Suchergebnisse

Particle mass concentrations (PM10, PM2.5 and PM1) and particle number concentration ((PNC); 0.27 μm ≤ Dp ≤ 34.00 μm) were measured in the tropical coastal environment of Bachok, Kelantan on the Malaysian Peninsula bordering the southern edge of the South China Sea. Statistical methods were applied on a three-month hourly data set (9th January to 24th March 2014) to study the influence of north-easterly winds on the patterns of particle mass and PNC size distributions. The 24-h concentrations of particle mass obtained in this study were below the standard values detailed by the Recommended Malaysian Air Quality Guideline (RMAQG), United States Environmental Protection Agency (US EPA) and European Union (EU) except for PM2.5, which recorded a 24-h average of 30 ± 18 μg m-3 and exceeded the World Health Organisation (WHO) threshold value (25 μg m-3). Principal component analysis (PCA) revealed that PNC with smaller diameter sizes (0.27-4.50 μm) showed a stronger influence, accounting for 57.6% of the variability in PNC data set. Concentrations of both particle mass and PNC increased steadily in the morning with a distinct peak observed at around 8.00 h, related to a combination of dispersion of accumulated particles overnight and local traffic. In addition to local anthropogenic, agricultural burning and forest fire activities, long-range transport also affects the study area. Hotspot and backward wind trajectory observations illustrated that the biomass burning episode (around February-March) significantly influenced PNC. Meteorological parameters influenced smaller size particles (i.e. PM1 and Dp (0.27-0.43 μm)) the most.

Secondary organic aerosol (SOA) accounts for a dominant fraction of the submicron atmospheric particle mass, but knowledge of the formation, composition and climate effects of SOA is incomplete and limits our understanding of overall aerosol effects in the atmosphere. Organic oligomers were discovered as dominant components in SOA over a decade ago in laboratory experiments and have since been proposed to play a dominant role in many aerosol processes. However, it remains unclear whether oligomers are relevant under ambient atmospheric conditions because they are often not clearly observed in field samples. Here we resolve this long-standing discrepancy by showing that elevated SOA mass is one of the key drivers of oligomer formation in the ambient atmosphere and laboratory experiments. We show for the first time that a specific organic compound class in aerosols, oligomers, is strongly correlated with cloud condensation nuclei (CCN) activities of SOA particles. These findings might have important implications for future climate scenarios where increased temperatures cause higher biogenic volatile organic compound (VOC) emissions, which in turn lead to higher SOA mass formation and significant changes in SOA composition. Such processes would need to be considered in climate models for a realistic representation of future aerosol-climate-biosphere feedbacks. ; Research at the University of Cambridge was supported by a Marie Curie Intra-European fellowship (project no. 254319) and the ERC grant no. 279405. We thank the SAPHIR and TNA2012 team in Jülich for supporting our measurements and the support by EUROCHAMP2 contract no. 228335. The field-work was funded by ERC grant 227463 and the Academy of Finland Centre of Excellence (grants 1118615 and 272041) and by the Office of Science (BER), US Department of Energy via Biogenic Aerosols - Effects on Clouds and Climate (BAECC). European Union's Horizon 2020 research and innovation programme under grant agreement no. 654109 and previously from the European Union Seventh Framework Programme (FP7/2007-2013) under grant agreement no. 262254. We thank the Met Office for use of the NAME model. S.C. thanks the UK Natural Environment Research Council for her studentship.