The Santa Rita gold deposit in the Proterozoic Paranoá Group, Goiás, Brazil: An example of fluid mixing during ore deposition
| Autor: | D. Michel, Gaston Giuliani, O.J. Marini, Gema R. Olivo |
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| Rok vydání: | 1993 |
| Předmět: |
ALTERATION HYDROTHERMALE
Sylvite Greenschist MINERALISATION Geochemistry GITOLOGIE Mineralogy Metamorphism OR Geology engineering.material RESULTAT ANALYTIQUE Hydrothermal circulation chemistry.chemical_compound chemistry GEOCHIMIE Geochemistry and Petrology engineering Carbonate Halite Economic Geology Pyrite Quartz |
| Zdroj: | Ore Geology Reviews. 8:503-523 |
| ISSN: | 0169-1368 |
| DOI: | 10.1016/0169-1368(93)90042-w |
| Popis: | The Santa Rita gold deposit (Central Goias, Brazil) is hosted by Middle to Upper Proterozoic carbonate-pelite sequences of the Paranoa Group that have been metamorphosed in the greenschist facies. The ore is contained in pyrite-bearing quartz-carbonate veins. The mineralization is structurally controlled by WNW-ESE high-angle faults and fractures resulting from the reactivation of older NE-SW lineaments. Pyrite is the sole sulphide and it shows growth zones enriched in Co, Ni and As (up to 4 wt%). Hydrothermal alteration zones are enriched in Co, Ni and As and are characterized by diffuse albitization, carbonatization, silicification and pyritization. A fluid inclusion study on quartz from pyrite-bearing quartz-carbonate veins led to the identification of two fluids: (1) a highly saline CO 2 N 2 -rich aqueous fluid with halite and ± sylvite daughter minerals, and (2) a CO 2 N 2 rich aqueous fluid with moderate salinity. The two fluid types occur in the same quartz domain and display great variation in the degree of filling and notable dispersion of the microthermometric data. On heating, all the inclusions decrepitate between 200° and 300°C. Raman spectrometry detected high concentrations of N 2 in the gas phase, with a CO 2 N 2 molar ratio between 1 and 19 and a small proportion of CH 4 (up to 2 mole %). The simultaneous entrapment of compositionally variable fluids in the system H 2 OCO 2 N 2 NaClKCl allow us to propose a mechanism of heterogeneous trapping. The entrapment may result from the mixing of a high-salinity fluid (H 2 ONaClKCl system) with a carbonic fluid (H 2 OCO 2 N 2 system) produced by the devolatilization process of carbonate and phyllitic host rocks. Considering the absence of spatially and temporally related igneous activity and the low P - T regional metamorphism in the Paranoa Group, the brines are inferred to result from leaching of evaporites occurring in the lower part of the Paranoa lithostratigraphic column. Gold was probably initially transported as an AuCl 2 -complex ( T >300°C, low pH, moderate ƒ O 2 - pyrite field stability). As temperature decreased below 290°C, the “switch-over” process would lead to the predominance of Au(HS) 2 − in the fluid. Pyrite precipitated in this temperature interval. The oscillatory zoning of the AsCoNi-bearing pyrites indicates episodic fluctuation of the fluid composition. Such changes in fluid composition are favoured by a mechanism of fluid mixing by intermittent supplies in the hydrothermal system. The proposed mechanism of heterogeneous trapping of two separate fluids in the system H 2 OCO 2 N 2 NaClKCl and the resulting changes in the physicochemical conditions caused by the fluid mixing appears as a conspicuous process for the Santa Rita hydrothermal fluid evolution. A model based on the existence of a Proterozoic geothermal system involving the regional thermal gradient is proposed. |
| Databáze: | OpenAIRE |
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