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1 Institute of Geological Sciences, Masaryk University, Kotlá
ská 2,611 37 Brno, Czech Republic
2 Institute of Geochemistry, Mineralogy and Mineral Resources, Charles University, Albertov 6, 128 43 Praha, Czech Republic
3 Department of Geological Sciences, University of Manitoba, Winnipeg R3T 2N2, Canada
* E-mail: mnovak{at}sci.muni.cz
** Present address: Precambrian Geoscience Section, Ontario Geological Survey, 933 Ramsey Lake Road, Sudbury, Ontario, Canada P3E 6B5.
Wet-chemical analyses (41) of tourmaline from granitic pegmatites (barren, barren-pocket, beryl, lepidolite types) in the Moldanubicum, Czech Republic revealed that members of the oxy-subgroup - common oxy-schorl, minor oxy-dravite and rare oxy-foitite are more abundant relative to the relevant members of the hydroxy-subgroup. The primary substitution mechanisms in tourmaline show combination of heterovalent substitutions: YAlWO YR2+1W(OH)1, X
YAl2 WO XNa1 YR2+2 W(OH)1, X
YAl XNa1 YR2+1 and X
W(OH) XNa1 WO1, and homovalent substitutions: Fe2+Mg1 and (OH)F1. Tourmalines with the chemistry expressed by the general formula X(Na0.5
0.5)Y(R2+2Al)ZAl6(BO3)3Si6O18 V(OH)3 W(O0.5OH0.5) crystallized in very similar PT conditions in granitic systems saturated on Na, Al, Si and H2O, it indicates the importance of short-range order requirements on tourmaline chemical composition. Abundance of heterovalent substitutions involving the W-site requires determination of light elements (H, B, F, Li) and Fe2+/Fe3+ in tourmalines to specify substitution mechanisms with certainty. Normalization of electron-microprobe data of (Fe, Mg)-rich, (Ca, Li, F)-poor tourmalines from granitic pegmatites on (OH, F)3.5O0.5, which is more probable than (OH, F)4, seems to be suitable.
Key-words: tourmaline, schorl, oxy-schorl, dravite, oxy-dravite, oxy-foitite, wet-chemical analyses, substitution mechanisms, granitic pegmatites, Moldanubicum, Czech Republic.
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