School of Geography, Earth and Atmospheric Sciences - Research Publications

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    We studied how to reduce airborne COVID spread in hospitals. Here’s what we learnt
    Buising, K ; Marshall, C ; McGain, F ; Monty, J ; Irving, L ; Kainer, M ; Schofield, R ( 2021-08-16)
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    Scenarios and Information for Policymakers
    Daniel, JS ; Reimann, S ; Ashford, P ; Fleming, EL ; Hossaini, R ; Lickley, MJ ; Schofield, R ; Walter-Terrinoni, H ; Fahey, D ; Newman, PA ; Pyle, JA ; Safari, B (World Meteorological Organization, 2022)
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    Key challenges for tropospheric chemistry in the Southern Hemisphere
    Paton-Walsh, C ; Emmerson, KM ; Garland, RM ; Keywood, M ; Hoelzemann, JJ ; Huneeus, N ; Buchholz, RR ; Humphries, RS ; Altieri, K ; Schmale, J ; Wilson, SR ; Labuschagne, C ; Kalisa, E ; Fisher, JA ; Deutscher, NM ; van Zyl, PG ; Beukes, JP ; Joubert, W ; Martin, L ; Mkololo, T ; Barbosa, C ; Andrade, MDF ; Schofield, R ; Mallet, MD ; Harvey, MJ ; Formenti, P ; Piketh, SJ ; Olivares, G (UNIV CALIFORNIA PRESS, 2022-01-07)
    This commentary paper from the recently formed International Global Atmospheric Chemistry (IGAC) Southern Hemisphere Working Group outlines key issues in atmospheric composition research that particularly impact the Southern Hemisphere. In this article, we present a broad overview of many of the challenges for understanding atmospheric chemistry in the Southern Hemisphere, before focusing in on the most significant factors that differentiate it from the Northern Hemisphere. We present sections on the importance of biogenic emissions and fires in the Southern Hemisphere, showing that these emissions often dominate over anthropogenic emissions in many regions. We then describe how these and other factors influence air quality in different parts of the Southern Hemisphere. Finally, we describe the key role of the Southern Ocean in influencing atmospheric chemistry and conclude with a description of the aims and scope of the newly formed IGAC Southern Hemisphere Working Group.
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    The contribution of coral-reef-derived dimethyl sulfide to aerosol burden over the Great Barrier Reef: a modelling study
    Fiddes, SL ; Woodhouse, MT ; Utembe, S ; Schofield, R ; Alexander, SP ; Alroe, J ; Chambers, SD ; Chen, Z ; Cravigan, L ; Dunne, E ; Humphries, RS ; Johnson, G ; Keywood, MD ; Lane, TP ; Miljevic, B ; Omori, Y ; Protat, A ; Ristovski, Z ; Selleck, P ; Swan, HB ; Tanimoto, H ; Ward, JP ; Williams, AG (COPERNICUS GESELLSCHAFT MBH, 2022-02-22)
    Abstract. Coral reefs have been found to produce the sulfur compound dimethyl sulfide (DMS), a climatically relevant aerosol precursor predominantly associated with phytoplankton. Until recently, the role of coral-reef-derived DMS within the climate system had not been quantified. A study preceding the present work found that DMS produced by corals had negligible long-term climatic forcing at the global–regional scale. However, at sub-daily timescales more typically associated with aerosol and cloud formation, the influence of coral-reef-derived DMS on local aerosol radiative effects remains unquantified. The Weather Research and Forecasting model coupled with Chemistry (WRF-Chem) has been used in this work to study the role of coral-reef-derived DMS at sub-daily timescales for the first time. WRF-Chem was run to coincide with an October 2016 field campaign over the Great Barrier Reef, Queensland, Australia, against which the model was evaluated. After updating and scaling the DMS surface water climatology, the model reproduced DMS and sulfur concentrations well. The inclusion of coral-reef-derived DMS resulted in no significant change in sulfate aerosol mass or total aerosol number. Subsequently, no direct or indirect aerosol effects were detected. The results suggest that the co-location of the Great Barrier Reef with significant anthropogenic aerosol sources along the Queensland coast prevents coral-reef-derived aerosol from having a modulating influence on local aerosol burdens in the current climate.
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    Aerosol generation related to respiratory interventions and the effectiveness of a personal ventilation hood.
    McGain, F ; Humphries, RS ; Lee, JH ; Schofield, R ; French, C ; Keywood, MD ; Irving, L ; Kevin, K ; Patel, J ; Monty, J (College of Intensive Care Medicine of Australia and New Zealand, 2020-09)
    OBJECTIVE: To quantify aerosol generation from respiratory interventions and the effectiveness of their removal by a personal ventilation hood. DESIGN AND SETTING: Determination of the aerosol particle generation (in a single, healthy volunteer in a clean room) associated with breathing, speaking, wet coughing, oxygen (O2) 15 L/min via face mask, O2 60 L/min via nasal prongs, bilevel non-invasive positive-pressure ventilation (BiPAP) and nebulisation with O2 10 L/min. INTERVENTIONS: Aerosol generation was measured with two particle sizer and counter devices, focusing on aerosols 0.5-5 μm (human-generated aerosols), with and without the hood. An increase from baseline of less than 0.3 particles per mL was considered a low level of generation. MAIN OUTCOME MEASURES: Comparisons of aerosol generation between different respiratory interventions. Effectiveness of aerosol reduction by a personal ventilation hood. RESULTS: Results for the 0.5-5 μm aerosol range. Quiet breathing and talking demonstrated very low increase in aerosols (< 0.1 particles/mL). Aerosol generation was low for wet coughing (0.1 particles/mL), O2 15 L/min via face mask (0.18 particles/mL), and high flow nasal O2 60 L/min (0.24 particles/mL). Non-invasive ventilation generated moderate aerosols (29.7 particles/mL) and nebulisation very high aerosols (1086 particles/mL); the personal ventilation hood reduced the aerosol counts by 98% to 0.5 particles/mL and 8.9 particles/mL respectively. CONCLUSIONS: In this human volunteer study, the administration of O2 15 L/min by face mask and 60 L/min nasal therapy did not increase aerosol generation beyond low levels. Non-invasive ventilation caused moderate aerosol generation and nebulisation therapy very high aerosol generation. The personal ventilation hood reduced the aerosol counts by at least 98%.
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    Effectiveness of portable air filtration on reducing indoor aerosol transmission: preclinical observational trials
    Lee, JH ; Rounds, M ; McGain, F ; Schofield, R ; Skidmore, G ; Wadlow, I ; Kevin, K ; Stevens, A ; Marshall, C ; Irving, L ; Kainer, M ; Buising, K ; Monty, J (W B SAUNDERS CO LTD, 2022-01)
    BACKGROUND: While the range of possible transmission pathways of severe acute respiratory syndrome coronavirus-2 in various settings has been investigated thoroughly, most authorities have recently acknowledged the role of aerosol spread in its transmission, especially in indoor environments where ventilation is poor. Engineering controls are needed to mitigate aerosol transmission in high-risk settings including hospital wards, classrooms and offices. AIM: To assess the effectiveness of aerosol filtration by portable air cleaning devices with high-efficiency particulate air filters used in addition to a standard building heating ventilation and air conditioning (HVAC) system. METHODS: Test rooms, including a single-bed hospital room, were filled with test aerosol to simulate aerosol movement. Aerosol counts were measured over time with various portable air cleaning devices and room ventilation systems to quantify the overall aerosol clearance rate. FINDINGS: Portable air cleaning devices were very effective for removal of aerosols. The aerosols were cleared five times faster in a small control room with portable air cleaning devices than in the room with HVAC alone. The single-bed hospital room had an excellent ventilation rate (∼14 air changes per hour) and cleared the aerosols in 20 min. However, with the addition of two air cleaning devices, the clearance time was three times faster. CONCLUSIONS: Inexpensive portable air cleaning devices should be considered for small and enclosed spaces in healthcare settings, such as inpatient rooms and personal protective equipment donning/doffing stations. Portable air cleaning devices are particularly important where there is limited ability to reduce aerosol transmission with building HVAC ventilation.
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    High-resolution modeling of gaseous air pollutants over Tehran and validation with surface and satellite data
    Shahrokhishahraki, N ; Rayner, PJ ; Silver, JD ; Thomas, S ; Schofield, R (PERGAMON-ELSEVIER SCIENCE LTD, 2022-02-01)
    This study addresses the question of how skillful regional air quality modeling can be when using downscaled globally-available emission inventories. This paper applies global datasets to prepare fine-resolution priori emission inventories for an urban area. Emissions Database for Global Atmospheric Research (EDGAR), Gridded Population of the World, and output from the Fossil Fuel Data Assimilation System are used to downscale the spatiotemporal resolution of global emission inventories to the finer scale. The resultant high-resolution inventory is taken as input for an off-line run of the Community Multi-Scale Air Quality (CMAQ) modeling system to simulate the concentrations of air pollutants in Tehran during August 2018, November 2018, February 2019, and May 2019. These runs are forced with meteorology from the Weather Research and Forecasting (WRF) model. Retrievals of atmospheric composition from the TROPOspheric Monitoring Instrument (TROPOMI) and surface measurements (split into ‘road’ or ‘city’ type stations) are used to compare with the modeled concentrations of NO2, CO, and O3 to assess the capability of the applied modeling framework and emission inventories in concentration estimations. Comparison of modeled NO2 concentration with NO2 tropospheric column shows that the model captures the spatial and temporal distribution with Pearson correlation above 0.7 and 0.6, respectively and absolute bias under 0.08 ppb. The offline WRF-CMAQ simulations overestimate surface measurements of NO2 and CO and underestimate O3. The model captures the diurnal variations for NO2, CO, and O3 with a correlation between 0.7 and 0.91, 0.6–0.8, and 0.5–0.98 and absolute bias less than 69 ppb, 1.15 ppm, and 12.5 ppb, respectively. The overall performance of the observing and modeling system is sufficient for a credible inversion of surface emissions, which is the intended purpose of this modeling set-up.
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    Future changes in stratospheric quasi-stationary wave-1 in the extratropical southern hemisphere spring and summer as simulated by ACCESS-CCM
    Stone, KA ; Klekociuk, AR ; Schofield, R (CSIRO PUBLISHING, 2021)
    Seasonally dependent quasi-stationary planetary wave activity in the southern hemisphere influences the distribution of ozone within and near the equatorward edge of the stratospheric polar vortex. Accurate representation of this zonal asymmetry in ozone is important in the characterisation of stratospheric circulation and climate and their associated effects at the surface. In this study, we used the Australian Community and Climate Earth System Simulator-Chemistry Climate Model to investigate the influence of greenhouse gases (GHGs) and ozone depleting substances (ODSs) on the zonal asymmetry of total column ozone (TCO) and 10 hPa zonal wind between 50 and 70°S. Sensitivity simulations were used from 1960 to 2100 with fixed ODSs and GHGs at 1960 levels and a regression model that uses equivalent effective stratospheric chlorine and carbon dioxide equivalent radiative forcing as the regressors. The model simulates the spring and summer zonal wave-1 reasonably well, albeit with a slight bias in the phase and amplitude compared to observations. An eastward shift in the TCO and 10 hPa zonal wave-1 is associated with both decreasing ozone and increasing GHGs. Amplitude increases are associated with ozone decline and amplitude decreases with GHG increases. The influence of ODSs typically outweigh those by GHGs, partly due to the GHG influence on TCO phase at 50°S likely being hampered by the Andes. Therefore, over the 21st century, influence from ozone recovery causes a westward shift and a decrease in amplitude. An exception is at 70°S during spring, where the GHG influence is larger than that of ozone recovery, causing a continued eastward trend throughout the 21st century. Also, GHGs have the largest influence on the 10 hPa zonal wave-1 phase, but still only induce a small change in the wave-1 amplitude. Different local longitudes also experience different rates of ozone recovery due to the changes in phase of the zonal wave-1. The results from this study have important implications for understanding future ozone layer distribution in the Southern Hemisphere under changing GHG and ODS concentrations. Important future work would involve conducting a similar study using a large ensemble of models to gain more statistically significant results.