The damage morphology on AA7050-T7451 plate in chromate-containing environments was studied in a simulated fastener-plate arrangement utilizing x-ray tomography. Constant potential holds near the galvanic couple potential provided additional characterization of the damage morphologies. Exposures were conducted in NaCl with the addition of three different chromate concentrations of 0.1 mM, 1 mM, and 10 mM Na 2 CrO 4 . Both x-ray tomography of fastener-plate arrangements and supplemental potentiostatic polarization of planar electrodes showed that the density of local corrosion sites was significantly reduced with the addition of soluble chromate. However, aggressive conditions such as galvanic coupling led to surviving local corrosion sites that were 30 to 40 times deeper in concentrated chromate environments relative to chromate-free environments. To understand these findings, the effect of chromate on the anodic kinetics of AA7050-T7451 and Al-Zn-Mg-Zr (Cu-free 7000), and on the cathodic oxygen reduction reaction (ORR) kinetics of Type 316 stainless steel, pure Cu, Cu replated on AA7050-T74751, and Al 2 CuMg (S phase) were subsequently investigated. Sodium chromate reduced ORR cathodic kinetics by at least one order of magnitude on Type 316 stainless steel and S phase and by less than one order of magnitude on pure Cu. However, additions of sodium chromate did not inhibit ORR cathodic kinetics on AA7050-T7451 when Cu was replated prior to cathodic tests in chromate-containing solutions. In 0.5 M NaCl environments, pitting potentials were raised on AA7050-T7451 upon the addition of chromate and S-phase dissolution was inhibited. These results support the notion that fastener-plate pit density can be reduced by chromate but that the anodic reaction rates in surviving deep localized corrosion sites are not reduced due to a variety of factors that are discussed. Ramifications toward fatigue initiation are discussed.