Portal:Minerals
Portal maintenance status: (May 2019)
|
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
-
Image 1
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 2
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 3
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 4
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...) -
Image 5
Chalcopyrite (/ˌkælkəˈpaɪˌraɪt, -koʊ-/ KAL-kə-PY-ryte, -koh-) is a copper iron sulfide mineral and the most abundant copper ore mineral. It has the chemical formula CuFeS2 and crystallizes in the tetragonal system. It has a brassy to golden yellow color and a hardness of 3.5 to 4 on the Mohs scale. Its streak is diagnostic as green-tinged black.
On exposure to air, chalcopyrite tarnishes to a variety of oxides, hydroxides, and sulfates. Associated copper minerals include the sulfides bornite (Cu5FeS4), chalcocite (Cu2S), covellite (CuS), digenite (Cu9S5); carbonates such as malachite and azurite, and rarely oxides such as cuprite (Cu2O). It is rarely found in association with native copper. Chalcopyrite is a conductor of electricity.
Copper can be extracted from chalcopyrite ore using various methods. The two predominant methods are pyrometallurgy and hydrometallurgy, the former being the most commercially viable. (Full article...) -
Image 6
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 7
Micas (/ˈmaɪkəz/ MY-kəz) are a group of silicate minerals whose outstanding physical characteristic is that individual mica crystals can easily be split into extremely thin elastic plates. This characteristic is described as perfect basal cleavage. Mica is common in igneous and metamorphic rock and is occasionally found as small flakes in sedimentary rock. It is particularly prominent in many granites, pegmatites, and schists, and "books" (large individual crystals) of mica several feet across have been found in some pegmatites.
Micas are used in products such as drywalls, paints, fillers, especially in parts for automobiles, roofing and shingles, as well as in electronics. The mineral is used in cosmetics and food to add "shimmer" or "frost." (Full article...) -
Image 8
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 9
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 10
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 11
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 12
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 13
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 14
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...) -
Image 15
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...) -
Image 16
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 17
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 18
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...) -
Image 19
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 20
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...) -
Image 21
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...) -
Image 22
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 23
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...) -
Image 24
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 25
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...)
Selected mineralogist
-
Image 1
Parker Cleaveland (January 1, 1780 – August 15, 1858) was an American geologist and mineralogist, born in Rowley, Massachusetts.
He was identified with the early progress of the natural sciences. After having attending the Dummer Academy in Byfield, Massachusetts, he graduated from Harvard in 1799, was tutor in mathematics there from 1803 to 1805, was chosen professor of mathematics and natural philosophy and lecturer on chemistry and mineralogy in Bowdoin College, a position which he retained until his death, although many professorships in other colleges and the presidency of his own were offered to him. He was elected an Associate Fellow of the American Academy of Arts and Sciences in 1809 and to the American Philosophical Society in 1818. (Full article...) -
Image 2Carl Schulz (12 November 1851 – 15 August 1944) was a Norwegian educator and politician for the Liberal Party. He became known as a teacher of physics, electrotechnics and mineralogy before advancing to being school director. (Full article...)
-
Image 3
Gaius Plinius Secundus (AD 23/24 – AD 79), called Pliny the Elder (/ˈplɪni/), was a Roman author, naturalist, natural philosopher, naval and army commander of the early Roman Empire, and a friend of the emperor Vespasian. He wrote the encyclopedic Naturalis Historia (Natural History), which became an editorial model for encyclopedias. He spent most of his spare time studying, writing, and investigating natural and geographic phenomena in the field.
Among Pliny's greatest works was the twenty-volume Bella Germaniae ("The History of the German Wars"), which is no longer extant. Bella Germaniae, which began where Aufidius Bassus' Libri Belli Germanici ("The War with the Germans") left off, was used as a source by other prominent Roman historians, including Plutarch, Tacitus, and Suetonius. Tacitus may have used Bella Germaniae as the primary source for his work, De origine et situ Germanorum ("On the Origin and Situation of the Germans"). (Full article...) -
Image 4
Franz Ernst Brückmann (27 September 1697 – 21 March 1753) was a German mineralogist born at Marienthal near Helmstedt. Having qualified as a physician in 1721, he practised at Braunschweig and afterwards at Wolfenbüttel (from 1728). In 1747 he was appointed medical assessor in Braunschweig.
His leisure time was given up to natural history, and especially to mineralogy and botany. He appears to have been the first to introduce the term "oolithus" to rocks that resemble in structure the roe of a fish; whence the terms "oolite" and "oolitic". He died at Wolfenbüttel. (Full article...) -
Image 5
Johan Afzelius (13 June 1753 in Larv – 20 May 1837 in Uppsala) was a Swedish chemist and notable as the doctoral advisor of one of the founders of modern chemistry, Jöns Jacob Berzelius. He was the brother of botanist Adam Afzelius and physician Pehr von Afzelius.
Afzelius received his PhD at Uppsala University in 1776 under Torbern Olof Bergman. In 1780 he became a lecturer at Uppsala and in 1784 a professor of chemistry. From 1792 to 1797 he undertook research trips to Norway, Denmark and Russia in order to study mineral deposits and to visit scientific institutions. His remarkable mineral collection became part of Uppsala University's mineral cabinet. (Full article...) -
Image 6Johann Karl Wilhelm Voigt (20 February 1752 in Allstedt – 2 January 1821 in Ilmenau) was a German mineralogist and mining engineer.
He initially studied law at the University of Jena, then in 1776 enrolled at the Mining Academy in Freiberg as a pupil of Abraham Gottlob Werner. He later relocated to Weimar, where in 1783 he was named secretary of the Bergwerkskommission (mining commission). During his time spent in Weimar he developed a close friendship with Johann Wolfgang von Goethe — through Voigt, Goethe received an education in mineralogy. From 1789 to 1821, he served as Bergrath (councillor of mines) in Ilmenau. (Full article...) -
Image 7
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 8Pierre Bernard Palassou (9 June 1745, Oloron-Sainte-Marie – 9 April 1830, Ogenne-Camptort) was a French naturalist known for pioneer geological and mineralogical studies of the Pyrénées.
He was a correspondent member of the Académie des sciences (1816–1830) and an honorary member of the Société linnéenne de Paris (1821). His name is associated with the "Poudingues de Palassou", which are enormous beds of conglomerate rock found in the Pyrénées. In 1784 he described Quercus palensis (Pyrenean oak) of the botanical family Fagaceae, (synonym Quercus pyrenaica Willd.). (Full article...) -
Image 9
Thomas Egleston (December 9, 1832 – January 15, 1900) was an American engineer who helped found Columbia University's School of Mines, now the Fu Foundation School of Engineering and Applied Science. Throughout his lifetime, Egleston published numerous lectures and books on metallurgy. Many of his books are preserved today at the archive in the Library of Congress. (Full article...) -
Image 10
Nils Adolf Erik Nordenskiöld (18 November 1832 – 12 August 1901) was a Finland-Swedish aristocrat, geologist, mineralogist and Arctic explorer. He was a member of the Fenno-Swedish Nordenskiöld family of scientists and held the title of a friherre (baron). His ethnicity was Finnish-Swedish.
Born in the Grand Duchy of Finland at the time it was a part of the Russian Empire, he was later, due to his political activity, forced to move to Sweden, where he later became a member of the Parliament of Sweden and of the Swedish Academy. He led the Vega Expedition along the northern coast of Eurasia in 1878–1879. This was the first complete crossing of the Northeast Passage. Initially a troubled enterprise, the successful expedition is considered to be among the highest achievements in the history of Swedish science. (Full article...) -
Image 11Arthur Francis "Bud" Buddington (November 29, 1890 – December 25, 1980) was an American geologist. Born in Wilmington, Delaware, he grew up there and in West Mystic, Connecticut. He was educated at Brown University and Princeton University.
After short stints teaching at Brown and Princeton, serving in the Chemical Warfare Service during World War I, and researching at the Carnegie Institution for Science, Buddington settled at Princeton, where he taught for nearly 40 years. He chaired the Department of Geology from 1936 to 1950. He also had a long career with the U.S. Geological Survey (USGS), doing field work for that agency in Alaska, Oregon, and the northeastern United States. (Full article...) -
Image 12
Karl Rössler (6 May 1788, in Wiesbaden – 23 August 1863, in Hanau) was a German manufacturer and mineralogist.
After a business apprenticeship in Frankfurt am Main, he acquired in 1818 a hat factory, which he transformed into a highly successful company. He had a keen interest in the geology, mineralogy and paleontology of the Wetterau, and accordingly, collected numerous minerals and fossils of the region. During his career, he worked closely with geologist Leopold von Buch. (Full article...) -
Image 13
Harry von Eckermann (1886–1969) was a Swedish industrialist, mineralogist and geologist. His studies were centered around anorogenic alkaline igneous rocks occurring in the Baltic Shield. Following this line he studied the Alnö Complex, Norra Kärr Alkaline Complex and various Rapakivi granites.
In a 1948 publication on Alnö, von Eckermann correctly claimed a magmatic origin of carbonatite, albeit his finds were only widely accepted after the Ol Doinyo Lengai eruption of carbonatite lava in the 1960s showed contemporary evidence on the existence of such magmas. In relation to the mid-20th century granitization controversy von Eckermann rejected the notion that rapakivi granites were Jotnian sediments turned into granite. (Full article...) -
Image 14
Luiz Alberto Dias Menezes (5 October 1950 – 9 July 2014) was a geologist, mineralogist and mineral dealer from Brazil. He was born in São Paulo.
He collected the material that was used for the discovery of new mineral was named in his honor as menezesite. He also contributed extensively in mineralogy of Brazil, participating in the discovery of up to seven mineral species. (Full article...) -
Image 15Douglas Saxon Coombs CNZM (23 November 1924 – 23 December 2016) was a New Zealand mineralogist and petrologist. (Full article...)
-
Image 16Georg Heinrich Otto Volger (30 January 1822 – 18 October 1897) was a German geologist from Lüneburg. He was the founder and first chairman of the Freies Deutsches Hochstift, which he led from 1859 to 1882. (Full article...)
-
Image 17Charles-Victor Mauguin (French: [ʃaʁl.vik.tɔʁ mo.gɛ̃]; 19 September 1878 – 25 April 1958), more often Charles Mauguin, was a French mineralogist and crystallographer. He and Carl Hermann invented an international standard notation for crystallographic groups called Hermann–Mauguin notation (also sometimes called international notation). (Full article...)
-
Image 18Anselmus 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 19
Sten Anders Hjalmar Sjögren (13 June 1856, Färnebo, Värmland – 23 March 1922, Stockholm) was a Swedish geologist and mineralogist. (Full article...) -
Image 20
Christian Ernst Weiss (12 May 1833, in Eilenburg – 4 July 1890, in Schkeuditz) was a German mineralogist, geologist and palaeontologist.
He is not to be confused with the historian Christian Ernst Weiße (1766–1832). (Full article...) -
Image 21William Sefton Fyfe, CC FRSC FRS FRSNZ (4 June 1927 – 11 November 2013) was a New Zealand geologist and Professor Emeritus in the department of Earth Sciences at the University of Western Ontario. He is widely considered among the world's most eminent geochemists. (Full article...)
-
Image 22
Torbern Olaf (Olof) Bergman (KVO) (20 March 1735 – 8 July 1784) was a Swedish chemist and mineralogist noted for his 1775 Dissertation on Elective Attractions, containing the largest chemical affinity tables ever published. Bergman was the first chemist to use the A, B, C, etc., system of notation for chemical species. (Full article...) -
Image 23
Arthur Hutchinson OBE FRS (6 July 1866 – 12 December 1937) was a British mineralogist. During World War I, and at the request of the Admiralty, he was asked to design gas masks suitable for the Navy; for his work, he was awarded the OBE. Hutchinson was elected a Fellow of the Royal Society in 1922. He was master of Pembroke College, Cambridge, from 1928 to 1937, served on the Council of the Royal Society from 1932 to 1934, and was the Society's Vice-President for the year 1933-34. (Full article...) -
Image 24
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 25Lewis Caleb Beck (4 October 1798 Schenectady – 20 April 1853 Albany, New York) was an American physician, botanist, chemist, and mineralogist. The standard author abbreviation L.C.Beck is used to indicate this person as the author when citing a botanical name.[1] (Full article...)
Related portals
Get involved
For editor resources and to collaborate with other editors on improving Wikipedia's Minerals-related articles, see WikiProject Rocks and minerals.
General images
-
Image 4An example of elbaite, a species of tourmaline, with distinctive colour banding. (from Mineral)
-
Image 5Pink cubic halite (NaCl; halide class) crystals on a nahcolite matrix (NaHCO3; a carbonate, and mineral form of sodium bicarbonate, used as baking soda). (from Mineral)
-
Image 8Schist 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)
-
Image 10Mohs Scale versus Absolute Hardness (from Mineral)
-
Image 11Epidote often has a distinctive pistachio-green colour. (from Mineral)
-
Image 12Mohs hardness kit, containing one specimen of each mineral on the ten-point hardness scale (from Mohs scale)
-
Image 13Native gold. Rare specimen of stout crystals growing off of a central stalk, size 3.7 x 1.1 x 0.4 cm, from Venezuela. (from Mineral)
-
Image 14Diamond is the hardest natural material, and has a Mohs hardness of 10. (from Mineral)
-
Image 17Gypsum desert rose (from Mineral)
-
Image 18Black andradite, an end-member of the orthosilicate garnet group. (from Mineral)
-
Image 19Red cinnabar (HgS), a mercury ore, on dolomite. (from Mineral)
-
Image 20Sphalerite crystal partially encased in calcite from the Devonian Milwaukee Formation of Wisconsin (from Mineral)
-
Image 21Asbestiform tremolite, part of the amphibole group in the inosilicate subclass (from Mineral)
-
Image 22When 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 23Perfect basal cleavage as seen in biotite (black), and good cleavage seen in the matrix (pink orthoclase). (from Mineral)
-
Image 24Muscovite, a mineral species in the mica group, within the phyllosilicate subclass (from Mineral)
-
Image 25Hübnerite, the manganese-rich end-member of the wolframite series, with minor quartz in the background (from Mineral)
In the news
- 3 May 2024 –
- Panama bans First Quantum Minerals from extracting copper following the closure of its Cobre Panamá mine last year. (Reuters) (The Globe and Mail)
Did you know ...?
- ... that the mineral diaboleite (pictured) was so named out of desperation?
- ... that silicate perovskites may make up to 93% of the lower mantle and that the magnesium form is considered to be Earth's most abundant mineral?
- ... that while huemulite was discovered in 1959, it was not described until 1966?
Subcategories
- Select [►] to view subcategories
Topics
Overview | ||
---|---|---|
Common minerals |
Ore minerals, mineral mixtures and ore deposits | |||||||||
---|---|---|---|---|---|---|---|---|---|
Ores |
| ||||||||
Deposit types |
Borates | |||||
---|---|---|---|---|---|
Carbonates | |||||
Oxides |
| ||||
Phosphates | |||||
Silicates | |||||
Sulfides | |||||
Other |
|
Crystalline | |||||||
---|---|---|---|---|---|---|---|
Cryptocrystalline | |||||||
Amorphous | |||||||
Miscellaneous | |||||||
Notable varieties |
|
Oxide minerals |
| ||||
---|---|---|---|---|---|
Silicate minerals | |||||
Other |
Gemmological classifications by E. Ya. Kievlenko (1980), updated | |||||||||
Jewelry stones |
| ||||||||
Jewelry-Industrial stones |
| ||||||||
Industrial stones |
| ||||||||
Mineral identification | |
---|---|
"Special cases" ("native elements and organic minerals") |
|
---|---|
"Sulfides and oxides" |
|
"Evaporites and similars" |
|
"Mineral structures with tetrahedral units" (sulfate anion, phosphate anion, silicon, etc.) |
|
Associated Wikimedia
The following Wikimedia Foundation sister projects provide more on this subject:
-
Commons
Free media repository -
Wikibooks
Free textbooks and manuals -
Wikidata
Free knowledge base -
Wikinews
Free-content news -
Wikiquote
Collection of quotations -
Wikisource
Free-content library -
Wikiversity
Free learning tools -
Wiktionary
Dictionary and thesaurus
References
- Pages with French IPA
- Manually maintained portal pages from May 2019
- All manually maintained portal pages
- Portals with triaged subpages from May 2019
- All portals with triaged subpages
- Portals with named maintainer
- Automated article-slideshow portals with 31–40 articles in article list
- Automated article-slideshow portals with 201–500 articles in article list
- Portals needing placement of incoming links