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

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 con...

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Bibliographic Details
Main Authors: Decrée, Sophie, Savolainen, Mikko, Mercadier, Julien, Debaille, Vinciane, Höhn, Stefan, Frimmel, Hartwig H.E.E., Baele, Jean-Marc
Format: Article in Journal/Newspaper
Language:English
Published: 2020
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Online Access:http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/313656
https://dipot.ulb.ac.be/dspace/bitstream/2013/313656/3/Decreeetal2020.pdf
Description
Summary: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. SCOPUS: ar.j info:eu-repo/semantics/published