Defining an absolute reference frame for 'clumped' isotope studies of CO2

Kate J. Dennis*, Hagit P. Affek, Benjamin H. Passey, Daniel P. Schrag, John M. Eiler

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

504 Scopus citations

Abstract

We present a revised approach for standardizing and reporting analyses of multiply substituted isotopologues of CO2 (i.e., 'clumped' isotopic species, especially the mass-47 isotopologues). Our approach standardizes such data to an absolute reference frame based on theoretical predictions of the abundances of multiply-substituted isotopologues in gaseous CO2 at thermodynamic equilibrium. This reference frame is preferred over an inter-laboratory calibration of carbonates because it enables all laboratories measuring mass 47 CO2 to use a common scale that is tied directly to theoretical predictions of clumping in CO2, regardless of the laboratory's primary research field (carbonate thermometry or CO2 biogeochemistry); it explicitly accounts for mass spectrometric artifacts rather than convolving (and potentially confusing) them with chemical fractionations associated with sample preparation; and it is based on a thermodynamic equilibrium that can be experimentally established in any suitably equipped laboratory using commonly available materials. By analyzing CO2 gases that have been subjected to established laboratory procedures known to promote isotopic equilibrium (i.e., heated gases and water-equilibrated CO2), and by reference to thermodynamic predictions of equilibrium isotopic distributions, it is possible to construct an empirical transfer function that is applicable to data with unknown clumped isotope signatures. This transfer function empirically accounts for the fragmentation and recombination reactions that occur in electron impact ionization sources and other mass spectrometric artifacts. We describe the protocol necessary to construct such a reference frame, the method for converting gases with unknown clumped isotope compositions to this reference frame, and suggest a protocol for ensuring that all reported isotopic compositions (e.g., Δ47 values; Eiler and Schauble, 2004; Eiler, 2007) can be compared among different laboratories and instruments, independent of laboratory-specific analytical or methodological differences. We then discuss the use of intra-laboratory secondary reference frames (e.g., based on carbonate standards) that can be more easily used to track the evolution of each laboratory's empirical transfer function. Finally, we show inter-laboratory reproducibility on the order of ±0.010 (1σ) for four carbonate standards, and present revised paleotemperature scales that should be used to convert carbonate clumped isotope signatures to temperature when using the absolute reference frame described here. Even when using the reference frame, small discrepancies remain between two previously published synthetic carbonate calibrations. We discuss possible reasons for these discrepancies, and highlight the need for additional low temperature (<15°C) synthetic carbonate experiments.

Original languageAmerican English
Pages (from-to)7117-7131
Number of pages15
JournalGeochimica et Cosmochimica Acta
Volume75
Issue number22
DOIs
StatePublished - 15 Nov 2011
Externally publishedYes

Bibliographical note

Funding Information:
This paper grew out of a discussion at the University of Washington’s Clumped Isotope Workshop held in Seattle, WA in April 2010, and would not have been possible without the open exchange of ideas and data between the four clumped isotope laboratories represented here. Dan Schrag and Kate Dennis thank Henry and Wendy Breck, and Shell Oil Company for funding, and Greg Eischeid and Marianna Verlage for laboratory assistance. Hagit Affek thanks the Earth System Center for Stable Isotope Studies of the Yale Institute for Biospheric Studies, with funding by NSF-EAR-0842482 . Shikma Zaarur is also acknowledged for her insights to the discussion of synthetic carbonate calibrations. Ben Passey was funded by the American Chemical Society PRF#50321-DNI2, and thanks Gregory Henkes and Marina Suarez for assistance in the laboratory. John Eiler was funded by the National Science Foundation . We thank Zhengrong Wang for providing equilibrium clumped isotope compositions for gas phase CO 2 based on his theoretical models ( Wang et al., 2004 ). We also thank Kyger C. Lohmann and Shuhei Ono for their thorough reviews, both of which helped make this paper more transparent. We also acknowledge an anonymous reviewer, and the Associate Editor, Edwin Schauble.

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