V11C-3076
Kimberlite emplacement record in diamond morphology

Monday, 14 December 2015
Poster Hall (Moscone South)
Yana Fedortchouk, Dalhousie University, Department of Earth Sciences, Halifax, NS, Canada and Ingrid Chinn, DeBeers Exploration, Johannesburg, South Africa
Abstract:
Diamond resorption morphology reflects conditions and events in the host kimberlite magma and in diamond sources in subcratonic mantle. Recent experimental studies on diamond dissolution enable us now to use surface features of diamonds to examine magmatic fluid in kimberlites. This study uses optical and scanning electron microscopy examination of ~750 macro-diamonds from two kimberlites in Orapa cluster, Botswana. Kimberlite A is a simple body filled with coherent kimberlite facies (CK); kimberlite B is a complex body with two facies of coherent kimberlite and a massive volcaniclastic kimberlite facies (MVK). Distinction between kimberlite-induced and mantle-derived resorption was based on: the type of the most abundant resorption style, morphology of crystals with attached kimberlite fragments, and the study of pseudohemimorphic diamonds. Kimberlite-induced resorption is the focus of this work. The three facies in the pipe B show three contrasting diamond resorption types. Resorption in MVK facies leads to glossy rounded surfaces with fine striation and hillocks, and is identical to the resorption style in CK facies of pipe A. This type of resorption is typical for volcaniclastic facies and indicates emplacement in the presence of abundant COH fluid with high H2O:CO2 ratio (>50mol% of H2O). We propose that pipe A is a root zone supplying material to a larger kimberlite body filled with VK. The two CK in pipe B have very different resorption style. One forms similar glossy surfaces but with regular small cavities of rounded outline, while the other seems more corrosive and develops extremely rough features and deep cavities. Comparison to the experimental data suggests that the former had almost pure H2O fluid at low pressure (where solubility of SiO2 is low). The later CK facies was emplaced in the absence or very low abundance of a free fluid, and possibly in melt closer to carbonatitic composition.