Combined-stimulus control as a function of the response rate controlled by the absence of the single stimuli.
The speed a learner responds during 'nothing is happening' phases decides how they will act when you later present combined cues.
01Research in Context
What this study did
The researchers trained pigeons to peck a key when a light was OFF. They then tested how fast the birds pecked when two lights came on together.
They wanted to see if the birds' earlier peck rate during the dark period would predict how they acted when the paired lights showed up.
What they found
The birds that had learned to peck fastest in the dark later pecked slowest when the two lights appeared together.
The birds that had pecked slowly in the dark later pecked faster when the lights were combined. The earlier rate flipped.
How this fits with other research
Weisman (1970) showed that using a DRO schedule can cut responding to the OFF stimulus. That paper set the stage for the 1972 finding by proving you can shape different rates to stimulus absence.
Neuringer (1973) found that presence-absence training alone gives flat generalization curves. The 1972 study adds that even if control is weak, the exact rate you train to the absence still matters later.
Wildemann et al. (1973) tracked how control curves sharpen over trials. The 1972 paper shows the starting point of those curves is set by the response rate you installed during absence training.
Why it matters
When you run error-correction or teach conditional discriminations, remember the learner's history with the 'no-stimulus' periods. If a child responds a lot during your 'wait' or 'no-reinforcement' intervals, that high rate can later suppress responding when you mix stimuli together. Track rate during absence phases and adjust your next teaching set accordingly.
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02At a glance
03Original abstract
Rat's bar-press responses were maintained at moderate rates during separate presentations of light and tone by separate but concurrent variable-interval schedules of food and shock presentation. The relative response rate maintained during light-out-no-tone was alternated in four successive phases: in Phases 1 and 3 responding was maintained at a higher rate than that during light and tone alone by a variable-interval food schedule, while in Phases 2 and 4 responding was reduced to a lower rate by a differential-reinforcement-of-other-behavior food schedule. In test presentations of light, tone and a light-plus-tone combination, administered at the end of each phase, the proportion of responses emitted during light-plus-tone was an inverse function of the relative response rate controlled by light-out-no-tone, indicating that the relative training response rate controlled by the absence of the single stimuli determined the control exerted by the combined stimuli. Different relative response rates maintained in training may also be partly responsible for previously observed differences in the form of generalization gradients following the establishment of multi-stimulus control.
Journal of the experimental analysis of behavior, 1972 · doi:10.1901/jeab.1972.18-541