The effects of differential and lag reinforcement schedules on varied verbal responding by individuals with autism

Variability has been shown to be a reinforceable dimension of behavior. One procedure that has been demonstrated to increase variability in basic research is the lag reinforcement schedule. On this type of schedule, a response is reinforced if it differs from a specified number of previous responses. Lag schedules are rarely used, however, for increasing response variability in applied settings. The purpose of the present study was to investigate the effects of a lag schedule of differential reinforcement on varied and appropriate verbal responding to social questions by 3 males with autism. A reversal design with a multiple baseline across subjects was used to evaluate the effects of the lag schedule. During baseline, differential reinforcement of appropriate responding (DRA) resulted in little or no varied responding. During the intervention, a Lag 1 requirement was added to the DRA (Lag 1/DRA) resulting in an increase in the percentage of trials with varied and appropriate verbal responding for 2 of the 3 participants. In addition, an increase in the cumulative number of novel verbal responses was also observed for the same 2 participants. These results are discussed in terms of reinforcement schedules that support variability, generalization, and potential stimulus control over varied responding.     

Matching, contrast, and equalizing in the concurrent lever-press responding of rats

Five rats pressed levers for food reinforces delivered by several concurrent variable-interval variable-interval schedules. The rate of reinforcement available for responding on one component schedule was held constant at 60 reinforcers per hour. The rate of reinforcement available for responding on the other schedule varied from 30 to 240 reinforcers per hour. The behavior of the rats resembled the behavior of pigeons pecking keys for food reinforcers. The ratio of the overall rates of responding emitted under, and the ratio of the time spent responding under, the two components of each concurrent schedule were approximately equal to the ratio of the overall rates of reinforcement obtained from the components. The overall rate of responding emitted under, and the time spent responding under, the variable component schedule varied directly with the overall rate of reinforcement from that schedule. The overall rate of responding emitted under, and the time spent responding under, the constant component schedule varied inversely with the overall rate of reinforcement obtained from the variable component. The local rates of responding emitted under, and the local rates of reinforcement obtained from, the two components did not differ consistently across subjects. But they were not exactly equal either.     

Positive interaction (induction) in multiple variable-interval, differential-reinforcement-of-high-rate schedules

The effect of increases in the rate of responding in one component of a multiple schedule upon the rate of responding in a second component was investigated. Pigeons were exposed to a multiple schedule where both components were initially variable-interval schedules having the same parameter value. After rate of key pecking stabilized, one component was changed to a schedule that differentially reinforced high rates of responding. Rate of reinforcement in this varied component was adjusted to remain equal to rate of reinforcement in the constant (variable-interval) component. Four of five pigeons showed a maintained increase in rate of responding during both the constant and varied components, even though rates of reinforcement did not change.     

Evaluating skills correlated with discriminated responding in multiple schedule arrangements

One potential solution for excessively high‐rate functional communication responses (FCR) is to establish stimulus control of the FCR through a multiple schedule. However, several studies have demonstrated difficulty with establishing discriminated responding across multiple schedule components. The primary aim of the current study was to evaluate how participants’ skills related to color discrimination may be related to the emergence of discriminated responding in a multiple schedule with colors as the schedule‐correlated stimuli. Three secondary aims of the current study were to evaluate: a) varied multiple schedule arrangements, b) if topographically dissimilar stimuli facilitated the emergence of discriminated responding, and c) if employing different colored stimuli across multiple schedule arrangements reduced the likelihood that discriminated responding emerged simultaneously across varied arrangements. Nine participants’ ability to match, select, tact, and respond intraverbally to colors was assessed, and 1 of 2 evaluations of multiple schedule arrangements were conducted. Results indicated that participants’ ability to select and tact colors was strongly correlated with the efficacy of standard multiple schedule arrangements. Additionally, multiple schedule arrangements employing topographically dissimilar stimuli were observed to be equally as effective as standard arrangements and the inclusion of different colored stimuli across arrangements did not reduce the likelihood that discriminated responding emerged simultaneously across all conditions, when it was observed to emerge at all.     

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.     

Schedule-induced mirror responding in the pigeon

Two pigeons that were previously exposed to a multiple schedule of reinforcement in the presence of a stuffed and a live pigeon, and two of three naive pigeons, responded on a mirror during exposure to multiple fixed-ratio, fixed-ratio schedules of reinforcement for key pecking. Both the topography and temporal pattern of mirror responding were comparable to schedule-induced “attack” on live and stuffed targets. Rate of target responding was reduced when either the mirror was covered with paper or when the multiple schedule was removed. A reversal in the relationship between reinforcement schedules and discriminative stimuli demonstrated that mirror responding was controlled by the stimulus correlated with the higher fixed-ratio schedule. With one component of the multiple schedule held constant at fixed ratio 25 and the ratio requirement of the other component varying from 25 to 150, there was an inverted U-shaped relationship between rate of mirror responding and fixed-ratio schedule in the varied component. As in Flory's study (1969b) there was an inverted U-shaped relationship between target responding and inter-food intervals. The combined results of these studies suggest that the relationship between rate of target responding and reinforcement schedules is controlled primarily by the inter-food intervals resulting from the schedules.     

Fixed and variable schedules of response-independent reinforcement

After response-dependent reinforcement established key-pecking as the predominant response, pigeons received schedules in which reinforcements occurred without reference to responding. These response-independent schedules involved either a reinforcement every 5 min, or reinforcements at irregular intervals that averaged 5 min. The response-independent schedules generated characteristic patterns of responding. The fixed schedule produced positively accelerated responding between reinforcements, and the variable schedule produced either steady rates, erratic, or negatively accelerated patterns. The patterns developed independent of the distribution of responses existing when the schedule was first imposed. The rate of responding varied for the three birds, but, for all, response-independent schedules decreased the rates below the level maintained by response-dependent reinforcement. Although the rate of responding was affected primarily by the events contiguous with reinforcement, the pattern of responding appeared to be determined mainly by the presentation of reinforcements in relation to time.     

CHANGES IN BLOOD PRESSURE AND HEART RATE DURING FIXED‐INTERVAL RESPONDING IN SQUIRREL MONKEYS

Episodic and sustained increases in heart rate and mean arterial blood pressure can occur with recurring patterns of schedule‐controlled behavior. Most previous studies were conducted under fixed‐ratio schedules, which maintained a consistent high rate of responding that alternated with periods of no responding during times when the schedule was not in operation. The present study examined changes in heart rate and blood pressure under fixed‐interval schedules which maintained a range of rates that varied from little or no responding at the beginning of the fixed interval to high rates at the end of the interval. The relations of cardiovascular function to rate of responding were examined. Squirrel monkeys prepared with arterial catheters were trained to respond under fixed‐interval schedules of electric‐shock presentation. The duration of the interval was varied across sessions and cardiovascular parameters were examined. Local rates of responding were typically near zero during timeout periods, low at the beginning of each fixed‐interval cycle, and then increased as the fixed interval progressed. At most schedule durations, arterial blood pressure and heart rate levels were lowest at the beginning of the interval cycles, increased as the rate of responding increased, and then decreased during the timeout periods. At all parameters studied, there was a direct relationship between changes in response rate within fixed‐interval cycles and changes in heart rate and blood pressure. The results suggest that a much closer concordance of these cardiovascular parameters and schedule‐controlled responding is obtained by examining ongoing behavior as it occurs within the contingencies by which it is maintained.     

The relative law of effect: effects of shock intensity on response strength in multiple schedules

Key pecking of four birds was reinforced with food according to a two-component multiple variable-interval 1-minute variable-interval 4-minute schedule. In addition, key pecking was punished by a brief shock according to a variable-interval 30-second schedule during both components of the multiple schedule. The intensity of the shock was varied. For all birds, punishment had a stronger suppressive effect on the responding maintained by the leaner food schedule, and the ratio of responding during the two components of the multiple schedule became closer to the ratio of reinforcement as shock intensity was increased, as the relative law of effect predicts. At the higher shock intensity, there was some evidence that the ratio of responses overmatched the ratio of reinforcements.     

Concurrent ratio schedules: Fixed vs. variable response requirements

Rats were trained on concurrent fixed-ratio variable-ratio or concurrent fixed-ratio mixed-ratio schedules of food reinforcement. The variable-ratio schedule was composed of an arithmetic sequence of 11 ratios that averaged 50; the mixed-ratio schedule consisted of equiprobable ratios of 1 and 99. Fixed-ratio values, varied over experimental conditions, included 25, 35, 50, 60, and 99. The proportion of responses and time allocated to the variable- or mixed-ratio schedule increased as the size of the fixed ratio increased. For most subjects, higher proportions of responses and time were maintained on the fixed-ratio schedule at fixed-ratio values of 25 and 35; higher proportions of responses and time were maintained on the variable- or mixed-ratio schedule at fixed-ratio values of 50 or higher. On concurrent variable-ratio fixed-ratio schedules, the tendency for responding to be maintained exclusively by one schedule was related to the difference in local reinforcement rates obtained from those schedules. Exclusive responding was approximated when the difference in local reinforcement rates obtained from those schedules was large; responding was more evenly distributed between the schedules as the difference in the rates at which reinforcement was obtained from each decreased.     

A quantitative analysis of the responding maintained by interval schedules of reinforcement

Interval schedules of reinforcement maintained pigeons' key-pecking in six experiments. Each schedule was specified in terms of mean interval, which determined the maximum rate of reinforcement possible, and distribution of intervals, which ranged from many-valued (variable-interval) to single-valued (fixed-interval). In Exp. 1, the relative durations of a sequence of intervals from an arithmetic progression were held constant while the mean interval was varied. Rate of responding was a monotonically increasing, negatively accelerated function of rate of reinforcement over a range from 8.4 to 300 reinforcements per hour. The rate of responding also increased as time passed within the individual intervals of a given schedule. In Exp. 2 and 3, several variable-interval schedules made up of different sequences of intervals were examined. In each schedule, the rate of responding at a particular time within an interval was shown to depend at least in part on the local rate of reinforcement at that time, derived from a measure of the probability of reinforcement at that time and the proximity of potential reinforcements at other times. The functional relationship between rate of responding and rate of reinforcement at different times within the intervals of a single schedule was similar to that obtained across different schedules in Exp. 1. Experiments 4, 5, and 6 examined fixed-interval and two-valued (mixed fixed-interval fixed-interval) schedules, and demonstrated that reinforcement at one time in an interval had substantial effects on responding maintained at other times. It was concluded that the rate of responding maintained by a given interval schedule depends not on the overall rate of reinforcement provided but rather on the summation of different local effects of reinforcement at different times within intervals.     

Human aggressive responses maintained by avoidance or escape from point loss.

During 50-min sessions, 6 male human subjects could press either Button A or Button B available as nonreversible options. Button A presses were nonaggressive responses and earned points according to a fixed-ratio 100 schedule. Prior to the experiment subjects were instructed that every 10 (fixed-ratio 10) Button B presses (aggressive responses) subtracted a point from a fictitious 2nd subject. A random-time schedule of point loss was used to engender aggressive responding. The instructions attributed these point losses to the Button B presses of the subject's fictitious partner. Aggressive responding either escaped or avoided point loss by initiating an interval free of point loss. The duration of the interval was varied systematically across sessions. Avoidance contingencies maintained a high rate of aggressive responding over 30 sessions in the absence of point loss. Escape contingencies also maintained aggressive responding across sessions, with rates of aggressive responding corresponding to rates of point loss.     

Human performance on negative slope schedules of points exchangeable for money: a failure of molar maximization

Panel pressing was generated and maintained in 5 adult humans by schedules of points exchangeable for money. Following exposure to a variable-interval 30-s schedule and to a linear variable-interval 30-s schedule (which permitted points to accumulate in an unseen "store" in the absence of responding), subjects were exposed to a series of conditions with a point-subtraction contingency arranged conjointly with the linear variable-interval schedule. Specifically, points were added to the store according to the linear-variable interval 30-s schedule and were subtracted from the store according to a ratio schedule. Ratio value varied across conditions and was determined individually for each subject such that the subtraction contingency would result in an approximately 50% reduction in the rate of point delivery. Conditions that included the subtraction contingency were termed negative slope schedules because the feedback functions were negatively sloped across all response rates greater than the inverse of the variable-interval schedule, in this case, two per minute. Overall response rates varied inversely with the subtraction ratio, indicating sensitivity to the negative slope conditions, but were in excess of that required by accounts based on strict maximization of overall reinforcement rate. Performance was also not well described by a matching-based account. Detailed analyses of response patterning revealed a consistent two-state pattern in which bursts of high-rate responding alternated with periods of prolonged pausing, perhaps reflecting the joint influence of local and overall reinforcement rates.     

Elimination of reinforced behavior: intermittent schedules of not-responding

Pigeons' key pecking resulted in food according to either a variable-ratio or a variable-interval schedule. At the same time, food was available for not pecking for a specified time. The required time of not-pecking was segmented into not-responding units, and these units were followed by food according to a fixed-ratio schedule. Both unit duration and the number required were varied. In general, the shorter the time unit or the smaller the ratio, the lower was response rate. When total required not-responding time was constant, but changes in unit duration and the number required altered how the total was achieved, shorter units produced lower rates. Other conditions involved substitution of food delivered independent of responding for the not-responding schedule. With low and moderate total times to food presentation, the not-responding schedule produced lower rates; with the longest times, the response-independent schedule generated less responding. When considered in terms of relative frequency of food presentation available from a source other than pecking, the not-responding schedule reduced rate more effectively than did the response-independent schedule. Comparisons with other research suggested that food presented dependent on not responding compared favorably with punishment as a procedure for reducing response rate. Transient effects differed. Although punishment temporarily depresses rate when first imposed and temporarily enhances it when first removed, food given for not responding quickly generated steady-state rates.     

Negative behavioral contrast on multiple treadle-press schedules

Eight pigeons pressed treadles for food reinforcers delivered by several multiple variable-interval schedules. The rate of reinforcement for responding during one component schedule was held constant at 30 reinforcers per hour. The rate of reinforcement for responding during the other component varied from 0 to 120 or 240 reinforcers per hour. The schedules were presented in different orders for different subjects. The rate of responding emitted during the variable component schedule varied directly with the rate of reinforcement it provided. The rate of responding during the constant component did not increase consistently when the rate of reinforcement obtained from the variable component decreased from 30 to 0 reinforcers per hr. The rate of responding emitted during the constant component decreased when the rate of reinforcement obtained from the variable component increased from 30 reinforcers per hour to a higher rate. That is, negative but not positive behavioral contrast occurred. The failure to find positive contrast is consistent with one of the predictions of the additive theories of behavioral contrast. Finding negative contrast has ambiguous implications for the additive theories.     

Some effects of frustration in a free responding operant situation

In several experiments, rats and pigeons were reinforced on a chained schedule which varied in its second component but which always had a variable interval schedule as its first component. Occasionally, the reward which normally followed responding in the second component was omitted. On these frustrative non-reward occasions responding immediately subsequent to non-reward was sometimes elevated and sometimes depressed. The relevance of the elevation and depression effects to behavioural measures of frustration in the double runway was discussed.     

Responding maintained by the opportunity to attack during an interval food reinforcement schedule

Pigeons responded in a two-key situation. Responses on the right key (food key) were reinforced with food presentation on a response-initiated fixed-interval schedule, (i.e., first response after a fixed period of time was reinforced); responses on the left key (target key) were reinforced on a fixed-ratio schedule (i.e., every nth response was reinforced) with the presentation of a target bird that could be attacked. When the interval value of the food reinforcement schedule was varied from 1 min to 5 min, both the rate of attack responding on the target bird and the rate of responding on the target key were a function of the interval value. Responding on the target key was not maintained by the stimulus change associated with target availability, and was successively extinguished and reconditioned by removing and returning the target bird to the restraining box. When food was delivered independently of behavior, responding on the target key either remained unchanged or decreased, but was not eliminated. Responding on the target key was not maintained in the absence of an intermittent schedule of food presentation.     

Effects of conditioned reinforcement frequency in an intermittent free-feeding situation,

Key-pecking intermittently produced a set of brief exteroceptive stimulus changes under two-component multiple schedules of conditioned reinforcement. Throughout the study, free access to grain was concurrently provided on an intermittent basis via a variable-interval tape. Free food presentations scheduled by the tape were delivered if no peck had been emitted for 6 sec, and the brief stimulus changes produced by responding under the multiple schedules were those which accompanied food presentation. The second component of each multiple schedule was always associated with a 1-min, variable-interval schedule of conditioned reinforcement. The schedule associated with the first component was systematically varied and conditioned reinforcement was either absent (extinction) or programmed on a 1-, 3-, 6-, or 12-min variable-interval schedule. Under these conditions, rate of responding in the manipulated component decreased monotonically with a decrease in the frequency of conditioned reinforcement. In addition, contrast effects were often obtained in the constant, second component. These results are similar to those obtained with similar multiple schedules of primary reinforcement.     

Response allocation to concurrent fixed-ratio reinforcement schedules with work requirements by adults with mental retardation and typical preschool children.

The present experiments examined the effect of work requirements in combination with reinforcement schedule on the choice behavior of adults with mental retardation and preschool children. The work requirements of age-appropriate tasks (i.e., sorting silverware, jumping hurdles, tossing beanbags) were manipulated. Participants were presented with their choice of two response options for each trial that varied simultaneously on both work requirement and reinforcement schedule. Results showed that when responding to both choices occurred on the same reinforcement schedule, participants allocated most of their responses to the option with the easier work requirement. When the response option requiring less work was on a leaner reinforcement schedule, most participants shifted their choice to exert more work. There were individual differences across participants regarding their pattern of responding and when they switched from the lesser to the greater work requirement. Data showed that participants' responding was largely controlled by the reinforcement received for responding to each level of work. Various conceptualizations regarding the effects of work requirements on choice behavior are discussed.     

Matching and contrast on several concurrent treadle-press schedules

Four White King pigeons pressed treadles for food reinforcement on several concurrent variable-interval variable-interval schedules. The rate of reinforcement available for responding in one of the two component schedules was held constant at 30 reinforcers per hour. The rate of reinforcement available for responding in the other was varied from 120 to 60 to 15, and then to 30 reinforcers per hour. The relative rate of responding in each component schedule equalled the relative rate of reinforcement that the component provided. And, behavioral contrast, defined as an inverse relationship between the rate of responding in the constant component and the rate of reinforcement obtained by responding in the other component, occurred for all schedules.