Deviations from matching as a measure of preference for alternatives in pigeons.
Tacking a non-paying key onto one alternative keeps matching intact in pigeons.
01Research in Context
What this study did
Researchers gave pigeons two choices of keys to peck. One choice had two keys side-by-side. Only one of those two paid off with grain. The other choice had just one key that always paid.
They wanted to know if the useless second key would wreck the birds’ usual matching pattern. Would birds still peck in the same ratio as the grain they got?
What they found
The extra dead key did nothing. The birds kept pecking so their responses matched the grain rate, just like before.
Adding a key that never pays does not bend the matching law.
How this fits with other research
Glover et al. (1976) saw big swings away from matching when they cut all payoff for one key. The difference: they removed payoff from the whole alternative, not just tacked on an extra key. That explains the seeming clash.
Hastings et al. (2001) later showed that bigger grain pieces also leave matching untouched. Together the two papers say matching stays steady even when you tweak non-rate factors.
Shimp (1967) already proved matching can survive without maximizing. White (1979) adds another boundary: it also survives pointless keys.
Why it matters
When you set up concurrent schedules for kids or clients, extra toys or buttons that never pay off won’t distort the rate-based choice pattern. You can safely add neutral stimuli without re-balancing reinforcer rates.
Want CEUs on This Topic?
The ABA Clubhouse has 60+ free CEUs — live every Wednesday. Ethics, supervision & clinical topics.
Join Free →Leave unused icons or toys on screen during a concurrent-schedule reinforcer assessment; collect data as usual.
02At a glance
03Original abstract
Preferences for larger or smaller defined response classes were investigated in a concurrent schedule precedure. Twelve pigeons were run on a series of concurrent variable-interval reinforcement schedules, from which baseline matching functions were obtained. An experimental phase followed, in which a second response key was available in one concurrent schedule alternative. For half the birds, the second key was programmed identically with the first; for the other half, the added key was programmed for extinction, with position irrelevant. Comparison of baseline and experimental matching functions revealed no systematic changes in either slope or intercept for birds in the latter group.
Journal of the experimental analysis of behavior, 1979 · doi:10.1901/jeab.1979.32-1