Mineralogical, lithogeochemical and sulfide trace element characteristics of the Hirvilavanmaa Au-only and the base metal-rich Naakenavaara orogenic gold deposits in the Central Lapland belt, northern Finland

Abstract The Hirvilavanmaa (Au-only) and Naakenavaara (Cu-Co-Au-Ni) deposits, located only 5 km apart in the Paleoproterozoic Central Lapland belt (CLB) in northern Finland, represent two types of orogenic gold mineralization that dominate the CLB: (1) Au-only and (2) Au with atypical metal association, respectively. In this study, we compare these deposits in order to pinpoint the origin of differences in their metal associations. The pyrite-rich Hirvilavanmaa and the pyrrhotite- and chalcopyrite-rich Naakenavaara deposits are hosted primarily by ultramafic metavolcanic and metasedimentary rocks respectively. Similarities in the deposits include pre-ore albitization of host rocks and ore mineralization-related carbonate and chlorite alteration and quartz‑carbonate veins. Ore-related sericite and biotite alteration is prominent only at Naakenavaara. Pyrite and chalcopyrite from the two deposits have a distinct trace element geochemistry; pyrrhotite from Naakenavaara hosts significant Co and Ni concentrations. At Hirvilavanmaa, three pyrite generations with distinct Co/Ni ratios represent the gradual evolution of ore deposition. Hirvilavanmaa can be confidently classified as an orogenic Au deposit with evidence pointing to a mafic metavolcanic rock source for the ore-forming components. At Naakenavaara, our results reveal a complex evolution involving two distinct but spatially coincident mineralizing events. The earliest base metal-rich event started as Co-rich and gradually developed into the main Cu-rich stage; two pyrite types (mean Co/Ni ratios of 12.5 and 762 respectively) are associated with these stages. Subsequently ore zones were overprinted locally by an orogenic Au event that deposited pyrite with low Co/Ni ratios (mean of 0.3). The presence of late gold deposition overprinting earlier base metal-rich ore fits with observations from other base metal‑gold deposits from northern Finland

From oil digger to energy transition enabler:the critical role of exploration geosciences education in Europe

Abstract Recent disruptions of raw material value chains during the COVID-19 pandemic have highlighted Europe’s depency on imports of metals and minerals. Meanwhile, the European Commission is establishing ambitious policy initiatives, aiming at making Europe climate neutral in 2050. In this contribution, we emphasise the critical role of geosciences education in this energy transition, in forming the next generation of mining professionals. In the Nordic countries, active industry–university collaboration in one of the most active mining hubs in Europe has allowed frequent student–industry interaction, access to real-life learning environments, and development of specialised educational modules. These have been made accessible to exchange students from other European countries via exchange programmes and innovative digipedagogical learning tools

Epigenetic gold occurrence in a Paleoproterozoic meta-evaporitic sequence in the Rompas-Rajapalot Au system, Peräpohja belt, northern Finland

Abstract The Rompas-Rajapalot gold prospect is located in the northern part of the Paleoproterozoic Peräpohja belt. It covers an area of at least 10 × 10 km and comprises various styles of gold mineralization ranging from localized high-grade Au pockets in uraninite- and pyrobitumen-bearing calcsilicate-carbonate-quartz veins in mafic metavolcanic rocks (Rompas area) to disseminated gold grains in Fe-Mg-rich metasediments and quartz-tourmaline-sulfide-native gold veins (Palokas area). This study deals with the petrography and mineral chemistry of the gold mineralization at Palokas, which occurs in the eastern part of the Rompas-Rajapalot prospect. Major and trace element data and fluid inclusion characteristics of tourmaline are used to evaluate the origin and the pressure-temperature-fluid composition parameters of hydrothermal fluids. Whole-rock geochemical analyses are utilized to evaluate the nature of the protolith of the host rocks. Gold occurs in a native form in at least two different textural settings: 1) single, relatively coarse grains disseminated among the rock-forming silicates in cordierite-orthoamphibole rocks and 2) smaller grains occurring in fractures of tourmaline in quartz-sulfide-tourmaline breccias and in fractures of chloritized cordierite-orthoamphibole rocks adjacent to the tourmaline-rich breccias. Fracture-related gold is associated with Bi-Se-S-bearing tellurides, native Bi, molybdenite, chalcopyrite, and pyrrhotite. Coarser-grained disseminated gold were not found to be clearly associated with sulfides nor any fractures. Statistical correlations show that the Au concentration correlates strongly with Te, Cu, Co, Se, Bi, Mo, and Ag (ρ = 0.730–0.619) whereas Au correlates moderately with As, Fe, W (ρ = 0.523–0.511) and to a lesser extent with U, Pb, and Ni (ρ = 0.492–0.407). Gold has the strongest negative correlations with Sr and Ca. The chondrite-normalized REE patterns of tourmaline from the Au-mineralized rocks (both vein type and host-rock tourmaline) and the late- to post-orogenic granite partly overlap and show similar LREE-enriched trends, with the enrichment being lower in tourmaline from the granite. Fluid inclusion studies from tourmaline in gold-bearing quartz-tourmaline-sulfide veins indicate that the veins were formed from H₂O-Na₂O-CO₂-CH₄-(H₂S) fluids in a boiling system under pressure conditions ranging from lithostatic to hydrostatic, with the depth being ~5 km and the temperature ~300°C. The properties of the ore-forming fluids support the genetic link between the late- to post-orogenic granitoid magmatism at ~1.78 Ga and the formation of the fracture-hosted gold mineralization, suggested based on earlier studies (including Re-Os-molybdenite age and boron isotope data from tourmaline). Based on the whole-rock geochemistry, it is highly plausible that the cordierite-orthoamphibole rocks and interlayered calcsilicatealbite rocks are part of a basin-wide lacustrine, at least partly evaporitic, sequence. The protolith of the cordierite-orthoamphibole rock was most probably a lake-margin sedimentary pile with abundant Mg-rich clays

Paleoproterozoic Rajapalot Au-Co system associated with evaporites:chemical composition and boron isotope geochemistry of tourmaline, and sulfur isotopes of sulfates, Peräpohja belt, northern Finland

Abstract The Raja Au-Co mineralization in the Paleoproterozoic Peräpohja belt in northern Finland is part of the wider Rompas-Rajapalot mineralized area with several known Au-Co occurrences. The area is characterized by distinct tourmaline occurrences, spatially associated with Au-Co mineralization. Four texturally distinct tourmaline types were identified although all analysed tourmalines belong to the alkali-group and are classified as dravite. δ ¹¹B values and fractionation modelling indicates that at least two distinct fluids were responsible for the tourmaline formation with initial end member δ¹¹B values of the fluids at −8‰ and −1‰. Possible sources for boron rich fluids are Svecofennian orogeny related (ca. < 1.9 Ga) metamorphic fluids and magmatic-hydrothermal fluids related to the late-orogenic ca. 1.78 Ga granitoids. Structural data from the quartz-tourmaline veins outlines a strong linear trend towards the Raja high-grade mineralization trend. This is interpreted as evidence for structural control of the Raja mineralization, which possibly is contained in shear-zones or within the hinge regions of local high degree folding. A distinctive rock unit with bright purple anhydrite layers and white gypsum veins has been intersected by drilling. While the sulfate-rich unit is unmineralized, the mineralogy and regional geological setting suggests an evaporitic origin. Anhydrite has δ³⁴S values in a narrow range from 8.1 to 9.8 ‰. Gypsum has slightly heavier δ³⁴S from 10.6 to 12.2 ‰. Together with isotope fractionation constraints, textural evidence suggests the authigenic formation of gypsum with SO₄²⁻ sourced from anhydrite. Significant similarities in textures and sulfur isotope values to well-known evaporite successions of the Onega basin, western Russia, further supports the presence of evaporitic strata within the Peräpohja belt

Sulphide trace element, sulphur isotope and hydrothermal alteration studies in the Juomasuo and Hangaslampi Au-Co deposits, Kuusamo belt, northeastern Finland

Abstract The Juomasuo and Hangaslampi Au-Co deposits are hosted by the Paleoproterozoic Kuusamo belt in northeastern Finland. Sulphur isotope and trace element data from sulphides indicate that the geochemically distinct, Au-Co and Co-only enrichments were formed from fluids of different origin. Accordingly, sericite alteration is typical in the zones of the Au-Co enrichment, whereas the chlorite-biotite-amphibole alteration occurs in relation to the Co-only mineralization. Variation in the composition of host rocks does not seem to have a strong control on the type of mineralization

Kivilompolo Mo mineralization in the Peräpohja belt revisited:trace element geochemistry and Re-Os dating of molybdenite

Abstract The Kivilompolo molybdenite occurrence is located in the northern part of the Peräpoh jabelt, within the lithodemic Ylitornio nappe complex. It is hosted within a deformed porphyritic granite belonging to the pre-orogenic 1.99 Ga Kierovaara suite. The mineralization occurs mostly as coarse-grained molybdenite flakes in boudinaged quartz veins, with minor chalcopyrite, pyrite, magnetite, and ilmenite. In this study, we report new geochemical data from the host-rock granite and Re-Os dating results of molybdenite from the mineralization. For the whole-rock geochemistry, the mineralized granite is similar to the Kierovaara suite granites analyzed in previous studies. Also, the ca. 2.0 Ga Re-Os age for molybdenite is equal, within error, to the U-Pb zircon age of the Kierovaara suite granite. In addition, similar molybdenite and uraninite ages have been reported from the Rompas-Rajapalot Au-Co occurrence located 30 km NE of Kivilompolo. We propose that the magmatism at around 2.0 Ga ago initiated the hydrothermal circulation that was responsible for the formation of the molybdenite mineralization at Kivilompolo and the primary uranium mineralization associated with the Rompas-Rajapalot Au-Co occurrence or at least, the magmas provided heating, and in addition potentially saline magmatic fluids and metals from a large, cooling magmatic-hydrothermal system

Geochemical signatures of mineralizing events in the Juomasuo Au–Co deposit, Kuusamo belt, northeastern Finland

Abstract The Juomasuo Au–Co deposit, currently classified as an orogenic gold deposit with atypical metal association, is located in the Paleoproterozoic Kuusamo belt in northeastern Finland. The volcano-sedimentary sequence that hosts the deposit was intensely altered, deformed, and metamorphosed to greenschist facies during the 1.93–1.76 Ga Svecofennian orogeny. In this study, we investigate the temporal relationship between Co and Au deposition and the relationship of metal enrichment with protolith composition and alteration mineralogy by utilizing lithogeochemical data and petrographic observations. We also investigate the nature of fluids involved in deposit formation based on sulfide trace element and sulfur isotope LA-ICP-MS data together with tourmaline mineral chemistry and boron isotopes. Classification of original protoliths was made on the basis of geochemically immobile elements; recognized lithologies are metasedimentary rocks, mafic, intermediate-composition, and felsic metavolcanic rocks, and an ultramafic sill. The composition of the host rocks does not control the type or intensity of mineralization. Sulfur isotope values (δ³⁴S − 2.6 to + 7.1‰) and trace element data obtained for pyrite, chalcopyrite, and pyrrhotite indicate that the two geochemically distinct Au–Co and Co ore types formed from fluids of different compositions and origins. A reduced, metamorphic fluid was responsible for deposition of the pyrrhotite-dominant, Co-rich ore, whereas a relatively oxidized fluid deposited the pyrite-dominant Au–Co ore. The main alteration and mineralization stages at Juomasuo are as follows: (1) widespread albitization that predates both types of mineralization; (2) stage 1, Co-rich mineralization associated with chlorite (± biotite ± amphibole) alteration; (3) stage 2, Au–Co mineralization related to sericitization. Crystal-chemical compositions for tourmaline suggest the involvement of evaporite-related fluids in formation of the deposit; boron isotope data also allow for this conclusion. Results of our research indicate that the metal association in the Juomasuo Au–Co deposit was formed by spatially coincident and multiple hydrothermal processes