Portal:Minerals
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The Minerals Portal
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.
The geological definition of mineral normally excludes compounds that occur only in living organisms. However, some minerals are often biogenic (such as calcite) or organic compounds in the sense of chemistry (such as mellite). Moreover, living organisms often synthesize inorganic minerals (such as hydroxylapatite) that also occur in rocks.
The concept of mineral is distinct from rock, which is any bulk solid geologic material that is relatively homogeneous at a large enough scale. A rock may consist of one type of mineral or may be an aggregate of two or more different types of minerals, spacially segregated into distinct phases.
Some natural solid substances without a definite crystalline structure, such as opal or obsidian, are more properly called mineraloids. If a chemical compound occurs naturally with different crystal structures, each structure is considered a different mineral species. Thus, for example, quartz and stishovite are two different minerals consisting of the same compound, silicon dioxide. (Full article...)
Mineralogy is a subject of geology specializing in the scientific study of the chemistry, crystal structure, and physical (including optical) properties of minerals and mineralized artifacts. Specific studies within mineralogy include the processes of mineral origin and formation, classification of minerals, their geographical distribution, as well as their utilization. (Full article...)
Selected articles
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The mineral pyrite (/ˈpaɪraɪt/ PY-ryte), or iron pyrite, also known as fool's gold, is an iron sulfide with the chemical formula FeS2 (iron (II) disulfide). Pyrite is the most abundant sulfide mineral.
Pyrite's metallic luster and pale brass-yellow hue give it a superficial resemblance to gold, hence the well-known nickname of fool's gold. The color has also led to the nicknames brass, brazzle, and brazil, primarily used to refer to pyrite found in coal.
The name pyrite is derived from the Greek πυρίτης λίθος (pyritēs lithos), 'stone or mineral which strikes fire', in turn from πῦρ (pŷr), 'fire'. In ancient Roman times, this name was applied to several types of stone that would create sparks when struck against steel; Pliny the Elder described one of them as being brassy, almost certainly a reference to what is now called pyrite.
By Georgius Agricola's time, c. 1550, the term had become a generic term for all of the sulfide minerals. (Full article...) -
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In crystallography, the cubic (or isometric) crystal system is a crystal system where the unit cell is in the shape of a cube. This is one of the most common and simplest shapes found in crystals and minerals.
There are three main varieties of these crystals:- Primitive cubic (abbreviated cP and alternatively called simple cubic)
- Body-centered cubic (abbreviated cI or bcc)
- Face-centered cubic (abbreviated cF or fcc)
Note: the term fcc is often used in synonym for the cubic close-packed or ccp structure occurring in metals. However, fcc stands for a face-centered-cubic Bravais lattice, which is not necessarily close-packed when a motif is set onto the lattice points. E.g. the diamond and the zincblende lattices are fcc but not close-packed.
Each is subdivided into other variants listed below. Although the unit cells in these crystals are conventionally taken to be cubes, the primitive unit cells often are not. (Full article...) -
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Chalcopyrite (/ˌkælkəˈpaɪˌraɪt, -koʊ-/ KAL-kə-PY-ryte, -koh-) is a copper iron sulfide mineral and the most abundant copper ore mineral. It has the chemical formula CuFeS2 and crystallizes in the tetragonal system. It has a brassy to golden yellow color and a hardness of 3.5 to 4 on the Mohs scale. Its streak is diagnostic as green-tinged black.
On exposure to air, chalcopyrite tarnishes to a variety of oxides, hydroxides, and sulfates. Associated copper minerals include the sulfides bornite (Cu5FeS4), chalcocite (Cu2S), covellite (CuS), digenite (Cu9S5); carbonates such as malachite and azurite, and rarely oxides such as cuprite (Cu2O). It is rarely found in association with native copper. Chalcopyrite is a conductor of electricity.
Copper can be extracted from chalcopyrite ore using various methods. The two predominant methods are pyrometallurgy and hydrometallurgy, the former being the most commercially viable. (Full article...) -
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Corundum is a crystalline form of aluminium oxide (Al2O3) typically containing traces of iron, titanium, vanadium, and chromium. It is a rock-forming mineral. It is a naturally transparent material, but can have different colors depending on the presence of transition metal impurities in its crystalline structure. Corundum has two primary gem varieties: ruby and sapphire. Rubies are red due to the presence of chromium, and sapphires exhibit a range of colors depending on what transition metal is present. A rare type of sapphire, padparadscha sapphire, is pink-orange.
The name "corundum" is derived from the Tamil-Dravidian word kurundam (ruby-sapphire) (appearing in Sanskrit as kuruvinda).
Because of corundum's hardness (pure corundum is defined to have 9.0 on the Mohs scale), it can scratch almost all other minerals. It is commonly used as an abrasive on sandpaper and on large tools used in machining metals, plastics, and wood. Emery, a variety of corundum with no value as a gemstone, is commonly used as an abrasive. It is a black granular form of corundum, in which the mineral is intimately mixed with magnetite, hematite, or hercynite.
In addition to its hardness, corundum has a density of 4.02 g/cm3 (251 lb/cu ft), which is unusually high for a transparent mineral composed of the low-atomic mass elements aluminium and oxygen. (Full article...) -
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Beryl (/ˈbɛrəl/ BERR-əl) is a mineral composed of beryllium aluminium silicate with the chemical formula Be3Al2Si6O18. Well-known varieties of beryl include emerald and aquamarine. Naturally occurring hexagonal crystals of beryl can be up to several meters in size, but terminated crystals are relatively rare. Pure beryl is colorless, but it is frequently tinted by impurities; possible colors are green, blue, yellow, pink, and red (the rarest). It is an ore source of beryllium. (Full article...) -
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Malachite is a copper carbonate hydroxide mineral, with the formula Cu2CO3(OH)2. This opaque, green-banded mineral crystallizes in the monoclinic crystal system, and most often forms botryoidal, fibrous, or stalagmitic masses, in fractures and deep, underground spaces, where the water table and hydrothermal fluids provide the means for chemical precipitation. Individual crystals are rare, but occur as slender to acicular prisms. Pseudomorphs after more tabular or blocky azurite crystals also occur. (Full article...) -
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Tourmaline (/ˈtʊərməlɪn, -ˌliːn/ TOOR-mə-lin, -leen) is a crystalline silicate mineral group in which boron is compounded with elements such as aluminium, iron, magnesium, sodium, lithium, or potassium. This gemstone comes in a wide variety of colors.
The name is derived from the Sinhalese tōramalli (ටෝරමල්ලි), which refers to the carnelian gemstones. (Full article...) -
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Apatite is a group of phosphate minerals, usually hydroxyapatite, fluorapatite and chlorapatite, with high concentrations of OH−, F− and Cl− ion, respectively, in the crystal. The formula of the admixture of the three most common endmembers is written as Ca10(PO4)6(OH,F,Cl)2, and the crystal unit cell formulae of the individual minerals are written as Ca10(PO4)6(OH)2, Ca10(PO4)6F2 and Ca10(PO4)6Cl2.
The mineral was named apatite by the German geologist Abraham Gottlob Werner in 1786, although the specific mineral he had described was reclassified as fluorapatite in 1860 by the German mineralogist Karl Friedrich August Rammelsberg. Apatite is often mistaken for other minerals. This tendency is reflected in the mineral's name, which is derived from the Greek word ἀπατάω (apatáō), which means to deceive. (Full article...) -
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Halite (/ˈhælaɪt, ˈheɪlaɪt/ HAL-yte, HAY-lyte), commonly known as rock salt, is a type of salt, the mineral (natural) form of sodium chloride (NaCl). Halite forms isometric crystals. The mineral is typically colorless or white, but may also be light blue, dark blue, purple, pink, red, orange, yellow or gray depending on inclusion of other materials, impurities, and structural or isotopic abnormalities in the crystals. It commonly occurs with other evaporite deposit minerals such as several of the sulfates, halides, and borates. The name halite is derived from the Ancient Greek word for "salt", ἅλς (háls). (Full article...) -
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Rutile is an oxide mineral composed of titanium dioxide (TiO2), the most common natural form of TiO2. Rarer polymorphs of TiO2 are known, including anatase, akaogiite, and brookite.
Rutile has one of the highest refractive indices at visible wavelengths of any known crystal and also exhibits a particularly large birefringence and high dispersion. Owing to these properties, it is useful for the manufacture of certain optical elements, especially polarization optics, for longer visible and infrared wavelengths up to about 4.5 micrometres. Natural rutile may contain up to 10% iron and significant amounts of niobium and tantalum.
Rutile derives its name from the Latin rutilus ('red'), in reference to the deep red color observed in some specimens when viewed by transmitted light. Rutile was first described in 1803 by Abraham Gottlob Werner using specimens obtained in Horcajuelo de la Sierra, Madrid (Spain), which is consequently the type locality. (Full article...) -
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Mineralogy is a subject of geology specializing in the scientific study of the chemistry, crystal structure, and physical (including optical) properties of minerals and mineralized artifacts. Specific studies within mineralogy include the processes of mineral origin and formation, classification of minerals, their geographical distribution, as well as their utilization. (Full article...) -
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Fluorite (also called fluorspar) is the mineral form of calcium fluoride, CaF2. It belongs to the halide minerals. It crystallizes in isometric cubic habit, although octahedral and more complex isometric forms are not uncommon.
The Mohs scale of mineral hardness, based on scratch hardness comparison, defines value 4 as fluorite.
Pure fluorite is colourless and transparent, both in visible and ultraviolet light, but impurities usually make it a colorful mineral and the stone has ornamental and lapidary uses. Industrially, fluorite is used as a flux for smelting, and in the production of certain glasses and enamels. The purest grades of fluorite are a source of fluoride for hydrofluoric acid manufacture, which is the intermediate source of most fluorine-containing fine chemicals. Optically clear transparent fluorite has anomalous partial dispersion, that is, its refractive index varies with the wavelength of light in a manner that differs from that of commonly used glases, so fluorite is useful in making apochromatic lenses, making it valuable, particularly in photographic optics. Fluorite optics are also usable in the far-ultraviolet and mid-infrared ranges, where conventional glasses are too opaque for use. Fluorite also has low dispersion, and a high refractive index for its density, which can make it useful for some specialized purposes in optics. (Full article...) -
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In crystallography, a crystal system is a set of point groups (a group of geometric symmetries with at least one fixed point). A lattice system is a set of Bravais lattices. Space groups are classified into crystal systems according to their point groups, and into lattice systems according to their Bravais lattices. Crystal systems that have space groups assigned to a common lattice system are combined into a crystal family.
The seven crystal systems are triclinic, monoclinic, orthorhombic, tetragonal, trigonal, hexagonal, and cubic. Informally, two crystals are in the same crystal system if they have similar symmetries (though there are many exceptions). (Full article...) -
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Micas (/ˈmaɪkəz/ MY-kəz) are a group of silicate minerals whose outstanding physical characteristic is that individual mica crystals can easily be split into extremely thin elastic plates. This characteristic is described as perfect basal cleavage. Mica is common in igneous and metamorphic rock and is occasionally found as small flakes in sedimentary rock. It is particularly prominent in many granites, pegmatites, and schists, and "books" (large individual crystals) of mica several feet across have been found in some pegmatites.
Micas are used in products such as drywalls, paints, fillers, especially in parts for automobiles, roofing and shingles, as well as in electronics. The mineral is used in cosmetics and food to add "shimmer" or "frost." (Full article...) -
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Opal is a hydrated amorphous form of silica (SiO2·nH2O); its water content may range from 3% to 21% by weight, but is usually between 6% and 10%. Due to its amorphous property, it is classified as a mineraloid, unlike crystalline forms of silica, which are considered minerals. It is deposited at a relatively low temperature and may occur in the fissures of almost any kind of rock, being most commonly found with limonite, sandstone, rhyolite, marl, and basalt.
The name opal is believed to be derived from the Sanskrit word upala (उपल), which means 'jewel', and later the Greek derivative opállios (ὀπάλλιος).
There are two broad classes of opal: precious and common. Precious opal displays play-of-color (iridescence); common opal does not. Play-of-color is defined as "a pseudo chromatic optical effect resulting in flashes of colored light from certain minerals, as they are turned in white light." The internal structure of precious opal causes it to diffract light, resulting in play-of-color. Depending on the conditions in which it formed, opal may be transparent, translucent, or opaque, and the background color may be white, black, or nearly any color of the visual spectrum. Black opal is considered the rarest, while white, gray, and green opals are the most common. (Full article...) -
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Kaolinite (/ˈkeɪ.ələˌnaɪt, -lɪ-/ KAY-ə-lə-nyte, -lih-; also called kaolin) is a clay mineral, with the chemical composition: Al2Si2O5(OH)4. It is a layered silicate mineral, with one tetrahedral sheet of silica (SiO4) linked through oxygen atoms to one octahedral sheet of alumina (AlO6).
Kaolinite is a soft, earthy, usually white, mineral (dioctahedral phyllosilicate clay), produced by the chemical weathering of aluminium silicate minerals like feldspar. It has a low shrink–swell capacity and a low cation-exchange capacity (1–15 meq/100 g).
Rocks that are rich in kaolinite, and halloysite, are known as kaolin (/ˈkeɪ.əlɪn/) or china clay. In many parts of the world kaolin is colored pink-orange-red by iron oxide, giving it a distinct rust hue. Lower concentrations of iron oxide yield the white, yellow, or light orange colors of kaolin. Alternating lighter and darker layers are sometimes found, as at Providence Canyon State Park in Georgia, United States.
Kaolin is an important raw material in many industries and applications. Commercial grades of kaolin are supplied and transported as powder, lumps, semi-dried noodle or slurry. Global production of kaolin in 2021 was estimated to be 45 million tonnes, with a total market value of $US4.24 billion. (Full article...) -
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Magnetite is a mineral and one of the main iron ores, with the chemical formula Fe2+Fe3+2O4. It is one of the oxides of iron, and is ferrimagnetic; it is attracted to a magnet and can be magnetized to become a permanent magnet itself. With the exception of extremely rare native iron deposits, it is the most magnetic of all the naturally occurring minerals on Earth. Naturally magnetized pieces of magnetite, called lodestone, will attract small pieces of iron, which is how ancient peoples first discovered the property of magnetism.
Magnetite is black or brownish-black with a metallic luster, has a Mohs hardness of 5–6 and leaves a black streak. Small grains of magnetite are very common in igneous and metamorphic rocks.
The chemical IUPAC name is iron(II,III) oxide and the common chemical name is ferrous-ferric oxide. (Full article...) -
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Cleavage, in mineralogy and materials science, is the tendency of crystalline materials to split along definite crystallographic structural planes. These planes of relative weakness are a result of the regular locations of atoms and ions in the crystal, which create smooth repeating surfaces that are visible both in the microscope and to the naked eye. If bonds in certain directions are weaker than others, the crystal will tend to split along the weakly bonded planes. These flat breaks are termed "cleavage". The classic example of cleavage is mica, which cleaves in a single direction along the basal pinacoid, making the layers seem like pages in a book. In fact, mineralogists often refer to "books of mica".
Diamond and graphite provide examples of cleavage. Each is composed solely of a single element, carbon. In diamond, each carbon atom is bonded to four others in a tetrahedral pattern with short covalent bonds. The planes of weakness (cleavage planes) in a diamond are in four directions, following the faces of the octahedron. In graphite, carbon atoms are contained in layers in a hexagonal pattern where the covalent bonds are shorter (and thus even stronger) than those of diamond. However, each layer is connected to the other with a longer and much weaker van der Waals bond. This gives graphite a single direction of cleavage, parallel to the basal pinacoid. So weak is this bond that it is broken with little force, giving graphite a slippery feel as layers shear apart. As a result, graphite makes an excellent dry lubricant.
While all single crystals will show some tendency to split along atomic planes in their crystal structure, if the differences between one direction or another are not large enough, the mineral will not display cleavage. Corundum, for example, displays no cleavage. (Full article...) -
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Sapphire is a precious gemstone, a variety of the mineral corundum, consisting of aluminium oxide (α-Al2O3) with trace amounts of elements such as iron, titanium, cobalt, lead, chromium, vanadium, magnesium, boron, and silicon. The name sapphire is derived from the Latin word sapphirus, itself from the Greek word sappheiros (σάπφειρος), which referred to lapis lazuli. It is typically blue, but natural "fancy" sapphires also occur in yellow, purple, orange, and green colors; "parti sapphires" show two or more colors. Red corundum stones also occur, but are called rubies rather than sapphires. Pink-colored corundum may be classified either as ruby or sapphire depending on locale. Commonly, natural sapphires are cut and polished into gemstones and worn in jewelry. They also may be created synthetically in laboratories for industrial or decorative purposes in large crystal boules. Because of the remarkable hardness of sapphires – 9 on the Mohs scale (the third hardest mineral, after diamond at 10 and moissanite at 9.5) – sapphires are also used in some non-ornamental applications, such as infrared optical components, high-durability windows, wristwatch crystals and movement bearings, and very thin electronic wafers, which are used as the insulating substrates of special-purpose solid-state electronics such as integrated circuits and GaN-based blue LEDs. Sapphire is the birthstone for September and the gem of the 45th anniversary. A sapphire jubilee occurs after 65 years. (Full article...) -
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Turquoise is an opaque, blue-to-green mineral that is a hydrous phosphate of copper and aluminium, with the chemical formula CuAl6(PO4)4(OH)8·4H2O. It is rare and valuable in finer grades and has been prized as a gemstone for millennia due to its hue.
Like most other opaque gems, turquoise has been devalued by the introduction of treatments, imitations, and synthetics into the market. The robin egg blue or sky blue color of the Persian turquoise mined near the modern city of Nishapur, Iran, has been used as a guiding reference for evaluating turquoise quality. (Full article...) -
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Cinnabar (/ˈsɪnəˌbɑːr/; from Ancient Greek κιννάβαρι (kinnábari)), or cinnabarite (/ˌsɪnəˈbɑːraɪt/), also known as mercurblende is the bright scarlet to brick-red form of mercury(II) sulfide (HgS). It is the most common source ore for refining elemental mercury and is the historic source for the brilliant red or scarlet pigment termed vermilion and associated red mercury pigments.
Cinnabar generally occurs as a vein-filling mineral associated with volcanic activity and alkaline hot springs. The mineral resembles quartz in symmetry and it exhibits birefringence. Cinnabar has a mean refractive index near 3.2, a hardness between 2.0 and 2.5, and a specific gravity of approximately 8.1. The color and properties derive from a structure that is a hexagonal crystalline lattice belonging to the trigonal crystal system, crystals that sometimes exhibit twinning.
Cinnabar has been used for its color since antiquity in the Near East, including as a rouge-type cosmetic, in the New World since the Olmec culture, and in China since as early as the Yangshao culture, where it was used in coloring stoneware.
Associated modern precautions for the use and handling of cinnabar arise from the toxicity of the mercury component, which was recognized as early as ancient Rome. (Full article...) -
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Diamond is a solid form of the element carbon with its atoms arranged in a crystal structure called diamond cubic. Another solid form of carbon known as graphite is the chemically stable form of carbon at room temperature and pressure, but diamond is metastable and converts to it at a negligible rate under those conditions. Diamond has the highest hardness and thermal conductivity of any natural material, properties that are used in major industrial applications such as cutting and polishing tools. They are also the reason that diamond anvil cells can subject materials to pressures found deep in the Earth.
Because the arrangement of atoms in diamond is extremely rigid, few types of impurity can contaminate it (two exceptions are boron and nitrogen). Small numbers of defects or impurities (about one per million of lattice atoms) can color a diamond blue (boron), yellow (nitrogen), brown (defects), green (radiation exposure), purple, pink, orange, or red. Diamond also has a very high refractive index and a relatively high optical dispersion.
Most natural diamonds have ages between 1 billion and 3.5 billion years. Most were formed at depths between 150 and 250 kilometres (93 and 155 mi) in the Earth's mantle, although a few have come from as deep as 800 kilometres (500 mi). Under high pressure and temperature, carbon-containing fluids dissolved various minerals and replaced them with diamonds. Much more recently (hundreds to tens of million years ago), they were carried to the surface in volcanic eruptions and deposited in igneous rocks known as kimberlites and lamproites.
Synthetic diamonds can be grown from high-purity carbon under high pressures and temperatures or from hydrocarbon gases by chemical vapor deposition (CVD). Imitation diamonds can also be made out of materials such as cubic zirconia and silicon carbide. Natural, synthetic, and imitation diamonds are most commonly distinguished using optical techniques or thermal conductivity measurements. (Full article...) -
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Dolomite (/ˈdɒl.əˌmaɪt, ˈdoʊ.lə-/) is an anhydrous carbonate mineral composed of calcium magnesium carbonate, ideally CaMg(CO3)2. The term is also used for a sedimentary carbonate rock composed mostly of the mineral dolomite (see Dolomite (rock)). An alternative name sometimes used for the dolomitic rock type is dolostone. (Full article...) -
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Garnets ( /ˈɡɑːrnɪt/) are a group of silicate minerals that have been used since the Bronze Age as gemstones and abrasives.
All species of garnets possess similar physical properties and crystal forms, but differ in chemical composition. The different species are pyrope, almandine, spessartine, grossular (varieties of which are hessonite or cinnamon-stone and tsavorite), uvarovite and andradite. The garnets make up two solid solution series: pyrope-almandine-spessartine (pyralspite), with the composition range [Mg,Fe,Mn]3Al2(SiO4)3; and uvarovite-grossular-andradite (ugrandite), with the composition range Ca3[Cr,Al,Fe]2(SiO4)3. (Full article...) -
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Graphite (/ˈɡræfaɪt/) is a crystalline form of the element carbon. It consists of stacked layers of graphene. Graphite occurs naturally and is the most stable form of carbon under standard conditions. Synthetic and natural graphite are consumed on a large scale (1.3 million metric tons per year in 2022) for uses in pencils, lubricants, and electrodes. Under high pressures and temperatures it converts to diamond. It is a good (but not excellent) conductor of both heat and electricity. (Full article...)
Selected mineralogist
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Carl Franz Anton Ritter von Schreibers (15 August 1775 – 21 May 1852) was an Austrian naturalist who was a native of Pressburg, Hungary, Habsburg Empire (today Bratislava, Slovakia).
In 1847, an uncommon iron-nickel-phosphide ((Fe,Ni)3P) mineral was named in his honor by Wilhelm Karl Ritter von Haidinger (1775–1871). The mineral is found in meteorites, and is known today as schreibersite. As a zoologist, he was the first to perform a comprehensive anatomical study of the olm, a cave-dwelling, aquatic amphibian. The plant genus Schreibersia (synonym Augusta, family Rubiaceae) was named in his honor by Johann Baptist Emanuel Pohl. The common bent-wing bat (Miniopterus schreibersii), also known as the Schreibers's long-fingered bat or Schreibers's bat, is a species of insectivorous bat. They appear to have dispersed from a subtropical origin and distributed throughout the southern Palearctic, Ethiopic, Oriental, and Australian regions. In Europe, it is present in the southern half on the continent from Iberia to the Caucasus, with the largest populations found in the warmer Mediterranean area. The common and scientific names honor Carl Franz Anton Ritter von Schreibers. (Full article...) -
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Auguste Michel-Lévy (7 August 1844 – 27 September 1911) was a French geologist. He was born in Paris. (Full article...) -
Image 3Friedrich Klockmann (12 April 1858, Schwerin – 17 November 1937, Aachen) was a German geologist and mineralogist.
He studied geology and mineralogy at the Bergakademie in Clausthal and at the University of Rostock, receiving his doctorate in 1881. Following graduation he worked for the Prussian Geological Survey, based in Berlin. From 1887 he taught classes in mineralogy and geology at the academy in Clausthal, and in 1892 attained the title of professor. From 1899 he worked as a professor at the technical university in Aachen, where in 1917/18 he served as academic rector. (Full article...) -
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Harry von Eckermann (1886–1969) was a Swedish industrialist, mineralogist and geologist. His studies were centered around anorogenic alkaline igneous rocks occurring in the Baltic Shield. Following this line he studied the Alnö Complex, Norra Kärr Alkaline Complex and various Rapakivi granites.
In a 1948 publication on Alnö, von Eckermann correctly claimed a magmatic origin of carbonatite, albeit his finds were only widely accepted after the Ol Doinyo Lengai eruption of carbonatite lava in the 1960s showed contemporary evidence on the existence of such magmas. In relation to the mid-20th century granitization controversy von Eckermann rejected the notion that rapakivi granites were Jotnian sediments turned into granite. (Full article...) -
Image 5Rudolf Koechlin (11 November 1862 – 11 February 1939) was an Austrian mineralogist.
Koechlin was born and died in Vienna. He studied mineralogy, crystallography, petrology and geology at the University of Vienna, obtaining his doctorate in 1887 with a thesis on manganite, polianite and pyrolusite. At Vienna, his instructors included Gustav Tschermak and Albrecht Schrauf. In 1884 he began work as a volunteer in the mineralogical-petrography department of the Naturhistorisches Hofmuseum in Vienna. In 1897 he became a "custos-adjunct", later named a curator first-class (1912), and in 1920, was appointed director of the mineralogical-petrography department. (Full article...) -
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Adolph Knopf (December 2, 1882 – November 23, 1966) was an American geologist. Educated at the University of California, Berkeley, he held professional appointments at the United States Geological Survey, Yale University, and Stanford University. He was primarily a petrologist and mineralogist, though later in his career contributed to geochronology. He performed much of his field work in the western United States, investigating mineral deposits in Alaska, the Boulder Batholith in Montana, and the Gold Country of California.
Knopf was a member of the National Academy of Sciences and the American Academy of Arts and Sciences. He served as president of the Geological Society of America in 1944 and received its Penrose Medal in 1959. His second wife, Eleanora Knopf, was a notable geologist and frequent collaborator. (Full article...) -
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Franz Eugen Geinitz (15 February 1854, Dresden – 9 March 1925, Rostock) was a German geologist and mineralogist best known for his geological studies of the Mecklenburg region. He was the son of geologist Hanns Bruno Geinitz. (Full article...) -
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Ernst Friedrich Germar (3 November 1786 – 8 July 1853) was a German professor and director of the Mineralogical Museum at Halle. As well as being a mineralogist he was interested in entomology and particularly in the Coleoptera and Hemiptera. He wrote monographs on several insect families including the Scutelleridae. He also took an interest in paleoentomology. (Full article...) -
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Ernst Erhard Friedrich Wilhelm Schmid (22 May 1815 in Hildburghausen – 16 February 1885 in Jena) was a German paleontologist. He was the son of law professor Karl Ernst Schmid (1774–1852).
He studied natural sciences at the universities of Jena and Vienna, receiving his doctorate in 1839. In 1843 he became an associate professor at Jena, where with Matthias Jakob Schleiden, he founded a physiological institute. At the institute he dealt with subjects that included mineralogy, geology, chemistry and physics. In 1856 he was appointed a professor of natural sciences at the University of Jena. (Full article...) -
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Gaius Plinius Secundus (AD 23/24 – AD 79), called Pliny the Elder (/ˈplɪni/), was a Roman author, naturalist, natural philosopher, naval and army commander of the early Roman Empire, and a friend of the emperor Vespasian. He wrote the encyclopedic Naturalis Historia (Natural History), which became an editorial model for encyclopedias. He spent most of his spare time studying, writing, and investigating natural and geographic phenomena in the field.
Among Pliny's greatest works was the twenty-volume Bella Germaniae ("The History of the German Wars"), which is no longer extant. Bella Germaniae, which began where Aufidius Bassus' Libri Belli Germanici ("The War with the Germans") left off, was used as a source by other prominent Roman historians, including Plutarch, Tacitus, and Suetonius. Tacitus may have used Bella Germaniae as the primary source for his work, De origine et situ Germanorum ("On the Origin and Situation of the Germans"). (Full article...) -
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Thomas Egleston (December 9, 1832 – January 15, 1900) was an American engineer who helped found Columbia University's School of Mines, now the Fu Foundation School of Engineering and Applied Science. Throughout his lifetime, Egleston published numerous lectures and books on metallurgy. Many of his books are preserved today at the archive in the Library of Congress. (Full article...) -
Image 12Jacques-Louis, Comte de Bournon FRS, FGS (21 January 1751 – 24 August 1825) was a French soldier and mineralogist who came to England after the French Revolution. He gained prominence in the scientific community, being elected a fellow of the Royal Society and was a founding member of the Geological Society before returning to France after the Bourbon Restoration. (Full article...)
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Adolf Karl Remelé (17 July 1839, Uerdingen – 16 November 1915, Eberswalde) was a German geologist and mineralogist.
He received his education at the University of Bonn, at the École des Mines in Paris and from the University of Berlin, receiving his doctorate in 1864 with the dissertation "De rubro uranico". In 1867 he qualified as a lecturer at Berlin, and during the following year, succeeded Lothar Meyer at the Forestry Academy in Eberswalde, where he taught classes in chemistry, geognosy and mineralogy. (Full article...) -
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Anders Jahan Retzius (3 October 1742 – 6 October 1821) was a Swedish chemist, botanist and entomologist. (Full article...) -
Image 15Josef Zemann (25 May 1923 – 16 October 2022) was an Austrian mineralogist and geologist. (Full article...)
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Image 16
Ignacy Domeyko or Domejko, pseudonym: Żegota (Spanish: Ignacio Domeyko, Spanish pronunciation: [iɣˈnasjo ðoˈmejko]; 31 July 1802 – 23 January 1889) was a Polish geologist, mineralogist, educator, and founder of the University of Santiago, in Chile. Domeyko spent most of his life, and died, in his adopted country, Chile.
After a youth passed in partitioned Poland, Domeyko participated in the Polish–Russian War 1830–31. Upon Russian victory, he was exiled, spending part of his life in France (where he had gone with a fellow Philomath, Polish poet Adam Mickiewicz) before eventually settling in Chile, whose citizen he became. (Full article...) -
Image 17William Sefton Fyfe, CC FRSC FRS FRSNZ (4 June 1927 – 11 November 2013) was a New Zealand geologist and Professor Emeritus in the department of Earth Sciences at the University of Western Ontario. He is widely considered among the world's most eminent geochemists. (Full article...)
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Image 18Alexander Rose (1781 – 1860) of Edinburgh was a wood and ivory turner, following in the footsteps of his father, John, who came from Cromarty. He developed an interest in minerals and began a mineral collection, becoming a dealer in minerals. He later became a lecturer in geology and mineralogy at Queen's College, Edinburgh and was eventually nominated as a Fellow of the Royal Scottish Academy.
He was educated at the Royal High School and in 1816, he married Isabella Boyne. They had three sons and six daughters. (Full article...) -
Image 19
Gustav von Leonhard (12 November 1816 in Munich – 27 December 1878 in Heidelberg) was a German mineralogist and geologist. He was the son of mineralogist Karl Cäsar von Leonhard.
He studied mineralogy and related sciences at the University of Heidelberg, receiving his doctorate in 1840. He continued his education in Berlin, and in 1841 obtained his habilitation at Heidelberg. In 1853 he became an associate professor of mineralogy at the University of Heidelberg. (Full article...) -
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Louis Jean-Marie Daubenton (29 May 1716 – 1 January 1800) was a French naturalist and contributor to the Encyclopédie ou Dictionnaire raisonné des sciences, des arts et des métiers. (Full article...) -
Image 21Arthur Francis "Bud" Buddington (November 29, 1890 – December 25, 1980) was an American geologist. Born in Wilmington, Delaware, he grew up there and in West Mystic, Connecticut. He was educated at Brown University and Princeton University.
After short stints teaching at Brown and Princeton, serving in the Chemical Warfare Service during World War I, and researching at the Carnegie Institution for Science, Buddington settled at Princeton, where he taught for nearly 40 years. He chaired the Department of Geology from 1936 to 1950. He also had a long career with the U.S. Geological Survey (USGS), doing field work for that agency in Alaska, Oregon, and the northeastern United States. (Full article...) -
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Franz Ernst Brückmann (27 September 1697 – 21 March 1753) was a German mineralogist born at Marienthal near Helmstedt. Having qualified as a physician in 1721, he practised at Braunschweig and afterwards at Wolfenbüttel (from 1728). In 1747 he was appointed medical assessor in Braunschweig.
His leisure time was given up to natural history, and especially to mineralogy and botany. He appears to have been the first to introduce the term "oolithus" to rocks that resemble in structure the roe of a fish; whence the terms "oolite" and "oolitic". He died at Wolfenbüttel. (Full article...) -
Image 23
Hubert Curien (30 October 1924 – 6 February 2005) was a French physicist and a key figure in European science politics, as the President of CERN Council (1994–1996), the first chairman of the European Space Agency (ESA) (1981–1984), and second President of the Academia Europæa and a President of Fondation de France. (Full article...) -
Image 24
Wolfgang Xavier Franz Ritter von Kobell (19 July 1803 – 11 November 1882) was a German mineralogist and writer of short stories and poems in Bavarian dialect. (Full article...) -
Image 25
Alexander Filippovich Postels (Russian: Александр Филиппович Постельс; 24 August 1801 Dorpat – 28 June 1871 Vyborg), was a Russian naturalist, mineralogist and artist of Baltic German descent.
Postels studied at St.Petersburg Imperial University and in 1826 lectured there on inorganic chemistry. (Full article...)
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For editor resources and to collaborate with other editors on improving Wikipedia's Minerals-related articles, see WikiProject Rocks and minerals.
General images
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Image 2Sphalerite crystal partially encased in calcite from the Devonian Milwaukee Formation of Wisconsin (from Mineral)
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Image 3Muscovite, a mineral species in the mica group, within the phyllosilicate subclass (from Mineral)
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Image 4Red cinnabar (HgS), a mercury ore, on dolomite. (from Mineral)
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Image 5Pink cubic halite (NaCl; halide class) crystals on a nahcolite matrix (NaHCO3; a carbonate, and mineral form of sodium bicarbonate, used as baking soda). (from Mineral)
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Image 6Gypsum desert rose (from Mineral)
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Image 7Schist is a metamorphic rock characterized by an abundance of platy minerals. In this example, the rock has prominent sillimanite porphyroblasts as large as 3 cm (1.2 in). (from Mineral)
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Image 8Diamond is the hardest natural material, and has a Mohs hardness of 10. (from Mineral)
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Image 10Mohs hardness kit, containing one specimen of each mineral on the ten-point hardness scale (from Mohs scale)
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Image 12Epidote often has a distinctive pistachio-green colour. (from Mineral)
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Image 13Black andradite, an end-member of the orthosilicate garnet group. (from Mineral)
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Image 14Perfect basal cleavage as seen in biotite (black), and good cleavage seen in the matrix (pink orthoclase). (from Mineral)
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Image 15Mohs Scale versus Absolute Hardness (from Mineral)
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Image 16Hübnerite, the manganese-rich end-member of the wolframite series, with minor quartz in the background (from Mineral)
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Image 17Native gold. Rare specimen of stout crystals growing off of a central stalk, size 3.7 x 1.1 x 0.4 cm, from Venezuela. (from Mineral)
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Image 19An example of elbaite, a species of tourmaline, with distinctive colour banding. (from Mineral)
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Image 24When minerals react, the products will sometimes assume the shape of the reagent; the product mineral is termed a pseudomorph of (or after) the reagent. Illustrated here is a pseudomorph of kaolinite after orthoclase. Here, the pseudomorph preserved the Carlsbad twinning common in orthoclase. (from Mineral)
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Image 26Asbestiform tremolite, part of the amphibole group in the inosilicate subclass (from Mineral)
In the news
- 3 May 2024 –
- Panama bans First Quantum Minerals from extracting copper following the closure of its Cobre Panamá mine last year. (Reuters) (The Globe and Mail)
Did you know ...?
- ... that the mineral diaboleite (pictured) was so named out of desperation?
- ... that silicate perovskites may make up to 93% of the lower mantle and that the magnesium form is considered to be Earth's most abundant mineral?
- ... that while huemulite was discovered in 1959, it was not described until 1966?
Subcategories
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Topics
Overview | ||
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Common minerals |
Ore minerals, mineral mixtures and ore deposits | |||||||||
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Ores |
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Deposit types |
Borates | |||||
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Carbonates | |||||
Oxides |
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Phosphates | |||||
Silicates | |||||
Sulfides | |||||
Other |
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Crystalline | |||||||
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Cryptocrystalline | |||||||
Amorphous | |||||||
Miscellaneous | |||||||
Notable varieties |
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Oxide minerals |
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Silicate minerals | |||||
Other |
Gemmological classifications by E. Ya. Kievlenko (1980), updated | |||||||||
Jewelry stones |
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Jewelry-Industrial stones |
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Industrial stones |
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Mineral identification | |
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"Special cases" ("native elements and organic minerals") |
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"Sulfides and oxides" |
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"Evaporites and similars" |
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"Mineral structures with tetrahedral units" (sulfate anion, phosphate anion, silicon, etc.) |
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