Crystal twinning in the context of "Cerussite"

Play Trivia Questions online!

or

Skip to study material about Crystal twinning in the context of "Cerussite"

Ad spacer

⭐ Core Definition: Crystal twinning

Crystal twinning occurs when two or more adjacent crystals of the same mineral are oriented so that they share some of the same crystal lattice points in a symmetrical manner. The result is an intergrowth of two separate crystals that are tightly bonded to each other. The surface along which the lattice points are shared in twinned crystals is called a composition surface or twin plane.

In crystallography twinned crystals are described by a number of twin laws, which are specific to the crystal structure. The type of twinning can be a diagnostic tool in mineral identification. There are three main types of twinning. The first is growth twinning which can occur both in very large and very small particles. The second is transformation twinning, where there is a change in the crystal structure. The third is deformation twinning, in which twinning develops in a crystal in response to a shear stress, and is an important mechanism for permanent shape changes in a crystal.

↓ Menu

>>>PUT SHARE BUTTONS HERE<<<
In this Dossier

Crystal twinning in the context of Tin

Tin is a chemical element; it has the symbol Sn (from Latin stannum) and atomic number 50. A metallic-gray metal, tin is soft enough to be cut with little force, and a bar of tin can be bent by hand with little effort. When bent, a bar of tin makes a sound, the so-called "tin cry", as a result of twinning in tin crystals.

Tin is a post-transition metal in group 14 of the periodic table of elements. It is obtained chiefly from the mineral cassiterite, which contains stannic oxide, SnO
2
. Tin shows a chemical similarity to both of its neighbors in group 14, germanium and lead, and has two main oxidation states, +2 and the slightly more stable +4. Tin is the 49th most abundant element on Earth, making up 0.00022% of its crust, and with 10 stable isotopes, it has the largest number of stable isotopes in the periodic table, due to its magic number of protons.

↑ Return to Menu

Crystal twinning in the context of Plagioclase

Plagioclase (/ˈplæ(i)əˌkls, ˈpl-, -ˌklz/ PLAJ-(ee)-ə-klayss, PLAYJ-, -⁠klayz) is a series of tectosilicate (framework silicate) minerals within the feldspar group. Rather than referring to a particular mineral with a specific chemical composition, plagioclase is a continuous solid solution series, more properly known as the plagioclase feldspar series. This was first shown by the German mineralogist Johann Friedrich Christian Hessel (1796–1872) in 1826. The series ranges from albite to anorthite endmembers (with respective compositions NaAlSi3O8 to CaAl2Si2O8), where sodium and calcium atoms can substitute for each other in the mineral's crystal lattice structure. Plagioclase in hand samples is often identified by its polysynthetic crystal twinning or "record-groove" effect.

Plagioclase is a major constituent mineral in Earth's crust and is consequently an important diagnostic tool in petrology for identifying the composition, origin and evolution of igneous rocks. Plagioclase is also a major constituent of rock in the highlands of the Moon. Analysis of thermal emission spectra from the surface of Mars suggests that plagioclase is the most abundant mineral in the crust of Mars.

↑ Return to Menu

Crystal twinning in the context of Aragonite

Aragonite is a carbonate mineral and one of the three most common naturally occurring crystal forms of calcium carbonate (CaCO3), the others being calcite and vaterite. It is formed by biological and physical processes, including precipitation from marine and freshwater environments.

The crystal lattice of aragonite differs from that of calcite, resulting in a different crystal shape, an orthorhombic crystal system with acicular crystal. Repeated twinning results in pseudo-hexagonal forms. Aragonite may be columnar or fibrous, occasionally in branching helictitic forms called flos-ferri ("flowers of iron") from their association with the ores at the Carinthian iron mines.

↑ Return to Menu

Crystal twinning in the context of Cinnabar

Cinnabar (/ˈsɪnəˌbɑːr/; from Ancient Greek κιννάβαρι (kinnábari)), also called cinnabarite (/ˌsɪnəˈbɑːrt/) or mercurblende, is the bright scarlet to brick-red form of mercury(II) sulfide (HgS). It is the most common source ore for refining elemental mercury and is the historic source for the brilliant red or scarlet pigment termed vermilion and associated red mercury pigments.

Cinnabar generally occurs as a vein-filling mineral associated with volcanic activity and alkaline hot springs. The mineral resembles quartz in symmetry and it exhibits birefringence. Cinnabar has a mean refractive index near 3.2, a hardness between 2.0 and 2.5, and a specific gravity of approximately 8.1. The color and properties derive from a structure that is a hexagonal crystalline lattice belonging to the trigonal crystal system, crystals that sometimes exhibit twinning.

↑ Return to Menu

Crystal twinning in the context of Tin cry

Tin cry is the characteristic sound heard when a bar made of tin is bent. Variously described as a "screaming" or "crackling" sound, the effect is caused by the crystal twinning in the metal. The sound is not particularly loud, despite terms like "crying" and "screaming". It is very noticeable when a hot-dip tin-coated sheet metal is bent at high speed over rollers during processing.

Tin cry is often demonstrated using a simple science experiment. A bar of tin will "cry" repeatedly when bent until it breaks. The experiment can then be recycled by melting and recrystallizing the metal. The low melting point of tin, 231.9 °C (449.4 °F; 505.0 K), makes re-casting easy. Tin anneals at reasonably low temperature as well, normalizing tin's microstructure of crystallites/grains.

↑ Return to Menu

Crystal twinning in the context of Thin section

In optical mineralogy and petrography, a thin section (or petrographic thin section) is a thin slice of a rock or mineral sample, prepared in a laboratory, for use with a polarizing petrographic microscope, electron microscope and electron microprobe. A thin sliver of rock is cut from the sample with a diamond saw and ground optically flat. It is then mounted on a glass slide and then ground smooth using progressively finer abrasive grit until the sample is only 30 μm thick. The method uses the Michel-Lévy interference colour chart to determine thickness, typically using quartz as the thickness gauge because it is one of the most abundant minerals.

When placed between two polarizing filters set at right angles to each other, the optical properties of the minerals in the thin section alter the colour and intensity of the light as seen by the viewer. As different minerals have different optical properties, most rock-forming minerals can be easily identified. Plagioclase for example can be seen in the photo on the right as a clear mineral with multiple parallel twinning planes. The large blue-green minerals are clinopyroxene with some exsolution of orthopyroxene.

↑ Return to Menu

Crystal twinning in the context of Witherite

Witherite is a barium carbonate mineral, BaCO3, in the aragonite group. Witherite crystallizes in the orthorhombic system and virtually always is twinned. The mineral is colorless, milky-white, grey, pale-yellow, green, to pale-brown. The specific gravity is 4.3, which is high for a translucent mineral. It fluoresces light blue under both long- and short-wave UV light, and is phosphorescent under short-wave UV light.

Witherite forms in low-temperature hydrothermal environments. It is commonly associated with fluorite, celestine, galena, barite, calcite, and aragonite. Witherite occurrences include: Cave-in-Rock, Illinois, US; Pigeon Roost Mine, Glenwood, Arkansas, US; Settlingstones Mine Northumberland; Alston Moor, Cumbria; Anglezarke, Lancashire and Burnhope, County Durham, England; Thunder Bay area, Ontario, Canada, Germany, and Poland (Tarnowskie Góry and Tajno at Suwałki Region).

↑ Return to Menu

Crystal twinning in the context of Leucite

Leucite (from the Greek word leukos meaning white) is a rock-forming mineral of the feldspathoid group, silica-undersaturated and composed of potassium and aluminium tectosilicate KAlSi2O6. Crystals have the form of cubic icositetrahedra but, as first observed by Sir David Brewster in 1821, they are not optically isotropic, and are therefore pseudo-cubic. Goniometric measurements made by Gerhard vom Rath in 1873 led him to refer the crystals to the tetragonal system. Optical investigations have since proved the crystals to be still more complex in character, and to consist of several orthorhombic or monoclinic individuals, which are optically biaxial and repeatedly twinned, giving rise to twin-lamellae and to striations on the faces. When the crystals are raised to a temperature of about 500 °C they become optically isotropic and the twin-lamellae and striations disappear, although they reappear when the crystals are cooled again. This pseudo-cubic character of leucite is very similar to that of the mineral boracite. Leucite is commonly found in igneous rocks, especially at Mt. Vesuvius

The crystals are white or ash-grey in colour, hence the name suggested by A. G. Werner in 1701, from λευκος, '(matt) white'. They are transparent and glassy when fresh, albeit with a noticeably subdued 'subvitreous' lustre due to the low refractive index, but readily alter to become waxy/greasy and then dull and opaque; they are brittle and break with a conchoidal fracture. The Mohs hardness is 5.5, and the specific gravity 2.47. Inclusions of other minerals, arranged in concentric zones, are frequently present in the crystals. On account of the color and form of the crystals the mineral was early known as 'white garnet'. French authors in older literature may employ René Just Haüy's name amphigène, but 'leucite' is the only name for this mineral species that is recognised as official by the International Mineralogical Association.

↑ Return to Menu