Stimulus Configuration Research Articles

The influence of spatial pattern on visual short-term memory for contrast

Several psychophysical studies of visual short-term memory (VSTM) have shown high-fidelity storage capacity for many properties of visual stimuli. On judgments of the spatial frequency of gratings, for example, discrimination performance does not decrease significantly, even for memory intervals of up to 30 s. For other properties, such as stimulus orientation and contrast, however, such “perfect storage” behavior is not found, although the reasons for this difference remain unresolved. Here, we report two experiments in which we investigated the nature of the representation of stimulus contrast in VSTM using spatially complex, two-dimensional random-noise stimuli. We addressed whether information about contrast per se is retained during the memory interval by using a test stimulus with the same spatial structure but either the same or the opposite local contrast polarity, with respect to the comparison (i.e., remembered) stimulus. We found that discrimination thresholds got steadily worse with increasing duration of the memory interval. Furthermore, performance was better when the test and comparison stimuli had the same local contrast polarity than when they were contrast-reversed. Finally, when a noise mask was introduced during the memory interval, its disruptive effect was maximal when the spatial configuration of its constituent elements was uncorrelated with those of the comparison and test stimuli. These results suggest that VSTM for contrast is closely tied to the spatial configuration of stimuli and is not transformed into a more abstract representation.

Revisiting the Lissajous figure as a tool to study bistable perception

During bistable vision perception spontaneously "switches" between two mutually exclusive percepts despite constant sensory input. The endogenous nature of these perceptual transitions has motivated extensive research aimed at the underlying mechanisms, since spontaneous perceptual transitions of bistable stimuli should in principle allow for a dissociation of processes related to sensory stimulation from those related to conscious perception. However, transitions from one conscious percept to another are often not instantaneous, and participants usually report a considerable amount of mixed or unclear percepts. This feature of bistable vision makes it difficult to isolate transition-related visual processes. Here, we revisited an ambiguous depth-from-motion stimulus which was first introduced to experimental psychology more than 80 years ago. This rotating Lissajous figure might prove useful in complementing other bistable stimuli, since its perceptual transitions only occur at critical stimulus configurations and are virtually instantaneous, thus facilitating the construction of a perceptually equivalent replay condition. We found that three parameters of the Lissajous figure - complexity, line width, and rotational speed - differentially modulated its perceptual dominance durations and transition probabilities, thus providing experimenters with a versatile tool to study the perceptual dynamics of bistable vision.

An Active Thin-Film Cochlear Electrode Array With Monolithic Backing and Curl

This paper reports the development of a robust, 32-site, four-channel, flexible cochlear implant as a prototype for a 128-site, eight-channel human prosthesis. The electrode array is comprised of metal layers embedded in Parylene C and includes parylene rings and self-curling parylene layers that can achieve a minimum radius of curvature . Finite element analysis simulations predict that the substrate stiffness of the arrays can be tailored from 0.2 to 1.4 kN·μm2 with parylene rings to increase the rigidity seven-fold over that of a flat parylene array. Guinea pig arrays have achieved insertion depths of up to 6.5 mm in the cochlea with no visible damage to the scala media. The application specific integrated circuit (ASIC) for the cochlear implant was realized in 0.5 μm technology to support a wide range of multisite multipolar stimulus configurations. The ASIC fits within the space of the otic bulla with a size of 2.2 mm by 2.5 mm and operates from a ±2.5 V supply at clock speeds up to 500 kHz. The maximum power consumption is 2.5 mW when outputting monopolar 500 μA biphasic pulses.

A Causal Perspective on the Analysis of Signal and Noise Correlations and Their Role in Population Coding

The role of correlations between neuronal responses is crucial to understanding the neural code. A framework used to study this role comprises a breakdown of the mutual information between stimuli and responses into terms that aim to account for different coding modalities and the distinction between different notions of independence. Here we complete the list of types of independence and distinguish activity independence (related to total correlations), conditional independence (related to noise correlations), signal independence (related to signal correlations), coding independence (related to information transmission), and information independence (related to redundancy). For each type, we identify the probabilistic criterion that defines it, indicate the information-theoretic measure used as statistic to test for it, and provide a graphical criterion to recognize the causal configurations of stimuli and responses that lead to its existence. Using this causal analysis, we first provide sufficiency conditions relating these types. Second, we differentiate the use of the measures as statistics to test for the existence of independence from their use for quantification. We indicate that signal and noise correlation cannot be quantified separately. Third, we explicitly define alternative system configurations used to construct the measures, in which noise correlations or noise and signal correlations are eliminated. Accordingly, we examine which measures are meaningful only as a comparison across configurations and which ones provide a characterization of the actually observed responses without resorting to other configurations. Fourth, we compare the commonly used nonparametric approach to eliminate noise correlations with a functional (model-based) approach, showing that the former approach does not remove those effects of noise correlations captured by the tuning properties of the individual neurons, and implies nonlocal causal structure manipulations. These results improve the interpretation of the measures on the framework and help in understanding how to apply it to analyze the role of correlations.

Need for Space: The Key Distance Effect Depends on Spatial Stimulus Configurations

In numerous psychological experiments, participants classify stimuli by pressing response keys. According to Lakens, Schneider, Jostmann, and Schubert (2011), classification performance is affected by physical distance between response keys – indicating a cognitive tendency to represent categories in spatial code. However, previous evidence for a key distance effect (KDE) from a color-naming Stroop task is inconclusive as to whether: (a) key separation automatically leads to an internal spatial representation of non-spatial stimulus characteristics in participants, or if the KDE rather depends on physical spatial characteristics of the stimulus configuration; (b) the KDE attenuates the Stroop interference effect. We therefore first adopted the original Stroop task in Experiment 1, confirming that wider key distance facilitated responses, but did not modulate the Stroop effect as was previously found. In Experiments 2 and 3 we controlled potential mediator variables in the original design. When we did not display instructions about stimulus-response mappings, thereby removing the unintended spatial context from the Stroop stimuli, no KDE emerged. Presenting the instructions at a central position in Experiment 4 confirmed that key separation alone is not sufficient for a KDE, but correspondence between spatial configurations of stimuli and responses is also necessary. Evidence indicates that the KDE on Stroop performance is due to known mechanisms of stimulus-response compatibility and response discriminability. The KDE does, however, not demonstrate a general disposition to represent any stimulus in spatial code.

Attentional tradeoffs in the pigeon

We deployed the Multiple Necessary Cues (MNC) discrimination task to see if pigeons can simultaneously attend to four different dimensions of complex visual stimuli. Specifically, we trained nine pigeons (Columba livia) on a go/no go discrimination to peck only 1 of 16 compound stimuli created from all possible combinations of two stimulus values from four separable visual dimensions: shape (circle/square), size (large/small), line orientation (horizontal/vertical), and brightness (dark/light). Some of the pigeons had CLHD (circle, large, horizontal, dark) as the positive stimulus (S+), whereas others had SSVL (square, small, vertical, light) as the S+. We recorded touchscreen pecking during the first 15 s that each stimulus was presented on each training trial. Discrimination training continued until pigeons' rates of responding to all 15 negative stimuli (S-s) fell to less than 15% of their response rates to the S+. All pigeons acquired the MNC discrimination, suggesting that they attended to all four dimensions of the multidimensional stimuli. Learning rate was similar for all four dimensions, indicating equivalent salience of the discriminative stimuli. The more dimensions along which the S-s differed from the S+, the faster was discrimination learning, suggesting an added benefit from increasing perceptual disparities of the S-s from the S+. Finally, evidence of attentional tradeoffs among the four dimensions was seen during discrimination learning, raising interesting questions concerning the possible control of behavior by elemental and configural stimuli.

The enigma of Bálint's syndrome: neural substrates and cognitive deficits

The enigma of Bálint's syndrome: neural substrates and cognitive deficits

Contrast–contrast asynchronies

We introduce the "contrast-contrast asynchrony," a dynamic stimulus configuration that combines elements of the Shapiro contrast asynchrony with elements of the Chubb contrast-contrast illusion. In the contrast-contrast asynchrony, static textured fields surround two textured fields; one surround has high-contrast texture, and the other has low-contrast texture. The contrasts of the center fields modulate in phase with each other at 1 Hz, and as a consequence, the difference between the contrast of the centers and the contrast of the respective surround modulates in antiphase. Most observers report an antiphase appearance for high-contrast, fine-grained centers. These observers therefore respond to the difference between the center contrast and surround contrast. We also document three observers who do not see the asynchrony for high-contrast modulations of the center, suggesting possibly interesting individual differences.

Orienting attention in visual working memory requires central capacity: Decreased retro-cue effects under dual-task conditions

The retro-cue effect (RCE) describes superior working memory performance for validly cued stimulus locations long after encoding has ended. Importantly, this happens with delays beyond the range of iconic memory. In general, the RCE is a stable phenomenon that emerges under varied stimulus configurations and timing parameters. We investigated its susceptibility to dual-task interference to determine the attentional requirements at the time point of cue onset and encoding. In Experiment 1, we compared single- with dual-task conditions. In Experiment 2, we borrowed from the psychological refractory period paradigm and compared conditions with high and low (dual-) task overlap. The secondary task was always binary tone discrimination requiring a manual response. Across both experiments, an RCE was found, but it was diminished in magnitude in the critical dual-task conditions. A previous study did not find evidence that sustained attention is required in the interval between cue offset and test. Our results apparently contradict these findings and point to a critical time period around cue onset and briefly thereafter during which attention is required.

The Influence of Feature Conjunction on Object Inversion and Conversion Effects

The face inversion effect is considered by some as a marker ofholistic or configural processing. In an effort to understand the relations between object orientation and the use of configuration for recognition, we explored the extent to which the combination of information across discrete, spatially separated object features contributed to the impact of transforming the orientation of faces and other objects. Subjects performed a matching task on four different sets of faces and novel objects. For two of the sets (diagnostic), the match could be made based on information contained in a single feature. For the remaining two sets (conjunction and disjunction), the information useful for successful matching was divided between two spatially separated features (at the top and at the bottom of the object). For OR disjunctions the top and bottom features provided redundant information such that subjects could rely on either the top or the bottom feature, whereas for AND conjunctions the top and bottom features provided unique information such that subjects needed to use both the top and the bottom features. Experiment 1 assessed the cost of inversion on these stimulus sets with the typical inversion task, where both study and test stimuli were presented in the same orientation. Consistent with previous work, significant inversion effects were found for all of the face sets, but none of the novel object sets. Experiment 2 assessed the cost of 'conversion'--that is, the effect of transforming the orientation of the stimulus between study and test. Consistent with previous work, significant conversion effects were found for all face sets; however, a significant conversion effect was also found for the AND novel set. That only the AND novel set was significant suggests that conversion effects are reliant on combination of information across features, which is compromised when the stimulus configuration is altered between study and test. The results suggest that configural processes, like those purportedly used for face recognition, may be domain-general processes that can also be recruited strategically with other types of objects.

Influence of visual angle on pattern reversal visual evoked potentials.

Purpose:The aim of this study was to find whether the visual evoked potential (VEP) latencies and amplitude are altered with different visual angles in healthy adult volunteers or not and to determine the visual angle which is the optimum and most appropriate among a wide range of check sizes for the reliable interpretation of pattern reversal VEPs (PRVEPs).Materials and Methods:The present study was conducted on 40 healthy volunteers. The subjects were divided into two groups. One group consisted of 20 individuals (nine males and 11 females) in the age range of 25-57 years and they were exposed to checks subtending a visual angle of 90, 120, and 180 minutes of arc. Another group comprised of 20 individuals (10 males and 10 females) in the age range of 36-60 years and they were subjected to checks subtending a visual angle of 15, 30, and 120 minutes of arc. The stimulus configuration comprised of the transient pattern reversal method in which a black and white checker board is generated (full field) on a VEP Monitor by an Evoked Potential Recorder (RMS EMG. EPMARK II). The statistical analysis was done by One Way Analysis of Variance (ANOVA) using EPI INFO 6.Results:In Group I, the maximum (max.) P100 latency of 98.8 ± 4.7 and the max. P100 amplitude of 10.05 ± 3.1 μV was obtained with checks of 90 minutes. In Group II, the max. P100 latency of 105.19 ± 4.75 msec as well as the max. P100 amplitude of 8.23 ± 3.30 μV was obtained with 15 minutes. The min. P100 latency in both the groups was obtained with checks of 120 minutes while the min. P100 amplitude was obtained with 180 minutes. A statistically significant difference was derived between means of P100 latency for 15 and 30 minutes with reference to its value for 120 minutes and between the mean value of P100 amplitude for 120 minutes and that of 90 and 180 minutes.Conclusion:Altering the size of stimulus (visual angle) has an effect on the PRVEP parameters. Our study found that the 120 is the appropriate (and optimal) check size that can be used for accurate interpretation of PRVEPs. This will help in better assessment of the optic nerve function and integrity of anterior visual pathways.

Prism adaptation does not alter configural processing of faces

Patients with hemispatial neglect (‘neglect’) following a brain lesion show difficulty responding or orienting to objects and events on the left side of space. Substantial evidence supports the use of a sensorimotor training technique called prism adaptation as a treatment for neglect. Reaching for visual targets viewed through prismatic lenses that induce a rightward shift in the visual image results in a leftward recalibration of reaching movements that is accompanied by a reduction of symptoms in patients with neglect. The understanding of prism adaptation has also been advanced through studies of healthy participants, in whom adaptation to leftward prismatic shifts results in temporary neglect-like performance. Interestingly, prism adaptation can also alter aspects of non-lateralised spatial attention. We previously demonstrated that prism adaptation alters the extent to which neglect patients and healthy participants process local features versus global configurations of visual stimuli. Since deficits in non-lateralised spatial attention are thought to contribute to the severity of neglect symptoms, it is possible that the effect of prism adaptation on these deficits contributes to its efficacy. This study examines the pervasiveness of the effects of prism adaptation on perception by examining the effect of prism adaptation on configural face processing using a composite face task. The composite face task is a persuasive demonstration of the automatic global-level processing of faces: the top and bottom halves of two familiar faces form a seemingly new, unknown face when viewed together. Participants identified the top or bottom halves of composite faces before and after prism adaptation. Sensorimotor adaptation was confirmed by significant pointing aftereffect, however there was no significant change in the extent to which the irrelevant face half interfered with processing. The results support the proposal that the therapeutic effects of prism adaptation are limited to dorsal stream processing.

Illusory position shift induced by motion within a moving envelope during smooth-pursuit eye movements

The static envelope of a Gabor patch with a moving carrier appears to shift in the direction of the carrier motion; this phenomenon is known as the motion-induced position shift (De Valois & De Valois, 1991; Ramachandran & Anstis, 1990). This conventional stimulus configuration contains at least three covarying factors: the retinal carrier velocity, the environmental carrier velocity, and the carrier velocity relative to the envelope velocity, which happens to be zero. We manipulated these velocities independently to identify which is critical, and we measured the perceived position of the moving Gabor patch relative to a reference stimulus moving in the same direction at the same speed. In the first experiment, the position of the moving envelope observed with fixation appeared to shift in the direction of the carrier velocity relative to the envelope velocity. Furthermore, the illusion was more pronounced when the carrier moved in a direction opposite to that of the envelope. In the second and third experiments, we measured the illusion during smooth-pursuit eye movement in which the envelope was either static or moving, thereby dissociating retinal and environmental velocities. Under all conditions, the illusion occurred according to the envelope-relative velocity of the carrier. Additionally, the illusion was more pronounced when the carrier and envelope moved in opposite directions. We conclude that the carrier's envelope-relative velocity is the primary determinant of the motion-induced position shift.

Saccades Toward the Target Are Planned as Sequences Rather Than as Single Steps

To find a target during visual search, observers often need to make multiple eye movements, which results in a scan path. It is an open question whether the saccade destinations in scan paths are planned ahead. In the two experiments reported here, we investigated this question by focusing on the observer’s ability to deviate from potentially planned paths. In the first experiment, the stimulus configuration could change during the initial saccade. We found that the observer’s ability to deviate from potentially planned paths crucially depended on whether altered configurations could be processed with sufficient rapidity. In a follow-up experiment, we asked whether planned paths can include more than two saccade destinations. Investigating the influence of potentially planned paths on a secondary task demonstrated that planned paths can include at least three saccade destinations. Together, these experiments provide the first evidence of scan-path planning in visual search.

Technical clarification to Silbert and Thomas (2013): “Decisional separability, model identification, and statistical inference in the general recognition theory framework”

We offer a minor technical correction to the published proof of part (ii) of the main theorem in Silbert and Thomas (Psychonomic Bulletin & Review, 20, 1-20, 2013) that somewhat limits the scope of the equivalence observed in that work. Specifically, in order for a mean shift integrality with decisional separability to be mimicked by a perceptually separable but nondecisionally separable configuration, one needs to assume stimulus invariance. This holds when all of the covariance matrices in the stimulus configuration are equal to each other. We note that part (i) of the theorem is unaffected by this modification; an empirical finding of perceptual separability and the failure of decisional separability can be mimicked by a perceptually nonseparable, decisionally separable configuration without restricting the covariance matrices to be equal. We also note that stimulus invariance is often assumed in simple designs (e.g., Macmillan & Ornstein in Journal of the Acoustical Society of America, 97, 1261-1285, 1998), due to the implausibility of different perceptual correlations being present within stimuli perched very closely in perceptual space.

Prism adaptation does not alter configural processing of faces.

Patients with hemispatial neglect ('neglect') following a brain lesion show difficulty responding or orienting to objects and events on the left side of space. Substantial evidence supports the use of a sensorimotor training technique called prism adaptation as a treatment for neglect. Reaching for visual targets viewed through prismatic lenses that induce a rightward shift in the visual image results in a leftward recalibration of reaching movements that is accompanied by a reduction of symptoms in patients with neglect. The understanding of prism adaptation has also been advanced through studies of healthy participants, in whom adaptation to leftward prismatic shifts results in temporary neglect-like performance. Interestingly, prism adaptation can also alter aspects of non-lateralised spatial attention. We previously demonstrated that prism adaptation alters the extent to which neglect patients and healthy participants process local features versus global configurations of visual stimuli. Since deficits in non-lateralised spatial attention are thought to contribute to the severity of neglect symptoms, it is possible that the effect of prism adaptation on these deficits contributes to its efficacy. This study examines the pervasiveness of the effects of prism adaptation on perception by examining the effect of prism adaptation on configural face processing using a composite face task. The composite face task is a persuasive demonstration of the automatic global-level processing of faces: the top and bottom halves of two familiar faces form a seemingly new, unknown face when viewed together. Participants identified the top or bottom halves of composite faces before and after prism adaptation. Sensorimotor adaptation was confirmed by significant pointing aftereffect, however there was no significant change in the extent to which the irrelevant face half interfered with processing. The results support the proposal that the therapeutic effects of prism adaptation are limited to dorsal stream processing.

The separation of monocular and binocular contrast

The contrast asynchrony is a stimulus configuration that illustrates the visual system's separable responses to luminance and luminance contrast information (Shapiro, 2008; Shapiro et al., 2004). When two disks, whose luminances modulate in phase with each other, are each surrounded by a disk, one light and one dark, observers can see both the in-phase brightness signals and the antiphase contrast signals and can separate the two. Here we present the results of experiments in which observers viewed a similar stimulus dichoptically. We report that no asynchrony is perceived when one eye is presented with modulating disks and the other eye is presented with the black and white surround rings, nor is an asynchrony perceived in gradient versions of the contrast asynchrony. We also explore the "window shade illusion" (Shapiro, Charles, & Shear-Heyman, 2005) dichoptically and find that when a modulating disk is presented to one eye and a horizontally split black/white annulus is presented to the other, observers perceive a "shading" motion up and down the disk. This shading can be seen in either direction in the binocular condition, but it is almost always seen as moving towards low contrast in the monocular condition. These findings indicate the presence of separable retinal and cortical networks for contrast processing at different temporal and spatial scales.

Influence of auditory and audiovisual stimuli on the right–left prevalence effect

When auditory stimuli are used in two-dimensional spatial compatibility tasks, where the stimulus and response configurations vary along the horizontal and vertical dimensions simultaneously, a right-left prevalence effect occurs in which horizontal compatibility dominates over vertical compatibility. The right-left prevalence effects obtained with auditory stimuli are typically larger than that obtained with visual stimuli even though less attention should be demanded from the horizontal dimension in auditory processing. In the present study, we examined whether auditory or visual dominance occurs when the two-dimensional stimuli are audiovisual, as well as whether there will be cross-modal facilitation of response selection for the horizontal and vertical dimensions. We also examined whether there is an additional benefit of adding a pitch dimension to the auditory stimulus to facilitate vertical coding through use of the spatial-musical association of response codes (SMARC) effect, where pitch is coded in terms of height in space. In Experiment 1, we found a larger right-left prevalence effect for unimodal auditory than visual stimuli. Neutral, non-pitch coded, audiovisual stimuli did not result in cross-modal facilitation, but did show evidence of visual dominance. The right-left prevalence effect was eliminated in the presence of SMARC audiovisual stimuli, but the effect influenced horizontal rather than vertical coding. Experiment 2 showed that the influence of the pitch dimension was not in terms of influencing response selection on a trial-to-trial basis, but in terms of altering the salience of the task environment. Taken together, these findings indicate that in the absence of salient vertical cues, auditory and audiovisual stimuli tend to be coded along the horizontal dimension and vision tends to dominate audition in this two-dimensional spatial stimulus-response task.

Mastoid and vertex low-frequency vibration-induced oVEMP in relation to medially directed acceleration of the labyrinth

ObjectiveTo explore the stimulus site and stimulus configuration dependency for bone-conducted low-frequency vibration-induced ocular vestibular evoked myogenic potentials (oVEMPs). MethodsoVEMPs were tested in response to 125Hz single cycle bone-conducted vibration in healthy subjects (n=12) and in patients with severe unilateral vestibular lesions (n=10). The stimulus sites were the mastoids and vertex. Both directions of initial stimulus motion were used. ResultsAt mastoid stimulation, the oVEMP to initial laterally directed acceleration of the labyrinth was delayed approximately the length of time of a stimulus half-cycle, as compared with the response to initial medially directed acceleration. At vertex stimulation, the oVEMP to positive initial acceleration was similar to the oVEMP to mastoid stimulation causing lateral initial acceleration. Likewise, the oVEMP to vertex negative initial acceleration was similar to mastoid stimulation causing initial medial acceleration. Further, patients with unilateral vestibular loss had, compared to healthy subjects, similar oVEMP from the healthy labyrinth. ConclusionsA fundamental dependency on medially directed accelerations of the labyrinth, based on the latency differences revealed, may theoretically account for oVEMP in response to low-frequency stimulation. SignificanceLow-frequency bone vibration stimulation at vertex might serve for simultaneous oVEMP testing of both ears.

Does conflict frequency depending on stimulus configuration modulate compatibility effect?

Does conflict frequency depending on stimulus configuration modulate compatibility effect?