Articles | Volume 16, issue 2
https://doi.org/10.5194/acp-16-1045-2016
© Author(s) 2016. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
https://doi.org/10.5194/acp-16-1045-2016
© Author(s) 2016. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Research article
| 
29 Jan 2016
Research article |
| 29 Jan 2016
Vertical profiles of optical and microphysical particle properties above the northern Indian Ocean during CARDEX 2012
F. Höpner
CORRESPONDING AUTHOR
Department of Meteorology (MISU) and the Bolin Centre for Climate
Research, Stockholm University, Stockholm, Sweden
F. A.-M. Bender
Department of Meteorology (MISU) and the Bolin Centre for Climate
Research, Stockholm University, Stockholm, Sweden
A. M. L. Ekman
Department of Meteorology (MISU) and the Bolin Centre for Climate
Research, Stockholm University, Stockholm, Sweden
P. S. Praveen
International
Centre for Integrated Mountain Development, Kathmandu, Nepal
C. Bosch
Department of Environmental Science and Analytical Chemistry (ACES)
and the Bolin Centre for Climate Research, Stockholm University, Stockholm,
Sweden
Environment and Energy, Fundació CTM Centre Tecnològic,
Plaça de la Ciència 2, 08243 Manresa, Spain
J. A. Ogren
Earth System Research Laboratory, National Oceanic and
Atmospheric Administration, Boulder, Colorado, USA
A. Andersson
Department of Environmental Science and Analytical Chemistry (ACES)
and the Bolin Centre for Climate Research, Stockholm University, Stockholm,
Sweden
Ö. Gustafsson
Department of Environmental Science and Analytical Chemistry (ACES)
and the Bolin Centre for Climate Research, Stockholm University, Stockholm,
Sweden
V. Ramanathan
Scripps
Institute of Oceanography, University of California, San Diego, California,
USA
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Atmos. Chem. Phys., 24, 13371–13384, https://doi.org/10.5194/acp-24-13371-2024, https://doi.org/10.5194/acp-24-13371-2024, 2024
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Our study explores climate feedbacks, vital for understanding global warming. It links them to shifts in Earth's energy balance at the atmosphere's top due to natural temperature variations. It takes roughly 50 years to establish this connection. Combined satellite observations and reanalysis suggest that Earth cools more than expected under carbon dioxide influence. However, continuous satellite data until at least the mid-2030s are crucial for refining our understanding of climate feedbacks.
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This preprint is open for discussion and under review for Atmospheric Chemistry and Physics (ACP).
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The effects on polar climates of warmer sea surface temperatures and decreasing sea ice cover have been studied using four climate models with identical prescribed changes in sea surface temperatures and sea ice cover. The models predict similar changes in air temperature and precipitation in the polar regions in a warmer climate with less sea ice. However, the models disagree on how the atmospheric circulation, i.e. the large-scale winds, will change with warmer temperatures and less sea ice.
Duncan Watson-Parris, Laura J. Wilcox, Camilla W. Stjern, Robert J. Allen, Geeta Persad, Massimo A. Bollasina, Annica M. L. Ekman, Carley E. Iles, Manoj Joshi, Marianne T. Lund, Daniel McCoy, Daniel Westervelt, Andrew Williams, and Bjørn H. Samset
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In 2020, regulations by the International Maritime Organization aimed to reduce aerosol emissions from ships. These aerosols previously had a cooling effect, which the regulations might reduce, revealing more greenhouse gas warming. Here we find that while there is regional warming, the global 2020–2040 temperature rise is only +0.03°C. This small change is difficult to distinguish from natural climate variability, indicating the regulations have had a limited effect on observed warming to date.
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EGUsphere, https://doi.org/10.5194/egusphere-2024-1891, https://doi.org/10.5194/egusphere-2024-1891, 2024
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The Arctic is experiencing enhanced surface warming. The observed decline in Arctic sea-ice extent is projected to lead to an increase in Arctic shipping activity which may lead to further climatic feedbacks. We investigate, using an atmospheric model and results from marine engine experiments which focused on fuel sulfur content reduction and exhaust wet scrubbing, how ship exhaust particles influence the properties of Arctic clouds. Implications for radiative surface processes are discussed.
Alejandro Baró Pérez, Michael S. Diamond, Frida A.-M. Bender, Abhay Devasthale, Matthias Schwarz, Julien Savre, Juha Tonttila, Harri Kokkola, Hyunho Lee, David Painemal, and Annica M. L. Ekman
Atmos. Chem. Phys., 24, 4591–4610, https://doi.org/10.5194/acp-24-4591-2024, https://doi.org/10.5194/acp-24-4591-2024, 2024
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We use a numerical model to study interactions between humid light-absorbing aerosol plumes, clouds, and radiation over the southeast Atlantic. We find that the warming produced by the aerosols reduces cloud cover, especially in highly polluted situations. Aerosol impacts on drizzle play a minor role. However, aerosol effects on cloud reflectivity and moisture-induced changes in cloud cover dominate the climatic response and lead to an overall cooling by the biomass burning plumes.
Dominic Heslin-Rees, Peter Tunved, Johan Ström, Roxana Cremer, Paul Zieger, Ilona Riipinen, Annica M. L. Ekman, Konstantinos Eleftheriadis, and Radovan Krejci
Atmos. Chem. Phys., 24, 2059–2075, https://doi.org/10.5194/acp-24-2059-2024, https://doi.org/10.5194/acp-24-2059-2024, 2024
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Light-absorbing atmospheric particles (e.g. black carbon – BC) exert a warming effect on the Arctic climate. We show that the amount of particle light absorption decreased from 2002 to 2023. We conclude that in addition to reductions in emissions of BC, wet removal plays a role in the long-term reduction of BC in the Arctic, given the increase in surface precipitation experienced by air masses arriving at the site. The potential impact of biomass burning events is shown to have increased.
Sushant Das, Frida Bender, and Thorsten Mauritsen
EGUsphere, https://doi.org/10.5194/egusphere-2023-1605, https://doi.org/10.5194/egusphere-2023-1605, 2023
Preprint archived
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Quantifying global and Indian precipitation responses to anthropogenic aerosol and CO2 forcings using multiple models is needed for reducing climate uncertainty. The response to global warming from CO2 increases precipitation both globally and over India, whereas the cooling response to sulfate aerosol leads to a reduction in precipitation in both cases. An opposite response to black carbon is noted i.e., a global decrease but an increase of precipitation over India implying changes in dynamics.
Ines Bulatovic, Julien Savre, Michael Tjernström, Caroline Leck, and Annica M. L. Ekman
Atmos. Chem. Phys., 23, 7033–7055, https://doi.org/10.5194/acp-23-7033-2023, https://doi.org/10.5194/acp-23-7033-2023, 2023
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We use numerical modeling with detailed cloud microphysics to investigate a low-altitude cloud system consisting of two cloud layers – a type of cloud situation which was commonly observed during the summer of 2018 in the central Arctic (north of 80° N). The model generally reproduces the observed cloud layers and the thermodynamic structure of the lower atmosphere well. The cloud system is maintained unless there are low aerosol number concentrations or high large-scale wind speeds.
Aiden R. Jönsson and Frida A.-M. Bender
Earth Syst. Dynam., 14, 345–365, https://doi.org/10.5194/esd-14-345-2023, https://doi.org/10.5194/esd-14-345-2023, 2023
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The Earth has nearly the same mean albedo in both hemispheres, a feature not well replicated by climate models. Global warming causes changes in surface and cloud properties that affect albedo and that feed back into the warming. We show that models predict more darkening due to ice loss in the Northern than in the Southern Hemisphere in response to increasing CO2 concentrations. This is, to varying degrees, counteracted by changes in cloud cover, with implications for cloud feedback on climate.
Peter Kuma, Frida A.-M. Bender, Alex Schuddeboom, Adrian J. McDonald, and Øyvind Seland
Atmos. Chem. Phys., 23, 523–549, https://doi.org/10.5194/acp-23-523-2023, https://doi.org/10.5194/acp-23-523-2023, 2023
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We present a machine learning method for determining cloud types in climate model output and satellite observations based on ground observations of cloud genera. We analyse cloud type biases and changes with temperature in climate models and show that the bias is anticorrelated with climate sensitivity. Models simulating decreasing stratiform and increasing cumuliform clouds with increased CO2 concentration tend to have higher climate sensitivity than models simulating the opposite tendencies.
Chaman Gul, Shichang Kang, Siva Praveen Puppala, Xiaokang Wu, Cenlin He, Yangyang Xu, Inka Koch, Sher Muhammad, Rajesh Kumar, and Getachew Dubache
Atmos. Chem. Phys., 22, 8725–8737, https://doi.org/10.5194/acp-22-8725-2022, https://doi.org/10.5194/acp-22-8725-2022, 2022
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This work aims to understand concentrations, spatial variability, and potential source regions of light-absorbing impurities (black carbon aerosols, dust particles, and organic carbon) in the surface snow of central and western Himalayan glaciers and their impact on snow albedo and radiative forcing.
Erik Johansson, Abhay Devasthale, Michael Tjernström, Annica M. L. Ekman, Klaus Wyser, and Tristan L'Ecuyer
Geosci. Model Dev., 14, 4087–4101, https://doi.org/10.5194/gmd-14-4087-2021, https://doi.org/10.5194/gmd-14-4087-2021, 2021
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Understanding the coupling of clouds to large-scale circulation is a grand challenge for the climate community. Cloud radiative heating (CRH) is a key parameter in this coupling and is therefore essential to model realistically. We, therefore, evaluate a climate model against satellite observations. Our findings indicate good agreement in the seasonal pattern of CRH even if the magnitude differs. We also find that increasing the horizontal resolution in the model has little effect on the CRH.
Georgia Sotiropoulou, Luisa Ickes, Athanasios Nenes, and Annica M. L. Ekman
Atmos. Chem. Phys., 21, 9741–9760, https://doi.org/10.5194/acp-21-9741-2021, https://doi.org/10.5194/acp-21-9741-2021, 2021
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Mixed-phase clouds are a large source of uncertainty in projections of the Arctic climate. This is partly due to the poor representation of the cloud ice formation processes. Implementing a parameterization for ice multiplication due to mechanical breakup upon collision of two ice particles in a high-resolution model improves cloud ice phase representation; however, cloud liquid remains overestimated.
Alejandro Baró Pérez, Abhay Devasthale, Frida A.-M. Bender, and Annica M. L. Ekman
Atmos. Chem. Phys., 21, 6053–6077, https://doi.org/10.5194/acp-21-6053-2021, https://doi.org/10.5194/acp-21-6053-2021, 2021
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We study the impacts of above-cloud biomass burning plumes on radiation and clouds over the southeast Atlantic using data derived from satellite observations and data-constrained model simulations. A substantial amount of the aerosol within the plumes is not classified as smoke by the satellite. The atmosphere warms more with increasing smoke aerosol loading. No clear influence of aerosol type, loading, or moisture within the overlying aerosol plumes is detected on the cloud top cooling rates.
Ines Bulatovic, Adele L. Igel, Caroline Leck, Jost Heintzenberg, Ilona Riipinen, and Annica M. L. Ekman
Atmos. Chem. Phys., 21, 3871–3897, https://doi.org/10.5194/acp-21-3871-2021, https://doi.org/10.5194/acp-21-3871-2021, 2021
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We use detailed numerical modelling to show that small aerosol particles (diameters ~25–80 nm; so-called Aitken mode particles) significantly influence low-level cloud properties in the clean summertime high Arctic. The small particles can help sustain clouds when the concentration of larger particles is low (<10–20 cm-3). Measurements from four different observational campaigns in the high Arctic support the modelling results as they indicate that Aitken mode aerosols are frequently activated.
Lena Frey, Frida A.-M. Bender, and Gunilla Svensson
Atmos. Chem. Phys., 21, 577–595, https://doi.org/10.5194/acp-21-577-2021, https://doi.org/10.5194/acp-21-577-2021, 2021
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We investigate the vertical distribution of aerosol in the climate model NorESM1-M in five regions of marine stratocumulus clouds. We thereby analyze the total aerosol extinction to facilitate a comparison with satellite data. We find that the model underestimates aerosol extinction throughout the troposphere, especially elevated aerosol layers. Further, we perform sensitivity experiments to identify the processes most important for vertical aerosol distribution in our model.
Johannes Quaas, Antti Arola, Brian Cairns, Matthew Christensen, Hartwig Deneke, Annica M. L. Ekman, Graham Feingold, Ann Fridlind, Edward Gryspeerdt, Otto Hasekamp, Zhanqing Li, Antti Lipponen, Po-Lun Ma, Johannes Mülmenstädt, Athanasios Nenes, Joyce E. Penner, Daniel Rosenfeld, Roland Schrödner, Kenneth Sinclair, Odran Sourdeval, Philip Stier, Matthias Tesche, Bastiaan van Diedenhoven, and Manfred Wendisch
Atmos. Chem. Phys., 20, 15079–15099, https://doi.org/10.5194/acp-20-15079-2020, https://doi.org/10.5194/acp-20-15079-2020, 2020
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Anthropogenic pollution particles – aerosols – serve as cloud condensation nuclei and thus increase cloud droplet concentration and the clouds' reflection of sunlight (a cooling effect on climate). This Twomey effect is poorly constrained by models and requires satellite data for better quantification. The review summarizes the challenges in properly doing so and outlines avenues for progress towards a better use of aerosol retrievals and better retrievals of droplet concentrations.
Laura J. Wilcox, Zhen Liu, Bjørn H. Samset, Ed Hawkins, Marianne T. Lund, Kalle Nordling, Sabine Undorf, Massimo Bollasina, Annica M. L. Ekman, Srinath Krishnan, Joonas Merikanto, and Andrew G. Turner
Atmos. Chem. Phys., 20, 11955–11977, https://doi.org/10.5194/acp-20-11955-2020, https://doi.org/10.5194/acp-20-11955-2020, 2020
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Projected changes in man-made aerosol range from large reductions to moderate increases in emissions until 2050. Rapid reductions between the present and the 2050s lead to enhanced increases in global and Asian summer monsoon precipitation relative to scenarios with continued increases in aerosol. Relative magnitude and spatial distribution of aerosol changes are particularly important for South Asian summer monsoon precipitation changes, affecting the sign of the trend in the coming decades.
Luisa Ickes, Grace C. E. Porter, Robert Wagner, Michael P. Adams, Sascha Bierbauer, Allan K. Bertram, Merete Bilde, Sigurd Christiansen, Annica M. L. Ekman, Elena Gorokhova, Kristina Höhler, Alexei A. Kiselev, Caroline Leck, Ottmar Möhler, Benjamin J. Murray, Thea Schiebel, Romy Ullrich, and Matthew E. Salter
Atmos. Chem. Phys., 20, 11089–11117, https://doi.org/10.5194/acp-20-11089-2020, https://doi.org/10.5194/acp-20-11089-2020, 2020
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The Arctic is a region where aerosols are scarce. Sea spray might be a potential source of aerosols acting as ice-nucleating particles. We investigate two common phytoplankton species (Melosira arctica and Skeletonema marinoi) and present their ice nucleation activity in comparison with Arctic seawater microlayer samples from different field campaigns. We also aim to understand the aerosolization process of marine biological samples and the potential effect on the ice nucleation activity.
W. Richard Leaitch, John K. Kodros, Megan D. Willis, Sarah Hanna, Hannes Schulz, Elisabeth Andrews, Heiko Bozem, Julia Burkart, Peter Hoor, Felicia Kolonjari, John A. Ogren, Sangeeta Sharma, Meng Si, Knut von Salzen, Allan K. Bertram, Andreas Herber, Jonathan P. D. Abbatt, and Jeffrey R. Pierce
Atmos. Chem. Phys., 20, 10545–10563, https://doi.org/10.5194/acp-20-10545-2020, https://doi.org/10.5194/acp-20-10545-2020, 2020
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Black carbon is a factor in the warming of the Arctic atmosphere due to its ability to absorb light, but the uncertainty is high and few observations have been made in the high Arctic above 80° N. We combine airborne and ground-based observations in the springtime Arctic, at and above 80° N, with simulations from a global model to show that light absorption by black carbon may be much larger than modelled. However, the uncertainty remains high.
Anna Possner, Ryan Eastman, Frida Bender, and Franziska Glassmeier
Atmos. Chem. Phys., 20, 3609–3621, https://doi.org/10.5194/acp-20-3609-2020, https://doi.org/10.5194/acp-20-3609-2020, 2020
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Cloud water content and the number of droplets inside clouds covary with boundary layer depth. This covariation may amplify the change in water content due to a change in droplet number inferred from long-term observations. Taking this into account shows that the change in water content for increased droplet number in observations and high-resolution simulations agrees in shallow boundary layers. Meanwhile, deep boundary layers are under-sampled in process-scale simulations and observations.
Maria Sand, Terje K. Berntsen, Annica M. L. Ekman, Hans-Christen Hansson, and Anna Lewinschal
Atmos. Chem. Phys., 20, 3079–3089, https://doi.org/10.5194/acp-20-3079-2020, https://doi.org/10.5194/acp-20-3079-2020, 2020
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There has been a growing interest in reducing emissions of soot particles to slow global warming and improve air quality. However, estimating the effect of reduced emissions is complex, as soot particles absorb solar radiation and influence heating rates, clouds, and humidity and can influence climate far outside their emission region. Here we investigate the impact of soot emitted in four major emissions areas, using different emissions rates, to see whether location and magnitude matter.
Md. Robiul Islam, Thilina Jayarathne, Isobel J. Simpson, Benjamin Werden, John Maben, Ashley Gilbert, Puppala S. Praveen, Sagar Adhikari, Arnico K. Panday, Maheswar Rupakheti, Donald R. Blake, Robert J. Yokelson, Peter F. DeCarlo, William C. Keene, and Elizabeth A. Stone
Atmos. Chem. Phys., 20, 2927–2951, https://doi.org/10.5194/acp-20-2927-2020, https://doi.org/10.5194/acp-20-2927-2020, 2020
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The Kathmandu Valley experiences high levels of air pollution. In this study, atmospheric gases and particulate matter were characterized by online and off-line measurements, with an emphasis on understanding their sources. The major sources of particulate matter and trace gases were identified as garbage burning, biomass burning, and vehicles. The majority of secondary organic aerosol was attributed to anthropogenic precursors, while a minority was attributed to biogenic gases.
Georgia Sotiropoulou, Sylvia Sullivan, Julien Savre, Gary Lloyd, Thomas Lachlan-Cope, Annica M. L. Ekman, and Athanasios Nenes
Atmos. Chem. Phys., 20, 1301–1316, https://doi.org/10.5194/acp-20-1301-2020, https://doi.org/10.5194/acp-20-1301-2020, 2020
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Arctic clouds constitute a large source of uncertainty in predictions of future climate. Observations indicate that the number concentration of cloud ice crystals exceeds the concentration of aerosols that can act as ice-nucleating particles (INPs). We show that ice multiplication due to mechanical break-up upon collisions between the few primary ice crystals (formed from INPs) can explain the discrepancy. Including a description of the process in climate models can improve cloud representation.
Laura J. Wilcox, Nick Dunstone, Anna Lewinschal, Massimo Bollasina, Annica M. L. Ekman, and Eleanor J. Highwood
Atmos. Chem. Phys., 19, 9081–9095, https://doi.org/10.5194/acp-19-9081-2019, https://doi.org/10.5194/acp-19-9081-2019, 2019
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Asian anthropogenic aerosol emissions have increased rapidly since 1980. In winter, this has resulted in warming over China and cooling over India. Using models of different levels of complexity, we show that Asian-aerosol-induced heating anomalies in the western and northern North Pacific establish a circulation pattern that causes cooling in North America and Europe. This connection makes these regions potentially sensitive to any reductions of Asian aerosol emissions in the near future.
Anna Lewinschal, Annica M. L. Ekman, Hans-Christen Hansson, Maria Sand, Terje K. Berntsen, and Joakim Langner
Atmos. Chem. Phys., 19, 2385–2403, https://doi.org/10.5194/acp-19-2385-2019, https://doi.org/10.5194/acp-19-2385-2019, 2019
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We use a global climate model to study how anthropogenic emissions of short-lived atmospheric particles in different parts of the world influence the global temperature distribution. We find that the global mean temperature change per unit emission is similar for all emission regions, and the largest temperature response is found in the Arctic no matter where the emissions occur. However, for European emissions, the temperature change per unit emission is found to depend on emission strength.
Michael Boy, Erik S. Thomson, Juan-C. Acosta Navarro, Olafur Arnalds, Ekaterina Batchvarova, Jaana Bäck, Frank Berninger, Merete Bilde, Zoé Brasseur, Pavla Dagsson-Waldhauserova, Dimitri Castarède, Maryam Dalirian, Gerrit de Leeuw, Monika Dragosics, Ella-Maria Duplissy, Jonathan Duplissy, Annica M. L. Ekman, Keyan Fang, Jean-Charles Gallet, Marianne Glasius, Sven-Erik Gryning, Henrik Grythe, Hans-Christen Hansson, Margareta Hansson, Elisabeth Isaksson, Trond Iversen, Ingibjorg Jonsdottir, Ville Kasurinen, Alf Kirkevåg, Atte Korhola, Radovan Krejci, Jon Egill Kristjansson, Hanna K. Lappalainen, Antti Lauri, Matti Leppäranta, Heikki Lihavainen, Risto Makkonen, Andreas Massling, Outi Meinander, E. Douglas Nilsson, Haraldur Olafsson, Jan B. C. Pettersson, Nønne L. Prisle, Ilona Riipinen, Pontus Roldin, Meri Ruppel, Matthew Salter, Maria Sand, Øyvind Seland, Heikki Seppä, Henrik Skov, Joana Soares, Andreas Stohl, Johan Ström, Jonas Svensson, Erik Swietlicki, Ksenia Tabakova, Throstur Thorsteinsson, Aki Virkkula, Gesa A. Weyhenmeyer, Yusheng Wu, Paul Zieger, and Markku Kulmala
Atmos. Chem. Phys., 19, 2015–2061, https://doi.org/10.5194/acp-19-2015-2019, https://doi.org/10.5194/acp-19-2015-2019, 2019
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The Nordic Centre of Excellence CRAICC (Cryosphere–Atmosphere Interactions in a Changing Arctic Climate), funded by NordForsk in the years 2011–2016, is the largest joint Nordic research and innovation initiative to date and aimed to strengthen research and innovation regarding climate change issues in the Nordic region. The paper presents an overview of the main scientific topics investigated and provides a state-of-the-art comprehensive summary of what has been achieved in CRAICC.
J. Douglas Goetz, Michael R. Giordano, Chelsea E. Stockwell, Ted J. Christian, Rashmi Maharjan, Sagar Adhikari, Prakash V. Bhave, Puppala S. Praveen, Arnico K. Panday, Thilina Jayarathne, Elizabeth A. Stone, Robert J. Yokelson, and Peter F. DeCarlo
Atmos. Chem. Phys., 18, 14653–14679, https://doi.org/10.5194/acp-18-14653-2018, https://doi.org/10.5194/acp-18-14653-2018, 2018
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Size distributions and emission factors of submicron aerosol were quantified using online techniques for a variety of common but under-sampled combustion sources in South Asia: wood and dung cooking fires, groundwater pumps, brick kilns, trash burning, and open burning of crop residues. Optical properties (brown carbon light absorption and the absorption Ångström exponent, AAE) of the emissions were also investigated. Contextual comparisons to the literature and other NAMaSTE results were made.
Xiaona Shang, Meehye Lee, Saehee Lim, Örjan Gustafsson, Gangwoong Lee, and Limseok Chang
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2018-721, https://doi.org/10.5194/acp-2018-721, 2018
Preprint withdrawn
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At Gosan Climate Observatory, the three main sources including anthropogenic pollution, soil dust, and agricultural fertilizer were distinguished for PM10, PM2.5, and PM1, which accounted for 71 % of the total variances for their mass and composition. The mass of mean + σ were comparable to the 90th percentile and the top 10 % implies the substantial impact of soil dust and haze pollution. In PM2.5, the contribution from non-combustion source such as soil dust should not be ignored.
Lauren Schmeisser, John Backman, John A. Ogren, Elisabeth Andrews, Eija Asmi, Sandra Starkweather, Taneil Uttal, Markus Fiebig, Sangeeta Sharma, Kostas Eleftheriadis, Stergios Vratolis, Michael Bergin, Peter Tunved, and Anne Jefferson
Atmos. Chem. Phys., 18, 11599–11622, https://doi.org/10.5194/acp-18-11599-2018, https://doi.org/10.5194/acp-18-11599-2018, 2018
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This paper presents pan-Arctic seasonality of in-situ-measured aerosol optical properties from six surface monitoring sites. The analysis provides insight into aerosol annual variability throughout the region – something that is not possible using only measurements from satellite or temporary aircraft campaigns. This paper shows that the large spatiotemporal variability in aerosol optical properties needs to be taken into account in order to properly represent Arctic climate.
Robin G. Stevens, Katharina Loewe, Christopher Dearden, Antonios Dimitrelos, Anna Possner, Gesa K. Eirund, Tomi Raatikainen, Adrian A. Hill, Benjamin J. Shipway, Jonathan Wilkinson, Sami Romakkaniemi, Juha Tonttila, Ari Laaksonen, Hannele Korhonen, Paul Connolly, Ulrike Lohmann, Corinna Hoose, Annica M. L. Ekman, Ken S. Carslaw, and Paul R. Field
Atmos. Chem. Phys., 18, 11041–11071, https://doi.org/10.5194/acp-18-11041-2018, https://doi.org/10.5194/acp-18-11041-2018, 2018
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We perform a model intercomparison of summertime high Arctic clouds. Observed concentrations of aerosol particles necessary for cloud formation fell to extremely low values, coincident with a transition from cloudy to nearly cloud-free conditions. Previous analyses have suggested that at these low concentrations, the radiative properties of the clouds are determined primarily by these particle concentrations. The model results strongly support this hypothesis.
Héctor Rivera, John A. Ogren, Elisabeth Andrews, and Olga L. Mayol-Bracero
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2018-791, https://doi.org/10.5194/acp-2018-791, 2018
Preprint withdrawn
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This paper is about the variations of the physicochemical and optical properties of natural aerosols in Puerto Rico. We compare/contrast the implications of the loads, sizes, scattering, and absorbing properties of marine, African dust, and volcanic aerosols in the radiative forcing efficiency. We discuss how we classified these aerosols by source and their relative contribution to the radiative forcing efficiency. We contrast the change in temperature due to African dust and volcanic aerosols.
Quentin Bourgeois, Annica M. L. Ekman, Jean-Baptiste Renard, Radovan Krejci, Abhay Devasthale, Frida A.-M. Bender, Ilona Riipinen, Gwenaël Berthet, and Jason L. Tackett
Atmos. Chem. Phys., 18, 7709–7720, https://doi.org/10.5194/acp-18-7709-2018, https://doi.org/10.5194/acp-18-7709-2018, 2018
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The altitude of aerosols is crucial as they can impact cloud formation and radiation. In this study, satellite observations have been used to characterize the global aerosol optical depth (AOD) in the boundary layer and the free troposphere. The free troposphere contributes 39 % to the global AOD during daytime. Overall, the results have implications for the description of budgets, sources, sinks and transport of aerosol particles as presently described in the atmospheric model.
Daniel T. McCoy, Paul R. Field, Anja Schmidt, Daniel P. Grosvenor, Frida A.-M. Bender, Ben J. Shipway, Adrian A. Hill, Jonathan M. Wilkinson, and Gregory S. Elsaesser
Atmos. Chem. Phys., 18, 5821–5846, https://doi.org/10.5194/acp-18-5821-2018, https://doi.org/10.5194/acp-18-5821-2018, 2018
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Here we use a combination of global convection-permitting models, satellite observations and the Holuhraun volcanic eruption to demonstrate that aerosol enhances the cloud liquid content and brightness of midlatitude cyclones. This is important because the strength of anthropogenic radiative forcing is uncertain, leading to uncertainty in the climate sensitivity consistent with observed temperature record.
Chaman Gul, Siva Praveen Puppala, Shichang Kang, Bhupesh Adhikary, Yulan Zhang, Shaukat Ali, Yang Li, and Xiaofei Li
Atmos. Chem. Phys., 18, 4981–5000, https://doi.org/10.5194/acp-18-4981-2018, https://doi.org/10.5194/acp-18-4981-2018, 2018
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Snow and ice samples were collected from six glaciers and multiple mountain valleys from northern Pakistan. Samples were analyzed for black carbon and water-insoluble organic carbon. Relatively high concentrations of black carbon, organic carbon, and dust were reported. Snow albedo and radiative forcing were estimated for the snow samples. Possible source regions of pollutants were identified through various techniques.
Julia Schmale, Silvia Henning, Stefano Decesari, Bas Henzing, Helmi Keskinen, Karine Sellegri, Jurgita Ovadnevaite, Mira L. Pöhlker, Joel Brito, Aikaterini Bougiatioti, Adam Kristensson, Nikos Kalivitis, Iasonas Stavroulas, Samara Carbone, Anne Jefferson, Minsu Park, Patrick Schlag, Yoko Iwamoto, Pasi Aalto, Mikko Äijälä, Nicolas Bukowiecki, Mikael Ehn, Göran Frank, Roman Fröhlich, Arnoud Frumau, Erik Herrmann, Hartmut Herrmann, Rupert Holzinger, Gerard Kos, Markku Kulmala, Nikolaos Mihalopoulos, Athanasios Nenes, Colin O'Dowd, Tuukka Petäjä, David Picard, Christopher Pöhlker, Ulrich Pöschl, Laurent Poulain, André Stephan Henry Prévôt, Erik Swietlicki, Meinrat O. Andreae, Paulo Artaxo, Alfred Wiedensohler, John Ogren, Atsushi Matsuki, Seong Soo Yum, Frank Stratmann, Urs Baltensperger, and Martin Gysel
Atmos. Chem. Phys., 18, 2853–2881, https://doi.org/10.5194/acp-18-2853-2018, https://doi.org/10.5194/acp-18-2853-2018, 2018
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Collocated long-term observations of cloud condensation nuclei (CCN) number concentrations, particle number size distributions and chemical composition from 12 sites are synthesized. Observations cover coastal environments, the Arctic, the Mediterranean, the boreal and rain forest, high alpine and continental background sites, and Monsoon-influenced areas. We interpret regional and seasonal variability. CCN concentrations are predicted with the κ–Köhler model and compared to the measurements.
Thilina Jayarathne, Chelsea E. Stockwell, Prakash V. Bhave, Puppala S. Praveen, Chathurika M. Rathnayake, Md. Robiul Islam, Arnico K. Panday, Sagar Adhikari, Rashmi Maharjan, J. Douglas Goetz, Peter F. DeCarlo, Eri Saikawa, Robert J. Yokelson, and Elizabeth A. Stone
Atmos. Chem. Phys., 18, 2259–2286, https://doi.org/10.5194/acp-18-2259-2018, https://doi.org/10.5194/acp-18-2259-2018, 2018
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Emissions of fine particulate matter and its constituents were quantified for a variety of under-sampled combustion sources in South Asia: wood and dung cooking fires, generators, groundwater pumps, brick kilns, trash burning, and open burning of biomasses. Garbage burning and three-stone cooking fires were among the highest emitters, while servicing of motor vehicles significantly reduced PM. These data may be used in source apportionment and to update regional and global emission inventories.
Daniel T. McCoy, Frida A.-M. Bender, Daniel P. Grosvenor, Johannes K. Mohrmann, Dennis L. Hartmann, Robert Wood, and Paul R. Field
Atmos. Chem. Phys., 18, 2035–2047, https://doi.org/10.5194/acp-18-2035-2018, https://doi.org/10.5194/acp-18-2035-2018, 2018
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The interaction between clouds and aerosols represents the largest source of uncertainty in the anthropogenic radiative forcing. Cloud droplet number concentration (CDNC) is the state variable that moderates the interaction between aerosol and clouds. Here we show that CDNC decreases off the coasts of East Asia and North America due to controls on emissions. We support this analysis through an examination of volcanism in Hawaii and Vanuatu.
Sangeeta Sharma, W. Richard Leaitch, Lin Huang, Daniel Veber, Felicia Kolonjari, Wendy Zhang, Sarah J. Hanna, Allan K. Bertram, and John A. Ogren
Atmos. Chem. Phys., 17, 15225–15243, https://doi.org/10.5194/acp-17-15225-2017, https://doi.org/10.5194/acp-17-15225-2017, 2017
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A new and unique data set on BC properties at the highest latitude observatory in the world, at Alert, Canada, evaluates three techniques for estimating black carbon (BC) and gives seasonal best estimates of the BC mass concentrations and BC mass absorption coefficients (MAC) for 2.5 years of data. As a short-lived climate forcer, better estimates of the properties of BC are necessary to ensure accurate modelling of aerosol climate forcing of the Arctic atmosphere for mitigation purposes.
John Backman, Lauren Schmeisser, Aki Virkkula, John A. Ogren, Eija Asmi, Sandra Starkweather, Sangeeta Sharma, Konstantinos Eleftheriadis, Taneil Uttal, Anne Jefferson, Michael Bergin, Alexander Makshtas, Peter Tunved, and Markus Fiebig
Atmos. Meas. Tech., 10, 5039–5062, https://doi.org/10.5194/amt-10-5039-2017, https://doi.org/10.5194/amt-10-5039-2017, 2017
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Light absorption by aerosol particles is of climatic importance. A widely used means to measure aerosol light absorption is a filter-based measurement technique. In remote areas, such as the Arctic, filter-based instruments operate close to their detection limit. The study presents how a lower detection limit can be achieved for one such instrument, the Aethalometer. Additionally, the Aethalometer is compared to similar instruments, thus improving measurement inter-comparability in the Arctic.
John A. Ogren, Jim Wendell, Elisabeth Andrews, and Patrick J. Sheridan
Atmos. Meas. Tech., 10, 4805–4818, https://doi.org/10.5194/amt-10-4805-2017, https://doi.org/10.5194/amt-10-4805-2017, 2017
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A new photometer for continuous measurements of aerosol light absorption coefficient is described, optimized for long-term studies of the climate-forcing properties of aerosols. The device is small, sensitive, precise, and simple to operate. It is suitable for long-term measurements at remote locations and is currently in operation at about two dozen sites worldwide.
Chaeyoon Cho, Sang-Woo Kim, Maheswar Rupakheti, Jin-Soo Park, Arnico Panday, Soon-Chang Yoon, Ji-Hyoung Kim, Hyunjae Kim, Haeun Jeon, Minyoung Sung, Bong Mann Kim, Seungkyu K. Hong, Rokjin J. Park, Dipesh Rupakheti, Khadak Singh Mahata, Puppala Siva Praveen, Mark G. Lawrence, and Brent Holben
Atmos. Chem. Phys., 17, 12617–12632, https://doi.org/10.5194/acp-17-12617-2017, https://doi.org/10.5194/acp-17-12617-2017, 2017
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We investigated the optical and chemical properties and direct radiative effects of aerosols in the Kathmandu Valley. We concluded that the ratio of light-absorbing to scattering aerosols as well as the concentration of light-absorbing aerosols is much higher at Kathmandu than other comparable regions, and it contributes to a great atmospheric absorption efficiency. This study provides unprecedented insights into aerosol optical properties and their radiative forcings in the Kathmandu Valley.
Lauren Schmeisser, Elisabeth Andrews, John A. Ogren, Patrick Sheridan, Anne Jefferson, Sangeeta Sharma, Jeong Eun Kim, James P. Sherman, Mar Sorribas, Ivo Kalapov, Todor Arsov, Christo Angelov, Olga L. Mayol-Bracero, Casper Labuschagne, Sang-Woo Kim, András Hoffer, Neng-Huei Lin, Hao-Ping Chia, Michael Bergin, Junying Sun, Peng Liu, and Hao Wu
Atmos. Chem. Phys., 17, 12097–12120, https://doi.org/10.5194/acp-17-12097-2017, https://doi.org/10.5194/acp-17-12097-2017, 2017
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Three methods are used to classify aerosol type from aerosol optical properties measured in situ at 24 surface sites. Classification methods work best at sites with stable, homogenous aerosol at particularly polluted and dust-prone continental and marine sites. Classification methods are poor at remote marine and Arctic sites. Using these methods to extrapolate aerosol type from optical properties can help determine aerosol radiative forcing and improve aerosol satellite retrieval algorithms.
Dipesh Rupakheti, Bhupesh Adhikary, Puppala Siva Praveen, Maheswar Rupakheti, Shichang Kang, Khadak Singh Mahata, Manish Naja, Qianggong Zhang, Arnico Kumar Panday, and Mark G. Lawrence
Atmos. Chem. Phys., 17, 11041–11063, https://doi.org/10.5194/acp-17-11041-2017, https://doi.org/10.5194/acp-17-11041-2017, 2017
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For the first time, atmospheric composition was monitored during pre-monsoon season of 2013 at Lumbini (UNESCO world heritage site as birthplace of the Buddha). PM and O3 frequently exceeded WHO guidelines. Pollution concentration, diurnal characteristics and influence of open burning on air quality in Lumbini were investigated. Potential source regions were also identified. Results show that air pollution at this site is of a great concern, requiring prompt attention for mitigation.
Héctor Rivera, John A. Ogren, Elisabeth Andrews, and Olga L. Mayol-Bracero
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2017-703, https://doi.org/10.5194/acp-2017-703, 2017
Preprint withdrawn
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To lower the climate uncertainty by aerosols, we evaluated the radiative-forcing properties of aerosols in Puerto Rico analyzing their means and variability vs. amount, sizes, and light absorbing properties. Mean amounts, sizes, and absorbing properties differed among aerosol classes in the marine boundary layer and atmospheric column. Coarse African dust produced 50 % more cooling at the top of the atmosphere and temperature changes 50 % greater than volcanic ash within the marine boundary layer.
Lena Frey, Frida A.-M. Bender, and Gunilla Svensson
Atmos. Chem. Phys., 17, 9145–9162, https://doi.org/10.5194/acp-17-9145-2017, https://doi.org/10.5194/acp-17-9145-2017, 2017
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In this study, the cloud albedo effect in climate models is investigated, separating the influence of anthropogenic sulfate and non-sulfate aerosols. Cloud albedo changes induced by added anthropogenic aerosols are found to be determined by changes in the cloud water content rather than model sensitivity to monthly aerosol variations. The results also indicate that the background aerosol is the main driver for a cloud brightening effect on the month-to-month scale.
Katharina Loewe, Annica M. L. Ekman, Marco Paukert, Joseph Sedlar, Michael Tjernström, and Corinna Hoose
Atmos. Chem. Phys., 17, 6693–6704, https://doi.org/10.5194/acp-17-6693-2017, https://doi.org/10.5194/acp-17-6693-2017, 2017
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Processes that affect Arctic mixed-phase cloud life cycle are extremely important for the surface energy budget. Three different sensitivity experiments mimic changes in the advection of air masses with different thermodynamic profiles and aerosol properties to find the potential mechanisms leading to the dissipation of the cloud. We found that the reduction of the cloud droplet number concentration was likely the primary contributor to the dissipation of the observed Arctic mixed-phase cloud.
Kabindra M. Shakya, Maheswar Rupakheti, Anima Shahi, Rejina Maskey, Bidya Pradhan, Arnico Panday, Siva P. Puppala, Mark Lawrence, and Richard E. Peltier
Atmos. Chem. Phys., 17, 6503–6516, https://doi.org/10.5194/acp-17-6503-2017, https://doi.org/10.5194/acp-17-6503-2017, 2017
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Particulate matter levels were monitored at six major roadway intersections in the Kathmandu Valley during two seasons in 2014. The study documented distinct seasonal (dry season versus wet season) and diel variations in particulate matter levels. This study suggests traffic-related emissions, and soil–dust–construction materials were found to be a major source of particulate matter at these locations.
Elisabeth Andrews, John A. Ogren, Stefan Kinne, and Bjorn Samset
Atmos. Chem. Phys., 17, 6041–6072, https://doi.org/10.5194/acp-17-6041-2017, https://doi.org/10.5194/acp-17-6041-2017, 2017
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We compare absorption aerosol optical depth (AAOD) and single scattering albedo (SSA) from AERONET retrievals with AAOD and SSA obtained from in situ vertical profiling flights over two rural sites in North America. The direct comparisons of in situ derived to AERONET-retrieved AAOD (or SSA) reveal that AERONET retrievals yield higher aerosol absorption than obtained from the in situ profiles. This has implications for models using AERONET to evaluate or scale their simulated absorption values.
Sujan Shrestha, Siva Praveen Puppala, Bhupesh Adhikary, Kundan Lal Shrestha, and Arnico K. Panday
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2017-287, https://doi.org/10.5194/acp-2017-287, 2017
Revised manuscript not accepted
Chelsea E. Stockwell, Ted J. Christian, J. Douglas Goetz, Thilina Jayarathne, Prakash V. Bhave, Puppala S. Praveen, Sagar Adhikari, Rashmi Maharjan, Peter F. DeCarlo, Elizabeth A. Stone, Eri Saikawa, Donald R. Blake, Isobel J. Simpson, Robert J. Yokelson, and Arnico K. Panday
Atmos. Chem. Phys., 16, 11043–11081, https://doi.org/10.5194/acp-16-11043-2016, https://doi.org/10.5194/acp-16-11043-2016, 2016
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We present the first, or rare, field measurements in South Asia of emission factors for up to 80 gases (pollutants, greenhouse gases, and precursors) and black carbon and aerosol optical properties at 405 and 870 nm for many previously under-sampled sources that are important in developing countries such as cooking with dung and wood, garbage and crop residue burning, brick kilns, motorcycles, generators and pumps, etc. Brown carbon contributes significantly to total aerosol absorption.
Kristina Pistone, Puppala S. Praveen, Rick M. Thomas, Veerabhadran Ramanathan, Eric M. Wilcox, and Frida A.-M. Bender
Atmos. Chem. Phys., 16, 5203–5227, https://doi.org/10.5194/acp-16-5203-2016, https://doi.org/10.5194/acp-16-5203-2016, 2016
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A recent field campaign (CARDEX) in the northern Indian Ocean concurrently measured cloud and aerosol properties and atmospheric structure and dynamics from a ground-based observatory and unmanned aerial vehicles (UAVs). These new measurements show a correlation between highly polluted conditions and increased cloud water content, concurrent with higher atmospheric temperature and humidity. Such correlations may be of interest in future studies of the effects of pollution on cloud properties.
Y. Xu, V. Ramanathan, and W. M. Washington
Atmos. Chem. Phys., 16, 1303–1315, https://doi.org/10.5194/acp-16-1303-2016, https://doi.org/10.5194/acp-16-1303-2016, 2016
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We show that black carbon aerosol pollution is likely the dominant factor in causing the accelerated retreat of snowpack in Himalayas. The simulated snow fraction and surface albedo change at the surface, as well as the enhanced warming at higher elevations, are remarkably similar to observations in past decades. The reason for the model's ability to simulate the observed trends is that we replace the model-simulated black carbon forcing with one that is constrained by observations.
E. W. Butt, A. Rap, A. Schmidt, C. E. Scott, K. J. Pringle, C. L. Reddington, N. A. D. Richards, M. T. Woodhouse, J. Ramirez-Villegas, H. Yang, V. Vakkari, E. A. Stone, M. Rupakheti, P. S. Praveen, P. G. van Zyl, J. P. Beukes, M. Josipovic, E. J. S. Mitchell, S. M. Sallu, P. M. Forster, and D. V. Spracklen
Atmos. Chem. Phys., 16, 873–905, https://doi.org/10.5194/acp-16-873-2016, https://doi.org/10.5194/acp-16-873-2016, 2016
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We estimate the impact of residential emissions (cooking and heating) on atmospheric aerosol, human health, and climate. We find large contributions to annual mean ambient PM2.5 in residential sources regions resulting in significant but uncertain global premature mortality when key uncertainties in emission flux are considered. We show that residential emissions exert an uncertain global radiative effect and suggest more work is needed to characterise residential emissions climate importance.
A. G. Hallar, R. Petersen, E. Andrews, J. Michalsky, I. B. McCubbin, and J. A. Ogren
Atmos. Chem. Phys., 15, 13665–13679, https://doi.org/10.5194/acp-15-13665-2015, https://doi.org/10.5194/acp-15-13665-2015, 2015
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The atmospheric seasonal impact of dust and biomass burning is considered for the western United States from 1999 to 2014. Median contributions to spring and summer aerosol optical depth (AOD) from dust and biomass-burning aerosols are comparable, with more frequent and short duration high AOD measurements due to biomass-burning episodes in summer than in spring. This data set highlights the wide scale implications of a warmer, drier climate on visibility in the western US.
J. P. Sherman, P. J. Sheridan, J. A. Ogren, E. Andrews, D. Hageman, L. Schmeisser, A. Jefferson, and S. Sharma
Atmos. Chem. Phys., 15, 12487–12517, https://doi.org/10.5194/acp-15-12487-2015, https://doi.org/10.5194/acp-15-12487-2015, 2015
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Variability in aerosol optical properties relevant to radiative forcing were studied on several timescales at four continental North American NOAA-ESRL sites. Light scattering and intensive properties varied most on seasonal scales while absorption variability on weekly and diurnal timescales was comparable to its seasonal variability. Large reductions in light scattering were observed at the two long-term sites (relative to late 1990s), along with a smaller contribution by sub-1µm particles.
E. Johansson, A. Devasthale, T. L'Ecuyer, A. M. L. Ekman, and M. Tjernström
Atmos. Chem. Phys., 15, 11557–11570, https://doi.org/10.5194/acp-15-11557-2015, https://doi.org/10.5194/acp-15-11557-2015, 2015
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Both radiative and latent heat components of total diabatic heating influence Indian monsoon dynamics. This study investigates radiative component in detail, focusing on various cloud types that have largest radiative impact during summer monsoon over the Indian subcontinent. The vertical structure of radiative heating and its intra-seasonal variability is investigated with particular emphasis on the upper troposphere and lower stratosphere (UTLS) region.
X. Feng, Ö. Gustafsson, R. M. Holmes, J. E. Vonk, B. E. van Dongen, I. P. Semiletov, O. V. Dudarev, M. B. Yunker, R. W. Macdonald, D. B. Montluçon, and T. I. Eglinton
Biogeosciences, 12, 4841–4860, https://doi.org/10.5194/bg-12-4841-2015, https://doi.org/10.5194/bg-12-4841-2015, 2015
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Currently very few studies have examined the distribution and fate of hydrolyzable organic carbon (OC) in Arctic sediments, whose fate remains unclear in the context of climate change. Our study focuses on the source, distribution and fate of hydrolyzable OC as compared with plant wax lipids and lignin phenols in the sedimentary particles of nine Arctic and sub-Arctic rivers. This multi-molecular approach allows for a comprehensive investigation of terrestrial OC transfer via Arctic rivers.
L. Zhang, J. Y. Sun, X. J. Shen, Y. M. Zhang, H. Che, Q. L. Ma, Y. W. Zhang, X. Y. Zhang, and J. A. Ogren
Atmos. Chem. Phys., 15, 8439–8454, https://doi.org/10.5194/acp-15-8439-2015, https://doi.org/10.5194/acp-15-8439-2015, 2015
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The aerosol hygroscopic properties at a rural background site in the Yangtze River delta of China was discussed. The results show the scattering coefficient and backscattering coefficient increased by 58 and 25% as relative humidity (RH) increased from 40 to 85%, while the hemispheric backscatter fraction decreased by 21%. Aerosol hygroscopic growth caused a 47% increase in calculated aerosol direct radiative forcing at 85% RH compared to the forcing at 40% RH. Nitrate played a vital role.
T. Müller, A. Virkkula, and J. A. Ogren
Atmos. Meas. Tech., 7, 4049–4070, https://doi.org/10.5194/amt-7-4049-2014, https://doi.org/10.5194/amt-7-4049-2014, 2014
N. Rastak, S. Silvergren, P. Zieger, U. Wideqvist, J. Ström, B. Svenningsson, M. Maturilli, M. Tesche, A. M. L. Ekman, P. Tunved, and I. Riipinen
Atmos. Chem. Phys., 14, 7445–7460, https://doi.org/10.5194/acp-14-7445-2014, https://doi.org/10.5194/acp-14-7445-2014, 2014
G. Titos, A. Jefferson, P. J. Sheridan, E. Andrews, H. Lyamani, L. Alados-Arboledas, and J. A. Ogren
Atmos. Chem. Phys., 14, 7031–7043, https://doi.org/10.5194/acp-14-7031-2014, https://doi.org/10.5194/acp-14-7031-2014, 2014
G. W. Mann, K. S. Carslaw, C. L. Reddington, K. J. Pringle, M. Schulz, A. Asmi, D. V. Spracklen, D. A. Ridley, M. T. Woodhouse, L. A. Lee, K. Zhang, S. J. Ghan, R. C. Easter, X. Liu, P. Stier, Y. H. Lee, P. J. Adams, H. Tost, J. Lelieveld, S. E. Bauer, K. Tsigaridis, T. P. C. van Noije, A. Strunk, E. Vignati, N. Bellouin, M. Dalvi, C. E. Johnson, T. Bergman, H. Kokkola, K. von Salzen, F. Yu, G. Luo, A. Petzold, J. Heintzenberg, A. Clarke, J. A. Ogren, J. Gras, U. Baltensperger, U. Kaminski, S. G. Jennings, C. D. O'Dowd, R. M. Harrison, D. C. S. Beddows, M. Kulmala, Y. Viisanen, V. Ulevicius, N. Mihalopoulos, V. Zdimal, M. Fiebig, H.-C. Hansson, E. Swietlicki, and J. S. Henzing
Atmos. Chem. Phys., 14, 4679–4713, https://doi.org/10.5194/acp-14-4679-2014, https://doi.org/10.5194/acp-14-4679-2014, 2014
M. Fiebig, D. Hirdman, C. R. Lunder, J. A. Ogren, S. Solberg, A. Stohl, and R. L. Thompson
Atmos. Chem. Phys., 14, 3083–3093, https://doi.org/10.5194/acp-14-3083-2014, https://doi.org/10.5194/acp-14-3083-2014, 2014
C. Wesslén, M. Tjernström, D. H. Bromwich, G. de Boer, A. M. L. Ekman, L.-S. Bai, and S.-H. Wang
Atmos. Chem. Phys., 14, 2605–2624, https://doi.org/10.5194/acp-14-2605-2014, https://doi.org/10.5194/acp-14-2605-2014, 2014
A. Cazorla, R. Bahadur, K. J. Suski, J. F. Cahill, D. Chand, B. Schmid, V. Ramanathan, and K. A. Prather
Atmos. Chem. Phys., 13, 9337–9350, https://doi.org/10.5194/acp-13-9337-2013, https://doi.org/10.5194/acp-13-9337-2013, 2013
Y. Feng, V. Ramanathan, and V. R. Kotamarthi
Atmos. Chem. Phys., 13, 8607–8621, https://doi.org/10.5194/acp-13-8607-2013, https://doi.org/10.5194/acp-13-8607-2013, 2013
A. Petzold, J. A. Ogren, M. Fiebig, P. Laj, S.-M. Li, U. Baltensperger, T. Holzer-Popp, S. Kinne, G. Pappalardo, N. Sugimoto, C. Wehrli, A. Wiedensohler, and X.-Y. Zhang
Atmos. Chem. Phys., 13, 8365–8379, https://doi.org/10.5194/acp-13-8365-2013, https://doi.org/10.5194/acp-13-8365-2013, 2013
Y. Xu, D. Zaelke, G. J. M. Velders, and V. Ramanathan
Atmos. Chem. Phys., 13, 6083–6089, https://doi.org/10.5194/acp-13-6083-2013, https://doi.org/10.5194/acp-13-6083-2013, 2013
J. Zábori, R. Krejci, J. Ström, P. Vaattovaara, A. M. L. Ekman, M. E. Salter, E. M. Mårtensson, and E. D. Nilsson
Atmos. Chem. Phys., 13, 4783–4799, https://doi.org/10.5194/acp-13-4783-2013, https://doi.org/10.5194/acp-13-4783-2013, 2013
A. Kirkevåg, T. Iversen, Ø. Seland, C. Hoose, J. E. Kristjánsson, H. Struthers, A. M. L. Ekman, S. Ghan, J. Griesfeller, E. D. Nilsson, and M. Schulz
Geosci. Model Dev., 6, 207–244, https://doi.org/10.5194/gmd-6-207-2013, https://doi.org/10.5194/gmd-6-207-2013, 2013
A. Asmi, M. Collaud Coen, J. A. Ogren, E. Andrews, P. Sheridan, A. Jefferson, E. Weingartner, U. Baltensperger, N. Bukowiecki, H. Lihavainen, N. Kivekäs, E. Asmi, P. P. Aalto, M. Kulmala, A. Wiedensohler, W. Birmili, A. Hamed, C. O'Dowd, S. G Jennings, R. Weller, H. Flentje, A. M. Fjaeraa, M. Fiebig, C. L. Myhre, A. G. Hallar, E. Swietlicki, A. Kristensson, and P. Laj
Atmos. Chem. Phys., 13, 895–916, https://doi.org/10.5194/acp-13-895-2013, https://doi.org/10.5194/acp-13-895-2013, 2013
M. Collaud Coen, E. Andrews, A. Asmi, U. Baltensperger, N. Bukowiecki, D. Day, M. Fiebig, A. M. Fjaeraa, H. Flentje, A. Hyvärinen, A. Jefferson, S. G. Jennings, G. Kouvarakis, H. Lihavainen, C. Lund Myhre, W. C. Malm, N. Mihapopoulos, J. V. Molenar, C. O'Dowd, J. A. Ogren, B. A. Schichtel, P. Sheridan, A. Virkkula, E. Weingartner, R. Weller, and P. Laj
Atmos. Chem. Phys., 13, 869–894, https://doi.org/10.5194/acp-13-869-2013, https://doi.org/10.5194/acp-13-869-2013, 2013
P. J. Sheridan, E. Andrews, J. A. Ogren, J. L. Tackett, and D. M. Winker
Atmos. Chem. Phys., 12, 11695–11721, https://doi.org/10.5194/acp-12-11695-2012, https://doi.org/10.5194/acp-12-11695-2012, 2012
Related subject area
Subject: Aerosols | Research Activity: Field Measurements | Altitude Range: Troposphere | Science Focus: Physics (physical properties and processes)
Brownness of organics in anthropogenic biomass burning aerosols over South Asia
Source apportionment of particle number size distribution at the street canyon and urban background sites
Long-range transport of coarse mineral dust: an evaluation of the Met Office Unified Model against aircraft observations
Extreme Saharan dust events expand northward over the Atlantic and Europe, prompting record-breaking PM10 and PM2.5 episodes
Atmospheric black carbon in the metropolitan area of La Paz and El Alto, Bolivia: concentration levels and emission sources
Changing optical properties of black carbon and brown carbon aerosols during long-range transport from the Indo-Gangetic Plain to the equatorial Indian Ocean
Aerosol size distribution properties associated with cold-air outbreaks in the Norwegian Arctic
Ice-nucleating particles active below −24 °C in a Finnish boreal forest and their relationship to bioaerosols
Measurements of particle emissions of an A350-941 burning 100 % sustainable aviation fuels in cruise
Vertical distribution of ice nucleating particles over the boreal forest of Hyytiälä, Finland
Multi-year gradient measurements of sea spray fluxes over the Baltic Sea and the North Atlantic Ocean
External particle mixing influences hygroscopicity in a sub-urban area
Measurement report: In situ vertical profiles of below-cloud aerosol over the central Greenland Ice Sheet
Occurrence, abundance, and formation of atmospheric tarballs from a wide range of wildfires in the western US
Measurement report: Contribution of atmospheric new particle formation to ultrafine particle concentration, cloud condensation nuclei, and radiative forcing – results from 5-year observations in central Europe
Simulated contrail-processed aviation soot aerosols are poor ice-nucleating particles at cirrus temperatures
Biological and dust aerosols as sources of ice-nucleating particles in the eastern Mediterranean: source apportionment, atmospheric processing and parameterization
Quantifying the dust direct radiative effect in the southwestern United States: findings from multiyear measurements
How horizontal transport and turbulent mixing impact aerosol particle and precursor concentrations at a background site in the UAE
Markedly different impacts of primary emissions and secondary aerosol formation on aerosol mixing states revealed by simultaneous measurements of CCNC, H(/V)TDMA, and SP2
Vertically resolved aerosol variability at the Amazon Tall Tower Observatory under wet-season conditions
Measurement report: Analysis of aerosol optical depth variation at Zhongshan Station in Antarctica
Vertical structure of a springtime smoky and humid troposphere over the southeast Atlantic from aircraft and reanalysis
Quantification and characterization of primary biological aerosol particles and bacteria aerosolized from Baltic seawater
Shipborne observations of black carbon aerosols in the western Arctic Ocean during summer and autumn 2016–2020: impact of boreal fires
High ice-nucleating particle concentrations associated with Arctic haze in springtime cold-air outbreaks
CCN estimations at a high-altitude remote site: role of organic aerosol variability and hygroscopicity
Attribution of aerosol particle number size distributions to main sources using an 11-year urban dataset
Large Spatiotemporal Variability in Aerosol Properties over Central Argentina during the CACTI Field Campaign
Contribution of fluorescent primary biological aerosol particles to low-level Arctic cloud residuals
Opinion: New directions in atmospheric research offered by research infrastructures combined with open and data-intensive science
Measurement report: A comparison of ground-level ice-nucleating-particle abundance and aerosol properties during autumn at contrasting marine and terrestrial locations
Efficient droplet activation of ambient black carbon particles in a suburban environment
Tropospheric sulfate from Cumbre Vieja (La Palma) observed over Cabo Verde contrasted with background conditions: a lidar case study of aerosol extinction, backscatter, depolarization and lidar ratio profiles at 355, 532 and 1064 nm
The radiative impact of biomass burning aerosols on dust emissions over Namibia and the long-range transport of smoke observed during the Aerosols, Radiation and Clouds in southern Africa (AEROCLO-sA) campaign
Extending the wind profile beyond the surface layer by combining physical and machine learning approaches
Amazonian aerosol size distributions in a lognormal phase space: characteristics and trajectories
Measurement report: Hygroscopicity of size-selected aerosol particles in the heavily polluted urban atmosphere of Delhi: impacts of chloride aerosol
An observation-constrained estimation of brown carbon aerosol direct radiative effects
The Puy de Dôme ICe Nucleation Intercomparison Campaign (PICNIC): comparison between online and offline methods in ambient air
Optical properties and simple forcing efficiency of the organic aerosols and black carbon emitted by residential wood burning in rural central Europe
Particle phase state and aerosol liquid water greatly impact secondary aerosol formation: insights into phase transition and its role in haze events
Measurement Report: Comparative Analysis of Fluorescing African Dust Particles in Spain and Puerto Rico
Measurement report: Nocturnal subsidence behind the cold front enhances surface particulate matter in plains regions: observations from the mobile multi-lidar system
Increase in precipitation scavenging contributes to long-term reductions of light-absorbing aerosol in the Arctic
Sea spray emissions from the Baltic Sea: comparison of aerosol eddy covariance fluxes and chamber-simulated sea spray emissions
Higher absorption enhancement of black carbon in summer shown by 2-year measurements at the high-altitude mountain site of Pic du Midi Observatory in the French Pyrenees
Variations of the atmospheric polycyclic aromatic hydrocarbon concentrations, sources, and health risk and the direct medical costs of lung cancer around the Bohai Sea against a background of pollution prevention and control in China
The Spatial and Temporal Impact of the February 26, 2023, Dust Storm on the Meteorological Conditions and Particulate Matter Concentrations Across New Mexico and West Texas
Characterization of aerosol over the Eastern Mediterranean by polarization sensitive Raman lidar measurements during A-LIFE – aerosol type classification and type separation
Chimurkar Navinya, Taveen Singh Kapoor, Gupta Anurag, Chandra Venkataraman, Harish C. Phuleria, and Rajan K. Chakrabarty
Atmos. Chem. Phys., 24, 13285–13297, https://doi.org/10.5194/acp-24-13285-2024, https://doi.org/10.5194/acp-24-13285-2024, 2024
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Brown carbon (BrC) aerosols show an order-of-magnitude variation in their light absorption strength. Our understanding of BrC from real-world biomass burning remains limited, complicating the determination of its radiative impact. Our study reports absorption properties of BrC emitted from four major biomass burning sources using field measurements in India. It develops an absorption parameterization for BrC and examines the spatial variability in BrC's absorption strength across India.
Sami D. Harni, Minna Aurela, Sanna Saarikoski, Jarkko V. Niemi, Harri Portin, Hanna Manninen, Ville Leinonen, Pasi Aalto, Phil K. Hopke, Tuukka Petäjä, Topi Rönkkö, and Hilkka Timonen
Atmos. Chem. Phys., 24, 12143–12160, https://doi.org/10.5194/acp-24-12143-2024, https://doi.org/10.5194/acp-24-12143-2024, 2024
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In this study, particle number size distribution data were used in a novel way in positive matrix factorization analysis to find aerosol source profiles in the area. Measurements were made in Helsinki at a street canyon and urban background sites between February 2015 and June 2019. Five different aerosol sources were identified. These sources underline the significance of traffic-related emissions in urban environments despite recent improvements in emission reduction technologies.
Natalie G. Ratcliffe, Claire L. Ryder, Nicolas Bellouin, Stephanie Woodward, Anthony Jones, Ben Johnson, Lisa-Maria Wieland, Maximilian Dollner, Josef Gasteiger, and Bernadett Weinzierl
Atmos. Chem. Phys., 24, 12161–12181, https://doi.org/10.5194/acp-24-12161-2024, https://doi.org/10.5194/acp-24-12161-2024, 2024
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Large mineral dust particles are more abundant in the atmosphere than expected and have different impacts on the environment than small particles, which are better represented in climate models. We use aircraft measurements to assess a climate model representation of large-dust transport. We find that the model underestimates the amount of large dust at all stages of transport and that fast removal of the large particles increases this underestimation with distance from the Sahara.
Sergio Rodríguez and Jessica López-Darias
Atmos. Chem. Phys., 24, 12031–12053, https://doi.org/10.5194/acp-24-12031-2024, https://doi.org/10.5194/acp-24-12031-2024, 2024
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Extreme Saharan dust events expanded northward to the Atlantic and Europe, prompting record-breaking PM10 and PM2.5 events. These episodes are caused by low-to-high dipole meteorology during hemispheric anomalies characterized by subtropical anticyclones shifting to higher latitudes, anomalous low pressures beyond the tropics and amplified Rossby waves. Extreme dust events occur in a paradoxical context of a multidecadal decrease in dust emissions, a topic that requires further investigation.
Valeria Mardoñez-Balderrama, Griša Močnik, Marco Pandolfi, Robin L. Modini, Fernando Velarde, Laura Renzi, Angela Marinoni, Jean-Luc Jaffrezo, Isabel Moreno R., Diego Aliaga, Federico Bianchi, Claudia Mohr, Martin Gysel-Beer, Patrick Ginot, Radovan Krejci, Alfred Wiedensohler, Gaëlle Uzu, Marcos Andrade, and Paolo Laj
Atmos. Chem. Phys., 24, 12055–12077, https://doi.org/10.5194/acp-24-12055-2024, https://doi.org/10.5194/acp-24-12055-2024, 2024
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Levels of black carbon (BC) are scarcely reported in the Southern Hemisphere, especially in high-altitude conditions. This study provides insight into the concentration level, variability, and optical properties of BC in La Paz and El Alto and at the Chacaltaya Global Atmosphere Watch Station. Two methods of source apportionment of absorption were tested and compared showing traffic as the main contributor to absorption in the urban area, in addition to biomass and open waste burning.
Krishnakant Budhavant, Mohanan Remani Manoj, Hari Ram Chandrika Rajendran Nair, Samuel Mwaniki Gaita, Henry Holmstrand, Abdus Salam, Ahmed Muslim, Sreedharan Krishnakumari Satheesh, and Örjan Gustafsson
Atmos. Chem. Phys., 24, 11911–11925, https://doi.org/10.5194/acp-24-11911-2024, https://doi.org/10.5194/acp-24-11911-2024, 2024
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The South Asian Pollution Experiment 2018 used access to three strategically located receptor observatories. Observational constraints revealed opposing trends in the mass absorption cross sections of black carbon (BC MAC) and brown carbon (BrC MAC) during long-range transport. Models estimating the climate effects of BC aerosols may have underestimated the ambient BC MAC over distant receptor areas, leading to discrepancies in aerosol absorption predicted by observation-constrained models.
Abigail S. Williams, Jeramy L. Dedrick, Lynn M. Russell, Florian Tornow, Israel Silber, Ann M. Fridlind, Benjamin Swanson, Paul J. DeMott, Paul Zieger, and Radovan Krejci
Atmos. Chem. Phys., 24, 11791–11805, https://doi.org/10.5194/acp-24-11791-2024, https://doi.org/10.5194/acp-24-11791-2024, 2024
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The measured aerosol size distribution modes reveal distinct properties characteristic of cold-air outbreaks in the Norwegian Arctic. We find higher sea spray number concentrations, smaller Hoppel minima, lower effective supersaturations, and accumulation-mode particle scavenging during cold-air outbreaks. These results advance our understanding of cold-air outbreak aerosol–cloud interactions in order to improve their accurate representation in models.
Franziska Vogel, Michael P. Adams, Larissa Lacher, Polly B. Foster, Grace C. E. Porter, Barbara Bertozzi, Kristina Höhler, Julia Schneider, Tobias Schorr, Nsikanabasi S. Umo, Jens Nadolny, Zoé Brasseur, Paavo Heikkilä, Erik S. Thomson, Nicole Büttner, Martin I. Daily, Romy Fösig, Alexander D. Harrison, Jorma Keskinen, Ulrike Proske, Jonathan Duplissy, Markku Kulmala, Tuukka Petäjä, Ottmar Möhler, and Benjamin J. Murray
Atmos. Chem. Phys., 24, 11737–11757, https://doi.org/10.5194/acp-24-11737-2024, https://doi.org/10.5194/acp-24-11737-2024, 2024
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Primary ice formation in clouds strongly influences their properties; hence, it is important to understand the sources of ice-nucleating particles (INPs) and their variability. We present 2 months of INP measurements in a Finnish boreal forest using a new semi-autonomous INP counting device based on gas expansion. These results show strong variability in INP concentrations, and we present a case that the INPs we observe are, at least some of the time, of biological origin.
Rebecca Dischl, Daniel Sauer, Christiane Voigt, Theresa Harlaß, Felicitas Sakellariou, Raphael Märkl, Ulrich Schumann, Monika Scheibe, Stefan Kaufmann, Anke Roiger, Andreas Dörnbrack, Charles Renard, Maxime Gauthier, Peter Swann, Paul Madden, Darren Luff, Mark Johnson, Denise Ahrens, Reetu Sallinen, Tobias Schripp, Georg Eckel, Uwe Bauder, and Patrick Le Clercq
Atmos. Chem. Phys., 24, 11255–11273, https://doi.org/10.5194/acp-24-11255-2024, https://doi.org/10.5194/acp-24-11255-2024, 2024
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In-flight measurements of aircraft emissions burning 100 % sustainable aviation fuel (SAF) show reduced particle number concentrations up to 41 % compared to conventional jet fuel. Particle emissions are dependent on engine power setting, flight altitude, and fuel composition. Engine models show a good correlation with measurement results. Future increased prevalence of SAF can positively influence the climate impact of aviation.
Zoé Brasseur, Julia Schneider, Janne Lampilahti, Ville Vakkari, Victoria A. Sinclair, Christina J. Williamson, Carlton Xavier, Dmitri Moisseev, Markus Hartmann, Pyry Poutanen, Markus Lampimäki, Markku Kulmala, Tuukka Petäjä, Katrianne Lehtipalo, Erik S. Thomson, Kristina Höhler, Ottmar Möhler, and Jonathan Duplissy
Atmos. Chem. Phys., 24, 11305–11332, https://doi.org/10.5194/acp-24-11305-2024, https://doi.org/10.5194/acp-24-11305-2024, 2024
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Ice-nucleating particles (INPs) strongly influence the formation of clouds by initiating the formation of ice crystals. However, very little is known about the vertical distribution of INPs in the atmosphere. Here, we present aircraft measurements of INP concentrations above the Finnish boreal forest. Results show that near-surface INPs are efficiently transported and mixed within the boundary layer and occasionally reach the free troposphere.
Piotr Markuszewski, E. Douglas Nilsson, Julika Zinke, E. Monica Mårtensson, Matthew Salter, Przemysław Makuch, Małgorzata Kitowska, Iwona Niedźwiecka-Wróbel, Violetta Drozdowska, Dominik Lis, Tomasz Petelski, Luca Ferrero, and Jacek Piskozub
Atmos. Chem. Phys., 24, 11227–11253, https://doi.org/10.5194/acp-24-11227-2024, https://doi.org/10.5194/acp-24-11227-2024, 2024
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Our research provides new insights into the study of sea spray aerosol (SSA) emissions in the Baltic Sea and North Atlantic. We observed that SSA flux is suppressed during increased marine biological activity in the Baltic Sea. At the same time, the influence of wave age showed higher SSA emissions in the Baltic Sea for younger waves compared to the Atlantic Ocean. These insights underscore the complex interplay between biological activity and physical dynamics in regulating SSA emissions.
Shravan Deshmukh, Laurent Poulain, Birgit Wehner, Silvia Henning, Jean-Eudes Petit, Pauline Fombelle, Olivier Favez, Hartmut Herrmann, and Mira Pöhlker
EGUsphere, https://doi.org/10.5194/egusphere-2024-3027, https://doi.org/10.5194/egusphere-2024-3027, 2024
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Aerosol hygroscopicity has been investigated at the sub-urban site in Paris; analysis shows the sub-saturated regime's measured hygroscopicity and the chemically derived hygroscopic growth, shedding light on the large effect of external particle mixing and its influence on predicting hygroscopicity.
Heather Guy, Andrew S. Martin, Erik Olson, Ian M. Brooks, and Ryan R. Neely III
Atmos. Chem. Phys., 24, 11103–11114, https://doi.org/10.5194/acp-24-11103-2024, https://doi.org/10.5194/acp-24-11103-2024, 2024
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Aerosol particles impact cloud properties which influence Greenland Ice Sheet melt. Understanding the aerosol population that interacts with clouds is important for constraining future melt. Measurements of aerosols at cloud height over Greenland are rare, and surface measurements are often used to investigate cloud–aerosol interactions. We use a tethered balloon to measure aerosols up to cloud base and show that surface measurements are often not equivalent to those just below the cloud.
Kouji Adachi, Jack E. Dibb, Joseph M. Katich, Joshua P. Schwarz, Hongyu Guo, Pedro Campuzano-Jost, Jose L. Jimenez, Jeff Peischl, Christopher D. Holmes, and James Crawford
Atmos. Chem. Phys., 24, 10985–11004, https://doi.org/10.5194/acp-24-10985-2024, https://doi.org/10.5194/acp-24-10985-2024, 2024
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We examined aerosol particles from wildfires and identified tarballs (TBs) from the Fire Influence on Regional to Global Environments and Air Quality (FIREX-AQ) campaign. This study reveals the compositions, abundance, sizes, and mixing states of TBs and shows that TBs formed as the smoke aged for up to 5 h. This study provides measurements of TBs from various biomass-burning events and ages, enhancing our knowledge of TB emissions and our understanding of their climate impact.
Jia Sun, Markus Hermann, Kay Weinhold, Maik Merkel, Wolfram Birmili, Yifan Yang, Thomas Tuch, Harald Flentje, Björn Briel, Ludwig Ries, Cedric Couret, Michael Elsasser, Ralf Sohmer, Klaus Wirtz, Frank Meinhardt, Maik Schütze, Olaf Bath, Bryan Hellack, Veli-Matti Kerminen, Markku Kulmala, Nan Ma, and Alfred Wiedensohler
Atmos. Chem. Phys., 24, 10667–10687, https://doi.org/10.5194/acp-24-10667-2024, https://doi.org/10.5194/acp-24-10667-2024, 2024
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We investigated the characteristics of new particle formation (NPF) for various environments from urban background to high Alpine and the impacts of NPF on cloud condensation nuclei and aerosol radiative forcing. NPF features differ between site categories, implying the crucial role of local environmental factors such as the degree of emissions and meteorological conditions. The results also underscore the importance of local environments when assessing the impact of NPF on climate in models.
Baptiste Testa, Lukas Durdina, Jacinta Edebeli, Curdin Spirig, and Zamin A. Kanji
Atmos. Chem. Phys., 24, 10409–10424, https://doi.org/10.5194/acp-24-10409-2024, https://doi.org/10.5194/acp-24-10409-2024, 2024
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Aviation soot residuals released from contrails can become compacted upon sublimation of the ice crystals, generating new voids in the aggregates where ice nucleation can occur. Here we show that contrail-processed soot is highly compact but that it remains unable to form ice at a relative humidity different from that required for the formation of background cirrus from the more ubiquitous aqueous solution droplets, suggesting that it will not perturb cirrus cloud formation via ice nucleation.
Kunfeng Gao, Franziska Vogel, Romanos Foskinis, Stergios Vratolis, Maria I. Gini, Konstantinos Granakis, Anne-Claire Billault-Roux, Paraskevi Georgakaki, Olga Zografou, Prodromos Fetfatzis, Alexis Berne, Alexandros Papayannis, Konstantinos Eleftheridadis, Ottmar Möhler, and Athanasios Nenes
Atmos. Chem. Phys., 24, 9939–9974, https://doi.org/10.5194/acp-24-9939-2024, https://doi.org/10.5194/acp-24-9939-2024, 2024
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Ice nucleating particle (INP) concentrations are required for correct predictions of clouds and precipitation in a changing climate, but they are poorly constrained in climate models. We unravel source contributions to INPs in the eastern Mediterranean and find that biological particles are important, regardless of their origin. The parameterizations developed exhibit superior performance and enable models to consider biological-particle effects on INPs.
Alexandra Kuwano, Amato T. Evan, Blake Walkowiak, and Robert Frouin
Atmos. Chem. Phys., 24, 9843–9868, https://doi.org/10.5194/acp-24-9843-2024, https://doi.org/10.5194/acp-24-9843-2024, 2024
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The dust direct radiative effect is highly uncertain. Here we used new measurements collected over 3 years and during dust storms at a field site in a desert region in the southwestern United States to estimate the regional dust direct radiative effect. We also used novel soil mineralogy retrieved from an airborne spectrometer to estimate this parameter with model output. We find that, in this region, dust has a minimal net cooling effect on this region's climate.
Jutta Kesti, Ewan J. O'Connor, Anne Hirsikko, John Backman, Maria Filioglou, Anu-Maija Sundström, Juha Tonttila, Heikki Lihavainen, Hannele Korhonen, and Eija Asmi
Atmos. Chem. Phys., 24, 9369–9386, https://doi.org/10.5194/acp-24-9369-2024, https://doi.org/10.5194/acp-24-9369-2024, 2024
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The study combines aerosol particle measurements at the surface and vertical profiling of the atmosphere with a scanning Doppler lidar to investigate how particle transportation together with boundary layer evolution can affect particle and SO2 concentrations at the surface in the Arabian Peninsula region. The instrumentation enabled us to see elevated nucleation mode particle and SO2 concentrations at the surface when air masses transported from polluted areas are mixed in the boundary layer.
Jiangchuan Tao, Biao Luo, Weiqi Xu, Gang Zhao, Hanbin Xu, Biao Xue, Miaomiao Zhai, Wanyun Xu, Huarong Zhao, Sanxue Ren, Guangsheng Zhou, Li Liu, Ye Kuang, and Yele Sun
Atmos. Chem. Phys., 24, 9131–9154, https://doi.org/10.5194/acp-24-9131-2024, https://doi.org/10.5194/acp-24-9131-2024, 2024
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Using simultaneous measurements of DMA–CCNC, H(/V)TDMA, and DMA–SP2, impacts of primary emissions and secondary aerosol formations on changes in aerosol physicochemical properties were comprehensively investigated. It was found that intercomparisons among aerosol mixing-state parameters derived from different techniques can help us gain more insight into aerosol physical properties which, in turn, will aid the investigation of emission characteristics and secondary aerosol formation pathways.
Marco A. Franco, Rafael Valiati, Bruna A. Holanda, Bruno B. Meller, Leslie A. Kremper, Luciana V. Rizzo, Samara Carbone, Fernando G. Morais, Janaína P. Nascimento, Meinrat O. Andreae, Micael A. Cecchini, Luiz A. T. Machado, Milena Ponczek, Ulrich Pöschl, David Walter, Christopher Pöhlker, and Paulo Artaxo
Atmos. Chem. Phys., 24, 8751–8770, https://doi.org/10.5194/acp-24-8751-2024, https://doi.org/10.5194/acp-24-8751-2024, 2024
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The Amazon wet-season atmosphere was studied at the Amazon Tall Tower Observatory site, revealing vertical variations (between 60 and 325 m) in natural aerosols. Daytime mixing contrasted with nighttime stratification, with distinct rain-induced changes in aerosol populations. Notably, optical property recovery at higher levels was faster, while near-canopy aerosols showed higher scattering efficiency. These findings enhance our understanding of aerosol impacts on climate dynamics.
Lijing Chen, Lei Zhang, Yong She, Zhaoliang Zeng, Yu Zheng, Biao Tian, Wenqian Zhang, Zhaohui Liu, and Minghu Ding
EGUsphere, https://doi.org/10.5194/egusphere-2024-798, https://doi.org/10.5194/egusphere-2024-798, 2024
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AOD at Zhongshan Station varies seasonally, with lower values in summer and higher values in winter. Winter and spring AOD increases due to reduced fine mode particles, while summer and autumn increases are linked to particle growth. Duirnal AOD variation correlates positively with temperature but negatively with wind speed and humidity. Backward trajectory shows aerosols on high (low) AOD days primarily originate from the ocean (interior Antarctica).
Kristina Pistone, Eric M. Wilcox, Paquita Zuidema, Marco Giordano, James Podolske, Samuel E. LeBlanc, Meloë Kacenelenbogen, Steven G. Howell, and Steffen Freitag
Atmos. Chem. Phys., 24, 7983–8005, https://doi.org/10.5194/acp-24-7983-2024, https://doi.org/10.5194/acp-24-7983-2024, 2024
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The springtime southeast Atlantic atmosphere contains lots of smoke from continental fires. This smoke travels with water vapor; more smoke means more humidity. We use aircraft observations and models to describe how the values change through the season and over the region. We sort the atmosphere into different types by vertical structure and amount of smoke and humidity. Since our work shows how frequently these components coincide, it helps to better quantify heating effects over this region.
Julika Zinke, Gabriel Freitas, Rachel Ann Foster, Paul Zieger, Ernst Douglas Nilsson, Piotr Markuszewski, and Matthew Edward Salter
EGUsphere, https://doi.org/10.5194/egusphere-2024-1851, https://doi.org/10.5194/egusphere-2024-1851, 2024
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Bioaerosols, which can influence climate and human health, were studied in the Baltic Sea. In May and August 2021, we used a sea spray simulation chamber on two ship based campaigns to collect and measure these aerosols. We found that bacteria were enriched in the air compared to seawater. Bacterial diversity was analyzed using DNA sequencing. Our methods provided consistent estimates of bacterial emission fluxes, aligning with previous studies.
Yange Deng, Hiroshi Tanimoto, Kohei Ikeda, Sohiko Kameyama, Sachiko Okamoto, Jinyoung Jung, Young Jun Yoon, Eun Jin Yang, and Sung-Ho Kang
Atmos. Chem. Phys., 24, 6339–6357, https://doi.org/10.5194/acp-24-6339-2024, https://doi.org/10.5194/acp-24-6339-2024, 2024
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Black carbon (BC) aerosols play important roles in Arctic climate change, yet they are not well understood because of limited observational data. We observed BC mass concentrations (mBC) in the western Arctic Ocean during summer and early autumn 2016–2020. The mean mBC in 2019 was much higher than in other years. Biomass burning was likely the dominant BC source. Boreal fire BC transport occurring near the surface and/or in the mid-troposphere contributed to high-BC events in the Arctic Ocean.
Erin N. Raif, Sarah L. Barr, Mark D. Tarn, James B. McQuaid, Martin I. Daily, Steven J. Abel, Paul A. Barrett, Keith N. Bower, Paul R. Field, Kenneth S. Carslaw, and Benjamin J. Murray
EGUsphere, https://doi.org/10.5194/egusphere-2024-1502, https://doi.org/10.5194/egusphere-2024-1502, 2024
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Ice-nucleating particles (INPs) allow ice to form in clouds at temperatures warmer than -35°C. We measured INP concentrations over the Norwegian and Barents seas in weather events where cold air is ejected from the Arctic. These concentrations were among the highest measured in the Arctic and it is likely that the INPs were transported to the Arctic from distant regions. These results show it is important to consider hemispheric-scale INP processes to understand INP concentrations in the Arctic.
Fernando Rejano, Andrea Casans, Marta Via, Juan Andrés Casquero-Vera, Sonia Castillo, Hassan Lyamani, Alberto Cazorla, Elisabeth Andrews, Daniel Pérez-Ramírez, Andrés Alastuey, Francisco Javier Gómez-Moreno, Lucas Alados-Arboledas, Francisco José Olmo, and Gloria Titos
EGUsphere, https://doi.org/10.5194/egusphere-2024-1059, https://doi.org/10.5194/egusphere-2024-1059, 2024
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This study provides valuable insights to improve cloud condensation nuclei (CCN) estimations at a high-altitude remote site which is influenced by nearby urban pollution. Understanding the factors that affect CCN estimations is essential to improve the CCN data coverage worldwide and assess aerosol-cloud interactions in a global scale. This is crucial for improving climate models since aerosol-cloud interactions are the most important source of uncertainty in climate projections.
Máté Vörösmarty, Philip K. Hopke, and Imre Salma
Atmos. Chem. Phys., 24, 5695–5712, https://doi.org/10.5194/acp-24-5695-2024, https://doi.org/10.5194/acp-24-5695-2024, 2024
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The World Health Organization identified ultrafine particles, which make up most of the particle number concentrations, as a potential risk factor for humans. The sources of particle numbers are very different from those of the particulate matter mass. We performed source apportionment of size-segregated particle number concentrations over the diameter range of 6–1000 nm in Budapest for 11 full years. Six source types were identified, characterized and quantified.
Jerome D. Fast, Adam C. Varble, Fan Mei, Mikhail Pekour, Jason Tomlinson, Alla Zelenyuk, Art J. Sedlacek III, Maria Zawadowicz, and Louisa K. Emmons
EGUsphere, https://doi.org/10.5194/egusphere-2024-1349, https://doi.org/10.5194/egusphere-2024-1349, 2024
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Aerosol property measurements recently collected at the ground and by a research aircraft in central Argentina during the CACTI campaign exhibit large spatial and temporal variability. These measurements coupled with coincident meteorological information provide a valuable dataset needed to evaluate and improve model predictions of aerosols in a traditionally data sparse region of South America.
Gabriel Pereira Freitas, Ben Kopec, Kouji Adachi, Radovan Krejci, Dominic Heslin-Rees, Karl Espen Yttri, Alun Hubbard, Jeffrey M. Welker, and Paul Zieger
Atmos. Chem. Phys., 24, 5479–5494, https://doi.org/10.5194/acp-24-5479-2024, https://doi.org/10.5194/acp-24-5479-2024, 2024
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Bioaerosols can participate in ice formation within clouds. In the Arctic, where global warming manifests most, they may become more important as their sources prevail for longer periods of the year. We have directly measured bioaerosols within clouds for a full year at an Arctic mountain site using a novel combination of cloud particle sampling and single-particle techniques. We show that bioaerosols act as cloud seeds and may influence the presence of ice within clouds.
Andreas Petzold, Ulrich Bundke, Anca Hienola, Paolo Laj, Cathrine Lund Myhre, Alex Vermeulen, Angeliki Adamaki, Werner Kutsch, Valerie Thouret, Damien Boulanger, Markus Fiebig, Markus Stocker, Zhiming Zhao, and Ari Asmi
Atmos. Chem. Phys., 24, 5369–5388, https://doi.org/10.5194/acp-24-5369-2024, https://doi.org/10.5194/acp-24-5369-2024, 2024
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Easy and fast access to long-term and high-quality observational data is recognised as fundamental to environmental research and the development of climate forecasting and assessment services. We discuss the potential new directions in atmospheric sciences offered by the atmosphere-centric European research infrastructures ACTRIS, IAGOS, and ICOS, building on their capabilities for standardised provision of data through open access combined with tools and methods of data-intensive science.
Elise K. Wilbourn, Larissa Lacher, Carlos Guerrero, Hemanth S. K. Vepuri, Kristina Höhler, Jens Nadolny, Aidan D. Pantoya, Ottmar Möhler, and Naruki Hiranuma
Atmos. Chem. Phys., 24, 5433–5456, https://doi.org/10.5194/acp-24-5433-2024, https://doi.org/10.5194/acp-24-5433-2024, 2024
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Ambient ice particles were measured at terrestrial and temperate marine sites. Ice particles were more abundant in the former site, while the fraction of ice particles relative to total ambient particles, representing atmospheric ice nucleation efficiency, was higher in the latter site. Ice nucleation parameterizations were developed as a function of examined freezing temperatures from two sites for our study periods (autumn).
Ping Tian, Dantong Liu, Kang Hu, Yangzhou Wu, Mengyu Huang, Hui He, Jiujiang Sheng, Chenjie Yu, Dawei Hu, and Deping Ding
Atmos. Chem. Phys., 24, 5149–5164, https://doi.org/10.5194/acp-24-5149-2024, https://doi.org/10.5194/acp-24-5149-2024, 2024
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The results provide direct evidence of efficient droplet activation of black carbon (BC). The cloud condensation nuclei (CCN) activation fraction of BC was higher than for all particles, suggesting higher CCN activity of BC, even though its hygroscopicity is lower. Our research reveals that the evolution of BC's hygroscopicity and its CCN activation properties through atmospheric aging can be effectively characterized by the photochemical age.
Henriette Gebauer, Athena Augusta Floutsi, Moritz Haarig, Martin Radenz, Ronny Engelmann, Dietrich Althausen, Annett Skupin, Albert Ansmann, Cordula Zenk, and Holger Baars
Atmos. Chem. Phys., 24, 5047–5067, https://doi.org/10.5194/acp-24-5047-2024, https://doi.org/10.5194/acp-24-5047-2024, 2024
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Sulfate aerosol from the volcanic eruption at La Palma in 2021 was observed over Cabo Verde. We characterized the aerosol burden based on a case study of lidar and sun photometer observations. We compared the volcanic case to the typical background conditions (reference case) to quantify the volcanic pollution. We show the first ever measurements of the extinction coefficient, lidar ratio and depolarization ratio at 1064 nm for volcanic sulfate.
Cyrille Flamant, Jean-Pierre Chaboureau, Marco Gaetani, Kerstin Schepanski, and Paola Formenti
Atmos. Chem. Phys., 24, 4265–4288, https://doi.org/10.5194/acp-24-4265-2024, https://doi.org/10.5194/acp-24-4265-2024, 2024
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In the austral dry season, the atmospheric composition over southern Africa is dominated by biomass burning aerosols and terrigenous aerosols (so-called mineral dust). This study suggests that the radiative effect of biomass burning aerosols needs to be taken into account to properly forecast dust emissions in Namibia.
Boming Liu, Xin Ma, Jianping Guo, Renqiang Wen, Hui Li, Shikuan Jin, Yingying Ma, Xiaoran Guo, and Wei Gong
Atmos. Chem. Phys., 24, 4047–4063, https://doi.org/10.5194/acp-24-4047-2024, https://doi.org/10.5194/acp-24-4047-2024, 2024
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Accurate wind profile estimation, especially for the lowest few hundred meters of the atmosphere, is of great significance for the weather, climate, and renewable energy sector. We propose a novel method that combines the power-law method with the random forest algorithm to extend wind profiles beyond the surface layer. Compared with the traditional algorithm, this method has better stability and spatial applicability and can be used to obtain the wind profiles on different land cover types.
Gabriela R. Unfer, Luiz A. T. Machado, Paulo Artaxo, Marco A. Franco, Leslie A. Kremper, Mira L. Pöhlker, Ulrich Pöschl, and Christopher Pöhlker
Atmos. Chem. Phys., 24, 3869–3882, https://doi.org/10.5194/acp-24-3869-2024, https://doi.org/10.5194/acp-24-3869-2024, 2024
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Amazonian aerosols and their interactions with precipitation were studied by understanding them in a 3D space based on three parameters that characterize the concentration and size distribution of aerosols. The results showed characteristic arrangements regarding seasonal and diurnal cycles, as well as when interacting with precipitation. The use of this 3D space appears to be a promising tool for aerosol population analysis and for model validation and parameterization.
Anil Kumar Mandariya, Ajit Ahlawat, Mohammed Haneef, Nisar Ali Baig, Kanan Patel, Joshua Apte, Lea Hildebrandt Ruiz, Alfred Wiedensohler, and Gazala Habib
Atmos. Chem. Phys., 24, 3627–3647, https://doi.org/10.5194/acp-24-3627-2024, https://doi.org/10.5194/acp-24-3627-2024, 2024
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The current study explores the temporal variation of size-selected particle hygroscopicity in Delhi for the first time. Here, we report that the high volume fraction contribution of ammonium chloride to aerosol governs the high aerosol hygroscopicity and associated liquid water content based on the experimental data. The episodically high ammonium chloride present in Delhi's atmosphere could lead to haze and fog formation under high relative humidity in the region.
Yueyue Cheng, Chao Liu, Jiandong Wang, Jiaping Wang, Zhouyang Zhang, Li Chen, Dafeng Ge, Caijun Zhu, Jinbo Wang, and Aijun Ding
Atmos. Chem. Phys., 24, 3065–3078, https://doi.org/10.5194/acp-24-3065-2024, https://doi.org/10.5194/acp-24-3065-2024, 2024
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Brown carbon (BrC), a light-absorbing aerosol, plays a pivotal role in influencing global climate. However, assessing BrC radiative effects remains challenging because the required observational data are hardly accessible. Here we develop a new BrC radiative effect estimation method combining conventional observations and numerical models. Our findings reveal that BrC absorbs up to a third of the sunlight at 370 nm that black carbon does, highlighting its importance in aerosol radiative effects.
Larissa Lacher, Michael P. Adams, Kevin Barry, Barbara Bertozzi, Heinz Bingemer, Cristian Boffo, Yannick Bras, Nicole Büttner, Dimitri Castarede, Daniel J. Cziczo, Paul J. DeMott, Romy Fösig, Megan Goodell, Kristina Höhler, Thomas C. J. Hill, Conrad Jentzsch, Luis A. Ladino, Ezra J. T. Levin, Stephan Mertes, Ottmar Möhler, Kathryn A. Moore, Benjamin J. Murray, Jens Nadolny, Tatjana Pfeuffer, David Picard, Carolina Ramírez-Romero, Mickael Ribeiro, Sarah Richter, Jann Schrod, Karine Sellegri, Frank Stratmann, Benjamin E. Swanson, Erik S. Thomson, Heike Wex, Martin J. Wolf, and Evelyn Freney
Atmos. Chem. Phys., 24, 2651–2678, https://doi.org/10.5194/acp-24-2651-2024, https://doi.org/10.5194/acp-24-2651-2024, 2024
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Aerosol particles that trigger ice formation in clouds are important for the climate system but are very rare in the atmosphere, challenging measurement techniques. Here we compare three cloud chambers and seven methods for collecting aerosol particles on filters for offline analysis at a mountaintop station. A general good agreement of the methods was found when sampling aerosol particles behind a whole air inlet, supporting their use for obtaining data that can be implemented in models.
Andrea Cuesta-Mosquera, Kristina Glojek, Griša Močnik, Luka Drinovec, Asta Gregorič, Martin Rigler, Matej Ogrin, Baseerat Romshoo, Kay Weinhold, Maik Merkel, Dominik van Pinxteren, Hartmut Herrmann, Alfred Wiedensohler, Mira Pöhlker, and Thomas Müller
Atmos. Chem. Phys., 24, 2583–2605, https://doi.org/10.5194/acp-24-2583-2024, https://doi.org/10.5194/acp-24-2583-2024, 2024
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This study evaluated the air pollution and climate impacts of residential-wood-burning particle emissions from a rural European site. The authors investigate the optical and physical properties that connect the aerosol emissions with climate by evaluating atmospheric radiative impacts via simple-forcing calculations. The study contributes to reducing the lack of information on the understanding of the optical properties of air pollution from anthropogenic sources.
Xiangxinyue Meng, Zhijun Wu, Jingchuan Chen, Yanting Qiu, Taomou Zong, Mijung Song, Jiyi Lee, and Min Hu
Atmos. Chem. Phys., 24, 2399–2414, https://doi.org/10.5194/acp-24-2399-2024, https://doi.org/10.5194/acp-24-2399-2024, 2024
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Our study revealed that particles predominantly exist in a semi-solid or solid state during clean winter days with RH below 30 %. However, a non-liquid to a liquid phase transition occurred when the aerosol liquid water (ALW) mass fraction surpassed 15 % (dry mass) at transition RH thresholds ranging from 40 % to 60 %. We also provide insights into the increasingly important roles of particle phase state variation and ALW in secondary particulate growth during haze formation in Beijing, China.
Bighnaraj Sarangi, Darrel Baumgardner, Ana Isabel Calvo, Benjamin Bolaños-Rosero, Roberto Fraile, Alberto Rodríguez-Fernández, Delia Fernández-González, Carlos Blanco-Alegre, Cátia Gonçalves, Estela D. Vicente, and Olga L. Mayol Bracero
EGUsphere, https://doi.org/10.5194/egusphere-2024-446, https://doi.org/10.5194/egusphere-2024-446, 2024
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Measurements of fluorescing aerosol particle properties have been made during two major African dust events, one over the island of Puerto Rico and the other over the city of León, Spain The measurements were with two Wideband Integrated Bioaerosol Spectrometers. A significant change in the background aerosol properties, at both locations, is observed when the dust is in the respective regions.
Yiming Wang, Haolin Wang, Yujie Qin, Xinqi Xu, Guowen He, Nanxi Liu, Shengjie Miao, Xiao Lu, Haichao Wang, and Shaojia Fan
Atmos. Chem. Phys., 24, 2267–2285, https://doi.org/10.5194/acp-24-2267-2024, https://doi.org/10.5194/acp-24-2267-2024, 2024
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We conducted a vertical measurement of winter PM2.5 using a mobile multi-lidar system in four cities. Combined with the surface PM2.5 data, the ERA5 reanalysis data, and GEOS-Chem simulations during Dec 2018–Feb 2019, we found that transport nocturnal PM2.5 enhancement by subsidence (T-NPES) events widely occurred with high frequencies in plains regions in eastern China but happened less often in basin regions like Xi’an and Chengdu. We propose a conceptual model of the T-NPES events.
Dominic Heslin-Rees, Peter Tunved, Johan Ström, Roxana Cremer, Paul Zieger, Ilona Riipinen, Annica M. L. Ekman, Konstantinos Eleftheriadis, and Radovan Krejci
Atmos. Chem. Phys., 24, 2059–2075, https://doi.org/10.5194/acp-24-2059-2024, https://doi.org/10.5194/acp-24-2059-2024, 2024
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Light-absorbing atmospheric particles (e.g. black carbon – BC) exert a warming effect on the Arctic climate. We show that the amount of particle light absorption decreased from 2002 to 2023. We conclude that in addition to reductions in emissions of BC, wet removal plays a role in the long-term reduction of BC in the Arctic, given the increase in surface precipitation experienced by air masses arriving at the site. The potential impact of biomass burning events is shown to have increased.
Julika Zinke, Ernst Douglas Nilsson, Piotr Markuszewski, Paul Zieger, Eva Monica Mårtensson, Anna Rutgersson, Erik Nilsson, and Matthew Edward Salter
Atmos. Chem. Phys., 24, 1895–1918, https://doi.org/10.5194/acp-24-1895-2024, https://doi.org/10.5194/acp-24-1895-2024, 2024
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We conducted two research campaigns in the Baltic Sea, during which we combined laboratory sea spray simulation experiments with flux measurements on a nearby island. To combine these two methods, we scaled the laboratory measurements to the flux measurements using three different approaches. As a result, we derived a parameterization that is dependent on wind speed and wave state for particles with diameters 0.015–10 μm. This parameterization is applicable to low-salinity waters.
Sarah Tinorua, Cyrielle Denjean, Pierre Nabat, Thierry Bourrianne, Véronique Pont, François Gheusi, and Emmanuel Leclerc
Atmos. Chem. Phys., 24, 1801–1824, https://doi.org/10.5194/acp-24-1801-2024, https://doi.org/10.5194/acp-24-1801-2024, 2024
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At a French high-altitude site, where many complex interactions between black carbon (BC), radiation, clouds and snow impact climate, 2 years of refractive BC (rBC) and aerosol optical and microphysical measurements have been made. We observed strong seasonal rBC properties variations, with an enhanced absorption in summer compared to winter. The combination of rBC emission sources, transport pathways, atmospheric dynamics and chemical processes explains the rBC light absorption seasonality.
Wenwen Ma, Rong Sun, Xiaoping Wang, Zheng Zong, Shizhen Zhao, Zeyu Sun, Chongguo Tian, Jianhui Tang, Song Cui, Jun Li, and Gan Zhang
Atmos. Chem. Phys., 24, 1509–1523, https://doi.org/10.5194/acp-24-1509-2024, https://doi.org/10.5194/acp-24-1509-2024, 2024
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This is the first report of long-term atmospheric PAH monitoring around the Bohai Sea. The results showed that the concentrations of PAHs in the atmosphere around the Bohai Sea decreased from June 2014 to May 2019, especially the concentrations of highly toxic PAHs. This indicates that the contributions from PAH sources changed to a certain extent in different areas, and it also led to reductions in the related health risk and medical costs following pollution prevention and control.
Mary C. Robinson, Kaitlin Schueth, and Karin Ardon-Dryer
EGUsphere, https://doi.org/10.5194/egusphere-2024-113, https://doi.org/10.5194/egusphere-2024-113, 2024
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On February 26, 2023, New Mexico and West Texas were impacted by a severe dust storm. 21 meteorological stations and 19 PM2.5 and PM10 stations were used to analyze this dust storm. Dust articles were in the air for 18 hours, and dust storm conditions lasted up to 65 minutes. Hourly PM2.5 and PM10 concentrations were up to 518.4 and 9,983 µg m-3, respectively. For Lubbock, Texas the maximum PM2.5 concentrations were the highest ever recorded.
Silke Groß, Volker Freudenthaler, Moritz Haarig, Albert Ansmann, Carlos Toledano, David Mateos, Petra Seibert, Rodanthi-Elisavet Mamouri, Argyro Nisantzi, Josef Gasteiger, Maximilian Dollner, Anne Tipka, Manuel Schöberl, Marilena Teri, and Bernadett Weinzierl
EGUsphere, https://doi.org/10.5194/egusphere-2024-140, https://doi.org/10.5194/egusphere-2024-140, 2024
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Aerosols contribute to the largest uncertainties in climate change predictions. Especially absorbing aerosols propose difficulties in our understanding. The eastern Mediterranean is a hot spot for aerosols with natural and anthropogenic contributions. We present lidar measurements performed during the A-LIFE field experiment to characterize aerosols and aerosol mixtures. We extend current classification and separation schemes and compare different classification schemes.
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Short summary
The paper presents aerosol properties measured during the Cloud Aerosol Radiative Forcing Experiment (CARDEX) on the Maldives Islands in winter 2012. The vertical distribution of absorbing aerosol which is very relevant to the radiative forcing in that region, is investigated. A method for determining particle absorption and equivalent black carbon concentration from lidar extinction coefficients, characteristic single scattering albedo and mass absorption efficiency, is presented and evaluated.
The paper presents aerosol properties measured during the Cloud Aerosol Radiative Forcing...
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