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50-527: Other polymorphs of calcium carbonate are the minerals aragonite and vaterite . Aragonite will change to calcite over timescales of days or less at temperatures exceeding 300 °C, and vaterite is even less stable. Calcite is derived from the German Calcit , a term from the 19th century that came from the Latin word for lime , calx (genitive calcis ) with the suffix -ite used to name minerals. It

100-685: A = 10 Å and c = 8.5 Å , while the structural unit cell is hexagonal (i.e. a rhombic prism ), having approximate dimensions a = 5 Å and c = 17 Å . For the same orientation, c must be multiplied by 4 to convert from morphological to structural units. As an example, calcite cleavage is given as "perfect on {1 0 1 1}" in morphological coordinates and "perfect on {1 0 1 4}" in structural units. In { h k l } {\displaystyle \{hkl\}} indices, these are {1 0 1} and {1 0 4}, respectively. Twinning , cleavage and crystal forms are often given in morphological units. The diagnostic properties of calcite include

150-497: A calcium chloride solution to a sodium carbonate solution at temperatures above 60 °C (140 °F) or in water-ethanol mixtures at ambient temperatures. Aragonite is a thermodynamically unstable phase of calcium carbonate at any pressure below about 3,000 bars (300,000 kPa) at any temperature. Aragonite nonetheless frequently forms in near-surface environments at ambient temperatures. The weak Van der Waals forces inside aragonite give an important contribution to both

200-435: A dissolution and reprecipitation mechanism, with the reaction rate controlled by the surface area of a calcite crystal. The second stage of the reaction is approximately 10 times slower. However, crystallization of calcite has been observed to be dependent on the starting pH and concentration of magnesium in solution. A neutral starting pH during mixing promotes the direct transformation of ACC into calcite without

250-603: A clear piece of calcite to appear doubled. The birefringent effect (using calcite) was first described by the Danish scientist Rasmus Bartholin in 1669. At a wavelength of about 590 nm, calcite has ordinary and extraordinary refractive indices of 1.658 and 1.486, respectively. Between 190 and 1700 nm, the ordinary refractive index varies roughly between 1.9 and 1.5, while the extraordinary refractive index varies between 1.6 and 1.4. Calcite has thermoluminescent properties mainly due to manganese divalent ( Mn ). An experiment

300-421: A defining Mohs hardness of 3, a specific gravity of 2.71 and, in crystalline varieties, a vitreous luster . Color is white or none, though shades of gray, red, orange, yellow, green, blue, violet, brown, or even black can occur when the mineral is charged with impurities. Calcite has numerous habits, representing combinations of over 1000 crystallographic forms . Most common are scalenohedra , with faces in

350-403: A monohydrocalcite intermediate, sequestering carbon . Calcite is often the primary constituent of the shells of marine organisms , such as plankton (such as coccoliths and planktic foraminifera ), the hard parts of red algae , some sponges , brachiopods , echinoderms , some serpulids , most bryozoa , and parts of the shells of some bivalves (such as oysters and rudists ). Calcite

400-525: A vaterite intermediate. But when ACC forms in a solution with a basic initial pH, the transformation to calcite occurs via metastable vaterite, following the pathway outlined above. Magnesium has a noteworthy effect on both the stability of ACC and its transformation to crystalline CaCO 3 , resulting in the formation of calcite directly from ACC, as this ion destabilizes the structure of vaterite. Epitaxial overgrowths of calcite precipitated on weathered cleavage surfaces have morphologies that vary with

450-677: Is a carbonate mineral and one of the three most common naturally occurring crystal forms of calcium carbonate ( Ca CO 3 ), 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

500-445: Is considered essential for the replication of reef conditions. Aragonite provides the materials necessary for much sea life and also keeps the pH of the water close to its natural level, to prevent the dissolution of biogenic calcium carbonate . Aragonite has been successfully tested for the removal of pollutants like zinc , cobalt and lead from contaminated wastewaters. Crystal habit In mineralogy , crystal habit

550-438: Is designed to promote sustainable development in the mining industry. Calcite can help synthesize precipitated calcium carbonate (PCC) (mainly used in the paper industry) and increase carbonation . Furthermore, due to its particular crystal habit, such as rhombohedron, hexagonal prism, etc., it promotes the production of PCC with specific shapes and particle sizes. Calcite, obtained from an 80 kg sample of Carrara marble ,

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600-434: Is divided into low-magnesium and high-magnesium calcite, with the dividing line placed at a composition of 4% magnesium. High-magnesium calcite retains the calcite mineral structure, which is distinct from that of dolomite , MgCa(CO 3 ) 2 . Calcite can also contain small quantities of iron and manganese . Manganese may be responsible for the fluorescence of impure calcite, as may traces of organic compounds. Calcite

650-738: Is found all over the world, and its leading global distribution is as follows: Calcite is found in many different areas in the United States. One of the best examples is the Calcite Quarry in Michigan. The Calcite Quarry is the largest carbonate mine in the world and has been in use for more than 85 years. Large quantities of calcite can be mined from these sizeable open pit mines. Calcite can also be found throughout Canada, such as in Thorold Quarry and Madawaska Mine, Ontario, Canada. Abundant calcite

700-471: Is found in spectacular form in the Snowy River Cave of New Mexico as mentioned above, where microorganisms are credited with natural formations. Trilobites , which became extinct a quarter billion years ago , had unique compound eyes that used clear calcite crystals to form the lenses. It also forms a substantial part of birds' eggshells, and the δC of the diet is reflected in the δC of the calcite of

750-521: Is known as lublinite . Cleavage is usually in three directions parallel to the rhombohedron form. Its fracture is conchoidal , but difficult to obtain. Scalenohedral faces are chiral and come in pairs with mirror-image symmetry; their growth can be influenced by interaction with chiral biomolecules such as L- and D- amino acids . Rhombohedral faces are not chiral. Calcite is transparent to opaque and may occasionally show phosphorescence or fluorescence . A transparent variety called " Iceland spar "

800-751: Is mined in the Santa Eulalia mining district, Chihuahua, Mexico. Large quantities of calcite in Iceland are concentrated in the Helgustadir mine . The mine was once the primary mining location of "Iceland spar." However, it currently serves as a nature reserve, and calcite mining will not be allowed. Calcite is found in parts of England, such as Alston Moor, Egremont, and Frizington, Cumbria. St. Andreasberg, Harz Mountains, and Freiberg, Saxony can find calcite. Ancient Egyptians carved many items out of calcite, relating it to their goddess Bast , whose name contributed to

850-552: Is one of the minerals that has been shown to catalyze an important biological reaction, the formose reaction , and may have had a role in the origin of life. Interaction of its chiral surfaces (see Form ) with aspartic acid molecules results in a slight bias in chirality; this is one possible mechanism for the origin of homochirality in living cells. Climate change is exacerbating ocean acidification , possibly leading to lower natural calcite production. The oceans absorb large amounts of CO 2 from fossil fuel emissions into

900-423: Is the characteristic external shape of an individual crystal or aggregate of crystals. The habit of a crystal is dependent on its crystallographic form and growth conditions, which generally creates irregularities due to limited space in the crystallizing medium (commonly in rocks ). Recognizing the habit can aid in mineral identification and description, as the crystal habit is an external representation of

950-431: Is the first to form. The presence of magnesium ions may inhibit calcite formation in favor of aragonite. Once formed, aragonite tends to alter to calcite on scales of 10 to 10 years. The mineral vaterite , also known as μ-CaCO 3 , is another phase of calcium carbonate that is metastable at ambient conditions typical of Earth's surface, and decomposes even more readily than aragonite. In aquaria , aragonite

1000-401: Is the leading cause of excessive growth of cyanobacteria. As an active capping material, calcite can help reduce P release from sediments into the water, thus inhibiting cyanobacteria overgrowth. Calcite is a common constituent of sedimentary rocks , limestone in particular, much of which is formed from the shells of dead marine organisms. Approximately 10% of sedimentary rock is limestone. It

1050-474: Is the primary mineral in metamorphic marble . It also occurs in deposits from hot springs as a vein mineral; in caverns as stalactites and stalagmites ; and in volcanic or mantle-derived rocks such as carbonatites , kimberlites , or rarely in peridotites . Cacti contain Ca-oxalate biominerals. Their death releases these biominerals into the environment, which subsequently transform to calcite via

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1100-515: Is thus a doublet of the word chalk . When applied by archaeologists and stone trade professionals, the term alabaster is used not just as in geology and mineralogy, where it is reserved for a variety of gypsum ; but also for a similar-looking, translucent variety of fine-grained banded deposit of calcite. In publications, two different sets of Miller indices are used to describe directions in hexagonal and rhombohedral crystals, including calcite crystals: three Miller indices h, k, l in

1150-581: Is used as the IAEA -603 isotopic standard in mass spectrometry for the calibration of δO and δC . Calcite can be formed naturally or synthesized. However, artificial calcite is the preferred material to be used as a scaffold in bone tissue engineering due to its controllable and repeatable properties. Calcite can be used to alleviate water pollution caused by the excessive growth of cyanobacteria . Lakes and rivers can lead to cyanobacteria blooms due to eutrophication , which pollutes water resources. Phosphorus (P)

1200-521: Is used for optical purposes. Acute scalenohedral crystals are sometimes referred to as "dogtooth spar" while the rhombohedral form is sometimes referred to as "nailhead spar". The rhombohedral form may also have been the " sunstone " whose use by Viking navigators is mentioned in the Icelandic Sagas . Single calcite crystals display an optical property called birefringence (double refraction). This strong birefringence causes objects viewed through

1250-448: The a 1 , a 2 , c {\displaystyle a_{1},a_{2},c} directions, or four Bravais–Miller indices h, k, i, l in the a 1 , a 2 , a 3 , c {\displaystyle a_{1},a_{2},a_{3},c} directions, where i {\displaystyle i} is redundant but useful in visualizing permutation symmetries . To add to

1300-831: The Ochtinská Aragonite Cave , is situated in Slovakia . In the US, aragonite in the form of stalactites and "cave flowers" ( anthodite ) is known from Carlsbad Caverns and other caves. For a few years in the early 1900s, aragonite was mined at Aragonite, Utah (now a ghost town). Massive deposits of oolitic aragonite sand are found on the seabed in the Bahamas . Aragonite is the high pressure polymorph of calcium carbonate . As such, it occurs in high pressure metamorphic rocks such as those formed at subduction zones . Aragonite forms naturally in almost all mollusk shells, and as

1350-463: The calcareous endoskeleton of warm- and cold-water corals ( Scleractinia ). Several serpulids have aragonitic tubes. Because the mineral deposition in mollusk shells is strongly biologically controlled, some crystal forms are distinctively different from those of inorganic aragonite. In some mollusks, the entire shell is aragonite; in others, aragonite forms only discrete parts of a bimineralic shell (aragonite plus calcite). The nacreous layer of

1400-494: The internal ordered atomic arrangement . Most natural crystals, however, do not display ideal habits and are commonly malformed. Hence, it is also important to describe the quality of the shape of a mineral specimen: Factors influencing habit include: a combination of two or more crystal forms; trace impurities present during growth; crystal twinning and growth conditions (i.e., heat, pressure, space); and specific growth tendencies such as growth striations . Minerals belonging to

1450-792: The ores at the Carinthian iron mines. The type location for aragonite is Molina de Aragón in the Province of Guadalajara in Castilla-La Mancha , Spain , for which it was named in 1797. Aragonite is found in this locality as cyclic twins inside gypsum and marls of the Keuper facies of the Triassic . This type of aragonite deposit is very common in Spain, and there are also some in France. An aragonite cave,

1500-643: The air. The total amount of artificial CO 2 absorbed by the oceans is calculated to be 118 ± 19 Gt C. If a large amount of CO 2 dissolves in the sea, it will cause the acidity of the seawater to increase, thereby affecting the pH value of the ocean. Calcifying organisms in the sea, such as molluscs foraminifera, crustaceans, echinoderms and corals, are susceptible to pH changes. Meanwhile, these calcifying organisms are also an essential source of calcite. As ocean acidification causes pH to drop, carbonate ion concentrations will decline, potentially reducing natural calcite production. Aragonite Aragonite

1550-458: The aragonite fossil shells of some extinct ammonites forms an iridescent material called ammolite . Aragonite also forms naturally in the endocarp of Celtis occidentalis . The skeleton of some calcareous sponges is made of aragonite. Aragonite also forms in the ocean inorganic precipitates called marine cements (in the sediment ) or as free crystals (in the water column). Inorganic precipitation of aragonite in caves can occur in

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1600-470: The classical terrace ledge kink model to the crystallization of poorly ordered precursor phases like amorphous calcium carbonate (ACC) via an Ostwald ripening process, or via the agglomeration of nanocrystals. The crystallization of ACC can occur in two stages. First, the ACC nanoparticles rapidly dehydrate and crystallize to form individual particles of vaterite . Second, the vaterite transforms to calcite via

1650-411: The complications, there are also two definitions of unit cell for calcite. One, an older "morphological" unit cell, was inferred by measuring angles between faces of crystals, typically with a goniometer , and looking for the smallest numbers that fit. Later, a "structural" unit cell was determined using X-ray crystallography . The morphological unit cell is rhombohedral , having approximate dimensions

1700-461: The crystallographic and elastic properties of this mineral. The difference in stability between aragonite and calcite, as measured by the Gibbs free energy of formation , is small, and effects of grain size and impurities can be important. The formation of aragonite at temperatures and pressures where calcite should be the stable polymorph may be an example of Ostwald's step rule , where a less stable phase

1750-435: The expansion and eventual collapse of cave systems, resulting in various forms of karst topography . Calcite exhibits an unusual characteristic called retrograde solubility: it is less soluble in water as the temperature increases. Calcite is also more soluble at higher pressures. Pure calcite has the composition CaCO 3 . However, the calcite in limestone often contains a few percent of magnesium . Calcite in limestone

1800-484: The following reaction The carbon dioxide released by this reaction produces a characteristic effervescence when a calcite sample is treated with an acid. Due to its acidity, carbon dioxide has a slight solubilizing effect on calcite. The overall reaction is If the amount of dissolved carbon dioxide drops, the reaction reverses to precipitate calcite. As a result, calcite can be either dissolved by groundwater or precipitated by groundwater, depending on such factors as

1850-509: The form of speleothems . Aragonite is common in serpentinites where magnesium-rich pore solutions apparently inhibit calcite growth and promote aragonite precipitation. Aragonite is metastable at the low pressures near the Earth's surface and is thus commonly replaced by calcite in fossils. Aragonite older than the Carboniferous is essentially unknown. Aragonite can be synthesized by adding

1900-724: The glow curve peaks, it was found that Pb and Mn acted as activators in the calcite lattice, but Pb was much less efficient than Mn . Measuring mineral thermoluminescence experiments usually use x-rays or gamma-rays to activate the sample and record the changes in glowing curves at a temperature of 700–7500 K. Mineral thermoluminescence can form various glow curves of crystals under different conditions, such as temperature changes, because impurity ions or other crystal defects present in minerals supply luminescence centers and trapping levels. Observing these curve changes also can help infer geological correlation and age determination. Calcite, like most carbonates, dissolves in acids by

1950-463: The hexagonal {2 1 1} directions (morphological unit cell) or {2 1 4} directions (structural unit cell); and rhombohedral, with faces in the {1 0 1} or {1 0 4} directions (the most common cleavage plane). Habits include acute to obtuse rhombohedra, tabular habits, prisms , or various scalenohedra . Calcite exhibits several twinning types that add to the observed habits. It may occur as fibrous, granular, lamellar, or compact. A fibrous, efflorescent habit

2000-424: The ocean at the time they became mineralised, and retained this mineralogy for the remainder of their evolutionary history. Petrographic evidence for these calcite sea conditions consists of calcitic ooids , lmc cements, hardgrounds , and rapid early seafloor aragonite dissolution. The evolution of marine organisms with calcium carbonate shells may have been affected by the calcite and aragonite sea cycle. Calcite

2050-514: The primary inorganic precipitate of calcium carbonate in marine waters was low-magnesium calcite (lmc), as opposed to the aragonite and high-magnesium calcite (hmc) precipitated today. Calcite seas alternated with aragonite seas over the Phanerozoic , being most prominent in the Ordovician and Jurassic periods. Lineages evolved to use whichever morph of calcium carbonate was favourable in

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2100-504: The same 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, those found in Montana form stout tabular crystals. Ordinarily, the latter habit is seen only in ruby . Sapphire and ruby are both varieties of the same mineral: corundum . Some minerals may replace other existing minerals while preserving

2150-671: The shell. The largest documented single crystal of calcite originated from Iceland, measured 7 m × 7 m × 2 m (23 ft × 23 ft × 6.6 ft) and 6 m × 6 m × 3 m (20 ft × 20 ft × 9.8 ft) and weighed about 250 tons. Classic samples have been produced at Madawaska Mine , near Bancroft, Ontario . Bedding parallel veins of fibrous calcite, often referred to in quarrying parlance as beef , occur in dark organic rich mudstones and shales, these veins are formed by increasing fluid pressure during diagenesis . Calcite formation can proceed by several pathways, from

2200-431: The sky through the crystal and then rotating it so that the two images are of equal brightness, the rings of polarized light that surround the sun can be seen even under overcast skies. Identifying the sun's location would give seafarers a reference point for navigating on their lengthy sea voyages. In World War II, high-grade optical calcite was used for gun sights, specifically in bomb sights and anti-aircraft weaponry. It

2250-498: The subsurface in response to microorganism activity, such as sulfate -dependent anaerobic oxidation of methane , where methane is oxidized and sulfate is reduced , leading to precipitation of calcite and pyrite from the produced bicarbonate and sulfide . These processes can be traced by the specific carbon isotope composition of the calcites, which are extremely depleted in the C isotope, by as much as −125 per mil PDB (δC). Calcite seas existed in Earth's history when

2300-416: The term alabaster because of the close association. Many other cultures have used the material for similar carved objects and applications. A transparent variety of calcite known as Iceland spar may have been used by Vikings for navigating on cloudy days. A very pure crystal of calcite can split a beam of sunlight into dual images, as the polarized light deviates slightly from the main beam. By observing

2350-456: The type of weathering the substrate experienced: growth on physically weathered surfaces has a shingled morphology due to Volmer-Weber growth, growth on chemically weathered surfaces has characteristics of Stranski-Krastanov growth, and growth on pristine cleavage surfaces has characteristics of Frank - van der Merwe growth. These differences are apparently due to the influence of surface roughness on layer coalescence dynamics. Calcite may form in

2400-495: The water temperature, pH , and dissolved ion concentrations. When conditions are right for precipitation, calcite forms mineral coatings that cement rock grains together and can fill fractures. When conditions are right for dissolution, the removal of calcite can dramatically increase the porosity and permeability of the rock, and if it continues for a long period of time, may result in the formation of caves . Continued dissolution of calcium carbonate-rich formations can lead to

2450-415: Was conducted by adding activators such as ions of Mn, Fe, Co, Ni, Cu, Zn, Ag, Pb, and Bi to the calcite samples to observe whether they emitted heat or light. The results showed that adding ions ( Cu , Cu , Zn , Ag , Bi , Fe , Fe , Co , Ni ) did not react. However, a reaction occurred when both manganese and lead ions were present in calcite. By changing the temperature and observing

2500-451: Was used as a polarizer (in Nicol prisms ) before the invention of Polaroid plates and still finds use in optical instruments. Also, experiments have been conducted to use calcite for a cloak of invisibility . Microbiologically precipitated calcite has a wide range of applications, such as soil remediation, soil stabilization and concrete repair. It also can be used for tailings management and

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