The Impact on Emotion Classification Performance and Gaze Behavior of Foveal versus Extrafoveal Processing of Facial Features

At normal interpersonal distances all features of a face cannot fall within one’s fovea simultaneously. Given that certain facial features are differentially informative of different emotions, does the ability to identify facially expressed emotions vary according to the feature fixated and do saccades preferentially seek diagnostic features? Previous findings are equivocal. We presented faces for a brief time, insufficient for a saccade, at a spatial position that guaranteed that a given feature – an eye, cheek, the central brow, or mouth – fell at the fovea. Across two experiments, observers were more accurate and faster at discriminating angry expressions when the high spatial-frequency information of the brow was projected to their fovea than when one or other cheek or eye was. Performance in classifying fear and happiness (Experiment 1) was not influenced by whether the most informative features (eyes and mouth, respectively) were projected foveally or extrafoveally. Observers more accurately distinguished between fearful and surprised expressions (Experiment 2) when the mouth was projected to the fovea. Reflexive first saccades tended towards the left and center of the face rather than preferentially targeting emotion-distinguishing features. These results reflect the integration of task-relevant information across the face constrained by the differences between foveal and extrafoveal processing (Peterson & Eckstein, 2012)

Beyond scattering and absorption: Perceptual un-mixing of translucent liquids

Is perception of translucence based on estimations of scattering and absorption of light or on statistical pseudocues associated with familiar materials? We compared perceptual performance with real and computer-generated stimuli. Real stimuli were glasses of milky tea. Milk predominantly scatters light and tea absorbs it, but since the tea absorbs less as the milk concentration increases, the effects of milkiness and strength on scattering and absorption are not independent. Conversely, computer-generated stimuli were glasses of “milky tea” in which absorption and scattering were independently manipulated. Observers judged tea concentrations regardless of milk concentrations, or vice versa. Maximum-likelihood conjoint measurement was used to estimate the contributions of each physical component—concentrations of milk and tea, or amounts of scattering and absorption—to perceived milkiness or tea strength. Separability of the two physical dimensions was better for real than for computer-generated teas, suggesting that interactions between scattering and absorption were correctly accounted for in perceptual unmixing, but unmixing was always imperfect. Since the real and rendered stimuli represent different physical processes and therefore differ in their image statistics, perceptual judgments with these stimuli allowed us to identify particular pseudocues (presumably learned with real stimuli) that explain judgments with both stimulus sets

A medieval multiverse?: Mathematical modelling of the thirteenth century universe of Robert Grosseteste

In his treatise on light, written about 1225, Robert Grosseteste describes a cosmological model in which the universe is created in a big-bang-like explosion and subsequent condensation. He postulates that the fundamental coupling of light and matter gives rises to the material body of the entire cosmos. Expansion is arrested when matter reaches a minimum density and subsequent emission of light from the outer region leads to compression and rarefaction of the inner bodily mass so as to create nine celestial spheres, with an imperfect residual core. In this paper, we reformulate the Latin description in terms of a modern mathematical model, teasing out consequences implicit in the text, but which the author would not have had the tools to explore. The equations which describe the coupling of light and matter are solved numerically, subjected to initial conditions and critical criteria consistent with the text. Formation of a universe with a non-infinite number of perfected spheres is extremely sensitive to the initial conditions, the intensity of the light and the transparency of these spheres. In this ‘medieval multiverse’, only a small range of opacity and initial density profiles leads to a stable universe with nine perfected spheres. As in current cosmological thinking, the existence of Grosseteste’s universe relies on a very special combination of fundamental parameters

A systematic analysis of splicing variants identifies new diagnoses in the 100,000 Genomes Project

Background Genomic variants which disrupt splicing are a major cause of rare genetic diseases. However, variants which lie outside of the canonical splice sites are difficult to interpret clinically. Improving the clinical interpretation of non-canonical splicing variants offers a major opportunity to uplift diagnostic yields from whole genome sequencing data. Methods Here, we examine the landscape of splicing variants in whole-genome sequencing data from 38,688 individuals in the 100,000 Genomes Project and assess the contribution of non-canonical splicing variants to rare genetic diseases. We use a variant-level constraint metric (the mutability-adjusted proportion of singletons) to identify constrained functional variant classes near exon–intron junctions and at putative splicing branchpoints. To identify new diagnoses for individuals with unsolved rare diseases in the 100,000 Genomes Project, we identified individuals with de novo single-nucleotide variants near exon–intron boundaries and at putative splicing branchpoints in known disease genes. We identified candidate diagnostic variants through manual phenotype matching and confirmed new molecular diagnoses through clinical variant interpretation and functional RNA studies. Results We show that near-splice positions and splicing branchpoints are highly constrained by purifying selection and harbour potentially damaging non-coding variants which are amenable to systematic analysis in sequencing data. From 258 de novo splicing variants in known rare disease genes, we identify 35 new likely diagnoses in probands with an unsolved rare disease. To date, we have confirmed a new diagnosis for six individuals, including four in whom RNA studies were performed. Conclusions Overall, we demonstrate the clinical value of examining non-canonical splicing variants in individuals with unsolved rare diseases

Sensory, computational and cognitive components of human colour constancy

When the illumination on a scene changes, so do the visual signals elicited by that scene. In spite of these changes, the objects within a scene tend to remain constant in their apparent colour. We start this review by discussing the psychophysical procedures that have been used to quantify colour constancy. The transformation imposed on the visual signals by a change in illumination dictates what the visual system must ‘undo’ to achieve constancy. The problem is mathematically underdetermined, and can be solved only by exploiting regularities of the visual world. The last decade has seen a substantial increase in our knowledge of such regularities as technical advances have made it possible to make empirical measurements of large numbers of environmental scenes and illuminants. This review provides a taxonomy of models of human colour constancy based first on the assumptions they make about how the inverse transformation might be simplified, and second, on how the parameters of the inverse transformation might be set by elements of a complex scene. Candidate algorithms for human colour constancy are represented graphically and pictorially, and the availability and utility of an accurate estimate of the illuminant is discussed. Throughout this review, we consider both the information that is, in principle, available and empirical assessments of what information the visual system actually uses. In the final section we discuss where in our visual systems these computations might be implemented

Is the S-opponent chromatic sub-system sluggish?

The S-opponent pathway has a reputation for being sluggish relative to the L/M-opponent pathway. Cottaris and De Valois [Nature 395 (1998) 896] claim that S-opponent signals are available in Macaque V1 only after 96-135 ms whereas L/M-opponent signals are available after 68-95 ms. Our experiments tested whether this large latency difference could be observed psychophysically. We measured reaction times to S/(L + M) and L/(L + M) increments. Both the equiluminant plane and the tritan line were empirically determined and we used spatio-temporal luminance noise to mask luminance cues. An adaptive staircase progressed according to observers' performance on a "go, no-go" task and provided concomitant estimates of threshold and of reaction time. When brief stimuli are confined to chromatic channels and presented at equivalent (threshold) levels and when latency is estimated from visually triggered reaction times, we find that the difference between the L/M-opponent and S-opponent sub-systems is, at most, 20-30 ms

Colour constancy in context: Roles for local adaptation and levels of reference

By determining the locations of boundaries between colour categories, we measured changes in the colour appearance of test-reflectances as a function of the simulated illumination. Test-reflectances were displayed against a variegated background of reflectance samples. Under prolonged adaptation to each illuminant, observers demonstrated a high degree of appearance-based colour constancy. By using backgrounds that consisted of chromatically biased sets of reflectances, we tested whether this stability depends on estimates of the illuminant’s cone-coordinates based on simple scene statistics. The chromatic bias of the background had only a small effect on the classification of test materials. To compare the roles of spatially local and spatially extended estimation processes, we then (unknown to the observer) simulated different illuminants on the test and on the background. Observers continued to demonstrate reasonable colour constancy. To examine the relative roles of automatic adaptation and perceptual strategies, we reduced the duration of exposure to the test compared to exposure to the background (under the conflicting illuminant). The results suggest that mechanisms that preserve information across successive test-presentations (e.g. spatially local adaptation with a time course of a few seconds, and perceptual adjustments to levels of reference) are key determinants of the stability of colour appearance

Distinct contributions to facial emotion perception of foveated vs nonfoveated facial features

Foveated stimuli receive visual processing that is quantitatively and qualitatively different from non-foveated stimuli. At normal interpersonal distances, people move their eyes around another’s face so that certain features receive foveal processing; on any given fixation, other features therefore project extrafoveally. Yet little is known about the processing of extrafoveally-presented facial features, how informative those extrafoveally-presented features are for face perception (e.g., for assessing another’s emotion), or what processes extract task-relevant (e.g., emotion-related) cues from facial features that first appear outside the fovea, and how these processes are implemented in the brain

Modulation of the face- and body-selective visual regions by the motion and emotion of point-light face and body stimuli

Neural regions selective for facial or bodily form also respond to facial or bodily motion in highly form-degraded point-light displays. Yet it is unknown whether these face-selective and body-selective regions are sensitive to human motion regardless of stimulus type (faces and bodies) or to the specific motion-related cues characteristic of their proprietary stimulus categories. Using fMRI, we show that facial and bodily motions activate selectively those populations of neurons that code for the static structure of faces and bodies. Bodily (vs. facial) motion activated body-selective EBA bilaterally and right but not left FBA, irrespective of whether observers judged the emotion or color-change in point-light angry, happy and neutral stimuli. Facial (vs. bodily) motion activated face-selective right and left FFA, but only during emotion judgments for right FFA. Moreover, the strength of responses to point-light bodies vs. faces positively correlated with voxelwise selectivity for static bodies but not faces, whereas the strength of responses to point-light faces positively correlated with voxelwise selectivity for static faces but not bodies. Emotional content carried by point-light form-from-motion cues was sufficient to enhance the activity of several regions, including bilateral EBA and right FFA and FBA. However, although the strength of emotional modulation in right and left EBA by point-light body movements was related to the degree of voxelwise selectivity to static bodies but not static faces, there was no evidence that emotional modulation in fusiform cortex occurred in a similarly stimulus category-selective manner. This latter finding strongly constrains the claim that emotionally expressive movements modulate precisely those neuronal populations that code for the viewed stimulus category

Translucence perception is not dependent on cortical areas critical for processing colour or texture

Translucence is an important property of natural materials, and human observers are adept at perceiving changes in translucence. Perceptions of different material properties appear to arise from different cortical regions, and it is therefore plausible that the perception of translucence is dependent on specialised regions, separate from those important for colour and texture processing. To test for anatomical independence between areas necessary for colour, texture and translucence perception we assessed translucency perception in a cortically colour blind observer, who performs at chance on tasks of colour and texture discrimination. Firstly, in order to establish that MS has shown no significant recovery, we assessed his colour perception performance on the Farnsworth-Munsell 100 Hue Test. Secondly, we tested him with two translucence ranking tasks. In one task, stimuli were images of glasses of tea varying in tea strength. In the other, stimuli were glasses of tea varying only in milkiness. MS was able to systematically rank both strength and milkiness, although less consistently than controls, and for tea strength his rankings were in the opposite order. An additional group of controls tested with greyscale versions of the images succeeded at the tasks, albeit slightly less consistently on the milkiness task, showing that the performance of normal observers cannot be transformed into the performance of MS simply by removing colour information from the stimuli. The systematic performance of MS suggests that some aspects of translucence perception do not depend on regions critical for colour and texture processing