domingo, 21 de julho de 2013

Rhodonite

Rhodonite


Rhodonite
Rodonita2EZ.jpg
Rhodonite crystals in rock
General
Category Inosilicate
Formula
(repeating unit)
(Mn2+,Fe2+,Mg,Ca)SiO3
Strunz classification 09.DK.05
Dana classification 65.04.01.01
Crystal symmetry Triclinic 1 pinacoidal
Unit cell a = 9.758 Å, b = 10.499 Å, c = 12.205 Å; α = 108.58°, β = 102.92°, γ = 82.52°; Z = 20
Identification
Color Rose-pink to brownish red, gray, or yellow
Crystal habit Tabular crystals, massive, granular
Crystal system Triclinic - Pinacoidal H-M Symbol (1) Space Group: P1
Twinning Lamellar, composition plane {010}
Cleavage Perfect on {110} and {110}, (110) ^ (110) = 92.5°; good on {001}
Fracture Conchoidal to uneven
Mohs scale hardness 5.5 - 6.5
Luster Vitreous to pearly
Streak White
Diaphaneity Transparent to translucent
Specific gravity 3.57 - 3.76
Optical properties Biaxial (+)
Refractive index nα = 1.711 - 1.738 nβ = 1.714 - 1.741 nγ = 1.724 - 1.751
Birefringence δ = 0.013
Pleochroism Weak
2V angle Measured: 58° to 73°, Calculated: 58°
Alters to Exterior commonly black from manganese oxides
References [1][2][3]
Rhodonite is a manganese inosilicate, (Mn, Fe, Mg, Ca)SiO3 and member of the pyroxenoid group of minerals, crystallizing in the triclinic system. It commonly occurs as cleavable to compact masses with a rose-red color (the name comes from the Greek ῥόδος rhodos, rosy), often tending to brown because of surface oxidation.
Rhodonite crystals often have a thick tabular habit, but are rare. It has a perfect, prismatic cleavage, almost at right angles. The hardness is 5.5–6.5, and the specific gravity 3.4–3.7; luster is vitreous, being less frequently pearly on cleavage surfaces. The manganese is often partly replaced by iron, magnesium, calcium, and sometimes zinc which may sometimes be present in considerable amounts; a greyish-brown variety containing as much as 20% of calcium oxide is called bustamite; fowlerite is a zinciferous variety containing 7% of zinc oxide.
Pink rhodonite contrasting with black manganese oxides is sometimes used as gemstone material as seen in this specimen from Humboldt County, Nevada.
The inosilicate (chain silicate) structure of rhodonite has a repeat unit of five silica tetrahedra. The rare polymorph pyroxmangite, formed at different conditions of pressure and temperature, has the same chemical composition but a repeat unit of seven tetrahedra.
Rhodonite has also been worked as an ornamental stone. In the iron and manganese mines at Pajsberg near Filipstad and Långban in Värmland, Sweden, small brilliant and translucent crystals (pajsbergite) and cleavage masses occur. Fowlerite occurs as large, rough crystals, somewhat resembling pink feldspar, with franklinite and zinc ores in granular limestone at Franklin Furnace in New Jersey.
Rhodonite is the official gem of Commonwealth of Massachusetts.[4]
Brazil

See also

References

  1. ^ Handbook of Mineralogy
  2. ^ Rhodonite, Mindat.org
  3. ^ Rhodonite, Webmineral data
  4. ^ General Laws of Massachusetts, Chapter 2, Section 15.
Public Domain This article incorporates text from a publication now in the public domainChisholm, Hugh, ed. (1911). Encyclopædia Britannica (11th ed.). Cambridge University Press.
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Dolomite

Dolomite


Dolomite
Dolomite-Magnésite- Navarre.jpg
Dolomite and magnesite – Spain
General
Category Carbonate mineral
Formula
(repeating unit)
(CaMg)(CO3)2
Strunz classification 05.AB.10
Crystal symmetry Trigonal rhombohedral, 3
Unit cell a = 4.8012(1) Å, c = 16.002 Å; Z = 3
Identification
Color White, gray to pink
Crystal habit Tabular crystals, often with curved faces, also columnar, stalactitic, granular, massive.
Crystal system Trigonal
Twinning Common as simple contact twins
Cleavage Perfect on {1011}, rhombohedral cleavage
Fracture Conchoidal
Tenacity Brittle
Mohs scale hardness 3.5 to 4
Luster Vitreous to pearly
Streak White
Specific gravity 2.84–2.86
Optical properties Uniaxial (-)
Refractive index nω = 1.679–1.681 nε = 1.500
Birefringence δ = 0.179–0.181
Solubility Poorly soluble in dilute HCl unless powdered.
Other characteristics May fluoresce white to pink under UV; triboluminescent.
References [1][2][3][4]
Dolomite /ˈdɒləmt/ is a carbonate mineral composed of calcium magnesium carbonate CaMg(CO3)2. The term is also used to describe the sedimentary carbonate rock dolostone.
Dolostone (dolomite rock) is composed predominantly of the mineral dolomite with a stoichiometric ratio of 50% or greater content of magnesium replacing calcium, often as a result of diagenesis. Limestone that is partially replaced by dolomite is referred to as dolomitic limestone, or in old U.S. geologic literature as magnesian limestone.

Contents

History

Dolomite was first described by the Austrian naturalist Belsazar Hacquet as the "stinking stone" (German: Stinkstein, Latin: lapis suillus in 1778).[5][6] In 1791, it was described as a rock by the French naturalist and geologist, Déodat Gratet de Dolomieu (1750–1801) from exposures in what are now known as the Dolomite Alps of northern Italy. The mineral was given its name in March 1792 by Nicolas de Saussure.[7] Hacquet and Dolomieu met in Laibach (Ljubljana) in 1784,[8] which may have contributed to Dolomieu's work.[6]

Properties

The mineral dolomite crystallizes in the trigonal-rhombohedral system. It forms white, gray to pink, commonly curved (saddle shape) crystals, although it is usually massive. Unlike calcite, dolomite is a double carbonate, having a different structural arrangement, and it does not rapidly dissolve or effervesce (fizz) in dilute hydrochloric acid unless it is scratched or in powdered form. Crystal twinning is common. A solid solution series exists between dolomite and iron rich ankerite. Small amounts of iron in the structure give the crystals a yellow to brown tint. Manganese substitutes in the structure also up to about three percent MnO. A high manganese content gives the crystals a rosy pink color noted in the image above. A series with the manganese rich kutnohorite may exist. Lead and zinc also substitute in the structure for magnesium. It is also related to huntite Mg3Ca(CO3)4.

Formation

Vast deposits are present in the geological record, but the mineral is relatively rare in modern environments. Laboratory synthesis of stoichiometric dolomite has been carried out only at temperatures of greater than 100 °C (conditions typical of burial in sedimentary basins), even though much dolomite in the rock record appears to have formed in low-temperature conditions. The high temperature is likely to speed up the movement of calcium and magnesium ions so that they can find their places in the ordered structure within a reasonable amount of time. This suggests that the lack of dolomite that is being formed today is likely due to kinetic factors, i.e. due to the lack of kinetic energy or temperature.
Dolomite druse from Lawrence County, Arkansas, USA (size: 24×18×8 cm)
Modern dolomite does occur as a precipitating mineral in specialized environments on the surface of the earth today. In the 1950s and 60s, dolomite was found to be forming in highly saline lakes in the Coorong region of South Australia. Dolomite crystals also occur in deep-sea sediments, where organic matter content is high. This dolomite is termed "organogenic" dolomite.
Recent research has found modern dolomite formation under anaerobic conditions in supersaturated saline lagoons along the Rio de Janeiro coast of Brazil, namely, Lagoa Vermelha and Brejo do Espinho. One interesting reported case was the formation of dolomite in the kidneys of a Dalmatian dog.[9] This was believed to be due to chemical processes triggered by bacteria. Dolomite has been speculated to develop under these conditions with the help of sulfate-reducing bacteria (e.g. Desulfovibrio brasiliensis).[10][11]
Dolomite.
The actual role of bacteria in the low-temperature formation of dolomite remains to be demonstrated. The specific mechanism of dolomitization, involving sulfate-reducing bacteria, has not yet been demonstrated.[12]
Dolomite appears to form in many different types of environment and can have varying structural, textural and chemical characteristics. Some researchers have stated "there are dolomites and dolomites", meaning that there may not be one single mechanism by which dolomite can form. Much modern dolomite differs significantly from the bulk of the dolomite found in the rock record, leading researchers to speculate that environments where dolomite formed in the geologic past differ significantly from those where it forms today.
Dolomite bedrock underneath a Bristlecone Pine, White Mountains, California.
Reproducible laboratory syntheses of dolomite (and magnesite) leads first to the initial precipitation of a metastable "precursor" (such as magnesium calcite), to be changed gradually into more and more of the stable phase (such as dolomite or magnesite) during periodical intervals of dissolution and reprecipitation. The general principle governing the course of this irreversible geochemical reaction has been coined Ostwald's step rule.
For a very long time scientists had difficulties synthesizing dolomite. However, in a 1999 study, through a process of dissolution alternating with intervals of precipitation, measurable levels of dolomite were synthesized at low temperatures and pressures.[13]

Coral atolls

Dolomitization of calcite also occurs at certain depths of coral atolls where water is undersaturated in calcium carbonate but saturated in dolomite. Convection created by tides and sea currents enhance this change. Hydrothermal currents created by volcanoes under the atoll may also play an important role.

Uses

Dolomite with chalcopyrite from the Tri-state district, Cherokee County, Kansas (size: 11.4×7.2×4.6 cm)
Dolomite is used as an ornamental stone, a concrete aggregate, a source of magnesium oxide and in the Pidgeon process for the production of magnesium. It is an important petroleum reservoir rock, and serves as the host rock for large strata-bound Mississippi Valley-Type (MVT) ore deposits of base metals such as lead, zinc, and copper. Where calcite limestone is uncommon or too costly, dolomite is sometimes used in its place as a flux for the smelting of iron and steel. Large quantities of processed dolomite are used in the production of float glass.
In horticulture, dolomite and dolomitic limestone are added to soils and soilless potting mixes as a pH buffer and as a magnesium source. Home and container gardening are common examples of this use.
Dolomite is also used as the substrate in marine (saltwater) aquariums to help buffer changes in pH of the water.
Particle physics researchers prefer to build particle detectors under layers of dolomite to enable the detectors to detect the highest possible number of exotic particles. Because dolomite contains relatively minor quantities of radioactive materials, it can insulate against interference from cosmic rays without adding to background radiation levels.[14]

See also

References

  1. ^ Deer, W. A., R. A. Howie and J. Zussman (1966) An Introduction to the Rock Forming Minerals, Longman, pp. 489–493. ISBN 0-582-44210-9.
  2. ^ Dolomite. Handbook of Mineralogy. (PDF) . Retrieved on 2011-10-10.
  3. ^ Dolomite. Webmineral. Retrieved on 2011-10-10.
  4. ^ Dolomite. Mindat.org. Retrieved on 2011-10-10.
  5. ^ Felizardo, Alexandre. "Baltazar Hacquet (1739–1815)". Cavernas em Foco (in Spanish). Bookess. p. 119. ISBN 9788562418938.
  6. ^ a b Kranjc, Andrej (2006). "Balthasar Hacquet (1739/40-1815), the Pionneer of Karst Geomorphologists". Acta Carsologica (Institute for the Karst Research, Scientific Research Centre, Slovenian Academy of Sciences and Arts) 35 (2). ISSN 0583-6050.
  7. ^ Gardien, Guy (2002). "Introduction". Déodat Gratet de Dolomieu (in French). Editions Publibook. p. 9. ISBN 9782748312386.
  8. ^ Šumrada, Janez (2001). "Žiga Zois in Déodat de Dolomieu". Kronika: časopis za slovensko krajevno zgodovino [The Chronicle: the Newspaper for the Slovenian History of Places] (in Slovene, with an English abstract) (Association of Slovenian Historical Societies, Section for the History of Places) 49 (1/2): 65–72. ISSN 0023-4923.
  9. ^ Mansfield, Charles F. (1980). "A urolith of biogenic dolomite – another clue in the dolomite mystery". Geochimica et Cosmochimica Acta 44 (6): 829–839. Bibcode:1980GeCoA..44..829M. doi:10.1016/0016-7037(80)90264-1.
  10. ^ Vasconcelos C., McKenzie J. A., Bernasconi S., Grujic D., Tien A. J. (1995). "Microbial mediation as a possible mechanism for natural dolomite formation at low temperatures". Nature 337: 220–222. doi:10.1038/377220a0.
  11. ^ Warthmann R., van Lith Y., Vasconcelos C., McKenzie J. A., Karpoff A. M. (2000). "Bacterially induced dolomite precipitation in anoxic culture experiments". Geology 28: 1091–1094. doi:10.1130/0091-7613(2000)28<1091:BIDPIA>2.0.CO;2.
  12. ^ Yvonne van Lith et al. (2000). "Role of Sulfate Reducing Bacteria During Microbial Dolomite Precipitation as Deduced from Culture Experiments". Journal of Conference Abstracts 5 (2): 1038.
  13. ^ Deelman, J.C. (1999): "Low-temperature nucleation of magnesite and dolomite", Neues Jahrbuch für Mineralogie, Monatshefte, pp. 289–302.
  14. ^ Short Sharp Science: Particle quest: Hunting for Italian WIMPs underground. Newscientist.com (2011-09-05). Retrieved on 2011-10-10.

Agate

Agate


Agate
Agate banded 750pix.jpg
Banded agate (agate-like onyx); the specimen is 2.5 cm (1 inch) wide
General
Category Quartz variety
Formula
(repeating unit)
SiO2 silicon dioxide
Identification
Color White to grey, light blue, orange to red, black. banded
Crystal habit Cryptocrystalline silica
Crystal system Rhombohedral Microcrystalline
Cleavage None
Fracture Conchoidal with very sharp edges.
Mohs scale hardness 6.5–7
Luster Waxy
Streak White
Diaphaneity Translucent
Specific gravity 2.58–2.64
Refractive index 1.530–1.540
Birefringence up to +0.004 (B-G)
Pleochroism Absent
Agate /ˈæɡət/ is a microcrystalline variety of silica, chiefly chalcedony, characterised by its fineness of grain and brightness of color. Although agates may be found in various kinds of rock, they are classically associated with volcanic rocks and can be common in certain metamorphic rocks.[1]

Contents

Etymology and history

The stone was given its name by Theophrastus, a Greek philosopher and naturalist, who discovered the stone along the shore line of the river Achates (Greek: Ἀχάτης) sometime between the 4th and 3rd centuries BC.[2] Colorful agates and other chalcedonies were obtained over 3,000 years ago from the Achates River, now called Dirillo, in Sicily.[3]

Ancient use

Agate is one of the most common materials used in the art of hardstone carving, and has been recovered at a number of ancient sites, indicating its widespread use in the ancient world; for example, archaeological recovery at the Knossos site on Crete illustrates its role in Bronze Age Minoan culture.[4]

Formation and characteristics

Botswana agate
Most agates occur as nodules in volcanic rocks or ancient lavas where they represent cavities originally produced by the disengagement of volatiles in the molten mass which were then filled, wholly or partially, by siliceous matter deposited in regular layers upon the walls. Agate has also been known to fill veins or cracks in volcanic or altered rock underlain by granitic intrusive masses. Such agates, when cut transversely, exhibit a succession of parallel lines, often of extreme tenuity, giving a banded appearance to the section. Such stones are known as banded agate, riband agate and striped agate.
In the formation of an ordinary agate, it is probable that waters containing silica in solution—derived, perhaps, from the decomposition of some of the silicates in the lava itself—percolated through the rock and deposited a siliceous coating on the interior of the vapour-vesicles. Variations in the character of the solution or in the conditions of deposition may cause a corresponding variation in the successive layers, so that bands of chalcedony often alternate with layers of crystalline quartz. Several vapour-vesicles may unite while the rock is still viscous, and thus form a large cavity which may become the home of an agate of exceptional size; thus a Brazilian geode lined with amethyst and weighing 35 tons was exhibited at the Düsseldorf Exhibition of 1902. Perhaps the most comprehensive review of agate chemistry is a recent text by Moxon cited below.
The first deposit on the wall of a cavity, forming the "skin" of the agate, is generally a dark greenish mineral substance, like celadonite, delessite or "green earth", which are rich in iron probably derived from the decomposition of the augite in the enclosing volcanic rock. This green silicate may give rise by alteration to a brown iron oxide (limonite), producing a rusty appearance on the outside of the agate-nodule. The outer surface of an agate, freed from its matrix, is often pitted and rough, apparently in consequence of the removal of the original coating. The first layer spread over the wall of the cavity has been called the "priming", and upon this base zeolitic minerals may be deposited.
Many agates are hollow, since deposition has not proceeded far enough to fill the cavity, and in such cases the last deposit commonly consists of drusy quartz, sometimes amethystine, having the apices of the crystals directed towards the free space so as to form a crystal-lined cavity or geode.
On the disintegration of the matrix in which the agates are embedded, they are set free. The agates are extremely resistant to weathering and remain as nodules in the soil or are deposited as gravel in streams and shorelines.

Types of agate

Agatized Coral
"Turritella agate" (Elimia tenera) from Green River Formation, Wyoming
A Mexican agate, showing only a single eye, has received the name of cyclops agate. Included matter of a green, golden, red, black or other color or combinations embedded in the chalcedony and disposed in filaments and other forms suggestive of vegetable growth, gives rise to dendritic or moss agate. Dendritic agates have fern like patterns in them formed due to the presence of manganese and iron oxides. Other types of included matter deposited during agate-building include sagenitic growths (radial mineral crystals) and chunks of entrapped detritus (such as sand, ash, or mud). Occasionally agate fills a void left by decomposed vegetative material such as a tree limb or root and is called limb cast agate due to its appearance.
Turritella agate is formed from silicified fossil Elimia tenera (erroneously considered Turritella) shells. E. tenera are spiral freshwater gastropods having elongated, spiral shells composed of many whorls. Similarly, coral, petrified wood and other organic remains or porous rocks can also become agatized. Agatized coral is often referred to as Petoskey stone or agate.
Greek agate is a name given to pale white to tan colored agate found in Sicily back to 400 B.C. The Greeks used it for making jewelry and beads. Even though the stone had been around centuries and was known to both the Sumerians and the Egyptians, both who used the gem for decoration and for playing important parts in their religious ceremonies, any agate of this color from Sicily, once an ancient Greek colony, is called Greek agate.
Another type of agate is Brazilian agate, which is found as sizable geodes of layered nodules. These occur in brownish tones interlayered with white and gray. Quartz forms within these nodules, creating a striking specimen when cut opposite the layered growth axis. It is often dyed in various colors for ornamental purposes.
Certain stones, when examined in thin sections by transmitted light, show a diffraction spectrum due to the extreme delicacy of the successive bands, whence they are termed rainbow agates. Often agate coexists with layers or masses of opal, jasper or crystalline quartz due to ambient variations during the formation process.
Other forms of agate include Lake Superior agate, carnelian agate (exhibiting reddish hues), Botswana agate, blue lace agate, plume agates, moss agate, tube agate (with visible flow channels or pinhole-sized 'tubes'), fortification agate (which exhibit little or no banding structure), fire agate (which has internal flash or 'fire', the result of a layer of clear agate over a layer of hydrothermally-deposited hematite), Mexican crazy-lace agate, which often exhibits a brightly colored, complexly banded pattern (also called Rodeo Agate and Rosetta Stone depending on who owned the mine at the time).
The "Rubens Vase" (Byzantine Empire). Carved in high relief from a single piece of agate, this extraordinary vase was most likely created in an imperial workshop for a Byzantine emperor.

Uses in industry and art

Industry uses agates chiefly to make ornaments such as pins, brooches or other types of jewelry, paper knives, inkstands, marbles and seals. Agate is also still used today for decorative displays, cabochons, beads, carvings and Intarsia art as well as face-polished and tumble-polished specimens of varying size and origin. Because of its hardness and ability to resist acids, agate is used to make mortars and pestles to crush and mix chemicals. Because of the high polish possible with agate it has been used for centuries for leather burnishing tools. Idar-Oberstein was one of the centers which made use of agate on an industrial scale. Where in the beginning locally found agates were used to make all types of objects for the European market, this became a globalized business around the turn of the 20th century: Idar-Oberstein imported large quantities of agate from Brazil, as ship's ballast. Making use of a variety of proprietary chemical processes, they produced colored beads that were sold around the globe.[5] Agates have long been used in arts and crafts. The sanctuary of a Presbyterian church in Yachats, Oregon, has six windows with panes made of agates collected from the local beaches.[6]
A 15-pound tumbler barrel full of glistening tumble-polished agate and jasper.

See also

Notes

  1. ^ Donald W. Hyndman, David D. Alt (2002). Roadside Geology of Oregon (18th ed.). Missoula, Montana: Mountain Press Publishing Company. p. 286. ISBN 0-87842-063-0.
  2. ^ Achates, Henry George Liddell, Robert Scott, A Greek-English Lexicon, at Perseus
  3. ^ "Agate Creek Agate". Archived from the original on 16 July 2007. Retrieved 2007-07-01.
  4. ^ C. Michael Hogan. 2007. Knossos fieldnotes, Modern Antiquarian
  5. ^ Background Article on Idar Oberstein
  6. ^ http://www.yachatspresbyterian.org/webapp/GetPage?pid=211

References

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Ágata

Ágata


Ágata
Categoria Tipo de quartzo
Cor Branco, cinza, azul, laranja, verde, preto.
Fórmula química Silica, SiO2
Propriedades cristalográficas
Sistema cristalino Hexagonal
Hábito cristalino sílica criptocristalina
Propriedades óticas
Índice refrativo 1.530-1.540
Birrefringência até +0.004 (B-G)
Propriedades físicas
Peso específico 2.58-2.64
Densidade 2,6
Clivagem Não tem
Fratura Concoidal com bordas muito afinadas
Brilho Ceroso
Risca Branco
Ágata é uma subvariedade de Calcedônia, ou seja, é um tipo de quartzo. Caracteriza-se pela variedade de cores, geralmente dispostas em faixas paralelas.
De acordo com Teofrasto a ágata (achates) foi nomeada do rio Achates, agora o Drillo, na Sicília, onde o mineral foi primeiramente encontrado.

Índice

Formação e características

A maioria das ágatas ocorre como nódulos em rochas eruptivas, ou antigas lavas, onde preenchem as cavidades produzidas originalmente pela desagregação do vapor na massa derretida, e então preenchido, completamente ou parcialmente, pela matéria silicosa depositada em camadas regulares em cima das paredes. Tais ágatas, quando cortadas transversalmente, exibem uma sucessão de linhas paralelas, frequentemente de extrema tenuidade, dando uma aparência unida à seção, e por isso tais minerais são conhecidas como ágata unida e ágata listrada.
Na formação de uma ágata ordinária, é provável que as águas que contêm sílica dissolvida – derivada, talvez, da decomposição de alguns dos silicatos presentes na própria lava – infiltraram-se através da rocha, depositando um revestimento silicioso no interior das vesículas produzidas por vapor. As variações no caráter da solução, ou nas condições de deposição, podem causar variações correspondentes nas camadas sucessivas, de modo que as faixas de calcedónia frequentemente alternam com camadas de quartzo cristalino. Várias vesículas de vapor podem unir-se enquanto a rocha for viscosa, e assim dar forma a uma cavidade grande que possa se transformar em receptáculo de uma ágata de tamanho excepcional; assim um geode brasileiro, revestido de ametista, pesando 35 toneladas, foi exibido na Exposição de Dusseldorf de 1902.
O primeiro depósito na parede de uma cavidade, dando forma à "pele" da ágata, é geralmente uma substância mineral esverdeada escura, como celadonite, delessite ou "terra verde," os quais são ricos em ferro, derivado provavelmente da decomposição de augite na rocha-mãe. Este silicato verde pode dar origem, por alteração, a um óxido marrom do ferro (limonite), produzindo uma aparência oxidada na parte externa do nódulo de ágata. A superfície exterior de uma ágata, liberta da sua matriz, é frequentemente áspera, aparentemente na conseqüência da remoção do revestimento original. A primeira camada depositada sobre a parede da cavidade é por alguns chamada de "iniciador," e em cima desta base os minerais zeolíticos podem ser depositados.
Muitas ágatas são ocas, uma vez que a deposição não prosseguiu pelo tempo suficiente para encher a cavidade, e nesses casos o último depósito consiste geralmente de quartzo, frequentemente ametista, tendo os ápices dos cristais dirigidos para o espaço livre, formando uma cavidade, uma drusa ou um geodo revestido por cristais.

Variedades de ágata

Uma ágata mexicana, apresentando um único olho, recebeu o nome de "ciclope." Matéria inclusa de uma cor verde, como fragmentos de "terra verde," embutida na calcedônia e disposta em filamentos e outras formas sugestivas de crescimento vegetal, dá origem à ágata do musgo.
Com a desintegração da matriz em que as ágatas estão encaixadas, estas são libertadas, e, sendo por sua natureza siliciosa extremamente resistentes à ação do ar e da água, permanecem como nódulos no solo e no cascalho, ou tornam-se roladas como seixos nos córregos.
As ágatas dendríticas apresentam bonitos padrões em forma de feto formados devido à presença de íons de ferro e manganês. Outros tipos de materiais inclusos depositados durante a formação de ágatas incluem crescimentos sageníticos (cristais radiais) bem como pedaços de detritos retidos (como areia, cinza, ou lama). Ocasionalmente as ágatas preenchem vazios produzidos pela decomposição de matéria vegetal, como um ramo de árvore ou raíz designando-se por ágata de molde.
A ágata Turritella é formada a partir de fósseis de conchas de Turritella silicificados numa base de Calcedónia. A Turritela é um gastrópode marinho com conchas alongadas, em forma de espiral com muitas volutas.
De igual modo, os corais, madeira petrificada e outros restos orgânicos ou rochas porosoas podem ser "agatizados". O coral "agatizado" é muitas vezes denominado ágata ou pedra de Petoskey.
Determinadas pedras, quando examinadas em seções finas pela luz transmitida, apresentam um espectro de difracção, devido à extrema delicadeza das faixas sucessivas, sendo então denominadas ágatas do arco-íris.
Outras formas de ágata incluem a ágata carneliana (com tons avermelhados), ágata do Botsuana, ágata laço azul, ágata pluma, ágata tubo (com canais de fluzo visíveis), ágata fortificação (que exibem pouca ou nenhuma estruturação laminar), ágata do fogo (que parece brilhar internamente como uma opala).

A ágata e as crenças

Segundo o Islão, as ágatas são pedras muito preciosas. Segundo a tradição, acredita-se que o portador de um anel de ágata, por exemplo, está protegido contra vários infortúnios e gozará de longa vida, entre outros benefícios. Em outras tradições crê-se que a ágata cura as picadas do escorpião e as mordidas de serpente, acalma a mente, previne doenças e contágios, para a trovoada, promove a eloquência, assegura os favores dos poderosos e traz a vitória sobre os inimigos. Os magi Persas também apreciavam os anéis de ágata no seu trabalho e nas suas crenças.