The uptake of Crsl-chromate by thymocytes in suspension can be used as a sensitive quantitative criterion for the evaluation of early radiation damage to these cells, often under situations where other methods of assessing cell death such as morphological changes do not yield valid results. 'I'he development of a radiation lesion is characterized by a reduction in the uptake of Cr5l, which in vitro can be detected 1 hour following irradiation and with doses as low as 25 rads. By means of this technique thymocytes have been shown to be completely protected by anoxia to doses of up to 150 rads, but a t higher levels anoxia affords little protection. No protection of thymocytes could be demonstrated in vivo with S,P-aminoethylisothiouronium bromide hydrobromide (AET) or serotonin a t 0.72 mmoles per kg. L-Cysteine, cysteamine, and serotonin a t 1 m M concentration in vitro showed no protection of thymocytes provided they were removed from the cells iminediately subsequent to irradiation.