Light-induced redox processes have been established as cause of the chromatic alterations of a number of artists’ pigments used from 15th to 20th century. Despite, the fact that a general comprehension of the mechanisms has been provided through the characterization of the photo-degraded compounds, both exhaustive information on the wavelength-dependence of the alteration process of the pigments and experimental evidences in how the visible light may influence the formation pathways of specific secondary compounds are still lacking. Establishing an analytical protocol for the study of wavelength-dependence of pigments photo-redox pathways is relevant for a safe illumination of paintings, especially in view of the possible use of spectrally tunable light source such as white light emitting diodes (WLEDs). In this work, we propose an integrated approach based on a combination of diffuse reflectance UV-Visible, SR-based micro X-ray fluorescence (µ-XRF)/X-ray absorption near edge structure (µ-XANES) and electron paramagnetic resonance (EPR) spectroscopies for study the photo-redox process Cr(VI)→Cr(III) for lead chromate yellows (PbCr1-xSxO4, 0≤x≤0.8) under exposure to different monochromatic lights. In view of the thin (3-5 μm) alteration layer that is formed at the paint surface after light exposure, SR-based Cr K-edge μ-XANES/μ-XRF analysis were employed to obtain information on the abundance, nature and distribution of the alteration of Cr(III)-compounds at the micrometric-scale level. On the other hand, EPR spectroscopy was used as complementary tool to the SR-based X-ray methods due to its sensitivity for revealing species containing one or more unpaired electrons and for distinguishing different coordination geometry of paramagnetic centers, such as Cr(V)-species. Semi-quantitative indications about the darkening of the paint surface were obtained by UV-Vis spectroscopy. An abundance of reduced Cr down to around 50% was detected at the aged surface of the chrome yellow paints. The reduction process was favored not only by wavelengths shorter than 460 nm (i.e., where the pigment shows its maximum absorption) but also by light in the 490-530 nm range. A first evidence of the presence of Cr(V)-intermediates in the Cr(VI)→Cr(III) reduction reaction allowed the risks of inducing photo-degradation of the 490-530 nm wavelength range to be explained.