1982
DOI: 10.1016/0009-2541(82)90053-5
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Kinetically controlled variations of major components and carbon and oxygen isotopes in a calcite-precipitating spring

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Cited by 159 publications
(88 citation statements)
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“…Geochemical modelling (Amiotte-Suchet and Probst, 1995;Gaillardet et al, 1997;Probst et al, 1997) and geochemical tracers (Négrel et al, 1993;Probst et al, 1994;Gaillardet et al, 1999;Mortatti and Probst, 2003) have been used to distinguish DIC originating from atmospheric/soil CO 2 and from carbonate dissolution. Nevertheless, each DIC source has a different υ 13 C isotopic signature ( 26 to 9‰ for soil organic matter according to whether C 3 or C 4 plants (Mariotti, 1991), 8 to 6‰ for atmospheric CO 2 (Cerling et al, 1991) and around 0‰ for carbonate rocks (Keith and Weber, 1964)), but few studies have been devoted to the use of carbon isotopes to trace the different DIC sources, to follow the riverine DIC transport into the ocean and to assess the carbon transformation in the river itself (Hitchon and Krouse, 1972;Dandurand et al, 1982;Kendall et al, 1992Kendall et al, , 1995Pawellek and Veizer, 1994;Cameron et al, 1995;Flintrop et al, 1996;Taylor and Fox, 1996;Yang et al, 1996;Amiotte-Suchet et al, 1999;Aucour et al, 1999;Barth and Veizer, 1999;Telmer and Veizer, 1999).…”
Section: Introductionmentioning
confidence: 99%
“…Geochemical modelling (Amiotte-Suchet and Probst, 1995;Gaillardet et al, 1997;Probst et al, 1997) and geochemical tracers (Négrel et al, 1993;Probst et al, 1994;Gaillardet et al, 1999;Mortatti and Probst, 2003) have been used to distinguish DIC originating from atmospheric/soil CO 2 and from carbonate dissolution. Nevertheless, each DIC source has a different υ 13 C isotopic signature ( 26 to 9‰ for soil organic matter according to whether C 3 or C 4 plants (Mariotti, 1991), 8 to 6‰ for atmospheric CO 2 (Cerling et al, 1991) and around 0‰ for carbonate rocks (Keith and Weber, 1964)), but few studies have been devoted to the use of carbon isotopes to trace the different DIC sources, to follow the riverine DIC transport into the ocean and to assess the carbon transformation in the river itself (Hitchon and Krouse, 1972;Dandurand et al, 1982;Kendall et al, 1992Kendall et al, , 1995Pawellek and Veizer, 1994;Cameron et al, 1995;Flintrop et al, 1996;Taylor and Fox, 1996;Yang et al, 1996;Amiotte-Suchet et al, 1999;Aucour et al, 1999;Barth and Veizer, 1999;Telmer and Veizer, 1999).…”
Section: Introductionmentioning
confidence: 99%
“…Radiocarbon studies of ground water have resulted in the formulation of different models which estimate initial 14C activity of HC03-ions dissolved in water (Pearson, 1965;Vogel, 1970;Mook, 1976Mook, , 1980Eichinger, 1983). However, physi-cochemical processes involved in precipitation of tufa are complex, and numerous environmental factors may influence them (Friedman, 1970;Usdowski, Hoefs & Menschel, 1979;Dandurand et al, 1982;Michaelis, Usdowski & Menschel, 1985; Thorpe, Otlet & Sweeting, 1980;Szulc, 1984). Direct application of such models in 14C dating of tufa has led to unsatisfactory results (Thorpe et al, 1981;Krajcar et al, 1985).…”
Section: Introductionmentioning
confidence: 99%
“…The general nature of the diurnal trends observed at Davys Creek is similar to that documented at other sites around the world (Barnes, 1965;Dandurand et al, 1982;Spiro and Pentecost, 1991;Pentecost, 1994): at-a-station minima in dissolved ions (measured as SC or dissolved CaCO 3 ) usually occur in the mid-afternoon when water temperature reaches its maximum and P CO 2 is closest to atmospheric levels, whereas maximum ion concentrations between sunrise and mid-morning coincide with minimum water temperatures and P CO 2 peaks.…”
Section: Controls On An Individual Diurnal Cyclementioning
confidence: 59%