Abstract

Rhenium–osmium (Re–Os) isotope and elemental abundances have been obtained for primary mantle minerals, metasomatic phases, and a range of mantle rock types from xenoliths in recent volcanics in northern Tanzania. Re and Os abundances for sulphide and coexisting silicates in garnet lherzolites from Lashaine confirm that sulphide dominates the Os budget, but also show that Re is almost exclusively sited in silicate phases. Silicate minerals from two different samples yield 187Re– 188Os ages of 15.4±6.1 and 31.4±6.3 Myr, respectively. Comparison with 232Th– 208Pb (267.1±4.4 Myr) 147Sm– 143Nd (164±18 Myr) and 87Rb– 87Sr (in equilibrium at the present-day) ages for the same silicate minerals suggests differential closure between these isotope systems, and a closure temperature of ≥670°C for the Re–Os system. Remarkably, sulphide inclusions were not affected by diffusional equilibration between the silicates, and preserve significantly older age information. Model calculations suggest that sulphide–silicate equilibration ceased some 200–300 Ma, and the Os isotope composition of the sulphide ( 187Os/ 188Os=0.10432±0.00013) suggests a minimum age of 3.4 Gyr. Most xenoliths possess Os isotope compositions that are less radiogenic than the present-day chondritic mantle indicating that they experienced Re-loss some time ago. Samples showing evidence for modal metasomatism have high Re concentrations and Re/Os ratios, but their relatively unradiogenic Os isotope compositions suggests that the metasomatism occurred recently, consistent with data for metasomatic vein minerals. In contrast, some dunites possess both high Re/Os ratios and radiogenic Os isotope compositions. These samples differ from those affected by modal metasomatism in having low Re and exceptionally low Os concentrations. These results provide quantitative constraints on the distribution of Re and Os amongst mantle minerals, highlight the potential of Re–Os isotope dating of sulphide inclusions for establishing the early history of mantle mineral assemblages, and demonstrate that mantle processes themselves (metasomatism and dunite formation) can significantly modify the Os isotope chemistry of mantle rocks.

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