Tetrahedrally coordinated boron in tourmalines from the liddicoatite-elbaite series from Madagascar: Structure, chemistry, and infrared spectroscopic studies

Author(s)
Andreas Ertl, John M. Hughes, Stefan Prowatke, Thomas Ludwig, Pinnelli S.R. Prasad, Franz Brandstätter, Wilfried Körner, Ralf Schuster, Franz Pertlik, Horst Marschall
Abstract

Four colorless tourmalines of the liddicoatite-elbaite series from pegmatites from Anjanabonoina, Madagascar, have been characterized by crystal-structure determination and by chemical analyses. Optimized formulae range from X(Ca0.57Na0.29 ?0.14)Y(Al1.141Li1.33 Mn0.072+? 0.19) ZAl6T(Si5.86 B0.14)O18(BO3)3V(OH)3.00W[F0.76 (OH)0.24] [a = 15.8322(3), c = 7.1034(3) Å] to X(Na0.46Ca0.30?0.24) Y(Al1.82Li0.89Fe0.012+Mn0.012+?0.27) ZAl6T(Si5.56 B0.44)O18(BO3)3V(OH)3.00W[(OH)0.50 F0.50] [a = 15.8095(9), c = 7.0941(8) Å] (R = 1.3-1.7%). There is a high negative correlation (r2 = 0.984) between the bond-lengths (?1.618-1.614 Å) and the amount of IVB (from the optimized formulae). Similar to the olenites (from Koralpe, Austria) the liddicoatite-elbaite samples show a positive correlation between the Al occupancy at the Y site and IVB (r2 = 0.988). Short-range order configurations show that the presence of IVB is coupled with the occupancy of (Al2Li) and (Al2?) at the Y site. The structural formulae of the Al-rich tourmalines from Anjanabonoina, Madagascar, show ??0.2 (vacancies) on the Y site. We believe that short-range order configurations with Y(Al2?) are responsible for these vacancies. Hence, an oft-used calculation of the Li content by difference on the Y site may be problematic for Al-rich tourmalines (olenite, elbaite, rossmanite). Fourier transform infrared (FTIR) spectra were recorded from the most IVB-rich tourmaline sample. The bands around 5195 and 5380 cm-1 can be assigned to H2O. Because these bands still could be observed in FTIR spectra at temperatures from -150 to +600 °C, it seems unlikely that they result from H2O in fluid inclusions. Interestingly, another FTIR spectrum from a dravite in which the X site is filled completely with Na, does not show bands at ?5200 and ?5400 cm-1. Although not definitive, the resulting spectra are consistent with small amounts of H2O at the X site of the elbaite. The rare-earth element (REE) pattern of the B-rich elbaite (?REE: ?150 ppm) demonstrates that this sample is strongly enriched in LREEs compared to HREEs and exhibits a negative Eu anomaly. This sample shows the strongest enrichment of LREEs and a high LaN/YbN ratio of ?351, which seems to confirm an important role of the fractional crystallization process.

Organisation(s)
Department of Mineralogy and Crystallography
External organisation(s)
Miami University, Scientific Software Center, National Geophysical Research Institute (NGRI), Naturhistorisches Museum Wien (NHM), Geologische Bundesanstalt
Journal
American Mineralogist: an international journal of earth and planetary materials
Volume
91
Pages
1847-1856
No. of pages
10
ISSN
0003-004X
Publication date
2006
Peer reviewed
Yes
Austrian Fields of Science 2012
105116 Mineralogy, 105904 Environmental research
Portal url
https://ucrisportal.univie.ac.at/en/publications/b2f1dd38-7757-4aef-b0b5-8297e7415ee2