Tschermakite | |
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General | |
Category | Silicate mineral (amphibole) |
Formula (repeating unit) | ☐Ca2(Mg3Al2)(Si6Al2)O22(OH)2 |
IMA symbol | Tsr [1] |
Strunz classification | 9.DE.10 |
Crystal system | Monoclinic |
Crystal class | Prismatic (2/m) (same H-M symbol) |
Space group | C2/m |
Unit cell | a = 9.762(6) Å b = 17.994(12) Å c = 5.325(6) Å; β = 105.10(8)°; Z = 2 |
Identification | |
Color | Medium to dark green to green-black to black, brown (rare) |
Crystal habit | As prismatic crystals or as reaction rims on other minerals |
Twinning | Simple or multiple twinning parallel to {100} |
Cleavage | Perfect on {110} Parting on {100}{001} |
Fracture | Conchoidal |
Tenacity | Brittle |
Mohs scale hardness | 5–6 |
Luster | Vitreous |
Streak | Pale grey-green |
Diaphaneity | Transparent |
Specific gravity | 3.15 |
Optical properties | Biaxial (−) |
Refractive index | nα = 1.623–1.660 nβ = 1.630–1.680 nγ = 1.638–1.688 |
Birefringence | δ = 0.015–0.028 |
Pleochroism | Visible in browns and greens |
2V angle | Measured: 60° to 90° |
References | [2] [3] [4] [5] |
The endmember hornblende tschermakite (☐Ca2(Mg3Al2)(Si6Al2)O22(OH)2) is a calcium rich monoclinic amphibole mineral. It is frequently synthesized along with its ternary solid solution series members tremolite and cummingtonite so that the thermodynamic properties of its assemblage can be applied to solving other solid solution series from a variety of amphibole minerals.
Tschermakite is an end-member of the hornblende subgroup in the calcic-amphibole group. Calcium-rich amphiboles have the general formula X2–3 Y5 Z8 O22 (OH)2 where X=Ca, Na, K, Mn; Y=Mg, Fe+2, Fe+3, Al, Ti, Mn, Cr, Li, Zn; Z=Si, Al (Deer et al., 1963). The structure of tremolite (Ca2Mg5(Si8O22)(OH,F)2), another calcic amphibole, is commonly used as the standard for calcic amphiboles from which the formulae for their substitutions are derived. The wide range in variety of minerals classified in the amphibole group is due to its great ability for ionic replacement resulting in a widely varying chemical composition. Amphiboles can be classified on the basis of the substitution of ions on the X site as well as the substitution of AlAl for Si(Mg, Fe+2). In the calcium amphiboles like tschermakite Ca2(Mg, Fe2+)3Al2 (Si6 Al2) O22(OH)2, the predominant ion in the X position is occupied by Ca as in tremolite, while the substitution MgSi<->AlAl occurs on the Y and the tetrahedral Z site.
Hornblendes are the most common of the amphiboles and are formed in a wide range of Pressure-Temperature environments. Tschermakite is found in eclogites and ultramafic igneous rocks as well as in medium to high-grade metamorphic rocks. The mineral is widespread throughout the world but has most notably been studied in Greenland, Scotland, Finland, France, and Ukraine (Anthony, 1995). Because amphibole minerals like Tschermakite are hydrous (contain an OH group), they can break down to denser anhydrous minerals like pyroxene or garnet at high temperatures. Conversely, amphiboles can be recomposed from pyroxenes as a result of crystallizing igneous rocks as well as during metamorphism (Léger and Ferry, 1991). Because of this important quality, P-T conditions have repeatedly been calculated for the crystallization of hornblendes in calc-alkaline magmas (Féménias et al., 2006). In addition to studying tschermakitic content in its natural occurrences, geologists have frequently synthesized this mineral in order to further calculate its place as an endmember hornblende.
Tschermakite received its name in honor of the Austrian mineralogist Professor Gustav Tschermak von Seysenegg (1836–1927) whose mineral textbook Lehrbuch der Mineralogie (orig. pub. 1883) was described as the German language equivalent to the works of Edward Salisbury Dana (Mineralogy, 1885).
In 1872 Professor Tschermak founded one of Europe's oldest geoscience journals, Mineralogische Mitteilungen (English: Mineralogical Disclosures, now titled Mineralogy and Petrology). [6] In the first volume of Min. Mitt., Tschermak established some of the early classifications of the amphibole group in relation to the pyroxene group of minerals (Tschermak 1871), which no doubt led to the formula Ca2Mg3Al4Si6O22(OH)2 being known as the Tschermak molecule, this mineral formula was later assigned the name tschermakite as first proposed by Winchell (1945). Professor Tschermak spent many years working as curator for the Imperial Mineralogical Cabinet. The Mineralogical Dept. of the Imperial Natural History Museum in Vienna – an impressive mineral, meteorite and fossil collection has Professor Tschermak to thank for his detailed inventory system that has helped preserve it to this day as well as the expansion of their meteorite collection. He was a full professor of mineralogy and petrography at the University of Vienna as well as a full member of the Imperial Academy of Sciences in Vienna. He was also the first president of the Viennese (now Austrian) Mineralogical Society, founded in 1901. An obituary for "Hofrat Professor Dr. Gustav Tschermak" written by Edward S. Dana (1927) can be found in the 12th volume of American Mineralogist where Dana recalls the two young scientists earlier work together in the Vienna Mineral Cabinet and remarks on Professor Tschermak's vigor and clarity of mind maintained up to his final days. Gustav Tschermak's third child, Erich von Tschermak-Seysenegg (1871–1962) was a renowned botanist who is credited for independently rediscovering Gregor Mendel’s genetic laws of inheritance by working with similar plant breeding experiments.
The amphibole group consists of an orthorhombic and monoclinic series – hornblendes and tschermakite both belong to the latter crystal structure. The crystal group of tschermakite is 2/m.
Tschermakite and all the hornblende varieties are inosilicates, and like the other rock forming amphiboles are double chain silicates (Klein and Hurlbut, 1985). The amphibole structure is characterized by its two double chains of SiO4 tetrahedra (T1 and T2) sandwiching in a strip of cations (M1, M2 and M3 octahedra). Much of the discussions and studies of both tschermakite and tremolite have been to resolve the varying cation placements and Al substitutions that seem to occur on all T and M sites (Najorka and Gottschalk, 2003).
A hand specimen of tschermakite is green to black in color; its streak will be greenish white. It can be transparent to translucent and has a vitreous luster. Tschermakite shows the characteristic amphibole perfect cleavage on [110]. Its average density is 3.24, with a hardness of 5–6; its fracture will be brittle to conchoidal. In thin section its optic sign and 2V angle cover a wide range and are not very useful for identification. It shows a distinct pleochroism in browns and greens.
Much discussion and experimentation on tschermakite has been in relation to it being synthesized along with other calcic-amphiboles to determine the stoichiometric and barometric constraints of the various amphibole solid solutions series. Because of the (Mg, Fe, Ca),Si<->Al, Al tschermak cation exchange that is fundamental to not only the amphibole group but also the pyroxenes, micas and chlorites (Najorka and Gottschalk, 2003; Ishida and Hawthorne, 2006). Tschermakite has been synthesized in numerous experiments along with its ternary solid solution end members tremolite and cummingtonite in order to relate its varying compositions to a specific P and T. The thermodynamic data that results from these tests helps to calculate further geothermobarometric equations in both synthesized and natural forms of a variety of minerals.
In geology and mineralogy, a mineral or mineral species is, broadly speaking, a solid substance with a fairly well-defined chemical composition and a specific crystal structure that occurs naturally in pure form.
Hornblende is a complex inosilicate series of minerals. It is not a recognized mineral in its own right, but the name is used as a general or field term, to refer to a dark amphibole. Hornblende minerals are common in igneous and metamorphic rocks.
Amphibole is a group of inosilicate minerals, forming prism or needlelike crystals, composed of double chain SiO
4 tetrahedra, linked at the vertices and generally containing ions of iron and/or magnesium in their structures. Its IMA symbol is Amp. Amphiboles can be green, black, colorless, white, yellow, blue, or brown. The International Mineralogical Association currently classifies amphiboles as a mineral supergroup, within which are two groups and several subgroups.
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.
Actinolite is an amphibole silicate mineral with the chemical formula Ca2(Mg4.5–2.5Fe2+0.5–2.5)Si8O22(OH)2.
Amphibolite is a metamorphic rock that contains amphibole, especially hornblende and actinolite, as well as plagioclase feldspar, but with little or no quartz. It is typically dark-colored and dense, with a weakly foliated or schistose (flaky) structure. The small flakes of black and white in the rock often give it a salt-and-pepper appearance.
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.
Cummingtonite is a metamorphic amphibole with the chemical composition (Mg,Fe2+
)
2(Mg,Fe2+
)
5Si
8O
22(OH)
2, magnesium iron silicate hydroxide.
Anthophyllite is an orthorhombic amphibole mineral: ☐Mg2Mg5Si8O22(OH)2 (☐ is for a vacancy, a point defect in the crystal structure), magnesium iron inosilicate hydroxide. Anthophyllite is polymorphic with cummingtonite. Some forms of anthophyllite are lamellar or fibrous and are classed as asbestos. The name is derived from the Latin word anthophyllum, meaning clove, an allusion to the most common color of the mineral. The Anthophyllite crystal is characterized by its perfect cleavage along directions 126 degrees and 54 degrees.
Gustav Tschermak von Seysenegg was an Austrian mineralogist.
Geothermobarometry is the methodology for estimating the pressure and temperature history of rocks. Geothermobarometry is a combination of geobarometry, where the pressure attained by a mineral assemblage is estimated, and geothermometry where the temperature attained by a mineral assemblage is estimated.
A metamorphic facies is a set of mineral assemblages in metamorphic rocks formed under similar pressures and temperatures. The assemblage is typical of what is formed in conditions corresponding to an area on the two dimensional graph of temperature vs. pressure. Rocks which contain certain minerals can therefore be linked to certain tectonic settings, times and places in the geological history of the area. The boundaries between facies are wide because they are gradational and approximate. The area on the graph corresponding to rock formation at the lowest values of temperature and pressure is the range of formation of sedimentary rocks, as opposed to metamorphic rocks, in a process called diagenesis.
Gedrite is a crystal belonging to the orthorhombic ferromagnesian subgroup of the amphibole supergroup of the double chain inosilicate minerals with the ideal chemical formula Mg2(Mg3Al2)(Si6Al2)O22(OH)2.
Edenite or edenitic hornblende is a double chain silicate mineral of the amphibole group with the general chemical composition NaCa2Mg5(Si7Al)O22(OH)2. Edenite is named for the locality of Edenville, Orange County, New York, where it was first described.
This list gives an overview of the classification of minerals (silicates) and includes mostly International Mineralogical Association (IMA) recognized minerals and its groupings. This list complements the List of minerals recognized by the International Mineralogical Association series of articles and List of minerals. Rocks, ores, mineral mixtures, non-IMA approved minerals and non-named minerals are mostly excluded.
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.
Jimthompsonite is a magnesium iron silicate mineral with chemical formula (Mg,Fe2+)5Si6O16(OH)2. It is a triple chain silicate (or inosilicate) along with clinojimthompsonite and chesterite. They were described in 1977 by Burham and Veblen. They attracted great mineralogical attention because they were the first examples of new chain silicate structures among a large group known as biopyriboles whose name is derived from the words biotite, pyroxene, and amphiboles.
Ferrogedrite is an amphibole mineral with the complex chemical formula of ☐Fe2+2(Fe2+3Al2)(Si6Al2)O22(OH)2. It is sodium and calcium poor, making it part of the magnesium-iron-manganese-lithium amphibole subgroup. Defined as less than 1.00 apfu (atoms per formula unit) of Na + Ca and consisting of greater than 1.00 apfu of (Mg, Fe2+, Mn2+, Li) separating it from the calcic-sodic amphiboles. It is related to anthophyllite amphibole and gedrite through coupled substitution of (Al, Fe3+) for (Mg, Fe2+, Mn) and Al for Si. and determined by the content of silicon in the standard cell.
Timothy John Barrington Holland is a petrologist and Emeritus Professor in the Department of Earth Sciences at the University of Cambridge.
Coupled substitution is the geological process by which two elements simultaneous substitute into a crystal in order to maintain overall electrical neutrality and keep the charge constant. In forming a solid solution series, ionic size is more important than ionic charge, as this can be compensated for elsewhere in the structure.