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The Bangongco–Nujiang metallogenic belt of Tibet is a main suture zone in the Qinghai–Tibet Plateau, which is known as an important porphyry–epithermal–skarn Cu-polymetallic mineralization zone in China. The western part of the Bangongco–Nujiang metallogenic belt exposes several medium high-silica terrestrial alkaline volcanic rocks with strong alteration influenced by collision orogeny. Some research has shown that clues to mineralization such as malachite and gossan are found on the surface. However, volcanic rock areas with varied topography place a huge burden on geological investigation, and the existing research on predicting mineralization is relatively scarce. This paper describes the extraction of alteration mineral information based on medium spatial resolution and hyperspectral resolution images, establishing a spectral library of alteration minerals in this area. By analyzing radar data, digital elevation, and synthesis results of different spectral bands, we combine remote sensing with geographic information technology to establish crater markers. The extraction results from multisource and chemical exploration data are superimposed onto the analysis of mineralization characteristics and geological conditions so as to establish the mineralization signatures for terrestrial volcanic rock areas. Eighteen mineralization prospect areas were identified, which can provide technical support for future mineralization research in this belt. [ABSTRACT FROM AUTHOR]

The Bangpu porphyry Mo–Cu deposit is a representative Mo-dominated deposit besides the Sharang porphyry Mo deposit in the Gangdese metallogenic belt. The Mo–Cu mineralization has a close relationship with the monzogranite porphyry and diorite porphyrite. We identify three stages during the ore formation: a pre-ore stage, a main-ore stage with Mo–Cu deposited dominantly, and a post-ore stage. In this study, He–Ar, H–O, S and Pb isotopic compositions of the Bangpu deposit were determined. Based on these determinations, integrated isotope geochemistry studies were performed to constrain the possible sources of the ore-forming fluids and metals. The 3 He/ 4 He and 40 Ar/ 36 Ar ratios of fluid inclusions exhibit a range of 0.12209–0.36370 Ra and 275.6–346.1, respectively. The 4 He and 40 Ar concentrations vary from 1.51 to 3.57 (10 −7 cm 3 STP g −1 ) and 0.49 to 9.31 (10 −7 cm 3 STP g −1 ), respectively. He–Ar isotopic compositions suggest dominantly crustal-derived fluid with minor amount of meteoric water in the main ore stage. The δ 18 O fluid and δD fluid values vary from −1.3‰ to 3.9‰ and −140.5‰ to −73.7‰, respectively, indicating that magma fluids mixed with meteoric water. The average δ 34 S value of the sulfides (0.3‰) in the main-ore stage is close to the ore-forming porphyries, indicating a magmatic source. The lead isotopic components of ore sulfides exhibit restricted ranges with 206 Pb/ 204 Pb, 207 Pb/ 204 Pb, and 208 Pb/ 204 Pb ratios of 18.450–18.728, 15.602–5.672, and 38.715–39.211, respectively and μ values in the range of and 9.46–9.58, indicating ore-forming metals of primarily an upper crust source with a small amount of mantle materials. Compared to the Bangpu deposit, the ore metals derived from mantle are even greater in the Jiama and Qulong deposits, which leads to Cu being the dominant mineralization in the Jiama and Qulong deposit. [ABSTRACT FROM AUTHOR]

The coexistence of aqueous fluid inclusions and silicate melt inclusions in quartz phenocrysts from porphyrites at the Bangpu porphyry Mo–Cu deposit, Tibet, China were examined to characterize the immiscibility processes during the magmatic to hydrothermal transition. The physical and chemical environment during crystallization of the magmas has been reconstructed on the basis of microthermometric experiments and trace element microanalysis. Compositions of melt and brine fluid phases are determined using Synchrotron radiation X-ray fluorescence analysis, SEM–EDS and Laser Raman spectroscopy analyses. Brine fluids were directly exsolved by a crystallizing melt, and the simultaneous entrapment of volatile-rich (brine fluid) and volatile-poor immiscible phases (silicate melt) occurred at 670–700 °C and 1.6–1.95 kbar when the magma had H 2 O contents between 5 and 6 wt% and crystal contents of 60–80%. A later low-density fluid with a higher Mo concentration exsolved after about 80–90% crystallization had occurred. This fluid contained significant concentrations of Cl, Na, K, Ca, Fe, Cu, Zn, Rb, and small amounts of Mn, Br and Pb. Immiscibility of magmatic fluids can lead to different metal partitioning behaviors between residual melt and volatile phases, which generate variable metal ratios. Copper was partitioned preferentially into the brine phase, in contrast to the behavior observed in other porphyry Cu deposits. Ore deposition by a dense brine could explain the partially deep Cu mineralization. Condensation of brine from a later low-density parental fluid could be an efficient mechanism to concentrate shallow Cu mineralization and broadly distributed Mo mineralization. The source of the Mo mineralizing fluids probably was a particularly large magma chamber that crystallized and fractionated at depth greater than upper continental crust level. [ABSTRACT FROM AUTHOR]