Articles | Volume 15, issue 16
https://doi.org/10.5194/acp-15-9237-2015
© 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-15-9237-2015
© Author(s) 2015. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Research article
| 
20 Aug 2015
Research article |
| 20 Aug 2015
A comparison of measured HONO uptake and release with calculated source strengths in a heterogeneous forest environment
M. Sörgel
Atmospheric Chemistry, University of Bayreuth, Bayreuth, Germany
now at: Biogeochemistry Department, Max Planck Institute for Chemistry, Mainz, Germany
Environmental Research and Innovation (ERIN) Department, Luxembourg Institute of Science and Technology, Belvaux, Luxembourg
Biogeochemistry Department, Max Planck Institute for Chemistry, Mainz, Germany
A. Held
Atmospheric Chemistry, University of Bayreuth, Bayreuth, Germany
Bayreuth Center of Ecology and Environmental Research, Bayreuth, Germany
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R. Oswald, M. Ermel, K. Hens, A. Novelli, H. G. Ouwersloot, P. Paasonen, T. Petäjä, M. Sipilä, P. Keronen, J. Bäck, R. Königstedt, Z. Hosaynali Beygi, H. Fischer, B. Bohn, D. Kubistin, H. Harder, M. Martinez, J. Williams, T. Hoffmann, I. Trebs, and M. Sörgel
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Claudio Crazzolara and Andreas Held
Atmos. Meas. Tech., 17, 2183–2194, https://doi.org/10.5194/amt-17-2183-2024, https://doi.org/10.5194/amt-17-2183-2024, 2024
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Our paper describes the development of a collection device that can be used to collect airborne dust particles classified according to their size. This collection device is optimized for a special analysis method based on X-ray fluorescence so that particles can be collected from the air and analyzed with high sensitivity. This enables the determination of the content of heavy metals in the airborne particle fraction, which are of health-relevant significance.
Eike Maximilian Esders, Christoph Georgi, Wolfgang Babel, Andreas Held, and Christoph Karl Thomas
Aerosol Research Discuss., https://doi.org/10.5194/ar-2024-9, https://doi.org/10.5194/ar-2024-9, 2024
Preprint under review for AR
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Our study explores how tiny plastic particles, known as microplastics, move through the air. We focus on their journey in a wind tunnel to mimic atmospheric transport. Microplastics tend to settle closer to the ground than where they start, influenced by air speed and the height of their release. Further, this finding indicates that we can expect microplastics to accumulate in the environment, where natural dust also accumulates, offering insights for predicting their spread and impacts.
Eliane Gomes Alves, Raoni Aquino Santana, Cléo Quaresma Dias-Júnior, Santiago Botía, Tyeen Taylor, Ana Maria Yáñez-Serrano, Jürgen Kesselmeier, Efstratios Bourtsoukidis, Jonathan Williams, Pedro Ivo Lembo Silveira de Assis, Giordane Martins, Rodrigo de Souza, Sérgio Duvoisin Júnior, Alex Guenther, Dasa Gu, Anywhere Tsokankunku, Matthias Sörgel, Bruce Nelson, Davieliton Pinto, Shujiro Komiya, Diogo Martins Rosa, Bettina Weber, Cybelli Barbosa, Michelle Robin, Kenneth J. Feeley, Alvaro Duque, Viviana Londoño Lemos, Maria Paula Contreras, Alvaro Idarraga, Norberto López, Chad Husby, Brett Jestrow, and Iván Mauricio Cely Toro
Atmos. Chem. Phys., 23, 8149–8168, https://doi.org/10.5194/acp-23-8149-2023, https://doi.org/10.5194/acp-23-8149-2023, 2023
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Isoprene is emitted mainly by plants and can influence atmospheric chemistry and air quality. But, there are uncertainties in model emission estimates and follow-up atmospheric processes. In our study, with long-term observational datasets of isoprene and biological and environmental factors from central Amazonia, we show that isoprene emission estimates could be improved when biological processes were mechanistically incorporated into the model.
Jonas Elm, Aladár Czitrovszky, Andreas Held, Annele Virtanen, Astrid Kiendler-Scharr, Benjamin J. Murray, Daniel McCluskey, Daniele Contini, David Broday, Eirini Goudeli, Hilkka Timonen, Joan Rosell-Llompart, Jose L. Castillo, Evangelia Diapouli, Mar Viana, Maria E. Messing, Markku Kulmala, Naděžda Zíková, and Sebastian H. Schmitt
Aerosol Research, 1, 13–16, https://doi.org/10.5194/ar-1-13-2023, https://doi.org/10.5194/ar-1-13-2023, 2023
Janine Lückerath, Andreas Held, Holger Siebert, Michel Michalkow, and Birgit Wehner
Atmos. Chem. Phys., 22, 10007–10021, https://doi.org/10.5194/acp-22-10007-2022, https://doi.org/10.5194/acp-22-10007-2022, 2022
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Three different methods were applied to estimate the vertical aerosol particle flux in the marine boundary layer (MBL) and between the MBL and free troposphere. For the first time, aerosol fluxes derived from these three methods were estimated and compared using airborne aerosol measurements using data from the ACORES field campaign in the northeastern Atlantic Ocean in July 2017. The amount of fluxes was small and directed up and down for different cases, but the methods were applicable.
Matthias Karl, Liisa Pirjola, Tiia Grönholm, Mona Kurppa, Srinivasan Anand, Xiaole Zhang, Andreas Held, Rolf Sander, Miikka Dal Maso, David Topping, Shuai Jiang, Leena Kangas, and Jaakko Kukkonen
Geosci. Model Dev., 15, 3969–4026, https://doi.org/10.5194/gmd-15-3969-2022, https://doi.org/10.5194/gmd-15-3969-2022, 2022
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The community aerosol dynamics model MAFOR includes several advanced features: coupling with an up-to-date chemistry mechanism for volatile organic compounds, a revised Brownian coagulation kernel that takes into account the fractal geometry of soot particles, a multitude of nucleation parameterizations, size-resolved partitioning of semi-volatile inorganics, and a hybrid method for the formation of secondary organic aerosols within the framework of condensation and evaporation.
Robbie Ramsay, Chiara F. Di Marco, Mathew R. Heal, Matthias Sörgel, Paulo Artaxo, Meinrat O. Andreae, and Eiko Nemitz
Biogeosciences, 18, 2809–2825, https://doi.org/10.5194/bg-18-2809-2021, https://doi.org/10.5194/bg-18-2809-2021, 2021
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Eva Y. Pfannerstill, Nina G. Reijrink, Achim Edtbauer, Akima Ringsdorf, Nora Zannoni, Alessandro Araújo, Florian Ditas, Bruna A. Holanda, Marta O. Sá, Anywhere Tsokankunku, David Walter, Stefan Wolff, Jošt V. Lavrič, Christopher Pöhlker, Matthias Sörgel, and Jonathan Williams
Atmos. Chem. Phys., 21, 6231–6256, https://doi.org/10.5194/acp-21-6231-2021, https://doi.org/10.5194/acp-21-6231-2021, 2021
Short summary
Short summary
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Guilherme F. Camarinha-Neto, Julia C. P. Cohen, Cléo Q. Dias-Júnior, Matthias Sörgel, José Henrique Cattanio, Alessandro Araújo, Stefan Wolff, Paulo A. F. Kuhn, Rodrigo A. F. Souza, Luciana V. Rizzo, and Paulo Artaxo
Atmos. Chem. Phys., 21, 339–356, https://doi.org/10.5194/acp-21-339-2021, https://doi.org/10.5194/acp-21-339-2021, 2021
Short summary
Short summary
It was observed that friagem phenomena (incursion of cold waves from the high latitudes of the Southern Hemisphere to the Amazon region), very common in the dry season of the Amazon region, produced significant changes in microclimate and atmospheric chemistry. Moreover, the effects of the friagem change the surface O3 and CO2 mixing ratios and therefore interfere deeply in the microclimatic conditions and the chemical composition of the atmosphere above the rainforest.
Robbie Ramsay, Chiara F. Di Marco, Matthias Sörgel, Mathew R. Heal, Samara Carbone, Paulo Artaxo, Alessandro C. de Araùjo, Marta Sá, Christopher Pöhlker, Jost Lavric, Meinrat O. Andreae, and Eiko Nemitz
Atmos. Chem. Phys., 20, 15551–15584, https://doi.org/10.5194/acp-20-15551-2020, https://doi.org/10.5194/acp-20-15551-2020, 2020
Short summary
Short summary
The Amazon rainforest is a unique
laboratoryto study the processes which govern the exchange of gases and aerosols to and from the atmosphere. This study investigated these processes by measuring the atmospheric concentrations of trace gases and particles at the Amazon Tall Tower Observatory. We found that the long-range transport of pollutants can affect the atmospheric composition above the Amazon rainforest and that the gases ammonia and nitrous acid can be emitted from the rainforest.
Bruna A. Holanda, Mira L. Pöhlker, David Walter, Jorge Saturno, Matthias Sörgel, Jeannine Ditas, Florian Ditas, Christiane Schulz, Marco Aurélio Franco, Qiaoqiao Wang, Tobias Donth, Paulo Artaxo, Henrique M. J. Barbosa, Stephan Borrmann, Ramon Braga, Joel Brito, Yafang Cheng, Maximilian Dollner, Johannes W. Kaiser, Thomas Klimach, Christoph Knote, Ovid O. Krüger, Daniel Fütterer, Jošt V. Lavrič, Nan Ma, Luiz A. T. Machado, Jing Ming, Fernando G. Morais, Hauke Paulsen, Daniel Sauer, Hans Schlager, Johannes Schneider, Hang Su, Bernadett Weinzierl, Adrian Walser, Manfred Wendisch, Helmut Ziereis, Martin Zöger, Ulrich Pöschl, Meinrat O. Andreae, and Christopher Pöhlker
Atmos. Chem. Phys., 20, 4757–4785, https://doi.org/10.5194/acp-20-4757-2020, https://doi.org/10.5194/acp-20-4757-2020, 2020
Short summary
Short summary
Biomass burning smoke from African savanna and grassland is transported across the South Atlantic Ocean in defined layers within the free troposphere. The combination of in situ aircraft and ground-based measurements aided by satellite observations showed that these layers are transported into the Amazon Basin during the early dry season. The influx of aged smoke, enriched in black carbon and cloud condensation nuclei, has important implications for the Amazonian aerosol and cloud cycling.
Maurício I. Oliveira, Otávio C. Acevedo, Matthias Sörgel, Ernani L. Nascimento, Antonio O. Manzi, Pablo E. S. Oliveira, Daiane V. Brondani, Anywhere Tsokankunku, and Meinrat O. Andreae
Atmos. Chem. Phys., 20, 15–27, https://doi.org/10.5194/acp-20-15-2020, https://doi.org/10.5194/acp-20-15-2020, 2020
Short summary
Short summary
In this study, data collected during four deep convection events at the 80 m tower from the Amazon Tall Tower Observatory are analyzed. It provides a unique view on how such events affect the local boundary layer and how it recovers after their passage. Quantities analyzed include mean wind speed, virtual potential temperature, turbulent kinetic energy, sensible, and latent heat fluxes. A conceptual model for boundary layer structure along the passage of deep convection events is proposed.
Christopher Pöhlker, David Walter, Hauke Paulsen, Tobias Könemann, Emilio Rodríguez-Caballero, Daniel Moran-Zuloaga, Joel Brito, Samara Carbone, Céline Degrendele, Viviane R. Després, Florian Ditas, Bruna A. Holanda, Johannes W. Kaiser, Gerhard Lammel, Jošt V. Lavrič, Jing Ming, Daniel Pickersgill, Mira L. Pöhlker, Maria Praß, Nina Löbs, Jorge Saturno, Matthias Sörgel, Qiaoqiao Wang, Bettina Weber, Stefan Wolff, Paulo Artaxo, Ulrich Pöschl, and Meinrat O. Andreae
Atmos. Chem. Phys., 19, 8425–8470, https://doi.org/10.5194/acp-19-8425-2019, https://doi.org/10.5194/acp-19-8425-2019, 2019
Short summary
Short summary
The Amazon Tall Tower Observatory (ATTO) has been established to monitor the rain forest's biosphere–atmosphere exchange, which experiences the combined pressures from human-made deforestation and progressing climate change. This work is meant to be a reference study, which characterizes various geospatial properties of the ATTO footprint region and shows how the human-made transformation of Amazonia may impact future atmospheric observations at ATTO.
Ralph Dlugi, Martina Berger, Chinmay Mallik, Anywhere Tsokankunku, Michael Zelger, Otávio C. Acevedo, Efstratios Bourtsoukidis, Andreas Hofzumahaus, Jürgen Kesselmeier, Gerhard Kramm, Daniel Marno, Monica Martinez, Anke C. Nölscher, Huug Ouwersloot, Eva Y. Pfannerstill, Franz Rohrer, Sebastian Tauer, Jonathan Williams, Ana-Maria Yáñez-Serrano, Meinrat O. Andreae, Hartwig Harder, and Matthias Sörgel
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2018-1325, https://doi.org/10.5194/acp-2018-1325, 2019
Publication in ACP not foreseen
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Incomplete mixing (segregation) results in reduced chemical reaction rates compared to those expected from mean values and rate constants. Segregation has been suggested to cause discrepancies between modelled and measured OH radical concentrations. In this work, we summarize the intensities of segregation for the reaction of OH and isoprene for different field and modelling studies and compare those to our results from measurements in a pristine environment.
Maik Renner, Claire Brenner, Kaniska Mallick, Hans-Dieter Wizemann, Luigi Conte, Ivonne Trebs, Jianhui Wei, Volker Wulfmeyer, Karsten Schulz, and Axel Kleidon
Hydrol. Earth Syst. Sci., 23, 515–535, https://doi.org/10.5194/hess-23-515-2019, https://doi.org/10.5194/hess-23-515-2019, 2019
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We estimate the phase lag of surface states and heat fluxes to incoming solar radiation at the sub-daily timescale. While evapotranspiration reveals a minor phase lag, the vapor pressure deficit used as input by Penman–Monteith approaches shows a large phase lag. The surface-to-air temperature gradient used by energy balance residual approaches shows a small phase shift in agreement with the sensible heat flux and thus explains the better correlation of these models at the sub-daily timescale.
Robbie Ramsay, Chiara F. Di Marco, Mathew R. Heal, Marsailidh M. Twigg, Nicholas Cowan, Matthew R. Jones, Sarah R. Leeson, William J. Bloss, Louisa J. Kramer, Leigh Crilley, Matthias Sörgel, Meinrat Andreae, and Eiko Nemitz
Atmos. Chem. Phys., 18, 16953–16978, https://doi.org/10.5194/acp-18-16953-2018, https://doi.org/10.5194/acp-18-16953-2018, 2018
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Understanding the impact of agricultural activities on the atmosphere requires more measurements of inorganic trace gases and associated aerosol counterparts. This research presents 1 month of measurements above agricultural grassland during a period of fertiliser application. It was found that emissions of the important trace gases ammonia and nitrous acid peaked after fertiliser use and that the velocity at which the measured aerosols were deposited was dependent upon their size.
Barbara Altstädter, Andreas Platis, Michael Jähn, Holger Baars, Janine Lückerath, Andreas Held, Astrid Lampert, Jens Bange, Markus Hermann, and Birgit Wehner
Atmos. Chem. Phys., 18, 8249–8264, https://doi.org/10.5194/acp-18-8249-2018, https://doi.org/10.5194/acp-18-8249-2018, 2018
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This article describes the appearance of ultrafine aerosol particles (size < 12 nm) within the atmospheric boundary layer under cloudy conditions. New particle formation (NPF) was observed with the ALADINA unmanned aerial system in relation to increased turbulence near the inversion layer. Fast mixing processes and rapid dilution of surrounding air led to an insufficient particle growth rate, seen in sporadic clusters at ground. These events might not have been classified as NPF by surface data.
Pablo E. S. Oliveira, Otávio C. Acevedo, Matthias Sörgel, Anywhere Tsokankunku, Stefan Wolff, Alessandro C. Araújo, Rodrigo A. F. Souza, Marta O. Sá, Antônio O. Manzi, and Meinrat O. Andreae
Atmos. Chem. Phys., 18, 3083–3099, https://doi.org/10.5194/acp-18-3083-2018, https://doi.org/10.5194/acp-18-3083-2018, 2018
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Carbon dioxide and latent heat fluxes within the canopy are dominated by low-frequency (nonturbulent) processes. There is a striking contrast between fully turbulent and intermittent nights, such that turbulent processes dominate the total nighttime exchange during the former, while nonturbulent processes are more relevant in the latter. In very stable nights, during which intermittent exchange prevails, the stable boundary layer may be shallower than the highest observational level at 80 m.
Rüdiger Bunk, Zhigang Yi, Thomas Behrendt, Dianming Wu, Meinrat Otto Andreae, and Jürgen Kesselmeier
Biogeosciences Discuss., https://doi.org/10.5194/bg-2018-20, https://doi.org/10.5194/bg-2018-20, 2018
Manuscript not accepted for further review
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We examined the OCS exchange of four soils with the atmosphere. The laboratory setup used allowed to monitor this exchange while simultaneously monitor soil moisture. The OCS exchange of those soils was measured over full range from very wet to very dry.
We found that uptake of OCS is highly dependent on soil moisture, that probably heterotroph and autotrophs drive the uptake at different soil moistures and that the role of soils as net consumer or producers of OCS may vary with soil moisture.
Hannah Meusel, Alexandra Tamm, Uwe Kuhn, Dianming Wu, Anna Lena Leifke, Sabine Fiedler, Nina Ruckteschler, Petya Yordanova, Naama Lang-Yona, Mira Pöhlker, Jos Lelieveld, Thorsten Hoffmann, Ulrich Pöschl, Hang Su, Bettina Weber, and Yafang Cheng
Atmos. Chem. Phys., 18, 799–813, https://doi.org/10.5194/acp-18-799-2018, https://doi.org/10.5194/acp-18-799-2018, 2018
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The photolysis of nitrous acid (HONO) forms the OH radical. However, not all sources are known. Recent studies showed that HONO can be emitted from soil but they did not evaluate the importance to the HONO budget. In this work HONO emissions from 43 soil and biological soil crust samples from Cyprus were measured in a dynamic chamber and extrapolated to the real atmosphere. A large fraction of the local missing source (published earlier; Meusel et al., 2016) could be assigned to soil emissions.
Raffaella M. Vuolo, Benjamin Loubet, Nicolas Mascher, Jean-Christophe Gueudet, Brigitte Durand, Patricia Laville, Olivier Zurfluh, Raluca Ciuraru, Patrick Stella, and Ivonne Trebs
Biogeosciences, 14, 2225–2244, https://doi.org/10.5194/bg-14-2225-2017, https://doi.org/10.5194/bg-14-2225-2017, 2017
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Atmospheric nitrogen oxides (NO and NO2) are a threat for the environment and human health. Agricultural soils are a large but uncertain source, partly due to a lack of direct fluxes measurements. We quantified NO, NO2 and ozone (O3) fluxes above an oilseed rape crop rotation. We found that 0.27 % of nitrogen applied was emitted as NO, whose emissions were favoured by fertilisation under dry and warm conditions. We found significant interactions between NO, NO2 and O3 even above bare soil.
Martin Brüggemann, Laurent Poulain, Andreas Held, Torsten Stelzer, Christoph Zuth, Stefanie Richters, Anke Mutzel, Dominik van Pinxteren, Yoshiteru Iinuma, Sarmite Katkevica, René Rabe, Hartmut Herrmann, and Thorsten Hoffmann
Atmos. Chem. Phys., 17, 1453–1469, https://doi.org/10.5194/acp-17-1453-2017, https://doi.org/10.5194/acp-17-1453-2017, 2017
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Using complementary mass spectrometric techniques during a field study in central Europe, characteristic contributors to the organic aerosol mass were identified. Besides common marker compounds for biogenic secondary organic aerosol, highly oxidized sulfur species were detected in the particle phase. High-time-resolution measurements revealed correlations between these organosulfates and particulate sulfate as well as gas-phase peroxyradicals, giving hints to underlying formation mechanisms.
Kaniska Mallick, Ivonne Trebs, Eva Boegh, Laura Giustarini, Martin Schlerf, Darren T. Drewry, Lucien Hoffmann, Celso von Randow, Bart Kruijt, Alessandro Araùjo, Scott Saleska, James R. Ehleringer, Tomas F. Domingues, Jean Pierre H. B. Ometto, Antonio D. Nobre, Osvaldo Luiz Leal de Moraes, Matthew Hayek, J. William Munger, and Steven C. Wofsy
Hydrol. Earth Syst. Sci., 20, 4237–4264, https://doi.org/10.5194/hess-20-4237-2016, https://doi.org/10.5194/hess-20-4237-2016, 2016
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While quantifying vegetation water use over multiple plant function types in the Amazon Basin, we found substantial biophysical control during drought as well as a water-stress period and dominant climatic control during a water surplus period. This work has direct implication in understanding the resilience of the Amazon forest in the spectre of frequent drought menace as well as the role of drought-induced plant biophysical functioning in modulating the water-carbon coupling in this ecosystem.
Einara Zahn, Nelson L. Dias, Alessandro Araújo, Leonardo D. A. Sá, Matthias Sörgel, Ivonne Trebs, Stefan Wolff, and Antônio Manzi
Atmos. Chem. Phys., 16, 11349–11366, https://doi.org/10.5194/acp-16-11349-2016, https://doi.org/10.5194/acp-16-11349-2016, 2016
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Preliminary data from the ATTO project were analyzed to characterize the exchange of heat, water vapor, and CO2 between the Amazon forest and the atmosphere. The forest roughness makes estimation of their fluxes difficult, and even measurements at 42 m above the canopy show a lot of scatter. Still, measurements made around noon showed much better conformity with standard theories for the exchange of these quantities, opening the possibility of good flux estimates when the sun is high.
Shang Sun, Alexander Moravek, Lisa von der Heyden, Andreas Held, Matthias Sörgel, and Jürgen Kesselmeier
Atmos. Meas. Tech., 9, 599–617, https://doi.org/10.5194/amt-9-599-2016, https://doi.org/10.5194/amt-9-599-2016, 2016
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We present a dynamic twin-cuvette system for quantifying the trace gas exchange fluxes between plants and the atmosphere under controlled temperature, light, and humidity conditions. We found out that at a relative humidity of 40 %, the deposition velocity ratio of O3 and PAN was determined to be 0.45. At that humidity, the O3-deposition to the plant leaves was found to be only controlled by leaf stomata. For PAN, an additional resistance inhibited the uptake of PAN by the leaves.
M. O. Andreae, O. C. Acevedo, A. Araùjo, P. Artaxo, C. G. G. Barbosa, H. M. J. Barbosa, J. Brito, S. Carbone, X. Chi, B. B. L. Cintra, N. F. da Silva, N. L. Dias, C. Q. Dias-Júnior, F. Ditas, R. Ditz, A. F. L. Godoi, R. H. M. Godoi, M. Heimann, T. Hoffmann, J. Kesselmeier, T. Könemann, M. L. Krüger, J. V. Lavric, A. O. Manzi, A. P. Lopes, D. L. Martins, E. F. Mikhailov, D. Moran-Zuloaga, B. W. Nelson, A. C. Nölscher, D. Santos Nogueira, M. T. F. Piedade, C. Pöhlker, U. Pöschl, C. A. Quesada, L. V. Rizzo, C.-U. Ro, N. Ruckteschler, L. D. A. Sá, M. de Oliveira Sá, C. B. Sales, R. M. N. dos Santos, J. Saturno, J. Schöngart, M. Sörgel, C. M. de Souza, R. A. F. de Souza, H. Su, N. Targhetta, J. Tóta, I. Trebs, S. Trumbore, A. van Eijck, D. Walter, Z. Wang, B. Weber, J. Williams, J. Winderlich, F. Wittmann, S. Wolff, and A. M. Yáñez-Serrano
Atmos. Chem. Phys., 15, 10723–10776, https://doi.org/10.5194/acp-15-10723-2015, https://doi.org/10.5194/acp-15-10723-2015, 2015
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This paper describes the Amazon Tall Tower Observatory (ATTO), a new atmosphere-biosphere observatory located in the remote Amazon Basin. It presents results from ecosystem ecology, meteorology, trace gas, and aerosol measurements collected at the ATTO site during the first 3 years of operation.
D. Plake, M. Sörgel, P. Stella, A. Held, and I. Trebs
Biogeosciences, 12, 945–959, https://doi.org/10.5194/bg-12-945-2015, https://doi.org/10.5194/bg-12-945-2015, 2015
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Grasslands cover vast terrestrial areas and the main biomass is concentrated in the lowest part of the canopy. We found that measured transport times in the lowermost canopy layer are fastest during nighttime. During daytime, the reaction of NO with O3, as well as NO2 uptake by plants, was faster than transport. This suggests that grassland canopies of similar structure may exhibit a strong potential to retain soil emitted NO due to oxidation and subsequent uptake of NO2 by plants.
A. Moravek, P. Stella, T. Foken, and I. Trebs
Atmos. Chem. Phys., 15, 899–911, https://doi.org/10.5194/acp-15-899-2015, https://doi.org/10.5194/acp-15-899-2015, 2015
R. Oswald, M. Ermel, K. Hens, A. Novelli, H. G. Ouwersloot, P. Paasonen, T. Petäjä, M. Sipilä, P. Keronen, J. Bäck, R. Königstedt, Z. Hosaynali Beygi, H. Fischer, B. Bohn, D. Kubistin, H. Harder, M. Martinez, J. Williams, T. Hoffmann, I. Trebs, and M. Sörgel
Atmos. Chem. Phys., 15, 799–813, https://doi.org/10.5194/acp-15-799-2015, https://doi.org/10.5194/acp-15-799-2015, 2015
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Nitrous acid (HONO) is a key species in atmospheric photochemistry since the photolysis leads to the important hydroxyl radical (OH). Although the importance of HONO as a precursor of OH is known, the formation pathways of HONO, especially during daytime, are a major challenge in atmospheric science. We present a detailed analysis of sources and sinks for HONO in the atmosphere for a field measurement campaign in the boreal forest in Finland and wonder if there is really a source term missing.
S. G. Gonser, F. Klein, W. Birmili, J. Größ, M. Kulmala, H. E. Manninen, A. Wiedensohler, and A. Held
Atmos. Chem. Phys., 14, 10547–10563, https://doi.org/10.5194/acp-14-10547-2014, https://doi.org/10.5194/acp-14-10547-2014, 2014
A. Moravek, T. Foken, and I. Trebs
Atmos. Meas. Tech., 7, 2097–2119, https://doi.org/10.5194/amt-7-2097-2014, https://doi.org/10.5194/amt-7-2097-2014, 2014
M. Tjernström, C. Leck, C. E. Birch, J. W. Bottenheim, B. J. Brooks, I. M. Brooks, L. Bäcklin, R. Y.-W. Chang, G. de Leeuw, L. Di Liberto, S. de la Rosa, E. Granath, M. Graus, A. Hansel, J. Heintzenberg, A. Held, A. Hind, P. Johnston, J. Knulst, M. Martin, P. A. Matrai, T. Mauritsen, M. Müller, S. J. Norris, M. V. Orellana, D. A. Orsini, J. Paatero, P. O. G. Persson, Q. Gao, C. Rauschenberg, Z. Ristovski, J. Sedlar, M. D. Shupe, B. Sierau, A. Sirevaag, S. Sjogren, O. Stetzer, E. Swietlicki, M. Szczodrak, P. Vaattovaara, N. Wahlberg, M. Westberg, and C. R. Wheeler
Atmos. Chem. Phys., 14, 2823–2869, https://doi.org/10.5194/acp-14-2823-2014, https://doi.org/10.5194/acp-14-2823-2014, 2014
N. Niedermeier, A. Held, T. Müller, B. Heinold, K. Schepanski, I. Tegen, K. Kandler, M. Ebert, S. Weinbruch, K. Read, J. Lee, K. W. Fomba, K. Müller, H. Herrmann, and A. Wiedensohler
Atmos. Chem. Phys., 14, 2245–2266, https://doi.org/10.5194/acp-14-2245-2014, https://doi.org/10.5194/acp-14-2245-2014, 2014
K. A. Kamilli, L. Poulain, A. Held, A. Nowak, W. Birmili, and A. Wiedensohler
Atmos. Chem. Phys., 14, 737–749, https://doi.org/10.5194/acp-14-737-2014, https://doi.org/10.5194/acp-14-737-2014, 2014
P. Stella, M. Kortner, C. Ammann, T. Foken, F. X. Meixner, and I. Trebs
Biogeosciences, 10, 5997–6017, https://doi.org/10.5194/bg-10-5997-2013, https://doi.org/10.5194/bg-10-5997-2013, 2013
S. G. Gonser and A. Held
Atmos. Meas. Tech., 6, 2339–2348, https://doi.org/10.5194/amt-6-2339-2013, https://doi.org/10.5194/amt-6-2339-2013, 2013
D. Plake and I. Trebs
Atmos. Meas. Tech., 6, 1017–1030, https://doi.org/10.5194/amt-6-1017-2013, https://doi.org/10.5194/amt-6-1017-2013, 2013
Related subject area
Subject: Gases | Research Activity: Field Measurements | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Contribution of cooking emissions to the urban volatile organic compounds in Las Vegas, NV
Reanalysis of NOAA H2 observations: implications for the H2 budget
A large role of missing volatile organic compound reactivity from anthropogenic emissions in ozone pollution regulation
Measurement report: Insights into the chemical composition and origin of molecular clusters and potential precursor molecules present in the free troposphere over the southern Indian Ocean: observations from the Maïdo Observatory (2150 m a.s.l., Réunion)
Production of oxygenated volatile organic compounds from the ozonolysis of coastal seawater
Comment on “Transport of substantial stratospheric ozone to the surface by a dying typhoon and shallow convection” by Chen et al. (2022)
Observations of cyanogen bromide (BrCN) in the global troposphere and their relation to polar surface O3 destruction
Individual coal mine methane emissions constrained by eddy covariance measurements: low bias and missing sources
Measurement report: Observations of ground-level ozone concentration gradients perpendicular to the Lake Ontario shoreline
Measurement report: The Palau Atmospheric Observatory and its ozonesonde record – continuous monitoring of tropospheric composition and dynamics in the tropical western Pacific
Quantifying SO2 oxidation pathways to atmospheric sulfate using stable sulfur and oxygen isotopes: laboratory simulation and field observation
Influences of downward transport and photochemistry on surface ozone over East Antarctica during austral summer: in situ observations and model simulations
Iodine oxoacids and their roles in sub-3 nm particle growth in polluted urban environments
Intensive photochemical oxidation in the marine atmosphere: evidence from direct radical measurements
Diurnal variations in oxygen and nitrogen isotopes of atmospheric nitrogen dioxide and nitrate: implications for tracing NOx oxidation pathways and emission sources
Measurement report: Method for evaluating CO2 emissions from a cement plant using atmospheric δ(O2 ∕ N2) and CO2 measurements and its implication for future detection of CO2 capture signals
Aircraft-based mass balance estimate of methane emissions from offshore gas facilities in the southern North Sea
Parameterizations of US wildfire and prescribed fire emission ratios and emission factors based on FIREX-AQ aircraft measurements
Measurement report: Atmospheric nitrate radical chemistry in the South China Sea influenced by the urban outflow of the Pearl River Delta
The interhemispheric gradient of SF6 in the upper troposphere
Weather regimes and the related atmospheric composition at a Pyrenean observatory characterized by hierarchical clustering of a 5-year data set
Tropospheric bromine monoxide vertical profiles retrieved across the Alaskan Arctic in springtime
Source apportionment of methane emissions from the Upper Silesian Coal Basin using isotopic signatures
Measurement report: Exchange fluxes of HONO over agricultural fields in the North China Plain
HONO chemistry at a suburban site during the EXPLORE-YRD campaign in 2018: formation mechanisms and impacts on O3 production
Evaluation of modelled climatologies of O3, CO, water vapour and NOy in the upper troposphere–lower stratosphere using regular in situ observations by passenger aircraft
Photochemical ageing of aerosols contributes significantly to the production of atmospheric formic acid
Nitrous acid budgets in the coastal atmosphere: potential daytime marine sources
Sources of organic gases and aerosol particles and their roles in nighttime particle growth at a rural forested site in southwest Germany
Undetected biogenic volatile organic compounds from Norway spruce drive total ozone reactivity measurements
Quantification of fossil fuel CO2 from combined CO, δ13CO2 and Δ14CO2 observations
Radical chemistry and ozone production at a UK coastal receptor site
Sources and long-term variability of carbon monoxide at Mount Kenya and in Nairobi
Shipping and algae emissions have a major impact on ambient air mixing ratios of NMHCs and methanethiol on Utö island in the Baltic Sea
Opinion: Strengthening Research in the Global South: Atmospheric Science Opportunities in South America and Africa
Measurement report: Airborne measurements of NOx fluxes over Los Angeles during the RECAP-CA 2021 campaign
Influence of anthropogenic emissions on the composition of highly oxygenated organic molecules in Helsinki: a street canyon and urban background station comparison
Changes in surface ozone in South Korea on diurnal to decadal timescales for the period of 2001–2021
Characterization of the nitrogen stable isotope composition (δ15N) of ship-emitted NOx
Volatile organic compound fluxes in the agricultural San Joaquin Valley – spatial distribution, source attribution, and inventory comparison
Exploring the amplified role of HCHO in the formation of HMS and O3 during the co-occurring PM2.5 and O3 pollution in a coastal city of southeast China
High potential for CH4 emission mitigation from oil infrastructure in one of EU's major production regions
Measurement report: Source apportionment and environmental impacts of volatile organic compounds (VOCs) in Lhasa, a highland city in China
OH, HO2, and RO2 radical chemistry in a rural forest environment: measurements, model comparisons, and evidence of a missing radical sink
The atmospheric fate of 1,2-dibromo-4-(1,2-dibromoethyl)cyclohexane (TBECH): spatial patterns, seasonal variability, and deposition to Canadian coastal regions
A single-point modeling approach for the intercomparison and evaluation of ozone dry deposition across chemical transport models (Activity 2 of AQMEII4)
Direct observations of NOx emissions over the San Joaquin Valley using airborne flux measurements during RECAP-CA 2021 field campaign
Surface snow bromide and nitrate at Eureka, Canada in early spring and implications for polar boundary layer chemistry
Trends and seasonal variability in ammonia across major biomes in western and central Africa inferred from long-term series of ground-based and satellite measurements
A rise in HFC-23 emissions from eastern Asia since 2015
Matthew M. Coggon, Chelsea E. Stockwell, Lu Xu, Jeff Peischl, Jessica B. Gilman, Aaron Lamplugh, Henry J. Bowman, Kenneth Aikin, Colin Harkins, Qindan Zhu, Rebecca H. Schwantes, Jian He, Meng Li, Karl Seltzer, Brian McDonald, and Carsten Warneke
Atmos. Chem. Phys., 24, 4289–4304, https://doi.org/10.5194/acp-24-4289-2024, https://doi.org/10.5194/acp-24-4289-2024, 2024
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Residential and commercial cooking emits pollutants that degrade air quality. Here, ambient observations show that cooking is an important contributor to anthropogenic volatile organic compounds (VOCs) emitted in Las Vegas, NV. These emissions are not fully presented in air quality models, and more work may be needed to quantify emissions from important sources, such as commercial restaurants.
Fabien Paulot, Gabrielle Pétron, Andrew M. Crotwell, and Matteo B. Bertagni
Atmos. Chem. Phys., 24, 4217–4229, https://doi.org/10.5194/acp-24-4217-2024, https://doi.org/10.5194/acp-24-4217-2024, 2024
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New data from the National Oceanic and Atmospheric Administration show that hydrogen (H2) concentrations increased from 2010 to 2019, which is consistent with the simulated increase in H2 photochemical production (mainly from methane). But this cannot be reconciled with the expected decrease (increase) in H2 anthropogenic emissions (soil deposition) in the same period. This shows gaps in our knowledge of the H2 biogeochemical cycle that must be resolved to quantify the impact of higher H2 usage.
Wenjie Wang, Bin Yuan, Hang Su, Yafang Cheng, Jipeng Qi, Sihang Wang, Wei Song, Xinming Wang, Chaoyang Xue, Chaoqun Ma, Fengxia Bao, Hongli Wang, Shengrong Lou, and Min Shao
Atmos. Chem. Phys., 24, 4017–4027, https://doi.org/10.5194/acp-24-4017-2024, https://doi.org/10.5194/acp-24-4017-2024, 2024
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This study investigates the important role of unmeasured volatile organic compounds (VOCs) in ozone formation. Based on results in a megacity of China, we show that unmeasured VOCs can contribute significantly to ozone fomation and also influence the determination of ozone control strategy. Our results show that these unmeasured VOCs are mainly from human sources.
Romain Salignat, Matti Rissanen, Siddharth Iyer, Jean-Luc Baray, Pierre Tulet, Jean-Marc Metzger, Jérôme Brioude, Karine Sellegri, and Clémence Rose
Atmos. Chem. Phys., 24, 3785–3812, https://doi.org/10.5194/acp-24-3785-2024, https://doi.org/10.5194/acp-24-3785-2024, 2024
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Using mass spectrometry data collected at the Maïdo Observatory (2160 m a.s.l., Réunion), we provide the first detailed analysis of molecular cluster chemical composition specifically in the marine free troposphere. The abundance of the identified species is related both to in situ meteorological parameters and air mass history, which also provide insight into their origin. Our work makes an important contribution to documenting the chemistry and physics of the marine free troposphere.
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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Laboratory experiments with seawater mimics suggest ozone deposition to the surface ocean can be a source of reactive carbon to the marine atmosphere. We conduct both field and laboratory measurements to assess abiotic VOC composition and yields from ozonolysis of real surface seawater. We show that C5–C11 aldehydes contribute to the observed VOC emission flux. We estimate that VOCs generated by the ozonolysis of surface seawater are competitive with biological VOC production and emission.
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.
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.
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.
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.
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.
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.
Junwei Song, Harald Saathoff, Feng Jiang, Linyu Gao, Hengheng Zhang, and Thomas Leisner
EGUsphere, https://doi.org/10.5194/egusphere-2023-2255, https://doi.org/10.5194/egusphere-2023-2255, 2023
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This study presents the concurrent online measurements of organic gas and particles (VOCs and OA) at a forest site in summer. Both VOCs and OA were largely contributed by oxygenated organic compounds. Semi-volatile oxygenated OA and organic nitrate formed from monoterpenes and sesquiterpenes contribute significantly to nighttime particle growth. The results help to understand the causes of nighttime particle growth regularly observed in summer in the central European rural forested environments.
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.
Heidi Hellén, Rostislav Kouznetsov, Kaisa Kraft, Jukka Seppälä, Mika Vestenius, Jukka-Pekka Jalkanen, Lauri Laakso, and Hannele Hakola
EGUsphere, https://doi.org/10.5194/egusphere-2023-2323, https://doi.org/10.5194/egusphere-2023-2323, 2023
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Mixing ratios of C2-C5 NMHCs and methanethiol were measured on an island in Baltic Sea using an in-situ gas chromatograph. Shipping emissions were found to be an important source of ethene, ethyne, propene and benzene. High summertime mixing ratios of methanethiol and dependence of mixing ratios on sea water temperature and height indicated the biogenic origin possibly from phytoplankton or macroalgae. These emissions may have strong impacts on SO2 production and new particle formation.
Rebecca M. Garland, Katye E. Altieri, Laura Dawidowski, Laura Gallardo, Aderiana Mbandi, Nestor Y. Rojas, and N'datchoh E. Touré
EGUsphere, https://doi.org/10.5194/egusphere-2023-2566, https://doi.org/10.5194/egusphere-2023-2566, 2023
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In this opinion, we focus on two geographical areas in the Global South to discuss some common challenges and constraints, with a focus on our strengths in atmospheric science research. It is these strengths, we believe, that highlight the critical role of Global South researchers in the future of atmospheric science research.
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.
Magdalena Okuljar, Olga Garmash, Miska Olin, Joni Kalliokoski, Hilkka Timonen, Jarkko V. Niemi, Pauli Paasonen, Jenni Kontkanen, Yanjun Zhang, Heidi Hellén, Heino Kuuluvainen, Minna Aurela, Hanna E. Manninen, Mikko Sipilä, Topi Rönkkö, Tuukka Petäjä, Markku Kulmala, Miikka Dal Maso, and Mikael Ehn
Atmos. Chem. Phys., 23, 12965–12983, https://doi.org/10.5194/acp-23-12965-2023, https://doi.org/10.5194/acp-23-12965-2023, 2023
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Highly oxygenated organic molecules (HOMs) form secondary organic aerosol that affects air quality and health. In this study, we demonstrate that in a moderately polluted city with abundant vegetation, the composition of HOMs is largely controlled by the effect of NOx on the biogenic volatile organic compound oxidation. Comparing the results from two nearby stations, we show that HOM composition and formation pathways can change considerably within small distances in urban environments.
Si-Wan Kim, Kyoung-Min Kim, Yujoo Jeong, Seunghwan Seo, Yeonsu Park, and Jeongyeon Kim
Atmos. Chem. Phys., 23, 12867–12886, https://doi.org/10.5194/acp-23-12867-2023, https://doi.org/10.5194/acp-23-12867-2023, 2023
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Surface ozone is a pollutant regulated for public health. This study derived surface ozone trends over South Korea from 2001 to 2021 and highlighted that South Korea has been a nonattainment area since 2010, based on the US EPA standard. However, the occurrences of high ozone condition decreased in spring during the COVID-19 pandemic, partly due to large reductions of ozone precursor concentrations in China and South Korea.
Zeyu Sun, Zheng Zong, Yang Tan, Chongguo Tian, Zeyu Liu, Fan Zhang, Rong Sun, Yingjun Chen, Jun Li, and Gan Zhang
Atmos. Chem. Phys., 23, 12851–12865, https://doi.org/10.5194/acp-23-12851-2023, https://doi.org/10.5194/acp-23-12851-2023, 2023
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This is the first report of ship-emitted nitrogen stable isotope composition (δ15N) of nitrogen oxides (NOx). The results showed that δ15N–NOx from ships was −18.5 ± 10.9 ‰ and increased monotonically with tightening emission regulations. The selective catalytic reduction system was the most vital factor. The temporal variation in δ15N–NOx was evaluated and can be used to select suitable δ15N–NOx for a more accurate assessment of the contribution of ship-emitted exhaust to atmospheric NOx.
Eva Y. Pfannerstill, Caleb Arata, Qindan Zhu, Benjamin C. Schulze, Roy Woods, John H. Seinfeld, Anthony Bucholtz, Ronald C. Cohen, and Allen H. Goldstein
Atmos. Chem. Phys., 23, 12753–12780, https://doi.org/10.5194/acp-23-12753-2023, https://doi.org/10.5194/acp-23-12753-2023, 2023
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The San Joaquin Valley is an agricultural area with poor air quality. Organic gases drive the formation of hazardous air pollutants. Agricultural emissions of these gases are not well understood and have rarely been quantified at landscape scale. By combining aircraft-based emission measurements with land cover information, we found mis- or unrepresented emission sources. Our results help in understanding of pollution sources and in improving predictions of air quality in agricultural regions.
Youwei Hong, Keran Zhang, Dan Liao, Gaojie Chen, Min Zhao, Yiling Lin, Xiaoting Ji, Ke Xu, Yu Wu, Ruilian Yu, Gongren Hu, Sung-Deuk Choi, Likun Xue, and Jinsheng Chen
Atmos. Chem. Phys., 23, 10795–10807, https://doi.org/10.5194/acp-23-10795-2023, https://doi.org/10.5194/acp-23-10795-2023, 2023
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Particle uptakes of HCHO and the impacts on PM2.5 and O3 production remain highly uncertain. Based on the investigation of co-occurring wintertime O3 and PM2.5 pollution in a coastal city of southeast China, we found enhanced heterogeneous formation of hydroxymethanesulfonate (HMS) and increased ROx concentrations and net O3 production rates. The findings of this study are helpful to better explore the mechanisms of key precursors for co-occurring PM2.5 and O3 pollution.
Foteini Stavropoulou, Katarina Vinković, Bert Kers, Marcel de Vries, Steven van Heuven, Piotr Korbeń, Martina Schmidt, Julia Wietzel, Pawel Jagoda, Jaroslav M. Necki, Jakub Bartyzel, Hossein Maazallahi, Malika Menoud, Carina van der Veen, Sylvia Walter, Béla Tuzson, Jonas Ravelid, Randulph Paulo Morales, Lukas Emmenegger, Dominik Brunner, Michael Steiner, Arjan Hensen, Ilona Velzeboer, Pim van den Bulk, Hugo Denier van der Gon, Antonio Delre, Maklawe Essonanawe Edjabou, Charlotte Scheutz, Marius Corbu, Sebastian Iancu, Denisa Moaca, Alin Scarlat, Alexandru Tudor, Ioana Vizireanu, Andreea Calcan, Magdalena Ardelean, Sorin Ghemulet, Alexandru Pana, Aurel Constantinescu, Lucian Cusa, Alexandru Nica, Calin Baciu, Cristian Pop, Andrei Radovici, Alexandru Mereuta, Horatiu Stefanie, Alexandru Dandocsi, Bas Hermans, Stefan Schwietzke, Daniel Zavala-Araiza, Huilin Chen, and Thomas Röckmann
Atmos. Chem. Phys., 23, 10399–10412, https://doi.org/10.5194/acp-23-10399-2023, https://doi.org/10.5194/acp-23-10399-2023, 2023
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In this study, we quantify CH4 emissions from onshore oil production sites in Romania at source and facility level using a combination of ground- and drone-based measurement techniques. We show that the total CH4 emissions in our studied areas are much higher than the emissions reported to UNFCCC, and up to three-quarters of the detected emissions are related to operational venting. Our results suggest that oil and gas production infrastructure in Romania holds a massive mitigation potential.
Chunxiang Ye, Shuzheng Guo, Weili Lin, Fangjie Tian, Jianshu Wang, Chong Zhang, Suzhen Chi, Yi Chen, Yingjie Zhang, Limin Zeng, Xin Li, Duo Bu, Jiacheng Zhou, and Weixiong Zhao
Atmos. Chem. Phys., 23, 10383–10397, https://doi.org/10.5194/acp-23-10383-2023, https://doi.org/10.5194/acp-23-10383-2023, 2023
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Online volatile organic compound (VOC) measurements by gas chromatography–mass spectrometry, with other O3 precursors, were used to identify key VOC and other key sources in Lhasa. Total VOCs (TVOCs), alkanes, and aromatics are half as abundant as in Beijing. Oxygenated VOCs (OVOCs) consist of 52 % of the TVOCs. Alkenes and OVOCs account for 80 % of the ozone formation potential. Aromatics dominate secondary organic aerosol potential. Positive matrix factorization decomposed residential sources.
Brandon Bottorff, Michelle M. Lew, Youngjun Woo, Pamela Rickly, Matthew D. Rollings, Benjamin Deming, Daniel C. Anderson, Ezra Wood, Hariprasad D. Alwe, Dylan B. Millet, Andrew Weinheimer, Geoff Tyndall, John Ortega, Sebastien Dusanter, Thierry Leonardis, James Flynn, Matt Erickson, Sergio Alvarez, Jean C. Rivera-Rios, Joshua D. Shutter, Frank Keutsch, Detlev Helmig, Wei Wang, Hannah M. Allen, Johnathan H. Slade, Paul B. Shepson, Steven Bertman, and Philip S. Stevens
Atmos. Chem. Phys., 23, 10287–10311, https://doi.org/10.5194/acp-23-10287-2023, https://doi.org/10.5194/acp-23-10287-2023, 2023
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The hydroxyl (OH), hydroperoxy (HO2), and organic peroxy (RO2) radicals play important roles in atmospheric chemistry and have significant air quality implications. Here, we compare measurements of OH, HO2, and total peroxy radicals (XO2) made in a remote forest in Michigan, USA, to predictions from a series of chemical models. Lower measured radical concentrations suggest that the models may be missing an important radical sink and overestimating the rate of ozone production in this forest.
Jenny Oh, Chubashini Shunthirasingham, Ying Duan Lei, Faqiang Zhan, Yuening Li, Abigaëlle Dalpé Castilloux, Amina Ben Chaaben, Zhe Lu, Kelsey Lee, Frank A. P. C. Gobas, Sabine Eckhardt, Nick Alexandrou, Hayley Hung, and Frank Wania
Atmos. Chem. Phys., 23, 10191–10205, https://doi.org/10.5194/acp-23-10191-2023, https://doi.org/10.5194/acp-23-10191-2023, 2023
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An emerging brominated flame retardant (BFR) called TBECH (1,2-dibromo-4-(1,2-dibromoethyl)cyclohexane) has never been produced or imported for use in Canada yet is found to be one of the most abundant gaseous BFRs in the Canadian atmosphere. The recorded spatial and temporal variability of TBECH suggest that the release from imported consumer products containing TBECH is the most likely explanation for its environmental occurrence in Canada.
Olivia E. Clifton, Donna Schwede, Christian Hogrefe, Jesse O. Bash, Sam Bland, Philip Cheung, Mhairi Coyle, Lisa Emberson, Johannes Flemming, Erick Fredj, Stefano Galmarini, Laurens Ganzeveld, Orestis Gazetas, Ignacio Goded, Christopher D. Holmes, László Horváth, Vincent Huijnen, Qian Li, Paul A. Makar, Ivan Mammarella, Giovanni Manca, J. William Munger, Juan L. Pérez-Camanyo, Jonathan Pleim, Limei Ran, Roberto San Jose, Sam J. Silva, Ralf Staebler, Shihan Sun, Amos P. K. Tai, Eran Tas, Timo Vesala, Tamás Weidinger, Zhiyong Wu, and Leiming Zhang
Atmos. Chem. Phys., 23, 9911–9961, https://doi.org/10.5194/acp-23-9911-2023, https://doi.org/10.5194/acp-23-9911-2023, 2023
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A primary sink of air pollutants is dry deposition. Dry deposition estimates differ across the models used to simulate atmospheric chemistry. Here, we introduce an effort to examine dry deposition schemes from atmospheric chemistry models. We provide our approach’s rationale, document the schemes, and describe datasets used to drive and evaluate the schemes. We also launch the analysis of results by evaluating against observations and identifying the processes leading to model–model differences.
Qindan Zhu, Bryan Place, Eva Y. Pfannerstill, Sha Tong, Huanxin Zhang, Jun Wang, Clara M. Nussbaumer, Paul Wooldridge, Benjamin C. Schulze, Caleb Arata, Anthony Bucholtz, John H. Seinfeld, Allen H. Goldstein, and Ronald C. Cohen
Atmos. Chem. Phys., 23, 9669–9683, https://doi.org/10.5194/acp-23-9669-2023, https://doi.org/10.5194/acp-23-9669-2023, 2023
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Nitrogen oxide (NOx) is a hazardous air pollutant, and it is the precursor of short-lived climate forcers like tropospheric ozone and aerosol particles. While NOx emissions from transportation has been strictly regulated, soil NOx emissions are overlooked. We use the airborne flux measurements to observe NOx emissions from highways and urban and cultivated soil land cover types. We show non-negligible soil NOx emissions, which are significantly underestimated in current model simulations.
Xin Yang, Kimberly Strong, Alison Criscitiello, Marta Santos-Garcia, Kristof Bognar, Xiaoyi Zhao, Pierre Fogal, Kaley Walker, Sara Morris, and Peter Effertz
EGUsphere, https://doi.org/10.5194/egusphere-2023-1446, https://doi.org/10.5194/egusphere-2023-1446, 2023
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This study uses in-situ field data collected from a Canadian high Arctic site to demonstrate that surface snow in early spring is a net sink of atmospheric bromine and nitrogen. In addition, surface snow bromide and nitrate are significantly correlated, one molecule bromide deposited is accompanied by 4–7 molecules nitrate, indicating the oxidation of reactive nitrogen is accelerated by reactive bromine. This is the first time such an effect was seen in snow chemistry on a time scale of one day.
Money Ossohou, Jonathan Edward Hickman, Lieven Clarisse, Pierre-François Coheur, Martin Van Damme, Marcellin Adon, Véronique Yoboué, Eric Gardrat, Maria Dias Alvès, and Corinne Galy-Lacaux
Atmos. Chem. Phys., 23, 9473–9494, https://doi.org/10.5194/acp-23-9473-2023, https://doi.org/10.5194/acp-23-9473-2023, 2023
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The updated analyses of ground-based concentrations and satellite total vertical columns of atmospheric ammonia help us to better understand 21st century ammonia dynamics in sub-Saharan Africa. We conclude that the drivers of trends are agriculture in the dry savanna of Katibougou, Mali; air temperature and agriculture in the wet savanna of Djougou, Benin, and Lamto, Côte d'Ivoire; and leaf area index, air temperature, residential, and agriculture in forests of Bomassa, Republic of Congo.
Hyeri Park, Jooil Kim, Haklim Choi, Sohyeon Geum, Yeaseul Kim, Rona L. Thompson, Jens Mühle, Peter K. Salameh, Christina M. Harth, Kieran M. Stanley, Simon O'Doherty, Paul J. Fraser, Peter G. Simmonds, Paul B. Krummel, Ray F. Weiss, Ronald G. Prinn, and Sunyoung Park
Atmos. Chem. Phys., 23, 9401–9411, https://doi.org/10.5194/acp-23-9401-2023, https://doi.org/10.5194/acp-23-9401-2023, 2023
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Based on atmospheric HFC-23 observations, the first estimate of post-CDM HFC-23 emissions in eastern Asia for 2008–2019 shows that these emissions contribute significantly to the global emissions rise. The observation-derived emissions were much larger than the bottom-up estimates expected to approach zero after 2015 due to national abatement activities. These discrepancies could be attributed to unsuccessful factory-level HFC-23 abatement and inaccurate quantification of emission reductions.
Cited articles
Abida, O., Du, J., and Zhu, L.: Investigation of the photolysis of the surface-adsorbed HNO3 by combining laser photolysis with Brewster angle cavity ring-down spectroscopy, Chem. Phys. Lett., 534, 77–82, 2012.
Alicke, B., Geyer, A., Hofzumahaus, A., Holland, F., Konrad, S., Pätz, H. W., Schäfer, J., Stutz, J., Volz-Thomas, A., and Platt, U.: OH formation by HONO photolysis during the BERLIOZ experiment, J. Geophys. Res., 108, 8247, https://doi.org/10.1029/2001JD000579, 2003.
Allison, F.: Losses of gaseous nitrogen from soils by chemical mechanisms involving nitrous acid and nitrites, Soil Sci., 96, 404–409, 1963.
Amedro, D., Parker, A. E., Schoemaecker, C., and Fittschen, C.: Direct observation of OH radicals after 565 nm multi-photon excitation of NO2 in the presence of H2O, Chem. Phys. Lett., 513, 12–16, 2011.
Arens, F., Gutzwiller, L., Baltensperger, U. R., Gäggler, H. W., and Ammann, M.: Heterogeneous reaction of NO2 on diesel soot particles, Environ. Sci. Technol., 35, 2191–2199, 2001.
Aubin, D. G. and Abbatt, J. P. D.: Interaction of NO2 with hydrocarbon soot: focus on HONO yield, surface modification, and mechanism, J. Phys. Chem. A, 111, 6263–6273, 2007.
Bargsten, A., Falge, E., Pritsch, K., Huwe, B., and Meixner, F. X.: Laboratory measurements of nitric oxide release from forest soil with a thick organic layer under different understory types, Biogeosciences, 7, 1425–1441, https://doi.org/10.5194/bg-7-1425-2010, 2010.
Bartels-Rausch, T., Brigante, M., Elshorbany, Y. F., Ammann, M., D'Anna, B., George, C., Stemmler, K., Ndour, M., and Kleffmann, J.: Humic acid in ice: Photo-enhanced conversion of nitrogen dioxide into nitrous acid, Atmos. Environ., 44, 5443–5450, 2010.
Bejan, I., Aal, Y. A. E., Barnes, I., Benter, T., Bohn, B., Wiesen, P., and Kleffmann, J.: The photolysis of ortho-nitrophenols: a new gas phase source of HONO, Phys. Chem. Chem. Phys., 8, 2028–2035, https://doi.org/10.1039/b516590c, 2006.
Clark, F. E.: Losses of nitrogen accompanying nitrification, Transactions of the International Society of Soil Science, Communications IV and V, Lower Hutt, New Zealand, 173–176, 1962.
Colussi, A. J., Enami, S., Yabushita, A., Hoffmann, M. R., Liu, W.-G., Mishraaf, H., and Goddard, W. A.: Tropospheric aerosol as a reactive intermediate, Faraday Discuss., 165, 407–420, 2013.
Cox, R. A.: The photolysis of nitrous acid in the presence of carbon monoxide and sulphur dioxide, J. Photochem., 3, 291–304, 1974.
Crowley, J. N. and Carl, S. A.: OH formation in the photoexcitation of NO2 beyond the dissociation threshold in the presence of water vapor, J. Phys. Chem. A, 101, 4178–4184, 1997.
Czader, B. H., Rappenglück, B., Percell, P., Byun, D. W., Ngan, F., and Kim, S.: Modeling nitrous acid and its impact on ozone and hydroxyl radical during the Texas Air Quality Study 2006, Atmos. Chem. Phys., 12, 6939–6951, https://doi.org/10.5194/acp-12-6939-2012, 2012.
De Boer, W. and Kowalchuk, G. A.: Nitrification in acid soils: micro-organisms and mechanisms, Soil Biol. Biochem., 33, 853–866, 2001.
De Jesus Medeiros, D. and Pimentel, A. S.: New insights in the atmospheric HONO formation: New pathways for N2O4 isomerization and NO2 dimerization in the presence of water, J. Phys. Chem. A, 115, 6357–6365, 2011.
Donaldson, M. A., Berke, A. E., and Raff, J. D.: Uptake of Gas Phase Nitrous Acid onto Boundary Layer Soil Surfaces, Environ. Sci. Technol., 48, 375–383, https://doi.org/10.1021/es404156a, 2014a.
Donaldson, M. A., Bish, D. L., and Raff, J. D.: Soil surface acidity plays a determining role in the atmospheric-terrestrial exchange of nitrous acid, P. Natl. Acad. Sci. USA, 111, 18472–18477, https://doi.org/10.1073/pnas.1418545112, 2014b.
Febo, A., Perrino, C., and Allegrini, I.: Measurement of nitrous acid in Milan, Italy, by DOAS and diffusion denuders, Atmos. Environ., 30 3599–3609, 1996.
Finlayson-Pitts, B. J.: Reactions at surfaces in the atmosphere: integration of experiments and theory as necessary (but not necessarily sufficient) for predicting the physical chemistry of aerosols, Phys. Chem. Chem. Phys., 11, 7760–7779, 2009.
Finlayson-Pitts, B. J., Wingen, L. M., Sumner, A. L., Syomin, D., and Ramazan, K. A.: The heterogeneous hydrolysis of NO2 in laboratory systems and in outdoor and indoor atmospheres: An integrated mechanism, Phys. Chem. Chem. Phys., 5, 223–242, 2003.
Foken, T.: Lufthygienisch-bioklimatische Kennzeichnung des oberen Egertales (Fichtelgebirge bis Karlovy Vary), Bayreuther Forum Ökologie, 100, Bayreuth, Germany, 70 pp., 2003.
Foken, T: Micrometeorology, Springer, Heidelberg, Germany, 308 pp., 2008.
Foken, T., Meixner, F. X., Falge, E., Zetzsch, C., Serafimovich, A., Bargsten, A., Behrendt, T., Biermann, T., Breuninger, C., Dix, S., Gerken, T., Hunner, M., Lehmann-Pape, L., Hens, K., Jocher, G., Kesselmeier, J., Lüers, J., Mayer, J.-C., Moravek, A., Plake, D., Riederer, M., Rütz, F., Scheibe, M., Siebicke, L., Sörgel, M., Staudt, K., Trebs, I., Tsokankunku, A., Welling, M., Wolff, V., and Zhu, Z.: Coupling processes and exchange of energy and reactive and non-reactive trace gases at a forest site – results of the EGER experiment, Atmos. Chem. Phys., 12, 1923–1950, https://doi.org/10.5194/acp-12-1923-2012, 2012.
George, C., Strekowski, R. S., Kleffmann, J., Stemmler, K., and Ammann, M.: Photoenhanced uptake of gaseous NO2 on solid organic compounds: a photochemical source of HONO?, Faraday Discuss., 130, 195–210, 2005.
Gustafsson, R. J., Kyriakou, G., and Lambert, R. M.: The molecular mechanism of tropospheric nitrous acid production on mineral dust surfaces, ChemPhysChem, 9, 1390–1393, 2008.
Gutzwiller, L., George, C., Rössler, E., and Ammann, M.: Reaction kinetics of NO2 with resorcinol and 2,7-naphthalenediol in the aqueous phase at different pH, J. Phys. Chem. A, 106, 12045–12050, 2002.
Harrison, R. M. and Kitto, A.-M. N.: Evidence for a surface source of atmospheric nitrous acid, Atmos. Environ., 28, 1089–1094, 1994.
Harrison, R. M., Peak, J. D., and Collin, G. M.: Tropospheric cycle of nitrous acid, J. Geophys. Res., 101, 14429–14439, 1996.
Heland, J., Kleffmann, J., Kurtenbach, R., and Wiesen, P.: A new instrument to measure gaseous nitrous acid (HONO) in the atmosphere, Environ. Sci. Technol., 35, 3207–3212, 2001.
Kamboures, M. A., Raff, J. D., Miller, Y., Phillips, L. F., Finlayson-Pitts, B. J., and Gerber, R. B.: Complexes of HNO3 and NO3 with NO2 and N2O4, and their potential role in atmospheric HONO formation, Phys. Chem. Chem. Phys., 10, 6019–6032, 2008.
Kleffmann, J.: Daytime sources of nitrous acid (HONO) in the atmospheric boundary layer, ChemPhysChem, 8, 1137–1144, 2007.
Kleffmann, J., Becker, K. H., Lackhoff, M., and Wiesen, P.: Heterogeneous conversion of NO2 on carbonaceous surfaces, Phys. Chem. Chem. Phys., 1, 5443–5450, 1999.
Kleffmann, J., Heland, J., Kurtenbach, R., Lörzer, J., and Wiesen, P.: A new instrument (LOPAP) for the detection of nitrous acid (HONO), Environ. Sci. Pollut. R., 4, 48–54, 2002.
Kleffmann, J., Gavriloaiei, T., Hofzumahaus, A., Holland, F., Koppmann, R., Rupp, L., Schlosser, E., Siese, M., and Wahner, A.: Daytime formation of nitrous acid: A major source of OH radicals in a forest, Geophys. Res. Lett., 32, L05818, https://doi.org/10.1029/2005GL022524, 2005.
Kubota, M. and Asami, T.: Source of nitrous acid volatilized from upland soils, Soil Sci. Plant Nutr., 31, 35–42, 1985.
Lee, B. H., Wood, E. C., Herndon, S. C., Lefer, B. L., Luke, W. T., Brune, W. H., Nelson, D. D., Zahniser, M. S., and Munger, J. W.: Urban measurements of atmospheric nitrous acid: A caveat on the interpretation of the HONO photostationary state, J. Geophys. Res., 118, 1–8, https://doi.org/10.1002/2013JD020341, 2013.
Li, X., Rohrer, F., Hofzumahaus, H., Brauers, T., Häseler, R., Bohn, B., Broch, S., Fuchs, H., Gomm, S., Holland, F., Jäger, J., Kaiser, J., Keutsch, F. N., Lohse, I., Lu, K., Tillmann, R., Wegener, R., Wolfe, G. M., F. Mentel, T. F., Kiendler-Scharr, A., and Wahner, A.: Missing gas-phase source of HONO inferred from zeppelin measurements in the troposphere, Science, 344, 292–296, https://doi.org/10.1126/science.1248999, 2014.
Ludwig, J., Meixner, F. X., Vogel, B., and Förstner J.: Soil-air exchange of nitric oxide: An overview of processes, environmental factors, and modeling studies, Biogeochemistry, 52, 225–257, 2001.
Madronich, S. and Flocke, S.: The role of solar radiation in atmospheric chemistry, in The Handbook of Environmental Chemistry/Reactions and Processes/Environmental Photochemistry Part I: BD 2 / Part L, edited by: Boule, P., Springer-Verlag, Heidelberg, Germany, 373, 1–26, 1998.
Maljanen, M., Yli-Pirilä, P., Hytönen, J., Joutsensaari, J., and Martikainen, P. J.: Acidic northern soils as sources of atmospheric nitrous acid (HONO), Soil Biol. Biochem., 67, 94–97, https://doi.org/10.1016/j.soilbio.2013.08.013, 2013.
Matthies, C., Erhard, H.-P., and Drake, H. L.: Effects of pH on the comparative culturability of fungi and bacteria from acidic and less acidic forest soils, J. Basic. Microb., 37, 335–343, 1997.
Mauder, M. and Foken, T.: Documentation and instruction manual of the eddy-covariance software package TK3, Universität Bayreuth, Abteilung Mikrometeorologie, 46, 60 pp., ISSN1614-8924, 2011.
Miller, Y., Finlayson-Pitts, B. J., and Gerber, R. B.: Ionization of N2O4 in contact with water: mechanism, time scales and atmospheric implications, J. Am. Chem. Soc., 131, 12180–12185, https://doi.org/10.1021/ja900350g, 2009.
Moldrup, P., Olesen, T., Gamst, J., Schjonning, P., Yamaguchi, T., and Rolston, D. E.: Predicting the gas diffusion coefficient in repacked soil: Water-induced linear reduction model, Soil Sci. Soc. Am. J., 64, 1588–1594, 2000.
Oren, R., Schulze, E.-D., Matyssek, R., and Zimmermann, R.: Estimating photosynthetic rate and annual carbon gain in conifers from specific leaf weight and leaf biomass, Oecologia, 70, 187–193, 1986.
Oswald, R., Behrendt, T., Ermel, M., Wu, D., Su, H., Cheng, Y., Breuninger, C., Moravek, A., Mougin, Delon, C., Loubet, B., Pommerening-Röser, A., Sörgel, M., Pöschl, U., Hoffmann, T., Andreae, M. O., Meixner, F. X., and Trebs, I.: HONO emissions from soil bacteria as a major source of atmospheric reactive Nitrogen, Science, 341, 1233–1235, https://doi.org/10.1126/science.1242266, 2013.
Oswald, R., Ermel, M., Hens, K., Novelli, A., Ouwersloot, H. G., Paasonen, P., Petäjä, T., Sipilä, M., Keronen, P., Bäck, J., Königstedt, R., Hosaynali Beygi, Z., Fischer, H., Bohn, B., Kubistin, D., Harder, H., Martinez, M., Williams, J., Hoffmann, T., Trebs, I., and Sörgel, M.: A comparison of HONO budgets for two measurement heights at a field station within the boreal forest in Finland, Atmos. Chem. Phys., 15, 799–813, https://doi.org/10.5194/acp-15-799-2015, 2015.
Pape, L., Ammann, C., Nyfeler-Brunner, A., Spirig, C., Hens, K., and Meixner, F. X.: An automated dynamic chamber system for surface exchange measurement of non-reactive and reactive trace gases of grassland ecosystems, Biogeosciences, 6, 405–429, https://doi.org/10.5194/bg-6-405-2009, 2009.
Ramazan, K. A., Syomin, D., and Finlayson-Pitts, B. J.: The photochemical production of HONO during the heterogeneous hydrolysis of NO2, Phys. Chem. Chem. Phys., 6, 3836–3843, 2004.
Ren, X., Sanders, J. E., Rajendran, A., Weber, R. J., Goldstein, A. H., Pusede, S. E., Browne, E. C., Min, K.-E., and Cohen, R. C.: A relaxed eddy accumulation system for measuring vertical fluxes of nitrous acid, Atmos. Meas. Tech., 4, 2093–2103, https://doi.org/10.5194/amt-4-2093-2011, 2011.
Rousk, J., Bååth, E., Brookes, P. C., Lauber, C. L., Lozupone, C., Caporaso, J. G., Knight, R., and Fierer, N.: Soil bacterial and fungal communities across a pH gradient in an arable soil, ISME J., 4, 1340–1351, 2010.
Rubasinghege, G. and Grassian V. H.: Photochemistry of adsorbed nitrate on aluminum oxide particle surfaces, J. Phys. Chem. A, 113, 7818–7825, 2009.
Scharko, N. K., Berke, A. E., and Raff, J. D.: Release of nitrous acid and nitrogen dioxide from nitrate photolysis in acidic aqueous solutions, Environ. Sci. Technol., 48, 11991–12001, https://doi.org/10.1021/es503088x, 2014.
Schimang R., Folkers A., Kleffmann J., Kleist E., Miebach M., and Wildt J.: Uptake of Gaseous Nitrous Acid (HONO) by Several Plant Species, Atmos. Environ., 40, 1324–1335, 2006.
Schuttlefield, J., Rubasinghege, G., El-Maazawi, M., Bone, J., and Grassian, V. H.: Photochemistry of adsorbed nitrate, J. Am. Chem. Soc., 130, 12210–12211, 2008.
Sörgel, M., Regelin, E., Bozem, H., Diesch, J.-M., Drewnick, F., Fischer, H., Harder, H., Held, A., Hosaynali-Beygi, Z., Martinez, M., and Zetzsch, C.: Quantification of the unknown HONO daytime source and its relation to NO2, Atmos. Chem. Phys., 11, 10433–10447, https://doi.org/10.5194/acp-11-10433-2011, 2011a.
Sörgel, M., Trebs, I., Serafimovich, A., Moravek, A., Held, A., and Zetzsch, C.: Simultaneous HONO measurements in and above a forest canopy: influence of turbulent exchange on mixing ratio differences, Atmos. Chem. Phys., 11, 841–855, https://doi.org/10.5194/acp-11-841-2011, 2011b.
Stemmler, K., Ammann, M., Donders, C., Kleffmann, J., and George, C.: Photosensitized reduction of nitrogen dioxide on humic acid as a source of nitrous acid, Nature, 440, 195–198, 2006.
Stemmler, K., Ndour, M., Elshorbany, Y., Kleffmann, J., D'Anna, B., George, C., Bohn, B., and Ammann, M.: Light induced conversion of nitrogen dioxide into nitrous acid on submicron humic acid aerosol, Atmos. Chem. Phys., 7, 4237–4248, https://doi.org/10.5194/acp-7-4237-2007, 2007.
Stutz, J., Alicke, B., and Neftel, A.: Nitrous acid formation in the urban atmosphere: Gradient measurements of NO2 and HONO over grass in Milan, Italy, J. Geophys. Res., 107, 8192, https://doi.org/10.1029/2001JD000390, 2002.
Su, H., Cheng, Y. F., Shao, M., Gao, D. F., Yu, Z. Y., Zeng, L. M., Slanina, J., Zhang, Y. H., and Wiedensohler, A.: Nitrous acid (HONO) and its daytime sources at a rural site during the 2004 PRIDE-PRD experiment in China, J. Geophys. Res., 113, D14312, https://doi.org/10.1029/2007JD009060, 2008.
Su, H., Cheng,Y., Oswald, R., Behrendt, T., Trebs, I., Meixner, F.-X., Andreae, M. O., Cheng, P., Zhang, Y., and Pöschl, U.: Soil nitrite as a source of atmospheric HONO and OH radicals, Science, 333, 1616–1618, https://doi.org/10.1126/science.1207687, 2011.
Trebs, I., Bohn, B., Ammann, C., Rummel, U., Blumthaler, M., Königstedt, R., Meixner, F. X., Fan, S., and Andreae, M. O.: Relationship between the NO2 photolysis frequency and the solar global irradiance, Atmos. Meas. Tech., 2, 725–739, https://doi.org/10.5194/amt-2-725-2009, 2009.
Van Cleemput, O. and Baert, L.: Nitrite: a key compound in N loss processes under acid conditions?, Plant Soil, 76, 233–241, 1984.
VandenBoer, T. C., Brown, S. S., Murphy, J. G., Keene, W. C., Young, C. J., Pszenny, A. A. P., Kim, S., Warneke, C., de Gouw, J. A., Maben, J. R., Wagner, N. L., Riedel, T. P., Thornton, J. A., Wolfe, D. E., Dubé, W. P., Öztürk, F., Brock, C. A., Grossberg, N., Lefer, B., Lerner, B., Middlebrook, A. M., and Roberts, J. M.: Understanding the role of the ground surface in HONO vertical structure: High resolution vertical profiles during NACHTT-11, J. Geophys. Res.-Atmos., 118, 10155–10171, https://doi.org/10.1002/jgrd.50721, 2013.
VandenBoer, T. C., Young, C. J., Talukdar, R. K., Markovic, M. Z., Brown, S. S., Roberts, J. M., and Murphy, J. G.: Nocturnal loss and daytime source of nitrous acid through reactive uptake and displacement, Nat. Geosci., 8, 5–7, https://doi.org/10.1038/ngeo2315, 2015.
Venterea, R. T., Rolston, D. E., and Cardon, Z. G.: Effects of soil moisture, physical, and chemical characteristics on abiotic nitric oxide production, Nutr. Cycl. Agroecosys., 72, 27–40, 2005.
Volkamer, R., Sheehy, P., Molina, L. T., and Molina, M. J.: Oxidative capacity of the Mexico City atmosphere – Part 1: A radical source perspective, Atmos. Chem. Phys., 10, 6969–6991, https://doi.org/10.5194/acp-10-6969-2010, 2010.
Wolff, V., Trebs, I., Ammann, C., and Meixner, F. X.: Aerodynamic gradient measurements of the NH3-HNO3-NH4NO3 triad using a wet chemical instrument: an analysis of precision requirements and flux errors, Atmos. Meas. Tech., 3, 187–208, https://doi.org/10.5194/amt-3-187-2010, 2010.
Wong, K. W., Oh, H.-J., Lefer, B. L., Rappenglück, B., and Stutz, J.: Vertical profiles of nitrous acid in the nocturnal urban atmosphere of Houston, TX, Atmos. Chem. Phys., 11, 3595–3609, https://doi.org/10.5194/acp-11-3595-2011, 2011.
Wong, K. W., Tsai, C., Lefer, B., Haman, C., Grossberg, N., Brune, W. H., Ren, X., Luke, W., and Stutz, J.: Daytime HONO vertical gradients during SHARP 2009 in Houston, TX, Atmos. Chem. Phys., 12, 635–652, https://doi.org/10.5194/acp-12-635-2012, 2012.
Wong, K. W., Tsai, C., Lefer, B., Grossberg, N., and Stutz, J.: Modeling of daytime HONO vertical gradients during SHARP 2009, Atmos. Chem. Phys., 13, 3587–3601, https://doi.org/10.5194/acp-13-3587-2013, 2013.
Yabushita, A., Enami, S., Sakamoto, Y., Kawasaki, M., Hoffmann, M. R., and Colussi, A. J.: Anion-catalyzed dissolution of NO2 on aqueous microdroplets, J. Phys. Chem. A, 113, 4844–4848, 2009.
Zhang, N., Zhou, X., Shepson, P. B., Gao, H., Alaghmand, M., and Stirm, B.: Aircraft measurement of HONO vertical profiles over a forested region, Geophys. Res. Lett., 36, L15820, https://doi.org/10.1029/2009GL038999, 2009.
Zhang, N., Zhou, X., Bertman, S., Tang, D., Alaghmand, M., Shepson, P. B., and Carroll, M. A.: Measurements of ambient HONO concentrations and vertical HONO flux above a northern Michigan forest canopy, Atmos. Chem. Phys., 12, 8285–8296, https://doi.org/10.5194/acp-12-8285-2012, 2012.
Zhou, X., He, Y., Huang, G., Thornberry, T. D., Carroll, M. A., and Bertman, S. B.: Photochemical production of nitrous acid on glass sample manifold surface, Geophys. Res. Lett., 29, 1681, https://doi.org/10.1029/2002GL015080, 2002.
Zhou, X., Gao, H., He, Y., Huang, G., Bertman, S. B., Civerolo, K., and Schwab, J.: Nitric acid photolysis on surfaces in low-NOx environments: Significant atmospheric implications, Geophys. Res. Lett., 30, 1–4, 2003.
Zhou, X. L., Zhang, N., TerAvest, M., Tang, D., Hou, J., Bertman, S., Alaghmand, M., Shepson, P. B., Carroll, M. A., Griffith, S., Dusanter, S., and Stevens, P. S.: Nitric acid photolysis on forest canopy surface as a source for tropospheric nitrous acid, Nat. Geosci., 4, 440–443, https://doi.org/10.1038/ngeo1164, 2011.
Zhu, C., Xiang, B., Zhu, L., and Cole, R.: Determination of absorption cross sections of surface-adsorbed HNO3 in the 290–330 nm region by Brewster angle cavity ring-down spectroscopy, Chem. Phys. Lett., 458, 73–377, 2008.
Zhu, C., Xiang, B., Chu, L. T., and Zhu, L.: Photolysis of Nitric Acid in the Gas Phase, on Aluminum Surfaces, and on Ice Films, J. Phys. Chem. A, 114, 2561–2568, 2010.
Short summary
We measured near-surface (< 2m) profiles of HONO in a clearing and on a forest floor. Both HONO deposition and emissions were observed. By comparing three postulated sources to observed daytime emissions, we made several important findings: ● conversion of NO2 is mostly independent of light due to light saturation ● HONO emissions from a very acidic soil were low ● photolysis of adsorbed HNO3 could serve as HONO source based on empirical parameters but unlikely via the proposed reaction pathway.
We measured near-surface ( 2m) profiles of HONO in a clearing and on a forest floor. Both HONO...
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