Positive and negative contrast as a function of component duration for key pecking and treadle pressing

Pigeons responded on several multiple schedules for food reinforcers. The duration of the components varied from four seconds to 16 minutes. The absolute size of positive (Experiment 1) and negative (Experiment 2) behavioral contrast varied inversely with component duration when key pecks produced the reinforcers. The absolute size of negative contrast varied directly with component duration, when treadle presses produced the reinforcers (Experiment 3). These results conform to theories that suggest that positive and negative contrast are symmetrical when pigeons peck keys. They also conform to theories that suggest that the same principles do not govern contrast when pigeons peck keys as when they press treadles. Finally, the results support the measurement of behavioral contrast by the differences between baseline rates of responding and the rates emitted when contrast is present.     

Changeover delay effects on topographically tagged discriminative behavior

In a multiple variable-interval extinction schedule, pigeons' responses on an operant key were differentially reinforced in the presence of discriminative stimuli located on a signal key. Changeover delays of zero, one, two, or four seconds specified the time following a signal-key response within which an operant-key response was not reinforced. Systematic reduction of signal-key response rates with increasing changeover-delay duration indicated that signal-key responding was largely maintained by reinforcement of adventitious signal-key/operant-key response chains.     

Response requirements as constraints on output

Two experiments studied how added response requirements affected fixed-interval schedule performance. Experiment 1 involved tandem fixed-interval fixed-ratio schedules, and Experiment 2 studied conjunctive fixed-interval fixed-ratio schedules. In both, pigeons' output, defined as overall response rate or as responses during the interval, first increased and then decreased as the ratio was raised. With small ratio requirements, the frequency of reinforcement in time either did not change or decreased slightly. With progressively larger ratios, reinforcement frequency decreased consistently. Alternative explanations were discussed. The first, a reinforcement theory account, was that response strength is an increasing monotonic function of both the response requirement and reinforcement frequency, and the bitonic output function represents interacting effects. Increases in the response requirement accompanied by small changes in reinforcement frequency enhance output, but further increases result in large enough decrements in reinforcement frequency so that output is lowered. The second explanation does not view reinforcement as a basic process but, instead, derives from concepts of economics and conservation. Organisms allocate their behavior among alternatives so as to maximize value, where value is a function of the responses that can occur in a given situation under the set of restrictions imposed by particular schedules. One form of this theory explicitly predicts that output is a bitonic function of ratio requirements in simple ratio schedules. However, it was not clear that this model could explain the present effects involving joint ratio and interval schedule restrictions.     

Choice and number of reinforcers

Pigeons were exposed to the concurrent-chains procedure in two experiments designed to investigate the effects of unequal numbers of reinforcers on choice. In Experiment 1, the pigeons were indifferent between long and short durations of access to variable-interval schedules of equal reinforcement density, but preferred a short high-density terminal link over a longer, lower density terminal link, even though in both sets of comparisons there were many more reinforcers per cycle in the longer terminal link. In Experiment 2, the pigeons preferred five reinforcers, the first of which was available after 30 sec, over a single reinforcer available at 30 sec, but only when the local interval between successive reinforcers was short. The pigeons were indifferent when this local interval was sufficiently long. The pigeons' behavior appeared to be under the control of local terminal-link variables, such as the intervals to the first reinforcer and between successive reinforcers, and was not well described in terms of transformed delays of reinforcement or reductions in average delay to reinforcement.     

Free-operant choice behavior: A molecular analysis

Pigeons' pecks to two concurrent initial-link stimuli occasionally produced one of two mutually exclusive terminal links. Further responding to the terminal-link stimulus produced food under fixed-interval or fixed-ratio schedules. In such concurrent chained schedules, investigators rarely use a changeover delay to control superstitious switching, although it is customary to use a changeover delay in simple concurrent schedules in which choice responses produce food directly. When terminal-link fixed-interval schedules were equal or similar in duration and no changeover delay was employed, conditional probabilities of choice for a schedule were found to be lower if the last choice was for that schedule than if the last choice was for the other schedule (“switching dependency”). Imposition of a changeover delay with equal or unequal terminal links produced the opposite pattern: conditional probabilities of choice for a schedule were higher if the last choice was for that schedule than if the last choice was for the other schedule. Turning off all chamber lights during the changeover delay interval attenuated these “repetition dependencies.” The results indicate that excessive switching can complicate the interpretation of data from concurrent chains much as from simple concurrent schedules, and that using blackouts to control switching may be preferable to using a changeover delay.     

DEVIATIONS FROM MATCHING AS A MEASURE OF PREFERENCE FOR ALTERNATIVES IN PIGEONS

Preferences for larger or smaller formally defined response classes were investigated in a concurrent schedule procedure. 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. Systematic shifts in function intercepts in the former group indicate a response bias toward the response-constrained (single-key) schedule alternative. Although contrary to the literature of preference for choice, this finding may be interpretable through an account dealing with imposed variability of responding.     

Interresponse-time shaping by variable-interval-like interresponse-time reinforcement contingencies

The interresponse-time reinforcement contingencies and distributions of interreinforcement intervals characteristic of certain variable-interval schedules were mimicked by reinforcing each key peck with a probability equal to the duration of the interresponse time it terminated, divided by the scheduled mean interreinforcement interval. The interresponse-time reinforcement contingency was then eliminated by basing the probability of reinforcement on the fifth interresponse time preceding the key peck. Even though distributions of interreinforcement intervals were unaffected by this manipulation, response rates consistently increased. A second experiment replicated this effect and showed it to combine additively with that of mean reinforcement rate. These results provide strong support for the contention that current analyses of variable-interval response rates that ignore the inherent interresponse-time reinforcement contingency may be seriously in error.     

Transfer of pigeons' matching to sample to novel sample locations

This study examined the conditions under which conditional stimulus control by the sample stimuli in three-key matching-to-sample paradigms would generalize across the different possible sample locations. In Experiments 1 and 2, the samples appeared on the left and right side keys during initial training and then on the center key during testing. Transfer of pigeons' matching performances to the center-key samples was evident after both identity and symbolic matching training. In Experiment 3, pigeons trained on symbolic matching with two side-key samples or with a side-key and a center-key sample generally transferred their learned matching performances to those samples when they subsequently appeared in the remaining (novel) location. These results indicate that, when two-choice conditional discriminations are learned with more than one sample location, the visual characteristics of the sample per se predominantly come to control the pigeons' comparison choices. This finding encourages the use of the multiple-location training procedure as a way of reducing control by location, thus providing a more discriminating test of symmetry in animals.