The measurement of "switch costs" is held to be of interest because, as is
widely believed, they may reflect the control processes that are engaged wh
en subjects switch between two (or more) competing tasks. [In task-switchin
g experiments, the reaction time (RT) switch cost is typically measured as
the difference in RT between switch and non-switch (repeat) trials.] In thi
s report we focus on the RT switch costs that remain even after the subject
has had some time to prepare for the shift of task, when the switch cost m
ay be approximately asymptotic (so-called residual switch costs). Three exp
eriments are presented. All three experiments used Stroop colour/word, and
neutral stimuli. Participants performed the two tasks of word-reading and c
olour-naming in a regular, double alternation, using the "alternating runs"
paradigm (R. D. Rogers & S. Monsell, 1995). The experiments were designed
to test the hypothesis that RT switch costs depend on a form of proactive i
nterference (PI) arising from the performance of a prior, competing task. A
. Allport, E. A. Styles and S. Hsieh (1994) suggested that these PI effects
resulted from "task-set inertia", that is, the persisting activation-suppr
ession of competing task-sets, or competing task-processing pathways. The r
esults confirmed the existence of long-lasting PI from the competing task a
s a major contributor to switch costs. Non-switch trials, used as the basel
ine in the measurement of switch costs, were also shown to be strongly affe
cted by similar PI effects. However, task-set inertia was not sufficient to
account for these results. The results appeared inconsistent also with all
other previous models of task switching. A new hypothesis to explain these
between-task interference effects was developed, based on the stimulus-tri
ggered retrieval of competing stimulus-response (S-R) associations, acquire
d (or strengthened) in earlier trials. Consistent with this retrieval hypot
hesis, switch costs were shown to depend primarily on the S-R characteristi
cs of the preceding task (the task that was switched from) rather than the
upcoming task. Further, the effects of the other, competing task were found
to persist over many successive switching trials, affecting switch costs l
ong after the stimulus overlap (and hence the principal S-R competition) be
tween the current tasks had been removed. Switch costs were also found to b
e affected by recent, item-specific experience with a given stimulus, in ei
ther the same or the competing task. Finally, the results showed that switc
h costs were massively affected by the ratio of the number of prior trials,
in response to the same stimuli, that had implemented either the currently
intended or the competing S-R mappings. None of these effects are predicte
d by current models of residual switch costs, which appeal to the differenc
es in control processes assumed to be engaged in switch versus non-switch t
rials.