Athabascaite

Athabascaite
General
Category Selenide mineral
Formula
(repeating unit)
Cu5Se4
Strunz classification 2.BA.15d
Crystal system Orthorhombic
Unknown space group
Unit cell a = 8.227 Å, b = 11.982 Å
c = 6.441 Å; Z = 4
Identification
Color Light grey, bluish-gray to white
Crystal habit As anhedral inclusions and lath shaped crystals, also massive
Mohs scale hardness 2.5
Luster Metallic
Specific gravity 6.59 (calculated)
Optical properties Anisotropism strong, creamy white to dark blue
Pleochroism Distinct, pale gray to blue-gray
References [1][2][3]

Athabascaite is a member of the copper selenide minerals, and forms with other copper selenides. It was first discovered by S. Kaiman in 1949 while he was researching radioactive materials around Lake Athabasca. Kaiman was conducting research near Uranium City, Saskatchewan where mass amounts of uranium mines were present.[4]

History

Kaiman sent his specimens for testing to J. W. Earley, then a graduate student. With the invention of the microprobe analyzer, D.C. Harris decided to delve further into the virtually unknown mineral with little success.[5]

Structure

Because of inavailability of sufficiently large single crystals, little is known about the atomic structure of athabascaite. Copper (Cu+) serves as the cations, selenium (Se2−) serves as the anions, and the two are joined by ionic bonds. The crystal symmetry appears orthorhombic with the lattice parameters a = 8.227 ± 0.01, b = 11.982 ± 0.02, and c = 6.441 ± 0.01 Å. It has a calculated density of 6.59 g/cm3; this density is identical to that of umangite, and therefore the two are thought to have similar structure.[4]

Physical properties

Athabascaite often contains umangite as inclusions and stained carbonate vein material as stringers and veinlets. When coupled with umangite, the mineral forms lath-shaped slender and elongated grains averaging 20 by 50 micrometers. Athabascaite originally appeared as finer grained than the surrounding material, possessing a core of umangite. Because of the presence of umangite within the core, it is thought that the umangite may recrystallize during the construction of athabascaite. Within the hematite, stained carbonate veins contain massive areas up to 300 micrometers in diameter. The veinlets are composed of a collection of arbitrarily organized crystals which rarely surpass 2 micrometres. These crystallites contain pure athabascaite phase.[4]

The color of athabascaite is typically light gray, but can also be white, white-gray, and blue-gray. It has a hardness of approximately 2.50 on the Mohs scale. When exposed to polarized light, it displays a range of colors varying from creamy white to dark blue. The display of these distinct colors, along with its reflectivity, allows athabascaite to be easily distinguished from other copper selenide minerals. It displays strong anisotropy and distinct birefringence.[6]

Geologic occurrence

After being discovered in Canada, a few other samples have been found in Petrovice, Vysočina Region, Predborice, and Koksin Hill, Czech Republic; Puy-de-Dôme, France; Kalmar, Sweden; La Rioja Province, Argentina; and most recently Zaire (Democratic Republic of Congo); all of which were found in or near uranium mines. In Canada, athabascaite is commonly associated with umangite, clausthalite, eucairite, berzelianite, sulfatian berzelianite, klockmannite, eskebornite, tyrrellite, native copper, native silver, uraninite, hematite, pyrite, calcite, barite, quartz and feldspar. In Argentina and Sweden, it is associated with umangite and berzelianite. In the Czech Republic, it occurs with berzelianite, eucairite, crookesite, tyrrellite, ferroselite, bukovite, krutaite, calcite and dolomite. In Zaire, it is associated with digenite, berzelianite, yarrowite, spionkopite, trogtalite, native copper and native gold.[6]

References

  1. Entry on Mindat.org
  2. Entry on Webmineral
  3. Handbook of Mineralogy
  4. 1 2 3 Harris, D.C., Cabri, L.J., and Kaiman, S. (1970) Athabascaite: A New Copper Selenide Mineral from Martin Lake, Saskatchewan. The Canadian Mineralogist, 10(2), 207-215.
  5. Earley, J.W. (1950) Description and Synthesis of the Selenide Minerals. The American Mineralogist 35(5&6), 337-364.
  6. 1 2 Johan, Z., Picot, P., and Ruhlmann, F. (1982) Evolution paragenetique de la mineralization uranifere de Chameans (Puy-de-Dôme) France: Chameanite, Geffroyite et Girauditem Trios Seleniures Nouvease de Cu, Fe, Ag, and As. Tshermaks Moneral. Petrog. Mitt., 29, 151-167.
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