Articles | Volume 16, issue 5
https://doi.org/10.5194/acp-16-3413-2016
© Author(s) 2016. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
https://doi.org/10.5194/acp-16-3413-2016
© Author(s) 2016. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Research article
| 
16 Mar 2016
Research article |
| 16 Mar 2016
A global simulation of brown carbon: implications for photochemistry and direct radiative effect
Duseong S. Jo
School of Earth and Environmental Science, Seoul National
University, Seoul, 151-747, Republic of Korea
School of Earth and Environmental Science, Seoul National
University, Seoul, 151-747, Republic of Korea
Seungun Lee
School of Earth and Environmental Science, Seoul National
University, Seoul, 151-747, Republic of Korea
Sang-Woo Kim
School of Earth and Environmental Science, Seoul National
University, Seoul, 151-747, Republic of Korea
Xiaolu Zhang
Department of Civil and Environmental Engineering,
University of California, Davis, CA, USA
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Atmos. Meas. Tech., 13, 4353–4392, https://doi.org/10.5194/amt-13-4353-2020, https://doi.org/10.5194/amt-13-4353-2020, 2020
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Teruyuki Nakajima, Monica Campanelli, Huizheng Che, Victor Estellés, Hitoshi Irie, Sang-Woo Kim, Jhoon Kim, Dong Liu, Tomoaki Nishizawa, Govindan Pandithurai, Vijay Kumar Soni, Boossarasiri Thana, Nas-Urt Tugjsurn, Kazuma Aoki, Sujung Go, Makiko Hashimoto, Akiko Higurashi, Stelios Kazadzis, Pradeep Khatri, Natalia Kouremeti, Rei Kudo, Franco Marenco, Masahiro Momoi, Shantikumar S. Ningombam, Claire L. Ryder, Akihiro Uchiyama, and Akihiro Yamazaki
Atmos. Meas. Tech., 13, 4195–4218, https://doi.org/10.5194/amt-13-4195-2020, https://doi.org/10.5194/amt-13-4195-2020, 2020
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This paper overviews the progress in sky radiometer technology and the development of the network called SKYNET. It is found that the technology has produced useful on-site calibration methods, retrieval algorithms, and data analyses from sky radiometer observations of aerosol, cloud, water vapor, and ozone. The paper also discusses current issues of SKYNET to provide better information for the community.
Martine Collaud Coen, Elisabeth Andrews, Andrés Alastuey, Todor Petkov Arsov, John Backman, Benjamin T. Brem, Nicolas Bukowiecki, Cédric Couret, Konstantinos Eleftheriadis, Harald Flentje, Markus Fiebig, Martin Gysel-Beer, Jenny L. Hand, András Hoffer, Rakesh Hooda, Christoph Hueglin, Warren Joubert, Melita Keywood, Jeong Eun Kim, Sang-Woo Kim, Casper Labuschagne, Neng-Huei Lin, Yong Lin, Cathrine Lund Myhre, Krista Luoma, Hassan Lyamani, Angela Marinoni, Olga L. Mayol-Bracero, Nikos Mihalopoulos, Marco Pandolfi, Natalia Prats, Anthony J. Prenni, Jean-Philippe Putaud, Ludwig Ries, Fabienne Reisen, Karine Sellegri, Sangeeta Sharma, Patrick Sheridan, James Patrick Sherman, Junying Sun, Gloria Titos, Elvis Torres, Thomas Tuch, Rolf Weller, Alfred Wiedensohler, Paul Zieger, and Paolo Laj
Atmos. Chem. Phys., 20, 8867–8908, https://doi.org/10.5194/acp-20-8867-2020, https://doi.org/10.5194/acp-20-8867-2020, 2020
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Kyunghwa Lee, Jinhyeok Yu, Sojin Lee, Mieun Park, Hun Hong, Soon Young Park, Myungje Choi, Jhoon Kim, Younha Kim, Jung-Hun Woo, Sang-Woo Kim, and Chul H. Song
Geosci. Model Dev., 13, 1055–1073, https://doi.org/10.5194/gmd-13-1055-2020, https://doi.org/10.5194/gmd-13-1055-2020, 2020
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For the purpose of providing reliable and robust air quality predictions, an operational air quality prediction system was developed for the main air quality criteria species in South Korea (PM10, PM2.5, CO, O3 and SO2) by preparing the initial conditions for model simulations via data assimilation using satellite- and ground-based observations. The performance of the developed air quality prediction system was evaluated using ground in situ data during the KORUS-AQ campaign period.
Yongjoo Choi, Yugo Kanaya, Seung-Myung Park, Atsushi Matsuki, Yasuhiro Sadanaga, Sang-Woo Kim, Itsushi Uno, Xiaole Pan, Meehye Lee, Hyunjae Kim, and Dong Hee Jung
Atmos. Chem. Phys., 20, 83–98, https://doi.org/10.5194/acp-20-83-2020, https://doi.org/10.5194/acp-20-83-2020, 2020
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The relationship between black carbon (BC) and carbon monoxide (CO) can differ by the different structure of fuel consumption. By investigating the representativeness of the BC and CO emission inventory for real-world comparison with reliable observations, this study suggested that accurate CO emissions should be preferentially investigated to enhance the accuracy of the BC emission rate over East Asia.
Hyeong-Ahn Kwon, Rokjin J. Park, Gonzalo González Abad, Kelly Chance, Thomas P. Kurosu, Jhoon Kim, Isabelle De Smedt, Michel Van Roozendael, Enno Peters, and John Burrows
Atmos. Meas. Tech., 12, 3551–3571, https://doi.org/10.5194/amt-12-3551-2019, https://doi.org/10.5194/amt-12-3551-2019, 2019
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The Geostationary Environment Monitoring Spectrometer (GEMS) will be launched by South Korea in 2019, and it will measure radiances ranging from 300 to 500 nm every hour with a fine spatial resolution of 7 km x 8 km over Seoul in South Korea to monitor column concentrations of air pollutants including O3, NO2, SO2, and HCHO, as well as aerosol optical properties. This paper describes a GEMS formaldehyde retrieval algorithm including a number of sensitivity tests for algorithm evaluation.
Seohui Park, Minso Shin, Jungho Im, Chang-Keun Song, Myungje Choi, Jhoon Kim, Seungun Lee, Rokjin Park, Jiyoung Kim, Dong-Won Lee, and Sang-Kyun Kim
Atmos. Chem. Phys., 19, 1097–1113, https://doi.org/10.5194/acp-19-1097-2019, https://doi.org/10.5194/acp-19-1097-2019, 2019
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This study proposed machine-learning-based models to estimate ground-level particulate matter concentrations using satellite observations and numerical model-derived data. Aerosol optical depth was identified as the most significant for estimating ground-level PM concentrations, followed by wind speed and solar radiation. The results show that the proposed models produced better performance than the existing approaches, particularly in improving on the biases of the process-based models.
Arlene M. Fiore, Emily V. Fischer, George P. Milly, Shubha Pandey Deolal, Oliver Wild, Daniel A. Jaffe, Johannes Staehelin, Olivia E. Clifton, Dan Bergmann, William Collins, Frank Dentener, Ruth M. Doherty, Bryan N. Duncan, Bernd Fischer, Stefan Gilge, Peter G. Hess, Larry W. Horowitz, Alexandru Lupu, Ian A. MacKenzie, Rokjin Park, Ludwig Ries, Michael G. Sanderson, Martin G. Schultz, Drew T. Shindell, Martin Steinbacher, David S. Stevenson, Sophie Szopa, Christoph Zellweger, and Guang Zeng
Atmos. Chem. Phys., 18, 15345–15361, https://doi.org/10.5194/acp-18-15345-2018, https://doi.org/10.5194/acp-18-15345-2018, 2018
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We demonstrate a proof-of-concept approach for applying northern midlatitude mountaintop peroxy acetyl nitrate (PAN) measurements and a multi-model ensemble during April to constrain the influence of continental-scale anthropogenic precursor emissions on PAN. Our findings imply a role for carefully coordinated multi-model ensembles in helping identify observations for discriminating among widely varying (and poorly constrained) model responses of atmospheric constituents to changes in emissions.
Ciao-Kai Liang, J. Jason West, Raquel A. Silva, Huisheng Bian, Mian Chin, Yanko Davila, Frank J. Dentener, Louisa Emmons, Johannes Flemming, Gerd Folberth, Daven Henze, Ulas Im, Jan Eiof Jonson, Terry J. Keating, Tom Kucsera, Allen Lenzen, Meiyun Lin, Marianne Tronstad Lund, Xiaohua Pan, Rokjin J. Park, R. Bradley Pierce, Takashi Sekiya, Kengo Sudo, and Toshihiko Takemura
Atmos. Chem. Phys., 18, 10497–10520, https://doi.org/10.5194/acp-18-10497-2018, https://doi.org/10.5194/acp-18-10497-2018, 2018
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Emissions from one continent affect air quality and health elsewhere. Here we quantify the effects of intercontinental PM2.5 and ozone transport on human health using a new multi-model ensemble, evaluating the health effects of emissions from six world regions and three emission source sectors. Emissions from one region have significant health impacts outside of that source region; similarly, foreign emissions contribute significantly to air-pollution-related deaths in several world regions.
Si-Wan Kim, Vijay Natraj, Seoyoung Lee, Hyeong-Ahn Kwon, Rokjin Park, Joost de Gouw, Gregory Frost, Jhoon Kim, Jochen Stutz, Michael Trainer, Catalina Tsai, and Carsten Warneke
Atmos. Chem. Phys., 18, 7639–7655, https://doi.org/10.5194/acp-18-7639-2018, https://doi.org/10.5194/acp-18-7639-2018, 2018
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Formaldehyde (HCHO) is a hazardous air pollutant and is associated with tropospheric ozone production. HCHO has been monitored from space. In this study, to acquire high-quality satellite-based HCHO observations, we utilize fine-resolution atmospheric chemistry model results as an input to the computer code for satellite retrievals over the Los Angeles Basin. Our study indicates that the use of fine-resolution profile shapes helps to identify HCHO plumes from space.
Christian Hogrefe, Peng Liu, George Pouliot, Rohit Mathur, Shawn Roselle, Johannes Flemming, Meiyun Lin, and Rokjin J. Park
Atmos. Chem. Phys., 18, 3839–3864, https://doi.org/10.5194/acp-18-3839-2018, https://doi.org/10.5194/acp-18-3839-2018, 2018
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This study quantifies the impacts of different representations of background ozone in state-of-the-science large-scale models on surface and aloft ozone burdens simulated by the CMAQ regional model over the United States. It also compares both the CMAQ simulations and the driving large-scale models to surface and upper air observations.
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
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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.
Gouri Prabhakar, Caroline L. Parworth, Xiaolu Zhang, Hwajin Kim, Dominique E. Young, Andreas J. Beyersdorf, Luke D. Ziemba, John B. Nowak, Timothy H. Bertram, Ian C. Faloona, Qi Zhang, and Christopher D. Cappa
Atmos. Chem. Phys., 17, 14747–14770, https://doi.org/10.5194/acp-17-14747-2017, https://doi.org/10.5194/acp-17-14747-2017, 2017
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This work assesses the processes that control the ambient concentrations of particulate nitrate in the the wintertime San Joaquin Valley of California through a combination of aircraft and surface measurements made during the DISCOVER-AQ study. We provide an observational demonstration of how nocturnal production and advection in aloft layers combines with daytime production and loss from entrainment and deposition to give rise to a distinct diurnal profile in surface nitrate concentrations.
Duseong S. Jo, Rokjin J. Park, Jaein I. Jeong, Gabriele Curci, Hyung-Min Lee, and Sang-Woo Kim
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2017-1104, https://doi.org/10.5194/acp-2017-1104, 2017
Preprint retracted
Chaeyoon Cho, Sang-Woo Kim, Maheswar Rupakheti, Jin-Soo Park, Arnico Panday, Soon-Chang Yoon, Ji-Hyoung Kim, Hyunjae Kim, Haeun Jeon, Minyoung Sung, Bong Mann Kim, Seungkyu K. Hong, Rokjin J. Park, Dipesh Rupakheti, Khadak Singh Mahata, Puppala Siva Praveen, Mark G. Lawrence, and Brent Holben
Atmos. Chem. Phys., 17, 12617–12632, https://doi.org/10.5194/acp-17-12617-2017, https://doi.org/10.5194/acp-17-12617-2017, 2017
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We investigated the optical and chemical properties and direct radiative effects of aerosols in the Kathmandu Valley. We concluded that the ratio of light-absorbing to scattering aerosols as well as the concentration of light-absorbing aerosols is much higher at Kathmandu than other comparable regions, and it contributes to a great atmospheric absorption efficiency. This study provides unprecedented insights into aerosol optical properties and their radiative forcings in the Kathmandu Valley.
Lauren Schmeisser, Elisabeth Andrews, John A. Ogren, Patrick Sheridan, Anne Jefferson, Sangeeta Sharma, Jeong Eun Kim, James P. Sherman, Mar Sorribas, Ivo Kalapov, Todor Arsov, Christo Angelov, Olga L. Mayol-Bracero, Casper Labuschagne, Sang-Woo Kim, András Hoffer, Neng-Huei Lin, Hao-Ping Chia, Michael Bergin, Junying Sun, Peng Liu, and Hao Wu
Atmos. Chem. Phys., 17, 12097–12120, https://doi.org/10.5194/acp-17-12097-2017, https://doi.org/10.5194/acp-17-12097-2017, 2017
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Three methods are used to classify aerosol type from aerosol optical properties measured in situ at 24 surface sites. Classification methods work best at sites with stable, homogenous aerosol at particularly polluted and dust-prone continental and marine sites. Classification methods are poor at remote marine and Arctic sites. Using these methods to extrapolate aerosol type from optical properties can help determine aerosol radiative forcing and improve aerosol satellite retrieval algorithms.
Min Huang, Gregory R. Carmichael, R. Bradley Pierce, Duseong S. Jo, Rokjin J. Park, Johannes Flemming, Louisa K. Emmons, Kevin W. Bowman, Daven K. Henze, Yanko Davila, Kengo Sudo, Jan Eiof Jonson, Marianne Tronstad Lund, Greet Janssens-Maenhout, Frank J. Dentener, Terry J. Keating, Hilke Oetjen, and Vivienne H. Payne
Atmos. Chem. Phys., 17, 5721–5750, https://doi.org/10.5194/acp-17-5721-2017, https://doi.org/10.5194/acp-17-5721-2017, 2017
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In support of the HTAP phase 2 experiment, we conducted a number of regional-scale Sulfur Transport and dEposition Model base and sensitivity simulations over North America during May–June 2010. The STEM chemical boundary conditions were downscaled from three (GEOS-Chem, RAQMS, and ECMWF C-IFS) global chemical transport models' simulations. Analyses were performed on large spatial–temporal scales relative to HTAP1 and also on subcontinental and event scales including the use of satellite data.
Hyeong-Ahn Kwon, Rokjin J. Park, Jaein I. Jeong, Seungun Lee, Gonzalo González Abad, Thomas P. Kurosu, Paul I. Palmer, and Kelly Chance
Atmos. Chem. Phys., 17, 4673–4686, https://doi.org/10.5194/acp-17-4673-2017, https://doi.org/10.5194/acp-17-4673-2017, 2017
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A geostationary satellite can measure daytime hourly HCHO columns. Atmospheric conditions such as synoptic meteorology and the presence of other gases and aerosols may affect HCHO measurements. We examine the effects of their temporal variation on the HCHO measurement of a geostationary satellite in East Asia. We find that the hourly variation of other species could be important. Especially the inclusion of hourly aerosol variation in the retrieval could lead to improving HCHO measurements.
B. Quennehen, J.-C. Raut, K. S. Law, N. Daskalakis, G. Ancellet, C. Clerbaux, S.-W. Kim, M. T. Lund, G. Myhre, D. J. L. Olivié, S. Safieddine, R. B. Skeie, J. L. Thomas, S. Tsyro, A. Bazureau, N. Bellouin, M. Hu, M. Kanakidou, Z. Klimont, K. Kupiainen, S. Myriokefalitakis, J. Quaas, S. T. Rumbold, M. Schulz, R. Cherian, A. Shimizu, J. Wang, S.-C. Yoon, and T. Zhu
Atmos. Chem. Phys., 16, 10765–10792, https://doi.org/10.5194/acp-16-10765-2016, https://doi.org/10.5194/acp-16-10765-2016, 2016
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This paper evaluates the ability of six global models and one regional model in reproducing short-lived pollutants (defined here as ozone and its precursors, aerosols and black carbon) concentrations over Asia using satellite, ground-based and airborne observations.
Key findings are that models homogeneously reproduce the trace gas observations although nitrous oxides are underestimated, whereas the aerosol distributions are heterogeneously reproduced, implicating important uncertainties.
Alma Hodzic, Prasad S. Kasibhatla, Duseong S. Jo, Christopher D. Cappa, Jose L. Jimenez, Sasha Madronich, and Rokjin J. Park
Atmos. Chem. Phys., 16, 7917–7941, https://doi.org/10.5194/acp-16-7917-2016, https://doi.org/10.5194/acp-16-7917-2016, 2016
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The global budget and spatial distribution of secondary organic aerosol (SOA) are highly uncertain in chemistry-climate models, which reflects our inability to characterize all phases of the OA lifecycle. We have performed global model simulations with the newly proposed formation and removal processes (photolysis and heterogeneous chemistry) and shown that SOA is a far more dynamic system, with 4 times stronger production rates and more efficient removal mechanisms, than assumed in models.
Christopher D. Cappa, Katheryn R. Kolesar, Xiaolu Zhang, Dean B. Atkinson, Mikhail S. Pekour, Rahul A. Zaveri, Alla Zelenyuk, and Qi Zhang
Atmos. Chem. Phys., 16, 6511–6535, https://doi.org/10.5194/acp-16-6511-2016, https://doi.org/10.5194/acp-16-6511-2016, 2016
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Measurements of size-dependent aerosol optical properties at visible wavelengths made during the 2010 CARES study are reported on, with a special focus on the characterization of supermicron particles. The relationships with and dependence upon particle composition, particle size, photochemical aging, water uptake and heating are discussed, along with broader implications of these in situ measurements for the interpretation of remote sensing products.
Dominique E. Young, Hwajin Kim, Caroline Parworth, Shan Zhou, Xiaolu Zhang, Christopher D. Cappa, Roger Seco, Saewung Kim, and Qi Zhang
Atmos. Chem. Phys., 16, 5427–5451, https://doi.org/10.5194/acp-16-5427-2016, https://doi.org/10.5194/acp-16-5427-2016, 2016
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Aerosol chemistry and the sources and processes driving the observed temporal and diurnal variations of PM were studied in a polluted urban environment during winter 2013. These results were compared to a similar campaign from winter 2010. Meteorology strongly influenced PM composition, both directly and indirectly. Nighttime reactions played a more important role in 2013 and the influence from a nighttime formed residual layer that mixed down in the morning was also much more intense in 2013.
Z. L. Lüthi, B. Škerlak, S.-W. Kim, A. Lauer, A. Mues, M. Rupakheti, and S. Kang
Atmos. Chem. Phys., 15, 6007–6021, https://doi.org/10.5194/acp-15-6007-2015, https://doi.org/10.5194/acp-15-6007-2015, 2015
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The Himalayas and the Tibetan Plateau region (HTP) is regularly exposed to polluted air masses that might influence glaciers as well as climate on regional to global scales. We found that atmospheric brown clouds from South Asia reach the HTP by crossing the Himalayas not only through the major north--south river valleys but rather over large areas by being lifted and advected at mid-troposheric levels. The transport is enabled by a combination of synoptic and local meteorological settings.
S. Seo, J. Kim, H. Lee, U. Jeong, W. Kim, B. N. Holben, S.-W. Kim, C. H. Song, and J. H. Lim
Atmos. Chem. Phys., 15, 319–334, https://doi.org/10.5194/acp-15-319-2015, https://doi.org/10.5194/acp-15-319-2015, 2015
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The estimation of PM10 from optical measurement of AERONET and MODIS by various empirical models was evaluated for the DRAGON-Asia campaign. The results showed the importance of boundary layer height (BLH) and effective radius (Reff) in estimating PM10. The highest correlation between the estimated and measured values was found to be 0.81 in winter due to the stagnant air mass and low BLH, while the poorest values were 0.54 in spring due to the influence of long-range transport above BLH.
R. J. Park, S. K. Hong, H.-A. Kwon, S. Kim, A. Guenther, J.-H. Woo, and C. P. Loughner
Atmos. Chem. Phys., 14, 7929–7940, https://doi.org/10.5194/acp-14-7929-2014, https://doi.org/10.5194/acp-14-7929-2014, 2014
S. Lim, M. Lee, S.-W. Kim, S.-C. Yoon, G. Lee, and Y. J. Lee
Atmos. Chem. Phys., 14, 7781–7793, https://doi.org/10.5194/acp-14-7781-2014, https://doi.org/10.5194/acp-14-7781-2014, 2014
J. Jung, H. Furutani, M. Uematsu, S. Kim, and S. Yoon
Atmos. Chem. Phys., 13, 411–428, https://doi.org/10.5194/acp-13-411-2013, https://doi.org/10.5194/acp-13-411-2013, 2013
Related subject area
Subject: Aerosols | Research Activity: Atmospheric Modelling and Data Analysis | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Analysis of secondary inorganic aerosols over the greater Athens area using the EPISODE–CityChem source dispersion and photochemistry model
Global estimates of ambient reactive nitrogen components during 2000–2100 based on the multi-stage model
The role of naphthalene and its derivatives in the formation of secondary organic aerosol in the Yangtze River Delta region, China
Unveiling the optimal regression model for source apportionment of the oxidative potential of PM10
Investigating the contribution of grown new particles to cloud condensation nuclei with largely varying preexisting particles – Part 2: Modeling chemical drivers and 3-D new particle formation occurrence
Technical note: Influence of different averaging metrics and temporal resolutions on the aerosol pH calculated by thermodynamic modeling
Dual roles of the inorganic aqueous phase on secondary organic aerosol growth from benzene and phenol
Global source apportionment of aerosols into major emission regions and sectors over 1850–2017
Modeling atmospheric brown carbon in the GISS ModelE Earth system model
Observation-constrained kinetic modeling of isoprene SOA formation in the atmosphere
Significant impact of urban tree biogenic emissions on air quality estimated by a bottom-up inventory and chemistry transport modeling
Secondary organic aerosols derived from intermediate-volatility n-alkanes adopt low-viscous phase state
Cooling radiative forcing effect enhancement of atmospheric amines-mineral particle caused by heterogeneous uptake and oxidation
Modeling the drivers of fine PM pollution over Central Europe: impacts and contributions of emissions from different sources
Reaction of SO3 with H2SO4 and its implications for aerosol particle formation in the gas phase and at the air–water interface
Weakened aerosol–radiation interaction exacerbating ozone pollution in eastern China since China's clean air actions
Uncertainties from biomass burning aerosols in air quality models obscure public health impacts in Southeast Asia
Oxidative potential apportionment of atmospheric PM1: a new approach combining high-sensitive online analysers for chemical composition and offline OP measurement technique
Observed and CMIP6 model simulated organic aerosol response to drought in the contiguous United States during summertime
Aqueous-phase chemistry of glyoxal with multifunctional reduced nitrogen compounds: a potential missing route for secondary brown carbon
An updated modeling framework to simulate Los Angeles air quality – Part 1: Model development, evaluation, and source apportionment
Frequent haze events associated with transport and stagnation over the corridor between the North China Plain and Yangtze River Delta
Evaluation of WRF-Chem-simulated meteorology and aerosols over northern India during the severe pollution episode of 2016
How well are aerosol–cloud interactions represented in climate models? – Part 1: Understanding the sulfate aerosol production from the 2014–15 Holuhraun eruption
pH regulates the formation of organosulfates and inorganic sulfate from organic peroxide reaction with dissolved SO2 in aquatic media
Technical note: Accurate, reliable, and high-resolution air quality predictions by improving the Copernicus Atmosphere Monitoring Service using a novel statistical post-processing method
Contribution of intermediate-volatility organic compounds from on-road transport to secondary organic aerosol levels in Europe
Source-resolved atmospheric metal emissions, concentrations, and their deposition fluxes into the East Asian Seas
Development of an integrated model framework for multi-air-pollutant exposure assessments in high-density cities
CAMx–UNIPAR simulation of secondary organic aerosol mass formed from multiphase reactions of hydrocarbons under the Central Valley urban atmospheres of California
Impact of urbanization on fine particulate matter concentrations over central Europe
Measurement report: Assessing the impacts of emission uncertainty on aerosol optical properties and radiative forcing from biomass burning in peninsular Southeast Asia
The Emissions Model Intercomparison Project (Emissions-MIP): quantifying model sensitivity to emission characteristics
Dynamics-based estimates of decline trend with fine temporal variations in China's PM2.5 emissions
Effects of simulated secondary organic aerosol water on PM1 levels and composition over the US
Reactive organic carbon air emissions from mobile sources in the United States
Development and evaluation of processes affecting simulation of diel fine particulate matter variation in the GEOS-Chem model
Substantially positive contributions of new particle formation to cloud condensation nuclei under low supersaturation in China based on numerical model improvements
Evolution of atmospheric age of particles and its implications for the formation of a severe haze event in eastern China
A multimodel evaluation of the potential impact of shipping on particle species in the Mediterranean Sea
How does tropospheric VOC chemistry affect climate? An investigation of preindustrial control simulations using the Community Earth System Model version 2
Anthropogenic amplification of biogenic secondary organic aerosol production
A dynamic parameterization of sulfuric acid–dimethylamine nucleation and its application in three-dimensional modeling
Modeling dust mineralogical composition: sensitivity to soil mineralogy atlases and their expected climate impacts
Assessment of the impacts of cloud chemistry on surface SO2 and sulfate levels in typical regions of China
Impact of Landes forest fires on air quality in France during the 2022 summer
Global nitrogen and sulfur deposition mapping using a measurement–model fusion approach
Comprehensive simulations of new particle formation events in Beijing with a cluster dynamics–multicomponent sectional model
Implications of differences between recent anthropogenic aerosol emission inventories for diagnosed AOD and radiative forcing from 1990 to 2019
Unbalanced emission reductions of different species and sectors in China during COVID-19 lockdown derived by multi-species surface observation assimilation
Stelios Myriokefalitakis, Matthias Karl, Kim A. Weiss, Dimitris Karagiannis, Eleni Athanasopoulou, Anastasia Kakouri, Aikaterini Bougiatioti, Eleni Liakakou, Iasonas Stavroulas, Georgios Papangelis, Georgios Grivas, Despina Paraskevopoulou, Orestis Speyer, Nikolaos Mihalopoulos, and Evangelos Gerasopoulos
Atmos. Chem. Phys., 24, 7815–7835, https://doi.org/10.5194/acp-24-7815-2024, https://doi.org/10.5194/acp-24-7815-2024, 2024
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A state-of-the-art thermodynamic model has been coupled with the city-scale chemistry transport model EPISODE–CityChem to investigate the equilibrium between the inorganic gas and aerosol phases over the greater Athens area, Greece. The simulations indicate that the formation of nitrates in an urban environment is significantly affected by local nitrogen oxide emissions, as well as ambient temperature, relative humidity, photochemical activity, and the presence of non-volatile cations.
Rui Li, Yining Gao, Lijia Zhang, Yubing Shen, Tianzhao Xu, Wenwen Sun, and Gehui Wang
Atmos. Chem. Phys., 24, 7623–7636, https://doi.org/10.5194/acp-24-7623-2024, https://doi.org/10.5194/acp-24-7623-2024, 2024
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A three-stage model was developed to obtain the global maps of reactive nitrogen components during 2000–2100. The results implied that cross-validation R2 values of four species showed satisfactory performance (R2 > 0.55). Most reactive nitrogen components, except NH3, in China showed increases during 2000–2013. In the future scenarios, SSP3-7.0 (traditional-energy scenario) and SSP1-2.6 (carbon neutrality scenario) showed the highest and lowest reactive nitrogen component concentrations.
Fei Ye, Jingyi Li, Yaqin Gao, Hongli Wang, Jingyu An, Cheng Huang, Song Guo, Keding Lu, Kangjia Gong, Haowen Zhang, Momei Qin, and Jianlin Hu
Atmos. Chem. Phys., 24, 7467–7479, https://doi.org/10.5194/acp-24-7467-2024, https://doi.org/10.5194/acp-24-7467-2024, 2024
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Naphthalene (Nap) and methylnaphthalene (MN) are key precursors of secondary organic aerosol (SOA), yet their sources and sinks are often inadequately represented in air quality models. In this study, we incorporated detailed emissions, gas-phase chemistry, and SOA parameterization of Nap and MN into CMAQ to address this issue. The findings revealed remarkably high SOA formation potentials for these compounds despite their low emissions in the Yangtze River Delta region during summer.
Vy Dinh Ngoc Thuy, Jean-Luc Jaffrezo, Ian Hough, Pamela A. Dominutti, Guillaume Salque Moreton, Grégory Gille, Florie Francony, Arabelle Patron-Anquez, Olivier Favez, and Gaëlle Uzu
Atmos. Chem. Phys., 24, 7261–7282, https://doi.org/10.5194/acp-24-7261-2024, https://doi.org/10.5194/acp-24-7261-2024, 2024
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The capacity of particulate matter (PM) to generate reactive oxygen species in vivo is represented by oxidative potential (OP). This study focuses on finding the appropriate model to evaluate the oxidative character of PM sources in six sites using the PM sources and OP. Eight regression techniques are introduced to assess the OP of PM. The study highlights the importance of selecting a model according to the input data characteristics and establishes some recommendations for the procedure.
Ming Chu, Xing Wei, Shangfei Hai, Yang Gao, Huiwang Gao, Yujiao Zhu, Biwu Chu, Nan Ma, Juan Hong, Yele Sun, and Xiaohong Yao
Atmos. Chem. Phys., 24, 6769–6786, https://doi.org/10.5194/acp-24-6769-2024, https://doi.org/10.5194/acp-24-6769-2024, 2024
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We used a 20-bin WRF-Chem model to simulate NPF events in the NCP during a three-week observational period in the summer of 2019. The model was able to reproduce the observations during June 29–July 6, which was characterized by a high frequency of NPF occurrence.
Haoqi Wang, Xiao Tian, Wanting Zhao, Jiacheng Li, Haoyu Yu, Yinchang Feng, and Shaojie Song
Atmos. Chem. Phys., 24, 6583–6592, https://doi.org/10.5194/acp-24-6583-2024, https://doi.org/10.5194/acp-24-6583-2024, 2024
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pH is a key property of ambient aerosols, which affect many atmospheric processes. As aerosol pH is a non-conservative parameter, diverse averaging metrics and temporal resolutions may influence the pH values calculated by thermodynamic models. This technical note seeks to quantitatively evaluate the average pH using varied metrics and resolutions. The ultimate goal is to establish standardized reporting practices in future research endeavors.
Jiwon Choi, Myoseon Jang, and Spencer Blau
Atmos. Chem. Phys., 24, 6567–6582, https://doi.org/10.5194/acp-24-6567-2024, https://doi.org/10.5194/acp-24-6567-2024, 2024
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Persistent phenoxy radical (PPR), formed by phenol gas oxidation and its aqueous reaction, catalytically destroys O3 and retards secondary organic aerosol (SOA) growth. Explicit gas mechanisms including the formation of PPR and low-volatility products from the oxidation of phenol or benzene are applied to the UNIPAR model to predict SOA mass via multiphase reactions of precursors. Aqueous reactions of reactive organics increase SOA mass but retard SOA growth via heterogeneously formed PPR.
Yang Yang, Shaoxuan Mou, Hailong Wang, Pinya Wang, Baojie Li, and Hong Liao
Atmos. Chem. Phys., 24, 6509–6523, https://doi.org/10.5194/acp-24-6509-2024, https://doi.org/10.5194/acp-24-6509-2024, 2024
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The variations in anthropogenic aerosol concentrations and source contributions and their subsequent radiative impact in major emission regions during historical periods are quantified based on an aerosol-tagging system in E3SMv1. Due to the industrial development and implementation of economic policies, sources of anthropogenic aerosols show different variations, which has important implications for pollution prevention and control measures and decision-making for global collaboration.
Maegan A. DeLessio, Kostas Tsigaridis, Susanne E. Bauer, Jacek Chowdhary, and Gregory L. Schuster
Atmos. Chem. Phys., 24, 6275–6304, https://doi.org/10.5194/acp-24-6275-2024, https://doi.org/10.5194/acp-24-6275-2024, 2024
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This study presents the first explicit representation of brown carbon aerosols in the GISS ModelE Earth system model (ESM). Model sensitivity to a range of brown carbon parameters and model performance compared to AERONET and MODIS retrievals of total aerosol properties were assessed. A summary of best practices for incorporating brown carbon into ModelE is also included.
Chuanyang Shen, Xiaoyan Yang, Joel Thornton, John Shilling, Chenyang Bi, Gabriel Isaacman-VanWertz, and Haofei Zhang
Atmos. Chem. Phys., 24, 6153–6175, https://doi.org/10.5194/acp-24-6153-2024, https://doi.org/10.5194/acp-24-6153-2024, 2024
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In this work, a condensed multiphase isoprene oxidation mechanism was developed to simulate isoprene SOA formation from chamber and field studies. Our results show that the measured isoprene SOA mass concentrations can be reasonably reproduced. The simulation results indicate that multifunctional low-volatility products contribute significantly to total isoprene SOA. Our findings emphasize that the pathways to produce these low-volatility species should be considered in models.
Alice Maison, Lya Lugon, Soo-Jin Park, Alexia Baudic, Christopher Cantrell, Florian Couvidat, Barbara D'Anna, Claudia Di Biagio, Aline Gratien, Valérie Gros, Carmen Kalalian, Julien Kammer, Vincent Michoud, Jean-Eudes Petit, Marwa Shahin, Leila Simon, Myrto Valari, Jérémy Vigneron, Andrée Tuzet, and Karine Sartelet
Atmos. Chem. Phys., 24, 6011–6046, https://doi.org/10.5194/acp-24-6011-2024, https://doi.org/10.5194/acp-24-6011-2024, 2024
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This study presents the development of a bottom-up inventory of urban tree biogenic emissions. Emissions are computed for each tree based on their location and characteristics and are integrated in the regional air quality model WRF-CHIMERE. The impact of these biogenic emissions on air quality is quantified for June–July 2022. Over Paris city, urban trees increase the concentrations of particulate organic matter by 4.6 %, of PM2.5 by 0.6 %, and of ozone by 1.0 % on average over 2 months.
Tommaso Galeazzo, Bernard Aumont, Marie Camredon, Richard Valorso, Yong B. Lim, Paul J. Ziemann, and Manabu Shiraiwa
Atmos. Chem. Phys., 24, 5549–5565, https://doi.org/10.5194/acp-24-5549-2024, https://doi.org/10.5194/acp-24-5549-2024, 2024
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Secondary organic aerosol (SOA) derived from n-alkanes is a major component of anthropogenic particulate matter. We provide an analysis of n-alkane SOA by chemistry modeling, machine learning, and laboratory experiments, showing that n-alkane SOA adopts low-viscous semi-solid or liquid states. Our results indicate few kinetic limitations of mass accommodation in SOA formation, supporting the application of equilibrium partitioning for simulating n-alkane SOA in large-scale atmospheric models.
Weina Zhang, Jianhua Mai, Zhichao Fan, Yongpeng Ji, Yuemeng Ji, Guiying Li, Yanpeng Gao, and Taicheng An
EGUsphere, https://doi.org/10.5194/egusphere-2024-1048, https://doi.org/10.5194/egusphere-2024-1048, 2024
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Previous studies show distinctive RFE of AOP-mineral mixed particles from individual mineral or AOP particles. This study reveals heterogeneous oxidation causes further RFE enhancement of amine-mineral mixed particle. Note that RFE increment is higher under clean condition than that under polluted condition, which is contributed to high-oxygen-content product. The enhanced RFE of amine-mineral particle caused by heterogenous oxidation is expected to alleviate warming effect.
Lukáš Bartík, Peter Huszár, Jan Karlický, Ondřej Vlček, and Kryštof Eben
Atmos. Chem. Phys., 24, 4347–4387, https://doi.org/10.5194/acp-24-4347-2024, https://doi.org/10.5194/acp-24-4347-2024, 2024
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The presented study deals with the attribution of fine particulate matter (PM2.5) concentrations to anthropogenic emissions over Central Europe using regional-scale models. It calculates the present-day contributions of different emissions sectors to concentrations of PM2.5 and its secondary components. Moreover, the study investigates the effect of chemical nonlinearities by using multiple source attribution methods and secondary organic aerosol calculation methods.
Rui Wang, Yang Cheng, Shasha Chen, Rongrong Li, Yue Hu, Xiaokai Guo, Tianlei Zhang, Fengmin Song, and Hao Li
Atmos. Chem. Phys., 24, 4029–4046, https://doi.org/10.5194/acp-24-4029-2024, https://doi.org/10.5194/acp-24-4029-2024, 2024
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We used quantum chemical calculations, Born–Oppenheimer molecular dynamics simulations, and the ACDC kinetic model to characterize SO3–H2SO4 interaction in the gas phase and at the air–water interface and to study the effect of H2S2O7 on H2SO4–NH3-based clusters. The work expands our understanding of new pathways for the loss of SO3 in acidic polluted areas and helps reveal some missing sources of NPF in metropolitan industrial regions and understand the atmospheric organic–sulfur cycle better.
Hao Yang, Lei Chen, Hong Liao, Jia Zhu, Wenjie Wang, and Xin Li
Atmos. Chem. Phys., 24, 4001–4015, https://doi.org/10.5194/acp-24-4001-2024, https://doi.org/10.5194/acp-24-4001-2024, 2024
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The present study quantifies the response of aerosol–radiation interaction (ARI) to anthropogenic emission reduction from 2013 to 2017, with the main focus on the contribution to changed O3 concentrations over eastern China both in summer and winter using the WRF-Chem model. The weakened ARI due to decreased anthropogenic emission aggravates the summer (winter) O3 pollution by +0.81 ppb (+0.63 ppb), averaged over eastern China.
Margaret R. Marvin, Paul I. Palmer, Fei Yao, Mohd Talib Latif, and Md Firoz Khan
Atmos. Chem. Phys., 24, 3699–3715, https://doi.org/10.5194/acp-24-3699-2024, https://doi.org/10.5194/acp-24-3699-2024, 2024
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We use an atmospheric chemistry model to investigate aerosols emitted from fire activity across Southeast Asia. We find that the limited nature of measurements in this region leads to large uncertainties that significantly hinder the model representation of these aerosols and their impacts on air quality. As a result, the number of monthly attributable deaths is underestimated by as many as 4500, particularly in March at the peak of the mainland burning season.
Julie Camman, Benjamin Chazeau, Nicolas Marchand, Amandine Durand, Grégory Gille, Ludovic Lanzi, Jean-Luc Jaffrezo, Henri Wortham, and Gaëlle Uzu
Atmos. Chem. Phys., 24, 3257–3278, https://doi.org/10.5194/acp-24-3257-2024, https://doi.org/10.5194/acp-24-3257-2024, 2024
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Fine particle (PM1) pollution is a major health issue in the city of Marseille, which is subject to numerous pollution sources. Sampling carried out during the summer enabled a fine characterization of the PM1 sources and their oxidative potential, a promising new metric as a proxy for health impact. PM1 came mainly from combustion sources, secondary ammonium sulfate, and organic nitrate, while the oxidative potential of PM1 came from these sources and from resuspended dust in the atmosphere.
Wei Li and Yuxuan Wang
EGUsphere, https://doi.org/10.5194/egusphere-2024-430, https://doi.org/10.5194/egusphere-2024-430, 2024
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This study finds that droughts immensely increased organic aerosol (OA) in the contiguous U.S. during summertime 1998–2019, notably in the Pacific Northwest (PNW) and Southeast (SEUS). The rise of OA in the SEUS is mainly driven by the enhanced formation of isoprene epoxydiols derived secondary organic aerosol due to the increase of isoprene and sulfate, while in the PNW, it is caused by wildfires. Ten climate models captured the OA increase in the PNW, yet greatly underestimated it in the SEUS.
Yuemeng Ji, Zhang Shi, Wenjian Li, Jiaxin Wang, Qiuju Shi, Yixin Li, Lei Gao, Ruize Ma, Weijun Lu, Lulu Xu, Yanpeng Gao, Guiying Li, and Taicheng An
Atmos. Chem. Phys., 24, 3079–3091, https://doi.org/10.5194/acp-24-3079-2024, https://doi.org/10.5194/acp-24-3079-2024, 2024
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The formation mechanisms for secondary brown carbon (SBrC) contributed by multifunctional reduced nitrogen compounds (RNCs) remain unclear. Hence, from combined laboratory experiments and quantum chemical calculations, we investigated the heterogeneous reactions of glyoxal (GL) with multifunctional RNCs, which are driven by four-step indirect nucleophilic addition reactions. Our results show a possible missing source for SBrC formation on urban, regional, and global scales.
Elyse A. Pennington, Yuan Wang, Benjamin C. Schulze, Karl M. Seltzer, Jiani Yang, Bin Zhao, Zhe Jiang, Hongru Shi, Melissa Venecek, Daniel Chau, Benjamin N. Murphy, Christopher M. Kenseth, Ryan X. Ward, Havala O. T. Pye, and John H. Seinfeld
Atmos. Chem. Phys., 24, 2345–2363, https://doi.org/10.5194/acp-24-2345-2024, https://doi.org/10.5194/acp-24-2345-2024, 2024
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To assess the air quality in Los Angeles (LA), we improved the CMAQ model by using dynamic traffic emissions and new secondary organic aerosol schemes to represent volatile chemical products. Source apportionment demonstrates that the urban areas of the LA Basin and vicinity are NOx-saturated, with the largest sensitivity of O3 to changes in volatile organic compounds in the urban core. The improvement and remaining issues shed light on the future direction of the model development.
Feifan Yan, Hang Su, Yafang Cheng, Rujin Huang, Hong Liao, Ting Yang, Yuanyuan Zhu, Shaoqing Zhang, Lifang Sheng, Wenbin Kou, Xinran Zeng, Shengnan Xiang, Xiaohong Yao, Huiwang Gao, and Yang Gao
Atmos. Chem. Phys., 24, 2365–2376, https://doi.org/10.5194/acp-24-2365-2024, https://doi.org/10.5194/acp-24-2365-2024, 2024
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PM2.5 pollution is a major air quality issue deteriorating human health, and previous studies mostly focus on regions like the North China Plain and Yangtze River Delta. However, the characteristics of PM2.5 concentrations between these two regions are studied less often. Focusing on the transport corridor region, we identify an interesting seesaw transport phenomenon with stagnant weather conditions, conducive to PM2.5 accumulation over this region, resulting in large health effects.
Prerita Agarwal, David S. Stevenson, and Mathew R. Heal
Atmos. Chem. Phys., 24, 2239–2266, https://doi.org/10.5194/acp-24-2239-2024, https://doi.org/10.5194/acp-24-2239-2024, 2024
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Air pollution levels across northern India are amongst some of the worst in the world, with episodic and hazardous haze events. Here, the ability of the WRF-Chem model to predict air quality over northern India is assessed against several datasets. Whilst surface wind speed and particle pollution peaks are over- and underestimated, respectively, meteorology and aerosol trends are adequately captured, and we conclude it is suitable for investigating severe particle pollution events.
George Jordan, Florent Malavelle, Ying Chen, Amy Peace, Eliza Duncan, Daniel G. Partridge, Paul Kim, Duncan Watson-Parris, Toshihiko Takemura, David Neubauer, Gunnar Myhre, Ragnhild Skeie, Anton Laakso, and James Haywood
Atmos. Chem. Phys., 24, 1939–1960, https://doi.org/10.5194/acp-24-1939-2024, https://doi.org/10.5194/acp-24-1939-2024, 2024
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The 2014–15 Holuhraun eruption caused a huge aerosol plume in an otherwise unpolluted region, providing a chance to study how aerosol alters cloud properties. This two-part study uses observations and models to quantify this relationship’s impact on the Earth’s energy budget. Part 1 suggests the models capture the observed spatial and chemical evolution of the plume, yet no model plume is exact. Understanding these differences is key for Part 2, where changes to cloud properties are explored.
Lin Du, Xiaofan Lv, Makroni Lily, Kun Li, and Narcisse Tsona Tchinda
Atmos. Chem. Phys., 24, 1841–1853, https://doi.org/10.5194/acp-24-1841-2024, https://doi.org/10.5194/acp-24-1841-2024, 2024
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This study explores the pH effect on the reaction of dissolved SO2 with selected organic peroxides. Results show that the formation of organic and/or inorganic sulfate from these peroxides strongly depends on their electronic structures, and these processes are likely to alter the chemical composition of dissolved organic matter in different ways. The rate constants of these reactions exhibit positive pH and temperature dependencies within pH 1–10 and 240–340 K ranges.
Angelo Riccio and Elena Chianese
Atmos. Chem. Phys., 24, 1673–1689, https://doi.org/10.5194/acp-24-1673-2024, https://doi.org/10.5194/acp-24-1673-2024, 2024
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Starting from the Copernicus Atmosphere Monitoring Service (CAMS), we provided a novel ensemble statistical post-processing approach to improve their air quality predictions. Our approach is able to provide reliable short-term forecasts of pollutant concentrations, which is a key challenge in supporting national authorities in their tasks related to EU Air Quality Directives, such as planning and reporting the state of air quality to the citizens.
Stella E. I. Manavi and Spyros N. Pandis
Atmos. Chem. Phys., 24, 891–909, https://doi.org/10.5194/acp-24-891-2024, https://doi.org/10.5194/acp-24-891-2024, 2024
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Organic vapors of intermediate volatility have often been neglected as sources of atmospheric organic aerosol. In this work we use a new approach for their simulation and quantify the contribution of these compounds emitted by transportation sources (gasoline and diesel vehicles) to particulate matter over Europe. The estimated secondary organic aerosol levels are on average 60 % higher than predicted by previous approaches. However, these estimates are probably lower limits.
Shenglan Jiang, Yan Zhang, Guangyuan Yu, Zimin Han, Junri Zhao, Tianle Zhang, and Mei Zheng
EGUsphere, https://doi.org/10.5194/egusphere-2024-155, https://doi.org/10.5194/egusphere-2024-155, 2024
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This study aims to provide gridded data on sea-wide concentrations, deposition fluxes, and soluble deposition fluxes with detailed source categories of metals by the modified CMAQ model. We developed a monthly emission inventory of six metals – Fe, Al, V, Ni, Zn, and Cu – from land anthropogenic, ship, and dust sources in East Asia in 2017. Our results revealed the contribution of each source to the emissions, concentrations, and deposition fluxes of metals in the East Asian seas.
Zhiyuan Li, Kin-Fai Ho, Harry Fung Lee, and Steve Hung Lam Yim
Atmos. Chem. Phys., 24, 649–661, https://doi.org/10.5194/acp-24-649-2024, https://doi.org/10.5194/acp-24-649-2024, 2024
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This study developed an integrated model framework for accurate multi-air-pollutant exposure assessments in high-density and high-rise cities. Following the proposed integrated model framework, we established multi-air-pollutant exposure models for four major PM10 chemical species as well as four criteria air pollutants with R2 values ranging from 0.73 to 0.93. The proposed framework serves as an important tool for combined exposure assessment in epidemiological studies.
Yujin Jo, Myoseon Jang, Sanghee Han, Azad Madhu, Bonyoung Koo, Yiqin Jia, Zechen Yu, Soontae Kim, and Jinsoo Park
Atmos. Chem. Phys., 24, 487–508, https://doi.org/10.5194/acp-24-487-2024, https://doi.org/10.5194/acp-24-487-2024, 2024
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The CAMx–UNIPAR model simulated the SOA budget formed via multiphase reactions of hydrocarbons and the impact of emissions and climate on SOA characteristics under California’s urban environments during winter 2018. SOA growth was dominated by daytime oxidation of long-chain alkanes and nighttime terpene oxidation with O3 and NO−3 radicals. The spatial distributions of anthropogenic SOA were affected by the northwesterly wind, whereas those of biogenic SOA were insensitive to wind directions.
Peter Huszar, Alvaro Patricio Prieto Perez, Lukáš Bartík, Jan Karlický, and Anahi Villalba-Pradas
Atmos. Chem. Phys., 24, 397–425, https://doi.org/10.5194/acp-24-397-2024, https://doi.org/10.5194/acp-24-397-2024, 2024
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Urbanization transforms rural land into artificial land, while due to human activities, it also introduces a great quantity of emissions. We quantify the impact of urbanization on the final particulate matter pollutant levels by looking not only at these emissions, but also at the way urban land cover influences meteorological conditions, how the removal of pollutants changes due to urban land cover, and how biogenic emissions from vegetation change due to less vegetation in urban areas.
Yinbao Jin, Yiming Liu, Xiao Lu, Xiaoyang Chen, Ao Shen, Haofan Wang, Yinping Cui, Yifei Xu, Siting Li, Jian Liu, Ming Zhang, Yingying Ma, and Qi Fan
Atmos. Chem. Phys., 24, 367–395, https://doi.org/10.5194/acp-24-367-2024, https://doi.org/10.5194/acp-24-367-2024, 2024
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This study aims to address these issues by evaluating eight independent biomass burning (BB) emission inventories (GFED, FINN1.5, FINN2.5 MOS, FINN2.5 MOSVIS, GFAS, FEER, QFED, and IS4FIRES) using the WRF-Chem model and analyzing their impact on aerosol optical properties (AOPs) and direct radiative forcing (DRF) during wildfire events in peninsular Southeast Asia (PSEA) that occurred in March 2019.
Hamza Ahsan, Hailong Wang, Jingbo Wu, Mingxuan Wu, Steven J. Smith, Susanne Bauer, Harrison Suchyta, Dirk Olivié, Gunnar Myhre, Hitoshi Matsui, Huisheng Bian, Jean-François Lamarque, Ken Carslaw, Larry Horowitz, Leighton Regayre, Mian Chin, Michael Schulz, Ragnhild Bieltvedt Skeie, Toshihiko Takemura, and Vaishali Naik
Atmos. Chem. Phys., 23, 14779–14799, https://doi.org/10.5194/acp-23-14779-2023, https://doi.org/10.5194/acp-23-14779-2023, 2023
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We examine the impact of the assumed effective height of SO2 injection, SO2 and BC emission seasonality, and the assumed fraction of SO2 emissions injected as SO4 on climate and chemistry model results. We find that the SO2 injection height has a large impact on surface SO2 concentrations and, in some models, radiative flux. These assumptions are a
hiddensource of inter-model variability and may be leading to bias in some climate model results.
Zhen Peng, Lili Lei, Zhe-Min Tan, Meigen Zhang, Aijun Ding, and Xingxia Kou
Atmos. Chem. Phys., 23, 14505–14520, https://doi.org/10.5194/acp-23-14505-2023, https://doi.org/10.5194/acp-23-14505-2023, 2023
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Annual PM2.5 emissions in China consistently decreased by about 3% to 5% from 2017 to 2020 with spatial variations and seasonal dependencies. High-temporal-resolution and dynamics-based PM2.5 emission estimates provide quantitative diurnal variations for each season. Significant reductions in PM2.5 emissions in the North China Plain and northeast of China in 2020 were caused by COVID-19.
Stylianos Kakavas, Spyros N. Pandis, and Athanasios Nenes
Atmos. Chem. Phys., 23, 13555–13564, https://doi.org/10.5194/acp-23-13555-2023, https://doi.org/10.5194/acp-23-13555-2023, 2023
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Water uptake from organic species in aerosol can affect the partitioning of semi-volatile inorganic compounds but are not considered in global and chemical transport models. We address this with a version of the PM-CAMx model that considers such organic water effects and use it to carry out 1-year aerosol simulations over the continental US. We show that such organic water impacts can increase dry PM1 levels by up to 2 μg m-3 when RH levels and PM1 concentrations are high.
Benjamin N. Murphy, Darrell Sonntag, Karl M. Seltzer, Havala O. T. Pye, Christine Allen, Evan Murray, Claudia Toro, Drew R. Gentner, Cheng Huang, Shantanu Jathar, Li Li, Andrew A. May, and Allen L. Robinson
Atmos. Chem. Phys., 23, 13469–13483, https://doi.org/10.5194/acp-23-13469-2023, https://doi.org/10.5194/acp-23-13469-2023, 2023
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We update methods for calculating organic particle and vapor emissions from mobile sources in the USA. Conventionally, particulate matter (PM) and volatile organic carbon (VOC) are speciated without consideration of primary semivolatile emissions. Our methods integrate state-of-the-science speciation profiles and correct for common artifacts when sampling emissions in a laboratory. We quantify impacts of the emission updates on ambient pollution with the Community Multiscale Air Quality model.
Yanshun Li, Randall V. Martin, Chi Li, Brian L. Boys, Aaron van Donkelaar, Jun Meng, and Jeffrey R. Pierce
Atmos. Chem. Phys., 23, 12525–12543, https://doi.org/10.5194/acp-23-12525-2023, https://doi.org/10.5194/acp-23-12525-2023, 2023
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We developed and evaluated processes affecting within-day (diel) variability in PM2.5 concentrations in a chemical transport model over the contiguous US. Diel variability in PM2.5 for the contiguous US is driven by early-morning accumulation into a shallow mixed layer, decreases from mid-morning through afternoon with mixed-layer growth, increases from mid-afternoon through evening as the mixed-layer collapses, and decreases overnight as emissions decrease.
Chupeng Zhang, Shangfei Hai, Yang Gao, Yuhang Wang, Shaoqing Zhang, Lifang Sheng, Bin Zhao, Shuxiao Wang, Jingkun Jiang, Xin Huang, Xiaojing Shen, Junying Sun, Aura Lupascu, Manish Shrivastava, Jerome D. Fast, Wenxuan Cheng, Xiuwen Guo, Ming Chu, Nan Ma, Juan Hong, Qiaoqiao Wang, Xiaohong Yao, and Huiwang Gao
Atmos. Chem. Phys., 23, 10713–10730, https://doi.org/10.5194/acp-23-10713-2023, https://doi.org/10.5194/acp-23-10713-2023, 2023
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New particle formation is an important source of atmospheric particles, exerting critical influences on global climate. Numerical models are vital tools to understanding atmospheric particle evolution, which, however, suffer from large biases in simulating particle numbers. Here we improve the model chemical processes governing particle sizes and compositions. The improved model reveals substantial contributions of newly formed particles to climate through effects on cloud condensation nuclei.
Xiaodong Xie, Jianlin Hu, Momei Qin, Song Guo, Min Hu, Dongsheng Ji, Hongli Wang, Shengrong Lou, Cheng Huang, Chong Liu, Hongliang Zhang, Qi Ying, Hong Liao, and Yuanhang Zhang
Atmos. Chem. Phys., 23, 10563–10578, https://doi.org/10.5194/acp-23-10563-2023, https://doi.org/10.5194/acp-23-10563-2023, 2023
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The atmospheric age of particles reflects how long particles have been formed and suspended in the atmosphere, which is closely associated with the evolution processes of particles. An analysis of the atmospheric age of PM2.5 provides a unique perspective on the evolution processes of different PM2.5 components. The results also shed lights on how to design effective emission control actions under unfavorable meteorological conditions.
Lea Fink, Matthias Karl, Volker Matthias, Sonia Oppo, Richard Kranenburg, Jeroen Kuenen, Sara Jutterström, Jana Moldanova, Elisa Majamäki, and Jukka-Pekka Jalkanen
Atmos. Chem. Phys., 23, 10163–10189, https://doi.org/10.5194/acp-23-10163-2023, https://doi.org/10.5194/acp-23-10163-2023, 2023
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The Mediterranean Sea is a heavily trafficked shipping area, and air quality monitoring stations in numerous cities along the Mediterranean coast have detected high levels of air pollutants originating from shipping emissions. The current study investigates how existing restrictions on shipping-related emissions to the atmosphere ensure compliance with legislation. Focus was laid on fine particles and particle species, which were simulated with five different chemical transport models.
Noah A. Stanton and Neil F. Tandon
Atmos. Chem. Phys., 23, 9191–9216, https://doi.org/10.5194/acp-23-9191-2023, https://doi.org/10.5194/acp-23-9191-2023, 2023
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Chemistry in Earth’s atmosphere has a potentially strong but very uncertain impact on climate. Past attempts to fully model chemistry in Earth’s troposphere (the lowest layer of the atmosphere) typically simplified the representation of Earth’s surface, which in turn limited the ability to simulate changes in climate. The cutting-edge model that we use in this study does not require such simplification, and we use it to examine the climate effects of chemical interactions in the troposphere.
Yiqi Zheng, Larry W. Horowitz, Raymond Menzel, David J. Paynter, Vaishali Naik, Jingyi Li, and Jingqiu Mao
Atmos. Chem. Phys., 23, 8993–9007, https://doi.org/10.5194/acp-23-8993-2023, https://doi.org/10.5194/acp-23-8993-2023, 2023
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Biogenic secondary organic aerosols (SOAs) account for a large fraction of fine aerosol at the global scale. Using long-term measurements and a climate model, we investigate anthropogenic impacts on biogenic SOA at both decadal and centennial timescales. Results show that despite reductions in biogenic precursor emissions, SOA has been strongly amplified by anthropogenic emissions since the preindustrial era and exerts a cooling radiative forcing.
Yuyang Li, Jiewen Shen, Bin Zhao, Runlong Cai, Shuxiao Wang, Yang Gao, Manish Shrivastava, Da Gao, Jun Zheng, Markku Kulmala, and Jingkun Jiang
Atmos. Chem. Phys., 23, 8789–8804, https://doi.org/10.5194/acp-23-8789-2023, https://doi.org/10.5194/acp-23-8789-2023, 2023
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We set up a new parameterization for 1.4 nm particle formation rates from sulfuric acid–dimethylamine (SA–DMA) nucleation, fully including the effects of coagulation scavenging and cluster stability. Incorporating the new parameterization into 3-D chemical transport models, we achieved better consistencies between simulation results and observation data. This new parameterization provides new insights into atmospheric nucleation simulations and its effects on atmospheric pollution or health.
María Gonçalves Ageitos, Vincenzo Obiso, Ron L. Miller, Oriol Jorba, Martina Klose, Matt Dawson, Yves Balkanski, Jan Perlwitz, Sara Basart, Enza Di Tomaso, Jerónimo Escribano, Francesca Macchia, Gilbert Montané, Natalie M. Mahowald, Robert O. Green, David R. Thompson, and Carlos Pérez García-Pando
Atmos. Chem. Phys., 23, 8623–8657, https://doi.org/10.5194/acp-23-8623-2023, https://doi.org/10.5194/acp-23-8623-2023, 2023
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Dust aerosols affect our climate differently depending on their mineral composition. We include dust mineralogy in an atmospheric model considering two existing soil maps, which still have large associated uncertainties. The soil data and the distribution of the minerals in different aerosol sizes are key to our model performance. We find significant regional variations in climate-relevant variables, which supports including mineralogy in our current models and the need for improved soil maps.
Jianyan Lu, Sunling Gong, Jian Zhang, Jianmin Chen, Lei Zhang, and Chunhong Zhou
Atmos. Chem. Phys., 23, 8021–8037, https://doi.org/10.5194/acp-23-8021-2023, https://doi.org/10.5194/acp-23-8021-2023, 2023
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WRF/CUACE was used to assess the cloud chemistry contribution in China. Firstly, the CUACE cloud chemistry scheme was found to reproduce well the cloud processing and consumption of H2O2, O3, and SO2, as well as the increase of sulfate. Secondly, during cloud availability in December under a heavy pollution episode, sulfate production increased 60–95 % and SO2 was reduced by over 80 %. This study provides a way to analyze the phenomenon of overestimation of SO2 in many chemical transport models.
Laurent Menut, Arineh Cholakian, Guillaume Siour, Rémy Lapere, Romain Pennel, Sylvain Mailler, and Bertrand Bessagnet
Atmos. Chem. Phys., 23, 7281–7296, https://doi.org/10.5194/acp-23-7281-2023, https://doi.org/10.5194/acp-23-7281-2023, 2023
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This study is about the wildfires occurring in France during the summer 2022. We study the forest fires that took place in the Landes during the summer of 2022. We show the direct impact of these fires on the air quality, especially downstream of the smoke plume towards the Paris region. We quantify the impact of these fires on the pollutants peak concentrations and the possible exceedance of thresholds.
Hannah J. Rubin, Joshua S. Fu, Frank Dentener, Rui Li, Kan Huang, and Hongbo Fu
Atmos. Chem. Phys., 23, 7091–7102, https://doi.org/10.5194/acp-23-7091-2023, https://doi.org/10.5194/acp-23-7091-2023, 2023
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We update the 2010 global deposition budget for nitrogen (N) and sulfur (S) with new regional wet deposition measurements, improving the ensemble results of 11 global chemistry transport models from HTAP II. Our study demonstrates that a global measurement–model fusion approach can substantially improve N and S deposition model estimates at a regional scale and represents a step forward toward the WMO goal of global fusion products for accurately mapping harmful air pollution.
Chenxi Li, Yuyang Li, Xiaoxiao Li, Runlong Cai, Yaxin Fan, Xiaohui Qiao, Rujing Yin, Chao Yan, Yishuo Guo, Yongchun Liu, Jun Zheng, Veli-Matti Kerminen, Markku Kulmala, Huayun Xiao, and Jingkun Jiang
Atmos. Chem. Phys., 23, 6879–6896, https://doi.org/10.5194/acp-23-6879-2023, https://doi.org/10.5194/acp-23-6879-2023, 2023
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New particle formation and growth in polluted environments are not fully understood despite intensive research. We applied a cluster dynamics–multicomponent sectional model to simulate the new particle formation events observed in Beijing, China. The simulation approximately captures how the events evolve. Further diagnosis shows that the oxygenated organic molecules may have been under-detected, and modulating their abundance leads to significantly improved simulation–observation agreement.
Marianne Tronstad Lund, Gunnar Myhre, Ragnhild Bieltvedt Skeie, Bjørn Hallvard Samset, and Zbigniew Klimont
Atmos. Chem. Phys., 23, 6647–6662, https://doi.org/10.5194/acp-23-6647-2023, https://doi.org/10.5194/acp-23-6647-2023, 2023
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Here we show that differences, in magnitude and trend, between recent global anthropogenic emission inventories have a notable influence on simulated regional abundances of anthropogenic aerosol over the 1990–2019 period. This, in turn, affects estimates of radiative forcing. Our findings form a basis for comparing existing and upcoming studies on anthropogenic aerosols using different emission inventories.
Lei Kong, Xiao Tang, Jiang Zhu, Zifa Wang, Yele Sun, Pingqing Fu, Meng Gao, Huangjian Wu, Miaomiao Lu, Qian Wu, Shuyuan Huang, Wenxuan Sui, Jie Li, Xiaole Pan, Lin Wu, Hajime Akimoto, and Gregory R. Carmichael
Atmos. Chem. Phys., 23, 6217–6240, https://doi.org/10.5194/acp-23-6217-2023, https://doi.org/10.5194/acp-23-6217-2023, 2023
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A multi-air-pollutant inversion system has been developed in this study to estimate emission changes in China during COVID-19 lockdown. The results demonstrate that the lockdown is largely a nationwide road traffic control measure with NOx emissions decreasing by ~40 %. Emissions of other species only decreased by ~10 % due to smaller effects of lockdown on other sectors. Assessment results further indicate that the lockdown only had limited effects on the control of PM2.5 and O3 in China.
Cited articles
Aiken, A. C., DeCarlo, P. F., Kroll, J. H., Worsnop, D. R., Huffman, J. A.,
Docherty, K. S., Ulbrich, I. M., Mohr, C., Kimmel, J. R., and Sueper, D.:
O ∕ C and OM ∕ OC ratios of primary, secondary, and ambient organic
aerosols with high-resolution time-of-flight aerosol mass spectrometry,
Environ. Sci. Technol., 42, 4478–4485, 2008.
Akagi, S. K., Yokelson, R. J., Wiedinmyer, C., Alvarado, M. J., Reid, J. S.,
Karl, T., Crounse, J. D., and Wennberg, P. O.: Emission factors for open and
domestic biomass burning for use in atmospheric models, Atmos. Chem. Phys.,
11, 4039–4072, https://doi.org/10.5194/acp-11-4039-2011, 2011.
Alexander, D. T. L., Crozier, P. A., and Anderson, J. R.: Brown carbon
spheres in East Asian outflow and their optical properties, Science, 321,
833–836, https://doi.org/10.1126/science.1155296, 2008.
Andreae, M. O. and Gelencsér, A.: Black carbon or brown carbon? The
nature of light-absorbing carbonaceous aerosols, Atmos. Chem. Phys., 6,
3131–3148, https://doi.org/10.5194/acp-6-3131-2006, 2006.
Andreae, M. O. and Merlet, P.: Emission of trace gases and aerosols from
biomass burning, Global Biogeochem. Cy., 15, 955–966, 2001.
Bahadur, R., Praveen, P. S., Xu, Y., and Ramanathan, V.: Solar absorption by
elemental and brown carbon determined from spectral observations, P. Natl.
Acad. Sci., 109, 17366–17371, 2012.
Bey, I., Jacob, D. J., Yantosca, R. M., and Logan, J. A.: Global modeling of
tropospheric chemistry with assimilated meteorology – Model description and
evaluation, J. Geophys. Res., 106, 23073–23095, 2001.
Bond, T. C. and Bergstrom, R. W.: Light absorption by carbonaceous particles:
An investigative review, Aerosol Sci. Tech., 40, 27–67, 2006.
Bond, T. C., Streets, D. G., Yarber, K. F., Nelson, S. M., Woo, J. H., and
Klimont, Z.: A technology-based global inventory of black and organic carbon
emissions from combustion, J. Geophys. Res., 109, D14203,
https://doi.org/10.1029/2003JD003697, 2004.
Bond, T. C., Habib, G., and Bergstrom, R. W.: Limitations in the enhancement
of visible light absorption due to mixing state, J. Geophys. Res, 111,
D20211, https://doi.org/10.1029/2006JD007315, 2006.
Bond, T. C., Bhardwaj, E., Dong, R., Jogani, R., Jung, S., Roden, C.,
Streets, D. G., and Trautmann, N. M.: Historical emissions of black and
organic carbon aerosol from energy-related combustion, 1850–2000, Global
Biogeochem. Cy., 21, GB2018, https://doi.org/10.1029/2006GB002840, 2007.
Bond, T. C., Doherty, S. J., Fahey, D. W., Forster, P. M., Berntsen, T.,
DeAngelo, B. J., Flanner, M. G., Ghan, S., Kärcher, B., Koch, D., Kinne,
S., Kondo, Y., Quinn, P. K., Sarofim, M. C., Schultz, M. G., Schulz, M.,
Venkataraman, C., Zhang, H., Zhang, S., Bellouin, N., Guttikunda, S. K.,
Hopke, P. K., Jacobson, M. Z., Kaiser, J. W., Klimont, Z., Lohmann, U.,
Schwarz, J. P., Shindell, D., Storelvmo, T., Warren, S. G., and Zender, C.
S.: Bounding the role of black carbon in the climate system: A scientific
assessment, J. Geophys. Res., 118, 5380–5552, https://doi.org/10.1002/jgrd.50171, 2013.
Bones, D. L., Henricksen, D. K., Mang, S. A., Gonsior, M., Bateman, A. P.,
Nguyen, T. B., Cooper, W. J., and Nizkorodov, S. A.: Appearance of strong
absorbers and fluorophores in limonene-O3 secondary organic aerosol due to
NH4+-mediated chemical aging over long time scales, J. Geophys. Res.,
115, D05203, https://doi.org/10.1029/2009JD012864, 2010.
Chakrabarty, R. K., Moosmüller, H., Chen, L.-W. A., Lewis, K., Arnott, W.
P., Mazzoleni, C., Dubey, M. K., Wold, C. E., Hao, W. M., and Kreidenweis, S.
M.: Brown carbon in tar balls from smoldering biomass combustion, Atmos.
Chem. Phys., 10, 6363–6370, https://doi.org/10.5194/acp-10-6363-2010, 2010.
Chakrabarty, R. K., Pervez, S., Chow, J. C., Watson, J. G., Dewangan, S.,
Robles, J., and Tian, G.: Funeral pyres in South Asia: Brown carbon aerosol
emissions and climate impacts, Environ. Sci. Tech. Lett., 1, 44–48, 2014.
Cheng, Y., He, K.-B., Zheng, M., Duan, F.-K., Du, Z.-Y., Ma, Y.-L., Tan,
J.-H., Yang, F.-M., Liu, J.-M., Zhang, X.-L., Weber, R. J., Bergin, M. H.,
and Russell, A. G.: Mass absorption efficiency of elemental carbon and
water-soluble organic carbon in Beijing, China, Atmos. Chem. Phys., 11,
11497–11510, https://doi.org/10.5194/acp-11-11497-2011, 2011.
Chin, M., Diehl, T., Dubovik, O., Eck, T. F., Holben, B. N., Sinyuk, A., and
Streets, D. G.: Light absorption by pollution, dust, and biomass burning
aerosols: a global model study and evaluation with AERONET measurements, Ann.
Geophys., 27, 3439–3464, https://doi.org/10.5194/angeo-27-3439-2009, 2009.
Chung, C. E., Kim, S.-W., Lee, M., Yoon, S.-C., and Lee, S.: Carbonaceous
aerosol AAE inferred from in-situ aerosol measurements at the Gosan ABC super
site, and the implications for brown carbon aerosol, Atmos. Chem. Phys., 12,
6173–6184, https://doi.org/10.5194/acp-12-6173-2012, 2012.
Chung, S. and Seinfeld, J.: Global distribution and climate forcing of
carbonaceous aerosols, J. Geophys. Res., 107, 4407,
https://doi.org/10.1029/2001JD001397, 2002.
Clarke, A., McNaughton, C., Kapustin, V., Shinozuka, Y., Howell, S., Dibb,
J., Zhou, J., Anderson, B., Brekhovskikh, V., and Turner, H.: Biomass burning
and pollution aerosol over North America: Organic components and their
influence on spectral optical properties and humidification response, J.
Geophys. Res., 112, D12S18, https://doi.org/10.1029/2006JD007777, 2007.
Cohen, J. B. and Wang, C.: Estimating global black carbon emissions using a
top-down Kalman Filter approach, J. Geophys. Res.-Atmos., 119, 307–323,
2014.
Cooke, W., Liousse, C., Cachier, H., and Feichter, J.: Construction of a
1 × 1 fossil fuel emission data set for carbonaceous aerosol and
implementation and radiative impact in the ECHAM4 model, J. Geophys. Res.,
104, 22137–22162, 1999.
Curci, G., Hogrefe, C., Bianconi, R., Im, U., Balzarini, A., Baró, R.,
Brunner, D., Forkel, R., Giordano, L., Hirtl, M., Honzak, L.,
Jiménez-Guerrero, P., Knote, C., Langer, M., Makar, P. A., Pirovano, G.,
Pérez, J. L., San José, R., Syrakov, D., Tuccella, P., Werhahn, J.,
Wolke, R., Žabkar, R., Zhang, J., and Galmarini, S.: Uncertainties of
simulated aerosol optical properties induced by assumptions on aerosol
physical and chemical properties: An AQMEII-2 perspective, Atmos. Environ.,
115, 541–552, 2015.
Diehl, T., Heil, A., Chin, M., Pan, X., Streets, D., Schultz, M., and Kinne,
S.: Anthropogenic, biomass burning, and volcanic emissions of black carbon,
organic carbon, and SO2 from 1980 to 2010 for hindcast model experiments,
Atmos. Chem. Phys. Discuss., 12, 24895–24954,
https://doi.org/10.5194/acpd-12-24895-2012, 2012.
Favez, O., Alfaro, S. C., Sciare, J., Cachier, H., and Abdelwahab, M. M.:
Ambient measurements of light-absorption by agricultural waste burning
organic aerosols, J. Aerosol Sci., 40, 613–620, 2009.
Feng, Y., Ramanathan, V., and Kotamarthi, V. R.: Brown carbon: a significant
atmospheric absorber of solar radiation?, Atmos. Chem. Phys., 13, 8607–8621,
https://doi.org/10.5194/acp-13-8607-2013, 2013.
Fernandes, S. D., Trautmann, N. M., Streets, D. G., Roden, C. A., and Bond,
T. C.: Global biofuel use, 1850–2000, Global Biogeochem. Cy., 21, GB2019,
2007.
Flores, J. M., Washenfelder, R., Adler, G., Lee, H., Segev, L., Laskin, J.,
Laskin, A., Nizkorodov, S., Brown, S., and Rudich, Y.: Complex refractive
indices in the near-ultraviolet spectral region of biogenic secondary organic
aerosol aged with ammonia, Phys. Chem. Chem. Phys., 16, 10629–10642, 2014.
Forster, P. V., Ramaswamy, P., Artaxo, T., Berntsen, R., Betts, D. W., Fahey,
J., Haywood, J., Lean, D. C., Lowe, G., Myhre, J., Nganga, R., Prinn, G.,
Raga, M. S., and Dorland, R. V.: Changes in Atmospheric Constituents and in
Radiative Forcing., Cambridge University Press, United Kingdom and New York,
NY, USA, 2007.
Goldstein, A. H. and Galbally, I. E.: Known and unexplored organic
constituents in the earth's atmosphere, Environ. Sci. Technol., 41,
1514–1521, 2007.
Graber, E. R. and Rudich, Y.: Atmospheric HULIS: How humic-like are they? A
comprehensive and critical review, Atmos. Chem. Phys., 6, 729–753,
https://doi.org/10.5194/acp-6-729-2006, 2006.
Granier, C., Bessagnet, B., Bond, T., D'Angiola, A., Denier van der Gon, H.,
Frost, G. J., Heil, A., Kaiser, J. W., Kinne, S., and Klimont, Z.: Evolution
of anthropogenic and biomass burning emissions of air pollutants at global
and regional scales during the 1980–2010 period, Climatic Change, 109,
163–190, 2011.
Hawkins, L. N., Baril, M. J., Sedehi, N., Galloway, M. M., De Haan, D. O.,
Schill, G. P., and Tolbert, M. A.: Formation of Semisolid, Oligomerized
Aqueous SOA: Lab Simulations of Cloud Processing, Environ. Sci. Technol., 48,
2273–2280, 2014.
Heald, C. L., Ridley, D. A., Kroll, J. H., Barrett, S. R. H., Cady-Pereira,
K. E., Alvarado, M. J., and Holmes, C. D.: Contrasting the direct radiative
effect and direct radiative forcing of aerosols, Atmos. Chem. Phys., 14,
5513–5527, https://doi.org/10.5194/acp-14-5513-2014, 2014.
Hecobian, A., Zhang, X., Zheng, M., Frank, N., Edgerton, E. S., and Weber, R.
J.: Water-Soluble Organic Aerosol material and the light-absorption
characteristics of aqueous extracts measured over the Southeastern United
States, Atmos. Chem. Phys., 10, 5965–5977, https://doi.org/10.5194/acp-10-5965-2010,
2010.
Henze, D. K. and Seinfeld, J. H.: Global secondary organic aerosol from
isoprene oxidation, Geophys. Res. Lett., 33, L09812,
https://doi.org/10.1029/2006GL025976, 2006.
Henze, D. K., Seinfeld, J. H., Ng, N. L., Kroll, J. H., Fu, T.-M., Jacob, D.
J., and Heald, C. L.: Global modeling of secondary organic aerosol formation
from aromatic hydrocarbons: high- vs. low-yield pathways, Atmos. Chem. Phys.,
8, 2405–2420, https://doi.org/10.5194/acp-8-2405-2008, 2008.
Hoffer, A., Gelencsér, A., Guyon, P., Kiss, G., Schmid, O., Frank, G. P.,
Artaxo, P., and Andreae, M. O.: Optical properties of humic-like substances
(HULIS) in biomass-burning aerosols, Atmos. Chem. Phys., 6, 3563–3570,
https://doi.org/10.5194/acp-6-3563-2006, 2006.
Huang, Y., Wu, S., Dubey, M. K., and French, N. H. F.: Impact of aging
mechanism on model simulated carbonaceous aerosols, Atmos. Chem. Phys., 13,
6329–6343, https://doi.org/10.5194/acp-13-6329-2013, 2013.
Iacono, M. J., Delamere, J. S., Mlawer, E. J., Shephard, M. W., Clough, S.
A., and Collins, W. D.: Radiative forcing by long-lived greenhouse gases:
Calculations with the AER radiative transfer models, J. Geophys. Res., 113,
D13103, https://doi.org/10.1029/2008JD009944, 2008.
Jacobson, M. Z.: Isolating nitrated and aromatic aerosols and nitrated
aromatic gases as sources of ultraviolet light absorption, J. Geophys. Res.,
104, 3527–3542, 1999.
Jacobson, M. Z.: Global direct radiative forcing due to multicomponent
anthropogenic and natural aerosols, J. Geophys. Res., 106, 1551–1568, 2001.
Jaoui, M., Edney, E. O., Kleindienst, T. E., Lewandowski, M., Offenberg, J.
H., Surratt, J. D., and Seinfeld, J. H.: Formation of secondary organic
aerosol from irradiated alpha-pinene/toluene/NOx mixtures and the effect
of isoprene and sulfur dioxide, J. Geophys. Res., 113, D09303,
https://doi.org/10.1029/2007JD009426, 2008.
Jiang, X., Wiedinmyer, C., and Carlton, A. G.: Aerosols from fires: An
examination of the effects on ozone photochemistry in the Western United
States, Environ. Sci. Technol., 46, 11878–11886, 2012.
Jo, D., Park, R., Kim, M., and Spracklen, D.: Effects of chemical aging on
global secondary organic aerosol using the volatility basis set approach,
Atmos. Environ., 81, 230–244, 2013.
Kaufman, Y. J., Justice, C. O., Flynn, L. P., Kendall, J. D., Prins, E. M.,
Giglio, L., Ward, D. E., Menzel, W. P., and Setzer, A. W.: Potential global
fire monitoring from EOS-MODIS, J. Geophys. Res., 103, 32215–32238, 1998.
Kim, H. and Paulson, S. E.: Real refractive indices and volatility of
secondary organic aerosol generated from photooxidation and ozonolysis of
limonene, α-pinene and toluene, Atmos. Chem. Phys., 13, 7711–7723,
https://doi.org/10.5194/acp-13-7711-2013, 2013.
Kirchstetter, T. W. and Thatcher, T. L.: Contribution of organic carbon to
wood smoke particulate matter absorption of solar radiation, Atmos. Chem.
Phys., 12, 6067–6072, https://doi.org/10.5194/acp-12-6067-2012, 2012.
Kirchstetter, T. W., Novakov, T., and Hobbs, P. V.: Evidence that the
spectral dependence of light absorption by aerosols is affected by organic
carbon, J. Geophys. Res., 109, D21208, https://doi.org/10.1029/2004JD004999, 2004.
Lamarque, J.-F., Bond, T. C., Eyring, V., Granier, C., Heil, A., Klimont, Z.,
Lee, D., Liousse, C., Mieville, A., Owen, B., Schultz, M. G., Shindell, D.,
Smith, S. J., Stehfest, E., Van Aardenne, J., Cooper, O. R., Kainuma, M.,
Mahowald, N., McConnell, J. R., Naik, V., Riahi, K., and van Vuuren, D. P.:
Historical (1850–2000) gridded anthropogenic and biomass burning emissions
of reactive gases and aerosols: methodology and application, Atmos. Chem.
Phys., 10, 7017–7039, https://doi.org/10.5194/acp-10-7017-2010, 2010.
Lambe, A. T., Cappa, C. D., Massoli, P., Onasch, T., Forestieri, S. D.,
Martin, A. T., Cummings, M. J., Croasdale, D. R., Brune, B., and Worsnop, D.
R.: Relationship between oxidation level and optical properties of secondary
organic aerosol, Environ. Sci. Technol., 47, 6349–6357, 2013.
Laskin, A., Laskin, J., and Nizkorodov, S. A.: Chemistry of Atmospheric Brown
Carbon, Chem. Rev., 115, 4335–4382, 2015.
Laskin, J., Laskin, A., Roach, P. J., Slysz, G. W., Anderson, G. A.,
Nizkorodov, S. A., Bones, D. L., and Nguyen, L. Q.: High-resolution
desorption electrospray ionization mass spectrometry for chemical
characterization of organic aerosols, Anal. Chem., 82, 2048–2058, 2010.
Laskin, J., Laskin, A., Nizkorodov, S. A., Roach, P., Eckert, P., Gilles, M.
K., Wang, B., Lee, H. J., and Hu, Q.: Molecular Selectivity of Brown Carbon
Chromophores, Environ. Sci. Technol., 48, 12047–12055, 2014.
Liao, H., Henze, D., Seinfeld, J., Wu, S., and Mickley, L.: Biogenic
secondary organic aerosol over the United States: Comparison of
climatological simulations with observations, J. Geophys. Res., 112, D06201,
https://doi.org/10.1029/2006JD007813, 2007.
Lin, G., Penner, J. E., Flanner, M. G., Sillman, S., Xu, L., and Zhou, C.:
Radiative forcing of organic aerosol in the atmosphere and on snow: Effects
of SOA and brown carbon, J. Geophys. Res.-Atmos., 119, 7453–7476, 2014.
Lin, P., Liu, J., Shilling, J. E., Kathmann, S. M., Laskin, J., and Laskin,
A.: Molecular characterization of brown carbon (BrC) chromophores in
secondary organic aerosol generated from photo-oxidation of toluene, Phys.
Chem. Chem. Phys., 17, 23312–23325, https://doi.org/10.1039/c5cp02563j, 2015.
Liu, J., Scheuer, E., Dibb, J., Ziemba, L. D., Thornhill, K., Anderson, B.
E., Wisthaler, A., Mikoviny, T., Devi, J. J., and Bergin, M.: Brown carbon in
the continental troposphere, Geophys. Res. Lett., 41, 2191–2195, 2014.
Liu, S., Shilling, J. E., Song, C., Hiranuma, N., Zaveri, R. A., and Russell,
L. M.: Hydrolysis of organonitrate functional groups in aerosol particles,
Aerosol Sci. Technol. 46, 1359–1369, 2012.
Lukács, H., Gelencsér, A., Hammer, S., Puxbaum, H., Pio, C., Legrand,
M., Kasper-Giebl, A., Handler, M., Limbeck, A., and Simpson, D.: Seasonal
trends and possible sources of brown carbon based on 2-year aerosol
measurements at six sites in Europe, J. Geophys. Res., 112, D23S18,
https://doi.org/10.1029/2006JD008151, 2007.
Malm, W. C., Sisler, J. F., Huffman, D., Eldred, R. A., and Cahill, T. A.:
Spatial and seasonal trends in particle concentration and optical extinction
in the United States, J. Geophys. Res., 99, 1347–1370, 1994.
Martin, R. V., Jacob, D. J., Yantosca, R. M., Chin, M., and Ginoux, P.:
Global and regional decreases in tropospheric oxidants from photochemical
effects of aerosols, J. Geophys. Res., 108, 4097, https://doi.org/10.1029/2002JD002622,
2003.
McMeeking, G. R.: The Optical, Chemical, And Physical Properties Of Aerosols
And Gases Emitted By The Laboratory Combustion Of Wildland Fuels,
Dissertation, Department of Atmospheric Science, Colorado State University,
Fort Collins, Colorado
Fall 2008, available at: http://chem.atmos.colostate.edu/Thesis/McMeeking%20dissertation.pdf (last access: 14 March 2016), 2008.
Mischenko, M. I., Travis, L. D., and Lacis, A. A.: Scattering, Absorption,
and Emission of Light by Small Particles, Cambridge University Press, UK,
2002.
Moise, T., Flores, J. M., and Rudich, Y.: Optical Properties of Secondary
Organic Aerosols and Their Changes by Chemical Processes, Chem. Rev., 115,
4400–4439, 2015.
Murphy, B. N. and Pandis, S. N.: Exploring summertime organic aerosol
formation in the eastern United States using a regional-scale budget approach
and ambient measurements, J. Geophys. Res., 115, D24216,
https://doi.org/10.1029/2010JD014418, 2010.
Myhre, G., Samset, B. H., Schulz, M., Balkanski, Y., Bauer, S., Berntsen, T.
K., Bian, H., Bellouin, N., Chin, M., Diehl, T., Easter, R. C., Feichter, J.,
Ghan, S. J., Hauglustaine, D., Iversen, T., Kinne, S., Kirkevåg, A.,
Lamarque, J.-F., Lin, G., Liu, X., Lund, M. T., Luo, G., Ma, X., van Noije,
T., Penner, J. E., Rasch, P. J., Ruiz, A., Seland, Ø., Skeie, R. B.,
Stier, P., Takemura, T., Tsigaridis, K., Wang, P., Wang, Z., Xu, L., Yu, H.,
Yu, F., Yoon, J.-H., Zhang, K., Zhang, H., and Zhou, C.: Radiative forcing of
the direct aerosol effect from AeroCom Phase II simulations, Atmos. Chem.
Phys., 13, 1853–1877, https://doi.org/10.5194/acp-13-1853-2013, 2013.
Nakayama, T., Matsumi, Y., Sato, K., Imamura, T., Yamazaki, A., and Uchiyama,
A.: Laboratory studies on optical properties of secondary organic aerosols
generated during the photooxidation of toluene and the ozonolysis of
α-pinene, J. Geophys. Res., 115, D24204, https://doi.org/10.1029/2010JD014387,
2010.
Nakayama, T., Sato, K., Matsumi, Y., Imamura, T., Yamazaki, A., and Uchiyama,
A.: Wavelength and NOx dependent complex refractive index of SOAs
generated from the photooxidation of toluene, Atmos. Chem. Phys., 13,
531–545, https://doi.org/10.5194/acp-13-531-2013, 2013.
Nguyen, T. B., Lee, P. B., Updyke, K. M., Bones, D. L., Laskin, J., Laskin,
A., and Nizkorodov, S. A.: Formation of nitrogen-and sulfur-containing
light-absorbing compounds accelerated by evaporation of water from secondary
organic aerosols, J. Geophys. Res., 117, D01207, https://doi.org/10.1029/2011JD016944,
2012.
Park, R. J., Jacob, D. J., Chin, M., and Martin, R. V.: Sources of
carbonaceous aerosols over the United States and implications for natural
visibility, J. Geophys. Res., 108, 4355, https://doi.org/10.1029/2002JD003190, 2003.
Park, R. J., Jacob, D. J., Kumar, N., and Yantosca, R. M.: Regional
visibility statistics in the United States: Natural and transboundary
pollution influences, and implications for the Regional Haze Rule, Atmos.
Environ., 40, 5405–5423, 2006.
Park, R. J., Kim, M. J., Jeong, J. I., Youn, D., and Kim, S.: A contribution
of brown carbon aerosol to the aerosol light absorption and its radiative
forcing in East Asia, Atmos. Environ., 44, 1414–1421, 2010.
Reid, J. S., Koppmann, R., Eck, T. F., and Eleuterio, D. P.: A review of
biomass burning emissions part II: intensive physical properties of biomass
burning particles, Atmos. Chem. Phys., 5, 799–825,
https://doi.org/10.5194/acp-5-799-2005, 2005.
Rienecker, M. M., Suarez, M. J., Gelaro, R., Todling, R., Bacmeister, J.,
Liu, E., Bosilovich, M. G., Schubert, S. D., Takacs, L., and Kim, G.-K.:
MERRA: NASA's modern-era retrospective analysis for research and
applications, J. Climate, 24, 3624–3648, 2011.
Saleh, R., Robinson, E. S., Tkacik, D. S., Ahern, A. T., Liu, S., Aiken, A.
C., Sullivan, R. C., Presto, A. A., Dubey, M. K., and Yokelson, R. J.:
Brownness of organics in aerosols from biomass burning linked to their black
carbon content, Nat. Geosci., 7, 647–650, 2014.
Sareen, N., Moussa, S. G., and McNeill, V. F.: Photochemical Aging of
Light-Absorbing Secondary Organic Aerosol Material, J. Phys. Chem. A, 117,
2987–2996, 2013.
Schnaiter, M., Gimmler, M., Llamas, I., Linke, C., Jäger, C., and Mutschke,
H.: Strong spectral dependence of light absorption by organic carbon
particles formed by propane combustion, Atmos. Chem. Phys., 6, 2981–2990,
https://doi.org/10.5194/acp-6-2981-2006, 2006.
Srinivas, B. and Sarin, M.: Brown carbon in atmospheric outflow from the
Indo-Gangetic Plain: Mass absorption efficiency and temporal variability,
Atmos. Environ., 89, 835–843, 2014.
Turpin, B. J. and Lim, H. J.: Species contributions to PM2.5 mass
concentrations: Revisiting common assumptions for estimating organic mass,
Aerosol Sci. Tech., 35, 602–610, 2001.
Updyke, K. M., Nguyen, T. B., and Nizkorodov, S. A.: Formation of Brown
Carbon via Reactions of Ammonia with Secondary Organic Aerosols from Biogenic
and Anthropogenic Precursors, Atmos. Environ., 63, 22–31, 2012.
Wang, X., Heald, C. L., Ridley, D. A., Schwarz, J. P., Spackman, J. R.,
Perring, A. E., Coe, H., Liu, D., and Clarke, A. D.: Exploiting simultaneous
observational constraints on mass and absorption to estimate the global
direct radiative forcing of black carbon and brown carbon, Atmos. Chem.
Phys., 14, 10989–11010, https://doi.org/10.5194/acp-14-10989-2014, 2014.
Ward, D., Susott, R., Kauffman, J., Babbitt, R., Cummings, D., Dias, B.,
Holben, B., Kaufman, Y., Rasmussen, R., and Setzer, A.: Smoke and Fire
Characteristics for Cerrado and Deforestation Burns in Brazil: BASE-B
Experiment, Journal of Geophysical Research, 97, 14601-14619, 1992.
Ward, D. E. and Hao, W.: Projections of Emissions from Burning of Biomass
Foruse in Studies of Global Climate and Atmospheric Chemistry, Air and Waste
Management Association, Vancouver, British Colombia, Canada, 1991.
Weber, R. J., Sullivan, A. P., Peltier, R. E., Russell, A., Yan, B., Zheng,
M., de Gouw, J., Warneke, C., Brock, C., and Holloway, J. S.: A study of
secondary organic aerosol formation in the anthropogenic-influenced
southeastern United States, J. Geophys. Res., 112, D13302,
https://doi.org/10.1029/2007JD008408, 2007.
Wiedinmyer, C., Akagi, S. K., Yokelson, R. J., Emmons, L. K., Al-Saadi, J.
A., Orlando, J. J., and Soja, A. J.: The Fire INventory from NCAR (FINN): a
high resolution global model to estimate the emissions from open burning,
Geosci. Model Dev., 4, 625–641, https://doi.org/10.5194/gmd-4-625-2011, 2011.
Yang, M., Howell, S. G., Zhuang, J., and Huebert, B. J.: Attribution of
aerosol light absorption to black carbon, brown carbon, and dust in China –
interpretations of atmospheric measurements during EAST-AIRE, Atmos. Chem.
Phys., 9, 2035–2050, https://doi.org/10.5194/acp-9-2035-2009, 2009.
Yu, L., Smith, J., Laskin, A., Anastasio, C., Laskin, J., and Zhang, Q.:
Chemical characterization of SOA formed from aqueous-phase reactions of
phenols with the triplet excited state of carbonyl and hydroxyl radical,
Atmos. Chem. Phys., 14, 13801–13816, https://doi.org/10.5194/acp-14-13801-2014, 2014.
Zhang, X., Lin, Y. H., Surratt, J. D., Zotter, P., Prévôt, A. S. H.,
and Weber, R. J.: Light-absorbing soluble organic aerosol in Los Angeles and
Atlanta: A contrast in secondary organic aerosol, Geophys. Res. Lett., 38,
L21810, https://doi.org/10.1029/2011GL049385, 2011.
Zhang, X., Lin, Y.-H., Surratt, J. D., and Weber, R. J.: Sources, Composition
and Absorption Ångström Exponent of Light-absorbing Organic
Components in Aerosol Extracts from the Los Angeles Basin, Environ. Sci.
Technol., 47, 3685–3693, https://doi.org/10.1021/es305047b, 2013.
Zhong, M. and Jang, M.: Light absorption coefficient measurement of SOA using
a UV-Visible spectrometer connected with an integrating sphere, Atmos.
Environ., 45, 4263–4271, 2011.
Zhong, M., Jang, M., Oliferenko, A., Pillai, G. G., and Katritzky, A. R.: The
SOA Formation Model Combined with Semiempirical Quantum Chemistry to Predict
UV-Vis Absorption of Secondary Organic Aerosols, Phys. Chem. Chem. Phys., 14,
9058–9066, 2012.
Short summary
We develop a new approach to estimate global emission of primary brown carbon from biomass burning and biofuel use and explicitly simulate brown carbon aerosol that has not been considered in climate and air quality models despite of its importance for solar absorption at UV and short visible wavelengths. Using our best simulation results, we estimate radiative effects of brown carbon aerosol for climate and photochemistry.
We develop a new approach to estimate global emission of primary brown carbon from biomass...
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