Vegetation removes tropospheric ozone through stomatal uptake, and accurately modeling the stomatal uptake of ozone is important for modeling dry deposition and air quality. We evaluated the stomatal component of ozone dry deposition modeled by atmospheric chemistry models at six sites. We find that models and observation-based estimates agree at times during the growing season at all sites, but some models overestimated the stomatal component during the dry summers at a seasonally dry site.

A primary sink of air pollutants is dry deposition. Dry deposition estimates differ across the models used to simulate atmospheric chemistry. Here, we introduce an effort to examine dry deposition schemes from atmospheric chemistry models. We provide our approach’s rationale, document the schemes, and describe datasets used to drive and evaluate the schemes. We also launch the analysis of results by evaluating against observations and identifying the processes leading to model–model differences.

We considered it important to complete the content knowledge of secondary school physics with those concerning atmospheric humidity, fog, and air pollution. For this aim, a three-hour teaching module was elaborated, which included the analysis of the air-polluting events together with the foggy weather. The experimental curriculum motivated the students to understand processes that take place in their environment regarding environmental protection.

Motor vehicle road traffic in Budapest was reduced by approximately 50% of its ordinary level due to COVID-19. In parallel, concentrations of most criteria air pollutants declined by 30–60%. Change rates of NO and NO₂ with relative change in traffic intensity were the largest, total particle number concentration showed considerable dependency, while particulate matter mass concentrations did not appear to be related to urban traffic. Concentrations of O₃ showed an increasing tendency.

We determined decennial statistical time trends and diurnal statistical patterns of atmospheric particle number concentrations in various relevant size fractions in the city centre of Budapest in an interval of 2008–2018. The mean overall decrease rate of particles in different size fractions was approximately −5 % scaled for the 10-year measurement interval. The decline can be interpreted as a consequence of the decreased anthropogenic emissions in the city.