Santabarbaraite

Last updated
Santabarbaraite
Santabarbaraite-Vivianite-mrz341b.jpg
Santabarbaraite (pseudomorph) after vivianite
General
Category Phosphate minerals
Formula
(repeating unit)
Fe3+3(PO4)2(OH)3·5H2O
IMA symbol Sbb [1]
Strunz classification 8.CE.80
Crystal system Amorphous
Identification
ColorBrown to light brown
Crystal habit Elongated or flattened prisms
Twinning None
Cleavage None, parting along {010} of replaced phase
Fracture Conchoidal
Mohs scale hardnessNot determined
Luster Vitreous to greasy
Streak yellow-umber
Diaphaneity Translucent
Specific gravity 2.24
Optical propertiesisotropic
Refractive index n = 1.659
Other characteristicsPseudomorphism
References [2] [3]

Santabarbaraite is an amorphous ferric hydroxy phosphate mineral hydrate that was discovered in Tuscany, Italy during 2000. [4] It also can be found in Victoria, Australia and Lake Baikal, Siberia. [5]

Contents

This phosphate mineral has a simplified formula Fe3+3(PO4)2(OH)3·5H2O, [4] which is the same formula of another non-amorphous phosphate mineral called allanpringite. [6] Santabarbaraite occurs as pseudomorphic masses after vivianite (Fe2+3(PO4)2·8H2O). In the process, monoclinic vivianite oxidizes to form the amorphous santabarbaraite. [4] Pseudomorphism may be seen in Victoria, Australia, in Wannon Falls (originally a well-known locality for vivianite). It also may be seen at Lake Baikal, Siberia where the oxidized santabarbaraite may be seen as a rim surrounding vivianite due to exposure to air. [5]

Physical properties

Due to pseudomorphism, Santabarbaraite samples show elongated and flattened prism habits. The bulk crystal color is brown to light brown, but appears yellow brown when viewed under an optical microscope. The streak color of the mineral is yellow-umber. [4] Santabarbaraite has a vitreous-to-greasy luster and shows no fluorescence under ultraviolet light. It is translucent and shows good parting along the cleavage of its original mineral vivianite at {010}. Santabarbaraite's density is 2.24 g/cm3. The mineral is isotropic, with refractive index n=1.659. [4]

Taxonomy

Santabarbaraite is named after Santa Barbara, a mining district in Italy where, in 2000, the mineral was discovered and first described. The district name honors the saint of miners, Saint Barbara, [4] which by association, makes santabaraite one of few minerals bearing the name of a woman.

Geologic occurrence

Santabarbaraite occurs in several places. It occurs in the Valderno Superiore lignite-bearing basin in the Santa Barbara mining district, Tuscany, Italy. [4] Santabarbaraite samples may be seen in Victoria, Australia, underlying Pliocene basalt beneath Wannon Falls. [4] It also is found in samples from Lake Baikal, Siberia. [5]

Biological occurrence

Since its discovery in 2000, this mineral hydrate has been found in the teeth of a living organism, the Gumboot chiton. [7] [8]

Related Research Articles

<span class="mw-page-title-main">Limonite</span> Hydrated iron oxide mineral

Limonite is an iron ore consisting of a mixture of hydrated iron(III) oxide-hydroxides in varying composition. The generic formula is frequently written as FeO(OH)·nH2O, although this is not entirely accurate as the ratio of oxide to hydroxide can vary quite widely. Limonite is one of the three principal iron ores, the others being hematite and magnetite, and has been mined for the production of iron since at least 2500 BP.

<span class="mw-page-title-main">Goethite</span> Iron(III) oxide-hydroxide named in honor to the poet Goethe

Goethite is a mineral of the diaspore group, consisting of iron(III) oxide-hydroxide, specifically the "α" polymorph. It is found in soil and other low-temperature environments such as sediment. Goethite has been well known since ancient times for its use as a pigment. Evidence has been found of its use in paint pigment samples taken from the caves of Lascaux in France. It was first described in 1806 based on samples found in the Hollertszug Mine in Herdorf, Germany. The mineral was named after the German polymath and poet Johann Wolfgang von Goethe (1749–1832).

<span class="mw-page-title-main">Vivianite</span>

Vivianite (Fe2+
Fe2+
2
(PO
4
)
2
·8H
2
O
) is a hydrated iron phosphate mineral found in a number of geological environments. Small amounts of manganese Mn2+, magnesium Mg and calcium Ca 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.

<span class="mw-page-title-main">Torbernite</span> Phosphate mineral

Torbernite is a radioactive, hydrated green copper uranyl phosphate mineral, found in granites and other uranium-bearing deposits as a secondary mineral. Its name derives from the Swedish chemist Torbern Bergman (1735–1784), It is also known as chalcolite. Torbernite is isostructural with the related uranium mineral, autunite.

<span class="mw-page-title-main">Thénardite</span> Anhydrous sodium sulfate mineral

Thénardite is an anhydrous sodium sulfate mineral, Na2SO4 which occurs in arid evaporite environments, specifically lakes and playas. It also occurs in dry caves and old mine workings as an efflorescence and as a crusty sublimate deposit around fumaroles. It occurs in volcanic caves on Mount Etna, Italy. It was first described in 1825 for an occurrence in the Espartinas Saltworks, Ciempozuelos, Madrid, Spain and was named for the French chemist, Louis Jacques Thénard (1777–1826).

<span class="mw-page-title-main">Diadochite</span>

Diadochite is a phospho-sulfate mineral. It is a secondary mineral formed by the weathering and hydration of other minerals. Its formula is Fe2(PO4)(SO4)OH·5H2O. Well crystallized forms are referred to as destinezite, which has been given official recognition by the International Mineralogical Association with diadochite being the poorly formed to amorphous variety.

<span class="mw-page-title-main">Iron(II) phosphate</span> Chemical compound

Iron(II) phosphate, also ferrous phosphate, Fe3(PO4)2, is an iron salt of phosphoric acid.

<span class="mw-page-title-main">Iron(III) oxide-hydroxide</span> Chemical compound

Iron(III) oxide-hydroxide or ferric oxyhydroxide is the chemical compound of iron, oxygen, and hydrogen with formula FeO(OH).

<span class="mw-page-title-main">Aheylite</span>

Aheylite is a rare phosphate mineral with formula (Fe2+Zn)Al6[(OH)4|(PO4)2]2·4(H2O). It occurs as pale blue to pale green triclinic crystal masses. Aheylite was made the newest member of the turquoise group in 1984 by International Mineralogical Association Commission on New Minerals and Mineral Names.

<span class="mw-page-title-main">Ikaite</span> Hexahydrated calcium carbonate mineral

Ikaite is the mineral name for the hexahydrate of calcium carbonate, CaCO3·6H2O. Ikaite tends to form very steep or spiky pyramidal crystals, often radially arranged, of varied sizes from thumbnail size aggregates to gigantic salient spurs. It is only found in a metastable state and decomposes rapidly by losing most of its water content once removed from near-freezing water. This "melting mineral" is more commonly known through its pseudomorphs.

<span class="mw-page-title-main">Arthurite</span>

Arthurite is a mineral composed of divalent copper and iron ions in combination with trivalent arsenate, phosphate and sulfate ions with hydrogen and oxygen. Initially discovered by Sir Arthur Russell in 1954 at Hingston Down Consols mine in Calstock, Cornwall, England, arthurite is formed as a resultant mineral in the oxidation region of some copper deposits by the variation of enargite or arsenopyrite. The chemical formula of Arthurite is CuFe23+(AsO4,PO4,SO4)2(O,OH)2•4H2O.

<span class="mw-page-title-main">Anapaite</span> Hydrous phosphate mineral

Anapaite is a calcium–iron phosphate mineral with formula: Ca2Fe2+(PO4)2·4H2O. It is a mineral that typically occurs in cavities in fossil bearing sedimentary rocks. It is also found in phosphate bearing iron ores and rarely in pegmatites. It is commonly found with goethite, siderite and vivianite.

<span class="mw-page-title-main">Hureaulite</span>

Hureaulite is a manganese phosphate with the formula Mn2+5(PO3OH)2(PO4)2·4H2O. It was discovered in 1825 and named in 1826 for the type locality, Les Hureaux, Saint-Sylvestre, Haute-Vienne, Limousin, France. It is sometimes written as huréaulite, but the IMA does not recommend this for English language text.

<span class="mw-page-title-main">Ludlamite</span>

Ludlamite is a rare phosphate mineral with chemical formula (Fe,Mn,Mg)3(PO4)2·4H2O. It was first described in 1877 for an occurrence in Wheal Jane mine in Cornwall, England and named for English mineralogist Henry Ludlam (1824–1880).

<span class="mw-page-title-main">Allanpringite</span> Phosphate mineral

Allanpringite is a phosphate mineral named after Australian mineralogist Allan Pring of the South Australian Museum. Allanpringite is a Fe3+ analogue Al-phosphate mineral wavellite, but it has a different crystal symmetry – monoclinic instead of orthorhombic in wavellite. It forms needle-like crystals, which are always twinned and form parallel bundles up to about 2 mm long. They are often found in association with other iron phosphates in abandoned iron mines.

<span class="mw-page-title-main">Maricite</span>

Maricite or marićite is a sodium iron phosphate mineral (NaFe2+PO4), that has two metal cations connected to a phosphate tetrahedron. It is structurally similar to the much more common mineral olivine. Maricite is brittle, usually colorless to gray, and has been found in nodules within shale beds often containing other minerals.

Penikisite was discovered by Alan Kulan and Gunar Penikis near Rapid Creek, Yukon Territory. The mineral is a member of the bjarebyite group along with kulanite, ideally BaFe2+2Al2(PO4)3(OH)3, and bjarebyite, ideally BaMn2+2Al2(PO4)3(OH)3. It is among several new minerals that have been discovered in the Rapid Creek and Big Fish areas of Yukon Territory. Kulanite is similar in many ways to penikisite in appearance and properties. The chemical formula for penikisite is Ba(Mg,Fe,Ca)Al2(PO4)2(OH)3. It has a hardness of about 4 and a density of 3.79 g/cm3. Penikisite is unique among the bjarebyite group in being monoclinic and has a biaxial optical class. It comes in shades of blue and green and, when rubbed on a streak plate, is pale green to white in color. Although penikisite and kulanite both range from blue to green, penikisite zones are easily distinguishable from kulanite zones in kulanite-penikisite crystals because they are lighter than the darker kulanite in color. Penikisite is a phosphate and is different from kulanite in that it is a magnesium-rich phosphate whereas kulanite is an iron-rich phosphate.

<span class="mw-page-title-main">Köttigite</span>

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.

Grayite, ThPO4·(H2O), is a thorium phosphate mineral of the Rabdophane group first discovered in 1957 by S.H.U. Bowie in Rhodesia. It is of moderate hardness occurring occasionally in aggregates of hexagonal crystals occasionally but more commonly in microgranular/cryptocrystalline masses. Due to its thorium content, grayite displays some radioactivity although it is only moderate and the mineral displays powder XRD peaks without any metamict-like effects. The color of grayite is most commonly observed as a light to dark reddish brown but has also been observed as lighter yellows with grayish tints. It has a low to moderate hardness with a Mohs hardness of 3–4 and has a specific gravity of 3.7–4.3. It has been found in both intrusive igneous and sedimentary environments.

<span class="mw-page-title-main">Metavivianite</span> Hydrated iron phosphate mineral

Metavivianite is a hydrated iron phosphate mineral found in a number of geological environments. As a secondary mineral it is typically formed from oxidizing dehydrated vivianite. Metavivianite is typically found as dark blue or dark green prismatic to flattened crystals.

References

  1. Warr, L.N. (2021). "IMA–CNMNC approved mineral symbols". Mineralogical Magazine. 85 (3): 291–320. Bibcode:2021MinM...85..291W. doi: 10.1180/mgm.2021.43 . S2CID   235729616.
  2. Santabarbaraite: Santabarbaraite mineral information and data
  3. Santabarbaraite Mineral Data
  4. 1 2 3 4 5 6 7 8 Pratesi G., Cipriani C., Guili G., and Birch W. D. (2003) Santabarbaraite: a new amorphous phosphate mineral. European Journal of Mineralogy.15, 185-192
  5. 1 2 3 Fagel N., Alleman L. Y., Granina L., Hatert F., Thamo-Bozso E., Cloots R. and Andre L. (2005) Vivianite formation and distribution in Lake Baikal sediments. Global and Planetary Change.46, 315-336
  6. Kolitsch U., Bernhardt H. J., Lengauer C. L., Blass G. and Tillmanns E. (2006) Allanpringite, Fe3(PO4)2(OH)3•5H2O, a new ferric iron phosphate from Germany, and its close relation to wavellite. European Journal of Mineralogy.18, 793-801
  7. Athens, Emily (31 May 2021). "How the 'Wandering Meatloaf' Got Its Rock-Hard Teeth". The New York Times . Retrieved 31 May 2021.
  8. Persistent polyamorphism in the chiton tooth: From a new biomineral to inks for additive manufacturing