Articles | Volume 21, issue 17
Atmos. Chem. Phys., 21, 13051–13065, 2021
https://doi.org/10.5194/acp-21-13051-2021
© Author(s) 2021. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Atmos. Chem. Phys., 21, 13051–13065, 2021
https://doi.org/10.5194/acp-21-13051-2021
© Author(s) 2021. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Research article 02 Sep 2021
Research article | 02 Sep 2021
Urban aerosol chemistry at a land–water transition site during summer – Part 1: Impact of agricultural and industrial ammonia emissions
Nicholas Balasus et al.
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Michael A. Battaglia Jr., Nicholas Balasus, Katherine Ball, Vanessa Caicedo, Ruben Delgado, Annmarie G. Carlton, and Christopher J. Hennigan
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2021-368, https://doi.org/10.5194/acp-2021-368, 2021
Revised manuscript under review for ACP
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This study characterizes aerosol liquid water content and aerosol pH at a land-water transition site near Baltimore, Maryland. We characterize the effects of unique meteorology associated with the close proximity to the Chesapeake Bay and episodic NH3 events emitted from industrial and agricultural sources on aerosol chemistry during the summer. We also examine two events where primary Bay emissions underwent ageing in the polluted urban atmosphere.
Jianfeng Li, Yuhang Wang, Ruixiong Zhang, Charles Smeltzer, Andrew Weinheimer, Jay Herman, K. Folkert Boersma, Edward A. Celarier, Russell W. Long, James J. Szykman, Ruben Delgado, Anne M. Thompson, Travis N. Knepp, Lok N. Lamsal, Scott J. Janz, Matthew G. Kowalewski, Xiong Liu, and Caroline R. Nowlan
Atmos. Chem. Phys., 21, 11133–11160, https://doi.org/10.5194/acp-21-11133-2021, https://doi.org/10.5194/acp-21-11133-2021, 2021
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Comprehensive evaluations of simulated diurnal cycles of NO2 and NOy concentrations, vertical profiles, and tropospheric vertical column densities at two different resolutions with various measurements during the DISCOVER-AQ 2011 campaign show potential distribution biases of NOx emissions in the National Emissions Inventory 2011 at both 36 and 4 km resolutions, providing another possible explanation for the overestimation of model results.
Michael A. Battaglia Jr., Nicholas Balasus, Katherine Ball, Vanessa Caicedo, Ruben Delgado, Annmarie G. Carlton, and Christopher J. Hennigan
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2021-368, https://doi.org/10.5194/acp-2021-368, 2021
Revised manuscript under review for ACP
Short summary
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This study characterizes aerosol liquid water content and aerosol pH at a land-water transition site near Baltimore, Maryland. We characterize the effects of unique meteorology associated with the close proximity to the Chesapeake Bay and episodic NH3 events emitted from industrial and agricultural sources on aerosol chemistry during the summer. We also examine two events where primary Bay emissions underwent ageing in the polluted urban atmosphere.
Amy E. Christiansen, Annmarie G. Carlton, and Barron H. Henderson
Atmos. Chem. Phys., 20, 11607–11624, https://doi.org/10.5194/acp-20-11607-2020, https://doi.org/10.5194/acp-20-11607-2020, 2020
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We quantify differences in surface-level fine particle mass (PM2.5) chemical composition in relation to satellite-derived cloud flags and find significant differences between clear-sky and cloud days. The work suggests that future analysis in this area is warranted.
Havala O. T. Pye, Athanasios Nenes, Becky Alexander, Andrew P. Ault, Mary C. Barth, Simon L. Clegg, Jeffrey L. Collett Jr., Kathleen M. Fahey, Christopher J. Hennigan, Hartmut Herrmann, Maria Kanakidou, James T. Kelly, I-Ting Ku, V. Faye McNeill, Nicole Riemer, Thomas Schaefer, Guoliang Shi, Andreas Tilgner, John T. Walker, Tao Wang, Rodney Weber, Jia Xing, Rahul A. Zaveri, and Andreas Zuend
Atmos. Chem. Phys., 20, 4809–4888, https://doi.org/10.5194/acp-20-4809-2020, https://doi.org/10.5194/acp-20-4809-2020, 2020
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Acid rain is recognized for its impacts on human health and ecosystems, and programs to mitigate these effects have had implications for atmospheric acidity. Historical measurements indicate that cloud and fog droplet acidity has changed in recent decades in response to controls on emissions from human activity, while the limited trend data for suspended particles indicate acidity may be relatively constant. This review synthesizes knowledge on the acidity of atmospheric particles and clouds.
Michael A. Battaglia Jr., Rodney J. Weber, Athanasios Nenes, and Christopher J. Hennigan
Atmos. Chem. Phys., 19, 14607–14620, https://doi.org/10.5194/acp-19-14607-2019, https://doi.org/10.5194/acp-19-14607-2019, 2019
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The effects of water-soluble organic carbon (WSOC) on aerosol pH were characterized for aqueous-phase particles containing a mixture of inorganics and organics. The ISORROPIA-II and E-AIM models were used in conjunction with AIOMFAC to quantify the effect of organics on aerosol pH through (1) changes to the aerosol liquid water content and (2) changes to the hydrogen ion activity coefficient. The study included both organic acids and nonacids, at RH levels ranging from 70 to 90 %.
Hayley S. Glicker, Michael J. Lawler, John Ortega, Suzane S. de Sá, Scot T. Martin, Paulo Artaxo, Oscar Vega Bustillos, Rodrigo de Souza, Julio Tota, Annmarie Carlton, and James N. Smith
Atmos. Chem. Phys., 19, 13053–13066, https://doi.org/10.5194/acp-19-13053-2019, https://doi.org/10.5194/acp-19-13053-2019, 2019
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An understanding of the chemical composition of the smallest particles in the air over the Amazon Basin provides insights into the natural and human-caused influences on particle production in this sensitive region. We present measurements of the composition of sub-100 nm diameter particles performed during the wet season and identify unique constituents that point to both natural and human-caused sources and processes.
Jingqiu Mao, Annmarie Carlton, Ronald C. Cohen, William H. Brune, Steven S. Brown, Glenn M. Wolfe, Jose L. Jimenez, Havala O. T. Pye, Nga Lee Ng, Lu Xu, V. Faye McNeill, Kostas Tsigaridis, Brian C. McDonald, Carsten Warneke, Alex Guenther, Matthew J. Alvarado, Joost de Gouw, Loretta J. Mickley, Eric M. Leibensperger, Rohit Mathur, Christopher G. Nolte, Robert W. Portmann, Nadine Unger, Mika Tosca, and Larry W. Horowitz
Atmos. Chem. Phys., 18, 2615–2651, https://doi.org/10.5194/acp-18-2615-2018, https://doi.org/10.5194/acp-18-2615-2018, 2018
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This paper is aimed at discussing progress in evaluating, diagnosing, and improving air quality and climate modeling using comparisons to SAS observations as a guide to thinking about improvements to mechanisms and parameterizations in models.
Marwa M. H. El-Sayed, Diana L. Ortiz-Montalvo, and Christopher J. Hennigan
Atmos. Chem. Phys., 18, 1171–1184, https://doi.org/10.5194/acp-18-1171-2018, https://doi.org/10.5194/acp-18-1171-2018, 2018
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We characterized the reversibility of aqSOA formed from isoprene at a location in the eastern United States. WSOCp evaporation with drying was observed systematically throughout the late spring and summer, indicating reversible aqSOA formation. The absolute reversible aqSOA concentrations, as well as the relative amount of reversible aqSOA, increased with decreasing NOx / isoprene ratios, suggesting that IEPOX or other low-NOx oxidation products were responsible for these effects.
Haihan Chen, Anna L. Hodshire, John Ortega, James Greenberg, Peter H. McMurry, Annmarie G. Carlton, Jeffrey R. Pierce, Dave R. Hanson, and James N. Smith
Atmos. Chem. Phys., 18, 311–326, https://doi.org/10.5194/acp-18-311-2018, https://doi.org/10.5194/acp-18-311-2018, 2018
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Much of what we know about atmospheric new particle formation (NPF) is based on ground-level measurements. We used tethered balloon measurements and remote sensing to study the location in the boundary layer in which NPF events are initiated, the degree to which the boundary layer is well-mixed during NPF, and the potential role that water may play in aerosol particle chemical evolution. This information will improve the representativeness of process level models and laboratory experiments.
Travis N. Knepp, James J. Szykman, Russell Long, Rachelle M. Duvall, Jonathan Krug, Melinda Beaver, Kevin Cavender, Keith Kronmiller, Michael Wheeler, Ruben Delgado, Raymond Hoff, Timothy Berkoff, Erik Olson, Richard Clark, Daniel Wolfe, David Van Gilst, and Doreen Neil
Atmos. Meas. Tech., 10, 3963–3983, https://doi.org/10.5194/amt-10-3963-2017, https://doi.org/10.5194/amt-10-3963-2017, 2017
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Herein we compare the mixed-layer data products from differing ceilometer instruments and meteorological sondes.
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
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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.
Laura Bianco, Katja Friedrich, James M. Wilczak, Duane Hazen, Daniel Wolfe, Ruben Delgado, Steven P. Oncley, and Julie K. Lundquist
Atmos. Meas. Tech., 10, 1707–1721, https://doi.org/10.5194/amt-10-1707-2017, https://doi.org/10.5194/amt-10-1707-2017, 2017
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XPIA is a study held in 2015 at NOAA's Boulder Atmospheric Observatory facility, aimed at assessing remote-sensing capabilities for wind energy applications. We use well-defined reference systems to validate temperature retrieved by two microwave radiometers (MWRs) and virtual temperature measured by wind profiling radars with radio acoustic sounding systems (RASSs). Water vapor density and relative humidity by the MWRs were also compared with similar measurements from the reference systems.
Vanessa Caicedo, Bernhard Rappenglück, Barry Lefer, Gary Morris, Daniel Toledo, and Ruben Delgado
Atmos. Meas. Tech., 10, 1609–1622, https://doi.org/10.5194/amt-10-1609-2017, https://doi.org/10.5194/amt-10-1609-2017, 2017
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Three methods for estimating the boundary layer height using aerosol backscatter measurements are evaluated here. Radiosonde profiles are used to evaluate aerosol-backscatter-derived boundary layer heights. Overall good agreement between radiosonde and all aerosol-derived boundary layer heights was found, and specific limitations to each method are discussed. A recommended method is given for future aerosol backscatter retrieval of the boundary layer height.
Kathleen M. Fahey, Annmarie G. Carlton, Havala O. T. Pye, Jaemeen Baek, William T. Hutzell, Charles O. Stanier, Kirk R. Baker, K. Wyat Appel, Mohammed Jaoui, and John H. Offenberg
Geosci. Model Dev., 10, 1587–1605, https://doi.org/10.5194/gmd-10-1587-2017, https://doi.org/10.5194/gmd-10-1587-2017, 2017
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Chemical transport models (CTMs) are a crucial tool in understanding links between emissions, air quality, and climate. Only a simple description of cloud chemistry has been implemented in many of these; however, clouds play a major role in the physicochemical processing of atmospheric species. In CMAQ, EPA’s widely used CTM, the cloud code is limited to the treatment of simple chemistry. We update CMAQ clouds to consider additional chemistry and then examine regional impacts of these updates.
Mithu Debnath, Giacomo Valerio Iungo, W. Alan Brewer, Aditya Choukulkar, Ruben Delgado, Scott Gunter, Julie K. Lundquist, John L. Schroeder, James M. Wilczak, and Daniel Wolfe
Atmos. Meas. Tech., 10, 1215–1227, https://doi.org/10.5194/amt-10-1215-2017, https://doi.org/10.5194/amt-10-1215-2017, 2017
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The XPIA experiment was conducted in 2015 at the Boulder Atmospheric Observatory to estimate capabilities of various remote-sensing techniques for the characterization of complex atmospheric flows. Among different tests, XPIA provided the unique opportunity to perform simultaneous virtual towers with Ka-band radars and scanning Doppler wind lidars. Wind speed and wind direction were assessed against lidar profilers and sonic anemometer data, highlighting a good accuracy of the data retrieved.
Mithu Debnath, G. Valerio Iungo, Ryan Ashton, W. Alan Brewer, Aditya Choukulkar, Ruben Delgado, Julie K. Lundquist, William J. Shaw, James M. Wilczak, and Daniel Wolfe
Atmos. Meas. Tech., 10, 431–444, https://doi.org/10.5194/amt-10-431-2017, https://doi.org/10.5194/amt-10-431-2017, 2017
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Triple RHI scans were performed with three simultaneous scanning Doppler wind lidars and assessed with lidar profiler and sonic anemometer data. This test is part of the XPIA experiment. The scan strategy consists in two lidars performing co-planar RHI scans, while a third lidar measures the transversal velocity component. The results show that horizontal velocity and wind direction are measured with good accuracy, while the vertical velocity is typically measured with a significant error.
Havala O. T. Pye, Benjamin N. Murphy, Lu Xu, Nga L. Ng, Annmarie G. Carlton, Hongyu Guo, Rodney Weber, Petros Vasilakos, K. Wyat Appel, Sri Hapsari Budisulistiorini, Jason D. Surratt, Athanasios Nenes, Weiwei Hu, Jose L. Jimenez, Gabriel Isaacman-VanWertz, Pawel K. Misztal, and Allen H. Goldstein
Atmos. Chem. Phys., 17, 343–369, https://doi.org/10.5194/acp-17-343-2017, https://doi.org/10.5194/acp-17-343-2017, 2017
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We use a chemical transport model to examine how organic compounds in the atmosphere interact with water present in particles. Organic compounds themselves lead to water uptake, and organic compounds interact with water associated with inorganic compounds in the rural southeast atmosphere. Including interactions of organic compounds with water requires a treatment of nonideality to more accurately represent aerosol observations during the Southern Oxidant and Aerosol Study (SOAS) 2013.
Neha Sareen, Annmarie G. Carlton, Jason D. Surratt, Avram Gold, Ben Lee, Felipe D. Lopez-Hilfiker, Claudia Mohr, Joel A. Thornton, Zhenfa Zhang, Yong B. Lim, and Barbara J. Turpin
Atmos. Chem. Phys., 16, 14409–14420, https://doi.org/10.5194/acp-16-14409-2016, https://doi.org/10.5194/acp-16-14409-2016, 2016
P. L. Hayes, A. G. Carlton, K. R. Baker, R. Ahmadov, R. A. Washenfelder, S. Alvarez, B. Rappenglück, J. B. Gilman, W. C. Kuster, J. A. de Gouw, P. Zotter, A. S. H. Prévôt, S. Szidat, T. E. Kleindienst, J. H. Offenberg, P. K. Ma, and J. L. Jimenez
Atmos. Chem. Phys., 15, 5773–5801, https://doi.org/10.5194/acp-15-5773-2015, https://doi.org/10.5194/acp-15-5773-2015, 2015
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(1) Four different parameterizations for the formation and chemical evolution of secondary organic aerosol (SOA) are evaluated using a box model representing the Los Angeles region during the CalNex campaign.
(2) The SOA formed only from the oxidation of VOCs is insufficient to explain the observed SOA concentrations.
(3) The amount of SOA mass formed from diesel vehicle emissions is estimated to be 16-27%.
(4) Modeled SOA depends strongly on the P-S/IVOC volatility distribution.
C. J. Hennigan, J. Izumi, A. P. Sullivan, R. J. Weber, and A. Nenes
Atmos. Chem. Phys., 15, 2775–2790, https://doi.org/10.5194/acp-15-2775-2015, https://doi.org/10.5194/acp-15-2775-2015, 2015
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We show that the ion balance and molar ratio methods are unsuitable for use as aerosol pH proxies. Our recommendation is that 1) thermodynamic equilibrium models constrained by both gas and aerosol inputs run in the forward (open) mode, and 2) the phase partitioning of ammonia provides the best predictions of aerosol pH. Given the significance of acidity for numerous chemical processes in the atmosphere, the implications of this study are important and far reaching.
K. C. Barsanti, A. G. Carlton, and S. H. Chung
Atmos. Chem. Phys., 13, 12073–12088, https://doi.org/10.5194/acp-13-12073-2013, https://doi.org/10.5194/acp-13-12073-2013, 2013
A. G. Carlton and B. J. Turpin
Atmos. Chem. Phys., 13, 10203–10214, https://doi.org/10.5194/acp-13-10203-2013, https://doi.org/10.5194/acp-13-10203-2013, 2013
R. Saleh, C. J. Hennigan, G. R. McMeeking, W. K. Chuang, E. S. Robinson, H. Coe, N. M. Donahue, and A. L. Robinson
Atmos. Chem. Phys., 13, 7683–7693, https://doi.org/10.5194/acp-13-7683-2013, https://doi.org/10.5194/acp-13-7683-2013, 2013
C. He, J. Liu, A. G. Carlton, S. Fan, L. W. Horowitz, H. Levy II, and S. Tao
Atmos. Chem. Phys., 13, 1913–1926, https://doi.org/10.5194/acp-13-1913-2013, https://doi.org/10.5194/acp-13-1913-2013, 2013
Related subject area
Subject: Aerosols | Research Activity: Field Measurements | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Ammonium nitrate promotes sulfate formation through uptake kinetic regime
Measurement report: Indirect evidence for the controlling influence of acidity on the speciation of iodine in Atlantic aerosols
Measurement report: Vertical distribution of biogenic and anthropogenic secondary organic aerosols in the urban boundary layer over Beijing during late summer
Source-specific light absorption by carbonaceous components in the complex aerosol matrix from yearly filter-based measurements
Variability in black carbon mass concentration in surface snow at Svalbard
Rapid mass growth and enhanced light extinction of atmospheric aerosols during the heating season haze episodes in Beijing revealed by aerosol–chemistry–radiation–boundary layer interaction
Measurement report: Saccharide composition in atmospheric fine particulate matter during spring at the remote sites of southwest China and estimates of source contributions
Gas–particle partitioning of polyol tracers at a suburban site in Nanjing, east China: increased partitioning to the particle phase
Measurement report: Source characteristics of water-soluble organic carbon in PM2.5 at two sites in Japan, as assessed by long-term observation and stable carbon isotope ratio
The importance of sesquiterpene oxidation products for secondary organic aerosol formation in a springtime hemiboreal forest
PM1 composition and source apportionment at two sites in Delhi, India, across multiple seasons
Increase of nitrooxy organosulfates in firework-related urban aerosols during Chinese New Year's Eve
Differentiation of coarse-mode anthropogenic, marine and dust particles in the High Arctic islands of Svalbard
Source apportionment of atmospheric PM10 oxidative potential: synthesis of 15 year-round urban datasets in France
Measurement report: Long-emission-wavelength chromophores dominate the light absorption of brown carbon in aerosols over Bangkok: impact from biomass burning
Secondary organic aerosols from anthropogenic volatile organic compounds contribute substantially to air pollution mortality
Dramatic changes in Harbin aerosol during 2018–2020: the roles of open burning policy and secondary aerosol formation
Mediterranean nascent sea spray organic aerosol and relationships with seawater biogeochemistry
Seasonal analysis of submicron aerosol in Old Delhi using high-resolution aerosol mass spectrometry: chemical characterisation, source apportionment and new marker identification
Eight years of sub-micrometre organic aerosol composition data from the boreal forest characterized using a machine-learning approach
Quantification of solid fuel combustion and aqueous chemistry contributions to secondary organic aerosol during wintertime haze events in Beijing
Large seasonal and interannual variations of biogenic sulfur compounds in the Arctic atmosphere (Svalbard; 78.9° N, 11.9° E)
Disparities in particulate matter (PM10) origins and oxidative potential at a city scale (Grenoble, France) – Part 2: Sources of PM10 oxidative potential using multiple linear regression analysis and the predictive applicability of multilayer perceptron neural network analysis
Inter-annual variations of wet deposition in Beijing from 2014–2017: implications of below-cloud scavenging of inorganic aerosols
Urban organic aerosol composition in eastern China differs from north to south: molecular insight from a liquid chromatography–mass spectrometry (Orbitrap) study
Cultivable halotolerant ice-nucleating bacteria and fungi in coastal precipitation
Determination of free amino acids, saccharides, and selected microbes in biogenic atmospheric aerosols – seasonal variations, particle size distribution, chemical and microbial relations
Physical and chemical properties of urban aerosols in São Paulo, Brazil: links between composition and size distribution of submicron particles
Substantial changes in gaseous pollutants and chemical compositions in fine particles in the North China Plain during the COVID-19 lockdown period: anthropogenic vs. meteorological influences
Measurement report: Spatiotemporal and policy-related variations of PM2.5 compositions and sources during 2015–2019 at multisite of a Chinese megacity
Measurement report: Molecular composition, optical properties, and radiative effects of water-soluble organic carbon in snowpack samples from northern Xinjiang, China
Reduced volatility of aerosols from surface emission to the top of planetary boundary layer
Significant contrasts in aerosol acidity between China and the United States
Increase in secondary organic aerosol in an urban environment
Carbonaceous aerosol composition in air masses influenced by large-scale biomass burning: a case study in northwestern Vietnam
The role of coarse aerosol particles as a sink of HNO3 in wintertime pollution events in the Salt Lake Valley
Molecular characterization of gaseous and particulate oxygenated compounds at a remote site in Cape Corsica in the western Mediterranean Basin
Aircraft measurements of aerosol and trace gas chemistry in the eastern North Atlantic
Impacts of the COVID-19 lockdown on air pollution at regional and urban background sites in northern Italy
Measurement report: Fourteen months of real-time characterisation of the submicronic aerosol and its atmospheric dynamics at the Marseille–Longchamp supersite
Trends, composition, and sources of carbonaceous aerosol at the Birkenes Observatory, northern Europe, 2001–2018
Enhancement of nanoparticle formation and growth during the COVID-19 lockdown period in urban Beijing
Chemical composition and source attribution of sub-micrometre aerosol particles in the summertime Arctic lower troposphere
Sources of black carbon at residential and traffic environments
In-depth characterization of submicron particulate matter inter-annual variations at a street canyon site in northern Europe
Measurement report: The chemical composition and temporal variability of aerosol particles at Tuktoyaktuk, Canada during the Year of Polar Prediction Special Observing Period
Measurement report: Firework impacts on air quality in Metro Manila, Philippines, during the 2019 New Year revelry
Measurement report: Receptor modelling for source identification of urban fine and coarse particulate matter using hourly elemental composition
Chemical composition of PM2.5 in October 2017 Northern California wildfire plumes
Atmospheric conditions and composition that influence PM2.5 oxidative potential in Beijing, China
Yongchun Liu, Zemin Feng, Feixue Zheng, Xiaolei Bao, Pengfei Liu, Yanli Ge, Yan Zhao, Tao Jiang, Yunwen Liao, Yusheng Zhang, Xiaolong Fan, Chao Yan, Biwu Chu, Yonghong Wang, Wei Du, Jing Cai, Federico Bianchi, Tuukka Petäjä, Yujing Mu, Hong He, and Markku Kulmala
Atmos. Chem. Phys., 21, 13269–13286, https://doi.org/10.5194/acp-21-13269-2021, https://doi.org/10.5194/acp-21-13269-2021, 2021
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The mechanisms and kinetics of particulate sulfate formation in the atmosphere are still open questions although they have been extensively discussed. We found that uptake of SO2 is the rate-determining step for the conversion of SO2 to particulate sulfate. NH4NO3 plays an important role in AWC, the phase state of aerosol particles, and subsequently the uptake kinetics of SO2 under high-RH conditions. This work is a good example of the feedback between aerosol physics and aerosol chemistry.
Alex R. Baker and Chan Yodle
Atmos. Chem. Phys., 21, 13067–13076, https://doi.org/10.5194/acp-21-13067-2021, https://doi.org/10.5194/acp-21-13067-2021, 2021
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Iodine is emitted from the ocean and helps to destroy ozone in the lower atmosphere before being taken up into aerosol particles. We measured the chemical forms of iodine in aerosols over the Atlantic Ocean, because some of these forms can return to the gas phase and destroy more ozone. Our results indicate that aerosol acidity exerts a strong control on iodine speciation and therefore on its recycling behaviour and impact on ozone concentrations.
Hong Ren, Wei Hu, Lianfang Wei, Siyao Yue, Jian Zhao, Linjie Li, Libin Wu, Wanyu Zhao, Lujie Ren, Mingjie Kang, Qiaorong Xie, Sihui Su, Xiaole Pan, Zifa Wang, Yele Sun, Kimitaka Kawamura, and Pingqing Fu
Atmos. Chem. Phys., 21, 12949–12963, https://doi.org/10.5194/acp-21-12949-2021, https://doi.org/10.5194/acp-21-12949-2021, 2021
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This study presents vertical profiles of biogenic and anthropogenic secondary organic aerosols (SOAs) in the urban boundary layer based on a 325 m tower in Beijing in late summer. The increases in the isoprene and toluene SOAs with height were found to be more related to regional transport, whereas the decrease in those from monoterpenes and sesquiterpene were more subject to local emissions. Such complicated vertical distributions of SOA should be considered in future modeling work.
Vaios Moschos, Martin Gysel-Beer, Robin L. Modini, Joel C. Corbin, Dario Massabò, Camilla Costa, Silvia G. Danelli, Athanasia Vlachou, Kaspar R. Daellenbach, Sönke Szidat, Paolo Prati, André S. H. Prévôt, Urs Baltensperger, and Imad El Haddad
Atmos. Chem. Phys., 21, 12809–12833, https://doi.org/10.5194/acp-21-12809-2021, https://doi.org/10.5194/acp-21-12809-2021, 2021
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This study provides a holistic approach to studying the spectrally resolved light absorption by atmospheric brown carbon (BrC) and black carbon using long time series of daily samples from filter-based measurements. The obtained results provide (1) a better understanding of the aerosol absorption profile and its dependence on BrC and on lensing from less absorbing coatings and (2) an estimation of the most important absorbers at typical European locations.
Michele Bertò, David Cappelletti, Elena Barbaro, Cristiano Varin, Jean-Charles Gallet, Krzysztof Markowicz, Anna Rozwadowska, Mauro Mazzola, Stefano Crocchianti, Luisa Poto, Paolo Laj, Carlo Barbante, and Andrea Spolaor
Atmos. Chem. Phys., 21, 12479–12493, https://doi.org/10.5194/acp-21-12479-2021, https://doi.org/10.5194/acp-21-12479-2021, 2021
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We present the daily and seasonal variability in black carbon (BC) in surface snow inferred from two specific experiments based on the hourly and daily time resolution sampling during the Arctic spring in Svalbard. These unique data sets give us, for the first time, the opportunity to evaluate the associations between the observed surface snow BC mass concentration and a set of predictors corresponding to the considered meteorological and snow physico-chemical parameters.
Zhuohui Lin, Yonghong Wang, Feixue Zheng, Ying Zhou, Yishuo Guo, Zemin Feng, Chang Li, Yusheng Zhang, Simo Hakala, Tommy Chan, Chao Yan, Kaspar R. Daellenbach, Biwu Chu, Lubna Dada, Juha Kangasluoma, Lei Yao, Xiaolong Fan, Wei Du, Jing Cai, Runlong Cai, Tom V. Kokkonen, Putian Zhou, Lili Wang, Tuukka Petäjä, Federico Bianchi, Veli-Matti Kerminen, Yongchun Liu, and Markku Kulmala
Atmos. Chem. Phys., 21, 12173–12187, https://doi.org/10.5194/acp-21-12173-2021, https://doi.org/10.5194/acp-21-12173-2021, 2021
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We find that ammonium nitrate and aerosol water content contributed most during low mixing layer height conditions; this may further trigger enhanced formation of sulfate and organic aerosol via heterogeneous reactions. The results of this study contribute towards a more detailed understanding of the aerosol–chemistry–radiation–boundary layer feedback that is likely to be responsible for explosive aerosol mass growth events in urban Beijing.
Zhenzhen Wang, Di Wu, Zhuoyu Li, Xiaona Shang, Qing Li, Xiang Li, Renjie Chen, Haidong Kan, Huiling Ouyang, Xu Tang, and Jianmin Chen
Atmos. Chem. Phys., 21, 12227–12241, https://doi.org/10.5194/acp-21-12227-2021, https://doi.org/10.5194/acp-21-12227-2021, 2021
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This study firstly investigates the composition of sugars in the fine fraction of aerosol over three sites in southwest China. The result suggested no significant reduction in biomass burning emissions in southwest Yunnan Province to some extent. The result shown sheds light on the contributions of biomass burning and the characteristics of biogenic saccharides in these regions, which could be further applied to regional source apportionment models and global climate models.
Chao Qin, Yafeng Gou, Yuhang Wang, Yuhao Mao, Hong Liao, Qin'geng Wang, and Mingjie Xie
Atmos. Chem. Phys., 21, 12141–12153, https://doi.org/10.5194/acp-21-12141-2021, https://doi.org/10.5194/acp-21-12141-2021, 2021
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In this study, we found that the aqueous solution in aerosols is an important absorbing phase for gaseous polyols in the atmosphere, indicating that the dissolution in aerosol liquid water should not be ignored when investigating gas–particle partitioning of water-soluble organics. The exponential increase in effective partitioning coefficients of polyol tracers with sulfate ion concentrations could be attributed to organic–inorganic interactions in the particle phase.
Nana Suto and Hiroto Kawashima
Atmos. Chem. Phys., 21, 11815–11828, https://doi.org/10.5194/acp-21-11815-2021, https://doi.org/10.5194/acp-21-11815-2021, 2021
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The sources and seasonal trends of water-soluble organic carbon (WSOC) in PM2.5 on long-term trends at two sites in Japan are investigated by carbon isotope ratio (δ13C) of WSOC. At the rural site, the δ13C of WSOC from autumn to spring was concluded to reflect mainly the biomass burning of rice straw. The heaviest δ13C of WSOC from February to April 2019 might reflect long-range transport of particles resulting from the overseas burning of C4 plants such as corn.
Luis M. F. Barreira, Arttu Ylisirniö, Iida Pullinen, Angela Buchholz, Zijun Li, Helina Lipp, Heikki Junninen, Urmas Hõrrak, Steffen M. Noe, Alisa Krasnova, Dmitrii Krasnov, Kaia Kask, Eero Talts, Ülo Niinemets, Jose Ruiz-Jimenez, and Siegfried Schobesberger
Atmos. Chem. Phys., 21, 11781–11800, https://doi.org/10.5194/acp-21-11781-2021, https://doi.org/10.5194/acp-21-11781-2021, 2021
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We present results from PM1 atmospheric composition and concentration measurements performed in a springtime hemiboreal forest. Sesquiterpene mixing ratios and particle-phase concentrations of corresponding oxidation products were rapidly increasing on some early mornings. The particle volatility suggested that condensable sesquiterpene oxidation products are rapidly formed in the atmosphere. The results revealed the importance of sesquiterpenes for secondary organic aerosol particulate mass.
Ernesto Reyes-Villegas, Upasana Panda, Eoghan Darbyshire, James M. Cash, Rutambhara Joshi, Ben Langford, Chiara F. Di Marco, Neil J. Mullinger, Mohammed S. Alam, Leigh R. Crilley, Daniel J. Rooney, W. Joe F. Acton, Will Drysdale, Eiko Nemitz, Michael Flynn, Aristeidis Voliotis, Gordon McFiggans, Hugh Coe, James Lee, C. Nicholas Hewitt, Mathew R. Heal, Sachin S. Gunthe, Tuhin K. Mandal, Bhola R. Gurjar, Shivani, Ranu Gadi, Siddhartha Singh, Vijay Soni, and James D. Allan
Atmos. Chem. Phys., 21, 11655–11667, https://doi.org/10.5194/acp-21-11655-2021, https://doi.org/10.5194/acp-21-11655-2021, 2021
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This paper shows the first multisite online measurements of PM1 in Delhi, India, with measurements over different seasons in Old Delhi and New Delhi in 2018. Organic aerosol (OA) source apportionment was performed using positive matrix factorisation (PMF). Traffic was the main primary aerosol source for both OAs and black carbon, seen with PMF and Aethalometer model analysis, indicating that control of primary traffic exhaust emissions would make a significant reduction to Delhi air pollution.
Qiaorong Xie, Sihui Su, Jing Chen, Yuqing Dai, Siyao Yue, Hang Su, Haijie Tong, Wanyu Zhao, Lujie Ren, Yisheng Xu, Dong Cao, Ying Li, Yele Sun, Zifa Wang, Cong-Qiang Liu, Kimitaka Kawamura, Guibin Jiang, Yafang Cheng, and Pingqing Fu
Atmos. Chem. Phys., 21, 11453–11465, https://doi.org/10.5194/acp-21-11453-2021, https://doi.org/10.5194/acp-21-11453-2021, 2021
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This study investigated the role of nighttime chemistry during Chinese New Year's Eve that enhances the formation of nitrooxy organosulfates in the aerosol phase. Results show that anthropogenic precursors, together with biogenic ones, considerably contribute to the formation of low-volatility nitrooxy OSs. Our study provides detailed molecular composition of firework-related aerosols, which gives new insights into the physicochemical properties and potential health effects of urban aerosols.
Congbo Song, Manuel Dall'Osto, Angelo Lupi, Mauro Mazzola, Rita Traversi, Silvia Becagli, Stefania Gilardoni, Stergios Vratolis, Karl Espen Yttri, David C. S. Beddows, Julia Schmale, James Brean, Agung Ghani Kramawijaya, Roy M. Harrison, and Zongbo Shi
Atmos. Chem. Phys., 21, 11317–11335, https://doi.org/10.5194/acp-21-11317-2021, https://doi.org/10.5194/acp-21-11317-2021, 2021
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We present a cluster analysis of relatively long-term (2015–2019) aerosol aerodynamic volume size distributions up to 20 μm in the Arctic for the first time. The study found that anthropogenic and natural aerosols comprised 27 % and 73 % of the occurrence of the coarse-mode aerosols, respectively. Our study shows that about two-thirds of the coarse-mode aerosols are related to two sea-spray-related aerosol clusters, indicating that sea spray aerosol may more complex in the Arctic environment.
Samuël Weber, Gaëlle Uzu, Olivier Favez, Lucille Joanna S. Borlaza, Aude Calas, Dalia Salameh, Florie Chevrier, Julie Allard, Jean-Luc Besombes, Alexandre Albinet, Sabrina Pontet, Boualem Mesbah, Grégory Gille, Shouwen Zhang, Cyril Pallares, Eva Leoz-Garziandia, and Jean-Luc Jaffrezo
Atmos. Chem. Phys., 21, 11353–11378, https://doi.org/10.5194/acp-21-11353-2021, https://doi.org/10.5194/acp-21-11353-2021, 2021
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Oxidative potential (OP) of aerosols is apportioned to the main PM sources found in 15 sites over France. The sources present clear distinct intrinsic OPs at a large geographic scale, and a drastic redistribution between the mass concentration and OP measured by both ascorbic acid and dithiothreitol is highlighted. Moreover, the high discrepancy between the mean and median contributions of the sources to the given metrics raises some important questions when dealing with health endpoints.
Jiao Tang, Jiaqi Wang, Guangcai Zhong, Hongxing Jiang, Yangzhi Mo, Bolong Zhang, Xiaofei Geng, Yingjun Chen, Jianhui Tang, Congguo Tian, Surat Bualert, Jun Li, and Gan Zhang
Atmos. Chem. Phys., 21, 11337–11352, https://doi.org/10.5194/acp-21-11337-2021, https://doi.org/10.5194/acp-21-11337-2021, 2021
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This article provides a combined EEM–PARAFAC and statistical analysis method to explore how excitation–emission matrix (EEM) chromophores influence BrC light absorption in soluble organic matter. The application enables us to deduce that BrC absorption is mainly dependent on longer-emission-wavelength chromophores largely associated with biomass burning emissions. This method promotes the application of EEM spectroscopy and helps us understand the light absorption of BrC in the atmosphere.
Benjamin A. Nault, Duseong S. Jo, Brian C. McDonald, Pedro Campuzano-Jost, Douglas A. Day, Weiwei Hu, Jason C. Schroder, James Allan, Donald R. Blake, Manjula R. Canagaratna, Hugh Coe, Matthew M. Coggon, Peter F. DeCarlo, Glenn S. Diskin, Rachel Dunmore, Frank Flocke, Alan Fried, Jessica B. Gilman, Georgios Gkatzelis, Jacqui F. Hamilton, Thomas F. Hanisco, Patrick L. Hayes, Daven K. Henze, Alma Hodzic, James Hopkins, Min Hu, L. Greggory Huey, B. Thomas Jobson, William C. Kuster, Alastair Lewis, Meng Li, Jin Liao, M. Omar Nawaz, Ilana B. Pollack, Jeffrey Peischl, Bernhard Rappenglück, Claire E. Reeves, Dirk Richter, James M. Roberts, Thomas B. Ryerson, Min Shao, Jacob M. Sommers, James Walega, Carsten Warneke, Petter Weibring, Glenn M. Wolfe, Dominique E. Young, Bin Yuan, Qiang Zhang, Joost A. de Gouw, and Jose L. Jimenez
Atmos. Chem. Phys., 21, 11201–11224, https://doi.org/10.5194/acp-21-11201-2021, https://doi.org/10.5194/acp-21-11201-2021, 2021
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Secondary organic aerosol (SOA) is an important aspect of poor air quality for urban regions around the world, where a large fraction of the population lives. However, there is still large uncertainty in predicting SOA in urban regions. Here, we used data from 11 urban campaigns and show that the variability in SOA production in these regions is predictable and is explained by key emissions. These results are used to estimate the premature mortality associated with SOA in urban regions.
Yuan Cheng, Qin-qin Yu, Jiu-meng Liu, Xu-bing Cao, Ying-jie Zhong, Zhen-yu Du, Lin-lin Liang, Guan-nan Geng, Wan-li Ma, Hong Qi, Qiang Zhang, and Ke-bin He
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2021-522, https://doi.org/10.5194/acp-2021-522, 2021
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Open burning policies in Heilongjiang Province experienced a rapid transition during 2018 to 2020. This study evaluated the responses of PM2.5 pollution to this transition, and suggested neither of the policies could be considered successful. In addition, heterogeneous reactions were found to be at play in secondary aerosol formation, even in the frigid atmosphere in Heilongjiang. The unique haze in Northeast China deserves more attention.
Evelyn Freney, Karine Sellegri, Alessia Nicosia, Leah R. Williams, Matteo Rinaldi, Jonathan T. Trueblood, André S. H. Prévôt, Melilotus Thyssen, Gérald Grégori, Nils Haëntjens, Julie Dinasquet, Ingrid Obernosterer, France Van Wambeke, Anja Engel, Birthe Zäncker, Karine Desboeufs, Eija Asmi, Hilkka Timonen, and Cécile Guieu
Atmos. Chem. Phys., 21, 10625–10641, https://doi.org/10.5194/acp-21-10625-2021, https://doi.org/10.5194/acp-21-10625-2021, 2021
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In this work, we present observations of the organic aerosol content in primary sea spray aerosols (SSAs) continuously generated along a 5-week cruise in the Mediterranean. This information is combined with seawater biogeochemical properties also measured continuously along the ship track to develop a number of parametrizations that can be used in models to determine SSA organic content in oligotrophic waters that represent 60 % of the oceans from commonly measured seawater variables.
James M. Cash, Ben Langford, Chiara Di Marco, Neil J. Mullinger, James Allan, Ernesto Reyes-Villegas, Ruthambara Joshi, Mathew R. Heal, W. Joe F. Acton, C. Nicholas Hewitt, Pawel K. Misztal, Will Drysdale, Tuhin K. Mandal, Shivani, Ranu Gadi, Bhola Ram Gurjar, and Eiko Nemitz
Atmos. Chem. Phys., 21, 10133–10158, https://doi.org/10.5194/acp-21-10133-2021, https://doi.org/10.5194/acp-21-10133-2021, 2021
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We present the first real-time composition of submicron particulate matter (PM1) in Old Delhi using high-resolution aerosol mass spectrometry. Seasonal analysis shows peak concentrations occur during the post-monsoon, and novel-tracers reveal the largest sources are a combination of local open and regional crop residue burning. Strong links between increased chloride aerosol concentrations and burning sources of PM1 suggest burning sources are responsible for the post-monsoon chloride peak.
Liine Heikkinen, Mikko Äijälä, Kaspar R. Daellenbach, Gang Chen, Olga Garmash, Diego Aliaga, Frans Graeffe, Meri Räty, Krista Luoma, Pasi Aalto, Markku Kulmala, Tuukka Petäjä, Douglas Worsnop, and Mikael Ehn
Atmos. Chem. Phys., 21, 10081–10109, https://doi.org/10.5194/acp-21-10081-2021, https://doi.org/10.5194/acp-21-10081-2021, 2021
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In many locations worldwide aerosol particles have been shown to be made up of organic aerosol (OA). The boreal forest is a region where aerosol particles possess a high OA mass fraction. Here, we studied OA composition using the longest time series of OA composition ever obtained from a boreal environment. For this purpose, we tested a new analysis framework and discovered that most of the OA was highly oxidized, with strong seasonal behaviour reflecting different sources in summer and winter.
Yandong Tong, Veronika Pospisilova, Lu Qi, Jing Duan, Yifang Gu, Varun Kumar, Pragati Rai, Giulia Stefenelli, Liwei Wang, Ying Wang, Haobin Zhong, Urs Baltensperger, Junji Cao, Ru-Jin Huang, André S. H. Prévôt, and Jay G. Slowik
Atmos. Chem. Phys., 21, 9859–9886, https://doi.org/10.5194/acp-21-9859-2021, https://doi.org/10.5194/acp-21-9859-2021, 2021
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We investigate SOA sources and formation processes by a field deployment of the EESI-TOF-MS and L-TOF AMS in Beijing in late autumn and early winter. Our study shows that the sources and processes giving rise to haze events in Beijing are variable and seasonally dependent: (1) in the heating season, SOA formation is driven by oxidation of aromatics from solid fuel combustion; and (2) under high-NOx and RH conditions, aqueous-phase chemistry can be a major contributor to SOA formation.
Sehyun Jang, Ki-Tae Park, Kitack Lee, Young Jun Yoon, Kitae Kim, Hyun Young Chung, Eunho Jang, Silvia Becagli, Bang Yong Lee, Rita Traversi, Konstantinos Eleftheriadis, Radovan Krejci, and Ove Hermansen
Atmos. Chem. Phys., 21, 9761–9777, https://doi.org/10.5194/acp-21-9761-2021, https://doi.org/10.5194/acp-21-9761-2021, 2021
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This study provides comprehensive datasets encompassing seasonal and interannual variations in sulfate and MSA concentration in aerosol particles in the Arctic atmosphere. As oxidation products of DMS have important roles in new particle formation and growth, we focused on factors affecting their variability and the branching ratio of DMS oxidation. We found a strong correlation between the ratio and the light condition, chemical properties of particles, and biological activities near Svalbard.
Lucille Joanna S. Borlaza, Samuël Weber, Jean-Luc Jaffrezo, Stephan Houdier, Rémy Slama, Camille Rieux, Alexandre Albinet, Steve Micallef, Cécile Trébluchon, and Gaëlle Uzu
Atmos. Chem. Phys., 21, 9719–9739, https://doi.org/10.5194/acp-21-9719-2021, https://doi.org/10.5194/acp-21-9719-2021, 2021
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With an enhanced source apportionment obtained in a companion paper, this paper acquires more understanding of the spatiotemporal associations of the sources of PM to oxidative potential (OP), an emerging health-based metric. Multilayer perceptron neural network analysis was used to apportion OP from PM sources. Results showed that such a methodology is as robust as the linear classical inversion and permits an improvement in the OP prediction when local features or non-linear effects occur.
Baozhu Ge, Danhui Xu, Oliver Wild, Xuefeng Yao, Junhua Wang, Xueshun Chen, Qixin Tan, Xiaole Pan, and Zifa Wang
Atmos. Chem. Phys., 21, 9441–9454, https://doi.org/10.5194/acp-21-9441-2021, https://doi.org/10.5194/acp-21-9441-2021, 2021
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In this study, an improved sequential sampling method is developed and implemented to estimate the contribution of below-cloud and in-cloud wet deposition over four years of measurements in Beijing. We find that the contribution of below-cloud scavenging for Ca2+, SO4 2–, and NH4+ decreases from above 50 % in 2014 to below 40 % in 2017. This suggests that the Action Plan has mitigated particulate matter pollution in the surface layer and hence decreased scavenging due to the washout process.
Kai Wang, Ru-Jin Huang, Martin Brüggemann, Yun Zhang, Lu Yang, Haiyan Ni, Jie Guo, Meng Wang, Jiajun Han, Merete Bilde, Marianne Glasius, and Thorsten Hoffmann
Atmos. Chem. Phys., 21, 9089–9104, https://doi.org/10.5194/acp-21-9089-2021, https://doi.org/10.5194/acp-21-9089-2021, 2021
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Here we present the detailed molecular composition of the organic aerosol collected in three eastern Chinese cities from north to south, Changchun, Shanghai and Guangzhou, by applying LC–Orbitrap analysis. Accordingly, the aromaticity degree of chemical compounds decreases from north to south, while the oxidation degree increases from north to south, which can be explained by the different anthropogenic emissions and photochemical oxidation processes.
Charlotte M. Beall, Jennifer M. Michaud, Meredith A. Fish, Julie Dinasquet, Gavin C. Cornwell, M. Dale Stokes, Michael D. Burkart, Thomas C. Hill, Paul J. DeMott, and Kimberly A. Prather
Atmos. Chem. Phys., 21, 9031–9045, https://doi.org/10.5194/acp-21-9031-2021, https://doi.org/10.5194/acp-21-9031-2021, 2021
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Ice-nucleating particles (INPs) can influence multiple climate-relevant cloud properties by triggering droplet freezing at relative humidities below or temperatures above the freezing point of water. The ocean is a significant INP source; however, the specific identities of marine INPs remain largely unknown. Here, we identify 14 ice-nucleating microbes from aerosol and precipitation samples collected at a coastal site in southern California, two or more of which are likely marine.
Jose Ruiz-Jimenez, Magdalena Okuljar, Outi-Maaria Sietiö, Giorgia Demaria, Thanaporn Liangsupree, Elisa Zagatti, Juho Aalto, Kari Hartonen, Jussi Heinonsalo, Jaana Bäck, Tuukka Petäjä, and Marja-Liisa Riekkola
Atmos. Chem. Phys., 21, 8775–8790, https://doi.org/10.5194/acp-21-8775-2021, https://doi.org/10.5194/acp-21-8775-2021, 2021
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Altogether, 84 size-segregated aerosol samples from four particle size fractions were collected at the Station for Measuring Forest Ecosystem-Atmosphere Relations, Hyytiälä, Finland, in autumn 2017 for the clarification of the complex interrelationships between airborne and particulate chemical traces, amino acids and saccharides, gene copy numbers (16S and 18S for bacteria and fungi, respectively), gas-phase chemistry, and the particle size distribution.
Djacinto Monteiro dos Santos, Luciana Varanda Rizzo, Samara Carbone, Patrick Schlag, and Paulo Artaxo
Atmos. Chem. Phys., 21, 8761–8773, https://doi.org/10.5194/acp-21-8761-2021, https://doi.org/10.5194/acp-21-8761-2021, 2021
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The metropolitan area of São Paulo (MASP), with very extensive biofuel use, has unique atmospheric chemistry among world megacities. In this study, we examine the complex relationships between aerosol chemical composition and particle size distribution. Our findings provide a better understanding of the dynamics of the physicochemical properties of submicron particles and highlight the key role of secondary organic aerosol formation in the pollution levels in São Paulo.
Rui Li, Yilong Zhao, Hongbo Fu, Jianmin Chen, Meng Peng, and Chunying Wang
Atmos. Chem. Phys., 21, 8677–8692, https://doi.org/10.5194/acp-21-8677-2021, https://doi.org/10.5194/acp-21-8677-2021, 2021
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Based on a random forest model, the strict lockdown measures significantly decreased primary components such as Cr (−67 %) and Fe (−61 %) in PM2.5 (p < 0.01), whereas the higher relative humidity (RH) and NH3 level and the lower air temperature (T) remarkably enhanced the production of secondary aerosol including SO42− (29 %), NO3− (29 %), and NH4+ (21 %) (p < 0.05). The natural experiment suggested that the NH3 emission should be strictly controlled.
Xinyao Feng, Yingze Tian, Qianqian Xue, Danlin Song, Fengxia Huang, and Yinchang Feng
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2021-311, https://doi.org/10.5194/acp-2021-311, 2021
Revised manuscript accepted for ACP
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This study focused on PM2.5 compositions and sources, and explored their spatiotemporal and policy-related variations based on observation at 19 sites during wintertime of 2015–2019 in a fast-developing megacity. We found that PM2.5 compositions for outer-most zone in 2019 were similar to that for core zone two or three years ago. Percentage contributions of coal and biomass combustion dramatically declined in core zone, while traffic source showed an increasing trend.
Yue Zhou, Christopher P. West, Anusha P. S. Hettiyadura, Xiaoying Niu, Hui Wen, Jiecan Cui, Tenglong Shi, Wei Pu, Xin Wang, and Alexander Laskin
Atmos. Chem. Phys., 21, 8531–8555, https://doi.org/10.5194/acp-21-8531-2021, https://doi.org/10.5194/acp-21-8531-2021, 2021
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We present a comprehensive characterization of water-soluble organic carbon (WSOC) in seasonal snow of northwestern China. We applied complementary multimodal analytical techniques to investigate bulk and molecular-level composition, optical properties, and sources of WSOC. For the first time, we estimated the extent of radiative forcing due to WSOC in snow using a model simulation and showed the profound influences of WSOC on the energy budget of midlatitude seasonal snowpack.
Quan Liu, Dantong Liu, Yangzhou Wu, Kai Bi, Wenkang Gao, Ping Tian, Delong Zhao, Siyuan Li, Chenjie Yu, Yunfei Wu, Kang Hu, Shuo Ding, Qian Gao, Fei Wang, Hui He, Mengyu Huang, and Deping Ding
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2021-362, https://doi.org/10.5194/acp-2021-362, 2021
Revised manuscript accepted for ACP
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Through simultaneous online measurements of detailed aerosol compositions at both surface and surface-influenced mountain sites, the evolution of aerosol composition during daytime vertical transport was investigated. The results show that from surface to the top of the PBL, the oxidation state of organic aerosol had been significantly enhanced due to evaporation and further oxidation on these evaporated gases.
Bingqing Zhang, Huizhong Shen, Pengfei Liu, Hongyu Guo, Yongtao Hu, Yilin Chen, Shaodong Xie, Ziyan Xi, T. Nash Skipper, and Armistead G. Russell
Atmos. Chem. Phys., 21, 8341–8356, https://doi.org/10.5194/acp-21-8341-2021, https://doi.org/10.5194/acp-21-8341-2021, 2021
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Extended ground-level measurements are coupled with model simulations to comprehensively compare the aerosol acidity in China and the United States. Aerosols in China are significantly less acidic than those in the United States, with pH values 1–2 units higher. Higher aerosol mass concentrations and the abundance of ammonia and ammonium in China, compared to the United States, are leading causes of the pH difference between these two countries.
Marta Via, María Cruz Minguillón, Cristina Reche, Xavier Querol, and Andrés Alastuey
Atmos. Chem. Phys., 21, 8323–8339, https://doi.org/10.5194/acp-21-8323-2021, https://doi.org/10.5194/acp-21-8323-2021, 2021
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Atmospheric pollutants have been measured in an urban environment by means of state-of-the-art techniques, allowing the origin and the sources of pollution to be identified. Recent years are shown to be increasingly dominated by non-directly emitted particulate matter. Knowledge about the sources of atmospheric pollutants is necessary to design effective mitigation policies.
Dac-Loc Nguyen, Hendryk Czech, Simone M. Pieber, Jürgen Schnelle-Kreis, Martin Steinbacher, Jürgen Orasche, Stephan Henne, Olga B. Popovicheva, Gülcin Abbaszade, Guenter Engling, Nicolas Bukowiecki, Nhat-Anh Nguyen, Xuan-Anh Nguyen, and Ralf Zimmermann
Atmos. Chem. Phys., 21, 8293–8312, https://doi.org/10.5194/acp-21-8293-2021, https://doi.org/10.5194/acp-21-8293-2021, 2021
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Southeast Asia is well-known for emission-intense and recurring wildfires and after-harvest crop residue burning during the pre-monsoon season from February to April. We describe a biomass burning (BB) plume arriving at remote Pha Din meteorological station, outline its carbonaceous particulate matter (PM) constituents based on more than 50 target compounds and discuss possible BB sources. This study adds valuable information on chemical PM composition for a region with scarce data availability.
Amy Hrdina, Jennifer G. Murphy, Anna Gannet Hallar, John C. Lin, Alexander Moravek, Ryan Bares, Ross C. Petersen, Alessandro Franchin, Ann M. Middlebrook, Lexie Goldberger, Ben H. Lee, Munkh Baasandorj, and Steven S. Brown
Atmos. Chem. Phys., 21, 8111–8126, https://doi.org/10.5194/acp-21-8111-2021, https://doi.org/10.5194/acp-21-8111-2021, 2021
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Wintertime air pollution in the Salt Lake Valley is primarily composed of ammonium nitrate, which is formed when gas-phase ammonia and nitric acid react. The major point in this work is that the chemical composition of snow tells a very different story to what we measured in the atmosphere. With the dust–sea salt cations observed in PM2.5 and particle sizing data, we can estimate how much nitric acid may be lost to dust–sea salt that is not accounted for and how much more PM2.5 this could form.
Vincent Michoud, Elise Hallemans, Laura Chiappini, Eva Leoz-Garziandia, Aurélie Colomb, Sébastien Dusanter, Isabelle Fronval, François Gheusi, Jean-Luc Jaffrezo, Thierry Léonardis, Nadine Locoge, Nicolas Marchand, Stéphane Sauvage, Jean Sciare, and Jean-François Doussin
Atmos. Chem. Phys., 21, 8067–8088, https://doi.org/10.5194/acp-21-8067-2021, https://doi.org/10.5194/acp-21-8067-2021, 2021
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A multiphasic molecular characterization of oxygenated compounds has been carried out during the ChArMEx field campaign using offline analysis. It leads to the identification of 97 different compounds in the gas and aerosol phases and reveals the important contribution of organic acids to organic aerosol. In addition, comparison between experimental and theoretical partitioning coefficients revealed in most cases a large underestimation by the theory reaching 1 to 7 orders of magnitude.
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
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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.
Jean-Philippe Putaud, Luca Pozzoli, Enrico Pisoni, Sebastiao Martins Dos Santos, Friedrich Lagler, Guido Lanzani, Umberto Dal Santo, and Augustin Colette
Atmos. Chem. Phys., 21, 7597–7609, https://doi.org/10.5194/acp-21-7597-2021, https://doi.org/10.5194/acp-21-7597-2021, 2021
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To determine the impact of the COVID lockdown on air quality in northern Italy, measurements of atmospheric pollutants (NO2, PM10, O3, NO, SO2 ) were compared to the output of a model ignoring the lockdown. We found that NO2 decreased on average by −30 % to −40 %. Unlike NO2, PM10 was not significantly affected due to the compensation of decreased emissions from traffic by increased emissions from domestic heating and/or by changes in atmospheric chemistry enhancing secondary aerosol formation.
Benjamin Chazeau, Brice Temime-Roussel, Grégory Gille, Boualem Mesbah, Barbara D'Anna, Henri Wortham, and Nicolas Marchand
Atmos. Chem. Phys., 21, 7293–7319, https://doi.org/10.5194/acp-21-7293-2021, https://doi.org/10.5194/acp-21-7293-2021, 2021
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The temporal trends in the chemical composition and particle number of the submicron aerosols in a Mediterranean city, Marseille, are investigated over 14 months. Fifteen days were found to exceed the WHO PM2.5 daily limit (25 µg m−3) only during the cold period, with two distinct origins: local pollution events with an increased fraction of the carbonaceous fraction due to domestic wood burning and long-range pollution events with a high level of oxygenated organic aerosol and ammonium nitrate.
Karl Espen Yttri, Francesco Canonaco, Sabine Eckhardt, Nikolaos Evangeliou, Markus Fiebig, Hans Gundersen, Anne-Gunn Hjellbrekke, Cathrine Lund Myhre, Stephen Matthew Platt, André S. H. Prévôt, David Simpson, Sverre Solberg, Jason Surratt, Kjetil Tørseth, Hilde Uggerud, Marit Vadset, Xin Wan, and Wenche Aas
Atmos. Chem. Phys., 21, 7149–7170, https://doi.org/10.5194/acp-21-7149-2021, https://doi.org/10.5194/acp-21-7149-2021, 2021
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Carbonaceous aerosol sources and trends were studied at the Birkenes Observatory. A large decrease in elemental carbon (EC; 2001–2018) and a smaller decline in levoglucosan (2008–2018) suggest that organic carbon (OC)/EC from traffic/industry is decreasing, whereas the abatement of OC/EC from biomass burning has been less successful. Positive matrix factorization apportioned 72 % of EC to fossil fuel sources and 53 % (PM2.5) and 78 % (PM10–2.5) of OC to biogenic sources.
Xiaojing Shen, Junying Sun, Fangqun Yu, Ying Wang, Junting Zhong, Yangmei Zhang, Xinyao Hu, Can Xia, Sinan Zhang, and Xiaoye Zhang
Atmos. Chem. Phys., 21, 7039–7052, https://doi.org/10.5194/acp-21-7039-2021, https://doi.org/10.5194/acp-21-7039-2021, 2021
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In this work, we revealed the changes of PNSD and NPF events during the COVID-19 lockdown period in Beijing, China, to illustrate the impact of reduced primary emission and elavated atmospheric oxidized capicity on the nucleation and growth processes. The subsequent growth of nucleated particles and their contribution to the aerosol pollution formation were also explored, to highlight the necessity of controlling the nanoparticles in the future air quality management.
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
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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.
Sanna Saarikoski, Jarkko V. Niemi, Minna Aurela, Liisa Pirjola, Anu Kousa, Topi Rönkkö, and Hilkka Timonen
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2021-231, https://doi.org/10.5194/acp-2021-231, 2021
Revised manuscript accepted for ACP
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This study presents the main sources of black carbon (BC) at two urban environments. The largest fraction of BC originated from biomass burning at the residential site (38 %) and from vehicular emissions (57 %) at the street canyon. Also, a significant fraction of BC was associated with urban background or long-range transport. The data are needed by modelers and authorities when assessing climate and air quality impact of BC as well as directing the emission legislation and mitigation actions.
Luis M. F. Barreira, Aku Helin, Minna Aurela, Kimmo Teinilä, Milla Friman, Leena Kangas, Jarkko V. Niemi, Harri Portin, Anu Kousa, Liisa Pirjola, Topi Rönkkö, Sanna Saarikoski, and Hilkka Timonen
Atmos. Chem. Phys., 21, 6297–6314, https://doi.org/10.5194/acp-21-6297-2021, https://doi.org/10.5194/acp-21-6297-2021, 2021
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We present results from the long-term measurements (5 years) of highly time-resolved atmospheric PM1 composition at an urban street canyon site. Overall, the results increased knowledge of the variability of PM1 concentration, composition, and sources in a traffic site and the implications for urban air quality. The investigation of pollution episodes showed that both local and long-range-transported pollutants can still cause elevated PM1 and PM2.5 concentrations in northern Europe.
John MacInnis, Jai Prakash Chaubey, Crystal Weagle, David Atkinson, and Rachel Ying-Wen Chang
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2021-262, https://doi.org/10.5194/acp-2021-262, 2021
Revised manuscript accepted for ACP
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This study measured particulate matter in the western Canadian Arctic during 2018 as part of the Year of Polar Prediction. It was found that the particles were likely from the ocean, soil, road dust, and combustion. The concentrations of small aerosol particles, which can affect human health, were low, suggesting they had little impact on local air quality. These results can be used to understand future changes in local aerosol particle sources and concentrations.
Genevieve Rose Lorenzo, Paola Angela Bañaga, Maria Obiminda Cambaliza, Melliza Templonuevo Cruz, Mojtaba AzadiAghdam, Avelino Arellano, Grace Betito, Rachel Braun, Andrea F. Corral, Hossein Dadashazar, Eva-Lou Edwards, Edwin Eloranta, Robert Holz, Gabrielle Leung, Lin Ma, Alexander B. MacDonald, Jeffrey S. Reid, James Bernard Simpas, Connor Stahl, Shane Marie Visaga, and Armin Sorooshian
Atmos. Chem. Phys., 21, 6155–6173, https://doi.org/10.5194/acp-21-6155-2021, https://doi.org/10.5194/acp-21-6155-2021, 2021
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Firework emissions change the physicochemical and optical properties of water-soluble particles, which subsequently alters the background aerosol’s respirability, influence on surroundings, ability to uptake gases, and viability as cloud condensation nuclei (CCN). There was heavy aerosol loading due to fireworks in the boundary layer. The aerosol constituents were largely water-soluble and submicrometer in size due to both inorganic salts in firework materials and gas-to-particle conversion.
Magdalena Reizer, Giulia Calzolai, Katarzyna Maciejewska, José A. G. Orza, Luca Carraresi, Franco Lucarelli, and Katarzyna Juda-Rezler
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2021-253, https://doi.org/10.5194/acp-2021-253, 2021
Revised manuscript accepted for ACP
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Elemental composition of atmospheric PM2.5 and PM2.5-10 was measured during wintertime with 1-hour resolution by the use of “streaker” sampler for the first time at Central European urban background site. A set of multivariate, wind- and trajectory-based receptor models identified main sources of ambient aerosol. Fine PM fraction was mainly comprised of regionally transported aged secondary sulfate from solid fuel combustion in residential sector, while coarse mode showed traffic-related origin.
Yutong Liang, Coty N. Jen, Robert J. Weber, Pawel K. Misztal, and Allen H. Goldstein
Atmos. Chem. Phys., 21, 5719–5737, https://doi.org/10.5194/acp-21-5719-2021, https://doi.org/10.5194/acp-21-5719-2021, 2021
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This article reports the molecular composition of smoke particles people in SF Bay Area were exposed to during northern California wildfires in Oct. 2017. Major components are sugars, acids, aromatics, and terpenoids. These observations can be used to better understand health impacts of smoke exposure. Tracer compounds indicate which fuels burned, including diterpenoids for softwood and syringyls for hardwood. A statistical analysis reveals a group of secondary compounds formed in daytime aging.
Steven J. Campbell, Kate Wolfer, Battist Utinger, Joe Westwood, Zhi-Hui Zhang, Nicolas Bukowiecki, Sarah S. Steimer, Tuan V. Vu, Jingsha Xu, Nicholas Straw, Steven Thomson, Atallah Elzein, Yele Sun, Di Liu, Linjie Li, Pingqing Fu, Alastair C. Lewis, Roy M. Harrison, William J. Bloss, Miranda Loh, Mark R. Miller, Zongbo Shi, and Markus Kalberer
Atmos. Chem. Phys., 21, 5549–5573, https://doi.org/10.5194/acp-21-5549-2021, https://doi.org/10.5194/acp-21-5549-2021, 2021
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In this study, we quantify PM2.5 oxidative potential (OP), a metric widely suggested as a potential measure of particle toxicity, in Beijing in summer and winter using four acellular assays. We correlate PM2.5 OP with a comprehensive range of atmospheric and particle composition measurements, demonstrating inter-assay differences and seasonal variation of PM2.5 OP. Using multivariate statistical analysis, we highlight specific particle chemical components and sources that influence OP.
Cited articles
Adams, P. J., Seinfeld, J. H., and Koch, D. M.: Global concentrations of
tropospheric sulfate, nitrate, and ammonium aerosol simulated in a general
circulation model, J. Geophys. Res.-Atmos., 104, 13791–13823,
https://doi.org/10.1029/1999JD900083, 1999. a
Ansari, A. S. and Pandis, S. N.: Response of inorganic PM to precursor
concentrations, Environ. Sci. Technol., 32, 2706–2714,
https://doi.org/10.1021/es971130j, 1998. a
Artíñano, B., Pujadas, M., Alonso-Blanco, E., Becerril-Valle, M., Coz,
E., Gómez-Moreno, F. J., Salvador, P., Nuñez, L., Palacios, M., and
Diaz, E.: Real-time monitoring of atmospheric ammonia during a pollution
episode in Madrid (Spain), Atmos. Environ., 189, 80–88,
https://doi.org/10.1016/j.atmosenv.2018.06.037, 2018. a, b
Athanasopoulou, E., Tombrou, M., Pandis, S. N., and Russell, A. G.: The role of sea-salt emissions and heterogeneous chemistry in the air quality of polluted coastal areas, Atmos. Chem. Phys., 8, 5755–5769, https://doi.org/10.5194/acp-8-5755-2008, 2008. a
Backes, A. M., Aulinger, A., Bieser, J., Matthias, V., and Quante, M.: Ammonia
emissions in Europe, part II: How ammonia emission abatement strategies
affect secondary aerosols, Atmos. Environ., 126, 153–161,
https://doi.org/10.1016/j.atmosenv.2015.11.039, 2016. a
Battaglia Jr., M. A., Douglas, S., and Hennigan, C. J.: Effect of the urban
heat island on aerosol pH, Environ. Sci. Technol., 51, 13095–13103,
https://doi.org/10.1021/acs.est.7b02786, 2017. a
Battaglia, M. A., Balasus, N., Ball, K., Caicedo, V., Delgado, R., Carlton, A. G., and Hennigan, C. J.: Urban aerosol chemistry at a land-water transition site during summer – Part 2: Aerosol pH and liquid water content, Atmos. Chem. Phys. Discuss. [preprint], https://doi.org/10.5194/acp-2021-368, in review, 2021. a, b, c, d
Bergström, A.-K. and Jansson, M.: Atmospheric nitrogen deposition has caused
nitrogen enrichment and eutrophication of lakes in the northern hemisphere,
Glob. Change Biol., 12, 635–643, https://doi.org/10.1111/j.1365-2486.2006.01129.x,
2006. a
Beyersdorf, A. J., Ziemba, L. D., Chen, G., Corr, C. A., Crawford, J. H., Diskin, G. S., Moore, R. H., Thornhill, K. L., Winstead, E. L., and Anderson, B. E.: The impacts of aerosol loading, composition, and water uptake on aerosol extinction variability in the Baltimore–Washington, D.C. region, Atmos. Chem. Phys., 16, 1003–1015, https://doi.org/10.5194/acp-16-1003-2016, 2016. a, b
Bian, H., Chin, M., Hauglustaine, D. A., Schulz, M., Myhre, G., Bauer, S. E., Lund, M. T., Karydis, V. A., Kucsera, T. L., Pan, X., Pozzer, A., Skeie, R. B., Steenrod, S. D., Sudo, K., Tsigaridis, K., Tsimpidi, A. P., and Tsyro, S. G.: Investigation of global particulate nitrate from the AeroCom phase III experiment, Atmos. Chem. Phys., 17, 12911–12940, https://doi.org/10.5194/acp-17-12911-2017, 2017. a
Bishop, G. A. and Stedman, D. H.: Reactive nitrogen species emission trends in
three light-/medium-duty United States fleets, Environ. Sci. Technol., 49,
11234–11240, https://doi.org/10.1021/acs.est.5b02392, 2015. a
Bouwman, A., Lee, D., Asman, W., Dentener, F., Van Der Hoek, K., and Olivier,
J.: A global high-resolution emission inventory for ammonia, Global
Biogeochem. Cy., 11, 561–587, https://doi.org/10.1029/97GB02266, 1997. a
Caicedo, V., Rappenglueck, B., Cuchiara, G., Flynn, J., Ferrare, R., Scarino,
A., Berkoff, T., Senff, C., Langford, A., and Lefer, B.: Bay breeze and sea
breeze circulation impacts on the planetary boundary layer and air quality
from an observed and modeled DISCOVER-AQ Texas case study, J. Geophys. Res.-Atmos., 124, 7359–7378, https://doi.org/10.1029/2019JD030523, 2019. a, b
Dammers, E., McLinden, C. A., Griffin, D., Shephard, M. W., Van Der Graaf, S., Lutsch, E., Schaap, M., Gainairu-Matz, Y., Fioletov, V., Van Damme, M., Whitburn, S., Clarisse, L., Cady-Pereira, K., Clerbaux, C., Coheur, P. F., and Erisman, J. W.: NH3 emissions from large point sources derived from CrIS and IASI satellite observations, Atmos. Chem. Phys., 19, 12261–12293, https://doi.org/10.5194/acp-19-12261-2019, 2019. a
de Gouw, J. A., Middlebrook, A. M., Warneke, C., Goldan, P. D., Kuster, W. C.,
Roberts, J. M., Fehsenfeld, F. C., Worsnop, D. R., Canagaratna, M. R.,
Pszenny, A. A. P., Keene, W. C., Marchewka, M., Bertman, S. B., and Bates,
T. S.: Budget of organic carbon in a polluted atmosphere: Results from the
New England Air Quality Study in 2002, J. Geophys. Res.-Atmos., 110, D16305,
https://doi.org/10.1029/2004JD005623, 2005. a
Ellis, R. A., Murphy, J. G., Pattey, E., van Haarlem, R., O'Brien, J. M., and Herndon, S. C.: Characterizing a Quantum Cascade Tunable Infrared Laser Differential Absorption Spectrometer (QC-TILDAS) for measurements of atmospheric ammonia, Atmos. Meas. Tech., 3, 397–406, https://doi.org/10.5194/amt-3-397-2010, 2010. a
Erisman, J. W., Otjes, R., Hensen, A., Jongejan, P., van den Bulk, P.,
Khlystov, A., Möls, H., and Slanina, S.: Instrument development and
application in studies and monitoring of ambient ammonia, Atmos. Environ.,
35, 1913–1922, https://doi.org/10.1016/S1352-2310(00)00544-6, 2001. a
Guo, H., Nenes, A., and Weber, R. J.: The underappreciated role of nonvolatile cations in aerosol ammonium-sulfate molar ratios, Atmos. Chem. Phys., 18, 17307–17323, https://doi.org/10.5194/acp-18-17307-2018, 2018. a
Hand, J. L., Schichtel, B. A., Malm, W. C., and Pitchford, M. L.: Particulate sulfate ion concentration and SO2 emission trends in the United States from the early 1990s through 2010, Atmos. Chem. Phys., 12, 10353–10365, https://doi.org/10.5194/acp-12-10353-2012, 2012a. a, b
Hand, J., Schichtel, B., Pitchford, M., Malm, W., and Frank, N.: Seasonal
composition of remote and urban fine particulate matter in the United States,
J. Geophys. Res.-Atmos., 117, D05209, https://doi.org/10.1029/2011JD017122, 2012b. a
Hauglustaine, D. A., Balkanski, Y., and Schulz, M.: A global model simulation of present and future nitrate aerosols and their direct radiative forcing of climate, Atmos. Chem. Phys., 14, 11031–11063, https://doi.org/10.5194/acp-14-11031-2014, 2014. a
Kean, A., Littlejohn, D., Ban-Weiss, G., Harley, R., Kirchstetter, T., and
Lunden, M.: Trends in on-road vehicle emissions of ammonia, Atmos. Environ.,
43, 1565–1570, https://doi.org/10.1016/j.atmosenv.2008.09.085, 2009. a, b
Keene, W. C., Moody, J. L., Galloway, J. N., Prospero, J. M., Cooper, O. R., Eckhardt, S., and Maben, J. R.: Long-term trends in aerosol and precipitation composition over the western North Atlantic Ocean at Bermuda, Atmos. Chem. Phys., 14, 8119–8135, https://doi.org/10.5194/acp-14-8119-2014, 2014. a
Larsen, R. K., Steinbacher, J. C., and Baker, J. E.: Ammonia Exchange between
the Atmosphere and the Surface Waters at Two Locations in the Chesapeake Bay,
Environ. Sci. Technol., 35, 4731–4738, https://doi.org/10.1021/es010755l, 2001. a, b, c
Li, M., Su, H., Li, G., Ma, N., Pöschl, U., and Cheng, Y.: Relative importance of gas uptake on aerosol and ground surfaces characterized by equivalent uptake coefficients, Atmos. Chem. Phys., 19, 10981–11011, https://doi.org/10.5194/acp-19-10981-2019, 2019. a
Loughner, C. P., Allen, D. J., Pickering, K. E., Zhang, D.-L., Shou, Y.-X., and
Dickerson, R. R.: Impact of fair-weather cumulus clouds and the Chesapeake
Bay breeze on pollutant transport and transformation, Atmos. Environ., 45,
4060–4072, https://doi.org/10.1016/j.atmosenv.2011.04.003, 2011. a
Loughner, C. P., Tzortziou, M., Follette-Cook, M., Pickering, K. E., Goldberg,
D., Satam, C., Weinheimer, A., Crawford, J. H., Knapp, D. J., Montzka, D. D.,
Diskin, G. S., and Dickerson, R. R.: Impact of bay-breeze circulations on
surface air quality and boundary layer export, J. Appl. Meteorol. Clim.,
53, 1697–1713, https://doi.org/10.1175/JAMC-D-13-0323.1, 2014. a
Loughner, C. P., Tzortziou, M., Shroder, S., and Pickering, K. E.: Enhanced dry
deposition of nitrogen pollution near coastlines: A case study covering the
Chesapeake Bay estuary and Atlantic Ocean coastline, J. Geophys. Res.-Atmos.,
121, 14221–14238, https://doi.org/10.1002/2016JD025571, 2016. a
MDE: Baltimore City Composting Facility, General facility information:
Emissions certification report, Maryland Department of the Environment Air
and Radiation Management Administration, 2019a. a
MDE: Grace Davison, General facility information: Emissions certification
report, Maryland Department of the Environment Air and Radiation Management
Administration, 2019b. a
Meng, W., Zhong, Q., Yun, X., Zhu, X., Huang, T., Shen, H., Chen, Y., Chen, H.,
Zhou, F., Liu, J., Wang, X., Zeng, E. Y., and Tao, S.: Improvement of a
Global High-Resolution Ammonia Emission Inventory for Combustion and
Industrial Sources with New Data from the Residential and Transportation
Sectors, Environ. Sci. Technol., 51, 2821–2829,
https://doi.org/10.1021/acs.est.6b03694, 2017. a
NASA: OWLETS 2018 Data, NASA [data], available at: https://www-air.larc.nasa.gov/cgi-bin/ArcView/owlets.2018, last access: 28 July 2021. a
Nenes, A., Pandis, S. N., Kanakidou, M., Russell, A. G., Song, S., Vasilakos, P., and Weber, R. J.: Aerosol acidity and liquid water content regulate the dry deposition of inorganic reactive nitrogen, Atmos. Chem. Phys., 21, 6023–6033, https://doi.org/10.5194/acp-21-6023-2021, 2021. a, b
NOAA: National Coastal Population Report: Population Trends from 1970 to 2020, available at: https://aambpublicoceanservice.blob.core.windows.net/oceanserviceprod/facts/coastal-population-report.pdf (last access: 30 April 2021), 2013. a
Norman, M., Spirig, C., Wolff, V., Trebs, I., Flechard, C., Wisthaler, A., Schnitzhofer, R., Hansel, A., and Neftel, A.: Intercomparison of ammonia measurement techniques at an intensively managed grassland site (Oensingen, Switzerland), Atmos. Chem. Phys., 9, 2635–2645, https://doi.org/10.5194/acp-9-2635-2009, 2009. a, b
Orsini, D. A., Ma, Y., Sullivan, A., Sierau, B., Baumann, K., and Weber, R. J.:
Refinements to the particle-into-liquid sampler (PILS) for ground and
airborne measurements of water soluble aerosol composition, Atmos. Environ.,
37, 1243–1259, https://doi.org/10.1016/S1352-2310(02)01015-4, 2003. a
Pagans, E., Barrena, R., Font, X., and Sánchez, A.: Ammonia emissions from
the composting of different organic wastes. Dependency on process
temperature, Chemosphere, 62, 1534–1542,
https://doi.org/10.1016/j.chemosphere.2005.06.044, 2006. a
Paulot, F. and Jacob, D. J.: Hidden Cost of U.S. Agricultural Exports:
Particulate Matter from Ammonia Emissions, Environ. Sci. Technol., 48,
903–908, https://doi.org/10.1021/es4034793, 2014. a
Paulot, F., Jacob, D. J., Johnson, M. T., Bell, T. G., Baker, A. R., Keene,
W. C., Lima, I. D., Doney, S. C., and Stock, C. A.: Global oceanic emission
of ammonia: Constraints from seawater and atmospheric observations, Global
Biogeochem. Cy., 29, 1165–1178, https://doi.org/10.1002/2015GB005106, 2015. a, b, c
Paulot, F., Ginoux, P., Cooke, W. F., Donner, L. J., Fan, S., Lin, M.-Y., Mao, J., Naik, V., and Horowitz, L. W.: Sensitivity of nitrate aerosols to ammonia emissions and to nitrate chemistry: implications for present and future nitrate optical depth, Atmos. Chem. Phys., 16, 1459–1477, https://doi.org/10.5194/acp-16-1459-2016, 2016. a
Paulot, F., Paynter, D., Ginoux, P., Naik, V., Whitburn, S., Van Damme, M.,
Clarisse, L., Coheur, P.-F., and Horowitz, L.: Gas-aerosol partitioning of
ammonia in biomass burning plumes: Implications for the interpretation of
spaceborne observations of ammonia and the radiative forcing of ammonium
nitrate, Geophys. Res. Lett., 44, 8084–8093, https://doi.org/10.1002/2017GL074215,
2017. a
Perrino, C., Catrambone, M., Di Bucchianico, A. D. M., and Allegrini, I.:
Gaseous ammonia in the urban area of Rome, Italy and its relationship with
traffic emissions, Atmos. Environ., 36, 5385–5394,
https://doi.org/10.1016/S1352-2310(02)00469-7, 2002. a, b
Pinder, R., Gilliland, A., and Dennis, R.: Environmental impact of atmospheric
NH3 emissions under present and future conditions in the eastern United
States, Geophys. Res. Lett., 35, L12808, https://doi.org/10.1029/2008GL033732, 2008. a
Pinder, R. W., Pekney, N. J., Davidson, C. I., and Adams, P. J.: A
process-based model of ammonia emissions from dairy cows: improved temporal
and spatial resolution, Atmos. Environ., 38, 1357–1365,
https://doi.org/10.1016/j.atmosenv.2003.11.024, 2004a. a
Pinder, R. W., Strader, R., Davidson, C. I., and Adams, P. J.: A temporally and
spatially resolved ammonia emission inventory for dairy cows in the United
States, Atmos. Environ., 38, 3747–3756,
https://doi.org/10.1016/j.atmosenv.2004.04.008, 2004b. a
Pinder, R. W., Adams, P. J., Pandis, S. N., and Gilliland, A. B.: Temporally
resolved ammonia emission inventories: Current estimates, evaluation tools,
and measurement needs, J. Geophys. Res.-Atmos., 111, D16310,
https://doi.org/10.1029/2005JD006603, 2006. a, b
Pinder, R. W., Adams, P. J., and Pandis, S. N.: Ammonia emission controls as a
cost-effective strategy for reducing atmospheric particulate matter in the
eastern United States, Environ. Sci. Technol., 41, 380–386, https://doi.org/10.1021/es060379a, 2007. a, b
Pleim, J. E., Bash, J. O., Walker, J. T., and Cooter, E. J.: Development and
evaluation of an ammonia bidirectional flux parameterization for air quality
models, J. Geophys. Res.-Atmos., 118, 3794–3806, https://doi.org/10.1002/jgrd.50262,
2013. a, b
Poulain, L., Spindler, G., Birmili, W., Plass-Dülmer, C., Wiedensohler, A., and Herrmann, H.: Seasonal and diurnal variations of particulate nitrate and organic matter at the IfT research station Melpitz, Atmos. Chem. Phys., 11, 12579–12599, https://doi.org/10.5194/acp-11-12579-2011, 2011. a
Pozzer, A., Tsimpidi, A. P., Karydis, V. A., de Meij, A., and Lelieveld, J.: Impact of agricultural emission reductions on fine-particulate matter and public health, Atmos. Chem. Phys., 17, 12813–12826, https://doi.org/10.5194/acp-17-12813-2017, 2017. a
Reche, C., Viana, M., Karanasiou, A., Cusack, M., Alastuey, A., Artiñano, B., Revuelta, M. A., López-Mahía, P., Blanco-Heras, G., Rodríguez, S., Sánchez de la Campa, A. M., Fernández-Camacho, R., González-Castanedo, Y., Mantilla, E., Sim Tanh, Y., and Querol, X.: Urban NH3 levels and sources in six major
Spanish cities, Chemosphere, 119, 769–777,
https://doi.org/10.1016/j.chemosphere.2014.07.097, 2015. a
Robarge, W. P., Walker, J. T., McCulloch, R. B., and Murray, G.: Atmospheric
concentrations of ammonia and ammonium at an agricultural site in the
southeast United States, Atmos. Environ., 36, 1661–1674,
https://doi.org/10.1016/S1352-2310(02)00171-1, 2002. a
Schmohl, A., Miklos, A., and Hess, P.: Effects of adsorption–desorption
processes on the response time and accuracy of photoacoustic detection of
ammonia, Appl. Opt., 40, 2571–2578, https://doi.org/10.1364/AO.40.002571, 2001. a
Sickles, J. E. and Shadwick, D. S.: Comparison of particulate sulfate and
nitrate at collocated CASTNET and IMPROVE sites in the eastern US, Atmos.
Environ., 42, 2062–2073, https://doi.org/10.1016/j.atmosenv.2007.11.051, 2008. a
Siefert, R. L., Scudlark, J. R., Potter, A. G., Simonsen, K. A., and Savidge,
K. B.: Characterization of atmospheric ammonia emissions from a commercial
chicken house on the Delmarva Peninsula, Environ. Sci. Technol., 38,
2769–2778, https://doi.org/10.1021/es0345874, 2004. a
Sorooshian, A., Murphy, S. M., Hersey, S., Gates, H., Padro, L. T., Nenes, A., Brechtel, F. J., Jonsson, H., Flagan, R. C., and Seinfeld, J. H.: Comprehensive airborne characterization of aerosol from a major bovine source, Atmos. Chem. Phys., 8, 5489–5520, https://doi.org/10.5194/acp-8-5489-2008, 2008. a
Stein, A., Draxler, R. R., Rolph, G. D., Stunder, B. J., Cohen, M., and Ngan,
F.: NOAA’s HYSPLIT atmospheric transport and dispersion modeling system, B.
Am. Meteorol. Soc., 96, 2059–2077, https://doi.org/10.1175/BAMS-D-14-00110.1, 2015. a
Stelson, A. and Seinfeld, J. H.: Relative humidity and temperature dependence
of the ammonium nitrate dissociation constant, Atmos. Environ., 16, 983–992,
https://doi.org/10.1016/0004-6981(82)90184-6, 1982. a
Stull, R. B.: An Introduction to Boundary Layer Meteorology, vol. 13, Springer
Science & Business Media, the Netherlands, 1988. a
Sullivan, J. T., Berkoff, T., Gronoff, G., Knepp, T., Pippin, M., Allen, D.,
Twigg, L., Swap, R., Tzortziou, M., Thompson, A. M., Stauffer, R. M., Wolfe,
G. M., Flynn, J., Pusede, S. E., Judd, L. M., Moore, W., Baker, B. D.,
Al-Saadi, J., and McGee, T. J.: The Ozone Water–Land Environmental
Transition Study: An Innovative Strategy for Understanding Chesapeake Bay
Pollution Events, B. Am. Meteorol. Soc., 100, 291–306,
https://doi.org/10.1175/BAMS-D-18-0025.1, 2019. a
Sun, K., Tao, L., Miller, D. J., Pan, D., Golston, L. M., Zondlo, M. A.,
Griffin, R. J., Wallace, H. W., Leong, Y. J., Yang, M. M., Zhang, Y.,
Mauzerall, D. L., and Zhu, T.: Vehicle Emissions as an Important Urban
Ammonia Source in the United States and China, Environ. Sci. Technol., 51,
2472–2481, https://doi.org/10.1021/acs.est.6b02805, 2017. a, b
Sutton, M., Dragosits, U., Tang, Y., and Fowler, D.: Ammonia emissions from
non-agricultural sources in the UK, Atmos. Environ., 34, 855–869,
https://doi.org/10.1016/S1352-2310(99)00362-3, 2000. a
Sutton, M. A., Reis, S., Riddick, S. N., Dragosits, U., Nemitz, E., Theobald,
M. R., Tang, Y. S., Braban, C. F., Vieno, M., Dore, A. J., Mitchell, R. F.,
Wanless, S., Daunt, F., Fowler, D., Blackall, T. D., Milford, C., Flechard,
C. R., Loubet, B., Massad, R., Cellier, P., Personne, E., Coheur, P. F.,
Clarisse, L., Van Damme, M., Ngadi, Y., Clerbaux, C., Skjøth, C. A., Geels,
C., Hertel, O., Wichink Kruit, R. J., Pinder, R. W., Bash, J. O., Walker,
J. T., Simpson, D., Horváth, L., Misselbrook, T. H., Bleeker, A., Dentener,
F., and de Vries, W.: Towards a climate-dependent paradigm of ammonia
emission and deposition, Philos. T. Roy. Soc. B, 368, 1–13,
https://doi.org/10.1098/rstb.2013.0166, 2013. a, b, c, d, e
Tsigaridis, K., Daskalakis, N., Kanakidou, M., Adams, P. J., Artaxo, P., Bahadur, R., Balkanski, Y., Bauer, S. E., Bellouin, N., Benedetti, A., Bergman, T., Berntsen, T. K., Beukes, J. P., Bian, H., Carslaw, K. S., Chin, M., Curci, G., Diehl, T., Easter, R. C., Ghan, S. J., Gong, S. L., Hodzic, A., Hoyle, C. R., Iversen, T., Jathar, S., Jimenez, J. L., Kaiser, J. W., Kirkevåg, A., Koch, D., Kokkola, H., Lee, Y. H., Lin, G., Liu, X., Luo, G., Ma, X., Mann, G. W., Mihalopoulos, N., Morcrette, J.-J., Müller, J.-F., Myhre, G., Myriokefalitakis, S., Ng, N. L., O'Donnell, D., Penner, J. E., Pozzoli, L., Pringle, K. J., Russell, L. M., Schulz, M., Sciare, J., Seland, Ø., Shindell, D. T., Sillman, S., Skeie, R. B., Spracklen, D., Stavrakou, T., Steenrod, S. D., Takemura, T., Tiitta, P., Tilmes, S., Tost, H., van Noije, T., van Zyl, P. G., von Salzen, K., Yu, F., Wang, Z., Wang, Z., Zaveri, R. A., Zhang, H., Zhang, K., Zhang, Q., and Zhang, X.: The AeroCom evaluation and intercomparison of organic aerosol in global models, Atmos. Chem. Phys., 14, 10845–10895, https://doi.org/10.5194/acp-14-10845-2014, 2014. a
Turnock, S., Mann, G., Woodhouse, M., Dalvi, M., O'Connor, F., Carslaw, K., and
Spracklen, D.: The impact of changes in cloud water pH on aerosol radiative
forcing, Geophys. Res. Lett., 46, 4039–4048, https://doi.org/10.1029/2019GL082067,
2019. a
USDA: Census of Agriculture, Volume 1, chap. 2, County Level Data, United States Department of Agriculture, Tech.
rep., 2017. a
Valerino, M., Johnson, J., Izumi, J., Orozco, D., Hoff, R., Delgado, R., and
Hennigan, C.: Sources and composition of PM2.5 in the Colorado Front
Range during the DISCOVER-AQ study, J. Geophys. Res.-Atmos., 122, 566–582,
https://doi.org/10.1002/2016JD025830, 2017. a
Van Damme, M., Clarisse, L., Whitburn, S., Hadji-Lazaro, J., Hurtmans, D.,
Clerbaux, C., and Coheur, P.-F.: Industrial and agricultural ammonia point
sources exposed, Nature, 564, 99–103, https://doi.org/10.1038/s41586-018-0747-1, 2018. a, b
von Bobrutzki, K., Braban, C. F., Famulari, D., Jones, S. K., Blackall, T., Smith, T. E. L., Blom, M., Coe, H., Gallagher, M., Ghalaieny, M., McGillen, M. R., Percival, C. J., Whitehead, J. D., Ellis, R., Murphy, J., Mohacsi, A., Pogany, A., Junninen, H., Rantanen, S., Sutton, M. A., and Nemitz, E.: Field inter-comparison of eleven atmospheric ammonia measurement techniques, Atmos. Meas. Tech., 3, 91–112, https://doi.org/10.5194/amt-3-91-2010, 2010. a, b
Vutukuru, S. and Dabdub, D.: Modeling the effects of ship emissions on coastal
air quality: A case study of southern California, Atmos. Environ., 42,
3751–3764, https://doi.org/10.1016/j.atmosenv.2007.12.073, 2008. a
Warner, J., Dickerson, R., Wei, Z., Strow, L. L., Wang, Y., and Liang, Q.:
Increased atmospheric ammonia over the world's major agricultural areas
detected from space, Geophys. Res. Lett., 44, 2875–2884,
https://doi.org/10.1002/2016GL072305, 2017. a, b
Washenfelder, R. A., Attwood, A. R., Brock, C. A., Guo, H., Xu, L., Weber,
R. J., Ng, N. L., Allen, H. M., Ayres, B. R., Baumann, K., Cohen, R. C.,
Draper, D. C., Duffey, K. C., Edgerton, E., Fry, J. L., Hu, W. W., Jimenez,
J. L., Palm, B. B., Romer, P., Stone, E. A., Wooldridge, P. J., and Brown,
S. S.: Biomass burning dominates brown carbon absorption in the rural
southeastern United States, Geophys. Res. Lett., 42, 653–664,
https://doi.org/10.1002/2014GL062444, 2015. a
Weber, R.: Short-term temporal variation in PM2.5 mass and chemical
composition during the Atlanta Supersite Experiment, 1999, J. Air Waste
Manage., 53, 84–91, https://doi.org/10.1080/10473289.2003.10466123, 2003. a
Weber, R. J., Guo, H., Russell, A. G., and Nenes, A.: High aerosol acidity
despite declining atmospheric sulfate concentrations over the past 15 years,
Nat. Geosci., 9, 282–285, https://doi.org/10.1038/ngeo2665, 2016. a
Wittig, A. E., Anderson, N., Khlystov, A. Y., Pandis, S. N., Davidson, C., and
Robinson, A. L.: Pittsburgh air quality study overview, Atmos. Environ., 38,
3107–3125, https://doi.org/10.1016/j.atmosenv.2004.03.003, 2004. a, b
Wolfe, G.: HYSPLITcontrol, GitHub [code], https://github.com/AirChem/HYSPLITcontrol, last access: 28 July 2021. a
Wyers, G., Otjes, R., and Slanina, J.: A continuous-flow denuder for the
measurement of ambient concentrations and surface-exchange fluxes of ammonia,
Atmos. Environ., 27, 2085–2090, https://doi.org/10.1016/0960-1686(93)90280-C, 1993. a, b
Xu, L., Suresh, S., Guo, H., Weber, R. J., and Ng, N. L.: Aerosol characterization over the southeastern United States using high-resolution aerosol mass spectrometry: spatial and seasonal variation of aerosol composition and sources with a focus on organic nitrates, Atmos. Chem. Phys., 15, 7307–7336, https://doi.org/10.5194/acp-15-7307-2015, 2015. a
Fu, X., Wang, T., Zhang, L., Li, Q., Wang, Z., Xia, M., Yun, H., Wang, W., Yu, C., Yue, D., Zhou, Y., Zheng, J., and Han, R.: The significant contribution of HONO to secondary pollutants during a severe winter pollution event in southern China, Atmos. Chem. Phys., 19, 1–14, https://doi.org/10.5194/acp-19-1-2019, 2019.
a
Zhao, B., Wang, S., Wang, J., Fu, J. S., Liu, T., Xu, J., Fu, X., and Hao, J.:
Impact of national NOx and SO2 control policies on particulate
matter pollution in China, Atmos. Environ., 77, 453–463,
https://doi.org/10.1016/j.atmosenv.2013.05.012, 2013. a
Zhu, L., Henze, D., Bash, J., Jeong, G.-R., Cady-Pereira, K., Shephard, M., Luo, M., Paulot, F., and Capps, S.: Global evaluation of ammonia bidirectional exchange and livestock diurnal variation schemes, Atmos. Chem. Phys., 15, 12823–12843, https://doi.org/10.5194/acp-15-12823-2015, 2015. a
Short summary
Measurements of aerosol and gas composition were carried out at a land–water transition site near Baltimore, MD. Gas-phase ammonia concentrations were highly elevated compared to measurements at a nearby inland site. Our analysis reveals that NH2 was from both industrial and agricultural sources. This had a pronounced effect on aerosol chemical composition at the site, most notably contributing to episodic spikes of aerosol nitrate.
Measurements of aerosol and gas composition were carried out at a land–water transition site...
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