期刊
MINERALIUM DEPOSITA
卷 44, 期 8, 页码 849-866出版社
SPRINGER
DOI: 10.1007/s00126-009-0252-4
关键词
Rutile; El Teniente; Porphyry copper deposit; Molybdenum; Chile
资金
- Chilean FONDECYT [198-0511, 800-0006]
Mineralogical, textural, and chemical analyses (EPMA and PIXE) of hydrothermal rutile in the El Teniente porphyry Cu-Mo deposit help to better constrain ore formation processes. Rutile formed from igneous Ti-rich phases (sphene, biotite, Ti-magnetite, and ilmenite) by re-equilibration and/or breakdown under hydrothermal conditions at temperatures ranging between 400A degrees C and 700A degrees C. Most rutile nucleate and grow at the original textural position of its Ti-rich igneous parent mineral phase. The distribution of Mo content in rutile indicates that low-temperature (similar to 400-550A degrees C), Mo-poor rutile (5.4 A +/- 1.1 ppm) is dominantly in the Mo-rich mafic wallrocks (high-grade ore), while high-temperature (similar to 550-700A degrees C), Mo-rich rutile (186 A +/- 20 ppm) is found in the Mo-poor felsic porphyries (low-grade ore). Rutile from late dacite ring dikes is a notable exception to this distribution pattern. The Sb content in rutile from the high-temperature potassic core of the deposit to its low-temperature propylitic fringe remains relatively constant (35 A +/- 3 ppm). Temperature and Mo content of the hydrothermal fluids in addition to Mo/Ti ratio, modal abundance and stability of Ti-rich parental phases are key factors constraining Mo content and provenance in high-temperature (a parts per thousand yen550A degrees C) rutile. The initial Mo content of parent mineral phases is controlled by melt composition and oxygen fugacity as well as timing and efficiency of fluid-melt separation. Enhanced reduction of SO2-rich fluids and sulfide deposition in the Fe-rich mafic wallrocks influences the low-temperature (a parts per thousand currency sign550A degrees C) rutile chemistry. The data are consistent with a model of fluid circulation of hot (> 550A degrees C), oxidized (AE'O-2 a parts per thousand yenaEuro parts per thousand NNO + 1.3), SO2-rich and Mo-bearing fluids, likely exsolved from deeper crystallizing parts of the porphyry system and fluxed through the upper dacite porphyries and related structures, with metal deposition dominantly in the Fe-rich mafic wallrocks.
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