[1] A major source of the primary marine aerosol is the bursting of air bubbles produced by breaking waves. Several source parameterizations are available from the literature, usually limited to particles with a dry diameter D p > 1 mm. The objective of this work is to extend the current knowledge to submicrometer particles. Bubbles were generated in synthetic seawater using a sintered glass filter, with a size spectra that are only partly the same spectra as measured in the field. Bubble spectra, and size distributions of the resulting aerosol (0.020-20.0 mm D p ) of the resulting aerosol, were measured for different salinity, water temperature (T w ), and bubble flux. The spectra show a minimum at $1 mm D p , which separates two modes, one at $0.1 mm, with the largest number of particles, and one at 2.5 mm D p . The modes show different behavior with the variation of salinity and water temperature. When the water temperature increases, the number concentration N p decreases for D p < 0.07 mm, whereas for D p > 0.35 mm, N p increases. The salinity effect suggests different droplet formation processes for droplets smaller and larger than 0.2 mm D p . The number of particles produced per size increment, time unit, and whitecap surface (È) is described as a linear function of T w and a polynomial function of D p . Combining È with the whitecap coverage fraction W (in percent), an expression results for the primary marine aerosol source flux dF 0 /dlogD p = W È (m À2 s À1 ). The results are compared with other commonly used formulations as well as with recent field observations. Implications for aerosol-induced effects on climate are discussed.
Aerosols play a key role in the radiation balance of the atmosphere. Here, we present evidence that the European boreal region is a substantial source of both aerosol mass and aerosol number. The investigation supplies a straightforward relation between emissions of monoterpenes and gas-to-particle formation over regions substantially lacking in anthropogenic aerosol sources. Our results show that the forest provides an aerosol population of 1000 to 2000 particles of climatically active sizes per cubic centimeter during the late spring to early fall period. This has important implications for radiation budget estimates and relevancy for the evaluation of feedback loops believed to determine our future climate.
A B S T R A C TThe hygroscopic properties play a vital role for the direct and indirect effects of aerosols on climate, as well as the health effects of particulate matter (PM) by modifying the deposition pattern of inhaled particles in the humid human respiratory tract. Hygroscopic Tandem Differential Mobility Analyzer (H-TDMA) instruments have been used in field campaigns in various environments globally over the last 25 yr to determine the water uptake on submicrometre particles at subsaturated conditions. These investigations have yielded valuable and comprehensive information regarding the particle hygroscopic properties of the atmospheric aerosol, including state of mixing. These properties determine the equilibrium particle size at ambient relative humidities and have successfully been used to calculate the activation of particles at water vapour supersaturation. This paper summarizes the existing published H-TDMA results on the sizeresolved submicrometre aerosol particle hygroscopic properties obtained from ground-based measurements at multiple marine, rural, urban and free tropospheric measurement sites. The data is classified into groups of hygroscopic growth indicating the external mixture, and providing clues to the sources and processes controlling the aerosol. An evaluation is given on how different chemical and physical properties affect the hygroscopic growth.
Abstract. The European Aerosol Cloud Climate and Air Quality Interactions project EUCAARI is an EU ResearchFramework 6 integrated project focusing on understanding the interactions of climate and air pollution. EUCAARI works in an integrative and multidisciplinary way from nanoto global scale. EUCAARI brings together several leading European research groups, state-of-the-art infrastructure and some key scientists from third countries to investigate the role of aerosol on climate and air quality. Altogether 48 partners from 25 countries are participating in EUCAARI. During the first 16 months EUCAARI has built operational systems, e.g. established pan-European measurement network for Lagrangian studies and four stations in developing countries. Also an improved understanding of nanoscale processes (like nucleation) has been implemented in global models. Here we present the research methods, organisation, operations and first results of EUCAARI.Correspondence to: M. Kulmala
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