In BaTiO3 the alkali ions Na and K, replacing Ba, lead to acceptor lev
els about 50 meV above the valence band edge. The structure of these d
efects can be studied by electron spin resonance, after light induced
valence-band holes have been captured at neighboring O2- ions. Hyperfi
ne interaction with Na, Ba, and Sr impurities, adjacent to the paramag
netic O-, is-identified. The holes are trapped stably below similar to
50 K. Their level position is determined by the temperature dependenc
e of the relaxation rate of the light-induced nonequilibrium excess ho
le population. Photostimulated small polaron transfer between O2- site
s equivalent with respect to Na or K leads to a strong optical-absorpt
ion band with peak at 1.3 eV, corresponding to a stabilization energy
of the bound hole polaron of about 0.65 eV. The Na+-O- dipoles can be
reoriented under uniaxial stress at 4.2 K; a differential stress coupl
ing coefficient of 1.23x10(-4) m(3) is derived. Several O- centers ass
ociated with partly unassigned accepters on Ti sites are identified. T
heir properties are compared to those of the Ba site accepters. Vibron
ic g shifts are accounted for by a dynamic Jahn-Teller effect involvin
g the twofold degenerate O- pi orbitals.