i_NRACM: incorporating ¹⁵N into the Regional Atmospheric Chemistry Mechanism (RACM) for assessing the role photochemistry plays in controlling the isotopic composition of NO_<i>x</i>, NO_<i>y</i>, and atmospheric nitrate

Nitrogen oxides, classified as NOx (nitric oxide (NO) + nitrogen dioxide (NO2)) and NOy (NOx+ NO3, N2O5 HNO3, + HNO4+ HONO + Peroxyacetyl nitrate (PAN) + organic nitrates + any oxidized N compound), are important trace gases in the troposphere, which play an important role in the formation of ozone, particulate matter (PM), and secondary organic aerosols (SOA). There remain many uncertainties in the origin and fate of atmospheric N compounds including the understanding of NOy cycling, NOx emission budgets, unresolved issues within the heterogeneous uptake coefficients of N2O5, and the formation of organic nitrates in urban forests, to name a few. A potential tool to resolve some of these uncertainties are using natural abundance N isotopes in NOy compounds. Here we have developed a photochemical mechanism used to simulate tropospheric photochemistry to include 15N compounds and reactions as a means to simulate δ15N values in NOy compounds. The 16 N compounds and 96 reactions involving N used in the Regional Atmospheric Chemistry Mechanism (RACM) were replicated using 15N in a new mechanism called iNRACM. The 192 N reactions in iNRACM were tested to see if isotope effects were relevant with respect to significantly changing the δ15N values (±1 ‰) of NOx, HONO, and/or HNO3. The isotope fractionation factors (α) for relevant reactions were assigned based on recent experimental or calculated values. Each relevant reaction in the iNRACM mechanism was tested individually and in concert in order to assess the controlling reactions. The controlling reactions and their diurnal importance are discussed. A comparison between iNRACM predictions and observed δ15N NO3- in particulate matter from Tucson, Arizona, suggests the model, and isotope fractionation factors incorporated into it, are accurately capturing the isotope effects occurring during the photochemistry of NOy. The implication is that measurements of δ15N in NOy compounds may be a new way of tracing in situ N chemistry and a means of assessing NOx emission budgets.

The importance of alkyl nitrates and sea ice emissions to atmospheric NO_x sources and cycling in the summertime Southern Ocean marine boundary layer

Atmospheric nitrate originates from the oxidation of nitrogen oxides (NOx = NO + NO2) and impacts both tropospheric chemistry and climate. NOx sources, cycling, and NOx to nitrate formation pathways are poorly constrained in remote marine regions, especially the Southern Ocean where pristine conditions serve as a useful proxy for the preindustrial atmosphere. Here, we measured the isotopic composition (δ15N and δ18O) of atmospheric nitrate in coarse-mode (> 1 μm) aerosols collected in the summertime marine boundary layer of the Atlantic Southern Ocean from 34.5° S to 70° S, and across the northern edge of the Weddell Sea. The δ15N-NO3− decreased with latitude from −2.7 ‰ to −43.1 ‰. The decline in δ15N with latitude is attributed to changes in the dominant NOx sources: lightning at the low latitudes, oceanic alkyl nitrates at the mid latitudes, and photolysis of nitrate in snow at the high latitudes. There is no evidence of any influence from anthropogenic NOx sources or equilibrium isotopic fractionation. Using air mass back trajectories and an isotope mixing model, we calculate that oceanic alkyl nitrate emissions have a δ15N signature of −22.0 ‰ ± 7.5 ‰. Given that measurements of alkyl nitrate contributions to remote nitrogen budgets are scarce, this may be a useful tracer for detecting their contribution in other oceanic regions. The δ18O-NO3− was always less than 70 ‰, indicating that daytime processes involving OH are the dominant NOx oxidation pathway during summer. Unusually low δ18O-NO3− values (less than 31 ‰) were observed at the western edge of the Weddell Sea. The air mass history of these samples indicates extensive interaction with sea ice covered ocean, which is known to enhance peroxy radical production. The observed low δ18O-NO3− is therefore attributed to increased exchange of NO with peroxy radicals, which have a low δ18O, relative to ozone, which has a high δ18O. This study reveals that the mid- and high-latitude surface ocean may serve as a more important NOx source than previously thought, and that the ice-covered surface ocean impacts the reactive nitrogen budget as well as the oxidative capacity of the marine boundary layer.