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  • 1
    In: Atmospheric Measurement Techniques, Copernicus GmbH, Vol. 9, No. 9 ( 2016-09-06), p. 4327-4353
    Abstract: Abstract. This paper presents an extensive intercomparison and validation for the ozone (O3) product measured by the two Infrared Atmospheric Sounding Interferometers (IASIs) launched on board the MetOp-A and MetOp-B satellites in 2006 and in 2012 respectively. IASI O3 total columns and vertical profiles obtained from Fast Optimal Retrievals on Layers for IASI (FORLI) v20140922 software (running up until recently) are validated against independent observations during the period 2008–2014 on a global scale. On average for the period 2013–2014, IASI-A and IASI-B total ozone columns (TOCs) retrieved using FORLI are consistent, with IASI-B providing slightly lower values with a global difference of only 0.2 ± 0.8 %. The comparison between IASI-A and IASI-B O3 vertical profiles shows differences within ± 2 % over the entire altitude range. Global validation results for 7 years of IASI TOCs from FORLI against the Global Ozone Monitoring Experiment-2 (GOME-2) launched on board MetOp-A and Brewer–Dobson data show that, on average, IASI overestimates the ultraviolet (UV) data by 5–6 % with the largest differences found in the southern high latitudes. The comparison with UV–visible SAOZ (Système d'Analyse par Observation Zénithale) measurements shows a mean bias between IASI and SAOZ TOCs of 2–4 % in the midlatitudes and tropics and 7 % at the polar circle. Part of the discrepancies found at high latitudes can be attributed to the limited information content in the observations due to low brightness temperatures. The comparison with ozonesonde vertical profiles (limited to 30 km) shows that on average IASI with FORLI processing underestimates O3 by  ∼  5–15 % in the troposphere while it overestimates O3 by ∼  10–40 % in the stratosphere, depending on the latitude. The largest relative differences are found in the tropical tropopause region; this can be explained by the low O3 amounts leading to large relative errors. In this study, we also evaluate an updated version of FORLI-O3 retrieval software (v20151001), using look-up tables recalculated to cover a larger spectral range using the latest HITRAN spectroscopic database (HITRAN 2012) and implementing numerical corrections. The assessment of the new O3 product with the same set of observations as that used for the validation exercise shows a correction of ∼  4 % for the TOC positive bias when compared to the UV ground-based and satellite observations, bringing the overall global comparison to ∼  1–2 % on average. This improvement is mainly associated with a decrease in the retrieved O3 concentration in the middle stratosphere (above 30 hPa/25 km) as shown by the comparison with ozonesonde data.
    Type of Medium: Online Resource
    ISSN: 1867-8548
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2016
    detail.hit.zdb_id: 2505596-3
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  • 2
    In: Atmospheric Measurement Techniques, Copernicus GmbH, Vol. 11, No. 3 ( 2018-03-09), p. 1385-1402
    Abstract: Abstract. The GOME-type Total Ozone Essential Climate Variable (GTO-ECV) is a level-3 data record, which combines individual sensor products into one single cohesive record covering the 22-year period from 1995 to 2016, generated in the frame of the European Space Agency's Climate Change Initiative Phase II. It is based on level-2 total ozone data produced by the GODFIT (GOME-type Direct FITting) v4 algorithm as applied to the GOME/ERS-2, OMI/Aura, SCIAMACHY/Envisat and GOME-2/Metop-A and Metop-B observations. In this paper we examine whether GTO-ECV meets the specific requirements set by the international climate–chemistry modelling community for decadal stability long-term and short-term accuracy. In the following, we present the validation of the 2017 release of the Climate Research Data Package Total Ozone Column (CRDP TOC) at both level 2 and level 3. The inter-sensor consistency of the individual level-2 data sets has mean differences generally within 0.5 % at moderate latitudes (±50°), whereas the level-3 data sets show mean differences with respect to the OMI reference data record that span between −0.2 ± 0.9 % (for GOME-2B) and 1.0 ± 1.4 % (for SCIAMACHY). Very similar findings are reported for the level-2 validation against independent ground-based TOC observations reported by Brewer, Dobson and SAOZ instruments: the mean bias between GODFIT v4 satellite TOC and the ground instrument is well within 1.0 ± 1.0 % for all sensors, the drift per decade spans between −0.5 % and 1.0 ± 1.0 % depending on the sensor, and the peak-to-peak seasonality of the differences ranges from ∼ 1 % for GOME and OMI to  ∼ 2 % for SCIAMACHY. For the level-3 validation, our first goal was to show that the level-3 CRDP produces findings consistent with the level-2 individual sensor comparisons. We show a very good agreement with 0.5 to 2 % peak-to-peak amplitude for the monthly mean difference time series and a negligible drift per decade of the differences in the Northern Hemisphere of −0.11 ± 0.10 % decade−1 for Dobson and +0.22 ± 0.08 % decade−1 for Brewer collocations. The exceptional quality of the level-3 GTO-ECV v3 TOC record temporal stability satisfies well the requirements for the total ozone measurement decadal stability of 1–3 % and the short-term and long-term accuracy requirements of 2 and 3 %, respectively, showing a remarkable inter-sensor consistency, both in the level-2 GODFIT v4 and in the level-3 GTO-ECV v3 datasets, and thus can be used for longer-term analysis of the ozone layer, such as decadal trend studies, chemistry–climate model evaluation and data assimilation applications.
    Type of Medium: Online Resource
    ISSN: 1867-8548
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2018
    detail.hit.zdb_id: 2505596-3
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  • 3
    In: Atmospheric Measurement Techniques, Copernicus GmbH, Vol. 11, No. 4 ( 2018-04-19), p. 2239-2255
    Abstract: Abstract. In this study, the tropospheric NO2 vertical column density (VCD) over an urban site in Guangzhou megacity in China is investigated by means of MAX-DOAS measurements during a campaign from late March 2015 to mid-March 2016. A MAX-DOAS system was deployed at the Guangzhou Institute of Geochemistry of the Chinese Academy of Sciences and operated there for about 1 year, during the spring and summer months. The tropospheric NO2 VCDs retrieved by the MAX-DOAS are presented and compared with space-borne observations from GOME-2/MetOp-A, GOME-2/MetOp-B and OMI/Aura satellite sensors. The comparisons reveal good agreement between satellite and MAX-DOAS observations over Guangzhou, with correlation coefficients ranging between 0.795 for GOME-2B and 0.996 for OMI. However, the tropospheric NO2 loadings are underestimated by the satellite sensors on average by 25.1, 10.3 and 5.7 %, respectively, for OMI, GOME-2A and GOME-2B. Our results indicate that GOME-2B retrievals are closer to those of the MAX-DOAS instrument due to the lower tropospheric NO2 concentrations during the days with valid GOME-2B observations. In addition, the effect of the main coincidence criteria is investigated, namely the cloud fraction (CF), the distance (d) between the satellite pixel center and the ground-based measurement site, as well as the time period within which the MAX-DOAS data are averaged around the satellite overpass time. The effect of CF and time window criteria is more profound on the selection of OMI overpass data, probably due to its smaller pixel size. The available data pairs are reduced to half and about one-third for CF  ≤  0.3 and CF  ≤  0.2, respectively, while, compared to larger CF thresholds, the correlation coefficient is improved to 0.996 from about 0.86, the slope value is very close to unity ( ∼  0.98) and the mean satellite underestimation is reduced to about half (from  ∼  7 to  ∼  3.5  ×  1015 molecules cm−2). On the other hand, the distance criterion affects mostly GOME-2B data selection, because GOME-2B pixels are quite evenly distributed among the different radii used in the sensitivity test. More specifically, the number of collocations is notably reduced when stricter radius limits are applied, the r value is improved from 0.795 (d ≤  50 km) to 0.953 (d ≤  20 km), and the absolute mean bias decreases about 6 times for d ≤  30 km compared to the reference case (d ≤  50 km).
    Type of Medium: Online Resource
    ISSN: 1867-8548
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2018
    detail.hit.zdb_id: 2505596-3
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  • 4
    In: Atmospheric Chemistry and Physics, Copernicus GmbH, Vol. 17, No. 9 ( 2017-05-11), p. 5829-5849
    Abstract: Abstract. One of the main issues arising from the comparison of ground-based and satellite measurements is the difference in spatial representativeness, which for locations with inhomogeneous spatial distribution of pollutants may lead to significant differences between the two data sets. In order to investigate the spatial variability of tropospheric NO2 within a sub-satellite pixel, a campaign which lasted for about 6 months was held in the greater area of Thessaloniki, Greece. Three multi-axial differential optical absorption spectroscopy (MAX-DOAS) systems performed measurements of tropospheric NO2 columns at different sites representative of urban, suburban and rural conditions. The direct comparison of these ground-based measurements with corresponding products from the Ozone Monitoring Instrument onboard NASA's Aura satellite (OMI/Aura) showed good agreement over the rural and suburban areas, while the comparison with the Global Ozone Monitoring Experiment-2 (GOME-2) onboard EUMETSAT's Meteorological Operational satellites' (MetOp-A and MetOp-B) observations is good only over the rural area. GOME-2A and GOME-2B sensors show an average underestimation of tropospheric NO2 over the urban area of about 10.51 ± 8.32  ×  1015 and 10.21 ± 8.87  × 1015 molecules cm−2, respectively. The mean difference between ground-based and OMI observations is significantly lower (6.60 ± 5.71  ×  1015 molecules cm−2). The differences found in the comparisons of MAX-DOAS data with the different satellite sensors can be attributed to the higher spatial resolution of OMI, as well as the different overpass times and NO2 retrieval algorithms of the satellites. OMI data were adjusted using factors calculated by an air quality modeling tool, consisting of the Weather Research and Forecasting (WRF) mesoscale meteorological model and the Comprehensive Air Quality Model with Extensions (CAMx) multiscale photochemical transport model. This approach resulted in significant improvement of the comparisons over the urban monitoring site. The average difference of OMI observations from MAX-DOAS measurements was reduced to −1.68 ± 5.01  ×  1015 molecules cm−2.
    Type of Medium: Online Resource
    ISSN: 1680-7324
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2017
    detail.hit.zdb_id: 2092549-9
    detail.hit.zdb_id: 2069847-1
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  • 5
    Online Resource
    Online Resource
    Copernicus GmbH ; 2018
    In:  Atmospheric Measurement Techniques Vol. 11, No. 3 ( 2018-03-29), p. 1817-1832
    In: Atmospheric Measurement Techniques, Copernicus GmbH, Vol. 11, No. 3 ( 2018-03-29), p. 1817-1832
    Abstract: Abstract. The main aim of this paper is to update existing sulfur dioxide (SO2) emission inventories over China using modern inversion techniques, state-of-the-art chemistry transport modelling (CTM) and satellite observations of SO2. Within the framework of the EU Seventh Framework Programme (FP7) MarcoPolo (Monitoring and Assessment of Regional air quality in China using space Observations) project, a new SO2 emission inventory over China was calculated using the CHIMERE v2013b CTM simulations, 10 years of Ozone Monitoring Instrument (OMI)/Aura total SO2 columns and the pre-existing Multi-resolution Emission Inventory for China (MEIC v1.2). It is shown that including satellite observations in the calculations increases the current bottom-up MEIC inventory emissions for the entire domain studied (15–55° N, 102–132° E) from 26.30 to 32.60 Tg annum−1, with positive updates which are stronger in winter ( ∼  36 % increase). New source areas were identified in the southwest (25–35° N, 100–110° E) as well as in the northeast (40–50° N, 120–130° E) of the domain studied as high SO2 levels were observed by OMI, resulting in increased emissions in the a posteriori inventory that do not appear in the original MEIC v1.2 dataset. Comparisons with the independent Emissions Database for Global Atmospheric Research, EDGAR v4.3.1, show a satisfying agreement since the EDGAR 2010 bottom-up database provides 33.30 Tg annum−1 of SO2 emissions. When studying the entire OMI/Aura time period (2005 to 2015), it was shown that the SO2 emissions remain nearly constant before the year 2010, with a drift of −0.51 ± 0.38 Tg annum−1, and show a statistically significant decline after the year 2010 of −1.64 ± 0.37 Tg annum−1 for the entire domain. Similar findings were obtained when focusing on the greater Beijing area (30–40° N, 110–120° E) with pre-2010 drifts of −0.17 ± 0.14 and post-2010 drifts of −0.47 ± 0.12 Tg annum−1. The new SO2 emission inventory is publicly available and forms part of the official EU MarcoPolo emission inventory over China, which also includes updated NOx, volatile organic compounds and particulate matter emissions.
    Type of Medium: Online Resource
    ISSN: 1867-8548
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2018
    detail.hit.zdb_id: 2505596-3
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