1.
Jequitinhonha River
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The Jequitinhonha River flows mainly through the Brazilian state of Minas Gerais. Its source lies near Diamantina in the Espinhaço Mountains at an elevation of 1,200 metres, after which it flows northward, at Salto da Divisa, it is interrupted by the Cachoeira do Salto Grande,43 metres high. The main tributaries are the Araçuaí River, Piauí, São Miguel, Itacambiruçu, Salinas, São Pedro, the valley of the Jequitinhonha is one of the poorest regions of Brazil and is still prone to endemic yellow fever. It covers 78,451 square kilometres, twice the size of Switzerland, the most populous of these is Almenara located on the middle Jequitinhonha. The valley is known for its variety of gemstones, colonial-era towns, unique handicrafts, most of the soil is arid and is periodically affected by drought or floods. The economically active population numbers over 400,000, of which 180,000 are in the rural areas practicing rudimentary agriculture, industry employs 50,000 people and is the most important economic source for the municipalities. In the past the region was covered by forests and occupied by indigenous people, what contributed to the deforestation and subsequent degradation of the region was the predatory activity of mining and extraction of diamonds. Today there are attempts to develop the work of local artisans, while living in total isolation, they have developed ceramic craftwork that is mainly performed by the women, who belong to associations. They make utilitarian pieces that are ranked as the most creative works of Brazilian popular art, the famous dolls from that region are in fact pitchers for holding fresh water, thus losing this function and becoming decorative objects. The electrical company of Minas Gerais constructed a plant on the river between Berilo and Grão Mogol. The Usina Presidente Juscilino Kubitscheck, the plant powered by Irapé Dam, has an installed capacity of 360 MW. CEMIG began the work in 2002 and in April 2003 diverted the river to two tunnels with a length of more than 1.2 km, the dam and power station were completed in 2006. List of rivers of Bahia Photos of the Jequitinhonha Map of Doce and Jequitinhonha Rivers Copied from Documents Found in the House of Representatives from the 19th century
2.
Minas Gerais
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Minas Gerais is a state in the north of Southeastern Brazil. It ranks as the second most populous, the third by gross domestic product, Minas Gerais is the state with the largest number of Brazilian presidents. With an area of 586,528 square kilometres —larger than Metropolitan France—it is the fourth most extensive state in Brazil. In the south, the tourist points are the mineral spas, such as Caxambu, Lambari, São Lourenço, Poços de Caldas, São Thomé das Letras, Monte Verde. The landscape of the State is marked by mountains, valleys, in the Serra do Cipó, Sete Lagoas, Cordisburgo and Lagoa Santa, the caves and waterfalls are the attractions. Some of Brazils most famous caverns are located there, in recent years, the state has emerged as one of the largest economic forces of Brazil, exploring its great economic potential. Two interpretations are given for the origin of the name Minas Gerais and it comes from Minas dos Matos Gerais, the former name of the colonial province. Another explanation is that this ignores the two large geographical spaces which conformed the state in its history, the region of the mines, and these corresponded to the areas of Sertão which were farther and hard to access from the mining spots. The confusion comes from the fact that the term Gerais is taken as an adjective to Minas in the first version, Minas Gerais is in the north of the southeastern subdivision of Brasil, which also contains the states of São Paulo, Rio de Janeiro and Espírito Santo. It borders on Bahia, Goiás, Mato Grosso do Sul, the states of São Paulo and Rio de Janeiro and it also shares a short boundary with the Distrito Federal. Minas Gerais is situated between 14°1358 and 22°5400 S latitude and between 39°5132 and 51°0235 W longitude and it is larger in area than Metropolitan France or Spain. Minas Gerais features some of the longest rivers in Brazil, most notably the São Francisco, the Paraná and to a lesser extent, the state also holds many hydroelectric power plants, including Furnas. The most notable one is the Pico da Bandeira, the third highest mountain in Brazil at 2890 m, the state also has huge reserves of iron and sizeable reserves of gold and gemstones, including emerald, topaz and aquamarine mines. Emeralds found in location are comparable to the best Colombia-origin emeralds. Each region of the state has a character, geographically. The central and eastern area of the state is hilly and rocky, around Lagoa Santa and Sete Lagoas a typical Karst topography with caves and lakes is found. Some of the mountains are almost entirely iron ore, which led to extensive mining, recent advances in environmental policy helped to put limits to mining. Vale do Aços largest cities are Ipatinga, Coronel Fabriciano and Timóteo, now that mining is restricted large areas of forest are being removed for timber, charcoal and to clear land for cattle ranching
3.
Tectosilicate
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Silicate minerals are rock-forming minerals made up of silicate groups. They are the largest and most important class of rock-forming minerals and they are classified based on the structure of their silicate groups, which contain different ratios of silicon and oxygen. Nesosilicates, or orthosilicates, have the orthosilicate ion, which constitute isolated 4− tetrahedra that are connected only by interstitial cations and these exist as 3-member 6− and 6-member 12− rings, where T stands for a tetrahedrally coordinated cation. Inosilicates, or chain silicates, have interlocking chains of silicate tetrahedra with either SiO3,1,3 ratio, for single chains or Si4O11,4,11 ratio, for double chains. Nickel–Strunz classification,09. D Pyroxene group Enstatite – orthoferrosilite series Enstatite – MgSiO3 Ferrosilite – FeSiO3 Pigeonite – Ca0.251, all phyllosilicate minerals are hydrated, with either water or hydroxyl groups attached. Serpentine subgroup Antigorite – Mg3Si2O54 Chrysotile – Mg3Si2O54 Lizardite – Mg3Si2O54 Clay minerals group Halloysite – Al2Si2O54 Kaolinite – Al2Si2O54 Illite – 24O10 Montmorillonite –0 and this group comprises nearly 75% of the crust of the Earth. Tectosilicates, with the exception of the group, are aluminosilicates. Nickel–Strunz classification,09. F and 09. G,04. A, an introduction to the rock-forming minerals. Wise, W. S. Zussman, J. Rock-forming minerals, P.982 pp. Hurlbut, Cornelius S. Danas Manual of Mineralogy. Mindat. org, Dana classification Webmineral, Danas New Silicate Classification Media related to Silicates at Wikimedia Commons
4.
Chemical formula
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These are limited to a single typographic line of symbols, which may include subscripts and superscripts. A chemical formula is not a name, and it contains no words. Although a chemical formula may imply certain simple chemical structures, it is not the same as a full chemical structural formula. Chemical formulas can fully specify the structure of only the simplest of molecules and chemical substances, the simplest types of chemical formulas are called empirical formulas, which use letters and numbers indicating the numerical proportions of atoms of each type. Molecular formulas indicate the numbers of each type of atom in a molecule. For example, the formula for glucose is CH2O, while its molecular formula is C6H12O6. This is possible if the relevant bonding is easy to show in one dimension, an example is the condensed molecular/chemical formula for ethanol, which is CH3-CH2-OH or CH3CH2OH. For reasons of structural complexity, there is no condensed chemical formula that specifies glucose, chemical formulas may be used in chemical equations to describe chemical reactions and other chemical transformations, such as the dissolving of ionic compounds into solution. A chemical formula identifies each constituent element by its chemical symbol, in empirical formulas, these proportions begin with a key element and then assign numbers of atoms of the other elements in the compound, as ratios to the key element. For molecular compounds, these numbers can all be expressed as whole numbers. For example, the formula of ethanol may be written C2H6O because the molecules of ethanol all contain two carbon atoms, six hydrogen atoms, and one oxygen atom. Some types of compounds, however, cannot be written with entirely whole-number empirical formulas. An example is boron carbide, whose formula of CBn is a variable non-whole number ratio with n ranging from over 4 to more than 6.5. When the chemical compound of the consists of simple molecules. These types of formulas are known as molecular formulas and condensed formulas. A molecular formula enumerates the number of atoms to reflect those in the molecule, so that the formula for glucose is C6H12O6 rather than the glucose empirical formula. However, except for very simple substances, molecular chemical formulas lack needed structural information, for simple molecules, a condensed formula is a type of chemical formula that may fully imply a correct structural formula. For example, ethanol may be represented by the chemical formula CH3CH2OH
5.
Potassium
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Potassium is a chemical element with symbol K and atomic number 19. It was first isolated from potash, the ashes of plants, in the periodic table, potassium is one of the alkali metals. Potassium in nature only in ionic salts. It is found dissolved in sea water, and is part of many minerals, naturally occurring potassium is composed of three isotopes, of which 40K is radioactive. Traces of 40K are found in all potassium, and it is the most common radioisotope in the human body, Potassium is chemically very similar to sodium, the previous element in Group 1 of the periodic table. They have a similar energy, which allows for each atom to give up its sole outer electron. That they are different elements combine with the same anions to make similar salts was suspected in 1702. Most industrial applications of potassium exploit the high solubility in water of potassium compounds, heavy crop production rapidly depletes the soil of potassium, and this can be remedied with agricultural fertilizers containing potassium, accounting for 95% of global potassium chemical production. Potassium ions are necessary for the function of all living cells, fresh fruits and vegetables are good dietary sources of potassium. Potassium is the second least dense metal after lithium and it is a soft solid with a low melting point, and can be easily cut with a knife. Freshly cut potassium is silvery in appearance, but it begins to tarnish toward gray immediately on exposure to air, in a flame test, potassium and its compounds emit a lilac color with a peak emission wavelength of 766.5 nanometers. Neutral potassium atoms have 19 electrons, one more than the stable configuration of the noble gas argon. This process requires so little energy that potassium is readily oxidized by atmospheric oxygen, in contrast, the second ionization energy is very high, because removal of two electrons breaks the stable noble gas electronic configuration. Potassium therefore does not readily form compounds with the state of +2 or higher. Potassium is an active metal that reacts violently with oxygen in water. With oxygen it forms potassium peroxide, and with water potassium forms potassium hydroxide, the reaction of potassium with water is dangerous because of its violent exothermic character and the production of hydrogen gas. Hydrogen reacts again with atmospheric oxygen, producing water, which reacts with the remaining potassium and this reaction requires only traces of water, because of this, potassium and the liquid sodium-potassium — NaK — are potent desiccants that can be used to dry solvents prior to distillation. Because of the sensitivity of potassium to water and air, reactions with other elements are only in an inert atmosphere such as argon gas using air-free techniques
6.
Aluminium
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Aluminium or aluminum is a chemical element in the boron group with symbol Al and atomic number 13. It is a silvery-white, soft, nonmagnetic, ductile metal, Aluminium metal is so chemically reactive that native specimens are rare and limited to extreme reducing environments. Instead, it is combined in over 270 different minerals. The chief ore of aluminium is bauxite, Aluminium is remarkable for the metals low density and its ability to resist corrosion through the phenomenon of passivation. Aluminium and its alloys are vital to the industry and important in transportation and structures, such as building facades. The oxides and sulfates are the most useful compounds of aluminium, despite its prevalence in the environment, no known form of life uses aluminium salts metabolically, but aluminium is well tolerated by plants and animals. Because of these salts abundance, the potential for a role for them is of continuing interest. Aluminium is a soft, durable, lightweight, ductile. It is nonmagnetic and does not easily ignite, a fresh film of aluminium serves as a good reflector of visible light and an excellent reflector of medium and far infrared radiation. The yield strength of aluminium is 7–11 MPa, while aluminium alloys have yield strengths ranging from 200 MPa to 600 MPa. Aluminium has about one-third the density and stiffness of steel and it is easily machined, cast, drawn and extruded. Aluminium atoms are arranged in a cubic structure. Aluminium has an energy of approximately 200 mJ/m2. Aluminium is a thermal and electrical conductor, having 59% the conductivity of copper. Aluminium is capable of superconductivity, with a critical temperature of 1.2 kelvin. Aluminium is the most common material for the fabrication of superconducting qubits, the strongest aluminium alloys are less corrosion resistant due to galvanic reactions with alloyed copper. This corrosion resistance is reduced by aqueous salts, particularly in the presence of dissimilar metals. In highly acidic solutions, aluminium reacts with water to form hydrogen, primarily because it is corroded by dissolved chlorides, such as common sodium chloride, household plumbing is never made from aluminium
7.
Silicon
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Silicon is a chemical element with symbol Si and atomic number 14. A hard and brittle crystalline solid with a metallic luster. It is a member of group 14 in the table, along with carbon above it and germanium, tin, lead. It is not very reactive, although more reactive than germanium, Silicon is the eighth most common element in the universe by mass, but very rarely occurs as the pure element in the Earths crust. It is most widely distributed in dusts, sands, planetoids, over 90% of the Earths crust is composed of silicate minerals, making silicon the second most abundant element in the Earths crust after oxygen. Most silicon is used commercially without being separated, and often with little processing of the natural minerals, such use includes industrial construction with clays, silica sand, and stone. Silicate is used in Portland cement for mortar and stucco, and mixed with sand and gravel to make concrete for walkways, foundations. Silicates are used in whiteware ceramics such as porcelain, and in traditional quartz-based soda-lime glass, Silicon compounds such as silicon carbide are used as abrasives and components of high-strength ceramics. Elemental silicon also has an impact on the modern world economy. Most free silicon is used in the refining, aluminium-casting. Silicon is the basis of the widely used synthetic polymers called silicones, Silicon is an essential element in biology, although only tiny traces are required by animals. However, various sea sponges and microorganisms, such as diatoms and radiolaria, silica is deposited in many plant tissues, such as in the bark and wood of Chrysobalanaceae and the silica cells and silicified trichomes of Cannabis sativa, horsetails and many grasses. Silicon is a solid at room temperature, with a point of 1,414 °C. Like water, it has a density in a liquid state than in a solid state and it expands when it freezes. With a relatively high conductivity of 149 W·m−1·K−1, silicon conducts heat well. In its crystalline form, pure silicon has a gray color, like germanium, silicon is rather strong, very brittle, and prone to chipping. Silicon, like carbon and germanium, crystallizes in a cubic crystal structure with a lattice spacing of 0.5430710 nm. The outer electron orbital of silicon, like that of carbon, has four valence electrons, the 1s, 2s, 2p and 3s subshells are completely filled while the 3p subshell contains two electrons out of a possible six
8.
Oxygen
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Oxygen is a chemical element with symbol O and atomic number 8. It is a member of the group on the periodic table and is a highly reactive nonmetal. By mass, oxygen is the third-most abundant element in the universe, after hydrogen, at standard temperature and pressure, two atoms of the element bind to form dioxygen, a colorless and odorless diatomic gas with the formula O2. This is an important part of the atmosphere and diatomic oxygen gas constitutes 20. 8% of the Earths atmosphere, additionally, as oxides the element makes up almost half of the Earths crust. Most of the mass of living organisms is oxygen as a component of water, conversely, oxygen is continuously replenished by photosynthesis, which uses the energy of sunlight to produce oxygen from water and carbon dioxide. Oxygen is too reactive to remain a free element in air without being continuously replenished by the photosynthetic action of living organisms. Another form of oxygen, ozone, strongly absorbs ultraviolet UVB radiation, but ozone is a pollutant near the surface where it is a by-product of smog. At low earth orbit altitudes, sufficient atomic oxygen is present to cause corrosion of spacecraft, the name oxygen was coined in 1777 by Antoine Lavoisier, whose experiments with oxygen helped to discredit the then-popular phlogiston theory of combustion and corrosion. One of the first known experiments on the relationship between combustion and air was conducted by the 2nd century BCE Greek writer on mechanics, Philo of Byzantium. In his work Pneumatica, Philo observed that inverting a vessel over a burning candle, Philo incorrectly surmised that parts of the air in the vessel were converted into the classical element fire and thus were able to escape through pores in the glass. Many centuries later Leonardo da Vinci built on Philos work by observing that a portion of air is consumed during combustion and respiration, Oxygen was discovered by the Polish alchemist Sendivogius, who considered it the philosophers stone. In the late 17th century, Robert Boyle proved that air is necessary for combustion, English chemist John Mayow refined this work by showing that fire requires only a part of air that he called spiritus nitroaereus. From this he surmised that nitroaereus is consumed in both respiration and combustion, Mayow observed that antimony increased in weight when heated, and inferred that the nitroaereus must have combined with it. Accounts of these and other experiments and ideas were published in 1668 in his work Tractatus duo in the tract De respiratione. Robert Hooke, Ole Borch, Mikhail Lomonosov, and Pierre Bayen all produced oxygen in experiments in the 17th and the 18th century but none of them recognized it as a chemical element. This may have been in part due to the prevalence of the philosophy of combustion and corrosion called the phlogiston theory, which was then the favored explanation of those processes. Established in 1667 by the German alchemist J. J. Becher, one part, called phlogiston, was given off when the substance containing it was burned, while the dephlogisticated part was thought to be its true form, or calx. The fact that a substance like wood gains overall weight in burning was hidden by the buoyancy of the combustion products
9.
Sodium
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Sodium is a chemical element with symbol Na and atomic number 11. It is a soft, silvery-white, highly reactive metal, Sodium is an alkali metal, being in group 1 of the periodic table, because it has a single electron in its outer shell that it readily donates, creating a positively charged atom—the Na+ cation. Its only stable isotope is 23Na, the free metal does not occur in nature, but must be prepared from compounds. Sodium is the sixth most abundant element in the Earths crust, Sodium was first isolated by Humphry Davy in 1807 by the electrolysis of sodium hydroxide. Among many other useful compounds, sodium hydroxide is used in soap manufacture, and sodium chloride is a de-icing agent. Sodium is an element for all animals and some plants. Sodium ions are the major cation in the fluid and as such are the major contributor to the ECF osmotic pressure. Loss of water from the ECF compartment increases the sodium concentration, isotonic loss of water and sodium from the ECF compartment decreases the size of that compartment in a condition called ECF hypovolemia. In nerve cells, the charge across the cell membrane enables transmission of the nerve impulse—an action potential—when the charge is dissipated. The melting and boiling points of sodium are lower than those of lithium but higher than those of the alkali metals potassium, rubidium. All of these high-pressure allotropes are insulators and electrides.3 nm, spin-orbit interactions involving the electron in the 3p orbital split the D line into two, at 589.0 and 589.6 nm, hyperfine structures involving both orbitals cause many more lines. Twenty isotopes of sodium are known, but only 23Na is stable, 23Na is created in the carbon-burning process in stars by fusing two carbon atoms together, this requires temperatures above 600 megakelvins and a star of at least three solar masses. Two nuclear isomers have been discovered, the one being 24mNa with a half-life of around 20.2 milliseconds. Sodium atoms have 11 electrons, one more than the stable configuration of the noble gas neon. This process requires so little energy that sodium is oxidized by giving up its 11th electron. In contrast, the ionization energy is very high, because the 10th electron is closer to the nucleus than the 11th electron. As a result, sodium usually forms ionic compounds involving the Na+ cation, the most common oxidation state for sodium is +1. It is generally less reactive than potassium and more reactive than lithium, Sodium metal is highly reducing, with the reduction of sodium ions requiring −2.71 volts, though potassium and lithium have even more negative potentials
10.
Calcium
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Calcium is a chemical element with symbol Ca and atomic number 20. Calcium is a soft grayish-yellow alkaline earth metal, fifth-most-abundant element by mass in the Earths crust, the ion Ca2+ is also the fifth-most-abundant dissolved ion in seawater by both molarity and mass, after sodium, chloride, magnesium, and sulfate. Free calcium metal is too reactive to occur in nature, Calcium is produced in supernova nucleosynthesis. Calcium is a trace element in living organisms. It is the most abundant metal by mass in animals, and it is an important constituent of bone, teeth. In cell biology, the movement of the calcium ion into, Calcium carbonate and calcium citrate are often taken as dietary supplements. Calcium is on the World Health Organizations List of Essential Medicines, Calcium has a wide variety of applications, almost all of which are associated with calcium compounds and salts. Calcium metal is used as a deoxidizer, desulfurizer, and decarbonizer for production of ferrous and nonferrous alloys. In steelmaking and production of iron, Ca reacts with oxygen, Calcium carbonate is used in manufacturing cement and mortar, lime, limestone and aids in production in the glass industry. It also has chemical and optical uses as mineral specimens in toothpastes, Calcium hydroxide solution is used to detect the presence of carbon dioxide in a gas sample bubbled through a solution. The solution turns cloudy where CO2 is present, Calcium arsenate is used in insecticides. Calcium carbide is used to make acetylene gas and various plastics, Calcium chloride is used in ice removal and dust control on dirt roads, as a conditioner for concrete, as an additive in canned tomatoes, and to provide body for automobile tires. Calcium citrate is used as a food preservative, Calcium cyclamate is used as a sweetening agent in several countries. In the United States, it has been outlawed as a suspected carcinogen, Calcium gluconate is used as a food additive and in vitamin pills. Calcium hypochlorite is used as a swimming pool disinfectant, as an agent, as an ingredient in deodorant. Calcium permanganate is used in rocket propellant, textile production, as a water sterilizing agent. Calcium phosphate is used as a supplement for animal feed, fertilizer, in production for dough and yeast products, in the manufacture of glass. Calcium phosphide is used in fireworks, rodenticide, torpedoes, Calcium sulfate is used as common blackboard chalk, as well as, in its hemihydrate form, Plaster of Paris
11.
Crystal system
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In crystallography, the terms crystal system, crystal family and lattice system each refer to one of several classes of space groups, lattices, point groups or crystals. Informally, two crystals are in the crystal system if they have similar symmetries, though there are many exceptions to this. Space groups and crystals are divided into seven crystal systems according to their point groups, five of the crystal systems are essentially the same as five of the lattice systems, but the hexagonal and trigonal crystal systems differ from the hexagonal and rhombohedral lattice systems. The six crystal families are formed by combining the hexagonal and trigonal crystal systems into one hexagonal family, a lattice system is a class of lattices with the same set of lattice point groups, which are subgroups of the arithmetic crystal classes. The 14 Bravais lattices are grouped into seven lattice systems, triclinic, monoclinic, orthorhombic, tetragonal, rhombohedral, hexagonal, in a crystal system, a set of point groups and their corresponding space groups are assigned to a lattice system. Of the 32 point groups that exist in three dimensions, most are assigned to only one system, in which case both the crystal and lattice systems have the same name. However, five point groups are assigned to two systems, rhombohedral and hexagonal, because both exhibit threefold rotational symmetry. These point groups are assigned to the crystal system. In total there are seven crystal systems, triclinic, monoclinic, orthorhombic, tetragonal, trigonal, hexagonal, a crystal family is determined by lattices and point groups. It is formed by combining crystal systems which have space groups assigned to a lattice system. In three dimensions, the families and systems are identical, except the hexagonal and trigonal crystal systems. In total there are six families, triclinic, monoclinic, orthorhombic, tetragonal, hexagonal. Spaces with less than three dimensions have the number of crystal systems, crystal families and lattice systems. In one-dimensional space, there is one crystal system, in 2D space, there are four crystal systems, oblique, rectangular, square and hexagonal. The relation between three-dimensional crystal families, crystal systems and lattice systems is shown in the table, Note. To avoid confusion of terminology, the term trigonal lattice is not used, if the original structure and inverted structure are identical, then the structure is centrosymmetric. Still, even for non-centrosymmetric case, inverted structure in some cases can be rotated to align with the original structure and this is the case of non-centrosymmetric achiral structure. If the inverted structure cannot be rotated to align with the structure, then the structure is chiral
12.
Triclinic crystal system
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In crystallography, the triclinic crystal system is one of the 7 crystal systems. A crystal system is described by three basis vectors, in the triclinic system, the crystal is described by vectors of unequal length, as in the orthorhombic system. In addition, no vector is at right angles orthogonal to another, the triclinic lattice is the least symmetric of the 14 three-dimensional Bravais lattices. It is the lattice type that itself has no mirror planes. There are a total 2 space groups, with each only one space group is associated. Pinacoidal is also known as triclinic normal, pedial is also triclinic hemihedral Mineral examples include plagioclase, microcline, rhodonite, turquoise, wollastonite and amblygonite, all in triclinic normal. Crystal structure Hurlbut, Cornelius S. Klein, Cornelis,1985, Manual of Mineralogy, 20th ed. pp.64 –65, ISBN 0-471-80580-7
13.
Monoclinic crystal system
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In crystallography, the monoclinic crystal system is one of the 7 crystal systems. A crystal system is described by three vectors, in the monoclinic system, the crystal is described by vectors of unequal lengths, as in the orthorhombic system. They form a rectangular prism with a parallelogram as its base, hence two vectors are perpendicular, while the third vector meets the other two at an angle other than 90°. There is only one monoclinic Bravais lattice in two dimensions, the oblique lattice, two monoclinic Bravais lattices exist, the primitive monoclinic and the centered monoclinic lattices. In this axis setting, the primitive and base-centered lattices interchange in centering type, sphenoidal is also monoclinic hemimorphic, Domatic is also monoclinic hemihedral, Prismatic is also monoclinic normal. Crystal structure Hurlbut, Cornelius S. Klein, Cornelis, hahn, Theo, ed. International Tables for Crystallography, Volume A, Space Group Symmetry
14.
Cleavage (crystal)
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Cleavage, in mineralogy, is the tendency of crystalline materials to split along definite crystallographic structural planes. Cleavage forms parallel to planes, Basal or pinacoidal cleavage occurs when there is only one cleavage plane. Mica also has basal cleavage, this is why mica can be peeled into thin sheets, cubic cleavage occurs on when there are three cleavage planes intersecting at 90 degrees. Halite has cubic cleavage, and therefore, when halite crystals are broken, octahedral cleavage occurs when there are four cleavage planes in a crystal. Octahedral cleavage is common for semiconductors, rhombohedral cleavage occurs when there are three cleavage planes intersecting at angles that are not 90 degrees. Prismatic cleavage occurs when there are two planes in a crystal. Dodecahedral cleavage occurs when there are six cleavage planes in a crystal, crystal parting occurs when minerals break along planes of structural weakness due to external stress or along twin composition planes. Parting breaks are very similar in appearance to cleavage, but only due to stress. Examples include magnetite which shows octahedral parting, the parting of corundum. Cleavage is a property traditionally used in mineral identification, both in hand specimen and microscopic examination of rock and mineral studies. As an example, the angles between the cleavage planes for the pyroxenes and the amphiboles are diagnostic. Crystal cleavage is of importance in the electronics industry and in the cutting of gemstones. Precious stones are generally cleaved by impact, as in diamond cutting, synthetic single crystals of semiconductor materials are generally sold as thin wafers which are much easier to cleave. Elemental semiconductors are diamond cubic, a group for which octahedral cleavage is observed. This means that some orientations of wafer allow near-perfect rectangles to be cleaved, most other commercial semiconductors can be made in the related zinc blende structure, with similar cleavage planes. Cleavage Mineral galleries, Mineral properties – Cleavage
15.
Fracture (mineralogy)
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In the field of mineralogy, fracture is the texture and shape of a rocks surface formed when a mineral is fractured. Minerals often have a highly distinctive fracture, making it a feature used in their identification. Fracture differs from cleavage in that the latter involves clean splitting along the planes of the minerals crystal structure. All minerals exhibit fracture, but when very strong cleavage is present, conchoidal fracture breakage that resembles the concentric ripples of a mussel shell. It often occurs in amorphous or fine-grained minerals such as flint, opal or obsidian, subconchoidal fracture is similar to conchoidal fracture, but with less significant curvature. Earthy fracture is reminiscent of freshly broken soil and it is frequently seen in relatively soft, loosely bound minerals, such as limonite, kaolinite and aluminite. Hackly fracture is jagged, sharp and not even and it occurs when metals are torn, and so is often encountered in native metals such as copper and silver. Splintery fracture comprises sharp elongated points and it is particularly seen in fibrous minerals such as chrysotile, but may also occur in non-fibrous minerals such as kyanite. Uneven fracture is a surface or one with random irregularities. It occurs in a range of minerals including arsenopyrite, pyrite and magnetite. Rudolf Duda and Lubos Rejl, Minerals of the World http, //www. galleries. com/minerals/property/fracture. htm
16.
Mohs scale of mineral hardness
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The Mohs scale of mineral hardness is a qualitative ordinal scale characterizing scratch resistance of various minerals through the ability of harder material to scratch softer material. Created in 1812 by German geologist and mineralogist Friedrich Mohs, it is one of several definitions of hardness in materials science, while greatly facilitating the identification of minerals in the field, the Mohs scale does not show how well hard materials perform in an industrial setting. Despite its lack of precision, the Mohs scale is highly relevant for field geologists, the Mohs scale hardness of minerals can be commonly found in reference sheets. Reference materials may be expected to have a uniform Mohs hardness, the Mohs scale of mineral hardness is based on the ability of one natural sample of mineral to scratch another mineral visibly. The samples of matter used by Mohs are all different minerals, Minerals are pure substances found in nature. Rocks are made up of one or more minerals, as the hardest known naturally occurring substance when the scale was designed, diamonds are at the top of the scale. The hardness of a material is measured against the scale by finding the hardest material that the material can scratch. For example, if material is scratched by apatite but not by fluorite. Scratching a material for the purposes of the Mohs scale means creating non-elastic dislocations visible to the naked eye, frequently, materials that are lower on the Mohs scale can create microscopic, non-elastic dislocations on materials that have a higher Mohs number. The Mohs scale is an ordinal scale. For example, corundum is twice as hard as topaz, the table below shows the comparison with the absolute hardness measured by a sclerometer, with pictorial examples. On the Mohs scale, a streak plate has a hardness of 7.0, using these ordinary materials of known hardness can be a simple way to approximate the position of a mineral on the scale. The table below incorporates additional substances that may fall between levels, Comparison between Hardness and Hardness, Mohs hardness of elements is taken from G. V, samsonov in Handbook of the physicochemical properties of the elements, IFI-Plenum, New York, USA,1968. The Hardness of Minerals and Rocks
17.
Lustre (mineralogy)
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Lustre or luster is the way light interacts with the surface of a crystal, rock, or mineral. The word traces its origins back to the latin lux, meaning light, a range of terms are used to describe lustre, such as earthy, metallic, greasy, and silky. Similarly, the term refers to a glassy lustre. A list of terms is given below. Lustre varies over a continuum, and so there are no rigid boundaries between the different types of lustre. The terms are frequently combined to describe types of lustre. Some minerals exhibit unusual optical phenomena, such as asterism or chatoyancy, a list of such phenomena is given below. Adamantine minerals possess a superlative lustre, which is most notably seen in diamond, such minerals are transparent or translucent, and have a high refractive index. Minerals with an adamantine lustre are uncommon, with examples being cerussite. Minerals with a degree of lustre are referred to as subadamantine, with some examples being garnet. Dull minerals exhibit little to no lustre, due to coarse granulations which scatter light in all directions, a distinction is sometimes drawn between dull minerals and earthy minerals, with the latter being coarser, and having even less lustre. Greasy minerals resemble fat or grease, a greasy lustre often occurs in minerals containing a great abundance of microscopic inclusions, with examples including opal and cordierite. Many minerals with a greasy lustre also feel greasy to the touch, metallic minerals have the lustre of polished metal, and with ideal surfaces will work as a reflective surface. Examples include galena, pyrite and magnetite, pearly minerals consist of thin transparent co-planar sheets. Light reflecting from these layers give them a lustre reminiscent of pearls, such minerals possess perfect cleavage, with examples including muscovite and stilbite. Resinous minerals have the appearance of resin, chewing gum or plastic, a principal example is amber, which is a form of fossilized resin. Silky minerals have an arrangement of extremely fine fibres, giving them a lustre reminiscent of silk. Examples include asbestos, ulexite and the satin spar variety of gypsum, a fibrous lustre is similar, but has a coarser texture
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Streak (mineralogy)
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The streak of a mineral is the color of the powder produced when it is dragged across an un-weathered surface. If no streak seems to be made, the streak is said to be white or colorless. Streak is particularly important as a diagnostic for opaque and colored materials and it is less useful for silicate minerals, most of which have a white streak or are too hard to powder easily. The apparent color of a mineral can vary widely because of impurities or a disturbed macroscopic crystal structure. Small amounts of an impurity that strongly absorbs a particular wavelength can radically change the wavelengths of light that are reflected by the specimen, and thus change the apparent color. However, when the specimen is dragged to produce a streak, it is broken into randomly oriented microscopic crystals, the surface across which the mineral is dragged is called a streak plate, and is generally made of unglazed porcelain tile. In the absence of a plate, the unglazed underside of a porcelain bowl or vase or the back of a glazed tile will work. Sometimes a streak is more easily or accurately described by comparing it with the streak made by another streak plate. Because the trail left behind results from the mineral being crushed into powder, in case of harder minerals, the color of the powder can be determined by filing or crushing with a hammer a small sample, which is then usually rubbed on a streak plate. Most minerals that are harder have a white streak. Some minerals leave a similar to their natural color, such as cinnabar. Other minerals leave surprising colors, such as fluorite, which always has a streak, although it can appear in purple, blue, yellow. Hematite, which is black in appearance, leaves a red streak which accounts for its name, galena, which can be similar in appearance to hematite, is easily distinguished by its gray streak. Hamilton, W. R. Cambridge Guide to Minerals, Rocks, the Encyclopedia of Gemstones and Minerals. New York, Facts on File. p.251, physical Characteristics of Minerals, at Introduction to Mineralogy by Andrea Bangert What is Streak
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Transparency and translucency
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In the field of optics, transparency is the physical property of allowing light to pass through the material without being scattered. On a macroscopic scale, the photons can be said to follow Snells Law, in other words, a translucent medium allows the transport of light while a transparent medium not only allows the transport of light but allows for image formation. The opposite property of translucency is opacity, transparent materials appear clear, with the overall appearance of one color, or any combination leading up to a brilliant spectrum of every color. When light encounters a material, it can interact with it in different ways. These interactions depend on the wavelength of the light and the nature of the material, photons interact with an object by some combination of reflection, absorption and transmission. Some materials, such as glass and clean water, transmit much of the light that falls on them and reflect little of it. Many liquids and aqueous solutions are highly transparent, absence of structural defects and molecular structure of most liquids are mostly responsible for excellent optical transmission. Materials which do not transmit light are called opaque, many such substances have a chemical composition which includes what are referred to as absorption centers. Many substances are selective in their absorption of light frequencies. They absorb certain portions of the spectrum while reflecting others. The frequencies of the spectrum which are not absorbed are either reflected or transmitted for our physical observation and this is what gives rise to color. The attenuation of light of all frequencies and wavelengths is due to the mechanisms of absorption. Transparency can provide almost perfect camouflage for animals able to achieve it and this is easier in dimly-lit or turbid seawater than in good illumination. Many marine animals such as jellyfish are highly transparent, at the atomic or molecular level, physical absorption in the infrared portion of the spectrum depends on the frequencies of atomic or molecular vibrations or chemical bonds, and on selection rules. Nitrogen and oxygen are not greenhouse gases because there is no absorption because there is no molecular dipole moment. With regard to the scattering of light, the most critical factor is the scale of any or all of these structural features relative to the wavelength of the light being scattered. Primary material considerations include, Crystalline structure, whether or not the atoms or molecules exhibit the long-range order evidenced in crystalline solids, glassy structure, scattering centers include fluctuations in density or composition. Microstructure, scattering centers include internal surfaces such as boundaries, crystallographic defects
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Specific gravity
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This page is about the measurement using water as a reference. For a general use of gravity, see relative density. See intensive property for the property implied by specific, Apparent specific gravity is the ratio of the weight of a volume of the substance to the weight of an equal volume of the reference substance. The reference substance is always water at its densest for liquids. Nonetheless, the temperature and pressure must be specified for both the sample and the reference, pressure is nearly always 1 atm. Temperatures for both sample and reference vary from industry to industry, in British beer brewing, the practice for specific gravity as specified above is to multiply it by 1000. Being a ratio of densities, specific gravity is a dimensionless quantity, Specific gravity varies with temperature and pressure, reference and sample must be compared at the same temperature and pressure or be corrected to a standard reference temperature and pressure. Substances with a gravity of 1 are neutrally buoyant in water. Those with SG greater than 1 are denser than water and will, disregarding surface tension effects and those with an SG less than 1 are less dense than water and will float on it. In scientific work, the relationship of mass to volume is expressed directly in terms of the density of the substance under study. It is in industry where specific gravity finds wide application, often for historical reasons. True specific gravity can be expressed mathematically as, S G true = ρ sample ρ H2 O where ρ sample is the density of the sample, the density of water varies with temperature and pressure as does the density of the sample. So it is necessary to specify the temperatures and pressures at which the densities or weights were determined and it is nearly always the case that measurements are made at 1 nominal atmosphere. For true specific gravity calculations, air pressure must be considered, temperatures are specified by the notation with T s representing the temperature at which the samples density was determined and T r the temperature at which the reference density is specified. For example, SG would be understood to mean that the density of the sample was determined at 20°C and of the water at 4°C. Taking into account different sample and reference temperatures, we note that, while S G H2 O =1.000000, it is also the case that S G H2 O =0.998203 /0.999840 =0.998363. Here, temperature is being specified using the current ITS-90 scale, on the previous IPTS-68 scale, the densities at 20 °C and 4 °C are 0.9982071 and 0.9999720 respectively, resulting in an SG value for water of 0.9982343. For example, in the industry, the Plato table lists sucrose concentration by weight against true SG
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Density
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The density, or more precisely, the volumetric mass density, of a substance is its mass per unit volume. The symbol most often used for density is ρ, although the Latin letter D can also be used. Mathematically, density is defined as mass divided by volume, ρ = m V, where ρ is the density, m is the mass, and V is the volume. In some cases, density is defined as its weight per unit volume. For a pure substance the density has the numerical value as its mass concentration. Different materials usually have different densities, and density may be relevant to buoyancy, purity, osmium and iridium are the densest known elements at standard conditions for temperature and pressure but certain chemical compounds may be denser. Thus a relative density less than one means that the floats in water. The density of a material varies with temperature and pressure and this variation is typically small for solids and liquids but much greater for gases. Increasing the pressure on an object decreases the volume of the object, increasing the temperature of a substance decreases its density by increasing its volume. In most materials, heating the bottom of a results in convection of the heat from the bottom to the top. This causes it to rise relative to more dense unheated material, the reciprocal of the density of a substance is occasionally called its specific volume, a term sometimes used in thermodynamics. Density is a property in that increasing the amount of a substance does not increase its density. Archimedes knew that the irregularly shaped wreath could be crushed into a cube whose volume could be calculated easily and compared with the mass, upon this discovery, he leapt from his bath and ran naked through the streets shouting, Eureka. As a result, the term eureka entered common parlance and is used today to indicate a moment of enlightenment, the story first appeared in written form in Vitruvius books of architecture, two centuries after it supposedly took place. Some scholars have doubted the accuracy of this tale, saying among other things that the method would have required precise measurements that would have been difficult to make at the time, from the equation for density, mass density has units of mass divided by volume. As there are units of mass and volume covering many different magnitudes there are a large number of units for mass density in use. The SI unit of kilogram per metre and the cgs unit of gram per cubic centimetre are probably the most commonly used units for density.1,000 kg/m3 equals 1 g/cm3. In industry, other larger or smaller units of mass and or volume are often more practical, see below for a list of some of the most common units of density
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Refractive index
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In optics, the refractive index or index of refraction n of a material is a dimensionless number that describes how light propagates through that medium. It is defined as n = c v, where c is the speed of light in vacuum, for example, the refractive index of water is 1.333, meaning that light travels 1.333 times faster in a vacuum than it does in water. The refractive index determines how light is bent, or refracted. The refractive indices also determine the amount of light that is reflected when reaching the interface, as well as the angle for total internal reflection. This implies that vacuum has a index of 1. The refractive index varies with the wavelength of light and this is called dispersion and causes the splitting of white light into its constituent colors in prisms and rainbows, and chromatic aberration in lenses. Light propagation in absorbing materials can be described using a refractive index. The imaginary part then handles the attenuation, while the real part accounts for refraction, the concept of refractive index is widely used within the full electromagnetic spectrum, from X-rays to radio waves. It can also be used with wave phenomena such as sound, in this case the speed of sound is used instead of that of light and a reference medium other than vacuum must be chosen. Thomas Young was presumably the person who first used, and invented, at the same time he changed this value of refractive power into a single number, instead of the traditional ratio of two numbers. The ratio had the disadvantage of different appearances, newton, who called it the proportion of the sines of incidence and refraction, wrote it as a ratio of two numbers, like 529 to 396. Hauksbee, who called it the ratio of refraction, wrote it as a ratio with a fixed numerator, hutton wrote it as a ratio with a fixed denominator, like 1.3358 to 1. Young did not use a symbol for the index of refraction, in the next years, others started using different symbols, n, m, and µ. For visible light most transparent media have refractive indices between 1 and 2, a few examples are given in the adjacent table. These values are measured at the yellow doublet D-line of sodium, with a wavelength of 589 nanometers, gases at atmospheric pressure have refractive indices close to 1 because of their low density. Almost all solids and liquids have refractive indices above 1.3, aerogel is a very low density solid that can be produced with refractive index in the range from 1.002 to 1.265. Moissanite lies at the end of the range with a refractive index as high as 2.65. Most plastics have refractive indices in the range from 1.3 to 1.7, for infrared light refractive indices can be considerably higher
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Birefringence
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Birefringence is the optical property of a material having a refractive index that depends on the polarization and propagation direction of light. These optically anisotropic materials are said to be birefringent, the birefringence is often quantified as the maximum difference between refractive indices exhibited by the material. Crystals with non-cubic crystal structures are often birefringent, as are plastics under mechanical stress and this effect was first described by the Danish scientist Rasmus Bartholin in 1669, who observed it in calcite, a crystal having one of the strongest birefringences. A mathematical description of wave propagation in a birefringent medium is presented below, following is a qualitative explanation of the phenomenon. Thus rotating the material around this axis does not change its optical behavior and this special direction is known as the optic axis of the material. Light whose polarization is perpendicular to the axis is governed by a refractive index no. Light whose polarization is in the direction of the optic axis sees an optical index ne, for any ray direction there is a linear polarization direction perpendicular to the optic axis, and this is called an ordinary ray. The magnitude of the difference is quantified by the birefringence, Δ n = n e − n o, the propagation of the ordinary ray is simply described by no as if there were no birefringence involved. However the extraordinary ray, as its name suggests, propagates unlike any wave in an optical material. Its refraction at a surface can be using the effective refractive index. However it is in fact an inhomogeneous wave whose power flow is not exactly in the direction of the wave vector and this causes an additional shift in that beam, even when launched at normal incidence, as is popularly observed using a crystal of calcite as photographed above. Rotating the calcite crystal will cause one of the two images, that of the ray, to rotate slightly around that of the ordinary ray. When the light propagates either along or orthogonal to the optic axis, in the first case, both polarizations see the same effective refractive index, so there is no extraordinary ray. In the second case the extraordinary ray propagates at a different phase velocity but is not an inhomogeneous wave, for instance, a quarter-wave plate is commonly used to create circular polarization from a linearly polarized source. The case of so-called biaxial crystals is substantially more complex and these are characterized by three refractive indices corresponding to three principal axes of the crystal. For most ray directions, both polarizations would be classified as extraordinary rays but with different effective refractive indices, being extraordinary waves, however, the direction of power flow is not identical to the direction of the wave vector in either case. The two refractive indices can be determined using the index ellipsoids for given directions of the polarization, note that for biaxial crystals the index ellipsoid will not be an ellipsoid of revolution but is described by three unequal principle refractive indices nα, nβ and nγ. Thus there is no axis around which a rotation leaves the optical properties invariant, for this reason, birefringent materials with three distinct refractive indices are called biaxial
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Pleochroism
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Pleochroism is an optical phenomenon in which a substance appears to be different colors when observed at different angles, especially with polarized light. Anisotropic crystals will have properties that vary with the direction of light. The polarization of light determines the direction of the electric field and these kinds of crystals have one or two optical axes. If absorption of light varies with the relative to the optical axis in a crystal then pleochroism results. Anisotropic crystals have double refraction of light where light of different polarizations is bent different amounts by the crystal, the components of a divided light beam follow different paths within the mineral and travel at different speeds. When the mineral is observed at some angle, light following some combination of paths and polarizations will be present, at another angle, the light passing through the crystal will be composed of another combination of light paths and polarizations, each with their own color. The light passing through the mineral will therefore have different colors when it is viewed from different angles, tetragonal, trigonal and hexagonal minerals can only show two colors and are called dichroic. Orthorhombic, monoclinic and triclinic crystals can show three and are trichroic, for example, hypersthene, with two optical axes, can have red, yellow or blue appearance when oriented in three different ways in three-dimensional space. Tourmaline is notable for exhibiting strong pleochroism, gems are sometimes cut and set either to display pleochroism or to hide it, depending on the colors and their attractiveness. The pleochroic colours are at their maximum when light is polarized parallel with a crystallographic axis, the axes are designated X, Y and Z. These axes can be determined from the appearance of a crystal in an interference pattern. Where there are two axes, the acute bisection of the axes gives Z for positive minerals and X for negative minerals. Perpendicular to these is the Y axis, the colour is measured with the polarization parallel to each direction. An absorption formula records the amount of parallel to each axis in the form of X < Y < Z with the left most having the least absorption. Minerals that are very similar often have very different pleochroic color schemes. In such cases, a section of the mineral is used and examined under polarized transmitted light with a petrographic microscope. Another device using this property to identify minerals is the dichroscope
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Mineral
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A mineral is a naturally occurring chemical compound, usually of crystalline form and abiogenic in origin. A mineral has one specific chemical composition, whereas a rock can be an aggregate of different minerals or mineraloids, the study of minerals is called mineralogy. There are over 5,300 known mineral species, over 5,070 of these have been approved by the International Mineralogical Association, the silicate minerals compose over 90% of the Earths crust. The diversity and abundance of species is controlled by the Earths chemistry. Silicon and oxygen constitute approximately 75% of the Earths crust, which translates directly into the predominance of silicate minerals, minerals are distinguished by various chemical and physical properties. Differences in chemical composition and crystal structure distinguish the various species, changes in the temperature, pressure, or bulk composition of a rock mass cause changes in its minerals. Minerals can be described by their various properties, which are related to their chemical structure. Common distinguishing characteristics include crystal structure and habit, hardness, lustre, diaphaneity, colour, streak, tenacity, cleavage, fracture, parting, more specific tests for describing minerals include magnetism, taste or smell, radioactivity and reaction to acid. Minerals are classified by key chemical constituents, the two dominant systems are the Dana classification and the Strunz classification, the silicate class of minerals is subdivided into six subclasses by the degree of polymerization in the chemical structure. All silicate minerals have a unit of a 4− silica tetrahedron—that is, a silicon cation coordinated by four oxygen anions. These tetrahedra can be polymerized to give the subclasses, orthosilicates, disilicates, cyclosilicates, inosilicates, phyllosilicates, other important mineral groups include the native elements, sulfides, oxides, halides, carbonates, sulfates, and phosphates. The first criterion means that a mineral has to form by a natural process, stability at room temperature, in the simplest sense, is synonymous to the mineral being solid. More specifically, a compound has to be stable or metastable at 25 °C, modern advances have included extensive study of liquid crystals, which also extensively involve mineralogy. Minerals are chemical compounds, and as such they can be described by fixed or a variable formula, many mineral groups and species are composed of a solid solution, pure substances are not usually found because of contamination or chemical substitution. Finally, the requirement of an ordered atomic arrangement is usually synonymous with crystallinity, however, crystals are also periodic, an ordered atomic arrangement gives rise to a variety of macroscopic physical properties, such as crystal form, hardness, and cleavage. There have been recent proposals to amend the definition to consider biogenic or amorphous substances as minerals. The formal definition of an approved by the IMA in 1995, A mineral is an element or chemical compound that is normally crystalline. However, if geological processes were involved in the genesis of the compound, Mineral classification schemes and their definitions are evolving to match recent advances in mineral science
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Earth
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Earth, otherwise known as the World, or the Globe, is the third planet from the Sun and the only object in the Universe known to harbor life. It is the densest planet in the Solar System and the largest of the four terrestrial planets, according to radiometric dating and other sources of evidence, Earth formed about 4.54 billion years ago. Earths gravity interacts with objects in space, especially the Sun. During one orbit around the Sun, Earth rotates about its axis over 365 times, thus, Earths axis of rotation is tilted, producing seasonal variations on the planets surface. The gravitational interaction between the Earth and Moon causes ocean tides, stabilizes the Earths orientation on its axis, Earths lithosphere is divided into several rigid tectonic plates that migrate across the surface over periods of many millions of years. About 71% of Earths surface is covered with water, mostly by its oceans, the remaining 29% is land consisting of continents and islands that together have many lakes, rivers and other sources of water that contribute to the hydrosphere. The majority of Earths polar regions are covered in ice, including the Antarctic ice sheet, Earths interior remains active with a solid iron inner core, a liquid outer core that generates the Earths magnetic field, and a convecting mantle that drives plate tectonics. Within the first billion years of Earths history, life appeared in the oceans and began to affect the Earths atmosphere and surface, some geological evidence indicates that life may have arisen as much as 4.1 billion years ago. Since then, the combination of Earths distance from the Sun, physical properties, in the history of the Earth, biodiversity has gone through long periods of expansion, occasionally punctuated by mass extinction events. Over 99% of all species that lived on Earth are extinct. Estimates of the number of species on Earth today vary widely, over 7.4 billion humans live on Earth and depend on its biosphere and minerals for their survival. Humans have developed diverse societies and cultures, politically, the world has about 200 sovereign states, the modern English word Earth developed from a wide variety of Middle English forms, which derived from an Old English noun most often spelled eorðe. It has cognates in every Germanic language, and their proto-Germanic root has been reconstructed as *erþō, originally, earth was written in lowercase, and from early Middle English, its definite sense as the globe was expressed as the earth. By early Modern English, many nouns were capitalized, and the became the Earth. More recently, the name is simply given as Earth. House styles now vary, Oxford spelling recognizes the lowercase form as the most common, another convention capitalizes Earth when appearing as a name but writes it in lowercase when preceded by the. It almost always appears in lowercase in colloquial expressions such as what on earth are you doing, the oldest material found in the Solar System is dated to 4. 5672±0.0006 billion years ago. By 4. 54±0.04 Gya the primordial Earth had formed, the formation and evolution of Solar System bodies occurred along with the Sun
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Continental crust
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The continental crust is the layer of igneous, sedimentary, and metamorphic rocks that forms the continents and the areas of shallow seabed close to their shores, known as continental shelves. This layer is sometimes called sial because its composition is more felsic compared to the oceanic crust. The continental crust consists of layers, with a bulk composition that is intermediate to felsic. The average density of continental crust is about 2.7 g/cm3, less dense than the material that makes up the mantle. Continental crust is less dense than oceanic crust, whose density is about 2.9 g/cm3. At 25 to 70 km, continental crust is thicker than oceanic crust. About 40% of Earths surface is occupied by continental crust. It makes up about 70% of the volume of Earths crust, because the surface of continental crust mainly lies above sea level, its existence allowed land life to evolve from marine life. There is little evidence of continental crust prior to 3.5 Ga, all continental crust ultimately derives from the fractional differentiation of oceanic crust over many eons. This process has been and continues today primarily as a result of the associated with subduction. In contrast to the persistence of continental crust, the size, shape, different tracts rift apart, collide and recoalesce as part of a grand supercontinent cycle. There are currently about 7 billion cubic kilometers of continental crust, the relative permanence of continental crust contrasts with the short life of oceanic crust. Because continental crust is less dense oceanic crust, when active margins of the two meet in subduction zones, the oceanic crust is typically subducted back into the mantle. Continental crust is rarely subducted.01 Ga, whereas the oldest oceanic crust is from the Jurassic, Continental crust and the rock layers that lie on and within it are thus the best archive of Earths history. The height of mountain ranges is usually related to the thickness of crust and this results from the isostasy associated with orogeny. The crust is thickened by the compressive forces related to subduction or continental collision, the buoyancy of the crust forces it upwards, the forces of the collisional stress balanced by gravity and erosion. This forms a keel or mountain root beneath the mountain range, the thinnest continental crust is found in rift zones, where the crust is thinned by detachment faulting and eventually severed, replaced by oceanic crust. The edges of continental fragments formed this way are termed passive margins, igneous rock may also be underplated to the underside of the crust, i. e. adding to the crust by forming a layer immediately beneath it
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Crystal
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A crystal or crystalline solid is a solid material whose constituents are arranged in a highly ordered microscopic structure, forming a crystal lattice that extends in all directions. In addition, macroscopic single crystals are usually identifiable by their geometrical shape, the scientific study of crystals and crystal formation is known as crystallography. The process of crystal formation via mechanisms of crystal growth is called crystallization or solidification, the word crystal derives from the Ancient Greek word κρύσταλλος, meaning both ice and rock crystal, from κρύος, icy cold, frost. Examples of large crystals include snowflakes, diamonds, and table salt, most inorganic solids are not crystals but polycrystals, i. e. many microscopic crystals fused together into a single solid. Examples of polycrystals include most metals, rocks, ceramics, a third category of solids is amorphous solids, where the atoms have no periodic structure whatsoever. Examples of amorphous solids include glass, wax, and many plastics, Crystals are often used in pseudoscientific practices such as crystal therapy, and, along with gemstones, are sometimes associated with spellwork in Wiccan beliefs and related religious movements. The scientific definition of a crystal is based on the arrangement of atoms inside it. A crystal is a solid where the form a periodic arrangement. For example, when liquid water starts freezing, the change begins with small ice crystals that grow until they fuse. Most macroscopic inorganic solids are polycrystalline, including almost all metals, ceramics, ice, rocks, solids that are neither crystalline nor polycrystalline, such as glass, are called amorphous solids, also called glassy, vitreous, or noncrystalline. These have no periodic order, even microscopically, there are distinct differences between crystalline solids and amorphous solids, most notably, the process of forming a glass does not release the latent heat of fusion, but forming a crystal does. A crystal structure is characterized by its cell, a small imaginary box containing one or more atoms in a specific spatial arrangement. The unit cells are stacked in three-dimensional space to form the crystal, the symmetry of a crystal is constrained by the requirement that the unit cells stack perfectly with no gaps. There are 219 possible crystal symmetries, called space groups. These are grouped into 7 crystal systems, such as cubic crystal system or hexagonal crystal system, Crystals are commonly recognized by their shape, consisting of flat faces with sharp angles. Euhedral crystals are those with obvious, well-formed flat faces, anhedral crystals do not, usually because the crystal is one grain in a polycrystalline solid. The flat faces of a crystal are oriented in a specific way relative to the underlying atomic arrangement of the crystal. This occurs because some surface orientations are more stable than others, as a crystal grows, new atoms attach easily to the rougher and less stable parts of the surface, but less easily to the flat, stable surfaces
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Magma
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Besides molten rock, magma may also contain suspended crystals, dissolved gas and sometimes gas bubbles. Magma often collects in magma chambers that may feed a volcano or solidify underground to form an intrusion, magma is capable of intruding into adjacent rocks, extrusion onto the surface as lava, and explosive ejection as tephra to form pyroclastic rock. Magma is a complex high-temperature fluid substance, temperatures of most magmas are in the range 700 °C to 1300 °C, but very rare carbonatite magmas may be as cool as 600 °C, and komatiite magmas may have been as hot as 1600 °C. Environments of magma formation and compositions are commonly correlated, environments include subduction zones, continental rift zones, mid-ocean ridges and hotspots. Despite being found in such locales, the bulk of the Earths crust. Except for the outer core, most of the Earth takes the form of a rheid. Magma, as liquid, preferentially forms in high temperature, low pressure environments within several kilometers of the Earths surface, magma compositions may evolve after formation by fractional crystallization, contamination, and magma mixing. By definition rock formed of solidified magma is called igneous rock, melting of solid rocks to form magma is controlled by three physical parameters, temperature, pressure, and composition. Mechanisms are discussed in the entry for igneous rock, as a rock melts, its volume changes. When enough rock is melted, the small globules of melt link up, under pressure within the earth, as little as a fraction of a percent partial melting may be sufficient to cause melt to be squeezed from its source. The degree of melting is critical for determining what type of magma is produced. The degree of partial melting required to form a melt can be estimated by considering the relative enrichment of incompatible elements versus compatible elements, incompatible elements commonly include potassium, barium, cesium, and rubidium. Rock types produced by small degrees of melting in the Earths mantle are typically alkaline. Typically, primitive melts of this composition form lamprophyre, lamproite, kimberlite and sometimes nepheline-bearing mafic rocks such as alkali basalts, pegmatite may be produced by low degrees of partial melting of the crust. Some granite-composition magmas are eutectic melts, and they may be produced by low to high degrees of melting of the crust. At high degrees of melting of the crust, granitoids such as tonalite, granodiorite and monzonite can be produced. Being only the time in recorded history that magma had been reached, IDDP decided to invest in the hole. A cemented steel case was constructed in the hole with a perforation at the close to the magma
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Vein (geology)
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In geology, a vein is a distinct sheetlike body of crystallized minerals within a rock. Veins form when mineral constituents carried by a solution within the rock mass are deposited through precipitation. The hydraulic flow involved is usually due to hydrothermal circulation and this certainly is the method for the formation of some veins. However, it is rare in geology for significant open space to open in large volumes of rock. Thus, there are two main mechanisms considered likely for the formation of veins, open-space filling and crack-seal growth, open space filling is the hallmark of epithermal vein systems, such as a stockwork, in greisens or in certain skarn environments. For open space filling to take effect, the pressure is generally considered to be below 0.5 GPa. Often evidence of fluid boiling is present, vugs, cavities and geodes are all examples of open-space filling phenomena in hydrothermal systems. Alternatively, hydraulic fracturing may create a breccia which is filled with vein material, when the confining pressure is too great, or when brittle-ductile rheological conditions predominate, vein formation occurs via crack-seal mechanisms. Crack-seal veins are thought to form quite quickly during deformation by precipitation of minerals within incipient fractures and this happens swiftly by geologic standards, because pressures and deformation mean that large open spaces cannot be maintained, generally the space is in the order of millimeters or micrometers. Veins grow in thickness by reopening of the fracture and progressive deposition of minerals on the growth surface. Veins generally need either hydraulic pressure in excess of pressure or they need open spaces or fractures. In all cases except brecciation, therefore, a vein measures the plane of extension within the rock mass, measurement of enough veins will statistically form a plane of principal extension. In ductilely deforming compressional regimes, this can in turn give information on the stresses active at the time of vein formation, in extensionally deforming regimes, the veins occur roughly normal to the axis of extension. Veins are of importance to mineral deposits, because they are the source of mineralisation either in or proximal to the veins. Typical examples include gold lodes, as well as skarn mineralisation, hydrofracture breccias are classic targets for ore exploration as there is plenty of fluid flow and open space to deposit ore minerals. Ores related to hydrothermal mineralisation, which are associated with vein material, in many gold mines exploited during the gold rushes of the 19th century, vein material alone was typically sought as ore material. In most of todays mines, ore material is composed of the veins. The difference between 19th-century and 21st-century mining techniques and the type of ore sought is based on the grade of material being mined and the methods of mining which are used
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Intrusive rock
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Intrusive rock is formed when magma crystallizes and solidifies underground to form intrusions, for example plutons, batholiths, dikes, sills, laccoliths, and volcanic necks. Intrusive rock forms within Earths crust from the crystallization of magma, magma slowly pushes up from deep within the earth into any cracks or spaces it can find, sometimes pushing existing country rock out of the way, a process that can take millions of years. As the magma slowly cools into a solid, the different parts of the magma crystallize into rocks, many mountain ranges, such as the Sierra Nevada in California, are formed mostly from large granite intrusions, see Sierra Nevada Batholith. Intrusions are one of the two ways igneous rock can form, the other is extrusive rock, that is, an eruption or similar event. Technically speaking, an intrusion is any formation of igneous rock, rock formed from magma that cools. In contrast, an extrusion consists of rock, rock formed above the surface of the crust. Large bodies of magma that solidify underground before they reach the surface of the crust are called plutons, plutonic rocks form 7% of the Earths current land surface. Coarse-grained intrusive igneous rocks form at depth within the earth are called abyssal while those that form near the surface are called subvolcanic or hypabyssal. The term intrusive suite seems near synonymous, there is, however, a modest difference, An intrusive suite is a group of plutons related in time and space. Intrusions vary widely, from mountain-range-sized batholiths to thin veinlike fracture fillings of aplite or pegmatite, when exposed by erosion, such batholiths may occupy large areas. A well-known example of an intrusion is Devils Tower, another is Shiprock, New Mexico, USA. Be the pluton is large, it may be called a batholith or a stock, Intrusive rocks are characterized by large crystal sizes, and as the individual crystals are visible, the rock is called phaneritic. This is as the magma cools underground, and while cooling may be fast or slow, cooling is slower than on the surface, if it runs parallel to rock layers, it is called a sill. If an intrusion makes rocks above rise to form a dome, as heat dissipation is slow, and as the rock is under pressure, crystals form, and no vitreous rapidly chilled matter is present. The intrusions did not flow while solidifying, hence do not show lines, contained gases could not escape through the thick strata, thus form cavities, which can often be observed. Because their crystals are of the rough equal size, these rocks are said to be equigranular, there is typically no distinction between a first generation of large well-shaped crystals and a fine-grained ground-mass. Earlier crystals originated at a time when most of the rock was still liquid and are more or less perfect, later crystals are less regular in shape because they were compelled to occupy the spaces left between the already-formed crystals. The former case is said to be idiomorphic, the latter is xenomorphic, there are also many other characteristics that serve to distinguish the members of these two groups
32.
Igneous rock
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Igneous rock, or magmatic rock, is one of the three main rock types, the others being sedimentary and metamorphic. Igneous rock is formed through the cooling and solidification of magma or lava, the magma can be derived from partial melts of existing rocks in either a planets mantle or crust. Typically, the melting is caused by one or more of three processes, an increase in temperature, a decrease in pressure, or a change in composition, solidification into rock occurs either below the surface as intrusive rocks or on the surface as extrusive rocks. Igneous rock may form with crystallization to form granular, crystalline rocks, Igneous and metamorphic rocks make up 90–95% of the top 16 km of the Earths crust by volume. Igneous rocks form about 15% of the Earths current land surface, most of the Earths oceanic crust is made of igneous rock. In terms of modes of occurrence, igneous rocks can be either intrusive or extrusive, the mineral grains in such rocks can generally be identified with the naked eye. Intrusive rocks can also be classified according to the shape and size of the intrusive body, typical intrusive formations are batholiths, stocks, laccoliths, sills and dikes. When the magma solidifies within the earths crust, it cools slowly forming coarse textured rocks, such as granite, gabbro, the central cores of major mountain ranges consist of intrusive igneous rocks, usually granite. When exposed by erosion, these cores may occupy huge areas of the Earths surface, intrusive igneous rocks that form at depth within the crust are termed plutonic rocks and are usually coarse-grained. Intrusive igneous rocks that form near the surface are termed subvolcanic or hypabyssal rocks, hypabyssal rocks are less common than plutonic or volcanic rocks and often form dikes, sills, laccoliths, lopoliths, or phacoliths. Extrusive igneous rocks, also known as rocks, are formed at the crusts surface as a result of the partial melting of rocks within the mantle. Extrusive igneous rocks cool and solidify quicker than intrusive igneous rocks and they are formed by the cooling of molten magma on the earths surface. The magma, which is brought to the surface through fissures or volcanic eruptions, hence such rocks are smooth, crystalline and fine-grained. Basalt is an extrusive igneous rock and forms lava flows, lava sheets. Some kinds of basalt solidify to form long polygonal columns, the Giants Causeway in Antrim, Northern Ireland is an example. The molten rock, with or without suspended crystals and gas bubbles, is called magma and it rises because it is less dense than the rock from which it was created. When magma reaches the surface from beneath water or air, it is called lava, eruptions of volcanoes into air are termed subaerial, whereas those occurring underneath the ocean are termed submarine. Black smokers and mid-ocean ridge basalt are examples of volcanic activity
33.
Metamorphic rock
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Metamorphic rocks arise from the transformation of existing rock types, in a process called metamorphism, which means change in form. The original rock is subjected to heat and pressure, causing profound physical and/or chemical change, the protolith may be a sedimentary, an igneous, or even an existing type of metamorphic rock. Metamorphic rocks make up a part of the Earths crust. They are classified by texture and by chemical and mineral assemblage and they may be formed simply by being deep beneath the Earths surface, subjected to high temperatures and the great pressure of the rock layers above it. They can form from tectonic processes such as continental collisions, which cause horizontal pressure and they are also formed when rock is heated up by the intrusion of hot molten rock called magma from the Earths interior. The study of rocks provides information about the temperatures and pressures that occur at great depths within the Earths crust. Some examples of rocks are gneiss, slate, marble, schist. Metamorphic minerals are those that only at the high temperatures and pressures associated with the process of metamorphism. These minerals, known as index minerals, include sillimanite, kyanite, staurolite, andalusite, and some garnet. Other minerals, such as olivines, pyroxenes, amphiboles, micas, feldspars, and quartz, may be found in metamorphic rocks and these minerals formed during the crystallization of igneous rocks. They are stable at temperatures and pressures and may remain chemically unchanged during the metamorphic process. However, all minerals are only within certain limits. The change in the size of the rock during the process of metamorphism is called recrystallization. Both high temperatures and pressures contribute to recrystallization, high temperatures allow the atoms and ions in solid crystals to migrate, thus reorganizing the crystals, while high pressures cause solution of the crystals within the rock at their point of contact. The layering within metamorphic rocks is called foliation, and it occurs when a rock is being shortened along one axis during recrystallization. This causes the platy or elongated crystals of minerals, such as mica and chlorite and this results in a banded, or foliated rock, with the bands showing the colors of the minerals that formed them. Textures are separated into foliated and non-foliated categories, foliated rock is a product of differential stress that deforms the rock in one plane, sometimes creating a plane of cleavage. For example, slate is a metamorphic rock, originating from shale
34.
Plagioclase
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Plagioclase is a series of tectosilicate minerals within the feldspar group. Rather than referring to a mineral with a specific chemical composition, plagioclase is a continuous solid solution series. This was first shown by the German mineralogist Johann Friedrich Christian Hessel in 1826, the series ranges from albite to anorthite endmembers, where sodium and calcium atoms can substitute for each other in the minerals crystal lattice structure. Plagioclase in hand samples is often identified by its polysynthetic crystal twinning or record-groove effect, plagioclase is a major constituent mineral in the Earths crust, and is consequently an important diagnostic tool in petrology for identifying the composition, origin and evolution of igneous rocks. Plagioclase is also a constituent of rock in the highlands of the Earths moon. Analysis of thermal emission spectra from the surface of Mars suggests that plagioclase is the most abundant mineral in the crust of Mars, the extinction angle is an optical characteristic and varies with the albite fraction. There are several named plagioclase feldspars that fall between albite and anorthite in the series, the following table shows their compositions in terms of constituent anorthite and albite percentages. Anorthite was named by Gustav Rose in 1823 from the Ancient Greek meaning oblique, anorthite is a comparatively rare mineral but occurs in the basic plutonic rocks of some orogenic calc-alkaline suites. Albite is named from the Latin albus, in reference to its pure white color. It is a common and important rock-making mineral associated with the more acid rock types and in pegmatite dikes, often with rarer minerals like tourmaline. The intermediate members of the group are very similar to each other. Bytownite, named after the name for Ottawa, Canada, is a rare mineral occasionally found in more basic rocks. Labradorite is the characteristic feldspar of the basic rock types such as diorite, gabbro, andesite. Labradorite frequently shows an iridescent display of colors due to light refracting within the lamellae of the crystal and it is named after Labrador, where it is a constituent of the intrusive igneous rock anorthosite which is composed almost entirely of plagioclase. A variety of known as spectrolite is found in Finland. Andesine is a mineral of rocks such as diorite which contain a moderate amount of silica. Oligoclase is common in granite, syenite, diorite, and gneiss and it is a frequent associate of orthoclase. The name oligoclase is derived from the Greek for little and fracture, sunstone is mainly oligoclase with flakes of hematite
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Anorthosite
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Anorthosite is a phaneritic, intrusive igneous rock characterized by a predominance of plagioclase feldspar, and a minimal mafic component. Pyroxene, ilmenite, magnetite, and olivine are the minerals most commonly present. Anorthosite on Earth can be divided into two types, Proterozoic anorthosite and Archean anorthosite and these two types of anorthosite have different modes of occurrence, appear to be restricted to different periods in Earths history, and are thought to have had different origins. Lunar anorthosites constitute the areas of the Moons surface and have been the subject of much research. Proterozoic anorthosites were emplaced during the Proterozoic Eon, Anorthosite plutons occur in a wide range of sizes. Some smaller plutons, exemplified by many bodies in the U. S. and Harris in Scotland. Larger plutons, like the Mt. Lister Anorthosite, in northern Labrador, Canada, many Proterozoic anorthosites occur in spatial association with other highly distinctive, contemporaneous rock types. These rock types include iron-rich diorite, gabbro, and norite, leucocratic mafic rocks such as leucotroctolite and leuconorite, importantly, large volumes of ultramafic rocks are not found in association with Proterozoic anorthosites. Occurrences of Proterozoic anorthosites are commonly referred to as massifs, however, there is some question as to what name would best describe any occurrence of anorthosite together with the rock types mentioned above. Batholith is used to such occurrences for the remainder of this article. The areal extent of anorthosite batholiths ranges from small to nearly 20,000 km2, in the instance of the Nain Plutonic Suite in northern Labrador. Major occurrences of Proterozoic anorthosite are found in the southwest U. S. the Appalachian Mountains, eastern Canada, across southern Scandinavia and eastern Europe. Mapped onto the Pangaean continental configuration of that eon, these occurrences are all contained in a single straight belt, the conditions and constraints of this pattern of origin and distribution are not clear. However, see the Origins section below, Anorthosites are also common in layered intrusions. Anorthosite in these layered intrusions can form as cumulate layers in the parts of the intrusive complex or as later-stage intrusions into the layered intrusion complex. Since they are composed of plagioclase feldspar, most of Proterozoic anorthosites appear, in outcrop. Individual plagioclase crystals may be black, white, blue, or grey, the feldspar variety labradorite is commonly present in anorthosites. Mineralogically, labradorite is a term for any calcium-rich plagioclase feldspar containing 50–70 molecular percent anorthite
36.
Sedimentary rock
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Sedimentary rocks are types of rock that are formed by the deposition and subsequent cementation of that material at the Earths surface and within bodies of water. Sedimentation is the name for processes that cause mineral and/or organic particles to settle in place. The particles that form a rock by accumulating are called sediment. Sedimentation may also occur as minerals precipitate from solution or shells of aquatic creatures settle out of suspension. The sedimentary rock cover of the continents of the Earths crust is extensive, sedimentary rocks are only a thin veneer over a crust consisting mainly of igneous and metamorphic rocks. Sedimentary rocks are deposited in layers as strata, forming a structure called bedding, sedimentary rocks are also important sources of natural resources like coal, fossil fuels, drinking water or ores. The study of the sequence of rock strata is the main source for an understanding of the Earths history, including palaeogeography, paleoclimatology. The scientific discipline that studies the properties and origin of rocks is called sedimentology. Sedimentology is part of both geology and physical geography and overlaps partly with other disciplines in the Earth sciences, such as pedology, geomorphology, geochemistry, sedimentary rocks have also been found on Mars. Clastic sedimentary rocks are composed of rock fragments that were cemented by silicate minerals. Clastic rocks are composed largely of quartz, feldspar, rock fragments, clay minerals, and mica, any type of mineral may be present, clastic sedimentary rocks, are subdivided according to the dominant particle size. Most geologists use the Udden-Wentworth grain size scale and divide unconsolidated sediment into three fractions, gravel, sand, and mud and this tripartite subdivision is mirrored by the broad categories of rudites, arenites, and lutites, respectively, in older literature. The subdivision of these three categories is based on differences in clast shape, conglomerates and breccias), composition. Conglomerates are dominantly composed of rounded gravel, while breccias are composed of dominantly angular gravel, composition of framework grains The relative abundance of sand-sized framework grains determines the first word in a sandstone name. Naming depends on the dominance of the three most abundant components quartz, feldspar, or the lithic fragments that originated from other rocks, all other minerals are considered accessories and not used in the naming of the rock, regardless of abundance. Clean sandstones with open space are called arenites. Muddy sandstones with abundant muddy matrix are called wackes, six sandstone names are possible using the descriptors for grain composition and the amount of matrix. Mudrocks are sedimentary rocks composed of at least 50% silt- and clay-sized particles and these relatively fine-grained particles are commonly transported by turbulent flow in water or air, and deposited as the flow calms and the particles settle out of suspension
37.
German language
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German is a West Germanic language that is mainly spoken in Central Europe. It is the most widely spoken and official language in Germany, Austria, Switzerland, South Tyrol, the German-speaking Community of Belgium and it is also one of the three official languages of Luxembourg. Major languages which are most similar to German include other members of the West Germanic language branch, such as Afrikaans, Dutch, English, Luxembourgish and it is the second most widely spoken Germanic language, after English. One of the languages of the world, German is the first language of about 95 million people worldwide. The German speaking countries are ranked fifth in terms of publication of new books. German derives most of its vocabulary from the Germanic branch of the Indo-European language family, a portion of German words are derived from Latin and Greek, and fewer are borrowed from French and English. With slightly different standardized variants, German is a pluricentric language, like English, German is also notable for its broad spectrum of dialects, with many unique varieties existing in Europe and also other parts of the world. The history of the German language begins with the High German consonant shift during the migration period, when Martin Luther translated the Bible, he based his translation primarily on the standard bureaucratic language used in Saxony, also known as Meißner Deutsch. Copies of Luthers Bible featured a long list of glosses for each region that translated words which were unknown in the region into the regional dialect. Roman Catholics initially rejected Luthers translation, and tried to create their own Catholic standard of the German language – the difference in relation to Protestant German was minimal. It was not until the middle of the 18th century that a widely accepted standard was created, until about 1800, standard German was mainly a written language, in urban northern Germany, the local Low German dialects were spoken. Standard German, which was different, was often learned as a foreign language with uncertain pronunciation. Northern German pronunciation was considered the standard in prescriptive pronunciation guides though, however, German was the language of commerce and government in the Habsburg Empire, which encompassed a large area of Central and Eastern Europe. Until the mid-19th century, it was essentially the language of townspeople throughout most of the Empire and its use indicated that the speaker was a merchant or someone from an urban area, regardless of nationality. Some cities, such as Prague and Budapest, were gradually Germanized in the years after their incorporation into the Habsburg domain, others, such as Pozsony, were originally settled during the Habsburg period, and were primarily German at that time. Prague, Budapest and Bratislava as well as cities like Zagreb, the most comprehensive guide to the vocabulary of the German language is found within the Deutsches Wörterbuch. This dictionary was created by the Brothers Grimm and is composed of 16 parts which were issued between 1852 and 1860, in 1872, grammatical and orthographic rules first appeared in the Duden Handbook. In 1901, the 2nd Orthographical Conference ended with a standardization of the German language in its written form
38.
Rock (geology)
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Rock or stone is a natural substance, a solid aggregate of one or more minerals or mineraloids. For example, granite, a rock, is a combination of the minerals quartz, feldspar. The Earths outer solid layer, the lithosphere, is made of rock, rock has been used by mankind throughout history. The minerals and metals found in rocks have been essential to human civilization, three major groups of rocks are defined, igneous, sedimentary, and metamorphic. The scientific study of rocks is called petrology, which is a component of geology. At a granular level, rocks are composed of grains of minerals, the aggregate minerals forming the rock are held together by chemical bonds. The types and abundance of minerals in a rock are determined by the manner in which the rock was formed, many rocks contain silica, a compound of silicon and oxygen that forms 74. 3% of the Earths crust. This material forms crystals with other compounds in the rock, the proportion of silica in rocks and minerals is a major factor in determining their name and properties. Rocks are geologically classified according to such as mineral and chemical composition, permeability, the texture of the constituent particles. These physical properties are the end result of the processes that formed the rocks, over the course of time, rocks can transform from one type into another, as described by the geological model called the rock cycle. These events produce three general classes of rock, igneous, sedimentary, and metamorphic, the three classes of rocks are subdivided into many groups. However, there are no hard and fast boundaries between allied rocks, hence the definitions adopted in establishing rock nomenclature merely correspond to more or less arbitrary selected points in a continuously graduated series. Igneous rock forms through the cooling and solidification of magma or lava and this magma can be derived from partial melts of pre-existing rocks in either a planets mantle or crust. Typically, the melting of rocks is caused by one or more of three processes, an increase in temperature, a decrease in pressure, or a change in composition, igneous rocks are divided into two main categories, plutonic rock and volcanic. Plutonic or intrusive rocks result when magma cools and crystallizes slowly within the Earths crust, a common example of this type is granite. Volcanic or extrusive rocks result from magma reaching the surface either as lava or fragmental ejecta, the chemical abundance and the rate of cooling of magma typically forms a sequence known as Bowens reaction series. Most major igneous rocks are found along this scale, about 64. 7% of the Earths crust by volume consists of igneous rocks, making it the most plentiful category. Of these, 66% are basalts and gabbros, 16% are granite, only 0. 6% are syenites and 0. 3% peridotites and dunites
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Ore
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An ore is a type of rock that contains sufficient minerals with important elements including metals that can be economically extracted from the rock. The ores are extracted from the earth through mining, they are refined to extract the valuable element. The grade or concentration of an ore mineral, or metal, as well as its form of occurrence, will directly affect the costs associated with mining the ore. The cost of extraction must thus be weighed against the value contained in the rock to determine what ore can be processed. Metal ores are generally oxides, sulfides, silicates, or native metals that are not commonly concentrated in the Earths crust, the ores must be processed to extract the metals of interest from the waste rock and from the ore minerals. Ore bodies are formed by a variety of geological processes, the process of ore formation is called ore genesis. An ore deposit is an accumulation of ore and this is distinct from a mineral resource as defined by the mineral resource classification criteria. An ore deposit is one occurrence of a particular ore type, Ore deposits are classified according to various criteria developed via the study of economic geology, or ore genesis. Stratiform arkose-hosted and shale-hosted copper, typified by the Zambian copperbelt and this identifies, early on, whether further investment in estimation and engineering studies is warranted and identifies key risks and areas for further work. This is because the distribution of ores is unequal and dislocated from locations of peak demand. Other, lesser, commodities do not have international clearing houses and benchmark prices and this generally makes determining the price of ores of this nature opaque and difficult. Such metals include lithium, niobium-tantalum, bismuth, antimony and rare earths, most of these commodities are also dominated by one or two major suppliers with >60% of the worlds reserves. The London Metal Exchange aims to add uranium to its list of metals on warrant, the World Bank reports that China was the top importer of ores and metals in 2005 followed by the USA and Japan. Economic geology Mineral resource classification Ore genesis Petrology Froth Flotation Extractive metallurgy DILL, the “chessboard” classification scheme of mineral deposits, Mineralogy and geology from aluminum to zirconium, Earth-Science Reviews, Volume 100, Issue 1-4, June 2010, Pages 1-420
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Spar (mineralogy)
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Spar is an old mining or mineralogy term used to refer to crystals that have readily discernible faces. A spar will easily break or cleave into rhomboidal, cubical, thus, the word spar in mineralogy has the same root as spear, by way of comparison to gypsum, as a common natural crystal forming in spearlike projections. Amongst miners the term today is frequently used alone to express any bright crystalline substance. Most frequently, spar describes easily cleaved, lightly colored nonmetallic minerals such as feldspar, baryte, the main source of barium, is also called heavy spar. Calcite often forms the dogtooth spar crystals found in vugs and caves, generally, a spar will form underwater, either in a phreatic zone, or below the water table, the essential place where most caves form, or in standing pools, as pool spar. If a cave floods and a pool forms, that submerges stalactites, mineral component ions in the water, mostly calcite or gypsum, but sometimes even halite, quartz, and fluorite, are deposited through the course of thousands of years, building up on each other. Sometimes, spar will form in the air due to solutions seeping out of the walls or through porous sediments. When grown in the air, it is made of gypsum or selenite. Sometimes it will form as small needles found in sediments, others spar can be found on the tips of gypsum chandeliers
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Silicate minerals
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Silicate minerals are rock-forming minerals made up of silicate groups. They are the largest and most important class of rock-forming minerals and they are classified based on the structure of their silicate groups, which contain different ratios of silicon and oxygen. Nesosilicates, or orthosilicates, have the orthosilicate ion, which constitute isolated 4− tetrahedra that are connected only by interstitial cations and these exist as 3-member 6− and 6-member 12− rings, where T stands for a tetrahedrally coordinated cation. Inosilicates, or chain silicates, have interlocking chains of silicate tetrahedra with either SiO3,1,3 ratio, for single chains or Si4O11,4,11 ratio, for double chains. Nickel–Strunz classification,09. D Pyroxene group Enstatite – orthoferrosilite series Enstatite – MgSiO3 Ferrosilite – FeSiO3 Pigeonite – Ca0.251, all phyllosilicate minerals are hydrated, with either water or hydroxyl groups attached. Serpentine subgroup Antigorite – Mg3Si2O54 Chrysotile – Mg3Si2O54 Lizardite – Mg3Si2O54 Clay minerals group Halloysite – Al2Si2O54 Kaolinite – Al2Si2O54 Illite – 24O10 Montmorillonite –0 and this group comprises nearly 75% of the crust of the Earth. Tectosilicates, with the exception of the group, are aluminosilicates. Nickel–Strunz classification,09. F and 09. G,04. A, an introduction to the rock-forming minerals. Wise, W. S. Zussman, J. Rock-forming minerals, P.982 pp. Hurlbut, Cornelius S. Danas Manual of Mineralogy. Mindat. org, Dana classification Webmineral, Danas New Silicate Classification Media related to Silicates at Wikimedia Commons
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Orthoclase
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Orthoclase, or orthoclase feldspar, is an important tectosilicate mineral which forms igneous rock. The name is from the Ancient Greek for straight fracture, because its two planes are at right angles to each other. It is a type of potassium feldspar, also known as K-feldspar, the gem known as moonstone is largely composed of orthoclase. Orthoclase is a constituent of most granites and other felsic igneous rocks and often forms huge crystals. Typically, the pure potassium endmember of orthoclase forms a solution with albite. While slowly cooling within the earth, sodium-rich albite lamellae form by exsolution, the resulting intergrowth of the two feldspars is called perthite. The higher-temperature polymorph of KAlSi3O8 is sanidine, sanidine is common in rapidly cooled volcanic rocks such as obsidian and felsic pyroclastic rocks, and is notably found in trachytes of the Drachenfels, Germany. The lower-temperature polymorph of KAlSi3O8 is microcline, adularia is a low temperature form of either microcline or orthoclase originally reported from the low temperature hydrothermal deposits in the Adula Alps of Switzerland. It was first described by Ermenegildo Pini in 1781, the optical effect of adularescence in moonstone is typically due to adularia. The largest documented crystal of orthoclase was found in Ural mountains. It measured ~10×10×0.4 m and weighed ~100 tons, together with the other potassium feldspars, orthoclase is a common raw material for the manufacture of some glasses and some ceramics such as porcelain, and as a constituent of scouring powder. Some intergrowths of orthoclase and albite have an attractive pale luster and are called moonstone when used in jewellery, most moonstones are translucent and white, although grey and peach-colored varieties also occur. In gemology, their luster is called adularescence and is described as creamy or silvery white with a billowy quality. It is the gem of Florida. Orthoclase is one of the ten defining minerals of the Mohs scale of mineral hardness, nASAs Curiosity Rover discovery of high levels of orthoclase in Martian sandstones suggested that some Martian rocks may have experienced complex geological processing, such as repeated melting
43.
Albite
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Albite is a plagioclase feldspar mineral. It is the sodium endmember of the solid solution series. As such it represents a plagioclase with less than 10% anorthite content, the pure albite endmember has the formula NaAlSi3O8. Its color is pure white, hence its name from Latin albus. It is a constituent in felsic rocks. Albite crystallizes with triclinic pinacoidal forms and its specific gravity is about 2.62 and it has a Mohs hardness of 6 -6.5. Albite almost always exhibits crystal twinning often as minute parallel striations on the crystal face, Albite often occurs as fine parallel segregations alternating with pink microcline in perthite as a result of exolution on cooling. There are two variants of albite, which are referred to as low albite and high albite, the latter is known as analbite. Although both variants are triclinic, they differ in the volume of their cell, which is slightly larger for the high form. The high form can be produced from the low form by heating above c.750 °C, upon further heating to more than c.1050 °C the crystal symmetry changes from triclinic to monoclinic, this variant is also known as monalbite. It occurs in granitic and pegmatite masses, in hydrothermal vein deposits. It was first reported in 1815 for an occurrence in Finnbo, Falun, Dalarna and it is used as a gemstone. Mineral galleries This article incorporates text from a now in the public domain, Chisholm, Hugh
44.
Anorthite
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Anorthite is the calcium endmember of plagioclase feldspar. Plagioclase is an abundant mineral in the Earths crust, the formula of pure anorthite is CaAl2Si2O8. Anorthite is the calcium-rich endmember of the solid solution series. Anorthite also refers to plagioclase compositions with more than 90 molecular percent of the anorthite endmember, anorthite is a rare compositional variety of plagioclase. It occurs in igneous rock. It also occurs in rocks of granulite facies, in metamorphosed carbonate rocks. Its type localities are Monte Somma and Valle di Fassa, Italy and it was first described in 1823. It is more rare in surficial rocks than it normally would be due to its high weathering potential in the Goldich dissolution series and it also makes up much of the lunar highlands, the Genesis Rock is made of anorthosite, which is composed largely of anorthite. Anorthite was discovered in samples from comet Wild 2, and the mineral is an important constituent of Ca-Al-rich inclusions in rare varieties of chondritic meteorites
45.
Solid solution
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A solid solution is a solid-state solution of one or more solutes in a solvent. The solid solution needs to be distinguished from a mechanical mixtures of powdered solids like two salts, sugar and salt, etc, the mechanical mixtures have total or partial miscibility gap in solid state. Examples of solid solutions include crystallized salts from their liquid mixture, metal alloys, in the case of metal alloys intermetallic compounds occur frequently. The solute may incorporate into the solvent crystal lattice substitutionally, by replacing a solvent particle in the lattice, or interstitially, by fitting into the space between solvent particles. Both of these types of solid solution affect the properties of the material by distorting the crystal lattice, some mixtures will readily form solid solutions over a range of concentrations, while other mixtures will not form solid solutions at all. The propensity for any two substances to form a solution is a complicated matter involving the chemical, crystallographic. 1 displays an alloy of two metals which forms a solution at all relative concentrations of the two species. Solid solutions have important commercial and industrial applications, as such mixtures often have superior properties to pure materials, many metal alloys are solid solutions. Even small amounts of solute can affect the electrical and physical properties of the solvent, the binary phase diagram in Fig.2 shows the phases of a mixture of two substances in varying concentrations, A and B. The region labeled α is a solution, with B acting as the solute in a matrix of A. On the other end of the scale, the region labeled β is also a solid solution. The large solid region in between the α and β solid solutions, labeled α + β, is not a solid solution, at other proportions, the material will enter a mushy or pasty phase until it warms up to being completely melted. The mixture at the dip point of the diagram is called a eutectic alloy, lead-tin mixtures formulated at that point are useful when soldering electronic components, particularly if done manually, since the solid phase is quickly entered as the solder cools. In contrast, when lead-tin mixtures were used to solder seams in automobile bodies a pasty state enabled a shape to be formed with a paddle or tool. When a solid solution becomes unstable — due to a temperature, for example — exsolution occurs. This is mainly caused by difference in cation size, cations which have a large difference in radii are not likely to readily substitute. Take the alkali feldspar minerals for example, whose end members are albite, NaAlSi3O8 and microcline and this leads to exsolution where they will separate into two separate phases. In the case of the feldspar minerals, thin white albite layers will alternate between typically pink microcline
46.
Miscibility
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Miscibility /mɪsᵻˈbɪlᵻti/ is the property of substances to mix in all proportions, forming a homogeneous solution. The term is most often applied to liquids, but applies also to solids, water and ethanol, for example, are miscible because they mix in all proportions. By contrast, substances are said to be if a significant proportion does not form a solution. Otherwise, the substances are considered miscible, for example, butanone is significantly soluble in water, but these two solvents are not miscible because they are not soluble in all proportions. In organic compounds, the percent of hydrocarbon chain often determines the compounds miscibility with water. For example, among the alcohols, ethanol has two atoms and is miscible with water, whereas 1-octanol with eight carbons is not. Octanols immiscibility leads it to be used as a standard for partition equilibria and this is also the case with lipids, the very long carbon chains of lipids cause them almost always to be immiscible with water. Analogous situations occur for other functional groups, acetic acid is miscible with water, whereas valeric acid is not. Immiscible metals are unable to form alloys with each other, typically, a mixture will be possible in the molten state, but upon freezing the metals separate into layers. This property allows solid precipitates to be formed by freezing a molten mixture of immiscible metals. One example of immiscibility in metals is copper and cobalt, where rapid freezing to form solid precipitates has been used to create granular GMR materials, there also exist metals that are immiscible in the liquid state. One with industrial importance is that liquid zinc and liquid silver are immiscible in liquid lead and this leads to the Parkes process, an example of liquid-liquid extraction, whereby lead containing any amount of silver is melted with zinc. The silver migrates to the zinc, which is skimmed off the top of the liquid. Substances with extremely low configurational entropy, especially polymers, are likely to be immiscible in one even in the liquid state. Miscibility of two materials is often determined optically, when the two miscible liquids are combined, the resulting liquid is clear. If the mixture is cloudy the two materials are immiscible, care must be taken with this determination. If the indices of refraction of the two materials are similar, an immiscible mixture may be clear and give an incorrect determination that the two liquids are miscible, miscibility gap Emulsion Heteroazeotrope ITIES Multiphasic liquid
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This article incorporates public domain material from the United States Geological Survey document: "Feldspar and nepheline syenite" (PDF).
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