The Ak-Sug Porphyry Copper-Gold-Molybdenum Deposit, East Sayan: Noble Metal Mineralization, PT-Parameters, and Composition of Ore-Bearing Fluid

被引:1
作者
Kuzhuget, R. V. [1 ]
Ankusheva, N. N. [1 ,2 ]
Khertek, A. K. [1 ]
Mongush, A. O. [1 ]
Butanaeva, Yu. V. [1 ]
机构
[1] Russian Acad Sci, Tuvinian Inst Explorat Nat Resources, Siberian Branch, Kyzyl 667007, Russia
[2] Russian Acad Sci, South Urals Fed Res Ctr Mineral & Geoecol, Uralian Branch, Miass 456317, Chelyabinsk Obl, Russia
基金
俄罗斯科学基金会;
关键词
porphyry Cu-Au-Mo deposits; Au-Ag epithermal mineralization; porphyry-epithermal systems; quartz; fluid inclusions; stable isotopes; Tuva; CU-AU DEPOSIT; PLATINUM-GROUP ELEMENTS; PB ZIRCON AGE; RE-OS; U-PB; SOUTH URALS; ISOTOPE FRACTIONATION; MO DEPOSIT; ICP-MS; GEOCHRONOLOGY;
D O I
10.1134/S1075701523070188
中图分类号
P5 [地质学];
学科分类号
0709 ; 081803 ;
摘要
Ore mineralization of the Ak-Sug Porphyry Copper-Gold-Molybdenum deposit formed during three stages: 1) porphyry-copper mineralization with simple sulfides in quartz-sericite and quartz-sericite-chlorite metasomatites, 2) subepithermal Au-Bi-Te-Pd-quartz mineralization in quartz-sericite metasomatites, and 3) intermediate-sulfidation Au-Ag mineral assemblages with selenides, tellurides, and Sb and As sulfosalts in argillisites. Fluid inclusion studies (microthermometry, Raman spectroscopy) of quartz and mineral thermometry (an assemblage of Au and Ag tellurides) showed that porphyry copper and subepithermal mineralization precipitated from hydrocarbon-aqueous-chloride (Na-K +/- Fe) fluid with salinity of 20.1-32.8 wt % NaCl eq. at 435-375 degrees C and hydrocarbon-aqueous-chloride (Na-K +/- Fe +/- Ca +/- Mg) fluid with salinity of 7.5-15.0 wt % NaCl eq. at 415-325 degrees C, respectively. The epithermal mineral assemblages precipitated at similar to 0.55 kbar from hydrocarbon-aqueous-chloride (Na-K +/- Fe +/- Ca +/- Mg) fluid with salinity of 1.4-12.6 wt % NaCl eq. at 370-200 degrees C. The latest low-temperature (240-190 degrees C) and diluted (3.5-4.9 wt %) fluids are characterized by variations in Na and K chlorides; Fe2+, Fe3+, Ca, and Mg carbonates; and Na, K, and Mg sulfates. The S isotopic composition of the fluid of different mineral assemblages varies from -2.7 to +0.3 parts per thousand and suggest that they are derivatives of a single porphyry system. The delta 18O values of the fluid of porphyry copper (7.4 parts per thousand) and subepithermal (7.0 parts per thousand) stages indicate its magmatic genesis, whereas those of the epithermal stage (from +1.2 to +7.2 parts per thousand) are evident of mixing of magmatic fluid and meteoric waters (from +0.4 to +5.7 parts per thousand). Our isotopic data, combined with mineralogical-geochemical peculiarities and formation conditions of ores, provide tracing the principles of the evolution of mineral assemblages, temperatures, composition, and fluid salinity at the Ak-Sug deposit upon the transition from porphyry copper to epithermal stage.
引用
收藏
页码:S58 / S84
页数:27
相关论文
共 107 条
[1]   PHASE-RELATIONS AMONG TELLURIDES, SULFIDES, AND OXIDES .1. THERMOCHEMICAL DATA AND CALCULATED EQUILIBRIA [J].
AFIFI, AM ;
KELLY, WC ;
ESSENE, EJ .
ECONOMIC GEOLOGY, 1988, 83 (02) :377-394
[2]  
Atkinson A. B., 2002, MSc thesis
[3]   On the origin of the pge mineralization in the elatsite porphyry Cu-Au deposit, Bulgaria:: Comparison with the Baula-Nuasahi complex, India, and other alkaline PGE-rich porphyries [J].
Augé, T ;
Petrunov, R ;
Bailly, L .
CANADIAN MINERALOGIST, 2005, 43 :1355-1372
[4]  
Baksheev I.A., 2014, METALLOGENIYA DREVNI, P108
[5]  
Beane R.E., 1983, Special Report, V13, P245
[6]  
Berger B.R., 1989, EC GEOLOGY MONOGRAPH, V6, P405
[7]  
Berzin N.A., 1994, Russ. Geol. Geophys., V35, P5
[8]  
Berzin N.A., 1996, Russian Geology and Geophysics, V37, P56
[9]  
Berzina A.N., 2003, Mineral Exploration and Sustainable Development
[10]   Paleozoic-Mesozoic Porphyry Cu(Mo) and Mo(Cu) Deposits within the Southern Margin of the Siberian Craton: Geochemistry, Geochronology, and Petrogenesis (a Review) [J].
Berzina, Anita N. ;
Berzina, Adel P. ;
Gimon, Victor O. .
MINERALS, 2016, 6 (04)