Search Results (42)

The Xifanping Cu–(Au) deposit, a small-scale porphyry system in the central Jinshajiang–Red River tectonic belt (JSRR), formed in a Cenozoic collisional setting. This study integrates zircon U–Pb geochronology, Lu–Hf isotopes, whole-rock geochemistry, and zircon trace element analyses of ore-bearing and barren porphyries, combined with regional comparisons, to constrain magma sources, metallogenic controls, and genetic processes. Ore-bearing biotite quartz monzonite porphyries were emplaced at 32.15 ± 0.43 Ma and 32.49 ± 0.57 Ma, post-dating barren quartz monzonite porphyry (33.15 ± 0.51 Ma). These ages are consistent with molybdenite Re–Os ages (32.1 ± 1.6 Ma), indicating near-synchronous magmatism and mineralization. Both porphyry types belong to the shoshonitic, peraluminous series, enriched in LILE, depleted in HFSE, enriched in LREE, and lacking significant Eu anomalies. Their εHf (t) values (–2.94 to +3.68) and crustal model ages (TDM2 = 0.88–1.30 Ga) indicate derivation from Neoproterozoic subduction-modified lower crust. Ore-bearing porphyries, however, exhibit higher zircon Ce⁴⁺/Ce³⁺ ratios (average = 584 vs. 228 for barren porphyries) and elevated hydrous mineral contents (>10 vol.% amphibole + biotite), indicating more oxidized and water-rich parental magmas. Compared with large-scale porphyry systems (e.g., Dexing, northern Chile), the absence of adakitic signatures and only moderate oxidation limited the scale of mineralization. Overall, the Xifanping deposit formed through partial melting of Neoproterozoic subduction-modified lower crust in a post-collisional extensional regime: at ~33.2 Ma, melting of metasomatized ancient lower crust generated barren porphyries; at ~32 Ma, further evolution and differentiation of this lower crust magmas led to the extraction and enrichment of ore-forming materials from the thicken lower crust, producing hydrated, oxidized, ore-bearing magmas that intruded at shallow levels to form base and precious metal mineralizations. These results underscore the distinctive metallogenic characteristics of small-scale porphyry systems in collisional settings and provide new insights into how source composition and magma oxidation state constrain mineralization potential. Full article

Metabolic dysfunction-associated steatotic liver disease (MASLD) has emerged as the most prevalent chronic hepatopathy and a leading precursor of hepatocellular carcinoma (HCC) worldwide. Initially attributed to insulin resistance (IR)-driven metabolic imbalance, recent insights highlight a multifactorial pathogenesis involving oxidative stress (OS), chronic inflammation, and immune dysregulation. The hepatic accumulation of free fatty acids (FFAs) initiates mitochondrial dysfunction and excessive reactive oxygen species (ROS) production, culminating in lipotoxic intermediates and mitochondrial DNA damage. These damage-associated molecular patterns (DAMPs), together with gut-derived pathogen-associated molecular patterns (PAMPs), activate innate immune cells and amplify cytokine-mediated inflammation. Kupffer cell activation further exacerbates OS, while ROS-induced transcriptional pathways perpetuate inflammatory gene expression. Traditional immunity refers to the well-established dichotomy of innate and adaptive immune responses, where innate immunity provides immediate but non-specific defense, and adaptive immunity offers long-lasting, antigen-specific protection. However, a paradigm shift has occurred with the recognition of trained immunity (TI)—an adaptive-like memory response within innate immune cells that enables enhanced responses upon re-exposure to stimuli. Following non-specific antigenic stimulation, TI induces durable epigenetic and metabolic reprogramming, leading to heightened inflammatory responses and altered functional phenotypes. These rewired cells acquire the capacity to produce lipid mediators, cytokines, and matrix-modifying enzymes, reinforcing hepatic inflammation and fibrogenesis. In this context, the concept of immunometabolism has gained prominence, linking metabolic rewiring with immune dysfunction. This literature review provides an up-to-date synthesis of emerging evidence on immunometabolism and trained immunity as pathogenic drivers in MASLD. We discuss their roles in the transition from hepatic steatosis to steatohepatitis, fibrosis, and cirrhosis, and explore their contribution to the initiation and progression of MASLD-related HCC. Understanding these processes may reveal novel immunometabolic targets for therapeutic intervention. Full article

This study explores the magmatic and hydrothermal evolution of porphyry–skarn–transitional Cu-Mo-W-Au systems within the Nilüfer Mineralization Complex (NMC), located in the westernmost segment of the Eocene Tavşanlı Metallogenic Belt, NW Türkiye. Through integration of field data, whole-rock geochemistry, Re–Os molybdenite dating, and amphibole–biotite mineral chemistry, the petrogenetic controls on mineralization across four spatially associated mineralized regions (Kirazgedik, Güneybudaklar, Kozbudaklar, and Delice) were examined. The earliest and thermally most distinct phase is represented by the Kirazgedik porphyry system, characterized by high temperature (~930 °C), oxidized quartz monzodioritic intrusions emplaced at ~2.7 kbar. Rising fO₂ and volatile enrichment during magma ascent facilitated structurally focused Cu-Mo mineralization. At Güneybudaklar, Re–Os geochronology yields an age of ~49.9 Ma, linking Mo- and W-rich mineralization to a transitional porphyry–skarn environment developed under moderately oxidized (ΔFMQ + 1.8 to +0.5) and hydrous (up to 7 wt.% H₂O) magmatic conditions. Kozbudaklar represents a more reduced, volatile-poor skarn system, leading to Mo-enriched scheelite mineralization typical of late-stage W-skarns. The Delice system, developed at the contact of felsic cupolas and carbonates, records the broadest range of redox and fluid compositions. Mixed oxidized–reduced fluid signatures and intense fluid–rock interaction reflect complex, multistage fluid evolution involving both magmatic and external inputs. Geochemical and mineralogical trends—from increasing silica and Rb to decreasing Sr and V—trace a systematic evolution from mantle-derived to felsic, volatile-rich magmas. Structurally, mineralization is controlled by oblique fault zones that localize magma emplacement and hydrothermal flow. These findings support a unified genetic model in which porphyry and skarn mineralization styles evolved continuously from multiphase magmatic systems during syn-to-post-subduction processes, offering implications for exploration models in the Western Tethyan domain. Full article

The Chagai porphyry copper belt is a major component of the Tethyan metallogenic domain, which spans approximately 300 km and hosts several giant porphyry copper deposits. The tectonic setting, whether subduction-related or post-collisional, and the deep dynamic processes governing the formation of these giant deposits remain poorly understood. Mafic microgranular enclaves (MMEs), mafic dikes, and multiple porphyries have been documented in the Saindak mining area. This work examines both the ore-rich and non-ore intrusions in the Saindak porphyry Cu-Au deposit, using methods like molybdenite Re-Os dating, U-Pb zircon ages, Hf isotopes, and bulk-rock geochemical data. Geochronological results indicate that ore-fertile and barren porphyries yield ages of 22.15 ± 0.22 Ma and 22.21 ± 0.33 Ma, respectively. Both MMEs and mafic dikes have zircons with nearly identical ²⁰⁶Pb/²³⁸U weighted mean ages (21.21 ± 0.18 Ma and 21.21 ± 0.16 Ma, respectively), corresponding to the age of the host rock. Geochemical and Sr–Nd–Hf isotopic evidence indicates that the Saindak adakites were generated by the subduction of the Arabian oceanic lithosphere under the Eurasian plate, rather than through continental collision. The adakites were mainly formed by the partial melting of a metasomatized mantle wedge, induced by fluids from the dehydrating subducting slab, with minor input from subducted sediments and later crust–mantle interactions during magma ascent. We conclude that shallow subduction of the Arabian plate during the Oligocene–Miocene may have increased the flow of subducted fluids into the sub-arc mantle source of the Chagai arc. This process may have facilitated the widespread deposition of porphyry copper and copper–gold mineralization in the region. Full article

The Xulaojiugou Pb–Zn deposit, situated in the eastern Xing’an-Mongolia Orogenic Belt (XMOB), represents a medium-scale Pb–Zn deposit in central Heilongjiang Province, NE China. The mineralization occurs mainly near the contact zone of porphyritic biotite granite, medium-grained monzogranite, and marble in the Early Cambrian Qianshan Formation. Orebodies exhibit typical skarn characteristics and are structurally controlled by NE trending faults. To constrain the metallogenic age, ore-forming processes, and sources of ore-forming materials, we conducted integrated geochemical analyses, Re–Os isotope dating, in situ sulfur isotope analysis, and trace element analysis. Five molybdenite samples provided a Re–Os isochron age of 184.6 ± 3.0 Ma, indicating Early Jurassic mineralization. In situ δ³⁴S values from 20 sphalerite and 9 galena samples ranged from 5.31‰ to 5.83‰, suggesting derivation of sulfur from a deep magmatic source. Trace element analysis of 42 spots from three sphalerite samples revealed formation temperatures of 248–262 °C, which are consistent with mesothermal conditions. Integrated with regional tectonic evolution, the Xulaojiugou deposit is genetically linked to medium-grained monzogranite emplacement and represents a typical skarn polymetallic deposit, which is genetically associated with the regional porphyry–skarn metallogenic system that developed during the Early Yanshanian (Jurassic) tectonic–magmatic event and was driven by the subduction of the Paleo-Pacific plate. Full article

The Jinjingzui gold (Au) deposit is located in the central part of Edong, China. The theoretical gold reserves are large with significant potential for mining and future development. This deposit is the only Au-bearing deposit discovered in the Middle-Lower Yangtze River Valley Metallogenic Belt, which has existing ore bodies that are mainly diorite. Re–Os dating of molybdenite from the Jinjingzui deposit confirm that the deposit formed in the Lower Cretaceous period, with an isochron age of 138.5 ± 2.7 Ma. The geochemical data of the rocks indicate that the diorite contains 54.75% to 56.66% SiO₂, 5.68% to 8.94% Fe₂O₃, 2.05% to 2.19% MgO, and 1.06% to 1.08% TiO₂, and with enrichment of large-ion lithophile elements (e.g., Rb and Ba). High-field-strength elements U-Nb–Ti displayed strong negative anomalies. Six pyrites from the Jinjingzui Au deposit δ³⁴S_V-PDB(‰) ranged from −2.4% to −8.4%, with an average value of −3.1%, and ²⁰⁶Pb~²⁰⁴Pb, ²⁰⁷Pb~²⁰⁴Pb, ²⁰⁸Pb~²⁰⁴Pb contents ranged from 17.77–18.58, 15.48–15.67 to 37.91–39.05, with average values of 18.14, 15.59 and 38.49, respectively. These values indicate that the metallic components originated from the upper mantle and lower crust. The Re concentrations in the molybdenites are significantly higher than those in other ores within the district (847.91~2018.58 × 10⁻⁶), suggesting a significant mantle component was involved in the mineralization process. Full article

The oxime group is important in organic and inorganic chemistry. In most cases, this group is part of an organic molecule possessing one or more donor sites capable of forming bonds to metal ions. One family of such compounds is the group of 2-pyridyl (aldo)ketoximes. Metal complexes of 2-pyridyl oximes continue to attract the intense interest of many inorganic chemistry groups around the world for a variety of reasons, including their interesting structures, physical and biological properties, and applications. A unique member of 2-pyridyl ketoximes is di-2-pyridyl ketoxime (dpkoxH), which contains two 2-pyridyl groups and an oxime functionality that can be easily deprotonated giving the deprotonated ligand (dpkox⁻). The extra 2-pyridyl site confers a remarkable flexibility resulting in metal complexes with exciting structural and reactivity features. Our and other research groups have prepared and characterized many metal complexes of dpkoxH and dpkox⁻ over the past 30 years or so. This work is an attempt to build a “periodic table” of dpkoxH, which is near completion. The filled spaces of this “periodic table” contain metal ions whose dpkoxH/dpkox⁻ complexes have been structurally characterized. This work reviews comprehensively the to-date published coordination chemistry of dpkoxH with emphasis on the syntheses, reactivity, relationship to metallacrown chemistry, structures, and properties of the metal complexes; selected unpublished results from our group are also reported. The sixteen coordination modes adopted by dpkoxH and dpkox⁻ have provided access to monomeric and dimeric complexes, trinuclear, tetranuclear, pentanuclear, hexanuclear, heptanuclear, enneanuclear, and decanuclear clusters, as well as to a small number of 1D coordination polymers. With few exceptions ({M^IILn^III₂} and {Ni^II₂Mn^III₂}; M = Ni, Cu, Pd, and Ln = lanthanoid), most complexes are homometallic. The metals whose ions have yielded complexes with dpkoxH and dpkox⁻ are Cr, Mn, Fe, Co, Ni, Cu, Zn, Ru, Rh, Pd, Ag, Cd, Re, Os, Ir, Au, Hg, lanthanoids (mainly Pr and Nd), and U. Most metal complexes are homovalent, but some mixed-valence Mn, Fe, and Co compounds have been studied. Metal ion-assisted/promoted transformations of dpkoxH, i.e., reactivity patterns of the coordinated ligand, are also critically discussed. Some perspectives concerning the coordination chemistry of dpkoxH and research work for the future are outlined. Full article

The 1500 km-long Gangdese magmatic belt is a crucial region for copper polymetallic mineralization, offering valuable insights into collisional porphyry copper systems. This study focuses on the Demingding deposit, a newly identified occurrence of molybdenum–copper (Mo-Cu) mineralization within the eastern segment of the belt. While the mineralization age, magmatic characteristics, and tectonic context are still under investigation, we examine the deposit’s petrology, zircon U-Pb geochronology, whole-rock chemistry, and Re-Os isotopic data. The Demingding deposit exhibits a typical alteration zoning, transitioning from an inner potassic zone to an outer propylitic zone, which is significantly overprinted by phyllic alteration closely associated with Mo and Cu mineralization. Zircon U-Pb dating of the ore-forming monzogranite porphyries reveals crystallization ages ranging from 21 to 19 Ma, which is indistinguishable within error from the mean Re-Os age of 21.3 ± 0.4 Ma for Mo veins and veinlets hosted by these porphyries. This alignment suggests a late Miocene magmatic event characterized by Mo-dominated mineralization, coinciding with the continuous thickening of the continental crust during the collision of the Indian and Asian continents. The ore-forming porphyries range in composition from granodiorite to monzogranite and are classified as high-K calc-alkaline with adakite-like features, primarily resulting from the partial melting of subduction-modified thickened mafic lower crust. Notably, the ore-forming porphyries exhibit higher fO₂ and H₂O levels than barren porphyries in this area during crustal thickening, highlighting the significant contributions of hydrous and oxidized fluids from their source to the Mo-Cu mineralization process. Regional data indicate that the Gangdese porphyry metallogenic belt experienced concentrated Cu-Mo mineralization between 17 and 13 Ma. The formation of Mo-dominated deposits such as Demingding and Tangbula in the eastern segment of the belt, with slightly older ages around 20 Ma, underscores the presence of a significant porphyry Mo metallogenic event during this critical post-collision mineralization period. Full article

Background: To date, the only potential curative treatment for multiple myeloma (MM) remains allogeneic (allo) hematopoietic cell transplant (HCT), although, most patients will eventually relapse. In relapsed patients, donor lymphocyte infusions (DLIs) have been reported to control disease, but the optimal strategy prior to and doses of DLIs remain unclear. With this study (NCT03413800), we aimed to investigate the efficacy and toxicity of lenalidomide and dexamethasome (Len/Dex) followed by escalating pre-determined doses of DLIs in MM patients who relapsed after allo HCT. Methods: Patients aged 18–65 years with relapsed MM following upfront tandem autologous (auto)/allo HCT were eligible. Treatment consisted of six cycles of Len/Dex followed by three standardized doses of DLIs: 5 × 10⁶ CD3+/kg, 1 × 10⁷/kg and 5 × 10⁷/kg every 6 weeks. Bone marrow minimal measurable disease (MRD) using flow cytometry (10⁻⁵) was performed at enrolment, then every 3 months for 2 years or until disease progression, in a subset of patients. The primary endpoint was efficacy as measured by progression-free survival (PFS) at 2 years following Len/Dex/DLIs. Secondary objectives were safety including GVHD, response including MRD status and overall survival (OS). Results: A total of 22 patients participated in this study, including 62% with high-risk cytogenetics. With a median follow-up of 5.3 years (range: 4.1–6.1), PFS and OS were 26.5% (95% CI: 10.4–45.9%) and 69.2% (95% CI: 43.3–85.1%), respectively. Overall, the best responses achieved post-Len/Dex + DLIs were complete remission in 9.1%, very good partial response in 50%, and progressive disease in 40.9%. Among the nine patients tested for MRD, only two achieved a negative status after receiving DLIs. Six patients died, all due to disease progression. No acute GVHD was observed after DLIs. We report a very low incidence of moderate/severe chronic GVHD of 18.2% with no need for systemic immunosuppressants one year after diagnosis. No unexpected adverse events were observed. Interestingly, a positive correlation between response to Len/Dex re-induction and response to DLIs was found (p = 0.0032). Conclusions: Our findings suggest that Len/Dex/DLIs in second line treatment after upfront tandem auto/allo HCT in relapsed MM patients remains feasible and safe. With a potential correlation between induction chemotherapy and DLI responses, more potent induction regimens together with higher doses of DLIs should be considered in the future. Full article

The Songpan–Ganzi Orogenic Belt (SGOB) is bounded by the South China, North China, and Qiangtang blocks and forms the eastern margin of the Tibetan Plateau. The Tiechanghe Granite is located at the junction of the southeast margin of the SGOB and the western margin of the Yangtze Block. To elucidate the genetic relationship between the Tiechanghe Granite and the surrounding molybdenum deposits in Western Sichuan, in this study, we conducted zircon U-Pb and molybdenite Re-Os isotopic dating. The results indicate that the Tiechanghe Granite predominantly consists of monzogranite, with minor occurrences of syenogranite, while the molybdenum deposits are mainly found in skarn and quartz veins. The laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) zircon U-Pb ages of the Tiechanghe Granite range from 162.9 ± 0.7 Ma (MSWD = 0.31, n = 25) to 163.4 ± 0.6 Ma (MSWD = 0.85, n = 26), and the LA-ICP-MS zircon U-Pb age of the pegmatite veins is 164.1 ± 0.9 Ma (MSWD = 1.3, n = 19). These ages are consistent with the weighted average Re-Os age of the Ziershi molybdenite (160.3 ± 1.6 Ma, n = 2) within the error margins. These findings and previously obtained magmatic and metallogenic ages for the region suggest that a magmatic and mineralization event involving granite, molybdenum, tungsten, and copper occurred at around 162–164 Ma in the study area. This discovery broadens the exploration perspective for mineral resources in the Jiulong area of Western Sichuan and the entirety of Western Sichuan. Full article

The northern margin of the North China Craton is one of the most important porphyry-skarn molybdenum ore belts in the world. The eastern Hebei Province, which contains a high number of molybdenum and gold (molybdenum) resources, is an important portion of the northern margin of the North China Craton. Xichanggou and Huashi, located in eastern Hebei, are quartz-molybdenum vein deposits that are intimately associated with intrusions that are deeply concealed in the mining area. This work presents two zircon U-Pb dates and ten molybdenite Re-Os ages from samples of the aforementioned two deposits in order to determine the timing of the intrusion and mineralization. The zircon U-Pb ages of the quartz monzonite porphyry from Xichanggou are determined to be 163.3 ± 0.3 Ma and 162.8 ± 0.4 Ma. The molybdenite Re-Os dating yielded ages of 160.3 ± 4.6 Ma for Xichanggou and 171.4 ± 19 Ma for Huashi, respectively. The isotopic composition of oxygen and hydrogen of the ore-forming fluid from Huashi, as indicated by the δD_V-SMOW values (−80.0‰ to −67.6‰) and δ¹⁸O_H2O values (−1.86‰ to 2.33‰), suggests that the fluid is primarily composed of water derived from magma, with some contribution from atmospheric precipitation. The sulfur isotope values (δ³⁴S) of sulfides from Xichanggou range from 6.5‰ to 7.1‰, while the δ³⁴S values from Huashi range from 3.3‰ to 4.9‰. The lead isotope ratios (²⁰⁶Pb/²⁰⁴Pb and ²⁰⁷Pb/²⁰⁴Pb) of sulfides from Xichanggou and Huashi average at 17.414, 15.428, and 17.591, 15.379, respectively. The Re-Os isotopic compositions of ore sulfides mostly fall within the range of 318 ppm to 50,114 ppm. These isotopic compositions indicate that the materials responsible for the formation of the ores in Xichanggou and Huashi primarily originate from the melting of lower crust materials that have been contaminated by the mantle. Based on the regional data, the molybdenum deposits in eastern Hebei were formed in multiple periods, specifically approximately 170 Ma and 160 Ma in Huahsi and Xichanggou, respectively. The subduction of the Paleo-Pacific plate during the middle–late Jurassic period led to the partial remelting of lower crust material, resulting in the acquisition of a significant quantity of metal elements (Mo), which were subsequently deposited. Full article

The Yuhaixi Mo(Cu) deposit is a new discovery in the eastern section of the Dananhu-Tousuquan island arc, Eastern Tianshan. However, the genesis of the Yuhaixi Mo(Cu) deposit is still not fully understood. The Yuhaixi intrusion is composed of monzonitic granites, diorites, granites, and gabbro dikes, among which disseminated or veinlet Mo and Cu mineralization is mainly hosted by the monzonitic granites. The LA-ICP-MS zircon U-Pb dating yields emplacement ages of 359.4 ± 1.6 Ma for the monzonitic granite, 298.8 ± 1.8 Ma for the diorite, and 307.0 ± 2.3 Ma for the granite. The Re-Os dating of molybdenite hosted by monzonitic granite yields a well-constrained ¹⁸⁷Re-¹⁸⁷Os isochron age of 354.1 ± 6.8 Ma (MSWD = 1.7) with a weighted average age of 344.5 ± 3.1 Ma. The Mo mineralization is closely associated with the Yuhaixi monzonitic granite. The Yuhaixi monzonitic granite rocks are characterized by high silica (SiO₂ > 70 wt.%), low MgO (0.23–0.36), Ni, Cr contents, and they are enriched in light rare earth elements (LREEs) and large ion lithophile elements (LILEs: e.g., K, Ba, Pb and Sr), and depleted in heavy rare earth elements (HREEs) and high field-strength elements (HFSEs: e.g., Nb, Ta and Ti). They are weak peraluminous and have high εHf(t) (11.37–17.59) and εNd(t) (1.36–7.75) values, and varied initial ⁸⁷Sr/⁸⁶Sr (0.7037–0.7128) values. The Yuhaixi post-ore granites exhibit similar geochemical and isotopic signatures to the Yuhaixi monzonitic granite. These characteristics suggest that the Yuhaixi felsic rocks are likely sourced from the partial melting of the juvenile lower crust. The Yuhaixi diorite has low SiO₂, and K₂O contents, relatively high Na₂O, MgO (Mg^# = 45–53) contents, and depletions in HFSE (e.g., Nb, Ta, and Ti). These geochemical features, coupled with isotopic data such as low initial ⁸⁷Sr/⁸⁶Sr (≤0.7043), high εNd(t) (2.5 to 3.0) and εHf(t) (≥11.6) values, and young Hf model ages, suggest that their parental magmas possibly originated from the partial melting of the depleted lithospheric mantle that was metasomatized by hydrous melts or fluids from the subducting oceanic plate. Integrating our new results with previous works on the Dananhu-Tousuquan island arc belt, we suggest that the Yuhaixi Mo(Cu)deposit is likely sourced from the juvenile lower crust, which was formed in an arc setting, where the bipolar subduction of the North Tianshan oceanic slab forms the Dananhu Tousuquan belt to the north and the Aqishan-Yamansu belt to the south. The eastern section of the Dananhu-Tousuquan island arc is a promising target for late Paleozoic porphyry Mo(Cu) deposits. Full article

The Lower Urgen molybdenum deposit (44,856 t Mo @ 0.141%), situated in the northern Great Xing’an Range, is a newly discovered porphyry molybdenum deposit. Mineralization is characterized by veinlet-disseminated- and vein-type quartz–sulfide orebodies primarily occurring in the cupola of the Early Cretaceous granite porphyry stock. In this study, we present a detailed description of the ore geology, molybdenite Re-Os dating, H-O-S-Pb isotopic compositions, and fluid inclusion (FI) analyses including petrography, laser Raman, and microthermometry to precisely constrain the timing of ore formation, the origin of ore-forming fluids and materials, as well as the metal precipitation mechanism. Molybdenite Re-Os dating yielded two model ages of 141.2 ± 1.5 and 147.7 ± 1.7 Ma, coeval with the regional Late Jurassic–Early Cretaceous molybdenum metallogenesis. The hydrothermal process can be divided into three stages: the quartz–molybdenite(–pyrite) stage, quartz–polymetallic sulfide stage, and quartz–carbonate stage. Four types of FIs were distinguished for quartz, including two-phase liquid-rich (L-type), saline (S-type), CO₂-rich (C1-type), and CO₂-bearing (C2-type) FIs. Microthermometric data showed that the homogenization temperatures and salinities from the early to late stages were 240–430 °C, 5.0–11.9, and 30.1–50.8 wt% NaCl equiv.; 180–280 °C and 3.0–9.1 wt% NaCl equiv.; and 120–220 °C and 0.2–7.9 wt% NaCl equiv., respectively, suggesting a decreasing trend. H-O isotopic compositions indicate that the ore-forming fluids were initially of magmatic origin with the increasing incorporation of meteoric water. S-Pb isotopic compositions indicate that the ore-forming materials originated from granitic magmas, and the mineralization is genetically related to the ore-bearing granite porphyry stock in the deposit. Fluid immiscibility and fluid–rock interaction are collectively responsible for the massive deposition of molybdenite in stage 1, whereas fluid mixing and immiscibility played a critical role in the deposition of polymetallic sulfide in stage 2. Full article

The Xiongcun Cu–Au ore district is in the southern middle Gangdese Metallogenic Belt, Tibet, and formed during Neo-Tethyan oceanic subduction. The Xiongcun ore district mainly comprises two deposits, the No. I and No. II deposits, which were formed by two individual mineralization events according to deposit geology and Re–Os isotopic dating of molybdenite. The No. I deposit is similar to a reduced porphyry copper–gold deposit, given the widespread occurrence of primary and/or hydrothermal pyrrhotite and common CH₄-rich and rare N₂-rich fluid inclusions. The No. II deposit, similar to classic oxidized porphyry copper–gold deposits, contains highly oxidized minerals, including magnetite, anhydrite, and hematite. The halogen chemistry of the ore-forming fluid from the No. I and No. II deposits is still unclear. Biotite geochemistry with halogen contents was used to investigate the differences in ore-forming fluid between the No. I and No. II deposits. Hydrothermal biotite from the No. I deposit, usually intergrown with sphalerite, is Mg-rich and classified as phlogopite and Mg-biotite, and hydrothermal biotite from the No. II deposit is classified as Mg-biotite. Hydrothermal biotite from the No. I deposit has significantly higher SiO₂, MnO, MgO, F, Li, Sc, Zn, Rb, Tl, and Pb contents and lower Al₂O₃, FeO_tot, Cl, Ba, Cr, V, Co, Ni, Y, Sr, Zr, Th, and Cu contents than the biotite from the No. II deposit. Hydrothermal biotites from the No. I and No. II deposits yield temperatures ranging from 230 °C to 593 °C and 212 °C to 306 °C, respectively. The calculated oxygen fugacity and fugacity ratios indicate that the hydrothermal fluid of the No. I deposit has a higher F content, oxygen fugacity, and log(fHF/fHCl) value and a lower log(fH₂O/fHF) value than the hydrothermal fluid from the No. II deposit. The biotite geochemistry shows that the No. I and No. II deposits formed from different hydrothermal fluids. The hydrothermal fluid of the No. I deposit was mixed with meteoric waters containing organic matter, resulting in a decrease in oxygen fugacity and more efficient precipitation of gold. The No. I and No. II deposits were formed by a Cl-rich hydrothermal system conducive to transporting Cu and Au. The decreasing Cl, oxygen fugacity, and temperature may be the key factors in Cu and Au precipitation. Biotite geochemistry allows a more detailed evaluation of the halogen chemistry of hydrothermal fluids and their evolution within porphyry Cu systems. Full article

With the targets of petroleum exploration transferred to the deep and ancient strata, abundant oil and gas resources have been found in Lower Paleozoic and older strata in central and western China. Due to complex evolutionary processes including multiple episodes of hydrocarbon accumulation and ubiquitously accompanied by secondary alterations, significant uncertainties remain concerning the generation time and accumulation processes of these revealed petroleum sources. In this paper, relative pure Re and Os elements existing in the asphaltene fractions of Lower Cambrian solid bitumen collected from the Guangyuan area, western Sichuan Basin, SW China and Middle–Lower Ordovician heavy oils in the Aiding area of the Tahe oilfield in the Tarim Basin, NW China were successfully obtained by sample pretreatments, and Re–Os isotopic analysis was subsequently carried out for the dating of these. The Re–Os isotopic composition indicates a generation time of Guangyuan bitumen to between 572 Ma and 559 Ma, corresponding to the late Sinian period of the Neoproterozoic era. By the means of Re–Os isochron aging, initial ¹⁸⁷Os/¹⁸⁸Os ratios, and carbon isotopic compositions, the Lower Cambrian bitumen is supposed to originate from source rocks of the Doushantuo Formation in the Sinian strata and subsequently migrated into the reservoirs of the Dengying Formation. This previously reserved petroleum was transformed into its present bitumen state by the destruction of reservoirs caused by tectonic uplift. The Re–Os dating results of Middle–Lower Ordovician heavy oil of Tarim Basin suggest that it was formed between 450 Ma to 436 Ma, corresponding to the Late Ordovician–Early Silurian system, and the generated petroleum likely migrate into the Middle–Lower Ordovician karst reservoirs to form early oil reservoirs. With tectonic uplift, these oil reservoirs were degraded and reformed to the heavy-oil reservoirs of today. Full article