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Shipboard analytical intercomparison of dissolved iron in surface waters along a north-south transect of the Atlantic Ocean
Citation
Bowie, AR and Achterberg, EP and Blain, S and Boye, M and Croot, PL and de Baar, HJW and Laan, P and Sarthou, G and Worsfold, PJ, Shipboard analytical intercomparison of dissolved iron in surface waters along a north-south transect of the Atlantic Ocean, Marine Chemistry, 84, (1-2) pp. 19-34. ISSN 0304-4203 (2003) [Refereed Article]
DOI: doi:10.1016/S0304-4203(03)00091-4
Abstract
A shipboard analytical intercomparison of dissolved (<0.2 μm) iron in the surface waters of the Atlantic Ocean was undertaken during October 2000. A single underway surface (1-2 m) seawater sampling and filtration protocol was used, in order to minimise differences from possible sample contamination. Over 200 samples (1/h) were collected over 12 days and analysed immediately using four different analytical methods, based on three variants of flow injection with luminol chemiluminescence (FI-CL) and cathodic stripping voltammetry (CSV). Dissolved iron concentrations varied between 0.02 and 1.61 nM during the intercomparison. On average, CSV [Electroanalysis 12 (2000) 565] measured 0.08 nM higher iron concentrations than one FI-CL method [Anal. Chim. Acta 361 (1998) 189], which measured 0.13 nM higher iron values than the other two [Anal. Chem. 65 (1993) 1524; Anal. Chim. Acta 377 (1998) 113], Statistical analyses (paired two-tailed t-test) showed that each analytical method gave significantly different dissolved iron concentrations at the 95% confidence interval. These data however, represent a significant improvement over earlier intercomparison exercises for iron. The data have been evaluated with respect to accuracy and overall inter-laboratory replicate precision, which was generally better than the 95% confidence intervals reported for the NASS Certified Reference Materials. Systematic differences between analytical methods were probably due to the extraction of different physico-chemical forms of iron during preconcentration, either on the micro-column resin (in the FI methods) or with competing ligand equilibration (in the CSV method). Small systematic concentration differences may also have resulted from protocols used for quantification of the analytical blank and instrument calibration. © 2003 Elsevier B.V All rights reserved.
Item Details
| Item Type: | Refereed Article |
|---|---|
| Research Division: | Earth Sciences |
| Research Group: | Oceanography |
| Research Field: | Chemical Oceanography |
| Objective Division: | Environment |
| Objective Group: | Physical and Chemical Conditions of Water |
| Objective Field: | Physical and Chemical Conditions of Water in Marine Environments |
| UTAS Author: | Bowie, AR (Associate Professor Andrew Bowie) |
| ID Code: | 32013 |
| Year Published: | 2003 |
| Web of Science® Times Cited: | 31 |
| Deposited By: | Chemistry |
| Deposited On: | 2004-08-01 |
| Last Modified: | 2005-03-15 |
| Downloads: | 0 |
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