Abstract

The 2 Ga-old Ihouhaouene alkaline complex (Western Hoggar, Algeria) is among the oldest known carbonatite occurrences on Earth. The carbonatites are calciocarbonatites hosted by syenites, the predominant rock type in the complex. Both rock types are characterized by medium-grained to pegmatitic textures and contain clinopyroxene, apatite, and wollastonite, associated with K-feldspar in syenites and a groundmass of calcite in carbonatites. The rock suite shows a continuous range of compositions from 57–65 wt.% SiO2and 0.1–0.4 wt.% CO2in red syenites to 52–58 wt.% SiO2and 0.1–6.5 wt.% CO2in white syenites, 20–35 wt.% SiO2and 11–24 wt.% CO2in Si-rich carbonatites (>10% silicate minerals), and <20 wt.% SiO2and 24–36 wt.% CO2in Si-poor carbonatites (<5% silicate minerals). Calculation of mineral equilibrium melts reveals that apatite and clinopyroxene are in disequilibrium with each other and were most likely crystallized from different parental magmas before being assembled in the studied rocks. They are subtle in the red syenites, whereas the white syenites and the Si-rich carbonatites bear evidence for parental magmas of highly contrasted compositions. Apatite was equilibrated with LREE-enriched (Ce/Lu = 1,690–6,182) carbonate melts, also characterized by elevated Nb/Ta ratio (>50), whereas clinopyroxene was precipitated from silicate liquids characterized by lower LREE/HREE (Ce/Lu = 49–234) and variable Nb/Ta ratios (Nb/Ta = 2–30). The Si-poor carbonatites resemble the Si-rich carbonatites and the white syenites with elevated REE contents in apatite equilibrium melts compared to clinopyroxene. However, apatite equilibrium melt in Si-poor carbonatite shows a majority of subchondritic values (Nb/Ta<10) and clinopyroxene has chondritic-to-superchondritic values (Nb/Ta = 15–50). Although paradoxical at first sight, this Nb-Ta signature may simply reflect the segregation of the carbonatite from highly evolved silicate melts characterized by extremely low Nb/Ta values. Altogether, our results suggest an evolutionary scheme whereby slow cooling of a silico-carbonated mantle melt resulted in the segregation of both cumulus minerals and immiscible silicate and carbonate melt fractions, resulting in the overall differentiation of the complex. This process was however counterbalanced by intermingling of partially crystallized melt fractions, which resulted in the formation of hybrid alkaline cumulates composed of disequilibrium cumulus phases and variable proportions of carbonate or K-feldspar.

Highlights

  • Petrological and geochemical studies supported by experimental works have suggested the origin of carbonatites via two main processes: 1) Partial melting of carbonate-rich mantle producing primary carbonate melts (Gittins and Harmer, 1997; Gudfinnsson and Presnall, 2005; Stoppa et al, 2005; Dasgupta and Hirschmann, 2006)

  • Whatever process is envisioned for the origin of carbonatites, the common association of carbonatites with alkaline silicate rocks must be taken into account as it is key stone to the understanding of their petrogenesis

  • The extreme diversity of trace element compositions recorded by the Ihouhaouene equilibrium melts might suggest that the complex was formed from a range of primary mantle melts generated by variable degrees of melting of a carbonated mantle source

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Summary

Introduction

Petrological and geochemical studies supported by experimental works have suggested the origin of carbonatites via two main processes: 1) Partial melting of carbonate-rich mantle producing primary carbonate melts (Gittins and Harmer, 1997; Gudfinnsson and Presnall, 2005; Stoppa et al, 2005; Dasgupta and Hirschmann, 2006). The association of carbonatites with silica-saturated rocks is less common; it was estimated to represent 8% of carbonatites worldwide by Woolley and Kjarsgaard (2008)

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