Articles | Volume 13, issue 16
https://doi.org/10.5194/acp-13-8427-2013
© Author(s) 2013. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Special issue:
https://doi.org/10.5194/acp-13-8427-2013
© Author(s) 2013. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Research article
| 
26 Aug 2013
Research article |
| 26 Aug 2013
Dimethylsulphide (DMS) emissions from the western Pacific Ocean: a potential marine source for stratospheric sulphur?
C. A. Marandino
GEOMAR Helmholtz-Zentrum für Ozeanforschung Kiel, Düsternbrooker Weg 20, 24105 Kiel, Germany
S. Tegtmeier
GEOMAR Helmholtz-Zentrum für Ozeanforschung Kiel, Düsternbrooker Weg 20, 24105 Kiel, Germany
K. Krüger
GEOMAR Helmholtz-Zentrum für Ozeanforschung Kiel, Düsternbrooker Weg 20, 24105 Kiel, Germany
C. Zindler
GEOMAR Helmholtz-Zentrum für Ozeanforschung Kiel, Düsternbrooker Weg 20, 24105 Kiel, Germany
E. L. Atlas
RSMAS/MAC, University of Miami, 4600 Rickenbacker Causeway, Miami, FL 33149, USA
F. Moore
NOAA/Earth System Reasearch Laboratory (NOAA/ESRL), 325 Broadway, Boulder, CO 80305-3337, USA
H. W. Bange
GEOMAR Helmholtz-Zentrum für Ozeanforschung Kiel, Düsternbrooker Weg 20, 24105 Kiel, Germany
Related authors
Sankirna D. Joge, Anoop S. Mahajan, Shrivardhan Hulswar, Christa A. Marandino, Martí Galí, Thomas G. Bell, and Rafel Simó
Biogeosciences, 21, 4439–4452, https://doi.org/10.5194/bg-21-4439-2024, https://doi.org/10.5194/bg-21-4439-2024, 2024
Short summary
Short summary
Dimethyl sulfide (DMS) is the largest natural source of sulfur in the atmosphere and leads to the formation of cloud condensation nuclei. DMS emission and quantification of its impacts have large uncertainties, but a detailed study on the emissions and drivers of their uncertainty is missing to date. The emissions are usually calculated from the seawater DMS concentrations and a flux parameterization. Here we quantify the differences in DMS seawater products, which can affect DMS fluxes.
Sankirna D. Joge, Anoop S. Mahajan, Shrivardhan Hulswar, Christa A. Marandino, Martí Galí, Thomas G. Bell, Mingxi Yang, and Rafel Simó
Biogeosciences, 21, 4453–4467, https://doi.org/10.5194/bg-21-4453-2024, https://doi.org/10.5194/bg-21-4453-2024, 2024
Short summary
Short summary
Dimethyl sulfide (DMS) is the largest natural source of sulfur in the atmosphere and leads to the formation of cloud condensation nuclei. DMS emissions and quantification of their impacts have large uncertainties, but a detailed study on the range of emissions and drivers of their uncertainty is missing to date. The emissions are calculated from the seawater DMS concentrations and a flux parameterization. Here we quantify the differences in the effect of flux parameterizations used in models.
Li Zhou, Dennis Booge, Miming Zhang, and Christa A. Marandino
Biogeosciences, 19, 5021–5040, https://doi.org/10.5194/bg-19-5021-2022, https://doi.org/10.5194/bg-19-5021-2022, 2022
Short summary
Short summary
Trace gas air–sea exchange exerts an important control on air quality and climate, especially in the Southern Ocean (SO). Almost all of the measurements there are skewed to summer, but it is essential to expand our measurement database over greater temporal and spatial scales. Therefore, we report measured concentrations of dimethylsulfide (DMS, as well as related sulfur compounds) and isoprene in the Atlantic sector of the SO. The observations of isoprene are the first in the winter in the SO.
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
Short summary
Short summary
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.
Yanan Zhao, Dennis Booge, Christa A. Marandino, Cathleen Schlundt, Astrid Bracher, Elliot L. Atlas, Jonathan Williams, and Hermann W. Bange
Biogeosciences, 19, 701–714, https://doi.org/10.5194/bg-19-701-2022, https://doi.org/10.5194/bg-19-701-2022, 2022
Short summary
Short summary
We present here, for the first time, simultaneously measured dimethylsulfide (DMS) seawater concentrations and DMS atmospheric mole fractions from the Peruvian upwelling region during two cruises in December 2012 and October 2015. Our results indicate low oceanic DMS concentrations and atmospheric DMS molar fractions in surface waters and the atmosphere, respectively. In addition, the Peruvian upwelling region was identified as an insignificant source of DMS emissions during both periods.
Sinikka T. Lennartz, Michael Gauss, Marc von Hobe, and Christa A. Marandino
Earth Syst. Sci. Data, 13, 2095–2110, https://doi.org/10.5194/essd-13-2095-2021, https://doi.org/10.5194/essd-13-2095-2021, 2021
Short summary
Short summary
This study provides a marine emission inventory for the sulphur gases carbonyl sulphide (OCS) and carbon disulphide (CS2), derived from a numerical model of the surface ocean at monthly resolution for the period 2000–2019. Comparison with a database of seaborne observations reveals very good agreement for OCS. Interannual variability in both gases seems to be mainly driven by the amount of chromophoric dissolved organic matter present in surface water.
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
Short summary
Short summary
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.
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
Short summary
Short summary
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.
Alexander Zavarsky and Christa A. Marandino
Atmos. Chem. Phys., 19, 1819–1834, https://doi.org/10.5194/acp-19-1819-2019, https://doi.org/10.5194/acp-19-1819-2019, 2019
Short summary
Short summary
Wind–wave interaction can suppress gas transfer between the atmosphere and the ocean. Using a global wave model we investigate the impact of this interaction on the global gas transfer of CO2 and DMS. We also investigate the impact on of gas transfer limitation on two commonly used gas transfer velocity parameterizations.
Dennis Booge, Cathleen Schlundt, Astrid Bracher, Sonja Endres, Birthe Zäncker, and Christa A. Marandino
Biogeosciences, 15, 649–667, https://doi.org/10.5194/bg-15-649-2018, https://doi.org/10.5194/bg-15-649-2018, 2018
Short summary
Short summary
Our isoprene data from field measurements in the mixed layer from the Indian Ocean and the eastern Pacific Ocean show that the ability of different phytoplankton functional types to produce isoprene seems to be mainly influenced by light, ocean temperature, salinity, and nutrients. By calculating in-field isoprene production rates, we demonstrate that an additional loss is needed to explain the measured isoprene concentration, which is potentially due to degradation or consumption by bacteria.
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
Short summary
Short summary
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.
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
Short summary
Short summary
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.
Dennis Booge, Christa A. Marandino, Cathleen Schlundt, Paul I. Palmer, Michael Schlundt, Elliot L. Atlas, Astrid Bracher, Eric S. Saltzman, and Douglas W. R. Wallace
Atmos. Chem. Phys., 16, 11807–11821, https://doi.org/10.5194/acp-16-11807-2016, https://doi.org/10.5194/acp-16-11807-2016, 2016
Short summary
Short summary
Isoprene, a biogenic trace gas, is an important precursor of secondary organic aerosol/cloud condensation nuclei. Here, we use isoprene and related field measurements from three different ocean data sets together with remotely sensed satellite data to model global marine isoprene emissions. Our findings suggest that there is at least one missing oceanic source of isoprene and possibly other unknown factors in the ocean or atmosphere influencing the atmospheric values.
Lothar Stramma, Tim Fischer, Damian S. Grundle, Gerd Krahmann, Hermann W. Bange, and Christa A. Marandino
Ocean Sci., 12, 861–873, https://doi.org/10.5194/os-12-861-2016, https://doi.org/10.5194/os-12-861-2016, 2016
Short summary
Short summary
Results from a research cruise on R/V Sonne to the eastern tropical Pacific in October 2015 during the 2015–2016 El Niño show the transition of current, hydrographic, and nutrient conditions to El Niño conditions in the eastern tropical Pacific in October 2015. Although in early 2015 the El Niño was strong and in October 2015 showed a clear El Niño influence on the EUC, in the eastern tropical Pacific the measurements only showed developing El Niño water mass distributions.
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
Short summary
Short summary
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.
T. G. Bell, W. De Bruyn, C. A. Marandino, S. D. Miller, C. S. Law, M. J. Smith, and E. S. Saltzman
Atmos. Chem. Phys., 15, 1783–1794, https://doi.org/10.5194/acp-15-1783-2015, https://doi.org/10.5194/acp-15-1783-2015, 2015
C. Zindler, A. Bracher, C. A. Marandino, B. Taylor, E. Torrecilla, A. Kock, and H. W. Bange
Biogeosciences, 10, 3297–3311, https://doi.org/10.5194/bg-10-3297-2013, https://doi.org/10.5194/bg-10-3297-2013, 2013
Gesa Schulz, Kirstin Dähnke, Tina Sanders, Jan Penopp, Hermann W. Bange, Rena Czeschel, and Birgit Gaye
EGUsphere, https://doi.org/10.5194/egusphere-2025-1660, https://doi.org/10.5194/egusphere-2025-1660, 2025
This preprint is open for discussion and under review for Biogeosciences (BG).
Short summary
Short summary
Oxygen minimum zones (OMZs) are low-oxygen ocean areas that deplete nitrogen, a key marine nutrient. Understanding nitrogen cycling in OMZs is crucial for the global nitrogen cycle. This study examined nitrogen cycling in the OMZ of the Bay of Bengal and East Equatorial Indian Ocean, revealing limited mixing between both regions. Surface phytoplankton consumes nitrate, while deeper nitrification recycles nitrogen. In the BoB’s OMZ (100–300 m), nitrogen loss likely occurs via anammox.
Matthew Toohey, Yue Jia, Sujan Khanal, and Susann Tegtmeier
Atmos. Chem. Phys., 25, 3821–3839, https://doi.org/10.5194/acp-25-3821-2025, https://doi.org/10.5194/acp-25-3821-2025, 2025
Short summary
Short summary
The climate impact of volcanic eruptions depends in part on how long aerosols spend in the stratosphere. We develop a conceptual model for stratospheric aerosol lifetime in terms of production and decay timescales, as well as a lag between injection and decay. We find residence time depends strongly on injection height in the lower stratosphere. We show that the lifetime of stratospheric aerosol from the 1991 Pinatubo eruption is around 22 months, significantly longer than is commonly reported.
Shenglong Zhang, Jiao Chen, Jonathon S. Wright, Sean M. Davis, Jie Gao, Paul Konopka, Ninghui Li, Mengqian Lu, Susann Tegtmeier, Xiaolu Yan, Guang J. Zhang, and Nuanliang Zhu
EGUsphere, https://doi.org/10.5194/egusphere-2025-543, https://doi.org/10.5194/egusphere-2025-543, 2025
Short summary
Short summary
This study examines water vapor changes in the upper atmosphere above the Asian summer monsoon using satellite data and climate models. Three key patterns of variability were identified: year-to-year changes, and two shifting distributions driven by weather and monsoon dynamics. Despite uncertainties, modern models are improving in capturing these processes. This enhances understanding of water vapor’s role in the upper atmosphere.
Tómas Zoëga, Trude Storelvmo, and Kirstin Krüger
Atmos. Chem. Phys., 25, 2989–3010, https://doi.org/10.5194/acp-25-2989-2025, https://doi.org/10.5194/acp-25-2989-2025, 2025
Short summary
Short summary
We use an Earth system model to systematically investigate the climate response to high-latitude effusive volcanic eruptions as a function of eruption season and size, with a focus on the Arctic. We find that different seasons strongly modulate the climate response, with Arctic surface warming observed in winter and cooling in summer. Additionally, as eruptions increase in terms of sulfur dioxide emissions, the climate response becomes increasingly insensitive to variations in emission strength.
Mona Zolghadrshojaee, Susann Tegtmeier, Sean M. Davis, Robin Pilch Kedzierski, and Leopold Haimberger
EGUsphere, https://doi.org/10.5194/egusphere-2025-82, https://doi.org/10.5194/egusphere-2025-82, 2025
Short summary
Short summary
The tropical tropopause layer (TTL) is a crucial region where the troposphere transitions into the stratosphere, influencing air mass transport. This study examines temperature trends in the TTL and lower stratosphere using data from weather balloons, satellites, and reanalysis datasets. We found cooling trends in the TTL from 1980–2001, followed by warming from 2002–2023. These shifts are linked to changes in atmospheric circulation and impact water vapor transport into the stratosphere.
Kimberlee Dubé, Susann Tegtmeier, Felix Ploeger, and Kaley A. Walker
Atmos. Chem. Phys., 25, 1433–1447, https://doi.org/10.5194/acp-25-1433-2025, https://doi.org/10.5194/acp-25-1433-2025, 2025
Short summary
Short summary
The transport rate of air in the stratosphere has changed in response to human emissions of greenhouse gases and ozone-depleting substances. This transport rate can be approximated using measurements of long-lived trace gases. We use observations and model results to derive anomalies and trends in the mean rate of stratospheric air transport. We find that air in the Northern Hemisphere aged by up to 0.3 years per decade relative to air in the Southern Hemisphere over 2004–2017.
Jasna V. Pittman, Bruce C. Daube, Steven C. Wofsy, Elliot L. Atlas, Maria A. Navarro, Eric J. Hintsa, Fred L. Moore, Geoff S. Dutton, James W. Elkins, Troy D. Thornberry, Andrew W. Rollins, Eric J. Jensen, Thaopaul Bui, Jonathan M. Dean-Day, and Leonhard Pfister
EGUsphere, https://doi.org/10.5194/egusphere-2024-3832, https://doi.org/10.5194/egusphere-2024-3832, 2024
Short summary
Short summary
Wildfires emit aerosols and precursors that once in the stratosphere could initiate stratospheric ozone loss. The Airborne Tropical TRopopause EXperiment campaign sampled the western Pacific, the dominant longitudes where surface air lofted by convection enters the global stratosphere. Aircraft measurements provided evidence of persistent pollution layers of biomass burning character at these longitudes in the lower stratosphere, largely originating from distant fires over Africa and Indonesia.
Johnathan Daniel Maxey, Neil D. Hartstein, Hermann W. Bange, and Moritz Müller
Biogeosciences, 21, 5613–5637, https://doi.org/10.5194/bg-21-5613-2024, https://doi.org/10.5194/bg-21-5613-2024, 2024
Short summary
Short summary
The distribution of N2O in fjord-like estuaries is poorly described in the Southern Hemisphere. Our study describes N2O distribution and its drivers in one such system in Macquarie Harbour, Tasmania. Water samples were collected seasonally in 2022 and 2023. Results show the system removes atmospheric N2O when river flow is high, whereas the system emits N2O when the river flow is low. N2O generated in basins is intercepted by the surface water and exported to the ocean during high river flow.
Ryan Hossaini, David Sherry, Zihao Wang, Martyn P. Chipperfield, Wuhu Feng, David E. Oram, Karina E. Adcock, Stephen A. Montzka, Isobel J. Simpson, Andrea Mazzeo, Amber A. Leeson, Elliot Atlas, and Charles C.-K. Chou
Atmos. Chem. Phys., 24, 13457–13475, https://doi.org/10.5194/acp-24-13457-2024, https://doi.org/10.5194/acp-24-13457-2024, 2024
Short summary
Short summary
DCE (1,2-dichloroethane) is an industrial chemical used to produce PVC (polyvinyl chloride). We analysed DCE production data to estimate global DCE emissions (2002–2020). The emissions were included in an atmospheric model and evaluated by comparing simulated DCE to DCE measurements in the troposphere. We show that DCE contributes ozone-depleting Cl to the stratosphere and that this has increased with increasing DCE emissions. DCE’s impact on stratospheric O3 is currently small but non-zero.
Kimberlee Dubé, Susann Tegtmeier, Adam Bourassa, Daniel Zawada, Douglas Degenstein, William Randel, Sean Davis, Michael Schwartz, Nathaniel Livesey, and Anne Smith
Atmos. Chem. Phys., 24, 12925–12941, https://doi.org/10.5194/acp-24-12925-2024, https://doi.org/10.5194/acp-24-12925-2024, 2024
Short summary
Short summary
Greenhouse gas emissions that warm the troposphere also result in stratospheric cooling. The cooling rate is difficult to quantify above 35 km due to a deficit of long-term observational data with high vertical resolution in this region. We use satellite observations from several instruments, including a new temperature product from OSIRIS, to show that the upper stratosphere, from 35–60 km, cooled by 0.5 to 1 K per decade over 2005–2021 and by 0.6 K per decade over 1979–2021.
Sankirna D. Joge, Anoop S. Mahajan, Shrivardhan Hulswar, Christa A. Marandino, Martí Galí, Thomas G. Bell, and Rafel Simó
Biogeosciences, 21, 4439–4452, https://doi.org/10.5194/bg-21-4439-2024, https://doi.org/10.5194/bg-21-4439-2024, 2024
Short summary
Short summary
Dimethyl sulfide (DMS) is the largest natural source of sulfur in the atmosphere and leads to the formation of cloud condensation nuclei. DMS emission and quantification of its impacts have large uncertainties, but a detailed study on the emissions and drivers of their uncertainty is missing to date. The emissions are usually calculated from the seawater DMS concentrations and a flux parameterization. Here we quantify the differences in DMS seawater products, which can affect DMS fluxes.
Sankirna D. Joge, Anoop S. Mahajan, Shrivardhan Hulswar, Christa A. Marandino, Martí Galí, Thomas G. Bell, Mingxi Yang, and Rafel Simó
Biogeosciences, 21, 4453–4467, https://doi.org/10.5194/bg-21-4453-2024, https://doi.org/10.5194/bg-21-4453-2024, 2024
Short summary
Short summary
Dimethyl sulfide (DMS) is the largest natural source of sulfur in the atmosphere and leads to the formation of cloud condensation nuclei. DMS emissions and quantification of their impacts have large uncertainties, but a detailed study on the range of emissions and drivers of their uncertainty is missing to date. The emissions are calculated from the seawater DMS concentrations and a flux parameterization. Here we quantify the differences in the effect of flux parameterizations used in models.
Riel Carlo O. Ingeniero, Gesa Schulz, and Hermann W. Bange
Biogeosciences, 21, 3425–3440, https://doi.org/10.5194/bg-21-3425-2024, https://doi.org/10.5194/bg-21-3425-2024, 2024
Short summary
Short summary
Our research is the first to measure dissolved NO concentrations in temperate estuarine waters, providing insights into its distribution under varying conditions and enhancing our understanding of its production processes. Dissolved NO was supersaturated in the Elbe Estuary, indicating that it is a source of atmospheric NO. The observed distribution of dissolved NO most likely resulted from nitrification.
Andrea E. Gordon, Cameron R. Homeyer, Jessica B. Smith, Rei Ueyama, Jonathan M. Dean-Day, Elliot L. Atlas, Kate Smith, Jasna V. Pittman, David S. Sayres, David M. Wilmouth, Apoorva Pandey, Jason M. St. Clair, Thomas F. Hanisco, Jennifer Hare, Reem A. Hannun, Steven Wofsy, Bruce C. Daube, and Stephen Donnelly
Atmos. Chem. Phys., 24, 7591–7608, https://doi.org/10.5194/acp-24-7591-2024, https://doi.org/10.5194/acp-24-7591-2024, 2024
Short summary
Short summary
In situ airborne observations of ongoing tropopause-overshooting convection and an above-anvil cirrus plume from the 31 May 2022 flight of the Dynamics and Chemistry of the Summer Stratosphere (DCOTSS) field campaign are examined. Upper troposphere and lower stratosphere composition changes are evaluated along with possible contributing dynamical and physical processes. Measurements reveal multiple changes in air mass composition and stratospheric hydration throughout the flight.
Mona Zolghadrshojaee, Susann Tegtmeier, Sean M. Davis, and Robin Pilch Kedzierski
Atmos. Chem. Phys., 24, 7405–7419, https://doi.org/10.5194/acp-24-7405-2024, https://doi.org/10.5194/acp-24-7405-2024, 2024
Short summary
Short summary
Satellite data challenge the idea of an overall cooling trend in the tropical tropopause layer. From 2002 to 2022, a warming trend was observed, diverging from earlier findings. Tropopause height changes indicate dynamic processes alongside radiative effects. Upper-tropospheric warming contrasts with lower-stratosphere temperatures. The study highlights the complex interplay of factors shaping temperature trends.
Dennis Booge, Jerry F. Tjiputra, Dirk J. L. Olivié, Birgit Quack, and Kirstin Krüger
Earth Syst. Dynam., 15, 801–816, https://doi.org/10.5194/esd-15-801-2024, https://doi.org/10.5194/esd-15-801-2024, 2024
Short summary
Short summary
Oceanic bromoform, produced by algae, is an important precursor of atmospheric bromine, highlighting the importance of implementing these emissions in climate models. The simulated mean oceanic concentrations align well with observations, while the mean atmospheric values are lower than the observed ones. Modelled annual mean emissions mostly occur from the sea to the air and are driven by oceanic concentrations, sea surface temperature, and wind speed, which depend on season and location.
Hanqin Tian, Naiqing Pan, Rona L. Thompson, Josep G. Canadell, Parvadha Suntharalingam, Pierre Regnier, Eric A. Davidson, Michael Prather, Philippe Ciais, Marilena Muntean, Shufen Pan, Wilfried Winiwarter, Sönke Zaehle, Feng Zhou, Robert B. Jackson, Hermann W. Bange, Sarah Berthet, Zihao Bian, Daniele Bianchi, Alexander F. Bouwman, Erik T. Buitenhuis, Geoffrey Dutton, Minpeng Hu, Akihiko Ito, Atul K. Jain, Aurich Jeltsch-Thömmes, Fortunat Joos, Sian Kou-Giesbrecht, Paul B. Krummel, Xin Lan, Angela Landolfi, Ronny Lauerwald, Ya Li, Chaoqun Lu, Taylor Maavara, Manfredi Manizza, Dylan B. Millet, Jens Mühle, Prabir K. Patra, Glen P. Peters, Xiaoyu Qin, Peter Raymond, Laure Resplandy, Judith A. Rosentreter, Hao Shi, Qing Sun, Daniele Tonina, Francesco N. Tubiello, Guido R. van der Werf, Nicolas Vuichard, Junjie Wang, Kelley C. Wells, Luke M. Western, Chris Wilson, Jia Yang, Yuanzhi Yao, Yongfa You, and Qing Zhu
Earth Syst. Sci. Data, 16, 2543–2604, https://doi.org/10.5194/essd-16-2543-2024, https://doi.org/10.5194/essd-16-2543-2024, 2024
Short summary
Short summary
Atmospheric concentrations of nitrous oxide (N2O), a greenhouse gas 273 times more potent than carbon dioxide, have increased by 25 % since the preindustrial period, with the highest observed growth rate in 2020 and 2021. This rapid growth rate has primarily been due to a 40 % increase in anthropogenic emissions since 1980. Observed atmospheric N2O concentrations in recent years have exceeded the worst-case climate scenario, underscoring the importance of reducing anthropogenic N2O emissions.
Zhihong Zhuo, Herman F. Fuglestvedt, Matthew Toohey, and Kirstin Krüger
Atmos. Chem. Phys., 24, 6233–6249, https://doi.org/10.5194/acp-24-6233-2024, https://doi.org/10.5194/acp-24-6233-2024, 2024
Short summary
Short summary
This work simulated volcanic eruptions with varied eruption source parameters under different initial conditions with a fully coupled Earth system model. We show that initial atmospheric conditions control the meridional distribution of volcanic volatiles and modulate volcanic forcing and subsequent climate and environmental impacts of tropical and Northern Hemisphere extratropical eruptions. This highlights the potential for predicting these impacts as early as the first post-eruption month.
Bjorn Stevens, Stefan Adami, Tariq Ali, Hartwig Anzt, Zafer Aslan, Sabine Attinger, Jaana Bäck, Johanna Baehr, Peter Bauer, Natacha Bernier, Bob Bishop, Hendryk Bockelmann, Sandrine Bony, Guy Brasseur, David N. Bresch, Sean Breyer, Gilbert Brunet, Pier Luigi Buttigieg, Junji Cao, Christelle Castet, Yafang Cheng, Ayantika Dey Choudhury, Deborah Coen, Susanne Crewell, Atish Dabholkar, Qing Dai, Francisco Doblas-Reyes, Dale Durran, Ayoub El Gaidi, Charlie Ewen, Eleftheria Exarchou, Veronika Eyring, Florencia Falkinhoff, David Farrell, Piers M. Forster, Ariane Frassoni, Claudia Frauen, Oliver Fuhrer, Shahzad Gani, Edwin Gerber, Debra Goldfarb, Jens Grieger, Nicolas Gruber, Wilco Hazeleger, Rolf Herken, Chris Hewitt, Torsten Hoefler, Huang-Hsiung Hsu, Daniela Jacob, Alexandra Jahn, Christian Jakob, Thomas Jung, Christopher Kadow, In-Sik Kang, Sarah Kang, Karthik Kashinath, Katharina Kleinen-von Königslöw, Daniel Klocke, Uta Kloenne, Milan Klöwer, Chihiro Kodama, Stefan Kollet, Tobias Kölling, Jenni Kontkanen, Steve Kopp, Michal Koran, Markku Kulmala, Hanna Lappalainen, Fakhria Latifi, Bryan Lawrence, June Yi Lee, Quentin Lejeun, Christian Lessig, Chao Li, Thomas Lippert, Jürg Luterbacher, Pekka Manninen, Jochem Marotzke, Satoshi Matsouoka, Charlotte Merchant, Peter Messmer, Gero Michel, Kristel Michielsen, Tomoki Miyakawa, Jens Müller, Ramsha Munir, Sandeep Narayanasetti, Ousmane Ndiaye, Carlos Nobre, Achim Oberg, Riko Oki, Tuba Özkan-Haller, Tim Palmer, Stan Posey, Andreas Prein, Odessa Primus, Mike Pritchard, Julie Pullen, Dian Putrasahan, Johannes Quaas, Krishnan Raghavan, Venkatachalam Ramaswamy, Markus Rapp, Florian Rauser, Markus Reichstein, Aromar Revi, Sonakshi Saluja, Masaki Satoh, Vera Schemann, Sebastian Schemm, Christina Schnadt Poberaj, Thomas Schulthess, Cath Senior, Jagadish Shukla, Manmeet Singh, Julia Slingo, Adam Sobel, Silvina Solman, Jenna Spitzer, Philip Stier, Thomas Stocker, Sarah Strock, Hang Su, Petteri Taalas, John Taylor, Susann Tegtmeier, Georg Teutsch, Adrian Tompkins, Uwe Ulbrich, Pier-Luigi Vidale, Chien-Ming Wu, Hao Xu, Najibullah Zaki, Laure Zanna, Tianjun Zhou, and Florian Ziemen
Earth Syst. Sci. Data, 16, 2113–2122, https://doi.org/10.5194/essd-16-2113-2024, https://doi.org/10.5194/essd-16-2113-2024, 2024
Short summary
Short summary
To manage Earth in the Anthropocene, new tools, new institutions, and new forms of international cooperation will be required. Earth Virtualization Engines is proposed as an international federation of centers of excellence to empower all people to respond to the immense and urgent challenges posed by climate change.
Daniel Zawada, Kimberlee Dubé, Taran Warnock, Adam Bourassa, Susann Tegtmeier, and Douglas Degenstein
Atmos. Meas. Tech., 17, 1995–2010, https://doi.org/10.5194/amt-17-1995-2024, https://doi.org/10.5194/amt-17-1995-2024, 2024
Short summary
Short summary
There remain large uncertainties in long-term changes of stratospheric–atmospheric temperatures. We have produced a time series of more than 20 years of satellite-based temperature measurements from the OSIRIS instrument in the upper–middle stratosphere. The dataset is publicly available and intended to be used for a better understanding of changes in stratospheric temperatures.
Kimberlee Dubé, Susann Tegtmeier, Adam Bourassa, Daniel Zawada, Douglas Degenstein, Patrick E. Sheese, Kaley A. Walker, and William Randel
Atmos. Chem. Phys., 23, 13283–13300, https://doi.org/10.5194/acp-23-13283-2023, https://doi.org/10.5194/acp-23-13283-2023, 2023
Short summary
Short summary
This paper presents a technique for understanding the causes of long-term changes in stratospheric composition. By using N2O as a proxy for stratospheric circulation in the model used to calculated trends, it is possible to separate the effects of dynamics and chemistry on observed trace gas trends. We find that observed HCl increases are due to changes in the stratospheric circulation, as are O3 decreases above 30 hPa in the Northern Hemisphere.
Gesa Schulz, Tina Sanders, Yoana G. Voynova, Hermann W. Bange, and Kirstin Dähnke
Biogeosciences, 20, 3229–3247, https://doi.org/10.5194/bg-20-3229-2023, https://doi.org/10.5194/bg-20-3229-2023, 2023
Short summary
Short summary
Nitrous oxide (N2O) is an important greenhouse gas. However, N2O emissions from estuaries underlie significant uncertainties due to limited data availability and high spatiotemporal variability. We found the Elbe Estuary (Germany) to be a year-round source of N2O, with the highest emissions in winter along with high nitrogen loads. However, in spring and summer, N2O emissions did not decrease alongside lower nitrogen loads because organic matter fueled in situ N2O production along the estuary.
Guanlin Li, Damian L. Arévalo-Martínez, Riel Carlo O. Ingeniero, and Hermann W. Bange
EGUsphere, https://doi.org/10.5194/egusphere-2023-771, https://doi.org/10.5194/egusphere-2023-771, 2023
Preprint archived
Short summary
Short summary
Dissolved carbon monoxide (CO) surface concentrations were first measured at 14 stations in the Ria Formosa Lagoon system in May 2021. Ria Formosa was a source of atmospheric CO. Microbial consumption accounted for 83 % of the CO production. The results of a 48-hour irradiation experiment with aquaculture effluent water indicated that aquaculture facilities in the Ria Formosa Lagoon seem to be a negligible source of atmospheric CO.
Hanna I. Campen, Damian L. Arévalo-Martínez, and Hermann W. Bange
Biogeosciences, 20, 1371–1379, https://doi.org/10.5194/bg-20-1371-2023, https://doi.org/10.5194/bg-20-1371-2023, 2023
Short summary
Short summary
Carbon monoxide (CO) is a climate-relevant trace gas emitted from the ocean. However, oceanic CO cycling is understudied. Results from incubation experiments conducted in the Fram Strait (Arctic Ocean) indicated that (i) pH did not affect CO cycling and (ii) enhanced CO production and consumption were positively correlated with coloured dissolved organic matter and nitrate concentrations. This suggests microbial CO uptake to be the driving factor for CO cycling in the Arctic Ocean.
Damian L. Arévalo-Martínez, Amir Haroon, Hermann W. Bange, Ercan Erkul, Marion Jegen, Nils Moosdorf, Jens Schneider von Deimling, Christian Berndt, Michael Ernst Böttcher, Jasper Hoffmann, Volker Liebetrau, Ulf Mallast, Gudrun Massmann, Aaron Micallef, Holly A. Michael, Hendrik Paasche, Wolfgang Rabbel, Isaac Santos, Jan Scholten, Katrin Schwalenberg, Beata Szymczycha, Ariel T. Thomas, Joonas J. Virtasalo, Hannelore Waska, and Bradley A. Weymer
Biogeosciences, 20, 647–662, https://doi.org/10.5194/bg-20-647-2023, https://doi.org/10.5194/bg-20-647-2023, 2023
Short summary
Short summary
Groundwater flows at the land–ocean transition and the extent of freshened groundwater below the seafloor are increasingly relevant in marine sciences, both because they are a highly uncertain term of biogeochemical budgets and due to the emerging interest in the latter as a resource. Here, we discuss our perspectives on future research directions to better understand land–ocean connectivity through groundwater and its potential responses to natural and human-induced environmental changes.
Evelien van Dijk, Ingar Mørkestøl Gundersen, Anna de Bode, Helge Høeg, Kjetil Loftsgarden, Frode Iversen, Claudia Timmreck, Johann Jungclaus, and Kirstin Krüger
Clim. Past, 19, 357–398, https://doi.org/10.5194/cp-19-357-2023, https://doi.org/10.5194/cp-19-357-2023, 2023
Short summary
Short summary
The mid-6th century was one of the coldest periods of the last 2000 years as characterized by great societal changes. Here, we study the effect of the volcanic double event in 536 CE and 540 CE on climate and society in southern Norway. The combined climate and growing degree day models and high-resolution pollen and archaeological records reveal that the northern and western sites are vulnerable to crop failure with possible abandonment of farms, whereas the southeastern site is more resilient.
Markus Jesswein, Rafael P. Fernandez, Lucas Berná, Alfonso Saiz-Lopez, Jens-Uwe Grooß, Ryan Hossaini, Eric C. Apel, Rebecca S. Hornbrook, Elliot L. Atlas, Donald R. Blake, Stephen Montzka, Timo Keber, Tanja Schuck, Thomas Wagenhäuser, and Andreas Engel
Atmos. Chem. Phys., 22, 15049–15070, https://doi.org/10.5194/acp-22-15049-2022, https://doi.org/10.5194/acp-22-15049-2022, 2022
Short summary
Short summary
This study presents the global and seasonal distribution of the two major brominated short-lived substances CH2Br2 and CHBr3 in the upper troposphere and lower stratosphere based on observations from several aircraft campaigns. They show similar seasonality for both hemispheres, except in the respective hemispheric autumn lower stratosphere. A comparison with the TOMCAT and CAM-Chem models shows good agreement in the annual mean but larger differences in the seasonal consideration.
Shih-Wei Fang, Claudia Timmreck, Johann Jungclaus, Kirstin Krüger, and Hauke Schmidt
Earth Syst. Dynam., 13, 1535–1555, https://doi.org/10.5194/esd-13-1535-2022, https://doi.org/10.5194/esd-13-1535-2022, 2022
Short summary
Short summary
The early 19th century was the coldest period over the past 500 years, when strong tropical volcanic events and a solar minimum coincided. This study quantifies potential surface cooling from the solar and volcanic forcing in the early 19th century with large ensemble simulations, and identifies the regions that their impacts cannot be simply additive. The cooling perspective of Arctic amplification exists in both solar and post-volcano period with the albedo feedback as the main contribution.
Li Zhou, Dennis Booge, Miming Zhang, and Christa A. Marandino
Biogeosciences, 19, 5021–5040, https://doi.org/10.5194/bg-19-5021-2022, https://doi.org/10.5194/bg-19-5021-2022, 2022
Short summary
Short summary
Trace gas air–sea exchange exerts an important control on air quality and climate, especially in the Southern Ocean (SO). Almost all of the measurements there are skewed to summer, but it is essential to expand our measurement database over greater temporal and spatial scales. Therefore, we report measured concentrations of dimethylsulfide (DMS, as well as related sulfur compounds) and isoprene in the Atlantic sector of the SO. The observations of isoprene are the first in the winter in the SO.
Sonja Gindorf, Hermann W. Bange, Dennis Booge, and Annette Kock
Biogeosciences, 19, 4993–5006, https://doi.org/10.5194/bg-19-4993-2022, https://doi.org/10.5194/bg-19-4993-2022, 2022
Short summary
Short summary
Methane is a climate-relevant greenhouse gas which is emitted to the atmosphere from coastal areas such as the Baltic Sea. We measured the methane concentration in the water column of the western Kiel Bight. Methane concentrations were higher in September than in June. We found no relationship between the 2018 European heatwave and methane concentrations. Our results show that the methane distribution in the water column is strongly affected by temporal and spatial variabilities.
Kristof Bognar, Susann Tegtmeier, Adam Bourassa, Chris Roth, Taran Warnock, Daniel Zawada, and Doug Degenstein
Atmos. Chem. Phys., 22, 9553–9569, https://doi.org/10.5194/acp-22-9553-2022, https://doi.org/10.5194/acp-22-9553-2022, 2022
Short summary
Short summary
We quantify recent changes in stratospheric ozone (outside the polar regions) using a combination of three satellite datasets. We find that upper stratospheric ozone have increased significantly since 2000, although the recovery shows an unexpected pause in the Northern Hemisphere. Combined with the likely decrease in ozone in the lower stratosphere, this presents an interesting challenge for predicting the future of the ozone layer.
Evelien van Dijk, Johann Jungclaus, Stephan Lorenz, Claudia Timmreck, and Kirstin Krüger
Clim. Past, 18, 1601–1623, https://doi.org/10.5194/cp-18-1601-2022, https://doi.org/10.5194/cp-18-1601-2022, 2022
Short summary
Short summary
A double volcanic eruption in 536 and 540 CE caused one of the coldest decades during the last 2000 years. We analyzed new climate model simulations from that period and 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; this in turn leads to a surface cooling up to 20 years after the eruptions.
Yue Jia, Birgit Quack, Robert D. Kinley, Ignacio Pisso, and Susann Tegtmeier
Atmos. Chem. Phys., 22, 7631–7646, https://doi.org/10.5194/acp-22-7631-2022, https://doi.org/10.5194/acp-22-7631-2022, 2022
Short summary
Short summary
In this study, we assessed the potential risks of bromoform released from Asparagopsis farming near Australia for the stratospheric ozone layer by analyzing different cultivation scenarios. We conclude that the intended operation of Asparagopsis seaweed cultivation farms with an annual yield to meet the needs of 50 % of feedlots and cattle in either open-ocean or terrestrial cultures in Australia will not impact the ozone layer under normal operating conditions.
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
Short summary
Short summary
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.
Eric A. Ray, Elliot L. Atlas, Sue Schauffler, Sofia Chelpon, Laura Pan, Harald Bönisch, and Karen H. Rosenlof
Atmos. Chem. Phys., 22, 6539–6558, https://doi.org/10.5194/acp-22-6539-2022, https://doi.org/10.5194/acp-22-6539-2022, 2022
Short summary
Short summary
The movement of air masses and the trace gases they contain from the Earth’s surface into the upper troposphere and lower stratosphere (UTLS) can have important implications for the radiative and chemical balance of the atmosphere. In this study we build on recent techniques and use new ones to estimate a range of transport diagnostics based on simultaneously measured trace gases in the UTLS during the monsoon season in North America.
Guangyu Liu, Toshihiko Hirooka, Nawo Eguchi, and Kirstin Krüger
Atmos. Chem. Phys., 22, 3493–3505, https://doi.org/10.5194/acp-22-3493-2022, https://doi.org/10.5194/acp-22-3493-2022, 2022
Short summary
Short summary
The sudden stratospheric warming (SSW) event that occurred in September 2019 in the Southern Hemisphere was analyzed. A large warming and decelerated westerly winds were observed in the southern polar region. Since a reversal from westerly to easterly winds did not take place SSW2019 was classified as a minor SSW. The total wave forcing and the contribution from PW1 were larger in 2019. The strong and long-lasting planetary-scale waves with zonal wavenumber 1 played a role in SSW2019.
Yanan Zhao, Dennis Booge, Christa A. Marandino, Cathleen Schlundt, Astrid Bracher, Elliot L. Atlas, Jonathan Williams, and Hermann W. Bange
Biogeosciences, 19, 701–714, https://doi.org/10.5194/bg-19-701-2022, https://doi.org/10.5194/bg-19-701-2022, 2022
Short summary
Short summary
We present here, for the first time, simultaneously measured dimethylsulfide (DMS) seawater concentrations and DMS atmospheric mole fractions from the Peruvian upwelling region during two cruises in December 2012 and October 2015. Our results indicate low oceanic DMS concentrations and atmospheric DMS molar fractions in surface waters and the atmosphere, respectively. In addition, the Peruvian upwelling region was identified as an insignificant source of DMS emissions during both periods.
Charitha Pattiaratchi, Mirjam van der Mheen, Cathleen Schlundt, Bhavani E. Narayanaswamy, Appalanaidu Sura, Sara Hajbane, Rachel White, Nimit Kumar, Michelle Fernandes, and Sarath Wijeratne
Ocean Sci., 18, 1–28, https://doi.org/10.5194/os-18-1-2022, https://doi.org/10.5194/os-18-1-2022, 2022
Short summary
Short summary
The Indian Ocean receives a large proportion of plastics, but very few studies have addressed the sources, transport pathways, and sinks. There is a scarcity of observational data for the Indian Ocean. Most plastic sources are derived from rivers, although the amount derived from fishing activity (ghost nets, discarded ropes) is unknown. The unique topographic features of the Indian Ocean that create the monsoons and reversing currents have a large influence on the transport and sinks.
Wangwang Ye, Hermann W. Bange, Damian L. Arévalo-Martínez, Hailun He, Yuhong Li, Jianwen Wen, Jiexia Zhang, Jian Liu, Man Wu, and Liyang Zhan
Biogeosciences Discuss., https://doi.org/10.5194/bg-2021-334, https://doi.org/10.5194/bg-2021-334, 2022
Manuscript not accepted for further review
Short summary
Short summary
CH4 is the second important greenhouse gas after CO2. We show that CH4 consumption and sea-ice melting influence the CH4 distribution in the Ross Sea (Southern Ocean), causing undersaturation and net uptake of CH4 during summertime. This study confirms the capability of surface water in the high-latitude Southern Ocean regions to take up atmospheric CH4 which, in turn, will help to improve predictions of how CH4 release/uptake from the ocean will develop when sea-ice retreats in the future.
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
Short summary
Short summary
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.
Sinikka T. Lennartz, Michael Gauss, Marc von Hobe, and Christa A. Marandino
Earth Syst. Sci. Data, 13, 2095–2110, https://doi.org/10.5194/essd-13-2095-2021, https://doi.org/10.5194/essd-13-2095-2021, 2021
Short summary
Short summary
This study provides a marine emission inventory for the sulphur gases carbonyl sulphide (OCS) and carbon disulphide (CS2), derived from a numerical model of the surface ocean at monthly resolution for the period 2000–2019. Comparison with a database of seaborne observations reveals very good agreement for OCS. Interannual variability in both gases seems to be mainly driven by the amount of chromophoric dissolved organic matter present in surface water.
Michaela I. Hegglin, Susann Tegtmeier, John Anderson, Adam E. Bourassa, Samuel Brohede, Doug Degenstein, Lucien Froidevaux, Bernd Funke, John Gille, Yasuko Kasai, Erkki T. Kyrölä, Jerry Lumpe, Donal Murtagh, Jessica L. Neu, Kristell Pérot, Ellis E. Remsberg, Alexei Rozanov, Matthew Toohey, Joachim Urban, Thomas von Clarmann, Kaley A. Walker, Hsiang-Jui Wang, Carlo Arosio, Robert Damadeo, Ryan A. Fuller, Gretchen Lingenfelser, Christopher McLinden, Diane Pendlebury, Chris Roth, Niall J. Ryan, Christopher Sioris, Lesley Smith, and Katja Weigel
Earth Syst. Sci. Data, 13, 1855–1903, https://doi.org/10.5194/essd-13-1855-2021, https://doi.org/10.5194/essd-13-1855-2021, 2021
Short summary
Short summary
An overview of the SPARC Data Initiative is presented, to date the most comprehensive assessment of stratospheric composition measurements spanning 1979–2018. Measurements of 26 chemical constituents obtained from an international suite of space-based limb sounders were compiled into vertically resolved, zonal monthly mean time series. The quality and consistency of these gridded datasets are then evaluated using a climatological validation approach and a range of diagnostics.
Yanan Zhao, Cathleen Schlundt, Dennis Booge, and Hermann W. Bange
Biogeosciences, 18, 2161–2179, https://doi.org/10.5194/bg-18-2161-2021, https://doi.org/10.5194/bg-18-2161-2021, 2021
Short summary
Short summary
We present a unique and comprehensive time-series study of biogenic sulfur compounds in the southwestern Baltic Sea, from 2009 to 2018. Dimethyl sulfide is one of the key players regulating global climate change, as well as dimethylsulfoniopropionate and dimethyl sulfoxide. Their decadal trends did not follow increasing temperature but followed some algae group abundances at the Boknis Eck Time Series Station.
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
Short summary
Short summary
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.
Jin Ma, Linda M. J. Kooijmans, Ara Cho, Stephen A. Montzka, Norbert Glatthor, John R. Worden, Le Kuai, Elliot L. Atlas, and Maarten C. Krol
Atmos. Chem. Phys., 21, 3507–3529, https://doi.org/10.5194/acp-21-3507-2021, https://doi.org/10.5194/acp-21-3507-2021, 2021
Short summary
Short summary
Carbonyl sulfide is an important trace gas in the atmosphere and useful to estimating gross primary productivity in ecosystems, but its sources and sinks remain highly uncertain. Therefore, we applied inverse model system TM5-4DVAR to better constrain the global budget. Our finding is in line with earlier studies, pointing to missing sources in the tropics and more uptake in high latitudes. We also stress the necessity of more ground-based observations and satellite data assimilation in future.
Samuel T. Wilson, Alia N. Al-Haj, Annie Bourbonnais, Claudia Frey, Robinson W. Fulweiler, John D. Kessler, Hannah K. Marchant, Jana Milucka, Nicholas E. Ray, Parvadha Suntharalingam, Brett F. Thornton, Robert C. Upstill-Goddard, Thomas S. Weber, Damian L. Arévalo-Martínez, Hermann W. Bange, Heather M. Benway, Daniele Bianchi, Alberto V. Borges, Bonnie X. Chang, Patrick M. Crill, Daniela A. del Valle, Laura Farías, Samantha B. Joye, Annette Kock, Jabrane Labidi, Cara C. Manning, John W. Pohlman, Gregor Rehder, Katy J. Sparrow, Philippe D. Tortell, Tina Treude, David L. Valentine, Bess B. Ward, Simon Yang, and Leonid N. Yurganov
Biogeosciences, 17, 5809–5828, https://doi.org/10.5194/bg-17-5809-2020, https://doi.org/10.5194/bg-17-5809-2020, 2020
Short summary
Short summary
The oceans are a net source of the major greenhouse gases; however there has been little coordination of oceanic methane and nitrous oxide measurements. The scientific community has recently embarked on a series of capacity-building exercises to improve the interoperability of dissolved methane and nitrous oxide measurements. This paper derives from a workshop which discussed the challenges and opportunities for oceanic methane and nitrous oxide research in the near future.
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
Short summary
Short summary
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.
Xiao Ma, Mingshuang Sun, Sinikka T. Lennartz, and Hermann W. Bange
Biogeosciences, 17, 3427–3438, https://doi.org/10.5194/bg-17-3427-2020, https://doi.org/10.5194/bg-17-3427-2020, 2020
Short summary
Short summary
Monthly measurements of dissolved methane (CH4), a potent greenhouse gas, were conducted at Boknis Eck (BE), a time-series station in the southwestern Baltic Sea, from June 2006. In general CH4 concentrations increased with depth. High concentrations in the upper layer were linked to saline water inflow. Eckernförde Bay emitted CH4 to the atmosphere throughout the monitoring period. No significant trend was detected in CH4 concentrations or emissions during 2006–2017.
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
Short summary
Short summary
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.
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
Short summary
Short summary
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.
Claudia Frey, Hermann W. Bange, Eric P. Achterberg, Amal Jayakumar, Carolin R. Löscher, Damian L. Arévalo-Martínez, Elizabeth León-Palmero, Mingshuang Sun, Xin Sun, Ruifang C. Xie, Sergey Oleynik, and Bess B. Ward
Biogeosciences, 17, 2263–2287, https://doi.org/10.5194/bg-17-2263-2020, https://doi.org/10.5194/bg-17-2263-2020, 2020
Short summary
Short summary
The production of N2O via nitrification and denitrification associated with low-O2 waters is a major source of oceanic N2O. We investigated the regulation and dynamics of these processes with respect to O2 and organic matter inputs. The transcription of the key nitrification gene amoA rapidly responded to changes in O2 and strongly correlated with N2O production rates. N2O production by denitrification was clearly stimulated by organic carbon, implying that its supply controls N2O production.
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
Short summary
Short summary
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.
Carolin R. Löscher, Wiebke Mohr, Hermann W. Bange, and Donald E. Canfield
Biogeosciences, 17, 851–864, https://doi.org/10.5194/bg-17-851-2020, https://doi.org/10.5194/bg-17-851-2020, 2020
Short summary
Short summary
Oxygen minimum zones (OMZs) are ocean areas severely depleted in oxygen as a result of physical, chemical, and biological processes. Biologically, organic material is produced in the sea surface and exported to deeper waters, where it respires. In the Bay of Bengal (BoB), an OMZ is present, but there are traces of oxygen left. Our study now suggests that this is because one key process, nitrogen fixation, is absent in the BoB, thus preventing primary production and consecutive respiration.
Ye Tian, Gui-Peng Yang, Chun-Ying Liu, Pei-Feng Li, Hong-Tao Chen, and Hermann W. Bange
Ocean Sci., 16, 135–148, https://doi.org/10.5194/os-16-135-2020, https://doi.org/10.5194/os-16-135-2020, 2020
Short summary
Short summary
Nitric oxide (NO) could be produced by nitrite photolysis; the rates from dissolved nitrite in artificial seawater showed increasing trends with decreasing pH, increasing temperatures, and increasing salinity. However, NO photoproduction from the natural seawater samples did not show correlations with pH, water temperature, salinity, or dissolved nitrite concentrations in the western tropical North Pacific Ocean (WNTP). And there were other NO loss processes in the surface layer of WNTP.
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
Short summary
Short summary
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.
Thomas Holding, Ian G. Ashton, Jamie D. Shutler, Peter E. Land, Philip D. Nightingale, Andrew P. Rees, Ian Brown, Jean-Francois Piolle, Annette Kock, Hermann W. Bange, David K. Woolf, Lonneke Goddijn-Murphy, Ryan Pereira, Frederic Paul, Fanny Girard-Ardhuin, Bertrand Chapron, Gregor Rehder, Fabrice Ardhuin, and Craig J. Donlon
Ocean Sci., 15, 1707–1728, https://doi.org/10.5194/os-15-1707-2019, https://doi.org/10.5194/os-15-1707-2019, 2019
Short summary
Short summary
FluxEngine is an open-source software toolbox designed to allow for the easy and accurate calculation of air–sea gas fluxes. This article describes new functionality and capabilities, which include the ability to calculate fluxes for nitrous oxide and methane, optimisation for running FluxEngine on a stand-alone desktop computer, and extensive new features to support the in situ measurement community. Four research case studies are used to demonstrate these new features.
Ye Tian, Chao Xue, Chun-Ying Liu, Gui-Peng Yang, Pei-Feng Li, Wei-Hua Feng, and Hermann W. Bange
Biogeosciences, 16, 4485–4496, https://doi.org/10.5194/bg-16-4485-2019, https://doi.org/10.5194/bg-16-4485-2019, 2019
Short summary
Short summary
Nitric oxide (NO) seems to be widespread, with different functions in the marine ecosystem, but we know little about it. Concentrations of NO were in a range from below the limit of detection to 616 pmol L−1 at the surface and 482 pmol L−1 at the bottom of the Bohai and Yellow seas. The study region was a source of atmospheric NO. Net NO sea-to-air fluxes were much lower than NO photoproduction rates, implying that the NO produced in the mixed layer was rapidly consumed before entering the air.
Elizabeth Asher, Rebecca S. Hornbrook, Britton B. Stephens, Doug Kinnison, Eric J. Morgan, Ralph F. Keeling, Elliot L. Atlas, Sue M. Schauffler, Simone Tilmes, Eric A. Kort, Martin S. Hoecker-Martínez, Matt C. Long, Jean-François Lamarque, Alfonso Saiz-Lopez, Kathryn McKain, Colm Sweeney, Alan J. Hills, and Eric C. Apel
Atmos. Chem. Phys., 19, 14071–14090, https://doi.org/10.5194/acp-19-14071-2019, https://doi.org/10.5194/acp-19-14071-2019, 2019
Short summary
Short summary
Halogenated organic trace gases, which are a source of reactive halogens to the atmosphere, exert a disproportionately large influence on atmospheric chemistry and climate. This paper reports novel aircraft observations of halogenated compounds over the Southern Ocean in summer and evaluates hypothesized regional sources and emissions of these trace gases through their relationships to additional aircraft observations.
Hermann W. Bange, Chun Hock Sim, Daniel Bastian, Jennifer Kallert, Annette Kock, Aazani Mujahid, and Moritz Müller
Biogeosciences, 16, 4321–4335, https://doi.org/10.5194/bg-16-4321-2019, https://doi.org/10.5194/bg-16-4321-2019, 2019
Short summary
Short summary
Nitrous oxide (N2O) and methane (CH4) are atmospheric trace gases which play important roles in the climate and atmospheric chemistry of the Earth. However, little is known about their emissions from rivers and estuaries. To this end, concentrations of N2O and CH4 were measured during a seasonal study in six rivers and estuaries in northwestern Borneo. The concentrations of both gases were mainly driven by rainfall. The rivers and estuaries were an overall net source of atmospheric N2O and CH4.
Xiao Ma, Sinikka T. Lennartz, and Hermann W. Bange
Biogeosciences, 16, 4097–4111, https://doi.org/10.5194/bg-16-4097-2019, https://doi.org/10.5194/bg-16-4097-2019, 2019
Short summary
Short summary
Monthly measurements of nitrous oxide (N2O), a potent greenhouse gas and ozone depletion agent, were conducted at Boknis Eck (BE), a time series station in the southwestern Baltic Sea, since July 2005. Low N2O concentrations were observed in autumn and high in winter and early spring. Dissolved nutrients and oxygen played important roles in N2O distribution. Although we did not observe a significant N2O trend during 2005–2017, a decrease in N2O concentration and emission seems likely in future.
Eric J. Morgan, Jost V. Lavric, Damian L. Arévalo-Martínez, Hermann W. Bange, Tobias Steinhoff, Thomas Seifert, and Martin Heimann
Biogeosciences, 16, 4065–4084, https://doi.org/10.5194/bg-16-4065-2019, https://doi.org/10.5194/bg-16-4065-2019, 2019
Short summary
Short summary
Taking a 2-year atmospheric record of atmospheric oxygen and the greenhouse gases N2O, CO2, and CH4, made at a coastal site in the Namib Desert, we estimated the fluxes of these gases from upwelling events in the northern Benguela Current region. We compared these results with flux measurements made on a research vessel in the study area at the same time and found that the two approaches agreed well. The study region was a source of N2O, CO2, and CH4 to the atmosphere during upwelling events.
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
Short summary
Short summary
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
Short summary
Short summary
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.
Xin Chen, Dylan B. Millet, Hanwant B. Singh, Armin Wisthaler, Eric C. Apel, Elliot L. Atlas, Donald R. Blake, Ilann Bourgeois, Steven S. Brown, John D. Crounse, Joost A. de Gouw, Frank M. Flocke, Alan Fried, Brian G. Heikes, Rebecca S. Hornbrook, Tomas Mikoviny, Kyung-Eun Min, Markus Müller, J. Andrew Neuman, Daniel W. O'Sullivan, Jeff Peischl, Gabriele G. Pfister, Dirk Richter, James M. Roberts, Thomas B. Ryerson, Stephen R. Shertz, Chelsea R. Thompson, Victoria Treadaway, Patrick R. Veres, James Walega, Carsten Warneke, Rebecca A. Washenfelder, Petter Weibring, and Bin Yuan
Atmos. Chem. Phys., 19, 9097–9123, https://doi.org/10.5194/acp-19-9097-2019, https://doi.org/10.5194/acp-19-9097-2019, 2019
Short summary
Short summary
Volatile organic compounds (VOCs) affect air quality and modify the lifetimes of other pollutants. We combine a high-resolution 3-D atmospheric model with an ensemble of aircraft observations to perform an integrated analysis of the VOC budget over North America. We find that biogenic emissions provide the main source of VOC reactivity even in most major cities. Our findings point to key gaps in current models related to oxygenated VOCs and to the distribution of VOCs in the free troposphere.
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
Short summary
Short summary
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.
Tim Fischer, Annette Kock, Damian L. Arévalo-Martínez, Marcus Dengler, Peter Brandt, and Hermann W. Bange
Biogeosciences, 16, 2307–2328, https://doi.org/10.5194/bg-16-2307-2019, https://doi.org/10.5194/bg-16-2307-2019, 2019
Short summary
Short summary
We investigated air–sea gas exchange in oceanic upwelling regions for the case of nitrous oxide off Peru. In this region, routine concentration measurements from ships at 5 m or 10 m depth prove to overestimate surface (bulk) concentration. Thus, standard estimates of gas exchange will show systematic error. This is due to very shallow stratified layers that inhibit exchange between surface water and waters below and can exist for several days. Maximum bias occurs in moderate wind conditions.
Qixing Ji, Mark A. Altabet, Hermann W. Bange, Michelle I. Graco, Xiao Ma, Damian L. Arévalo-Martínez, and Damian S. Grundle
Biogeosciences, 16, 2079–2093, https://doi.org/10.5194/bg-16-2079-2019, https://doi.org/10.5194/bg-16-2079-2019, 2019
Short summary
Short summary
A strong El Niño event occurred in the Peruvian coastal region in 2015–2016, during which higher sea surface temperatures co-occurred with significantly lower sea-to-air fluxes of nitrous oxide, an important greenhouse gas and ozone depletion agent. Stratified water column during El Niño retained a larger amount of nitrous oxide that was produced via multiple microbial pathways; and intense nitrous oxide effluxes could occur when normal upwelling is resumed after El Niño.
Alexander Zavarsky and Christa A. Marandino
Atmos. Chem. Phys., 19, 1819–1834, https://doi.org/10.5194/acp-19-1819-2019, https://doi.org/10.5194/acp-19-1819-2019, 2019
Short summary
Short summary
Wind–wave interaction can suppress gas transfer between the atmosphere and the ocean. Using a global wave model we investigate the impact of this interaction on the global gas transfer of CO2 and DMS. We also investigate the impact on of gas transfer limitation on two commonly used gas transfer velocity parameterizations.
Samuel T. Wilson, Hermann W. Bange, Damian L. Arévalo-Martínez, Jonathan Barnes, Alberto V. Borges, Ian Brown, John L. Bullister, Macarena Burgos, David W. Capelle, Michael Casso, Mercedes de la Paz, Laura Farías, Lindsay Fenwick, Sara Ferrón, Gerardo Garcia, Michael Glockzin, David M. Karl, Annette Kock, Sarah Laperriere, Cliff S. Law, Cara C. Manning, Andrew Marriner, Jukka-Pekka Myllykangas, John W. Pohlman, Andrew P. Rees, Alyson E. Santoro, Philippe D. Tortell, Robert C. Upstill-Goddard, David P. Wisegarver, Gui-Ling Zhang, and Gregor Rehder
Biogeosciences, 15, 5891–5907, https://doi.org/10.5194/bg-15-5891-2018, https://doi.org/10.5194/bg-15-5891-2018, 2018
Short summary
Short summary
To determine the variability between independent measurements of dissolved methane and nitrous oxide, seawater samples were analyzed by multiple laboratories. The results revealed the influences of the different parts of the analytical process, from the initial sample collection to the calculation of the final concentrations. Recommendations are made to improve dissolved methane and nitrous oxide measurements to help preclude future analytical discrepancies between laboratories.
Robyn Butler, Paul I. Palmer, Liang Feng, Stephen J. Andrews, Elliot L. Atlas, Lucy J. Carpenter, Valeria Donets, Neil R. P. Harris, Stephen A. Montzka, Laura L. Pan, Ross J. Salawitch, and Sue M. Schauffler
Atmos. Chem. Phys., 18, 13135–13153, https://doi.org/10.5194/acp-18-13135-2018, https://doi.org/10.5194/acp-18-13135-2018, 2018
Short summary
Short summary
Natural sources of short-lived bromoform and dibromomethane are important for determining the inorganic bromine budget in the stratosphere that drives ozone loss. Two new modelling techniques describe how different geographical source regions influence their atmospheric variability over the western Pacific. We find that it is driven primarily by open ocean sources, and we use atmospheric observations to help estimate their contributions to the upper tropospheric inorganic bromine budget.
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
Short summary
Short summary
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.
Amanda C. Maycock, Katja Matthes, Susann Tegtmeier, Hauke Schmidt, Rémi Thiéblemont, Lon Hood, Hideharu Akiyoshi, Slimane Bekki, Makoto Deushi, Patrick Jöckel, Oliver Kirner, Markus Kunze, Marion Marchand, Daniel R. Marsh, Martine Michou, David Plummer, Laura E. Revell, Eugene Rozanov, Andrea Stenke, Yousuke Yamashita, and Kohei Yoshida
Atmos. Chem. Phys., 18, 11323–11343, https://doi.org/10.5194/acp-18-11323-2018, https://doi.org/10.5194/acp-18-11323-2018, 2018
Short summary
Short summary
The 11-year solar cycle is an important driver of climate variability. Changes in incoming solar ultraviolet radiation affect atmospheric ozone, which in turn influences atmospheric temperatures. Constraining the impact of the solar cycle on ozone is therefore important for understanding climate variability. This study examines the representation of the solar influence on ozone in numerical models used to simulate past and future climate. We highlight important differences among model datasets.
Richard Newton, Geraint Vaughan, Eric Hintsa, Michal T. Filus, Laura L. Pan, Shawn Honomichl, Elliot Atlas, Stephen J. Andrews, and Lucy J. Carpenter
Atmos. Chem. Phys., 18, 5157–5171, https://doi.org/10.5194/acp-18-5157-2018, https://doi.org/10.5194/acp-18-5157-2018, 2018
Short summary
Short summary
We consider the ozone measurements from aircraft during the CAST/CONTRAST/ATTREX campaigns of 2014. Low concentrations of ozone were found in the layer of 10–15 km altitude, which is indicative of uplift of ozone-poor air from near the sea surface to 10–15 km altitude. Chemicals that have origins in the sea were found in greater abundance when ozone concentrations were low compared to when ozone concentrations were high. The lowest ozone concentrations were found in the Southern Hemisphere.
Dennis Booge, Cathleen Schlundt, Astrid Bracher, Sonja Endres, Birthe Zäncker, and Christa A. Marandino
Biogeosciences, 15, 649–667, https://doi.org/10.5194/bg-15-649-2018, https://doi.org/10.5194/bg-15-649-2018, 2018
Short summary
Short summary
Our isoprene data from field measurements in the mixed layer from the Indian Ocean and the eastern Pacific Ocean show that the ability of different phytoplankton functional types to produce isoprene seems to be mainly influenced by light, ocean temperature, salinity, and nutrients. By calculating in-field isoprene production rates, we demonstrate that an additional loss is needed to explain the measured isoprene concentration, which is potentially due to degradation or consumption by bacteria.
Johanna Maltby, Lea Steinle, Carolin R. Löscher, Hermann W. Bange, Martin A. Fischer, Mark Schmidt, and Tina Treude
Biogeosciences, 15, 137–157, https://doi.org/10.5194/bg-15-137-2018, https://doi.org/10.5194/bg-15-137-2018, 2018
Short summary
Short summary
The activity and environmental controls of methanogenesis (MG) within the sulfate-reducing zone (0–30 cm below the seafloor) were investigated in organic-rich sediments of the seasonally hypoxic Eckernförde Bay, SW Baltic Sea. MG activity was mostly linked to non-competitive substrates. The major controls identified were organic matter availability, C / N, temperature, and O2 in the water column, revealing higher rates in warm, stratified, hypoxic seasons compared to colder, oxygenated seasons.
Theodore K. Koenig, Rainer Volkamer, Sunil Baidar, Barbara Dix, Siyuan Wang, Daniel C. Anderson, Ross J. Salawitch, Pamela A. Wales, Carlos A. Cuevas, Rafael P. Fernandez, Alfonso Saiz-Lopez, Mathew J. Evans, Tomás Sherwen, Daniel J. Jacob, Johan Schmidt, Douglas Kinnison, Jean-François Lamarque, Eric C. Apel, James C. Bresch, Teresa Campos, Frank M. Flocke, Samuel R. Hall, Shawn B. Honomichl, Rebecca Hornbrook, Jørgen B. Jensen, Richard Lueb, Denise D. Montzka, Laura L. Pan, J. Michael Reeves, Sue M. Schauffler, Kirk Ullmann, Andrew J. Weinheimer, Elliot L. Atlas, Valeria Donets, Maria A. Navarro, Daniel Riemer, Nicola J. Blake, Dexian Chen, L. Gregory Huey, David J. Tanner, Thomas F. Hanisco, and Glenn M. Wolfe
Atmos. Chem. Phys., 17, 15245–15270, https://doi.org/10.5194/acp-17-15245-2017, https://doi.org/10.5194/acp-17-15245-2017, 2017
Short summary
Short summary
Tropospheric inorganic bromine (BrO and Bry) shows a C-shaped profile over the tropical western Pacific Ocean, and supports previous speculation that marine convection is a source for inorganic bromine from sea salt to the upper troposphere. The Bry profile in the tropical tropopause layer (TTL) is complex, suggesting that the total Bry budget in the TTL is not closed without considering aerosol bromide. The implications for atmospheric composition and bromine sources are discussed.
Sean M. Davis, Michaela I. Hegglin, Masatomo Fujiwara, Rossana Dragani, Yayoi Harada, Chiaki Kobayashi, Craig Long, Gloria L. Manney, Eric R. Nash, Gerald L. Potter, Susann Tegtmeier, Tao Wang, Krzysztof Wargan, and Jonathon S. Wright
Atmos. Chem. Phys., 17, 12743–12778, https://doi.org/10.5194/acp-17-12743-2017, https://doi.org/10.5194/acp-17-12743-2017, 2017
Short summary
Short summary
Ozone and water vapor in the stratosphere are important gases that affect surface climate and absorb incoming solar ultraviolet radiation. These gases are represented in reanalyses, which create a complete picture of the state of Earth's atmosphere using limited observations. We evaluate reanalysis water vapor and ozone fidelity by intercomparing them, and comparing them to independent observations. Generally reanalyses do a good job at representing ozone, but have problems with water vapor.
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
Short summary
Short summary
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.
Chun-Ying Liu, Wei-Hua Feng, Ye Tian, Gui-Peng Yang, Pei-Feng Li, and Hermann W. Bange
Ocean Sci., 13, 623–632, https://doi.org/10.5194/os-13-623-2017, https://doi.org/10.5194/os-13-623-2017, 2017
Short summary
Short summary
We developed a new method for the determination of dissolved nitric oxide (NO) in discrete seawater samples based on the combination of a purge-and-trap setup and a fluorometric detection of NO. With this method we have a reliable and comparably easy to use method to measure oceanic NO surface concentrations, which can be used to decipher both its temporal and spatial distributions as well as its biogeochemical pathways in the oceans.
Maria A. Navarro, Alfonso Saiz-Lopez, Carlos A. Cuevas, Rafael P. Fernandez, Elliot Atlas, Xavier Rodriguez-Lloveras, Douglas Kinnison, Jean-Francois Lamarque, Simone Tilmes, Troy Thornberry, Andrew Rollins, James W. Elkins, Eric J. Hintsa, and Fred L. Moore
Atmos. Chem. Phys., 17, 9917–9930, https://doi.org/10.5194/acp-17-9917-2017, https://doi.org/10.5194/acp-17-9917-2017, 2017
Short summary
Short summary
Inorganic bromine (Bry) plays an important role in ozone layer depletion. Based on aircraft observations of organic bromine species and chemistry simulations, we model the Bry abundances over the Pacific tropical tropopause. Our results show BrO and Br as the dominant species during daytime hours, and BrCl and BrONO2 as the nighttime dominant species over the western and eastern Pacific, respectively. The difference in the partitioning is due to changes in the abundance of O3, NO2, and Cly.
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
Short summary
Short summary
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.
Lea Steinle, Johanna Maltby, Tina Treude, Annette Kock, Hermann W. Bange, Nadine Engbersen, Jakob Zopfi, Moritz F. Lehmann, and Helge Niemann
Biogeosciences, 14, 1631–1645, https://doi.org/10.5194/bg-14-1631-2017, https://doi.org/10.5194/bg-14-1631-2017, 2017
Short summary
Short summary
Large amounts of methane are produced in anoxic, coastal sediments, from which it can seep into the overlying water column. Aerobic oxidation of methane (MOx) mediated by methanotrophic bacteria is an important sink for methane before its evasion to the atmosphere. In a 2-year seasonal study, we investigated the spatio-temporal variability of MOx in a seasonally hypoxic coastal inlet using radiotracer-based methods. In experiments, we assessed the effect of variable oxygen concentrations on MOx.
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
Short summary
Short summary
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
Short summary
Short summary
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.
Brian M. Lerner, Jessica B. Gilman, Kenneth C. Aikin, Elliot L. Atlas, Paul D. Goldan, Martin Graus, Roger Hendershot, Gabriel A. Isaacman-VanWertz, Abigail Koss, William C. Kuster, Richard A. Lueb, Richard J. McLaughlin, Jeff Peischl, Donna Sueper, Thomas B. Ryerson, Travis W. Tokarek, Carsten Warneke, Bin Yuan, and Joost A. de Gouw
Atmos. Meas. Tech., 10, 291–313, https://doi.org/10.5194/amt-10-291-2017, https://doi.org/10.5194/amt-10-291-2017, 2017
Short summary
Short summary
Whole air sampling followed by analysis by gas chromatography is a common technique for characterization of trace volatile organic compounds in the atmosphere. We describe a new automated gas chromatograph–mass spectrograph which uses a Stirling cooler for sample preconcentration at −165 °C without the need for a cryogen such as liquid nitrogen. We also discuss potential sources of artifacts from our electropolished stainless steel sampling system and present results from two field campaigns.
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
Short summary
Short summary
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
Short summary
Short summary
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.
Martyn P. Chipperfield, Qing Liang, Matthew Rigby, Ryan Hossaini, Stephen A. Montzka, Sandip Dhomse, Wuhu Feng, Ronald G. Prinn, Ray F. Weiss, Christina M. Harth, Peter K. Salameh, Jens Mühle, Simon O'Doherty, Dickon Young, Peter G. Simmonds, Paul B. Krummel, Paul J. Fraser, L. Paul Steele, James D. Happell, Robert C. Rhew, James Butler, Shari A. Yvon-Lewis, Bradley Hall, David Nance, Fred Moore, Ben R. Miller, James W. Elkins, Jeremy J. Harrison, Chris D. Boone, Elliot L. Atlas, and Emmanuel Mahieu
Atmos. Chem. Phys., 16, 15741–15754, https://doi.org/10.5194/acp-16-15741-2016, https://doi.org/10.5194/acp-16-15741-2016, 2016
Short summary
Short summary
Carbon tetrachloride (CCl4) is a compound which, when released into the atmosphere, can cause depletion of the stratospheric ozone layer. Its emissions are controlled under the Montreal Protocol, and its atmospheric abundance is slowly decreasing. However, this decrease is not as fast as expected based on estimates of its emissions and its atmospheric lifetime. We have used an atmospheric model to look at the uncertainties in the CCl4 lifetime and to examine the impact on its atmospheric decay.
Stephen J. Andrews, Lucy J. Carpenter, Eric C. Apel, Elliot Atlas, Valeria Donets, James R. Hopkins, Rebecca S. Hornbrook, Alastair C. Lewis, Richard T. Lidster, Richard Lueb, Jamie Minaeian, Maria Navarro, Shalini Punjabi, Daniel Riemer, and Sue Schauffler
Atmos. Meas. Tech., 9, 5213–5225, https://doi.org/10.5194/amt-9-5213-2016, https://doi.org/10.5194/amt-9-5213-2016, 2016
Short summary
Short summary
We present a comparison of aircraft measurements of important trace gases from a co-ordinated campaign in Jan–Feb 2014 in the tropical west Pacific involving the NASA Global Hawk, NCAR GV and FAAM BAe-146 aircraft.
The paper studies the comparability of separate measurements across platforms and demonstrates that aircraft measurements are relevant for characterising the vertical uplift of important gases, such as those with ozone-depleting potential, to the upper troposphere–lower stratosphere.
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
Short summary
Short summary
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
Short summary
Short summary
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.
Dennis Booge, Christa A. Marandino, Cathleen Schlundt, Paul I. Palmer, Michael Schlundt, Elliot L. Atlas, Astrid Bracher, Eric S. Saltzman, and Douglas W. R. Wallace
Atmos. Chem. Phys., 16, 11807–11821, https://doi.org/10.5194/acp-16-11807-2016, https://doi.org/10.5194/acp-16-11807-2016, 2016
Short summary
Short summary
Isoprene, a biogenic trace gas, is an important precursor of secondary organic aerosol/cloud condensation nuclei. Here, we use isoprene and related field measurements from three different ocean data sets together with remotely sensed satellite data to model global marine isoprene emissions. Our findings suggest that there is at least one missing oceanic source of isoprene and possibly other unknown factors in the ocean or atmosphere influencing the atmospheric values.
Amanda C. Maycock, Katja Matthes, Susann Tegtmeier, Rémi Thiéblemont, and Lon Hood
Atmos. Chem. Phys., 16, 10021–10043, https://doi.org/10.5194/acp-16-10021-2016, https://doi.org/10.5194/acp-16-10021-2016, 2016
Short summary
Short summary
The impact of changes in incoming solar radiation on stratospheric ozone has important impacts on the atmosphere. Understanding this ozone response is crucial for constraining how solar activity affects climate. This study analyses the solar ozone response (SOR) in satellite datasets and shows that there are substantial differences in the magnitude and spatial structure across different records. In particular, the SOR in the new SAGE v7.0 mixing ratio data is smaller than in the previous v6.2.
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
Lothar Stramma, Tim Fischer, Damian S. Grundle, Gerd Krahmann, Hermann W. Bange, and Christa A. Marandino
Ocean Sci., 12, 861–873, https://doi.org/10.5194/os-12-861-2016, https://doi.org/10.5194/os-12-861-2016, 2016
Short summary
Short summary
Results from a research cruise on R/V Sonne to the eastern tropical Pacific in October 2015 during the 2015–2016 El Niño show the transition of current, hydrographic, and nutrient conditions to El Niño conditions in the eastern tropical Pacific in October 2015. Although in early 2015 the El Niño was strong and in October 2015 showed a clear El Niño influence on the EUC, in the eastern tropical Pacific the measurements only showed developing El Niño water mass distributions.
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
Short summary
Short summary
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.
Carolin R. Löscher, Hermann W. Bange, Ruth A. Schmitz, Cameron M. Callbeck, Anja Engel, Helena Hauss, Torsten Kanzow, Rainer Kiko, Gaute Lavik, Alexandra Loginova, Frank Melzner, Judith Meyer, Sven C. Neulinger, Markus Pahlow, Ulf Riebesell, Harald Schunck, Sören Thomsen, and Hannes Wagner
Biogeosciences, 13, 3585–3606, https://doi.org/10.5194/bg-13-3585-2016, https://doi.org/10.5194/bg-13-3585-2016, 2016
Short summary
Short summary
The ocean loses oxygen due to climate change. Addressing this issue in tropical ocean regions (off Peru and Mauritania), we aimed to understand the effects of oxygen depletion on various aspects of marine biogeochemistry, including primary production and export production, the nitrogen cycle, greenhouse gas production, organic matter fluxes and remineralization, and the role of zooplankton and viruses.
Carolin R. Löscher, Annie Bourbonnais, Julien Dekaezemacker, Chawalit N. Charoenpong, Mark A. Altabet, Hermann W. Bange, Rena Czeschel, Chris Hoffmann, and Ruth Schmitz
Biogeosciences, 13, 2889–2899, https://doi.org/10.5194/bg-13-2889-2016, https://doi.org/10.5194/bg-13-2889-2016, 2016
Short summary
Short summary
The ocean is full of eddies and they play a key role for ocean biogeochemistry. In order to understand dinitrogen (N2) fixation, one major control of oceanic primary production, we investigated three eddies in the eastern tropical South Pacific off Peru. We conducted the first detailed survey and found increased N2 fixation in the oxygen-depleted cores of anticyclonic mode water eddies. Taken together, we could – for the first time – show that eddies play an important role in N2 fixation off Peru.
Denise Müller, Hermann W. Bange, Thorsten Warneke, Tim Rixen, Moritz Müller, Aazani Mujahid, and Justus Notholt
Biogeosciences, 13, 2415–2428, https://doi.org/10.5194/bg-13-2415-2016, https://doi.org/10.5194/bg-13-2415-2016, 2016
Short summary
Short summary
Estuaries act as sources of the greenhouse gases nitrous oxide (N2O) and methane (CH4) to the atmosphere. We provide first measurements of N2O and CH4 in two estuaries in north-western Borneo, a region which is dominated by peatlands. We show that N2O and CH4 concentrations in these estuaries are moderate despite high organic carbon loads, that nutrient enhancement does not lead to enhanced N2O emissions, and that the wet season dominates the variability of the emissions in these systems.
Happy Hu, Annie Bourbonnais, Jennifer Larkum, Hermann W. Bange, and Mark A. Altabet
Biogeosciences, 13, 1453–1468, https://doi.org/10.5194/bg-13-1453-2016, https://doi.org/10.5194/bg-13-1453-2016, 2016
Damian L. Arévalo-Martínez, Annette Kock, Carolin R. Löscher, Ruth A. Schmitz, Lothar Stramma, and Hermann W. Bange
Biogeosciences, 13, 1105–1118, https://doi.org/10.5194/bg-13-1105-2016, https://doi.org/10.5194/bg-13-1105-2016, 2016
Short summary
Short summary
We present the first measurements of N2O across three mesoscale eddies in the eastern tropical South Pacific. Eddie's vertical structure, offshore transport, properties during its formation and near-surface primary production determined the N2O distribution. Substantial depletion of N2O within the core of anticyclonic eddies suggests that although these are transient features, N-loss processes within their centres can lead to an enhanced N2O sink which is not accounted for in marine N2O budgets.
A. Kock, D. L. Arévalo-Martínez, C. R. Löscher, and H. W. Bange
Biogeosciences, 13, 827–840, https://doi.org/10.5194/bg-13-827-2016, https://doi.org/10.5194/bg-13-827-2016, 2016
Short summary
Short summary
We measured the nitrous oxide (N2O) distribution in the water column in the oxygen minimum zone off Peru, an area with extremely high N2O emissions. Our data show very variable and often very high N2O concentrations in the water column at the coast, which lead to high N2O emissions when these waters are brought to the surface. The very high N2O production off Peru may be caused by high nutrient turnover rates together with rapid changes in the oxygen concentrations.
A. R. Baker, M. Thomas, H. W. Bange, and E. Plasencia Sánchez
Biogeosciences, 13, 817–825, https://doi.org/10.5194/bg-13-817-2016, https://doi.org/10.5194/bg-13-817-2016, 2016
Short summary
Short summary
Concentrations of major ions and trace metals were measured in aerosols off the coast of Peru in December 2012. A few trace metals (iron, copper, nickel, and cobalt) had anomalously high concentrations, which may be associated with industrial metal smelting activities in the region. The atmosphere appears to supply an excess of iron (relative to atmospheric nitrogen supply) to the phytoplankton community of the Peruvian upwelling system.
S. Tegtmeier, M. I. Hegglin, J. Anderson, B. Funke, J. Gille, A. Jones, L. Smith, T. von Clarmann, and K. A. Walker
Earth Syst. Sci. Data, 8, 61–78, https://doi.org/10.5194/essd-8-61-2016, https://doi.org/10.5194/essd-8-61-2016, 2016
Short summary
Short summary
The first comprehensive intercomparison of CFC-11, CFC-12, HF, and SF6 satellite data was performed as part of the SPARC Data Initiative following a new "top-down" concept of satellite measurement validation and thus providing a global picture of the data characteristics. The comparisons will provide basic information on quality and consistency of the various data sets and will serve as a guide for their use in empirical studies of climate and variability, and in model-measurement comparisons.
D. Müller, T. Warneke, T. Rixen, M. Müller, A. Mujahid, H. W. Bange, and J. Notholt
Biogeosciences, 13, 691–705, https://doi.org/10.5194/bg-13-691-2016, https://doi.org/10.5194/bg-13-691-2016, 2016
Short summary
Short summary
We studied organic carbon and the dissolved greenhouse gases carbon dioxide (CO2) and carbon monoxide (CO) in two estuaries in Sarawak, Malaysia, whose coast is covered by carbon-rich peatlands. The estuaries received terrestrial organic carbon from peat-draining tributaries. A large fraction was converted to CO2 and a minor fraction to CO. Both gases were released to the atmosphere. This shows how these estuaries function as efficient filters between land and ocean in this important region.
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
Short summary
Short summary
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. E. Lutterbeck and H. W. Bange
Ocean Sci., 11, 937–946, https://doi.org/10.5194/os-11-937-2015, https://doi.org/10.5194/os-11-937-2015, 2015
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
Short summary
Short summary
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
Short summary
Short summary
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.
Fuqing Zhang, Junhong Wei, Meng Zhang, K. P. Bowman, L. L. Pan, E. Atlas, and S. C. Wofsy
Atmos. Chem. Phys., 15, 7667–7684, https://doi.org/10.5194/acp-15-7667-2015, https://doi.org/10.5194/acp-15-7667-2015, 2015
Short summary
Short summary
Based on spectral and wavelet analyses, along with a diagnosis of the polarization relations, this study analyzes in situ airborne measurements from the 2008 Stratosphere-Troposphere Analyses of Regional Transport (START08) experiment to characterize gravity waves in the extratropical upper troposphere and lower stratosphere (ExUTLS) region. The focus is on the second research flight (RF02), which was dedicated to probing gravity waves associated with strong upper-tropospheric jet-front systems.
S. Tilmes, J.-F. Lamarque, L. K. Emmons, D. E. Kinnison, P.-L. Ma, X. Liu, S. Ghan, C. Bardeen, S. Arnold, M. Deeter, F. Vitt, T. Ryerson, J. W. Elkins, F. Moore, J. R. Spackman, and M. Val Martin
Geosci. Model Dev., 8, 1395–1426, https://doi.org/10.5194/gmd-8-1395-2015, https://doi.org/10.5194/gmd-8-1395-2015, 2015
Short summary
Short summary
The Community Atmosphere Model (CAM), version 5, is now coupled to extensive tropospheric and stratospheric chemistry, called CAM5-chem, and is available in addition to CAM4-chem in the Community Earth System Model (CESM) version 1.2. Both configurations are well suited as tools for atmospheric chemistry modeling studies in the troposphere and lower stratosphere.
T. G. Bell, W. De Bruyn, C. A. Marandino, S. D. Miller, C. S. Law, M. J. Smith, and E. S. Saltzman
Atmos. Chem. Phys., 15, 1783–1794, https://doi.org/10.5194/acp-15-1783-2015, https://doi.org/10.5194/acp-15-1783-2015, 2015
P. Brandt, H. W. Bange, D. Banyte, M. Dengler, S.-H. Didwischus, T. Fischer, R. J. Greatbatch, J. Hahn, T. Kanzow, J. Karstensen, A. Körtzinger, G. Krahmann, S. Schmidtko, L. Stramma, T. Tanhua, and M. Visbeck
Biogeosciences, 12, 489–512, https://doi.org/10.5194/bg-12-489-2015, https://doi.org/10.5194/bg-12-489-2015, 2015
Short summary
Short summary
Our observational study looks at the structure of the eastern tropical North Atlantic (ETNA) oxygen minimum zone (OMZ) in comparison with the less-ventilated, eastern tropical South Pacific OMZ. We quantify the OMZ’s oxygen budget composed of consumption, advection, lateral and vertical mixing. Substantial oxygen variability is observed on interannual to multidecadal timescales. The deoxygenation of the ETNA OMZ during the last decades represents a substantial imbalance of the oxygen budget.
M. Toohey, K. Krüger, M. Bittner, C. Timmreck, and H. Schmidt
Atmos. Chem. Phys., 14, 13063–13079, https://doi.org/10.5194/acp-14-13063-2014, https://doi.org/10.5194/acp-14-13063-2014, 2014
Short summary
Short summary
Earth system model simulations are used to investigate the impact of volcanic aerosol forcing on stratospheric dynamics, e.g. the Northern Hemisphere (NH) polar vortex. We find that mechanisms linking aerosol heating and high-latitude dynamics are not as direct as often assumed; high-latitude effects result from changes in stratospheric circulation and related vertical motions. The simulated responses also show evidence of being sensitive to the structure of the volcanic forcing used.
S. T. Lennartz, A. Lehmann, J. Herrford, F. Malien, H.-P. Hansen, H. Biester, and H. W. Bange
Biogeosciences, 11, 6323–6339, https://doi.org/10.5194/bg-11-6323-2014, https://doi.org/10.5194/bg-11-6323-2014, 2014
Short summary
Short summary
A time series of nine oceanic parameters from the coastal time series station Boknis Eck (BE, southwestern Baltic Sea) in the period of 1957-2013 is analysed with respect to seasonal cycles and long-term trends. Most striking was a paradoxical decreasing trend in oxygen with a simultaneous decline in eutrophication. Possible reasons for this paradox, e.g. processes related to warming temperatures such as increased decomposition of organic matter or altered ventilation, are discussed.
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
G. W. Santoni, B. C. Daube, E. A. Kort, R. Jiménez, S. Park, J. V. Pittman, E. Gottlieb, B. Xiang, M. S. Zahniser, D. D. Nelson, J. B. McManus, J. Peischl, T. B. Ryerson, J. S. Holloway, A. E. Andrews, C. Sweeney, B. Hall, E. J. Hintsa, F. L. Moore, J. W. Elkins, D. F. Hurst, B. B. Stephens, J. Bent, and S. C. Wofsy
Atmos. Meas. Tech., 7, 1509–1526, https://doi.org/10.5194/amt-7-1509-2014, https://doi.org/10.5194/amt-7-1509-2014, 2014
D. R. Gentner, T. B. Ford, A. Guha, K. Boulanger, J. Brioude, W. M. Angevine, J. A. de Gouw, C. Warneke, J. B. Gilman, T. B. Ryerson, J. Peischl, S. Meinardi, D. R. Blake, E. Atlas, W. A. Lonneman, T. E. Kleindienst, M. R. Beaver, J. M. St. Clair, P. O. Wennberg, T. C. VandenBoer, M. Z. Markovic, J. G. Murphy, R. A. Harley, and A. H. Goldstein
Atmos. Chem. Phys., 14, 4955–4978, https://doi.org/10.5194/acp-14-4955-2014, https://doi.org/10.5194/acp-14-4955-2014, 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
C. J. Young, R. A. Washenfelder, P. M. Edwards, D. D. Parrish, J. B. Gilman, W. C. Kuster, L. H. Mielke, H. D. Osthoff, C. Tsai, O. Pikelnaya, J. Stutz, P. R. Veres, J. M. Roberts, S. Griffith, S. Dusanter, P. S. Stevens, J. Flynn, N. Grossberg, B. Lefer, J. S. Holloway, J. Peischl, T. B. Ryerson, E. L. Atlas, D. R. Blake, and S. S. Brown
Atmos. Chem. Phys., 14, 3427–3440, https://doi.org/10.5194/acp-14-3427-2014, https://doi.org/10.5194/acp-14-3427-2014, 2014
J. Friedrich, F. Janssen, D. Aleynik, H. W. Bange, N. Boltacheva, M. N. Çagatay, A. W. Dale, G. Etiope, Z. Erdem, M. Geraga, A. Gilli, M. T. Gomoiu, P. O. J. Hall, D. Hansson, Y. He, M. Holtappels, M. K. Kirf, M. Kononets, S. Konovalov, A. Lichtschlag, D. M. Livingstone, G. Marinaro, S. Mazlumyan, S. Naeher, R. P. North, G. Papatheodorou, O. Pfannkuche, R. Prien, G. Rehder, C. J. Schubert, T. Soltwedel, S. Sommer, H. Stahl, E. V. Stanev, A. Teaca, A. Tengberg, C. Waldmann, B. Wehrli, and F. Wenzhöfer
Biogeosciences, 11, 1215–1259, https://doi.org/10.5194/bg-11-1215-2014, https://doi.org/10.5194/bg-11-1215-2014, 2014
B. D. Hall, A. Engel, J. Mühle, J. W. Elkins, F. Artuso, E. Atlas, M. Aydin, D. Blake, E.-G. Brunke, S. Chiavarini, P. J. Fraser, J. Happell, P. B. Krummel, I. Levin, M. Loewenstein, M. Maione, S. A. Montzka, S. O'Doherty, S. Reimann, G. Rhoderick, E. S. Saltzman, H. E. Scheel, L. P. Steele, M. K. Vollmer, R. F. Weiss, D. Worthy, and Y. Yokouchi
Atmos. Meas. Tech., 7, 469–490, https://doi.org/10.5194/amt-7-469-2014, https://doi.org/10.5194/amt-7-469-2014, 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. L. Arévalo-Martínez, M. Beyer, M. Krumbholz, I. Piller, A. Kock, T. Steinhoff, A. Körtzinger, and H. W. Bange
Ocean Sci., 9, 1071–1087, https://doi.org/10.5194/os-9-1071-2013, https://doi.org/10.5194/os-9-1071-2013, 2013
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
S. S. Brown, W. P. Dubé, R. Bahreini, A. M. Middlebrook, C. A. Brock, C. Warneke, J. A. de Gouw, R. A. Washenfelder, E. Atlas, J. Peischl, T. B. Ryerson, J. S. Holloway, J. P. Schwarz, R. Spackman, M. Trainer, D. D. Parrish, F. C. Fehshenfeld, and A. R. Ravishankara
Atmos. Chem. Phys., 13, 11317–11337, https://doi.org/10.5194/acp-13-11317-2013, https://doi.org/10.5194/acp-13-11317-2013, 2013
L. Stramma, H. W. Bange, R. Czeschel, A. Lorenzo, and M. Frank
Biogeosciences, 10, 7293–7306, https://doi.org/10.5194/bg-10-7293-2013, https://doi.org/10.5194/bg-10-7293-2013, 2013
I.-N. Kim, K. Lee, H. W. Bange, and A. M. Macdonald
Biogeosciences, 10, 6783–6792, https://doi.org/10.5194/bg-10-6783-2013, https://doi.org/10.5194/bg-10-6783-2013, 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
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, Emma C. Leedham Elvidge, 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
K. Laß, H. W. Bange, and G. Friedrichs
Biogeosciences, 10, 5325–5334, https://doi.org/10.5194/bg-10-5325-2013, https://doi.org/10.5194/bg-10-5325-2013, 2013
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
C. Zindler, A. Bracher, C. A. Marandino, B. Taylor, E. Torrecilla, A. Kock, and H. W. Bange
Biogeosciences, 10, 3297–3311, https://doi.org/10.5194/bg-10-3297-2013, https://doi.org/10.5194/bg-10-3297-2013, 2013
K. Großmann, U. Frieß, E. Peters, F. Wittrock, J. Lampel, S. Yilmaz, J. Tschritter, R. Sommariva, R. von Glasow, B. Quack, K. Krüger, K. Pfeilsticker, and U. Platt
Atmos. Chem. Phys., 13, 3363–3378, https://doi.org/10.5194/acp-13-3363-2013, https://doi.org/10.5194/acp-13-3363-2013, 2013
L. M. Zamora, A. Oschlies, H. W. Bange, K. B. Huebert, J. D. Craig, A. Kock, and C. R. Löscher
Biogeosciences, 9, 5007–5022, https://doi.org/10.5194/bg-9-5007-2012, https://doi.org/10.5194/bg-9-5007-2012, 2012
Related subject area
Subject: Gases | Research Activity: Field Measurements | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Marine emissions and trade winds control the atmospheric nitrous oxide in the Galapagos Islands
Measurement report: A complex street-level air quality observation campaign in a heavy-traffic area utilizing the multivariate adaptive regression splines method for field calibration of low-cost sensors
The impact of organic nitrates on summer ozone formation in Shanghai, China
Differences in the key volatile organic compound species between their emitted and ambient concentrations in ozone formation
Mechanistic insights into chloroacetic acid production from atmospheric multiphase volatile organic compound–chlorine chemistry
Accurate elucidation of oxidation under heavy ozone pollution: a full suite of radical measurements in the chemically complex atmosphere
Carbonyl compounds from typical combustion sources: emission characteristics, influencing factors, and their contribution to ozone formation
Emissions of intermediate-volatility and semi-volatile organic compounds (I/SVOCs) from different cumulative-mileage diesel vehicles at various ambient temperatures
Characterization of nitrous acid and its potential effects on secondary pollution in the warm season in Beijing urban areas
Vertical changes in volatile organic compounds (VOCs) and impacts on photochemical ozone formation
Diurnal, seasonal, and interannual variations in δ(18O) of atmospheric O2 and its application to evaluate natural and anthropogenic changes in oxygen, carbon, and water cycles
Cloud processing of dimethyl sulfide (DMS) oxidation products limits sulfur dioxide (SO2) and carbonyl sulfide (OCS) production in the eastern North Atlantic marine boundary layer
Atmospheric carbonyl compounds are crucial in regional ozone heavy pollution: insights from the Chengdu Plain Urban Agglomeration, China
Understanding summertime peroxyacetyl nitrate (PAN) formation and its relation to aerosol pollution: insights from high-resolution measurements and modeling
Measurement report: Exploring the variations in ambient BTEX in urban Europe and their environmental health implications
Seasonal air concentration variability, gas–particle partitioning, precipitation scavenging, and air–water equilibrium of organophosphate esters in southern Canada
Global Ground-based Tropospheric Ozone Measurements: Reference Data and Individual Site Trends (2000–2022) from the TOAR-II/HEGIFTOM Project
Measurement report: Surface exchange fluxes of HONO during the growth process of paddy fields in the Huaihe River Basin, China
Molecular and seasonal characteristics of organic vapors in urban Beijing: insights from Vocus-PTR measurements
The variations in volatile organic compounds based on the policy change for Omicron in the traffic hub of Zhengzhou
On the dynamics of ozone depletion events at Villum Research Station in the High Arctic
VOC sources and impacts at an urban Mediterranean area (Marseille – France)
Measurement report: Long-term measurements of surface ozone and trends in semi-natural sub-Saharan African ecosystems
Characterization of biogenic volatile organic compounds and their oxidation products in a stressed spruce-dominated forest close to a biogas power plant
Reactive chlorine-, sulfur-, and nitrogen-containing volatile organic compounds impact atmospheric chemistry in the megacity of Delhi during both clean and extremely polluted seasons
Analysis of the day-to-day variability of ozone vertical profiles in the lower troposphere during the 2022 Paris ACROSS campaign
Significant influence of oxygenated volatile organic compounds on atmospheric chemistry analysis: A case study in a typical industrial city in China
Short lifetimes of organic nitrates in a sub-urban temperate forest indicate efficient assimilation of reactive nitrogen by the biosphere
Ozone deposition measurements over wheat fields in the North China Plain: variability and related factors of deposition flux and velocity
Consistency evaluation of tropospheric ozone from ozonesonde and IAGOS (In-service Aircraft for a Global Observing System) observations: vertical distribution, ozonesonde types, and station–airport distance
CO2 and CO temporal variability over Mexico City from ground-based total column and surface measurements
Investigating carbonyl compounds above the Amazon rainforest using a proton-transfer-reaction time-of-flight mass spectrometer (PTR-ToF-MS) with NO+ chemical ionization
Measurement report: In-flight and ground-based measurements of nitrogen oxide emissions from latest-generation jet engines and 100 % sustainable aviation fuel
Observation and modelling of atmospheric OH and HO2 radicals at a subtropical rural site and implications for secondary pollutants
Measurement report: Sources, sinks, and lifetime of NOx in a suburban temperate forest at night
Measurement report: Urban ammonia and amines in Houston, Texas
Biomass-burning sources control ambient particulate matter, but traffic and industrial sources control volatile organic compound (VOC) emissions and secondary-pollutant formation during extreme pollution events in Delhi
Multi-year observations of variable incomplete combustion in the New York megacity
Observations of the vertical distributions of summertime atmospheric pollutants in Nam Co: OH production and source analysis
Spatiotemporal variations in atmospheric CH4 concentrations and enhancements in northern China based on a comprehensive dataset: Ground-based observations, TROPOMI data, inventory data and inversions
Measurement report: Elevated atmospheric ammonia may promote particle pH and HONO formation – insights from the COVID-19 pandemic
Measurement report: Vertical and temporal variability in the near-surface ozone production rate and sensitivity in an urban area in the Pearl River Delta region, China
Elevated oxidized mercury in the free troposphere: analytical advances and application at a remote continental mountaintop site
Using observed urban NOx sinks to constrain VOC reactivity and the ozone and radical budget in the Seoul Metropolitan Area
Real-world emission characteristics of VOCs from typical cargo ships and their potential contributions to secondary organic aerosol and O3 under low-sulfur fuel policies
NO3 reactivity during a summer period in a temperate forest below and above the canopy
The role of oceanic ventilation and terrestrial outflow in atmospheric non-methane hydrocarbons over the Chinese marginal seas
Concentration and source changes of nitrous acid (HONO) during the COVID-19 lockdown in Beijing
Characteristics and sources of nonmethane volatile organic compounds (NMVOCs) and O3–NOx–NMVOC relationships in Zhengzhou, China
Deciphering anthropogenic and biogenic contributions to selected non-methane volatile organic compound emissions in an urban area
Timur Cinay, Dickon Young, Nazaret Narváez Jimenez, Cristina Vintimilla-Palacios, Ariel Pila Alonso, Paul B. Krummel, William Vizuete, and Andrew R. Babbin
Atmos. Chem. Phys., 25, 4703–4718, https://doi.org/10.5194/acp-25-4703-2025, https://doi.org/10.5194/acp-25-4703-2025, 2025
Short summary
Short summary
We present the initial 15 months of nitrous oxide measurements from the Galapagos Emissions Monitoring Station. The observed variability in atmospheric mole fractions during this period can be linked to several factors: seasonal variations in trade wind speed and direction across the eastern Pacific, differences in the transport history of air masses sampled, and spatiotemporal heterogeneity in regional marine nitrous oxide emissions from the coastal upwelling systems of Peru and Chile.
Petra Bauerová, Josef Keder, Adriana Šindelářová, Ondřej Vlček, William Patiño, Pavel Krč, Jan Geletič, Hynek Řezníček, Martin Bureš, Kryštof Eben, Michal Belda, Jelena Radović, Vladimír Fuka, Radek Jareš, Igor Esau, and Jaroslav Resler
Atmos. Chem. Phys., 25, 4477–4504, https://doi.org/10.5194/acp-25-4477-2025, https://doi.org/10.5194/acp-25-4477-2025, 2025
Short summary
Short summary
The study explored urban air quality in Prague using low-cost sensors and highlighted the multivariate adaptive regression splines (MARS) correction method's effectiveness in enhancing accuracy. Results showed traffic's impact on nitrogen dioxide levels and atmospheric dynamics on particulate matter. The research confirmed MARS-corrected sensors as cost-effective for monitoring, despite challenges like sensor ageing and data quality control.
Chunmeng Li, Xiaorui Chen, Haichao Wang, Tianyu Zhai, Xuefei Ma, Xinping Yang, Shiyi Chen, Min Zhou, Shengrong Lou, Xin Li, Limin Zeng, and Keding Lu
Atmos. Chem. Phys., 25, 3905–3918, https://doi.org/10.5194/acp-25-3905-2025, https://doi.org/10.5194/acp-25-3905-2025, 2025
Short summary
Short summary
This study reports an observation of organic nitrate (including total peroxy nitrates and total alkyl nitrates) in Shanghai, China, during the summer of 2021, by homemade thermal dissociation cavity-enhanced absorption spectroscopy (TD-CEAS; Atmos. Meas. Tech., 14, 4033–4051, 2021). The distribution of organic nitrates and their effects on local ozone production are analyzed based on field observations in conjunction with model simulations.
Xudong Zheng and Shaodong Xie
Atmos. Chem. Phys., 25, 3807–3820, https://doi.org/10.5194/acp-25-3807-2025, https://doi.org/10.5194/acp-25-3807-2025, 2025
Short summary
Short summary
To reduce uncertainties in identifying the key volatile organic compounds (VOCs) in ozone (O3) formation from ambient concentrations, this study comprehensively calculates the emitted VOC concentrations during both nighttime and daytime using the nitrate radical, O3, and hydroxyl radical reaction rates and ambient VOC concentrations. Based on the emitted concentrations, isoprene is one of the top three species contributing to O3 formation, which may be overlooked in observed concentrations.
Mingxue Li, Men Xia, Chunshui Lin, Yifan Jiang, Weihang Sun, Yurun Wang, Yingnan Zhang, Maoxia He, and Tao Wang
Atmos. Chem. Phys., 25, 3753–3764, https://doi.org/10.5194/acp-25-3753-2025, https://doi.org/10.5194/acp-25-3753-2025, 2025
Short summary
Short summary
Our field campaigns observed a strong diel pattern of chloroacetic acid as well as a strong correlation between its level and that of reactive chlorine species at a coastal site. Using quantum chemical calculations and box model simulation with an updated Master Chemical Mechanism, we found that the formation pathway of chloroacetic acid involved multiphase processes. Our study enhances understanding of atmospheric organic chlorine chemistry and emphasizes the importance of multiphase reactions.
Renzhi Hu, Guoxian Zhang, Haotian Cai, Jingyi Guo, Keding Lu, Xin Li, Shengrong Lou, Zhaofeng Tan, Changjin Hu, Pinhua Xie, and Wenqing Liu
Atmos. Chem. Phys., 25, 3011–3028, https://doi.org/10.5194/acp-25-3011-2025, https://doi.org/10.5194/acp-25-3011-2025, 2025
Short summary
Short summary
A full suite of radical measurements (OH, HO2, RO2, and kOH) was established to accurately elucidate the limitations of oxidation in a chemically complex atmosphere. Sensitivity tests revealed that the incorporation of complex processes enabled a balance in both radical concentrations and coordinate ratios, effectively addressing the deficiency in the ozone generation mechanism. The full-chain radical detection bridged the gap between the photochemistry and the intensive oxidation level.
Yanjie Lu, Xinxin Feng, Yanli Feng, Minjun Jiang, Yu Peng, Tian Chen, and Yingjun Chen
EGUsphere, https://doi.org/10.5194/egusphere-2025-131, https://doi.org/10.5194/egusphere-2025-131, 2025
Short summary
Short summary
The EFs of CCs from biomass burning (BB) is an order of magnitude higher than that from on-road sources. Fuel type determines the emission characteristics and composition of CCs. The formation of CCs from solid and liquid fuel sources is respectively controlled by combustion temperature and emission standards. In addition, biomass burning and agricultural machinery sources significantly contribute to the oxidizing capacity of regional atmospheres.
Shuwen Guo, Xuan Zheng, Xiao He, Lewei Zeng, Liqiang He, Xian Wu, Yifei Dai, Zihao Huang, Ting Chen, Shupei Xiao, Yan You, Sheng Xiang, Shaojun Zhang, Jingkun Jiang, and Ye Wu
Atmos. Chem. Phys., 25, 2695–2705, https://doi.org/10.5194/acp-25-2695-2025, https://doi.org/10.5194/acp-25-2695-2025, 2025
Short summary
Short summary
We considered two potential influencing factors of heavy-duty diesel vehicle emissions that are rarely mentioned in the literature: cumulative mileage and ambient temperatures. The results suggest that prolonged use of heavy-duty diesel vehicles and low ambient temperatures leads to reduced engine combustion efficiency, which in turn increases tailpipe emissions significantly.
Junling Li, Chaofan Lian, Mingyuan Liu, Hao Zhang, Yongxin Yan, Yufei Song, Chun Chen, Jiaqi Wang, Haijie Zhang, Yanqin Ren, Yucong Guo, Weigang Wang, Yisheng Xu, Hong Li, Jian Gao, and Maofa Ge
Atmos. Chem. Phys., 25, 2551–2568, https://doi.org/10.5194/acp-25-2551-2025, https://doi.org/10.5194/acp-25-2551-2025, 2025
Short summary
Short summary
As a key source of hydroxyl (OH) radical, nitrous acid (HONO) has attracted much attention for its important role in the atmospheric oxidant capacity (AOC) increase. In this study, we made a comparison of the ambient levels, variation patterns, sources, and formation pathway in the warm season on the basis of continuous intensive observations at an urban site of Beijing. This work highlights the importance of HONO for the AOC in the warm season.
Xiao-Bing Li, Bin Yuan, Yibo Huangfu, Suxia Yang, Xin Song, Jipeng Qi, Xianjun He, Sihang Wang, Yubin Chen, Qing Yang, Yongxin Song, Yuwen Peng, Guiqian Tang, Jian Gao, Dasa Gu, and Min Shao
Atmos. Chem. Phys., 25, 2459–2472, https://doi.org/10.5194/acp-25-2459-2025, https://doi.org/10.5194/acp-25-2459-2025, 2025
Short summary
Short summary
Online vertical gradient measurements of volatile organic compounds (VOCs), ozone, and NOx were conducted based on a 325 m tall tower in urban Beijing. Vertical changes in the concentrations, compositions, key drivers, and environmental impacts of VOCs were analyzed in this study. We find that VOC species display differentiated vertical variation patterns and distinct roles in contributing to photochemical ozone formation with increasing height in the urban planetary boundary layer.
Shigeyuki Ishidoya, Satoshi Sugawara, and Atsushi Okazaki
Atmos. Chem. Phys., 25, 1965–1987, https://doi.org/10.5194/acp-25-1965-2025, https://doi.org/10.5194/acp-25-1965-2025, 2025
Short summary
Short summary
The 18O/16O ratio of atmospheric oxygen, δatm(18O), is higher than that of ocean water due to isotopic effects during biospheric activities. This is known as the Dole–Morita effect, and its millennial-scale variations are recorded in ice cores. However, small variations of δatm(18O) in the present day have never been detected so far. This paper presents the first observations of diurnal, seasonal, and secular variations in δatm(18O) and applies them to evaluate oxygen, carbon, and water cycles.
Delaney B. Kilgour, Christopher M. Jernigan, Olga Garmash, Sneha Aggarwal, Shengqian Zhou, Claudia Mohr, Matt E. Salter, Joel A. Thornton, Jian Wang, Paul Zieger, and Timothy H. Bertram
Atmos. Chem. Phys., 25, 1931–1947, https://doi.org/10.5194/acp-25-1931-2025, https://doi.org/10.5194/acp-25-1931-2025, 2025
Short summary
Short summary
We report simultaneous measurements of dimethyl sulfide (DMS) and hydroperoxymethyl thioformate (HPMTF) in the eastern North Atlantic. We use an observationally constrained box model to show that cloud loss is the dominant sink of HPMTF in this region over 6 weeks, resulting in large reductions in DMS-derived products that contribute to aerosol formation and growth. Our findings indicate that fast cloud processing of HPMTF must be included in global models to accurately capture the sulfur cycle.
Jiemeng Bao, Xin Zhang, Zhenhai Wu, Li Zhou, Jun Qian, Qinwen Tan, Fumo Yang, Junhui Chen, Yunfeng Li, Hefan Liu, Liqun Deng, and Hong Li
Atmos. Chem. Phys., 25, 1899–1916, https://doi.org/10.5194/acp-25-1899-2025, https://doi.org/10.5194/acp-25-1899-2025, 2025
Short summary
Short summary
We studied carbonyl compounds' role in ozone pollution in the Chengdu Plain Urban Agglomeration, China. During heavy pollution in August 2019, we measured carbonyls at nine sites and analyzed their impact. Areas with higher carbonyl levels, like Chengdu, had worse ozone pollution. While their abundance matters, chemical reactions with other pollutants are the main drivers. Our findings show regional cooperation is vital to reducing ozone pollution effectively.
Baoye Hu, Naihua Chen, Rui Li, Mingqiang Huang, Jinsheng Chen, Youwei Hong, Lingling Xu, Xiaolong Fan, Mengren Li, Lei Tong, Qiuping Zheng, and Yuxiang Yang
Atmos. Chem. Phys., 25, 905–921, https://doi.org/10.5194/acp-25-905-2025, https://doi.org/10.5194/acp-25-905-2025, 2025
Short summary
Short summary
Box modeling with the Master Chemical Mechanism (MCM) was used to explore summertime peroxyacetyl nitrate (PAN) formation and its link to aerosol pollution under high-ozone conditions. The MCM model is effective in the study of PAN photochemical formation and performed better during the clean period than the haze period. Machine learning analysis identified ammonia, nitrate, and fine particulate matter as the top three factors contributing to simulation bias.
Xiansheng Liu, Xun Zhang, Marvin Dufresne, Tao Wang, Lijie Wu, Rosa Lara, Roger Seco, Marta Monge, Ana Maria Yáñez-Serrano, Marie Gohy, Paul Petit, Audrey Chevalier, Marie-Pierre Vagnot, Yann Fortier, Alexia Baudic, Véronique Ghersi, Grégory Gille, Ludovic Lanzi, Valérie Gros, Leïla Simon, Heidi Héllen, Stefan Reimann, Zoé Le Bras, Michelle Jessy Müller, David Beddows, Siqi Hou, Zongbo Shi, Roy M. Harrison, William Bloss, James Dernie, Stéphane Sauvage, Philip K. Hopke, Xiaoli Duan, Taicheng An, Alastair C. Lewis, James R. Hopkins, Eleni Liakakou, Nikolaos Mihalopoulos, Xiaohu Zhang, Andrés Alastuey, Xavier Querol, and Thérèse Salameh
Atmos. Chem. Phys., 25, 625–638, https://doi.org/10.5194/acp-25-625-2025, https://doi.org/10.5194/acp-25-625-2025, 2025
Short summary
Short summary
This study examines BTEX (benzene, toluene, ethylbenzene, xylenes) pollution in urban areas across seven European countries. Analyzing data from 22 monitoring sites, we found traffic and industrial activities significantly impact BTEX levels, with peaks during rush hours. The risk from BTEX exposure remains moderate, especially in high-traffic and industrial zones, highlighting the need for targeted air quality management to protect public health and improve urban air quality.
Yuening Li, Faqiang Zhan, Chubashini Shunthirasingham, Ying Duan Lei, Jenny Oh, Amina Ben Chaaben, Zhe Lu, Kelsey Lee, Frank A. P. C. Gobas, Hayley Hung, and Frank Wania
Atmos. Chem. Phys., 25, 459–472, https://doi.org/10.5194/acp-25-459-2025, https://doi.org/10.5194/acp-25-459-2025, 2025
Short summary
Short summary
Organophosphate esters are important humanmade trace contaminants. Measuring them in the atmospheric gas phase, particles, precipitation, and surface water in Canada, we explore seasonal concentration variability, gas–particle partitioning, precipitation scavenging, and the air–water equilibrium. Whereas higher summer concentrations and efficient precipitation scavenging conform with expectations, the lack of a relationship between compound volatility and gas–particle partitioning is puzzling.
Roeland Van Malderen, Anne M. Thompson, Debra E. Kollonige, Ryan M. Stauffer, Herman G. J. Smit, Eliane Maillard Barras, Corinne Vigouroux, Irina Petropavlovskikh, Thierry Leblanc, Valérie Thouret, Pawel Wolff, Peter Effertz, David W. Tarasick, Deniz Poyraz, Gérard Ancellet, Marie-Renée De Backer, Stéphanie Evan, Victoria Flood, Matthias M. Frey, James W. Hannigan, José L. Hernandez, Marco Iarlori, Bryan J. Johnson, Nicholas Jones, Rigel Kivi, Emmanuel Mahieu, Glen McConville, Katrin Müller, Tomoo Nagahama, Justus Notholt, Ankie Piters, Natalia Prats, Richard Querel, Dan Smale, Wolfgang Steinbrecht, Kimberly Strong, and Ralf Sussmann
EGUsphere, https://doi.org/10.5194/egusphere-2024-3736, https://doi.org/10.5194/egusphere-2024-3736, 2025
Short summary
Short summary
Tropospheric ozone is an important greenhouse gas and is an air pollutant. The time variability of tropospheric ozone is mainly driven by anthropogenic emissions. In this paper, we study the distribution and time variability of ozone from harmonized ground-based observations from five different measurement techniques. Our findings will provide clear standard references for atmospheric models and evolving tropospheric ozone satellite data for the 2000–2022 period.
Fanhao Meng, Baobin Han, Min Qin, Wu Fang, Ke Tang, Dou Shao, Zhitang Liao, Jun Duan, Yan Feng, Yong Huang, Ting Ni, and Pinhua Xie
Atmos. Chem. Phys., 24, 14191–14208, https://doi.org/10.5194/acp-24-14191-2024, https://doi.org/10.5194/acp-24-14191-2024, 2024
Short summary
Short summary
Comprehensive observations of HONO and NOx fluxes were conducted over paddy fields in the Huaihe River Basin. Consecutive peaks in HONO and NO fluxes suggest a potentially enhanced release of HONO and NO due to soil tillage, whereas waterlogged soil may inhibit microbial nitrification processes following irrigation. Notably, biological processes and light-driven NO2 reactions at the surface may serve as sources of HONO and influence the local HONO budget during rotary tillage.
Zhaojin An, Rujing Yin, Xinyan Zhao, Xiaoxiao Li, Yuyang Li, Yi Yuan, Junchen Guo, Yiqi Zhao, Xue Li, Dandan Li, Yaowei Li, Dongbin Wang, Chao Yan, Kebin He, Douglas R. Worsnop, Frank N. Keutsch, and Jingkun Jiang
Atmos. Chem. Phys., 24, 13793–13810, https://doi.org/10.5194/acp-24-13793-2024, https://doi.org/10.5194/acp-24-13793-2024, 2024
Short summary
Short summary
Online Vocus-PTR measurements show the compositions and seasonal variations in organic vapors in urban Beijing. With enhanced sensitivity and mass resolution, various species at a level of sub-parts per trillion (ppt) and organics with multiple oxygens (≥ 3) were observed. The fast photooxidation process in summer leads to an increase in both concentration and proportion of organics with multiple oxygens, while, in other seasons, the variations in them could be influenced by mixed sources.
Bowen Zhang, Dong Zhang, Zhe Dong, Xinshuai Song, Ruiqin Zhang, and Xiao Li
Atmos. Chem. Phys., 24, 13587–13601, https://doi.org/10.5194/acp-24-13587-2024, https://doi.org/10.5194/acp-24-13587-2024, 2024
Short summary
Short summary
To gain insight into the impact of changes due to epidemic control policies, we undertook continuous online monitoring of volatile organic compounds (VOCs) at an urban site in Zhengzhou over a 2-month period. This study examines the characteristics of VOCs, their sources, and their temporal evolution. It also assesses the impact of the policy change on VOC pollution during the monitoring period, thus providing a basis for further research on VOC pollution and source control.
Jakob Boyd Pernov, Jens Liengaard Hjorth, Lise Lotte Sørensen, and Henrik Skov
Atmos. Chem. Phys., 24, 13603–13631, https://doi.org/10.5194/acp-24-13603-2024, https://doi.org/10.5194/acp-24-13603-2024, 2024
Short summary
Short summary
Arctic ozone depletion events (ODEs) occur every spring and have vast implications for the oxidizing capacity, radiative balance, and mercury oxidation. In this study, we analyze ozone, ODEs, and their connection to meteorological and air mass history variables through statistical analyses, back trajectories, and machine learning (ML) at Villum Research Station. ODEs are favorable under sunny, calm conditions with air masses arriving from northerly wind directions with sea ice contact.
Marvin Dufresne, Thérèse Salameh, Thierry Léonardis, Grégory Gille, Alexandre Armengaud, and Stéphane Sauvage
EGUsphere, https://doi.org/10.5194/egusphere-2024-3576, https://doi.org/10.5194/egusphere-2024-3576, 2024
Short summary
Short summary
This paper is about the eighteen-months measurement of Non-Methane Hydrocarbons (NMHC) at Marseille, were there was no measurement since early 2000 despite the impact of NMHC on air quality and climate. The traffic related sources are the first contributor to NMHC concentrations in Marseille and shipping strongly contribute to the formation of aerosols. Finally, the lockdown due to the Covid-19 had an impact on NMHC concentrations reaching a fifty percents decreasing for traffic-related sources.
Hagninou Elagnon Venance Donnou, Aristide Barthélémy Akpo, Money Ossohou, Claire Delon, Véronique Yoboué, Dungall Laouali, Marie Ouafo-Leumbe, Pieter Gideon Van Zyl, Ousmane Ndiaye, Eric Gardrat, Maria Dias-Alves, and Corinne Galy-Lacaux
Atmos. Chem. Phys., 24, 13151–13182, https://doi.org/10.5194/acp-24-13151-2024, https://doi.org/10.5194/acp-24-13151-2024, 2024
Short summary
Short summary
Ozone is a secondary air pollutant that is detrimental to human and plant health. A better understanding of its chemical evolution is a challenge for Africa, where it is still undersampled. Out of 14 sites examined (1995–2020), high levels of O3 are reported in southern Africa. The dominant chemical processes leading to O3 formation are identified. A decrease in O3 is observed at Katibougou (Mali) and Banizoumbou (Niger), and an increase is found at Zoétélé (Cameroon) and Skukuza (South Africa).
Junwei Song, Georgios I. Gkatzelis, Ralf Tillmann, Nicolas Brüggemann, Thomas Leisner, and Harald Saathoff
Atmos. Chem. Phys., 24, 13199–13217, https://doi.org/10.5194/acp-24-13199-2024, https://doi.org/10.5194/acp-24-13199-2024, 2024
Short summary
Short summary
Biogenic volatile organic compounds (BVOCs) and organic aerosol (OA) particles were measured online in a stressed spruce-dominated forest. OA was mainly attributed to the monoterpene oxidation products. The mixing ratios of BVOCs were higher than the values previously measured in other temperate forests. The results demonstrate that BVOCs are influenced not only by meteorology and biogenic emissions but also by local anthropogenic emissions and subsequent chemical transformation processes.
Sachin Mishra, Vinayak Sinha, Haseeb Hakkim, Arpit Awasthi, Sachin D. Ghude, Vijay Kumar Soni, Narendra Nigam, Baerbel Sinha, and Madhavan N. Rajeevan
Atmos. Chem. Phys., 24, 13129–13150, https://doi.org/10.5194/acp-24-13129-2024, https://doi.org/10.5194/acp-24-13129-2024, 2024
Short summary
Short summary
We quantified 111 gases using mass spectrometry to understand how seasonal and emission changes lead from clean air in the monsoon season to extremely polluted air in the post-monsoon season in Delhi. Averaged total mass concentrations (260 µg m-3) were > 4 times in polluted periods, driven by biomass burning emissions and reduced atmospheric ventilation. Reactive gaseous nitrogen, chlorine, and sulfur compounds hitherto unreported from such a polluted environment were discovered.
Gérard Ancellet, Camille Viatte, Anne Boynard, François Ravetta, Jacques Pelon, Cristelle Cailteau-Fischbach, Pascal Genau, Julie Capo, Axel Roy, and Philippe Nédélec
Atmos. Chem. Phys., 24, 12963–12983, https://doi.org/10.5194/acp-24-12963-2024, https://doi.org/10.5194/acp-24-12963-2024, 2024
Short summary
Short summary
Characterization of ozone pollution in urban areas benefited from a measurement campaign in summer 2022 in the Paris region. The analysis is based on 21 d of lidar and aircraft observations. The main objective is an analysis of the sensitivity of ozone pollution to the micrometeorological processes in the urban atmospheric boundary layer and the transport of regional pollution. The paper also discusses to what extent satellite observations can track observed ozone plumes.
Jingwen Dai, Kun Zhang, Yanli Feng, Xin Yi, Rui Li, Jin Xue, Qing Li, Lishu Shi, Jiaqiang Liao, Yanan Yi, Fangting Wang, Liumei Yang, Hui Chen, Ling Huang, Jiani Tan, Yangjun Wang, and Li Li
EGUsphere, https://doi.org/10.5194/egusphere-2024-3201, https://doi.org/10.5194/egusphere-2024-3201, 2024
Short summary
Short summary
Oxygenated volatile organic compounds (OVOCs) are important ozone (O3) precursors. However, most of O3 formation analysis based on the box model (OBM) don't include OVOCs constraint To access the interference of OVOCs on O3 simulation, this study conducted field campaign and OBM analysis. The results indicates that no OVOCs constraint in the OBM can lead to overestimate of OVOCs, free radicals, and O3.
Simone T. Andersen, Rolf Sander, Patrick Dewald, Laura Wüst, Tobias Seubert, Gunther N. T. E. Türk, Jan Schuladen, Max R. McGillen, Chaoyang Xue, Abdelwahid Mellouki, Alexandre Kukui, Vincent Michoud, Manuela Cirtog, Mathieu Cazaunau, Astrid Bauville, Hichem Bouzidi, Paola Formenti, Cyrielle Denjean, Jean-Claude Etienne, Olivier Garrouste, Christopher Cantrell, Jos Lelieveld, and John N. Crowley
EGUsphere, https://doi.org/10.5194/egusphere-2024-3437, https://doi.org/10.5194/egusphere-2024-3437, 2024
Short summary
Short summary
Measurements and modelling of reactive nitrogen gases observed in a suburban temperate forest in Rambouillet, France circa 50 km southwest of Paris in 2022 indicate that the biosphere rapidly scavenges organic nitrates of mixed biogenic and anthropogenic origin, resulting in short lifetimes for e.g. alkyl nitrates and peroxy nitrates.
Xiaoyi Zhang, Wanyun Xu, Weili Lin, Gen Zhang, Jinjian Geng, Li Zhou, Huarong Zhao, Sanxue Ren, Guangsheng Zhou, Jianmin Chen, and Xiaobin Xu
Atmos. Chem. Phys., 24, 12323–12340, https://doi.org/10.5194/acp-24-12323-2024, https://doi.org/10.5194/acp-24-12323-2024, 2024
Short summary
Short summary
Ozone (O3) deposition is a key process that removes surface O3, affecting air quality, ecosystems and climate change. We conducted O3 deposition measurement over a wheat canopy using a newly relaxed eddy accumulation flux system. Large variabilities in O3 deposition were detected, mainly determined by crop growth and modulated by various environmental factors. More O3 deposition observations over different surfaces are needed for exploring deposition mechanisms and model optimization.
Honglei Wang, David W. Tarasick, Jane Liu, Herman G. J. Smit, Roeland Van Malderen, Lijuan Shen, Romain Blot, and Tianliang Zhao
Atmos. Chem. Phys., 24, 11927–11942, https://doi.org/10.5194/acp-24-11927-2024, https://doi.org/10.5194/acp-24-11927-2024, 2024
Short summary
Short summary
In this study, we identify 23 suitable pairs of sites from World Ozone and Ultraviolet Radiation Data Centre (WOUDC) and In-service Aircraft for a Global Observing System (IAGOS) datasets (1995 to 2021), compare the average vertical distributions of tropospheric O3 from ozonesonde and aircraft measurements, and analyze the differences based on ozonesonde type and station–airport distance.
Noémie Taquet, Wolfgang Stremme, María Eugenia González del Castillo, Victor Almanza, Alejandro Bezanilla, Olivier Laurent, Carlos Alberti, Frank Hase, Michel Ramonet, Thomas Lauvaux, Ke Che, and Michel Grutter
Atmos. Chem. Phys., 24, 11823–11848, https://doi.org/10.5194/acp-24-11823-2024, https://doi.org/10.5194/acp-24-11823-2024, 2024
Short summary
Short summary
We characterize the variability in CO and CO2 emissions over Mexico City from long-term time-resolved Fourier transform infrared spectroscopy solar absorption and surface measurements from 2013 to 2021. Using the average intraday CO growth rate from total columns, the average CO / CO2 ratio and TROPOMI data, we estimate the interannual variability in the CO and CO2 anthropogenic emissions of Mexico City, highlighting the effect of an unprecedented drop in activity due to the COVID-19 lockdown.
Akima Ringsdorf, Achim Edtbauer, Bruna Holanda, Christopher Poehlker, Marta O. Sá, Alessandro Araújo, Jürgen Kesselmeier, Jos Lelieveld, and Jonathan Williams
Atmos. Chem. Phys., 24, 11883–11910, https://doi.org/10.5194/acp-24-11883-2024, https://doi.org/10.5194/acp-24-11883-2024, 2024
Short summary
Short summary
We show the average height distribution of separately observed aldehydes and ketones over a day and discuss their rainforest-specific sources and sinks as well as their seasonal changes above the Amazon. Ketones have much longer atmospheric lifetimes than aldehydes and thus different implications for atmospheric chemistry. However, they are commonly observed together, which we overcome by measuring with a NO+ chemical ionization mass spectrometer for the first time in the Amazon rainforest.
Theresa Harlass, Rebecca Dischl, Stefan Kaufmann, Raphael Märkl, Daniel Sauer, Monika Scheibe, Paul Stock, Tiziana Bräuer, Andreas Dörnbrack, Anke Roiger, Hans Schlager, Ulrich Schumann, Magdalena Pühl, Tobias Schripp, Tobias Grein, Linda Bondorf, Charles Renard, Maxime Gauthier, Mark Johnson, Darren Luff, Paul Madden, Peter Swann, Denise Ahrens, Reetu Sallinen, and Christiane Voigt
Atmos. Chem. Phys., 24, 11807–11822, https://doi.org/10.5194/acp-24-11807-2024, https://doi.org/10.5194/acp-24-11807-2024, 2024
Short summary
Short summary
Emissions from aircraft have a direct impact on our climate. Here, we present airborne and ground-based measurement data of nitrogen oxides that were collected in the exhaust of an Airbus aircraft. We study the impact of burning fossil and sustainable aviation fuel on nitrogen oxide emissions at different engine settings related to combustor temperature, pressure and fuel flow. Further, we compare observations with engine emission models.
Zhouxing Zou, Tianshu Chen, Qianjie Chen, Weihang Sun, Shichun Han, Zhuoyue Ren, Xinyi Li, Wei Song, Aoqi Ge, Qi Wang, Xiao Tian, Chenglei Pei, Xinming Wang, Yanli Zhang, and Tao Wang
EGUsphere, https://doi.org/10.5194/egusphere-2024-3210, https://doi.org/10.5194/egusphere-2024-3210, 2024
Short summary
Short summary
We measured ambient OH and HO2 concentrations at a subtropical rural site and compared our observations with model results. During warm periods, the model overestimated the concentrations of OH and HO2, leading to overestimation of ozone and nitric acid production. Our findings highlight the need to better understand how OH and HO2are formed and removed, which is important for accurate air quality and climate predictions.
Simone T. Andersen, Max R. McGillen, Chaoyang Xue, Tobias Seubert, Patrick Dewald, Gunther N. T. E. Türk, Jan Schuladen, Cyrielle Denjean, Jean-Claude Etienne, Olivier Garrouste, Marina Jamar, Sergio Harb, Manuela Cirtog, Vincent Michoud, Mathieu Cazaunau, Antonin Bergé, Christopher Cantrell, Sebastien Dusanter, Bénédicte Picquet-Varrault, Alexandre Kukui, Abdelwahid Mellouki, Lucy J. Carpenter, Jos Lelieveld, and John N. Crowley
Atmos. Chem. Phys., 24, 11603–11618, https://doi.org/10.5194/acp-24-11603-2024, https://doi.org/10.5194/acp-24-11603-2024, 2024
Short summary
Short summary
Using measurements of various trace gases in a suburban forest near Paris in the summer of 2022, we were able to gain insight into the sources and sinks of NOx (NO+NO2) with a special focus on their nighttime chemical and physical loss processes. NO was observed as a result of nighttime soil emissions when O3 levels were strongly depleted by deposition. NO oxidation products were not observed at night, indicating that soil and/or foliar surfaces are an efficient sink of reactive N.
Lee Tiszenkel, James H. Flynn, and Shan-Hu Lee
Atmos. Chem. Phys., 24, 11351–11363, https://doi.org/10.5194/acp-24-11351-2024, https://doi.org/10.5194/acp-24-11351-2024, 2024
Short summary
Short summary
Ammonia and amines are important ingredients for aerosol formation in urban environments, but the measurements of these compounds are extremely challenging. Our observations show that urban ammonia and amines in Houston are emitted from urban sources, and diurnal variations in their concentrations are likely governed by gas-to-particle conversion and emissions.
Arpit Awasthi, Baerbel Sinha, Haseeb Hakkim, Sachin Mishra, Varkrishna Mummidivarapu, Gurmanjot Singh, Sachin D. Ghude, Vijay Kumar Soni, Narendra Nigam, Vinayak Sinha, and Madhavan N. Rajeevan
Atmos. Chem. Phys., 24, 10279–10304, https://doi.org/10.5194/acp-24-10279-2024, https://doi.org/10.5194/acp-24-10279-2024, 2024
Short summary
Short summary
We use 111 volatile organic compounds (VOCs), PM10, and PM2.5 in a positive matrix factorization (PMF) model to resolve 11 pollution sources validated with chemical fingerprints. Crop residue burning and heating account for ~ 50 % of the PM, while traffic and industrial emissions dominate the gas-phase VOC burden and formation potential of secondary organic aerosols (> 60 %). Non-tailpipe emissions from compressed-natural-gas-fuelled commercial vehicles dominate the transport sector's PM burden.
Luke D. Schiferl, Cong Cao, Bronte Dalton, Andrew Hallward-Driemeier, Ricardo Toledo-Crow, and Róisín Commane
Atmos. Chem. Phys., 24, 10129–10142, https://doi.org/10.5194/acp-24-10129-2024, https://doi.org/10.5194/acp-24-10129-2024, 2024
Short summary
Short summary
Carbon monoxide (CO) is an air pollutant and an important indicator of the incomplete combustion of fossil fuels in cities. Using 4 years of winter and spring observations in New York City, we found that both the magnitude and variability of CO from the metropolitan area are greater than expected. Transportation emissions cannot explain the missing and variable CO, which points to energy from buildings as a likely underappreciated source of urban air pollution and greenhouse gas emissions.
Chengzhi Xing, Cheng Liu, Chunxiang Ye, Jingkai Xue, Hongyu Wu, Xiangguang Ji, Jinping Ou, and Qihou Hu
Atmos. Chem. Phys., 24, 10093–10112, https://doi.org/10.5194/acp-24-10093-2024, https://doi.org/10.5194/acp-24-10093-2024, 2024
Short summary
Short summary
We identified the contributions of ozone (O3) and nitrous acid (HONO) to the production rates of hydroxide (OH) in vertical space on the Tibetan Plateau (TP). A new insight was offered: the contributions of HONO and O3 to the production rates of OH on the TP are even greater than in lower-altitudes areas. This study enriches the understanding of vertical distribution of atmospheric components and explains the strong atmospheric oxidation capacity (AOC) on the TP.
Pengfei Han, Ning Zeng, Bo Yao, Wen Zhang, Weijun Quan, Pucai Wang, Ting Wang, Minqiang Zhou, Qixiang Cai, Yuzhong Zhang, Ruosi Liang, Wanqi Sun, and Shengxiang Liu
EGUsphere, https://doi.org/10.5194/egusphere-2024-2162, https://doi.org/10.5194/egusphere-2024-2162, 2024
Short summary
Short summary
Methane (CH4) is a potent greenhouse gas. Northern China contributes a large proportion of CH4 emissions yet large observation gaps are existed. Here we compiled a comprehensive dataset which is publicly available including ground-based, satellite-based, inventory and modeling results, to show the CH4 concentrations, enhancements and spatial-temporal variations. The data can benefit the research community, and policy makers for future observations, atmospheric inversions and policy-making.
Xinyuan Zhang, Lingling Wang, Nan Wang, Shuangliang Ma, Shenbo Wang, Ruiqin Zhang, Dong Zhang, Mingkai Wang, and Hongyu Zhang
Atmos. Chem. Phys., 24, 9885–9898, https://doi.org/10.5194/acp-24-9885-2024, https://doi.org/10.5194/acp-24-9885-2024, 2024
Short summary
Short summary
This study highlights the importance of the redox reaction of NO2 with SO2 based on actual atmospheric observations. The particle pH in future China is expected to rise steadily. Consequently, this reaction could become a significant source of HONO in China. Therefore, it is crucial to coordinate the control of SO2, NOx, and NH3 emissions to avoid a rapid increase in the particle pH.
Jun Zhou, Chunsheng Zhang, Aiming Liu, Bin Yuan, Yan Wang, Wenjie Wang, Jie-Ping Zhou, Yixin Hao, Xiao-Bing Li, Xianjun He, Xin Song, Yubin Chen, Suxia Yang, Shuchun Yang, Yanfeng Wu, Bin Jiang, Shan Huang, Junwen Liu, Yuwen Peng, Jipeng Qi, Minhui Deng, Bowen Zhong, Yibo Huangfu, and Min Shao
Atmos. Chem. Phys., 24, 9805–9826, https://doi.org/10.5194/acp-24-9805-2024, https://doi.org/10.5194/acp-24-9805-2024, 2024
Short summary
Short summary
In-depth understanding of the near-ground vertical variability in photochemical ozone (O3) formation is crucial for mitigating O3 pollution. Utilizing a self-built vertical observation system, a direct net photochemical O3 production rate detection system, and an observation-based model, we diagnosed the vertical distributions and formation mechanism of net photochemical O3 production rates and sensitivity in the Pearl River Delta region, one of the most O3-polluted areas in China.
Eleanor J. Derry, Tyler R. Elgiar, Taylor Y. Wilmot, Nicholas W. Hoch, Noah S. Hirshorn, Peter Weiss-Penzias, Christopher F. Lee, John C. Lin, A. Gannet Hallar, Rainer Volkamer, Seth N. Lyman, and Lynne E. Gratz
Atmos. Chem. Phys., 24, 9615–9643, https://doi.org/10.5194/acp-24-9615-2024, https://doi.org/10.5194/acp-24-9615-2024, 2024
Short summary
Short summary
Mercury (Hg) is a globally distributed neurotoxic pollutant. Atmospheric deposition is the main source of Hg in ecosystems. However, measurement biases hinder understanding of the origins and abundance of the more bioavailable oxidized form. We used an improved, calibrated measurement system to study air mass composition and transport of atmospheric Hg at a remote mountaintop site in the central US. Oxidized Hg originated upwind in the low to middle free troposphere under clean, dry conditions.
Benjamin A. Nault, Katherine R. Travis, James H. Crawford, Donald R. Blake, Pedro Campuzano-Jost, Ronald C. Cohen, Joshua P. DiGangi, Glenn S. Diskin, Samuel R. Hall, L. Gregory Huey, Jose L. Jimenez, Kyung-Eun Min, Young Ro Lee, Isobel J. Simpson, Kirk Ullmann, and Armin Wisthaler
Atmos. Chem. Phys., 24, 9573–9595, https://doi.org/10.5194/acp-24-9573-2024, https://doi.org/10.5194/acp-24-9573-2024, 2024
Short summary
Short summary
Ozone (O3) is a pollutant formed from the reactions of gases emitted from various sources. In urban areas, the density of human activities can increase the O3 formation rate (P(O3)), thus impacting air quality and health. Observations collected over Seoul, South Korea, are used to constrain P(O3). A high local P(O3) was found; however, local P(O3) was partly reduced due to compounds typically ignored. These observations also provide constraints for unmeasured compounds that will impact P(O3).
Fan Zhang, Binyu Xiao, Zeyu Liu, Yan Zhang, Chongguo Tian, Rui Li, Can Wu, Yali Lei, Si Zhang, Xinyi Wan, Yubao Chen, Yong Han, Min Cui, Cheng Huang, Hongli Wang, Yingjun Chen, and Gehui Wang
Atmos. Chem. Phys., 24, 8999–9017, https://doi.org/10.5194/acp-24-8999-2024, https://doi.org/10.5194/acp-24-8999-2024, 2024
Short summary
Short summary
Mandatory use of low-sulfur fuel due to global sulfur limit regulations means large uncertainties in volatile organic compound (VOC) emissions. On-board tests of VOCs from nine cargo ships in China were carried out. Results showed that switching from heavy-fuel oil to diesel increased emission factor VOCs by 48 % on average, enhancing O3 and the secondary organic aerosol formation potential. Thus, implementing a global ultra-low-sulfur oil policy needs to be optimized in the near future.
Patrick Dewald, Tobias Seubert, Simone T. Andersen, Gunther N. T. E. Türk, Jan Schuladen, Max R. McGillen, Cyrielle Denjean, Jean-Claude Etienne, Olivier Garrouste, Marina Jamar, Sergio Harb, Manuela Cirtog, Vincent Michoud, Mathieu Cazaunau, Antonin Bergé, Christopher Cantrell, Sebastien Dusanter, Bénédicte Picquet-Varrault, Alexandre Kukui, Chaoyang Xue, Abdelwahid Mellouki, Jos Lelieveld, and John N. Crowley
Atmos. Chem. Phys., 24, 8983–8997, https://doi.org/10.5194/acp-24-8983-2024, https://doi.org/10.5194/acp-24-8983-2024, 2024
Short summary
Short summary
In the scope of a field campaign in a suburban forest near Paris in the summer of 2022, we measured the reactivity of the nitrate radical NO3 towards biogenic volatile organic compounds (BVOCs; e.g. monoterpenes) mainly below but also above the canopy. NO3 reactivity was the highest during nights with strong temperature inversions and decreased strongly with height. Reactions with BVOCs were the main removal process of NO3 throughout the diel cycle below the canopy.
Jian Wang, Lei Xue, Qianyao Ma, Feng Xu, Gaobin Xu, Shibo Yan, Jiawei Zhang, Jianlong Li, Honghai Zhang, Guiling Zhang, and Zhaohui Chen
Atmos. Chem. Phys., 24, 8721–8736, https://doi.org/10.5194/acp-24-8721-2024, https://doi.org/10.5194/acp-24-8721-2024, 2024
Short summary
Short summary
This study investigated the distribution and sources of non-methane hydrocarbons (NMHCs) in the lower atmosphere over the marginal seas of China. NMHCs, a subset of volatile organic compounds (VOCs), play a crucial role in atmospheric chemistry. Derived from systematic atmospheric sampling in coastal cities and marginal sea regions, this study offers valuable insights into the interaction between land and sea in shaping offshore atmospheric NMHCs.
Yusheng Zhang, Feixue Zheng, Zemin Feng, Chaofan Lian, Weigang Wang, Xiaolong Fan, Wei Ma, Zhuohui Lin, Chang Li, Gen Zhang, Chao Yan, Ying Zhang, Veli-Matti Kerminen, Federico Bianch, Tuukka Petäjä, Juha Kangasluoma, Markku Kulmala, and Yongchun Liu
Atmos. Chem. Phys., 24, 8569–8587, https://doi.org/10.5194/acp-24-8569-2024, https://doi.org/10.5194/acp-24-8569-2024, 2024
Short summary
Short summary
The nitrous acid (HONO) budget was validated during a COVID-19 lockdown event. The main conclusions are (1) HONO concentrations showed a significant decrease from 0.97 to 0.53 ppb during lockdown; (2) vehicle emissions accounted for 53 % of nighttime sources, with the heterogeneous conversion of NO2 on ground surfaces more important than aerosol; and (3) the dominant daytime source shifted from the homogenous reaction between NO and OH (51 %) to nitrate photolysis (53 %) during lockdown.
Dong Zhang, Xiao Li, Minghao Yuan, Yifei Xu, Qixiang Xu, Fangcheng Su, Shenbo Wang, and Ruiqin Zhang
Atmos. Chem. Phys., 24, 8549–8567, https://doi.org/10.5194/acp-24-8549-2024, https://doi.org/10.5194/acp-24-8549-2024, 2024
Short summary
Short summary
The increasing concentration of O3 precursors and unfavorable meteorological conditions are key factors in the formation of O3 pollution in Zhengzhou. Vehicular exhausts (28 %), solvent usage (27 %), and industrial production (22 %) are identified as the main sources of NMVOCs. Moreover, O3 formation in Zhengzhou is found to be in an anthropogenic volatile organic compound (AVOC)-limited regime. Thus, to reduce O3 formation, a minimum AVOCs / NOx reduction ratio ≥ 3 : 1 is recommended.
Arianna Peron, Martin Graus, Marcus Striednig, Christian Lamprecht, Georg Wohlfahrt, and Thomas Karl
Atmos. Chem. Phys., 24, 7063–7083, https://doi.org/10.5194/acp-24-7063-2024, https://doi.org/10.5194/acp-24-7063-2024, 2024
Short summary
Short summary
The anthropogenic fraction of non-methane volatile organic compound (NMVOC) emissions associated with biogenic sources (e.g., terpenes) is investigated based on eddy covariance observations. The anthropogenic fraction of terpene emissions is strongly dependent on season. When analyzing volatile chemical product (VCP) emissions in urban environments, we caution that observations from short-term campaigns might over-/underestimate their significance depending on local and seasonal circumstances.
Cited articles
Barnes, I., Hjorth, J., and Mihalopoulos, N.: Dimethylsulfide and dimethylsulfoxide and their oxidation in the atmosphere, Chem. Rev., 106, 940–975, https://doi.org/10.1021/Cr020529, 2006.
Bourassa, A. E., Robock, A., Randel, W. J., Deshler, T., Rieger, L. A., Lloyd, N. D., Llewellyn, E. J., and Degenstein, D. A.: Large volcanic aerosol load in the stratosphere linked to asian monsoon transport, Science, 337, 78–81, https://doi.org/10.1126/science.1219371, 2012.
Brühl, C., Lelieveld, J., Crutzen, P. J., and Tost, H.: The role of carbonyl sulphide as a source of stratospheric sulphate aerosol and its impact on climate, Atmos. Chem. Phys., 12, 1239–1253, https://doi.org/10.5194/acp-12-1239-2012, 2012.
Charlson, R. J., Lovelock, J. E., Andreae, M. O., and Warren, S. G.: Oceanic phytoplankton, atmospheric sulfur, cloud albedo and climate, Nature, 326, 655–661, https://doi.org/10.1038/326655a0, 1987.
Chatfield, R. B. and Crutzen, P. J.: Sulfur-dioxide in remote oceanic air – Cloud transport of reactive precursors, J. Geophys. Res.-Atmos., 89, 7111–7132, https://doi.org/10.1029/Jd089id05p07111, 1984.
Corti, T., Luo, B. P.,de Rues, M., Brunner, D., Cairo, F., Mahoney, M. J., Martucci, G., Matthez, R., Mitev, V., dos Santos, F. H., Schiller, C., Shur, G., Sitnikov, N. M., Spetlen, N., Vössing, J. J., Borrmann, S., and Peter, T.: Unprecedented evidence for deep convection hydrating the tropical stratosphere, Geophys. Res. Lett., 35, L10810, https://doi.org/10.1029/2008GL033641, 2008.
Crutzen, P. J.: The possible importance of OCS for the sulfate layer of the stratosphere, Geophys. Res. Lett., 3, 73–76, https://doi.org/10.1029/Gl003i002p00073, 1976.
Dee, D. P., Uppala, S. M., Simmons, A. J., Berrisford, P., Poli, P., Kobayashi, S., Andrae, U., Balmaseda, M. A., Balsamo, G., Bauer, P., Bechtold, P., Beljaars, A. C. M., van de Berg, L., Bidlot, J., Bormann, N., Delsol, C., Dragani, R., Fuentes, M., Geer, A. J., Haimberger, L., Healy, S. B., Hersbach, H., Holm, E. V., Isaksen, L., Kallberg, P., Kohler, M., Matricardi, M., McNally, A. P., Monge-Sanz, B. M., Morcrette, J. J., Park, B. K., Peubey, C., de Rosnay, P., Tavolato, C., Thepaut, J. N., and Vitart, F.: The ERA-Interim reanalysis: configuration and performance of the data assimilation system, Q. J. Roy. Meteor. Soc., 137, 553–597, https://doi.org/10.1002/Qj.828, 2011.
Draxler, R. R. and Hess, G. D.: Description of the hysplit 4 modeling system.NOAA Technical Memorandum, ERL, ARL–224, 27, available at: http://www.arl.noaa.gov/documents/reports/arl-224.pdf, 2004.
Forster, C., Wandinger, U., Wotawa, G., James, P., Mattis, I., Althausen, D., Simmonds, P., O'Doherty, S., Jennings, S. G., Kleefeld, C., Schneider, J., Trickl, T., Kreipl, S., Jager, H., and Stohl, A.: Transport of boreal forest fire emissions from Canada to Europe, J. Geophys. Res.-Atmos., 106, 22887–22906, https://doi.org/10.1029/2001jd900115, 2001.
Forster, C., Cooper, O., Stohl, A., Eckhardt, S., James, P., Dunlea, E., Nicks, D. K., Holloway, J. S., Hubler, G., Parrish, D. D., Ryerson, T. B., and Trainer, M.: Lagrangian transport model forecasts and a transport climatology for the Intercontinental Transport and Chemical Transformation 2002 (ITCT 2K2) measurement campaign, J. Geophys. Res.-Atmos., 109, D07s92, https://doi.org/10.1029/2003jd003589, 2004.
Forster, C., Stohl, A., and Seibert, P.: Parameterization of convective transport in a Lagrangian particle dispersion model and its evaluation, J Appl. Meteorol. Clim., 46, 403–422, https://doi.org/10.1175/Jam2470.1, 2007.
Froyd, K. D., Murphy, D. M., Sanford, T. J., Thomson, D. S., Wilson, J. C., Pfister, L., and Lait, L.: Aerosol composition of the tropical upper troposphere, Atmos. Chem. Phys., 9, 4363–4385, https://doi.org/10.5194/acp-9-4363-2009, 2009.
Fueglistaler, S. and Haynes, P. H.: Control of interannual and longer-term variability of stratospheric water vapor, J. Geophys. Res.-Atmos., 110, D24108, https://doi.org/10.1029/2005jd006019, 2005.
Fueglistaler, S., Dessler, A. E., Dunkerton, T. J., Folkins, I., Fu, Q., and Mote, P. W.: Tropical Tropopause Layer, Rev. Geophys., 47, Rg1004, https://doi.org/10.1029/2008rg000267, 2009.
Gettelman, A., Salby, M., and Sassi, F.: Distribution and influenceof convection in the tropical tropopause region, J. Geophys. Res.-Atmos., 107, 4080, https://doi.org/10.1029/2001JD001048, 2002.
Gondwe, M., Krol, M., Gieskes, W., Klaassen, W., and de Baar, H.: The contribution of ocean-leaving DMS to the global atmospheric burdens of DMS, MSA, SO2, and NSS SO$_4^=$, Global Biogeochem. Cy., 17, 1056, https://doi.org/10.1029/2002gb001937, 2003.
Ho, D. T., Law, C. S., Smith, M. J., Schlosser, P., Harvey, M., and Hill, P.: Measurements of air-sea gas exchange at high wind speeds in the Southern Ocean: Implications for global parameterizations, Geophys. Res. Lett., 33, L16611, https://doi.org/10.1029/2006gl026817, 2006.
Hofmann, D., Barnes, J., O'Neill, M., Trudeau, M., and Neely, R.: Increase in background stratospheric aerosol observed with lidar at Mauna Loa Observatory and Boulder, Colorado, Geophys. Res. Lett., 36, L15808, https://doi.org/10.1029/2009gl039008, 2009.
Kato, S., Ui, T., Uematsu, M., and Kajii, Y.: Trace gas measurements over the northwest Pacific during the 2002 IOC cruise, Geochem. Geophy. Geosy., 8, Q06m10, https://doi.org/10.1029/2006gc001241, 2007.
Kettle, A. J. and Andreae, M. O.: Flux of dimethylsulfide from the oceans: A comparison of updated data seas and flux models, J. Geophys. Res.-Atmos., 105, 26793–26808, https://doi.org/10.1029/2000jd900252, 2000.
Kettle, A. J., Andreae, M. O., Amouroux, D., Andreae, T. W., Bates, T. S., Berresheim, H., Bingemer, H., Boniforti, R., Curran, M. A. J., DiTullio, G. R., Helas, G., Jones, G. B., Keller, M. D., Kiene, R. P., Leck, C., Levasseur, M., Malin, G., Maspero, M., Matrai, P., McTaggart, A. R., Mihalopoulos, N., Nguyen, B. C., Novo, A., Putaud, J. P., Rapsomanikis, S., Roberts, G., Schebeske, G., Sharma, S., Simo, R., Staubes, R., Turner, S., and Uher, G.: A global database of sea surface dimethylsulfide (DMS) measurements and a procedure to predict sea surface DMS as a function of latitude, longitude, and month, Global Biogeochem. Cy., 13, 399–444, https://doi.org/10.1029/1999gb900004, 1999.
Krüger, K. and Quack, B.: Introduction to special issue: the TransBrom Sonne expedition in the tropical West Pacific, Atmos. Chem. Phys. Discuss., 12, 1401–1418, https://doi.org/10.5194/acpd-12-1401-2012, 2012.
Krüger, K., Tegtmeier, S., and Rex, M.: Long-term climatology of air mass transport through the Tropical Tropopause Layer (TTL) during NH winter, Atmos. Chem. Phys., 8, 813–823, https://doi.org/10.5194/acp-8-813-2008, 2008.
Krüger, K., Tegtmeier, S., and Rex, M.: Variability of residence time in the Tropical Tropopause Layer during Northern Hemisphere winter, Atmos. Chem. Phys., 9, 6717–6725, https://doi.org/10.5194/acp-9-6717-2009, 2009.
Lana, A., Bell, T. G., Simo, R., Vallina, S. M., Ballabrera-Poy, J., Kettle, A. J., Dachs, J., Bopp, L., Saltzman, E. S., Stefels, J., Johnson, J. E., and Liss, P. S.: An updated climatology of surface dimethlysulfide concentrations and emission fluxes in the global ocean, Global Biogeochem. Cy., 25, Gb1004, https://doi.org/10.1029/2010gb003850, 2011.
Liss, P. S. and Merlivat, L.: Air-sea gas exchange rates: introduction and synthesis, in: The role of air-sea exchange in geochemical cycling, edited by: Buat-Ménard, P., Dordrecht, 113–128, 1986.
Liu, C. T. and Zipser, E. J.: Global distribution of convection penetrating the tropical tropopause, J. Geophys. Res.-Atmos., 110, D23104, https://doi.org/10.1029/2005JD006063, 2005.
Lucas, D. D. and Prinn, R. G.: Tropospheric distributions of sulfuric acid-water vapor aerosol nucleation rates from dimethylsulfide oxidation, Geophys. Res. Lett., 30, 2136, https://doi.org/10.1029/2003gl018370, 2003.
Marandino, C. A., De Bruyn, W. J., Miller, S. D., and Saltzman, E. S.: Eddy correlation measurements of the air/sea flux of dimethylsulfide over the North Pacific Ocean, J. Geophys. Res.-Atmos., 112, D03301, https://doi.org/10.1029/2006jd007293, 2007.
Marandino, C. A., De Bruyn, W. J., Miller, S. D., and Saltzman, E. S.: DMS air/sea flux and gas transfer coefficients from the North Atlantic summertime coccolithophore bloom, Geophys. Res. Lett., 35, L23812, https://doi.org/10.1029/2008gl036370, 2008.
Myhre, G., Berglen, T. F., Myhre, C. E. L., and Isaksen, I. S. A.: The radiative effect of the anthropogenic influence on the stratospheric sulfate aerosol layer, Tellus B, 56, 294–299, https://doi.org/10.1111/j.1600-0889.2004.00106.x, 2004.
Nazaryan, H., McCormick, M. P., and Menzel, W. P.: Global characterization of cirrus clouds using CALIPSO data, J. Geophys. Res.-Atmos., 113, D16211, https://doi.org/10.1029/2007JD009481, 2008.
Newell, R. E. and Gould-Stewart, S.: A stratospheric fountain?, J. Atmos. Sci., 38, 2789–2796, 1981.
Osthoff, H. D., Bates, T. S., Johnson, J. E., Kuster, W. C., Goldan, P., Sommariva, R., Williams, E. J., Lerner, B. M., Warneke, C., de Gouw, J. A., Pettersson, A., Baynard, T., Meagher, J. F., Fehsenfeld, F. C., Ravishankara, A. R., and Brown, S. S.: Regional variation of the dimethyl sulfide oxidation mechanism in the summertime marine boundary layer in the Gulf of Maine, J. Geophys. Res.-Atmos., 114, D07301, https://doi.org/10.1029/2008jd010990, 2009.
Rex, M., Ridder, T., Notholt, J., Immler, F., Lehmann, R., Krüger, K., Mohr, V., und Tegtmeier, S.: Is there a hole in the global OH shield over the tropical Western Pacific warm pool?, Quadrennial Ozone Symposium, Toronto, 2012.
Ricaud, P., Barret, B., Attié, L., Motte, E., Le Flochmoën, E., Teyssèdre, H., Peuch, V.-H., Livesey, N., Lambert, A., and Pommereau, J.-P.: Impact of land convection on troposphere-stratosphere exchange in the tropics, Atmos. Chem. Phys., 7, 5639–5657, https://doi.org/10.5194/acp-7-5639-2007, 2007.
Romps, D. M. and Kuang, Z.: Overshooting convection in tropical cyclones, Geophys. Res. Lett., 36, L09804, https://doi.org/10.1029/2009GL037396, 2009.
Rossow, W. B. and Pearl, C.: 22-Year survey of tropical convection penetrating into the lower stratosphere, Geophys. Res. Lett., 34, L04803, https://doi.org/10.1029/2006GL028635, 2007.
Saltzman, E. S., King, D. B., Holmen, K., and Leck, C.: Experimental determination of the diffusion coefficient of dimethylsulfide in water, J. Geophys. Res., 98, 16481–16486, https://doi.org/10.1029/93JC01858, 1993.
Sassen, K., Wang, Z., and Liu, D.: Global distribution of cirrus clouds from CloudSat/CloudAerosol Lidar and Infrared Pathfinder Satellite Observations (CALIPSO) measurements, J. Geophys. Res.-Atmos., 113, D00A12, https://doi.org/10.1029/2008JD009972, 2008.
Schauffler, S. M., Atlas, E. L., Blake, D. R., Flocke, F., Lueb, R. A., Lee-Taylor, J. M., Stroud, V., and Travnicek, W.: Distributions of brominated organic compounds in the troposphere and lower stratosphere, J. Geophys. Res.-Atmos., 104, 21513–21535, https://doi.org/10.1029/1999jd900197, 1999.
Solomon, S., Daniel, J. S., Neely, R. R., Vernier, J. P., Dutton, E. G., and Thomason, L. W.: The persistently variable "background" stratospheric aerosol layer and global climate change, Science, 333, 866–870, https://doi.org/10.1126/science.1206027, 2011.
Spichtinger, N., Wenig, M., James, P., Wagner, T., Platt, U., and Stohl, A.: Satellite detection of a continental-scale plume of nitrogen oxides from boreal forest fires, Geophys. Res. Lett., 28, 4579–4582, https://doi.org/10.1029/2001GL013484, 2001.
Stohl, A., and Thomson, D. J.: A density correction for Lagrangian particle dispersion models, Bound-Lay Meteorol., 90, 155–167, https://doi.org/10.1023/A:1001741110696, 1999.
Stohl, A. and Trickl, T.: A textbook example of long-range transport: Simultaneous observation of ozone maxima of stratospheric and North American origin in the free troposphere over Europe, J. Geophys. Res.-Atmos., 104, 30445–30462, https://doi.org/10.1029/1999jd900803, 1999.
Stohl, A., Hittenberger, M., and Wotawa, G.: Validation of the Lagrangian particle dispersion model FLEXPART against large-scale tracer experiment data, Atmos. Environ., 32, 4245–4264, https://doi.org/10.1016/S1352-2310(98)00184-8, 1998.
Stohl, A., Forster, C., Eckhardt, S., Spichtinger, N., Huntrieser, H., Heland, J., Schlager, H., Wilhelm, S., Arnold, F., and Cooper, O.: A backward modeling study of intercontinental pollution transport using aircraft measurements, J. Geophys. Res.-Atmos., 108, 4370, https://doi.org/10.1029/2002jd002862, 2003.
Stohl, A., Forster, C., Frank, A., Seibert, P., and Wotawa, G.: Technical note: The Lagrangian particle dispersion model FLEXPART version 6.2, Atmos. Chem. Phys., 5, 2461–2474, https://doi.org/10.5194/acp-5-2461-2005, 2005.
Tegtmeier, S., Krüger, K., Quack, B., Atlas, E. L., Pisso, I., Stohl, A., and Yang, X.: Emission and transport of bromocarbons: from the West Pacific ocean into the stratosphere, Atmos. Chem. Phys., 12, 10633–10648, https://doi.org/10.5194/acp-12-10633-2012, 2012.
Tost, H., Lawrence, M. G., Bruhl, C., Jockel, P., Team, G., and Team, S.-O.-D. A.: Uncertainties in atmospheric chemistry modelling due to convection parameterisations and subsequent scavenging, Atmos. Chem. Phys., 10, 1931–1951, https://doi.org/10.5194/acp-10-1931-2010, 2010.
Vernier, J.-P., Pommereau, J.-P., Thomason, L. W., Pelon, J., Garnier, A., Deshler, T., Jumelet, J., and Nielsen, J. K.: Overshooting of clean tropospheric air in the tropical lower stratosphere as seen by the CALIPSO lidar, Atmos. Chem. Phys., 11, 9683–9696, https://doi.org/10.5194/acp-11-9683-2011, 2011a.
Vernier, J.-P., Thomason, L. W., Pommereau, J. P., Bourassa, A., Pelon, J., Garnier, A., Hauchecorne, A., Blanot, L., Trepte, C., Degenstein, D., and Vargas, F.: Major influence of tropical volcanic eruptions on the stratospheric aerosol layer during the last decade, Geophys. Res. Lett., 38, L12807, https://doi.org/10.1029/2011GL047563, 2011b.
Wanninkhof, R.: Relationship between wind-speed and gas-exchange over the ocean, J. Geophys. Res.-Oceans., 97, 7373–7382, https://doi.org/10.1029/92jc00188, 1992.
Wofsy, S. C., Daube, B. C., Jimenez, R. Kort, E., Pittman, J. V, Park, S., Commane, R., Xiang, B., Santoni, G., Jacob, D., Fisher, J., Pickett-Heaps, C., Wang, H., Wecht, K., Wang, Q.-Q., Stephens, B. B., Shertz, S., Watt, A. S., Romashkin, P., Campos, T., Haggerty, J., Cooper, W. A., Rogers, D., Beaton, S., Hendershot, R., Elkins, J. W., Fahey, D. W., Gao, R. S., Moore, F., Montzka, S. A., Schwarz, J. P., Perring, A. E., Hurst, D., Miller, B. R., Sweeney, C., Oltmans, S., Nance, D., Hintsa, E., Dutton, G., Watts, L. A., Spackman, J. R., Rosenlof, K. H., Ray, E. A., Hall, B., Zondlo, M. A., Diao, M., Keeling, R., Bent, J., Atlas, E. L., Lueb, R., and Mahoney, M. J.: HIPPO combined discrete flask and GC sample GHG, halo-, hydrocarbon data (R_20121129), Carbon Dioxide Information Analysis Center, Oak Ridge National Laboratory, Oak Ridge, Tennessee, USA, available at: http://dx.doi.org/10.3334/CDIAC/hippo_012 (Release 20121129), 2012.
Zindler, C., Bracher, A., Marandino, C. A., Taylor, B., Torrecilla, E., Kock, A., and Bange, H. W.: Sulphur compounds, methane, and phytoplankton: interactions along a north-south transit in the western Pacific Ocean, Biogeosciences, 10, 3297–3311, https://doi.org/10.5194/bg-10-3297-2013, 2013.
Download
The requested paper has a corresponding corrigendum published. Please read the corrigendum first before downloading the article.
- Article
(1768 KB) - Metadata XML
Special issue
Altmetrics
Final-revised paper
Preprint