Chemical and stable isotope composition of recent hot-water travertines and associated thermal waters, from Egerszalók, Hungary: Depositional facies and non-equilibrium fractionation

Sándor Kele, A. Demény, Zoltán Siklósy, Tibor Németh, Mária Tóth, Magdolna B. Kovács

Research output: Contribution to journalArticle

75 Citations (Scopus)

Abstract

Combined petrographical, mineralogical, geochemical and stable isotope analyses were conducted on an actively forming Egerszalók Travertine mound to determine the factors that govern carbonate precipitation and thus influence the use of travertines in paleoclimate reconstruction. Stable isotope analyses of oxygen, carbon and hydrogen demonstrate both biological and abiological factors to control travertine deposition. Processes of morphology-related outgassing had major effects upon isotopic composition. Continuous CO2 degassing and temperature change of the thermal water between the spring orifice and distal parts of the system, caused stable carbon and oxygen isotope compositions of the precipitating travertines to increase (from + 2.7 to + 4.3‰ relative to V-PDB and from + 10.5 to + 14.7‰ relative to V-SMOW, respectively). The travertines at the spring orifice (T ∼ 67 °C) are composed of almost pure calcite with a δ13C value of + 2.7‰ (relative to V-PDB) enabling classification as intermediate between thermometeogene and thermogene. In lower temperature water, away from the spring orifice, various amounts of aragonite (5-35%) with higher Sr concentrations precipitate from solution. This phenomenon is exceptional in hot spring carbonate deposits and could be explained by fast carbonate precipitation due to the morphology-related outgassing. Oxygen and hydrogen isotope measurements of the thermal water confirmed evaporation to be causing limited kinetic isotope fractionation. However, δ18O values of the travertine do show isotope shifts away from the equilibrium fractionation curve, which is most probably related to the rapid calcite precipitation and transportation along the flow path. Our data closely follow the temperature-Δ18Ocalcite-water relationship observed for other travertine localities. This is slightly displaced from the experimental curve and determines an empirical 'travertine curve'. Our study shows that this shift may result in an approximately 8 °C difference in paleotemperature calculations depending upon which fractionation curve is used.

Original languageEnglish
Pages (from-to)53-72
Number of pages20
JournalSedimentary Geology
Volume211
Issue number3-4
DOIs
Publication statusPublished - Nov 15 2008

Fingerprint

travertine
thermal water
stable isotope
fractionation
carbonate
oxygen isotope
calcite
isotope
chemical
hot water
hydrogen isotope
paleotemperature
thermal spring
aragonite
degassing
paleoclimate
carbon isotope
isotopic composition
water temperature
evaporation

Keywords

  • Carbonate microfacies
  • Hungary
  • Mineralogy
  • Non-equilibrium precipitation
  • Stable isotopes
  • Travertine

ASJC Scopus subject areas

  • Geology
  • Stratigraphy

Cite this

Chemical and stable isotope composition of recent hot-water travertines and associated thermal waters, from Egerszalók, Hungary : Depositional facies and non-equilibrium fractionation. / Kele, Sándor; Demény, A.; Siklósy, Zoltán; Németh, Tibor; Tóth, Mária; Kovács, Magdolna B.

In: Sedimentary Geology, Vol. 211, No. 3-4, 15.11.2008, p. 53-72.

Research output: Contribution to journalArticle

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AU - Kele, Sándor

AU - Demény, A.

AU - Siklósy, Zoltán

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AU - Tóth, Mária

AU - Kovács, Magdolna B.

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