Bebedourite from its type area (Salitre I complex): A key petrogenetic series in the Late-Cretaceous Alto Paranaiba kamafugite-carbonatite-phoscorite association, Central Brazil

Rocha Barbosa, Elisa Soares; Brod, Jose Affonso; Junqueira-Brod, Tereza Cristina; Dantas, Elton Luiz; de Oliveira Cordeiro, Pedro Filipe; Gomide, Caroline Siqueira

Abstract

Bebedourite is a cumulate rock composed of variable but roughly equant amounts of diopside, apatite, magnetite, phlogopite, and a Ca-Ti phase (mostly perovskite, more rarely titanite and/or Ti-garnet). Other minerals may be modally important, such as olivine and K-feldspar in the least and most evolved members of the bebedourite series, respectively. The magmatic evolution in bebedourites is accompanied by a progressive increase in SiO2 activity, which results in the transformation of perovskite into titanite and titanite into Ti-gamet. Although the SiO2 increase may, in some cases, result from crustal contamination, it seems to be a localized effect and cannot account for the evolution of the whole bebedourite series. Crystal fractionation is supported by the chemical variation of key mineral phases such as pyroxene and phlogopite. The Salitre complex is an ultrapotassic carbonatite- and phoscorite-bearing plutonic complex belonging to the Late-Cretaceous Alto Paranaiba Igneous Province (APIP) and consisting of three main bodies (Salitre I, II, and III). The complex is composed mainly of bebedourite, with lesser amounts of carbonatite and phoscorite in its central-north portion. A particular type of bebedourite, where the main Ca-Ti phase is Ti-garnet, dominates the southern part of Salitre land also occurs as dikes crosscutting older bebedourites, suggesting that Ti-gamet-bebedourites form an independent intrusion. Sr and Nd isotopic data indicate that the parental magmas to the bebedourites in the Salitre complex originated in a metasomatized sub-continental lithospheric mantle similar to that involved in the origin of the rest of the APIP. (C) 2012 Elsevier B.V. All rights reserved.

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Título según WOS: ID WOS:000306155100005 Not found in local WOS DB
Título de la Revista: LITHOS
Volumen: 144
Editorial: A.C. Kerr Cardiff University, Cardiff, UK X.-H. Li Chinese Academy of Sciences (CAS), Beijing, China M. Roden University of Georgia, Athens, Georgia, USA M. Scambelluri Universita ` degli Studi di Genova, Genova, Italy
Fecha de publicación: 2012
Página de inicio: 56
Página final: 72
DOI:

10.1016/j.lithos.2012.04.013

Notas: ISI