluids. Molybdenite Ree Os δating indicates that the δeposit was formed in the Late Jurassic(~145 Ma). The δ^(34)S values of sulfides range from 3.0‰ to 7.1‰, implying that the ore materials in the δeposit are magmatic in origin. Three types and six subtypes of FIs are δistinguished, namely, aqueous two-phase(W_1-and W_2-type), δaughter mineral-bearing multiphase(S_1-and S_2-type), and CO_2-bearing three-phase(C_1-and C_2-type). In stages I and II, the W_1-type FIs δisplay homogenization temperatures(Th) from 496°C to >600°C, with salinities of 14.9-18.3 wt.% NaCl eqv. The FIs in stages III, IV and early stage V composed of coeval S-, C-and W-types, respectively homogenize at similar Th, suggesting the occurrence of boiling. The W1-type FIs in late stage V and stage VI, yield Th of 102-406°C and salinities of 0-4.7 wt.% NaCl eqv. The δD_(H_2O)and δ^(18) O(H_2O)values of the ore-forming fluids in quartz-sulfide episode vary from-112‰ to-76‰, and 11.0‰ to 1.0‰, respectively. All these above observations reveal that the early ore-forming fluids are magmatic in origin, and characterized by high temperature and moderate to high salinity, and gradually evolve to low temperature, low salinity meteoric water. The Huoshenmiao Mo δeposit is associated with the magmatism event induced by the protracted subduction of the Izanagi plate beneath the eastern China continent. The δecrease in temperature, salinity and f(O_2), as well as change of p H δue to boiling and fluid-rock interaction, are the main factors controlling Mo δeposition.

Re-Os isotopic composition of the Dongling ⅢCD iron meteorite

Re, Os concentrations and Os isotopic compositions of the Dongling ⅢCD iron meteorite were determined by N-TIMS technique. The result was compared with that of the other irons and chondrites. The Re and Os concentrations of the Dongling iron meteorite were plotted on the trends of the group ⅢA and ⅣA irons. The Pt-Os relation of the Dongling iron meteorite is similar to that of the group ⅡA irons. That suggests a higher fractionation for the Dongling iron meteorite.

Timing and Source of the Hermyingyi W-Sn Deposit in Southern Myanmar, SE Asia: Evidence from Molybdenite Re-Os Age and Sulfur Isotopic Composition

The Hermyingyi W-Sn deposit, situated in southern Myanmar, SE Asia, is a typical quartz-vein type W-Sn deposit. The ore-bearing quartz veins are mainly hosted by the Hermyingyi monzogranite which intruded into the Carboniferous metasedimentary rocks of Mergui Series. According to mineral assemblages and crosscutting relationships, four ore-forming stages are recognized:(1) silicate-oxide stage;(2) quartz-sulfide stage;(3) barren quartz vein stage;(4) supergene stage. Five molybdenite samples from the deposit yield Re-Os model ages ranging from 67.8±1.6 to 69.2±1.6 Ma(weighted mean age of 68.7±1.2 Ma), and a well-defined isochron age of 68.4±2.5 Ma(MSWD=0.18, 2σ). This Re-Os age is consistent with the previously published zircon U-Pb age of the Hermyingyi monzogranite(70.0±0.4 Ma)(MSWD=0.9, 2σ) within errors, which indicates a genetic link between the monzogranitic magmatism and W-Sn mineralization. The new high-precision geochronological data reveal that the granitic magmatism and associated W-Sn mineralization in southern Myanmar took place during the Late Cretaceous(70–68 Ma). The extremely low Re contents(22.9 ppb to 299 ppb) in molybdenite, coupled with sulfide δ^(34)S values in the range of +1.9‰ to +5.6‰ suggest that ore-forming metals were predominately sourced from the crustal-derived granitic magma.

Sulfide Aggregation in Ophiolitic Dunite Channels Explains Os-Isotope Mismatch between Oceanic Crust and Mantle

The osmium-isotope mismatch commonly reported between mid-ocean-ridge basalts(MORBs) and residual mantle might reflect evolution of the MORB Re-Os system after extraction from the asthenosphere, or preferential contribution of radiogenic Os components from mantle. However, in a MOR system, the role of dunite melt channels from the upper mantle and Moho transition zone in regulating isotopic systems between mantle and crust has rarely been evaluated. We report new Re-Os isotopic compositions of base-metal sulfides(BMS), chromites and dunites from dunite lenses with low spinel Cr# [Cr3+/(Cr3++Al3+) ≤ 0.66](products of interaction between MORB-like melts and upper-mantle harzburgites) from the Zedang ophiolite(South Tibet). Re-Os isotopic compositions of low-Cr# dunites from the Oman ophiolite are also shown for comparison. Mineralogical evidence suggests that the Zedang sulfides were originally precipitated as monosulfide solid solutions. The highly variable 187Os/188Os initial ratios(0.1191-0.1702) and low 187Re/188Os(<0.22) of the sulfides suggest that the chromite acted as a sink for Os-bearing sulfides, aggregating discrete Os components with heterogeneous isotopic signatures from asthenospheric or lithospheric mantle into dunite channels. The Zedang chromites and dunites show 187Os/188Os ratios similar to the primitive upper mantle(PUM), except for two dunites with sub-PUM ratios, reflecting the contribution of Os balanced by smaller volumes of Os-rich, unradiogenic sulfides(likely nucleating on Os nanoparticles) and larger volumes of Os-poor radiogenic BMS. Such isotopic heterogeneity, despite with less variation, has been observed in dunite channels from the Oman ophiolite and present-day mid-ocean ridges. Formation of dunite channels in the upper mantle thus can aggregate Os-bearing sulfides with chromite, leaving high Re/Os components into the residual melts. Once such channel systems were built up at the crust-mantle transition zone, the newly incoming MOR magmas would preferentially melt and dissolve the volumetrically abundant radiogenic BMS and retain Os-rich nanoparticles in the channels, further amplifying the Os-isotope mismatch between oceanic crust and mantle. This study sheds new light on the multistage evolution and small-scale behaviors of chalcophile and siderophile elements(e.g., Re-Os) and their isotopes(e.g., 187Re-187Os) with sulfides and chromites in a silicate-dominated melt plumbing system beneath mid-ocean ridges.

Re-Os isotope dating of molybdenites in the Huang-shaping Pb-Zn-W-Mo polymetallic deposit, Hunan Province, South China and its geological significance

The large-scale Huangshaping Pb-Zn-W-Mo polymetallic deposit is located in the central Nanling min- eralization zone, South China. Six molybdenite samples from the Huangshaping deposit were selected for Re-Os isotope measurement in order to define the mineralization age of the deposit. It yields a Re-Os isochron age of 154.8±1.9 Ma (2σ ), which is in accordance with the Re-Os model ages of 150.9― 156.9 Ma. This age is about 7 Ma younger than their host granite porphyry, which was dated as 161.6±1.1 Ma by zircon U-Pb method using LA-ICPMS. All these ages demonstrate that the Huang- shaping granite and related Pb-Zn-W-Mo deposit occurred in the middle Yanshanian period, when many other granitoid and related ore deposits emplaced and formed, e.g. the Qitianling granite and Furong tin deposit, the Qianlishan granite and giant Shizhuyuan W-Sn-Mo-Bi deposit and Jinchuantang Sn-Bi deposit in the nearby area. They constitute the main part of the magmatic-metallogenic belt of southern Hunan, and represent the large-scale metallogeny in middle Yanshanian in the area. The lower rhenium content in molybdenite of Huangshaping deposit suggests that the ore-forming material was mainly of crust origin.

Re-Os and Nd isotopes of black shales at the bottom of the Lower Cambrian from the northern Tarim Platform and their comparison with those from the Yangtze Platform

This paper reports Re-Os and Nd isotopes of black shales at the bottom of Lower Cambrian from the northern Tarim Basin and traces source materials of the black shales through isotopes. The average Re/Os, 187Re/188Os, and 187Os/188Os ratios of the black shales at the bot-tom of Lower Cambrian from the Tarim Basin are 7.18, 5.6438, and 1.9616, respectively. These isotopic ratios suggest the crustal sources of the black shales. The e Nd(0) value is 13.17, the e Nd(540 Ma) value is 7.32 and the Nd model ages are 1.535 Ga. These parameters in the black shales are quite consistent with those from the basement rocks. Based on the Re-Os and Nd isotopic characteristics of the black shales, we conclude that the continental crust mainly composed of basement rocks is the source material of the black shales. Through comparison of these isotopic parameters with those from the Yangtze Platform, it is clear that the Re-Os isotopic characteristics in the black shales from the Tarim and Yangtze platforms are quite different, which maybe indicates the differences in depositional settings between two platforms. These Re-Os isotopic data provide us with constraints to analyze the genetic relation between the two plat-forms.

Cretaceous Meteorite Impact-Induced Initial Subduction:Records of highly Siderophile Element Abundances and Re-Os Isotopes in Ophiolites

Compiled global ophiolite data reveal that Cretaceous ophiolites exhibit broaden variations in 187Re/188Os and ^(187)Os/^(188)Os values,increases in Re concentrations and thus Re/Os ratios in all peridotites and chromitites,and additional increased PPGE/IPGE(Pd-subgroup platinum-group element(PGE)/Ir-subgroup PGE)ratios in chromitites and dunites relative to pre-Cretaceous ophiolites.These compositional changes in Cretaceous ophiolites,which mostly formed in subduction initiation settings,cannot be attributed solely to involvement of subducting or previously subducted crustal materials.Here,the author proposes a Cretaceous meteorite impact model that led to impact-induced disruption of oceanic lithosphere,asthenosphere upwelling,subduction initiation at edges of laterally spreading anomalies.High-pressure and high-temperature conditions during the impacts caused melting of the meteorites and the ambient crustal and mantle rocks,producing hybrid melts containing partially un-melted fragments.Crustal materials contributed to the elevated ^(187)Os/^(188)Os values,Re and Re/Os ratios,whereas the undifferentiated meteorite accounted for the increases in the PPGE/IPGE and decreased ^(187)Os/^(188)Os ratios.Shock pressure and super-reduced phases were likely generated by this process and were subsequently transported into the newly formed mantle peridotites and chromitites of future ophiolites.The remaining meteoritic and lithospheric fragments most likely sank deeper and were distributed widely in the convecting mantle to produce the observed global compositional heterogeneities.

Mineralization episode of porphyry copper deposits in the Jinshajiang-Red River mineralization belt: Re-Os dating

Re-Os isotopic dating for the molybdenites from the porphyry copper deposits of the Jinshajiang-Red River mineralization belt in Yunnan Province yields isochron ages of 33.9±1.1 Ma for the Machangqing deposit and 34.4±0.5 Ma for the Tongchang deposit. This result shows that both the Machangqing and the Tongchang porphyry Cu-Mo deposits from two different ore-fields formed simultaneously. This new data and the published Re-Os model ages of molybdenite (35.4 Ma, 35.9 Ma, 36.2 Ma) of the Yulong porphyry copper deposit in Tibet, which is located in the same Jinshajiang-Red River mineralization belt as the Machangqing deposit and the Tongchang deposit, suggest that these three Cenozoic porphyry copper deposits in the Jinshajiang-Red River mineralization belt were contemporary for their mineralization episode. That is to say, even their present locality is far away and nearly iso-distantly distributed, these three porphyry Cu(Mo) deposits belong to the same mineralization episode at the end of Eocene.

Re-Os Dating of Galena and Sphalerite from Lead-Zinc Sulfide Deposits in Yunnan Province, SW China

Dating of lead-zinc deposits is of critical importance for better understanding of ore genesis, but has long been a big challenge due to the lack of suitable minerals that can be unequivocally linked to the ore genesis and that can be used for tradition radiometric methods. This kind of deposits have simple mineralogy dominated by galena and sphalerite commonly associated with calcite and other gangue minerals. Both galena and sphalerite have low and high variable Re concentrations and thus Re-Os dating of these minerals have been less promising. In addition, the recovery of Re is extremely low for galena when conventional method was applied, lending additional difficulty in precisely dating galena. In this study, we investigate the recovery of Re using different media for anion exchange separation and reporte a revised preparation method for Re-Os dating of galena and sphalerite. By using the new protocol, two reliable Re-Os isochron ages of galena and sphalerite from the Fule（20.4±3.2 Ma） and Laochang（308±25 Ma） Pb-Zn deposits in Yunnan Province, SW China, are achieved.