Aircraft observations of aerosol composition and ageing in New England and Mid-Atlantic States during the summer 2002 New England Air Quality Study field campaign

Aerosol chemical composition, size distribution, and optical properties were measured during 17 aircraft flights in New England and Middle Atlantic States as part of the summer 2002 New England Air Quality Study field campaign. An Aerodyne aerosol mass spectrometer ( AMS) was operated with a measurement cycle of 30 s, about an order of magnitude faster than used for ground-based measurements. Noise levels within a single measurement period were sub mu g m(-3). Volume data derived from the AMS were compared with volume measurements from a Passive Cavity Aerosol Spectrometer ( PCASP) optical particle detector and a Twin Scanning Electrical Mobility Spectrometer ( TSEMS); calculated light scattering was compared with measured values from an integrating nephelometer. The median ratio for AMS/TSEMS volume was 1.25 ( 1.33 with an estimated refractory component); the median ratio for AMS/nephelometer scattering was 1.18. A dependence of the AMS collection efficiency on aerosol acidity was quantified by a comparison between AMS and PCASP volumes in two high sulfate plumes. For the entire field campaign, the average aerosol concentration was 11 mu g m(-3). Compared with monitoring data from the IMPROVE network, the organic component made up a large fraction of total mass, varying from 70% in clean air to 40% in high concentration sulfate plumes. In combination with other optical and chemical measurements, the AMS gave information on secondary organic aerosol ( SOA) production and the time evolution of aerosol light absorption. CO is taken as a conservative tracer of urban emissions and the ratios of organic aerosol and aerosol light absorption to CO examined as a function of photochemical age. Comparisons were made to ratios determined from surface measurements under conditions of minimal atmospheric processing. In air masses in which the NOx to NOy ratio has decreased to 10%, the ratio of organic aerosol to CO has quadrupled indicating that 75% of the organic aerosol is secondary. Also, the ratio of light absorption to CO has more than doubled, which is interpreted as an equivalent increase in the light absorption efficiency of black carbon due to aerosol ageing.