anable pulsed laser ablation mass spectra were obtained for barium-containing solids, BaTiO,, Ba3Lu-4Ti-xO, and BaF,, for k450-475 nm with target irradiances of -106-108 W cm-'. Ablated positive ions identified by time-of-flight mass spectrometry included Ba2+, F', 0' and Ti', each of which exhibited an intensity maximum near b=455.4 nm (2.72 eV), which corresponds to the Ba' transition from the 6s zS,,, ground state to the 6p 2P312 excited state. The observed resonant Ba" yield enhancement suggests that some excited Ba+* acquired sufficient additional energy from the ablation plasma to further ionize (IE(Ba' +Ba2'}= 10.00 eV). The simultaneous secondary enhancement in +1 ion yields for other elements suggests collisional energy transfer from Ba+* to atomic or molecular plume species, exciting them to more easily ionized states. Although the detailed energy transfer mechanisms are indefinite, the general observations indicate that resonantly pumping energy into Ba' heats the ablation plume With some species-selectivity. No significant wavelength-dependence was evident in the yields of BaX' from the gas-phase reactions of ablated Ba' with C,oF,, (X=F), CCI, (X=Cl), Br, (X=Br), CH31 (X=I) and CH,OH (X=OH and OCH,). These observations reflect that the radiative lifetime of Ba+* 2P,,2 is only 6 ns, dictating that primarily ground state Ba' encounter ambient reactants as the ablation plume expands.