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Danielle S. Boshers

Publications and source records attributed to Danielle S. Boshers.

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The influence of sample matrix on the accuracy of nitrite N and O isotope ratio analyses with the azide method

Rationale The isotope ratios of nitrogen ( 15 N/ 14 N) and oxygen ( 18 O/ 16 O) in nitrite (NO 2 − ) can be measured by conversion of the nitrite into nitrous oxide (N 2 O) with azide, followed by mass spectrometric analysis of N 2 O by gas chromatography isotope ratio mass spectrometry (GC/IRMS). While applying this method to brackish samples, we noticed that the N and O isotope ratio measurements of NO 2 − are highly sensitive to sample salinity and to the pH at which samples are preserved. Methods We investigated the influence of sample salinity and sample preservation pH on the N and O isotope ratios of the N 2 O produced from the reaction of NO 2 − with azide. The N 2 O isotope ratios were measured by GC/IRMS. Results Under the experimental reaction conditions, the conversion of NO 2 − into N 2 O was less complete in lower salinity solutions, resulting in respective N and O isotopic offsets of +2.5‰ and −14.0‰ compared with seawater solutions. Differences in salinity were also associated with differences in the fraction of O atoms exchanged between NO 2 − and water during the reaction. Similarly, aqueous NO 2 − samples preserved at elevated pH values resulted in the incomplete conversion of NO 2 − into N 2 O by azide, and consequent pH‐dependent isotopic offsets, as well as differences in the fraction of O atoms exchanged with water. The addition of sodium chloride to the reaction matrix of samples and standards largely mitigated salinity‐dependent isotopic offsets in the N 2 O product, and nearly homogenized the fraction of O atom exchange among samples of different salinity. A test of the hypobromite–azide method to measure N isotope ratios of ammonium by conversion into NO 2 − then N 2 O revealed no influence of sample salinity on the N isotope ratios of the N 2 O product. Conclusions We outline recommendations to mitigate potential matrix effects among samples and standards, to improve the accuracy of N and O isotope ratios in NO 2 − measured with the azide method.

Rapid Communications in Mass Spectrometry

Constraining the oxygen isotopic composition of nitrate produced by nitrification

Measurements of the stable isotope ratios of nitrogen ( 15 N/ 14 N) and oxygen ( 18 O/ 16 O) in nitrate (NO 3 – ) enable identification of sources, dispersal, and fate of natural and contaminant NO 3 – in aquatic environments. The 18 O/ 16 O of NO 3 – produced by nitrification is often assumed to reflect the proportional contribution of oxygen atom sources, water, and molecular oxygen, in a 2:1 ratio. Culture and seawater incubations, however, indicate oxygen isotopic equilibration between nitrite (NO 2 – ) and water, and kinetic isotope effects for oxygen atom incorporation, which modulate the NO 3 – 18 O/ 16 O produced during nitrification. To investigate the influence of kinetic and equilibrium effects on the isotopic composition of NO 3 – produced from the nitrification of ammonia (NH 3 ), we incubated streamwater supplemented with ammonium (NH 4 + ) and increments of 18 O-enriched water. Resulting NO 3 – 18 O/ 16 O ratios showed (1) a disproportionate sensitivity to the 18 O/ 16 O ratio of water, mediated by isotopic equilibration between water and NO 2 – , as well as (2) kinetic isotope discrimination during O atom incorporation from molecular oxygen and water. Empirically, the NO 3 – 18 O/ 16 O ratios thus produced fortuitously converge near the 18 O/ 16 O ratio of water. More elevated NO 3 – 18 O/ 16 O values commonly reported in soils and oxic groundwater may thus derive from processes additional to nitrification, including NO 3 – reduction.

Environmental Science & Technology