A community-wide intercomparison exercise for the determination of dissolved iron in seawater

Bowie, A.R., Achterberg, E.P., Croot, P.L., de Baar, H.J.W., Laan, P., Moffett, J.W., Ussher, S.J. and Worsfold, P.J. (2006) A community-wide intercomparison exercise for the determination of dissolved iron in seawater. Marine Chemistry, 98, (1), 81-99. (doi:10.1016/j.marchem.2005.07.002).


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The first large-scale international intercomparison of analytical methods for the determination of dissolved iron in seawater was carried out between October 2000 and December 2002. The exercise was conducted as a rigorously “blind” comparison of 7 analytical techniques by 24 international laboratories. The comparison was based on a large volume (700 L), filtered surface seawater sample collected from the South Atlantic Ocean (the “IRONAGES” sample), which was acidified, mixed and bottled at sea. Two 1-L sample bottles were sent to each participant. Integrity and blindness were achieved by having the experiment designed and carried out by a small team, and overseen by an independent data manager. Storage, homogeneity and time-series stability experiments conducted over 2.5 years showed that inter-bottle variability of the IRONAGES sample was good (< 7%), although there was a decrease in iron concentration in the bottles over time (0.8–0.5 nM) before a stable value was observed. This raises questions over the suitability of sample acidification and storage.

For the complete dataset of 45 results (after excluding 3 outliers not passing the screening criteria), the mean concentration of dissolved iron in the IRONAGES sample was 0.59 ± 0.21 nM, representing a coefficient of variation (%CV) for analytical comparability (“community precision”) of 36% (1s), a significant improvement over earlier exercises. Within-run precision (5–10%), inter-run precision (15%) and inter-bottle homogeneity (< 7%) were much better than overall analytical comparability, implying the presence of: (1) random variability (inherent to all intercomparison exercises); (2) errors in quantification of the analytical blank; and (3) systematic inter-method variability, perhaps related to secondary sample treatment (e.g. measurement of different physicochemical fractions of iron present in seawater) in the community dataset. By grouping all results for the same method, analyses performed using flow injection-luminol chemiluminescence (with FeII detection after sample reduction) [Bowie, A.R., Achterberg, E.P., Mantoura, R.F.C., Worsfold, P.J., 1998. Determination of sub-nanomolar levels of iron in seawater using flow injection with chemiluminescence detection. Anal. Chim. Acta 361, 189–200] and flow injection-catalytic spectrophotometry (using the reagent DPD) [Measures, C.I., Yuan, J., Resing, J.A., 1995. Determination of iron in seawater by flow injection analysis using in-line preconcentration and spectrophotometric detection. Mar. Chem. 50, 3–12] gave significantly (P = 0.05) higher dissolved iron concentrations than analyses performed using isotope dilution ICPMS [Wu, J.F., Boyle, E.A., 1998. Determination of iron in seawater by high-resolution isotope dilution inductively coupled plasma mass spectrometry after Mg(OH)2 co-precipitation. Anal. Chim. Acta 367, 183–191]. There was, however, evidence of scatter within each method group (CV up to 59%), implying that better uniformity in procedures may be required. This paper does not identify individual data and should not be viewed as an evaluation of single laboratories. Rather it summarises the status of dissolved iron analysis in seawater by the international community at the start of the 21st century, and can be used to inform future exercises including the SAFE iron intercomparison study in the North Pacific in October 2004.

Item Type: Article
ISSNs: 0304-4203 (print)
Related URLs:
Keywords: Iron, seawater, determination, intercomparison, ironages, large volume sample
Subjects: Q Science > QD Chemistry
G Geography. Anthropology. Recreation > GC Oceanography
Divisions: University Structure - Pre August 2011 > School of Ocean & Earth Science (SOC/SOES)
ePrint ID: 38073
Date Deposited: 01 Jun 2006
Last Modified: 27 Mar 2014 18:24
URI: http://eprints.soton.ac.uk/id/eprint/38073

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