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The effects of magnitude and quality of reinforcement on choice responding during play activities.

Three boys with autism participated in a study of the effects of magnitude and quality of reinforcement on choice responding. Two concurrent response alternatives were arranged: (a) to play in an area where a peer or sibling was located, or (b) to play in an area where there was no peer or sibling. During one condition, the magnitude (i.e., duration of access to toys) or quality (level of preference) of reinforcement provided for both responses was equal. During the other condition, the magnitude or quality of reinforcement was relatively greater for choosing the play area where the peer or sibling was located than the area where the peer or sibling was not located. Results showed that after repeated exposure to the unequal magnitude or quality condition, the participant increasingly allocated his responses to the play area where the peer or sibling was located. For 2 participants, this pattern of responding was maintained in the subsequent equal magnitude or quality condition. Overall, the analysis suggests that the dimensions of magnitude and quality of reinforcement can be arranged to influence choice responding in favor of playing near a peer or sibling rather than playing alone.

Attention↗

Treatment efficacy of noncontingent reinforcement during brief and extended application.

We evaluated the long-term therapeutic effects of noncontingent reinforcement (NCR). In Experiment 1, NCR effects were examined with 2 participants' arbitrary responses; in Experiment 2, NCR was used as treatment with 3 participants whose self-injurious behavior (SIB) was maintained by automatic reinforcement. In both experiments, NCR consisted of continuous access to a highly preferred leisure item and was implemented initially during 10-min and later during 120-min sessions. Varied reinforcers (leisure items) were subsequently introduced during 120-min sessions to determine if treatment effects might be extended. Finally (Experiment 2 only), NCR was implemented throughout the day in participants' homes. Results of Experiments 1 and 2 showed that reinforcers obtained through object manipulation can compete with those obtained automatically by engaging in SIB during brief NCR sessions. However, data from the 120-min sessions indicated that satiation to a specific leisure item might occur over periods of time more typical of those during which treatment would be implemented. Access to a variety of highly preferred leisure items extended the effectiveness of NCR for some individuals. When NCR was implemented throughout the day (Experiment 2), therapeutic effects were shown to be maintained for up to 1 year.

Adult↗

Persistence of stereotypic behavior: examining the effects of external reinforcers.

Basic research has shown that behavioral persistence is often positively related to rate of reinforcement. This relation, expressed in the metaphor of behavioral momentum, has potentially important implications for clinical application. The current study examined one prediction of the momentum metaphor for automatically reinforced behavior. Participants were 3 children who had been diagnosed with an autism spectrum disorder and who engaged in stereotypic behavior maintained by automatic reinforcement. Results suggested that stereotypic behavior was more resistant to disruption following periods of access to preferred stimuli delivered on a variable-time schedule than following periods without access to preferred stimuli. The implications of these findings for the treatment of automatically reinforced behavior are discussed.

Attention↗

Effects of stimulus variation on the reinforcing capability of nonpreferred stimuli.

We examined the effects of stimulus (reinforcer) variation in several different contexts. In Study 1, we identified high-quality (HQ) and low-quality (LQ) stimuli based on results of a paired-stimulus assessment and examined their effects when available under concurrent-reinforcement schedules for 8 participants. No participants showed preference for the LQ stimuli when compared singly or in a varied arrangement to the HQ stimulus. In Study 2, we identified nonpreferred (NP) stimuli based on results of a single-stimulus assessment and examined their effects when available under single-reinforcement schedules for 3 participants. Results of Study 2 were mixed. One participant's data indicated that the varied presentation of NP stimuli produced a modest improvement in performance over that observed when the stimuli were presented singly. By contrast, a second participant's data showed no facilitative effect for the varied delivery of NP stimuli and that the inclusion of an HQ stimulus in the varied arrangement obscured the reinforcing effects of the HQ stimulus. The 3rd participant's data showed no effect for the varied delivery of NP stimuli but an apparent facilitative effect when an HQ stimulus was included in the varied arrangement, which was attributable solely to the presence of the HQ stimulus.

Adult↗

Independence of concurrent responding maintained by interval schedules of reinforcement.

A pigeon's responses were reinforced on a variable-interval schedule on one key; and, concurrently, either a multiple or a fixed-interval schedule of reinforcement was in effect on a second key. These concurrent schedules, conc VI 3 (mult VI 3 EXT) or conc VI 3 FI 6, were programmed with or without a changeover delay (COD). Because the COD provided that responses on one key could not be followed by reinforced responses on the other key, responding on one key was not likely to accidentally come under the control of the reinforcement schedule on the other. When the COD was used, the performances on each key were comparable to the performances maintained when these interval schedules are programmed separately. The VI schedule maintained a relatively constant rate of responding, even though the rate of responding on the second key varied in a manner appropriate to the schedule on the second key. The mult VI 3 EXT schedule maintained two separate rates of responding: a relatively high rate during the VI 3 component, and almost no responding during the EXT component. The FI schedule maintained the gradually increasing rate of responding within each interval that is characteristic of the performance maintained by this schedule. The concurrent performances, however, did include certain interactions involving the local characteristics of responding and the over-all rates of responding maintained by the various schedules. The relevance of the present findings to an inter-response time analysis of VI responding, a chaining account of FI responding, and the concept of the reflex reserve was discussed.

Animals↗

RELATIVE RATE OF RESPONSE AND RELATIVE MAGNITUDE OF REINFORCEMENT IN MULTIPLE SCHEDULES.

Pigeons were trained on a multiple schedule in which the duration of access to grain reinforcement was varied independently in the two components. The relative response rate in one component was an increasing function of the relative duration of reinforcement in that component. The similarity of this interaction to that found in multiple schedules of different reinforcement frequency is discussed. Extinction data were also similar to those obtained after training on multiple schedules of different reinforcement frequency.

Animals↗

VARIABLES DETERMINING THE EFFECTS OF DELAY IN REINFORCEMENT.

Procedures were discovered for maintaining a small fixed-ratio performance under 24-hr delay in reinforcement, by appropriate manipulation of the length of delay, amount of food delivered, and size of the fixed ratio. Other experiments showed that (1) the parameters discovered in the first experiment could produce the same result without the complex history of the first procedures; (2) the same parameters of the delayed-reinforcement procedure could maintain an explicit chain of responses; (3) gradual increase in the delay in reinforcement from small to large values was not a necessary condition for achieving the major result, if large amounts of food were delivered as reinforcement and all of the behaviors were first under good control of the relevant stimuli with short delays.

Animals↗

DISCRIMINATIVE FUNCTIONS BASED ON A DELAY IN THE REINFORCEMENT RELATION.

Pigeons were shown to come under discrimination control when the S(D) and S(Delta) were temporally separated from reinforcement and non-reinforcement. S(D) and S(Delta) consisted of distinctive key illuminations presented separately. Responding on an FR 5 in the presence of S(D) or S(Delta) produced a third stimulus containing a schedule requirement. If this third (or interpolated) stimulus was preceded by S(D), responding in its presence produced reinforcement followed by a time-out (TO). If, on the other hand, the third stimulus was preceded by S(Delta), responding produced TO alone. In this fashion, the same stimulus and the same response requirement were imposed between S(D) and the reinforcement as between S(Delta) and the TO. In Experiment I, the schedule employed during the interpolated stimulus was FR; in Experiment II, FI. Discrimination reversal was accomplished in both experiments.

Animals↗

Human, free-operant avoidance of "time out" from monetary reinforcement.

To assess the aversive effects of withdrawing monetary reinforcement, human subjects were exposed to a free-operant avoidance procedure in which periods of no reinforcement occurred if the subject failed to respond, and each response postponed withdrawal of reinforcement. Avoidance behavior was developed either through specific instructions about the consequence of responding or through preliminary escape-avoidance training. In all cases, rates of response were found to be a positively accelerated function of decreases in the duration by which responding postponed reinforcement withdrawal. The findings with respect to the function relating avoidance behavior to the interval of postponement were viewed as similar to those obtained when shock is used as the aversive event in free-operant avoidance conditioning.

Avoidance Learning↗

The reinforcement of least-frequent interresponse times.

A new schedule of reinforcement was used to maintain key-pecking by pigeons. The schedule reinforced only pecks terminating interresponse times which occurred least often relative to the exponential distribution of interresponse times to be expected from an ideal random generator. Two schedule parameters were varied: (1) the rate constant of the controlling exponential distribution and (2) the probability that a response would be reinforced, given that it met the interresponse-time contingency. Response rate changed quickly and markedly with changes in the rate constant; it changed only slightly with a fourfold change in the reinforcement probability. The schedule produced stable rates and high intra- and inter-subject reliability, yet interresponse time distributions were approximately exponential. Such local interresponse time variability in the context of good overall control suggests that the schedule may be used to generate stable, predictable, yet sensitive baseline rates. Implications for the measurement of rate are discussed.

Animals↗

On the measurement of reinforcement frequency in the study of preference.

In a two-link, concurrent-chain schedule, pigeons' pecks on each key during the initial link occasionally produced a terminal link, during which only that key was operative. Responses in the terminal link were reinforced with food on either fixed-interval or variable-interval schedules. In one experiment, relative amount of responding in the initial link equaled the relative harmonic rate of reinforcement in the terminal links. In a second experiment, the selection of interreinforcement intervals in variable-interval schedules in the terminal links was such that rates of reinforcement based on the harmonic or on the arithmetic means of the interreinforcement intervals predicted opposite preferences in the initial links. The observed preference was consistent with that predicted by the harmonic rather than by the arithmetic rates of reinforcement.

Animals↗

Punishment and rate of positive reinforcement.

This experiment investigated the effect of several punishment intensities on two responses maintained by contrasting rates of reinforcement. The responses were concurrently reinforced according to two different variable-interval schedules. Because these schedules were independent of one another and programmed different rates of reinforcement, the two responses occurred at dissimilar rates. When responses were simultaneously suppressed by punishment, both rates were reduced proportionately until suppression was virtually complete. In other words, the per cent suppression resulting from punishment was independent of the rate at which the response was reinforced. Phenomena found in single-response studies were duplicated here. Responding tended to increase both within and between punishment sessions at mild and moderate punishment intensities. Cessation of punishment led to a "compensatory" overshooting beyond the prepunished response rate.

Animals↗

Use of progressive fixed-ratio procedures in the assessment of intracranial reinforcement.

Six rats with electrodes chronically implanted in septal or hypothalamic sites were tested for intracranial reinforcement on a progressive fixed-ratio schedule. Two variations of this schedule were also examined and compared. Functions relating the highest level of stable fixed-ratio responding to a wide range of stimulus currents were, unlike those derived from continuous reinforcement rates, monotonic at all stimulation sites tested. One of the procedures described, in particular, is quite sensitive to intracranial reinforcement parameters, provides a reliable technique for within-session assays of these parameters, and successfully avoids many problems commonly encountered with administration of central stimulation on a continuous reinforcement schedule.

Animals↗

Actual versus potential shock in making shock situations function as negative reinforcers.

The relative importance of potential and actual shocks in making shock situations function as negative reinforcers was studied. Shocks were scheduled to occur at the same rate during two stimuli. During one, squirrel monkeys could avoid the shocks; during the other, they were unavoidable. For the two stimuli the potential rate of shocks was the same, but the actual rate was lower during avoidance because of avoidance responding. Fixed-ratio responding was maintained by the change from unavoidable shock to avoidance, indicating that the change was reinforcing when it resulted in a reduction in actual shock rate with no reduction in potential shock rate. Further increases in the rate of potential shock during avoidance had little effect upon the fixed-ratio responding until the rate was increased to the point that the actual shock rate during avoidance was comparable with that during unavoidable shock. At that point, the fixed-ratio response rate decreased nearly to zero. These findings show that actual shocks are more important than potential shocks in determining whether or not a shock situation will function as a negative reinforcer; this explains why the change from unavoidable shock to avoidable shock is reinforcing.

Animals↗

Discriminative responding on associated mixed and multiple schedules as a function of food and ICS reinforcement.

Performance on associated mixed and multiple variable-interval-extinction schedules was studied as a function of food versus intracranial stimulation (ICS) reinforcement. For the mixed schedule, differential responding was greater for an ICS reinforcement group than for a food reinforcement group, demonstrating that conditions affecting resistance to extinction help to determine the control exerted by a mixed schedule. Performance on the multiple schedule demonstrated greater differential responding for an ICS group than for a food reinforcement group during the early training sessions, indicating that the control exerted by mixed schedules interacts with that exerted by the exteroceptive discriminative stimuli. The results suggest that the influence of the associated mixed schedule on discriminative responding would be greater, the greater the difficulty of the stimulus discrimination.

Animals↗

Choice, foraging, and reinforcer duration.

Pigeons were exposed to a foraging schedule characterized by three different states, beginning with a search state in which completion of a variable interval on a white key led to a choice state. In the choice state the subject could, by appropriate responding on a fixed ratio of three, either accept or reject the schedule offered. If the subject accepted the schedule, it entered a handling state in which the appropriate reinforcer amount was presented according to a variable-interval schedule. In Experiment 1 the shorter duration reinforcer was more likely to be accepted the longer the duration of the search state and the shorter the equal durations of the handling states. In Experiment 2 the shorter duration reinforcer was more likely to be accepted the longer the handling time preceding the longer duration reinforcer. All of the results were in qualitative--and some were in quantitative--agreement with those predicted by the delay-reduction hypothesis and the optimal-diet model.

Animals↗

Bouts of responding from variable-interval reinforcement of lever pressing by rats.

Four rats obtained food pellets by lever pressing. A variable-interval reinforcement schedule assigned reinforcers on average every 2 min during one block of 20 sessions and on average every 8 min during another block. Also, at each variable-interval duration, a block of sessions was conducted with a schedule that imposed a variable-ratio 4 response requirement after each variable interval (i.e., a tandem variable-time variable-ratio 4 schedule). The total rate of lever pressing increased as a function of the rate of reinforcement and as a result of imposing the variable-ratio requirement. Analysis of log survivor plots of interresponse times indicated that lever pressing occurred in bouts that were separated by pauses. Increasing the rate of reinforcement increased total response rate by increasing the rate of initiating bouts and, less reliably, by lengthening bouts. Imposing the variable-ratio component increased response rate mainly by lengthening bouts. This pattern of results is similar to that reported previously with key poking as the response. Also, response rates within bouts were relatively insensitive to either variable.

Animals↗

Is induction produced by upcoming food-pellet reinforcement the outcome of an increase in overall activity or in operant responding?

Researchers have demonstrated that rats reliably increase their rates of pressing a lever for 1% liquid-sucrose reinforcement if they will soon have the opportunity to press a lever for food-pellet reinforcement. In the present experiments, the authors investigated if this increase in response rates occurred because the upcoming food pellets produced an increase in all behaviors (i.e., general arousal) or an increase in only the specific operant response (i.e., lever pressing). The results of Experiments 1 and 2 showed that the appearance of induction in rats' lever pressing for 1% sucrose reinforcement when food-pellet reinforcement was upcoming did not coincide with increases in the frequency of running in a wheel or making a nonreinforced nose-poke response. On the other hand, in Experiment 3, the authors found the appearance of induction coincided with increase nonreinforced lever presses on an adjacent lever. These results shed doubt on the idea that induction is a result of a general increase in all activity, and suggest instead that the increase in responding that occurs during induction is limited to the operant response.

Animals↗