Aragonite

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.

Occurrence

The aragonite was described by José Torrubia in 1754, as he indicated the existence of large quantities of "hexagonal" crystals, locally called "torrecillas", in a hill near the river Gallo, in Molina de Aragon. and named from types located in Molina de Aragón in the Province of Guadalajara in Castilla-La Mancha, Spain by Abraham Gottlob Werner in 1797, although he mistaked that Molina de Aragon was in Aragon. 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, the Ochtinská Aragonite Cave, is situated in Slovakia. Another cave of outstanding importance for its aragonite speleothems is Cave of El Soplao. Located within a former lead and zinc mining complex in Rionansa, Cantabria (Spain), it was discovered in 1908 and subsequently used as a transport gallery for mined ore until the closure of the mine in 1978. Since 2005, the cave has been open to the public as a tourist attraction.

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 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 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 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 a calcium chloride solution to a sodium carbonate solution at temperatures above 60 °C (140 °F) or in water-ethanol mixtures at ambient temperatures.