Search results for "MINERALOGY"
showing 10 items of 1516 documents
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…
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…
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…
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…
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…
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…
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…
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…
Modelling carbon isotopes of carbonates in cave drip water
2011
Abstract C isotopes in cave drip water are affected by both the C isotope composition of soil air and host rock carbonate. Furthermore, the C isotope composition of cave drip water strongly depends on the calcite dissolution system, i.e., open, closed and intermediate conditions. Here, we present a calcite dissolution model, which calculates the 14C activity and δ13C value of the dissolved inorganic carbon of the drip water. The model is based on the chemical equations describing calcite dissolution ( H 2 O + CaCO 3 + CO 2 ⇔ Ca 2 + + 2HCO 3 - ). The most important improvement, relative to previous models, is the combination of the open and closed system conditions in order to simulate the C…
Pore scale modelling of calcite cement dissolution in a reservoir sandstone matrix
2019
E3S Web of Conferences 98, 05010 (1-5) (2019). doi:10.1051/e3sconf/20199805010