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Updated: Nov 29, 2025

Sampling and Pretreatment of Tooth Enamel Carbonate for Stable Carbon and Oxygen Isotope Analysis
Published on: August 15, 2018
Designing working standards for stable H, C, and O isotope measurements in CO2 and H2 O
Jean-François Hélie1, Claude Hillaire-Marcel1
1Geotop & Département des sciences de la Terre et de l'atmosphère, Université du Québec à Montréal, Montreal, QC, Canada.
Rationale:
We address here the selection, preparation, calibration, storage, and use of carbonate and water working standards (WSs) for stable H, C, and O isotope measurements requiring the best possible precision and accuracy vs international reference materials (iRMs). This may be of interest for laboratories working intensively in the domains of the carbon and water cycles and of paleoclimate.
Methods:
Defining a WS for stable C and O isotope studies requires combining mineralogical, physical, chemical (low Mg- and trace-carbonate), and isotopic measurements to select a carbonate fit for purpose; for water, two distinct deionized or distilled waters, with high and low δ2 H and δ18 O values, respectively, are normally used. In both cases, a strict protocol must be followed to properly qualify the WS vs the current international isotopic scales, and much attention must be paid to calculating rigorous estimates of final uncertainties on these scales.
Results:
Two specific protocols for the selection of carbonate and water WSs are detailed. Equations for a proper estimate of uncertainties are proposed.
Conclusions:
The selection of WSs involves a preselection of potentially suitable materials based on initial estimates of their mineralogical, chemical, and isotopic properties and long-term stability, based on literature or previous measurements. Their precise characterization vs international isotopic scales requires a thorough analytical work in a correct sequence. When properly carried out, the proposed protocols should permit WSs to be obtained, defined vs the VSMOW and VPDB scales, with uncertainties comparable with those achieved for the characterization of iRMs.
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