EGU26-18181, updated on 14 Mar 2026
https://doi.org/10.5194/egusphere-egu26-18181
EGU General Assembly 2026
© Author(s) 2026. This work is distributed under
the Creative Commons Attribution 4.0 License.
Oral | Tuesday, 05 May, 14:55–15:05 (CEST)
 
Room 1.85/86
Historical Changes and Drivers of Aerosol Acidity in Switzerland under emission reduction and its implication of regulation policies
Jun Zhang1, Ali Waseem1, Andrea Baccarini1, Stylianos Kakavas2, Christoph Hüglin3, and Athanasios Nenes1,4
Jun Zhang et al.
  • 1Laboratory of Atmospheric Processes and their Impacts (LAPI), Ecole Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland
  • 2Institute of Chemical Engineering Sciences, Foundation for Research and Technology Hellas (FORTH/ICE-HT), Patras, Greece
  • 3Empa, Swiss Federal Laboratories for Materials Science and Technology, 8600 Dübendorf, Switzerland
  • 4Laboratory of Atmospheric Processes and their Impacts, Institute of Chemical Engineering Sciences, Foundation for Research and Technology Hellas, Patras, Greece

Emission controls in Europe have substantially reduced SOx and NOx but left NH3 largely unchanged. This imbalance between acidic and basic species may shift aerosol acidity and its impacts, including toxicity, particulate matter (PM) composition, and the deposition of reactive nitrogen (Nr). The atmospheric deposition of Nr plays a critical role in ecosystem productivity and PM formation, with impacts that vary across spatial and temporal scales.

In this study, long-term observations (2008–2024) of atmospheric gases and aerosols from Swiss monitoring sites ware analyzed to assess changes under current emission reductions. Aerosol pH was estimated using the ISORROPIA-lite thermodynamic model1 and interpreted using SHapley Additive exPlanations (SHAP) to quantify key drivers. Annual mean aerosol pH shows a slight increasing trend, with consistently lower values in summer than in winter. SHAP results indicate that temperature controls seasonal pH variability at agricultural sites, whereas total ammonia (NH3T) dominates at the semi-alpine site.

Dry deposition regimes of HNO3 and NH3 were investigated in relation to aerosol liquid water content and acidity following the approach of Nenes et al. (2021).2 The findings indicate that NH3 deposition is rapid across both the lowland and Alpine regions, suggesting localized nitrogen burdens near emission sources. In contrast, PM has become increasingly insensitive to NH3 and more sensitive to HNO3, particularly in the agricultural sites. These results highlight that, although HNO3 precursor controls have effectively reduced PM pollution without the need for NH3 reductions, evermore significant ecological concerns remain from a lack of NH3 control. This underscores the need for coordinated reductions in both NOx and NH3 emissions.

References:

1 Kakavas, S., Pandis, S. N., and Nenes, A.: ISORROPIA-Lite: A Comprehensive Atmospheric Aerosol Thermodynamics Module for Earth System Models, Tellus B: Chemical and Physical Meteorology, 74, DOI: 10.16993/tellusb.33, 2022.

2 Nenes, A., Pandis, S. N., Kanakidou, M., Russell, A. G., Song, S., Vasilakos, P., and Weber, R. J.: Aerosol acidity and liquid water content regulate the dry deposition of inorganic reactive nitrogen, Atmospheric Chemistry and Physics, 21, 6023–6033 DOI:10.5194/acp-21-6023-2021, 2021.

How to cite: Zhang, J., Waseem, A., Baccarini, A., Kakavas, S., Hüglin, C., and Nenes, A.: Historical Changes and Drivers of Aerosol Acidity in Switzerland under emission reduction and its implication of regulation policies, EGU General Assembly 2026, Vienna, Austria, 3–8 May 2026, EGU26-18181, https://doi.org/10.5194/egusphere-egu26-18181, 2026.