Portal:Minerals

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...)

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$Image 1 A crystalline solid: atomic resolution image of strontium titanate. Brighter spots are columns of strontium atoms and darker ones are titanium-oxygen columns. Crystallography is the branch of science devoted to the study of molecular and crystalline structure and properties. The word crystallography is derived from the Ancient Greek word κρύσταλλος (krústallos; "clear ice, rock-crystal"), and γράφειν (gráphein; "to write"). In July 2012, the United Nations recognised the importance of the science of crystallography by proclaiming 2014 the International Year of Crystallography. Crystallography is a broad topic, and many of its subareas, such as X-ray crystallography, are themselves important scientific topics. Crystallography ranges from the fundamentals of crystal structure to the mathematics of crystal geometry, including those that are not periodic or quasicrystals. At the atomic scale it can involve the use of X-ray diffraction to produce experimental data that the tools of X-ray crystallography can convert into detailed positions of atoms, and sometimes electron density. At larger scales it includes experimental tools such as orientational imaging to examine the relative orientations at the grain boundary in materials. Crystallography plays a key role in many areas of biology, chemistry, and physics, as well new developments in these fields. (Full article...)$

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A crystalline solid: atomic resolution image of strontium titanate. Brighter spots are columns of strontium atoms and darker ones are titanium-oxygen columns.

Crystallography is the branch of science devoted to the study of molecular and crystalline structure and properties. The word crystallography is derived from the Ancient Greek word κρύσταλλος (krústallos; "clear ice, rock-crystal"), and γράφειν (gráphein; "to write"). In July 2012, the United Nations recognised the importance of the science of crystallography by proclaiming 2014 the International Year of Crystallography.

Crystallography is a broad topic, and many of its subareas, such as X-ray crystallography, are themselves important scientific topics. Crystallography ranges from the fundamentals of crystal structure to the mathematics of crystal geometry, including those that are not periodic or quasicrystals. At the atomic scale it can involve the use of X-ray diffraction to produce experimental data that the tools of X-ray crystallography can convert into detailed positions of atoms, and sometimes electron density. At larger scales it includes experimental tools such as orientational imaging to examine the relative orientations at the grain boundary in materials. Crystallography plays a key role in many areas of biology, chemistry, and physics, as well new developments in these fields. (Full article...)
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A 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 Zr SiO₄. An empirical formula showing some of the range of substitution in zircon is (Zr_1–y, REE_y)(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...)
$Image 3 Rutile is an oxide mineral composed of titanium dioxide (TiO2), the most common natural form of TiO2. Rarer polymorphs of TiO2 are known, including anatase, akaogiite, and brookite. Rutile has one of the highest refractive indices at visible wavelengths of any known crystal and also exhibits a particularly large birefringence and high dispersion. Owing to these properties, it is useful for the manufacture of certain optical elements, especially polarization optics, for longer visible and infrared wavelengths up to about 4.5 micrometres. Natural rutile may contain up to 10% iron and significant amounts of niobium and tantalum. Rutile derives its name from the Latin rutilus ('red'), in reference to the deep red color observed in some specimens when viewed by transmitted light. Rutile was first described in 1803 by Abraham Gottlob Werner using specimens obtained in Horcajuelo de la Sierra, Madrid (Spain), which is consequently the type locality. (Full article...)$

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Rutile is an oxide mineral composed of titanium dioxide (TiO₂), the most common natural form of TiO₂. Rarer polymorphs of TiO₂ are known, including anatase, akaogiite, and brookite.

Rutile has one of the highest refractive indices at visible wavelengths of any known crystal and also exhibits a particularly large birefringence and high dispersion. Owing to these properties, it is useful for the manufacture of certain optical elements, especially polarization optics, for longer visible and infrared wavelengths up to about 4.5 micrometres. Natural rutile may contain up to 10% iron and significant amounts of niobium and tantalum.

Rutile derives its name from the Latin rutilus ('red'), in reference to the deep red color observed in some specimens when viewed by transmitted light. Rutile was first described in 1803 by Abraham Gottlob Werner using specimens obtained in Horcajuelo de la Sierra, Madrid (Spain), which is consequently the type locality. (Full article...)
$Image 4 A rich seam of iridescent opal encased in matrix Opal is a hydrated amorphous form of silica (SiO2·nH2O); its water content may range from 3% to 21% by weight, but is usually between 6% and 10%. Due to the amorphous (chemical) physical structure, it is classified as a mineraloid, unlike crystalline forms of silica, which are considered minerals. It is deposited at a relatively low temperature and may occur in the fissures of almost any kind of rock, being most commonly found with limonite, sandstone, rhyolite, marl, and basalt. The name opal is believed to be derived from the Sanskrit word upala (उपल), which means 'jewel', and later the Greek derivative opállios (ὀπάλλιος). There are two broad classes of opal: precious and common. Precious opal displays play-of-color (iridescence); common opal does not. Play-of-color is defined as "a pseudo chromatic optical effect resulting in flashes of colored light from certain minerals, as they are turned in white light." The internal structure of precious opal causes it to diffract light, resulting in play-of-color. Depending on the conditions in which it formed, opal may be transparent, translucent, or opaque, and the background color may be white, black, or nearly any color of the visual spectrum. Black opal is considered the rarest, while white, gray, and green opals are the most common. (Full article...)$

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A rich seam of iridescent opal encased in matrix

Opal is a hydrated amorphous form of silica (SiO₂·nH₂O); its water content may range from 3% to 21% by weight, but is usually between 6% and 10%. Due to the amorphous (chemical) physical structure, it is classified as a mineraloid, unlike crystalline forms of silica, which are considered minerals. It is deposited at a relatively low temperature and may occur in the fissures of almost any kind of rock, being most commonly found with limonite, sandstone, rhyolite, marl, and basalt.

The name opal is believed to be derived from the Sanskrit word upala (उपल), which means 'jewel', and later the Greek derivative opállios (ὀπάλλιος).

There are two broad classes of opal: precious and common. Precious opal displays play-of-color (iridescence); common opal does not. Play-of-color is defined as "a pseudo chromatic optical effect resulting in flashes of colored light from certain minerals, as they are turned in white light." The internal structure of precious opal causes it to diffract light, resulting in play-of-color. Depending on the conditions in which it formed, opal may be transparent, translucent, or opaque, and the background color may be white, black, or nearly any color of the visual spectrum. Black opal is considered the rarest, while white, gray, and green opals are the most common. (Full article...)
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Magnetite from Bolivia

Magnetite is a mineral and one of the main iron ores, with the chemical formula Fe²⁺Fe3+2O₄. It is one of the oxides of iron, and is ferrimagnetic; it is attracted to a magnet and can be magnetized to become a permanent magnet itself. With the exception of extremely rare native iron deposits, it is the most magnetic of all the naturally occurring minerals on Earth. Naturally magnetized pieces of magnetite, called lodestone, will attract small pieces of iron, which is how ancient peoples first discovered the property of magnetism.

Magnetite is black or brownish-black with a metallic luster, has a Mohs hardness of 5–6 and leaves a black streak. Small grains of magnetite are very common in igneous and metamorphic rocks.

The chemical IUPAC name is iron(II,III) oxide and the common chemical name is ferrous-ferric oxide. (Full article...)
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Corundum is a crystalline form of aluminium oxide (Al₂O₃) typically containing traces of iron, titanium, vanadium, and chromium. It is a rock-forming mineral. It is a naturally transparent material, but can have different colors depending on the presence of transition metal impurities in its crystalline structure. Corundum has two primary gem varieties: ruby and sapphire. Rubies are red due to the presence of chromium, and sapphires exhibit a range of colors depending on what transition metal is present. A rare type of sapphire, padparadscha sapphire, is pink-orange.

The name "corundum" is derived from the Tamil-Dravidian word kurundam (ruby-sapphire) (appearing in Sanskrit as kuruvinda).

Because of corundum's hardness (pure corundum is defined to have 9.0 on the Mohs scale), it can scratch almost all other minerals. Emery, a variety of corundum with no value as a gemstone, is commonly used as an abrasive on sandpaper and on large tools used in machining metals, plastics, and wood. It is a black granular form of corundum, in which the mineral is intimately mixed with magnetite, hematite, or hercynite.

In addition to its hardness, corundum has a density of 4.02 g/cm³ (251 lb/cu ft), which is unusually high for a transparent mineral composed of the low-atomic mass elements aluminium and oxygen. (Full article...)
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A rock containing three crystals of pyrite (FeS₂). The crystal structure of pyrite is primitive cubic, and this is reflected in the cubic symmetry of its natural crystal facets.

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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Intergrowth of lustrous, cubic crystals of pyrite, with some surfaces showing characteristic striations, from Huanzala mine, Ancash, Peru. Specimen size: 7.0 × 5.0 × 2.5 cm

The mineral pyrite (/ˈpaɪraɪt/ PY-ryte), or iron pyrite, also known as fool's gold, is an iron sulfide with the chemical formula Fe S₂ (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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Fibrous tremolite asbestos on muscovite

Asbestos (/æsˈbɛstəs, æz-, -tɒs/ ass-BES-təs, az-, -⁠toss) is a group of naturally occurring, toxic, carcinogenic and fibrous silicate minerals. There are six types, all of which are composed of long and thin fibrous crystals, each fibre (particulate with length substantially greater than width) being composed of many microscopic "fibrils" that can be released into the atmosphere by abrasion and other processes. Inhalation of asbestos fibres can lead to various dangerous lung conditions, including mesothelioma, asbestosis, and lung cancer. As a result of these health effects, asbestos is considered a serious health and safety hazard.

Archaeological studies have found evidence of asbestos being used as far back as the Stone Age to strengthen ceramic pots, but large-scale mining began at the end of the 19th century when manufacturers and builders began using asbestos for its desirable physical properties. Asbestos is an excellent thermal and electrical insulator, and is highly fire resistant, so for much of the 20th century, it was very commonly used around the world as a building material (particularly for its fire-retardant properties), until its adverse effects on human health were more widely recognized and acknowledged in the 1970s. Many buildings constructed before the 1980s contain asbestos.

The use of asbestos for construction and fireproofing has been made illegal in many countries. Despite this, around 255,000 people are thought to die each year from diseases related to asbestos exposure. In part, this is because many older buildings still contain asbestos; in addition, the consequences of exposure can take decades to arise. The latency period (from exposure until the diagnosis of negative health effects) is typically 20 years. The most common diseases associated with chronic asbestos exposure are asbestosis (scarring of the lungs due to asbestos inhalation) and mesothelioma (a type of cancer).

Many developing countries still support the use of asbestos as a building material, and mining of asbestos is ongoing, with the top producer, Russia, having an estimated production of 790,000 tonnes in 2020. (Full article...)
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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...)
$Image 11 Graphite specimen Graphite (/ˈɡræfaɪt/) is a crystalline allotrope (form) of the element carbon. It consists of many stacked layers of graphene, typically in excess of hundreds of layers. Graphite occurs naturally and is the most stable form of carbon under standard conditions. Synthetic and natural graphite are consumed on a large scale (1.3 million metric tons per year in 2022) for uses in many critical industries including refractories (50%), lithium-ion batteries (18%), foundries (10%), and lubricants (5%), among others (17%). Under extremely high pressures and extremely high temperatures it converts to diamond. Graphite's low cost, thermal and chemical inertness and characteristic conductivity of heat and electricity finds numerous applications in high energy and high temperature processes. (Full article...)$

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Graphite specimen

Graphite (/ˈɡræfaɪt/) is a crystalline allotrope (form) of the element carbon. It consists of many stacked layers of graphene, typically in excess of hundreds of layers. Graphite occurs naturally and is the most stable form of carbon under standard conditions. Synthetic and natural graphite are consumed on a large scale (1.3 million metric tons per year in 2022) for uses in many critical industries including refractories (50%), lithium-ion batteries (18%), foundries (10%), and lubricants (5%), among others (17%). Under extremely high pressures and extremely high temperatures it converts to diamond. Graphite's low cost, thermal and chemical inertness and characteristic conductivity of heat and electricity finds numerous applications in high energy and high temperature processes. (Full article...)
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Kaolinite (/ˈkeɪ.ələˌnaɪt, -lɪ-/ KAY-ə-lə-nyte, -⁠lih-; also called kaolin) is a clay mineral, with the chemical composition Al₂Si₂O₅(OH)₄. It is a layered silicate mineral, with one tetrahedral sheet of silica (SiO₄) linked through oxygen atoms to one octahedral sheet of alumina (AlO₆).

Kaolinite is a soft, earthy, usually white, mineral (dioctahedral phyllosilicate clay), produced by the chemical weathering of aluminium silicate minerals like feldspar. It has a low shrink–swell capacity and a low cation-exchange capacity (1–15 meq/100 g).

Rocks that are rich in kaolinite, and halloysite, are known as kaolin (/ˈkeɪ.əlɪn/) or china clay. In many parts of the world kaolin is colored pink-orange-red by iron oxide, giving it a distinct rust hue. Lower concentrations of iron oxide yield the white, yellow, or light orange colors of kaolin. Alternating lighter and darker layers are sometimes found, as at Providence Canyon State Park in Georgia, United States.

Kaolin is an important raw material in many industries and applications. Commercial grades of kaolin are supplied and transported as powder, lumps, semi-dried noodle or slurry. Global production of kaolin in 2021 was estimated to be 45 million tonnes, with a total market value of US $4.24 billion. (Full article...)
$Image 13 Talc, or talcum, is a clay mineral composed of hydrated magnesium silicate, with the chemical formula Mg3Si4O10(OH)2. Talc in powdered form, often combined with corn starch, is used as baby powder. This mineral is used as a thickening agent and lubricant. It is an ingredient in ceramics, paints, and roofing material. It is a main ingredient in many cosmetics. It occurs as foliated to fibrous masses, and in an exceptionally rare crystal form. It has a perfect basal cleavage and an uneven flat fracture, and it is foliated with a two-dimensional platy form. The Mohs scale of mineral hardness, based on scratch hardness comparison, defines value 1 as the hardness of talc, the softest mineral. When scraped on a streak plate, talc produces a white streak, though this indicator is of little importance, because most silicate minerals produce a white streak. Talc is translucent to opaque, with colors ranging from whitish grey to green with a vitreous and pearly luster. Talc is not soluble in water, and is slightly soluble in dilute mineral acids. Soapstone is a metamorphic rock composed predominantly of talc. (Full article...)$

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Talc, or talcum, is a clay mineral composed of hydrated magnesium silicate, with the chemical formula Mg₃Si₄O₁₀(OH)₂. Talc in powdered form, often combined with corn starch, is used as baby powder. This mineral is used as a thickening agent and lubricant. It is an ingredient in ceramics, paints, and roofing material. It is a main ingredient in many cosmetics. It occurs as foliated to fibrous masses, and in an exceptionally rare crystal form. It has a perfect basal cleavage and an uneven flat fracture, and it is foliated with a two-dimensional platy form.

The Mohs scale of mineral hardness, based on scratch hardness comparison, defines value 1 as the hardness of talc, the softest mineral. When scraped on a streak plate, talc produces a white streak, though this indicator is of little importance, because most silicate minerals produce a white streak. Talc is translucent to opaque, with colors ranging from whitish grey to green with a vitreous and pearly luster. Talc is not soluble in water, and is slightly soluble in dilute mineral acids.

Soapstone is a metamorphic rock composed predominantly of talc. (Full article...)
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Galena with minor pyrite

Galena, also called lead glance, is the natural mineral form of lead(II) sulfide (PbS). It is the most important ore of lead and an important source of silver.

Galena is one of the most abundant and widely distributed sulfide minerals. It crystallizes in the cubic crystal system often showing octahedral forms. It is often associated with the minerals sphalerite, calcite and fluorite.

As a pure specimen held in the hand, under standard temperature and pressure, galena is insoluble in water and so is almost non-toxic. Handling galena under these specific conditions (such as in a museum or as part of geology instruction) poses practically no risk; however, as lead(II) sulfide is reasonably reactive in a variety of environments, it can be highly toxic if swallowed or inhaled, particularly under prolonged or repeated exposure. (Full article...)
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Halite from the Wieliczka salt mine, Małopolskie, Poland

Halite (/ˈhælaɪt, ˈheɪlaɪt/ HAL-yte, HAY-lyte), commonly known as rock salt, is a type of salt, the mineral (natural) form of sodium chloride (Na Cl). 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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Green fluorite with prominent cleavage

Cleavage, in mineralogy and materials science, is the tendency of crystalline materials to split along definite crystallographic structural planes. These planes of relative weakness are a result of the regular locations of atoms and ions in the crystal, which create smooth repeating surfaces that are visible both in the microscope and to the naked eye. If bonds in certain directions are weaker than others, the crystal will tend to split along the weakly bonded planes. These flat breaks are termed "cleavage". The classic example of cleavage is mica, which cleaves in a single direction along the basal pinacoid, making the layers seem like pages in a book. In fact, mineralogists often refer to "books of mica".

Diamond and graphite provide examples of cleavage. Each is composed solely of a single element, carbon. In diamond, each carbon atom is bonded to four others in a tetrahedral pattern with short covalent bonds. The planes of weakness (cleavage planes) in a diamond are in four directions, following the faces of the octahedron. In graphite, carbon atoms are contained in layers in a hexagonal pattern where the covalent bonds are shorter (and thus even stronger) than those of diamond. However, each layer is connected to the other with a longer and much weaker van der Waals bond. This gives graphite a single direction of cleavage, parallel to the basal pinacoid. So weak is this bond that it is broken with little force, giving graphite a slippery feel as layers shear apart. As a result, graphite makes an excellent dry lubricant.

While all single crystals will show some tendency to split along atomic planes in their crystal structure, if the differences between one direction or another are not large enough, the mineral will not display cleavage. Corundum, for example, displays no cleavage. (Full article...)
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Micas (/ˈmaɪkəz/ MY-kəz) are a group of silicate minerals whose outstanding physical characteristic is that individual mica crystals can easily be split into fragile elastic plates. This characteristic is described as perfect basal cleavage. Mica is common in igneous and metamorphic rock and is occasionally found as small flakes in sedimentary rock. It is particularly prominent in many granites, pegmatites, and schists, and "books" (large individual crystals) of mica several feet across have been found in some pegmatites.

Micas are used in products such as drywalls, paints, and fillers, especially in parts for automobiles, roofing, and in electronics. The mineral is used in cosmetics and food to add "shimmer" or "frost". (Full article...)
$Image 18 Malachite from the Democratic Republic of the Congo Malachite is a copper carbonate hydroxide mineral, with the formula Cu2CO3(OH)2. This opaque, green-banded mineral crystallizes in the monoclinic crystal system, and most often forms botryoidal, fibrous, or stalagmitic masses, in fractures and deep, underground spaces, where the water table and hydrothermal fluids provide the means for chemical precipitation. Individual crystals are rare, but occur as slender to acicular prisms. Pseudomorphs after more tabular or blocky azurite crystals also occur. (Full article...)$

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Malachite from the Democratic Republic of the Congo

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...)
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The 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. (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...)
$Image 21 Quartz crystal cluster from Brazil Quartz is a hard, crystalline mineral composed of silica (silicon dioxide). The atoms are linked in a continuous framework of SiO4 silicon–oxygen tetrahedra, with each oxygen being shared between two tetrahedra, giving an overall chemical formula of SiO2. Quartz is, therefore, classified structurally as a framework silicate mineral and compositionally as an oxide mineral. Quartz is the second most abundant mineral in Earth's continental crust, behind feldspar. Quartz exists in two forms, the normal α-quartz and the high-temperature β-quartz, both of which are chiral. The transformation from α-quartz to β-quartz takes place abruptly at 573 °C (846 K; 1,063 °F). Since the transformation is accompanied by a significant change in volume, it can easily induce microfracturing of ceramics or rocks passing through this temperature threshold. There are many different varieties of quartz, several of which are classified as gemstones. Since antiquity, varieties of quartz have been the most commonly used minerals in the making of jewelry and hardstone carvings, especially in Europe and Asia. Quartz is the mineral defining the value of 7 on the Mohs scale of hardness, a qualitative scratch method for determining the hardness of a material to abrasion. (Full article...)$

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Quartz crystal cluster from Brazil

Quartz is a hard, crystalline mineral composed of silica (silicon dioxide). The atoms are linked in a continuous framework of SiO₄ silicon–oxygen tetrahedra, with each oxygen being shared between two tetrahedra, giving an overall chemical formula of SiO₂. Quartz is, therefore, classified structurally as a framework silicate mineral and compositionally as an oxide mineral. Quartz is the second most abundant mineral in Earth's continental crust, behind feldspar.

Quartz exists in two forms, the normal α-quartz and the high-temperature β-quartz, both of which are chiral. The transformation from α-quartz to β-quartz takes place abruptly at 573 °C (846 K; 1,063 °F). Since the transformation is accompanied by a significant change in volume, it can easily induce microfracturing of ceramics or rocks passing through this temperature threshold.

There are many different varieties of quartz, several of which are classified as gemstones. Since antiquity, varieties of quartz have been the most commonly used minerals in the making of jewelry and hardstone carvings, especially in Europe and Asia.

Quartz is the mineral defining the value of 7 on the Mohs scale of hardness, a qualitative scratch method for determining the hardness of a material to abrasion. (Full article...)
$Image 22 A rough diamond Diamond is a solid form of the element carbon with its atoms arranged in a crystal structure called diamond cubic. Diamond as a form of carbon is tasteless, odourless, strong, brittle solid, colourless in pure form, a poor conductor of electricity, and insoluble in water. Another solid form of carbon known as graphite is the chemically stable form of carbon at room temperature and pressure, but diamond is metastable and converts to it at a negligible rate under those conditions. Diamond has the highest hardness and thermal conductivity of any natural material, properties that are used in major industrial applications such as cutting and polishing tools. They are also the reason that diamond anvil cells can subject materials to pressures found deep in the Earth. Because the arrangement of atoms in diamond is extremely rigid, few types of impurity can contaminate it (two exceptions are boron and nitrogen). Small numbers of defects or impurities (about one per million of lattice atoms) can color a diamond blue (boron), yellow (nitrogen), brown (defects), green (radiation exposure), purple, pink, orange, or red. Diamond also has a very high refractive index and a relatively high optical dispersion. Most natural diamonds have ages between 1 billion and 3.5 billion years. Most were formed at depths between 150 and 250 kilometres (93 and 155 mi) in the Earth's mantle, although a few have come from as deep as 800 kilometres (500 mi). Under high pressure and temperature, carbon-containing fluids dissolved various minerals and replaced them with diamonds. Much more recently (hundreds to tens of million years ago), they were carried to the surface in volcanic eruptions and deposited in igneous rocks known as kimberlites and lamproites. Synthetic diamonds can be grown from high-purity carbon under high pressures and temperatures or from hydrocarbon gases by chemical vapor deposition (CVD). Natural and synthetic diamonds are most commonly distinguished using optical techniques or thermal conductivity measurements. (Full article...)$

Image 22

A rough diamond

Diamond is a solid form of the element carbon with its atoms arranged in a crystal structure called diamond cubic. Diamond as a form of carbon is tasteless, odourless, strong, brittle solid, colourless in pure form, a poor conductor of electricity, and insoluble in water. Another solid form of carbon known as graphite is the chemically stable form of carbon at room temperature and pressure, but diamond is metastable and converts to it at a negligible rate under those conditions. Diamond has the highest hardness and thermal conductivity of any natural material, properties that are used in major industrial applications such as cutting and polishing tools. They are also the reason that diamond anvil cells can subject materials to pressures found deep in the Earth.

Because the arrangement of atoms in diamond is extremely rigid, few types of impurity can contaminate it (two exceptions are boron and nitrogen). Small numbers of defects or impurities (about one per million of lattice atoms) can color a diamond blue (boron), yellow (nitrogen), brown (defects), green (radiation exposure), purple, pink, orange, or red. Diamond also has a very high refractive index and a relatively high optical dispersion.

Most natural diamonds have ages between 1 billion and 3.5 billion years. Most were formed at depths between 150 and 250 kilometres (93 and 155 mi) in the Earth's mantle, although a few have come from as deep as 800 kilometres (500 mi). Under high pressure and temperature, carbon-containing fluids dissolved various minerals and replaced them with diamonds. Much more recently (hundreds to tens of million years ago), they were carried to the surface in volcanic eruptions and deposited in igneous rocks known as kimberlites and lamproites.

Synthetic diamonds can be grown from high-purity carbon under high pressures and temperatures or from hydrocarbon gases by chemical vapor deposition (CVD). Natural and synthetic diamonds are most commonly distinguished using optical techniques or thermal conductivity measurements. (Full article...)
Image 23

Dolomite (white) on talc

Dolomite (/ˈdɒl.əˌmaɪt, ˈdoʊ.lə-/) is an anhydrous carbonate mineral composed of calcium magnesium carbonate, ideally CaMg(CO₃)₂. The term is also used for a sedimentary carbonate rock composed mostly of the mineral dolomite (see Dolomite (rock)). An alternative name sometimes used for the dolomitic rock type is dolostone. (Full article...)
Image 24

Apatite (CaF) (fluorapatite) doubly-terminated crystal in calcite

Apatite is a group of phosphate minerals, usually hydroxyapatite, fluorapatite and chlorapatite, with high concentrations of OH⁻, F⁻ and Cl⁻ ion, respectively, in the crystal. The formula of the admixture of the three most common endmembers is written as Ca₁₀(PO₄)₆(OH,F,Cl)₂, and the crystal unit cell formulae of the individual minerals are written as Ca₁₀(PO₄)₆(OH)₂, Ca₁₀(PO₄)₆F₂ and Ca₁₀(PO₄)₆Cl₂.

The mineral was named apatite by the German geologist Abraham Gottlob Werner in 1786, although the specific mineral he had described was reclassified as fluorapatite in 1860 by the German mineralogist Karl Friedrich August Rammelsberg. Apatite is often mistaken for other minerals. This tendency is reflected in the mineral's name, which is derived from the Greek word ἀπατάω (apatáō), which means to deceive. (Full article...)
Image 25

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.

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...)

List of selected articles

Selected mineralogist

Image 1
Georg 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 2

Franz Toula (20 December 1845 in Vienna – 3 January 1920 in Vienna) was an Austrian geologist, mineralogist and paleontologist. (Full article...)
Image 3
Harry von Eckermann, 1916

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 4
Sigmund Zois by Janez Andrej Herrlein

Sigmund Zois Freiherr von Edelstein, usually referred as Sigmund Zois (Slovene: Žiga Zois, formerly Slovenized as Cojs or Cojz; pronunciation) (23 November 1747 – 10 November 1819) was a Carniolan nobleman, natural scientist and patron of the arts. He is considered one of the most influential figures of the Enlightenment Era in the Slovene Lands of Habsburg Austria. (Full article...)
Image 5
Li Shizhen (July 3, 1518 – 1593), courtesy name Dongbi, was a Chinese acupuncturist, herbalist, naturalist, pharmacologist, physician, and writer of the Ming dynasty. He is the author of a 27-year work, the Compendium of Materia Medica (Bencao Gangmu; Chinese: 本草綱目). He developed several methods for classifying herb components and medications for treating diseases.

The Compendium is a pharmacology text with 1,892 entries, with details about more than 1,800 traditional Chinese medicines, including 1,100 illustrations and 11,000 prescriptions. It also described the type, form, flavor, nature and application in disease treatments of 1,094 herbs. The book has been translated into several languages. The treatise included various related subjects such as botany, zoology, mineralogy, and metallurgy. Five original editions still exist. (Full article...)
Image 6

René Just Haüy (French pronunciation: [aɥi]) FRS MWS FRSE (28 February 1743 – 1 June 1822) was a French priest and mineralogist, commonly styled the Abbé Haüy after he was made an honorary canon of Notre Dame. Due to his innovative work on crystal structure and his four-volume Traité de Minéralogie (1801), he is often referred to as the "Father of Modern Crystallography". During the French Revolution he also helped to establish the metric system. (Full article...)
Image 7

Friedrich Johann Karl Becke (31 December 1855, in Prague – 18 June 1931, in Vienna) was an Austrian mineralogist and petrographer. (Full article...)
Image 8

Johan Afzelius

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 9
Johann Friedrich Ludwig Hausmann

Johann Friedrich Ludwig Hausmann (22 February 1782 – 26 December 1859) was a German mineralogist. (Full article...)
Image 10

Karl Friedrich August Rammelsberg (1 April 1813 – 28 December 1899) was a German mineralogist from Berlin, Prussia. (Full article...)
Image 11
Alexander Sadebeck (26 June 1843 in Breslau – 9 December 1879 in Hamburg) was a German geologist and mineralogist. He was a brother of botanist Richard Sadebeck (1839–1905).

He studied mineralogy and geology at the University of Berlin as a pupil of Gustav Rose. In 1865 he received his doctorate with a dissertation on Upper Jurassic formations in Pomerania. In 1872 he was appointed professor of mineralogy and geology at the University of Kiel. (Full article...)
Image 12

Pencil drawing of Miers by William Rothenstein, 1917

Sir Henry Alexander Miers, FRS (25 May 1858 – 10 December 1942) was a British mineralogist and crystallographer.

Born in Rio de Janeiro, Brazil, he was educated at Eton College and Trinity College, Oxford. He was elected a Fellow of the Royal Society in 1896. (Full article...)
Image 13
Franz Ludwig von Cancrin

Franz Ludwig von Cancrin (February 21, 1738 in Breidenbach – 1812) was a German mineralogist, metallurgist, architect and writer.

He was born into a German mining family where he was trained by his father in the science of mining. In 1764, he entered the service of the landgrave of Hesse-Kassel at Hanau, becoming professor of mathematics at the military academy, head of the civil engineering department of the state, director of the theatre and (1774) of the mint. A work on the copper mines of Elesse (1767) earned him a European reputation, and in 1783 he accepted from Catherine II of Russia the directorship of the famous Staraya salt-works, living thenceforth in Russia. (Full article...)
Image 14
Sarah Mawe (1767-1846) was an English mineralogist of the 19th century, appointed to serve Queen Victoria in that capacity from 1837 to 1840. (Full article...)
Image 15
Ernest (Ernie) Henry Nickel (born Ernst Heinrich Nickel on 31 August 1925 in Louth, Ontario, died on 18 July 2009) was a mineralogist from Canada who emigrated to Australia. He is best known as an editor of the ninth edition of the Nickel-Strunz classification together with Karl Hugo Strunz. (Full article...)
Image 16
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 17
Paul Hautefeuille (ca. 1890)

Paul Gabriel Hautefeuille (2 December 1836 in Étampes – 8 December 1902 in Paris) was a French mineralogist and chemist. (Full article...)
Image 18
Douglas Saxon Coombs (23 November 1924 – 23 December 2016) was a New Zealand mineralogist and petrologist. (Full article...)
Image 19
Jens Esmark

Jens Esmark (31 January 1763 – 26 January 1839) was a Danish-Norwegian professor of mineralogy who contributed to many of the initial discoveries and conceptual analyses of glaciers, specifically the concept that glaciers had covered larger areas in the past. (Full article...)
Image 20

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...)
Image 21
Nikolai Ivanovich Koksharov

Nikolai Ivanovich Koksharov (Russian: Николай Иванович Кокшаров) (23 November (5 December), 1818 – 21 December (2 January), 1893) was a Russian mineralogist, crystallographer, and major general in the Russian army. He was noted for his measurements of crystals using a goniometer. (Full article...)
Image 22

Franz Ernst Neumann.
Portrait by Carl Steffeck (1886)

Franz Ernst Neumann (11 September 1798 – 23 May 1895) was a German mineralogist and physicist. He devised the first formulas to calculate inductance. He also formulated Neumann's law for molecular heat. In electromagnetism, he is credited for introducing the magnetic vector potential. (Full article...)
Image 23

Stipple engraving by Friedrich Wilhelm Bollinger [de], 1777–1825

Gaius Plinius Secundus (AD 23/24–79), known in English as Pliny the Elder (/ˈplɪni/ PLIN-ee), was a Roman author, naturalist, and naval and army commander of the early Roman Empire, and a friend of the emperor Vespasian. He 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 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 24

Maurice Armand Chaper (13 February 1834, Dijon – 5 July 1896, Vienna) was a French geologist and mining engineer.

He received his education at the École Polytechnique and École des Mines, afterwards working at jobs for the railroads and public works. He enlisted in the National Guard during the Franco-Prussian War, rising to the rank of lieutenant-colonel in the 38th Regiment. In 1872 he was named assistant mayor of the 5th arrondissement of Paris. (Full article...)
Image 25
Sjur Aasmundsen Sexe (14 August 1808 – 17 February 1888) was a Norwegian mineralogist and educator. (Full article...)

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General images

The following are images from various mineral-related articles on Wikipedia.

Image 1Muscovite, a mineral species in the mica group, within the phyllosilicate subclass (from Mineral)
Image 2Sphalerite crystal partially encased in calcite from the Devonian Milwaukee Formation of Wisconsin (from Mineral)
Image 3Pyrite has a metallic lustre. (from Mineral)
Image 4Crystals of serandite, natrolite, analcime, and aegirine from Mont Saint-Hilaire, Quebec, Canada (from Mineral)
Image 5Carnotite (yellow) is a radioactive uranium-bearing mineral. (from Mineral)
Image 6Pyrite (from Lustre (mineralogy))
Image 7Perfect basal cleavage as seen in biotite (black), and good cleavage seen in the matrix (pink orthoclase). (from Mineral)
Image 8Pink 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 9Aegirine, an iron-sodium clinopyroxene, is part of the inosilicate subclass. (from Mineral)
Image 10Red cinnabar (HgS), a mercury ore, on dolomite. (from Mineral)
Image 11Gypsum desert rose (from Mineral)
Image 12Native 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 13Black andradite, an end-member of the orthosilicate garnet group. (from Mineral)
Image 14Natrolite is a mineral series in the zeolite group; this sample has a very prominent acicular crystal habit. (from Mineral)
Image 15Mohs Scale versus Absolute Hardness (from Mineral)
Image 16Epidote often has a distinctive pistachio-green colour. (from Mineral)
Image 17Contact twins, as seen in spinel (from Mineral)
Image 18Mohs hardness kit, containing one specimen of each mineral on the ten-point hardness scale (from Mohs scale)
Image 19An example of elbaite, a species of tourmaline, with distinctive colour banding. (from Mineral)
Image 20Topaz has a characteristic orthorhombic elongated crystal shape. (from Mineral)
Image 21Hübnerite, the manganese-rich end-member of the wolframite series, with minor quartz in the background (from Mineral)
Image 22Diamond is the hardest natural material, and has a Mohs hardness of 10. (from Mineral)
Image 23Galena, PbS, is a mineral with a high specific gravity. (from Mineral)
Image 24Schist is a metamorphic rock characterized by an abundance of platy minerals. In this example, the rock has prominent sillimanite porphyroblasts as large as 3 cm (1.2 in). (from Mineral)
Image 25Asbestiform tremolite, part of the amphibole group in the inosilicate subclass (from Mineral)
Image 26When 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)

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?

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v t e Minerals
Overview	Mineral Mineralogy History of mineralogy
Common minerals	Amphibole Bridgmanite K-feldspar Mica Olivine Plagioclase Pyroxene Quartz Spinel

v t e Phosphate minerals
Crystalline	Allanpringite Beraunite Brazilianite Eosphorite Fluorapatite Hydroxyapatite Lithiophilite Metatorbernite Monazite Struvite Taranakite Variscite Wavellite Xenotime
Cryptocrystalline	Turquoise Whitlockite
Amorphous	Santabarbaraite Scorodite

v t e Phyllosilicates
Micas	Aluminoceladonite Anandite Annite Aspidolite Balestraite Bityite Biotite Boromuscovite Bramallite Celadonite Chernykhite Chromphyllite Clintonite Eastonite Ephesite Ferroaluminoceladonite Ferroceladonite Fluorannite Fluorokinoshitalite Fluorophlogopite Fluorotetraferriphlogopite Garmite Glauconite Gorbunovite Hendricksite Illite Kinoshitalite Lepidolite Luanshiweiite Manganiceladonite Margarite Masutomilite Montdorite Muscovite Nanpingite Norrishite Orlovite Oxyphlogopite Paragonite Phlogopite Polylithionite Preiswerkite Roscoelite Siderophyllite Suhailite Tainiolite Tetraferriannite Trilithionite Voloshinite Wonesite Yangzhumingite
Talcs	Minnesotaite Talc Willemseite
Pyrophyllite series	Ferripyrophyllite Pyrophyllite
Kaolinites	Bismutoferrite Dickite Halloysite Hisingerite Kaolinite Nacrite
Serpentines	Amesite Antigorite Berthierine Brindleyite Caryopilite Chrysotile Cronstedtite Fraipontite Greenalite Guidottiite Kellyite Lizardite Manandonite Népouite Odinite Pecoraite
Corrensites	Aliettite Brinrobertsite Corrensite Dozyite Hydrobiotite Karpinskite Kulkeite Lunijianlaite Rectorite Saliotite Tosudite
Smectites and vermiculite family	Beidellite Ferrosaponite Montmorillonite Nontronite Saponite Sauconite Swinefordite Vermiculite Volkonskoite Yakhontovite
Chlorites	Baileychlore Borocookeite Chamosite Clinochlore Cookeite Donbassite Gonyerite Nimite Pennantite Sudoite
Allophanes	Allophane Chrysocolla Imogolite Neotocite
Sepiolites	Falcondoite Ferrisepiolite Sepiolite
Pyrosmalites	Friedelite Mcgillite Nelenite Pyrosmalite Schallerite
Stilpnomelanes	Bannisterite Franklinphilite Lennilenapeite Parsettensite Stilpnomelane
Structural groups mainly; based on rruff.info/ima, modified

v t e IMA–CNMNC / Nickel–Strunz IDs Mineral categories (classes, subclasses, divisions)
"Special cases" ("native elements and organic minerals")	"Native elements" (IDs 1) Organic minerals (IDs 10)
"Sulfides and oxides"	Sulfides (IDs 2.A–F) Sulfosalts; sulfarsenites, sulfantimonites, sulfbismuthites (IDs 2.G) Sulfosalts; sulfarsenates, sulfantimonates (IDs 2.K) Other sulfosalts (IDs 2.H–J and 2.L–M) Oxides (IDs 4.A–E, e.g. pyrochlore supergroup and corundum group) Hydroxides (IDs 4.F–G) Arsenates(IV), sulfates(IV) and iodates (IDs 4.J–K) Tellurium oxysalts Vanadium oxides (IDs 4.H)
"Evaporites and similars"	Carbonates (IDs 5.A–E) Nitrates (IDs 5.N) Borates (IDs 6) Halides (IDs 3)
"Mineral structures with tetrahedral units" (sulfate anion, phosphate anion, silicon, etc.)	Monomeric minerals (similar to nesosilicates) Sulfates(VI) (IDs 7.A–E) Thiosulphates (IDs 7.J) Chromates(VI) (IDs 7.F) Molybdates, wolframates, niobates(VI) (IDs 7.G–H) Phosphates(V) (IDs 8) Arsenates, vanadates(V) (IDs 8) Monomeric, isolated silicates (IDs 9.A) Germanates (IDs 9.J) Silicate frameworks, tectosilicates Zeolite frameworks, zeolite family (IDs 9.G) Other feldspathoids: nephelines (IDs 9.FA.05) Cancrinite-sodalite groups (IDs 9.FB.) Other tectosilicates (IDs 9.FA. and 9.FB.15, e.g. feldspars) Other silicate frameworks Cyclosilicates (IDs 9.C) Phyllosilicates (IDs 9.E, e.g. clays) Silica family (IDs 4.DA.) Inosilicates Single chain inosilicates (IDs 9.D, e.g. pyroxenes) Ribbon or multiple chain inosilicates (IDs 9.D, e.g. amphiboles) Other non monomeric minerals Unclassified silicates (IDs 9.H) Sorosilicates (IDs 9.B, e.g. epidote and seidozerite supergroups) Polymeric, isolated silicates (IDs 9.A, e.g. olivine and gadolinite supergroups) Other inorganic polymers (e.g. polyoxometalates; "polyphosphates", IDs 8.F)