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We investigated the effects of differential and nondifferential reinforcers on divided control by compound‐stimulus dimensions. Six pigeons responded in a delayed matching‐to‐sample procedure in which a blue or yellow sample stimulus flashed on/off at a fast or slow rate, and subjects reported its color or alternation frequency. The dimension to report was unsignaled (Phase 1) or signaled (Phase 2). Correct responses were reinforced with a probability of.70, and the probability of reinforcers for errors varied across conditions. Comparison choice depended on reinforcer ratios for correct and incorrect responding; as the frequency of error reinforcers according to a dimension increased, control (measured by log d) by that dimension decreased and control by the other dimension increased. Davison and Nevin's (1999) model described data when the dimension to report was unsignaled, whereas model fits were poorer when it was signaled, perhaps due to carryover between conditions. We are the first to test this quantitative model of divided control with reinforcers for errors and when the dimension to report is signaled; hence, further research is needed to establish the model's generality. We question whether divided stimulus control is dimensional and suggest it may instead reflect joint control by compound stimuli and reinforcer ratios. [ABSTRACT FROM AUTHOR]

Organisms may sometimes behave as if a contingency exists between behavior and consequences, even if this is not actually the case. Killeen (1978) suggested that such superstition occurs because of factors that bias subjects to behave "superstitiously" rather than because of failures of discrimination. We systematically replicated Killeen's experiment and compared contingency discrimination between different consequences. Six pigeons responded in a matching‐to‐sample procedure in which a response‐independent or response‐dependent stimulus change, food delivery, or blackout occurred. The pigeons reported whether the consequence was response dependent or response independent by choosing between two side keys. Discrimination was strongest after stimulus changes, weaker after blackouts, and weakest after food deliveries. These differences persisted even after additional training, suggesting asymmetries that may reflect differences in the disruptive effects of different consequences on remembering and/or behavioral mnemonics. Importantly, the pigeons were not biased to report response‐dependent consequences unless that response was consistent with locational biases; that is, they behaved "superstitiously" when there was a reason to be biased to do so. These findings corroborate Killeen's and demonstrate that behavior may deviate from contingencies not necessarily because subjects cannot discriminate those contingencies but because they are biased to behave otherwise. [ABSTRACT FROM AUTHOR]

Stimulus overselectivity describes strong control by one stimulus element at the expense of other equally relevant elements. Research suggests that control by underselected stimuli emerges following extinction of the overselected stimulus ("revaluation") and the emergence is larger when overselectivity is greater. We compared such revaluation effects with a control compound or condition in two experiments. Human participants chose between compound S+ and S‐ stimuli. Then, to assess control by compound‐stimulus elements, participants chose between individual elements in a testing phase without feedback. The S+ element chosen most often (the overselected element) underwent revaluation, during which choice of that element was extinguished and choice of a novel element reinforced. Thereafter, participants completed a retesting phase. Revaluation reduced choice of the overselected element. Choice of the underselected element decreased for participants with low overselectivity but increased for participants with high overselectivity. This was not the case for a control compound that did not undergo revaluation (Experiments 1 and 2) or in a control condition in which the overselected element continued to be reinforced during revaluation (Experiment 2). These findings suggest that overselectivity levels may modulate revaluation effects, and they also highlight the importance of the contingency change in postrevaluation changes in stimulus control. [ABSTRACT FROM AUTHOR]

It is widely assumed that reinforcers are biologically relevant stimuli, or stimuli that have been associated with biologically relevant stimuli. However, brief, arbitrary stimuli have also been reported to have reinforcement‐like effects, despite being unrelated to biologically relevant stimuli like food. The present study explored the potential reinforcement‐like effects of brief stimuli across 5 experiments. In Experiments 1 through 4, pigeon subjects responded for food reinforcement and brief stimulus presentations in a 2‐component multiple schedule. Neither baseline response rates nor resistance to change during disruption tests were systematically greater in a component with versus without brief stimulus presentations. Increasing the rate and duration of brief stimulus presentations in Experiment 4 did not reveal reinforcement‐like effects when compared directly with food. In Experiment 5, pigeons chose between independent terminal links in a concurrent‐chains procedure. Across conditions, varying the location, duration, and rate of brief stimulus presentations in the terminal links had no systematic effects on preference. In contrast, varying rates of food reinforcers resulted in large and reliable shifts in preference. Therefore, the present study found no systematic evidence that brief stimuli unrelated to food reliably increase response rates, resistance to change, or preference. These data demonstrate the value of systematic replication, and a behavioral momentum approach to assessing potential reinforcement‐like effects. [ABSTRACT FROM AUTHOR]

We present a systematic review and a meta‐analysis comparing the differential outcomes procedure to a nondifferential outcomes procedure among clinical and nonclinical populations. Sixty distinct experiments were included in the systematic review, 43 of which were included in the meta‐analysis. We calculated pooled effect sizes for accuracy (overall accuracy, test accuracy, transfer accuracy) and acquisition outcomes (latency, errors, and trials to mastery). The meta‐analysis revealed significant medium‐to‐large effect sizes for all three accuracy measures (pooled effect size range, 0.57 to 1.30). We found relatively greater effect sizes among clinical populations (effect size = 1.04). The single‐subject experimental literature included in the systematic review was consistent with the findings from the group studies, demonstrating improvements in accuracy and speed of learning for the majority of participants. Moderator and subgroup analyses suggest that discrimination difficulty may induce relatively larger differential outcomes effects. The results indicate that the differential outcomes procedure can be a valuable addition to reinforcement‐based interventions. [ABSTRACT FROM AUTHOR]

We introduce to behavior analysis a way of analyzing choice behavior that exploits recent developments in nanoeconomics, financial economics, and econometrics. A response return, modeled on an economic return, is the log differenced count of responses allocated to each of two alternatives during a short time window, compared with that in the immediately preceding window. The response return is a new dependent variable which offers a novel and useful way of looking at operant behavior, especially at the molecular level of analysis. The response–return series is a near‐instantaneous measure of an organism's dynamic preferences for each of two alternatives. Analyzing such a series requires time‐analytic techniques, including Auto‐Regressive Conditional Heteroskedastic (ARCH) models. We illustrate these techniques by analyzing choices between combinations of arithmetic and exponential variable‐interval schedules with pigeon subjects. All response–return series were well‐fitted by one of three ARCH‐family models. The fitted models were differentially sensitive to transition versus steady‐state data samples. The particular insights that the ARCH analyses offer are improved understanding of the effects of the instantaneous effects of reinforcers and their absence, of how the distribution of reinforcers in time affects choice, and of the differences between choice in transition and at steady state. [ABSTRACT FROM AUTHOR]

We advocate for rank‐permutation tests as the best choice for null‐hypothesis significance testing of behavioral data, because these tests require neither distributional assumptions about the populations from which our data were drawn nor the measurement assumption that our data are measured on an interval scale. We provide an algorithm that enables exact‐probability versions of such tests without recourse to either large‐sample approximation or resampling approaches. We particularly consider a rank‐permutation test for monotonic trend, and provide an extension of this test that allows unequal number of data points, or observations, for each subject. We provide an extended table of critical values of the test statistic for this test, and both a spreadsheet implementation and an Oracle® Java Web Start application to generate other critical values at https://sites.google.com/a/eastbayspecialists.co.nz/rank-permutation/. [ABSTRACT FROM AUTHOR]

A multivariate analysis is concerned with more than one dependent variable simultaneously. Models that generate event records have a privileged status in a multivariate analysis. From a model that generates event records, we may compute predictions for any dependent variable associated with those event records. However, because of the generality that is afforded to us by these kinds of models, we must carefully consider the selection of dependent variables. Thus, we present a conditional compromise heuristic for the selection of dependent variables from a large group of variables. The heuristic is applied to McDowell's Evolutionary Theory of Behavior Dynamics (ETBD) for fitting to a concurrent variable‐interval schedule in‐transition dataset. From the parameters obtained from fitting ETBD, we generated predictions for a wide range of dependent variables. Overall, we found that our ETBD implementation accounted well for various flavors of the log response ratio, but had difficulty accounting for the overall response rates and cumulative reinforcer effects. Based on these results, we argue that the predictions of our ETBD implementation could be improved by decreasing the base response probabilities, either by increasing the response latencies or by decreasing the sizes of the operant classes. [ABSTRACT FROM AUTHOR]

The study and use of punishment in behavioral treatments has been constrained by ethical concerns. However, there remains a need to reduce harmful behavior unable to be reduced by differential‐reinforcement procedures. We investigated whether response‐contingent presentation of a negative discriminative stimulus previously correlated with an absence of reinforcers would punish behavior maintained by positive reinforcers. Across four conditions, pigeons were trained to discriminate between a positive discriminative stimulus (S+) signaling the presence of food, and a negative discriminative stimulus (S‐) signaling the absence of food. Once learned, every five responses on average to the S+ produced S‐ for a duration of 1.5 s. S+ response rate decreased for a majority of pigeons when responses produced S‐, compared to when they did not, or when a neutral control stimulus was presented. In Condition 5, choice between two concurrently presented S+ alternatives shifted away from the alternative producing S‐, despite a 1:1 reinforcer ratio. Therefore, presenting contingent S‐ stimuli punishes operant behavior maintained on simple schedules and in choice situations. Development of negative discriminative stimuli as punishers of operant behavior could provide an effective approach to behavioral treatments for problem behavior and subverting suboptimal choices involved in addictions. [ABSTRACT FROM AUTHOR]

Models that generate event records have very general scope regarding the dimensions of the target behavior that we measure. From a set of predicted event records, we can generate predictions for any dependent variable that we could compute from the event records of our subjects. In this sense, models that generate event records permit us a freely multivariate analysis. To explore this proposition, we conducted a multivariate examination of Catania's Operant Reserve on single VI schedules in transition using a Markov Chain Monte Carlo scheme for Approximate Bayesian Computation. Although we found systematic deviations between our implementation of Catania's Operant Reserve and our observed data (e.g., mismatches in the shape of the interresponse time distributions), the general approach that we have demonstrated represents an avenue for modelling behavior that transcends the typical constraints of algebraic models. [ABSTRACT FROM AUTHOR]

Organisms that behave so as to forfeit a relatively higher overall rate of reinforcement in favor of a relatively lower rate are said to engage in suboptimal choice. Suboptimal choice has been linked with maladaptive behavior in humans. Melioration theory offers one explanatory framework for suboptimal choice. Melioration theory suggests behavior is controlled by differences in local reinforcer rates between alternatives. Vaughan (1981) arranged two experimental conditions in which maximizing the overall rate of reinforcement required behavior that was compatible, or incompatible, with melioration. Vaughan found pigeons allocated more time to a locally richer alternative even when doing so resulted in suboptimal choice. However, Vaughan did not show whether these effects could systematically reverse and did not provide within-session data to show that choice across short time spans remains under the control of differences in local reinforcer rates. The present study used pigeons to replicate and extend Vaughan's findings. We investigated shifts in overall- and within-session choice across repeated conditions, according to arranged local contingencies. Behavior systematically followed changes in local contingencies for most pigeons. Within-session data suggests that, providing differences in local reinforcer rates are discriminated, pigeons will allocate more time to a locally richer alternative, even if this leads to suboptimal choice. These findings facilitate the more confident use of similar procedures that investigate how melioration contributes to suboptimal choice. [ABSTRACT FROM AUTHOR]

Choosing the appropriate response given the circumstance is integral to all aspects of human behavior. One way of elucidating the mechanisms of choice is to relate behavior to neural correlates. Electrophysiological evidence implicates the ERP feedback-negativity (FN) and the P300 as promising neural correlates of reward processing, an integral component of learning. However, prior research has not adequately addressed how the development of a preference to select one option over another (choice preference) relates to the FN and the P300. We assessed whether variation in choice preference predicted the FN and P300 amplitude within subjects. We used a discrete-trials two-alternative choice procedure, where the reinforcer rate for each option was dependently scheduled by a concurrent variable interval. The reinforcer ratio for selecting each option was varied between sessions. Choice was quantified using both the generalized matching law sensitivity and the log odds of staying on the same versus switching to the other alternative (stay preference). The relationship between stay preference, FN, and P300 amplitudes was assessed using the innovative application of hierarchical Bayesian linear regression. The results demonstrate that stay preference was controlled by the reinforcer ratios and credibly predicted the FN amplitude but not P300 amplitude. The findings are consistent with the view that reinforcers may guide behavior by what they signal about future reinforcement, with the FN related to such a process. [ABSTRACT FROM AUTHOR]

The differential outcomes procedure uses reinforcement unique to each alternative in a conditional discrimination, leading to faster and more accurate learning relative to non-differential outcomes procedures. In this study, the differential outcomes procedure was used to teach novel tacts of musical instrument sounds to children with autism. For one set of instruments, response-specific reinforcers were used in combination with social reinforcement. For the other set, reinforcers were provided non-differentially. Two out of three participants showed enhanced learning in the differential outcomes condition, providing some support of the differential outcomes procedures as a useful tool for teaching individuals with autism. Future research into the differential outcomes effect is warranted to identify the procedural and individual factors that predict its effectiveness. [ABSTRACT FROM AUTHOR]

The extent to which a stimulus exerts control over behavior depends largely on its informativeness. However, when reinforcers have discriminative properties, they often exert less control over behavior than do other less reliable stimuli such as elapsed time. We investigated why less reliable cues in the present often overshadow stimulus control by more reliable cues presented in the recent past, by manipulating the reliability and duration of stimulus presentations. Five pigeons worked on a modified concurrent schedule in which the location of the response that produced the last reinforcer was a discriminative stimulus for the likely time and location of the next reinforcer. In some conditions, either the location of the previous reinforcer, or the location of the next reinforcer, was signaled by a red key light. This stimulus was either Brief, occurring for 10 s starting a fixed time after the most recent reinforcer, or Extended, being present at all times between food deliveries. Brief and Extended stimuli that signaled the same information had a similar effect on choice when they were present, but control by Brief stimuli weakened as time since stimulus offset elapsed. Control was divided among stimuli in the present and recent past according to the apparent reliability of the information signaled about the next reinforcer. More reliable stimuli in the present degraded, but did not erase, control by less reliable stimuli presented in the recent past. Thus, we conclude that less reliable stimuli in the present control behavior to a greater degree than do more reliable stimuli in the recent past because these more reliable stimuli are forgotten, and hence their relation to the likely availability of food cannot be discriminated. [ABSTRACT FROM AUTHOR]

In concurrent schedules, reinforcers are often followed by a brief period of heightened preference for the just-productive alternative. Such 'preference pulses' may reflect local effects of reinforcers on choice. However, similar pulses may occur after nonreinforced responses, suggesting that pulses after reinforcers are partly unrelated to reinforcer effects. McLean, Grace, Pitts, and Hughes (2014) recommended subtracting preference pulses after responses from preference pulses after reinforcers, to construct residual pulses that represent only reinforcer effects. Thus, a reanalysis of existing choice data is necessary to determine whether changes in choice after reinforcers in previous experiments were actually related to reinforcers. In the present paper, we reanalyzed data from choice experiments in which reinforcers served different functions. We compared local choice, mean visit length, and visit-length distributions after reinforcers and after nonreinforced responses. Our reanalysis demonstrated the utility of McLean et al.'s preference-pulse correction for determining the effects of reinforcers on choice. However, visit analyses revealed that residual pulses may not accurately represent reinforcer effects, and reinforcer effects were clearer in visit analyses than in local-choice analyses. The best way to determine the effects of reinforcers on choice may be to conduct visit analyses in addition to local-choice analyses. [ABSTRACT FROM AUTHOR]

Discrete ‐ trial teaching is a strategy frequently used to teach functional skills to individuals with developmental and intellectual disabilities. Research has shown that the within ‐ trial components of the procedure should be administered with ≥90% treatment integrity to facilitate optimal learning. Usually within ‐ trial treatment integrity is measured using whole ‐ session methods such as percentage of trials correctly administered. This study demonstrated one ‐ step Markov transition matrices as a method of assessing within ‐ trial treatment integrity. All components of discrete trials were coded and time ‐ stamped from video recordings of therapist–learner dyads in their typical setting (home or school). Several types of within ‐ trial treatment integrity errors were identified using the Markov transition matrices, error sequences that could not be identified using a percentage correct analysis. Better identification of errors has the potential both to enhance treatment integrity and to gain efficiency by targeted retraining of therapists. Copyright © 2016 John Wiley & Sons, Ltd. [ABSTRACT FROM AUTHOR]

The baseline rate of a reinforced target response decreases with the availability of response-independent sources of alternative reinforcement; however, resistance to disruption and relapse increases. Because many behavioral treatments for problem behavior include response-dependent reinforcement of alternative behavior, the present study assessed whether response-dependent alternative reinforcement also decreases baseline response rates but increases resistance to extinction and relapse. We reinforced target responding at equal rates across two components of a multiple schedule with pigeons. We compared resistance to extinction and relapse via reinstatement of (1) a target response trained concurrently with a reinforced alternative response in one component with (2) a target response trained either concurrently or in separate components from the alternative response across conditions. Target response rates trained alone in baseline were higher but resistance to extinction and relapse via reinstatement tests were greater after training concurrently with the alternative response. In another assessment, training target and alternative responding together, but separating them during extinction and reinstatement tests, produced equal resistance to extinction and relapse. Together, these findings are consistent with behavioral momentum theory-operant response-reinforcer relations determined baseline response rates but Pavlovian stimulus-reinforcer relations established during training determined resistance to extinction and relapse. These findings imply that reinforcing alternative behavior to treat problem behavior could initially reduce rates but increase persistence. [ABSTRACT FROM AUTHOR]

The article talks about melioration theory, a theory in psychology used as an alternative to the matching law. It informs that the theory is used as an explanation for why an organism makes choices based on the rewards or reinforcers it receives terminology and the range of procedures that constitute dependent scheduling.

Overall reinforcer rate appears to affect choice. The mechanism for such an effect is uncertain, but may relate to reinforcer rate changing the discrimination of the relation between stimuli and reinforcers. We assessed whether a quantitative model based on a stimulus-control approach could be used to account for the effects of overall reinforcer rate on choice under changing time-based contingencies. On a two-key concurrent schedule, the likely availability of a reinforcer reversed when a fixed time had elapsed since the last reinforcer, and the overall reinforcer rate was varied across conditions. Changes in the overall reinforcer rate produced a change in response bias, and some indication of a change in discrimination. These changes in bias and discrimination always occurred quickly, usually within the first session of a condition. The stimulus-control approach provided an excellent account of the data, suggesting that changes in overall reinforcer rate affect choice because they alter the frequency of reinforcers obtained at different times, or in different stimulus contexts, and thus change the discriminated relation between stimuli and reinforcers. These findings support the notion that temporal and spatial discriminations can be understood in terms of discrimination of reinforcers across time and space. [ABSTRACT FROM AUTHOR]

We investigated why violations to the constant-ratio rule, an assumption of the generalized matching law, occur in procedures that arrange frequent changes to reinforcer ratios. Our investigation produced steady-state data and compared them with data from equivalent, frequently changing procedures. Six pigeons responded in a four-alternative concurrent-schedule experiment with an arranged reinforcer-rate ratio of 27:9:3:1. The same four variable-interval schedules were used in every condition, for 50 sessions, and the physical location of each schedule was changed across conditions. The experiment was a steady-state version of a frequently changing procedure in which the locations of four VI schedules were changed every 10 reinforcers. We found that subjects' responding was consistent with the constant-ratio rule in the steady-state procedure. Additionally, local analyses showed that preference after reinforcement was towards the alternative that was likely to produce the next reinforcer, instead of being towards the just-reinforced alternative as in frequently changing procedures. This suggests that the effect of a reinforcer on preference is fundamentally different in rapidly changing and steady-state environments. Comparing this finding to the existing literature suggests that choice is more influenced by reinforcer-generated signals when the reinforcement contingencies often change. [ABSTRACT FROM AUTHOR]

Deciding on appropriate sampling to obtain representative samples of behavior is important but not straightforward, because the relative duration of the target behavior may affect its observation in a given sampling interval. Work-sampling methods, which offer a way to adjust the frequency of sampling according to a priori or ongoing estimates of the behavior to achieve a preselected level of representativeness, may provide a solution. Full-week observations of 7 behaviors were conducted for 3 students with autism spectrum disorder and intellectual disabilities. Work-sampling methods were used to select momentary time samples from the full time-of-interest, which produced representative samples. However, work sampling required impractically high numbers of time samples to obtain representative samples. More practical momentary time samples produced less representative samples, particularly for low-duration behaviors. The utility and limits of worksampling methods for applied behavior analysis are discussed. [ABSTRACT FROM AUTHOR]

When the availability of reinforcers depends on time since an event, time functions as a discriminative stimulus. Behavioral control by elapsed time is generally weak, but may be enhanced by added stimuli that act as additional time markers. The present paper assessed the effect of brief and continuous added stimuli on control by time-based changes in the reinforcer differential, using a procedure in which the local reinforcer ratio reversed at a fixed time after the most recent reinforcer delivery. Local choice was enhanced by the presentation of the brief stimuli, even when the stimulus change signalled only elapsed time, but not the local reinforcer ratio. The effect of the brief stimulus presentations on choice decreased as a function of time since the most recent stimulus change. We compared the ability of several versions of a model of local choice to describe these data. The data were best described by a model which assumed that error in discriminating the local reinforcer ratio arose from imprecise discrimination of reinforcers in both time and space, suggesting that timing behavior is controlled not only by discrimination elapsed time, but by discrimination of the reinforcer differential in time. [ABSTRACT FROM AUTHOR]

Often it is assumed that electronic recording by observers necessarily provides better quality data than pen-and-paper methods. Fifteen novice observers recorded rates of responding from 10 role-played video samples using one of three continuous recording input formats: keyboard (laptop), touchscreen (personal digital assistants), or pen-and-paper. We evaluated the quality of the observers' data compared with criterion records using calibration and interobserver agreement algorithms. Results of the calibration analysis revealed that observers in the touchscreen group produced the most consistently accurate and precise data, the keyboard group observers showed wide variation in precision and accuracy, and the pen-and-paper group observers were significantly less precise than the touchscreen group. We conclude that although electronic recording has the potential to be as accurate as, and more precise than, pen-and-paper methods, this is far from guaranteed. Analyses of observers' errors advise recommendations for improving data accuracy and precision when using each method. Copyright © 2014 John Wiley & Sons, Ltd. [ABSTRACT FROM AUTHOR]

The current experiment examined the degree to which locally varying food probabilities on two keys across time since food presentations can continue to control choice until the next food delivery. In two sets of conditions, the probability of food delivery being made available on one key relative to the other key varied sinusoidally across a 1-min period following each food delivery. In Set 1, food-probability changes were unsignaled and the number of cycles per min was varied across conditions. In Set 2, there were always two complete cycles of the sinusoid in the 1-min period, and brief key-color changes were arranged at a selection of fixed times since food delivery to signal portions of the sinusoid. In Set 1, control of choice by local probability of food on each key decreased over time since food delivery. Control by local food probabilities was greater in conditions that arranged fewer cycles per min. The onset of stimulus changes in Set 2 led to a transient reinstatement of local control by food probabilities regardless of the portion of the sinusoidal variation in food probabilities signaled by the stimuli. However, in conditions where the same colored stimuli signaled different portions of the sinusoidal variation in food-delivery probabilities, stimulus changes attenuated joint control by elapsed time and food-probability values. These results suggest that, changing relative food probabilities and stimuli can direct preference toward the likely location of the next food delivery across time since a food presentation, although the degree to which control over choice will be maintained across elapsed time depends on how experimenter-arranged contingencies are mapped onto elapsed time. [ABSTRACT FROM AUTHOR]

Six pigeons worked on concurrent exponential variable-interval schedules in which the relative frequency of food deliveries for responding on the two alternatives reversed at a fixed time after each food delivery. Across conditions, the point of food-ratio reversal was varied from 10 s to 30 s, and the overall reinforcer rate was varied from 1.33 to 4 per minute. The effect of rate of food delivery and food-ratio-reversal time on choice and response rates was small. In all conditions, postfood choice was toward the locally richer key, regardless of the last-food location. Unlike the local food ratio which changed in a stepwise fashion, local choice changed according to a decelerating monotonic function, becoming substantially less extreme than the local food ratio soon after food delivery. This deviation in choice appeared to result from the birds' inaccurate discrimination of the time of food deliveries; local choice was described well by a model that assumed that log response ratios matched food ratios that were redistributed across surrounding time bins with mean time t and a constant coefficient of variation. We suggest that local choice is controlled by the likely availability of food in time, and that choice matches the discriminated log of the ratio of food rates across time since the last food delivery. [ABSTRACT FROM AUTHOR]

Data from five experiments on choice between more than two variable-interval schedules were modeled with different equations for the Law of Effect. Navakatikyan's (2007) component-functions models with three, four and five free parameters were compared with Stevens' (1957), Herrnstein's (1970) and Davison and Hunter's (1976) equations. These latter models are consistent with the generalized-matching principle, whereas Navakatikyan's models are not. Navakatikyan's models performed better or on par with their competitors, especially in predicting residence-time data and generalized-matching sensitivities for time allocation. The models described well an observed decrease, in several of these data sets, in generalized-matching sensitivity between two alternatives when reinforcer rate increased on the other alternatives. Models built on the generalized-matching principle cannot do this. Navakatikyan's models also performed better, though to a lesser extent, than their competitors for data sets that are not obviously inconsistent with generalized matching. [ABSTRACT FROM AUTHOR]

Four pigeons performed a simultaneous matching-to-sample (MTS) task involving two samples and two comparisons that differed in their pixel density and luminance. After a long history of reinforcers for correct responses after both samples, 15 conditions arranged either continuous reinforcement of correct responses after Sample 1 and extinction for all responses after Sample 2, or vice versa. The sample after which correct responses were reinforced alternated across successive conditions. The disparity between the samples and the disparity between the comparisons were varied independently across conditions in a quasifactorial design. Contrary to predictions of extant quantitative models, which assume that MTS tasks involve two 3-term contingencies of reinforcement, matching accuracies were not at chance levels in these conditions, comparison-selection ratios differed after the two samples, and effects on matching accuracies of both sample disparity and comparison disparity were observed. These results were, however, consistent with ordinal and sometimes quantitative predictions of Jones' (2003) theory of stimulus and reinforcement effects in MTS tasks. This theory asserts that MTS tasks involve four-term contingencies of reinforcement and that any tendency to select one comparison more often than the other over a set of trials reflects meaningful differences between comparison-discrimination accuracies after the two samples. [ABSTRACT FROM AUTHOR]

Four pigeons were trained on two-key concurrent variable-interval schedules with no changeover delay. In Phase 1, relative reinforcers on the two alternatives were varied over five conditions from .1 to .9. In Phases 2 and 3, we instituted a molar feedback function between relative choice in an interreinforcer interval and the probability of reinforcers on the two keys ending the next interreinforcer interval. The feedback function was linear, and was negatively sloped so that more extreme choice in an interreinforcer interval made it more likely that a reinforcer would be available on the other key at the end of the next interval. The slope of the feedback function was 21 in Phase 2 and 23 in Phase 3. We varied relative reinforcers in each of these phases by changing the intercept of the feedback function. Little effect of the feedback functions was discernible at the local (interreinforcer interval) level, but choice measured at an extended level across sessions was strongly and significantly decreased by increasing the negative slope of the feedback function. [ABSTRACT FROM AUTHOR]

We investigated the effects of discriminative stimuli on choice in a highly variable environment using a procedure in which multiple two-key concurrent VI VI components changed every 10 reinforcers and were signaled by differential flashes of red and yellow keylights. Across conditions, five pigeons were exposed to a number of different combinations of the following component reinforcer ratios: 27:1, 9:1, 3:1, 1:1, 1:3, 1:9, 1:27. Overall, there was clear control by the component signals in that preference, early in components and particularly before any reinforcers had been delivered, was ordinally related to the signaled reinforcer ratios. In conditions in which only two components arranged unequal reinforcer ratios (e.g., 27:1 and 1:27) with the remaining components arranging 1:1 reinforcer ratios, preference before the first reinforcer in a component showed peak shift in that the most extreme preference did not occur in the unequal reinforcer-ratio components, but in 1:1 components further towards the ends of the stimulus dimension. The contingency-discriminability model (Davison & Nevin, 1999) was fitted to the data and provided an excellent description of the interactions between stimulus and reinforcer effects in a highly variable environment. [ABSTRACT FROM AUTHOR]

Sidman's (2000) theory regarding the origin of equivalence relations predicts that a reinforcing stimulus common to distinct equivalence classes must drop out of the equivalence relations. This prediction was tested in the present study by arranging class-specific reinforcers, R1 and R2, following correct responding on the prerequisite conditional discriminations (Ax-Bx, Cx-Bx) for two stimulus classes, A1B1C1 and A2B2C2. A class-common reinforcer, R3, was presented following correct responding on the prerequisite conditional discriminations for a further two stimulus classes, A3B3C3 and A4B4C4. Sidman's theory predicts reinforcer inclusion within Classes 1 and 2 only, given this training arrangement. Experiment 1 tested for the emergence of four equivalence classes and of stimulus-reinforcer and reinforcer-stimulus relations in each class. Four of the 6 subjects demonstrated the reinforcer-based relations in all four equivalence classes, rather than in only those classes with a class-specific reinforcer, as Sidman's theory predicts. One of the remaining 2 subjects showed the reinforcer-based relations in three of the four classes. Experiment 2 extended these findings to document the emergence of interclass matching relations based on the common reinforcer R3, in 5 of 6 subjects, such that a Class 3 sample-occasioned the selection of a Class 4 sample when the Class 3 comparison was absent, and similarly, a Class 4 sample occasioned the selection of a Class 3 comparison when the Class 4 comparison was absent. These interclass relations emerged despite the simultaneous maintenance of Class 3 and 4 baseline conditional discriminations, so that the Class 3 and 4 stimuli and reinforcer simultaneously were, and were not, part of a single larger equivalence class. These data are irreconcilable with Sidman's theory, and question the utility of the application of the equivalence relation in describing derived stimulus relations. [ABSTRACT FROM AUTHOR]

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. [ABSTRACT FROM AUTHOR]

Six pigeons were trained in a procedure in which sessions included seven unsignaled components, each offering two pecking keys, and each providing a potentially different reinforcer ratio between the two keys. Across conditions, various combinations of reinforcer ratios and reinforcer-magnitude ratios were used to create unequal reinforcer distributions between the two alternatives when averaged across a session. The results extended previous research using the same basic procedure that had included only reinforcer distributions symmetrical around 1:1. Data analyses suggested that the variables controlling choice operated at a number of levels: First, individual reinforcers had local effects on choice; second, sequences of successive reinforcers obtained at the same alternative (continuations) had cumulative effects; and, third, when these sequences themselves occurred with greater frequency, their effects further cumulated. A reinforcer obtained at the other alternative following a sequence of continuations (a discontinuation) had a large effect and apparently reset choice to levels approximating the sessional reinforcer ratio. [ABSTRACT FROM AUTHOR]

Five pigeons were trained on pairs of concurrent variable-interval schedules in a switching-key procedure. The arranged overall rate of reinforcement was constant in all conditions, and the reinforcer-magnitude ratios obtained from the two alternatives were varied over five levels. Each condition remained in effect for 65 sessions and the last 50 sessions of data from each condition were analyzed. At a molar level of analysis, preference was described well by a version of the generalized matching law, consistent with previous reports. More local analyses showed that recently obtained reinforcers had small measurable effects on current preference, with the most recently obtained reinforcer having a substantially larger effect. Larger reinforcers resulted in larger and longer preference pulses, and a small preference was maintained for the larger-magnitude alternative even after long inter-reinforcer intervals. These results are consistent with the notion that the variables controlling choice have both short- and long-term effects. Moreover, they suggest that control by reinforcer magnitude is exerted in a manner similar to control by reinforcer frequency. Lower sensitivities when reinforcer magnitude is varied are likely to be due to equal frequencies of different sized preference pulses, whereas higher sensitivities when reinforcer rates are varied might result from changes in the frequencies of different sized preference pulses. [ABSTRACT FROM AUTHOR]

Six pigeons responded on pairs of concurrent variable-interval schedules with, in different parts, four different arrangements of alternation between schedules. Following a single switching-key response, alternation was either strict or random, and the alternative presented after a switch (the postswitch alternative) was either signaled by the location of the switching key or unsignaled. Generalized-matching analyses showed little difference in behavior among the different alternation arrangements, except the usual finding of lower sensitivity of response allocation than time allocation was eliminated by arranging random alternation. Patterns of interchangeover times were similar for all arrangements except signaled random alternation. Differences in behavior preceding the different postswitch alternatives were found in the signaled random alternation procedure. Preference was biased towards the color of the signaled postswitch alternative and showed increased sensitivity when the postswitch alternative was to be the one with the higher reinforcer rate. Interchangeover times were substantially shorter when the postswitch alternative was signaled to be different from the current alternative than when it was signaled to be the same. However, when separate reinforcer ratios were calculated for the different postswitch alternatives, those effects were eliminated or greatly reduced. We suggest that, although behavior is indeed influenced by the postswitch alternative, the mechanism is indirect. That is, the distributions of reinforcers between alternatives obtained before each postswitch alternative differ when those alternatives are signaled, and those distributions are discriminated, but the same relations between choice and relative reinforcement hold irrespective of which postswitch alternative is signaled. [ABSTRACT FROM AUTHOR]

Examines the short-and long-term effects of reinforcers on the concurrent preference of pigeons. Analysis on the concurrent variable-interval schedules in switching-key procedure; Effects of the condition on current preference; Factors contributing to the increase of short-term effects.

Presents a study in which six pigeons were trained on their choice of concurrent variable-interval schedules in which two different travel times between alternatives, 4.5 and 0.5 seconds, were randomly arranged. Finding that dwell times on the alternatives were consistently longer in the presence of the stimulus that signaled the shorter travel time.

Compares the effect of arranging the some-patches-are-empty animal foraging paradigm in a closed economy with the well-established results obtained in open economies. Results indicating increase in patch residence time when travel time increases but is longer than optimal; Consequence of any variance or error in residence times.

Examines the effects of overall reinforcer rate and temporal distribution of reinforcers on concurrent choices of pigeons. Experimental procedure and conditions; Response and time allocation; Sensitivity of bird to reinforcer.

Discusses the results of a study on the effects of food deprivation and session duration in pigeons. Response to food reinforcement on multiple variable-interval schedules in which the total consumption of food was entirely determined by the pigeons' interaction with the schedules.

Reinforcing an alternative response in the same context as a target response reduces the rate of occurrence but increases the persistence of that target response. Applied researchers who use such techniques to decrease the rate of a target problem behavior risk inadvertently increasing the persistence of the same problem behavior. Behavioral momentum theory asserts that the increased persistence is a function of the alternative reinforcement enhancing the Pavlovian relation between the target stimulus context and reinforcement. A method showing promise for reducing the persistence-enhancing effects of alternative reinforcement is to train the alternative response in a separate stimulus context before combining with the target stimulus in extinction. The present study replicated previous findings using pigeons by showing that combining an "alternative" richer VI schedule (96 reinforcers/hr) with a "target" leaner VI schedule (24 reinforcers/hr) reduced resistance to extinction of target responding compared with concurrent training of the alternative and target responses (totaling 120 reinforcers/hr). We also found less relapse with a reinstatement procedure following extinction with separate-context training, supporting previous findings that training conditions similarly influence both resistance to extinction and relapse. Finally, combining the alternative stimulus context was less disruptive to target responding previously trained in the concurrent schedule, relative to combining with the target response trained alone. Overall, the present findings suggest the technique of combining stimulus contexts associated with alternative responses with those associated with target responses disrupts target responding. Furthermore, the effectiveness of this disruption is a function of training context of reinforcement for target responding, consistent with assertions of behavioral momentum theory.

Reinforcers may increase operant responding via a response-strengthening mechanism whereby the probability of the preceding response increases, or via some discriminative process whereby the response more likely to provide subsequent reinforcement becomes, itself, more likely. We tested these two accounts. Six pigeons responded for food reinforcers in a two-alternative switching-key concurrent schedule. Within a session, equal numbers of reinforcers were arranged for responses to each alternative. Those reinforcers strictly alternated between the two alternatives in half the conditions, and were randomly allocated to the alternatives in half the conditions. We also varied, across conditions, the alternative that became available immediately after a reinforcer. Preference after a single reinforcer always favored the immediately available alternative, regardless of the local probability of a reinforcer on that alternative (0 or 1 in the strictly alternating conditions, .5 in the random conditions). Choice then reflected the local reinforcer probabilities, suggesting some discriminative properties of reinforcement. At a more extended level, successive same-alternative reinforcers from an alternative systematically shifted preference towards that alternative, regardless of which alternative was available immediately after a reinforcer. There was no similar shift when successive reinforcers came from alternating sources. These more temporally extended results may suggest a strengthening function of reinforcement, or an enhanced ability to respond appropriately to "win-stay" contingencies over "win-shift" contingencies.

It has long been understood that food deliveries may act as signals of future food location, and not only as strengtheners of prefood responding as the law of effect suggests. Recent research has taken this idea further--the main effect of food deliveries, or other "reinforcers", may be signaling rather than strengthening. The present experiment investigated the ability of food deliveries to signal food contingencies across time after food. In Phase 1, the next food delivery was always equally likely to be arranged for a left- or a right-key response. Conditions were arranged such that the next food delivery was likely to occur either sooner on the left (or right) key, or sooner on the just-productive (or not-just-productive) key. In Phase 2, similar contingencies were arranged, but the last-food location was signaled by a red keylight. Preference, measured in 2-s bins across interfood intervals, was jointly controlled by the likely time and location of the next food delivery. In Phase 1, when any food delivery signaled a likely sooner next food delivery on a particular key, postfood preference was strongly toward that key, and moved toward the other key across the interreinforcer interval. In other conditions in which food delivery on the two keys signaled different subsequent contingencies, postfood preference was less extreme, and quickly moved toward indifference. In Phase 2, in all three conditions, initial preference was strongly toward the likely-sooner food key, and moved to the other key across the interfood interval. In both phases, at a more extended level of analysis, sequences of same-key food deliveries caused a small increase in preference for the just-productive key, suggesting the presence of a "reinforcement effect", albeit one that was very small.

Conditioned reinforcer effects may be due to the stimulus' discriminative rather than its strengthening properties. While this was demonstrated in a frequently-changing choice procedure, a single attempt to replicate in a relatively static choice environment failed. We contend that this was because the information provided by the stimuli was nonredundant in the frequently-changing preparation, and redundant in the steady-state arrangement. In the present experiments, 6 pigeons worked in a steady-state concurrent schedule procedure with nonredundant informative stimuli (red keylight illuminations). When a response-contingent red keylight signaled that the next food delivery was more likely on one of the two alternatives, postkeylight choice responding was reliably for that alternative. This effect was enhanced after a history of extended informative red keylight presentation (Experiment 2). These results lend support to recent characterizations of conditioned reinforcer effects as reflective of a discriminative, rather than a reinforcing, property of the stimulus.

We aimed to investigate whether novel stimulus relations would emerge from stimulus correlations when those relations explicitly conflicted with reinforced relations. In a symbolic matching-to-sample task using kanji characters as stimuli, we arranged class-specific incorrect comparison stimuli in each of three classes. After presenting either Ax or Cx stimuli as samples, choices of Bx were reinforced and choices of Gx or Hx were not. Tests for symmetry, and combined symmetry and transitivity, showed the emergence of three 3-member (AxBxCx) stimulus classes in 5 of 5 human participants. Subsequent tests for all possible emergent relations between Ax, Bx, Cx and the class-specific incorrect comparisons Gx and Hx showed that these relations emerged for 4 of 5 the participants after extended overtraining of the baseline relations. These emergent relations must have been based on stimulus-stimulus correlations, and were not properties of the trained discriminated operants, because they required control by relations explicitly extinguished during training. This result supports theoretical accounts of emergent relations that emphasize stimulus correlation over operant contingencies.

Four pigeons were trained on two-key concurrent variable-interval schedules with no changeover delay. In Phase 1, relative reinforcers on the two alternatives were varied over five conditions from .1 to .9. In Phases 2 and 3, we instituted a molar feedback function between relative choice in an interreinforcer interval and the probability of reinforcers on the two keys ending the next interreinforcer interval. The feedback function was linear, and was negatively sloped so that more extreme choice in an interreinforcer interval made it more likely that a reinforcer would be available on the other key at the end of the next interval. The slope of the feedback function was -1 in Phase 2 and -3 in Phase 3. We varied relative reinforcers in each of these phases by changing the intercept of the feedback function. Little effect of the feedback functions was discernible at the local (interreinforcer interval) level, but choice measured at an extended level across sessions was strongly and significantly decreased by increasing the negative slope of the feedback function.

Four pigeons were trained on a conditional discrimination. The conditional stimuli were compounds of pairs of stimuli from two different dimensions, fast versus slow cycles of red or green stimuli, and short- versus long-duration presentations of these cycles. Across conditions, the probability of reinforcers for correctly responding to each dimension was varied from 0 to 1. Discriminability, measured by log d, for stimuli on a dimension increased as the relative frequency of reinforcers for that dimension increased, replicating the results of Shahan and Podlesnik (2006). Two further conditions showed that discriminability between stimuli on each dimension was unaffected by whether the stimuli on the other dimension varied or were constant. Finally, maximal discriminability was unchanged in a redundant-relevant cues condition in which either of the stimuli comprising a compound signaled the same correct response. Davison and Nevin's (1999) model provided an excellent quantitative account of the effect of relative reinforcer frequency on discriminability, and thus of the way in which divided stimulus control is itself controlled by relative reinforcement.

Five pigeons responded on steady-state concurrent variable-interval variable-interval schedules of food presentation in which half of the foods were removed and replaced with nonfood stimuli. Across conditions, the stimuli were either paired or unpaired with food, and the correlation between the ratio of food deliveries on the two alternatives and the ratio of nonfood stimuli was either -1, 0, or +1. Neither the pairing of stimuli with food, nor the correlation between stimuli and food, affected generalized-matching performance, but paired stimuli had a demonstrable effect at a local level of analysis. This effect was independent of the food-stimulus correlation. These results differ from results previously obtained in a frequently changing environment. We attribute this difference in results to differences in the information value of response-contingent stimuli in frequently changing versus relatively constant environments, as well as to differences between forward pairing and simultaneous pairing of the stimuli with food.

One assumption of the matching approach to choice is that different independent variables control choice independently of each other. We tested this assumption for reinforcer rate and magnitude in an extensive parametric experiment. Five pigeons responded for food reinforcement on switching-key concurrent variable-interval variable-interval schedules. Across conditions, the ratios of reinforcer rates and of reinforcer magnitudes on the two alternatives were both manipulated. Control by each independent variable, as measured by generalized-matching sensitivity, changed significantly with the ratio of the other independent variable. Analyses taking the model-comparison approach, which weighs improvement in goodness-of-fit against increasing number of free parameters, were inconclusive. These analyses compared a model assuming constant sensitivity to magnitude across all reinforcer-rate ratios with two alternative models. One of those alternatives allowed sensitivity to magnitude to vary freely across reinforcer-rate ratios, and was less efficient than the common-sensitivity model for all pigeons, according to the Schwarz-Bayes information criterion. The second alternative model constrained sensitivity to magnitude to be equal for pairs of reinforcer-rate ratios that deviated from unity by proportionately equal amounts but in opposite directions. This model was more efficient than the common-magnitude-sensitivity model for 2 of the pigeons, but not for the other 3. An analysis of variance, carried out independently of the generalized-matching analysis, also showed a significant interaction between the effects of reinforcer rate and reinforcer magnitude on choice. On balance, these results suggest that the assumption of independence inherent in the matching approach cannot be maintained. Relative reinforcer rates and magnitudes do not control choice independently.

Sidman's (2000) theory regarding the origin of equivalence relations predicts that a reinforcing stimulus common to distinct equivalence classes must drop out of the equivalence relations. This prediction was tested in the present study by arranging class-specific reinforcers, R1 and R2, following correct responding on the prerequisite conditional discriminations (Ax-Bx, Cx-Bx) for two stimulus classes, A1B1C1 and A2B2C2. A class-common reinforcer, R3, was presented following correct responding on the prerequisite conditional discriminations for a further two stimulus classes, A3B3C3 and A4B4C4. Sidman's theory predicts reinforcer inclusion within Classes 1 and 2 only, given this training arrangement. Experiment 1 tested for the emergence of four equivalence classes and of stimulus-reinforcer and reinforcer-stimulus relations in each class. Four of the 6 subjects demonstrated the reinforcer-based relations in all four equivalence classes, rather than in only those classes with a class-specific reinforcer, as Sidman's theory predicts. One of the remaining 2 subjects showed the reinforcer-based relations in three of the four classes. Experiment 2 extended these findings to document the emergence of interclass matching relations based on the common reinforcer R3, in 5 of 6 subjects, such that a Class 3 sample occasioned the selection of a Class 4 sample when the Class 3 comparison was absent, and similarly, a Class 4 sample occasioned the selection of a Class 3 comparison when the Class 4 comparison was absent. These interclass relations emerged despite the simultaneous maintenance of Class 3 and 4 baseline conditional discriminations, so that the Class 3 and 4 stimuli and reinforcer simultaneously were, and were not, part of a single larger equivalence class. These data are irreconcilable with Sidman's theory, and question the utility of the application of the equivalence relation in describing derived stimulus relations.