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NRC Publications Archive Archives des publications du CNRCThis publication could be one of several versions: author's original, accepted manuscript or the publisher's version. / La version de cette publication peut être l'une des suivantes : la version prépublication de l'auteur, la version acceptée du manuscrit ou la version de l'éditeur. For the publisher's version, please access the DOI link below./ Pour consulter la version de l'éditeur, utilisez le lien DOI ci-dessous.http://doi.org/10.1039/b505545hJournal of Analytical Atomic Spectrometry, 20, 8, pp. 724-729, 2005 A mathematical approach to the accurate correction of the blank when applying isotope dilution (ID) and reverse ID is presented. The manner in which blank correction is undertaken is critical to the quality of the final results. Direct subtraction of a procedural blank from the gross analyte concentration is only valid when the blank contributes to the primary ID process and not to the reverse ID process. When the blank contributes to both processes, typically only a fraction of this blank concentration should be subtracted. The approach developed here was illustrated and validated by the determination of MeHg in tuna fish using ID and reverse ID SPME GC-ICP-MS and an enriched Me 198 Hg spike. Despite a 150-fold higher blank (equivalent to 7% of the analyte concentration in the sample) arising from use of a 1 M NaOAc/HOAc buffer solution compared to that obtained with use of a 0.5 M NH 4 OAc/HOAc buffer, final concentrations of 19.90 AE 0.34 and 19.88 AE 0.10 mmol kg À1 (one standard deviation, n ¼ 3) respectively, were derived. T...