Geochemical and mineralogical characteristics of weathered ore in the Dalucao REE deposit,Mianning–Dechang REE Belt,western Sichuan Province,southwestern China

The Dalucao deposit in western Sichuan Province, southwest China, is one of the largest and most extensive rare earth element (REE) deposits in the Himalayan Mianning–Dechang REE Belt. Moreover, this is the only deposit identified in the southern part of the belt. The deposit contains the No. 1, 2, and 3 orebodies. The No. 1 and 3 orebodies are hosted in two breccia pipes within syenite–carbonatite rocks that intrude a Proterozoic quartz–diorite pluton. Both breccia pipes have elliptical horizontal cross-sections at the surface, being 200–400 m long, 180–200 m wide, and extending to > 450 m depth. The No. 1 and No. 3 orebodies have total thicknesses of 55–175 m and 14–58 m, respectively. REE mineralization is associated with four brecciation events that are recorded in both pipes. The ore grades in the No. 1 and 3 orebodies are similar, with the rocks containing 1.0–4.5% rare earth oxides (REOs). The No. 1 orebody is characterized by a mineral assemblage comprising fluorite + barite + celestite + bastnäsite (i.e., Type I), whereas the No. 3 orebody is characterized by an assemblage comprising fluorite + celestite + pyrite + muscovite + bastnäsite + strontianite (i.e., Type II). Significant amounts of weathered high-grade REE ore (up to 60 wt.% of the rock mass) is mainly present in the No. 1 orebody. This is the main ore-type targeted for exploration within the Dalucao deposit, but is rarely present in other deposits in the Mianning–Dechang REE Belt.Faulting and cryptoexplosive breccia events, possibly linked to movement on the Panxi Fault, were more common in the No. 1 orebody than in the No. 3 orebody. This facilitated the introduction of ore-forming hydrothermal fluids and provided space for the precipitation of REE minerals. Based on the present results, we infer that the Dalucao deposit was the product of multiple stages of ore formation. REE minerals formed in envelopes around, or fractures within, quartz, fluorite, calcite, barite, and celestite in the brecciated ores. The main REE minerals were deposited from hydrothermal fluids within cryptoexplosive breccia, followed by weathering that increased the ore grade. Petrographic studies and X-ray powder diffraction (XRD) analyses indicate that the weathered ore contains 5–60% REE minerals (including bastnäsite, parisite, and monazite), together with gangue (quartz, barite, celestite, and fluorite), large amount of clay minerals (smectite, illite, kaolinite, and sepiolite), and relict igneous minerals (quartz, albite, and K-feldspar). The weathered samples are strongly enriched in La (up to 92,390 ppm), Ce (up to 103,500 ppm), Pr (up to 8006 ppm), and Nd (up to 16,690 ppm) compared with the unweathered brecciated ores. Conversely, Sr concentrations are significantly more enriched in the brecciated ores (up to 256,500 ppm) than in the weathered ores (generally less than 2671 ppm with one exception of 37,850 ppm) due to less celestite. Calcite is largely absent from the weathered ores (except one sample with up to 30% mode), which contrasts with the brecciated ores that contain up to 75% calcite. The effects of weathering, oxidation, loss of ions, and hydration on the brecciated ores led to the refertilization of the REEs and an increase in the grade of the ore deposit.     

Cadmium and sulfur isotopic compositions of the Tianbaoshan Zn–Pb–Cd deposit,Sichuan Province,China

Although Zn–Pb deposits are one of the most important Cd reservoirs in the earth, few studies have focused on the Cd isotopic fractionation in Zn–Pb hydrothermal systems. This study investigates the causes and consequences of cadmium and sulfur isotope fractionation in a large hydrothermal system at the Tianbaoshan Zn–Pb–Cd deposit from the Sichuan–Yunnan–Guizhou (SYG) metallogenic province, SW China. Moderate variations in Cd and S isotope compositions have been measured in sphalerite cover a distance of about 78 m. Sphalerite has δ^114/110Cd values ranging from 0.01 to 0.57‰, and sulfides (sphalerite, galena and chalcopyrite) have δ³⁴S_CDT values ranging from 0.2 to 5.0‰. Although δ³⁴S_CDT and δ^114/110Cd values in sphalerites have no regular spatial variations, the δ³⁴S_CDT values in galena and calculated ore-forming fluid temperatures decreased from 2.1 to 0.2‰ and from about 290 to 130 °C, respectively, from the bottom to the top of the deposit. Heavy Cd isotopes are enriched in early precipitated sphalerite in contrast to previous studies. We suggest that Cd isotopic compositions in ore-forming fluids are heterogeneous, which result in heavy Cd isotope enrichment in early precipitated sphalerite. In comparison with other Zn–Pb deposits in the SYG area, the Tianbaoshan deposit has moderate Cd contents and small isotope fractionation, suggesting differences in origin to other Zn–Pb deposits in the SYG province.In the Tianbaoshan deposit, the calculated δ³⁴S∑_S-fluids value is 4.2‰, which is not only higher than the mantle-derived magmatic sulfur (0 ± 3‰), but also quite lower than those of Ediacaran marine sulfates (about 30 to 35‰). Thus, we suggest that reduced sulfur of ore-forming fluids in the deposit was mainly derived from the leaching of the basement, which contains large amount of volcanic or intrusive rocks. Based upon a combination of Cd and S isotopic systems, the Tianbaoshan deposit has different geochemical characteristics from typical Zn–Pb deposits (e.g., the Huize deposit) in SYG area, indicating the unique origin of this deposit.     

K–Ar ages of plutonism and mineralization at the Shizhuyuan W–Sn–Bi–Mo deposit,Hunan Province,China

The Qianlishan granite complex, situated 16 km southeast of Chenzhou City, Hunan Province, China, hosts the Shizhuyuan W–Sn–Bi–Mo deposit. This complex, which intruded the Protozoic metasedimentary rocks and the Devonian clastic sedimentary and carbonate rocks, consists of mainly medium- to coarse-grained biotite granites and minor amounts of fine-grained biotite granite in addition to granite and quartz porphyry. K–Ar ages suggest three episodes of plutonism: the medium- to coarse-grained biotite granite (before 152 Ma), the fine-grained biotite granite (137 Ma), and the granite porphyry (129–131 Ma). Muscovite ages of the greisen are 145–148 Ma, suggesting that the W–Sn–Bi–Mo mineralization was related to the main, medium- to coarse-grained biotite granites. The K–Ar age of the hydrothermal vein mineralization is 92 Ma and is probably related to the porphyries.     

Geochemical characteristics of acid mine drainage and sediments from coal mines, Shanxi Province, China

In this study, geochemical characteristics of acid mine drainage （AMD） and its sediments from the Malan and Sitai coalmines, Shanxi Province, China, were investigated. Many analytical approaches such as IC, ICP-MS, XRD, XRF, and modeling calculation of hydrogeochemistry using PHREEQCI software were employed. The AMD is characterized by higher concentrations of iron and sulfate, a low pH, and elevated concentrations of a wide variety of heavy metals. The results of modeling calculation by PHREEQCI software demonstrate the metals in AMD are present mainly as Me^n＋ and MeSO4^n-2 species. The sediments of AMD are composed mainly of iron-beating minerals such as goethite and schwertmannite, which are controlled by pH, Fe and SO4^2- concentrations. The schwertmannite mineral has been found for the first time in China.     

REE characteristics of the Fanshan alunite deposit in Zhejiang Province, China

1 Introduction Alunite [KAl3(SO4)2(OH)6] is a very important non-ferrous metal resource, so many countries throughout the world have made great investments in research on the mechanism of its formation, its geological characteristics and applications. O…     

Geochemical Characteristics and Genesis of Pyrite from the Dongguashan Cu-Au Deposit, Anhui Province, China

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The mixing of multi-source fluids in the Wusihe Zn–Pb ore deposit in Sichuan Province,Southwestern China

The Sichuan–Yunnan–Guizhou (SYG) metallogenic province of southwest China is one of the most important Zn–Pb ore zones in China, with ~ 200 Mt Zn–Pb ores at mean grades of 10 wt.% Zn and 5 wt.% Pb. The source and mechanism of the regional Zn–Pb mineralization remain controversial despite many investigations that have been conducted. The Wusihe Zn–Pb deposit is a representative large-scale Zn–Pb deposit in the northern SYG, which mainly occurs in the Dengying Formation and yields Zn–Pb resources of ~ 3.7 Mt. In this paper, Zn and S isotopes, and Fe and Cd contents of sphalerite from the Wusihe deposit were investigated in an attempt to constrain the controls on Zn and S isotopic variations, the potential sources of ore-forming components, and the possible mineralization mechanisms. Both the δ⁶⁶Zn and δ³⁴S values in sphalerite from the Wusihe deposit increase systematically from the bottom to the top of the strata-bound orebodies. Such spatial evolution in δ⁶⁶Zn and δ³⁴S values of sphalerite can be attributed to isotopic Rayleigh fractionation during sphalerite precipitation with temperature variations. The strong correlations between the Zn–S isotopic compositions and Fe–Cd concentrations in sphalerite suggest that their variations were dominated by a similar mechanism. However, the Rayleigh fractionation mechanism cannot explain the spatial variations of Fe and Cd concentrations of sphalerite in this deposit. It is noted that the bottom and top sphalerites from the strata-bound orebodies document contrasting Zn and S isotopic compositions which correspond to the Zn and S isotopic characteristics of basement rocks and host rocks, respectively. Therefore, the mixing of two-source fluids with distinct Zn–S isotopic signatures was responsible for the spatial variations of Zn–S isotopic compositions of sphalerite from the Wusihe deposit. The fluids from basement rocks are characterized by relatively lighter Zn (~ 0.2 ‰) and S (~ 5 ‰) isotopic compositions while the fluids from host rocks are marked by relatively heavier Zn (~ 0.6 ‰) and S (~ 15 ‰) isotopic compositions.

     

Metallogenic efficiency from deposit to region–A case study in western Zhejiang Province,southeastern China

Metallogenic (ore) efficiency can be defined as the ratio of metal reserves to its total supply, and we expanded a typical efficiency-calculation model available at the single mineral scale to the regional scale. A new cell-based model was developed by analogy and by taking some other influences into account: i) a thicker sedimentary cover; ii) regional ore- and rock-controlling structures and their intersections; iii) the crustal heterogeneity unrelated and related to ores; and iv) metallic geochemical anomalies. Finally, a regional contour map of weighted efficiency, which is essential to metallogenic prediction, was obtained. It shows that the efficiency anomalies can provide a much better target area for ore-positioning than do metallic content anomalies, and greater ore efficiency may indicate the likelihood of occurrence of mineral deposits that are larger in size (reserves). Taking northwestern Zhejiang province as a case study, in which the geochemistry of Mesozoic porphyries plausibly show considerable mineralized potential, we found that due to the lower magmatic temperature, delayed exsolution of the hydrothermal solution, and very thick sedimentary cover, the Cu-polymetal ore efficiency associated with granitic plutons in this area is generally low; the relatively higher ore-productivity (efficiency) appears mainly in and around small rock bodies, rock margins, and the contacting zone between different lithologies. Most ore spots, no matter their size, fall into areas with nonzero efficiency values. There seems to be no interdependence between most ore spots of smaller size and ore efficiency, whereas efficiency is essential to regional small- and medium-scaled metallogensis.     

Geological,geochemical, and geochronological characteristics of Caledonian W–Sn mineralization in the Baiganhu orefield,southeastern Xinjiang,China

The newly discovered large-scale Baiganhu W–Sn orefield, consisting of the Kekekaerde, Baiganhu, Bashierxi, and Awaer deposits, is located in Ruoqiang County, southeastern Xinjiang, China. These deposits comprise mainly three types of W–Sn mineralization: early-stage skarn-type, middle-stage greisen-type, and late-stage quartz-vein-type. In this study, we classified seven major vertical zones on the basis of petrographic characteristics, roughly from the bottom of the parental granitic intrusions upward, as (A) fresh syenogranite, (B) argillic alteration, (C) muscovite-dominated greisenization, (D) tourmaline-dominated greisenization, (E) marginal facies (including K-feldspar pegmatite and fine-grained granite), (F) aplitic apophysis, and (G1) skarn or (G2) infilled silification zones. According to the alteration–mineralization assemblages and cross-cutting relationships, five stages of mineralization are recognized in the orefield (I, skarn stage; II, greisen stage; III, quartz vein stage; IV, argillic alteration stage; and V, supergene stage), and reverse alteration zonation in the altered intrusion is also observed.The W–Sn deposits are spatially associated with syenogranite, which is part of the Caledonian Bashierxi magmatic series. Laser ablation–inductively coupled plasma–mass spectrometry (LA-ICP-MS) zircon U–Pb dating of the syenogranite yields a weighted mean ²⁰⁶Pb/²³⁸U age of 413.6 ± 2.4 Ma (MSWD = 0.36, n = 30). Hydrothermal muscovite from three samples associated with W–Sn mineralization yields plateau ⁴⁰Ar/³⁹Ar ages of 411.7 ± 2.6 Ma (MSWD = 0.21), 412.8 ± 2.4 Ma (MSWD = 0.22), and 413.8 ± 2.6 Ma (MSWD = 0.22), which is consistent with the zircon U–Pb age, thus indicating a temporal link between the emplacement of the syenogranite and the W–Sn mineralization. Our age data and previously published ages, along with geochemical data, for the granitoids in the Bashierxi magmatic series show a nearly contemporaneous evolution of A- and S-type granites, which were emplaced in a post-orogenic setting at ca. 432–413 Ma. As compared with the A-type granites, the syenogranites with S-type affinities probably resulted from a lower degree of partial melting of metagreywackes, which was more likely to be enriched in the ore-forming elements W and Sn, as well as volatiles such as B and H₂O. In addition, the syenogranites exhibit low oxidation states and underwent high degrees of factional crystallization, both of which favor post-magmatic W–Sn mineralization. We suggest that more attention should be given to buried syenogranites of S-type affinities during mineral exploration in this area, and that the proposed model of a vertical alteration zoning can act as a guide to the targeting of similar ore systems.     

Zircon U–Pb,molybdenite Re–Os and muscovite Ar–Ar isotopic dating of the Xitian W–Sn polymetallic deposit,eastern Hunan Province,South China and its geological significance

The Xitian tungsten–tin (W–Sn) polymetallic deposit, located in eastern Hunan Province, South China, is a recently explored region containing one of the largest W–Sn deposits in the Nanling W–Sn metallogenic province. The mineral zones in this deposit comprise skarn, greisen, structurally altered rock and quartz-vein types. The deposit is mainly hosted by Devonian dolomitic limestone at the contact with the Xitian granite complex. The Xitian granite complex consists of Indosinian (Late Triassic, 230–215 Ma) and Yanshanian (Late Jurassic–Early Cretaceous, 165–141 Ma) granites. Zircons from two samples of the Xitian granite dated using laser ablation-inductively coupled mass spectrometer (LA-ICPMS) U–Pb analysis yielded two ages of 225.6 ± 1.3 Ma and 151.8 ± 1.4 Ma, representing the emplacement ages of two episodic intrusions of the Xitian granite complex. Molybdenites separated from ore-bearing quartz-veins yielded a Re–Os isochron age of 149.7 ± 0.9 Ma, in excellent agreement with a weighted mean age of 150.3 ± 0.5 Ma. Two samples of muscovites from ore-bearing greisens yielded ⁴⁰Ar/³⁹Ar plateau ages of 149.5 ± 1.5 Ma and 149.4 ± 1.5 Ma, respectively. These isotopic ages obtained from hydrothermal minerals are slightly younger than the zircon U–Pb age of 151.8 ± 1.4 Ma of the Yanshanian granite in the Xitian area, indicating that the W–Sn mineralization is genetically related to the Late Jurassic magmatism. The Xitian deposit is a good example of the Early Yanshanian regional W–Sn ore-forming event (160–150 Ma) in the Nanling region. The relatively high Re contents (8.7 to 44.0 ppm, average of 30.5 ppm) in molybdenites suggest a mixture of mantle and crustal sources in the genesis of the ore-forming fluids and melts. Based upon previous geochemical studies of Early Yanshanian granite and regional geology, we argue that the Xitian W–Sn polymetallic deposit can be attributed to back-arc lithosphere extension in the region, which was probably triggered by the break-off of the flat-slab of the Palae-Pacific plate beneath the lithosphere.     

Geochemical Characteristics of Trace Elements of Zoige 510-1 Uranium Deposit, Sichuan Province, China

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Genesis of the Huangshaping W–Mo–Cu–Pb–Zn polymetallic deposit in Southeastern Hunan Province,China: Constraints from fluid inclusions,trace elements,and isotopes

The Huangshaping polymetallic deposit is located in southeastern Hunan Province, China. It is a world-class W–Mo–Pb–Zn–Cu skarn deposit in the Nanling Range Metallogenic Belt, with estimated reserves of 74.31 Mt of W–Mo ore at 0.28% WO₃ and 0.07% Mo, 22.43 Mt of Pb–Zn ore at 3.6% Pb and 8.00% Zn, and 20.35 Mt of Cu ore at 1.12% Cu. The ore district is predominantly underlained by carbonate formations of the Lower Carboniferous period, with stocks of quartz porphyry, granite porphyry, and granophyre. Skarns occurred in contact zones between stocks and their carbonate wall rocks, which are spatially associated with the above-mentioned three types of ores (i.e., W–Mo, Pb–Zn, and Cu ores).Three types of fluid inclusions have been identified in the ores of the Huangshaping deposit: aqueous liquid–vapor inclusions (Type I), daughter-mineral-bearing aqueous inclusions (Type II), and H₂O–CO₂ inclusions (Type III). Systematic microthermometrical, laser Raman spectroscopic, and salinity analyses indicate that high-temperature and high-salinity immiscible magmatic fluid is responsible for the W–Mo mineralization, whereas low-temperature and low-salinity magmatic-meteoric mixed fluid is responsible for the subsequent Pb–Zn mineralization. Another magmatic fluid derived from deep-rooted magma is responsible for Cu mineralization.Chondrite-normalized rare earth element patterns and trace element features of calcites from W–Mo, Pb–Zn, and Cu ores are different from one another. Calcite from Cu ores is rich in heavy rare earth elements (187.4–190.5 ppm), Na (0.17%–0.19%), Bi (1.96–64.60 ppm), Y (113–135 ppm), and As (9.1–29.7 ppm), whereas calcite from W–Mo and Pb–Zn ores is rich in Mn (> 10.000 ppm) and Sr (178–248 ppm) with higher Sr/Y ratios (53.94–72.94). δ¹⁸O values also differ between W–Mo/Pb–Zn ores (δ¹⁸O = 8.10‰–8.41‰) and Cu ores (δ¹⁸O = 4.34‰–4.96‰), indicating that two sources of fluids were, respectively, involved in the W–Mo, Pb–Zn, and Cu mineralization.Sulfur isotopes from sulfides also reveal that the large variation (4‰–19‰) within the Huangshaping deposit is likely due to a magmatic sulfur source with a contribution of reduced sulfate sulfur host in the Carboniferous limestone/dolomite and more magmatic sulfur involved in the Cu mineralization than that in W–Mo and Pb–Zn mineralization. The lead isotopic data for sulfide (galena: ²⁰⁶Pb/²⁰⁴Pb = 18.48–19.19, ²⁰⁷/²⁰⁴Pb = 15.45–15.91, ²⁰⁸/²⁰⁴Pb = 38.95–39.78; sphalerite: ²⁰⁶Pb/²⁰⁴Pb = 18.54–19.03, ²⁰⁷/²⁰⁴Pb = 15.60–16.28, ²⁰⁸/²⁰⁴Pb = 38.62–40.27; molybdenite: ²⁰⁶Pb/²⁰⁴Pb = 18.45–19.21, ²⁰⁷/²⁰⁴Pb = 15.53–15.95, ²⁰⁸/²⁰⁴Pb = 38.77–39.58 chalcopyrite: ²⁰⁶Pb/²⁰⁴Pb = 18.67–19.38, ²⁰⁷/²⁰⁴Pb = 15.76–19.90, and ²⁰⁸/²⁰⁴Pb = 39.13–39.56) and oxide (scheelite: ²⁰⁶Pb/²⁰⁴Pb = 18.57–19.46, ²⁰⁷/²⁰⁴Pb = 15.71–15.77, ²⁰⁸/²⁰⁴Pb = 38.95–39.13) are different from those of the wall rock limestone (²⁰⁶Pb/²⁰⁴Pb = 18.34–18.60, ²⁰⁷/²⁰⁴Pb = 15.49–15.69, ²⁰⁸/²⁰⁴Pb = 38.57–38.88) and porphyries (²⁰⁶Pb/²⁰⁴Pb = 17.88–18.66, ²⁰⁷/²⁰⁴Pb = 15.59–15.69, ²⁰⁸/²⁰⁴Pb = 38.22–38.83), suggesting Pb²⁰⁶-, U²³⁸-, and Th ²³²-rich material are involved in the mineralization. The Sm–Nd isotopes of scheelite (ε_Nd(t) = − 6.1 to − 2.9), garnet (ε_Nd(t) = − 6.8 to − 6.1), and calcite (ε_Nd(t) = − 6.3) from W–Mo ores as well as calcite (ε_Nd(t) = − 5.4 to − 5.3) and scheelite (ε_Nd(t) = − 2.9) from the Cu ores demonstrate suggest more mantle-derived materials involved in the Cu mineralization.In the present study we conclude that two sources of ore-forming fluids were involved in production of the Huangshaping W–Mo–Pb–Zn–Cu deposit. One is associated with the granite porphyry magmas responsible for the W–Mo and then Pb–Zn mineralization during which its fluid evolved from magmatic immiscible to a magmatic–meteoritic mixing, and the other is derived from deep-rooted magma, which is related to Cu-related mineralization.     

Re–Os dating of sulphides from the Yushui Cu-polymetallic deposit in eastern Guangdong Province,South China

The Yushui Cu-polymetallic deposit, which is associated with Ag, Pb, and Zn, is located in the middle part of the Yongan–Meixian Late Paleozoic Hercynian depression. It was discovered in eastern Guangdong Province in the late 1980s and is one of the richest copper deposits in China with high-grade copper averaging 3.25% and locally reaching 50–60%. The main ore body is located along the unconformity between the Upper Carboniferous Hutian Group limestone and the Lower Carboniferous Zhongxin Formation quartz sandstone with a bedded and lenticular morphology. The ores exhibit massive textures dominated by chalcopyrite, bornite, chalcocite, pyrite, sphalerite, galena, and a trace amount of argentite. Although researchers began studying the Yushui deposit in the early 1990s, the ore genesis remains controversial because of the lack of precise mineralisation age constraints. In this study, direct Re–Os dating of Cu sulphides aided in facilitating a better understanding of the timing of formation of the Yushui deposit. This study is the first attempt to use the Re–Os isotopic system for directly dating chalcopyrite and bornite ores for the Yushui deposit. The contents of Re, common Os, ¹⁸⁷Re and ¹⁸⁷Os in nine sulphides are 1.68–219.35 ppb, 0.003–0.427 ppb, 1.05–137.31 ppb, and 0.045–0.734 ppb, respectively. The isotope data yielded an isochron age of 308 ± 15 Ma (mean square weighted deviates = 2.4) using the ⁸⁷Re/¹⁸⁸Os–¹⁸⁷Os/¹⁸⁸Os plot, which is interpreted to represent the age of formation for these sulphides, suggesting that the mineralisation age of the Yushui deposit is close to the age of the host rocks. The ¹⁸⁷Os/¹⁸⁸Os initial value obtained from the Re–Os isochron is 1.81 ± 0.34, which corresponds to the γOs value of + 1349. This value indicates that the ore-forming materials were derived from the crust without mixing with materials from the mantle, and that the Yushui massive sulphide deposit may be of sedimentary exhalative origin.     

Geochemical characteristics of pyrite in Duolanasayi gold deposit, Xinjiang

The Duolanasayi gold deposit, 60 km NW of Habahe County, Xinjiang Uygur Autonomous Region, is a mid-large-scale gold deposit controlled by brittle-ductile shearing, and superimposed by albitite veins and late-stage magma hydrothermal solutions. There are four types of pyrite, which are contained in the light metamorphosed rocks (limestone, siltstone), altered-mineralized rocks (chlorite-schist, altered albite-granite, mineralized phyllite), quartz veins and carbonatite veinlets. The pyrite is the most common ore mineral. The Au-barren pyrite is present mainly in a simple form and gold-bearing pyrite is present mainly in a composite form. From the top downwards, the pyrite varies in crystal form from {100} and {210} {100} to {210} {100} {111} to {100} {111}. Geochemical studies indicate that the molecular contents of pyrite range from Fe1.057S2 to Fe0.941S2. Gold positively correlates with Mn, Sr, Zn, Te, Pb, Ba and Ag. There are four groups of trace elements: Fe-Cu-Sr-Ag, Au-Te-Co, As-Pb-Zn and Mn-V-Ti-Ba-Ni-Cr in pyrite. The REE characteristics show that the total amount of REE (ΣREE) ranges from 32.35×10 -6 to 132.18×10 -6; LREE/HREE, 4.466-9.142; (La/Yb)N, 3.719-11.133; (Eu/Sm)N, 0.553-1.656; (Sm/Nd)N, 0.602-0.717; La/Yb, 6.26-18.75; δEu, 0.628-2.309; δCe, 0.308-0.816. Sulfur isotopic compositions (δ 34S=-2.46‰--7.02‰) suggest that the sulfur associated with gold mineralization was derived from the upper mantle or lower crust.     

Genesis of fahlore in the Tianbaoshan lead–zinc deposit,Sichuan Province,China: a scanning electron microscopy–energy dispersive spectroscopy study

The Tianbaoshan deposit, located in the southwestern part of the Yangtze Block, is a representative Pb–Zn deposit in the Sichuan–Yunnan–Guizhou Pb–Zn metallogenic province. The Pb–Zn orebodies are hosted in the upper Sinian Dengying Formation dolostone. The predominant minerals are sphalerite, galena, pyrite, chalcopyrite, quartz, and calcite with minor arsenopyrite, fahlore, and dolomite. The deposit is characterized by relatively strong Cu mineralization. However, the relationship between Pb–Zn and Cu mineralization is unknown. We analyzed the mineralogy and composition of fahlore, chalcopyrite, arsenopyrite, sphalerite, and galena using scanning electron microscopy–energy dispersive spectroscopy, with the aim of providing new evidence for the genesis of the Pb–Zn–(Cu) ore. The results show that the Cu ore in the deposit is dominated by chalcopyrite and fahlore, both of which formed before or during the Pb–Zn ore-forming stage. The fahlore showed dramatic compositional variation and was characterized by negative correlations between Ag and Cu, and between As and Sb, suggesting substitution of Ag for Cu, and that As and Sb substitute in the same site in the fahlore lattice. Based on backscattered electron images and composition, the fahlore was divided into two types. Type I fahlore crystallized early and is characterized by enrichment of Cu and depletion in Ag and Sb. Type II fahlore formed after Type I, and is rich in Ag and poor in Cu and As. Moreover, galena and fahlore are the host minerals of Ag. The variation of valence state with As host mineral—from fahlore to arsenopyrite—indicates the metallogenic environment changed from relatively oxidizing to reducing with a high pH. In the light of Gibbs energies of reciprocal reactions and isotherms for cation exchange, the composition of the fahlore implies its ore-forming temperature was lower than 220 °C, corresponding with typical Mississippi Valley-type (MVT) deposits. Based on the geologic character and geochemical data of this deposit, we suggest that the Tianbaoshan deposit belongs to the MVT deposit category.     

Petrologic and Geochemical Characteristics and Origin of Gusui Cherts,Guangdong Province,China

The characteristic structures of the Precambrian cherts from the Gusui section, Guangdong ,Chi-na, include bedded structure ,laminated structure ,massive structure and pseudobrecciated structure.The chert is characterized by consistently low abundance of TiO2,Al2O3 and most trace elements.Howevver ,it is enriched in Ba,As,Sb,Hg and Se.In Al-Fe-Mn ternary diagrams,it falls into the “hydrothermal field“ .Correspondence analysis and factor analysis show that many elements show up in the factor that represents the leaching of country rocks by hydrothermal solutions,and are the very characteristic element association fo the geochemically anomalous South China basement.Petrologic and geochemical evidence suggests a hydrothermal origin for the chert.The chert may have been formed in a Precambrian fift or an extension zone developed within the Yunkai marginal geosyncline, with a fault system linking it to an unknown heat source at depth.     

Stable isotope geochemistry and Re–Os ages of the Yinan gold deposit,Shandong Province,northeastern China

The Yinan gold deposit in the Luxi area of Shandong Province in northeastern China is a skarn-type ore deposit. In this article, we present results from sulphur, lead, carbon–oxygen, and helium–argon isotope chemistry to characterize the ore genesis and source features. We also present rhenium–osmium ages from molybdenite to evaluate the timing of ore formation. The δ³⁴S values of pyrite from the ore deposit range from 0.7‰ to 5.60‰ with a mean at 2.70‰, close to mantle and meteorite sulphur. Among Pb isotopes, ²⁰⁶Pb/²⁰⁴Pb values range from 18.375 to 18.436, ²⁰⁷Pb/²⁰⁴Pb values from 15.694 to 15.8, and ²⁰⁸Pb/²⁰⁴Pb values from 38.747 to 39.067. The δ¹³C values of calcite associated with the ores range from ?0.2‰ to ?0.5‰ and their δ¹⁸O values show variation from 9.4‰ to 12.6‰, suggesting a mixed fluid source. The ³He/⁴He and ⁴⁰Ar/³⁶Ar ratios of fluids trapped in pyrite are in the range of 0.27–1.11 Ra and 439.4–826, respectively, with calculated proportion of the mantle-derived He ranging from 3.25% to 14.03% and atmosphere argon ranging from 35.8% to 67.3%. The data suggest that the ore-forming fluids were derived from the crust and were mixed with a distinct contribution of mantle helium. The Re and Os values vary from 32 × 10^?6 to 93.02 × 10^?6 and from 0.01 × 10^?9 to 0.34 × 10^?9, respectively. The model ages of molybdenite range from 126.96 ± 1.82 Ma to 129.49 ± 2.04 Ma, with a weighted mean age of 128.08 ± 0.75 Ma and isochron age of 130.3 ± 3 Ma. These ages are close to the age of the associated quartz diorite porphyrite pluton, suggesting a close relationship between Cretaceous magmatism and metallogeny in NE China. A comparison of the Yinan gold deposit in the Luxi area with those of the Jiaodong area shows that the contrast in metallogenic features between the two are linked with the tectonic and geodynamic history.     

Geology,fluid inclusions,and geochemistry of the Zhazixi Sb–W deposit,Hunan, South China

The Zhazixi Sb–W deposit in the Xuefeng uplift, South China, exhibits a unique metal association of W and Sb, where the W orebodies are hosted by interlayer fractures and the Sb orebodies are contained within NW-trending faults. This study proposes that the W and Sb mineralization took place in two separate periods. The mineral paragenesis of the W mineralization reveals a mass of quartz, scheelite and minor calcite. The mineral assemblage of the Sb mineralization developed after W mineralization and consists of predominantly quartz and stibnite, and small amounts of native Sb, berthierite, chalcostibnite, pyrite, and chalcopyrite. Fluid inclusions in quartz and coexisting scheelite are dominated by two-phase, liquid-rich, aqueous inclusions at room temperature. Microthermometric studies suggest that ore-forming fluids for W mineralization are characterized by moderate temperatures (170–270 °C), low salinity (3–7 wt% NaCl equiv.), low density (0.75–0.95 g/cm³), and moderate to high pressure (57.2–99.7 MPa) and these fluids experienced a cooling and dilution evolution during W mineralization. Ore-forming fluids for Sb mineralization are epithermal types with low temperatures (150–230 °C), low salinity (4–6 wt% NaCl equiv.), moderate density (0.82–0.94 g/cm³), and high pressure (42.2–122.5 MPa) and these fluids display an evident decline in homogenization temperature during Sb mineralization. Laser Raman analyses of the vapor phase indicate that the ore-forming fluids for both W and Sb mineralization contain a small amount of CO₂.The ore-forming fluids for Sb mineralization are identified as predominantly originating from the continental crust, as suggested by the low ³He values (0.009 × 10⁻¹² cc.STP/g) and ³He/⁴He ratios (0.002–0.056 Ra) as well as high ³⁶Ar values (1.93 × 10⁻⁹ cc.STP/g) and ⁴⁰Ar/³⁶Ar ratios (909.5–2279.7). The source of S is identified to be the Neoproterozoic Wuqiangxi Formation, as traced by the δ³⁴S_V-CDT values of stibnite (3.1–9.4‰). The ²⁰⁸Pb/²⁰⁴Pb (37.643–40.222), ²⁰⁷Pb/²⁰⁴Pb (15.456–15.681), and ²⁰⁶Pb/²⁰⁴Pb (17.093–20.042) ratios suggest a mixture of lower crustal and supracrustal Pb sources.It is thus concluded that the ore genesis of the Zhazixi Sb–W deposit is related to the intracontinental orogeny during the early Mesozoic. Fluid mixing is considered to be the critical mechanism involved in W mineralization, whereas a fluid cooling process is responsible for Sb mineralization. Furthermore, the absence of Au is attributed to the low Σa_s content in Sb-mineralizing fluids.     

Geochemistry and geochronology of porphyries from the Beiya gold–polymetallic orefield,western Yunnan,China

The Beiya gold–polymetallic orefield, with gold reserves of 305 t, is one of the most representative porphyry-skarn orefields in the Jinshajiang–Ailaoshan Cu–Au ore belt within the Sanjiang region of southwest China. The orefield contains seven deposits: the Wandongshan, Hongnitang, Dashadi, Bijiashan, Weiganpo, Matouwan, and Bailiancun deposits. In this paper we report on the geochemistry and geochronology of porphyries associated with mineralization from the seven deposits. The results show that all the porphyries have similar geochemistry, with high alkalinity, high contents of SiO₂, Al₂O₃, K₂O, and Sr, high K₂O/Na₂O ratios, low MgO, Y, and Yb contents, enrichments in Ba, K, and Pb, depletions in P, Ti, Nb, and Ta, and non-evident to weak Eu depletions (δEu = 0.42–0.99). In the SiO₂ vs. Th/Ce diagram, the porphyry samples are distributed in the area of thickened lower crust, and in the Sr/Y vs. Y and La/Yb vs. Yb diagrams, the porphyries broadly followed the batch-melting trend of amphibolite containing up to 10% garnet. LA-MC-ICP-MS zircon U–Pb dating analysis suggests that the porphyries were emplaced between 34.62 ± 0.25 and 36.72 ± 0.25 Ma. They were coeval with lamprophyres (34 to 36 Ma) in the Beiya area and with potassic–ultrapotassic intrusive rocks (40 to 35 Ma) within the Jinshajiang–Ailaoshan magmatic belt, indicating possible genetic relation between these rock types. We suggest that the porphyries in the Beiya gold–polymetallic orefield were derived from the partial melting of a K-rich mafic source in the thickened lower crust, with the melting triggered by asthenospheric upwelling following the removal of lower lithospheric mantle.     

U–Pb zircon geochronology,geochemical, and Sr–Nd isotopic constraints on the age and origin of basaltic porphyries from western Liaoning Province,China

Basaltic porphyries from the northeast North China craton (NCC) provide an excellent opportunity to examine the nature of their mantle source and the secular evolution of the underlying mantle lithosphere. In addition, the study helps to constrain the age and the mechanism of NCC lithospheric destruction. In this paper, we report geochronological, geochemical, and Sr–Nd isotopic analyses of a suite of mafic lavas. Detailed laser ablation–inductively coupled plasma–mass spectrometry (LA–ICP–MS) zircon U–Pb dating yielded an age of 223.3 ± 1.1 million years, which we regard as representing the crystallization age of the basaltic porphyries. The bulk-rock analysed samples are enriched in both large ion lithophile elements (LILEs) (i.e. Ba, Sr, and Pb) and light rare earth elements (LREEs), but depleted in high field strong elements (HFSEs) (i.e. Nb, Ta, Zr, Hf, and Ti) and heavy rare earth elements (HREEs), without significant Eu anomalies (Eu/Eu*?= 089–0.98). The basaltic porphyries have undergone low degrees (～5%) of partial melting of a garnet-bearing lherzolite mantle. The rocks display very uniform (⁸⁷Sr/⁸⁶Sr) _i (0.70557–0.70583) and negative ?_Nd (t) values (–11.9 to –10.1). These features indicate that the western Liaoning basaltic porphyries were derived from a common enriched lithosphere mantle that had previously been metasomatized by fluids related to subduction of Palaeo-Asian sedimentary units. However, the mafic melts were not affected to a significant degree by crustal contamination. Based on earlier studies, these findings provide new evidence that the northeast margin of the NCC had undergone a phase of post-orogenic extensional tectonics during the Middle Triassic. Furthermore, lithospheric thinning occurring across the northern NCC might have been initiated during Early Triassic times and was likely controlled by the final closure of the Palaeo-Asian Ocean, as well as the collision of Mongolian arc terrenes with the NCC.