| Paper No. 71-12 | ||
| Presentation Time: 11:15 AM-11:30 AM | ||
| OXYGEN ISOTOPE VALUES OF MODERN SPELEAN CARBONATES AND SOURCE WATERS: NON-EQUILIBRIUM DEPOSITION IS STATUS QUO | ||
|
TAYLOR, Penny M.1, CHAFETZ, Henry S.1, and GUIDRY, Sean Á.2, (1) Department of Geosciences, Univ of Houston, 312 Science and Research Building 1, Houston, TX 77204-5007, ptaylor@uh.edu, (2) ExxonMobile Production Company, Houston, TX Oxygen isotopic values of 35 modern calcite deposits and contemporaneous water samples from three Central Texas caves provide evidence that non-equilibrium deposition is common. All spelean sample pairs of calcite and immediately adjacent water are from streams and pools. Calcite precipitated on glass substrates, at the edge of pools, or on the water surface as floating rafts. Oxygen isotopic values range from –5.0 to –2.2 permil (PDB) and from -5.0 to 0.0 permil (SMOW) for calcite and water, respectively. Differences between theoretical and measured d18O values of these calcite samples range from –1.1 to +2.8 permil (mean=0.5; s=1.01; n=35). The temperature of the water from which a carbonate precipitated can be calculated assuming: 1) oxygen isotopic composition of the water, and 2) equilibrium fractionation between mineral and water. To assess the effect of observed disequilibrium fractionation on temperature calculations, the actual d18O values for carbonate and water sample pairs were used to calculate water temperature, treating temperature as an unknown. The resulting discrepancies ranged from –3.7 to +12.3°C relative to field-measured temperatures (mean=3.2; s=4.4; n=31). Evidence for non-equilibrium calcite deposition in three Central Texas caves is in agreement with data from a travertine-depositing stream within the same karst region as well as 6 carbonate-depositing surface streams from other areas (both ambient- and thermal-temperature) from which sample pairs of carbonate (aragonite and calcite) and water were analyzed. Without exception, non-equilibrium deposition is most common in these systems in California, Colorado, Oklahoma, Texas, Wyoming, and Italy. Collectively, these data provide strong evidence that equilibrium fractionation of oxygen isotopes is rare in these terrestrial environments. Thus, poor results from temperature calculations, using detailed isotope data (no assumptions) from natural systems, emphasize the potential for errors in interpretation of ancient depositional or climatic conditions. | ||
|
2002 Denver Annual Meeting (October 27-30, 2002)
| ||
| Session No. 71 Rivers in Karst: Processes and Applications Colorado Convention Center: A205 8:00 AM-12:00 PM, Monday, October 28, 2002 | ||
© Copyright 2002 The Geological Society of America (GSA), all rights reserved. Permission is hereby granted to the author(s) of this abstract to reproduce and distribute it freely, for noncommercial purposes. Permission is hereby granted to any individual scientist to download a single copy of this electronic file and reproduce up to 20 paper copies for noncommercial purposes advancing science and education, including classroom use, providing all reproductions include the complete content shown here, including the author information. All other forms of reproduction and/or transmittal are prohibited without written permission from GSA Copyright Permissions. | ||