scholarly journals Evaluation of tropospheric ozone columns derived from assimilated GOME ozone profile observations

2009 ◽  
Vol 9 (20) ◽  
pp. 8105-8120 ◽  
Author(s):  
A. T. J. de Laat ◽  
R. J. van der A ◽  
M. van Weele

Abstract. Tropospheric O3 column estimates are produced and evaluated from spaceborne O3 observations by the subtraction of assimilated O3 profile observations from total column observations, the so-called Tropospheric O3 ReAnalysis or TORA method. Here we apply the TORA method to six years (1996–2001) of ERS-2 GOME/TOMS total O3 and ERS-2 GOME O3 profile observations using the TM5 global chemistry-transport model with a linearized O3 photochemistry parameterization scheme. Free running TM5 simulations show good agreement with O3 sonde observations in the upper-tropospheric and lower stratospheric region (UTLS), both for short day-to-day variability as well as for monthly means. The assimilation of GOME O3 profile observations counteracts the mid-latitude stratospheric O3 drift caused by the overstrong stratospheric meridional circulation in TM5. Assimilation of GOME O3 profile observations also improves the bias and correlations in the tropical UTLS region but slightly degrades the model-to-sonde correlations and bias of extra-tropical UTLS. We suggest that this degradation is related to the large ground pixel size of the GOME O3 measurements (960×100 km) in combination with retrieval and calibration errors. The added value of the assimilation of GOME O3 profiles compared to stand-alone model simulations lays in the long term variations of stratospheric O3, not in short term synoptic variations. The evaluation of daily and monthly tropospheric O3 columns obtained from total column observations and using the TORA methodology shows that the use of GOME UV-VIS nadir O3 profiles in combination with the spatial resolution of the model does not result in satisfactory residual tropospheric ozone columns.

2009 ◽  
Vol 9 (3) ◽  
pp. 11811-11841 ◽  
Author(s):  
A. T. J. de Laat ◽  
R. J. van der A ◽  
M. van Weele

Abstract. Tropospheric O3 column estimates are produced and evaluated from spaceborne O3 observations by the subtraction of assimilated O3 profile observations from total column observations, the so-called Tropospheric O3 ReAnalysis or TORA method. Here we apply the TORA method to six years (1996–2001) of ERS-2 GOME/TOMS total O3 and ERS-2 GOME O3 profile observations using the TM5 global chemistry-transport model with a linearized O3 photochemistry parameterization scheme. Free running TM5 simulations show good agreement with O3 sonde observations in the upper-tropospheric and lower stratospheric (UTLS). Assimilation of GOME O3 profile observations improves the comparisons in the tropical UTLS region but slightly degrades the model-to-sonde comparisons in the extra-tropical UTLS for both short day-do-day variability as well as for monthly means. We suggest that this degradation is related to the large ground pixel size of the GOME O3 measurements (960×100 km) in combination with retrieval and calibration errors. The assimilation of GOME O3 profile observations does counter the gradual multiyear mid-latitude stratospheric O3 accumulation caused by the overstrong stratospheric meridional circulation in TM5. The evaluation of daily and monthly tropospheric O3 columns obtained from total column observations and using the TORA methodology shows realistic residuals within the tropics but unrealistically large deviations outside of the tropics, although average biases remain small for the monthly means. The findings of this paper suggest that improvements can be expected by using O3 observations from present-day instruments like MetOp/GOME-2 and EOS-AURA/OMI.


2014 ◽  
Vol 7 (11) ◽  
pp. 3783-3799 ◽  
Author(s):  
A. T. J. de Laat ◽  
I. Aben ◽  
M. Deeter ◽  
P. Nédélec ◽  
H. Eskes ◽  
...  

Abstract. Validation results from a comparison between Measurement Of Pollution In The Troposphere (MOPITT) V5 Near InfraRed (NIR) carbon monoxide (CO) total column measurements and Measurement of Ozone and Water Vapour on Airbus in-service Aircraft (MOZAIC)/In-Service Aircraft for a Global Observing System (IAGOS) aircraft measurements are presented. A good agreement is found between MOPITT and MOZAIC/IAGOS measurements, consistent with results from earlier studies using different validation data and despite large variability in MOPITT CO total columns along the spatial footprint of the MOZAIC/IAGOS measurements. Validation results improve when taking the large spatial footprint of the MOZAIC/IAGOS data into account. No statistically significant drift was detected in the validation results over the period 2002–2010 at global, continental and local (airport) scales. Furthermore, for those situations where MOZAIC/IAGOS measurements differed from the MOPITT a priori, the MOPITT measurements clearly outperformed the MOPITT a priori data, indicating that MOPITT NIR retrievals add value to the MOPITT a priori. Results from a high spatial resolution simulation of the chemistry-transport model MOCAGE (MOdèle de Chimie Atmosphérique à Grande Echelle) showed that the most likely explanation for the large MOPITT variability along the MOZAIC-IAGOS profile flight path is related to spatio-temporal CO variability, which should be kept in mind when using MOZAIC/IAGOS profile measurements for validating satellite nadir observations.


2015 ◽  
Vol 8 (1) ◽  
pp. 385-398 ◽  
Author(s):  
G. M. Miles ◽  
R. Siddans ◽  
B. J. Kerridge ◽  
B. G. Latter ◽  
N. A. D. Richards

Abstract. This paper describes and assesses the performance of the RAL (Rutherford Appleton Laboratory) ozone profile retrieval scheme for the Global Ozone Monitoring Experiment 2 (GOME-2) with a focus on tropospheric ozone. Developments to the scheme since its application to GOME-1 measurements are outlined. These include the approaches developed to account sufficiently for UV radiometric degradation in the Hartley band and for inadequacies in knowledge of instrumental parameters in the Huggins bands to achieve the high-precision spectral fit required to extract information on tropospheric ozone. The assessment includes a validation against ozonesondes (sondes) sampled worldwide over 2 years (2007–2008). Standard deviations of the ensemble with respect to the sondes are considerably lower for the retrieved profiles than for the a priori, with the exception of the lowest subcolumn. Once retrieval vertical smoothing (averaging kernels) has been applied to the sonde profiles there is a retrieval bias of 6% (1.5 DU) in the lower troposphere, with smaller biases in the subcolumns above. The bias in the troposphere varies with latitude. The retrieval underestimates lower tropospheric ozone in the Southern Hemisphere (SH) (15–20% or ~ 1–3 DU) and overestimates it in the Northern Hemisphere (NH) (10% or 2 DU). The ability of the retrieval to reflect the geographical distribution of lower tropospheric ozone, globally (rather than just ozonesonde launch sites) is demonstrated by comparison with the chemistry transport model TOMCAT. For a monthly mean of cloud-cleared GOME-2 pixels, a correlation of 0.66 is found between the retrieval and TOMCAT sampled accordingly, with a bias of 0.7 Dobson Units. GOME-2 estimates higher concentrations in NH pollution centres but lower ozone in the Southern Ocean and South Pacific, which is consistent with the comparison to ozonesondes.


2016 ◽  
Vol 9 (7) ◽  
pp. 3407-3427 ◽  
Author(s):  
Elpida Leventidou ◽  
Kai-Uwe Eichmann ◽  
Mark Weber ◽  
John P. Burrows

Abstract. Tropical tropospheric ozone columns are retrieved with the convective cloud differential (CCD) technique using total ozone columns and cloud parameters from different European satellite instruments. Monthly-mean tropospheric column amounts [DU] are calculated by subtracting the above-cloud ozone column from the total column. A CCD algorithm (CCD_IUP) has been developed as part of the verification algorithm developed for TROPOspheric Monitoring Instrument (TROPOMI) on Sentinel 5-precursor (S5p) mission, which was applied to GOME/ERS-2 (1995–2003), SCIAMACHY/Envisat (2002–2012), and GOME-2/MetOp-A (2007–2012) measurements. Thus a unique long-term record of monthly-mean tropical tropospheric ozone columns (20° S–20° N) from 1996 to 2012 is now available. An uncertainty estimation has been performed, resulting in a tropospheric ozone column uncertainty less than 2 DU ( < 10 %) for all instruments. The dataset has not been yet harmonised into one consistent; however, comparison between the three separate datasets (GOME/SCIAMACHY/GOME-2) shows that GOME-2 overestimates the tropical tropospheric ozone columns by about 8 DU, while SCIAMACHY and GOME are in good agreement. Validation with Southern Hemisphere ADditional OZonesondes (SHADOZ) data shows that tropospheric ozone columns from the CCD_IUP technique and collocated integrated ozonesonde profiles from the surface up to 200 hPa are in good agreement with respect to range, interannual variations, and variances. Biases within ±5 DU and root-mean-square (RMS) deviation of less than 10 DU are found for all instruments. CCD comparisons using SCIAMACHY data with tropospheric ozone columns derived from limb/nadir matching have shown that the bias and RMS deviation are within the range of the CCD_IUP comparison with the ozonesondes. The 17-year dataset can be helpful for evaluating chemistry models and performing climate change studies.


2014 ◽  
Vol 7 (6) ◽  
pp. 5251-5291
Author(s):  
A. T. J. de Laat ◽  
I. Aben ◽  
M. Deeter ◽  
P. Nédélec ◽  
H. Eskes ◽  
...  

Abstract. Validation results from a comparison between Measurement Of Pollution In The Troposphere (MOPITT) V5 Near InfraRed (NIR) Carbon Monoxide (CO) total column measurements and Measurement of Ozone and Water Vapour on Airbus in-service Aircraft (MOZAIC)/In-Service Aircraft for a Global Observing System (IAGOS) aircraft measurements are presented. A good agreement is found between MOPITT and MOZAIC/IAGOS measurements, consistent with results from earlier studies using different validation data and despite large variability in MOPITT CO total columns along the spatial footprint of the MOZAIC/IAGOS measurements. Validation results improve when taking the large spatial footprint of the MOZAIC/IAGOS data into account. No statistically significant drift was detected in the validation results over the period 2002–2010 at global, continental and local (airport) scales. Furthermore, for those situations where MOZAIC/IAGOS measurements differed from the MOPITT a priori, the MOPITT measurements clearly outperformed the MOPITT a priori data, indicating that MOPITT NIR retrievals add value to the MOPITT a priori. Results from a high spatial resolution simulation of the chemistry-transport model MOCAGE (MOdèle de Chimie Atmosphérique à Grande Echelle) showed that the most likely explanation for the large MOPITT variability along the MOZAIC-IAGOS profile flight path is related to spatio-temporal CO variability, which should be kept in mind when using MOZAIC/IAGOS profile measurements for validating satellite nadir observations.


2014 ◽  
Vol 7 (7) ◽  
pp. 7923-7962 ◽  
Author(s):  
G. M. Miles ◽  
R. Siddans ◽  
B. J. Kerridge ◽  
B. G. Latter ◽  
N. A. D. Richards

Abstract. This paper describes and assesses the performance of the RAL (Rutherford Appleton Laboratory) ozone profile retrieval scheme for the Global Ozone Monitoring Experiment 2 (GOME-2) with a~focus on tropospheric ozone. Developments to the scheme since its application to GOME-1 measurements are outlined. These include the approaches developed to account sufficiently for UV radiometric degradation in the Hartley band and for inadequacies in knowledge of instrumental parameters in the Huggins bands to achieve the high precision spectral fit required to extract information on tropospheric ozone. The assessment includes a validation against ozonesondes (sondes) sampled worldwide over two years (2007–2008). Standard deviations of the ensemble with respect to the sondes are considerably lower for the retrieved profiles than for the a priori, with the exception of the lowest sub-column. Once retrieval vertical smoothing (averaging kernels) has been applied to the sonde profiles there is a retrieval bias of 6% (1.5 DU) in the lower troposphere, with smaller biases in the sub-columns above. The bias in the troposphere varies with latitude. The retrieval underestimates lower tropospheric ozone in the Southern Hemisphere (SH) (15–20% or ~ 1–3 DU) and overestimates it in the Northern Hemisphere (NH) (10% or 2 DU). The ability of the retrieval to represent the geographical distribution of lower tropospheric ozone, globally (rather than just ozonesonde launch sites) is demonstrated through agreement with the chemistry transport model TOMCAT. For a monthly mean of cloud-cleared GOME-2 pixels, a correlation of 0.66 is found between the retrieval and TOMCAT sampled accordingly, with a bias of 0.7 Dobson Units. GOME-2 estimates higher concentrations in NH pollution centres but lower ozone in the Southern Ocean and South Pacific, which is consistent with the comparison to ozonesondes.


2016 ◽  
Author(s):  
Elpida Leventidou ◽  
Kai-Uwe Eichmann ◽  
Mark Weber ◽  
John P. Burrows

Abstract. Tropical tropospheric ozone columns are retrieved with the Convective Clouds Differential (CCD) technique using total ozone columns and cloud parameters from different European satellite instruments. Monthly mean tropospheric column amounts [DU] are calculated by subtracting the above cloud ozone column from the total column. A CCD algorithm (CCD_IUP) has been developed (as part of the verification algorithm development for TROPOMI on Sentinel 5-precursor mission) which was applied to GOME/ ERS-2 (1995-2003), SCIAMACHY/ Envisat (2002-2012), and GOME-2/ MetOpA (2007-2012) measurements. Thus a unique long-term record of monthly mean tropical tropospheric ozone columns (20°S–20°N) from 1996 to 2012 is now available. An extensive error analysis has been performed, estimating the tropospheric ozone column uncertainties being between 5 and 7 DU (25–36%). Validation with SHADOZ ozonesonde data show that tropospheric ozone columns from CCD and collocated integrated ozonesonde profiles from the surface up to 200 hPa are in good agreement with respect to range, inter-annual variations, and variances. Biases within ±5 DU and RMS errors of less than 10 DU are found. CCD comparisons using SCIAMACHY data with tropospheric ozone columns derived from Limb Nadir Matching have shown that CCD results are less noisy and correlate better with ozonesondes. The 17-year dataset can be helpful for evaluating chemistry models and performing climate change studies.


Sensors ◽  
2018 ◽  
Vol 18 (9) ◽  
pp. 2893 ◽  
Author(s):  
Willem W. Verstraeten ◽  
Klaas Folkert Boersma ◽  
John Douros ◽  
Jason E. Williams ◽  
Henk Eskes ◽  
...  

Top-down estimates of surface NOX emissions were derived for 23 European cities based on the downwind plume decay of tropospheric nitrogen dioxide (NO2) columns from the LOTOS-EUROS (Long Term Ozone Simulation-European Ozone Simulation) chemistry transport model (CTM) and from Ozone Monitoring Instrument (OMI) satellite retrievals, averaged for the summertime period (April–September) during 2013. Here we show that the top-down NOX emissions derived from LOTOS-EUROS for European urban areas agree well with the bottom-up NOX emissions from the MACC-III inventory data (R2 = 0.88) driving the CTM demonstrating the potential of this method. OMI top-down NOX emissions over the 23 European cities are generally lower compared with the MACC-III emissions and their correlation is slightly lower (R2 = 0.79). The uncertainty on the derived NO2 lifetimes and NOX emissions are on average ~55% for OMI and ~63% for LOTOS-EUROS data. The downwind NO2 plume method applied on both LOTOS-EUROS and OMI tropospheric NO2 columns allows to estimate NOX emissions from urban areas, demonstrating that this is a useful method for real-time updates of urban NOX emissions with reasonable accuracy.


2010 ◽  
Vol 10 (16) ◽  
pp. 7763-7773 ◽  
Author(s):  
X. Yang ◽  
J. A. Pyle ◽  
R. A. Cox ◽  
N. Theys ◽  
M. Van Roozendael

Abstract. In the last two decades, significant depletion of boundary layer ozone (ozone depletion events, ODEs) has been observed in both Arctic and Antarctic spring. ODEs are attributed to catalytic destruction by bromine radicals (Br plus BrO), especially during bromine explosion events (BEs), when high concentrations of BrO periodically occur. However, neither the exact source of bromine nor the mechanism for sustaining the observed high BrO concentrations is completely understood. Here, by considering the production of sea salt aerosol from snow lying on sea ice during blowing snow events and the subsequent release of bromine, we successfully simulate the BEs using a global chemistry transport model. We find that heterogeneous reactions play an important role in sustaining a high fraction of the total inorganic bromine as BrO. We also find that emissions of bromine associated with blowing snow contribute significantly to BrO at mid-latitudes. Modeled tropospheric BrO columns generally compare well with the tropospheric BrO columns retrieved from the GOME satellite instrument (Global Ozone Monitoring Experiment). The additional blowing snow bromine source, identified here, reduces modeled high latitude lower tropospheric ozone amounts by up to an average 8% in polar spring.


2019 ◽  
Vol 19 (19) ◽  
pp. 12811-12833 ◽  
Author(s):  
Renske Timmermans ◽  
Arjo Segers ◽  
Lyana Curier ◽  
Rachid Abida ◽  
Jean-Luc Attié ◽  
...  

Abstract. We present an Observing System Simulation Experiment (OSSE) dedicated to the evaluation of the added value of the Sentinel-4 and Sentinel-5P missions for tropospheric nitrogen dioxide (NO2). Sentinel-4 is a geostationary (GEO) mission covering the European continent, providing observations with high temporal resolution (hourly). Sentinel-5P is a low Earth orbit (LEO) mission providing daily observations with a global coverage. The OSSE experiment has been carefully designed, with separate models for the simulation of observations and for the assimilation experiments and with conservative estimates of the total observation uncertainties. In the experiment we simulate Sentinel-4 and Sentinel-5P tropospheric NO2 columns and surface ozone concentrations at 7 by 7 km resolution over Europe for two 3-month summer and winter periods. The synthetic observations are based on a nature run (NR) from a chemistry transport model (MOCAGE) and error estimates using instrument characteristics. We assimilate the simulated observations into a chemistry transport model (LOTOS-EUROS) independent of the NR to evaluate their impact on modelled NO2 tropospheric columns and surface concentrations. The results are compared to an operational system where only ground-based ozone observations are ingested. Both instruments have an added value to analysed NO2 columns and surface values, reflected in decreased biases and improved correlations. The Sentinel-4 NO2 observations with hourly temporal resolution benefit modelled NO2 analyses throughout the entire day where the daily Sentinel-5P NO2 observations have a slightly lower impact that lasts up to 3–6 h after overpass. The evaluated benefits may be even higher in reality as the applied error estimates were shown to be higher than actual errors in the now operational Sentinel-5P NO2 products. We show that an accurate representation of the NO2 profile is crucial for the benefit of the column observations on surface values. The results support the need for having a combination of GEO and LEO missions for NO2 analyses in view of the complementary benefits of hourly temporal resolution (GEO, Sentinel-4) and global coverage (LEO, Sentinel-5P).


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