Technical Note: Evaluation of between-sample memory effects in the analysis of [delta]2H and [delta]18O of water samples measured by laser spectroscopes

This study evaluated between-sample memory in isotopic measurements of δ2 H and δ18 O in water samples by laser spectroscopy. Ten isotopically depleted water samples spanning a broad range of oxygen and hydrogen isotopic compositions were measured by three generations of off-axis integrated cavity o...

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Veröffentlicht in:Hydrology and earth system sciences 2012-10, Vol.16 (10), p.3925
Hauptverfasser: Penna, D, Stenni, B, Sanda, M, Wrede, S, Bogaard, T A, Michelini, M, Fischer, B M. C, Gobbi, A, Mantese, N, Zuecco, G, Borga, M, Bonazza, M, Sobotková, M, cejková, B, Wassenaar, L I
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Sprache:eng
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Zusammenfassung:This study evaluated between-sample memory in isotopic measurements of δ2 H and δ18 O in water samples by laser spectroscopy. Ten isotopically depleted water samples spanning a broad range of oxygen and hydrogen isotopic compositions were measured by three generations of off-axis integrated cavity output spectroscopy and cavity ring-down spectroscopy instruments. The analysis procedure encompassed small (less than 2[per thousand] for δ2 H and 1[per thousand] for δ18 O) and large (up to 201[per thousand] for δ2 H and 25[per thousand] for δ18 O) differences in isotopic compositions between adjacent sample vials. Samples were injected 18 times each, and the between-sample memory effect was quantified for each analysis run. Results showed that samples adversely affected by between-sample isotopic differences stabilised after seven-eight injections. The between-sample memory effect ranged from 14% and 9% for δ2 H and δ18 O measurements, respectively, but declined to negligible carryover (between 0.1% and 0.3% for both isotopes) when the first ten injections of each sample were discarded. The measurement variability (range and standard deviation) was strongly dependent on the isotopic difference between adjacent vials. Standard deviations were up to 7.5[per thousand] for δ2 H and 0.54[per thousand] for δ18 O when all injections were retained in the computation of the reportable δ-value, but a significant increase in measurement precision (standard deviation in the range 0.1[per thousand]-1.0[per thousand] for δ2 H and 0.05[per thousand]-0.17[per thousand] for δ18 O) was obtained when the first eight injections were discarded. In conclusion, this study provided a practical solution to mitigate between-sample memory effects in the isotopic analysis of water samples by laser spectroscopy.
ISSN:1027-5606
1607-7938
DOI:10.5194/hess-16-3925-2012