James Weber* and
Helen F. Dacre
Department of Meteorology, University of Reading, Reading, UK. E-mail: j.m.weber@reading.ac.uk
First published on 15th July 2025
The impact of poor air quality (AQ) on public health has long been recognised and considerable efforts have been made to improve it across the UK. The UK has a far reaching AQ monitoring network and this study summarises the evolution of UK AQ over the period 2015–2024, focusing on the pollutants NO2, O3 and PM2.5 and exploring their drivers. Concentrations of NO2 and PM2.5 exhibit robust negative trends across the whole country while concentrations of O3 increase. Comparing 2015–2016 to 2023–2024, the median number of days per year for which DEFRA AQ sites breached the WHO 2021 target decreased from 136 to 40 (−70%) for NO2 and from 60 to 22 (−63%) for PM2.5. This trend was mirrored in other AQ monitoring networks and highlights that, while progress is being made, acceptable levels of AQ are yet to be reached. Over the same period, median O3 exceedances increased from 7 to 14 days per year. Nationwide analysis of diurnal variation in the pollutants and the use of airmass back trajectory clustering and statistical modelling for three locations – Reading, Sheffield and Glasgow – suggests that local traffic plays a dominant role in NO2 pollution, PM2.5 is influenced more by long range transport and O3 increases are being driven in part by decreases in NO2. From an AQ policy perspective, this suggests continued focus on traffic emissions will reduce NO2, (inter)national rather than local efforts are most critical for PM2.5 improvements, and reductions to VOC emissions must accompany NO2 if further O3 increases are to be avoided.
Environmental significanceUK air quality (AQ) analysis is often done on a local (e.g. city-level) scale given the responsibility of local authorities to improve air quality. There is less focus on national level AQ trends, yet these are important because they cover a much greater population and differences across larger areas provide information as to the major sources of pollution (local emissions v. long range transport) and thus which policies will be effective. We find NO2 and PM2.5 concentrations decrease but breaching of AQ targets remains too frequent while O3 increases. NO2 reductions are linked to traffic while comparison of three distant locations suggests PM2.5 is driven more by long range transport, implying national/international, not just local, policies are needed for its reduction. |
Poor AQ is generally defined in terms of the exposure to high concentrations of key pollutants which negatively affect human and/or vegetation health, including nitrogen dioxide (NO2), ozone (O3) and particulate matter smaller than 2.5 μm in diameter (PM2.5).
PM2.5 particles are small enough to reach deep into the lungs, and in some cases, the bloodstream with subsequent transport around the body and deposition in organs. Elevated levels of PM2.5 are associated with a range of chronic health conditions including respiratory and neurological diseases.3,4 Exposure to high concentrations of NO2 and O3 can also lead to serious health problems.5,6
Pollutant concentrations are determined by the balance of sources (local emissions, longer range transport into a region and chemical production in the atmosphere) and sinks (deposition to terrestrial or aqueous surfaces, chemical destruction and dispersion in the atmosphere). While poor AQ ultimately stems from emissions, both anthropogenic (e.g. nitric oxide (NO) from internal combustion) and natural (e.g. desert dust), meteorology also plays a major role. Stagnant, high pressure conditions can lead to the build up of pollutants from local sources. This infamously happened in the 1952 London Smog where subsidence associated with an anticyclone led to the formation of an atmospheric temperature inversion which prevented pollution from being mixed vertically through the atmosphere, effectively trapping pollutants close to their sources at the surface.7 High wind speeds can disperse local pollution, improving AQ but, depending on their origin, can also transport pollution to a region from elsewhere. Precipitation can enhance loss of soluble pollutants while direct sunlight and higher temperatures drive enhanced photochemical O3 production.8
The influence of meteorology means that it needs to be accounted for when assessing AQ. One way to do this is to use statistical techniques to model directly the impact of meteorology on AQ.9 Another approach, adopted here, is to consider multiyear trends since, over such a period of time, most meteorological conditions will have been sampled at a frequency approximately representative of the longer climatology.
The importance of AQ has been enshrined in law in the United Kingdom for nearly 70 years10 with legislation updated since.11,12 Local authorities are required to monitor AQ in their region and develop air quality management areas (AQMA) in localities where government targets are unlikely to be met.13,14 Since action on emissions is the predominant way policy can influence AQ at scale, several local authorities including Birmingham, Sheffield, Bath and London have enacted clean air15 or low emission16,17 zones, typically levying fines on certain vehicles when they enter. This study does not seek to evaluate the effectiveness of such zones; rather we examine nation-wide trends over the last decade.
Satellite observations over 2005–2015 of the UK found reductions in total column NO2 and aerosol optical depth (AOD), a measure of particulate matter abundance, with NO2 reductions largest in populated areas (∼1–2% per year) while reductions in AOD (2.8–3.3% per year) were more spread out.18 Long term (1992–2019) reductions in NOx = (NO + NO2) have also been recorded at urban and rural surface sites.19–21 Particulate matter concentrations have also declined over the last 30 years.22 However, the difference in concentration between roadside and urban background concentrations is much smaller than that for NO2, likely due to long range transport's larger contribution to particulate matter concentration,23 a topic explored further in this study.
In contrast, O3 has either changed negligibly or increased in recent decades.18 Over the period 1990–2006, surface O3 increased in rural (mean annual trend 0.28 μg m−3 per year) and urban (0.79 μg m−3 per year) sites while NOx concentrations also decreased in urban locations.21 This was attributed to a combination of gradually increasing hemispheric O3, seasonal increases due to regional production via reactions of volatile organic compounds (VOCs) with NOx, and reduced local removal via O3 + NO due to reducing NOx emissions. Diaz et al. (2020) also found consistent long-term increases in mean O3 in rural and urban sites (1992–2019). However, maximum values of O3, which typically occurred in May, exhibited decreases.
This study builds on prior work by documenting the change in the concentration of NO2, O3 and PM2.5 over the last 10 years at more than 500 sites around the UK, compares UK trends to those in continental Europe, relates these concentrations changes to the changes in the frequency with which AQ targets are breached, and decomposes pollutant concentrations by hour of day, day of week and location (urban, rural etc.) to determine what drives their spatial and temporal variability.
Finally, three locations, Reading, Sheffield and Glasgow, located geographically in the south, middle and north of the UK respectively, are considered in detail. AQ, meteorological and airmass back trajectory data are used alongside statistical modelling to compare the major of drivers of NO2, O3 and PM2.5 variability across the locations and the implications for effective AQ policy are discussed.
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Fig. 1 Deseasonalised trend over 2015–2024 from AURN sites of (a) NO2, (b) PM2.5 and (c) O3. Only sites with at least 75% coverage of the time period starting in 2015, running to at least 2023, and where trends are significant at the 95% level are included. The number of qualifying locations for each site type is given by small numbers on the right of each subplot and the height of each boxplot is proportional to the number of qualifying sites. Red lines in (c) show the mean annual trend in O3 at the urban (1993–2006) and rural (1990–2006) sites considered in Jenkin (2008).24 |
Of the 199 qualifying sites for PM2.5 (72 AURN, 127 other), all but 10 exhibited decreasing trends in concentration (median decadal change −30% for AURN) (Fig. 1, S1, S2, S7 and S8†), also largely in line with the European wide decrease (Fig. 2). An obvious feature of both the absolute (Fig. 1 and S1†) and fractional (Fig. S2†) trend plots is that there is not a clear correlation between the trends in NO2 and PM2.5 (R2 = 0.06 for absolute trends). In other words, a site with a large reduction in NO2 does not necessarily have a large reduction in PM2.5. If the sites with the largest NO2 reductions also exhibited the largest PM2.5 reductions, it could be inferred that the pollutants were largely coming from the same source but, as this is not the case, Fig. 1 presents strong evidence that PM2.5 and NO2 are driven by different factors, a finding in line with prior work23 and subject of further discussion in Section 3.4.1.
In contrast to the decreasing concentrations of NO2 and PM2.5, O3 concentrations exhibited increases in 115 of the 121 sites considered (56 AURN, 65 other) (Fig. 1, S7 and S9†) with a median decadal increase of 17% at AURN sites. This increase is in line with positive trends exhibited over much of Northern Europe over the last 10 years (Fig. 2) and qualitatively in agreement with prior UK-focused studies.19,21
Pollutant | Sites | 2015–2016 | 2023–2024 |
---|---|---|---|
NO2 (AURN) | 68 | 136 [82, 230] | 40 [22, 75] |
NO2 (other) | 145 | 225 [172, 308] | 88 [50, 162] |
PM2.5 (AURN) | 40 | 60 [46, 70] | 22 [20, 30] |
PM2.5 (other) | 18 | 47 [27, 56] | 15 [8, 26] |
O3 (AURN) | 53 | 7 [5, 10] | 14 [9, 16] |
O3 (other) | 25 | 6 [2, 7] | 9 [6, 12] |
In line with the increasing O3 concentrations, the number of exceedances of WHO 2021 daily maximum 8-hour average (MDA8) O3 target25 increased from 2015–2016 to 2023–2024 (Table 1, Fig. 3, S10 and S17†). We note this is the opposite finding to Diaz et al. (2020),19 possibly because they used a different AQ target (number of hours per year for which O3 exceeded 50 ppbv ≈ 100 μg m−3). However, the median number of MDA8 exceedances is lower than for NO2 or PM2.5 (Table 1) although this may change if NO2 or PM2.5 continue to decrease, suggesting the focus on AQ policies may need to shift to place greater consideration on O3 in coming decades.
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Fig. 4 Change in mean number of exceedances between 2015–2016 and 2023–2024 for AURN sites with measurements of both NO2 and MDA8 O3. Criteria for calculating exceedance is the same as in Fig. 3. |
If NO2 continues to decrease, more regions may move into a NOx-limited regime where reductions to NOx will drive O3 decreases (a “win–win” for AQ). However, changes to anthropogenic VOC/CO emissions and rising temperatures (which tend to lead to elevated O3 (ref. 26)), may distort this and lead to, in the short term at least, enhanced O3 sensitivity to further NO2 reductions.
NO2 concentrations show pronounced increases in the morning and late afternoon/early evening during the week, particularly at urban traffic sites and, to a lesser extent, urban background sites (Fig. 5). Weekend profiles exhibit a much smaller or even non-existent morning peak and the evening peak typically occurs slightly later than during the week. The contrast between urban week and weekend profiles and the much lower concentrations observed in rural sites points to local traffic emissions as the major driver of NO2. As in Fig. 1 and 2, NO2 concentrations show clear reductions year-on-year to the extent that NO2 at urban traffic sites on weekdays in 2023 and 2024 was lower than in 2020, despite the significant reductions in traffic in 2020 during COVID19 lockdowns.27
By contrast, O3 concentrations show year-on-year increases and are higher at rural than urban sites. Concentrations reach a minimum at urban background sites around 6–7 am GMT, coinciding with the start of the morning rush hour and reduced sunlight. This minimum is more pronounced on weekdays than at the weekend, pointing towards suppression of O3 by NOx from traffic as a driver. Peak O3 concentrations occur in the early afternoon (∼2 pm). As tropospheric O3 has a lifetime of ∼20–30 days (c.f. NO2's lifetime of ∼hours), the diurnal cycle in O3 concentrations is driven by the entrainment of O3 from the free troposphere into the growing boundary layer and deposition to the surface at night, rather than local diurnal O3 production. This entrainment of free tropospheric air complicates the attribution of the drivers of the year-on-year increase in surface O3 by adding another O3 source.
Quantifying the relative importance of local and entrained O3 is challenging, particularly as O3 from northern continental Europe (which will contribute to the entrained free tropospheric O3 experienced in the UK) is also increasing (Fig. 2). Nevertheless, several factors point to reduction in local NO2 (and decrease in NOx-driven suppression) in being influential and thus worthy of policymakers' attention. For example, for all site types, O3 is higher at the weekend than on weekdays, despite both experiencing free tropospheric O3 of similar concentrations, suggesting this difference is driven more by a reduction in NOx-driven suppression. The elevated O3 at rural sites compared to urban sites, the morning rush hour weekday minimum and the anomalously high concentrations in 2020 also support this and provide further evidence that, at the very least, most urban sites in the UK are in VOC-limited regimes, in agreement with prior studies.9 UK wide anthropogenic emissions of CO are predicted to have decreased by 13.4% between 2015 and 2024 (ref. 28) (Fig. S20†) and surface concentrations of CO are decreasing (albeit over a much more limited sensor network, Fig. S21†). However, emissions of NMVOCs, which can produce more O3 per molecule than CO can when they react in the atmosphere, have decreased by less than 1% over that time and both CO and NMVOC emission reductions are outstripped by the 20% decrease in NOx emissions. The response of O3 here suggests that the ongoing efforts to reduce NO2 must be accompanied by enhanced efforts to reduce anthropogenic VOC and CO emissions if further increases in O3 are to be avoided. Rising UK temperatures29,30 and proposals to increase forest cover31 will likely increase UK biogenic VOCs emissions. These have been lower than anthropogenic VOC emissions over the last two decades (by a factor varying between ∼2.5 and ∼10 intra-annually over 2015–2020) (Fig. S22†) but future increases will fuel O3 production. This compounds the importance of reducing anthropogenic VOC emissions still further.
PM2.5 diurnal variations in urban areas also exhibit morning rush hour peaks but, in contrast to NO2, the evening peak tends to see higher concentrations and also occur later (∼7–8 pm GMT vs. 4–5 pm GMT for NO2 in weekday urban traffic sites) suggesting a possible greater contribution from domestic heating, the impact of a shallower nighttime boundary layer and lower sensitivity to local emissions. Furthermore, there is also less of a difference between urban traffic and urban background concentrations and between weekday and weekend profiles. All this points to traffic being a relatively less important source of PM2.5 than NO2, aligning with the trend analysis in Fig. 1.
These trends in NO2, O3 and PM2.5 are also seen when the year-on-year evolution of the seasonal cycles from AURN sites are examined (Fig S23†). NO2 exhibits the highest concentrations in winter months, in line with shallower boundary layers trapping local emissions closer to the surface, but also a clear year-on-year on decrease. Conversely, O3 peaks in April/May, in part due to elevated temperatures promoting deeper boundary layers and free tropospheric air entrainment, and increased consistently over the last decade. PM2.5 exhibits a more muted seasonal cycle, likely due to the greater role of long-range transport which can occur throughout the year, but steady decreases over the period.
The extent to which NO2 and PM2.5 concentrations may continue to change is not the main focus of this study, but some tentative predictions may be derived from Fig. 5 and the year-on-year difference plots (Fig. S24–S26†). Aside from the anomalous result of 2020, urban NO2 concentrations exhibit consistent year-on-year decreases; indeed the 2023 to 2024 decrease was larger than that between 2022 and 2023. This would suggest that a “plateauing” of NO2 concentrations has not yet been reached (i.e. ongoing trends such as the replacement of older vehicles in the fleet with newer, cleaner ones will deliver continued NO2 concentration reductions¶) but this can only be confirmed by further monitoring in real time and accurate modelling. PM2.5 presents a more complex picture – the decrease from 2022 to 2023 was greater than that between 2023 and 2024 – and this is likely in part to be due to the more complex array of sources and enhanced dependence on long range transport (see Section 3.4.1). Meanwhile, future trends in O3, as previously discussed, are likely to be positive as NOx is reduced in chemical regimes where NOx suppresses O3 (although, as previously mentioned, it is possible some regions will eventually tip into NOx-limited regimes where further NOx reductions will reduce O3).
NO2 (Fig. 6D–F) exhibits the highest concentrations in winter months, likely due in part to shallower atmospheric boundary layers reducing pollution transport away from the surface, and the diurnal variation of Fig. 5 is also visible. While airmasses coming from the Atlantic are associated with lower NO2 (C1–C4), no one cluster is associated with much higher concentrations. By contrast, PM2.5 is highest in each location when the air has come from the south-east/European continent (C7 for Reading and Sheffield, C8 for Glasgow).
O3 exhibits maximum concentrations in the mid to late afternoon in the summer months, the period with highest temperatures and boundary layer height. Airmasses coming from northwest Europe are associated with the highest probability of O3 exceeding AQ targets, followed by southerly airmasses.
The similarity in the PM2.5 dependence on airmass origin for the three locations points towards long range transport as the dominant driver. Airmasses from the southeast are likely to contain a mixture of anthropogenic pollution (including from agriculture) from continental Europe and southern England (particularly for Sheffield and Glasgow) as well as Saharan dust on some occasions. This finding is broadly in line with prior modelling studies.32–34
This dependence is also reflected, to some extent, when the variation of exceedance probability with cluster is examined (Fig. 5O and P). The probability of PM2.5 breaching the WHO AQ 2021 target is more than 15% only when the airmass originates from the South or East for Reading (C7, C8), Sheffield (C7, C8), and Glasgow (C6, C7). By contrast, the probability of NO2 exceedance in Reading is high for several “clean” air masses origins as well as C7 and C8.
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Fig. 7 Influence of explanatory variables and trend used by the deweather package when building statistical models of NO2, PM2.5 and O3 for Reading, Sheffield and Glasgow. Variable “hour” refers to hour of day, “weekday” to day of week, “week” to week of year, “wd” to wind direction, “ws” to wind speed and “cluster_int” refers to the air mass back trajectory clusters in Fig. 6. Full PDs shown in Fig. S27–S29.† |
All locations are consistent in having the airmass origin as the most important explanatory variable for PM2.5. Wind speed is the second most influential explanatory variable in each location with low speeds associated with high PM2.5. Such conditions are conducive to the build up of PM2.5 from local emissions and anticyclones over northern Europe whose easterlies along the south side drive long range transport of PM2.5 from the continent.34 All locations exhibit a negative trend, suggesting emissions, local and further afield, are decreasing.
For NO2, air temperature and wind speed are the most important explanatory variables. Increasing wind speed and temperature, conditions associated with enhanced turbulence with a deeper boundary layer and thus dispersion of pollution away from the surface, lead to lower modelled NO2. NO2 also displays a much greater dependence on hour of day than O3 or PM2.5 in all locations, in line with Fig. 5 while airmass origin (i.e. long range transport) accounts for less than 3% of the variability in NO2.
O3 is also influenced substantially by temperature and wind speed but in the opposite way to NO2. Modelled O3 increases with temperature and wind speed, indicative of enhanced production of O3 and mixing of O3-rich free tropospheric air into the boundary layer. Airmass origin is less important for O3 when all hours are considered (accounting for 3–6% of variability), but more influential in the context of exceedance probability (Fig. 6O and P), particularly in Reading. When combined with the UK-wide analysis in Section 3.3, this suggests that while year-on-year increases are being driven by NOx reductions, O3-rich continental air can contribute to elevating concentrations to the point where they breach AQ targets. Since free tropospheric O3 is largely beyond the influence of local authorities, these findings highlight of the importance of local and regional efforts to reduce O3 production by careful management of its precursor emissions: NOx and VOCs/CO.
In contrast to improvements in NO2 and PM2.5, O3 pollution is worsening, likely due to local reductions in NO2. While the benefits of reductions to NO2 have hitherto outweighed the hazards posed by elevated O3 (in terms of changes to frequency with which the WHO AQ targets are breached), this may not always be the case, particularly in a warming world where NO2 is cut further. Effective policy at local scale is possible but this should not target NO2 in isolation: simultaneous reductions in VOCs/CO must also be pursued to temper O3 increases.
One area not explored in this study is compositional analysis of PM2.5. While there are far fewer sites which can conduct this measurement compared to those which measure PM2.5 concentrations, compositional analysis provides substantial information as to the origin of the particulate matter (and its toxicity37) and can thus inform effective mitigation.
Finally, this study, along with the vast majority of literature, focuses on outdoor AQ whereas most humans spend the majority of their lives inside. Indoor pollutant levels differ from those outdoors38 and refining the understanding of the causes and thus possible mitigatory actions of poor indoor AQ, alongside outdoor AQ, should be viewed as a priority.
Footnotes |
† Electronic supplementary information (ESI) available. See DOI: https://doi.org/10.1039/d5ea00055f |
‡ Minimum 75% data coverage, from 2015 to at least 2023, trend statistically significant at 95% confidence level. |
§ Various tests were performed to explore the implications of different types of averaging (i.e. the mean of the means, median of the medians, median of the means, etc.) but no substantive difference to the final result were found. |
¶ This is neither an endorsement nor criticism of clean air/low emission zones. |
This journal is © The Royal Society of Chemistry 2025 |