Zolal Ayazpour

and 31 more

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).

Kelley C. Wells

and 10 more

Isoprene is the dominant non-methane organic compound emitted to the atmosphere, where it drives ozone and aerosol production, modulates atmospheric oxidation, and interacts with the global nitrogen cycle. Isoprene emissions are highly variable and uncertain, as is the non-linear chemistry coupling isoprene and its primary sink, the hydroxyl radical (OH). Space-based isoprene measurements can help close the gap on these uncertainties, and when combined with concurrent formaldehyde data provide a new constraint on atmospheric oxidation regimes. Here we present a next-generation machine-learning isoprene retrieval for the Cross-track Infrared Sounder (CrIS) that provides improved sensitivity, lower noise, and thus higher space-time resolution than earlier approaches. The Retrieval of Organics with CrIS Radiances (ROCR) isoprene measurements compare well with previous space-based retrievals as well as with the first-ever ground-based isoprene column measurements, with 20-50% discrepancies that reflect differing sources of systematic uncertainty. An ensemble of sensitivity tests points to the spectral background and isoprene profile specification as the most relevant uncertainty sources in the ROCR framework. We apply the ROCR isoprene algorithm to the full CrIS record from 2012-2020, showing that it can resolve fine-scale spatial gradients at daily resolution over the world’s isoprene hotspots. Results over North America and Amazonia highlight emergent connections between isoprene abundance and daily-to-interannual variations in temperature, nitrogen oxides, and drought stress.

James W Hannigan

and 33 more

Carbonyl sulfide (OCS) is a non-hygroscopic trace species in the free troposphere and the primary sulfur reservoir maintained by direct oceanic, geologic, biogenic and anthropogenic emissions and the oxidation of other sulfur-containing source species. It’s the largest source of sulfur transported to the stratosphere during volcanically quiescent periods. Data from 22 ground-based globally dispersed stations are used to derive trends in total and partial column OCS. Middle infrared spectral data are recorded by solar-viewing Fourier transform interferometers that are operated as part of the Network for the Detection of Atmospheric Composition Change between 1986 and 2020. Vertical information in the retrieved profiles provides analysis of discreet altitudinal regions. Trends are found to have well-defined inflection points. In two linear trend time periods ~2002 - 2008 and ~2008 - 2016, tropospheric trends range from ~0.0 to (1.55 ± 0.30 %/y) in contrast to the prior period where all tropospheric trends are negative. Regression analyses show strongest correlation in the free troposphere with anthropogenic emissions. Stratospheric trends in the period ~2008 - 2016 are positive up to (1.93 ± 0.26 %/y) except notably low latitude stations that have negative stratospheric trends. Since ~2016, all stations show a free tropospheric decrease to 2020. Stratospheric OCS is regressed with simultaneously measured N$_2$O to derive a trend accounting for dynamical variability. Stratospheric lifetimes are derived and range from (54.1 ± 9.7)y in the sub-tropics to (103.4 ± 18.3)y in Antarctica. These unique long-term measurements provide new and critical constraints on the global OCS budget.