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Bizo, Lewis
- PublicationEffects of schedules of reinforcement on the variability of location(New Zealand Association for Behaviour Analysis (NZABA), 2012)
;Neshausen, Leanne M ;McEwan, James SA handful of studies have examined the relationship between schedules of reinforcement and behavioural variability, with mixed results. The present study compares a greater range of schedules, examining the effects on location variability. Hens worked in an operant chamber containing five, horizontally arranged and active response keys. Experiment 1 compared eight schedules: FR 40, FR 10, FI (yoked FR 40), FI (yoked FR 10), VR 40, VR 10, VI (yoked VR 40) and VI (yoked VI 10). Experiment 2 compared a series of DRL schedules: 0.5 s to DRL 19.2 s, incrementing in step sizes of 20%. Location variability was measured as the percentage of switching across keys from within trials, between trials (switching from the reinforced response location to the first response location of the following trial), and the number of keys used. Results from Experiment 1 suggested no relation between schedules and location variability. However a relation between response rate and location variability was found; faster response rates resulted in less variability. Experiment 2, in attempt to control for response rate, found no relation between response rate and location variability. Switches within trials occurred more frequently in Experiment 2 than in Experiment 1, an aspect that needs further examination. - PublicationMotivating operations and animal welfare(New Zealand Association for Behaviour Analysis (NZABA), 2012)
;Jackson, Surrey; ;Foster, T MaryMcEwan, James SManipulation of unconditioned Motivating Operations (MOs) such as pain, food and water deprivation and the lowering of body weight can be potentially harmful and distressing to animals. Past research that has manipulated such MOs in order to motivate animals to respond for reinforcers is reviewed and directions for future research are discussed. The focus is on the extent that potentially distressing MO's need to be altered in order to change motivation for reinforcers in animals. In addition research directions for investigating alternative MOs that can motivate animals to respond for reinforcers are discussed. - PublicationExamining the effect of reinforcement on behaviour variability over multiple dimensions in humans(New Zealand Association for Behaviour Analysis (NZABA), 2012)
;Kong, Xiuyan ;McEwan, James S ;Foster, T MaryThe independence of dimensions of operant responses by humans was investigated in two experiments using a computerized rectangle drawing task from Ross and Neuringer (2002). Variability on the dimensions of area, shape and location was required for reinforcement for one group (VAR); and variability was not required for the other (YOKE). For all three dimensions, U-values, a measure of variability, were higher for the VAR group than for YOKE group; and the number of trials that met the criteria for reinforcement was higher for the VAR group than for the YOKE group. In Experiment 2, reinforcement was contingent on variability on two dimensions regardless of variability on the third. Participants were divided into three groups; each group had one dimension that was not required to vary. U-values were higher for dimensions when reinforcement was contingent on varying shape and location, or area and location. However, U-values did not differ significantly across dimensions when reinforcement was contingent on varying just area and shape. The results of Experiment 1 and 2 are broadly consistent with those of Ross and Neuringer (2002). The importance of orthogonality of dimensions on this task will be discussed. - PublicationAn Analysis of U-Value as a Measure of Variability
The variability in behavior has frequently been assessed using a measure known as the U-value. Of concern in this article were the limits and constraints on U-value as a measure of variability. The relation between the U-value and aspects of variability was examined using three sets of simulated data. Our analysis demonstrates that the U-value as a measure of variability on its own fails to capture repetitive patterns in the sequence of responding. The U-value was shown to reflect the evenness of the distributions of responses across the categories/options used; however, when the number of categories actually used by the participant differed from the total number available, the relation between U-values and the number of categories allocated with responses was shown to be nonlinear. It was also shown that the same value of U can represent different levels of evenness in response distributions over categories, depending on the number of categories/options actually used. These constraints and limitations are discussed in relation to how researchers might report on behavioral variability.
- PublicationBehavioural variability(New Zealand Association for Behaviour Analysis (NZABA), 2013)
;Doolan, Kathleen E; McEwan, James SThe added reinforcement of variable responding will facilitate the learning of a difficult target sequence in rats, however, the added requirement of variability has been shown to impede difficult sequence learning in humans. The present study aimed to explore the notion of sequence difficulty in humans by manipulating sequence length (6-12 items). Eighty participants were randomly allocated to one of two groups: Control and Variable. In the control conditions sequences were only reinforced if they were the target sequence, in the variability conditions sequences were concurrently reinforced on a Variable Interval 60-s schedule if the just entered sequence met a variability criterion. For the six-item sequence (122121) the Control group were most likely to produce the target sequence, while for the twelve digit sequence (221112211121) there was no difference between the two groups. The Variable group were most likely to produce the target sequence for the intermediate nine-digit sequence (112212121).The use of sequence length as a definition of sequence difficulty in both the current and previous studies are discussed. - PublicationGeneralization of learned variability across multiple dimensions in humans
This study examined whether trained variability would generalize across dimensions of the target response. Two experiments used a computerized rectangle drawing task that required participants to click and drag a mouse cursor to create rectangles on a computer screen. In Experiment 1, one group received points when successive rectangles varied in their size, shape and location (VAR), another group were yoked to the VAR group and received points that were allocated to them using a yoking procedure (YOKE), regardless of the variability in the size, shape or location of the rectangle drawn. Variability was higher for a dimension when variability on that dimension was directly reinforced. In Experiment 2, three groups of participants received points when rectangles varied on two dimensions; each group differed in the two dimensions that required variation. Variability was again higher for the reinforced dimensions for two of the three groups. Comparison with the YOKE group showed that the variability on those dimensions where variability was not directly reinforced was affected by reinforcement for variability on the other dimensions. Specifically, the variability in Shape and Location was significantly higher when these two dimensions occurred with other dimensions where variability was reinforced (as in Experiment 2) compared to when they were not required to vary (as in the YOKE group). This suggests that, for these two groups, the reinforced variability on the other two dimensions generalized to the third dimension. Implications of this finding to our understanding of factors that promote behavioral variability are discussed.
- PublicationTemporal discrimination in the canine(New Zealand Association for Behaviour Analysis (NZABA), 2013)
;Kelmere, Jessica; McEwan, James SEffective dog training depends on timely delivery of rewards. Critical to an understanding of "timely" for dogs is an understanding of the psychophysical performance of dogs when temporal durations are used as stimuli. Fifteen dogs were tested, food was used as reinforcers, and owners were asked not to feed their dogs before testing. The dogs were shown a white light for either a short or long duration, on the centre of the display. They were trained to nuzzle the lever above the screen whose colour is associated with the duration shown, for example touch the red screen lever when it was a 1 sec duration and the green screen lever when it was 4 sec. The location of the comparison stimuli was randomised across the left and right sides. Across the pairs of delays, difference in delays was one to four. If dogs made the correct response a piece of food is delivered. Once the dog responded with above 80% accuracy the testing phase began. During testing the two original signal durations were presented on 25% of trials on the remaining trials intermediate duration e.g. 6 sec are presented. Psychometric functions from stimulus-generalization sessions, when novel test durations were introduced, are presented.