OXYGEN ISOTOPE FRACTIONATION IN SYNTHETIC MAGNESIAN CALCITE

dc.contributor.authorJimenez-Lopez C.
dc.contributor.authorRomanek C.S.
dc.contributor.authorHuertas F.J.
dc.contributor.authorOhmoto H.
dc.contributor.authorCaballero E.
dc.date.accessioned2022-03-21T07:44:13Z
dc.date.available2022-03-21T07:44:13Z
dc.date.issued2004
dc.description.abstractMg-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.identifierhttps://www.elibrary.ru/item.asp?id=12090497
dc.identifier.citationGeochimica et Cosmochimica Acta, 2004, 68, 16, 3367-3377
dc.identifier.issn0016-7037
dc.identifier.urihttps://repository.geologyscience.ru/handle/123456789/36485
dc.subjectcalcite
dc.titleOXYGEN ISOTOPE FRACTIONATION IN SYNTHETIC MAGNESIAN CALCITE
dc.typeСтатья

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