Seasonal changes in carbonaceous aerosols over a tropical coastal location in response to meteorological processes

Near-surface atmospheric aerosols (PM₁₀) collected from a tropical coastal location in south-west peninsular Indian region for a duration of 6 years (2012-18) (N = 461) were analysed for carbonaceous aerosol components, the less studied aerosol species. Organic carbon (OC), its water soluble-insoluble (WSOC and WIOC) components, primary-secondary (POC and SOC) fractions and elemental carbon (EC) were examined for understanding the annual, seasonal, day-night variations in abundance pattern along with associated physical and meteorological processes. Total carbonaceous aerosols accounting for 36% of the collected aerosol mass with 31.5% organic matter (OM) and 4.5% EC respectively, exhibited consistent seasonal pattern throughout the study period with high concentration during winter followed by post-monsoon, pre-monsoon and monsoon. Delineation of marine and continental components of carbonaceous species based on their relative dominance during different air-mass periods, shows that while marine aerosols were a combination of natural sources comprising of volatile, semi-volatile species and secondary organics (from marine VOC precursors); the continental aerosols were composed of anthropogenic combustion sources (fossil fuel, biomass emissions etc). Based on the measurements of OC and EC during 2005-09 and 2012-18, their long term trends (for more than a decade) were investigated. Although OC showed an increasing tendency, EC exhibited a decrease with the total carbonaceous aerosols exhibiting a gradual decreasing trend over the years, indicating that they do not strictly reverberate the reported increasing trend observed over north-central parts of India. This can be presumed to be due to the reduced anthropogenic inputs over the location owing to the control measures and policies. The strong convective activity and large scale monsoon phenomena also helps in the effective dispersion of pollutants. Making use of comprehensive measurement of carbonaceous aerosols and the previous measurements of other aerosol components, an improved chemical composition model is presented.