OXYGEN ISOTOPE FRACTIONATION IN SYNTHETIC MAGNESIAN CALCITE

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dc.contributor.author Jimenez-Lopez C.
dc.contributor.author Romanek C.S.
dc.contributor.author Huertas F.J.
dc.contributor.author Ohmoto H.
dc.contributor.author Caballero E.
dc.date.accessioned 2022-03-21T07:44:13Z
dc.date.available 2022-03-21T07:44:13Z
dc.date.issued 2004
dc.identifier https://www.elibrary.ru/item.asp?id=12090497
dc.identifier.citation Geochimica et Cosmochimica Acta, 2004, 68, 16, 3367-3377
dc.identifier.issn 0016-7037
dc.identifier.uri https://repository.geologyscience.ru/handle/123456789/36485
dc.description.abstract Mg-bearing calcite was precipitated at 25°C in closed system free-drift experiments from solutions containing NaHCO3, CaCl2 and MgCl2. The chemical and isotope composition of the solution and precipitate were investigated during time course experiments of 24-h duration. Monohydrocalcite and calcite precipitated early in the experiments (<8 h), while Mg-calcite was the predominant precipitate (>95%) thereafter. Solid collected at the end of the experiments displayed compositional zoning from pure calcite in crystal cores to up to 23 mol% MgCO3 in the rims. Smaller excursions in Mg were superimposed on this chemical record, which is characteristic of oscillatory zoning observed in synthetic and natural solid-solution carbonates of differing solubility. Magnesium also altered the predominant morphology of crystals over time from the {104} to {100} and {110} growth forms.
dc.subject calcite
dc.title OXYGEN ISOTOPE FRACTIONATION IN SYNTHETIC MAGNESIAN CALCITE
dc.type Статья


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