Effects of Evaporative Emissions Control Measurements on Ozone Concentrations in Brazil

In this work, the possible benefits obtained due to the implementation of evaporative emissions control measures, originating from vehicle fueling processes, on ozone concentrations are verified. The measures studied are: (1) control at the moment when the tank trucks supply the fuel to the gas stations (Stage 1); (2) control at the moment when the vehicles are refueled at the gas stations, through a device installed in the pumps (Stage 2); (3) same as the previous control, but through a device installed in the vehicles (ORVR). The effects of these procedures were analyzed using numerical modeling with the VEIN and WRF/Chem models for a base case in 2018 and different emission scenarios, both in 2018 and 2031. The results obtained for 2018 show that the implementation of Stages 1 and 2 would reduce HCNM emissions by 47.96%, with a consequent reduction of 19.9% in the average concentrations of tropospheric ozone. For 2031, the greatest reductions in ozone concentrations were obtained with the scenario without ORVR, and with Stage 1 and Stage 2 (64.65% reduction in HCNM emissions and 31.93% in ozone), followed by the scenario with ORVR and with Stage 1 and Stage 2 (64.39% reduction in HCNM emissions and 32.98% in ozone concentrations).

Long-Term Trend of Polycyclic Aromatic 1 Hydrocarbon (PAH) Concentrations in Tokyo from 2007 to 2016: Effects of Changes in PAH Emissions and Degradation.

The concentrations of polycyclic aromatic hydrocarbons (PAHs) in aerosol were measured in Shinjuku, which is central Tokyo, Japan, for 10 years from 2007 to 2016. The effects of changes in emission sources and their degradation by reaction with ozone were assessed in this study. There was no significant increasing or decreasing trend of the PAH concentrations during 10 years (P > 0.05). The average selected seven the PAH concentrations (0.88 ng m−3) during 10 years was lower than those in New York and Paris. However, the trend of ozone concentrations is increasing in central Tokyo. This inconsistency raises a question. Did the fact that the ozone concentration was higher than the PAH concentrations promote PAH degradation? To apportion the PAH sources, we used PAH concentration profiles and positive matrix factorization analysis. The contribution of vehicle emissions to the PAHs ranged from 40 to 80 %. Ozone concentrations increased by 3.70 %/year during 10 years. The theoretical degradation rates of PAHs by ozone, which were calculated using a pseudo-first-order rate equation, suggested that the lifetimes of benzo[a]pyrene (BaP) decreased by 1 min from 2007 to 2016. We investigated the aging of BaP using the profile of the isomer ratios. We found that the aging of BaP at the urban and roadside sites were nearly identical indicating aging regardless of the season. Although the decomposition of BaP is promoted by the photochemical oxidation reaction, this result suggests that a certain threshold value exists as the degree of the decomposition. This degradation of PAH can improve chemical loss processes in air quality model.

Exploring the Change in PM2.5 and Ozone Concentrations Caused by Aerosol–Radiation Interactions and Aerosol–Cloud Interactions and the Relationship with Meteorological Factors

Aerosols can interact with other meteorological variables in the air via aerosol–radiation or aerosol–cloud interactions (ARIs/ACIs), thus affecting the concentrations of particle pollutants and ozone. The online-coupled model WRF-Chem was applied to simulate the changes in the PM2.5 (particulate matter less than 2.5 μm in aerodynamic diameter) and ozone concentrations that are caused by these mechanisms in China by conducting three parallel sensitivity tests. In each case, availabilities of aerosol–radiation interactions and aerosol–cloud interactions were set differently in order to distinguish each pathway. Partial correlation coefficients were also analyzed using statistical tools. As suggested by the results, the ARIs reduced ground air temperature, wind speed, and planetary boundary height while increasing relative humidity in most places. Consequently, the ozone concentration in the corresponding region declined by 4%, with a rise in the local annual mean PM2.5 concentration by approximately 12 μm/m3. The positive feedback of the PM2.5 concentration via ACIs was also found in some city clusters across China, despite the overall enhancement value via ACIs being merely around a quarter to half that via ARIs. The change in ozone concentration via ACIs exhibited different trends. The ozone concentration level increased via ACIs, which can be attributed to the drier air in the south and the diminished solar radiation that is received in central and northern China. The correlation coefficient suggests that the suppression in the planetary boundary layer is the most significant factor for the increase in PM2.5 followed by the rise in moisture required for hygroscopic growth. Ozone showed a significant correlation with NO2, while oxidation rates and radiation variance were also shown to be vitally important.

Analysis of Ozone Concentrations between 2002–2020 in Urban Air in Northern Spain

This paper analyses surface ozone measurements at five stations in an urban area (Valladolid) in the upper Spanish plateau over the period 2002–2020. Temporal evolutions, the relationship between ozone and other pollutants such as nitrogen oxides, and the assessment of the ozone concentration trend during the study period were analysed. Daily evolution of ozone at all the stations showed mean maximum concentrations in the afternoon, 15:00 GMT, with values ranging between 73.8 and 80.9 µg m−3, evidencing the influence of photochemical processes favoured by solar radiation in ozone formation. The lowest levels were recorded at night and in the early morning, 7:00 GMT, and were between 23.4 and 32.3 µg m−3, related with the reduction by NO reactions and deposition processes. A broad spring–summer peak between May and July was seen, with the highest values in the latter, with a mean value of up to 73.8 µg m−3. The variation in the monthly mean ozone concentrations of the different percentiles was analysed using a harmonic model. The empirical equation described the experimental values satisfactorily, with a confidence level of 95% and coefficients of determination above 80%, confirming the major decreasing trend in the ozone peak values over the study period.

2020 COVID-19 lockdown and the impacts on air quality with emphasis on urban, suburban and rural zones

Air quality improvements pollution changes due to COVID-19 restrictions have been reported for many urban developments and large metropolitan areas, but the respective impacts at rural and remote zones are less frequently analysed. This study evaluated air pollution changes across all Portugal (68 stations) considering all urban, suburban and rural zones. PM10, PM2.5, NO2, SO2, ozone was analysed in pre-, during, and post-lockdown period (January–May 2020) and for a comparison also in 2019. NO2 was the most reduced pollutant in 2020, which coincided with decreased traffic. Significant drop (15–71%) of traffic related NO2 was observed specifically during lockdown period, being 55% for the largest and most populated region in country. PM was affected to a lesser degree (with substantial differences found for largely populated areas (Lisbon region ~ 30%; North region, up to 49%); during lockdown traffic-related PM dropped 10–70%. PM10 daily limit was exceeded 50% less in 2020, with 80% of exceedances before lockdown period. SO2 decreased by 35%, due to suspended industrial productions, whereas ozone concentrations slightly (though not significantly) increased (83 vs. 80 µg m–3).

Identifying the spatiotemporal variations in ozone formation regimes across China from 2005 to 2019 based on polynomial simulation and causality analysis

Ozone formation regimes are closely related to the ratio of volatile organic compounds (VOCs) to NOx. Different ranges of HCHO/NO2 indicate three formation regimes, including VOC-limited, transitional, and NOx-limited regimes. Due to the unstable interactions between a diversity of precursors, the range of the transitional regime, which plays a key role in identifying ozone formation regimes, remains unclear. To overcome the uncertainties from single models and the lack of reference data, we employed two models, polynomial simulation and convergent cross-mapping (CCM), to identify the ranges of HCHO/NO2 across China based on ground observations and remote sensing datasets. The ranges of the transitional regime estimated by polynomial simulation and CCM were [1.0, 1.9] and [1.0, 1.8]. Since 2013, the ozone formation regime has changed to the transitional and NOx-limited regime all over China, indicating that ozone concentrations across China were mainly controlled by NOx. However, despite the NO2 concentrations, HCHO concentrations continuously exert a positive influence on ozone concentrations under transitional and NOx-limited regimes. Under the circumstance of national NOx reduction policies, the increase in VOCs became the major driver for the soaring ozone pollution across China. For an effective management of ozone pollution across China, the emission reduction in VOCs and NOx should be equally considered.