On the effects of component durations and component reinforcement rates in multiple schedules

Four experiments, each using the same six pigeons, investigated the effects of varying component durations and component reinforcement rates in multiple variable-interval schedules. Experiment 1 used unequal component durations in which one component was five times the duration of the other, and the shorter component was varied over conditions from 120 seconds to 5 seconds. The schedules were varied over five values for each pair of component durations. Sensitivity to reinforcement rate changes was the same at all component durations. In Experiment 2, both component durations were 5 seconds, and the schedules were again varied using both one and two response keys. Sensitivity to reinforcement was not different from the values found in Experiment 1. In Experiment 3, various manipulations, including body-weight changes, reinforcer duration changes, blackouts, hopper lights correlated with keylights, and overall reinforcement rate changes were carried out. No reliable increase in reinforcement sensitivity resulted from any manipulation. Finally, in Experiment 4, reinforcement rates in the two components were kept constant and unequal, and the component durations were varied. Shorter components produced significantly increased response rates normally in the higher reinforcement rate component, but schedule reversals at short component durations eliminated the response rate increases. The effects of component duration on multiple schedule performance cannot be interpreted as changing sensitivity to reinforcement nor to changing bias.     

Punishment-specific effects of pentobarbital: dependency on the type of punisher.

Pigeons were trained to peck a key under a multiple random-interval 1-minute, random-interval 6-minute schedule of food presentation. Subsequently, over three phases, additions were made during the random-interval 1-minute component as follows: pecks during the component occasionally were punished by timeout presentation (Phase 1), timeouts were presented independently of responding during the component (Phase 2), pecks during the component occasionally were punished by electric-shock presentation (Phase 3). In Phases 1 and 3, response-dependent timeout and shock suppressed responding and established equivalent rates in both components of the multiple schedule. Intermediate doses of pentobarbital increased responding suppressed by electric-shock punishment but had little or no effect on responding suppressed by timeout punishment. Response-independent presentation of timeouts did not result in suppression of responding (thus showing that response-dependent timeout acted as a punisher), and pentobarbital did not reliably increase unpunished responding. Pentobarbital's selective "punishment-attenuating" properties depend on the nature of the punisher.     

Within-subject testing of the signaled-reinforcement effect on operant responding as measured by response rate and resistance to change

Response rates under random-interval schedules are lower when a brief (500 ms) signal accompanies reinforcement than when there is no signal. The present study examined this signaled-reinforcement effect and its relation to resistance to change. In Experiment 1, rats responded on a multiple random-interval 60-s random-interval 60-s schedule, with signaled reinforcement in only one component. Response resistance to alternative reinforcement, prefeeding, and extinction was compared between these components. Lower response rates, and greater resistance to change, occurred in the component with the reinforcement signal. In Experiment 2, response rates and resistance to change were compared after training on a multiple random-interval 60-s random-interval 60-s schedule in which reinforcer delivery was unsignaled in one component and a response-produced uncorrelated stimulus was presented in the other component. Higher response rates and greater resistance to change occurred with the uncorrelated stimulus. These results highlight the significance of considering the effects of an uncorrelated signal when used as a control condition, and challenge accounts of resistance to change that depend solely on reinforcer rate.     

Behavioral contrast as differential time allocation

In Experiment I, hooded rats were exposed to multiple variable-interval schedules of reinforcement in which manipulanda and reinforcement magazines at opposite ends of the experimental chamber were associated with the different components. Time allocated to each component was measured by recording the time spent by the subject in the appropriate half of the chamber. Positive behavioral contrast was observed for the comparison between multiple variable-interval 30-second variable-interval 30-second and multiple variable-interval 30-second variable-interval 90-second conditions for both response frequency and time allocation measures, but not for mean local response rate (response frequency per time allocated to a component). In Experiment II, rats were exposed to multiple variable-time schedules in which reinforcement was response independent. Time allocated to each component was measured for two conditions, multiple variable-time 30-second variable-time 30-second and multiple variable-time 30-second variable-time 90-second. Positive behavioral contrast of time allocation was exhibited. The results indicated that time allocation was differentially sensitive to changes in reinforcement probability, and that behavioral contrast may result from the differential allocation of time to the different components of the multiple schedule.     

Positive behavioral contrast in 3-month-old infants on multiple conjugate reinforcement schedules.

Positive behavioral contrast was assessed in two experiments with young infants using multiple conjugate reinforcement schedules. Reinforcement was produced by footkicks which activated the objects of an overhead crib mobile in a manner proportional to the vigor and rate of responding. Distinctive color/pattern cues on the sides of the objects served as discriminative stimuli for components of the multiple schedule. In Experiment 1, infants were trained with one cue (S+) only before insertion of S+ into a multiple schedule with an extinction component. A control group received S+ throughout all sessions. In Experiment 2, a multiple schedule was introduced at the outset, and responses in both components were reinforced before the introduction of extinction in the second component. In a final phase, reinforcement was reintroduced into the second component. Positive behavioral contrast occurred in both experiments. Response reduction in the extinction component was seen only in individual relative response curves. In both experiments, negative emotional behaviors accompanied the extinction component, and in Experiment 1, cooing accompanied presentations of S+.     

Sensitivity of time allocation to an overall reinforcer rate feedback function in concurrent interval schedules

Six pigeons were trained on concurrent variable-interval schedules in which feedback functions arranged that the overall reinforcer rate either (a) was independent of preference, (b) decreased with increasing absolute preference, or (c) increased with increasing absolute preference. In Experiment 1, the reinforcer rate in an interreinforcement interval was determined by the absolute time-allocation ratio in the previous interval. When arranged reinforcer ratios were varied, there was no evidence of control over preference by overall reinforcer rate. In Experiment 2, the feedback function arranged that reinforcer rates were an inverse function of absolute preference, and window durations were fixed times. In Phase 1, using schedules that provided a four-to-one reinforcer ratio, the window duration was decreased from 20 s to 5 s over four conditions. Then, in Phases 2 and 3, the arranged reinforcer ratios were varied. In Phase 2, the reinforcer rate in the current 5-s time window was determined by preference in the previous 5-s window, and in Phase 3, the window durations were 20 s. Again, there was no indication of control by obtained overall reinforcer rate. These data call into question theories that suggest that the process underlying matching is one of maximizing overall reinforcer rates, or that preference in concurrent aperiodic schedules is controlled to any extent by overall reinforcer rate. They also question the notion that concurrent-schedule preference is controlled by molecular maximizing.     

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.     

Effects of reinforcement rate and delay on the acquisition of lever pressing by rats.

The acquisition of lever pressing by naive rats, in the absence of shaping, was studied as a function of different rates and unsignaled delays of reinforcement. Groups of 3 rats were each exposed to tandem schedules that differed in either the first or the second component. First-component schedules were either continuous reinforcement or random-interval 15, 30, 60 or 120 s; second-component schedules were fixed-time 0, 1, 3, 6, 12, or 24 s. Rate of responding was low under continuous immediate reinforcement and higher under random-interval 15 s. Random interval 30-s and 60-s schedules produced lower rates that were similar to each other. Random-interval 120 s controlled the lowest rate in the immediate-reinforcement condition. Adding a constant 12-s delay to each of the first-component schedule parameters controlled lower response rates that did not vary systematically with reinforcement rate. The continuous and random-interval 60-s schedules of immediate reinforcement controlled higher global and first-component response rates than did the same schedules combined with longer delays, and first-component rates showed some graded effects of delay duration. In addition, the same schedules controlled higher second-component response rates in combination with a 1-s delay than in combination with longer delays. These results were related to those from previous studies on acquisition with delayed reinforcement as well as to those from similar reinforcement procedures used during steady-state responding.     

Behaviour of rats in multiple schedules of response-contingent and response-independent food presentation

During Phase I, three rats were exposed to two-component multiple schedules of response-independent food presentation. Low rates of lever-pressing were observed, and response rates in one component did not increase when food presentation was withheld in the other component. During Phase II, the same rats were exposed to two-component multiple schedules of response-contingent reinforcement. Much higher rates of lever-pressing were observed. Moreover, when reinforcement was withheld in one component, response rates in the other component increased (positive contrast), and when reinforcement was reinstated in the changed component, response rates in the other component declined (negative contrast). During Phase III, when food was again delivered independently of responding, the response rates declined again to low levels. These results indicate that the occurrence of non-instrumental lever-pressing is not a prerequisite for the occurrence of behavioural contrast in the rat, and thus cast doubt on the general applicability of the autoshaping theory of behavioural contrast     

Variable-ratio versus variable-interval schedules: response rate, resistance to change, and preference

Two experiments asked whether resistance to change depended on variable-ratio as opposed to variable-interval contingencies of reinforcement and the different response rates they establish. In Experiment 1, pigeons were trained on multiple random-ratio random-interval schedules with equated reinforcer rates. Baseline response rates were disrupted by intercomponent food, extinction, and prefeeding. Resistance to change relative to baseline was greater in the interval component, and the difference was correlated with the extent to which baseline response rates were higher in the ratio component. In Experiment 2, pigeons were trained on multiple variable-ratio variable-interval schedules in one half of each session and on concurrent chains in the other half in which the terminal links corresponded to the multiple-schedule components. The schedules were varied over six conditions, including two with equated reinforcer rates. In concurrent chains, preference strongly overmatched the ratio of obtained reinforcer rates. In multiple schedules, relative resistance to response-independent food during intercomponent intervals, extinction, and intercomponent food plus extinction depended on the ratio of obtained reinforcer rates but was less sensitive than was preference. When reinforcer rates were similar, both preference and relative resistance were greater for the variable-interval schedule, and the differences were correlated with the extent to which baseline response rates were higher on the variable-ratio schedule, confirming the results of Experiment 1. These results demonstrate that resistance to change and preference depend in part on response rate as well as obtained reinforcer rate, and challenge the independence of resistance to change and preference with respect to response rate proposed by behavioral momentum theory.     

Bias and sensitivity to reinforcement in a concurrent-chain schedule

Six pigeons were trained on concurrent-chain schedules in which the initial links were either dependent (Experiment 1) or independent (Experiment 2) concurrent variable-interval schedules and the terminal links were fixed-duration delays to reinforcement in blackout. A changeover delay of three seconds operated in the initial links. Both the initial- and terminal-link schedule values were varied over 61 experimental conditions. An analysis of the data using the generalized matching law showed that the sensitivity of initial-link response allocation to the frequency of terminal-link production was independent of both the duration of the terminal-link delays and, though less clearly, of the duration of the initial-link schedules. Sensitivity of initial-link response allocation to terminal-link reinforcer-rate ratios was a joint function of the terminal-link durations and the smaller average initial-link duration. The results showed that the generalized matching law is useful in analyzing concurrent-chain schedule performance and that a changeover delay in the initial links eliminates some terminal- to initial-link interactions that have made quantitative predictions for concurrent-chain performances difficult.     

A pharmacological examination of the resistance-to-change hypothesis of response strength.

The effects of d-amphetamine sulfate, sodium pentobarbital, haloperidol, and cholecystokinin-octapeptide were examined within the context of Nevin's (1974, 1979) resistance-to-change hypothesis of response strength. In three experiments, rats' responding was reinforced by delivery of food under chained random-interval 30-s random-interval 30-s, multiple fixed-interval 30-s fixed-interval 120-s, or multiple random-interval 30-s random-interval 120-s schedules. Each rat received several doses of each drug and changes in response rate were measured. The resistance-to-change hypothesis predicts greater disruption of response rate relative to baseline in the initial component of the chained schedule and in the 120-s component of the multiple schedules. In the chained schedule cholecystokinin-octapeptide produced greater reductions in response rate relative to baseline in the initial component. However, no differences between components were observed with haloperidol or sodium pentobarbital, and high doses of d-amphetamine reduced response rate in the terminal component relatively more than in the initial component. In the multiple schedules either no differences were observed between components or response rate was reduced more relative to baseline in the 30-s component. The data fail to support the notion that drugs may be viewed within the same context as other response disruptors such as extinction, satiation, and the presentation of alternative reinforcement.     

Signalled reinforcement and multiple schedules

The responses of four pigeons were first reinforced in the presence of two different wave-lengths (green and red) on a two-ply multiple schedule with identical variable-interval 3-min schedules of reinforcement associated with each component. While the constant-component reinforcement schedule remained unchanged during the experiment, the schedule associated with the variable component was changed to (1) signalled variable time, (2) unsignalled variable time, or (3) signalled variable interval. The probability with which the availability of the reinforcer was signalled in the variable-interval schedules was either 0.5 or 1.0. Positive contrast occurred in both signalled variable-interval and variable-time schedules, but only when the availability of all the variable-component reinforcers was signalled. Signalling the availability of only 50% of the reinforcers in signalled variable-interval schedules resulted in negative induction. The present data suggest that positive behavioral contrast resulting from signalled reinforcer availability is due to the presence of an extinction-correlated stimulus.     

Time and rate measures in choice transitions

Three experiments with pigeons studied the relation between time and rate measures of behavior under conditions of changing preference. Experiment 1 studied a concurrent chain schedule with random-interval initial links and fixed-interval terminal links; Experiment 2 studied a multiple chained random-interval fixed-interval schedule; and Experiment 3 studied simple concurrent random-interval random-interval schedules. In Experiment 1, and to a lesser extent in the other two experiments, session-average initial-link wait-time differences were linearly related to session-average response-rate differences. In Experiment 1, and to a lesser extent in Experiment 3, ratios of session-average initial-link wait times and response rates were related by a power function. The weaker relations between wait and response measures in Experiment 2 appear to be due to the absence of competition between responses. In Experiments 1 and 2, initial-link changes lagged behind terminal-link changes. These findings may have implications for the relations between fixed- and variable-interval procedures and suggest that more attention should be paid to temporal measures in studies of free-operant choice.     

Behavioral contrast: Pavlovian effects and anticipatory contrast.

Two sources of behavioral contrast have been identified previously: Pavlovian stimulus-reinforcer relations and component sequence effects (anticipatory contrast). This study sought to isolate these sources of control procedurally in a four-ply multiple schedule composed of two fixed two-component sequences. Different cues were associated with the first component of each sequence, and contrast effects were studied in these target components. In Experiment 1, differential cuing of Component 2 between sequences and availability of reinforcement during target components were varied across three groups of pigeons; the stimulus-reinforcer relation between target-component cues and schedule of reinforcement in Component 2 was varied within subjects. Control by the Pavlovian relation was demonstrated under all conditions, and anticipatory contrast was not observed. In Experiment 2, target-component duration was systematically varied in the three groups of Experiment 1. Control by the Pavlovian relation was reliably obtained only when target-component behavior was unreinforced, and diminished with increases in component duration. Anticipatory contrast emerged in the two groups for which target-component reinforcement was available. These and other data indicate that Pavlovian effects in multiple schedules may be obscured when the requisite conditions for anticipatory contrast are present.     

Competition between stimulus-reinforcer contingencies and anticipatory contrast.

Procedures used to study anticipatory contrast are conceptually similar to those used to study autoshaping, in that two target stimuli signal either higher or lower rates of reinforcement in the following components of the schedule. Despite this signal contingency, anticipatory contrast entails response rates that are higher to the target stimulus followed by the lower rate of reinforcement. To determine the relation between such effects and autoshaping, different variations of the procedure were used in which the signal contingency was presented in the absence of reinforcement in the target components themselves and in which the reinforcement schedules in the different following components were signaled by the same stimulus. Autoshaping effects of this signal contingency were demonstrated when no reinforcement was available during the target-component signals themselves. Intermediate patterns of behavior occurred when reinforcement was available during the target-component signals and when their different following schedules were correlated with the same stimulus. Attempts to isolate these signal and contrast effects functionally by using the signal-key procedure were unsuccessful. The results demonstrate that Pavlovian stimulus contingencies are in competition with the dynamics of anticipatory contrast, thus reducing its occurrence under some circumstances.     

Absence of anticipatory contrast in rats trained on multiple schedules.

Rats were trained on three- and four-component multiple schedules in which two of the components were correlated with identical reinforcement schedules that remained unchanged throughout training. These target components differed in terms of whether their respective following schedules were either higher or lower in value. Unlike corresponding experiments previously reported with pigeons, higher response rates occurred in the target component followed by a higher valued schedule than in the target component followed by the lower valued schedule. Overall contrast effects occurred independently of these sequential effects, but were inconsistent across subjects. The results suggest that the effects of a following schedule of reinforcement are opposite for pigeons and rats, and that one reason previous studies have often failed to show contrast effects with rats is that the effects of the following schedule in rats are in competition with contrast dynamics.     

Second-order schedules: discrimination of components

Pigeons were exposed to a series of second-order schedules in which the completion of a fixed number of fixed-interval components produced food. In Experiment 1, brief (2 sec) stimulus presentations occurred as each fixed-interval component was completed. During the brief-stimulus presentation terminating the last fixed-interval component, a response was required on a second key, the brief-stimulus key, to produce food. Responses on the brief-stimulus key before the last brief-stimulus presentation had no scheduled consequences, but served as a measure of the extent to which the final component was discriminated from preceding components. Whether there were one, two, four, or eight fixed-interval components, responses on the brief-stimulus key occurred during virtually every brief-stimulus presentation. In Experiment 2, an attempt was made to punish unnecessary responses on the brief-stimulus key, i.e., responses on the brief-stimulus key that occurred before the last component. None of the pigeons learned to withhold these responses, even though they produced a 15-sec timeout and loss of primary reinforcement. In Experiment 3, different key colors were associated with each component of a second-order schedule (a chain schedule). In contrast to Experiment 1, brief-stimulus key responses were confined to the last component. It was concluded that pigeons do not discriminate well between components of second-order schedules unless a unique exteroceptive cue is provided for each component. The relative discriminability of the components may account for the observed differences in initial-component response rates between comparable brief-stimulus, tandem, and chain schedules.     

The following schedule of reinforcement as a fundamental determinant of steady state contrast in multiple schedules

Two experiments investigated whether steady-state interactions in multiple schedules depend exclusively on the following schedule of reinforcement. Experiment 1 used a four-component multiple schedule in which two components were associated with the same constant schedule of reinforcement, and where rate of reinforcement was varied in the component that followed one of these. Contrast effects were reliable only in the component that preceded the point of reinforcement variation, although some contrast did occur otherwise. In those instances where contrast other than the following-schedule effect did occur, it was accounted for by the effect of the preceding schedule, an effect for which there were consistent individual differences among subjects, and which varied with component duration. Experiment 2 used a three-component schedule, in which reinforcement rate was varied in the middle component. The results were consistent with Experiment 1, as the following-schedule effect was the only consistent effect that occurred, although an effect of the preceding schedule did occur for some subjects under some conditions, and was especially evident early in training. The conclusion from both experiments is that there is no general effect of relative rate of reinforcement apart from the sum of the effects of the preceding and following schedules, and that the following-schedule effect is the fundamental cause of steady-state interactions.     

Undermatching and contrast within components of multiple schedules

Six multiple variable-interval schedules each comprised one variable-interval sixty second component and an alternated component which was varied. Four pigeons' responses were recorded in five successive subintervals of each component. Response rate changes across subintervals revealed instances of local contrast and small local induction effects in the changed component. In the constant component, smaller local contrast and larger local induction effects obtained. Accordingly, the magnitude of behavioral contrast, defined as an inverse relation between response rate in the constant component and reinforcement rate in the changed component, did not change reliably across subintervals of the constant component. Ratios of response rates in initial subintervals were highly sensitive to reinforcement ratios. Sensitivity decreased sharply over the first two-fifths of the components and remained constant for the remainder. The results demonstrated that changes in multiple schedule sensitivity are a function of time since the alternation of successive components.