Effects of reinforcer duration on responding in two-link chained interval schedules

Each of five pigeons was exposed to two or more durations of access to mixed grains on two-link, chained, interval schedules in which both links were identical fixed-interval or variable-interval schedules. Response rates were an increasing function of reinforcer duration for both initial and terminal links. For both types of interval schedules, initial-link response rates were more sensitive to reinforcer duration than were terminal-link response rates. The present results, together with prior ones, suggest that chaining and choice procedures are each sufficient for demonstrating substantial sensitivity of responding to changes in reinforcer duration.     

The influence of "preparedness" on autoshaping, schedule performance, and choice.

Two groups of experimentally naive pigeons were exposed to an autoshaping procedure in which the response key was mounted on the wall (the conventional location) or on the floor of the chamber. In two experiments, subjects readily responded to the wall key, but floor-key subjects required shaping. A subsequent experiment compared performance of wall- and floor-key groups on an ascending series of fixed-ratio schedule values, resistance to extinction, differential reinforcement of other behavior, and reversal of key assignment. Each experiment was followed by several sessions of fixed-ratio training; the performance of the wall- and floor-key groups was almost identical throughout. In the final experiment, a fixed-ratio requirement could be completed on either or both keys. Birds initially chose the key on which they had responded during the preceding (reversal of key assignment) experiment. However, within a few sessions both groups showed almost exclusive preference for the floor key. Preference for a key located on the floor may follow from the fact that pigeons are ground feeders and may thus be more "prepared" to peck the floor than to peck a wall. However, autoshaping, under the conditions prevailing here, occurred much more readily to the wall key, suggesting that pecking a vertical surface is more highly prepared. Difficulties in determining relative preparedness seem moot, however, given the lack of between-group differences in the intervening experiments. It is thus unlikely that schedule performances critically depend upon the specific operant response involved.     

Effects Of Histories Of Differential Reinforcement Of Response Rate On Variable-interval Responding

Three pigeons were exposed first to multiple differential-reinforcement-of-high-rate and differential-reinforcement-of-low-rate schedules that were correlated with green and red keys, respectively, and then were shifted to a variable-interval schedule arranged on a white key. In subsequent test sessions, the variable-interval schedule continued to operate, but green and red keys replaced the white key in alternate sessions. In Part 1 of the experiment, the variable-interval schedule correlated with the white key was introduced immediately after the multiple-schedule condition, and the test condition began 15 days later. This sequence was repeated twice, with a reversal of the correlation of the key colors with the components of the multiple schedule at the start of each new cycle. Part 2 added a 6-month break between the multiple-schedule history and the white-key variable-interval schedule followed by test sessions. The procedure was then repeated with a reversal of the correlation between key colors and multiple-schedule components. In the test sessions of Part 1, all pigeons consistently responded faster in the presence of the key color most recently correlated with the differential-reinforcement-of-high-rate contingency than during the color most recently correlated with the differential-reinforcement-of-low-rate contingency. Similar but smaller effects were observed in Part 2. The effects of the reversals in these two parts of the experiment showed that only the most recent contingency exerted an influence on subsequent responding. The data suggest that this effect of the most recent history continues to operate on behavior under current contingencies even after a long lapse of time.     

Effects of concurrent response-independent reinforcement on fixed-interval schedule performance

In three experiments, behavior maintained by fixed-interval schedules changed when response-independent reinforcement was delivered concurrently according to fixed- or variable-time schedules. In Experiment I, a pattern of positively accelerated responding during fixed interval was changed to a linear pattern when response-independent reinforcement occurred under a variable-time schedule. Overall response rates (total responses/total time) decreased as the frequency of response-independent reinforcement increased. Experiment II showed that the response-rate changes in the first experiment were controlled by the response-reinforcer relation, but the changes in patterns of responding were similar whether concurrently available reinforcement at varying times was response-dependent or response-independent. In the final experiment, the addition of response-independent reinforcement at fixed times to a fixed-interval schedule resulted in changes in both local and overall response rates and in the occurrence of positively accelerated responding between reinforcements. These results suggest that the temporal distribution of reinforcers determines response patterns and that both the response-reinforcement dependency and the schedule of reinforcement determine overall response rates during concurrently scheduled response-dependent and response-independent reinforcement.     

Concurrent-schedule performance in transition: changeover delays and signaled reinforcer ratios

Six pigeons were trained in experimental sessions that arranged six or seven components with various concurrent-schedule reinforcer ratios associated with each. The order of the components was determined randomly without replacement. Components lasted until the pigeons had received 10 reinforcers, and were separated by 10-s blackout periods. The component reinforcer ratios arranged in most conditions were 27:1, 9:1, 3:1, 1:1, 1:3, 1:9 and 1:27; in others, there were only six components, three of 27:1 and three of 1:27. In some conditions, each reinforcement ratio was signaled by a different red-yellow flash frequency, with the frequency perfectly correlated with the reinforcer ratio. Additionally, a changeover delay was arranged in some conditions, and no changeover delay in others. When component reinforcer ratios were signaled, sensitivity to reinforcement values increased from around 0.40 before the first reinforcer in a component to around 0.80 before the 10th reinforcer. When reinforcer ratios were not signaled, sensitivities typically increased from zero to around 0.40. Sensitivity to reinforcement was around 0.20 lower in no-changeover-delay conditions than in changeover-delay conditions, but increased in the former after exposure to changeover delays. Local analyses showed that preference was extreme towards the reinforced alternative for the first 25 s after reinforcement in changeover-delay conditions regardless of whether components were signaled or not. In no-changeover-delay conditions, preference following reinforcers was either absent, or, following exposure to changeover delays, small. Reinforcers have both local and long-term effects on preference. The former, but not the latter, is strongly affected by the presence of a changeover delay. Stimulus control may be more closely associated with longer-term, more molar, reinforcer effects.     

Effects of cocaine and d-amphetamine on the repeated acquisition and performance of conditional discriminations.

The acute and chronic effects of cocaine and d-amphetamine on food-reinforced behavior were investigated in pigeons responding on a two-component multiple schedule. In one component, the behavioral task consisted of the same chain of conditional discriminations each session (performance). In the other component, the chain of conditional discriminations was changed from session to session (learning). In comparison to control sessions, both acute cocaine and d-amphetamine increased errors in each component of the multiple schedule. Responding in the learning component, however, was generally disrupted at lower doses than those that affected responding in the performance component. At high doses, both drugs produced pauses in responding in each component in three of the four subjects. Pausing engendered by d-amphetamine was approximately twice as long as that under cocaine. Upon chronic administration, both the pausing and error-increasing effects of each drug diminished. Drug-induced changes in timeout responding, however, did not decrease during chronic administration. Redeterminations of the d-amphetamine dose-effect curves following chronic cocaine administration suggested the existence of cross-tolerance between cocaine and d-amphetamine. Both the acute and chronic data are consistent with the view that conditions of stimulus control may modulate the behavioral effects of drugs.     

Temporal factors influencing the pigeon's successive matching-to-sample performance: sample duration, intertrial interval, and retention interval

A successive matching-to-sample procedure that entails the sequential presentation of sample and test stimuli and the monitoring of response rates in a go/no-go discrimination of matching and nonmatching stimuli was studied as an alternative to the familiar delayed-matching paradigm of animal short-term memory. Three within-subject experiments studied the effects of sample duration (1 to 12 seconds), intertrial interval (5 to 50 seconds), and retention interval (1 to 50 seconds) on the pigeon's successive-matching performance. The results revealed that retention was (a) an increasing function of sample duration and intertrial interval, and (b) a decreasing function of retention interval. These results were in accord with those of more traditional short-term memory paradigms, and reveal the suitability of the successive-matching procedure for studying memory processes.     

Performances on ratio and interval schedules of reinforcement: Data and theory

Two differences between ratio and interval performance are well known: (a) Higher rates occur on ratio schedules, and (b) ratio schedules are unable to maintain responding at low rates of reinforcement (ratio “strain”). A third phenomenon, a downturn in response rate at the highest rates of reinforcement, is well documented for ratio schedules and is predicted for interval schedules. Pigeons were exposed to multiple variable-ratio variable-interval schedules in which the intervals generated in the variable-ratio component were programmed in the variable-interval component, thereby “yoking” or approximately matching reinforcement in the two components. The full range of ratio performances was studied, from strained to continuous reinforcement. In addition to the expected phenomena, a new phenomenon was observed: an upturn in variable-interval response rate in the midrange of rates of reinforcement that brought response rates on the two schedules to equality before the downturn at the highest rates of reinforcement. When the average response rate was corrected by eliminating pausing after reinforcement, the downturn in response rate vanished, leaving a strictly monotonic performance curve. This apparent functional independence of the postreinforcement pause and the qualitative shift in response implied by the upturn in variable-interval response rate suggest that theoretical accounts will require thinking of behavior as partitioned among at least three categories, and probably four: postreinforcement activity, other unprogrammed activity, ratio-typical operant behavior, and interval-typical operant behavior.     

Stimulus effects on concurrent performance in transition

Six experimentally naive pigeons were exposed to concurrent variable-interval variable-interval schedules in a three-key procedure in which food reinforcement followed pecks on the side keys and pecks on the center key served as changeover responses. In Phase 1, 3 birds were exposed to 20 combinations of five variable-interval values, with each variable-interval value consistently associated with a different color on the side keys. Another 3 pigeons were exposed to the same 20 conditions, but with a more standard procedure that used a nondifferential discriminative stimulus on the two side keys throughout all conditions. In Phase 2, the differential and nondifferential stimulus conditions were reversed for each pigeon. Each condition lasted for one 5-hr session and one subsequent 1-hr session. In the last 14 conditions of each phase, the presence of differential discriminative stimuli decreased the time necessary for differential responding to develop and increased the sensitivity of behavior to reinforcement distribution in the 1st hr of training; during the last hours of training in each condition, however, the effects of the differential discriminative stimuli could not be distinguished from the effects of reinforcement distribution per se. These results show the importance of studying transitions in behavior as well as final performance. They may also be relevant to discrepancies in the results of previous experiments that have used nonhuman and human subjects.     

Tolerance to effects of cocaine on behavior under a response-initiated fixed-interval schedule

Tolerance to effects of cocaine can be modulated by schedules of reinforcement. With multiple ratio schedules, research has shown an inverse relationship between ratio requirement and amount of tolerance that resulted from daily administration of the drug. In contrast, tolerance to the effects of cocaine on behavior under multiple interval schedules generally has developed regardless of interval value. Under interval schedules reinforcement depends on the animal making one response following a time interval. Thus, as time to respond increases, the time to reinforcement decreases. On the other hand, fixed ratio schedules require a specified number of responses to be made prior to reinforcement. Therefore, delaying the initiation of responding does not coincide with a significant decrease in the time to reinforcement. In the current experiment, 6 pigeons were trained to respond under a three-component multiple schedule, with a different tandem fixed-ratio 1 fixed-interval schedule in each component. The multiple schedule required one response, which was followed by one of three fixed-interval values (5, 15, or 60 s). Thus, the multiple schedule was interval-like because after the fixed-ratio 1, only one more response was required for reinforcement, but it was also ratio-like because the length of the pause at the beginning of each interreinforcer interval affected the time until the next reinforcer. Acute administration of cocaine generally resulted in dose-dependent decreases in responding. Chronic (i.e., daily) administration of a rate-decreasing dose resulted in tolerance patterns similar to those usually obtained with multiple ratio schedules. That is, the magnitude of tolerance was related inversely to schedule size. These results suggest that delay to reinforcement from the initial response may play a role in the development of schedule-parameter-related tolerance.     

Signalled and unsignalled percentage reinforcement of performance under a chained schedule

Pigeons were trained to peck a key under a chained fixed-ratio 15 fixed-interval 25-sec schedule of food presentation. In Experiment 1, blocks of sessions in which 100%, 75%, 50%, and 25% of the sequences ended with food presentation were conducted. When food presentation was omitted, a timeout of equal duration replaced it. As the frequency of food presentation decreased so did the frequency of completing the chained schedule. In Experiment 2, 75%, 50%, or 25% of the sequences terminated with food presentation and outcomes were signalled, i.e., completion of the fixed ratio resulted in either a stimulus correlated with the fixed-interval 25-sec schedule or a stimulus correlated with extinction. As the frequency of food presentation decreased, the number of sequences completed per session increased for two pigeons and remained high for a third. In Experiments 3 and 4, assessments of the effects of signalling the outcome of the chained schedule were made with response-independent presentation of events at the end of the sequence. Again, signalling the outcome of the chained schedule led to more chains being completed per session than did not signalling the outcome. Stimuli differentially paired with food presentation have powerful behavioral effects that may be attributed to the potency of these stimuli as conditioned reinforcers.     

Variable-interval schedule performance in open and closed economies

In two experiments, pigeons obtained food according to variable-interval schedules. In the first experiment, equivalent variable-interval schedules with average interreinforcer intervals ranging between 10 and 80 s in different conditions were studied in both open and closed economies. Response rates increased as reinforcement frequency decreased in the closed economy. By contrast, in the open economy response rates decreased for 1 bird and were variable for the other as reinforcement frequency decreased. The second experiment showed that the differences in the functions between responding and reinforcement frequency in the two types of economies were not due to changes in deprivation level. These results suggest that open and closed economies yield different behavioral effects. This conclusion is supported further by a reconsideration of previous findings that appear counter to the conclusion.     

Effects of methadone on alternative fixed-ratio fixed-interval performance: latent influences on schedule-controlled responding.

Effects of methadone on pigeons' key pecking were examined under four conditions selected to analyze the control of behavior under alternative fixed-ratio fixed-interval schedules. In Condition 1, pigeons pecked under one of three different alternative schedules (alternative fixed-ratio 50 fixed-interval 90 s, alternative fixed-ratio 75 fixed-interval 90 s and alternative fixed-ratio 200 fixed-interval 90 s) each week. In Condition 2, fixed-ratio 50 or fixed-ratio 75 schedules were in effect during baseline sessions, and alternative fixed-ratio 50 fixed-interval 90-s or alternative fixed-ratio 75 fixed-interval 90-s schedules were in effect during sessions in which methadone was administered. In Condition 3, effects of methadone on key pecking maintained under fixed-ratio 50 and fixed-ratio 75 schedules were examined, whereas in Condition 4 the effects of methadone on key pecking under a fixed-interval 90-s schedule as well as fixed-ratio 50 and fixed-ratio 75 schedules were investigated. Control by the fixed-interval contingency was assessed by computing the proportion of total session reinforcers delivered under the fixed-interval schedule. Methadone administration (0.5-4.0 mg/kg) shifted the predominant source of schedule control under the alternative schedule from the fixed-ratio schedule to the fixed-interval contingency. This shift was dependent on methadone dose and fixed-ratio size. Control by the fixed-interval contingency was greatest following extensive exposure to the interval component embedded within the alternative schedule (Condition 1), but was apparent to a lesser degree with even very limited exposure to the alternative fixed-ratio fixed-interval schedule (Condition 2). Interreinforcement intervals comparable to those under fixed-interval schedule were not observed under the fixed-ratio schedules presented alone (Condition 3). Repeated exposure to the fixed-interval contingency outside the context of the alternative fixed-ratio fixed-interval schedule did not engender performance changes under a fixed-ratio schedule which would mimic those of increased fixed-interval contingency control (Condition 4). These data suggest that drug administration can be used to unmask the influence of contingencies that are latent under baseline conditions and reveal influences of both past and present environmental variables.     

Waiting in pigeons: the effects of daily intercalation on temporal discrimination.

Pigeons trained on cyclic-interval schedules adjust their postfood pause from interval to interval within each experimental session. But on regular fixed-interval schedules, many sessions at a given parameter value are usually necessary before the typical fixed-interval "scallop" appears. In the first case, temporal control appears to act from one interfood interval to the next; in the second, it appears to act over hundreds of interfood intervals. The present experiments look at the intermediate case: daily variation in schedule parameters. In Experiments 1 and 2 we show that pauses proportional to interfood interval develop on short-valued response-initiated-delay schedules when parameters are changed daily, that additional experience under this regimen leads to little further improvement, and that pauses usually change as soon as the schedule parameter is changed. Experiment 3 demonstrates identical waiting behavior on fixed-interval and response-initiated-delay schedules when the food delays are short (less than 20 s) and conditions are changed daily. In Experiment 4 we show that daily intercalation prevents temporal control when interfood intervals are longer (25 to 60 s). The results of Experiment 5 suggest that downshifts in interfood interval produce more rapid waiting-time adjustments than upshifts. These and other results suggest that the effects of short interfood intervals seem to be more persistent than those of long intervals.     

Stimulus Effects On Behavior Allocation In Three-alternative Choice

Six pigeons were trained on three-alternative concurrent variable-interval schedules that were available through a switching response and were signaled by colored stimuli. The discriminative stimuli for two of the schedules were always 560 nm and 630 nm, but the stimulus signaling the third alternative was varied across conditions over seven levels between these colors. For each third-alternative stimulus condition, the relative frequency of reinforcers was varied over three conditions with 4:1 and 16:1 reinforcer ratios between each pair of alternatives. The distribution of responses between the alternatives was dependent jointly on the third-alternative reinforcer rate and on the disparity between the stimulus signaling the third alternative and those signaling the other alternatives. A generalized matching approach was unable to provide invariant measures of the discriminability between constant stimuli, but a contingency-discriminability approach provided excellent fits and sensible and invariant stimulus discriminability measures.     

Effects of cocaine on performance under fixed-interval schedules with a small tandem ratio requirement

Daily administration of cocaine often results in the development of tolerance to its effects on responding maintained by fixed-ratio schedules. Such effects have been observed to be greater when the ratio value is small, whereas less or no tolerance has been observed at large ratio values. Similar schedule-parameter-dependent tolerance, however, has not been observed with fixed-interval schedules arranging comparable interreinforcement intervals. This experiment examined the possibility that differences in rate and temporal patterning between the two types of schedule are responsible for the differences in observed patterns of tolerance. Five pigeons were trained to key peck on a three-component multiple (tandem fixed-interval fixed-ratio) schedule. The interval values were 10, 30, and 120 s; the tandem ratio was held constant at five responses. Performance appeared more like that observed under fixed-ratio schedules than fixed-interval schedules. Effects of various doses of cocaine given weekly were then determined for each pigeon. A dose that reduced responding was administered prior to each session for 50 days. A reassessment of effects of the range of doses revealed tolerance. The degree of tolerance was similar across components of the multiple schedule. Next, the saline vehicle was administered prior to each session for 50 days to assess the persistence of tolerance. Tolerance diminished in all subjects. Overall, the results suggested that schedule-parameter-dependent tolerance does not depend on the temporal pattern of responding engendered by fixed-ratio schedules.     

Fixed-interval performance: The dynamics of behavior and the interval length

Postreinforcement pauses from successive intervals under various fixed-interval schedules (ranging from 15 seconds to 480 seconds in length) were subjected to lag-1 autocorrelation analysis. Results from both rats and pigeons suggested that there was a consistent tendency for pause values in successive intervals to be weakly positively related. This tendency did not appear to change systematically with interval length and was exhibited both when the reinforcer magnitude was constant and when it was variable at different interval values. The findings do not support suggestions that the dynamic properties of performance under fixed-interval schedules vary systematically with interval length, and are in the opposite direction from some previous findings suggesting that measures of behavior (such as post-reinforcement pause length or number of responses) in successive intervals are inversely related.     

Effects of varying stimulus disparity and the reinforcer ratio in concurrent-schedule and signal-detection procedures.

The present study measured the effects of stimulus and reinforcer variations on pigeons' behavior in two different choice procedures. Two intensities of white light were presented as the stimuli on the main key in a switching-key concurrent schedule and as the sample stimuli in a signal-detection procedure. Under both procedures, the scheduled rate of reinforcement was varied across conditions to produce various ratios of obtained reinforcement. These ratios were obtained for seven pairs of light intensities. In the concurrent schedules, the effects of reinforcer-ratio variations were positively correlated with the physical disparity between the two light intensities. In the signal-detection procedure, changes in the reinforcer ratio produced greater effects on performance when stimulus disparity was very low or very high compared to those found at intermediate levels of stimulus disparity. This discrepancy creates a dilemma for existing behavioral models of signal-detection performance.