Parameterization of particle formation rates in distinct atmospheric environments

Abstract. Atmospheric particle formation rate (J) is one of the key characteristics of new particle formation (NPF) processes worldwide. It is related to the development of ultrafine particle growth to cloud condensation nuclei (CCN) and, hence, Earth radiative forcing in global models, which helps us to better understand the impact of NPF on cloud properties and climate change. In this work, we parameterized four semi-empirical J models for 5 nm atmospheric particles using field measurements obtained from distinct environments that varied from clean to heavily polluted regions and from tropical to polar regions. The models rely primarily on sulfuric acid as a condensing vapor, a condensation sink to account for the vapor loss, and relative humidity for the meteorological contribution to J. However, the dependencies between J, condensation sink, and relative humidity are affected by their interlinked relations to sources and sinks of condensable vapors other than sulfuric acid and that of the potential traffic emissions to the observed size range. The parameterization results showed that our models were able to produce plausible predictions for boreal forest environments, heavily polluted environments, and biogenic environments with high relative humidity. We further tested the models in the global simulation module Tracer Model 5 (TM5, massively parallel version) to simulate the particle number size distribution across 14 global atmospheric measurement sites. The simulated results showed satisfactory predictions of particle number concentrations for all of the tested environments, with significant improvement in the nucleation mode and better prediction accuracy for the Aitken and accumulation modes compared to the binary sulfuric acid–organic vapor model in Riccobono et al. (2014). Our study has successfully provided powerful tools for predicting J5 on a global scale across various environment types using the most essential and more accessible variables involved in the NPF processes. Essentially, this work reinforces the necessity for global research into the investigation of environment-oriented meteorology-involved NPF processes.

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Publication Details

Journal
Aerosol Research
Published
2025-05-27
DOI
https://doi.org/10.5194/ar-3-271-2025
Citations
1
Primary Topic
Atmospheric chemistry and aerosols
Type
article
Field-Weighted Citation Impact
1.30

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Parameterization of particle formation rates in distinct atmospheric environments

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Parameterization of particle formation rates in distinct atmospheric environments

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article en
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Abstract

Abstract. Atmospheric particle formation rate (J) is one of the key characteristics of new particle formation (NPF) processes worldwide. It is related to the development of ultrafine particle growth to cloud condensation nuclei (CCN) and, hence, Earth radiative forcing in global models, which helps us to better understand the impact of NPF on cloud properties and climate change. In this work, we parameterized four semi-empirical J models for 5 nm atmospheric particles using field measurements obtained from distinct environments that varied from clean to heavily polluted regions and from tropical to polar regions. The models rely primarily on sulfuric acid as a condensing vapor, a condensation sink to account for the vapor loss, and relative humidity for the meteorological contribution to J. However, the dependencies between J, condensation sink, and relative humidity are affected by their interlinked relations to sources and sinks of condensable vapors other than sulfuric acid and that of the potential traffic emissions to the observed size range. The parameterization results showed that our models were able to produce plausible predictions for boreal forest environments, heavily polluted environments, and biogenic environments with high relative humidity. We further tested the models in the global simulation module Tracer Model 5 (TM5, massively parallel version) to simulate the particle number size distribution across 14 global atmospheric measurement sites. The simulated results showed satisfactory predictions of particle number concentrations for all of the tested environments, with significant improvement in the nucleation mode and better prediction accuracy for the Aitken and accumulation modes compared to the binary sulfuric acid–organic vapor model in Riccobono et al. (2014). Our study has successfully provided powerful tools for predicting J5 on a global scale across various environment types using the most essential and more accessible variables involved in the NPF processes. Essentially, this work reinforces the necessity for global research into the investigation of environment-oriented meteorology-involved NPF processes.

Aerosol ResearchVol. 3(1)
Eötvös Loránd University (HU), Finnish Meteorological Institute (FI), University of Helsinki (FI), Cyprus Institute (CY), Helsinki Institute of Physics (FI), Helsinki Institute for Information Technology (FI), Nanjing University (CN)
Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung, Academy of Finland, Horizon 2020, National Research, Development and Innovation Office, H2020 European Research Council
Openalex Percentile: Top 22%
Atmospheric chemistry and aerosols
1.30
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