Abstract
Across many environments, nitrate (\(\mbox{NO}_{3}^-\)) is an important form of N available for microorganisms and photosynthetic organisms. Accurate \(\mbox{NO}_{3}^-\) measurements are important for examining N cycling and retention in terrestrial and aquatic ecosystems, but a common method of \(\mbox{NO}_{3}^-\) analysis can underestimate \(\mbox{NO}_{3}^-\) concentrations when soluble iron is present (iron > 10 mg L − 1). The basic method is robust, using copperized cadmium to reduce \(\mbox{NO}_{3}^-\) and then diazotizing the resulting \(\mbox{NO}_{2}^-\) in a two-step process to form an easily measured colored product. We show that iron interference is unique to using an NH4Cl and ethylenediaminetetraacetic acid (EDTA) buffer. We hypothesize that interference is through iron-catalyzed reduction of the intermediate color product, a diazonium ion. We examine three historical buffers as alternatives to NH4Cl/EDTA and recommend replacement of EDTA with diethylenetriaminepentaacetic acid, which chelates metals much like EDTA, but unlike EDTA, it does not cause interference in the presence of iron.
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An erratum to this article can be found at http://dx.doi.org/10.1007/s10661-010-1440-5
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Colman, B.P. Understanding and eliminating iron interference in colorimetric nitrate and nitrite analysis. Environ Monit Assess 165, 633–641 (2010). https://doi.org/10.1007/s10661-009-0974-x
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DOI: https://doi.org/10.1007/s10661-009-0974-x