New insights into the origin of the Evate apatite-iron oxide-carbonate deposit, Northeastern Mozambique, constrained by mineralogy, textures, thermochronometry, and fluid inclusions

• Published in: Ore geology reviews Vol. 80; pp. 1072 - 1091
• Main Authors: Hurai, Vratislav, Paquette, Jean-Louis, Huraiová, Monika, Slobodník, Marek, Hvožďara, Pavel, Siegfried, Peter, Gajdošová, Michaela, Milovská, Stanislava
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 01.01.2017
• Subjects: Apatite; Carbonatite; East-African orogen; Evate deposit; Fluid inclusions; U-Th-Pb dating; Evate deposit; Apatite; Carbonatite; East-African orogen; U-Th-Pb dating; Fluid inclusions
• ISSN: 0169-1368; 1872-7360
• DOI: 10.1016/j.oregeorev.2016.09.017

The Evate deposit represents the largest resource of apatite in south-east Africa (155 Mt. ore grading 9.3wt.% P2O5) accumulated in up to 100m thick magnetite-carbonate-apatite horizons conformable to the granulitic gneiss of the Monapo Klippe. Baddeleyite and zircon from early iron-oxide (magnetite, geikielite, spinel), apatite- and forsterite-bearing rocks have been dated to 590±6Ma using the LA-ICPMS U-Pb method, whereas monazites from anhydrite-apatite-carbonate rocks show a concordant U-Pb-Th age corresponding to 449±2Ma. Temperatures inferred from calcite-dolomite solvus data and graphite structural ordering span the interval from ≥815 to 276°C. Primary and secondary fluid inclusions in apatite document calciocarbonatite melts associated with early apatite, and CO2-bearing sulfate-chloride brines progressively diluted with low-salinity, probably metoric waters, towards ultimate stages of the deposit formation. The calciocarbonatite melts have initially coexisted with liquid nitrogen and later with sulfate-chloride brines mixed with N2±CO2 gas. Crystallization of spinel around baddeleyite by the mechanism of Ostwald ripening, nucleation of graphite spherules along pyrrhotite-carbonate boundaries, the occurrence of molybdenite, baddeleyite-to-zircon transformation, and high crystallization temperatures inferred from graphite structural ordering and calcite-dolomite thermometry suggest a magmatic origin of the early mineral assemblages. In contrast, microthermometric characteristics of primary aqueous inclusions in the late apatite and the presence of zeolites (thomsonite-Ca, mezolite) is diagnostic of a low-temperature hydrothermal crystallization. Formation of the early magnetite-apatite-forsterite assemblage is thought to be coeval with mafic alkalic intrusions of the Mazerapane Suite superimposed on the granulite facies metamorphism of the Monapo Klippe. The low-temperature, anhydrite-bearing mineralization was associated with the massive circulation of sulfate-rich brines along fractures activated during the Late Cambrian-Ordovician extension. Origin of the sulfate-rich brines may be genetically related either with the magmatic-hydrothermal differentiation, or with the remobilization of crustal evaporites. [Display omitted] •Evate deposit is interpreted as a magmatic deposit overprinted by low-T fluids•High-T minerals originated during Late-Ediacaran post-collisional cooling•Low-T hydrothermal overprint recorded by sulfate-rich brines•Reactivation indicated by Ordovician monazite