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
Related authors
No articles found.
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
Short summary
Short summary
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.
Gregory P. Schill, Karl D. Froyd, Daniel M. Murphy, Christina J. Williamson, Charles Brock, Tomás Sherwen, Mat J. Evans, Eric A. Ray, Eric C. Apel, Rebecca S. Hornbrook, Alan J. Hills, Jeff Peischl, Tomas B. Ryerson, Chelsea R. Thompson, Ilann Bourgeois, Donald R. Blake, Joshua P. DiGangi, and Glenn S. Diskin
EGUsphere, https://doi.org/10.5194/egusphere-2024-1399, https://doi.org/10.5194/egusphere-2024-1399, 2024
Short summary
Short summary
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.
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
Short summary
Short summary
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.
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
EGUsphere, https://doi.org/10.5194/egusphere-2024-928, https://doi.org/10.5194/egusphere-2024-928, 2024
Short summary
Short summary
Single particle mass spectrometer (SPMS) is commonly used to measure chemical composition and mixing state of aerosol particles. Intercomparison of SPMSs 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 instruments differentiated secondary organic aerosol, soot, and soil dust, but had difficulties differentiating among specific minerals and dusts.
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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.
Christina J. Williamson, Agnieszka Kupc, Andrew Rollins, Jan Kazil, Karl D. Froyd, Eric A. Ray, Daniel M. Murphy, Gregory P. Schill, Jeff Peischl, Chelsea Thompson, Ilann Bourgeois, Thomas B. Ryerson, Glenn S. Diskin, Joshua P. DiGangi, Donald R. Blake, Thao Paul V. Bui, Maximilian Dollner, Bernadett Weinzierl, and Charles A. Brock
Atmos. Chem. Phys., 21, 9065–9088, https://doi.org/10.5194/acp-21-9065-2021, https://doi.org/10.5194/acp-21-9065-2021, 2021
Short summary
Short summary
Aerosols in the stratosphere influence climate by scattering and absorbing sunlight and through chemical reactions occurring on the particles’ surfaces. We observed more nucleation mode aerosols (small aerosols, with diameters below 12 nm) in the mid- and high-latitude lowermost stratosphere (8–13 km) in the Northern Hemisphere (NH) than in the Southern Hemisphere. The most likely cause of this is aircraft emissions, which are concentrated in the NH at similar altitudes to our observations.
Daniel M. Murphy, Karl D. Froyd, Ilann Bourgeois, Charles A. Brock, Agnieszka Kupc, Jeff Peischl, Gregory P. Schill, Chelsea R. Thompson, Christina J. Williamson, and Pengfei Yu
Atmos. Chem. Phys., 21, 8915–8932, https://doi.org/10.5194/acp-21-8915-2021, https://doi.org/10.5194/acp-21-8915-2021, 2021
Short summary
Short summary
New measurements in the lower stratosphere highlight differences between particles that originated in the troposphere or the stratosphere. The stratospheric-origin particles have relatively large radiative effects because they are at nearly the optimum diameter for light scattering. The tropospheric particles contribute significantly to surface area. These and other chemical and physical properties are then extended to study the implications if material were to be added to the stratosphere.
Agnieszka Kupc, Christina J. Williamson, Anna L. Hodshire, Jan Kazil, Eric Ray, T. Paul Bui, Maximilian Dollner, Karl D. Froyd, Kathryn McKain, Andrew Rollins, Gregory P. Schill, Alexander Thames, Bernadett B. Weinzierl, Jeffrey R. Pierce, and Charles A. Brock
Atmos. Chem. Phys., 20, 15037–15060, https://doi.org/10.5194/acp-20-15037-2020, https://doi.org/10.5194/acp-20-15037-2020, 2020
Short summary
Short summary
Tropical upper troposphere over the Atlantic and Pacific oceans is a major source region of new particles. These particles are associated with the outflow from deep convection. We investigate the processes that govern the formation of these particles and their initial growth and show that none of the formation schemes commonly used in global models are consistent with observations. Using newer schemes indicates that organic compounds are likely important as nucleating and initial growth agents.
Alma Hodzic, Pedro Campuzano-Jost, Huisheng Bian, Mian Chin, Peter R. Colarco, Douglas A. Day, Karl D. Froyd, Bernd Heinold, Duseong S. Jo, Joseph M. Katich, John K. Kodros, Benjamin A. Nault, Jeffrey R. Pierce, Eric Ray, Jacob Schacht, Gregory P. Schill, Jason C. Schroder, Joshua P. Schwarz, Donna T. Sueper, Ina Tegen, Simone Tilmes, Kostas Tsigaridis, Pengfei Yu, and Jose L. Jimenez
Atmos. Chem. Phys., 20, 4607–4635, https://doi.org/10.5194/acp-20-4607-2020, https://doi.org/10.5194/acp-20-4607-2020, 2020
Short summary
Short summary
Organic aerosol (OA) is a key source of uncertainty in aerosol climate effects. We present the first pole-to-pole OA characterization during the NASA Atmospheric Tomography aircraft mission. OA has a strong seasonal and zonal variability, with the highest levels in summer and over fire-influenced regions and the lowest ones in the southern high latitudes. We show that global models predict the OA distribution well but not the relative contribution of OA emissions vs. chemical production.
Nicholas A. Davis, Sean M. Davis, Robert W. Portmann, Eric Ray, Karen H. Rosenlof, and Pengfei Yu
Geosci. Model Dev., 13, 717–734, https://doi.org/10.5194/gmd-13-717-2020, https://doi.org/10.5194/gmd-13-717-2020, 2020
Short summary
Short summary
Large-scale waves drive upward motion in the tropical stratosphere, with major impacts on stratospheric chemistry and climate. However, some of the modeling methods which attempt to simulate the past evolution of the stratosphere do not seem to be able to recreate important trends. We believe this is due to disagreements between the basic climate of the model and observations, but if the method is constructed more carefully, the disagreement becomes smaller and the trends become more realistic.
Karl D. Froyd, Daniel M. Murphy, Charles A. Brock, Pedro Campuzano-Jost, Jack E. Dibb, Jose-Luis Jimenez, Agnieszka Kupc, Ann M. Middlebrook, Gregory P. Schill, Kenneth L. Thornhill, Christina J. Williamson, James C. Wilson, and Luke D. Ziemba
Atmos. Meas. Tech., 12, 6209–6239, https://doi.org/10.5194/amt-12-6209-2019, https://doi.org/10.5194/amt-12-6209-2019, 2019
Short summary
Short summary
Single-particle mass spectrometer (SPMS) instruments characterize the composition of individual aerosol particles in real time. We present a new method that combines SPMS composition with independently measured particle size distributions to determine absolute number, surface area, volume, and mass concentrations of mineral dust, biomass burning, sea salt, and other climate-relevant atmospheric particle types, with a fast time response applicable to aircraft sampling.
Maria A. Zawadowicz, Karl D. Froyd, Anne E. Perring, Daniel M. Murphy, Dominick V. Spracklen, Colette L. Heald, Peter R. Buseck, and Daniel J. Cziczo
Atmos. Chem. Phys., 19, 13859–13870, https://doi.org/10.5194/acp-19-13859-2019, https://doi.org/10.5194/acp-19-13859-2019, 2019
Short summary
Short summary
We report measurements of small particles of biological origin (for example, fragments of bacteria, pollen, or fungal spores) in the atmosphere over the continental United States. We use a recently developed identification technique based on airborne mass spectrometry in conjunction with an extensive aircraft dataset. We show that biological particles are present at altitudes up to 10 km and we quantify typical concentrations.
Huisheng Bian, Karl Froyd, Daniel M. Murphy, Jack Dibb, Anton Darmenov, Mian Chin, Peter R. Colarco, Arlindo da Silva, Tom L. Kucsera, Gregory Schill, Hongbin Yu, Paul Bui, Maximilian Dollner, Bernadett Weinzierl, and Alexander Smirnov
Atmos. Chem. Phys., 19, 10773–10785, https://doi.org/10.5194/acp-19-10773-2019, https://doi.org/10.5194/acp-19-10773-2019, 2019
Short summary
Short summary
We address the GEOS-GOCART sea salt simulations constrained by NASA EVS ATom measurements, as well as those by MODIS and the AERONET MAN. The study covers remote regions over the Pacific, Atlantic, and Southern oceans from near the surface to ~ 12 km altitude and covers both summer and winter seasons. Important sea salt fields, e.g., mass mixing ratio, vertical distribution, size distribution, and marine aerosol AOD, as well as their relationship to relative humidity and emissions, are examined.
Charles A. Brock, Christina Williamson, Agnieszka Kupc, Karl D. Froyd, Frank Erdesz, Nicholas Wagner, Matthews Richardson, Joshua P. Schwarz, Ru-Shan Gao, Joseph M. Katich, Pedro Campuzano-Jost, Benjamin A. Nault, Jason C. Schroder, Jose L. Jimenez, Bernadett Weinzierl, Maximilian Dollner, ThaoPaul Bui, and Daniel M. Murphy
Atmos. Meas. Tech., 12, 3081–3099, https://doi.org/10.5194/amt-12-3081-2019, https://doi.org/10.5194/amt-12-3081-2019, 2019
Short summary
Short summary
From 2016 to 2018 a NASA aircraft profiled the atmosphere from 180 m to ~12 km from the Arctic to the Antarctic over both the Pacific and Atlantic oceans. This program, ATom, sought to sample atmospheric chemical composition to compare with global climate models. We describe the how measurements of particulate matter were made during ATom, and show that the instrument performance was excellent. Data from this project can be used with confidence to evaluate models and compare with satellites.
Daniel M. Murphy, Karl D. Froyd, Huisheng Bian, Charles A. Brock, Jack E. Dibb, Joshua P. DiGangi, Glenn Diskin, Maximillian Dollner, Agnieszka Kupc, Eric M. Scheuer, Gregory P. Schill, Bernadett Weinzierl, Christina J. Williamson, and Pengfei Yu
Atmos. Chem. Phys., 19, 4093–4104, https://doi.org/10.5194/acp-19-4093-2019, https://doi.org/10.5194/acp-19-4093-2019, 2019
Short summary
Short summary
We present the first data on the concentration of sea-salt aerosol throughout most of the depth of the troposphere and a wide range of latitudes. Sea-salt concentrations in the upper troposphere are very small. This puts stringent limits on how sea-salt aerosol affects halogen and nitric acid chemistry there. With a widely distributed source, sea-salt aerosol provides an excellent test of wet scavenging and vertical transport of aerosols in chemical transport models.
Katherine M. Manfred, Rebecca A. Washenfelder, Nicholas L. Wagner, Gabriela Adler, Frank Erdesz, Caroline C. Womack, Kara D. Lamb, Joshua P. Schwarz, Alessandro Franchin, Vanessa Selimovic, Robert J. Yokelson, and Daniel M. Murphy
Atmos. Chem. Phys., 18, 1879–1894, https://doi.org/10.5194/acp-18-1879-2018, https://doi.org/10.5194/acp-18-1879-2018, 2018
Short summary
Short summary
In this study, we use a new laser imaging nephelometer to measure the bulk aerosol scattering phase function for biomass burning aerosol from controlled fires. By comparing measurements to models for spherical and fractal particles, we demonstrate that the dominant morphology varies by fuel type. This instrument has unique capabilities to directly measure how morphology affects optical properties, and can be used in the future for important validations of remote sensing retrievals.
William T. Ball, Justin Alsing, Daniel J. Mortlock, Johannes Staehelin, Joanna D. Haigh, Thomas Peter, Fiona Tummon, Rene Stübi, Andrea Stenke, John Anderson, Adam Bourassa, Sean M. Davis, Doug Degenstein, Stacey Frith, Lucien Froidevaux, Chris Roth, Viktoria Sofieva, Ray Wang, Jeannette Wild, Pengfei Yu, Jerald R. Ziemke, and Eugene V. Rozanov
Atmos. Chem. Phys., 18, 1379–1394, https://doi.org/10.5194/acp-18-1379-2018, https://doi.org/10.5194/acp-18-1379-2018, 2018
Short summary
Short summary
Using a robust analysis, with artefact-corrected ozone data, we confirm upper stratospheric ozone is recovering following the Montreal Protocol, but that lower stratospheric ozone (50° S–50° N) has continued to decrease since 1998, and the ozone layer as a whole (60° S–60° N) may be lower today than in 1998. No change in total column ozone may be due to increasing tropospheric ozone. State-of-the-art models do not reproduce lower stratospheric ozone decreases.
Jin Liao, Charles A. Brock, Daniel M. Murphy, Donna T. Sueper, André Welti, and Ann M. Middlebrook
Atmos. Meas. Tech., 10, 3801–3820, https://doi.org/10.5194/amt-10-3801-2017, https://doi.org/10.5194/amt-10-3801-2017, 2017
Short summary
Short summary
The Aerodyne aerosol mass spectrometer (AMS) has emerged as a widely used method for measuring the real-time, submicron, nonrefractory aerosol composition. A large uncertainty in accurate measurements with the AMS (the collection efficiency due to particle bounce) is evaluated in this paper using in situ measurements of particle light scattering. Current calculations of the collection efficiency reasonably predict this effect in acidic environments, resulting in more confidence for AMS results.
Maria A. Zawadowicz, Karl D. Froyd, Daniel M. Murphy, and Daniel J. Cziczo
Atmos. Chem. Phys., 17, 7193–7212, https://doi.org/10.5194/acp-17-7193-2017, https://doi.org/10.5194/acp-17-7193-2017, 2017
Short summary
Short summary
This paper reports the results of laboratory and field measurements of primary biological aerosol particles using single-particle mass spectrometry (SPMS). Identification of biological particles using SPMS can be challenging, as their mass spectra can present features similar to phosphorus-containing minerals and combustion by-products. Using a large database of laboratory measurements, a criterion for the identification of biological particles has been developed.
Hongyu Guo, Jiumeng Liu, Karl D. Froyd, James M. Roberts, Patrick R. Veres, Patrick L. Hayes, Jose L. Jimenez, Athanasios Nenes, and Rodney J. Weber
Atmos. Chem. Phys., 17, 5703–5719, https://doi.org/10.5194/acp-17-5703-2017, https://doi.org/10.5194/acp-17-5703-2017, 2017
Short summary
Short summary
Fine particle pH is linked to many environmental impacts by affecting particle concentration and composition. Predicted Pasadena, CA (CalNex campaign), PM1 pH is 1.9 and PM2.5 pH 2.7, the latter higher due to sea salts. The model predicted gas–particle partitionings of HNO3–NO3−, NH3–NH4+, and HCl–Cl− are in good agreement, verifying the model predictions. A summary of contrasting locations in the US and eastern Mediterranean shows fine particles are generally highly acidic, with pH below 3.
Charles A. Brock, Nicholas L. Wagner, Bruce E. Anderson, Alexis R. Attwood, Andreas Beyersdorf, Pedro Campuzano-Jost, Annmarie G. Carlton, Douglas A. Day, Glenn S. Diskin, Timothy D. Gordon, Jose L. Jimenez, Daniel A. Lack, Jin Liao, Milos Z. Markovic, Ann M. Middlebrook, Nga L. Ng, Anne E. Perring, Matthews S. Richardson, Joshua P. Schwarz, Rebecca A. Washenfelder, Andre Welti, Lu Xu, Luke D. Ziemba, and Daniel M. Murphy
Atmos. Chem. Phys., 16, 4987–5007, https://doi.org/10.5194/acp-16-4987-2016, https://doi.org/10.5194/acp-16-4987-2016, 2016
Short summary
Short summary
Microscopic pollution particles make the atmosphere look hazy and also cool the earth by sending sunlight back to space. When the air is moist, these particles swell with water and scatter even more sunlight. We showed that particles formed from organic material – which dominates particulate pollution in the southeastern U.S. – does not take up water very effectively, toward the low end of most previous studies. We also found a better way to mathematically describe this swelling process.
Charles A. Brock, Nicholas L. Wagner, Bruce E. Anderson, Andreas Beyersdorf, Pedro Campuzano-Jost, Douglas A. Day, Glenn S. Diskin, Timothy D. Gordon, Jose L. Jimenez, Daniel A. Lack, Jin Liao, Milos Z. Markovic, Ann M. Middlebrook, Anne E. Perring, Matthews S. Richardson, Joshua P. Schwarz, Andre Welti, Luke D. Ziemba, and Daniel M. Murphy
Atmos. Chem. Phys., 16, 5009–5019, https://doi.org/10.5194/acp-16-5009-2016, https://doi.org/10.5194/acp-16-5009-2016, 2016
Short summary
Short summary
Two research aircraft made dozens of vertical profiles over rural areas in the southeastern US in summer 2013. These measurements show that, in addition to how much pollution was present and how moist the atmosphere was, the size of the pollutant particles affected how much sunlight was reflected back to space. These measurements will help climate modelers determine which characteristics of pollution are important to predict with accuracy.
E. A. Marais, D. J. Jacob, J. L. Jimenez, P. Campuzano-Jost, D. A. Day, W. Hu, J. Krechmer, L. Zhu, P. S. Kim, C. C. Miller, J. A. Fisher, K. Travis, K. Yu, T. F. Hanisco, G. M. Wolfe, H. L. Arkinson, H. O. T. Pye, K. D. Froyd, J. Liao, and V. F. McNeill
Atmos. Chem. Phys., 16, 1603–1618, https://doi.org/10.5194/acp-16-1603-2016, https://doi.org/10.5194/acp-16-1603-2016, 2016
Short summary
Short summary
Isoprene secondary organic aerosol (SOA) is a dominant aerosol component in the southeast US, but models routinely underestimate isoprene SOA with traditional schemes based on chamber studies operated under conditions not representative of isoprene-emitting forests. We develop a new irreversible uptake mechanism to reproduce isoprene SOA yields (3.3 %) and composition, and find a factor of 2 co-benefit of SO2 emission controls on reducing sulfate and organic aerosol in the southeast US.
P. S. Kim, D. J. Jacob, J. A. Fisher, K. Travis, K. Yu, L. Zhu, R. M. Yantosca, M. P. Sulprizio, J. L. Jimenez, P. Campuzano-Jost, K. D. Froyd, J. Liao, J. W. Hair, M. A. Fenn, C. F. Butler, N. L. Wagner, T. D. Gordon, A. Welti, P. O. Wennberg, J. D. Crounse, J. M. St. Clair, A. P. Teng, D. B. Millet, J. P. Schwarz, M. Z. Markovic, and A. E. Perring
Atmos. Chem. Phys., 15, 10411–10433, https://doi.org/10.5194/acp-15-10411-2015, https://doi.org/10.5194/acp-15-10411-2015, 2015
N. L. Wagner, C. A. Brock, W. M. Angevine, A. Beyersdorf, P. Campuzano-Jost, D. Day, J. A. de Gouw, G. S. Diskin, T. D. Gordon, M. G. Graus, J. S. Holloway, G. Huey, J. L. Jimenez, D. A. Lack, J. Liao, X. Liu, M. Z. Markovic, A. M. Middlebrook, T. Mikoviny, J. Peischl, A. E. Perring, M. S. Richardson, T. B. Ryerson, J. P. Schwarz, C. Warneke, A. Welti, A. Wisthaler, L. D. Ziemba, and D. M. Murphy
Atmos. Chem. Phys., 15, 7085–7102, https://doi.org/10.5194/acp-15-7085-2015, https://doi.org/10.5194/acp-15-7085-2015, 2015
Short summary
Short summary
This paper investigates the summertime vertical profile of aerosol over the southeastern US using in situ measurements collected from aircraft. We use a vertical mixing model and measurements of CO to predict the vertical profile of aerosol that we would expect from vertical mixing alone and compare with the observed aerosol profile. We found a modest enhancement of aerosol in the cloudy transition layer during shallow cumulus convection and attribute the enhancement to local aerosol formation.
D. M. Murphy
Atmos. Chem. Phys., 14, 13013–13022, https://doi.org/10.5194/acp-14-13013-2014, https://doi.org/10.5194/acp-14-13013-2014, 2014
Short summary
Short summary
The properties of cirrus clouds depend on the rate at which air cools as the cloud forms. Small-scale motions in the atmosphere have high rates of cooling. This usually leads to very small ice crystals. However, a few random cooling fluctuations will produce only a few ice crystals. This paper shows that these events are important even if they are rare: they lead to particles that sediment and influence a lot of air. The results show dehydration is less sensitive to details of ice nucleation.
Related subject area
Subject: Aerosols | Research Activity: Atmospheric Modelling and Data Analysis | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Analysis of secondary inorganic aerosols over the greater Athens area using the EPISODE–CityChem source dispersion and photochemistry model
Global estimates of ambient reactive nitrogen components during 2000–2100 based on the multi-stage model
The role of naphthalene and its derivatives in the formation of secondary organic aerosol in the Yangtze River Delta region, China
Unveiling the optimal regression model for source apportionment of the oxidative potential of PM10
Investigating the contribution of grown new particles to cloud condensation nuclei with largely varying preexisting particles – Part 2: Modeling chemical drivers and 3-D new particle formation occurrence
Technical note: Influence of different averaging metrics and temporal resolutions on the aerosol pH calculated by thermodynamic modeling
Dual roles of the inorganic aqueous phase on secondary organic aerosol growth from benzene and phenol
Global source apportionment of aerosols into major emission regions and sectors over 1850–2017
Modeling atmospheric brown carbon in the GISS ModelE Earth system model
Observation-constrained kinetic modeling of isoprene SOA formation in the atmosphere
Significant impact of urban tree biogenic emissions on air quality estimated by a bottom-up inventory and chemistry transport modeling
Secondary organic aerosols derived from intermediate-volatility n-alkanes adopt low-viscous phase state
Cooling radiative forcing effect enhancement of atmospheric amines-mineral particle caused by heterogeneous uptake and oxidation
Modeling the drivers of fine PM pollution over Central Europe: impacts and contributions of emissions from different sources
Reaction of SO3 with H2SO4 and its implications for aerosol particle formation in the gas phase and at the air–water interface
Weakened aerosol–radiation interaction exacerbating ozone pollution in eastern China since China's clean air actions
Uncertainties from biomass burning aerosols in air quality models obscure public health impacts in Southeast Asia
The Co-benefits of a Low-Carbon Future on Air Quality in Europe
Oxidative potential apportionment of atmospheric PM1: a new approach combining high-sensitive online analysers for chemical composition and offline OP measurement technique
Observed and CMIP6 model simulated organic aerosol response to drought in the contiguous United States during summertime
Aqueous-phase chemistry of glyoxal with multifunctional reduced nitrogen compounds: a potential missing route for secondary brown carbon
An updated modeling framework to simulate Los Angeles air quality – Part 1: Model development, evaluation, and source apportionment
Frequent haze events associated with transport and stagnation over the corridor between the North China Plain and Yangtze River Delta
Evaluation of WRF-Chem-simulated meteorology and aerosols over northern India during the severe pollution episode of 2016
How well are aerosol–cloud interactions represented in climate models? – Part 1: Understanding the sulfate aerosol production from the 2014–15 Holuhraun eruption
pH regulates the formation of organosulfates and inorganic sulfate from organic peroxide reaction with dissolved SO2 in aquatic media
Technical note: Accurate, reliable, and high-resolution air quality predictions by improving the Copernicus Atmosphere Monitoring Service using a novel statistical post-processing method
Contribution of intermediate-volatility organic compounds from on-road transport to secondary organic aerosol levels in Europe
Source-resolved atmospheric metal emissions, concentrations, and their deposition fluxes into the East Asian Seas
Development of an integrated model framework for multi-air-pollutant exposure assessments in high-density cities
CAMx–UNIPAR simulation of secondary organic aerosol mass formed from multiphase reactions of hydrocarbons under the Central Valley urban atmospheres of California
Impact of urbanization on fine particulate matter concentrations over central Europe
Measurement report: Assessing the impacts of emission uncertainty on aerosol optical properties and radiative forcing from biomass burning in peninsular Southeast Asia
The Emissions Model Intercomparison Project (Emissions-MIP): quantifying model sensitivity to emission characteristics
Dynamics-based estimates of decline trend with fine temporal variations in China's PM2.5 emissions
Effects of simulated secondary organic aerosol water on PM1 levels and composition over the US
Reactive organic carbon air emissions from mobile sources in the United States
Development and evaluation of processes affecting simulation of diel fine particulate matter variation in the GEOS-Chem model
Substantially positive contributions of new particle formation to cloud condensation nuclei under low supersaturation in China based on numerical model improvements
Evolution of atmospheric age of particles and its implications for the formation of a severe haze event in eastern China
A multimodel evaluation of the potential impact of shipping on particle species in the Mediterranean Sea
How does tropospheric VOC chemistry affect climate? An investigation of preindustrial control simulations using the Community Earth System Model version 2
Anthropogenic amplification of biogenic secondary organic aerosol production
A dynamic parameterization of sulfuric acid–dimethylamine nucleation and its application in three-dimensional modeling
Modeling dust mineralogical composition: sensitivity to soil mineralogy atlases and their expected climate impacts
Assessment of the impacts of cloud chemistry on surface SO2 and sulfate levels in typical regions of China
Impact of Landes forest fires on air quality in France during the 2022 summer
Global nitrogen and sulfur deposition mapping using a measurement–model fusion approach
Comprehensive simulations of new particle formation events in Beijing with a cluster dynamics–multicomponent sectional model
Implications of differences between recent anthropogenic aerosol emission inventories for diagnosed AOD and radiative forcing from 1990 to 2019
Stelios Myriokefalitakis, Matthias Karl, Kim A. Weiss, Dimitris Karagiannis, Eleni Athanasopoulou, Anastasia Kakouri, Aikaterini Bougiatioti, Eleni Liakakou, Iasonas Stavroulas, Georgios Papangelis, Georgios Grivas, Despina Paraskevopoulou, Orestis Speyer, Nikolaos Mihalopoulos, and Evangelos Gerasopoulos
Atmos. Chem. Phys., 24, 7815–7835, https://doi.org/10.5194/acp-24-7815-2024, https://doi.org/10.5194/acp-24-7815-2024, 2024
Short summary
Short summary
A state-of-the-art thermodynamic model has been coupled with the city-scale chemistry transport model EPISODE–CityChem to investigate the equilibrium between the inorganic gas and aerosol phases over the greater Athens area, Greece. The simulations indicate that the formation of nitrates in an urban environment is significantly affected by local nitrogen oxide emissions, as well as ambient temperature, relative humidity, photochemical activity, and the presence of non-volatile cations.
Rui Li, Yining Gao, Lijia Zhang, Yubing Shen, Tianzhao Xu, Wenwen Sun, and Gehui Wang
Atmos. Chem. Phys., 24, 7623–7636, https://doi.org/10.5194/acp-24-7623-2024, https://doi.org/10.5194/acp-24-7623-2024, 2024
Short summary
Short summary
A three-stage model was developed to obtain the global maps of reactive nitrogen components during 2000–2100. The results implied that cross-validation R2 values of four species showed satisfactory performance (R2 > 0.55). Most reactive nitrogen components, except NH3, in China showed increases during 2000–2013. In the future scenarios, SSP3-7.0 (traditional-energy scenario) and SSP1-2.6 (carbon neutrality scenario) showed the highest and lowest reactive nitrogen component concentrations.
Fei Ye, Jingyi Li, Yaqin Gao, Hongli Wang, Jingyu An, Cheng Huang, Song Guo, Keding Lu, Kangjia Gong, Haowen Zhang, Momei Qin, and Jianlin Hu
Atmos. Chem. Phys., 24, 7467–7479, https://doi.org/10.5194/acp-24-7467-2024, https://doi.org/10.5194/acp-24-7467-2024, 2024
Short summary
Short summary
Naphthalene (Nap) and methylnaphthalene (MN) are key precursors of secondary organic aerosol (SOA), yet their sources and sinks are often inadequately represented in air quality models. In this study, we incorporated detailed emissions, gas-phase chemistry, and SOA parameterization of Nap and MN into CMAQ to address this issue. The findings revealed remarkably high SOA formation potentials for these compounds despite their low emissions in the Yangtze River Delta region during summer.
Vy Dinh Ngoc Thuy, Jean-Luc Jaffrezo, Ian Hough, Pamela A. Dominutti, Guillaume Salque Moreton, Grégory Gille, Florie Francony, Arabelle Patron-Anquez, Olivier Favez, and Gaëlle Uzu
Atmos. Chem. Phys., 24, 7261–7282, https://doi.org/10.5194/acp-24-7261-2024, https://doi.org/10.5194/acp-24-7261-2024, 2024
Short summary
Short summary
The capacity of particulate matter (PM) to generate reactive oxygen species in vivo is represented by oxidative potential (OP). This study focuses on finding the appropriate model to evaluate the oxidative character of PM sources in six sites using the PM sources and OP. Eight regression techniques are introduced to assess the OP of PM. The study highlights the importance of selecting a model according to the input data characteristics and establishes some recommendations for the procedure.
Ming Chu, Xing Wei, Shangfei Hai, Yang Gao, Huiwang Gao, Yujiao Zhu, Biwu Chu, Nan Ma, Juan Hong, Yele Sun, and Xiaohong Yao
Atmos. Chem. Phys., 24, 6769–6786, https://doi.org/10.5194/acp-24-6769-2024, https://doi.org/10.5194/acp-24-6769-2024, 2024
Short summary
Short summary
We used a 20-bin WRF-Chem model to simulate NPF events in the NCP during a three-week observational period in the summer of 2019. The model was able to reproduce the observations during June 29–July 6, which was characterized by a high frequency of NPF occurrence.
Haoqi Wang, Xiao Tian, Wanting Zhao, Jiacheng Li, Haoyu Yu, Yinchang Feng, and Shaojie Song
Atmos. Chem. Phys., 24, 6583–6592, https://doi.org/10.5194/acp-24-6583-2024, https://doi.org/10.5194/acp-24-6583-2024, 2024
Short summary
Short summary
pH is a key property of ambient aerosols, which affect many atmospheric processes. As aerosol pH is a non-conservative parameter, diverse averaging metrics and temporal resolutions may influence the pH values calculated by thermodynamic models. This technical note seeks to quantitatively evaluate the average pH using varied metrics and resolutions. The ultimate goal is to establish standardized reporting practices in future research endeavors.
Jiwon Choi, Myoseon Jang, and Spencer Blau
Atmos. Chem. Phys., 24, 6567–6582, https://doi.org/10.5194/acp-24-6567-2024, https://doi.org/10.5194/acp-24-6567-2024, 2024
Short summary
Short summary
Persistent phenoxy radical (PPR), formed by phenol gas oxidation and its aqueous reaction, catalytically destroys O3 and retards secondary organic aerosol (SOA) growth. Explicit gas mechanisms including the formation of PPR and low-volatility products from the oxidation of phenol or benzene are applied to the UNIPAR model to predict SOA mass via multiphase reactions of precursors. Aqueous reactions of reactive organics increase SOA mass but retard SOA growth via heterogeneously formed PPR.
Yang Yang, Shaoxuan Mou, Hailong Wang, Pinya Wang, Baojie Li, and Hong Liao
Atmos. Chem. Phys., 24, 6509–6523, https://doi.org/10.5194/acp-24-6509-2024, https://doi.org/10.5194/acp-24-6509-2024, 2024
Short summary
Short summary
The variations in anthropogenic aerosol concentrations and source contributions and their subsequent radiative impact in major emission regions during historical periods are quantified based on an aerosol-tagging system in E3SMv1. Due to the industrial development and implementation of economic policies, sources of anthropogenic aerosols show different variations, which has important implications for pollution prevention and control measures and decision-making for global collaboration.
Maegan A. DeLessio, Kostas Tsigaridis, Susanne E. Bauer, Jacek Chowdhary, and Gregory L. Schuster
Atmos. Chem. Phys., 24, 6275–6304, https://doi.org/10.5194/acp-24-6275-2024, https://doi.org/10.5194/acp-24-6275-2024, 2024
Short summary
Short summary
This study presents the first explicit representation of brown carbon aerosols in the GISS ModelE Earth system model (ESM). Model sensitivity to a range of brown carbon parameters and model performance compared to AERONET and MODIS retrievals of total aerosol properties were assessed. A summary of best practices for incorporating brown carbon into ModelE is also included.
Chuanyang Shen, Xiaoyan Yang, Joel Thornton, John Shilling, Chenyang Bi, Gabriel Isaacman-VanWertz, and Haofei Zhang
Atmos. Chem. Phys., 24, 6153–6175, https://doi.org/10.5194/acp-24-6153-2024, https://doi.org/10.5194/acp-24-6153-2024, 2024
Short summary
Short summary
In this work, a condensed multiphase isoprene oxidation mechanism was developed to simulate isoprene SOA formation from chamber and field studies. Our results show that the measured isoprene SOA mass concentrations can be reasonably reproduced. The simulation results indicate that multifunctional low-volatility products contribute significantly to total isoprene SOA. Our findings emphasize that the pathways to produce these low-volatility species should be considered in models.
Alice Maison, Lya Lugon, Soo-Jin Park, Alexia Baudic, Christopher Cantrell, Florian Couvidat, Barbara D'Anna, Claudia Di Biagio, Aline Gratien, Valérie Gros, Carmen Kalalian, Julien Kammer, Vincent Michoud, Jean-Eudes Petit, Marwa Shahin, Leila Simon, Myrto Valari, Jérémy Vigneron, Andrée Tuzet, and Karine Sartelet
Atmos. Chem. Phys., 24, 6011–6046, https://doi.org/10.5194/acp-24-6011-2024, https://doi.org/10.5194/acp-24-6011-2024, 2024
Short summary
Short summary
This study presents the development of a bottom-up inventory of urban tree biogenic emissions. Emissions are computed for each tree based on their location and characteristics and are integrated in the regional air quality model WRF-CHIMERE. The impact of these biogenic emissions on air quality is quantified for June–July 2022. Over Paris city, urban trees increase the concentrations of particulate organic matter by 4.6 %, of PM2.5 by 0.6 %, and of ozone by 1.0 % on average over 2 months.
Tommaso Galeazzo, Bernard Aumont, Marie Camredon, Richard Valorso, Yong B. Lim, Paul J. Ziemann, and Manabu Shiraiwa
Atmos. Chem. Phys., 24, 5549–5565, https://doi.org/10.5194/acp-24-5549-2024, https://doi.org/10.5194/acp-24-5549-2024, 2024
Short summary
Short summary
Secondary organic aerosol (SOA) derived from n-alkanes is a major component of anthropogenic particulate matter. We provide an analysis of n-alkane SOA by chemistry modeling, machine learning, and laboratory experiments, showing that n-alkane SOA adopts low-viscous semi-solid or liquid states. Our results indicate few kinetic limitations of mass accommodation in SOA formation, supporting the application of equilibrium partitioning for simulating n-alkane SOA in large-scale atmospheric models.
Weina Zhang, Jianhua Mai, Zhichao Fan, Yongpeng Ji, Yuemeng Ji, Guiying Li, Yanpeng Gao, and Taicheng An
EGUsphere, https://doi.org/10.5194/egusphere-2024-1048, https://doi.org/10.5194/egusphere-2024-1048, 2024
Short summary
Short summary
Previous studies show distinctive RFE of AOP-mineral mixed particles from individual mineral or AOP particles. This study reveals heterogeneous oxidation causes further RFE enhancement of amine-mineral mixed particle. Note that RFE increment is higher under clean condition than that under polluted condition, which is contributed to high-oxygen-content product. The enhanced RFE of amine-mineral particle caused by heterogenous oxidation is expected to alleviate warming effect.
Lukáš Bartík, Peter Huszár, Jan Karlický, Ondřej Vlček, and Kryštof Eben
Atmos. Chem. Phys., 24, 4347–4387, https://doi.org/10.5194/acp-24-4347-2024, https://doi.org/10.5194/acp-24-4347-2024, 2024
Short summary
Short summary
The presented study deals with the attribution of fine particulate matter (PM2.5) concentrations to anthropogenic emissions over Central Europe using regional-scale models. It calculates the present-day contributions of different emissions sectors to concentrations of PM2.5 and its secondary components. Moreover, the study investigates the effect of chemical nonlinearities by using multiple source attribution methods and secondary organic aerosol calculation methods.
Rui Wang, Yang Cheng, Shasha Chen, Rongrong Li, Yue Hu, Xiaokai Guo, Tianlei Zhang, Fengmin Song, and Hao Li
Atmos. Chem. Phys., 24, 4029–4046, https://doi.org/10.5194/acp-24-4029-2024, https://doi.org/10.5194/acp-24-4029-2024, 2024
Short summary
Short summary
We used quantum chemical calculations, Born–Oppenheimer molecular dynamics simulations, and the ACDC kinetic model to characterize SO3–H2SO4 interaction in the gas phase and at the air–water interface and to study the effect of H2S2O7 on H2SO4–NH3-based clusters. The work expands our understanding of new pathways for the loss of SO3 in acidic polluted areas and helps reveal some missing sources of NPF in metropolitan industrial regions and understand the atmospheric organic–sulfur cycle better.
Hao Yang, Lei Chen, Hong Liao, Jia Zhu, Wenjie Wang, and Xin Li
Atmos. Chem. Phys., 24, 4001–4015, https://doi.org/10.5194/acp-24-4001-2024, https://doi.org/10.5194/acp-24-4001-2024, 2024
Short summary
Short summary
The present study quantifies the response of aerosol–radiation interaction (ARI) to anthropogenic emission reduction from 2013 to 2017, with the main focus on the contribution to changed O3 concentrations over eastern China both in summer and winter using the WRF-Chem model. The weakened ARI due to decreased anthropogenic emission aggravates the summer (winter) O3 pollution by +0.81 ppb (+0.63 ppb), averaged over eastern China.
Margaret R. Marvin, Paul I. Palmer, Fei Yao, Mohd Talib Latif, and Md Firoz Khan
Atmos. Chem. Phys., 24, 3699–3715, https://doi.org/10.5194/acp-24-3699-2024, https://doi.org/10.5194/acp-24-3699-2024, 2024
Short summary
Short summary
We use an atmospheric chemistry model to investigate aerosols emitted from fire activity across Southeast Asia. We find that the limited nature of measurements in this region leads to large uncertainties that significantly hinder the model representation of these aerosols and their impacts on air quality. As a result, the number of monthly attributable deaths is underestimated by as many as 4500, particularly in March at the peak of the mainland burning season.
Connor J. Clayton, Daniel R. Marsh, Steven T. Turnock, Ailish M. Graham, Kirsty J. Pringle, Carly L. Reddington, Rajesh Kumar, and James B. McQuaid
EGUsphere, https://doi.org/10.5194/egusphere-2024-755, https://doi.org/10.5194/egusphere-2024-755, 2024
Short summary
Short summary
We demonstrate that strong climate mitigation could lead to vastly improved air quality in Europe, however, only minimal benefits are seen following the current trajectory of climate mitigation. We use a model that allows us to see where the improvements are greatest (Central Europe) and analyse what sectors are most important for achieving these co-benefits (agriculture/power).
Julie Camman, Benjamin Chazeau, Nicolas Marchand, Amandine Durand, Grégory Gille, Ludovic Lanzi, Jean-Luc Jaffrezo, Henri Wortham, and Gaëlle Uzu
Atmos. Chem. Phys., 24, 3257–3278, https://doi.org/10.5194/acp-24-3257-2024, https://doi.org/10.5194/acp-24-3257-2024, 2024
Short summary
Short summary
Fine particle (PM1) pollution is a major health issue in the city of Marseille, which is subject to numerous pollution sources. Sampling carried out during the summer enabled a fine characterization of the PM1 sources and their oxidative potential, a promising new metric as a proxy for health impact. PM1 came mainly from combustion sources, secondary ammonium sulfate, and organic nitrate, while the oxidative potential of PM1 came from these sources and from resuspended dust in the atmosphere.
Wei Li and Yuxuan Wang
EGUsphere, https://doi.org/10.5194/egusphere-2024-430, https://doi.org/10.5194/egusphere-2024-430, 2024
Short summary
Short summary
This study finds that droughts immensely increased organic aerosol (OA) in the contiguous U.S. during summertime 1998–2019, notably in the Pacific Northwest (PNW) and Southeast (SEUS). The rise of OA in the SEUS is mainly driven by the enhanced formation of isoprene epoxydiols derived secondary organic aerosol due to the increase of isoprene and sulfate, while in the PNW, it is caused by wildfires. Ten climate models captured the OA increase in the PNW, yet greatly underestimated it in the SEUS.
Yuemeng Ji, Zhang Shi, Wenjian Li, Jiaxin Wang, Qiuju Shi, Yixin Li, Lei Gao, Ruize Ma, Weijun Lu, Lulu Xu, Yanpeng Gao, Guiying Li, and Taicheng An
Atmos. Chem. Phys., 24, 3079–3091, https://doi.org/10.5194/acp-24-3079-2024, https://doi.org/10.5194/acp-24-3079-2024, 2024
Short summary
Short summary
The formation mechanisms for secondary brown carbon (SBrC) contributed by multifunctional reduced nitrogen compounds (RNCs) remain unclear. Hence, from combined laboratory experiments and quantum chemical calculations, we investigated the heterogeneous reactions of glyoxal (GL) with multifunctional RNCs, which are driven by four-step indirect nucleophilic addition reactions. Our results show a possible missing source for SBrC formation on urban, regional, and global scales.
Elyse A. Pennington, Yuan Wang, Benjamin C. Schulze, Karl M. Seltzer, Jiani Yang, Bin Zhao, Zhe Jiang, Hongru Shi, Melissa Venecek, Daniel Chau, Benjamin N. Murphy, Christopher M. Kenseth, Ryan X. Ward, Havala O. T. Pye, and John H. Seinfeld
Atmos. Chem. Phys., 24, 2345–2363, https://doi.org/10.5194/acp-24-2345-2024, https://doi.org/10.5194/acp-24-2345-2024, 2024
Short summary
Short summary
To assess the air quality in Los Angeles (LA), we improved the CMAQ model by using dynamic traffic emissions and new secondary organic aerosol schemes to represent volatile chemical products. Source apportionment demonstrates that the urban areas of the LA Basin and vicinity are NOx-saturated, with the largest sensitivity of O3 to changes in volatile organic compounds in the urban core. The improvement and remaining issues shed light on the future direction of the model development.
Feifan Yan, Hang Su, Yafang Cheng, Rujin Huang, Hong Liao, Ting Yang, Yuanyuan Zhu, Shaoqing Zhang, Lifang Sheng, Wenbin Kou, Xinran Zeng, Shengnan Xiang, Xiaohong Yao, Huiwang Gao, and Yang Gao
Atmos. Chem. Phys., 24, 2365–2376, https://doi.org/10.5194/acp-24-2365-2024, https://doi.org/10.5194/acp-24-2365-2024, 2024
Short summary
Short summary
PM2.5 pollution is a major air quality issue deteriorating human health, and previous studies mostly focus on regions like the North China Plain and Yangtze River Delta. However, the characteristics of PM2.5 concentrations between these two regions are studied less often. Focusing on the transport corridor region, we identify an interesting seesaw transport phenomenon with stagnant weather conditions, conducive to PM2.5 accumulation over this region, resulting in large health effects.
Prerita Agarwal, David S. Stevenson, and Mathew R. Heal
Atmos. Chem. Phys., 24, 2239–2266, https://doi.org/10.5194/acp-24-2239-2024, https://doi.org/10.5194/acp-24-2239-2024, 2024
Short summary
Short summary
Air pollution levels across northern India are amongst some of the worst in the world, with episodic and hazardous haze events. Here, the ability of the WRF-Chem model to predict air quality over northern India is assessed against several datasets. Whilst surface wind speed and particle pollution peaks are over- and underestimated, respectively, meteorology and aerosol trends are adequately captured, and we conclude it is suitable for investigating severe particle pollution events.
George Jordan, Florent Malavelle, Ying Chen, Amy Peace, Eliza Duncan, Daniel G. Partridge, Paul Kim, Duncan Watson-Parris, Toshihiko Takemura, David Neubauer, Gunnar Myhre, Ragnhild Skeie, Anton Laakso, and James Haywood
Atmos. Chem. Phys., 24, 1939–1960, https://doi.org/10.5194/acp-24-1939-2024, https://doi.org/10.5194/acp-24-1939-2024, 2024
Short summary
Short summary
The 2014–15 Holuhraun eruption caused a huge aerosol plume in an otherwise unpolluted region, providing a chance to study how aerosol alters cloud properties. This two-part study uses observations and models to quantify this relationship’s impact on the Earth’s energy budget. Part 1 suggests the models capture the observed spatial and chemical evolution of the plume, yet no model plume is exact. Understanding these differences is key for Part 2, where changes to cloud properties are explored.
Lin Du, Xiaofan Lv, Makroni Lily, Kun Li, and Narcisse Tsona Tchinda
Atmos. Chem. Phys., 24, 1841–1853, https://doi.org/10.5194/acp-24-1841-2024, https://doi.org/10.5194/acp-24-1841-2024, 2024
Short summary
Short summary
This study explores the pH effect on the reaction of dissolved SO2 with selected organic peroxides. Results show that the formation of organic and/or inorganic sulfate from these peroxides strongly depends on their electronic structures, and these processes are likely to alter the chemical composition of dissolved organic matter in different ways. The rate constants of these reactions exhibit positive pH and temperature dependencies within pH 1–10 and 240–340 K ranges.
Angelo Riccio and Elena Chianese
Atmos. Chem. Phys., 24, 1673–1689, https://doi.org/10.5194/acp-24-1673-2024, https://doi.org/10.5194/acp-24-1673-2024, 2024
Short summary
Short summary
Starting from the Copernicus Atmosphere Monitoring Service (CAMS), we provided a novel ensemble statistical post-processing approach to improve their air quality predictions. Our approach is able to provide reliable short-term forecasts of pollutant concentrations, which is a key challenge in supporting national authorities in their tasks related to EU Air Quality Directives, such as planning and reporting the state of air quality to the citizens.
Stella E. I. Manavi and Spyros N. Pandis
Atmos. Chem. Phys., 24, 891–909, https://doi.org/10.5194/acp-24-891-2024, https://doi.org/10.5194/acp-24-891-2024, 2024
Short summary
Short summary
Organic vapors of intermediate volatility have often been neglected as sources of atmospheric organic aerosol. In this work we use a new approach for their simulation and quantify the contribution of these compounds emitted by transportation sources (gasoline and diesel vehicles) to particulate matter over Europe. The estimated secondary organic aerosol levels are on average 60 % higher than predicted by previous approaches. However, these estimates are probably lower limits.
Shenglan Jiang, Yan Zhang, Guangyuan Yu, Zimin Han, Junri Zhao, Tianle Zhang, and Mei Zheng
EGUsphere, https://doi.org/10.5194/egusphere-2024-155, https://doi.org/10.5194/egusphere-2024-155, 2024
Short summary
Short summary
This study aims to provide gridded data on sea-wide concentrations, deposition fluxes, and soluble deposition fluxes with detailed source categories of metals by the modified CMAQ model. We developed a monthly emission inventory of six metals – Fe, Al, V, Ni, Zn, and Cu – from land anthropogenic, ship, and dust sources in East Asia in 2017. Our results revealed the contribution of each source to the emissions, concentrations, and deposition fluxes of metals in the East Asian seas.
Zhiyuan Li, Kin-Fai Ho, Harry Fung Lee, and Steve Hung Lam Yim
Atmos. Chem. Phys., 24, 649–661, https://doi.org/10.5194/acp-24-649-2024, https://doi.org/10.5194/acp-24-649-2024, 2024
Short summary
Short summary
This study developed an integrated model framework for accurate multi-air-pollutant exposure assessments in high-density and high-rise cities. Following the proposed integrated model framework, we established multi-air-pollutant exposure models for four major PM10 chemical species as well as four criteria air pollutants with R2 values ranging from 0.73 to 0.93. The proposed framework serves as an important tool for combined exposure assessment in epidemiological studies.
Yujin Jo, Myoseon Jang, Sanghee Han, Azad Madhu, Bonyoung Koo, Yiqin Jia, Zechen Yu, Soontae Kim, and Jinsoo Park
Atmos. Chem. Phys., 24, 487–508, https://doi.org/10.5194/acp-24-487-2024, https://doi.org/10.5194/acp-24-487-2024, 2024
Short summary
Short summary
The CAMx–UNIPAR model simulated the SOA budget formed via multiphase reactions of hydrocarbons and the impact of emissions and climate on SOA characteristics under California’s urban environments during winter 2018. SOA growth was dominated by daytime oxidation of long-chain alkanes and nighttime terpene oxidation with O3 and NO−3 radicals. The spatial distributions of anthropogenic SOA were affected by the northwesterly wind, whereas those of biogenic SOA were insensitive to wind directions.
Peter Huszar, Alvaro Patricio Prieto Perez, Lukáš Bartík, Jan Karlický, and Anahi Villalba-Pradas
Atmos. Chem. Phys., 24, 397–425, https://doi.org/10.5194/acp-24-397-2024, https://doi.org/10.5194/acp-24-397-2024, 2024
Short summary
Short summary
Urbanization transforms rural land into artificial land, while due to human activities, it also introduces a great quantity of emissions. We quantify the impact of urbanization on the final particulate matter pollutant levels by looking not only at these emissions, but also at the way urban land cover influences meteorological conditions, how the removal of pollutants changes due to urban land cover, and how biogenic emissions from vegetation change due to less vegetation in urban areas.
Yinbao Jin, Yiming Liu, Xiao Lu, Xiaoyang Chen, Ao Shen, Haofan Wang, Yinping Cui, Yifei Xu, Siting Li, Jian Liu, Ming Zhang, Yingying Ma, and Qi Fan
Atmos. Chem. Phys., 24, 367–395, https://doi.org/10.5194/acp-24-367-2024, https://doi.org/10.5194/acp-24-367-2024, 2024
Short summary
Short summary
This study aims to address these issues by evaluating eight independent biomass burning (BB) emission inventories (GFED, FINN1.5, FINN2.5 MOS, FINN2.5 MOSVIS, GFAS, FEER, QFED, and IS4FIRES) using the WRF-Chem model and analyzing their impact on aerosol optical properties (AOPs) and direct radiative forcing (DRF) during wildfire events in peninsular Southeast Asia (PSEA) that occurred in March 2019.
Hamza Ahsan, Hailong Wang, Jingbo Wu, Mingxuan Wu, Steven J. Smith, Susanne Bauer, Harrison Suchyta, Dirk Olivié, Gunnar Myhre, Hitoshi Matsui, Huisheng Bian, Jean-François Lamarque, Ken Carslaw, Larry Horowitz, Leighton Regayre, Mian Chin, Michael Schulz, Ragnhild Bieltvedt Skeie, Toshihiko Takemura, and Vaishali Naik
Atmos. Chem. Phys., 23, 14779–14799, https://doi.org/10.5194/acp-23-14779-2023, https://doi.org/10.5194/acp-23-14779-2023, 2023
Short summary
Short summary
We examine the impact of the assumed effective height of SO2 injection, SO2 and BC emission seasonality, and the assumed fraction of SO2 emissions injected as SO4 on climate and chemistry model results. We find that the SO2 injection height has a large impact on surface SO2 concentrations and, in some models, radiative flux. These assumptions are a
hiddensource of inter-model variability and may be leading to bias in some climate model results.
Zhen Peng, Lili Lei, Zhe-Min Tan, Meigen Zhang, Aijun Ding, and Xingxia Kou
Atmos. Chem. Phys., 23, 14505–14520, https://doi.org/10.5194/acp-23-14505-2023, https://doi.org/10.5194/acp-23-14505-2023, 2023
Short summary
Short summary
Annual PM2.5 emissions in China consistently decreased by about 3% to 5% from 2017 to 2020 with spatial variations and seasonal dependencies. High-temporal-resolution and dynamics-based PM2.5 emission estimates provide quantitative diurnal variations for each season. Significant reductions in PM2.5 emissions in the North China Plain and northeast of China in 2020 were caused by COVID-19.
Stylianos Kakavas, Spyros N. Pandis, and Athanasios Nenes
Atmos. Chem. Phys., 23, 13555–13564, https://doi.org/10.5194/acp-23-13555-2023, https://doi.org/10.5194/acp-23-13555-2023, 2023
Short summary
Short summary
Water uptake from organic species in aerosol can affect the partitioning of semi-volatile inorganic compounds but are not considered in global and chemical transport models. We address this with a version of the PM-CAMx model that considers such organic water effects and use it to carry out 1-year aerosol simulations over the continental US. We show that such organic water impacts can increase dry PM1 levels by up to 2 μg m-3 when RH levels and PM1 concentrations are high.
Benjamin N. Murphy, Darrell Sonntag, Karl M. Seltzer, Havala O. T. Pye, Christine Allen, Evan Murray, Claudia Toro, Drew R. Gentner, Cheng Huang, Shantanu Jathar, Li Li, Andrew A. May, and Allen L. Robinson
Atmos. Chem. Phys., 23, 13469–13483, https://doi.org/10.5194/acp-23-13469-2023, https://doi.org/10.5194/acp-23-13469-2023, 2023
Short summary
Short summary
We update methods for calculating organic particle and vapor emissions from mobile sources in the USA. Conventionally, particulate matter (PM) and volatile organic carbon (VOC) are speciated without consideration of primary semivolatile emissions. Our methods integrate state-of-the-science speciation profiles and correct for common artifacts when sampling emissions in a laboratory. We quantify impacts of the emission updates on ambient pollution with the Community Multiscale Air Quality model.
Yanshun Li, Randall V. Martin, Chi Li, Brian L. Boys, Aaron van Donkelaar, Jun Meng, and Jeffrey R. Pierce
Atmos. Chem. Phys., 23, 12525–12543, https://doi.org/10.5194/acp-23-12525-2023, https://doi.org/10.5194/acp-23-12525-2023, 2023
Short summary
Short summary
We developed and evaluated processes affecting within-day (diel) variability in PM2.5 concentrations in a chemical transport model over the contiguous US. Diel variability in PM2.5 for the contiguous US is driven by early-morning accumulation into a shallow mixed layer, decreases from mid-morning through afternoon with mixed-layer growth, increases from mid-afternoon through evening as the mixed-layer collapses, and decreases overnight as emissions decrease.
Chupeng Zhang, Shangfei Hai, Yang Gao, Yuhang Wang, Shaoqing Zhang, Lifang Sheng, Bin Zhao, Shuxiao Wang, Jingkun Jiang, Xin Huang, Xiaojing Shen, Junying Sun, Aura Lupascu, Manish Shrivastava, Jerome D. Fast, Wenxuan Cheng, Xiuwen Guo, Ming Chu, Nan Ma, Juan Hong, Qiaoqiao Wang, Xiaohong Yao, and Huiwang Gao
Atmos. Chem. Phys., 23, 10713–10730, https://doi.org/10.5194/acp-23-10713-2023, https://doi.org/10.5194/acp-23-10713-2023, 2023
Short summary
Short summary
New particle formation is an important source of atmospheric particles, exerting critical influences on global climate. Numerical models are vital tools to understanding atmospheric particle evolution, which, however, suffer from large biases in simulating particle numbers. Here we improve the model chemical processes governing particle sizes and compositions. The improved model reveals substantial contributions of newly formed particles to climate through effects on cloud condensation nuclei.
Xiaodong Xie, Jianlin Hu, Momei Qin, Song Guo, Min Hu, Dongsheng Ji, Hongli Wang, Shengrong Lou, Cheng Huang, Chong Liu, Hongliang Zhang, Qi Ying, Hong Liao, and Yuanhang Zhang
Atmos. Chem. Phys., 23, 10563–10578, https://doi.org/10.5194/acp-23-10563-2023, https://doi.org/10.5194/acp-23-10563-2023, 2023
Short summary
Short summary
The atmospheric age of particles reflects how long particles have been formed and suspended in the atmosphere, which is closely associated with the evolution processes of particles. An analysis of the atmospheric age of PM2.5 provides a unique perspective on the evolution processes of different PM2.5 components. The results also shed lights on how to design effective emission control actions under unfavorable meteorological conditions.
Lea Fink, Matthias Karl, Volker Matthias, Sonia Oppo, Richard Kranenburg, Jeroen Kuenen, Sara Jutterström, Jana Moldanova, Elisa Majamäki, and Jukka-Pekka Jalkanen
Atmos. Chem. Phys., 23, 10163–10189, https://doi.org/10.5194/acp-23-10163-2023, https://doi.org/10.5194/acp-23-10163-2023, 2023
Short summary
Short summary
The Mediterranean Sea is a heavily trafficked shipping area, and air quality monitoring stations in numerous cities along the Mediterranean coast have detected high levels of air pollutants originating from shipping emissions. The current study investigates how existing restrictions on shipping-related emissions to the atmosphere ensure compliance with legislation. Focus was laid on fine particles and particle species, which were simulated with five different chemical transport models.
Noah A. Stanton and Neil F. Tandon
Atmos. Chem. Phys., 23, 9191–9216, https://doi.org/10.5194/acp-23-9191-2023, https://doi.org/10.5194/acp-23-9191-2023, 2023
Short summary
Short summary
Chemistry in Earth’s atmosphere has a potentially strong but very uncertain impact on climate. Past attempts to fully model chemistry in Earth’s troposphere (the lowest layer of the atmosphere) typically simplified the representation of Earth’s surface, which in turn limited the ability to simulate changes in climate. The cutting-edge model that we use in this study does not require such simplification, and we use it to examine the climate effects of chemical interactions in the troposphere.
Yiqi Zheng, Larry W. Horowitz, Raymond Menzel, David J. Paynter, Vaishali Naik, Jingyi Li, and Jingqiu Mao
Atmos. Chem. Phys., 23, 8993–9007, https://doi.org/10.5194/acp-23-8993-2023, https://doi.org/10.5194/acp-23-8993-2023, 2023
Short summary
Short summary
Biogenic secondary organic aerosols (SOAs) account for a large fraction of fine aerosol at the global scale. Using long-term measurements and a climate model, we investigate anthropogenic impacts on biogenic SOA at both decadal and centennial timescales. Results show that despite reductions in biogenic precursor emissions, SOA has been strongly amplified by anthropogenic emissions since the preindustrial era and exerts a cooling radiative forcing.
Yuyang Li, Jiewen Shen, Bin Zhao, Runlong Cai, Shuxiao Wang, Yang Gao, Manish Shrivastava, Da Gao, Jun Zheng, Markku Kulmala, and Jingkun Jiang
Atmos. Chem. Phys., 23, 8789–8804, https://doi.org/10.5194/acp-23-8789-2023, https://doi.org/10.5194/acp-23-8789-2023, 2023
Short summary
Short summary
We set up a new parameterization for 1.4 nm particle formation rates from sulfuric acid–dimethylamine (SA–DMA) nucleation, fully including the effects of coagulation scavenging and cluster stability. Incorporating the new parameterization into 3-D chemical transport models, we achieved better consistencies between simulation results and observation data. This new parameterization provides new insights into atmospheric nucleation simulations and its effects on atmospheric pollution or health.
María Gonçalves Ageitos, Vincenzo Obiso, Ron L. Miller, Oriol Jorba, Martina Klose, Matt Dawson, Yves Balkanski, Jan Perlwitz, Sara Basart, Enza Di Tomaso, Jerónimo Escribano, Francesca Macchia, Gilbert Montané, Natalie M. Mahowald, Robert O. Green, David R. Thompson, and Carlos Pérez García-Pando
Atmos. Chem. Phys., 23, 8623–8657, https://doi.org/10.5194/acp-23-8623-2023, https://doi.org/10.5194/acp-23-8623-2023, 2023
Short summary
Short summary
Dust aerosols affect our climate differently depending on their mineral composition. We include dust mineralogy in an atmospheric model considering two existing soil maps, which still have large associated uncertainties. The soil data and the distribution of the minerals in different aerosol sizes are key to our model performance. We find significant regional variations in climate-relevant variables, which supports including mineralogy in our current models and the need for improved soil maps.
Jianyan Lu, Sunling Gong, Jian Zhang, Jianmin Chen, Lei Zhang, and Chunhong Zhou
Atmos. Chem. Phys., 23, 8021–8037, https://doi.org/10.5194/acp-23-8021-2023, https://doi.org/10.5194/acp-23-8021-2023, 2023
Short summary
Short summary
WRF/CUACE was used to assess the cloud chemistry contribution in China. Firstly, the CUACE cloud chemistry scheme was found to reproduce well the cloud processing and consumption of H2O2, O3, and SO2, as well as the increase of sulfate. Secondly, during cloud availability in December under a heavy pollution episode, sulfate production increased 60–95 % and SO2 was reduced by over 80 %. This study provides a way to analyze the phenomenon of overestimation of SO2 in many chemical transport models.
Laurent Menut, Arineh Cholakian, Guillaume Siour, Rémy Lapere, Romain Pennel, Sylvain Mailler, and Bertrand Bessagnet
Atmos. Chem. Phys., 23, 7281–7296, https://doi.org/10.5194/acp-23-7281-2023, https://doi.org/10.5194/acp-23-7281-2023, 2023
Short summary
Short summary
This study is about the wildfires occurring in France during the summer 2022. We study the forest fires that took place in the Landes during the summer of 2022. We show the direct impact of these fires on the air quality, especially downstream of the smoke plume towards the Paris region. We quantify the impact of these fires on the pollutants peak concentrations and the possible exceedance of thresholds.
Hannah J. Rubin, Joshua S. Fu, Frank Dentener, Rui Li, Kan Huang, and Hongbo Fu
Atmos. Chem. Phys., 23, 7091–7102, https://doi.org/10.5194/acp-23-7091-2023, https://doi.org/10.5194/acp-23-7091-2023, 2023
Short summary
Short summary
We update the 2010 global deposition budget for nitrogen (N) and sulfur (S) with new regional wet deposition measurements, improving the ensemble results of 11 global chemistry transport models from HTAP II. Our study demonstrates that a global measurement–model fusion approach can substantially improve N and S deposition model estimates at a regional scale and represents a step forward toward the WMO goal of global fusion products for accurately mapping harmful air pollution.
Chenxi Li, Yuyang Li, Xiaoxiao Li, Runlong Cai, Yaxin Fan, Xiaohui Qiao, Rujing Yin, Chao Yan, Yishuo Guo, Yongchun Liu, Jun Zheng, Veli-Matti Kerminen, Markku Kulmala, Huayun Xiao, and Jingkun Jiang
Atmos. Chem. Phys., 23, 6879–6896, https://doi.org/10.5194/acp-23-6879-2023, https://doi.org/10.5194/acp-23-6879-2023, 2023
Short summary
Short summary
New particle formation and growth in polluted environments are not fully understood despite intensive research. We applied a cluster dynamics–multicomponent sectional model to simulate the new particle formation events observed in Beijing, China. The simulation approximately captures how the events evolve. Further diagnosis shows that the oxygenated organic molecules may have been under-detected, and modulating their abundance leads to significantly improved simulation–observation agreement.
Marianne Tronstad Lund, Gunnar Myhre, Ragnhild Bieltvedt Skeie, Bjørn Hallvard Samset, and Zbigniew Klimont
Atmos. Chem. Phys., 23, 6647–6662, https://doi.org/10.5194/acp-23-6647-2023, https://doi.org/10.5194/acp-23-6647-2023, 2023
Short summary
Short summary
Here we show that differences, in magnitude and trend, between recent global anthropogenic emission inventories have a notable influence on simulated regional abundances of anthropogenic aerosol over the 1990–2019 period. This, in turn, affects estimates of radiative forcing. Our findings form a basis for comparing existing and upcoming studies on anthropogenic aerosols using different emission inventories.
Cited articles
Adebiyi, A. A. and Kok, J. F.: Climate models miss most of the coarse dust
in the atmosphere, Sci. Adv., 6, eaaz9507, https://doi.org/10.1126/sciadv.aaz9507, 2020.
Andreae, M. O.: Climatic effects of changing atmospheric aerosol levels,
World Surv. Climatol., 16, 347–398, 1995.
Andreae, M. O., Charlson, R. J., Bruynseels, F., Storms, H., Van Grieken,
R., and Maenhaut, W.: Internal mixture of sea salt, silicates, and excess
sulfate in marine aerosols, Science, 232, 1620–1623, 1986.
Appel, O., Köllner, F., Dragoneas, A., Hünig, A., Molleker, S., Schlager, H., Mahnke, C., Weigel, R., Port, M., Schulz, C., Drewnick, F., Vogel, B., Stroh, F., and Borrmann, S.: Chemical analysis of the Asian Tropopause Aerosol Layer (ATAL) with emphasis on secondary aerosol particles using aircraft based in situ aerosol mass spectrometry, Atmos. Chem. Phys. Discuss. [preprint], https://doi.org/10.5194/acp-2022-92, in review, 2022.
Arimoto, R., Duce, R. A., Ray, B. J., Ellis, W. G., Cullen, J. D., and Merrill, J. T.: Trace-Elements in the Atmosphere over the North-Atlantic, J. Geophys. Res.-Atmos., 100, 1199–1213, 1995.
Arimoto, R., Duce, R. A., Savoie, D. L., Prospero, J. M., Talbot, R.,
Cullen, J. D., Tomza, U., Lewis, N. F., and Ray, B. J.: Relationships among
aerosol constituents from Asia and the North Pacific during PEM-West A, J.
Geophys. Res.-Atmos., 101, 2011–2023,
https://doi.org/10.1029/95JD01071, 1996.
Balkanski, Y., Schulz, M., Claquin, T., and Guibert, S.: Reevaluation of Mineral aerosol radiative forcings suggests a better agreement with satellite and AERONET data, Atmos. Chem. Phys., 7, 81–95, https://doi.org/10.5194/acp-7-81-2007, 2007.
Bardeen, C., Toon, O., Jensen, E., Marsh, D., and Harvey, V.: Numerical
simulations of the three-dimensional distribution of meteoric dust in the
mesosphere and upper stratosphere, J. Geophys. Res.-Atmos., 113, D17202, https://doi.org/10.1029/2007jd009515, 2008.
Bory, A. J. M., Biscaye, P. E., Svensson, A., and Grousset, F. E.: Seasonal variability in the
origin of recent atmospheric mineral dust at NorthGRIP, Greenland,
Earth Planet. Sc. Lett., 196, 123–134,
https://doi.org/10.1016/S0012-821X(01)00609-4, 2002.
Bory, A. J. M., Biscaye, P. E., and Grousset, F. E.: Two distinct seasonal Asian source
regions for mineral dust deposited in Greenland (NorthGRIP), Geophys. Res.
Lett., 30, 1167,
https://doi.org/10.1029/2002GL016446, 2003.
Bossolasco, A., Jegou, F., Sellitto, P., Berthet, G., Kloss, C., and Legras, B.: Global modeling studies of composition and decadal trends of the Asian Tropopause Aerosol Layer, Atmos. Chem. Phys., 21, 2745–2764, https://doi.org/10.5194/acp-21-2745-2021, 2021.
Bourgeois, I., Peischl, J., Thompson, C. R., Aikin, K. C., Campos, T., Clark, H., Commane, R., Daube, B., Diskin, G. W., Elkins, J. W., Gao, R.-S., Gaudel, A., Hintsa, E. J., Johnson, B. J., Kivi, R., McKain, K., Moore, F. L., Parrish, D. D., Querel, R., Ray, E., Sánchez, R., Sweeney, C., Tarasick, D. W., Thompson, A. M., Thouret, V., Witte, J. C., Wofsy, S. C., and Ryerson, T. B.: Global-scale distribution of ozone in the remote troposphere from the ATom and HIPPO airborne field missions, Atmos. Chem. Phys., 20, 10611–10635, https://doi.org/10.5194/acp-20-10611-2020, 2020.
Bourgeois, Q., Ekman, A. M. L., and Krejci, R.: Aerosol transport over the
Andes from the Amazon Basin to the remote Pacific Ocean: A multiyear CALIOP
assessment, J. Geophys. Res.-Atmos., 120, 8411–8425, https://doi.org/10.1002/2015jd023254, 2015.
Brock, C. A., Williamson, C., Kupc, A., Froyd, K. D., Erdesz, F., Wagner, N., Richardson, M., Schwarz, J. P., Gao, R.-S., Katich, J. M., Campuzano-Jost, P., Nault, B. A., Schroder, J. C., Jimenez, J. L., Weinzierl, B., Dollner, M., Bui, T., and Murphy, D. M.: Aerosol size distributions during the Atmospheric Tomography Mission (ATom): methods, uncertainties, and data products, Atmos. Meas. Tech., 12, 3081–3099, https://doi.org/10.5194/amt-12-3081-2019, 2019.
Caffrey, P. F., Fromm, M. D., and Kablick, G. P.: WRF-Chem Simulation of an
East Asian Dust-Infused Baroclinic Storm (DIBS), J. Geophys. Res.-Atmos.,
123, 6880–6895, https://doi.org/10.1029/2017jd027848, 2018.
Chin, M., Diehl, T., Ginoux, P., and Malm, W.: Intercontinental transport of pollution and dust aerosols: implications for regional air quality, Atmos. Chem. Phys., 7, 5501–5517, https://doi.org/10.5194/acp-7-5501-2007, 2007.
Colarco, P. R., Toon, O. B., Reid, J. S., Livingston, J. M., Russell, P. B., Redemann, J., Schmid, B., Maring, H. B., Savoie, D., Welton, E. J., Campbell, J. R., Holben, B. N., and Levy, R.: North African dust transport to the
Caribbean during PRIDE: 2. Transport, vertical profiles, and deposition in
simulations of in situ and remote sensing observations, J. Geophys. Res.-Atmos., 108, 8590, https://doi.org/10.1029/2002JD002659, 2003.
Cziczo, D. J., Froyd, K. D., Hoose, C., Jensen, E. J., Diao, M. H., Zondlo,
M. A., Smith, J. B., Twohy, C. H., and Murphy, D. M.: Clarifying the
Dominant Sources and Mechanisms of Cirrus Cloud Formation, Science, 340,
1320–1324, https://doi.org/10.1126/science.1234145, 2013.
d'Almeida, G. A.: A model for Saharan dust transport, J. Appl. Meteorol.
Climatol., 25, 903–916, 1986.
Di Biagio, C., Formenti, P., Balkanski, Y., Caponi, L., Cazaunau, M., Pangui, E., Journet, E., Nowak, S., Andreae, M. O., Kandler, K., Saeed, T., Piketh, S., Seibert, D., Williams, E., and Doussin, J.-F.: Complex refractive indices and single-scattering albedo of global dust aerosols in the shortwave spectrum and relationship to size and iron content, Atmos. Chem. Phys., 19, 15503–15531, https://doi.org/10.5194/acp-19-15503-2019, 2019.
Froyd, K. D., Murphy, D. M., Lawson, P., Baumgardner, D., and Herman, R. L.: Aerosols that form subvisible cirrus at the tropical tropopause, Atmos. Chem. Phys., 10, 209–218, https://doi.org/10.5194/acp-10-209-2010, 2010.
Froyd, K. D., Murphy, D. M., Brock, C. A., Campuzano-Jost, P., Dibb, J. E., Jimenez, J.-L., Kupc, A., Middlebrook, A. M., Schill, G. P., Thornhill, K. L., Williamson, C. J., Wilson, J. C., and Ziemba, L. D.: A new method to quantify mineral dust and other aerosol species from aircraft platforms using single-particle mass spectrometry, Atmos. Meas. Tech., 12, 6209–6239, https://doi.org/10.5194/amt-12-6209-2019, 2019.
Froyd, K. D., Yu, P. F., Schill, G. P., Brock, C. A., Kupc, A., Williamson,
C. J., Jensen, E. J., Ray, E., Rosenlof, K. H., Bian, H. S., Darmenov, A.
S., Colarco, P. R., Diskin, G. S., Bui, T., and Murphy, D. M.: Dominant role
of mineral dust in cirrus cloud formation revealed by global-scale
measurements, Nat. Geosci., 15, 177–183, https://doi.org/10.1038/s41561-022-00901-w,
2022.
Ginoux, P., Chin, M., Tegen, I., Prospero, J. M., Holben, B., Dubovik, O.,
and Lin, S. J.: Sources and distributions of dust aerosols simulated with
the GOCART model, J. Geophys. Res.-Atmos., 106, 20255–20273, https://doi.org/10.1029/2000jd000053, 2001.
Grell, G. A. and Freitas, S. R.: A scale and aerosol aware stochastic convective parameterization for weather and air quality modeling, Atmos. Chem. Phys., 14, 5233–5250, https://doi.org/10.5194/acp-14-5233-2014, 2014.
Hara, Y., Yumimoto, K., Uno, I., Shimizu, A., Sugimoto, N., Liu, Z., and Winker, D. M.: Asian dust outflow in the PBL and free atmosphere retrieved by NASA CALIPSO and an assimilated dust transport model, Atmos. Chem. Phys., 9, 1227–1239, https://doi.org/10.5194/acp-9-1227-2009, 2009.
Hopfner, M., Ungermann, J., Borrmann, S., Wagner, R., Spang, R., Riese, M.,
Stiller, G., Appel, O., Batenburg, A. M., Bucci, S., Cairo, F., Dragoneas,
A., Friedl-Vallon, F., Hunig, A., Johansson, S., Krasauskas, L., Legras, B.,
Leisner, T., Mahnke, C., Mohler, O., Molleker, S., Muller, R., Neubert, T.,
Orphal, J., Preusse, P., Rex, M., Saathoff, H., Stroh, F., Weigel, R., and
Wohltmann, I.: Ammonium nitrate particles formed in upper troposphere from
ground ammonia sources during Asian monsoons, Nat. Geosci., 12, 608–612,
doi10.1038/s41561-019-0385-8, 2019.
Huneeus, N., Schulz, M., Balkanski, Y., Griesfeller, J., Prospero, J., Kinne, S., Bauer, S., Boucher, O., Chin, M., Dentener, F., Diehl, T., Easter, R., Fillmore, D., Ghan, S., Ginoux, P., Grini, A., Horowitz, L., Koch, D., Krol, M. C., Landing, W., Liu, X., Mahowald, N., Miller, R., Morcrette, J.-J., Myhre, G., Penner, J., Perlwitz, J., Stier, P., Takemura, T., and Zender, C. S.: Global dust model intercomparison in AeroCom phase I, Atmos. Chem. Phys., 11, 7781–7816, https://doi.org/10.5194/acp-11-7781-2011, 2011.
Karyampudi, V. M.: A detailed synoptic-scale study of the structure,
dynamics, and radiative effects of the Saharan air layer over the eastern
tropical Atlantic during the GARP Atlantic tropical experiment, M. S. thesis, Department of Meteorology, The Pennsylvania State University, 136 pp., 1979.
Karyampudi, V. M., Palm, S. P., Reagen, J. A., Fang, H., Grant, W. B., Hoff,
R. M., Moulin, C., Pierce, H. F., Torres, O., Browell, E. V., and Melfi, S.
H.: Validation of the Saharan Dust Plume Conceptual Model Using Lidar,
Meteosat, and ECMWF Data, Bull. Am. Meteorol. Soc., 80, 1045–1076, https://doi.org/10.1175/1520-0477(1999)080<1045:VOTSDP>2.0.CO;2, 1999.
Kawai, K., Kai, K., Jin, Y., Sugimoto, N., and Batdorj, D.: Dust Event in
the Gobi Desert on 22–23 May 2013: Transport of Dust from the Atmospheric
Boundary Layer to the Free Troposphere by a Cold Front, Sola, 11, 156–159,
https://doi.org/10.2151/sola.2015-035, 2015.
Kawai, K., Kai, K., Jin, Y., Sugimoto, N., and Batdorj, D.: Lidar Network
Observation of Dust Layer Development over the Gobi Desert in Association
with a Cold Frontal System on 22–23 May 2013, J. Meteorolog. Soc. Jpn., 96,
255–268, https://doi.org/10.2151/jmsj.2018-023, 2018.
Kok, J. F.: A scaling theory for the size distribution of emitted dust
aerosols suggests climate models underestimate the size of the global dust
cycle, P. Natl. Acad. Sci., 108, 1016–1021, https://doi.org/10.1073/pnas.1014798108, 2011.
Kok, J. F., Adebiyi, A. A., Albani, S., Balkanski, Y., Checa-Garcia, R., Chin, M., Colarco, P. R., Hamilton, D. S., Huang, Y., Ito, A., Klose, M., Li, L., Mahowald, N. M., Miller, R. L., Obiso, V., Pérez García-Pando, C., Rocha-Lima, A., and Wan, J. S.: Contribution of the world's main dust source regions to the global cycle of desert dust, Atmos. Chem. Phys., 21, 8169–8193, https://doi.org/10.5194/acp-21-8169-2021, 2021.
Levin, Z., Ganor, E., and Gladstein, V.: The Effects of Desert Particles
Coated with Sulfate on Rain Formation in the Eastern Mediterranean, J. Appl.
Meteorol. Climatol., 35, 1511–1523, https://doi.org/10.1175/1520-0450(1996)035<1511:TEODPC>2.0.CO;2, 1996.
Lambert, F., Tagliabue, A., Shaffer, G., Lamy, F., Winckler, G., Farias, L.,
Gallardo, L., and De Pol-Holz, R.: Dust fluxes and iron fertilization in
Holocene and Last Glacial Maximum climates, Geophys. Res. Lett., 42,
6014–6023, https://doi.org/10.1002/2015gl064250, 2015.
Ma, J., Brühl, C., He, Q., Steil, B., Karydis, V. A., Klingmüller, K., Tost, H., Chen, B., Jin, Y., Liu, N., Xu, X., Yan, P., Zhou, X., Abdelrahman, K., Pozzer, A., and Lelieveld, J.: Modeling the aerosol chemical composition of the tropopause over the Tibetan Plateau during the Asian summer monsoon, Atmos. Chem. Phys., 19, 11587–11612, https://doi.org/10.5194/acp-19-11587-2019, 2019.
Mahowald, N. M., Baker, A. R., Bergametti, G., Brooks, N., Duce, R. A.,
Jickells, T. D., Kubilay, N., Prospero, J. M., and Tegen, I.: Atmospheric
global dust cycle and iron inputs to the ocean, Global Biogeochem. Cy.,
19, GB4025, https://doi.org/10.1029/2004GB002402, 2005.
Mahowald, N., Jickells, T. D., Baker, A. R., Artaxo, P., BenitezNelson, C.
R., Bergametti, G., Bond, T. C., Chen, Y., Cohen, D. D., Herut, B., Kubilay,
N., Losno, R., Luo, C., Maenhaut, W., McGee, K. A., Okin, G. S., Siefert, R.
L., and Tsukuda, S.:Global distribution of atmospheric phosphorus sources,
concentrations and deposition rates, and anthropogenic impacts, Global
Biogeochem. Cy., 22, GB4026, https://doi.org/10.1029/2008GB003240, 2008.
Mahowald, N. M., Engelstaedter, S., Luo, C., Sealy, A., Artaxo, P.,
Benitez-Nelson, C., Bonnet, S., Chen, Y., Chuang, P. Y., Cohen, D. D.,
Dulac, F., Herut, B., Johansen, A. M., Kubilay, N., Losno, R., Maenhaut, W.,
Paytan, A., Prospero, J. A., Shank, L. M., and Siefert, R. L.: Atmospheric
Iron Deposition: Global Distribution, Variability, and Human Perturbations,
Ann. Rev. Mar. Sci., 1, 245–278, https://doi.org/10.1146/annurev.marine.010908.163727, 2009.
Maloney, C., Toon, B., Bardeen, C., Yu, P. F., Froyd, K., Kay, J., and
Woods, S.: The Balance Between Heterogeneous and Homogeneous Nucleation of
Ice Clouds Using CAM5/CARMA, J. Geophys. Res.-Atmos., 127, e2021JD035540, https://doi.org/10.1029/2021jd035540, 2022.
Marticorena, B. and Bergametti, G.: Modeling the atmospheric dust cycle: 1.
Design of a soil-derived dust emission scheme, J. Geophys. Res.-Atmos., 100,
16415–16430, 1995.
Murphy, D. M., Middlebrook, A. M., and Warshawsky, M.: Cluster analysis of
data from the Particle Analysis by Laser Mass Spectrometry (PALMS)
instrument, Aerosol Sci. Technol., 37, 382–391, https://doi.org/10.1080/02786820300971, 2003.
Murphy, D. M., Cziczo, D. J., Froyd, K. D., Hudson, P. K., Matthew, B. M.,
Middlebrook, A. M., Peltier, R. E., Sullivan, A., Thomson, D. S., and Weber,
R. J.: Single-particle mass spectrometry of tropospheric aerosol particles,
J. Geophys. Res.-Atmos., 111, D23S32, https://doi.org/10.1029/2006jd007340, 2006.
Murphy, D. M., Froyd, K. D., Bourgeois, I., Brock, C. A., Kupc, A., Peischl, J., Schill, G. P., Thompson, C. R., Williamson, C. J., and Yu, P.: Radiative and chemical implications of the size and composition of aerosol particles in the existing or modified global stratosphere, Atmos. Chem. Phys., 21, 8915–8932, https://doi.org/10.5194/acp-21-8915-2021, 2021.
NASA: AERONET Data Download Tool, https://aeronet.gsfc.nasa.gov/cgi-bin/webtool_aod_v3, last access: October 2022.
Nazaryan, H., McCormick, M. P., and Menzel, W. P.: Global characterization
of cirrus clouds using CALIPSO data, J. Geophys. Res.-Atmos., 113, D16211, https://doi.org/10.1029/2007jd009481, 2008.
Prasad, A. K. and Singh, R. P.: Changes in aerosol parameters during major
dust storm events (2001–2005) over the Indo-Gangetic Plains using AERONET
and MODIS data, J. Geophys. Res.-Atmos., 112, D09208, https://doi.org/10.1029/2006jd007778,
2007.
Prospero, J. M., Uematsu, M., and Savoie, D. L.: Mineral aerosol transport to the Pacific Ocean, edited by: Riley, J. P., 187–218, Academic Press, New York, 1989.
Prospero, J. M.: The Atmospheric Transport of Particles to the Ocean, in: Particle Flux in the Ocean, edited by: Ittekkot, V., Schafer, P., Honjo, S., and Depetris, P. J., John Wiley and Sons Ltd., New York, 1996.
Prospero, J. M. and Bonatti, E.: Continental dust in the atmosphere of the
Eastern Equatorial Pacific, J. Geophys. Res., 74, 3362–3371, https://doi.org/10.1029/JC074i013p03362, 1969.
Prospero, J. M., Collard, F.-X., Molinie, J., and Jeannot, A.: Characterizing
the annual cycle of African dust transport to the Caribbean Basin and South
America and its impact on air quality and the environment, Global
Biogeochem. Cy., 29, 757–773, https://doi.org/10.1002/2013GB004802, 2014.
Rosenfeld, D., Rudich, Y., and Lahav, R.: Desert dust suppressing
precipitation: A possible desertification feedback loop, P. Natl. Acad. Sci. USA, 98, 5975–5980,
https://doi.org/10.1073/pnas.101122798, 2001.
Sassen, K., Wang, Z., and Liu, D.: Global distribution of cirrus clouds from
CloudSat/Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations
(CALIPSO) measurements, J. Geophys. Res.-Atmos., 113, D00A12, https://doi.org/10.1029/2008jd009972, 2008.
Satheesh, S. K. and Moorthy, K. K.: Radiative effects of natural aerosols: A
review, Atmos. Environ., 39, 2089–2110, https://doi.org/10.1016/j.atmosenv.2004.12.029,
2005.
Sinyuk, A., Torres, O., and Dubovik, O.: Combined use of satellite and
surface observations to infer the imaginary part of refractive index of
Saharan dust, Geophys. Res. Lett., 30, 1081, https://doi.org/10.1029/2002gl016189, 2003.
Sokolik, I. N. and Toon, O. B.: Direct radiative forcing by anthropogenic
airborne mineral aerosols, Nature, 381, 681–683, https://doi.org/10.1038/381681a0, 1996.
Sokolik, I. N. and Toon, O. B.: Incorporation of mineralogical composition
into models of the radiative properties of mineral aerosol from UV to IR
wavelengths, J. Geophys. Res.-Atmos., 104, 9423–9444, 1999.
Spanu, A., Dollner, M., Gasteiger, J., Bui, T. P., and Weinzierl, B.: Flow-induced errors in airborne in situ measurements of aerosols and clouds, Atmos. Meas. Tech., 13, 1963–1987, https://doi.org/10.5194/amt-13-1963-2020, 2020.
Stith, J. L., Ramanathan, V., Cooper, W. A., Roberts, G. C., DeMott, P. J.,
Carmichael, G., Hatch, C. D., Adhikary, B., Twohy, C. H., Rogers, D. C.,
Baumgardner, D., Prenni, A. J., Campos, T., Gao, R., Anderson, J., and Feng,
Y.: An overview of aircraft observations from the Pacific Dust Experiment
campaign, J. Geophys. Res.-Atmos., 114, D05207, https://doi.org/10.1029/2008jd010924, 2009.
Su, L. and Toon, O. B.: Numerical simulations of Asian dust storms using a
coupled climate-aerosol microphysical model, J. Geophys. Res. Atmos., 114, D14202,
https://doi.org/10.1029/2008jd010956, 2009.
Su, L. and Toon, O. B.: Saharan and Asian dust: similarities and differences determined by CALIPSO, AERONET, and a coupled climate-aerosol microphysical model, Atmos. Chem. Phys., 11, 3263–3280, https://doi.org/10.5194/acp-11-3263-2011, 2011.
Swap, R., Garstang, M., Greco, S., Talbot, R., and Kallberg, P.: Saharan dust in the Amazon Basin,
Tellus B, 44, 133–149, https://doi.org/10.1034/j.1600-0889.1992.t01-1-00005.x, 1992.
Tanaka, T. Y. and Chiba, M.: A numerical study of the contributions of dust
source regions to the global dust budget, Global Planet. Change, 52, 88–104,
https://doi.org/10.1016/j.gloplacha.2006.02.002, 2006.
Tanaka, T. Y., Kurosaki, Y., Chiba, M., Matsumura, T., Nagai, T., Yamazaki,
A., Uchiyama, A., Tsunematsu, N., and Kai, K.: Possible transcontinental
dust transport from North Africa and the Middle East to East Asia, Atmos.
Environ., 39, 3901–3909, https://doi.org/10.1016/j.atmosenv.2005.03.034, 2005.
Tegen, I.: Modeling the mineral dust aerosol cycle in the climate system,
Quaternary Sci. Rev., 22, 1821–1834, https://doi.org/10.1016/s0277-3791(03)00163-x, 2003.
Tegen, I. and Lacis, A. A.: Modeling of particle size distribution and its
influence on the radiative properties of mineral dust aerosol, J. Geophys.
Res.-Atmos., 101, 19237–19244, https://doi.org/10.1029/95jd03610, 1996.
Tegen, I. and Schepanski, K.: The global distribution of mineral dust, IOP
Conf. Ser. Earth Environ. Sci., 7, 012001, https://doi.org/10.1088/1755-1307/7/1/012001, 2009.
Textor, C., Schulz, M., Guibert, S., Kinne, S., Balkanski, Y., Bauer, S., Berntsen, T., Berglen, T., Boucher, O., Chin, M., Dentener, F., Diehl, T., Easter, R., Feichter, H., Fillmore, D., Ghan, S., Ginoux, P., Gong, S., Grini, A., Hendricks, J., Horowitz, L., Huang, P., Isaksen, I., Iversen, I., Kloster, S., Koch, D., Kirkevåg, A., Kristjansson, J. E., Krol, M., Lauer, A., Lamarque, J. F., Liu, X., Montanaro, V., Myhre, G., Penner, J., Pitari, G., Reddy, S., Seland, Ø., Stier, P., Takemura, T., and Tie, X.: Analysis and quantification of the diversities of aerosol life cycles within AeroCom, Atmos. Chem. Phys., 6, 1777–1813, https://doi.org/10.5194/acp-6-1777-2006, 2006.
Thomason, L. W. and Vernier, J.-P.: Improved SAGE II cloud/aerosol categorization and observations of the Asian tropopause aerosol layer: 1989–2005, Atmos. Chem. Phys., 13, 4605–4616, https://doi.org/10.5194/acp-13-4605-2013, 2013.
Toon, O. B., Turco, R. P., Westphal, D., Malone, R., and Liu, M.: A
Multidimensional Model for Aerosols: Description of Computational Analogs,
J. Atmos. Sci., 45, 2123–2144, https://doi.org/10.1175/1520-0469(1988)045<2123:AMMFAD>2.0.CO;2, 1988.
Vernier, J. P., Thomason, L. W., and Kar, J.: CALIPSO detection of an Asian
tropopause aerosol layer, Geophys. Res. Lett., 38, L07804, https://doi.org/10.1029/2010gl046614, 2011.
Vernier, J. P., Fairlie, T. D., Natarajan, M., Wienhold, F. G., Bian, J.,
Martinsson, B. G., Crumeyrolle, S., Thomason, L. W., and Bedka, K. M.:
Increase in upper tropospheric and lower stratospheric aerosol levels and
its potential connection with Asian pollution, J. Geophys. Res.-Atmos., 120,
1608–1619, https://doi.org/10.1002/2014jd022372, 2015.
Vernier, J. P., Fairlie, T. D., Deshler, T., Ratnam, M. V., Gadhavi, H.,
Kumar, B. S., Natarajan, M., Pandit, A. K., Raj, S. T. A., Kumar, A. H.,
Jayaraman, A., Singh, A. K., Rastogi, N., Sinha, P. R., Kumar, S., Tiwari,
S., Wegner, T., Baker, N., Vignelles, D., Stenchikov, G., Shevchenko, I.,
Smith, J., Bedka, K., Kesarkar, A., Singh, V., Bhate, J., Ravikiran, V.,
Rao, M. D., Ravindrababu, S., Patel, A., Vernier, H., Wienhold, F. G., Liu,
H., Knepppp, T. N., Thomason, L., Crawford, J., Ziembmba, L., Moore, J.,
Crumeyrolle, S., Williamson, M., Berthet, G., Jegou, F., and Renard, J. B.:
BATAL The Balloon Measurement Campaigns of the Asian Tropopause Aerosol
Layer, Bull. Am. Meteorol. Soc., 99, 955–973, https://doi.org/10.1175/bams-d-17-0014.1,
2018.
Wang, H., Easter, R. C., Rasch, P. J., Wang, M., Liu, X., Ghan, S. J., Qian, Y., Yoon, J.-H., Ma, P.-L., and Vinoj, V.: Sensitivity of remote aerosol distributions to representation of cloud–aerosol interactions in a global climate model, Geosci. Model Dev., 6, 765–782, https://doi.org/10.5194/gmd-6-765-2013, 2013.
Wang, R., Balkanski, Y., Boucher, O., Bopp, L., Chappell, A., Ciais, P., Hauglustaine, D., Peñuelas, J., and Tao, S.: Sources, transport and deposition of iron in the global atmosphere, Atmos. Chem. Phys., 15, 6247–6270, https://doi.org/10.5194/acp-15-6247-2015, 2015.
Yang, K., Wang, Z. E., Luo, T., Liu, X. H., and Wu, M. X.: Upper troposphere
dust belt formation processes vary seasonally and spatially in the Northern
Hemisphere, Commun. Earth Environ., 3, 24, https://doi.org/10.1038/s43247-022-00353-5, 2022.
Yu, H. B., Chin, M., Winker, D. M., Omar, A. H., Liu, Z. Y., Kittaka, C.,
and Diehl, T.: Global view of aerosol vertical distributions from CALIPSO
lidar measurements and GOCART simulations: Regional and seasonal variations,
J. Geophys. Res.-Atmos., 115, D00H30, https://doi.org/10.1029/2009jd013364, 2010.
Yu, H. B., Chin, M., Bian, H. S., Yuan, T. L., Prospero, J. M., Omar, A. H.,
Remer, L. A., Winker, D. M., Yang, Y. K., Zhang, Y., and Zhang, Z. B.:
Quantification of trans-Atlantic dust transport from seven-year (2007–2013)
record of CALIPSO lidar measurements, Remote Sens. Environ., 159, 232–249,
https://doi.org/10.1016/j.rse.2014.12.010, 2015a.
Yu, H. B., Chin, M., Yuan, T. L., Bian, H. S., Remer, L. A., Prospero, J.
M., Omar, A., Winker, D., Yang, Y. K., Zhang, Y., Zhang, Z. B., and Zhao,
C.: The fertilizing role of African dust in the Amazon rainforest: A first
multiyear assessment based on data from Cloud-Aerosol Lidar and Infrared
Pathfinder Satellite Observations, Geophys. Res. Lett., 42, 1984–1991,
https://doi.org/10.1002/2015gl063040, 2015b.
Yu, P., Rosenlof, K. H., Liu, S., Telg, H., Thornberry, T. D., Rollins, A.
W., Portmann, R. W., Bai, Z., Ray, E. A., Duan, Y., Pan, L. L., Toon, O. B.,
Bian, J., and Gao, R.-S.: Efficient transport of tropospheric aerosol into
the stratosphere via the Asian summer monsoon anticyclone, P. Natl. Acad.
Sci., 114, 6972–6977, https://doi.org/10.1073/pnas.1701170114, 2017.
Yu, P., Lian, S., Zhu, Y., Toon, O. B., Höpfner, M., and Borrmann, S.: Abundant Nitrate and Nitric Acid Aerosol in the Upper troposphere and Lower Stratosphere, Geophys. Res. Lett., 49, e2022GL100258, https://doi.org/10.1029/2022GL100258, 2022.
Yu, P. F., Toon, O. B., Bardeen, C. G., Mills, M. J., Fan, T. Y., English,
J. M., and Neely, R. R.: Evaluations of tropospheric aerosol properties
simulated by the community earth system model with a sectional aerosol
microphysics scheme, J. Adv. Model. Earth Syst., 7, 865–914, https://doi.org/10.1002/2014ms000421, 2015.
Yu, P. F., Froyd, K. D., Portmann, R. W., Toon, O. B., Freitas, S. R.,
Bardeen, C. G., Brock, C., Fan, T. Y., Gao, R. S., Katich, J. M., Kupc, A.,
Liu, S., Maloney, C., Murphy, D. M., Rosenlof, K. H., Schill, G., Schwarz,
J. P., and Williamson, C.: Efficient In-Cloud Removal of Aerosols by Deep
Convection, Geophys. Res. Lett., 46, 1061–1069, https://doi.org/10.1029/2018gl080544,
2019.
Zender, C. S., Miller, R. L. R. L., and Tegen, I.: Quantifying mineral dust mass budgets:Terminology, constraints, and current estimates, Eos Trans. Am. Geophys. Union, 85, 509–512, https://doi.org/10.1029/2004EO480002, 2004.
Zwaaftink, C. D. G., Grythe, H., Skov, H., and Stohl, A.: Substantial
contribution of northern high-latitude sources to mineral dust in the
Arctic, J. Geophys. Res.-Atmos., 121, 13678–13697, https://doi.org/10.1002/2016jd025482, 2016.
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...
Altmetrics
Final-revised paper
Preprint