1.
Muzo
–
Muzo is a town and municipality in the Western Boyacá Province, part of the department of Boyacá, Colombia. It is widely known as the capital of emeralds for the emerald mines containing the worlds highest quality gems of this type. Muzo is situated at a distance of 178 kilometres from the departmental capital Tunja and 118 kilometres from the capital of the Western Boyacá Province, the urban centre is at an altitude of 815 metres above sea level. Muzo borders Otanche and San Pablo de Borbur in the north, Maripí and Coper in the east, Quípama in the west and the department of Cundinamarca in the south. The town of Muzo was called Villa de la Santísima Trinidad de los Muzos, or simply Trinidad, Muzo is the autonym of the Muzo, the indigenous people who inhabitated the region before the Spanish conquest. The median temperature of Muzo is 26 °C and the annual precipitation 3,152 millimetres, before the Spanish conquest of the Eastern Colombian Andes, the region of Muzo was inhabited by the people with the same name. They extracted emeralds in pre-Columbian times, giving them the name The Emerald People, using poles of hard tropical wood and water, the people peeled the emeralds from the formations, in particular the Muzo Formation, named after the municipality. Historians have estimated the Muzo settled in the area of Muzo around 1000 AD, the Cariban-speaking Muzo, like their Chibcha neighbours, adored the Sun and Moon as deities. Other than their neighbours, they did not construct temples. The first to arrive in Muzo territory was Luis Lanchero, soldier of the conquest expedition led by Nikolaus Federmann and he encountered fierce resistance by the indigenous Muzo and had to return to the newly founded capital Santafe de Bogotá of the New Kingdom of Granada in 1541. The Muzo used the terrain to their advantage and attacked the forty conquistadors, whose horses had problems crossing the hills of Muzo. During a second invasion by the Spanish into the Muzo lands, in 1544, a third campaign to submit the Muzo was executed by conquistador Pedro de Ursúa in 1552. Also he failed to conquer the Muzo, the first evangelisation was performed by Juan de los Barrios in 1566. The Spanish were highly interested in the emeralds of Muzo, proving to be the highest quality emeralds worldwide and they set up encomiendas to guard the valuable gemstones and used the indigenous people to perform slave labour for the extraction of the minerals. The main economical activity with approximately 75% of the income is emerald mining. Agriculture and livestock farming comprise the remaining quarter of the economy of Muzo, agricultural products cultivated are sugarcane, cacao, yuca, avocadoes and citrus fruits. The Muzo mines are situated in the flank of the Eastern ranges of the Colombian Andes. The Devonshire, one of the worlds most famous uncut emeralds, is from the Muzo mines and it is a 1,383.95 carats emerald and was a gift to the 6th Duke of Devonshire by Emperor Dom Pedro I of Brazil in 1831
2.
Colombia
–
Colombia, officially the Republic of Colombia, is a transcontinental country largely situated in the northwest of South America, with territories in Central America. Colombia shares a border to the northwest with Panama, to the east with Venezuela and Brazil and to the south with Ecuador and it shares its maritime limits with Costa Rica, Nicaragua, Honduras, Jamaica, Haiti and the Dominican Republic. It is a unitary, constitutional republic comprising thirty-two departments, the territory of what is now Colombia was originally inhabited by indigenous peoples including the Muisca, the Quimbaya and the Tairona. The Spanish arrived in 1499 and initiated a period of conquest and colonization ultimately creating the Viceroyalty of New Granada, independence from Spain was won in 1819, but by 1830 the Gran Colombia Federation was dissolved. What is now Colombia and Panama emerged as the Republic of New Granada, the new nation experimented with federalism as the Granadine Confederation, and then the United States of Colombia, before the Republic of Colombia was finally declared in 1886. Since the 1960s the country has suffered from an asymmetric low-intensity armed conflict, Colombia is one of the most ethnically and linguistically diverse countries in the world, and thereby possesses a rich cultural heritage. Cultural diversity has also influenced by Colombias varied geography. The urban centres are located in the highlands of the Andes mountains. Colombian territory also encompasses Amazon rainforest, tropical grassland and both Caribbean and Pacific coastlines, ecologically, it is one of the worlds 17 megadiverse countries, and the most densely biodiverse of these per square kilometer. Colombia is a power and a regional actor with the fourth-largest economy in Latin America, is part of the CIVETS group of six leading emerging markets and is an accessing member to the OECD. Colombia has an economy with macroeconomic stability and favorable growth prospects in the long run. The name Colombia is derived from the last name of Christopher Columbus and it was conceived by the Venezuelan revolutionary Francisco de Miranda as a reference to all the New World, but especially to those portions under Spanish and Portuguese rule. The name was adopted by the Republic of Colombia of 1819. When Venezuela, Ecuador and Cundinamarca came to exist as independent states, New Granada officially changed its name in 1858 to the Granadine Confederation. In 1863 the name was changed, this time to United States of Colombia. To refer to country, the Colombian government uses the terms Colombia. Owing to its location, the present territory of Colombia was a corridor of early human migration from Mesoamerica, the oldest archaeological finds are from the Pubenza and El Totumo sites in the Magdalena Valley 100 km southwest of Bogotá. These sites date from the Paleoindian period, at Puerto Hormiga and other sites, traces from the Archaic Period have been found
3.
Beryl
–
Beryl is a mineral composed of beryllium aluminium cyclosilicate with the chemical formula Be3Al26. Well-known varieties of beryl include emerald and aquamarine, naturally occurring, hexagonal crystals of beryl can be up to several meters in size, but terminated crystals are relatively rare. Pure beryl is colorless, but it is tinted by impurities, possible colors are green, blue, yellow, red. The name beryl is derived from Greek βήρυλλος beryllos which referred to a precious blue-green color-of-sea-water stone, akin to Prakrit verulia, the term was later adopted for the mineral beryl more exclusively. When the first eyeglasses were constructed in 13th century Italy, the lenses were made of beryl as glass could not be clear enough. Consequently glasses were named Brillen in German, beryl of various colors is found most commonly in granitic pegmatites, but also occurs in mica schists in the Ural Mountains, and limestone in Colombia. Beryl is often associated with tin and tungsten ore bodies, beryl is found in Europe in Norway, Austria, Germany, Sweden, Ireland and Russia, as well as Brazil, Colombia, Madagascar, Mozambique, Pakistan, South Africa, the United States, and Zambia. US beryl locations are in California, Colorado, Connecticut, Georgia, Idaho, Maine, New Hampshire, North Carolina, South Dakota and Utah. As of 1999, the worlds largest known naturally occurring crystal of any mineral is a crystal of beryl from Malakialina, Madagascar,18 m long and 3.5 m in diameter, aquamarine is a blue or cyan variety of beryl. It occurs at most localities which yield ordinary beryl, the gem-gravel placer deposits of Sri Lanka contain aquamarine. Clear yellow beryl, such as occurring in Brazil, is sometimes called aquamarine chrysolite. The deep blue version of aquamarine is called maxixe, maxixe is commonly found in the country of Madagascar. Its color fades to white when exposed to sunlight or is subjected to heat treatment, the pale blue color of aquamarine is attributed to Fe2+. Fe3+ ions produce golden-yellow color, and when both Fe2+ and Fe3+ are present, the color is a darker blue as in maxixe, decoloration of maxixe by light or heat thus may be due to the charge transfer between Fe3+ and Fe2+. Dark-blue maxixe color can be produced in green, pink or yellow beryl by irradiating it with high-energy particles, in the United States, aquamarines can be found at the summit of Mt. Antero in the Sawatch Range in central Colorado. In Wyoming, aquamarine has been discovered in the Big Horn Mountains, another location within the United States is the Sawtooth Range near Stanley, Idaho, although the minerals are within a wilderness area which prevents collecting. In Brazil, there are mines in the states of Minas Gerais, Espírito Santo, and Bahia, the mines of Colombia, Zambia, Madagascar, Malawi, Tanzania and Kenya also produce aquamarine. The largest aquamarine of gemstone quality ever mined was found in Marambaia, Minas Gerais, Brazil and it weighed over 110 kg, and its dimensions were 48.5 cm long and 42 cm in diameter
4.
Chemical formula
–
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.
Crystal system
–
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
6.
Hexagonal crystal family
–
In crystallography, the hexagonal crystal family is one of the 6 crystal families. In the hexagonal family, the crystal is described by a right rhombic prism unit cell with two equal axes, an included angle of 120° and a height perpendicular to the two base axes. There are 52 space groups associated with it, which are exactly those whose Bravais lattice is either hexagonal or rhombohedral, the hexagonal crystal family consists of two lattice systems, hexagonal and rhombohedral. Each lattice system consists of one Bravais lattice, hence, there are 3 lattice points per unit cell in total and the lattice is non-primitive. The Bravais lattices in the hexagonal crystal family can also be described by rhombohedral axes, the unit cell is a rhombohedron. This is a cell with parameters a = b = c, α = β = γ ≠ 90°. In practice, the description is more commonly used because it is easier to deal with a coordinate system with two 90° angles. However, the axes are often shown in textbooks because this cell reveals 3m symmetry of crystal lattice. However, such a description is rarely used, the hexagonal crystal family consists of two crystal systems, trigonal and hexagonal. A crystal system is a set of point groups in which the point groups themselves, the trigonal crystal system consists of the 5 point groups that have a single three-fold rotation axis. The crystal structures of alpha-quartz in the example are described by two of those 18 space groups associated with the hexagonal lattice system. The hexagonal crystal system consists of the seven point groups such that all their groups have the hexagonal lattice as underlying lattice. Graphite is an example of a crystal that crystallizes in the crystal system. Note that the atom in the center of the HCP unit cell in the hexagonal lattice system does not appear in the unit cell of the hexagonal lattice. It is part of the two atom motif associated with each point in the underlying lattice. The trigonal crystal system is the crystal system whose point groups have more than one lattice system associated with their space groups. The 5 point groups in this system are listed below, with their international number and notation, their space groups in name. The point groups in this system are listed below, followed by their representations in Hermann–Mauguin or international notation and Schoenflies notation
7.
Space group
–
In mathematics, physics and chemistry, a space group is the symmetry group of a configuration in space, usually in three dimensions. In three dimensions, there are 219 distinct types, or 230 if chiral copies are considered distinct, Space groups are also studied in dimensions other than 3 where they are sometimes called Bieberbach groups, and are discrete cocompact groups of isometries of an oriented Euclidean space. In crystallography, space groups are called the crystallographic or Fedorov groups. A definitive source regarding 3-dimensional space groups is the International Tables for Crystallography, in 1879 Leonhard Sohncke listed the 65 space groups whose elements preserve the orientation. More accurately, he listed 66 groups, but Fedorov and Schönflies both noticed that two of them were really the same, the space groups in 3 dimensions were first enumerated by Fedorov, and shortly afterwards were independently enumerated by Schönflies. The correct list of 230 space groups was found by 1892 during correspondence between Fedorov and Schönflies, burckhardt describes the history of the discovery of the space groups in detail. The space groups in three dimensions are made from combinations of the 32 crystallographic point groups with the 14 Bravais lattices, the combination of all these symmetry operations results in a total of 230 different space groups describing all possible crystal symmetries. The elements of the space group fixing a point of space are rotations, reflections, the identity element, the translations form a normal abelian subgroup of rank 3, called the Bravais lattice. There are 14 possible types of Bravais lattice, the quotient of the space group by the Bravais lattice is a finite group which is one of the 32 possible point groups. Translation is defined as the moves from one point to another point. A glide plane is a reflection in a plane, followed by a parallel with that plane. This is noted by a, b or c, depending on which axis the glide is along. There is also the n glide, which is a glide along the half of a diagonal of a face, and the d glide, the latter is called the diamond glide plane as it features in the diamond structure. In 17 space groups, due to the centering of the cell, the glides occur in two directions simultaneously, i. e. the same glide plane can be called b or c, a or b. For example, group Abm2 could be also called Acm2, group Ccca could be called Cccb, in 1992, it was suggested to use symbol e for such planes. The symbols for five groups have been modified, A screw axis is a rotation about an axis. These are noted by a number, n, to describe the degree of rotation, the degree of translation is then added as a subscript showing how far along the axis the translation is, as a portion of the parallel lattice vector. So,21 is a rotation followed by a translation of 1/2 of the lattice vector
8.
Crystal structure
–
In crystallography, crystal structure is a description of the ordered arrangement of atoms, ions or molecules in a crystalline material. Ordered structures occur from the nature of the constituent particles to form symmetric patterns that repeat along the principal directions of three-dimensional space in matter. The smallest group of particles in the material that constitutes the pattern is the unit cell of the structure. The unit cell completely defines the symmetry and structure of the crystal lattice. The repeating patterns are said to be located at the points of the Bravais lattice, the lengths of the principal axes, or edges, of the unit cell and the angles between them are the lattice constants, also called lattice parameters. The symmetry properties of the crystal are described by the concept of space groups, all possible symmetric arrangements of particles in three-dimensional space may be described by the 230 space groups. The crystal structure and symmetry play a role in determining many physical properties, such as cleavage, electronic band structure. The crystal structure of a material can be described in terms of its unit cell, the unit cell is a box containing one or more atoms arranged in three dimensions. The unit cells stacked in three-dimensional space describe the arrangement of atoms of the crystal. Commonly, atomic positions are represented in terms of fractional coordinates, the atom positions within the unit cell can be calculated through application of symmetry operations to the asymmetric unit. The asymmetric unit refers to the smallest possible occupation of space within the unit cell and this does not, however imply that the entirety of the asymmetric unit must lie within the boundaries of the unit cell. Symmetric transformations of atom positions are calculated from the group of the crystal structure. Vectors and planes in a lattice are described by the three-value Miller index notation. It uses the indices ℓ, m, and n as directional parameters, which are separated by 90°, by definition, the syntax denotes a plane that intercepts the three points a1/ℓ, a2/m, and a3/n, or some multiple thereof. That is, the Miller indices are proportional to the inverses of the intercepts of the plane with the unit cell, if one or more of the indices is zero, it means that the planes do not intersect that axis. A plane containing a coordinate axis is translated so that it no longer contains that axis before its Miller indices are determined, the Miller indices for a plane are integers with no common factors. Negative indices are indicated with horizontal bars, as in, in an orthogonal coordinate system for a cubic cell, the Miller indices of a plane are the Cartesian components of a vector normal to the plane. Likewise, the planes are geometric planes linking nodes
9.
Crystal habit
–
In mineralogy, crystal habit is the characteristic external shape of an individual crystal or crystal group. A single crystals habit is a description of its shape and its crystallographic forms. Recognizing the habit may help in identifying a mineral, when the faces are well-developed due to uncrowded growth a crystal is called euhedral, one with partially developed faces is subhedral, and one with undeveloped crystal faces is called anhedral. The long axis of a quartz crystal typically has a six-sided prismatic habit with parallel opposite faces. Aggregates can be formed of individual crystals with euhedral to anhedral grains, the arrangement of crystals within the aggregate can be characteristic of certain minerals. For example, minerals used for asbestos insulation often grow in a fibrous habit, the terms used by mineralogists to report crystal habits describe the typical appearance of an ideal mineral. Recognizing the habit can aid in identification as some habits are characteristic, most minerals, however, do not display ideal habits due to conditions during crystallization. Minerals belonging to the crystal system do not necessarily exhibit the same habit. Some habits of a mineral are unique to its variety and locality, For example, while most sapphires form elongate barrel-shaped crystals, ordinarily, the latter habit is seen only in ruby. Sapphire and ruby are both varieties of the mineral, corundum. Some minerals may replace other existing minerals while preserving the originals habit, a classic example is tigers eye quartz, crocidolite asbestos replaced by silica. While quartz typically forms prismatic crystals, in tigers eye the original fibrous habit of crocidolite is preserved, the names of crystal habits are derived from, Predominant crystal faces. Abnormal grain growth Grain growth Crystallization
10.
Crystal
–
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
11.
Cleavage (crystal)
–
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
12.
Fracture (mineralogy)
–
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
13.
Conchoidal fracture
–
Conchoidal fracture describes the way that brittle materials break or fracture when they do not follow any natural planes of separation. Materials that break in this way include quartz, flint, quartzite, jasper and other fine-grained or amorphous materials with a composition of pure silica, such as obsidian, conchoidal fractures can also occur in other materials under favorable circumstances. This material property was used in the Stone Age to make sharp tools. Conchoidal fractures often result in a curved surface that resembles the rippling, gradual curves of a mussel shell. A swelling appears at the point of impact called the bulb of percussion, shock waves emanating outwards from this point leave their mark on the stone as ripples. Other conchoidal features include small fissures emanating from the bulb of percussion and this property also makes such fractures useful in engineering, since they provide a permanent record of the stress state at the time of failure. As conchoidal fractures can be produced only by mechanical impact, rather than frost cracking for example, the dictionary definition of conchoid at Wiktionary
14.
Mohs scale of mineral hardness
–
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
15.
Lustre (mineralogy)
–
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
16.
Streak (mineralogy)
–
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
17.
Transparency and translucency
–
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
18.
Specific gravity
–
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
19.
Refractive index
–
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
20.
Birefringence
–
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
21.
Ultraviolet
–
Ultraviolet is an electromagnetic radiation with a wavelength from 10 nm to 400 nm, shorter than that of visible light but longer than X-rays. UV radiation constitutes about 10% of the light output of the Sun. It is also produced by electric arcs and specialized lights, such as lamps, tanning lamps. Consequently, the effects of UV are greater than simple heating effects. Suntan, freckling and sunburn are familiar effects of over-exposure, along with risk of skin cancer. Living things on dry land would be damaged by ultraviolet radiation from the Sun if most of it were not filtered out by the Earths atmosphere. More-energetic, shorter-wavelength extreme UV below 121 nm ionizes air so strongly that it is absorbed before it reaches the ground, Ultraviolet is also responsible for the formation of bone-strengthening vitamin D in most land vertebrates, including humans. The UV spectrum thus has both beneficial and harmful to human health. Ultraviolet rays are invisible to most humans, the lens in a human eye ordinarily filters out UVB frequencies or higher, and humans lack color receptor adaptations for ultraviolet rays. Under some conditions, children and young adults can see ultraviolet down to wavelengths of about 310 nm, near-UV radiation is visible to some insects, mammals, and birds. Small birds have a fourth color receptor for ultraviolet rays, this gives birds true UV vision, reindeer use near-UV radiation to see polar bears, who are poorly visible in regular light because they blend in with the snow. UV also allows mammals to see urine trails, which is helpful for animals to find food in the wild. The males and females of some species look identical to the human eye. Ultraviolet means beyond violet, violet being the color of the highest frequencies of visible light, Ultraviolet has a higher frequency than violet light. He called them oxidizing rays to emphasize chemical reactivity and to them from heat rays. The terms chemical and heat rays were eventually dropped in favour of ultraviolet and infrared radiation, in 1878 the effect of short-wavelength light on sterilizing bacteria was discovered. By 1903 it was known the most effective wavelengths were around 250 nm, in 1960, the effect of ultraviolet radiation on DNA was established. The discovery of the ultraviolet radiation below 200 nm, named vacuum ultraviolet because it is absorbed by air, was made in 1893 by the German physicist Victor Schumann
22.
Fluorescence
–
Fluorescence is the emission of light by a substance that has absorbed light or other electromagnetic radiation. It is a form of luminescence, in most cases, the emitted light has a longer wavelength, and therefore lower energy, than the absorbed radiation. Fluorescent materials cease to glow immediately when the radiation source stops, unlike phosphorescence, Fluorescence also occurs frequently in nature in some minerals and in various biological states in many branches of the animal kingdom. An early observation of fluorescence was described in 1560 by Bernardino de Sahagún and it was derived from the wood of two tree species, Pterocarpus indicus and Eysenhardtia polystachya. The chemical compound responsible for this fluorescence is matlaline, which is the product of one of the flavonoids found in this wood. The name was derived from the fluorite, some examples of which contain traces of divalent europium. In a key experiment he used a prism to isolate ultraviolet radiation from sunlight, the specific frequencies of exciting and emitted light are dependent on the particular system. S0 is called the state of the fluorophore, and S1 is its first excited singlet state. A molecule in S1 can relax by various competing pathways and it can undergo non-radiative relaxation in which the excitation energy is dissipated as heat to the solvent. Excited organic molecules can also relax via conversion to a triplet state, relaxation from S1 can also occur through interaction with a second molecule through fluorescence quenching. Molecular oxygen is an extremely efficient quencher of fluorescence just because of its unusual triplet ground state, in most cases, the emitted light has a longer wavelength, and therefore lower energy, than the absorbed radiation, this phenomenon is known as the Stokes shift. The emitted radiation may also be of the wavelength as the absorbed radiation. Molecules that are excited through light absorption or via a different process can transfer energy to a second sensitized molecule, the fluorescence quantum yield gives the efficiency of the fluorescence process. It is defined as the ratio of the number of photons emitted to the number of photons absorbed, Φ = Number of photons emitted Number of photons absorbed The maximum fluorescence quantum yield is 1.0, each photon absorbed results in a photon emitted. Compounds with quantum yields of 0.10 are still considered quite fluorescent, thus, if the rate of any pathway changes, both the excited state lifetime and the fluorescence quantum yield will be affected. Fluorescence quantum yields are measured by comparison to a standard, the quinine salt quinine sulfate in a sulfuric acid solution is a common fluorescence standard. The fluorescence lifetime refers to the time the molecule stays in its excited state before emitting a photon. This is an instance of exponential decay, various radiative and non-radiative processes can de-populate the excited state
23.
Gemstone
–
A gemstone is a piece of mineral crystal which, in cut and polished form, is used to make jewelry or other adornments. However, certain rocks or organic materials that are not minerals are used for jewelry and are therefore often considered to be gemstones as well. Most gemstones are hard, but some soft minerals are used in jewelry because of their luster or other properties that have aesthetic value. Rarity is another characteristic that lends value to a gemstone, apart from jewelry, from earliest antiquity engraved gems and hardstone carvings, such as cups, were major luxury art forms. A gem maker is called a lapidary or gemcutter, a worker is a diamantaire. The carvings of Carl Fabergé are significant works in this tradition, the traditional classification in the West, which goes back to the ancient Greeks, begins with a distinction between precious and semi-precious, similar distinctions are made in other cultures. In modern usage the precious stones are diamond, ruby, sapphire, other stones are classified by their color, translucency and hardness. Another unscientific term for semi-precious gemstones used in art history and archaeology is hardstone, in modern times gemstones are identified by gemologists, who describe gems and their characteristics using technical terminology specific to the field of gemology. The first characteristic a gemologist uses to identify a gemstone is its chemical composition, for example, diamonds are made of carbon and rubies of aluminium oxide. Next, many gems are crystals which are classified by their crystal system such as cubic or trigonal or monoclinic, another term used is habit, the form the gem is usually found in. For example, diamonds, which have a crystal system, are often found as octahedrons. Gemstones are classified into different groups, species, and varieties, for example, ruby is the red variety of the species corundum, while any other color of corundum is considered sapphire. Other examples are the Emerald, aquamarine, red beryl, goshenite, heliodor, and morganite, gems are characterized in terms of refractive index, dispersion, specific gravity, hardness, cleavage, fracture, and luster. They may exhibit pleochroism or double refraction and they may have luminescence and a distinctive absorption spectrum. Material or flaws within a stone may be present as inclusions, gemstones may also be classified in terms of their water. This is a grading of the gems luster, transparency. Very transparent gems are considered first water, while second or third water gems are those of a lesser transparency, there is no universally accepted grading system for gemstones. Diamonds are graded using a system developed by the Gemological Institute of America in the early 1950s, historically, all gemstones were graded using the naked eye
24.
Mineral
–
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
25.
Green
–
Green is the color between blue and yellow on the spectrum of visible light. It is evoked by light with a predominant wavelength of roughly 495–570 nm, the modern English word green comes from the Middle English and Anglo-Saxon word grene, from the same Germanic root as the words grass and grow. It is the color of living grass and leaves and as a result is the color most associated with springtime, growth, by far the largest contributor to green in nature is chlorophyll, the chemical by which plants photosynthesize and convert sunlight into chemical energy. Many creatures have adapted to their environments by taking on a green hue themselves as camouflage. Several minerals have a color, including the emerald, which is colored green by its chromium content. In surveys made in Europe and the United States, green is the color most commonly associated with nature, life, health, youth, spring, hope and envy. In Europe and the U. S. green is associated with death, sickness, or the devil. In the Middle Ages and Renaissance, when the color of clothing showed the social status, green was worn by merchants, bankers. The Mona Lisa by Leonardo da Vinci wears green, showing she is not from a noble family, Green is also the traditional color of safety and permission, a green light means go ahead, a green card permits permanent residence in the United States. It is the most important color in Islam and it was the color of the banner of Muhammad, and is found in the flags of nearly all Islamic countries, and represents the lush vegetation of Paradise. It is also associated with the culture of Gaelic Ireland. Because of its association with nature, it is the color of the environmental movement, political groups advocating environmental protection and social justice describe themselves as part of the Green movement, some naming themselves Green parties. This has led to campaigns in advertising, as companies have sold green, or environmentally friendly. The word green comes from the Middle English and Old English word grene, which, like the German word grün, has the same root as the words grass and grow. It is from a Common Germanic *gronja-, which is reflected in Old Norse grænn, Old High German gruoni, ultimately from a PIE root *ghre- to grow. The first recorded use of the word as a term in Old English dates to ca. Latin with viridis also has a genuine and widely used term for green, related to virere to grow and ver spring, it gave rise to words in several Romance languages, French vert, Italian verde. Likewise the Slavic languages with zelenъ, Ancient Greek also had a term for yellowish, pale green – χλωρός, chloros, cognate with χλοερός verdant and χλόη the green of new growth
26.
Chromium
–
Chromium is a chemical element with symbol Cr and atomic number 24. It is the first element in Group 6 and it is a steely-grey, lustrous, hard and brittle metal which takes a high polish, resists tarnishing, and has a high melting point. The name of the element is derived from the Greek word χρῶμα, chrōma, meaning color, Chromium metal is of high value for its high corrosion resistance and hardness. A major development was the discovery that steel could be highly resistant to corrosion and discoloration by adding metallic chromium to form stainless steel. Stainless steel and chrome plating together comprise 85% of the commercial use, trivalent chromium ion is an essential nutrient in trace amounts in humans for insulin, sugar and lipid metabolism, although the issue is debated. While chromium metal and Cr ions are not considered toxic, hexavalent chromium is toxic and carcinogenic, abandoned chromium production sites often require environmental cleanup. Chromium is remarkable for its properties, it is the only elemental solid which shows antiferromagnetic ordering at room temperature. Above 38 °C, it changes to paramagnetic, Chromium metal left standing in air is passivated by oxidation, forming a thin, protective, surface layer. This layer is a structure only a few molecules thick. It is very dense, and prevents the diffusion of oxygen into the underlying metal and this is different from the oxide that forms on iron and carbon steel, through which elemental oxygen continues to migrate, reaching the underlying material to cause incessant rusting. Passivation can be enhanced by short contact with oxidizing acids like nitric acid, passivated chromium is stable against acids. Passivation can be removed with a reducing agent that destroys the protective oxide layer on the metal. Chromium metal treated in this way readily dissolves in weak acids, Chromium, unlike such metals as iron and nickel, does not suffer from hydrogen embrittlement. However, it suffer from nitrogen embrittlement, reacting with nitrogen from air. Chromium is the 22nd most abundant element in Earths crust with a concentration of 100 ppm. Chromium compounds are found in the environment from the erosion of chromium-containing rocks, Chromium is mined as chromite ore. About two-fifths of the ores and concentrates in the world are produced in South Africa, while Kazakhstan, India, Russia. Untapped chromite deposits are plentiful, but geographically concentrated in Kazakhstan, although rare, deposits of native chromium exist
27.
Vanadium
–
Vanadium is a chemical element with symbol V and atomic number 23. It is a hard, silvery grey, ductile, and malleable transition metal, the elemental metal is rarely found in nature, but once isolated artificially, the formation of an oxide layer stabilizes the free metal somewhat against further oxidation. Four years later, however, he was convinced by other scientists that erythronium was identical to chromium, both names were attributed to the wide range of colors found in vanadium compounds. Del Rios lead mineral was later renamed vanadinite for its vanadium content, in 1867 Henry Enfield Roscoe obtained the pure element. Vanadium occurs naturally in about 65 different minerals and in fossil fuel deposits and it is produced in China and Russia from steel smelter slag, other countries produce it either from the flue dust of heavy oil, or as a byproduct of uranium mining. It is mainly used to produce specialty steel alloys such as high-speed tool steels, the most important industrial vanadium compound, vanadium pentoxide, is used as a catalyst for the production of sulfuric acid. Large amounts of ions are found in a few organisms. The oxide and some salts of vanadium have moderate toxicity. Particularly in the ocean, vanadium is used by life forms as an active center of enzymes. Vanadium was discovered by Andrés Manuel del Río, a Spanish-Mexican mineralogist, Del Río extracted the element from a sample of Mexican brown lead ore, later named vanadinite. He found that its salts exhibit a variety of colors. Later, Del Río renamed the element erythronium because most of the salts turned red upon heating, Del Río accepted Collet-Descotils statement and retracted his claim. In 1831, the Swedish chemist Nils Gabriel Sefström rediscovered the element in a new oxide he found working with iron ores. Later that same year, Friedrich Wöhler confirmed del Ríos earlier work, Sefström chose a name beginning with V, which had not been assigned to any element yet. He called the element vanadium after Old Norse Vanadís, because of the many beautifully colored chemical compounds it produces, in 1831, the geologist George William Featherstonhaugh suggested that vanadium should be renamed rionium after del Río, but this suggestion was not followed. The isolation of vanadium metal proved difficult, in 1831, Berzelius reported the production of the metal, but Henry Enfield Roscoe showed that Berzelius had in fact produced the nitride, vanadium nitride. Roscoe eventually produced the metal in 1867 by reduction of chloride, VCl2. In 1927, pure vanadium was produced by reducing vanadium pentoxide with calcium, the first large-scale industrial use of vanadium was in the steel alloy chassis of the Ford Model T, inspired by French race cars
28.
Hardness
–
Hardness is a measure of how resistant solid matter is to various kinds of permanent shape change when a compressive force is applied. Some materials are harder than others, Hardness is dependent on ductility, elastic stiffness, plasticity, strain, strength, toughness, viscoelasticity, and viscosity. Common examples of matter are ceramics, concrete, certain metals, and superhard materials. There are three types of hardness measurements, scratch, indentation, and rebound. Within each of these classes of measurement there are individual measurement scales, for practical reasons conversion tables are used to convert between one scale and another. Scratch hardness is the measure of how resistant a sample is to fracture or permanent plastic deformation due to friction from a sharp object, the principle is that an object made of a harder material will scratch an object made of a softer material. When testing coatings, scratch hardness refers to the necessary to cut through the film to the substrate. The most common test is Mohs scale, which is used in mineralogy, one tool to make this measurement is the sclerometer. Another tool used to make these tests is the pocket hardness tester and this tool consists of a scale arm with graduated markings attached to a four-wheeled carriage. A scratch tool with a rim is mounted at a predetermined angle to the testing surface. In order to use it a weight of mass is added to the scale arm at one of the graduated markings. The use of the weight and markings allows a known pressure to be applied without the need for complicated machinery. Indentation hardness measures the resistance of a sample to material deformation due to a constant compression load from an object, they are primarily used in engineering. The tests work on the premise of measuring the critical dimensions of an indentation left by a specifically dimensioned and loaded indenter. Common indentation hardness scales are Rockwell, Vickers, Shore, rebound hardness, also known as dynamic hardness, measures the height of the bounce of a diamond-tipped hammer dropped from a fixed height onto a material. This type of hardness is related to elasticity, the device used to take this measurement is known as a scleroscope. Two scales that measures rebound hardness are the Leeb rebound hardness test, there are five hardening processes, Hall-Petch strengthening, work hardening, solid solution strengthening, precipitation hardening, and martensitic transformation. Hardness in the elastic range—a small temporary change in shape for a given force—is known as stiffness in the case of a given object and they exhibit plasticity—the ability to permanently change shape in response to the force, but remain in one piece
29.
Inclusion (mineral)
–
In mineralogy, an inclusion is any material that is trapped inside a mineral during its formation. In gemology, an inclusion is a characteristic enclosed within a gemstone, according to Huttons law of inclusions, fragments included in a host rock are older than the host rock itself. Inclusions are usually other minerals or rocks, but may also be water, liquid or vapor inclusions are known as fluid inclusions. In the case of amber it is possible to find insects and plants as inclusions, the analysis of atmospheric gas bubbles as inclusions in ice cores is an important tool in the study of climate change. A xenolith is a rock which has been picked up by a lava flow. Melt inclusions form when bits of melt become trapped inside crystals as they form in the melt, inclusions are one of the most important factors when it comes to gem valuation. In many gemstones, such as diamonds, inclusions affect the clarity of the gem, in some gems, however, such as star sapphires, the inclusion actually increases the value of the gem. Many colored gemstones, such as amethyst, emerald, and sapphire, are expected to have inclusions, colored gemstones are categorized into three types as follows, Type I colored gems include gems with very little or no inclusions. They include aquamarines, topaz and zircon, Type II colored gems include those that often have a few inclusions. They include sapphire, ruby, garnet and spinel, Type III colored gems include those that almost always have inclusions. Gems in this category include emerald and tourmaline, the term inclusion is also used in the context of metallurgy and metals processing. During the melt stage of processing hard particles such as oxides can enter or form in the metal which are subsequently trapped when the melt solidifies. The term is used negatively such as when the particle could act as a fatigue crack nucleator or as an area of high stress intensity
30.
Cyclosilicate
–
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
31.
Old French language
–
Old French was the Gallo-Romance dialect continuum spoken from the 9th century to the 14th century. In the 14th century, these came to be collectively known as the langues doïl. The mid-14th century is taken as the period to Middle French. The areal of Old French in contemporary terms corresponded to the parts of the Kingdom of France, Upper Burgundy. As part of the emerging Gallo-Romance dialect continuum, the langues doïl were contrasted with the langue doc, in these examples, we notice a clear consequence of bilingualism, that sometimes even changed the first syllable of the Latin words. Pope estimated that perhaps still 15% of the vocabulary of modern French derives from Germanic sources, at the third Council of Tours in 813, priests were ordered to preach in the vernacular language, since the common people could no longer understand formal Latin. The second-oldest document in Old French is the Eulalia sequence, which is important for reconstruction of Old French pronunciation due to its consistent spelling. The Capetians langue doïl, the forerunner of modern standard French, did not begin to become the common speech of all of France, however, until after the French Revolution. In the Late Middle Ages, the Old French dialects diverged into a number of distinct langues doïl, during the Early Modern period, French now becomes established as the official language of the Kingdom of France throughout the realm, also including the langue doc-speaking territories in the south. Old French gives way to Middle French in the mid-14th century, the earliest extant French literary texts date from the ninth century, but very few texts before the 11th century have survived. The first literary works written in Old French were saints lives, the Canticle of Saint Eulalie, written in the second half of the 9th century, is generally accepted as the first such text. The first of these is the area of the chansons de geste. More than one hundred chansons de geste have survived in three hundred manuscripts. The oldest and most celebrated of the chansons de geste is The Song of Roland, a fourth grouping, not listed by Bertrand, is the Crusade cycle, dealing with the First Crusade and its immediate aftermath. Jean Bodels other two categories—the Matter of Rome and the Matter of Britain—concern the French romance or roman, around a hundred verse romances survive from the period 1150–1220. From around 1200 on, the tendency was increasingly to write the romances in prose, the most important romance of the 13th century is the Romance of the Rose which breaks considerably from the conventions of the chivalric adventure story. The Occitan or Provençal poets were called troubadours, from the word trobar to find, lyric poets in Old French are called trouvères. By the late 13th century, the tradition in France had begun to develop in ways that differed significantly from the troubadour poets
32.
Middle English
–
This stage of the development of the English language roughly followed the High to the Late Middle Ages. Middle English developed out of Late Old English, seeing many dramatic changes in its grammar, pronunciation and this largely forms the basis for Modern English spelling, although pronunciation has changed considerably since that time. Middle English was succeeded in England by the era of Early Modern English, by that time, a variant of the Northumbrian dialect was developing into the Scots language. During the Middle English period many Old English grammatical features were simplified or disappeared, noun, adjective and verb inflections were simplified, a process that included the reduction of most grammatical case distinctions. Middle English also saw an adoption of Norman French vocabulary, especially in areas such as politics, law. Everyday English vocabulary remained mostly Germanic, with Old Norse influence becoming apparent, significant changes in pronunciation took place, especially for long vowels and diphthongs, which in the later Middle English period began to undergo the Great Vowel Shift. Little survives of early Middle English literature, most likely due to the Norman domination, poets wrote both in the vernacular and courtly English. It is popularly believed that William Shakespeare wrote in Middle English, the latter part of the 11th century was a period of transition from Late Old English to Early Middle English. The influence of Old Norse certainly helped move English from a synthetic language towards a more analytic or isolating word order and it was, after all, a salutary influence. The gain was greater than the loss, there was a gain in directness, in clarity, and in strength. The change to Old English from Old Norse was substantive, pervasive and it is most important to recognise that in many words the English and Scandinavian language differed chiefly in their inflectional elements. The body of the word was so nearly the same in the two languages only the endings would put obstacles in the way of mutual understanding. In the mixed population which existed in the Danelaw these endings must have led to confusion, tending gradually to become obscured. This blending of peoples and languages resulted in simplifying English grammar. There are also many Norman-derived terms relating to the cultures that arose in the 12th century. Sometimes, and particularly later, words were taken from Latin, giving such sets as kingly, later French borrowings came from standard rather than Norman French, this leads to such cognate pairs as warden, guardian. The end of Anglo-Saxon rule did not, of course, change the language immediately, the general population would have spoken the same dialects as before the Conquest, these changed slowly until written records of them became available for study, which varies in different regions. Once the writing of Old English came to an end, Middle English had no standard language, Early Middle English has a largely Anglo-Saxon vocabulary, but a greatly simplified inflectional system
33.
Vulgar Latin
–
Vulgar Latin or Sermo Vulgaris is a generic term for the nonstandard sociolects of Latin from which the Romance languages developed. Works written in Latin during classical times used Classical Latin rather than Vulgar Latin, because of its nonstandard nature, Vulgar Latin had no official orthography. Vulgar Latin is sometimes also called colloquial Latin, or Common Romance, in Renaissance Latin, Vulgar Latin was called vulgare Latinum or Latinum vulgare. The term common speech, which later became Vulgar Latin, was used by inhabitants of the Roman Empire, traces of their language appear in some inscriptions, such as graffiti or advertisements. The educated population mainly responsible for Classical Latin might also have spoken Vulgar Latin in certain contexts depending on their socioeconomic background, the term was first used improperly in that sense by the pioneers of Romance-language philology, François Juste Marie Raynouard and Friedrich Christian Diez. These terms, as he points out later in the work, are a translation into German of Dantes vulgare latinum and Latinum vulgare, and these names in turn are at the end of a tradition extending to the Roman republic. Latin could be sermo Latinus, but in addition was a variety known as sermo vulgaris, sermo vulgi, sermo plebeius and these modifiers inform post-classical readers that a conversational Latin existed, which was used by the masses in daily speaking and was perceived as lower-class. These vocabulary items manifest no opposition to the written language, there was an opposition to higher-class, or family Latin in sermo familiaris and very rarely literature might be termed sermo nobilis. The supposed sermo classicus is a scholarly fiction unattested in the dictionary, all kinds of sermo were spoken only, not written. If one wanted to refer to what in post-classical times was called classical Latin one resorted to the concept of latinitas or latine. If one spoke in the lingua or sermo Latinus one merely spoke Latin, but if one spoke latine or latinius one spoke good Latin, and formal Latin had latinitas, the original opposition was between formal or implied good Latin and informal or Vulgar Latin. The spoken/written dichotomy is entirely philological, although making it clear that sermo vulgaris existed, the ancients said very little about it. Because it was not transcribed, it can only be studied indirectly, knowledge comes from these chief sources, Solecisms, especially in Late Latin texts. Mention of it by ancient grammarians, including prescriptive grammar texts from the Late Latin period condemning linguistic errors that represent spoken Latin, the comparative method, which reconstructs Proto-Romance, a hypothetical vernacular proto-language from which the Romance languages descended. The original written Latin language was adapted from the spoken language of the Latins, with some minor modifications. As with many languages, over time the spoken language diverged from the written language with the written language remaining somewhat static. Nevertheless, during the period spoken Latin still remained largely common across the Empire. The collapse of the Western Roman Empire rapidly began to change this, the former western provinces became increasingly isolated from the Eastern Roman Empire leading to a rapid divergence in the Latin spoken on either side
34.
Latin
–
Latin is a classical language belonging to the Italic branch of the Indo-European languages. The Latin alphabet is derived from the Etruscan and Greek alphabets, Latin was originally spoken in Latium, in the Italian Peninsula. Through the power of the Roman Republic, it became the dominant language, Vulgar Latin developed into the Romance languages, such as Italian, Portuguese, Spanish, French, and Romanian. Latin, Italian and French have contributed many words to the English language, Latin and Ancient Greek roots are used in theology, biology, and medicine. By the late Roman Republic, Old Latin had been standardised into Classical Latin, Vulgar Latin was the colloquial form spoken during the same time and attested in inscriptions and the works of comic playwrights like Plautus and Terence. Late Latin is the language from the 3rd century. Later, Early Modern Latin and Modern Latin evolved, Latin was used as the language of international communication, scholarship, and science until well into the 18th century, when it began to be supplanted by vernaculars. Ecclesiastical Latin remains the language of the Holy See and the Roman Rite of the Catholic Church. Today, many students, scholars and members of the Catholic clergy speak Latin fluently and it is taught in primary, secondary and postsecondary educational institutions around the world. The language has been passed down through various forms, some inscriptions have been published in an internationally agreed, monumental, multivolume series, the Corpus Inscriptionum Latinarum. Authors and publishers vary, but the format is about the same, volumes detailing inscriptions with a critical apparatus stating the provenance, the reading and interpretation of these inscriptions is the subject matter of the field of epigraphy. The works of several hundred ancient authors who wrote in Latin have survived in whole or in part and they are in part the subject matter of the field of classics. The Cat in the Hat, and a book of fairy tales, additional resources include phrasebooks and resources for rendering everyday phrases and concepts into Latin, such as Meissners Latin Phrasebook. The Latin influence in English has been significant at all stages of its insular development. From the 16th to the 18th centuries, English writers cobbled together huge numbers of new words from Latin and Greek words, dubbed inkhorn terms, as if they had spilled from a pot of ink. Many of these words were used once by the author and then forgotten, many of the most common polysyllabic English words are of Latin origin through the medium of Old French. Romance words make respectively 59%, 20% and 14% of English, German and those figures can rise dramatically when only non-compound and non-derived words are included. Accordingly, Romance words make roughly 35% of the vocabulary of Dutch, Roman engineering had the same effect on scientific terminology as a whole
35.
Ancient Greek
–
Ancient Greek includes the forms of Greek used in ancient Greece and the ancient world from around the 9th century BC to the 6th century AD. It is often divided into the Archaic period, Classical period. It is antedated in the second millennium BC by Mycenaean Greek, the language of the Hellenistic phase is known as Koine. Koine is regarded as a historical stage of its own, although in its earliest form it closely resembled Attic Greek. Prior to the Koine period, Greek of the classic and earlier periods included several regional dialects, Ancient Greek was the language of Homer and of fifth-century Athenian historians, playwrights, and philosophers. It has contributed many words to English vocabulary and has been a subject of study in educational institutions of the Western world since the Renaissance. This article primarily contains information about the Epic and Classical phases of the language, Ancient Greek was a pluricentric language, divided into many dialects. The main dialect groups are Attic and Ionic, Aeolic, Arcadocypriot, some dialects are found in standardized literary forms used in literature, while others are attested only in inscriptions. There are also several historical forms, homeric Greek is a literary form of Archaic Greek used in the epic poems, the Iliad and Odyssey, and in later poems by other authors. Homeric Greek had significant differences in grammar and pronunciation from Classical Attic, the origins, early form and development of the Hellenic language family are not well understood because of a lack of contemporaneous evidence. Several theories exist about what Hellenic dialect groups may have existed between the divergence of early Greek-like speech from the common Proto-Indo-European language and the Classical period and they have the same general outline, but differ in some of the detail. The invasion would not be Dorian unless the invaders had some relationship to the historical Dorians. The invasion is known to have displaced population to the later Attic-Ionic regions, the Greeks of this period believed there were three major divisions of all Greek people—Dorians, Aeolians, and Ionians, each with their own defining and distinctive dialects. Often non-west is called East Greek, Arcadocypriot apparently descended more closely from the Mycenaean Greek of the Bronze Age. Boeotian had come under a strong Northwest Greek influence, and can in some respects be considered a transitional dialect, thessalian likewise had come under Northwest Greek influence, though to a lesser degree. Most of the dialect sub-groups listed above had further subdivisions, generally equivalent to a city-state and its surrounding territory, Doric notably had several intermediate divisions as well, into Island Doric, Southern Peloponnesus Doric, and Northern Peloponnesus Doric. The Lesbian dialect was Aeolic Greek and this dialect slowly replaced most of the older dialects, although Doric dialect has survived in the Tsakonian language, which is spoken in the region of modern Sparta. Doric has also passed down its aorist terminations into most verbs of Demotic Greek, by about the 6th century AD, the Koine had slowly metamorphosized into Medieval Greek
36.
Hue
–
Orange and violet are the other hues, for a total of six, as in the rainbow, red, orange, yellow, green, blue, violet. The other color appearance parameters are colorfulness, chroma, saturation, lightness, usually, colors with the same hue are distinguished with adjectives referring to their lightness and/or colorfulness, such as with light blue, pastel blue, vivid blue. Exceptions include brown, which is a dark orange, in painting color theory, a hue refers to a pure color—one without tint or shade. A hue is an element of the color wheel, hues are first processed in the brain in areas in the extended V4 called globs. Hue is the component of the polar representation, while chroma is the radial component. Specifically, in CIELAB h a b = a t a n 2, while, analogously, in CIELUV h u v = a t a n 2 = a t a n 2, where, atan2 is a two-argument inverse tangent. Preucil describes a color hexagon, similar to a trilinear plot described by Evans, Hanson, and Brewer, to place red at 0°, green at 120°, and blue at 240°, h r g b = a t a n 2. Equivalently, one may solve tan =3 ⋅2 ⋅ R − G − B, Preucil used a polar plot, which he termed a color circle. Using R, G, and B, one may compute hue angle using the scheme, determine which of the six possible orderings of R, G. Note that in case the formula contains the fraction M − L H − L, where H is the highest of R, G, and B, L is the lowest. This is referred to as the Preucil hue error and was used in the computation of mask strength in photomechanical color reproduction, the formulae used are those in the table above. The hues exhibited by caramel colorings and beers are fairly limited in range, the Linner hue index is used to quantify the hue of such products. Replacements are often used for chromium, cadmium and alizarin, dominant wavelength is a physical analog to the perceptual attribute hue. On a chromaticity diagram, a line is drawn from a point through the coordinates of the color in question. There are two ways in which hue difference is quantified. The first is the difference between the two hue angles. The symbol for expression of hue difference is Δ h a b in CIELAB. The other is computed as the total color difference after Lightness and Chroma differences have been accounted for, its symbol is Δ H a b ∗ in CIELAB
37.
Colorfulness
–
Colorfulness or saturation in colorimetry and color theory refers to the perceived intensity of a specific color. Colorfulness is the visual sensation according to which the color of an area appears to be more or less chromatic. Chroma is the relative to the brightness of a similarly illuminated area that appears to be white or highly transmitting. Therefore, chroma should not be confused with colorfulness, saturation is the colorfulness of a color relative to its own brightness. A highly colorful stimulus is vivid and intense, while a less colorful stimulus appears more muted, with no colorfulness at all, a color is a “neutral” gray. Any color can be described using three color appearance parameters — colorfulness, lightness, and hue, saturation is one of three coordinates in the HSL and HSV color spaces. The saturation of a color is determined by a combination of light intensity, the purest color is achieved by using just one wavelength at a high intensity, such as in laser light. If the intensity drops, then as a result the saturation drops, to desaturate a color of given intensity in a subtractive system, one can add white, black, gray, or the hues complement. CIELUV The chroma normalized by the lightness, s u v = C u v ∗ L ∗ =132 +2 where is the chromaticity of the white point, and chroma is defined below. Nevertheless, this provides a reasonable predictor of saturation. S a b = C a b ∗ C a b ∗2 + L ∗2100 % where Sab is the saturation, L* the lightness and C*ab is the chroma of the color. CIECAM02 The square root of the colorfulness divided by the brightness, M is proportional to the chroma C, thus the CIECAM02 definition bears some similarity to the CIELUV definition. An important difference is that the CIECAM02 model accounts for the conditions through the parameter FL. Different color spaces, such as CIELAB or CIELUV may be used, the naïve definition of saturation does not specify its response function. However, both color spaces are nonlinear in terms of perceived color differences. It is also possible—and sometimes desirable—to define a quantity that is linearized in term of the psychovisual perception. The transformation of to is given by, C a b ∗ = a ∗2 + b ∗2 h a b = arctan b ∗ a ∗ and analogously for CIE L*C*h. The chroma in the CIE L*C*h and CIE L*C*h coordinates has the advantage of being more psychovisually linear, and therefore, chroma in CIE1976 L*a*b* and L*u*v* color spaces is very much different from the traditional sense of saturation
38.
Lightness
–
In colorimetry and color theory, lightness, also known as value or tone, is a representation of variation in the perception of a color or color spaces brightness. It is one of the color appearance parameters of any color appearance model, various color models have an explicit term for this property. The Munsell color model uses the value, while the HSL color model, HCL color space. The HSV model uses the value a little differently, a color with a low value is nearly black. In subtractive color value changes can be achieved by adding black or white to the color, chiaroscuro and Tenebrism both take advantage of dramatic contrasts of value to heighten drama in art. Artists may also employ shading, subtle manipulation of value, the Munsell value has long been used as a perceptually uniform lightness scale. A question of interest is the relationship between the Munsell value scale and the relative luminance, aware of the Weber–Fechner law, Munsell remarked Should we use a logarithmic curve or curve of squares. The remainder of section is a chronology of lightness approximations. – Munsells V runs from 0 to 10, while Y typically runs from 0 to 100, typically, the relative luminance is normalized so that the reference white has a tristimulus value of Y =100. Since the reflectance of magnesium oxide relative to the perfect reflecting diffuser is 97. 5%,1943 Newhall, Nickerson, and Judd prepare a report for the Optical Society of America. They suggest a quintic parabola, Y =1.221,9 V −0.231,11 V2 +0.239,51 V3 −0.021,009 V4 +0.000,840,4 V5. 1943 Using Table II of the O. S. A, report, Moon and Spencer express the value in terms of the relative luminance, V =50.426 =1.4 Y0.426. 1944 Saunderson and Milner introduce a constant in the previous expression. Later, Jameson and Hurvich claim that this corrects for simultaneous contrast effects, V =2.357 Y0.343 −1.52. 1955 Ladd and Pinney of Eastman Kodak are interested in the Munsell value as a uniform lightness scale for use in television. After considering one logarithmic and five power-law functions, they relate value to reflectance by raising the reflectance to the power of 0.352, V =2.217 Y0.352 −1.324. Realizing this is close to the cube root, they simplify it to. 1958 Glasser et al. define the lightness as ten times the Munsell value,1964 Wyszecki simplifies this to, W ⋆ =25 Y1 /3 −17
39.
Loupe
–
A loupe is a simple, small magnification device used to see small details more closely. Loupes are also called hand lenses, three basic types of loupes exist, Simple lenses, generally used for low-magnification designs because of high optical aberration. Compound lenses, generally used for higher magnifications to control optical aberration, loupes are used in a number of industries, notably the jewelry trade, watchmaking, photography, printing, dentistry, education and ophthalmology. Loupes are also used in academia and life sciences, such as geology and biology, amateur naturalists may also find a hand lens or a loupe a useful tool when looking at or identifying species. They are also used in numismatics and stamp collecting, jewelers typically use a monocular, handheld loupe in order to magnify gemstones and other jewelry that they wish to inspect. A 10× magnification is good to use for inspecting jewelry and hallmarks and is the Gemological Institute of Americas standard for grading diamond clarity. Stones will sometimes be inspected at higher magnifications than 10×, although the depth of field, the accepted standard for grading diamonds is therefore that inclusions and blemishes visible at 10× impact the clarity grade. Loupes are employed to assist watchmakers in assembling mechanical watches, typical magnifications for viewing slides full-frame depend on image format,35 mm frames are best viewn at ca. 5×, while ca. 3× is optimal for viewing medium format slides, often, a 10× loupe is used to examine critical sharpness. Photographers using large format cameras use a loupe to view the ground glass image to aid in focusing. DSLR camera users also use loupes to help to identify dust and other particles on the sensor, offset and flexographic printing see frequent use of loupes in order to carefully analyze how ink lies on paper. Strippers use loupes in order to register film separations to one another, pressmen use them to check registration of colors, estimate dot-gain, and diagnose issues with roller pressure and chemistry based on the shape of individual dots and rosettes. Dental loupes aid dentists, hygienists, and dental therapists to devise accurate diagnose of oral conditions, additionally, loupes can improve dentists posture which can decrease occupational strain. Dental caries, also known as cavities, are most accurately identified by visual and tactile examination of a clean, magnification enables dentists to improve their ability to differentiate between a stain and a cavity. Cavities are rated and scored based on their visual presentation, if magnification is too high diagnosis becomes difficult due to the small field of view. Ideal magnification for diagnostic purposes is up to 2×, treatment of dental caries, periodontal disease, and pulpal disease are aided by magnification. The dental specialty of endodontics has performed the vast majority of research regarding magnification in dentistry, treatment of periodontal disease is achieved by removing calculus deposits, plaque and therefore bacteria which causes inflammation and subsequently bone destruction. In severe cases, surgery to reduce pocket depth is indicated, periodontists and hygienists must visualize plaque and calculus to remove it
40.
Cabochon
–
A cabochon, from the Middle French word caboche, is a gemstone which has been shaped and polished as opposed to faceted. The resulting form is usually a convex obverse with a flat reverse, cutting en cabochon is usually applied to opaque gems, while faceting is usually applied to transparent stones. Hardness is also taken into account as softer gemstones with a lower than 7 on the Mohs hardness scale are easily scratched, mainly by silicon dioxide in dust. This would quickly make translucent gems unattractive—instead they are polished as cabochons, the usual shape for cutting cabochons is an ellipse. An exception is cabochons on some watches crowns, which are round, the procedure is to cut a slab of the rough rock with a slab saw, and next to stencil a shape from a template. The slab is then trimmed near the line using a diamond blade saw—called a trim saw. Diamond impregnated wheels or silicon carbide wheels can be used to grind the rock down. Most lapidary workshops and production facilities have moved away from silicon carbide to diamond grinding wheels or flat lap disks, once the piece is trimmed it can be dopped or completed by hand. Dopping is normally done by adhering the stone with hard wax onto a length of wooden dowel called a dop stick, the piece is then ground to the template line, the back edges may be bevelled, and finally the top is sanded and polished to a uniform dome
41.
Lapidary
–
A lapidary is an artist or artisan who forms stone, minerals, or gemstones into decorative items such as cabochons, engraved gems, including cameos, and faceted designs. The primary techniques employed are cutting, grinding, and polishing, carving is an important, but specialised technique. Hardstone carving is the used in art history for objects produced by the specialised carving techniques. Diamond cutters are not referred to as lapidaries, due to the specialized techniques which are required to work diamond. By extension the term lapidary has sometimes applied to collectors of and dealer in gems. The etymological roots of lapidary is in the Latin word lapis which means stone, the term evolved from lapidarius meaning stonecutter or working with stone, into Old French lapidaire, thereon to mean one skilled in working with precious stones in 14th century. These powers included the belief in the ability of stones to prevent harm, the word appeared as an English adjective in the 18th century. The earliest known lapidary work likely occurred during the Stone Age, as people created tools from stone, they inevitably realized that some geological materials were harder than others. The next earliest documented examples of one may consider to be lapidary arts came in the form of drilling stone. The earliest roots of drilling rocks, a method, date back to approximately one million years ago. The early Egyptians developed cutting and jewelry fashioning methods for lapis lazuli, turquoise, the lapidary arts were quite well developed in the Indian subcontinent by early 1st millennium CE. They discuss sources of gems and diamonds, their origins, qualities, several other Sanskrit texts on gems and lapidary, have been dated to post-10th century suggesting a continuous lapidary practice. According to Jason Hawkes and Stephanie Wynne-Jones, archaeological evidence suggests that trade between Africa and India, in products from lapidary arts, was established in the 1st millennium CE, lapidary has been a significant tradition in early Mesoamerica. These were made from shell, jade, turquoise and greenstones, the lapidary products were used as a status symbol, offerings and during burials. The Aztec used string saw, reed and bone drills for their lapidary arts, apart from figurative carving, there are three broad categories of lapidary arts. These are the procedures of tumbling, cabochon cutting, and faceting, most modern lapidary work is done using motorized equipment. Polishing is done with resin or metal bonded emery, silicon carbide, in older systems the grinding and polishing powders were applied separately to the grinding or buffing wheel. Often, the final polish will use a different medium, such as tin oxide or cerium oxide, cutting of harder stones is done with a diamond tipped saw
42.
Cedar oil
–
Cedar oil, also known as cedarwood oil, is an essential oil derived from various types of conifers, most in the pine or cypress botanical families. It is produced from the foliage, and sometimes the wood, roots, although termed cedar or cedarwood oils, the most important oils are produced from distilling wood of a number of different junipers and cypresses, rather than true cedars. Similar oils are distilled, pressed or chemically extracted in small quantities from wood, roots, and leaves from plants of the genera Platycladus, Cupressus, Taiwania, and Calocedrus. The cedarwood oil of the ancients, in particular the Sumerians and Egyptians, was derived from the Cedar of Lebanon, the once-mighty Cedar of Lebanon forests of antiquity have been almost entirely eradicated, and today no commercial oil extraction is based on this species. One of the found in many cedar trees is cedrol. Depending on the amount of cedrol in a species of cedar can determine its pesticidal effect on insects. Ancient Egyptians would use the oil from trees in the embalming process. Cedarwood oils each have characteristic woody odours which may change somewhat in the course of drying out, the crude oils are often yellowish or even darker in color and some, such as Texas cedarwood oil, are quite viscous and deposit crystals on standing. They find use in a range of applications such as soap perfumes, household sprays. Small quantities are used in work as a clearing oil. All the cedarwood oils of commerce contain a group of related compounds. The oils are used both directly and as sources of chemical isolates. Cedarwood oil was used as the base for paints by the ancient Sumerians and they would grind cobalt compounds in a mortar and pestle to produce a blue pigment. They could obtain green from copper, yellow from lead antimonate, black from charcoal, today, cedarwood oil is often used for its aromatic properties, especially in aromatherapy, it can also be used to renew the smell of natural cedar furniture. Cedarwood oil is used as a repellent, both directly applied to the skin and as an additive to sprays, candles and other products. In India, oil from the deodar cedar has been shown to possess insecticidal and antifungal properties, one of three methods of ancient Egyptian embalming practices employs the use of cedarwood oil. This was a less costly method than the most well known of the ancient Egyptian practices of removing internal organs for separate preservation in canopic jars, the practice. called for the injection of cedar oil into body cavities without evisceration. Until the development of synthetic immersion oil in the 1940s, cedarwood oil was used for the oil immersion objective in light microscopy
43.
Federal Trade Commission
–
The Federal Trade Commission is an independent agency of the United States government, established in 1914 by the Federal Trade Commission Act. Its principal mission is the promotion of consumer protection and the elimination and prevention of anticompetitive business practices, the Federal Trade Commission Act was one of President Woodrow Wilsons major acts against trusts. Trusts and trust-busting were significant political concerns during the Progressive Era. Since its inception, the FTC has enforced the provisions of the Clayton Act, over time, the FTC has been delegated with the enforcement of additional business regulation statutes and has promulgated a number of regulations. He would make the first speech on the House floor advocating its creation on February 21,1912, though the initial bill did not pass, the questions of trusts and antitrust dominated the 1912 election. With the 1912 presidential election decided in favor of the Democrats and Woodrow Wilson, the national debate culminated in Wilsons signing of the FTC Act on September 26, with additional tightening of regulations in the Clayton Antitrust Act three weeks later. The new Federal Trade Commission would absorb the staff and duties of Bureau of Corporations, previously established under the Department of Commerce, the following table lists commissioners as of March 2017. Recent former commissioners were, The Bureau of Consumer Protections mandate is to protect consumers against unfair or deceptive acts or practices in commerce, with the written consent of the Commission, Bureau attorneys enforce federal laws related to consumer affairs and rules promulgated by the FTC. Its functions include investigations, enforcement actions, and consumer and business education, areas of principal concern for this bureau are, advertising and marketing, financial products and practices, telemarketing fraud, privacy and identity protection, etc. The bureau also is responsible for the United States National Do Not Call Registry, under the FTC Act, the Commission has the authority, in most cases, to bring its actions in federal court through its own attorneys. In some consumer protection matters, the FTC appears with, or supports, the Bureau of Competition is the division of the FTC charged with elimination and prevention of anticompetitive business practices. It accomplishes this through the enforcement of antitrust laws, review of proposed mergers, the FTC shares enforcement of antitrust laws with the Department of Justice. The FTC investigates issues raised by reports from consumers and businesses, pre-merger notification filings, congressional inquiries and these issues include, for instance, false advertising and other forms of fraud. FTC investigations may pertain to a company or an entire industry. Traditionally an administrative complaint is heard in front of an independent administrative law judge with FTC staff acting as prosecutors. The case is reviewed de novo by the full FTC commission which then may be appealed to the U. S. Court of Appeals, in numerous cases, the FTC employs this authority to combat serious consumer deception or fraud. Additionally, the FTC has rulemaking power to address concerns regarding industry-wide practices, Rules promulgated under this authority are known as Trade Rules. In the mid-1990s, the FTC launched the fraud sweeps concept where the agency and its federal, state, the first sweeps operation was Project Telesweep in July 1995 which cracked down on 100 business opportunity scams
44.
Trapiche emerald
–
Trapiche emerald is a rare variety of the gemstone emerald, characterized by a six-pointed radial pattern of ray-like spokes of dark impurities. It is one of several types of trapiche or trapiche-like minerals, the name comes from the Spanish term trapiche, a sugar mill, because of the resemblance of the pattern to the spokes of a grinding wheel. Trapiche emeralds were first described by Émile Bertrand in 1879 and they are generally only found in the western part of the Eastern Cordillera basin, in the Muzo, Coscuez and Peñas Blancas mines of Colombia. Singular finds in Brazil and Madagascar have also been reported, the radial pattern exhibits considerable variance, and often includes a hexagonal structure at the core. There is not yet consensus about the mechanism by which the pattern forms, according to Isabella Pignatelli et al. the black impurities are remains of the shale matrix in which the emeralds formed, trapped between the radial dendrites of the growing emerald. The trapiche pattern is not an asterism, a similar pattern that forms in a different process
45.
Ancient Egypt
–
Ancient Egypt was a civilization of ancient Northeastern Africa, concentrated along the lower reaches of the Nile River in what is now the modern country of Egypt. It is one of six civilizations to arise independently, Egyptian civilization followed prehistoric Egypt and coalesced around 3150 BC with the political unification of Upper and Lower Egypt under the first pharaoh Narmer. In the aftermath of Alexander the Greats death, one of his generals, Ptolemy Soter and this Greek Ptolemaic Kingdom ruled Egypt until 30 BC, when, under Cleopatra, it fell to the Roman Empire and became a Roman province. The success of ancient Egyptian civilization came partly from its ability to adapt to the conditions of the Nile River valley for agriculture, the predictable flooding and controlled irrigation of the fertile valley produced surplus crops, which supported a more dense population, and social development and culture. Its art and architecture were widely copied, and its antiquities carried off to far corners of the world and its monumental ruins have inspired the imaginations of travelers and writers for centuries. The Nile has been the lifeline of its region for much of human history, nomadic modern human hunter-gatherers began living in the Nile valley through the end of the Middle Pleistocene some 120,000 years ago. By the late Paleolithic period, the climate of Northern Africa became increasingly hot and dry. In Predynastic and Early Dynastic times, the Egyptian climate was less arid than it is today. Large regions of Egypt were covered in treed savanna and traversed by herds of grazing ungulates, foliage and fauna were far more prolific in all environs and the Nile region supported large populations of waterfowl. Hunting would have been common for Egyptians, and this is also the period when many animals were first domesticated. The largest of these cultures in upper Egypt was the Badari, which probably originated in the Western Desert, it was known for its high quality ceramics, stone tools. The Badari was followed by the Amratian and Gerzeh cultures, which brought a number of technological improvements, as early as the Naqada I Period, predynastic Egyptians imported obsidian from Ethiopia, used to shape blades and other objects from flakes. In Naqada II times, early evidence exists of contact with the Near East, particularly Canaan, establishing a power center at Hierakonpolis, and later at Abydos, Naqada III leaders expanded their control of Egypt northwards along the Nile. They also traded with Nubia to the south, the oases of the desert to the west. Royal Nubian burials at Qustul produced artifacts bearing the oldest-known examples of Egyptian dynastic symbols, such as the crown of Egypt. They also developed a ceramic glaze known as faience, which was used well into the Roman Period to decorate cups, amulets, and figurines. During the last predynastic phase, the Naqada culture began using written symbols that eventually were developed into a system of hieroglyphs for writing the ancient Egyptian language. The Early Dynastic Period was approximately contemporary to the early Sumerian-Akkadian civilisation of Mesopotamia, the third-century BC Egyptian priest Manetho grouped the long line of pharaohs from Menes to his own time into 30 dynasties, a system still used today
_2.jpg)
.jpg)
_-2.jpg)
