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Journal of Petrology Volume 41 Number 12 Pages 1721-1742 2000
© Oxford University Press 2000

Sulphide Segregation in Ferropicrites from the Pechenga Complex, Kola Peninsula, Russia

G. E. BRÜGMANN1,*, E. J. HANSKI2, A. J. NALDRETT3 and V. F. SMOLKIN4

1MAX-PLANCK-INSTITUT FÜR CHEMIE, ABT. GEOCHEMIE, POSTFACH 3060, 55020 MAINZ, GERMANY
2GEOLOGICAL SURVEY OF FINLAND, PO BOX 77, FIN-96101 ROVANIEMI, FINLAND
3DEPARTMENT OF GEOLOGY, UNIVERSITY OF TORONTO, TORONTO, ONT. M5S 3B1, CANADA
4GEOLOGICAL INSTITUTE, ACADEMY OF SCIENCES, SU-184200 APATITY, RUSSIA

The Palaeoproterozoic Ni–Cu sulphide deposits of the Pechenga Complex, Kola Peninsula, occur in the lower parts of ferropicritic intrusions emplaced into the phyllitic and tuffaceous sedimentary unit of the Pilgujärvi Zone. The intrusive rocks are comagmatic with extrusive ferropicrites of the overlying volcanic formation. Massive lavas and chilled margins from layered flows and intrusions contain <3–7 ng/g Pd and Pt and <0·02–2·0 ng/g Ir, Os and Ru with low Pd/Ir ratios of 5–11. The abundances of platinum group elements (PGE) correlate with each other and with chalcophile elements such as Cu and Ni, and indicate a compatible behaviour during crystallization of the parental magma. Compared with the PGE-depleted central zones of differentiated flows (spinifex and clinopyroxene cumulate zones) the olivine cumulate zones at the base contain elevated PGE abundances up to 10 ng/g Pd and Pt. A similar pattern is displayed in intrusive bodies, such as the Kammikivi sill and the Pilgujärvi intrusion. The olivine cumulates at the base of these bodies contain massive and disseminated Ni–Cu-sulphides with up to 2 µg/g Pd and Pt, but the PGE concentrations in the overlying clinopyroxenites and gabbroic rocks are in many cases below the detection limits. The metal distribution observed in samples closely representing liquid compositions suggests that the parental magma became sulphide saturated during the emplacement and depleted in chalcophile and siderophile metals as a result of fractional segregation of sulphide liquids. Relative sulphide liquid–silicate melt partition coefficients decrease in the order of Ir > Rh > Os > Ru > Pt = Pd > Cu. R-factors (silicate-sulphide mass ratio) are high and of the order of 104–105, and they indicate the segregation of only small amounts of sulphide liquid in the parental ferropicritic magma. In differentiated flows and intrusions the sulphide liquids segregated and accumulated at the base of these bodies, but because of a low silicate–sulphide mass ratio the sulphide liquids had a low PGE tenor and Pt/Ir and Cu/Ir ratios similar to the parental silicate melts. During cooling the sulphide liquid crystallized 40–50% of monosulphide solid solution (mss) and the residual sulphide liquid became enriched in Cu, Pt and Pd and depleted in Ir, Os and Ru. The Cu-rich sulphide liquid locally assimilated components of the surrounding S-rich sediments as suggested by the radiogenic Os isotopic composition of some sulphide ores ({gamma}Os > 100). Most of the massive and breccia ores represent mixtures of mss and residual Cu-rich sulphide liquid whereas chalcopyrite-rich veins formed when the Cu-rich sulphide liquids were squeezed out into the surrounding sediments.

KEY WORDS: ferropicrite; Pechenga; magmatic Ni–Cu sulphide deposits; platinum-group elements


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