Browsing by Author "Velasquez-Ruiz, Felipe"

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    Microanalytical investigation of K-rich fenites from the Catalao II alkaline-carbonatite complex in Central Brazil: Implications for ore-forming processes within the world's largest niobium province
    (2024) Velasquez-Ruiz, Felipe; Reich, Martin; Cordeiro, Pedro; Lagoeiro, Leonardo; Angerer, Thomas
    Alkaline-carbonatite complexes are the main source of critical raw materials such as niobium (Nb) and rare earth elements (REE), which concentrate through a combination of magmatic and carbohydrothermal processes. These systems typically occur in close spatial connection with altered country rocks resulting from metasomatic alteration by exsolved K-Na-rich fluids, a process known as fenitization. Thus, the association between Nb-REE-rich carbonatites and fenites provides a unique opportunity for the investigation of carbohydrothermal alteration processes leading to critical metal enrichment. In this study, we focused on K-rich fenites associated with a shallow dike swarm system in the Boa Vista niobium deposit, the second-largest global producer of Nb, which is hosted within the Catal & atilde;o II alkaline-carbonatite complex in Central Brazil. We used a combination of micro-analytical techniques including EBSD, EMPA, and mu-EDXRF to unravel the complex micro-textural features of the fenites. Our data suggest that alkaline fluids exsolved vigorously from the carbonatite melts upon dike emplacement and pervasively metasomatized the country rocks, forming a melanocratic proximal fenite (phlogopitite), and distal fine-grained orthoclase-phlogopite-calcite fenites. Fluid alteration mobilized soluble cations (K, Fe, Mg, Ba, and Sr) plus S, CO2 and OH-, whereas Nb and REE were retained in the carbonatite dikes. The consistent dike-orthogonal orientation of metasomatic phlogopite and orthoclase grains in the proximal fenite, determined by EBSD, suggests that newly formed metasomatic minerals precipitated from the fenitizing fluids along the flow path. These orientations differ from the isotropic textures defined by primary (magmatic) minerals like pyrochlore, tetraferriphlogopite, dolomite, and calcite. However, and despite the microstructural differences between magmatic and carbohydrothermal phlogopite, their mineral chemistry is similar, suggesting that fenites are almost synchronous to the emplacement of carbonatites. These data indicate that fenites provide a rich archive of alkali-rich fluid infiltration around Nb-REE-rich carbonatite intrusions.
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    Origin of carbonatite-related niobium deposits: Insights from pyrochlore geochemistry
    (2024) Velasquez-Ruiz, Felipe; Reich, Martin; Broom-Fendley, Sam; Beard, Charles D.; Barra, Fernando; Romero, Rurik; Cordeiro, Pedro
    The carbonatite-related Nb deposits of the Alto Parana & iacute;ba Igneous Province (APIP) in central Brazil, currently account for similar to 92 % of the global Nb production. In the APIP, pyrochlore is abundant in magnet-ite-apatite-tetraferriphlogopite +/- carbonate rocks or phoscorites, occurring as interbedded layers with carbo-natites in the lower hypogene zone, feeding dike swarms of phoscorite and calcite carbonatite, and late-stage carbothermal veins in the upper hypogene zone. The origin of the phoscorite-carbonatite association can be explained by three hypotheses: (1) crystal segregation from fractional crystallization, (2) liquid immiscibility, and/or (3) phoscoritic magma formation after basement metasomatism (fenitization). However, it is not well understood whether pyrochlore formation is limited to a carbonatitic event, carbohydrothermal, or both, and this gap of knowledge is addressed in this work. To investigate the petrogenesis of pyrochlore-rich phoscorite, cathodoluminescence (CL) images, chemical maps, and LA-ICP-MS data were acquired of pyrochlore crystals from magmatic and carbothermal rocks from the Boa Vista Nb mine, Catalao II Complex. In the Boa Vista mine, oscillatory and patchy zoning were identified as primary pyrochlore textures commonly recorded at the lower hypogene zone, while secondary dissolution, skeletal and zonation-free textures are registered at shallower depths in the upper hypogene zone. Calciopyrochlore is the dominant Nb phase at the Boa Vista mine, with only two kenopyrochlore outliers. The pyrochlore CI chondrite-normalized REE distribution is consistent with geochemical results of the carbonatite and phoscorite rocks, indicating a magmatic origin for pyrochlore and the presence of pyrochlore antecrysts in carbothermal veins. The Sr/Y vs La and Na vs Ce diagrams in pyrochlore indicate a continuous fractionation pattern, with some mixtures of antecrysts and primary phases. An exami-nation of intercumulus calcite using CL provide evidence of carbonatitic magma residues within tetraferri-phlogopite phoscorite dikes and suggests that alkaline-carbonate-rich fluids played a role in transporting heavy minerals (i.e., magnetite, apatite, pyrochlore). Consequently, the textural and chemical evidence in the Boa Vista Nb mine indicates that the origin of pyrochlore-rich phoscorites is the result of physical segregation of heavy minerals from a carbonatite magma by fractional crystallization, leading to the emplacement of pyrochlore-rich carbonatite and phoscorite dikes. The implications at Catalao II may extend to other APIP alkaline-carbonatite complexes, as they share a genetic connection, and should motivate further studies focusing on pyrochlore geochemistry in other carbonatite-related Nb deposits, which will be crucial for advancing our knowledge of global Nb metallogenesis.