Search Results (166)

The Bastielieke W-polymetallic deposit, located in the Xinjiang Altay metallogenic belt, records a complex hydrothermal history critical to understanding multi-stage metallogenic processes in the southern Altay. This study integrates in situ U-Pb dating of hydrothermal titanite and zircon with textural and compositional analyses of titanite to reconstruct this history. Three types of hydrothermal titanite, identified from pyroxene skarn (TtnI), epidote skarn (TtnII), and quartz–sulfide ore (TtnIII), display dissolution–reprecipitation textures and systematic compositional variations, indicating distinct fluid compositions and origins. TtnI, TtnII, and TtnIII yield U-Pb ages of 244.7 ± 7.8 Ma, 252.4 ± 5.5 Ma, and 250.6 ± 3.0 Ma, respectively, and hydrothermal zircon from pyroxene skarn yields an age of 249.9 ± 2.1 Ma, constraining the hydrothermal event to the latest Permian to Early Triassic. These ages are interpreted to record the timing of U-Pb system resetting during regional shear–thrust movements. Compositional variations among the three titanite types reveal a two-stage hydrothermal history. The earlier stage involved W–Cu mineralization and protolith titanite precipitation related to magmatic–hydrothermal fluids exsolved from Permian granites. The later stage was driven by regional shear–thrust movements and metamorphic–hydrothermal processes, which reset the titanite U-Pb systems, partially altered TtnI and TtnII, precipitated TtnIII, and remobilized metals. This model links the Bastielieke deposit to multi-stage hydrothermal processes and provides insights into similar metallogenic events along the southern margin of Xinjiang Altay. Full article

The Nam Xan gold deposit is located in the central Truong Son Fold Belt of Laos. It is a newly identified distal intrusion-related gold system (IRGS) in a continental arc setting. This study uses whole-rock geochemistry, Pb and S isotope systematics, and mineral-scale analyses to trace magmatic evolution and ore-forming processes. Whole-rock data indicate that the associated intrusive suite is a calc-alkaline volcanic-arc granite (VAG) series, derived from a subduction-modified mantle source with notable crustal contributions. Pb isotopes reveal mixing arrays rather than true isochrons. Monte Carlo modeling shows binary mantle–crust mixing for igneous rocks and ternary mixing with an additional radiogenic component in ore samples, indicating enhanced fluid–rock interaction during mineralization. Sulfur isotope data show a shift from magmatic sulfur (δ³⁴S ≈ −5‰) in early skarn-stage pyrite to heavier values (δ³⁴S ≈ +6‰) in gold-bearing stages, reflecting fluid evolution driven by cooling and redox changes. Mineral chemistry data demonstrate that gold is present both as invisible gold within arsenian pyrite and as free gold in late-stage fractures. Strong correlations between Au and As, along with elevated Co/Ni ratios and enrichments in Bi, W, and F, collectively support a magmatic-hydrothermal origin. These findings define a three-stage mineralization process: an initial phase involving high-temperature magmatic fluids, a main stage characterized by sulfidation and gold deposition, and a final stage marked by polymetallic overprinting. The Nam Xan deposit is therefore interpreted as the distal manifestation of a Permian arc-related magmatic system in which magmatic fluids migrated along structural conduits and precipitated gold through interaction with carbonate host rocks. The identification of these intrusions in the distal IRGS at Nam Xan informs regional exploration models in the Truong Son Fold Belt, demonstrating the potential of carbonate platforms near Permian intrusions for future mineral exploration. Full article

The Dajing giant Cu–Sn polymetallic deposit is located in the Cu–Sn–Ag–Pb–Zn polymetallic belt of the southern Great Xing’an Range, NE China. Research on its ore genesis is of great significance for understanding Sn polymetallic mineralization in this region. In this study, pyrite, arsenopyrite, and sphalerite were analyzed by electron-microprobe analysis (EMPA) and in situ S–Pb isotope analysis. Previously published fluid-inclusion microthermometric and H–O isotope data were also incorporated to constrain fluid evolution and ore genesis. Both in situ S and Pb isotopic compositions fall within short ranges. The δ³⁴S values suggest a sulfur reservoir with possible magmatic contribution, whereas Pb isotopes indicate a mainly crustal Pb signature in an orogenic setting. Arsenopyrite records variations in As, S, Fe, and Co contents from core to rim. The Co-rich core shows Co enrichment accompanied by Fe depletion, consistent with Co-for-Fe isomorphous substitution. These features indicate changes in local fluid chemistry during arsenopyrite growth. Sulfur isotope geothermometry based on coexisting late-stage pyrite–sphalerite pairs yields 118–233 °C, with an average of 159 ± 49 °C, indicating medium- to low-temperature hydrothermal activity during the late sulfide stage. The Dajing deposit is interpreted as a fault-controlled hydrothermal vein-type Cu–Sn polymetallic deposit formed in a Late Jurassic extensional setting. Ore precipitation was likely promoted by cooling during upward fluid migration away from the magmatic heat source, pressure release, meteoric-water mixing, and fluid–rock interaction with granitic rocks and Linxi Formation wall rocks. This study provides mineral-scale constraints on fluid evolution and ore genesis in the Great Xing’an metallogenic belt. Full article

The Shizui Cu–Pb–Zn deposit is located in central Jilin Province. It sits at the tectonic junction between the eastern Xing’an–Mongolia Orogenic Belt (XMOB) and the northeastern North China Craton (NCC). This is the first discovered Paleozoic Cu-polymetallic deposit in the region. Our study combines detailed geological investigation with systematic fluid inclusion analysis. We analyzed samples from four distinct paragenetic stages. Analytical methods include microthermometry, laser Raman spectroscopy, and hydrogen-oxygen isotope analysis. These data constrain the source, evolution, and precipitation mechanisms of the ore-forming fluids. The results delineate a clear evolutionary path: the ore-forming fluid originated as a high-temperature (346–437 °C), high-salinity (up to 51.68 wt.% NaCl equiv.) NaCl–H₂O–CO₂ system during the early quartz-sulfide stage (Stage I, Quartz ± Arsenopyrite ± Pyrite Stage), as evidenced by the coeval presence of high-salinity S-type and CO₂-rich C-type inclusions, indicating fluid immiscibility. The fluid then evolved into a boiling, medium temperature to high temperature (262–355 °C), high-salinity NaCl–H₂O system during the later part of early quartz-sulfide stage (Stage II, Quartz-Cu Polymetallic Sulfide Stage), a transition marked by the common coexistence of liquid-rich (L-type) and vapor-rich (V-type) inclusions with similar homogenization temperatures. This phase separation (boiling) served as the primary trigger for the massive deposition of chalcopyrite, arsenopyrite, and pyrite. Subsequently, the system cooled and diluted, transforming into a medium- to low-temperature (182–275 °C), low-salinity, partially homogeneous NaCl–H₂O system in the late quartz-sulfide stage (Stage III, Quartz-Pb-Zn Polymetallic Sulfide Stage). Finally, in the quartz-carbonate stage (Stage IV, Quartz-Carbonate Stage), the fluid temperature further decreased, resulting in a low-temperature (128–211 °C), low-salinity, homogeneous NaCl–H₂O system. Hydrogen-oxygen isotope data show that the calculated δ¹⁸O_H2O values decreased from +6.6‰ to +6.7‰ in Stage I to +3.4‰ to +3.9‰ in Stage II, and further to −0.4‰ in Stage III, while the δD values shifted from −91.6‰ to −90.6‰, to −94.4‰ to −94.2‰, and finally to −95.7‰. This trend indicates that the initial magmatic fluid progressively mixed with meteoric water. The geological characteristics, spatial association with Hercynian biotite monzogranite, developed skarn alteration, and the documented fluid evolution trajectory collectively affirm that the Shizui deposit is a typical skarn-type system. The deposit shares significant similarities in mineralization conditions, age, and tectonic setting with the skarn-type Tianbaoshan Pb–Zn–Cu–Mo deposits in the western segment of the XarMoron–Changchun Metallogenic Belt (XCMB). This correlation strongly suggests that the Paleozoic XCMB extends eastward and holds considerable potential for the discovery of late Paleozoic skarn-type Cu-polymetallic deposits in its eastern part. Full article

The Liwu copper deposit, located on the western margin of the Yangtze Block, is a typical metamorphic-hosted polymetallic Cu deposit with significant deep exploration potential. To constrain its mineralization-forming processes and primary halo characteristics, this study focuses on the Heiniudong ore segment. Based on portable X-ray fluorescence (XRF) data obtained from drill cores and underground samples, a comprehensive geochemical analysis of 20 elements was conducted. Elemental background values and anomaly thresholds were determined using the iterative sigma (σ) elimination method. Pearson correlation analysis and hierarchical cluster analysis were applied to identify element associations, while the Grigorian zonation index method was employed to investigate axial zoning patterns of primary halos. The results demonstrate that Cu exhibits strong positive correlations with S, Fe, Ag, Cd, Sn, and Bi, indicating a medium- to high-temperature hydrothermal sulfide mineralization system. The primary halo displays well-defined vertical zonation, with Ba–Sr–Sb–As representing the front halo, Zn–Pb–Cu–Ag–Sn–Fe–Cd the near-ore halo, and Bi–Mo–W–Th the tail halo. A clear axial zonation sequence is established. The vertical variation in the geochemical ratio (As × Sr × Sb)/(Mo × Bi × W) exhibits a characteristic “low–high–low–high” pattern, reflecting the superposition of the front halo of a deeper concealed orebody with the tail halo of the upper known orebody under multistage hydrothermal remobilization and structural overprinting. Integrated with the coexistence of front halo and tail halo anomalies and strong alteration in drill hole WT03, the results indicate that the southwestern extension of WT03 along southwest-dipping ductile–brittle detachment structures represents the most promising deep exploration target. Full article

The increasing demand for high-purity lead sulfide (PbS) for optoelectronic applications necessitates efficient methods to remove residual antimony sulfide (Sb₂S₃) from complex ores—a challenge due to their chemical similarity and fine intergrowth. This study presents a hybrid purification strategy combining vacuum distillation pretreatment with oxygen-free alkaline selective leaching. Thermodynamic analysis using Eh-pH diagrams revealed significant differences in the behavior of trace Sb₂S₃ and bulk PbS under alkaline conditions (pH 9–11), identifying a suitable window for selective dissolution. The process begins with mechanical ball milling to break Sb₂S₃ inclusions and improve reaction kinetics, followed by anaerobic leaching in a sealed reactor under inert atmosphere using a NaOH solution at a controlled potential (Eh 0.1–0.35 V vs. SHE). Multiple characterization techniques confirmed that Sb₂S₃ undergoes dissolution and conversion while the PbS phase remains intact. Notably, zeta potential measurements (−12.3 mV) and high conductivity (204 mS/cm) indicated the formation of a stable colloidal dispersion system favorable for interfacial reactions. Under optimal conditions, antimony removal exceeded 99% with lead loss below 1%. Overall, the proposed strategy offers a technically viable route to produce ≥99.9% pure PbS from polymetallic sources, addressing a longstanding separation challenge. Full article

The Dongwujiiazi deposit is a structurally controlled orogenic gold deposit situated in the eastern part of the Chifeng–Chaoyang gold belt along the northern boundary of the North China Craton. This study establishes a comprehensive metallogenic model for the Dongwujiiazi gold deposit by integrating whole-rock geochemistry (major and trace elements), in situ trace elements and REEs in zircon, multi-isotope systems (H, O, S, Pb), and precise zircon U–Pb geochronology. Five types of intrusive and associated rocks are identified within the main biotite-pyroxene gneiss host of the Dongwujiiazi gold deposit: mylonitized granitic pegmatite, mylonitized porphyritic monzogranite, propylitized fine-grained quartz monzodiorite, quartz monzonite, and porphyritic dolerite. The gold-bearing polymetallic sulfide ores are composed of pyrite, chalcopyrite, sphalerite, galena, digenite, and native gold. Zircon grains in the Dongwujiiazi gold ore (2502 ± 15 to 2539 ± 18 Ma) are inherited from surrounding Neoarchean gneiss, recording older crustal sources rather than forming contemporaneously with the gold mineralization. H–O isotopes indicate that the ore-forming fluids were mixed in origin, involving both magmatic and metamorphic components. S and Pb isotopes suggest that the mineralizing sulfur was mainly derived from a magmatic source, while lead originated predominantly from lower crustal materials associated with the surrounding high-grade metamorphic rocks. In this study, we present a new metallogenic model for the Dongwujiiazi gold deposit, in which slab-derived and lower-crustal metamorphic fluids interacted with ascending magmas, resulting in fluid mixing and gold precipitation within structurally controlled zones of gneissic host rocks. Combined geochemical and isotopic evidence (H–O, S, Pb) indicates contributions from both magmatic and metamorphic sources, supporting formation as an intracontinental orogenic gold system in an active continental margin. Full article

The peripheries of rare-metal metallogenic systems frequently host skarn-type or hydrothermal vein-type Pb-Zn deposits, though their genetic connections with parental systems remain debated. The newly identified Gariatong W-Mo polymetallic metallogenic system in the Lhasa Terrane displays well-defined Nb-Ta-Rb, Mo-W, W-Mo, W-Bi, and Pb-Zn-Ag metallogenic zoning, establishing it as an exemplary site for investigating genetic relationships between Pb-Zn and rare-metal mineralization. This investigation targets skarn-type Pb-Zn deposits spatially associated with rare-metal orebodies at Gariatong, utilizing integrated analytical approaches, including in situ LA-ICP-MS trace-element analysis of sulfides, sulfur isotope geochemistry, and LA-ICP-MS elemental mapping of sphalerite, to constrain metal sources, characterize fluid evolution, and establish genetic correlations with the rare-metal system. Key findings include the following: (1) sphalerite shows enrichment in Fe, Mn, Co, and Cd, while pyrite contains elevated As, Pb, Co, Cu, and Mn. Fe, Cd, and Mn primarily occur as solid solutions or nanoparticles, whereas As and Pb exist as micro-inclusions. (2) Sphalerite Zn/Cd ratios (73.6–184) and Co-Ni-As ternary diagrams confirm a magmatic–hydrothermal skarn origin. (3) Mineralization occurred under moderate-temperature, mildly oxidized conditions, as constrained by sphalerite Fe contents and mineral assemblages. Sulfur isotope compositions (δ³⁴S = −1.0‰ to 3.2‰; mean: 1.9‰) indicate a magmatic sulfur source. This study reveals that the Nb-Ta-Rb mineralization, quartz-vein- and greisen-type W-Mo deposits, and skarn-type Pb-Zn orebodies—all genetically associated with highly fractionated granites—constitute an integrated magmatic–hydrothermal system with vertical (depth-related) zoning relative to the granitic intrusion. These results provide critical constraints for understanding rare-metal–Pb-Zn genetic associations and suggest that Pb-Zn mineralization may serve as a key exploration indicator for rare metals in the Lhasa Terrane. Full article

The Yechangping super-large porphyry–skarn deposit is a key component of the East Qinling molybdenum metallogenic belt, central China. Magnetite is widely developed across all mineralization stages of this deposit, yet its systematic geochemical evolution and prospecting significance remain poorly constrained. This study presents in situ major- and trace-element analyses of magnetite via electron probe microanalysis (EPMA), laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS), and elemental mapping, to unravel the ore-forming hydrothermal evolution and establish reliable prospecting indicators. Four magnetite generations are identified based on petrography and paragenetic relationships: late skarn stage (Mt1), oxide stage (Mt2 and Mt3), and polymetallic sulfide stage (Mt4). Magnetite has total iron contents (TFeO, total Fe calculated as FeO) of 82.72–95.46 wt.% (values above the 93 wt.% stoichiometric limit of pure magnetite stem from minor oxidation), with dominant isovalent Fe³⁺ and Al³⁺ lattice substitution supported by a significant negative Fe–Al correlation. Systematic stage-dependent geochemical variations are observed: Mt1 has the highest Ti (mostly >1500 ppm), V and Cr, while Mt2–Mt4 show progressive Ti depletion (mostly <100 ppm), recording continuous cooling of the hydro-thermal system. V and Cr contents decrease markedly from Mt1 to Mt3, with secondary enrichment in Mt4; Mo concentrations peak in Mt2 (average 5.06 ppm), coupled with elevated chalcophile metalloid Te, As, Pb and Bi. Elemental mapping results show that K occurs as discrete hotspots, which may be mainly derived from feldspar microinclusions, rather than lattice substitution in magnetite. These geochemical fingerprints record a transition from high-temperature magmatic–hydrothermal fluids to late contact-metasomatic fluids, with evolving fluid–rock interaction and oxygen fugacity. Our results demonstrate that magnetite chemistry is a reliable tool for discriminating mineralization stages and vectoring prospecting targets in porphyry–skarn Mo–W systems. Full article

Open-pit polymetallic mines commonly encounter challenges such as the asynchrony between mining and processing operations, large fluctuations in ore supply structure, and high haulage volumes, which lead to increased transportation costs and instability in processing plant feed grades. To address these issues, this study, driven by practical production requirements, proposes a two-stage hybrid optimization strategy that combines the global search capability of NSGA-III with the local intensification of particle swarm optimization (PSO), aiming to achieve the coordinated optimization of transportation cost minimization and plant feed grade maximization under constraints imposed by ore supply boundaries and processing plant capacity. To further identify the most suitable solution from the resulting Pareto-optimal set, the VIKOR multi-criteria decision-making method is employed to evaluate and select a blending scheme with optimal balance under the dual objectives of cost and grade. The effectiveness of the proposed approach is validated using a real-world production case, with experimental results showing that the optimized blending scheme achieves a cost reduction of more than 9%, while the gold grades of oxide and sulfide ores are increased to 2.40–3.16 g/t and 2.14–2.17 g/t, respectively, leading to a significant improvement in the overall plant feed grade. Compared with the actual weekly blending plan used in practice, the proposed method enables a comprehensive optimization of transportation cost, feed grade, and ore supply structure within a unified framework. Full article

The Xinqiao Cu-S polymetallic deposit is located in the Tongling ore concentration area of the Middle-Lower Yangtze River metallogenic belt. The orebodies consist of skarn orebodies and stratiform sulfide orebodies, but the genetic link between them remains controversial. In this study, magnetite was used as a proxy to systematically constrain the hydrothermal evolution from the intrusion to the contact zone and further to the stratiform orebodies. A representative drill hole (E603) was logged, and samples were systematically collected from the Jitou pluton outward to the contact zone. Composite samples from the 8–28 m interval were crushed and prepared as resin mounts for integrated TIMA automated mineralogy, BSE textural observation, and in situ LA-ICP-MS trace element analysis. Five types of magnetite (Mt1 to Mt5) were systematically identified. Mt1 occurs as inclusions within feldspar in the quartz monzodiorite. It exhibits typical magmatic magnetite characteristics and contains grid-like ilmenite exsolution, indicating crystallization during the late magmatic stage. Mt2 is distributed in the interstices of magmatic minerals, commonly showing hematitization and replacement of ilmenite exsolution lamellae by titanite. Its trace element geochemistry displays magmatic–hydrothermal transitional features. Mt3–Mt5 in the skarn and stratiform orebodies are paragenetic with retrograde alteration minerals (e.g., epidote, chlorite, and actinolite) and sulfides, and are characterized by low Ti, Al, and V contents and high Mg, Mn, and Sn contents, indicating a hydrothermal origin. From Mt3 to Mt5, (Ti + V) and (Al + Mn) decrease, while Zn and Mn increase, accompanied by a decrease in the (Si + Al)/(Mg + Mn) ratio. This reflects a trend of decreasing fluid temperature and progressively enhanced wall-rock buffering. The Mg-in-magnetite geothermometer yields relatively consistent results for Mt1–Mt3, but anomalously high temperatures for Mt4–Mt5. This suggests that the elevated Mg activity in the fluid, caused by reaction with carbonate wall rocks, can significantly influence the calculated temperatures. Therefore, this geothermometer should be used cautiously for magnetite in the outer skarn zone and interpreted in combination with other temperature constraints. The textures, paragenetic mineral assemblages, and trace element characteristics of magnetite collectively reveal a continuous mineralization process linking the skarn and stratiform orebodies at Xinqiao, providing robust mineralogical and geochemical evidence for the contribution of Yanshanian magmatic–hydrothermal activity to the stratiform mineralization. Full article

The physicochemical controls on gold precipitation in orogenic gold deposits remain poorly constrained, with traditional fluid inclusion and isotopic studies often yielding ambiguous results due to overprinting or incomplete records. This study addresses this challenge using chlorite—a sensitive mineral proxy for fluid conditions—as a quantitative sensor in the Jinshan orogenic gold deposit (>200 t Au) of the Jiangnan orogenic belt, South China. Hosted in Neoproterozoic phyllite within NE–NNE-trending ductile–brittle shear zones, Jinshan features auriferous quartz–polymetallic sulfide veins with prominent chlorite alteration. Integrating high-resolution SEM-EPMA analyses of multi-generational chlorite with thermodynamic modeling, we reconstruct the temporal evolution of temperature, oxygen fugacity (fO₂), pH and sulfur fugacity (fS₂) during ore formation. Four paragenetic stages are identified: Stage 1 (ankerite–quartz), Stage 2 (pyrite–arsenopyrite–quartz), Stage 3 (quartz–gold–polymetallic sulfide), and Stage 4 (chlorite–carbonate–quartz). Electron microprobe analysis reveals that the chlorite composition changes from Fe-rich chamosite (Stage 2) to Mg-rich clinochlore (Stage 3) and then to Fe-rich chamosite (Stage 4). Chlorite from Stage 2 (Chl-1) formed metasomatically at low fluid/rock ratios, while Stage 3 and 4 chlorites (Chl-2 and Chl-3) precipitated directly from higher fluid/rock ratio fluids. Chlorite compositions record a critical Stage 2–3 transition involving cooling from ~320 °C to ~260 °C, reduction (log fO₂ from −33.6 to −39.7), and alkalinization, and sulfur fugacity remained stable within a narrow range (log fS₂ = −13.6 to −8.0), followed in Stage 4 by minor reheating to ~280 °C, re-acidification, and a slight rebound in oxygen fugacity. Thermodynamic simulations reveal that the destabilization of Au(HS)₂⁻ complexes, primarily driven by the synergistic effects of cooling, pH increase, and decreasing oxygen fugacity, triggered gold precipitation during the main ore stage. Results demonstrate that abrupt cooling coupled with fluid alkalinization and reduction exerted the dominant control on gold precipitation in Jinshan, resolving long-standing debates on ore-forming mechanisms and highlighting chlorite as a robust quantitative sensor for fluid evolution. Full article

The North China Craton (NCC) hosts numerous world-class Au deposits and these Au deposits can be classified into the Au-only and Ag-Au polymetallics, respectively. The former is mostly located in the eastern NCC, such as in the giant Jiaodong Province, and the latter is mostly distributed along the northern and southern margins of the NCC. Compared with Au-only deposits, the ore genesis of the Ag-Au deposits remains controversial. This paper focuses on the Niujuan Ag-Au deposit in the Fengning ore cluster of the northern margin of the NCC. Detailed deposit geology investigation, texture analysis, and analyses of the in situ trace element and sulfur isotope compositions of pyrite, coupled with H-O isotope compositions of quartz from different stages, were conducted to elucidate the ore-forming processes and metal sources. The results showed that the formation of the Niujuan deposit can be divided into four stages, including a pre-ore siliceous breccia stage (stage 1), syn-ore quartz-pyrite stage (stage 2), syn-ore polymetallic sulfide stage (stage 3), and post-ore fluorite-calcite stage (stage 4). Among these, stage 3 represents the major Ag-Au mineralization stage. Pyrite is well developed within stage 2 and stage 3, representing the intensive sulfidation of the wall rock. Microscopic analytical techniques including gamma-enhanced reflected light and scanning electron microscopy backscattered electron (BSE) reveal that pyrite samples from stage 2 and stage 3 have distinct textures. Pyrite (Py1) from stage 2 is homogeneous but with numerous pores. In contrast, pyrite (Py2) from stage 3 has overgrowth textures, and be divided into three sub-stages from core to rim (Py2a, Py2b, and Py2c) with different BSE brightness levels. LA-ICP-MS trace elements analyses results show that these different stages of pyrite show different composition such as Au, As, Ag, Co, and Ni. Py1 has low Au and Ag concentrations ranging from <0.1 ppm to 0.02 ppm and <0.1 ppm to 21.8 ppm, respectively. Py2a has low Au and Ag concentrations ranging from <0.1 ppm to 0.4 ppm and 0.4 ppm to 118.4 ppm, respectively. Py2b is characterized by high As and low Au contents, with average values of 6670.8 ppm for As and 1.4 ppm for Au. Py2c shows relatively low Co and Ni concentrations ranging from 0.02 ppm to 255.2 ppm and <0.1 ppm to 9.9 ppm, respectively. The sulfur isotope composition of Py1 and Py2 is relatively consistent, ranging from 3.8‰ to 6.7‰. The H and O isotope compositions of quartz from stage 1, stage 2, and stage 3 have insignificant variations, ranging from −119.5‰ to −101.3‰ for δD and −6.8‰ to −3.7‰ for δ¹⁸O_fluid, respectively. The results show that sulfur and, possibly, Au and Ag were mainly derived from magmatic hydrothermal fluids, and a significant amount of meteoric water was involved. Combined with the published mineralizing ages (~140 Ma), this paper suggests that the Niujuan Ag-Au deposit formed during the Early Cretaceous under an extensional setting in response to the eastward retreating subduction of the Paleo-Pacific oceanic plate. Evidence from deposit geology and geochemistry reveals that the mixture of magmatic and meteoric water, together with intensive sulfidation, is the key factor controlling Au and Ag deposition. Full article

The Bagenheigqier medium-sized Pb-Zn deposit is located in central-southern segment of Great Xing’an Range, northeastern China, where its vein-type orebodies are hosted within the structural contact zone between the Lower Permian Dashi Formation and granite porphyry intrusions. Five mineralization stages are divided into skarn (I), oxide (II), quartz-pyrite-arsenopyrite (III), quartz-polymetallic sulfide (IV), and quartz-calcite-pyrite (V). Three types of fluid inclusions (FIs) are identified in Bagenheigeqier Pb-Zn deposit, including daughter mineral-bearing three-phase (SL-type), vapor–liquid two-phase (VL-type), and vapor-rich two-phase (LV-type) FIs. All FI types occur in Stages I–III, with homogenization temperatures (Th) of 423–486, 389–441, 362–408 °C, and salinities of 1.1–49.2, 0.9–43.9 and 0.9–38.8 wt.% NaCl equiv, respectively. Stage IV hosts only VL- and LV-type FIs (Th: 277–319 °C; salinity: 2.1–8.7 wt.% NaCl equiv), whereas Stage V contains exclusively VL-type FIs with Th of 173–214 °C and salinity of 1.2–5.7 wt.% NaCl equiv. The H-O isotopic results of quartz in stage II–IV (δD = −103.5‰–−99.1‰, −115.7‰–−107.8‰ and −121.5‰–−117.2‰; δ¹⁸O_H2O = 4.4‰–7.1‰, 1.1‰–3.5‰ and −4.6‰–−3.5‰) indicate the ore-forming fluids are predominantly of magmatic origin with subordinate meteoric water mixing. Fluid boiling and the mixing of meteoric water may lead to the precipitation of metal. The in situ trace elements analyses indicate that sphalerites in main mineralization stage are enriched in Fe, Mn, Co and In and depleted in Ga and Ge. The calculation results suggest that the sphalerites crystallized under moderate temperature conditions (286–330 °C) and intermediate f_S2 (−10.5 to −9.2) conditions. The geological, fluid inclusion, isotopic and trace element evidences indicate that the Bagenheigeqier deposit is classified as a skarn-type deposit. Full article

This study investigates the genesis of gold mineralization at the Rodruin prospect in the central Eastern Desert (CED) of Egypt, with the aim of constraining the relative contributions of metamorphic and magmatic fluids to ore formation. Gold mineralization at Rodruin is hosted by quartz–carbonate veins emplaced within a shear zone that transects low-grade metasedimentary sequences intruded by Ediacaran post-tectonic granitoids. It exhibits characteristics transitional between orogenic turbidite-hosted and polymetallic vein-type mineralization. Although metamorphic devolatilization is interpreted to have generated the dominant ore-forming fluids, adjacent granitoid intrusions acted primarily as a thermal engine, with only a limited direct input of magmatic-hydrothermal fluids. This interpretation is supported by the occurrence of magmatic-affiliated mineral inclusions (monazite, cassiterite, and zircon) coupled with generally low concentrations of trace elements typically enriched in granitic magmatic-hydrothermal fluids (Sb, Bi, Mo, W, Sn, Nb, and Ta), collectively indicating a subordinate magmatic contribution. Rare earth element (REE) patterns of the ore samples closely resemble those of the nearby granitoids, displaying LREE enrichment; however, a distinct positive Eu anomaly is restricted to the ore assemblages and is attributed to hydrothermal feldspar alteration supporting magmatic involvement in ore formation. Carbon and oxygen isotope compositions (δ¹³C = −6.6 to −2.36‰; δ¹⁸O = +15.7 to +19.7‰), together with REE signatures comparable to primitive mantle values and textural evidence for synchronous sulfide–carbonate precipitation, manifested by rhythmic banding of carbonates and sulfides unequivocally indicate a hydrothermal–metasomatic origin. Collectively, these lines of evidence support a hybrid metamorphic–magmatic model in which gold and associated base metals were predominantly transported by metamorphic fluids, whose mobilization and focusing were enhanced by the thermal influence of Younger granitic intrusions, whereas magmatic-hydrothermal fluids contributed only a minor proportion to the overall metal budget. Full article