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
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 2
Chalcopyrite (/ˌkælkəˈpaɪˌraɪt, -koʊ-/ KAL-kə-PY-ryte, -koh-) is a copper iron sulfide mineral and the most abundant copper ore mineral. It has the chemical formula CuFeS2 and crystallizes in the tetragonal system. It has a brassy to golden yellow color and a hardness of 3.5 to 4 on the Mohs scale. Its streak is diagnostic as green-tinged black.
On exposure to air, chalcopyrite tarnishes to a variety of oxides, hydroxides, and sulfates. Associated copper minerals include the sulfides bornite (Cu5FeS4), chalcocite (Cu2S), covellite (CuS), digenite (Cu9S5); carbonates such as malachite and azurite, and rarely oxides such as cuprite (Cu2O). It is rarely found in association with native copper. Chalcopyrite is a conductor of electricity.
Copper can be extracted from chalcopyrite ore using various methods. The two predominant methods are pyrometallurgy and hydrometallurgy, the former being the most commercially viable. (Full article...) -
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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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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 5
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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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...) -
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Dolomite (/ˈdɒl.əˌmaɪt, ˈdoʊ.lə-/) is an anhydrous carbonate mineral composed of calcium magnesium carbonate, ideally CaMg(CO3)2. The term is also used for a sedimentary carbonate rock composed mostly of the mineral dolomite (see Dolomite (rock)). An alternative name sometimes used for the dolomitic rock type is dolostone. (Full article...) -
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Beryl (/ˈbɛrəl/ BERR-əl) is a mineral composed of beryllium aluminium silicate with the chemical formula Be3Al2Si6O18. Well-known varieties of beryl include emerald and aquamarine. Naturally occurring hexagonal crystals of beryl can be up to several meters in size, but terminated crystals are relatively rare. Pure beryl is colorless, but it is frequently tinted by impurities; possible colors are green, blue, yellow, pink, and red (the rarest). It is an ore source of beryllium. (Full article...) -
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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 10
Turquoise is an opaque, blue-to-green mineral that is a hydrous phosphate of copper and aluminium, with the chemical formula CuAl6(PO4)4(OH)8·4H2O. It is rare and valuable in finer grades and has been prized as a gemstone for millennia due to its hue.
Like most other opaque gems, turquoise has been devalued by the introduction of treatments, imitations, and synthetics into the market. The robin egg blue or sky blue color of the Persian turquoise mined near the modern city of Nishapur, Iran, has been used as a guiding reference for evaluating turquoise quality. (Full article...) -
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In crystallography, 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...) -
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In crystallography, the cubic (or isometric) crystal system is a crystal system where the unit cell is in the shape of a cube. This is one of the most common and simplest shapes found in crystals and minerals.
There are three main varieties of these crystals:- Primitive cubic (abbreviated cP and alternatively called simple cubic)
- Body-centered cubic (abbreviated cI or bcc)
- Face-centered cubic (abbreviated cF or fcc)
Note: the term fcc is often used in synonym for the cubic close-packed or ccp structure occurring in metals. However, fcc stands for a face-centered-cubic Bravais lattice, which is not necessarily close-packed when a motif is set onto the lattice points. E.g. the diamond and the zincblende lattices are fcc but not close-packed.
Each is subdivided into other variants listed below. Although the unit cells in these crystals are conventionally taken to be cubes, the primitive unit cells often are not. (Full article...) -
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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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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...) -
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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...) -
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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...) -
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Zeolite is a family of several microporous, crystalline aluminosilicate materials commonly used as commercial adsorbents and catalysts. They mainly consist of silicon, aluminium, oxygen, and have the general formula Mn+
1/n(AlO
2)−
(SiO
2)
x・yH
2O where Mn+
1/n is either a metal ion or H+. These positive ions can be exchanged for others in a contacting electrolyte solution. H+
exchanged zeolites are particularly useful as solid acid catalysts.
The term was originally coined in 1756 by Swedish mineralogist Axel Fredrik Cronstedt, who observed that rapidly heating a material, believed to have been stilbite, produced large amounts of steam from water that had been adsorbed by the material. Based on this, he called the material zeolite, from the Greek ζέω (zéō), meaning "to boil" and λίθος (líthos), meaning "stone".
Zeolites occur naturally, but are also produced industrially on a large scale. , 253 unique zeolite frameworks have been identified, and over 40 naturally occurring zeolite frameworks are known. Every new zeolite structure that is obtained is examined by the International Zeolite Association Structure Commission (IZA-SC) and receives a three-letter designation. (Full article...) -
Image 18
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...) -
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Cinnabar (/ˈsɪnəˌbɑːr/; from Ancient Greek κιννάβαρι (kinnábari)), or cinnabarite (/ˌsɪnəˈbɑːraɪt/), also known as mercurblende is the bright scarlet to brick-red form of mercury(II) sulfide (HgS). It is the most common source ore for refining elemental mercury and is the historic source for the brilliant red or scarlet pigment termed vermilion and associated red mercury pigments.
Cinnabar generally occurs as a vein-filling mineral associated with volcanic activity and alkaline hot springs. The mineral resembles quartz in symmetry and it exhibits birefringence. Cinnabar has a mean refractive index near 3.2, a hardness between 2.0 and 2.5, and a specific gravity of approximately 8.1. The color and properties derive from a structure that is a hexagonal crystalline lattice belonging to the trigonal crystal system, crystals that sometimes exhibit twinning.
Cinnabar has been used for its color since antiquity in the Near East, including as a rouge-type cosmetic, in the New World since the Olmec culture, and in China since as early as the Yangshao culture, where it was used in coloring stoneware.
Associated modern precautions for the use and handling of cinnabar arise from the toxicity of the mercury component, which was recognized as early as ancient Rome. (Full article...) -
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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 21
Borax (also referred to as sodium borate, tincal (/ˈtɪŋkəl/) and tincar (/ˈtɪŋkər/)) is a salt (ionic compound), a hydrated or anhydrous borate of sodium, with the chemical formula Na2H20B4O17 (also written as Na2B4O7·10H2O).
It is a colorless crystalline solid that dissolves in water to make a basic solution.
It is commonly available in powder or granular form and has many industrial and household uses, including as a pesticide, as a metal soldering flux, as a component of glass, enamel, and pottery glazes, for tanning of skins and hides, for artificial aging of wood, as a preservative against wood fungus, and as a pharmaceutic alkalizer. In chemical laboratories, it is used as a buffering agent.
The terms tincal and tincar refer to native borax, historically mined from dry lake beds in various parts of Asia. (Full article...) -
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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 23
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 24
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 25
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...)
Selected mineralogist
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Image 1Sobolev, 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...)
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Charles Friedel (French: [fʁidɛl]; 12 March 1832 – 20 April 1899) was a French chemist and mineralogist. (Full article...) -
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Alexandre-Émile Béguyer de Chancourtois (20 January 1820 – 14 November 1886) was a French geologist and mineralogist who was the first to arrange the chemical elements in order of atomic weights, doing so in 1862. De Chancourtois only published his paper, but did not publish his actual graph with the irregular arrangement. Although his publication was significant, it was ignored by chemists as it was written in terms of geology. It was Dmitri Mendeleev's table published in 1869 that became most recognized. De Chancourtois was also a professor of mine surveying, and later geology at the École Nationale Supérieure des Mines de Paris. He also was the Inspector of Mines in Paris, and was widely responsible for implementing many mine safety regulations and laws during the time. (Full article...) -
Image 4
Ullmannite or Nickel glance (trivial name) is a nickel antimony sulfide mineral with formula: NiSbS. Considerable substitution occurs with cobalt and iron in the nickel site along with bismuth and arsenic in the antimony site. A solid solution series exists with the high cobalt willyamite. (Full article...) -
Image 5
William Phillips FGS FRS (10 May 1775 – 2 April 1828) was an English mineralogist and geologist. (Full article...) -
Image 6Sjur Aasmundsen Sexe (14 August 1808 – 17 February 1888) was a Norwegian mineralogist and educator. (Full article...)
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Image 7Adam August Krantz (6 December 1808 in Neumarkt in Schlesien – 6 April 1872 in Berlin) was a German mineralogist. (Full article...)
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Image 8Hendrik 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...) -
Image 9Adolf Knop (12 January 1828, in Altenau – 27 December 1893, in Karlsruhe) was a German geologist and mineralogist.
He studied mathematics and sciences at the University of Göttingen, where he was a pupil of chemist Friedrich Wohler and mineralogist Johann Friedrich Ludwig Hausmann. From 1849 he taught classes at the vocational school in Chemnitz. In 1857 he became an associate professor of geology and mineralogy at the University of Giessen, where in 1863 he attained a full professorship. In 1866 he relocated to Karlsruhe as a professor at the Polytechnic school. In 1878 he succeeded Moritz August Seubert as manager of the Grand Ducal Natural History Cabinet. (Full article...) -
Image 10
Henry Carvill Lewis (November 16, 1853 – July 21, 1888) was an American geologist and mineralogist. (Full article...) -
Image 11
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 12
William Hyde Wollaston FRS (/ˈwʊləstən/; 6 August 1766 – 22 December 1828) was an English chemist and physicist who is famous for discovering the chemical elements palladium and rhodium. He also developed a way to process platinum ore into malleable ingots. (Full article...) -
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Karl Cäsar von Leonhard (12 September 1779 in Rumpenheim – 23 January 1862 in Heidelberg) was a German mineralogist and geologist. His son, Gustav von Leonhard, was also a mineralogist.
From 1797 he studied at the universities of Marburg and Göttingen, where Johann Friedrich Blumenbach was an important influence to his career. He collected many mineralogical specimens on scientific excursions in Saxony and Thuringia, continued by travel to the Austrian Alps (including the Salzkammergut). During his journeys he made the acquaintance of Friedrich Mohs and Karl von Moll. In 1818, through assistance from Baden minister of state Sigismund von Reitzenstein, he was appointed professor of mineralogy at the University of Heidelberg. (Full article...) -
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Frédéric Cailliaud (9 June 1787 – 1 May 1869) was a French naturalist, mineralogist and conchologist. He was born, and died, in Nantes, where he was the curator of the Natural History Museum of Nantes from 1836 to 1869.
He travelled in Egypt, Nubia, and Ethiopia, collecting minerals and making observations. He was a part of the military expedition that his patron Viceroy Muhammad Ali sent south to conquer the Kingdom of Sennar, but also marched further into Fazogli where Caillaud searched for outcroppings of gold while the commander Ismail, son of Muhammad Ali, enslaved locals and slaughtered all who resisted him. Although he failed to find any sizeable deposits of gold in the mountains along the modern Sudan-Ethiopia border, he did make a sufficiently detailed survey of the area to be published after he returned to France in 1827. (Full article...) -
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Johann Friedrich August Breithaupt (May 16, 1791 – September 22, 1873) was a German mineralogist and professor at Freiberg Mining Academy in Freiberg, Saxony. (Full article...) -
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William Gregor (25 December 1761 – 11 June 1817) was an English clergyman and mineralogist who discovered the elemental metal titanium. (Full article...) -
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James Sowerby (21 March 1757 – 25 October 1822) was an English naturalist, illustrator and mineralogist. Contributions to published works, such as A Specimen of the Botany of New Holland or English Botany, include his detailed and appealing plates. The use of vivid colour and accessible texts was intended to reach a widening audience in works of natural history. The standard author abbreviation Sowerby is used to indicate this person as the author when citing a botanical name.[1] (Full article...) -
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Lars Fredrik Svanberg (13 May 1805 – 16 July 1878) was a Swedish chemist and mineralogist. (Full article...) -
Image 19
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 20Konrad Oebbeke (2 November 1853, Hildesheim – 1 February 1932) was a German geologist and mineralogist.
He studied at the Universities of Heidelberg and Erlangen, obtaining his doctorate at the University of Würzburg in 1877. Afterwards he worked as an assistant to the Geological Survey of Bavaria. He served as privat-docent at the University of Munich, later becoming a professor of mineralogy and geology at Erlangen (1887).
From 1895 to 1927 he was a professor at the Technische Hochschule of Munich. (Full article...) -
Image 21
Ernest-François Mallard (4 February 1833 – 6 July 1894) was a French mineralogist and a member of the French Academy of Sciences. He is also notable for his work with Henri Louis Le Chatelier in combustion as applied to mining safety. (Full article...) -
Image 22
Nikolay Vasilyevich Belov (Russian: Никола́й Васи́льевич Бело́в; December 14, 1891 – March 6, 1982) was a Soviet and Russian crystallographer, geochemist, academician (1953), and Hero of Socialist Labour (1969).
Belov worked primarily in the fields of mineralogy (particularly silicates), determination of crystal structures using X-ray crystallography, and the theory of symmetry, specifically dichromatic, and polychromatic symmetry, a field which Belov founded. (Full article...) -
Image 23George "Shavey" Lorenzo Noyes (August 30, 1863 – 1945) was an American mineralogist, naturalist, development critic, writer and landscape artist. (Full article...)
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Image 24Marjorie Hooker (10 May 1908 – 4 May 1976) was an American geologist who worked to collect data on the make-up of igneous and metamorphic rocks as well as acted as a mineral specialist for the United States Department of State from 1943 to 1947. Her work on deciphering chemical data for granite rocks led her to collect and correspond information with geologists from all around the world. The multiple associations with which she worked include the American Association for the Advancement of Science, the Washington Academy of Sciences, the Geological Society of London, the Mineralogical Society of Great Britain and Ireland, the American Geophysical Union, the Geological Society of America, and the Mineralogical Association of Canada. She also worked as a delegate of the International Geological Congresses for their 19th, 20th, 23rd, and 24th meetings. Her contributions to Geology have been recognized with an award created in her name at Syracuse University to recognize and aid exceptional student research. (Full article...)
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William Babington FRS FGS (21 May 1756 – 29 April 1833) was an Anglo-Irish physician and mineralogist. (Full article...)
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General images
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Image 1Pink 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 2Schist 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 3When 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 6Red cinnabar (HgS), a mercury ore, on dolomite. (from Mineral)
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Image 8Native 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 11Black andradite, an end-member of the orthosilicate garnet group. (from Mineral)
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Image 12Gypsum desert rose (from Mineral)
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Image 14Asbestiform tremolite, part of the amphibole group in the inosilicate subclass (from Mineral)
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Image 15An example of elbaite, a species of tourmaline, with distinctive colour banding. (from Mineral)
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Image 17Hübnerite, the manganese-rich end-member of the wolframite series, with minor quartz in the background (from Mineral)
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Image 18Perfect basal cleavage as seen in biotite (black), and good cleavage seen in the matrix (pink orthoclase). (from Mineral)
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Image 19Epidote often has a distinctive pistachio-green colour. (from Mineral)
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Image 20Sphalerite crystal partially encased in calcite from the Devonian Milwaukee Formation of Wisconsin (from Mineral)
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Image 21Mohs Scale versus Absolute Hardness (from Mineral)
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Image 24Diamond is the hardest natural material, and has a Mohs hardness of 10. (from Mineral)
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Image 25Mohs hardness kit, containing one specimen of each mineral on the ten-point hardness scale (from Mohs scale)
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Image 26Muscovite, a mineral species in the mica group, within the phyllosilicate subclass (from Mineral)
In the news
- 3 May 2024 –
- Panama bans First Quantum Minerals from extracting copper following the closure of its Cobre Panamá mine last year. (Reuters) (The Globe and Mail)
Did you know ...?
- ... that the rare mineral Matlockite (PbFCl) (pictured) is named after a town in Derbyshire?
- ...that the amorphous phosphate mineral santabarbaraite was named after the Italian mining district Santa Barbara where it was discovered in 2003, but its name also honors Saint Barbara, the patron saint of miners?
- ...that when yellow crystals of mosesite, a very rare mineral found in deposits of mercury, are heated to 186 °C (367 °F), they become isotropic?
Subcategories
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Topics
Overview | ||
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Common minerals |
Ore minerals, mineral mixtures and ore deposits | |||||||||
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Ores |
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Deposit types |
Borates | |||||
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Carbonates | |||||
Oxides |
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Phosphates | |||||
Silicates | |||||
Sulfides | |||||
Other |
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Crystalline | |||||||
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Cryptocrystalline | |||||||
Amorphous | |||||||
Miscellaneous | |||||||
Notable varieties |
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Oxide minerals |
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Silicate minerals | |||||
Other |
Gemmological classifications by E. Ya. Kievlenko (1980), updated | |||||||||
Jewelry stones |
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Jewelry-Industrial stones |
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Industrial stones |
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Mineral identification | |
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"Special cases" ("native elements and organic minerals") |
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"Sulfides and oxides" |
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"Evaporites and similars" |
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"Mineral structures with tetrahedral units" (sulfate anion, phosphate anion, silicon, etc.) |
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