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Composition changes after the "Halloween" solar proton event : the High Energy Particle Precipitation in the Atmosphere (HEPPA) model versus MIPAS data intercomparison study. / Funke, B.; Baumgaertner, A.; Calisto, M.; Egorova, T.; Jackman, C. H.; Kieser, J.; Krivolutsky, A.; Lopez-Puertas, M.; Marsh, D. R.; Reddmann, T.; Rozanov, E.; Salmi, S. -M.; Sinnhuber, M.; Stiller, G. P.; Verronen, P. T.; Versick, S.; von Clarmann, T.; Vyushkova, T. Y.; Wieters, N.; Wissing, J. M.

In: Atmospheric Chemistry and Physics, Vol. 11, No. 17, 2011, p. 9089-9139.

Research output: Contribution to journalArticlepeer-review

Harvard

Funke, B, Baumgaertner, A, Calisto, M, Egorova, T, Jackman, CH, Kieser, J, Krivolutsky, A, Lopez-Puertas, M, Marsh, DR, Reddmann, T, Rozanov, E, Salmi, S-M, Sinnhuber, M, Stiller, GP, Verronen, PT, Versick, S, von Clarmann, T, Vyushkova, TY, Wieters, N & Wissing, JM 2011, 'Composition changes after the "Halloween" solar proton event: the High Energy Particle Precipitation in the Atmosphere (HEPPA) model versus MIPAS data intercomparison study', Atmospheric Chemistry and Physics, vol. 11, no. 17, pp. 9089-9139. https://doi.org/10.5194/acp-11-9089-2011

APA

Funke, B., Baumgaertner, A., Calisto, M., Egorova, T., Jackman, C. H., Kieser, J., Krivolutsky, A., Lopez-Puertas, M., Marsh, D. R., Reddmann, T., Rozanov, E., Salmi, S. -M., Sinnhuber, M., Stiller, G. P., Verronen, P. T., Versick, S., von Clarmann, T., Vyushkova, T. Y., Wieters, N., & Wissing, J. M. (2011). Composition changes after the "Halloween" solar proton event: the High Energy Particle Precipitation in the Atmosphere (HEPPA) model versus MIPAS data intercomparison study. Atmospheric Chemistry and Physics, 11(17), 9089-9139. https://doi.org/10.5194/acp-11-9089-2011

Vancouver

Author

Funke, B. ; Baumgaertner, A. ; Calisto, M. ; Egorova, T. ; Jackman, C. H. ; Kieser, J. ; Krivolutsky, A. ; Lopez-Puertas, M. ; Marsh, D. R. ; Reddmann, T. ; Rozanov, E. ; Salmi, S. -M. ; Sinnhuber, M. ; Stiller, G. P. ; Verronen, P. T. ; Versick, S. ; von Clarmann, T. ; Vyushkova, T. Y. ; Wieters, N. ; Wissing, J. M. / Composition changes after the "Halloween" solar proton event : the High Energy Particle Precipitation in the Atmosphere (HEPPA) model versus MIPAS data intercomparison study. In: Atmospheric Chemistry and Physics. 2011 ; Vol. 11, No. 17. pp. 9089-9139.

BibTeX

@article{58ec99614c1043e9a0d3c27eea01fa67,
title = "Composition changes after the {"}Halloween{"} solar proton event: the High Energy Particle Precipitation in the Atmosphere (HEPPA) model versus MIPAS data intercomparison study",
abstract = "We have compared composition changes of NO, NO2, H2O2, O-3, N2O, HNO3, N2O5, HNO4, ClO, HOCl, and ClONO2 as observed by the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) on Envisat in the aftermath of the {"}Halloween{"} solar proton event (SPE) in late October 2003 at 25-0.01 hPa in the Northern Hemisphere (40-90 degrees N) and simulations performed by the following atmospheric models: the Bremen 2-D model (B2dM) and Bremen 3-D Chemical Transport Model (B3dCTM), the Central Aerological Observatory (CAO) model, Fin-ROSE, the Hamburg Model of the Neutral and Ionized Atmosphere (HAMMONIA), the Karlsruhe Simulation Model of the Middle Atmosphere (KASIMA), the ECHAM5/MESSy Atmospheric Chemistry (EMAC) model, the modeling tool for SOlar Climate Ozone Links studies (SOCOL and SOCOLi), and the Whole Atmosphere Community Climate Model (WACCM4). The large number of participating models allowed for an evaluation of the overall ability of atmospheric models to reproduce observed atmospheric perturbations generated by SPEs, particularly with respect to NOy and ozone changes. We have further assessed the meteorological conditions and their implications for the chemical response to the SPE in both the models and observations by comparing temperature and tracer (CH4 and CO) fields.Simulated SPE-induced ozone losses agree on average within 5% with the observations. Simulated NOy enhancements around 1 hPa, however, are typically 30% higher than indicated by the observations which are likely to be related to deficiencies in the used ionization rates, though other error sources related to the models' atmospheric background state and/or transport schemes cannot be excluded. The analysis of the observed and modeled NOy partitioning in the aftermath of the SPE has demonstrated the need to implement additional ion chemistry (HNO3 formation via ion-ion recombination and water cluster ions) into the chemical schemes. An overestimation of observed H2O2 enhancements by all models hints at an underestimation of the OH/HO2 ratio in the upper polar stratosphere during the SPE. The analysis of chlorine species perturbations has shown that the encountered differences between models and observations, particularly the underestimation of observed ClONO2 enhancements, are related to a smaller availability of ClO in the polar night region already before the SPE. In general, the intercomparison has demonstrated that differences in the meteorology and/or initial state of the atmosphere in the simulations cause a relevant variability of the model results, even on a short timescale of only a few days.",
keywords = "OCTOBER-NOVEMBER 2003, CHEMISTRY-CLIMATE MODEL, MIDDLE ATMOSPHERE, MICHELSON INTERFEROMETER, SOUNDING MIPAS, OZONE DEPLETION, TECHNICAL NOTE, ION CHEMISTRY, HNO3, VALIDATION",
author = "B. Funke and A. Baumgaertner and M. Calisto and T. Egorova and Jackman, {C. H.} and J. Kieser and A. Krivolutsky and M. Lopez-Puertas and Marsh, {D. R.} and T. Reddmann and E. Rozanov and Salmi, {S. -M.} and M. Sinnhuber and Stiller, {G. P.} and Verronen, {P. T.} and S. Versick and {von Clarmann}, T. and Vyushkova, {T. Y.} and N. Wieters and Wissing, {J. M.}",
year = "2011",
doi = "10.5194/acp-11-9089-2011",
language = "Английский",
volume = "11",
pages = "9089--9139",
journal = "Atmospheric Chemistry and Physics",
issn = "1680-7316",
publisher = "Copernicus GmbH ",
number = "17",

}

RIS

TY - JOUR

T1 - Composition changes after the "Halloween" solar proton event

T2 - the High Energy Particle Precipitation in the Atmosphere (HEPPA) model versus MIPAS data intercomparison study

AU - Funke, B.

AU - Baumgaertner, A.

AU - Calisto, M.

AU - Egorova, T.

AU - Jackman, C. H.

AU - Kieser, J.

AU - Krivolutsky, A.

AU - Lopez-Puertas, M.

AU - Marsh, D. R.

AU - Reddmann, T.

AU - Rozanov, E.

AU - Salmi, S. -M.

AU - Sinnhuber, M.

AU - Stiller, G. P.

AU - Verronen, P. T.

AU - Versick, S.

AU - von Clarmann, T.

AU - Vyushkova, T. Y.

AU - Wieters, N.

AU - Wissing, J. M.

PY - 2011

Y1 - 2011

N2 - We have compared composition changes of NO, NO2, H2O2, O-3, N2O, HNO3, N2O5, HNO4, ClO, HOCl, and ClONO2 as observed by the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) on Envisat in the aftermath of the "Halloween" solar proton event (SPE) in late October 2003 at 25-0.01 hPa in the Northern Hemisphere (40-90 degrees N) and simulations performed by the following atmospheric models: the Bremen 2-D model (B2dM) and Bremen 3-D Chemical Transport Model (B3dCTM), the Central Aerological Observatory (CAO) model, Fin-ROSE, the Hamburg Model of the Neutral and Ionized Atmosphere (HAMMONIA), the Karlsruhe Simulation Model of the Middle Atmosphere (KASIMA), the ECHAM5/MESSy Atmospheric Chemistry (EMAC) model, the modeling tool for SOlar Climate Ozone Links studies (SOCOL and SOCOLi), and the Whole Atmosphere Community Climate Model (WACCM4). The large number of participating models allowed for an evaluation of the overall ability of atmospheric models to reproduce observed atmospheric perturbations generated by SPEs, particularly with respect to NOy and ozone changes. We have further assessed the meteorological conditions and their implications for the chemical response to the SPE in both the models and observations by comparing temperature and tracer (CH4 and CO) fields.Simulated SPE-induced ozone losses agree on average within 5% with the observations. Simulated NOy enhancements around 1 hPa, however, are typically 30% higher than indicated by the observations which are likely to be related to deficiencies in the used ionization rates, though other error sources related to the models' atmospheric background state and/or transport schemes cannot be excluded. The analysis of the observed and modeled NOy partitioning in the aftermath of the SPE has demonstrated the need to implement additional ion chemistry (HNO3 formation via ion-ion recombination and water cluster ions) into the chemical schemes. An overestimation of observed H2O2 enhancements by all models hints at an underestimation of the OH/HO2 ratio in the upper polar stratosphere during the SPE. The analysis of chlorine species perturbations has shown that the encountered differences between models and observations, particularly the underestimation of observed ClONO2 enhancements, are related to a smaller availability of ClO in the polar night region already before the SPE. In general, the intercomparison has demonstrated that differences in the meteorology and/or initial state of the atmosphere in the simulations cause a relevant variability of the model results, even on a short timescale of only a few days.

AB - We have compared composition changes of NO, NO2, H2O2, O-3, N2O, HNO3, N2O5, HNO4, ClO, HOCl, and ClONO2 as observed by the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) on Envisat in the aftermath of the "Halloween" solar proton event (SPE) in late October 2003 at 25-0.01 hPa in the Northern Hemisphere (40-90 degrees N) and simulations performed by the following atmospheric models: the Bremen 2-D model (B2dM) and Bremen 3-D Chemical Transport Model (B3dCTM), the Central Aerological Observatory (CAO) model, Fin-ROSE, the Hamburg Model of the Neutral and Ionized Atmosphere (HAMMONIA), the Karlsruhe Simulation Model of the Middle Atmosphere (KASIMA), the ECHAM5/MESSy Atmospheric Chemistry (EMAC) model, the modeling tool for SOlar Climate Ozone Links studies (SOCOL and SOCOLi), and the Whole Atmosphere Community Climate Model (WACCM4). The large number of participating models allowed for an evaluation of the overall ability of atmospheric models to reproduce observed atmospheric perturbations generated by SPEs, particularly with respect to NOy and ozone changes. We have further assessed the meteorological conditions and their implications for the chemical response to the SPE in both the models and observations by comparing temperature and tracer (CH4 and CO) fields.Simulated SPE-induced ozone losses agree on average within 5% with the observations. Simulated NOy enhancements around 1 hPa, however, are typically 30% higher than indicated by the observations which are likely to be related to deficiencies in the used ionization rates, though other error sources related to the models' atmospheric background state and/or transport schemes cannot be excluded. The analysis of the observed and modeled NOy partitioning in the aftermath of the SPE has demonstrated the need to implement additional ion chemistry (HNO3 formation via ion-ion recombination and water cluster ions) into the chemical schemes. An overestimation of observed H2O2 enhancements by all models hints at an underestimation of the OH/HO2 ratio in the upper polar stratosphere during the SPE. The analysis of chlorine species perturbations has shown that the encountered differences between models and observations, particularly the underestimation of observed ClONO2 enhancements, are related to a smaller availability of ClO in the polar night region already before the SPE. In general, the intercomparison has demonstrated that differences in the meteorology and/or initial state of the atmosphere in the simulations cause a relevant variability of the model results, even on a short timescale of only a few days.

KW - OCTOBER-NOVEMBER 2003

KW - CHEMISTRY-CLIMATE MODEL

KW - MIDDLE ATMOSPHERE

KW - MICHELSON INTERFEROMETER

KW - SOUNDING MIPAS

KW - OZONE DEPLETION

KW - TECHNICAL NOTE

KW - ION CHEMISTRY

KW - HNO3

KW - VALIDATION

U2 - 10.5194/acp-11-9089-2011

DO - 10.5194/acp-11-9089-2011

M3 - статья

VL - 11

SP - 9089

EP - 9139

JO - Atmospheric Chemistry and Physics

JF - Atmospheric Chemistry and Physics

SN - 1680-7316

IS - 17

ER -

ID: 117040260