“…It is well-known that information on the nature of R 3+ environments, in terms of symmetry and covalence of bonds to the ligands, can be derived from the crystal field analysis of the optical spectra of R 3+ centers in their hosts. From this point of view, changes around R 3+ involving variations in symmetry, interatomic distances, and covalence with neighboring ligands, as for those that result from the partial or total substitution for other R 3+ , − or by tuning temperature and pressure, are usually tested from the crystal field analysis of spectroscopic data derived from optical absorption, photoluminescence (including the fluorescence line narrowing technique, for glass materials), and inelastic neutron scattering experiments.…”