Tuperssuatsiaite | |
---|---|
General | |
Category | Phyllosilicate |
Formula (repeating unit) | NaFe3+3Si8O20(OH)2·H2O [1] |
IMA symbol | Tup [2] |
Strunz classification | 9.EE.20 |
Dana classification | 74.3.1a.2 |
Crystal system | Monoclinic |
Crystal class | Prismatic (2/m) (same H-M symbol) |
Space group | C2/m |
Unit cell | a = 13.72 Å, b = 18 Å c = 4.82 Å; β = 104.28°; Z = 2 |
Identification | |
Formula mass | 818.31 g/mol |
Color | Dark to light red-brown |
Crystal habit | Fan-shaped aggregates, rosettes or fibers |
Twinning | Common |
Cleavage | Good on {100} |
Fracture | Uneven to conchoidal |
Tenacity | Brittle |
Mohs scale hardness | Not determined |
Luster | Vitreous |
Streak | Brownish yellow |
Diaphaneity | Transparent |
Specific gravity | 2.465 |
Optical properties | Biaxial (+) |
Refractive index | nα = 1.539, nβ = 1.560, nγ = 1.595 |
Birefringence | δ = 0.056 |
Pleochroism | Colorless to yellowish brown or reddish brown |
2V angle | Measured: 103° to 103°, Calculated: 78° |
Other characteristics | Neither radioactive [3] nor fluorescent [4] |
References | [3] [5] [6] [7] |
Tuperssuatsiaite is a rare clay mineral found in Greenland, Namibia and Brazil. It is a hydrated phyllosilicate (sheet silicate) of sodium and iron.
Tuperssuatsiaite was first found by Karup-Moller and Petersen in Greenland, in 1984, and given the International Mineralogical Association designation IMA1984-002. It was later named after the type locality, Tuperssuatsiat Bay, Ilimaussaq, Greenland. [4] In 1992 Karup-Moller and Petersen, together with von Knorring and Leonardsen, found more specimens from a second find in the Aris Quarry in Namibia, that allowed a better definition of the properties and composition of the mineral. [8] Later still, in 2005, more material was found by a group of researchers from the University of São Paulo at the Bortolan Quarry, Pocos de Caldas, Brazil, and although the crystals were small, accurate determinations were made of their physical and optical properties, which differed slightly from those of the specimens from Greenland and Namibia. [9]
Tuperssuatsiaite is a member of the palygorskite-sepiolite group, palygorskite subgroup.
Subgroup members (formulae according to the IMA [1] ):
Iron occurs both in the ferric state Fe3+ and the ferrous state Fe2+. The formula for tuperssuatsiaite contains only ferric iron, and the Greenland material is consistent with this. Analysis of the Namibian material, however, shows that part of the iron is in the ferrous state. [5] Manganese is also present as a substitute for iron, [5] and a zinc-rich material has been reported from Greenland. [4]
The mineral belongs to the monoclinic crystal class 2/m, meaning that it has a twofold axis of rotational symmetry perpendicular to a mirror plane. At one time it was thought that the material from Namibia might belong to the monoclinic class 2, without the mirror plane, [8] but a more recent study gives it as 2/m, the same as the material from Greenland. [10]
The space group is B2/m, meaning that in the unit cell there is one structural unit at each vertex, and one in the centre of each B face. The palygorskite-sepiolite minerals are clay minerals with a layered structure. In tuperssuatsiaite ribbons of SiO4 tetrahedra, similar to those in the amphibole structure, are aligned parallel to the c crystal axis, and they link to form layers parallel to the plane containing the a and b axes. [10] The spacing between the layers, in the c direction, is about 5 Å, which is typical for minerals with an amphibole-type structure, due to the repeat distance along the chains of tetrahedra. [5] Channels occur that could be occupied by H2O as in palygorskite. [10]
There are two formula units per unit cell (Z = 2), and the cell dimensions vary slightly for specimens from different locations; for all specimens, to the nearest Å, a = 14 Å, b = 18 Å and c = 5 Å, and the angle β = 103° to 105°.
For the three main localities the reported values are:
Tuperssuatsiaite occurs as fan-shaped aggregates up to several centimeters across, as rosettes and as fibers elongated parallel to the c axis. [4] It is red-brown in reflected light, and colorless to light yellowish brown in transmitted light, with a brownish yellow streak. Crystals are transparent with a bright vitreous luster, but aggregates may be dull and translucent. [4]
The mineral is biaxial (+), with refractive indices Nx ~ 1.54, Ny ~ 1.56 and Nz ~ 1.58 to 1.60.
For the three main localities the reported values are:
It is mildly pleochroic, with X colorless, Y colorless to pale brown or green and Z generally reddish brown. No fluorescence has been observed. [4]
Cleavage is good on a plane containing the b and c crystal axes, parallel to the layers within the structure, and twinning is common. [5] [7]
Fracture is uneven to conchoidal (shell-like) and the mineral is brittle; [7] it is quite light, with specific gravity 2.465, [3] [6] which is similar to that of quartz.
The type locality is Tuperssuatsiat Bay, Tunugdliarfik Firth (Eriksfjord), Ilimaussaq complex, Narsaq, Kitaa (West Greenland) Province, Greenland, [6] and type material is conserved at the University of Copenhagen, Copenhagen, Denmark, and at the National Museum of Natural History, Washington DC, US, reference number 162402. [7]
Analcime (; from Ancient Greek ἀνάλκιμος (análkimos) 'not strong') or analcite is a white, gray, or colorless tectosilicate mineral. Analcime consists of hydrated sodium aluminium silicate in cubic crystalline form. Its chemical formula is NaAlSi2O6·H2O. Minor amounts of potassium and calcium substitute for sodium. A silver-bearing synthetic variety also exists (Ag-analcite). Analcime is usually classified as a zeolite mineral, but structurally and chemically it is more similar to the feldspathoids. Analcime is not classified as an isometric crystal, as although the crystal structure appears to be isometric, it is usually off only by a fraction of an angle. However, there are truly isometric samples of the mineral, which makes its classification even more difficult. Due to the differences between the samples being too slight, there's no merit from having multiple species names, so as a result analcime is a common example for minerals occurring in multiple crystal systems and space groups. It was first described by French geologist Déodat de Dolomieu, who called it zéolithe dure, meaning hard zeolite. It was found in lava in Cyclops, Italy. The mineral is IMA approved, and had been grandfathered, meaning the name analcime is believed to refer to a valid species til this day.
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.
Nepheline syenite is a holocrystalline plutonic rock that consists largely of nepheline and alkali feldspar. The rocks are mostly pale colored, grey or pink, and in general appearance they are not unlike granites, but dark green varieties are also known. Phonolite is the fine-grained extrusive equivalent.
Sodalite is a tectosilicate mineral with the formula Na
8(Al
6Si
6O
24)Cl
2, with royal blue varieties widely used as an ornamental gemstone. Although massive sodalite samples are opaque, crystals are usually transparent to translucent. Sodalite is a member of the sodalite group with hauyne, nosean, lazurite and tugtupite.
Stilbite is the name of a series of tectosilicate minerals of the zeolite group. Prior to 1997, stilbite was recognized as a mineral species, but a reclassification in 1997 by the International Mineralogical Association changed it to a series name, with the mineral species being named:
Natrolite is a tectosilicate mineral species belonging to the zeolite group. It is a hydrated sodium and aluminium silicate with the formula Na2Al2Si3O10·2H2O. The type locality is Hohentwiel, Hegau, Germany.
Scolecite is a tectosilicate mineral belonging to the zeolite group; it is a hydrated calcium silicate, CaAl2Si3O10·3H2O. Only minor amounts of sodium and traces of potassium substitute for calcium. There is an absence of barium, strontium, iron and magnesium. Scolecite is isostructural (having the same structure) with the sodium-calcium zeolite mesolite and the sodium zeolite natrolite, but it does not form a continuous chemical series with either of them. It was described in 1813, and named from the Greek word, σκώληξ (sko-lecks) = "worm" because of its reaction to the blowpipe flame.
Villiaumite is a rare halide mineral composed of sodium fluoride, NaF. It is very soluble in water and some specimens fluoresce under long and short wave ultraviolet light. It has a Mohs hardness of 2.5 and is usually red, pink, or orange in color. It is toxic to humans.
Eudialyte, whose name derives from the Greek phrase Εὖ διάλυτος, eu dialytos, meaning "well decomposable", is a somewhat rare, nine member ring cyclosilicate mineral, which forms in alkaline igneous rocks, such as nepheline syenites. Its name alludes to its ready solubility in acid.
Gmelinite-Na is one of the rarer zeolites but the most common member of the gmelinite series, gmelinite-Ca, gmelinite-K and gmelinite-Na. It is closely related to the very similar mineral chabazite. Gmelinite was named as a single species in 1825 after Christian Gottlob Gmelin (1792–1860) professor of chemistry and mineralogist from Tübingen, Germany, and in 1997 it was raised to the status of a series.
Gmelinite-Na has been synthesised from Na-bearing aluminosilicate gels. The naturally occurring mineral forms striking crystals, shallow, six sided double pyramids, which can be colorless, white, pale yellow, greenish, orange, pink, and red. They have been compared to an angular flying saucer.
Todorokite is a complex hydrous manganese oxide mineral with generic chemical formula (Na,Ca,K,Ba,Sr)
1-x(Mn,Mg,Al)
6O
12·3-4H
2O. It was named in 1934 for the type locality, the Todoroki mine, Hokkaido, Japan. It belongs to the prismatic class 2/m of the monoclinic crystal system, but the angle β between the a and c axes is close to 90°, making it seem orthorhombic. It is a brown to black mineral which occurs in massive or tuberose forms. It is quite soft with a Mohs hardness of 1.5, and a specific gravity of 3.49 – 3.82. It is a component of deep ocean basin manganese nodules.
Normandite is a brittle orange brown sorosilicate mineral discovered in 1997 by Charles Normand, of Montreal. Normandite occurs in Khibiny Massif, Kola, Russia; in Poudrette quarry, Mont-Saint-Hilaire, Quebec and Tenerife, Canary Islands. It is found in nepheline syenite and in miarolitic cavities in nepheline syenite, associated with nepheline, albite, microcline, aegirine, natrolite, catapleiite, kupletskite, eudialyte, cancrinite, villiaumite, rinkite, and donnayite-(Y).
Yuksporite is a rare inosilicate mineral with double width, unbranched chains, and the complicated chemical formula K4(Ca,Na)14Sr2Mn(Ti,Nb)4(O,OH)4(Si6O17)2(Si2O7)3(H2O,OH)3. It contains the relatively rare elements strontium, titanium and niobium, as well as the commoner metallic elements potassium, calcium, sodium and manganese. As with all silicates, it contains groups of linked silicon and oxygen atoms, as well as some associated water molecules.
Gonnardite is a comparatively rare, fibrous zeolite, natrolite subgroup. Older papers claim that a complete solid solution exists between tetranatrolite and gonnardite, but tetranatrolite was discredited as a separate species in 1999. A series, based on the disorder of the silicon-aluminum in the framework, appears to exist between Na-rich gonnardite and natrolite, Na2(Si3Al2)O10·2H2O.
Lavendulan is an uncommon copper arsenate mineral, known for its characteristic intense electric blue colour. It belongs to the lavendulan group, which has four members:
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.
Vlasovite is a rare inosilicate (chain silicate) mineral with sodium and zirconium, with the chemical formula Na2ZrSi4O11. It was discovered in 1961 at Vavnbed Mountain in the Lovozero Massif, in the Northern Region of Russia. The researchers who first identified it, R P Tikhonenkova and M E Kazakova, named it for Kuzma Aleksevich Vlasov (1905–1964), a Russian mineralogist and geochemist who studied the Lovozero massif, and who was the founder of the Institute of Mineralogy, Geochemistry, and Crystal Chemistry of Rare Elements, Moscow, Russia.
Serandite is a mineral with formula Na(Mn2+,Ca)2Si3O8(OH). The mineral was discovered in Guinea in 1931 and named for J. M. Sérand. Serandite is generally red, brown, black or colorless. The correct name lacks an accent.
Leifite is a rare tectosilicate. Tectosilicates are built on a framework of tetrahedra with silicon or aluminium at the centre and oxygen at the vertices; they include feldspars and zeolites, but leifite does not belong in either of these categories. It is a member of the leifite group, which includes telyushenkoite (Cs,Na,K)Na6(Be2Al3Si15O39) and eirikite KNa6Be2(Si15Al3)O39F2). Leifite was discovered in 1915, and named after Leif Ericson who was a Norse explorer who lived around 1000 AD, and was probably the first European to land in North America, nearly 500 years before Christopher Columbus. Eirikite was named in 2007 after Eirik Raude, or Erik the Red, (950–1003), who discovered Greenland and who was the father of Leif Ericson. The third mineral in the group, telyushenkoite, was discovered in 2001. It was not named after any of Leif Ericson's family members, but after a professor of geology in Turkmenistan.
Taseqite is a rare mineral of the eudialyte group, with chemical formula Na12Sr3Ca6Fe3Zr3NbSiO(Si9O27)2(Si3O9)2(O,OH,H2O)3Cl2. The formula given is derived from the original one and shows a separate silicon at the M4 site, basing on the nomenclature of the eudialyte group. Taseqite, khomyakovite and manganokhomyakovite are three group representatives with species-defining strontium, although many other members display strontium diadochy. Both strontium (N4Sr) and niobium (M3Nb) are essential in the crystal structure of taseqite. When compared to khomyakovite, taseqite differs in niobium- and chlorine-dominance.