The properties of the perovskite-type La1-xSrxMnO3+/-delta oxides (0 less than or equal to x less than or equal to 1) are related to the reversible redox reaction of manganese ions Mn3+ <-> Mn4-. This reaction plays an essential role both in the interfacial transfers and transport properties and depends on relative cation concentrations and experimental conditions. In this paper we present experimental investigations aiming to determine, to compare and to control some of the surface and bulk properties of these oxides. The bulk and surface Mn4+ contents were investigated by thermogravimetry analysis (TGA) in hydrogen and X-ray photoelectron spectroscopy (XPS) respectively. With a finely divided La0.8Sr0.2MnO3 powder, the chemical composition in the surface layers was found to be practically independent of the conditions of a high temperature treatment in oxygen. The same is true for the mean oxidation state of manganese always close to Mn4+. With pellets of various compositions (x = 0, 0.2, 0.5 and 1), enrichment in strontium with respect to the bulk composition was detected in oxygen at high temperature and found to depend on the strontium concentration in the bulk. Moreover, for any chemical composition, deficit in manganese were systematically evidenced in the surface layers. Surface strontium concentration and mean oxidation state of manganese was correlated as expected. By comparing the results observed with very finely divided powder and pellets respectively, it was deduced that the grain boundaries have an important effect on the surface composition. Data on the structural evolution of the initial compounds during their hydrogen reduction are also presented.