Articles | Volume 13, issue 6
Atmos. Chem. Phys., 13, 3363–3378, 2013
https://doi.org/10.5194/acp-13-3363-2013
© Author(s) 2013. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Special issue: The TransBrom Sonne ship campaign in the West Pacific
Atmos. Chem. Phys., 13, 3363–3378, 2013
https://doi.org/10.5194/acp-13-3363-2013
© Author(s) 2013. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Research article
25 Mar 2013
Research article
| 25 Mar 2013
Iodine monoxide in the Western Pacific marine boundary layer
K. Großmann et al.
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Atmos. Chem. Phys., 16, 12239–12271, https://doi.org/10.5194/acp-16-12239-2016, https://doi.org/10.5194/acp-16-12239-2016, 2016
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C. Prados-Roman, C. A. Cuevas, T. Hay, R. P. Fernandez, A. S. Mahajan, S.-J. Royer, M. Galí, R. Simó, J. Dachs, K. Großmann, D. E. Kinnison, J.-F. Lamarque, and A. Saiz-Lopez
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Gaia Pinardi, Michel Van Roozendael, François Hendrick, Andreas Richter, Pieter Valks, Ramina Alwarda, Kristof Bognar, Udo Frieß, José Granville, Myojeong Gu, Paul Johnston, Cristina Prados-Roman, Richard Querel, Kimberly Strong, Thomas Wagner, Folkard Wittrock, and Margarita Yela Gonzalez
Atmos. Meas. Tech., 15, 3439–3463, https://doi.org/10.5194/amt-15-3439-2022, https://doi.org/10.5194/amt-15-3439-2022, 2022
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We report on the GOME-2A and GOME-2B OClO dataset (2007 to 2016, from the EUMETSAT's AC SAF) validation using data from nine NDACC zenith-scattered-light DOAS (ZSL-DOAS) instruments distributed in both the Arctic and Antarctic. Specific sensitivity tests are performed on the ground-based data to estimate the impact of the different OClO DOAS analysis settings and their typical errors. Good agreement is found for both the inter-annual variability and the overall OClO seasonal behavior.
Susann Tegtmeier, Christa Marandino, Yue Jia, Birgit Quack, and Anoop S. Mahajan
Atmos. Chem. Phys., 22, 6625–6676, https://doi.org/10.5194/acp-22-6625-2022, https://doi.org/10.5194/acp-22-6625-2022, 2022
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Maximilian Herrmann, Moritz Schöne, Christian Borger, Simon Warnach, Thomas Wagner, Ulrich Platt, and Eva Gutheil
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2022-334, https://doi.org/10.5194/acp-2022-334, 2022
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M. Dolores Andrés Hernández, Andreas Hilboll, Helmut Ziereis, Eric Förster, Ovid O. Krüger, Katharina Kaiser, Johannes Schneider, Francesca Barnaba, Mihalis Vrekoussis, Jörg Schmidt, Heidi Huntrieser, Anne-Marlene Blechschmidt, Midhun George, Vladyslav Nenakhov, Theresa Harlass, Bruna A. Holanda, Jennifer Wolf, Lisa Eirenschmalz, Marc Krebsbach, Mira L. Pöhlker, Anna B. Kalisz Hedegaard, Linlu Mei, Klaus Pfeilsticker, Yangzhuoran Liu, Ralf Koppmann, Hans Schlager, Birger Bohn, Ulrich Schumann, Andreas Richter, Benjamin Schreiner, Daniel Sauer, Robert Baumann, Mariano Mertens, Patrick Jöckel, Markus Kilian, Greta Stratmann, Christopher Pöhlker, Monica Campanelli, Marco Pandolfi, Michael Sicard, José L. Gómez-Amo, Manuel Pujadas, Katja Bigge, Flora Kluge, Anja Schwarz, Nikos Daskalakis, David Walter, Andreas Zahn, Ulrich Pöschl, Harald Bönisch, Stephan Borrmann, Ulrich Platt, and John P. Burrows
Atmos. Chem. Phys., 22, 5877–5924, https://doi.org/10.5194/acp-22-5877-2022, https://doi.org/10.5194/acp-22-5877-2022, 2022
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Jan-Lukas Tirpitz, Udo Frieß, Robert Spurr, and Ulrich Platt
Atmos. Meas. Tech., 15, 2077–2098, https://doi.org/10.5194/amt-15-2077-2022, https://doi.org/10.5194/amt-15-2077-2022, 2022
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Guangyu Liu, Toshihiko Hirooka, Nawo Eguchi, and Kirstin Krüger
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Atmos. Meas. Tech., 15, 1395–1414, https://doi.org/10.5194/amt-15-1395-2022, https://doi.org/10.5194/amt-15-1395-2022, 2022
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Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2022-119, https://doi.org/10.5194/acp-2022-119, 2022
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Jonas Kuhn, Nicole Bobrowski, Thomas Wagner, and Ulrich Platt
Atmos. Meas. Tech., 14, 7873–7892, https://doi.org/10.5194/amt-14-7873-2021, https://doi.org/10.5194/amt-14-7873-2021, 2021
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We propose spectrograph implementations using Fabry–Pérot interferometers for atmospheric trace gas remote sensing. Compared with widely used grating spectrographs, we find substantial light throughput and mobility advantages for high resolving powers. Besides lowering detection limits and increasing the spatial and temporal resolution of many atmospheric trace gas measurements, this approach might enable remote sensing of further important gases such as tropospheric OH radicals.
Jānis Puķīte, Christian Borger, Steffen Dörner, Myojeong Gu, Udo Frieß, Andreas Carlos Meier, Carl-Fredrik Enell, Uwe Raffalski, Andreas Richter, and Thomas Wagner
Atmos. Meas. Tech., 14, 7595–7625, https://doi.org/10.5194/amt-14-7595-2021, https://doi.org/10.5194/amt-14-7595-2021, 2021
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Chlorine dioxide (OClO) is used as an indicator for chlorine activation. We present a new differential optical absorption spectroscopy retrieval algorithm for OClO from measurements of TROPOMI on the Sentinel-5P satellite. To achieve a substantially improved accuracy for the weak absorber OClO, we consider several additional fit parameters accounting for various higher-order spectral effects. The retrieved OClO slant column densities are compared with ground-based zenith sky measurements.
Phuc Thi Minh Ha, Yugo Kanaya, Fumikazu Taketani, Maria Dolores Andrés Hernández, Benjamin Schreiner, Klaus Pfeilsticker, and Kengo Sudo
Geosci. Model Dev. Discuss., https://doi.org/10.5194/gmd-2021-385, https://doi.org/10.5194/gmd-2021-385, 2021
Preprint under review for GMD
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HONO affects tropospheric oxidizing capacity; thus is implemented into the chemistry-climate model CHASER. The model substantially underpredicts daytime HONO due to low emission and low NO2 uptakes on aerosol and cloud. Current HONO chemistry predicts reductions for 20.4 % global tropospheric NOx, 40–67 % OH and 30–45 % O3 in summer North Pacific. In contrast, OH and O3 winter levels in China are hugely enhanced. Future work needs elaborate HONO mechanisms and an efficient NOx-recycle process.
Paul D. Hamer, Virginie Marécal, Ryan Hossaini, Michel Pirre, Gisèle Krysztofiak, Franziska Ziska, Andreas Engel, Stephan Sala, Timo Keber, Harald Bönisch, Elliot Atlas, Kirstin Krüger, Martyn Chipperfield, Valery Catoire, Azizan A. Samah, Marcel Dorf, Phang Siew Moi, Hans Schlager, and Klaus Pfeilsticker
Atmos. Chem. Phys., 21, 16955–16984, https://doi.org/10.5194/acp-21-16955-2021, https://doi.org/10.5194/acp-21-16955-2021, 2021
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Bromoform is a stratospheric ozone-depleting gas released by seaweed and plankton transported to the stratosphere via convection in the tropics. We study the chemical interactions of bromoform and its derivatives within convective clouds using a cloud-scale model and observations. Our findings are that soluble bromine gases are efficiently washed out and removed within the convective clouds and that most bromine is transported vertically to the upper troposphere in the form of bromoform.
Ulrich Platt, Thomas Wagner, Jonas Kuhn, and Thomas Leisner
Atmos. Meas. Tech., 14, 6867–6883, https://doi.org/10.5194/amt-14-6867-2021, https://doi.org/10.5194/amt-14-6867-2021, 2021
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Absorption spectroscopy of scattered sunlight is extremely useful for the analysis of atmospheric trace gas distributions. A central parameter for the achievable sensitivity of spectroscopic instruments is the light throughput, which can be enhanced in a number of ways. We present new ideas and considerations of how instruments could be optimized. Particular emphasis is on arrays of massively parallel instruments. Such arrays can reduce the size and weight of instruments by orders of magnitude.
Clara M. Nussbaumer, Uwe Parchatka, Ivan Tadic, Birger Bohn, Daniel Marno, Monica Martinez, Roland Rohloff, Hartwig Harder, Flora Kluge, Klaus Pfeilsticker, Florian Obersteiner, Martin Zöger, Raphael Doerich, John N. Crowley, Jos Lelieveld, and Horst Fischer
Atmos. Meas. Tech., 14, 6759–6776, https://doi.org/10.5194/amt-14-6759-2021, https://doi.org/10.5194/amt-14-6759-2021, 2021
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NO2 plays a central role in atmospheric photochemical processes and requires accurate measurements. This research presents NO2 data obtained via chemiluminescence using a photolytic converter from airborne studies around Cabo Verde and laboratory investigations. We show the limits and error-proneness of a conventional blue light converter in aircraft measurements affected by humidity and NO levels and suggest the use of an alternative quartz converter for more reliable results.
Meike K. Rotermund, Vera Bense, Martyn P. Chipperfield, Andreas Engel, Jens-Uwe Grooß, Peter Hoor, Tilman Hüneke, Timo Keber, Flora Kluge, Benjamin Schreiner, Tanja Schuck, Bärbel Vogel, Andreas Zahn, and Klaus Pfeilsticker
Atmos. Chem. Phys., 21, 15375–15407, https://doi.org/10.5194/acp-21-15375-2021, https://doi.org/10.5194/acp-21-15375-2021, 2021
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Airborne total bromine (Brtot) and tracer measurements suggest Brtot-rich air masses persistently protruded into the lower stratosphere (LS), creating a high Brtot region over the North Atlantic in fall 2017. The main source is via isentropic transport by the Asian monsoon and to a lesser extent transport across the extratropical tropopause as quantified by a Lagrange model. The transport of Brtot via Central American hurricanes is also observed. Lastly, the impact of Brtot on LS O3 is assessed.
Florian Dinger, Timo Kleinbek, Steffen Dörner, Nicole Bobrowski, Ulrich Platt, Thomas Wagner, Martha Ibarra, and Eveling Espinoza
Atmos. Chem. Phys., 21, 9367–9404, https://doi.org/10.5194/acp-21-9367-2021, https://doi.org/10.5194/acp-21-9367-2021, 2021
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Monitoring magnitude or chemical composition of volcanic gas emissions can help to forecast volcanic eruptions and provides empirical data on the impact of volcanoes on the chemistry in the local and global atmosphere. This study reports and discusses continuous time series of the sulfur and bromine emission fluxes of Masaya from 2014 to 2020. We observed an annual cyclicity in the BrO / SO2 molar ratio, possibly caused by the annual variability in the atmospheric humidity.
Maximilian Herrmann, Holger Sihler, Udo Frieß, Thomas Wagner, Ulrich Platt, and Eva Gutheil
Atmos. Chem. Phys., 21, 7611–7638, https://doi.org/10.5194/acp-21-7611-2021, https://doi.org/10.5194/acp-21-7611-2021, 2021
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Time-dependent 3D numerical simulations of tropospheric bromine release and ozone depletion events (ODEs) in the Arctic polar spring of 2009 are compared to observations. Simulation results agree well with the observations at both Utqiaġvik, Alaska, and at Summit, Greenland. In a parameter study, different settings for the bromine release mechanism are evaluated. An enhancement of the bromine release mechanism improves the agreement regarding the occurrence of ODEs with the observations.
Evelien van Dijk, Johann Jungclaus, Stephan Lorenz, Claudia Timmreck, and Kirstin Krüger
Clim. Past Discuss., https://doi.org/10.5194/cp-2021-49, https://doi.org/10.5194/cp-2021-49, 2021
Revised manuscript accepted for CP
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A double volcanic eruption in 536 and 540 AD caused one of the coldest decades during the last 2000 years. We analyze new climate model simulations from that period. We found a cooling of up to 2 °C and a sea–ice extent up to 200 km further south. Complex interactions between sea–ice and ocean circulation lead to a reduction in the northward ocean heat transport, which makes the sea-ice extend further south, which in turn leads to a surface cooling up to 20 years after the eruptions.
Santiago Arellano, Bo Galle, Fredy Apaza, Geoffroy Avard, Charlotte Barrington, Nicole Bobrowski, Claudia Bucarey, Viviana Burbano, Mike Burton, Zoraida Chacón, Gustavo Chigna, Christian Joseph Clarito, Vladimir Conde, Fidel Costa, Maarten De Moor, Hugo Delgado-Granados, Andrea Di Muro, Deborah Fernandez, Gustavo Garzón, Hendra Gunawan, Nia Haerani, Thor H. Hansteen, Silvana Hidalgo, Salvatore Inguaggiato, Mattias Johansson, Christoph Kern, Manne Kihlman, Philippe Kowalski, Pablo Masias, Francisco Montalvo, Joakim Möller, Ulrich Platt, Claudia Rivera, Armando Saballos, Giuseppe Salerno, Benoit Taisne, Freddy Vásconez, Gabriela Velásquez, Fabio Vita, and Mathieu Yalire
Earth Syst. Sci. Data, 13, 1167–1188, https://doi.org/10.5194/essd-13-1167-2021, https://doi.org/10.5194/essd-13-1167-2021, 2021
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This study presents a dataset of volcanic sulfur dioxide (SO2) emissions from 2005–2017. Measurements were obtained by Network for Observation of Volcanic and Atmospheric Change (NOVAC) scanning differential optical absorption spectrometer (ScanDOAS) instruments at 32 volcanoes and processed using a standardized procedure. We show statistics of volcanic gas emissions under a variety of conditions and compare them with averages derived from measurements from space and historical inventories.
Josefine Maas, Susann Tegtmeier, Yue Jia, Birgit Quack, Jonathan V. Durgadoo, and Arne Biastoch
Atmos. Chem. Phys., 21, 4103–4121, https://doi.org/10.5194/acp-21-4103-2021, https://doi.org/10.5194/acp-21-4103-2021, 2021
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Cooling-water disinfection at coastal power plants is a known source of atmospheric bromoform. A large source of anthropogenic bromoform is the industrial regions in East Asia. In current bottom-up flux estimates, these anthropogenic emissions are missing, underestimating the global air–sea flux of bromoform. With transport simulations, we show that by including anthropogenic bromoform from cooling-water treatment, the bottom-up flux estimates significantly improve in East and Southeast Asia.
Christopher Fuchs, Jonas Kuhn, Nicole Bobrowski, and Ulrich Platt
Atmos. Meas. Tech., 14, 295–307, https://doi.org/10.5194/amt-14-295-2021, https://doi.org/10.5194/amt-14-295-2021, 2021
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We present first measurements of volcanic SO2 emissions with a novel imaging technique for atmospheric trace gases in the UV and visible spectral range. Periodic spectral Fabry–Pérot interferometer transmission features are matched to differential absorption cross sections of the investigated trace gas, yielding high selectivity and sensitivity. The technique can be extended to measure many other trace gases with high spatio-temporal resolution.
Jan-Lukas Tirpitz, Udo Frieß, François Hendrick, Carlos Alberti, Marc Allaart, Arnoud Apituley, Alkis Bais, Steffen Beirle, Stijn Berkhout, Kristof Bognar, Tim Bösch, Ilya Bruchkouski, Alexander Cede, Ka Lok Chan, Mirjam den Hoed, Sebastian Donner, Theano Drosoglou, Caroline Fayt, Martina M. Friedrich, Arnoud Frumau, Lou Gast, Clio Gielen, Laura Gomez-Martín, Nan Hao, Arjan Hensen, Bas Henzing, Christian Hermans, Junli Jin, Karin Kreher, Jonas Kuhn, Johannes Lampel, Ang Li, Cheng Liu, Haoran Liu, Jianzhong Ma, Alexis Merlaud, Enno Peters, Gaia Pinardi, Ankie Piters, Ulrich Platt, Olga Puentedura, Andreas Richter, Stefan Schmitt, Elena Spinei, Deborah Stein Zweers, Kimberly Strong, Daan Swart, Frederik Tack, Martin Tiefengraber, René van der Hoff, Michel van Roozendael, Tim Vlemmix, Jan Vonk, Thomas Wagner, Yang Wang, Zhuoru Wang, Mark Wenig, Matthias Wiegner, Folkard Wittrock, Pinhua Xie, Chengzhi Xing, Jin Xu, Margarita Yela, Chengxin Zhang, and Xiaoyi Zhao
Atmos. Meas. Tech., 14, 1–35, https://doi.org/10.5194/amt-14-1-2021, https://doi.org/10.5194/amt-14-1-2021, 2021
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Multi-axis differential optical absorption spectroscopy (MAX-DOAS) is a ground-based remote sensing measurement technique that derives atmospheric aerosol and trace gas vertical profiles from skylight spectra. In this study, consistency and reliability of MAX-DOAS profiles are assessed by applying nine different evaluation algorithms to spectral data recorded during an intercomparison campaign in the Netherlands and by comparing the results to colocated supporting observations.
Gaia Pinardi, Michel Van Roozendael, François Hendrick, Nicolas Theys, Nader Abuhassan, Alkiviadis Bais, Folkert Boersma, Alexander Cede, Jihyo Chong, Sebastian Donner, Theano Drosoglou, Anatoly Dzhola, Henk Eskes, Udo Frieß, José Granville, Jay R. Herman, Robert Holla, Jari Hovila, Hitoshi Irie, Yugo Kanaya, Dimitris Karagkiozidis, Natalia Kouremeti, Jean-Christopher Lambert, Jianzhong Ma, Enno Peters, Ankie Piters, Oleg Postylyakov, Andreas Richter, Julia Remmers, Hisahiro Takashima, Martin Tiefengraber, Pieter Valks, Tim Vlemmix, Thomas Wagner, and Folkard Wittrock
Atmos. Meas. Tech., 13, 6141–6174, https://doi.org/10.5194/amt-13-6141-2020, https://doi.org/10.5194/amt-13-6141-2020, 2020
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We validate several GOME-2 and OMI tropospheric NO2 products with 23 MAX-DOAS and 16 direct sun instruments distributed worldwide, highlighting large horizontal inhomogeneities at several sites affecting the validation results. We propose a method for quantification and correction. We show the application of such correction reduces the satellite underestimation in almost all heterogeneous cases, but a negative bias remains over the MAX-DOAS and direct sun network ensemble for both satellites.
Flora Kluge, Tilman Hüneke, Matthias Knecht, Michael Lichtenstern, Meike Rotermund, Hans Schlager, Benjamin Schreiner, and Klaus Pfeilsticker
Atmos. Chem. Phys., 20, 12363–12389, https://doi.org/10.5194/acp-20-12363-2020, https://doi.org/10.5194/acp-20-12363-2020, 2020
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The presented study reports on airborne measurements of formaldehyde, glyoxal, methylglyoxal, and CO over the Amazon basin and lays a special focus on the influence of biomass burning emissions on the atmospheric profiles of these carbonyl compounds within the planetary boundary layer as well as in the free and upper troposphere.
Yang Wang, Arnoud Apituley, Alkiviadis Bais, Steffen Beirle, Nuria Benavent, Alexander Borovski, Ilya Bruchkouski, Ka Lok Chan, Sebastian Donner, Theano Drosoglou, Henning Finkenzeller, Martina M. Friedrich, Udo Frieß, David Garcia-Nieto, Laura Gómez-Martín, François Hendrick, Andreas Hilboll, Junli Jin, Paul Johnston, Theodore K. Koenig, Karin Kreher, Vinod Kumar, Aleksandra Kyuberis, Johannes Lampel, Cheng Liu, Haoran Liu, Jianzhong Ma, Oleg L. Polyansky, Oleg Postylyakov, Richard Querel, Alfonso Saiz-Lopez, Stefan Schmitt, Xin Tian, Jan-Lukas Tirpitz, Michel Van Roozendael, Rainer Volkamer, Zhuoru Wang, Pinhua Xie, Chengzhi Xing, Jin Xu, Margarita Yela, Chengxin Zhang, and Thomas Wagner
Atmos. Meas. Tech., 13, 5087–5116, https://doi.org/10.5194/amt-13-5087-2020, https://doi.org/10.5194/amt-13-5087-2020, 2020
Rui Cheng, Troy S. Magney, Debsunder Dutta, David R. Bowling, Barry A. Logan, Sean P. Burns, Peter D. Blanken, Katja Grossmann, Sophia Lopez, Andrew D. Richardson, Jochen Stutz, and Christian Frankenberg
Biogeosciences, 17, 4523–4544, https://doi.org/10.5194/bg-17-4523-2020, https://doi.org/10.5194/bg-17-4523-2020, 2020
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We measured reflected sunlight from an evergreen canopy for a year to detect changes in pigments that play an important role in regulating the seasonality of photosynthesis. Results show a strong mechanistic link between spectral reflectance features and pigment content, which is validated using a biophysical model. Our results show spectrally where, why, and when spectral features change over the course of the season and show promise for estimating photosynthesis remotely.
Jonathon S. Wright, Xiaoyi Sun, Paul Konopka, Kirstin Krüger, Bernard Legras, Andrea M. Molod, Susann Tegtmeier, Guang J. Zhang, and Xi Zhao
Atmos. Chem. Phys., 20, 8989–9030, https://doi.org/10.5194/acp-20-8989-2020, https://doi.org/10.5194/acp-20-8989-2020, 2020
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High clouds are influential in tropical climate. Although reanalysis cloud fields are essentially model products, they are indirectly constrained by observations and offer global coverage with direct links to advanced water and energy cycle metrics, giving them many useful applications. We describe how high cloud fields are generated in reanalyses, assess their realism and reliability in the tropics, and evaluate how differences in these fields affect other aspects of the reanalysis state.
James Barry, Dirk Böttcher, Klaus Pfeilsticker, Anna Herman-Czezuch, Nicola Kimiaie, Stefanie Meilinger, Christopher Schirrmeister, Hartwig Deneke, Jonas Witthuhn, and Felix Gödde
Adv. Sci. Res., 17, 165–173, https://doi.org/10.5194/asr-17-165-2020, https://doi.org/10.5194/asr-17-165-2020, 2020
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The power output of solar photovoltaic (PV) modules depends largely upon incident solar radiation as well as PV module temperature. Although irradiance can fluctuate rapidly under broken cloud conditions, module temperature is subject to latency due to the solar panel's heat capacity. In order to reconcile this difference a simple four-parameter model is successfully employed to describe the dynamics of PV module temperature as a function of atmospheric conditions.
Nicholas C. Parazoo, Troy Magney, Alex Norton, Brett Raczka, Cédric Bacour, Fabienne Maignan, Ian Baker, Yongguang Zhang, Bo Qiu, Mingjie Shi, Natasha MacBean, Dave R. Bowling, Sean P. Burns, Peter D. Blanken, Jochen Stutz, Katja Grossmann, and Christian Frankenberg
Biogeosciences, 17, 3733–3755, https://doi.org/10.5194/bg-17-3733-2020, https://doi.org/10.5194/bg-17-3733-2020, 2020
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Satellite measurements of solar-induced chlorophyll fluorescence (SIF) provide a global measure of photosynthetic change. This enables scientists to better track carbon cycle responses to environmental change and tune biochemical processes in vegetation models for an improved simulation of future change. We use tower-instrumented SIF measurements and controlled model experiments to assess the state of the art in terrestrial biosphere SIF modeling and find a wide range of sensitivities to light.
Susann Tegtmeier, Elliot Atlas, Birgit Quack, Franziska Ziska, and Kirstin Krüger
Atmos. Chem. Phys., 20, 7103–7123, https://doi.org/10.5194/acp-20-7103-2020, https://doi.org/10.5194/acp-20-7103-2020, 2020
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We investigate emissions of brominated gases from the ocean and their contribution to stratospheric ozone depletion. Once in the atmosphere, these gases usually break down in less than 6 months. Their impact on the ozone layer depends on the prevailing atmospheric circulation, since transport to the stratosphere requires uplift. We combine aircraft and ship observations with atmospheric modelling to analyse how, where, and when these gases are transported from the ocean into the stratosphere.
Jianzhong Ma, Steffen Dörner, Sebastian Donner, Junli Jin, Siyang Cheng, Junrang Guo, Zhanfeng Zhang, Jianqiong Wang, Peng Liu, Guoqing Zhang, Janis Pukite, Johannes Lampel, and Thomas Wagner
Atmos. Chem. Phys., 20, 6973–6990, https://doi.org/10.5194/acp-20-6973-2020, https://doi.org/10.5194/acp-20-6973-2020, 2020
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We made ground-based MAX-DOAS measurements at the Mt. Waliguan WMO GAW global baseline station (WLG) in the Tibetan Plateau during the years 2012–2015. We retrieve the differential slant column densities (dSCDs) of NO2, SO2, HCHO, and BrO from measured spectra at different elevation angles. Mixing ratios of these trace gases in the background troposphere over WLG are derived based on these dSCDs at a 1° elevation angle and the TRACY-2 radiative transfer model simulations.
Hans Brenna, Steffen Kutterolf, Michael J. Mills, and Kirstin Krüger
Atmos. Chem. Phys., 20, 6521–6539, https://doi.org/10.5194/acp-20-6521-2020, https://doi.org/10.5194/acp-20-6521-2020, 2020
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The Los Chocoyos supereruption (84 000 years ago) in Guatemala was one of the largest volcanic events of the last 100 000 years. This eruption released enormous amounts of sulfur, which cooled the climate, as well as chlorine and bromine, which destroyed the ozone in the stratosphere. We have simulated this eruption by using an advanced chemistry–climate model. We found a collapse in the ozone layer lasting more than 10 years, increased surface–UV radiation, and a 30-year climate-cooling period.
Karin Kreher, Michel Van Roozendael, Francois Hendrick, Arnoud Apituley, Ermioni Dimitropoulou, Udo Frieß, Andreas Richter, Thomas Wagner, Johannes Lampel, Nader Abuhassan, Li Ang, Monica Anguas, Alkis Bais, Nuria Benavent, Tim Bösch, Kristof Bognar, Alexander Borovski, Ilya Bruchkouski, Alexander Cede, Ka Lok Chan, Sebastian Donner, Theano Drosoglou, Caroline Fayt, Henning Finkenzeller, David Garcia-Nieto, Clio Gielen, Laura Gómez-Martín, Nan Hao, Bas Henzing, Jay R. Herman, Christian Hermans, Syedul Hoque, Hitoshi Irie, Junli Jin, Paul Johnston, Junaid Khayyam Butt, Fahim Khokhar, Theodore K. Koenig, Jonas Kuhn, Vinod Kumar, Cheng Liu, Jianzhong Ma, Alexis Merlaud, Abhishek K. Mishra, Moritz Müller, Monica Navarro-Comas, Mareike Ostendorf, Andrea Pazmino, Enno Peters, Gaia Pinardi, Manuel Pinharanda, Ankie Piters, Ulrich Platt, Oleg Postylyakov, Cristina Prados-Roman, Olga Puentedura, Richard Querel, Alfonso Saiz-Lopez, Anja Schönhardt, Stefan F. Schreier, André Seyler, Vinayak Sinha, Elena Spinei, Kimberly Strong, Frederik Tack, Xin Tian, Martin Tiefengraber, Jan-Lukas Tirpitz, Jeroen van Gent, Rainer Volkamer, Mihalis Vrekoussis, Shanshan Wang, Zhuoru Wang, Mark Wenig, Folkard Wittrock, Pinhua H. Xie, Jin Xu, Margarita Yela, Chengxin Zhang, and Xiaoyi Zhao
Atmos. Meas. Tech., 13, 2169–2208, https://doi.org/10.5194/amt-13-2169-2020, https://doi.org/10.5194/amt-13-2169-2020, 2020
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In September 2016, 36 spectrometers from 24 institutes measured a number of key atmospheric pollutants during an instrument intercomparison campaign (CINDI-2) at Cabauw, the Netherlands. Here we report on the outcome of this intercomparison exercise. The three major goals were to characterise the differences between the participating instruments, to define a robust methodology for performance assessment, and to contribute to the harmonisation of the measurement settings and retrieval methods.
Sinikka T. Lennartz, Christa A. Marandino, Marc von Hobe, Meinrat O. Andreae, Kazushi Aranami, Elliot Atlas, Max Berkelhammer, Heinz Bingemer, Dennis Booge, Gregory Cutter, Pau Cortes, Stefanie Kremser, Cliff S. Law, Andrew Marriner, Rafel Simó, Birgit Quack, Günther Uher, Huixiang Xie, and Xiaobin Xu
Earth Syst. Sci. Data, 12, 591–609, https://doi.org/10.5194/essd-12-591-2020, https://doi.org/10.5194/essd-12-591-2020, 2020
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Sulfur-containing trace gases in the atmosphere influence atmospheric chemistry and the energy budget of the Earth by forming aerosols. The ocean is an important source of the most abundant sulfur gas in the atmosphere, carbonyl sulfide (OCS) and its most important precursor carbon disulfide (CS2). In order to assess global variability of the sea surface concentrations of both gases to calculate their oceanic emissions, we have compiled a database of existing shipborne measurements.
Zoë Y. W. Davis, Udo Frieß, Kevin B. Strawbridge, Monika Aggarwaal, Sabour Baray, Elijah G. Schnitzler, Akshay Lobo, Vitali E. Fioletov, Ihab Abboud, Chris A. McLinden, Jim Whiteway, Megan D. Willis, Alex K. Y. Lee, Jeff Brook, Jason Olfert, Jason O'Brien, Ralf Staebler, Hans D. Osthoff, Cristian Mihele, and Robert McLaren
Atmos. Meas. Tech., 13, 1129–1155, https://doi.org/10.5194/amt-13-1129-2020, https://doi.org/10.5194/amt-13-1129-2020, 2020
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Here, we evaluate a ground-based remote sensing method (MAX-DOAS) for measuring total pollutant loading and vertical profiles of pollution in the lower atmosphere by comparing our method to a variety of other measurement methods (lidar, sunphotometer, active DOAS, and aircraft measurements). Measurements were made in the Athabasca Oil Sands Region in Alberta, Canada. The complex dataset provided a rare opportunity to evaluate the performance of MAX-DOAS under varying atmospheric conditions.
Sebastian Donner, Jonas Kuhn, Michel Van Roozendael, Alkiviadis Bais, Steffen Beirle, Tim Bösch, Kristof Bognar, Ilya Bruchkouski, Ka Lok Chan, Steffen Dörner, Theano Drosoglou, Caroline Fayt, Udo Frieß, François Hendrick, Christian Hermans, Junli Jin, Ang Li, Jianzhong Ma, Enno Peters, Gaia Pinardi, Andreas Richter, Stefan F. Schreier, André Seyler, Kimberly Strong, Jan-Lukas Tirpitz, Yang Wang, Pinhua Xie, Jin Xu, Xiaoyi Zhao, and Thomas Wagner
Atmos. Meas. Tech., 13, 685–712, https://doi.org/10.5194/amt-13-685-2020, https://doi.org/10.5194/amt-13-685-2020, 2020
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The calibration of the elevation angles of MAX-DOAS instruments is important for the correct interpretation of such MAX-DOAS measurements. We present and evaluate different methods for the elevation calibration of MAX-DOAS instruments which were applied during the CINDI-2 field campaign.
Susann Tegtmeier, James Anstey, Sean Davis, Rossana Dragani, Yayoi Harada, Ioana Ivanciu, Robin Pilch Kedzierski, Kirstin Krüger, Bernard Legras, Craig Long, James S. Wang, Krzysztof Wargan, and Jonathon S. Wright
Atmos. Chem. Phys., 20, 753–770, https://doi.org/10.5194/acp-20-753-2020, https://doi.org/10.5194/acp-20-753-2020, 2020
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The tropical tropopause layer is an important atmospheric region right in between the troposphere and the stratosphere. We evaluate the representation of this layer in reanalyses data sets, which create a complete picture of the state of Earth's atmosphere using atmospheric modeling and available observations. The recent reanalyses show realistic temperatures in the tropical tropopause layer. However, where the temperature is lowest, the so-called cold point, the reanalyses are too cold.
Ulrich Platt and Jonas Kuhn
Atmos. Meas. Tech., 12, 6259–6272, https://doi.org/10.5194/amt-12-6259-2019, https://doi.org/10.5194/amt-12-6259-2019, 2019
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Measurements of atmospheric trace gases by absorption spectroscopy are frequently supported by recording the amount of trace gas in absorption cells. These are typically small glass (or quartz) cylinders containing the gas to be studied. Here we show in the example of NO2-absorption cells that the effective amount of gas seen by the instrument can deviate greatly from expected values (by orders of magnitude in severe cases). Some suggestions for improving the situation are discussed.
Yue Jia, Susann Tegtmeier, Elliot Atlas, and Birgit Quack
Atmos. Chem. Phys., 19, 11089–11103, https://doi.org/10.5194/acp-19-11089-2019, https://doi.org/10.5194/acp-19-11089-2019, 2019
Ulrike Niemeier, Claudia Timmreck, and Kirstin Krüger
Atmos. Chem. Phys., 19, 10379–10390, https://doi.org/10.5194/acp-19-10379-2019, https://doi.org/10.5194/acp-19-10379-2019, 2019
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In 1963 Mt. Agung, Indonesia, showed unrest for several months. During this period,
two medium-sized eruptions injected SO2 into the stratosphere. Recent volcanic emission datasets include only one large eruption phase. Therefore, we compared model experiments, with (a) one larger eruption and (b) two eruptions as observed. The evolution of the volcanic cloud differs significantly between the two experiments. Both climatic eruptions should be taken into account.
Sinikka T. Lennartz, Marc von Hobe, Dennis Booge, Henry C. Bittig, Tim Fischer, Rafael Gonçalves-Araujo, Kerstin B. Ksionzek, Boris P. Koch, Astrid Bracher, Rüdiger Röttgers, Birgit Quack, and Christa A. Marandino
Ocean Sci., 15, 1071–1090, https://doi.org/10.5194/os-15-1071-2019, https://doi.org/10.5194/os-15-1071-2019, 2019
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The ocean emits the gases carbonyl sulfide (OCS) and carbon disulfide (CS2), which affect our climate. The goal of this study was to quantify the rates at which both gases are produced in the eastern tropical South Pacific (ETSP), one of the most productive oceanic regions worldwide. Both gases are produced by reactions triggered by sunlight, but we found that the amount produced depends on different factors. Our results improve numerical models to predict oceanic concentrations of both gases.
Maximilian Herrmann, Le Cao, Holger Sihler, Ulrich Platt, and Eva Gutheil
Atmos. Chem. Phys., 19, 10161–10190, https://doi.org/10.5194/acp-19-10161-2019, https://doi.org/10.5194/acp-19-10161-2019, 2019
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The oscillations of tropospheric ODEs in the Arctic spring is studied numerically. After the termination of an ODE, the reactive bromine is deposited onto aerosols/the snow surface, and the ozone may regenerate. The replenished ozone is available for the next autocatalytic bromine release, leading to the oscillation of an ODE. Its dependence on the NOx mixing ratio, the inversion layer strength, the ambient temperature, the aerosol density, and the solar radiation is investigated.
Jan-Marcus Nasse, Philipp G. Eger, Denis Pöhler, Stefan Schmitt, Udo Frieß, and Ulrich Platt
Atmos. Meas. Tech., 12, 4149–4169, https://doi.org/10.5194/amt-12-4149-2019, https://doi.org/10.5194/amt-12-4149-2019, 2019
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We present several changes to the setup of long-path differential optical absorption spectroscopy (LP-DOAS) instruments, including the application of a laser-driven light source, a modified coupling of the measurement signal between components, improved stray-light suppression, and better signal homogenization measures. These changes reduce detection limits of typical trace-gas species by a factor of 3–4 compared to previous setups and enable automated long-term observations in Antarctica.
Josefine Maas, Susann Tegtmeier, Birgit Quack, Arne Biastoch, Jonathan V. Durgadoo, Siren Rühs, Stephan Gollasch, and Matej David
Ocean Sci., 15, 891–904, https://doi.org/10.5194/os-15-891-2019, https://doi.org/10.5194/os-15-891-2019, 2019
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In a large-scale analysis, the spread of disinfection by-products from oxidative ballast water treatment is investigated, with a focus on Southeast Asia where major ports are located. Halogenated compounds such as bromoform (CHBr3) are produced in the ballast water and, once emitted into the environment, can participate in ozone depletion. Anthropogenic bromoform is rapidly emitted into the atmosphere and can locally double around large ports. A large-scale impact cannot be found.
Martin Horbanski, Denis Pöhler, Johannes Lampel, and Ulrich Platt
Atmos. Meas. Tech., 12, 3365–3381, https://doi.org/10.5194/amt-12-3365-2019, https://doi.org/10.5194/amt-12-3365-2019, 2019
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ICAD allows a precise in situ measurement of gases like NO2 in a relatively simple and compact setup. The main advantage in comparison to most other optical methods is that it does not require a stable total light intensity. This allows a simpler and mobile instrument setup and additionally it features no observed cross-interferences. We validated the high quality for an ICAD NO2 instrument in different inter-comparisons with a detection limit of 0.02 ppbv.
Florian Dinger, Stefan Bredemeyer, Santiago Arellano, Nicole Bobrowski, Ulrich Platt, and Thomas Wagner
Solid Earth, 10, 725–740, https://doi.org/10.5194/se-10-725-2019, https://doi.org/10.5194/se-10-725-2019, 2019
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Evidence for tidal impacts on volcanism have been gathered by numerous empirical studies. This paper elucidates whether a causal link from the tidal forces to a variation in the volcanic degassing can be traced analytically. We model the response of a simplified magmatic system to the local tidal gravity variations, find that the tide-induced dynamics may significantly alter the bubble coalescence rate, and discuss the consequences for volcanic degassing behaviour.
Thomas Wagner, Steffen Beirle, Nuria Benavent, Tim Bösch, Ka Lok Chan, Sebastian Donner, Steffen Dörner, Caroline Fayt, Udo Frieß, David García-Nieto, Clio Gielen, David González-Bartolome, Laura Gomez, François Hendrick, Bas Henzing, Jun Li Jin, Johannes Lampel, Jianzhong Ma, Kornelia Mies, Mónica Navarro, Enno Peters, Gaia Pinardi, Olga Puentedura, Janis Puķīte, Julia Remmers, Andreas Richter, Alfonso Saiz-Lopez, Reza Shaiganfar, Holger Sihler, Michel Van Roozendael, Yang Wang, and Margarita Yela
Atmos. Meas. Tech., 12, 2745–2817, https://doi.org/10.5194/amt-12-2745-2019, https://doi.org/10.5194/amt-12-2745-2019, 2019
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In this study the consistency between MAX-DOAS measurements and radiative transfer simulations of the atmospheric O4 absorption is investigated. The study is based on measurements (2 selected days during the MADCAT campaign) as well as synthetic spectra. The uncertainties of all relevant aspects (spectral retrieval and radiative transfer simulations) are quantified. For one of the selected days, measurements and simulations do not agree within their uncertainties.
Udo Frieß, Steffen Beirle, Leonardo Alvarado Bonilla, Tim Bösch, Martina M. Friedrich, François Hendrick, Ankie Piters, Andreas Richter, Michel van Roozendael, Vladimir V. Rozanov, Elena Spinei, Jan-Lukas Tirpitz, Tim Vlemmix, Thomas Wagner, and Yang Wang
Atmos. Meas. Tech., 12, 2155–2181, https://doi.org/10.5194/amt-12-2155-2019, https://doi.org/10.5194/amt-12-2155-2019, 2019
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Multi-axis differential optical absorption spectroscopy (MAX-DOAS) is a widely used measurement technique for the detection of a variety of atmospheric trace gases. It enables the retrieval of aerosol and trace gas vertical profiles in the atmospheric boundary layer using appropriate retrieval algorithms. In this study, the ability of eight profile retrieval algorithms to reconstruct vertical profiles is assessed on the basis of synthetic measurements.
Alba Badia, Claire E. Reeves, Alex R. Baker, Alfonso Saiz-Lopez, Rainer Volkamer, Theodore K. Koenig, Eric C. Apel, Rebecca S. Hornbrook, Lucy J. Carpenter, Stephen J. Andrews, Tomás Sherwen, and Roland von Glasow
Atmos. Chem. Phys., 19, 3161–3189, https://doi.org/10.5194/acp-19-3161-2019, https://doi.org/10.5194/acp-19-3161-2019, 2019
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The oceans have an impact on the composition and reactivity of the troposphere through the emission of gases and particles. Thus, a quantitative understanding of the marine atmosphere is crucial to examine the oxidative capacity and climate forcing. This study investigates the impact of halogens in the tropical troposphere and explores the sensitivity of this to uncertainties in the fluxes and their chemical processing. Our modelled tropospheric Ox loss due to halogens ranges from 20 % to 60 %.
Jonas Kuhn, Ulrich Platt, Nicole Bobrowski, and Thomas Wagner
Atmos. Meas. Tech., 12, 735–747, https://doi.org/10.5194/amt-12-735-2019, https://doi.org/10.5194/amt-12-735-2019, 2019
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We study a novel remote-sensing technique for atmospheric trace gases absorbing in the UV and visible spectral range. Using Fabry–Perot interferometers with a spectral transmission matched to the trace gas's spectral absorption allows for imaging trace gases with high sensitivity and selectivity. The thereby achieved high spatio-temporal resolution enables the study of small-scale and dynamic processes in the atmosphere. We present sample calculations and a proof-of-concept study.
Tim Bösch, Vladimir Rozanov, Andreas Richter, Enno Peters, Alexei Rozanov, Folkard Wittrock, Alexis Merlaud, Johannes Lampel, Stefan Schmitt, Marijn de Haij, Stijn Berkhout, Bas Henzing, Arnoud Apituley, Mirjam den Hoed, Jan Vonk, Martin Tiefengraber, Moritz Müller, and John Philip Burrows
Atmos. Meas. Tech., 11, 6833–6859, https://doi.org/10.5194/amt-11-6833-2018, https://doi.org/10.5194/amt-11-6833-2018, 2018
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A new MAX-DOAS profiling algorithm for aerosols and trace
gases was developed.
The performance of this novel algorithm was tested with the help of
synthetic data and measurements from the CINDI-2 campaign in Cabauw, the
Netherlands, in 2016.
Robert G. Ryan, Steve Rhodes, Matthew Tully, Stephen Wilson, Nicholas Jones, Udo Frieß, and Robyn Schofield
Atmos. Chem. Phys., 18, 13969–13985, https://doi.org/10.5194/acp-18-13969-2018, https://doi.org/10.5194/acp-18-13969-2018, 2018
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Nitrous acid (HONO) plays a crucial role in the self-cleansing capacity of the atmosphere but its formation mechanisms and spatial distributions are not well understood. This paper presents spectroscopic measurements of HONO, NO2 and aerosol measurements from Melbourne, Australia. HONO levels are at a maximum in the middle of the day, which is unprecedented for an urban area, and these measurements provide evidence for the existence of a strong ground-based, daytime nitrogen oxide source.
Alina Fiehn, Birgit Quack, Irene Stemmler, Franziska Ziska, and Kirstin Krüger
Atmos. Chem. Phys., 18, 11973–11990, https://doi.org/10.5194/acp-18-11973-2018, https://doi.org/10.5194/acp-18-11973-2018, 2018
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Oceanic very short-lived substances, VSLS, contribute to stratospheric halogen loading and ozone depletion. We created bromoform emission inventories with monthly resolution for the tropical Indian Ocean and west Pacific and modeled the atmospheric transport of bromoform with the particle dispersion model FLEXPART/ERA-Interim. Results underline that the seasonal and regional stratospheric bromine entrainment critically depends on the seasonality and spatial distribution of the VSLS emissions.
Stephen Broccardo, Klaus-Peter Heue, David Walter, Christian Meyer, Alexander Kokhanovsky, Ronald van der A, Stuart Piketh, Kristy Langerman, and Ulrich Platt
Atmos. Meas. Tech., 11, 2797–2819, https://doi.org/10.5194/amt-11-2797-2018, https://doi.org/10.5194/amt-11-2797-2018, 2018
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Measurements of nitrogen dioxide, known to originate from industrial and automotive combustion sources, have been made from space for two decades. Successive generations of instrument bring improvements in ground-pixel resolution; however features in the atmosphere are known to be smaller than what the satellites can resolve. Measurements of urban and industrial areas using a high-resolution airborne instrument allow the impact of the satellite's relatively low resolution to be evaluated.
David W. T. Griffith, Denis Pöhler, Stefan Schmitt, Samuel Hammer, Sanam N. Vardag, and Ulrich Platt
Atmos. Meas. Tech., 11, 1549–1563, https://doi.org/10.5194/amt-11-1549-2018, https://doi.org/10.5194/amt-11-1549-2018, 2018
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Measurements of atmospheric trace gases over an open path complement in situ measurements by spatial averaging. This paper describes the first open-path measurements of CO2, CH4 and other trace gases by near-infrared Fourier transform spectroscopy. The measurements were made in Heidelberg, Germany, for 4 months in 2014 over a 1.5 km path and compared to in situ measurements made at one end of the path. The experiment setup and methods (and the comparisons of open path to in situ) are described.
Steffen Beirle, Johannes Lampel, Yang Wang, Kornelia Mies, Steffen Dörner, Margherita Grossi, Diego Loyola, Angelika Dehn, Anja Danielczok, Marc Schröder, and Thomas Wagner
Earth Syst. Sci. Data, 10, 449–468, https://doi.org/10.5194/essd-10-449-2018, https://doi.org/10.5194/essd-10-449-2018, 2018
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We present time series of the global distribution of water vapor over more than 2 decades based on satellite measurements from different sensors. A particular focus is the consistency amongst the different sensors to avoid jumps from one instrument to another. This is reached by applying robust and simple retrieval settings consistently. The resulting
Climateproduct allows the study of the temporal evolution of water vapor over the last 20 years on a global scale.
Florian Dinger, Nicole Bobrowski, Simon Warnach, Stefan Bredemeyer, Silvana Hidalgo, Santiago Arellano, Bo Galle, Ulrich Platt, and Thomas Wagner
Solid Earth, 9, 247–266, https://doi.org/10.5194/se-9-247-2018, https://doi.org/10.5194/se-9-247-2018, 2018
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We monitored the bromine monoxide-to-sulfur dioxide molar ratio in the effusive gas plume of Cotopaxi volcano in order to gain insight into the geological processes which control the pressure regime of the volcanic system. We observed a conspicuous periodic pattern with a periodicity of about 2 weeks, which significantly correlates with the Earth tidal forcing. Our results support a possible Earth tidal impact on volcanic activity, in particular for the Cotopaxi eruption 2015.
Christoph Kleinschmitt, Olivier Boucher, and Ulrich Platt
Atmos. Chem. Phys., 18, 2769–2786, https://doi.org/10.5194/acp-18-2769-2018, https://doi.org/10.5194/acp-18-2769-2018, 2018
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We use a state-of-the-art stratospheric aerosol model to study geoengineering through stratospheric sulfur injections. We find that the efficiency may decrease more drastically for larger injections than previously estimated and that injections at higher altitude are not more effective. This study may provide additional evidence that this proposed geoengineering technique is still more complicated, probably less effective, and may implicate stronger side effects than initially thought.
Johannes Lampel, Johannes Zielcke, Stefan Schmitt, Denis Pöhler, Udo Frieß, Ulrich Platt, and Thomas Wagner
Atmos. Chem. Phys., 18, 1671–1683, https://doi.org/10.5194/acp-18-1671-2018, https://doi.org/10.5194/acp-18-1671-2018, 2018
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Previous publications on the absorptions of the oxygen dimer O2–O2 (or short: O4) list absorption peaks at 328 nm and 419 nm, for which no spectrally resolved literature cross sections are available. As these absorptions potentially influence the spectral retrieval of various other trace gases, their shape and magnitude need to be quantified. We approximate the absorption peaks at 328 nm and 419 nm by their respective neighboring absorption peaks to estimate their magnitude and peak wavelength.
Johannes Lampel, Yang Wang, Andreas Hilboll, Steffen Beirle, Holger Sihler, Janis Puķīte, Ulrich Platt, and Thomas Wagner
Atmos. Meas. Tech., 10, 4819–4831, https://doi.org/10.5194/amt-10-4819-2017, https://doi.org/10.5194/amt-10-4819-2017, 2017
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Experience of differential atmospheric absorption spectroscopy (DOAS) shows that a spectral shift between measurement and reference spectrum is frequently required in order to achieve optimal fit results. The shift is often attributed to temporal instabilities of the instrument but implicitly solved the problem of the tilt effect discussed in this paper. The tilt effect results from the finite resolution of the measurements and amounts to 2 pm for the example data set.
Tilman Hüneke, Oliver-Alex Aderhold, Jannik Bounin, Marcel Dorf, Eric Gentry, Katja Grossmann, Jens-Uwe Grooß, Peter Hoor, Patrick Jöckel, Mareike Kenntner, Marvin Knapp, Matthias Knecht, Dominique Lörks, Sabrina Ludmann, Sigrun Matthes, Rasmus Raecke, Marcel Reichert, Jannis Weimar, Bodo Werner, Andreas Zahn, Helmut Ziereis, and Klaus Pfeilsticker
Atmos. Meas. Tech., 10, 4209–4234, https://doi.org/10.5194/amt-10-4209-2017, https://doi.org/10.5194/amt-10-4209-2017, 2017
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This paper describes a novel instrument for the aircraft-borne remote sensing of trace gases and liquid and solid water. Until recently, such measurements could only be evaluated under clear-sky conditions. We present a characterization and error assessment of the novel "scaling method", which allows for the retrieval of absolute trace gas concentrations under all sky conditions, significantly expanding the applicability of such measurements to study atmospheric photochemistry.
Yang Wang, Steffen Beirle, Francois Hendrick, Andreas Hilboll, Junli Jin, Aleksandra A. Kyuberis, Johannes Lampel, Ang Li, Yuhan Luo, Lorenzo Lodi, Jianzhong Ma, Monica Navarro, Ivan Ortega, Enno Peters, Oleg L. Polyansky, Julia Remmers, Andreas Richter, Olga Puentedura, Michel Van Roozendael, André Seyler, Jonathan Tennyson, Rainer Volkamer, Pinhua Xie, Nikolai F. Zobov, and Thomas Wagner
Atmos. Meas. Tech., 10, 3719–3742, https://doi.org/10.5194/amt-10-3719-2017, https://doi.org/10.5194/amt-10-3719-2017, 2017
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Slant column densities of nitrous acid (HONO) derived from different MAX-DOAS instruments and retrieval software are systematically compared for the first time during the Multi Axis DOAS – Comparison campaign for Aerosols and Trace gases (MAD-CAT) campaign held at MPIC in Mainz, Germany, from June to October 2013. Through the inter-comparisons and sensitivity studies we quantified the uncertainties in the DOAS fits of HONO from different sources and concluded a recommended setting.
Cathleen Schlundt, Susann Tegtmeier, Sinikka T. Lennartz, Astrid Bracher, Wee Cheah, Kirstin Krüger, Birgit Quack, and Christa A. Marandino
Atmos. Chem. Phys., 17, 10837–10854, https://doi.org/10.5194/acp-17-10837-2017, https://doi.org/10.5194/acp-17-10837-2017, 2017
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For the first time, oxygenated volatile organic carbon (OVOC) in the ocean and overlaying atmosphere in the western Pacific Ocean has been measured. OVOCs are important for atmospheric chemistry. They are involved in ozone production in the upper troposphere (UT), and they have a climate cooling effect. We showed that phytoplankton was an important source for OVOCs in the surface ocean, and when OVOCs are emitted into the atmosphere, they could reach the UT and might influence ozone formation.
Christoph Kleinschmitt, Olivier Boucher, Slimane Bekki, François Lott, and Ulrich Platt
Geosci. Model Dev., 10, 3359–3378, https://doi.org/10.5194/gmd-10-3359-2017, https://doi.org/10.5194/gmd-10-3359-2017, 2017
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Stratospheric aerosols play an important role in the climate system by affecting the Earth's radiative budget. In this article we present the newly developed LMDZ-S3A model and assess its performance against observations in periods of low and high aerosol loading. The model may serve as a tool to study the climate impacts of volcanic eruptions, as well as the deliberate injection of aerosols into the stratosphere, which has been proposed as a method of geoengineering to abate global warming.
William R. Simpson, Peter K. Peterson, Udo Frieß, Holger Sihler, Johannes Lampel, Ulrich Platt, Chris Moore, Kerri Pratt, Paul Shepson, John Halfacre, and Son V. Nghiem
Atmos. Chem. Phys., 17, 9291–9309, https://doi.org/10.5194/acp-17-9291-2017, https://doi.org/10.5194/acp-17-9291-2017, 2017
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We investigated Arctic atmospheric bromine chemistry during March–April 2012 to improve understanding of the role of sea ice and cracks in sea ice (leads) in this phenomenon. We find that leads vertically redistribute reactive bromine but that open/re-freezing leads are not major direct reactive halogen sources. Surface ozone depletion affects the vertical distribution and amount of reactive halogens, and aerosol particles are necessary but not sufficient to maintain reactive bromine aloft.
Peter K. Peterson, Denis Pöhler, Holger Sihler, Johannes Zielcke, Stephan General, Udo Frieß, Ulrich Platt, William R. Simpson, Son V. Nghiem, Paul B. Shepson, Brian H. Stirm, Suresh Dhaniyala, Thomas Wagner, Dana R. Caulton, Jose D. Fuentes, and Kerri A. Pratt
Atmos. Chem. Phys., 17, 7567–7579, https://doi.org/10.5194/acp-17-7567-2017, https://doi.org/10.5194/acp-17-7567-2017, 2017
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High-spatial-resolution aircraft measurements in the Arctic showed the sustained transport of reactive bromine in a lofted layer via heterogeneous reactions on aerosol particles. This process provides an explanation for free tropospheric reactive bromine and the significant spatial extent of satellite-observed bromine monoxide. The knowledge gained herein improves our understanding of the fate and transport of atmospheric pollutants in the Arctic.
Alina Fiehn, Birgit Quack, Helmke Hepach, Steffen Fuhlbrügge, Susann Tegtmeier, Matthew Toohey, Elliot Atlas, and Kirstin Krüger
Atmos. Chem. Phys., 17, 6723–6741, https://doi.org/10.5194/acp-17-6723-2017, https://doi.org/10.5194/acp-17-6723-2017, 2017
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Halogenated very short-lived substances (VSLSs) are naturally produced in the ocean and emitted to the atmosphere. In the stratosphere, these compounds can have a significant influence on the ozone layer and climate. During a research cruise in the west Indian Ocean, we found an important source region of halogenated VSLSs during the Asian summer monsoon. Modeling the transport from the ocean to the stratosphere we found two main pathways, one over the Indian Ocean and one over northern India.
Yang Wang, Steffen Beirle, Johannes Lampel, Mariliza Koukouli, Isabelle De Smedt, Nicolas Theys, Ang Li, Dexia Wu, Pinhua Xie, Cheng Liu, Michel Van Roozendael, Trissevgeni Stavrakou, Jean-François Müller, and Thomas Wagner
Atmos. Chem. Phys., 17, 5007–5033, https://doi.org/10.5194/acp-17-5007-2017, https://doi.org/10.5194/acp-17-5007-2017, 2017
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A long-term MAX-DOAS measurement from 2011 to 2014 was operated in Wuxi, part of the most industrialized area of the Yangtze River delta region of China. The tropospheric VCDs and vertical profiles of NO2, SO2 and HCHO derived from the MAX-DOAS are used to validate the products derived from OMI and GOME-2A/B by different scientific teams (daily- and bimonthly-averaged data). We investigate the effects of clouds, aerosols and a priori profile shapes on satellite retrievals of tropospheric VCDs.
Kevin Wolf, André Ehrlich, Tilman Hüneke, Klaus Pfeilsticker, Frank Werner, Martin Wirth, and Manfred Wendisch
Atmos. Chem. Phys., 17, 4283–4303, https://doi.org/10.5194/acp-17-4283-2017, https://doi.org/10.5194/acp-17-4283-2017, 2017
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The potential of airborne radiance measurements in the sideward and nadir directions for cirrus remote sensing is investigated. Therefore radiative transfer simulations were used and the sensitivity of upward radiance with respect to optical thickness, effective radius, surface albedo, wavelength and viewing angle was studied. It was shown that sideward observations lead to more accurate retrieval results. Investigating a case study of ML-CIRRUS, these findings are confirmed.
Christopher E. Sioris, Landon A. Rieger, Nicholas D. Lloyd, Adam E. Bourassa, Chris Z. Roth, Douglas A. Degenstein, Claude Camy-Peyret, Klaus Pfeilsticker, Gwenaël Berthet, Valéry Catoire, Florence Goutail, Jean-Pierre Pommereau, and Chris A. McLinden
Atmos. Meas. Tech., 10, 1155–1168, https://doi.org/10.5194/amt-10-1155-2017, https://doi.org/10.5194/amt-10-1155-2017, 2017
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A new OSIRIS NO2 retrieval algorithm is described and validated using > 40 balloon-based profile measurements. The validation results indicate a slight improvement relative to the existing operational algorithm in terms of the bias versus the balloon data, particularly in the lower stratosphere. The implication is that this new algorithm should replace the operational one. The motivation was to combine spectral fitting and the SaskTRAN radiative transfer model to achieve an improved product.
Jochen Stutz, Bodo Werner, Max Spolaor, Lisa Scalone, James Festa, Catalina Tsai, Ross Cheung, Santo F. Colosimo, Ugo Tricoli, Rasmus Raecke, Ryan Hossaini, Martyn P. Chipperfield, Wuhu Feng, Ru-Shan Gao, Eric J. Hintsa, James W. Elkins, Fred L. Moore, Bruce Daube, Jasna Pittman, Steven Wofsy, and Klaus Pfeilsticker
Atmos. Meas. Tech., 10, 1017–1042, https://doi.org/10.5194/amt-10-1017-2017, https://doi.org/10.5194/amt-10-1017-2017, 2017
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A new limb-scanning Differential Optical Absorption Spectroscopy (DOAS) instrument was developed for NASA’s Global Hawk unmanned aerial system during the Airborne Tropical TRopopause EXperiment to study trace gases in the tropical tropopause layer. A new technique that uses in situ and DOAS O3 observations together with radiative transfer calculations allows the retrieval of mixing ratios from the slant column densities of BrO and NO2 at high accuracies of 0.5 ppt and 15 ppt, respectively.
Angelika Klein, Peter Lübcke, Nicole Bobrowski, Jonas Kuhn, and Ulrich Platt
Atmos. Meas. Tech., 10, 979–987, https://doi.org/10.5194/amt-10-979-2017, https://doi.org/10.5194/amt-10-979-2017, 2017
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While measuring sulfur dioxide fluxes in volcanic plumes with a UV-sensitive camera, the wind direction can influence the retrieved fluxes. If the volcanic plume is tilted in the field of view of the camera, it can lead to over- or underestimations of the determined fluxes. This paper presents a method to deal with such a circumstance. Additionally, it provides the possibility to determine the wind direction of the plume directly from the image time series themselves.
Enno Peters, Gaia Pinardi, André Seyler, Andreas Richter, Folkard Wittrock, Tim Bösch, Michel Van Roozendael, François Hendrick, Theano Drosoglou, Alkiviadis F. Bais, Yugo Kanaya, Xiaoyi Zhao, Kimberly Strong, Johannes Lampel, Rainer Volkamer, Theodore Koenig, Ivan Ortega, Olga Puentedura, Mónica Navarro-Comas, Laura Gómez, Margarita Yela González, Ankie Piters, Julia Remmers, Yang Wang, Thomas Wagner, Shanshan Wang, Alfonso Saiz-Lopez, David García-Nieto, Carlos A. Cuevas, Nuria Benavent, Richard Querel, Paul Johnston, Oleg Postylyakov, Alexander Borovski, Alexander Elokhov, Ilya Bruchkouski, Haoran Liu, Cheng Liu, Qianqian Hong, Claudia Rivera, Michel Grutter, Wolfgang Stremme, M. Fahim Khokhar, Junaid Khayyam, and John P. Burrows
Atmos. Meas. Tech., 10, 955–978, https://doi.org/10.5194/amt-10-955-2017, https://doi.org/10.5194/amt-10-955-2017, 2017
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This work is about harmonization of differential optical absorption spectroscopy retrieval codes, which is a remote sensing technique widely used to derive atmospheric trace gas amounts. The study is based on ground-based measurements performed during the Multi-Axis DOAS Comparison campaign for Aerosols and Trace gases (MAD-CAT) in Mainz, Germany, in summer 2013. In total, 17 international groups working in the field of the DOAS technique participated in this study.
Holger Sihler, Peter Lübcke, Rüdiger Lang, Steffen Beirle, Martin de Graaf, Christoph Hörmann, Johannes Lampel, Marloes Penning de Vries, Julia Remmers, Ed Trollope, Yang Wang, and Thomas Wagner
Atmos. Meas. Tech., 10, 881–903, https://doi.org/10.5194/amt-10-881-2017, https://doi.org/10.5194/amt-10-881-2017, 2017
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This paper presents the independent and simple IFR method to retrieve the FOV of an instrument, i.e. the two-dimensional sensitivity distribution. IFR relies on correlated measurements featuring a higher spatial resolution and was applied to two satellite instruments, GOME-2 and OMI, and a DOAS instrument integrated in an SO2 camera. Our results confirm the commonly applied FOV distributions. IFR is applicable for verification exercises as well as degradation monitoring in the field.
Steffen Beirle, Johannes Lampel, Christophe Lerot, Holger Sihler, and Thomas Wagner
Atmos. Meas. Tech., 10, 581–598, https://doi.org/10.5194/amt-10-581-2017, https://doi.org/10.5194/amt-10-581-2017, 2017
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We propose to parameterize the instrumental spectral response function (ISRF) as a "super-Gaussian", which can reproduce a variety of shapes, from point-hat to boxcar shape, by just adding one parameter to the "classical" Gaussian.
In addition, the super-Gaussian allows for a straightforward parametrization of the effect of ISRF changes.
Gwenaël Berthet, Fabrice Jégou, Valéry Catoire, Gisèle Krysztofiak, Jean-Baptiste Renard, Adam E. Bourassa, Doug A. Degenstein, Colette Brogniez, Marcel Dorf, Sebastian Kreycy, Klaus Pfeilsticker, Bodo Werner, Franck Lefèvre, Tjarda J. Roberts, Thibaut Lurton, Damien Vignelles, Nelson Bègue, Quentin Bourgeois, Daniel Daugeron, Michel Chartier, Claude Robert, Bertrand Gaubicher, and Christophe Guimbaud
Atmos. Chem. Phys., 17, 2229–2253, https://doi.org/10.5194/acp-17-2229-2017, https://doi.org/10.5194/acp-17-2229-2017, 2017
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Since the last major volcanic event, i.e. the Pinatubo eruption in 1991, only
moderateeruptions have regularly injected sulfur into the stratosphere, typically enhancing the aerosol loading for several months. We investigate here for the first time the chemical perturbation associated with the Sarychev eruption in June 2009, using balloon-borne instruments and model calculations. Some chemical compounds are significantly affected by the aerosols, but the impact on stratospheric ozone is weak.
Yang Wang, Johannes Lampel, Pinhua Xie, Steffen Beirle, Ang Li, Dexia Wu, and Thomas Wagner
Atmos. Chem. Phys., 17, 2189–2215, https://doi.org/10.5194/acp-17-2189-2017, https://doi.org/10.5194/acp-17-2189-2017, 2017
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The air pollution in the Yangtze River delta (YRD), the largest economic region in China, threatens the health of the inhabitants in this region. A long-term MAX-DOAS observation in Wuxi, China (belonging to YRD), is used to characterize vertical distributions (VD) of the aerosols and the precursor trace gases in the boundary to identify the dominating sources. The results are valuable for further validation of satellite products and chemical transport modelings.
Nga Lee Ng, Steven S. Brown, Alexander T. Archibald, Elliot Atlas, Ronald C. Cohen, John N. Crowley, Douglas A. Day, Neil M. Donahue, Juliane L. Fry, Hendrik Fuchs, Robert J. Griffin, Marcelo I. Guzman, Hartmut Herrmann, Alma Hodzic, Yoshiteru Iinuma, José L. Jimenez, Astrid Kiendler-Scharr, Ben H. Lee, Deborah J. Luecken, Jingqiu Mao, Robert McLaren, Anke Mutzel, Hans D. Osthoff, Bin Ouyang, Benedicte Picquet-Varrault, Ulrich Platt, Havala O. T. Pye, Yinon Rudich, Rebecca H. Schwantes, Manabu Shiraiwa, Jochen Stutz, Joel A. Thornton, Andreas Tilgner, Brent J. Williams, and Rahul A. Zaveri
Atmos. Chem. Phys., 17, 2103–2162, https://doi.org/10.5194/acp-17-2103-2017, https://doi.org/10.5194/acp-17-2103-2017, 2017
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Oxidation of biogenic volatile organic compounds by NO3 is an important interaction between anthropogenic
and natural emissions. This review results from a June 2015 workshop and includes the recent literature
on kinetics, mechanisms, organic aerosol yields, and heterogeneous chemistry; advances in analytical
instrumentation; the current state NO3-BVOC chemistry in atmospheric models; and critical needs for
future research in modeling, field observations, and laboratory studies.
Masatomo Fujiwara, Jonathon S. Wright, Gloria L. Manney, Lesley J. Gray, James Anstey, Thomas Birner, Sean Davis, Edwin P. Gerber, V. Lynn Harvey, Michaela I. Hegglin, Cameron R. Homeyer, John A. Knox, Kirstin Krüger, Alyn Lambert, Craig S. Long, Patrick Martineau, Andrea Molod, Beatriz M. Monge-Sanz, Michelle L. Santee, Susann Tegtmeier, Simon Chabrillat, David G. H. Tan, David R. Jackson, Saroja Polavarapu, Gilbert P. Compo, Rossana Dragani, Wesley Ebisuzaki, Yayoi Harada, Chiaki Kobayashi, Will McCarty, Kazutoshi Onogi, Steven Pawson, Adrian Simmons, Krzysztof Wargan, Jeffrey S. Whitaker, and Cheng-Zhi Zou
Atmos. Chem. Phys., 17, 1417–1452, https://doi.org/10.5194/acp-17-1417-2017, https://doi.org/10.5194/acp-17-1417-2017, 2017
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We introduce the SPARC Reanalysis Intercomparison Project (S-RIP), review key concepts and elements of atmospheric reanalysis systems, and summarize the technical details of and differences among 11 of these systems. This work supports scientific studies and intercomparisons of reanalysis products by collecting these background materials and technical details into a single reference. We also address several common misunderstandings and points of confusion regarding reanalyses.
Johannes Lampel, Denis Pöhler, Oleg L. Polyansky, Aleksandra A. Kyuberis, Nikolai F. Zobov, Jonathan Tennyson, Lorenzo Lodi, Udo Frieß, Yang Wang, Steffen Beirle, Ulrich Platt, and Thomas Wagner
Atmos. Chem. Phys., 17, 1271–1295, https://doi.org/10.5194/acp-17-1271-2017, https://doi.org/10.5194/acp-17-1271-2017, 2017
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Water vapour is known to absorb radiation from the microwave region to the blue part of the visible spectrum.
Ab initio approaches to model individual absorption lines of the gaseous water molecule predict absorption lines
until its dissociation limit at 243 nm.
We present first evidence of water vapour absorption near 363 nm from field measurements using data
from multi-axis differential optical absorption spectroscopy (MAX-DOAS) and long-path (LP)-DOAS measurements.
Bodo Werner, Jochen Stutz, Max Spolaor, Lisa Scalone, Rasmus Raecke, James Festa, Santo Fedele Colosimo, Ross Cheung, Catalina Tsai, Ryan Hossaini, Martyn P. Chipperfield, Giorgio S. Taverna, Wuhu Feng, James W. Elkins, David W. Fahey, Ru-Shan Gao, Erik J. Hintsa, Troy D. Thornberry, Free Lee Moore, Maria A. Navarro, Elliot Atlas, Bruce C. Daube, Jasna Pittman, Steve Wofsy, and Klaus Pfeilsticker
Atmos. Chem. Phys., 17, 1161–1186, https://doi.org/10.5194/acp-17-1161-2017, https://doi.org/10.5194/acp-17-1161-2017, 2017
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The paper reports on inorganic and organic bromine measured in the tropical tropopause layer (TTL) over the eastern Pacific in early 2013. Bryinorg is found to increase from a mean of 2.63 ± 1.04 ppt for θ in the range of 350–360 K to 5.11 ± 1.57 ppt for θ=390 ± 400 K, whereas in the subtropical lower stratosphere, it reaches 7.66 ± 2.95 ppt for θ in the range of 390–400 K. Within the TTL, total bromine is found to range from 20.3 ppt to 22.3 ppt.
Sinikka T. Lennartz, Christa A. Marandino, Marc von Hobe, Pau Cortes, Birgit Quack, Rafel Simo, Dennis Booge, Andrea Pozzer, Tobias Steinhoff, Damian L. Arevalo-Martinez, Corinna Kloss, Astrid Bracher, Rüdiger Röttgers, Elliot Atlas, and Kirstin Krüger
Atmos. Chem. Phys., 17, 385–402, https://doi.org/10.5194/acp-17-385-2017, https://doi.org/10.5194/acp-17-385-2017, 2017
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We present new sea surface and marine boundary layer measurements of carbonyl sulfide, the most abundant sulfur gas in the atmosphere, and calculate an oceanic emission estimate. Our results imply that oceanic emissions are very unlikely to account for the missing source in the atmospheric budget that is currently discussed for OCS.
Peter Lübcke, Johannes Lampel, Santiago Arellano, Nicole Bobrowski, Florian Dinger, Bo Galle, Gustavo Garzón, Silvana Hidalgo, Zoraida Chacón Ortiz, Leif Vogel, Simon Warnach, and Ulrich Platt
Atmos. Meas. Tech., 9, 5677–5698, https://doi.org/10.5194/amt-9-5677-2016, https://doi.org/10.5194/amt-9-5677-2016, 2016
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We evaluated spectra from a scanning spectrometer network for the monitoring of volcanic gas emissions using a modelled background spectrum. Statistical methods were applied in order to improve the quality of the spectroscopic evaluation. We used this technique to assess the robustness of standard retrievals at two volcanos: Nevado del Ruiz (Colombia) and Tungurahua (Ecuador).
Christoph Hörmann, Holger Sihler, Steffen Beirle, Marloes Penning de Vries, Ulrich Platt, and Thomas Wagner
Atmos. Chem. Phys., 16, 13015–13034, https://doi.org/10.5194/acp-16-13015-2016, https://doi.org/10.5194/acp-16-13015-2016, 2016
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We present 10 years of bromine monoxide (BrO) satellite observations by the Ozone Monitoring Instrument (OMI) over the Rann of Kutch salt marsh. The measurements reveal a typical seasonal cycle of BrO with maximum concentrations during April/May. The results indicate that the Rann of Kutch is probably one of the strongest natural point sources of reactive bromine compounds outside the polar regions and is thought to have a significant impact on local and regional ozone chemistry.
Shanshan Wang, Carlos A. Cuevas, Udo Frieß, and Alfonso Saiz-Lopez
Atmos. Meas. Tech., 9, 5089–5101, https://doi.org/10.5194/amt-9-5089-2016, https://doi.org/10.5194/amt-9-5089-2016, 2016
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Multi-axis differential optical absorption spectroscopy (MAX-DOAS) measurements were performed in the urban environment of Madrid, Spain, where Sahara dust intrusion sometimes occurs. The study shows a high performances in the retrieval of aerosol optical depth, the surface extinction coefficient and an elevated layer during dust episodes, validated by AERONET in situ and modeling data. It is essential to capture the extinction properties of both local aerosol and Saharan dust.
Steffen Fuhlbrügge, Birgit Quack, Elliot Atlas, Alina Fiehn, Helmke Hepach, and Kirstin Krüger
Atmos. Chem. Phys., 16, 12205–12217, https://doi.org/10.5194/acp-16-12205-2016, https://doi.org/10.5194/acp-16-12205-2016, 2016
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This study presents novel observations of the very short lived substances (VSLSs) bromoform, dibromomethane and methyl iodide with high-resolution meteorological measurements and Lagrangian transport in the Peruvian upwelling. With a simple source–loss estimate we identified VSLS abundances below the trade inversion to be significantly influenced by advection of regional sources, underscoring the importance of oceanic upwelling and trade winds on the atmospheric distribution of VSLS emission.
Helmke Hepach, Birgit Quack, Susann Tegtmeier, Anja Engel, Astrid Bracher, Steffen Fuhlbrügge, Luisa Galgani, Elliot L. Atlas, Johannes Lampel, Udo Frieß, and Kirstin Krüger
Atmos. Chem. Phys., 16, 12219–12237, https://doi.org/10.5194/acp-16-12219-2016, https://doi.org/10.5194/acp-16-12219-2016, 2016
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We present surface seawater measurements of bromo- and iodocarbons, which are involved in numerous atmospheric processes such as tropospheric and stratospheric ozone chemistry, from the highly productive Peruvian upwelling. By combining trace gas measurements, characterization of organic matter and phytoplankton species, and tropospheric modelling, we show that large amounts of iodocarbons produced from the pool of organic matter may contribute strongly to local tropospheric iodine loading.
Tomás Sherwen, Johan A. Schmidt, Mat J. Evans, Lucy J. Carpenter, Katja Großmann, Sebastian D. Eastham, Daniel J. Jacob, Barbara Dix, Theodore K. Koenig, Roman Sinreich, Ivan Ortega, Rainer Volkamer, Alfonso Saiz-Lopez, Cristina Prados-Roman, Anoop S. Mahajan, and Carlos Ordóñez
Atmos. Chem. Phys., 16, 12239–12271, https://doi.org/10.5194/acp-16-12239-2016, https://doi.org/10.5194/acp-16-12239-2016, 2016
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We present a simulation of tropospheric Cl, Br, I chemistry within the GEOS-Chem CTM. We find a decrease in tropospheric ozone burden of 18.6 % and a 8.2 % decrease in global mean OH concentrations. Cl oxidation of some VOCs range from 15 to 27 % of the total loss. Bromine plays a small role in oxidising oVOCs. Surface ozone, ozone sondes, and methane lifetime are in general improved by the inclusion of halogens. We argue that simulated bromine and chlorine represent a lower limit.
Erna Frins, Reza Shaiganfar, Ulrich Platt, and Thomas Wagner
Atmos. Meas. Tech. Discuss., https://doi.org/10.5194/amt-2016-255, https://doi.org/10.5194/amt-2016-255, 2016
Revised manuscript has not been submitted
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Standard methods like in-situ measurements can hardly register NOx (= NO + NO2) emissions from aircrafts during take-off, when engines run at high load and thus an important amount of fuel is consumed and most of the harmful emissions are produced . The goal of this work is to show that it is possible to measure aircraft emissions generated during take-off (and initial part of the climb) by a remote spectroscopic method like automobile – based – Differential Optical Absorption Spectroscopy (DOAS).
R. Hossaini, P. K. Patra, A. A. Leeson, G. Krysztofiak, N. L. Abraham, S. J. Andrews, A. T. Archibald, J. Aschmann, E. L. Atlas, D. A. Belikov, H. Bönisch, L. J. Carpenter, S. Dhomse, M. Dorf, A. Engel, W. Feng, S. Fuhlbrügge, P. T. Griffiths, N. R. P. Harris, R. Hommel, T. Keber, K. Krüger, S. T. Lennartz, S. Maksyutov, H. Mantle, G. P. Mills, B. Miller, S. A. Montzka, F. Moore, M. A. Navarro, D. E. Oram, K. Pfeilsticker, J. A. Pyle, B. Quack, A. D. Robinson, E. Saikawa, A. Saiz-Lopez, S. Sala, B.-M. Sinnhuber, S. Taguchi, S. Tegtmeier, R. T. Lidster, C. Wilson, and F. Ziska
Atmos. Chem. Phys., 16, 9163–9187, https://doi.org/10.5194/acp-16-9163-2016, https://doi.org/10.5194/acp-16-9163-2016, 2016
U. Frieß, H. Klein Baltink, S. Beirle, K. Clémer, F. Hendrick, B. Henzing, H. Irie, G. de Leeuw, A. Li, M. M. Moerman, M. van Roozendael, R. Shaiganfar, T. Wagner, Y. Wang, P. Xie, S. Yilmaz, and P. Zieger
Atmos. Meas. Tech., 9, 3205–3222, https://doi.org/10.5194/amt-9-3205-2016, https://doi.org/10.5194/amt-9-3205-2016, 2016
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This article describes the first direct comparison of aerosol extinction profiles from Multi-Axis DOAS measurements of the oxygen collision complex using five different retrieval algorithms. A comparison of the retrieved profiles with co-located aerosol measurements shows good agreement with respect to profile shape and aerosol optical thickness. This study shows that MAX-DOAS is a simple, versatile and cost-effective method for the measurement of aerosol properties in the lower troposphere.
Le Cao, Ulrich Platt, Chenggang Wang, Nianwen Cao, and Qing Qin
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2016-553, https://doi.org/10.5194/acp-2016-553, 2016
Revised manuscript has not been submitted
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A snowpack module which represents the mass transfer between the ambient air and the snowpack is implemented in a box model, aiming to clarify the influences of the snowpack on the ozone depletion events (ODEs) and the associated bromine explosion in the springtime of Arctic. The size of snow grains, volume fraction of the liquid-like layer (LLL), and the rate of the mass exchange between the snow interstitial air and the snow particles are shown to be critical parameters.
Steffen Fuhlbrügge, Birgit Quack, Susann Tegtmeier, Elliot Atlas, Helmke Hepach, Qiang Shi, Stefan Raimund, and Kirstin Krüger
Atmos. Chem. Phys., 16, 7569–7585, https://doi.org/10.5194/acp-16-7569-2016, https://doi.org/10.5194/acp-16-7569-2016, 2016
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This study presents a novel estimate for the contribution of oceanic VSLS emissions to the atmospheric boundary layer and free troposphere during the SHIVA-Sonne cruise in the South China and Sulu seas in 2011. While oceanic emissions of CHBr3 and CH3I showed a significant contribution to their atmospheric abundances, atmospheric CH2Br2 appeared to be largely advected. Convective activity in the region can furthermore lead to low VSLS boundary layer mixing ratios despite high oceanic emissions.
N. Sobanski, M. J. Tang, J. Thieser, G. Schuster, D. Pöhler, H. Fischer, W. Song, C. Sauvage, J. Williams, J. Fachinger, F. Berkes, P. Hoor, U. Platt, J. Lelieveld, and J. N. Crowley
Atmos. Chem. Phys., 16, 4867–4883, https://doi.org/10.5194/acp-16-4867-2016, https://doi.org/10.5194/acp-16-4867-2016, 2016
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The nitrate radical (NO3) is an important nocturnal oxidant. By measuring NO3, its precursors (nitrogen dioxide and ozone) and several trace gases with which it reacts, we examined the chemical and meteorological factors influencing the lifetime of NO3 at a semi-rural mountain site. Unexpectedly long lifetimes, approaching 1 h, were observed on several nights and were associated with a low-lying residual layer. We discuss the role of other reactions that convert NO2 to NO3.
Stefan F. Schreier, Andreas Richter, Folkard Wittrock, and John P. Burrows
Atmos. Chem. Phys., 16, 2803–2817, https://doi.org/10.5194/acp-16-2803-2016, https://doi.org/10.5194/acp-16-2803-2016, 2016
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Mixing ratios of NO2 and HCHO in the free troposphere are obtained from MAX-DOAS measurements at two mountain stations at midlatitudes and in the tropics using a modified geometrical approach. The method is applied in the UV wavelength range and, thus, allows the detection of HCHO mixing ratios, in addition to NO2. We find that mixing ratios of both species are increased in the tropical free troposphere due to biomass burning.
S. Tegtmeier, F. Ziska, I. Pisso, B. Quack, G. J. M. Velders, X. Yang, and K. Krüger
Atmos. Chem. Phys., 15, 13647–13663, https://doi.org/10.5194/acp-15-13647-2015, https://doi.org/10.5194/acp-15-13647-2015, 2015
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At present, man-made halogens and natural oceanic substances both contribute to the observed ozone depletion. Emissions of the anthropogenic halogens have been reduced, whereas emissions of the natural substances are expected to increase in future climate due to anthropogenic activities affecting oceanic processes. We assess the impact of these oceanic substances on ozone by weighting their emissions with their potential to destroy ozone for current conditions and future projections.
H. Hepach, B. Quack, S. Raimund, T. Fischer, E. L. Atlas, and A. Bracher
Biogeosciences, 12, 6369–6387, https://doi.org/10.5194/bg-12-6369-2015, https://doi.org/10.5194/bg-12-6369-2015, 2015
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This manuscript covers the first measurements of CHBr3, CH2Br2 and CH3I from the equatorial Atlantic during the Cold Tongue season, identifying this region and season as a source for these compounds. For the first time, we calculated diapycnal fluxes, and showed that the fluxes from below the mixed layer to the surface are not sufficient to balance the mixed layer budget. Hence, we conclude that mixed layer production has to take place despite a pronounced sub-mixed-layer-maximum.
S. T. Lennartz, G. Krysztofiak, C. A. Marandino, B.-M. Sinnhuber, S. Tegtmeier, F. Ziska, R. Hossaini, K. Krüger, S. A. Montzka, E. Atlas, D. E. Oram, T. Keber, H. Bönisch, and B. Quack
Atmos. Chem. Phys., 15, 11753–11772, https://doi.org/10.5194/acp-15-11753-2015, https://doi.org/10.5194/acp-15-11753-2015, 2015
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Marine-produced short-lived trace gases such as halocarbons and DMS significantly impact atmospheric chemistry. To assess this impact on ozone depletion and the radiative budget, it is critical that their marine emissions in atmospheric chemistry models are quantified as accurately as possible. We show that calculating emissions online with an interactive atmosphere improves the agreement with current observations and should be employed regularly in models where marine sources are important.
J. Lampel, D. Pöhler, J. Tschritter, U. Frieß, and U. Platt
Atmos. Meas. Tech., 8, 4329–4346, https://doi.org/10.5194/amt-8-4329-2015, https://doi.org/10.5194/amt-8-4329-2015, 2015
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In recent updates of the HITRAN water vapour H2O spectroscopic compilation covering the blue spectral region (here 394–-480 nm) significant changes for the absorption bands at 416 and 426 nm were reported. In order to investigate the consistency of the different cross sections calculated from these compilations, H2O vapour column density ratios for different spectral intervals were retrieved from long-path and multi-axis differential optical absorption spectroscopy measurements.
K. D. Custard, C. R. Thompson, K. A. Pratt, P B. Shepson, J. Liao, L. G. Huey, J. J. Orlando, A. J. Weinheimer, E. Apel, S. R. Hall, F. Flocke, L. Mauldin, R. S. Hornbrook, D. Pöhler, S. General, J. Zielcke, W. R. Simpson, U. Platt, A. Fried, P. Weibring, B. C. Sive, K. Ullmann, C. Cantrell, D. J. Knapp, and D. D. Montzka
Atmos. Chem. Phys., 15, 10799–10809, https://doi.org/10.5194/acp-15-10799-2015, https://doi.org/10.5194/acp-15-10799-2015, 2015
J. Lampel, U. Frieß, and U. Platt
Atmos. Meas. Tech., 8, 3767–3787, https://doi.org/10.5194/amt-8-3767-2015, https://doi.org/10.5194/amt-8-3767-2015, 2015
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In remote sensing applications, such as differential optical absorption spectroscopy (DOAS), atmospheric scattering processes need to be considered. Inelastic scattering on air molecules can lead to filling-in of absorption lines. The contribution of rotational Raman scattering is typically corrected for. The magnitude of vibrational Raman scattering (VRS) is known from theory and agrees with our first DOAS observations of this effect. Its impact on trace-gas measurements of NO2 is discussed.
L. Kattner, B. Mathieu-Üffing, J. P. Burrows, A. Richter, S. Schmolke, A. Seyler, and F. Wittrock
Atmos. Chem. Phys., 15, 10087–10092, https://doi.org/10.5194/acp-15-10087-2015, https://doi.org/10.5194/acp-15-10087-2015, 2015
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On 1 January 2015, the International Maritime Organisation tightened the regulations for sulfur content of shipping fuels in Sulfur Emission Control Areas. Here we present data from a station near Hamburg harbour in the North Sea SECA, which uses in situ measurements of atmospheric trace gases to deduce the sulphur fuel content of passing ships. We compare data from 2014 before the regulation change and from January 2015 and show how this method can be used for compliance monitoring.
J. Gliß, N. Bobrowski, L. Vogel, D. Pöhler, and U. Platt
Atmos. Chem. Phys., 15, 5659–5681, https://doi.org/10.5194/acp-15-5659-2015, https://doi.org/10.5194/acp-15-5659-2015, 2015
I. Stemmler, I. Hense, and B. Quack
Biogeosciences, 12, 1967–1981, https://doi.org/10.5194/bg-12-1967-2015, https://doi.org/10.5194/bg-12-1967-2015, 2015
L. Surl, D. Donohoue, A. Aiuppa, N. Bobrowski, and R. von Glasow
Atmos. Chem. Phys., 15, 2613–2628, https://doi.org/10.5194/acp-15-2613-2015, https://doi.org/10.5194/acp-15-2613-2015, 2015
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We investigate the atmospheric chemistry that occurs in the plume of Mt. Etna shortly after emission.
We measured O3 destruction in the plume. Using simultaneous measurements of SO2 and wind speed, we approximate the rate of this destruction. BrO, expected to be an indicator of ozone-destructive chemistry, is also detected.
A computer model is able to approximately reproduce these results and is used to make inferences about the chemistry occurring that cannot be directly observed.
P. K. Peterson, W. R. Simpson, K. A. Pratt, P. B. Shepson, U. Frieß, J. Zielcke, U. Platt, S. J. Walsh, and S. V. Nghiem
Atmos. Chem. Phys., 15, 2119–2137, https://doi.org/10.5194/acp-15-2119-2015, https://doi.org/10.5194/acp-15-2119-2015, 2015
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We developed methods to measure the vertical distribution of bromine monoxide, a gas that oxidizes pollutants, above sea ice based upon MAX-DOAS observations from Barrow, Alaska, and find that atmospheric stability exerts a strong control on BrO's vertical distribution. Specifically, more stable (temperature inversion) situations result in BrO being closer to the ground while more neutral (not inverted) atmospheres allow BrO to ascend further aloft and grow to larger column abundance.
C. Prados-Roman, C. A. Cuevas, T. Hay, R. P. Fernandez, A. S. Mahajan, S.-J. Royer, M. Galí, R. Simó, J. Dachs, K. Großmann, D. E. Kinnison, J.-F. Lamarque, and A. Saiz-Lopez
Atmos. Chem. Phys., 15, 583–593, https://doi.org/10.5194/acp-15-583-2015, https://doi.org/10.5194/acp-15-583-2015, 2015
E. Peters, F. Wittrock, A. Richter, L. M. A. Alvarado, V. V. Rozanov, and J. P. Burrows
Atmos. Meas. Tech., 7, 4203–4221, https://doi.org/10.5194/amt-7-4203-2014, https://doi.org/10.5194/amt-7-4203-2014, 2014
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In this study, a correction spectrum accounting for insufficiencies in commonly used liquid water absorption spectra in DOAS applications is retrieved from ship-borne field measurements. The correction spectrum compensates at the same time for broadband parts of vibrational Raman scattering. With this, an entire compensation of liquid water spectral effects in DOAS applications was achieved.
L. M. A. Alvarado, A. Richter, M. Vrekoussis, F. Wittrock, A. Hilboll, S. F. Schreier, and J. P. Burrows
Atmos. Meas. Tech., 7, 4133–4150, https://doi.org/10.5194/amt-7-4133-2014, https://doi.org/10.5194/amt-7-4133-2014, 2014
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An improved glyoxal retrieval for OMI measurements using the DOAS method has been developed. The retrieval is based on sensitivity tests for the selection of most appropriate retrieval parameters. Also, corrections for reduction of interferences with other species have been applied. In addition, the link between pyrogenic emissions and glyoxal over regions with large wildfires have been investigated, and showed that fires are an important source of glyoxal.
J. Kuhn, N. Bobrowski, P. Lübcke, L. Vogel, and U. Platt
Atmos. Meas. Tech., 7, 3705–3715, https://doi.org/10.5194/amt-7-3705-2014, https://doi.org/10.5194/amt-7-3705-2014, 2014
S. General, D. Pöhler, H. Sihler, N. Bobrowski, U. Frieß, J. Zielcke, M. Horbanski, P. B. Shepson, B. H. Stirm, W. R. Simpson, K. Weber, C. Fischer, and U. Platt
Atmos. Meas. Tech., 7, 3459–3485, https://doi.org/10.5194/amt-7-3459-2014, https://doi.org/10.5194/amt-7-3459-2014, 2014
L. Kritten, A. Butz, M. P. Chipperfield, M. Dorf, S. Dhomse, R. Hossaini, H. Oelhaf, C. Prados-Roman, G. Wetzel, and K. Pfeilsticker
Atmos. Chem. Phys., 14, 9555–9566, https://doi.org/10.5194/acp-14-9555-2014, https://doi.org/10.5194/acp-14-9555-2014, 2014
I. Stemmler, I. Hense, B. Quack, and E. Maier-Reimer
Biogeosciences, 11, 4459–4476, https://doi.org/10.5194/bg-11-4459-2014, https://doi.org/10.5194/bg-11-4459-2014, 2014
P. L. Joyce, R. von Glasow, and W. R. Simpson
Atmos. Chem. Phys., 14, 7601–7616, https://doi.org/10.5194/acp-14-7601-2014, https://doi.org/10.5194/acp-14-7601-2014, 2014
K.-P. Heue, H. Riede, D. Walter, C. A. M. Brenninkmeijer, T. Wagner, U. Frieß, U. Platt, A. Zahn, G. Stratmann, and H. Ziereis
Atmos. Chem. Phys., 14, 6621–6642, https://doi.org/10.5194/acp-14-6621-2014, https://doi.org/10.5194/acp-14-6621-2014, 2014
Q. Liang, E. Atlas, D. Blake, M. Dorf, K. Pfeilsticker, and S. Schauffler
Atmos. Chem. Phys., 14, 5781–5792, https://doi.org/10.5194/acp-14-5781-2014, https://doi.org/10.5194/acp-14-5781-2014, 2014
P. Lübcke, N. Bobrowski, S. Arellano, B. Galle, G. Garzón, L. Vogel, and U. Platt
Solid Earth, 5, 409–424, https://doi.org/10.5194/se-5-409-2014, https://doi.org/10.5194/se-5-409-2014, 2014
T. Wagner, A. Apituley, S. Beirle, S. Dörner, U. Friess, J. Remmers, and R. Shaiganfar
Atmos. Meas. Tech., 7, 1289–1320, https://doi.org/10.5194/amt-7-1289-2014, https://doi.org/10.5194/amt-7-1289-2014, 2014
M. Rex, I. Wohltmann, T. Ridder, R. Lehmann, K. Rosenlof, P. Wennberg, D. Weisenstein, J. Notholt, K. Krüger, V. Mohr, and S. Tegtmeier
Atmos. Chem. Phys., 14, 4827–4841, https://doi.org/10.5194/acp-14-4827-2014, https://doi.org/10.5194/acp-14-4827-2014, 2014
S. Bleicher, J. C. Buxmann, R. Sander, T. P. Riedel, J. A. Thornton, U. Platt, and C. Zetzsch
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acpd-14-10135-2014, https://doi.org/10.5194/acpd-14-10135-2014, 2014
Revised manuscript has not been submitted
L. Cao, H. Sihler, U. Platt, and E. Gutheil
Atmos. Chem. Phys., 14, 3771–3787, https://doi.org/10.5194/acp-14-3771-2014, https://doi.org/10.5194/acp-14-3771-2014, 2014
R. Hommel, K.-U. Eichmann, J. Aschmann, K. Bramstedt, M. Weber, C. von Savigny, A. Richter, A. Rozanov, F. Wittrock, F. Khosrawi, R. Bauer, and J. P. Burrows
Atmos. Chem. Phys., 14, 3247–3276, https://doi.org/10.5194/acp-14-3247-2014, https://doi.org/10.5194/acp-14-3247-2014, 2014
C. Liu, S. Beirle, T. Butler, P. Hoor, C. Frankenberg, P. Jöckel, M. Penning de Vries, U. Platt, A. Pozzer, M. G. Lawrence, J. Lelieveld, H. Tost, and T. Wagner
Atmos. Chem. Phys., 14, 1717–1732, https://doi.org/10.5194/acp-14-1717-2014, https://doi.org/10.5194/acp-14-1717-2014, 2014
H. Hepach, B. Quack, F. Ziska, S. Fuhlbrügge, E. L. Atlas, K. Krüger, I. Peeken, and D. W. R. Wallace
Atmos. Chem. Phys., 14, 1255–1275, https://doi.org/10.5194/acp-14-1255-2014, https://doi.org/10.5194/acp-14-1255-2014, 2014
D. J. Hoch, J. Buxmann, H. Sihler, D. Pöhler, C. Zetzsch, and U. Platt
Atmos. Meas. Tech., 7, 199–214, https://doi.org/10.5194/amt-7-199-2014, https://doi.org/10.5194/amt-7-199-2014, 2014
S. Tegtmeier, K. Krüger, B. Quack, E. Atlas, D. R. Blake, H. Boenisch, A. Engel, H. Hepach, R. Hossaini, M. A. Navarro, S. Raimund, S. Sala, Q. Shi, and F. Ziska
Atmos. Chem. Phys., 13, 11869–11886, https://doi.org/10.5194/acp-13-11869-2013, https://doi.org/10.5194/acp-13-11869-2013, 2013
R. Hossaini, H. Mantle, M. P. Chipperfield, S. A. Montzka, P. Hamer, F. Ziska, B. Quack, K. Krüger, S. Tegtmeier, E. Atlas, S. Sala, A. Engel, H. Bönisch, T. Keber, D. Oram, G. Mills, C. Ordóñez, A. Saiz-Lopez, N. Warwick, Q. Liang, W. Feng, F. Moore, B. R. Miller, V. Marécal, N. A. D. Richards, M. Dorf, and K. Pfeilsticker
Atmos. Chem. Phys., 13, 11819–11838, https://doi.org/10.5194/acp-13-11819-2013, https://doi.org/10.5194/acp-13-11819-2013, 2013
R. M. Varma, S. M. Ball, T. Brauers, H.-P. Dorn, U. Heitmann, R. L. Jones, U. Platt, D. Pöhler, A. A. Ruth, A. J. L. Shillings, J. Thieser, A. Wahner, and D. S. Venables
Atmos. Meas. Tech., 6, 3115–3130, https://doi.org/10.5194/amt-6-3115-2013, https://doi.org/10.5194/amt-6-3115-2013, 2013
J. P. Parrella, K. Chance, R. J. Salawitch, T. Canty, M. Dorf, and K. Pfeilsticker
Atmos. Meas. Tech., 6, 2549–2561, https://doi.org/10.5194/amt-6-2549-2013, https://doi.org/10.5194/amt-6-2549-2013, 2013
M. von Hobe, S. Bekki, S. Borrmann, F. Cairo, F. D'Amato, G. Di Donfrancesco, A. Dörnbrack, A. Ebersoldt, M. Ebert, C. Emde, I. Engel, M. Ern, W. Frey, S. Genco, S. Griessbach, J.-U. Grooß, T. Gulde, G. Günther, E. Hösen, L. Hoffmann, V. Homonnai, C. R. Hoyle, I. S. A. Isaksen, D. R. Jackson, I. M. Jánosi, R. L. Jones, K. Kandler, C. Kalicinsky, A. Keil, S. M. Khaykin, F. Khosrawi, R. Kivi, J. Kuttippurath, J. C. Laube, F. Lefèvre, R. Lehmann, S. Ludmann, B. P. Luo, M. Marchand, J. Meyer, V. Mitev, S. Molleker, R. Müller, H. Oelhaf, F. Olschewski, Y. Orsolini, T. Peter, K. Pfeilsticker, C. Piesch, M. C. Pitts, L. R. Poole, F. D. Pope, F. Ravegnani, M. Rex, M. Riese, T. Röckmann, B. Rognerud, A. Roiger, C. Rolf, M. L. Santee, M. Scheibe, C. Schiller, H. Schlager, M. Siciliani de Cumis, N. Sitnikov, O. A. Søvde, R. Spang, N. Spelten, F. Stordal, O. Sumińska-Ebersoldt, A. Ulanovski, J. Ungermann, S. Viciani, C. M. Volk, M. vom Scheidt, P. von der Gathen, K. Walker, T. Wegner, R. Weigel, S. Weinbruch, G. Wetzel, F. G. Wienhold, I. Wohltmann, W. Woiwode, I. A. K. Young, V. Yushkov, B. Zobrist, and F. Stroh
Atmos. Chem. Phys., 13, 9233–9268, https://doi.org/10.5194/acp-13-9233-2013, https://doi.org/10.5194/acp-13-9233-2013, 2013
F. Ziska, B. Quack, K. Abrahamsson, S. D. Archer, E. Atlas, T. Bell, J. H. Butler, L. J. Carpenter, C. E. Jones, N. R. P. Harris, H. Hepach, K. G. Heumann, C. Hughes, J. Kuss, K. Krüger, P. Liss, R. M. Moore, A. Orlikowska, S. Raimund, C. E. Reeves, W. Reifenhäuser, A. D. Robinson, C. Schall, T. Tanhua, S. Tegtmeier, S. Turner, L. Wang, D. Wallace, J. Williams, H. Yamamoto, S. Yvon-Lewis, and Y. Yokouchi
Atmos. Chem. Phys., 13, 8915–8934, https://doi.org/10.5194/acp-13-8915-2013, https://doi.org/10.5194/acp-13-8915-2013, 2013
C. A. Marandino, S. Tegtmeier, K. Krüger, C. Zindler, E. L. Atlas, F. Moore, and H. W. Bange
Atmos. Chem. Phys., 13, 8427–8437, https://doi.org/10.5194/acp-13-8427-2013, https://doi.org/10.5194/acp-13-8427-2013, 2013
P. D. Hamer, V. Marécal, R. Hossaini, M. Pirre, N. Warwick, M. Chipperfield, A. A. Samah, N. Harris, A. Robinson, B. Quack, A. Engel, K. Krüger, E. Atlas, K. Subramaniam, D. Oram, E. Leedham, G. Mills, K. Pfeilsticker, S. Sala, T. Keber, H. Bönisch, L. K. Peng, M. S. M. Nadzir, P. T. Lim, A. Mujahid, A. Anton, H. Schlager, V. Catoire, G. Krysztofiak, S. Fühlbrügge, M. Dorf, and W. T. Sturges
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acpd-13-20611-2013, https://doi.org/10.5194/acpd-13-20611-2013, 2013
Revised manuscript not accepted
A. Steffen, J. Bottenheim, A. Cole, T. A. Douglas, R. Ebinghaus, U. Friess, S. Netcheva, S. Nghiem, H. Sihler, and R. Staebler
Atmos. Chem. Phys., 13, 7007–7021, https://doi.org/10.5194/acp-13-7007-2013, https://doi.org/10.5194/acp-13-7007-2013, 2013
W. Cheah, B. B. Taylor, S. Wiegmann, S. Raimund, G. Krahmann, B. Quack, and A. Bracher
Biogeosciences Discuss., https://doi.org/10.5194/bgd-10-12115-2013, https://doi.org/10.5194/bgd-10-12115-2013, 2013
Revised manuscript not accepted
S. Fuhlbrügge, K. Krüger, B. Quack, E. Atlas, H. Hepach, and F. Ziska
Atmos. Chem. Phys., 13, 6345–6357, https://doi.org/10.5194/acp-13-6345-2013, https://doi.org/10.5194/acp-13-6345-2013, 2013
S. Kreycy, C. Camy-Peyret, M. P. Chipperfield, M. Dorf, W. Feng, R. Hossaini, L. Kritten, B. Werner, and K. Pfeilsticker
Atmos. Chem. Phys., 13, 6263–6274, https://doi.org/10.5194/acp-13-6263-2013, https://doi.org/10.5194/acp-13-6263-2013, 2013
C. Hörmann, H. Sihler, N. Bobrowski, S. Beirle, M. Penning de Vries, U. Platt, and T. Wagner
Atmos. Chem. Phys., 13, 4749–4781, https://doi.org/10.5194/acp-13-4749-2013, https://doi.org/10.5194/acp-13-4749-2013, 2013
H.-P. Dorn, R. L. Apodaca, S. M. Ball, T. Brauers, S. S. Brown, J. N. Crowley, W. P. Dubé, H. Fuchs, R. Häseler, U. Heitmann, R. L. Jones, A. Kiendler-Scharr, I. Labazan, J. M. Langridge, J. Meinen, T. F. Mentel, U. Platt, D. Pöhler, F. Rohrer, A. A. Ruth, E. Schlosser, G. Schuster, A. J. L. Shillings, W. R. Simpson, J. Thieser, R. Tillmann, R. Varma, D. S. Venables, and A. Wahner
Atmos. Meas. Tech., 6, 1111–1140, https://doi.org/10.5194/amt-6-1111-2013, https://doi.org/10.5194/amt-6-1111-2013, 2013
R. A. Stachnik, L. Millán, R. Jarnot, R. Monroe, C. McLinden, S. Kühl, J. Puķīte, M. Shiotani, M. Suzuki, Y. Kasai, F. Goutail, J. P. Pommereau, M. Dorf, and K. Pfeilsticker
Atmos. Chem. Phys., 13, 3307–3319, https://doi.org/10.5194/acp-13-3307-2013, https://doi.org/10.5194/acp-13-3307-2013, 2013
P. Lübcke, N. Bobrowski, S. Illing, C. Kern, J. M. Alvarez Nieves, L. Vogel, J. Zielcke, H. Delgado Granados, and U. Platt
Atmos. Meas. Tech., 6, 677–696, https://doi.org/10.5194/amt-6-677-2013, https://doi.org/10.5194/amt-6-677-2013, 2013
G. Pinardi, M. Van Roozendael, N. Abuhassan, C. Adams, A. Cede, K. Clémer, C. Fayt, U. Frieß, M. Gil, J. Herman, C. Hermans, F. Hendrick, H. Irie, A. Merlaud, M. Navarro Comas, E. Peters, A. J. M. Piters, O. Puentedura, A. Richter, A. Schönhardt, R. Shaiganfar, E. Spinei, K. Strong, H. Takashima, M. Vrekoussis, T. Wagner, F. Wittrock, and S. Yilmaz
Atmos. Meas. Tech., 6, 167–185, https://doi.org/10.5194/amt-6-167-2013, https://doi.org/10.5194/amt-6-167-2013, 2013
C. J. Steele, S. R. Dorling, R. von Glasow, and J. Bacon
Atmos. Chem. Phys., 13, 443–461, https://doi.org/10.5194/acp-13-443-2013, https://doi.org/10.5194/acp-13-443-2013, 2013
Related subject area
Subject: Gases | Research Activity: Field Measurements | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Measurement report: Variations in surface SO2 and NOx mixing ratios from 2004 to 2016 at a background site in the North China Plain
Fate of the nitrate radical at the summit of a semi-rural mountain site in Germany assessed with direct reactivity measurements
Spatiotemporal variations of the δ(O2 ∕ N2), CO2 and δ(APO) in the troposphere over the western North Pacific
OH and HO2 radical chemistry at a suburban site during the EXPLORE-YRD campaign in 2018
Towards reconstructing the Arctic atmospheric methane history over the 20th century: measurement and modelling results for the North Greenland Ice Core Project firn
Atmospheric gas-phase composition over the Indian Ocean
Joint occurrence of heatwaves and ozone pollution and increased health risks in Beijing, China: role of synoptic weather pattern and urbanization
Using atmospheric trace gas vertical profiles to evaluate model fluxes: a case study of Arctic-CAP observations and GEOS simulations for the ABoVE domain
An evaluation of new particle formation events in Helsinki during a Baltic Sea cyanobacterial summer bloom
Oceanic emissions of dimethyl sulfide and methanethiol and their contribution to sulfur dioxide production in the marine atmosphere
An investigation into the chemistry of HONO in the marine boundary layer at Tudor Hill Marine Atmospheric Observatory in Bermuda
Tropospheric ozone production and chemical regime analysis during the COVID-19 lockdown over Europe
Overview: On the transport and transformation of pollutants in the outflow of major population centres – observational data from the EMeRGe European intensive operational period in summer 2017
Interannual variability of terpenoid emissions in an alpine city
Observations and modelling of glyoxal in the tropical Atlantic marine boundary layer
Top-down and bottom-up estimates of anthropogenic methyl bromide emissions from eastern China
Direct measurements of ozone response to emissions perturbations in California
Ground-based investigation of HOx and ozone chemistry in biomass burning plumes in rural Idaho
Insights into the significant increase in ozone during COVID-19 in a typical urban city of China
Quantification and assessment of methane emissions from offshore oil and gas facilities on the Norwegian continental shelf
Full latitudinal marine atmospheric measurements of iodine monoxide
Direct observations indicate photodegradable oxygenated volatile organic compounds (OVOCs) as larger contributors to radicals and ozone production in the atmosphere
Assessing vehicle fuel efficiency using a dense network of CO2 observations
Odds and ends of atmospheric mercury in Europe and over the North Atlantic Ocean: temporal trends of 25 years of measurements
Interpretation of NO3–N2O5 observation via steady state in high-aerosol air mass: the impact of equilibrium coefficient in ambient conditions
Global emissions of perfluorocyclobutane (PFC-318, c-C4F8) resulting from the use of hydrochlorofluorocarbon-22 (HCFC-22) feedstock to produce polytetrafluoroethylene (PTFE) and related fluorochemicals
Atmospheric measurements at Mt. Tai – Part I: HONO formation and its role in the oxidizing capacity of the upper boundary layer
Long-term trend of ozone pollution in China during 2014–2020: distinct seasonal and spatial characteristics
Urban inland wintertime N2O5 and ClNO2 influenced by snow-covered ground, air turbulence, and precipitation
First observation of mercury species on an important water vapor channel in the southeastern Tibetan Plateau
Swiss halocarbon emissions for 2019 to 2020 assessed from regional atmospheric observations
Measurement report: Long-term measurements of aerosol precursor concentrations in the Finnish subarctic boreal forest
The Fires, Asian, and Stratospheric Transport–Las Vegas Ozone Study (FAST-LVOS)
Measurement report: Long-term variations in surface NOx and SO2 mixing ratios from 2006 to 2016 at a background site in the Yangtze River Delta region, China
Atmospheric measurements at Mt. Tai – Part II: HONO budget and radical (ROx + NO3) chemistry in the lower boundary layer
Investigation of New Particle Formation mechanisms and aerosol processes at the Marambio Station, Antarctic Peninsula
Exploration of the atmospheric chemistry of nitrous acid in a coastal city of southeastern China: results from measurements across four seasons
Eddy Covariance Measurements Highlight Sources of Nitrogen Oxide Emissions Missing from Inventories for Central London
Measurement report: Ambient volatile organic compounds (VOCs) pollution at urban Beijing: characteristics, sources, and implications for pollution control
Formaldehyde evolution in US wildfire plumes during the Fire Influence on Regional to Global Environments and Air Quality experiment (FIREX-AQ)
Measurement report: Photochemical production and loss rates of formaldehyde and ozone across Europe
Is the ocean surface a source of nitrous acid (HONO) in the marine boundary layer?
Measurement report: High contributions of halocarbon and aromatic compounds to atmospheric volatile organic compounds in an industrial area
Measurement report: Fast photochemical production of peroxyacetyl nitrate (PAN) over the rural North China Plain during haze events in autumn
Long-term atmospheric emissions for the Coal Oil Point natural marine hydrocarbon seep field, offshore California
Measurement report: Observation-based formaldehyde production rates and their relation to OH reactivity around the Arabian Peninsula
Comment on “Isotopic evidence for dominant secondary production of HONO in near-ground wildfire plumes” by Chai et al. (2021)
Measurement report: Regional characteristics of seasonal and long-term variations in greenhouse gases at Nainital, India, and Comilla, Bangladesh
Nighttime and daytime dark oxidation chemistry in wildfire plumes: an observation and model analysis of FIREX-AQ aircraft data
The effects of the COVID-19 lockdowns on the composition of the troposphere as seen by In-service Aircraft for a Global Observing System (IAGOS) at Frankfurt
Xueli Liu, Liang Ran, Weili Lin, Xiaobin Xu, Zhiqiang Ma, Fan Dong, Di He, Liyan Zhou, Qingfeng Shi, and Yao Wang
Atmos. Chem. Phys., 22, 7071–7085, https://doi.org/10.5194/acp-22-7071-2022, https://doi.org/10.5194/acp-22-7071-2022, 2022
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Significant decreases in annual mean NOx from 2011 to 2016 and SO2 from 2008 to 2016 confirm the effectiveness of relevant control measures on the reduction in NOx and SO2 emissions in the North China Plain (NCP). NOx at SDZ had a weaker influence than SO2 on the emission reduction in Beijing and other areas in the NCP. An increase in the number of motor vehicles and weak traffic restrictions have caused vehicle emissions of NOx, which indicates that NOx emission control should be strengthened.
Patrick Dewald, Clara M. Nussbaumer, Jan Schuladen, Akima Ringsdorf, Achim Edtbauer, Horst Fischer, Jonathan Williams, Jos Lelieveld, and John N. Crowley
Atmos. Chem. Phys., 22, 7051–7069, https://doi.org/10.5194/acp-22-7051-2022, https://doi.org/10.5194/acp-22-7051-2022, 2022
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We measured the gas-phase reactivity of the NO3 radical on the summit (825 m a.s.l.) of a semi-rural mountain in southwestern Germany in July 2021. The impact of VOC-induced NO3 losses (mostly monoterpenes) competing with a loss by reaction with NO and photolysis throughout the diel cycle was estimated. Besides chemistry, boundary layer dynamics and plant-physiological processes presumably have a great impact on our observations, which were compared to previous NO3 measurements at the same site.
Shigeyuki Ishidoya, Kazuhiro Tsuboi, Yosuke Niwa, Hidekazu Matsueda, Shohei Murayama, Kentaro Ishijima, and Kazuyuki Saito
Atmos. Chem. Phys., 22, 6953–6970, https://doi.org/10.5194/acp-22-6953-2022, https://doi.org/10.5194/acp-22-6953-2022, 2022
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The atmospheric O2 / N2 ratio and CO2 concentration over the western North Pacific are presented. We found significant modification of the seasonal APO cycle in the middle troposphere due to the interhemispheric mixing of air. APO driven by the net marine biological activities indicated annual sea–air O2 flux during El Niño. Terrestrial biospheric and oceanic CO2 uptakes during 2012–2019 were estimated to be 1.8 and 2.8 Pg C a−1, respectively.
Xuefei Ma, Zhaofeng Tan, Keding Lu, Xinping Yang, Xiaorui Chen, Haichao Wang, Shiyi Chen, Xin Fang, Shule Li, Xin Li, Jingwei Liu, Ying Liu, Shengrong Lou, Wanyi Qiu, Hongli Wang, Limin Zeng, and Yuanhang Zhang
Atmos. Chem. Phys., 22, 7005–7028, https://doi.org/10.5194/acp-22-7005-2022, https://doi.org/10.5194/acp-22-7005-2022, 2022
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This paper presents the first OH and HO2 radical observations made in the Yangtze River Delta in China, and strong oxidation capacity is discovered based on direct measurements. The impacts of new OH regeneration mechanisms, monoterpene oxidation, and HO2 uptake processes are examined and discussed. The sources and the factors to sustain such strong oxidation are the key to understanding the ozone pollution formed in this area.
Taku Umezawa, Satoshi Sugawara, Kenji Kawamura, Ikumi Oyabu, Stephen J. Andrews, Takuya Saito, Shuji Aoki, and Takakiyo Nakazawa
Atmos. Chem. Phys., 22, 6899–6917, https://doi.org/10.5194/acp-22-6899-2022, https://doi.org/10.5194/acp-22-6899-2022, 2022
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Greenhouse gas methane in the Arctic atmosphere has not been accurately reported for 1900–1980 from either direct observations or ice core reconstructions. By using trace gas data from firn (compacted snow layers above ice sheet), air samples at two Greenland sites, and a firn air transport model, this study suggests a likely range of the Arctic methane reconstruction for the 20th century. Atmospheric scenarios from two previous studies are also evaluated for consistency with the firn data sets.
Susann Tegtmeier, Christa Marandino, Yue Jia, Birgit Quack, and Anoop S. Mahajan
Atmos. Chem. Phys., 22, 6625–6676, https://doi.org/10.5194/acp-22-6625-2022, https://doi.org/10.5194/acp-22-6625-2022, 2022
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In the atmosphere over the Indian Ocean, intense anthropogenic pollution from Southeast Asia mixes with pristine oceanic air. During the winter monsoon, high pollution levels are regularly observed over the entire northern Indian Ocean, while during the summer monsoon, clean air dominates. Here, we review current progress in detecting and understanding atmospheric gas-phase composition over the Indian Ocean and its impacts on the upper atmosphere, oceanic biogeochemistry, and marine ecosystems.
Lian Zong, Yuanjian Yang, Haiyun Xia, Meng Gao, Zhaobin Sun, Zuofang Zheng, Xianxiang Li, Guicai Ning, Yubin Li, and Simone Lolli
Atmos. Chem. Phys., 22, 6523–6538, https://doi.org/10.5194/acp-22-6523-2022, https://doi.org/10.5194/acp-22-6523-2022, 2022
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Heatwaves (HWs) paired with higher ozone (O3) concentration at surface level pose a serious threat to human health. Taking Beijing as an example, three unfavorable synoptic weather patterns were identified to dominate the compound HW and O3 pollution events. Under the synergistic stress of HWs and O3 pollution, public mortality risk increased, and synoptic patterns and urbanization enhanced the compound risk of events in Beijing by 33.09 % and 18.95 %, respectively.
Colm Sweeney, Abhishek Chatterjee, Sonja Wolter, Kathryn McKain, Robert Bogue, Stephen Conley, Tim Newberger, Lei Hu, Lesley Ott, Benjamin Poulter, Luke Schiferl, Brad Weir, Zhen Zhang, and Charles E. Miller
Atmos. Chem. Phys., 22, 6347–6364, https://doi.org/10.5194/acp-22-6347-2022, https://doi.org/10.5194/acp-22-6347-2022, 2022
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The Arctic Carbon Atmospheric Profiles (Arctic-CAP) project demonstrates the utility of aircraft profiles for independent evaluation of model-derived emissions and uptake of atmospheric CO2, CH4, and CO from land and ocean. Comparison with the Goddard Earth Observing System (GEOS) modeling system suggests that fluxes of CO2 are very consistent with observations, while those of CH4 have some regional and seasonal biases, and that CO comparison is complicated by transport errors.
Roseline C. Thakur, Lubna Dada, Lisa J. Beck, Lauriane L. J. Quéléver, Tommy Chan, Marjan Marbouti, Xu-Cheng He, Carlton Xavier, Juha Sulo, Janne Lampilahti, Markus Lampimäki, Yee Jun Tham, Nina Sarnela, Katrianne Lehtipalo, Alf Norkko, Markku Kulmala, Mikko Sipilä, and Tuija Jokinen
Atmos. Chem. Phys., 22, 6365–6391, https://doi.org/10.5194/acp-22-6365-2022, https://doi.org/10.5194/acp-22-6365-2022, 2022
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Every year intense cyanobacterial and macroalgal blooms occur in the Baltic Sea and in the coastal areas surrounding Helsinki, yet no studies have addressed the impact of biogenic emissions from these blooms on gas vapor concentrations, which in turn could influence new particle formation. This is the first study of its kind to address the chemistry driving new particle formation (NPF) during a bloom period in this region, highlighting the role of biogenic sulfuric acid and iodic acid.
Gordon A. Novak, Delaney B. Kilgour, Christopher M. Jernigan, Michael P. Vermeuel, and Timothy H. Bertram
Atmos. Chem. Phys., 22, 6309–6325, https://doi.org/10.5194/acp-22-6309-2022, https://doi.org/10.5194/acp-22-6309-2022, 2022
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We describe field measurements of the mixing ratio and oceanic emission flux of dimethyl sulfide (DMS) and methanethiol (MeSH) from a coastal ocean site. DMS is known to impact aerosol formation and growth in the marine atmosphere, influencing cloud formation and climate. Measurements of MeSH, which is produced by the same oceanic source as DMS, are rare. We show that MeSH emissions are large and must be measured alongside DMS to understand marine sulfur chemistry and aerosol formation.
Yuting Zhu, Youfeng Wang, Xianliang Zhou, Yasin F. Elshorbany, Chunxiang Ye, Matthew Hayden, and Andrew J. Peters
Atmos. Chem. Phys., 22, 6327–6346, https://doi.org/10.5194/acp-22-6327-2022, https://doi.org/10.5194/acp-22-6327-2022, 2022
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The daytime chemistry of nitrous acid (HONO), which plays an important role in the oxidation capacity of the troposphere, is not well understood. In this work, we report new field measurement results of HONO and the relevant parameters in the marine boundary layer at Tudor Hill Marine Atmospheric Observatory in Bermuda. We evaluate the daytime HONO budgets in air masses under different types of interaction with the island and examine the strengths of different HONO formation and loss mechanisms.
Clara M. Nussbaumer, Andrea Pozzer, Ivan Tadic, Lenard Röder, Florian Obersteiner, Hartwig Harder, Jos Lelieveld, and Horst Fischer
Atmos. Chem. Phys., 22, 6151–6165, https://doi.org/10.5194/acp-22-6151-2022, https://doi.org/10.5194/acp-22-6151-2022, 2022
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The European COVID-19 lockdowns have significantly reduced the emission of primary pollutants such as NOx, which impacts the tropospheric photochemical processes and the abundance of O3. In this study, we present how the lockdowns have affected tropospheric trace gases and ozone production based on in situ observations and modeling simulations. We additionally show that the chemical regime shifted from a transition point to a NOx limitation in the upper troposphere.
M. Dolores Andrés Hernández, Andreas Hilboll, Helmut Ziereis, Eric Förster, Ovid O. Krüger, Katharina Kaiser, Johannes Schneider, Francesca Barnaba, Mihalis Vrekoussis, Jörg Schmidt, Heidi Huntrieser, Anne-Marlene Blechschmidt, Midhun George, Vladyslav Nenakhov, Theresa Harlass, Bruna A. Holanda, Jennifer Wolf, Lisa Eirenschmalz, Marc Krebsbach, Mira L. Pöhlker, Anna B. Kalisz Hedegaard, Linlu Mei, Klaus Pfeilsticker, Yangzhuoran Liu, Ralf Koppmann, Hans Schlager, Birger Bohn, Ulrich Schumann, Andreas Richter, Benjamin Schreiner, Daniel Sauer, Robert Baumann, Mariano Mertens, Patrick Jöckel, Markus Kilian, Greta Stratmann, Christopher Pöhlker, Monica Campanelli, Marco Pandolfi, Michael Sicard, José L. Gómez-Amo, Manuel Pujadas, Katja Bigge, Flora Kluge, Anja Schwarz, Nikos Daskalakis, David Walter, Andreas Zahn, Ulrich Pöschl, Harald Bönisch, Stephan Borrmann, Ulrich Platt, and John P. Burrows
Atmos. Chem. Phys., 22, 5877–5924, https://doi.org/10.5194/acp-22-5877-2022, https://doi.org/10.5194/acp-22-5877-2022, 2022
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EMeRGe provides a unique set of in situ and remote sensing airborne measurements of trace gases and aerosol particles along selected flight routes in the lower troposphere over Europe. The interpretation uses also complementary collocated ground-based and satellite measurements. The collected data help to improve the current understanding of the complex spatial distribution of trace gases and aerosol particles resulting from mixing, transport, and transformation of pollution plumes over Europe.
Lisa Kaser, Arianna Peron, Martin Graus, Marcus Striednig, Georg Wohlfahrt, Stanislav Juráň, and Thomas Karl
Atmos. Chem. Phys., 22, 5603–5618, https://doi.org/10.5194/acp-22-5603-2022, https://doi.org/10.5194/acp-22-5603-2022, 2022
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Biogenic volatile organic compounds (e.g., terpenoids) play an essential role in atmospheric chemistry. Urban greening activities need to consider the ozone- and aerosol-forming potential of these compounds released from vegetation. NMVOC emissions in urban environments are complex, and the biogenic component remains poorly quantified. For summer conditions biogenic emissions dominate terpene emissions and heat waves can significantly modulate urban biogenic terpenoid emissions.
Hannah Walker, Daniel Stone, Trevor Ingham, Sina Hackenberg, Danny Cryer, Shalini Punjabi, Katie Read, James Lee, Lisa Whalley, Dominick V. Spracklen, Lucy J. Carpenter, Steve R. Arnold, and Dwayne E. Heard
Atmos. Chem. Phys., 22, 5535–5557, https://doi.org/10.5194/acp-22-5535-2022, https://doi.org/10.5194/acp-22-5535-2022, 2022
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Glyoxal is a ubiquitous reactive organic compound in the atmosphere, which may form organic aerosol and impact the atmosphere's oxidising capacity. There are limited measurements of glyoxal's abundance in the remote marine atmosphere. We made new measurements of glyoxal using a highly sensitive technique over two 4-week periods in the tropical Atlantic atmosphere. We show that daytime measurements are mostly consistent with our chemical understanding but a potential missing source at night.
Haklim Choi, Mi-Kyung Park, Paul J. Fraser, Hyeri Park, Sohyeon Geum, Jens Mühle, Jooil Kim, Ian Porter, Peter K. Salameh, Christina M. Harth, Bronwyn L. Dunse, Paul B. Krummel, Ray F. Weiss, Simon O'Doherty, Dickon Young, and Sunyoung Park
Atmos. Chem. Phys., 22, 5157–5173, https://doi.org/10.5194/acp-22-5157-2022, https://doi.org/10.5194/acp-22-5157-2022, 2022
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We observed 12-year continuous CH3Br pollution signals at Gosan and estimated anthropogenic CH3Br emissions in eastern China. The analysis revealed a significant discrepancy between top-down estimates and the bottom-up emissions from the fumigation usage reported to the United Nations Environment Programme, likely due to unreported or inaccurately reported fumigation usage. This result provides information to monitor international compliance with the Montreal Protocol.
Shenglun Wu, Hyung Joo Lee, Andrea Anderson, Shang Liu, Toshihiro Kuwayama, John H. Seinfeld, and Michael J. Kleeman
Atmos. Chem. Phys., 22, 4929–4949, https://doi.org/10.5194/acp-22-4929-2022, https://doi.org/10.5194/acp-22-4929-2022, 2022
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An ozone control experiment usually conducted in the laboratory was installed in a trailer and moved to the outdoor environment to directly confirm that we are controlling the right sources in order to lower ambient ozone concentrations. Adding small amounts of precursor oxides of nitrogen and volatile organic compounds to ambient air showed that the highest ozone concentrations are best controlled by reducing concentrations of oxides of nitrogen. The results confirm satellite measurements.
Andrew J. Lindsay, Daniel C. Anderson, Rebecca A. Wernis, Yutong Liang, Allen H. Goldstein, Scott C. Herndon, Joseph R. Roscioli, Christoph Dyroff, Ed C. Fortner, Philip L. Croteau, Francesca Majluf, Jordan E. Krechmer, Tara I. Yacovitch, Walter B. Knighton, and Ezra C. Wood
Atmos. Chem. Phys., 22, 4909–4928, https://doi.org/10.5194/acp-22-4909-2022, https://doi.org/10.5194/acp-22-4909-2022, 2022
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Wildfire smoke dramatically impacts air quality and often has elevated concentrations of ozone. We present measurements of ozone and its precursors at a rural site periodically impacted by wildfire smoke. Measurements of total peroxy radicals, key ozone precursors that have been studied little within wildfires, compare well with chemical box model predictions. Our results indicate no serious issues with using current chemistry mechanisms to model chemistry in aged wildfire plumes.
Kun Zhang, Zhiqiang Liu, Xiaojuan Zhang, Qing Li, Andrew Jensen, Wen Tan, Ling Huang, Yangjun Wang, Joost de Gouw, and Li Li
Atmos. Chem. Phys., 22, 4853–4866, https://doi.org/10.5194/acp-22-4853-2022, https://doi.org/10.5194/acp-22-4853-2022, 2022
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A significant increase in O3 concentrations was found during the lockdown period of COVID-19 in most areas of China. By field measurements coupled with machine learning, an observation-based model (OBM) and sensitivity analysis, we found the changes in the NOx / VOC ratio were a key reason for the significant rise in O3. To restrain O3 pollution, more efforts should be devoted to the control of anthropogenic OVOCs, alkenes and aromatics.
Amy Foulds, Grant Allen, Jacob T. Shaw, Prudence Bateson, Patrick A. Barker, Langwen Huang, Joseph R. Pitt, James D. Lee, Shona E. Wilde, Pamela Dominutti, Ruth M. Purvis, David Lowry, James L. France, Rebecca E. Fisher, Alina Fiehn, Magdalena Pühl, Stéphane J. B. Bauguitte, Stephen A. Conley, Mackenzie L. Smith, Tom Lachlan-Cope, Ignacio Pisso, and Stefan Schwietzke
Atmos. Chem. Phys., 22, 4303–4322, https://doi.org/10.5194/acp-22-4303-2022, https://doi.org/10.5194/acp-22-4303-2022, 2022
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We measured CH4 emissions from 21 offshore oil and gas facilities in the Norwegian Sea in 2019. Measurements compared well with operator-reported emissions but were greatly underestimated when compared with a 2016 global fossil fuel inventory. This study demonstrates the need for up-to-date and accurate inventories for use in research and policy and the important benefits of best-practice reporting methods by operators. Airborne measurements are an effective tool to validate such inventories.
Hisahiro Takashima, Yugo Kanaya, Saki Kato, Martina M. Friedrich, Michel Van Roozendael, Fumikazu Taketani, Takuma Miyakawa, Yuichi Komazaki, Carlos A. Cuevas, Alfonso Saiz-Lopez, and Takashi Sekiya
Atmos. Chem. Phys., 22, 4005–4018, https://doi.org/10.5194/acp-22-4005-2022, https://doi.org/10.5194/acp-22-4005-2022, 2022
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We have undertaken atmospheric iodine monoxide (IO) observations in the global marine boundary layer with a wide latitudinal coverage and sea surface temperature (SST) range. We conclude that atmospheric iodine is abundant over the Western Pacific warm pool, appearing as an iodine fountain, where ozone (O3) minima occur. Our study also found negative correlations between IO and O3 concentrations over IO maxima, which requires reconsideration of the initiation process of halogen activation.
Wenjie Wang, Bin Yuan, Yuwen Peng, Hang Su, Yafang Cheng, Suxia Yang, Caihong Wu, Jipeng Qi, Fengxia Bao, Yibo Huangfu, Chaomin Wang, Chenshuo Ye, Zelong Wang, Baolin Wang, Xinming Wang, Wei Song, Weiwei Hu, Peng Cheng, Manni Zhu, Junyu Zheng, and Min Shao
Atmos. Chem. Phys., 22, 4117–4128, https://doi.org/10.5194/acp-22-4117-2022, https://doi.org/10.5194/acp-22-4117-2022, 2022
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From thorough measurements of numerous oxygenated volatile organic compounds, we show that their photodissociation can be important for radical production and ozone formation in the atmosphere. This effect was underestimated in previous studies, as measurements of them were lacking.
Helen L. Fitzmaurice, Alexander J. Turner, Jinsol Kim, Katherine Chan, Erin R. Delaria, Catherine Newman, Paul Wooldridge, and Ronald C. Cohen
Atmos. Chem. Phys., 22, 3891–3900, https://doi.org/10.5194/acp-22-3891-2022, https://doi.org/10.5194/acp-22-3891-2022, 2022
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On-road emissions are thought to vary widely from existing predictions, as the effects of the age of the vehicle fleet, the performance of emission control systems, and variations in speed are difficult to assess under ambient driving conditions. We present an observational approach to characterize on-road emissions and show that the method is consistent with other approaches to within ~ 3 %.
Danilo Custódio, Katrine Aspmo Pfaffhuber, T. Gerard Spain, Fidel F. Pankratov, Iana Strigunova, Koketso Molepo, Henrik Skov, Johannes Bieser, and Ralf Ebinghaus
Atmos. Chem. Phys., 22, 3827–3840, https://doi.org/10.5194/acp-22-3827-2022, https://doi.org/10.5194/acp-22-3827-2022, 2022
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As a poison in the air that we breathe and the food that we eat, mercury is a human health concern for society as a whole. In that regard, this work deals with monitoring and modelling mercury in the environment, improving wherewithal, identifying the strength of the different components at play, and interpreting information to support the efforts that seek to safeguard public health.
Xiaorui Chen, Haichao Wang, and Keding Lu
Atmos. Chem. Phys., 22, 3525–3533, https://doi.org/10.5194/acp-22-3525-2022, https://doi.org/10.5194/acp-22-3525-2022, 2022
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We use a complete set of simulations to evaluate whether equilibrium and steady state are appropriate for a chemical system involving several reactive nitrogen-containing species (NO2, NO3, and N2O5) under various conditions. A previously neglected bias for the coefficient applied for interpreting their effects is disclosed, and the relevant ambient factors are examined. We therefore provide a good solution to an accurate representation of nighttime chemistry in high-aerosol areas.
Jens Mühle, Lambert J. M. Kuijpers, Kieran M. Stanley, Matthew Rigby, Luke M. Western, Jooil Kim, Sunyoung Park, Christina M. Harth, Paul B. Krummel, Paul J. Fraser, Simon O'Doherty, Peter K. Salameh, Roland Schmidt, Dickon Young, Ronald G. Prinn, Ray H. J. Wang, and Ray F. Weiss
Atmos. Chem. Phys., 22, 3371–3378, https://doi.org/10.5194/acp-22-3371-2022, https://doi.org/10.5194/acp-22-3371-2022, 2022
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Emissions of the strong greenhouse gas perfluorocyclobutane (c-C4F8) into the atmosphere have been increasing sharply since the early 2000s. These c-C4F8 emissions are highly correlated with the amount of hydrochlorofluorocarbon-22 produced to synthesize polytetrafluoroethylene (known for its non-stick properties) and related chemicals. From this process, c-C4F8 by-product is vented to the atmosphere. Avoiding these unnecessary c-C4F8 emissions could reduce the climate impact of this industry.
Chaoyang Xue, Can Ye, Jörg Kleffmann, Chenglong Zhang, Valéry Catoire, Fengxia Bao, Abdelwahid Mellouki, Likun Xue, Jianmin Chen, Keding Lu, Yong Zhao, Hengde Liu, Zhaoxin Guo, and Yujing Mu
Atmos. Chem. Phys., 22, 3149–3167, https://doi.org/10.5194/acp-22-3149-2022, https://doi.org/10.5194/acp-22-3149-2022, 2022
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Summertime measurements of nitrous acid (HONO) and related parameters were conducted at the foot and the summit of Mt. Tai (1534 m above sea level). We proposed a rapid vertical air mass exchange between the foot and the summit level, which enhances the role of HONO in the oxidizing capacity of the upper boundary layer. Kinetics for aerosol-derived HONO sources were constrained. HONO formation from different paths was quantified and discussed.
Wenjie Wang, David Parrish, Siwen Wang, Fengxia Bao, Ruijing Ni, Xin Li, Suding Yang, Hongli Wang, Yafang Cheng, and Hang Su
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2022-123, https://doi.org/10.5194/acp-2022-123, 2022
Revised manuscript accepted for ACP
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Tropospheric ozone is an air pollutant that is detrimental to human health, vegetation and ecosystem productivity. A comprehensive characterization of the spatial and temporal distribution of tropospheric ozone is critical to our understanding of these issues. Here we summarize this distribution over China from the available observational records to the extent possible. This study provides insights into efficient future ozone control strategies in China.
Kathryn D. Kulju, Stephen M. McNamara, Qianjie Chen, Hannah S. Kenagy, Jacinta Edebeli, Jose D. Fuentes, Steven B. Bertman, and Kerri A. Pratt
Atmos. Chem. Phys., 22, 2553–2568, https://doi.org/10.5194/acp-22-2553-2022, https://doi.org/10.5194/acp-22-2553-2022, 2022
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N2O5 uptake by chloride-containing surfaces produces ClNO2, which photolyzes, producing NO2 and highly reactive Cl radicals that impact air quality. In the inland urban atmosphere, ClNO2 was elevated during lower air turbulence and over snow-covered ground, from snowpack ClNO2 production. N2O5 and ClNO2 levels were lowest, on average, during rainfall and fog because of scavenging, with N2O5 scavenging by fog droplets likely contributing to observed increased particulate nitrate concentrations.
Huiming Lin, Yindong Tong, Chenghao Yu, Long Chen, Xiufeng Yin, Qianggong Zhang, Shichang Kang, Lun Luo, James Schauer, Benjamin de Foy, and Xuejun Wang
Atmos. Chem. Phys., 22, 2651–2668, https://doi.org/10.5194/acp-22-2651-2022, https://doi.org/10.5194/acp-22-2651-2022, 2022
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The Tibetan Plateau is known as
The Third Poleand is generally considered to be a clean area owing to its high altitude. However, it may receive be impacted by air pollutants transported from the Indian subcontinent. Pollutants generally enter the Tibetan Plateau in several ways. Among them is the Yarlung Zangbu–Brahmaputra Grand Canyon. In this study, we identified the influence of the Indian summer monsoon on the origin, transport, and behavior of mercury in this area.
Dominique Rust, Ioannis Katharopoulos, Martin K. Vollmer, Stephan Henne, Simon O'Doherty, Daniel Say, Lukas Emmenegger, Renato Zenobi, and Stefan Reimann
Atmos. Chem. Phys., 22, 2447–2466, https://doi.org/10.5194/acp-22-2447-2022, https://doi.org/10.5194/acp-22-2447-2022, 2022
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Artificial halocarbons contribute to ozone layer depletion and to global warming. We measured the atmospheric concentrations of halocarbons at the Beromünster tower, modelled the Swiss emissions, and compared the results to the internationally reported Swiss emissions inventory. For most of the halocarbons, we found good agreement, whereas one refrigerant might be overestimated in the inventory. In addition, we present first emission estimates of the newest types of halocarbons.
Tuija Jokinen, Katrianne Lehtipalo, Roseline Cutting Thakur, Ilona Ylivinkka, Kimmo Neitola, Nina Sarnela, Totti Laitinen, Markku Kulmala, Tuukka Petäjä, and Mikko Sipilä
Atmos. Chem. Phys., 22, 2237–2254, https://doi.org/10.5194/acp-22-2237-2022, https://doi.org/10.5194/acp-22-2237-2022, 2022
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New particle formation is an important source of cloud condensation nuclei; however, long-term measurements of aerosol-forming vapors are close to nonexistent in the Arctic. Here, we report 7 months of CI-APi-TOF measurements of sulfuric acid, iodic acid, methane sulfonic acid and the sum of highly oxygenated organic molecules from the SMEAR I station in the Finnish subarctic. The results help us to understand atmospheric chemical processes and aerosol formation in this rapidly changing area.
Andrew O. Langford, Christoph J. Senff, Raul J. Alvarez II, Ken C. Aikin, Sunil Baidar, Timothy A. Bonin, W. Alan Brewer, Jerome Brioude, Steven S. Brown, Joel D. Burley, Dani J. Caputi, Stephen A. Conley, Patrick D. Cullis, Zachary C. J. Decker, Stéphanie Evan, Guillaume Kirgis, Meiyun Lin, Mariusz Pagowski, Jeff Peischl, Irina Petropavlovskikh, R. Bradley Pierce, Thomas B. Ryerson, Scott P. Sandberg, Chance W. Sterling, Ann M. Weickmann, and Li Zhang
Atmos. Chem. Phys., 22, 1707–1737, https://doi.org/10.5194/acp-22-1707-2022, https://doi.org/10.5194/acp-22-1707-2022, 2022
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The Fires, Asian, and Stratospheric Transport–Las Vegas Ozone Study (FAST-LVOS) combined lidar, aircraft, and in situ measurements with global models to investigate the contributions of stratospheric intrusions, regional and Asian pollution, and wildfires to background ozone in the southwestern US during May and June 2017 and demonstrated that these processes contributed to background ozone levels that exceeded 70 % of the US National Ambient Air Quality Standard during the 6-week campaign.
Qingqing Yin, Qianli Ma, Weili Lin, Xiaobin Xu, and Jie Yao
Atmos. Chem. Phys., 22, 1015–1033, https://doi.org/10.5194/acp-22-1015-2022, https://doi.org/10.5194/acp-22-1015-2022, 2022
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China has been experiencing rapid changes in emissions of air pollutants in recent decades. NOx and SO2 measurements from 2006 to 2016 at the Lin’an World Meteorological Organization Global Atmospheric Watch station were used to characterize the seasonal and diurnal variations and study the long-term trends. This study reaffirms China’s success in controlling both NOx and SO2 in the Yangtze River Delta but indicates at the same time a necessity to strengthen the NOx emission control.
Chaoyang Xue, Can Ye, Jörg Kleffmann, Wenjin Zhang, Xiaowei He, Pengfei Liu, Chenglong Zhang, Xiaoxi Zhao, Chengtang Liu, Zhuobiao Ma, Junfeng Liu, Jinhe Wang, Keding Lu, Valéry Catoire, Abdelwahid Mellouki, and Yujing Mu
Atmos. Chem. Phys., 22, 1035–1057, https://doi.org/10.5194/acp-22-1035-2022, https://doi.org/10.5194/acp-22-1035-2022, 2022
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Nitrous acid (HONO) and related parameters were measured at the foot and the summit of Mt. Tai in the summer of 2018. Based on measurements at the foot station, we utilized a box model to explore the roles of different sources in the HONO budget. We also studied radical chemistry in this high-ozone region.
Lauriane L. J. Quéléver, Lubna Dada, Eija Asmi, Janne Lampilahti, Tommy Chan, Jonathan E. Ferrara, Gustavo E. Copes, German Pérez-Fogwill, Luis Barreira, Minna Aurela, Douglas R. Worsnop, Tuija Jokinen, and Mikko Sipila
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2021-1063, https://doi.org/10.5194/acp-2021-1063, 2022
Revised manuscript accepted for ACP
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Understanding how aerosol form is crucial to correctly model the climate and improve future predictions. This work provides an extensive analysis of aerosol particles and their precursors at the Marambio research Station, Antarctic Peninsula. We show that Sulfuric Acid, Ammonia and Dimethyl amine are key contributors for the frequent new particle formation events observed at site. We discuss nucleation mechanisms and highlight the need of targeted measurement to fully understand these processes.
Baoye Hu, Jun Duan, Youwei Hong, Lingling Xu, Mengren Li, Yahui Bian, Min Qin, Wu Fang, Pinhua Xie, and Jinsheng Chen
Atmos. Chem. Phys., 22, 371–393, https://doi.org/10.5194/acp-22-371-2022, https://doi.org/10.5194/acp-22-371-2022, 2022
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There has been a lack of research into HONO in coastal cities with low concentrations of PM2.5, but strong sunlight and high humidity. Insufficient research on coastal cities with good air quality has resulted in certain obstacles to assessing the photochemical processes in these areas. Furthermore, HONO contributes to the atmospheric photochemistry depending on the season. Therefore, observations of HONO across four seasons in the southeastern coastal area of China are urgently needed.
Will S. Drysdale, Adam R. Vaughan, Freya A. Squires, Sam J. Cliff, Stefan Metzger, David Durden, Natchaya Pingintha-Durden, Carole Helfter, Eiko Nemitz, C. Sue B. Grimmond, Janet Barlow, Sean Beevers, Gregor Stewart, David Dajnak, Ruth M. Purvis, and James D. Lee
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2021-982, https://doi.org/10.5194/acp-2021-982, 2022
Revised manuscript accepted for ACP
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Measurements of nitrogen oxide and nitrogen dioxide (NOx) emissions are important for a good understanding of air quality. While there are many direct measurements of NOx concentration, there are very few measurements of its emission. Measurements of emissions provide constraints to emissions inventories and air quality models. This article presents measurements of NOx emission from the BT Tower in central London in 2017, and compares them with inventories, finding they underestimate by ~1.48 x.
Lulu Cui, Di Wu, Shuxiao Wang, Qingcheng Xu, Ruolan Hu, and Jiming Hao
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2021-959, https://doi.org/10.5194/acp-2021-959, 2021
Revised manuscript accepted for ACP
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A one-year campaign was conducted to characterize VOCs at an urban site in Beijing during different episodes. VOCs from fuel evaporation and diesel exhaust particularly toluene, xylenes, trans-2-butene, acrolein, methyl methacrylate, vinyl acetate, 1-butene and 1-hexene were the main contributors. VOCs from diesel exhaust and coal/biomass combustion were found to be the dominant contributors for SOAFP, particularly the VOC species of toluene, 1-hexene, xylenes, ethylbenzene and styrene.
Jin Liao, Glenn M. Wolfe, Reem A. Hannun, Jason M. St. Clair, Thomas F. Hanisco, Jessica B. Gilman, Aaron Lamplugh, Vanessa Selimovic, Glenn S. Diskin, John B. Nowak, Hannah S. Halliday, Joshua P. DiGangi, Samuel R. Hall, Kirk Ullmann, Christopher D. Holmes, Charles H. Fite, Anxhelo Agastra, Thomas B. Ryerson, Jeff Peischl, Ilann Bourgeois, Carsten Warneke, Matthew M. Coggon, Georgios I. Gkatzelis, Kanako Sekimoto, Alan Fried, Dirk Richter, Petter Weibring, Eric C. Apel, Rebecca S. Hornbrook, Steven S. Brown, Caroline C. Womack, Michael A. Robinson, Rebecca A. Washenfelder, Patrick R. Veres, and J. Andrew Neuman
Atmos. Chem. Phys., 21, 18319–18331, https://doi.org/10.5194/acp-21-18319-2021, https://doi.org/10.5194/acp-21-18319-2021, 2021
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Formaldehyde (HCHO) is an important oxidant precursor and affects the formation of O3 and other secondary pollutants in wildfire plumes. We disentangle the processes controlling HCHO evolution from wildfire plumes sampled by NASA DC-8 during FIREX-AQ. We find that OH abundance rather than normalized OH reactivity is the main driver of fire-to-fire variability in HCHO secondary production and estimate an effective HCHO yield per volatile organic compound molecule oxidized in wildfire plumes.
Clara M. Nussbaumer, John N. Crowley, Jan Schuladen, Jonathan Williams, Sascha Hafermann, Andreas Reiffs, Raoul Axinte, Hartwig Harder, Cheryl Ernest, Anna Novelli, Katrin Sala, Monica Martinez, Chinmay Mallik, Laura Tomsche, Christian Plass-Dülmer, Birger Bohn, Jos Lelieveld, and Horst Fischer
Atmos. Chem. Phys., 21, 18413–18432, https://doi.org/10.5194/acp-21-18413-2021, https://doi.org/10.5194/acp-21-18413-2021, 2021
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HCHO is an important atmospheric trace gas influencing the photochemical processes in the Earth’s atmosphere, including the budget of HOx and the abundance of tropospheric O3. This research presents the photochemical calculations of HCHO and O3 based on three field campaigns across Europe. We show that HCHO production via the oxidation of only four volatile organic compound precursors, i.e., CH4, CH3CHO, C5H8 and CH3OH, can balance the observed loss at all sites well.
Leigh R. Crilley, Louisa J. Kramer, Francis D. Pope, Chris Reed, James D. Lee, Lucy J. Carpenter, Lloyd D. J. Hollis, Stephen M. Ball, and William J. Bloss
Atmos. Chem. Phys., 21, 18213–18225, https://doi.org/10.5194/acp-21-18213-2021, https://doi.org/10.5194/acp-21-18213-2021, 2021
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Nitrous acid (HONO) is a key source of atmospheric oxidants. We evaluate if the ocean surface is a source of HONO for the marine boundary layer, using measurements from two contrasting coastal locations. We observed no evidence for a night-time ocean surface source, in contrast to previous work. This points to significant geographical variation in the predominant HONO formation mechanisms in marine environments, reflecting possible variability in the sea-surface microlayer composition.
Ahsan Mozaffar, Yan-Lin Zhang, Yu-Chi Lin, Feng Xie, Mei-Yi Fan, and Fang Cao
Atmos. Chem. Phys., 21, 18087–18099, https://doi.org/10.5194/acp-21-18087-2021, https://doi.org/10.5194/acp-21-18087-2021, 2021
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We performed a long-term investigation of ambient volatile organic compounds (VOCs) in an industrial area in Nanjing, China. Followed by alkanes, halocarbons and aromatics were the most abundant VOC groups. Vehicle-related emissions were the major VOC sources in the study area. Aromatic and alkene VOCs were responsible for most of the atmospheric reactions.
Yulu Qiu, Zhiqiang Ma, Ke Li, Mengyu Huang, Jiujiang Sheng, Ping Tian, Jia Zhu, Weiwei Pu, Yingxiao Tang, Tingting Han, Huaigang Zhou, and Hong Liao
Atmos. Chem. Phys., 21, 17995–18010, https://doi.org/10.5194/acp-21-17995-2021, https://doi.org/10.5194/acp-21-17995-2021, 2021
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Photochemical pollution over the North China Plain (NCP) is attracting much concern. Our observations at a rural site in the NCP identified high peroxyacetyl nitrate (PAN) concentrations, even on cold days. Increased acetaldehyde concentration and hydroxyl radical production rates drive fast PAN formation. Moreover, our study emphasizes the importance of formaldehyde photolysis in PAN formation and calls for implementing strict volatile organic compound controls after summer over the NCP.
Ira Leifer, Christopher Melton, and Donald R. Blake
Atmos. Chem. Phys., 21, 17607–17629, https://doi.org/10.5194/acp-21-17607-2021, https://doi.org/10.5194/acp-21-17607-2021, 2021
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We demonstrate a novel application using air quality station data to derive 3-decade-averaged emissions from the Coal Oil Point (COP) seep field, a highly spatially and temporally variable geological migration system. Emissions were 19 Gg per year, suggesting that the COP seep field contributes 0.27 % of the global marine seep budget based on a recent estimate. This provides an advance over snapshot survey values by accounting for seasonal and interannual variations.
Dirk Dienhart, John N. Crowley, Efstratios Bourtsoukidis, Achim Edtbauer, Philipp G. Eger, Lisa Ernle, Hartwig Harder, Bettina Hottmann, Monica Martinez, Uwe Parchatka, Jean-Daniel Paris, Eva Y. Pfannerstill, Roland Rohloff, Jan Schuladen, Christof Stönner, Ivan Tadic, Sebastian Tauer, Nijing Wang, Jonathan Williams, Jos Lelieveld, and Horst Fischer
Atmos. Chem. Phys., 21, 17373–17388, https://doi.org/10.5194/acp-21-17373-2021, https://doi.org/10.5194/acp-21-17373-2021, 2021
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We present the first ship-based in situ measurements of formaldehyde (HCHO), hydroxyl radicals (OH) and the OH reactivity around the Arabian Peninsula. Regression analysis of the HCHO production rate and the related OH chemistry revealed the regional HCHO yield αeff, which represents the different chemical regimes encountered. Highest values were found for the Arabian Gulf (also known as the Persian Gulf), which highlights this region as a hotspot of photochemical air pollution.
James M. Roberts
Atmos. Chem. Phys., 21, 16793–16795, https://doi.org/10.5194/acp-21-16793-2021, https://doi.org/10.5194/acp-21-16793-2021, 2021
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This comment provides evidence that recently reported measurements of the isotope composition of wildfire-derived oxides of nitrogen have a significant interference from other nitrogen compounds. In addition, the conceptual model used to interpret the results was missing several key reactions.
Shohei Nomura, Manish Naja, M. Kawser Ahmed, Hitoshi Mukai, Yukio Terao, Toshinobu Machida, Motoki Sasakawa, and Prabir K. Patra
Atmos. Chem. Phys., 21, 16427–16452, https://doi.org/10.5194/acp-21-16427-2021, https://doi.org/10.5194/acp-21-16427-2021, 2021
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Long-term measurements of greenhouse gases (GHGs) in India and Bangladesh unveiled specific characteristics in their variations in these regions. Plants including rice cultivated in winter and summer strongly affected seasonal variations and levels in CO2 and CH4. Long-term variability of GHGs showed quite different features in their growth rates from those in Mauna Loa. GHG trends in this region seemed to be hardly affected by El Niño–Southern Oscillation (ENSO).
Zachary C. J. Decker, Michael A. Robinson, Kelley C. Barsanti, Ilann Bourgeois, Matthew M. Coggon, Joshua P. DiGangi, Glenn S. Diskin, Frank M. Flocke, Alessandro Franchin, Carley D. Fredrickson, Georgios I. Gkatzelis, Samuel R. Hall, Hannah Halliday, Christopher D. Holmes, L. Gregory Huey, Young Ro Lee, Jakob Lindaas, Ann M. Middlebrook, Denise D. Montzka, Richard Moore, J. Andrew Neuman, John B. Nowak, Brett B. Palm, Jeff Peischl, Felix Piel, Pamela S. Rickly, Andrew W. Rollins, Thomas B. Ryerson, Rebecca H. Schwantes, Kanako Sekimoto, Lee Thornhill, Joel A. Thornton, Geoffrey S. Tyndall, Kirk Ullmann, Paul Van Rooy, Patrick R. Veres, Carsten Warneke, Rebecca A. Washenfelder, Andrew J. Weinheimer, Elizabeth Wiggins, Edward Winstead, Armin Wisthaler, Caroline Womack, and Steven S. Brown
Atmos. Chem. Phys., 21, 16293–16317, https://doi.org/10.5194/acp-21-16293-2021, https://doi.org/10.5194/acp-21-16293-2021, 2021
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To understand air quality impacts from wildfires, we need an accurate picture of how wildfire smoke changes chemically both day and night as sunlight changes the chemistry of smoke. We present a chemical analysis of wildfire smoke as it changes from midday through the night. We use aircraft observations from the FIREX-AQ field campaign with a chemical box model. We find that even under sunlight typical
nighttimechemistry thrives and controls the fate of key smoke plume chemical processes.
Hannah Clark, Yasmine Bennouna, Maria Tsivlidou, Pawel Wolff, Bastien Sauvage, Brice Barret, Eric Le Flochmoën, Romain Blot, Damien Boulanger, Jean-Marc Cousin, Philippe Nédélec, Andreas Petzold, and Valérie Thouret
Atmos. Chem. Phys., 21, 16237–16256, https://doi.org/10.5194/acp-21-16237-2021, https://doi.org/10.5194/acp-21-16237-2021, 2021
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We examined 27 years of IAGOS (In-service Aircraft for a Global Observing System) profiles at Frankfurt to see if there were unusual features during the spring of 2020 related to COVID-19 lockdowns in Europe. Increased ozone near the surface was partly linked to the reduction in emissions. Carbon monoxide decreased near the surface, but the impact of the lockdowns was offset by polluted air masses from elsewhere. There were small reductions in ozone and carbon monoxide in the free troposphere.
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