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Analytical procedures for U-Pb isotope dilution analyses at the Pará-Iso isotope geology laboratory of the Federal University of Pará (UFPA) are described in detail. The procedures are applied to zircon, titanite, rutile, apatite, columbite-tantalite and whole rock. Reagent preparation and chemical processing are done in clean-room conditions. Samples are dissolved using Teflon ™ microcapsules in steel jacket Teflon ™ Parr Instrument ™ bomb or Teflon ™ screw cap containers. U and Pb are separated using anion exchange AG 1x8 resin columns. Typical blanks for mineral sample amounts of 0.01 to 1.0 mg are less than 1 pg U and 20-30 pg Pb. Isotope analysis of the U and Pb from the same fi lament are carried out using a Finnigan MAT 262 mass-spectrometer in static and dynamic modes. The current analytical level is demonstrated on analyses of international standard zircon 91500 with three different 235 U-205 Pb and 235 U-208 Pb isotope tracers and whole rock standards. Results of analyses of two zircon samples are also presented.

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We studied the Sm–Nd, Rb–Sr, and Re–Os isotope compositions of mantle xenoliths (eclogites and peridotites) from diamondiferous kimberlites of the Catoca cluster of the Kasai Craton. In the eclogites, the primary strontium isotope composition 87Sr/86Sr varies from 0.7056 to 0.7071, and the neodymium isotope composition εNd, from 1.8 to 2.6. The 187Re/188Os and 187Os/188Os ratios range from 135 to 80 and from 1.3110 to 1.9709, respectively, which indicates a significant portion of radiogenic 187Os: γOs = 129-147. These isotope values exceed the values assumed for model reservoirs (primitive upper mantle (PUM) and bulk silicate Earth (BSE)) and those of chondrites. The isotope composition of the studied systems indicates the formation of eclogites from a rhenium-enriched source, namely, the subducted oceanic crust transformed as a result of metasomatism and/or melting under upper-mantle conditions.