scholarly journals Intercomparison of daytime stratospheric NO<sub>2</sub> satellite retrievals and model simulations

2014 ◽  
Vol 7 (7) ◽  
pp. 2203-2225 ◽  
Author(s):  
M. Belmonte Rivas ◽  
P. Veefkind ◽  
F. Boersma ◽  
P. Levelt ◽  
H. Eskes ◽  
...  

Abstract. This paper evaluates the agreement between stratospheric NO2 retrievals from infrared limb sounders (Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) and High Resolution Dynamics Limb Sounder (HIRDLS)) and solar UV/VIS backscatter sensors (Ozone Monitoring Instrument (OMI), Scanning Imaging Absorption Spectrometer for Atmospheric Cartography (SCIAMACHY) limb and nadir) over the 2005–2007 period and across the seasons. The observational agreement is contrasted with the representation of NO2 profiles in 3-D chemical transport models such as the Whole Atmosphere Community Climate Model (WACCM) and TM4. A conclusion central to this work is that the definition of a reference for stratospheric NO2 columns formed by consistent agreement among SCIAMACHY, MIPAS and HIRDLS limb records (all of which agree to within 0.25 × 1015 molecules cm−2 or better than 10%) allows us to draw attention to relative errors in other data sets, e.g., (1) WACCM overestimates NO2 densities in the extratropical lower stratosphere, particularly in the springtime and over northern latitudes by up to 35% relative to limb observations, and (2) there are remarkable discrepancies between stratospheric NO2 column estimates from limb and nadir techniques, with a characteristic seasonally and latitudinally dependent pattern. We find that SCIAMACHY nadir and OMI stratospheric columns show overall biases of −0.5 × 1015 molecules cm−2 (−20%) and +0.6 × 1015 molecules cm−2 (+20%) relative to limb observations, respectively. It is argued that additive biases in nadir stratospheric columns are not expected to affect tropospheric retrievals significantly, and that they can be attributed to errors in the total slant column density, related either to algorithmic or instrumental effects. In order to obtain accurate and long-term time series of stratospheric NO2, an effort towards the harmonization of currently used differential optical absorption spectroscopy (DOAS) approaches to nadir retrievals becomes essential, as well as their agreement to limb and ground-based observations, particularly now that limb techniques are giving way to nadir observations as the next generation of climate and air quality monitoring instruments pushes forth.

2014 ◽  
Vol 7 (1) ◽  
pp. 895-948 ◽  
Author(s):  
M. Belmonte Rivas ◽  
P. Veefkind ◽  
F. Boersma ◽  
P. Levelt ◽  
H. Eskes ◽  
...  

Abstract. This paper evaluates the agreement between stratospheric NO2 retrievals from infrared limb sounders (MIPAS and HIRDLS) and solar UV/VIS backscatter sensors (OMI, SCIAMACHY limb and nadir) over the 2005–2007 period and across the seasons. The observational agreement is contrasted with the representation of NO2 profiles in 3-D chemical transport models such as the Whole Atmosphere Community Climate Model (SD-WACCM) and TM4. A conclusion central to this work is that the definition of a reference for stratospheric NO2 columns formed by consistent agreement among SCIAMACHY, MIPAS and HIRDLS limb records (all of which agree to within 0.25 × 1015 molecules cm−2 or better than 10%) allows us to draw attention to relative errors in other datasets, e.g.: (1) the WACCM model overestimates NO2 densities in the extratropical lower stratosphere, particularly over northern latitudes by up to 35% relative to limb observations, and (2) there are remarkable discrepancies between stratospheric NO2 column estimates from limb and nadir techniques, with a characteristic seasonal and latitude dependent pattern. We find that SCIAMACHY nadir and OMI stratospheric columns show overall biases of −0.6 × 1015 molecules cm−2 (−20%) and +0.6 × 10 15 molecules cm−2 (+20%) relative to limb observations. It is highlighted that biases in nadir stratospheric columns are not expected to affect tropospheric retrievals significantly, and that they can be attributed to errors in the total slant column density, either related to algorithmic or instrumental effects. In order to obtain accurate and long time series of stratospheric NO2, a critical evaluation of the currently used Differential Optical Absorption Spectroscopy (DOAS) approaches to nadir retrievals becomes essential, as well as their agreement to limb and ground-based observations, particularly now that limb techniques are giving way to nadir observations as the next generation of climate and air quality monitoring instruments pushes forth.


2013 ◽  
Vol 6 (4) ◽  
pp. 7811-7865 ◽  
Author(s):  
F. Ebojie ◽  
C. von Savigny ◽  
A. Ladstätter-Weißenmayer ◽  
A. Rozanov ◽  
M. Weber ◽  
...  

Abstract. Tropospheric ozone, O3, has two sources: transport from the stratosphere and photochemical production in the troposphere. It plays important roles in atmospheric chemistry and climate change. In this manuscript we describe the retrieval of tropospheric O3 columns from limb-nadir matching (LNM) observations of the SCanning Imaging Absorption spectroMeter for Atmospheric CHartographY (SCIAMACHY) instrument, which flies as part of the payload onboard the European Space Agency (ESA) satellite Envisat. This retrieval technique is a residual approach that utilizes the subtraction of the stratospheric O3 columns, derived from the limb observations, from the total O3 columns, derived from the nadir observations. The technique requires accurate knowledge of the stratospheric O3 columns, the total O3 columns, tropopause height, and their associated errors. The stratospheric O3 columns were determined from the stratospheric O3 profile retrieved in the Hartley and Chappius bands, based on SCIAMACHY limb scattering measurements. The total O3 columns were also derived from SCIAMACHY measurements, in the nadir viewing mode using the Weighting Function Differential Optical Absorption Spectroscopy (WFDOAS) technique in the Huggins band. Comparisons of the tropospheric O3 columns from SCIAMACHY and collocated measurements from ozonesondes, in both hemispheres between January 2003 and December 2011 show agreement to within 2–5 DU (1 DU = 2.69 × 1016 molecules cm−2). Comparison of tropospheric O3 from SCIAMACHY with the results from ozonesondes, the Tropospheric Emission Spectrometer (TES), and the LNM method combining Ozone Monitoring Instrument (OMI) and Microwave Limb Sounder (MLS) data (hereinafter referred to as OMI/MLS), have been investigated. We find that all four retrieved data sets show agreement within the error bars and exhibit strong seasonal variation, which differs in amplitude. The spatial distribution of tropospheric ozone observed shows pollution plumes related to the release of precursors at the different seasons in both hemispheres.


2005 ◽  
Vol 5 (7) ◽  
pp. 1835-1841 ◽  
Author(s):  
S. Noël ◽  
M. Buchwitz ◽  
H. Bovensmann ◽  
J. P. Burrows

Abstract. A first validation of water vapour total column amounts derived from measurements of the SCanning Imaging Absorption spectroMeter for Atmospheric CHartographY (SCIAMACHY) in the visible spectral region has been performed. For this purpose, SCIAMACHY water vapour data have been determined for the year 2003 using an extended version of the Differential Optical Absorption Spectroscopy (DOAS) method, called Air Mass Corrected (AMC-DOAS). The SCIAMACHY results are compared with corresponding water vapour measurements by the Special Sensor Microwave Imager (SSM/I) and with model data from the European Centre for Medium-Range Weather Forecasts (ECMWF). In confirmation of previous results it could be shown that SCIAMACHY derived water vapour columns are typically slightly lower than both SSM/I and ECMWF data, especially over ocean areas. However, these deviations are much smaller than the observed scatter of the data which is caused by the different temporal and spatial sampling and resolution of the data sets. For example, the overall difference with ECMWF data is only -0.05 g/cm2 whereas the typical scatter is in the order of 0.5 g/cm2. Both values show almost no variation over the year. In addition, first monthly means of SCIAMACHY water vapour data have been computed. The quality of these monthly means is currently limited by the availability of calibrated SCIAMACHY spectra. Nevertheless, first comparisons with ECMWF data show that SCIAMACHY (and similar instruments) are able to provide a new independent global water vapour data set.


2015 ◽  
Vol 8 (11) ◽  
pp. 11467-11511 ◽  
Author(s):  
S. Noël ◽  
K. Bramstedt ◽  
M. Hilker ◽  
P. Liebing ◽  
J. Plieninger ◽  
...  

Abstract. Stratospheric profiles of methane (CH4) and carbon dioxide (CO2) have been derived from solar occultation measurements of the SCanning Imaging Absorption spectroMeter for Atmospheric CHartographY (SCIAMACHY). The retrieval is performed using a method called "Onion Peeling DOAS" (ONPD) which combines an onion peeling approach with a weighting function DOAS (Differential Optical Absorption Spectroscopy) fit. By use of updated pointing information and optimisation of the data selection and of the retrieval approach the altitude range for reasonable CH4 could be extended to about 17 to 45 km. Furthermore, the quality of the derived CO2 has been assessed such that now the first stratospheric profiles of CO2 from SCIAMACHY are available. Comparisons with independent data sets yield an estimated accuracy of the new SCIAMACHY stratospheric profiles of about 5–10 % for CH4 and 2–3 % for CO2. The accuracy of the products is currently mainly restricted by the appearance of unexpected vertical oscillations in the derived profiles which need further investigation. Using the improved ONPD retrieval, CH4 and CO2 stratospheric data sets covering the whole SCIAMACHY time series (August 2002–April 2012) and the latitudinal range between about 50 and 70° N have been derived. Based on these time series, CH4 and CO2 trends have been estimated, which are in reasonable agreement with total column trends for these gases. This shows that the new SCIAMACHY data sets can provide valuable information about the stratosphere.


2015 ◽  
Vol 15 (7) ◽  
pp. 10085-10122 ◽  
Author(s):  
C. McLandress ◽  
T. G. Shepherd ◽  
A. I. Jonsson ◽  
T. von Clarmann ◽  
B. Funke

Abstract. A method is proposed for merging different nadir-sounding climate data records using measurements from high resolution limb sounders to provide a transfer function between the different nadir measurements. The nadir-sounding records need not be overlapping so long as the limb-sounding record bridges between them. The method is applied to global mean stratospheric temperatures from the NOAA Climate Data Records based on the Stratospheric Sounding Unit (SSU) and the Advanced Microwave Sounding Unit-A (AMSU), extending the SSU record forward in time to yield a continuous data set from 1979 to present. SSU and AMSU are bridged using temperature measurements from the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS), which is of high enough vertical resolution to accurately represent the weighting functions of both SSU and AMSU. For this application, a purely statistical approach is not viable since the different nadir channels are not sufficiently linearly independent, statistically speaking. The extended SSU global-mean data set is in good agreement with temperatures from the Microwave Limb Sounder (MLS) on the Aura satellite, with both exhibiting a cooling trend of ~ 0.6 ± 0.3 K decade−1 in the upper stratosphere from 2004–2012. The extended SSU data set also compares well with chemistry-climate model simulations over its entire record, including the contrast between the weak cooling seen over 1995–2004 compared with the large cooling seen in the period 1986–1995 of strong ozone depletion.


2014 ◽  
Vol 7 (7) ◽  
pp. 2073-2096 ◽  
Author(s):  
F. Ebojie ◽  
C. von Savigny ◽  
A. Ladstätter-Weißenmayer ◽  
A. Rozanov ◽  
M. Weber ◽  
...  

Abstract. Tropospheric ozone (O3), has two main sources: transport from the stratosphere and photochemical production in the troposphere. It plays important roles in atmospheric chemistry and climate change. Its amount and destruction are being modified by anthropogenic activity. Global measurements are needed to test our understanding of its sources and sinks. In this paper, we describe the retrieval of tropospheric O3 columns (TOCs) from the combined limb and nadir observations (hereinafter referred to as limb–nadir-matching (LNM)) of the SCanning Imaging Absorption spectroMeter for Atmospheric CHartographY (SCIAMACHY) instrument, which flew as part of the payload onboard the European Space Agency (ESA) satellite Envisat (2002–2012). The LNM technique used in this study is a residual approach that subtracts stratospheric O3 columns (SOCs), retrieved from the limb observations, from the total O3 columns (TOZs), derived from the nadir observations. The technique requires accurate knowledge of the SOCs, TOZs, tropopause height, and their associated errors. The SOCs were determined from the stratospheric O3 profiles retrieved in the Hartley and Chappuis bands from SCIAMACHY limb scattering measurements. The TOZs were also derived from SCIAMACHY measurements, but in this case from the nadir viewing mode using the Weighting Function Differential Optical Absorption Spectroscopy (WFDOAS) technique in the Huggins band. Comparisons of the TOCs from SCIAMACHY and collocated measurements from ozonesondes in both hemispheres between January 2003 and December 2011 show agreement to within 2–5 DU (1 DU = 2.69 × 1016 molecules cm−2). TOC values from SCIAMACHY have also been compared to the results from the Tropospheric Emission Spectrometer (TES) and from the LNM technique exploiting Ozone Monitoring Instrument (OMI) and Microwave Limb Sounder (MLS) data (hereinafter referred to as OMI/MLS). All compared data sets agree within the given data product error range and exhibit similar seasonal variations, which, however, differ in amplitude. The spatial distributions of tropospheric O3 in the SCIAMACHY LNM TOC product show characteristic variations related to stratosphere–troposphere exchange (STE) processes, anthropogenic activities and biospheric emissions.


2015 ◽  
Vol 8 (3) ◽  
pp. 2437-2500
Author(s):  
R. Shaiganfar ◽  
S. Beirle ◽  
H. Petetin ◽  
Q. Zhang ◽  
M. Beekmann ◽  
...  

Abstract. We compare tropospheric column densities (vertically integrated concentrations) of NO2 from three data sets for the metropolitan area of Paris during two extensive measurement campaigns (25 days in summer 2009 and 29 days in winter 2010) within the European research project MEGAPOLI. The selected data sets comprise a regional chemical transport model (CHIMERE) as well as two observational data sets: ground based mobile Multi-AXis-Differential Optical Absorption Spectroscopy (car-MAX-DOAS) measurements and satellite measurements from the Ozone Monitoring Instrument (OMI). On most days, car-MAX-DOAS measurements were carried out along large circles (diameter ~35 km) around Paris. The car-MAX-DOAS results are compared to coincident data from CHIMERE and OMI. All three data sets have their specific strengths and weaknesses, especially with respect to their spatio-temporal resolution and coverage as well as their uncertainties. Thus we compare them in two different ways: first, we simply consider the original data sets. Second, we compare modified versions making synergistic use of the complementary information from different data sets. For example, profile information from the regional model is used to improve the satellite data, observations of the horizontal trace gas distribution are used to adjust the respective spatial patterns of the model simulations, or the model is used as a transfer tool to bridge the spatial scales between car-MAX-DOAS and satellite observations. Using the modified versions of the data sets, the comparison results substantially improve compared to the original versions. In general, good agreement between the data sets is found outside the emission plume, but inside the emission plumes the tropospheric NO2 VCDs are systematically underestimated by the CHIMERE model and the satellite observations (compared to the car-MAX-DOAS observations). One major result from our study is that for satellite validation close to strong emission sources (like power plants or megacities) detailed information about the intra-pixel heterogeneity is essential. Such information may be gained from simultaneous car-MAX-DOAS measurements using multiple instruments or by combining (car-) MAX-DOAS measurements with results from regional model simulations.


2010 ◽  
Vol 10 (11) ◽  
pp. 5213-5222 ◽  
Author(s):  
J. Kar ◽  
J. Fishman ◽  
J. K. Creilson ◽  
A. Richter ◽  
J. Ziemke ◽  
...  

Abstract. In view of the proposed geostationary satellite missions to monitor air quality from space, it is important to first assess the capability of the current suite of satellite instruments to provide information on the urban scale pollution. We explore the possibility of detecting urban signatures in the tropospheric column ozone data derived from Total Ozone Mapping Spectrometer (TOMS)/Solar Backscattered Ultraviolet (SBUV) and Ozone Monitoring Instrument (OMI)/Microwave Limb Sounder (MLS) satellite data. We find that distinct isolated plumes of tropospheric ozone near several large and polluted cities around the world may be detected in these data sets. The ozone plumes generally correspond with the tropospheric column NO2 plumes around these cities as observed by the Scanning Imaging Absorption Spectrometer for Atmospheric Chartography (SCIAMACHY) instrument. Similar plumes are also seen in tropospheric mean ozone mixing ratio distribution after accounting for the surface and tropopause pressure variations. The total column ozone retrievals indicate fairly significant sensitivity to the lower troposphere over the polluted land areas, which might help explain these detections. These results indicate that ultraviolet (UV) measurements may, in principle, be able to capture the urban signatures and may have implications for future missions using geostationary satellites.


2005 ◽  
Vol 5 (2) ◽  
pp. 1925-1942 ◽  
Author(s):  
S. Noël ◽  
M. Buchwitz ◽  
H. Bovensmann ◽  
J. P. Burrows

Abstract. A first validation of water vapour total column amounts derived from measurements of the SCanning Imaging Absorption spectroMeter for Atmospheric CHartographY (SCIAMACHY) in the visible spectral region has been performed. For this purpose, SCIAMACHY water vapour data have been determined for the year 2003 using an extended version of the Differential Optical Absorption Spectroscopy (DOAS) method, called Air Mass Corrected (AMC-DOAS). The SCIAMACHY results are compared with corresponding water vapour measurements by the Special Sensor Microwave Imager (SSM/I) and with model data from the European Centre for Medium-Range Weather Forecasts (ECMWF). In confirmation of previous results it could be shown that SCIAMACHY derived water vapour columns are typically slightly lower than both SSM/I and ECMWF data, especially over ocean areas. However, these deviations are much smaller than the observed scatter of the data which is caused by the different temporal and spatial sampling and resolution of the data sets. For example, the overall difference with ECMWF data is only −0.05 g/cm2 whereas the typical scatter is in the order of 0.5 g/cm2. Both values show almost no variation over the year. In addition, first monthly means of SCIAMACHY water vapour data have been computed. The quality of these monthly means is currently limited by the availability of calibrated SCIAMACHY spectra. Nevertheless, first comparisons with ECMWF data show that SCIAMACHY (and similar instruments) are able to provide a new independent global water vapour data set.


2021 ◽  
Author(s):  
Tobias Küchler ◽  
Stefan Noël ◽  
Heinrich Bovensmann ◽  
John Philip Burrows ◽  
Thomas Wagner ◽  
...  

Abstract. Water vapour is the most abundant natural greenhouse gas in the Earth's atmosphere and global data sets are required for meteorological applications and climate research. The Tropospheric Ozone Monitoring Instrument (TROPOMI) onboard Sentinel 5 Precursor (S5P) launched on 13 October 2017 has a very high spatial resolution of around 5 km and a daily global coverage. Currently, there is no operational total water vapour product for S5P measurements. Here, we present first results of a new scientific total column water vapour (TCWV) product for S5P using the so-called Air Mass Corrected Differential Optical Absorption Spectroscopy (AMC-DOAS) scheme. This method analyses spectral data between 688 and 700 nm and has already been successfully applied to measurements from the Global Monitoring Experiment (GOME) on ERS-2, the Scanning Imaging Absorption Spectrometer for Atmospheric Chartography (SCIAMACHY) on Envisat and GOME-2 on MetOp. The adaptation of the AMC-DOAS method to S5P data especially includes an additional post-processing procedure to correct the influences of surface albedo, cloud height and cloud fraction. The quality of the new S5P AMC-DOAS water vapour product is assessed by comparisons with data from GOME-2 on MetOp-B retrieved also with the AMC-DOAS algorithm and with four completely independent data sets, namely re-analysis data from the European Centre for Medium range Weather Forecast (ECMWF ERA5), data obtained by the Special Sensor Microwave Imager and Sounder (SSMIS) flown on the Defense Meteorological Satellite Program (DMSP) platform 16 and two scientific S5P TCWV products derived from TROPOMI measurements. Both are recently published TCWV products for S5P provided by the Max Planck Institute for Chemistry (MPIC) in Mainz and the Netherlands Institute for Space Research (SRON), Utrecht. The SRON TCWV is limited to clear sky scenes over land. These comparisons reveal a good agreement between the various data sets but also some systematic deviations between all of them. On average, the derived offset between AMC-DOAS S5P TCWV and AMC-DOAS GOME-2B TCWV is negative (around −1.5 kg m−2) over land and positive over ocean surfaces (more than 1.5 kg m−2). In contrast, SSMIS TCWV is on average lower than AMC-DOAS S5P TCWV by about 3 kg m−2. TCWV from ERA5 and S5P AMC-DOAS TCWV comparison shows spatial differences over both land and water surface. Over land there are systematical spatial structures with enhanced discrepancies between S5P AMC-DOAS TCWV and ERA5 TCWV in tropical regions. Over sea, S5P AMC-DOAS TCWV is slightly lower than ERA5 TCWV by around 2 kg m−2. The S5P AMC-DOAS TCWV and S5P TCWV from MPIC agree on average within 1 kg m−2 over both land and ocean. TCWV from SRON shows differences to AMC-DOAS S5P TCWV of around 1.2 kg m−2. All of these deviations are in line with the accuracy of these products and with the typical range of deviations of 5 kg m−2 obtained when comparing different TCWV data sets. The AMC-DOAS TCWV product for S5P provides therefore a valuable new and independent data set for atmospheric applications which also shows a better spatial coverage than the other S5P TCWV products.


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