We reported the optical conductivity spectra of the Ruddlesden-Popper series ruthenates, i.e., Sr n+1 Ru n O 3n+1 and Ca n+1 Ru n O 3n+1 , where n =1, 2, and ϱ. Among various optical transitions, we investigated two Ru-O related modes, i.e., the charge-transfer excitation and the transverse stretching phonon. We found that their frequency shifts are not much affected by a structural dimensionality, but are closely related to the Ru-O bond length. Through the quantitative analysis of the charge-transfer excitation energy, we could demonstrate that the p -d hybridization should play an important role in determining their electronic structure. In addition, we discussed how the electronic excitation could contribute the lattice dynamics in the metallic ruthenates.