Literature DB >> 32678379

Seasonal influences on surface ozone variability in continental South Africa and implications for air quality.

Tracey Leah Laban1, Pieter Gideon van Zyl1, Johan Paul Beukes1, Ville Vakkari2, Kerneels Jaars1, Nadine Borduas-Dedekind3, Miroslav Josipovic1, Anne Mee Thompson4, Markku Kulmala5, Lauri Laakso2.   

Abstract

Although elevated surface ozone (O3) concentrations are observed in many areas within southern Africa, few studies have investigated the regional atmospheric chemistry and dominant atmospheric processes driving surface O3 formation in this region. Therefore, an assessment of comprehensive continuous surface O3 measurements performed at four sites in continental South Africa was conducted. The regional O3 problem was evident, with O3 concentrations regularly exceeding the South African air quality standard limit, while O3 levels were higher compared to other background sites in the Southern Hemisphere. The temporal O3 patterns observed at the four sites resembled typical trends for O3 in continental South Africa, with O3 concentrations peaking in late winter and early spring. Increased O3 concentrations in winter were indicative of increased emissions of O3 precursors from household combustion and other low-level sources, while a spring maximum observed at all the sites was attributed to increased regional biomass burning. Source area maps of O3 and CO indicated significantly higher O3 and CO concentrations associated with air masses passing over a region with increased seasonal open biomass burning, which indicated CO associated with open biomass burning as a major source of O3 in continental South Africa. A strong correlation between O3 on CO was observed, while O3 levels remained relatively constant or decreased with increasing NO x , which supports a VOC-limited regime. The instantaneous production rate of O3 calculated at Welgegund indicated that ~ 40 % of O3 production occurred in the VOC-limited regime. The relationship between O3 and precursor species suggests that continental South Africa can be considered VOC limited, which can be attributed to high anthropogenic emissions of NO x in the interior of South Africa. The study indicated that the most effective emission control strategy to reduce O3 levels in continental South Africa should be CO and VOC reduction, mainly associated with household combustion and regional open biomass burning.

Entities:  

Year:  2018        PMID: 32678379      PMCID: PMC7365263          DOI: 10.5194/acp-18-15491-2018

Source DB:  PubMed          Journal:  Atmos Chem Phys        ISSN: 1680-7316            Impact factor:   6.133


  5 in total

1.  Biomass burning in the tropics: impact on atmospheric chemistry and biogeochemical cycles.

Authors:  P J Crutzen; M O Andreae
Journal:  Science       Date:  1990-12-21       Impact factor: 47.728

2.  Concentrations, distributions and critical level exceedance assessment of SO2, NO2 and O3 in South Africa.

Authors:  Miroslav Josipovic; Harold J Annegarn; Melanie A Kneen; Jacobus J Pienaar; Stuart J Piketh
Journal:  Environ Monit Assess       Date:  2009-12-19       Impact factor: 2.513

3.  Reflected shock tube studies of high-temperature rate constants for OH + CH4 --> CH3 + H2O and CH3 + NO2 --> CH3O + NO.

Authors:  N K Srinivasan; M-C Su; J W Sutherland; J V Michael
Journal:  J Phys Chem A       Date:  2005-03-10       Impact factor: 2.781

4.  Tropospheric ozonesonde profiles at long-term U.S. monitoring sites: 2. Links between Trinidad Head, CA, profile clusters and inland surface ozone measurements.

Authors:  Ryan M Stauffer; Anne M Thompson; Samuel J Oltmans; Bryan J Johnson
Journal:  J Geophys Res Atmos       Date:  2016-12-06       Impact factor: 4.261

5.  Ozone profiles in the Baltimore-Washington region (2006-2011): satellite comparisons and DISCOVER-AQ observations.

Authors:  Anne M Thompson; Ryan M Stauffer; Sonya K Miller; Douglas K Martins; Everette Joseph; Andrew J Weinheimer; Glenn S Diskin
Journal:  J Atmos Chem       Date:  2014-05-14       Impact factor: 2.158

  5 in total

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