Effects of variations in the temporal distribution of reinforcements on interval schedule performance

Pigeons were exposed to variable-interval and fixed-interval schedules and schedules approximating variable-interval and fixed-interval schedules. The probabilities of the variable-interval and fixed-interval components in a mixed fixed-interval variable-interval schedule in Experiment I and the minimum and maximum interreinforcement intervals in Experiment II in a variable-interval schedule were manipulated to create intermediate schedule contingencies and contingencies approximating simple variable-interval or fixed-interval contingencies. Maximal control by time as defined by quantitative indices of the temporal pattern of response occurred as fixed-interval contingencies were approximated and minimal control occurred as variable-interval contingencies were approximated. Changes in the temporal pattern of response were systematically related to changes in the temporal distribution of reinforcements with both procedural definitions for manipulating the temporal distribution of reinforcements.     

Attention in the pigeon: a reevaluation

During training sessions, pigeons were successively exposed to compounds consisting of a white triangle on a red background and a white circle on a green background. Key pecking intermittently produced grain reinforcers in the presence of one form-color compound. Once key pecking was confined to the compound associated with reinforcement, the elements—red, green, triangle, and circle—were presented during a test in which no reinforcement was available. Each bird pecked nearly exclusively in the presence of the color previously associated with reinforcement, a result that might be interpreted as indicating that the subjects had attended to color, but not form during training. Pecking was next reinforced when either the triangle or the circle was present. Pecking in the presence of the form previously associated with reinforcement was acquired more rapidly. This result suggests that the birds had learned about the forms during training, and that conclusions about attention based on the lack of differential pecking in the nonreinforcement test may not be appropriate.     

Elicited responding to signals for reinforcement: the effects of overall versus local changes in reinforcement probability

Pigeons were studied on a three-component multiple schedule where all reinforcement was independent of responding. Two components were cued by different keylights and were associated with different rates of reinforcement. The third was always a no-key period associated with extinction. After a few sessions, pecking was elicited by the keylights signalling the reinforcement and continued to be maintained indefinitely. The duration and sequence of the three components were varied to determine if the primary controlling variable was differences in the overall probability of reinforcement, or if it was the immediate change in reinforcement signalled by the onset and/or offset of the stimulus. Both variables were found to control behavior. When 30-sec components were used, the primary controlling variable was the overall probability of reinforcement, but when 3-min components were used, overall probability had little effect. Control by local changes in reinforcement also occurred, although the type of local control varied both across subjects and experimental conditions. Some behaviors were controlled more by the change in reinforcement signalled by the onset of the stimulus, while others were controlled more by the change signalled by the offset of the stimulus.     

Conjunctive schedules of reinforcement: III. A fixed-interval adjusting fixed-ratio schedule

Key pecking of three pigeons was studied under a conjunctive schedule that specified both a fixed-interval and an adjusting fixed-ratio requirement. The fixed-interval schedule was 6 min for one pigeon and 3 min for the other two. The size of the ratio requirement was determined within each cycle of the fixed interval by the duration of the pause before responding began. The fixed-ratio value was at maximum at the start of each fixed interval and decreased linearly until the first response occurred (adjusting fixed-ratio schedule). A peck produced food when the number of responses remaining on the fixed-ratio schedule was completed and when the fixed interval had elapsed. If no response occurred during the interval, the fixed-ratio requirement decreased to one and a single response after the interval elapsed produced food. The initial value of the adjusting fixed-ratio schedule was studied over a range of 0 to 900. Increases in the adjusting fixed-ratio schedule to about 300 responses increased both pause duration and running response rate and also modified the pattern of responding from that obtained under the fixed-interval schedule. Higher values of the adjusting fixed ratio generally decreased pause duration and running response rate and also disrupted responding. Interreinforcement time under the conjunctive schedule was increased substantially when the adjusting fixed-ratio size exceeded 300 responses.     

Choice and foraging: the effects of accessibility on acceptability.

Pigeons responded in a successive-encounters choice procedure in which accessibility of the less profitable of two outcomes varied either in terms of probability of encounter or search time to encounter (keeping search time to the more profitable outcome constant). When the less profitable outcome was made more probable its acceptance became more likely. However, when search time to encounter the less profitable outcome was shortened, its acceptance became less likely. Both results are consistent with the delay-reduction hypothesis and with an optimality model developed for application to the successive-encounters choice procedure.     

Concurrent schedules: Interaction of reinforcer frequency and reinforcer duration

Six pigeons were trained on concurrent variable-interval schedules with unequal reinforcer durations for the two responses. The schedules arranged on the two keys were kept equal while they were varied in absolute size. As the overall reinforcer rate was increased, both response-allocation and time-allocation measures of choice showed a trend toward indifference, and measures of sensitivity to reinforcer-duration ratios significantly decreased. Recent reports have shown that the generalized matching law cannot describe the changes in behavior allocation under constant delay-, duration-, or rate-ratios when changes are made in the absolute levels of each of these variables. The present results complement these findings by demonstrating that the concatenated generalized matching law cannot describe the interactions of two reinforcer variables on behavior allocation.     

Control of behavior by an establishing stimulus

Seventeen pigeons were exposed to a three-key discrete-trial procedure in which a peck on the lit center key produced food if, and only if, the left keylight was lit. The center key was illuminated by a peck on the lit right key. Of interest was whether subjects pecked the right key before or after the response-independent onset of the left keylight. Pecks on the right key after left-keylight onset suggest control of behavior by the left keylight—an establishing stimulus. In three experiments, the strength of center-keylight onset as conditioned reinforcer for a response on the right key was manipulated by altering the size of the reduction in time to food delivery correlated with its onset. Control of pigeons' key pecks by onset of the left keylight occurred on more trials per session when the center keylight was a relatively weak conditioned reinforcer and on fewer trials per session when the center keylight was a relatively strong condtioned reinforcer. Differences across conditions in the degree of control by onset of the establishing stimulus were greatest when changes in conditioned reinforcer strength occurred relatively frequently and were signaled. The results provide evidence of the function of an establishing stimulus.     

Information on response requirements compared with information on food density as a reinforcer of observing in pigeons

On a variable-interval schedule, pecking the key to the pigeon's right (observing response) produced red or green displays relating to the delivery of grain and its dependence on pecking the key to the left (food key). During various blocks of sessions, mixed (no stimulus change) schedules including the following pairs of components were temporarily converted by the observing response to their corresponding multiple (correlated stimuli) schedules: variable-interval 60-s, extinction; variable-interval 60-s, variable-time (response-independent) 60-s; extinction, variable-time 60-s. Differences in food delivery maintained substantial rates of responding on the observing key, without regard to pecking requirements on the food key. Although stimuli correlated with differences in the response requirement on the food key maintained higher observing rates than those maintained by uncorrelated stimuli, they were much lower than those based on food. The value of predictive stimuli as reinforcers is determined by the value of the events predicted. In particular, the cost of pecking appears to be low, and this may place limitations on the applicability of energy-based and economic models of behavior.     

Absolute and relative measures of dimensional contrast.

Two sets of experiments examined the discriminative performance of pigeons on a visual flicker-rate continuum using a maintained generalization procedure. In the first experiment, responses during the intermediate stimulus value were not reinforced, whereas responses during all other stimuli were reinforced periodically. In the second experiment, training was similar to the first, with the exception of one condition in which stimuli adjacent to the negative stimulus border were eliminated from the discrimination set. Results from both experiments show that positive dimensional contrast seems to represent a relative enhancement of discrimination gradient form, rather than an absolute increase in responding with respect to prior baseline. Further, the form and magnitude of positive dimensional contrast are not predictable from the form and magnitude of baseline response rates. Results from the second experiment indicate that eliminating border stimuli increased response-rate differences between positive and negative stimuli, but did not necessarily diminish the magnitude of positive dimensional contrast.     

Determinants of pausing under variable-ratio schedules: Reinforcer magnitude, ratio size, and schedule configuration

Pigeons pecked a key under two-component multiple variable-ratio schedules that offered 8-s or 2-s access to grain. Phase 1 assessed the effects of differences in reinforcer magnitude on postreinforcement pausing, as a function of ratio size. In Phase 2, postreinforcement pausing and the first five interresponse times in each ratio were measured as a function of differences in reinforcer magnitude under equal variable-ratio schedules consisting of different configurations of individual ratios. Rates were also calculated exclusive of postreinforcement pause times in both phases. The results from Phase 1 showed that as ratio size increased, the differences in pausing educed by unequal reinforcer magnitudes also increased. The results of Phase 2 showed that the effects of reinforcer magnitude on pausing and IRT durations were a function of schedule configuration. Under one configuration, in which the smallest ratio was a fixed-ratio 1, pauses were unaffected by magnitude but the first five interresponse times were affected. Under the other configuration, in which the smallest ratio was a fixed-ratio 7, pauses were affected by reinforcer magnitude but the first five interresponse times were not. The effect of each configuration seemed to be determined by the value of the smallest individual ratio. Rates calculated exclusive of postreinforcement pause times were, in general, directly related to reinforcer magnitude, and the relation was shown to be a function of schedule configuration.