Publications by authors named "Barbara Ervens"

The climate effects of atmospheric aerosol particles serving as cloud condensation nuclei (CCN) depend on chemical composition and hygroscopicity, which are highly variable on spatial and temporal scales. Here we present global CCN measurements, covering diverse environments from pristine to highly polluted conditions. We show that the effective aerosol hygroscopicity, κ, can be derived accurately from the fine aerosol mass fractions of organic particulate matter (ϵ) and inorganic ions (ϵ) through a linear combination, κ = ϵ ⋅ κ + ϵ ⋅ κ.

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The atmosphere is an integral component of the Earth's microbiome. Abundance, viability, and diversity of microorganisms circulating in the air are determined by various factors including environmental physical variables and intrinsic and biological properties of microbes, all ranging over large scales. The aeromicrobiome is thus poorly understood and difficult to predict due to the high heterogeneity of the airborne microorganisms and their properties, spatially and temporally.

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Chemical models that describe the atmospheric multiphase (gas/aqueous) system often include detailed kinetic and mechanistic schemes describing chemical reactions in both phases. The present study explores the importance of properties including the chemical composition of droplet populations, such as pH value and iron present in only a few droplets, as well as droplet size and their distribution. It is found that the assumption of evenly distributed iron in all cloud droplets leads to an underestimate by up to 1 order of magnitude of OH concentrations in the aqueous phase, whereas the predicted iron(II)/iron(total) ratio is overestimated by up to a factor of 2.

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Pyruvic acid in the atmosphere is found in both the gas and aqueous phases, and its behavior gives insight into that of other α-keto acids. Photolysis is a significant degradation pathway for this molecule in the environment, and in aqueous solution the major photoproducts are higher-molecular-weight compounds that may contribute to secondary organic aerosol mass. The kinetics of the aqueous-phase photolysis of pyruvic acid under aerobic and anaerobic conditions was investigated in order to calculate the first-order rate constant, Jaq, in solution.

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This work examines organic acid and metal concentrations in northeastern Pacific Ocean stratocumulus cloudwater samples collected by the CIRPAS Twin Otter between July and August 2011. Correlations between a suite of various monocarboxylic and dicarboxylic acid concentrations are consistent with documented aqueous-phase mechanistic relationships leading up to oxalate production. Monocarboxylic and dicarboxylic acids exhibited contrasting spatial profiles reflecting their different sources; the former were higher in concentration near the continent due to fresh organic emissions.

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The occurrence, source, and sink processes of N-nitrosodimethylamine (NDMA) have been explored by means of combined laboratory, field, and model studies. Observations have shown the occurrence of NDMA in fogs and clouds at substantial concentrations (7.5-397 ng L(-1)).

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The organic fraction of atmospheric aerosols affects the physical and chemical properties of the particles and their role in the climate system. Current models greatly underpredict secondary organic aerosol (SOA) mass. Based on a compilation of literature studies that address SOA formation, we discuss different parameters that affect the SOA formation efficiency of biogenic compounds (alpha-pinene, isoprene) and aliphatic aldehydes (glyoxal, hexanal, octanal, hexadienal).

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