Understanding the distribution of atmospheric water vapor (H₂O) is crucial for global warming studies and climate change mitigation. In this study, we retrieved the ground layer, tropospheric and total columns of H₂O using ground-based high-resolution Fourier transform infrared spectrometry (FTIR). The H₂O total columns are obtained from near-infrared (NIR) and mid-infrared (MIR) spectra, and the ground layer and tropospheric H₂O columns are retrieved from the MIR spectrum. The total columns of H₂O retrieved from NIR and MIR have a good consistency (R = 0.989). Additionally, the ground layer H₂O columns have a similar seasonal variation to total columns and tropospheric columns but have a higher seasonal amplitude. The ground layer H₂O columns are close to the total columns and tropospheric columns in winter; however, in summer, the average difference between the ground layer and total columns and the value between the ground layer and tropospheric columns are large. This is mostly due to temperature variation. The temperature has a linear response to H₂O, and the relationship between surface temperature and ln(XH₂O) values in the ground layer, the entire atmosphere and the troposphere show a significantly positive correlation, and the correlation coefficient R is 0.893, 0.882 and 0.683, respectively. Furthermore, we selected the HYSPLIT model to simulate the back trajectories of air parcels in the four seasons in Hefei and find that the air mass transport has a significant impact on the local H₂O change. These results demonstrate that ground-based high-resolution FTIR technology has high accuracy and precision in observing the vertical distribution and seasonal changes of H₂O in different atmospheres.

Studies of the impact of biomass burning and the emissions of trace gases from biomass burning, especially using long-term observations, are scarce in China. We utilize solar absorption spectra obtained via ground-based high-resolution Fourier transform infrared (FTIR) spectroscopy to retrieve the atmospheric total columns and vertical profiles of carbon monoxide (CO), formaldehyde (H₂CO), and hydrogen cyanide (HCN) in Hefei, China. Seasonal and interannual variability in the three gases from 2016 to 2022 are analyzed. Atmospheric CO shows significant seasonal variations, peaking during spring and winter, and declining during summer, with a seasonal amplitude of 8.07 × 10¹⁷ molecules cm⁻² and a seasonal variability of 29.35%. H₂CO and HCN have similar seasonal patterns to each other, with high concentrations in summer and low concentrations in winter. The seasonal amplitude of H₂CO and HCN are 1.89 × 10¹⁶ molecules cm⁻² and 2.32 × 10¹⁵ molecules cm⁻², respectively, with a seasonal variability of 133.07% and 34.69%, respectively. The means of the annual variation rate for CO, H₂CO, and HCN are (−2.67 ± 2.88)% yr⁻¹, (2.52 ± 12.48)% yr⁻¹ and (−3.48 ± 7.26)% yr⁻¹, respectively. To assess the influence of biomass burning on the variations in column concentrations of the three gases, the correlation between CO, H₂CO, and HCN was analyzed. The months during which the monthly correlation coefficient between CO and H₂CO with HCN exceeds 0.8, and the fire radiative power (FRP) observed by satellites is larger than its monthly average are regarded as a biomass-burning occurrence in Anhui province. Additionally, the enhancement ratios of ΔH₂CO/ΔCO and ΔHCN/ΔCO were calculated for the periods impacted by the biomass burning. Finally, backward trajectory cluster analysis and the potential source contribution function (PSCF) calculation identified the air mass transport pathways and the potential source areas at the Hefei site.