Hydrothermal Alteration Processes of Xincheng Gold Deposit Jiaodong Peninsula, China: Constraints from Composition of Hydrothermal Rutile

Delineating the process of hydrothermal alteration is crucial for effectively enhancing exploration strategies and better understanding the gold mineralization process. Rutile, with its capacity to accommodate a wide range of trace elements including high-field-strength elements and base metals, serves as a reliable fluid tracer in ore systems. As one of the most significant gold ore concentrations globally, Jiaodong boasts a gold reserve exceeding 5500 t. The Xincheng gold deposit is a world-class high-grade mine, boasting a proven gold reserve exceeding 200 t, and stands as one of the largest altered-type gold deposits in the vast gold province of the Jiaodong Peninsula, Eastern China. In this study, rutile (Rt1,2,3) was identified in the K-feldspar alteration, sericitization, and pyrite–sericite–quartz alteration stages of the Xincheng gold deposit in Jiaodong based on petrographic characteristics. Rt1 coexists with hydrothermal K-feldspar and quartz, while Rt2 coexists with minerals such as sericite, quartz, muscovite, and pyrite. Rt3 is widely distributed in hydrothermal veins and is primarily associated with minerals including quartz, pyrite, chalcopyrite, and sericite. Raman spectroscopy, EPMA, and LA-ICP-MS analysis were conducted to investigate the characteristics and evolution of altered hydrothermal fluids. This study indicates that the Zr vs. W and Nb/V vs. W diagrams suggest that Rt1 is of magmatic–hydrothermal origin, while Rt2 and Rt3 are of metamorphic–hydrothermal origin. Notably, the W content in Rt2 and Rt3 is significantly higher than in Rt1 (<100 ppm), suggesting a close relationship between the W content in rutile and mineralization. The three types of rutile exhibit significantly different concentrations of trace elements such as W, V, Nb, Zr, Sn, and Fe, displaying distinct bright spots and elemental zoning characteristics in backscattered electron images and surface scans. These features arise from the isomorphic substitution of Ti4+. While Rt1 exhibits no significant element exchange with the hydrothermal fluids, Rt2 and Rt3 show a stronger substitution of W, Nb, V, and Fe, indicating a gradual enrichment of F and Cl in the fluids. This process activates and transports these elements into the fluids, leading to their continuous accumulation within the system. From Rt1 to Rt3, the increasing concentrations of Fe and W, along with the negative Eu anomaly, suggest a decrease in fluid temperature and oxygen fugacity during the alteration and mineralization process. The gradual increase in the contents of REEs and high-field-strength elements such as W, V, Nb, and Sn indicates that the hydrothermal fluids are enriched in F and Cl, exhibiting weak acidity. The nature of the fluids during hydrothermal alteration is closely related to the composition of rutile, making it a promising tool for studying hydrothermal alteration and related mineralization processes.