Search results for "CALCITE"

showing 10 items of 191 documents

Clumped isotope thermometry of carbonate-bearing apatite: Revised sample pre-treatment, acid digestion, and temperature calibration

2016

Abstract It has recently been shown that the clumped isotopic composition (Δ47) of carbonate-bearing hydroxyapatite (CHAP) from teeth and bones reveals important information about the body temperature of vertebrates (Eagle et al., 2010, 2011). In this study we reinvestigate the temperature dependence of Δ47 in CHAP, extending the temperature range from 2 to 59 °C. In addition, the effects of chemical pre-treatment of CHAP on its bulk and clumped isotopic composition are studied. CHAP is best reacted with phosphoric acid at 90 to 110 °C minimizing the potential of evolved CO2 or reaction intermediates to re-equilibrate with traces of water in the acid environment. Reaction at 110 °C ensures …

CalciteEnamel paintAragonite010401 analytical chemistryAnalytical chemistryMineralogyGeologyAtmospheric temperature rangeengineering.material010502 geochemistry & geophysicsTooth enamel01 natural sciencesApatite0104 chemical scienceschemistry.chemical_compoundmedicine.anatomical_structurechemistryGeochemistry and Petrologyvisual_artmedicinevisual_art.visual_art_mediumengineeringCarbonatePhosphoric acid0105 earth and related environmental sciencesChemical Geology
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Transition from marine to hypersaline conditions in the Messinian Tripoli Formation from the marginal areas of the central Sicilian Basin

2001

Abstract Three sections of the early Messinian Tripoli Formation from the northern and southern margins of the central Sicilian Basin (Serra Pirciata, Torrente Vaccarizzo, and Marianopoli) have been studied with the aim to reconstruct the sedimentary and environmental changes which occurred during the transition between marine conditions and the evaporitic events of the Salinity Crisis recorded in the overlying Calcare di Base Formation. A detailed biostratigraphic and cyclostratigraphic study provided the opportunity of cycle-by-cycle correlations between the marginal sections and the reference section of Falconara. The main paleoenvironmental changes are recorded by: (1) the evolution of …

CalciteEvaporiteStratigraphyAragoniteDolomiteGeologyAuthigenicengineering.materialPaleontologychemistry.chemical_compoundWater columnchemistryengineeringCarbonateSedimentary rockGeologySedimentary Geology
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THE REDISTRIBUTION OF RARE-EARTH ELEMENTS IN SECONDARY MINERALS OF HYDROTHERMAL VEINS, SCHWARZWALD, SOUTHWESTERN GERMANY

2011

Minerals of the rare-earth elements (REE) occur as supergene phases in the Schwarzwald ore district, southwestern Germany. They form by alteration of hydrothermal fluorite – barite – quartz – carbonate veins with various associations, including Cu– Pb, Pb–Zn and Co–Bi–Ag–U assemblages in sandstones, gneisses and granites. The REE minerals, including mixite-group minerals ([REE,Bi,Ca,Pb]Cu 6 (AsO 4 ,AsO 3 OH) 3 OH 6 •3H 2 O), rhabdophane and churchite (REEPO 4 •H 2 O and REEPO 4 •2H 2 O), chukhrovite (Ca 3 REEAl 2 SO 4 F 13 •10H 2 O) and bastnasite (REECO 3 F), were analyzed by electron microprobe and LA–ICP–MS. In addition, REE concentrations in secondary fluorite, calcite and Mn oxides cog…

CalciteGeochemistryMineralogyFluoriteHydrothermal circulationBastnäsitechemistry.chemical_compoundUraninitechemistryGeochemistry and PetrologyCarbonateQuartzGeologyGneissThe Canadian Mineralogist
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A biogeochemical model for chalk alteration by fungi in semiarid environments

1996

Fungal filaments are the most abundant organic features in weathered profiles developed on chalky limestone ("platy calcrete"). Their activity affects the mineral dynamics of the pore/carbonate microsystem. A theoretical biogeochemical model is proposed to describe the Ca-oxalate-carbonate cycle related to fungal activity in dry environments.

CalciteGeochemistryMineralogyGeochemical cyclechemistry.chemical_compoundCalcium carbonatechemistryEnvironmental ChemistryCarbonate rockCarbonateSedimentary rockEcosystemGeologyEarth-Surface ProcessesWater Science and TechnologyBiomineralizationBiogeochemistry
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Reconstruction of drip-water δ<sup>18</sup>O based on calcite oxygen and clumped isotopes of speleothems from Bunker Cave…

2013

Abstract. The geochemical signature of many speleothems used for reconstruction of past continental climates is affected by kinetic isotope fractionation. This limits quantitative paleoclimate reconstruction and, in cases where the kinetic fractionation varies with time, also affects relative paleoclimate interpretations. In carbonate archive research, clumped isotope thermometry is typically used as proxy for absolute temperatures. In the case of speleothems, however, clumped isotopes provide a sensitive indicator for disequilibrium effects. The extent of kinetic fractionation co-varies in Δ47 and δ18O so that it can be used to account for disequilibrium in δ18O and to extract the past dri…

CalciteGlobal and Planetary ChangegeographyEemiangeography.geographical_feature_category010504 meteorology & atmospheric sciencesδ18OStratigraphyDisequilibriumGeochemistryHolocene climatic optimumPaleontologyStalagmite010502 geochemistry & geophysics01 natural scienceschemistry.chemical_compoundPaleontologyIsotope fractionationchemistry13. Climate actionKinetic fractionationmedicinemedicine.symptomGeology0105 earth and related environmental sciences
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Bulk carbonate isotope stratigraphy from CRP-3 core (Victoria Land Basin, Antarctica): evidence for Eocene–Oligocene palaeoclimatic evolution

2005

Bulk carbonate isotope compositions and carbonate petrography from upper Eocene and lower Oligocene siliciclastic sediments of the CRP-3 sediment core (Victoria Land Basin, Antarctica) have been investigated with the aim of contributing to reconstruction of the Antarctic Cenozoic palaeoclimate. Most of the carbonate is calcite cement occurring as patches, nodules and horizons and consisting of equant and/or drusy sparry calcite, pervasive blocky calcite and rare poikilotopic calcite spar. 18O-depleted values (from −17 to −8 δ‰) of the CRP-3 carbonates suggest that the precipitating fluids were a mixing between marine and meteoric waters from melting glaciers. The δ18O record exhibits a numb…

CalciteGlobal and Planetary Changeδ18OOceanographyPetrographychemistry.chemical_compoundPaleontologyEocene/Oligocene Antarctica Stable isotopes Carbonate diagenesis PalaeoclimatologychemistryStratigraphyCarbonateSiliciclasticGlobal coolingCenozoicGeologyGlobal and Planetary Change
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Reactions and textures in grossular–wollastonite–scapolite calc–silicate granulites from Maligawila, Sri Lanka: evidence for high-temperature isobari…

2001

Grossular–wollastonite–scapolite calc–silicate granulites from Maligawila in the Buttala klippe, which form part of the overthrusted rocks of the Highland Complex of Sri Lanka, preserve a number of spectacular coronas and replacement textures that could be effectively used to infer their P–T–fluid history. These textures include coronas of garnet, garnet–quartz, and garnet–quartz–calcite at the grain boundaries of wollastonite, scapolite, and calcite as well as calcite–plagioclase and calcite– quartz symplectites or finer grains after scapolite and wollastonite respectively. Other textures include a double rind of coronal scapolite and coronal garnet between matrix garnet and calcite. The r…

CalciteGrossularMetamorphic rockGeochemistryScapoliteMineralogyMetamorphismGeologyengineering.materialGranuliteWollastonitechemistry.chemical_compoundchemistryGeochemistry and Petrologyvisual_artengineeringvisual_art.visual_art_mediumMetasomatismGeologyLithos
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Structure-Dependent Dissolution and Restructuring of Calcite Surfaces by Organophosphonates

2017

Organophosphonates are well-known to strongly interact with the surfaces of various minerals, such as brucite, gypsum, and barite. In this work, we study the influence of six systematically varied organophosphonate molecules (tetraphosphonates and diphosphonates) on the dissolution process of the (10.4) surface of calcite. In order to pursue a systematic study, we have selected organophosphonates that exhibit similar structural features, but also systematic architectural differences. The effect of this class of additives on the dissolution process of the calcite (10.4) surface is evaluated using in situ dynamic atomic force microscopy. For all of the six organophosphonate derivatives, we ob…

CalciteGypsumAtomic force microscopyBruciteDiphosphonates02 engineering and technologyGeneral Chemistryengineering.material010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics53001 natural sciences0104 chemical scienceschemistry.chemical_compoundCrystallographychemistryChemical engineeringengineeringMoleculeGeneral Materials ScienceOrganophosphonates0210 nano-technologyDissolutionCrystal Growth & Design
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Reactivity of gypsum faces according to the relative humidity by scanning force microscopy

1997

Abstract This article reports the experimental observation of the stability of the different faces of calcium sulphate dihydrate (gypsum CaSO 4 .2H 2 O) according to the relative humidity. Scanning Force Microscopy experiments were carried out with a view to discerning the topography of the surfaces, the chemical compositional domains, and in an attempt to evaluate the friction and viscoelastic properties of the surface. Our results indicate that the (010) face of gypsum is hydrophilic and very reactive contrary to the less hydrophilic (120) and (101) faces which remain stable depending on the relative humidity. It is clear from our results that a precipitation like process can be induced b…

CalciteGypsumPrecipitation (chemistry)MuscoviteSurfaces and Interfacesengineering.materialCondensed Matter PhysicsSurfaces Coatings and Filmschemistry.chemical_compoundCrystallographychemistryMicroscopyMaterials ChemistryengineeringRelative humidityMicaWettingComposite materialSurface Science
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Multianalytical Approach to explain the darkening process of hematite pigment in paintings from ancient Pompeii after accelerated weathering experime…

2013

[EN] In this paper, recently excavated fresco painting fragments from the House of Marcus Lucretius (Pompeii) and not exposed to the atmosphere since the eruption of the Mount Vesuvius were subjected to a controlled SO2 atmosphere and high relative humidity. These experiments were conducted in order to simulate under accelerated conditions the possible deterioration of the hematite pigment and plaster. The mineralogical transformation of the polychromy and plaster was monitored using mainly Raman spectroscopy, a non-destructive technique, but also infrared spectroscopy (FT-IR) and scanning electron microscopy energy-dispersive X-ray spectroscopy (SEM-EDS). After different exposure cycles to…

CalciteGypsumScanning electron microscopeGeneral Chemical EngineeringGeneral EngineeringMineralogyInfrared spectroscopyta6132Weatheringengineering.materialHematiteAnalytical Chemistrychemistry.chemical_compoundPigmentchemistryvisual_artengineeringvisual_art.visual_art_mediumNuclear chemistryMagnetite
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