14 research outputs found

    New Era of Air Quality Monitoring from Space: Geostationary Environment Monitoring Spectrometer (GEMS)

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    GEMS will monitor air quality over Asia at unprecedented spatial and temporal resolution from GEO for the first time, providing column measurements of aerosol, ozone and their precursors (nitrogen dioxide, sulfur dioxide and formaldehyde). Geostationary Environment Monitoring Spectrometer (GEMS) is scheduled for launch in late 2019 - early 2020 to monitor Air Quality (AQ) at an unprecedented spatial and temporal resolution from a Geostationary Earth Orbit (GEO) for the first time. With the development of UV-visible spectrometers at sub-nm spectral resolution and sophisticated retrieval algorithms, estimates of the column amounts of atmospheric pollutants (O3, NO2, SO2, HCHO, CHOCHO and aerosols) can be obtained. To date, all the UV-visible satellite missions monitoring air quality have been in Low Earth orbit (LEO), allowing one to two observations per day. With UV-visible instruments on GEO platforms, the diurnal variations of these pollutants can now be determined. Details of the GEMS mission are presented, including instrumentation, scientific algorithms, predicted performance, and applications for air quality forecasts through data assimilation. GEMS will be onboard the GEO-KOMPSAT-2 satellite series, which also hosts the Advanced Meteorological Imager (AMI) and Geostationary Ocean Color Imager (GOCI)-2. These three instruments will provide synergistic science products to better understand air quality, meteorology, the long-range transport of air pollutants, emission source distributions, and chemical processes. Faster sampling rates at higher spatial resolution will increase the probability of finding cloud-free pixels, leading to more observations of aerosols and trace gases than is possible from LEO. GEMS will be joined by NASA's TEMPO and ESA's Sentinel-4 to form a GEO AQ satellite constellation in early 2020s, coordinated by the Committee on Earth Observation Satellites (CEOS)

    On the consistency of methane isotopologue retrievals using TCCON and multiple spectroscopic databases

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    The next and current generations of methane-retrieving satellite instruments are reliant on the Total Carbon Column Observing Network (TCCON) for validation. Understanding the biases inherent in TCCON and satellite methane retrievals is as important now as when TCCON started in 2004. In this study we highlight possible biases between different methane products by assessing the retrievals of the main methane isotopologue 12CH4. Using the TCCON GGG2014 retrieval environment, retrievals are performed using five separate spectroscopic databases from four separate TCCON sites (namely, Ascension Island, Ny-Ålesund, Darwin and Tsukuba) over the course of a year. The spectroscopic databases include those native to TCCON, GGG2014 and GGG2020; the high-resolution transmission molecular absorption database 2016 (HITRAN2016); the Gestion et Etude des Informations Spectroscopiques AtmosphĂ©riques 2020 (GEISA2020) database; and the ESA Scientific Exploitation of Operational Missions - Improved Atmospheric Spectroscopy Databases (SEOM-IAS). We assess the biases in retrieving methane using the standard TCCON windows and the methane window used by the Sentinel-5 Precursor (S5P) TROPOspheric Ozone Monitoring Instrument (TROPOMI) for each of the different spectroscopic databases. By assessing the retrieved 12CH4 values from individual windows against the standard TCCON retrievals, we find bias values of between 0.05 and 2.5 times the retrieval noise limit. These values vary depending on the window and TCCON site, with Ascension Island showing the lowest biases (typically \u3c0.5) and Ny-Ålesund or Tsukuba showing the largest. For the spectroscopic databases, GEISA2020 shows the largest biases, often greater than 1.5 across the TCCON sites and considered windows. The TROPOMI spectral window (4190-4340gcm-1) shows the largest biases of all the spectral windows, typically \u3e1, for all spectroscopic databases, suggesting that further improvements in spectroscopic parameters are necessary. We further assess the sensitivity of these biases to locally changing atmospheric conditions such as the solar zenith angle (SZA), water vapour and temperature. We find evidence of significant non-linear relationships between the variation in local conditions and the retrieval biases based on regression analysis. In general, each site, database and window combination indicates different degrees of sensitivity, with GEISA2020 often showing the most sensitivity for all TCCON sites. Ny-Ålesund and Tsukuba show the most sensitivity to variations in local condition, while Ascension Island indicates limited sensitivity. Finally, we investigate the biases associated with retrieving 13CH4 from each TCCON site and spectroscopic database, through the calculation of ÎŽ13C values. We find high levels of inconsistency, in some cases \u3e100g‰ between databases, suggesting more work is required to refine the spectroscopic parameters of 13CH4

    Impact of 3D cloud structures on the atmospheric trace gas products from UV–Vis sounders – Part 3: Bias estimate using synthetic and observational data

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    Three-dimensional (3D) cloud structures may impact atmospheric trace gas products from ultraviolet–visible (UV–Vis) sounders. We used synthetic and observational data to identify and quantify possible cloud-related bias in NO2 tropospheric vertical column density (TVCD). The synthetic data were based on high-resolution large eddy simulations which were input to a 3D radiative transfer model. The simulated visible spectra for low-earth-orbiting and geostationary geometries were analysed with standard retrieval methods and cloud correction schemes that are employed in operational NO2 satellite products. For the observational data, the NO2 products from the TROPOspheric Monitoring Instrument (TROPOMI) were used, while the Visible Infrared Imaging Radiometer Suite (VIIRS) provided high-spatial-resolution cloud and radiance data. NO2 profile shape, cloud shadow fraction, cloud top height, cloud optical depth, and solar zenith and viewing angles were identified as the metrics being the most important in identifying 3D cloud impacts on NO2 TVCD retrievals. For a solar zenith angle less than about 40∘ the synthetic data show that the NO2 TVCD bias is typically below 10 %, while for larger solar zenith angles the NO2 TVCD is low-biased by tens of percent. The horizontal variability of NO2 and differences in TROPOMI and VIIRS overpass times make it challenging to identify a similar bias in the observational data. However, for optically thick clouds above 3000 m, a low bias appears to be present in the observational data

    Impact of 3D cloud structures on the atmospheric trace gas products from UV–Vis sounders – Part 1: Synthetic dataset for validation of trace gas retrieval algorithms

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    Retrievals of trace gas concentrations from satellite observations are mostly performed for clear regions or regions with low cloud coverage. However, even fully clear pixels can be affected by clouds in the vicinity, either by shadowing or by scattering of radiation from clouds in the clear region. Quantifying the error of retrieved trace gas concentrations due to cloud scattering is a difficult task. One possibility is to generate synthetic data by three-dimensional (3D) radiative transfer simulations using realistic 3D atmospheric input data, including 3D cloud structures. Retrieval algorithms may be applied on the synthetic data, and comparison to the known input trace gas concentrations yields the retrieval error due to cloud scattering. In this paper we present a comprehensive synthetic dataset which has been generated using the Monte Carlo radiative transfer model MYSTIC (Monte Carlo code for the phYSically correct Tracing of photons In Cloudy atmospheres). The dataset includes simulated spectra in two spectral ranges (400–500 nm and the O2A-band from 755–775 nm). Moreover it includes layer air mass factors (layer-AMFs) calculated at 460 nm. All simulations are performed for a fixed background atmosphere for various sun positions, viewing directions and surface albedos. Two cloud setups are considered: the first includes simple box clouds with various geometrical and optical thicknesses. This can be used to systematically investigate the sensitivity of the retrieval error on solar zenith angle, surface albedo and cloud parameters. Corresponding 1D simulations are also provided. The second includes realistic three-dimensional clouds from an ICON large eddy simulation (LES) for a region covering Germany and parts of surrounding countries. The scene includes cloud types typical of central Europe such as shallow cumulus, convective cloud cells, cirrus and stratocumulus. This large dataset can be used to quantify the trace gas concentration retrieval error statistically. Along with the dataset, the impact of horizontal photon transport on reflectance spectra and layer-AMFs is analysed for the box-cloud scenarios. Moreover, the impact of 3D cloud scattering on the NO2 vertical column density (VCD) retrieval is presented for a specific LES case. We find that the retrieval error is largest in cloud shadow regions, where the NO2 VCD is underestimated by more than 20 %. The dataset is available for the scientific community to assess the behaviour of trace gas retrieval algorithms and cloud correction schemes in cloud conditions with 3D structure

    Impact of 3D cloud structures on the atmospheric trace gas products from UV–Vis sounders – Part 2: Impact on NO2 retrieval and mitigation strategies

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    Operational retrievals of tropospheric trace gases from space-borne spectrometers are based on one-dimensional radiative transfer models. To minimize cloud effects, trace gas retrievals generally implement a simple cloud model based on radiometric cloud fraction estimates and photon path length corrections. The latter relies on measurements of the oxygen collision pair (O2–O2) absorption at 477 nm or on the oxygen A-band around 760 nm to determine an effective cloud height. In reality however, the impact of clouds is much more complex, involving unresolved sub-pixel clouds, scattering of clouds in neighbouring pixels, and cloud shadow effects, such that unresolved three-dimensional effects due to clouds may introduce significant biases in trace gas retrievals. Although clouds have significant effects on trace gas retrievals, the current cloud correction schemes are based on a simple cloud model, and the retrieved cloud parameters must be interpreted as effective values. Consequently, it is difficult to assess the accuracy of the cloud correction only based on analysis of the accuracy of the cloud retrievals, and this study focuses solely on the impact of the 3D cloud structures on the trace gas retrievals. In order to quantify this impact, we study NO2 as a trace gas example and apply standard retrieval methods including approximate cloud corrections to synthetic data generated by the state-of-the-art three-dimensional Monte Carlo radiative transfer model MYSTIC. A sensitivity study is performed for simulations including a box cloud, and the dependency on various parameters is investigated. The most significant bias is found for cloud shadow effects under polluted conditions. Biases depend strongly on cloud shadow fraction, NO2 profile, cloud optical thickness, solar zenith angle, and surface albedo. Several approaches to correct NO2 retrievals under cloud shadow conditions are explored. We find that air mass factors calculated using fitted surface albedo or corrected using the O2–O2 slant column density can partly mitigate cloud shadow effects. However, these approaches are limited to cloud-free pixels affected by surrounding clouds. A parameterization approach is presented based on relationships derived from the sensitivity study. This allows measurements to be identified for which the standard NO2 retrieval produces a significant bias and therefore provides a way to improve the current data flagging approach

    Retrieval of Aerosol Properties

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    International audienceAtmospheric aerosol is a suspension of liquid and solid particles in air, i.e. the aerosol includes both particles and its surrounding medium; in practice aerosol is usually referred to as the suspended matter, i.e. the particles or the droplets, depending on their aggregation state
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