Articles | Volume 18, issue 12
https://doi.org/10.5194/acp-18-8571-2018
© Author(s) 2018. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/acp-18-8571-2018
© Author(s) 2018. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Research article
| 
18 Jun 2018
Research article |
| 18 Jun 2018
| 18 Jun 2018
High summertime aerosol organic functional group concentrations from marine and seabird sources at Ross Island, Antarctica, during AWARE
Scripps Institution of Oceanography, University of California, San Diego,
9500 Gilman Drive, La Jolla, CA 92093, USA
Jeramy Dedrick
Scripps Institution of Oceanography, University of California, San Diego,
9500 Gilman Drive, La Jolla, CA 92093, USA
now at: Texas A&M University, 400 Bizzell St, College Station, TX 77843, USA
Scripps Institution of Oceanography, University of California, San Diego,
9500 Gilman Drive, La Jolla, CA 92093, USA
Gunnar I. Senum
Environmental & Climate Sciences Department, Brookhaven National
Laboratory, Building 815-E, Upton, NY 11973-5000, USA
Janek Uin
Environmental & Climate Sciences Department, Brookhaven National
Laboratory, Building 815-E, Upton, NY 11973-5000, USA
Chongai Kuang
Environmental & Climate Sciences Department, Brookhaven National
Laboratory, Building 815-E, Upton, NY 11973-5000, USA
Stephen R. Springston
Environmental & Climate Sciences Department, Brookhaven National
Laboratory, Building 815-E, Upton, NY 11973-5000, USA
W. Richard Leaitch
Environment and Climate Change Canada (ECCC), Toronto, ON, Canada
Allison C. Aiken
Earth and Environmental Science, Earth Systems Observations, Los Alamos
National Laboratory, Los Alamos, New Mexico, USA
Dan Lubin
Scripps Institution of Oceanography, University of California, San Diego,
9500 Gilman Drive, La Jolla, CA 92093, USA
Related authors
W. Richard Leaitch, Lynn M. Russell, Jun Liu, Felicia Kolonjari, Desiree Toom, Lin Huang, Sangeeta Sharma, Alina Chivulescu, Dan Veber, and Wendy Zhang
Atmos. Chem. Phys., 18, 3269–3287, https://doi.org/10.5194/acp-18-3269-2018, https://doi.org/10.5194/acp-18-3269-2018, 2018
Short summary
Short summary
Over 2 years of atmospheric aerosol organic functional group and microphysics measurements at the world's northernmost land observatory offer a unique high-latitude dataset. Lower organic mass (OM) concentrations and higher OM fractions accompany smaller particles during summer, with opposite results during winter to spring. Seasonally, the OM oxidation level is highest in winter, associated with primary marine alcohol groups. In summer, secondary processes dominate the marine influence on OM.
Alex K. Y. Lee, Chia-Li Chen, Jun Liu, Derek J. Price, Raghu Betha, Lynn M. Russell, Xiaolu Zhang, and Christopher D. Cappa
Atmos. Chem. Phys., 17, 15055–15067, https://doi.org/10.5194/acp-17-15055-2017, https://doi.org/10.5194/acp-17-15055-2017, 2017
Short summary
Short summary
Understanding the mixing state of ambient black carbon (BC) and the chemical characteristics of its associated coatings is important to evaluate BC fate and environmental impacts. This study reports fresh secondary organic aerosol (SOA) formation near traffic emissions during daytime. Our observations suggest that BC was unlikely the major condensation sink of SOA, and a portion of SOA condensed on BC surface was chemically different from other SOA particles that were externally mixed with BC.
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
Short summary
Short summary
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.
Karam Mansour, Stefano Decesari, Darius Ceburnis, Jurgita Ovadnevaite, Lynn M. Russell, Marco Paglione, Laurent Poulain, Shan Huang, Colin O'Dowd, and Matteo Rinaldi
Earth Syst. Sci. Data, 16, 2717–2740, https://doi.org/10.5194/essd-16-2717-2024, https://doi.org/10.5194/essd-16-2717-2024, 2024
Short summary
Short summary
We propose and evaluate machine learning predictive algorithms to model freshly formed biogenic methanesulfonic acid and sulfate concentrations. The long-term constructed dataset covers the North Atlantic at an unprecedented resolution. The improved parameterization of biogenic sulfur aerosols at regional scales is essential for determining their radiative forcing, which could help further understand marine-aerosol–cloud interactions and reduce uncertainties in climate models
Kristopher Scarci, Ryan C. Scott, Madison L. Ghiz, Andrew M. Vogelmann, and Dan Lubin
Atmos. Chem. Phys., 24, 6681–6697, https://doi.org/10.5194/acp-24-6681-2024, https://doi.org/10.5194/acp-24-6681-2024, 2024
Short summary
Short summary
We demonstrate what can be learned about an Antarctic region's climate from basic atmospheric irradiance measurements made by broadband and filter radiometers, instruments suitable for deployment at very remote sites, assisted by meteorological reanalysis and satellite remote sensing. Analysis of shortwave and longwave irradiance reveals subtle contrasts between meteorological regimes favoring cloud ice versus liquid water, relevant to onset versus inhibition of surface melt over ice shelves.
Israel Silber, Jennifer M. Comstock, Michael R. Kieburtz, and Lynn M. Russell
Earth Syst. Sci. Data Discuss., https://doi.org/10.5194/essd-2024-127, https://doi.org/10.5194/essd-2024-127, 2024
Revised manuscript accepted for ESSD
Short summary
Short summary
We present ARMTRAJ, a set of multi-purpose trajectory datasets generated using HYSPLIT informed by ERA5 reanalysis at 0.25° resolution, which augments cloud, aerosol, and boundary layer studies utilizing the U.S. DOE ARM data. ARMTRAJ data include ensemble run statistics that enhance consistency and serve as uncertainty metrics for airmass coordinates and state variables. ARMTRAJ is expected to become a near real-time product that will accompany past, ongoing, and future ARM deployments.
Emily Y. Li, Amir Yazdani, Ann M. Dillner, Guofeng Shen, Wyatt M. Champion, James J. Jetter, William T. Preston, Lynn M. Russell, Michael D. Hays, and Satoshi Takahama
Atmos. Meas. Tech., 17, 2401–2413, https://doi.org/10.5194/amt-17-2401-2024, https://doi.org/10.5194/amt-17-2401-2024, 2024
Short summary
Short summary
Infrared spectroscopy is a cost-effective measurement technique to characterize the chemical composition of organic aerosol emissions. This technique differentiates the organic matter emission factor from different fuel sources by their characteristic functional groups. Comparison with collocated measurements suggests that polycyclic aromatic hydrocarbon concentrations in emissions estimated by conventional chromatography may be substantially underestimated.
Ryan N. Farley, James E. Lee, Laura-Hélèna Rivellini, Alex K. Y. Lee, Rachael Dal Porto, Christopher D. Cappa, Kyle Gorkowski, Abu Sayeed Md Shawon, Katherine B. Benedict, Allison C. Aiken, Manvendra K. Dubey, and Qi Zhang
Atmos. Chem. Phys., 24, 3953–3971, https://doi.org/10.5194/acp-24-3953-2024, https://doi.org/10.5194/acp-24-3953-2024, 2024
Short summary
Short summary
The black carbon aerosol composition and mixing state were characterized using a soot particle aerosol mass spectrometer. Single-particle measurements revealed the major role of atmospheric processing in modulating the black carbon mixing state. A significant fraction of soot particles were internally mixed with oxidized organic aerosol and sulfate, with implications for activation as cloud nuclei.
Ryan N. Farley, Sonya Collier, Christopher D. Cappa, Leah R. Williams, Timothy B. Onasch, Lynn M. Russell, Hwajin Kim, and Qi Zhang
Atmos. Chem. Phys., 23, 15039–15056, https://doi.org/10.5194/acp-23-15039-2023, https://doi.org/10.5194/acp-23-15039-2023, 2023
Short summary
Short summary
Soot particles, also known as black carbon (BC), have important implications for global climate and regional air quality. After the particles are emitted, BC can be coated with other material, impacting the aerosol properties. We selectively measured the composition of particles containing BC to explore their sources and chemical transformations in the atmosphere. We focus on a persistent, multiday fog event in order to study the effects of chemical reactions occurring within liquid droplets.
Calvin Howes, Pablo E. Saide, Hugh Coe, Amie Dobracki, Steffen Freitag, Jim M. Haywood, Steven G. Howell, Siddhant Gupta, Janek Uin, Mary Kacarab, Chongai Kuang, L. Ruby Leung, Athanasios Nenes, Greg M. McFarquhar, James Podolske, Jens Redemann, Arthur J. Sedlacek, Kenneth L. Thornhill, Jenny P. S. Wong, Robert Wood, Huihui Wu, Yang Zhang, Jianhao Zhang, and Paquita Zuidema
Atmos. Chem. Phys., 23, 13911–13940, https://doi.org/10.5194/acp-23-13911-2023, https://doi.org/10.5194/acp-23-13911-2023, 2023
Short summary
Short summary
To better understand smoke properties and its interactions with clouds, we compare the WRF-CAM5 model with observations from ORACLES, CLARIFY, and LASIC field campaigns in the southeastern Atlantic in August 2017. The model transports and mixes smoke well but does not fully capture some important processes. These include smoke chemical and physical aging over 4–12 days, smoke removal by rain, sulfate particle formation, aerosol activation into cloud droplets, and boundary layer turbulence.
Amie Dobracki, Paquita Zuidema, Steven G. Howell, Pablo Saide, Steffen Freitag, Allison C. Aiken, Sharon P. Burton, Arthur J. Sedlacek III, Jens Redemann, and Robert Wood
Atmos. Chem. Phys., 23, 4775–4799, https://doi.org/10.5194/acp-23-4775-2023, https://doi.org/10.5194/acp-23-4775-2023, 2023
Short summary
Short summary
Southern Africa produces approximately one-third of the world’s carbon from fires. The thick smoke layer can flow westward, interacting with the southeastern Atlantic cloud deck. The net radiative impact can alter regional circulation patterns, impacting rainfall over Africa. We find that the smoke is highly absorbing of sunlight, mostly because it contains more black carbon than smoke over the Northern Hemisphere.
Francesca Gallo, Janek Uin, Kevin J. Sanchez, Richard H. Moore, Jian Wang, Robert Wood, Fan Mei, Connor Flynn, Stephen Springston, Eduardo B. Azevedo, Chongai Kuang, and Allison C. Aiken
Atmos. Chem. Phys., 23, 4221–4246, https://doi.org/10.5194/acp-23-4221-2023, https://doi.org/10.5194/acp-23-4221-2023, 2023
Short summary
Short summary
This study provides a summary statistic of multiday aerosol plume transport event influences on aerosol physical properties and the cloud condensation nuclei budget at the U.S. Department of Energy Atmospheric Radiation Measurement Facility in the eastern North Atlantic (ENA). An algorithm that integrates aerosol properties is developed and applied to identify multiday aerosol transport events. The influence of the aerosol plumes on aerosol populations at the ENA is successively assessed.
Veronica Z. Berta, Lynn M. Russell, Derek J. Price, Chia-Li Chen, Alex K. Y. Lee, Patricia K. Quinn, Timothy S. Bates, Thomas G. Bell, and Michael J. Behrenfeld
Atmos. Chem. Phys., 23, 2765–2787, https://doi.org/10.5194/acp-23-2765-2023, https://doi.org/10.5194/acp-23-2765-2023, 2023
Short summary
Short summary
Amines are compounds emitted from a variety of marine and continental sources and were measured by aerosol mass spectrometry and Fourier transform infrared spectroscopy during the North Atlantic Aerosols and Marine Ecosystems Study (NAAMES) cruises. Secondary continental and primary marine sources of amines were identified by comparisons to tracers. The results show that the two methods are complementary for investigating amines in the marine environment.
Francesca Gallo, Kevin J. Sanchez, Bruce E. Anderson, Ryan Bennett, Matthew D. Brown, Ewan C. Crosbie, Chris Hostetler, Carolyn Jordan, Melissa Yang Martin, Claire E. Robinson, Lynn M. Russell, Taylor J. Shingler, Michael A. Shook, Kenneth L. Thornhill, Elizabeth B. Wiggins, Edward L. Winstead, Armin Wisthaler, Luke D. Ziemba, and Richard H. Moore
Atmos. Chem. Phys., 23, 1465–1490, https://doi.org/10.5194/acp-23-1465-2023, https://doi.org/10.5194/acp-23-1465-2023, 2023
Short summary
Short summary
We integrate in situ ship- and aircraft-based measurements of aerosol, trace gases, and meteorological parameters collected during the NASA North Atlantic Aerosols and Marine Ecosystems Study (NAAMES) field campaigns in the western North Atlantic Ocean region. A comprehensive characterization of the vertical profiles of aerosol properties under different seasonal regimes is provided for improving the understanding of aerosol key processes and aerosol–cloud interactions in marine regions.
Paul A. Barrett, Steven J. Abel, Hugh Coe, Ian Crawford, Amie Dobracki, James Haywood, Steve Howell, Anthony Jones, Justin Langridge, Greg M. McFarquhar, Graeme J. Nott, Hannah Price, Jens Redemann, Yohei Shinozuka, Kate Szpek, Jonathan W. Taylor, Robert Wood, Huihui Wu, Paquita Zuidema, Stéphane Bauguitte, Ryan Bennett, Keith Bower, Hong Chen, Sabrina Cochrane, Michael Cotterell, Nicholas Davies, David Delene, Connor Flynn, Andrew Freedman, Steffen Freitag, Siddhant Gupta, David Noone, Timothy B. Onasch, James Podolske, Michael R. Poellot, Sebastian Schmidt, Stephen Springston, Arthur J. Sedlacek III, Jamie Trembath, Alan Vance, Maria A. Zawadowicz, and Jianhao Zhang
Atmos. Meas. Tech., 15, 6329–6371, https://doi.org/10.5194/amt-15-6329-2022, https://doi.org/10.5194/amt-15-6329-2022, 2022
Short summary
Short summary
To better understand weather and climate, it is vital to go into the field and collect observations. Often measurements take place in isolation, but here we compared data from two aircraft and one ground-based site. This was done in order to understand how well measurements made on one platform compared to those made on another. Whilst this is easy to do in a controlled laboratory setting, it is more challenging in the real world, and so these comparisons are as valuable as they are rare.
Joshin Kumar, Theo Paik, Nishit J. Shetty, Patrick Sheridan, Allison C. Aiken, Manvendra K. Dubey, and Rajan K. Chakrabarty
Atmos. Meas. Tech., 15, 4569–4583, https://doi.org/10.5194/amt-15-4569-2022, https://doi.org/10.5194/amt-15-4569-2022, 2022
Short summary
Short summary
Accurate long-term measurement of aerosol light absorption is vital for assessing direct aerosol radiative forcing. Light absorption by aerosols at the US Department of Energy long-term climate monitoring SGP site is measured using the Particle Soot Absorption Photometer (PSAP), which suffers from artifacts and biases difficult to quantify. Machine learning offers a promising path forward to correct for biases in the long-term absorption dataset at the SGP site and similar Class-I areas.
Jeramy L. Dedrick, Georges Saliba, Abigail S. Williams, Lynn M. Russell, and Dan Lubin
Atmos. Meas. Tech., 15, 4171–4194, https://doi.org/10.5194/amt-15-4171-2022, https://doi.org/10.5194/amt-15-4171-2022, 2022
Short summary
Short summary
A new method is presented to retrieve the sea spray aerosol size distribution by combining submicron size and nephelometer scattering based on Mie theory. Using available sea spray tracers, we find that this approach serves as a comparable substitute to supermicron size distribution measurements, which are limited in availability at marine sites. Application of this technique can expand sea spray observations and improve the characterization of marine aerosol impacts on clouds and climate.
Kevin J. Sanchez, Bo Zhang, Hongyu Liu, Matthew D. Brown, Ewan C. Crosbie, Francesca Gallo, Johnathan W. Hair, Chris A. Hostetler, Carolyn E. Jordan, Claire E. Robinson, Amy Jo Scarino, Taylor J. Shingler, Michael A. Shook, Kenneth L. Thornhill, Elizabeth B. Wiggins, Edward L. Winstead, Luke D. Ziemba, Georges Saliba, Savannah L. Lewis, Lynn M. Russell, Patricia K. Quinn, Timothy S. Bates, Jack Porter, Thomas G. Bell, Peter Gaube, Eric S. Saltzman, Michael J. Behrenfeld, and Richard H. Moore
Atmos. Chem. Phys., 22, 2795–2815, https://doi.org/10.5194/acp-22-2795-2022, https://doi.org/10.5194/acp-22-2795-2022, 2022
Short summary
Short summary
Atmospheric particle concentrations impact clouds, which strongly impact the amount of sunlight reflected back into space and the overall climate. Measurements of particles over the ocean are rare and expensive to collect, so models are necessary to fill in the gaps by simulating both particle and clouds. However, some measurements are needed to test the accuracy of the models. Here, we measure changes in particles in different weather conditions, which are ideal for comparison with models.
Amie Dobracki, Paquita Zuidema, Steve Howell, Pablo Saide, Steffen Freitag, Allison C. Aiken, Sharon P. Burton, Arthur J. Sedlacek III, Jens Redemann, and Robert Wood
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2021-1081, https://doi.org/10.5194/acp-2021-1081, 2022
Preprint withdrawn
Short summary
Short summary
The global maximum of shortwave-absorbing aerosol above cloud occurs above the southeast Atlantic, where the biomass-burning aerosol provides a distinct aerosol radiative warming of regional climate. The smoke aerosols are unusually highly absorbing of sunlight. This study seeks to understand the cause. We conclude the aerosol is already strongly absorbing at the fire emission source, but that chemical aging, through encouraging a net loss of organic aerosol, also contributes.
Madison L. Ghiz, Ryan C. Scott, Andrew M. Vogelmann, Jan T. M. Lenaerts, Matthew Lazzara, and Dan Lubin
The Cryosphere, 15, 3459–3494, https://doi.org/10.5194/tc-15-3459-2021, https://doi.org/10.5194/tc-15-3459-2021, 2021
Short summary
Short summary
We investigate how melt occurs over the vulnerable ice shelves of West Antarctica and determine that the three primary mechanisms can be evaluated using archived numerical weather prediction model data and satellite imagery. We find examples of each mechanism: thermal blanketing by a warm atmosphere, radiative heating by thin clouds, and downslope winds. Our results signify the potential to make a multi-decadal assessment of atmospheric stress on West Antarctic ice shelves in a warming climate.
Yang Wang, Guangjie Zheng, Michael P. Jensen, Daniel A. Knopf, Alexander Laskin, Alyssa A. Matthews, David Mechem, Fan Mei, Ryan Moffet, Arthur J. Sedlacek, John E. Shilling, Stephen Springston, Amy Sullivan, Jason Tomlinson, Daniel Veghte, Rodney Weber, Robert Wood, Maria A. Zawadowicz, and Jian Wang
Atmos. Chem. Phys., 21, 11079–11098, https://doi.org/10.5194/acp-21-11079-2021, https://doi.org/10.5194/acp-21-11079-2021, 2021
Short summary
Short summary
This paper reports the vertical profiles of trace gas and aerosol properties over the eastern North Atlantic, a region of persistent but diverse subtropical marine boundary layer (MBL) clouds. We examined the key processes that drive the cloud condensation nuclei (CCN) population and how it varies with season and synoptic conditions. This study helps improve the model representation of the aerosol processes in the remote MBL, reducing the simulated aerosol indirect effects.
Maria A. Zawadowicz, Kaitlyn Suski, Jiumeng Liu, Mikhail Pekour, Jerome Fast, Fan Mei, Arthur J. Sedlacek, Stephen Springston, Yang Wang, Rahul A. Zaveri, Robert Wood, Jian Wang, and John E. Shilling
Atmos. Chem. Phys., 21, 7983–8002, https://doi.org/10.5194/acp-21-7983-2021, https://doi.org/10.5194/acp-21-7983-2021, 2021
Short summary
Short summary
This paper describes the results of a recent field campaign in the eastern North Atlantic, where two mass spectrometers were deployed aboard a research aircraft to measure the chemistry of aerosols and trace gases. Very clean conditions were found, dominated by local sulfate-rich acidic aerosol and very aged organics. Evidence of
long-range transport of aerosols from the continents was also identified.
Anna L. Hodshire, Emily Ramnarine, Ali Akherati, Matthew L. Alvarado, Delphine K. Farmer, Shantanu H. Jathar, Sonia M. Kreidenweis, Chantelle R. Lonsdale, Timothy B. Onasch, Stephen R. Springston, Jian Wang, Yang Wang, Lawrence I. Kleinman, Arthur J. Sedlacek III, and Jeffrey R. Pierce
Atmos. Chem. Phys., 21, 6839–6855, https://doi.org/10.5194/acp-21-6839-2021, https://doi.org/10.5194/acp-21-6839-2021, 2021
Short summary
Short summary
Biomass burning emits particles and vapors that can impact both health and climate. Here, we investigate the role of dilution in the evolution of aerosol size and composition in observed US wildfire smoke plumes. Centers of plumes dilute more slowly than edges. We see differences in concentrations and composition between the centers and edges both in the first measurement and in subsequent measurements. Our findings support the hypothesis that plume dilution influences smoke aging.
Franziska Köllner, Johannes Schneider, Megan D. Willis, Hannes Schulz, Daniel Kunkel, Heiko Bozem, Peter Hoor, Thomas Klimach, Frank Helleis, Julia Burkart, W. Richard Leaitch, Amir A. Aliabadi, Jonathan P. D. Abbatt, Andreas B. Herber, and Stephan Borrmann
Atmos. Chem. Phys., 21, 6509–6539, https://doi.org/10.5194/acp-21-6509-2021, https://doi.org/10.5194/acp-21-6509-2021, 2021
Short summary
Short summary
We present in situ observations of vertically resolved particle chemical composition in the summertime Arctic lower troposphere. Our analysis demonstrates the strong vertical contrast between particle properties within the boundary layer and aloft. Emissions from vegetation fires and anthropogenic sources in northern Canada, Europe, and East Asia influenced particle composition in the free troposphere. Organics detected in Arctic aerosol particles can partly be identified as dicarboxylic acids.
Kevin J. Sanchez, Gregory C. Roberts, Georges Saliba, Lynn M. Russell, Cynthia Twohy, J. Michael Reeves, Ruhi S. Humphries, Melita D. Keywood, Jason P. Ward, and Ian M. McRobert
Atmos. Chem. Phys., 21, 3427–3446, https://doi.org/10.5194/acp-21-3427-2021, https://doi.org/10.5194/acp-21-3427-2021, 2021
Short summary
Short summary
Measurements of particles and their properties were made from aircraft over the Southern Ocean. Aerosol transported from the Antarctic coast is shown to greatly enhance particle concentrations over the Southern Ocean. The occurrence of precipitation was shown to be associated with the lowest particle concentrations over the Southern Ocean. These particles are important due to their ability to enhance cloud droplet concentrations, resulting in more sunlight being reflected by the clouds.
Betty Croft, Randall V. Martin, Richard H. Moore, Luke D. Ziemba, Ewan C. Crosbie, Hongyu Liu, Lynn M. Russell, Georges Saliba, Armin Wisthaler, Markus Müller, Arne Schiller, Martí Galí, Rachel Y.-W. Chang, Erin E. McDuffie, Kelsey R. Bilsback, and Jeffrey R. Pierce
Atmos. Chem. Phys., 21, 1889–1916, https://doi.org/10.5194/acp-21-1889-2021, https://doi.org/10.5194/acp-21-1889-2021, 2021
Short summary
Short summary
North Atlantic Aerosols and Marine Ecosystems Study measurements combined with GEOS-Chem-TOMAS modeling suggest that several not-well-understood key factors control northwest Atlantic aerosol number and size. These synergetic and climate-relevant factors include particle formation near and above the marine boundary layer top, particle growth by marine secondary organic aerosol on descent, particle formation/growth related to dimethyl sulfide, sea spray aerosol, and ship emissions.
Kevin J. Sanchez, Bo Zhang, Hongyu Liu, Georges Saliba, Chia-Li Chen, Savannah L. Lewis, Lynn M. Russell, Michael A. Shook, Ewan C. Crosbie, Luke D. Ziemba, Matthew D. Brown, Taylor J. Shingler, Claire E. Robinson, Elizabeth B. Wiggins, Kenneth L. Thornhill, Edward L. Winstead, Carolyn Jordan, Patricia K. Quinn, Timothy S. Bates, Jack Porter, Thomas G. Bell, Eric S. Saltzman, Michael J. Behrenfeld, and Richard H. Moore
Atmos. Chem. Phys., 21, 831–851, https://doi.org/10.5194/acp-21-831-2021, https://doi.org/10.5194/acp-21-831-2021, 2021
Short summary
Short summary
Models describing atmospheric airflow were combined with satellite measurements representative of marine phytoplankton and other meteorological variables. These combined variables were compared to measured aerosol to identify upwind influences on aerosol concentrations. Results indicate that phytoplankton production rates upwind impact the aerosol mass. Also, results suggest that the condensation of mass onto short-lived large sea spray particles may be a significant sink of aerosol mass.
Michael J. Lawler, Savannah L. Lewis, Lynn M. Russell, Patricia K. Quinn, Timothy S. Bates, Derek J. Coffman, Lucia M. Upchurch, and Eric S. Saltzman
Atmos. Chem. Phys., 20, 16007–16022, https://doi.org/10.5194/acp-20-16007-2020, https://doi.org/10.5194/acp-20-16007-2020, 2020
Short summary
Short summary
This work describes new measurements of aerosol (particles) composition over the North Atlantic Ocean. It provides concentrations of polysaccharide material likely made from organisms in the surface ocean and improves our understanding of the relative importance of such fresh biogenic material compared to more recalcitrant organic carbon in forming marine organic aerosol. We aim ultimately to understand the role that ocean biology plays in cloud formation in marine regions.
Lawrence I. Kleinman, Arthur J. Sedlacek III, Kouji Adachi, Peter R. Buseck, Sonya Collier, Manvendra K. Dubey, Anna L. Hodshire, Ernie Lewis, Timothy B. Onasch, Jeffery R. Pierce, John Shilling, Stephen R. Springston, Jian Wang, Qi Zhang, Shan Zhou, and Robert J. Yokelson
Atmos. Chem. Phys., 20, 13319–13341, https://doi.org/10.5194/acp-20-13319-2020, https://doi.org/10.5194/acp-20-13319-2020, 2020
Short summary
Short summary
Aerosols from wildfires affect the Earth's temperature by absorbing light or reflecting it back into space. This study investigates time-dependent chemical, microphysical, and optical properties of aerosols generated by wildfires in the Pacific Northwest, USA. Wildfire smoke plumes were traversed by an instrumented aircraft at locations near the fire and up to 3.5 h travel time downwind. Although there was no net aerosol production, aerosol particles grew and became more efficient scatters.
Guangjie Zheng, Chongai Kuang, Janek Uin, Thomas Watson, and Jian Wang
Atmos. Chem. Phys., 20, 12515–12525, https://doi.org/10.5194/acp-20-12515-2020, https://doi.org/10.5194/acp-20-12515-2020, 2020
Short summary
Short summary
Condensational growth of Aitken-mode particles is a major source of cloud condensation nuclei in the remote marine boundary layer. It has been long thought that over remote oceans, condensation growth is dominated by sulfate that derives from ocean-emitted dimethyl sulfide. In this study, we present the first long-term observational evidence that, contrary to conventional thinking, organics play an even more important role than sulfate in particle growth over remote oceans throughout the year.
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
Short summary
Short summary
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.
Luke T. Cravigan, Marc D. Mallet, Petri Vaattovaara, Mike J. Harvey, Cliff S. Law, Robin L. Modini, Lynn M. Russell, Ed Stelcer, David D. Cohen, Greg Olsen, Karl Safi, Timothy J. Burrell, and Zoran Ristovski
Atmos. Chem. Phys., 20, 7955–7977, https://doi.org/10.5194/acp-20-7955-2020, https://doi.org/10.5194/acp-20-7955-2020, 2020
Short summary
Short summary
Aerosol–cloud interactions in remote marine environments are poorly represented in atmospheric modelling, particularly over the Southern Hemisphere. This work reports in situ chamber observations of sea spray aerosol composition and water uptake during the Surface Ocean Aerosol Production (SOAP) voyage. Observations were compared with currently applied models for sea spray organic enrichment. The sea spray hygroscopicity was persistently high, even at high organic fractions.
Francesca Gallo, Janek Uin, Stephen Springston, Jian Wang, Guangjie Zheng, Chongai Kuang, Robert Wood, Eduardo B. Azevedo, Allison McComiskey, Fan Mei, Adam Theisen, Jenni Kyrouac, and Allison C. Aiken
Atmos. Chem. Phys., 20, 7553–7573, https://doi.org/10.5194/acp-20-7553-2020, https://doi.org/10.5194/acp-20-7553-2020, 2020
Short summary
Short summary
Continuous high-time-resolution ambient data can include periods when aerosol properties do not represent regional aerosol processes due to high-concentration local events. We develop a novel aerosol mask at the U.S. Department of Energy’s Atmospheric Radiation Measurement (ARM) facility in the eastern North Atlantic (ENA). We use two ground sites to validate the mask, include a comparison with aircraft overflights, and provide guidance to increase data quality at ENA and other locations.
Fan Mei, Jian Wang, Jennifer M. Comstock, Ralf Weigel, Martina Krämer, Christoph Mahnke, John E. Shilling, Johannes Schneider, Christiane Schulz, Charles N. Long, Manfred Wendisch, Luiz A. T. Machado, Beat Schmid, Trismono Krisna, Mikhail Pekour, John Hubbe, Andreas Giez, Bernadett Weinzierl, Martin Zoeger, Mira L. Pöhlker, Hans Schlager, Micael A. Cecchini, Meinrat O. Andreae, Scot T. Martin, Suzane S. de Sá, Jiwen Fan, Jason Tomlinson, Stephen Springston, Ulrich Pöschl, Paulo Artaxo, Christopher Pöhlker, Thomas Klimach, Andreas Minikin, Armin Afchine, and Stephan Borrmann
Atmos. Meas. Tech., 13, 661–684, https://doi.org/10.5194/amt-13-661-2020, https://doi.org/10.5194/amt-13-661-2020, 2020
Short summary
Short summary
In 2014, the US DOE G1 aircraft and the German HALO aircraft overflew the Amazon basin to study how aerosols influence cloud cycles under a clean condition and around a tropical megacity. This paper describes how to meaningfully compare similar measurements from two research aircraft and identify the potential measurement issue. We also discuss the uncertainty range for each measurement for further usage in model evaluation and satellite data validation.
Joelle Dionne, Knut von Salzen, Jason Cole, Rashed Mahmood, W. Richard Leaitch, Glen Lesins, Ian Folkins, and Rachel Y.-W. Chang
Atmos. Chem. Phys., 20, 29–43, https://doi.org/10.5194/acp-20-29-2020, https://doi.org/10.5194/acp-20-29-2020, 2020
Short summary
Short summary
Low clouds persist in the summer Arctic, with important consequences for the radiation budget. We found that the ability of precipitation parameterizations to reproduce observed cloud properties was more variable than their ability to represent radiative effects. Our results show that cloud properties and their parameterizations affect the radiative effects of clouds.
Heiko Bozem, Peter Hoor, Daniel Kunkel, Franziska Köllner, Johannes Schneider, Andreas Herber, Hannes Schulz, W. Richard Leaitch, Amir A. Aliabadi, Megan D. Willis, Julia Burkart, and Jonathan P. D. Abbatt
Atmos. Chem. Phys., 19, 15049–15071, https://doi.org/10.5194/acp-19-15049-2019, https://doi.org/10.5194/acp-19-15049-2019, 2019
Short summary
Short summary
We present airborne trace gas measurements in the European and Canadian Arctic for July 2014 and April 2015. Based on CO and CO2 in situ data as well as 10 d kinematic back trajectories, we characterize the prevailing transport regimes and derive a tracer-based diagnostic for the determination of the polar dome boundary. Using the tracer-derived boundary, an analysis of the recent transport history of air masses within the polar dome reveals significant differences between spring and summer.
Roya Ghahreman, Wanmin Gong, Martí Galí, Ann-Lise Norman, Stephen R. Beagley, Ayodeji Akingunola, Qiong Zheng, Alexandru Lupu, Martine Lizotte, Maurice Levasseur, and W. Richard Leaitch
Atmos. Chem. Phys., 19, 14455–14476, https://doi.org/10.5194/acp-19-14455-2019, https://doi.org/10.5194/acp-19-14455-2019, 2019
Short summary
Short summary
Atmospheric DMS(g) is a climatically important compound and the main source of biogenic sulfate in the Arctic. Its abundance in the Arctic increases during summer due to greater ice-free sea surface and higher biological activity. In this study, we implemented DMS(g) in a regional air quality forecast model configured for the Arctic. The study showed a significant impact from DMS(g) on sulfate aerosols, particularly in the 50–100 nm size range, in the Arctic marine boundary layer during summer.
Keith M. Hines, David H. Bromwich, Sheng-Hung Wang, Israel Silber, Johannes Verlinde, and Dan Lubin
Atmos. Chem. Phys., 19, 12431–12454, https://doi.org/10.5194/acp-19-12431-2019, https://doi.org/10.5194/acp-19-12431-2019, 2019
Short summary
Short summary
We explore how well clouds are represented in numerical weather prediction over Antarctica, a very difficult environment for field programs where few studies have been conducted. Fortunately, a 2015–2017 field program for West Antarctica supplied observations. We achieve promising results with newer, more advanced cloud schemes. We need to understand the role of clouds and precipitation in the maintenance of the Antarctic ice mass to understand and predict sea level change over the 21st century.
Suzane S. de Sá, Luciana V. Rizzo, Brett B. Palm, Pedro Campuzano-Jost, Douglas A. Day, Lindsay D. Yee, Rebecca Wernis, Gabriel Isaacman-VanWertz, Joel Brito, Samara Carbone, Yingjun J. Liu, Arthur Sedlacek, Stephen Springston, Allen H. Goldstein, Henrique M. J. Barbosa, M. Lizabeth Alexander, Paulo Artaxo, Jose L. Jimenez, and Scot T. Martin
Atmos. Chem. Phys., 19, 7973–8001, https://doi.org/10.5194/acp-19-7973-2019, https://doi.org/10.5194/acp-19-7973-2019, 2019
Short summary
Short summary
This study investigates the impacts of urban and fire emissions on the concentration, composition, and optical properties of submicron particulate matter (PM1) in central Amazonia during the dry season. Biomass-burning and urban emissions appeared to contribute at least 80 % of brown carbon absorption while accounting for 30 % to 40 % of the organic PM1 mass concentration. Only a fraction of the 9-fold increase in mass concentration relative to the wet season was due to biomass burning.
Samantha Tremblay, Jean-Christophe Picard, Jill O. Bachelder, Erik Lutsch, Kimberly Strong, Pierre Fogal, W. Richard Leaitch, Sangeeta Sharma, Felicia Kolonjari, Christopher J. Cox, Rachel Y.-W. Chang, and Patrick L. Hayes
Atmos. Chem. Phys., 19, 5589–5604, https://doi.org/10.5194/acp-19-5589-2019, https://doi.org/10.5194/acp-19-5589-2019, 2019
Short summary
Short summary
Atmospheric aerosols, tiny airborne particles, have an important impact on climate. However, a lack of understanding of the chemistry of aerosols is one of the largest contributors to uncertainty in predictions of climate change. Measurements of aerosols were carried out in the Arctic at Eureka Station, Canada, to better understand what role aerosols play in this fragile environment. It is found that organic aerosols, possibly originating from marine emissions, are ubiquitous during summertime.
Meng Si, Erin Evoy, Jingwei Yun, Yu Xi, Sarah J. Hanna, Alina Chivulescu, Kevin Rawlings, Daniel Veber, Andrew Platt, Daniel Kunkel, Peter Hoor, Sangeeta Sharma, W. Richard Leaitch, and Allan K. Bertram
Atmos. Chem. Phys., 19, 3007–3024, https://doi.org/10.5194/acp-19-3007-2019, https://doi.org/10.5194/acp-19-3007-2019, 2019
Short summary
Short summary
We investigated the importance of mineral dust, sea spray aerosol, and anthropogenic aerosol to the ice-nucleating particle (INP) population in the Canadian Arctic during spring 2016. The results suggest that mineral dust transported from the Gobi Desert was a major source of the INP population studied, and that sea spray aerosol decreased the ice-nucleating ability of mineral dust. The results should be useful for testing and improving models used to predict INPs and climate in the Arctic.
Betty Croft, Randall V. Martin, W. Richard Leaitch, Julia Burkart, Rachel Y.-W. Chang, Douglas B. Collins, Patrick L. Hayes, Anna L. Hodshire, Lin Huang, John K. Kodros, Alexander Moravek, Emma L. Mungall, Jennifer G. Murphy, Sangeeta Sharma, Samantha Tremblay, Gregory R. Wentworth, Megan D. Willis, Jonathan P. D. Abbatt, and Jeffrey R. Pierce
Atmos. Chem. Phys., 19, 2787–2812, https://doi.org/10.5194/acp-19-2787-2019, https://doi.org/10.5194/acp-19-2787-2019, 2019
Short summary
Short summary
Summertime Arctic atmospheric aerosols are strongly controlled by processes related to natural regional sources. We use a chemical transport model with size-resolved aerosol microphysics to interpret measurements made during summertime 2016 in the Canadian Arctic Archipelago. Our results explore the processes that control summertime aerosol size distributions and support a climate-relevant role for Arctic marine secondary organic aerosol formed from precursor vapors with Arctic marine sources.
Jonathan P. D. Abbatt, W. Richard Leaitch, Amir A. Aliabadi, Allan K. Bertram, Jean-Pierre Blanchet, Aude Boivin-Rioux, Heiko Bozem, Julia Burkart, Rachel Y. W. Chang, Joannie Charette, Jai P. Chaubey, Robert J. Christensen, Ana Cirisan, Douglas B. Collins, Betty Croft, Joelle Dionne, Greg J. Evans, Christopher G. Fletcher, Martí Galí, Roya Ghahreman, Eric Girard, Wanmin Gong, Michel Gosselin, Margaux Gourdal, Sarah J. Hanna, Hakase Hayashida, Andreas B. Herber, Sareh Hesaraki, Peter Hoor, Lin Huang, Rachel Hussherr, Victoria E. Irish, Setigui A. Keita, John K. Kodros, Franziska Köllner, Felicia Kolonjari, Daniel Kunkel, Luis A. Ladino, Kathy Law, Maurice Levasseur, Quentin Libois, John Liggio, Martine Lizotte, Katrina M. Macdonald, Rashed Mahmood, Randall V. Martin, Ryan H. Mason, Lisa A. Miller, Alexander Moravek, Eric Mortenson, Emma L. Mungall, Jennifer G. Murphy, Maryam Namazi, Ann-Lise Norman, Norman T. O'Neill, Jeffrey R. Pierce, Lynn M. Russell, Johannes Schneider, Hannes Schulz, Sangeeta Sharma, Meng Si, Ralf M. Staebler, Nadja S. Steiner, Jennie L. Thomas, Knut von Salzen, Jeremy J. B. Wentzell, Megan D. Willis, Gregory R. Wentworth, Jun-Wei Xu, and Jacqueline D. Yakobi-Hancock
Atmos. Chem. Phys., 19, 2527–2560, https://doi.org/10.5194/acp-19-2527-2019, https://doi.org/10.5194/acp-19-2527-2019, 2019
Short summary
Short summary
The Arctic is experiencing considerable environmental change with climate warming, illustrated by the dramatic decrease in sea-ice extent. It is important to understand both the natural and perturbed Arctic systems to gain a better understanding of how they will change in the future. This paper summarizes new insights into the relationships between Arctic aerosol particles and climate, as learned over the past five or so years by a large Canadian research consortium, NETCARE.
Hannes Schulz, Marco Zanatta, Heiko Bozem, W. Richard Leaitch, Andreas B. Herber, Julia Burkart, Megan D. Willis, Daniel Kunkel, Peter M. Hoor, Jonathan P. D. Abbatt, and Rüdiger Gerdes
Atmos. Chem. Phys., 19, 2361–2384, https://doi.org/10.5194/acp-19-2361-2019, https://doi.org/10.5194/acp-19-2361-2019, 2019
Short summary
Short summary
Aircraft vertical profiles of black carbon (BC) aerosol from the High Canadian Arctic have shown systematic variability in different levels of the cold, stably stratified polar dome. During spring and summer, efficiencies of BC supply by transport (often from gas flaring and wildfire-affected regions) were different in the lower dome than at higher levels, as apparent from changes in mean particle size and mixing ratios with CO. Summer BC concentrations were a factor of 10 lower than in spring.
Victoria E. Irish, Sarah J. Hanna, Megan D. Willis, Swarup China, Jennie L. Thomas, Jeremy J. B. Wentzell, Ana Cirisan, Meng Si, W. Richard Leaitch, Jennifer G. Murphy, Jonathan P. D. Abbatt, Alexander Laskin, Eric Girard, and Allan K. Bertram
Atmos. Chem. Phys., 19, 1027–1039, https://doi.org/10.5194/acp-19-1027-2019, https://doi.org/10.5194/acp-19-1027-2019, 2019
Short summary
Short summary
Ice nucleating particles (INPs) are atmospheric particles that catalyse the formation of ice crystals in clouds. INPs influence the Earth's radiative balance and hydrological cycle. In this study we measured the concentrations of INPs in the Canadian Arctic marine boundary layer. Average INP concentrations fell within the range measured in other marine boundary layer locations. We also found that mineral dust is a more important contributor to the INP population than sea spray aerosol.
Megan D. Willis, Heiko Bozem, Daniel Kunkel, Alex K. Y. Lee, Hannes Schulz, Julia Burkart, Amir A. Aliabadi, Andreas B. Herber, W. Richard Leaitch, and Jonathan P. D. Abbatt
Atmos. Chem. Phys., 19, 57–76, https://doi.org/10.5194/acp-19-57-2019, https://doi.org/10.5194/acp-19-57-2019, 2019
Short summary
Short summary
The vertical distribution of Arctic aerosol is an important driver of its climate impacts. We present vertically resolved measurements of aerosol composition and properties made in the High Arctic during spring on an aircraft platform. We explore how aerosol properties are related to transport history and show evidence of vertical trends in aerosol sources, transport mechanisms and composition. These results will help us to better understand aerosol–climate interactions in the Arctic.
Johannes Mülmenstädt, Odran Sourdeval, David S. Henderson, Tristan S. L'Ecuyer, Claudia Unglaub, Leonore Jungandreas, Christoph Böhm, Lynn M. Russell, and Johannes Quaas
Earth Syst. Sci. Data, 10, 2279–2293, https://doi.org/10.5194/essd-10-2279-2018, https://doi.org/10.5194/essd-10-2279-2018, 2018
Short summary
Short summary
One of the key pieces of information about a cloud is how high its base is. Unlike cloud top, cloud base is hard to observe from a satellite perspective – the cloud blocks the view. But without using satellites, it is difficult to compile global datasets. Here we describe how we worked around the limitations of a cloud-detecting laser satellite to observe global cloud base heights. This dataset will expand our knowledge of the cloudy atmosphere and its interaction with the planetary surface.
Guangjie Zheng, Yang Wang, Allison C. Aiken, Francesca Gallo, Michael P. Jensen, Pavlos Kollias, Chongai Kuang, Edward Luke, Stephen Springston, Janek Uin, Robert Wood, and Jian Wang
Atmos. Chem. Phys., 18, 17615–17635, https://doi.org/10.5194/acp-18-17615-2018, https://doi.org/10.5194/acp-18-17615-2018, 2018
Short summary
Short summary
Here, we elucidate the key processes that drive marine boundary layer (MBL) aerosol size distribution in the eastern North Atlantic (ENA) using long-term measurements. The governing equations of particle concentration are established for different modes. Particles entrained from the free troposphere represent the major source of MBL cloud condensation nuclei (CCN), contributing both directly to CCN population and indirectly by supplying Aitken-mode particles that grow to CCN in the MBL.
Tuomo Nieminen, Veli-Matti Kerminen, Tuukka Petäjä, Pasi P. Aalto, Mikhail Arshinov, Eija Asmi, Urs Baltensperger, David C. S. Beddows, Johan Paul Beukes, Don Collins, Aijun Ding, Roy M. Harrison, Bas Henzing, Rakesh Hooda, Min Hu, Urmas Hõrrak, Niku Kivekäs, Kaupo Komsaare, Radovan Krejci, Adam Kristensson, Lauri Laakso, Ari Laaksonen, W. Richard Leaitch, Heikki Lihavainen, Nikolaos Mihalopoulos, Zoltán Németh, Wei Nie, Colin O'Dowd, Imre Salma, Karine Sellegri, Birgitta Svenningsson, Erik Swietlicki, Peter Tunved, Vidmantas Ulevicius, Ville Vakkari, Marko Vana, Alfred Wiedensohler, Zhijun Wu, Annele Virtanen, and Markku Kulmala
Atmos. Chem. Phys., 18, 14737–14756, https://doi.org/10.5194/acp-18-14737-2018, https://doi.org/10.5194/acp-18-14737-2018, 2018
Short summary
Short summary
Atmospheric aerosols have diverse effects on air quality, human health, and global climate. One important source of aerosols is their formation via nucleation and growth in the atmosphere. We have analyzed long-term observations of regional new particle formation events around the globe and provide a comprehensive view on the characteristics of this phenomenon in diverse environments. The results are useful in developing more realistic representation of atmospheric aerosols in global models.
Daniela Wimmer, Stephany Buenrostro Mazon, Hanna Elina Manninen, Juha Kangasluoma, Alessandro Franchin, Tuomo Nieminen, John Backman, Jian Wang, Chongai Kuang, Radovan Krejci, Joel Brito, Fernando Goncalves Morais, Scot Turnbull Martin, Paulo Artaxo, Markku Kulmala, Veli-Matti Kerminen, and Tuukka Petäjä
Atmos. Chem. Phys., 18, 13245–13264, https://doi.org/10.5194/acp-18-13245-2018, https://doi.org/10.5194/acp-18-13245-2018, 2018
Short summary
Short summary
This work focuses on understanding the production of very small airborne particles in the undisturbed environment of the Amazon basin. Computer models have shown that up to 70 % of these tiny particles are responsible for cloud formation on a global scale. The processes behind the production of these very small particles have been studied intensely recently. Their appearance has been observed almost all over the world. We directly measure sub-3 nm aerosols for the first time in the Amazon basin.
John K. Kodros, Sarah J. Hanna, Allan K. Bertram, W. Richard Leaitch, Hannes Schulz, Andreas B. Herber, Marco Zanatta, Julia Burkart, Megan D. Willis, Jonathan P. D. Abbatt, and Jeffrey R. Pierce
Atmos. Chem. Phys., 18, 11345–11361, https://doi.org/10.5194/acp-18-11345-2018, https://doi.org/10.5194/acp-18-11345-2018, 2018
Short summary
Short summary
The mixing state of black carbon is one of the key uncertainties limiting the ability of models to estimate the direct radiative effect. In this work, we present aircraft measurements from the Canadian Arctic of coating thickness as a function of black carbon core diameter and black-carbon-containing particle number fractions. We use these measurements to inform estimates of the direct radiative effect in Arctic aerosol simulations.
Arthur J. Sedlacek III, Peter R. Buseck, Kouji Adachi, Timothy B. Onasch, Stephen R. Springston, and Lawrence Kleinman
Atmos. Chem. Phys., 18, 11289–11301, https://doi.org/10.5194/acp-18-11289-2018, https://doi.org/10.5194/acp-18-11289-2018, 2018
Short summary
Short summary
This paper presents the first direct atmospheric observations of the formation and evolution of tar balls (TBs) in forest fires collected during the Department of Energy’s Biomass Burning Observation Project (BBOP). We quantify, for the first time, the TB mass fraction in the BB plumes and show that this mass fraction increases from less than 1 % to 50 % within the first couple of hours of plume aging. Using Mie theory we find that TBs are consistent with being weak light absorbers.
John E. Shilling, Mikhail S. Pekour, Edward C. Fortner, Paulo Artaxo, Suzane de Sá, John M. Hubbe, Karla M. Longo, Luiz A. T. Machado, Scot T. Martin, Stephen R. Springston, Jason Tomlinson, and Jian Wang
Atmos. Chem. Phys., 18, 10773–10797, https://doi.org/10.5194/acp-18-10773-2018, https://doi.org/10.5194/acp-18-10773-2018, 2018
Short summary
Short summary
We report aircraft observations of the evolution of organic aerosol in the Manaus urban plume as it ages. We observe dynamic changes in the organic aerosol. The mean carbon oxidation state of the OA increases from −0.6 to −0.45. Hydrocarbon-like organic aerosol (HOA) mass is lost and is balanced out by formation of oxygenated organic aerosol (OOA). Because HOA loss is balanced by OOA formation, we observe little change in the net Δorg / ΔCO values with aging.
Katrina M. Macdonald, Sangeeta Sharma, Desiree Toom, Alina Chivulescu, Andrew Platt, Mike Elsasser, Lin Huang, Richard Leaitch, Nathan Chellman, Joseph R. McConnell, Heiko Bozem, Daniel Kunkel, Ying Duan Lei, Cheol-Heon Jeong, Jonathan P. D. Abbatt, and Greg J. Evans
Atmos. Chem. Phys., 18, 3485–3503, https://doi.org/10.5194/acp-18-3485-2018, https://doi.org/10.5194/acp-18-3485-2018, 2018
Short summary
Short summary
The sources of key contaminants in Arctic snow may be an important factor in understanding the rapid climate changes observed in the Arctic. Fresh snow samples collected frequently through the winter season were analyzed for major constituents. Temporally refined source apportionment via positive matrix factorization in conjunction with FLEXPART suggested potential source characteristics and locations. The identity of these sources and their relative contribution to key analytes is discussed.
W. Richard Leaitch, Lynn M. Russell, Jun Liu, Felicia Kolonjari, Desiree Toom, Lin Huang, Sangeeta Sharma, Alina Chivulescu, Dan Veber, and Wendy Zhang
Atmos. Chem. Phys., 18, 3269–3287, https://doi.org/10.5194/acp-18-3269-2018, https://doi.org/10.5194/acp-18-3269-2018, 2018
Short summary
Short summary
Over 2 years of atmospheric aerosol organic functional group and microphysics measurements at the world's northernmost land observatory offer a unique high-latitude dataset. Lower organic mass (OM) concentrations and higher OM fractions accompany smaller particles during summer, with opposite results during winter to spring. Seasonally, the OM oxidation level is highest in winter, associated with primary marine alcohol groups. In summer, secondary processes dominate the marine influence on OM.
Brett B. Palm, Suzane S. de Sá, Douglas A. Day, Pedro Campuzano-Jost, Weiwei Hu, Roger Seco, Steven J. Sjostedt, Jeong-Hoo Park, Alex B. Guenther, Saewung Kim, Joel Brito, Florian Wurm, Paulo Artaxo, Ryan Thalman, Jian Wang, Lindsay D. Yee, Rebecca Wernis, Gabriel Isaacman-VanWertz, Allen H. Goldstein, Yingjun Liu, Stephen R. Springston, Rodrigo Souza, Matt K. Newburn, M. Lizabeth Alexander, Scot T. Martin, and Jose L. Jimenez
Atmos. Chem. Phys., 18, 467–493, https://doi.org/10.5194/acp-18-467-2018, https://doi.org/10.5194/acp-18-467-2018, 2018
Short summary
Short summary
Ambient air was oxidized by OH or O3 in an oxidation flow reactor during both wet and dry seasons in the GoAmazon2014/5 campaign to study secondary organic aerosol (SOA) formation. We investigated how much biogenic, urban, and biomass burning sources contributed to the ambient concentrations of SOA precursor gases and how their contributions changed diurnally and seasonally. SOA yields and hygroscopicity of organic aerosol in the oxidation flow reactor were also studied.
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
Short summary
Short summary
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.
Alex K. Y. Lee, Chia-Li Chen, Jun Liu, Derek J. Price, Raghu Betha, Lynn M. Russell, Xiaolu Zhang, and Christopher D. Cappa
Atmos. Chem. Phys., 17, 15055–15067, https://doi.org/10.5194/acp-17-15055-2017, https://doi.org/10.5194/acp-17-15055-2017, 2017
Short summary
Short summary
Understanding the mixing state of ambient black carbon (BC) and the chemical characteristics of its associated coatings is important to evaluate BC fate and environmental impacts. This study reports fresh secondary organic aerosol (SOA) formation near traffic emissions during daytime. Our observations suggest that BC was unlikely the major condensation sink of SOA, and a portion of SOA condensed on BC surface was chemically different from other SOA particles that were externally mixed with BC.
Franziska Köllner, Johannes Schneider, Megan D. Willis, Thomas Klimach, Frank Helleis, Heiko Bozem, Daniel Kunkel, Peter Hoor, Julia Burkart, W. Richard Leaitch, Amir A. Aliabadi, Jonathan P. D. Abbatt, Andreas B. Herber, and Stephan Borrmann
Atmos. Chem. Phys., 17, 13747–13766, https://doi.org/10.5194/acp-17-13747-2017, https://doi.org/10.5194/acp-17-13747-2017, 2017
Short summary
Short summary
We conducted aircraft-based single particle chemical composition measurements in the Canadian high Arctic during summer. Our results provide evidence for a marine-biogenic influence on secondary formation of particulate trimethylamine in the Arctic boundary layer. Understanding emission sources and further processes controlling aerosol number concentration and chemical composition in the pristine Arctic summer is crucial for modeling future climate in the area.
Ryan Thalman, Suzane S. de Sá, Brett B. Palm, Henrique M. J. Barbosa, Mira L. Pöhlker, M. Lizabeth Alexander, Joel Brito, Samara Carbone, Paulo Castillo, Douglas A. Day, Chongai Kuang, Antonio Manzi, Nga Lee Ng, Arthur J. Sedlacek III, Rodrigo Souza, Stephen Springston, Thomas Watson, Christopher Pöhlker, Ulrich Pöschl, Meinrat O. Andreae, Paulo Artaxo, Jose L. Jimenez, Scot T. Martin, and Jian Wang
Atmos. Chem. Phys., 17, 11779–11801, https://doi.org/10.5194/acp-17-11779-2017, https://doi.org/10.5194/acp-17-11779-2017, 2017
Short summary
Short summary
Particle hygroscopicity, mixing state, and the hygroscopicity of organic components were characterized in central Amazonia for 1 year; their seasonal and diel variations were driven by a combination of primary emissions, photochemical oxidation, and boundary layer development. The relationship between the hygroscopicity of organic components and their oxidation level was examined, and the results help to reconcile the differences among the relationships observed in previous studies.
Benjamin N. Murphy, Matthew C. Woody, Jose L. Jimenez, Ann Marie G. Carlton, Patrick L. Hayes, Shang Liu, Nga L. Ng, Lynn M. Russell, Ari Setyan, Lu Xu, Jeff Young, Rahul A. Zaveri, Qi Zhang, and Havala O. T. Pye
Atmos. Chem. Phys., 17, 11107–11133, https://doi.org/10.5194/acp-17-11107-2017, https://doi.org/10.5194/acp-17-11107-2017, 2017
Short summary
Short summary
We incorporate recent findings about the behavior of organic pollutants in urban airsheds into the Community Multiscale Air Quality (CMAQ) model to refine predictions of organic particulate pollution in the United States. The new techniques, which account for the volatility and ongoing chemistry of airborne organic compounds, substantially reduce biases, particularly in the winter time and near emission sources.
Kevin J. Sanchez, Gregory C. Roberts, Radiance Calmer, Keri Nicoll, Eyal Hashimshoni, Daniel Rosenfeld, Jurgita Ovadnevaite, Jana Preissler, Darius Ceburnis, Colin O'Dowd, and Lynn M. Russell
Atmos. Chem. Phys., 17, 9797–9814, https://doi.org/10.5194/acp-17-9797-2017, https://doi.org/10.5194/acp-17-9797-2017, 2017
Short summary
Short summary
Unmanned aerial vehicles are equipped with meteorological sensors to measure cloud properties. The measurements are used to calculate the amount of solar radiation reflected by the clouds and compared to simulation results. The uncertainties related to radiative forcing in the simulations are from the lack of mixing in the boundary layer and mixing of dry air into the cloud top. Conservative variables are used to calculate the amount of air mixed into cloud top to minimize these uncertainties.
Roya Ghahreman, Ann-Lise Norman, Betty Croft, Randall V. Martin, Jeffrey R. Pierce, Julia Burkart, Ofelia Rempillo, Heiko Bozem, Daniel Kunkel, Jennie L. Thomas, Amir A. Aliabadi, Gregory R. Wentworth, Maurice Levasseur, Ralf M. Staebler, Sangeeta Sharma, and W. Richard Leaitch
Atmos. Chem. Phys., 17, 8757–8770, https://doi.org/10.5194/acp-17-8757-2017, https://doi.org/10.5194/acp-17-8757-2017, 2017
Short summary
Short summary
We present spring and summertime vertical profile measurements of Arctic dimethyl sulfide (DMS), together with model simulations to consider what these profiles indicate about DMS sources and lifetimes in the Arctic. Our results highlight the role of local open water as the source of DMS(g) during July 2014 and the influence of long-range transport of DMS(g) from further afield in the Arctic during April 2015.
Suzane S. de Sá, Brett B. Palm, Pedro Campuzano-Jost, Douglas A. Day, Matthew K. Newburn, Weiwei Hu, Gabriel Isaacman-VanWertz, Lindsay D. Yee, Ryan Thalman, Joel Brito, Samara Carbone, Paulo Artaxo, Allen H. Goldstein, Antonio O. Manzi, Rodrigo A. F. Souza, Fan Mei, John E. Shilling, Stephen R. Springston, Jian Wang, Jason D. Surratt, M. Lizabeth Alexander, Jose L. Jimenez, and Scot T. Martin
Atmos. Chem. Phys., 17, 6611–6629, https://doi.org/10.5194/acp-17-6611-2017, https://doi.org/10.5194/acp-17-6611-2017, 2017
Julia Burkart, Megan D. Willis, Heiko Bozem, Jennie L. Thomas, Kathy Law, Peter Hoor, Amir A. Aliabadi, Franziska Köllner, Johannes Schneider, Andreas Herber, Jonathan P. D. Abbatt, and W. Richard Leaitch
Atmos. Chem. Phys., 17, 5515–5535, https://doi.org/10.5194/acp-17-5515-2017, https://doi.org/10.5194/acp-17-5515-2017, 2017
Short summary
Short summary
Our aircraft study for the first time systematically investigates aerosol size distributions, including ultrafine particles (5–20 nm in diameter), in the Arctic summertime atmosphere. We find that ultrafine particles occur very frequently in the boundary layer and not aloft, suggesting a surface source of these particles. Understanding aerosol properties and sources is crucial to predict climate and especially important in the Arctic as this region responds extremely fast to climate change.
Andrew D. Teakles, Rita So, Bruce Ainslie, Robert Nissen, Corinne Schiller, Roxanne Vingarzan, Ian McKendry, Anne Marie Macdonald, Daniel A. Jaffe, Allan K. Bertram, Kevin B. Strawbridge, W. Richard Leaitch, Sarah Hanna, Desiree Toom, Jonathan Baik, and Lin Huang
Atmos. Chem. Phys., 17, 2593–2611, https://doi.org/10.5194/acp-17-2593-2017, https://doi.org/10.5194/acp-17-2593-2017, 2017
Short summary
Short summary
We present a case study of an intense wildfire smoke plume from Siberia that affected the air quality across the Pacific Northwest on 6–10 July 2012. The transport, entrainment, and chemical composition of the plume are examined to characterize the event. Ambient O3 and PM2.5 from surface monitoring is contrast to modelled baseline air quality estimates to show the overall contribution of the plume to exceedances in O3 and PM2.5 air quality standards and objectives that occurred.
Quentin Libois, Liviu Ivanescu, Jean-Pierre Blanchet, Hannes Schulz, Heiko Bozem, W. Richard Leaitch, Julia Burkart, Jonathan P. D. Abbatt, Andreas B. Herber, Amir A. Aliabadi, and Éric Girard
Atmos. Chem. Phys., 16, 15689–15707, https://doi.org/10.5194/acp-16-15689-2016, https://doi.org/10.5194/acp-16-15689-2016, 2016
Short summary
Short summary
The first airborne measurements performed with the FIRR are presented. Vertical profiles of upwelling spectral radiance in the far-infrared are measured in the Arctic atmosphere for the first time. They show the impact of the temperature inversion on the radiative budget of the atmosphere, especially in the far-infrared. The presence of ice clouds also significantly alters the far-infrared budget, highlighting the critical interplay between water vapour and clouds in this very dry region.
Xuan Wang, Colette L. Heald, Arthur J. Sedlacek, Suzane S. de Sá, Scot T. Martin, M. Lizabeth Alexander, Thomas B. Watson, Allison C. Aiken, Stephen R. Springston, and Paulo Artaxo
Atmos. Chem. Phys., 16, 12733–12752, https://doi.org/10.5194/acp-16-12733-2016, https://doi.org/10.5194/acp-16-12733-2016, 2016
Short summary
Short summary
We describe a new approach to estimate the absorption of brown carbon (BrC) from multiple-wavelength absorption measurements. By applying this method to column and surface observations globally, we find that BrC contributes up to 40 % of the absorption measured at 440 nm. The analysis of two surface sites also suggests that BrC absorptivity decreases with photochemical aging in biomass burning plumes, but not in typical urban conditions.
W. Richard Leaitch, Alexei Korolev, Amir A. Aliabadi, Julia Burkart, Megan D. Willis, Jonathan P. D. Abbatt, Heiko Bozem, Peter Hoor, Franziska Köllner, Johannes Schneider, Andreas Herber, Christian Konrad, and Ralf Brauner
Atmos. Chem. Phys., 16, 11107–11124, https://doi.org/10.5194/acp-16-11107-2016, https://doi.org/10.5194/acp-16-11107-2016, 2016
Short summary
Short summary
Thought to be mostly unimportant for summertime Arctic liquid-water clouds, airborne observations show that atmospheric aerosol particles 50 nm in diameter or smaller and most likely from natural sources are often involved in cloud formation in the pristine Arctic summer. The result expands the reference for aerosol forcing of climate. Further, for extremely low droplet concentrations, no evidence is found for a connection between cloud liquid water and aerosol particle concentrations.
Amir A. Aliabadi, Jennie L. Thomas, Andreas B. Herber, Ralf M. Staebler, W. Richard Leaitch, Hannes Schulz, Kathy S. Law, Louis Marelle, Julia Burkart, Megan D. Willis, Heiko Bozem, Peter M. Hoor, Franziska Köllner, Johannes Schneider, Maurice Levasseur, and Jonathan P. D. Abbatt
Atmos. Chem. Phys., 16, 7899–7916, https://doi.org/10.5194/acp-16-7899-2016, https://doi.org/10.5194/acp-16-7899-2016, 2016
Short summary
Short summary
For the first time, ship emissions of an ice-breaker, the Amundsen, is characterized while breaking ice in the Canadian Arctic using the plume intercepts by the Polar 6 aircraft. The study is novel, estimating lower plume expansion rates over the stable Arctic marine boundary layer and different emissions factors for oxides of nitrogen, black carbon, and carbon monoxide, compared to plume intercept studies in mid latitudes. These results can inform policy making and emission inventory datasets.
Alex K. Y. Lee, Jonathan P. D. Abbatt, W. Richard Leaitch, Shao-Meng Li, Steve J. Sjostedt, Jeremy J. B. Wentzell, John Liggio, and Anne Marie Macdonald
Atmos. Chem. Phys., 16, 6721–6733, https://doi.org/10.5194/acp-16-6721-2016, https://doi.org/10.5194/acp-16-6721-2016, 2016
Short summary
Short summary
Substantial biogenic secondary organic aerosol (BSOA) formation was investigated in a coniferous forest mountain region in Whistler, British Columbia. A largely biogenic aerosol growth episode was observed, providing a unique opportunity to investigate BSOA formation chemistry in a forested environment. In particular, our observations provide insights into the relative importance of different oxidation mechanisms between day and night.
Betty Croft, Randall V. Martin, W. Richard Leaitch, Peter Tunved, Thomas J. Breider, Stephen D. D'Andrea, and Jeffrey R. Pierce
Atmos. Chem. Phys., 16, 3665–3682, https://doi.org/10.5194/acp-16-3665-2016, https://doi.org/10.5194/acp-16-3665-2016, 2016
Short summary
Short summary
Measurements at high-Arctic sites show a strong annual cycle in atmospheric particle number and size. Previous studies identified poor scientific understanding related to global model representation of Arctic particle number and size, limiting ability to simulate this environment. Here we evaluate state-of-science ability to simulate Arctic particles using GEOS-Chem-TOMAS model, documenting key roles and interconnections of particle formation, cloud-related processes and remaining uncertainties.
S. Gagné, L. P. MacDonald, W. R. Leaitch, and J. R. Pierce
Atmos. Meas. Tech., 9, 619–630, https://doi.org/10.5194/amt-9-619-2016, https://doi.org/10.5194/amt-9-619-2016, 2016
Short summary
Short summary
Measurements of clouds with an aircraft are essential to understand how clouds form and how they affect the Earth's climate. These measurements are used in climate models to help predict how our climate might develop in the next century. Aircraft measurements are, however, difficult for modellers to interpret because the way they were acquired and analyzed varies from one team of scientists to the next. We present a software platform for scientists to share and compare their analysis tools.
L. Kleinman, C. Kuang, A. Sedlacek, G. Senum, S. Springston, J. Wang, Q. Zhang, J. Jayne, J. Fast, J. Hubbe, J. Shilling, and R. Zaveri
Atmos. Chem. Phys., 16, 1729–1746, https://doi.org/10.5194/acp-16-1729-2016, https://doi.org/10.5194/acp-16-1729-2016, 2016
Short summary
Short summary
Atmospheric measurements of total organic aerosol (OA) and tracers of anthropogenic and biogenic emissions are used to quantify synergistic effects (A–B interactions) between two classes of precursors in the formation of OA. Regressions are consistent with the Sacramento plume composed mainly of modern carbon, and OA correlating best with an anthropogenic tracer. It is found that meteorological conditions during a pollution episode can mimic effects of A–B interactions.
R. H. Mason, M. Si, C. Chou, V. E. Irish, R. Dickie, P. Elizondo, R. Wong, M. Brintnell, M. Elsasser, W. M. Lassar, K. M. Pierce, W. R. Leaitch, A. M. MacDonald, A. Platt, D. Toom-Sauntry, R. Sarda-Estève, C. L. Schiller, K. J. Suski, T. C. J. Hill, J. P. D. Abbatt, J. A. Huffman, P. J. DeMott, and A. K. Bertram
Atmos. Chem. Phys., 16, 1637–1651, https://doi.org/10.5194/acp-16-1637-2016, https://doi.org/10.5194/acp-16-1637-2016, 2016
L. Xu, L. R. Williams, D. E. Young, J. D. Allan, H. Coe, P. Massoli, E. Fortner, P. Chhabra, S. Herndon, W. A. Brooks, J. T. Jayne, D. R. Worsnop, A. C. Aiken, S. Liu, K. Gorkowski, M. K. Dubey, Z. L. Fleming, S. Visser, A. S. H. Prévôt, and N. L. Ng
Atmos. Chem. Phys., 16, 1139–1160, https://doi.org/10.5194/acp-16-1139-2016, https://doi.org/10.5194/acp-16-1139-2016, 2016
Short summary
Short summary
We investigate the spatial distribution of submicron aerosol in the greater London area as part of the Clean Air for London (ClearfLo) project in winter 2012. Although the concentrations of organic aerosol (OA) are similar between a rural and an urban site, the OA sources are different. We also examine the volatility of submicron aerosol at the rural site and find that the non-volatile organics have similar sources or have undergone similar chemical processing as refractory black carbon.
S. D. D'Andrea, J. Y. Ng, J. K. Kodros, S. A. Atwood, M. J. Wheeler, A. M. Macdonald, W. R. Leaitch, and J. R. Pierce
Atmos. Chem. Phys., 16, 383–396, https://doi.org/10.5194/acp-16-383-2016, https://doi.org/10.5194/acp-16-383-2016, 2016
Short summary
Short summary
We evaluate aerosol size distributions predicted by GEOS-Chem-TOMAS using measurements from the peak of Whistler Mountain. We improve model-measurement comparisons of aerosol number, size, and composition during periods of free-tropospheric and boundary-layer influence by developing simple filtering techniques, and determine the influence of Asian anthropogenic and biomass burning emissions. The low-cost filtering techniques and source apportionment methods can be used for other mountain sites.
F. Yu, G. Luo, S. C. Pryor, P. R. Pillai, S. H. Lee, J. Ortega, J. J. Schwab, A. G. Hallar, W. R. Leaitch, V. P. Aneja, J. N. Smith, J. T. Walker, O. Hogrefe, and K. L. Demerjian
Atmos. Chem. Phys., 15, 13993–14003, https://doi.org/10.5194/acp-15-13993-2015, https://doi.org/10.5194/acp-15-13993-2015, 2015
Short summary
Short summary
The role of low-volatility organics in new particle formation (NPF) in the atmosphere is assessed. An empirical formulation in which formation rate is a function of the concentrations of sulfuric acid and low-volatility organics significantly overpredicts NPF in the summer.
Two different schemes predict quite different nucleation rates (including their spatial patterns), concentrations of cloud condensation nuclei, and aerosol first indirect radiative forcing in North America.
R. H. Mason, M. Si, J. Li, C. Chou, R. Dickie, D. Toom-Sauntry, C. Pöhlker, J. D. Yakobi-Hancock, L. A. Ladino, K. Jones, W. R. Leaitch, C. L. Schiller, J. P. D. Abbatt, J. A. Huffman, and A. K. Bertram
Atmos. Chem. Phys., 15, 12547–12566, https://doi.org/10.5194/acp-15-12547-2015, https://doi.org/10.5194/acp-15-12547-2015, 2015
E. Jung, B. A. Albrecht, H. H. Jonsson, Y.-C. Chen, J. H. Seinfeld, A. Sorooshian, A. R. Metcalf, S. Song, M. Fang, and L. M. Russell
Atmos. Chem. Phys., 15, 5645–5658, https://doi.org/10.5194/acp-15-5645-2015, https://doi.org/10.5194/acp-15-5645-2015, 2015
Short summary
Short summary
To study the effect of giant cloud condensation nuclei (GCCN) on precipitation processes in stratocumulus clouds, 1-10 µm diameter salt particles were released from an aircraft while flying near the cloud top off the central coast of California. The analyses suggest that GCCN result in a four-fold increase in the cloud base rainfall rate and depletion of the cloud water due to rainout.
J. C. Schroder, S. J. Hanna, R. L. Modini, A. L. Corrigan, S. M. Kreidenwies, A. M. Macdonald, K. J. Noone, L. M. Russell, W. R. Leaitch, and A. K. Bertram
Atmos. Chem. Phys., 15, 1367–1383, https://doi.org/10.5194/acp-15-1367-2015, https://doi.org/10.5194/acp-15-1367-2015, 2015
S. M. Burrows, O. Ogunro, A. A. Frossard, L. M. Russell, P. J. Rasch, and S. M. Elliott
Atmos. Chem. Phys., 14, 13601–13629, https://doi.org/10.5194/acp-14-13601-2014, https://doi.org/10.5194/acp-14-13601-2014, 2014
Short summary
Short summary
The air over the ocean is full of sea spray particles ejected by bubbles that burst in the wake of breaking waves. The smallest of such particles, less than a micrometer in diameter, include organic matter derived from ocean biota. This paper introduces a method to calculate the chemical composition of spray particles. Ocean organic matter is divided into several classes using a global model. Basic chemistry relationships predict the amount of organic material in emitted spray.
J. D. Yakobi-Hancock, L. A. Ladino, A. K. Bertram, J. A. Huffman, K. Jones, W. R. Leaitch, R. H. Mason, C. L. Schiller, D. Toom-Sauntry, J. P. S. Wong, and J. P. D. Abbatt
Atmos. Chem. Phys., 14, 12307–12317, https://doi.org/10.5194/acp-14-12307-2014, https://doi.org/10.5194/acp-14-12307-2014, 2014
Short summary
Short summary
As one aspect of the NETwork on Climate and Aerosols: addressing key uncertainties in Remote Canadian Environments, measurements of the cloud condensation nucleation properties of 50 nm and 100 nm aerosol particles were conducted at Ucluelet on the west coast of Vancouver Island in August 2013. The most efficient cloud condensation nuclei arose when the organic to sulfate ratio of the aerosol was lowest and when winds arrived from the west after transport through the marine boundary layer.
K. Tsigaridis, N. Daskalakis, M. Kanakidou, P. J. Adams, P. Artaxo, R. Bahadur, Y. Balkanski, S. E. Bauer, N. Bellouin, A. Benedetti, T. Bergman, T. K. Berntsen, J. P. Beukes, H. Bian, K. S. Carslaw, M. Chin, G. Curci, T. Diehl, R. C. Easter, S. J. Ghan, S. L. Gong, A. Hodzic, C. R. Hoyle, T. Iversen, S. Jathar, J. L. Jimenez, J. W. Kaiser, A. Kirkevåg, D. Koch, H. Kokkola, Y. H Lee, G. Lin, X. Liu, G. Luo, X. Ma, G. W. Mann, N. Mihalopoulos, J.-J. Morcrette, J.-F. Müller, G. Myhre, S. Myriokefalitakis, N. L. Ng, D. O'Donnell, J. E. Penner, L. Pozzoli, K. J. Pringle, L. M. Russell, M. Schulz, J. Sciare, Ø. Seland, D. T. Shindell, S. Sillman, R. B. Skeie, D. Spracklen, T. Stavrakou, S. D. Steenrod, T. Takemura, P. Tiitta, S. Tilmes, H. Tost, T. van Noije, P. G. van Zyl, K. von Salzen, F. Yu, Z. Wang, Z. Wang, R. A. Zaveri, H. Zhang, K. Zhang, Q. Zhang, and X. Zhang
Atmos. Chem. Phys., 14, 10845–10895, https://doi.org/10.5194/acp-14-10845-2014, https://doi.org/10.5194/acp-14-10845-2014, 2014
J. D. Fast, J. Allan, R. Bahreini, J. Craven, L. Emmons, R. Ferrare, P. L. Hayes, A. Hodzic, J. Holloway, C. Hostetler, J. L. Jimenez, H. Jonsson, S. Liu, Y. Liu, A. Metcalf, A. Middlebrook, J. Nowak, M. Pekour, A. Perring, L. Russell, A. Sedlacek, J. Seinfeld, A. Setyan, J. Shilling, M. Shrivastava, S. Springston, C. Song, R. Subramanian, J. W. Taylor, V. Vinoj, Q. Yang, R. A. Zaveri, and Q. Zhang
Atmos. Chem. Phys., 14, 10013–10060, https://doi.org/10.5194/acp-14-10013-2014, https://doi.org/10.5194/acp-14-10013-2014, 2014
J. R. Pierce, D. M. Westervelt, S. A. Atwood, E. A. Barnes, and W. R. Leaitch
Atmos. Chem. Phys., 14, 8647–8663, https://doi.org/10.5194/acp-14-8647-2014, https://doi.org/10.5194/acp-14-8647-2014, 2014
S. Gilardoni, P. Massoli, L. Giulianelli, M. Rinaldi, M. Paglione, F. Pollini, C. Lanconelli, V. Poluzzi, S. Carbone, R. Hillamo, L. M. Russell, M. C. Facchini, and S. Fuzzi
Atmos. Chem. Phys., 14, 6967–6981, https://doi.org/10.5194/acp-14-6967-2014, https://doi.org/10.5194/acp-14-6967-2014, 2014
J. Kangasluoma, C. Kuang, D. Wimmer, M. P. Rissanen, K. Lehtipalo, M. Ehn, D. R. Worsnop, J. Wang, M. Kulmala, and T. Petäjä
Atmos. Meas. Tech., 7, 689–700, https://doi.org/10.5194/amt-7-689-2014, https://doi.org/10.5194/amt-7-689-2014, 2014
A. Steffen, J. Bottenheim, A. Cole, R. Ebinghaus, G. Lawson, and W. R. Leaitch
Atmos. Chem. Phys., 14, 2219–2231, https://doi.org/10.5194/acp-14-2219-2014, https://doi.org/10.5194/acp-14-2219-2014, 2014
B. H. Kahn, F. W. Irion, V. T. Dang, E. M. Manning, S. L. Nasiri, C. M. Naud, J. M. Blaisdell, M. M. Schreier, Q. Yue, K. W. Bowman, E. J. Fetzer, G. C. Hulley, K. N. Liou, D. Lubin, S. C. Ou, J. Susskind, Y. Takano, B. Tian, and J. R. Worden
Atmos. Chem. Phys., 14, 399–426, https://doi.org/10.5194/acp-14-399-2014, https://doi.org/10.5194/acp-14-399-2014, 2014
A. L. Corrigan, L. M. Russell, S. Takahama, M. Äijälä, M. Ehn, H. Junninen, J. Rinne, T. Petäjä, M. Kulmala, A. L. Vogel, T. Hoffmann, C. J. Ebben, F. M. Geiger, P. Chhabra, J. H. Seinfeld, D. R. Worsnop, W. Song, J. Auld, and J. Williams
Atmos. Chem. Phys., 13, 12233–12256, https://doi.org/10.5194/acp-13-12233-2013, https://doi.org/10.5194/acp-13-12233-2013, 2013
S. D. D'Andrea, S. A. K. Häkkinen, D. M. Westervelt, C. Kuang, E. J. T. Levin, V. P. Kanawade, W. R. Leaitch, D. V. Spracklen, I. Riipinen, and J. R. Pierce
Atmos. Chem. Phys., 13, 11519–11534, https://doi.org/10.5194/acp-13-11519-2013, https://doi.org/10.5194/acp-13-11519-2013, 2013
A. L. Vogel, M. Äijälä, A. L. Corrigan, H. Junninen, M. Ehn, T. Petäjä, D. R. Worsnop, M. Kulmala, L. M. Russell, J. Williams, and T. Hoffmann
Atmos. Chem. Phys., 13, 10933–10950, https://doi.org/10.5194/acp-13-10933-2013, https://doi.org/10.5194/acp-13-10933-2013, 2013
A. Wonaschütz, M. Coggon, A. Sorooshian, R. Modini, A. A. Frossard, L. Ahlm, J. Mülmenstädt, G. C. Roberts, L. M. Russell, S. Dey, F. J. Brechtel, and J. H. Seinfeld
Atmos. Chem. Phys., 13, 9819–9835, https://doi.org/10.5194/acp-13-9819-2013, https://doi.org/10.5194/acp-13-9819-2013, 2013
E. Kostenidou, C. Kaltsonoudis, M. Tsiflikiotou, E. Louvaris, L. M. Russell, and S. N. Pandis
Atmos. Chem. Phys., 13, 8797–8811, https://doi.org/10.5194/acp-13-8797-2013, https://doi.org/10.5194/acp-13-8797-2013, 2013
M. D. Gibson, J. R. Pierce, D. Waugh, J. S. Kuchta, L. Chisholm, T. J. Duck, J. T. Hopper, S. Beauchamp, G. H. King, J. E. Franklin, W. R. Leaitch, A. J. Wheeler, Z. Li, G. A. Gagnon, and P. I. Palmer
Atmos. Chem. Phys., 13, 7199–7213, https://doi.org/10.5194/acp-13-7199-2013, https://doi.org/10.5194/acp-13-7199-2013, 2013
J. Wang, R. L. McGraw, and C. Kuang
Atmos. Chem. Phys., 13, 6523–6531, https://doi.org/10.5194/acp-13-6523-2013, https://doi.org/10.5194/acp-13-6523-2013, 2013
B. Ervens, Y. Wang, J. Eagar, W. R. Leaitch, A. M. Macdonald, K. T. Valsaraj, and P. Herckes
Atmos. Chem. Phys., 13, 5117–5135, https://doi.org/10.5194/acp-13-5117-2013, https://doi.org/10.5194/acp-13-5117-2013, 2013
L. Ahlm, K. M. Shakya, L. M. Russell, J. C. Schroder, J. P. S. Wong, S. J. Sjostedt, K. L. Hayden, J. Liggio, J. J. B. Wentzell, H. A. Wiebe, C. Mihele, W. R. Leaitch, and A. M. Macdonald
Atmos. Chem. Phys., 13, 3393–3407, https://doi.org/10.5194/acp-13-3393-2013, https://doi.org/10.5194/acp-13-3393-2013, 2013
Related subject area
Subject: Aerosols | Research Activity: Field Measurements | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Opinion: How will advances in aerosol science inform our understanding of the health impacts of outdoor particulate pollution?
Measurement report: Intra-annual variability of black carbon and brown carbon and their interrelation with meteorological conditions over Gangtok, Sikkim
Long-range transport of air pollutants increases the concentration of hazardous components of PM2.5 in northern South America
Dominant influence of biomass combustion and cross-border transport on nitrogen-containing organic compound levels in the southeastern Tibetan Plateau
Impacts of elevated anthropogenic emissions on physicochemical characteristics of black-carbon-containing particles over the Tibetan Plateau
Online characterization of primary and secondary emissions of particulate matter and acidic molecules from a modern fleet of city buses
Atmospheric evolution of environmentally persistent free radicals in the rural North China Plain: effects on water solubility and PM2.5 oxidative potential
Two distinct ship emission profiles for organic-sulfate source apportionment of PM in sulfur emission control areas
Automated compound speciation, cluster analysis, and quantification of organic vapors and aerosols using comprehensive two-dimensional gas chromatography and mass spectrometry
Measurement report: Occurrence of aminiums in PM2.5 during winter in China – aminium outbreak during polluted episodes and potential constraints
Bridging gas and aerosol properties between the northeastern US and Bermuda: analysis of eight transit flights
The behaviour of charged particles (ions) during new particle formation events in urban Leipzig, Germany
Exploring the sources of light-absorbing carbonaceous aerosols by integrating observational and modeling results: insights from Northeast China
Measurement report: Characteristics of airborne black-carbon-containing particles during the 2021 summer COVID-19 lockdown in a typical Yangtze River Delta city, China
Aerosol optical properties within the atmospheric boundary layer predicted from ground-based observations compared to Raman lidar retrievals during RITA-2021
Hygroscopic growth and activation changed submicron aerosol composition and properties in the North China Plain
Measurement report: Formation of tropospheric brown carbon in a lifting air mass
Vertical variability of aerosol properties and trace gases over a remote marine region: a case study over Bermuda
Differences in aerosol and cloud properties along the central California coast when winds change from northerly to southerly
International airport emissions and their impact on local air quality: chemical speciation of ambient aerosols at Madrid–Barajas Airport during the AVIATOR campaign
Significant role of biomass burning in heavy haze formation in a megacity: Molecular-level insights from intensive PM2.5 sampling on winter hazy days
The local ship speed reduction effect on black carbon emissions measured at a remote marine station
High-altitude aerosol chemical characterization and source identification: insights from the CALISHTO campaign
Measurement report: Impact of emission control measures on environmental persistent free radicals and reactive oxygen species – a short-term case study in Beijing
Characterizing water solubility of fresh and aged secondary organic aerosol in PM2.5 with the stable carbon isotope technique
Measurement report: Impact of cloud processes on secondary organic aerosols at a forested mountain site in southeastern China
Critical contribution of chemically diverse carbonyl molecules to the oxidative potential of atmospheric aerosols
Seasonal Investigation of Ultrafine Particle Composition in an Eastern Amazonian Rainforest
Measurement report: Vanadium-containing ship exhaust particles detected in and above the marine boundary layer in the remote atmosphere
Diverging trends in aerosol sulfate and nitrate measured in the remote North Atlantic in Barbados are attributed to clean air policies, African smoke, and anthropogenic emissions
Technical note: Quantified organic aerosol subsaturated hygroscopicity by a simple optical scatter monitor system through field measurements
Diverse sources and aging change the mixing state and ice nucleation properties of aerosol particles over the western Pacific and Southern Ocean
The water-insoluble organic carbon in PM2.5 of typical Chinese urban areas: light-absorbing properties, potential sources, radiative forcing effects, and a possible light-absorbing continuum
Measurement report: Size-resolved secondary organic aerosol formation modulated by aerosol water uptake in wintertime haze
In situ measurement of organic aerosol molecular markers in urban Hong Kong during a summer period: temporal variations and source apportionment
Technical note: Determining chemical composition of atmospheric single particles by a standard-free mass calibration algorithm
Different formation pathways of nitrogen-containing organic compounds in aerosols and fog water in northern China
Impact of weather patterns and meteorological factors on PM2.5 and O3 responses to the COVID-19 lockdown in China
Daytime and nighttime aerosol soluble iron formation in clean and slightly polluted moist air in a coastal city in eastern China
Non-negligible secondary contribution to brown carbon in autumn and winter: inspiration from particulate nitrated and oxygenated aromatic compounds in urban Beijing
A Multi-site Passive Approach for Studying the Emissions and Evolution of Smoke from Prescribed Fires
Non-sea-salt aerosols that contain trace bromine and iodine are widespread in the remote troposphere
Simultaneous organic aerosol source apportionment at two Antarctic sites reveals large-scale and ecoregion-specific components
Measurement report: Optical characterization, seasonality, and sources of brown carbon in fine aerosols from Tianjin, North China: year-round observations
High-resolution analyses of concentrations and sizes of black carbon particles deposited on northwest Greenland over the past 350 years – Part 2: Seasonal and temporal trends in black carbon originated from fossil fuel combustion and biomass burning
Bayesian inference-based estimation of hourly primary and secondary organic carbon in suburban Hong Kong: multi-temporal-scale variations and evolution characteristics during PM2.5 episodes
Formation and chemical evolution of SOA in two different environments: A dual chamber study
Enhanced daytime secondary aerosol formation driven by gas-particle partitioning in downwind urban plumes
Multiple eco-regions contribute to the seasonal cycle of Antarctic aerosol size distributions
Impact assessment of terrestrial and marine air-mass on the constituents and intermixing of bioaerosols over coastal atmosphere
Imad El Haddad, Danielle Vienneau, Kaspar R. Daellenbach, Robin Modini, Jay G. Slowik, Abhishek Upadhyay, Petros N. Vasilakos, David Bell, Kees de Hoogh, and Andre S. H. Prevot
Atmos. Chem. Phys., 24, 11981–12011, https://doi.org/10.5194/acp-24-11981-2024, https://doi.org/10.5194/acp-24-11981-2024, 2024
Short summary
Short summary
This opinion paper explores how advances in aerosol science inform our understanding of the health impacts of outdoor particulate pollution. We advocate for a shift in the way we target PM pollution, focusing on the most harmful anthropogenic emissions. We highlight key observations, modelling developments, and emission measurements needed to achieve this shift.
Pramod Kumar, Khushboo Sharma, Ankita Malu, Rajeev Rajak, Aparna Gupta, Bidyutjyoti Baruah, Shailesh Yadav, Thupstan Angchuk, Jayant Sharma, Rakesh Kumar Ranjan, Anil Kumar Misra, and Nishchal Wanjari
Atmos. Chem. Phys., 24, 11585–11601, https://doi.org/10.5194/acp-24-11585-2024, https://doi.org/10.5194/acp-24-11585-2024, 2024
Short summary
Short summary
This work monitors and assesses air pollution, especially black and brown carbon, its controlling factor, and its effect on the environment of Sikkim Himalayan region. The huge urban sprawl in recent decades has led to regional human-induced air pollution in the region. Black carbon was highest in April 2021 and March 2022, exceeding the WHO limit. The monsoon season causes huge rainfall over the region, which reduces the pollutants by scavenging (rainout and washout).
Maria P. Velásquez-García, K. Santiago Hernández, James A. Vergara-Correa, Richard J. Pope, Miriam Gómez-Marín, and Angela M. Rendón
Atmos. Chem. Phys., 24, 11497–11520, https://doi.org/10.5194/acp-24-11497-2024, https://doi.org/10.5194/acp-24-11497-2024, 2024
Short summary
Short summary
In the Aburrá Valley, northern South America, local emissions determine air quality conditions. However, we found that external sources, such as regional fires, Saharan dust, and volcanic emissions, increase particulate concentrations and worsen chemical composition by introducing elements like heavy metals. Dry winds and source variability contribute to seasonal influences on these events. This study assesses the air quality risks posed by such events, which can affect broad regions worldwide.
Meng Wang, Qiyuan Wang, Steven Sai Hang Ho, Jie Tian, Yong Zhang, Shun-cheng Lee, and Junji Cao
Atmos. Chem. Phys., 24, 11175–11189, https://doi.org/10.5194/acp-24-11175-2024, https://doi.org/10.5194/acp-24-11175-2024, 2024
Short summary
Short summary
We studied nitrogen-containing organic compounds (NOCs) in particulate matter <2.5 µm particles on the southeastern Tibetan Plateau. We found that biomass burning and transboundary transport are the main sources of NOCs in the high-altitude area. Understanding these aerosol sources informs how they add to regional and potentially global climate changes. Our findings could help shape effective environmental policies to enhance air quality and address climate impacts in this sensitive region.
Jinbo Wang, Jiaping Wang, Yuxuan Zhang, Tengyu Liu, Xuguang Chi, Xin Huang, Dafeng Ge, Shiyi Lai, Caijun Zhu, Lei Wang, Qiaozhi Zha, Ximeng Qi, Wei Nie, Congbin Fu, and Aijun Ding
Atmos. Chem. Phys., 24, 11063–11080, https://doi.org/10.5194/acp-24-11063-2024, https://doi.org/10.5194/acp-24-11063-2024, 2024
Short summary
Short summary
In this study, we found large spatial discrepancies in the physical and chemical properties of black carbon over the Tibetan Plateau (TP). Elevated anthropogenic emissions from low-altitude regions can significantly change the mass concentration, mixing state and chemical composition of black-carbon-containing aerosol in the TP region, further altering its light absorption ability. Our study emphasizes the vulnerability of remote plateau regions to intense anthropogenic influences.
Liyuan Zhou, Qianyun Liu, Christian M. Salvador, Michael Le Breton, Mattias Hallquist, Jian Zhen Yu, Chak K. Chan, and Åsa M. Hallquist
Atmos. Chem. Phys., 24, 11045–11061, https://doi.org/10.5194/acp-24-11045-2024, https://doi.org/10.5194/acp-24-11045-2024, 2024
Short summary
Short summary
Our research on city bus emissions reveals that alternative fuels (compressed natural gas and biofuels) reduce fresh particle emissions compared to diesel. However, all fuels lead to secondary air pollution. Aiming at guiding better environmental policies, we studied 76 buses using advanced emission measurement techniques. This work sheds light on the complex effects of bus fuels on urban air quality, emphasizing the need for comprehensive evaluations of future transportation technologies.
Xu Yang, Fobang Liu, Shuqi Yang, Yuling Yang, Yanan Wang, Jingjing Li, Mingyu Zhao, Zhao Wang, Kai Wang, Chi He, and Haijie Tong
Atmos. Chem. Phys., 24, 11029–11043, https://doi.org/10.5194/acp-24-11029-2024, https://doi.org/10.5194/acp-24-11029-2024, 2024
Short summary
Short summary
A study in the rural North China Plain showed environmentally persistent free radicals (EPFRs) in atmospheric particulate matter (PM), with a notable water-soluble fraction likely from atmospheric oxidation during transport. Significant positive correlations between EPFRs and the water-soluble oxidative potential of PM2.5 were found, primarily attributable to the water-soluble fractions of EPFRs. These findings emphasize understanding EPFRs' atmospheric evolution for climate and health impacts.
Kirsten N. Fossum, Chunshui Lin, Niall O'Sullivan, Lu Lei, Stig Hellebust, Darius Ceburnis, Aqeel Afzal, Anja Tremper, David Green, Srishti Jain, Steigvilė Byčenkienė, Colin O'Dowd, John Wenger, and Jurgita Ovadnevaite
Atmos. Chem. Phys., 24, 10815–10831, https://doi.org/10.5194/acp-24-10815-2024, https://doi.org/10.5194/acp-24-10815-2024, 2024
Short summary
Short summary
The chemical composition and sources of submicron aerosol in the Dublin Port area were investigated over a month-long campaign. Two distinct types of ship emissions were identified and characterised: sulfate-rich plumes from the use of heavy fuel oil with scrubbers and organic-rich plumes from the use of low-sulfur fuels. The latter were more frequent, emitting double the particle number and having a typical V / Ni ratio for ship emission.
Xiao He, Xuan Zheng, Shuwen Guo, Lewei Zeng, Ting Chen, Bohan Yang, Shupei Xiao, Qiongqiong Wang, Zhiyuan Li, Yan You, Shaojun Zhang, and Ye Wu
Atmos. Chem. Phys., 24, 10655–10666, https://doi.org/10.5194/acp-24-10655-2024, https://doi.org/10.5194/acp-24-10655-2024, 2024
Short summary
Short summary
This study introduces an innovative method for identifying and quantifying complex organic vapors and aerosols. By combining advanced analytical techniques and new algorithms, we categorized thousands of compounds from heavy-duty diesel vehicles and ambient air and highlighted specific tracers for emission sources. The innovative approach enhances peak identification, reduces quantification uncertainties, and offers new insights for air quality management and atmospheric chemistry.
Yu Xu, Tang Liu, Yi-Jia Ma, Qi-Bin Sun, Hong-Wei Xiao, Hao Xiao, Hua-Yun Xiao, and Cong-Qiang Liu
Atmos. Chem. Phys., 24, 10531–10542, https://doi.org/10.5194/acp-24-10531-2024, https://doi.org/10.5194/acp-24-10531-2024, 2024
Short summary
Short summary
This study investigates the characteristics of aminiums and ammonium in PM2.5 on clean and polluted winter days in 11 Chinese cities, highlighting the possibility of the competitive uptake of ammonia versus amines on acidic aerosols or the displacement of aminiums by ammonia under high-ammonia conditions. The overall results deepen the understanding of the spatiotemporal differences in aminium characteristics and formation in China.
Cassidy Soloff, Taiwo Ajayi, Yonghoon Choi, Ewan C. Crosbie, Joshua P. DiGangi, Glenn S. Diskin, Marta A. Fenn, Richard A. Ferrare, Francesca Gallo, Johnathan W. Hair, Miguel Ricardo A. Hilario, Simon Kirschler, Richard H. Moore, Taylor J. Shingler, Michael A. Shook, Kenneth L. Thornhill, Christiane Voigt, Edward L. Winstead, Luke D. Ziemba, and Armin Sorooshian
Atmos. Chem. Phys., 24, 10385–10408, https://doi.org/10.5194/acp-24-10385-2024, https://doi.org/10.5194/acp-24-10385-2024, 2024
Short summary
Short summary
Using aircraft measurements over the northwestern Atlantic between the US East Coast and Bermuda and trajectory modeling of continental outflow, we identify trace gas and particle properties that exhibit gradients with offshore distance and quantify these changes with high-resolution measurements of concentrations and particle chemistry, size, and scattering properties. This work furthers our understanding of the complex interactions between continental and marine environments.
Alex Rowell, James Brean, David C. S. Beddows, Zongbo Shi, Avinash Kumar, Matti Rissanen, Miikka Dal Maso, Peter Mettke, Kay Weinhold, Maik Merkel, and Roy M. Harrison
Atmos. Chem. Phys., 24, 10349–10361, https://doi.org/10.5194/acp-24-10349-2024, https://doi.org/10.5194/acp-24-10349-2024, 2024
Short summary
Short summary
Ions enhance the formation and growth rates of new particles, affecting the Earth's radiation budget. Despite these effects, there is little published data exploring the sources of ions in the urban environment and their role in new particle formation (NPF). Here we show that natural ion sources dominate in urban environments, while traffic is a secondary source. Ions contribute up to 12.7 % of the formation rate of particles, indicating that they are important for forming urban PM.
Yuan Cheng, Xu-bing Cao, Sheng-qiang Zhu, Zhi-qing Zhang, Jiu-meng Liu, Hong-liang Zhang, Qiang Zhang, and Ke-bin He
Atmos. Chem. Phys., 24, 9869–9883, https://doi.org/10.5194/acp-24-9869-2024, https://doi.org/10.5194/acp-24-9869-2024, 2024
Short summary
Short summary
The agreement between observational and modeling results is essential for the development of efficient air pollution control strategies. Here we constrained the modeling results of carbonaceous aerosols by field observation in Northeast China, a historically overlooked but recently targeted region of national clean-air actions. Our study suggested that the simulation of agricultural fire emissions and secondary organic aerosols remains challenging.
Yuan Dai, Junfeng Wang, Houjun Wang, Shijie Cui, Yunjiang Zhang, Haiwei Li, Yun Wu, Ming Wang, Eleonora Aruffo, and Xinlei Ge
Atmos. Chem. Phys., 24, 9733–9748, https://doi.org/10.5194/acp-24-9733-2024, https://doi.org/10.5194/acp-24-9733-2024, 2024
Short summary
Short summary
Short-term strict emission control can improve air quality, but its effectiveness needs assessment. During the 2021 summer COVID-19 lockdown in Yangzhou, we found that PM2.5 levels did not decrease despite reduced primary emissions. Aged black-carbon particles increased substantially due to higher O3 levels and transported pollutants. High humidity and low wind also played key roles. The results highlight the importance of a regionally balanced control strategy for future air quality management.
Xinya Liu, Diego Alves Gouveia, Bas Henzing, Arnoud Apituley, Arjan Hensen, Danielle van Dinther, Rujin Huang, and Ulrike Dusek
Atmos. Chem. Phys., 24, 9597–9614, https://doi.org/10.5194/acp-24-9597-2024, https://doi.org/10.5194/acp-24-9597-2024, 2024
Short summary
Short summary
The vertical distribution of aerosol optical properties is important for their effect on climate. This is usually measured by lidar, which has limitations, most notably the assumption of a lidar ratio. Our study shows that routine surface-level aerosol measurements are able to predict this lidar ratio reasonably well within the lower layers of the atmosphere and thus provide a relatively simple and cost-effective method to improve lidar measurements.
Weiqi Xu, Ye Kuang, Wanyun Xu, Zhiqiang Zhang, Biao Luo, Xiaoyi Zhang, Jiangchuang Tao, Hongqin Qiao, Li Liu, and Yele Sun
Atmos. Chem. Phys., 24, 9387–9399, https://doi.org/10.5194/acp-24-9387-2024, https://doi.org/10.5194/acp-24-9387-2024, 2024
Short summary
Short summary
We deployed an advanced aerosol–fog sampling system at a rural site in the North China Plain to investigate impacts of aerosol hygroscopic growth and activation on the physicochemical properties of submicron aerosols. Observed results highlighted remarkably different aqueous processing of primary and secondary submicron aerosol components under distinct ambient relative humidity (RH) conditions and that RH levels significantly impact aerosol sampling through the aerosol swelling effect.
Can Wu, Xiaodi Liu, Ke Zhang, Si Zhang, Cong Cao, Jianjun Li, Rui Li, Fan Zhang, and Gehui Wang
Atmos. Chem. Phys., 24, 9263–9275, https://doi.org/10.5194/acp-24-9263-2024, https://doi.org/10.5194/acp-24-9263-2024, 2024
Short summary
Short summary
Brown carbon (BrC) is prevalent in the troposphere and can efficiently absorb solar and terrestrial radiation. Our observations show that the enhanced light absorption of BrC relative to black carbon at the tropopause can be attributed to the formation of nitrogen-containing organic compounds through the aqueous-phase reactions of carbonyls with ammonium.
Taiwo Ajayi, Yonghoon Choi, Ewan C. Crosbie, Joshua P. DiGangi, Glenn S. Diskin, Marta A. Fenn, Richard A. Ferrare, Johnathan W. Hair, Miguel Ricardo A. Hilario, Chris A. Hostetler, Simon Kirschler, Richard H. Moore, Taylor J. Shingler, Michael A. Shook, Cassidy Soloff, Kenneth L. Thornhill, Christiane Voigt, Edward L. Winstead, Luke D. Ziemba, and Armin Sorooshian
Atmos. Chem. Phys., 24, 9197–9218, https://doi.org/10.5194/acp-24-9197-2024, https://doi.org/10.5194/acp-24-9197-2024, 2024
Short summary
Short summary
This study uses airborne data to examine vertical profiles of trace gases, aerosol particles, and meteorological variables over a remote marine area (Bermuda). Results show distinct differences based on both air mass source region (North America, Ocean, Caribbean/North Africa) and altitude for a given air mass type. This work highlights the sensitivity of remote marine areas to long-range transport and the importance of considering the vertical dependence of trace gas and aerosol properties.
Kira Zeider, Grace Betito, Anthony Bucholtz, Peng Xian, Annette Walker, and Armin Sorooshian
Atmos. Chem. Phys., 24, 9059–9083, https://doi.org/10.5194/acp-24-9059-2024, https://doi.org/10.5194/acp-24-9059-2024, 2024
Short summary
Short summary
The predominant wind direction along the California coast (northerly) reverses several times during the summer (to southerly). The effects of these wind reversals on aerosol and cloud characteristics are not well understood. Using data from multiple datasets we found that southerly flow periods had enhanced signatures of anthropogenic emissions due to shipping and continental sources, and clouds had more but smaller droplets.
Saleh Alzahrani, Doğuşhan Kılıç, Michael Flynn, Paul I. Williams, and James Allan
Atmos. Chem. Phys., 24, 9045–9058, https://doi.org/10.5194/acp-24-9045-2024, https://doi.org/10.5194/acp-24-9045-2024, 2024
Short summary
Short summary
This paper investigates emissions from aviation activities at an international airport to evaluate their impact on local air quality. The study provides detailed insights into the chemical composition of aerosols and key pollutants in the airport environment. Source apportionment analysis using positive matrix factorisation (PMF) identified three significant sources: less oxidised oxygenated organic aerosol, alkane organic aerosol, and more oxidised oxygenated organic aerosol.
Mingjie Kang, Mengying Bao, Wenhuai Song, Aduburexiati Abulimiti, Fang Cao, Sönke Szidat, and Yanlin Zhang
EGUsphere, https://doi.org/10.5194/egusphere-2024-2098, https://doi.org/10.5194/egusphere-2024-2098, 2024
Short summary
Short summary
Reports on the molecular level knowledge of high temporal resolution PM2.5 components on hazy days are still limited. This study investigated many individual PM2.5 species and sources. The results show biomass burning (BB) was the main source of organic carbon. Moreover, BB enhanced fungal spore emissions and secondary aerosol formation. The contribution of non-fossils increased with increasing haze pollution. These findings suggest BB may be an important driver of haze events in winter.
Mikko Heikkilä, Krista Luoma, Timo Mäkelä, and Tiia Grönholm
Atmos. Chem. Phys., 24, 8927–8941, https://doi.org/10.5194/acp-24-8927-2024, https://doi.org/10.5194/acp-24-8927-2024, 2024
Short summary
Short summary
Black carbon (BC) concentration was measured from 211 ship exhaust gas plumes at a remote marine station. Emission factors of BC were calculated in grams per kilogram of fuel. Ships with an exhaust gas cleaning system (EGCS) were found to have median BC emissions per fuel consumed 5 times lower than ships without an EGCS. However, this might be because of non-EGCS ships running at low engine loads rather than the EGCS itself. A local speed restriction would increase BC emissions of ships.
Olga Zografou, Maria Gini, Prodromos Fetfatzis, Konstantinos Granakis, Romanos Foskinis, Manousos Ioannis Manousakas, Fotios Tsopelas, Evangelia Diapouli, Eleni Dovrou, Christina N. Vasilakopoulou, Alexandros Papayannis, Spyros N. Pandis, Athanasios Nenes, and Konstantinos Eleftheriadis
Atmos. Chem. Phys., 24, 8911–8926, https://doi.org/10.5194/acp-24-8911-2024, https://doi.org/10.5194/acp-24-8911-2024, 2024
Short summary
Short summary
Characterization of PM1 and positive matrix factorization (PMF) source apportionment of organic and inorganic fractions were conducted at the high-altitude station (HAC)2. Cloud presence reduced PM1, affecting sulfate more than organics. Free-troposphere (FT) conditions showed more black carbon (eBC) than planetary boundary layer (PBL) conditions.
Yuanyuan Qin, Xinghua Zhang, Wei Huang, Juanjuan Qin, Xiaoyu Hu, Yuxuan Cao, Tianyi Zhao, Yang Zhang, Jihua Tan, Ziyin Zhang, Xinming Wang, and Zhenzhen Wang
Atmos. Chem. Phys., 24, 8737–8750, https://doi.org/10.5194/acp-24-8737-2024, https://doi.org/10.5194/acp-24-8737-2024, 2024
Short summary
Short summary
Environmental persistent free radicals (EPFRs) and reactive oxygen species (ROSs) play an active role in the atmosphere. Despite control measures having effectively reduced their emissions, reductions were less than in PM2.5. Emission control measures performed well in achieving Parade Blue, but reducing the impact of the atmosphere on human health remains challenging. Thus, there is a need to reassess emission control measures to better address the challenges posed by EPFRs and ROSs.
Fenghua Wei, Xing Peng, Liming Cao, Mengxue Tang, Ning Feng, Xiaofeng Huang, and Lingyan He
Atmos. Chem. Phys., 24, 8507–8518, https://doi.org/10.5194/acp-24-8507-2024, https://doi.org/10.5194/acp-24-8507-2024, 2024
Short summary
Short summary
The water solubility of secondary organic aerosols (SOAs) is a crucial factor in determining their hygroscopicity and climatic impact. Stable carbon isotope and mass spectrometry techniques were combined to assess the water solubility of SOAs with different aging degrees in a coastal megacity in China. This work revealed a much higher water-soluble fraction of aged SOA compared to fresh SOA, indicating that the aging degree of SOA has considerable impacts on its water solubility.
Zijun Zhang, Weiqi Xu, Yi Zhang, Wei Zhou, Xiangyu Xu, Aodong Du, Yinzhou Zhang, Hongqin Qiao, Ye Kuang, Xiaole Pan, Zifa Wang, Xueling Cheng, Lanzhong Liu, Qingyan Fu, Douglas R. Worsnop, Jie Li, and Yele Sun
Atmos. Chem. Phys., 24, 8473–8488, https://doi.org/10.5194/acp-24-8473-2024, https://doi.org/10.5194/acp-24-8473-2024, 2024
Short summary
Short summary
We investigated aerosol composition and sources and the interaction between secondary organic aerosol (SOA) and clouds at a regional mountain site in southeastern China. Clouds efficiently scavenge more oxidized SOA; however, cloud evaporation leads to the production of less oxidized SOA. The unexpectedly high presence of nitrate in aerosol particles indicates that nitrate formed in polluted areas has undergone interactions with clouds, significantly influencing the regional background site.
Feifei Li, Shanshan Tang, Jitao Lv, Shiyang Yu, Xu Sun, Dong Cao, Yawei Wang, and Guibin Jiang
Atmos. Chem. Phys., 24, 8397–8411, https://doi.org/10.5194/acp-24-8397-2024, https://doi.org/10.5194/acp-24-8397-2024, 2024
Short summary
Short summary
Targeted derivatization and non-targeted analysis with Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) were used to reveal the molecular composition of carbonyl molecules in PM2.5, and the important role of carbonyls in increasing the oxidative potential of organic aerosol was found in real samples.
Adam E. Thomas, Hayley S. Glicker, Alex B. Guenther, Roger Seco, Oscar Vega Bustillos, Julio Tota, Rodrigo A. F. Souza, and James N. Smith
EGUsphere, https://doi.org/10.5194/egusphere-2024-2230, https://doi.org/10.5194/egusphere-2024-2230, 2024
Short summary
Short summary
We present measurements of the composition of ultrafine particles collected from the eastern Amazon, a relatively understudied region that is subjected to increasing human influence. We find that while isoprene chemistry is likely significant to ultrafine particle growth throughout the year, compounds related to other sources such as biological spore emissions and biomass burning exhibit striking seasonal differences, implying an extensive variation in regional ultrafine particle sources.
Maya Abou-Ghanem, Daniel M. Murphy, Gregory P. Schill, Michael J. Lawler, and Karl D. Froyd
Atmos. Chem. Phys., 24, 8263–8275, https://doi.org/10.5194/acp-24-8263-2024, https://doi.org/10.5194/acp-24-8263-2024, 2024
Short summary
Short summary
Using particle analysis by laser mass spectrometry, we examine vanadium-containing ship exhaust particles measured on NASA's DC-8 during the Atmospheric Tomography Mission (ATom). Our results reveal ship exhaust particles are sufficiently widespread in the marine atmosphere and experience atmospheric aging. Finally, we use laboratory calibrations to determine the vanadium, sulfate, and organic single-particle mass fractions of vanadium-containing ship exhaust particles.
Cassandra J. Gaston, Joseph M. Prospero, Kristen Foley, Havala O. T. Pye, Lillian Custals, Edmund Blades, Peter Sealy, and James A. Christie
Atmos. Chem. Phys., 24, 8049–8066, https://doi.org/10.5194/acp-24-8049-2024, https://doi.org/10.5194/acp-24-8049-2024, 2024
Short summary
Short summary
To understand how changing emissions have impacted aerosols in remote regions, we measured nitrate and sulfate in Barbados and compared them to model predictions from EPA’s Air QUAlity TimE Series (EQUATES). Nitrate was stable, except for spikes in 2008 and 2010 due to transported smoke. Sulfate decreased in the 1990s due to reductions in sulfur dioxide (SO2) in the US and Europe; then it increased in the 2000s, likely due to anthropogenic emissions from Africa.
Jie Zhang, Tianyu Zhu, Alexandra Catena, Yaowei Li, Margaret Schwab, Pengfei Liu, Akua Asa-Awuku, and James Schwab
EGUsphere, https://doi.org/10.5194/egusphere-2024-1390, https://doi.org/10.5194/egusphere-2024-1390, 2024
Short summary
Short summary
This study shows the derived organic aerosol hygroscopicity under high humidity conditions based on a simple optical scatter monitor system, including two nephelometric monitors (pDR-1500), after knowing the aerosol chemical composition.
Jiao Xue, Tian Zhang, Keyhong Park, Jinpei Yan, Young Jun Yoon, Jiyeon Park, and Bingbing Wang
Atmos. Chem. Phys., 24, 7731–7754, https://doi.org/10.5194/acp-24-7731-2024, https://doi.org/10.5194/acp-24-7731-2024, 2024
Short summary
Short summary
Ice formation by particles is an important way of making mixed-phase and ice clouds. We found that particles collected in the marine atmosphere exhibit diverse ice nucleation abilities and mixing states. Sea salt mixed-sulfate particles were enriched in ice-nucleating particles. Selective aging on sea salt particles made particle populations more externally mixed. Characterizations of particles and their mixing state are needed for a better understanding of aerosol–cloud interactions.
Yangzhi Mo, Jun Li, Guangcai Zhong, Sanyuan Zhu, Shizhen Zhao, Jiao Tang, Hongxing Jiang, Zhineng Cheng, Chongguo Tian, Yingjun Chen, and Gan Zhang
Atmos. Chem. Phys., 24, 7755–7772, https://doi.org/10.5194/acp-24-7755-2024, https://doi.org/10.5194/acp-24-7755-2024, 2024
Short summary
Short summary
In this study, we found that biomass burning (31.0 %) and coal combustion (31.1 %) were the dominant sources of water-insoluble organic carbon in China, with coal combustion sources exhibiting the strongest light-absorbing capacity. Additionally, we propose a light-absorbing carbonaceous continuum, revealing that components enriched with fossil sources tend to have stronger light-absorbing capacity, higher aromaticity, higher molecular weights, and greater recalcitrance in the atmosphere.
Jing Duan, Ru-Jin Huang, Ying Wang, Wei Xu, Haobin Zhong, Chunshui Lin, Wei Huang, Yifang Gu, Jurgita Ovadnevaite, Darius Ceburnis, and Colin O'Dowd
Atmos. Chem. Phys., 24, 7687–7698, https://doi.org/10.5194/acp-24-7687-2024, https://doi.org/10.5194/acp-24-7687-2024, 2024
Short summary
Short summary
The chemical composition of atmospheric particles has shown significant changes in recent years. We investigated the potential effects of changes in inorganics on aerosol water uptake and, thus, secondary organic aerosol formation in wintertime haze based on the size-resolved measurements of non-refractory fine particulate matter (NR-PM2.5) in Xi’an, northwestern China. We highlight the key role of aerosol water as a medium to link inorganics and organics in their multiphase processes.
Hongyong Li, Xiaopu Lyu, Likun Xue, Yunxi Huo, Dawen Yao, Haoxian Lu, and Hai Guo
Atmos. Chem. Phys., 24, 7085–7100, https://doi.org/10.5194/acp-24-7085-2024, https://doi.org/10.5194/acp-24-7085-2024, 2024
Short summary
Short summary
Organic aerosol is ubiquitous in the atmosphere and largely explains the gap between current levels of fine particulate matter in many cities and the World Health Organization guideline values. This study highlights the dominant contributions of cooking emissions to organic aerosol when marine air prevailed in Hong Kong, which were occasionally overwhelmed by aromatics-derived secondary organic aerosol in continental ouflows.
Shao Shi, Jinghao Zhai, Xin Yang, Yechun Ruan, Yuanlong Huang, Xujian Chen, Antai Zhang, Jianhuai Ye, Guomao Zheng, Baohua Cai, Yaling Zeng, Yixiang Wang, Chunbo Xing, Yujie Zhang, Tzung-May Fu, Lei Zhu, Huizhong Shen, and Chen Wang
Atmos. Chem. Phys., 24, 7001–7012, https://doi.org/10.5194/acp-24-7001-2024, https://doi.org/10.5194/acp-24-7001-2024, 2024
Short summary
Short summary
The determination of ions in the mass spectra of individual particles remains uncertain. We have developed a standard-free mass calibration algorithm applicable to more than 98 % of ambient particles. With our algorithm, ions with ~ 0.05 Th mass difference could be determined. Therefore, many more atmospheric species could be determined and involved in the source apportionment of aerosols, the study of chemical reaction mechanisms, and the analysis of single-particle mixing states.
Wei Sun, Xiaodong Hu, Yuzhen Fu, Guohua Zhang, Yujiao Zhu, Xinfeng Wang, Caiqing Yan, Likun Xue, He Meng, Bin Jiang, Yuhong Liao, Xinming Wang, Ping'an Peng, and Xinhui Bi
Atmos. Chem. Phys., 24, 6987–6999, https://doi.org/10.5194/acp-24-6987-2024, https://doi.org/10.5194/acp-24-6987-2024, 2024
Short summary
Short summary
The formation pathways of nitrogen-containing compounds (NOCs) in the atmosphere remain unclear. We investigated the composition of aerosols and fog water by state-of-the-art mass spectrometry and compared the formation pathways of NOCs. We found that NOCs in aerosols were mainly formed through nitration reaction, while ammonia addition played a more important role in fog water. The results deepen our understanding of the processes of organic particulate pollution.
Fuzhen Shen, Michaela I. Hegglin, and Yue Yuan
Atmos. Chem. Phys., 24, 6539–6553, https://doi.org/10.5194/acp-24-6539-2024, https://doi.org/10.5194/acp-24-6539-2024, 2024
Short summary
Short summary
We attempt to use a novel structural self-organising map and machine learning models to identify a weather system and quantify the importance of each meteorological factor in driving the unexpected PM2.5 and O3 changes under the specific weather system during the COVID-19 lockdown in China. The result highlights that temperature under the double-centre high-pressure system plays the most crucial role in abnormal events.
Wenshuai Li, Yuxuan Qi, Yingchen Liu, Guanru Wu, Yanjing Zhang, Jinhui Shi, Wenjun Qu, Lifang Sheng, Wencai Wang, Daizhou Zhang, and Yang Zhou
Atmos. Chem. Phys., 24, 6495–6508, https://doi.org/10.5194/acp-24-6495-2024, https://doi.org/10.5194/acp-24-6495-2024, 2024
Short summary
Short summary
Aerosol particles from mainland can transport to oceans and deposit, providing soluble Fe and affecting phytoplankton growth. Thus, we studied the dissolution process of aerosol Fe and found that photochemistry played a key role in promoting Fe dissolution in clean conditions. RH-dependent reactions were more influential in slightly polluted conditions. These results highlight the distinct roles of two weather-related parameters (radiation and RH) in influencing geochemical cycles related to Fe.
Yanqin Ren, Zhenhai Wu, Yuanyuan Ji, Fang Bi, Junling Li, Haijie Zhang, Hao Zhang, Hong Li, and Gehui Wang
Atmos. Chem. Phys., 24, 6525–6538, https://doi.org/10.5194/acp-24-6525-2024, https://doi.org/10.5194/acp-24-6525-2024, 2024
Short summary
Short summary
Nitrated aromatic compounds (NACs) and oxygenated derivatives of polycyclic aromatic hydrocarbons (OPAHs) in PM2.5 were examined from an urban area in Beijing during the autumn and winter. The OPAH and NAC concentrations were much higher during heating than before heating. They majorly originated from the combustion of biomass and automobile emissions, and the secondary generation was the major contributor throughout the whole sampling period.
Rime El Asmar, Zongrun Li, David J. Tanner, Yongtao Hu, Susan O’Neill, L. Gregory Huey, M. Talat Odman, and Rodney J. Weber
EGUsphere, https://doi.org/10.5194/egusphere-2024-1485, https://doi.org/10.5194/egusphere-2024-1485, 2024
Short summary
Short summary
Prescribed burning is an important method for managing ecosystems and preventing wildfires, however, smoke from prescribed fires can have a significant impact on air quality. Here, using a network of fixed sites and sampling throughout an extended prescribed burning period in two different years, we characterize the emissions and evolution up to 8 hours of PM2.5 mass, BC, and BrC in smoke from burning of forested lands in the southeastern US.
Gregory P. Schill, Karl D. Froyd, Daniel M. Murphy, Christina J. Williamson, Charles Brock, Tomás Sherwen, Mat J. Evans, Eric A. Ray, Eric C. Apel, Rebecca S. Hornbrook, Alan J. Hills, Jeff Peischl, Tomas B. Ryerson, Chelsea R. Thompson, Ilann Bourgeois, Donald R. Blake, Joshua P. DiGangi, and Glenn S. Diskin
EGUsphere, https://doi.org/10.5194/egusphere-2024-1399, https://doi.org/10.5194/egusphere-2024-1399, 2024
Short summary
Short summary
Using single-particle mass spectrometry, we show that trace concentrations of bromine and iodine are ubiquitous in remote tropospheric aerosol, and suggest that aerosols are an important part of the global reactive iodine budget. Comparisons to a global climate model with detailed iodine chemistry are favorable in the background atmosphere; however, the model cannot replicate our measurements near the ocean surface, in biomass burning plumes, and in the stratosphere.
Marco Paglione, David C. S. Beddows, Anna Jones, Thomas Lachlan-Cope, Matteo Rinaldi, Stefano Decesari, Francesco Manarini, Mara Russo, Karam Mansour, Roy M. Harrison, Andrea Mazzanti, Emilio Tagliavini, and Manuel Dall'Osto
Atmos. Chem. Phys., 24, 6305–6322, https://doi.org/10.5194/acp-24-6305-2024, https://doi.org/10.5194/acp-24-6305-2024, 2024
Short summary
Short summary
Applying factor analysis techniques to H-NMR spectra, we present the organic aerosol (OA) source apportionment of PM1 samples collected in parallel at two Antarctic stations, namely Signy and Halley, allowing investigation of aerosol–climate interactions in an unperturbed atmosphere. Our results show remarkable differences between pelagic (open-ocean) and sympagic (sea-ice-influenced) air masses and indicate that various sources and processes are controlling Antarctic aerosols.
Zhichao Dong, Chandra Mouli Pavuluri, Peisen Li, Zhanjie Xu, Junjun Deng, Xueyan Zhao, Xiaomai Zhao, Pingqing Fu, and Cong-Qiang Liu
Atmos. Chem. Phys., 24, 5887–5905, https://doi.org/10.5194/acp-24-5887-2024, https://doi.org/10.5194/acp-24-5887-2024, 2024
Short summary
Short summary
Comprehensive study of optical properties of brown carbon (BrC) in fine aerosols from Tianjin, China, implied that biological emissions are major sources of BrC in summer, whereas fossil fuel combustion and biomass burning emissions are in cold periods. The direct radiation absorption caused by BrC in short wavelengths contributed about 40 % to that caused by BrC in 300–700 nm. Water-insoluble but methanol-soluble BrC contains more protein-like chromophores (PLOM) than that of water-soluble BrC.
Kumiko Goto-Azuma, Yoshimi Ogawa-Tsukagawa, Kaori Fukuda, Koji Fujita, Motohiro Hirabayashi, Remi Dallmayr, Jun Ogata, Nobuhiro Moteki, Tatsuhiro Mori, Sho Ohata, Yutaka Kondo, Makoto Koike, Sumito Matoba, and Teruo Aoki
EGUsphere, https://doi.org/10.5194/egusphere-2024-1498, https://doi.org/10.5194/egusphere-2024-1498, 2024
Short summary
Short summary
Monthly records spanning 350 years from a Greenland ice core reveal trends in black carbon (BC) concentrations and sizes. BC concentrations have risen since the late 19th century due to the inflow of anthropogenic BC, with these particles being larger than those from biomass burning (BB). High BB BC concentration peaks in summer originating from BB could reduce albedo. However, BB BC showed no upward trend until the early 2000s. Our findings are crucial for validating aerosol and climate models.
Shan Wang, Kezheng Liao, Zijing Zhang, Yuk Ying Cheng, Qiongqiong Wang, Hanzhe Chen, and Jian Zhen Yu
Atmos. Chem. Phys., 24, 5803–5821, https://doi.org/10.5194/acp-24-5803-2024, https://doi.org/10.5194/acp-24-5803-2024, 2024
Short summary
Short summary
In this work, hourly primary and secondary organic carbon were estimated by a novel Bayesian inference approach in suburban Hong Kong. Their multi-temporal-scale variations and evolution characteristics during PM2.5 episodes were examined. The methodology could serve as a guide for other locations with similar monitoring capabilities. The observation-based results are helpful for understanding the evolving nature of secondary organic aerosols and refining the accuracy of model simulations.
Andreas Aktypis, Dontavious Sippial, Christina Vasilakopoulou, Angeliki Matrali, Christos Kaltsonoudis, Andrea Simonati, Marco Paglione, Matteo Rinaldi, Stefano Decesari, and Spyros Pandis
EGUsphere, https://doi.org/10.5194/egusphere-2024-1317, https://doi.org/10.5194/egusphere-2024-1317, 2024
Short summary
Short summary
A dual chamber system was deployed in two different environments (Po Valley, Italy and Pertouli forest, Greece) to study the potential of ambient air directly injected into the chambers, to form secondary aerosol. In the Po Valley, the system reacts rapidly forming large amounts of SOA, while in Pertouli the corresponding SOA formation chemistry appears to have been practically terminated before the beginning of most experiments, so there is little additional SOA formation potential left.
Mingfu Cai, Chenshuo Ye, Bin Yuan, Shan Huang, E Zheng, Suxia Yang, Zelong Wang, Yi Lin, Tiange Li, Weiwei Hu, Wei Chen, Qicong Song, Wei Li, Yuwen Peng, Baolin Liang, Qibin Sun, Jun Zhao, Duohong Chen, Jiaren Sun, Zhiyong Yang, and Min Shao
EGUsphere, https://doi.org/10.5194/egusphere-2024-887, https://doi.org/10.5194/egusphere-2024-887, 2024
Short summary
Short summary
This study investigated the daytime secondary organic aerosol (SOA) formation in urban plumes. We observed a significant daytime SOA formation through gas-particle partitioning when the site was affected by urban plumes. Box model simulation indicated that urban pollutants (nitrogen oxide and volatile organic compounds) could enhance the oxidizing capacity, while the elevated volatile organic compounds were mainly responsible for promoting daytime SOA formation.
James Brean, David C. S. Beddows, Eija Asmi, Ari Virkkula, Lauriane L. J. Quéléver, Mikko Sipilä, Floortje Van Den Heuvel, Thomas Lachlan-Cope, Anna Jones, Markus Frey, Angelo Lupi, Jiyeon Park, Young Jun Yoon, Ralf Weller, Giselle L. Marincovich, Gabriela C. Mulena, Roy M. Harrison, and Manuel Dall´Osto
EGUsphere, https://doi.org/10.5194/egusphere-2024-987, https://doi.org/10.5194/egusphere-2024-987, 2024
Short summary
Short summary
Our results emphasize how understanding the geographical variation in surface types across the Antarctic is key to understanding secondary aerosol sources.
Qun He, Zhaowen Wang, Houfeng Liu, Pengju Xu, Rongbao Duan, Caihong Xu, Jianmin Chen, and Min Wei
EGUsphere, https://doi.org/10.5194/egusphere-2024-841, https://doi.org/10.5194/egusphere-2024-841, 2024
Short summary
Short summary
Coastal environments provide an ideal setting for investigating the intermixing processes of terrestrial and marine aerosols. Terrestrial air mass constituted a larger proportion during severe air pollution, harboring more animal and human pathogens. A relative shift towards marine air-mass with respect to pollution elimination, where saprophytic bacteria and fungi were predominant. Mixed air-mass reveals the intermixing processes of terrestrial and marine sources.
Cited articles
Alfarra, M. R., Paulsen, D., Gysel, M., Garforth, A. A., Dommen, J.,
Prévôt, A. S. H., Worsnop, D. R., Baltensperger, U., and Coe, H.: A
mass spectrometric study of secondary organic aerosols formed from the
photooxidation of anthropogenic and biogenic precursors in a reaction
chamber, Atmos. Chem. Phys., 6, 5279–5293,
https://doi.org/10.5194/acp-6-5279-2006, 2006.
Alvarez-Aviles, L., Simpson, W. R., Douglas, T. A., Sturm, M., Perovich, D.,
and Domine, F.: Frost flower chemical composition during growth and its
implications for aerosol production and bromine activation, J. Geophys.
Res.-Atmos., 113, D21304, https://doi.org/10.1029/2008jd010277, 2008.
Alves, C. A. and Pio, C. A.: Secondary organic compounds in atmospheric
aerosols: Speciation and formation mechanisms, J. Brazil. Chem. Soc., 16,
1017–1029, https://doi.org/10.1590/s0103-50532005000600020, 2005.
Arrigo, K. R., van Dijken, G. L., and Bushinsky, S.: Primary production in
the Southern Ocean, 1997–2006, J. Geophys. Res.-Oceans, 113, C08004,
https://doi.org/10.1029/2007jc004551, 2008.
Asmi, E., Frey, A., Virkkula, A., Ehn, M., Manninen, H. E., Timonen, H.,
Tolonen-Kivimäki, O., Aurela, M., Hillamo, R., and Kulmala, M.:
Hygroscopicity and chemical composition of Antarctic sub-micrometre aerosol
particles and observations of new particle formation, Atmos. Chem. Phys., 10,
4253–4271, https://doi.org/10.5194/acp-10-4253-2010, 2010.
Asmi, E., Neitola, K., Teinila, K., Rodriguez, E., Virkkula, A., Backman, J.,
Bloss, M., Jokela, J., Lihavainen, H., De Leeuw, G., Paatero, J., Aaltonen,
V., Mei, M., Gambarte, G., Copes, G., Albertini, M., Fogwill, G. P., Ferrara,
J., Barlasina, M. E., and Sanchez, R.: Primary sources control the
variability of aerosol optical properties in the Antarctic Peninsula, Tellus
B, 70, 1, https://doi.org/10.1080/16000889.2017.1414571, 2018.
Attwood, A. R., Washenfelder, R. A., Brock, C. A., Hu, W., Baumann, K.,
Campuzano-Jost, P., Day, D. A., Edgerton, E. S., Murphy, D. M., Palm, B. B.,
McComiskey, A., Wagner, N. L., de Sa, S. S., Ortega, A., Martin, S. T.,
Jimenez, J. L., and Brown, S. S.: Trends in sulfate and organic aerosol mass
in the Southeast U.S.: Impact on aerosol optical depth and radiative forcing,
Geophys. Res. Lett., 41, 7701–7709, 10.1002/2014gl061669, 2014.
Barbaro, E., Kirchgeorg, T., Zangrando, R., Vecchiato, M., Piazza, R.,
Barbante, C., and Garnbaro, A.: Sugars in Antarctic aerosol, Atmos. Environ.,
118, 135–144, https://doi.org/10.1016/j.atmosenv.2015.07.047, 2015a.
Barbaro, E., Zangrando, R., Vecchiato, M., Piazza, R., Cairns, W. R. L.,
Capodaglio, G., Barbante, C., and Gambaro, A.: Free amino acids in Antarctic
aerosol: potential markers for the evolution and fate of marine aerosol,
Atmos. Chem. Phys., 15, 5457–5469, https://doi.org/10.5194/acp-15-5457-2015,
2015b.
Barbaro, E., Zangrando, R., Kirchgeorg, T., Bazzano, A., Illuminati, S.,
Annibaldi, A., Rella, S., Truzzi, C., Grotti, M., Ceccarini, A., Malitesta,
C., Scarponi, G., and Gambaro, A.: An integrated study of the chemical
composition of Antarctic aerosol to investigate natural and anthropogenic
sources, Environ. Chem., 13, 867–876, 10.1071/en16056, 2016.
Barbaro, E., Padoan, S., Kirchgeorg, T., Zangrando, R., Toscano, G.,
Barbante, C., and Gambaro, A.: Particle size distribution of inorganic and
organic ions in coastal and inland Antarctic aerosol, Environ. Sci. Pollut.
R., 24, 2724–2733, https://doi.org/10.1007/s11356-016-8042-x, 2017.
Beaton, A. E. and Tukey, J. W.: The Fitting of Power Series, Meaning
Polynomials, Illustrated on Band-Spectroscopic Data, Technometrics, 16,
147–185, https://doi.org/10.2307/1267936, 1974.
Bintanja, R., Severijns, C., Haarsma, R., and Hazeleger, W.: The future of
Antarctica's surface winds simulated by a high-resolution global climate
model: 1. Model description and validation, J. Geophys. Res.-Atmos., 119,
7136–7159, https://doi.org/10.1002/2013jd020847, 2014.
Bodhaine, B. A.: Aerosol measurements at four background sites, J. Geophys.
Res.-Oceans, 88, 10753–10768, 1983.
Bodhaine, B. A., Deluisi, J. J., Harris, J. M., Houmere, P., and Bauman, S.:
Aerosol measurements at the South Pole, Tellus B, 38, 223–235, 1986.
Bromwich, D. H., Nicolas, J. P., Monaghan, A. J., Lazzara, M. A., Keller, L.
M., Weidner, G. A., and Wilson, A. B.: Central West Antarctica among the most
rapidly warming regions on Earth, Nat. Geosci., 6, 139–145,
https://doi.org/10.1038/ngeo1671, 2013.
Cadle, R. D., Fischer, W. H., Frank, E. R., and Lodge, J. P.: Particles in
Antarctic Atmosphere, J. Atmos. Sci., 25, 100–103,
https://doi.org/10.1175/1520-0469(1968)025<0100:pitaa>2.0.co;2, 1968.
Charbouillot, T., Gorini, S., Voyard, G., Parazols, M., Brigante, M.,
Deguillaume, L., Delort, A. M., and Mailhot, G.: Mechanism of carboxylic acid
photooxidation in atmospheric aqueous phase: Formation, fate and reactivity,
Atmos. Environ., 56, 1–8, https://doi.org/10.1016/j.atmosenv.2012.03.079, 2012.
Cheung, K. L., Ntziachristos, L., Tzamkiozis, T., Schauer, J. J., Samaras,
Z., Moore, K. F., and Sioutas, C.: Emissions of Particulate Trace Elements,
Metals and Organic Species from Gasoline, Diesel, and Biodiesel Passenger
Vehicles and Their Relation to Oxidative Potential, Aerosol Sci. Tech., 44,
500–513, https://doi.org/10.1080/02786821003758294, 2010.
Claeys, M., Szmigielski, R., Kourtchev, I., Van der Veken, P., Vermeylen, R.,
Maenhaut, W., Jaoui, M., Kleindienst, T. E., Lewandowski, M., and Offenberg,
J. H.: Hydroxydicarboxylic acids: markers for secondary organic aerosol from
the photooxidation of α-pinene, Environ. Sci. Technol., 41,
1628–1634, 2007.
Cowie, G. L. and Hedges, J. I.: Sources and reactivities of amino acids in a
coastal marine environment, Limnol. Oceanogr., 37, 703–724,
https://doi.org/10.4319/lo.1992.37.4.0703, 1992.
Croft, B., Martin, R. V., Leaitch, W. R., Tunved, P., Breider, T. J.,
D'Andrea, S. D., and Pierce, J. R.: Processes controlling the annual cycle of
Arctic aerosol number and size distributions, Atmos. Chem. Phys., 16,
3665–3682, https://doi.org/10.5194/acp-16-3665-2016, 2016a.
Croft, B., Wentworth, G. R., Martin, R. V., Leaitch, W. R., Murphy, J. G.,
Murphy, B. N., Kodros, J. K., Abbatt, J. P. D., and Pierce, J. R.:
Contribution of Arctic seabird-colony ammonia to atmospheric particles and
cloud-albedo radiative effect, Nat. Commun., 7, 13444,
https://doi.org/10.1038/ncomms13444, 2016b.
Dall'Osto, M., Ceburnis, D., Monahan, C., Worsnop, D. R., Bialek, J.,
Kulmala, M., Kurten, T., Ehn, M., Wenger, J., Sodeau, J., Healy, R., and
O'Dowd, C.: Nitrogenated and aliphatic organic vapors as possible drivers for
marine secondary organic aerosol growth, J. Geophys. Res.-Atmos., 117,
D12311, https://doi.org/10.1029/2012jd017522, 2012.
Dall'Osto, M., Ovadnevaite, J., Paglione, M., Beddows, D. C. S., Ceburnis,
D., Cree, C., Cortes, P., Zamanillo, M., Nunes, S. O., Perez, G. L.,
Ortega-Retuerta, E., Emelianov, M., Vaque, D., Marrase, C., Estrada, M.,
Sala, M. M., Vidal, M., Fitzsimons, M. F., Beale, R., Airs, R., Rinaldi, M.,
Decesari, S., Facchini, M. C., Harrison, R. M., O'Dowd, C., and Simo, R.:
Antarctic sea ice region as a source of biogenic organic nitrogen in
aerosols, Scientific Reports, 7, 6047, https://doi.org/10.1038/s41598-017-06188-x, 2017.
Davis, L. S., Harcourt, R. G., and Bradshaw, C. J. A.: The winter migration
of Adelie penguins breeding in the Ross Sea sector of Antarctica, Polar
Biol., 24, 593–597, https://doi.org/10.1007/s003000100256, 2001.
Defelice, T. P., Saxena, V. K., and Yu, S. C.: On the measurements of cloud
condensation nuclei at Palmer Station, Antarctica, Atmos. Environ., 31,
4039–4044, https://doi.org/10.1016/s1352-2310(97)00250-1, 1997.
Domine, F., Sparapani, R., Ianniello, A., and Beine, H. J.: The origin of sea
salt in snow on Arctic sea ice and in coastal regions, Atmos. Chem. Phys., 4,
2259–2271, https://doi.org/10.5194/acp-4-2259-2004, 2004.
Draxier, R. R. and Hess, G. D.: An overview of the HYSPLIT_4 modelling
system for trajectories, dispersion and deposition, Aust. Meteorol. Mag., 47,
295–308, 1998.
Frossard, A. A., Shaw, P. M., Russell, L. M., Kroll, J. H., Canagaratna, M.
R., Worsnop, D. R., Quinn, P. K., and Bates, T. S.: Springtime Arctic haze
contributions of submicron organic particles from European and Asian
combustion sources, J. Geophys. Res.-Atmos., 116, D05205,
https://doi.org/10.1029/2010jd015178, 2011.
Frossard, A. A., Russell, L. M., Keene, W. C., Kieber, D. J., Quinn, P. K.,
and Bates, T. S.: Regional Signatures in the Organic Composition of Marine
Aerosol Particles, in: AIP Conference Proceedings, 19th International
Conference on Nucleation and Atmospheric Aerosols (ICNAA), Colorado State
Univ, Ctr Arts, Fort Collins, CO, 2013, 543–546, 2013.
Frossard, A. A., Russell, L. M., Burrows, S. M., Elliott, S. M., Bates, T.
S., and Quinn, P. K.: Sources and composition of submicron organic mass in
marine aerosol particles, J. Geophys. Res.-Atmos., 119, 12977–13003,
https://doi.org/10.1002/2014jd021913, 2014a.
Frossard, A. A., Russell, L. M., Massoli, P., Bates, T. S., and Quinn, P. K.:
Side-by-Side Comparison of Four Techniques Explains the Apparent Differences
in the Organic Composition of Generated and Ambient Marine Aerosol Particles,
Aerosol Sci. Tech., 48, V–X, https://doi.org/10.1080/02786826.2013.879979, 2014b.
Gagosian, R. B. and Stuermer, D. H.: The cycling of biogenic compounds and
their diagenetically transformed products in seawater, Mar. Chem., 5,
605–632, 1977.
Giordano, M. R., Kalnajs, L. E., Avery, A., Goetz, J. D., Davis, S. M., and
DeCarlo, P. F.: A missing source of aerosols in Antarctica – beyond
long-range transport, phytoplankton, and photochemistry, Atmos. Chem. Phys.,
17, 1–20, https://doi.org/10.5194/acp-17-1-2017, 2017.
Gordon, M. and Taylor, P. A.: Measurements of blowing snow, Part I: Particle
shape, size distribution, velocity, and number flux at Churchill, Manitoba,
Canada, Cold Reg. Sci. Technol., 55, 63–74,
https://doi.org/10.1016/j.coldregions.2008.05.001, 2009.
Goring, D. G. and Nikora, V. I.: Despiking acoustic Doppler velocimeter data,
J. Hydraul. Eng.-ASCE, 128, 117–126,
https://doi.org/10.1061/(asce)0733-9429(2002)128:1(117), 2002.
Gras, J. L.: Condensation nucleus size distribution at Mawson, Antarctica –
microphysics and chemistry, Atmos. Environ. A-Gen., 27, 1427–1434,
https://doi.org/10.1016/0960-1686(93)90128-l, 1993.
Guzman-Morales, J., Frossard, A. A., Corrigan, A. L., Russell, L. M., Liu,
S., Takahama, S., Taylor, J. W., Allan, J., Coe, H., Zhao, Y., and Goldstein,
A. H.: Estimated contributions of primary and secondary organic aerosol from
fossil fuel combustion during the CalNex and Cal-Mex campaigns, Atmos.
Environ., 88, 330–340, 10.1016/j.atmosenv.2013.08.047, 2014.
Hansen, A. D. A., Bodhaine, B. A., Dutton, E. G., and Schnell, R. C.: Aerosol
Black Carbon Measurements at the South-Pole – Initial Results, 1986–1987,
Geophys. Res. Lett., 15, 1193–1196, https://doi.org/10.1029/GL015i011p01193, 1988.
Hansen, A. D. A., Lowenthal, D. H., Chow, J. C., and Watson, J. G.: Black
carbon aerosol at McMurdo station, Antarctica, J. Air Waste Manage., 51,
593–600, 2001.
Hara, K., Osada, K., Kido, M., Hayashi, M., Matsunaga, K., Iwasaka, Y.,
Yamanouchi, T., Hashida, G., and Fukatsu, T.: Chemistry of sea-salt particles
and inorganic halogen species in Antarctic regions: Compositional differences
between coastal and inland stations, J. Geophys. Res.-Atmos., 109, D20208,
https://doi.org/10.1029/2004JD004713, 2004.
Hara, K., Osada, K., Kido, M., Matsunaga, K., Iwasaka, Y., Hashida, G., and
Yamanouchi, T.: Variations of constituents of individual sea-salt particles
at Syowa station, Antarctica, Tellus B, 57, 230–246,
https://doi.org/10.1111/j.1600-0889.2005.00142.x, 2005.
Hara, K., Osada, K., Yabuki, M., Hashida, G., Yamanouchi, T., Hayashi, M.,
Shiobara, M., Nishita, C., and Wada, M.: Haze episodes at Syowa Station,
coastal Antarctica: Where did they come from?, J. Geophys. Res.-Atmos., 115,
D14205, https://doi.org/10.1029/2009JD012582, 2010.
Harder, S., Warren, S. G., and Charlson, R. J.: Sulfate in air and snow at
the South Pole: Implications for transport and deposition at sites with low
snow accumulation, J. Geophys. Res.-Atmos., 105, 22825–22832, 2000.
Hartigan, J. A. and Wong, M. A.: Algorithm AS 136: A k-means clustering
algorithm, J. Roy. Stat. Soc. C-App., 28, 100–108, 1979.
Hawkins, L. N. and Russell, L.: Polysaccharides, Proteins, and Phytoplankton
Fragments: Four Chemically Distinct Types of Marine Primary Organic Aerosol
Classified by Single Particle Spectromicroscopy, Adv. Meteorol., 14, 612132,
https://doi.org/10.1155/2010/612132, 2010.
Hofmann, D.: Balloon-borne measurements of middle atmosphere aerosols and
trace gases in Antarctica, Rev. Geophy., 26, 113–130, 1988.
Hofmann, D. J., Rosen, J. M., Harder, J. A., and Rolf, S. R.: Ozone and
aerosol measurements in the springtime Antarctic Stratosphere in 1985,
Geophys. Res. Lett., 13, 1252–1255, https://doi.org/10.1029/GL013i012p01252, 1986.
Hogan, A. W.: Antarctic aerosols, J. Appl. Meteorol., 14, 550–559,
https://doi.org/10.1175/1520-0450(1975)014<0550:aa>2.0.co;2, 1975.
Hogan, A. W. and Barnard, S.: Seasonal and frontal variation in Antarctic
aerosol concentrations, J. Appl. Meteorol., 17, 1458–1465,
https://doi.org/10.1175/1520-0450(1978)017<1458:safvia>2.0.co;2, 1978.
Holland, P. R.: The seasonality of Antarctic sea ice trends, Geophys. Res.
Lett., 41, 4230–4237, https://doi.org/10.1002/2014gl060172, 2014.
Huang, J. and Jaeglé, L.: Wintertime enhancements of sea salt aerosol in
polar regions consistent with a sea ice source from blowing snow, Atmos.
Chem. Phys., 17, 3699–3712, https://doi.org/10.5194/acp-17-3699-2017, 2017.
IPCC: Summary for policymakers in climate change 2013: the physical science
basis, contribution of working group I to the fifth assessment report of the
intergovernmental panel on climate change, edited by: Stocker, T. F., Qin,
D., Plattner, G. K., Tignor, M., Allen, S. K., Boschung, J., Nauels, A., Xia,
Y., Bex, V., and Midgley, P. M., Cambridge Univ Press, Cambridge, UK and New
York, 2013.
Jourdain, B. and Legrand, M.: Year-round records of bulk and size-segregated
aerosol composition and HCl and HNO3 levels in the Dumont d'Urville
(coastal Antarctica) atmosphere: Implications for sea-salt aerosol
fractionation in the winter and summer, J. Geophys. Res.-Atmos., 107, 4645,
https://doi.org/10.1029/2002jd002471, 2002.
Jourdain, B., Preunkert, S., Cerri, O., Castebrunet, H., Udisti, R., and
Legrand, M.: Year-round record of size-segregated aerosol composition in
central Antarctica (Concordia station): Implications for the degree of
fractionation of sea-salt particles, J. Geophys. Res.-Atmos., 113, D14308,
https://doi.org/10.1029/2007jd009584, 2008.
Kalnajs, L. E., Avallone, L. M., and Toohey, D. W.: Correlated measurements
of ozone and particulates in the Ross Island region, Antarctica, Geophys.
Res. Lett., 40, 6319–6323, 10.1002/2013gl058422, 2013.
Kawamura, K. and Gagosian, R. B.: Implications of omega-oxocarboxylic acids
in the remote marine atmosphere for photooxidation of unsaturated fatty
acids, Nature, 325, 330–332, https://doi.org/10.1038/325330a0, 1987.
Khan, A. L., McMeeking, G. R., Schwarz, J. P., Xian, P., Welch, K. A., Berry
Lyons, W., and McKnight, D. M.: Near-Surface Refractory Black Carbon
Observations in the Atmosphere and Snow in the McMurdo Dry Valleys,
Antarctica, and Potential Impacts of Foehn Winds, J. Geophys. Res.-Atmos.,
123, 2877–2887, 2018.
Kim, J., Yoon, Y. J., Gim, Y., Kang, H. J., Choi, J. H., Park, K.-T., and
Lee, B. Y.: Seasonal variations in physical characteristics of aerosol
particles at the King Sejong Station, Antarctic Peninsula, Atmos. Chem.
Phys., 17, 12985–12999, https://doi.org/10.5194/acp-17-12985-2017, 2017.
Korhonen, H., Carslaw, K. S., Spracklen, D. V., Mann, G. W., and Woodhouse,
M. T.: Influence of oceanic dimethyl sulfide emissions on cloud condensation
nuclei concentrations and seasonality over the remote Southern Hemisphere
oceans: A global model study, J. Geophys. Res.-Atmos., 113, D15204,
https://doi.org/10.1029/2007jd009718, 2008.
Kuznetsova, M., Lee, C., and Aller, J.: Characterization of the proteinaceous
matter in marine aerosols, Mar. Chem., 96, 359–377,
https://doi.org/10.1016/j.marchem.2005.03.007, 2005.
Kyrö, E.-M., Kerminen, V.-M., Virkkula, A., Dal Maso, M., Parshintsev,
J., Ruíz-Jimenez, J., Forsström, L., Manninen, H. E., Riekkola,
M.-L., Heinonen, P., and Kulmala, M.: Antarctic new particle formation from
continental biogenic precursors, Atmos. Chem. Phys., 13, 3527–3546,
https://doi.org/10.5194/acp-13-3527-2013, 2013.
Lambeck, K., Esat, T. M., and Potter, E. K.: Links between climate and sea
levels for the past three million years, Nature, 419, 199–206,
https://doi.org/10.1038/nature01089, 2002.
Leaitch, W. R., Russell, L. M., Liu, J., Kolonjari, F., Toom, D., Huang, L.,
Sharma, S., Chivulescu, A., Veber, D., and Zhang, W.: Organic functional
groups in the submicron aerosol at 82.5∘ N, 62.5∘ W from
2012 to 2014, Atmos. Chem. Phys., 18, 3269–3287,
https://doi.org/10.5194/acp-18-3269-2018, 2018.
Legrand, M., Ducroz, F., Wagenbach, D., Mulvaney, R., and Hall, J.: Ammonium
in coastal Antarctic aerosol and snow: Role of polar ocean and penguin
emissions, J. Geophys. Res.-Atmos., 103, 11043–11056, https://doi.org/10.1029/97jd01976,
1998.
Legrand, M., Gros, V., Preunkert, S., Sarda-Esteve, R., Thierry, A. M., Pepy,
G., and Jourdain, B.: A reassessment of the budget of formic and acetic acids
in the boundary layer at Dumont d'Urville (coastal Antarctica): The role of
penguin emissions on the budget of several oxygenated volatile organic
compounds, J. Geophys. Res.-Atmos., 117, D06308, https://doi.org/10.1029/2011jd017102,
2012.
Legrand, M., Preunkert, S., Weller, R., Zipf, L., Elsässer, C., Merchel,
S., Rugel, G., and Wagenbach, D.: Year-round record of bulk and
size-segregated aerosol composition in central Antarctica (Concordia site) –
Part 2: Biogenic sulfur (sulfate and methanesulfonate) aerosol, Atmos. Chem.
Phys., 17, 14055–14073, https://doi.org/10.5194/acp-17-14055-2017, 2017a.
Legrand, M., Preunkert, S., Wolff, E., Weller, R., Jourdain, B., and
Wagenbach, D.: Year-round records of bulk and size-segregated aerosol
composition in central Antarctica (Concordia site) – Part 1: Fractionation
of sea-salt particles, Atmos. Chem. Phys., 17, 14039–14054,
https://doi.org/10.5194/acp-17-14039-2017, 2017b.
Lin, Y.-C., Tsai, C.-J., Wu, Y.-C., Zhang, R., Chi, K.-H., Huang, Y.-T., Lin,
S.-H., and Hsu, S.-C.: Characteristics of trace metals in traffic-derived
particles in Hsuehshan Tunnel, Taiwan: size distribution, potential source,
and fingerprinting metal ratio, Atmos. Chem. Phys., 15, 4117–4130,
https://doi.org/10.5194/acp-15-4117-2015, 2015.
Liu, J., Lewis, S., and Russell, L. M.: Organic and Elemental Composition of
Submicron Aerosol Particles during AWARE at McMurdo Station, Antarctica,
https://doi.org/10.6075/J0WM1BKV, 2018.
Loureiro, A., Vasconcellos, M., and Pereira, E.: Trace element determination
in aerosols from the Antarctic Peninsula by neutron activation analysis, J.
Radioanal. Nucl. Ch., 159, 21–28, 1992.
Lyver, P. O., Barron, M., Barton, K. J., Ainley, D. G., Pollard, A., Gordon,
S., McNeill, S., Ballard, G., and Wilson, P. R.: Trends in the Breeding
Population of Adelie Penguins in the Ross Sea, 1981–2012: A Coincidence of
Climate and Resource Extraction Effects, Plos One, 9,
https://doi.org/10.1371/journal.pone.0091188, 2014.
Mace, K. A., Duce, R. A., and Tindale, N. W.: Organic nitrogen in rain and
aerosol at Cape Grim, Tasmania, Australia, J. Geophys. Res.-Atmos., 108,
4338, https://doi.org/10.1029/2002jd003051, 2003a.
Mace, K. A., Kubilay, N., and Duce, R. A.: Organic nitrogen in rain and
aerosol in the eastern Mediterranean atmosphere: An association with
atmospheric dust, J. Geophys. Res.-Atmos., 108, 4320,
https://doi.org/10.1029/2002jd002997, 2003b.
Mandalakis, M., Apostolaki, M., Tziaras, T., Polymenakou, P., and Stephanou,
E. G.: Free and combined amino acids in marine background atmospheric
aerosols over the Eastern Mediterranean, Atmos. Environ., 45, 1003–1009,
https://doi.org/10.1016/j.atmosenv.2010.10.046, 2011.
Maria, S. F., Russell, L. M., Turpin, B. J., and Porcja, R. J.: FTIR
measurements of functional groups and organic mass in aerosol samples over
the Caribbean, Atmos. Environ., 36, 5185–5196,
https://doi.org/10.1016/s1352-2310(02)00654-4, 2002.
Matsumoto, K. and Uematsu, M.: Free amino acids in marine aerosols over the
western North Pacific Ocean, Atmos. Environ., 39, 2163–2170,
https://doi.org/10.1016/j.atmosenv.2004.12.022, 2005.
Mazzera, D. M., Lowenthal, D. H., Chow, J. C., and Watson, J. G.: Sources of
PM10 and sulfate aerosol at McMurdo station, Antarctica, Chemosphere,
45, 347–356, https://doi.org/10.1016/s0045-6535(00)00591-9, 2001a.
Mazzera, D. M., Lowenthal, D. H., Chow, J. C., Watson, J. G., and Grubisic,
V.: PM10 measurements at McMurdo Station, Antarctica, Atmos. Environ.,
35, 1891–1902, https://doi.org/10.1016/s1352-2310(00)00409-x, 2001b.
McCoy, D. T., Burrows, S. M., Wood, R., Grosvenor, D. P., Elliott, S. M., Ma,
P.-L., Rasch, P. J., and Hartmann, D. L.: Natural aerosols explain seasonal
and spatial patterns of Southern Ocean cloud albedo, Sci. Adv., 1, e1500157,
https://doi.org/10.1126/sciadv.1500157, 2015.
McNeill, V. F.: Aqueous Organic Chemistry in the Atmosphere: Sources and
Chemical Processing of Organic Aerosols, Environ. Sci. Technol., 49,
1237–1244, https://doi.org/10.1021/es5043707, 2015.
Milne, P. J. and Zika, R. G.: Amino-acid nitrogen in atmospheric aerosols –
occurrence, sources and photochemical modification, J. Atmos. Chem., 16,
361–398, https://doi.org/10.1007/bf01032631, 1993.
Minikin, A., Legrand, M., Hall, J., Wagenbach, D., Kleefeld, C., Wolff, E.,
Pasteur, E. C., and Ducroz, F.: Sulfur-containing species (sulfate and
methanesulfonate) in coastal Antarctic aerosol and precipitation, J. Geophys.
Res.-Atmos. 103, 10975–10990, 1998.
Mishra, V. K., Kim, K.-H., Hong, S., and Lee, K.: Aerosol composition and its
sources at the King Sejong Station, Antarctic peninsula, Atmos. Environ., 38,
4069–4084, 2004.
Modini, R. L., Frossard, A. A., Ahlm, L., Russell, L. M., Corrigan, C. E.,
Roberts, G. C., Hawkins, L. N., Schroder, J. C., Bertram, A. K., Zhao, R.,
Lee, A. K. Y., Abbatt, J. P. D., Lin, J., Nenes, A., Wang, Z., Wonaschutz,
A., Sorooshian, A., Noone, K. J., Jonsson, H., Seinfeld, J. H., Toom-Sauntry,
D., Macdonald, A. M., and Leaitch, W. R.: Primary marine aerosol-cloud
interactions off the coast of California, J. Geophys. Res.-Atmos., 120,
4282–4303, https://doi.org/10.1002/2014jd022963, 2015.
Olson, M. R., Garcia, M. V., Robinson, M. A., Van Rooy, P., Dietenberger, M.
A., Bergin, M., and Schauer, J. J.: Investigation of black and brown carbon
multiple-wavelength-dependent light absorption from biomass and fossil fuel
combustion source emissions, J. Geophys. Res.-Atmos., 120, 6682–6697,
https://doi.org/10.1002/2014jd022970, 2015.
Ondov, J. M., Gladney, E. S., Zoller, W. H., Duce, R. A., and Jones, A. G.:
Atmospheric particulates at South-Pole station, Antarct. J. US, 8, 182–183,
1973a.
Ondov, J. M., Gladney, E. S., Zoller, W. H., Duce, R. A., and Jones, A. G.:
Atmospheric particulates at South-Pole station, Antarct. J. US, 8, 182–183,
1973b.
Paatero, P.: Least squares formulation of robust non-negative factor
analysis, Chemometr. Intell. Lab., 37, 23–35,
https://doi.org/10.1016/s0169-7439(96)00044-5, 1997.
Paatero, P. and Tapper, U.: Positive Matrix Factorization: A Non-Negative
Factor Model with Optimal Utilization of Error Estimates of Data Values,
Environmetrics, 5, 111–126, https://doi.org/10.1002/env.3170050203, 1994.
Parungo, F., Bodhaine, B., and Bortniak, J.: Seasonal variation in Antarctic
aerosol, J. Aerosol Sci., 12, 491–504, https://doi.org/10.1016/0021-8502(81)90052-5,
1981.
Peng, J., Hu, M., Guo, S., Du, Z., Shang, D., Zheng, J., Zheng, J., Zeng, L.,
Shao, M., Wu, Y., Collins, D., and Zhang, R.: Ageing and hygroscopicity
variation of black carbon particles in Beijing measured by a
quasi-atmospheric aerosol evolution study (QUALITY) chamber, Atmos. Chem.
Phys., 17, 10333–10348, https://doi.org/10.5194/acp-17-10333-2017, 2017.
Petters, M. D. and Kreidenweis, S. M.: A single parameter representation of
hygroscopic growth and cloud condensation nucleus activity, Atmos. Chem.
Phys., 7, 1961–1971, https://doi.org/10.5194/acp-7-1961-2007, 2007.
Polissar, A. V., Hopke, P. K., Paatero, P., Kaufmann, Y. J., Hall, D. K.,
Bodhaine, B. A., Dutton, E. G., and Harris, J. M.: The aerosol at Barrow,
Alaska: long-term trends and source locations, Atmos. Environ., 33,
2441–2458, https://doi.org/10.1016/s1352-2310(98)00423-3, 1999.
Price, D. J., Chen, C.-L., Russell, L. M., Lamjiri, M. A., Betha, R.,
Sanchez, K., Liu, J., Lee, A. K. Y., and Cocker, D. R.: More unsaturated,
cooking-type hydrocarbon-like organic aerosol particle emissions from
renewable diesel compared to ultra low sulfur diesel in at-sea operations of
a research vessel, Aerosol Sci. Tech., 51, 135–146,
https://doi.org/10.1080/02786826.2016.1238033, 2017.
Read, K. A., Lewis, A. C., Bauguitte, S., Rankin, A. M., Salmon, R. A.,
Wolff, E. W., Saiz-Lopez, A., Bloss, W. J., Heard, D. E., Lee, J. D., and
Plane, J. M. C.: DMS and MSA measurements in the Antarctic Boundary Layer:
impact of BrO on MSA production, Atmos. Chem. Phys., 8, 2985–2997,
https://doi.org/10.5194/acp-8-2985-2008, 2008.
Rickard, A. R., Wyche, K. P., Metzger, A., Monks, P. S., Ellis, A. M.,
Dommen, J., Baltensperger, U., Jenkin, M. E., and Pilling, M. J.: Gas phase
precursors to anthropogenic secondary organic aerosol Using the Master
Chemical Mechanism to probe detailed observations of 1,3,5-trimethylbenzene
photo-oxidation, Atmos. Environ., 44, 5423–5433,
https://doi.org/10.1016/j.atmosenv.2009.09.043, 2010.
Rickards, A. M. J., Miles, R. E. H., Davies, J. F., Marshall, F. H., and
Reid, J. P.: Measurements of the Sensitivity of Aerosol Hygroscopicity and
the kappa Parameter to the O ∕ C Ratio, J. Phys. Chem. A, 117,
14120–14131, https://doi.org/10.1021/jp407991n, 2013.
Riddick, S. N., Dragosits, U., Blackall, T. D., Daunt, F., Wanless, S., and
Sutton, M. A.: The global distribution of ammonia emissions from seabird
colonies, Atmos. Environ., 55, 319–327, https://doi.org/10.1016/j.atmosenv.2012.02.052,
2012.
Russell, L. M.: Aerosol organic-mass-to-organic-carbon ratio measurements,
Environ. Sci. Technol., 37, 2982–2987, 10.1021/es026123w, 2003.
Russell, L. M. and Shaw, G. E.: Arctic and Antarctic/Arctic Haze, in:
Encyclopedia of Atmospheric Sciences, 2nd Edn., edited by: North, G., Pyle,
J., and Zhang, F., Elsevier, UK and USA, 116–121, 2015.
Russell, L. M., Bahadur, R., Hawkins, L. N., Allan, J., Baumgardner, D.,
Quinn, P. K., and Bates, T. S.: Organic aerosol characterization by
complementary measurements of chemical bonds and molecular fragments, Atmos.
Environ., 43, 6100–6105, https://doi.org/10.1016/j.atmosenv.2009.09.036, 2009.
Russell, L. M., Hawkins, L. N., Frossard, A. A., Quinn, P. K., and Bates, T.
S.: Carbohydrate-like composition of submicron atmospheric particles and
their production from ocean bubble bursting, P. Natl. Acad. Sci. USA, 107,
6652–6657, https://doi.org/10.1073/pnas.0908905107, 2010.
Russell, L. M., Bahadur, R., and Ziemann, P. J.: Identifying organic aerosol
sources by comparing functional group composition in chamber and atmospheric
particles, P. Natl. Acad. Sci. USA, 108, 3516–3521,
https://doi.org/10.1073/pnas.1006461108, 2011.
Saliba, G., Saleh, R., Zhao, Y. L., Presto, A. A., Larnbe, A. T., Frodin, B.,
Sardar, S., Maldonado, H., Maddox, C., May, A. A., Drozd, G. T., Goldstein,
A. H., Russell, L. M., Hagen, F., and Robinson, A. L.: Comparison of Gasoline
Direct-Injection (GDI) and Port Fuel Injection (PFI) Vehicle Emissions:
Emission Certification Standards, Cold-Start, Secondary Organic Aerosol
Formation Potential, and Potential Climate Impacts, Environ. Sci. Technol.,
51, 6542–6552, https://doi.org/10.1021/acs.est.6b06509, 2017.
Savoie, D., Prospero, J., Larsen, R., Huang, F., Izaguirre, M., Huang, T.,
Snowdon, T., Custals, L., and Sanderson, C.: Nitrogen and sulfur species in
Antarctic aerosols at Mawson, Palmer station, and Marsh (King George Island),
J. Atmos. Chem., 17, 95–122, 1993.
Sax, M., Zenobi, R., Baltensperger, U., and Kalberer, M.: Time resolved
infrared spectroscopic analysis of aerosol formed by photo-oxidation of
1,3,5-trimethylbenzene and alpha-pinene, Aerosol Sci. Tech., 39, 822–830,
https://doi.org/10.1080/02786820500257859, 2005.
Saxena, V. and Ruggiero, F.: Aerosol measurements at Palmer Station,
Antarctica, Contributions to Antarctic Research, I, 1–5, 1990.
Scalabrin, E., Zangrando, R., Barbaro, E., Kehrwald, N. M., Gabrieli, J.,
Barbante, C., and Gambaro, A.: Amino acids in Arctic aerosols, Atmos. Chem.
Phys., 12, 10453–10463, https://doi.org/10.5194/acp-12-10453-2012, 2012.
Schmale, J., Schneider, J., Nemitz, E., Tang, Y. S., Dragosits, U., Blackall,
T. D., Trathan, P. N., Phillips, G. J., Sutton, M., and Braban, C. F.:
Sub-Antarctic marine aerosol: dominant contributions from biogenic sources,
Atmos. Chem. Phys., 13, 8669–8694, https://doi.org/10.5194/acp-13-8669-2013,
2013.
Schmidt, R. A.: Estimates of threshold windspeed from particle sizes in
blowing snow, Cold Reg. Sci. Technol., 4, 187–193,
https://doi.org/10.1016/0165-232x(81)90003-3, 1981.
Shaw, P. M., Russell, L. M., Jefferson, A., and Quinn, P. K.: Arctic organic
aerosol measurements show particles from mixed combustion in spring haze and
from frost flowers in winter, Geophys. Res. Lett., 37, L10803,
https://doi.org/10.1029/2010gl042831, 2010.
Shi, J. H., Gao, H. W., Qi, J. H., Zhang, J., and Yao, X. H.: Sources,
compositions, and distributions of water-soluble organic nitrogen in aerosols
over the China Sea, J. Geophys. Res.-Atmos., 115, D17303,
https://doi.org/10.1029/2009jd013238, 2010.
Solomon, S., Sanders, R. W., Jakoubek, R. O., Arpag, K. H., Stephens, S. L.,
Keys, J. G., and Garcia, R. R.: Visible and near-ultraviolet spectroscopy at
McMurdo-station, Antarctica. 10. Reductions of stratospheric NO2 Due
to Pinatubo aerosols, J. Geophys. Res.-Atmos., 99, 3509–3516,
https://doi.org/10.1029/93jd03088, 1994.
Steig, E. J., Schneider, D. P., Rutherford, S. D., Mann, M. E., Comiso, J.
C., and Shindell, D. T.: Warming of the Antarctic ice-sheet surface since the
1957 International Geophysical Year, Nature, 457, 459–462,
https://doi.org/10.1038/nature07669, 2009.
Stephanou, E. G. and Stratigakis, N.: Oxocarboxylic and α,
ω-dicarboxylic acids: photooxidation products of biogenic unsaturated
fatty acids present in urban aerosols, Environ. Sci. Technol., 27,
1403–1407, 1993.
Stohl, A.: Characteristics of atmospheric transport into the Arctic
troposphere, J. Geophys. Res.-Atmos., 111, D11306, https://doi.org/10.1029/2005jd006888,
2006.
Stohl, A. and Sodemann, H.: Characteristics of atmospheric transport into the
Antarctic troposphere, J. Geophys. Res.-Atmos., 115, D02305,
https://doi.org/10.1029/2009jd012536, 2010.
Su, H., Rose, D., Cheng, Y. F., Gunthe, S. S., Massling, A., Stock, M.,
Wiedensohler, A., Andreae, M. O., and Pöschl, U.: Hygroscopicity
distribution concept for measurement data analysis and modeling of aerosol
particle mixing state with regard to hygroscopic growth and CCN activation,
Atmos. Chem. Phys., 10, 7489–7503, https://doi.org/10.5194/acp-10-7489-2010,
2010.
Takahama, S., Johnson, A., and Russell, L. M.: Quantification of carboxylic
and carbonyl functional groups in organic aerosol infrared absorbance
spectra, Aerosol Sci. Tech., 47, 310–325, https://doi.org/10.1080/02786826.2012.752065,
2013.
Thomas, D. N. and Dieckmann, G. S.: Sea ice: an introduction to its physics,
chemistry, biology and geology, John Wiley & Sons, 2008.
Tukey, J. W.: Exploratory Data Analysis, 1st Edn., Behavioral Science,
Addison-Wesley, Reading, MA, 1977.
Udisti, R., Dayan, U., Becagli, S., Busetto, M., Frosini, D., Legrand, M.,
Lucarelli, F., Preunkert, S., Severi, M., Traversi, R., and Vitale, V.: Sea
spray aerosol in central Antarctica. Present atmospheric behaviour and
implications for paleoclimatic reconstructions, Atmos. Environ., 52,
109–120, https://doi.org/10.1016/j.atmosenv.2011.10.018, 2012.
Usher, C. R., Michel, A. E., and Grassian, V. H.: Reactions on mineral dust,
Chem. Rev., 103, 4883–4939, https://doi.org/10.1021/cr020657y, 2003.
Velleman, P. F.: Robust nonlinear data smoothers – definitions and
recommendations, P. Natl. Acad. Sci. USA, 74, 434–436,
https://doi.org/10.1073/pnas.74.2.434, 1977.
Violaki, K., Zarbas, P., and Mihalopoulos, N.: Long-term measurements of
dissolved organic nitrogen (DON) in atmospheric deposition in the Eastern
Mediterranean: Fluxes, origin and biogeochemical implications, Mar. Chem.,
120, 179–186, https://doi.org/10.1016/j.marchem.2009.08.004, 2010.
Vu, D., Short, D., Karavalakis, G., Durbin, T. D., and Asa-Awuku, A.: Will
Aerosol Hygroscopicity Change with Biodiesel, Renewable Diesel Fuels and
Emission Control Technologies?, Environ. Sci. Technol., 51, 1580–1586,
https://doi.org/10.1021/acs.est.6b03908, 2017.
Wagenbach, D., Ducroz, F., Mulvaney, R., Keck, L., Minikin, A., Legrand, M.,
Hall, J. S., and Wolff, E. W.: Sea-salt aerosol in coastal Antarctic regions,
J. Geophys. Res.-Atmos., 103, 10961–10974, https://doi.org/10.1029/97jd01804, 1998.
Warburton, J. A.: Surface measurements of Aitken nuclei at McMurdo, Siple,
Byrd, and South-pole stations, Antarct. J. US, 8, 236–236, 1973.
Weber, R. J., McMurry, P. H., Mauldin, L., Tanner, D. J., Eisele, F. L.,
Brechtel, F. J., Kreidenweis, S. M., Kok, G. L., Schillawski, R. D., and
Baumgardner, D.: A study of new particle formation and growth involving
biogenic and trace gas species measured during ACE 1, J. Geophys.
Res.-Atmos., 103, 16385–16396, https://doi.org/10.1029/97jd02465, 1998.
Wedyan, M. A. and Preston, M. R.: The coupling of surface seawater organic
nitrogen and the marine aerosol as inferred from enantiomer-specific amino
acid analysis, Atmos. Environ., 42, 8698–8705,
https://doi.org/10.1016/j.atmosenv.2008.04.038, 2008.
Weller, R. and Wagenbach, D.: Year-round chemical aerosol records in
continental Antarctica obtained by automatic samplings, Tellus B, 59,
755–765, https://doi.org/10.1111/j.1600-0889.2007.00293.x, 2007.
Weller, R., Minikin, A., Petzold, A., Wagenbach, D., and König-Langlo,
G.: Characterization of long-term and seasonal variations of black carbon
(BC) concentrations at Neumayer, Antarctica, Atmos. Chem. Phys., 13,
1579–1590, https://doi.org/10.5194/acp-13-1579-2013, 2013.
Wex, H., McFiggans, G., Henning, S., and Stratmann, F.: Influence of the
external mixing state of atmospheric aerosol on derived CCN number
concentrations, Geophys. Res. Lett., 37, L10805, https://doi.org/10.1029/2010gl043337,
2010.
Wyche, K. P., Monks, P. S., Ellis, A. M., Cordell, R. L., Parker, A. E.,
Whyte, C., Metzger, A., Dommen, J., Duplissy, J., Prevot, A. S. H.,
Baltensperger, U., Rickard, A. R., and Wulfert, F.: Gas phase precursors to
anthropogenic secondary organic aerosol: detailed observations of
1,3,5-trimethylbenzene photooxidation, Atmos. Chem. Phys., 9, 635–665,
https://doi.org/10.5194/acp-9-635-2009, 2009.
Xu, G. J., Gao, Y., Lin, Q., Li, W., and Chen, L. Q.: Characteristics of
water-soluble inorganic and organic ions in aerosols over the Southern Ocean
and coastal East Antarctica during austral summer, J. Geophys. Res.-Atmos.,
118, 13303–13318, https://doi.org/10.1002/2013jd019496, 2013.
Yang, X., Pyle, J. A., and Cox, R. A.: Sea salt aerosol production and
bromine release: Role of snow on sea ice, Geophys. Res. Lett., 35, L16815,
https://doi.org/10.1029/2008gl034536, 2008.
Zangrando, R., Barbaro, E., Vecchiato, M., Kehrwald, N. M., Barbante, C., and
Gambaro, A.: Levoglucosan and phenols in Antarctic marine, coastal and
plateau aerosols, Sci. Total Environ., 544, 606–616,
https://doi.org/10.1016/j.scitotenv.2015.11.166, 2016.
Short summary
Observations of the organic components of the natural aerosol are scarce in Antarctica, which limits our understanding of natural aerosols and their connection to cloud albedo. We took yearlong measurements of organic aerosols at McMurdo Station. The natural organic aerosol was 150 times higher in summer than in winter. We showed the natural sources of OM were characterized by amide, which may be from seabird populations. Acid was high in summer and likely formed by secondary reactions.
Observations of the organic components of the natural aerosol are scarce in Antarctica, which...
Altmetrics
Final-revised paper
Preprint