A calcite sea is a sea in which low-magnesium calcite is the primary inorganic marine calcium carbonate precipitate. An aragonite sea is the alternate seawater chemistry in which aragonite and high-magnesium calcite are the primary inorganic carbonate precipitates. The Early Paleozoic and the Middle to Late Mesozoic oceans were predominantly calcite seas, whereas the Middle Paleozoic through the Early Mesozoic and the Cenozoic (including today) are characterized by aragonite seas.
The most significant geological and biological effects of calcite sea conditions include rapid and widespread formation of carbonate hardgrounds, calcitic ooids, calcite cements, and the contemporaneous dissolution of aragonite shells in shallow warm seas. Hardgrounds were very common, for example, in the calcite seas of the Ordovician and Jurassic, but virtually absent from the aragonite seas of the Permian.
Fossils of invertebrate organisms found in calcite sea deposits are usually dominated by either thick calcite shells and skeletons, were infaunal and/or had thick periostraca, or had an inner shell of aragonite and an outer shell of calcite. This was apparently because aragonite dissolved quickly on the seafloor and had to be either avoided or protected as a biomineral.
Calcite seas were coincident with times of rapid seafloor spreading and global greenhouse climate conditions. Seafloor spreading centers cycle seawater through hydrothermal vents, reducing the ratio of magnesium to calcium in the seawater through metamorphism of calcium-rich minerals in basalt to magnesium-rich clays. This reduction in the Mg/Ca ratio favors the precipitation of calcite over aragonite. Increased seafloor spreading also means increased volcanism and elevated levels of carbon dioxide in the atmosphere and oceans. This may also have an effect on which polymorph of calcium carbonate is precipitated. Further, high calcium concentrations of seawater favor the burial of CaCO3, thereby removing alkalinity from the ocean, lowering seawater pH and reducing its acid/base buffering.
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This course builds on environmental chemistry and microbiology taken in previous courses. The emphasis is on quantification using the public domain package, PHREEQC, which is an excellent computation
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In hardwater lakes, calcite precipitation is an important yet poorly understood process in the lacustrine carbon cycle, in which catchment-derived alkalinity (Alk) is both transformed and translocated. While the physico-chemical conditions supporting the s ...
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One of the most conserved traits in the evolution of biomineralizing organisms is the taxon-specific selection of skeletal minerals. All modern scleractinian corals are thought to produce skeletons exclusively of the calcium-carbonate polymorph aragonite. ...
L’aragonite est un minéral composé de carbonate de calcium (avec des traces de Sr, Pb et Zn), c'est donc un polymorphe de la calcite et de la vatérite. Ses cristaux peuvent atteindre de long. L'aragonite a été décrite dès 1609 par Anselmus Boëtius de Boodt sous le nom de stillatitius lapis, mais sa description moderne de référence est celle d'Abraham Gottlob Werner en 1797. Le mot aragonite dérive de son topotype, proche de Molina de Aragón, en Espagne. Molina de Aragón, dans la province de Guadalajara (région de Castille-La Manche, Espagne).
La calcite est un minéral, pouvant être d'origine biochimique (biominéralisation), composé de carbonate naturel de calcium de formule CaCO3, avec des traces de certains métaux de transition, certains métaux alcalino-terreux et deux métaux post-transitionnels. L'abondance des cations autres que le calcium explique la richesse des variétés décrites pour ce minéral. Polymorphe de l’aragonite et de la vatérite, isostructurale avec la nitratine et l'otavite, la calcite forme une série continue avec la rhodochrosite.