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The Sinongduo mining region includes two types of mineralizations: the epithermal and the carbonate‐hosted Pb‐Zn‐Ag deposits. Despite being studied for many years, the ore formation process and genesis of the carbonate‐hosted Pb‐Zn‐Ag deposits remain poorly understood. The Pb‐Zn‐Ag ore bodies occur as veins and are hosted by limestone and dolostone of the Permian Xiala Formation. Three sulfide mineralization substages have been identified at the Sinongduo carbonate‐hosted deposit. Indium coupled with Cu, Co and Sn was incorporated into sphalerite as substitutions: 2Zn2+ ↔ Cu+ + In3+, (3n/2 + 1)Zn2+ ↔ Co2+ + nIn3+ or (2n + 1)Zn2+ ↔ Co2+ + n(Cu+ + In3+) (n > 1) and 4Zn2+ ↔ Sn2+ + 2In3+. Sphalerite and pyrite in the mineralization stage display δ34S values in a narrow range of +5.7‰ to +11.3‰, which are similar to those of Palaeocene igneous rocks, indicative of a magmatic source of sulfur. We present systematic carbon‐hydrogen‐oxygen isotope results that further support a magmatic source for the ore‐forming fluids that were influenced by meteoric water. Furthermore, the Pb isotope compositions of sulfide minerals in the Sinongduo carbonate‐hosted deposit overlap with the values of coeval Linzizong volcanic rocks and are similar to those of Indian Ocean sediments, indicating upper crustal sources of metals. We conclude that the Sinongduo carbonate‐hosted Pb‐Zn‐Ag deposit is a medium‐ to low‐temperature magmatic‐hydrothermal deposit related to Linzizong magmatism. [ABSTRACT FROM AUTHOR]

The Jiama deposit, a significant porphyry‐skarn‐type copper polymetallic deposit located within the Gangdese metallogenic belt in Tibet, China, exemplifies a typical porphyry metallogenic system. However, the mineral chemistry of its accessory minerals remains under‐examined, posing challenges for resource assessment and ore prospecting. Utilizing electron microprobe analysis and LA‐ICP‐MS analysis, this study investigated the geochemical characteristics of apatite in ore‐bearing granite and monzogranite porphyries, as well as granodiorite, quartz diorite, and dark diorite porphyries in the deposit. It also delved into the diagenetic and metallogenic information from these geochemical signatures. Key findings include: (1) The SiO2 content, rare earth element (REE) contents, and REE partition coefficients of apatite indicate that the dark diorite porphyry possibly does not share a cogenetic magma source with the other four types of porphyries; (2) the volatile F and Cl contents in apatite, along with their ratio, indicate the Jiama deposit, formed in a collisional setting, demonstrates lower Cl/F ratios in apatite than the same type of deposits formed in a subduction environment; (3) compared to non‐ore‐bearing rock bodies in other deposits formed in a collisional setting, apatite in the Jiama deposit exhibits lower Ce and Ga contents. This might indicate that rock bodies in the Jiama deposit have higher oxygen fugacity. Nevertheless, the marginal variation in oxygen fugacity between ore‐bearing and non‐ore‐bearing rock bodies within the deposit suggests oxygen fugacity may not serve as the decisive factor in the ore‐hosting potential of rock bodies in the Jiama deposit. [ABSTRACT FROM AUTHOR]

• CH 4 was generated by the thermal decomposition of the carbonaceous wall-rocks. • CH 4 added, which contributed to the system from oxidized to reduced conditions. • Ore elements were deposited via fluid boiling process. High f O 2 conditions characterize the majority of global porphyry copper deposits and contain highly oxidized minerals, such as magnetite and anhydrite. In contrast, the No. 1 porphyry Cu–Au deposit in the Xiongcun district (Tibet, China) has abundant pyrrhotite, reduced fluids (CH 4 ≫ CO 2), and a relative lack of highly oxidized minerals, which are indicative of low f O 2 conditions. Scanning electron microscopy, fluid inclusion, C–H–O–He–Ar isotopes, and whole-rock organic carbon contents and isotope analysis were used to constrain the evolution of ore-forming fluid, the origin of CH 4 and metal deposition mechanisms for the No. 1 deposit. The He–Ar isotopic compositions (3He/4He = 0.11–0.96 Ra, 40Ar/36Ar = 418.7–2920.2) suggest that the ore-forming fluids predominantly derived from crust source with minor mantle input. The H–O isotopic analysis results (δ18O H2O = −1.8 to +5.2‰, δD = −106 to −89.9‰) indicate that the ore-forming fluids were derived from a magmatic source that mixed with some meteoric waters. The element compositions of zircons and fluid/melt inclusions from the mineralized Middle Jurassic quartz diorite porphyry reveal that the primary magma was characterized by high log f O 2 (>NNO) conditions. The quartz diorite porphyry intruded into the carbon-bearing wall rocks produced abundant CH 4 by thermal decomposition of organic matter (δ13C CH4 = −26.3 to −28.5‰), which changed the redox state of the porphyry copper system from oxidized to reduced condition. Ore elements were deposited via fluid boiling as a consequence of the rapid decrease in temperature and pressure. [ABSTRACT FROM AUTHOR]