Abstract

Abstract. Secondary new particle formation affects atmospheric aerosol and cloud droplet numbers and thereby, the aerosol effects on climate. In this paper, the frequency of nucleation events and the associated particle formation and growth rates, along with their seasonal variation, was analysed based on over ten years of aerosol measurements conducted at the Pallas GAW station in northern Finland. The long-term measurements also allowed a detailed examination of factors possibly favouring or suppressing particle formation. Effects of meteorological parameters and air mass properties as well as vapour sources and sinks for particle formation frequency and event parameters were inspected. In addition, the potential of secondary particle formation to increase the concentration of cloud condensation nuclei (CCN) sized particles was examined. Findings from these long-term measurements confirmed previous observations: event frequency peaked in spring and the highest growth rates were observed in summer, affiliated with increased biogenic activity. Events were almost exclusively observed in marine air masses on sunny cloud-free days. A low vapour sink by the background particle population as well as an elevated sulphuric acid concentration were found to favour particle formation. These were also conditions taking place most likely in marine air masses. Inter-annual trend showed a minimum in event frequency in 2003, when also the smallest annual median of growth rate was observed. This gives further evidence of the importance and sensitivity of particle formation for the condensing vapour concentrations at Pallas site. The particle formation was observed to increase CCN80 (>80 nm particle number) concentrations especially in summer and autumn seasons when the growth rates were the highest. When the growing mode exceeded the selected 80 nm limit, on average in those cases, 211 ± 114% increase of CCN80 concentrations was observed.

Highlights

  • Atmospheric new particle formation (NPF) has been observed to take place in a vast variety of environments, including clean and polluted continental boundary layers, coastal and some other marine areas, anthropogenic plumes, cloud outflows and free troposphere (Kulmala et al, 2004; Kulmala and Kerminen, 2008; O’Dowd et al, 2010)

  • I NPF events used in FR7 and growth rates (GR) calculations

  • Tchleealatsitoconlumn shows the total number (n) of class I NPF events used in FR7 and GR calculations

Read more

Summary

Introduction

Atmospheric new particle formation (NPF) has been observed to take place in a vast variety of environments, including clean and polluted continental boundary layers, coastal and some other marine areas, anthropogenic plumes, cloud outflows and free troposphere (Kulmala et al, 2004; Kulmala and Kerminen, 2008; O’Dowd et al, 2010). The rate of NPF appears to scale between the first and second power of the gaseous sulphuric acid concentration, being indicative of either activation (Kulmala et al, 2006) or kinetic-type (McMurry and Friedlander, 1979) formation process. The role of ions in atmospheric NPF has remained the subject of large debate (Gagneet al., 2010; Hirsikko et al, 2011; Kazil et al, 2008; Yu, 2010a)

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call