The effects of TyrD•, TyrZ•, and QA•−radical formation on the absorption spectrum in the Soret region were studied in Mn-depleted Photosystem II at pH 8.6 (in order to be in the TyrDstate after the dark adaptation). Flash-induced difference spectra were recorded in several PSII samples from i) Thermosynechococcus vestitus (formerly T. elongatus), ii) Synechocystis sp. PCC 6803, iii) Chroococcidiopsis thermalis PCC7203 grown under far-red light, and iv) Acaryochloris marina. In the case of T. vestitus, mutants D1/H198Q, D1/T1789H, D2/I178H and D2/Y160F, with PsbA1/Q130 instead of PsbA3/E130, were also studied for possible contributions from PD1, ChlD1, ChlD2 and PheD1, respectively. For a possible contribution from PD2, the D2/H197A mutant was studied in S. 6803. While PD1 is clearly the species whose spectrum is blue shifted by ~ 3 nm in the presence of QA•−, as already well documented in the literature, the species whose spectra are shifted upon the formation of TyrD•, and TyrZ•remain to be clearly identified as they appear different from PD1, PD2, PheD1, ChlD1 and ChlD2 as concluded by the lack of different light-induced difference spectra in the mutants listed above. Although we cannot rule out too weak effect taking into account the accuracy of the experiments, it is proposed that other pigments are involved as antenna Chl and/or Car near the reaction center. Additionally, it is shown that, i) there is no proton release into the bulk upon the oxidation of TyrDat pH 8.6, and ii) the rearrangement of the electrostatic environment of the pigments involved in the light-induced different spectra in the samples studied upon the formation TyrD•, TyrZ•, and QA•−likely occur differently on a kinetic and structural point of views.