4.3 Article

Physical properties and crystal structure of near end-member oxy-dravite from the Beluga occurrence, Nunavut territory, Canada

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MINERALOGICAL MAGAZINE
卷 -, 期 -, 页码 -

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CAMBRIDGE UNIV PRESS
DOI: 10.1180/mgm.2023.59

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oxy-dravite; tourmaline; crystal structure; electron microprobe; LA-ICP-MS; Al-Mg disorder; Raman spectroscopy

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A rare oxy-dravite mineral was found in the Beluga occurrence in Nunavut territory, Canada. It occurs in a calc-silicate rock and commonly forms solid solutions with other minerals. The presence of oxy-dravite is related to metamorphism in the rock.
Oxy-dravite, ideally Na(Al2Mg)(Al5Mg)(Si6O18)(BO3)3(OH)3(O), was found in a composition near its ideal end-member at the Beluga occurrence, Nunavut territory, Canada. It occurs in retrograde albite-muscovite-corundum-calcite domains in a calc-silicate rock. This uncommon oxy-dravite occurs as dark brown, equant to short-prismatic, idiomorphic crystals with vitreous lustre and up to ca. 4 x 3 cm in size. The oxy-dravite is optically uniaxial (-), with omega = 1.6453(5) and e = 1.6074(18); its calculated density is 3.069 g.cm-3 with a compatibility index of 0.016. The Beluga oxy-dravite has trigonal symmetry, space group R3m with a = 15.9121(2) angstrom, c = 7.1788(10) angstrom, V = 1574.12(5) angstrom 3 and Z = 3. The crystal structure was refined to R1 = 1.45 using 1613 unique reflections. The empirical crystal-chemical formula is X(Na0.88Ca0.080.03K0.01)Y(Al1.49Mg1.31Fe0.15Ti0.04Zn0.01)Z(Al5.42Mg0.58)T(Si5.84Al0.16O18)B(BO3)3V(OH2.95O0.05)W(O0.84OH0.01F0.15).Oxy-dravite in nature commonly occurs in a solid solution with foitite, schorl and oxy-schorl. At the Beluga occurrence, its minor contents of Al, vacancy [], and Ca are most likely compensated by (Al)(NaR2+)-1 and (CaMg)(NaAl)-1 exchanges of the oxy-magnesio-foitite and magnesio-lucchesiite components. The Beluga occurrence of oxy-dravite is characterised by an Mg-rich environment related to a metamorphic overprint of the original sedimentary sequence. This sequence of marine dolomitic argillaceous marl was influenced by (B,Cl)-rich fluids, probably proximally-derived from mineral breakdown reactions in the calc-silicate during the retrograde stage of metamorphism. The locality is a rare example of a tourmaline + corundum assemblage.

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