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IF 5.509
5.689CiteScore
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h5-index 86
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Volume 15, issue 14
Atmos. Chem. Phys., 15, 8201-8216, 2015
https://doi.org/10.5194/acp-15-8201-2015
© Author(s) 2015. This work is distributed under
the Creative Commons Attribution 3.0 License.
https://doi.org/10.5194/acp-15-8201-2015
© Author(s) 2015. This work is distributed under
the Creative Commons Attribution 3.0 License.
Atmos. Chem. Phys., 15, 8201-8216, 2015
https://doi.org/10.5194/acp-15-8201-2015
© Author(s) 2015. This work is distributed under
the Creative Commons Attribution 3.0 License.
https://doi.org/10.5194/acp-15-8201-2015
© Author(s) 2015. This work is distributed under
the Creative Commons Attribution 3.0 License.
Research article 24 Jul 2015
Research article | 24 Jul 2015
Climate responses to anthropogenic emissions of short-lived climate pollutants
L. H. Baker et al.Related authors
Ross Noel Bannister, Stefano Migliorini, Alison Clare Rudd, and Laura Hart Baker
Geosci. Model Dev. Discuss., https://doi.org/10.5194/gmd-2017-260, https://doi.org/10.5194/gmd-2017-260, 2017
Revised manuscript has not been submitted
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An ensemble of weather forecasts (i.e. multiple forecasts) contains useful information that a traditional single forecast does not have. Most existing forecast ensembles though have few members (ensemble too small), meaning that the information that they contain is noisy. This paper shows how more ensemble members can be generated from an existing (small) ensemble, and how the value added by the extra members can be assessed in a quantitative way.
Nicolas Bellouin, Laura Baker, Øivind Hodnebrog, Dirk Olivié, Ribu Cherian, Claire Macintosh, Bjørn Samset, Anna Esteve, Borgar Aamaas, Johannes Quaas, and Gunnar Myhre
Atmos. Chem. Phys., 16, 13885-13910, https://doi.org/10.5194/acp-16-13885-2016, https://doi.org/10.5194/acp-16-13885-2016, 2016
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This study uses global climate models to quantify how strongly man-made emissions of selected pollutants modify the energy budget of the Earth. The pollutants studied interact directly and indirectly with sunlight and terrestrial radiation and remain a relatively short time in the atmosphere, leading to regional and seasonal variations in their impacts. This new data set is useful to compare the potential climate impacts of different pollutants in support of policies to reduce climate change.
A. Stohl, B. Aamaas, M. Amann, L. H. Baker, N. Bellouin, T. K. Berntsen, O. Boucher, R. Cherian, W. Collins, N. Daskalakis, M. Dusinska, S. Eckhardt, J. S. Fuglestvedt, M. Harju, C. Heyes, Ø. Hodnebrog, J. Hao, U. Im, M. Kanakidou, Z. Klimont, K. Kupiainen, K. S. Law, M. T. Lund, R. Maas, C. R. MacIntosh, G. Myhre, S. Myriokefalitakis, D. Olivié, J. Quaas, B. Quennehen, J.-C. Raut, S. T. Rumbold, B. H. Samset, M. Schulz, Ø. Seland, K. P. Shine, R. B. Skeie, S. Wang, K. E. Yttri, and T. Zhu
Atmos. Chem. Phys., 15, 10529-10566, https://doi.org/10.5194/acp-15-10529-2015, https://doi.org/10.5194/acp-15-10529-2015, 2015
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This paper presents a summary of the findings of the ECLIPSE EU project. The project has investigated the climate and air quality impacts of short-lived climate pollutants (especially methane, ozone, aerosols) and has designed a global mitigation strategy that maximizes co-benefits between air quality and climate policy. Transient climate model simulations allowed quantifying the impacts on temperature (e.g., reduction in global warming by 0.22K for the decade 2041-2050) and precipitation.
L. H. Baker, A. C. Rudd, S. Migliorini, and R. N. Bannister
Nonlin. Processes Geophys., 21, 19-39, https://doi.org/10.5194/npg-21-19-2014, https://doi.org/10.5194/npg-21-19-2014, 2014
Edward Gryspeerdt, Tom Goren, Odran Sourdeval, Johannes Quaas, Johannes Mülmenstädt, Sudhakar Dipu, Claudia Unglaub, Andrew Gettelman, and Matthew Christensen
Atmos. Chem. Phys., 19, 5331-5347, https://doi.org/10.5194/acp-19-5331-2019, https://doi.org/10.5194/acp-19-5331-2019, 2019
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The liquid water path (LWP) is the strongest control on cloud albedo, such that a small change in LWP can have a large radiative impact. By changing the droplet number concentration (Nd) aerosols may be able to change the LWP, but the sign and magnitude of the effect is unclear. This work uses satellite data to investigate the relationship between Nd and LWP at a global scale and in response to large aerosol perturbations, suggesting that a strong decrease in LWP at high Nd may be overestimated.
Christoph Böhm, Odran Sourdeval, Johannes Mülmenstädt, Johannes Quaas, and Susanne Crewell
Atmos. Meas. Tech., 12, 1841-1860, https://doi.org/10.5194/amt-12-1841-2019, https://doi.org/10.5194/amt-12-1841-2019, 2019
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The cloud base height (CBH) is important for air traffic, for describing the energy budget of the Earth and for other applications. Ground-based CBH measurements are only available for individual sites and mostly limited to land. Satellites are a powerful tool for global coverage. While the cloud top height is derived operationally, the derivation of CBH from space is more difficult as the clouds hide their base. Here, we present a method to retrieve the CBH from multi-angle satellite data.
Øivind Hodnebrog, Gunnar Myhre, Bjørn H. Samset, Kari Alterskjær, Timothy Andrews, Olivier Boucher, Gregory Faluvegi, Dagmar Fläschner, Piers M. Forster, Matthew Kasoar, Alf Kirkevåg, Jean-Francois Lamarque, Dirk Olivié, Thomas B. Richardson, Dilshad Shawki, Drew Shindell, Keith P. Shine, Philip Stier, Toshihiko Takemura, Apostolos Voulgarakis, and Duncan Watson-Parris
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2019-121, https://doi.org/10.5194/acp-2019-121, 2019
Manuscript under review for ACP
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Different greenhouse gases (e.g. CO2) and aerosols (e.g. black carbon) impact the Earth’s water cycle differently. Here we investigate how various gases and particles impact atmospheric water vapour and its lifetime, i.e., the average number of days that water vapour stays in the atmosphere after evaporation and before precipitation. We find that this lifetime could increase by around 25 % near the end of this century, from a present-day value of 8 days, if we follow a business-as-usual pathway.
Jacob Schacht, Bernd Heinold, Johannes Quaas, John Backman, Ribu Cherian, Andre Ehrlich, Andreas Herber, Wan Ting Katty Huang, Yutaka Kondo, Andreas Massling, P. R. Sinha, Bernadett Weinzierl, Marco Zanatta, and Ina Tegen
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2019-71, https://doi.org/10.5194/acp-2019-71, 2019
Manuscript under review for ACP
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The Arctic is warming faster than the rest of Earth. Black carbon (BC) aerosol contributes to this Arctic Amplification by direct and indirect aerosol radiative effects while distributed in the air or deposited on snow and ice. The aerosol-climate model ECHAM-HAM is used to estimate the direct radiative effect (DRE). Airborne and near-surface BC measurements are used to evaluate the model and give an uncertainty range for the burden and DRE of Arctic BC caused by different emission inventories.
Hailing Jia, Xiaoyan Ma, Johannes Quaas, Yan Yin, and Tom Qiu
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2019-47, https://doi.org/10.5194/acp-2019-47, 2019
Manuscript under review for ACP
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We systematically assess how and to what extent the satellite retrieval biases may affect the correlations, as well as explore the underlying physical mechanisms. It is noted that the retrieval biases of both cloud and aerosol can result in a serious overestimation of the slope of CER-AI. The positive correlations more likely occur in case of drier cloud top and stronger turbulence in clouds, implying entrainment mixing might be a possible physical interpretation for such a positive CER-AI slope.
Johannes Mülmenstädt, Edward Gryspeerdt, Marc Salzmann, Po-Lun Ma, Sudhakar Dipu, and Johannes Quaas
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2018-1304, https://doi.org/10.5194/acp-2018-1304, 2019
Manuscript under review for ACP
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The effect of aerosol–cloud interactions (ACI) on the Earth's energy budget continues to be highly uncertain. We decompose the effective radiative forcing by ACI (ERFaci) into the instantaneous forcing due to anthropogenic increases in the number of cloud droplets and fast responses of clouds properties to the droplet number perturbation in the ECHAM-HAMMOZ aerosol–climate model. This decomposition maps onto the IPCC's Fifth Assessment Report analysis of ERFaci more directly than previous work.
Johannes Mülmenstädt, Odran Sourdeval, David S. Henderson, Tristan S. L'Ecuyer, Claudia Unglaub, Leonore Jungandreas, Christoph Böhm, Lynn M. Russell, and Johannes Quaas
Earth Syst. Sci. Data, 10, 2279-2293, https://doi.org/10.5194/essd-10-2279-2018, https://doi.org/10.5194/essd-10-2279-2018, 2018
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One of the key pieces of information about a cloud is how high its base is. Unlike cloud top, cloud base is hard to observe from a satellite perspective – the cloud blocks the view. But without using satellites, it is difficult to compile global datasets. Here we describe how we worked around the limitations of a cloud-detecting laser satellite to observe global cloud base heights. This dataset will expand our knowledge of the cloudy atmosphere and its interaction with the planetary surface.
Marianne Tronstad Lund, Gunnar Myhre, Amund Søvde Haslerud, Ragnhild Bieltvedt Skeie, Jan Griesfeller, Stephen Matthew Platt, Rajesh Kumar, Cathrine Lund Myhre, and Michael Schulz
Geosci. Model Dev., 11, 4909-4931, https://doi.org/10.5194/gmd-11-4909-2018, https://doi.org/10.5194/gmd-11-4909-2018, 2018
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Atmospheric aerosols play a key role in the climate system, but their exact impact on the energy balance remains uncertain. Accurate representation of the geographical distribution and properties of aerosols in global models is key to reduce this uncertainty. Here we use a new emission inventory and a range of observations to carefully validate a state-of-the-art model and present an updated estimate of the net direct effect of anthropogenic aerosols since the preindustrial era.
Christoph Heinze, Veronika Eyring, Pierre Friedlingstein, Colin Jones, Yves Balkanski, Williams Collins, Thierry Fichefet, Shuang Gao, Alex Hall, Detelina Ivanova, Wolfgang Knorr, Reto Knutti, Alexander Löw, Michael Ponater, Martin G. Schultz, Michael Schulz, Pier Siebesma, Joao Teixeira, George Tselioudis, and Martin Vancoppenolle
Earth Syst. Dynam. Discuss., https://doi.org/10.5194/esd-2018-84, https://doi.org/10.5194/esd-2018-84, 2018
Revised manuscript under review for ESD
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We present an overview of climate feedbacks for Earth system components currently included in state-of-the-art Earth system models (ESMs) and discuss the challenges to evaluate and quantify them. The target group for this article includes generalists with a background in natural sciences and an interest in climate change as well as experts working in interdisciplinary climate research.
Jan Kretzschmar, Marc Salzmann, Johannes Mülmenstädt, and Johannes Quaas
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2018-1135, https://doi.org/10.5194/acp-2018-1135, 2018
Revised manuscript under review for ACP
Arlene M. Fiore, Emily V. Fischer, George P. Milly, Shubha Pandey Deolal, Oliver Wild, Daniel A. Jaffe, Johannes Staehelin, Olivia E. Clifton, Dan Bergmann, William Collins, Frank Dentener, Ruth M. Doherty, Bryan N. Duncan, Bernd Fischer, Stefan Gilge, Peter G. Hess, Larry W. Horowitz, Alexandru Lupu, Ian A. MacKenzie, Rokjin Park, Ludwig Ries, Michael G. Sanderson, Martin G. Schultz, Drew T. Shindell, Martin Steinbacher, David S. Stevenson, Sophie Szopa, Christoph Zellweger, and Guang Zeng
Atmos. Chem. Phys., 18, 15345-15361, https://doi.org/10.5194/acp-18-15345-2018, https://doi.org/10.5194/acp-18-15345-2018, 2018
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We demonstrate a proof-of-concept approach for applying northern midlatitude mountaintop peroxy acetyl nitrate (PAN) measurements and a multi-model ensemble during April to constrain the influence of continental-scale anthropogenic precursor emissions on PAN. Our findings imply a role for carefully coordinated multi-model ensembles in helping identify observations for discriminating among widely varying (and poorly constrained) model responses of atmospheric constituents to changes in emissions.
Odran Sourdeval, Edward Gryspeerdt, Martina Krämer, Tom Goren, Julien Delanoë, Armin Afchine, Friederike Hemmer, and Johannes Quaas
Atmos. Chem. Phys., 18, 14327-14350, https://doi.org/10.5194/acp-18-14327-2018, https://doi.org/10.5194/acp-18-14327-2018, 2018
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The number concentration of ice crystals (Ni) is a key cloud property that remains very uncertain due to difficulties in determining it using satellites. This lack of global observational constraints limits our ability to constrain this property in models responsible for predicting future climate. This pair of papers fills this gap by showing and analyzing the first rigorously evaluated global climatology of Ni, leading to new information shedding light on the processes that control high clouds.
Ragnhild Bieltvedt Skeie, Terje Berntsen, Magne Aldrin, Marit Holden, and Gunnar Myhre
Earth Syst. Dynam., 9, 879-894, https://doi.org/10.5194/esd-9-879-2018, https://doi.org/10.5194/esd-9-879-2018, 2018
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A key question in climate science is how the global mean surface temperature responds to changes in greenhouse gases. This dependency is quantified by the climate sensitivity, which is determined by the complex feedbacks in the climate system. In this study observations of past climate change are used to estimate this sensitivity. Our estimate is consistent with values for the equilibrium climate sensitivity estimated by complex climate models but sensitive to the use of uncertain input data.
Paul Petersik, Marc Salzmann, Jan Kretzschmar, Ribu Cherian, Daniel Mewes, and Johannes Quaas
Atmos. Chem. Phys., 18, 8589-8599, https://doi.org/10.5194/acp-18-8589-2018, https://doi.org/10.5194/acp-18-8589-2018, 2018
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Our study presents the first estimate of RFari using a global atmospheric model with a parameterization for subgrid-scale variability in RH that is consistent with the assumptions in the model. We find that the revision has a strong influence on the simulated radiative forcing (~ 31 %). In addition, we examine its effects on optical properties of the atmosphere and find an increase in AOD by about 7.8 %.
Tao Tang, Drew Shindell, Bjørn H. Samset, Oliviér Boucher, Piers M. Forster, Øivind Hodnebrog, Gunnar Myhre, Jana Sillmann, Apostolos Voulgarakis, Timothy Andrews, Gregory Faluvegi, Dagmar Fläschner, Trond Iversen, Matthew Kasoar, Viatcheslav Kharin, Alf Kirkevåg, Jean-Francois Lamarque, Dirk Olivié, Thomas Richardson, Camilla W. Stjern, and Toshihiko Takemura
Atmos. Chem. Phys., 18, 8439-8452, https://doi.org/10.5194/acp-18-8439-2018, https://doi.org/10.5194/acp-18-8439-2018, 2018
Edward Gryspeerdt, Johannes Quaas, Tom Goren, Daniel Klocke, and Matthias Brueck
Atmos. Chem. Phys., 18, 6157-6169, https://doi.org/10.5194/acp-18-6157-2018, https://doi.org/10.5194/acp-18-6157-2018, 2018
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Cirrus clouds can form by a variety of mechanisms, such as orographic uplift, through convective systems or through large-scale rising motions. In this work, an automated classification of cirrus clouds based on satellite and reanalysis data is presented to separate cirrus by these different formation mechanisms. The classification provides information on the ice origin and cloud-scale updraughts that could not be determined using satellite or reanalysis data alone.
Sunil Vadakkepuliyambatta, Ragnhild B. Skeie, Gunnar Myhre, Stig B. Dalsøren, Anna Silyakova, Norbert Schmidbauer, Cathrine Lund Myhre, and Jürgen Mienert
Earth Syst. Dynam. Discuss., https://doi.org/10.5194/esd-2017-110, https://doi.org/10.5194/esd-2017-110, 2017
Publication in ESD not foreseen
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Release of methane, one of the major greenhouse gases, from melting hydrates has been proposed as a mechanism that accelerated global warming in the past. We focus on Arctic Ocean warming as a robust case study for accelerated melting of hydrates, assessing the impact of Arctic methane release on global air temperatures during the next century. Contrary to popular belief, it is shown that methane emissions from melting hydrates from the Arctic seafloor is not a major driver of global warming.
Ross Noel Bannister, Stefano Migliorini, Alison Clare Rudd, and Laura Hart Baker
Geosci. Model Dev. Discuss., https://doi.org/10.5194/gmd-2017-260, https://doi.org/10.5194/gmd-2017-260, 2017
Revised manuscript has not been submitted
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An ensemble of weather forecasts (i.e. multiple forecasts) contains useful information that a traditional single forecast does not have. Most existing forecast ensembles though have few members (ensemble too small), meaning that the information that they contain is noisy. This paper shows how more ensemble members can be generated from an existing (small) ensemble, and how the value added by the extra members can be assessed in a quantitative way.
Huisheng Bian, Mian Chin, Didier A. Hauglustaine, Michael Schulz, Gunnar Myhre, Susanne E. Bauer, Marianne T. Lund, Vlassis A. Karydis, Tom L. Kucsera, Xiaohua Pan, Andrea Pozzer, Ragnhild B. Skeie, Stephen D. Steenrod, Kengo Sudo, Kostas Tsigaridis, Alexandra P. Tsimpidi, and Svetlana G. Tsyro
Atmos. Chem. Phys., 17, 12911-12940, https://doi.org/10.5194/acp-17-12911-2017, https://doi.org/10.5194/acp-17-12911-2017, 2017
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Atmospheric nitrate contributes notably to total aerosol mass in the present day and is likely to be more important over the next century, with a projected decline in SO2 and NOx emissions and increase in NH3 emissions. This paper investigates atmospheric nitrate using multiple global models and measurements. The study is part of the AeroCom phase III activity. The study is the first attempt to look at global atmospheric nitrate simulation at physical and chemical process levels.
Maria Sand, Bjørn H. Samset, Yves Balkanski, Susanne Bauer, Nicolas Bellouin, Terje K. Berntsen, Huisheng Bian, Mian Chin, Thomas Diehl, Richard Easter, Steven J. Ghan, Trond Iversen, Alf Kirkevåg, Jean-François Lamarque, Guangxing Lin, Xiaohong Liu, Gan Luo, Gunnar Myhre, Twan van Noije, Joyce E. Penner, Michael Schulz, Øyvind Seland, Ragnhild B. Skeie, Philip Stier, Toshihiko Takemura, Kostas Tsigaridis, Fangqun Yu, Kai Zhang, and Hua Zhang
Atmos. Chem. Phys., 17, 12197-12218, https://doi.org/10.5194/acp-17-12197-2017, https://doi.org/10.5194/acp-17-12197-2017, 2017
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The role of aerosols in the changing polar climate is not well understood and the aerosols are poorly constrained in the models. In this study we have compared output from 16 different aerosol models with available observations at both poles. We show that the model median is representative of the observations, but the model spread is large. The Arctic direct aerosol radiative effect over the industrial area is positive during spring due to black carbon and negative during summer due to sulfate.
Borgar Aamaas, Terje K. Berntsen, Jan S. Fuglestvedt, Keith P. Shine, and William J. Collins
Atmos. Chem. Phys., 17, 10795-10809, https://doi.org/10.5194/acp-17-10795-2017, https://doi.org/10.5194/acp-17-10795-2017, 2017
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The climate impacts for emissions of different pollutants can be made comparable with weighting factors. This article estimates these weights based on temperature change for short-lived pollutants, such as methane and black carbon. Emissions from different seasons and regions are compared, for instance Europe and East Asia. The responses are calculated for four regions, where we see that the responses can be much higher in the Arctic than globally in some cases.
Chris Huntingford, Hui Yang, Anna Harper, Peter M. Cox, Nicola Gedney, Eleanor J. Burke, Jason A. Lowe, Garry Hayman, William J. Collins, Stephen M. Smith, and Edward Comyn-Platt
Earth Syst. Dynam., 8, 617-626, https://doi.org/10.5194/esd-8-617-2017, https://doi.org/10.5194/esd-8-617-2017, 2017
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Recent UNFCCC climate meetings have placed much emphasis on constraining global warming to remain below 2 °C. The 2015 Paris meeting went further and gave an aspiration to fulfil a 1.5 °C threshold. We provide a flexible set of algebraic global temperature profiles that stabilise to either target. This will potentially allow the climate research community to estimate local climatic implications for these temperature profiles, along with emissions trajectories to fulfil them.
Sudhakar Dipu, Johannes Quaas, Ralf Wolke, Jens Stoll, Andreas Mühlbauer, Odran Sourdeval, Marc Salzmann, Bernd Heinold, and Ina Tegen
Geosci. Model Dev., 10, 2231-2246, https://doi.org/10.5194/gmd-10-2231-2017, https://doi.org/10.5194/gmd-10-2231-2017, 2017
Thomas Gasser, Glen P. Peters, Jan S. Fuglestvedt, William J. Collins, Drew T. Shindell, and Philippe Ciais
Earth Syst. Dynam., 8, 235-253, https://doi.org/10.5194/esd-8-235-2017, https://doi.org/10.5194/esd-8-235-2017, 2017
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Emission metrics such as GWP or GTP are used to put non-CO2 species on a
CO2-equivalentscale. In the fifth IPCC report the metrics are inconsistent, as the climate–carbon feedback is included only for CO2 but not for non-CO2 species. Here, we simulate a new impulse response function for the feedback, and we use it to correct the metrics. For instance, 1 g of CH4 is equivalent to 31 g of CO2 (instead of 28 g) following the corrected GWP100 metric. It is 34 g if other factors are also updated.
Gunnar Myhre, Wenche Aas, Ribu Cherian, William Collins, Greg Faluvegi, Mark Flanner, Piers Forster, Øivind Hodnebrog, Zbigniew Klimont, Marianne T. Lund, Johannes Mülmenstädt, Cathrine Lund Myhre, Dirk Olivié, Michael Prather, Johannes Quaas, Bjørn H. Samset, Jordan L. Schnell, Michael Schulz, Drew Shindell, Ragnhild B. Skeie, Toshihiko Takemura, and Svetlana Tsyro
Atmos. Chem. Phys., 17, 2709-2720, https://doi.org/10.5194/acp-17-2709-2017, https://doi.org/10.5194/acp-17-2709-2017, 2017
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Over the past decades, the geographical distribution of emissions of substances that alter the atmospheric energy balance has changed due to economic growth and pollution regulations. Here, we show the resulting changes to aerosol and ozone abundances and their radiative forcing using recently updated emission data for the period 1990–2015, as simulated by seven global atmospheric composition models. The global mean radiative forcing is more strongly positive than reported in IPCC AR5.
William J. Collins, Jean-François Lamarque, Michael Schulz, Olivier Boucher, Veronika Eyring, Michaela I. Hegglin, Amanda Maycock, Gunnar Myhre, Michael Prather, Drew Shindell, and Steven J. Smith
Geosci. Model Dev., 10, 585-607, https://doi.org/10.5194/gmd-10-585-2017, https://doi.org/10.5194/gmd-10-585-2017, 2017
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We have designed a set of climate model experiments called the Aerosol Chemistry Model Intercomparison Project (AerChemMIP). These are designed to quantify the climate and air quality impacts of aerosols and chemically reactive gases in the climate models that are used to simulate past and future climate. We hope that many climate modelling centres will choose to run these experiments to help understand the contribution of aerosols and chemistry to climate change.
Christopher P. Webber, Helen F. Dacre, William J. Collins, and Giacomo Masato
Atmos. Chem. Phys., 17, 867-881, https://doi.org/10.5194/acp-17-867-2017, https://doi.org/10.5194/acp-17-867-2017, 2017
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The influence of synoptic meteorology on UK PM10 concentration ([PM110]) is analysed. ERA-Interim reanalysis data are used to detect upper-tropospheric wave breaking that explains much of the UK winter synoptic meteorological variability. Wave breaking is shown to positively impact UK [PM10], with a persistent Ω block feature resulting in the greatest probability of exceeding a hazardous UK [PM10]. The meteorological dynamics of UK PM10 exceedances are better understood following this study.
Massimo Cassiani, Andreas Stohl, Dirk Olivié, Øyvind Seland, Ingo Bethke, Ignacio Pisso, and Trond Iversen
Geosci. Model Dev., 9, 4029-4048, https://doi.org/10.5194/gmd-9-4029-2016, https://doi.org/10.5194/gmd-9-4029-2016, 2016
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FLEXPART is a community model used by many scientists. Here, an alternative FLEXPART model version has been developed, tailored to use with the output data generated by the Norwegian Earth System Model (NorESM1-M). The model provides an advanced tool to analyse and diagnose atmospheric transport properties of the climate model NorESM. To validate the model, several tests were performed that offered the possibility to investigate some aspects of offline global dispersion modelling.
Nicolas Bellouin, Laura Baker, Øivind Hodnebrog, Dirk Olivié, Ribu Cherian, Claire Macintosh, Bjørn Samset, Anna Esteve, Borgar Aamaas, Johannes Quaas, and Gunnar Myhre
Atmos. Chem. Phys., 16, 13885-13910, https://doi.org/10.5194/acp-16-13885-2016, https://doi.org/10.5194/acp-16-13885-2016, 2016
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This study uses global climate models to quantify how strongly man-made emissions of selected pollutants modify the energy budget of the Earth. The pollutants studied interact directly and indirectly with sunlight and terrestrial radiation and remain a relatively short time in the atmosphere, leading to regional and seasonal variations in their impacts. This new data set is useful to compare the potential climate impacts of different pollutants in support of policies to reduce climate change.
Camilla Weum Stjern, Bjørn Hallvard Samset, Gunnar Myhre, Huisheng Bian, Mian Chin, Yanko Davila, Frank Dentener, Louisa Emmons, Johannes Flemming, Amund Søvde Haslerud, Daven Henze, Jan Eiof Jonson, Tom Kucsera, Marianne Tronstad Lund, Michael Schulz, Kengo Sudo, Toshihiko Takemura, and Simone Tilmes
Atmos. Chem. Phys., 16, 13579-13599, https://doi.org/10.5194/acp-16-13579-2016, https://doi.org/10.5194/acp-16-13579-2016, 2016
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Air pollution can reach distant regions through intercontinental transport. Here we first present results from the Hemispheric Transport of Air Pollution Phase 2 exercise, where many models performed the same set of coordinated emission-reduction experiments. We find that mitigations have considerable extra-regional effects, and show that this is particularly true for black carbon emissions, as long-range transport elevates aerosols to higher levels where their radiative influence is stronger.
B. Quennehen, J.-C. Raut, K. S. Law, N. Daskalakis, G. Ancellet, C. Clerbaux, S.-W. Kim, M. T. Lund, G. Myhre, D. J. L. Olivié, S. Safieddine, R. B. Skeie, J. L. Thomas, S. Tsyro, A. Bazureau, N. Bellouin, M. Hu, M. Kanakidou, Z. Klimont, K. Kupiainen, S. Myriokefalitakis, J. Quaas, S. T. Rumbold, M. Schulz, R. Cherian, A. Shimizu, J. Wang, S.-C. Yoon, and T. Zhu
Atmos. Chem. Phys., 16, 10765-10792, https://doi.org/10.5194/acp-16-10765-2016, https://doi.org/10.5194/acp-16-10765-2016, 2016
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This paper evaluates the ability of six global models and one regional model in reproducing short-lived pollutants (defined here as ozone and its precursors, aerosols and black carbon) concentrations over Asia using satellite, ground-based and airborne observations.
Key findings are that models homogeneously reproduce the trace gas observations although nitrous oxides are underestimated, whereas the aerosol distributions are heterogeneously reproduced, implicating important uncertainties.
Raquel A. Silva, J. Jason West, Jean-François Lamarque, Drew T. Shindell, William J. Collins, Stig Dalsoren, Greg Faluvegi, Gerd Folberth, Larry W. Horowitz, Tatsuya Nagashima, Vaishali Naik, Steven T. Rumbold, Kengo Sudo, Toshihiko Takemura, Daniel Bergmann, Philip Cameron-Smith, Irene Cionni, Ruth M. Doherty, Veronika Eyring, Beatrice Josse, Ian A. MacKenzie, David Plummer, Mattia Righi, David S. Stevenson, Sarah Strode, Sophie Szopa, and Guang Zengast
Atmos. Chem. Phys., 16, 9847-9862, https://doi.org/10.5194/acp-16-9847-2016, https://doi.org/10.5194/acp-16-9847-2016, 2016
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Using ozone and PM2.5 concentrations from the ACCMIP ensemble of chemistry-climate models for the four Representative Concentration Pathway scenarios (RCPs), together with projections of future population and baseline mortality rates, we quantify the human premature mortality impacts of future ambient air pollution in 2030, 2050 and 2100, relative to 2000 concentrations. We also estimate the global mortality burden of ozone and PM2.5 in 2000 and each future period.
Matthew Kasoar, Apostolos Voulgarakis, Jean-François Lamarque, Drew T. Shindell, Nicolas Bellouin, William J. Collins, Greg Faluvegi, and Kostas Tsigaridis
Atmos. Chem. Phys., 16, 9785-9804, https://doi.org/10.5194/acp-16-9785-2016, https://doi.org/10.5194/acp-16-9785-2016, 2016
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Computer models are our primary tool to investigate how fossil-fuel emissions are affecting the climate. Here, we used three different climate models to see how they simulate the response to removing sulfur dioxide emissions from China. We found that the models disagreed substantially on how large the climate effect is from the emissions in this region. This range of outcomes is concerning if scientists or policy makers have to rely on any one model when performing their own studies.
N. I. Kristiansen, A. Stohl, D. J. L. Olivié, B. Croft, O. A. Søvde, H. Klein, T. Christoudias, D. Kunkel, S. J. Leadbetter, Y. H. Lee, K. Zhang, K. Tsigaridis, T. Bergman, N. Evangeliou, H. Wang, P.-L. Ma, R. C. Easter, P. J. Rasch, X. Liu, G. Pitari, G. Di Genova, S. Y. Zhao, Y. Balkanski, S. E. Bauer, G. S. Faluvegi, H. Kokkola, R. V. Martin, J. R. Pierce, M. Schulz, D. Shindell, H. Tost, and H. Zhang
Atmos. Chem. Phys., 16, 3525-3561, https://doi.org/10.5194/acp-16-3525-2016, https://doi.org/10.5194/acp-16-3525-2016, 2016
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Processes affecting aerosol removal from the atmosphere are not fully understood. In this study we investigate to what extent atmospheric transport models can reproduce observed loss of aerosols. We compare measurements of radioactive isotopes, that attached to ambient sulfate aerosols during the 2011 Fukushima nuclear accident, to 19 models using identical emissions. Results indicate aerosol removal that is too fast in most models, and apply to aerosols that have undergone long-range transport.
Stig B. Dalsøren, Cathrine L. Myhre, Gunnar Myhre, Angel J. Gomez-Pelaez, Ole A. Søvde, Ivar S. A. Isaksen, Ray F. Weiss, and Christina M. Harth
Atmos. Chem. Phys., 16, 3099-3126, https://doi.org/10.5194/acp-16-3099-2016, https://doi.org/10.5194/acp-16-3099-2016, 2016
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Methane is a key greenhouse gas. Observations at surface sites show a more than 10 % increase over the period 1984–2012. Using an atmospheric model we calculate a growth in the atmospheric chemical methane loss the last decades. Without this, the rise in atmospheric methane would have been even higher. The model reproduces trends and short-term variations in observation data. However, some discrepancies in model performance question the accuracy in estimates of emission increases in Asia.
A. Stohl, B. Aamaas, M. Amann, L. H. Baker, N. Bellouin, T. K. Berntsen, O. Boucher, R. Cherian, W. Collins, N. Daskalakis, M. Dusinska, S. Eckhardt, J. S. Fuglestvedt, M. Harju, C. Heyes, Ø. Hodnebrog, J. Hao, U. Im, M. Kanakidou, Z. Klimont, K. Kupiainen, K. S. Law, M. T. Lund, R. Maas, C. R. MacIntosh, G. Myhre, S. Myriokefalitakis, D. Olivié, J. Quaas, B. Quennehen, J.-C. Raut, S. T. Rumbold, B. H. Samset, M. Schulz, Ø. Seland, K. P. Shine, R. B. Skeie, S. Wang, K. E. Yttri, and T. Zhu
Atmos. Chem. Phys., 15, 10529-10566, https://doi.org/10.5194/acp-15-10529-2015, https://doi.org/10.5194/acp-15-10529-2015, 2015
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This paper presents a summary of the findings of the ECLIPSE EU project. The project has investigated the climate and air quality impacts of short-lived climate pollutants (especially methane, ozone, aerosols) and has designed a global mitigation strategy that maximizes co-benefits between air quality and climate policy. Transient climate model simulations allowed quantifying the impacts on temperature (e.g., reduction in global warming by 0.22K for the decade 2041-2050) and precipitation.
K. P. Shine, R. P. Allan, W. J. Collins, and J. S. Fuglestvedt
Earth Syst. Dynam., 6, 525-540, https://doi.org/10.5194/esd-6-525-2015, https://doi.org/10.5194/esd-6-525-2015, 2015
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Emissions due to human activity impact on rainfall. This impact depends on the properties of the gases or particles that are emitted. This paper uses improved understanding of relevant processes to produce a new measure, called the Global Precipitation-change Potential, which allows a direct comparison of the effect of different emissions on global-mean rainfall. Carbon dioxide, in the years following its emission, is shown to be less effective than methane emissions at causing rainfall change.
V. N. Aswathy, O. Boucher, M. Quaas, U. Niemeier, H. Muri, J. Mülmenstädt, and J. Quaas
Atmos. Chem. Phys., 15, 9593-9610, https://doi.org/10.5194/acp-15-9593-2015, https://doi.org/10.5194/acp-15-9593-2015, 2015
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Simulations conducted in the GeoMIP and IMPLICC model intercomparison studies for climate engineering by stratospheric sulfate injection and marine cloud brightening via sea salt are analysed and compared to the reference scenario RCP4.5. The focus is on extremes in surface temperature and precipitation. It is found that the extreme changes mostly follow the mean changes and that extremes are also in general well mitigated, except for in polar regions.
S. Eckhardt, B. Quennehen, D. J. L. Olivié, T. K. Berntsen, R. Cherian, J. H. Christensen, W. Collins, S. Crepinsek, N. Daskalakis, M. Flanner, A. Herber, C. Heyes, Ø. Hodnebrog, L. Huang, M. Kanakidou, Z. Klimont, J. Langner, K. S. Law, M. T. Lund, R. Mahmood, A. Massling, S. Myriokefalitakis, I. E. Nielsen, J. K. Nøjgaard, J. Quaas, P. K. Quinn, J.-C. Raut, S. T. Rumbold, M. Schulz, S. Sharma, R. B. Skeie, H. Skov, T. Uttal, K. von Salzen, and A. Stohl
Atmos. Chem. Phys., 15, 9413-9433, https://doi.org/10.5194/acp-15-9413-2015, https://doi.org/10.5194/acp-15-9413-2015, 2015
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The concentrations of sulfate, black carbon and other aerosols in the Arctic are characterized by high values in late winter and spring (so-called Arctic Haze) and low values in summer. Models have long been struggling to capture this seasonality. In this study, we evaluate sulfate and BC concentrations from different updated models and emissions against a comprehensive pan-Arctic measurement data set. We find that the models improved but still struggle to get the maximum concentrations.
R. M. Bright, G. Myhre, R. Astrup, C. Antón-Fernández, and A. H. Strømman
Biogeosciences, 12, 2195-2205, https://doi.org/10.5194/bg-12-2195-2015, https://doi.org/10.5194/bg-12-2195-2015, 2015
G. Myhre and B. H. Samset
Atmos. Chem. Phys., 15, 2883-2888, https://doi.org/10.5194/acp-15-2883-2015, https://doi.org/10.5194/acp-15-2883-2015, 2015
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Radiative forcing (RF) of black carbon (BC) in the atmosphere is estimated using radiative transfer codes of various complexities. Here we show that the two-stream radiative transfer codes used most in climate models give overly strong forward scattering, leading to enhanced absorption at the surface and overly weak absorption by BC. Such calculations are found to underestimate RF in all sky conditions by 10% for global mean, relative to the more sophisticated multi-stream model.
B. H. Samset, G. Myhre, A. Herber, Y. Kondo, S.-M. Li, N. Moteki, M. Koike, N. Oshima, J. P. Schwarz, Y. Balkanski, S. E. Bauer, N. Bellouin, T. K. Berntsen, H. Bian, M. Chin, T. Diehl, R. C. Easter, S. J. Ghan, T. Iversen, A. Kirkevåg, J.-F. Lamarque, G. Lin, X. Liu, J. E. Penner, M. Schulz, Ø. Seland, R. B. Skeie, P. Stier, T. Takemura, K. Tsigaridis, and K. Zhang
Atmos. Chem. Phys., 14, 12465-12477, https://doi.org/10.5194/acp-14-12465-2014, https://doi.org/10.5194/acp-14-12465-2014, 2014
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Far from black carbon (BC) emission sources, present climate models are unable to reproduce flight measurements. By comparing recent models with data, we find that the atmospheric lifetime of BC may be overestimated in models. By adjusting modeled BC concentrations to measurements in remote regions - over oceans and at high altitudes - we arrive at a reduced estimate for BC radiative forcing over the industrial era.
S. Archer-Nicholls, D. Lowe, S. Utembe, J. Allan, R. A. Zaveri, J. D. Fast, Ø. Hodnebrog, H. Denier van der Gon, and G. McFiggans
Geosci. Model Dev., 7, 2557-2579, https://doi.org/10.5194/gmd-7-2557-2014, https://doi.org/10.5194/gmd-7-2557-2014, 2014
K. Tsigaridis, N. Daskalakis, M. Kanakidou, P. J. Adams, P. Artaxo, R. Bahadur, Y. Balkanski, S. E. Bauer, N. Bellouin, A. Benedetti, T. Bergman, T. K. Berntsen, J. P. Beukes, H. Bian, K. S. Carslaw, M. Chin, G. Curci, T. Diehl, R. C. Easter, S. J. Ghan, S. L. Gong, A. Hodzic, C. R. Hoyle, T. Iversen, S. Jathar, J. L. Jimenez, J. W. Kaiser, A. Kirkevåg, D. Koch, H. Kokkola, Y. H Lee, G. Lin, X. Liu, G. Luo, X. Ma, G. W. Mann, N. Mihalopoulos, J.-J. Morcrette, J.-F. Müller, G. Myhre, S. Myriokefalitakis, N. L. Ng, D. O'Donnell, J. E. Penner, L. Pozzoli, K. J. Pringle, L. M. Russell, M. Schulz, J. Sciare, Ø. Seland, D. T. Shindell, S. Sillman, R. B. Skeie, D. Spracklen, T. Stavrakou, S. D. Steenrod, T. Takemura, P. Tiitta, S. Tilmes, H. Tost, T. van Noije, P. G. van Zyl, K. von Salzen, F. Yu, Z. Wang, Z. Wang, R. A. Zaveri, H. Zhang, K. Zhang, Q. Zhang, and X. Zhang
Atmos. Chem. Phys., 14, 10845-10895, https://doi.org/10.5194/acp-14-10845-2014, https://doi.org/10.5194/acp-14-10845-2014, 2014
J. Huttunen, A. Arola, G. Myhre, A. V. Lindfors, T. Mielonen, S. Mikkonen, J. S. Schafer, S. N. Tripathi, M. Wild, M. Komppula, and K. E. J. Lehtinen
Atmos. Chem. Phys., 14, 6103-6110, https://doi.org/10.5194/acp-14-6103-2014, https://doi.org/10.5194/acp-14-6103-2014, 2014
R. B. Skeie, T. Berntsen, M. Aldrin, M. Holden, and G. Myhre
Earth Syst. Dynam., 5, 139-175, https://doi.org/10.5194/esd-5-139-2014, https://doi.org/10.5194/esd-5-139-2014, 2014
F. M. O'Connor, C. E. Johnson, O. Morgenstern, N. L. Abraham, P. Braesicke, M. Dalvi, G. A. Folberth, M. G. Sanderson, P. J. Telford, A. Voulgarakis, P. J. Young, G. Zeng, W. J. Collins, and J. A. Pyle
Geosci. Model Dev., 7, 41-91, https://doi.org/10.5194/gmd-7-41-2014, https://doi.org/10.5194/gmd-7-41-2014, 2014
L. H. Baker, A. C. Rudd, S. Migliorini, and R. N. Bannister
Nonlin. Processes Geophys., 21, 19-39, https://doi.org/10.5194/npg-21-19-2014, https://doi.org/10.5194/npg-21-19-2014, 2014
A. Arola, T. F. Eck, J. Huttunen, K. E. J. Lehtinen, A. V. Lindfors, G. Myhre, A. Smirnov, S. N. Tripathi, and H. Yu
Atmos. Chem. Phys., 13, 7895-7901, https://doi.org/10.5194/acp-13-7895-2013, https://doi.org/10.5194/acp-13-7895-2013, 2013
M. M. Fry, M. D. Schwarzkopf, Z. Adelman, V. Naik, W. J. Collins, and J. J. West
Atmos. Chem. Phys., 13, 5381-5399, https://doi.org/10.5194/acp-13-5381-2013, https://doi.org/10.5194/acp-13-5381-2013, 2013
V. Naik, A. Voulgarakis, A. M. Fiore, L. W. Horowitz, J.-F. Lamarque, M. Lin, M. J. Prather, P. J. Young, D. Bergmann, P. J. Cameron-Smith, I. Cionni, W. J. Collins, S. B. Dalsøren, R. Doherty, V. Eyring, G. Faluvegi, G. A. Folberth, B. Josse, Y. H. Lee, I. A. MacKenzie, T. Nagashima, T. P. C. van Noije, D. A. Plummer, M. Righi, S. T. Rumbold, R. Skeie, D. T. Shindell, D. S. Stevenson, S. Strode, K. Sudo, S. Szopa, and G. Zeng
Atmos. Chem. Phys., 13, 5277-5298, https://doi.org/10.5194/acp-13-5277-2013, https://doi.org/10.5194/acp-13-5277-2013, 2013
K. W. Bowman, D. T. Shindell, H. M. Worden, J.F. Lamarque, P. J. Young, D. S. Stevenson, Z. Qu, M. de la Torre, D. Bergmann, P. J. Cameron-Smith, W. J. Collins, R. Doherty, S. B. Dalsøren, G. Faluvegi, G. Folberth, L. W. Horowitz, B. M. Josse, Y. H. Lee, I. A. MacKenzie, G. Myhre, T. Nagashima, V. Naik, D. A. Plummer, S. T. Rumbold, R. B. Skeie, S. A. Strode, K. Sudo, S. Szopa, A. Voulgarakis, G. Zeng, S. S. Kulawik, A. M. Aghedo, and J. R. Worden
Atmos. Chem. Phys., 13, 4057-4072, https://doi.org/10.5194/acp-13-4057-2013, https://doi.org/10.5194/acp-13-4057-2013, 2013
M. S. Eide, S. B. Dalsøren, Ø. Endresen, B. Samset, G. Myhre, J. Fuglestvedt, and T. Berntsen
Atmos. Chem. Phys., 13, 4183-4201, https://doi.org/10.5194/acp-13-4183-2013, https://doi.org/10.5194/acp-13-4183-2013, 2013
P. Stier, N. A. J. Schutgens, N. Bellouin, H. Bian, O. Boucher, M. Chin, S. Ghan, N. Huneeus, S. Kinne, G. Lin, X. Ma, G. Myhre, J. E. Penner, C. A. Randles, B. Samset, M. Schulz, T. Takemura, F. Yu, H. Yu, and C. Zhou
Atmos. Chem. Phys., 13, 3245-3270, https://doi.org/10.5194/acp-13-3245-2013, https://doi.org/10.5194/acp-13-3245-2013, 2013
D. T. Shindell, J.-F. Lamarque, M. Schulz, M. Flanner, C. Jiao, M. Chin, P. J. Young, Y. H. Lee, L. Rotstayn, N. Mahowald, G. Milly, G. Faluvegi, Y. Balkanski, W. J. Collins, A. J. Conley, S. Dalsoren, R. Easter, S. Ghan, L. Horowitz, X. Liu, G. Myhre, T. Nagashima, V. Naik, S. T. Rumbold, R. Skeie, K. Sudo, S. Szopa, T. Takemura, A. Voulgarakis, J.-H. Yoon, and F. Lo
Atmos. Chem. Phys., 13, 2939-2974, https://doi.org/10.5194/acp-13-2939-2013, https://doi.org/10.5194/acp-13-2939-2013, 2013
D. S. Stevenson, P. J. Young, V. Naik, J.-F. Lamarque, D. T. Shindell, A. Voulgarakis, R. B. Skeie, S. B. Dalsoren, G. Myhre, T. K. Berntsen, G. A. Folberth, S. T. Rumbold, W. J. Collins, I. A. MacKenzie, R. M. Doherty, G. Zeng, T. P. C. van Noije, A. Strunk, D. Bergmann, P. Cameron-Smith, D. A. Plummer, S. A. Strode, L. Horowitz, Y. H. Lee, S. Szopa, K. Sudo, T. Nagashima, B. Josse, I. Cionni, M. Righi, V. Eyring, A. Conley, K. W. Bowman, O. Wild, and A. Archibald
Atmos. Chem. Phys., 13, 3063-3085, https://doi.org/10.5194/acp-13-3063-2013, https://doi.org/10.5194/acp-13-3063-2013, 2013
W. J. Collins, M. M. Fry, H. Yu, J. S. Fuglestvedt, D. T. Shindell, and J. J. West
Atmos. Chem. Phys., 13, 2471-2485, https://doi.org/10.5194/acp-13-2471-2013, https://doi.org/10.5194/acp-13-2471-2013, 2013
A. Voulgarakis, V. Naik, J.-F. Lamarque, D. T. Shindell, P. J. Young, M. J. Prather, O. Wild, R. D. Field, D. Bergmann, P. Cameron-Smith, I. Cionni, W. J. Collins, S. B. Dalsøren, R. M. Doherty, V. Eyring, G. Faluvegi, G. A. Folberth, L. W. Horowitz, B. Josse, I. A. MacKenzie, T. Nagashima, D. A. Plummer, M. Righi, S. T. Rumbold, D. S. Stevenson, S. A. Strode, K. Sudo, S. Szopa, and G. Zeng
Atmos. Chem. Phys., 13, 2563-2587, https://doi.org/10.5194/acp-13-2563-2013, https://doi.org/10.5194/acp-13-2563-2013, 2013
Y. H. Lee, J.-F. Lamarque, M. G. Flanner, C. Jiao, D. T. Shindell, T. Berntsen, M. M. Bisiaux, J. Cao, W. J. Collins, M. Curran, R. Edwards, G. Faluvegi, S. Ghan, L. W. Horowitz, J. R. McConnell, J. Ming, G. Myhre, T. Nagashima, V. Naik, S. T. Rumbold, R. B. Skeie, K. Sudo, T. Takemura, F. Thevenon, B. Xu, and J.-H. Yoon
Atmos. Chem. Phys., 13, 2607-2634, https://doi.org/10.5194/acp-13-2607-2013, https://doi.org/10.5194/acp-13-2607-2013, 2013
C. A. Randles, S. Kinne, G. Myhre, M. Schulz, P. Stier, J. Fischer, L. Doppler, E. Highwood, C. Ryder, B. Harris, J. Huttunen, Y. Ma, R. T. Pinker, B. Mayer, D. Neubauer, R. Hitzenberger, L. Oreopoulos, D. Lee, G. Pitari, G. Di Genova, J. Quaas, F. G. Rose, S. Kato, S. T. Rumbold, I. Vardavas, N. Hatzianastassiou, C. Matsoukas, H. Yu, F. Zhang, H. Zhang, and P. Lu
Atmos. Chem. Phys., 13, 2347-2379, https://doi.org/10.5194/acp-13-2347-2013, https://doi.org/10.5194/acp-13-2347-2013, 2013
B. H. Samset, G. Myhre, M. Schulz, Y. Balkanski, S. Bauer, T. K. Berntsen, H. Bian, N. Bellouin, T. Diehl, R. C. Easter, S. J. Ghan, T. Iversen, S. Kinne, A. Kirkevåg, J.-F. Lamarque, G. Lin, X. Liu, J. E. Penner, Ø. Seland, R. B. Skeie, P. Stier, T. Takemura, K. Tsigaridis, and K. Zhang
Atmos. Chem. Phys., 13, 2423-2434, https://doi.org/10.5194/acp-13-2423-2013, https://doi.org/10.5194/acp-13-2423-2013, 2013
N. Bellouin, J. Quaas, J.-J. Morcrette, and O. Boucher
Atmos. Chem. Phys., 13, 2045-2062, https://doi.org/10.5194/acp-13-2045-2013, https://doi.org/10.5194/acp-13-2045-2013, 2013
P. J. Young, A. T. Archibald, K. W. Bowman, J.-F. Lamarque, V. Naik, D. S. Stevenson, S. Tilmes, A. Voulgarakis, O. Wild, D. Bergmann, P. Cameron-Smith, I. Cionni, W. J. Collins, S. B. Dalsøren, R. M. Doherty, V. Eyring, G. Faluvegi, L. W. Horowitz, B. Josse, Y. H. Lee, I. A. MacKenzie, T. Nagashima, D. A. Plummer, M. Righi, S. T. Rumbold, R. B. Skeie, D. T. Shindell, S. A. Strode, K. Sudo, S. Szopa, and G. Zeng
Atmos. Chem. Phys., 13, 2063-2090, https://doi.org/10.5194/acp-13-2063-2013, https://doi.org/10.5194/acp-13-2063-2013, 2013
S. B. Dalsøren, B. H. Samset, G. Myhre, J. J. Corbett, R. Minjares, D. Lack, and J. S. Fuglestvedt
Atmos. Chem. Phys., 13, 1941-1955, https://doi.org/10.5194/acp-13-1941-2013, https://doi.org/10.5194/acp-13-1941-2013, 2013
G. Myhre, B. H. Samset, M. Schulz, Y. Balkanski, S. Bauer, T. K. Berntsen, H. Bian, N. Bellouin, M. Chin, T. Diehl, R. C. Easter, J. Feichter, S. J. Ghan, D. Hauglustaine, T. Iversen, S. Kinne, A. Kirkevåg, J.-F. Lamarque, G. Lin, X. Liu, M. T. Lund, G. Luo, X. Ma, T. van Noije, J. E. Penner, P. J. Rasch, A. Ruiz, Ø. Seland, R. B. Skeie, P. Stier, T. Takemura, K. Tsigaridis, P. Wang, Z. Wang, L. Xu, H. Yu, F. Yu, J.-H. Yoon, K. Zhang, H. Zhang, and C. Zhou
Atmos. Chem. Phys., 13, 1853-1877, https://doi.org/10.5194/acp-13-1853-2013, https://doi.org/10.5194/acp-13-1853-2013, 2013
J.-F. Lamarque, D. T. Shindell, B. Josse, P. J. Young, I. Cionni, V. Eyring, D. Bergmann, P. Cameron-Smith, W. J. Collins, R. Doherty, S. Dalsoren, G. Faluvegi, G. Folberth, S. J. Ghan, L. W. Horowitz, Y. H. Lee, I. A. MacKenzie, T. Nagashima, V. Naik, D. Plummer, M. Righi, S. T. Rumbold, M. Schulz, R. B. Skeie, D. S. Stevenson, S. Strode, K. Sudo, S. Szopa, A. Voulgarakis, and G. Zeng
Geosci. Model Dev., 6, 179-206, https://doi.org/10.5194/gmd-6-179-2013, https://doi.org/10.5194/gmd-6-179-2013, 2013
C. D. Holmes, M. J. Prather, O. A. Søvde, and G. Myhre
Atmos. Chem. Phys., 13, 285-302, https://doi.org/10.5194/acp-13-285-2013, https://doi.org/10.5194/acp-13-285-2013, 2013
Ø. Hodnebrog, T. K. Berntsen, O. Dessens, M. Gauss, V. Grewe, I. S. A. Isaksen, B. Koffi, G. Myhre, D. Olivié, M. J. Prather, F. Stordal, S. Szopa, Q. Tang, P. van Velthoven, and J. E. Williams
Atmos. Chem. Phys., 12, 12211-12225, https://doi.org/10.5194/acp-12-12211-2012, https://doi.org/10.5194/acp-12-12211-2012, 2012
Related subject area
Subject: Aerosols | Research Activity: Atmospheric Modelling | Altitude Range: Troposphere | Science Focus: Physics (physical properties and processes)
Simulation of the transport, vertical distribution, optical properties and radiative impact of smoke aerosols with the ALADIN regional climate model during the ORACLES-2016 and LASIC experiments
BVOC–aerosol–climate feedbacks investigated using NorESM
Potential impacts of cold frontal passage on air quality over the Yangtze River Delta, China
The potential role of methanesulfonic acid (MSA) in aerosol formation and growth and the associated radiative forcings
Aerosol optical properties over Europe: an evaluation of the AQMEII Phase 3 simulations against satellite observations
Accounting for the effects of nonideal minor structures on the optical properties of black carbon aerosols
Interpretation of measured aerosol mass scattering efficiency over North America using a chemical transport model
Simulations of black carbon (BC) aerosol impact over Hindu Kush Himalayan sites: validation, sources, and implications on glacier runoff
Variability, timescales, and nonlinearity in climate responses to black carbon emissions
Local and remote temperature response of regional SO2 emissions
Relationship between Asian monsoon strength and transport of surface aerosols to the Asian Tropopause Aerosol Layer (ATAL): interannual variability and decadal changes
Snow-darkening versus direct radiative effects of mineral dust aerosol on the Indian summer monsoon onset: role of temperature change over dust sources
Influence of cloud microphysical processes on black carbon wet removal, global distributions, and radiative forcing
Open fires in Greenland in summer 2017: transport, deposition and radiative effects of BC, OC and BrC emissions
Modeling the effect of non-ideality, dynamic mass transfer and viscosity on SOA formation in a 3-D air quality model
Studying the impact of biomass burning aerosol radiative and climate effects on the Amazon rainforest productivity with an Earth system model
The value of satellite observations in the analysis and short-range prediction of Asian dust
Modelling black carbon absorption of solar radiation: combining external and internal mixing assumptions
Radiative effect and climate impacts of brown carbon with the Community Atmosphere Model (CAM5)
Contributions to the explosive growth of PM2.5 mass due to aerosol–radiation feedback and decrease in turbulent diffusion during a red alert heavy haze in Beijing–Tianjin–Hebei, China
The impact of mineral dust on cloud formation during the Saharan dust event in April 2014 over Europe
Quantifying uncertainty from aerosol and atmospheric parameters and their impact on climate sensitivity
Insignificant effect of climate change on winter haze pollution in Beijing
H2SO4–H2O–NH3 ternary ion-mediated nucleation (TIMN): kinetic-based model and comparison with CLOUD measurements
The impact of multi-species surface chemical observation assimilation on air quality forecasts in China
Molecular dynamics simulation of the surface tension of aqueous sodium chloride: from dilute to highly supersaturated solutions and molten salt
On the thermodynamic and kinetic aspects of immersion ice nucleation
Effects of brown coatings on the absorption enhancement of black carbon: a numerical investigation
Impacts on cloud radiative effects induced by coexisting aerosols converted from international shipping and maritime DMS emissions
Aerosol water parameterization: long-term evaluation and importance for climate studies
Transport, mixing and feedback of dust, biomass burning and anthropogenic pollutants in eastern Asia: a case study
Investigating the impact of aerosol deposition on snowmelt over the Greenland Ice Sheet using a large-ensemble kernel
Effective radiative forcing in the aerosol–climate model CAM5.3-MARC-ARG
Insights into the morphology of multicomponent organic/inorganic aerosols from molecular dynamics simulations
Simulating the influence of primary biological aerosol particles on clouds by heterogeneous ice nucleation
Top-down estimates of black carbon emissions at high latitudes using an atmospheric transport model and a Bayesian inversion framework
Evaluating cloud properties in an ensemble of regional online coupled models against satellite observations
A thermodynamic description for the hygroscopic growth of atmospheric aerosol particles
Aerosol liquid water content in the moist southern West African monsoon layer and its radiative impact
Assessment of the pollution–health–economics nexus in China
Can semi-volatile organic aerosols lead to fewer cloud particles?
Simulation of the size-composition distribution of atmospheric nanoparticles over Europe
Exploring the potential of nano-Köhler theory to describe the growth of atmospheric molecular clusters by organic vapors using cluster kinetics simulations
Shortwave radiative impact of liquid–liquid phase separation in brown carbon aerosols
The importance of comprehensive parameter sampling and multiple observations for robust constraint of aerosol radiative forcing
Sensitivity of Arctic sulfate aerosol and clouds to changes in future surface seawater dimethylsulfide concentrations
Understanding nitrate formation in a world with less sulfate
Radiative feedbacks of dust in snow over eastern Asia in CAM4-BAM
How reliable are CMIP5 models in simulating dust optical depth?
Constraining nucleation, condensation, and chemistry in oxidation flow reactors using size-distribution measurements and aerosol microphysical modeling
Marc Mallet, Pierre Nabat, Paquita Zuidema, Jens Redemann, Andrew Mark Sayer, Martin Stengel, Sebastian Schmidt, Sabrina Cochrane, Sharon Burton, Richard Ferrare, Kerry Meyer, Pablo Saide, Hiren Jethva, Omar Torres, Robert Wood, David Saint Martin, Romain Roehrig, Christina Hsu, and Paola Formenti
Atmos. Chem. Phys., 19, 4963-4990, https://doi.org/10.5194/acp-19-4963-2019, https://doi.org/10.5194/acp-19-4963-2019, 2019
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The model is able to represent LWP but not the LCF. AOD is consistent over the continent but also over ocean (ACAOD). Differences are observed in SSA due to the absence of internal mixing in ALADIN-Climate. A significant regional gradient of the forcing at TOA is observed. An intense positive forcing is simulated over Gabon. Results highlight the significant effect of enhanced moisture on BBA extinction. The surface dimming modifies the energy budget.
Moa K. Sporre, Sara M. Blichner, Inger H. H. Karset, Risto Makkonen, and Terje K. Berntsen
Atmos. Chem. Phys., 19, 4763-4782, https://doi.org/10.5194/acp-19-4763-2019, https://doi.org/10.5194/acp-19-4763-2019, 2019
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In this study, an Earth system model has been used to investigate climate feedbacks associated with increasing BVOC emissions due to higher CO2 concentrations and temperatures. Higher BVOC emissions associated with a changed climate are found to induce an important negative climate feedback through increased aerosol formation and resulting changes in cloud properties. This feedback is found to have the potential to offset about 13 % of the radiative forcing associated with a doubling of CO2.
Hanqing Kang, Bin Zhu, Jinhui Gao, Yao He, Honglei Wang, Jifeng Su, Chen Pan, Tong Zhu, and Bu Yu
Atmos. Chem. Phys., 19, 3673-3685, https://doi.org/10.5194/acp-19-3673-2019, https://doi.org/10.5194/acp-19-3673-2019, 2019
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In this study, we found that a cold front can transport air pollutants from the polluted North China Plain to the Yangtze River Delta (YRD), thereby deteriorating air quality over the YRD. Before the cold frontal passage, a warm and polluted air mass over YRD climbed to the free troposphere (1.0–2.0 km) along the frontal surface. After the cold frontal passage, high pressure behind the frontal zone resulted in a synoptic subsidence that trapped PM2.5 in the surface.
Anna L. Hodshire, Pedro Campuzano-Jost, John K. Kodros, Betty Croft, Benjamin A. Nault, Jason C. Schroder, Jose L. Jimenez, and Jeffrey R. Pierce
Atmos. Chem. Phys., 19, 3137-3160, https://doi.org/10.5194/acp-19-3137-2019, https://doi.org/10.5194/acp-19-3137-2019, 2019
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A global chemical-transport model is used to determine the impact of methanesulfonic acid (MSA) on the aerosol size distribution and associated radiative effects, testing varying assumptions of MSA’s effective volatility and nucleating ability. We find that MSA mass best matches the ATom airborne measurements when volatility varies as a function of temperature, relative humidity, and available gas-phase bases, and the MSA radiative forcing is on the order of -50 mW m-2 over the Southern Ocean.
Laura Palacios-Peña, Pedro Jiménez-Guerrero, Rocío Baró, Alessandra Balzarini, Roberto Bianconi, Gabriele Curci, Tony Christian Landi, Guido Pirovano, Marje Prank, Angelo Riccio, Paolo Tuccella, and Stefano Galmarini
Atmos. Chem. Phys., 19, 2965-2990, https://doi.org/10.5194/acp-19-2965-2019, https://doi.org/10.5194/acp-19-2965-2019, 2019
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The main uncertainties regarding the estimation of changes in the Earth’s energy budget are related to the role of atmospheric aerosols. Our study evaluates the representation of aerosol optical properties by different atmospheric chemistry models against remote-sensing observations in order to reduce this uncertainty. Results show that the representation of aerosol optical properties is strongly dependent on the used model.
Shiwen Teng, Chao Liu, Martin Schnaiter, Rajan K. Chakrabarty, and Fengshan Liu
Atmos. Chem. Phys., 19, 2917-2931, https://doi.org/10.5194/acp-19-2917-2019, https://doi.org/10.5194/acp-19-2917-2019, 2019
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Black carbon (BC) possesses complex minor structures besides the overall aggregate geometry, thus altering their optical properties. This study introduces volume variation to quantify and unify different minor structures and develops an empirical relation to account for their effects on BC optical properties. We find the effects of minor structures are mainly contributed by their influence on particle volume/mass, and a relative difference of 5 % is noticed after removing volume differences.
Robyn N. C. Latimer and Randall V. Martin
Atmos. Chem. Phys., 19, 2635-2653, https://doi.org/10.5194/acp-19-2635-2019, https://doi.org/10.5194/acp-19-2635-2019, 2019
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Long-term aerosol measurements from the IMPROVE network were used to investigate the simulation of mass scattering efficiency in the GEOS-Chem chemical transport model. The simulation of mass scattering efficiency was developed to better represent observations by refining the representation of aerosol size and hygroscopicity. Simulated average mass scattering efficiency over North America increased by 16 %, with larger increases in northern regions and reductions in the southwest.
Sauvik Santra, Shubha Verma, Koji Fujita, Indrajit Chakraborty, Olivier Boucher, Toshihiko Takemura, John F. Burkhart, Felix Matt, and Mukesh Sharma
Atmos. Chem. Phys., 19, 2441-2460, https://doi.org/10.5194/acp-19-2441-2019, https://doi.org/10.5194/acp-19-2441-2019, 2019
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The present study provided information on specific glaciers over the Hindu Kush Himalayan region identified as being vulnerable to BC-induced impacts (affected by high BC-induced snow albedo reduction in addition to being sensitive to BC-induced impacts), thus impacting the downstream hydrology. The source-specific contribution to atmospheric BC aerosols by emission sources led to identifying the potential emission source, which was distinctive over south and north to 30° N.
Yang Yang, Steven J. Smith, Hailong Wang, Catrin M. Mills, and Philip J. Rasch
Atmos. Chem. Phys., 19, 2405-2420, https://doi.org/10.5194/acp-19-2405-2019, https://doi.org/10.5194/acp-19-2405-2019, 2019
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Black carbon (BC) particles exert a potentially large warming influence on the
Earth system. We evaluate regional climate responses, non-linearity, and short-term transient responses to BC emission perturbations. We found that climate responses do not scale linearity with emissions and BC impacts temperature much faster than greenhouse gas forcing. Removing present-day BC emissions results in discernible surface temperature changes for only limited regions of the globe.
Anna Lewinschal, Annica M. L. Ekman, Hans-Christen Hansson, Maria Sand, Terje K. Berntsen, and Joakim Langner
Atmos. Chem. Phys., 19, 2385-2403, https://doi.org/10.5194/acp-19-2385-2019, https://doi.org/10.5194/acp-19-2385-2019, 2019
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We use a global climate model to study how anthropogenic emissions of short-lived atmospheric particles in different parts of the world influence the global temperature distribution. We find that the global mean temperature change per unit emission is similar for all emission regions, and the largest temperature response is found in the Arctic no matter where the emissions occur. However, for European emissions, the temperature change per unit emission is found to depend on emission strength.
Cheng Yuan, William K. M. Lau, Zhanqing Li, and Maureen Cribb
Atmos. Chem. Phys., 19, 1901-1913, https://doi.org/10.5194/acp-19-1901-2019, https://doi.org/10.5194/acp-19-1901-2019, 2019
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Using MERRA-2 reanalysis daily data from 2001 to 2015, we found that during strong South Asian summer monsoon years, the Asian monsoon anticyclone is more expansive and shifted northward. All the CO, carbonaceous aerosols and dust are found to be more abundant in the Asian Tropopause Aerosol Layer (ATAL). ATAL trends are associated with increasing strength of the AMA, with earlier and enhanced vertical transport of ATAL constituents by enhanced overshooting convection over the transport regions.
Zhengguo Shi, Xiaoning Xie, Xinzhou Li, Liu Yang, Xiaoxun Xie, Jing Lei, Yingying Sha, and Xiaodong Liu
Atmos. Chem. Phys., 19, 1605-1622, https://doi.org/10.5194/acp-19-1605-2019, https://doi.org/10.5194/acp-19-1605-2019, 2019
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Asian dust is one of the important components in modern and past climate change via its effects, including snow-darkening and direct radiation. We employed model experiments to evaluate these effects on Indian monsoon and found that the monsoon onset responds significantly to both. Snow-darkening effect weakens the monsoon, but direct radiative effect intensifies it. Besides the previous Tibetan Plateau studies proposed, our work highlights the importance of temperature change over dust sources.
Jiayu Xu, Jiachen Zhang, Junfeng Liu, Kan Yi, Songlin Xiang, Xiurong Hu, Yuqing Wang, Shu Tao, and George Ban-Weiss
Atmos. Chem. Phys., 19, 1587-1603, https://doi.org/10.5194/acp-19-1587-2019, https://doi.org/10.5194/acp-19-1587-2019, 2019
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In this study, we fully describe black carbon wet removal coupled with all cloud processes from a cloud microphysics scheme in a climate model and conduct sensitivity simulations that turn off each cloud process one at a time. We find that convective scavenging, aerosol activation, ice nucleation, evaporation of rain–snow, and below-cloud scavenging dominate wet deposition of BC. In addition, the range of direct radiative forcing derived from sensitivity simulations is large, 0.09–0.33 W m−2.
Nikolaos Evangeliou, Arve Kylling, Sabine Eckhardt, Viktor Myroniuk, Kerstin Stebel, Ronan Paugam, Sergiy Zibtsev, and Andreas Stohl
Atmos. Chem. Phys., 19, 1393-1411, https://doi.org/10.5194/acp-19-1393-2019, https://doi.org/10.5194/acp-19-1393-2019, 2019
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We simulated the peatland fires that burned in Greenland in summer 2017. Using satellite data, we estimated that the total burned area was 2345 ha, the fuel amount consumed 117 kt C and the emissions of BC, OC and BrC 23.5, 731 and 141 t, respectively. About 30 % of the emissions were deposited on snow or ice surfaces. This caused a maximum albedo change of 0.007 and a surface radiative forcing of 0.03–0.04 W m−2, with local maxima of up to 0.63–0.77 W m−2. Overall, the fires had a small impact.
Youngseob Kim, Karine Sartelet, and Florian Couvidat
Atmos. Chem. Phys., 19, 1241-1261, https://doi.org/10.5194/acp-19-1241-2019, https://doi.org/10.5194/acp-19-1241-2019, 2019
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Assumptions (ideality and thermodynamic equilibrium) commonly made in 3-dimensional air quality models were reconsidered to evaluate their impacts on secondary organic aerosol (SOA) formation. Non-ideality (short-, medium- and long-range interactions of organics and inorganics) influences SOA concentrations by about 30 % over Europe. If SOA are highly viscous rather than inviscid, hydrophobic SOA concentrations increase by 6 % but can increase by an order of magnitude for volatile compounds.
Florent F. Malavelle, Jim M. Haywood, Lina M. Mercado, Gerd A. Folberth, Nicolas Bellouin, Stephen Sitch, and Paulo Artaxo
Atmos. Chem. Phys., 19, 1301-1326, https://doi.org/10.5194/acp-19-1301-2019, https://doi.org/10.5194/acp-19-1301-2019, 2019
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Diffuse light can increase the efficiency of vegetation photosynthesis. Diffuse light results from scattering by either clouds or aerosols in the atmosphere. During the dry season biomass burning (BB) on the edges of the Amazon rainforest contributes significantly to the aerosol burden over the entire region. We show that despite a modest effect of change in light conditions, the overall impact of BB aerosols on the vegetation is still important when indirect climate feedbacks are considered.
Angela Benedetti, Francesca Di Giuseppe, Luke Jones, Vincent-Henri Peuch, Samuel Rémy, and Xiaoye Zhang
Atmos. Chem. Phys., 19, 987-998, https://doi.org/10.5194/acp-19-987-2019, https://doi.org/10.5194/acp-19-987-2019, 2019
Gabriele Curci, Ummugulsum Alyuz, Rocio Barò, Roberto Bianconi, Johannes Bieser, Jesper H. Christensen, Augustin Colette, Aidan Farrow, Xavier Francis, Pedro Jiménez-Guerrero, Ulas Im, Peng Liu, Astrid Manders, Laura Palacios-Peña, Marje Prank, Luca Pozzoli, Ranjeet Sokhi, Efisio Solazzo, Paolo Tuccella, Alper Unal, Marta G. Vivanco, Christian Hogrefe, and Stefano Galmarini
Atmos. Chem. Phys., 19, 181-204, https://doi.org/10.5194/acp-19-181-2019, https://doi.org/10.5194/acp-19-181-2019, 2019
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Atmospheric carbonaceous aerosols are able to absorb solar radiation and they continue to contribute some of the largest uncertainties in projected climate change. One important detail is how the chemical species are arranged inside each particle, i.e. the knowledge of their mixing state. We use an ensemble of regional model simulations to test different mixing state assumptions and found that a combination of internal and external mixing may better reproduce sunphotometer observations.
Hunter Brown, Xiaohong Liu, Yan Feng, Yiquan Jiang, Mingxuan Wu, Zheng Lu, Chenglai Wu, Shane Murphy, and Rudra Pokhrel
Atmos. Chem. Phys., 18, 17745-17768, https://doi.org/10.5194/acp-18-17745-2018, https://doi.org/10.5194/acp-18-17745-2018, 2018
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In climate models, organic carbon (OC) in wildfire smoke has been treated as an atmospheric cooling component by reflecting sunlight back to space. This study incorporates the observationally identified absorbing brown carbon component of OC into the Community Earth System Model, improving the agreement between the model and observations and effectively increasing absorption of solar radiation. This change contributes to altered atmospheric dynamics and changes in cloud cover in the model.
Hong Wang, Yue Peng, Xiaoye Zhang, Hongli Liu, Meng Zhang, Huizheng Che, Yanli Cheng, and Yu Zheng
Atmos. Chem. Phys., 18, 17717-17733, https://doi.org/10.5194/acp-18-17717-2018, https://doi.org/10.5194/acp-18-17717-2018, 2018
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The explosive growth (EG) of PM2.5 resulted in a PM2.5 maximum, which was generally underestimated by atmospheric chemical models due to the deficient description of the local
turbulence intermittent. The aerosol–radiation feedback (AF) and decrease in turbulence diffusion (DTD) may reduce the underestimation of PM2.5 EG by 20–25% and 14–20%, respectively. The modeled EG stage PM2.5 error was decreased from −40 to −51% to −11 to 2% by the combined effects of AF and DTD in Jing–Jin–Ji.
Michael Weger, Bernd Heinold, Christa Engler, Ulrich Schumann, Axel Seifert, Romy Fößig, Christiane Voigt, Holger Baars, Ulrich Blahak, Stephan Borrmann, Corinna Hoose, Stefan Kaufmann, Martina Krämer, Patric Seifert, Fabian Senf, Johannes Schneider, and Ina Tegen
Atmos. Chem. Phys., 18, 17545-17572, https://doi.org/10.5194/acp-18-17545-2018, https://doi.org/10.5194/acp-18-17545-2018, 2018
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The impact of desert dust on cloud formation is investigated for a major Saharan dust event over Europe by interactive regional dust modeling. Dust particles are very efficient ice-nucleating particles promoting the formation of ice crystals in clouds. The simulations show that the observed extensive cirrus development was likely related to the above-average dust load. The interactive dust–cloud feedback in the model significantly improves the agreement with aircraft and satellite observations.
Christopher G. Fletcher, Ben Kravitz, and Bakr Badawy
Atmos. Chem. Phys., 18, 17529-17543, https://doi.org/10.5194/acp-18-17529-2018, https://doi.org/10.5194/acp-18-17529-2018, 2018
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The most important number for future climate projections is Earth's climate sensitivity (CS), or how much warming will result from increased carbon dioxide. We cannot know the true CS, and estimates of CS from climate models have a wide range. This study identifies the major factors that control this range, and we show that the choice of methods used in creating a climate model are three times more important than fine-tuning the details of the model after it is created.
Lu Shen, Daniel J. Jacob, Loretta J. Mickley, Yuxuan Wang, and Qiang Zhang
Atmos. Chem. Phys., 18, 17489-17496, https://doi.org/10.5194/acp-18-17489-2018, https://doi.org/10.5194/acp-18-17489-2018, 2018
Fangqun Yu, Alexey B. Nadykto, Jason Herb, Gan Luo, Kirill M. Nazarenko, and Lyudmila A. Uvarova
Atmos. Chem. Phys., 18, 17451-17474, https://doi.org/10.5194/acp-18-17451-2018, https://doi.org/10.5194/acp-18-17451-2018, 2018
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Aerosol nucleation exerts important influences on the climate, hydrological cycle, and air quality. We have developed an advanced physical–chemical model that describes ion-induced and neutral nucleation involving ammonia, sulfuric acid, and water vapors. The model is shown to reproduce laboratory measurements taken under a wide range of conditions, offers physiochemical insights into the ternary nucleation process, and provides an accurate approach to calculate ternary rate in the atmosphere.
Zhen Peng, Lili Lei, Zhiquan Liu, Jianning Sun, Aijun Ding, Junmei Ban, Dan Chen, Xingxia Kou, and Kekuan Chu
Atmos. Chem. Phys., 18, 17387-17404, https://doi.org/10.5194/acp-18-17387-2018, https://doi.org/10.5194/acp-18-17387-2018, 2018
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An EnKF system was developed to simultaneously assimilate multiple surface measurements, including PM10, PM2.5, SO2, NO2, O3, and CO, via the joint adjustment of ICs and source emissions. Large improvements were achieved in the first 24 h forecast for PM2.5, PM10, SO2, and CO during an extreme haze episode that occurred in early October 2014 over the North China Plain, but no improvements were achieved for NO2 and O3.
Xiaoxiang Wang, Chuchu Chen, Kurt Binder, Uwe Kuhn, Ulrich Pöschl, Hang Su, and Yafang Cheng
Atmos. Chem. Phys., 18, 17077-17086, https://doi.org/10.5194/acp-18-17077-2018, https://doi.org/10.5194/acp-18-17077-2018, 2018
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The surface tension of aqueous NaCl (σ) is investigated by molecular dynamics simulations from dilute to highly supersaturated solutions. The linear approximation of concentration dependence of σ at molality scale can be extended to the supersaturated NaCl solution until the solute mass fraction (xNaCl) of ~0.39. After that, the σ remains almost unchanged until an xNaCl of ~0.47. Then the σ gradually regains the growing momentum with a tendency to approach the surface tension of molten NaCl.
Donifan Barahona
Atmos. Chem. Phys., 18, 17119-17141, https://doi.org/10.5194/acp-18-17119-2018, https://doi.org/10.5194/acp-18-17119-2018, 2018
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This work develops a model for ice formation mediated by particles immersed within droplets. Ice nucleation is not only enhanced by the modification of the thermodynamic properties of the vicinal water but is also inhibited by decreased water mobility near the particle. The ice nucleation rate is thus determined by competing kinetic and thermodynamic factors during ice formation. A new regime where ice nucleation is mediated mainly by kinetics instead of thermodynamics is discovered.
Jie Luo, Yongming Zhang, Feng Wang, and Qixing Zhang
Atmos. Chem. Phys., 18, 16897-16914, https://doi.org/10.5194/acp-18-16897-2018, https://doi.org/10.5194/acp-18-16897-2018, 2018
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The absorption enhancement of black carbon with brown coatings is investigated. In addition, the ratio of the absorption of BC coated by brown carbon (BrC) to an external mixture of BrC and BC (Eabs_internal) is also investigated. The lensing effect and sunglasses effect are clearly defined. The applicability of the core–shell sphere model was investigated. The effects of the size distribution, fractal dimension, and wavelength dependency are also explored.
Qinjian Jin, Benjamin S. Grandey, Daniel Rothenberg, Alexander Avramov, and Chien Wang
Atmos. Chem. Phys., 18, 16793-16808, https://doi.org/10.5194/acp-18-16793-2018, https://doi.org/10.5194/acp-18-16793-2018, 2018
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International shipping emissions (ISE) can influence the global radiation budget. Using an Earth system model, we derive a significant global cloud radiative effect (CRE) of ISE (−0.153 W m−2) when using current emissions. This CRE would become weaker (−0.001 W m−2) if a more stringent regulation were adopted. The CRE would achieve a significant enhancement when a lower DMS emission is prescribed. These findings suggest a reevaluation of the ISE-induced CRE with consideration of DMS variability.
Swen Metzger, Mohamed Abdelkader, Benedikt Steil, and Klaus Klingmüller
Atmos. Chem. Phys., 18, 16747-16774, https://doi.org/10.5194/acp-18-16747-2018, https://doi.org/10.5194/acp-18-16747-2018, 2018
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This paper discusses the importance of aerosol water for aerosol optical depth calculations using a long-term evaluation of the global chemistry climate and Earth system model EMAC through a comparison of EQSAM4clim and ISORROPIA II with observations at climate timescales. Sensitivity studies with different levels of chemical aging and associated water uptake demonstrate the importance of aerosol water for climate modeling studies.
Derong Zhou, Ke Ding, Xin Huang, Lixia Liu, Qiang Liu, Zhengning Xu, Fei Jiang, Congbin Fu, and Aijun Ding
Atmos. Chem. Phys., 18, 16345-16361, https://doi.org/10.5194/acp-18-16345-2018, https://doi.org/10.5194/acp-18-16345-2018, 2018
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We investigate the vertical distribution, transport characteristics, source contribution and meteorological feedback of dust, biomass burning and fossil fuel combustion aerosols for a unique pollution episode that occurred in late March 2015 in eastern Asia, based on various measurement data and modeling methods. We found that cold front played an important role in the long-range transport of different pollutants and caused a three-layer vertical structure of pollutants over eastern China.
Yang Li and Mark G. Flanner
Atmos. Chem. Phys., 18, 16005-16018, https://doi.org/10.5194/acp-18-16005-2018, https://doi.org/10.5194/acp-18-16005-2018, 2018
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Light-absorbing impurities enhance snowmelt by boosting the absorption of solar energy. It is therefore important for coupled aerosol–climate and ice sheet models to include this effect, and yet most do not. We conduct several thousand simulations and develop a kernel and linear equations relating melt runoff on the Greenland Ice Sheet to the timing and amount of black carbon within precipitation and dry deposition, which can be used to extend the utility of state-of-the-art aerosol models.
Benjamin S. Grandey, Daniel Rothenberg, Alexander Avramov, Qinjian Jin, Hsiang-He Lee, Xiaohong Liu, Zheng Lu, Samuel Albani, and Chien Wang
Atmos. Chem. Phys., 18, 15783-15810, https://doi.org/10.5194/acp-18-15783-2018, https://doi.org/10.5194/acp-18-15783-2018, 2018
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Anthropogenic emissions of aerosol particles likely cool the climate system. We investigate the uncertainty in the strength of the cooling effect by exploring the representation of aerosols in a global climate model. We conclude that the specific representation of aerosols in global climate models has important implications for climate modelling. Important factors include the representation of aerosol mixing state, size distribution, and optical properties.
Katerina S. Karadima, Vlasis G. Mavrantzas, and Spyros N. Pandis
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2018-1098, https://doi.org/10.5194/acp-2018-1098, 2018
Revised manuscript accepted for ACP
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We explore the morphologies of multicomponent nanoparticles through atomistic molecular dynamics simulations under atmospherically relevant conditions. Phase separation is predicted for almost all simulated nanoparticles either between organics and inorganics or between hydrophobic and hydrophilic constituents. Three main particle types were identified: organic islands at the surface, inorganic core-organic shell morphologies, and complex structures with hydrophobic and hydrophilic domains.
Matthias Hummel, Corinna Hoose, Bernhard Pummer, Caroline Schaupp, Janine Fröhlich-Nowoisky, and Ottmar Möhler
Atmos. Chem. Phys., 18, 15437-15450, https://doi.org/10.5194/acp-18-15437-2018, https://doi.org/10.5194/acp-18-15437-2018, 2018
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How important for clouds is the ability of biological particles to glaciate droplets at little supercooling? In a case study, the regional atmospheric model COSMO–ART is used. Perturbed and control runs are compared.
The number of ice particles that are nucleated by biological particles is highest at around −10 °C. No significant influence on the average state of the cloud ice phase was found. However, the number of ice crystals is slightly enhanced in the absence of other ice nucleators.
Nikolaos Evangeliou, Rona L. Thompson, Sabine Eckhardt, and Andreas Stohl
Atmos. Chem. Phys., 18, 15307-15327, https://doi.org/10.5194/acp-18-15307-2018, https://doi.org/10.5194/acp-18-15307-2018, 2018
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We present BC inversions at high northern latitudes in 2013–2015. The emissions were high close to the gas flaring regions in Russia and in western Canada. The posterior emissions of BC at latitudes > 50° N were estimated as 560 ± 171 kt yr-1, smaller than in bottom-up inventories. Posterior concentrations over the Arctic compared with independent observations from flight and ship campaigns showed small biases. Seasonal maxima were estimated in summer months due to biomass burning, mainly in Europe.
Rocío Baró, Pedro Jiménez-Guerrero, Martin Stengel, Dominik Brunner, Gabriele Curci, Renate Forkel, Lucy Neal, Laura Palacios-Peña, Nicholas Savage, Martijn Schaap, Paolo Tuccella, Hugo Denier van der Gon, and Stefano Galmarini
Atmos. Chem. Phys., 18, 15183-15199, https://doi.org/10.5194/acp-18-15183-2018, https://doi.org/10.5194/acp-18-15183-2018, 2018
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Particles in the atmosphere, such as pollution, desert dust, and volcanic ash, have an impact on meteorology. They interact with incoming radiation resulting in a cooling effect of the atmosphere. Today, the use of meteorology and chemistry models help us to understand these processes, but there are a lot of uncertainties. The goal of this work is to evaluate how these interactions are represented in the models by comparing them to satellite data to see how close they are to reality.
Dimitri Castarède and Erik S. Thomson
Atmos. Chem. Phys., 18, 14939-14948, https://doi.org/10.5194/acp-18-14939-2018, https://doi.org/10.5194/acp-18-14939-2018, 2018
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We present a new description for the continuous transition of soluble atmospheric particulate from dry to completely dissolved particles. The theoretical development is motivated by observations that suggest particle surfaces begin to dissolve even at very low relative humidities. The results extend the understanding of the potential phase behavior of atmospheric particles with a wide range of implications.
Konrad Deetz, Heike Vogel, Sophie Haslett, Peter Knippertz, Hugh Coe, and Bernhard Vogel
Atmos. Chem. Phys., 18, 14271-14295, https://doi.org/10.5194/acp-18-14271-2018, https://doi.org/10.5194/acp-18-14271-2018, 2018
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Water uptake can significantly increase the size and therefore alters the optical properties of aerosols. Our model study reveals that the high moisture and aerosol burden in the southern West African monsoon
layer makes it favorable to quantify properties that determine the aerosol liquid water content and its impact on the aerosol optical depth and radiative transfer. Especially in moist tropical environments the relative humidity impact on AOD has to be considered in atmospheric models.
Yang Xia, Dabo Guan, Jing Meng, Yuan Li, and Yuli Shan
Atmos. Chem. Phys., 18, 14433-14443, https://doi.org/10.5194/acp-18-14433-2018, https://doi.org/10.5194/acp-18-14433-2018, 2018
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Economic loss from disease-induced working time loss reached CNY 398 billion in China 2012. Most is from Eastern and Mid-South China. Mid-South, North, and Eastern China showed most indirect loss. Indirect loss in North, Northwest, and Southwest China is from manufacturing and energy from other regions, while loss in Eastern, Mid-South, and Northeast China is from coal and mining, implying the role of distance in regional links and varied regional loss due to different economic dependencies.
Chloe Y. Gao, Susanne E. Bauer, and Kostas Tsigaridis
Atmos. Chem. Phys., 18, 14243-14251, https://doi.org/10.5194/acp-18-14243-2018, https://doi.org/10.5194/acp-18-14243-2018, 2018
David Patoulias, Christos Fountoukis, Ilona Riipinen, Ari Asmi, Markku Kulmala, and Spyros N. Pandis
Atmos. Chem. Phys., 18, 13639-13654, https://doi.org/10.5194/acp-18-13639-2018, https://doi.org/10.5194/acp-18-13639-2018, 2018
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PMCAMx-UF, a 3-D chemical transport model focusing on the simulation of ultrafine particles, has been extended with the addition of the volatility basis set (VBS) approach for the simulation of organic aerosol. The model was applied in Europe and its predictions were evaluated against field observations collected during the PEGASOS 2012 campaign. The condensation of organics led to an increase (50–120 %) in the larger particles but the total number concentration decreased by 10–30 %.
Jenni Kontkanen, Tinja Olenius, Markku Kulmala, and Ilona Riipinen
Atmos. Chem. Phys., 18, 13733-13754, https://doi.org/10.5194/acp-18-13733-2018, https://doi.org/10.5194/acp-18-13733-2018, 2018
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New particle formation involving sulfuric acid, bases and organic compounds is an important source of atmospheric aerosol particles. We investigate the capability of nano-Köhler theory to describe this process by simulating the dynamics of atmospheric molecular clusters. We find that nano-Köhler-type behavior occurs in our simulations when the saturation ratio of the organic vapor and the ratio between organic and inorganic vapor concentrations are in a suitable range.
Mehrnoush M. Fard, Ulrich K. Krieger, and Thomas Peter
Atmos. Chem. Phys., 18, 13511-13530, https://doi.org/10.5194/acp-18-13511-2018, https://doi.org/10.5194/acp-18-13511-2018, 2018
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Atmospheric aerosol particles may undergo liquid–liquid phase separation (LLPS) when exposed to varying relative humidity, with an aqueous organic phase enclosing an aqueous inorganic phase below a threshold of relative humidity. Brown carbon (BrC) compounds will redistribute to the organic phase upon LLPS. We use numerical modeling to study the shortwave radiative impact of LLPS containing BrC and conclude that it is not significant for atmospheric aerosol.
Jill S. Johnson, Leighton A. Regayre, Masaru Yoshioka, Kirsty J. Pringle, Lindsay A. Lee, David M. H. Sexton, John W. Rostron, Ben B. B. Booth, and Kenneth S. Carslaw
Atmos. Chem. Phys., 18, 13031-13053, https://doi.org/10.5194/acp-18-13031-2018, https://doi.org/10.5194/acp-18-13031-2018, 2018
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We estimate the uncertainty in an aerosol–climate model that has been tuned to match several common types of observations. We used a large set of model simulations and built emulators so that we could generate 4 million “variants” of our climate model. Even after using nine aerosol and cloud observations to constrain the model, the uncertainty remains large. We conclude that estimates of aerosol forcing from multi-model studies are likely to be more uncertain than currently estimated.
Rashed Mahmood, Knut von Salzen, Ann-Lise Norman, Martí Galí, and Maurice Levasseur
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2018-876, https://doi.org/10.5194/acp-2018-876, 2018
Revised manuscript accepted for ACP
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This study evaluates impacts of surface seawater dimethylsulfide on Arctic sulfate aerosol budget, changes in cloud droplet number concentration (CDNC), and cloud radiative forcing under current and future sea ice conditions using an atmospheric global climate model. In the future, sulfate wet removal efficiency is increased by enhanced precipitation, however, simulated aerosol nucleation rates are higher, which result in an overall increase in CDNC and negative cloud radiative forcing.
Petros Vasilakos, Armistead Russell, Rodney Weber, and Athanasios Nenes
Atmos. Chem. Phys., 18, 12765-12775, https://doi.org/10.5194/acp-18-12765-2018, https://doi.org/10.5194/acp-18-12765-2018, 2018
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In this work, we investigated the role of emission reductions on aerosol acidity and particulate nitrate. We found that models exhibit positive biases in pH predictions, attributed to very high levels of crustal elements (Mg, Ca, K) in model simulations, which in turn led to an increasing aerosol pH trend over the past decade and allowed nitrate to become an important component of aerosol, which is inconsistent with the measurements, highlighting the importance of accurate pH prediction.
Xiaoning Xie, Xiaodong Liu, Huizheng Che, Xiaoxun Xie, Xinzhou Li, Zhengguo Shi, Hongli Wang, Tianliang Zhao, and Yangang Liu
Atmos. Chem. Phys., 18, 12683-12698, https://doi.org/10.5194/acp-18-12683-2018, https://doi.org/10.5194/acp-18-12683-2018, 2018
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This study extends our previous investigation in dust–radiation interactions to investigate SRF and its feedbacks on the regional climate and the dust cycle over east Asia by use of the CAM4-BAM. Our results show that SRF increases the east Asian dust emissions significantly by 13.7 % in the spring, in contrast to −7.6 % of decreased dust emissions by DRF. Hence, a significant feature of SRF on the Tibetan Plateau can create a positive feedback loop to enhance the dust cycle over east Asia.
Bing Pu and Paul Ginoux
Atmos. Chem. Phys., 18, 12491-12510, https://doi.org/10.5194/acp-18-12491-2018, https://doi.org/10.5194/acp-18-12491-2018, 2018
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Biases in dust modeling may result in biases in simulating energy budget and regional climate. Output of seven Coupled Model Intercomparison Project Phase 5 (CMIP5) models is examined. Seasonal cycle and spatial pattern of dust optical depth (DOD) in very dusty regions are largely captured by multi-model mean. But observed connections between DOD and local controlling factors such as bareness are not well represented. Future projections by CMIP5 models and a regression model are also analyzed.
Anna L. Hodshire, Brett B. Palm, M. Lizabeth Alexander, Qijing Bian, Pedro Campuzano-Jost, Eben S. Cross, Douglas A. Day, Suzane S. de Sá, Alex B. Guenther, Armin Hansel, James F. Hunter, Werner Jud, Thomas Karl, Saewung Kim, Jesse H. Kroll, Jeong-Hoo Park, Zhe Peng, Roger Seco, James N. Smith, Jose L. Jimenez, and Jeffrey R. Pierce
Atmos. Chem. Phys., 18, 12433-12460, https://doi.org/10.5194/acp-18-12433-2018, https://doi.org/10.5194/acp-18-12433-2018, 2018
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We investigate the nucleation and growth processes that shape the aerosol size distribution inside oxidation flow reactors (OFRs) that sampled ambient air from Colorado and the Amazon rainforest. Results indicate that organics are important for both nucleation and growth, vapor uptake was limited to accumulation-mode particles, fragmentation reactions were important to limit particle growth at higher OH exposures, and an H2SO4-organics nucleation mechanism captured new particle formation well.
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Short summary
We investigate the impact of removing land-based anthropogenic emissions of three aerosol species, using four fully-coupled atmosphere-ocean global climate models. Removing SO2 emissions leads to warming globally, strongest in the Northern Hemisphere (NH), and an increase in NH precipitation. Organic and black carbon (OC, BC) have a weaker impact, and less certainty on the response; OC (BC) removal shows a weak overall warming (cooling), and both show small increases in precipitation globally.
We investigate the impact of removing land-based anthropogenic emissions of three aerosol...
Atmospheric Chemistry and Physics
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