Transfer and Counterconditioning of Conditional Control in the Rabbit Nictitating Membrane Response

Two experiments using the rabbit nictitating membrane response investigated whether training in one conditional discrimination (A X+, B X-), enabled the feature cues (A and B) to modulate responding to another CS (Y) trained as a target stimulus in a second conditional discrimination (C Y+, D Y-). There was near-complete transfer of the feature cue's conditional control, indicating that the feature cue's ability to modulate responding is not based on an association specific to the training target. Experiment 2 also revealed that the role of a stimulus to act as a conditional cue is affected by its ability to act as a simple conditioned excitor or inhibitor. Following initial acquisition of two conditional discriminations, two feature cues were reinforced in a pattern consistent with the initial conditional discrimination (A +, B-), whereas the other two feature cues were reinforced in the reverse pattern to that of the original conditional discrimination (C-, D +). Subsequent tests revealed that the reversed training of the feature cues interfered with the original conditional discriminations. The results are consistent with theories that the feature cue gains an association with a representation of the emotional attributes of the US, which acts to modulate responding to the target stimulus through a diffuse change in motivational level. However, hierarchical theories of conditional discriminations that assume a lack of CS-specificity may also be able to explain the findings.     

Pavlovian counterconditioning: changing the suppressive properties of shock by association with food.

Two experiments are described in which rats received a series of shock and food presentations in a Pavlovian counterconditioning sequence. Subsequently, the capacity of the shock to act as a reinforcer during conditioned emotional response (CER) training was assessed. In the first experiment, following each shock during counterconditioning by a food presentation was found to retard the development of suppression during CER training relative to control conditions in which different groups of rats received either a sequence of explicitly unpaired shock and food presentations, shock presentations alone, or food presentations alone. The second experiment demonstrated that when the magnitude of the food presentations is held constant, the attenuation of the suppressive properties of shock by pairing with food depends on the magnitude of the shock. The results are interpreted as demonstrations of Pavlovian counterconditioning, which, it is suggested, modifies the general aversiveness of a noxious stimulus.     

Transfer of control in ambiguous discriminations

Rats' acquisition and transfer of performance in ambiguous discriminations was examined using discrete-trial operant lever-press procedures. Rats learned serial ambiguous discriminations (X----A+, A-; B+, X----B-) by acquiring both positive and negative occasion setting functions to the X feature. Mutual transfer occurred among cues from serial ambiguous, feature positive (Y----C+, C-), and feature negative (Y----C-, C+) discriminations, but that transfer did not extend to cues not trained within one of those serial discriminations. The ambiguous feature's positive occasion setting powers were unaffected by nonreinforced presentation of that feature alone, and posttraining counterconditioning did not eliminate the feature's ability to serve as a negative occasion setter. Occasion setting was not acquired with simultaneous ambiguous discriminations (XA+, A-; XB-, B+), which apparently were solved with a configural strategy.     

Determining whether attentional control settings are inclusive or exclusive

The aim of the present study was to determine whether attentional control settings operate with an inclusive rule (orient attention to stimuli that share a task-relevant feature with the target) or an exclusive rule (do not orient attention to stimuli that do not share a task-relevant feature with the target). All three experiments used a variation of the Folk and Remington (e.g., Folk, Remington, & Johnston, 1992) paradigm. In Experiment 1, cuing effects were found for combination cues (cues containing an onset feature and a color feature) with both onset and color targets. Experiment 2, using a delay between cue and target, revealed inhibition of return (IOR) for combination cues with onset and color targets. Unexpectedly, IOR was also found for onset cues with color targets, and this finding was confirmed in Experiment 3. These findings indicate that attentional control settings use an inclusive rule. Moreover, the presence of IOR with onset cues and color targets suggests that onset cues may automatically capture attention, but attention control settings allow for rapid disengagement when the onset cue does not contain a task-relevant feature.     

Environment size and the use of feature and geometric cues for reorientation

We tested associative-based accounts of orientation by investigating the influence of environment size on the use of feature and geometric cues for reorientation. Two groups of participants were trained in dynamic three-dimensional virtual rectangular environments that differed in size to find a distinctly colored bin located at one of the four corners. Subsequently, we probed the reliance on feature and geometric cues for reorientation during test trials by presenting six trial types: Small Geometry Only, Large Geometry Only, Small Cue Conflict, Large Cue Conflict, Small Distal, and Large Distal. During Geometry Only test trials, all bins were black; thus, all distinctive featural information was removed leaving only geometric cues. For Cue Conflict test trials, all colored bins were shifted counter-clockwise one corner; thus, the geometric cues from the trained corner and the trained color were in direct conflict. During Distal test trials, the bin in the geometrically incorrect corner farthest from the trained corner was colored the same as during training; the remaining three bins were black. Thus, only this distant feature cue could be used to determine the location of the goal bin. Results suggested that geometric cues were used across changes in environment size, featural cues exerted greater influence when in conflict with geometric cues, and the far featural cue was used to disambiguate the correct from the rotationally equivalent location. In short, both feature and geometric cues were used for reorientation, and environment size influenced the relative use of feature and geometric cues. Collectively, our results provide evidence against associative-based accounts of orientation.     

Bonobos, chimpanzees, gorillas, and orang utans use feature and spatial cues in two spatial memory tasks

Animals commonly use feature and spatial strategies when remembering places of interest such as food sources or hiding places. We conducted three experiments with great apes to investigate strategy preferences and factors that may shape them. In the first experiment, we trained 17 apes to remember 12 different food locations on the floor of their sleeping room. The 12 food locations were associated with one feature cue, so that feature and spatial cues were confounded. In a single test session, we brought the cues into conflict and found that apes, irrespective of species, showed a preference for a feature strategy. In the second experiment, we used a similar procedure and trained 25 apes to remember one food location on a platform in front of them. On average, apes preferred to use a feature strategy but some individuals relied on a spatial strategy. In the final experiment, we investigated whether training might influence strategy preferences. We tested 21 apes in the platform set-up and found that apes used both, feature and spatial strategies irrespective of training. We conclude that apes can use feature and spatial strategies to remember the location of hidden food items, but that task demands (e.g. different numbers of search locations) can influence strategy preferences. We found no evidence, however, for the role of training in shaping these preferences.     

Use of position and feature cues in discrimination learning by the whiptail lizard (Cnemidophorus inornatus)

Animals use a variety of cue types to locate and discriminate objects. The ease with which particular cue types are learned varies across species and context. An enormous literature contains comparisons of spatial cue use to use of other cue types, but few experiments examine the ease with which various nonspatial cues are learned. In addition, few studies have examined cue use in reptiles. Thus, the authors compared whiptail lizards' (Cnemidophorus inornatus) ability to learn and reverse a discrimination using either position (left or right) or visual feature cues. Lizards learned and reversed the task using position cues faster and with greater accuracy than using feature cues.     

Some effects of acoustic attributes of speech on the processing of phonetic feature information

How do acoustic attributes of the speech signal contribute to feature-processing interactions that occur in phonetic classification? In a series of five experiments addressed to this question, listeners performed speeded classification tasks that explicitly required a phonetic decision for each response. Stimuli were natural consonant-vowel syllables differing by multiple phonetic features, although classification responses were based on a single target feature. In control tasks, no variations in nontarget features occurred, whereas in orthogonal tasks nonrelevant feature variations occurred but had to be ignored. Comparison of classification times demonstrated that feature information may either be processed separately as independent cues for each feature or as a single integral segment that jointly specifies several features. The observed form on processing depended on the acoustic manifestations of feature variation in the signal. Stop-consonant place of articulation and voicing cues, conveyed independently by the pattern and excitation source of the initial formant transitions, may be processed separately. However, information for consonant place of articulation and vowel quality, features that interactively affect the shape of initial formant transitions, are processed as an integral segment. Articulatory correlates of each type of processing are discussed in terms of the distinction between source features that vary discretely in speech production and resonance features that can change smoothly and continuously. Implications for perceptual models that include initial segmentation of an input utterance into a phonetic feature representation are also considered.     

Training attention: Interactions between central cues and reflexive attention

Three experiments are reported in which we investigate whether the recently reported interactions between central cues (e.g., arrows) and reflexive attention are attributable to the overlearned spatial properties of certain central cues. In all three experiments, a nonpredictive cue with arbitrary spatial properties (a colour patch) is presented prior to a detection target in the left or right visual field. Reaction times to detect targets are compared before and after a training session in which participants are trained to associate each colour patch with left and right space, either via a target detection task in which colour predicts target location 100% of the time (Experiments 1 and 3), or via a left/right motor movement as a function of colour (Experiments 2 and 3). In the first two experiments, a small but highly significant training effect is observed. Participants are approximately 10 ms faster to detect targets at congruent locations relative to incongruent locations after training relative to before training, despite the fact that cue colour was nonpredictive during the test sessions. In Experiment 3, the length of the training session is increased and the magnitude of the training effect also increases as a result. Implications for the interaction between central cues and reflexive attention, as well as premotor theory of attention, are discussed.     

Counterconditioning of appetitive and defensive CRs in rabbits

Two experiments examined interactions between conditioned appetitive and defensive responses in the rabbit. In Experiment I, a conditioned jaw-movement response was established by following presentations of a clicker CS with intra-oral sucrose delivery on 50% of trials. The jaw-movement response was then maintained on this partial reinforcement schedule during a counterconditioning phase. A group which received para-orbital shock paired with the CS on non-sucrose trials showed acquisition of eyeblink responding and suppression of jaw-movement responding to the CS, in comparison to control groups which received either no shock or unpaired presentations of the CS and shock. Experiment II was identical in design to Experiment I except that the roles of the sucrose and shock reinforcers were reversed. The paired group acquired a conditioned jaw-movement response when sucrose was added in the counterconditioning phase, but in contrast to Experiment I showed a slight enhancement of the previously established eyeblink response. The asymmetry of appetitive and defensive counterconditioning was discussed in relation to opponent-process theories of motivation and reinforcement.     

Extinction in human learning and memory

In two experiments, participants were given extinction training in a human causal learning task. In both experiments, three critical experimental cues were paired with different outcomes in a first phase of training and were then extinguished in a second phase. Three control cues were given the same treatment in the first phase of training, but were not then presented in the second phase. Participants' ability to correctly identify the outcome with which each cue had been paired in the first phase was lower for extinguished than for control cues. Causal attributions to the extinguished cues were also lower than those to the control cues, a difference that correlated with outcome memory. These data are consistent with the idea that extinction in causal judgement is due, at least in part, to a failure to remember the cue–outcome relationship encoded in the first phase of training.     

Extinction in human learning and memory

In two experiments, participants were given extinction training in a human causal learning task. In both experiments, three critical experimental cues were paired with different outcomes in a first phase of training and were then extinguished in a second phase. Three control cues were given the same treatment in the first phase of training, but were not then presented in the second phase. Participants' ability to correctly identify the outcome with which each cue had been paired in the first phase was lower for extinguished than for control cues. Causal attributions to the extinguished cues were also lower than those to the control cues, a difference that correlated with outcome memory. These data are consistent with the idea that extinction in causal judgement is due, at least in part, to a failure to remember the cue-outcome relationship encoded in the first phase of training.     

Spatial updating and training effects in the first year of human infancy

The ability of infants to locate an invisible target after reorientation in their direction of facing was examined in a series of experiments. In a featureless environment, localization of the target site improved between 4 and 8 months. At 8 months it was shown to be dependent on the training procedure. Infants received either instrumental training in which they were trained to anticipate the occurrence of an event at the site, or association training in which one event immediately followed another regardless of their responses. After instrumental training, localization was dependent on visual cues whereas after association training it occurred whether or not visual cues were provided. Contrary to earlier findings, it was concluded that an updating strategy based on proprioceptive information is operative from the second half of the first year.     

Pavlovian counterconditioning is unchanged by chlordiazepoxide or by septal lesions

Two experiments were performed to test whether the minor tranquillizer chlordiaz-epoxide or septal lesions could interfere with Pavlovian counterconditioning. Rats were first trained to bar-press for food on a random interval schedule on which was superimposed the presentation of a light which predicted delivery of a shock. This training continued until all animals were showing stable suppression of responding to the light. Separate groups were then presented, while the manipulandum was retracted from the box, with either a shock paired with the delivery of food or shock and food delivery in a random relationship with one another. This type of intrusion period alternated with the presentation of the light and shock. Pavlovian counterconditioning developed, as shown by progressively less response suppression in the paired groups compared to the random groups. This Pavlovian counterconditioning was in no way reduced by either chlordiazepoxide (5 mg/kg) or by medial or lateral septal lesions. It is argued that these results rule out Pavlovian counterconditioning as a process which is affected by minor tranquillizers or by septal lesions when they interfere with the behavioural tolerance observed after partial punishment or partial reward schedules.     

Role of endpoints and closures in feature search1

Abstract: The present study intended to examine the role of endpoints and of closures, the two most frequently referred to features, in a feature‐search paradigm. Two experiments were conducted with a rigorous stimulus control using random lined figures of different levels of complexity. The experiments gave almost identical results: there was no search asymmetry between the two features, smaller latencies were obtained in the presence of a feature as a target rather than in its absence, and the latencies were smaller for the displays having a background consisting of closures rather than for those having a background of endpoints. The results were more comprehensively explained by the high contrast between an endpoint as a target and closures as a background, rather than the conspicuity of an endpoint as a target. The possibility for closures to group into a homogeneous ground was discussed.     

Allocating attention in the visual field: the effects of cue type and target-distractor confusability

In the present study I compared the effect of colour and location cues on the selection of a target. Two questions were in focus. First, can both colour and location cues trigger and mediate attentional selection, and if they can, which of them is more effective? Second, does physical distinctiveness between a target and a distractor have to be taken into account? In two experiments, in which the most likely target colour or location was cued, both colour cues and arrow-like location cues produced cue-validity effects. The relative effectiveness of feature cues and location cues appeared, to some extent, to be dependent on target-distractor confusability. Taken together, the results support the post-categorical filter theory, in which different cues can be used to trigger the feedback loop that is used to address relevant identity information via location.     

Visual search for singleton feature targets within and across feature dimensions

Three experiments investigated visual search for singleton feature targets. The critical dimension on which the target differed from the nontargets was either known in advance or unknown—that is, the critical difference varied eitherwithin a dimension oracross dimensions. Previous work (Treisman, 1988) had shown that, while the search reaction time (RT) functions were flat in both conditions, there was an intercept cost for the cross-dimension condition. Experiment 1 examined whether this cost would disappear when responses could be based on the detection ofany (target—nontarget) difference in the display (by requiring a “heterogeneity/homogeneity” decision). The cost remained. This argues that pop-out requires (or involves) knowledge of the particular dimension in which an odd-one-out target differs from the nontargets; furthermore, that knowledge is acquired through the elimination of dimensions not containing a target. In Experiment 2, the subjects had to eliminate (or ignore) one potential source of difference in order to give a positive response (displays could contain a “noncritical” difference requiring a negative response). The result was a comparatively large cost in the within-dimension (positive) condition. This can be taken to indicate that popout as such does not make available information as to the particular feature value in which the target differs from the nontargets. Experiment 3 examined whether search priorities can be biased in accordance with advance knowledge of the likely source of difference. The subjects were found to have a high degree of top-down control over what particular dimension to assign priority of checking to. The implication of the results for models of visual search and selection are discussed.     

The relationship between discrimination and memory for spacing and feature changes in houses

Adults need to discriminate between stimuli and recognize those previously seen. For faces, feature changes (e.g., different eyes) and spacing changes (e.g., distances between eyes) are important cues. In two experiments, we assessed the influence of these on discrimination and recognition of houses, a commonly used control in face studies. In both experiments, discrimination was better for feature than spacing changes. Memory for spacing changes was generally poor but aided by extra learning and intermixing change types. Conversely, memory for features was good, especially when there were few houses, and change type was blocked. Unexpectedly, memory was best for differences that might signal something about occupants (e.g., changes to garden or bins), perhaps akin to hairstyles for faces. Overall, results are consistent with previous work showing poor discrimination of spacing in non-face objects and extends them to show that, unlike for faces, spacing differences are also not well remembered.     

The effects of feature type in operant serial feature-positive discriminations

In two experiments, rats were trained on two operant serial feature positive discriminations in which one feature was a flavored solution and the second feature was a visual or auditory cue. As in a previous study ([Goddard and Holland, 1996]), transfer of a feature’s control to the target of the other discrimination was not observed when the flavor feature and the reinforcer were flavored sucrose solutions (Experiment 1). The performance of comparison groups showed that this lack of transfer was not due to confounded differences in the event contingencies resulting from having similar stimuli serve as feature and reinforcer. By contrast, in Experiment 2, transfer was observed between visual and flavor features when the flavor feature was unsweetened and the reinforcer was plain sucrose. These results suggest that the lack of transfer in Experiment 1 and in [Goddard and Holland, 1996] study were related to the biological significance or hedonic properties of the sucrose feature.     

The development of induction based on noun and feature labels

In two experiments, we examined the development of sensitivity to the inductive potential of shared novel noun and feature labels. Children (4-year-olds, 5-year-olds, and 8-year-olds) and adults were presented with a complete base stimulus and an incomplete target. The task was to infer whether the missing target feature matched the corresponding base feature. The base and target were given matching or mismatching novel labels, which were either count nouns or adjectives describing object features. Use of matching labels for induction increased with age. Nevertheless, all age groups were more likely to make inferences based on novel noun labels rather than feature labels. These results support the view that even preschool children grasp the conceptual significance of count nouns for induction.