Jerrygibbsite | |
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General | |
Category | Nesosilicates |
Formula (repeating unit) | (Mn,Zn)9(SiO4)4(OH)2 |
IMA symbol | Jgb [1] |
Strunz classification | 9.AF.70 |
Crystal system | Orthorhombic |
Crystal class | Pyramidal (mm2) H-M Symbol: (mm2) |
Space group | Pbn21 |
Unit cell | a = 4.85, b = 10.7 c = 28.17 [Å]; Z = 4 |
Identification | |
Color | Violet-pink, with a brownish tinge |
Crystal habit | Interlocking anhedral crystals |
Cleavage | Imperfect on {001} |
Mohs scale hardness | 5.5 |
Luster | Vitreous |
Streak | Light pink |
Diaphaneity | Alternating transparent and translucent lamellae |
Specific gravity | 4.00 |
Optical properties | Biaxial (-) |
Refractive index | nα = 1.772 nβ = 1.783 nγ = 1.789 |
Birefringence | δ = 0.017 |
2V angle | Measured: 72° |
References | [2] [3] |
Jerrygibbsite is a rare silicate mineral with the chemical formula (Mn,Zn)9(SiO4)4(OH)2. Jerrygibbsite was originally discovered by Pete J. Dunn in 1984, who named it after mineralogist Gerald V. Gibbs (born 1929). It has only been reported from the type locality of Franklin Furnace, New Jersey, United States, and in Namibia's Otjozondjupa region. Jerrygibbsite is member of the leucophoenite family of the humite group. It is always found with these two minerals. It is a dimorph of sonolite.
The mineral jerrygibbsite was discovered in 1984 by Pete Dunn while conducting an X-ray spectrographic analysis of a sample previously assumed to be leucophoenicite. [4] All samples found of jerrygibbsite are impure. All are incorporated within leucophoenicite, many by mixed layering, and tend to be found with many manganese humites such as sonolite. Physical properties are similar to those of leucophoenicite and sonolite, including hardness, coloring, and density.
The formula for jerrygibbsite is ((Mn,Zn)9(SiO4)4(OH)2, although it often contains impurities of iron, magnesium, calcium or water. [5] The idealized formula is Mn9(SiO4)4(OH)2 which is the same ideal formula as sonolite, a member of the humite group. [4] Jerrygibbsite has been found to be dimorphous with sonolite. [4]
Jerrygibbsite has been found only in the Franklin Furnace mine in Franklin, New Jersey, and in the Kombat Mines in Namibia. [5] [4] Most of the minerals in the humite group have been found only here, as well as leucophoenicite. Jerrygibbsite has been found to occur in contact with willemite, zincite, and sonolite in an uncommon assemblage. [4] Jerrygibbsite typically occurs as a massive mineral in interlocking anhedral crystals, up to 0.5 mm × 2.0 mm, which display a typical metamorphic texture. [4] Subsequent finds from the Namibia mines were of two different textures.
Jerrygibbsite, in pure form, is a violet-pink mineral with a light pink streak. It has a calculated density of 4.045 g/cm3, and a tested density of 4.00 g/cm3, agreeing favorably, since measurements used to test density have few significant figures. It has a hardness of about 5.5, that of a knife blade. [4] The general luster is vitreous, or shiny. Crystals are generally transparent to translucent. Crystals are not luminescent or fluorescent. [4] Jerrygibbsite forms orthorhombic crystals with an imperfect cleavage along the {001} plane, which can be seen by opaque lamellae alternating with the transparent jerrygibbsite. Optically, jerrygibbsite is negative biaxial with 2V = 72˚ and a maximum birefringence of 0.017. [4] In thin section, jerrygibbsite appears light pink. The crystal structure described by Kato is the equivalent of a unit-cell-twinned sonolite in which the cells are related by a b/4 glide plane. [4]
Dioptase is an intense emerald-green to bluish-green copper cyclosilicate mineral. It is transparent to translucent. Its luster is vitreous to sub-adamantine. Its formula is Cu6Si6O18·6H2O (also reported as CuSiO2(OH)2). It has a hardness of 5, the same as tooth enamel. Its specific gravity is 3.28–3.35, and it has two perfect and one very good cleavage directions. Additionally, dioptase is very fragile, and specimens must be handled with great care. It is a trigonal mineral, forming 6-sided crystals that are terminated by rhombohedra.
Hardystonite is a rare calcium zinc silicate mineral first described from the Franklin, New Jersey, U.S. zinc deposits. It often contains lead, which was detrimental to the zinc smelting process, so it was not a useful ore mineral. Like many of the famous Franklin minerals, hardystonite responds to short wave ultraviolet light, emitting a fluorescence from dark purple to bright violet blue. In daylight, it is white to gray to light pink in color, sometimes with a vitreous or greasy luster. It is very rarely found as well formed crystals, and these are usually rectangular in appearance and rock-locked.
Clinohumite is an uncommon member of the humite group, a magnesium silicate according to the chemical formula (Mg, Fe)9(SiO4)4(F,OH)2. The formula can be thought of as four olivine (Mg2SiO4), plus one brucite (Mg(OH)2). Indeed, the mineral is essentially a hydrated olivine and occurs in altered ultramafic rocks and carbonatites. Most commonly found as tiny indistinct grains, large euhedral clinohumite crystals are sought by collectors and occasionally fashioned into bright, yellow-orange gemstones. Only two sources of gem-quality material are known: the Pamir Mountains of Tajikistan, and the Taymyr region of northern Siberia. It is one of two humite group minerals that have been cut into gems, the other being the much more common chondrodite.
Todorokite is a rare complex hydrous manganese oxide mineral with the 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.
Chondrodite is a nesosilicate mineral with formula (Mg,Fe)
5(SiO
4)
2(F,OH,O)
2. Although it is a fairly rare mineral, it is the most frequently encountered member of the humite group of minerals. It is formed in hydrothermal deposits from locally metamorphosed dolomite. It is also found associated with skarn and serpentinite. It was discovered in 1817 at Pargas in Finland, and named from the Greek for "granule", which is a common habit for this mineral.
Geigerite is a mineral, a complex hydrous manganese arsenate with formula: Mn5(AsO3OH)2(AsO4)2·10H2O. It forms triclinic pinacoidal, vitreous, colorless to red to brown crystals. It has a Mohs hardness of 3 and a specific gravity of 3.05.
Seamanite, named for discoverer Arthur E. Seaman, is a rare manganese boron phosphate mineral with formula Mn3[B(OH)4](PO4)(OH)2. The yellow to pink mineral occurs as small, needle-shaped crystals. It was first discovered in 1917 from a mine in Iron County, Michigan, United States and identified in 1930. As of 2012, seamanite is known from four sites in Michigan and South Australia.
Jarosewichite is a rare manganese arsenate mineral with formula: Mn2+3Mn3+(AsO4)(OH)6. It was first described in Franklin, New Jersey which is its only reported occurrence. Its chemical composition and structure are similar to chlorophoenicite. This mineral is orthorhombic with 2/m2/m2/m point group. Its crystals are prismatic or barrel-shaped. The color of jarosewichite is dark red to black. It has subvitreous luster of fracture surfaces and reddish-orange streak. This mineral occurs with flinkite, franklinite, andradite and cahnite.
Reinerite is a rare arsenite (arsenate(III)) mineral with chemical formula Zn3(AsO3)2. It crystallizes in the orthorhombic crystal system.
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
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.
The humite group is a group of nesosilicates with the general formula An(SiO4)m(F,OH)2.
Warikahnite is a rare zinc arsenate mineral of the triclinic crystal system with Hermann- Mauguin notation 1, belonging to the space group P1. It occurs in the Tsumeb mine in Namibia on corroded tennantite in the second oxidation zone under hydrothermal conditions in a dolomite-hosted polymetallic ore deposit. It is associated with adamite, stranskiite, koritnigite, claudetite, tsumcorite, and ludlockite. The origin of discovery was in a dolosmite ore formation within an oxidized hydrothermal zone, in the E9 pillar, 31st level of the Tsumeb Mine in Namibia, Southwest Africa. It has also been found at Lavrion, Greece and Plaka, Greece as microscopic white needles.
Whiteite is a rare hydrated phosphate mineral, with hydroxyl
Pimelite was discredited as a mineral species by the International Mineralogical Association (IMA) in 2006, in an article which suggests that “pimelite” specimens are probably willemseite, or kerolite. This was a mass discreditation, and not based on any re-examination of the type material. Nevertheless, a considerable number of papers have been written, verifying that pimelite is a nickel-dominant smectite. It is always possible to redefine a mineral wrongly discredited.
Leucophoenicite is a mineral with formula Mn7(SiO4)3(OH)2. Generally brown to red or pink in color, the mineral gets its name from the Greek words meaning "pale purple-red". Leucophoenicite was discovered in New Jersey, US and identified as a new mineral in 1899.
Ruizite is a sorosilicate mineral with formula Ca2Mn2Si4O11(OH)4·2H2O. It was discovered at the Christmas mine in Christmas, Arizona, and described in 1977. The mineral is named for discoverer Joe Ana Ruiz.
Franklinphilite is a phyllosilicate of the stilpnomelane group. Known from only two localities It was found exclusively from the Franklin and Sterling Hill mines in Franklin, Sussex County, New Jersey. until 2013, when a locality in Wales was confirmed
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.
Mammothite is a mineral found in the Mammoth mine in Tiger, Arizona and also in Laurium, Attika, Greece. This mineral was named in 1985 by Donald R. Peacor, Pete J. Dunn, G. Schnorrer-Köhler, and Richard A. Bideaux, for the Mammoth vein (one of the two main veins in the mine) and the town of Mammoth, Arizona, which was named for the mine. The mammothite that is found in Arizona exist as euhedral crystals imbedded in micro granular, white colored anglesite with a saccharoidal texture. The associated minerals include phosgenite, wulfenite, leadhillite and caledonite. In Greece, the mammothite exists as small euhedral crystals and also as microscopic rock cavities lined with projecting crystals within the slags. The associated minerals here are cerussite, phosgenite and matlockite. The ideal chemical formula for mammothite is Pb6Cu4AlSb5+O2(OH)16Cl4(SO4)2.