Magnesiohastingsite

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Magnesiohastingsite
Magnesiohastingsite.jpg
Magnesiohastingsite from Bratislava, Slovakia. Specimen size 4.5 cm
General
Category Amphibole
Formula
(repeating unit)
NaCa2(Mg4Fe3+)(Si6Al2)O22(OH)2 [1]
Strunz classification 9.DE.15 (10 ed)
8/F.10-130 (8 ed)
Dana classification 66.01.03a.14
Crystal system Monoclinic
Crystal class Prismatic (2/m)
(same H-M symbol)
Space group C2/m
Identification
Formula mass 864.69 g/mol [2]
ColorGreen to dark green or black
Twinning Simple or multiple twinning parallel to {100} [3]
Cleavage Good on {110} with intersections at about 56° and 124°. Partings on {001}, {100} [3]
Tenacity Brittle
Mohs scale hardness5 to 6
Luster Vitreous
Streak Pale grey-green to pale brownish-green [4]
Diaphaneity Subopaque
Specific gravity 3.16 to 3.22
Optical propertiesBiaxial (-)
Solubility Insoluble in HCl [5]
Other characteristicsNot radioactive
References [6] [2] [3] [4] [7] [1] [5] [8]

Magnesiohastingsite is a calcium-containing amphibole and a member of the hornblende group. [5] It is an inosilicate (chain silicate) with the formula NaCa2(Mg4Fe3+)(Si6Al2)O22(OH)2 [1] and molar mass 864.69 g. [2] 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. [9] 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. [4]

Contents

Calcic (containing calcium) amphiboles include: [5]

The hornblende group includes: [5]

Unit cell

Magnesiohastingsite belongs to the monoclinic crystal system, point group 2/m, space group C2/m. It has two formula units per unit cell (Z = 2). The unit cell parameters both for natural and for synthetic [9] material are a = 9.9 Å, b = 18.0 Å, c = 5.3 Å, β = 105°. [3] [4]

Structure

Double Chain of SiO4 Tetrahedra Tremolith-Si-double-chain.gif
Double Chain of SiO4 Tetrahedra

The structure of all amphiboles is based on a double chain of linked SiO4 tetrahedra, with composition (Si4O11)n. The inner tetrahedra are referred to as T1 and the outer ones as T2. The pattern in the double chain repeats after a block of two T1 and two T2 tetrahedra, with a repeat distance of approximately 5.3 Å, and this determines the length of the unit cell along the c crystal axis. The tetrahedra within a chain all point outwards in the same direction, and the chains are linked back-to-back by cations to form I-beams. The I-beams themselves are then linked together to form the complete structure.

Optical properties

The mineral is subopaque and vitreous, green to dark green or black in color and with a pale grey-green to pale brownish-green streak. [4] It is biaxial (-) with refractive indices for natural material in the range nα = 1.652 to 1.676, nβ = 1.661 to 1.695, nγ = 1.666 to 1.706. Synthetic material has nα = 1.642 to 1.657, nγ = 1.653 to 1.672. [9] An increase in magnesium content causes a decrease in refractive indices. [10] The maximum birefringence (the difference in refractive index between light travelling through the crystal with different polarizations) is δ = 0.012 to 0.033. The optic angle 2V is the angle between the two optic axes in a biaxial crystal. Measured values of 2V for this mineral vary widely from about 60° to 90°. It is also possible to calculate a theoretical value of 2V from the measured values of the refractive indices. The calculated value varies from 68° to 88°. [2] [4] The direction perpendicular to the plane containing the two optic axes is called the optical direction Y. In magnesiohastingsite Y is parallel to the b crystal axis. [3] [10] The optical direction Z lies in the plane containing the two optic axes and bisects the angle between them. In magnesiohastingsite the angle between Z and the c crystal axis is 15° to 19°. [3] If the color of the incident light is changed, then the refractive indices are modified, and the value of 2V changes. This is known as dispersion of the optic axes. For magnesiohastingsite the effect is weak, with 2V larger for red light than for violet light (r>v). [2] [4] [10]

Pleochroism is variable in green, yellow-green, bluish-green and brown. [5]

Physical properties

Cleavage is good with cleavage surfaces intersecting at about 56° and 124°, as is common with all the amphiboles. The mineral displays simple or multiple twinning parallel to a prism face. [3] It is a brittle mineral, with Mohs hardness 5 to 6 and specific gravity 3.2, with increasing magnesium content causing a decrease in specific gravity. [10] It is not radioactive [2] and it is insoluble in hydrochloric acid. [5]

Occurrence and associations

The type locality is in the Canadian National Railway tunnel, Montreal, Quebec, Canada. [4] It is common in amphibolite, schist and pegmatitic gabbro. It is also found in welded tuffs, granodiorite, granite and tonalite. [3] Associated minerals include quartz, orthoclase, plagioclase, biotite, magnetite and apatite. [3] Barkevikite and the magnesium-rich members of the hastingsite group are found in diorite, essexite and related calcium-rich rocks. [10] Localities include:

Related Research Articles

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<span class="mw-page-title-main">Amphibole</span> Group of inosilicate minerals

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4
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<span class="mw-page-title-main">Vivianite</span> Fe(II) phosphate mineral

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3
(PO
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)
2
·8H
2
O
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<span class="mw-page-title-main">Scolecite</span>

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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.

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

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<span class="mw-page-title-main">Nyerereite</span> Very rare sodium calcium carbonate mineral

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<span class="mw-page-title-main">Tschermakite</span> Amphibole, double chain inosilicate mineral

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<span class="mw-page-title-main">Plancheite</span> Hydrated copper silicate mineral

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

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<span class="mw-page-title-main">Köttigite</span> Rare hydrated zinc arsenate

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.

<span class="mw-page-title-main">Carminite</span> Anhydrous arsenate mineral containing hydroxyl

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.

<span class="mw-page-title-main">Serpierite</span> Rare sky-blue coloured hydrated sulfate mineral

Serpierite (Ca(Cu,Zn)4(SO4)2(OH)6·3H2O) is a rare, sky-blue coloured hydrated sulfate mineral, often found as a post-mining product. It is a member of the devilline group, which has members aldridgeite (Cd,Ca)(Cu,Zn)4(SO4)2(OH)6·3H2O, campigliaite Cu4Mn2+(SO4)2(OH)6·4H2O, devilline CaCu4(SO4)2(OH)6·3H2O, kobyashevite Cu5(SO4)2(OH)6·4H2O, lautenthalite PbCu4(SO4)2(OH)6·3H2O and an unnamed dimorph of devilline. It is the calcium analogue of aldridgeite and it is dimorphous with orthoserpierite CaCu4(SO4)2(OH)6·3H2O.

<span class="mw-page-title-main">Mottramite</span> Orthorhombic anhydrous vanadate hydroxide mineral

Mottramite is an orthorhombic anhydrous vanadate hydroxide mineral, PbCu(VO4)(OH), at the copper end of the descloizite subgroup. It was formerly called cuprodescloizite or psittacinite (this mineral characterized in 1868 by Frederick Augustus Genth). Duhamelite is a calcium- and bismuth-bearing variety of mottramite, typically with acicular habit.

<span class="mw-page-title-main">Talmessite</span> Hydrated calcium magnesium arsenate

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.

References

  1. 1 2 3 RRUFF.info/ima
  2. 1 2 3 4 5 6 Webmineral data
  3. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 Handbook of Mineralogy
  4. 1 2 3 4 5 6 7 8 Mindat.org
  5. 1 2 3 4 5 6 7 Deer, Howie and Zussman (1997) Rock-forming minerals V2B:234-601
  6. Mineralienatlas
  7. 1 2 3 Gaines et al (1997) Dana’s New Mineralogy Eighth Edition. Wiley
  8. IMA Master List
  9. 1 2 3 Semet, M P (1973) American Mineralogist 58:480-494
  10. 1 2 3 4 5 Billings, M P (1928) American Mineralogist 13:287

Jmol: http://rruff.geo.arizona.edu/AMS/viewJmol.php?id=11242