We investigated thermally activated ionization and thermally activated crossover as the two possibilities of quenching of 5d luminescence in Pr 3+ -doped Y 3 Al 5−x Ga x O 12 . Varying the Ga content x gives the control over the relative energy level location of the 5d and 4f 2 :3 PJ states of Pr 3+ and the host conduction band (CB). Temperature-dependent luminescence lifetime measurements show that the 5d luminescence quenching temperature T 50% increases up to x = 2 and decreases with further increasing Ga content. This peculiar behavior is explained by a unique transition between the two quenching mechanisms which have an opposite dependence of thermal quenching on Ga content. For low Ga content, thermally activated crossover from the 4f 5d state to the 4f 2 ( 3 PJ ) states is the operative quenching mechanism. With increasing Ga content, the activation energy for thermally activated crossover becomes larger, as derived from the configuration coordinate diagram, while from the vacuum referred binding energy diagram the activation energy of thermal ionization becomes smaller. Based on these results, we demonstrated that the thermal quenching of Pr 3+ : 5d 1 -4f luminescence in Y 3 Al 5−x Ga x O 12 with x = 0, 1, 2 is a thermally activated crossover while for x = 3, 4, 5 it results from the thermal ionization.