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[Display omitted] • Five ore-forming stages are recognized in the Yechangping porphyry-type orebodies. • Fluid characteristics suggest that Yechangping is a Dabie-type porphyry Mo deposit. • The process of fluid immiscibility, boiling, and mixing cause the mineralization. • Magmatic-hydrothermal system of Yechangping deposit extends to depths of 10 km. Dabie-type porphyry Mo deposits have recently emerged as a distinct subtype of porphyry Mo deposits, but questions remain about the magmatic-hydrothermal fluid evolution in the formation of this type of deposit. Here, well-developed fluid inclusions in quartz phenocrysts, unidirectional solidification textures (UST), and quartz veins in the Yechangping porphyry Mo-W deposit, Qinling Orogen, completely record the magmatic-hydrothermal mineralization process. The characteristics and evolution of the ore-forming fluid in this deposit are investigated through petrography, microthermometry, and laser Raman spectroscopy analysis of fluid inclusions at different stages in order to improve our understanding of the fluid evolution in the genesis of Dabie-type porphyry Mo deposit. The mineralization process in the porphyry-type orebody can be divided into three periods and five stages: (1) magmatic period, including quartz phenocrysts (stage 1); (2) magmatic-hydrothermal transition period, including UST (stage 2); (3) hydrothermal period, including quartz ± K-feldspar veins (stage 3), quartz-molybdenite veins (stage 4), and calcite ± quartz veins (stage 5), where stage 4 is the main ore-forming stage. The fluid inclusions in quartz and calcite can be recognized as pure CO 2 (PC type), CO 2 -H 2 O (C type), daughter minerals-bearing (S type), and H 2 O (WV type and WL type) inclusions. Ore-forming fluid is initially high temperature, high salinity, and CO 2 -rich, belonging to the H 2 O-CO 2 -NaCl (±KCl) system suggested by the fluid inclusions identified in UST. The estimated lithostatic pressures of stage 1 range from 284–362 MPa, corresponding to depths of 10.3 to 13.2 km, which are consistent with the formation depth of the underlying magma chamber. The presence of UST in stage 2 indicates that the magma was saturated with fluid. Due to the fluctuating pressure (123–260 MPa) in UST of stage 2, fluid immiscibility happened soon after the fluid exsolution and is inferred to occur between the CO 2 -rich and aqueous phases. Then, the fluid boiling and mixing occurred in stages 3 and 4, respectively. The estimated pressures of stage 4, which represent the main mineralization stage, range from 45–175 MPa, corresponding to depths of 4.6–6.4 km. The immiscibility of CO 2, along with the fluid mixing-induced cooling and dilution, caused an increase in p H and a decrease in oxygen fugacity, which serves as a crucial mechanism for Mo mineralization at the Yechangping deposit. Stage 5 is characterized by low temperature (185–309 °C) and low salinity (2.9–8.7 wt% NaCl equiv.). The primary high temperature, high salinity, CO 2 -rich fluids, and relatively deep ore-forming depth suggest that the Yechangping deposit is a typical example of a Dabie-type porphyry deposit. The characteristics of fluids and the variation in estimated depth at each stage record the evolutionary process of a magmatic-hydrothermal system extending to depths of nearly 10 km in the Yechangping deposit. [ABSTRACT FROM AUTHOR]

[Display omitted] • Zircon U-Pb ages record two phases of granitic magmatism of 159 and 145 Ma. • Molybdenum and W are enriched in porphyry by prolonged fractionation and high f O2. • Scheelite petrography and compositions reflect mechanisms of Mo-W mineralization. • Porphyry-skarn Mo-W systems may be controlled by magmatic sources and wall rocks. Eastern Qinling Orogen is the largest Mo province in the world, hosting nine giant Mo deposits. Four giant Mo deposits contain economic W mineralization, while the mechanism of W mineralization remains unclear. The Yechangping deposit is a representative porphyry-skarn Mo-W deposit, with four paragenetic stages of prograde skarn, retrograde skarn, polymetallic sulfides and carbonate stage. Magmatism at Yechangping includes early barren monzogranite porphyry at 159.0 ± 1.5 Ma and late ore-related granite porphyry at ca. 145 Ma, and the latter porphyry shows a higher magmatic fractionation than the early barren monzogranite porphyry. Both barren and ore-related porphyries have similar high magma oxidation states, which may efficiently extract Mo during partial melting and hinder subsequent molybdenite crystallization until the porphyry-skarn Mo mineralization. Three types of scheelites are distinguished by their texture, paragenetic relationship and geochemistry, including Sch-1a in the retrograde skarn stage, and Sch-1b and Sch-2 in the polymetallic sulfides stage. Scheelite displays decreasing MoO 3 contents from 7.01–51.59 % in Sch-1a, through 3.15–17.51 % in Sch-1b, to 0–1.51 % in Sch-2. The decreasing MoO 3 contents in scheelite are attributed to the transformation of dominant Mo-bearing phases, i.e., from retrograde skarn stage powellite to polymetallic sulfides stage molybdenite. We suggest that the Mo-W mineralization is triggered by the decreasing oxygen fugacity, p H, and temperature, supported by thermodynamic modeling. In addition, the precipitation of fluorite and destabilization of fluorine complexes may have also promoted the Mo-W mineralization. Zircon Hf isotopes yielded ε Hf (t) values of −14.9 to −7.5 and T DM2 ages of 1671–2147 Ma, indicating that Yechangping porphyries were primarily sourced from the ancient basement of the Huaxiong Block, with additional contribution from the North Qinling Accretionary Belt. Skarn W mineralization in the southern part of Huaxiong Block may be controlled by both magmatic fertility and carbonate wall-rocks. [ABSTRACT FROM AUTHOR]