Involvement Of Meteoric Water Research Articles

Genesis of Pb–Zn Mineralization in the Pulang Cu Polymetallic Deposit in Yunnan Province, China: Insights from Analyses of Geology, Fluid Inclusions and C–H–O–S Isotopes

The Pulang super-large porphyry Cu polymetallic deposit, located in the Sanjiang area of Yunnan Province, is one of the largest Cu deposits in China. This deposit hosts Cu resources of ~5 × 106 t and other ore-forming elements, such as Mo, Au, Ag, Pb, Zn, Pt and Pd. Recently, obvious hydrothermal vein-type Pb–Zn mineralization, with a Pb + Zn resource of ~0.4 × 106 t, has been detected in the North Ore Section of the deposit. However, the genesis of these Pb–Zn ore bodies, especially their relationship to the major Cu ore bodies in the South Ore Section, remains controversial. We conducted geologic description, fluid inclusion petrography and microthermometry, and C, H, O and S isotope studies to uncover the genesis of Pb–Zn vein-type mineralization in North Pulang. As a result, three types of Pb–Zn veins were identified: a quartz–pyrrhotite–chalcopyrite–sphalerite–galena vein, a quartz–pyrrhotite–sphalerite–galena vein, and a calcite–quartz–pyrrhotite–galena vein. All fluid inclusions in the quartz from different veins are liquid-rich inclusions, with homogenization temperatures in the range of 184 °C–235 °C and salinities between 10.4 wt.% and 17.8 wt.% NaCl eq., indicating that the Pb–Zn ore-forming fluid was a single-phase fluid with a low temperature and low-to-medium salinity. Hydrothermal quartz in different stages displays δDwater values ranging from −46.9‰ to −120.0‰ (V-SMOW), and the calculated δ18Owater values range from 2.4‰ to 4.3‰ (V-SMOW), implying that the mineralization fluids likely originated from magma, with a minor involvement of meteoric water. The δ13CCal values (−2.3‰ to −7.9‰ V-PDB) of calcite indicate that C likely originated from a deep-seated source. The δ34S values of chalcopyrite, pyrite, pyrrhotite and sphalerite reveal that S was possibly derived from magmatic rocks. Based on the above data, it is suggested that the Pb–Zn mineralization in North Pulang was the result of the northward migration of ore-forming fluids that originated from South Pulang along the NE-trending structural fractures. A strong water–rock interaction occurred during the migration process. However, the involvement of meteoric water and accompanied cooling of fluids were most likely responsible for the precipitation of galena and sphalerite.

Magnetotelluric images of the medium enthalpy Bakreswar geothermal province within a granitic gneissic complex, Eastern Indian Peninsula

AbstractThe Bakreswar geothermal province represents a medium enthalpy geothermal system with its Bakreswar and Tantloie hot springs. It lies within the Chotanagpur Granite Gneissic Complex in the eastern part of the Indian Peninsula. The province has a high heat flow and a high geothermal gradient of 90°C/km. Magnetotelluric data from 95 sites in a frequency range of 10 kHz–10 Hz were acquired over the Bakreswar geothermal province to obtain an electrical conductivity model and map the geothermal reservoir with its fluid pathways and related geological structures. Subsurface conductivity models obtained from three‐dimensional inversions of the Magnetotelluric data exhibit several prominent anomalies, which are supplemented by gravity results. The conductivity model maps three features which act as a conduit (a) a northwest–southeast trending feature, (b) an east–west trending feature to the south of the northwest–southeast trending feature (which lies 1 km north of the Oil and Natural Gas Corporation fault marked by previous studies) and (c) shallow conducting features close to Bakreswar hot spring. The northwest–southeast trending feature coincides with the boundary of the high‐density intrusive block. This northwest–southeast trending feature provides the pathway for the meteoric water to reach a maximum depth of 2.7 km, where it gets heated by interacting with deep‐seated structures and then it rises towards the surface. The radiogenic process occurring within the granites of Chotanagpur Granite Gneissic Complex provides the heat responsible for heating the meteoric water. The northwest–southeast and east–west trending features are responsible for the transport of meteoric water to deeper depths and then towards the shallow regions of the Earth. The near surface features close to the Bakreswar hot spring are responsible for carrying the water further towards the hot spring. The resistivity of these structures plotted as a function of salinity and temperatures for saline crustal fluids suggests the involvement of meteoric water. Further, applying Archie's law to this resistivity suggests that the conduit path has a porosity greater than 10%. This study successfully maps the anomalous structures which might foster the migration of geothermal fluid in Bakreswar geothermal province.

Multiple mineralization events at Paleozoic Sanchakou porphyry Cu deposit, Xinjiang: New insights from geology, geochronology, fluid inclusions, and H-O-C isotopes

The Sanchakou Cu deposit is located in the eastern section of the Dananhu arc belt in Eastern Tianshan, Xinjiang, and recorded multiple magmatic-mineralization events. The porphyry-style mineralization period produced disseminated, sulfide-dominant veined, and patchy sulfides containing chalcopyrite ± bornite ± carrolite ± molybdenite (Mol-1), which was associated with magnetite ± biotite ± chlorite ± sericite alteration in a suite of quartz diorite intrusions. The overprinting mineralization period contributed to minor Cu and Mo mineralization, featured by later disseminated molybdenite (Mol-2), chalcopyrite, and widespread low-temperature (<280 °C) vein-type stellerite assemblages. Two distinct geological ages of molybdenite (including Mol-1 and Mol-2) from Sanchakou have been determined in this study. The old 187Re/187Os isochron age for euhedral Mol-1 represents the timing of original porphyry-style mineralization (386 ± 16 Ma), in agreement with LA-ICP-MS zircon U-Pb age of dark diorite dykes (390 ± 11 Ma). The young 187Re/187Os age for fine-grained Mol-2 is interpreted to be a maximum age of sulfide formation or remobilization (364 ± 15 Ma), most likely associated with the emplacement of Late Devonian gneissic granite intrusions. Fluid inclusion microthermometry, mineralogy, and physicochemical calculations for the porphyry-type mineralization period (including four stages) at Sanchakou suggest that earlier magmatic fluids have evolved from high T (310–460 °C), high logfO2 (−22 to − 26), and alkaline condition during stage I to low T, low logfO2 (−34), and acidic condition during stage II. The decrease of oxygen fugacity caused by abundant deposition of magnetite in stage I produced large-scale Cu and Mo precipitation. Stage II to IV fluids have gradually decreasing temperatures and salinities, due to involvement of meteoric water that also facilitates the ore deposition. This result is consistent with the evolution of O isotope compositions of the fluids (δ18Ofluids = − 9.3 to 4.3), further implying the significance of fluid mixing instead of fluid boiling that caused ore deposition. Locally high-grade copper concentrations at Sanchakou are likely attributed to the overprinting modification event on the original ore bodies. All of these observations indicate that the Paleozoic Sanchakou ore-forming system is similar to other deformed porphyry Cu systems in the Central Asian orogenic belt (CAOB) and worldwide. The Cu mineralization and modification event at Sanchakou is coincident with the second peak productivity in CAOB. We further suggest that the Paleozoic diorite complex and stellerite alteration can be as a significant exploration target for porphyry-style Cu mineralization in the Eastern Tianshan.

Origin of breccia dolomites in the middle Devonian Guanwushan Formation, NW Sichuan Basin, China: Implications for ultra-deep carbonate reservoirs

Deep to ultra-deep carbonate rocks have become a target for hydrocarbon exploration. The formation mechanisms of these deep to ultra-deep reservoirs are very complicated, and no consensus has yet emerged. This paper reports an investigation into the Middle Devonian Guanwushan Formation in the NW Sichuan Basin, China, which is a typical ultra-deep dolomite reservoir. Drilling-core and thin-section observations identified breccia matrix dolomite (MD) and interbreccia-filling dolomite (FD), of which the FD is commonly associated with sphalerite and barite. Geochemical analyses, including C and O isotopes, trace and rare earth element (REE) contents, and fluid inclusions, were conducted to investigate the origins of the different types of dolomite. Results indicate that the MDs generally retain the signature of syn-depositional seawater (relatively positive δ18O, low Fe and Mn, left-leaning REE patterns, and negative Ce anomalies), with involvement of meteoric water (relatively high Al, Ti and ΣREE). In contrast, the FDs were the diagenetic product of deep hydrothermal fluids (depleted δ18O, high Fe and Mn, and enrichment in MREEs), and the homogenization temperature of fluid inclusions is much higher than the normal burial geothermal temperature. The breccia dolomite reservoirs of the Guanwushan Formation were deposited as reef-core micro-facies and formed during the depositional to early diagenetic stages, and were the result of subaerial seawater dolomitization and meteoric water karstification. However, hydrothermal fluids subsequently modified the reservoir by cementation and filling. The Guanwushan Formation is a typical case of an ultra-deep carbonate reservoir that formed during the depositional to early diagenetic stages but was filled at the burial stage. Therefore, the favorable reservoir zones associated with deposition and early diagenesis should be the targets of future exploration. The findings of this study are expected to be of general significance for deep and ultra-deep oil and gas exploration in other regions and countries.

When rainfall trapped in fluid inclusion restores the relief of an orogen: Insights from the Cenozoic Himalayas

The involvement of meteoric water in orogens dynamics through surface processes is well known as for example in the Himalayas where erosion, resulting of the interplay between climate and tectonics shapes the most spectacular landscapes on the planet. But what about more internal and deepest surface fluid infiltration? Here we report analysis of the δ18O(water) and δD(water) of extracted water from fluid inclusions hosted into Cenozoic quartz veins sampled in the core of the Himalayan range, near the Main Central Thrust and the South Tibetan Detachment. Isotopic and microthermometric values suggest a meteoric origin for the fluids trapped in the quartz of syn- to post-kinematic veins formed between 10 to 20 km depth. Moreover, the isotopic compositions obtained in this study on quartz fluid inclusions water collected along a transect across the Himalayan range evolved with the topography in a similar manner than the modern meteoric water. Considering the age of formation of the quartz veins between 18 and 12 Ma, we deduce that the morphology of the Himalayan topographic front was already shaped during the Miocene but located further north.

Source of gold and ore-forming processes in the Zarshuran gold deposit, NW Iran: Insights from in situ elemental and sulfur isotopic compositions of pyrite, fluid inclusions, and O−H isotopes

The Zarshuran gold deposit (155 t Au, average grade: 2.63 g/t), NW Iran, provides a new paradigm for understanding the multicomponent ore-forming processes and metallogeny of gold during the evolution of hydrothermal fluids. It is characterized by auriferous quartz veins and gold coexisting with disseminated Fe-As-S sulfide minerals that are hosted in a sequence of Early Cambrian metasedimentary rocks. A complex paragenesis is defined by five sulfide stages: pre-ore stage pyrite (Py0), early ore-stage pyrite (Py1 and Py2), middle ore-stage pyrite (Py3a, Py3b, and Py3c), late ore-stage pyrite (Py4), and post ore-stage pyrite (Py5). Py0 with framboidal texture is characterized by relatively low concentrations of As, Au, Cu, and Sb, and has a broad range of negative δ34S values from −28.2 to −3.7 ‰, indicating microbial reduction of marine sulfate. Py1 and Py2 show porous texture with As-rich bright bands also having high Au (mean: 18.4 ppm). Similarly, narrow ranges in δ34S from −3.6 to +3.2 ‰ likely suggest a deep-seated magmatic sulfur source. In the middle ore-stage, Py3a cryptocrystalline cores have a range of positive δ34S (+5.4 to +26.7 ‰) values and high concentration of As(-Au), whereas later well-crystallized outer rim Py3c is Co(-Ni) rich, has a much more restricted δ34S range (−2.9 to +1.4 ‰), indicating an evolution of fluid composition from As-rich to Co-rich. Most of the gold (mean: 20.2 ppm) and trace elements (Hg, Ag, Sb, and Tl) were deposited in Py4, whose δ34S values (+5.4 to +26.7 ‰) show that ore fluid sulfur in this stage was mainly sourced from a mixture of magmatic sulfur with minor input of reduced sedimentary rocks. Low gold and trace element content with slightly negative δ34S values (–8.5 to –4.2 ‰) of Py5 show that they were likely formed from a metal-poor oxidizing fluid.The mineralizing fluid system can be described as carbonic-aqueous with low to moderate salinity (3.2–15.1 wt% NaCl equiv.) and medium temperature of 285 to 317 °C (early ore-stage) and 255 to 290 °C (late ore-stage), which suggests that phase separation was responsible for gold precipitation during late ore-stage As-Hg-Sb sulfide veins. The δ18Ofluid ranges from −7.8 to +4.2 ‰, and the δD values for fluid inclusions in mineral range from −105 to −65 ‰, suggesting involvement of meteoric water during late- to post ore-stages. Our results indicate that the Zarshuran is a distal disseminated gold deposit formed during southward subduction of the Proto-Tethys oceanic lithosphere beneath the northern margin of Gondwanan terranes through the early Cambrian.

Zircon texture and composition fingerprint HREE enrichment in muscovite granite bedrock of the Dabu ion-adsorption REE deposit, South China

More than 90% of the global heavy rare earth elements (HREE) supply is currently from the ion-adsorption REE deposits in South China. However, the mechanism of HREE enrichment in granite bedrock of REE mineralized weathering crusts remains poorly understood. In this study, we present a comprehensive investigation on zircon texture and composition as a proxy to unravel the magmatic-hydrothermal processes which resulted in HREE enrichment of the Dabu muscovite granites. Our results show that zircon in the Dabu muscovite granites can be classified into three types based on morphology, internal structure and chemical compositions. The early-magmatic zircon grains (ZrnI) are prismatic crystals with bright oscillatory zoning, and crystallized early in the granitic magma. The late-magmatic zircon grains (Zrn-II) occur as murky euhedral or subhedral crystals or as overgrowth on ZrnI, and crystallized from a volatile-enriched residual melt in the late magmatic stage. The hydrothermal zircon (Zrn-III) is anhedral without oscillatory zoning, possibly formed via intense hydrothermal alteration of Zrn-II in the hydrothermal stage. Raman spectra show a decrease in degree of crystallinity from Zrn-I to Zrn-III. In-situ compositional and isotopic analyses suggest that zircon geochemistry is a good proxy for the magmatic-hydrothermal processes of the host granite. Zircon UPb dating yields similar ages of 155.3 ± 1.4 Ma (2σ) and 154.1 ± 1.0 Ma (2σ) for Zrn-I and Zrn-II, respectively. The decrease of Zr/Hf from Zrn-I to Zrn-III indicates that the Dabu muscovite granites underwent magmatic to hydrothermal evolution. Furthermore, the decreasing δ18O values of Zrn-I to Zrn-III suggest the increasing involvement of meteoric water in the fluids. Significantly, compared with Zrn-I and Zrn-II, Zrn-III has the highest U, Hf and REE, in particular HREE. The LREE/HREE ratios decrease with the increase of REE contents and the decrease of Zr/Hf ratios from early to late zircon of the granite bedrock of ion-adsorption HREE deposits, which is significantly different from those of carbonatite-alkaline related REE deposits. The significant increase of HREE concentrations in early to late zircon should be ascribed to the introduction of HREE-rich fluids during magma evolution. Therefore, we propose that the HREE-rich fluids from magma exsolution metasomatized the granites to achieve further enrichment of HREE, which is an important prerequisite for the formation of ion-adsorption HREE deposits. Accordingly, we argue that zircon composition can be used as a chemical indicator for the REE behaviors in magmatic-hydrothermal systems that are vital to the formation of REE deposits.

The Baogutu gold deposit in west Junggar, NW China: An epizonal intrusion-related gold deposit

The Baogutu gold deposit (∼4 Mt ore @ 5.5 g/t Au) in West Junggar, is hosted by Early Carboniferous volcano-sedimentary rocks and Late Carboniferous dioritic dikes. Both the dikes and gold mineralization are controlled by NE-trending faults. Two diorite dikes in direct spatial association with gold-bearing quartz veins have LA–ICP–MS zircon U–Pb ages of 316 ± 5 Ma and 314 ± 3 Ma, respectively. The emplacement ages of the dikes are a little older than reported gold mineralization ages (312–311 Ma), which is consistent with their crosscutting relationships. Gold mineralization occurs in quartz veins and stockworks in altered tuff, tuffaceous siltstone, silty mudstone, and dikes. Three gold-bearing vein stages have been identified: (I) pyrite–quartz veins in the deep part of the system; (II) stibnite–quartz veins and (III) native arsenic–quartz veins at shallower-level. Fluid inclusion study shows that the pyrite–quartz veins of stage I formed at temperatures between 345 and 265 °C from fluids with salinities of 5.1–9.1 wt% NaCl equiv, whereas the native arsenic–quartz veins of stage III formed at ∼200 °C from fluids with salinities of 1.4–3.9 wt% NaCl equiv. The ore-forming pressure is estimated to be ∼50–62 MPa, corresponding to mineralization depth of ∼3.3–4.0 km. Oxygen and hydrogen isotope compositions of the fluids (δ18OH2O = 7.9 to 11.2 ‰, δD = -88 to −96 ‰) indicate that the initial hydrothermal fluids have a magmatic source, with involvement of meteoric water in the late stage. The in-situ lead isotopic compositions of pyrite in stage I pyrite–quartz veins are similar to those of bulk sulfide minerals in the Baogutu porphyry Cu deposit, and close to the porphyry stocks, whereas the stibnite and native arsenic in stage II and III quartz veins have more radiogenic lead isotopic signatures due to water–rock exchange with the wall rocks. The Baogutu gold deposit shows affinities to epizonal gold deposits in intrusion-related gold systems (IRGS). The IRGS model suggests that, sheeted, disseminated and vein-type Au–As–Bi mineralization might be found hosted in dioritic to granitic stocks and proximal strata, and vein-type Au–As–Sb mineralization in distal faults.

Ore-forming fluid evolution of a porphyry Cu-Mo deposit coexisting with porphyry Mo systems in a post-collisional setting, Xiaokelehe, NE China

The Xiaokelehe porphyry Cu-Mo deposit in the Great Xing’an Range contains six stages of quartz-sulfide veins (V1 to V6) including potassic (V1 to V4), chlorite-illite (V5) and phyllic (V6). Two to three types of quartz were identified within each stage, of which the V2Q1, V3Q1, V4Q2, V5Q1 and V6Q2 are spatially associated with sulfides. Three types of fluid inclusions were identified in these veins, i.e., type I aqueous inclusions homogenized to liquid, type II aqueous inclusions homogenized to vapor, and type III aqueous inclusions containing halite and homogenized to liquid. Type I and type II primary inclusions occur in all stages, and type III inclusions are developed in V2 to V4 veins. Microthermometric data show that the maximum formation temperatures and pressures of V2-V6 veins of type I inclusions are 353 to 437 °C and 19.0 to 27.6 MPa, 309 to 415 °C and 15.0 to 30.1 MPa, 330 to 365 °C and 16.7 to 27.6 MPa, 243 to 351 °C and 13.9 to 18.9 MPa and 255 to 347 °C and 13.9 to 17.8 MPa, respectively, which show a decreasing trend. Oxygen isotope data show that the δ18OH2O values of V2-V4 veins (5.3 to 10.4 ‰) are consistent with typical magmatic values, whilst the δ18OH2O values of V5-V6 veins (0.2 to 4.6 ‰) are much lower than those of the magmatic water, which is due to involvement of meteoric water. The fluid inclusion microthermometry and O isotope data suggest an evolving magmatic-hydrothermal system with decreasing temperatures, pressures from V2 to V4 veins (potassic stage) to V5 (chlorite-illite stage) and V6 veins (phyllic stage), and an increasing incorporation of meteoric water in V5 and V6. The Xiaokelehe deposit has lower CO2 contents than the adjacent porphyry Mo deposits formed in the same post-collisional setting, which is mainly due to differences of mineralization depths and magma source. The formation of porphyry deposits with different Mo/Cu ratios highlights the diversity and complexity of the mineralizing systems in post-collisional settings, which has important implications for mineral exploration in such environments.

Fluid evolution characteristics and ore genesis in the Jinqu Au deposit, Qinling Orogen, China: Implications for ore genesis

The Jinqu Au deposit is located in the central Xiaoqinling gold field along the southern margin of the North China Craton. Ore-bearing auriferous quartz veins in the deposit are controlled by E–W trending structures within amphibolite facies metamorphic rocks of the Archean Taihua Group. The ore-forming process in this deposit can be divided into four stages represented by feldspar-quartz, pyrite-quartz, polymetallic sulfide-quartz, and carbonate-quartz veins and veinlets. Here we present fluid inclusion and isotopic data of the Jinqu Au deposit. Four types of fluid inclusions in quartz and calcite are identified, including carbonic-aqueousinclusions (type-1), aqueousinclusions (type-2), solid-bearinginclusions (type-3) and pure carbonic inclusions (type-4) varieties, based on petrography and laser Raman spectroscopy. Quartz in stage I contains type-1 fluid inclusions (FIs) which homogenized to aqueous or carbonic phase at temperature 361 to 406 ℃ and 385 to 400 ℃ respectively, and have salinities of 10.3 to 17.9 wt% NaCl equiv. Type-2 FIs show homogenization temperatures of 347 to 410 ℃ into the liquid phase, with high salinities of 11.6 to 18.6 wt% NaCl equiv. Quartz in stage II is the major host of type-1 FIs, with minor type-4 FIs, the former showing homogenization at temperatures of 305 to 390 ℃ into the carbonic phase and 280 to 410 ℃ into the aqueous phase, with variable salinities of 4.5 to 19.8 wt% NaCl equiv. The stage III quartz contains all the four types of FIs (homogenizing to carbonic or aqueous phase at temperature 309 to 360 ℃ and 295 to 400 ℃, with salinities of 6.6 to 19.9 wt% NaCl equiv for type-1, and homogenizing to liquid at temperature 308 to 326 ℃ with salinities of 12.5 to 13.2 wt% for type-2 Fls). In stage IV, type-2 FIs are the major type in quartz and calcite with total homogenization temperatures of 213 to 280 ℃ into the liquid phase and variable salinities of 5.3 to 18.6 wt% NaCl equiv. Our data show that the ore-forming fluids of the Jinqu Au deposit are generally characterized by moderate to high homogenization temperatures and variable salinities, belonging to the CO2-H2O-NaCl ± CH4 system. Based on fluid inclusion data, we infer that fluid immiscibility occurred in stages II and III, and the estimated trapping pressures for stages II and III fluids are between 81 and 275 MPa.The CHO isotopic values of fluids (δ18Owater = 1.2 to 6.4 ‰; δDV-SMOW = − 68.5 to − 56.0 ‰; δ13CCO2 = − 12.4 to − 3.4 ‰) in stage I to IV and δ13CV-PDB values for calcite (δ13CV-PDB = − 7.6 to − 4.3 ‰) in stage IV suggest that the ore-forming fluids were composed of a mixture of metamorphic water and mantle-derived fluids with minor involvement of meteoric water. Fluid inclusions in pyrite of stage II and III yield 3He/4He ratios of 0.88 to 1.39 Ra, and considerable 40Ar/36Ar ratios range from 2287.6 to 5669.9, suggesting the mixing of mantle and crustal components. The δ34SV-CDT values of sulfide samples in stages II and III range from − 5.8 to 4.5 ‰ (except for a pyrite grain within calcite that shows − 28.5 ‰). The values of 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb of pyrite samples in stages II and III are from 16.919 to 17.321, 15.340 to 15.539, and 37.303 to 37.971 respectively. Our data suggest that the Taihua Group was possibly a major source for the ore-forming metals of the Jinqu Au deposit. Integrating the data from ore geology, fluid inclusions, isotope geochemistry and regional setting, we propose that the Jinqu Au deposit is an orogenic-type deposit which formed within the continental collision setting of the North China and Yangtze Cratons.

Titanite geochemistry and textures: Implications for magmatic and post-magmatic processes in the Notch Peak and Little Cottonwood granitic intrusions, Utah

Abstract Textural and compositional variations in titanite constrain the roles of magma mixing and hydrothermal alteration in two plutons in central Utah: the Jurassic Notch Peak and the Oligocene Little Cottonwood stocks. In the Notch Peak intrusion, magmatic titanite grains usually have oscillatory zones combined with BSE-bright sector zones, in some cases surrounding simple unzoned cores. These grains are frequently overprinted by hydrothermal titanite with low concentrations of high field strength elements (HFSE). Magmatic titanite has an average δ18O of 6.0‰ and post-magmatic titanite is 6.2‰, as analyzed by SIMS. Average Zr-in-titanite temperatures are also similar, with 718 °C for magmatic and 711 °C for hydrothermal titanite. These observations indicate simple magmatic growth, followed by hydrothermal alteration by magmatic fluids. Titanite in aplite dikes and sills has lower concentrations of all trace elements except F. Many titanite grains in the aplites have late overgrowths of high-Fe titanite. This high-Fe titanite has δ18O of 6‰ and an average Zr-in-titanite temperature of 718 °C and likely precipitated from a last flush of exsolved magmatic water enriched in Cl and Fe. Titanite in the Little Cottonwood stock typically has distinct patchy cores with rounded and embayed ilmenite inclusions. Mafic enclaves have abundant titanite that is similar in texture and δ18O (5.1‰) to titanite in the host (δ18O = 4.9‰), but it has a slightly higher average Zr-in-titanite temperature (731 vs. 717 °C). The patchy cores in the enclaves have the highest average Zr-in-titanite temperature (759 °C) and distinctive REE patterns. The textural and compositional data indicate that a hotter, more reduced, ilmenite-bearing mafic magma mixed into an oxidized felsic magma, destabilizing existing ilmenite and allowing crystallization of titanite. In the granodiorite and in the enclaves, hydrothermal growth of titanite is evidenced by distinct narrow rims as well as anhedral titanite that grew between sheets of chloritized biotite. Secondary hydrothermal titanite typically has lower concentrations of most HFSE, but is relatively enriched in F, Mg, Mo, and U, and it has higher Nb/Ta and lower Th/U ratios. Post-magmatic titanite also has strikingly different REE patterns than magmatic titanite, including the absence of pronounced Eu anomalies and lower REE abundances. These chemical features are controlled by element solubilities in aqueous fluids. In most cases, hydrothermal titanite has δ18O values similar to magmatic titanite, indicating alteration and recrystallization from exsolved magmatic fluids. The involvement of meteoric water with low δ18O is evident locally; individual spots have δ18O as low as 1.7‰ in the Little Cottonwood stock. Titanite compositions and textures provide important insights into the origins of granitic rocks and can be used to distinguish separate batches of magma, gauge the evolution of magmatic rocks, assess mixing processes, and infer compositions of mixing components. Because titanite also forms hydrothermally, it retains hints about the composition, temperature, and oxygen fugacity of the hydrothermal fluids and reveals details about titanite-forming reactions. However, the Al-in-titanite geobarometer does not yield realistic pressures of crystallization and the use of titanite as a geochronometer is compromised by the development of U-rich hydrothermal titanite.

Garnet and scheelite chemistry of the Weijia tungsten deposit, South China: Implications for fluid evolution and W skarn mineralization in F-rich ore system

Fluid evolution is an essential subject in the studies of hydrothermal ore-forming processes. Garnet and scheelite prevail in W-bearing skarn deposits and record plentiful information on W skarn mineralization. In-situ LA-ICP-MS trace element analyses have been carried out on the garnet and scheelite from the F-rich Weijia W deposit in South China to constrain the processes of fluid evolution and W skarn mineralization. The Weijia W deposit mainly consists of calcic and magnesian skarns and was formed through six stages of alteration and mineralization. Two stages of fluid exsolution are recognized in the magmatic-hydrothermal system. The earlier exsolved fluids are Cl-rich with rightward-sloping REE patterns and result in pre-ore skarnization. The later exsolved fluids are F-rich with relatively flat REE patterns and are responsible for W mineralization. The pre-ore garnets are LREE-enriched and HREE-depleted whereas the syn-ore garnets are LREE-depleted and HREE-enriched with lower δEu values than the former, denoting a transition from wall rock-controlled to magmatic fluid-dominated fluid-rock interaction. Combined with the skarn occurrences, mineral assemblages, and garnet textures, it is revealed that the mechanism of skarn formation shifts from more diffusive metasomatism under lower water/rock ratios to more advective metasomatism at higher water/rock ratios. The advective metasomatism with a high flux of ore-forming fluids is hydrodynamically favorable for the consequent W mineralization. The earliest-formed scheelite is akin to the host granite porphyry in REE patterns and can reflect the features of initial mineralizing fluids. It has high ΣREE (1255–5059 ppm), Y (616–1416 ppm), Nb (585–2629 ppm), Ta (14–248 ppm), Mn (up to 1977 ppm) and low Mo (mostly < 1000 ppm) contents, indicating that the primary F-rich magmatic fluids are reduced and enriched in REEs, Y, Nb, and Ta. The contents of ΣREE, Y, Nb, and Ta in scheelite are decreasing with the evolution of the F-rich mineralizing fluids. The latest-formed scheelites have distinctly lower ΣREE (2.9–140 ppm), Y (0.01–4.1 ppm), Nb (1.7–77 ppm), and Ta (0.04–0.19 ppm) contents and higher (La/Yb)N ratios and δEu values. They show 1:1 positive correlation of EuN vs. EuN* and have high Mo (up to 129466 ppm) and low Mn (as low as 3.4 ppm) contents, implying involvement of meteoric waters in the evolved ore-forming fluids and an oxidizing condition. Fluid-rock interaction, mineral precipitation, and fluid mixing largely control the process of fluid evolution. Fluorine consumption due to the formation of fluorite and the other F-rich minerals is vital for the compositional evolution of F-rich mineralizing fluids. The decrease of F concentration in fluids will depress the solubilities of REEs, Y, Nb, and Ta and enhance the LREE/HREE fractionation. Greisenization and skarnization induced the neutralization of the acidic W-bearing fluids and the liberation of Ca from the granite porphyry and carbonate strata and then triggered the scheelite precipitation. The carbonate strata contain abundant Ca and the granite porphyry is poor in Ca, and thus the economic W mineralization dominantly occurs in the skarns.

Origin of the dioritic porphyrite and its associated Matouniu skarn gold polymetallic deposits in the Eastern Hebei Province, North China: Evidence from geochronology, geochemistry, and C–O–S–Pb–Hf isotopes

The Matouniu gold polymetallic deposit in the Eastern Hebei Province (Jidong) in the northern margin of the North China Craton (NCC) is a skarn‐type ore deposit. Geochemical data, zircon U–Pb, and Hf isotope analysis of the mineralization‐related dioritic porphyrite and C–O–S–Pb isotopes from the deposit were used to investigate the origin, magmatic evolution, mineralization, and tectonic setting of the Matouniu gold polymetallic deposit. Zircon U–Pb dating reveals an emplacement age of 146.7 ± 1.1 Ma, indicating that the magmatism and mineralization occurred during the Late Jurassic. Geochemical, Hf, and Pb isotopic compositions indicate that the dioritic porphyrite was formed by the partial melting of the ancient mafic lower crust, leaving behind residual plagioclase, amphibole, and garnet, with traces of mantle material involvement. The S and Pb isotopic compositions revealed that both the ore‐forming materials and the dioritic porphyrite were derived from a deep‐seated magmatic source, which mainly originated from the lower crust, with minor input from the mantle. The C–O isotopic compositions suggest that the early ore‐forming fluids had a mainly deep‐seated magmatic source with minor meteoric water involvement, and were accompanied by continuous meteoric water involvement and water‐rock interaction during the fluid migration. The Matouniu gold polymetallic deposit and Late Jurassic dioritic porphyrite associated with skarn mineralization formed under geodynamics involved a compressional regime that was associated with the continuous subduction of the Palaeo‐Pacific Plate beneath the East Asia Plate.

Fluid inclusions, isotopes and mineralogy of the Kuruer epithermal Cu-Au deposit, Chinese Western Tianshan: Implications for ore genesis and exploration

The Kuruer Cu-Au deposit is located in the Wusun Range of Yili Block, Chinese Western Tianshan, where numerous epithermal Au, skarn Fe-Cu and porphyry Mo-Cu deposits have been recognized. Petrography, fluid inclusions, S-Pb-H-O isotopes, field emission-scanning electron microscopy (FE-SEM) plus energy dispersive spectrometer (EDS) and electron microprobe analysis (EMPA) have been carried out to constrain the genesis of the Kuruer deposit and its implication for further exploration. The minerlization is hosted by volcanic rocks and occur as veins and veinlets structurally controlled by NW-trending faults. Three ore-forming stages were recognized, including quartz-sulfides-bismuth-gold stage (I), quartz-chalcopyrite stage (II) and calcite-chlorite-chalcopyrite stage (III).Six types of fluid inclusions were identified in stage I quartz, including monophase vapor inclusions (type 1), liquid-rich biphase inclusions (type 2), vapor-rich biphase inclusions (type 3), H2O-rich CO2-H2O triphase inclusions (type 4), CO2-rich CO2-H2O triphase inclusions (type 5) and solid halite-bearing triphase inclusions (type 6), whereas only type 2 inclusions were recognized in stage II quartz and stage III calcite. Types 2, 3, 4 and 6 inclusions in stage I have homogenization temperature (Th) ranges of 184–359 °C, 209–252 °C, 250–319 °C and 229–263 °C, with salinity ranges of 4.1–8.5 wt% NaCleq, 5.9–6.9 wt% NaCleq, 1.0–6.0 wt% NaCleq and 32.7–33.9 wt% NaCleq, respectively. Type 2 inclusions in stages II and III have Th varying from 144 to 212 °C and 114 to 163 °C, with salinities of 0.2–6.7 wt% NaCleq and 0.1–3.1 wt% NaCleq, respectively.The in-situ δ34S values of sulfides in stage I range from −4.66 to 0.34‰. The 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb ratios of stage I chalcopyrite vary from 18.295 to 18.954, 15.568 to 15.673 and 38.109 to 38.817, respectively, which are consistent with those of Early Carboniferous Dahalajunshan Formation volcanic rocks and granitoids from the Wusun Range. The values of δ18OH2O-VSMOW calculated from δ18Oquartz and δDH2O-VSMOW of stage I quartz range from 0.0 to 2.4‰ and −118.6 to −109.3‰, respectively. These isotopic compositions indicate that both metals and sulfur were sourced from the hosting volcanic rocks and hidden causative pluton, while the initial ore-forming fluids were magmatic in origin, with increasing involvement of meteoric water with time.Evidence from mineralogy, mineral geochemistry and fluid inclusions indicates that the initial fluid phase separation triggered the precipitation of “invisible” gold within pyrite and chalcopyrite during stage I. Subsequently, the decrease of fS2 due to the escape of H2S(g) and sulfide precipitation and cooling caused the formation of liquid bismuth from solutions. The bismuth melts have scavenged Au in situ from the residual solutions, resulting in the formation of Bi-Au inclusions within the fractures and intergranular spaces of earlier pyrite. For stages II and III, dilution and cooling due to input of meteoric water facilitated the chalcopyrite precipitation. The Kuruer Cu-Au deposit is classified as a subepithermal mineralization associated with porphyries. Porphyry Cu-Au mineralization could have developed beneath the Kuruer and its vicinity.

Genesis and fluid evolution of the Yuku porphyry Mo deposit, East Qinling orogen, China

The Yuku is a large porphyry Mo deposit (1.5 Mt at 0.12% Mo) in the Luanchuan ore district of the East Qinling orogen, central China. The economic Mo ore bodies occur as veins, veinlets, and disseminated ore and are developed mainly within the late Mesozoic Yuku porphyritic granite. Molybdenum mineralization is generally associated with potassic and phyllic alteration. Hydrothermal processes in the Yuku deposit are divided into four stages: (I) a quartz–K‐feldspar–biotite ± pyrite stage, (II) a quartz–molybdenite ± pyrite ± K‐feldspar ± sericite stage, (III) a quartz–polymetallic sulphide stage, and (IV) a calcite ± quartz ± fluorite ± pyrite stage. The fluid evolution during these hydrothermal stages was constrained through systematic investigation of fluid inclusions (FIs) and H−O isotopes. Four types of primary or pseudosecondary FIs were recognized in hydrothermal quartz and calcite: two‐phase liquid‐rich inclusions (L‐type), two‐phase vapour‐rich inclusions (V‐type), halite‐bearing (hypersaline) inclusions (H‐type), and three‐phase CO2‐bearing inclusions (C‐type). FIs within Stages I–IV have homogenization temperatures of 375 to &gt;550, 297–400, 198–298, and 149–188°C, with salinities of 0.53–13.18, 0.35–40.23, 5.11–11.81, and 5.71–9.73 wt% NaCl equiv., respectively. In Stage I, coexisting vapour‐rich (V‐type) and liquid‐rich (L‐type) FIs have similar homogenization temperatures (488 to &gt;550°C) and distinct salinities, indicating fluid boiling during the formation of quartz–K‐feldspar–biotite veins at a pressure of 550–700 bar and a lithostatic depth of 2.3–2.8 km. In Stage II, FIs in quartz were also trapped under boiling conditions, as evidenced by coexisting hypersaline H‐type (34.13–40.23 wt% NaCl equiv.) and low‐salinity V‐type (0.35–2.24 wt% NaCl equiv.) inclusions, which formed at temperatures of 309–361°C and hydrostatic depths of 1.0–2.0 km, equivalent to pressures of 100–200 bar. During Stage III, the ore‐forming fluids were cooler (198–298°C) and more dilute (5.11–11.81 wt% NaCl equiv.) due to the involvement of meteoric water, with minimum trapping pressures estimated at &lt;100–150 bar, corresponding to a hydrostatic depth of &lt;1.0 km. In Stage IV, temperatures decreased further to 149–188°C, with lower salinities (5.71–9.73 wt% NaCl equiv.), indicating a post‐ore fluid stage. These data suggest that the mineralizing fluids forming the Yuku Mo deposit changed from early moderate‐ to low‐salinity CO2‐rich fluids in the H2O–NaCl–CO2 system that formed at high temperature and pressure, to late H2O–NaCl low‐salinity fluids that formed at low temperature and pressure. H−O isotopic compositions indicate that the mineralizing fluids had a dominantly magmatic signature but were diluted by meteoric waters. Combining our integrated analysis of the fluid evolution and deposit geology, we propose that fluid boiling and fluid–rock interaction, including intensive potassic alteration, changed the salinity and triggered CO2 escape, leading to a decrease in fO2 and an increase in the acidity of the ore‐forming fluids, which ultimately controlled the deposition of molybdenite in the Yuku Mo deposit.

Genesis of HarizhaAg–Pb–Zndeposit in the eastern Kunlun Orogen,NWChina: Evidence of fluid inclusions andC–H–O–S–Pbisotopes

AbstractThe Harizha Ag–Pb–Zn deposit is located in the eastern part of the eastern Kunlun Orogen, NW China. Two episodes including five paragenetic stages of vein mineralization has been recognized for the Harizha Ag–Pb–Zn deposit through petrographic observation: quartz + pyrite + arsenopyrite (Stage I), quartz + pyrite + chalcopyrite + pyrrhotite (Stage II), quartz + pyrite + chalcocite + pyrrhotite + sphalerite + galena + pyrargyrite (Stage III), quartz + calcite + pyrite + tetrahedrite + pyrolusite (Stage IV), and calcite + covellite + malachite + goethite + graphite (Stage V). In the quartz or calcite three types of fluid inclusions (FIs) were identified: L‐type, C‐type, and S‐type. The S‐type inclusions are only found in quartz in the wall rocks. The C‐type inclusions occur in quartz from early episodes (Stage I and II). The FIs from the early episodes homogenized at 240–320°C, with salinities of 9–12 wt.% NaCl equivalent. The ore‐forming fluids at the early episodes belong to an H2O–CO2–CH4–NaCl system. The FIs from late episodes (Stage III and IV) homogenized at 140–240°C, with salinities of 2–8 wt% NaCl equivalent. The ore‐forming fluids from the late episodes are dominated by an H2O–NaCl fluid system. The HO and CO isotopic compositions of quartz and calcite indicate that the ore‐forming fluids were derived from a primary magmatic‐hydrothermal system, with subsequent meteoric water involvement at a later stage. Sulfides have δ34S values of −3.7 to –1.0‰, and206Pb/204Pb,207Pb/204Pb, and208Pb/204Pb ratios ranging from 18.381 to 18.425, 15.661 to 15.683, and 38.498 to 38.677, respectively. These likely suggest a magmatic sulfur affinity combined with the ore features, mineral associations, alteration characteristics, ore‐forming environment, and fluid evolutionary process. We conclude that the Harizha Ag–Pb–Zn deposit is a typical medium‐low temperature hydrothermal deposit.

Genesis of the Nailenggele Mo-Cu-Pb-Zn polymetallic orefield in the Boluokenu Metallogenic Belt, Western Tianshan, China: Constraints from geochronology, fluid inclusions and isotope geochemistry

The Nailenggele orefield, located in the northwestern Chinese Tianshan Orogenic Belt, is composed of the Lailisigao’er Mo deposit, No. 3571 Cu prospect and Qixing Pb-Zn deposit. Lailisigao’er is a typical porphyry deposit with characteristic veinlet-disseminated ores and potassic, phyllic and propylitic alterations. No. 3571, situated in the peripheral of Lailisigao’er, is characterized by large amounts of oxidized ores at surface with limited intrusions outcropped. Qixing, about 3 km from Lailisigao’er, is characterized by quartz-sulfide veins controlled by fractures. This study aims to examine the genetic relationships between these deposits and/or occurrences, and discuss the significance for further exploration in the orefield and elsewhere in the region. LA-ICP-MS U-Pb dating on zircons from the ore-bearing porphyry in the Lailisigao’er deposit yielded an age of 367.5 ± 4.8 Ma. The molybdenite Re-Os and sphalerite Rb-Sr isochron ages recalculated from previously published data are 365.9 ± 2.1 Ma for Lailisigao’er and 362.0 ± 5.7 Ma for Qixing, respectively, suggesting that they are coeval and both related to the granodiorite porphyries. Three types of fluid inclusions occur in the Mo-bearing quartz from Lailisigao’er, including two-phase aqueous inclusions (Type I), solid mineral-bearing aqueous inclusions (Type II) and CO2-H2O inclusions (Type III). The total homogenization (Th) temperatures cluster from 260 to 320 °C (to liquid) for type I inclusions, 310 to 332 °C (to liquid) for type II inclusions, and 268 to 324 °C (to CO2 phase) for type III inclusions. The salinities are mainly in the ranges of 2.0–8.0, 32.9–42.0, and 1.4–5.5 wt% NaCleq for types I, II and III inclusions, respectively. By contrast, only type I inclusions were identified in the Pb-Zn-bearing quartz from Qixing, with Th values of 149–261 °C and salinities of 1.7–5.3 wt% NaCleq. The δ34SCDT values of hydrothermal sulfides from Lailisigao’er, No. 3571 and Qixing range from 2.8‰ to 4.0‰, 4.0‰ to 4.6‰ and 0.7‰ to 4.9‰, respectively. Sulfides from these three locations have uniform Pb isotopic compositions. The (87Sr/86Sr)0 ratios of fluid inclusions (average 0.70971) in Mo-bearing quartz at Lailisigao’er and sphalerite (average 0.71020) at Qixing are similar to those of Mo-mineralized porphyries (average of 0.70886) from Lailisigao’er. The δ18OH2O and δDH2O values of Pb-Zn-bearing quartz from Qixing are similar to those of Mo-bearing quartz from Lailisigao’er, both plotting close to the field of magmatic water but shifted toward the meteoric line. These geochronological, fluid inclusions and isotopic data suggest that the mineralization at different localities in the Nailenggele orefield constitutes part of an integrated magmatic-hydrothermal system centered on the Lailisigao’er porphyry Mo deposit, with the Qixing Pb-Zn polymetallic deposit representing a distal end-member. Both metals and sulfur were dominantly derived from porphyritic intrusions, whereas the ore-forming fluids were initially derived from the magmatic intrusions, with increasing involvement of meteoric water in time and distance from magmatic-hydrothermal center. Fluid immiscibility in the early stage and fluid mixing in the later stage, together with cooling, were responsible for ore precipitation. Based on this mineralization model, it is inferred that concealed porphyry Cu-Mo mineralization may be developed underneath the No. 3571 and Qixing.

Genesis of the Hardat Tolgoi Ag-Pb-Zn deposit, Inner Mongolia, northeast China: Constraints from geology, fluid inclusions, and C-O-S-Pb isotope systematics

The Hardat Tolgoi Ag-Pb-Zn deposit (4.3 Mt at 3.15% Pb + Zn and 26.4 g/t Ag) is located in the Erenhot-East Ujimqin polymetallic metallogenic belt, on the western part of the Great Xing’an Range, Inner Mongolia, northeast China. The Ag-Pb-Zn mineralization mainly occurs as vein type ores hosted in argillaceous siltstone, feldspar quartz sandstone with silty slate interlayers of the Aobaotinghundi Formation of Lower Devonian. The hydrothermal ore-forming process can be divided into three stages, i.e., quartz–pyrite–arsenopyrite stage (I), quartz–polymetallic sulfides stage (II), and quartz–calcite–fluorite stage (III). Four types of fluid inclusions have been identified in the quartz-bearing veins of each stage, i.e., liquid-rich two-phase (L-type), single liquid-phase (PW-type), vapor-rich two-phase (V-type), and pure vapor phase (PV-type) inclusions. The fluid inclusions of stage I to III yield homogenization temperatures of 285–407 °C, 202–317 °C, and 144–239 °C, with salinities of 1.2–9.2 wt% NaCl equiv., 0.9–5.0 wt% NaCl equiv., and 0.2–2.6 wt% NaCl equiv., respectively. The ore-forming fluids at Hardat Tolgoi are characterized by moderate temperatures, low salinities, and low densities, and dominated by the H2O–NaCl system. Carbon and oxygen isotope compositions of calcite demonstrate that the ore-forming fluids come from a primary magmatic-hydrothermal system, with subsequent involvement of meteoric water at a later stage. Sulfur isotope analyses of sulfides yield δ34SV-CDT values of 1.8 to 8.7‰, with calculated δ34SH2S values of 1.4 to 9.4‰. The 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb ratios of sulfides range from 18.141 to 18.468, 15.521 to 15.617, and 38.040 to 38.377, respectively, similar to those of granites from the Hardat Tolgoi deposit. Both sulfur and lead isotope data indicate that the ore-forming metals were most likely derived from the magmatic reservoirs and sedimentary country rocks. The available fluid inclusion results and isotope studies indicate that the pahse separation, temperature decrease, and fluid mixing resulted in large-scale Ag-Pb-Zn ore formation at Hardat Tolgoi.

Genesis of the Mingsai Au deposit, southern Tibet: Constraints from geology, fluid inclusions, 40Ar/39Ar geochronology, H–O isotopes, and in situ sulfur isotope compositions of pyrite

Mingsai is a newly discovered Au deposit located in the eastern part of the Tethys Himalayan Au–Sb polymetallic metallogenic belt. The stratiform and lenticular orebodies are hosted within Middle Jurassic metamorphic tuff and quartz-sericite veins and controlled by an interlayer-gliding fracture zone with extensive hydrothermal alteration. In this study, at least three alteration/mineralization stages of the deposit were recognized as follows: (1) pre-ore stage (Stage Ⅰ), forming mainly ore-barren fine quartz veins without sulfides; (2) main ore stage (Stage Ⅱ), forming mainly thick quartz veins with abundant coarse-grained or fine-grained euhedraland subhedral Au-bearing pyrite, arsenopyrite and sericite; and (3) post-ore stage (Stage III), which is characterized by formation of thick barren quartz–calcite veins with few sulfides. Three types of fluid inclusions were identified as follows: (1) pure carbonic (V-type) inclusions, (2) aqueous-carbonic (C-type, including three-phase C1-type and two-phase C2-type) inclusions and (3) aqueous (L-type) inclusions. Fluid inclusions during the pre-ore stage are mainly C1-type, C2-type and V-type. The main ore stage contains mainly C1-type, C2-type, L-type and limited V-type, whereas the post-ore stage contains mainly L-type (with limited C2-type) fluid inclusions. From stages Ⅰ to III, microthermometric data show homogenization temperatures of 292–362 °C (mean = 309 °C), 247–320 °C (mean = 285 °C), and 206–272 °C (mean = 244 °C), respectively, and fluids with salinities of 0.2–8.3 (mean = 2.8) wt% NaCl equiv., 0.2–13.1 (mean = 5.8) wt% NaCl equiv., and 0.8–15.2 (mean = 8.3) wt% NaCl equiv., respectively. The δD values of the fluids from stages I to III range from −129.1‰ to −131.8‰, −137.5‰ to −137.4‰, and −143.6‰ to −138.6‰, respectively. The δ18OH2O values of the fluids from stages Ⅰ to III range from 13.3‰ to 13.6‰, 13.0‰ to 13.2‰, and 11.0‰ to 11.9‰, respectively. The δD and δ18OH2O values may reflect meteoric water involvement in ore-forming fluidssourced from either crustal metamorphism or mantle devolatilization. Fluid mixing is the crucial mechanism that controlled the deposition of the Au-bearing sulfides. In situ δ34S values of the Au-bearing pyrite range from 1.06‰ to 2.41‰, whereas δ34S values of the barren pyrite from the slate range from 8.19‰ to 15.86‰, indicating that sulfur of the Au-bearing pyrite has a deep source. The 40Ar–39Ar plateau age of hydrothermal ore-bearing sericite from the main ore stage is 16.03 ± 0.31 Ma, indicating that the mineralization time of the deposit is Miocene, which is different from other major gold deposits (Eocene) in the Tethys Himalayan Au–Sb polymetallic metallogenic belt. Consequently, taking the data together, it is suggested that the Mingsai is an orogenic-type Au deposit in the Tethys Himalayan Au–Sb polymetallic metallogenic belt.

Mineral chemistry and sources of fluid and sulfur at the Katbasu gold deposit in South Tianshan, NW China

Katbasu is a gold (and copper) deposit located in an arc on the southern margin of the Ili-Central Tianshan micro-continent. An in-situ method was conducted to acquire trace element concentrations to elucidate the origins and chemistry of the fluid in the Katbasu deposit. This included oxygen isotopes in quartz, as well as sulfur isotopes and trace elements concentrations in pyrite. Trace elements in gold deficient veins have higher concentrations compared to those in the gold bearing veins. The δ18O values of gold deficient veins are between 3.9 and 8.1‰, which imply a magmatic oxygen isotope signature. In contrast, oxygen isotopes in gold bearing veins range between −1.3 and 5.8‰, indicating the involvement of meteoric water in the mineralization system. This data, combined with evidence from alteration style and metal assemblages, shows that the ore-forming fluids at the Katbasu gold deposit is of a magmatic origin. The data also indicates that meteoric water diluted the magmatic fluid and caused an oversaturation of gold, causing precipitation of native gold grains. Trace elements in pyrite show no difference among the veins analyzed. However, they have distinctly different trace element patterns of pyrite from orogenic gold deposits. Based on the δ34S values of pyrite (8.3–12.9‰), and the lack of coeval regional metamorphism, we conclude that the enriched 34S at the Katbasu gold deposit is derived from a subducted slab during the Late Carboniferous.