On the origins of emergent differential sample behavior

Two experiments evaluated the source(s) of emergent differential sample behavior in pigeons. Initially, pigeons learned two-sample, two-alternative symbolic matching in which different patterns of sample responding were required to produce the comparisons. Afterwards, two other samples nominally identical to the comparisons were added to the matching task. On new-sample trials, completion of either sample-response requirement produced comparison alternatives which were either the same as or different from the alternatives on the familiar-sample trials. Differential responding to the new samples developed only when the comparisons were the same as the familiar samples. The results are consistent with acquired sample equivalence and adventitious reinforcement accounts of emergent sample behavior and are inconsistent with bidirectional transfer (symmetry) between the response patterns explicitly required to the originally trained (familiar) samples and the subsequently reinforced comparisons.     

Sensitization and habituation of motivated behavior in overweight and non-overweight children

The rate of habituation to food is inversely related to energy intake, and overweight children may habituate slower to food and consume more energy. This study compared patterns of sensitization, as defined by an initial increase in operant or motivated responding for food, and habituation, defined by gradual reduction in responding, for macaroni and cheese and pizza in overweight and non-overweight 8- to 12-year-old children. Non-overweight children habituated faster to both foods than overweight children (p = .03). All children recovered motivated responding for a new food (chocolate). Overweight children consumed more energy than non-overweight children (p = .0004). Children who showed a sensitization in responding consumed more food (p = .001), and sensitization moderated the effect of overweight on habituation, with slower habituation for overweight children who sensitized (p < .001). This study replicates previous data on overweight/non-overweight differences in habituation of food and energy intake, and provides new information that individual differences in sensitization and habituation of motivated responding to obtain food may be associated with a sustained motivation to eat, resulting in greater energy intake.     

An analysis of coordinated responding of pigeons

Experimental analyses of coordinated responding (i.e., cooperation) have been derived from a procedure described by Skinner (1962) in which reinforcers were delivered to a pair of subjects (a dyad) if both responded within a short interval, thus satisfying a coordination contingency. Although it has been suggested that this contingency enhances rates of temporally coordinated responding, limitations of past experiments have raised questions concerning this conclusion. The present experiments addressed some of these limitations by holding the schedule of reinforcement (Experiment 1: fixed ratio 1; Experiment 2; variable interval 20 s) constant across phases and between dyad members and by varying, in different conditions, the number of response keys (one to three) across which coordination could occur. Greater percentages of coordinated responding occurred under the coordinated-reinforcement phases than under independent-reinforcement phases in most conditions. The one exception during the one-key condition of Experiment 1 appeared to be a consequence of variability introduced by the independent-reinforcement phase procedure. Furthermore, coordination percentages decreased with increasing response options under both schedules. These results confirm and extend the finding that coordination contingencies control higher rates of temporally coordinated responding than independent-reinforcement contingencies do.     

Method effects due to social desirability as a parsimonious explanation of the deviation from unidimensionality in LOT-R scores

Dispositional optimism measured by the Life Orientation Test (Revised; LOT-R, Scheier et al., 1994) was originally proposed as a unidimensional construct pertaining to individual differences in positive outcome expectancies. However, factor analytic research has suggested two separate “optimism” and “pessimism” factors associated with positively and negatively worded items respectively. Using confirmatory factor analysis with data from N = 658 students it is shown that a general optimism model with method effects of the positively worded items fits even better than the “optimism–pessimism” model in terms of the AIC statistic, which accounts for both model parsimony and model fit. Furthermore, an attempt is made to explain the method effects by social desirability: impression management, one of two components of socially desirable responding, correlates significantly with the method factor whereas the other component, self-deceptive enhancement, is related to the general optimism factor. Thus it is shown that the deviation from unidimensionality of observed scores does not imply deviation from unidimensionality of optimism when method effects are incorporated in the model.     

THE EFFECTS OF RESPONSE CARDS ON STUDENT AND TEACHER BEHAVIOR DURING VOCABULARY INSTRUCTION

The use of response cards during whole‐class English vocabulary instruction was evaluated. Five low‐participating students were observed during hand‐raising conditions and response‐card conditions to observe the effects of response cards on student responding and test scores and teacher questions and feedback. Responding and test scores were higher for all targeted students in the response‐card condition. The teacher asked a similar number of questions in both conditions; however, she provided more feedback in the response‐card condition.     

Overt naming fMRI pre- and post-TMS: Two nonfluent aphasia patients, with and without improved naming post-TMS

Two chronic, nonfluent aphasia patients participated in overt naming fMRI scans, pre- and post-a series of repetitive transcranial magnetic stimulation (rTMS) treatments as part of a TMS study to improve naming. Each patient received 10, 1-Hz rTMS treatments to suppress a part of R pars triangularis. P1 was a ‘good responder’ with improved naming and phrase length; P2 was a ‘poor responder’ without improved naming.Pre-TMS (10 years poststroke), P1 had significant activation in R and L sensorimotor cortex, R IFG, and in both L and R SMA during overt naming fMRI (28% pictures named). At 3 mo. post-TMS (42% named), P1 showed continued activation in R and L sensorimotor cortex, R IFG, and in R and L SMA. At 16 mo. post-TMS (58% named), he also showed significant activation in R and L sensorimotor cortex mouth and R IFG. He now showed a significant increase in activation in the L SMA compared to pre-TMS and at 3 mo. post-TMS (p < .02; p < .05, respectively). At 16 mo. there was also greater activation in L than R SMA (p < .08). At 46 mo. post-TMS (42% named), this new LH pattern of activation continued. He improved on the Boston Naming Test from 11 pictures named pre-TMS, to scores ranging from 14 to 18 pictures, post-TMS (2–43 mo. post-TMS). His longest phrase length (Cookie Theft picture) improved from three words pre-TMS, to 5–6 words post-TMS.Pre-TMS (1.5 years poststroke), P2 had significant activation in R IFG (3% pictures named). At 3 and 6 mo. post-TMS, there was no longer significant activation in R IFG, but significant activation was present in R sensorimotor cortex. On all three fMRI scans, P2 had significant activation in both the L and R SMA. There was no new, lasting perilesional LH activation across sessions for this patient. Over time, there was little or no change in his activation. His naming remained only at 1–2 pictures during all three fMRI scans. His BNT score and longest phrase length remained at one word, post-TMS.Lesion site may play a role in each patient’s fMRI activation pattern and response to TMS treatment. P2, the poor responder, had an atypical frontal lesion in the L motor and premotor cortex that extended high, near brain vertex, with deep white matter lesion near L SMA. P2 also had frontal lesion in the posterior middle frontal gyrus, an area important for naming (Duffau et al., 2003); P1 did not. Additionally, P2 had lesion inferior and posterior to Wernicke’s area, in parts of BA 21 and 37, whereas P1 did not.The fMRI data of our patient who had good response following TMS support the notion that restoration of the LH language network is linked in part, to better recovery of naming and phrase length in nonfluent aphasia.     

Within-session changes in responding during concurrent schedules with different reinforcers in the components.

Rats and pigeons responded on several concurrent schedules that provided different reinforcers in the two components (food and water for rats, Experiment 1; wheat and mixed grain for pigeons, Experiment 2). The rate of responding and the time spent responding on each component usually changed within the session. The within-session changes in response rates and time spent responding usually followed different patterns for the two components of a concurrent schedule. For most subjects, the bias and sensitivity to reinforcement parameters of the generalized matching law, as well as the percentage of the variance accounted for, decreased within the session. Negative sensitivity parameters were sometimes found late in the session for the concurrent food-water schedules. These results imply that within-session changes in responding could cause problems for assessing the validity of quantitative theories of concurrent-schedule responding when the components provide different reinforcers. They question changes in a general motivational state, such as arousal, as a complete explanation for within-session changes in responding. The results are compatible with satiation for, or sensitization-habituation to, the reinforcers as explanations.     

The Importance of Overt Responding in Programmed Instruction Even with Added Incentives for Learning

Among the fundamental tenets of programmed instruction is the requirement of overt responding. Past research has not determined when this tenet holds true. We systematically replicated the work of Tudor (1995) by showing that overt responding in computer-based instruction improves learning, even when there is an incentive that might be thought to improve learning enough to mask the effect of overt responding. Subjects were exposed to both read-only and overt-response materials. One group received course-related, bonus points based on posttest performance, whereas the other group received points simply for participation. Within-subject comparison showed greater performance increases when overt responding was required, regardless of the point incentive. No significant differences were found between groups.     

Ratio responding as a function of concurrent avoidance schedules, yoked shocks, and ratio value

Fixed-ratio food-reinforced responding in rats was studied alone and with concurrent shock avoidance or with concurrent response-independent shocks matched to those that occurred in the avoidance condition. Under each condition, fixed-ratio size was increased over successive daily sessions. Fixed-ratio response rate generally passed through a maximum as a function of fixed-ratio size. Decreased fixed-ratio responding at values beyond the maximum occurred when (1) the time to complete a fixed ratio approximated the response-shock interval of the avoidance schedule, (2) the shock rate increased, and/or (3) the ratio requirements were so high that ratio strain occurred. Avoidance rates decreased slightly as fixed-ratio size increased.