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The Cross-track Infrared Sounder (CrIS) aboard the Suomi National Polar-orbiting Partnership (S-NPP) satellite is a spaceborne Fourier transform infrared spectrometer. The study aims to retrieve carbon dioxide (CO2) information (the CO2 profile and column-averaged dry-air mole fraction of XCO2) from June 2018 to December 2019 based on the The National Oceanic and Atmospheric Administration (NOAA)-Unique Combined Atmospheric Processing System (NUCAPS) Cloud-Cleared Radiances (CCRs) via the CrIS. The CCRs products for the CrIS with 2223 channels have been available since 22 May 2018. Characteristics of the CO2 weighting functions inform the choice of multiple channels that are around 15 μm in size that differ by latitude and season to maximize retrieval sensitivity to CO2 and minimize sensitivity to other interfering atmospheric parameters. CO2 was retrieved from these channels using an adopted nonlinear optimization algorithm. The temperature, water vapor, and ozone profiles used in the inversion process were gathered from the European Centre for Medium-Range Weather Forecasts (ECMWF) Reanalysis v5 (ERA5). Validations of CO2 concentrations as retrieved from CrIS showed the following conclusions: (1) The relative error of the retrieved CO2 concentrations, as compared to Civil Aircraft for the Regular Investigation of the atmosphere Based on an Instrument Container (CARIBIC) in situ aircraft measurements, was less than 0.5%, and the root mean square errors (RMSE) were less than 0.7 ppmv (with correlation coefficients of 0.56–0.86); (2) the retrieved XCO2 from June 2018 to December 2019 correlated well with the ground-based Total Carbon Column Observing Network (TCCON) observations, and the differences were within ±0.2 ppmv. Further analysis of the temporal and spatial distribution of the retrieved CO2 at 300 hPa demonstrated a strong seasonal variation of CO2 in 0–60° N in the Northern Hemisphere with the maximum values in June–August and larger amplitudes of seasonal variation in the northeast of Asia and northeastern part of North America. The variations likely occurred due to larger sinks of atmospheric CO2 that are dominated by CO2 uptake in the summer. In the Southern Hemisphere, the CO2 displayed high concentration anomalies in the latitudinal range of 30–60° S in September–November and December–February, which probably occurred due to the lofted smoke plumes from the strong fire seasons in South America and Southern Africa. [ABSTRACT FROM AUTHOR]

It has been found that the concentration of atmospheric methane (CH4) has rapidly increased since 2007 after a decade of nearly constant concentration in the atmosphere. As an important greenhouse gas, such an increase could enhance the threat of global warming. To better quantify this increasing trend, a novel statistic method, i.e. the Ensemble Empirical Mode Decomposition (EEMD) method, was used to analyze the CH4 trends from three different measurements: the mid–upper tropospheric CH4 (MUT) from the space-borne measurements by the Atmospheric Infrared Sounder (AIRS), the CH4 in the marine boundary layer (MBL) from NOAA ground-based in-situ measurements, and the column-averaged CH4 in the atmosphere (XCH4) from the ground-based up-looking Fourier Transform Spectrometers at Total Carbon Column Observing Network (TCCON) and the Network for the Detection of Atmospheric Composition Change (NDACC). Comparison of the CH4 trends in the mid–upper troposphere, lower troposphere, and the column average from these three data sets shows that, overall, these trends agree well in capturing the abrupt CH4 increase in 2007 (the first peak) and an even faster increase after 2013 (the second peak) over the globe. The increased rates of CH4 in the MUT, as observed by AIRS, are overall smaller than CH4 in MBL and the column-average CH4. During 2009–2011, there was a dip in the increase rate for CH4 in MBL, and the MUT-CH4 increase rate was almost negligible in the mid-high latitude regions. The increase of the column-average CH4 also reached the minimum during 2009–2011 accordingly, suggesting that the trends of CH4 are not only impacted by the surface emission, however that they also may be impacted by other processes like transport and chemical reaction loss associated with [OH]. One advantage of the EEMD analysis is to derive the monthly rate and the results show that the frequency of the variability of CH4 increase rates in the mid–high northern latitude regions is larger than those in the tropics and southern hemisphere. [ABSTRACT FROM AUTHOR]