Bustamite

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Bustamite
Bustamite.jpg
Bustamite (pink) with galena (grey) from Broken Hill, New South Wales, Australia. Specimen size 3.7 cm.
General
Category Inosilicate
Formula
(repeating unit)
CaMn2+Si2O6 [1]
IMA symbol Bst [2]
Strunz classification 9.DG.05 (10 ed)
8/F.18.40 (8 ed)
Dana classification 65.2.1.2
Crystal system Triclinic
Crystal class Pinacoidal 1
(same H-M symbol)
Space group I1
Identification
ColorLight pink to brownish red Pink color fades on exposure to sunlight
Crystal habit Usually tabular or equant to prismatic; commonly massive, often compact and fibrous
Twinning Rare. Simple twins with (110) as the composition plane
Cleavage {100} perfect; {110} and {110} good; {010} poor
Mohs scale hardness5.5 to 6.5
Luster Vitreous
Streak White
Diaphaneity Translucent to transparent
Specific gravity 3.32 to 3.43 (observed) 3.40 (calculated)
Optical propertiesBiaxial (−), 2V=34° to 60°
Refractive index nα = 1.640 – 1.695, nβ = 1.651 – 1.708, nγ = 1.653 – 1.710 [3]
Birefringence δ = 0.013 – 0.015
Dispersion r < v weak to strong
Pleochroism Weak, X and Z orange, Y rose
Solubility Partly soluble in HCl. [3]
Other characteristicslattice: A B1
Specimens from the Franklin Mine are fluorescent red in longwave ultraviolet light. [4] Not radioactive
References [5] [6] [7] [8]

Bustamite is a calcium manganese inosilicate (chain silicate) and a member of the wollastonite group. Magnesium, zinc and iron are common impurities substituting for manganese. Bustamite is the high-temperature polymorph of CaMnSi2O6 and johannsenite is the low temperature polymorph. The inversion takes place at 830 °C (1,530 °F), but may be very slow. [3]
Bustamite could be confused with light-colored rhodonite or pyroxmangite, but both these minerals are biaxial (+) whereas bustamite is biaxial (−).

Contents

Cell parameters

There is considerable variety in the literature about the size and type of the unit cell, the formula to be used, and the value of Z, the number of formula units per unit cell.

Bustamite is a triclinic mineral, which could be described by a primitive unit cell, but the larger A-centered cell is often preferred, in order to facilitate comparison with the similar mineral wollastonite. [9]

The formula for bustamite is CaMn(SiO3)2 [1] but it is sometimes written (Ca,Mn)SiO3, and changing the formula in this way will change the value of Z. The structure is chains of SiO4 tetrahedra with repeat unit of three tetrahedra, unlike the pyroxenes where the repeat unit is two. [10] Ca++ and Mn++ are positioned between the chains. There are 12 tetrahedra in the A-centered unit cell. [9]

The unit cell, the formula and Z cannot be taken separately; they are interlinked and form a consistent set of values. This article adopts the A-centred unit cell (space group A1) with a = 7.736  Å, b = 7.157 Å and c = 13.824 Å, the formula CaMn(SO3)3 and Z = 6. Deer et al. [3] take the formula as (Mn,Ca,Fe)[SiO3] so their value of Z is doubled to 12. Mindat [7] apparently gives the lattice parameters for a face-centred cell, [9] although they give the space group as P1.

Type locality

The type locality was originally taken as Tetela de Jonotla, Puebla, Mexico, and the mineral was named for the Mexican mineralogist and botanist Miguel Bustamante y Septiem (1790–1844). [11] The material from Puebla, however, was later found to be a mixture of johannsenite and rhodonite, [10] so the type locality is now the Franklin Mine, Franklin, Sussex County, New Jersey, US. [7]

Both bustamite and johansennite are found at Franklin. [4] Bustamite is moderately common there and occurs in a variety of assemblages, associated with rhodonite and tephroite, calcite and tephroite or glaucochroite and tephroite. Vesuvianite, wollastonite, garnet, diopside, willemite, johannsenite, margarosanite and clinohedrite also may be present.

Environment

Bustamite typically results from metamorphism of manganese-bearing sediments, with attendant metasomatism. At the (new) type locality, Franklin, the oldest rocks are Precambrian gneisses of mixed sedimentary and volcanic origin. Franklin Marble was deposited within these rocks, along with sediments containing zinc, manganese and iron minerals. These sediments were metamorphosed later in the Precambrian, then the rocks were uplifted from the late Precambrian into the Cambrian and quartzite was deposited on the eroded surface. In Cambrian-Ordovician time the quartzite was in turn overlain by limestone, and the rocks have been subject to uplift and erosion up to the present time. [12]

Related Research Articles

<span class="mw-page-title-main">Pyroxene</span> Group of inosilicate minerals with single chains of silica tetrahedra

The pyroxenes are a group of important rock-forming inosilicate minerals found in many igneous and metamorphic rocks. Pyroxenes have the general formula XY(Si,Al)2O6, where X represents calcium (Ca), sodium (Na), iron or magnesium (Mg) and more rarely zinc, manganese or lithium, and Y represents ions of smaller size, such as chromium (Cr), aluminium (Al), magnesium (Mg), cobalt (Co), manganese (Mn), scandium (Sc), titanium (Ti), vanadium (V) or even iron. Although aluminium substitutes extensively for silicon in silicates such as feldspars and amphiboles, the substitution occurs only to a limited extent in most pyroxenes. They share a common structure consisting of single chains of silica tetrahedra. Pyroxenes that crystallize in the monoclinic system are known as clinopyroxenes and those that crystallize in the orthorhombic system are known as orthopyroxenes.

<span class="mw-page-title-main">Wollastonite</span> Single chain calcium inosilicate (CaSiO3)

Wollastonite is a calcium inosilicate mineral (CaSiO3) that may contain small amounts of iron, magnesium, and manganese substituting for calcium. It is usually white. It forms when impure limestone or dolomite is subjected to high temperature and pressure, which sometimes occurs in the presence of silica-bearing fluids as in skarns or in contact with metamorphic rocks. Associated minerals include garnets, vesuvianite, diopside, tremolite, epidote, plagioclase feldspar, pyroxene and calcite. It is named after the English chemist and mineralogist William Hyde Wollaston (1766–1828).

<span class="mw-page-title-main">Enstatite</span> Pyroxene: magnesium-iron silicate with MgSiO3 and FeSiO3 end-members

Enstatite is a mineral; the magnesium endmember of the pyroxene silicate mineral series enstatite (MgSiO3) – ferrosilite (FeSiO3). The magnesium rich members of the solid solution series are common rock-forming minerals found in igneous and metamorphic rocks. The intermediate composition, (Mg,Fe)SiO
3
, has historically been known as hypersthene, although this name has been formally abandoned and replaced by orthopyroxene. When determined petrographically or chemically the composition is given as relative proportions of enstatite (En) and ferrosilite (Fs) (e.g., En80Fs20).

<span class="mw-page-title-main">Silicate mineral</span> Rock-forming minerals with predominantly silicate anions

Silicate minerals are rock-forming minerals made up of silicate groups. They are the largest and most important class of minerals and make up approximately 90 percent of Earth's crust.

<span class="mw-page-title-main">Rhodonite</span> Single chain manganese inosilicate (MnSiO3)

Rhodonite is a manganese inosilicate, with the formula (Mn, Fe, Mg, Ca)SiO3, and member of the pyroxenoid group of minerals, crystallizing in the triclinic system. It commonly occurs as cleavable to compact masses with a rose-red color (its name comes from Ancient Greek ῥόδον (rhódon) 'rose'), often tending to brown due to surface oxidation. The rose-red hue is caused by the manganese cation (Mn2+).

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

Tephroite is the manganese endmember of the olivine group of nesosilicate minerals with the formula Mn2SiO4. A solid solution series exists between tephroite and its analogues, the group endmembers fayalite and forsterite. Divalent iron or magnesium may readily replace manganese in the olivine crystal structure.

<span class="mw-page-title-main">Todorokite</span> Hydrous manganese oxide mineral

Todorokite is a complex hydrous manganese oxide mineral with generic chemical formula (Na,Ca,K,Ba,Sr)
1-x
(Mn,Mg,Al)
6
O
12
·3-4H
2
O
. 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.

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

Galaxite, also known as 'mangan-spinel' is an isometric mineral belonging to the spinel group of oxides with the ideal chemical formula Mn2+Al2O4.

<span class="mw-page-title-main">Kutnohorite</span> Mineral of calcium manganese carbonate

Kutnohorite is a rare calcium manganese carbonate mineral with magnesium and iron that is a member of the dolomite group. It forms a series with dolomite, and with ankerite. The end member formula is CaMn2+(CO3)2, but Mg2+ and Fe2+ commonly substitute for Mn2+, with the manganese content varying from 38% to 84%, so the formula Ca(Mn2+,Mg,Fe2+)(CO3)2 better represents the species. It was named by Professor Bukowsky in 1901 after the type locality of Kutná Hora, Bohemia, in the Czech Republic. It was originally spelt "kutnahorite" but "kutnohorite" is the current IMA-approved spelling.

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.

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

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. 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.

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

Pyroxmangite has the general chemical formula of MnSiO3. It is the high-pressure, low-temperature dimorph of rhodonite.

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

Kanoite is a light pinkish brown silicate mineral that is found in metamorphic rocks. It is an inosilicate and has a chemical formula of (Mg,Mn2+)2Si2O6. It is a member of pyroxene group and clinopyroxene subgroup.

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

Whiteite is a rare hydrated hydroxyphosphate mineral.

<span class="mw-page-title-main">Pimelite</span> Nickel-rich smectite deprecated as mineral species in 2006

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.

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

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.

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

Serandite is a mineral with formula Na(Mn2+,Ca)2Si3O8(OH). The mineral was discovered in Guinea in 1931 and named for J. M. Sérand. Serandite is generally red, brown, black or colorless. The correct name lacks an accent.

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

Fianelite is a mineral belonging to the manganese vanadate category, found in iron-manganese ores. Named after the place where it was found, Fianel, a mine located in Val Ferrera, in the canton of Graubünden, Swiss. This mineral is found in small amounts in metamorphosed iron-manganese ores. This is the last crystallization of vanadate at the site since medaite was the last vanadate mineral being crystallized, but because of retrograde metamorphism, occurring at the place, vanadium moved into medaite veinlets, forming cross-cutting fianelite on medaite.

References

  1. 1 2 "IMA Mineral List with Database of Mineral Properties".
  2. 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.
  3. 1 2 3 4 Deer, W A, Howie, R A and Zussman, J (1978) Rock-Forming Minerals, 2nd edition, Volume 2A, pages 574-585
  4. 1 2 "Bustamite". Archived from the original on 2014-07-01.
  5. Mineralienatlas
  6. "Bustamite Mineral Data".
  7. 1 2 3 "Bustamite - Mineral information". www.mindat.org.
  8. "Bustamite" (PDF). rruff.geo.arizona.edu.
  9. 1 2 3 Peacor and Prewitt (1963) The American Mineralogist volume 48 pages 588 to 596
  10. 1 2 Dana's New Mineralogy Eighth Edition, Wiley
  11. Alexandre Brongniart, « Sur la Bustamite, Bisilicate de manganèse et de chaux du Mexique », Annales des sciences naturelles, vol. VIII, Crochard, Libraire-Éditeur, Paris, 1826, p. 411-418
  12. Drake, A A (1990) The regional geologic setting of the Franklin-Sterling Hill district. Symposium on the character and origin of the Franklin-Sterling Hill orebodies, Proceedings, pp. 14-31, Lehigh University, Bethlehem, Pennsylvania