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Heading estimation from optic flow relies on the assumption that the visual world is rigid. This assumption is violated when one moves through a crowd of people, a common and socially important situation. The motion of people in the crowd contains cues to their translation in the form of the articulation of their limbs, known as biological motion. We investigated how translation and articulation of biological motion influence heading estimation from optic flow for self-motion in a crowd. Participants had to estimate their heading during simulated self-motion toward a group of walkers who collectively walked in a single direction. We found that the natural combination of translation and articulation produces surprisingly small heading errors. In contrast, experimental conditions that either present only translation or only articulation produced strong idiosyncratic biases. The individual biases explained well the variance in the natural combination. A second experiment showed that the benefit of articulation and the bias produced by articulation were specific to biological motion. An analysis of the differences in biases between conditions and participants showed that different perceptual mechanisms contribute to heading perception in crowds. We suggest that coherent group motion affects the reference frame of heading perception from optic flow.

Attentional tracking and working memory tasks are often performed better when targets are divided evenly between the left and right visual hemifields, rather than contained within a single hemifield (Alvarez & Cavanagh, 2005; Delvenne, 2005). However, this bilateral field advantage does not provide conclusive evidence of hemifield-specific control of attention and working memory, as it can be explained solely from hemifield-limited spatial interference at early stages of visual processing. If control of attention and working memory is specific to each hemifield, maintaining target information should become more difficult as targets move between the two hemifields. Observers in the present study maintained targets that moved either within or between the left and right hemifields, using either attention (Experiment 1) or working memory (Experiment 2). Maintaining spatial information was more difficult when target items moved between the hemifields compared to when target items moved within their original hemifields, consistent with hemifield-specific control of spatial attention and working memory. However, this pattern was not found for maintaining identity information (e.g., color) in working memory (Experiment 3). Together, these results provide evidence that control of spatial attention and working memory is specific to each hemifield, and that hemifield-specific control is a unique signature of spatial processing.

We have recently shown that using the information carried by the mosaic of cone excitations of a stationary retina, the relative spatial contrast sensitivity function (CSF) of a computational observer has the same shape as a typical human subject. Absolute human sensitivity, however, is lower than the computational observer by a factor of 5 to 10. Here we model how additional known features of early vision affect spatial contrast sensitivity: fixational eye movements and the conversion of cone photopigment excitations to cone photocurrent responses. For a computational observer that uses a linear classifier applied to the responses of a stimulus-matched linear filter, fixational eye movements substantially change the shape of the spatial CSF, primarily by reducing sensitivity at spatial frequencies above 10 c/deg. For a computational observer that uses a translation-invariant calculation, in which decisions are based on the squared response of a quadrature-pair of linear filters, the CSF shape is little changed by eye movements, but there is a two-fold reduction in sensitivity. The noise and response dynamics of conversion of cone excitations into photocurrent introduce an additional two-fold sensitivity decrease. Hence, the combined effects of fixational eye movements and phototransduction bring the absolute sensitivity of the translation-invariant computational observer CSF to within a factor of 1 to 2 of the human CSF. We note that the human CSF depends on processing of the initial representation by many thalamic and cortical neurons, which are individually quite noisy. Our computational modeling suggests that the net effect of this noise on contrast-detection performance, when considered at the neural population level and behavioral level, is quite small: the inference mechanisms that determine the CSF, presumably in cortex, make efficient use of the information available from the cone photocurrents of the fixating eye.

Human observers are exquisitely sensitive to curvature deformations along a circular closed contour (Wilkinson, Wilson, & Habak, 1998; Hess, Wang, & Dakin, 1999; Loffler, Wilson, & Wilkinson, 2003). Such remarkable sensitivity has been attributed to the curvature encoding scheme used by V4 neurons, which typically are assumed to be equally sensitive to curvature at all polar angles (Pasupathy & Connor, 2001, 2002; Carlson, Rasquinha, Zhang, & Connor, 2011). To test the assumption that detection thresholds for curvature deformations are invariant across polar angles, we used a novel stimulus class we call Difference of Gaussian (DoG) contours that allowed us to independently manipulate the amplitude, angular frequency, and polar angle of curvature of a closed-contour shape while measuring contour-curvature thresholds. Our results demonstrate that (a) detection thresholds were higher when observers were uncertain about the location of the curvature deformation, but on average, thresholds did not vary significantly across 24 polar angles; (b) the direction and magnitude of the oblique effect varies across individuals; (c) there is a strong association between detecting a contour deformation and identifying its location; (d) curvature detectors may serve as labeled lines.

The contrast sensitivity function (CSF) is an informative measure of visual health, but the practical difficulty of measuring it has impeded detailed analyses of its relationship to different visual disorders. Furthermore, most existing tasks cannot be used in populations with cognitive impairment. We analyzed detailed CSFs measured with a nonverbal procedure called "Gradiate," which efficiently infers visibility from eye movements and manipulates stimulus appearance in real time. Sixty observers of varying age (38 with refractive error) were presented with moving stimuli. Stimulus spatial frequency and contrast advanced along 15 radial sweeps through CSF space in response to stimulus-congruent eye movements. A point on the CSF was recorded when tracking ceased. Gradiate CSFs were reliable and in high agreement with independent low-contrast acuity thresholds. Overall CSF variation was largely captured by two orthogonal factors ("radius" and "slope") or two orthogonal shape factors when size was normalized ("aspect ratio" and "curvature"). CSF radius was highly predictive of LogMAR acuity, as were aspect ratio and curvature together, but only radius was predictive of observer age. Our findings suggest that Gradiate holds promise for assessing spatial vision in both verbal and nonverbal populations and indicate that variation between detailed CSFs can reveal useful information about visual health.

Although the contrast sensitivity function (CSF) changes markedly during infancy, there is no consensus regarding whether, how, and why it continues to develop in later childhood. Here, we analyzed previously published data (N = 1928 CSFs), and present new psychophysical findings from 98 children (4.7–14.8 years) and 50 adults (18.1–29.7 years), in order to answer the following questions: (1) Does the CSF change during childhood? (2) How large is the developmental effect size? (3) Are any changes uniform across the CSF, or frequency-specific? and (4) Can some or all of the changes be explained by “non-visual” (i.e. procedural/cognitive) factors, such as boredom or inattentiveness? The new data were collected using a four-alternative forced-choice (4AFC) Gabor-detection task, with two different psychophysical procedures (Weighted Staircase; QUEST+), and suprathreshold (false-negative) catch trials to quantify lapse rates. It is shown that from ages 4 to 18 years, the CSF improves (at an exponentially decaying rate) by approximately 0.3 log10 units (a doubling of contrast sensitivity [CS]), with 90% of this change complete by 12 years of age. The size of the effect was small relative to individual variability, with age alone explaining less than one sixth of variability (16%), and most children performing as well as some adults (i.e. falling within the 90% population limits for adults). Development was frequency-specific, with changes occurring primarily around or below the CSF peak (≤ 4 cpd). At least half — and potentially all — of the changes observed could be explained by non-visual factors (e.g. lapses in concentration), although possible biological mechanisms are discussed.

Interpreting colormap visualizations requires determining how dimensions of color in visualizations map onto quantities in data. People have color-based biases that influence their interpretations of colormaps, such as a dark-is-more bias-darker colors map to larger quantities. Previous studies of color-based biases focused on colormaps with weak data spatial structure, but color-based biases may not generalize to colormaps with strong data spatial structure, like "hotspots" typically found in weather maps and neuroimaging brain maps. There may be a hotspot-is-more bias to infer that colors within hotspots represent larger quantities, which may override the dark-is-more bias. We tested this possibility in four experiments. Participants saw colormaps with hotspots and a legend that specified the color-quantity mapping. Their task was to indicate which side of the colormap depicted larger quantities (left/right). We varied whether the legend specified dark-more mapping or light-more mapping across trials and operationalized a dark-is-more bias as faster response time (RT) when the legend specified dark-more mapping. Experiment 1 demonstrated robust evidence for the dark-is-more bias, without evidence for a hotspot-is-more bias. Experiments 2 to 4 suggest that a hotspot-is-more bias becomes relevant when hotspots are a statistically reliable cue to "more" (i.e., the locus of larger quantities) and when hotspots are more perceptually pronounced. Yet, comparing conditions in which the hotspots were "more," RTs were always faster for dark hotspots than light hotspots. Thus, in the presence of strong spatial cues to the locus of larger quantities, color-based biases still influenced interpretations of colormap data visualizations.

Whenever we move our eyes, some visual information obtained before a saccade is combined with the visual information obtained after a saccade. Interestingly, saccades rarely land exactly on the saccade target, which may pose a problem for transsaccadic perception as it could affect the quality of postsaccadic input. Recently, however, we showed that transsaccadic feature integration is actually unaffected by deviations of saccade landing points. Possibly, transsaccadic integration remains unaffected because the presaccadic shift of attention follows the intended saccade target and not the actual saccade landing point during regular saccades. Here, we investigated whether saccade landing point errors can in fact alter transsaccadic perception when the presaccadic shift of attention follows the saccade landing point deviation. Given that saccadic adaptation not only changes the saccade vector, but also the presaccadic shift of attention, we combined a feature report paradigm with saccadic adaptation. Observers reported the color of the saccade target, which occasionally changed slightly during a saccade to the target. This task was performed before and after saccadic adaptation. The results showed that, after adaptation, presaccadic color information became less precise and transsaccadic perception had a stronger reliance on the postsaccadic color estimate. Therefore, although previous studies have shown that transsaccadic perception is generally unaffected by saccade landing point deviations, our results reveal that this cannot be considered a general property of the visual system. When presaccadic shifts of attention follow altered saccade landing points, transsaccadic perception is affected, suggesting that transsaccadic feature perception might be dependent on visual spatial attention.

A normally sighted person can see a grating of 30 cycles per degree or higher, but spatial frequencies needed for motion perception are much lower than that. It is unknown for natural images with a wide spectrum how all the visible spatial frequencies contribute to motion speed perception. In this work, we studied the effect of spatial frequency content on motion speed estimation for sequences of natural and stochastic pixel images by simulating different visual conditions, including normal vision, low vision (low-pass filtering), and complementary vision (high-pass filtering at the same cutoff frequencies of the corresponding low-vision conditions) conditions. Speed was computed using a biological motion energy-based computational model. In natural sequences, there was no difference in speed estimation error between normal vision and low vision conditions, but it was significantly higher for complementary vision conditions (containing only high-frequency components) at higher speeds. In stochastic sequences that had a flat frequency distribution, the error in normal vision condition was significantly larger compared with low vision conditions at high speeds. On the contrary, such a detrimental effect on speed estimation accuracy was not found for low spatial frequencies. The simulation results were consistent with the motion direction detection task performed by human observers viewing stochastic sequences. Together, these results (i) reiterate the importance of low frequencies in motion perception, and (ii) indicate that high frequencies may be detrimental for speed estimation when low frequency content is weak or not present.

The sudden appearance of an unexpected object elicits the automatic allocation of spatial attention. Even without eye movements, effortless, but transient, improvements in perception occur at the onset location. Much is known about the consequences of such exogenously elicited shifts of covert attention, but most research has used stimuli that carry very little, if any, additional information. In everyday life, attention is captured by sudden onsets that, due to past experience, alert us to more than just their appearance. An abundance of recent work has shed light on the interaction of associative learning and attention, leading to refinements in current models of attentional control; in this study, we tested two hypotheses concerning the efficacy of meaning-imbued onsets, specifically those that predict reward, to drive the reflexive allocation of covert spatial attention and to improve task performance more generally. First, spatially uninformative, abrupt-onset cues that are predictive of reward may elicit the involuntary allocation of attention more effectively than nonreward-predictive onsets; second, the presence of peripheral cues that are predictive of reward, regardless of validity, may impact global attentional processes in a spatially nonspecific manner. We paired monetary reward with one of two luminance-defined, abrupt-onset cues and measured each cue's ability to modulate performance in a visual task. Replicating research with nonmeaning-imbued stimuli, both kinds of abrupt onsets reflexively improved visual perception at attended, relative to unattended, locations. However, when features of the onset predicted the availability of monetary reward, enhancements in perception become less constrained, spreading rapidly to other task-relevant locations.

A central question in vision is whether spatial attention is represented in an eye-centered (retinotopic) or world-centered (spatiotopic) reference-frame. Most previous studies on this question focused on how coordinates are modulated across saccades. In the present study, we investigated the reference-frame of attention across smooth pursuit eye-movements using a goal-directed saccade task. In two experiments, participants were asked to pursue a moving target while attending to one or two grating stimuli. On each trial, one stimulus was constant in its retinal position and the other was constant in its spatial position. Upon detection of a slight change in stimulus orientation, participants were asked to stop pursuing and perform a fast saccade toward the modified stimulus. In the focused attention condition, they attended one, predefined, stimulus, and in the divided attention condition they attended both. In Experiment 1 the angle of the orientation change marking the target event was constant across participants and conditions. In Experiment 2, the angle was individually adapted to equate performance across participants and conditions. Findings of the two experiments were consistent and showed that the enhancement of mean visual sensitivity in the focused relative to the divided attention condition was similar in magnitude for both retinotopic and spatiotopic targets. This indicates that during smooth pursuit, endogenous attention was proportionally divided between targets in retinotopic and spatiotopic frames of reference.

How do we explore the visual environment around us, and how are head and eye movements coordinated during our exploration? To investigate this question, we had observers look at omnidirectional panoramic scenes, composed of both landscape and fractal images, using a virtual reality viewer while their eye and head movements were tracked. We analyzed the spatial distribution of eye fixations and the distribution of saccade directions and the spatial distribution of head positions and the distribution of head shifts, as well as the relation between eye and head movements. The results show that, for landscape scenes, eye and head behavior best fit the allocentric frame defined by the scene horizon, especially when head tilt (i.e., head rotation around the view axis) is considered. For fractal scenes, which have an isotropic texture, eye and head movements were executed primarily along the cardinal directions in world coordinates. The results also show that eye and head movements are closely linked in space and time in a complementary way, with stimulus-driven eye movements predominantly leading the head movements. Our study is the first to systematically examine eye and head movements in a panoramic virtual reality environment, and the results demonstrate that a virtual reality environment constitutes a powerful and informative research alternative to traditional methods for investigating looking behavior.

Top-down visual attention selectively filters sensory input so relevant information receives preferential processing. Feature-based attention (FBA) enhances the representation of relevant low-level features, whereas space-based attention (SBA) enhances information at relevant location(s). The present study investigates whether the unique influences of SBA and FBA combine to facilitate behavior in a perceptually demanding discrimination task. We first demonstrated that, independently, both color and location pre-cues could effectively direct attention to facilitate perceptual decision making of a target. We then examined the combined effects of SBA and FBA in the same design by deploying a predictive color arrow pre-cue. Only SBA effects were observed in performance accuracy and reaction time. However, we detected a reaction time cost when a valid spatial cue was paired with a feature cue. A computational perceptual decision-making model largely provided converging evidence that contributions from FBA were restricted to facilitating the speed with which the relevant item was identified. Our results suggest that both selection mechanisms can be used in isolation to resolve a perceptually challenging target in a sparse display, but with little additive perceptual benefit when cued simultaneously. We conclude that there is at least some higher order interdependence between space-based and feature-based selection during decision making under specific conditions.

Amblyopia is a cortical visual disorder caused by unequal visual input to the brain from the two eyes during development. Amblyopes show reduced visual acuity and contrast sensitivity and abnormal binocularity, as well as more "global" perceptual losses, such as figure-ground segregation and global form integration. Currently, there is no consensus on the neural basis for these higher-order perceptual losses. One contributing factor could be that amblyopes have deficiencies in attention, such that the attentional processes that control the selection of information favor the better eye. Previous studies in amblyopic adults are conflicting as to whether attentional deficits exist. However, studies where intact attentional ability has been shown to exist were conducted in adults; it is possible that it was acquired through experience. To test this hypothesis, we studied attentional processing in amblyopic children. We examined covert endogenous attention using a classical spatial cueing paradigm in amblyopic and visually typical 5- to 10-year old children. We found that all children, like adults, independently of visual condition, benefited from attentional cueing: They performed significantly better on trials with an informative (valid) cue than with the uninformative (neutral) cue. Response latencies were also significantly shorter for the valid cue condition. No statistically significant difference was found between the performance of the amblyopic and the visually typical children or between dominant and nondominant eyes of all children. The results showed that covert spatial attention is intact in amblyopic and visually typical children and is therefore not likely to account for higher-order perceptual losses in amblyopic children.

Spatial frequency (SF) information is essential for visual perception. By combining a sensitization procedure and the Ebbinghaus illusion, we investigated the effect of SF bias in context-dependent visual size perception. During the sensitization phase, participants were repeatedly presented with low- or high-pass filtered faces or gratings and were asked to discriminate the gender or the orientation of them, respectively. Immediately following the sensitization phase, the Ebbinghaus illusion strength was measured. The results showed that the illusion strength was significantly larger when the prior sensitized images were low-pass filtered relative to when they were high-pass filtered. Moreover, this SF bias was independent of low-level features and the specific content of the filtered images. Our findings extend the understanding of SF bias induced by sensitization in visual domain, and suggest that the processing of context-dependent visual size information is likely to involve magnocellular projections from subcortical areas via low SF channel.

Photographs and line drawings of natural scenes are easily classified even when the image is only briefly visible to the observer. Contour junctions and points of high curvature have been shown to be important for perceptual organization (Attneave, 1954; Biederman, 1987) and have been proposed to be influential in rapid scene classification (Walther & Shen, 2014). Here, we manipulate the junctions in images, either randomly translating them, or selectively removing or maintaining them. Observers were better at classifying images when the contours were randomly translated (disrupting the junctions) than when the junctions were randomly shifted (partially disrupting contour information). Moreover, observers were better at classifying a scene when shown only segments between junctions, than when shown only the junctions, with the middle segments removed. These results suggest that categorizing line drawings of real-world scenes does not solely rely on junction statistics. The spatial locations of the junctions are important, as well as their relationships with one another. Furthermore, the segments between junctions appear to facilitate scene classification, possibly due to their involvement in symmetry relationships with other contour segments.

In the time leading up to a saccade, the saccade target is perceptually enhanced compared to other objects in the visual field. This enhancement is attributed to a shift of spatial attention toward the target. We examined whether the presence of visual objects is critical for the perceptual enhancement at the saccade target to occur. We hypothesized that attention may need an object to focus on in order to be effective. We conducted four experiments using a dual-task design, where participants performed eye movements either to a location demarked by a placeholder or to an empty screen location where no object was displayed. At the same time, they discriminated a probe flashed at the location targeted by the eye movement or at one of two control locations. A strong perceptual advantage at the saccade target location was observed only when placeholders were displayed at the time of probe presentation. The complete absence of placeholders (Experiment 1), the presence of placeholders before but not during probe presentation (Experiment 3), and the presence of objects only around the saccade target (Experiments 3 and 4) led to a strong reduction in the saccade-target benefit. We conclude that placeholders may indeed be necessary to observe presaccadic enhancement at the saccade target. However, this is not because placeholders provide an object to focus attention on, but rather because they produce a masking (or crowding) effect. This detrimental effect is overcome by the presaccadic shift of attention, resulting in heightened perception only at the saccade target object.

The study of how visual processing functions in the absence of visual awareness has become a major research interest in the vision-science community. One of the main sources of evidence that stimuli that do not reach conscious awareness-and are thus "invisible"-are still processed to some degree by the visual system comes from studies using continuous flash suppression (CFS). Why and how CFS works may provide more general insight into how stimuli access awareness. As spatial and temporal properties of stimuli are major determinants of visual perception, we hypothesized that these properties of the CFS masks would be of significant importance to the achieved suppression depth. In previous studies however, the spatial and temporal properties of the masks themselves have received little study, and masking parameters vary widely across studies, making a metacomparison difficult. To investigate the factors that determine the effectiveness of CFS, we varied both the temporal frequency and the spatial density of Mondrian-style masks. We consistently found the longest suppression duration for a mask temporal frequency of around 6 Hz. In trials using masks with reduced spatial density, suppression was weaker and frequency tuning was less precise. In contrast, removing color reduced mask effectiveness but did not change the pattern of suppression strength as a function of frequency. Overall, this pattern of results stresses the importance of CFS mask parameters and is consistent with the idea that CFS works by disrupting the spatiotemporal mechanisms that underlie conscious access to visual input.

Are people biologically prepared for the rapid detection of threat posed by an angry facial expression, even when it is conveyed in the form of a schematic line drawing? Based on visual search times, the current literature would suggest that the answer is yes. But are there low-level explanations for this effect? Here, we present visual search results for schematic faces using current best practice, based on a concentric search array and set size manipulation. Using this approach, we replicate the classic search advantage for angry over happy faces. However, we also report a comparable effect when abstract plus- and square-shaped stimuli-derived from the angry and happy schematic faces respectively-are used within the same paradigm. We then go on to demonstrate that, while reduced, the effect remains after removal of the circular surround, bringing us closer to the source of the effect. We explore the possibility that the source of this search asymmetry could be the iso-feature suppression and collinear facilitation model proposed in Li's (1999a, 1999b, and 2002) bottom-up model of saliency. Simulations with this model using the abstract stimuli align with the corresponding behavioral results (i.e., the plus shape was found to be more salient than the square). Given the deliberate similarities between these abstract shapes and the respective face stimuli, we propose that the underlying cause for the asymmetries typically found using schematic faces, may be more related to early visual processing of line orientation than threat detection.

We almost never experience visual instability, despite retinal image instability induced by eye movements. How the stability of visual perception is maintained through spatiotopic representation remains a matter of debate. The discrepancies observed in the findings of existing neuroscience studies regarding spatiotopic representation partly originate from differences in regard to how attention is deployed to stimuli. In this study, we psychophysically examined whether spatial attention is needed to perceive spatiotopic visual motion. For this purpose, we used visual motion priming, which is a phenomenon in which a preceding priming stimulus modulates the perceived moving direction of an ambiguous test stimulus, such as a drifting grating that phase shifts by 180°. To examine the priming effect in different coordinates, participants performed a saccade soon after the offset of a primer. The participants were tasked with judging the direction of a subsequently presented test stimulus. To control the effect of spatial attention, the participants were asked to conduct a concurrent dot contrast-change detection task after the saccade. Positive priming was prominent in spatiotopic conditions, whereas negative priming was dominant in retinotopic conditions. At least a 600-ms interval between the priming and test stimuli was needed to observe positive priming in spatiotopic coordinates. When spatial attention was directed away from the location of the test stimulus, spatiotopic positive motion priming completely disappeared; meanwhile, the spatiotopic positive motion priming at shorter interstimulus intervals was enhanced when spatial attention was directed to the location of the test stimulus. These results provide evidence that an attentional resource is requisite for developing spatiotopic representation more quickly.

Effective gaze control in traffic, based on peripheral visual information, is important to avoid hazards. Whereas previous hazard perception research mainly focused on skill-component development (e.g., orientation and hazard processing), little is known about the role and dynamics of peripheral vision in hazard perception. We analyzed eye movement data from a study in which participants scanned static traffic scenes including medium-level versus dangerous hazards and focused on characteristics of fixations prior to entering the hazard region. We found that initial saccade amplitudes into the hazard region were substantially longer for dangerous (vs. medium-level) hazards, irrespective of participants' driving expertise. An analysis of the temporal dynamics of this hazard-level dependent saccade targeting distance effect revealed that peripheral hazard-level processing occurred around 200-400 ms during the course of the fixation prior to entering the hazard region. An additional psychophysical hazard detection experiment, in which hazard eccentricity was manipulated, revealed better detection for dangerous (vs. medium-level) hazards in both central and peripheral vision. Furthermore, we observed a significant perceptual decline from center to periphery for medium (but not for highly) dangerous hazards. Overall, the results suggest that hazard processing is remarkably effective in peripheral vision and utilized to guide the eyes toward potential hazards.

Ensemble coding supports rapid extraction of visual statistics about distributed visual information. Researchers typically study this ability with the goal of drawing conclusions about how such coding extracts information from natural scenes. Here we argue that a second domain can serve as another strong inspiration for understanding ensemble coding: graphs, maps, and other visual presentations of data. Data visualizations allow observers to leverage their ability to perform visual ensemble statistics on distributions of spatial or featural visual information to estimate actual statistics on data. We survey the types of visual statistical tasks that occur within data visualizations across everyday examples, such as scatterplots, and more specialized images, such as weather maps or depictions of patterns in text. We divide these tasks into four categories: identification of sets of values, summarization across those values, segmentation of collections, and estimation of structure. We point to unanswered questions for each category and give examples of such cross-pollination in the current literature. Increased collaboration between the data visualization and perceptual psychology research communities can inspire new solutions to challenges in visualization while simultaneously exposing unsolved problems in perception research.

Enhanced spatial processing of local visual details has been reported in individuals with autism spectrum conditions (ASC), and crowding is postulated to be a mechanism that may produce this ability. However, evidence for atypical crowding in ASC is mixed, with some studies reporting a complete lack of crowding in autism and others reporting a typical magnitude of crowding between individuals with and without ASC. Here, we aim to disambiguate these conflicting results by testing both the magnitude and the spatial extent of crowding in individuals with ASC (N = 25) and age- and IQ-matched controls (N = 23) during an orientation discrimination task. We find a strong crowding effect in individuals with and without ASC, which falls off as the distance between target and flanker is increased. Both the magnitude and the spatial range of this effect were comparable between individuals with and without ASC. We also find typical (uncrowded) orientation discrimination thresholds in individuals with ASC. These findings suggest that the spatial extent of crowding is unremarkable in ASC, and is therefore unlikely to account for the visual symptoms reported in individuals with the diagnosis.

Multiple methods exist for measuring how age influences the rate of visual information processing. The most advanced methods model the processing dynamics in a task in order to estimate processing rates independently of other factors that might be influenced by age, such as overall performance level and the time at which processing onsets. However, such modeling techniques have produced mixed evidence for age effects. Using a time-accuracy function (TAF) analysis, Kliegl, Mayr, and Krampe (1994) showed clear evidence for age effects on processing rate. In contrast, using the diffusion model to examine the dynamics of decision processes, Ratcliff and colleagues (e.g., Ratcliff, Thapar, & McKoon, 2006) found no evidence for age effects on processing rate across a range of tasks. Examination of these studies suggests that the number of display stimuli might account for the different findings. In three experiments we measured the precision of younger and older adults' representations of target stimuli after different amounts of stimulus exposure. A TAF analysis found little evidence for age differences in processing rate when a single stimulus was presented (Experiment 1). However, adding three nontargets to the display resulted in age-related slowing of processing (Experiment 2). Similar slowing was observed when simply presenting two stimuli and using a post-cue to indicate the target (Experiment 3). Although there was some interference from distracting objects and from previous responses, these age-related effects on processing rate seem to reflect an age-related difficulty in processing multiple objects, particularly when encoding them into visual working memory.

Distinct attentional mechanisms enhance the sensory processing of visual stimuli that appear at task-relevant locations and have task-relevant features. We used a combination of psychophysics and computational modeling to investigate how these two types of attention--spatial and feature based--interact to modulate sensitivity when combined in one task. Observers monitored overlapping groups of dots for a target change in color saturation, which they had to localize as being in the upper or lower visual hemifield. Pre-cues indicated the target's most likely location (left/right), color (red/green), or both location and color. We measured sensitivity (d') for every combination of the location cue and the color cue, each of which could be valid, neutral, or invalid. When three competing saturation changes occurred simultaneously with the target change, there was a clear interaction: The spatial cueing effect was strongest for the cued color, and the color cueing effect was strongest at the cued location. In a second experiment, only the target dot group changed saturation, such that stimulus competition was low. The resulting cueing effects were statistically independent and additive: The color cueing effect was equally strong at attended and unattended locations. We account for these data with a computational model in which spatial and feature-based attention independently modulate the gain of sensory responses, consistent with measurements of cortical activity. Multiple responses then compete via divisive normalization. Sufficient competition creates interactions between the two cueing effects, although the attentional systems are themselves independent. This model helps reconcile seemingly disparate behavioral and physiological findings.

Psychophysical inferences about the neural mechanisms supporting spatial vision can be undermined by uncertainties introduced by optical aberrations and fixational eye movements, particularly in fovea where the neuronal grain of the visual system is fine. We examined the effect of these preneural factors on photopic spatial summation in the human fovea using a custom adaptive optics scanning light ophthalmoscope that provided control over optical aberrations and retinal stimulus motion. Consistent with previous results, Ricco's area of complete summation encompassed multiple photoreceptors when measured with ordinary amounts of ocular aberrations and retinal stimulus motion. When both factors were minimized experimentally, summation areas were essentially unchanged, suggesting that foveal spatial summation is limited by postreceptoral neural pooling. We compared our behavioral data to predictions generated with a physiologically-inspired front-end model of the visual system, and were able to capture the shape of the summation curves obtained with and without pre-retinal factors using a single postreceptoral summing filter of fixed spatial extent. Given our data and modeling, neurons in the magnocellular visual pathway, such as parasol ganglion cells, provide a candidate neural correlate of Ricco's area in the central fovea.

Endogenous and exogenous visuospatial attention both alter spatial resolution, but they operate via distinct mechanisms. In texture segmentation tasks, exogenous attention inflexibly increases resolution even when detrimental for the task at hand and does so by modulating second-order processing. Endogenous attention is more flexible and modulates resolution to benefit performance according to task demands, but it is unknown whether it also operates at the second-order level. To answer this question, we measured performance on a second-order texture segmentation task while independently manipulating endogenous and exogenous attention. Observers discriminated a second-order texture target at several eccentricities. We found that endogenous attention improved performance uniformly across eccentricity, suggesting a flexible mechanism that can increase or decrease resolution based on task demands. In contrast, exogenous attention improved performance in the periphery but impaired it at central retinal locations, consistent with an inflexible resolution enhancement. Our results reveal that endogenous and exogenous attention both alter spatial resolution by differentially modulating second-order processing.

It has recently been shown that adapting to a densely textured stimulus alters the perception of visual space, such that the distance between two points subsequently presented in the adapted region appears reduced (Hisakata, Nishida, & Johnston, 2016). We asked whether this form of adaptation-induced spatial compression alters visual crowding. To address this question, we first adapted observers to a dynamic dot texture presented within an annular region surrounding the test location. Following adaptation, observers perceived a test array comprised of multiple oriented dot dipoles as spatially compressed, resulting in an overall reduction in perceived size. We then tested to what extent this spatial compression influences crowding by measuring orientation discrimination of a single dipole flanked by randomly oriented dipoles across a range of separations. Following adaptation, we found that the magnitude of crowding was predicted by the physical rather than perceptual separation between center and flanking dipoles. These findings contrast with previous studies in which crowding has been shown to increase when motion-induced position shifts act to reduce apparent separation (Dakin, Greenwood, Carlson, & Bex, 2011; Maus, Fischer, & Whitney, 2011).

Amblyopia, a developmental disorder of vision, affects many aspects of spatial vision as well as motion perception and some cognitive skills. Current models of amblyopic vision based on known neurophysiological deficiencies have yet to provide an understanding of the wide range of amblyopic perceptual losses. Visual spatial attention is known to enhance performance in a variety of detection and discrimination tasks in visually typical humans and nonhuman primates. We investigated whether and how voluntary spatial attention affected psychophysical performance in amblyopic macaques. Full-contrast response functions for motion direction discrimination were measured for each eye of six monkeys: five amblyopic and one control. We assessed whether the effect of a valid spatial cue on performance corresponded to a change in contrast gain, a leftward shift of the function, or response gain, an upward scaling of the function. Our results showed that macaque amblyopes benefit from a valid spatial cue. Performance with amblyopic eyes viewing showed enhancement of both contrast and response gain whereas fellow and control eyes' performance showed only contrast gain. Reaction time analysis showed no speed accuracy trade-off in any case. The valid spatial cue improved contrast sensitivity for the amblyopic eye, effectively eliminating the amblyopic contrast sensitivity deficit. These results suggest that engaging endogenous spatial attention may confer substantial benefit to amblyopic vision.

Visual blur is a common problem that causes difficulty in pattern recognition for normally sighted people under degraded viewing conditions (e.g., near the acuity limit, when defocused, or in fog) and also for people with impaired vision. For reliable identification, the spatial frequency content of an object needs to extend up to or exceed a minimum value in units of cycles per object, referred to as the critical spatial frequency. In this study, we investigated the critical spatial frequency for alphabet and Chinese characters, and examined the effect of pattern complexity. The stimuli were divided into seven categories based on their perimetric complexity, including the lowercase and uppercase alphabet letters, and five groups of Chinese characters. We found that the critical spatial frequency significantly increased with complexity, from 1.01 cycles per character for the simplest group to 2.00 cycles per character for the most complex group of Chinese characters. A second goal of the study was to test a space-bandwidth invariance hypothesis that would represent a tradeoff between the critical spatial frequency and the number of adjacent patterns that can be recognized at one time. We tested this hypothesis by comparing the critical spatial frequencies in cycles per character from the current study and visual-span sizes in number of characters (measured by Wang, He, & Legge, 2014) for sets of characters with different complexities. For the character size (1.2°) we used in the study, we found an invariant product of approximately 10 cycles, which may represent a capacity limitation on visual pattern recognition.

The oblique effect-poorer performance when contours are in oblique meridians-is here extended from the discrimination of line-orientation to the tilt illusion and to the detection and contextual induction of curvature. The distinction is made between a contour's susceptibility to contextual perturbation and its capacity to induce such perturbation, for which the oblique effect is only about one half. That the cardinal/oblique superiority is retained for the orientation of illusory borders and for the implicit orientation of shapes lacking explicit rectilinear delineation has implications for its neural substrate. To the extent that a geometrical-visual illusion, such as Poggendorff's or Hering's, depends on interaction in the domain of contour orientation, it manifests a corresponding orientational anisotropy. On the other hand, visual functions that govern whether and how well a boundary is visible are invariant with orientation.

Retinal topography maps are a widely used tool in vision science, neuroscience, and visual ecology, providing an informative visualization of the spatial distribution of cell densities across the retinal hemisphere. Here, we introduce Retina, an R package for computational mapping, inspection of topographic model fits, and generation of average maps. Functions in Retina take cell count data obtained from retinal wholemounts using stereology software. Accurate visualizations and comparisons between different eyes have been difficult in the past, because of deformation and incisions of retinal wholemounts. We account for these issues by incorporation of the R package Retistruct, which results in a retrodeformation of the wholemount into a hemispherical shape, similar to the original eyecup. The maps are generated by thin plate splines, after the data were transformed into a two-dimensional space with an azimuthal equidistant plot projection. Retina users can compute retinal topography maps independent of stereology software choice and assess model fits with a variety of diagnostic plots. Functionality of Retina also includes species average maps, an essential feature for interspecific analyses. The Retina package will facilitate rigorous comparative studies in visual ecology by providing a robust quantitative approach to generate retinal topography maps.

Several physiological studies in cats and monkeys have reported that the spatial frequency (SF) tuning of visual neurons varies depending on the luminance contrast and size of stimulus. However, comparatively little is known about the effect of changing the stimulus contrast and size on SF tuning in human perception. In the present study, we investigated the effects of stimulus size and luminance contrast on human SF tuning using the subspace-reverse-correlation method. Measuring SF tunings at six different stimulus sizes and three different luminance contrast conditions (90%, 10%, and 1%), we found that human perception exhibits significant stimulus-size-dependent SF tunings. At 90% and 10% contrast, participants exhibited relative SF tuning (cycles/image) rather than absolute SF tuning (cycles/°) at response peak latency. On the other hand, at 1% contrast, the magnitude of the size-dependent-peak SF shift was too small for strictly relative SF tuning. These results show that human SF tuning is not fixed, but varies depending on the stimulus size and contrast. This dependency may contribute to size-invariant object recognition within an appropriate contrast rage.

The contrast sensitivity function (CSF), a measure of visual sensitivity to a wide range of spatial frequencies, has been widely used as the gain profile of the front-end filter of the visual system to predict how we perceive spatial patterns. However, the CSF itself is determined by the gain profile and other processing inefficiencies of the visual system; it may be problematic to use the CSF as the gain profile in observer models. Here, we applied the external noise paradigm and the perceptual template model (PTM) to characterize several major properties of the visual system. With the external noise normalized gain profile, nonlinearity, and internal additive and multiplicative noises, the PTM accounted for 92.8% of the variance in the experiment data measured in a wide range of conditions and revealed the major processing components that determine the CSF. Unlike the CSF, the external noise normalized gain profile of the visual system is relatively flat across a wide range of spatial frequencies. The results may have major implications for understanding normal and abnormal spatial vision.

Our visual system allows us to localize objects in the world and plan motor actions toward them. We have recently shown that the localization of moving objects differs between perception and saccadic eye movements (Lisi & Cavanagh, 2015), suggesting different localization mechanisms for perception and action. This finding, however, could reflect a unique feature of the saccade system rather than a general dissociation between perception and action. To disentangle these hypotheses, we compared object localization between saccades and hand movements. We flashed brief targets on top of double-drift stimuli (moving Gabors with the internal pattern drifting orthogonally to their displacement, inducing large distortions in perceived location and direction) and asked participants to point or make saccades to them. We found a surprising difference between the two types of movements: Although saccades targeted the physical location of the flashes, pointing movements were strongly biased toward the perceived location (about 63% of the perceptual illusion). The same bias was found when pointing movements were made in open-loop conditions (without vision of the hand). These results indicate that dissociations are present between different types of actions (not only between action and perception) and that visual processing for saccadic eye movements differs from that for other actions. Because the position bias in the double-drift stimulus depends on a persisting influence of past sensory signals, we suggest that spatial maps for saccades might reflect only recent, short-lived signals, and the spatial representations supporting conscious perception and hand movements integrate visual input over longer temporal intervals.

Certain abnormalities in behavioral performance and neural signaling have been attributed to a deficit of visual attention in amblyopia, a neurodevelopmental disorder characterized by a diverse array of visual deficits following abnormal binocular childhood experience. Critically, most have inferred attention's role in their task without explicitly manipulating and measuring its effects against a baseline condition. Here, we directly investigate whether human amblyopic adults benefit from covert spatial attention-the selective processing of visual information in the absence of eye movements-to the same degree as neurotypical observers. We manipulated both involuntary (Experiment 1) and voluntary (Experiment 2) attention during an orientation discrimination task for which the effects of covert spatial attention have been well established in neurotypical and special populations. In both experiments, attention significantly improved accuracy and decreased reaction times to a similar extent (a) between the eyes of the amblyopic adults and (b) between the amblyopes and their age- and gender-matched controls. Moreover, deployment of voluntary attention away from the target location significantly impaired task performance (Experiment 2). The magnitudes of the involuntary and voluntary attention benefits did not correlate with amblyopic depth or severity. Both groups of observers showed canonical performance fields (better performance along the horizontal than vertical meridian and at the lower than upper vertical meridian) and similar effects of attention across locations. Despite their characteristic low-level vision impairments, covert spatial attention remains functionally intact in human amblyopic adults.

Spatial selectivity, as measured by functional magnetic resonance imaging (fMRI) activity patterns that vary consistently with the location of visual stimuli, has been documented in many human brain regions, notably the occipital visual cortex and the frontal and parietal regions that are active during endogenous, goal-directed attention. We hypothesized that spatial selectivity also exists in regions that are active during exogenous, stimulus-driven attention. To test this hypothesis, we acquired fMRI data while subjects maintained passive fixation. At jittered time intervals, a briefly presented wedge-shaped array of rapidly expanding circles appeared at one of three contralateral or one of three ipsilateral locations. Positive fMRI activations were identified in multiple brain regions commonly associated with exogenous attention, including the temporoparietal junction, the inferior parietal lobule, and the inferior frontal sulcus. These activations were not organized as a map across the cortical surface. However, multivoxel pattern analysis of the fMRI activity correctly classified every pair of stimulus locations, demonstrating that patterns of fMRI activity were correlated with spatial location. These observations held for both contralateral and ipsilateral stimulus pairs as well as for stimuli of different textures (radial checkerboard) and shapes (squares and rings). Permutation testing verified that the obtained accuracies were not due to systematic biases and demonstrated that the findings were statistically significant.

Behavioral research has demonstrated that the shape and texture of single objects can be processed independently. Similarly, neuroimaging results have shown that an object's shape and texture are processed in distinct brain regions with shape in the lateral occipital area and texture in parahippocampal cortex. Meanwhile, objects are not always seen in isolation and are often grouped together as an ensemble. We recently showed that the processing of ensembles also involves parahippocampal cortex and that the shape and texture of ensemble elements are processed together within this region. These neural data suggest that the independence seen between shape and texture in single-object perception would not be observed in object-ensemble perception. Here we tested this prediction by examining whether observers could attend to the shape of ensemble elements while ignoring changes in an unattended texture feature and vice versa. Across six behavioral experiments, we replicated previous findings of independence between shape and texture in single-object perception. In contrast, we observed that changes in an unattended ensemble feature negatively impacted the processing of an attended ensemble feature only when ensemble features were attended globally. When they were attended locally, thereby making ensemble processing similar to single-object processing, interference was abolished. Overall, these findings confirm previous neuroimaging results and suggest that distinct cognitive mechanisms may be involved in single-object and object-ensemble perception. Additionally, they show that the scope of visual attention plays a critical role in determining which type of object processing (ensemble or single object) is engaged by the visual system.

The simultaneous-sequential method was used to test the processing capacity of statistical summary representations both within and between feature dimensions. Sixteen gratings varied with respect to their size and orientation. In Experiment 1, the gratings were equally divided into four separate smaller sets, one of which with a mean size that was larger or smaller than the other three sets, and one of which with a mean orientation that was tilted more leftward or rightward. The task was to report the mean size and orientation of the oddball sets. This therefore required four summary representations for size and another four for orientation. The sets were presented at the same time in the simultaneous condition or across two temporal frames in the sequential condition. Experiment 1 showed evidence of a sequential advantage, suggesting that the system may be limited with respect to establishing multiple within-feature summaries. Experiment 2 eliminates the possibility that some aspect of the task, other than averaging, was contributing to this observed limitation. In Experiment 3, the same 16 gratings appeared as one large superset, and therefore the task only required one summary representation for size and another one for orientation. Equal simultaneous-sequential performance indicated that between-feature summaries are capacity free. These findings challenge the view that within-feature summaries drive a global sense of visual continuity across areas of the peripheral visual field, and suggest a shift in focus to seeking an understanding of how between-feature summaries in one area of the environment control behavior.

In the framework of Reverse Hierarchy Theory it was suggested that initial vision at a glance brings the gist of the scene to conscious perception using explicit high cortical level representations, which are initially built by implicit bottom-up processing (Hochstein & Ahissar, 2002). Only later return to lower cortical level representations introduces local details to conscious perception. Global statistics of similar elements are perceived rapidly and accurately, suggesting they are included in the initial perception of the gist of the scene, not depending on prior conscious perception of local details. Patients with unilateral spatial neglect have difficulty responding to elements in their contralesional hemifield. However, this deficit is especially pronounced for tasks that require focused attention, i.e., are dependent on the reverse-hierarchy return. We review recent studies that indicate that perception of global statistics is among the spread attention tasks that are somewhat spared from this deficit. Combining these results, we suggest that perhaps the function of global statistics perception might include serving as a basic percept required for finding salient deviants from the mean, as in rapid odd element feature search paradigms, and perhaps subsequently focusing attention to them.

Various studies have identified systematic errors, such as spatial compression, when observers report the locations of objects displayed around the time of saccades. Localization errors also occur when holding spatial representations in visual working memory. Such errors, however, have not been examined in the context of eye blinks. In this study, we examined the effects of blinks and saccades when observers reproduced the locations of a set of briefly presented, randomly placed discs. Performance was compared with a fixation-only condition in which observers simply held these representations in working memory for the same duration; this allowed us to elucidate the relationship between the perceptual phenomena related to blinks, saccades, and visual working memory. Our results indicate that the same amount of spatial compression is experienced prior to a blink as is experienced in the control fixation-only condition, suggesting that blinks do not increase compression above that occurring from holding a spatial representation in visual memory. Saccades, however, tend to increase these compression effects and produce translational shifts both toward and away from saccade targets (depending on the time of the saccade onset in relation to the stimulus offset). A higher numerosity recall capacity was also observed when stimuli were presented prior to a blink in comparison with the other conditions. These findings reflect key differences underlying blinks and saccades in terms of spatial compression and translational shifts. Such results suggest that separate mechanisms maintain perceptual stability across these visual events.