Paper No. 8-0
ISOTOPIC COMPOSITION OF PALEOPRECIPITATION FROM FLUID INCLUSIONS IN SPELEOTHEM CALCITE
SEREFIDDIN, Feride, Geography and Geology, McMaster Univ, 1280 Main Street West, Hamilton, ON L8S4M1, Canada, serefif@mcmaster.ca, SCHWARCZ, Henry Philip, McMaster Univ, 1280 Main St W, Hamilton, ON L8S 4M1, Canada, and FORD, Derek C., School of Geography and Geology, McMaster Univ, Hamilton, L8S4K1, Canada

Improvements in the extraction of microinclusion water from speleothem calcite make possible multiple, higher resolution measurements of dD of water. This can be applied to paleoclimate reconstruction using d18O and d13C of speleothems. Additionally, analysis of lattice-bound water may provide an additional paleothermometer. Two speleothems from Reed's Cave, South Dakota that grew during the Wisconsin glacial period from marine isotope stages 4 to 2 (65 –23 kya) were analyzed to determine the isotopic composition of paleoprecipitation. Paleotemperatures are calculated using O-isotope fractionation between calcite and water. The oxygen isotopes of fluid inclusion water cannot be measured directly because of post-depositional exchange of oxygen molecules between the host calcite and the fluid inclusions. The isotopic compositions of cave dripwaters approximate average annual d18O and d D of precipitation (Yonge et al .1983), therefore d18O can be calculated from D/H of inclusion water using the MWL relationship d D=8 d18O + 10.

FTIR analysis shows that even after removal of microinclusions, a strong water signal still exists. High temperature calcination of calcite to CaO + CO2 releases this crystal-bound water. Isotopic (D/H) fractionation between bound and inclusion water may yield a paleotemperature record. Also, the presence of this component in water released at high temperatures may explain a -20‰ offset observed by some researchers.

GSA Annual Meeting, November 5-8, 2001
General Information for this Meeting
Session No. 8
Paleoclimatology/Paleoceanography I
Hynes Convention Center: 103
8:00 AM-12:00 PM, Monday, November 5, 2001
 

© Copyright 2001 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.