Vision function in children 10 years after grade 3 or 4 intraventricular haemorrhage with ventricular dilation: A masked prospective study.

AIM: We examined children 10 to 11 years after grade 3 or 4 intraventricular haemorrhage and ventricular dilation (IVHVD) and investigated whether the grade of IVHVD affected their visual outcome. We explored associations between visual outcomes with cognitive outcomes and extra support at school. METHOD: The visual examinations were part of a 10-year follow-up study for children in a randomized trial. Testers followed a protocol and were masked to whether the child had experienced grade 3 or grade 4 IVHVD and all other data. RESULTS: Thirty-two children were tested: 24 were male and mean (standard deviation) age was 10 years 5 months (1 year 2 months); range 8 years 9 months to 12 years 9 months. All had at least one visual impairment. The median (interquartile range) number of impairments per child was six (six to nine) for children who experienced a grade 4 IVHVD compared with three (two to four) for children who experienced a grade 3 IVHVD (p = 0.003). Each extra vision impairment per child was associated with increased educational support at school, after adjustment for developmental age equivalence (odds ratio = 1.7 [95% confidence interval 1.1-2.6], p = 0.015). INTERPRETATION: Children who experience grade 3 or 4 IVHVD have a high level of visual morbidity at age 10 to 11 years. These children may have unmet visual needs and their outcomes might improve if these needs could be addressed. WHAT THIS PAPER ADDS: Parent-reported questionnaire responses underestimated directly assessed visual morbidity. Grade 4 intraventricular haemorrhage and ventricular dilatation (IVHVD) was followed by more vision impairments than grade 3 IVHVD. Simple tests of visual perceptual skills correlated with the neuropsychology tests. Children with supranuclear eye movement disorders were more likely to be receiving extra help at school. Each additional visual impairment increased the likelihood of extra educational support.

Stimulus uncertainty predicts serial dependence in orientation judgements.

How is what you see influenced by what you saw? The visual system may use recent perception to inform responses to current stimuli. This can cause the perception of current stimuli to be attracted toward previous observations, an effect termed serial dependence. This misperception might well be useful in a noisy visual environment, where minor image distortions over time may not actually represent meaningful change. Previous work has suggested that Bayesian perceptual inference may underlie serial dependence. For this to be true, the relative uncertainty associated with both prior and current sensory input should be taken into account. In an experiment manipulating the level of noise present in orientation stimuli, we found an effect of current stimulus uncertainty on serial dependence. We found no good evidence for an effect of previous stimulus uncertainty. Our results provide only partial evidence for the Bayesian interpretation of serial dependence. Non-Bayesian models may provide a better account of the phenomenon.

Representation of facial identity includes expression variability.

In this study, we investigate the contribution of expression variability in the formation of face representations. We trained participants to learn new identities from face images either low or high in expressiveness, and compared their performance in a recognition test. After low expressiveness training, recognition of novel test images was modulated by image expressiveness: the more expressive the image, the slower the response. This differed from recognition after high expressiveness training, which showed little evidence of expression dependence. These findings are not readily explained by exemplar and prototype theories of face representation. However, we propose that our results can be explained by a combination of these theories, according to which average and exemplar representations co-exist - the latter of which preserve expressions and other within-person variability. We conclude that this study provides evidence that variability of expressions is, therefore, incorporated in the representation of an individual's face. Moreover, our results demonstrate that learning to recognise someone from their face entails learning how their face is changed by expressions.

Expressive Faces Confuse Identity.

We used highly variable, so-called 'ambient' images to test whether expressions affect the identity recognition of real-world facial images. Using movie segments of two actors unknown to our participants, we created image pairs - each image within a pair being captured from the same film segment. This ensured that, within pairs, variables such as lighting were constant whilst expressiveness differed. We created two packs of cards, one containing neutral face images, the other, their expressive counterparts. Participants sorted the card packs into piles, one for each perceived identity. As with previous studies, the perceived number of identities was higher than the veridical number of two. Interestingly, when looking within piles, we found a strong difference between the expressive and neutral sorting tasks. With expressive faces, identity piles were significantly more likely to contain cards of both identities. This finding demonstrates that, over and above other image variables, expressiveness variability can cause identity confusion; evidently, expression is not disregarded or factored out when we classify facial identity in real-world images. Our results provide clear support for a face processing architecture in which both invariant and changeable facial information may be drawn upon to drive our decisions of identity.

Expression Dependence in the Perception of Facial Identity.

We recognise familiar faces irrespective of their expression. This ability, crucial for social interactions, is a fundamental feature of face perception. We ask whether this constancy of facial identity may be compromised by changes in expression. This, in turn, addresses the issue of whether facial identity and expression are processed separately or interact. Using an identification task, participants learned the identities of two actors from naturalistic (so-called ambient) face images taken from movies. Training was either with neutral images or their expressive counterparts, perceived expressiveness having been determined experimentally. Expressive training responses were slower and more erroneous than neutral training responses. When tested with novel images of the actors that varied in expressiveness, neutrally trained participants gave slower and less accurate responses to images of high compared with low expressiveness. These findings clearly demonstrate that facial expressions impede the processing and learning of facial identity. Because this expression dependence is consistent with a late bifurcation model of face processing, in which changeable facial aspects and identity are coded in a common framework, it suggests that expressions are a part of facial identity representation.

Perceived duration of brief visual events is mediated by timing mechanisms at the global stages of visual processing.

There is a growing body of evidence pointing to the existence of modality-specific timing mechanisms for encoding sub-second durations. For example, the duration compression effect describes how prior adaptation to a dynamic visual stimulus results in participants underestimating the duration of a sub-second test stimulus when it is presented at the adapted location. There is substantial evidence for the existence of both cortical and pre-cortical visual timing mechanisms; however, little is known about where in the processing hierarchy the cortical mechanisms are likely to be located. We carried out a series of experiments to determine whether or not timing mechanisms are to be found at the global processing level. We had participants adapt to random dot patterns that varied in their motion coherence, thus allowing us to probe the visual system at the level of motion integration. Our first experiment revealed a positive linear relationship between the motion coherence level of the adaptor stimulus and duration compression magnitude. However, increasing the motion coherence level in a stimulus also results in an increase in global speed. To test whether duration compression effects were driven by global speed or global motion, we repeated the experiment, but kept global speed fixed while varying motion coherence levels. The duration compression persisted, but the linear relationship with motion coherence was absent, suggesting that the effect was driven by adapting global speed mechanisms. Our results support previous claims that visual timing mechanisms persist at the level of global processing.

Aftereffects support opponent coding of expression.

We used aftereffects to investigate the coding mechanisms underlying perception of facial expression. Recent evidence that some dimensions are common to the coding of both expression and identity suggests that the same type of coding system could be used for both attributes. Identity is adaptively opponent coded by pairs of neural populations tuned to opposite extremes of relevant dimensions. Therefore, the authors hypothesized that expression would also be opponent coded. An important line of support for opponent coding is that aftereffects increase with adaptor extremity (distance from an average test face) over the full natural range of possible faces. Previous studies have reported that expression aftereffects increase with adaptor extremity. Critically, however, they did not establish the extent of the natural range and so have not ruled out a decrease within that range that could indicate narrowband, multichannel coding. Here the authors show that expression aftereffects, like identity aftereffects, increase linearly over the full natural range of possible faces and remain high even for impossibly distorted adaptors. These results suggest that facial expression, like face identity, is opponent coded. (PsycINFO Database Record

Perceived Duration Increases with Contrast, but Only a Little.

Recent adaptation studies provide evidence for early visual areas playing a role in duration perception. One explanation for the pronounced duration compression commonly found with adaptation is that it reflects adaptation-driven stimulus-specific reduction in neural activity in early visual areas. If this level of stimulus-associated neural activity does drive duration, then we would expect a strong effect of contrast on perceived duration as electrophysiological studies shows neural activity in early visual areas to be strongly related to contrast. We employed a spatially isotropic noise stimulus where the luminance of each noise element was independently sinusoidally modulated at 4 Hz. Participants matched the perceived duration of a high (0.9) or low (0.1) contrast stimulus to a previously presented standard stimulus (600 ms, contrast = 0.3). To achieve perceptually equivalent durations, the low contrast stimulus had to be presented for longer than the high contrast stimulus. This occurred when we controlled for stimulus size and when we adjusted for individual differences in perceived temporal frequency. Further, we show that the effect cannot be explained by shifts in perceived onset and offset and is not explained by a simple contrast-driven response bias. The direction of our results is clearly consistent with the idea that level of neural activity drives duration. However, the magnitude of the effect (~10% duration difference over a 0.9-0.1 contrast reduction) is in marked contrast to the larger duration distortions that can be found with repetition suppression and the oddball effect; particularly when these may be associated with smaller differences in neural activity than that expected from our contrast difference. Taken together, these results indicate that level of stimulus-related neural activity in early visual areas is unlikely to provide a general mechanism for explaining differences in perceived duration.

Biological movement and the encoding of its motion and orientation.

Are you walking at me? Biological movement and the encoding of its motion and orientation. A person's motion conveys a wealth of information that ranges from the complex, such as intention or emotional state, to the simple, such as direction of locomotion. How we recognise and recover people's motion is addressed by models of biological motion processing. Single channel models propose that this occurs through the operation of form template neurons which respond to viewpoint dependent snapshots of posture. More controversially, a dual channel approach proposes a second stream containing motion template neurons sensitive to view dependent snapshots of biological movement's characteristic local velocity field. We used behavioural adaptation to look for the co-encoding of viewpoint and walker motion, a hallmark of motion template analysis. We show that opposite viewpoint aftereffects can simultaneously be induced for forwards and reversed walkers. This demonstrates that distinct populations of neurons encode forwards and reversed walking. To account for such aftereffects, these units must either be able to inhibit viewpoint-encoding neurons, or they must encode viewpoint directly. Whereas current single channel models would need extending to incorporate these characteristics, the idea that walker motion is encoded directly, such that viewpoint and motion are intrinsically interlinked, is a fundamental component of the dual channel model.

Adapting to time: Duration channels do not mediate human time perception.

Accurately encoding the duration and temporal order of events is essential for survival and important to everyday activities, from holding conversations to driving in fast-flowing traffic. Although there is a growing body of evidence that the timing of brief events (< 1 s) is encoded by modality-specific mechanisms, it is not clear how such mechanisms register event duration. One approach gaining traction is a channel-based model; this envisages narrowly-tuned, overlapping timing mechanisms that respond preferentially to different durations. The channel-based model predicts that adapting to a given event duration will result in overestimating and underestimating the duration of longer and shorter events, respectively. We tested the model by having observers judge the duration of a brief (600 ms) visual test stimulus following adaptation to longer (860 ms) and shorter (340 ms) stimulus durations. The channel-based model predicts perceived duration compression of the test stimulus in the former condition and perceived duration expansion in the latter condition. Duration compression occurred in both conditions, suggesting that the channel-based model does not adequately account for perceived duration of visual events.

Deciding on race: a diffusion model analysis of race-categorisation.

It has long been known that a person's race can affect their decisions about people of another race; an observation that clearly taps into some deep societal issues. However, in order to behave differently in response to someone else's race, you must first categorise that person as other-race. The current study investigates the process of race-categorisation. Two groups of participants, Asian and Caucasian, rapidly classified facial images that varied from strongly Asian, through racially intermediate, to strongly Caucasian. In agreement with previous findings, there was a difference in category boundary between the two groups. Asian participants more frequently judged intermediate images as Caucasian and vice versa. We fitted a decision model, the Ratcliff diffusion model, to our two choice reaction time data. This model provides an account of the processes thought to underlie binary choice decisions. Within its architecture it has two components that could reasonably lead to a difference in race category boundary, these being evidence accumulation rate and a priori bias. The latter is the expectation or prior belief that a participant brings to the task, whilst the former indexes sensitivity to race-dependent perceptual cues. Whilst we find no good evidence for a difference in a priori bias between our two groups, we do find evidence for a difference in evidence accumulation rate. Our Asian participants were more sensitive to Caucasian cues within the images than were our Caucasian participants (and vice versa). These results support the idea that differences in perceptual sensitivity to race-defining visual characteristics drive differences in race categorisation. We propose that our findings fit with a wider view in which perceptual adaptation plays a central role in the visual processing of own and other race.

Proximal-distal, not medial-lateral, movement across an edge increases discrimination of edge sharpness.

Edges are fundamental properties of our environment and the objects we interact with. There is a lack of research on the haptic perception of edges, especially the sharpness of an edge. Skinner et al. [2013 PLoS ONE, 8(9): e73283] found that haptic discriminability of sharpness was clearly superior when using a relatively unrestrained, free exploration strategy compared with a static single touch strategy. In the free exploration condition two distinct movement patterns were frequently used by participants: a proximal-distal movement of the fingerpad across the test edge and a medial-lateral movement of the fingerpad along the test edge. Here, using the same stimuli and two-alternative forced-choice method of constant stimuli as Skinner et al. (2013), we demonstrate that a proximal-distal movement results in substantially lower sharpness discrimination thresholds than a medial-lateral movement. The underlying neurophysiology and implications for the design of haptic displays are considered.

Direction-contingent duration compression is primarily retinotopic.

Previous research has shown that prior adaptation to a spatially circumscribed, oscillating grating results in the duration of a subsequent stimulus briefly presented within the adapted region being underestimated. There is an on-going debate about where in the motion processing pathway the adaptation underlying this distortion of sub-second duration perception occurs. One position is that the LGN and, perhaps, early cortical processing areas are likely sites for the adaptation; an alternative suggestion is that visual area MT+ contains the neural mechanisms for sub-second timing; and a third position proposes that the effect is driven by adaptation at multiple levels of the motion processing pathway. A related issue is in what frame of reference - retinotopic or spatiotopic - does adaptation induced duration distortion occur. We addressed these questions by having participants adapt to a unidirectional random dot kinematogram (RDK), and then measuring perceived duration of a 600 ms test RDK positioned in either the same retinotopic or the same spatiotopic location as the adaptor. We found that, when it did occur, duration distortion of the test stimulus was direction contingent; that is it occurred when the adaptor and test stimuli drifted in the same direction, but not when they drifted in opposite directions. Furthermore the duration compression was evident primarily under retinotopic viewing conditions, with little evidence of duration distortion under spatiotopic viewing conditions. Our results support previous research implicating cortical mechanisms in the duration encoding of sub-second visual events, and reveal that these mechanisms encode duration within a retinotopic frame of reference.

On the edge: haptic discrimination of edge sharpness.

The increasing ubiquity of haptic displays (e.g., smart phones and tablets) necessitates a better understanding of the perceptual capabilities of the human haptic system. Haptic displays will soon be capable of locally deforming to create simple 3D shapes. This study investigated the sensitivity of our haptic system to a fundamental component of shapes: edges. A novel set of eight high quality shape stimuli with test edges that varied in sharpness were fabricated in a 3D printer. In a two alternative, forced choice task, blindfolded participants were presented with two of these shapes side by side (one the reference, the other selected randomly from the remaining set of seven) and after actively exploring the test edge of each shape with the tip of their index finger, reported which shape had the sharper edge. We used a model selection approach to fit optimal psychometric functions to performance data, and from these obtained just noticeable differences and Weber fractions. In Experiment 1, participants performed the task with four different references. With sharpness defined as the angle at which one surface meets the horizontal plane, the four JNDs closely followed Weber's Law, giving a Weber fraction of 0.11. Comparisons to previously reported Weber fractions from other haptic manipulations (e.g. amplitude of vibration) suggests we are sufficiently sensitive to changes in edge sharpness for this to be of potential utility in the design of future haptic displays. In Experiment 2, two groups of participants performed the task with a single reference but different exploration strategies; one was limited to a single touch, the other unconstrained and free to explore as they wished. As predicted, the JND in the free exploration condition was lower than that in the single touch condition, indicating exploration strategy affects sensitivity to edge sharpness.

Processing of fear and anger facial expressions: the role of spatial frequency.

Spatial frequency (SF) components encode a portion of the affective value expressed in face images. The aim of this study was to estimate the relative weight of specific frequency spectrum bandwidth on the discrimination of anger and fear facial expressions. The general paradigm was a classification of the expression of faces morphed at varying proportions between anger and fear images in which SF adaptation and SF subtraction are expected to shift classification of facial emotion. A series of three experiments was conducted. In Experiment 1 subjects classified morphed face images that were unfiltered or filtered to remove either low (<8 cycles/face), middle (12-28 cycles/face), or high (>32 cycles/face) SF components. In Experiment 2 subjects were adapted to unfiltered or filtered prototypical (non-morphed) fear face images and subsequently classified morphed face images. In Experiment 3 subjects were adapted to unfiltered or filtered prototypical fear face images with the phase component randomized before classifying morphed face images. Removing mid frequency components from the target images shifted classification toward fear. The same shift was observed under adaptation condition to unfiltered and low- and middle-range filtered fear images. However, when the phase spectrum of the same adaptation stimuli was randomized, no adaptation effect was observed. These results suggest that medium SF components support the perception of fear more than anger at both low and high level of processing. They also suggest that the effect at high-level processing stage is related more to high-level featural and/or configural information than to the low-level frequency spectrum.

Nine-year-old children use norm-based coding to visually represent facial expression.

Children are less skilled than adults at making judgments about facial expression. This could be because they have not yet developed adult-like mechanisms for visually representing faces. Adults are thought to represent faces in a multidimensional face-space, and have been shown to code the expression of a face relative to the norm or average face in face-space. Norm-based coding is economical and adaptive, and may be what makes adults more sensitive to facial expression than children. This study investigated the coding system that children use to represent facial expression. An adaptation aftereffect paradigm was used to test 24 adults and 18 children (9 years 2 months to 9 years 11 months old). Participants adapted to weak and strong antiexpressions. They then judged the expression of an average expression. Adaptation created aftereffects that made the test face look like the expression opposite that of the adaptor. Consistent with the predictions of norm-based but not exemplar-based coding, aftereffects were larger for strong than weak adaptors for both age groups. Results indicate that, like adults, children's coding of facial expressions is norm-based.

The expressions of strangers: our identity-independent representation of facial expression.

Evidence suggests that underlying the human system processing facial expressions are two types of representation of expression: one dependent on identity and the other independent of identity. We recently presented findings indicating that identity-dependent representations are encoded using a prototype-referenced scheme, in a manner notably similar to that proposed for facial identity. Could it be that identity-independent representations are encoded this way too? We investigated this by adapting participant to anti-expressions and asking them to categorize the expression aftereffect in a prototype probe that was either the same (congruent) or different (incongruent) identity to that of the adapter. To distinguish between encoding schemes, we measured how aftereffect magnitude changed in response to variations in the strength of adapters. The increase in aftereffect magnitude with adapter strength characteristic of prototype-referenced encoding was observed in both congruent and, crucially, incongruent conditions. We conclude that identity-independent representations of expression are indeed encoded using a prototype-referenced scheme. The striking similarity between the encoding of facial identity and both representations of expression raises the possibility that prototype-referenced encoding might be a common scheme for encoding the many types of information in faces needed to enable our complex social interactions.

The many directions of time.

Event duration perception is fundamental to cognitive functioning. Recent research has shown that localized sensory adaptation compresses perceived duration of brief visual events in the adapted location; however, there is disagreement on whether the source of these temporal distortions is cortical or pre-cortical. The current study reveals that spatially localized duration compression can also be direction contingent, in that duration compression is induced when adapting and test stimuli move in the same direction but not when they move in opposite directions. Because of its direction-contingent nature, the induced duration compression reported here is likely to be cortical in origin. A second experiment shows that the adaptation processes driving duration compression can occur at or beyond human cortical area MT+, a specialized motion center located upstream from primary visual cortex. The direction-specificity of these temporal mechanisms, in conjunction with earlier reports of pre-cortical temporal mechanisms driving duration perception, suggests that our encoding of subsecond event duration is driven by activity at multiple levels of processing.

Testing a simplified method for measuring velocity integration in saccades using a manipulation of target contrast.

A growing number of studies in vision research employ analyses of how perturbations in visual stimuli influence behavior on single trials. Recently, we have developed a method along such lines to assess the time course over which object velocity information is extracted on a trial-by-trial basis in order to produce an accurate intercepting saccade to a moving target. Here, we present a simplified version of this methodology, and use it to investigate how changes in stimulus contrast affect the temporal velocity integration window used when generating saccades to moving targets. Observers generated saccades to one of two moving targets which were presented at high (80%) or low (7.5%) contrast. In 50% of trials, target velocity stepped up or down after a variable interval after the saccadic go signal. The extent to which the saccade endpoint can be accounted for as a weighted combination of the pre- or post-step velocities allows for identification of the temporal velocity integration window. Our results show that the temporal integration window takes longer to peak in the low when compared to high contrast condition. By enabling the assessment of how information such as changes in velocity can be used in the programming of a saccadic eye movement on single trials, this study describes and tests a novel methodology with which to look at the internal processing mechanisms that transform sensory visual inputs into oculomotor outputs.

Effects of 7.5% CO(2) inhalation on allocation of spatial attention to facial cues of emotional expression.

Increased vigilance to threat-related stimuli is thought to be a core cognitive feature of anxiety. We sought to investigate the cognitive impact of experimentally induced anxiety, by means of a 7.5% CO(2) challenge, which acts as an unconditioned anxiogenic stimulus, on attentional bias for positive and negative facial cues of emotional expression in the dot-probe task. In two experiments we found robust physiological and subjective effects of the CO(2) inhalation consistent with the claim that the procedure reliably induces anxiety. Data from the dot-probe task demonstrated an attentional bias to emotional facial expressions compared with neutral faces regardless of valence (happy, angry, and fearful). These attentional effects, however, were entirely inconsistent in terms of their relationship with induced anxiety. We conclude that the previously reported poor reliability of this task is the most parsimonious explanation for our conflicting findings and that future research should develop a more reliable paradigm for measuring attentional bias in this field.