2004
DOI: 10.1016/j.chemgeo.2004.01.012
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Cryogenic cave calcite from several Central European caves: age, carbon and oxygen isotopes and a genetic model

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Cited by 59 publications
(38 citation statements)
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“…It is therefore appears highly unlikely that hundreds of years separated the two calcite generations, but rather a much shorter time span, probably a few years at most. These isotopic observations add support to the model of CCC coarse formation suggesting that these crystals originate in small pools of meltwater carved in cave ice (Žák et al, 2004;Richter and Riechelmann, 2008) and experiencing very slow refreezing under closed-system conditions (Kluge et al, 2014). Our data show that there were several such (Nicolussi et al, 2005), advances of the east-Alpine Gepatsch Glacier beyond the extent of the 1940 AD glacier size (Nicolussi and Patzelt, 2001), a speleothembased record of the ice surface elevation of the Upper Grindelwald Glacier (Luetscher et al, 2011), 10 Be-dated evidence of a marked advance of Stein Glacier, Switzerland (Schimmelpfennig et al, 2014), and a semicontinuous glacier-length record of the Great Aletsch Glacier in the Western Alps (Holzhauser et al, 2005) for the last four millennia.…”
Section: Stable Isotopes and The Mode Of CCC Coarse Formationsupporting
confidence: 50%
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“…It is therefore appears highly unlikely that hundreds of years separated the two calcite generations, but rather a much shorter time span, probably a few years at most. These isotopic observations add support to the model of CCC coarse formation suggesting that these crystals originate in small pools of meltwater carved in cave ice (Žák et al, 2004;Richter and Riechelmann, 2008) and experiencing very slow refreezing under closed-system conditions (Kluge et al, 2014). Our data show that there were several such (Nicolussi et al, 2005), advances of the east-Alpine Gepatsch Glacier beyond the extent of the 1940 AD glacier size (Nicolussi and Patzelt, 2001), a speleothembased record of the ice surface elevation of the Upper Grindelwald Glacier (Luetscher et al, 2011), 10 Be-dated evidence of a marked advance of Stein Glacier, Switzerland (Schimmelpfennig et al, 2014), and a semicontinuous glacier-length record of the Great Aletsch Glacier in the Western Alps (Holzhauser et al, 2005) for the last four millennia.…”
Section: Stable Isotopes and The Mode Of CCC Coarse Formationsupporting
confidence: 50%
“…The latter data set comprises data from 11 stalagmites, including the COMNISPA2 stack (Fohlmeister et al, 2013). (c) CCC coarse samples from MSK Cave in comparison to published CCC coarse (green) and CCC fine (light blue) data from non-Alpine caves in Romania, Slovakia, Poland, Czech Republic, Germany and Canada (data from Clark and Lauriol, 1992;Žák et al, 2004Richter et al, 2013;Orvošová et al, 2014). The dark blue array labeled ERW shows data of in situ CCC fine from Eisriesenwelt in the Austrian Alps (Spötl, 2008).…”
Section: Characteristics Of CCC Coarsementioning
confidence: 99%
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“…It has been suggested by Žák et al (2008) that fine-grained calcite powders formed during the rapid freezing of water, whereas a more-coarsed grain type formed during the slow freezing of water. Cryogenic cave calcite pearls (spherolites) are a specific type of speleothem currently only discovered in Central European caves (Žák et al, 2004;Richter & Niggemann, 2005).…”
Section: Introductionmentioning
confidence: 99%
“…These δ 13 C CaCO3 values are lower than that expected from carbonates precipitated from dissolved inorganic carbon (DIC) in equilibrium with atmospheric CO 2 ; the δ 13 C CO2 at South Pole station ranges from À8.2 to À7.5‰ (Allison et al, 2003) which would yield a δ 13 C CaCO3 ranging from +3.0‰ (pH = 6.6) to +6.5‰ (pH > 9.0) under equilibrium condition (Bottinga, 1968). The formation of carbonates under equilibrium freezing of water with solely a dissolved atmospheric CO 2 source can be ruled out since the δ 13 C DIC would progressively increase during freezing under both open and closed conditions as a result of the removal of light CO 2 from the system during calcite precipitation (Socki et al, 2001;Zak et al, 2004Zak et al, , 2008. The formation of carbonates under kinetic freezing or evaporation conditions can also be ruled out given that the 13 C CO 2 -CaCO 3 fractionation factor is greater than under equilibrium conditions (kinetic freezing: ε 13 C CO 2 -CaCO 3 = 31.2 ±3.1‰ at 0°C; Clark & Lauriol, 1992; kinetic evaporation: ε 13 C CO 2 -CaCO 3 = 19.9 ± 7.8‰ at 22°C; Lacelle et al, 2007).…”
Section: Discussionmentioning
confidence: 99%