Greenwoodite | |
---|---|
General | |
Category | Nesosilicate |
Formula (repeating unit) | Ba 2-x(V 3+ OH)x V 9(Fe 3+, Fe 2+)2 Si 2 O 22 |
IMA symbol | Gwd [1] |
Strunz classification | 9.AH.55 |
Crystal system | Trigonal |
Crystal class | 3m (3/2m) - Hexagonal Scalenohedral (same H-M symbol) |
Space group | P3m1 |
Unit cell | a = 5.750 Å, b = 5.750 Å c = 14.459 Å; α=90.00° β=90.00°, γ=120.00° |
Identification | |
Color | Black |
Crystal habit | Semi-Prismatic to Tabular Crystals |
Cleavage | Perfect on {001} |
Tenacity | Brittle |
Mohs scale hardness | 5 |
Luster | Sub-Metallic, Dull |
Diaphaneity | Transparent |
Specific gravity | 4.81 (Calculated) |
Density | 4.81 g/cm3 |
References | [2] [4] |
Greenwoodite is the second mineral discovered in the Wigwam deposit of southeastern British Columbia, Canada. It is compositionally and structurally distinct, but compositionally related to zoltaiite, the first new mineral described from this locality. The name is in honor of Hugh J. Greenwood, retired professor and former head of the Geological Sciences Department at the University of British Columbia, Vancouver, British Columbia, Canada. Grain size, polyhedral grain boundaries, and the general lack of secondary mineralization indicate that greenwoodite is part of a prograde metamorphic assemblage. The ideal chemical formula for greenwoodite is Ba 2-x(V 3+ OH)x V 9(Fe 3+, Fe 2+)2 Si 2 O 22. [2] [3]
Greenwoodite is part of the prograde assemblage in a greenschist facies metamorphosed Mississippi-Valley type base-metal deposit. [4] Greenwoodite is found as part of a suite of three minerals: greenwoodite, zoltaiite, and batisivite. [2] All three minerals are found together in the Wigwam Deposit of British Columbia. All three of these minerals occur as trace phases within an assemblage of quartz, celsian, apatite, sphalerite, pyrrhotite, galena, and pyrite. Greenwoodite occurs as small, disseminated semi-prismatic to tabular grains. [2] Greenwoodite occurs as small, disseminated semi-prismatic to tabular grains. Irregular grains intergrown with other phases are common as well. [2] Grains of greenwoodite can range from areas of 800 microns to 20,000 microns. The grains of greenwoodite can be found isolated, but are generally found in groups of 2-10 closely-spaced groups. [2]
Greenwoodite is a black and/or opaque mineral that has a sub-metallic/dull luster. On the Mohs Scale of Mineral Hardness, greenwoodite is a 5. Greenwoodite has one perfect plane of cleavage which is found on the {001} plane. The tenacity of Greenwoodite is brittle meaning it breaks or shatters very easily. The calculated density of greenwoodite is 4.81 g/cm3. [2] [3] [4] `
In reflected light, greenwoodite has a low reflectance (similar to that of sphalerite), gray color with a weak brownish tint, no internal reflections, and distinct bireflectance, pleochroism, and anisotropy with straight extinction relative to its cleavage direction. [2]
The empirical formula for greenwoodite is Ba0.60(V3+OH)0.40(V3+8.33, Cr0.33, Ti0.13, Al0.13, Mn3+0.02)Σ9(Fe3+1.08, Fe2+0.60, Zn0.22, Al0.06, Mg0.04)Σ2(Si1.72, Fe3+0.28)Σ2O22
Oxide | wt% |
---|---|
MgO | 0.12 |
Al2O3 | 0.91 |
SiO2 | 8.63 |
TiO2 | 1.05 |
V2O3 | 58.03 |
Cr2O3 | 1.42 |
MnO | 0.11 |
FeO | [3.72] |
Fe2O3 | [9.1] |
ZnO | 1.52 |
BaO | 15.13 |
H2O | [0.62] |
Total | 100.36 |
Greenwoodite is part of the Trigonal System with a Space Group of P3m1. The unit cell dimensions are a = 5.750 Å, b = 5.750 Å c = 14.459 Å; α=90.00° β=90.00°, γ=120.00°. [3] The calculated X-Ray Powder pattern is 2.925 (100), 2.875 (38), 2.469 (35), 1.438 (35), 2.354 (28), 2.212 (28), 1.669 (26). [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.
Arsenopyrite is an iron arsenic sulfide (FeAsS). It is a hard metallic, opaque, steel grey to silver white mineral with a relatively high specific gravity of 6.1. When dissolved in nitric acid, it releases elemental sulfur. When arsenopyrite is heated, it produces sulfur and arsenic vapor. With 46% arsenic content, arsenopyrite, along with orpiment, is a principal ore of arsenic. When deposits of arsenopyrite become exposed to the atmosphere, the mineral slowly converts into iron arsenates. Arsenopyrite is generally an acid-consuming sulfide mineral, unlike iron pyrite which can lead to acid mine drainage.
Sphalerite is a sulfide mineral with the chemical formula (Zn,Fe)S. It is the most important ore of zinc. Sphalerite is found in a variety of deposit types, but it is primarily in sedimentary exhalative, Mississippi-Valley type, and volcanogenic massive sulfide deposits. It is found in association with galena, chalcopyrite, pyrite, calcite, dolomite, quartz, rhodochrosite, and fluorite.
Germanite is a rare copper iron germanium sulfide mineral, Cu26Fe4Ge4S32. It was first discovered in 1922, and named for its germanium content. It is only a minor source of this important semiconductor element, which is mainly derived from the processing of the zinc sulfide mineral sphalerite. Germanite contains gallium, zinc, molybdenum, arsenic, and vanadium as impurities.
Vivianite (Fe2+
Fe2+
2(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.
Pyrrhotite is an iron sulfide mineral with the formula Fe(1-x)S. It is a nonstoichiometric variant of FeS, the mineral known as troilite. Pyrrhotite is also called magnetic pyrite, because the color is similar to pyrite and it is weakly magnetic. The magnetism decreases as the iron content decreases, and troilite is non-magnetic. Pyrrhotite is generally tabular and brassy/bronze in color with a metallic luster. The mineral occurs with mafic igneous rocks like norites, and may form from pyrite during metamorphic processes. Pyrrhotite is associated and mined with other sulfide minerals like pentlandite, pyrite, chalcopyrite, and magnetite, and has been found globally.
Hübnerite or hubnerite is a mineral consisting of manganese tungsten oxide (chemical formula MnWO4). It is the manganese endmember of the manganese–iron wolframite solid solution series. It forms reddish brown to black monoclinic prismatic submetallic crystals. The crystals are typically flattened and occur with fine striations. It has a high specific gravity of 7.15 and a Mohs hardness of 4.5. It is transparent to translucent with perfect cleavage. Refractive index values are nα = 2.170 - 2.200, nβ = 2.220, and nγ = 2.300 - 2.320.
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.
Foliation in geology refers to repetitive layering in metamorphic rocks. Each layer can be as thin as a sheet of paper, or over a meter in thickness. The word comes from the Latin folium, meaning "leaf", and refers to the sheet-like planar structure. It is caused by shearing forces, or differential pressure. The layers form parallel to the direction of the shear, or perpendicular to the direction of higher pressure. Nonfoliated metamorphic rocks are typically formed in the absence of significant differential pressure or shear. Foliation is common in rocks affected by the regional metamorphic compression typical of areas of mountain belt formation.
Digenite is a copper sulfide mineral with formula: Cu9S5. Digenite is a black to dark blue opaque mineral that crystallizes with a trigonal - hexagonal scalenohedral structure. In habit it is usually massive, but does often show pseudo-cubic forms. It has poor to indistinct cleavage and a brittle fracture. It has a Mohs hardness of 2.5 to 3 and a specific gravity of 5.6. It is found in copper sulfide deposits of both primary and supergene occurrences. It is typically associated with and often intergrown with chalcocite, covellite, djurleite, bornite, chalcopyrite and pyrite. The type locality is Sangerhausen, Thuringia, Germany, in copper slate deposits.
Djurleite is a copper sulfide mineral of secondary origin with formula Cu31S16 that crystallizes with monoclinic-prismatic symmetry. It is typically massive in form, but does at times develop thin tabular to prismatic crystals. It occurs with other supergene minerals such as chalcocite, covellite and digenite in the enriched zone of copper orebodies. It is a member of the chalcocite group, and very similar to chalcocite, Cu2S, in its composition and properties, but the two minerals can be distinguished from each other by x-ray powder diffraction. Intergrowths and transformations between djurleite, digenite and chalcocite are common. Many of the reported associations of digenite and djurleite, however, identified by powder diffraction, could be anilite and djurleite, as anilite transforms to digenite during grinding.
Alloclasite is a sulfosalt mineral. It is a member of the arsenopyrite group. Alloclasite crystallizes in the monoclinic system and typically forms as columnar to radiating acicular prismatic clusters. It is an opaque steel-gray to silver-white, with a metallic luster and a black streak. It is brittle with perfect cleavage, a Mohs hardness of 5 and a specific gravity of 5.91–5.95.
Gunningite is one of the minerals in the Kieserite group, with the chemical formula (Zn,Mn2+)SO4·H2O. Its name honours Henry Cecil Gunning (1901–1991) of the Geological Survey of Canada and a professor at the University of British Columbia.
Pabstite is a barium tin titanium silicate mineral that is found in contact metamorphosed limestone. It belongs to the benitoite group of minerals. The chemical formula of pabstite is Ba(Sn,Ti)Si3O9. It is found in Santa Cruz, California. The crystal system of the mineral is hexagonal.
Woodhouseite belongs to the beudantite group AB3(XO4)(SO4)(OH)6 where A = Ba, Ca, Pb or Sr, B = Al or Fe and X = S, As or P. Minerals in this group are isostructural with each other and also with minerals in the crandallite and alunite groups. They crystallise in the rhombohedral system with space group R3m and crystals are usually either tabular {0001} or pseudo-cubic to pseudo-cuboctahedral. Woodhouseite was named after Professor Charles Douglas Woodhouse (1888–1975), an American mineralogist and mineral collector from the University of California, Santa Barbara, US, and one-time General Manager of Champion Sillimanite, Inc.
Awaruite is a naturally occurring alloy of nickel and iron with a composition from Ni2Fe to Ni3Fe.
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.
Scandiobabingtonite was first discovered in the Montecatini granite quarry near Baveno, Italy in a pegmatite cavity. Though found in pegmatites, the crystals of scandiobabingtonite are sub-millimeter sized, and are tabular shaped. Scandiobabingtonite was the sixth naturally occurring mineral discovered with the rare earth element scandium, and grows around babingtonite, with which it is isostructural, hence the namesake. It is also referred to as scandian babingtonite. The ideal chemical formula for scandiobabingtonite is Ca2(Fe2+,Mn)ScSi5O14(OH).
Rockbridgeite is an anhydrous phosphate mineral in the "Rockbridgeite" supergroup with the chemical formula Fe2+Fe3+4(PO4)3(OH)5. It was discovered at the since-shut-down Midvale Mine in Rockbridge County, Virginia, United States. The researcher who first identified it, Clifford Frondel, named it in 1949 for its region of discovery, Rockbridge County.