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Abstract A key challenge in aerosol pollution studies and climate change assessment is to understand how atmospheric aerosol particles are initially formed^1,2. Although new particle formation (NPF) mechanisms have been described at specific sites^3–6, in most regions, such mechanisms remain uncertain to a large extent because of the limited ability of atmospheric models to simulate critical NPF processes^1,7. Here we synthesize molecular-level experiments to develop comprehensive representations of 11 NPF mechanisms and the complex chemical transformation of precursor gases in a fully coupled global climate model. Combined simulations and observations show that the dominant NPF mechanisms are distinct worldwide and vary with region and altitude. Previously neglected or underrepresented mechanisms involving organics, amines, iodine oxoacids and HNO₃probably dominate NPF in most regions with high concentrations of aerosols or large aerosol radiative forcing; such regions include oceanic and human-polluted continental boundary layers, as well as the upper troposphere over rainforests and Asian monsoon regions. These underrepresented mechanisms also play notable roles in other areas, such as the upper troposphere of the Pacific and Atlantic oceans. Accordingly, NPF accounts for different fractions (10–80%) of the nuclei on which cloud forms at 0.5% supersaturation over various regions in the lower troposphere. The comprehensive simulation of global NPF mechanisms can help improve estimation and source attribution of the climate effects of aerosols. 

Abstract Understanding the formation processes of particles and cloud condensation nuclei (CCN) in pristine environments is a major challenge in assessing the anthropogenic impacts on climate change. Using a state‐of‐the‐art model that systematically simulates the new‐particle formation (NPF) from condensable vapors and multi‐scale transport of chemical species, we find that NPF contributes ∼90% of the particle number and ∼80% of the CCN at 0.5% supersaturation (CCN0.5%) in the pristine Amazon boundary layer during the wet season. The corresponding contributions are only ∼30% and ∼20% during the dry season because of prevalent biomass burning. In both seasons, ∼50% of the NPF‐induced particles and ∼85% of the NPF‐induced CCN0.5% in the boundary layer originate from the long‐range transport of new particles formed hundreds to thousands of kilometers away. Moreover, about 50%–65% of the NPF‐induced particles and 35%–50% of the NPF‐induced CCN0.5% originate from the downward transport of new particles formed aloft.