Abstract

Abstract. Measurements of aerosol particle physical and chemical properties, gas phase concentrations and meteorological parameters were made along a transect in southern Indiana during the Nucleation In ForesTs (NIFTy) experiment conducted in May 2008. These measurements indicate nucleation was observed at all three measurement sites on almost half of all sampling days. The intensity of the nucleation events, as measured by the increase in ≥10 nm aerosol particle number concentrations of approximately 2×104 cm−3 over a layer of at least 300 m depth, is in good agreement with recent model results for the Midwestern USA derived using PMCAMx-UF. During the hour after termination of nucleation approximately half of the number concentration reduction is due to coagulation, while the remainder is due in equal parts to dry deposition and entrainment of relatively ultra-fine aerosol particle free troposphere air. Clear nucleation with continuous subsequent growth is only observed on days when the morning fractional cloud cover was less than 30%. It is associated with a clear transition from a strongly stratified atmosphere with low turbulence intensity and weak vertical velocities, to much a weaker vertical gradient of wind speed, increased turbulence intensity and stronger downwards vertical velocities, consistent with growth of the mixed layer and entrainment of air from the residual layer. Nucleation intensity is not very strongly determined by the prevailing condensational sink. However, there is a strong correlation between both a modified version of the Nucleation Parameter from Boy and Kulmala (2002) and ultrafine aerosol particle number concentrations, and mean morning H2SO4 concentrations and ultrafine aerosol particle number concentrations. Five A-class event days during NIFTy were characterized by values of the dimensionless nucleation parameter of Kuang et al. (2010) that are below 0.3, further indicating the applicability of their postulate that nucleation is favored by LΓ values below 0.7. Based on aerosol particle composition measurements it appears that aerosol particle formation and initial growth to approximately 30 nm diameter is dominated by ammonium and sulfate. Conservative estimates of the percent contribution of H2SO4 to aerosol particle growth (for sub-30 nm aerosol particles) on five A-class event days ranged from 23 to 85%.

Highlights

  • Introduction and objectivesAtmospheric aerosol particles affect climate both directly by scattering incoming solar radiation back to space and indirectly by acting as cloud condensation nuclei

  • – High concentrations of ultrafine aerosol particles with a diameter below 20 nm and clear growth were observed on nearly half of sampling days, and were observed at all three sampling sites

  • The observed increase of ultrafine aerosol particles at the MorganMonroe State Forest (MMSF) tower site during nucleation events is representative of increases observed through a layer of at least 300 m in depth

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Summary

Introduction and objectives

Atmospheric aerosol particles affect climate both directly by scattering incoming solar radiation back to space and indirectly by acting as cloud condensation nuclei. 8 Prior research has shown gas-to-particle conversion oc- 9 curs on regional spatial scales as indicated by ground based measurements upto several hundred kilometers apart (Dal Maso et al, 2007; Hussein et al, 2009; Jeong et al, 2010; Komppula et al, 2006; Wehner et al., 2007) These events, while nearly coincident in time, have site-specific characteristics (Hussein et al, 2009). Prior research using an aerosol mass spectrometer in Pittsburgh (east of the Ohio River Valley) showed that, during nucleation events, aerosol particles with physical diameters of 18 to 33 nm showed an initial increase in sulfate (SO24−) concentrations followed by increased ammonium (NH+4 ) concentrations (delayed by 10–40 min) and an increase in oxygenated organics (Zhang et al, 2004a), indicating a dominant role for the inorganic gases in the initial aerosol particle formation and growth at this location. To examine the chemistry of ultra-fine aerosol particle concentrations and links to gas phase chemistry during NIFTy continuous measurements of SO2, NH3, H2SO4 and timeaveraged VOC and aerosol particle composition were made at the MMSF site (Table 1)

Sampling sites
Aerosol physical characterization
Gas phase characterization
Aerosol chemical characterization
Meteorological instrumentation
Model description
Case studies of double-peak event days
Atmospheric fate of recently produced ultrafine aerosol particles
Meteorology during nucleation events
Chemical controls on nucleation
Mass closure
Findings
Concluding remarks
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