Likely spatial distributions of network-modifying (and mobile) cations in (oxide) glasses are discussed here. At very low modifier concentrations, the ions form dipoles with non-bridging oxygen centres while, at higher levels of modification, the cations tend to order as a result of Coulombie interactions. Activation energies for cation migration are calculated, assuming that the ions occupy (face-sharing) oetahedrai ~ites. It is found that conductivity activation energy decreases markedly with increasing modifier content, in agreement with experiment.