We discuss remote terrestrial influences on boundary layer air over the Southern Ocean and Antarctica, and the mechanisms by which they arise, using atmospheric radon observations as a proxy. Our primary motivation was to enhance the scientific community's ability to understand and quantify the potential effects of pollution, nutrient or pollen transport from distant land masses to these remote, sparsely instrumented regions. Seasonal radon characteristics are discussed at 6 stations (Macquarie Island, King Sejong, Neumayer, Dumont d'Urville, Jang Bogo and Dome Concordia) using 1-4 years of continuous observations. Context is provided for differences observed between these sites by Southern Ocean radon transects between 45 and 67 • S made by the Research Vessel Investigator. Synoptic transport of continental air within the marine boundary layer (MBL) dominated radon seasonal cycles in the mid-Southern Ocean site (Macquarie Island). MBL synoptic transport, tropospheric injection, and Antarctic outflow all contributed to the seasonal cycle at the sub-Antarctic site (King Sejong). Tropospheric subsidence and injection events delivered terrestrially influenced air to the Southern Ocean MBL in the vicinity of the circumpolar trough (or "Polar Front"). Katabatic outflow events from Antarctica were observed to modify trace gas and aerosol characteristics of the MBL 100-200 km off the coast. Radon seasonal cycles at coastal Antarctic sites were dominated by a combination of local radon sources in summer and subsidence of terrestrially influenced tropospheric air, whereas those on the Antarctic Plateau were primarily controlled by tropospheric subsidence. Separate characterization of long-term marine and katabatic flow air masses at Dumont d'Urville revealed monthly mean differences in summer of up to 5 ppbv in ozone and 0.3 ng m −3 in gaseous

Abstract. The Measurements of Urban, Marine and Biogenic Air (MUMBA) campaign took place in Wollongong, New South Wales (a small coastal city approximately 80 km south of Sydney, Australia) from 21 December 2012 to 15 February 2013. Like many Australian cities, Wollongong is surrounded by dense eucalyptus forest, so the urban airshed is heavily influenced by biogenic emissions. Instruments were deployed during MUMBA to measure the gaseous and aerosol composition of the atmosphere with the aim of providing a detailed characterisation of the complex environment of the ocean–forest–urban interface that could be used to test the skill of atmospheric models. The gases measured included ozone, oxides of nitrogen, carbon monoxide, carbon dioxide, methane and many of the most abundant volatile organic compounds. The aerosol characterisation included total particle counts above 3 nm, total cloud condensation nuclei counts, mass concentration, number concentration size distribution, aerosol chemical analyses and elemental analysis.The campaign captured varied meteorological conditions, including two extreme heat events, providing a potentially valuable test for models of future air quality in a warmer climate. There was also an episode when the site sampled clean marine air for many hours, providing a useful additional measure of the background concentrations of these trace gases within this poorly sampled region of the globe. In this paper we describe the campaign, the meteorology and the resulting observations of atmospheric composition in general terms in order to equip the reader with a sufficient understanding of the Wollongong regional influences to use the MUMBA datasets as a case study for testing a chemical transport model. The data are available from PANGAEA (http://doi.pangaea.de/10.1594/PANGAEA.871982).

Accurate air quality modelling is an essential tool, both for strategic assessment (regulation development for emission controls) and for short-term forecasting (enabling warnings to be issued to protect vulnerable members of society when the pollution levels are predicted to be high). Model intercomparison studies are a valuable support to this work, being useful for identifying any issues with air quality models, and benchmarking their performance against international standards, thereby increasing confidence in their predictions. This paper presents the results of a comparison study of six chemical transport models which have been used to simulate short-term hourly to 24 hourly concentrations of fine particulate matter less than and equal to 2.5 µm in diameter (PM2.5) and ozone (O3) for Sydney, Australia. Model performance was evaluated by comparison to air quality measurements made at 16 locations for O3 and 5 locations for PM2.5, during three time periods that coincided with major atmospheric composition measurement campaigns in the region. These major campaigns included daytime measurements of PM2.5 composition, and so model performance for particulate sulfate (SO42−), nitrate (NO3−), ammonium (NH4+) and elemental carbon (EC) was evaluated at one site per modelling period. Domain-wide performance of the models for hourly O3 was good, with models meeting benchmark criteria and reproducing the observed O3 production regime (based on the O3/NOx indicator) at 80% or more of the sites. Nevertheless, model performance was worse at high (and low) O3 percentiles. Domain-wide model performance for 24 h average PM2.5 was more variable, with a general tendency for the models to under-predict PM2.5 concentrations during the summer and over-predict PM2.5 concentrations in the autumn. The modelling intercomparison exercise has led to improvements in the implementation of these models for Sydney and has increased confidence in their skill at reproducing observed atmospheric composition.

This paper presents a summary of the key findings of the special issue of Atmosphere on Air Quality in New South Wales and discusses the implications of the work for policy makers and individuals. This special edition presents new air quality research in Australia undertaken by (or in association with) the Clean Air and Urban Landscapes hub, which is funded by the National Environmental Science Program on behalf of the Australian Government’s Department of the Environment and Energy. Air pollution in Australian cities is generally low, with typical concentrations of key pollutants at much lower levels than experienced in comparable cities in many other parts of the world. Australian cities do experience occasional exceedances in ozone and PM2.5 (above air pollution guidelines), as well as extreme pollution events, often as a result of bushfires, dust storms, or heatwaves. Even in the absence of extreme events, natural emissions play a significant role in influencing the Australian urban environment, due to the remoteness from large regional anthropogenic emission sources. By studying air quality in Australia, we can gain a greater understanding of the underlying atmospheric chemistry and health risks in less polluted atmospheric environments, and the health benefits of continued reduction in air pollution. These conditions may be representative of future air quality scenarios for parts of the Northern Hemisphere, as legislation and cleaner technologies reduce anthropogenic air pollution in European, American, and Asian cities. However, in many instances, current legislation regarding emissions in Australia is significantly more lax than in other developed countries, making Australia vulnerable to worsening air pollution in association with future population growth. The need to avoid complacency is highlighted by recent epidemiological research, reporting associations between air pollution and adverse health outcomes even at air pollutant concentrations that are lower than Australia’s national air quality standards. Improving air quality is expected to improve health outcomes at any pollution level, with specific benefits projected for reductions in long-term exposure to average PM2.5 concentrations.

Abstract. In 2019–2020, Australia experienced its largest wildfire season on record. Smoke covered hundreds of square kilometers across the southeastern coast and reached the site of the COALA-2020 (Characterizing Organics and Aerosol Loading over Australia) field campaign in New South Wales. Using a subset of nighttime observations made by a proton-transfer-reaction time-of-flight mass spectrometer (PTR-ToF-MS), we calculate emission ratios (ERs) and factors (EFs) for 15 volatile organic compounds (VOCs). We restrict our analysis to VOCs with sufficiently long lifetimes to be minimally impacted by oxidation over the ∼ 8 h between when the smoke was emitted and when it arrived at the field site. We use oxidized VOC to VOC ratios to assess the total amount of radical oxidation: maleic anhydride / furan to assess OH oxidation, and (cis-2-butenediol + furanone) / furan to assess NO3 oxidation. We examine time series of O3 and NO2 given their closely linked chemistry with wildfire plumes and observe their trends during the smoke event. Then we compare ERs calculated from the freshest portion of the plume to ERs calculated using the entire nighttime period. Finding good agreement between the two, we are able to extend our analysis to VOCs measured in more chemically aged portions of the plume. Our analysis provides ERs and EFs for six compounds not previously reported for temperate forests in Australia: acrolein (a compound with significant health impacts), methyl propanoate, methyl methacrylate, maleic anhydride, benzaldehyde, and creosol. We compare our results with two studies in similar Australian biomes, and two studies focused on US temperate forests. We find over half of our EFs are within a factor of 2.5 relative to those presented in Australian biome studies, with nearly all within a factor of 5, indicating reasonable agreement. For US-focused studies, we find similar results with over half our EFs within a factor of 2.5, and nearly all within a factor of 5, again indicating reasonably good agreement. This suggests that comprehensive field measurements of biomass burning VOC emissions in other regions may be applicable to Australian temperate forests. Finally, we quantify the magnitude attributable to the primary compounds contributing to OH reactivity from this plume, finding results comparable to several US-based wildfire and laboratory studies.