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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creator | 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 |
description | 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. |
doi_str_mv | 10.1016/j.chemgeo.2022.120818 |
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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.</description><identifier>ISSN: 0009-2541</identifier><identifier>EISSN: 1872-6836</identifier><identifier>DOI: 10.1016/j.chemgeo.2022.120818</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>Carbonate fluorapatite ; CO32−substitutions ; Environmental Sciences ; Morocco ; Paleoenvironments ; Porosity</subject><ispartof>Chemical geology, 2022-05, Vol.597, Article 120818</ispartof><rights>2022 Elsevier B.V.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0002-5482-3497 ; 0000-0003-3879-1488 ; 0000-0002-7847-6207 ; 0000-0002-6171-7385</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.chemgeo.2022.120818$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,778,782,883,3539,27907,27908,45978</link.rule.ids><backlink>$$Uhttps://hal.science/hal-03822812$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Aubineau, Jérémie</creatorcontrib><creatorcontrib>Parat, Fleurice</creatorcontrib><creatorcontrib>Elghali, Abdellatif</creatorcontrib><creatorcontrib>Raji, Otmane</creatorcontrib><creatorcontrib>Addou, Aissam</creatorcontrib><creatorcontrib>Bonnet, Clément</creatorcontrib><creatorcontrib>Muñoz, Manuel</creatorcontrib><creatorcontrib>Mauguin, Olivia</creatorcontrib><creatorcontrib>Baron, Fabien</creatorcontrib><creatorcontrib>Jouti, Moulay Brahim</creatorcontrib><creatorcontrib>Yazami, Oussama Khadiri</creatorcontrib><creatorcontrib>Bodinier, Jean-Louis</creatorcontrib><title>Highly variable content of fluorapatite-hosted CO32−in the Upper Cretaceous/Paleogene phosphorites (Morocco) and implications for paleodepositional conditions</title><title>Chemical geology</title><description>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.</description><subject>Carbonate fluorapatite</subject><subject>CO32−substitutions</subject><subject>Environmental Sciences</subject><subject>Morocco</subject><subject>Paleoenvironments</subject><subject>Porosity</subject><issn>0009-2541</issn><issn>1872-6836</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNotUUtOwzAUtBBIlMIRkLyki7T-xK2zQlUFFKmoLMracuyXxlUaR3ZaiRuw5gScjZOQ0C6e3nujmdFIg9A9JWNK6HSyG5sS9lvwY0YYG1NGJJUXaEDljCVTyaeXaEAIyRImUnqNbmLcdS_lQgzQz9Jty-oTH3VwOq8AG1-3ULfYF7ioDj7oRreuhaT0sQWLF2vOfr--XY3bEvBH00DAiwCtNuAPcfKuK_BbqAE3naCb0GkjfnjzwRvjR1jXFrt9UznT2fo64sIH3PQqC42Prgd11aew_3e8RVeFriLcnfcQbZ6fNotlslq_vC7mqwQyQpOpAEOZ0LOCQqpFWmQp4TNKJLNslheiEFIykDmQTBKdQZ5zwlNubWqFSLngQzQ62Za6Uk1wex0-lddOLecr1WOES8YkZUfacR9PXOjyHB0EFY2D2oB1AUyrrHeKEtV3o3bq3I3qu1GnbvgfqYyJUQ</recordid><startdate>20220520</startdate><enddate>20220520</enddate><creator>Aubineau, Jérémie</creator><creator>Parat, Fleurice</creator><creator>Elghali, Abdellatif</creator><creator>Raji, Otmane</creator><creator>Addou, Aissam</creator><creator>Bonnet, Clément</creator><creator>Muñoz, Manuel</creator><creator>Mauguin, Olivia</creator><creator>Baron, Fabien</creator><creator>Jouti, Moulay Brahim</creator><creator>Yazami, Oussama Khadiri</creator><creator>Bodinier, Jean-Louis</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0002-5482-3497</orcidid><orcidid>https://orcid.org/0000-0003-3879-1488</orcidid><orcidid>https://orcid.org/0000-0002-7847-6207</orcidid><orcidid>https://orcid.org/0000-0002-6171-7385</orcidid></search><sort><creationdate>20220520</creationdate><title>Highly variable content of fluorapatite-hosted CO32−in the Upper Cretaceous/Paleogene phosphorites (Morocco) and implications for paleodepositional conditions</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-e901-65ec125a7f1e4a54f940371082d27bf5f5882e8be0980a9ebb30343dd4d554353</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Carbonate fluorapatite</topic><topic>CO32−substitutions</topic><topic>Environmental Sciences</topic><topic>Morocco</topic><topic>Paleoenvironments</topic><topic>Porosity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aubineau, Jérémie</creatorcontrib><creatorcontrib>Parat, Fleurice</creatorcontrib><creatorcontrib>Elghali, Abdellatif</creatorcontrib><creatorcontrib>Raji, Otmane</creatorcontrib><creatorcontrib>Addou, Aissam</creatorcontrib><creatorcontrib>Bonnet, Clément</creatorcontrib><creatorcontrib>Muñoz, Manuel</creatorcontrib><creatorcontrib>Mauguin, Olivia</creatorcontrib><creatorcontrib>Baron, Fabien</creatorcontrib><creatorcontrib>Jouti, Moulay Brahim</creatorcontrib><creatorcontrib>Yazami, Oussama Khadiri</creatorcontrib><creatorcontrib>Bodinier, Jean-Louis</creatorcontrib><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Chemical geology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aubineau, Jérémie</au><au>Parat, Fleurice</au><au>Elghali, Abdellatif</au><au>Raji, Otmane</au><au>Addou, Aissam</au><au>Bonnet, Clément</au><au>Muñoz, Manuel</au><au>Mauguin, Olivia</au><au>Baron, Fabien</au><au>Jouti, Moulay Brahim</au><au>Yazami, Oussama Khadiri</au><au>Bodinier, Jean-Louis</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Highly variable content of fluorapatite-hosted CO32−in the Upper Cretaceous/Paleogene phosphorites (Morocco) and implications for paleodepositional conditions</atitle><jtitle>Chemical geology</jtitle><date>2022-05-20</date><risdate>2022</risdate><volume>597</volume><artnum>120818</artnum><issn>0009-2541</issn><eissn>1872-6836</eissn><abstract>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.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.chemgeo.2022.120818</doi><orcidid>https://orcid.org/0000-0002-5482-3497</orcidid><orcidid>https://orcid.org/0000-0003-3879-1488</orcidid><orcidid>https://orcid.org/0000-0002-7847-6207</orcidid><orcidid>https://orcid.org/0000-0002-6171-7385</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Carbonate fluorapatite CO32−substitutions Environmental Sciences Morocco Paleoenvironments Porosity |
title | Highly variable content of fluorapatite-hosted CO32−in the Upper Cretaceous/Paleogene phosphorites (Morocco) and implications for paleodepositional conditions |
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