Stimulus control of responding during a fixed-interval reinforcement schedule

During training sessions, pecks by pigeons on a response key illuminated by a vertical line of white light resulted in reinforcement and an ensuing blackout according to a fixed-interval schedule. Training sessions were followed by dimensional stimulus control test sessions during which the orientation of the line present throughout the fixed interval was varied. Inverted U-shaped (excitatory) gradients of responding, with maximum responding occurring in the presence of the vertical line, were observed during the terminal part of the fixed interval. U-shaped (inhibitory) gradients of responding, with minimum responding occurring in the presence of the vertical line, were observed during the early part of the fixed interval when the preceding interval had terminated with reinforcement and blackout but not when the preceding interval had terminated with blackout only. These results suggest that the dimensional control by the stimulus present throughout the fixed interval is of a conditional variety. Whether the fixed-interval stimulus exerts inhibitory or excitatory dimensional control depends upon the presence and absence, respectively, of stimuli associated with reinforcement.     

Circling a memory: a layered reflective method for generating subjective knowledge about childhood and teacher identity

This paper describes a memory and life story process engaged in by three former early childhood teachers. The reflective process was based in interpretative phenomenological analysis (IPA) and proceeded in a recursive and layered manner, circling around the participants’ memory narratives. The aims of the study were: (1) to develop a critical approach to generating knowledge about childhood, and (2) to consider a teaching strategy for memory work in teacher education programs.     

Gerbils in space: performance on the 17-arm radial maze.

In Experiment 1 six hungry gerbils received six trials per day on a 17-arm radial maze. During each trial the subjects were allowed to choose freely among the arms, each of which contained a food pellet, until each arm had been visited once or until eight minutes had elapsed. An error was recorded when the subject entered a previously visited arm. The gerbils quickly learned not to re-enter previously visited arms and generally made errors on fewer than 15% of entries, performance comparable to that of the rat and superior to that of other species tested in the radial arm maze. The intertrial-interval duration did not affect accuracy of arm choices during acquisition but did influence asymptotic accuracy. Accuracy did not change systematically over the six trials. A high proportion of arm entries were to nearby arms. Errors occurred most often towards the end of a trial. Odor cues were not important. When the number of trials per day was reduced from six to one, accuracy deteriorated slightly. In Experiment 2 neither the transposition of extramaze cues nor the placement of the maze in a different room had large disruptive effects on accuracy. In Experiment 3 the addition of three explicit intramaze brightness cues aided accuracy, perhaps by permitting the subjects to decompose the large maze into three smaller mazes, although there was no direct evidence that this was the case. Implications of a number of these results for models of spatial maze performance were discussed.     

Errorless discrimination established by differential autoshaping

In Experiment I, pigeons exposed to a differential autoshaping procedure pecked a key in the presence of the stimulus associated with reinforcement but did not peck, or pecked infrequently, in the presence of the stimulus associated with nonreinforcement. In Experiment II, pigeons were exposed to a differential autoshaping procedure in which one stimulus was associated with reinforcement and two stimuli were associated with nonreinforcement. The birds initially responded in the presence of one stimulus associated with nonreinforcement but never responded in the presence of the second stimulus associated with nonreinforcement. They were subsequently exposed to an autoshaping procedure in which reinforcement followed both these stimuli. The number of stimulus-reinforcement pairings required to establish pecking in the presence of the stimulus during which responses had not previously occurred suggested that such stimuli are inhibitory. These findings have implications for autoshaping, errorless discrimination, inhibition, and theories of discrimination byproducts.     

Attention in the pigeon: a reevaluation

During training sessions, pigeons were successively exposed to compounds consisting of a white triangle on a red background and a white circle on a green background. Key pecking intermittently produced grain reinforcers in the presence of one form-color compound. Once key pecking was confined to the compound associated with reinforcement, the elements—red, green, triangle, and circle—were presented during a test in which no reinforcement was available. Each bird pecked nearly exclusively in the presence of the color previously associated with reinforcement, a result that might be interpreted as indicating that the subjects had attended to color, but not form during training. Pecking was next reinforced when either the triangle or the circle was present. Pecking in the presence of the form previously associated with reinforcement was acquired more rapidly. This result suggests that the birds had learned about the forms during training, and that conclusions about attention based on the lack of differential pecking in the nonreinforcement test may not be appropriate.     

Contrast and induction in rats on multiple schedules

Eight rats were trained on a variable-interval schedule in the presence of a light (Phase I). Responding was then extinguished in the presence of darkness that alternated with the light (Phase II). Reinforcement was then introduced in the presence of darkness (Phase III). Several rats were then returned to the condition of Phase II (Phase IV) and then to that of Phase III (Phase V). The responding of most rats showed clear behavioral contrast in Phase II—i.e., an increase in responding in the presence of the light. When, for three rats, Phase III was introduced early after the occurrence of positive contrast, either positive induction occurred, i.e., an increase in responding in the presence of the light, or there was little change. Negative contrast did not occur. It was further shown that positive contrast dissipates over time, thus replicating a result previously obtained with pigeons and that the positive induction effect seems also to dissipate over time. The introduction of reinforcement in the presence of darkness (Phases III and V) after the dissipation of positive contrast seemed to have little consistent effect.     

Delayed reinforcement in a multiple schedule

Three rats and a pigeon were first trained on a two-component multiple schedule in which reinforcement in the two components occurred immediately after a response. Later, reinforcement in one component was delayed by a few seconds. During both stages of the experiment, reinforcement was scheduled by equal variable- (pigeon) or random-interval (rats) schedules in the two components. The main effect of the delayed reinforcement was to increase the rate of responding in the unchanged (non-delay) component. This behavioral contrast effect did not appear in all cases to be dependent upon a reduction in the rate of responding or the frequency of reinforcement in the delay component. This finding suggests that a reduction in response rate and/or reinforcement frequency in one component of a multiple schedule may not be a necessary prerequisite for the occurrence of behavioral contrast. This finding is, however, consistent with an explanation that suggests that behavioral contrast results from the introduction of a less-preferred condition in one component of a multiple schedule, since it is known that animals “prefer” immediate to delayed reinforcement.     

A partial matching theory of the mirror effect in immediate probed recognition

A set of experiments on immediate probed recognition of digit triples is reported in which the variables were list length (five, six, seven, or eight triples), the probability that a probe was old (.33, .5, or .67), and whether the digit triples were presented with an auditory component or articulatory suppression. Previous work had suggested that the false alarm (FA) rate in this paradigm was lower when auditory information was available than when it was not; this observation had led to the development of thepartial matching theory of immediate probed recognition, according to which FAs could arise not only as a result of unlucky guesses but also when new probes shared a first digit in common with a partially retained target triple. It was argued that partial memory representations were less likely following auditory presentation than following articulatory suppression. Partial matching theory is contrasted with therational response theory, according to which all FAs are unlucky guesses; partial matching theory gave a better account of the present experimental data than did rational response theory. However, a logical relationship between the two theories was suggested, a consequence of which was that rational response theory could be modified to include partial matching in such a way as to account for mirror effects, not only in unusually difficult immediate probed recognition tasks, but also in the more commonly studied mixed test list paradigm involving words of high or low frequency.     

The occurrence of different intrusive errors in patients with Alzheimer's disease, multiple cerebral infarctions, and major depression.

Recent evidence suggests that specific types of intrusive errors may occur more often in the protocols of Alzheimer's disease (AD) patients than in those of patients diagnosed with other types of dementia. Using the FULD Object Memory Evaluation, we documented the occurrence of five qualitatively different types of intrusive errors for mildly and moderately impaired patients with AD and multiple cerebral infarctions (MCI). Depressed and normal elderly controls were also studied. Despite an equivalent degree of impairment on a broad array of neuropsychological measures, mildly impaired AD patients evidenced greater deficits on a measure tapping retrieval from semantic memory and demonstrated a higher occurrence of specific types of intrusive errors relative to their mildly impaired MCI counterparts. Further, both of these measures were highly correlated, suggesting that these indices may be particularly sensitive to semantic dysfunction associated with early AD.     

Pain tolerance selectively increased by a sweet-smelling odor

The mechanism underlying reported analgesic effects of odors in humans is unclear, although odor hedonics has been implicated. We tested whether odors that are sweet smelling through prior association with tasted sweetness might influence pain by activating the same analgesic mechanisms as sweet tastes. Inhalation of a sweet-smelling odor during a cold-pressor test increased tolerance for pain compared with inhalation of pleasant and unpleasant low-sweetness odors and no odor. There were no significant differences in pain ratings among the odor conditions. These results suggest that smelled sweetness can produce a naturally occurring conditioned increase in pain tolerance.