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A joint effort to deliver satellite retrieved atmospheric CO2 concentrations for surface flux inversions: The ensemble median algorithm EMMA

  • M. Reuter
  • , H. Bösch
  • , H. Bovensmann
  • , A. Bril
  • , M. Buchwitz
  • , A. Butz
  • , J. P. Burrows
  • , C. W. O'Dell
  • , S. Guerlet
  • , O. Hasekamp
  • , J. Heymann
  • , N. Kikuchi
  • , S. Oshchepkov
  • , R. Parker
  • , S. Pfeifer
  • , O. Schneising
  • , T. Yokota
  • , Y. Yoshida
  • University of Bremen
  • University of Leicester
  • National Institute for Environmental Studies of Japan
  • Institute of Meteorology and Climate Research
  • Cooperative Institute for Research in the Atmosphere
  • SRON - Netherlands Institute for Space Research
  • Helmholtz-Zentrum Hereon GmbH

Résultats de recherche: Contribution à un journalArticleRevue par des pairs

Résumé

We analyze an ensemble of seven XCO2 retrieval algorithms for SCIAMACHY (scanning imaging absorption spectrometer of atmospheric chartography) and GOSAT (greenhouse gases observing satellite). The ensemble spread can be interpreted as regional uncertainty and can help to identify locations for new TCCON (total carbon column observing network) validation sites. Additionally, we introduce the ensemble median algorithm EMMA combining individual soundings of the seven algorithms into one new data set. The ensemble takes advantage of the algorithms' independent developments. We find ensemble spreads being often < 1 ppm but rising up to 2 ppm especially in the tropics and East Asia. On the basis of gridded monthly averages, we compare EMMA and all individual algorithms with TCCON and CarbonTracker model results (potential outliers, north/south gradient, seasonal (peak-to-peak) amplitude, standard deviation of the difference). Our findings show that EMMA is a promising candidate for inverse modeling studies. Compared to CarbonTracker, the satellite retrievals find consistently larger north/south gradients (by 0.3-0.9 ppm) and seasonal amplitudes (by 1.5-2.0 ppm).

langue originaleAnglais
Pages (de - à)1771-1780
Nombre de pages10
journalAtmospheric Chemistry and Physics
Volume13
Numéro de publication4
Les DOIs
étatPublié - 4 mars 2013
Modification externeOui

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