“…However, an alternative means of controlling prior trial history was suggested to us by a reviewer, which we also opted to carry out. This procedure derives from the work of Jones and Sieck (2003) and, in the context of the present work, involves looking at priming effects in the following way: We computed mean RTs as a function of whether the target on trial n was a repetition or alternation from trial n − 1 and as a function of whether the target on trial n − 1 was a repetition or alternation from trial n − 2. This yields four trial types (repeat-repeat, repeat-switch, switch-repeat, switchswitch), allowing us to average repeat-repeat and switchrepeat trials together to get a measure of a target repetition from trial n − 1 to trial n, with prior history controlled for, and to average repeat-switch and switch-switch trials together to get a measure of a target switch from trial n − 1 to trial n, with prior trial history controlled for, while maintaining large cell sizes.…”