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. Diamond as a form of carbon is tasteless, odourless, strong, brittle solid, colourless in pure form, a poor conductor of electricity, and insoluble in water. 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). Natural and synthetic diamonds are most commonly distinguished using optical techniques or thermal conductivity measurements. (Full article...) -
Image 2Quartz crystal cluster from Brazil
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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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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A crystalline solid: atomic resolution image of strontium titanate. Brighter spots are columns of strontium atoms and darker ones are titanium-oxygen columns.
Crystallography is the branch of science devoted to the study of molecular and crystalline structure and properties. 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 2014 the International Year of Crystallography.
Crystallography is a broad topic, and many of its subareas, such as X-ray crystallography, are themselves important scientific topics. Crystallography ranges from the fundamentals of crystal structure to the mathematics of crystal geometry, including those that are not periodic or quasicrystals. At the atomic scale it can involve the use of X-ray diffraction to produce experimental data that the tools of X-ray crystallography can convert into detailed positions of atoms, and sometimes electron density. At larger scales it includes experimental tools such as orientational imaging to examine the relative orientations at the grain boundary in materials. Crystallography plays a key role in many areas of biology, chemistry, and physics, as well new developments in these fields. (Full article...) -
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Turquoise is an opaque, blue-to-green mineral that is a hydrous phosphate of copper and aluminium, with the chemical formula CuAl6(PO4)4(OH)8·4H2O. It is rare and valuable in finer grades and has been prized as a gemstone for millennia due to its hue.
Like most other opaque gems, turquoise has been devalued by the introduction of treatments, imitations, and synthetics into the market. The robin egg blue or sky blue color of the Persian turquoise mined near the modern city of Nishapur, Iran, has been used as a guiding reference for evaluating turquoise quality. (Full article...) -
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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 US $4.24 billion. (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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Asbestos (/æsˈbɛstəs, æz-, -tɒs/ ass-BES-təs, az-, -toss) is a group of naturally occurring, toxic, carcinogenic and fibrous silicate minerals. 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 around 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, around 255,000 people are thought to die each year from diseases related to asbestos exposure. 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 until 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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Mineralogy applies principles of chemistry, geology, physics and materials science to the study of minerals
Mineralogy is a subject of geology specializing in the scientific study of the chemistry, crystal structure, and physical (including optical) properties of minerals and mineralized artifacts. Specific studies within mineralogy include the processes of mineral origin and formation, classification of minerals, their geographical distribution, as well as their utilization. (Full article...) -
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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 11Dolomite (white) on talc
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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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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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. In Roman times, cinnabar was highly valued as paint for walls, especially interiors, since it darkened when used outdoors due to exposure to sunlight.
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...) -
Image 14Amethyst cluster from Artigas, Uruguay
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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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 the amorphous (chemical) physical structure, it is classified as a mineraloid, unlike crystalline forms of silica, which are considered minerals. It is deposited at a relatively low temperature and may occur in the fissures of almost any kind of rock, being most commonly found with limonite, sandstone, rhyolite, marl, and basalt.
The name opal is believed to be derived from the Sanskrit word upala (उपल), which means 'jewel', and later the Greek derivative opállios (ὀπάλλιος).
There are two broad classes of opal: precious and common. Precious opal displays play-of-color (iridescence); common opal does not. Play-of-color is defined as "a pseudo chromatic optical effect resulting in flashes of colored light from certain minerals, as they are turned in white light." The internal structure of precious opal causes it to diffract light, resulting in play-of-color. Depending on the conditions in which it formed, opal may be transparent, translucent, or opaque, and the background color may be white, black, or nearly any color of the visual spectrum. Black opal is considered the rarest, while white, gray, and green opals are the most common. (Full article...) -
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Garnets ( /ˈɡɑːrnɪt/) are a group of silicate minerals that have been used since the Bronze Age as gemstones and abrasives.
Garnet minerals, while sharing similar physical and crystallographic properties, exhibit a wide range of chemical compositions, defining distinct species. These species fall into two primary solid solution series: the pyralspite series (pyrope, almandine, spessartine), with the general formula [Mg,Fe,Mn]3Al2(SiO4)3; and the ugrandite series (uvarovite, grossular, andradite), with the general formula Ca3[Cr,Al,Fe]2(SiO4)3. Notable varieties of grossular include hessonite and tsavorite. (Full article...) -
Image 17A lustrous crystal of zircon perched on a tan matrix of calcite from the Gilgit District of Pakistan
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...) -
Image 18Halite from the Wieliczka salt mine, Małopolskie, Poland
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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Micas (/ˈmaɪkəz/ MY-kəz) are a group of silicate minerals whose outstanding physical characteristic is that individual mica crystals can easily be split into fragile 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, and fillers, especially in parts for automobiles, roofing, and in electronics. The mineral is used in cosmetics and food to add "shimmer" or "frost". (Full article...) -
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Beryl (/ˈbɛrəl/ BERR-əl) is a mineral composed of beryllium aluminium silicate with the chemical formula Be3Al2(SiO3)6. 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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Graphite (/ˈɡræfaɪt/) is a crystalline allotrope (form) of the element carbon. It consists of many stacked layers of graphene, typically in excess of hundreds of layers. 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 many critical industries including refractories (50%), lithium-ion batteries (18%), foundries (10%), and lubricants (5%), among others (17%). Graphite converts to diamond under extremely high pressure and temperature. Graphite's low cost, thermal and chemical inertness and characteristic conductivity of heat and electricity finds numerous applications in high energy and high temperature processes. (Full article...) -
Image 22Deep green isolated fluorite crystal resembling a truncated octahedron, set upon a micaceous matrix, from Erongo Mountain, Erongo Region, Namibia (overall size: 50 mm × 27 mm, crystal size: 19 mm wide, 30 g)
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 glasses, so fluorite is useful in making apochromatic lenses, and particularly valuable 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. (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 24Galena with minor pyrite
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.
As a pure specimen held in the hand, under standard temperature and pressure, galena is insoluble in water and so is almost non-toxic. Handling galena under these specific conditions (such as in a museum or as part of geology instruction) poses practically no risk; however, as lead(II) sulfide is reasonably reactive in a variety of environments, it can be highly toxic if swallowed or inhaled, particularly under prolonged or repeated exposure. (Full article...) -
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Corundum is a crystalline form of aluminium oxide (Al2O3) typically containing traces of iron, titanium, vanadium, and chromium. It is a rock-forming mineral. It is a naturally transparent material, but can have different colors depending on the presence of transition metal impurities in its crystalline structure. Corundum has two primary gem varieties: ruby and sapphire. Rubies are red due to the presence of chromium, and sapphires exhibit a range of colors depending on what transition metal is present. A rare type of sapphire, padparadscha sapphire, is pink-orange.
The name "corundum" is derived from the Tamil-Dravidian word kurundam (ruby-sapphire) (appearing in Sanskrit as kuruvinda).
Because of corundum's hardness (pure corundum is defined to have 9.0 on the Mohs scale), it can scratch almost all other minerals. Emery, a variety of corundum with no value as a gemstone, is commonly used as an abrasive on sandpaper and on large tools used in machining metals, plastics, and wood. 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...)
Selected mineralogist
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Image 1William Alexander (Alex) Deer FRS (26 October 1910 – 8 February 2009) was a distinguished British geologist, petrologist and mineralogist. (Full article...)
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Image 2Martin Julian Buerger (April 8, 1903 – February 26, 1986) was an American crystallographer. He was a Professor of Mineralogy at the Massachusetts Institute of Technology. He invented the X-ray precession camera for studies in crystallography. Buerger authored twelve textbooks/monographs and over 200 technical articles. He was awarded the Arthur L. Day Medal by the Geological Society of America in 1951. The mineral fluor-buergerite was named for him. The MJ Buerger Award (established by the American Crystallographic Association) was established in his honor.
Buerger was a member of the Provisional International Crystallographic Committee chaired by P. P. Ewald from 1946 to 1948, and he continued as a member of the IUCr Executive Committee from 1948 to 1951. He was also a member of the Commission on International Tables from its establishment in 1948 until 1981. (Full article...) -
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Sir William Lawrence Bragg (31 March 1890 – 1 July 1971) was an Australian-born British physicist who shared the 1915 Nobel Prize in Physics with his father William Henry Bragg "for their services in the analysis of crystal structure by means of X-rays", an important step in the development of X-ray crystallography.
As of 2024, he is the youngest ever Nobel laureate in physics, or in any science category, having received the award at the age of 25. Bragg was the director of the Cavendish Laboratory, Cambridge, when the discovery of the structure of DNA was reported by James D. Watson and Francis Crick in February 1953. (Full article...) -
Image 4Maynard Bixby (June 28, 1853 – February 18, 1935) was an American mineralogist and mineral collector. (Full article...)
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James Nicol
James Nicol FRSE FGS (12 August 1810 – 8 April 1879) was a Scottish geologist. (Full article...) -
Image 6Bertram Eugene Warren (June 28, 1902 – June 27, 1991) was an American crystallographer. His studies of X-rays provided much knowledge and understanding of both crystalline and non-crystalline materials. He also worked on changing amorphous solids to a crystalline state. (Full article...)
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Arthur Aikin (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...) -
Image 8Carlo 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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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...) -
Image 10Gold and Diamonds - from John Mawe's 1812 book Travels in the Interior of Brazil
illustrated by James Sowerby
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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Auguste Bravais (French pronunciation: [oɡyst bʁavɛ]; 23 August 1811, Annonay, Ardèche – 30 March 1863, Le Chesnay, France) was a French physicist known for his work in crystallography, the conception of Bravais lattices, and the formulation of Bravais law. Bravais also studied magnetism, the northern lights, meteorology, geobotany, phyllotaxis, astronomy, statistics and hydrography.
He studied at the Collège Stanislas in Paris before joining the École Polytechnique in 1829, where he was a classmate of groundbreaking mathematician Évariste Galois, whom Bravais actually beat in a scholastic mathematics competition. Towards the end of his studies he became a naval officer, and sailed on the Finistere in 1832 as well as the Loiret afterwards. He took part in hydrographic work along the Algerian Coast. He participated in the Recherche expedition and helped the Lilloise in Spitzbergen and Lapland. (Full article...) -
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Antonio D'Achiardi (28 November 1839, in Pisa – 10 December 1902, in Pisa) was an Italian geologist, paleontologist and mineralogist known for his mineralogical and paleontological studies of Tuscany. He was the father of the mineralogist Giovanni D'Achiardi [it], and the artist, Pietro D'Achiardi.
In 1859 he received his doctorate in sciences from the University of Pisa, afterwards working as an assistant for chemistry (from 1861). Three months after this appointment, he lost the use of his left eye due to a laboratory accident involving nitric acid. He subsequently abandoned his career in chemistry, and instead devoted his attention to geology and mineralogy, becoming a student of Giuseppe Meneghini. He later became a professor of geology at Pavia and in 1874 was appointed a professor of mineralogy at the University of Pisa. In 1881 he established a laboratory of mineralogy at Pisa. (Full article...) -
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Robert Miller Hazen (born November 1, 1948) is an American mineralogist and astrobiologist. He is a research scientist at the Carnegie Institution of Washington's Geophysical Laboratory and Clarence Robinson Professor of Earth Science at George Mason University, in the United States. Hazen is the Executive Director of the Deep Carbon Observatory. (Full article...) -
Image 14Archibald Bruce (February 1777 – February 22, 1818) was an American physician and mineralogist. (Full article...)
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Franz Ludwig von Cancrin
Franz Ludwig von Cancrin (February 21, 1738 in Breidenbach – 1812) was a German mineralogist, metallurgist, architect and writer.
He was born into a German mining family where he was trained by his father in the science of mining. In 1764, he entered the service of the landgrave of Hesse-Kassel at Hanau, becoming professor of mathematics at the military academy, head of the civil engineering department of the state, director of the theatre and (1774) of the mint. A work on the copper mines of Elesse (1767) earned him a European reputation, and in 1783 he accepted from Catherine II of Russia the directorship of the famous Staraya salt-works, living thenceforth in Russia. (Full article...) -
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Friedrich Johann Karl Becke (31 December 1855, in Prague – 18 June 1931, in Vienna) was an Austrian mineralogist and petrographer. (Full article...) -
Image 17Justus Ludwig Adolf Roth (September 15, 1818, Hamburg – April 1, 1892) was a German geologist and mineralogist. (Full article...)
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Image 18Ralph Early Grim (February 25, 1902 – August 19, 1989) was an American geologist and scientist, often referred to as the "Father of Mineralogy" because he made many discoveries during his investigations of clay materials. He was one of the most outstanding mineralogists of his time and was well-known throughout the world in the field of clay science and technology. Grim's career spanned over 60 years and he received many honors and awards in the field of mineralogy. Some of the textbooks he wrote have been standard university textbooks in mineralogy for many years. (Full article...)
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Alexander von Schrenk
Alexander Gustav von Schrenk (4 February 1816 – 25 June 1876) was a Baltic German-Russian naturalist born near Tula in what was then the Russian Empire. He was a brother to zoologist Leopold von Schrenck (1826–1894).
From 1834 to 1837, he studied sciences at the University of Dorpat (Tartu), later spending several years as an assistant at the botanical garden in St. Petersburg. He was habilitated for mineralogy at Dorpat, where from 1849 he served as a lecturer. From 1858 he spent the next ten years at his wife's manor in Pühajärve (Heiligensee), Livonia, returning to Dorpat in 1868, where he died several years later. (Full article...) -
Image 20Bust of Shen at the Beijing Ancient Observatory
Shen Kuo (Chinese: 沈括; 1031–1095) or Shen Gua, courtesy name Cunzhong (存中) and pseudonym Mengqi (now usually given as Mengxi) Weng (夢溪翁), was a Chinese polymath, scientist, and statesman of the Song dynasty (960–1279). Shen was a master in many fields of study including mathematics, optics, and horology. In his career as a civil servant, he became a finance minister, governmental state inspector, head official for the Bureau of Astronomy in the Song court, Assistant Minister of Imperial Hospitality, and also served as an academic chancellor. At court his political allegiance was to the Reformist faction known as the New Policies Group, headed by Chancellor Wang Anshi (1021–1085).
In his Dream Pool Essays or Dream Torrent Essays (夢溪筆談; Mengxi Bitan) of 1088, Shen was the first to describe the magnetic needle compass, which would be used for navigation (first described in Europe by Alexander Neckam in 1187). Shen discovered the concept of true north in terms of magnetic declination towards the north pole, with experimentation of suspended magnetic needles and "the improved meridian determined by Shen's [astronomical] measurement of the distance between the pole star and true north". This was the decisive step in human history to make compasses more useful for navigation, and may have been a concept unknown in Europe for another four hundred years (evidence of German sundials made circa 1450 show markings similar to Chinese geomancers' compasses in regard to declination). (Full article...) -
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Gustav Anton Zeuner (30 November 1828 – 17 October 1907) was a German physicist, engineer and epistemologist, considered the founder of technical thermodynamics and of the Dresden School of Thermodynamics. (Full article...) -
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Karl Friedrich August Rammelsberg (1 April 1813 – 28 December 1899) was a German mineralogist from Berlin, Prussia. (Full article...) -
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André Laugier (1770–1832)
André Laugier (1 August 1770, in Lisieux – 19 April 1832, in Paris) was a French chemist, pharmacist and mineralogist. He was a cousin to famed chemist Antoine François Fourcroy and the father of astronomer Paul Auguste Ernest Laugier (1812–1872).
He received his education in his hometown of Lisieux, and during the French Revolution, was tasked with collecting church bells in Bretagne in order for them to be melted down for the production of cannons. In 1794 he was employed as head of the gunpowder and saltpeter works at the Comite de salut public. In 1797 he received his master's degree in pharmacy, and subsequently taught classes in chemistry and pharmacy at the military training schools in Toulon and Lille. (Full article...) -
Image 24Hendrik 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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Lettsom caricatured as the diplomat 'Tapeworm' (centre, standing): pencil sketch by William Makepeace Thackeray
William Garrow Lettsom FRAS (1805 – 14 December 1887) was a British diplomat and scientist. He was instrumental in revealing the text of the secret Treaty of the Triple Alliance between Argentina, the Empire of Brazil and Uruguay. (Full article...)
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Did you know...
- ... that nine days after his heart transplant, J. C. Walter Jr. merged his company Houston Oil & Minerals with Tenneco, then retired to his ranch and shortly after founded Walter Oil & Gas?
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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 1Mohs Scale versus Absolute Hardness (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 5Perfect basal cleavage as seen in biotite (black), and good cleavage seen in the matrix (pink orthoclase). (from Mineral)
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Image 6When 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 8An example of elbaite, a species of tourmaline, with distinctive colour banding. (from Mineral)
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Image 10Hübnerite, the manganese-rich end-member of the wolframite series, with minor quartz in the background (from Mineral)
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Image 12Gypsum desert rose (from Mineral)
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Image 13Black andradite, an end-member of the orthosilicate garnet group. (from Mineral)
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Image 14Sphalerite crystal partially encased in calcite from the Devonian Milwaukee Formation of Wisconsin (from Mineral)
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Image 15Epidote often has a distinctive pistachio-green colour. (from Mineral)
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Image 16Diamond is the hardest natural material, and has a Mohs hardness of 10. (from Mineral)
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Image 18Schist 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 19Red cinnabar (HgS), a mercury ore, on dolomite. (from Mineral)
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Image 21Asbestiform tremolite, part of the amphibole group in the inosilicate subclass (from Mineral)
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Image 23Mohs hardness kit, containing one specimen of each mineral on the ten-point hardness scale (from Mohs scale)
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Image 24Native 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 26Muscovite, a mineral species in the mica group, within the phyllosilicate subclass (from Mineral)
Did you know ...?
- ... that while bultfonteinite (pictured) was discovered as early as 1903, the mineral wasn't described until 1932?
- ... that the minerals armalcolite, pyroxferroite and tranquillityite were discovered in lunar rocks?
- ... that taaffeite, one of the world's rarest gemstones, is the first mineral known to contain both beryllium and magnesium as essential components?
- ... that the newly discovered mineral krotite likely was one of the earliest minerals formed in the Solar System?
Subcategories
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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