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Stable isotope compositions of tourmalines from granites and related hydrothermal rocks of the Karagwe-Ankolean belt,northwest Tanzania
Institution:1. Centre for Wireless Communications (CWC), University of Oulu, P.O. Box 4500, FI-90014, Finland;2. São Paulo State University, Avenida Doutor Octávio da Silva Bastos, 2439, Bairro Jardim Nova São João 13874–149— São João da Boa Vista-SP, Brazil;1. Department of Geology and Paleontology, Faculty of Natural Sciences, Comenius University, Ilkovi?ova 6, SK-842 15 Bratislava, Slovakia;2. Department of Mineralogy and Petrology, Faculty of Natural Sciences, Comenius University, Ilkovi?ova 6, SK-842 15 Bratislava, Slovakia;3. Earth Science Institute, Slovak Academy of Sciences, Dúbravská cesta 9, SK-845 28 Bratislava, Slovakia;4. Earth Science Institute, Slovak Academy of Sciences, Workplace Banská Bystrica, ?umbierska 1, SK-974 01 Banská Bystrica, Slovakia
Abstract:Tourmaline is a ubiquitous mineral in the Mid-Proterozoic, peraluminous, syn- to post-tectonic granites and aplites and the related hydrothermal rocks of the Karagwe-Ankolean belt in northwest Tanzania. Electron microprobe analysis indicates that tourmalines from all of the intrusive and hydrothermal lithologies: (1) belong to the schorl-dravite solid-solution series; and (2) plot within the field occupied by tourmaline from Li-poor granitoids on the Fe-Al-Mg classification diagram. Oxygen isotope compositions range from +12.2 to +11.6‰ (SMOW) for magmatic tourmalines and from +10.8 to +9.8‰ for those of hydrothermal origin. Hydrogen isotope compositions vary from ?79 to ? 65‰ (SMOW) for magmatic tourmalines and from ?99 to ?84‰ for hydrothermal tourmalines. Water contents measured by manometry are constant at 3.0–3.2 wt.%. Within the broad grouping there arc systematic variations in both chemical particularly Fetot/(Fetot + Mg ratio)] and isotopic composition that relate to evolving magmatic and hydrothermal conditions. Igneous differentiation increasing Fetot/(Fetot + Mg) in magmatic tourmaline] has produced trends with higher δ18O in quartz, lower δ18O in tourmaline, and larger ΔQTZ.?TOUR.-values, that reflect a combination of a reduction of crystallization temperature and an increase of Fetot/ (Fetot + Mg) in the residual melt. Subsequent cooling and interaction of an exsolved, B-rich magmatic fluid with the pelitic country rocks, resulted in the deposition of hydrothermal tourmaline with increasing Fetot/(Fetot + Mg) ratios, and progressively lower δ18O and δD -values.
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