Articles | Volume 15, issue 6
https://doi.org/10.5194/acp-15-3527-2015
© Author(s) 2015. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
https://doi.org/10.5194/acp-15-3527-2015
© Author(s) 2015. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Research article
| 
31 Mar 2015
Research article |
| 31 Mar 2015
Influence of oil and gas field operations on spatial and temporal distributions of atmospheric non-methane hydrocarbons and their effect on ozone formation in winter
R. A. Field
CORRESPONDING AUTHOR
Department of Atmospheric Science, University of Wyoming, Laramie, WY, USA
J. Soltis
Department of Atmospheric Science, University of Wyoming, Laramie, WY, USA
M. C. McCarthy
Sonoma Technology Inc., Petaluma, CA, USA
S. Murphy
Department of Atmospheric Science, University of Wyoming, Laramie, WY, USA
D. C. Montague
Department of Atmospheric Science, University of Wyoming, Laramie, WY, USA
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Ground-based measurements of emissions from oil and natural gas production are important for understanding emission distributions and improving emission inventories. Here, measurement technique Other Test Method 33A (OTM 33A) is validated through several test releases staged at the Methane Emissions Technology Evaluation Center. These tests suggest OTM 33A has no inherent bias and that a group of OTM measurements is within 5 % of the known mean emission rate.
C. Warneke, P. Veres, S. M. Murphy, J. Soltis, R. A. Field, M. G. Graus, A. Koss, S.-M. Li, R. Li, B. Yuan, J. M. Roberts, and J. A. de Gouw
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Atmos. Chem. Phys., 14, 4909–4934, https://doi.org/10.5194/acp-14-4909-2014, https://doi.org/10.5194/acp-14-4909-2014, 2014
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The magnitude and evolution of Black Carbon (BC) and Brown Carbon (BrC) absorption with time remain unclear, causing uncertainty in climate models. Using data from the WE-CAN airborne measurement campaign, we show that absorption of BC from wildfire is relatively constant over time. BrC tends to be darker in more oxidated smoke plumes, challenging the idea that oxidation causes bleaching. We show that water-soluble BrC contributes 23 % of the total absorption at 660 nm.
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High wintertime ozone levels have occurred often in recent years in mountain basins with oil and gas production facilities. Photochemical modeling of ozone production serves as a basis for understanding the mechanism by which it occurs and for predictive capability. We present photochemical model simulations of ozone formation and accumulation in the Upper Green River basin, Wyoming, demonstrating the model's ability to simulate wintertime ozone and the sensitivity of ozone to its precursors.
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Rachel Edie, Anna M. Robertson, Robert A. Field, Jeffrey Soltis, Dustin A. Snare, Daniel Zimmerle, Clay S. Bell, Timothy L. Vaughn, and Shane M. Murphy
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Rudra P. Pokhrel, Eric R. Beamesderfer, Nick L. Wagner, Justin M. Langridge, Daniel A. Lack, Thilina Jayarathne, Elizabeth A. Stone, Chelsea E. Stockwell, Robert J. Yokelson, and Shane M. Murphy
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This study investigates enhancement of black carbon (BC) absorption in biomass burning emissions due to absorbing and non-absorbing coatings. The fraction of absorption due to BC, brown carbon (BrC), and lensing is estimated using different approaches. The similarities and differences between the results from these approaches are discussed. Absorption by BrC is shown to have good correlation with the elemental to organic carbon ratio (EC / OC) and AAE.
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C. Warneke, P. Veres, S. M. Murphy, J. Soltis, R. A. Field, M. G. Graus, A. Koss, S.-M. Li, R. Li, B. Yuan, J. M. Roberts, and J. A. de Gouw
Atmos. Meas. Tech., 8, 411–420, https://doi.org/10.5194/amt-8-411-2015, https://doi.org/10.5194/amt-8-411-2015, 2015
R. Li, C. Warneke, M. Graus, R. Field, F. Geiger, P. R. Veres, J. Soltis, S.-M. Li, S. M. Murphy, C. Sweeney, G. Pétron, J. M. Roberts, and J. de Gouw
Atmos. Meas. Tech., 7, 3597–3610, https://doi.org/10.5194/amt-7-3597-2014, https://doi.org/10.5194/amt-7-3597-2014, 2014
B. Rappenglück, L. Ackermann, S. Alvarez, J. Golovko, M. Buhr, R. A. Field, J. Soltis, D. C. Montague, B. Hauze, S. Adamson, D. Risch, G. Wilkerson, D. Bush, T. Stoeckenius, and C. Keslar
Atmos. Chem. Phys., 14, 4909–4934, https://doi.org/10.5194/acp-14-4909-2014, https://doi.org/10.5194/acp-14-4909-2014, 2014
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Subject: Gases | Research Activity: Field Measurements | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
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Ozone (O3) is a pollutant formed from the reactions of gases emitted from various sources. In urban areas, the density of human activities can increase the O3 formation rate (P(O3)); thus, impact air quality and health. Observations collected over Seoul, South Korea, are used to constrain P(O3). A high local P(O3) was found; however, local P(O3) was partly reduced due to compounds typically ignored. These observations also provide constraints for unmeasured compounds that will impact P(O3).
Romain Salignat, Matti Rissanen, Siddharth Iyer, Jean-Luc Baray, Pierre Tulet, Jean-Marc Metzger, Jérôme Brioude, Karine Sellegri, and Clémence Rose
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Delaney B. Kilgour, Gordon A. Novak, Megan S. Claflin, Brian M. Lerner, and Timothy H. Bertram
Atmos. Chem. Phys., 24, 3729–3742, https://doi.org/10.5194/acp-24-3729-2024, https://doi.org/10.5194/acp-24-3729-2024, 2024
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Xiangdong Zheng, Wen Yang, Yuting Sun, Chunmei Geng, Yingying Liu, and Xiaobin Xu
Atmos. Chem. Phys., 24, 3759–3768, https://doi.org/10.5194/acp-24-3759-2024, https://doi.org/10.5194/acp-24-3759-2024, 2024
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Chen et al. (2022) attributed the nocturnal ozone enhancement (NOE) during the night of 31 July 2021 in the North China Plain (NCP) to "the direct stratospheric intrusion to reach the surface". We analyzed in situ data from the NCP. Our results do not suggest that there was a significant impact from the stratosphere on surface ozone during the NOE. We argue that the NOE was not caused by stratospheric intrusion but originated from fresh photochemical production in the lower troposphere.
James M. Roberts, Siyuan Wang, Patrick R. Veres, J. Andrew Neuman, Michael A. Robinson, Ilann Bourgeois, Jeff Peischl, Thomas B. Ryerson, Chelsea R. Thompson, Hannah M. Allen, John D. Crounse, Paul O. Wennberg, Samuel R. Hall, Kirk Ullmann, Simone Meinardi, Isobel J. Simpson, and Donald Blake
Atmos. Chem. Phys., 24, 3421–3443, https://doi.org/10.5194/acp-24-3421-2024, https://doi.org/10.5194/acp-24-3421-2024, 2024
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We measured cyanogen bromide (BrCN) in the troposphere for the first time. BrCN is a product of the same active bromine chemistry that destroys ozone and removes mercury in polar surface environments and is a previously unrecognized sink for active Br compounds. BrCN has an apparent lifetime against heterogeneous loss in the range 1–10 d, so it serves as a cumulative marker of Br-radical chemistry. Accounting for BrCN chemistry is an important part of understanding polar Br cycling.
Kai Qin, Wei Hu, Qin He, Fan Lu, and Jason Blake Cohen
Atmos. Chem. Phys., 24, 3009–3028, https://doi.org/10.5194/acp-24-3009-2024, https://doi.org/10.5194/acp-24-3009-2024, 2024
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We compute CH4 emissions and uncertainty on a mine-by-mine basis, including underground, overground, and abandoned mines. Mine-by-mine gas and flux data and 30 min observations from a flux tower located next to a mine shaft are integrated. The observed variability and bias correction are propagated over the emissions dataset, demonstrating that daily observations may not cover the range of variability. Comparisons show both an emissions magnitude and spatial mismatch with current inventories.
Fan Zhang, Binyu Xiao, Zeyu Liu, Yan Zhang, Chongguo Tian, Rui Li, Can Wu, Yali Lei, Si Zhang, Xinyi Wan, Yubao Chen, Yong Han, Min Cui, Cheng Huang, Hongli Wang, Yingjun Chen, and Gehui Wang
EGUsphere, https://doi.org/10.5194/egusphere-2024-652, https://doi.org/10.5194/egusphere-2024-652, 2024
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Mandatory use of low-sulfur fuel according to global sulfur limit regulation leads to large uncertainty on VOCs emission. Therefore, on-board test of VOCs from 9 typical cargo ships in China were carried out. Results showed that the switch of fuels from heavy fuel oil to diesel increased EFVOCs by 48% on average, enhancing both O3 and secondary organic aerosol formation potentials. This indicated the implementation of globally ultra-low-sulfur oil policy in the near future needs to be optimized.
Jian Wang, Lei Xue, Qianyao Ma, Feng Xu, Gaobin Xu, Shibo Yan, Jiawei Zhang, Jianlong Li, Honghai Zhang, Guiling Zhang, and Zhaohui Chen
EGUsphere, https://doi.org/10.5194/egusphere-2023-2935, https://doi.org/10.5194/egusphere-2023-2935, 2024
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This study investigated the distribution and sources of non-methane hydrocarbons (NMHCs) in the lower atmosphere over the marginal seas of China. NMHCs, a subset of volatile organic compounds (VOCs), play a crucial role in atmospheric chemistry. Derived from systematic atmospheric sampling in coastal cities and marginal sea regions, this study offer valuable insights into the interaction between land and sea in shaping offshore atmospheric NMHCs.
Yao Yan Huang and D. James Donaldson
Atmos. Chem. Phys., 24, 2387–2398, https://doi.org/10.5194/acp-24-2387-2024, https://doi.org/10.5194/acp-24-2387-2024, 2024
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Ground-level ozone interacts at the lake–land boundary; this is important to our understanding and modelling of atmospheric chemistry and air pollution in the lower atmosphere. We show that a steep ozone gradient occurs year-round moving inland up to 1 km from the lake and that this gradient is influenced by seasonal factors on the local land environment, where more rural areas are more greatly affected seasonally.
Arpit Awasthi, Baerbel Sinha, Haseeb Hakkim, Sachin Mishra, Varkrishna Mummidivarapu, Gurmanjot Singh, Sachin D. Ghude, Vijay Kumar Soni, Narendra Nigam, Vinayak Sinha, and Madhavan N. Rajeevan
EGUsphere, https://doi.org/10.5194/egusphere-2024-501, https://doi.org/10.5194/egusphere-2024-501, 2024
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Our study uses a data set of 111 VOCs from a PTR-ToF-MS 10k, PM10 and PM2.5 in a PMF source-receptor model to resolve 11 pollution sources validated with chemical fingerprints collected at the source. Crop residue burning and heating contribute ~50 % of the PM, while traffic and industrial emissions dominate the gas-phase VOCs burden and SOA formation potential (>60 %). Non-tailpipe emissions from CNG powered commercial vehicles dominate the transport sector contribution to the PM burden.
Katrin Müller, Jordis S. Tradowsky, Peter von der Gathen, Christoph Ritter, Sharon Patris, Justus Notholt, and Markus Rex
Atmos. Chem. Phys., 24, 2169–2193, https://doi.org/10.5194/acp-24-2169-2024, https://doi.org/10.5194/acp-24-2169-2024, 2024
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The Palau Atmospheric Observatory is introduced as an ideal site to detect changes in atmospheric composition and dynamics above the remote tropical western Pacific. We focus on the ozone sounding program from 2016–2021, including El Niño 2016. The year-round high convective activity is reflected in dominant low tropospheric ozone and high relative humidity. Their seasonal distributions are unique compared to other tropical sites and are modulated by the Intertropical Convergence Zone.
Ziyan Guo, Keding Lu, Pengxiang Qiu, Mingyi Xu, and Zhaobing Guo
Atmos. Chem. Phys., 24, 2195–2205, https://doi.org/10.5194/acp-24-2195-2024, https://doi.org/10.5194/acp-24-2195-2024, 2024
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The formation of secondary sulfate needs to be further explored. In this work, we simultaneously measured sulfur and oxygen isotopic compositions to gain an increased understanding of specific sulfate formation processes. The results indicated that secondary sulfate was mainly ascribed to SO2 homogeneous oxidation by OH radicals and heterogeneous oxidation by H2O2 and Fe3+ / O2. This study is favourable for deeply investigating the sulfur cycle in the atmosphere.
Imran A. Girach, Narendra Ojha, Prabha R. Nair, Kandula V. Subrahmanyam, Neelakantan Koushik, Mohammed M. Nazeer, Nadimpally Kiran Kumar, Surendran Nair Suresh Babu, Jos Lelieveld, and Andrea Pozzer
Atmos. Chem. Phys., 24, 1979–1995, https://doi.org/10.5194/acp-24-1979-2024, https://doi.org/10.5194/acp-24-1979-2024, 2024
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We investigate surface ozone variability in East Antarctica based on measurements and EMAC global model simulations during austral summer. Nearly half of the surface ozone is found to be of stratospheric origin. The east coast of Antarctica acts as a stronger sink of ozone than surrounding regions. Photochemical loss of ozone is counterbalanced by downward transport of ozone. The study highlights the intertwined role of chemistry and dynamics in governing ozone variations over East Antarctica.
Ying Zhang, Duzitian Li, Xu-Cheng He, Wei Nie, Chenjuan Deng, Runlong Cai, Yuliang Liu, Yishuo Guo, Chong Liu, Yiran Li, Liangduo Chen, Yuanyuan Li, Chenjie Hua, Tingyu Liu, Zongcheng Wang, Jiali Xie, Lei Wang, Tuukka Petäjä, Federico Bianchi, Ximeng Qi, Xuguang Chi, Pauli Paasonen, Yongchun Liu, Chao Yan, Jingkun Jiang, Aijun Ding, and Markku Kulmala
Atmos. Chem. Phys., 24, 1873–1893, https://doi.org/10.5194/acp-24-1873-2024, https://doi.org/10.5194/acp-24-1873-2024, 2024
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This study conducts a long-term observation of gaseous iodine oxoacids in two Chinese megacities, revealing their ubiquitous presence with peak concentrations (up to 0.1 pptv) in summer. Our analysis suggests a mix of terrestrial and marine sources for iodine. Additionally, iodic acid is identified as a notable contributor to sub-3 nm particle growth and particle survival probability.
Xinyuan Zhang, Lingling Wang, Nan Wang, Shuangliang Ma, Shenbo Wang, Ruiqin Zhang, Dong Zhang, Mingkai Wang, and Hongyu Zhang
EGUsphere, https://doi.org/10.5194/egusphere-2023-2913, https://doi.org/10.5194/egusphere-2023-2913, 2024
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Online observational data on particulate matter composition, gaseous pollutants, and meteorological conditions from ten sites in China before and during the COVID-19 pandemic were analyzed to investigate the variation in NH3 concentrations and particle pH and explore the promoting effect of increased pH values on HONO formation. This is the first study to discuss the reasons for the increase in AOC during the pandemic from the perspective of the influence of NH3 on HONO.
Guoxian Zhang, Renzhi Hu, Pinhua Xie, Changjin Hu, Xiaoyan Liu, Liujun Zhong, Haotian Cai, Bo Zhu, Shiyong Xia, Xiaofeng Huang, Xin Li, and Wenqing Liu
Atmos. Chem. Phys., 24, 1825–1839, https://doi.org/10.5194/acp-24-1825-2024, https://doi.org/10.5194/acp-24-1825-2024, 2024
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Comprehensive observation of HOx radicals was conducted at a coastal site in the Pearl River Delta. Radical chemistry was influenced by different air masses in a time-dependent way. Land mass promotes a more active photochemical process, with daily averages of 7.1 × 106 and 5.2 × 108 cm−3 for OH and HO2 respectively. The rapid oxidation process was accompanied by a higher diurnal HONO concentration, which influences the ozone-sensitive system and eventually magnifies the background ozone.
Sarah Albertin, Joël Savarino, Slimane Bekki, Albane Barbero, Roberto Grilli, Quentin Fournier, Irène Ventrillard, Nicolas Caillon, and Kathy Law
Atmos. Chem. Phys., 24, 1361–1388, https://doi.org/10.5194/acp-24-1361-2024, https://doi.org/10.5194/acp-24-1361-2024, 2024
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This study reports the first simultaneous records of oxygen (Δ17O) and nitrogen (δ15N) isotopes in nitrogen dioxide (NO2) and nitrate (NO3−). These data are combined with atmospheric observations to explore sub-daily N reactive chemistry and quantify N fractionation effects in an Alpine winter city. The results highlight the necessity of using Δ17O and δ15N in both NO2 and NO3− to avoid biased estimations of NOx sources and fates from NO3− isotopic records in urban winter environments.
Shigeyuki Ishidoya, Kazuhiro Tsuboi, Hiroaki Kondo, Kentaro Ishijima, Nobuyuki Aoki, Hidekazu Matsueda, and Kazuyuki Saito
Atmos. Chem. Phys., 24, 1059–1077, https://doi.org/10.5194/acp-24-1059-2024, https://doi.org/10.5194/acp-24-1059-2024, 2024
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A method evaluating techniques for carbon neutrality, such as carbon capture and storage (CCS), is important. This study presents a method to evaluate CO2 emissions from a cement plant based on atmospheric O2 and CO2 measurements. The method will also be useful for evaluating CO2 capture from flue gas at CCS plants, since the plants remove CO2 from the atmosphere without causing any O2 changes, just as cement plants do, differing only in the direction of CO2 exchange with the atmosphere.
Magdalena Pühl, Anke Roiger, Alina Fiehn, Alan M. Gorchov Negron, Eric A. Kort, Stefan Schwietzke, Ignacio Pisso, Amy Foulds, James Lee, James L. France, Anna E. Jones, Dave Lowry, Rebecca E. Fisher, Langwen Huang, Jacob Shaw, Prudence Bateson, Stephen Andrews, Stuart Young, Pamela Dominutti, Tom Lachlan-Cope, Alexandra Weiss, and Grant Allen
Atmos. Chem. Phys., 24, 1005–1024, https://doi.org/10.5194/acp-24-1005-2024, https://doi.org/10.5194/acp-24-1005-2024, 2024
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In April–May 2019 we carried out an airborne field campaign in the southern North Sea with the aim of studying methane emissions of offshore gas installations. We determined methane emissions from elevated methane measured downstream of the sampled installations. We compare our measured methane emissions with estimated methane emissions from national and global annual inventories. As a result, we find inconsistencies of inventories and large discrepancies between measurements and inventories.
Georgios I. Gkatzelis, Matthew M. Coggon, Chelsea E. Stockwell, Rebecca S. Hornbrook, Hannah Allen, Eric C. Apel, Megan M. Bela, Donald R. Blake, Ilann Bourgeois, Steven S. Brown, Pedro Campuzano-Jost, Jason M. St. Clair, James H. Crawford, John D. Crounse, Douglas A. Day, Joshua P. DiGangi, Glenn S. Diskin, Alan Fried, Jessica B. Gilman, Hongyu Guo, Johnathan W. Hair, Hannah S. Halliday, Thomas F. Hanisco, Reem Hannun, Alan Hills, L. Gregory Huey, Jose L. Jimenez, Joseph M. Katich, Aaron Lamplugh, Young Ro Lee, Jin Liao, Jakob Lindaas, Stuart A. McKeen, Tomas Mikoviny, Benjamin A. Nault, J. Andrew Neuman, John B. Nowak, Demetrios Pagonis, Jeff Peischl, Anne E. Perring, Felix Piel, Pamela S. Rickly, Michael A. Robinson, Andrew W. Rollins, Thomas B. Ryerson, Melinda K. Schueneman, Rebecca H. Schwantes, Joshua P. Schwarz, Kanako Sekimoto, Vanessa Selimovic, Taylor Shingler, David J. Tanner, Laura Tomsche, Krystal T. Vasquez, Patrick R. Veres, Rebecca Washenfelder, Petter Weibring, Paul O. Wennberg, Armin Wisthaler, Glenn M. Wolfe, Caroline C. Womack, Lu Xu, Katherine Ball, Robert J. Yokelson, and Carsten Warneke
Atmos. Chem. Phys., 24, 929–956, https://doi.org/10.5194/acp-24-929-2024, https://doi.org/10.5194/acp-24-929-2024, 2024
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This study reports emissions of gases and particles from wildfires. These emissions are related to chemical proxies that can be measured by satellite and incorporated into models to improve predictions of wildfire impacts on air quality and climate.
Jie Wang, Haichao Wang, Yee Jun Tham, Lili Ming, Zelong Zheng, Guizhen Fang, Cuizhi Sun, Zhenhao Ling, Jun Zhao, and Shaojia Fan
Atmos. Chem. Phys., 24, 977–992, https://doi.org/10.5194/acp-24-977-2024, https://doi.org/10.5194/acp-24-977-2024, 2024
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Many works report NO3 chemistry in inland regions while less target marine regions. We measured N2O5 and related species on a typical island and found intensive nighttime chemistry and rapid NO3 loss. NO contributed significantly to NO3 loss despite its sub-ppbv level, suggesting nocturnal NO3 reactions would be largely enhanced once free from NO emissions in the open ocean. This highlights the strong influences of urban outflow on downward marine areas in terms of nighttime chemistry.
Jun Zhou, Chunsheng Zhang, Aiming Liu, Bin Yuan, Yan Wang, Wenjie Wang, Jie-Ping Zhou, Yixin Hao, Xiao-Bing Li, Xianjun He, Xin Song, Yubin Chen, Suxia Yang, Shuchun Yang, Yanfeng Wu, Bin Jiang, Shan Huang, Junwen Liu, Jipeng Qi, Minhui Deng, Yibo Huangfu, and Min Shao
EGUsphere, https://doi.org/10.5194/egusphere-2023-2230, https://doi.org/10.5194/egusphere-2023-2230, 2024
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In-depth understanding of near-ground vertical and temporal photochemical ozone (O3) formation is crucial for mitigating O3 pollution. By utilizing a self-built vertical observation system, a direct net photochemical O3 production rate detection system, and an observation-based model, we have diagnosed the vertical distributions and formation mechanism of net photochemical O3 production rates and sensitivity in Pearl River Delta region, one of the most O3 polluted area in China.
Tanja J. Schuck, Johannes Degen, Eric Hintsa, Peter Hoor, Markus Jesswein, Timo Keber, Daniel Kunkel, Fred Moore, Florian Obersteiner, Matt Rigby, Thomas Wagenhäuser, Luke M. Western, Andreas Zahn, and Andreas Engel
Atmos. Chem. Phys., 24, 689–705, https://doi.org/10.5194/acp-24-689-2024, https://doi.org/10.5194/acp-24-689-2024, 2024
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We study the interhemispheric gradient of sulfur hexafluoride (SF6), a strong long-lived greenhouse gas. Its emissions are stronger in the Northern Hemisphere; therefore, mixing ratios in the Southern Hemisphere lag behind. Comparing the observations to a box model, the model predicts air in the Southern Hemisphere to be older. For a better agreement, the emissions used as model input need to be increased (and their spatial pattern changed), and we need to modify north–south transport.
Jérémy Gueffier, François Gheusi, Marie Lothon, Véronique Pont, Alban Philibert, Fabienne Lohou, Solène Derrien, Yannick Bezombes, Gilles Athier, Yves Meyerfeld, Antoine Vial, and Emmanuel Leclerc
Atmos. Chem. Phys., 24, 287–316, https://doi.org/10.5194/acp-24-287-2024, https://doi.org/10.5194/acp-24-287-2024, 2024
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This study investigates the link between weather regime and atmospheric composition at a Pyrenean observatory. Five years of meteorological data were synchronized on a daily basis and then, using a clustering method, separated into six groups of observation days, with most showing marked characteristics of different weather regimes (fair and disturbed weather, winter windstorms, foehn). Statistical differences in gas and particle concentrations appeared between the groups and are discussed.
Yusheng Zhang, Feixue Zheng, Zemin Feng, Chaofan Lian, Weigang Wang, Xiaolong Fan, Wei Ma, Zhuohui Lin, Chang Li, Gen Zhang, Chao Yan, Ying Zhang, Veli-Matti Kerminen, Federico Bianch, Tuukka Petäjä, Juha Kangasluoma, Markku Kulmala, and Yongchun Liu
EGUsphere, https://doi.org/10.5194/egusphere-2023-3139, https://doi.org/10.5194/egusphere-2023-3139, 2024
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In this study, HONO budget has been validated during COVID-19 lockdown event. Main conclusions are as follows: 1. HONO concentrations show a significant decrease from 0.97 to 0.53ppb during lockdown. 2. Vehicle emissions accounted for 53% of nighttime sources. The heterogeneous conversion of NO2 on ground surfaces important (31%) than aerosol (2%). 3. Daytime dominant source shifts from the homogenous reaction between NO and OH (51%) to photolysis of nitrate photolysis (53%) during the lockdown.
Dong Zhang, Xiao Li, Minghao Yuan, Yifei Xu, Qixiang Xu, Fangcheng Su, Shenbo Wang, and Ruiqin Zhang
EGUsphere, https://doi.org/10.5194/egusphere-2023-2835, https://doi.org/10.5194/egusphere-2023-2835, 2024
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In recent years, Zhengzhou's O3 pollution has increasingly intensified, becoming one of the cities with the highest O3 pollution in central China. During the observation period, ethane, acetone, and propane were always the most abundant species. Vehicular exhaust, solvent usage, and industrial production were the main emission sources of VOCs. According to the scenario analysis, the minimum reduction ratio of AVOCs/NOx should be no less than 3:1 to reduce O3 production.
Nathaniel Brockway, Peter K. Peterson, Katja Bigge, Kristian D. Hajny, Paul B. Shepson, Kerri A. Pratt, Jose D. Fuentes, Tim Starn, Robert Kaeser, Brian H. Stirm, and William R. Simpson
Atmos. Chem. Phys., 24, 23–40, https://doi.org/10.5194/acp-24-23-2024, https://doi.org/10.5194/acp-24-23-2024, 2024
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Bromine monoxide (BrO) strongly affects atmospheric chemistry in the springtime Arctic, yet there are still many uncertainties around its sources and recycling, particularly in the context of a rapidly changing Arctic. In this study, we observed BrO as a function of altitude above the Alaskan Arctic. We found that BrO was often most concentrated near the ground, confirming the ability of snow to produce and recycle reactive bromine, and identified four common vertical distributions of BrO.
Alina Fiehn, Maximilian Eckl, Julian Kostinek, Michał Gałkowski, Christoph Gerbig, Michael Rothe, Thomas Röckmann, Malika Menoud, Hossein Maazallahi, Martina Schmidt, Piotr Korbeń, Jarosław Neçki, Mila Stanisavljević, Justyna Swolkień, Andreas Fix, and Anke Roiger
Atmos. Chem. Phys., 23, 15749–15765, https://doi.org/10.5194/acp-23-15749-2023, https://doi.org/10.5194/acp-23-15749-2023, 2023
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During the CoMet mission in the Upper Silesian Coal Basin (USCB) ground-based and airborne air samples were taken and analyzed for the isotopic composition of CH4 to derive the mean signature of the USCB and source signatures of individual coal mines. Using δ2H signatures, the biogenic emissions from the USCB account for 15 %–50 % of total emissions, which is underestimated in common emission inventories. This demonstrates the importance of δ2H-CH4 observations for methane source apportionment.
Yifei Song, Chaoyang Xue, Yuanyuan Zhang, Pengfei Liu, Fengxia Bao, Xuran Li, and Yujing Mu
Atmos. Chem. Phys., 23, 15733–15747, https://doi.org/10.5194/acp-23-15733-2023, https://doi.org/10.5194/acp-23-15733-2023, 2023
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We present measurements of HONO flux and related parameters over an agricultural field during a whole growing season of summer maize. This dataset allows studies on the characteristics and influencing factors of soil HONO emissions, determination of HONO emission factors, estimation of total HONO emissions at a national scale, and the discussion on future environmental policies in terms of mitigating regional air pollution.
Can Ye, Keding Lu, Xuefei Ma, Wanyi Qiu, Shule Li, Xinping Yang, Chaoyang Xue, Tianyu Zhai, Yuhan Liu, Xuan Li, Yang Li, Haichao Wang, Zhaofeng Tan, Xiaorui Chen, Huabin Dong, Limin Zeng, Min Hu, and Yuanhang Zhang
Atmos. Chem. Phys., 23, 15455–15472, https://doi.org/10.5194/acp-23-15455-2023, https://doi.org/10.5194/acp-23-15455-2023, 2023
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In this study, combining comprehensive field measurements and a box model, we found NO2 conversion on the ground surface was the most important source for HONO production among the proposed heterogeneous and gas-phase HONO sources. In addition, HONO was found to evidently enhance O3 production and aggravate O3 pollution in summer in China. Our study improved our understanding of the relative importance of different HONO sources and the crucial role of HONO in O3 formation in polluted areas.
Yann Cohen, Didier Hauglustaine, Bastien Sauvage, Susanne Rohs, Patrick Konjari, Ulrich Bundke, Andreas Petzold, Valérie Thouret, Andreas Zahn, and Helmut Ziereis
Atmos. Chem. Phys., 23, 14973–15009, https://doi.org/10.5194/acp-23-14973-2023, https://doi.org/10.5194/acp-23-14973-2023, 2023
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The upper troposphere–lower stratosphere (UTLS) is a key region regarding the lower atmospheric composition. This study consists of a comprehensive evaluation of an up-to-date chemistry–climate model in this layer, using regular in situ measurements based on passenger aircraft. For this purpose, a specific software (Interpol-IAGOS) has been updated and made publicly available. The model reproduces the carbon monoxide peaks due to biomass burning over the continental tropics particularly well.
Yifan Jiang, Men Xia, Zhe Wang, Penggang Zheng, Yi Chen, and Tao Wang
Atmos. Chem. Phys., 23, 14813–14828, https://doi.org/10.5194/acp-23-14813-2023, https://doi.org/10.5194/acp-23-14813-2023, 2023
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This study provides the first estimate of high rates of formic acid (HCOOH) production from the photochemical aging of real ambient particles and demonstrates the potential importance of this pathway in the formation of HCOOH under ambient conditions. Incorporating this pathway significantly improved the performance of a widely used chemical model. Our solution irradiation experiments demonstrated the importance of nitrate photolysis in HCOOH production via the production of oxidants.
Xuelian Zhong, Hengqing Shen, Min Zhao, Ji Zhang, Yue Sun, Yuhong Liu, Yingnan Zhang, Ye Shan, Hongyong Li, Jiangshan Mu, Yu Yang, Yanqiu Nie, Jinghao Tang, Can Dong, Xinfeng Wang, Yujiao Zhu, Mingzhi Guo, Wenxing Wang, and Likun Xue
Atmos. Chem. Phys., 23, 14761–14778, https://doi.org/10.5194/acp-23-14761-2023, https://doi.org/10.5194/acp-23-14761-2023, 2023
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Nitrous acid (HONO) is vital for atmospheric oxidation. In research at Mount Lao, China, models revealed a significant unidentified marine HONO source. Overlooking this could skew our understanding of air quality and climate change. This finding emphasizes HONO’s importance in the coastal atmosphere, uncovering previously unnoticed interactions.
Steven Job Thomas, Toni Tykkä, Heidi Hellén, Federico Bianchi, and Arnaud P. Praplan
Atmos. Chem. Phys., 23, 14627–14642, https://doi.org/10.5194/acp-23-14627-2023, https://doi.org/10.5194/acp-23-14627-2023, 2023
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The study employed total ozone reactivity to demonstrate how emissions of Norway spruce readily react with ozone and could be a major ozone sink, particularly under stress. Additionally, this approach provided insight into the limitations of current analytical techniques that measure the compounds present or emitted into the atmosphere. The study shows how the technique used was not enough to measure all compounds emitted, and this could potentially underestimate various atmospheric processes.
Jinsol Kim, John B. Miller, Charles E. Miller, Scott J. Lehman, Sylvia E. Michel, Vineet Yadav, Nick E. Rollins, and William M. Berelson
Atmos. Chem. Phys., 23, 14425–14436, https://doi.org/10.5194/acp-23-14425-2023, https://doi.org/10.5194/acp-23-14425-2023, 2023
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In this study, we present the partitioning of CO2 signals from biogenic, petroleum and natural gas sources by combining CO, 13CO2 and 14CO2 measurements. Using measurements from flask air samples at three sites in the greater Los Angeles region, we find larger and positive contributions of biogenic signals in winter and smaller and negative contributions in summer. The largest contribution of natural gas combustion generally occurs in summer.
Robert Woodward-Massey, Roberto Sommariva, Lisa K. Whalley, Danny R. Cryer, Trevor Ingham, William J. Bloss, Stephen M. Ball, Sam Cox, James D. Lee, Chris P. Reed, Leigh R. Crilley, Louisa J. Kramer, Brian J. Bandy, Grant L. Forster, Claire E. Reeves, Paul S. Monks, and Dwayne E. Heard
Atmos. Chem. Phys., 23, 14393–14424, https://doi.org/10.5194/acp-23-14393-2023, https://doi.org/10.5194/acp-23-14393-2023, 2023
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Measurements of OH, HO2 and RO2 radicals and also OH reactivity were made at a UK coastal site and compared to calculations from a constrained box model utilising the Master Chemical Mechanism. The model agreement displayed a strong dependence on the NO concentration. An experimental budget analysis for OH, HO2, RO2 and total ROx demonstrated significant imbalances between HO2 and RO2 production rates. Ozone production rates were calculated from measured radicals and compared to modelled values.
Leonard Kirago, Örjan Gustafsson, Samuel Mwaniki Gaita, Sophie L. Haslett, Michael J. Gatari, Maria Elena Popa, Thomas Röckmann, Christoph Zellweger, Martin Steinbacher, Jörg Klausen, Christian Félix, David Njiru, and August Andersson
Atmos. Chem. Phys., 23, 14349–14357, https://doi.org/10.5194/acp-23-14349-2023, https://doi.org/10.5194/acp-23-14349-2023, 2023
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This study provides ground-observational evidence that supports earlier suggestions that savanna fires are the main emitters and modulators of carbon monoxide gas in Africa. Using isotope-based techniques, the study has shown that about two-thirds of this gas is emitted from savanna fires, while for urban areas, in this case Nairobi, primary sources approach 100 %. The latter has implications for air quality policy, suggesting primary emissions such as traffic should be targeted.
Clara M. Nussbaumer, Bryan K. Place, Qindan Zhu, Eva Y. Pfannerstill, Paul Wooldridge, Benjamin C. Schulze, Caleb Arata, Ryan Ward, Anthony Bucholtz, John H. Seinfeld, Allen H. Goldstein, and Ronald C. Cohen
Atmos. Chem. Phys., 23, 13015–13028, https://doi.org/10.5194/acp-23-13015-2023, https://doi.org/10.5194/acp-23-13015-2023, 2023
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NOx is a precursor to hazardous tropospheric ozone and can be emitted from various anthropogenic sources. It is important to quantify NOx emissions in urban environments to improve the local air quality, which still remains a challenge, as sources are heterogeneous in space and time. In this study, we calculate NOx emissions over Los Angeles, based on aircraft measurements in June 2021, and compare them to a local emission inventory, which we find mostly overpredicts the measured values.
Cited articles
Adgate, J. L., Goldstein, B. D., and McKenzie, L. M.: Potential public health hazards, exposures and health effects from unconventional natural gas development, Environ. Sci. Technol., 48, 8307–8320, https://doi.org/10.1021/es404621d, 2014.
Ahmadov, R., McKeen, S., Trainer, M., Banta, R., Brewer, A., Brown, S., Edwards, P. M., de Gouw, J. A., Frost, G. J., Gilman, J., Helmig, D., Johnson, B., Karion, A., Koss, A., Langford, A., Lerner, B., Olson, J., Oltmans, S., Peischl, J., Pétron, G., Pichugina, Y., Roberts, J. M., Ryerson, T., Schnell, R., Senff, C., Sweeney, C., Thompson, C., Veres, P. R., Warneke, C., Wild, R., Williams, E. J., Yuan, B., and Zamora, R.: Understanding high wintertime ozone pollution events in an oil- and natural gas-producing region of the western US, Atmos. Chem. Phys., 15, 411–429, https://doi.org/10.5194/acp-15-411-2015, 2015.
Allen, D. T., Torres, V. M., Thomas, J., Sullivan, D. W., Harrison, M., Hendler, A., Herndon, S. C., Kolb, C. E., Fraser, M. P., Hill, A. D., Lamb, B. K., Miskimins, J., Sawyer, R. F., and Seinfeld, J. H.: Measurements of methane emissions at natural gas production sites in the United States, P. Natl. Acad. Sci., 110, 17768–17773, https://doi.org/10.1073/pnas.1304880110, 2013.
Atkinson, R.: Kinetics and mechanisms of the gas-phase reactions of the hydroxyl radical with organic-compounds under atmospheric conditions, Chem. Rev., 86, 69–201, 1986.
Atkinson, R.: Gas-phase tropospheric chemistry of organic compounds. A review, Atmos. Environ., 24A, 1–41, 1990.
Atkinson, R. and Arey, J.: Atmospheric degradation of volatile organic compounds, Chem. Rev., 103, 4605–4638, 2003.
Atkinson, R. and Aschmann, S. M.: Kinetics of the reactions of acenaphthene and acenaphthylene and structurally related aromatic compounds with OH and NO3 radicals, N2O5 and O3 at 296 ± 2 K, Int. J. Chem. Kinet., 20, 513–539,1988.
Brandt, A. R., Heath, G. A., Kort, E. A., O'Sullivan, F. O., Pétron, G., Jordaan, S. M., Tans, P., Wilcox, J., Gopstein, A. M., Arent, D., Wofsy, S., Brown, N. J., Bardley, R., Stucky, G. D., Eardley, D., and Harris, R.: Methane leaks from North American natural gas systems, Science, 343, 733–735, 2014.
Broadway, G. and Tipler, A.: Ozone precursor analysis using a Thermal Desorption-GC system, PerkinElmer Gas Chromatography White Paper No. 008880B_01, Perkin Elmer, 2012.
Brown, S. G., Frankel, A., and Hafner, H. R.: Source apportionment of VOCs in the Los Angeles area using positive matrix factorization, Atmos. Environ., 41, 227–237, 2007.
Buzcu, B. and Fraser, M. P.: Comparison of VOC emissions inventory data with source apportionment results for Houston, TX, Atmos. Environ., 42, 5032–5043, 2008.
Carter, W. P. and Seinfeld, J. H.: Winter ozone formation and VOC incremental reactivities in the Upper Green River Basin of Wyoming, Atmos. Environ., 50, 255–266, 2012.
Caulton, D. R., Shepson, P. B., Santoro, R. L., Sparks, J. P., Howarth, R. W., Ingraffea, A. R., Cambaliza, M. O. L., Sweeney, C., Davis, K. J., Stirm, B. H., Montzka, S. A., and Miller, B. R.: Toward a better understanding and quantification of methane emissions from shale gas development, P. Natl. Acad. Sci., 111, 6237–6242, 2014.
Colburn, T., Schultz, K., Herrick, L., and Kwiatkowski, C.: An exploratory study of air quality near natural gas operations, Hum. Ecol. Risk Assess. Int. J., 20, 86–105, https://doi.org/10.1080/10807039.2012.749447, 2014.
Cox, L. and Schafer, L.: A working model for oil and gas produced water treatment. Energy resources and produced waters conference, 25 to 26 May 2010, Laramie Wyoming, accessed through the University of Wyoming WyoCast On-Demand interface at: http://wyocast.uwyo.edu/WyoCast/Play/27449dccec254addb46c72528606a76d (last access: 1 September 2014), 2010.
DeMore, W. B., Sander, S. P., Golden, D. M., Hampson, R. F., Kurylo, M. J., Howard, C. J., Ravishankara, A. R., Kolb, C. E., and Molina, M. J.: Chemical kinetics and photochemical data for use in stratospheric modeling: Evaluation number 12, JPL Publ. 97–4, 1–266, NASA, Pasadena, California, 1997.
Dernie, J. and Dumitrean, P.: UK hydrocarbon network annual report for 2012, Report by AEA Technology ED 47833/ED46645, 2013.
Derwent, R. G., Dernie, J., Dollard, G. J., Dumitrean, P., Mitchell, R. F., Murrells, T. P., Telling, S. P., and Field, R. A.: Twenty years of continuous high time resolution volatile organic compound monitoring in the United kingdom from 1993 to 2012, Atmos. Environ., 99, 239–247, 2014.
Dollard, G. J., Davies, T. J., Jones, B. M. R., Nason, P. D., Chandler, J., Dumitrean, P., Delaney, M., Watkins, D., and Field, R. A.: The UK hydrocarbon monitoring network, Chap. 3, 37–50, Volatile organic compounds in the atmosphere, ISBN 0-85404-215-61995, edited by: Hester, R. E. and Harrison, R. M., Royal Society of Chemistry, Cambridge, UK, 1995.
Edwards, P. M., Young, C. J., Aikin, K., deGouw, J., Dubé, W. P., Geiger, F., Gilman, J., Helmig, D., Holloway, J. S., Kercher, J., Lerner, B., Martin, R., McLaren, R., Parrish, D. D., Peischl, J., Roberts, J. M., Ryerson, T. B., Thornton, J., Warneke, C., Williams, E. J., and Brown, S. S.: Ozone photochemistry in an oil and natural gas extraction region during winter: simulations of a snow-free season in the Uintah Basin, Utah, Atmos. Chem. Phys., 13, 8955–8971, https://doi.org/10.5194/acp-13-8955-2013, 2013.
Edwards, P. M., Brown, S. S., Roberts, J. M., Ahmadov, R., Banta, R. M, de Gouw, J. A., Dubeì, W. P., Field, R. A., Flynn, J. H., Gilman, J. B., Graus, M., Helmig, D., Koss, A., Langford, A. O., Lefer, B. L., Lerner, B. M., Li, R., Li, S. M., McKeen, S. A., Murphy, S. M., Parrish, D. D., Senff, C. J., Soltis, J., Stutz, J., Sweeney, C., Thompson, C. R., Trainer, M. K., Tsai, C., Veres, P. R., Washenfelder, R. A., Warneke, C., Wild, R. J., Young, C. J., Yuan, B., and Zamora, R.: Unconventional photochemistry underlying winter ozone in an oil and gas producing region, Nature, 514, 351–354, https://doi.org/10.1038/nature13767, 2014.
Efron, B.: The jackknife, the bootstrap and other resampling plans, Society for Industrial and Applied Mathematics, Philadelphia, PA, ISBN 978-0-89871-179-0, 1982.
Efron, B. and Tibshirani, R. J.: An introduction to the bootstrap, Chapman & Hall, New York, ISBN-13: 978-041204231, 1993.
Emery, B.: An analysis of wintertime surface wind fields in the Upper Green River Basin of Sublette County, Wyoming, University of Wyoming ProQuest Dissertations and Theses, Publication Number AAT 1543752, ISBN 9781303315442, available at: http://www.proquest.com/products-services/dissertations/, Thesis (M.S.), 2013.
Field, R. A., Soltis, J., and Murphy, S.: Air quality concerns of unconventional oil and natural gas production, Environ. Sci. Processes Impacts, 16, 954–969, 2014.
Francis, R.: Personal Communication regarding performance of Thermo Scientific model 55i analyzer, Thermo Scientific, 2014.
Gilman, J. B., Kuster, W. C., Goldan, P. D., Herndon, S. C., Zahniser, M. S., Tucker, S. C., Brewer, W. A., Lerner, B. M., Williams, E. J., Harley, R. A., Fehsenfeld, F. C., Warneke, C., and de Gouw, J. A.: Measurements of volatile organic compounds during the 2006 TexAQS/GoMACCS campaign: Industrial influences, regional characteristics, and diurnal dependencies of the OH reactivity, J. Geophys. Res., 114, D00F06, https://doi.org/10.1029/2008JD011525, 2009.
Gilman, J. B., Lerner, B. M., Kuster, W. C., and de Gouw, J. A.: Source signature of volatile organic compounds from oil and natural gas operations in Northeastern Colorado, Environ. Sci. Technol., 47, 1297–1305, 2013.
Helmig, D., Thompson, C. R., Evans, J., Boylan, P., Hueber, J., and Park, J.-H.: Highly elevated atmospheric levels of volatile organic compounds in the Uintah Basin, Utah, Environ. Sci. Technol., 48, 4707–4715, 2014.
Karion, A., Sweeney, C., Pétron, G., Frost, G., Hardesty, R. M., Kofler, J., Miller, B. R., Newberger, T., Wolter, S., Banta, R., Brewer, A., Dlugokencky, E. J., Lang, P. M., Montzka, S. A., Schnell, R., Tans, P., Trainer, M., Zamora, R., and Conley, S.: Methane emissions estimate from airborne measurements over a western United States natural gas field, Geophys. Res. Lett., 40, 4393–4397, https://doi.org/10.1002/grl.50811, 2013.
Litovitz, A., Cutright, A., Abramzon, S., Burger, N., and Samaras, C.: Estimation of regional air-quality damages from Marcellus Shale natural gas extraction in Pennsylvania, Environ. Res. Lett., 8, 014017, https://doi.org/10.1088/1748-9326/8/1/014017, 2013.
Martin, R., Moore, K., Mansfield, M., Hill, S., Harper, K., and Shorthill, H.: Uintah Basin winter ozone and air quality study, Report, University of Utah, available at: http://rd.usu.edu/files/uploads/ubos_2010-11_final_report.pdf (last access: 14 August 2014), 2011.
McCarthy, M. C., Aklilu, Y. A., Brown, S. G., and Lyder, D. A.: Source apportionment of volatile organic compounds measured in Edmonton, Alberta, Atmos. Environ., 81, 504–516, 2013.
McKenzie, L. M., Witter, R. Z., Newman, L. S., and Adgate, J. L.: Human health risk assessment of air emissions from development of unconventional natural gas resources, Sci. Total Environ., 424, 79–87, 2012.
McKenzie, L. M., Guo, R., Witter, R. Z., Savitz, D. A., Newman, L. S., and Adgate, J. L.: Birth outcomes and maternal residential proximity to natural gas development in rural Colorado, Environ. Health. Persp., 122, 412–417, 2014.
Moore, C. W., Zielinska, B., Pétron, G., and Jackson, R. B.: Air impacts of increased natural gas acquisition, processing, and use: a critical review, Environ. Sci. Technol., 48, 8349–8359, https://doi.org/10.1021/es4053472, 2014.
MSI (Meteorological Solutions, Inc.): Final Report, 2011 Upper Green River Winter Ozone Study, available at: http://sgirt.webfactional.com/filesearch/content/Air Quality Division/Programs/Ozone/Winter Ozone-Winter Ozone Study/2011_UGWOS-Monitoring-Final-Report.pdf, Report, 2011.
MSI (Meteorological Solutions, Inc.): Final Report, 2012 Upper Green River Winter Ozone Study, available at: http://sgirt.webfactional.com/filesearch/content/Air Quality Division/Programs/Ozone/Winter Ozone-Winter Ozone Study/2012_UGWOS-Monitoring-Final-Report.pdf, Report, 2012.
MSI (Meteorological Solutions, Inc.): Final Report, 2013 Upper Green River Winter Ozone Study, MSI and T&B Systems, available at: http://sgirt.webfactional.com/filesearch/content/Air Quality Division/Programs/Ozone/Winter Ozone-Winter Ozone Study/2013_UGWOS-Monitoring-Final-Report.pdf, Report, 2013.
MSI (Meteorological Solutions, Inc.): Final Report, 2014 Upper Green River Winter Ozone Study, available at: http://sgirt.webfactional.com/filesearch/content/Air Quality Division/Programs/Ozone/Winter Ozone-Winter Ozone Study/2014_UGWOS-Monitoring-Final-Report.pdf, Report, 2014.
Norris, G., Vedantham, R., Wade, K. S., Brown, S. G., Prouty, J. D., and Foley, C.: EPA positive matrix factorization (PMF) 3.0 fundamentals and user guide. Report by the National Exposure Research Laboratory, Sonoma Technology Inc. and Lockheed Martin Systems Engineering Center, EP-D-05-004; STI-907045.05-3347-UG, 2008.
Oltmans, S., Schnell, R., Johnson, B., Pétron, G., Mefford, T., and Neely, R.: Anatomy of wintertime ozone associated with oil and natural gas extraction activity in Wyoming and Utah, Elem. Sci. Anth., 2, 000024, https://doi.org/10.12952/journal.elementa.000024, 2014.
Paatero, P.: Least squares formulation of robust non-negative factor analysis, Chemometr. Intell. Lab., 37, 23–35, https://doi.org/10.1016/S0169-7439(96)00044-5, 1997.
Paatero, P. and Tapper, U.: Positive matrix factorization: a non-negative factor model with optimal utilization of error estimates of data values, Environmetrics, 5, 111–126, 1994.
Pétron, G., Frost, G., Miller, B. R., Hirsch, A. I., Montzka, S. A., Karion, A., Trainer, M., Sweeney, C., Andrews, A. E., Miller, L., Kofler, J., Bar-Ilan, A., Dlugokencky, E. J., Patrick, L., Moore Jr., C. T., Ryerson, T. B., Siso, C., Kolodzey, W., Lang, P. M., Conway, T., Novelli, P., Masarie, K., Hall, B., Guenther, D., Kitzis, D., Miller, J., Welsh, D., Wolfe, D., Neff, W., and Tans, P.: Hydrocarbon Emissions Characterization in the Colorado Front Range: A Pilot Study, J. Geophys. Res., 117, D04304, https://doi.org/10.1029/2011JD016360, 2012.
Poirot, R. L., Wishinski, P. R., Hopke, P. K., and Polissar, A. V.: Comparative application of multiple receptor methods to identify aerosol sources in northern Vermont, Environ. Sci. Technol., 35, 4622–4636, 2001.
Rappenglück, B., Ackermann, L., Alvarez, S., Golovko, J., Buhr, M., Field, R. A., Soltis, J., Montague, D. C., Hauze, B., Adamson, S., Risch, D., Wilkerson, G., Bush, D., Stoeckenius, T., and Keslar, C.: Strong wintertime ozone events in the Upper Green River basin, Wyoming, Atmos. Chem. Phys., 14, 4909–4934, https://doi.org/10.5194/acp-14-4909-2014, 2014.
Schauer, J. J., Kleeman, M. J., Cass, G. R., and Simoneit, B. R. T.: Measurement of emissions from air pollution sources C1 through C30 organic compounds from medium duty diesel trucks, Environ. Sci. Technol., 33, 1578–1587, 1999.
Schauer, J. J., Fraser, M. P., Cass, G. R., and Simoneit, B. R. T.: Measurement of emissions from air pollution sources C1–C32 organic compounds from gasoline-powered motor vehicles, Environ. Sci. Technol., 36, 1169–1180, 2002.
Schafer, L.: Water recycling and purification in the Pinedale Anticline Field: Results from the Anticline Disposal Project, SPE 141448, paper presented at Society of Petroleum Engineers Conference, Houston, TX, 21–23 March, 2011.
Schnell, R. C., Oltmans, S. J., Neely, R. R., Endres, M. S., Molenar, J. V., and White, A. B.: Rapid photochemical production of ozone at high concentrations in a rural site during winter, Nat. Geosci., 2, 120–122, 2009.
Soltis, J. and Field, R. A.: Upper Green River Ozone Investigation (O3i), mobile laboratory monitoring of ozone precursors at Big Piney, Luman Road, Boulder South road, Pinedale and Olson Ranch monitoring sites 2009, Report, University of Wyoming, available at: http://www-das.uwyo.edu/ozone/index.html (last access: 25 March 2015), 2009.
Soltis, J. and Field, R. A.: Pinedale Anticline Spatial Air Quality Assessment (PASQUA), mobile laboratory monitoring of ozone precursors at Boulder South Road site 2010–2011, Report, University of Wyoming, available at: http://www-das.uwyo.edu/ozone/index.html (last access: 5 August 2014), 2011a.
Soltis, J. and Field, R. A.: Pinedale Anticline Spatial Air Quality Assessment (PASQUA), 2010–2011 spatial distribution surveys, Report, University of Wyoming, available at: http://www-das.uwyo.edu/ozone/index.html (last access: 5 August 2014), 2011b.
Soltis, J. and Field, R. A.: Pinedale Anticline Spatial Air Quality Assessment (PASQUA), mobile laboratory monitoring of ozone precursors at Boulder South Road site 2011–2012, Report, University of Wyoming, available at: http://www-das.uwyo.edu/ozone/index.html (last access: 5 August 2014), 2012a.
Soltis J. and Field R.A.: Pinedale Anticline Spatial Air Quality Assessment (PASQUA), 2011–2012 spatial distribution surveys, Report, University of Wyoming, available at: http://www-das.uwyo.edu/ozone/index.html (last access: 5 August 2014), 2012b.
Song, X. H., Polissar, A. V., and Hopke, P. K.: Sources of fine particle composition in the northeastern U.S., Atmos. Environ., 35, 5277–5286, 2001.
US BLM (US Bureau of Land Management): Annual Operator Meetings, available at: http://www.blm.gov/wy/st/en/field_offices/Pinedale/anticline/airwatermtg.html (last access: 1 September 2014), 2014.
US Census Bureau: American Community Survey, US Department of Commerce, Economics and Statistics Administration, Suitland, MD, available at: http://www.census.gov/acs/www/ (last access: 24 March 2015), Report, 2010.
US Department of Energy: Modern shale gas development in the United States: A primer, Contract DE-FG26-04NT15455, 2009, Report by Office of Fossil Energy National Energy Technology Laboratory, 2009.
US EIA (US Energy Information Administration): 2009 US Crude Oil, Natural Gas and Natural Gas Liquids Proved Reserves, top100 fields, 2010, Office of Oil, Gas, and Coal Supply Statistics U.S. Department of Energy, Washington, DC 20585, available at: http://www.eia.gov/oil_gas/rpd/topfields.pdf (last access: 24 March 2015), Report, 2010.
US EIA (US Energy Information Administration): 2012 Annual energy outlook, Office of Integrated and International Energy Analysis US Department of Energy, Washington, DC 20585, available at: http://www.eia.gov/forecasts/aeo/pdf/0383(2012).pdf (last access: 24 March 2015), Report, 2012.
US EIA (US Energy Information Administration): Annual energy outlook 2014 Early Release Overview, Office of Integrated and International Energy Analysis US Department of Energy, Washington, DC 20585, available at: http://www.eia.gov/forecasts/aeo/er/pdf/0383er(2014).pdf (last access: 24 March 2015), Report, 2014.
Warneke, C., Geiger, F., Edwards, P. M., Dube, W., Pétron, G., Kofler, J., Zahn, A., Brown, S. S., Graus, M., Gilman, J. B., Lerner, B. M., Peischl, J., Ryerson, T. B., de Gouw, J. A., and Roberts, J. M.: Volatile organic compound emissions from the oil and natural gas industry in the Uintah Basin, Utah: oil and gas well pad emissions compared to ambient air composition, Atmos. Chem. Phys., 14, 10977–10988, https://doi.org/10.5194/acp-14-10977-2014, 2014.
WDEQ (Wyoming Department of Environmental Quality): Actual Emission Inventories, available at: http://deq.wyoming.gov/aqd/emission-inventories/resources/annual-and-winter-ugrb-emissions/ (last access: 4 September 2014), 2014a.
WDEQ (Wyoming Department of Environmental Quality): Wyoming Visibility Monitoring Network, available at: http://www.wyvisnet.com (last access: 4 September 2014), 2014b.
WOGCC (Wyoming Oil and Gas Conservation Commission): Gas/Water Analysis, available at: http://wogcc.state.wy.us/AnalysisMenu.cfm?Skip='Y'&oops=ID42520 (last access: 5 August 2014), 2014.
Short summary
Emissions from oil and natural gas development in the Upper Green River basin of Wyoming are known to drive wintertime ozone production. Fugitive emissions of natural gas and condensate provide sufficient non-methane hydrocarbons (NMHC) to promote episodic ozone formation. A water treatment and recycling facility was identified as a significant source of NMHC, including toluene and m+p-xylene. Emissions from this facility have a strong influence upon peak ozone measured at downwind sites.
Emissions from oil and natural gas development in the Upper Green River basin of Wyoming are...
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