40 research outputs found

    Magmatic and hydrothermal behavior of uranium in syntectonic leucogranites: The uranium mineralization associated with the Hercynian Guérande granite (Armorican Massif, France)

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    Most of the hydrothermal uranium (U) deposits from the European Hercynian belt (EHB) are spatially associated with Carboniferous peraluminous leucogranites. In the southern part of the Armorican Massif (French part of the EHB), the GuĂ©rande peraluminous leucogranite was emplaced in an extensional deformation zone at ca. 310 Ma and is spatially associated with several U deposits and occurrences. The apical zone of the intrusion is structurally located below the Pen Ar Ran U deposit, a perigranitic vein-type deposit where mineralization occurs at the contact between black shales and Ordovician acid metavolcanics. In the MĂ©tairie-Neuve intragranitic deposit, uranium oxide-quartz veins crosscut the granite and a metasedimentary enclave. Airborne radiometric data and published trace element analyses on the GuĂ©rande leucogranite suggest significant uranium leaching at the apical zone of the intrusion. The primary U enrichment in the apical zone of the granite likely occurred during both fractional crystallization and the interaction with magmatic fluids. The low Th/U values (18Owhole rock = 9.7–11.6‰ for deformed samples and ÎŽ18Owhole rock = 12.2–13.6‰ for other samples) indicate that the deformed facies of the apical zone underwent sub-solidus alteration at depth with oxidizing meteoric fluids. Fluid inclusion analyses on a quartz comb from a uranium oxide-quartz vein of the Pen Ar Ran deposit show evidence of low-salinity fluids (1–6 wt.% NaCl eq.), in good agreement with the contribution of meteoric fluids. Fluid trapping temperatures in the range of 250–350 °C suggest an elevated geothermal gradient, probably related to regional extension and the occurrence of magmatic activity in the environment close to the deposit at the time of its formation. U-Pb dating on uranium oxides from the Pen Ar Ran and MĂ©tairie-Neuve deposits reveals three different mineralizing events. The first event at 296.6 ± 2.6 Ma (Pen Ar Ran) is sub-synchronous with hydrothermal circulations and the emplacement of late leucogranitic dykes in the GuĂ©rande leucogranite. The two last mineralizing events occur at 286.6 ± 1.0 Ma (MĂ©tairie-Neuve) and 274.6 ± 0.9 Ma (Pen Ar Ran), respectively. Backscattered uranium oxide imaging combined with major elements and REE geochemistry suggest similar conditions of mineralization during the two Pen Ar Ran mineralizing events at ca. 300 Ma and ca. 275 Ma, arguing for different hydrothermal circulation phases in the granite and deposits. Apatite fission track dating reveals that the GuĂ©rande granite was still at depth and above 120 °C when these mineralizing events occurred, in agreement with the results obtained on fluid inclusions at Pen Ar Ran. Based on this comprehensive data set, we propose that the GuĂ©rande leucogranite is the main source for uranium in the Pen Ar Ran and MĂ©tairie-Neuve deposits. Sub-solidus alteration via surface-derived low-salinity oxidizing fluids likely promoted uranium leaching from magmatic uranium oxides within the leucogranite. The leached out uranium may then have been precipitated in the reducing environment represented by the surrounding black shales or graphitic quartzites. As similar mineralizing events occurred subsequently until ca. 275 Ma, meteoric oxidizing fluids likely percolated during the time when the GuĂ©rande leucogranite was still at depth. The age of the U mineralizing events in the GuĂ©rande region (300–275 Ma) is consistent with that obtained on other U deposits in the EHB and could suggest a similar mineralization condition, with long-term upper to middle crustal infiltration of meteoric fluids likely to have mobilized U from fertile peraluminous leucogranites during the Late Carboniferous to Permian crustal extension events

    Carbonate alteration associated with talc-chlorite mineralization in the eastern Pyrenees, with emphasis on the St. Barthelemy Massif

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    International audienceThe eastern Pyrenees host a large number of talc-chlorite mineralizations of Albian age (112­97?Ma), the largest of which occur in the St. Barthelemy massif. There talc develops by hydrothermal replacement of dolostones, which were formed by alteration of calcite marbles. This alteration is progressive. Unaltered calcite marbles have oxygen isotope composition of about 25 (V-SMOW). The d18O values decrease down to values of 12 towards the contact with dolostones. This 18O depletion is accompanied by Mg enrichment, LREE fractionation and systematic shifts in the Sr isotope compositions, which vary from 87Sr/86Sr = 0.7087­0.7092 in unaltered calcite marbles to slightly more radiogenic compositions with 87Sr/86Sr = 0.7094 near dolomitization fronts. Dolostones have d18O values (about 9) lower than calcitic marbles, higher REE content and more radiogenic Sr isotope composition (87Sr/86Sr = 0.7109 to 0.7130). Hydrothermal calcites have d18O values close to dolostones but substantially lower d13C values, down to -6.5, which is indicative of the contribution of organic matter. The REE content of hydrothermal calcite is one order of magnitude higher than that of calcitic marbles. Its highly radiogenic Sr composition with 87Sr/86Sr = 0.7091 to 0.7132 suggests that these elements were derived from silicate rocks, which experienced intense chlorite alteration during mineralization. The chemical and isotopic compositions of the calcite marbles, the dolostones and the hydrothermal calcites are interpreted as products of successive stages of fluid-rock interaction with increasing fluid-rock ratios. The hydrothermal quartz, calcite, talc and chlorite are in global mutual isotopic equilibrium. This allows the calculation of the O isotope composition of the infiltrating water at 300?°C, which is in the d18O = 2­4.5 range. Hydrogen isotope compositions of talc and chlorite indicate a dD = 0 to -20. This water probably derived from seawater, with minor contribution of evolved continental wate

    Element distribution in the root zone of ultramafic-hosted black smoker-like systems: Constraints from an Alpine analog

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    Fluid-rock interactions at Mid-Oceanic Ridges lead to metal deposition in the so-called seafloor massive sulfides at ultramafic-hosted systems. Due to restricted access to the seafloor and scarcity of 3D exposures, these systems are poorly understood at-depth. A way to access the vertical dimension is to focus on fossil analogs preserved on-land such as the one preserved in serpentinites from the Platta nappe (SE Switzerland). For this example, we document the element distribution in the mineralized rocks at three distinct levels in the rock column using both whole rock chemical analyses and LA-ICPMS analysis of sulfide (chalcopyrite and pyrrhotite) and magnetite. We bring, for the first time, chemical signatures of the mineralization in the root zone of ultramafic-hosted black smokers. At any given depth, the Co/Ni ratio is maximum in the most mineralized samples indicating that this ratio is linked to the intensity of hydrothermal alteration. Additionally, the Co/Ni ratio decreases in mineralized rocks towards the paleosurface, whereas the Se content increases. An episode of carbonation recorded in the highest structural level of the system was responsible for a slight remobilization of the former Cu stock. We propose a model in which the uprising mineralizing fluid mixed with seawater within the host serpentinites, before venting at the paleoseafloor
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