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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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 2
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...) - Image 3
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 (albeit there are many exceptions). (Full article...) - Image 4
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 5
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...) - Image 6
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 would be the International Year of Crystallography.
Before the development of X-ray diffraction and X-ray crystallography (see below), the study of crystals was based on physical measurements of their geometry using a goniometer. This involved measuring the angles of crystal faces relative to each other and to theoretical reference axes (crystallographic axes), and establishing the symmetry of the crystal in question. The position in 3D space of each crystal face is plotted on a stereographic net such as a Wulff net or Lambert net. The pole to each face is plotted on the net. Each point is labelled with its Miller index. The final plot allows the symmetry of the crystal to be established.
Crystallographic methods depend mainly on analysis of the diffraction patterns of a sample targeted by a beam of some type. X-rays are most commonly used; other beams used include electrons or neutrons. Crystallographers often explicitly state the type of beam used, as in the terms X-ray crystallography, neutron diffraction and electron diffraction. These three types of radiation interact with the specimen in different ways.- X-rays interact with the spatial distribution of electrons in the sample.
- Neutrons are scattered by the atomic nuclei through the strong nuclear forces, but in addition, the magnetic moment of neutrons is non-zero. They are therefore also scattered by magnetic fields. When neutrons are scattered from hydrogen-containing materials, they produce diffraction patterns with high noise levels. However, the material can sometimes be treated to substitute deuterium for hydrogen. Because of these different forms of interaction, the three types of radiation are suitable for different crystallographic studies.
- Electrons are charged particles and therefore interact with the total charge distribution of both the atomic nuclei and the electrons of the sample.
It is hard to focus x-rays or neutrons, but since electrons are charged they can be focused and are used in electron microscope to produce magnified images. There are many ways that transmission electron microscopy and related techniques such as scanning transmission electron microscopy, high-resolution electron microscopy can be used to obtain images with in many cases atomic resolution from which crystallographic information can be obtained. There are also other methods such as low-energy electron diffraction, low-energy electron microscopy and reflection high-energy electron diffraction which can be used to obtain crystallographic information about surfaces. (Full article...) - Image 7
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 8
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...) - Image 9
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 10
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...) - Image 11
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...) - Image 12
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...) - Image 13
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...) - Image 14
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 15
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...) - Image 16
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...) - Image 17
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 18
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 19
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...) - Image 20
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...) - Image 21
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, until its adverse effects on human health were more widely 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...) - Image 22
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...) - Image 23
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 24
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...) - Image 25
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...)
Selected mineralogist
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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...) - Image 2Karl Hugo Strunz (24 February 1910 – 19 April 2006) was a German mineralogist. He is best known for creating the Nickel-Strunz classification, the ninth edition of which was published together with Ernest Henry Nickel. (Full article...)
- Image 3Stanley Robert Mitchell (12 February 1881 – 22 March 1963) was an Australian commercial metallurgist as well as an amateur mineralogist and ethnologist. (Full article...)
- Image 4
Henri Longchambon (27 July 1896 in Clermont-Ferrand, Puy-de-Dôme – 20 March 1969 in Le Kremlin-Bicêtre) was a French politician and scientist. (Full article...) - Image 5Douglas Saxon Coombs CNZM (23 November 1924 – 23 December 2016) was a New Zealand mineralogist and petrologist. (Full article...)
- Image 6Sobolev, Vladimir Stepanovich (17 May 1908 in Lugansk – 1 September 1982 in Moscow) was a Russian geologist, working in mineralogy, petrology and theory of metamorphism. He was born in Lugansk, and died in Moscow. Sobolev predicted deposits of diamonds in Eastern Siberia. (Full article...)
- Image 7
Ours-Pierre-Armand Petit-Dufrénoy (5 September 1792 – 20 March 1857) was a French geologist and mineralogist. (Full article...) - Image 8Helen Dick Megaw (1 June 1907 – 26 February 2002) was an Irish crystallographer who was a pioneer in X-ray crystallography. She made measurements of the cell dimensions of ice and established the Perovskite crystal structure. (Full article...)
- Image 9
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 10John Sinkankas (May 15, 1915 – May 17, 2002) was a Navy officer and aviator, gemologist, gem carver and gem faceter, author of many books and articles on minerals and gemstones, and a bookseller and bibliographer of rare books. (Full article...)
- Image 11
Thomas Allan of Lauriston FRS FRSE FSA FLS (17 July 1777 – 12 September 1833) was a British mineralogist. (Full article...) - Image 12Friedrich Alfred Seifert (born 8 May 1941) is a German mineralogist and geophysicist. He is the founding director of Bayerisches Geoinstitut at University of Bayreuth. A silicate mineral, seifertite, is named after him. (Full article...)
- Image 13Joseph (Joe) Anthony Mandarino OC, FRSC (20 April 1929 in Chicago, Illinois – 19 September 2007) was an American-Canadian mineralogist and crystallographer. (Full article...)
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Ignaz Edler von Born, also known as Ignatius von Born (Hungarian: Born Ignác, Romanian: Ignațiu von Born, Czech: Ignác Born) (26 December 1742 in Alba Iulia, Grand Principality of Transylvania, Habsburg monarchy – 24 July 1791 in Vienna), was a mineralogist and metallurgist. He was a prominent freemason, being head of Vienna's lodge and an influential anti-clerical writer. He was the leading scientist in the Holy Roman Empire during the 1770s in the Age of Enlightenment.
His interests include mining, mineralogy, palaeontology, chemistry, metallurgy and malacology. (Full article...) - Image 15
Edward Daniel Clarke (5 June 1769 – 9 March 1822) was an English clergyman, naturalist, mineralogist, and traveller. (Full article...) - Image 16Naima Sahlbom (15 May 1871 – 29 March 1957) was a Swedish chemist, mineralogist, and peace activist. She is considered to be one of Sweden's most notable women chemists of the early 20th century. (Full article...)
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Marcel Alexandre Bertrand (2 July 1847 – 13 February 1907) was a French geologist born in Paris. He was the son of mathematician Joseph Louis François Bertrand (1822–1900), and son-in-law to physicist Éleuthère Mascart (1837-1908).
He studied at the École Polytechnique, and beginning in 1869 he attended the Ecole des Mines de Paris. From 1877 he carried out geological mapping studies of Provence, the Jura Mountains and the Alps. In 1886, he became an instructor at the École Nationale Supérieure des Mines, and in 1896 became a member of the Académie des sciences. (Full article...) - Image 18
Alexander Petrovich Karpinsky (Russian: Александр Петрович Карпинский, trl. Aljeksandr Pjetrovič Karpinskij; 7 January 1847 [O.S. 26 December 1846] – 15 July 1936) was a prominent Russian and Soviet geologist and mineralogist, and the president of the Russian Academy of Sciences, and later Academy of Sciences of the USSR, in 1917–1936. (Full article...) - Image 19Andrew Ketcham Barnett (1852–1914) was a mineral collector and dealer in Penzance, Cornwall, in the United Kingdom. He was Principal of the Penzance School of Mines (now part of the Camborne School of Mines), lectured on mining, and helped to build their mineral collection. He also served as Mayor of Penzance on seven occasions from 1906 to 1913.
Cooper writes of him:
:"Barnett was born in Chacewater, Cornwall in 1852. He was an original member of the Mineralogical Society, a Fellow of the Geological Society from 1875, and President of the Royal Geological Society of Cornwall 1907–08, having been awarded their Bolitho Medal in 1906. His classes on mineralogy in 1873 led to the establishment of the Mining and Science School at Penzance of which he became Principal. He was mayor of Penzance seven times from 1906 to 1913. Active as a mineral dealer from at least 1876 to 1887 at Chyandour, Penzance, he specialized in local specimens and occasionally sold minerals brought back from Australia by "Cousin Jack." In the 1881 Census he described himself as an assayer. He is the author of the now-rare Elementary Inorganic Chemistry; lecture notes, ca. 1900." (Full article...) - Image 20
Rodney Charles Ewing (born September 20, 1946) is an American mineralogist and materials scientist whose research is focused on the properties of nuclear materials.
He is the Frank Stanton Professor in Nuclear Security at the Center for International Security and Cooperation, a Senior Fellow of the Freeman Spogli Institute for International Studies, a Senior Fellow of the Precourt Institute for Energy, an Affiliate of the Stanford Woods Institute for the Environment, and a professor in the School of Earth, Energy and Environmental Sciences at Stanford University. (Full article...) - Image 21
Karl Georg von Raumer (9 April 1783 – 2 June 1865) was a German geologist and educator. (Full article...) - Image 22
James Reynolds Gregory (29 December 1832 – 15 December 1899) was a noted 19th-century British mineralogist. He founded a mineral specimen business in 1858 which is today known as Gregory, Bottley & Lloyd. Gregory's company had a reputation as one of the best in the business providing mineral samples for scientists as well as private collectors. He primarily bought his specimens at auction or from other collectors and dealers, rarely collecting from the field.
When he was sent in 1868 by diamond merchant Harry Emmanuel of London's Hatton Garden to Hopetown, South Africa, to determine if claims of diamonds being found there were true, he investigated and reported back, that "The whole story of the Cape diamond discoveries is false, and is simply one of the many schemes for trying to promote the employment and expenditure of capital in searching for this pereachous [sic] substance in the colony". (Full article...) - Image 23
Peter Woulfe (1727–1803) was an Anglo-Irish chemist and mineralogist. He first had the idea that wolframite might contain a previously undiscovered element (tungsten).
In 1771, Woulfe reported the formation of a yellow dye when indigo was treated with nitric acid. (Full article...) - Image 24Charles Louis Christ (March 12, 1916 – June 29, 1980) was an American scientist, geochemist and mineralogist. (Full article...)
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Pierre Louis Antoine Cordier (31 March 1777 – 30 March 1861) was a French geologist and mineralogist, and a founder of the French Geological Society. He was professor of geology at the Muséum national d'histoire naturelle in Paris from 1819 to 1861, and was responsible for the development of the geological gallery in the museum. (Full article...)
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General images
- Image 1Sphalerite crystal partially encased in calcite from the Devonian Milwaukee Formation of Wisconsin (from Mineral)
- Image 2Mohs Scale versus Absolute Hardness (from Mineral)
- Image 3Hübnerite, the manganese-rich end-member of the wolframite series, with minor quartz in the background (from Mineral)
- Image 4Red cinnabar (HgS), a mercury ore, on dolomite. (from Mineral)
- Image 5Black andradite, an end-member of the orthosilicate garnet group. (from Mineral)
- Image 7Native 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)
- Image 8Epidote often has a distinctive pistachio-green colour. (from Mineral)
- Image 9Mohs hardness kit, containing one specimen of each mineral on the ten-point hardness scale (from Mohs scale)
- Image 11An example of elbaite, a species of tourmaline, with distinctive colour banding. (from Mineral)
- Image 12When 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)
- Image 13Gypsum desert rose (from Mineral)
- Image 15Asbestiform tremolite, part of the amphibole group in the inosilicate subclass (from Mineral)
- Image 16Muscovite, a mineral species in the mica group, within the phyllosilicate subclass (from Mineral)
- Image 19Pink 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)
- Image 22Perfect basal cleavage as seen in biotite (black), and good cleavage seen in the matrix (pink orthoclase). (from Mineral)
- Image 23Diamond is the hardest natural material, and has a Mohs hardness of 10. (from Mineral)
- Image 24Schist 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)
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 when first noted, arsenoclasite appeared very similar to sarkinite (pictured), but with one perfect cleavage?
- ... that caryopilite was named for the Greek words for walnut and felt?
- ... that the mineral bobfergusonite has been found only in Canada and Argentina?
- ... that while the mineral magnesiopascoite was discovered in Utah, the two cotype specimens are in a museum in California?
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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Micas |
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Talcs |
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Pyrophyllite series |
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Kaolinites |
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Serpentines |
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Corrensites | |
Smectites and vermiculite family |
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Chlorites | |
Allophanes |
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Sepiolites |
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Pyrosmalites |
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Stilpnomelanes |
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Structural groups mainly; based on rruff.info/ima, modified |
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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