Abstract
Abstract. A new chemistry module that simulates atmospheric ammonia (NH3) and ammonium (NH+4) was incorporated into a backward-in-time stochastic Lagrangian air quality model (STILT-Chem) that was originally developed to simulate the concentrations of a variety of gas-phase species at receptors. STILT-Chem simulates the transport of air parcels backward in time using ensembles of fictitious particles with stochastic motions, while accounting for emissions, deposition and chemical transformation forward in time along trajectories identified by the backward-in-time simulations. The incorporation of the new chemistry module allows the model to simulate not only gaseous species, but also multi-phase species involving NH3 and NH+4. The model was applied to simulate concentrations of NH3 and particulate NH+4 at six sites in the Canadian province of Ontario for a six-month period in 2006. The model-predicted concentrations of NH3 and particulate NH+4 were compared with observations, which show broad agreement between simulated concentrations and observations. Since the model is based on back trajectories, the influence of each major process such as emission, deposition and chemical conversion on the concentration of a modeled species at a receptor can be determined for every upstream location at each time step. This makes it possible to quantitatively investigate the upstream processes affecting receptor concentrations. The modeled results suggest that the concentrations of NH3 at those sites were significantly and frequently affected by Ohio, Iowa, Minnesota, Michigan, Wisconsin, southwestern Ontario and nearby areas. NH3 is mainly contributed by emission sources whereas particulate NH+4 is mainly contributed by the gas-to-aerosol chemical conversion of NH3. Dry deposition is the largest removal process for both NH3 and particulate NH+4. This study revealed the contrast between agricultural versus forest sites. Not only were emissions of NH3 higher, but removal mechanisms (especially chemical loss for NH3 and dry deposition for NH+4) were less efficient for agricultural sites. This combination explains the significantly higher concentrations of NH3 and particulate NH+4 observed at agricultural sites.
Highlights
Ammonia (NH3) is the primary basic gas in the atmosphere
Due to the stochastic nature of particle trajectories, the accuracy of Stochastic Time-Inverted Lagrangian Transport model (STILT)-Chem is affected by the number of particles used
Only a finite number of particles can be simulated due to limited computational resources. This leads to incomplete sampling of trajectory pathways and emissions, resulting in fluctuations in simulated concentrations
Summary
Ammonia (NH3) is the primary basic gas in the atmosphere. NH3 acts as a major agent in neutralizing acids in the atmosphere and plays an important role in aerosol formation. NH3 has major impacts on human health, acid deposition, atmospheric visibility, and radiative forcing. The significant sources of NH3 are animal waste, ammonification of humus followed by emission from soils, losses of NH3-based fertilizers from soils, and industrial emissions (Asman et al, 1998). NH3 is subject to transport and diffusion, removal by dry and wet deposition, and transformation to aerosol-bound NH+4 in reactions with acid gases and aerosols. Excessive deposition of atmospheric NH3 and NH+4 may lead to soil acidification and damage to sensitive species and ecosystem health (van Bremen et al, 1982; Morris, 1991)
Sign-in/Register to view highlights & summary Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
