In this work, the temperature and high-pressure behaviors of Mn 3+ -doped garnet-type Ca 3 Ga 2 Ge 3 O 12 single crystals have been investigated by means of photoluminescence and Raman spectroscopy, respectively. The Jahn−Teller stabilization energy in the 5 E ground state was found to be 1630 cm −1 , being as much as 6 times greater than that in the 5 T 2 excited state, that is, 237 cm −1 . The room-temperature emission spectrum is dominated by the spin-allowed 5 T 2 → 5 E transition at 670 nm upon 532 nm excitation. The temperature dependences of photoluminescence spectra and time decays reveal strong thermalization between 5 T 2 and 1 T 2 levels. Cooling to 50 K empties the 5 T 2 level by virtue of multiphonon transition to the lower-lying 1 T 2 level. As a result, the 1 T 2 → 3 T 1 / 5 E electric-dipole transitions are induced by coupling to odd-parity phonons. The existence of a small amount of Mn 4+ can be ascertained by lowering the temperature or applying high pressure. Upon compression up to 100 kbar, the 5 T 2 → 5 E transition of Mn 3+ undergoes a blue shift at a rate of ∼10.5 cm −1 /kbar. Since both 5 T 2 and 1 T 2 have inverse crystal field dependences, the quenching process from the 5 T 2 level becomes stronger under high pressure. Cryogenic luminescence ratiometric thermometry based on the diverse thermal quenching behaviors of Mn 3+ and Mn 4+ was explored. Furthermore, theoretical calculations employing the exchange-charge model of crystal field for Mn 3+ and Mn 4+ ions in Ga 3+ octahedral sites (C 3i ) in garnet-type Ca 3 Ga 2 Ge 3 O 12 remain in perfect agreement with the experimental data.