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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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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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...) -
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Chalk is a soft, white, porous, sedimentary carbonate rock. It is a form of limestone composed of the mineral calcite and originally formed deep under the sea by the compression of microscopic plankton that had settled to the sea floor. Chalk is common throughout Western Europe, where deposits underlie parts of France, and steep cliffs are often seen where they meet the sea in places such as the Dover cliffs on the Kent coast of the English Channel.
Chalk is mined for use in industry, such as for quicklime, bricks and builder's putty, and in agriculture, for raising pH in soils with high acidity. It is also used for "blackboard chalk" for writing and drawing on various types of surfaces, although these can also be manufactured from other carbonate-based minerals, or gypsum. (Full article...) -
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Talc, or talcum, is a clay mineral composed of hydrated magnesium silicate, with the chemical formula Mg3Si4O10(OH)2. Talc in powdered form, often combined with corn starch, is used as baby powder. This mineral is used as a thickening agent and lubricant. It is an ingredient in ceramics, paints, and roofing material. It is a main ingredient in many cosmetics. It occurs as foliated to fibrous masses, and in an exceptionally rare crystal form. It has a perfect basal cleavage and an uneven flat fracture, and it is foliated with a two-dimensional platy form.
The Mohs scale of mineral hardness, based on scratch hardness comparison, defines value 1 as the hardness of talc, the softest mineral. When scraped on a streak plate, talc produces a white streak, though this indicator is of little importance, because most silicate minerals produce a white streak. Talc is translucent to opaque, with colors ranging from whitish grey to green with a vitreous and pearly luster. Talc is not soluble in water, and is slightly soluble in dilute mineral acids.
Soapstone is a metamorphic rock composed predominantly of talc. (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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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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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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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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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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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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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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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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Gypsum is a soft sulfate mineral composed of calcium sulfate dihydrate, with the chemical formula CaSO4·2H2O. It is widely mined and is used as a fertilizer and as the main constituent in many forms of plaster, drywall and blackboard or sidewalk chalk. Gypsum also crystallizes as translucent crystals of selenite. It forms as an evaporite mineral and as a hydration product of anhydrite. The Mohs scale of mineral hardness defines gypsum as hardness value 2 based on scratch hardness comparison.
Fine-grained white or lightly tinted forms of gypsum known as alabaster have been used for sculpture by many cultures including Ancient Egypt, Mesopotamia, Ancient Rome, the Byzantine Empire, and the Nottingham alabasters of Medieval England. (Full article...) -
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Borax (also referred to as sodium borate, tincal (/ˈtɪŋkəl/) and tincar (/ˈtɪŋkər/)) is a salt (ionic compound), a hydrated or anhydrous borate of sodium, with the chemical formula Na2H20B4O17 (also written as Na2B4O7·10H2O).
It is a colorless crystalline solid that dissolves in water to make a basic solution.
It is commonly available in powder or granular form and has many industrial and household uses, including as a pesticide, as a metal soldering flux, as a component of glass, enamel, and pottery glazes, for tanning of skins and hides, for artificial aging of wood, as a preservative against wood fungus, and as a pharmaceutic alkalizer. In chemical laboratories, it is used as a buffering agent.
The terms tincal and tincar refer to native borax, historically mined from dry lake beds in various parts of Asia. (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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Amethyst is a violet variety of quartz. The name comes from the Koine Greek αμέθυστος amethystos from α- a-, "not" and μεθύσκω (Ancient Greek) methysko / μεθώ metho (Modern Greek), "intoxicate", a reference to the belief that the stone protected its owner from drunkenness. Ancient Greeks wore amethyst and carved drinking vessels from it in the belief that it would prevent intoxication.
Amethyst, a semiprecious stone, is often used in jewelry. (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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Zircon (/ˈzɜːrkɒn, -kən/) is a mineral belonging to the group of nesosilicates and is a source of the metal zirconium. Its chemical name is zirconium(IV) silicate, and its corresponding chemical formula is ZrSiO4. An empirical formula showing some of the range of substitution in zircon is (Zr1–y, REEy)(SiO4)1–x(OH)4x–y. Zircon precipitates from silicate melts and has relatively high concentrations of high field strength incompatible elements. For example, hafnium is almost always present in quantities ranging from 1 to 4%. The crystal structure of zircon is tetragonal crystal system. The natural color of zircon varies between colorless, yellow-golden, red, brown, blue, and green.
The name derives from the Persian zargun, meaning "gold-hued". This word is changed into "jargoon", a term applied to light-colored zircons. The English word "zircon" is derived from Zirkon, which is the German adaptation of this word. Yellow, orange, and red zircon is also known as "hyacinth", from the flower hyacinthus, whose name is of Ancient Greek origin. (Full article...) -
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A ruby is a pinkish red to blood-red colored gemstone, a variety of the mineral corundum (aluminium oxide). Ruby is one of the most popular traditional jewelry gems and is very durable. Other varieties of gem-quality corundum are called sapphires. Ruby is one of the traditional cardinal gems, alongside amethyst, sapphire, emerald, and diamond. The word ruby comes from ruber, Latin for red. The color of a ruby is due to the element chromium.
Some gemstones that are popularly or historically called rubies, such as the Black Prince's Ruby in the British Imperial State Crown, are actually spinels. These were once known as "Balas rubies".
The quality of a ruby is determined by its color, cut, and clarity, which, along with carat weight, affect its value. The brightest and most valuable shade of red, called blood-red or pigeon blood, commands a large premium over other rubies of similar quality. After color follows clarity: similar to diamonds, a clear stone will command a premium, but a ruby without any needle-like rutile inclusions may indicate that the stone has been treated. Ruby is the traditional birthstone for July and is usually pinker than garnet, although some rhodolite garnets have a similar pinkish hue to most rubies. The world's most valuable ruby to be sold at auction is the Sunrise Ruby. (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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Quartz is a hard, crystalline mineral composed of silica (silicon dioxide). The atoms are linked in a continuous framework of SiO4 silicon–oxygen tetrahedra, with each oxygen being shared between two tetrahedra, giving an overall chemical formula of SiO2. Quartz is, therefore, classified structurally as a framework silicate mineral and compositionally as an oxide mineral. Quartz is the second most abundant mineral in Earth's continental crust, behind feldspar.
Quartz exists in two forms, the normal α-quartz and the high-temperature β-quartz, both of which are chiral. The transformation from α-quartz to β-quartz takes place abruptly at 573 °C (846 K; 1,063 °F). Since the transformation is accompanied by a significant change in volume, it can easily induce microfracturing of ceramics or rocks passing through this temperature threshold.
There are many different varieties of quartz, several of which are classified as gemstones. Since antiquity, varieties of quartz have been the most commonly used minerals in the making of jewelry and hardstone carvings, especially in Europe and Asia.
Quartz is the mineral defining the value of 7 on the Mohs scale of hardness, a qualitative scratch method for determining the hardness of a material to abrasion. (Full article...) -
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Galena, also called lead glance, is the natural mineral form of lead(II) sulfide (PbS). It is the most important ore of lead and an important source of silver.
Galena is one of the most abundant and widely distributed sulfide minerals. It crystallizes in the cubic crystal system often showing octahedral forms. It is often associated with the minerals sphalerite, calcite and fluorite. (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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Zeolite is a family of several microporous, crystalline aluminosilicate materials commonly used as commercial adsorbents and catalysts. They mainly consist of silicon, aluminium, oxygen, and have the general formula Mn+
1/n(AlO
2)−
(SiO
2)
x・yH
2O where Mn+
1/n is either a metal ion or H+. These positive ions can be exchanged for others in a contacting electrolyte solution. H+
exchanged zeolites are particularly useful as solid acid catalysts.
The term was originally coined in 1756 by Swedish mineralogist Axel Fredrik Cronstedt, who observed that rapidly heating a material, believed to have been stilbite, produced large amounts of steam from water that had been adsorbed by the material. Based on this, he called the material zeolite, from the Greek ζέω (zéō), meaning "to boil" and λίθος (líthos), meaning "stone".
Zeolites occur naturally, but are also produced industrially on a large scale. , 253 unique zeolite frameworks have been identified, and over 40 naturally occurring zeolite frameworks are known. Every new zeolite structure that is obtained is examined by the International Zeolite Association Structure Commission (IZA-SC) and receives a three-letter designation. (Full article...)
Selected mineralogist
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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 monographed the heteropteran family Scutelleridae.
In 1845, he was elected a foreign member of the Royal Swedish Academy of Sciences. (Full article...) -
Image 2Eugène Louis Melchior Patrin (3 April 1742, Lyon – 15 August 1815, Saint-Vallier) was a French mineralogist and naturalist.
Following two years of travels in Germany, Hungary and Poland, he spent eight years in Russia (Siberia) (1780–87), conducting geological and botanical investigations. He extensively travelled the Urals, the Altai Mountains and other areas of Siberia, with his mineral collections being shipped back to St. Petersburg ahead of his return. This material, however, was partially confiscated by Pyotr Simon Pallas, who kept the best items for his personal cabinet. Patrin's remaining pieces were subsequently offered to the Jardin du Roi collection in Paris, provided that the group not be broken up. In 1804 he was appointed first librarian of the Conseil des mines. From 1790 to 1815, he was a member of the Académie des sciences, belles-lettres et arts de Lyon. (Full article...) -
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Frank Christopher Hawthorne CC FRSC (born 8 January 1946 in Bristol, England) is a Canadian mineralogist, crystallographer and spectroscopist. He works at the University of Manitoba, Winnipeg, Manitoba, Canada, and is currently Distinguished Professor Emeritus. By combining Graph Theory, Bond-Valence Theory and the moments approach to the electronic energy density of solids he has developed Bond Topology
as a rigorous approach to understanding the atomic arrangements, chemical compositions and paragenesis of complex oxide and oxysalt minerals. (Full article...) -
Image 4Gustaf Flink, born 18 January 1848 in Ås Parish, Skaraborg County, died 11 January 1931, was a Swedish mineralogist.
Flink received training as a primary school teacher and graduated in Gothenburg in 1869. In 1871 he received a teaching position in Stockholm. He accompanied Adolf Erik Nordenskiöld on his expedition to Greenland, during which he collected minerals and petrified plants on Iceland in 1883. He returned to Iceland in 1893. On behalf of a Royal Danish geological and geographical commission he made mineralogical investigations in southern Greenland in 1897. (Full article...) -
Image 5Anselmus de Boodt or Anselmus Boetius de Boodt (Bruges, 1550 - Bruges, 21 June 1632) was a Flemish humanist naturalist, Rudolf II physician's gemologist. Along with the German known as Georgius Agricola with mineralogy, de Boodt was responsible for establishing modern gemology. De Boodt was an avid gems and minerals collector who travelled widely to various mining regions in Belgium, Germany, Bohemia and Silesia to collect samples. His definitive work on the subject was the Gemmarum et Lapidum Historia (1609).
De Boodt was also a gifted draughtsman who made many natural history illustrations and developed a natural history taxonomy. (Full article...) -
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John Mawe (1764 – 26 October 1829) was a British mineralogist who became known for his practical approach to the discipline. (Full article...) -
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Evgraf Stepanovich Fedorov (Russian: Евгра́ф Степа́нович Фёдоров, 22 December [O.S. 10 December] 1853 – 21 May 1919) was a Russian mathematician, crystallographer and mineralogist.
Fedorov was born in the Russian city of Orenburg. His father was a topographical engineer. The family later moved to Saint Petersburg. From the age of fifteen, he was deeply interested in the theory of polytopes, which later became his main research interest. He was a distinguished graduate of the Gorny Institute, which he joined at the age of 26. He was elected the first Director of the Institute in 1905. (Full article...) -
Image 8Warren D. Huff (born April 16, 1937) is Professor of Geology at the University of Cincinnati (UC). He specializes in clay mineralogy, researching the remnants of ancient volcanic eruptions.
He received his BA from Harvard College, 1959 and his PhD from University of Cincinnati, 1963. He has served as assistant professor at UC 1963-1969, associate professor 1969-1985, full professor 1985 to date. He teaches introductory geology sequence. (Full article...) -
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Berend George Escher (4 April 1885 – 11 October 1967) was a Dutch geologist.
Escher had a broad interest, but his research was mainly on crystallography, mineralogy and volcanology. He was a pioneer in experimental geology. He was a half-brother of the artist M. C. Escher, and had some influence on his work due to his knowledge of crystallography. M.C. Escher created a woodcut ex libris for his brother 'Beer' with a stylized image of a volcano around 1922 (Bool number 91). (Full article...) -
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Carl Ernst Arthur Wichmann (9 April 1851 in Hamburg – 28 November 1927 in Hamburg) was a German geologist and mineralogist. He was professor in geology at Utrecht University from 1879 to 1921, where he founded the geological institute. His daughter was the jurist and anarchist-socialist Clara Wichmann, his son the artist and fascist Erich Wichmann.
Arthur Wichmann spent his youth in Hamburg, where his father ran a boarding school. From 1871 to 1874 he studied at Leipzig University, where he was a pupil of Ferdinand Zirkel, from whom he got his interest in mineralogy. After he spent a few years as assistant to Zirkel he became professor at Utrecht University. (Full article...) -
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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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Alice Mary Dowse Weeks (August 26, 1909 – August 29, 1988) was an American geologist. Weeksite is named after her. She identified uranophane in 1953 along with Mary E. Thompson. Weeks was the first to propose the concept of oxidation of ore deposits that contain uranium, vanadium, and other accessory metals. She founded the Geology Department at Temple University in Philadelphia, and was a strong proponent of women in geology. (Full article...) -
Image 13Hendrik Enno Boeke (12 September 1881, in Wormerveer – 6 December 1918, in Frankfurt am Main) was a Dutch mineralogist and petrographer.
From 1900 he studied chemistry and physics at the University of Amsterdam, where his instructors included Hendrik Willem Bakhuis Roozeboom and Johannes Diderik van der Waals. He then worked as an assistant under Gustav Tammann in Göttingen and to Friedrich Rinne at the Technical University of Hannover. In 1909 he became a lecturer of chemistry at the University of Königsberg, and during the following year, an associate professor of physical-chemical mineralogy and petrology at the University of Leipzig. (Full article...) -
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Edward Daniel Clarke (5 June 1769 – 9 March 1822) was an English clergyman, naturalist, mineralogist, and traveller. (Full article...) -
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Johann Friedrich Ludwig Hausmann (22 February 1782, Hannover – 26 December 1859, Göttingen) was a German mineralogist. (Full article...) -
Image 16Wolf Jürgen Baron von Engelhardt (9 February 1910, Tartu – 4 December 2008, Tübingen) was a German geologist and mineralogist.
Baron von Engelhardt was a descendant of a Baltic German noble family Engelhardt. (Full article...) -
Image 17Peggy-Kay Hamilton (1922–1959) was born in Illinois in 1922 and was an American Research Associate in Mineralogy in the Department of Geology at Columbia University. One of Hamilton's first research breakthroughs was developing Research Project 49, otherwise known as the study of clay minerals. In her later research years, her focus shifted and led to her becoming involved full time in the study of uranium.
Hamilton achieved success in the fields of geology and mineralogy; according to her frequent research partner and friend Paul F. Kerr, Hamilton was held in high regard by both students at Columbia University as well as professional colleagues at multiple scientific research institutions. (Full article...) -
Image 18Martine de Bertereau, also known as Baroness de Beausoleil, (c. 1600 – after 1642) was the first recorded female mineralogist as well as mining engineer along with her husband, Jean de Chastelet. She traveled extensively throughout Europe in search of mineral deposits and fresh ground water under the employment of various nobles and royals. During the reign of the French King, Louis XIII, Martine and her husband surveyed the sites of potential mines in France. During one of their mining expeditions Martine and her family were accused of witchcraft and fled to Hungary. Later, Martine, her husband and oldest daughter were arrested and eventually died in prison sometime after 1642. During her life, she produced multiple pieces of literature derived largely from the Roman engineer Vitruvius's book on architecture, De architectura. Her writings describe the use of divining-rods, similar to dowsing, as well as other renowned scientific ideas. Martine de Bertereau was not forthcoming about her use of different scientific ideas, and preferred the public to believe she was using magic, or renowned ancient scientific ideas. Her success came from her development in the understanding of the geologic world around her. It is uncertain of her reasoning behind the decision to lie about her actual means of success. Her literature provides a unique glimpse into the craft and skills required to mine in the seventeenth century. (Full article...)
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Karl Rössler (6 May 1788, in Wiesbaden – 23 August 1863, in Hanau) was a German manufacturer and mineralogist.
After a business apprenticeship in Frankfurt am Main, he acquired in 1818 a hat factory, which he transformed into a highly successful company. He had a keen interest in the geology, mineralogy and paleontology of the Wetterau, and accordingly, collected numerous minerals and fossils of the region. During his career, he worked closely with geologist Leopold von Buch. (Full article...) -
Image 20Sjur Aasmundsen Sexe (14 August 1808 – 17 February 1888) was a Norwegian mineralogist and educator. (Full article...)
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Image 21Carlo Perrier (born July 7, 1886, in Turin, † May 22, 1948 in Genoa ) was an Italian mineralogist and chemist who did extensive research on the element technetium. With the discovery of technetium in 1937, he and Emilio Segrè accounted for the last gap in the periodic table. Technetium was the first element produced artificially (hence the name that Segrè and Perrier gave it).
His parents were named Bertolini. Perrier studied chemistry at the Polytechnic in Turin with a Laureate degree in 1908. From 1911 to 1912 he worked at the Laboratory for Physical Chemistry and Electrochemistry at ETH Zurich with Baur and Treadwell. He then worked as an assistant of Arnaldo Piutti at the University of Naples. There he made friends with Ferruccio Zambonini and involved with mineralogy and the study of radioactivity. He was Zambonini's assistant in Turin and, after a competition, became director of the State Geochemical Laboratory in Rome in 1921. In 1927 he completed his habilitation and after another competition became an associate professor in Messina. In 1929 he relocated to Palermo and in 1939 to the University of Genoa. (Full article...) -
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Alphonse Francois Renard (27 September 1842 – 9 July 1903), Belgian geologist and petrographer, was born at Ronse, in East Flanders, on 27 September 1842. He was educated for the church of Rome, and from 1866 to 1869 he was superintendent at the college de la Paix, Namur.
In 1870 he entered the Jesuit Training College at the old abbey of Maria Laach in the Eifel, and there, while engaged in studying philosophy and science, he became interested in the geology of the district, and especially in the volcanic rocks. Thenceforth he worked at chemistry and mineralogy, and qualified himself for those petrographical researches for which he was distinguished. (Full article...) -
Image 23Ferruccio Zambonini (17 December 1880 – 12 January 1932) was an Italian mineralogist and geologist. Most of his time he worked on the geology and mineralogy of Mount Vesuvius. (Full article...)
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Image 24
Norman Levi Bowen FRS (June 21, 1887 – September 11, 1956) was a Canadian geologist. Bowen "revolutionized experimental petrology and our understanding of mineral crystallization". Beginning geology students are familiar with Bowen's reaction series depicting how different minerals crystallize under varying pressures and temperatures." (Full article...) -
Image 25
Arthur Aikin FLS FGS (19 May 1773 – 15 April 1854) was an English chemist, mineralogist and scientific writer, and was a founding member of the Chemical Society (now the Royal Society of Chemistry). He first became its treasurer in 1841, and later became the society's second president. (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 1Epidote often has a distinctive pistachio-green colour. (from Mineral)
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Image 2Pink 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 3Black andradite, an end-member of the orthosilicate garnet group. (from Mineral)
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Image 5Muscovite, a mineral species in the mica group, within the phyllosilicate subclass (from Mineral)
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Image 7Diamond is the hardest natural material, and has a Mohs hardness of 10. (from Mineral)
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Image 8Asbestiform tremolite, part of the amphibole group in the inosilicate subclass (from Mineral)
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Image 10Perfect basal cleavage as seen in biotite (black), and good cleavage seen in the matrix (pink orthoclase). (from Mineral)
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Image 11Sphalerite crystal partially encased in calcite from the Devonian Milwaukee Formation of Wisconsin (from Mineral)
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Image 12Mohs hardness kit, containing one specimen of each mineral on the ten-point hardness scale (from Mohs scale)
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Image 13Native 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 14When 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 15Red cinnabar (HgS), a mercury ore, on dolomite. (from Mineral)
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Image 18Hübnerite, the manganese-rich end-member of the wolframite series, with minor quartz in the background (from Mineral)
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Image 20An example of elbaite, a species of tourmaline, with distinctive colour banding. (from Mineral)
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Image 21Schist 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 23Mohs Scale versus Absolute Hardness (from Mineral)
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Image 24Gypsum desert rose (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 leonite (pictured) has been found on Mars?
- ...that crystals of Paulingite, a rare zeolite mineral found in vesicles in the basaltic rocks from the Columbia River, form a perfect clear rhombic dodecahedron?
- ... that abernathyite is both fluorescent and radioactive and is named for the mine operator who discovered it?
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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