The geochemistry and petrogenesis of the Saltpeterkop carbonatite complex near Sutherland, Northern Cape, South Africa

Master Thesis

2018

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University of Cape Town

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The Saltpeterkop Carbonatite Complex is a Late Cretaceous (≈76 Ma) volcanic and shallow intrusive magmatic feature located approximately 20 km southeast of Sutherland in the Northern Cape. It is unusual among southern African carbonatite complexes in that it has not been deeply eroded, and retains a significant vestige of its original volcanic features. The main geologic expression of the Complex is a ≈1.5 km diameter tuff ring, located on top of prominently updomed and fractured Beaufort Group (Karoo) sediments, that appears to have formed as the result of a major diatreme-type eruption. The volcaniclastic breccias making up the tuff ring have been heavily altered and silicified by hydrothermal activity, and thick (mm to tens of cm) Fe oxide-rich crusts, which appear to represent the alteration products of Fe-rich carbonatites, are common in this area. Outside of the central ring structure are numerous shallow intrusions (dykes, sills and irregular shapes), satellite breccia pipes and pipe-shaped intrusions that host fresh to only moderately altered igneous rocks. The main igneous rock types include (in decreasing order of abundance): carbonatite, potassic trachyte, olivine melilitite and ultramafic lamprophyre. This thesis provides the first detailed petrographic and geochemical description of these rocks (e.g., major and trace elements) and attempts to explain several aspects of their petrogenesis. The olivine melilitites and ultramafic lamprophyres are the most primitive igneous rocks in the complex and have experienced only minor to moderate extents of differentiation, respectively. They apppear to have been derived by low-degrees of partial melting of a carbonated, likely phlogopite-bearing mantle source. The lamprophyres appear to have been derived by melting at shallower depths than the melilitites based on REE constraints. The carbonatites range from relatively primitive to highly differentiated and they form a nearly continuous compositional range with the ultramafic lamprophyres and melilitites. This seems to argue against a major role for liquid immiscibility in their origin. Their REE content (up to 2 wt.% total REE oxides) correlates with their extent of differentiation. The potassic trachytes are plausibly linked to melts of mafic lower continental crust that has been metasomatised by hydrous potassium-rich carbonatitic melts and which have experienced significant fractional crystallization and assimilation of upper crustal sedimentary rocks during emplacement.
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