Validation of SO2 retrievals from the Ozone Monitoring Instrument (OMI) over NE China

The Ozone Monitoring Instrument (OMI) launched on the NASA Aura satellite in July 2004 offers unprecedented spatial resolution, coupled with contiguous daily global coverage, for space-based UV measurements of sulfur dioxide (SO2). We present a first validation of the OMI SO2 data with in-situ aircraft measurements in NE China in April 2005. The study demonstrates that OMI can distinguish between background SO2 conditions and heavy pollution on a daily basis. The noise (expressed as the standard deviation, σ) in the PBL SO2 data is ~1.5DU (Dobson Unit, 2.691016 molecules/cm2) for instantaneous field of view (IFOV) data. By looking at the pristine South Pacific under optimal conditions we have determined that temporal and spatial averaging can improve the resolution of the instrument to σ ~ 0.3 DU; the long term average over this remote location was within 0.1 DU of zero. Under polluted conditions, however, Collection 2 data are higher than aircraft measurements by a factor of two in most cases. Parameterization of the airmass factor (AMF) appears to enhance the accuracy of the SO2 data. Improved calibrations of the radiance and irradiance data (Collection 3) result in better agreement with aircraft measurements on polluted days. The re-processed and AMF-corrected Collection 3 data still show positive bias and sensitivity to UV absorbing aerosols. The difference between the in situ data and the OMI daily PBL SO2 measurements within 30 km of the aircraft profiles was about 1 DU, equivalent to ~5 ppb from 0 to 3000 m altitude. Quantifying the SO2 profile and spectral dependence of aerosol absorption between 310 and 330 nm are critical for accurate estimates of SO2 from satellite UV measurements

TROPOMI–Sentinel-5 Precursor formaldehyde validation using an extensive network of ground-based Fourier-transform infrared stations

TROPOMI (the TROPOspheric Monitoring Instrument), on board the Sentinel-5 Precursor (S5P) satellite, has been monitoring the Earth\u27s atmosphere since October 2017 with an unprecedented horizontal resolution (initially 7 km$^{2}$×3.5 km$^{2}$, upgraded to 5.5 km$^{2}$×3.5 km$^{2}$ in August 2019). Monitoring air quality is one of the main objectives of TROPOMI; it obtains measurements of important pollutants such as nitrogen dioxide, carbon monoxide, and formaldehyde (HCHO). In this paper we assess the quality of the latest HCHO TROPOMI products versions 1.1.(5-7), using ground-based solar-absorption FTIR (Fourier-transform infrared) measurements of HCHO from 25 stations around the world, including high-, mid-, and low-latitude sites. Most of these stations are part of the Network for the Detection of Atmospheric Composition Change (NDACC), and they provide a wide range of observation conditions, from very clean remote sites to those with high HCHO levels from anthropogenic or biogenic emissions. The ground-based HCHO retrieval settings have been optimized and harmonized at all the stations, ensuring a consistent validation among the sites. In this validation work, we first assess the accuracy of TROPOMI HCHO tropospheric columns using the median of the relative differences between TROPOMI and FTIR ground-based data (BIAS). The pre-launch accuracy requirements of TROPOMI HCHO are 40 %–80 %. We observe that these requirements are well reached, with the BIAS found below 80 % at all the sites and below 40 % at 20 of the 25 sites. The provided TROPOMI systematic uncertainties are well in agreement with the observed biases at most of the stations except for the highest-HCHO-level site, where it is found to be underestimated. We find that while the BIAS has no latitudinal dependence, it is dependent on the HCHO concentration levels: an overestimation (+26±5 %) of TROPOMI is observed for very low HCHO levels (8.0×10$^{15}$ molec. cm$^{-2}$). This demonstrates the great value of such a harmonized network covering a wide range of concentration levels, the sites with high HCHO concentrations being crucial for the determination of the satellite bias in the regions of emissions and the clean sites allowing a small TROPOMI offset to be determined. The wide range of sampled HCHO levels within the network allows the robust determination of the significant constant and proportional TROPOMI HCHO biases (TROPOMI =+1.10±0.05 ×10$^{15}$+0.64±0.03 × FTIR; in molecules per square centimetre). Second, the precision of TROPOMI HCHO data is estimated by the median absolute deviation (MAD) of the relative differences between TROPOMI and FTIR ground-based data. The clean sites are especially useful for minimizing a possible additional collocation error. The precision requirement of 1.2×10$^{16}$ molec. cm$^{-2}$ for a single pixel is reached at most of the clean sites, where it is found that the TROPOMI precision can even be 2 times better (0.5–0.8×10$^{15}$ molec. cm$^{-2}$ for a single pixel). However, we find that the provided TROPOMI random uncertainties may be underestimated by a factor of 1.6 (for clean sites) to 2.3 (for high HCHO levels). The correlation is very good between TROPOMI and FTIR data (R=0.88 for 3 h mean coincidences; R=0.91 for monthly means coincidences). Using about 17 months of data (from May 2018 to September 2019), we show that the TROPOMI seasonal variability is in very good agreement at all of the FTIR sites. The FTIR network demonstrates the very good quality of the TROPOMI HCHO products, which is well within the pre-launch requirements for both accuracy and precision. This paper makes suggestions for the refinement of the TROPOMI random uncertainty budget and TROPOMI quality assurance values for a better filtering of the remaining outliers

Glyoxal tropospheric column retrievals from TROPOMI – multi-satellite intercomparison and ground-based validation

We present the first global glyoxal (CHOCHO) tropospheric column product derived from the TROPOspheric Monitoring Instrument (TROPOMI) on board the Sentinel-5 Precursor satellite. Atmospheric glyoxal results from the oxidation of other non-methane volatile organic compounds (NMVOCs) and from direct emissions caused by combustion processes. Therefore, this product is a useful indicator of VOC emissions. It is generated with an improved version of the BIRA-IASB scientific retrieval algorithm relying on the differential optical absorption spectroscopy (DOAS) approach. Among the algorithmic updates, the DOAS fit now includes corrections to mitigate the impact of spectral misfits caused by scene brightness inhomogeneity and strong NO2 absorption. The product comes along with a full error characterization, which allows for providing random and systematic error estimates for every observation. Systematic errors are typically in the range of 1 ×10^14–3 ×10^14 molec. cm−2 (∼30 %–70 % in emission regimes) and originate mostly from a priori data uncertainties and spectral interferences with other absorbing species. The latter may be at the origin, at least partly, of an enhanced glyoxal signal over equatorial oceans, and further investigation is needed to mitigate them. Random errors are large ( molec. cm−2) but can be reduced by averaging observations in space and/or time. Benefiting from a high signal-to-noise ratio and a large number of small-size observations, TROPOMI provides glyoxal tropospheric column fields with an unprecedented level of detail. Using the same retrieval algorithmic baseline, glyoxal column data sets are also generated from the Ozone Monitoring Instrument (OMI) on Aura and from the Global Ozone Monitoring Experiment-2 (GOME-2) on board Metop-A and Metop-B. Those four data sets are intercompared over large-scale regions worldwide and show a high level of consistency. The satellite glyoxal columns are also compared to glyoxal columns retrieved from ground-based Multi-AXis DOAS (MAX-DOAS) instruments at nine stations in Asia and Europe. In general, the satellite and MAX-DOAS instruments provide consistent glyoxal columns both in terms of absolute values and variability. Correlation coefficients between TROPOMI and MAX-DOAS glyoxal columns range between 0.61 and 0.87. The correlation is only poorer at one mid-latitude station, where satellite data appear to be biased low during wintertime. The mean absolute glyoxal columns from satellite and MAX-DOAS generally agree well for low/moderate columns with differences of less than 1×10^14 molec. cm−2. A larger bias is identified at two sites where the MAX-DOAS columns are very large. Despite this systematic bias, the consistency of the satellite and MAX-DOAS glyoxal seasonal variability is high

Validation of methane and carbon monoxide from Sentinel-5 Precursor using TCCON and NDACC-IRWG stations

The Sentinel-5 Precursor (S5P) mission with the TROPOspheric Monitoring Instrument (TROPOMI) on board has been measuring solar radiation backscattered by the Earth\u27s atmosphere and surface since its launch on 13 October 2017. In this paper, we present for the first time the S5P operational methane (CH4) and carbon monoxide (CO) products\u27 validation results covering a period of about 3 years using global Total Carbon Column Observing Network (TCCON) and Infrared Working Group of the Network for the Detection of Atmospheric Composition Change (NDACC-IRWG) network data, accounting for a priori alignment and smoothing uncertainties in the validation, and testing the sensitivity of validation results towards the application of advanced co-location criteria. We found that the S5P standard and bias-corrected CH4 data over land surface for the recommended quality filtering fulfil the mission requirements. The systematic difference of the bias-corrected total column-averaged dry air mole fraction of methane (XCH4) data with respect to TCCON data is −0.26±0.56 % in comparison to −0.68±0.74 % for the standard XCH4 data, with a correlation of 0.6 for most stations. The bias shows a seasonal dependence. We found that the S5P CO data over all surfaces for the recommended quality filtering generally fulfil the missions requirements, with a few exceptions, which are mostly due to co-location mismatches and limited availability of data. The systematic difference between the S5P total column-averaged dry air mole fraction of carbon monoxide (XCO) and the TCCON data is on average 9.22±3.45 % (standard TCCON XCO) and 2.45±3.38 % (unscaled TCCON XCO). We found that the systematic difference between the S5P CO column and NDACC CO column (excluding two outlier stations) is on average 6.5±3.54 %. We found a correlation of above 0.9 for most TCCON and NDACC stations. The study shows the high quality of S5P CH4 and CO data by validating the products against reference global TCCON and NDACC stations covering a wide range of latitudinal bands, atmospheric conditions and surface conditions

The Spatial–Temporal Variation of Tropospheric NO2 over China during 2005 to 2018

In recent years, new and strict air quality regulations have been implemented in China. Therefore, it is of great significance to evaluate the current air pollution situation and effectiveness of actions. In this study, Ozone Monitoring Instrument (OMI) satellite data were used to detect the spatiotemporal characteristics of tropospheric NO2 columns over China from 2005 to 2018, including spatial distribution, seasonal cycles and long-term trends. The averaged NO2 pollution is higher in southeastern China and lower in the northwest, which are well delineated by the Heihe–Tengchong line. Furthermore, the NO2 loadings are highest in the North China Plain, with vertical column density (VCD) exceeding 13 × 1015 molec cm−2. Regarding the seasonal cycle, the NO2 loadings in eastern China is highest in winter and lowest in summer, while the western region shows the opposite feature. The amplitude of annual range increase gradually from the south to the north. If the entire period of 2005–2018 is taken into account, China has experienced little change in NO2. In fact, however, there appears to be significant trends of an increase followed by a downward tendency, with the turning point in the year 2012. In the former episode of 2005–2012, increasing trends overwhelm nearly the whole nation, especially in the Jing–Jin–Tang region, Shandong Province, and Northern Henan and Southern Hebei combined regions, where the rising rates were as high as 1.0–1.8 × 1015 molec cm−2 year−1. In contrast, the latter episode of 2013–2018 features remarkable declines in NO2 columns over China. Particularly, the regions where the decreased degree was remarkable in 2013–2018 were consistent with the regions where the upward trend was obvious in 2005–2012. Overall, this upward–downward pattern is true for most parts of China. However, some of the largest metropolises, such as Beijing, Shanghai and Guangzhou, witnessed a continuous decrease in the NO2 amounts, indicating earlier and more stringent measures adopted in these areas. Finally, it can be concluded that China’s recent efforts to cut NO2 pollution are successful, especially in mega cities