Ozone Enhancement Research Articles

Stratospheric ozone intrusion events and their impacts on tropospheric ozone in the Southern Hemisphere

Abstract. Stratosphere-to-troposphere transport (STT) provides an important natural source of ozone to the upper troposphere, but the characteristics of STT events in the Southern Hemisphere extratropics and their contribution to the regional tropospheric ozone budget remain poorly constrained. Here, we develop a quantitative method to identify STT events from ozonesonde profiles. Using this method we estimate the seasonality of STT events and quantify the ozone transported across the tropopause over Davis (69° S, 2006–2013), Macquarie Island (54° S, 2004–2013), and Melbourne (38° S, 2004–2013). STT seasonality is determined by two distinct methods: a Fourier bandpass filter of the vertical ozone profile and an analysis of the Brunt–Väisälä frequency. Using a bandpass filter on 7–9 years of ozone profiles from each site provides clear detection of STT events, with maximum occurrences during summer and minimum during winter for all three sites. The majority of tropospheric ozone enhancements owing to STT events occur within 2.5 and 3 km of the tropopause at Davis and Macquarie Island respectively. Events are more spread out at Melbourne, occurring frequently up to 6 km from the tropopause. The mean fraction of total tropospheric ozone attributed to STT during STT events is ∼ 1. 0–3. 5 % at each site; however, during individual events, over 10 % of tropospheric ozone may be directly transported from the stratosphere. The cause of STTs is determined to be largely due to synoptic low-pressure frontal systems, determined using coincident ERA-Interim reanalysis meteorological data. Ozone enhancements can also be caused by biomass burning plumes transported from Africa and South America, which are apparent during austral winter and spring and are determined using satellite measurements of CO. To provide regional context for the ozonesonde observations, we use the GEOS-Chem chemical transport model, which is too coarsely resolved to distinguish STT events but is able to accurately simulate the seasonal cycle of tropospheric ozone columns over the three southern hemispheric sites. Combining the ozonesonde-derived STT event characteristics with the simulated tropospheric ozone columns from GEOS-Chem, we estimate STT ozone flux near the three sites and see austral summer dominated yearly amounts of between 5. 7 and 8. 7 × 1017 molecules cm−2 a−1.

Unusual enhancement in tropospheric and surface ozone due to orography induced gravity waves

In this study, we investigate the causative processes responsible for the observed enhancement in the tropospheric and surface ozone during December 09–11, 2008 orography induced gravity wave event over Himalayan region. The analysis is done using surface ozone measurements and satellite datasets from Atmospheric Infrared Sounder/Advanced Microwave Sounding Unit-A (AIRS/AMSU-A), COSMIC, TES and Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO). Observations depict a two fold increase in surface and tropospheric ozone during the event as compared to normal days in both AIRS and TES ozone measurements. COSMIC temperature perturbations show generation of shorter vertical wavelengths efficient for the sub-tropical tropopause folding due to orography induced gravity waves. Moreover, the intense tropopause folding as evidenced by upward-downward vertical velocities couplet could trigger the intrusion of stratospheric ozone rich air into upper tropospheric ozone poor air as also confirmed by high values of potential vorticity during the observational period. Hence, present study reemphasizes the importance of wave induced atmospheric dynamics on atmospheric constituents' especially tropospheric ozone over Himalayan region.

Comparison of ultraviolet absorbance and NO-chemiluminescence for ozone measurement in wildfire plumes at the Mount Bachelor Observatory

The goal of this paper is to evaluate the accuracy of the commonly used ozone (O3) instrument (the ultraviolet (UV) photometer) against a Federal Reference Method (Nitric Oxide –chemiluminescence) for ozone measurement in wildfire smoke plumes. We carried out simultaneous ozone measurement with two UV O3 photometers and one nitric oxide–chemiluminescence (NO-CL) ozone detectors during wildfire season (Aug. 1–Sept. 30) in 2015 at the Mount Bachelor Observatory (MBO, 2763 m above mean sea level, Oregon, USA). The UV O3 shows good agreement and excellent correlation to NO-CL O3, with linear regression slopes close to unity and R2 of 0.92 for 1-h average data and R2 of 0.93 for O3 daily maximum 8-h average (MDA8). During this two-month period we identified 35 wildfire events. Ozone enhancements in those wildfire plumes measured by NO-CL O3 and UV O3 monitors also show good agreement and excellent linear correlation, with a slope and R2 of 1.03 and 0.86 for O3 enhancements (ΔO3) and 1.00 and 0.98 for carbon monoxide (CO)-normalized ozone enhancement ratios (ΔO3/ΔCO), respectively. Overall, the UV O3 was found to have a positive bias of 4.7 ± 2.8 ppbv compared to the NO-CL O3. The O3 bias between NO-CL O3 and UV O3 is independent of wildfire plume tracers such as CO, particulate matter (PM1), aerosol scattering, and ultrafine particles. The results demonstrate that the UV O3 absorbance method is reliable, even in highly concentrated wildfire plumes.

Mitigating the Climate Impact from Aviation: Achievements and Results of the DLR WeCare Project

The WeCare project (Utilizing Weather information for Climate efficient and eco efficient future aviation), an internal project of the German Aerospace Center (Deutsches Zentrum für Luft- und Raumfahrt, DLR), aimed at finding solutions for reducing the climate impact of aviation based on an improved understanding of the atmospheric impact from aviation by making use of measurements and modeling approaches. WeCare made some important contributions to advance the scientific understanding in the area of atmospheric and air transportation research. We characterize contrail properties, show that the aircraft type significantly influences these properties, and how contrail-cirrus interacts with natural cirrus. Aviation NOx emissions lead to ozone formation and we show that the strength of the ozone enhancement varies, depending on where within a weather pattern NOx is emitted. These results, in combination with results on the effects of aerosol emissions on low cloud properties, give a revised view on the total radiative forcing of aviation. The assessment of a fleet of strut-braced wing aircraft with an open rotor is investigated and reveals the potential to significantly reduce the climate impact. Intermediate stop operations have the potential to significantly reduce fuel consumption. However, we find that, if only optimized for fuel use, they will have an increased climate impact, since non-CO2 effects compensate the reduced warming from CO2 savings. Avoiding climate sensitive regions has a large potential in reducing climate impact at relatively low costs. Taking advantage of a full 3D optimization has a much better eco-efficiency than lateral re-routings, only. The implementation of such operational measures requires many more considerations. Non-CO2 aviation effects are not considered in international agreements. We showed that climate-optimal routing could be achieved, if market-based measures were in place, which include these non-CO2 effects. An alternative measure to foster climate-optimal routing is the closing of air spaces, which are very climate-sensitive. Although less effective than an unconstrained optimization with respect to climate, it still has a significant potential to reduce the climate impact of aviation. By combining atmospheric and air transportation research, we assess climate mitigation measures, aiming at providing information to aviation stakeholders and policy-makers to make aviation more climate compatible.

Influence of the North American monsoon on Southern California tropospheric ozone levels during summer in 2013 and 2014

AbstractThe impact of the North American (NA) monsoon on tropospheric ozone variability in Southern California is investigated using lidar measurements at Jet Propulsion Laboratory‐Table Mountain Facility, California, and the chemical‐transport model GEOS‐Chem. Routine lidar observations obtained in July–August 2013–2014 reveal a consistent ozone enhancement of 23 ppbv in the free troposphere (6–9 km), when ozone‐rich air is transported along the western edge of the upper level anticyclone associated with the NA monsoon from regions where maximum lightning‐induced NOx production occurs. When the high‐pressure system shifts to the southeast, a zonal westerly flow of the air parcels reaching the Table Mountain Facility (TMF) occurs, prohibiting the lightning‐induced ozone enhanced air to reach TMF. This modulation of tropospheric ozone by the position of the NA monsoon anticyclone could have implications on long‐term ozone trends associated with our changing climate, due to the expected widening of the tropical belt affecting the strength and position of the anticyclone.

Enhanced surface ozone during the heat wave of 2013 in Yangtze River Delta region, China

Under the background of global warming, occurrence of heat waves has increased in most part of Europe, Asia and Australia along with enhanced ozone level. In this paper, observational air temperature and surface ozone in the Yangtze River Delta (YRD) region of China during summer of 2013, and the regional chemistry-climate model (RegCM-CHEM4) were applied to explore the relationship between heat wave and elevated ground-level ozone. Observations indicated that YRD experienced severe heat waves with maximum temperature up to 41.1°C, 6.1°C higher than the definition of heat wave in China, and can last for as long as 27days. Maximum ozone reached 160.5ppb, exceeding the national air quality standard (secondary level) as 74.7ppb. Moreover, ozone was found to increase at a rate of 4–5ppbK−1 within the temperature range of 28–38°C, but decrease by a rate of −1.3~−1.7ppbK−1 under extremely high temperature. A typical heat wave case (HW: 24/7–31/7) and non-heat wave case (NHW: 5/6–12/6) were selected to investigate the mechanism between heavy ozone and heat waves. It was found that chemical reactions play the most important role in ozone formation during HW days, which result in 12ppb ozone enhancement compared to NHW days. Chemical formation of ozone can be influenced by several factors. During heat waves, a more stagnant condition, controlled by anti-cyclone with sink airflow, led to less water vapor in YRD from south and contributed to less cloud cover, which favored a strong solar radiation environment and ozone significantly increasing. High temperature also slightly promote the effect of vertical turbulence and horizontal advection, which beneficial to ozone remove, but the magnitude is much smaller than chemical effect. Our study suggests that the chemical reaction will potentially lead to substantial elevated ozone in a warmer climate, which should be taken into account in future ozone related issues.

Tropospheric ozone maxima observed over the Arabian Sea during the pre-monsoon

Abstract. An enhancement of the tropospheric ozone column (TOC) over Arabian Sea (AS) during the pre-monsoon season is reported in this study. The potential sources of the AS spring ozone pool are investigated by use of multiple data sets (e.g., SCIAMACHY Limb-Nadir-Matching TOC, OMI/MLS TOC, TES TOC, MACC reanalysis data, MOZART-4 model and HYSPLIT model). Three-quarters of the enhanced ozone concentrations are attributed to the 0–8 km height range. The main source of the ozone enhancement is considered to be caused by long-range transport of ozone pollutants from India (∼ 50 % contributions to the lowest 4 km, ∼ 20 % contributions to the 4–8 km height range), the Middle East, Africa and Europe (∼ 30 % in total). In addition, the vertical pollution accumulation in the lower troposphere, especially at 4–8 km, was found to be important for the AS spring ozone pool formation. Local photochemistry, on the other hand, plays a negligible role in producing ozone at the 4–8 km height range. In the 0–4 km height range, ozone is quickly removed by wet deposition. The AS spring TOC maxima are influenced by the dynamical variations caused by the sea surface temperature (SST) anomaly during the El Niño period in 2005 and 2010 with a ∼ 5 DU decrease.

Ozone production by corona discharges during a convective event in DISCOVER-AQ Houston

An ozonesonde launched near electrically active convection in Houston, TX on 5 September 2013 during the NASA DISCOVER-AQ project measured a large enhancement of ozone throughout the troposphere. A separate ozonesonde was launched from Smith Point, TX (∼58 km southeast of the Houston site) at approximately the same time as the launch from Houston and did not measure that enhancement. Furthermore, ozone profiles for the descent of both sondes agreed well with the ascending Smith Point profile, suggesting a highly localized event in both space and time in which an anomalously large enhancement of 70–100 ppbv appeared in the ascending Houston ozonesonde data. Compared to literature values, such an enhancement appears to be the largest observed to date. Potential sources of the localized ozone enhancement such as entrainment of urban or biomass burning emissions, downward transport from the stratosphere, photochemical production from lightning NOx, and direct ozone production from corona discharges were investigated using model simulations. We conclude that the most likely explanation for the large ozone enhancement is direct ozone production by corona discharges. Integrating the enhancement seen in the Houston ozone profile and using the number of electrical discharges detected by the NLDN (or HLMA), we estimate a production of 2.48 × 1028 molecules of ozone per flash which falls within the range of previously recorded values (9.89 × 1026–9.82 × 1028 molecules of ozone per flash). Since there is currently no parameterization for the direct production of ozone from corona discharges we propose the implementation of an equation into a chemical transport model. Ultimately, additional work is needed to further understand the occurrence and impact of corona discharges on tropospheric chemistry on short and long timescales.

Biomass burning and biogenic aerosols in northern Australia during the SAFIRED campaign

Abstract. There is a lack of knowledge of how biomass burning aerosols in the tropics age, including those in the fire-prone Northern Territory in Australia. This paper reports chemical characterization of fresh and aged aerosols monitored during the 1-month-long SAFIRED (Savannah Fires in the Early Dry Season) field study, with an emphasis on the chemical signature and aging of organic aerosols. The campaign took place in June 2014 during the early dry season when the surface measurement site, the Australian Tropical Atmospheric Research Station (ATARS), located in the Northern Territory, was heavily influenced by thousands of wild and prescribed bushfires. ATARS was equipped with a wide suite of instrumentation for gaseous and aerosol characterization. A compact time-of-flight aerosol mass spectrometer was deployed to monitor aerosol chemical composition. Approximately 90 % of submicron non-refractory mass was composed of organic material. Ozone enhancement in biomass burning plumes indicated increased air mass photochemistry. The diversity in biomass burning emissions was illustrated through variability in chemical signature (e.g. wide range in f44, from 0.06 to 0.18) for five intense fire events. The background particulate loading was characterized using positive matrix factorization (PMF). A PMF-resolved BBOA (biomass burning organic aerosol) factor comprised 24 % of the submicron non-refractory organic aerosol mass, confirming the significance of fire sources. A dominant PMF factor, OOA (oxygenated organic aerosol), made up 47 % of the sampled aerosol, illustrating the importance of aerosol aging in the Northern Territory. Biogenic isoprene-derived organic aerosol factor was the third significant fraction of the background aerosol (28 %).

An Atlantic streamer in stratospheric ozone observations and SD-WACCM simulation data

Abstract. Observation and simulation of individual ozone streamers are important for the description and understanding of non-linear transport processes in the middle atmosphere. A sudden increase in mid-stratospheric ozone occurred above central Europe on 4 December 2015. The GROund-based Millimeter-wave Ozone Spectrometer (GROMOS) and the Stratospheric Ozone MOnitoring RAdiometer (SOMORA) in Switzerland measured an ozone enhancement of about 30 % at 34 km altitude (8.3 hPa) from 1 to 4 December. A similar ozone increase is simulated by the Specified Dynamics Whole Atmosphere Community Climate (SD-WACCM) model. Further, the global ozone fields at 34 km altitude (8.3 hPa) from SD-WACCM and the satellite experiment Aura/MLS show a remarkable agreement for the location and timing of an ozone streamer (large-scale tongue-like structure) extending from the subtropics in northern America over the Atlantic to central Europe. This agreement indicates that SD-WACCM can inform us about the wind inside the Atlantic ozone streamer. SD-WACCM shows an eastward wind of about 100 m s−1 inside the Atlantic streamer in the mid-stratosphere. SD-WACCM shows that the Atlantic streamer flows along the edge of the polar vortex. The Atlantic streamer turns southward at an erosion region of the polar vortex located above the Caspian Sea. The spatial distribution of stratospheric water vapour indicates a filament outgoing from this erosion region. The Atlantic streamer, the polar vortex erosion region and the water vapour filament belong to the process of planetary wave breaking in the so-called surf zone of the northern midlatitude winter stratosphere.

Convective storms and non-classical low-level jets during high ozone level episodes in the Amazon region: An ARM/GOAMAZON case study

In this work, we investigate the ozone dynamics during the occurrence of both downdrafts associated with mesoscale convective storms and non-classical low-level jets. Extensive data sets, comprised of air chemistry and meteorological observations made in the Amazon region of Brazil over the course of 2014–15, are analyzed to address several questions. A first objective is to investigate the atmospheric thermodynamic and dynamic conditions associated with storm-generated ozone enhancements in the Amazon region. A second objective is to determine the magnitude and the frequency of ground-level ozone enhancements related to low-level jets. Ozone enhancements are analyzed as a function of wind shear, low-level jet maximum wind speed, and altitude of jet core. Strong and sudden increases in ozone levels are associated with simultaneous changes in variables such as horizontal wind speed, convective available potential energy, turbulence intensity and vertical velocity skewness. Rapid increases in vertical velocity skewness give support to the hypothesis that the ozone enhancements are directly related to downdrafts. Low-level jets associated with advancing density currents are often present during and after storm downdrafts that transport ozone-enriched air from aloft to the surface.

Summertime tropospheric ozone enhancement associated with a cold front passage due to stratosphere‐to‐troposphere transport and biomass burning: Simultaneous ground‐based lidar and airborne measurements

AbstractStratosphere‐to‐troposphere transport (STT) and biomass burning (BB) are two important natural sources for tropospheric ozone that can result in elevated ozone and air‐quality episode events. High‐resolution observations of multiple related species are critical for complex ozone source attribution. In this article, we present an analysis of coinciding ground‐based and airborne observations, including ozone lidar, ozonesonde, high spectral resolution lidar (HSRL), and multiple airborne in situ measurements, made on 28 and 29 June 2013 during the Southeast Nexus field campaign. The ozone lidar and HSRL reveal detailed ozone and aerosol structures as well as the temporal evolution associated with a cold front passage. The observations also captured two enhanced (+30 ppbv) ozone layers in the free troposphere (FT), which were determined from this study to be caused by a mixture of BB and stratospheric sources. The mechanism for this STT is tropopause folding associated with a cutoff upper level low‐pressure system according to the analysis of its potential vorticity structure. The depth of the tropopause fold appears to be shallow for this case compared to events observed in other seasons; however, the impact on lower tropospheric ozone was clearly observed. This event suggests that strong STT may occur in the southeast United States during the summer and can potentially impact lower troposphere during these times. Statistical analysis of the airborne observations of trace gases suggests a coincident influence of BB transport in the FT impacting the vertical structure of ozone during this case study.

Hydrological controls on the tropospheric ozone greenhouse gas effect

The influence of the hydrological cycle in the greenhouse gas (GHG) effect of tropospheric ozone (O3) is quantified in terms of the O3 longwave radiative effect (LWRE), which is defined as the net reduction of top-of-atmosphere flux due to total tropospheric O3 absorption. The O3 LWRE derived from the infrared spectral measurements by Aura’s Tropospheric Emission Spectrometer (TES) show that the spatiotemporal variation of LWRE is relevant to relative humidity, surface temperature, and tropospheric O3 column. The zonally averaged subtropical LWRE is ~0.2 W m–2 higher than the zonally averaged tropical LWRE, generally due to lower water vapor concentrations and less cloud coverage at the downward branch of the Hadley cell in the subtropics. The largest values of O3 LWRE over the Middle East (>1 W/m2) are further due to large thermal contrasts and tropospheric ozone enhancements from atmospheric circulation and pollution. Conversely, the low O3 LWRE over the Inter-Tropical Convergence Zone (on average 0.4 W m–2) is due to strong water vapor absorption and cloudiness, both of which reduce the tropospheric O3 absorption in the longwave radiation. These results show that changes in the hydrological cycle due to climate change could affect the magnitude and distribution of ozone radiative forcing.

Tropospheric Ozone Climatology in Eastern Equatorial Africa

Tropospheric ozone climatology in eastern Equatorial Africa has been at the core of this study. Seasonal and annual tropospheric ozone distribution and variation have been investigated using SHADOZ network data from Nairobi for the period 1998-2013. Meteorological parameters including air temperature, relative humidity, atmospheric pressure as well as ozone partial pressure have permitted to provide the first comprehensible tropospheric ozone climatology over this region. Mean seasonal tropospheric ozone distribution displays two distinct peaks occurring in winter with 43 DU (July) and 46.8 DU in spring (October). Comparison of mean seasonal ozone partial pressure with relative humidity profiles shows a logarithmic trend with strong regression coefficient for ozone partial pressure (0.81<R2<0.92). Conversely relative humidity variation displays a linear trend with a weak seasonal regression (0.57<R2<0.74). Seasonal vertical tropospheric ozone variation displays two ozone peaks of 121 ppbv in JJA and 126 ppbv in SON at 100 hPa respectively. A minimum photochemical source contribution from local and neighboring countries has been noted at surface to mid latitude. Investigation of individual profiles chosen as case studies for JJA (25/07/2001) and SON (09/10/2002), to assess the origin of high tropospheric ozone concentration has been performed by using back trajectory HYSPLIT model. The strong role played by the Indian Ocean in the long range transport of easterly air mass into eastern Africa at mid and upper troposphere in both seasons has been confirmed. However mean monthly NCEP/NCAR Reanalysis model used to assess the contribution of STE (Stratospheric Tropospheric Exchange), shows a positive mean eddy divergence values during the months of June to July 2001, with evidence of high vorticity 1 sigma values occurring over the same period. In summer higher positive 1 sigma divergence as well as 1 sigma vorticity values have been noted showing stronger STE activity occurring in SON period. These parameters suggest that STE contribution to ozone enhancement in equatorial east Africa is stronger during SON than in JJA. Given the complexity of climate patterns over the equatorial region, in which Nairobi is located, the influence of ENSO (El Nino-Southern Oscillation) and QBO (Quasi Biennial Oscillation) in the STE occurrence cannot be excluded as noted by previous studies.

On the summertime air quality and related photochemical processes in the megacity Shanghai, China.

Summertime surface ozone (O3) and related secondary formation of fine particles are the major air quality concerns in the megacity of Shanghai. We performed mobile Cavity Enhanced Differential Optical Absorption Spectroscopy (CE-DOAS) measurements to investigate the spatial distribution of on-road nitrogen dioxide (NO2) concentrations along the Inner Ring Elevated Road (IRER) in Shanghai. The observations show a ratio of 4 between CE-DOAS averaged on-road NO2 and the in-situ ambient measurements, illustrating the strong impact of vehicle emissions over the urban area. The air mass transport analysis suggests that the observed episodic ozone events arise from both the abundance of volatile organic compounds (VOCs) precursors in the sampled plume and the regional transport of ozone-rich air masses. Analysis of the sources of PM2.5 shows that the secondary heterogeneous gas-to-particle conversion of sulfate and nitrate from sulfur dioxide (SO2) and nitrogen oxides (NOx) is the largest source of PM2.5 contributing 44.8±9.2% of the total PM2.5. Ozone-related photochemical formation of fine particles is estimated to contribute about 22.5±11.9% of the total PM2.5, which is strongly facilitated by solar radiation in summer. According to our results, nitrous acid (HONO) is the major precursor of hydroxyl radicals (OH) accounting for 40% to 80% of the total OH production during daytime. A significant correlation is found between the HONO levels in the early morning and the daily O3 and PM2.5 levels. The summertime measurements indicate that the photolytic reaction of HONO after sunrise increased the abundance of daytime OH and oxidative capacity, resulting in an enhancement of ground level ozone and secondary organic aerosol formation. This study provides quantitative information to better understand photochemical formation of ozone and fine particles in Shanghai during summertime, which is useful for designing collaborative strategies to mitigate emissions of precursor pollutants.

Wildfire influences on the variability and trend of summer surface ozone in the mountainous western United States

Abstract. Increasing wildfire activities in the mountainous western US may present a challenge for the region to attain a recently revised ozone air quality standard in summer. Using current Eulerian chemical transport models to examine the wildfire ozone influences is difficult due to uncertainties in fire emissions, inadequate model chemistry, and resolution. Here we quantify the wildfire influence on the ozone variability, trends, and number of high MDA8 (daily maximum 8 h average) ozone days over this region in summers (June, July, and August) 1989–2010 using a new approach. We define a fire index using retroplumes (plumes of back-trajectory particles) computed by a Lagrangian dispersion model (FLEXPART) and develop statistical models based on the fire index and meteorological parameters to interpret MDA8 ozone concentrations measured at 13 Intermountain West surface sites. We show that the statistical models are able to capture the ozone enhancements by wildfires and give results with some features different from the GEOS-Chem Eulerian chemical transport model. Wildfires enhance the Intermountain West regional summer mean MDA8 ozone by 0.3–1.5 ppbv (daily episodic enhancements reach 10–20 ppbv at individual sites) with large interannual variability, which are strongly correlated with the total MDA8 ozone. We find large fire impacts on the number of exceedance days; for the 13 CASTNet sites, 31 % of the summer days with MDA8 ozone exceeding 70 ppbv would not occur in the absence of wildfires.

The impact of synoptic weather on UK surface ozone and implications for premature mortality

Air pollutants, such as ozone, have adverse impacts on human health and cause, for example, respiratory and cardiovascular problems. In the United Kingdom (UK), peak surface ozone concentrations typically occur in the spring and summer and are controlled by emission of precursor gases, tropospheric chemistry and local meteorology which can be influenced by large-scale synoptic weather regimes. In this study we composite surface and satellite observations of summer-time (April to September) ozone under different UK atmospheric circulation patterns, as defined by the Lamb weather types. Anticyclonic conditions and easterly flows are shown to significantly enhance ozone concentrations over the UK relative to summer-time average values. Anticyclonic stability and light winds aid the trapping of ozone and its precursor gases near the surface. Easterly flows (NE, E, SE) transport ozone and precursor gases from polluted regions in continental Europe (e.g. the Benelux region) to the UK. Cyclonic conditions and westerly flows, associated with unstable weather, transport ozone from the UK mainland, replacing it with clean maritime (North Atlantic) air masses. Increased cloud cover also likely decrease ozone production rates. We show that the UK Met Office regional air quality model successfully reproduces UK summer-time ozone concentrations and ozone enhancements under anticyclonic and south-easterly conditions for the summer of 2006. By using established ozone exposure-health burden metrics, anticyclonic and easterly condition enhanced surface ozone concentrations pose the greatest public health risk.

Nocturnal surface ozone enhancement over Portugal during winter: Influence of different atmospheric conditions

Four distinct nocturnal surface ozone (NSO) enhancement events were observed, with NSO concentration exceeding 80μg/m3, at multiple ozone (O3) monitoring stations (32 sites) in January, November and December between year 2000–2010, in Portugal. The reasonable explanation for the observed bimodal pattern of surface ozone with enhanced NSO concentration during nighttime has to be transport processes, as the surface ozone production ceases at nighttime. Simultaneous measurements of O3 at multiple stations during the study period in Portugal suggest that horizontal advection alone cannot explain the observed NSO enhancement. Thus, detailed analysis of the atmospheric conditions, simulated with the Weather Research and Forecasting (WRF) model, were performed to evaluate the atmospheric mechanisms responsible for NSO enhancement in the region. Simulations revealed that each event occurred as a result of one or the combination of different atmospheric processes such as, passage of a cold front followed by a subsidence zone; passage of a moving surface trough, with associated strong horizontal wind speed and vertical shear; combination of vertical and horizontal transport at the synoptic scale; formation of a low level jet with associated vertical mixing below the jet stream. The study confirmed that large-scale flow pattern resulting in enhanced vertical mixing in the nocturnal boundary layer, plays a key role in the NSO enhancement events, which frequently occur over Portugal during winter months.

Evaluating Summer-Time Ozone Enhancement Events in the Southeast United States

This study evaluates source attribution of ozone (O3) in the southeast United States (US) within O3 lamina observed by the University of Alabama in Huntsville (UAH) Tropospheric Ozone Lidar Network (TOLNet) system during June 2013. This research applies surface-level and airborne in situ data and chemical transport model simulations (GEOS-Chem) in order to quantify the impact of North American anthropogenic emissions, wildfires, lightning NOx, and long-range/stratospheric transport on the observed O3 lamina. During the summer of 2013, two anomalous O3 layers were observed: (1) a nocturnal near-surface enhancement and (2) a late evening elevated (3–6 km above ground level) O3 lamina. A “brute force” zeroing method was applied to quantify the impact of individual emission sources and transport pathways on the vertical distribution of O3 during the two observed lamina. Results show that the nocturnal O3 enhancement on 12 June 2013 below 3 km was primarily due to wildfire emissions and the fact that daily maximum anthropogenic emission contributions occurred during these night-time hours. During the second case study it was predicted that above average contributions from long-range/stratospheric transport was largely contributing to the O3 lamina observed between 3 and 6 km on 29 June 2013. Other models, remote-sensing observations, and ground-based/airborne in situ data agree with the source attribution predicted by GEOS-Chem simulations. Overall, this study demonstrates the dynamic atmospheric chemistry occurring in the southeast US and displays the various emission sources and transport processes impacting O3 enhancements at different vertical levels of the troposphere.

Impact of emissions and +2 °C climate change upon future ozone and nitrogen dioxide over Europe

The evolution of ozone and nitrogen dioxide over Europe between the present day and a future period with a +2 °C global warming relative to the pre-industrial climate was studied using four offline chemistry transport models, each driven by a different climate model. Given the recent outcome of the COP21 negotiations, understanding the implications of climate change around the +2 °C threshold has never been more pressing or relevant. One of the objectives of this study was to show how changes in anthropogenic emissions and +2 °C climate change are expected to affect future air quality, which may have important implications upon human health. It was found that a +2 °C climate change alone was responsible for a modest, and not statistically significant, increase in surface O3 concentrations (of between −0.1–0.8 ppb in the summer averaged over the European domain) compared to the present climate. Two different emission scenarios were used for the future time period in order to provide an estimate of the extent of air pollution reductions that could occur if (a) all currently planned air quality legislation is implemented and (b) all maximum technologically feasible emission reductions are implemented. The results showed that summer O3 could be reduced by between 4 and 5 ppb under a current legislation scenario, with at least 3 ppb of further reductions under the maximum mitigated scenario. Calculations of summer ozone enhancement were used as a metric to analyse the results after having removed background ozone level changes. In conclusion it was found that future air quality on a regional scale will depend upon the implementation of effective emission reduction policy; the positive effects of which should not be hindered by a +2 °C global warming.