Celestine (the IMA-accepted name) or celestite is a mineral consisting of strontium sulfate (SrSO4). The mineral is named for its occasional delicate blue color. Celestine and the carbonate mineral strontianite are the principal sources of the element strontium, commonly used in fireworks and in various metal alloys.
Weloganite is a rare carbonate mineral with formula: Na2(Sr,Ca)3Zr(CO3)6·3H2O. It was discovered by Canadian government mineralogist Ann P. Sabina in 1967 and named for Canadian geologist Sir William Edmond Logan (1798–1875). It was first discovered in Francon Quarry, Montreal, Quebec, Canada and has only been reported from a few localities worldwide.
Creedite is a calcium aluminium sulfate fluoro hydroxide mineral with formula: Ca3Al2SO4(F,OH)10·2(H2O). Creedite forms colorless to white to purple monoclinic prismatic crystals. It often occurs as acicular radiating sprays of fine prisms. It is translucent to transparent with indices of refraction of nα = 1.461 nβ = 1.478 nγ = 1.485. It has a Mohs hardness of 3.5 to 4 and a specific gravity of 2.7.
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.
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.
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.
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.
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.
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.
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).
Strontium carbonate (SrCO3) is the carbonate salt of strontium that has the appearance of a white or grey powder. It occurs in nature as the mineral strontianite.
Tuperssuatsiaite is a rare clay mineral found in Greenland, Namibia and Brazil. It is a hydrated phyllosilicate of sodium and iron.
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.
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.
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.
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.
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.
Raygrantite is a mineral that was first discovered in Big Horn Mountains, Maricopa County, Arizona, USA. More specifically, it is located in the evening star mine, which is a Cu, V, Pb, Ag, Au, and W mine. Raygrantite is a member of the iranite mineral group, which consists of Hemihedrite, Iranite, and Raygrantite. This mineral received its name in honor of Dr. Raymond W. Grant, a retired professor who primarily focused on the minerals of Arizona. The typical crystal structure of this mineral is bladed with parallel striations to the C axis. It's ideal chemical formula is Pb10Zn(SO4)6(SiO4)2(OH)2. Finally, the IMA (International Mineralogical Association) approved this mineral in 2013, and the first publication regarding this mineral was put forth in 2017.
