Anorthoclase
Anorthoclase | |
---|---|
General | |
Category | Feldspar |
Formula (repeating unit) | (Na,K)AlSi3O8 |
IMA symbol | Ano[1] |
Strunz classification | 9.FA.30 |
Crystal system | Triclinic |
Crystal class | Pinacoidal (1) (same H–M symbol) |
Space group | C1 |
Unit cell | a = 8.28, b = 12.97 c = 7.15 [Å]; α = 91.05° β = 116.26°, γ = 90.15°; Z = 4 |
Identification | |
Color | Colorless, also white, pale creamy yellow, red, green |
Crystal habit | Short prismatic crystals; tabular, rhombic, flattened along [010] |
Twinning | Polysynthetic twinning produces a grid pattern on [100] |
Cleavage | Perfect on [001], other partings |
Fracture | Uneven |
Tenacity | Brittle |
Mohs scale hardness | 6 |
Luster | Vitreous to pearly on cleavage planes |
Streak | White |
Diaphaneity | Transparent |
Specific gravity | 2.57–2.60 |
Optical properties | Biaxial (−) |
Refractive index | nα = 1.519–1.529 nβ = 1.524–1.534 nγ = 1.527–1.536 |
Birefringence | δ = 0.008 |
2V angle | Measured: 34°–60° |
References | [2][3][4] |
The mineral anorthoclase ((Na,K)AlSi3O8) is a crystalline solid solution in the alkali feldspar series, in which the sodium-aluminium silicate member exists in larger proportion. It typically consists of between 10 and 36 percent of KAlSi3O8 and between 64 and 90 percent of NaAlSi3O8.[5]
Structure and stability
[edit]Anorthoclase is an intermediate member of the high albite – sanidine alkali feldspar solid solution series. Intermediate members of this series, high albite, anorthoclase and high sodium sanidine are stable at temperatures of 600 °C (1,100 °F) and above. Below 400–600 °C (800–1,100 °F) only very limited solution exists (less than about 5% on both the low albite and microcline ends).[6] Anorthoclase and high albite exhibit triclinic symmetry, whereas sanidine and the low temperature orthoclase have monoclinic symmetry.[6] If the high temperature intermediate composition alkali feldspars are allowed to cool slowly, exsolution occurs and a perthite structure results.[6]
Occurrence
[edit]Anorthoclase occurs in high temperature sodium rich volcanic and hypabyssal (shallow intrusive) rocks. The mineral is typically found as a constituent of the fine grained matrix or as small phenocrysts which may occur as loose crystals in a weathered rock.[2]
It was first described in 1885 for an occurrence on Pantelleria Island, Trapani Province, Sicily. The name is from the Greek αν-, ορθός and κλάσις (not cleaving at right-angles), for its oblique cleavage.[2][3]
See also
[edit]References
[edit]- ^ Warr, L.N. (2021). "IMA–CNMNC approved mineral symbols". Mineralogical Magazine. 85 (3): 291–320. Bibcode:2021MinM...85..291W. doi:10.1180/mgm.2021.43. S2CID 235729616.
- ^ a b c "Handbook of Mineralogy" (PDF). Archived from the original (PDF) on 2016-03-04. Retrieved 2011-12-04.
- ^ a b "Mindat.org".
- ^ "Webmineral data".
- ^ Deere; Howie; Zussman. Framework Silicates. Rock Forming Minerals. Vol. 4. Wiley. pp. 2–5, Fig. 1.
- ^ a b c Klein, Cornelis; Hurlbut, Cornelius S. Jr. Handbook of Mineralogy. Wiley. pp. 446–449, Fig. 11-95. ISBN 0-471-80580-7.