Search results for "calcite"

showing 10 items of 191 documents

Determination of aragonite trace element distribution coefficients from speleothem calcite–aragonite transitions.

2016

The processes that govern the incorporation of (trace) elements into speleothems can often be linked to environmental changes. Although element incorporation into speleothem calcite is now reasonably well understood, current knowledge regarding trace element variability in speleothem aragonite is very limited. Of particular interest is whether trace element distribution coefficients are above or below one in order to assess the extent to which prior aragonite precipitation has affected speleothem aragonite trace element records. This study uses nine calcite-to-aragonite transitions in seven speleothems from diverse environmental settings to derive the first quantitative estimates of the dis…

Calcitegeographygeography.geographical_feature_category010504 meteorology & atmospheric sciencesAragoniteTrace elementMineralogySpeleothemF700StalagmiteF800engineering.materialF600010502 geochemistry & geophysics01 natural sciencesF900chemistry.chemical_compoundchemistryGeochemistry and PetrologyengineeringGrowth rateNegative correlationGeology0105 earth and related environmental sciences
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Processes affecting the stable isotope composition of calcite during precipitation on the surface of stalagmites: Laboratory experiments investigatin…

2016

Abstract We present a theoretical derivation of the exchange time, τex, needed to establish isotopic equilibrium between atmospheric CO2 in a cave and HCO3− dissolved in a thin water film covering the surface of a speleothem. The result is τ ex = τ red ex · [ HCO 3 - ] K H · p CO 2 cave , where τ red ex depends on the depth, a, of the water film and on temperature. [ HCO 3 - ] is the concentration of bicarbonate, p CO 2 cave the partial pressure of CO2, and KH is Henry’s constant. To test the theory we prepared stagnant or flowing thin films of a NaHCO3 solution and exposed them at 20 °C to an CO2 containing atmosphere of p CO 2 500, 12,500, or 25,000 ppmV and defined isotope composition. T…

Calcitegeographygeography.geographical_feature_category010504 meteorology & atmospheric sciencesChemistryδ18OStable isotope ratioAnalytical chemistryMineralogySpeleothemStalagmitePartial pressure010502 geochemistry & geophysics01 natural sciencesAtmospherechemistry.chemical_compoundGeochemistry and PetrologyDissolved organic carbon0105 earth and related environmental sciencesGeochimica et Cosmochimica Acta
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Coarse-grained cryogenic aragonite as end-member of mineral formation in dolomite caves

2018

Abstract Cryogenic carbonate particles (single crystals and aggregates) have recently been recognized as important witnesses of permafrost dynamics, as they can be used to estimate the thickness and timing of development of permafrost. In this study, the petrography and geochemistry of coarse-grained cryogenic aragonite (CGCAr) identified in Zoolithen Cave in NE Bavaria, Germany, are described in detail for the first time. We provide a sequence of carbonate precipitation during freezing, where CGCAr mark the final crystallization phase in freezing water on ice. Our results support the notion that host rock composition, solution chemistry, and cave ventilation play an important role for arag…

Calcitegeographygeography.geographical_feature_category010504 meteorology & atmospheric sciencesStratigraphyAragoniteDolomiteGeochemistryGeologyengineering.material010502 geochemistry & geophysicsPermafrost01 natural sciencesPetrographychemistry.chemical_compoundCavechemistryIsotopes of carbonengineeringCarbonateGeology0105 earth and related environmental sciencesSedimentary Geology
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Constraining speleothem oxygen isotope disequilibrium driven by rapid CO2 degassing and calcite precipitation: Insights from monitoring and modeling

2020

Abstract Oxygen isotopes are the most commonly applied speleothem proxy for reconstructing Quaternary changes in precipitation and/or temperature. These interpretations are either limited to qualitative wetting and drying trends or rely on theoretical, experimental and/or empirical equilibrium isotope fractionation factors for more quantitative constraints. These various fractionation factors have similar temperature sensitivities, but their absolute values differ, and cave calcite does not appear to generally precipitate in isotopic equilibrium with its drip water. Rapid CO2 degassing paired with calcite precipitation, both occurring under disequilibrium conditions, are a set of mechanisms…

Calcitegeographygeography.geographical_feature_category010504 meteorology & atmospheric sciencesδ18OSpeleothemMineralogyStalagmite010502 geochemistry & geophysics01 natural sciencesIsotopes of oxygenchemistry.chemical_compoundIsotope fractionationchemistryCaveGeochemistry and PetrologyPaleoclimatologyEnvironmental science0105 earth and related environmental sciencesGeochimica et Cosmochimica Acta
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The geological CO2degassing history of a long-lived caldera

2015

The majority of the ~100 Holocene calderas on Earth host vigorously active hydrothermal systems, the heat and volatile budgets of which are sustained by degassing of deeply stored magma. Calderas may thus contribute a nontrivial, although poorly quantified, fraction of the global budget of magmatic volatiles such as CO2. Here we use original isotopic a d petrological results from Campi Flegrei volcano, Italy, to propose that hydrothermal calcites are natural mineral archives for the magmatic CO2 that reacted with reservoir rocks during the geological history of a caldera. We show that Campi Flegrei calcites, identified in core samples extracted from 3-km-deep geothermal wells, formed at iso…

Calcitegeographygeography.geographical_feature_categoryEarth scienceGeochemistryGeologyHydrothermal circulationFumarolechemistry.chemical_compoundVolcanochemistryMagmaCalderaGeothermal gradientHoloceneGeologyGeology
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Hydrogeochemistry and fractionation pathways of Mg isotopes in a continental weathering system: Lessons from field experiments

2012

Abstract The potential of magnesium isotope records from cave carbonate archives (speleothems) has been documented but remains underexplored. This is due to the limited knowledge regarding the complex suite of physico-chemical and biological disequilibrium fractionation processes affecting meteoric fluids in the soil zone, the carbonate hostrock and calcite precipitation in the cave. This study presents δ 26  Mg data from a monitored cave in Germany (Bunker Cave) including rain water (δ 26  Mg: − 0.70 ± 0.14‰), soil water (δ 26  Mg: − 0.51 ± 0.10‰) and drip waters (δ 26  Mg: − 1.65 ± 0.08‰) sampled between November 2009 and May 2011. Field precipitation experiments, i.e., calcite precipitat…

Calcitegeographygeography.geographical_feature_categoryGeochemistrySpeleothemGeologyWeatheringchemistry.chemical_compoundchemistryCaveGeochemistry and PetrologySoil waterCarbonatePrecipitationClay mineralsGeologyChemical Geology
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Textural features and isotope geochemistry of the Scillato travertine (north-central Sicily): genetic implications.

2015

The travertine deposit, outcropping near the Scillato town (north-central Sicily), was originated by precipitation of calcium carbonate from the Scillato springs, documented as bicarbonate-enriched waters due to dissolution of the Madonie mountains carbonate rocks. This deposit is today well represented by the Travertine Cave, essentially constituted by stalactites and stalagmites in which travertine typically appears laminated with alternation of light and dark laminae. Mineralogical analysis have revealed the almost exclusive presence of calcite and observation under the polarized-light microscope showed different textural features, like presence of debris and porous portions, micritic po…

Calcitegeographygeography.geographical_feature_categoryMineralogyGeologyStalagmiteSedimentary depositional environmentchemistry.chemical_compoundCalcium carbonatechemistryCaveTufaIsotope geochemistryGeneral Earth and Planetary SciencesCarbonate rockwaterfall tufa speleothems stable carbon and oxygen isotopes microbial activityGeology
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Geochemistry and mineralogy of travertine deposits of the SW flank of Mt. Etna (Italy): Relationships with past volcanic and degassing activity

2007

Abstract Travertine deposits outcropping in the lower SW flank of Mt. Etna were studied for their mapping, as well as for their chemical, mineralogical and isotopic compositions. These deposits are dated to about 24 to 5 ka in the Adrano area, located at the western limit of the study area. In this area travertines show high Mg contents and are composed mostly of dolomite, thus apparently ruling out any primary deposition in favour of a diagenetic origin. Travertines outcropping near Paterno, in the east part of the study area, should be younger than 18 ka. Those located to the SSW of Paterno (Paterno–Diga) show high Sr contents and aragonite as dominant mineralogical phase, thus suggesting…

Calcitegeographygeography.geographical_feature_categoryOutcropAragoniteDolomiteGeochemistryMineralogyengineering.materialDiagenesischemistry.chemical_compoundGeophysicsVolcanochemistryGeochemistry and PetrologyengineeringCarbonate rockSedimentary rockGeologyJournal of Volcanology and Geothermal Research
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Disequilibrium carbon and oxygen isotope fractionation in recent cave calcite: Comparison of cave precipitates and model data

2013

Abstract Speleothem proxy data provide important information in continental palaeo-climate research due to their precise chronology and wide geographic distribution. Despite a continuously growing number of field and numerical studies designed to study stable isotope fractionation effects, many aspects remain a matter of debate. Here, carbon and oxygen isotope ratios from cave drip water and calcite precipitates sampled on watch glasses in the Bunker Cave (Western Germany) are compared with the values expected for isotopic equilibrium. Furthermore, the field data are compared with the results of a numerical model simulating stalagmite growth and stable isotope ratios. Two drip sites with di…

Calcitegeographygeography.geographical_feature_categoryStable isotope ratioδ18OSpeleothemMineralogyStalagmiteIsotopes of oxygenchemistry.chemical_compoundchemistryCaveGeochemistry and PetrologyWatch glassGeologyGeochimica et Cosmochimica Acta
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Are oxygen isotope fractionation factors between calcite and water derived from speleothems systematically biased due to prior calcite precipitation …

2021

Abstract The equilibrium oxygen isotope fractionation factor between calcite and water (18αcalcite/H2O) is an important quantity in stable isotope geochemistry and allows in principle to infer temperature variations from carbonate δ18O if carbonate formation occurred in thermodynamic equilibrium. For this reason, many studies intended to determine the value of the oxygen isotope fractionation factor between calcite and water (18αcalcite/H2O) for a wide range of temperatures using modern cave calcite and the corresponding cave drip water or ancient speleothem carbonate and fluid inclusion samples. However, the picture that emerges from all of these studies indicates that speleothem calcite i…

Calcitegeographygeography.geographical_feature_categoryStalactite010504 meteorology & atmospheric sciencesChemistryFOS: Physical sciencesSpeleothemMineralogyStalagmite010502 geochemistry & geophysics01 natural sciencesIsotopes of oxygenGeophysics (physics.geo-ph)Physics - Geophysicschemistry.chemical_compoundCaveGeochemistry and PetrologyIsotope geochemistryCarbonate0105 earth and related environmental sciences
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