Fluid inclusions trapped in quartz veins hosted by a leucogneiss from the southern part of the Naxos Metamorphic Core Complex (Attic‐Cycladic‐Massif, Greece) were studied to determine the evolution of the fluid record of metamorphic rocks during their exhumation across the ductile/brittle transition. Three sets of quartz veins (V‐M2, V‐BD & V‐B) are distinguished. The V‐M2 and V‐BD are totally or, respectively, partially transposed into the foliation of the leucogneiss. They formed by hydrofracturing alternating with ductile deformation accommodated by crystal‐plastic deformation. The V‐B is discordant to the foliation and formed by fracturing during exhumation without subsequent ductile transposition. Fluids trapped during crystal–plastic deformation comprise two very distinct fluid types, namely a CO2‐rich fluid and a high‐salinity brine, that are interpreted to represent immiscible fluids generated from metamorphic reactions and the crystallization of magmas respectively. They were initially trapped at ∼625 °C and 400 MPa and then remobilized during subsequent ductile deformation resulting in various degrees of mixing of the two end‐members with later trapping conditions of ∼350 °C and 140 MPa. In contrast, brittle microcracks contain aqueous fluids trapped at 250 °C and 80 MPa. All veins display a similar δ13C pointing to carbon that was trapped at depth and then preserved in the fluid inclusions throughout the exhumation history. In contrast, the δD signature is marked by a drastic difference between (i) V‐M2 and V‐BD veins that are dominated by carbonic, aqueous‐carbonic and high‐salinity fluids of metamorphic and magmatic origin characterized by δD between −56‰ and −66‰, and (ii) V‐B veins that are dominated by aqueous fluids of meteoric origin characterized by δD between −40‰ and −46‰. The retrograde P–T pathway implies that the brittle/ductile transition separates two structurally, chemically and thermally distinct fluid reservoirs, namely (i) the ductile crust into which fluids originating from crystallizing magmas and fluids in equilibrium with metamorphic rocks circulate through a geothermal gradient of 30 °C km−1 at lithostatic pressure, and (ii) the brittle upper crust through which meteoric fluids percolate through a high geothermal gradient of 55 °C km−1 at hydrostatic pressure.

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International audienceThis contribution presents an original study combining detailed mapping, petrography, whole-rock geochemistry and geochronological constraints on the recently identified LREE (Light Rare Earth Elements) occurrences associated with pegmatitic granite dykes (PGD) from the central Grenville (Lac Okaopéo region). These PGD intrude paragneisses or meta-igneous complexes with a REE mineralization hosted either in monazite-(Ce) or in allanite-(Ce) respectively. The investigated samples display peraluminous signatures and are dominated by a quartz+K-feldspar+plagioclase+biotite+monazite/allanite assemblage. Field relationships and the magmatic textures of the dykes combined with U-Pb dating of magmatic monazite grains at 1005.4±4.4 Ma and 996.7±5.3 Ma (concordant igneous ages) imply that the LREE-rich PGD were emplaced in a post-tectonic setting. Allanite-(Ce) and monazite-(Ce)-bearing PGD have ΣREE contents up to 9242 ppm and 7048 ppm, respectively. The allanite-rich assemblage is consistent with the petrographic assemblage of LREE-enriched PGD identified in the southwestern Grenville Province and elsewhere in the world, but this study constitutes the first evidence for a sole presence of monazite as LREE-bearing phase in strongly peraluminous PGD from the Grenville Province

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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.

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