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A (1:1) 7-Å Fe Phase and its Transformation in Recent Sediments: An HRTEM and AEM Study

Published online by Cambridge University Press:  28 February 2024

Marc Amouric
Affiliation:
Centre de Recherche sur les Mécanismes de la Croissance Cristalline CRMC2-CNRS, Campus de Luminy, case 913, 13288 Marseille Cedex 9, France
Claude Parron
Affiliation:
Laboratoire de Géosciences de l'Environnement-URA CNRS 132, Université d'Aix-Marseille III, 13397 Marseille Cedex 20, France
Lionel Casalini
Affiliation:
Laboratoire de Géosciences de l'Environnement-URA CNRS 132, Université d'Aix-Marseille III, 13397 Marseille Cedex 20, France
Pierre Giresse
Affiliation:
Laboratoire de Sédimentologie Marine, Université de Perpignan, Av. de Villeneuve, 66025 Perpignan, France
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Abstract

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Young marine green grains, from Fe-rich sediments, were studied by using HRTEM systematically combined with punctual microchemical EDX analyses. Experimental results demonstrated these grains were made of a mixture of very small phases (mainly 1:1 and 2:1 silicates layer phases) with a dominant 7-Å Fe specie. All the main crystallochemically characterized phases appeared intimately related in the same evolutionary process. Each of them experienced different and well described conversion mechanisms. So first, a starting original Fe-rich kaolinite recrystallized via solution into another particular 7-Å Fe-rich phase, the composition of which varies from a di-tri to a pure trioctahedral (Mg + Fe) end member.

This Fe-rich 1:1 mineral is effectively not a classical one. Then crystallization of a 10Å, rather dioctahedral K-rich phase occurs at the expense of it, through 1:½:1 interstratified structures. Such an evolution takes place through a solid state mechanism in which one 10-Å layer replaces one 7-Å layer. Another part of mica-like structures may also directly develop after dissolution of original kaolinites. The development of 10-Å K-rich phases could be significative of the beginning of the glauconitization process in these grains.

Type
Research Article
Copyright
Copyright © 1995, The Clay Minerals Society

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