Notes: Abstract The present investigation deals with sulphur isotope distribution in Lower Proterozoic iron and sulphide mineralizations in northern Sweden. The contrasting sulphur isotope patterns are indicative of different genesis. Some 267 sulphur isotope analyses of pyrite, pyrrhotite, chalcopyrite, sphalerite, galena and bornite from 23 occurrences have been performed. Some deposits exhibit uniform compositions, although the mean δ 34S values are clearly different, while other mineralizations have widely fluctuating values. The δ 34S values in syngenetic, exhalative sedimentary skarn iron ores, quartz-banded iron ores and sulphide mineralizations of the 2.0–2.5 Ga old (Lapponian) Greenstone group show a large spread, supporting the existence of bacteriogenic sulphate reduction processes. The spread of the sulphur isotope values (δ 34S = -8 to +25‰), and the non-equilibrium conditions, point to a biogenic rather than to an inorganic reduction of seawater sulphate. The isotopic composition of the sulphides in the epigenetic Lannavaara iron ores which were formed by a hydrothermal scapolite-tourmalme-related process, indicates a sulphur source similar to that of the Greenstone group. The δ 34S values of Cu-(Au) sulphide mineralizations in the Malmberget region (e.g. Aitik), which were formed by a similar process and hosted by the volcanics-volcanoclastics of the 1.9 Ga old Porphyry group, are slightly below zero ‰, indicating a magmatic origin. The existence of different sulphur compositions for these mineralization types formed by a similar hydrothermal process, probably reflects the influence of the host rock, the solutions leaching pre-existing sulphides. In southern Norrbotten, epigenetic, Cu-Zn-Pb veintype mineralizations in metavolcanics and metasediments have δ 34S values close to zero ‰ indicating a magmatic origin. The sulphur isotope data of the volcanogenic, massive sulphide ores of the Skellefte district, in particular the ores of the Adak dome, are close to zero ‰. The lead and sulphur isotopic features of the sulphides in northern Sweden show that the ore-forming processes were of a different nature on both sides of the Archean-Proterozoic border, implying differences in the crustal development. Lead isotopes show that lead was mobilized from specific sources on each side of the border. The sulphur of the sulphides in the Greenstone group in NE Sweden and Finland was introduced by sedimentary processes, whereas the sulphur of the sulphide occurrences towards the SW, mainly in the Porphyry group, is dominated by a magmatic sulphur component.

Notes: Abstract The initial lead isotopic composition of metamorphosed and tectonically reworked sulfide deposits is not always preserved, as sulfides easily change their lead isotopic composition through incorporation of lead derived from external fluids or redistribution and recrystallization of the deposit. Sulfide trace-lead and in cases even galena-lead from such deposits may show exceedingly radiogenic lead isotopic compositions. Thus, the initial lead isotopic composition has to be estimated from other minerals. Scapolite, which is a common phase in alteration haloes associated with epigenetic sulfide deposits in northern Sweden, has very low uranium-contents. Therefore, its trace-lead contents could preserve the initial isotopic composition of the ore-forming fluids. As scapolite is more resistant to recrystallization, it is more likely to reflect the original lead isotope signature of the deposit. This is illustrated using scapolite and sulfides from the Pahtohavare Cu-Au deposit in northern Sweden, which is hosted by Palaeoproterozoic mafic tuffites and graphitic schists and was affected by a mild thermal metamorphism during the Caledonian orogeny.