Startseite Hydrothermal fluid signatures of the Yulong porphyry Cu-Mo deposit: Clues from the composition and U-Pb dating of W-bearing rutile
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Hydrothermal fluid signatures of the Yulong porphyry Cu-Mo deposit: Clues from the composition and U-Pb dating of W-bearing rutile

  • Qi Chen , Changming Wang , Leon Bagas , Bin Du , Kangxing Shi und Jiaxuan Zhu
Veröffentlicht/Copyright: 31. Mai 2023
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Abstract

Hydrothermal rutile (TiO2) is a widely distributed accessory mineral in hydrothermal veins or alteration assemblages of porphyry deposits and provides important information for further understanding hydrothermal fluid signatures. This study determines the geochemical composition and U-Pb dates of hydrothermal rutile from the Yulong porphyry Cu-Mo deposit in east Tibet, China. Three types of TiO2 polymorphs have been identified based on their Raman spectroscopic, textural, and chemical characteristics. (1) Brookite and anatase pseudomorphs after titanite in a fine-grained matrix, indicating low-temperature hydrothermal fluids destabilizing primary Ti-bearing minerals during argillic alteration (type-I). (2) Elongated and prismatic rutile present in hydrothermal veins or in clusters in accompanying alteration envelope characterized by weak zoning (type-II). And (3) rutile intergrown with sulfides in hydrothermal veins, characterized by well-developed patchy and sector zoning (type-III). In contrast to the type-I and type-II TiO2 polymorphs, tungsten is enriched in backscattered bright patches and sector zones in type-III rutile, which is due to the substitution of W6+ in the Ti4+ octahedral site. The mechanism of the enrichment of tungsten is efectively driven by the halogen-rich (F, Cl) aqueous fluids during hydrothermal mineralization. In situ U-Pb dating of the type-III rutile yields a lower intercept age of 41.8 ± 1.2 Ma, which brackets the timing of the Cu-Mo mineralization. The relationship between rutile textures and composition indicates that W-bearing rutile can serve as a recorder of hydrothermal processes in porphyry Cu deposits.

Funding statement: This work was supported by the National Key Research and Development Project of China (Number 2020YFA0714802), the National Natural Science Foundation of China (Numbers 41872080), and the Most Special Fund from the State Key Laboratory of Geological Processes and Mineral Resources in China University of Geosciences (Beijing) of China (Number MSFGPMR201804).

Acknowledgments

We thank Diana Zivak, University of Adelaide, Australia, and the anonymous journal reviewers for their critical reviews and constructive comments. We are also grateful to Associate Editor Paul Tomascak for their valuable help in handling this paper. We are grateful to Shentai Liu, the Engineer of Tibet Yulong Copper Co. Ltd., for his assistance during the field investigation.

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Received: 2022-01-16
Accepted: 2022-07-09
Published Online: 2023-05-31
Published in Print: 2023-06-27

© 2023 by Mineralogical Society of America

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