Abstract

Abstract. Measurements of size-resolved cloud condensation nuclei (CCN) concentrations, subsaturated hygroscopic growth, size distribution, and chemical composition were collected from March through May, 2007, in the remote Boreal forests of Hyytiälä, Finland, as part of the European Integrated project on Aerosol Cloud Climate and Air Quality Interactions (EUCAARI) campaign. Hygroscopicity parameter, κ, distributions were derived independently from Continuous Flow-Streamwise Thermal Gradient CCN Chamber (CFSTGC) and Hygroscopicity Tandem Differential Mobility Analyzer (HTDMA) measurements. CFSTGC-derived κ values for 40, 60, and 80 nm particles range mostly between 0.10 and 0.40 with an average characteristic of highly oxidized organics of 0.20 ± 0.10, indicating that organics play a dominant role for this environment. HTDMA-derived κ were generally 30% lower. Diurnal trends of κ show a minimum at sunrise and a maximum in the late afternoon; this trend covaries with inorganic mass fraction and the m/z 44 organic mass fraction given by a quadrupole aerosol mass spectrometer, further illustrating the importance of organics in aerosol hygroscopicity. The chemical dispersion inferred from the observed κ distributions indicates that while 60 and 80 nm dispersion increases around midday, 40 nm dispersion remains constant. Additionally, 80 nm particles show a markedly higher level of chemical dispersion than both 40 and 60 nm particles. An analysis of droplet activation kinetics for the sizes considered indicates that most of the CCN activate as rapidly as (NH4)2SO4 calibration aerosol.

Highlights

  • Atmospheric aerosols are known to have a direct effect on climate through scattering and absorbing incoming solar radiation (IPCC, 2007)

  • The cloud condensation nuclei (CCN) counter detects only those particles that are activated which means that non-hygroscopic particles do not impact the slope of the sigmoid used to calculate s∗

  • Hygroscopicity Tandem Differential Mobility Analyzer (HTDMA)-derived κ values from this study are in agreement with the HTDMA-derived average κ = 0.18 for 35, 50, 75, and 110 nm particles reported for this region by Sihto et al (2010) for July 2008 to June 2009

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Summary

Introduction

Atmospheric aerosols are known to have a direct effect on climate through scattering and absorbing incoming solar radiation (IPCC, 2007) They indirectly affect climate by acting as cloud condensation nuclei (CCN), and modifying cloud forcing and the hydrological cycle (Twomey, 1974, 1977). While it is generally thought that aerosols produce an overall cooling effect, the indirect effect remains a large source of uncertainty in predictions of anthropogenic climate change (e.g., IPCC, 2007). For this reason, the study of aerosol and their CCN properties is necessary for an improved understanding of aerosol-cloud-climate interactions.

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