The Gayahedonggou magmatic Cu-Ni sulfide deposit was recently discovered in the East Kunlun orogenic belt (Northern Tibetan Plateau, China). The mineralization in this region is associated with mafic–ultramafic intrusions. To date, the formation age and metallogenic model of these ore-bearing intrusions have not been studied systematically. In this paper, the petrology, zircon U-Pb chronology, and geochemistry of ore-bearing wehrlite and quartz diorite are investigated. The results show that the zircon U-Pb isotopic age of wehrlite is 419.9 ± 1.5 Ma with an average εHf(t) value of 3.0, indicating that wehrlite originated from a depleted mantle or the asthenosphere. The (La/Yb)_N, (La/Sm)_N, (Gd/Yb)_N, Nb/U, and Ce/Pb ratios of wehrlite are between 3.01–7.14, 1.69–3.91, 1.36–1.51, 2.07–2.93, and 0.55–1.42, respectively, indicating that the parent magma of the wehrlite had been contaminated by the upper crust. The zircon U-Pb isotopic age of quartz diorite is 410.2 ± 3.5 Ma with an average εHf(t) value of 8.0, and the A/CNK and A/NK ratio of quartz diorites ranges from 1.02 to 1.04 and from 2.13 to 2.23, respectively. These features are similar to those of the type I granite, and the quartz diorite was likely derived from the lower crust. Combined with the regional geological evolution, the Gayahedonggou complex formed in a post-collision extensional environment. The pyroxene in the Gayahedonggou complex is mainly clinopyroxene, which is enriched in the CaO content, indicating that the CaO content of the parent magma of the Gayahedonggou complex is high or that the complex has been contaminated by Ca-rich surrounding rocks, which hinders Cu-Ni mineralization.

The East Kunlun Orogenic Belt is considered as one of the important gold mineralization regions in the Tethys tectonic domain. These orogenic gold deposits are related to intermediate-acid intrusions formed at the end of Paleo-Tethys evolution, but the petrogenesis is controversial. This paper presents a new study on the geochemistry of zircon U-Pb, O, S, and Pb isotopic compositions of Asiha quartz diorite, granite porphyry, and sulfides. The geochemical features of quartz diorite and granite porphyry are consistent with the modern adakite, with high content of Sr but low content of Y, Yb, and MgO. Magmatic zircons from these two types of intrusion yielded U-Pb ages of 238.4 ± 1.4 Ma and 240 ± 1.7 Ma, respectively. The high O isotopic composition of Asiha complex may reflect that crust or crustal derivates were incorporated into the magmatic melt, and the Pb isotope characteristics indicates a lower crust origin. The δ³⁴S values of pyrites range from 4.9‰ to 11.6‰. This study infers that the Asiha complex perhaps formed by partial melting of the Paleo-Tethys subducted oceanic crust with seafloor sediments and is markedly different from the traditional adakite. Asiha deposit is an orogenic gold deposit related to adakite-like rocks, which formed in Triassic in the East Kunlun Orogenic Belt.

The Reshui porphyry Mo deposit is located in the East Kunlun orogenic belt (EKOB). Molybdenum mineralization is distributed in monzogranite and porphyritic monzogranite rocks, mainly presenting as various types of hydrothermal veinlets in altered wall rocks, and the orebodies are controlled by three groups of fractures. In this paper, we present the results of fluid-inclusion and isotopic (S and Pb) investigations of the Reshui Mo deposit. The ore-forming process of the deposit can be divided into three stages: an early disseminated molybdenite stage (stage 1), a middle quartz–molybdenite stage (stage 2) and a late quartz–polymetallic sulfide stage (stage 3). The alteration was mainly potassic and silicic in stage 1, silicic in stage 2, and sericitic and silicic in stage 3. Five types of fluid inclusions (FIs) can be distinguished in quartz phenocrysts and quartz veins, namely W, PL (pure liquid inclusions), PV (pure gas inclusions), C (CO₂ three-phase inclusions), and S (daughter mineral-bearing inclusions). The homogenization temperatures of fluid inclusions belonging to stages 1 to 3 are 282.3–378 °C, 238.7–312.6 °C and 198.3–228 °C, respectively. The fluid salinities at stages 1 to 3 are 4.65–8.14% NaCl eq., 4.34–42.64% NaCl eq., and 3.55–4.65% NaCl eq., respectively. The fluids of this deposit were generally moderate–high temperature and moderate–low salinity and belong to the H₂O–NaCl–CO₂ ± CH₄ system. The temperature and pressure changed considerably between stage 2 (high–medium-temperature) and stage 3 (low-temperature). The evidence for ore-forming fluids containing different types of coexisting inclusions in stage 2 and a decrease in the fluid temperature from stage 2 to stage 3 indicate that fluid boiling and fluid mixing were the main mechanisms of ore precipitation. The sulfide ³⁴S_V-CDT values range from 4.90‰ to 5.80‰, which is characteristic of magmatic sulfur. The ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb, and ²⁰⁸Pb/²⁰⁴Pb values of the ore minerals are 18.210–18.786, 15.589–15.723, and 38.298–39.126, respectively. These lead isotopic compositions suggest that the ores were mainly sourced from crustally derived magmas, with minor input from the mantle. The fluid inclusions and S–Pb isotopes provide important information on the genesis of the Reshui porphyry Mo deposit and indicate that the Triassic has high metallogenic porphyry potential in the EKOB.