Brianyoungite | |
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General | |
Category | Carbonate mineral |
Formula (repeating unit) | Zn3(CO3,SO4)(OH)4 [1] |
IMA symbol | Byo [2] |
Strunz classification | 5.BF.30 (10 ed) 5/C.01-105 (8 ed) |
Dana classification | 17.1.15 |
Crystal system | Monoclinic |
Crystal class | Prismatic (2/m) (same H-M symbol) |
Space group | C2/m |
Unit cell | 15.724 Å, b = 6.256 Å, c = 5.427 Å; β = 90°; Z = 4 |
Identification | |
Color | White |
Crystal habit | Rosettes of thin blades, pseudo-orthorhombic with β close to 90° [3] |
Cleavage | Perfect on {100}, possible on {001} [3] [4] |
Mohs scale hardness | 2 to 2.5 |
Luster | Vitreous |
Streak | White |
Diaphaneity | Transparent to translucent |
Specific gravity | 3.93 to 4.09 |
Optical properties | Biaxial |
Refractive index | nω = 1.635, nε = 1.650 |
Birefringence | δ = 1.635 [5] |
Solubility | Readily soluble with effervescence in acids [3] |
Other characteristics | Non-fluorescent [3] |
References | [1] [6] [3] [4] [5] [7] |
Brianyoungite is a secondary zinc carbonate mineral. The Commission on New Minerals, Nomenclature and Classification (CNMNC) of the International Mineralogical Association (IMA) classifies it as a carbonate with the formula Zn3(CO3)(OH)4, [1] but sulfate groups SO4 also occupy the carbonate CO3 positions, in the ratio of about one sulfate to three carbonates, [3] so other sources give the formula as Zn3(CO3,SO4)(OH)4, and Gaines et al. classify the mineral as a compound carbonate. [7] It is similar in appearance to hydrozincite, another zinc carbonate. [5] It was discovered in 1991 and designated IMA1991-053. [5] In 1993 it was named "brianyoungite" after Brian Young (born 1947), a field geologist with the British Geological Survey, who provided the first specimens. [4] [7]
The mineral occurs as tiny rosettes less than 100 μm across, composed of thin blades just one or two micrometers across, elongated parallel to the b crystal axis, and tapering to a sharp point. [3] The crystals are white and transparent to translucent, with a vitreous lustre and a white streak.
The mineral belongs in the orthorhombic crystal system, or the monoclinic with β (the angle between the a and c crystal axes) close to 90o. [3] The space group is unknown, but assumed to be either P21/m, P21 or P2221. [4] [5] The structure is similar to that of hydrozincite. [7] There are four formula units per unit cell (Z = 4) and the lengths of the sides of the unit cell are a = 15.724 Å, b = 6.256 Å and c = 5.427 Å. [3]
Brianyoungite is a soft mineral with Mohs hardness similar to halite, only 2 to 2+1⁄2 according to some sources, [6] [5] but others say that the hardness is not determinable. [3] [4] It is fairly dense, with specific gravity 3.93 to 4.09, similar to that of celestine. Cleavage is perfect perpendicular to the a crystal axis (perfect on {100}) and possible perpendicular to the c crystal axis (possible on {001}). [3] [4] It is readily soluble with effervescence in acids. [3]
The mineral is biaxial, with refractive indices nω = 1.635 and nε = 1.650 and maximum birefringence δ = 1.635. [5] It exhibits straight extinction. [3] It is not fluorescent. [3]
The type locality is the Bloomsberry Horse level of the Brownley Hill mine, Nenthead, Alston Moor District, North Pennines, North and Western Region (Cumberland), Cumbria, England. [5] The type material is conserved at the Royal Museum of Scotland, Edinburgh, Scotland, 1992.17.1–8. [4]
Brianyoungite occurs with gypsum on rubbly limestone in the oxidised zone of Brownley Hill Mine, and on specimens from the nearby Smallcleugh mine. [3] It may be a secondary post-mining mineral. [6] [4] At the type locality it is associated with gypsum, smithsonite, pyrite and goethite. [4]
Strontianite (SrCO3) is an important raw material for the extraction of strontium. It is a rare carbonate mineral and one of only a few strontium minerals. It is a member of the aragonite group.
Alstonite, also known as bromlite, is a low temperature hydrothermal mineral that is a rare double carbonate of calcium and barium with the formula BaCa(CO
3)
2, sometimes with some strontium. Barytocalcite and paralstonite have the same formula but different structures, so these three minerals are said to be trimorphous. Alstonite is triclinic but barytocalcite is monoclinic and paralstonite is trigonal. The species was named Bromlite by Thomas Thomson in 1837 after the Bromley-Hill mine, and alstonite by August Breithaupt of the Freiberg Mining Academy in 1841, after Alston, Cumbria, the base of operations of the mineral dealer from whom the first samples were obtained by Thomson in 1834. Both of these names have been in common use.
Barytocalcite is an anhydrous barium calcium carbonate mineral with the chemical formula BaCa(CO3)2. It is trimorphous with alstonite and paralstonite, that is to say the three minerals have the same formula but different structures. Baryte and quartz pseudomorphs after barytocalcite have been observed.
Leadhillite is a lead sulfate carbonate hydroxide mineral, often associated with anglesite. It has the formula Pb4SO4(CO3)2(OH)2. Leadhillite crystallises in the monoclinic system, but develops pseudo-hexagonal forms due to crystal twinning. It forms transparent to translucent variably coloured crystals with an adamantine lustre. It is quite soft with a Mohs hardness of 2.5 and a relatively high specific gravity of 6.26 to 6.55.
Hanksite is a sulfate mineral, distinguished as one of only a handful that contain both carbonate and sulfate ions (a sulfate carbonate). It has the chemical formula Na22K(SO4)9(CO3)2Cl.
Zincobotryogen is a hydrous sulfate mineral with the chemical formula (Zn,Mg,Mn)Fe3+(SO4)2(OH)·7H2O. It forms bright orange red monoclinic prismatic crystals that exhibit a vitreous to greasy luster. Its specific gravity is 2.201 and it has a Mohs hardness of 2.5.
Ettringite is a hydrous calcium aluminium sulfate mineral with formula: Ca6Al2(SO4)3(OH)12·26H2O. It is a colorless to yellow mineral crystallizing in the trigonal system. The prismatic crystals are typically colorless, turning white on partial dehydration. It is part of the ettringite-group which includes other sulfates such as thaumasite and bentorite.
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.
Thaumasite is a calcium silicate mineral, containing Si atoms in unusual octahedral configuration, with chemical formula Ca3Si(OH)6(CO3)(SO4)·12H2O, also sometimes more simply written as CaSiO3·CaCO3·CaSO4·15H2O.
Mosesite is a very rare mineral found in few locations. It is a mercury mineral found as an accessory in deposits of mercury, often in conjunction with limestone. It is known to be found in the U.S. states of Texas and Nevada, and the Mexican states of Guerrero and Querétaro. It was named after Professor Alfred J. Moses (1859–1920) for his contributions to the field of mineralogy in discovering several minerals found alongside mosesite. The mineral itself is various shades of yellow and a high occurrence of spinel twinning. It becomes isotropic when heated to 186 °C (367 °F).
Reinerite is a rare arsenite (arsenate(III)) mineral with chemical formula Zn3(AsO3)2. It crystallizes in the orthorhombic crystal system.
Tsumebite is a rare phosphate mineral named in 1912 after the locality where it was first found, the Tsumeb mine in Namibia, well known to mineral collectors for the wide range of minerals found there. Tsumebite is a compound phosphate and sulfate of lead and copper, with hydroxyl, formula Pb2Cu(PO4)(SO4)(OH). There is a similar mineral called arsentsumebite, where the phosphate group PO4 is replaced by the arsenate group AsO4, giving the formula Pb2Cu(AsO4)(SO4)(OH). Both minerals are members of the brackebuschite group.
Bayleyite is a uranium carbonate mineral with the chemical formula: Mg2(UO2)(CO3)3·18(H2O). It is a secondary mineral which contains magnesium, uranium and carbon. It is a bright yellow color. Its crystal habit is acicular but is more commonly found as crusts on uranium bearing ores. It has a Mohs hardness of about 2–2.5.
Rapidcreekite is a rare mineral with formula Ca2(SO4)(CO3)·4H2O. The mineral is white to colorless and occurs as groupings of acicular (needle-shaped) crystals. It was discovered in 1983 in northern Yukon, Canada, and described in 1986. Rapidcreekite is structurally and compositionally similar to gypsum.
Ianbruceite is a rare hydrated zinc arsenate with the formula [Zn2(OH)(H2O)(AsO4)](H2O)2; material from the Driggith mine has traces of cobalt. It was first discovered at Tsumeb, approved by the International Mineralogical Association as a new mineral species in 2011, reference IMA2011-49, and named for Ian Bruce, who founded "Crystal Classics" in the early 1990s, and was heavily involved in attempts to reopen the famous Tsumeb mine for specimen mining.
In 2013 new occurrences of ianbruceite were reported from the neighbouring Driggith and Potts Gill mines on High Pike in the Caldbeck Fells, Cumbria, England. Here the mineral is probably a post-mining product. Caldbeck Fells and Tsumeb are the only reported localities for ianbruceite to date (May 2013).
Gordaite is a sulfate mineral composed primarily of hydrous zinc sodium sulfate chloride hydroxide with formula: NaZn4(SO4)(OH)6Cl·6H2O. It was named for the discovery location in the Sierra Gorda district of Chile. Gordaite forms as tabular trigonal crystals.
Köttigite is a rare hydrated zinc arsenate which was discovered in 1849 and named by James Dwight Dana in 1850 in honour of Otto Friedrich Köttig (1824–1892), a German chemist from Schneeberg, Saxony, who made the first chemical analysis of the mineral. It has the formula Zn3(AsO4)2·8H2O and it is a dimorph of metaköttigite, which means that the two minerals have the same formula, but a different structure: köttigite is monoclinic and metaköttigite is triclinic. There are several minerals with similar formulae but with other cations in place of the zinc. Iron forms parasymplesite Fe2+3(AsO4)2·8H2O; cobalt forms the distinctively coloured pinkish purple mineral erythrite Co3(AsO4)2·8H2O and nickel forms annabergite Ni3(AsO4)2·8H2O. Köttigite forms series with all three of these minerals and they are all members of the vivianite group.
Serpierite (Ca(Cu,Zn)4(SO4)2(OH)6·3H2O) is a rare, sky-blue coloured hydrated sulfate mineral, often found as a post-mining product. It is a member of the devilline group, which has members aldridgeite (Cd,Ca)(Cu,Zn)4(SO4)2(OH)6·3H2O, campigliaite Cu4Mn2+(SO4)2(OH)6·4H2O, devilline CaCu4(SO4)2(OH)6·3H2O, kobyashevite Cu5(SO4)2(OH)6·4H2O, lautenthalite PbCu4(SO4)2(OH)6·3H2O and an unnamed dimorph of devilline. It is the calcium analogue of aldridgeite and it is dimorphous with orthoserpierite CaCu4(SO4)2(OH)6·3H2O.
Macphersonite, Pb4(SO4)(CO3)2 (OH)2, is a carbonate mineral that is trimorphous with leadhillite and susannite. Macphersonite is generally white, colorless, or a pale amber in color and has a white streak. It crystallizes in the orthorhombic system with a space group of Pcab. It is fairly soft mineral that has a high specific gravity.
Meyrowitzite, Ca(UO2)(CO3)2·5H2O, is a carbonate mineral verified in May of 2018 by the Commission of New Minerals, Nomenclature and Classification of the International Mineralogical Association. It is an extremely rare mineral, discovered in the Markey mine Utah, U.S.A. The mineral is a transparent yellow and has blades up to approximately 0.2 mm in length. It is soluble in water or aqueous solutions. Meyrowitzite is named in honor of Robert Meyrowitz (1916–2013), an American analytical chemist. After serving in WW II, he joined the United States Geological Survey (USGS). He was known for developing innovative new methods for analyzing small and difficult to study mineralogical samples along with his formulation of the high-index immersion liquids.