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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Image 1
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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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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Crystallography is the experimental science of determining the arrangement of atoms in crystalline solids. Crystallography is a fundamental subject in the fields of materials science and solid-state physics (condensed matter physics). The word crystallography is derived from the Ancient Greek word κρύσταλλος (krústallos; "clear ice, rock-crystal"), and γράφειν (gráphein; "to write"). In July 2012, the United Nations recognised the importance of the science of crystallography by proclaiming that 2014 the International Year of Crystallography. (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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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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Hematite (/ˈhiːməˌtaɪt, ˈhɛmə-/), also spelled as haematite, is a common iron oxide compound with the formula, Fe2O3 and is widely found in rocks and soils. Hematite crystals belong to the rhombohedral lattice system which is designated the alpha polymorph of Fe
2O
3. It has the same crystal structure as corundum (Al
2O
3) and ilmenite (FeTiO
3). With this it forms a complete solid solution at temperatures above 950 °C (1,740 °F).
Hematite naturally occurs in black to steel or silver-gray, brown to reddish-brown, or red colors. It is mined as an important ore mineral of iron. It is electrically conductive. Hematite varieties include kidney ore, martite (pseudomorphs after magnetite), iron rose and specularite (specular hematite). While these forms vary, they all have a rust-red streak. Hematite is not only harder than pure iron, but also much more brittle. Maghemite is a polymorph of hematite (γ-Fe
2O
3) with the same chemical formula, but with a spinel structure like magnetite.
Large deposits of hematite are found in banded iron formations. Gray hematite is typically found in places that have still, standing water or mineral hot springs, such as those in Yellowstone National Park in North America. The mineral can precipitate in the water and collect in layers at the bottom of the lake, spring, or other standing water. Hematite can also occur in the absence of water, usually as the result of volcanic activity.
Clay-sized hematite crystals can also occur as a secondary mineral formed by weathering processes in soil, and along with other iron oxides or oxyhydroxides such as goethite, which is responsible for the red color of many tropical, ancient, or otherwise highly weathered soils. (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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Asbestos (/æsˈbɛstəs, æz-, -tɒs/ ass-BES-təs, az-, -toss) is a naturally occurring fibrous silicate mineral. There are six types, all of which are composed of long and thin fibrous crystals, each fibre (particulate with length substantially greater than width) being composed of many microscopic "fibrils" that can be released into the atmosphere by abrasion and other processes. Inhalation of asbestos fibres can lead to various dangerous lung conditions, including mesothelioma, asbestosis, and lung cancer. As a result of these health effects, asbestos is considered a serious health and safety hazard.
Archaeological studies have found evidence of asbestos being used as far back as the Stone Age to strengthen ceramic pots, but large-scale mining began at the end of the 19th century when manufacturers and builders began using asbestos for its desirable physical properties. Asbestos is an excellent thermal and electrical insulator, and is highly fire resistant, so for much of the 20th century, it was very commonly used across the world as a building material (particularly for its fire-retardant properties), until its adverse effects on human health were more widely recognized and acknowledged in the 1970s. Many buildings constructed before the 1980s contain asbestos.
The use of asbestos for construction and fireproofing has been made illegal in many countries. Despite this, at least 100,000 people are thought to die each year from diseases related to asbestos exposure.[citation needed] In part, this is because many older buildings still contain asbestos; in addition, the consequences of exposure can take decades to arise. The latency period (from exposure to the diagnosis of negative health effects) is typically 20 years. The most common diseases associated with chronic asbestos exposure are asbestosis (scarring of the lungs due to asbestos inhalation) and mesothelioma (a type of cancer).
Many developing countries still support the use of asbestos as a building material, and mining of asbestos is ongoing, with the top producer, Russia, having an estimated production of 790,000 tonnes in 2020. (Full article...) -
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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...) -
Image 10
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...) -
Image 11
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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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...) -
Image 13
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...) -
Image 14
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...) -
Image 15
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...) -
Image 16
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...) -
Image 17
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...) -
Image 18
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...) -
Image 19
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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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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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...) -
Image 22
In crystallography, crystal structure is a description of the ordered arrangement of atoms, ions, or molecules in a crystalline material. Ordered structures occur from the intrinsic nature of the constituent particles to form symmetric patterns that repeat along the principal directions of three-dimensional space in matter.
The smallest group of particles in the material that constitutes this repeating pattern is the unit cell of the structure. The unit cell completely reflects the symmetry and structure of the entire crystal, which is built up by repetitive translation of the unit cell along its principal axes. The translation vectors define the nodes of the Bravais lattice.
The lengths of the principal axes, or edges, of the unit cell and the angles between them are the lattice constants, also called lattice parameters or cell parameters. The symmetry properties of the crystal are described by the concept of space groups. All possible symmetric arrangements of particles in three-dimensional space may be described by the 230 space groups.
The crystal structure and symmetry play a critical role in determining many physical properties, such as cleavage, electronic band structure, and optical transparency. (Full article...) -
Image 23
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...) -
Image 24
Andesite (/ˈændəzaɪt/) is a volcanic rock of intermediate composition. In a general sense, it is the intermediate type between silica-poor basalt and silica-rich rhyolite. It is fine-grained (aphanitic) to porphyritic in texture, and is composed predominantly of sodium-rich plagioclase plus pyroxene or hornblende.
Andesite is the extrusive equivalent of plutonic diorite. Characteristic of subduction zones, andesite represents the dominant rock type in island arcs. The average composition of the continental crust is andesitic. Along with basalts, andesites are a component of the Martian crust.
The name andesite is derived from the Andes mountain range, where this rock type is found in abundance. It was first applied by Christian Leopold von Buch in 1826. (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...)
Selected mineralogist
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Image 1Anselmus 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...) -
Image 2Walter Flight (21 January 1841 – 4 November 1885), was an English mineralogist who studied the chemical composition of meteorites. He published academic papers on the chemical composition of meteorites in both Germany and the United Kingdom. He also worked for the British Museum, the Royal Military Academy, Woolwich, and on a committee appointed by the British Science Association, then known as the British Association. (Full article...)
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Image 3
Eilhard Mitscherlich (German pronunciation: [ˈaɪ̯lhaʁt ˈmɪtʃɐlɪç]; 7 January 1794 – 28 August 1863) was a German chemist, who is perhaps best remembered today for his discovery of the phenomenon of crystallographic isomorphism in 1819. (Full article...) -
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Frederick Augustus Ludwig Karl Wilhelm Genth (May 17, 1820 – February 2, 1893) was a German-American chemist, specializing in analytical chemistry and mineralogy. (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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Hanns Bruno Geinitz (16 October 1814 – 28 January 1900) was a German geologist, born at Altenburg, the capital of Saxe-Altenburg. (Full article...) -
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Johann Friedrich Christian Hessel (27 April 1796 – 3 June 1872) was a German physician (MD, University of Würzburg, 1817) and professor of mineralogy (PhD, University of Heidelberg, 1821) at the University of Marburg. (Full article...) -
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Philip Rashleigh FRS FSA (28 December 1729 – 26 June 1811) of Menabilly, Cornwall, was an antiquary and Fellow of the Royal Society and a Cornish squire. He collected and published the Trewhiddle Hoard of Anglo-Saxon treasure, which still gives its name to the "Trewhiddle style" of 9th century decoration. (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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George Shirley Switzer (June 11, 1915 – March 23, 2008) was an American mineralogist who is credited with starting the Smithsonian Institution's famed National Gem and Mineral Collection by acquiring the Hope Diamond for the museum in 1958. Switzer made the arrangements when renowned New York City jeweler Harry Winston decided to donate the Hope Diamond to the Smithsonian.
Switzer was also known for his analysis of Moon rocks which were brought back by NASA missions to the Moon. (Full article...) -
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Joseph Henry Collins FGS, (16 March 1841 – 12 April 1916) was a British mining engineer, mineralogist and geologist. He died at his home, Crinnis House, near St Austell, on 12 April 1916 and is buried in Campdowns cemetery, Charlestown. (Full article...) -
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George Gibbs (January 7, 1776 – August 6, 1833) was an American mineralogist and mineral collector. The mineral gibbsite is named after him. (Full article...) -
Image 13Stanley Hay Umphray Bowie FRS (born 24 March 1917, in Bixter, Shetland - died 3 September 2008) was a Scottish geologist. He was considered a "world authority on uranium geology and a leader in the field of geochemistry and mineralogy". He developed methods and tools to identify opaque minerals using micro-indentation hardness and optical reflectance. He worked for the British Geological Survey between 1946 and 1977. The mineral bowieite was so named in recognition of his work on identification of opaque minerals. (Full article...)
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Image 14
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...) -
Image 15Aristides Brezina (4 May 1848 – 25 May 1909) was an Austrian mineralogist born in Vienna.
In 1872 he graduated from the University of Tübingen, and afterwards taught crystallography at the University of Vienna. In 1878 he succeeded Austrian mineralogist Gustav Tschermak (1836-1927) as custodian of the meteorite collection at Vienna, and from 1889 until 1896 he was director of the Mineralogisch-Petrographische Abteilung (Department of Mineralogy-Petrography). In 1886, he was elected as a member to the American Philosophical Society. (Full article...) -
Image 16Carlo 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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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...) -
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Johan Georg Forchhammer (26 July 1794 – 14 December 1865) was a Danish mineralogist and geologist. (Full article...) -
Image 19Sjur Aasmundsen Sexe (14 August 1808 – 17 February 1888) was a Norwegian mineralogist and educator. (Full article...)
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Johann Friedrich August Breithaupt (May 16, 1791 – September 22, 1873) was a German mineralogist and professor at Freiberg Mining Academy in Freiberg, Saxony. (Full article...) -
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Hermann Traube (September 24, 1860 – January 29, 1913) was a German mineralogist born in Ratibor, Silesia (presently Racibórz, Poland). He was the son of chemist Moritz Traube (1826–1894).
He studied at the Universities of Leipzig, Heidelberg, Breslau and Greifswald, earning his doctorate in 1884. At Breslau his instructors were Ferdinand Cohn (1828–1898) and Theodor Poleck (1821–1906). (Full article...) -
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Henry Carvill Lewis (November 16, 1853 – July 21, 1888) was an American geologist and mineralogist. (Full article...) -
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Linus Carl Pauling FRS (/ˈpɔːlɪŋ/ PAW-ling; February 28, 1901 – August 19, 1994) was an American chemist, biochemist, chemical engineer, peace activist, author, and educator. He published more than 1,200 papers and books, of which about 850 dealt with scientific topics. New Scientist called him one of the 20 greatest scientists of all time. For his scientific work, Pauling was awarded the Nobel Prize in Chemistry in 1954. For his peace activism, he was awarded the Nobel Peace Prize in 1962. He is one of five people to have won more than one Nobel Prize (the others being Marie Curie, John Bardeen, Frederick Sanger, and Karl Barry Sharpless). Of these, he is the only person to have been awarded two unshared Nobel Prizes, and one of two people to be awarded Nobel Prizes in different fields, the other being Marie Curie.
Pauling was one of the founders of the fields of quantum chemistry and molecular biology. His contributions to the theory of the chemical bond include the concept of orbital hybridisation and the first accurate scale of electronegativities of the elements. Pauling also worked on the structures of biological molecules, and showed the importance of the alpha helix and beta sheet in protein secondary structure. Pauling's approach combined methods and results from X-ray crystallography, molecular model building, and quantum chemistry. His discoveries inspired the work of Rosalind Franklin, James Watson, Francis Crick, and Maurice Wilkins on the structure of DNA, which in turn made it possible for geneticists to crack the DNA code of all organisms. (Full article...) -
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William Babington FRS FGS (21 May 1756 – 29 April 1833) was an Anglo-Irish physician and mineralogist. (Full article...) -
Image 25Jacques-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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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 2Gypsum desert rose (from Mineral)
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Image 3Epidote often has a distinctive pistachio-green colour. (from Mineral)
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Image 6An example of elbaite, a species of tourmaline, with distinctive colour banding. (from Mineral)
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Image 8Hübnerite, the manganese-rich end-member of the wolframite series, with minor quartz in the background (from Mineral)
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Image 10When 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 11Schist 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 12Pink 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 13Red cinnabar (HgS), a mercury ore, on dolomite. (from Mineral)
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Image 14Mohs hardness kit, containing one specimen of each mineral on the ten-point hardness scale (from Mohs scale)
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Image 15Native 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 16Perfect basal cleavage as seen in biotite (black), and good cleavage seen in the matrix (pink orthoclase). (from Mineral)
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Image 17Diamond is the hardest natural material, and has a Mohs hardness of 10. (from Mineral)
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Image 19Sphalerite crystal partially encased in calcite from the Devonian Milwaukee Formation of Wisconsin (from Mineral)
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Image 20Asbestiform tremolite, part of the amphibole group in the inosilicate subclass (from Mineral)
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Image 21Black andradite, an end-member of the orthosilicate garnet group. (from Mineral)
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Image 25Mohs Scale versus Absolute Hardness (from Mineral)
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Image 26Muscovite, a mineral species in the mica group, within the phyllosilicate 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 after a mine tunnel was dug near Cerro de Pasco, Peru, the first known specimen of pascoite (example pictured) formed on the walls?
- ... that the name of mineral scrutinyite reflects the efforts spent to distinguish it from plattnerite – another form of lead dioxide?
- ... that the crystal symmetry of melanophlogite changes depending on the guests trapped inside it?
- ... that the mineral messelite was described in 1890, discredited in 1940, reinstated and named neomesselite in 1955, and named messelite once again by 1959?
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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