No abstract

The Qulong deposit in Tibet is one of the largest porphyry copper-molybdenum deposits in China. We used short -wave infrared (SWIR) spectroscopy to examine the spectral characteristics of the extensively developed chlorite in this deposit. X-ray diffraction and electron microprobe analyses were used for phase identification and to obtain the chemical composition, ion substitution relationships, and formation environment of the chlorite. SWIR spectral parameters were applied to detect the hydrothermal centers. The results indicate that the wavelength of the absorption feature for Qulong chlorite Fe-OH (Pos2250) range from 2240 to 2268.4 nm; the chlorite substitution relationships are dominated by Mg-Fe substitution at the octahedral sites together with Al Ⅳ -Si substitution at the tetrahedral sites; the chlorite formation temperatures range within the medium-low temperature hydrothermal alteration range from 164 to 281°C, with an average value of 264°C; the wavelength of the chlorite peak position for Fe-OH (2250 nm) absorption and its chemical composition are positively correlated with Al Ⅵ , Fe + Al Ⅵ , Fe/(Fe + Mg), Fe, and Fe + Al Ⅳ but negatively correlated with Mg and Mg/ (Fe + Mg); and the wavelength associated with the chlorite Fe-OH (2250 nm) absorption feature is positively correlated with the temperature at which the chlorite formed. These correlations indicate that more Fe and Al Ⅵ ions and fewer Mg ions at the octahedral sites of chlorite lead to a longer the wavelength of the chlorite Fe-OH (2250 nm) absorption feature and a higher chlorite formation temperature. The wavelength of the Qulong chlorite Fe-OH (2250 nm) absorption feature (>2252 nm) can thus serve as an exploration indicator to guide the detection of hydrothermal centers in porphyry copper deposits. The results of the study indicate that the mineralogical and SWIR spectral characteristics of chlorite are significant indicators for locating hydrothermal centers within porphyry deposits.

Continental crust has long been considered too buoyant to be subducted beneath another continent, although geophysical evidence in collision zones predict continental crust subduction. This is particularly significant where upper continental crust is detached allowing the lower continental crust to subduct, albeit the mechanism of such subduction and recycling of the upper continental crust remain poorly understood. Here, we investigate Paleocene S-type magmatic and volcanic rocks from the Linzizong volcanic succession in the southern Lhasa block of Tibet. These rocks exhibit highly enriched 87Sr/86Sr, 207Pb/206Pb and 208Pb/206Pb together with depleted 143Nd/144Nd isotope ratios. The geochemical and isotopic features of these rocks are consistent with those of modern upper continental crust. We conclude that these Paleocene S-type volcanic and magmatic rocks originated from the melting of the upper continental crust from microcontinent subduction during the late stage of India–Asia convergence.

Field measurements of the thermal infrared (TIR) reflectance from drill hole samples proved to be an effective method to map variations in garnet species associated with hydrothermal alteration zonation of the Jiama porphyry-skarn Cu deposit 1# skarn orebody, Tibetan Plateau, China. The TIR mineral spectral information was combined with electron probe micro-analysis (EPMA) measurements to provide geological insights on effectively determining (a) garnet end components and providing a format for further research on the type and genesis of the deposit; (b) the significance of the characteristic spectrum of garnet to the variation of mineralization environment; (c) the relationship between the characteristic spectrum of garnet and Fe/Al content; (d) the garnet characteristic spectrum to the economic mineralization. The results suggest that garnet characteristics of the thermal infrared spectrum can be used as an indicator for skarn deposit prospecting.

The Sinongduo mining region includes two types of mineralizations: the epithermal and the carbonate‐hosted Pb‐Zn‐Ag deposits. Despite being studied for many years, the ore formation process and genesis of the carbonate‐hosted Pb‐Zn‐Ag deposits remain poorly understood. The Pb‐Zn‐Ag ore bodies occur as veins and are hosted by limestone and dolostone of the Permian Xiala Formation. Three sulfide mineralization substages have been identified at the Sinongduo carbonate‐hosted deposit. Indium coupled with Cu, Co and Sn was incorporated into sphalerite as substitutions: 2Zn2+ ↔ Cu+ + In3+, (3n/2 + 1)Zn2+ ↔ Co2+ + nIn3+ or (2n + 1)Zn2+ ↔ Co2+ + n(Cu+ + In3+) (n > 1) and 4Zn2+ ↔ Sn2+ + 2In3+. Sphalerite and pyrite in the mineralization stage display δ34S values in a narrow range of +5.7‰ to +11.3‰, which are similar to those of Palaeocene igneous rocks, indicative of a magmatic source of sulfur. We present systematic carbon‐hydrogen‐oxygen isotope results that further support a magmatic source for the ore‐forming fluids that were influenced by meteoric water. Furthermore, the Pb isotope compositions of sulfide minerals in the Sinongduo carbonate‐hosted deposit overlap with the values of coeval Linzizong volcanic rocks and are similar to those of Indian Ocean sediments, indicating upper crustal sources of metals. We conclude that the Sinongduo carbonate‐hosted Pb‐Zn‐Ag deposit is a medium‐ to low‐temperature magmatic‐hydrothermal deposit related to Linzizong magmatism.