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Classic change blindness is the phenomenon where seemingly obvious changes that coincide with visual disruptions (such as blinks or brief blanks) go unnoticed by an attentive observer. Some early work into the causes of classic change blindness suggested that any pre-change stimulus representation is overwritten by a representation of the altered post-change stimulus, preventing change detection. However, recent work revealed that, even when observers do maintain memory representations of both the pre- and post-change stimulus states, they can still miss the change, suggesting that change blindness can also arise from a failure to compare the stored representations. Here, we studied slow change blindness, a related phenomenon that occurs even in the absence of visual disruptions when the change occurs sufficiently slowly, to determine whether it could be explained by conclusions from classic change blindness. Across three different slow change blindness experiments we found that observers who consistently failed to notice the change had access to at least two memory representations of the changing display. One representation was precise but short lived: a detailed representation of the more recent stimulus states, but fragile. The other representation lasted longer but was fairly general: stable but too coarse to differentiate the various stages of the change. These findings suggest that, although multiple representations are formed, the failure to compare hypotheses might not explain slow change blindness; even if a comparison were made, the representations would be too sparse (longer term stores) or too fragile (short-lived stores) for such comparison to inform about the change.

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Change blindness is the phenomenon that occurs when an observer fails to notice what would seem to be obvious changes in the features of a visual stimulus. Researchers can induce this experimentally by including visual disruptions (such as brief blanks) that coincide with the changes in question. However, change blindness can also occur in the absence of these disruptions if a change occurs sufficiently slowly. This "slow" or "gradual" change blindness phenomenon has not been extensively researched. Two plausible practical reasons for this are that there are few slow-change stimuli available, and that it is difficult to collect trial-specific responses without affecting expectations on later trials. Here, we describe a novel, semi-automatic procedure for quickly generating many slow-change stimuli. This procedure creates stimuli that have been specifically designed to allow assessment of change blindness on individual trials without influencing subsequent trials. We include the results of three validation experiments that demonstrate that these stimuli are effective and suitable for use in systematic studies of slow change blindness.

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An altered use of context and experience to interpret incoming information has been posited to explain schizophrenia symptoms. The visual system can serve as a model system for examining how context and experience guide perception and the neural mechanisms underlying putative alterations. The influence of prior experience on current perception is evident in visual aftereffects, the perception of the "opposite" of a previously viewed stimulus. Aftereffects are associated with neural adaptation and concomitant change in strength of lateral inhibitory connections in visually responsive neurons. In a previous study, we observed stronger aftereffects related to orientation (tilt aftereffects) but not luminance (negative afterimages) in individuals diagnosed with schizophrenia, which we interpreted as potentially suggesting altered cortical (but not subcortical) adaptability and local changes in excitatory-inhibitory interactions. Here, we tested whether stronger tilt aftereffects were specific to individuals with schizophrenia or extended to individuals with bipolar disorder. We measured tilt aftereffects and negative afterimages in 32 individuals with bipolar disorder, and compared aftereffect strength to a previously reported group of 36 individuals with schizophrenia and 22 healthy controls. We observed stronger tilt aftereffects, but not negative afterimages, in individuals with schizophrenia as compared to both controls and individuals with bipolar disorder, who did not differ from each other. These results mitigate concerns that stronger tilt aftereffects in schizophrenia are a consequence of medication or of the psychosocial consequences of a severe mental illness.

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The self-generation effect refers to the finding that people's memory for information tends to be better when they generate it themselves. Counterintuitively, when proofreading, this effect may make it more difficult to detect mistakes in one's own writing than in others' writing. We investigated the self-generation effect and sources of individual differences in proofreading performance in two eye-tracking experiments. Experiment 1 failed to reveal a self-generation effect. Experiment 2 used a studying manipulation to induce overfamiliarity for self-generated text, revealing a weak but non-significant self-generation effect. Overall, word errors (i.e., wrong words) were detected less often than non-word errors (i.e., misspellings), and function word errors were detected less often than content word errors. Fluid intelligence predicted proofreading performance, whereas reading comprehension, working memory capacity, processing speed, and indicators of miserly cognitive processing did not. Students who made more text fixations and spent more time proofreading detected more errors.

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When faced with ambiguous visual input, observers may experience various perceptual interpretations of the same input. Indeed, such input can cause perception to unpredictably switch between interpretations over time. Theories of such so-called multistable perception broadly fall into two categories: top-down theories that emphasize dependence on higher-level cognitive factors such as knowledge, and bottom-up theories that suggest more vital involvement of aspects of lower-order information processing such as adaptation in the visual system. Most present-day accounts hold that both factors play a role, so that perceptual reversals arise inevitably due to factors like adaptation, yet can be delayed or hastened by higher-level cognitive influences. We revisited a body of work that shows the occurrence of perceptual reversals to depend dramatically on the observer's knowledge that the input is, indeed, ambiguous: without such knowledge many observers in that work did not experience any reversals, in apparent conflict with the idea that reversals are inevitable. We used an ambiguous animation that allowed subjects to report perceptual reversals without realizing the ambiguity. We found that subjects who were aware of the animation's ambiguity reported slightly more perceptual reversals than uninformed subjects, but that this between-group difference was small, and was overshadowed by inter-observer variability within each group. These findings suggest that knowledge of ambiguity can influence perception of ambiguous stimuli, but only mildly, in keeping with most present-day accounts. We discuss potential explanations for the discrepancy with the earlier work.

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Two largely separate lines of research have documented altered pupillary dynamics in individuals diagnosed with schizophrenia. An older set of studies has demonstrated reductions in the pupillary light reflex (PLR) in individuals with schizophrenia; however, clinical and cognitive correlates of this blunted PLR have been relatively unexplored. More recently, a large body of work has demonstrated reductions in pupillary dilation in response to cognitive demands in individuals with schizophrenia, and the degree of this blunted pupil dilation has been related to more severe cognitive deficits and motivational negative symptoms. These clinically relevant alterations in the cognitive modulation of pupil size have been interpreted as reflecting insufficient information processing resources or inappropriate effort allocation. To begin to bridge these two lines of work, we investigated the PLR in 34 individuals with schizophrenia and 30 healthy controls and related the amplitude of the PLR to motivational negative symptoms and cognitive performance. Consistent with prior work, we found that the PLR was reduced in individuals with schizophrenia, and furthermore, that these measurements were highly reliable across individuals. Blunted constriction was associated with more severe motivational negative symptoms and poorer working memory among individuals with schizophrenia. These observed correlates provide a bridge between older literature documenting an altered PLR and more recent work reporting associations between negative symptoms, cognition, and blunted pupillary dilation in response to cognitive demands in individuals with schizophrenia. We provide possible mechanistic interpretations of our data and consider a parsimonious explanation for reduced cognitive- and light-related modulation of pupil size.

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Some images evoke bistable percepts: two different visual experiences seen in alternation while continuously viewing an unchanged stimulus. The Necker Cube and Rubin's Vase are classic examples, each of which gives alternating percepts of different shapes. Other bistable percepts are alternating colors or directions of motion. Although stimuli that result in salient bistability are rare and sometimes cleverly constructed to emphasize ambiguity, they have been influential for over 150 years, since the work of von Helmholtz, who considered them to be evidence for perceptual visual processes that interpret retinal stimuli. While bistability in natural viewing is uncommon, the main point of this review is that implicit ambiguity in visual neural representations is pervasive. Resolving ambiguity, therefore, is a fundamental and ubiquitous process of vision that routinely affects what we see, not an oddity arising from cleverly crafted images. This review focuses on the causes of widespread ambiguity, historical perspectives on it, and modern knowledge and theory about resolving it.

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The pupil provides a rich, non-invasive measure of the neural bases of perception and cognition and has been of particular value in uncovering the role of arousal-linked neuromodulation, which alters both cortical processing and pupil size. But pupil size is subject to a multitude of influences, which complicates unique interpretation. We measured pupils of observers experiencing perceptual multistability-an ever-changing subjective percept in the face of unchanging but inconclusive sensory input. In separate conditions, the endogenously generated perceptual changes were either task-relevant or not, allowing a separation between perception-related and task-related pupil signals. Perceptual changes were marked by a complex pupil response that could be decomposed into two components: a dilation tied to task execution and plausibly indicative of an arousal-linked noradrenaline surge, and an overlapping constriction tied to the perceptual transient and plausibly a marker of altered visual cortical representation. Constriction, but not dilation, amplitude systematically depended on the time interval between perceptual changes, possibly providing an overt index of neural adaptation. These results show that the pupil provides a simultaneous reading on interacting but dissociable neural processes during perceptual multistability, and suggest that arousal-linked neuromodulator release shapes action but not perception in these circumstances.

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There are clear benefits to using an online environment for human subjects' research, for instance, rapid data collection and access to a diverse body of potential participants. One distinct drawback of online environments as compared to laboratory environments is the relative lack of control over experiment conditions. For research into human vision, a specific concern is the relative lack of control over angular stimulus dimension in an online setting. This paper examines three approaches to estimating a participant's viewing distance online, and quantifies the magnitude of the error in angular stimulus size associated with each method. For each method, the average expected error is smaller than 20% of the intended stimulus size, and for the best method it is close to 10%. This paper provides a discussion of the benefits and drawbacks of each of the three methods, as well as parameter values and computer code that will facilitate the use of these methods in future online studies.

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When observers view a perceptually bistable stimulus, their perception changes stochastically. Various studies have shown across-observer correlations in the percept durations for different bistable stimuli including binocular rivalry stimuli and bistable moving plaids. Previous work on binocular rivalry posits that neural inhibition in the visual hierarchy is a factor involved in the perceptual fluctuations in that paradigm. Here, in order to investigate whether between-observer variability in cortical inhibition underlies correlated percept durations between binocular rivalry and bistable moving plaid perception, we used center-surround suppression as a behavioral measure of cortical inhibition. We recruited 217 participants in a test battery that included bistable perception paradigms as well as a center-surround suppression paradigm. While we were able to successfully replicate the correlations between binocular rivalry and bistable moving plaid perception, we did not find a correlation between center-surround suppression strength and percept durations for any form of bistable perception. Moreover, the results from a mediation analysis indicate that center-surround suppression is not the mediating factor in the correlation between binocular rivalry and bistable moving plaids. These results do not support the idea that cortical inhibition can explain the between-observer correlation in mean percept duration between binocular rivalry and bistable moving plaid perception.

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Aerobic fitness is consistently and robustly associated with superior performance on assessments of cognitive control. One potential mechanism underlying this phenomenon is activation of the locus-coeruleus. Specifically, individuals with greater aerobic fitness may be better able to sustain engagement in a cognitively demanding task via a superior ability to meet the metabolic demands of this neural system. Accordingly, the present investigation examined 1) the relationship between aerobic fitness and phasic activation of the locus-coeruleus (indexed using pupillometry) and 2) the potential mediating influence of locus-coeruleus activity on the relationship between aerobic fitness and cognitive task performance. Participants performed an inhibition task while their pupillary responses were measured using an infrared eye tracker. A VO2max test was then performed to determine individuals' aerobic fitness levels. Consistent with previous research, higher levels of aerobic fitness were related to shorter reaction time. However, phasic activity of the locus-coeruleus did not mediate this relationship - nor did it relate to aerobic fitness level. These results suggest that aerobic fitness does not relate to differences in locus-coeruleus activity in the context of cognitive control in college-aged adults.

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Individuals with schizophrenia may fail to appropriately use temporal context and apply past environmental regularities to the interpretation of incoming sensory information. Here we use the visual system as a test bed for investigating how prior experience shapes perception in individuals with schizophrenia. Specifically, we use visual aftereffects, illusory percepts resulting from prior exposure to visual input, to measure the influence of prior events on current processing. At a neural level, visual aftereffects arise due to attenuation in the responses of neurons that code the features of the prior stimulus (neuronal adaptation) and subsequent disinhibition of neurons signaling activity at the opposite end of the feature dimension. In the current study, we measured tilt aftereffects and negative afterimages, 2 types of aftereffects that reflect, respectively, adaptation of cortical orientation-coding neurons and adaptation of subcortical and retinal luminance-coding cells in persons with schizophrenia (PSZ; n = 36) and demographically matched healthy controls (HC; n = 22). We observed stronger tilt aftereffects in PSZ compared to HC, but no difference in negative afterimages. Stronger tilt aftereffects were related to more severe negative symptoms. These data suggest oversensitivity to recent regularities, in the form of stronger visual adaptation, at cortical, but not subcortical, levels in schizophrenia. (PsycInfo Database Record (c) 2021 APA, all rights reserved).

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Binocular rivalry suppression is thought to necessarily require local interocular conflict: the presence of incompatible image elements, such as orthogonal contours, in retinally corresponding regions of two monocular displays. Whether suppression can also be driven by conflict at the level of spatially nonlocal surface or object representations is unclear. Here, we kept local contour conflict constant while varying global conflict, defined by the gestalt formed by the two monocular displays. Specifically, each eye was presented with a grid of image elements (crosses or plusses), placed such that the two eyes' individual grid elements did not directly overlap but the grids as a whole did. In a "shared motion" condition, all elements moved in unison, inviting a gestalt made up of all elements across both eyes; in a "different motions" condition, the elements' trajectories differed between eyes, inviting a gestalt of two overlapping surfaces, each associated with one eye. Perceptual disappearances of image elements occurred more readily in the different motions condition, an observation that could not be explained by any between-condition differences in local contour conflict. In a second experiment, we furthermore established that, whereas perceptual disappearances in the shared motion condition tended to involve a single element at a time, in the different motions condition, multiple elements belonging to the same gestalt often disappeared together. These findings indicate that, even though binocular rivalry may critically rely on inhibition due to locally incompatible image elements, this inhibition also depends on the global gestalt to which these elements contribute.

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Research in radiology and visual cognition suggest that finding one target during visual search may result in increased misses for a second target, an effect known as subsequent search misses (SSM). Here, we demonstrate that the common method of calculating second-target detection performance is biased and could produce spurious SSM effects. We describe the source of that bias and document factors that influence its magnitude. We use a modification of signal-detection theory to develop a novel, unbiased method of calculating the expected value for dual-target performance under the null hypothesis. We then apply our novel method to two of our data sets that showed modest SSM effects when calculated in the traditional manner. Our correction reduced the effect size to the point that there was no longer a significant SSM effect. We then applied our method to a published data set that had a larger effect size when calculated using the traditional calculation as well as when using an alternative calculation that was recently proposed to account for biases in the traditional method. We find that both the traditional method and the recently proposed alternative substantially overestimate the magnitude of the SSM effect in these data, but a significant SSM effect persisted even with our calculation. We recommend that future SSM studies use our method to ensure accurate effect-size estimates, and suggest that the method be applied to reanalyze published results, particularly those with small effect sizes, to rule out the possibility that they were spurious.

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Priming of attention shifts involves the reduction in search RTs that occurs when target location or target features repeat. We used functional magnetic resonance imaging to investigate the neural basis of such attentional priming, specifically focusing on its temporal characteristics over trial sequences. We first replicated earlier findings by showing that repetition of target color and of target location from the immediately preceding trial both result in reduced blood oxygen level-dependent (BOLD) signals in a cortical network that encompasses occipital, parietal, and frontal cortices: lag-1 repetition suppression. While such lag-1 suppression can have a number of explanations, behaviorally, the influence of attentional priming extends further, with the influence of past search trials gradually decaying across multiple subsequent trials. Our results reveal that the same regions within the frontoparietal network that show lag-1 suppression, also show longer term BOLD reductions that diminish over the course of several trial presentations, keeping pace with the decaying behavioral influence of past target properties across trials. This distinct parallel between the across-trial patterns of cortical BOLD and search RT reductions, provides strong evidence that these cortical areas play a key role in attentional priming.

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Although binocular rivalry is different from other perceptually bistable phenomena in requiring interocular conflict, it also shares numerous features with those phenomena. This raises the question of whether, and to what extent, the neural bases of binocular rivalry and other bistable phenomena overlap. Here we examine this question using an individual-differences approach. In a first experiment, observers reported perception during four binocular rivalry tasks that differed in the features and retinal locations of the stimuli used. Perceptual dominance durations were highly correlated when compared between stimuli that differed in location only. Correlations were substantially weaker, however, when comparing stimuli comprised of different features. Thus, individual differences in binocular-rivalry perception partly reflect a feature-specific factor that is not shared among all variants of binocular rivalry. Our second experiment again included several binocular rivalry variants, but also a different form of bistability: moving plaid rivalry. Correlations in dominance durations between binocular rivalry variants that differed in feature content were again modest. Moreover, and surprisingly, correlations between binocular rivalry and moving plaid rivalry were of similar magnitude. This indicates a second, more general, factor underlying individual differences in binocular rivalry perception: one that is shared across binocular rivalry and moving plaid rivalry. We propose that the first, feature-specific factor corresponds to feature-tuned mechanisms involved in the treatment of interocular conflict, whereas the second, general factor corresponds to mechanisms involved in representing surfaces. These latter mechanisms would operate at a binocular level and be central to both binocular rivalry and other forms of bistability.

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When the two eyes' processing streams meet in visual cortex, two things can happen: sufficiently similar monocular inputs are combined into a fused representation, whereas markedly different inputs engage in rivalry. Interestingly, the emergence of rivalry appears to require attention. Withdrawing attention causes the alternating monocular dominance that characterizes rivalry to cease, apparently allowing both monocular signals to be processed simultaneously. What happens to these signals in this case, however, remains something of a mystery; are they fused into an integrated representation? In a set of experiments, we show this not to be the case: visual aftereffects are consistent with the simultaneous yet separate presence of two segregated monocular representations, rather than a joint representation. These results provide evidence that dichoptic vision without attention prompts a third and previously unknown mode, where both eyes' inputs receive equal processing, but escape interocular fusion.

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Psychosis-a cardinal symptom of schizophrenia-has been associated with a failure to appropriately create or use stored regularities about past states of the world to guide the interpretation of incoming information, which leads to abnormal perceptions and beliefs. The visual system provides a test bed for investigating the role of prior experience and prediction, as accumulated knowledge of the world informs our current perception. More specifically, the strength of visual aftereffects, illusory percepts that arise after prolonged viewing of a visual stimulus, can serve as a valuable measure of the influence of prior experience on current visual processing. In this paper, we review findings from a largely older body of work on visual aftereffects in schizophrenia, attempt to reconcile discrepant findings, highlight the role of antipsychotic medication, consider mechanistic interpretations for behavioral effects, and propose directions for future research.

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Single bouts of exercise have been observed to enhance numerous domains of cognition including inhibitory aspects of cognitive control and neuroelectric indices of attention. Given that the locus-coeruleus norepinephrine system regulates alertness and attention, this system may underlie these exercise-induced enhancements. The present study used pupillometry to examine the extent to which a single bout of exercise induces changes in aspects of locus-coeruleus activation, as well as the extent to which changes in locus-coeruleus activation were associated with changes in inhibition and neuroelectric indices of attention. Using a within-participants crossover design, behavioral, neuroelectric, and pupillometric measures were assessed in response to an inhibitory control task before and after 20-min of either aerobic exercise or an active-control condition during two separate, counterbalanced sessions. The aerobic exercise condition consisted of walking/jogging on a motor driven treadmill at an intensity of approximately 70% of age-predicted maximum heart rate. The active control condition consisted of walking on the treadmill at 0.5 mph and 0% grade. Replicating prior findings, enhancements in both reaction time and neuroelectric indices of attention were observed in response to the exercise condition. However, neither the exercise nor the active control conditions were observed to induce changes in activation of the locus-coeruleus as indexed by pupil size, and changes in activation of the locus-coeruleus were not associated with exercise-induced changes in inhibition and neuroelectric indices of attention. Accordingly, these findings provide evidence to suggest that activation of the locus-coeruleus is not a mechanism underlying exercise-induced enhancements in cognition.

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In primates, the two eyes offer substantially overlapping views of the world. The information they provide is merged into a single, integrated, representation in visual cortex. New evidence changes long-standing ideas about how and where in the processing stream this happens.

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