CALL FOR PROPOSALS:

ORGANIZERS

  • Harvey Thorleifson, Chair
    Minnesota Geological Survey
  • Carrie Jennings, Vice Chair
    Minnesota Geological Survey
  • David Bush, Technical Program Chair
    University of West Georgia
  • Jim Miller, Field Trip Chair
    University of Minnesota Duluth
  • Curtis M. Hudak, Sponsorship Chair
    Foth Infrastructure & Environment, LLC

 

Paper No. 9
Presentation Time: 11:00 AM

IN SITU COPPER ISOTOPIC ANALYSIS OF SULFIDE MINERALS IN HYDROTHERMAL ORE DEPOSITS AND IGNEOUS ROCKS BY FEMTOSECOND LA-MC-ICP-MS


IKEHATA, Kei1, ISHIBASHI, Junichiro2, SUZUKI, Ryohei2, SHIMIZU, Hiroshi3, MATSUSHIMA, Takeshi3, MATSUMOTO, Satoshi3, UEHIRA, Kenji3 and HIRATA, Takafumi4, (1)Faculty of Life and Environmental Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, 305-8572, Japan, (2)Department of Earth and Planetary Sciences, Faculty of Sciences, Kyushu University, Fukuoka, 812-8581, Japan, (3)Institute of Seismology and Volcanology, Faculty of Sciences, Kyushu University, 2-5643-29 Shin'yama, Shimabara, 855-0843, Japan, (4)Division of Earth and Planetary Sciences, Graduate School of Science, Kyoto University, Kyoto, 606-8502, Japan, ikkei@geol.tsukuba.ac.jp

We investigated copper isotopic variations of sulfide chimney samples from two seafloor hydrothermal sites in the southern Mariana Trough by femtosecond-pulsed laser ablation multiple collector inductively coupled plasma mass spectrometry (fs-LA-MC-ICP-MS). The δ65Cu (where δ65Cu = [(65Cu/63Cu)sample/ (65Cu/63Cu)NIST-SRM976-1] × 1000) values of Cu-rich sulfide minerals of both sites are significantly large (-0.70 to 4.0‰) compared to those of Cu-rich minerals in ancient submarine hydrothermal deposits at mid-oceanic ridge settings (e.g., Besshi-type volcanogenic massive sulfide deposit, Japan, -0.31 to 0.26‰; Ikehata et al., 2011) and in mantle peridotite (Horoman, Japan) and island-arc volcanic rocks (e.g., Shinmoedake volcano, Japan)(-0.10 to 0.40‰).

These large copper isotopic variations in the chimney samples are most likely explained in terms of a redox-controlled isotope fractionation during hydrothermal reworking of copper sulfides below sea floor or alteration of primary hydrothermal copper sulfides by seawater (possibly by bacteria), involving the preferential incorporation of heavy copper isotopes in secondary Cu(II) solutions. These results also suggest that sub-seafloor recrystallization and metamorphic reequilibration may have reduced the original range of copper isotopes.

Therefore, copper isotopic geochemistry might be a useful tool for understanding details of ore-forming processes. However, further improvements in precision and accuracy of in situ copper isotopic analysis are needed to fully understand the copper isotopic behavior during high-temperature processes.

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