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Notes: Abstract Syngenetic diamond inclusions from the Mwadui kimberlite reveal that an unusually fertile section of lithospheric mantle beneath the Central African Craton was sampled. This is shown by a very high ratio of lherzolitic to harzburgitic garnet inclusions (1:2) and low Mg/Fe-ratios in olivine and orthopyroxene. Geothermometry applied to the peridotitic inclusions indicates disequilibrium between non-touching inclusion pairs to be common. Disequilibrium between garnet-olivine and garnet-orthopyroxene pairs suggests successive iron enrichment during diamond formation, e.g. leading to the presence of harzburgitic garnet and lherzolitic olivine in the same diamond. Apart from the dominant peridotitic inclusion suite (88%), rare eclogitic inclusions occur (2%) and a number of uncertain paragenesis. Two diamonds, one with eclogitic garnets with moderate pyroxene solid solution and the other with a single ferro-periclase inclusion, suggest the contribution of a small sub-lithospheric component. The finding of the association Fe-FeO-Fe3O4 in one single diamond indicates diamond formation over a large range of f O2 conditions, possibly along redox fronts. Steep compositional gradients may also be reflected by the joint occurrence of harzburgitic garnet and a SiO2-phase in the same diamond. Alternatively the formation of the SiO2-phase may be due to extreme carbonation of the peridotitic source. Further unusual findings include the exsolution of a silicate phase from magnetite inclusions, (i.e. primary solution of γ-olivine) and an ilmenite inclusion with an eskolaite (Cr2O3) component of 14.5 mol%, the latter together with harzburgitic paragenesis silicate inclusions.

Notes: Abstract Peridotitic inclusions in alluvial diamonds from the Kankan region of Guinea in West Africa are mainly of lherzolitic paragenesis. Nevertheless, extreme Cr2O3 contents (max. 17 wt%) in some of the exclusively lherzolitic garnets document that the diamond source experienced a previous stage of melt extraction in the spinel stability field. This initial depletion was followed by at least two metasomatic stages: (1) enrichment of LREE and Sr and (2) introduction mainly of MREE–HREE and other HFSE (Ti, Y, Zr, Hf). The Ti- and HFSE-poor character of stage (1) points towards a CHO-rich fluid or carbonatitic melt, the high HFSE in stage (2) favour silicate melts as enriching agent. Eclogitic inclusions are derived from a large depth interval ranging from the lithosphere through the asthenosphere into the transition zone. The occurrence of negative Eu anomalies in garnet and clinopyroxene from both lithosphere and transition zone suggests a possible relationship to subducted oceanic crust. Lithospheric eclogitic inclusions are derived from heterogeneous sources, that may broadly be divided into a low-Ca group with LREE depleted trace element patterns and a high-Ca group representing a source with negative LREE–HREE slope that is moderately enriched in incompatible elements relative to primitive mantle. High-Ca inclusions of majoritic paragenesis are significantly more enriched in incompatible elements, such as in Sr and LREE. Calculated whole rock compositions require metasomatic enrichment even if a derivation from MORB is assumed.

Notes: Abstract The Gibeon Kimberlite Province of southern Namibia comprises more than 75 group 1 kimberlite pipes and dykes. From the Gibeon Townsland 1 pipe, 38 upper mantle xenoliths (23 garnet lherzolites and 15 garnet harzburgites) were collected and minerals were analysed by electron microprobe for major elements. Pressures and temperatures of crystallisation for xenoliths with either coarse equant, porphyroclastic and mosaic-porphyroclastic textures were estimated by a number of combinations of geothermometers and geobarometers judged to be reliable and accurate for peridotites by Brey and Köhler (1990): The P-T estimates for equilibrated xenoliths agree within the errors of the methods and plot within the stability field of graphite. The P-T values for coarse equant xenoliths fall close to a geothermal gradient of about 44 mW/m2 within a very restricted pressure range. The porphyroclastic xenoliths yield similar and higher temperatures at similar depths. In these xenoliths Ca in orthopyroxene and Ca in olivine increase towards the rims and are high in the neoblasts indicating a stage of transient heating at depth. The mosaic-porphyroclastic xenolith minerals yield the highest temperatures, are unzoned and indicate internal mineral equilibrium. The depth of origin for the xenoliths from Gibeon Townsland 1 ranges from 100 to 140 km. The “cold”, coarse equant peridotites are relatively enriched garnet lherzolites with comparatively (to the “hot” peridotites) low modal orthopyroxene contents, whereas the “hot”, mosaic-porphyroclastic peridotites are depleted garnet harzburgites with high modal amounts of orthopyroxene. This is opposite to the findings for peridotites from the Kaapvaal craton where the cold peridotites are depleted harzburgites with high modal orthopyroxene and many of the hot peridotites are fertile lherzolites with low modal abundance of orthopyroxene. We present a model in which the high temperature, depleted garnet harzburgites are equated to the cold, coarse equant peridotites from the Kaapvaal craton. It is envisaged that this material was detached and transported laterally by an upwelling, deflected plume.

Notes: Abstract Frequent inclusions of ferropericlase, some coexisting with phases of MgSiO3, CaSiO3 and SiO2 composition, suggest that a large proportion of diamonds from Guinea are derived from the lower mantle. Low aluminium contents in MgSiO3 inclusions indicate derivation from the uppermost lower mantle, where Al solubility in perovskite is low. Trace element analyses (SIMS) of CaSiO3 inclusions reveal extreme degrees of LREE (200–2000 times chondritic) and Sr enrichment (70–1000 times chondritic) together with negative and positive Eu anomalies. This implies a highly enriched lower mantle source, possibly a product of a subducted oceanic slab. A number of phases that are only stable in the upper mantle are found to coexist with lower mantle phases and thereby indicate retrograde equilibration during slow exhumation within a rising plume or convection cell. In one case, however, an inclusion paragenesis of ferropericlase and olivine can be shown to have formed within the upper mantle, indicating that the occurrence of ferropericlase inclusions alone is an unreliable indicator of lower mantle origin.

Notes: Abstract The positions of the liquidi and the near-liquidus phases of olivine-melilitite+CO2 have been determined under MH-buffered and ‘furnace-buffered’ conditions up to 40 kb. It is found that CO2 alone lowers the liquidus compared to ‘dry’ conditions, yet its influence is minor compared to H2O. The major role of CO2 is to favour the growth of orthopyroxene and garnet over that of olivine at least at high pressures. CO2-contents of glasses from experiments just above the liquidus (MH-buffered) were determined as 5.1 % at 10kb; 7.5 % at 20kb, 9.3 % at 30kb and 10–11 % (estimated) at 40 kb. Experiments on (pyrolite −40 % olivine)+H2O+CO2 show that CO2 occurs under mantle conditions as carbonate under subsolidus conditions and dissolved in a melt above the solidus. At 30kb, the solidus lies between 1,000 ° C and 1,050 ° C for vapour-saturated conditions, at $$X_{{\text{H}}_{\text{2}} {\text{O}}} = 0.5 = X_{{\text{CO}}_{\text{2}} } $$ and at $$X_{{\text{H}}_{\text{2}} {\text{O}}} = 0.9,{\text{ }}X_{{\text{CO}}_{\text{2}} } = 0.1$$ .