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Geochemical and spectroscopic investigation of apatite in the Siilinjärvi carbonatite complex: Keys to understanding apatite forming processes and assessing potential for rare earth elements

Authors :
Vinciane Debaille
Jean-Marc Baele
Hartwig E. Frimmel
Mikko Savolainen
Stefan Höhn
Julien Mercadier
Sophie Decrée
Royal Belgian Institute of Natural Sciences (RBINS)
Yara Suomi oy
GeoRessources
Centre National de la Recherche Scientifique (CNRS)-Université de Lorraine (UL)-Centre de recherches sur la géologie des matières premières minérales et énergétiques (CREGU)-Institut national des sciences de l'Univers (INSU - CNRS)
Laboratoire Géochimie, Traçage Isotopique, Minéral et élémentaire - G-Time (Bruxelles, Belgium)
University of Würzburg = Universität Würzburg
University of Mons [Belgium] (UMONS)
ANR-10-LABX-0021,RESSOURCES21,Strategic metal resources of the 21st century(2010)
Source :
Applied Geochemistry, Applied Geochemistry, Elsevier, 2020, 123, pp.104778. ⟨10.1016/j.apgeochem.2020.104778⟩, Applied geochemistry, 123
Publication Year :
2020
Publisher :
HAL CCSD, 2020.

Abstract

The Siilinjärvi phosphate deposit (Finland) is hosted by an Archean carbonatite complex. The main body is composed of glimmerite, carbonatite and combinations thereof. It is surrounded by a well-developed fenitization zone. Almost all the rocks pertaining to the glimmerite-carbonatite series are considered for exploitation of phosphate. New petrological and in-situ geochemical as well as spectroscopic data obtained by cathodoluminescence, Raman and laser-induced breakdown spectroscopy make it possible to constrain the genesis and evolution of apatite through time. Apatite in the glimmerite-carbonatite series formed by igneous processes. An increase in rare earth elements (REE) content during apatite deposition can be explained by re-equilibration of early apatite (via sub-solidus diffusion at the magmatic stage) with a fresh carbonatitic magma enriched in these elements. This late carbonatite emplacement has been known as a major contributor to the overall P and REE endowment of the system and is likely connected to fenitization and alkali-rich fluids. These fluids - enriched in REE - would have interacted with apatite in the fenite, resulting in an increase in REE content through coupled dissolution–reprecipitation processes. Finally, a marked decrease in LREE is observed in apatite hosted by fenite. It highlights the alteration of apatite by a REE-poor fluid during a late-magmatic/hydrothermal stage. Regarding the potential for REE exploitation, geochemical data combined with an estimation of the reserves indicate a sub-economic potential of REE to be exploited as by-products of phosphate mining. Spectroscopic analyses further provide helpful data for exploration, by determining the P and REE distribution and the enrichment in carbonatite and within apatite.<br />SCOPUS: ar.j<br />info:eu-repo/semantics/published

Details

Language :
English
ISSN :
08832927
Database :
OpenAIRE
Journal :
Applied Geochemistry, Applied Geochemistry, Elsevier, 2020, 123, pp.104778. ⟨10.1016/j.apgeochem.2020.104778⟩, Applied geochemistry, 123
Accession number :
edsair.doi.dedup.....367e25e4369c92fba2f82dfc3d575e8a
Full Text :
https://doi.org/10.1016/j.apgeochem.2020.104778⟩