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Labradorite

From Wikipedia, the free encyclopedia
Feldspar mineral
Labradorite
Labradorite in a polished rock slab
General
CategoryTectosilicateminerals,feldspargroup,plagioclase series
Formula(Ca,Na)(Al,Si)4O8, where Na is 30-50% & Ca is 50–70%
Crystal systemTriclinic
Crystal classPinacoidal (1)
(sameH-M symbol)
Unit cella = 8.155 Å, b = 12.84 Å
c = 10.16 Å; α = 93.5°
β = 116.25°, γ = 89.133°; Z = 6
Identification
ColorGray, gray-white, brown, greenish, pale green, blue, orange, pink, yellow, colorless
Crystal habitCrystals typically thin and tabular, rhombic in cross section, striated; massive
TwinningCommon byalbite,pericline, Carlsbad, Baveno, or Manebach twin laws
CleavagePerfect on {001}, less perfect on {010}, intersecting at near 90°; distinct on {110}
FractureUneven to conchoidal
Mohs scale hardness6–6.5
LusterVitreous to pearly on cleavages
StreakWhite
DiaphaneityTranslucent to transparent
Specific gravity2.68 to 2.72
Optical propertiesBiaxial (+)
Refractive indexnα = 1.554–1.563
nβ = 1.559–1.568
nγ = 1.562–1.573
Birefringenceδ = 0.008–0.010
2V angleMeasured: 85°
DispersionNone
Other characteristicsLabradorescence (iridescence,schiller optical effect)
References[1][2][3]
Labradorite (Spectrolite) – Ylämaa,  Finland.

Labradorite ((Ca,Na)(Al,Si)4O8) is a calcium-enrichedfeldsparmineral first identified inLabrador, Canada, which can display aniridescent effect (schiller).

Labradorite is an intermediate to calcic member of theplagioclase series. It has ananorthite percentage (%An) of between 50 and 70. Thespecific gravity ranges from 2.68 to 2.72. The streak is white, like mostsilicates. Therefractive index ranges from 1.559 to 1.573 andtwinning is common. As with all plagioclase members, the crystal system istriclinic, and three directions ofcleavage are present, two of which are nearly at right angles and are more obvious, being of good to perfect quality (while the third direction is poor). It occurs as clear, white to gray, blocky tolath shaped grains in commonmaficigneous rocks such asbasalt andgabbro, as well as inanorthosites.

Occurrence

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Thegeological type area for labradorite isPaul's Island near the town ofNain in Labrador, Canada. It has also been reported in Poland, Norway, Finland and various other locations worldwide, with notable distribution in Madagascar, China, Australia, Slovakia and the United States.[2]

Labradorite occurs inmafic igneous rocks and is the feldspar variety most common inbasalt andgabbro. The uncommonanorthosite bodies are composed almost entirely of labradorite.[4] It also is found in metamorphicamphibolites and as a detrital component of some sediments. Common mineral associates in igneous rocks includeolivine,pyroxenes,amphiboles andmagnetite.[1]

Labradorescence

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See also:Adularescence
Labradorescence in labradorite
Video of labradorescence in labradorite, visible as the angle of view changes

Labradorite can display aniridescent optical effect (orschiller) known as labradorescence. The termlabradorescence was coined byOve Balthasar Bøggild, who defined it (labradorization) as follows:[5]

Labradorization is the peculiar reflection of the light from submicroscopical planes orientated in one direction (rarely in two directions); these planes have never such a position that they can be expressed by simple indices, and they are not directly visible under the microscope.

Contributions to the understanding of the origin and cause of the effect were made byRobert Strutt, 4th Baron Rayleigh (1923), and by Bøggild (1924).[5][6][7]

The cause of this optical phenomenon is phaseexsolution lamellar structure,[8] occurring in the Bøggildmiscibility gap.[9] The effect is visible when the lamellar separation is between 128 and 252 nm (5.0×10−6 and 9.9×10−6 in); the lamellae are not necessarily parallel;[9] and the lamellar structure is found to lack long range order.[10]

The lamellar separation only occurs in plagioclases of a certain composition; those of calcic labradorite (50–70% anorthite) andbytownite (formula:(Ca0.7-0.9,Na0.3-0.1)[Al(Al,Si)Si2O8],i.e., with ananorthite content of ~70 to 90%) particularly exemplify this.[8][11] Another requirement for the lamellar separation is a very slow cooling of the rock containing the plagioclase. Slow cooling is required to allow the Ca, Na, Si, and Al ions to diffuse through the plagioclase and produce the lamellar separation. Therefore, not all labradorites exhibit labradorescence (they might not have the correct composition, cooled too quickly, or both), and not all plagioclases that exhibit labradorescence are labradorites (they may be bytownite).

Somegemstone varieties of labradorite exhibiting a high degree of labradorescence are calledspectrolite.

Gallery

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  • Polished block from Madagascar
    Polished block from Madagascar
  • Detail of labradorite
    Detail of labradorite
  • Polished labradorite 18 × 20 cm
    Polished labradorite 18 × 20 cm
  • Polished labradorite from UCL Geology collections
    Polished labradorite from UCL Geology collections
  • Labradorite with rare colors
    Labradorite with rare colors
  • Polished labradorite
    Polished labradorite

See also

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References

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  1. ^abHandbook of Mineralogy
  2. ^abMindat.org
  3. ^Webmineral data
  4. ^Hurlbut, Cornelius S.; Klein, Cornelis;Manual of Mineralogy, Wiley, 1985, 20th ed., p. 456,ISBN 0-471-80580-7
  5. ^abBøggild, Ove Balthasar (1924),"On the Labradorization of the Feldspars"(PDF),Kongelige Danske Videnskabernes Selskab, Mathematisk-fysiske Meddelelelser,6 (3):1–79, archived fromthe original(PDF) on April 2, 2015
  6. ^Raman, Chandrasekhara Venkata; Jayaraman, Aiyasami (July 1950)."The structure of labradorite and the origin of its iridescence".Proceedings of the Indian Academy of Sciences, Section A.32 (1):1–16.doi:10.1007/BF03172469.S2CID 128235557.
  7. ^Lord Rayleigh (3 April 1923), "Studies of Iridescent Colour and the Structure Producing it. III. The Colours of Labrador Felspar",Proceedings of the Royal Society of London. Series A,103 (720), The Royal Society:34–45,Bibcode:1923RSPSA.103...34R,doi:10.1098/rspa.1923.0037,JSTOR 94093
  8. ^abYan-ju, Peng; Xue-mei, He; Qin-fang, Fang (May 2008),"Exsolution lamellar structure causes of iridescence in labradorite: evidence from TEM",Acta Petrologica et Mineralogica, archived fromthe original on 2021-11-06, retrieved2015-03-01
  9. ^abHao, Xie; Jing-cheng, Pei; Li-ping, Li (February 2006),"Relation Between Labradorescence and Internal Structure of Labradorite",Geological Science and Technology Information, archived fromthe original on 2021-11-06, retrieved2015-03-01
  10. ^Bolton, Herbert Cairns; Bursill, Leslie Arthur; McLaren, Alexander Clark; Turner, Robin G. (1966). "On the origin of the colour of labradorite".Physica Status Solidi B.18 (1):221–230.Bibcode:1966PSSBR..18..221B.doi:10.1002/pssb.19660180123.S2CID 95485108.
  11. ^MacKenzie, William Scott; Zussman, Jack, eds. (1974), "23. Electron-optical study of a schiller labradorite",The Feldspars: Proceedings of a NATO Advanced Study Institute, Manchester, 11–21 July 1972, vol. 2, Manchester University Press, pp. 478–490

External links

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