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showing 10 items of 4660 documents

Climatic dependence of stable carbon and oxygen isotope signals recorded in speleothems: From soil water to speleothem calcite

2011

Abstract Understanding the relationship between stable isotope signals recorded in speleothems (δ 13 C and δ 18 O) and the isotopic composition of the carbonate species in the soil water is of great importance for their interpretation in terms of past climate variability. Here the evolution of the carbon isotope composition of soil water on its way down to the cave during dissolution of limestone is studied for both closed and open-closed conditions with respect to CO 2 . The water entering the cave flows as a thin film towards the drip site. CO 2 degasses from this film within approx. 10 s by molecular diffusion. Subsequently, chemical and isotopic equilibrium is established on a time scal…

CalciteHydrologygeographygeography.geographical_feature_categoryStable isotope ratioMineralogySpeleothemOxygen isotope ratio cycleIsotopes of oxygenchemistry.chemical_compoundIsotope fractionationchemistryGeochemistry and PetrologySoil waterCarbonateGeologyGeochimica et Cosmochimica Acta
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Modelling the δ18O value of cave drip water and speleothem calcite

2010

Abstract Stable isotope signals recorded in speleothems have provided important insights about past climate variability in recent years. Quantitative reconstruction of mean annual temperature and the amount of precipitation, however, remains difficult because the stable isotope signals are influenced by various processes. Here we present a drip water model, which shows how these climate parameters affect the oxygen isotope signal of cave drip water. In the model the dependence of the δ 18 O value of drip water on mean annual temperature is established by correlation to the amount of winter precipitation and winter temperature. Application of the model to two caves in western Germany reveals…

CalciteHydrologygeographygeography.geographical_feature_categoryStable isotope ratioδ18OSpeleothemStalagmiteOxygen isotope ratio cycleAtmospheric sciencesIsotopes of oxygenchemistry.chemical_compoundGeophysicsIsotope fractionationchemistrySpace and Planetary ScienceGeochemistry and PetrologyEarth and Planetary Sciences (miscellaneous)GeologyEarth and Planetary Science Letters
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Detection and origin of different types of annual laminae in recent stalagmites from Zoolithencave, southern Germany: Evaluation of the potential for…

2016

Abstract. An arrangement of three stalagmites from Zoolithencave (southern Germany) was analysed for different types of annual laminae using both microscopic and geochemical methods. The speleothems show visible laminae (consisting of a clear and a brownish, pigmented layer pair) as well as fluorescent and elemental laminae. The age of the speleothems was constrained to 1800 to 1970 AD by 14C-dating of a charcoal piece below the speleothems, detection of the 14C bomb peak, as well as counting of annual laminae. Dating by the 230Th/U-method was impossible due to detrital contamination. On the annual time-scale, the variability of Mg, Ba, and Sr is controlled by Prior Calcite Precipitation (P…

CalciteWet seasongeographygeography.geographical_feature_category010504 meteorology & atmospheric sciencesStalagmite010502 geochemistry & geophysics01 natural scienceschemistry.chemical_compoundOceanographychemistryvisual_artvisual_art.visual_art_mediumPhysical geographyCharcoalGeology0105 earth and related environmental sciences
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Chemical evolution of dissolved inorganic carbon species flowing in thin water films and its implications for (rapid) degassing of CO2 during speleot…

2013

Abstract Rapid degassing of CO2 from a thin film of drip water on the surface of stalagmites is often considered to have a large effect on both speleothem growth and stable isotope values and is offered as an explanation for higher δ13C and δ18O values than expected under conditions of stable isotope equilibrium. However, the time constant for degassing of CO2 from the solution only depends on film thickness and the coefficient of molecular diffusion for CO2. Thus, for thin films, the time for degassing of CO2 is much shorter than the time for subsequent equilibration of the dissolved carbon species and precipitation of CaCO3. In this context, degassing of CO2 is always fast. Here we presen…

CalcitegeographyMolecular diffusiongeography.geographical_feature_categoryStable isotope ratioPrecipitation (chemistry)Analytical chemistrySpeleothemMineralogychemistry.chemical_elementContext (language use)chemistry.chemical_compoundchemistryGeochemistry and PetrologyDissolved organic carbonCarbonGeochimica et Cosmochimica Acta
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Lithium isotopes and partition coefficients in inorganic carbonates: Proxy calibration for weathering reconstruction

2021

We report Li measurements from cave-analogue carbonate-precipitation experiments in order to: i) assess the expected isotope fractionation factors applicable to speleothem growth, and ii) contribute to the wider understanding of lithium incorporation in carbonates. The experimental setup closely mimics natural processes (e.g. precipitation driven by CO2 degassing, low ionic strength solution, thin solution film) but within a laboratory setting that allows for controlled growth conditions (temperature, pCO2, drip rate, carbonate saturation index and the composition of the initial solution). For the main batch of calcite growth experiments our average 1000lnαcalcite-solution is -8.5&plu…

Calcitegeographygeography.geographical_feature_category010504 meteorology & atmospheric sciencesAragoniteIsotopes of lithiumAnalytical chemistrySpeleothemengineering.material010502 geochemistry & geophysics01 natural scienceschemistry.chemical_compoundIsotope fractionationchemistryGeochemistry and PetrologyengineeringCarbonateGrowth rateSaturation (chemistry)0105 earth and related environmental sciencesGeochimica et Cosmochimica Acta
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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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