This study presents the Ozone Monitoring Instrument (OMI) Collection 4 formaldehyde (HCHO) retrieval developed with the Smithsonian Astrophysical Observatory’s (SAO) Making Earth System Data Records for Use in Research Environments (MEaSUREs) algorithm. The retrieval algorithm updates and makes improvements to the NASA operational OMI HCHO (OMI Collection 3 HCHO) algorithm, and has been transitioned to use OMI Collection 4 Level-1B radiances. This paper describes the updated retrieval algorithm and compares Collection 3 and Collection 4 data products. The OMI Collection 4 HCHO exhibits remarkably improved stability over time in comparison to the OMI Collection 3 HCHO product, with better precision and the elimination of artificial trends present in the Collection 3 during the later years of the mission. We validate the OMI Collection 4 HCHO data product using Fourier-Transform Infrared (FTIR) ground-based HCHO measurements. The climatological monthly averaged OMI Collection 4 HCHO vertical column densities (VCDs) agree well with the FTIR VCDs, with a correlation coefficient of 0.83, root-mean-square error (RMSE) of 2.98 × 1015 molecules cm-2, regression slope of 0.79, and intercept of 8.21 × 1014 molecules cm-2. Additionally, we compare the monthly averaged OMI Collection 4 HCHO VCDs to OMPS Suomi NPP, OMPS NOAA-20, and TROPOMI HCHO VCDs in overlapping years for twelve geographic regions. This comparison demonstrates high correlation coefficients of 0.98 (OMPS Suomi NPP), 0.97 (OMPS NOAA-20), and 0.90 (TROPOMI).

Temperature is the principal driver of global HCHO and its primary oxidation precursor biogenic volatile organic compounds (BVOCs). We revisit such a temperature (T-) dependency globally, leveraging TROPOMI HCHO column data. We find substantial variations in the T-dependency of biogenic HCHO across plant functional types (PFTs), with the highest over Broadleaf Evergreen Tropical Trees (doubling every 6.0 K ± 2.1 K) and lowest over Arctic C3 Grass (doubling every 30.8 K ± 9.6 K). The GEOS-Chem model interprets HCHO columns’ T-dependency at the PFT level (r = 0.87), with a 16% discrepancy on average. The discrepancy can be explained by BVOC emissions T-dependency for Broadleaf Evergreen Tropical Trees and Warm C4 Grass and can be attributed to the insensitivity of HCHO columns to BVOC emissions for other PFTs. Our findings underscore a potentially magnified variation of BVOC emissions by GEOS-Chem and MEGAN therein, particularly in regions experiencing greater temperature variations.

A document by Xiaoxing Zuo. Click on the document to view its contents.

Policies to regulate severe surface ozone pollution in cities in India are challenging to develop, due to the complex dependence on precursor emissions of volatile organic compounds (VOCs) and nitrogen oxides (NOx), non-linear chemistry leading to ozone formation, and very limited spatial and temporal surface air quality monitoring. Ratios of space-based observations of formaldehyde (HCHO), an intermediate oxidation product of VOCs, and nitrogen dioxide (NO2) have been used to characterize the sensitivity of surface ozone production to precursor emissions of VOCs and NOx, but interpretation of these depends on the local oxidation regime. Here we develop an improved approach in which we discretize the data into background HCHO due to methane and other long-lived VOCs (regression intercept) and the local relationship (regression slope) between HCHO associated with reactive VOCs and NO2. We apply this to TROPOMI HCHO and NO2 tropospheric columns oversampled to higher spatial resolution than the native pixel resolution of the instrument over the ten most populous cities in India. We use GEOS-Chem to characterize the ozone production regimes and then apply this updated interpretation of the relationship between HCHO and NO2 to the oversampled TROPOMI columns to identify the most effective strategies for regulating ozone and whether these should vary seasonally and spatially.

We describe new publicly-available, multi-year formaldehyde (HCHO) data records from the Ozone Mapping and Profiler Suite (OMPS) nadir mapper (NM) instruments on the Suomi NPP and NOAA-20 satellites. The OMPS-NM instruments measure backscattered UV light over the globe once per day, with spatial resolutions close to nadir of 50 × 50 km² (OMPS/Suomi-NPP) and 17 × 17 km² or 12 × 17 km² (OMPS/NOAA-20). After a preliminary instrument line shape and wavelength calibration using on-orbit observations, we use the backscatter measurements in a direct spectral fit of radiances, in combination with a nadir reference spectrum collected over a clean area, to determine slant columns of HCHO. The slant columns are converted to vertical columns using air mass factors derived through scene-by-scene radiative transfer calculations. Finally, a correction is applied to account for background HCHO in the reference spectrum, as well as any remaining high-latitude biases. We investigate the consistency of the OMPS products from Suomi NPP and NOAA-20 using long-term monthly means over 12 geographic regions, and also compare the products with publicly-available TROPOMI HCHO observations. OMPS/Suomi-NPP and OMPS/NOAA-20 monthly mean HCHO vertical columns are highly consistent (r = 0.98), with low proportional (2 %) and offset (2×10¹⁴ molecules cm⁻²) biases. OMPS HCHO monthly means are also well-correlated with those from TROPOMI (r = 0.92), although they are consistently 10±16 % larger in polluted regions (columns >8×10¹⁵ molecules cm⁻²). These differences result primarily from differences in air mass factors.