Highly variable content of fluorapatite-hosted CO32−in the Upper Cretaceous/Paleogene phosphorites (Morocco) and implications for paleodepositional conditions

Phosphorus (P) usually occurs as microcrystalline minerals of carbonate fluorapatite (CFA) in sediments of upwelling-related areas. The Upper Cretaceous/Paleogene marine sedimentary rocks in Morocco host the world's largest economic reserves in phosphorus, which were deposited on the eastern pa...

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Veröffentlicht in:Chemical geology 2022-05, Vol.597, Article 120818
Hauptverfasser: Aubineau, Jérémie, Parat, Fleurice, Elghali, Abdellatif, Raji, Otmane, Addou, Aissam, Bonnet, Clément, Muñoz, Manuel, Mauguin, Olivia, Baron, Fabien, Jouti, Moulay Brahim, Yazami, Oussama Khadiri, Bodinier, Jean-Louis
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Sprache:eng
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Zusammenfassung:Phosphorus (P) usually occurs as microcrystalline minerals of carbonate fluorapatite (CFA) in sediments of upwelling-related areas. The Upper Cretaceous/Paleogene marine sedimentary rocks in Morocco host the world's largest economic reserves in phosphorus, which were deposited on the eastern passive margin of the central Atlantic Ocean. However, a full petrographic, mineralogical and geochemical characterization of the Moroccan phosphate minerals is yet to be determined. Here, we use optical and scanning electron microscopies, X-ray diffraction, and infrared spectroscopy, in combination with a microprobe analyzer to document carbonate (CO32−) substitutions in CFA from two distinct phosphate basins and their possible implications for paleoenvironmental conditions. The Moroccan phosphorus-rich deposits predominantly comprise porous phosphatic peloids and coated grains with a maximum size of 500 μm, which in turn consist of high-density nano- to micron-sized rod-shaped and sphere-like crystallites. Bulk and in situ analyses reveal heterogeneous CO32−content in CFA at the regional- and grain-scale. Fourier transform infrared spectra indicate that CO32−accommodates only in the phosphate site within the fluorapatite structure, as found in other natural phosphate minerals. Bulk CO32−variations in CFA between phosphate basins, ranging from 1.97 to 8.24%, are likely related to depositional conditions – and thus of supersaturation with respect to CFA – during mineral formation, transport, and redeposition. Moreover, some phosphatic coated grains have revealed alternations of CO32−-rich and CO32−-poor CFA laminae, pointing out local differences in CO32−concentrations in sediment pore waters. Interestingly, the change in shape and diminution in size of CFA crystallites caused by high content of CFA-hosted CO32−could have possibly increased the intragranular porosity, highlighting an underestimated role of CO32−on grain morphology. Considering the higher solubility of CO32−-rich CFA than fluorapatite, the application of such phosphate rocks from specific Moroccan areas as rock phosphate powders may be of deep interest for long-term soil fertilization. These results further evidence the importance of studying phosphorites for economic, environmental, and scientific interests.
ISSN:0009-2541
1872-6836
DOI:10.1016/j.chemgeo.2022.120818