Articles | Volume 22, issue 20
https://doi.org/10.5194/acp-22-13659-2022
© Author(s) 2022. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/acp-22-13659-2022
© Author(s) 2022. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Research article
| 
21 Oct 2022
Research article |
| 21 Oct 2022
| 21 Oct 2022
Global distribution of Asian, Middle Eastern, and North African dust simulated by CESM1/CARMA
Siying Lian
Institute for Environmental and Climate Research, Jinan University, Guangzhou, China
Luxi Zhou
Guangzhou Institute of Tropical and Marine Meteorology, Meteorological Administration, Guangzhou, China
Daniel M. Murphy
Chemical Science Laboratory, National Oceanic and Atmospheric
Administration, Boulder, Colorado, USA
Karl D. Froyd
Chemical Science Laboratory, National Oceanic and Atmospheric
Administration, Boulder, Colorado, USA
Owen B. Toon
Department of Atmospheric and Oceanic Sciences and Laboratory for
Atmospheric and Space Physics, University of Colorado Boulder, Boulder, Colorado, USA
Institute for Environmental and Climate Research, Jinan University, Guangzhou, China
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Matthias Kohl, Christoph Brühl, Holger Tost, Christos Xenofontos, Theodoros Christoudias, Sergey Gromov, Oliver Appel, Stephan Borrmann, Adam Bourassa, Pedro Campunzano-Jost, Yafang Cheng, Oliver Eppers, Karl D. Froyd, Bruna A. Holanda, Jose L. Jimenez, Patrick Jöckel, Philipp Joppe, Katharina Kaiser, Joseph M. Katich, Klaus Klingmüller, Franziska Köllner, Agnieszka Kupc, Anna Martin, Christopher Pöhlker, Mira L. Pöhlker, Ulrich Pöschl, Landon Rieger, Samuel Ruhl, Gregory P. Schill, Johannes Schneider, Christiane Schulz, Joshua P. Schwarz, Alexandra P. Tsimpidi, Ryan Vella, Christina J. Williamson, Yifan Yang, Daniel Zawada, Jos Lelieveld, and Andrea Pozzer
EGUsphere, https://doi.org/10.5194/egusphere-2026-3649, https://doi.org/10.5194/egusphere-2026-3649, 2026
This preprint is open for discussion and under review for Atmospheric Chemistry and Physics (ACP).
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Aerosols are crucial for Earth's climate, yet their vertical distribution remains poorly understood. We present first consistent global simulations of aerosol distributions and composition from the Earth's surface to the stratosphere, validated by extensive observations. Key findings include a global minimum in aerosol mass in the free troposphere, a significant contribution of organic aerosol in the lower stratosphere, and limited transport of primary particles to the stratosphere.
Ilaria Quaglia, Daniele Visioni, Ewa M. Bednarz, Yunqian Zhu, Georgiy Stenchikov, Valentina Aquila, Cheng-Cheng Liu, Graham W. Mann, Yifeng Peng, Takashi Sekiya, Simone Tilmes, Xinyue Wang, Shingo Watanabe, Pengfei Yu, Jun Zhang, Wandi Yu, and Zhihong Zhuo
Atmos. Chem. Phys., 26, 7677–7704, https://doi.org/10.5194/acp-26-7677-2026, https://doi.org/10.5194/acp-26-7677-2026, 2026
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On January 15, 2022, the Hunga volcano eruption released unprecedented amounts of water vapor into the atmosphere alongside a modest amount of SO2. In this work we analyse results from multiple Earth system models. The models agree that the eruption led to small negative radiative forcing from sulfate aerosols and that the contribution from water vapor was minimal. Therefore, the Hunga eruption cannot explain the exceptional surface warming observed in 2023.
Larissa Lacher, A. Gannet Hallar, Ian B. McCubbin, Joey Bail, Karl D. Froyd, Justin Jacquot, Xiaoli Shen, Christopher Rapp, Ottmar Möhler, and Daniel Cziczo
Atmos. Chem. Phys., 26, 6703–6726, https://doi.org/10.5194/acp-26-6703-2026, https://doi.org/10.5194/acp-26-6703-2026, 2026
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We observe a trend of increasing ice-nucleating particle (INP) concentration in spring in the Rocky Mountains, related to regional dust emissions that may intensify with climate change. Additionally, super-micrometer particles were found as the most important contributors to the INP population. This finding was partly enabled by a novel setup of the Portable Ice Nucleation Experiment (PINE), coupled with a pumped-counterflow virtual impactor allowing for direct analysis of INP properties.
Simone Tilmes, Daniele Visioni, Ilaria Quaglia, Yunqian Zhu, Charles G. Bardeen, Francis Vitt, and Pengfei Yu
Atmos. Chem. Phys., 26, 2649–2666, https://doi.org/10.5194/acp-26-2649-2026, https://doi.org/10.5194/acp-26-2649-2026, 2026
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This study compares two sets of stratospheric aerosol injection (SAI) experiments using the same modeling framework, differing only in their aerosol microphysical schemes. Results show that these two schemes can yield substantially different aerosol burdens, radiative changes, and impacts when simulating the same injection scenarios. These findings suggest that more sophisticated aerosol models may be necessary to accurately assess the efficacy, side effects, and climate impacts of SAI.
Wenhui Zhao, Weiwei Hu, Zhaoce Liu, Tianle Pan, Tingting Feng, Jun Wang, Yiyu Cai, Lin Liang, Shan Huang, Bin Yuan, Nan Ma, Min Shao, Guohua Zhang, Xinhui Bi, Xinming Wang, and Pengfei Yu
Atmos. Chem. Phys., 26, 135–154, https://doi.org/10.5194/acp-26-135-2026, https://doi.org/10.5194/acp-26-135-2026, 2026
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Our study examined brown carbon – organic aerosols that absorb light – at the remote Tibet and urban Guangzhou. Field data showed Tibet’s brown carbon absorbs about 10 times less than Guangzhou’s, due to cleaner air. Yet, over 75 % of its light absorption still comes from primary emission, which causes over 98 % of its climate-warming effect in both places. This study advances understanding of brown carbon dynamics and its sources in diverse environments for global climate effects.
Pengfei Yu, Yifeng Peng, Karen H. Rosenlof, Ru-Shan Gao, Robert W. Portmann, Martin Ross, Eric Ray, Jianchun Bian, Simone Tilmes, and Owen B. Toon
Atmos. Chem. Phys., 25, 18449–18460, https://doi.org/10.5194/acp-25-18449-2025, https://doi.org/10.5194/acp-25-18449-2025, 2025
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Injecting sulfur dioxide at 50 km – near the stratopause – offers a far safer and more effective climate intervention than conventional 25 km injection. Rapid downward–poleward transport distributes aerosols across 20–30 km, halving tropical stratospheric warming, reducing ozone recovery delays from decades to about 5 years, and enhancing global and polar cooling by over 20 %, while better preserving Arctic sea ice.
Weichao Huang, Sihang Wang, Peng Cheng, Bingna Chen, Bin Yuan, Pengfei Yu, Haichao Wang, Nan Ma, Mei Li, and Keding Lu
Atmos. Chem. Phys., 25, 15403–15414, https://doi.org/10.5194/acp-25-15403-2025, https://doi.org/10.5194/acp-25-15403-2025, 2025
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We studied vehicle emissions from ten 3000-meter tunnels on the Tibetan Plateau. Emissions of volatile organic compounds (VOCs) increase with elevation due to the evaporation of fuel oil from low pressure, unlike at lower elevations where tailpipe is predominant. This suggests that specific emission control measures are needed. This research aims to understand emissions at high altitudes and to guide cleaner transport.
Kasper Juurikkala, Christina J. Williamson, Karl D. Froyd, Jonathan Dean-Day, and Ari Laaksonen
Atmos. Chem. Phys., 25, 13995–14013, https://doi.org/10.5194/acp-25-13995-2025, https://doi.org/10.5194/acp-25-13995-2025, 2025
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This study uses Large Eddy Simulations (LES) to investigate synoptic cirrus clouds from NASA’s Mid-latitude Airborne Cirrus Properties Experiment (MACPEX) campaign. Results show that prior heterogeneous ice nucleation depletes ice nuclei, creating conditions for subsequent homogeneous freezing. The findings highlight limitations of ice residual analysis in capturing cirrus evolution and provide insights into aerosol-cloud interactions critical to atmospheric and climate processes.
Xueqin Zheng, Junwen Liu, Nima Chuduo, Bian Ba, Pengfei Yu, Phu Drolgar, Fang Cao, and Yanlin Zhang
Atmos. Chem. Phys., 25, 12451–12465, https://doi.org/10.5194/acp-25-12451-2025, https://doi.org/10.5194/acp-25-12451-2025, 2025
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In this study, we present the first report on the annual variation of stable oxygen isotope anomalies in nitrate (NO3−) collected from the urban area of Lhasa, on the Tibetan Plateau, China. Using a Bayesian isotope mixture model, we found that the relative contribution of the NO3 + volatile organic compound (VOC) pathway to NO3− formation in spring in Lhasa was several times higher than that in urban cities, highlighting the significant influence of VOCs transported from outside the Tibetan Plateau.
Yunqian Zhu, Hideharu Akiyoshi, Valentina Aquila, Elizabeth Asher, Ewa M. Bednarz, Slimane Bekki, Christoph Brühl, Amy H. Butler, Parker Case, Simon Chabrillat, Gabriel Chiodo, Margot Clyne, Peter R. Colarco, Sandip Dhomse, Lola Falletti, Eric Fleming, Ben Johnson, Andrin Jörimann, Mahesh Kovilakam, Gerbrand Koren, Ales Kuchar, Nicolas Lebas, Qing Liang, Cheng-Cheng Liu, Graham Mann, Michael Manyin, Marion Marchand, Olaf Morgenstern, Paul Newman, Luke D. Oman, Freja F. Østerstrøm, Yifeng Peng, David Plummer, Ilaria Quaglia, William Randel, Samuel Rémy, Takashi Sekiya, Stephen Steenrod, Timofei Sukhodolov, Simone Tilmes, Kostas Tsigaridis, Rei Ueyama, Daniele Visioni, Xinyue Wang, Shingo Watanabe, Yousuke Yamashita, Pengfei Yu, Wandi Yu, Jun Zhang, and Zhihong Zhuo
Geosci. Model Dev., 18, 5487–5512, https://doi.org/10.5194/gmd-18-5487-2025, https://doi.org/10.5194/gmd-18-5487-2025, 2025
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To understand the climate impact of the 2022 Hunga volcanic eruption, we developed a climate model–observation comparison project. The paper describes the protocols and models that participate in the experiments. We designed several experiments to achieve our goals of this activity: (1) to evaluate the climate model performance and (2) to understand the Earth system responses to this eruption.
Kane Stone, Susan Solomon, Pengfei Yu, Daniel M. Murphy, Douglas Kinnison, and Jian Guan
Atmos. Chem. Phys., 25, 7683–7697, https://doi.org/10.5194/acp-25-7683-2025, https://doi.org/10.5194/acp-25-7683-2025, 2025
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The Australian 2019–2020 wildfires injected a substantial amount of smoke into the upper atmosphere, causing unusual chemical reactions that altered the chemical makeup of the upper atmosphere. This led to ozone depletion in the Southern Hemisphere midlatitudes that likely did not fully recover until 2 years after the initial event due to the persistent chemical effects of the smoke.
Paul J. DeMott, Jessica A. Mirrielees, Sarah Suda Petters, Daniel J. Cziczo, Markus D. Petters, Heinz G. Bingemer, Thomas C. J. Hill, Karl Froyd, Sarvesh Garimella, A. Gannet Hallar, Ezra J. T. Levin, Ian B. McCubbin, Anne E. Perring, Christopher N. Rapp, Thea Schiebel, Jann Schrod, Kaitlyn J. Suski, Daniel Weber, Martin J. Wolf, Maria Zawadowicz, Jake Zenker, Ottmar Möhler, and Sarah D. Brooks
Atmos. Meas. Tech., 18, 639–672, https://doi.org/10.5194/amt-18-639-2025, https://doi.org/10.5194/amt-18-639-2025, 2025
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The Fifth International Ice Nucleation Workshop Phase 3 (FIN-03) compared the ambient atmospheric performance of ice-nucleating particle (INP) measuring systems and explored general methods for discerning atmospheric INP compositions. Mirroring laboratory results, INP concentrations agreed within 5–10 factors. Measurements of total aerosol properties and investigations of INP compositions supported a dominant role of soil and plant organic aerosol elements as INPs during the study.
Gregory P. Schill, Karl D. Froyd, Daniel M. Murphy, Christina J. Williamson, Charles A. Brock, Tomás Sherwen, Mat J. Evans, Eric A. Ray, Eric C. Apel, Rebecca S. Hornbrook, Alan J. Hills, Jeff Peischl, Thomas B. Ryerson, Chelsea R. Thompson, Ilann Bourgeois, Donald R. Blake, Joshua P. DiGangi, and Glenn S. Diskin
Atmos. Chem. Phys., 25, 45–71, https://doi.org/10.5194/acp-25-45-2025, https://doi.org/10.5194/acp-25-45-2025, 2025
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Using single-particle mass spectrometry, we show that trace concentrations of bromine and iodine are ubiquitous in remote tropospheric aerosol and suggest that aerosols are an important part of the global reactive iodine budget. Comparisons to a global climate model with detailed iodine chemistry are favorable in the background atmosphere; however, the model cannot replicate our measurements near the ocean surface, in biomass burning plumes, and in the stratosphere.
Xiaoli Shen, David M. Bell, Hugh Coe, Naruki Hiranuma, Fabian Mahrt, Nicholas A. Marsden, Claudia Mohr, Daniel M. Murphy, Harald Saathoff, Johannes Schneider, Jacqueline Wilson, Maria A. Zawadowicz, Alla Zelenyuk, Paul J. DeMott, Ottmar Möhler, and Daniel J. Cziczo
Atmos. Chem. Phys., 24, 10869–10891, https://doi.org/10.5194/acp-24-10869-2024, https://doi.org/10.5194/acp-24-10869-2024, 2024
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Single-particle mass spectrometry (SPMS) is commonly used to measure the chemical composition and mixing state of aerosol particles. Intercomparison of SPMS instruments was conducted. All instruments reported similar size ranges and common spectral features. The instrument-specific detection efficiency was found to be more dependent on particle size than type. All differentiated secondary organic aerosol, soot, and soil dust but had difficulties differentiating among minerals and dusts.
Maya Abou-Ghanem, Daniel M. Murphy, Gregory P. Schill, Michael J. Lawler, and Karl D. Froyd
Atmos. Chem. Phys., 24, 8263–8275, https://doi.org/10.5194/acp-24-8263-2024, https://doi.org/10.5194/acp-24-8263-2024, 2024
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Using particle analysis by laser mass spectrometry, we examine vanadium-containing ship exhaust particles measured on NASA's DC-8 during the Atmospheric Tomography Mission (ATom). Our results reveal ship exhaust particles are sufficiently widespread in the marine atmosphere and experience atmospheric aging. Finally, we use laboratory calibrations to determine the vanadium, sulfate, and organic single-particle mass fractions of vanadium-containing ship exhaust particles.
Christina V. Brodowsky, Timofei Sukhodolov, Gabriel Chiodo, Valentina Aquila, Slimane Bekki, Sandip S. Dhomse, Michael Höpfner, Anton Laakso, Graham W. Mann, Ulrike Niemeier, Giovanni Pitari, Ilaria Quaglia, Eugene Rozanov, Anja Schmidt, Takashi Sekiya, Simone Tilmes, Claudia Timmreck, Sandro Vattioni, Daniele Visioni, Pengfei Yu, Yunqian Zhu, and Thomas Peter
Atmos. Chem. Phys., 24, 5513–5548, https://doi.org/10.5194/acp-24-5513-2024, https://doi.org/10.5194/acp-24-5513-2024, 2024
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The aerosol layer is an essential part of the climate system. We characterize the sulfur budget in a volcanically quiescent (background) setting, with a special focus on the sulfate aerosol layer using, for the first time, a multi-model approach. The aim is to identify weak points in the representation of the atmospheric sulfur budget in an intercomparison of nine state-of-the-art coupled global circulation models.
Huisheng Bian, Mian Chin, Peter R. Colarco, Eric C. Apel, Donald R. Blake, Karl Froyd, Rebecca S. Hornbrook, Jose Jimenez, Pedro Campuzano Jost, Michael Lawler, Mingxu Liu, Marianne Tronstad Lund, Hitoshi Matsui, Benjamin A. Nault, Joyce E. Penner, Andrew W. Rollins, Gregory Schill, Ragnhild B. Skeie, Hailong Wang, Lu Xu, Kai Zhang, and Jialei Zhu
Atmos. Chem. Phys., 24, 1717–1741, https://doi.org/10.5194/acp-24-1717-2024, https://doi.org/10.5194/acp-24-1717-2024, 2024
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This work studies sulfur in the remote troposphere at global and seasonal scales using aircraft measurements and multi-model simulations. The goal is to understand the sulfur cycle over remote oceans, spread of model simulations, and observation–model discrepancies. Such an understanding and comparison with real observations are crucial to narrow down the uncertainties in model sulfur simulations and improve understanding of the sulfur cycle in atmospheric air quality, climate, and ecosystems.
Simone Tilmes, Michael J. Mills, Yunqian Zhu, Charles G. Bardeen, Francis Vitt, Pengfei Yu, David Fillmore, Xiaohong Liu, Brian Toon, and Terry Deshler
Geosci. Model Dev., 16, 6087–6125, https://doi.org/10.5194/gmd-16-6087-2023, https://doi.org/10.5194/gmd-16-6087-2023, 2023
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We implemented an alternative aerosol scheme in the high- and low-top model versions of the Community Earth System Model Version 2 (CESM2) with a more detailed description of tropospheric and stratospheric aerosol size distributions than the existing aerosol model. This development enables the comparison of different aerosol schemes with different complexity in the same model framework. It identifies improvements compared to a range of observations in both the troposphere and stratosphere.
Meloë S. F. Kacenelenbogen, Qian Tan, Sharon P. Burton, Otto P. Hasekamp, Karl D. Froyd, Yohei Shinozuka, Andreas J. Beyersdorf, Luke Ziemba, Kenneth L. Thornhill, Jack E. Dibb, Taylor Shingler, Armin Sorooshian, Reed W. Espinosa, Vanderlei Martins, Jose L. Jimenez, Pedro Campuzano-Jost, Joshua P. Schwarz, Matthew S. Johnson, Jens Redemann, and Gregory L. Schuster
Atmos. Chem. Phys., 22, 3713–3742, https://doi.org/10.5194/acp-22-3713-2022, https://doi.org/10.5194/acp-22-3713-2022, 2022
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The impact of aerosols on Earth's radiation budget and human health is important and strongly depends on their composition. One desire of our scientific community is to derive the composition of the aerosol from satellite sensors. However, satellites observe aerosol optical properties (and not aerosol composition) based on remote sensing instrumentation. This study assesses how much aerosol optical properties can tell us about aerosol composition.
Adam T. Ahern, Frank Erdesz, Nicholas L. Wagner, Charles A. Brock, Ming Lyu, Kyra Slovacek, Richard H. Moore, Elizabeth B. Wiggins, and Daniel M. Murphy
Atmos. Meas. Tech., 15, 1093–1105, https://doi.org/10.5194/amt-15-1093-2022, https://doi.org/10.5194/amt-15-1093-2022, 2022
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Particles in the atmosphere play a significant role in climate change by scattering light back into space, reducing the amount of energy available to be absorbed by greenhouse gases. We built a new instrument to measure what direction light is scattered by particles, e.g., wildfire smoke. This is important because, depending on the angle of the sun, some particles scatter light into space (cooling the planet), but some light is also scattered towards the Earth (not cooling the planet).
Li Zhang, Georg A. Grell, Stuart A. McKeen, Ravan Ahmadov, Karl D. Froyd, and Daniel Murphy
Geosci. Model Dev., 15, 467–491, https://doi.org/10.5194/gmd-15-467-2022, https://doi.org/10.5194/gmd-15-467-2022, 2022
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Applying the chemistry package from WRF-Chem into the Flow-following finite-volume Icosahedra Model, we essentially make it possible to explore the importance of different levels of complexity in gas and aerosol chemistry, as well as in physics parameterizations, for the interaction processes in global modeling systems. The model performance validated by the Atmospheric Tomography Mission aircraft measurements in summer 2016 shows good performance in capturing the aerosol and gas-phase tracers.
Charles A. Brock, Karl D. Froyd, Maximilian Dollner, Christina J. Williamson, Gregory Schill, Daniel M. Murphy, Nicholas J. Wagner, Agnieszka Kupc, Jose L. Jimenez, Pedro Campuzano-Jost, Benjamin A. Nault, Jason C. Schroder, Douglas A. Day, Derek J. Price, Bernadett Weinzierl, Joshua P. Schwarz, Joseph M. Katich, Siyuan Wang, Linghan Zeng, Rodney Weber, Jack Dibb, Eric Scheuer, Glenn S. Diskin, Joshua P. DiGangi, ThaoPaul Bui, Jonathan M. Dean-Day, Chelsea R. Thompson, Jeff Peischl, Thomas B. Ryerson, Ilann Bourgeois, Bruce C. Daube, Róisín Commane, and Steven C. Wofsy
Atmos. Chem. Phys., 21, 15023–15063, https://doi.org/10.5194/acp-21-15023-2021, https://doi.org/10.5194/acp-21-15023-2021, 2021
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The Atmospheric Tomography Mission was an airborne study that mapped the chemical composition of the remote atmosphere. From this, we developed a comprehensive description of aerosol properties that provides a unique, global-scale dataset against which models can be compared. The data show the polluted nature of the remote atmosphere in the Northern Hemisphere and quantify the contributions of sea salt, dust, soot, biomass burning particles, and pollution particles to the haziness of the sky.
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Short summary
Parameterizations of dust lifting and microphysical properties of dust in climate models are still subject to large uncertainty. Here we use a sectional aerosol climate model to investigate the global vertical distributions of the dust. Constrained by a suite of observations, the model suggests that, although North African dust dominates global dust mass loading at the surface, the relative contribution of Asian dust increases with altitude and becomes dominant in the upper troposphere.
Parameterizations of dust lifting and microphysical properties of dust in climate models are...
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