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HCFC‐22 is an ozone‐depleting substance with a greenhouse effect. The atmospheric mole fractions of HCFC‐22 have been increasing since the 1950s. Within the NDACC‐IRWG network, HCFC‐22 mol fractions can be retrieved from solar absorption spectra measured by ground‐based FTIR. However, only a few sites have provided HCFC‐22 data sets. Here, we demonstrate a harmonized FTIR HCFC‐22 retrieval strategy and generate a new global NDACC‐IRWG HCFC‐22 data set at 16 FTIR sites. The systematic and random uncertainties are 5.3%–8.7% and 3.2%–8.0%, respectively. A maximum HCFC‐22 column annual growth rate was observed in 2009 with a mean of 7.65 ± 1.39 ppt/year, and the HCFC‐22 annual growth rate decreased to 3.57 ± 1.39 ppt/year (2016–2020) and 2.15 ± 2.09 ppt/year (2021–2023). The annual growth rates derived from the FTIR measurements are compared to the ones derived from NOAA surface flask samplings and ACE‐FTS satellite measurements, and the three independent data sets show a good agreement. Plain Language Summary: Monitoring the atmospheric HCFC‐22 mol fraction and its long‐term trend is important to the stratospheric ozone layer and climate change. Ground‐based FTIR measurements within the NDACC‐IWRG community provide a powerful technique for observing atmospheric trace gases. However, due to different retrieval software and procedures among the sites, the record was too heterogeneous for monitoring the global evolution of HCFC‐22 over time. In this study, we propose a harmonized FTIR HCFC‐22 retrieval strategy and generate a global NDACC‐IRWG HCFC‐22 data set at 16 FTIR sites. The retrieval uncertainty of the FTIR HCFC‐22 is well presented and discussed. Based on the new FTIR HCFC‐22 measurements, the HCFC‐22 annual growth rates between 1990 and 2023 are evaluated. The results are compared with two independent data sets: NOAA flask samplings and ACE‐FTS satellite measurements. Good agreement among the three data sets is found, with a clear decrease in the growth rate of atmospheric HCFC‐22 in recent years. According to the latest Montreal Protocol, HCFC‐22 should be phased out within the next 5–6 years. The global FTIR observations will assure continuity into the next years and decades when HCFC‐22 mol fractions should start decreasing after the official phase‐out. Key Points: Implemented a harmonized NDACC‐IRWG FTIR HCFC‐22 retrieval strategy and provided a new global long‐term HCFC‐22 data setA decrease in the growth rate of the atmospheric HCFC‐22 column has been observed by FTIR measurements since 2009The FTIR, NOAA flask samplings, and ACE‐FTS satellite observations show a good agreement in the HCFC‐22 trend [ABSTRACT FROM AUTHOR]

Correct determination of the phase spectrum is a highly relevant task in Fourier Transform Spectrometry for concluding which spectral distribution connects with the measured interferogram. We present implementation of an improved scheme for phase determination in the operational Collaborative Carbon Column Observing Network (COCCON) processor. We introduce a robust unwrapping scheme for retrieving a connected phase spectrum at intermediate spectral resolution, which uses all spectral positions carrying enough signal to allow a significant determination of the phase. In the second step, we perform a least squares fit of model parameters of a suited analytical phase spectrum model through all reliable phase values constructed in the first step. The model fit exploits the fact that we expect the phase to be spectrally smooth. Still, it can be refined to reflect specific characteristics inherent to the optical and electronic layout of the interferometer. The proposed approach avoids the problems of the classical phase reconstruction method, which enforce a spectrally smooth phase by directly limiting spectral resolution when calculating the complex phase. Thereby, the phase is created from a very low number of interferogram points around the centerburst of the interferogram, which results in a suboptimal noise propagation from the interferogram into the spectral domain. Moreover, the interpolation of the phase spectrum across spectral subsections with reduced spectral signal is not well behaved and results depend strongly on the numerical apodization function used for creating the low-resolution phase. [ABSTRACT FROM AUTHOR]

The Total Carbon Column Observing Network (TCCON) and the Infrared Working Group of the Network for the Detection of Atmospheric Composition Change (NDACC-IRWG) are two ground-based networks that provide the retrieved concentrations of up to 30 atmospheric trace gases, using solar absorption spectrometry. Both networks provide reference measurements for the validation of satellites and models. TCCON concentrates on long-lived greenhouse gases (GHGs) for carbon cycle studies and validation. The number of sites is limited, and the geographical coverage is uneven, covering mainly Europe and the USA. A better distribution of stations is desired to improve the representativeness of the data for various atmospheric conditions and surface conditions and to cover a large latitudinal distribution. The two successive Fiducial Reference Measurements for Greenhouse Gases European Space Agency projects (FRM4GHG and FRM4GHG2) aim at the assessment of several low-cost portable instruments for precise measurements of GHGs to complement the existing ground-based sites. Several types of low spectral resolution Fourier transform infrared (FTIR) spectrometers manufactured by Bruker, namely an EM27/SUN, a Vertex70, a fiber-coupled IRCube, and a Laser Heterodyne spectro-Radiometer (LHR) developed by UK Rutherford Appleton Laboratory are the participating instruments to achieve the Fiducial Reference Measurements (FRMs) status. Intensive side-by-side measurements were performed using all four instruments next to the Bruker IFS 125HR high spectral resolution FTIR, performing measurements in the NIR (TCCON configuration) and MIR (NDACC configuration) spectral range. The remote sensing measurements were complemented by AirCore launches, which provided in situ vertical profiles of target gases traceable to the World Meteorological Organization (WMO) reference scale. The results of the intercomparisons are shown and discussed. Except for the EM27/SUN, all other instruments, including the reference TCCON spectrometer, needed modifications during the campaign period. The EM27/SUN and the Vertex70 provided stable and precise measurements of the target gases during the campaign with quantified small biases. As part of the FRM4GHG project, one EM27/SUN is now used as a travel standard for the verification of column-integrated GHG measurements. The extension of the Vertex70 to the MIR provides the opportunity to retrieve additional concentrations of N2O, CH4, HCHO, and OCS. These MIR data products are comparable to the retrieval results from the high-resolution IFS 125HR spectrometer as operated by the NDACC. Our studies show the potential for such types of spectrometers to be used as a travel standard for the MIR species. An enclosure system with a compact solar tracker and meteorological station has been developed to house the low spectral resolution portable FTIR systems for performing solar absorption measurements. This helps the spectrometers to be mobile and enables autonomous operation, which will help to complement the TCCON and NDACC networks by extending the observational capabilities at new sites for the observation of GHGs and additional air quality gases. The development of the retrieval software allows comparable processing of the Vertex70 type of spectra as the EM27/SUN ones, therefore bringing them under the umbrella of the COllaborative Carbon Column Observing Network (COCCON). A self-assessment following the CEOS-FRM Maturity Matrix shows that the COCCON is able to provide GHG data products of FRM quality and can be used for either short-term campaigns or long-term measurements to complement the high-resolution FTIR networks. [ABSTRACT FROM AUTHOR]

The Arctic and boreal regions are experiencing a rapid increase in temperature, resulting in a changing cryosphere, increasing human activity, and potentially increasing high-latitude methane emissions. Satellite observations from Sentinel-5P TROPOMI provide an unprecedented coverage of a column-averaged dry-air mole fraction of methane (XCH4) in the Arctic, compared to previous missions or in situ measurements. The purpose of this study is to support and enhance the data used for high-latitude research through presenting a systematic evaluation of TROPOMI methane products derived from two different processing algorithms: the operational product (OPER) and the scientific product (WFMD), including the comparison of recent version changes of the products (OPER, OPER rpro, WFMD v1.2, and WFMD v1.8). One finding is that OPER rpro yields lower XCH4 than WFMD v1.8, the difference increasing towards the highest latitudes. TROPOMI product differences were evaluated with respect to ground-based high-latitude references, including four Fourier Transform Spectrometer in the Total Carbon Column Observing Network (TCCON) and five EM27/SUN instruments in the Collaborative Carbon Column Observing Network (COCCON). The mean TROPOMI–TCCON GGG2020 daily median XCH4 difference was site-dependent and varied for OPER rpro from −0.47 ppb to 22.4 ppb, and for WFMD v1.8 from 1.2 ppb to 19.4 ppb with standard deviations between 13.0 and 20.4 ppb and 12.5–15.0 ppb, respectively. The TROPOMI–COCCON daily median XCH4 difference varied from −26.5 ppb to 5.6 ppb for OPER rpro, with a standard deviation of 14.0–28.7 ppb, and from −5.0 ppb to 17.2 ppb for WFMD v1.8, with a standard deviation of 11.5–13.0 ppb. Although the accuracy and precision of both TROPOMI products are, on average, good compared to the TCCON and COCCON, a persistent seasonal bias in TROPOMI XCH4 (high values in spring; low values in autumn) is found for OPER rpro and is reflected in the higher standard deviation values. A systematic decrease of about 7 ppb was found between TCCON GGG2014 and GGG2020 product update highlighting the importance of also ensuring the reliability of ground-based retrievals. Comparisons to atmospheric profile measurements with AirCore carried out in Sodankylä, Northern Finland, resulted in XCH4 differences comparable to or smaller than those from ground-based remote sensing. [ABSTRACT FROM AUTHOR]

We describe a method for removing systematic biases of column-averaged dry air mole fractions of CO2 (XCO2) and CH4 (XCH4) derived from short-wavelength infrared (SWIR) spectra of the Greenhouse gases Observing SATellite (GOSAT). We conduct correlation analyses between the GOSAT biases and simultaneously retrieved auxiliary parameters. We use these correlations to bias correct the GOSAT data, removing these spurious correlations. Data from the Total Carbon Column Observing Network (TCCON) were used as reference values for this regression analysis. To evaluate the effectiveness of this correction method, the tnzuncorrected/corrected GOSAT data were compared to independent XCO2 and XCH4 data derived from aircraft measurements taken for the Comprehensive Observation Network for TRace gases by AIrLiner (CONTRAIL) project, the National Oceanic and Atmospheric Administration (NOAA), the US Department of Energy (DOE), the National Institute for Environmental Studies (NIES), the Japan Meteorological Agency (JMA), the HIAPER Pole-to-Pole observations (HIPPO) program, and the GOSAT validation aircraft observation campaign over Japan. These comparisons demonstrate that the empirically derived bias correction improves the agreement between GOSAT XCO2/XCH4 and the aircraft data. Finally, we present spatial distributions and temporal variations of the derived GOSAT biases.

This study describes the digitization and calibration of historically significant solar absorption spectra recorded at the Jungfraujoch International Scientific Station in the 1950s. Using a homemade Pfund-type grating spectrometer, these spectra were recorded on paper rolls to study the solar spectrum which was then used to compile a solar atlas between 2.8 and 23.7 microns (~421 to 3571 cm −1) that later contributed to the development of the HITRAN database. We now digitized these old spectra to make them available for atmospheric studies. Our approach involves image processing techniques, including colour masking for digitization and peak detection for accurate wavenumber calibration against a synthetic spectrum. We also developed a validation method by re-digitizing degraded FTIR spectra to the same resolution as the old spectra to evaluate the digitization accuracy. Furthermore, we studied the influence of line thickness on the digitization error. The number of spectra transformed into a machine-readable format is 108 (freely available for download), with an average digitization error of 1.55 % and a wavenumber shift standard diviation of 0.075 cm −1. These digitized and calibrated spectra now offer a valuable resource for atmospheric studies, providing essential historical data for atmospheric research. This work not only helps to preserve scientific heritage but also enhances the utility of historical data in contemporary research. [ABSTRACT FROM AUTHOR]

This study presented an analysis of the geometric and optical properties of cirrus clouds with data produced by Compact Cloud-Aerosol Lidar (ComCAL) over Koror, Palau (7.3°N, 134.5°E), in the Tropical Western Pacific region. The lidar measurement dataset covers April 2018 to May 2019 and includes data collected during March, July and August 2022. The results show that cirrus clouds occur approximately 47.9% of the lidar sampling time, predominantly between altitudes of 15 and 18 km. Seasonal variations in cirrus top height closely align with those of the cold point tropopause. Most cirrus clouds exhibit low cloud optical depth (COD < 0.1), with an annual mean depolarization ratio of 31 ± 19%. Convective-forming cirrus clouds during the summer monsoon season exhibit a larger size by notably lower values in terms of color ratio. Extremely thin cirrus clouds (COD < 0.005) constituting 1.6% of total cirrus occurrences are frequently observed at 1–2 km above the cold point, particularly during winter and summer, suggesting significant stratosphere–troposphere exchange. The coldest and highest tropopause over Palau is persistent during winter, and related to the pathway of tropospheric air entering the stratosphere through the cold trap. In summer, the extremely thin cirrus above the cold point is likely correlated with equatorial Kelvin waves induced by western Pacific monsoon convection. [ABSTRACT FROM AUTHOR]

Satellite gravimetry is used to study the global hydrological cycle. It is a key component in the investigation of groundwater depletion on the Indian subcontinent. Terrestrial mass loss caused by river sediment transport is assumed to be below the detection limit in current gravimetric satellites of the Gravity Recovery and Climate Experiment Follow-On mission. Thus, it is not considered in the calculation of terrestrial water storage (TWS) from such satellite data. However, the Ganges and Brahmaputra rivers, which drain the Indian subcontinent, constitute one of the world's most sediment-rich river systems. In this study, we estimate the impact of sediment mass loss within their catchments on local trends in gravity and consequential estimates of TWS trends. We find that for the Ganges–Brahmaputra–Meghna catchment sediment transport accounts for (4 ± 2) % of the gravity decrease currently attributed to groundwater depletion. The sediment is mainly eroded from the Himalayas, where correction for sediment mass loss reduces the decrease in TWS by 0.22 cm of equivalent water height per year (14 %). However, sediment mass loss in the Brahmaputra catchment is more than twice that in the Ganges catchment, and sediment is mainly eroded from mountain regions. Thus, the impact on gravimetric TWS trends within the Indo–Gangetic Plain – the main region identified for groundwater depletion – is found to be comparatively small (< 2 %). [ABSTRACT FROM AUTHOR]

We simulated the seasonal temperature evolution in the atmosphere of Antarctica and the Arctic focusing on infrared processes. Contributions by other processes were parametrized and kept fixed throughout the simulations. The model was run for current CO2 and CH4 and for doubled concentrations. For doubling CH4 the warming in Antarctica is restricted to the lowest few hundred meters above the surface while in the Arctic we find a warming in the whole troposphere. We find that the amount of water is the main driver for the differences between both polar regions. When increasing both, CO2 and CH4 from pre‐industrial values to current concentrations, and averaged over the whole troposphere, we find a warming of 0.42 K for the Arctic and a slight cooling of 0.01 K for Antarctica. Our results contribute to the understanding of the lack of warming seen in Antarctica throughout the last decades. Plain Language Summary: In 2015 we have initiated a discussion on a fundamental property of the radiation in the atmosphere over Antarctica: The negative greenhouse effect (Schmithüsen et al., 2015, https://doi.org/10.1002/2015GL066749). A negative greenhouse effect means, the atmosphere emits more radiation to space than it receives from the surface. This results in a cooling somewhere in the Antarctic atmosphere during some months of the year, when increasing CO2. We now simulate how the Antarctic atmospheric temperature responds in all altitude levels to CO2 and CH4 increases, and show this is different from the temperature response in the Arctic. We show for example, that an increase in CH4 cools nearly the whole troposphere, although the response for CH4 is much lower in amplitude than for CO2. We find that the amount of water is the main driver for the differences between both polar regions. Since the amount of water vapor strongly depends on temperature, the colder Antarctic atmosphere responds differently to the Arctic when greenhouse gases increase. Our studies could be one important factor when understanding the lack of warming in Antarctica throughout the last decades. Key Points: We simulate the temperature development in both polar regions in the infrared and find that doubling CO2 and CH4 lead to opposing forcingsThe different amount of water vapor shows to be responsible for the differences in warming/cooling in both polar regionsIn Antarctica doubling CH4 leads to a cooling of almost the whole troposphere, a future increase in H2O could invert this [ABSTRACT FROM AUTHOR]

The Tropospheric Monitoring Instrument (TROPOMI) on board the Sentinel-5 Precursor (S5P) satellite is part of the latest generation of trace gas monitoring satellites and provides a new level of spatio-temporal information with daily global coverage, which enables the calculation of daily globally averaged CH4 concentrations. To investigate changes in atmospheric methane, the background CH4 level (i.e. the CH4 concentration without seasonal and short-term variations) has to be determined. CH4 growth rates vary in a complex manner and high-latitude zonal averages may have gaps in the time series, and thus simple fitting methods do not produce reliable results. In this paper we present an approach based on fitting an ensemble of dynamic linear models (DLMs) to TROPOMI data, from which the best model is chosen with the help of cross-validation to prevent overfitting. This method is computationally fast and is not dependent on additional inputs, allowing for fast and continuous analysis of the most recent time series data. We present results of global annual methane increases (AMIs) for the first 4.5 years of S5P/TROPOMI data, which show good agreement with AMIs from other sources. Additionally, we investigated what information can be derived from zonal bands. Due to the fast meridional mixing within hemispheres, we use zonal growth rates instead of AMIs, since they provide a higher temporal resolution. Clear differences can be observed between Northern Hemisphere and Southern Hemisphere growth rates, especially during 2019 and 2022. The growth rates show similar patterns within the hemispheres and show no short-term variations during the years, indicating that air masses within a hemisphere are well-mixed during a year. Additionally, the growth rates derived from S5P/TROPOMI data are largely consistent with growth rates derived from Copernicus Atmospheric Monitoring Service (CAMS) global-inversion-optimized (CAMS/INV) data, which use surface observations. In 2019 a reduction in growth rates can be observed for the Southern Hemisphere, while growth rates in the Northern Hemisphere stay stable or increase. During 2020 a strong increase in Southern Hemisphere growth rates can be observed, which is in accordance with recently reported increases in Southern Hemisphere wetland emissions. In 2022 the reduction in the global AMI can be attributed to decreased growth rates in the Northern Hemisphere, while growth rates in the Southern Hemisphere remain high. Investigations of fluxes from CAMS/INV data support these observations and suggest that the Northern Hemisphere decrease is mainly due to the decrease in anthropogenic fluxes, while in the Southern Hemisphere, wetland fluxes continued to rise. While the continued increase in Southern Hemisphere wetland fluxes agrees with existing studies about the causes of observed methane trends, the difference between Northern Hemisphere and Southern Hemisphere methane increases in 2022 has not been discussed before and calls for further research. [ABSTRACT FROM AUTHOR]

Soil CO fluxes represent a net balance between biological soil CO uptake and abiotic soil and (senescent) plant CO production. Studies largely from temperate and boreal forests indicate that soils serve as a net sink for CO, but to date uncertainty remains about the role of tropical rain forest soils. Here we report the first direct measurements of soil CO fluxes in a tropical rain forest. We compare with estimates of net ecosystem CO fluxes derived from accumulation of CO at night under stable atmospheric conditions. Further, we used laboratory experiments to demonstrate the importance of temperature on net soil CO fluxes. Net soil surface CO fluxes ranged from -0.19 to 3.36 nmol m-2 s-1, averaging ∼1 nmol CO m-2 s-1. Fluxes varied with season and topographic location, with highest fluxes measured in the dry season in a seasonally inundated valley. Ecosystem CO fluxes estimated from nocturnal canopy air profiles, which showed CO mixing ratios that consistently decreased with height, ranged between 0.3 and 2.0 nmol CO m-2 s-1. A canopy layer budget method, using the nocturnal increase in CO, estimated similar flux magnitudes (1.1 to 2.3 nmol CO m-2 s-1). In the wet season, a greater valley ecosystem CO production was observed in comparison to measured soil valley CO fluxes, suggesting a contribution of the valley stream to overall CO emissions. Laboratory incubations demonstrated a clear increase in CO production with temperature that was also observed in field fluxes, though high correlations between soil temperature and moisture limit our ability to interpret the field relationship. At a common temperature (25 °C), expected plateau and valley senescent leaf CO production was small (0.012 and 0.002 nmol CO m-2 s-1) in comparison to expected soil material CO emission (∼0.9 nmol CO m-2 s-1). Based on our field and laboratory observations, we expect that tropical rain forest ecosystems are a net source of CO, with thermal degradation-induced soil emissions likely being the main contributor to ecosystem CO emissions. Extrapolating our first observation-based tropical rain forest soil emission estimate of ∼1 nmol m-2 s-1, a global tropical rain forest soil emission of ∼16.0 Tg CO yr-1 is estimated. Nevertheless, total ecosystem CO emissions might be higher, since valley streams and inundated areas might represent local CO emission hot spots. To further improve tropical forest ecosystem CO emission estimates, more in-situ tropical forest soil and ecosystem CO flux measurements are essential. [ABSTRACT FROM AUTHOR]

Soil CO fluxes represent a net balance between biological soil CO uptake and abiotic soil and (senescent) plant CO production. Studies largely from temperate and boreal forests indicate that soils serve as a net sink for CO, but to date uncertainty remains about the role of tropical rain forest soils. Here we report the first direct measurements of soil CO fluxes in a tropical rain forest. We compare with estimates of net ecosystem CO fluxes derived from accumulation of CO at night under stable atmospheric conditions. Further, we used laboratory experiments to demonstrate the importance of temperature on net soil CO fluxes. Net soil surface CO fluxes ranged from -0.19 to 3.36 nmol m-2 s-1, averaging ∼1 nmol CO m-2 s-1. Fluxes varied with season and topographic location, with highest fluxes measured in the dry season in a seasonally inundated valley. Ecosystem CO fluxes estimated from nocturnal canopy air profiles, which showed CO mixing ratios that consistently decreased with height, ranged between 0.3 and 2.0 nmol CO m-2 s-1. A canopy layer budget method, using the nocturnal increase in CO, estimated similar flux magnitudes (1.1 to 2.3 nmol CO m-2 s-1). In the wet season, a greater valley ecosystem CO production was observed in comparison to measured soil valley CO fluxes, suggesting a contribution of the valley stream to overall CO emissions. Laboratory incubations demonstrated a clear increase in CO production with temperature that was also observed in field fluxes, though high correlations between soil temperature and moisture limit our ability to interpret the field relationship. At a common temperature (25 ◦C), expected plateau and valley senescent leaf CO production was small (0.012 and 0.002 nmol CO m-2 s-1) in comparison to expected soil material CO emission (∼0.9 nmol CO m-2 s-1). Based on our field and laboratory observations, we expect that tropical rain forest ecosystems are a net source of CO, with thermal degradation-induced soil emissions likely being the main contributor to ecosystem CO emissions. Extrapolating our first observation-based tropical rain forest soil emission estimate of ∼1 nmol m-2 s-1, a global tropical rain forest soil emission of ∼16.0 Tg CO yr-1 is estimated. Nevertheless, total ecosystem CO emissions might be higher, since valley streams and inundated areas might represent local CO emission hot spots. To further improve tropical forest ecosystem CO emission estimates, more in-situ tropical forest soil and ecosystem CO flux measurements are essential. [ABSTRACT FROM AUTHOR]

Nitrous oxide (N2O) and methane (CH4) are two important greenhouse gases in the atmosphere. In 2019, mid-infrared (MIR) solar absorption spectra were recorded by a Bruker VERTEX 70 spectrometer and a Bruker IFS 125HR spectrometer at Sodankylä, Finland, at spectral resolutions of 0.2 and 0.005 cm-1 , respectively. The N2O and the CH4 retrievals from high-resolution MIR spectra have been well investigated within the Network for the Detection of Atmospheric Composition Change (NDACC) but not for MIR spectra gathered with instruments operating at low spectral resolution. In this study, N2O and CH4 retrieval strategies and retrieval uncertainties from the VERTEX 70 MIR low-resolution spectra are discussed and presented. The accuracy and precision of the VERTEX 70 N2O and CH4 retrievals are assessed by comparing them with the coincident 125HR retrievals and AirCore measurements. The relative differences between the N2O total columns retrieved from 125HR and VERTEX 70 spectra are - 0.3 ± 0.7 (1 σ) % with a correlation coefficient (R) of 0.93. Regarding the CH4 total column, we first used the same retrieval microwindows for 125HR and VERTEX 70 spectra, but there is an underestimation in the VERTEX 70 retrievals, especially in summer. The relative differences between the CH4 total columns retrieved from the 125HR and VERTEX 70 spectra are -1.3±1.1 (1 σ) % with a R value of 0.77. To improve the VERTEX 70 CH4 retrievals, we propose alternative retrieval microwindows. The relative differences between the CH4 total columns retrieved from the 125HR and VERTEX 70 spectra in these new windows become 0.0±0.8 (1 σ) %, along with an increase in the R value to 0.87. The coincident AirCore measurements confirm that the VERTEX 70 CH4 retrievals using the latter window choice are better, with relative mean differences between the VERTEX 70 CH4 retrievals and AirCore measurements of - 1.9 % for the standard NDACC microwindows and of 0.13 % for the alternative microwindows. This study provides insight into the N2O and CH4 retrievals from the low-resolution (0.2 cm-1) MIR spectra observed with a VERTEX 70 spectrometer, and it demonstrates the suitability of this kind of instrument for contributing to satellite validation, model verification, and other scientific campaigns with the advantage of its transportability and lower cost compared to standard NDACC-type Fourier-transform infrared (FTIR) instruments. [ABSTRACT FROM AUTHOR]