Articles | Volume 19, issue 15
https://doi.org/10.5194/acp-19-9681-2019
© Author(s) 2019. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/acp-19-9681-2019
© Author(s) 2019. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Research article
| 
01 Aug 2019
Research article |
| 01 Aug 2019
| 01 Aug 2019
Gas-phase pyrolysis products emitted by prescribed fires in pine forests with a shrub understory in the southeastern United States
Nicole K. Scharko
Pacific Northwest National Laboratories, Richland, WA, USA
Ashley M. Oeck
Pacific Northwest National Laboratories, Richland, WA, USA
Tanya L. Myers
Pacific Northwest National Laboratories, Richland, WA, USA
Russell G. Tonkyn
Pacific Northwest National Laboratories, Richland, WA, USA
Catherine A. Banach
Pacific Northwest National Laboratories, Richland, WA, USA
Stephen P. Baker
USDA Forest Service, Rocky Mountain Research Station, Missoula, MT,
USA
Emily N. Lincoln
USDA Forest Service, Rocky Mountain Research Station, Missoula, MT,
USA
Joey Chong
USDA Forest Service, Pacific Southwest Research Station, Riverside,
CA, USA
Bonni M. Corcoran
USDA Forest Service, Pacific Southwest Research Station, Riverside,
CA, USA
Gloria M. Burke
USDA Forest Service, Pacific Southwest Research Station, Riverside,
CA, USA
Roger D. Ottmar
USDA Forest Service, Pacific Northwest Research Station, Seattle WA,
USA
Joseph C. Restaino
School of Environmental and Forest Sciences, University of Washington,
Seattle WA, USA
David R. Weise
USDA Forest Service, Pacific Southwest Research Station, Riverside,
CA, USA
Timothy J. Johnson
CORRESPONDING AUTHOR
Pacific Northwest National Laboratories, Richland, WA, USA
Related authors
No articles found.
Catherine A. Banach, Ashley M. Bradley, Russell G. Tonkyn, Olivia N. Williams, Joey Chong, David R. Weise, Tanya L. Myers, and Timothy J. Johnson
Atmos. Meas. Tech., 14, 2359–2376, https://doi.org/10.5194/amt-14-2359-2021, https://doi.org/10.5194/amt-14-2359-2021, 2021
Short summary
Short summary
We have developed a novel method to identify and characterize the gases emitted in biomass burning fires in a time-resolved fashion. Using time-resolved infrared spectroscopy combined with time-resolved thermal imaging in a wind tunnel, we were able to capture the gas-phase dynamics of the burning of plants native to the southeastern United States.
Nishit J. Shetty, Apoorva Pandey, Stephen Baker, Wei Min Hao, and Rajan K. Chakrabarty
Atmos. Chem. Phys., 19, 8817–8830, https://doi.org/10.5194/acp-19-8817-2019, https://doi.org/10.5194/acp-19-8817-2019, 2019
Short summary
Short summary
We investigated biases in particle-phase absorption coefficients for organic aerosol from bulk-phase absorbance measurements of solvent extracts in the visible spectrum. These biases were systematically studied as a function of organic-to-total carbon mass ratios and aerosol single scattering albedo. A linear correlation between SSA and OC / TC ratios was observed. Differences in the absorption Ångström exponents from bulk- and particle-phase measurements were also investigated.
Nicole K. Scharko, Ashley M. Oeck, Russell G. Tonkyn, Stephen P. Baker, Emily N. Lincoln, Joey Chong, Bonni M. Corcoran, Gloria M. Burke, David R. Weise, Tanya L. Myers, Catherine A. Banach, David W. T. Griffith, and Timothy J. Johnson
Atmos. Meas. Tech., 12, 763–776, https://doi.org/10.5194/amt-12-763-2019, https://doi.org/10.5194/amt-12-763-2019, 2019
Short summary
Short summary
We report five species (naphthalene, methyl nitrite, allene, acrolein and acetaldehyde) that were detected in biomass burning fires that had been seen before in burn studies, but are reported for the first time when using infrared spectroscopy for detection.
R. V. Kochanov, I. E. Gordon, L. S. Rothman, S. W. Sharpe, T. J. Johnson, and R. L. Sams
Clim. Past, 11, 1097–1105, https://doi.org/10.5194/cp-11-1097-2015, https://doi.org/10.5194/cp-11-1097-2015, 2015
Short summary
Short summary
In the article Clim Past 10, 1779 (2014), the HITRAN2012 database was employed to evaluate the radiative forcing of 28 Archean gases. The authors claimed that for NO2, H2O2, C2H4, CH3OH, and CH3Br there are severe disagreements between cross sections generated from the HITRAN line-by-line data and those of the PNNL experimental database. In this work we show that the differences are not nearly at the scale suggested by the authors, and their conclusions about these gases and HO2 are not correct.
M. J. Alvarado, C. R. Lonsdale, R. J. Yokelson, S. K. Akagi, H. Coe, J. S. Craven, E. V. Fischer, G. R. McMeeking, J. H. Seinfeld, T. Soni, J. W. Taylor, D. R. Weise, and C. E. Wold
Atmos. Chem. Phys., 15, 6667–6688, https://doi.org/10.5194/acp-15-6667-2015, https://doi.org/10.5194/acp-15-6667-2015, 2015
Short summary
Short summary
Being able to understand and simulate the chemical evolution of biomass burning smoke plumes under a wide variety of conditions is a critical part of forecasting the impact of these fires on air quality, atmospheric composition, and climate. Here we use an improved model of this chemistry to simulate the evolution of ozone and secondary organic aerosol within a young biomass burning smoke plume from the Williams prescribed burn in chaparral, which was sampled over California in November 2009.
C. S. Brauer, T. A. Blake, A. B. Guenther, S. W. Sharpe, R. L. Sams, and T. J. Johnson
Atmos. Meas. Tech., 7, 3839–3847, https://doi.org/10.5194/amt-7-3839-2014, https://doi.org/10.5194/amt-7-3839-2014, 2014
S. K. Akagi, I. R. Burling, A. Mendoza, T. J. Johnson, M. Cameron, D. W. T. Griffith, C. Paton-Walsh, D. R. Weise, J. Reardon, and R. J. Yokelson
Atmos. Chem. Phys., 14, 199–215, https://doi.org/10.5194/acp-14-199-2014, https://doi.org/10.5194/acp-14-199-2014, 2014
S. K. Akagi, R. J. Yokelson, I. R. Burling, S. Meinardi, I. Simpson, D. R. Blake, G. R. McMeeking, A. Sullivan, T. Lee, S. Kreidenweis, S. Urbanski, J. Reardon, D. W. T. Griffith, T. J. Johnson, and D. R. Weise
Atmos. Chem. Phys., 13, 1141–1165, https://doi.org/10.5194/acp-13-1141-2013, https://doi.org/10.5194/acp-13-1141-2013, 2013
R. J. Yokelson, I. R. Burling, J. B. Gilman, C. Warneke, C. E. Stockwell, J. de Gouw, S. K. Akagi, S. P. Urbanski, P. Veres, J. M. Roberts, W. C. Kuster, J. Reardon, D. W. T. Griffith, T. J. Johnson, S. Hosseini, J. W. Miller, D. R. Cocker III, H. Jung, and D. R. Weise
Atmos. Chem. Phys., 13, 89–116, https://doi.org/10.5194/acp-13-89-2013, https://doi.org/10.5194/acp-13-89-2013, 2013
Related subject area
Subject: Gases | Research Activity: Field Measurements | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Measurement report: Molecular-level investigation of atmospheric cluster ions at the tropical high-altitude research station Chacaltaya (5240 m a.s.l.) in the Bolivian Andes
Observations of biogenic volatile organic compounds over a mixed temperate forest during the summer to autumn transition
Unexpectedly high concentrations of atmospheric mercury species in Lhasa, the largest city in the Tibetan Plateau
Real-time measurements of non-methane volatile organic compounds in the central Indo-Gangetic basin, Lucknow, India: source characterisation and their role in O3 and secondary organic aerosol formation
Measurement report: Production and loss of atmospheric formaldehyde at a suburban site of Shanghai in summertime
Measurement report: Volatile organic compound characteristics of the different land-use types in Shanghai: spatiotemporal variation, source apportionment and impact on secondary formations of ozone and aerosol
O3–precursor relationship over multiple patterns of timescale: a case study in Zibo, Shandong Province, China
High emission rates and strong temperature response make boreal wetlands a large source of isoprene and terpenes
Elucidate the formation mechanism of particulate nitrate based on direct radical observations in the Yangtze River Delta summer 2019
Pandemic restrictions in 2020 highlight the significance of non-road NOx sources in central London
Measurement report: Emission factors of NH3 and NHx for wildfires and agricultural fires in the United States
Experimental chemical budgets of OH, HO2, and RO2 radicals in rural air in western Germany during the JULIAC campaign 2019
Chemical and dynamical identification of emission outflows during the HALO campaign EMeRGe in Europe and Asia
Flaring efficiencies and NOx emission ratios measured for offshore oil and gas facilities in the North Sea
Measurement report: Long-range transport and the fate of dimethyl sulfide oxidation products in the free troposphere derived from observations at the high-altitude research station Chacaltaya (5240 m a.s.l.) in the Bolivian Andes
Snowpack nitrate photolysis drives the summertime atmospheric nitrous acid (HONO) budget in coastal Antarctica
Formaldehyde and hydroperoxide distribution around the Arabian Peninsula – evaluation of EMAC model results with ship-based measurements
Heterogeneity and chemical reactivity of the remote troposphere defined by aircraft measurements – corrected
Fundamental oxidation processes in the remote marine atmosphere investigated using the NO–NO2–O3 photostationary state
Emission factors and evolution of SO2 measured from biomass burning in wildfires and agricultural fires
Chemical identification of new particle formation and growth precursors through positive matrix factorization of ambient ion measurements
The unexpected high frequency of nocturnal surface ozone enhancement events over China: characteristics and mechanisms
Source apportionment of VOCs, IVOCs and SVOCs by positive matrix factorization in suburban Livermore, California
Measurement report: Intra- and interannual variability and source apportionment of volatile organic compounds during 2018–2020 in Zhengzhou, central China
Formation and impacts of nitryl chloride in Pearl River Delta
Multidecadal increases in global tropospheric ozone derived from ozonesonde and surface site observations: can models reproduce ozone trends?
What caused ozone pollution during the 2022 Shanghai lockdown? Insights from ground and satellite observations
Ammonium adduct chemical ionization to investigate anthropogenic oxygenated gas-phase organic compounds in urban air
Atmospheric biogenic volatile organic compounds in the Alaskan Arctic tundra: constraints from measurements at Toolik Field Station
Characteristics of Negative Cluster Ions in an Urban Environment
Are dense networks of low-cost nodes really useful for monitoring air pollution? A case study in Staffordshire
Technical note: Northern midlatitude baseline ozone – long-term changes and the COVID-19 impact
Quantifying the importance of vehicle ammonia emissions in an urban area of northeastern USA utilizing nitrogen isotopes
Seasonal variation in nitryl chloride and its relation to gas-phase precursors during the JULIAC campaign in Germany
Radical chemistry in the Pearl River Delta: observations and modeling of OH and HO2 radicals in Shenzhen in 2018
Reconciling the total carbon budget for boreal forest wildfire emissions using airborne observations
Summer variability of the atmospheric NO2 : NO ratio at Dome C on the East Antarctic Plateau
Measurement report: Ambient volatile organic compound (VOC) pollution in urban Beijing: characteristics, sources, and implications for pollution control
Mass spectrometric measurements of ambient ions and estimation of gaseous sulfuric acid in the free troposphere and lowermost stratosphere during the CAFE-EU/BLUESKY campaign
Springtime nitrogen oxides and tropospheric ozone in Svalbard: results from the measurement station network
Measurement report: Observations of long-lived volatile organic compounds from the 2019–2020 Australian wildfires during the COALA campaign
Composition and reactivity of volatile organic compounds in the South Coast Air Basin and San Joaquin Valley of California
Analysis of regional CO2 contributions at the high Alpine observatory Jungfraujoch by means of atmospheric transport simulations and δ13C
Variations and sources of volatile organic compounds (VOCs) in urban region: insights from measurements on a tall tower
Tropical peat fire emissions: 2019 field measurements in Sumatra and Borneo and synthesis with previous studies
Sulfuric acid in the Amazon basin: measurements and evaluation of existing sulfuric acid proxies
Seasonal variation in oxygenated organic molecules in urban Beijing and their contribution to secondary organic aerosol
Oxygenated volatile organic compounds (VOCs) as significant but varied contributors to VOC emissions from vehicles
The impacts of wildfires on ozone production and boundary layer dynamics in California's Central Valley
Distribution of hydrogen peroxide over Europe during the BLUESKY aircraft campaign
Qiaozhi Zha, Wei Huang, Diego Aliaga, Otso Peräkylä, Liine Heikkinen, Alkuin Maximilian Koenig, Cheng Wu, Joonas Enroth, Yvette Gramlich, Jing Cai, Samara Carbone, Armin Hansel, Tuukka Petäjä, Markku Kulmala, Douglas Worsnop, Victoria Sinclair, Radovan Krejci, Marcos Andrade, Claudia Mohr, and Federico Bianchi
Atmos. Chem. Phys., 23, 4559–4576, https://doi.org/10.5194/acp-23-4559-2023, https://doi.org/10.5194/acp-23-4559-2023, 2023
Short summary
Short summary
We investigate the chemical composition of atmospheric cluster ions from January to May 2018 at the high-altitude research station Chacaltaya (5240 m a.s.l.) in the Bolivian Andes. With state-of-the-art mass spectrometers and air mass history analysis, the measured cluster ions exhibited distinct diurnal and seasonal patterns, some of which contributed to new particle formation. Our study will improve the understanding of atmospheric ions and their role in high-altitude new particle formation.
Michael P. Vermeuel, Gordon A. Novak, Delaney B. Kilgour, Megan S. Claflin, Brian M. Lerner, Amy M. Trowbridge, Jonathan Thom, Patricia A. Cleary, Ankur R. Desai, and Timothy H. Bertram
Atmos. Chem. Phys., 23, 4123–4148, https://doi.org/10.5194/acp-23-4123-2023, https://doi.org/10.5194/acp-23-4123-2023, 2023
Short summary
Short summary
Reactive carbon species emitted from natural sources such as forests play an important role in the chemistry of the atmosphere. Predictions of these emissions are based on plant responses during the growing season and do not consider potential effects from seasonal changes. To address this, we made measurements of reactive carbon over a forest during the summer to autumn transition. We learned that observed concentrations and emissions for some key species are larger than model predictions.
Huiming Lin, Yindong Tong, Long Chen, Chenghao Yu, Zhaohan Chu, Qianru Zhang, Xiufeng Yin, Qianggong Zhang, Shichang Kang, Junfeng Liu, James Schauer, Benjamin de Foy, and Xuejun Wang
Atmos. Chem. Phys., 23, 3937–3953, https://doi.org/10.5194/acp-23-3937-2023, https://doi.org/10.5194/acp-23-3937-2023, 2023
Short summary
Short summary
Lhasa is the largest city in the Tibetan Plateau, and its atmospheric mercury concentrations represent the highest level of pollution in this region. Unexpectedly high concentrations of atmospheric mercury species were found. Combined with the trajectory analysis, the high atmospheric mercury concentrations may have originated from external long-range transport. Local sources, especially special mercury-related sources, are important factors influencing the variability of atmospheric mercury.
Vaishali Jain, Nidhi Tripathi, Sachchida N. Tripathi, Mansi Gupta, Lokesh K. Sahu, Vishnu Murari, Sreenivas Gaddamidi, Ashutosh K. Shukla, and Andre S. H. Prevot
Atmos. Chem. Phys., 23, 3383–3408, https://doi.org/10.5194/acp-23-3383-2023, https://doi.org/10.5194/acp-23-3383-2023, 2023
Short summary
Short summary
This research chemically characterises 173 different NMVOCs (non-methane volatile organic compounds) measured in real time for three seasons in the city of the central Indo-Gangetic basin of India, Lucknow. Receptor modelling is used to analyse probable sources of NMVOCs and their crucial role in forming ozone and secondary organic aerosols. It is observed that vehicular emissions and solid fuel combustion are the highest contributors to the emission of primary and secondary NMVOCs.
Yizhen Wu, Juntao Huo, Gan Yang, Yuwei Wang, Lihong Wang, Shijian Wu, Lei Yao, Qingyan Fu, and Lin Wang
Atmos. Chem. Phys., 23, 2997–3014, https://doi.org/10.5194/acp-23-2997-2023, https://doi.org/10.5194/acp-23-2997-2023, 2023
Short summary
Short summary
Based on a field campaign in a suburban area of Shanghai during summer 2021, we calculated formaldehyde (HCHO) production rates from 24 volatile organic compounds (VOCs). In addition, HCHO photolysis, reactions with OH radicals, and dry deposition were considered for the estimation of HCHO loss rates. Our results reveal the key precursors of HCHO and suggest that HCHO wet deposition may be an important loss term on cloudy and rainy days, which needs to be further investigated.
Yu Han, Tao Wang, Rui Li, Hongbo Fu, Yusen Duan, Song Gao, Liwu Zhang, and Jianmin Chen
Atmos. Chem. Phys., 23, 2877–2900, https://doi.org/10.5194/acp-23-2877-2023, https://doi.org/10.5194/acp-23-2877-2023, 2023
Short summary
Short summary
Limited knowledge is available on volatile organic compound (VOC) multi-site research of different land-use types at city level. This study performed a concurrent multi-site observation campaign on the three typical land-use types of Shanghai, East China. The results showed that concentrations, sources and ozone and secondary organic aerosol formation potentials of VOCs varied with the land-use types.
Zhensen Zheng, Kangwei Li, Bo Xu, Jianping Dou, Liming Li, Guotao Zhang, Shijie Li, Chunmei Geng, Wen Yang, Merched Azzi, and Zhipeng Bai
Atmos. Chem. Phys., 23, 2649–2665, https://doi.org/10.5194/acp-23-2649-2023, https://doi.org/10.5194/acp-23-2649-2023, 2023
Short summary
Short summary
Previous box model studies applied different timescales of observational datasets to identify the O3–precursor relationship, but there is a lack of comparison among these different timescales regarding the impact of O3 formation chemistry. Through a case study at Zibo in China, we find that the O3 formation regime showed overall consistency but non-negligible variability among various patterns of timescale. This would be complementary in developing more accurate O3 pollution control strategies.
Lejish Vettikkat, Pasi Miettinen, Angela Buchholz, Pekka Rantala, Hao Yu, Simon Schallhart, Tuukka Petäjä, Roger Seco, Elisa Männistö, Markku Kulmala, Eeva-Stiina Tuittila, Alex B. Guenther, and Siegfried Schobesberger
Atmos. Chem. Phys., 23, 2683–2698, https://doi.org/10.5194/acp-23-2683-2023, https://doi.org/10.5194/acp-23-2683-2023, 2023
Short summary
Short summary
Wetlands cover a substantial fraction of the land mass in the northern latitudes, from northern Europe to Siberia and Canada. Yet, their isoprene and terpene emissions remain understudied. Here, we used a state-of-the-art measurement technique to quantify ecosystem-scale emissions from a boreal wetland during an unusually warm spring/summer. We found that the emissions from this wetland were (a) higher and (b) even more strongly dependent on temperature than commonly thought.
Tianyu Zhai, Keding Lu, Haichao Wang, Shengrong Lou, Xiaorui Chen, Renzhi Hu, and Yuanhang Zhang
Atmos. Chem. Phys., 23, 2379–2391, https://doi.org/10.5194/acp-23-2379-2023, https://doi.org/10.5194/acp-23-2379-2023, 2023
Short summary
Short summary
Particulate nitrate is a growing issue in air pollution. Based on comprehensive field measurement, we show heavy nitrate pollution in eastern China in summer. OH reacting with NO2 at daytime dominates nitrate formation on clean days, while N2O5 hydrolysis largely enhances and become comparable with that of OH reacting with O2 on polluted days (67.2 % and 30.2 %). Model simulation indicates that VOC : NOx = 2 : 1 is effective in mitigating the O3 and nitrate pollution coordinately.
Samuel J. Cliff, Will Drysdale, James D. Lee, Carole Helfter, Eiko Nemitz, Stefan Metzger, and Janet F. Barlow
Atmos. Chem. Phys., 23, 2315–2330, https://doi.org/10.5194/acp-23-2315-2023, https://doi.org/10.5194/acp-23-2315-2023, 2023
Short summary
Short summary
Emissions of nitrogen oxides (NOx) to the atmosphere are an ongoing air quality issue. This study directly measures emissions of NOx and carbon dioxide from a tall tower in central London during the coronavirus pandemic. It was found that transport NOx emissions had reduced by >73 % since 2017 as a result of air quality policy and reduced congestion during coronavirus restrictions. During this period, central London was thought to be dominated by point-source heat and power generation emissions.
Laura Tomsche, Felix Piel, Tomas Mikoviny, Claus J. Nielsen, Hongyu Guo, Pedro Campuzano-Jost, Benjamin A. Nault, Melinda K. Schueneman, Jose L. Jimenez, Hannah Halliday, Glenn Diskin, Joshua P. DiGangi, John B. Nowak, Elizabeth B. Wiggins, Emily Gargulinski, Amber J. Soja, and Armin Wisthaler
Atmos. Chem. Phys., 23, 2331–2343, https://doi.org/10.5194/acp-23-2331-2023, https://doi.org/10.5194/acp-23-2331-2023, 2023
Short summary
Short summary
Ammonia (NH3) is an important trace gas in the atmosphere and fires are among the poorly investigated sources. During the 2019 Fire Influence on Regional to Global Environments and Air Quality (FIREX-AQ) aircraft campaign, we measured gaseous NH3 and particulate ammonium (NH4+) in smoke plumes emitted from 6 wildfires in the Western US and 66 small agricultural fires in the Southeastern US. We herein present a comprehensive set of emission factors of NH3 and NHx, where NHx = NH3 + NH4+.
Changmin Cho, Hendrik Fuchs, Andreas Hofzumahaus, Frank Holland, William J. Bloss, Birger Bohn, Hans-Peter Dorn, Marvin Glowania, Thorsten Hohaus, Lu Liu, Paul S. Monks, Doreen Niether, Franz Rohrer, Roberto Sommariva, Zhaofeng Tan, Ralf Tillmann, Astrid Kiendler-Scharr, Andreas Wahner, and Anna Novelli
Atmos. Chem. Phys., 23, 2003–2033, https://doi.org/10.5194/acp-23-2003-2023, https://doi.org/10.5194/acp-23-2003-2023, 2023
Short summary
Short summary
With this study, we investigated the processes leading to the formation, destruction, and recycling of radicals for four seasons in a rural environment. Complete knowledge of their chemistry is needed if we are to predict the formation of secondary pollutants from primary emissions. The results highlight a still incomplete understanding of the paths leading to the formation of the OH radical, which has been observed in several other environments as well and needs to be further investigated.
Eric Förster, Harald Bönisch, Marco Neumaier, Florian Obersteiner, Andreas Zahn, Andreas Hilboll, Anna B. Kalisz Hedegaard, Nikos Daskalakis, Alexandros Panagiotis Poulidis, Mihalis Vrekoussis, Michael Lichtenstern, and Peter Braesicke
Atmos. Chem. Phys., 23, 1893–1918, https://doi.org/10.5194/acp-23-1893-2023, https://doi.org/10.5194/acp-23-1893-2023, 2023
Short summary
Short summary
The airborne megacity campaign EMeRGe provided an unprecedented amount of trace gas measurements. We combine measured volatile organic compounds (VOCs) with trajectory-modelled emission uptakes to identify potential source regions of pollution. We also characterise the chemical fingerprints (e.g. biomass burning and anthropogenic signatures) of the probed air masses to corroborate the contributing source regions. Our approach is the first large-scale study of VOCs originating from megacities.
Jacob T. Shaw, Amy Foulds, Shona Wilde, Patrick Barker, Freya A. Squires, James Lee, Ruth Purvis, Ralph Burton, Ioana Colfescu, Stephen Mobbs, Samuel Cliff, Stéphane J.-B. Bauguitte, Stuart Young, Stefan Schwietzke, and Grant Allen
Atmos. Chem. Phys., 23, 1491–1509, https://doi.org/10.5194/acp-23-1491-2023, https://doi.org/10.5194/acp-23-1491-2023, 2023
Short summary
Short summary
Flaring is used by the oil and gas sector to dispose of unwanted natural gas or for safety. However, few studies have assessed the efficiency with which the gas is combusted. We sampled flaring emissions from offshore facilities in the North Sea. Average measured flaring efficiencies were ~ 98 % but with a skewed distribution, including many flares of lower efficiency. NOx and ethane emissions were also measured. Inefficient flaring practices could be a target for mitigating carbon emissions.
Wiebke Scholz, Jiali Shen, Diego Aliaga, Cheng Wu, Samara Carbone, Isabel Moreno, Qiaozhi Zha, Wei Huang, Liine Heikkinen, Jean Luc Jaffrezo, Gaelle Uzu, Eva Partoll, Markus Leiminger, Fernando Velarde, Paolo Laj, Patrick Ginot, Paolo Artaxo, Alfred Wiedensohler, Markku Kulmala, Claudia Mohr, Marcos Andrade, Victoria Sinclair, Federico Bianchi, and Armin Hansel
Atmos. Chem. Phys., 23, 895–920, https://doi.org/10.5194/acp-23-895-2023, https://doi.org/10.5194/acp-23-895-2023, 2023
Short summary
Short summary
Dimethyl sulfide (DMS), emitted from the ocean, is the most abundant biogenic sulfur emission into the atmosphere. OH radicals, among others, can oxidize DMS to sulfuric and methanesulfonic acid, which are relevant for aerosol formation. We quantified DMS and nearly all DMS oxidation products with novel mass spectrometric instruments for gas and particle phase at the high mountain station Chacaltaya (5240 m a.s.l.) in the Bolivian Andes in free tropospheric air after long-range transport.
Amelia M. H. Bond, Markus M. Frey, Jan Kaiser, Jörg Kleffmann, Anna E. Jones, and Freya A. Squires
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2022-845, https://doi.org/10.5194/acp-2022-845, 2023
Revised manuscript accepted for ACP
Short summary
Short summary
Atmospheric nitrous acid (HONO) amount fractions measured at Halley Research Station, Antarctica, were found to be low. Vertical fluxes of HONO from the snow were also measured and agree with the estimated HONO production rate from photolysis of snow nitrate. In simple box model of HONO sources and sinks there was good agreement between the measured flux and amount fraction. HONO was found to be an important OH radical source at Halley.
Dirk Dienhart, Bettina Brendel, John N. Crowley, Philipp G. Eger, Hartwig Harder, Monica Martinez, Andrea Pozzer, Roland Rohloff, Jan Schuladen, Sebastian Tauer, David Walter, Jos Lelieveld, and Horst Fischer
Atmos. Chem. Phys., 23, 119–142, https://doi.org/10.5194/acp-23-119-2023, https://doi.org/10.5194/acp-23-119-2023, 2023
Short summary
Short summary
Formaldehyde and hydroperoxide measurements were performed in the marine boundary layer around the Arabian Peninsula and highlight the Suez Canal and Arabian (Persian) Gulf as a hotspot of photochemical air pollution. A comparison with the EMAC model shows that the formaldehyde results match within a factor of 2, while hydrogen peroxide was overestimated by more than a factor of 5, which revealed enhanced HOx (OH+HO2) radicals in the simulation and an underestimation of dry deposition velocites.
Hao Guo, Clare M. Flynn, Michael J. Prather, Sarah A. Strode, Stephen D. Steenrod, Louisa Emmons, Forrest Lacey, Jean-Francois Lamarque, Arlene M. Fiore, Gus Correa, Lee T. Murray, Glenn M. Wolfe, Jason M. St. Clair, Michelle Kim, John Crounse, Glenn Diskin, Joshua DiGangi, Bruce C. Daube, Roisin Commane, Kathryn McKain, Jeff Peischl, Thomas B. Ryerson, Chelsea Thompson, Thomas F. Hanisco, Donald Blake, Nicola J. Blake, Eric C. Apel, Rebecca S. Hornbrook, James W. Elkins, Eric J. Hintsa, Fred L. Moore, and Steven C. Wofsy
Atmos. Chem. Phys., 23, 99–117, https://doi.org/10.5194/acp-23-99-2023, https://doi.org/10.5194/acp-23-99-2023, 2023
Short summary
Short summary
We have prepared a unique and unusual result from the recent ATom aircraft mission: a measurement-based derivation of the production and loss rates of ozone and methane over the ocean basins. These are the key products of chemistry models used in assessments but have thus far lacked observational metrics. It also shows the scales of variability of atmospheric chemical rates and provides a major challenge to the atmospheric models.
Simone T. Andersen, Beth S. Nelson, Katie A. Read, Shalini Punjabi, Luis Neves, Matthew J. Rowlinson, James Hopkins, Tomás Sherwen, Lisa K. Whalley, James D. Lee, and Lucy J. Carpenter
Atmos. Chem. Phys., 22, 15747–15765, https://doi.org/10.5194/acp-22-15747-2022, https://doi.org/10.5194/acp-22-15747-2022, 2022
Short summary
Short summary
The cycling of NO and NO2 is important to understand to be able to predict O3 concentrations in the atmosphere. We have used long-term measurements from the Cape Verde Atmospheric Observatory together with model outputs to investigate the cycling of nitrogen oxide (NO) and nitrogen dioxide (NO2) in very clean marine air. This study shows that we understand the processes occurring in very clean air, but with small amounts of pollution in the air, known chemistry cannot explain what is observed.
Pamela S. Rickly, Hongyu Guo, Pedro Campuzano-Jost, Jose L. Jimenez, Glenn M. Wolfe, Ryan Bennett, Ilann Bourgeois, John D. Crounse, Jack E. Dibb, Joshua P. DiGangi, Glenn S. Diskin, Maximilian Dollner, Emily M. Gargulinski, Samuel R. Hall, Hannah S. Halliday, Thomas F. Hanisco, Reem A. Hannun, Jin Liao, Richard Moore, Benjamin A. Nault, John B. Nowak, Jeff Peischl, Claire E. Robinson, Thomas Ryerson, Kevin J. Sanchez, Manuel Schöberl, Amber J. Soja, Jason M. St. Clair, Kenneth L. Thornhill, Kirk Ullmann, Paul O. Wennberg, Bernadett Weinzierl, Elizabeth B. Wiggins, Edward L. Winstead, and Andrew W. Rollins
Atmos. Chem. Phys., 22, 15603–15620, https://doi.org/10.5194/acp-22-15603-2022, https://doi.org/10.5194/acp-22-15603-2022, 2022
Short summary
Short summary
Biomass burning sulfur dioxide (SO2) emission factors range from 0.27–1.1 g kg-1 C. Biomass burning SO2 can quickly form sulfate and organosulfur, but these pathways are dependent on liquid water content and pH. Hydroxymethanesulfonate (HMS) appears to be directly emitted from some fire sources but is not the sole contributor to the organosulfur signal. It is shown that HMS and organosulfur chemistry may be an important S(IV) reservoir with the fate dependent on the surrounding conditions.
Daniel John Katz, Aroob Abdelhamid, Harald Stark, Manjula R. Canagaratna, Douglas R. Worsnop, and Eleanor C. Browne
EGUsphere, https://doi.org/10.5194/egusphere-2022-1318, https://doi.org/10.5194/egusphere-2022-1318, 2022
Short summary
Short summary
Ambient ion chemical composition measurements provide insight into trace gases that are precursors for the formation and growth of new aerosol particles. We use a new data analysis approach to increase the chemical information from these measurements. We analyze results from an agricultural region – an understudied land use type that is ~41 % of global land use – and find that the composition of gases important for aerosol formation and growth differ significantly from those in other ecosystems.
Cheng He, Xiao Lu, Haolin Wang, Haichao Wang, Yan Li, Guowen He, Yuanping He, Yurun Wang, Youlang Zhang, Yiming Liu, Qi Fan, and Shaojia Fan
Atmos. Chem. Phys., 22, 15243–15261, https://doi.org/10.5194/acp-22-15243-2022, https://doi.org/10.5194/acp-22-15243-2022, 2022
Short summary
Short summary
We report that nocturnal ozone enhancement (NOE) events are observed at a high annual frequency of 41 % over 800 sites in China in 2014–2019 (about 50 % higher than that over Europe or the US). High daytime ozone provides a rich ozone source in the nighttime residual layer, determining the overall high frequency of NOE events in China, and enhanced atmospheric mixing then triggers NOE events by allowing the ozone-rich air in the residual layer to be mixed into the nighttime boundary layer.
Rebecca A. Wernis, Nathan M. Kreisberg, Robert J. Weber, Greg T. Drozd, and Allen H. Goldstein
Atmos. Chem. Phys., 22, 14987–15019, https://doi.org/10.5194/acp-22-14987-2022, https://doi.org/10.5194/acp-22-14987-2022, 2022
Short summary
Short summary
We measured volatile and intermediate-volatility gases and semivolatile gas- and particle-phase compounds in the atmosphere during an 11 d period in a Bay Area suburb. We separated compounds based on variability in time to arrive at 13 distinct sources. Some compounds emitted from plants are found in greater quantities as fragrance compounds in consumer products. The wide volatility range of these measurements enables the construction of more complete source profiles.
Shijie Yu, Shenbo Wang, Ruixin Xu, Dong Zhang, Meng Zhang, Fangcheng Su, Xuan Lu, Xiao Li, Ruiqin Zhang, and Lingling Wang
Atmos. Chem. Phys., 22, 14859–14878, https://doi.org/10.5194/acp-22-14859-2022, https://doi.org/10.5194/acp-22-14859-2022, 2022
Short summary
Short summary
In this study, the hourly data of 57 VOC species were collected during 2018–2020 at an urban site in Zhengzhou, China. The research of concentrations, source apportionment, and atmospheric environmental implications clearly elucidated the differences in major reactants observed in different seasons and years. Therefore, the control strategy should focus on key species and sources among interannual and seasonal variations. The results can provide references to develop control strategies.
Haichao Wang, Bin Yuan, E Zheng, Xiaoxiao Zhang, Jie Wang, Keding Lu, Chenshuo Ye, Lei Yang, Shan Huang, Weiwei Hu, Suxia Yang, Yuwen Peng, Jipeng Qi, Sihang Wang, Xianjun He, Yubin Chen, Tiange Li, Wenjie Wang, Yibo Huangfu, Xiaobing Li, Mingfu Cai, Xuemei Wang, and Min Shao
Atmos. Chem. Phys., 22, 14837–14858, https://doi.org/10.5194/acp-22-14837-2022, https://doi.org/10.5194/acp-22-14837-2022, 2022
Short summary
Short summary
We present intensive field measurement of ClNO2 in the Pearl River Delta in 2019. Large variation in the level, formation, and atmospheric impacts of ClNO2 was found in different air masses. ClNO2 formation was limited by the particulate chloride (Cl−) and aerosol surface area. Our results reveal that Cl− originated from various anthropogenic emissions rather than sea sources and show minor contribution to the O3 pollution and photochemistry.
Amy Christiansen, Loretta J. Mickley, Junhua Liu, Luke D. Oman, and Lu Hu
Atmos. Chem. Phys., 22, 14751–14782, https://doi.org/10.5194/acp-22-14751-2022, https://doi.org/10.5194/acp-22-14751-2022, 2022
Short summary
Short summary
Understanding tropospheric ozone trends is crucial for accurate predictions of future air quality and climate, but drivers of trends are not well understood. We analyze global tropospheric ozone trends since 1980 using ozonesonde and surface measurements, and we evaluate two models for their ability to reproduce trends. We find observational evidence of increasing tropospheric ozone, but models underestimate these increases. This hinders our ability to estimate ozone radiative forcing.
Yue Tan and Tao Wang
Atmos. Chem. Phys., 22, 14455–14466, https://doi.org/10.5194/acp-22-14455-2022, https://doi.org/10.5194/acp-22-14455-2022, 2022
Short summary
Short summary
We present a timely analysis of the effects of the recent lockdown in Shanghai on ground-level ozone (O3). Despite a huge reduction in human activity, O3 concentrations frequently exceeded the O3 air quality standard during the 2-month lockdown, implying that future emission reductions similar to those that occurred during the lockdown will not be sufficient to eliminate O3 pollution in many urban areas without the imposition of additional VOC controls or substantial decreases in NOx emissions.
Peeyush Khare, Jordan E. Krechmer, Jo E. Machesky, Tori Hass-Mitchell, Cong Cao, Junqi Wang, Francesca Majluf, Felipe Lopez-Hilfiker, Sonja Malek, Will Wang, Karl Seltzer, Havala O. T. Pye, Roisin Commane, Brian C. McDonald, Ricardo Toledo-Crow, John E. Mak, and Drew R. Gentner
Atmos. Chem. Phys., 22, 14377–14399, https://doi.org/10.5194/acp-22-14377-2022, https://doi.org/10.5194/acp-22-14377-2022, 2022
Short summary
Short summary
Ammonium adduct chemical ionization is used to examine the atmospheric abundances of oxygenated volatile organic compounds associated with emissions from volatile chemical products, which are now key contributors of reactive precursors to ozone and secondary organic aerosols in urban areas. The application of this valuable measurement approach in densely populated New York City enables the evaluation of emissions inventories and thus the role these oxygenated compounds play in urban air quality.
Vanessa Selimovic, Damien Ketcherside, Sreelekha Chaliyakunnel, Catherine Wielgasz, Wade Permar, Hélène Angot, Dylan B. Millet, Alan Fried, Detlev Helmig, and Lu Hu
Atmos. Chem. Phys., 22, 14037–14058, https://doi.org/10.5194/acp-22-14037-2022, https://doi.org/10.5194/acp-22-14037-2022, 2022
Short summary
Short summary
Arctic warming has led to an increase in plants that emit gases in response to stress, but how these gases affect regional chemistry is largely unknown due to lack of observational data. Here we present the most comprehensive gas-phase measurements for this area to date and compare them to predictions from a global transport model. We report 78 gas-phase species and investigate their importance to atmospheric chemistry in the area, with broader implications for similar plant types.
Rujing Yin, Xiaoxiao Li, Chao Yan, Runlong Cai, Ying Zhou, Juha Kangasluoma, Nina Sarnela, Janne Lampilahti, Tuukka Petäjä, Veli-Matti Kerminen, Federico Bianchi, Markku Kulmala, and Jingkun Jiang
EGUsphere, https://doi.org/10.5194/egusphere-2022-1108, https://doi.org/10.5194/egusphere-2022-1108, 2022
Short summary
Short summary
The negative cluster ions with specific compositions are measured and quantified through the in-situ measurement of an atmospheric pressure interface high-resolution time-of-flight mass spectrometer and a neutral cluster and air ion spectrometer in urban Beijing. The governing factors of atmospheric negative cluster ion concentration and composition at polluted urban sites are revealed and the fate of two representative ions in the urban atmosphere is characterized.
Louise Bøge Frederickson, Ruta Sidaraviciute, Johan Albrecht Schmidt, Ole Hertel, and Matthew Stanley Johnson
Atmos. Chem. Phys., 22, 13949–13965, https://doi.org/10.5194/acp-22-13949-2022, https://doi.org/10.5194/acp-22-13949-2022, 2022
Short summary
Short summary
Low-cost sensors see additional pollution that is not seen with traditional regional air quality monitoring stations. This additional local pollution is sufficient to cause exceedance of the World Health Organization exposure thresholds. Analysis shows that a significant amount of the NO2 pollution we observe is local, mainly due to road traffic. This article demonstrates how networks of nodes containing low-cost pollution sensors can powerfully extend existing monitoring programmes.
David D. Parrish, Richard G. Derwent, Ian C. Faloona, and Charles A. Mims
Atmos. Chem. Phys., 22, 13423–13430, https://doi.org/10.5194/acp-22-13423-2022, https://doi.org/10.5194/acp-22-13423-2022, 2022
Short summary
Short summary
Accounting for the continuing long-term decrease of pollution ozone and the large 2020 Arctic stratospheric ozone depletion event improves estimates of background ozone changes caused by COVID-19-related emission reductions; they are smaller than reported earlier. Cooperative, international emission control efforts aimed at maximizing the ongoing decrease in hemisphere-wide background ozone may be the most effective approach to improving ozone pollution in northern midlatitude countries.
Wendell W. Walters, Madeline Karod, Emma Willcocks, Bok H. Baek, Danielle E. Blum, and Meredith G. Hastings
Atmos. Chem. Phys., 22, 13431–13448, https://doi.org/10.5194/acp-22-13431-2022, https://doi.org/10.5194/acp-22-13431-2022, 2022
Short summary
Short summary
Atmospheric ammonia and its products are a significant source of urban haze and nitrogen deposition. We have investigated the seasonal source contributions to a mid-sized city in the northeastern US megalopolis utilizing geospatial statistical analysis and novel isotopic constraints, which indicate that vehicle emissions were significant components of the urban-reduced nitrogen budget. Reducing vehicle ammonia emissions should be considered to improve ecosystems and human health.
Zhaofeng Tan, Hendrik Fuchs, Andreas Hofzumahaus, William J. Bloss, Birger Bohn, Changmin Cho, Thorsten Hohaus, Frank Holland, Chandrakiran Lakshmisha, Lu Liu, Paul S. Monks, Anna Novelli, Doreen Niether, Franz Rohrer, Ralf Tillmann, Thalassa S. E. Valkenburg, Vaishali Vardhan, Astrid Kiendler-Scharr, Andreas Wahner, and Roberto Sommariva
Atmos. Chem. Phys., 22, 13137–13152, https://doi.org/10.5194/acp-22-13137-2022, https://doi.org/10.5194/acp-22-13137-2022, 2022
Short summary
Short summary
During the 2019 JULIAC campaign, ClNO2 was measured at a rural site in Germany in different seasons. The highest ClNO2 level was 1.6 ppbv in September. ClNO2 production was more sensitive to the availability of NO2 than O3. The average ClNO2 production efficiency was up to 18 % in February and September and down to 3 % in December. These numbers are at the high end of the values reported in the literature, indicating the importance of ClNO2 chemistry in rural environments in midwestern Europe.
Xinping Yang, Keding Lu, Xuefei Ma, Yue Gao, Zhaofeng Tan, Haichao Wang, Xiaorui Chen, Xin Li, Xiaofeng Huang, Lingyan He, Mengxue Tang, Bo Zhu, Shiyi Chen, Huabin Dong, Limin Zeng, and Yuanhang Zhang
Atmos. Chem. Phys., 22, 12525–12542, https://doi.org/10.5194/acp-22-12525-2022, https://doi.org/10.5194/acp-22-12525-2022, 2022
Short summary
Short summary
We present the OH and HO2 radical observations at the Shenzhen site (Pearl River Delta, China) in the autumn of 2018. The diurnal maxima were 4.5 × 106 cm−3 for OH and 4.2 × 108 cm−3 for HO2 (including an estimated interference of 23 %–28 % from RO2 radicals during the daytime). The OH underestimation was identified again, and it was attributable to the missing OH sources. HO2 heterogeneous uptake, ROx sources and sinks, and the atmospheric oxidation capacity were evaluated as well.
Katherine L. Hayden, Shao-Meng Li, John Liggio, Michael J. Wheeler, Jeremy J. B. Wentzell, Amy Leithead, Peter Brickell, Richard L. Mittermeier, Zachary Oldham, Cristian M. Mihele, Ralf M. Staebler, Samar G. Moussa, Andrea Darlington, Mengistu Wolde, Daniel Thompson, Jack Chen, Debora Griffin, Ellen Eckert, Jenna C. Ditto, Megan He, and Drew R. Gentner
Atmos. Chem. Phys., 22, 12493–12523, https://doi.org/10.5194/acp-22-12493-2022, https://doi.org/10.5194/acp-22-12493-2022, 2022
Short summary
Short summary
In this study, airborne measurements provided the most detailed characterization, to date, of boreal forest wildfire emissions. Measurements showed a large diversity of air pollutants expanding the volatility range typically reported. A large portion of organic species was unidentified, likely comprised of complex organic compounds. Aircraft-derived emissions improve wildfire chemical speciation and can support reliable model predictions of pollution from boreal forest wildfires.
Albane Barbero, Roberto Grilli, Markus M. Frey, Camille Blouzon, Detlev Helmig, Nicolas Caillon, and Joël Savarino
Atmos. Chem. Phys., 22, 12025–12054, https://doi.org/10.5194/acp-22-12025-2022, https://doi.org/10.5194/acp-22-12025-2022, 2022
Short summary
Short summary
The high reactivity of the summer Antarctic boundary layer results in part from the emissions of nitrogen oxides produced during photo-denitrification of the snowpack, but its underlying mechanisms are not yet fully understood. The results of this study suggest that more NO2 is produced from the snowpack early in the photolytic season, possibly due to stronger UV irradiance caused by a smaller solar zenith angle near the solstice.
Lulu Cui, Di Wu, Shuxiao Wang, Qingcheng Xu, Ruolan Hu, and Jiming Hao
Atmos. Chem. Phys., 22, 11931–11944, https://doi.org/10.5194/acp-22-11931-2022, https://doi.org/10.5194/acp-22-11931-2022, 2022
Short summary
Short summary
A 1-year campaign was conducted to characterize VOCs at a Beijing urban site during different episodes. VOCs from fuel evaporation and diesel exhaust, particularly toluene, xylenes, trans-2-butene, acrolein, methyl methacrylate, vinyl acetate, 1-butene, and 1-hexene, were the main contributors. VOCs from diesel exhaust as well as coal and biomass combustion were found to be the dominant contributors for SOAFP, particularly the VOC species toluene, 1-hexene, xylenes, ethylbenzene, and styrene.
Marcel Zauner-Wieczorek, Martin Heinritzi, Manuel Granzin, Timo Keber, Andreas Kürten, Katharina Kaiser, Johannes Schneider, and Joachim Curtius
Atmos. Chem. Phys., 22, 11781–11794, https://doi.org/10.5194/acp-22-11781-2022, https://doi.org/10.5194/acp-22-11781-2022, 2022
Short summary
Short summary
We present measurements of ambient ions in the free troposphere and lower stratosphere over Europe in spring 2020. We observed nitrate and hydrogen sulfate, amongst others. From their ratio, the number concentrations of gaseous sulfuric acid were inferred. Nitrate increased towards the stratosphere, whilst sulfuric acid was slightly decreased there. The average values for sulfuric acid were 1.9 to 7.8 × 105 cm-3. Protonated pyridine was identified in an altitude range of 4.6 to 8.5 km.
Alena Dekhtyareva, Mark Hermanson, Anna Nikulina, Ove Hermansen, Tove Svendby, Kim Holmén, and Rune Grand Graversen
Atmos. Chem. Phys., 22, 11631–11656, https://doi.org/10.5194/acp-22-11631-2022, https://doi.org/10.5194/acp-22-11631-2022, 2022
Short summary
Short summary
Despite decades of industrial activity in Svalbard, there is no continuous air pollution monitoring in the region’s settlements except Ny-Ålesund. The NOx and O3 observations from the three-station network have been compared for the first time in this study. It has been shown how the large-scale weather regimes control the synoptic meteorological conditions and determine the atmospheric long-range transport pathways and efficiency of local air pollution dispersion.
Asher P. Mouat, Clare Paton-Walsh, Jack B. Simmons, Jhonathan Ramirez-Gamboa, David W. T. Griffith, and Jennifer Kaiser
Atmos. Chem. Phys., 22, 11033–11047, https://doi.org/10.5194/acp-22-11033-2022, https://doi.org/10.5194/acp-22-11033-2022, 2022
Short summary
Short summary
We examine emissions of volatile organic compounds from 2020 wildfires in forested regions of Australia (AU). We find that biomass burning in temperate regions of the US and AU emit similar species in similar proportion, both in natural and lab settings. This suggests studies of wildfires in one region may be used to help improve air quality models in other parts of the world. We observe time series of ozone and nitrogen dioxide. Last, we look at which compounds contribute most to OH reactivity.
Shang Liu, Barbara Barletta, Rebecca S. Hornbrook, Alan Fried, Jeff Peischl, Simone Meinardi, Matthew Coggon, Aaron Lamplugh, Jessica B. Gilman, Georgios I. Gkatzelis, Carsten Warneke, Eric C. Apel, Alan J. Hills, Ilann Bourgeois, James Walega, Petter Weibring, Dirk Richter, Toshihiro Kuwayama, Michael FitzGibbon, and Donald Blake
Atmos. Chem. Phys., 22, 10937–10954, https://doi.org/10.5194/acp-22-10937-2022, https://doi.org/10.5194/acp-22-10937-2022, 2022
Short summary
Short summary
California’s ozone persistently exceeds the air quality standards. We studied the spatial distribution of volatile organic compounds (VOCs) that produce ozone over the most polluted regions in California using aircraft measurements. We find that the oxygenated VOCs have the highest ozone formation potential. Spatially, biogenic VOCs are important during high ozone episodes in the South Coast Air Basin, while dairy emissions may be critical for ozone production in San Joaquin Valley.
Simone M. Pieber, Béla Tuzson, Stephan Henne, Ute Karstens, Christoph Gerbig, Frank-Thomas Koch, Dominik Brunner, Martin Steinbacher, and Lukas Emmenegger
Atmos. Chem. Phys., 22, 10721–10749, https://doi.org/10.5194/acp-22-10721-2022, https://doi.org/10.5194/acp-22-10721-2022, 2022
Short summary
Short summary
Understanding regional greenhouse gas emissions into the atmosphere is a prerequisite to mitigate climate change. In this study, we investigated the regional contributions of carbon dioxide (CO2) at the location of the high Alpine observatory Jungfraujoch (JFJ, Switzerland, 3580 m a.s.l.). To this purpose, we combined receptor-oriented atmospheric transport simulations for CO2 concentration in the period 2009–2017 with stable carbon isotope (δ13C–CO2) information.
Xiao-Bing Li, Bin Yuan, Sihang Wang, Chunlin Wang, Jing Lan, Zhijie Liu, Yongxin Song, Xianjun He, Yibo Huangfu, Chenglei Pei, Peng Cheng, Suxia Yang, Jipeng Qi, Caihong Wu, Shan Huang, Yingchang You, Ming Chang, Huadan Zheng, Wenda Yang, Xuemei Wang, and Min Shao
Atmos. Chem. Phys., 22, 10567–10587, https://doi.org/10.5194/acp-22-10567-2022, https://doi.org/10.5194/acp-22-10567-2022, 2022
Short summary
Short summary
High-time-resolution measurements of volatile organic compounds (VOCs) were made using an online mass spectrometer at a 600 m tall tower in urban region. Compositions, temporal variations, and sources of VOCs were quantitatively investigated in this study. We find that VOC measurements in urban regions aloft could better characterize source characteristics of anthropogenic emissions. Our results could provide important implications in making future strategies for control of VOCs.
Robert J. Yokelson, Bambang H. Saharjo, Chelsea E. Stockwell, Erianto I. Putra, Thilina Jayarathne, Acep Akbar, Israr Albar, Donald R. Blake, Laura L. B. Graham, Agus Kurniawan, Simone Meinardi, Diah Ningrum, Ati D. Nurhayati, Asmadi Saad, Niken Sakuntaladewi, Eko Setianto, Isobel J. Simpson, Elizabeth A. Stone, Sigit Sutikno, Andri Thomas, Kevin C. Ryan, and Mark A. Cochrane
Atmos. Chem. Phys., 22, 10173–10194, https://doi.org/10.5194/acp-22-10173-2022, https://doi.org/10.5194/acp-22-10173-2022, 2022
Short summary
Short summary
Fire plus non-fire GHG emissions associated with draining peatlands are the largest per area of any land use change considered by the IPCC. To characterize average and variability for tropical peat fire emissions, highly mobile smoke sampling teams were deployed across four Indonesian provinces to explore an extended interannual, climatic, and spatial range. Large adjustments to IPCC-recommended emissions are suggested. Lab data bolster an extensive emissions database for tropical peat fires.
Deanna C. Myers, Saewung Kim, Steven Sjostedt, Alex B. Guenther, Roger Seco, Oscar Vega Bustillos, Julio Tota, Rodrigo A. F. Souza, and James N. Smith
Atmos. Chem. Phys., 22, 10061–10076, https://doi.org/10.5194/acp-22-10061-2022, https://doi.org/10.5194/acp-22-10061-2022, 2022
Short summary
Short summary
We present the first measurements of gas-phase sulfuric acid from the Amazon basin and evaluate the efficacy of existing sulfuric acid parameterizations in this understudied region. Sulfuric acid is produced during the daytime and nighttime, though current proxies underestimate nighttime production. These results illustrate the need for better parameterizations of sulfuric acid and its precursors that are informed by measurements across a broad range of locations.
Yishuo Guo, Chao Yan, Yuliang Liu, Xiaohui Qiao, Feixue Zheng, Ying Zhang, Ying Zhou, Chang Li, Xiaolong Fan, Zhuohui Lin, Zemin Feng, Yusheng Zhang, Penggang Zheng, Linhui Tian, Wei Nie, Zhe Wang, Dandan Huang, Kaspar R. Daellenbach, Lei Yao, Lubna Dada, Federico Bianchi, Jingkun Jiang, Yongchun Liu, Veli-Matti Kerminen, and Markku Kulmala
Atmos. Chem. Phys., 22, 10077–10097, https://doi.org/10.5194/acp-22-10077-2022, https://doi.org/10.5194/acp-22-10077-2022, 2022
Short summary
Short summary
Gaseous oxygenated organic molecules (OOMs) are able to form atmospheric aerosols, which will impact on human health and climate change. Here, we find that OOMs in urban Beijing are dominated by anthropogenic sources, i.e. aromatic (29 %–41 %) and aliphatic (26 %–41 %) OOMs. They are also the main contributors to the condensational growth of secondary organic aerosols (SOAs). Therefore, the restriction on anthropogenic VOCs is crucial for the reduction of SOAs and haze formation.
Sihang Wang, Bin Yuan, Caihong Wu, Chaomin Wang, Tiange Li, Xianjun He, Yibo Huangfu, Jipeng Qi, Xiao-Bing Li, Qing'e Sha, Manni Zhu, Shengrong Lou, Hongli Wang, Thomas Karl, Martin Graus, Zibing Yuan, and Min Shao
Atmos. Chem. Phys., 22, 9703–9720, https://doi.org/10.5194/acp-22-9703-2022, https://doi.org/10.5194/acp-22-9703-2022, 2022
Short summary
Short summary
Volatile organic compound (VOC) emissions from vehicles are measured using online mass spectrometers. Differences between gasoline and diesel vehicles are observed with higher emission factors of most oxygenated VOCs (OVOCs) and heavier aromatics from diesel vehicles. A higher aromatics / toluene ratio could provide good indicators to distinguish emissions from both vehicle types. We show that OVOCs account for significant contributions to VOC emissions from vehicles, especially diesel vehicles.
Keming Pan and Ian C. Faloona
Atmos. Chem. Phys., 22, 9681–9702, https://doi.org/10.5194/acp-22-9681-2022, https://doi.org/10.5194/acp-22-9681-2022, 2022
Short summary
Short summary
This work represents a unique analysis of 10 existing air quality network sites and meteorological sites, two AmeriFlux sites, and a radio acoustic sounding system in the Central Valley of California during five consecutive fire seasons, June through September, from 2016 to 2020. We find that the ozone production rate increases by ~ 50 % during wildfire influenced periods. Wildfire smoke also decreases the heat flux by 30 % and results in 12 % lower mixed-layer height.
Zaneta T. Hamryszczak, Andrea Pozzer, Florian Obersteiner, Birger Bohn, Benedikt Steil, Jos Lelieveld, and Horst Fischer
Atmos. Chem. Phys., 22, 9483–9497, https://doi.org/10.5194/acp-22-9483-2022, https://doi.org/10.5194/acp-22-9483-2022, 2022
Short summary
Short summary
Hydrogen peroxide plays a pivotal role in the chemistry of the atmosphere. Together with organic hydroperoxides, it forms a reservoir for peroxy radicals, which are known to be the key contributors to the self-cleaning processes of the atmosphere. Hydroperoxides were measured over Europe during the BLUESKY campaign in May–June 2020. The paper gives an overview of the distribution of the species in the troposphere and investigates the impact of wet scavenging and deposition on the budget of H2O2.
Cited articles
Akagi, S. K., Yokelson, R. J., Wiedinmyer, C., Alvarado, M. J., Reid, J. S., Karl, T., Crounse, J. D., and Wennberg, P. O.: Emission factors for open and domestic biomass burning for use in atmospheric models, Atmos. Chem. Phys., 11, 4039–4072, https://doi.org/10.5194/acp-11-4039-2011, 2011.
Akagi, S. K., Yokelson, R. J., Burling, I. R., Meinardi, S., Simpson, I., Blake, D. R., McMeeking, G. R., Sullivan, A., Lee, T., Kreidenweis, S., Urbanski, S., Reardon, J., Griffith, D. W. T., Johnson, T. J., and Weise, D. R.: Measurements of reactive trace gases and variable O3 formation rates in some South Carolina biomass burning plumes, Atmos. Chem. Phys., 13, 1141–1165, https://doi.org/10.5194/acp-13-1141-2013, 2013.
Akagi, S. K., Burling, I. R., Mendoza, A., Johnson, T. J., Cameron, M., Griffith, D. W. T., Paton-Walsh, C., Weise, D. R., Reardon, J., and Yokelson, R. J.: Field measurements of trace gases emitted by prescribed fires in southeastern US pine forests using an open-path FTIR system, Atmos. Chem. Phys., 14, 199–215, https://doi.org/10.5194/acp-14-199-2014, 2014.
Albini, F. A.: Estimating wildfire behavior and effects, USDA Forest Service
General Technical Report, INT-30, 1976.
Alves, C. A., Gonçalves, C., Pio, C. A., Mirante, F., Caseiro, A.,
Tarelho, L., Freitas, M. C., and Viegas, D. X.: Smoke emissions from biomass
burning in a Mediterranean shrubland, Atmos. Environ., 44, 3024–3033, 2010.
Amini, E., Safdari, M.-S., DeYoung, J. T., Weise, D. R., and Fletcher, T.
H.: Characterization of pyrolysis products from slow pyrolysis of live and
dead vegetation native to the southern United States, Fuel, 235, 1475–1491,
https://doi.org/10.1016/j.fuel.2018.08.112, 2019a.
Amini, E., Safdari, M.-S., Weise, D. R., and Fletcher, T. H.: Pyrolysis
Kinetics of Live and Dead Wildland Vegetation from the Southern United
States, J. Anal. Appl. Pyrol., https://doi.org/10.1016/j.jaap.2019.05.002, 2019b.
Andreae, M. O.: Biomass burning: Its history, use, and distribution and its
impact on environmental quality and global climate, in: Global Biomass
Burning: Atmospheric, Climatic, and Biospheric Implications, edited by:
Levine, J. S., MIT Press, Cambridge, Mass, 3–21, 1991.
Andreae, M. O. and Merlet, P.: Emission of trace gases and aerosols from
biomass burning, Global Biogeochem. Cy., 15, 955–966, 2001.
Andreae, M. O., Browell, E. V., Garstang, M., Gregory, G. L., Harriss, R.
C., Hill, G. F., Jacob, D. J., Pereira, M. C., Sachse, G. W., Setzer, A. W.,
Silva Dias, P. L., Talbot, R. W., Torres, A. L., and Wofsy, S. C.:
Biomass-burning emissions and associated haze layers over Amazonia, J.
Geophys. Res.-Atmos., 93, 1509–1527, 1988.
Andreae, M. O., Anderson, B. E., Blake, D. R., Bradshaw, J. D., Collins, J.
E., Gregory, G. L., Sachse, G. W., and Shipham, M. C.: Influence of plumes
from biomass burning on atmospheric chemistry over the equatorial and
tropical South Atlantic during CITE 3, J. Geophys. Res.-Atmos., 99,
12793–12808, 1994.
Azeez, A. M., Meier, D., and Odermatt, J.: Temperature dependence of fast
pyrolysis volatile products from European and African biomasses, J. Anal.
Appl. Pyrol., 90, 81–92, 2011.
Bai, X., Johnston, P., Sadula, S., and Brown, R. C.: Role of levoglucosan
physiochemistry in cellulose pyrolysis, J. Anal. Appl. Pyrol., 99, 58–65,
2013.
Boschan, R., Merrow, R. T., and van Dolah, R. W.: The chemistry of nitrate
esters, Chem. Rev., 55, 485–510, 1955.
Burling, I. R., Yokelson, R. J., Griffith, D. W. T., Johnson, T. J., Veres, P., Roberts, J. M., Warneke, C., Urbanski, S. P., Reardon, J., Weise, D. R., Hao, W. M., and de Gouw, J.: Laboratory measurements of trace gas emissions from biomass burning of fuel types from the southeastern and southwestern United States, Atmos. Chem. Phys., 10, 11115–11130, https://doi.org/10.5194/acp-10-11115-2010, 2010.
Burling, I. R., Yokelson, R. J., Akagi, S. K., Urbanski, S. P., Wold, C. E., Griffith, D. W. T., Johnson, T. J., Reardon, J., and Weise, D. R.: Airborne and ground-based measurements of the trace gases and particles emitted by prescribed fires in the United States, Atmos. Chem. Phys., 11, 12197–12216, https://doi.org/10.5194/acp-11-12197-2011, 2011.
Cary, A.: Some relations of fire to longleaf pine, J. For., 30, 594–601,
1932.
Chi, C., Horn, D., Reznik, R., Zanders, D., Opferkuch, R., Nyers, J.,
Pierovich, J., Lavdas, L., Mcmahon, C., and Nelson, R.: Source assessment:
prescribed burning, state of the art, US Environmental Protection Agency,
EPA (US) Report EPA-600/2-79-019h, 1979.
Christian, T. J., Kleiss, B., Yokelson, R. J., Holzinger, R., Crutzen, P.
J., Hao, W. M., Saharjo, B. H., and Ward, D. E.: Comprehensive laboratory
measurements of biomass-burning emissions: 1. Emissions from Indonesian,
African, and other fuels, J. Geophys. Res.-Atmos., 108, 4719,
https://doi.org/10.1029/2003JD003704, 2003.
Christian, T. J., Kleiss, B., Yokelson, R. J., Holzinger, R., Crutzen, P.
J., Hao, W. M., Shirai, T., and Blake, D. R.: Comprehensive laboratory
measurements of biomass-burning emissions: 2. First intercomparison of
open-path FTIR, PTR-MS, and GC-MS/FID/ECD, J. Geophys. Res.-Atmos., 109, D02311, https://doi.org/10.1029/2003JD003874,
2004.
Clark, M. M., Fletcher, T. H., and Linn, R. R.: A sub-grid,
mixture–fraction-based thermodynamic equilibrium model for gas phase
combustion in FIRETEC: development and results, Int. J.
Wildland Fire, 19, 202–212, 2010.
Coggon, M. M., Veres, P. R., Yuan, B., Koss, A., Warneke, C., Gilman, J. B.,
Lerner, B. M., Peischl, J., Aikin, K. C., Stockwell, C. E., Hatch, L. E.,
Ryerson, T. B., Roberts, J. M., Yokelson, R. J., and de Gouw, J. A.:
Emissions of nitrogen-containing organic compounds from the burning of
herbaceous and arboraceous biomass: Fuel composition dependence and the
variability of commonly used nitrile tracers, Geophys. Res. Lett., 43,
9903–9912, 2016.
Collard, F.-X. and Blin, J.: A review on pyrolysis of biomass constituents:
Mechanisms and composition of the products obtained from the conversion of
cellulose, hemicelluloses and lignin, Renew. Sustain. Energy Rev., 38,
594–608, 2014.
Crutzen, P. J., Heidt, L. E., Krasnec, J. P., Pollock, W. H., and Seiler,
W.: Biomass burning as a source of atmospheric gases CO, H2, N2O, NO, CH3Cl
and COS, Nature, 282, 253–256, https://doi.org/10.1038/282253a0, 1979.
Crutzen, P. J. and Andreae, M. O.: Biomass burning in the tropics: Impact
on atmospheric chemistry and biogeochemical cycles, Science, 250, 1669–1678,
1990.
DeGroot, W. F., Pan, W.-P., Rahman, M. D., and Richards, G. N.: First
chemical events in pyrolysis of wood, J. Anal. Appl.
Pyrol., 13, 221–231, 1988.
Di Blasi, C.: Modeling and simulation of combustion processes of charring
and non-charring solid fuels, Prog. Energy Combust. Sci., 19, 71–104, 1993.
Di Blasi, C.: Modeling chemical and physical processes of wood and biomass
pyrolysis, Prog. Energy Combust. Sci., 34, 47–90, 2008.
Dlugokencky, E., and Tans, P.: NOAA/ESRL, available at:
https://www.esrl.noaa.gov/gmd/ccgg/trends/ (last access: 22 July 2019), 2012.
Fagernäs, L., Kuoppala, E., and Simell, P.: Polycyclic
aromatic hydrocarbons in birch wood slow pyrolysis products, Energy Fuels,
26, 6960–6970, 2012.
Fairburn, J. A., Behie, L. A., and Svrcek, W. Y.: Ultrapyrolysis of
n-hexadecane in a novel micro-reactor, Fuel, 69, 1537–1545, 1990.
Ferguson, S. C., Dahale, A., Shotorban, B., Mahalingam, S., and Weise, D.
R.: The role of moisture on combustion of pyrolysis gases in wildland fires,
Combust. Sci. Technol., 185, 435–453, 2013.
Fernandes, P. M. and Botelho, H. S.: A review of prescribed burning
effectiveness in fire hazard reduction, Int. J. Wildland Fire, 12, 117–128,
2003.
Gilman, J. B., Lerner, B. M., Kuster, W. C., Goldan, P. D., Warneke, C., Veres, P. R., Roberts, J. M., de Gouw, J. A., Burling, I. R., and Yokelson, R. J.: Biomass burning emissions and potential air quality impacts of volatile organic compounds and other trace gases from fuels common in the US, Atmos. Chem. Phys., 15, 13915–13938, https://doi.org/10.5194/acp-15-13915-2015, 2015.
Goode, J. G., Yokelson, R. J., Susott, R. A., and Ward, D. E.: Trace gas
emissions from laboratory biomass fires measured by open-path Fourier
transform infrared spectroscopy: Fires in grass and surface fuels, J.
Geophys. Res.-Atmos., 104, 21237–21245, 1999.
Goode, J. G., Yokelson, R. J., Ward, D. E., Susott, R. A., Babbitt, R. E.,
Davies, M. A., and Hao, W. M.: Measurements of excess O3, CO2, CO,
CH4, C2H4, C2H2, HCN, NO, NH3, HCOOH,
CH3COOH, HCHO, and CH3OH in 1997 Alaskan biomass burning plumes by
airborne Fourier transform infrared spectroscopy (AFTIR), J. Geophys. Res.-Atmos., 105, 22147–22166, 2000.
Gordon, I. E., Rothman, L. S., Hill, C., Kochanov, R. V., Tan, Y., Bernath,
P. F., Birk, M., Boudon, V., Campargue, A., Chance, K. V., Drouin, B. J.,
Flaud, J.-M., Gamache, R. R., Hodges, J. T., Jacquemart, D., Perevalov, V.
I., Perrin, A., Shine, K. P., Smith, M.-A. H., Tennyson, J., Toon, G. C.,
Tran, H., Tyuterev, V. G., Barbe, A., Császár, A. G., Devi, V. M.,
Furtenbacher, T., Harrison, J. J., Hartmann, J.-M., Jolly, A., Johnson, T.
J., Karman, T., Kleiner, I., Kyuberis, A. A., Loos, J., Lyulin, O. M.,
Massie, S. T., Mikhailenko, S. N., Moazzen-Ahmadi, N., Müller, H. S. P.,
Naumenko, O. V., Nikitin, A. V., Polyansky, O. L., Rey, M., Rotger, M.,
Sharpe, S. W., Sung, K., Starikova, D., Tashkun, S. A., Vander Auwera, J.,
Wagner, G., Wilzewski, J., Wcisło, P., Yu, S., and Zak, E.
J.: The HITRAN2016 molecular spectroscopic database, J. Quant. Spectrosc.
Ra., 203, 3–69, 2017.
Griffith, D. W. T.: MALT5 User guide Version 5.5.9, 2016.
Griffiths, J. F., Gilligan, M. F., and Gray, P.: Pyrolysis of isopropyl
nitrate. I. Decomposition at low temperatures and pressures, Combust. Flame,
24, 11–19, 1975.
Guérette, E.-A., Paton-Walsh, C., Desservettaz, M., Smith, T. E. L., Volkova, L., Weston, C. J., and Meyer, C. P.: Emissions of trace gases from Australian temperate forest fires: emission factors and dependence on modified combustion efficiency, Atmos. Chem. Phys., 18, 3717–3735, https://doi.org/10.5194/acp-18-3717-2018, 2018.
Haidar, N. F., Patterson, J. M., Moors, M., and Smith Jr, W. T.: Effects of
structure on pyrolysis gases from amino acids, J. Agric. Food Chem., 29,
163–165, 1981.
Hansson, K.-M., Samuelsson, J., Tullin, C., and Åmand, L.-E.: Formation
of HNCO, HCN, and NH3 from the pyrolysis of bark and
nitrogen-containing model compounds, Combust. Flame, 137, 265–277, 2004.
Hatch, L. E., Yokelson, R. J., Stockwell, C. E., Veres, P. R., Simpson, I. J., Blake, D. R., Orlando, J. J., and Barsanti, K. C.: Multi-instrument comparison and compilation of non-methane organic gas emissions from biomass burning and implications for smoke-derived secondary organic aerosol precursors, Atmos. Chem. Phys., 17, 1471–1489, https://doi.org/10.5194/acp-17-1471-2017, 2017.
Hurst, D. F., Griffith, D. W. T., Carras, J. N., Williams, D. J., and
Fraser, P. J.: Measurements of trace gases emitted by Australian savanna
fires during the 1990 dry season, J. Atmos. Chem., 18, 33–56, 1994a.
Hurst, D. F., Griffith, D. W. T., and Cook, G. D.: Trace gas emissions from
biomass burning in tropical Australian savannas, J. Geophys. Res.-Atmos.,
99, 16441–16456, 1994b.
Johnson, T. J., Masiello, T., and Sharpe, S. W.: The quantitative infrared and NIR spectrum of CH2I2 vapor: vibrational assignments and potential for atmospheric monitoring, Atmos. Chem. Phys., 6, 2581–2591, https://doi.org/10.5194/acp-6-2581-2006, 2006.
Johnson, T. J., Sams, R. L., Burton, S. D., and Blake, T. A.: Absolute
integrated intensities of vapor-phase hydrogen peroxide (H2O2) in
the mid-infrared at atmospheric pressure, Anal. Bioanal. Chem., 395,
377–386, 2009.
Johnson, T. J., Profeta, L. T. M., Sams, R. L., Griffith, D. W. T., and
Yokelson, R. L.: An infrared spectral database for detection of gases
emitted by biomass burning, Vib. Spectrosc., 53, 97–102, 2010.
Johnson, T. J., Sams, R. L., Profeta, L. T., Akagi, S. K., Burling, I. R.,
Yokelson, R. J., and Williams, S. D.: Quantitative IR spectrum and
vibrational assignments for glycolaldehyde vapor: glycolaldehyde
measurements in biomass burning plumes, J. Phys. Chem. A, 117, 4096–4107,
2013.
Johnson, W. R. and Kan, J. C.: Mechanisms of hydrogen cyanide formation
from the pyrolysis of amino acids and related compounds, J. Org. Chem., 36,
189–192, 1971.
Karl, T. G., Christian, T. J., Yokelson, R. J., Artaxo, P., Hao, W. M., and Guenther, A.: The Tropical Forest and Fire Emissions Experiment: method evaluation of volatile organic compound emissions measured by PTR-MS, FTIR, and GC from tropical biomass burning, Atmos. Chem. Phys., 7, 5883–5897, https://doi.org/10.5194/acp-7-5883-2007, 2007.
Kibet, J., Khachatryan, L., and Dellinger, B.: Molecular products and
radicals from pyrolysis of lignin, Environ. Sci. Technol., 46, 12994–13001,
2012.
Koss, A. R., Sekimoto, K., Gilman, J. B., Selimovic, V., Coggon, M. M., Zarzana, K. J., Yuan, B., Lerner, B. M., Brown, S. S., Jimenez, J. L., Krechmer, J., Roberts, J. M., Warneke, C., Yokelson, R. J., and de Gouw, J.: Non-methane organic gas emissions from biomass burning: identification, quantification, and emission factors from PTR-ToF during the FIREX 2016 laboratory experiment, Atmos. Chem. Phys., 18, 3299–3319, https://doi.org/10.5194/acp-18-3299-2018, 2018.
Ledesma, E. B., Marsh, N. D., Sandrowitz, A. K., and Wornat, M. J.: Global
kinetic rate parameters for the formation of polycyclic aromatic
hydrocarbons from the pyrolyis of catechol, a model compound representative
of solid fuel moieties, Energy Fuels, 16, 1331–1336, 2002.
Lindenmaier, R., Tipton, N., Sams, R. L., Brauer, C. S., Blake, T. A.,
Williams, S. D., and Johnson, T. J.: Assignment of the Fundamental Modes of
Hydroxyacetone Using Gas-Phase Infrared, Far-Infrared, Raman, and ab Initio
Methods: Band Strengths for Atmospheric Measurements, J. Phys. Chem. A, 120,
5993–6003, 2016.
Lindesay, J. A., Andreae, M. O., Goldammer, J. G., Harris, G., Annegarn, H.
J., Garstang, M., Scholes, R. J., and Van Wilgen, B. W.: International
geosphere-biosphere programme/international global atmospheric chemistry
SAFARI-92 field experiment: Background and overview, J. Geophys. Res.-Atmos., 101, 23521–23530, 1996.
Liu, X., Zhang, Y., Huey, L. G., Yokelson, R. J., Wang, Y., Jimenez, J. L.,
Campuzano-Jost, P., Beyersdorf, A. J., Blake, D. R., Choi, Y., St. Clair, H.
M., Crounse, J. D., Day, D. A., Diskin, G. S., Fried, A., Hall, S. R.,
Hanisco, T. F., King, L. E., Meinardi, S., Mikoviny, T., Palm, B. B.,
Peischl, J., Perring, A. E., Pollack, I. B., Ryerson, T. B., Sachse, G.,
Schwarz, J. P., Simpson, I. J., Tanner, D. J., Thornhill, K. L., Ullmann,
K., Weber, R. J., Wennberg, P. O., Wisthaler, A., Wolfe, G. M., and Ziemba,
L. D.: Agricultural fires in the southeastern US during SEAC4RS: Emissions
of trace gases and particles and evolution of ozone, reactive nitrogen, and
organic aerosol, J. Geophys. Res.-Atmos., 121,
7383–7414, https://doi.org/10.1002/2016JD025040, 2016.
Liu, X., Huey, L. G., Yokelson, R. J., Selimovic, V., Simpson, I. J.,
Müller, M., Jimenez, J. L., Campuzano-Jost, P., Beyersdorf, A. J.,
Blake, D. R., Butterfield, Z., Choi, Y., Crounse, J. D., Day, D. A., Diskin,
G. S., Dubey, M. K., Fortner, E., Hanisco, T. F., Hu, W., King, L. E.,
Kleinman, L., Meinardi, S., Milkoviny, T., Onasch, T. B., Palm, B. B.,
Peischl, J., Pollack, I. B., Ryerson, T. B., Sachse, G. W., Sedlacek, A. J.,
Shilling, J. E., Springston, S., St. Clair, J. M., Tanner, D. J., Teng, A.
P., Wennberg, P. O., Wisthaler, A., and Wolfe, G. M.: Airborne measurements
of western US wildfire emissions: Comparison with prescribed burning and air
quality implications, J. Geophys. Res.-Atmos., 122,
6108–6129, 2017.
Lobert, J. M., Scharffe, D. H., Weimin, H., Kuhlbusch, T. A.,Seuwen, R., Warneck, P., and Crutzen, P. J.: Experimental evaluation of biomass burning emissions: Nitrogen and carbon containing
compounds, in: Global Biomass Burning, Atmospheric,climatic, and biospheric implications,
edited by: Levine, J. S., MIT Press, Cambridge, Mass., 1991.
Lu, Q., Yang, X.-C., Dong, C.-Q., Zhang, Z.-F., Zhang, X.-M., and Zhu,
X.-F.: Influence of pyrolysis temperature and time on the cellulose fast
pyrolysis products: Analytical Py-GC/MS study, J. Anal. Appl. Pyrol., 92,
430–438, 2011.
Mell, W., Maranghides, A., McDermott, R., and Manzello, S. L.: Numerical
simulation and experiments of burning douglas fir trees, Combust.
Flame, 156, 2023–2041, 2009.
Melvin, M. A.: National prescribed fire use survey report, Coalition of
Prescribed Fire Councils Technical Report, 01-12, 2012.
Miller, J. D., Safford, H. D., Crimmins, M., and Thode, A. E.: Quantitative
evidence for increasing forest fire severity in the Sierra Nevada and
southern Cascade Mountains, California and Nevada, USA, Ecosystems, 12,
16–32, 2009.
Neuman, J., Huey, L., Ryerson, T., and Fahey, D.: Study of inlet materials
for sampling atmospheric nitric acid, Environ. Sci. Technol.,
33, 1133–1136, 1999.
Palma, C. F.: Modelling of tar formation and evolution for biomass
gasification: a review, Appl. Energy, 111, 129–141, 2013.
Paton-Walsh, C., Wilson, S. R., Jones, N. B., and Griffith, D. W. T.:
Measurement of methanol emissions from Australian wildfires by ground-based
solar Fourier transform spectroscopy, Geophys. Res. Lett., 35, L08810, https://doi.org/10.1029/2007GL032951, 2008.
Paton-Walsh, C., Deutscher, N. M., Griffith, D. W. T., Forgan, B. W.,
Wilson, S. R., Jones, N. B., and Edwards, D. P.: Trace gas emissions from
savanna fires in northern Australia, J. Geophys. Res.-Atmos., 115, D16314, https://doi.org/10.1029/2009JD013309, 2010.
Porcher, R. D. and Rayner, D. A.: A guide to the wildflowers of South
Carolina, University of South Carolina Press Columbia, South Carolina, 2001.
Prichard, S., Ottmar, R., and Anderson, G.: Consume 3.0 user's guide, USDA
Forest Service, p. 234, 2006.
Reinhardt, E. D., Keane, R. E., and Brown, J. K.: First order fire effects
model: FOFEM 4.0, user's guide, Gen. Tech. Rep. INT-GTR-344. Ogden, UT: US
Department of Agriculture, Forest Service, Intermountain Research Station,
65 p., 344, 1997.
Ren, Q., and Zhao, C.: NOx and N2O precursors from biomass
pyrolysis: Nitrogen transformation from amino acid, Environ. Sci. Technol.,
46, 4236–4240, 2012.
Ren, Q. and Zhao, C.: NOx and N2O precursors from biomass
pyrolysis: role of cellulose, hemicellulose and lignin, Environ. Sci.
Technol., 47, 8955–8961, 2013a.
Ren, Q. and Zhao, C.: NOx and N2O precursors (NH3 and HCN)
from biomass pyrolysis: interaction between amino acid and mineral matter,
Appl. Energy, 112, 170–174, 2013b.
Richter, H. and Howard, J. B.: Formation of polycyclic aromatic
hydrocarbons and their growth to soot – a review of chemical reaction
pathways, Prog. Energy Combust. Sci., 26, 565–608, 2000.
Roberts, J. M., Veres, P., Warneke, C., Neuman, J. A., Washenfelder, R. A., Brown, S. S., Baasandorj, M., Burkholder, J. B., Burling, I. R., Johnson, T. J., Yokelson, R. J., and de Gouw, J.: Measurement of HONO, HNCO, and other inorganic acids by negative-ion proton-transfer chemical-ionization mass spectrometry (NI-PT-CIMS): application to biomass burning emissions, Atmos. Meas. Tech., 3, 981–990, https://doi.org/10.5194/amt-3-981-2010, 2010.
Roscioli, J., Zahniser, M., Nelson, D., Herndon, S., and Kolb, C.: New
Approaches to measuring sticky molecules: improvement of instrumental
response times using active passivation, J. Phys. Chem.
A, 120, 1347–1357, 2015.
Rothermel, R. C.: A mathematical model for predicting fire spread in
wildland fuels, INT-115, 1972.
Safdari, M.-S., Rahmati, M., Amini, E., Howarth, J. E., Berryhill, J. P.,
Dietenberger, M., Weise, D. R., and Fletcher, T. H.: Characterization of
pyrolysis products from fast pyrolysis of live and dead vegetation native to
the Southern United States, Fuel, 229, 151–166, 2018.
Safdari, M.-S., Amini, E., Weise, D. R., and Fletcher, T. H.: Heating rate
and temperature effects on pyrolysis products from live wildland fuels,
Fuel, 242, 295–304, 2019.
Scharko, N. K., Oeck, A. M., Tonkyn, R. G., Baker, S. P., Lincoln, E. N., Chong, J., Corcoran, B. M., Burke, G. M., Weise, D. R., Myers, T. L., Banach, C. A., Griffith, D. W. T., and Johnson, T. J.: Identification of gas-phase pyrolysis products in a prescribed fire: first detections using infrared spectroscopy for naphthalene, methyl nitrite, allene, acrolein and acetaldehyde, Atmos. Meas. Tech., 12, 763–776, https://doi.org/10.5194/amt-12-763-2019, 2019.
Seinfeld, J. H. and Pandis, S. N.: Atmospheric chemistry and physics: from
air pollution to climate change, John Wiley & Sons, Hoboken, 2012.
Sekimoto, K., Koss, A. R., Gilman, J. B., Selimovic, V., Coggon, M. M., Zarzana, K. J., Yuan, B., Lerner, B. M., Brown, S. S., Warneke, C., Yokelson, R. J., Roberts, J. M., and de Gouw, J.: High- and low-temperature pyrolysis profiles describe volatile organic compound emissions from western US wildfire fuels, Atmos. Chem. Phys., 18, 9263–9281, https://doi.org/10.5194/acp-18-9263-2018, 2018.
Selimovic, V., Yokelson, R. J., Warneke, C., Roberts, J. M., de Gouw, J., Reardon, J., and Griffith, D. W. T.: Aerosol optical properties and trace gas emissions by PAX and OP-FTIR for laboratory-simulated western US wildfires during FIREX, Atmos. Chem. Phys., 18, 2929–2948, https://doi.org/10.5194/acp-18-2929-2018, 2018.
Shafizadeh, F., McGinnis, G., and Philpot, C.: Thermal degradation of xylan
and related model compounds, Carbohydr. Res., 25, 23–33, 1972.
Sharpe, S. W., Johnson, T. J., Sams, R. L., Chu, P. M., Rhoderick, G. C.,
and Johnson, P. A.: Gas-phase databases for quantitative infrared
spectroscopy, Appl. Spectrosc., 58, 1452–1461, 2004.
Shen, D., Gu, S., and Bridgwater, A. V.: Study on the pyrolytic behaviour of
xylan-based hemicellulose using TG-FTIR and Py-GC-FTIR, J. Anal. Appl.
Pyrol., 87, 199–206, 2010.
Shen, D., Jin, W., Hu, J., Xiao, R., and Luo, K.: An overview on fast
pyrolysis of the main constituents in lignocellulosic biomass to
valued-added chemicals: Structures, pathways and interactions, Renew.
Sustain. Energy Rev., 51, 761–774, 2015.
Shen, D. K. and Gu, S.: The mechanism for thermal decomposition of
cellulose and its main products, Bioresour. Technol., 100, 6496–6504,
https://doi.org/10.1016/j.biortech.2009.06.095, 2009.
Shotorban, B., Yashwanth, B. L., Mahalingam, S., and Haring, D. J.: An
investigation of pyrolysis and ignition of moist leaf-like fuel subject to
convective heating, Combust. Flame, 190, 25–35, 2018.
Simmie, J. M.: Detailed chemical kinetic models for the combustion of
hydrocarbon fuels, Prog. Energy Combust. Sci., 29, 599–634, 2003.
Simpson, I. J., Akagi, S. K., Barletta, B., Blake, N. J., Choi, Y., Diskin, G. S., Fried, A., Fuelberg, H. E., Meinardi, S., Rowland, F. S., Vay, S. A., Weinheimer, A. J., Wennberg, P. O., Wiebring, P., Wisthaler, A., Yang, M., Yokelson, R. J., and Blake, D. R.: Boreal forest fire emissions in fresh Canadian smoke plumes: C1–C10 volatile organic compounds (VOCs), CO2, CO, NO2, NO, HCN and CH3CN, Atmos. Chem. Phys., 11, 6445–6463, https://doi.org/10.5194/acp-11-6445-2011, 2011.
Stein, Y. S., Antal Jr, M. J., and Jones Jr., M.: A study of the gas-phase
pyrolysis of glycerol, J. Anal. Appl. Pyrol., 4, 283–296, 1983.
Stockwell, C. E., Yokelson, R. J., Kreidenweis, S. M., Robinson, A. L., DeMott, P. J., Sullivan, R. C., Reardon, J., Ryan, K. C., Griffith, D. W. T., and Stevens, L.: Trace gas emissions from combustion of peat, crop residue, domestic biofuels, grasses, and other fuels: configuration and Fourier transform infrared (FTIR) component of the fourth Fire Lab at Missoula Experiment (FLAME-4), Atmos. Chem. Phys., 14, 9727–9754, https://doi.org/10.5194/acp-14-9727-2014, 2014.
Stockwell, C. E., Jayarathne, T., Cochrane, M. A., Ryan, K. C., Putra, E. I., Saharjo, B. H., Nurhayati, A. D., Albar, I., Blake, D. R., Simpson, I. J., Stone, E. A., and Yokelson, R. J.: Field measurements of trace gases and aerosols emitted by peat fires in Central Kalimantan, Indonesia, during the 2015 El Niño, Atmos. Chem. Phys., 16, 11711–11732, https://doi.org/10.5194/acp-16-11711-2016, 2016.
Talbot, R. W., Beecher, K. M., Harriss, R. C., and Cofer, W. R.: Atmospheric
geochemistry of formic and acetic acids at a mid-latitude temperate site, J.
Geophys. Res.-Atmos., 93, 1638–1652, 1988.
Turetsky, M. R., Kane, E. S., Harden, J. W., Ottmar, R. D., Manies, K. L.,
Hoy, E., and Kasischke, E. S.: Recent acceleration of biomass burning and
carbon losses in Alaskan forests and peatlands, Nat. Geosci., 4, 27–31, 2011.
Urbanski, S. P.: Combustion efficiency and emission factors for wildfire-season fires in mixed conifer forests of the northern Rocky Mountains, US, Atmos. Chem. Phys., 13, 7241–7262, https://doi.org/10.5194/acp-13-7241-2013, 2013.
Waldrop, T. A. and Goodrick, S. L.: Introduction to prescribed fires in
Southern ecosystems, Science Update SRS-054, Asheville, NC: US Department of
Agriculture Forest Service, Southern Research Station, 80 p., 54, 1–80,
2012.
Ward, D., Susott, R., Kauffman, J., Babbitt, R., Cummings, D., Dias, B.,
Holben, B., Kaufman, Y., Rasmussen, R., and Setzer, A.: Smoke and fire
characteristics for cerrado and deforestation burns in Brazil: BASE-B
experiment, J. Geophys. Res.-Atmos. , 97, 14601–14619, 1992.
Ward, D. and Radke, L.: Emissions measurements from vegetation fires: A
comparative evaluation of methods and results, in: Fire in the Environment: The Ecological, Atmospheric, and Climatic
Importance of Vegetation Fires, edited by: Crutzen, P. J., Goldammer,
J. G., Dahlem Workshop Reports: Environmental
Sciences Research Report 13, John Wiley & Sons, Chischester,
53–76, 1993.
Ward, D. E. and Hao, W.: Projections of emissions from burning of biomass
for use in studies of global climate and atmospheric chemistry, Paper
91-128.4, Presented at the 84th Annual Meeting and Exhibition; Vancouver,
British Columbia; 16–21 June, Air and Waste Management Association, 16, 1991.
Ward, D. E. and Hardy, C. C.: Smoke emissions from wildland fires, Environ.
Int., 17, 117–134, 1991.
Ward, D. E., Hao, W. M., Susott, R. A., Babbitt, R. E., Shea, R. W.,
Kauffman, J. B., and Justice, C. O.: Effect of fuel composition on
combustion efficiency and emission factors for African savanna ecosystems,
J. Geophys. Res.-Atmos., 101, 23569–23576, 1996.
Weise, D. R., Fletcher, T. H., Johnson, T. J., Hao, W., Dietenberger, M.,
Princevac, M., Butler, B., McAllister, S., O'Brien, J., Loudermilk, L.,
Ottmar, R. D., Hudak, A., Kato, A., Shotorban, B., Mahalingam, S., and Mell,
W. E.: A project to measure and model pyrolysis to improve prediction of
prescribed fire behavior [Chapter 3], In: Advances in Forest
Fire Research 2018, edited by: Viegas, D. X., Coimbra, Portugal: Imprensa da Universidade de Coimbra,
308–218, 2018.
Wooster, M. J., Freeborn, P. H., Archibald, S., Oppenheimer, C., Roberts, G. J., Smith, T. E. L., Govender, N., Burton, M., and Palumbo, I.: Field determination of biomass burning emission ratios and factors via open-path FTIR spectroscopy and fire radiative power assessment: headfire, backfire and residual smouldering combustion in African savannahs, Atmos. Chem. Phys., 11, 11591–11615, https://doi.org/10.5194/acp-11-11591-2011, 2011.
Yashwanth, B., Shotorban, B., Mahalingam, S., Lautenberger, C., and Weise,
D.: A numerical investigation of the influence of radiation and moisture
content on pyrolysis and ignition of a leaf-like fuel element, Combust.
Flame, 163, 301–316, 2016.
Yokelson, R. J., Griffith, D. W. T., and Ward, D. E.: Open-path Fourier
transform infrared studies of large-scale laboratory biomass fires, J.
Geophys. Res.-Atmos., 101, 21067–21080, 1996.
Yokelson, R. J., Susott, R., Ward, D. E., Reardon, J., and Griffith, D. W.
T.: Emissions from smoldering combustion of biomass measured by open-path
Fourier transform infrared spectroscopy, J. Geophys. Res.-Atmos., 102,
18865–18877, 1997.
Yokelson, R. J., Goode, J. G., Ward, D. E., Susott, R. A., Babbitt, R. E.,
Wade, D. D., Bertschi, I., Griffith, D. W. T., and Hao, W. M.: Emissions of
formaldehyde, acetic acid, methanol, and other trace gases from biomass
fires in North Carolina measured by airborne Fourier transform infrared
spectroscopy, J. Geophys. Res.-Atmos., 104, 30109–30125, 1999.
Yokelson, R. J., Christian, T. J., Bertschi, I. T., and Hao, W. M.:
Evaluation of adsorption effects on measurements of ammonia, acetic acid,
and methanol, J. Geophys. Res.-Atmos., 108, 4649, https://doi.org/10.1029/2003JD003549, 2003.
Yokelson, R. J., Crounse, J. D., DeCarlo, P. F., Karl, T., Urbanski, S., Atlas, E., Campos, T., Shinozuka, Y., Kapustin, V., Clarke, A. D., Weinheimer, A., Knapp, D. J., Montzka, D. D., Holloway, J., Weibring, P., Flocke, F., Zheng, W., Toohey, D., Wennberg, P. O., Wiedinmyer, C., Mauldin, L., Fried, A., Richter, D., Walega, J., Jimenez, J. L., Adachi, K., Buseck, P. R., Hall, S. R., and Shetter, R.: Emissions from biomass burning in the Yucatan, Atmos. Chem. Phys., 9, 5785–5812, https://doi.org/10.5194/acp-9-5785-2009, 2009.
Yokelson, R. J., Burling, I. R., Gilman, J. B., Warneke, C., Stockwell, C. E., de Gouw, J., Akagi, S. K., Urbanski, S. P., Veres, P., Roberts, J. M., Kuster, W. C., Reardon, J., Griffith, D. W. T., Johnson, T. J., Hosseini, S., Miller, J. W., Cocker III, D. R., Jung, H., and Weise, D. R.: Coupling field and laboratory measurements to estimate the emission factors of identified and unidentified trace gases for prescribed fires, Atmos. Chem. Phys., 13, 89–116, https://doi.org/10.5194/acp-13-89-2013, 2013.
Young, V. L., Kieser, B. N., Chen, S. P., and Niki, H.: Seasonal trends and
local influences on nonmethane hydrocarbon concentrations in the Canadian
boreal forest, J. Geophys. Res.-Atmos., 102, 5913–5918, 1997.
Short summary
In this study we identify pyrolysis gases from prescribed burns conducted in pine forests using a manual extraction device. Captured gases were analyzed in the laboratory using infrared absorption spectroscopy. Results show that emission ratios relative to CO for ethene and acetylene were significantly greater than in previous fire studies, suggesting the sampling device was able to collect gases generated prior to ignition; this is corroborated by novel detections of five compounds via FTIR.
In this study we identify pyrolysis gases from prescribed burns conducted in pine forests using...
Altmetrics
Final-revised paper
Preprint