SI-traceable certification of methylmercury amount content in a tuna material

Speciation analysis has an ever-increasing relevance in environmental studies, for risk assessment and, eventually, for legislation. There is a concomitant need for reliability and comparability of speciation measurements made at different places and at different times, to assist with which the concepts of traceability ( to a stated system of reference) and combined uncertainty budgetting can be applied. Traceability can be visualised as a chain, or a combination of chains, between a measurement result and a reference where each link in the chain(s) is a mathematical expression representing our best understanding of a measurement process, within a declared level of uncertainty. The combined uncertainty of the measurement result is calculated by combination of the uncertainties associated with each parameter of the traceability chain. This also helps method optimisation and in the diagnosis of possible errors in results by highlighting components that contribute significant uncertainty, provided that an appropriate uncertainty was attached to each parameter afflecting the result. This work shows how a methylmercury, MeHg, measurement was made, and how understanding of the measurement process could make the result reliable and comparable to results between laboratories. The measurement process was validated according ISO 17025 through the use of reference materials for calibration, comparison of results with different methods, a systematic assessment of factors influencing the result, by calculating the combined measurement uncertainty and by participation in an inter-laboratory comparison. A tuna material was distributed for the laboratory inter-comparison studies for the Comite Consultatif pour la Quantite de Matiere (CCQM) pilot study 39 and International Measurement Evaluation Programme (IMEP) comparison 20. MeHg was measured using species-specific isotope dilution, SSID, by blending samples with an isotopic certified reference material, ERM(R)AE670, which contains CH(3)HgCl isotopically enriched in (202)Hg, followed by extraction and derivatisation of Hg species and detection by gas chromatography-inductively coupled plasma mass spectrometry. SSID was applied to provide mass fractions traceable to the SI through the comparison of isotope ratios measured in blends prepared by metrological weighing, with reference materials carrying values traceable to the SI. Uncertainties associated with each of the experimental steps were investigated and combined according to ISO guidelines. The mass fraction of Hg in the form of MeHg in the tuna sample carried an expanded combined uncertainty estimated at 5.6% (k = 2). The greatest uncertainty contributions stemmed from the degree to which sample + spike equilibration could be proved, the certified MeHg content of the spike material and (for the IMEP-20 value) sample homogeneity. Uncertainty contributions from the known natural Hg isotopic composition, isotope ratio measurement and instrumental correction factors were minor in comparison. The level of equivalence was demonstrated by CCQM-P39 in that the standard deviation of mass fractions reported by 9 participating laboratories that applied SSID was 2.6%, and the IRMM value lay 0.24% from the mean.