4.7 Article

In situ trace element and sulfur isotope of pyrite constrain ore genesis in the Shapoling molybdenum deposit, East Qinling Orogen, China

期刊

ORE GEOLOGY REVIEWS
卷 105, 期 -, 页码 123-136

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.oregeorev.2018.12.019

关键词

Pyrite; Trace element; Sulfur isotope; Shapoling Mo deposit; East Qinling

资金

  1. National Key Research and Development Program of China [2016YFC0600504]
  2. Fundamental Research Funds for the Central Universities [2652017276, 2652017218]
  3. Australian Geophysical Observing System (AGOS) by the AQ44 Australian Education Investment Fund
  4. Australian Microscopy and Microanalysis Research Facility
  5. AuScope
  6. Australian Science and Industry Endowment Fund
  7. State Government of Western Australia

向作者/读者索取更多资源

The Early Cretaceous (ca. 128 Ma) Shapoling vein-type molybdenum (Mo) mineralization, associated with the Huashan intrusion is a newly discovered deposit in the Xiong'ershan district, East Qinling, China where pyrite is a ubiquitous mineral phase. Here we present results from an integrated study on the texture, in situ trace element chemistry from laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) and sulfur isotopic composition using secondary-ion mass spectrometry (SIMS), with a view to understand the geochemical variation, genesis of Mo mineralization and ore-forming process. The distinct textural patterns as revealed by petrographic observations suggest three types of pyrites: Py1 is composed of coarse-grained euhedral pyrite in the wall rock and early barren quartz vein at Stage I, Py2 is represented by subhedral-anhedral grains coexisting with molybdenite in quartz veins at Stage II, and Py3 forms irregular interstitial grains in the quartz + K-feld-spar + molybdenite dominated veins at Stage III. The Mo enrichment mainly occurred in Py3 (with Co/Ni ratios > 1 and delta S-34 values mainly < 0 parts per thousand). Our study shows that Mo, Au, Pb, Zn, Ag and Cu are selectively partitioned into pyrite as mineral micro/nano-inclusions, and that the siderophile and chalcophile elements (such as Co, Ni, As, Se and Te) occur substituted within different textural types of pyrite. The delta S-34 values of the pyrites in Py1 and Py2 range between -2.33 parts per thousand and -0.37 parts per thousand, indicating a dominantly magmatic origin. The delta S-34 values of Py3 increase from -2.55 parts per thousand to +1.48 parts per thousand. In situ et analysis of pyrite from Py1, Py2 to Py3 shows a progressive and gradual change in redox conditions. The negative values indicate oxidized sulfur in the early generation of pyrite (Py1 that coexists with magnetite). Conversely, positive values represent reduced sulfur found in the later generations of pyrite (Py3), which contain higher concentrations of Cu, Pb, Zn and Ag. The Mobearing pyrite identified in our study could be used as a possible pathfinder for the exploration of high-grade Mo mineralization.

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