ABA Fundamentals

Interactions in multiple schedules: negative induction with squirrel monkeys.

Spealman (1978) · Journal of the experimental analysis of behavior 1978
★ The Verdict

Negative induction in multiple schedules is brief and species-specific, so watch for fleeting response dips when you alter reinforcement in one component.

✓ Read this if BCBAs who use multiple schedules or alternate rich/lean tasks within a session.
✗ Skip if Clinicians working with only one schedule or who never split reinforcement rates across components.

01Research in Context

01

What this study did

Spealman (1978) worked with squirrel monkeys in a lab. The monkeys pressed levers under two alternating schedules. One schedule stayed the same. The other was switched to extinction or timeout.

The team watched what happened in the unchanged schedule. They wanted to see if stopping rewards in one part would hurt responding in the other part.

02

What they found

When rewards stopped in the changed part, response rates in the steady part dipped. This negative induction showed up fast. The dip faded after a few sessions.

The effect only appeared in monkeys. Earlier pigeon studies had seen the opposite. The paper warns that contrast effects may not cross species lines.

03

How this fits with other research

Davol et al. (1977) found you can shrink negative contrast by tweaking the schedule to skip long pauses. Spealman (1978) agrees the effect is fragile, but shows it can flip to negative if you use monkeys instead of pigeons.

Innis (1978), published the same year, saw mixed local contrast in pigeons under fixed-interval schedules. Both studies stress transient effects, yet species and schedule type change the direction.

Craig et al. (2018) later showed that off-baseline extinction in one part can weaken resistance in the other. This extends D’s core point: what happens in one component spills into the next, even without direct training.

04

Why it matters

If you run multiple schedules with clients, do not assume contrast will look the same across learners. Check for brief dips or surges right after you change reinforcement in one task. If you see a drop, wait a few sessions before adjusting; the effect may vanish on its own. And if you switch species or response forms, rerun your baseline—what helps pigeons might hurt monkeys.

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Count responses in the unchanged task for three sessions after you thin or stop rewards in the other task; note any dip and wait before making further changes.

02At a glance

Intervention
not applicable
Design
single case other
Finding
negative

03Original abstract

In Experiment I, lever pressing by squirrel monkeys was maintained under a sequence of variable-interval, multiple variable-interval variable-interval, and multiple variable-interval extinction schedules of food presentation. Negative induction (decreased responding in the unchanged component) occurred when one component of the multiple variable-interval variable-interval schedule was changed to extinction. Negative induction was transient over sessions; responding in the unchanged component usually recovered to a rate similar to that under the multiple variable-interval variable-interval schedule. Negative induction was not accompanied by consistent changes in the patterns of local responding within the unchanged component, and did not depend on whether component schedules were associated with localized (lever lights) or diffuse visual stimuli (houselights), or on whether the unchanged component was a 60- or 180-sec variable-interval schedule. In Experiment II, responding was maintained under a sequence of variable-interval and multiple variable-interval timeout schedules of food presentation. Negative induction occurred when responding declined gradually in the timeout component but not when responding declined abruptly. The nature of interactions in multiple schedules may depend on the species; negative induction was observed with squirrel monkeys under conditions similar to those that produce positive contrast with pigeons.

Journal of the experimental analysis of behavior, 1978 · doi:10.1901/jeab.1978.30-315