69 D32. Geochemistry (Posters)

Sunday, 22 October 2017
9:00 AM - 5:30 PM
Halls 4EF


QUANTIFYING THE ∆63-∆47 OFFSET: DETERMINING MINERAL- AND TEMPERATURE-DEPENDENT ACID FRACTIONATION FACTORS THROUGH MASS SPECTROMETRIC ANALYSES OF STOCHASTICALLY-REORDERED CARBONATES

Paper number: 69-9
Program: Technical Sessions
Time: 9:00 AM – 5:30 PM


Authors


Abstract

“Clumped” isotope thermometry—the relationship between the formation temperature of a carbonate mineral and the relative abundance of 13C—18O bonds in its crystal lattice—is a novel geochemical proxy with a wide range of applications in paleoclimatology, geobiology, and paleoceanography. It is based on the thermodynamic propensity for rare, heavy isotopes to bond at greater rates at lower temperatures, while at high temperatures, a stochastic distribution of heavy isotopologues is achieved.

Unfortunately, precision mass spectrometric determination of the abundance of isotopologues in solid materials has proven difficult; instead, the isotopic composition of carbonates has traditionally been measured through acid digestion and subsequent analysis of the product CO2 gas. For example, clumped isotope thermometry typically relates formation temperature to ∆47, the abundance of 47-amu isotopologues relative to the predicted stochastic distribution.

As a consequence, the degree of fractionation that occurs between solid (∆63) and gaseous (∆47) phases has largely gone unstudied. By melting calcite and witherite powder at high pressures and temperatures (~1650ºC), we have produced a suite of carbonates predicted to have stochastic distributions of CO32- isotopologues (i.e., ∆63 values of 0‰). Thus, the measured ∆47 values of CO2 produced from these samples through acid digestion should equal the degree of fractionation that occurs.

We perform these measurements at a range of acid temperatures on several digestion apparatuses in order to deduce and quantify controls on acid digestion fractionation factors. We also calculate acid digestion fractionation factors using different sets of constants and compare our results to previously published estimates.


Geological Society of America Abstracts with Programs. Vol. 49, No. 6

doi: 10.1130/abs/2017AM-304811

© Copyright 2017 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.