The tropospheric vertical column concentration (VCDtrop) of NO2, SO2, and HCHO was retrieved, respectively, by employing the geometric method (Geomtry), simplified model method (Model), and look-up table method (Table) with the observation spectra of the multi-axis differential absorption spectroscopy instrument (MAX-DOAS). The correlation and relative differences of the inversion results obtained by these three algorithms, as well as the changes in quantiles, were explored. The comparative analysis reveals that the more concentrated the vertical distribution height of gas components is in the near-surface layer, the better the conformity of the VCDtrop retrieved by different algorithms. However, the increase in relative differences is also related to the diurnal variation of gas components. The influence of aerosols on the inversion of the VCDtrop is greater than the change in the vertical distribution height of the gas component itself. The near-surface concentration and distribution height of gas components are the internal factors that give rise to relative differences in the inversion of the VCDtrop by different algorithms, while aerosols are one of the extremely important external reasons. The VCDtrop inverted by Geomtry without considering the influence of aerosols is generally larger except for NO2. Model sets up aerosols in accordance with the height and meteorological conditions of the atmospheric environment. Table can invert the aerosol profile in real time. Compared with Model, it shows a significant improvement in the refined setting of aerosols. Moreover, while obtaining the vertical distribution of aerosols, it can invert the diurnal variation of the VCDtrop. The VCDtrop inverted by Table is the smallest, and the relative difference with Model is on average about 10% smaller. The relative difference of the VCDtrop for the same height (aerosol optical thickness) quantile is 7–15% (about 25% lower on average). When comparing the inversion results of Table with the Ozone Monitoring Instrument (OMI) satellite product, the MAX-DOAS inversion results of NO2, SO2, and HCHO are all larger than the OMI product. This is related to the different observation methods of the MAX-DOAS and OMI and the configuration between the aerosol layer and the distribution height of gas components.
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