2 research outputs found

    Fossil Fuel Combustion-Related Emissions Dominate Atmospheric Ammonia Sources during Severe Haze Episodes: Evidence from <sup>15</sup>N‑Stable Isotope in Size-Resolved Aerosol Ammonium

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    The reduction of ammonia (NH<sub>3</sub>) emissions is urgently needed due to its role in aerosol nucleation and growth causing haze formation during its conversion into ammonium (NH<sub>4</sub><sup>+</sup>). However, the relative contributions of individual NH<sub>3</sub> sources are unclear, and debate remains over whether agricultural emissions dominate atmospheric NH<sub>3</sub> in urban areas. Based on the chemical and isotopic measurements of size-resolved aerosols in urban Beijing, China, we find that the natural abundance of <sup>15</sup>N (expressed using δ<sup>15</sup>N values) of NH<sub>4</sub><sup>+</sup> in fine particles varies with the development of haze episodes, ranging from −37.1‰ to −21.7‰ during clean/dusty days (relative humidity: ∼ 40%), to −13.1‰ to +5.8‰ during hazy days (relative humidity: 70–90%). After accounting for the isotope exchange between NH<sub>3</sub> gas and aerosol NH<sub>4</sub><sup>+</sup>, the δ<sup>15</sup>N value of the initial NH<sub>3</sub> during hazy days is found to be −14.5‰ to −1.6‰, which indicates fossil fuel-based emissions. These emissions contribute 90% of the total NH<sub>3</sub> during hazy days in urban Beijing. This work demonstrates the analysis of δ<sup>15</sup>N values of aerosol NH<sub>4</sub><sup>+</sup> to be a promising new tool for partitioning atmospheric NH<sub>3</sub> sources, providing policy makers with insights into NH<sub>3</sub> emissions and secondary aerosols for regulation in urban environments

    Identifying Ammonia Hotspots in China Using a National Observation Network

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    The limited availability of ammonia (NH<sub>3</sub>) measurements is currently a barrier to understanding the vital role of NH<sub>3</sub> in secondary aerosol formation during haze pollution events and prevents a full assessment of the atmospheric deposition of reactive nitrogen. The observational gaps motivated us to design this study to investigate the spatial distributions and seasonal variations in atmospheric NH<sub>3</sub> on a national scale in China. On the basis of a 1-year observational campaign at 53 sites with uniform protocols, we confirm that abundant concentrations of NH<sub>3</sub> [1 to 23.9 μg m<sup>–3</sup>] were identified in typical agricultural regions, especially over the North China Plain (NCP). The spatial pattern of the NH<sub>3</sub> surface concentration was generally similar to those of the satellite column concentrations as well as a bottom-up agriculture NH<sub>3</sub> emission inventory. However, the observed NH<sub>3</sub> concentrations at urban and desert sites were comparable with those from agricultural sites and 2–3 times those of mountainous/forest/grassland/waterbody sites. We also found that NH<sub>3</sub> deposition fluxes at urban sites account for only half of the emissions in the NCP, suggesting the transport of urban NH<sub>3</sub> emissions to downwind areas. This finding provides policy makers with insights into the potential mitigation of nonagricultural NH<sub>3</sub> sources in developed regions
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