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Summary form only given. Filamentation of Mid-IR pulses in ambient air is significantly more complicated and challenging as compared to near-IR filaments, due the changing sign of dispersion in the vicinity of 3.6 μm, substantially lower ionization rates and hence plasma density [1], as well as because of the presence of molecular resonances around the atmospheric transparency windows. Experimental observations reveal that despite its low concentration in ambient air, which is only 400-600 ppm (0.04-0.06%), CO2 strongly affects filamentation of 3.9-μm pulses by influencing spectral and temporal dynamics, as well as spatial beam transformations and propagation losses. As a main loss mechanism during filamentation of loosely focused 3.9-μm pulses in ambient air, dynamic absorption by CO2 is identified. Since in the case of loose focusing plasma density in the filament is negligible, pulses during filamentation in both main constituents, O2 and N2, experience pronounced red-sided broadening (Fig.1a), which is governed by stimulated Raman scattering. In ambient air, newly generated spectral components roll over CO2 resonant absorption band situated in the vicinity of 4.2-μm and are effectively absorbed, which results in up to 50% filamentation losses. To our surprise, an increase of CO2 concentration to ~5% level (by exhaling air [3] into 2-m long open-ended tube) leads to complete disappearance of losses.