Auditory spatial concepts in blind football experts

ObjectivesWe compared the spatial concepts given to sounds' directions by blind football players with both blind non-athletes and sighted individuals.MethodParticipants verbally described the directions of sounds around them by using predefined spatial concept labels, under two blocked conditions: 1) facing front, 2) pointing with the hand towards the stimulus.ResultsBlind football players categorized the directions more precisely (i.e., they used simple labels for describing the cardinal directions and combined labels for the intermediate ones) than the other groups, and their categorization was less sensitive to the response conditions than blind non-athletes. Sighted participants' categorization was similar to previous studies, in which the front and back regions were generally more precisely described than the sides, where simple labels were often used for describing directions around the absolute left and right.ConclusionsThe differences in conceptual categorization of sound directions are a) in sighted individuals, influenced by the representation of the visual space b) in blind individuals, influenced by the level of expertise in action and locomotion based on non-visual information, which can be increased by auditive stimulation provided by blind football training.     

Cognitive representation of auditory space in blind football experts

ObjectivesWe compared the mental representation of sound directions in blind football players, blind non-athletes and sighted individuals.DesignStanding blindfolded in the middle of a circle with 16 loudspeakers, participants judged whether the directions of two subsequently presented sounds were similar or not.MethodStructure dimensional analysis (SDA) was applied to reveal mean cluster solutions for the groups.ResultsHierarchical cluster analysis via SDA resulted in distinct representation structures of sound directions. The blind football players' mean cluster solution consisted of pairs of neighboring directions. The blind non-athletes also clustered the directions in pairs, but included non-adjacent directions. In the sighted participants' structure, frontal directions were clustered pairwise, the absolute back was singled out, and the side regions accounted for more directions.ConclusionsOur results suggest that the mental representation of egocentric auditory space is influenced by sight and by the level of expertise in auditory-based orientation and navigation.     

Control of responding by sound location in monkeys: rapid acquisition in darkness.

Rapid control of responding by sound location is obtained in squirrel monkeys when sound stimuli are presented from one of two loudspeakers, each one adjacent to a response key. With this arrangement of loudspeakers and response keys, squirrel monkeys quickly learn to respond on the key near the source of the sound stimulus, and this pattern is the same whether or not responses near the sound source are differentially reinforcedmthis result may depend on a pre-experimental tendency in squirrel monkeys to orient head and eyes toward a sound, which would lead the animal to look at the response key in front of the loudspeaker producing the sound. The present experiment sought to determine whether visual stimuli are necessary for rapid control of responding by sound location. Two monkeys were trained in darkness in a sound-localization task similar to that described above. Results were similar to those obtained from animals trained in light, indicating that visual stimuli are not required for rapid acquisition of sound-localization behavior in monkeys.     

Does ignoring lead to worse evaluations? A new explanation of the stimulus devaluation effect

Affective evaluation of stimuli just seen in visual search tasks has been shown to depend on task-relevant stimulus configuration (Raymond, Fenske, & Tavassoli, 2003): Whereas targets and novel stimuli were evaluated similarly, distractors were devaluated. These results were explained by an inhibition-based account of the influence of selective attention on emotion. In the present experiments, we demonstrated that stimulus devaluation might not be a consequence of attentional inhibition. By simply instructing participants to react to an accepted or rejected stimulus in the visual search task of Experiment 1, we found distractor devaluation in the first case and target devaluation in the second case. We conclude that devaluation of stimuli is mediated by the affective connotation implied by response labels and instructions. This was confirmed in Experiment 2: To-be-ignored stimuli were not devaluated when participants knew that those stimuli would become task-relevant during the experiment.     

A comparison of displacement and reinforcer potency for typically developing children

Previous researchers found that individuals with intellectual and developmental disabilities tend to prefer edible over leisure stimuli, although leisure stimuli may still function as reinforcers. We replicated and extended previous research in a 2-part experiment with typically developing children. In Experiment 1, we evaluated 15 children's preference for leisure and edible stimuli. Five of 15 participants preferred edible over leisure stimuli, 3 of 15 participants preferred leisure over edible stimuli, and the remaining 7 of 15 participants did not show a preference for a stimulus class. In Experiment 2, we compared the reinforcer potency of the top-ranked stimulus from each class with 7 of the 8 participants who showed displacement of one stimulus class. Four of 7 participants allocated more responding to the task associated with the top-ranked stimulus and 3 of 7 participants showed no differences in responding to the task regardless of the stimulus rank.     

Task-irrelevant sounds influence both temporal order and apparent-motion judgments about tactile stimuli applied to crossed and uncrossed hands

It has been suggested that judgments about the temporal–spatial order of successive tactile stimuli depend on the perceived direction of apparent motion between them. Here we manipulated tactile apparent-motion percepts by presenting a brief, task-irrelevant auditory stimulus temporally in-between pairs of tactile stimuli. The tactile stimuli were applied one to each hand, with varying stimulus onset asynchronies (SOAs). Participants reported the location of the first stimulus (temporal order judgments: TOJs) while adopting both crossed and uncrossed hand postures, so we could scrutinize skin-based, anatomical, and external reference frames. With crossed hands, the sound improved TOJ performance at short (≤300 ms) and at long (>300 ms) SOAs. When the hands were uncrossed, the sound induced a decrease in TOJ performance, but only at short SOAs. A second experiment confirmed that the auditory stimulus indeed modulated tactile apparent motion perception under these conditions. Perceived apparent motion directions were more ambiguous with crossed than with uncrossed hands, probably indicating competing spatial codes in the crossed posture. However, irrespective of posture, the additional sound tended to impair potentially anatomically coded motion direction discrimination at a short SOA of 80 ms, but it significantly enhanced externally coded apparent motion perception at a long SOA of 500 ms. Anatomically coded motion signals imply incorrect TOJ responses with crossed hands, but correct responses when the hands are uncrossed; externally coded motion signals always point toward the correct TOJ response. Thus, taken together, these results suggest that apparent-motion signals are likely taken into account when tactile temporal–spatial information is reconstructed.

     

Novelty and frequency as determinants of newborn preference

The debate over whether infants prefer a familiar stimulus over a novel stimulus has persisted for over 30 years, and there is evidence which supports both sides of the question. However, the research which supports the preference for the familiar uses different measures than that which supports the preference for novelty. In the first experiment, the preference for the familiar was tested by making one stimulus more familiar than the others presented. A target of a ‘familiar’ face was presented eight times more frequently than the other faces. During the experiment, the infants could choose at which face they looked and for how long. It was found that the infants significantly preferred the familiar face over any one of the novel faces, especially when the familiar face was presented first. Substituting auditory for visual stimuli, the second experiment was a replication of the first experiment. Consonant–vowel syllables were used instead of faces. Overall, 17 stimuli were used: one repeating ‘familiar’ sound, and 16 novel sounds. It was found that the infants significantly preferred the familiar sound over any of the novel sounds. As found in Experiment 1, the infants also had a greater preference for the familiar sound when it was presented first.     

Two operations in character recognition: Some evidence from reaction-time measurements

Theories of the recognition of a visual character may be divided into three sets.defined by the way in which the stimulus is encoded before being compared to a memorized target character. A character-classification experiment was performed in which the test stimuli were characters that were either intact or degraded by a superimposed pattern. Analyses of reaction-times in the experiment lead to the rejection of two of the three sets of theories. There appear to be at least two separate operations in the recognition or classification of a character. The first encodes the visual stimulus as an abstracted representation of its physical properties. The second, which may occur more than once, compares such a stimulus representation to a memory representation, producing either a match or a mismatch. A theory of high-speed exhaustive scanning in memory underlies the experiment and is given new support. The method of reaction-time analysis that is introduced, an elaboration of the Uelmholtz-Donders subtraction method, may be applicable to the general problem of the invariance ofperceived form under certain transfomations of the stimulus.     

Electrophysiological evidence for a shared representational medium for visual images and visual percepts

Does mental imagery involve the activation of representations in the visual system? Systematic effects of imagery on visual signal detection performance have been used to argue that imagery and the perceptual processing of stimuli interact at some common locus of activity (Farah, 1985). However, such a result is neutral with respect to the question of whether the interaction occurs during modality-specific visual processing of the stimulus. If imagery affects stimulus processing at early, modality-specific stages of stimulus representation, this implies that the shared stimulus representations are visual, whereas if imagery affects stimulus processing only at later, amodal stages of stimulus representation, this implies that imagery involves more abstract, postvisual stimulus representations. To distinguish between these two possibilities, we repeated the earlier imagery-perception interaction experiment while recording event-related potentials (ERPs) to stimuli from 16 scalp electrodes. By observing the time course and scalp distribution of the effect of imagery on the ERP to stimuli, we can put constraints on the locus of the shared representations for imagery and perception. An effect of imagery was seen within 200 ms following stimulus presentation, at the latency of the first negative component of the visual ERP, localized at the occipital and posterior temporal regions of the scalp, that is, directly over visual cortex. This finding provides support for the claim that mental images interact with percepts in the visual system proper and hence that mental images are themselves visual representations.     

Relative and Absolute Judgments of Speech Rate from Masked and Content-Standard Stimuli The Influence of Vocal Frequency and Intensity

In two previous studies, the perception of speech rate was found to be positively related to the vocal frequency and intensity of speech. In those studies, a single sample of spontaneous, content-masked speech was used to produce nine stimuli by factorially varying three levels of each vocal frequency and intensity, while controlling the actual speech rate of the stimuli. Participants were asked to judge each stimulus, preceded by a standard, “anchoring,” stimulus as to its speech rate, pitch, loudness, and duration. The purpose of the three studies reported here was to examine the generalizability of the previous findings by using stimuli that were nonmasked and/or were not preceded by an anchoring stimulus. In each study, nine speech stimuli were prepared, as described above, and participants were asked to make judgments about the rate, pitch, loudness, and duration of each stimulus. In the first study, the stimuli were masked but were not preceded by an anchoring stimulus. In the second study, participants listened to content-standard speech stimuli preceded by an anchoring stimulus. Finally, in the third study, content-standard stimuli without an anchoring stimulus were used. In addition, studies two and three used speech segments of a male and a female speaker. The findings from the three studies replicated the central findings of the previous studies. They suggest, in other words, that rate perception of speech is indeed influenced by vocal frequency and, to some extent, by intensity, and that these relationships are not materially altered by the speakers'gender.     

Visual factors in auditory localization

Previous experiments showing the importance of visual factors in auditory localization are shown to have been insufficiently quantitative.

In the first Experiment, bells were rung and lights shone on the same or different vectors, eleven subjects indicating which bell had rung. In the second Experiment, a puff of steam was seen to issue from a kettle whistle with no whistling sound, while similar whistles were sounded by compressed air on that or another vector. Twenty-one subjects cooperated.

The addition of a visual stimulus at 0° deviation increased the percentage of correct responses significantly in the second, and insignificantly in the first experiment. At 20°-30° deviation the proportion of naive responses to the visual cue was 43 per cent. in the first and 97 per cent, in the second experiment. At greater angular deviations, the proportion of naive responses fell to chance level in the first, but remained significant in the second experiment, even at 90°. The “visuo-auditory threshold” was found to be 20°-30°, but might be much larger if there were more grounds for supposing the two stimuli to be from the same source in space.     

Do chickens (Gallus gallus f. domestica) decompose visual figures?

To investigate whether learning to discriminate between visual compound stimuli depends on decomposing them into constituting features, hens were first trained to discriminate four features (red, green, horizontal, vertical) from two dimensions (colour, line orientation). After acquisition, hens were trained with compound stimuli made up from these dimensions in two ways: a separable (line on a coloured background) stimulus and an integral one (coloured line). This compound training included a reversal of reinforcement of only one of the two dimensions (half-reversal). After having achieved the compound stimulus discrimination, a second dimensional training identical to the first was performed. Finally, in the second compound training the other dimension was reversed. Two major results were found: (1) an interaction between the dimension reversed and the type of compound stimulus: in compound training with colour reversal, separable compound stimuli were discriminated worse than integral compounds and vice versa in compound training with line orientation reversed. (2) Performance in the second compound training was worse than in the first one. The first result points to a similar mode of processing for separable and integral compounds, whereas the second result shows that the whole stimulus is psychologically superior to its constituting features. Experiment 2 repeated experiment 1 using line orientation stimuli of reversed line and background brightness. Nevertheless, the results were similar to experiment 1. Results are discussed in the framework of a configural exemplar theory of discrimination that assumes the representation of the whole stimulus situation combined with transfer based on a measure of overall similarity.     

Identification asymmetry of parafoveal stimulus pairs

Three experiments, involving 8, 10, and 10 naive participants, respectively, were conducted to examine the phenomenon in which the peripheral member of a parafoveally appearing stimulus pair is more accurately identified than the central. In the first experiment, the asymmetry was observed with stimulus pairs which had but one distinguishing feature; this could have implications for the notion that feature perturbations between stimuli provide the basis for the effect. The second experiment eliminated an explanation based upon acuity at the position of the midpoint of the stimulus configuration, since the asymmetry remains when this position is held constant. The involvement of response or decision factors seems unlikely, since the third experiment found the effect with blocked presentations involving responses to only one member of the pair. It is concluded that accounts which appeal to difficulties in separating stimuli from the overall pair configuration fail to explain more accurate identification of the peripheral stimulus when the pair is positioned at a constant distance from fixation.     

Recognition memory for tactile sequences.

In three experiments participants were required to compare the similarity in item order for two temporally separated sequences of tactile stimuli presented to the fingers of the hand. Between-sequence articulatory suppression but not tactile interference impaired recognition accuracy (Experiment 1), and the null effect of tactile interference was not due to the second tactile sequence overwriting the sensory record of the first sequence (Experiment 2). Experiment 3 showed that compared to a condition where the second sequence was presented in the tactile modality only, recognition was enhanced when the second sequence was seen presented either to the hand or on a diagrammatic representation of a hand. A final experiment showed that the effects of Experiment 1 were replicated when the underside of the forearm was used for stimulus presentation, suggesting that the data are not idiosyncratic to the first method of presentation. The pattern of results suggests memory for a sequence of tactile stimuli involves the deployment of strategies utilising a combination of verbal rehearsal and visuo-spatial recoding rather than relying solely on the retention of sensory traces. This is taken to reflect limitations in both the capacity and duration of tactile sensory memory.     

Discrete and continuous measures of dimensional stimulus control

In two sets of experiments, we examined dimensional stimulus control of pigeons' responses to a visual flicker-rate continuum. In the first experiment, responses to a single key were reinforced periodically during stimuli from one half of the stimulus continuum, and responses during other stimuli were extinguished. In the second experiment, two response keys were simultaneously available, with reinforcement for each response alternative associated with different halves of the stimulus continuum. Conditions of the second experiment involved either free-operant or discrete-trial stimulus presentations. Results from these experiments show that positive dimensional contrast appeared in discrimination tasks with one or two response alternatives, but only with free-operant procedures. In addition, discrimination between stimulus classes established by differential reinforcement was assessed as accurately by continuous rate measures as by discrete response choice in the two-alternative situation. The general implication of these experiments is that response rate measures, when properly applied, may reveal sources of variation within stimulus classes, such as dimensional contrast, that are not evident with discrete measures.     

想象空间中物体搜索的阶段模型的证实

用因素实验证明,在故事阅读产生的想象场景中,位于其中的观察者对身体四周物体的搜索分为两个阶段：第一阶段是目标方位的判断,认知加工时间的模式是前＜后＜左＝右;第二阶段是注意指向目标方位,从而辨别目标物体,认知加工时间的模式是注意点＜注意点对面＜注意点左侧＝注意点右侧。这两个阶段没有交互作用。反应时依赖于被试的视点。     

Dissociations between categorization and similarity judgments as a result of learning feature distributions

A dissociation between categorization and similarity was found by Rips (1989). In one experiment, Rips found that a stimulus halfway between a pizza and a quarter was categorized as a pizza but was rated as more similar to a quarter. Smith and Sloman (1994) discussed these results in terms of the role of necessary and characteristic features. In two experiments, participants had to learn to categorize novel artificial shapes composed of a nonsalient necessary feature combined with a salient characteristic feature. Participants categorized stimuli on the basis of a necessary feature, whereas their similarity judgments relied on characteristic features. The role of deep (essential) features in dissociations is considered. Results are discussed in terms of the differences between requirements of categorization and similarity judgments.     

Interference in visual perception by verbal and spatial cognitive activity

In two experiments we tested the hypothesis that cognitive processing based on spatial imagery produces more deterioration of visual perception than cognitive processing based on verbal codes. So, we studied the effect on visual perception of two cognitive tasks, one of spatial imagery and the other a verbal task. In the first one, with 30 participants, we analyzed the mental load and ocular behaviors in both cognitive tasks. In the second experiment, with 29 participants, we studied the effect of both tasks on a visual search task, using a dual-task experimental paradigm. The verbal task presented higher mental load than the imagery task when both tasks were carried out with visual search task, and there was more deterioration in stimulus detection with the verbal task. We can conclude that: (1) cognitive tasks produce important deterioration in the capacities of visual search and identification of stimuli; (2) this deterioration has two components: (a) an inefficient search, associated with alterations of the gaze patterns while performing cognitive tasks, and (b) a general interference, nonspecific to spatial codes, in the process of identification of looked-at stimuli; (3) this cognitive interference is related to the mental load or effort required by the cognitive task.     

How does information from low and high spatial frequencies interact during scene categorization?

Current models of visual perception suggest that, during scene categorization, low spatial frequencies (LSF) are rapidly processed and activate plausible interpretations of visual input. This coarse analysis would be used to guide subsequent processing of high spatial frequencies (HSF). The present study aimed to further examine how information from LSF and HSF interact and influence each other during scene categorization. In a first experimental session, participants had to categorize LSF and HSF filtered scenes belonging to two different semantic categories (artificial vs. natural). In a second experimental session, we used hybrid scenes as stimuli made by combining LSF and HSF from two different scenes which were semantically similar or dissimilar. Half of the participants categorized LSF scenes in hybrids, and the other half categorized HSF scenes in hybrids. Stimuli were presented for 30 or 100?ms. Session 1 results showed better performance for LSF than HSF scene categorization. Session 2 scene categorization was faster when participants attended and categorized LSF than HSF scene in hybrids. The semantic interference of a semantically dissimilar HSF scene on LSF scene categorization was greater than the semantic interference of a semantically dissimilar LSF scene on HSF scene categorization, irrespective of exposure duration. These results suggest a LSF advantage for scene categorization, and highlight the prominent role of HSF information when there is uncertainty about the visual stimulus, in order to disentangle between alternative interpretations.