Minerals in space group 160

thumb|upright=1.3|Main tourmaline producing countries

Molybdenite is a mineral of molybdenum disulfide, MoS2. Similar in appearance and feel to graphite, molybdenite has a lubricating effect that is a consequence of its layered structure. The atomic structure consists of a sheet of molybdenum atoms sandwiched between sheets of sulfur atoms. The Mo-S bonds are strong, but the interaction between the sulfur atoms at the top and bottom of separate sandwich-like tri-layers is weak, resulting in easy slippage as well as cleavage planes. Molybdenite crystallizes in the hexagonal crystal system as the common polytype 2H and also in the trigonal system a

Millerite or nickel blende is a nickel sulfide mineral, NiS. It is brassy in colour and has an acicular habit, often forming radiating masses and furry aggregates. It can be distinguished from pentlandite by crystal habit, its duller colour, and general lack of association with pyrite or pyrrhotite.

Elbaite, a sodium, lithium, aluminium boro-silicate, with the chemical composition Na(Li1.5Al1.5)Al6Si6O18(BO3)3(OH)4, is a mineral species belonging to the six-member ring cyclosilicate tourmaline group.

Corkite is a phosphate mineral in the beudantite subgroup of the alunite group. Corkite is the phosphate analogue of beudantite and with it, a complete solid solution range exists. Corkite will also form a solid solution with kintoreite.

Fluor-uvite is a tourmaline mineral with the chemical formula CaMg3(Al5Mg)(Si6O18)(BO3)3(OH)3F. It is a rare mineral that is found in calcium rich contact metamorphic rocks with increased amounts of boron. Uvite is trigonal hexagonal, which means that it has three equal length axes at 120 degrees, all perpendicular to its fourth axis which has a different length. Uvite is part of the space group 3m. Uvite's hardness has been measured to be 7.5 on the Mohs hardness scale. The color of uvite widely varies, depending on the sample, but is mostly deep green or brown. In regard to uvite's optical p

Fluor-buergerite, originally named buergerite, is a mineral species belonging to the tourmaline group. It was first described for an occurrence in rhyolitic cavities near Mexquitic, San Luis Potosi, Mexico. It was approved as a mineral in 1966 by the IMA and named in honor of Martin J. Buerger (1903–1986), professor of mineralogy at the Massachusetts Institute of Technology. It has also been reported from Minas Gerais, Brazil, and the Central Bohemia Region of the Czech Republic.

Gratonite is a lead-arsenic sulfosalt mineral, with the chemical composition Pb9As4S15. It is considered a low-temperature dimorph of jordanite. Gratonite was discovered in 1939 at the Excelsior Mine, Cerro de Pasco, Peru. It is named in honor of geologist L. C. Graton (1880–1970), who had a long-standing association with the Cerro de Pasco mines. The other location where it is found is the Rio Tinto mine, Minas de Riotinto (Huelva), Spain. The crystals are very similar to those from Cerro de Pasco.

Povondraite is a rare silicate mineral from the tourmaline group with formula: NaFe3+3(Fe3+4,Mg2)(BO3)3Si6O18(OH)3O. It is a dark brown to black nearly opaque mineral with a resinous to splendent luster. It crystallizes in the trigonal crystal system as equant, distorted prisms with trigonal pyramid terminations.

Khomyakovite is an exceedingly rare mineral of the eudialyte group, with formula . The original formula was extended to show the presence of both the cyclic silicate groups and M4-site silicon, according to the nomenclature of the eudialyte group. Some niobium substitutes for tungsten in khomyakovite. Khomyakovite is an iron-analogue of manganokhomyakovite, the second mineral being a bit more common. The two minerals are the only group representatives, beside taseqite, with species-defining strontium, although many other members display strontium diadochy. Khomyakovite is the third eudialyte-g

Ikranite is a member of the eudialyte group, named after the Shubinov Institute of Crystallography of the Russian Academy of Sciences. It is a cyclosilicate mineral that shows trigonal symmetry with the space group R3m, and is often seen with a pseudo-hexagonal habit. Ikranite appears as translucent and ranges in color from yellow to a brownish yellow. This mineral ranks a 5 on Mohs scale of mineral hardness, though it is considered brittle, exhibiting conchoidal fracture when broken.

Changbaiite (PbNb2O6) is a member of the oxide mineral class in which the mineral contains oxygen which is grouped along with one or two metal ion. Changbaiite is classified as a multiple Oxide XY2O6 and it generally has an ionic bond. Furthermore, it is also orthorhombic at a temperature of 25 °C and it changes to orthorhombic-tetragonal at 570 °C.

Fluor-liddicoatite is a rare member of the tourmaline group of minerals, elbaite subgroup, and the theoretical calcium endmember of the elbaite-fluor-liddicoatite series; the pure end-member has not yet been found in nature. Fluor-liddicoatite is indistinguishable from elbaite by X-ray diffraction techniques. It forms a series with elbaite and probably also with olenite. Liddiocoatite is currently a non-approved mineral name, but Aurisicchio et al. (1999) and Breaks et al. (2008) found OH-dominant species. Formulae are Fluor-liddicoatite Ca(Li2Al)Al6(BO3)3Si6O18(OH)3F Elbaite Na(Al1.5Li1.5)A

Lucchesiite is a new member of tourmaline-group of minerals. Lucchesiite has the formula CaFe3Al6(Si6O18)(BO3)3(OH)3O. It is the calcium and oxygen-analogue of schorl. It has two co-type localizations, one in Czech Republic and the other in Sri Lanka. As the other members of the tourmaline group, it is trigonal.

Zirsilite-(Ce) is a very rare mineral of the eudialyte group, with formula . The original formula was extended to show the presence of cyclic silicate groups and the presence of silicon at the M4 site, according to the nomenclature of the eudialyte group. Zirsilite-(Ce) differs from carbokentbrooksite in cerium-dominance over sodium only. Both minerals are intimately associated. The only other currently known representative of the eudialyte group having rare earth elements (in particular cerium, as suggested by the "-Ce)" Levinson suffix in the name) in dominance is johnsenite-(Ce).

Geerite is a copper sulfide mineral with the chemical formula Cu8S5. The mineral is named after the original collector, Adam Geer, of Utica, New York, US.

Rastsveatevite is a rare mineral of the eudialyte group with the chemical formula . Its structure is modular. It is only the third member of the group after andrianovite and davinciite with essential (site-dominating) potassium. Potassium and sodium enter both N4 and M2 sites. The mineral is named after Russian crystallographer Ramiza K. Rastsvetaeva.

Andrianovite is a very rare mineral of the eudialyte group, with formula Na12(K,Sr,Ce)6Ca6(Mn,Fe)3Zr3NbSi(Si3O9)2(Si9O27)2O(O,H2O,OH)5. The original formula was extended to show the presence of cyclic silicate groups and silicon at the M4 site, according to the nomenclature of eudialyte group. Andrianovite is unique among the eudialyte group in being potassium-rich (other eudialyte-group species with essential K are davinciite and rastsvetaevite). It is regarded as potassium analogue of kentbrooksite, but it also differs from it in being oxygen-dominant rather than fluorine-dominant. Also, the

Georgbarsanovite is a very rare mineral of the eudialyte group, formerly known under unaccepted name as barsanovite, with formula . The original formula was extended to show the presence of cyclic silicate groups and the domination of silicon at the M4 site. "REE", standing for rare earth elements, is dominated by cerium. Georgbarsanovite is characterized in dominance of manganese at the N4 site. It also differs from most other accepted group representatives in its colour. The mineral was found in nepheline pegmatite near Petrelius River, Khibiny massif, Kola Peninsula, Russia. It is named aft

Feklichevite is a rare mineral of the eudialyte group with the formula Na11Ca9(Fe3+,Fe2+)2Zr3NbSi(Si3O9)2(Si9O27)2. The original formula was extended to show the presence of cyclic silicate groups and presence of silicon at the M4 site, according to the nomenclature of eudialyte group. When compared to other minerals of the group, feklichevite characterizes in the presence of ferric iron (thus similar to ikranite, mogovidite and fengchengite) and dominance of calcium at the N4 site. Calcium is ordered in the structure and is also present at the M1 site. Other iron-bearing minerals of the group

Manganoeudialyte is an moderately rare mineral of the eudialyte group, with formula Na14Ca6Mn3Zr3Si2[Si24O72(OH)2]Cl2·4H2O. The formula given is one of the forms that can be given, based on the originally reported one, and shows dominance of silicon at both the M3 and M4 sites. As suggested by its name, it is the manganese-analogue of eudialyte.

Ferrokentbrooksite is a moderately rare mineral of the eudialyte group, with formula . The original formula was extended form to show the presence of cyclic silicate groups and presence of silicon at the M4 site, according to the nomenclature of eudialyte group. As suggested by its name, it is the (ferrous) iron analogue of kentbrooksite. When compared to the latter, it is also chlorine-dominant instead of being fluorine-dominant. The original (holotype) material is also relatively enriched in rare earth elements, including cerium and yttrium.

Dualite is a very rare and complex mineral of the eudialyte group, its complexity being expressed in its formula . The formula is simplified as it does not show the presence of cyclic silicate groups. The name of the mineral comes from its dual nature: zircono- and titanosilicate at once. Dualite has two modules in its structure: alluaivite one and eudialyte one. After alluaivite and labyrinthite it stands for third representative of the eudialyte group with essential titanium.

Cervandonite is a rare arsenosilicate mineral. It has a chemical formula or . It has a monoclinic crustal structure with supercell (Z=6), the crystal structure was established as a trigonal subcell, with space group R3m and a = 6.508(1)Ǻ, c = 18.520(3) Ǻ, V 679.4(2) Ǻ3, and Z=3. It was first described by Buhler Armbruster in 1988, but it has proven to be problem due to the extreme scarcity of single crystals and its unusual replacement of silicon and arsenic. Cervandonite is named after the location where it was first described, Pizzo Cervandone (Scherbadung), Italy in the Central Alps.

Davinciite is a very rare mineral of the eudialyte group, with the simplified formula Na12K3Ca6Fe32+Zr3(Si26O73OH)Cl2. The formula given does not show the presence of cyclic silicate groups. The mineral was named after Leonardo da Vinci to refer to the atypical geometrical forms he tended to use, compared by the authors of the mineral description to the atypical (not ideally centrosymmetrical) geometry of the Davinciite structure. The other quite atypical feature of Davinciite is its lavender colour, while the typical eudialyte is rather pink or red.

Kentbrooksite is a moderately rare mineral of the eudialyte group, with chemical formula . This extended formula shows the presence of cyclic silicate groups and dominance of Si at the M4 site, according to the nomenclature of the eudialyte group. The characteristic features of kentbrooksite, that make it different from eudialyte are: (1) dominancy of fluorine (the only currently known example among the whole group), (2) dominancy of manganese, and (3) dominancy of niobium. Trace hafnium and magnesium are also reported. Kentbrooksite is relatively common when compared to most other species of

Manganokhomyakovite is a very rare mineral of the eudialyte group, with the chemical formula . This formula is in extended form (based on the original one), to show the presence of cyclic silicate groups and domination of silicon at the M4 site, basing on the nomenclature of the eudialyte group. Some niobium substitutes for tungsten in khomyakovite. As suggested by its name, manganokhomyakovite is a manganese-analogue of khomyakovite, the latter being more rare. The two minerals are the only group representatives, beside taseqite, with species-defining strontium, although many other members di