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Reinforcement of inhibition.

A differential-reinforcement-of-other-behavior (DRO) schedule with trials and delayed reinforcement was investigated. Periodically a wheel was briefly available to rats, followed six seconds later by brief availability of a bar. Variable-ratio food reinforcement of wheel turns was adjusted to give 95% turns. After variable-ratio-five reinforcement of bar presses produced 100% pressing, then separate ratio schedules were used for presses following turns (turn presses) and presses following nonturns (nonturn presses). Increasing nonturn-press reinforcements decreased turns, even though total reinforcements increased. Reversal by decreasing nonturn-press reinforcements raised turns, though with hysteresis. Thus food reinforcement increased nonturns even though delayed six to ten seconds after nonturns, a delay that greatly reduces response reinforcement. Those and other results indicate that the turn decrease was not due to reinforcement of competing responses. Evidence against other alternatives, and the reduction of responding by increased reinforcement, indicate that the term inhibition is appropriate for the phenomenon reinforced. Response-specific inhibition appears appropriate for this particular kind, since its effects are more specific to particular responses than Pavlovian conditioned-inhibition. Response-specific inhibition seems best considered a behavioral output comparable to responses (e.g., both reinforcible) but with important properties different from responses (e.g., different reinforcement-delay gradients).

Journal Article↗

The effects of delayed reinforcement on free-operant responding.

In previous studies of delayed reinforcement, response rate has been found to vary inversely with the response-reinforcer interval. However, in all of these studies the independent variable, response-reinforcer time, was confounded with the number of reinforcers presented in a fixed period of time (reinforcer frequency). In the present study, the frequency of available reinforcers was held constant, while temporal separation between response and reinforcer was independently manipulated. A repeating time cycle, T, was divided into two alternating time periods, t(D) and t(Delta). The first response in t(D) was reinforced at the end of the prevailing T cycle and extinction prevailed in t(Delta). Two placements for t(D) were defined, an early t(D) placement in which t(D) precedes t(Delta) and a late t(D) placement in which t(D) follows t(Delta). The duration of the early and late t(D) was systematically decreased from 30 seconds (i.e., t(D) = T) to 0.1 second. Manipulation of t(D) placement and duration controlled the temporal separation between response and reinforcement, but it did not affect the frequency of programmed reinforcers, which was 1/T. The results show that early and late t(D) placements of equal duration have similar overall effects upon response rate, reinforcer frequency, responses per reinforcer, and obtained response-reinforcer temporal separation. A stepwise regression analysis using log response rate as the dependent variable showed that the obtained delay was a significant first-step variable for six of eight subjects, with obtained reinforcer frequency significant for the remaining two subjects.

Journal Article↗

Sensitivity to reinforcer duration in a self-control procedure.

In a concurrent-chains procedure, pigeons' responses on left and right keys were followed by reinforcers of different durations at different delays following the choice responses. Three pairs of reinforcer delays were arranged in each session, and reinforcer durations were varied over conditions. In Experiment 1 reinforcer delays were unequal, and in Experiment 2 reinforcer delays were equal. In Experiment 1 preference reversal was demonstrated in that an immediate short reinforcer was chosen more frequently than a longer reinforcer delayed 6 s from the choice, whereas the longer reinforcer was chosen more frequently when delays to both reinforcers were lengthened. In both experiments, choice responding was more sensitive to variations in reinforcer duration at overall longer reinforcer delays than at overall shorter reinforcer delays, independently of whether fixed-interval or variable-interval schedules were arranged in the choice phase. We concluded that preference reversal results from a change in sensitivity of choice responding to ratios of reinforcer duration as the delays to both reinforcers are lengthened.

Journal Article↗

Determinants of choice for pigeons and humans on concurrent-chains schedules of reinforcement.

Concurrent-chains schedules of reinforcement were arranged for humans and pigeons. Responses of humans were reinforced with tokens exchangeable for money, and key pecks of 4 birds were reinforced with food. Variable-interval 30-s and 40-s schedules operated in the terminal links of the chains. Condition 1 exposed subjects to variable-interval 90-s and variable-interval 30-s initial links, respectively. Conditions 2 and 3 arranged equal initial-link schedules of 40 s or 120 s. Experimental conditions tested the descriptive adequacy of five equations: reinforcement density, delay reduction, modified delay reduction, matching and maximization. Results based on choice proportions and switch rates during the initial links showed that pigeons behaved in accord with delay-reduction models, whereas humans maximized overall rate of reinforcement. As discussed by Logue and associates in self-control research, different types of reinforcement may affect sensitivity to delay differentially. Pigeons' responses were reinforced with food, a reinforcer that is consumable upon presentation. Humans' responses were reinforced with money, a reinforcer exchanged for consumable reinforcers after it was earned. Reinforcers that are immediately consumed may generate high sensitivity to delay and behavior described as delay reduction. Reinforces with longer times to consumption may generate low sensitivity to delay and behavior that maximizes overall payoff.

Animals↗

Effects of central 5-hydroxytryptamine depletion on sensitivity to delayed and probabilistic reinforcement.

RATIONALE: The ascending 5-hydroxytryptaminergic (5-HTergic) pathways are believed to be involved in "impulse control". Rats whose 5-HTergic pathways have been destroyed are more liable than intact rats to select a smaller, immediate reinforcer rather than a larger, delayed reinforcer (impulsive choice), and recent evidence indicates that this effect of central 5-HT depletion reflects a change in the rate of time discounting (i.e. a change in the rate at which reinforcers become devalued as a function of delay). Delay of reinforcement and uncertainty of reinforcer delivery are believed to have equivalent effects on choice behaviour. However, it is not known whether central 5-HT depletion affects choice between probabilistic reinforcers. OBJECTIVE: We examined the effects of central 5-HT depletion on choice behaviour in two experiments: In experiment 1, rats chose between a smaller immediate reinforcer and a larger delayed reinforcer; in experiment 2, rats chose between a smaller certain reinforcer and a larger probabilistic reinforcer. METHODS: Rats received injections of 5,7-dihydroxytryptamine into the dorsal and median raphe nuclei or sham lesions. They were trained to press two levers for food-pellet reinforcers in discrete-trials schedules. In free-choice trials, selection of lever A resulted in immediate delivery of one food pellet; selection of lever B resulted in delivery of 2 pellets, either following a delay (dB) (experiment 1) or with a probability (pB) less than 1 (experiment 2). RESULTS: In experiment 1, both groups showed declining choice of lever B (%B) as a function of dB. The lesioned group showed shorter indifference delays (D50: the value of dB corresponding to %B=50) than the sham-lesioned group. In experiment 2, both groups showed declining choice of lever B as a function of the odds against delivery of the two-pellet reinforcer, thetaB (thetaB=[1/pB]-1). There was no difference between the "indifference odds" (theta50: the value of thetaB corresponding to %B=50) between the two groups. In both experiments, the levels of 5-HT and 5-hydroxyindoleacetic acid were reduced in the brains of the lesioned rats, but the levels of noradrenaline and dopamine were not altered. CONCLUSIONS: These results provide additional evidence that central 5-HTergic mechanisms are involved in time discounting, but provide no evidence for a similar role of 5-HT in rats' sensitivity to probabilistic reinforcement.

Animals↗

Noncontingent delivery of arbitrary reinforcers as treatment for self-injurious behavior.

Results of recent research have shown that noncontingent reinforcement (NCR) can be effective in reducing the frequency of behavior problems. In typical NCR applications, the reinforcer that is responsible for behavioral maintenance (as demonstrated through a functional analysis) no longer follows occurrences of the target behavior but instead is delivered according to a time-based schedule. Thus, it is unclear if NCR would be effective if the target behavior continued to be reinforced or if arbitrary reinforcers (i.e., those irrelevant to behavioral maintenance) were substituted for the maintaining reinforcers in the NCR procedure. In this study, 2 individuals whose self-injurious behavior (SIB) was maintained by positive reinforcement were exposed to conditions in which arbitrary and maintaining reinforcers were withheld and were delivered either contingently or noncontingently. Results indicated that noncontingent delivery of arbitrary reinforcers was effective in reducing SIB even though occurrences of SIB produced access to the maintaining reinforcer. These results suggest that (a) arbitrary reinforcers may sometimes be substituted for maintaining reinforcers, (b) an important component of NCR procedures is alteration of a behavior's establishing operation, and (c) NCR with arbitrary reinforcers might therefore be effective when maintaining reinforcers cannot be identified or withheld during the course of treatment.

Adult↗

Molar versus local reinforcement probability as determinants of stimulus value.

During one component of a multiple schedule, pigeons were trained on a discrete-trial concurrent variable-interval variable-interval schedule in which one alternative had a high scheduled rate of reinforcement and the other a low scheduled rate of reinforcement. When the choice proportion between the alternatives matched their respective relative reinforcement frequencies, the obtained probabilities of reinforcement (reinforcer per peck) were approximately equal. In alternate components of the multiple schedule, a single response alternative was presented with an intermediate scheduled rate of reinforcement. During probe trials, each alternative of the concurrent schedule was paired with the constant alternative. The stimulus correlated with the high reinforcement rate was preferred over that with the intermediate rate, whereas the stimulus correlated with the intermediate rate of reinforcement was preferred over that correlated with the low rate of reinforcement. Preference on probe tests was thus determined by the scheduled rate of reinforcement. Other subjects were presented all three alternatives individually, but with a distribution of trial frequency and reinforcement probability similar to that produced by the choice patterns of the original subjects. Here, preferences on probe tests were determined by the obtained probabilities of reinforcement. Comparison of the two sets of results indicates that the availability of a choice alternative, even when not responded to, affects the preference for that alternative. The results imply that models of choice that invoke only obtained probability of reinforcement as the controlling variable (e.g., melioration) are inadequate.

Animals↗

Concurrent schedules: short- and long-term effects of reinforcers.

Five pigeons were trained on concurrent variable-interval schedules in a switching-key procedure. The overall rate of reinforcement was constant in all conditions, and the ratios of reinforcers obtainable on the two alternatives were varied over seven levels. Each condition remained in effect for 65 sessions, and the last 50 sessions of data from each condition were analyzed. The most recently obtained reinforcer had the largest effect on current preference, but each of the eight previously obtained reinforcers had a small measurable effect. These effects were larger when the reinforcer ratio was more extreme. A longer term effect of reinforcement was also evident, which changed as a function of the reinforcer ratio arranged. More local analyses showed regularities at a reinforcer-by-reinforcer level and large transient movements in preference toward the just-reinforced alternative immediately following reinforcers, followed by a return to stable levels that were related to the reinforcer ratio in effect. The present data suggest that the variables that control choice have both short- and long-term effects and that the short-term effects increased when the reinforcer ratios arranged were more extreme.

Animals↗

Local preference in concurrent schedules: the effects of reinforcer sequences.

We investigated the effects that sequences of reinforcers obtained from the same response key have on local preference in concurrent variable-interval schedules with pigeons as subjects. With an overall reinforcer rate of one every 27 s, on average, reinforcers were scheduled dependently, and the probability that a reinforcer would be arranged on the same alternative as the previous reinforcer was manipulated. Throughout the experiment, the overall reinforcer ratio was 1:1, but across conditions we varied the average lengths of same-key reinforcer sequences by varying this conditional probability from 0 to 1. Thus, in some conditions, reinforcer locations changed frequently, whereas in others there tended to be very long sequences of same-key reinforcers. Although there was a general tendency to stay at the just-reinforced alternative, this tendency was considerably decreased in conditions where same-key reinforcer sequences were short. Some effects of reinforcers are at least partly to be accounted for by their signaling subsequent reinforcer locations.

Animals↗

Independent ethanol- and sucrose-maintained responding on a multiple schedule of reinforcement.

Assessment of drug effects on two different reinforcers at the same time requires that each reinforcer be sampled at approximately the same time. One procedure that effectively produces this result is the use of a multiple schedule of reinforcement in which two different reinforcers are presented in alternating 2-min components. In our study, sucrose and ethanol solutions were made available after appropriate lever-press responding. Subjects were trained to self-administer 10% ethanol using a sucrose-substitution procedure and to discriminate light cues associated with the different reinforcers until stable reinforcer-directed responding was achieved on both the ethanol- and the sucrose-associated lever during the changing 2-min components of the schedule. Subsequently, the reinforcer solution presented on one lever was held constant while the concentration of the alternate reinforcer was manipulated, i.e., ethanol concentrations of 0 to 15% and sucrose concentrations of 0 to 10% were assessed. This multiple schedule procedure resulted in sustained and independent ethanol- and sucrose-reinforced behavior. Manipulation of the characteristics of one reinforcer had no effect on behavior maintained by the alternate reinforcer. Increases in sucrose concentration resulted in increases in sucrose-directed responding with no change in ethanol responding, and increases in ethanol concentration resulted in increases in ethanol intake with no change in sucrose responding. Our methods can be used to examine differential drug effects on ethanol- and sucrose-reinforced behavior in the same animal over a single time course without the confounds or interference from the concurrently available reinforcer.

Animals↗

Concurrent performances: inhibition of one response by reinforcement of another.

In an analysis of interactions between concurrent performances, variable-interval reinforcement was scheduled, in various sequences, for both keys, for only one key, or for neither key of a two-key pigeon chamber. With changeover delays of 0.5 or 1.0 sec, and with each key's reinforcements discriminated on the basis of key-correlated feeder stimuli, reinforcement of pecks on one key reduced the pecking maintained by reinforcement on the other key. The decrease in pecking early after reinforcement was discontinued on one key was not substantially affected by whether pecks on the other key were reinforced, but after reinforcement was discontinued on both keys, reinstatement of reinforcement for one key sometimes produced transient increases in pecking on the other key. Correlating the availability of right-key reinforcements with a stimulus, which maintained right-key reinforcement while reducing right-key pecking to negligible levels, demonstrated that these interactions depended on concurrent reinforcement, not concurrent responding. Thus, reinforcement of a response, but not necessarily the occurrence of the response, inhibits other reinforced responses. Compared with accounts in terms of excitatory effects of extinction, often invoked in treatments of behavioral contrast, this inhibitory account has the advantage of dealing only with observed dimensions of behavior.

Journal Article↗

Effects of rate of reinforcement-time upon concurrent operant performance.

Three experiments were conducted to investigate the theoretical reduction of rate and duration of reinforcement to their product, rate of reinforcement-time, under concurrent chain schedules. In Exp. I, rate of reinforcement-time was varied by varying rate of reinforcement delivery, holding duration of reinforcement availability constant; in Exp. II, rate of reinforcement-time was varied by holding rate of reinforcement delivery constant and varying duration of reinforcement availability; in Exp. III, rate of reinforcement-time was held constant by varying both rate and duration of reinforcement simultaneously and inversely. For all three experiments, both relative rate of responding and relative time spent in the initial link were found to match approximately the relative rate of reinforcement-time arranged in the terminal link. These data were interpreted as support for the notion that rate and duration of reinforcement may be functionally equivalent and reducible to a single variable, rate of reinforcement-time.

Journal Article↗

Two-key concurrent paced variable-interval paced variable-interval schedules of reinforcement.

Nine pigeons were used in two experiments in which a response was reinforced if a variable-interval schedule had assigned a reinforcement and if the response terminated an interresponse time within a certain interval, or class, of interresponse times. One such class was scheduled on one key, and a second class was scheduled on a second key. The procedure was, therefore, a two-key concurrent paced variable-interval paced variable-interval schedule. In Exp. I, the lengths of the two reinforced interresponse times were varied. The relative frequency of responding on a key approximately equalled the relative reciprocal of the length of the interresponse time reinforced on that key. In Exp. II, the relative frequency and relative magnitude of reinforcement were varied. The relative frequency of responding on the key for which the shorter interresponse time was reinforced was a monotonically increasing, negatively accelerated function of the relative frequency of reinforcement on that key. The relative frequency of responding depended on the relative magnitude of reinforcement in approximately the same way as it depended on the relative frequency of reinforcement. The relative frequency of responding on the key for which the shorter interresponse time was reinforced depended on the lengths of the two reinforced interresponse times and on the relative frequency and relative magnitude of reinforcement in the same way as the relative frequency of the shorter interresponse time depended on these variables in previous one-key concurrent schedules of reinforcement for two interresponse times.

Journal Article↗

Fixed-ratio pausing: Joint effects of past reinforcer magnitude and stimuli correlated with upcoming magnitude.

Pigeons responded on fixed-ratio schedules ending in small or large reinforcers (grain presentations of different duration) interspersed within each session. In mixed-schedule conditions, the response key was lit with a single color throughout the session, and pausing was directly related to the past reinforcer (longer pauses after large reinforcers than after small ones). In multiple-schedule conditions, different colors accompanied the ratios ending in small and large reinforcers, and pausing was affected by the upcoming reinforcer as well as the past one. Pauses were shorter before large reinforcers than before small ones, but they continued to be longer after large reinforcers than after small ones. The influence of the past reinforcer was modulated by the magnitude of the upcoming reinforcer; in the presence of the stimulus before the small reinforcer, the effect of the past reinforcer was enhanced relative to its effect in the stimulus before the large reinforcer. These results show that pausing between ratios is jointly determined by two competing factors: past conditions of reinforcement and stimuli correlated with upcoming conditions.

Journal Article↗

Contrast and reallocation of extraneous reinforcers between multiple-schedule components.

Four pigeons responded in components of multiple schedules in which two responses were available and reinforced with food. Pecks on the left key ("main" key) were reinforced at a constant rate in one component and at a rate that varied over conditions in the other component. When reinforcer rate was varied, behavioral contrast occurred in the constant component. On the right key ("extra" key), five variable-interval schedules and one variable-ratio schedule, presented conjointly, arranged reinforcers for responses in all conditions. These conjoint schedules were common to both multiple-schedule components-rather than unique to particular components-and reinforcers from these schedules could therefore be arranged in one component and obtained during the other component. In this way, the additional reinforcers were analogous to the "extraneous" reinforcers thought to maintain behavior other than pecking in conventional multiple schedules. Response rate on the extra key did not change systematically over conditions in the constant component, and in the varied component extra responding was inversely related to main-key reinforcement. All subjects obtained more extra-key reinforcers in whichever component arranged fewer main-key reinforcers. Consistent with the theory that reallocation of extraneous reinforcers may cause behavioral contrast, absolute reinforcer rate for the extra key in the constant component was low in conditions that produced positive contrast on the main key and high in those that produced negative contrast. Also consistent with this theory, behavioral contrast was reduced in two conditions that canceled extra-key reinforcers that had been arranged but not obtained at the end of components. Thus, a constraint on reallocation markedly reduced the extent of contrast.

Journal Article↗

Clinical survey of acrylic resin removable denture repairs with glass-fiber reinforcement.

PURPOSE: The aim of this study was to evaluate clinical usefulness and durability of continuous glass-fiber reinforcement in repair of acrylic resin removable dentures. MATERIALS AND METHODS: Fractured removable dentures without reinforcement, with conventional metal-wire reinforcement, or with mesh reinforcement were collected from two dental schools in Finland. The total number of dentures was 51 and the number of patients was 48. During the repair, the dentures were reinforced with a polymer-preimpregnated E-glass fiber at the region of the fracture. The fibers were used as partial fiber reinforcement, i.e., only the weakest part of the denture was reinforced. Follow-up time varied from 4 months to 4.1 years. After the follow-up period, possible fractures and discoloring were visually inspected. Possible irritation of oral mucosa by glass fibers and the general shape of the denture were also evaluated. RESULTS: In 88% of the cases, there was no need for adjustment at the region of partial fiber reinforcement, and the clinical condition of the dentures was good. Glass fibers did not irritate the oral mucosa. In the case of refracture or hairline fracture, positioning of the partial fiber reinforcement was incorrect or the reinforcement had been used incorrectly (the wetting of the reinforcement with denture base resin was inadequate). CONCLUSION: Polymer-preimpregnated partial fiber reinforcement seems to be useful in eliminating fractures of acrylic resin removable dentures. However, this study emphasizes the importance of correct positioning and accurate laboratory technique when partial fiber reinforcement is used.

Acrylic Resins↗

Effects of adding a second reinforcement alternative: implications for Herrnstein's interpretation of r(e).

Herrnstein's hyperbola describes the relation between response rate and reinforcer rate on variable-interval (VI) schedules. According to Herrnstein's (1970) interpretation, the parameter r(e) represents the reinforcer rate extraneous to the alternative to which the equation is fitted (the target alternative). The hyperbola is based on an assumption that extraneous reinforcer rate remains constant with changes in reinforcer rate on the target alternative (the constant-r(e) assumption) and that matching with no bias and perfect sensitivity occurs between response and reinforcer ratios. In the present experiment, 12 rats pressed levers for food on a series of 10 VI schedules arranged on the target alternative. Across conditions, six VI values and extinction were arranged on a second alternative. Reinforcer rate on the second alternative, r2, negatively covaried with reinforcer rate on the target alternative for five of the six VI values on the second alternative, and significant degrees of bias and undermatching occurred in response ratios. Given covariation of reinforcer rate on the second and target alternatives, the constant-r(e) assumption can be maintained only by assuming that reinforcer rate from unmeasured background sources, rb, covaries with reinforcer rate on the second alternative such that their sum, r(e), remains constant. In a single-schedule arrangement, however, r(e) equals rb and thus rb is assumed to remain constant, forcing a conceptual inconsistency between single- and concurrent-schedule arrangements. Furthermore, although an alternative formulation of the hyperbola can account for variations in bias and sensitivity, the modified equation also is based on the constant-r(e) assumption and therefore suffers from the same logical problem as the hyperbola when reinforcer rate on the second alternative covaries with reinforcer rate on the target alternative.

Animals↗

Relationship of reinforcement by student clinicians and peers to accuracy of imitated grammatical constructions during language training.

Percentages of correctly imitated grammatical constructions were examined within a framework of reinforcement theory. Four small treatment groups, each of 4 language-delayed children, were repeatedly observed interacting with different student-clinicians. The Therapy Reinforcement Schedule was used to obtain frequency counts of verbal and non-verbal reinforcements so that within each language group the students could be objectively divided into those who frequently and infrequently were reinforcing, and the children into those for whom peer-reinforcement was high or low. The resulting 4 groups were compared for proportions of accurately imitated constructions with a repeated-measures analysis of variance design (student-clinicians' reinforcement x peers' reinforcement x trials). Correctly scored imitations increased significantly over trials. In addition, children interacting with frequently reinforcing students received higher imitation scores than those with infrequently rewarding ones. Significant main effects of reinforcement by the peer group were not observed, although a reliable interaction of student-clinicians' reinforcement x peers' reinforcement was present. Regression analyses indicated the importance of certain types of reinforcements in predicting accuracy of imitation.

Child, Preschool↗