1.
Nesosilicate
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Silicate minerals are rock-forming minerals made up of silicate groups. They are the largest and most important class of rock-forming minerals and they are classified based on the structure of their silicate groups, which contain different ratios of silicon and oxygen. Nesosilicates, or orthosilicates, have the orthosilicate ion, which constitute isolated 4− tetrahedra that are connected only by interstitial cations and these exist as 3-member 6− and 6-member 12− rings, where T stands for a tetrahedrally coordinated cation. Inosilicates, or chain silicates, have interlocking chains of silicate tetrahedra with either SiO3,1,3 ratio, for single chains or Si4O11,4,11 ratio, for double chains. Nickel–Strunz classification,09. D Pyroxene group Enstatite – orthoferrosilite series Enstatite – MgSiO3 Ferrosilite – FeSiO3 Pigeonite – Ca0.251, all phyllosilicate minerals are hydrated, with either water or hydroxyl groups attached. Serpentine subgroup Antigorite – Mg3Si2O54 Chrysotile – Mg3Si2O54 Lizardite – Mg3Si2O54 Clay minerals group Halloysite – Al2Si2O54 Kaolinite – Al2Si2O54 Illite – 24O10 Montmorillonite –0 and this group comprises nearly 75% of the crust of the Earth. Tectosilicates, with the exception of the group, are aluminosilicates. Nickel–Strunz classification,09. F and 09. G,04. A, an introduction to the rock-forming minerals. Wise, W. S. Zussman, J. Rock-forming minerals, P.982 pp. Hurlbut, Cornelius S. Danas Manual of Mineralogy. Mindat. org, Dana classification Webmineral, Danas New Silicate Classification Media related to Silicates at Wikimedia Commons
2.
Chemical formula
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These are limited to a single typographic line of symbols, which may include subscripts and superscripts. A chemical formula is not a name, and it contains no words. Although a chemical formula may imply certain simple chemical structures, it is not the same as a full chemical structural formula. Chemical formulas can fully specify the structure of only the simplest of molecules and chemical substances, the simplest types of chemical formulas are called empirical formulas, which use letters and numbers indicating the numerical proportions of atoms of each type. Molecular formulas indicate the numbers of each type of atom in a molecule. For example, the formula for glucose is CH2O, while its molecular formula is C6H12O6. This is possible if the relevant bonding is easy to show in one dimension, an example is the condensed molecular/chemical formula for ethanol, which is CH3-CH2-OH or CH3CH2OH. For reasons of structural complexity, there is no condensed chemical formula that specifies glucose, chemical formulas may be used in chemical equations to describe chemical reactions and other chemical transformations, such as the dissolving of ionic compounds into solution. A chemical formula identifies each constituent element by its chemical symbol, in empirical formulas, these proportions begin with a key element and then assign numbers of atoms of the other elements in the compound, as ratios to the key element. For molecular compounds, these numbers can all be expressed as whole numbers. For example, the formula of ethanol may be written C2H6O because the molecules of ethanol all contain two carbon atoms, six hydrogen atoms, and one oxygen atom. Some types of compounds, however, cannot be written with entirely whole-number empirical formulas. An example is boron carbide, whose formula of CBn is a variable non-whole number ratio with n ranging from over 4 to more than 6.5. When the chemical compound of the consists of simple molecules. These types of formulas are known as molecular formulas and condensed formulas. A molecular formula enumerates the number of atoms to reflect those in the molecule, so that the formula for glucose is C6H12O6 rather than the glucose empirical formula. However, except for very simple substances, molecular chemical formulas lack needed structural information, for simple molecules, a condensed formula is a type of chemical formula that may fully imply a correct structural formula. For example, ethanol may be represented by the chemical formula CH3CH2OH
3.
Crystal system
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In crystallography, the terms crystal system, crystal family and lattice system each refer to one of several classes of space groups, lattices, point groups or crystals. Informally, two crystals are in the crystal system if they have similar symmetries, though there are many exceptions to this. Space groups and crystals are divided into seven crystal systems according to their point groups, five of the crystal systems are essentially the same as five of the lattice systems, but the hexagonal and trigonal crystal systems differ from the hexagonal and rhombohedral lattice systems. The six crystal families are formed by combining the hexagonal and trigonal crystal systems into one hexagonal family, a lattice system is a class of lattices with the same set of lattice point groups, which are subgroups of the arithmetic crystal classes. The 14 Bravais lattices are grouped into seven lattice systems, triclinic, monoclinic, orthorhombic, tetragonal, rhombohedral, hexagonal, in a crystal system, a set of point groups and their corresponding space groups are assigned to a lattice system. Of the 32 point groups that exist in three dimensions, most are assigned to only one system, in which case both the crystal and lattice systems have the same name. However, five point groups are assigned to two systems, rhombohedral and hexagonal, because both exhibit threefold rotational symmetry. These point groups are assigned to the crystal system. In total there are seven crystal systems, triclinic, monoclinic, orthorhombic, tetragonal, trigonal, hexagonal, a crystal family is determined by lattices and point groups. It is formed by combining crystal systems which have space groups assigned to a lattice system. In three dimensions, the families and systems are identical, except the hexagonal and trigonal crystal systems. In total there are six families, triclinic, monoclinic, orthorhombic, tetragonal, hexagonal. Spaces with less than three dimensions have the number of crystal systems, crystal families and lattice systems. In one-dimensional space, there is one crystal system, in 2D space, there are four crystal systems, oblique, rectangular, square and hexagonal. The relation between three-dimensional crystal families, crystal systems and lattice systems is shown in the table, Note. To avoid confusion of terminology, the term trigonal lattice is not used, if the original structure and inverted structure are identical, then the structure is centrosymmetric. Still, even for non-centrosymmetric case, inverted structure in some cases can be rotated to align with the original structure and this is the case of non-centrosymmetric achiral structure. If the inverted structure cannot be rotated to align with the structure, then the structure is chiral
4.
Orthorhombic crystal system
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In crystallography, the orthorhombic crystal system is one of the 7 crystal systems. All three bases intersect at 90° angles, so the three lattice vectors remain mutually orthogonal, there are two orthorhombic Bravais lattices in two dimensions, Primitive rectangular and centered rectangular. The primitive rectangular lattice can also be described by a centered rhombic unit cell, there are four orthorhombic Bravais lattices, primitive orthorhombic, base-centered orthorhombic, body-centered orthorhombic, and face-centered orthorhombic. In this axis setting, the primitive and base-centered lattices interchange in centering type, crystal structure Overview of all space groups Hurlbut, Cornelius S. Klein, Cornelis. Hahn, Theo, ed. International Tables for Crystallography, Volume A, Space Group Symmetry
5.
Crystal habit
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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
6.
Cleavage (crystal)
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Cleavage, in mineralogy, is the tendency of crystalline materials to split along definite crystallographic structural planes. Cleavage forms parallel to planes, Basal or pinacoidal cleavage occurs when there is only one cleavage plane. Mica also has basal cleavage, this is why mica can be peeled into thin sheets, cubic cleavage occurs on when there are three cleavage planes intersecting at 90 degrees. Halite has cubic cleavage, and therefore, when halite crystals are broken, octahedral cleavage occurs when there are four cleavage planes in a crystal. Octahedral cleavage is common for semiconductors, rhombohedral cleavage occurs when there are three cleavage planes intersecting at angles that are not 90 degrees. Prismatic cleavage occurs when there are two planes in a crystal. Dodecahedral cleavage occurs when there are six cleavage planes in a crystal, crystal parting occurs when minerals break along planes of structural weakness due to external stress or along twin composition planes. Parting breaks are very similar in appearance to cleavage, but only due to stress. Examples include magnetite which shows octahedral parting, the parting of corundum. Cleavage is a property traditionally used in mineral identification, both in hand specimen and microscopic examination of rock and mineral studies. As an example, the angles between the cleavage planes for the pyroxenes and the amphiboles are diagnostic. Crystal cleavage is of importance in the electronics industry and in the cutting of gemstones. Precious stones are generally cleaved by impact, as in diamond cutting, synthetic single crystals of semiconductor materials are generally sold as thin wafers which are much easier to cleave. Elemental semiconductors are diamond cubic, a group for which octahedral cleavage is observed. This means that some orientations of wafer allow near-perfect rectangles to be cleaved, most other commercial semiconductors can be made in the related zinc blende structure, with similar cleavage planes. Cleavage Mineral galleries, Mineral properties – Cleavage
7.
Fracture (mineralogy)
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In the field of mineralogy, fracture is the texture and shape of a rocks surface formed when a mineral is fractured. Minerals often have a highly distinctive fracture, making it a feature used in their identification. Fracture differs from cleavage in that the latter involves clean splitting along the planes of the minerals crystal structure. All minerals exhibit fracture, but when very strong cleavage is present, conchoidal fracture breakage that resembles the concentric ripples of a mussel shell. It often occurs in amorphous or fine-grained minerals such as flint, opal or obsidian, subconchoidal fracture is similar to conchoidal fracture, but with less significant curvature. Earthy fracture is reminiscent of freshly broken soil and it is frequently seen in relatively soft, loosely bound minerals, such as limonite, kaolinite and aluminite. Hackly fracture is jagged, sharp and not even and it occurs when metals are torn, and so is often encountered in native metals such as copper and silver. Splintery fracture comprises sharp elongated points and it is particularly seen in fibrous minerals such as chrysotile, but may also occur in non-fibrous minerals such as kyanite. Uneven fracture is a surface or one with random irregularities. It occurs in a range of minerals including arsenopyrite, pyrite and magnetite. Rudolf Duda and Lubos Rejl, Minerals of the World http, //www. galleries. com/minerals/property/fracture. htm
8.
Conchoidal fracture
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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
9.
Mohs scale of mineral hardness
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The Mohs scale of mineral hardness is a qualitative ordinal scale characterizing scratch resistance of various minerals through the ability of harder material to scratch softer material. Created in 1812 by German geologist and mineralogist Friedrich Mohs, it is one of several definitions of hardness in materials science, while greatly facilitating the identification of minerals in the field, the Mohs scale does not show how well hard materials perform in an industrial setting. Despite its lack of precision, the Mohs scale is highly relevant for field geologists, the Mohs scale hardness of minerals can be commonly found in reference sheets. Reference materials may be expected to have a uniform Mohs hardness, the Mohs scale of mineral hardness is based on the ability of one natural sample of mineral to scratch another mineral visibly. The samples of matter used by Mohs are all different minerals, Minerals are pure substances found in nature. Rocks are made up of one or more minerals, as the hardest known naturally occurring substance when the scale was designed, diamonds are at the top of the scale. The hardness of a material is measured against the scale by finding the hardest material that the material can scratch. For example, if material is scratched by apatite but not by fluorite. Scratching a material for the purposes of the Mohs scale means creating non-elastic dislocations visible to the naked eye, frequently, materials that are lower on the Mohs scale can create microscopic, non-elastic dislocations on materials that have a higher Mohs number. The Mohs scale is an ordinal scale. For example, corundum is twice as hard as topaz, the table below shows the comparison with the absolute hardness measured by a sclerometer, with pictorial examples. On the Mohs scale, a streak plate has a hardness of 7.0, using these ordinary materials of known hardness can be a simple way to approximate the position of a mineral on the scale. The table below incorporates additional substances that may fall between levels, Comparison between Hardness and Hardness, Mohs hardness of elements is taken from G. V, samsonov in Handbook of the physicochemical properties of the elements, IFI-Plenum, New York, USA,1968. The Hardness of Minerals and Rocks
10.
Lustre (mineralogy)
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Lustre or luster is the way light interacts with the surface of a crystal, rock, or mineral. The word traces its origins back to the latin lux, meaning light, a range of terms are used to describe lustre, such as earthy, metallic, greasy, and silky. Similarly, the term refers to a glassy lustre. A list of terms is given below. Lustre varies over a continuum, and so there are no rigid boundaries between the different types of lustre. The terms are frequently combined to describe types of lustre. Some minerals exhibit unusual optical phenomena, such as asterism or chatoyancy, a list of such phenomena is given below. Adamantine minerals possess a superlative lustre, which is most notably seen in diamond, such minerals are transparent or translucent, and have a high refractive index. Minerals with an adamantine lustre are uncommon, with examples being cerussite. Minerals with a degree of lustre are referred to as subadamantine, with some examples being garnet. Dull minerals exhibit little to no lustre, due to coarse granulations which scatter light in all directions, a distinction is sometimes drawn between dull minerals and earthy minerals, with the latter being coarser, and having even less lustre. Greasy minerals resemble fat or grease, a greasy lustre often occurs in minerals containing a great abundance of microscopic inclusions, with examples including opal and cordierite. Many minerals with a greasy lustre also feel greasy to the touch, metallic minerals have the lustre of polished metal, and with ideal surfaces will work as a reflective surface. Examples include galena, pyrite and magnetite, pearly minerals consist of thin transparent co-planar sheets. Light reflecting from these layers give them a lustre reminiscent of pearls, such minerals possess perfect cleavage, with examples including muscovite and stilbite. Resinous minerals have the appearance of resin, chewing gum or plastic, a principal example is amber, which is a form of fossilized resin. Silky minerals have an arrangement of extremely fine fibres, giving them a lustre reminiscent of silk. Examples include asbestos, ulexite and the satin spar variety of gypsum, a fibrous lustre is similar, but has a coarser texture
11.
Streak (mineralogy)
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The streak of a mineral is the color of the powder produced when it is dragged across an un-weathered surface. If no streak seems to be made, the streak is said to be white or colorless. Streak is particularly important as a diagnostic for opaque and colored materials and it is less useful for silicate minerals, most of which have a white streak or are too hard to powder easily. The apparent color of a mineral can vary widely because of impurities or a disturbed macroscopic crystal structure. Small amounts of an impurity that strongly absorbs a particular wavelength can radically change the wavelengths of light that are reflected by the specimen, and thus change the apparent color. However, when the specimen is dragged to produce a streak, it is broken into randomly oriented microscopic crystals, the surface across which the mineral is dragged is called a streak plate, and is generally made of unglazed porcelain tile. In the absence of a plate, the unglazed underside of a porcelain bowl or vase or the back of a glazed tile will work. Sometimes a streak is more easily or accurately described by comparing it with the streak made by another streak plate. Because the trail left behind results from the mineral being crushed into powder, in case of harder minerals, the color of the powder can be determined by filing or crushing with a hammer a small sample, which is then usually rubbed on a streak plate. Most minerals that are harder have a white streak. Some minerals leave a similar to their natural color, such as cinnabar. Other minerals leave surprising colors, such as fluorite, which always has a streak, although it can appear in purple, blue, yellow. Hematite, which is black in appearance, leaves a red streak which accounts for its name, galena, which can be similar in appearance to hematite, is easily distinguished by its gray streak. Hamilton, W. R. Cambridge Guide to Minerals, Rocks, the Encyclopedia of Gemstones and Minerals. New York, Facts on File. p.251, physical Characteristics of Minerals, at Introduction to Mineralogy by Andrea Bangert What is Streak
12.
Transparency and translucency
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In the field of optics, transparency is the physical property of allowing light to pass through the material without being scattered. On a macroscopic scale, the photons can be said to follow Snells Law, in other words, a translucent medium allows the transport of light while a transparent medium not only allows the transport of light but allows for image formation. The opposite property of translucency is opacity, transparent materials appear clear, with the overall appearance of one color, or any combination leading up to a brilliant spectrum of every color. When light encounters a material, it can interact with it in different ways. These interactions depend on the wavelength of the light and the nature of the material, photons interact with an object by some combination of reflection, absorption and transmission. Some materials, such as glass and clean water, transmit much of the light that falls on them and reflect little of it. Many liquids and aqueous solutions are highly transparent, absence of structural defects and molecular structure of most liquids are mostly responsible for excellent optical transmission. Materials which do not transmit light are called opaque, many such substances have a chemical composition which includes what are referred to as absorption centers. Many substances are selective in their absorption of light frequencies. They absorb certain portions of the spectrum while reflecting others. The frequencies of the spectrum which are not absorbed are either reflected or transmitted for our physical observation and this is what gives rise to color. The attenuation of light of all frequencies and wavelengths is due to the mechanisms of absorption. Transparency can provide almost perfect camouflage for animals able to achieve it and this is easier in dimly-lit or turbid seawater than in good illumination. Many marine animals such as jellyfish are highly transparent, at the atomic or molecular level, physical absorption in the infrared portion of the spectrum depends on the frequencies of atomic or molecular vibrations or chemical bonds, and on selection rules. Nitrogen and oxygen are not greenhouse gases because there is no absorption because there is no molecular dipole moment. With regard to the scattering of light, the most critical factor is the scale of any or all of these structural features relative to the wavelength of the light being scattered. Primary material considerations include, Crystalline structure, whether or not the atoms or molecules exhibit the long-range order evidenced in crystalline solids, glassy structure, scattering centers include fluctuations in density or composition. Microstructure, scattering centers include internal surfaces such as boundaries, crystallographic defects
13.
Specific gravity
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This page is about the measurement using water as a reference. For a general use of gravity, see relative density. See intensive property for the property implied by specific, Apparent specific gravity is the ratio of the weight of a volume of the substance to the weight of an equal volume of the reference substance. The reference substance is always water at its densest for liquids. Nonetheless, the temperature and pressure must be specified for both the sample and the reference, pressure is nearly always 1 atm. Temperatures for both sample and reference vary from industry to industry, in British beer brewing, the practice for specific gravity as specified above is to multiply it by 1000. Being a ratio of densities, specific gravity is a dimensionless quantity, Specific gravity varies with temperature and pressure, reference and sample must be compared at the same temperature and pressure or be corrected to a standard reference temperature and pressure. Substances with a gravity of 1 are neutrally buoyant in water. Those with SG greater than 1 are denser than water and will, disregarding surface tension effects and those with an SG less than 1 are less dense than water and will float on it. In scientific work, the relationship of mass to volume is expressed directly in terms of the density of the substance under study. It is in industry where specific gravity finds wide application, often for historical reasons. True specific gravity can be expressed mathematically as, S G true = ρ sample ρ H2 O where ρ sample is the density of the sample, the density of water varies with temperature and pressure as does the density of the sample. So it is necessary to specify the temperatures and pressures at which the densities or weights were determined and it is nearly always the case that measurements are made at 1 nominal atmosphere. For true specific gravity calculations, air pressure must be considered, temperatures are specified by the notation with T s representing the temperature at which the samples density was determined and T r the temperature at which the reference density is specified. For example, SG would be understood to mean that the density of the sample was determined at 20°C and of the water at 4°C. Taking into account different sample and reference temperatures, we note that, while S G H2 O =1.000000, it is also the case that S G H2 O =0.998203 /0.999840 =0.998363. Here, temperature is being specified using the current ITS-90 scale, on the previous IPTS-68 scale, the densities at 20 °C and 4 °C are 0.9982071 and 0.9999720 respectively, resulting in an SG value for water of 0.9982343. For example, in the industry, the Plato table lists sucrose concentration by weight against true SG
14.
Refractive index
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In optics, the refractive index or index of refraction n of a material is a dimensionless number that describes how light propagates through that medium. It is defined as n = c v, where c is the speed of light in vacuum, for example, the refractive index of water is 1.333, meaning that light travels 1.333 times faster in a vacuum than it does in water. The refractive index determines how light is bent, or refracted. The refractive indices also determine the amount of light that is reflected when reaching the interface, as well as the angle for total internal reflection. This implies that vacuum has a index of 1. The refractive index varies with the wavelength of light and this is called dispersion and causes the splitting of white light into its constituent colors in prisms and rainbows, and chromatic aberration in lenses. Light propagation in absorbing materials can be described using a refractive index. The imaginary part then handles the attenuation, while the real part accounts for refraction, the concept of refractive index is widely used within the full electromagnetic spectrum, from X-rays to radio waves. It can also be used with wave phenomena such as sound, in this case the speed of sound is used instead of that of light and a reference medium other than vacuum must be chosen. Thomas Young was presumably the person who first used, and invented, at the same time he changed this value of refractive power into a single number, instead of the traditional ratio of two numbers. The ratio had the disadvantage of different appearances, newton, who called it the proportion of the sines of incidence and refraction, wrote it as a ratio of two numbers, like 529 to 396. Hauksbee, who called it the ratio of refraction, wrote it as a ratio with a fixed numerator, hutton wrote it as a ratio with a fixed denominator, like 1.3358 to 1. Young did not use a symbol for the index of refraction, in the next years, others started using different symbols, n, m, and µ. For visible light most transparent media have refractive indices between 1 and 2, a few examples are given in the adjacent table. These values are measured at the yellow doublet D-line of sodium, with a wavelength of 589 nanometers, gases at atmospheric pressure have refractive indices close to 1 because of their low density. Almost all solids and liquids have refractive indices above 1.3, aerogel is a very low density solid that can be produced with refractive index in the range from 1.002 to 1.265. Moissanite lies at the end of the range with a refractive index as high as 2.65. Most plastics have refractive indices in the range from 1.3 to 1.7, for infrared light refractive indices can be considerably higher
15.
Birefringence
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Birefringence is the optical property of a material having a refractive index that depends on the polarization and propagation direction of light. These optically anisotropic materials are said to be birefringent, the birefringence is often quantified as the maximum difference between refractive indices exhibited by the material. Crystals with non-cubic crystal structures are often birefringent, as are plastics under mechanical stress and this effect was first described by the Danish scientist Rasmus Bartholin in 1669, who observed it in calcite, a crystal having one of the strongest birefringences. A mathematical description of wave propagation in a birefringent medium is presented below, following is a qualitative explanation of the phenomenon. Thus rotating the material around this axis does not change its optical behavior and this special direction is known as the optic axis of the material. Light whose polarization is perpendicular to the axis is governed by a refractive index no. Light whose polarization is in the direction of the optic axis sees an optical index ne, for any ray direction there is a linear polarization direction perpendicular to the optic axis, and this is called an ordinary ray. The magnitude of the difference is quantified by the birefringence, Δ n = n e − n o, the propagation of the ordinary ray is simply described by no as if there were no birefringence involved. However the extraordinary ray, as its name suggests, propagates unlike any wave in an optical material. Its refraction at a surface can be using the effective refractive index. However it is in fact an inhomogeneous wave whose power flow is not exactly in the direction of the wave vector and this causes an additional shift in that beam, even when launched at normal incidence, as is popularly observed using a crystal of calcite as photographed above. Rotating the calcite crystal will cause one of the two images, that of the ray, to rotate slightly around that of the ordinary ray. When the light propagates either along or orthogonal to the optic axis, in the first case, both polarizations see the same effective refractive index, so there is no extraordinary ray. In the second case the extraordinary ray propagates at a different phase velocity but is not an inhomogeneous wave, for instance, a quarter-wave plate is commonly used to create circular polarization from a linearly polarized source. The case of so-called biaxial crystals is substantially more complex and these are characterized by three refractive indices corresponding to three principal axes of the crystal. For most ray directions, both polarizations would be classified as extraordinary rays but with different effective refractive indices, being extraordinary waves, however, the direction of power flow is not identical to the direction of the wave vector in either case. The two refractive indices can be determined using the index ellipsoids for given directions of the polarization, note that for biaxial crystals the index ellipsoid will not be an ellipsoid of revolution but is described by three unequal principle refractive indices nα, nβ and nγ. Thus there is no axis around which a rotation leaves the optical properties invariant, for this reason, birefringent materials with three distinct refractive indices are called biaxial
16.
Mineral
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A mineral is a naturally occurring chemical compound, usually of crystalline form and abiogenic in origin. A mineral has one specific chemical composition, whereas a rock can be an aggregate of different minerals or mineraloids, the study of minerals is called mineralogy. There are over 5,300 known mineral species, over 5,070 of these have been approved by the International Mineralogical Association, the silicate minerals compose over 90% of the Earths crust. The diversity and abundance of species is controlled by the Earths chemistry. Silicon and oxygen constitute approximately 75% of the Earths crust, which translates directly into the predominance of silicate minerals, minerals are distinguished by various chemical and physical properties. Differences in chemical composition and crystal structure distinguish the various species, changes in the temperature, pressure, or bulk composition of a rock mass cause changes in its minerals. Minerals can be described by their various properties, which are related to their chemical structure. Common distinguishing characteristics include crystal structure and habit, hardness, lustre, diaphaneity, colour, streak, tenacity, cleavage, fracture, parting, more specific tests for describing minerals include magnetism, taste or smell, radioactivity and reaction to acid. Minerals are classified by key chemical constituents, the two dominant systems are the Dana classification and the Strunz classification, the silicate class of minerals is subdivided into six subclasses by the degree of polymerization in the chemical structure. All silicate minerals have a unit of a 4− silica tetrahedron—that is, a silicon cation coordinated by four oxygen anions. These tetrahedra can be polymerized to give the subclasses, orthosilicates, disilicates, cyclosilicates, inosilicates, phyllosilicates, other important mineral groups include the native elements, sulfides, oxides, halides, carbonates, sulfates, and phosphates. The first criterion means that a mineral has to form by a natural process, stability at room temperature, in the simplest sense, is synonymous to the mineral being solid. More specifically, a compound has to be stable or metastable at 25 °C, modern advances have included extensive study of liquid crystals, which also extensively involve mineralogy. Minerals are chemical compounds, and as such they can be described by fixed or a variable formula, many mineral groups and species are composed of a solid solution, pure substances are not usually found because of contamination or chemical substitution. Finally, the requirement of an ordered atomic arrangement is usually synonymous with crystallinity, however, crystals are also periodic, an ordered atomic arrangement gives rise to a variety of macroscopic physical properties, such as crystal form, hardness, and cleavage. There have been recent proposals to amend the definition to consider biogenic or amorphous substances as minerals. The formal definition of an approved by the IMA in 1995, A mineral is an element or chemical compound that is normally crystalline. However, if geological processes were involved in the genesis of the compound, Mineral classification schemes and their definitions are evolving to match recent advances in mineral science
17.
Magnesium
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Magnesium is a chemical element with symbol Mg and atomic number 12. Magnesium is the ninth most abundant element in the universe and it is produced in large, aging stars from the sequential addition of three helium nuclei to a carbon nucleus. When such stars explode as supernovas, much of the magnesium is expelled into the medium where it may recycle into new star systems. Magnesium is the eighth most abundant element in the Earths crust and the fourth most common element in the Earth, making up 13% of the planets mass and it is the third most abundant element dissolved in seawater, after sodium and chlorine. Magnesium occurs naturally only in combination with elements, where it invariably has a +2 oxidation state. The free element can be produced artificially, and is highly reactive, the free metal burns with a characteristic brilliant-white light. The metal is now obtained mainly by electrolysis of magnesium salts obtained from brine, Magnesium is less dense than aluminium, and the alloy is prized for its combination of lightness and strength. Magnesium is the eleventh most abundant element by mass in the body and is essential to all cells. Magnesium ions interact with polyphosphate compounds such as ATP, DNA, hundreds of enzymes require magnesium ions to function. Magnesium compounds are used medicinally as common laxatives, antacids, elemental magnesium is a gray-white lightweight metal, two-thirds the density of aluminium. Magnesium has the lowest melting and the lowest boiling point 1,363 K of all the alkaline earth metals, Magnesium reacts with water at room temperature, though it reacts much more slowly than calcium, a similar group 2 metal. When submerged in water, hydrogen bubbles form slowly on the surface of the metal—though, if powdered, the reaction occurs faster with higher temperatures. Magnesiums reversible reaction with water can be harnessed to store energy, Magnesium also reacts exothermically with most acids such as hydrochloric acid, producing the metal chloride and hydrogen gas, similar to the HCl reaction with aluminium, zinc, and many other metals. Magnesium is highly flammable, especially when powdered or shaved into thin strips, flame temperatures of magnesium and magnesium alloys can reach 3,100 °C, although flame height above the burning metal is usually less than 300 mm. Once ignited, such fires are difficult to extinguish, with combustion continuing in nitrogen, carbon dioxide, Magnesium may also be used as an igniter for thermite, a mixture of aluminium and iron oxide powder that ignites only at a very high temperature. When burning in air, magnesium produces a light that includes strong ultraviolet wavelengths. Magnesium powder was used for illumination in the early days of photography. Later, magnesium filament was used in electrically ignited single-use photography flashbulbs, Magnesium powder is used in fireworks and marine flares where a brilliant white light is required
18.
Iron
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Iron is a chemical element with symbol Fe and atomic number 26. It is a metal in the first transition series and it is by mass the most common element on Earth, forming much of Earths outer and inner core. It is the fourth most common element in the Earths crust, like the other group 8 elements, ruthenium and osmium, iron exists in a wide range of oxidation states, −2 to +6, although +2 and +3 are the most common. Elemental iron occurs in meteoroids and other low oxygen environments, but is reactive to oxygen, fresh iron surfaces appear lustrous silvery-gray, but oxidize in normal air to give hydrated iron oxides, commonly known as rust. Unlike the metals that form passivating oxide layers, iron oxides occupy more volume than the metal and thus flake off, Iron metal has been used since ancient times, although copper alloys, which have lower melting temperatures, were used even earlier in human history. Pure iron is soft, but is unobtainable by smelting because it is significantly hardened and strengthened by impurities, in particular carbon. A certain proportion of carbon steel, which may be up to 1000 times harder than pure iron. Crude iron metal is produced in blast furnaces, where ore is reduced by coke to pig iron, further refinement with oxygen reduces the carbon content to the correct proportion to make steel. Steels and iron alloys formed with metals are by far the most common industrial metals because they have a great range of desirable properties. Iron chemical compounds have many uses, Iron oxide mixed with aluminium powder can be ignited to create a thermite reaction, used in welding and purifying ores. Iron forms binary compounds with the halogens and the chalcogens, among its organometallic compounds is ferrocene, the first sandwich compound discovered. Iron plays an important role in biology, forming complexes with oxygen in hemoglobin and myoglobin. Iron is also the metal at the site of many important redox enzymes dealing with cellular respiration and oxidation and reduction in plants. A human male of average height has about 4 grams of iron in his body and this iron is distributed throughout the body in hemoglobin, tissues, muscles, bone marrow, blood proteins, enzymes, ferritin, hemosiderin, and transport in plasma. The mechanical properties of iron and its alloys can be evaluated using a variety of tests, including the Brinell test, Rockwell test, the data on iron is so consistent that it is often used to calibrate measurements or to compare tests. An increase in the content will cause a significant increase in the hardness. Maximum hardness of 65 Rc is achieved with a 0. 6% carbon content, because of the softness of iron, it is much easier to work with than its heavier congeners ruthenium and osmium. Because of its significance for planetary cores, the properties of iron at high pressures and temperatures have also been studied extensively
19.
Silicate minerals
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Silicate minerals are rock-forming minerals made up of silicate groups. They are the largest and most important class of rock-forming minerals and they are classified based on the structure of their silicate groups, which contain different ratios of silicon and oxygen. Nesosilicates, or orthosilicates, have the orthosilicate ion, which constitute isolated 4− tetrahedra that are connected only by interstitial cations and these exist as 3-member 6− and 6-member 12− rings, where T stands for a tetrahedrally coordinated cation. Inosilicates, or chain silicates, have interlocking chains of silicate tetrahedra with either SiO3,1,3 ratio, for single chains or Si4O11,4,11 ratio, for double chains. Nickel–Strunz classification,09. D Pyroxene group Enstatite – orthoferrosilite series Enstatite – MgSiO3 Ferrosilite – FeSiO3 Pigeonite – Ca0.251, all phyllosilicate minerals are hydrated, with either water or hydroxyl groups attached. Serpentine subgroup Antigorite – Mg3Si2O54 Chrysotile – Mg3Si2O54 Lizardite – Mg3Si2O54 Clay minerals group Halloysite – Al2Si2O54 Kaolinite – Al2Si2O54 Illite – 24O10 Montmorillonite –0 and this group comprises nearly 75% of the crust of the Earth. Tectosilicates, with the exception of the group, are aluminosilicates. Nickel–Strunz classification,09. F and 09. G,04. A, an introduction to the rock-forming minerals. Wise, W. S. Zussman, J. Rock-forming minerals, P.982 pp. Hurlbut, Cornelius S. Danas Manual of Mineralogy. Mindat. org, Dana classification Webmineral, Danas New Silicate Classification Media related to Silicates at Wikimedia Commons
20.
Silicon
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Silicon is a chemical element with symbol Si and atomic number 14. A hard and brittle crystalline solid with a metallic luster. It is a member of group 14 in the table, along with carbon above it and germanium, tin, lead. It is not very reactive, although more reactive than germanium, Silicon is the eighth most common element in the universe by mass, but very rarely occurs as the pure element in the Earths crust. It is most widely distributed in dusts, sands, planetoids, over 90% of the Earths crust is composed of silicate minerals, making silicon the second most abundant element in the Earths crust after oxygen. Most silicon is used commercially without being separated, and often with little processing of the natural minerals, such use includes industrial construction with clays, silica sand, and stone. Silicate is used in Portland cement for mortar and stucco, and mixed with sand and gravel to make concrete for walkways, foundations. Silicates are used in whiteware ceramics such as porcelain, and in traditional quartz-based soda-lime glass, Silicon compounds such as silicon carbide are used as abrasives and components of high-strength ceramics. Elemental silicon also has an impact on the modern world economy. Most free silicon is used in the refining, aluminium-casting. Silicon is the basis of the widely used synthetic polymers called silicones, Silicon is an essential element in biology, although only tiny traces are required by animals. However, various sea sponges and microorganisms, such as diatoms and radiolaria, silica is deposited in many plant tissues, such as in the bark and wood of Chrysobalanaceae and the silica cells and silicified trichomes of Cannabis sativa, horsetails and many grasses. Silicon is a solid at room temperature, with a point of 1,414 °C. Like water, it has a density in a liquid state than in a solid state and it expands when it freezes. With a relatively high conductivity of 149 W·m−1·K−1, silicon conducts heat well. In its crystalline form, pure silicon has a gray color, like germanium, silicon is rather strong, very brittle, and prone to chipping. Silicon, like carbon and germanium, crystallizes in a cubic crystal structure with a lattice spacing of 0.5430710 nm. The outer electron orbital of silicon, like that of carbon, has four valence electrons, the 1s, 2s, 2p and 3s subshells are completely filled while the 3p subshell contains two electrons out of a possible six
21.
Oxygen
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Oxygen is a chemical element with symbol O and atomic number 8. It is a member of the group on the periodic table and is a highly reactive nonmetal. By mass, oxygen is the third-most abundant element in the universe, after hydrogen, at standard temperature and pressure, two atoms of the element bind to form dioxygen, a colorless and odorless diatomic gas with the formula O2. This is an important part of the atmosphere and diatomic oxygen gas constitutes 20. 8% of the Earths atmosphere, additionally, as oxides the element makes up almost half of the Earths crust. Most of the mass of living organisms is oxygen as a component of water, conversely, oxygen is continuously replenished by photosynthesis, which uses the energy of sunlight to produce oxygen from water and carbon dioxide. Oxygen is too reactive to remain a free element in air without being continuously replenished by the photosynthetic action of living organisms. Another form of oxygen, ozone, strongly absorbs ultraviolet UVB radiation, but ozone is a pollutant near the surface where it is a by-product of smog. At low earth orbit altitudes, sufficient atomic oxygen is present to cause corrosion of spacecraft, the name oxygen was coined in 1777 by Antoine Lavoisier, whose experiments with oxygen helped to discredit the then-popular phlogiston theory of combustion and corrosion. One of the first known experiments on the relationship between combustion and air was conducted by the 2nd century BCE Greek writer on mechanics, Philo of Byzantium. In his work Pneumatica, Philo observed that inverting a vessel over a burning candle, Philo incorrectly surmised that parts of the air in the vessel were converted into the classical element fire and thus were able to escape through pores in the glass. Many centuries later Leonardo da Vinci built on Philos work by observing that a portion of air is consumed during combustion and respiration, Oxygen was discovered by the Polish alchemist Sendivogius, who considered it the philosophers stone. In the late 17th century, Robert Boyle proved that air is necessary for combustion, English chemist John Mayow refined this work by showing that fire requires only a part of air that he called spiritus nitroaereus. From this he surmised that nitroaereus is consumed in both respiration and combustion, Mayow observed that antimony increased in weight when heated, and inferred that the nitroaereus must have combined with it. Accounts of these and other experiments and ideas were published in 1668 in his work Tractatus duo in the tract De respiratione. Robert Hooke, Ole Borch, Mikhail Lomonosov, and Pierre Bayen all produced oxygen in experiments in the 17th and the 18th century but none of them recognized it as a chemical element. This may have been in part due to the prevalence of the philosophy of combustion and corrosion called the phlogiston theory, which was then the favored explanation of those processes. Established in 1667 by the German alchemist J. J. Becher, one part, called phlogiston, was given off when the substance containing it was burned, while the dephlogisticated part was thought to be its true form, or calx. The fact that a substance like wood gains overall weight in burning was hidden by the buoyancy of the combustion products
22.
Solid solution
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A solid solution is a solid-state solution of one or more solutes in a solvent. The solid solution needs to be distinguished from a mechanical mixtures of powdered solids like two salts, sugar and salt, etc, the mechanical mixtures have total or partial miscibility gap in solid state. Examples of solid solutions include crystallized salts from their liquid mixture, metal alloys, in the case of metal alloys intermetallic compounds occur frequently. The solute may incorporate into the solvent crystal lattice substitutionally, by replacing a solvent particle in the lattice, or interstitially, by fitting into the space between solvent particles. Both of these types of solid solution affect the properties of the material by distorting the crystal lattice, some mixtures will readily form solid solutions over a range of concentrations, while other mixtures will not form solid solutions at all. The propensity for any two substances to form a solution is a complicated matter involving the chemical, crystallographic. 1 displays an alloy of two metals which forms a solution at all relative concentrations of the two species. Solid solutions have important commercial and industrial applications, as such mixtures often have superior properties to pure materials, many metal alloys are solid solutions. Even small amounts of solute can affect the electrical and physical properties of the solvent, the binary phase diagram in Fig.2 shows the phases of a mixture of two substances in varying concentrations, A and B. The region labeled α is a solution, with B acting as the solute in a matrix of A. On the other end of the scale, the region labeled β is also a solid solution. The large solid region in between the α and β solid solutions, labeled α + β, is not a solid solution, at other proportions, the material will enter a mushy or pasty phase until it warms up to being completely melted. The mixture at the dip point of the diagram is called a eutectic alloy, lead-tin mixtures formulated at that point are useful when soldering electronic components, particularly if done manually, since the solid phase is quickly entered as the solder cools. In contrast, when lead-tin mixtures were used to solder seams in automobile bodies a pasty state enabled a shape to be formed with a paddle or tool. When a solid solution becomes unstable — due to a temperature, for example — exsolution occurs. This is mainly caused by difference in cation size, cations which have a large difference in radii are not likely to readily substitute. Take the alkali feldspar minerals for example, whose end members are albite, NaAlSi3O8 and microcline and this leads to exsolution where they will separate into two separate phases. In the case of the feldspar minerals, thin white albite layers will alternate between typically pink microcline
23.
Forsterite
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Forsterite is the magnesium-rich end-member of the olivine solid solution series. It is isomorphous with the iron-rich end-member, fayalite, forsterite crystallizes in the orthorhombic system with cell parameters a 4.75 Å, b 10.20 Å and c 5.98 Å. Forsterite is associated with igneous and metamorphic rocks and has also found in meteorites. In 2005 it was found in cometary dust returned by the Stardust probe. In 2011 it was observed as tiny crystals in the dusty clouds of gas around a forming star, two polymorphs of forsterite are known, wadsleyite and ringwoodite. Both are mainly known from meteorites, peridot is the gemstone variety of forsterite olivine. Forsterite reacts with quartz to form the orthopyroxene mineral enstatite in the following reaction, pure forsterite is composed of magnesium, oxygen and silicon. Other minerals such as monticellite, an uncommon mineral, share the olivine structure. Monticellite is found in contact metamorphosed dolomites, forsterite-rich olivine is the most abundant mineral in the mantle above a depth of about 400 km, pyroxenes are also important minerals in this upper part of the mantle. Due to its melting point, olivine crystals are the first minerals to precipitate from a magmatic melt in a cumulate process. Forsterite-rich olivine is a common product of mantle-derived magma. Olivine in mafic and ultramafic rocks typically is rich in the forsterite end-member, forsterite also occurs in dolomitic marble which results from the metamorphism of high magnesium limestones and dolostones. Nearly pure forsterite occurs in some metamorphosed serpentinites, fayalite-rich olivine is much less common. Nearly pure fayalite is a constituent in some granite-like rocks. Forsterite is mainly composed of the anion SiO44− and the cation Mg2+ in a molar ratio 1,2, silicon is the central atom in the SiO44− anion. Each oxygen atom is bonded to the silicon by a covalent bond. The four oxygen atoms have a negative charge because of the covalent bond with silicon. Therefore, oxygen atoms need to stay far from other in order to reduce the repulsive force between them
24.
Fayalite
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Fayalite, also called iron chrysolite, is the iron-rich end-member of the olivine solid-solution series. In common with all minerals in the group, fayalite crystallizes in the orthorhombic system with cell parameters a 4.82 Å, b 10.48 Å and c Å6.09. Fayalite forms solid solution series with the magnesium olivine endmember forsterite and its main occurrence is in ultramafic volcanic and plutonic rocks and less commonly in felsic plutonic rocks and rarely in granite pegmatite. It also occurs in lithophysae in obsidian and it also occurs in medium-grade thermally metamorphosed iron-rich sediments and in impure carbonate rocks. Fayalite is stable with quartz at low pressures, whereas more magnesian olivine is not, iron stabilizes the olivine + quartz pair. The pressure and compositional dependence of the reaction can be used to calculate constraints on pressures at which assemblages of olivine + quartz formed, fayalite can also react with oxygen to produce magnetite + quartz, the three minerals together make up the FMQ oxygen buffer. The reaction is used to control the fugacity of oxygen in laboratory experiments and it can also be used to calculate the fugacity of oxygen recorded by mineral assemblages in metamorphic and igneous processes. 6–7 GPa, i. e. at substantially lower pressure than the phase transitions of forsterite, the name fayalite is derived from Faial Island in the Azores where it was first described in 1840. Forsterite, the magnesium-rich end-member of the olivine solid-solution series, mineral redox buffer Deer, W. A. Howie, R. A. and Zussman, J. An introduction to the rock-forming minerals
25.
Mole (unit)
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The mole is the unit of measurement in the International System of Units for amount of substance. This number is expressed by the Avogadro constant, which has a value of 6. 022140857×1023 mol−1, the mole is one of the base units of the SI, and has the unit symbol mol. The mole is used in chemistry as a convenient way to express amounts of reactants and products of chemical reactions. For example, the chemical equation 2 H2 + O2 →2 H2O implies that 2 moles of dihydrogen and 1 mole of dioxygen react to form 2 moles of water. The mole may also be used to express the number of atoms, ions, the concentration of a solution is commonly expressed by its molarity, defined as the number of moles of the dissolved substance per litre of solution. For example, the relative molecular mass of natural water is about 18.015, therefore. The term gram-molecule was formerly used for essentially the same concept, the term gram-atom has been used for a related but distinct concept, namely a quantity of a substance that contains Avogadros number of atoms, whether isolated or combined in molecules. Thus, for example,1 mole of MgBr2 is 1 gram-molecule of MgBr2 but 3 gram-atoms of MgBr2, in honor of the unit, some chemists celebrate October 23, which is a reference to the 1023 scale of the Avogadro constant, as Mole Day. Some also do the same for February 6 and June 2, thus, by definition, one mole of pure 12C has a mass of exactly 12 g. It also follows from the definition that X moles of any substance will contain the number of molecules as X moles of any other substance. The mass per mole of a substance is called its molar mass, the number of elementary entities in a sample of a substance is technically called its amount. Therefore, the mole is a convenient unit for that physical quantity, one can determine the chemical amount of a known substance, in moles, by dividing the samples mass by the substances molar mass. Other methods include the use of the volume or the measurement of electric charge. The mass of one mole of a substance depends not only on its molecular formula, since the definition of the gram is not mathematically tied to that of the atomic mass unit, the number NA of molecules in a mole must be determined experimentally. The value adopted by CODATA in 2010 is NA =6. 02214129×1023 ±0. 00000027×1023, in 2011 the measurement was refined to 6. 02214078×1023 ±0. 00000018×1023. The number of moles of a sample is the sample mass divided by the mass of the material. The history of the mole is intertwined with that of mass, atomic mass unit, Avogadros number. The first table of atomic mass was published by John Dalton in 1805
26.
Manganese
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Manganese is a chemical element with symbol Mn and atomic number 25. It is not found as an element in nature, it is often found in minerals in combination with iron. Manganese is a metal with important industrial metal alloy uses, particularly in stainless steels, by the mid-18th century, Swedish chemist Carl Wilhelm Scheele had used pyrolusite to produce chlorine. Scheele and others were aware that pyrolusite contained a new element, johan Gottlieb Gahn was the first to isolate an impure sample of manganese metal in 1774, which he did by reducing the dioxide with carbon. Manganese phosphating is used for rust and corrosion prevention on steel, ionized manganese is used industrially as pigments of various colors, which depend on the oxidation state of the ions. The permanganates of alkali and alkaline earth metals are powerful oxidizers, Manganese dioxide is used as the cathode material in zinc-carbon and alkaline batteries. In biology, manganese ions function as cofactors for a variety of enzymes with many functions. Manganese enzymes are essential in detoxification of superoxide free radicals in organisms that must deal with elemental oxygen. Manganese also functions in the complex of photosynthetic plants. The element is a trace mineral for all known living organisms but is a neurotoxin. In larger amounts, and apparently with far greater effectiveness through inhalation, Manganese is a silvery-gray metal that resembles iron. It is hard and very brittle, difficult to fuse, Manganese metal and its common ions are paramagnetic. Manganese tarnishes slowly in air and oxidizes like iron in water containing dissolved oxygen, naturally occurring manganese is composed of one stable isotope, 55Mn. Eighteen radioisotopes have been isolated and described, the most stable being 53Mn with a half-life of 3.7 million years, 54Mn with a half-life of 312.3 days, and 52Mn with a half-life of 5.591 days. All of the radioactive isotopes have half-lives of less than three hours, and the majority of less than one minute. Manganese also has three meta states, Manganese is part of the iron group of elements, which are thought to be synthesized in large stars shortly before the supernova explosion. 53Mn decays to 53Cr with a half-life of 3.7 million years, because of its relatively short half-life, 53Mn is relatively rare, produced by cosmic rays impact on iron. Manganese isotopic contents are combined with chromium isotopic contents and have found application in isotope geology
27.
Nickel
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Nickel is a chemical element with symbol Ni and atomic number 28. It is a silvery-white lustrous metal with a golden tinge. Nickel belongs to the metals and is hard and ductile. Meteoric nickel is found in combination with iron, a reflection of the origin of elements as major end products of supernova nucleosynthesis. An iron–nickel mixture is thought to compose Earths inner core, use of nickel has been traced as far back as 3500 BCE. Nickel was first isolated and classified as an element in 1751 by Axel Fredrik Cronstedt. The elements name comes from a mischievous sprite of German miner mythology, Nickel, an economically important source of nickel is the iron ore limonite, which often contains 1–2% nickel. Nickels other important ore minerals include garnierite, and pentlandite, major production sites include the Sudbury region in Canada, New Caledonia in the Pacific, and Norilsk in Russia. Nickel is slowly oxidized by air at room temperature and is considered corrosion-resistant, historically, it has been used for plating iron and brass, coating chemistry equipment, and manufacturing certain alloys that retain a high silvery polish, such as German silver. About 6% of world production is still used for corrosion-resistant pure-nickel plating. Nickel-plated objects sometimes provoke nickel allergy, Nickel has been widely used in coins, though its rising price has led to some replacement with cheaper metals in recent years. Nickel is one of four elements that are ferromagnetic around room temperature, alnico permanent magnets based partly on nickel are of intermediate strength between iron-based permanent magnets and rare-earth magnets. The metal is valuable in modern times chiefly in alloys, about 60% of world production is used in nickel-steels, other common alloys and some new superalloys comprise most of the remainder of world nickel use, with chemical uses for nickel compounds consuming less than 3% of production. As a compound, nickel has a number of chemical manufacturing uses. Nickel is a nutrient for some microorganisms and plants that have enzymes with nickel as an active site. Nickel is a metal with a slight golden tinge that takes a high polish. It is one of four elements that are magnetic at or near room temperature. Its Curie temperature is 355 °C, meaning that bulk nickel is non-magnetic above this temperature, the unit cell of nickel is a face-centered cube with the lattice parameter of 0.352 nm, giving an atomic radius of 0.124 nm
28.
Tephroite
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Tephroite is the manganese endmember of the olivine group of nesosilicate minerals with the formula Mn2SiO4. A solid solution exists between tephroite and its analogues, the group endmembers fayalite and forsterite. Divalent iron or magnesium may readily replace manganese in the crystal structure. It was first described for an occurrence at the Sterling Hill Mine and Franklin, New Jersey and it occurs in iron-manganese ore deposits and their related skarns. It also occurs in metamorphosed manganese-rich sediments and it occurs in association with, zincite, willemite, franklinite, rhodonite, jacobsite, diopside, gageite, bustamite, manganocalcite, glaucochroite, calcite, banalsite and alleghanyite. It can also be found in England and Sweden, tephroite has a hardness of 6 and a specific gravity of approximately 4.1, which is heavy for non-metallic minerals. Its name comes from the Greek tephros, ash gray, for its color and it can also be found olive-green, greenish-blue, pink, or brown. Other names for tephroite include mangan olivine and mangan peridot
29.
Monticellite
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Monticellite and kirschsteinite are gray silicate minerals of the olivine group with compositions CaMgSiO4 and CaFeSiO4, respectively. Most monticellites have the pure magnesium end-member composition but rare ferroan monticellites, pure kirschsteinite is only found in synthetic systems. Monticellite is named after Teodoro Monticelli Italian mineralogist, like other members of the group monticellite and kirschsteinite have orthorhombic unit cells shown in Figure 1. Iron and magnesium ions are located on the M1 inversion sites, deer, W. A. Howie, R. A. and Zussman, J. An introduction to the rock-forming minerals, harlow, Longman ISBN 0-582-30094-0 Mindat. org Webmineral. com Handbook of Mineralogy
30.
Calcium
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Calcium is a chemical element with symbol Ca and atomic number 20. Calcium is a soft grayish-yellow alkaline earth metal, fifth-most-abundant element by mass in the Earths crust, the ion Ca2+ is also the fifth-most-abundant dissolved ion in seawater by both molarity and mass, after sodium, chloride, magnesium, and sulfate. Free calcium metal is too reactive to occur in nature, Calcium is produced in supernova nucleosynthesis. Calcium is a trace element in living organisms. It is the most abundant metal by mass in animals, and it is an important constituent of bone, teeth. In cell biology, the movement of the calcium ion into, Calcium carbonate and calcium citrate are often taken as dietary supplements. Calcium is on the World Health Organizations List of Essential Medicines, Calcium has a wide variety of applications, almost all of which are associated with calcium compounds and salts. Calcium metal is used as a deoxidizer, desulfurizer, and decarbonizer for production of ferrous and nonferrous alloys. In steelmaking and production of iron, Ca reacts with oxygen, Calcium carbonate is used in manufacturing cement and mortar, lime, limestone and aids in production in the glass industry. It also has chemical and optical uses as mineral specimens in toothpastes, Calcium hydroxide solution is used to detect the presence of carbon dioxide in a gas sample bubbled through a solution. The solution turns cloudy where CO2 is present, Calcium arsenate is used in insecticides. Calcium carbide is used to make acetylene gas and various plastics, Calcium chloride is used in ice removal and dust control on dirt roads, as a conditioner for concrete, as an additive in canned tomatoes, and to provide body for automobile tires. Calcium citrate is used as a food preservative, Calcium cyclamate is used as a sweetening agent in several countries. In the United States, it has been outlawed as a suspected carcinogen, Calcium gluconate is used as a food additive and in vitamin pills. Calcium hypochlorite is used as a swimming pool disinfectant, as an agent, as an ingredient in deodorant. Calcium permanganate is used in rocket propellant, textile production, as a water sterilizing agent. Calcium phosphate is used as a supplement for animal feed, fertilizer, in production for dough and yeast products, in the manufacture of glass. Calcium phosphide is used in fireworks, rodenticide, torpedoes, Calcium sulfate is used as common blackboard chalk, as well as, in its hemihydrate form, Plaster of Paris
31.
Bravais lattice
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This discrete set of vectors must be closed under vector addition and subtraction. For any choice of position vector R, the lattice looks exactly the same, when the discrete points are atoms, ions, or polymer strings of solid matter, the Bravais lattice concept is used to formally define a crystalline arrangement and its frontiers. A crystal is made up of an arrangement of one or more atoms repeated at each lattice point. Consequently, the crystal looks the same when viewed from any equivalent lattice point, two Bravais lattices are often considered equivalent if they have isomorphic symmetry groups. In this sense, there are 14 possible Bravais lattices in three-dimensional space, the 14 possible symmetry groups of Bravais lattices are 14 of the 230 space groups. In two-dimensional space, there are 5 Bravais lattices, grouped into four crystal families, the unit cells are specified according to the relative lengths of the cell edges and the angle between them. The area of the cell can be calculated by evaluating the norm || a × b ||. The properties of the families are given below, In three-dimensional space. These are obtained by combining one of the six families with one of the centering types. For example, the monoclinic I lattice can be described by a monoclinic C lattice by different choice of crystal axes, similarly, all A- or B-centred lattices can be described either by a C- or P-centering. This reduces the number of combinations to 14 conventional Bravais lattices, the unit cells are specified according to the relative lengths of the cell edges and the angles between them. The volume of the cell can be calculated by evaluating the triple product a ·, where a, b. The properties of the families are given below, In four dimensions. Of these,23 are primitive and 41 are centered, ten Bravais lattices split into enantiomorphic pairs. Bravais, A. Mémoire sur les systèmes formés par les points distribués régulièrement sur un plan ou dans lespace, hahn, Theo, ed. International Tables for Crystallography, Volume A, Space Group Symmetry. Catalogue of Lattices Smith, Walter Fox
32.
Spinel
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Spinel is the magnesium aluminium member of the larger spinel group of minerals. It has the formula MgAl2O4 in the crystal system. Its name comes from Latin spina, balas ruby is an old name for a rose-tinted variety of spinel. Spinel crystallizes in the system, common crystal forms are octahedra. It has an imperfect cleavage and a conchoidal fracture. Its hardness is 8, its gravity is 3. 5–4.1. It may be colorless, but is usually shades of red, blue, green, yellow, brown, black. There is a natural white spinel, now lost, that surfaced briefly in what is now Sri Lanka. The Samarian Spinel is the largest known spinel in the world, the transparent red spinels were called spinel-rubies or balas rubies. In the past, before the arrival of modern science, spinels, after the 18th century the word ruby was only used for the red gem variety of the mineral corundum and the word spinel came to be used. Balas is derived from Balascia, the ancient name for Badakhshan, mines in the Gorno Badakhshan region of Tajikistan was for centuries the main source for red and pink spinels. Spinel has long been found in the gravel of Sri Lanka and in limestones of the Badakshan Province in modern-day Afghanistan and Tajikistan. Recently gem quality spinels also found in the marbles of Luc Yen, Mahenge and Matombo, Tsavo and in the gravels of Tunduru and this is why spinel and ruby are often found together. Spinel, 2O4, is common in peridotite in the uppermost Earths mantle, Spinel, Al2O4, is a common mineral in the Ca-Al-rich inclusions in some chondritic meteorites. Synthetic spinel, accidentally produced in the middle of the 18th century, has described more recently in scientific publications in 2000 and 2004. By 2015, transparent spinel was being made in sheets and other shapes through sintering, synthetic spinel which looks like glass but has notably higher strength against pressure, can also have applications in military and commercial use. Spinel group Ceylonite The Samarian Spinel, the largest known spinel in the world, part of the Iranian Crown Jewels Black Princes Ruby Deer, Howie, an Introduction to the Rock-Forming Minerals, Longman, pp. 424–433, ISBN 0-582-44210-9. Gemstones of the World 3rd edition, Sterling, pp. 116–117, Spinel structure at the University of Wisconsin - Green Bay Spinel structure at the Institut for materials science of the University of Kiel Value of Spinel
33.
Gemstone
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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
34.
Peridot
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Peridot is gem-quality olivine, which is a silicate mineral with the formula of 2SiO4. As peridot is the variety of olivine, the formula approaches Mg2SiO4. The origin of the name peridot is uncertain, the Oxford English Dictionary suggests an alteration of Anglo–Norman pedoretés, a kind of opal, rather than the Arabic word faridat, meaning gem. The Middle English Dictionarys entry on peridot includes several variations, peridod, peritot, the earliest use in England is in the register of the St Albans Abbey, in Latin, and its translation in 1705 is possibly the first use of peridot in English. It records that on his death in 1245, Bishop John bequeathed various items including peridot to the Abbey, Peridot is one of the few gemstones that occur in only one color, an olive-green. In rare cases, peridot may occur in a medium-dark toned, peridots can also be found in meteorites. Olivine in general is an abundant mineral, but gem quality peridot is rather rare. This is due to the chemical instability on the Earths surface. Olivine is usually found as small grains, and tends to exist in a heavily weathered state, large crystals of forsterite, the variety most often used to cut peridot gems, are rare, as a result olivine is considered to be precious. Peridot crystals have been collected from some pallasite meteorites, Peridot is sometimes mistaken for emeralds and other green gems. Notable gemologist George Frederick Kunz discussed the confusion between emeralds and peridots in many church treasures, notably the Three Magi treasure in the Dom of Cologne, the largest cut peridot olivine is a 310 carat specimen in the Smithsonian Museum in Washington, D. C. Peridot olivine is the birthstone for the month of August, USGS peridot data Emporia Edu Florida State University – Peridot
35.
Scots pine
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In the north of its range, it occurs from sea level to 1,000 m, while in the south of its range it is a high altitude mountain tree, growing at 1, 200–2,600 m altitude. It is readily identified by its combination of short, blue-green leaves. The species is found on poorer, sandy soils, rocky outcrops. On fertile sites, Scots pine is out-competed by other, usually spruce or broad-leaved tree species and it is the national tree of Scotland. The bark is thick, scaly dark grey-brown on the lower trunk, the habit of the mature tree is distinctive due to its long, bare and straight trunk topped by a rounded or flat-topped mass of foliage. The lifespan is normally 150–300 years, with the oldest recorded specimens in Lapland, the shoots are light brown, with a spirally arranged scale-like pattern. On vigorous young trees the leaves can be twice as long, leaf persistence varies from two to four years in warmer climates, and up to nine years in subarctic regions. Seedlings up to one year old bear juvenile leaves, these are single, 2–3 cm long, flattened, the cone scales have a flat to pyramidal apophysis, with a small prickle on the umbo. The seeds are blackish, 3–5 mm in length with a pale brown 12–20 mm wing and are released when the open in spring 22–24 months after pollination. The pollen cones are yellow, occasionally pink, 8–12 mm long, over 100 Pinus sylvestris varieties have been described in the botanical literature, but only three or four are now accepted. They differ only minimally in morphology, but with more pronounced differences in genetic analysis, populations in westernmost Scotland are genetically distinct from those in the rest of Scotland and northern Europe, but not sufficiently to have been distinguished as a separate botanical variety. Trees in the far north of the range were formerly treated as var. lapponica. The bulk of the range, from Scotland and Spain to central Siberia, the Balkans, northern Turkey, Crimea, and the Caucasus. Foliage more consistently glaucous all year, not becoming duller in winter, mongolia and adjoining parts of southern Siberia and northwestern China. Foliage duller green, shoots grey-green, leaves occasionally up to 12 cm long, the Sierra Nevada in southern Spain and possibly other Spanish populations Kalenicz. Cones often with scales, but doubtfully distinguishable on morphology. From border regions between Russia and Ukraine, in central and southern Europe, it occurs with numerous additional species, including European black pine, mountain pine, Macedonian pine, and Swiss pine. In the eastern part of its range, it occurs with Siberian pine, the tree spread across the British Isles after the Last Glacial Maximum
36.
Lava
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Lava is the molten rock expelled by a volcano during an eruption. The resulting rock after solidification and cooling is called lava. The molten rock is formed in the interior of planets, including Earth. The source of the heat melts the rock within the earth is geothermal energy. When first erupted from a vent, lava is a liquid usually at temperatures from 700 to 1,200 °C. A lava flow is an outpouring of lava, which is created during a non-explosive effusive eruption. When it has stopped moving, lava solidifies to form igneous rock, the term lava flow is commonly shortened to lava. Although lava can be up to 100,000 times more viscous than water, lava can flow great distances before cooling and solidifying because of its thixotropic, explosive eruptions produce a mixture of volcanic ash and other fragments called tephra, rather than lava flows. The word lava comes from Italian, and is derived from the Latin word labes which means a fall or slide. The first use in connection with extruded magma was apparently in an account written by Francesco Serao on the eruption of Vesuvius between May 14 and June 4,1737. Serao described a flow of lava as an analogy to the flow of water. The composition of almost all lava of the Earths crust is dominated by silicate minerals, mostly feldspars, olivine, pyroxenes, amphiboles, micas, igneous rocks, which form lava flows when erupted, can be classified into three chemical types, felsic, intermediate, and mafic. These classes are primarily chemical, however, the chemistry of lava also tends to correlate with the temperature, its viscosity. Felsic or silicic lavas such as rhyolite and dacite typically form lava spines, most silicic lava flows are extremely viscous, and typically fragment as they extrude, producing blocky autobreccias. Felsic magmas can erupt at temperatures as low as 650 to 750 °C, unusually hot rhyolite lavas, however, may flow for distances of many tens of kilometres, such as in the Snake River Plain of the northwestern United States. Intermediate or andesitic lavas are lower in aluminium and silica, and usually somewhat richer in magnesium, intermediate lavas form andesite domes and block lavas, and may occur on steep composite volcanoes, such as in the Andes. Poorer in aluminium and silica than felsic lavas, and also commonly hotter, greater temperatures tend to destroy polymerized bonds within the magma, promoting more fluid behaviour and also a greater tendency to form phenocrysts. Higher iron and magnesium tends to manifest as a darker groundmass, mafic or basaltic lavas are typified by their high ferromagnesian content, and generally erupt at temperatures in excess of 950 °C
37.
Papakolea Beach
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Papakōlea Beach is a green sand beach located near South Point, in the Kaʻū district of the island of Hawaiʻi. One of only four green sand beaches in the world, the others being Talofofo Beach, Guam, Punta Cormorant on Floreana Island in the Galapagos Islands and it gets its distinctive coloring from olivine sand eroded out of the enclosing collapsed cinder cone. Papakōlea Beach is located in a bay half circled by Puʻu Mahana, since its last eruption, the cinder cone has partially collapsed and been partially eroded by the ocean. The beach is named after the cinder cone, and sometimes after the area of land called Papakōlea, which comes from papa kōlea. Papakōlea is the area near the crater where Pacific golden plovers are sometimes seen in winter, the cinder cone is rich in olivine, a silicate mineral containing iron and magnesium, also known as peridot when of gem quality. Olivine is a common component of Hawaiian lavas and one of the first crystals to form as magma cools. Olivine is locally known as Hawaiian Diamond and is found in Oʻahus famous Diamond Head landmark. The source of the coloration of the beach sands is due to the olivine crystals which are winnowed from the eroding headland by the action of the sea. The beach is located at coordinates 18. 936379°N155. 646315°W /18.936379, -155.646315 and it is surrounded by pasturelands and is only accessible by foot. The paths are rugged and the owner, the Department of Hawaiian Home Lands, has since restricted vehicular traffic in the area. To actually reach the beach, a climb down the cinder cone is required
38.
Hawaii
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Hawaii is the 50th and most recent state to have joined the United States of America, having received statehood on August 21,1959. Hawaii is the only U. S. state located in Oceania and it is the northernmost island group in Polynesia, occupying most of an archipelago in the central Pacific Ocean. Hawaii is the only U. S. state not located in the Americas, the state encompasses nearly the entire volcanic Hawaiian archipelago, which comprises hundreds of islands spread over 1,500 miles. At the southeastern end of the archipelago, the eight main islands are—in order from northwest to southeast, Niʻihau, Kauaʻi, Oʻahu, Molokaʻi, Lānaʻi, Kahoʻolawe, Maui, and the Island of Hawaiʻi. The last is the largest island in the group, it is called the Big Island or Hawaiʻi Island to avoid confusion with the state or archipelago. The archipelago is physiographically and ethnologically part of the Polynesian subregion of Oceania, Hawaii has over a million permanent residents, along with many visitors and U. S. military personnel. Its capital is Honolulu on the island of Oʻahu, Hawaii is the 8th-smallest and the 11th-least populous, but the 13th-most densely populated of the fifty U. S. states. It is the state with an Asian plurality. The states coastline is about 750 miles long, the fourth longest in the U. S. after the coastlines of Alaska, Florida, the state of Hawaii derives its name from the name of its largest island, Hawaiʻi. A common Hawaiian explanation of the name of Hawaiʻi is that was named for Hawaiʻiloa and he is said to have discovered the islands when they were first settled. The Hawaiian language word Hawaiʻi is very similar to Proto-Polynesian *Sawaiki, cognates of Hawaiʻi are found in other Polynesian languages, including Māori, Rarotongan and Samoan. According to linguists Pukui and Elbert, lsewhere in Polynesia, Hawaiʻi or a cognate is the name of the underworld or of the home, but in Hawaii. A somewhat divisive political issue arose in 1978 when the Constitution of the State of Hawaii added Hawaiian as an official state language. The title of the constitution is The Constitution of the State of Hawaii. Article XV, Section 1 of the Constitution uses The State of Hawaii, diacritics were not used because the document, drafted in 1949, predates the use of the okina and the kahakō in modern Hawaiian orthography. The exact spelling of the name in the Hawaiian language is Hawaiʻi. In the Hawaii Admission Act that granted Hawaiian statehood, the government recognized Hawaii as the official state name. Official government publications, department and office titles, and the Seal of Hawaii use the spelling with no symbols for glottal stops or vowel length
39.
Basalt
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Basalt is a common extrusive igneous rock formed from the rapid cooling of basaltic lava exposed at or very near the surface of a planet or moon. Flood basalt describes the formation in a series of basalt flows. By definition, basalt is an igneous rock with generally 45-55% silica and less than 10% feldspathoid by volume. Basalt commonly features a very fine-grained or glassy matrix interspersed with visible mineral grains, the average density is 3.0 gm/cm3. Basalt is defined by its content and texture, and physical descriptions without mineralogical context may be unreliable in some circumstances. Basalt is usually grey to black in colour, but rapidly weathers to brown or rust-red due to oxidation of its mafic minerals into hematite, although usually characterized as dark, basaltic rocks exhibit a wide range of shading due to regional geochemical processes. Due to weathering or high concentrations of plagioclase, some basalts can be quite light-coloured and these phenocrysts usually are of olivine or a calcium-rich plagioclase, which have the highest melting temperatures of the typical minerals that can crystallize from the melt. Basalt with a texture is called vesicular basalt, when the bulk of the rock is mostly solid. Gabbro is often marketed commercially as black granite and these ultramafic volcanic rocks, with silica contents below 45% are usually classified as komatiites. Agricola applied basalt to the black rock of the Schloßberg at Stolpen. Tholeiitic basalt is relatively rich in silica and poor in sodium, included in this category are most basalts of the ocean floor, most large oceanic islands, and continental flood basalts such as the Columbia River Plateau. Basalt rocks are in some cases classified after their content in High-Ti and Low-Ti varieties. High-Ti and Low-Ti basalts have been distinguished in the Paraná and Etendeka traps and it has greater than 17% alumina and is intermediate in composition between tholeiite and alkali basalt, the relatively alumina-rich composition is based on rocks without phenocrysts of plagioclase. Alkali basalt is relatively poor in silica and rich in sodium and it is silica-undersaturated and may contain feldspathoids, alkali feldspar and phlogopite. Boninite is a form of basalt that is erupted generally in back-arc basins. Ocean island basalt Lunar basalt On Earth, most basalt magmas have formed by melting of the mantle. Basalt commonly erupts on Io, the third largest moon of Jupiter, and has formed on the Moon, Mars, Venus. The crustal portions of oceanic tectonic plates are composed predominantly of basalt, produced from upwelling mantle below, the mineralogy of basalt is characterized by a preponderance of calcic plagioclase feldspar and pyroxene
40.
Apollo 15
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Apollo 15 was the ninth manned mission in the United States Apollo program, the fourth to land on the Moon, and the eighth successful manned mission. It was the first of what were termed J missions, long stays on the Moon and it was also the first mission on which the Lunar Roving Vehicle was used. The mission began on July 26,1971, and ended on August 7, at the time, NASA called it the most successful manned flight ever achieved. Commander David Scott and Lunar Module Pilot James Irwin spent three days on the Moon, including 18½ hours outside the spacecraft on lunar extra-vehicular activity, the mission landed near Hadley rille, in an area of the Mare Imbrium called Palus Putredinus. The crew explored the area using the first lunar rover, which allowed them to travel farther from the Lunar Module than had been possible on missions without the rover. They collected 77 kilograms of lunar surface material, Scott had attended the University of Michigan, but left before graduating to accept an appointment to the United States Military Academy. The crewmen did their work at either the United States Military Academy or the United States Naval Academy. C. Gordon Fullerton Joseph P. Allen Robert A. Parker Karl G.5 km Apogee,171.3 km Inclination,29. 679° Period,87. There had been a rivalry between that prime and backup crew on that mission, with the prime being all United States Navy. Originally Apollo 15 would have been an H mission, like Apollos 12,13 and 14, but on September 2,1970, NASA announced it was canceling what were to be the current incarnations of the Apollo 15 and Apollo 19 missions. To maximize the return from the missions, Apollo 15 would now fly as a J mission and have the honor of carrying the first lunar rover. One of the changes in the training for Apollo 15 was the geology training. Although on previous flights the crews had trained in field geology. Scott and Irwin would train with Leon Silver, a Caltech geologist who on Earth was interested in the Precambrian, Silver had been suggested by Harrison Schmitt as an alternative to the classroom lecturers that NASA had previously used. Among other things, Silver had made important refinements to the methods for dating rocks using the decay of uranium into lead in the late 1950s, crews began to wear mock-ups of the backpacks they would carry, and communicate using walkie-talkies to a CAPCOM in a tent. The CAPCOM was accompanied by a group of geologists unfamiliar with the area who would rely on the descriptions to interpret the findings. The decision to land at Hadley came in September 1970, the Site Selection Committees had narrowed the field down to two sites — Hadley Rille or the crater Marius, near which were a group of low, possibly volcanic, domes. Although not ultimately his decision, the commander of a mission always held great sway, to David Scott the choice was clear, with Hadley, being exploration at its finest
41.
French language
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French is a Romance language of the Indo-European family. It descended from the Vulgar Latin of the Roman Empire, as did all Romance languages, French has evolved from Gallo-Romance, the spoken Latin in Gaul, and more specifically in Northern Gaul. Its closest relatives are the other langues doïl—languages historically spoken in northern France and in southern Belgium, French was also influenced by native Celtic languages of Northern Roman Gaul like Gallia Belgica and by the Frankish language of the post-Roman Frankish invaders. Today, owing to Frances past overseas expansion, there are numerous French-based creole languages, a French-speaking person or nation may be referred to as Francophone in both English and French. French is a language in 29 countries, most of which are members of la francophonie. As of 2015, 40% of the population is in Europe, 35% in sub-Saharan Africa, 15% in North Africa and the Middle East, 8% in the Americas. French is the fourth-most widely spoken mother tongue in the European Union, 1/5 of Europeans who do not have French as a mother tongue speak French as a second language. As a result of French and Belgian colonialism from the 17th and 18th century onward, French was introduced to new territories in the Americas, Africa, most second-language speakers reside in Francophone Africa, in particular Gabon, Algeria, Mauritius, Senegal and Ivory Coast. In 2015, French was estimated to have 77 to 110 million native speakers, approximately 274 million people are able to speak the language. The Organisation internationale de la Francophonie estimates 700 million by 2050, in 2011, Bloomberg Businessweek ranked French the third most useful language for business, after English and Standard Mandarin Chinese. Under the Constitution of France, French has been the language of the Republic since 1992. France mandates the use of French in official government publications, public education except in specific cases, French is one of the four official languages of Switzerland and is spoken in the western part of Switzerland called Romandie, of which Geneva is the largest city. French is the language of about 23% of the Swiss population. French is also a language of Luxembourg, Monaco, and Aosta Valley, while French dialects remain spoken by minorities on the Channel Islands. A plurality of the worlds French-speaking population lives in Africa and this number does not include the people living in non-Francophone African countries who have learned French as a foreign language. Due to the rise of French in Africa, the total French-speaking population worldwide is expected to reach 700 million people in 2050, French is the fastest growing language on the continent. French is mostly a language in Africa, but it has become a first language in some urban areas, such as the region of Abidjan, Ivory Coast and in Libreville. There is not a single African French, but multiple forms that diverged through contact with various indigenous African languages, sub-Saharan Africa is the region where the French language is most likely to expand, because of the expansion of education and rapid population growth
42.
Greek language
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Greek is an independent branch of the Indo-European family of languages, native to Greece and other parts of the Eastern Mediterranean. It has the longest documented history of any living language, spanning 34 centuries of written records and its writing system has been the Greek alphabet for the major part of its history, other systems, such as Linear B and the Cypriot syllabary, were used previously. The alphabet arose from the Phoenician script and was in turn the basis of the Latin, Cyrillic, Armenian, Coptic, Gothic and many other writing systems. Together with the Latin texts and traditions of the Roman world, during antiquity, Greek was a widely spoken lingua franca in the Mediterranean world and many places beyond. It would eventually become the official parlance of the Byzantine Empire, the language is spoken by at least 13.2 million people today in Greece, Cyprus, Italy, Albania, Turkey, and the Greek diaspora. Greek roots are used to coin new words for other languages, Greek. Greek has been spoken in the Balkan peninsula since around the 3rd millennium BC, the earliest written evidence is a Linear B clay tablet found in Messenia that dates to between 1450 and 1350 BC, making Greek the worlds oldest recorded living language. Among the Indo-European languages, its date of earliest written attestation is matched only by the now extinct Anatolian languages, the Greek language is conventionally divided into the following periods, Proto-Greek, the unrecorded but assumed last ancestor of all known varieties of Greek. The unity of Proto-Greek would have ended as Hellenic migrants entered the Greek peninsula sometime in the Neolithic era or the Bronze Age, Mycenaean Greek, the language of the Mycenaean civilisation. It is recorded in the Linear B script on tablets dating from the 15th century BC onwards, Ancient Greek, in its various dialects, the language of the Archaic and Classical periods of the ancient Greek civilisation. It was widely known throughout the Roman Empire, after the Roman conquest of Greece, an unofficial bilingualism of Greek and Latin was established in the city of Rome and Koine Greek became a first or second language in the Roman Empire. The origin of Christianity can also be traced through Koine Greek, Medieval Greek, also known as Byzantine Greek, the continuation of Koine Greek in Byzantine Greece, up to the demise of the Byzantine Empire in the 15th century. Much of the written Greek that was used as the language of the Byzantine Empire was an eclectic middle-ground variety based on the tradition of written Koine. Modern Greek, Stemming from Medieval Greek, Modern Greek usages can be traced in the Byzantine period and it is the language used by the modern Greeks, and, apart from Standard Modern Greek, there are several dialects of it. In the modern era, the Greek language entered a state of diglossia, the historical unity and continuing identity between the various stages of the Greek language is often emphasised. Greek speakers today still tend to regard literary works of ancient Greek as part of their own rather than a foreign language and it is also often stated that the historical changes have been relatively slight compared with some other languages. According to one estimation, Homeric Greek is probably closer to demotic than 12-century Middle English is to modern spoken English, Greek is spoken by about 13 million people, mainly in Greece, Albania and Cyprus, but also worldwide by the large Greek diaspora. Greek is the language of Greece, where it is spoken by almost the entire population
43.
Gold
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Gold is a chemical element with symbol Au and atomic number 79. In its purest form, it is a bright, slightly yellow, dense, soft, malleable. Chemically, gold is a metal and a group 11 element. It is one of the least reactive chemical elements and is solid under standard conditions, Gold often occurs in free elemental form, as nuggets or grains, in rocks, in veins, and in alluvial deposits. It occurs in a solid solution series with the element silver and also naturally alloyed with copper. Less commonly, it occurs in minerals as gold compounds, often with tellurium, golds atomic number of 79 makes it one of the higher numbered, naturally occurring elements. It is thought to have produced in supernova nucleosynthesis, from the collision of neutron stars. Because the Earth was molten when it was formed, almost all of the present in the early Earth probably sank into the planetary core. Gold is resistant to most acids, though it does dissolve in aqua regia, a mixture of acid and hydrochloric acid. Gold also dissolves in solutions of cyanide, which are used in mining and electroplating. Gold dissolves in mercury, forming amalgam alloys, but this is not a chemical reaction, as a precious metal, gold has been used for coinage, jewelry, and other arts throughout recorded history. A total of 186,700 tonnes of gold is in existence above ground, the world consumption of new gold produced is about 50% in jewelry, 40% in investments, and 10% in industry. Gold is also used in infrared shielding, colored-glass production, gold leafing, certain gold salts are still used as anti-inflammatories in medicine. As of 2014, the worlds largest gold producer by far was China with 450 tonnes, Gold is cognate with similar words in many Germanic languages, deriving via Proto-Germanic *gulþą from Proto-Indo-European *ǵʰelh₃-. The symbol Au is from the Latin, aurum, the Latin word for gold, the Proto-Indo-European ancestor of aurum was *h₂é-h₂us-o-, meaning glow. This word is derived from the root as *h₂éu̯sōs, the ancestor of the Latin word Aurora. This etymological relationship is presumably behind the frequent claim in scientific publications that aurum meant shining dawn, Gold is the most malleable of all metals, a single gram can be beaten into a sheet of 1 square meter, and an avoirdupois ounce into 300 square feet. Gold leaf can be thin enough to become semi-transparent
44.
Mantle (geology)
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The mantle is a layer inside a terrestrial planet and some other rocky planetary bodies. For a mantle to form, the body must be large enough to have undergone the process of planetary differentiation by density. The mantle surrounds the planetary core, the mantle is surrounded by the crust. The terrestrial planets, the Moon, two of Jupiters moons and the asteroid Vesta each have a made of silicate rock. Interpretation of spacecraft data suggests that at least two moons of Jupiter, as well as Titan and Triton each have a mantle made of ice or other solid volatile substances. The interior of Earth, similar to the terrestrial planets, is divided into layers of different composition. The mantle is a layer between the crust and the outer core, Earths mantle is a silicate rocky shell with an average thickness of 2,886 kilometres. The mantle makes up about 84% of Earths volume and it is predominantly solid but in geological time it behaves as a very viscous fluid. The mantle encloses the hot core rich in iron and nickel, past episodes of melting and volcanism at the shallower levels of the mantle have produced a thin crust of crystallized melt products near the surface. A thin crust, the part of the lithosphere, surrounds the mantle and is about 5 to 75 km thick. In some places under the ocean the mantle is exposed on the surface of Earth. The mantle is divided into sections which are based upon results from seismology and these layers are the following, the upper mantle, the transition zone, the lower mantle, and anomalous core–mantle boundary with a variable thickness. The uppermost mantle plus overlying crust are relatively rigid and form the lithosphere, below the lithosphere the upper mantle becomes notably more plastic. In some regions below the lithosphere, the shear velocity is reduced. Inge Lehmann discovered a seismic discontinuity at about 220 km depth, although this discontinuity has been found in other studies, the transition zone is an area of great complexity, it physically separates the upper and lower mantle. Very little is known about the lower mantle apart from that it appears to be relatively seismically homogeneous, the D layer at the core–mantle boundary separates the mantle from the core. A principal source of the heat that drives plate tectonics is the decay of uranium, thorium. The mantle differs substantially from the crust in its properties as the direct consequence of the difference in composition
45.
Zabargad Island
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Zabargad Island is the largest of a group of islands in Foul Bay, Egypt. It covers an area of 4.50 square kilometres and it is not a quaternary volcanic island, but rather is believed to be an upthrusted part of upper mantle material. The nearest island is known as Rocky Island, the island is slightly north of the Tropic of Cancer, and its highest point is 235 metres. Pliny, HN37,108 refers to a large topaz that was back to Egypt as a gift for Ptolemy Is queen Berenice I. The island is considered unique as it is uplifted mantle. Rocks on the island are mainly lower crustal metamorphic rocks, the island became present above sea level after African and Asiatic continental plates converged to cause rocks in the lower crust to be uplifted. The island comprises three massives of peridotite, which are rich in the gemstone peridot. This gem makes the island notable as it is believed to be the first discovered source of peridot, layers of spinel-lherzolites with anhydrous Al-diopside pyroxenites and hydrous Cr-diopside pyroxenites can be found too on the island. The presence of all of these minerals has led to mining on the island dates back as early as ancient times. Pliny, XXXV, chap.22 says that, according to Juba, the island Topazus in the Red Sea, also had mines producing sandarach and ochre, the island is part of the Elba National Park meaning the island is conserved. However, the island was closed to the public for one due to damage to corals. The island serves as a ground for at least 9 known species of birds. The most recent discovery was that of 150 pairs of sooty falcon in October,1994, there is very little vegetation on the island due to the lack of soil. The corals surround the island and act as a barrier for the fish, however, the corals recently became damaged due to increased tourist activity and the expansion of the diving industry on the island. The coral is located approximately 25 metres below the surface, fish that can be found within the nearby waters and corals are, Rays Moray eels Octopus Crocodilefish Cuttlefish The island is near coral reefs, which are a popular diving attraction for tourists. The diving industry on the island has increased as well as the industry on the island in general resulting in construction of hotels. The beaches are often quiet and are relatively unspoilt by development, however, most tourists go to this island as a stop-off before going to Rocky Island in the south. St. Johns Island peridot information and history at Mindat. org Bird Life Information Diving Egypts Marine Park Islands Diving Information red sea dive safaris covering all the red sea
46.
Red Sea
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The Red Sea is a seawater inlet of the Indian Ocean, lying between Africa and Asia. The connection to the ocean is in the south through the Bab el Mandeb strait, to the north lie the Sinai Peninsula, the Gulf of Aqaba, and the Gulf of Suez. The Red Sea is a Global 200 ecoregion, the sea is underlain by the Red Sea Rift which is part of the Great Rift Valley. The Red Sea has an area of roughly 438,000 km2, is about 2250 km long and. It has a depth of 2211 m in the central median trench. However, there are also extensive shallow shelves, noted for their marine life, the sea is the habitat of over 1,000 invertebrate species, and 200 soft and hard corals. It is the worlds northernmost tropical sea, the International Hydrographic Organization defines the limits of the Red Sea as follows, On the North. The Southern limits of the Gulfs of Suez and Aqaba, a line joining Husn Murad and Ras Siyyan. Red Sea is a translation of the Greek Erythra Thalassa, Latin Mare Rubrum, Arabic, البحر الأحمر. Al-Baḥr Al-Aḥmar, Somali Badda Cas and Tigrinya Qeyyiḥ bāḥrī, the name of the sea may signify the seasonal blooms of the red-coloured Trichodesmium erythraeum near the waters surface. A theory favored by modern scholars is that the name red is referring to the direction south. The basis of this theory is that some Asiatic languages used color words to refer to the cardinal directions, herodotus on one occasion uses Red Sea and Southern Sea interchangeably. Historically, it was known to western geographers as Mare Mecca. Some ancient geographers called the Red Sea the Arabian Gulf or Gulf of Arabia. C, in that version, the Yam Suph is translated as Erythra Thalassa. The Red Sea is one of four seas named in English after common color terms — the others being the Black Sea, the White Sea and the Yellow Sea. The direct rendition of the Greek Erythra thalassa in Latin as Mare Erythraeum refers to the part of the Indian Ocean. The earliest known exploration of the Red Sea was conducted by ancient Egyptians, one such expedition took place around 2500 BC, and another around 1500 BC. Both involved long voyages down the Red Sea, historically, scholars argued whether these trips were possible
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Mafic
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Mafic is an adjective describing a silicate mineral or igneous rock that is rich in magnesium and iron, and is thus a portmanteau of magnesium and ferric. Most mafic minerals are dark in color, and common rock-forming mafic minerals include olivine, pyroxene, amphibole, common mafic rocks include basalt, dolerite and gabbro. Mafic rocks often also contain calcium-rich varieties of plagioclase feldspar, chemically, mafic rocks are on the other side of the rock spectrum from the felsic rocks. The term roughly corresponds to the basic rock class. Mafic lava, before cooling, has a low viscosity, in comparison to felsic lava, water and other volatiles can more easily and gradually escape from mafic lava. As a result, eruptions of volcanoes made of mafic lavas are less violent than felsic-lava eruptions. Most mafic-lava volcanoes are shield volcanoes, like those in Hawaii, QAPF diagram List of minerals List of rock types
. Bibcode:2012Natur.490...74D. doi:10.1038/nature11469. PMID 23038467.[permanent dead link]
