Elevated Magmatic Chlorine and Sulfur Concentrations in the Eocene-Oligocene Machangqing Cu-Mo Porphyry Systems

Author:

Xu Bo123,Hou Zeng-qian4,Griffin William L.3,Zhou Ye1,Zhang Yu-Fei1,Lu Yong-Jun5,Belousova Elena3,Xu Ji-Feng1,O’Reilly Suzanne Y.3

Affiliation:

1. 1State Key Laboratory of Geological Processes and Mineral Resources, China University of Geosciences, Beijing 100083, China

2. 2Beijing SHRIMP Center, CAGS, Beijing 100037, China

3. 3ARC Centre of Excellence for Core to Crust Fluid Systems (CCFS) and GEMOC, Macquarie University, NSW 2109, Australia

4. 4Chinese Academy of Geological Sciences, Beijing 100037, China

5. 5Geological Survey of Western Australia, 100 Plain Street, East Perth, WA 6004, Australia

Abstract

Abstract The Machangqing porphyry Cu-Au deposit is located in the Sangjiang region, Jinshajiang-Ailaoshan metallogenic belt, southeastern Tibet. It has three main phases of felsic-mafic intrusions: barren granites, ore-forming porphyry intrusions, and mafic lamprophyres. U-Pb zircon dating shows that these intrusions were emplaced over a period of ~3 m.y., with lamprophyres at 36.50 ± 1.6 Ma (1σ), porphyry intrusion at 34.26 ± 0.22 Ma (1σ), and granite intruded at 34.00 ± 0.26 Ma (1σ). The in situ Rb-Sr analysis of phlogopite and amphibole, primary minerals in the lamprophyres, also gives a date of 36.5 ± 1.5 Ma (2σ), regarded as the emplacement age of the lamprophyre, earlier than the ore-forming porphyry intrusions. The magmatic phases have significantly different sulfur and chlorine contents. The SO3 contents of igneous apatite microphenocrysts from the mineralization-related porphyry intrusions are higher (0.24 ± 0.14 wt %, 1σ, n = 82) than those from the barren granites (0.08 ± 0.07 wt %, 1σ, n = 30). The chlorine contents in apatite grains from the porphyry intrusions (0.18 ± 0.16 wt %, 1σ) are also higher than those from granites (0.04 ± 0.02 wt % Cl, 1σ). The apatite in lamprophyres have higher sulfur (0.68 ± 0.19 wt %, 1σ, n = 40) and chlorine (0.48 ± 0.13 wt %, 1σ). The large difference of Cl and S in lamprophyres might suggest that elevated magmatic volatile contents derived from the mafic magma were important for ore formation in the Machangqing porphyry systems. The in situ Sr and O isotopes in apatite phenocrysts from the porphyry intrusions (87Sr/86Sr: 0.70593–0.70850; δ18O: 6.0–7.0) are similar to those in the lamprophyres (87Sr/86Sr: 0.70595–0.70964; δ18O: 5.4–6.9), consistent with similar origins for their volatile contents. These data may indicate that the deeper magma chamber was recharged by a relatively S-Cl-rich mafic magma similar to the lamprophyres, triggering the ore-forming magmatic event. This study also suggests that origin of apatite Sr and also volatile contents, combined with in situ Sr and O isotopes, could be useful for fingerprinting fertile intrusions associated with mineralization within drainage source areas or in outcrops.

Publisher

Society of Economic Geologists

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