Mineral Geochemistry of Apatite in the Jiama PorphyrySkarn Deposit,Tibet and its Geological Significance

The Jiama deposit,a significant porphyry-skarn-type copper polymetallic deposit located within the Gangdese metallogenic belt in Tibet,China,exemplifies a typical porphyry metallogenic system.However,the mineral chemistry of its accessory minerals remains under-examined,posing challenges for resource assessment and ore prospecting.Utilizing electron microprobe analysis and LA-ICP-MS analysis,this study investigated the geochemical characteristics of apatite in ore-bearing granite and monzogranite porphyries,as well as granodiorite,quartz diorite,and dark diorite porphyries in the deposit.It also delved into the diagenetic and metallogenic information from these geochemical signatures.Key findings include:(1)The SiO_(2) content,rare earth element(REE)contents,and REE partition coefficients of apatite indicate that the dark diorite porphyry possibly does not share a cogenetic magma source with the other four types of porphyries;(2)the volatile F and Cl contents in apatite,along with their ratio,indicate the Jiama deposit,formed in a collisional setting,demonstrates lower Cl/F ratios in apatite than the same type of deposits formed in a subduction environment;(3)compared to non-ore-bearing rock bodies in other deposits formed in a collisional setting,apatite in the Jiama deposit exhibits lower Ce and Ga contents.This might indicate that rock bodies in the Jiama deposit have higher oxygen fugacity.Nevertheless,the marginal variation in oxygen fugacity between ore-bearing and non-ore-bearing rock bodies within the deposit suggests oxygen fugacity may not serve as the decisive factor in the ore-hosting potential of rock bodies in the Jiama deposit.

Geochronology and Geochemistry of the Tinggong Porphyry Copper Ore Deposit, Tibet

We have determined the ages of the ore-bearing Tinggong porphyries and the Eocene granites using the LA-ICPMS zircon U-Pb method.Zircons from one adamellite porphyry and two diorite porphyries yield ages of 15.54±0.28 Ma,15.02±0.25 Ma and 14.74±0.22 Ma,respectively.The ages of two granites are 50.48±0.71 Ma and 50.16±0.48 Ma.Light Rare Earth Elements （LREE） are enriched in the ore-bearing adamellite porphyries,which are high-K caic-alkaline and metaluminous,while Heavy Rare Earth Elements （HREE） and Y are strongly depleted,indicating an adakitic affinity.The Large Ion Lithophile Elements （LILE） of the adamellite porphyries are highly enriched,whereas some High Field Strength Elements （HFSE） are depleted.The diorite porphyry in this study is chemically similar to the adamellite porphyries,except that the Mg# of the diorite porphyry is a little higher,demonstrating more mantle contamination.Four samples from different rocks are selected for in situ zircon Hf isotopic analyses.The samples show positive εHf（t） values and young Hf model ages,indicating their derivation from juvenile crust.However,the adamellite porphyry and diorite porphyry formed in the Miocene exhibit more heterogeneous Hf isotopic ratios,with lower （Σ）Hf （t） values than the granites formed in the Eocene,suggesting the involvement of old Indian continent crust in their petrogenesis.The geochronology and geochemistry of the adamellite porphyries and the diorite porphyries indicate that they formed from the same source region in a post-collisional environment,but contaminated by crust and mantle materials in different ratios.The metallic minerals formed mainly during the older adamellite porphyry stage,but they were recycled and reactivated by the diorite porphyry intrusion.

Geology, Geochemistry and Origin of the Hongshan Porphyry-Cryptoexplosive Breccia Type Copper Deposit in Huichang County, Jiangxi Prvince

The Hongshan porphyry-cryptoexplosive breccia type copper deposit occurs in a metamorphic rock series of the Mesoproterozoic Zhongcun Group. Orebodies are distributed inside and outside porphyry-cryptoexplosive breccia pipes. The deposit involves five ore-forming types, i.e the porphyry type, cryptoexplosive breccia type, contact-zone veinlet-disseminated type, in-pipe fracture-zone filling-replacement type and out-of-pipe fracture-zone filling-replacement type, forming an ore-forming system of “five ore-forming types within a single rock body”. Fluid inclusion and isotope geochemical studies indicate the following: S, Pb, O and Sr were derived from the lower crust, Nd was derived from the continental crust or depleted mantle and rare earth elements (REE) and trace elements have the crustal source characters; fluids consist dominantly of formation water, metamorphic water and ***meteoric water with a part of magmatic mater, heat came from porphyry while the latter originated from partial melting caused by shear heating in the lower crust and upper mantle. According to its origin the deposit is classified as the hypabyssal and near-surface, meso- and hypothermal copper deposit associated with the late Yanshanian porphyry-cryptoexplosive breccia.

Platinum-group Element Geochemistry of Magnetite from Porphyry-Cu-Mo Deposits and their Host Rocks(Siberia,Russia)

The concentrations of platinum-group elements （PGE） have been analyzed in primary magmatic magnetite samples from the Zhireken, Shakhtama and Aksug porphyry Cu-Mo deposits （Siberia, Russia） by laser ablation-inductively coupled plasma mass spectrometry to determine the range of PGE contents in magnetites and to check whether magnetite from two main rock suites （barren plutonic suite and mineralized porphyry suite） has distinct PGE composition. The results presented here indicate that magnetites are enriched in PGE relative to whole-rocks. Comparison of ore-related porphyry and barren plutonic suites shows that magnetite exhibit relatively similar PGE distribution patterns in both suites. Variations in Rh and Ru contents were controlled by the oxygen fugacity during magma crystallization.

Geochronology and Geochemistry of Metallogenetic Porphyry Bodies from the Nongping Au-Cu Deposit in the Eastern Yanbian Area, NE China: Implications for Metallogenic Environment

The metallogenetic porphyry bodies in the Nongping Au-Cu deposit, in the eastern Yanbian area, mainly include porphyritic granodiorite and biotite granodiorite porphyry. They are featured with high silicon and enrichment in sodium, and classified into sodic rocks of low-K tholeiitic basalt series. Except slightly low Sr content, the rock basically has the geochemical characteristics of the adakite： relatively high A12O3 content, relatively low MgO content, depletion in Y and Yb; relative enrichment in large ion lithophile elements （LILEs） and light rare-earth elements （LREEs）, relatively low content of high field strength elements （HFSEs）; positive Eu anomaly or weak negative Eu anomaly. In situ zircon dating technology LA-MC-ICP-MS was used to conduct single-grain zircon dating of biotite granodiorite porphyry, and the results show that the age of metallogenetic porphyry body is 100.04±0.88 Ma, indicating that the porphyry bodies were emplaced in the late Cretaceous period. According to the regional tectonic setting and the comparison with the same kind of deposits, we think that the metallogenetic porphyry bodies in the Nongping Au-Cu deposit have a close genetic connection with the subduction of the Pacific plate in the late Yanshanian period. The adakitic magma generated from partial melting of the subducting plate has high formation temperature, high oxygen fugacity, and volatile constituents＇ enrichment, so it is helpful for enrichment of metallogenetic elements and plays an important role in the formation of porphyry Au-Cu deposits in this region.

Geochronology and Geochemistry of the Mamupu Cu-Au Polymetallic Deposit,Eastern Tibet:Implications for Eocene Cu Metallogenesis in the Yulong Porphyry Copper Belt

The Mamupu skarn-type Cu-Au polymetallic deposit represents the first discovery of a medium deposit in the southern Yulong porphyry copper belt(YPCB),eastern Tibet.The Cu-Au mineralization mainly occurs as chalcopyrite in breccia,within the plate-like carbonate interlayer,being closely related to chloritization(e.g.,chlorite,magnetite and epidote)and skarnization(e.g.,diopside,tremolite and garnet).The ore-related quartz syenite porphyry(QSP)and granodiorite porphyry(GP)were emplaced at 40.1±0.2 Ma and 39.9±0.3 Ma,respectively.The QSP of Mamupu is an alkaline-rich intrusion,relatively enriched in LREE,LILE,depleted in HFSE,with no significant negative Eu and Ce anomalies,slightly high(^(87)Sr/^(86)Sr)i,lowε_(Nd)(t),uniform(^(206)Pb/^(204)Pb)i andε_(Hf)(t)values,which indicates that the porphyry magma may be caused by both the mixing of metasomatized EM II enriched mantle and thickened juvenile lower crust.The QSP in the Mamupu deposit shares a similar genesis of petrology to other ore-related porphyries within the YPCB.High oxygen fugacity and water content of the magmas are essential for the formation of porphyry and skarn Cu deposits.The QSP has similar high magmatic oxidation states and water content to the Yulong deposit,which indicates that the Mamupu has a high prospecting potential.Differences in the geological characteristics and scale of mineralization between the Mamupu and other YPCB deposits may be due to the different emplacement depths of ore-related intrusions,as well as differences in the surrounding rocks.

THE PETROCHEMISTRY AND GEOCHEMISTRY OFRICHALKALI GRANITE PORPHYRYIN WESTERN YUNNAN

The characteristics of the chemical composition of the richalkali granite porphyries are poor in SiO2, with mean content of 6919%, but rich in alkali and high in potash. The mean content of (K2O+Na2O) is 985%. K2O is much greater than Na2O, mean value of K2O/Na2O is 210. As shown by the REE analysis, REE contents is lower. Compared with the granite of south China, the richalkali granite porphyry hase higher LREE, and no anomaly of europium (δEu=087). Its genetic type belongs to A type graritoid.

U-Pb dating and geochemistry of granite porphyry dykes in the Xicha gold-(silver)deposit,southern Jilin Province,China,and their metallogenic significance

We report U-Pb dating of zircon,as well as geochemical and Hf isotope data,in order to constrain the formation time,magma source,and tectonic setting of granite porphyry dykes in the Xicha gold-(silver)district in southern Jilin Province,Northeast China.The zircon grains are euhedral-subhedral,display oscillatory growth zoning and have Th/U ratios varying between 0.11 and 0.78,which together imply a magmatic origin.The dating results indicate the porphyry formed in the Early Cretaceous(122±1 Ma)and it contains SiO2=70.64-72.31 wt%,Al2O3-=13.99-14.64 wt%,K2O+Na2O=6.96-7.81 wt%K2O/Na2O=1.24-2.10,and A/CNK=1.11-1.41.Chemically,the porphyry belongs to a high-K calc-alkaline S-type granite.Chondrite-normalized rare earth elements(REE)patterns show LREE enrichment,light rare earth elements(LREE)/heavy rare earth elements(HREE)=9.93-11.97(La/Yb)N=11.08-15.16,and d Eu=0.69-0.95.On the trace element spider diagram,large ion lithophile elements such as Rb,Ba,K,Th,and U are enriched,whereas the high field strength elements Ti and P are depleted.The e Hf(t)values of zircon from the granite porphyry vary between-17.1 and-13.2,and their Hf two-stage model ages vary from 2.01 to 2.26 Ga,implying that the magma was derived from partial melting of old lower crust.The granite porphyry dykes and many A-type granites in the region formed at the same time,suggesting an extensiona environment.The combination of the occurrence of strong magmatism,large-scale mineralization,and extensiona tectonics throughout much of Eastern China indicate that the Early Cretaceous was a period of significant lithospheric thinning.The southern Jilin Province,therefore,experienced lithospheric thinning during the Early Cretaceous.

In situ U-Pb dating and trace elements of magmatic rutile from Mujicun Cu-Mo deposit,North China Craton:Insights into porphyry mineralization

Porphyry Cu(Mo-Au)deposit is one of the most important types of copper deposit and usually formed under magmatic arc-related settings,whilst the Mujicun porphyry Cu-Mo deposit in North China Craton uncommonly generated within intra-continental settings.Although previous studies have focused on the age,origin and ore genesis of the Mujicun deposit,the ore-forming age,magma source and tectonic evolution remain controversial.Here,this study targeted rutile(TiO_(2))in the ore-hosting diorite porphyry from the Mujicun Cu-Mo deposit to conduct in situ U-Pb dating and trace element composition studies,with major views to determine the timing and magma evolution and to provide new insights into porphyry Cu-Mo metallogeny.Rutile trace element data show flat-like REE patterns characterized by relatively enrichment LREEs and depleted HREEs,which could be identified as magmatic rutile.Rutile U-Pb dating yields lower intercept ages of 139.3–138.4 Ma,interpreted as post magmatic cooling timing below about 500℃,which are consistent or slightly postdate with the published zircon U-Pb ages of diorite porphyry(144.1–141.7 Ma)and skarn(146.2 Ma;139.9 Ma)as well as the molybdenite Re-Os ages of molybdenum ores(144.8–140.0 Ma).Given that the overlap between the closure temperature of rutile U-Pb system and ore-forming temperature of the Mujicun deposit,this study suggests that the ore-forming ages of the Mujicun deposit can be constrained at 139.3–138.4 Ma,with temporal links to the late large-scale granitic magmatism at 138–126 Ma in the Taihang Orogen.Based on the Mg and Al contents in rutile,the magma of ore-hosting diorite porphyry was suggested to be derived from crust-mantle mixing components.In conjunction with previous studies in Taihang Orogen,this study proposes that the far-field effect and the rollback of the subducting Paleo-Pacific slab triggered lithospheric extension,asthenosphere upwelling,crust-mantle interaction and thermo-mechanical erosion,which jointly facilitated the formation of dioritic magmas during the Early Cretaceous.Subsequently,the dioritic magmas carrying crust-mantle mixing metallic materials were emplaced and precipitated at shallow positions along NNE-trending ore-controlling faults,eventually resulting in the formation of the Mujicun Cu-Mo deposit within an intracontinental extensional setting.

Geochemistry and Zircon U–Pb age of the Yao＇an pseudoleucite porphyry,Yunnan Province,China

The Yao'an Pb–Ag deposit, located in the Chuxiong Basin, western Yangtze Block, is an important component of the Jinshajiang–Ailaoshan alkaline porphyry–related polymetallic intrusive belt. This complex suite of rock bodies includes a vein of pseudoleucite porphyry within deposits of syenite porphyry and trachyte.The pseudoleucite is characterized by a variable greyish,greyish-white, and greyish-green porphyritic texture. Phenocrysts are mainly pseudoleucite with small amounts of alkali feldspar and biotite. In an intense event, leucite phenocrysts altered to orthoclase, kaolinite, and quartz.Both the pseudoleucite porphyry and the syenite porphyry samples were typical alkali-rich, K-rich, al-rich rocks with high LaN/YbNratios; enriched in light rare earth elements and large-ion lithophile elements, and depleted in high field strength elements; and with strongly negative Ta, Nb, and Ti(TNT) anomalies and slightly negative Eu anomalies—all characteristics of subduction-zone mantle-derived rock.We obtained a LA-ICP-MS zircon U–Pb age of 34.1 ± 0.3 Ma(MSWD = 2.4), which is younger than the established age of the Indian and Eurasian Plate collision.The magma derived from a Type-II enriched mantle formed in a post-collisional plate tectonic setting. The geochemical characteristics of the Yao'an pseudoleucite porphyry are powerful evidence that the porphyry'sdevelopment was closely linked to the Jinshajiang–Ailaoshan fault and to the Indian-Eurasian collision.

Geochemistry and zircon U-Pb chronology of quartz porphyry in Yuejinshan Fe-polymetallic deposit of Heilongjiang

Quartz porphyry in Yuejinshan Fe-polymetallic deposit is one of the rock masses, which formed the granite belt relating to the late Yanshanian skarn-type Fe-polymetallic deposits in the eastern Heilongjiang, and is also closely related to the metallogenic space of the Fe-polymetallic deposits. Quartz porphyry has the zircon U-Pb concordia age of 125.0±1.1 Ma, overall showing high Si(SiO_2=74.48%--75.00%), rich alkaline(Na_2O+K_2O=7.93%--8.17%, K_2O/Na_2O=1.39--1.46), and poor Mg(MgO=0.27%--0.31%), with the A/CNK value being 0.95--0.99, having the characteristics of obvious enrichment of LREE and medium Eu negative anomaly(0.69--0.74), indicating that the rock belongs to quasi-aluminous high potassium calc-alkaline series and has the same characteristics as those of the I-type granite. The rock is also characterized by the enrichment of LILE and active incompatible elements, and depletion of HFSE such as Nb, Ta, P and Ti, with the Mg~# value being 32--37, indicating that the rock originated from partial melting of crustal materials. It can be concluded from the above characteristics or data and from the distribution of contemporary magmatic rocks in the area, that quartz porphyry in Yuejinshan Fe-polymetallic deposit was formed in a tectonic background of the subduction of the paleo-Pacific plate in late Yanshanian.

Mineralization,Geochemistry and Zircon U-Pb Ages of the Paodaoling Porphyry Gold Deposit in the Guichi Region,Lower Yangtze Metallogenic Belt,Eastern China

The newly discovered Paodaoling porphyry Au deposit from the Guichi region, Lower Yangtze River Metallogenic Belt （LYRB）, contains 〉35 tons of Au at an average grade of -1.7 g/t. It is a porphyry ＇Au-only＇ deposit, as revealed by current exploration in the depths, mostly above -400 m, which is quite uncommon among coeval porphyry mineralization along the LYRB. Additionally, there are also Cu-Au bearing porphyries and barren alkaline granitoids in the Paodaoling district. Zircon LA-ICP-MS U-Pb dating of the Cu-Au-bearing porphyries yield an age of 141-140 Ma, falling within the main magmatic stage of the LYRB, whereas the barren granites give an age of 125-120 Ma, coeval with the regional A- type granites. The Cu-Au-bearing porphyries are LILE-, LREE-enriched and HFSE-depleted, typical of arc magmatic affinities. The barren granites are HFSE-enriched, with lower LREE/HREE ratios and pronounced negative Eu anomalies. The Cu-Au-bearing porphyries in the Paodaoling district have high oxygen fugacities and high water content. Pyrite sulfur isotopes of the Paodaoling gold deposit indicate a magmatic-sedimentary mixed source for the ore-forming fluids. Based on the alteration and poly-metal zonation of the deepest exploration drill hole from the Paodaoling Au deposit, we propose that Cu ore bodies could lie at depth beneath the current Au ore bodies. The magmatism and associated Cu-Au mineralization of the Paodaoling district are likely to have formed in a subduction setting, during slab rollback of the paleo-Pacific plate.

Geochemistry Characteristics of Granodiorite Porphyry in the Degongniuchang Copper Deposit, Muli, Sichuan Province, China

1 Introduction 1The Sanjiang region in SE Tibet Plateau and NW Yunnan is known to have formed by amalgamation of Gongwanaderived continental blocks and arc terranes as a result of oceanic subduction followed by continental

Geochronology,Geochemistry and Petrogenesis of the Bangbule Quartz Porphyry:Implications for Metallogenesis

The Bangbule skarn lead-zinc(Pb-Zn)deposit(>1 Mt Zn+Pb)is located in the western Nyainqentanglha polymetallic metallogenetic belt,central Tibet.Lenticular orebodies are all hosted in skarn and developed in the contact zone between the quartz porphyry and carbonate strata of the mid Paleozoic Middle to Upper Chaguoluoma Formation as well as in carbonate and sandstone beds of the Upper Paleozoic Laga Formation.As a newly discovered skarn deposit,the geological background and metallogenesis of this deposit remain poorly understood.Detailed petrological,geochemical and geochronological data of the ore-related quartz porphyry,helps constrain the mineralization age and contributes to discussion on the ore genesis of the Bangbule deposit.Both endoskarn and exoskarn are identified in the Bangbule deposit.From quartz porphyry to carbonate formation,the exoskarn is zoned from proximal garnet skarn to distal pyroxene skarn.Zircon U-Pb dating results show that the quartz porphyry formed at 73.9±0.8 Ma.Geochemical analysis results show that the quartz porphyry has high contents of SiO_(2)(71.40–74.94 wt%)and K_(2)O+Na_(2)O(3.76–8.46 wt%)with A/CNK values of 0.69 to 1.06.Besides,the quartz porphyry is enriched in large ion lithophile elements(LILEs)and light rare earth elements(LREEs)and have lowεNd(t)(from-8.25 to-8.19)and high initial(^(87)Sr/^(86)Sr)i values(0.713611–0.714478).Major,trace elements and whole-rock F concentration analysis results from the endoskarn samples show higher TFe_(2)O_(3),MgO,CaO,Pb+Zn,W,Sn,Mo and F etc.,and lower alkalis(K_(2)O,Na_(2)O,Sr and Ba)than those of fresh quartz porphyry,indicating that the early ore-forming fluids were an Ca-Fe-F-enriched fluid.Massive ore in the proximal skarn might be related to the high F content in the magma,which lowered the solidus temperature of the quartz porphyry magma and caused a lower temperature of the ore-forming fluids,as well as facilitating the precipitation of sphalerite and galena.Based on the geochemical characteristics presented in this study,we propose that the ore-related quartz porphyry was formed by partial melting of crust materials with some juvenile crustal component input.The partial melting of the middle-upper crust after the initial enrichment of lead and zinc elements are important for the formation of Pb-Zn deposits.The case study of the Bangbule deposit has proven that there is still a crust-derived magmatic source region in the western segment of the central Lhasa terrane.Therefore,there is still great potential for Pb-Zn mineralization and Pb-Zn exploration.

Lithogeochemistry of Intrusive Rocks in the Halo Porphyry Copper-Molybdenum Prospect, Northeast Cambodia

The Halo copper-molybdenum prospect is a porphyry system in Ratanakiri province, northeastern part of Cambodia. There is only one research was carried out on this prospect about geological mapping and short wave infrared (SWIR) spectroscopy on alteration mineral identification. The purpose of this research is to confirm the deposit type from previous Angkor Gold’s report and find the centre of porphyry deposit based on characteristic of intrusive rocks at surface and subsurface, characteristics of the intrusive rocks and alteration lithogeochemistry of intrusive and volcanic rocks by using Pearce Element Ratio (PER) analysis. PER analysis was used to examine the nature and extend of the alteration halos in the porphyry Halo copper-molybdenum prospect. The intrusive rocks and volcanic rocks in Halo, range from diorite to granite (quartz feldspar porphyry) in composition as well as dacite to trachyandesite (andesite porphyry) in composition, respectively. They were formed in a subduction-related tectonic setting, likely a volcanic arc. Trace elements spider diagrams were normalized to primitive mantle display strong enrichment in large-ion lithophile elements such as Rb, Ba and K and depletion in some high-field strength elements such as Nb and Ti, suggesting magmas generated in a subduction-related tectonic setting. PER analysis indicates a moderate to high degree of sericite alteration of dacites, quartz feldspar porphyries, andesite porphyries and granodiorite porphyries. Moreover, three alterations in the Halo prospect such as potassic (secondary K-feldspar and biotite), phyllic (sericite) and propylitic (epidote) alteration were identified, which are consistent with petrography analysis. The potassic alteration zone is vectoring center of the hydrothermal system which may represent the locus of mineralization. Therefore the geochemical signature of potassic alteration within the quartz feldspar porphyry, andesite porphyry and granodiorite porphyry with high grad of copper ranges up to 2670 ppm and molybdenum ranges up to 5297 ppm represents a character for further exploration in the Halo porphyry copper-molybdenum prospect.

Geochemistry of Rhenium and Other Trace Elements in Molybdenite,Sar Cheshmeh Porphyry Cu-Mo Deposit,Iran

LA-ICP-MS analysis of molybdenite from the Sar Cheshmeh porphyry Cu-Mo deposit(PCD),Iran,shows moderate concentration of Re(average~207 ppm)and low concentration of chalcogenides(average of Pb+Te+Bi,~31 ppm)as well as metalloids(average of As+Sb+Ge,~4.5 ppm).The early-formed quartz–molybdenites associated with potassic alteration are characterized by moderately low concentration of Re(21–215 ppm with an average of 83 ppm),whereas the transitional quartz–molybdenite veins related to the sericitic stage of mineralization contain more Re(62–465 ppm,with an average of 207 ppm).In contrast,the late-formed quartz–molybdenite veins associated with phyllic alteration show the highest concentration of Re(up to 1273 ppm with an average of 395 ppm).Gradual increase in Re content of molybdenites deposited throughout the evolution of the porphyry system is probably related to elevated fO_(2) and acidic conditions of the ore fluids governing the transitional and late stage of mineralization,when compared to the moderately low fO_(2) and basic conditions of the ore fluids precipitating the low-Re molybdenites associated with potassic alteration.The mixed mantle/crustal source of the ore-related magma and its fractionated composition in Sar Cheshmeh are consistent with magmatic conditions for the formation of Mo-rich and Re-poor PCDs in the world.

Geology,Geochemistry,and Genesis of the Tongcun Reduced Porphyry Mo(Cu) Deposit,NW Zhejiang Province,China

The Tongcun Mo（Cu） deposit in Kaihua city of Zhejiang Province,eastern China,occurs in and adjacent to the Songjiazhuang granodiorite porphyry and is a medium-sized and important porphyry type ore deposit.Two irregular Mo（Cu） orebodies consist of various types of hydrothermal veinlets.Intensive hydrothermal alteration contains skarnization,chloritization,carbonatization,silicification and sericitization.Based on mineral assemblages and crosscutting relationships,the oreforming processes are divided into five stages,i.e.,the early stage of garnet ＋ epidote ± chlorite associated with skarnization and K-feldspar ＋ quartz ± molybdenite veins associated with potassicsilicic alteration,the quartz-sulfides stage of quartz ＋ molybdenite ± chalcopyrite ± pyrite veins,the carbonatization stage of calcite veinlets or stockworks,the sericite ＋ chalcopyrite ± pyrite stage,and the late calcite ＋ quartz stage.Only the quartz-bearing samples in the early stage and in the quartzsulfides stage are suitable for fluid inclusions（FIs） study.Four types of FIs were observed,including1） CO2-CH4 single phase FIs,2） CO2-bearing two- or three-phase FIs,3） Aqueous two-phase FIs,and4） Aqueous single phase FIs.FIs of the early stages are predominantly CO2- and CH4-rich FIs of the CO2-CH4-H2O-NaCl system,whereas minerals in the quartz-sulfides stage contain CO2-rich FIs of the CO2-H2O-NaCl system and liquid-rich FIs of the H2O-NaCl system.For the CO2-CH4 single phase FIs of the early mineralization stage,the homogenization temperatures of the CO2 phase range from 15.4 ℃ to 25.3 ℃（to liquid）,and the fluid density varies from 0.7 g/cm^3 to 0.8 g/cm^3;for two- or three-phase FIs of the CO2-CH4-H2O-NaCl system,the homogenization temperatures,salinities and densities range from 312℃ to 412℃,7.7 wt%NaCl eqv.to 10.9 wt%NaCl eqv.,and 0.9 g/cm^3 to 1.0 g/cm^3,respectively.For CO2-H2O-NaCI two- or threephase FIs of the quartz-sulfides stage,the homogenization temperatures and salinities range from255℃ to 418℃,4.8 wt%NaCl eqv.to 12.4 wt%NaCl eqv.,respectively;for H2O-NaCl two-phase FIs,the homogenization temperatures range from 230 ℃ to 368 ℃,salinities from 11.7 wt%NaCl eqv.to16.9 wt%NaCl eqv.,and densities from 0.7 g/cm^3 to 1.0 g/cm^3.Microthermometric measurements and Laser Raman spectroscopy analyses indicate that CO2 and CH4 contents and reducibility（indicated by the presence of CH4） of the fluid inclusions trapped in quartz-sulfides stage minerals are lower than those in the early stage.Twelve molybdenite separates yield a Re-Os isochron age of 163 ± 2.4 Ma,which is consistent with the emplacement age of the Tongcun,Songjiazhuang,Dayutang and Huangbaikeng granodiorite porphyries.The 〈S18OSMow values of fluids calculated from quartz of the quartz-sulfides stage range from 5.6‰ to 8.6‰,and the 〈JDSMOw values of fluid inclusions in quartz of this stage range from-71.8‰ to-88.9‰,indicating a primary magmatic fluid source.〈534SV-cdt values of sulfides range from＋1.6‰ to ＋3.8‰,which indicate that the sulfur in the ores was sourced from magmatic origins.Phase separation is inferred to have occurred from the early stage to the quartz-sulfides stage and resulted in ore mineral precipitation.The characteristics of alteration and mineralization,fluid inclusion,sulfur and hydrogen-oxygen isotope data,and molybdenite Re-Os ages all suggest that the Tongcun Mo（Cu） deposit is likely to be a reduced porphyry Mo（Cu） deposit associated with the granodiorite porphyry in the Tongcun area.

Geochemistry,geochronology,and zircon Hf isotopic compositions of felsite porphyry in Xiangshan uranium orefield and its geological implication

Recently,a new kind of volcanic rock,felsite porphyry,has been revealed by drilling in Xiangshan area,Jiangxi Province,China.To better understand petrogenesis and magmatic evolution sequence of the Xiangshan volcanic-intrusive complex,we studied systematic petrology,geochemistry,LA-ICP-MS zircon U–Pb dating,and Hf isotope results of the felsite porphyry.Results show that the felsite porphyry has similar geochemical characteristics to the porphyroclastic rhyolite,which is the predominant lithology of Xiangshan uranium orefield.Felsite porphyry and porphyroclastic rhyolite have high SiO2,Al2O3,and K2O contents,low Na2O,and MgO contents,and slightly negative Eu anomalies.Moreover,these rocks are relatively depleted in large ion lithophile elements(K,Ba,and Sr)and are enriched in high field strength elements(Th,Zr,and Hf).LA-ICP-MS zircon U–Pb dating of the felsite porphyry yielded a crystallization age of 132.2±0.9 Ma,which is coeval to that of the porphyroclastic rhyolite.These ages signified that Xiangshan volcanic-intrusive complex formed in the Early Cretaceous,during which the entire South China was in the back-arc extension tectonic setting related to the subduction of the Pacific Plate under the Euroasian Plate.In-situ zircon Hf isotope data on a felsite porphyry sample show eHf(t)values from-8.82 to-5.11,while the Hf isotope two-stage model age(TDM2-Hf)ranges from 1513 to 1747 Ma.Combined with petrological,mineralogical,geochemistry,and geochronology results of the felsite porphyry,it is concluded that the felsite porphyry in Xiangshan might be originated from the partial melting of the Mesoproterozoic ancient metamorphic rocks,with possible input of small amounts of mantle materials.

Texture and Geochemistry of Multi-stage Hydrothermal Scheelite in the Mamupu Cu-Au-Mo(-W)Deposit,Eastern Tibet:Implications for Tungsten Mineralization in the Yulong Belt

Multistage tungsten mineralization was recently discovered in the Mamupu copper-polymetallic deposit in the southern Yulong porphyry copper belt(YPCB),Tibet.This study reports the results of cathodoluminescence,trace element and Sr isotope analyses of Mamupu scheelite samples,undertaken in order to better constrain the mechanism of W mineralization and the sources of the ore-forming fluids.Three different types of scheelite are identified in the Mamupu deposit:scheelite A(Sch A)mainly occurs in breccias during the prograde stage,scheelite B(Sch B)forms in the chlorite-epidote alteration zone in the retrograde stage,while scheelite C(Sch C)occurs in distal quartz sulfide veins.The extremely high Mo content and negative Eu anomaly in Sch A represent high oxygen fugacity in the prograde stage.Compared with ore-related porphyries,Sch A has a similar REE pattern,but with higher ΣREE,more depleted HREE and slightly lower(^(87)Sr/^(86)Sr)i ratios.These features suggest that Sch A is genetically related to ore-related porphyries,but extensive interaction with carbonate surrounding rocks affects the final REE and Sr isotopic composition.Sch B shows dark(Sch B-I)and light(Sch B-II)domains under CL imaging.From Sch B-I to Sch B-II,LREEs are gradually depleted,with MREEs being gradually enriched.Sch C has the highest LREE/HREE ratio,which indicates that it inherited the geochemical characteristics of fluids after the precipitation of HREE-rich minerals,such as diopside and garnet,in the early prograde stage.The Mo content in Sch B and Sch C gradually decreased,indicating that the oxygen fugacity of the fluids changed from oxidative in the early stages to reductive in the later,the turbulent Eu anomaly in Sch B and Sch C indicating that the Eu anomaly in the Mamupu scheelite is not solely controlled by oxygen fugacity.The extensive interaction of magmatic-hydrothermal fluids and carbonate provides the necessary Ca^(2+)for the precipitation of scheelite in the Mamupu deposit.

Bulk geochemistry,Rb-Sr,Sm-Nd,and stable O-H isotope systematics of the Metzimevin high-grade iron ore deposit,Mbalam iron ore district,southern Cameroon

Bulk geochemistry,Sr,Nd,and O-H isotope systematics are reported for the first time on banded iron formation(BIF)-hosted high-grade iron ore at the northwestern segment of Congo Craton(CC).Located in Mbalam iron ore district,Southern Cameroon,Metzimevin iron ore deposit is a hematite-magnetite BIF system,dominated by SiO_(2)+Fe_(2)O_(3)(97.1 to 99.84 wt%),with low concentrations of clastic elements e.g.,Al_(2)O_(3),TiO_(2),and HFSE,depicting a nearly pure chemical precipitate.The REE+Y signature of the iron deposit displays strong positive Eu anomaly,strong negative Ce anomaly,and chondritic to superchondritic Y/Ho ratios,suggestive of formation by mixed seawater-high temperature hydrothermal fluids in oxidising environment.The^(87)Sr/^(86)Sr ratios of the BIF are higher than the maximum^(87)Sr/^(86)Sr evolution curves for all Archean reservoirs(bulk silicate earth,Archean crust and Archean seawater),indicating involvement of continentally-derived components during BIF formation and alteration.TheƐ_(Nd)(t)(+2.26 to+3.77)and Nd model age indicate that chemical constituents for the BIF were derived from undifferentiated crustal source,between 3.002 and 2.88 Ga.The variable and diverse O and H isotope data(−1.9‰to 17.3‰and−57‰to 136‰respectively)indicate that the Metzimevin iron ore formed initially from magmatic plumes and later enriched by magmatic-metamorphic-modified meteoric fluids.Mass balance calculations indicate mineralisation by combined leaching and precipitation,with an average iron enrichment factor of>2.67 and SiO_(2)depletion factor of>0.99.This is associated with an overall volume reduction of 28.27%,reflecting net leaching and volume collapse of the BIF protholith.