Indium Mineralization in Copper–Tin Stratiform Skarn Ores at the Saishitang–Rilonggou Ore Field,Qinghai, Northwest China

The Saishitang–Rilonggou Ore Field (SROF), which includes the Saishitang, Tongyugou, and Rilonggou ore deposits as well as other scattered occurrences, is located in the Elashan region in Qinghai Province, and is a significant Cu–Sn ore field in NW China. These ores are hosted in stratiform skarn deposits with the main metals being Cu and Sn, as well as Zn, Pb, Au, Ag, and trace elements (e.g. Ga, Ge, Se, and In). Bulk‐rock geochemical analyses of 50 ore samples from the three deposits show that In contents in the Saishitang deposit range from 0.03 to 39 ppm (average 12.7 ppm, n = 19), with 1000 In/Zn values that vary from >0.01 to 29.83 (average 4.29). Indium contents in the Tongyugou deposit vary from 7.51 to 131 ppm (average 28.37 ppm, n = 13), with 1000 In/Zn values from 0.74 to 48 (average 17.55). Finally, indium contents in the Rilonggou deposit vary from 0.73 to 120 ppm (average 36.15 ppm, n = 18), with 1000 In/Zn values from 0.33 to 47 (average 8.52). Indium is hosted mainly in sphalerite, while some other In‐bearing minerals (e.g., roquesite, stannoidite, and stannite) are present locally within the ore field. Roquesite, which replace or fill bornite, occurs in bornite‐rich ores in the Saishitang deposit. This is the first reported Chinese locality of roquesite. Based on previously reported Zn resources, a total of 136 tons of In is calculated to be hosted in the SROF, with 30, 66, and 40 tons of In attributed to the Saishitang, Tongyugou, and Rilonggou deposits, respectively. The differences in indium contents among the deposits and their respective geological histories and characteristics suggest that the origin of indium relates to volcanogenic metallogenesis in an early Permian volcano‐sedimentary basin. Based on the evaluation of In resources, future mining operations should include the recovery of indium in the Tongyugou and Rilonggou deposits.     

The Crater Mountain Deposit,Papua New Guinea: Porphyry‐related Au–Te System

Ore mineralization and wall rock alteration of Crater Mountain gold deposit, Papua New Guinea, were investigated using ore and host rock samples from drill holes for ore and alteration mineralogical study. The host rocks of the deposit are quartz‐feldspar porphyry, feldspar‐hornblende porphyry, andesitic volcanics and pyroclastics, and basaltic‐andesitic tuff. The main ore minerals are pyrite, sphalerite, galena, chalcopyrite and moderate amounts of tetrahedrite, tennantite, pyrrhotite, bornite and enargite. Small amounts of enargite, tetradymite, altaite, heyrovskyite, bismuthinite, bornite, idaite, cubanite, native gold, CuPbS₂, an unidentified Bi‐Te‐S mineral and argentopyrite occur as inclusions mainly in pyrite veins and grains. Native gold occurs significantly in the As‐rich pyrite veins in volcanic units, and coexists with Bi‐Te‐S mineral species and rarely with chalcopyrite and cubanite relics. Four mineralization stages were recognized based on the observations of ore textures. Stage I is characterized by quartz‐sericite‐calcite alteration with trace pyrite and chalcopyrite in the monomict diatreme breccias; Stage II is defined by the crystallization of pyrite and by weak quartz‐chlorite‐sericite‐calcite alteration; Stage III is a major ore formation episode where sulfides deposited as disseminated grains and veins that host native gold, and is divided into three sub‐stages; Stage IV is characterized by predominant carbonitization. Gold mineralization occurred in the sub‐stages 2 and 3 in Stage III. The fS₂ is considered to have decreased from ～10^?2 to 10^?14 atm with decreasing temperature of fluid.     

Geochemical dispersion about the Western Tharsis Cu–Au deposit, Mt Lyell, Tasmania

The Western Tharsis disseminated Cu–Au orebody, which occurs within the Cambrian Mt Read Volcanics of Western Tasmania, is surrounded by a pyritic halo that extends 100–200 m stratigraphically above and below the ore zone. Although this halo extends laterally along the same stratigraphic position to the south, it probably closes off to the north based on limited surface and drill hole data. The ore zone is characterized by extreme enrichment (the enrichments and depletions referred to herein are relative to background; these have not been established using mass balance techniques) in As, Bi, Ce, Cu, Mo, Ni, S and Se; with the exception of Mo, these elements are also enriched, but at a much lower level, in the pyrite halo.Pronounced depletion in K, Cs and Mg occurs in 20–30 m wide stratiform zones that flank the orebody on both sides within the pyritic halo. These anomalies and depletions in Be, Ga, Rb, Y, MREE and HREE are associated with a pyrophyllite-bearing alteration zone that wraps around the main pyrite–chalcopyrite-bearing ore zone. This zone is also characterized by positive Eu anomalies which persist up to 150 m both into the hanging wall and footwall of the orebody. The depletion of these elements is consistent with the advanced argillic alteration assemblage developed about acid-sulfate Cu–Au deposits.The pyrite halo is surrounded by a peripheral carbonate halo which is highly enriched in C, CaO and MnO, and weakly enriched in Zn and Tl. Zinc and Tl are most enriched in the upper 100–150 m of the stratigraphically lower halo. In the stratigraphically upper halo, Zn and Tl values are anomalously high but erratic.Barium and Sr enrichment, although mainly restricted to the pyrite halo, extends into the stratigraphically lower carbonate halo by up to 100 m. A Na depletion anomaly extends from 150 m below the orebody and to at least the Owen contact (i.e. ≥400 m)in the hanging wall.The dispersion patterns observed at Western Tharsis are quite unlike those of Zn–Pb-rich volcanic-hosted massive sulfide (VHMS) deposits in western Tasmania. Rather, the dispersion patterns observed at Western Tharsis are more akin to those surrounding porphyry Cu deposits and related acid-sulfate Cu–Au deposits.     

Sm–Nd and Ar–Ar Isotopic Dating of the Nuri Cu–W–Mo Deposit in the Southern Gangdese,Tibet: Implications for the Porphyry‐Skarn Metallogenic System and Metallogenetic Epochs of the Eastern Gangdese

The Nuri Cu–W–Mo deposit is a large newly explored deposit located at the southern margin of the Gangdese metallogenic belt. There are skarn and porphyry mineralizations in the deposit, but the formation age of the skarn and the relationship between the skarn and porphyry mineralizations are controversial. Constraints on the precise chronology are of fundamental importance for understanding the ore genesis of the Nuri deposit. To determine the formation age of the skarn, we chose garnets and whole rock skarn samples for Sm–Nd dating. We also selected biotite associated with potassic alteration for Ar–Ar dating to confirm the ore formation age of the porphyry mineralizations. The Sm–Nd ages of the skarn are 25.73 ± 0.92 – 25.2 ± 3.9 Ma, and the age of the potassic alteration is 24.37 ± 0.32 Ma. The results indicate that the skarn and porphyry mineralization are coeval and belong to a unified magmatic hydrothermal system. Combined with a previous molybdenite Re–Os age, we think that the hydrothermal activity of the Nuri deposit lasted for 1.2 – 2.1 Myr, which indicates that the mineralization formed rapidly. The chronologic results indicate that the Nuri deposit formed in the period of transformation from compression to extension in the late collisional stage of the collision between the Indian and Eurasian continents.     

Two Cu–Co sulfide phases and contrasting fluid systems in the Katanga Copperbelt, Democratic Republic of Congo

The Katanga Copperbelt is the Congolese part of the well-known Central African Copperbelt, the largest sediment-hosted stratiform Cu–Co province on Earth. Petrographic examination of borehole samples from the Kamoto and Luiswishi mines in the Katanga Copperbelt recognized two generations of hypogene Cu–Co sulfides and associated gangue minerals (dolomite and quartz). The first generation is characterized by fine-grained Cu–Co sulfides and quartz replacing dolomite. The second generation is paragenetically later and characterized by coarse-grained Cu–Co sulfides and quartz overgrown and partly replaced by dolomite. Fluid inclusion microthermometric data were collected from two different types of fluid inclusions: type-I fluid inclusions (liquid + vapor) in the quartz of the first generation and type-II fluid inclusions (liquid + vapor + halite) in the quartz of the second generation. The microthermometric analyses indicate that the fluids represented by type-I and type-II fluid inclusions had very different temperatures and salinities and were not in thermal equilibrium with the host rock.Petrographic and microthermometric data indicate the presence of at least two main hypogene Cu–Co sulfide phases in the Katanga Copperbelt. The first is an early diagenetic typical stratiform phase, which produced fine-grained sulfides that are disseminated in the host rock and frequently concentrated in nodules and lenticular layers. This phase is related to a hydrothermal fluid with a moderate temperature (115 to 220 °C, or less if reequilibration of inclusions has occurred) and salinity (11.3 to 20.9 wt.% NaCl equiv.). The second hypogene Cu–Co phase produced syn-orogenic coarse-grained sulfides, which also occur disseminated in the host rock but mainly concentrated in a distinct type of stratiform nodules and layers and in stratabound veins and tectonic breccia cement. This second phase is related to a hydrothermal fluid with high temperature (270 to 385 °C) and salinity (35 to 45.5 wt.% NaCl equiv.).A review of available microthermometric and ore geochronological data of the Copperbelt in both the Democratic Republic of Congo and Zambia supports the regional presence of the two Cu–Co phases proposed in our study. Future geochemical analyses in the Copperbelt should take into account the presence of, at least, these two Cu–Co phases, their contrasting fluid systems and the possible overprint of the first phase by the second one.     

Fluid Inclusion Studies of Comb Quartz and Stibnite at the Hishikari Au–Ag Epithermal Deposit,Japan

Fluid inclusion microthermometry was conducted on late‐stage barren comb quartz and the latest stibnite at the Hishikari deposit to characterize the hydrothermal activity responsible for vein formation. Eight fluid inclusion assemblages (i.e. fluid inclusions trapped at the same time, ‘FIAs’) were studied to determine the formation fluid temperatures and salinities for the comb quartz in the Shosen No. 2 vein, Sanjin ore zone, and the stibnite in the Seisen No. 1–1 vein, Yamada ore zone. The average homogenization temperatures (the formation temperatures) of the seven FIAs from the comb quartz were between 207 and 230°C, while the average homogenization temperature (the formation temperature) of an FIA from the stibnite was 113°C. The measured fluid salinities of the seven FIAs from the comb quartz were low, ranging between 0.0 and 1.1 wt% NaCl equiv., indicating that dilute fluids were responsible for the comb quartz formation. By comparison with previous microthermometric data, the formation temperatures of the studied comb quartz were higher than those of columnar adularia and comb quartz at most other veins (generally around 200°C) but were similar to those of columnar adularia at Keisen veins (230°C) in the same ore zone. The higher formation temperatures both in the Shosen and the Keisen veins in the Sanjin ore zone indicate that the fractures corresponding to the vein system at the Sanjin ore zone were main conduits for hot ascending fluids. The low formation temperature of stibnite in the latest stage (113°C) indicates that stibnite precipitation occurred during a waning stage of hydrothermal activity. Combined with previous thermodynamic data on antimony solubilities, the large discrepancy between the formation temperature of the comb quartz (200–230°C) and that of the stibnite suggests that the stibnite may have precipitated as a result of a drastic cooling of the hydrothermal system.     

A Study on the Mineralization of the Woxi Au–Sb–W Deposit,Western Hunan,China

The Woxi Au–Sb–W deposit in the western Hunan Province, China, is of hydrothermal vein type characterized by a rare mineral assemblage of stibnite, scheelite and native gold, of which gold fineness ranges from 998.6 to 1000. The mineralization sequence observed in the deposit is, from early to late, coarse‐grained pyrite – scheelite – stibnite – Pb–Sb–S minerals – sphalerite (+ cubanite) – fine‐grained pyrite. Native gold may have precipitated with scheelte. Microthermometric and LA–ICP–MS analyses of fluid inclusions in scheelite, quartz associated with scheelite and stibnite and barren quartz clarified that there may be at least three types of hydrothermal fluids during the vein formation in the Woxi deposit. Scheelite and native gold precipitated from the fluid of high temperature and salinity with high concentrations of metal elements, followed by stibnite precipitation. The later fluid of the highest temperature and salinity with low concentrations of the elements yielded the sphalerite mineralization. The latest fluid of low temperature and salinity with low concentrations of the elements is observed mainly in barren quartz. The remarkably high Au/Ag concentration ratios determined in the fluid inclusions in scheelite might be the reason for the extremely high gold fineness of native gold.     

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

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

Geologic, Fluid Inclusion and Stable Isotope Constraints on Mechanisms of Ore Deposition at the Datuanshan Copper Deposit, Middle–Lower Yangtze Valley, Eastern China

The Datuanshan deposit is one of the largest and most representative stratabound copper deposits in the Tongling area,the largest ore district in the Middle-Lower Yangtze River metallogenic belt.The location of the orebodies is controlled by the interlayer-slipping faults between the Triassic and Permian strata,and all the orebodies are distributed in stratiform shape around the Mesozoic quartz monzodiorite dikes.Based on field evidence and petrographic observations,four mineralization stages in the Datuanshan deposit have been identified:the skarn,early quartz-sulfide,late quartzsulfide and carbonate stages.Chalcopytite is the main copper mineral and mainly formed at the late quartz-sulfide stage.Fluid inclusions at different stages were studied for petrography,microthermometry,laser Raman spectrometry and stable isotopes.Four types of fluid inclusions,including three-phase fluid inclusions(type 1),liquid-rich fluid inclusions(type 2),vapour-rich fluid inclusions(type 3) and pure vapour fluid inclusions(type 4),were observed.The minerals from the skarn,early and late quartz-sulfide stages contain all fluid inclusion types,but only type 2 fluid inclusions were observed at the carbonate stage.Petrographic observations suggest that most of the inclusions studied in this paper are likely primary.The coexistence of different types of fluid inclusions with contrasting homogenization characteristics(to the liquid and vapour phase,respectively) and similar homogenization temperatures(the modes are 440-480℃,380-400℃ and 280-320℃ for the skarn,early and late quartz-sulfide stages,respectively) in the first three stages,strongly suggests that three episodes of fluid boiling occurred during these stages,which is supported by the hydrogen isotope data.Laser Raman spectra identified CH_4 at the skarn and early quartz-sulfide stages.Combined with other geological features,the early ore-forming fluids were inferred to be under a relatively reduced environment.The CO_2 component has been identified at the late quartz-sulfide and carbonate stages,indicating that the late ore-forming fluids were under a relatively oxidized environment,probably as a result of inflow of and mixing with meteoric water.In addition,microthermometric results of fluid inclusions and H-O isotope data mdicate that the ore forming fluids were dominated by magmatic water in the early stages(skarn and early quartz-sulfide stages) and mixed with meteoric water in the late stages(late quartz-sulfide and carbonate stages).The evidence listed above suggests that the chalcopyrite deposition in the Datuanshan deposit probably resulted from the combination of multiepisode fluid boiling and mixing of magmatic and meteoric water.     

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

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

A Low‐Sulfidation Epithermal Mineralization in the River Reef Zone,the Poboya Prospect,Central Sulawesi,Indonesia: Vein Textures,Ore Mineralogy,and Fluid Inclusions

The Poboya Prospect lies along the North Northwest ‐ South Southeast Palu‐Koro Fault Zone in the central part of the West Sulawesi Arc. The geology of the area consists of the Palu Metamorphic Complex overlain by the Paleogene‐Neogene Tinombo Formation of volcanosedimentary rocks, the Celebes Molasse sediment, and Late Cenozoic granitic rocks. Petrography, scanning electron microscope with energy‐dispersive spectrometry (SEM‐EDS), electron probe microanalyzer (EPMA), and fluid inclusion microthermometry were carried out to examine vein textures, ore mineralogy, and characteristics of the ore‐forming fluid responsible for mineralization in the River Reef Zone, the Poboya Prospect. Textures of quartz‐carbonate veins in the River Reef Zone include massive micro‐comb, moss, colloform, crustiform, mosaic, feathery, flamboyant, lattice bladed, ghost bladed, parallel bladed, and saccharoidal textures representing primary growth, recrystallization, and replacement. The homogenization temperature and fluid salinity are 240–250°C and 0.3–0.7 wt% NaCl eq., respectively. Ore minerals precipitated in the early stage consist of electrum, naumannite‐aguilarite, chalcopyrite, pyrite, marcasite, sphalerite, and pyrrhotite. Apart from pyrrhotite, these ore minerals were also precipitated in the late stage along with selenopolybasite, freibergite, argyrodite, pyrargyrite, and galena. Selenium more preferably occurs as the crystallographic replacement of sulfur in naumannite‐aguilarite, argyrodite, pyrargyrite, selenopolybasite, and freibergite instead of as independent selenide minerals. The low‐sulfidation epithermal deposit in the River Reef Zone, the Poboya Prospect, illustrates the potential of the West Sulawesi Arc, particularly along the Palu‐Koro Fault Zone, to host epithermal gold mineralization.     

Rb–Sr Dating of Gold‐Bearing Pyrite in the Jinchang Porphyry Cu–Au Deposit,Heilongjiang Province,NE China

The Jinchang Cu–Au deposit in Heilongjiang Province, NE China, is located in the easternmost part of the Central Asian Orogenic Belt. Rb–Sr analyses of auriferous pyrite from the deposit yielded an isochron age of 113.7 ±2.5 Ma, consistent with previously reported Re–Os ages. Both sets of ages represent the timing of Cu–Au mineralization because (i) the pyrite was separated from quartz–sulfide veins of the mineralization stage in granite porphyry; (ii) fluid inclusions have relatively high Rb, Sr, and Os content, allowing precise measurement; (iii) there are no other mineral inclusions or secondary fluids in pyrite to disturb the Rb–Sr or Re–Os decay systems; and (iv) the closure temperatures of the two decay systems are ≥500°C (compared with the homogenization temperatures of fluid inclusions of 230–510°C). It is proposed that ore‐forming components were derived from mantle–crust mixing, with ore‐forming fluids being mainly exsolved from magmas with minor amounts of meteoric water. The age of mineralization at Jinchang and in the adjacent regions, combined with the tectonic evolution of the northeast China epicontinental region, indicates that the formation of the Jinchang porphyry Cu–Au deposit was associated with Early Cretaceous subduction of the paleo‐Pacific Plate.     

Porphyry Cu–Au and associated polymetallic Fe–Cu–Au deposits in the Beiya Area, western Yunnan Province, south China

The Alkaline porphyries in the Beiya area are located east of the Jinshajiang suture, as part of a Cenozoic alkali-rich porphyry belt in western Yunnan. The main rock types include quartz-albite porphyry, quartz-K-feldspar porphyry and biotite–K-feldspar porphyry. These porphyries are characterised by high alkalinity [(K₂O + Na₂O)% > 10%], high silica (SiO₂% > 65%), high Sr (> 400 ppm) and ⁸⁷Sr/⁸⁶Sr (> 0.706)] ratio and were intruded at 65.5 Ma, between 25.5 to 32.5 Ma, and about 3.8 Ma, respectively. There are five main types of mineral deposits in the Beiya area: (1) porphyry Cu–Au deposits, (2) magmatic Fe–Au deposits, (3) sedimentary polymetallic deposits, (4) polymetallic skarn deposits, and (5) palaeoplacers associated with karsts. The porphyry Cu–Au and polymetallic skarn deposits are associated with quartz–albite porphyry bodies. The Fe–Au and polymetallic sedimentary deposits are part of an ore-forming system that produced considerable Au in the Beiya area, and are characterised by low concentrations of La, Ti, and Co, and high concentrations of Y, Yb, and Sc.The Cenozoic porphyries in western Yunnan display increased alkalinity away from the Triassic Jinshajiang suture. Distribution of both the porphyries and sedimentary deposits in the Beiya area are interpreted to be related to partial melting in a disjointed region between upper mantle lithosphere of the Yangtze Plate and Gondwana continent, and lie within a shear zone between buried Palaeo-Tethyan oceanic lithosphere and upper mantle lithosphere, caused by the subduction and collision of India and Asia.     

Potassium–Argon Ages of the Epithermal Gold–Silver Mineralization in the Haenam–Jindo Area,Southwestern Korea

The Haenam–Jindo area, located on the southwestern margin of the Korean Peninsula, was the site of vigorous volcanic activity during the Late Cretaceous and Early Tertiary periods. Large parts of the area record strong hydrothermal alteration, and there exist many clay–alunite and gold–silver deposits. We undertook potassium–argon (K–Ar) age dating of five mineral samples (including adularia, sericite and alunite) from the Eunsan, Moisan and Gasado epithermal gold–silver deposits in this area. The purities of the samples were confirmed by X‐ray diffraction analysis. The K–Ar ages of adularia from the Eunsan deposit and adularia and sericite from the Moisan deposit (related to gold–silver mineralization) are 75.0 ± 1.6, 74.7 ± 1.6 and 75.1 ± 1.6 Ma, respectively. The similarity of these ages, combined with the close proximity and similar geochemical characteristics of the deposits, indicates that the mineralization occurred as part of a single hydrothermal system. The K–Ar ages of alunite at the surface and adularia at depth within the Gasado deposit are 82.2 ± 1.9 and 70.7 ± 1.9 Ma, respectively, revealing that the clay–alunite and gold–silver mineralization formed at different ages. K–Ar age data indicate that the gold–silver mineralization in this area occurred mainly at 75–70 Ma, resulting from hydrothermal activity in the Haenam–Jindo area (82–70 Ma). This is the first time that the mineralization of precious metals in Korea has been identified during this period.     

Genesis of the Weiquan Ag–Polymetallic Deposit in East Tianshan, China: Evidence from Zircon U–Pb Geochronology and C–H–O–S–Pb Isotope Systematics

The Weiquan Ag-polymetallic deposit is located on the southern margin of the Central Asian Orogenic Belt and in the western segment of the Aqishan-Yamansu arc belt in East Tianshan,northwestern China. Its orebodies, controlled by faults, occur in the lower Carboniferous volcanosedimentary rocks of the Yamansu Formation as irregular veins and lenses. Four stages of mineralization have been recognized on the basis of mineral assemblages, ore fabrics, and crosscutting relationships among the ore veins. Stage I is the skarn stage(garnet + pyroxene), Stage Ⅱ is the retrograde alteration stage(epidote + chlorite + magnetite ± hematite 士 actinolite ± quartz),Stage Ⅲ is the sulfide stage(Ag and Bi minerals + pyrite + chalcopyrite + galena + sphalerite + quartz ± calcite ± tetrahedrite),and Stage IV is the carbonate stage(quartz + calcite ± pyrite). Skarnization,silicification, carbonatization,epidotization,chloritization, sericitization, and actinolitization are the principal types of hydrothermal alteration. LAICP-MS U-Pb dating yielded ages of 326.5±4.5 and 298.5±1.5 Ma for zircons from the tuff and diorite porphyry, respectively. Given that the tuff is wall rock and that the orebodies are cut by a late diorite porphyry dike, the ages of the tuff and the diorite porphyry provide lower and upper time limits on the age of ore formation. The δ~(13)C values of the calcite samples range from-2.5‰ to 2.3‰, the δ~(18)O_(H2 O) and δD_(VSMOW) values of the sulfide stage(Stage Ⅲ) vary from 1.1‰ to 5.2‰ and-111.7‰ to-66.1‰, respectively,and the δ~(13)C, δ~(18)O_(H2 O) and δD_(V-SMOW) values of calcite in one Stage IV sample are 1.5‰,-0.3‰, and-115.6‰, respectively. Carbon, hydrogen, and oxygen isotopic compositions indicate that the ore-forming fluids evolved gradually from magmatic to meteoric sources. The δ~(34)S_(V-CDT) values of the sulfides have a large range from-6.9‰ to 1.4‰, with an average of-2.2‰, indicating a magmatic source, possibly with sedimentary contributions. The ~(206)Pb/~(204)Pb, ~(207)Pb/~(204)Pb, and ~(208)Pb/~(204)Pb ratios of the sulfides are 17.9848-18.2785,15.5188-15.6536, and 37.8125-38.4650, respectively, and one whole-rock sample at Weiquan yields~(206)Pb/~(204)Pb,~(207)Pb/~(204)Pb, and ~(208)Pb/~(204)Pb ratios of 18.2060, 15.5674, and 38.0511,respectively. Lead isotopic systems suggest that the ore-forming materials of the Weiquan deposit were derived from a mixed source involving mantle and crustal components. Based on geological features, zircon U-Pb dating, and C-H-OS-Pb isotopic data, it can be concluded that the Weiquan polymetallic deposit is a skarn type that formed in a tectonic setting spanning a period from subduction to post-collision. The ore materials were sourced from magmatic ore-forming fluids that mixed with components derived from host rocks during their ascent, and a gradual mixing with meteoric water took place in the later stages.     

Geochemistry,and zircon U–Pb and molybdenite Re–Os geochronology of Jilongshan Cu–Au deposit,southeastern Hubei Province,China

The Jilongshan skarn Cu–Au deposit is located at the Jiurui ore cluster region in the southwestern part of the Middle–Lower Yangtze River valley metallogenic belt. The region is characterized by NW‐, NNW‐ and EW‐trending faults and the mineralization occurs at the contact of lower Triassic carbonate rocks and Jurassic granodiorite porphyry intrusions. The intrusives are characterized by SiO₂, K₂O, and Na₂O concentrations ranging from 61.66 to 67.8 wt.%, 3.29 to 5.65 wt.%, and 2.83 to 3.9 wt.%, respectively. Their A/CNK (A/CNK = n(Al₂O₃)/[n(CaO) + n(Na₂O) + n(K₂O)]) ratio, δEu, and δCe vary from 0.77 to 1.17, 0.86 to 1, and 0.88 to 0.96, respectively. The rocks show enrichment in light rare earth elements ((La/Yb)_N = 7.61–12.94) and large ion lithophile elements (LILE), and depletion in high field strength elements (HFSE), such as Zr, Ti. They also display a peraluminous, high‐K calc‐alkaline signature typical of intrusives associated with skarn and porphyry Cu–Au–Mo polymetallic deposits. Laser ablation inductively coupled plasma spectrometry (LA‐ICP‐MS) zircon U–Pb age indicates that the granodiorite porphyry formed at 151.75 ± 0.70 Ma. A few inherited zircons with older ages (677 ± 10 Ma, 848 ± 11 Ma, 2645 ± 38 Ma, and 3411 ± 36 Ma) suggest the existence of an Archaean basement beneath the Middle–Lower Yangtze River region. The temperature of crystallization of the porphyry estimated from zircon thermometer ranges from 744.3 °C to 751.5 °C, and 634.04 °C to 823.8 °C. Molybdenite Re–Os dating shows that the Jilongshan deposit formed at 150.79 ± 0.82 Ma. The metallogeny and magmatism are correlated to mantle–crust interaction, associated with the subduction of the Pacific Plate from the east. Copyright © 2013 John Wiley & Sons, Ltd.     

Noble Gas and Stable Isotopic Constraints on the Origin of the Ag–Cu Polymetallic Ore Deposits in the Baiyangping Area,Yunnan Province,SW China

The Lanping basin, Yunnan province, SW China, is located at the juncture of the Eurasian and Indian Plates in the eastern part of the Tibetan Plateau. The Lanping basin, in the Sanjiang Tethyan metallogenic province, is a significant Cu–Ag–Zn–Pb mineralized belt in China that includes the largest sandstone‐hosted Zn–Pb deposit in the world, the Jinding deposit, as well as several Ag–Cu deposits (the Baiyangping and Jinman deposits). These deposits, with total reserves of over 16.0 Mt Pb + Zn, 0.6 Mt Cu, and 7,000 t Ag, are mainly hosted in Meso‐Cenozoic clastic rocks and are dominantly controlled by two Cenozoic thrust systems developed in the western and eastern segments of the basin. The Baiyangping, Babaoshan, and Hetaoqing ore deposits are representative of the epithermal base metal deposits in the Lanping basin. The microthermometric data show that the ore‐forming fluids for these deposits were low temperature (110–180 °C) and had bimodal distribution of salinity at moderate and mid to high salinities (approximately 2–8 wt.% and 18–26 wt.% NaCl equivalent). The C and O isotope data indicate that the ore‐forming fluids were related to hot basin brines. We present new He and Ar isotope data on volatiles released from fluid inclusions contained in sulfides and in barite in these three deposits. ³He/⁴He ratios of the ore‐forming fluids are 0.01 to 0.14 R/Ra with a mean of 0.07 Ra (where R is the ³He/⁴He ratio and Ra is the ratio for atmospheric helium). This mean value is intermediate to typical ³He/⁴He ratios for the crust (R/Ra = 0.01 to 0.05) and the ratio for air‐saturated water (R/Ra = 1). The mean ratio is also significantly lower than the ratios found for mantle‐derived fluids (R/Ra = 6 to 9). The ⁴⁰Ar/³⁶Ar ratios of the ore‐forming fluids range from 298 to 382 with a mean of 323. This value is slightly higher than that for the air‐saturated water (295.5). The ³He/⁴He ratios of fluids from the fluid inclusions imply that the ore‐forming fluid for the Baiyangping, Babaoshan, and Hetaoqing deposits was derived from the crust and that any mantle‐derived He was negligible. The content of the radiogenic Ar ranges between 0.2 to 20.4%, and the proportion of air‐derived ⁴⁰Ar averages 94.1%. This indicates that atmospheric Ar was important in the formation of these deposits but that some radiogenic ⁴⁰Ar was derived from crustal rocks. Based on these observations coupled with other geochemical evidence, we suggest that the ore‐forming fluids responsible for the formation of the Ag–Cu–Pb–Zn polymetallic ore deposits in the Baiyangping area of the Lanping basin were mainly derived from crustal fluids. The fluids may have mixed with some amount of air‐saturated water, but there was no significant involvement of mantle‐derived fluids.     

Genesis of the Xuebaoding W–Sn–Be Crystal Deposits in Southwest China: Evidence from Fluid Inclusions,Stable Isotopes and Ore Elements

The Xuebaoding crystal deposit, located in northern Longmenshan, Sichuan Province, China, is well known for producing coarse‐grained crystals of scheelite, beryl, cassiterite, fluorite and other minerals. The orebody occurs between the Pankou and Pukouling granites, and a typical ore vein is divided into three parts: muscovite and beryl within granite (Part I); beryl, cassiterite and muscovite in the host transition from granite to marble (Part II); and the main mineralization part, an assemblage of beryl, cassiterite, scheelite, fluorite, apatite and needle‐like tourmaline within marble (Part III). No evidence of crosscutting or overlapping of these ore veins by others suggests that the orebody was formed by single fluid activity. The contents of Be, W, Sn, Li, Cs, Rb, B, and F in the Pankou and Pukouling granites are similar to those of the granites that host Nanling W–Sn deposits. The calculated isotopic compositions of beryl, scheelite and cassiterite (δD, ?69.3‰ to ?107.2‰ and δ¹⁸O_H2O, 8.2‰ to 15.0‰) indicate that the ore‐forming fluids were mainly composed of magmatic water with minor meteoric water and CO₂ derived from decarbonation of marble. Primary fluid inclusions are CO₂? CH₄+ H₂O ± CO₂ (vapor), with or without clathrates and halites. We estimate the fluid trapping condition at T = 220 to 360°C and P > 0.9 kbar. Fluid inclusions are rich in H₂O, F^‐ and Cl^‐. Evidence for fluid‐phase immiscibility during mineralization includes variable L/V ratios in the inclusions and inclusions containing different phase proportions. Fluid immiscibility may have been induced by the pressure released by extension joints, thereby facilitating the mineralization found in Part III. Based on the geochemical data, geological occurrence, and fluid inclusion studies, we hypothesize that the coarse‐grained crystals were formed by: (i) the high content of ore elements and volatile elements such as F in ore‐forming fluids; (ii) occurrence of fluid immiscibility and Ca‐bearing minerals after wall rock transition from granite to marble making the ore elements deposit completely; (iii) pure host marble as host rock without impure elements such as Fe; and (iv) sufficient space in ore veins to allow growth.     

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

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

Preliminary mineralogical and petrological study of the Ortosa Au–Bi–Te ore deposit: a reduced gold skarn in the northern part of the Rio Narcea Gold Belt, Asturias, Spain

The Ortosa deposit (NW Spain) in the northern part of the Rio Narcea Gold Belt (RNGB) is located in the Cantabrian Zone of the Iberian Massif. This zone corresponds to the westernmost exposure of the European Hercynides. The deposit is hosted by marine shales, siltstones, calcareous siltstones and interbedded sandy limestones of the upper part of the Silurian Furada Formation. These rocks are intruded by a main stock and numerous sills and dikes consisting of a reduced, ilmenite-bearing quartz-monzodiorite (Ortosa intrusion). Skarn metasomatism and associated gold mineralization overprinted these sedimentary and igneous rocks, forming endo- and exoskarns.The earliest stage of alteration involved potassium metasomatism from which metasomatic biotite developed in the hornfels around the intrusion. In the endoskarn, the first metasomatic mineral to form is actinolite. Subsequently, quartz, pyroxene (Hd_30–45), and sulfides (mainly arsenopyrite and pyrrhotite) formed, followed by a second generation of amphibole (ferroactinolite and ferrohornblende). The exoskarn is a pyroxene-garnet skarn, which is often banded. The prograde minerals are pyroxene (Hd_10–30) and grossular garnet. The retrograde mineralogy consists of hedenbergite-rich pyroxene (Hd_50–87), amphibole (ferroactinolite–ferrohornblende), and the metallic minerals with minor fluorapatite, K-feldspar, albite, epidote–clinozoisite, vesuvianite and calcite. A final stage of retrograde alteration is characterized by calcite, quartz, and chlorite.Pyrrhotite and arsenopyrite are the more abundant metallic minerals, and löllingite, chalcopyrite, pyrite and sphalerite are present in smaller amounts. The gold occurs as native gold and maldonite, and is accompanied by hedleyite, native bismuth, and bismuthinite. These Au–Bi–Te mineral assemblages occupy cavities and fractures in the arsenopyrite or in the pyrrhotite.Estimated physiochemical conditions of formation based on the composition and stability fields of major calc-silicate and sulfide minerals indicate that the hedenbergite-rich pyroxene and the earliest sulfides (löllingite–pyrrhotite–arsenopyrite) crystallized at temperatures between 470 and 535°C at low log fS₂ between −10 and −6.5 and low log fO₂ of −22. The Ortosa skarns can be included in the reduced gold skarn subtype defined by Meinert (Mineralogical Association of Canada, Quebec city, Que., Canada, 1998, 26,359–414 ).