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, and their utilization. (Full article...)
Selected articles
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Image 1

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 2
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.
It occurs mostly in association with calcite, quartz, smoky quartz, hematite, pyrite, fluorite, goethite, agate, and chalcedony. (Full article...) -
Image 3

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.
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.
Like most other opaque gems, turquoise has been devalued by the introduction of treatments, imitations, and synthetics into the market. (Full article...) -
Image 4

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 5

Crystal structure of table salt (sodium in purple, chlorine in green)
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 constituent particles to form symmetric patterns that repeat along the principal directions of three-dimensional space in matter.
The smallest group of particles in a 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 principal axes/edges, of the unit cell and angles between them are lattice constants, also called lattice parameters or cell parameters. The symmetry properties of a crystal are described by the concept of space groups. All possible symmetric arrangements of particles in three-dimensional space may be described by 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 6A 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 7

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 8

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 as in emerging developments in these fields. (Full article...) -
Image 9

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...) -
Image 10Malachite from the Democratic Republic of the Congo
Malachite (/ˈmæl.əˌkaɪt/) 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 11
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 12
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...) -
Image 13

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...) -
Image 14

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, and their utilization. (Full article...) -
Image 15
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 crystal structure geometry it forms a complete solid solution at temperatures above 950 °C (1,740 °F).
Hematite occurs naturally 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. The term kidney ore may be broadly used to describe botryoidal, mammillary, or reniform hematite. 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 may 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 also may 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 16Quartz crystal cluster from Brazil
Quartz is a hard mineral composed of silica (silicon dioxide). Its atoms are linked in a continuous framework of SiO4 silicon–oxygen tetrahedra, with each oxygen atom being shared between two tetrahedra, giving an overall chemical formula of SiO2. Therefore, quartz is classified structurally as a framework silicate mineral and compositionally as an oxide mineral. Quartz is the second most common mineral or mineral group in Earth's lithosphere, comprising about 12% by mass.
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 17
Diamond is a solid form of the element carbon with its atoms arranged in a crystal structure called diamond cubic. Diamond is tasteless, odorless, strong, brittle solid, colorless 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.
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 18Cinnabar, Staatliches Museum für Naturkunde Karlsruhe, Germany
Cinnabar (/ˈsɪnəˌbɑːr/; from Ancient Greek κιννάβαρι (kinnábari)), also called cinnabarite (/ˌsɪnəˈbɑːraɪt/) or 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 19

Frameworks of LTA-type (left) and FAU-type zeolites (right)
Zeolites are a group of several microporous, crystalline aluminosilicate minerals commonly used as commercial adsorbents and catalysts. They mainly consist of silicon, aluminium, and 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+.
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". (Full article...) -
Image 20
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.
As hydroxyapatite, it forms a major part of the teeth and bones of vertebrate animals. (Full article...) -
Image 21

The diamond crystal structure belongs to the face-centered cubic lattice, with a repeated two-atom pattern.
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 (an infinite array of discrete points). Space groups (symmetry groups of a configuration in space) 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 22The 423-carat (85 g) blue Logan Sapphire
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 the 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. It occurs in association with ruby, zircon, biotite, muscovite, calcite, dravite and quartz. (Full article...) -
Image 23A ruby crystal from Dodoma Region, Tanzania
Ruby is a pinkish-red to blood-red gemstone, a variety of the mineral corundum (aluminium oxide). Ruby is one of the most popular traditional jewelry gems and is very durable. Other varieties of gem-quality corundum are called sapphires; given that the rest of the corundum species are called as such, rubies are sometimes referred to as "red sapphires".
Ruby is one of the traditional cardinal gems, alongside amethyst, sapphire, emerald, and diamond. The word ruby comes from ruber, Latin for red. The color of a ruby is due to the presence of chromium.
Some gemstones that are popularly or historically called rubies, such as the Black Prince's Ruby in the British Imperial State Crown, are actually spinels. These were once known as "Balas rubies".
The quality of a ruby is determined by its color, cut, and clarity, which, along with carat weight, affect its value. The brightest and most valuable shade of red, called blood-red or pigeon blood, commands a large premium over other rubies of similar quality. After color comes clarity: similar to diamonds, a clear stone will command a premium, but a ruby without any needle-like rutile inclusions may indicate that the stone has been treated. Ruby is the traditional birthstone for July and is usually pinker than garnet, although some rhodolite garnets have a similar pinkish hue to most rubies. The world's most valuable ruby to be sold at auction is the Estrela de Fura, which sold for US$34.8 million. (Full article...) -
Image 24
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...) -
Image 25Deep 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...)
Selected mineralogist
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Image 1

Der Mineraloge (The Mineralogist) by Raphael Ritz, 1883. Thought to depict the Bonn mineralogist Gerhard vom Rath (1830-1888), examining mineral specimens from Lengenbach in a nearby house in Binn, Switzerland
Gerhard vom Rath (20 August 1830 – 23 April 1888), was a German mineralogist, born at Duisburg in Prussia. (Full article...) -
Image 2
Vladimir Stepanovich Sobolev (Russian: Владимир Степанович Соболев; 30 May 1908 – 1 September 1982) was a Soviet geologist, petrologist and mineralogist, Academician of the USSR Academy of Sciences (1966), Hero of Socialist Labour (1978), and laureate of the Lenin Prize and the Stalin Prize.
He was one of the founders of modern Soviet petrology and metamorphic geology and a pioneer in applying facies concepts to large-scale geological mapping. Sobolev was the first to predict the presence of diamond-bearing kimberlites in Eastern Siberia, a forecast later confirmed by discoveries in the 1950s. (Full article...) -
Image 3Vladimir Vital'evich Shcherbina (1907–1978) was a prominent Soviet geochemist and mineralogist. He was a student of Alexander Fersman.
In 1931, he led a team from the USSR Academy of Sciences in the mineralogical examination of the Lovozero Massif. (Full article...) -
Image 4

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 5Walter Frederick Ferrier (1865–1950) was a Canadian geologist and mining engineer.
He graduated from McGill University's school of mining engineering. He was a tireless mineral collector and was known for walking straight into mining offices to request specimens. Consequently, he created large collections of mineral specimens of a quality still admired to this day. Many classic specimens would never be in collections had it not been for his effort and skill.
The mineral specimens he amassed were instrumental in creating the mineral collections of the Smithsonian in Washington DC, the Royal Ontario Museum in Toronto, Ontario, Canada, University of Alberta, and the museum particularly dear to his heart, the Redpath Museum at McGill University in Montreal, Quebec, Canada. (Full article...) -
Image 6

Wilhelm Karl Haidinger (5 February 1795 – 19 March 1871), ennobled as Wilhelm Ritter von Haidinger in 1864, was an Austrian mineralogist. (Full article...) -
Image 7James Freeman Dana (born in Amherst, New Hampshire, 23 September 1793; died in New York City, 14 April 1827) was an American chemist. (Full article...)
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Image 8

Hubert Curien (30 October 1924 – 6 February 2005) was a French physicist and a key figure in European science politics, as the President of CERN Council (1994–1996), the first chairman of the European Space Agency (ESA) (1981–1984), and second President of the Academia Europæa and a President of Fondation de France. (Full article...) -
Image 9

Johann Reinhard Blum, c. 1860
Johann Reinhard Blum (28 October 1802, Hanau – 21 August 1883, Heidelberg) was a German mineralogist.
From 1821 he studied at the universities of Heidelberg and Marburg, receiving his habilitation for mineralogy in 1828. In 1838 he became an associate professor, and in 1856, a full professor of mineralogy at the University of Heidelberg. For many years he was director of the university's mineral collection. In 1871 he was a founding member of the Oberrheinischen Geologischen Vereins (Upper Rhine Geological Association). (Full article...) -
Image 10Carlo Perrier (born 7 July 1886 in Turin; died 22 May 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...) -
Image 11Josef Zemann (25 May 1923 – 16 October 2022) was an Austrian mineralogist and geologist. (Full article...)
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Gaius Plinius Secundus (23 or 24 CE - 25 August 79 CE), known in English as Pliny the Elder (/ˈplɪni/ PLIN-ee), was a Roman author, naturalist, scientist, naval and army commander of the early Roman Empire, and friend of the emperor Vespasian. Pliny wrote the encyclopedic Naturalis Historia (Natural History), a comprehensive thirty-seven-volume work covering a vast array of topics on human knowledge and the natural world, 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[according to whom?] was the twenty-volume Bella Germaniae ("Wars of Germania"), which is no longer extant. Bella Germaniae, which began where Aufidius Bassus' writings on Germani wars 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 Germani"). (Full article...) -
Image 13Hans Morten Thrane Esmark (21 August 1801 – 24 April 1882) was a Norwegian priest and mineralogist. He is most noted for first locating the mineral thorite. (Full article...)
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Anton Schrötter von Kristelli (26 November 1802 – 15 April 1875) was an Austrian chemist and mineralogist born in Olomouc, Moravia. His son Leopold Schrötter Ritter von Kristelli (1837–1908) was a noted laryngologist. (Full article...) -
Image 15William Sansom Vaux (May 19, 1811 – May 5, 1882) was an American mineralogist. He served as vice-president of the Academy of Natural Sciences in Philadelphia from 1864 to 1882 and as president of the Zoological Society of Philadelphia. His mineral and archaeological collections were bequeathed to the Academy of Natural Sciences after his death. (Full article...)
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George Gibbs (January 7, 1776 – August 6, 1833) was an American mineralogist and mineral collector. The mineral gibbsite is named after him. (Full article...) -
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Charles-Louis de la Vallée Poussin
Charles-Louis-Joseph-Xavier de la Vallée Poussin (6 April 1827, Namur – 15 March 1903, Brussels) was a Belgian geologist and mineralogist. His son was the mathematician Charles Jean de la Vallée Poussin. (Full article...) -
Image 18Alexander Karl von Kraatz-Koschlau (24 June 1867 – 18 May 1900) was a German geologist.
Karl von Kraatz-Koschlau was born in Reichenbach near Stettin. He studied philosophy and sciences in Freiburg and Munich, where he obtained his doctorate with a dissertation on tartaric acid and its salts (1892). Afterwards he was assigned to the mineralogical institute in Munich. One of his scientific excursions during this time period involved geological research of the Serra de Monchique in the Algarve. (Full article...) -
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William Walter Jefferis (January 12, 1820 – February 23, 1906) was an American mineralogist and curator of the William S. Vaux Collection of minerals and artifacts at the Philadelphia Academy of Natural Sciences from 1883 to 1898. He personally collected and cataloged 35,000 mineral specimens, which he sold to the Carnegie Museum of Natural History in 1905. (Full article...) -
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Johann Friedrich Ludwig Hausmann
Johann Friedrich Ludwig Hausmann (22 February 1782 – 26 December 1859) was a German mineralogist. (Full article...) -
Image 21Julian Royce Goldsmith (1918–1999) was a mineralogist and geochemist at the University of Chicago (Moore, 1971). Goldsmith, along with colleague Fritz Laves, first defined the crystallographic polymorphism of alkali feldspar (Newton, 1989). Goldsmith also experimented on the temperature dependence of the solid solution between calcite and dolomite (Newton, 1989). Goldsmith's research also led him to experiment with the determination of the stability of intermediate structural states of albite (Newton, 1989). For his outstanding contributions to the study of mineralogy and geochemistry, Goldsmith was awarded the prestigious Roebling Medal by the Mineralogical Society of America in 1988 (Newton, 1989). The mineral julgoldite was named for him. (Full article...)
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Image 22

Petru Poni (4 January 1841 – 2 April 1925) was a Romanian chemist and mineralogist.
Born into a family of răzeși (free peasants) in Săcărești, Iași County, he attended primary school in Târgu Frumos. In 1852, he enrolled in Academia Mihăileană; among his teachers were August Treboniu Laurian and Simion Bărnuțiu. He entered the University of Paris in 1865, studying chemistry there. He returned home following graduation, teaching physics and chemistry at Iași's National College and at the military high school. In 1878, he became a professor at the University of Iași, at first teaching at the medicine and science faculties, later only in the mineral chemistry department of the latter. He served as Religious Affairs and Education Minister three times: in 1891, 1895–1896 and in 1918. A bitter rival of his was the Conservative Titu Maiorescu, and he was obliged to leave the Liberal cabinet in 1896 after a dispute related to the Romanian Orthodox Church. When not in government, he continued to work in his chemistry laboratory in Iași. (Full article...) -
Image 23Portrait by Joseph Karl Stieler, 1828
Johann Wolfgang von Goethe (28 August 1749 – 22 March 1832) was a German polymath who is widely regarded as the most influential writer in the German language. His work has had a wide-ranging influence on literary, political, and philosophical thought in the Western world from the late 18th century to the present. A poet, playwright, novelist, scientist, statesman, theatre-director, and critic, Goethe wrote a wide range of works, including plays, poetry and aesthetic criticism, as well as treatises on botany, anatomy, and colour.
Goethe took up residence in Weimar in 1775 following the success of his first novel, The Sorrows of Young Werther (1774), and joined a thriving intellectual and cultural environment under the patronage of Duchess Anna Amalia that formed the basis of Weimar Classicism. He was ennobled by Karl August, Duke of Saxe-Weimar, in 1782. Goethe was an early participant in the Sturm und Drang literary movement. During his first ten years in Weimar, Goethe became a member of the Duke's privy council (1776–1785), sat on the war and highway commissions, oversaw the reopening of silver mines in nearby Ilmenau, and implemented a series of administrative reforms at the University of Jena. He also contributed to the planning of Weimar's botanical park and the rebuilding of its Ducal Palace. (Full article...) -
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George Jarvis Brush (December 15, 1831 – February 5, 1912) was an American mineralogist and academic administrator who spent most of his career at Yale University in the Sheffield Scientific School. (Full article...) -
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Christian Samuel Weiss (26 February 1780 – 1 October 1856) was a German mineralogist born in Leipzig.
Following graduation, he worked as a physics instructor in Leipzig from 1803 until 1808. and in the meantime, conducted geological studies of mountain formations in Tyrol, Switzerland and France (1806–08). In 1810 he became a professor of mineralogy at the University of Berlin, where in 1818/19 and 1832/33, he served as university rector. He died near Eger in Bohemia. (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 1Muscovite, a mineral species in the mica group, within the phyllosilicate subclass (from Mineral)
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Image 4An example of elbaite, a species of tourmaline, with distinctive colour banding. (from Mineral)
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Image 5Schist 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 6Mohs hardness kit, containing one specimen of each mineral on the ten-point hardness scale (from Mohs scale)
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Image 7When 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 8Asbestiform tremolite, part of the amphibole group in the inosilicate subclass (from Mineral)
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Image 9Sphalerite crystal partially encased in calcite from the Devonian Milwaukee Formation of Wisconsin (from Mineral)
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Image 11Diamond is the hardest natural material, and has a Mohs hardness of 10. (from Mineral)
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Image 12Red cinnabar (HgS), a mercury ore, on dolomite. (from Mineral)
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Image 15Pink 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 16Gypsum desert rose (from Mineral)
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Image 17Epidote often has a distinctive pistachio-green colour. (from Mineral)
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Image 20Hübnerite, the manganese-rich end-member of the wolframite series, with minor quartz in the background (from Mineral)
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Image 21Native 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 22Black andradite, an end-member of the orthosilicate garnet group. (from Mineral)
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Image 25Perfect basal cleavage as seen in biotite (black), and good cleavage seen in the matrix (pink orthoclase). (from Mineral)
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Image 26Mohs Scale versus Absolute Hardness (from Mineral)
Did you know ...?
- ... that after a mine tunnel was dug near Cerro de Pasco, Peru, the first known specimen of pascoite (example pictured) formed on the walls?
- ... that the name of mineral scrutinyite reflects the efforts spent to distinguish it from plattnerite – another form of lead dioxide?
- ... that the crystal symmetry of melanophlogite changes depending on the guests trapped inside it?
- ... that the mineral messelite was described in 1890, discredited in 1940, reinstated and named neomesselite in 1955, and named messelite once again by 1959?
Subcategories
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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