-lauryl-N,N-dimethylamine-N-oxide (LDAO) is used to suspend the RCs, the excited state of the primary electron donor (P*) decays to the ground state with an average lifetime at 77 K of 330 or 170 ps, respectively; however, in both cases the time constant obtained from single-exponential fits varies markedly as a function of the probe wavelength. These findings on the D LL RC are most easily explained in terms of a heterogeneous population of RCs. Similarly, the complex results for D LL -FY L F M in Deriphatglycerol glass at 77 K are most simply explained using a model that involves (minimally) two distinct populations of RCs with very different photochemistry. Within this framework, in 50% of the D LL -FY L F M RCs in Deriphat-glycerol glass at 77 K, P* deactivates to the ground state with a time constant of ∼400 ps, similar to the deactivation of P* in the D LL mutant at 77 K. In the other 50% of D LL -FY L F M RCs, P* has a 35 ps lifetime and decays via electron transfer to the M branch, giving P + H M -in high yield (g80%). This result indicates that P* f P + H M -is roughly a factor of 2 faster at 77 K than at 295 K. In alternative homogeneous models the rate of this M-side electron-transfer process is the same or up to 2-fold slower at low temperature. A 2-fold increase in rate with a reduction in temperature is the same behavior found for the overall L-side process P* f P + H L -in wild-type RCs. Our results suggest that, as for electron transfer on the L side, the M-side electron-transfer reaction P* f P + H M -is an activationless process.