Microchemistry and stable isotope systematics of gold mineralization in a gabbro-diorite complex, SE Egypt

Basem Ahmed Zoheir*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

Electron probe micro-analysis (EPMA) and laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) data of ore minerals from the Um Eleiga deposit (SE Egypt) suggest that primary Au was sequestered within Ni-pyrrhotite and Co-Ni-Fe sulfarsenide, while refined, free-milling gold grains (~. 93. wt.% Au) are associated with late pyrite, or occur along micro-fractures in quartz veins. A magmatic source of gold is most likely, yet endowment by circulating metasomatic fluid was crucial for Au concentration.Sulfur stable isotope values (δ 34S) of sulfide minerals disseminated in the quartz veins (pyrite: -0.5 to 1.5‰, chalcopyrite: -0.3 to 0.6‰, and sphalerite: -0.1 to -0.4‰), indicate a generally light sulfur source. Similarly, measured δ 13C of vein calcite (-3.1 to -1.8, n=9) and calculated fluid δ 13C CO2 values (-0.6 to 0.6‰, for the temperature range 350-375°C of associated hydrothermal chlorite) cluster around 0‰, consistent with a magmatic source for carbon. Oxygen isotope data for vein calcite (10.3-13‰, n=9) and quartz (11.7-14.3‰, n=10) indicate average fluid δ 18O H2O values of 7.4 and 7.8‰, respectively, which implicate fluids similar to those in intrusion-related systems.

Original languageEnglish
Pages (from-to)148-157
Number of pages10
JournalMicrochemical Journal
Volume103
DOIs
StatePublished - Jul 2012
Externally publishedYes

Keywords

  • Egypt
  • Island arc intrusive complex
  • Microchemistry
  • Stable isotopes
  • Um Eleiga gold deposit

ASJC Scopus subject areas

  • Analytical Chemistry
  • Spectroscopy

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