(X 3 − g , v). In contrast to the previous models of kinetics of O 2 (a 1 g ) and O 2 (b 1 + g ), our model takes into consideration the following basic facts: first, photolysis of O 3 and O 2 and the processes of energy exchange between the metastable products of photolysis involve generation of oxygen molecules on highly excited vibrational levels in all considered electronic states -b 1 + g , a 1 g and X 3 − g ; second, the absorption of solar radiation not only leads to populating the electronic states on vibrational levels with vibrational quantum number v equal to 0 -O 2 (b 1 + g , v=0) (at 762 nm) and O 2 (a 1 g , v=0) (at 1.27 µm), but also leads to populating the excited electronicvibrational states O 2 (b 1 + g , v=1) and O 2 (b 1 + g , v=2) (at 689 nm and 629 nm). The proposed model allows one to calculate not only the vertical profiles of the O 2 (a 1 g , v=0) and O 2 (b 1 + g , v=0) concentrations, but also the profiles of2)] and O 2 (X 3 − g , v=1-35). In the altitude range 60-125 km, consideration of the electronic-vibrational kinetics significantly changes the calculated concentrations of the metastable oxygen molecules and reduces the discrepancy between the altitude profiles of ozone concentrations retrieved from the 762-nm and 1.27-µm emissions measured simultaneously.