|2011 GSA Annual Meeting in Minneapolis (9–12 October 2011)|
|Paper No. 58-1|
|Presentation Time: 1:35 PM-1:50 PM|
EXPERIMENTAL DETERMINATION OF MG ISOTOPE FRACTIONATION DURING PRECIPITATION OF INORGANIC CALCITE
LI, Weiqiang1, CHAKRABORTY, Suvankar2, BEARD, Brian L.1, JOHNSON, Clark M.1, and ROMANEK, Christopher S.2, (1) Department of Geoscience, University of Wisconsin-Madison, NASA Astrobiology Institute, 1215 W. Dayton St, Madison, WI 53706, firstname.lastname@example.org, (2) Department of Earth and Environmental Sciences, University of Kentucky, Lexington, KY 40506|
The isotopic composition of Mg in biogenic and inorganic carbonate is of great interest in studies of paleoclimate and paleooceanography because of the potential for constraining temperatures, vital effects, and marine Mg fluxes. Growth of carbonate skeletons in marine organisms produces a wide range of isotopic compositions that are species dependent, where Δ26/24Mgcarb-sol fractionations vary from -1 to -5 ‰ (e.g, Hippler et al., 2009 GCA). Constraining the Mg isotope fractionation during inorganic carbonate precipitation is important because this serves as the baseline for interpreting the Mg isotope compositions of biogenic samples. In this study we report Mg isotope fractionation factors between Mg-bearing calcite and Mg-Ca solutions under laboratory conditions. Eighteen free-drift synthesis experiments of carbonate were carried out at temperatures between 4 ºC and 45 ºC, using solutions with Mg:Ca molar ratio between 3:1 and 18:1, buffered at PCO2 between 0.038% and 3%. Pure CaCO3 seed crystals were used to promote the heterogeneous growth of solid form solution in the experiments and to reduce kinetic isotope effects associated with nucleation and crystallization. Under such conditions, calcite overgrowths that contained 1.28-14.9 mole percent Mg precipitated on the seed crystals over 1 to 58 days. The Mg isotope composition of Mg-bearing calcite and Mg-Ca solutions were measured to a precision of ±0.15‰ (2sd) in δ26/24Mg after careful purification of these Ca-rich materials using multiple ion-exchange separation techniques. The measured Mg isotope fractionation factors between Mg-calcite and solution (Δ26/24Mgcal-sol) show a systematic and discernable temperature dependence, changing from -2.26 ‰ at 45 ºC to -2.76 ‰ at 4 ºC. The fractionation factors are not correlated with Mg content of the Mg-calcite overgrowth, PCO2, or the composition of the Mg-Ca solution. A chemostat experiment was done conducted at 22 ºC, where the solution composition was maintained under steady-state conditions. The measured Δ26/24Mgcarb-sol fractionation factor for the chemostat experiment is -2.54 ‰, which is identical within error to the 3 free drift experiments conducted at the same temperature.
2011 GSA Annual Meeting in Minneapolis (9–12 October 2011)
General Information for this Meeting
|Session No. 58|
Advances in Terrestrial Paleoclimatology and Paleoecology: Geochemical Techniques and Examples Using Inorganic and Organic Molecules in Fossil Soils, Plants, Invertebrates, and Vertebrates I
Minneapolis Convention Center: Room 200FG
1:30 PM-5:30 PM, Sunday, 9 October 2011
Geological Society of America Abstracts with Programs, Vol. 43, No. 5, p. 162
© Copyright 2011 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.