2015 GSA Annual Meeting in Baltimore, Maryland, USA (1-4 November 2015)

Paper No. 131-14
Presentation Time: 9:00 AM-6:30 PM

THE PETROGENESIS AND GEOCHEMISTRY OF THE ZANDKOPSDRIFT CARBONATITE COMPLEX, NAMAQUALAND, SOUTH AFRICA


OGUNGBUYI, P.I., JANNEY, P. E. and HARRIS, C., Department of Geological Sciences, University of Cape Town, Rondebosch, Cape Town, 7701, South Africa, priscyem@gmail.com

Petrologic and geochemical data for carbonatites and associated alkaline igneous rocks are presented for the Zandkopsdrift Carbonatite Complex, Namaqualand. The samples included in this study are relatively fresh, collected by coring at depths of >70 m below the weathered cap zone. The Zandkopsdrift complex is the only locality in the province known to contain significant carbonatite. The carbonatites studied are calico-, ferro- and silico- carbonatites, based on mineralogy, texture, and major element composition. They have low to moderate Mg-numbers (35-65), variable MgO contents (1.2-8.50 wt.%) and high atomic Ca/Ca+Mg (0.73-0.97), indicating that they are not likely simple mantle melts. The carbonatites contain significant apatite, magnetite, pyrochlore and phlogopite. Zandkopsdrift also contains significant amounts of aillikite and olivine melilitite. These rocks have relatively low SiO2 (25-31 wt.%) and Al2O3 (5.3- 6.1 wt.%), high K2O (6-6.3 wt.%) and TiO2 (5.6-9.5 wt.%) and moderate Mg numbers (51-58). δ18O and δ13C isotopes were measured for carbonatites and aillikites. δ13CPDB values are close to those expected for mantle-derived carbonatites (-3.9 to -8.83‰), while the δ18OSMOW values are significantly higher (+13. 25 to 21.84‰). The high δ18O value observed in carbonatites and aillikites is most likely attributable to secondary alteration by hydrous/hydrothermal fluids. This supports the inference that the Zandkopsdrift carbonatite is magmatic in origin but was later affected by secondary alteration which resulted in the elevated O stable isotopes. The ‘mantle-like’ δ13C is inconsistent with significant assimilation of C-bearing crustal rocks. Chondrite-normalised REE contents in the carbonatites are 2400 to 10,600 for La and 36 to 170 for Lu. The high REE contents of the carbonatites are most likely due to a combination of a source metasomatised by a highly LREE-enriched agent, as well as significant magmatic differentiation. The relatively fractionated composition of the Zandkopsdrift aillikites and melilitites is also consistent with this hypothesis. We propose that the Zandkopsdrift carbonatites were most likely formed by either immiscible liquid separation from or fractional crystallization of a moderately fractionated, carbonate-rich silicate parental magma.
Handouts
  • OGUNGBUYI ET AL., GSA 2015 ZANDKOPSDRIFT CARBONATITE.pdf (1.2 MB)