Barytocalcite | |
---|---|
General | |
Category | Carbonate mineral |
Formula (repeating unit) | BaCa(CO3)2 |
IMA symbol | Bcal [1] |
Strunz classification | 5.AB.45 |
Dana classification | 14.02.06.01 |
Crystal system | Monoclinic |
Crystal class | Prismatic (2/m) (same H-M symbol) |
Space group | P21/m |
Unit cell | a = 8.1 Å, b = 5.2 Å, c = 6.5 Å, β = 106°; Z = 2 |
Identification | |
Formula mass | 297.42 g/mol [2] |
Colour | Colourless, white, greyish, greenish, yellowish |
Crystal habit | Prismatic, drusy, massive – granular |
Cleavage | Perfect in at least two directions [2] [3] |
Tenacity | Brittle |
Mohs scale hardness | 4 |
Luster | Vitreous to resinous |
Streak | White |
Diaphaneity | Translucent to transparent |
Specific gravity | 3.64 to 3.71 |
Optical properties | Biaxial (−) |
Refractive index | nα = 1.525, nβ = 1.684, nγ = 1.686 |
Birefringence | δ = 0.161 [4] |
2V angle | Measured: 15°, calculated: 10° |
Dispersion | Relatively weak, r>v |
Ultraviolet fluorescence | Fluorescent dull yellow under LW and SW UV [4] |
Solubility | Soluble in dilute HCl [4] |
References | [2] [3] [4] [5] |
Barytocalcite is an anhydrous barium calcium carbonate mineral with the chemical formula Ba Ca(C O 3)2. It is trimorphous with alstonite and paralstonite, that is to say the three minerals have the same formula but different structures. [3] Baryte and quartz pseudomorphs after barytocalcite have been observed. [4]
Barytocalcite crystallizes in the monoclinic crystal system, typically as massive to druzy accumulations of transparent white to yellow to grey aggregates of slender prismatic crystals. It has a Mohs hardness of 4 and a specific gravity of 3.64 to 3.71. [4]
It was first described in 1824 for an occurrence in the Blagill Mine in North Pennines, Cumbria (Cumberland), England, and named for its composition.
The mineral crystallises in the monoclinic crystal system. Most sources [3] [4] [5] put it in the prismatic class 2/m, with space group P21/m, but Webmin [2] puts it in the sphenoidal class 2 with space group P21. The structure is similar to that of dolomite, but with two crystallographically different CO3 groups. [3] The cation layers are stacked in an ABCABC... stacking pattern, repeating every 3 layers. The Ca ion is coordinated to 7 oxygens. [5]
All sources give unit cell parameters whose values rounded down are a = 8.1 Å, b = 5.2 Å, c = 6.5 Å and β = 106°, with two formula units per unit cell (Z = 2). The primary source [5] has a = 8.092 Å, b = 5.2344 Å, c = 6.544 Å, β = 106.05° and Z=2.
Barytocalcite often forms oriented growths on baryte, and calcite, witherite and baryte can be epitaxial on barytocalcite. [3] [4] Crystals are normally short to long prismatic and striated. They are transparent to translucent, colourless, white, greyish, greenish or yellowish with a white streak and a vitreous to resinous lustre.
Barytocalcite is a biaxial (-) mineral with refractive indices nα = 1.525, nβ = 1.684 and nγ = 1.686. The maximum birefringence (the difference in refractive index between light travelling through the crystal with different polarizations) is δ = 0.161. [4] The optic angle 2V is the angle between the two optic axes in a biaxial crystal. The measured values of 2V for this mineral is 15°. It is also possible to calculate a theoretical value of 2V from the measured values of the refractive indices. The calculated value for barytocalcite is 10°. If the colour of the incident light is changed, then the refractive indices are modified, and the value of 2V changes. This is known as dispersion of the optic axes. For barytocalcite the effect is weak, with 2V larger for red light than for violet light (r>v). [3]
The optical directions X, Y and Z are the directions of travel of light with refractive indices nα, nβ and nγ respectively. In general they are not the same as the directions a, b and c of the crystallographic axes. For barytocalcite Z is parallel to the b axis, X is at an angle of 64° to the c axis and Y is at an angle of 26° to the c axis. [3]
Sources disagree about fluorescence. Webmin [2] describes the mineral as non-fluorescent, Dana [3] categorises it as weakly fluorescent and Mindat [4] states that it is fluorescent dull yellow under both longwave and shortwave ultraviolet light.
Barytocalcite has at least one perfect and one imperfect cleavage. [2] [3] It is a brittle mineral, and breaks with an uneven to conchoidal fracture. It is quite soft, with a hardness 4, the same as that of fluorite. Calcite CaCO3 and dolomite CaMg(CO3)2 are carbonates where calcium Ca and magnesium Mg replace the barium in the formula for barytocalcite, BaCa(CO3)2. These two minerals are even softer than barytocalcite, and much less dense. Barytocalcite has specific gravity 3.7. This is higher than that of calcite (2.7) or dolomite (2.85) because the barium atom is very heavy, with atomic mass 137, which is much more than magnesium at 24 and calcium at 40. Barytocalcite is soluble in dilute hydrochloric acid HCl [4] and it is not radioactive. [2]
The type locality is the Blagill Mine, Nent Valley, Alston Moor District, North Pennines, North and Western Region, Cumbria, England. This mine is no longer operative, and it has been designated a site of Site of Special Scientific Interest so collecting is no longer allowed. In the past lustrous, transparent, prismatic crystals of barytocalcite have been found there [6] in veins in limestone, associated with fluorite, calcite and baryte. [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.
Vivianite (Fe2+
3(PO
4)
2·8H
2O) is a hydrated iron phosphate mineral found in a number of geological environments. Small amounts of manganese Mn2+, magnesium Mg2+, and calcium Ca2+ may substitute for iron Fe2+ in the structure. Pure vivianite is colorless, but the mineral oxidizes very easily, changing the color, and it is usually found as deep blue to deep bluish green prismatic to flattened crystals.
Vivianite crystals are often found inside fossil shells, such as those of bivalves and gastropods, or attached to fossil bone.
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.
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.
Beryllonite is a rare sodium beryllium phosphate mineral with formula NaBePO4. The tabular to prismatic monoclinic crystals vary from colorless to white or pale yellowish, and are transparent with a vitreous luster. Twinning is common and occurs in several forms. It exhibits perfect cleavage in one direction. The hardness is 5.5 to 6 and the specific gravity is 2.8. Refractive indices are nα = 1.552, nβ = 1.558 and nγ = 1.561. A few crystals have been cut and faceted, but, as the refractive index is no higher than that of quartz, they do not make very brilliant gemstones.
Haidingerite is a calcium arsenate mineral with formula Ca(AsO3OH)·H2O. It crystallizes in the orthorhombic crystal system as short prismatic to equant crystals. It typically occurs as scaly, botryoidal or fibrous coatings. It is soft, Mohs hardness of 2 to 2.5, and has a specific gravity of 2.95. It has refractive indices of nα = 1.590, nβ = 1.602 and nγ = 1.638.
Mesolite is a tectosilicate mineral with formula Na2Ca2(Al2Si3O10)3·8H2O. It is a member of the zeolite group and is closely related to natrolite which it also resembles in appearance.
Zircophyllite is a complex mineral, formula (K,Na)3(Mn,Fe)2+7(Zr,Ti,Nb)2Si8O24(OH,F)7. It crystallizes in the triclinic - pinacoidal crystal class as dark brown to black micaceous plates. It has perfect 001 cleavage, a Mohs hardness of 4 to 4.5 and a specific gravity of 3.34. Its indices of refraction are nα=1.708 nβ=1.738 nγ=1.747 and it has a 2V optical angle of 62°.
Nyerereite is a very rare sodium calcium carbonate mineral with formula Na2Ca(CO3)2. It forms colorless, platey pseudohexagonal orthorhombic crystals that are typically twinned. It has a specific gravity of 2.54 and indices of refraction of nα=1.511, nβ=1.533 and nγ=1.535. Nyerereite is not stable in contact with the atmosphere and rapidly breaks down. Collection specimens must be kept in a sealed argon environment.
Pumpellyite is a group of closely related sorosilicate minerals:
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.
Keyite is a mineral with the chemical formula Cu2+3Zn4Cd2(AsO4)6 · 2H2O. The name comes from Charles Locke Key, an American mineral dealer who furnished its first specimens. Keyite is monoclinic-prismatic, meaning its crystal form has three unequal axes, two of which have 90° angles between them and one with an angle less than 90°. Keyite belongs to the biaxial optical class, meaning it has more than one axis of anisotropy, in which light travels with zero birefringence, and three indices of refraction, nα = 1.800, nβ, and nγ = 1.870. Being a very rare cadmium copper arsenate, keyite is only found in Tsumeb, Namibia in the Tsumeb mine, a world-famous copper mine known for its abundance of rare and unusual minerals.
Magnesiohastingsite is a calcium-containing amphibole and a member of the hornblende group. It is an inosilicate (chain silicate) with the formula NaCa2(Mg4Fe3+)(Si6Al2)O22(OH)2 and molar mass 864.69 g. In synthetic magnesiohastingsite it appears that iron occurs both as ferrous iron Fe2+ and as ferric iron Fe3+, but the ideal formula features only ferric iron. It was named in 1928 by Marland P. Billings. The name is for its relationship to hastingsite and its magnesium content. Hastingsite was named for the locality in Dungannon Township, Hastings County, Ontario, Canada.
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).
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.
Rampgill mine is a disused lead mine at Nenthead, Alston Moor, Cumbria, England UK Grid Reference: NY78184351
Carminite (PbFe3+2(AsO4)2(OH)2) is an anhydrous arsenate mineral containing hydroxyl. It is a rare secondary mineral that is structurally related to palermoite (Li2SrAl4(PO4)4(OH)4). Sewardite (CaFe3+2(AsO4)2(OH)2) is an analogue of carminite, with calcium in sewardite in place of the lead in carminite. Mawbyite is a dimorph (same formula, different structure) of carminite; mawbyite is monoclinic and carminite is orthorhombic. It has a molar mass of 639.87 g. It was discovered in 1850 and named for the characteristic carmine colour.
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.
Mottramite is an orthorhombic anhydrous vanadate hydroxide mineral, PbCu(VO4)(OH), at the copper end of the descloizite subgroup. It was formerly called cuprodescloizite or psittacinite (this mineral characterized in 1868 by Frederick Augustus Genth). Duhamelite is a calcium- and bismuth-bearing variety of mottramite, typically with acicular habit.
Talmessite is a hydrated calcium magnesium arsenate, often with significant amounts of cobalt or nickel. It was named in 1960 for the type locality, the Talmessi mine, Anarak district, Iran. It forms a series with β-Roselite, where cobalt replaces some of the magnesium, and with gaitite, where zinc replaces the magnesium. All these minerals are members of the fairfieldite group. Talmessite is dimorphic with wendwilsonite.