The Ce 4f part of the electron addition spectra of cerium compounds is
selectively and resonantly enhanced when the excitation energy coinci
des with the Ce 3d-->4f (M(4.5)) absorption edge. Different spectral f
eatures, corresponding to 4f(1) and 4f(2) configurations in the final
state, exhibit distinct resonance profiles. The relative intensities o
f the f(1) and f(2) resonances may vary by as much as a factor of 50,
according to the strength of the hybridization between 4f and conducti
on-band states. At resonance the spectral line shape is unambiguously
modified when the temperature is varied across the characteristic Kond
o temperature.