The surface basic sites at the surface of calcium oxide have been explored following the interaction of nitric oxide with the solid by EPR. Various paramagnetic species are formed depending on the pressure of the gas contacted with the solid. In the initial steps of the interaction, a small amount of a NO32- species is formed probably because of the presence at the surface of "anomalous" peroxy or peroxo-like groups. For higher NO pressures, four types of NO22- surface species characterized by distinct values of the g and hyperfine tensors are formed by addition of the neutral molecule to basic O2- sites of the surface. The process involves a considerable rearrangement of the spin distribution with respect to the NO molecule with a net decrease of the. electron spin density on the N atom. The number of basic sites involved in this interaction is very low and amounts to a value in the range of 0.25-0.5% of the whole surface. These active sites are low coordination sites present at morphological defects of the polycrystalline solid. The concentration of the basic sites is 25 times greater than that of the corresponding sites on MgO thus confirming the higher overall basicity of CaO with respect to magnesium oxide. The surface activity shown by MgO and consisting in a low energy interaction of Lewis acid sites with the NO molecule is, on CaO, totally suppressed.