4.6 Article

Biotite composition as a tracer of fluid evolution and mineralization center: a case study at the Qulong porphyry Cu-Mo deposit, Tibet

Journal

MINERALIUM DEPOSITA
Volume 57, Issue 6, Pages 1047-1069

Publisher

SPRINGER
DOI: 10.1007/s00126-021-01085-w

Keywords

Biotite; Chemical composition; Fluid evolution; Porphyry Cu-Mo deposit; Qulong deposit

Funding

  1. National Natural Science Foundation of China [41972089, 41872086, 41972083]
  2. National Key R&D Program of China [2016YFC0600308]

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This study investigates the composition and evolution of magmatic-hydrothermal fluids in the Qulong porphyry Cu-Mo deposit in Tibet. It reveals that the increase in Fe, Ti, Co, Zn, and Cl and decrease in Mg, Ge, and F contents in hydrothermal biotite near the core of the deposit may be an important indicator of high-grade mineralized zones. Furthermore, the systematic spatial variations in hydrothermal biotite chemistry can potentially be utilized as a prospecting tool for porphyry deposits worldwide.
Porphyry Cu-Mo deposits are magmatic-hydrothermal deposits in which sulfide and oxide minerals precipitate from aqueous solutions. However, many questions remain about the composition and evolution of the magmatic-hydrothermal fluids responsible for mineralization. In response to this knowledge gap at the Qulong porphyry Cu-Mo deposit, Tibet, we present a comprehensive major and trace element dataset for biotite (including halogens) from Qulong to elucidate magmatic-hydrothermal fluid compositions and fluid evolution. Based on genesis and occurrence, biotite is divided into primary (igneous), re-equilibrated (igneous modified by hydrothermal fluids), and secondary (hydrothermal) types. All studied biotite grains are Mg-rich, and X-Mg values (0.59-0.90) increased during fluid evolution, perhaps controlled by high oxygen fugacity (fO(2)) and sulfur fugacity (fS(2)) in the magmatic-hydrothermal fluids. The IV(F) and IV(Cl) values and halogen fugacity of biotite indicate that Cl-rich fluids were dominant during early magmatic-hydrothermal evolution, while later fluids were enriched in F. This is consistent with early Cu and late Mo enrichment in the Qulong deposit. We propose a fluid evolution model based on in situ major and trace element data and cross-cutting relationships between the intrusions and the veins. Iron, Ti, Co, Ni, Zn, and Cl contents decreased, while Mg, Si, Al, Sn, Ge, and F contents increased during the evolution of the magmatic-hydrothermal fluid. Importantly, the increase in Fe, Ti, Co, Zn, and Cl and decrease in Mg, Ge, and F contents in hydrothermal biotite as the core of the deposit is approached (extending to similar to 2.5 km depth) may prove to be an important indicator of high-grade mineralized zones. Finally, this study shows that systematic spatial variations in hydrothermal biotite chemistry can potentially be used as a prospecting tool for porphyry deposits worldwide.

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