Journal of Geophysical Research Atmospheres · 2008 · 86 citations · 97 references
Natural SciencesEarth SciencesAtmospheric ChemistryAtmospheric ScienceBiogeochemistryCryosphere ClimatologyIce-atmosphere InteractionsNitrogen OxidesNitrogen Oxides ChemistrySnow ObservationSnow ScienceIce Core PaleoclimatologyIsotope Seasonality In SnowIsotopic Variability In SnowOxygen Isotope CompositionOxygen Isotope ProxiesOxygen Isotope RatiosOxygen Isotope SignaturesSnow Isotope Fractionation
We quantify controls on seasonal changes of the oxygen isotope anomaly of nitrate (Δ 17 O(NO 3 − ), wherein Δ 17 O ≈ δ 17 O − (0.52 × δ 18 O)) in snow at Summit, Greenland, in an effort to enable quantitative reconstructions of paleoatmospheric oxidant concentrations from ice core Δ 17 O(NO 3 − ). Measurements of Δ 17 O(NO 3 − ) from a snowpit at Summit are compared to calculations from an atmospheric chemical box model. Measured values of Δ 17 O(NO 3 − ) covering three seasonal cycles (January–December 2000, July 2003–March 2006) range from 22.4‰ in summertime to 33.7‰ in wintertime, while model results show a larger range (18.9–31.5‰). Agreement between observed and modeled results is excellent for winter, when O 3 oxidation of nitrogen oxides dominates nitrate production (winter averages agree within 0.3‰). The 2–7‰ discrepancy between summertime box model results and measurements of Δ 17 O(NO 3 − ) may result from several influences not accounted for by our box model, including nonzero Δ 17 O of OH over polar regions, stratospheric influence on surface O 3 at Summit, participation of BrO in nitrate production, and tropospheric transport of nitrate. A box model sensitivity study shows that annual mean Δ 17 O(NO 3 − ) is most sensitive to changes in the ratio of [O 3 ]/([HO 2 ] + [RO 2 ]) in summer.
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