Abstract

Abstract. Some types of biological particles are known to nucleate ice at warmer temperatures than mineral dust, with the potential to influence cloud microphysical properties and climate. However, the prevalence of these particle types above the atmospheric boundary layer is not well known. Many types of biological particles fluoresce when exposed to ultraviolet light, and the Wideband Integrated Bioaerosol Sensor takes advantage of this characteristic to perform real-time measurements of fluorescent biological aerosol particles (FBAPs). This instrument was flown on the National Center for Atmospheric Research Gulfstream V aircraft to measure concentrations of fluorescent biological particles from different potential sources and at various altitudes over the US western plains in early autumn. Clear-air number concentrations of FBAPs between 0.8 and 12 µm diameter usually decreased with height and generally were about 10–100 L−1 in the continental boundary layer but always much lower at temperatures colder than 255 K in the free troposphere. At intermediate temperatures where biological ice-nucleating particles may influence mixed-phase cloud formation (255 K ≤ T ≤ 270 K), concentrations of fluorescent particles were the most variable and were occasionally near boundary-layer concentrations. Predicted vertical distributions of ice-nucleating particle concentrations based on FBAP measurements in this temperature regime sometimes reached typical concentrations of primary ice in clouds but were often much lower. If convection was assumed to lift boundary-layer FBAPs without losses to the free troposphere, better agreement between predicted ice-nucleating particle concentrations and typical ice crystal concentrations was achieved. Ice-nucleating particle concentrations were also measured during one flight and showed a decrease with height, and concentrations were consistent with a relationship to FBAPs established previously at the forested surface site below. The vertical distributions of FBAPs measured on five flights were also compared with those for bacteria, fungal spores, and pollen predicted from the EMAC global chemistry–climate model for the same geographic region.

Highlights

  • Details of the formation of ice in clouds are poorly understood, especially considering the importance of this phase transition to cloud evolution, climate, and the cycling of water and trace constituents in Earth’s atmosphere

  • The concentrations of ice-nucleating particles measured by a droplet freezing apparatus and by a continuous-flow diffusion chamber were found to be correlated with concentrations of biological particles at this forested site (Huffman et al, 2013; Tobo et al, 2013)

  • We present fluorescent biological particle concentrations and ice-nucleating particle (INP) concentrations from filter measurements taken on the aircraft over the forested site and compare them with similar measurements taken simultaneously on the ground and at the canopy top

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Summary

Introduction

Details of the formation of ice in clouds are poorly understood, especially considering the importance of this phase transition to cloud evolution, climate, and the cycling of water and trace constituents in Earth’s atmosphere. Water droplets can remain supercooled at temperatures below. 273 K, and the presence of an ice-nucleating particle (INP) reduces the energy barrier required for the phase transformation from liquid to ice. Biological particles have received much interest in the community recently because certain ones tend to nucleate ice efficiently at warmer temperatures than mineral dust particles (Murray et al, 2012). While laboratory studies show mineral dust and some types of biological particles can act as INPs, there is conflicting evidence regarding the importance of biological particles as INPs in the atmosphere (Després et al, 2012). Modeling studies suggest that biological INPs are not very important globally, mainly because their concentrations at cold cloud levels are thought to be relatively low compared to other INPs like mineral dust (Hoose et al, 2010)

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