Athabascaite

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Athabascaite
Athabascaite.jpg
General
Category Selenide mineral
Formula
(repeating unit)
Cu5Se4
IMA symbol Atb [1]
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
ColorLight grey, bluish-gray to white
Crystal habit As anhedral inclusions and lath shaped crystals, also massive
Mohs scale hardness2.5
Luster Metallic
Diaphaneity Opaque
Specific gravity 6.59 (calculated)
Optical propertiesAnisotropism strong, creamy white to dark blue
Pleochroism Distinct, pale gray to blue-gray
References [2] [3] [4]

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. [5]

Contents

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. [6]

Structure

Because of unavailability 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. [5]

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. [5]

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. [7]

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. [7]

Related Research Articles

<span class="mw-page-title-main">Mineral</span> Crystalline chemical element or compound formed by geologic processes

In geology and mineralogy, a mineral or mineral species is, broadly speaking, a solid substance with a fairly well-defined chemical composition and a specific crystal structure that occurs naturally in pure form.

<span class="mw-page-title-main">Calcite</span> Calcium carbonate mineral

Calcite is a carbonate mineral and the most stable polymorph of calcium carbonate (CaCO3). It is a very common mineral, particularly as a component of limestone. Calcite defines hardness 3 on the Mohs scale of mineral hardness, based on scratch hardness comparison. Large calcite crystals are used in optical equipment, and limestone composed mostly of calcite has numerous uses.

<span class="mw-page-title-main">Bornite</span> Sulfide mineral

Bornite, also known as peacock ore, is a sulfide mineral with chemical composition Cu5FeS4 that crystallizes in the orthorhombic system (pseudo-cubic).

<span class="mw-page-title-main">Dioptase</span>

Dioptase is an intense emerald-green to bluish-green copper cyclosilicate mineral. It is transparent to translucent. Its luster is vitreous to sub-adamantine. Its formula is Cu6Si6O18·6H2O (also reported as CuSiO2(OH)2). It has a hardness of 5, the same as tooth enamel. Its specific gravity is 3.28–3.35, and it has two perfect and one very good cleavage directions. Additionally, dioptase is very fragile, and specimens must be handled with great care. It is a trigonal mineral, forming 6-sided crystals that are terminated by rhombohedra.

<span class="mw-page-title-main">Tennantite</span> Copper arsenic sulfosalt mineral

Tennantite is a copper arsenic sulfosalt mineral with an ideal formula Cu12As4S13. Due to variable substitution of the copper by iron and zinc the formula is Cu6[Cu4(Fe,Zn)2]As4S13. It is gray-black, steel-gray, iron-gray or black in color. A closely related mineral, tetrahedrite (Cu12Sb4S13) has antimony substituting for arsenic and the two form a solid solution series. The two have very similar properties and is often difficult to distinguish between tennantite and tetrahedrite. Iron, zinc, and silver substitute up to about 15% for the copper site.

<span class="mw-page-title-main">Torbernite</span> Copper uranyl phosphate mineral

Torbernite, also known as chalcolite, is a relatively common mineral with the chemical formula Cu[(UO2)(PO4)]2(H2O)12. It is a radioactive, hydrated green copper uranyl phosphate, found in granites and other uranium-bearing deposits as a secondary mineral. The chemical formula of torbernite is similar to that of autunite in which a Cu2+ cation replaces a Ca2+ cation. Torbernite tends to dehydrate to metatorbernite with the sum formula Cu[(UO2)(PO4)]2(H2O)8.

<span class="mw-page-title-main">Artinite</span> Hydrated basic magnesium carbonate mineral

Artinite is a hydrated basic magnesium carbonate mineral with formula: Mg2(CO3)(OH)2·3H2O. It forms white silky monoclinic prismatic crystals that are often in radial arrays or encrustations. It has a Mohs hardness of 2.5 and a specific gravity of 2.

WyartiteCaU5+
(UO
2
)
2
(CO
3
)O
4
(OH)
·7H2O is a uranium bearing mineral named after Jean Wyart (1902–1992), mineralogist at the Sorbonne, Paris. It has greenish-black, black, or violet-black, translucent to opaque orthorhombic crystals. A hardness of 3 - 4 Mohs. Its other names are Ianthinite (of Bignand), Wyartit and Wyartita. It belongs to the uranium carbonate group of minerals. It is found next to rutherfordine in Shinkolobwe, Shaba, Zaire.

<span class="mw-page-title-main">Kutnohorite</span> Mineral of calcium manganese carbonate

Kutnohorite is a rare calcium manganese carbonate mineral with magnesium and iron that is a member of the dolomite group. It forms a series with dolomite, and with ankerite. The end member formula is CaMn2+(CO3)2, but Mg2+ and Fe2+ commonly substitute for Mn2+, with the manganese content varying from 38% to 84%, so the formula Ca(Mn2+,Mg,Fe2+)(CO3)2 better represents the species. It was named by Professor Bukowsky in 1901 after the type locality of Kutná Hora, Bohemia, in the Czech Republic. It was originally spelt "kutnahorite" but "kutnohorite" is the current IMA-approved spelling.

<span class="mw-page-title-main">Carrollite</span> Mineral

Carrollite, CuCo2S4, is a sulfide of copper and cobalt, often with substantial substitution of nickel for the metal ions, and a member of the linnaeite group. It is named after the type locality in Carroll County, Maryland, US, at the Patapsco mine, Sykesville.

<span class="mw-page-title-main">Penroseite</span>

Penroseite is a rare selenide mineral with formula (Ni,Co,Cu)Se2. It has a gray-steel color and black streak with a hardness of 3. It is an isometric mineral, 2/m3. Penroseite was first discovered in 1925 in a Bolivian rhyolite. It was named for Richard Penrose (1863–1931), an economic geologist.

Cleusonite is a member of the crichtonite group of minerals with the chemical formula (Pb,Sr)(U4+
,U6+
)(Fe2+
,Zn)
2
(Ti,Fe2+
,Fe3+
)
18
(O,OH)
38
. This group of minerals contains approximately thirteen complex metal titanates. The structures of minerals of this group is complicated by frequent fine-scale twinning and metamictization due to radioactive elements. The crichtonite group consists of members of related mineral species of the type A{BC2D6E12}O38 which are characterized by their predominant cations (as seen in crichtonite (Sr), senaite (Pb), davidite (REE + U), landauite (Na), loveringite (Ca), lindsleyite (Ba), and mathiasite (K).

Jolliffeite is a rare selenide mineral with formula NiAsSe or (Ni,Co)AsSe. It is the selenium analogue of the sulfide mineral gersdorffite, NiAsS, with a common impurity of cobalt, CoAsSe. It is named for its discoverer, Alfred Jolliffe, (1907–1988), a Canadian geologist of Queen's University, Kingston, Ontario.

<span class="mw-page-title-main">Tyrrellite</span>

Tyrrellite is a selenide mineral that has a chemical formula of Cu(Co,Ni)2Se4. It has been found in the Goldfields District in northern Saskatchewan, as well as in the Petrovice deposit, Czech Republic. It is named after the Canadian geologist Joseph Burr Tyrrell. Joseph Tyrrell was one of the first geologists from the Geological Survey of Canada to do research in the Goldfields District.

<span class="mw-page-title-main">Donnayite-(Y)</span> Rare-earth carbonate mineral containing the rare-earth metal yttrium

Donnayite-(Y) is a rare-earth carbonate mineral containing the rare-earth metal yttrium. It was first discovered in 1978 at Mont Saint-Hilaire, Quebec. Donnayite was subsequently identified and named after Joseph D. H. Donnay and his wife, Gabrielle Donnay. Both were prominent mineralogists and crystallographers, and J. D. H. Donnay was awarded the Roebling Award by the Mineralogical Society of America in 1971 for his emphasis on the importance of optical mineralogy and crystal morphology. Donnayite tends to occur in small quantities in the pegmatite dykes and miarolitic cavities of mountainous regions. It crystallizes in this environment with increasing alkalinity values until the alkalinity suddenly drops during the last stage of crystallization. This results in increasing amounts of Na carbonates and REE minerals. First discovered at Mont St-Hilaire, donnayite has since been found in the Southern Ural Mountains of Russia and the Narssarssuk pegmatite of South Greenland. Donnayite crystals tend to be small and the color is commonly pale yellow to yellow with a white streak and a vitreous luster. Donnayite crystals usually display trigonal or hexagonal symmetry and have a hardness of 3. Twinning is extremely common in this mineral. Minerals closely related to donnayite include synchysite, calcite, sphalerite, microcline, and analcime. Donnayite is isomorphous with weloganite and mckelveyite.

Chrisstanleyite, Ag2Pd3Se4, is a selenide mineral that crystallizes in high saline, acidic hydrothermal solution at low temperatures as part of selenide vein inclusions in and alongside calcite veins. It tends to be found in assemblages of other selenides: jagueite, naumannite, fischesserite, oosterboschite, and tiemannite, and it is a solid solution mineral with jagueite Cu2Pd3Se4 in which it shares a unique crystal structure that has not been identified elsewhere (Paar et al. 1998; Nickel 2002; Paar et al. 2004). Chrisstanleyite and jagueite are unlike the other minerals of the selenide family as they do not have a sulfide analogue (Topa et al. 2006). First discovered by Werner Paar from a sample received from Hope's Nose, Torquay, Devon, England, chrisstanleyite has since been discovered in the Pilbara region of Western Australia and in El Chire, La Rioja, Argentina. Chrisstanleyite was named after the Deputy Head and Associate Keeper at the Department of Mineralogy at The Natural History Museum in London.

Bijvoetite-(Y) is a very rare rare-earth and uranium mineral with the formula (Y,REE)8(UO2)16(CO3)16O8(OH)8·39H2O. When compared to the original description, the formula of bijvoetite-(Y) was changed in the course of crystal structure redefinition. Bijvoetite-(Y) is an example of natural salts containing both uranium and yttrium, the other examples being kamotoite-(Y) and sejkoraite-(Y). Bijvoetite-(Y) comes from Shinkolobwe deposit in Republic of Congo, which is famous for rare uranium minerals. The other interesting rare-earth-bearing uranium mineral, associated with bijvoetite-(Y), is lepersonnite-(Gd).

Copper selenide is an inorganic binary compound between copper and selenium. The chemical formula depends on the ratio between the two elements, such as CuSe or Cu2Se.

<span class="mw-page-title-main">Kruťaite</span>

Kruťaite, simplified Krut'aite or krutaite, is a rare mineral with the formula CuSe2. It crystallises in the cubic crystal system. It is part of the pyrite group, being composed of Cu2+ ions and Se22− ions. The mineral is most often found as a dark grey aggregate consisting of tiny crystals no more than a millimeter in size. The crystals are opaque in any size. It has no industrial use, but it is a prized collector's item.

<span class="mw-page-title-main">Berzelianite</span>

Berzelianite is a rare copper selenide mineral with the formula Cu2Se. It occurs as thin dendritic crusts or as fine-grained inclusions. It crystallizes in the isometric system, unlike its dimorph, bellidoite, which crystallizes in the tetragonal system. The crystals are opaque and slightly malleable.

References

  1. 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.
  2. Entry on Mindat.org
  3. Entry on Webmineral
  4. Handbook of Mineralogy
  5. 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.
  6. Earley, J.W. (1950) Description and Synthesis of the Selenide Minerals. The American Mineralogist 35(5&6), 337–364.
  7. 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.