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It is widely assumed that subliminal word priming is case insensitive and that a short SOA (

Although visual search studies have primarily focused on search behavior, concealment behavior is also important in the real world. However, previous studies in this regard are limited in that their findings about search and concealment strategies are restricted to the spatial (two-dimensional) domain. Thus, this study evaluated strategies during three-dimensional and temporal (i.e., spatiotemporal) search and concealment to determine whether participants would indicate where they would hide or find a target in a temporal sequence of items. The items were stacked in an upward (Experiments 1-3) or downward (Experiment 4) direction and three factors were manipulated: scenario (hide vs. seek), partner type (friend vs. foe), and oddball (unique item in the sequence; present vs. absent). Participants in both the hide and seek scenarios frequently selected the oddball for friends but not foes, which suggests that they applied common strategies because the oddball automatically attracts attention and can be readily discovered by friends. Additionally, a principle unique to the spatiotemporal domain was revealed, i.e., when the oddball was absent, participants in both scenarios frequently selected the topmost item of the stacked layer for friends, regardless of temporal order, whereas they selected the first item in the sequence for foes, regardless of the stacked direction. These principles were not affected by visual masking or number of items in the sequence. Taken together, these results suggest that finding and hiding positions in the spatiotemporal domain rely on the presence of salient items and physical accessibility or temporal remoteness, according to partner type.

In a novel integration of research designs, we tested for unconscious perception effects at an unattended stimulus location using a focused attention paradigm (Lachter, J., Forster, K. I., & Ruthru...

Ensemble perception-the encoding of objects by their group properties-is known to be resistant to outlier noise. However, this resistance is somewhat paradoxical: how can the visual system determine which stimuli are outliers without already having derived statistical properties of the ensemble? A simple solution would be that ensemble perception is not a simple, one-step process; instead, outliers are detected through iterative computations that identify items with high deviance from the mean and reduce their weight in the representation over time. Here we tested this hypothesis. In Experiment 1, we found evidence that outliers are discounted from mean orientation judgments, extending previous results from ensemble face perception. In Experiment 2, we tested the timing of outlier rejection by having participants perform speeded judgments of sets with or without outliers. We observed significant increases in reaction time (RT) when outliers were present, but a decrease compared to no-outlier sets of matched range suggesting that range alone did not drive RTs. In Experiment 3 we tested the timing by which outlier noise reduces over time. We presented sets for variable exposure durations and found that noise decreases linearly over time. Altogether these results suggest that ensemble representations are optimized through iterative computations aimed at reducing noise. The finding that ensemble perception is an iterative process provides a useful framework for understanding contextual effects on ensemble perception. (PsycInfo Database Record (c) 2020 APA, all rights reserved).

International audience; Interpersonal distance, an essential component of social interaction, is modulated by the emotion conveyed by others and associated physiological response. However, in modern societies with overcrowded and hyperstimulating environments, we can only surreptitiously glimpse the faces of others in order to quickly make behavioral adjustments. How this impacts social interactions is not yet well understood. In the present study, we investigated this issue by testing whether facial expressions that are difficult to identify modify the physiological response (Electrodermal Activity, EDA) and subsequent judgment of interpersonal comfort distance. We recorded participants’ EDA while they provided comfort judgments to interpersonal distances with a Point-Light Walker (PLW). The PLW, with an emotionally neutral gait, moved toward and crossed participants at various distances after the latter were exposed to a negative (anger), positive (happiness) or neutral facial expression presented at the perceptual threshold. Bayesian analyses of the data revealed an increase versus decrease of interpersonal comfort distance with the PLW depending on the negative versus positive emotional valence of the facial expression. They also showed an increase in EDA when the approaching PLW violated interpersonal comfort distance after participants were exposed to an angry facial expression. These effects correlated with the subjective assessment of the arousal of facial expressions. Thus, previous exposure to barely visible facial expressions can alter the representation of social comfort space and the physiological response associated with a violation of interpersonal comfort distances, depending on the valence and arousal of the emotional social stimuli.

We investigated if the subliminal processing of threatening animal (snakes and spiders) and neutral object (cars and houses) stimuli can influence the discrimination of a subsequent visible stimulus. The prime and target pair were either identical, of the same category but with different physical features, or different in category and physical features. In two experiments, participants discriminated the basic level category (e.g. snake vs. spider) of a visible target stimulus that had been preceded by a visible or perceptually invisible prime stimulus. One experiment used visual masking to render prime stimuli perceptually invisible and the other used continuous flash suppression (CFS). Priming effects were demonstrated in both experiments when the prime was visible but not when the prime was rendered perceptually invisible. These findings demonstrate that conscious awareness could be required in the perceptual discrimination of threatening animal and neutral object images at their specific basic level category.

Charting mental acts that succeed or fail under unconscious instances of cognition informs debates on the nature and potential functions of consciousness. A prominent method to exclude conscious contributions to cognition is to render visual stimuli unconscious by short and pattern-masked presentations. Here, we explore a combination of visual masking and pixel noise added to visual stimuli as a method to adapt discriminability in a fine-grained fashion to subject- and stimulus-specific estimates of perceptual thresholds. Estimates of the amount of pixel noise corresponding to perceptual thresholds are achieved by psychometric adaptive algorithms in an identification task. Afterwards, the feasibility of instrumental conditioning is tested at four levels of cue discriminability relative to previously acquired estimates of perceptual thresholds. In contrast to previous reports (Pessiglione et al., 2008), no evidence for the feasibility of instrumental condition was gathered when contributions of conscious cognition were excluded.

In this study we examined whether grouping by luminance similarity and grouping by connectedness can occur in the absence of visual awareness, using a priming paradigm and two methods to render the prime invisible, CFS and sandwich masking under matched conditions. For both groupings, significant response priming effects were observed when the prime was reported invisible under sandwich masking, but none were obtained under CFS. These results provide evidence for unconscious grouping, converging with previous findings showing that visual awareness is not essential for certain perceptual organization processes to occur. They are also consistent with findings indicating that processing during CFS is limited, and suggest the involvement of higher visual areas in perceptual organization. Moreover, these results demonstrate that whether a process can occur without awareness is dependent on the level at which the suppression induced by the method used for rendering the stimulus inaccessible to awareness takes place.

Continuous flash suppression (CFS) involves the presentation of a rapidly changing Mondrian sequence to one eye and a static target in the other eye. Targets presented in this manner remain suppressed for several seconds at a time, and this has seen the prevalent use of CFS in studies of unconscious visual processes. However, the mechanisms behind CFS remain unclear, complicating its use and the comprehension of results obtained with the paradigm. For example, some studies report observations indicative of faster, visual masking processes whereas others suggest slower, rivalry processes. To reconcile this discrepancy, this study investigates the effect of temporal frequency content and Mondrian pattern structure on CFS suppression. Our results show predominant influences of spatial edges and low temporal-frequency content, which are similar to binocular rivalry, affording a parsimonious alternative in unifying the two paradigms.

To keep track of dynamically changing objects in one’s environment, it is necessary to individuate them from other objects, both temporally and spatially. Spatially, objects can be selected from nearby distractors using selective attention. Temporally, object updating processes incorporate new information into existing representations over time. Both of these processes have been implicated in a type of visual masking called object-substitution masking (OSM). Previous studies have found that the number of distractors (impacting selective attention) interacts with the strength of OSM. However, it has been suggested that this interaction is an artifact of ceiling performance at low set sizes, rather than necessitating a failure of attention during masking. Using event-related potentials (ERPs), we examined whether set size and masking interact as measured by markers of selective attention (N2pc) and visual working memory consolidation/maintenance (SPCN). Set size was found to affect the N2pc (200–350 ms) and late SPCN (500–650 ms), reflecting increased demands on selective attention and unnecessary storage respectively. An early window of the SPCN (350–500 ms) was affected by masking, suggesting that OSM influences object consolidation processes in this window, independent of the number of distractors. Overall, it was found that selective attention and visual awareness are dissociable neural processes in OSM, and that they are independently affected by set size and masking manipulations. Moreover, we found that the early SPCN may reflect disruptions to object consolidation, potentially revealing a neural mechanism supporting an object individuation-through-updating account of OSM.

Perceptual conscious experiences result from non-conscious processes that precede them. We document a new characteristic of the cognitive system: the speed with which visual meaningful stimuli are prioritized to consciousness over competing noise in visual masking paradigms. In ten experiments (N = 399) we find that an individual's non-conscious visual prioritization speed (NVPS) is ubiquitous across a wide variety of stimuli, and generalizes across visual masks, suppression tasks, and time. We also find that variation in NVPS is unique, in that it cannot be explained by variation in general speed, perceptual decision thresholds, short-term visual memory, or three networks of attention (alerting, orienting and executive). Finally, we find that NVPS is correlated with subjective measures of sensitivity, as they are measured by the Highly Sensitive Person scale. We conclude by discussing the implications of variance in NVPS for understanding individual variance in behavior and the neural substrates of consciousness.

Blindsight patients with damage to the visual cortex can discriminate objects but report no conscious visual experience. This provides an intriguing opportunity to allow the study of subjective awareness in isolation from objective performance capacity. However, blindsight is rare, so one promising way to induce the effect in neurologically intact observers is to apply transcranial magnetic stimulation (TMS) to the visual cortex. Here, we used a recently-developed criterion-free method to conclusively rule out an important alternative interpretation of TMS-induced performance without awareness: that TMS-induced blindsight may be just due to conservative reporting biases for conscious perception. Critically, using this criterion-free paradigm we have previously shown that introspective judgments were optimal even under visual masking. However, here under TMS, observers were suboptimal, as if they were metacognitively blind to the visual disturbances caused by TMS. We argue that metacognitive judgments depend on observers’ internal statistical models of their own perceptual systems, and introspective suboptimality arises when external perturbations abruptly make those models invalid -- a phenomenon that may also be happening in actual blindsight.

It has been suggested that unconscious semantic processing is stimulus-dependent, and that pictures might have privileged access to semantic content. Those findings led to the hypothesis that unconscious semantic priming effect for pictorial stimuli would be stronger as compared to verbal stimuli. This effect was tested on pictures and words by manipulating the semantic similarity between the prime and target stimuli. Participants performed a masked priming categorization task for either words or pictures with three semantic similarity conditions: strongly similar, weakly similar, and non-similar. Significant differences in reaction times were only found between strongly similar and non-similar and between weakly similar and non-similar, for both pictures and words, with faster overall responses for pictures as compared to words. Nevertheless, pictures showed no superior priming effect over words. This could suggest the hypothesis that even though semantic processing is faster for pictures, this does not imply a stronger unconscious priming effect.

Object individuation: is the process whereby the brain infers that dynamic input reflects multiple discrete objects, rather than a single, continuing object over time. Object substitution masking: is a popular method for operationalizing object individuation inferences in the laboratory. Although object substitution masking was historically thought to interact with attentional processes, an emerging body of literature indicates that this form of visual masking is impervious to some attentional manipulations. However, one form of attention that has not been systematically studied in relation to object-substitution masking is endogenous attentional orienting. This is important because in other domains, endogenous attentional orienting has been found to have qualitatively distinct effects from other forms of attention, including impacting visual perception when other forms of attention do not. Therefore, if attention does interact with object individuation processes, then endogenous attentional orienting is the most likely candidate mechanism for such a relationship. Here, therefore, the impact of endogenous attentional on object-substitution masking was tested. Across 2 experiments, although endogenous attentional orienting impacted overall target perception, it had no impact on object substitution masking. This implies that object individuation inferences are indeed independent of attention. (PsycINFO Database Record (c) 2019 APA, all rights reserved).

A visual stimulus is perceived as shorter when a short sound is presented immediately before and after the visual target than when the visual target appears alone. It remains unclear whether the time compression occurs in an intramodal condition. Therefore, the present study examined how and when non-target sandwiching stimuli affect the perceived filled duration of target visual stimuli. We further hypothesized that this effect could be modulated by temporal and spatial proximity between the target and non-target stimuli. Experiments 1a, 1b, and 2 showed that non-target stimuli could decrease the perceived duration only when the inter-stimulus interval between these stimuli was 0 ms, using time reproduction and category estimation methods. Experiments 3 revealed that the time compression effect did not occur when both the non-target preceding and trailing stimuli were spatially distinct from the target. Experiment 4 demonstrated that either the preceding or trailing stimulus induced the time compression effect when the non-target stimuli were presented at the same position as the target stimuli. We discuss the implications of the time compression effect induced by non-target sandwiching stimuli with reference to the Scalar Expectancy Theory and the Neural Readout Model. We speculated that the attenuation of neural responses to the target via visual masking or perceptual grouping may be attributable to the time compression effect.

The level of processing (LoP) hypothesis proposes that low-level stimulus perception (i.e., stimulus energy and features) is a graded process whereas high-level (i.e., letters, words, meaning) stimulus perception is all-or-none. In the present study, we set up a visual masking design in order to examine the nature of visual awareness at stimulus energy (i.e., detection task) and feature levels (identification task) at specific individual target durations (13, 27, 40, 53, and 80 ms). We manipulated the strength of the masking to produce different visibility conditions and gathered participants' subjective (across a 4-point awareness scale) and objective (accuracy levels) awareness performances. We found that intermediate ratings (i.e., ratings 2 and 3, which index graded awareness experiences) were used in more than 50% of the trials for target presentations of 27, 40, 53, and 80 ms. In addition, objective accuracy performances for target presentations of 27 and 80 ms produced linearly increasing detection and identification accuracies across the awareness scale categories, respectively. Overall, our results suggest that visual awareness at energy and feature levels of stimulus perception may be graded. Furthermore, we found a divergence in detection and identification performance results, which emphasizes the need for an adequate election of target durations when studying different perceptual processes such as detection versus more complex stimulus identification processes. Finally, "clarity" in the perceptual awareness scale should be exhaustively defined depending on the level of processing of the stimulus, as participants may recalibrate the meaning of the different awareness categories depending on task demands.

The mere presence of information in the brain does not always mean that this information is available to consciousness (de-Wit, Alexander, Ekroll, & Wagemans, 2016). Experiments using paradigms such as binocular rivalry, visual masking, and the attentional blink have shown that visual information can be processed and represented by the visual system without reaching consciousness. Using multivariate pattern analysis (MVPA) and magneto-encephalography (MEG), we investigated the temporal dynamics of information processing for unconscious and conscious stimuli. We decoded stimulus information from the brain recordings while manipulating visual consciousness by presenting stimuli at threshold contrast in a backward masking paradigm. Participants’ consciousness was measured using both a forced-choice categorisation task and self-report. We show that brain activity during both conscious and non-conscious trials contained stimulus information, and that this information was enhanced in conscious trials. Overall, our results indicate that visual consciousness is characterised by enhanced neural activity representing the visual stimulus, and that this effect arises as early as 180 ms post-stimulus onset.

Recent studies argued that unconscious visual information could access the working memory, however, it is still unclear whether the central executive could be activated unconsciously. We investigated, using a delayed match-to-sample task, whether the central executive is an unconscious process. In the experiment of the present study, participants were asked to compare the locations of two given visual targets. Both targets (or one of the two targets, depending on the experimental condition) were masked by a visual masking paradigm. The results showed an above-chance-level performance even in the condition that participants compared two unconscious targets. However, when the trials with the non-visual conscious experience of the target were removed from the analysis, the performance was no longer significantly different from chance level. Our results suggest that the central executive could be activated unconsciously by some level of stimulus signal, that is still below the threshold for a subjective report.

We used the attentional blink (AB) paradigm to investigate the processing stage at which extraction of summary statistics from visual stimuli ("ensemble coding") occurs. Experiment 1 examined whether ensemble coding requires attentional engagement with the items in the ensemble. Participants performed two sequential tasks on each trial: gender discrimination of a single face (T1) and estimating the average emotional expression of an ensemble of four faces (or of a single face, as a control condition) as T2. Ensemble coding was affected by the AB when the tasks were separated by a short temporal lag. In Experiment 2, the order of the tasks was reversed to test whether ensemble coding requires more working-memory resources, and therefore induces a larger AB, than estimating the expression of a single face. Each condition produced a similar magnitude AB in the subsequent gender-discrimination T2 task. Experiment 3 additionally investigated whether the previous results were due to participants adopting a subsampling strategy during the ensemble-coding task. Contrary to this explanation, we found different patterns of performance in the ensemble-coding condition and a condition in which participants were instructed to focus on only a single face within an ensemble. Taken together, these findings suggest that ensemble coding emerges automatically as a result of the deployment of attentional resources across the ensemble of stimuli, prior to information being consolidated in working memory.

Visual masking and attention have been known to control the transfer of information from sensory memory to visual short-term memory. A natural question is whether these processes operate independently or interact. Recent evidence suggests that studies that reported interactions between masking and attention suffered from ceiling and/or floor effects. The objective of the present study was to investigate whether metacontrast masking and attention interact by using an experimental design in which saturation effects are avoided. We asked observers to report the orientation of a target bar randomly selected from a display containing either two or six bars. The mask was a ring that surrounded the target bar. Attentional load was controlled by set-size and masking strength by the stimulus onset asynchrony between the target bar and the mask ring. We investigated interactions between masking and attention by analyzing two different aspects of performance: (i) the mean absolute response errors and (ii) the distribution of signed response errors. Our results show that attention affects observers' performance without interacting with masking. Statistical modeling of response errors suggests that attention and metacontrast masking exert their effects by independently modulating the probability of "guessing" behavior. Implications of our findings for models of attention are discussed.

The visual system is constantly bombarded with dynamic input. In this context, the creation of enduring object representations presents a particular challenge. We used object-substitution masking (OSM) as a tool to probe these processes. In particular, we examined the effect of target-like stimulus repetitions on OSM. In visual crowding, the presentation of a physically identical stimulus to the target reduces crowding and improves target perception, whereas in spatial repetition blindness, the presentation of a stimulus that belongs to the same category (type) as the target impairs perception. Across two experiments, we found an interaction between spatial repetition blindness and OSM, such that repeating a same-type stimulus as the target increased masking magnitude relative to presentation of a different-type stimulus. These results are discussed in the context of the formation of object files. Moreover, the fact that the inducer only had to belong to the same "type" as the target in order to exacerbate masking, without necessarily being physically identical to the target, has important implications for our understanding of OSM per se. That is, our results show the target is processed to a categorical level in OSM despite effective masking and, strikingly, demonstrate that this category-level content directly influences whether or not the target is perceived, not just performance on another task (as in priming).

The ability to automatically detect changes in the environment is crucial for organisms to survive. In the visual system, changes in visual stimuli may evoke visual mismatch negativity (vMMN), an event-related potential (ERP) component that reflects automatic change detection. Previous studies that used visual masking to examine the effects of consciousness did not yield evidence that vMMN could be elicited by subliminal stimuli. However, these studies used relatively simple visual features. To further examine the role of consciousness in vMMN, the present study used emotional (happy and fearful) faces, which are biologically and socially significant visual stimuli. A passive oddball paradigm was employed, and we found that only fearful faces could evoke vMMN at a low consciousness level. Furthermore, the fear-related vMMN was enhanced by the consciousness level, and localized in regions of the brain associated with emotional face processing and the prefrontal cortex. We also found that the emotional visual mismatch oscillatory responses (vMORs) were associated with the enhancement of the alpha-band oscillation. Moreover, consciousness could weaken the happiness-related vMOR. These results suggested that changes to emotional faces-especially fearful faces-could be unconsciously detected by the brain. More importantly, this automatic change detection mechanism could be modulated by consciousness.

Recent visual masking studies that have measured visual awareness with graded subjective scales have often failed the show any evidence for unconscious visual processing in normal observers in a paradigm similar to that used in studies on blindsight patients. Without any reported awareness of the target, normal observers typically cannot discriminate target's features better than chance. The present study examined processing of color and orientation by measuring graded awareness and forced-choice discriminations for both features in each trial. When no awareness for either feature was reported, discrimination of each feature succeed better than expected by chance, even when the other feature was incorrectly discriminated in the same trial. However, the characteristics of the mask determined whether or not masked blindsight was observed. We conclude that when the processing channels are free from intra-channel interference, unbound or weakly bound features can guide behaviour without any reported awareness in normal observers.

We aimed to distinguish electrophysiological signatures of visual awareness from other task-related processes through manipulating the level of processing of visual stimuli. During an event-related EEG experiment, 36 subjects performed either color (low-level condition) or magnitude (high-level condition) evaluations of masked digits. Participants also assessed subjective visibility of each stimulus using the Perceptual Awareness Scale (PAS). Mean amplitude of the components of interest was analyzed (VAN − 140–240 ms; LP − 380–480 ms) with weighted regression mixed model. In the VAN component time window the mean amplitude correlated with PAS rating in both conditions. Mean amplitude in the LP time window correlated with PAS ratings in the high-level condition, but not in the low-level condition. Our results support the temporal unfolding of ERP makers of conscious processing, with an early component reflecting the initial perceptual experience and a late component being a correlate of the conscious experience of non-perceptual information., SCOPUS: ar.j, info:eu-repo/semantics/published

Object identification is driven, in part, by the extent to which we have sensorimotor experience with the object. Importantly, the activation of embodied object representations depends on contextual information. In the present study, we use a visual masking paradigm to investigate how the availability of visual information modulates the role of manipulability in the representation of object concepts. Using both an object naming task (i.e., linguistic response) and a picture-word matching task (i.e., manual response), we provide evidence that structural manipulability (the ability to pick up an object with one hand) and functional manipulability (the action information that pertains to the ultimate use of the object) have dissociable effects on object identification. In both tasks, the effects of structural manipulability were greater when structural information was available in the image (i.e., when the objects were unmasked); in contrast, the effects of functional manipulability were greater when the objects were masked. Importantly, these effects were not due to object familiarity or the age at which the name of the objects was acquired. Our results are consistent with the activation of the two pathways within the dorsal visual stream that are part of a distributed neural network that represents embodied action information. We extend previous research by showing that visual information determines which type of embodied information drives object identification. (PsycINFO Database Record (c) 2018 APA, all rights reserved).

When about half a century ago masking research emerged as one of the hot topics in psychophysics, cognitive psychology and psychophysiology, Bruce Bridgeman was among the leaders in this domain. His studies and papers on masking must not be overlooked also today. This article brings to the readers a brief review of Bridgeman's contributions to the field and directly related research from other laboratories, with an eye on the implications for consciousness studies.

Numerous non-invasive experimental “blinding” methods exist for suppressing the phenomenal awareness of visual stimuli. Not all of these suppressive methods occur at, and thus index, the same level of unconscious visual processing. This suggests that a functional hierarchy of unconscious visual processing can in principle be established. The empirical results of extant studies that have used a number of different methods and additional reasonable theoretical considerations suggest the following tentative hierarchy. At the highest levels in this hierarchy is unconscious processing indexed by object-substitution masking. The functional levels indexed by crowding, the attentional blink (and other attentional blinding methods), backward pattern masking, metacontrast masking, continuous flash suppression, sandwich masking, and single-flash interocular suppression, fall at progressively lower levels, while unconscious processing at the lowest levels is indexed by eye-based binocular-rivalry suppression. Although unconscious processing levels indexed by additional blinding methods is yet to be determined, a tentative placement at lower levels in the hierarchy is also given for unconscious processing indexed by Troxler fading and adaptation-induced blindness, and at higher levels in the hierarchy indexed by attentional blinding effects in addition to the level indexed by the attentional blink. The full mapping of levels in the functional hierarchy onto cortical activation sites and levels is yet to be determined. The existence of such a hierarchy bears importantly on the search for, and the distinctions between, neural correlates of conscious and unconscious vision.

This article explores the visual information used to categorize stimuli drawn from a common stimulus space into verbal and nonverbal categories using 2 experiments. Experiment 1 explores the effect of target duration on verbal and nonverbal categorization using backward masking to interrupt visual processing. With categories equated for difficulty for long and short target durations, intermediate target duration shows an advantage for verbal categorization over nonverbal categorization. Experiment 2 tests whether the results of Experiment 1 can be explained by shorter target duration resulting in a smaller signal-to-noise ratio of the categorization stimulus. To test for this possibility, Experiment 2 used integration masking with the same stimuli, categories, and masks as Experiment 1 with a varying level of mask opacity. As predicted, low mask opacity yielded similar results to long target duration while high mask opacity yielded similar results to short target duration. Importantly, intermediate mask opacity produced an advantage for verbal categorization over nonverbal categorization, similar to intermediate target duration. These results suggest that verbal and nonverbal categorization are affected differently by manipulations affecting the signal-to-noise ratio of the stimulus, consistent with multiple-system theories of categorizations. The results further suggest that verbal categorization may be more digital (and more robust to low signal-to-noise ratio) while the information used in nonverbal categorization may be more analog (and less robust to lower signal-to-noise ratio). This article concludes with a discussion of how these new results affect the use of masking in perceptual categorization and multiple-system theories of perceptual category learning.

Due to the movements of the observer and those of objects in the environment, retinotopic representations are highly unstable during ecological viewing conditions. The phenomenal stability of our perception suggests that retinotopic representations are transformed into non-retinotopic representations. It remains to show, however, which visual processes operate under retinotopic representations and which ones operate under non-retinotopic representations. Visual masking refers to the reduced visibility of one stimulus, called the target, due to the presence of a second stimulus, called the mask. Masking has been used extensively to study the dynamic aspects of visual perception. Previous studies using Saccadic Stimulus Presentation Paradigm (SSPP) suggested both retinotopic and non-retinotopic bases for visual masking. In order to understand how the visual system deals with retinotopic changes induced by moving targets, we investigated the retinotopy of visual masking and the fate of masked targets under conditions that do not involve eye movements. We have developed a series of experiments based on a radial Ternus-Pikler display. In this paradigm, the perceived Ternus-Pikler motion is used as a non-retinotopic reference frame to pit retinotopic against non-retinotopic visual masking hypothesis. Our results indicate that both metacontrast and structure masking are retinotopic. We also show that, under conditions that allow observers to read-out effectively non-retinotopic feature attribution, the target becomes visible at a destination different from its retinotopic/spatiotopic location. We discuss the implications of our findings within the context of ecological vision and dynamic form perception.

In object substitution masking (OSM) a surrounding mask (typically comprising of 4 dots) onsets with a target but lingers after offset; under such conditions, the ability to perceive the target can be significantly reduced. OSM was originally claimed to occur only when a target was not the focus of attention, for instance, when embedded in an array of distractors (Di Lollo, Enns, & Rensink, 2000). It was argued that the distractors influenced the time taken for focal attention to reach the target. Some recent work, however, failed to find any such distractor influence; the effect of mask duration was found to be independent of set size when steps were taken to avoid ceiling effects in the smallest set size condition (Argyropoulos, Gellatly, Pilling, & Carter, 2013; Filmer, Mattingley, & Dux, 2014). In 3 experiments, we repeatedly found that set size manipulations can interact with mask duration (in which neither ceiling nor floor effects are evident), with the effect of the mask on target perceptibility being amplified according to the number of distractor items. However, a further experiment (Experiment 4) showed that crowding by nearby distractors was actually responsible for this "set size" effect. When decoupled from crowding, set size alone did not interact with masking, though it did influence overall accuracy. Thus, the presence of distractors does influence OSM, but not in the way originally assumed by Di Lollo and colleagues in their model. The Crowding × OSM interaction suggests that the 2 phenomena involve partly overlapping mechanisms.

A central assumption of models proposed to explain object substitution masking (OSM) is that the phenomenon arises only when attention is distributed across several possible target locations. However, recent work has questioned the role of attention in OSM, suggesting instead that ceiling effects might explain the apparent interaction between spatial attention and masking. Here the authors report definitive evidence that OSM does not depend upon attention being distributed over space or time. In 2 experiments, they demonstrate reliable OSM for constant, foveal presentations of a single target stimulus. Crucially, in their design participants’ attention was always focused on the target, thus discounting the hypothesis that a key requirement for OSM is distributed attention. The findings challenge how OSM is conceptualized in the broader masking literature and have important implications for theories of visual processing.

Object-substitution masking (OSM) refers to when the delayed disappearance of a sparse mask that spatially surrounds but does not overlap the target impairs target perception. Two major theoretical accounts have been offered to explain OSM: the object-substitution account, which stipulates that masking occurs when a separate mask representation replaces the target, and the object-updating account, which espouses that masking is the product of a single representation initially containing information about the target that is modified to reflect the mask. Here I critically review the evidence that has accumulated over two decades for the two models, and find the evidence overwhelmingly in favor of the object-updating account. This object-updating account places OSM in the larger framework of related phenomena such as a repetition blindness, apparent motion, and object correspondence through occlusion that gauge how the visual system assigns episodic object representations in the face of dynamic and ambiguous input. Implications for visual cognition more broadly are discussed. (PsycINFO Database Record

Conscious detection and discrimination of a visual target stimulus can be prevented by the presentation a spatially nonoverlapping, but temporally trailing, visual masking stimulus. This phenomenon, known as object substitution masking (OSM), has long been associated with spatial attention, with diffuse attention seemingly being key for the effect to be observed. Recently, this hypothesis has been questioned. We sought to provide a definitive test of the involvement of spatial attention in OSM by using an eight-alternative forced choice task under a range of mask durations, set sizes, and target/distractor spatial configurations. The results provide very little evidence that set size, and thus the distribution of spatial attention, interacts with masking magnitude. These findings have implications for understanding the mechanisms underlying OSM and the relationship between consciousness and attention.

Viewers can rapidly extract a holistic semantic representation of a real-world scene within a single eye fixation, an ability called recognizing the gist of a scene, and operationally defined here as recognizing an image's basic-level scene category. However, it is unknown how scene gist recognition unfolds over both time and space-within a fixation and across the visual field. Thus, in 3 experiments, the current study investigated the spatiotemporal dynamics of basic-level scene categorization from central vision to peripheral vision over the time course of the critical first fixation on a novel scene. The method used a window/scotoma paradigm in which images were briefly presented and processing times were varied using visual masking. The results of Experiments 1 and 2 showed that during the first 100 ms of processing, there was an advantage for processing the scene category from central vision, with the relative contributions of peripheral vision increasing thereafter. Experiment 3 tested whether this pattern could be explained by spatiotemporal changes in selective attention. The results showed that manipulating the probability of information being presented centrally or peripherally selectively maintained or eliminated the early central vision advantage. Across the 3 experiments, the results are consistent with a zoom-out hypothesis, in which, during the first fixation on a scene, gist extraction extends from central vision to peripheral vision as covert attention expands outward.

A visual search for targets is facilitated when the target objects are on a different depth plane than other masking objects cluttering the scene. The ability of observers to determine whether one of four letters presented stereoscopically at four symmetrically located positions on the fixation plane differed from the other three was assessed when the target letters were masked by other randomly positioned and oriented letters appearing on the same depth plane as the target letters, or in front, or behind it. Three additional control maskers, derived from the letter maskers, were also presented on the same three depth planes: (1) random-phase maskers (same spectral amplitude composition as the letter masker but with the phase spectrum randomized); (2) random-pixel maskers (the locations of the letter maskers’ pixel amplitudes were randomized); (3) letter-fragment maskers (the same letters as in the letter masker but broken up into fragments). Performance improved with target duration when the target-letter plane was in front of the letter-masker plane, but not when the target letters were on the same plane as the masker, or behind it. A comparison of the results for the four different kinds of maskers indicated that maskers consisting of recognizable objects (letters or letter fragments) interfere more with search and comparison judgments than do visual noise maskers having the same spatial frequency profile and contrast. In addition, performance was poorer for letter maskers than for letter-masker fragments, suggesting that the letter maskers interfered more with performance than the letter-fragment maskers because of the lexical activity they elicit.

Previous studies [Marcel, A. J. (1983). Conscious and unconscious perception: Experiments on visual masking and word recognition. Cognitive Psychology, 15(2), 197-237; Wentura, D., & Frings, C. (2005). Repeated masked category primes interfere with related exemplars: New evidence for negative semantic priming. Journal of Experimental Psychology: Learning, Memory, and Cognition, 31(1), 108-120] suggested that repeatedly presenting a masked stimulus improves priming without increasing perceptual awareness. However, neural theories of consciousness predict the opposite: Increasing bottom-up strength in such a paradigm should also result in increasing availability to awareness. Here, we tested this prediction by manipulating the number of repetitions of a strongly masked digit. Our results do not replicate the dissociation observed in previous studies and are instead suggestive that repeating an unconscious and attended masked stimulus enables the progressive emergence of perceptual awareness.

Conscious and unconscious cognitive processes contribute independently to human behavior and can be dissociated. For example, humans report failing to see objects clearly in the periphery while simultaneously being able to grasp those objects accurately (Milner in Proc R Soc B Biol Sci 279:2289-2298, 2012). Knowing whether similar dissociations are present in nonverbal species is critical to our understanding of comparative psychology and the evolution of brains. However, such dissociations are difficult to detect in nonhumans because verbal reports of experience are the main way we discriminate putative conscious from unconscious processing. We trained monkeys in a localization task in which they responded to the location where a target appeared, and a matched detection task in which they reported the presence or absence of the same target. We used masking to manipulate the visibility of targets. Accuracy was high in both tasks when stimuli were unmasked and was attenuated by visual masking. At the strongest level of masking, performance in the detection task was at chance, while localization remained significantly above chance. Critically, errors in the detection task were predominantly misses, indicating that the monkeys' behavior remained under stimulus control, but that the monkeys did not detect the target despite above-chance localization. While these results cannot establish the existence of phenomenal vision in monkeys, the dissociation of visually guided action from detection parallels the dissociation of conscious and unconscious vision seen in humans.

We introduce a new version of the perceptual retouch model. This model was used for explaining properties of temporal interaction of successive objects in reaching conscious representation. The new model incorporates two interactive binding operations – binding features for objects and binding the bound feature-objects with a large scale oscillatory system that corresponds to perceptual consciousness. Here, the typical result of masking experiments – second object advantage in conscious perception – is achieved by applying the effects of a common synchronizing oscillator with a delay. This delayed modulation of each of the feature-binding first-order oscillators that represent emerging and decaying neural activities of each of the objects guarantees that the oscillating synchrony of the feature-neurons of the following object is higher than the synchrony of the feature-neurons of the first presented object. Thus we model the fact that the following object dominates the preceding object in conscious perception. We also show the capacity of the model to simulate illusory misbinding of features from different objects. The third qualitative effect, the relative release of the first object from backward masking is achieved by priming the non-specific oscillatory modulation ahead in time.

article i nfo Article history: Performance in spatial cueing tasks is characterized by a rapid attentional enhancement with increasing cue- target SOA. We recently found that this enhancement function also applies when the cue and the target are presented invariably at a single central location, suggesting a universal cueing time course (Wilschut et al., 2011, PLoS ONE, 6, e27661). However, using a very similar cueing task, Nieuwenstein et al. (2009, JoV, 9, 1-14) have found a rather different pattern, namely a U-shaped deficit in performance after a cue-like stim- ulus. The present study varied the properties of the cue and the target in order to investigate the mechanisms underlying the different time functions. In four experiments, cueing was found to either improve or decrease performance with increasing SOA, depending on the type of target that was used. In addition, the level of per- formance at the shortest cue-target intervals (33-83 ms) was dependent on the relative strength of the cue and the target, akin to what has been found in visual masking studies. The results suggest that cueing shapes performance via two mechanisms, one sensory-related and one attention-related, the combination of which results in either U-shaped or monotonic patterns.

According to the levels-of-processing hypothesis, transitions from unconscious to conscious perception may depend on stimulus processing level, with more gradual changes for low-level stimuli and more dichotomous changes for high-level stimuli. In an event-related fMRI study we explored this hypothesis using a visual backward masking procedure. Task requirements manipulated level of processing. Participants reported the magnitude of the target digit in the high-level task, its color in the low-level task, and rated subjective visibility of stimuli using the Perceptual Awareness Scale. Intermediate stimulus visibility was reported more frequently in the low-level task, confirming prior behavioral results. Visible targets recruited insulo-fronto-parietal regions in both tasks. Task effects were observed in visual areas, with higher activity in the low-level task across all visibility levels. Thus, the influence of level of processing on conscious perception may be mediated by attentional modulation of activity in regions representing features of consciously experienced stimuli.

The human visual system has the remarkable ability to rapidly detect meaning from visual stimuli. Potter, Wyble, Hagmann, and McCourt (Attention, Perception, & Psychophysics, 76, 270-279, 2014) tested the minimum viewing time required to obtain meaning from a stream of pictures shown in a rapid serial visual presentation (RSVP) sequence containing either six or 12 pictures. They reported that observers could detect the presence of a target picture specified by name (e.g., smiling couple) even when the pictures in the sequence were presented for just 13 ms each. Potter et al. claimed that this was insufficient time for feedback processing to occur, so feedforward processing alone must be able to generate conscious awareness of the target pictures. A potential confound in their study is that the pictures in the RSVP sequence sometime contained areas with no high-contrast edges, and so may not have adequately masked each other. Consequently, iconic memories of portions of the target pictures may have persisted in the visual system, thereby increasing the effective presentation time. Our study addressed this issue by redoing the Potter et al. study, but using four different types of masks. We found that when adequate masking was used, no evidence emerged that observers could detect the presence of a specific target picture, even when each picture in the RSVP sequence was presented for 27 ms. On the basis of these findings, we cannot rule out the possibility that feedback processing is necessary for individual pictures to be recognized.

Practice can enhance of perceptual sensitivity, a well-known phenomenon called perceptual learning. However, the effect of practice on subjective perception has received little attention. We approach this problem from a visual psychophysics and computational modeling perspective. In a sequence of visual search experiments, subjects significantly increased the ability to detect a "trained target". Before and after training, subjects performed two psychophysical protocols that parametrically vary the visibility of the "trained target": an attentional blink and a visual masking task. We found that confidence increased after learning only in the attentional blink task. Despite large differences in some observables and task settings, we identify common mechanisms for decision-making and confidence. Specifically, our behavioral results and computational model suggest that perceptual ability is independent of processing time, indicating that changes in early cortical representations are effective, and learning changes decision criteria to convey choice and confidence.

Self-relevant information is prioritized in processing. Some have suggested the mechanism driving this advantage is akin to the automatic prioritization of physically salient stimuli in information processing (Humphreys & Sui, 2015). Here we investigate whether self-relevant information is prioritized for awareness under continuous flash suppression (CFS), as has been found for physical salience. Gabor patches with different orientations were first associated with the labels You or Other. Participants were more accurate in matching the self-relevant association, replicating previous findings of self-prioritization. However, breakthrough into awareness from CFS did not differ between self- and other-associated Gabors. These findings demonstrate that self-relevant information has no privileged access to awareness. Rather than modulating the initial visual processes that precede and lead to awareness, the advantage of self-relevant information may better be characterized as prioritization at later processing stages.

In metacontrast masking target visibility is modulated by the time until a masking stimulus appears. The effect of this temporal delay differs across participants in such a way that individual human observers’ performance shows distinguishable types of masking functions which remain largely unchanged for months. Here we examined whether individual differences in masking functions depend on different response criteria in addition to differences in discrimination sensitivity. To this end we reanalyzed previously published data and conducted a new experiment for further data analyses. Our analyses demonstrate that a distinction of masking functions based on the type of masking stimulus is superior to a distinction based on the target–mask congruency. Individually different masking functions are based on individual differences in discrimination sensitivities and in response criteria. Results suggest that individual differences in metacontrast masking result from individually different criterion contents.

Anxiety has been associated with enhanced unconscious processing of threat and attentional biases towards threat. Here, we focused on the phenomenology of perception in anxiety and examined whether threat-related material more readily enters anxious than non-anxious individuals’ awareness. In six experiments, we compared the stimulus exposures required for each anxiety group to become objectively or subjectively aware of masked facial stimuli varying in emotional expression. Crucially, target emotion was task irrelevant. We found that high trait-anxiety individuals required less sensory evidence (shorter stimulus exposure times) to become aware of the face targets. This anxiety-based difference was observed for fearful faces in all experiments, but with non-threat faces, it emerged only when these were presented among threatening faces. Our findings suggest a prominent role for affective context in high-anxiety individuals’ conscious perception of visual stimuli. Possible mechanisms underlying the influence of context in lowering awareness thresholds in anxious individuals are discussed.

Visual attention has temporal limitations. In the attentional blink (AB) a stream of stimuli such as letters or digits are presented to a participant on a computer monitor at a rapid rate. Embedded in the stream are two targets that the participant must try to identify. Identification of the second target is severely impaired if it is presented within approximately 500. ms of the first target. This is the 'blink' in visual attention. In this study we examined the role of the magnocellular visual pathway in the AB. This fast conducting pathway has high temporal resolution and contrast sensitivity. It is also insensitive to the direction of chromatic contrast, and this attribute was exploited in order to isolate its contributions to temporal attention. Colour defined, luminance noise masked AB streams were compared to AB streams of varying achromatic contrast. The four observers, (2F and 2M) aged between 21 and 35. years, had normal visual acuity and colour vision. The colour stimuli produced a similar blink to the moderate contrast achromatic stimuli. This indicates that the magnocellular pathway does not have a privileged role in the attentional blink. We provide an explanation of previous apparently contradictory findings in terms of the role of different types of visual masking in the attentional blink. © 2011 Elsevier Inc.

Visual masking and visual suppression by transcranial magnetic stimulation (TMS) are both widely utilized in cognitive neuroscience to investigate a wide range of processes. However, the neural processes affected by visual masking and TMS remain unclear. We compared para- and metacontrast masking with TMS-induced suppression of visibility in a within-subjects design where participants were asked to detect and rate the visibility of a stimulus. TMS pulses applied 75–109 msec after the onset of the visual stimulus reduced the subjective visibility of the target. Even when the TMS pulses completely eliminated the conscious perception of the target, unconscious location detection was possible. The visual masking condition yielded similar results: metacontrast did not eliminate unconscious location detection even when the target was reported not seen at all. As the first target-related signals were likely to reach the visual cortex before TMS pulses started to modulate target visibility, we suggest that TMS and metacontrast masking affected neural signals subsequent to the target’s transient onset-response. This implies that a preserved onset-response is sufficient for unconscious processing of stimulus attributes, but not for conscious perception.

Visual masking of primes lowers prime visibility but spares processing of primes as reflected in prime–target congruence and prime–response compatibility effects. However, the question is how to appropriately measure prime visibility. Here, we tested the influence of three procedural variables on prime visibility measures: prime–target similarity, prime–response similarity, and the variability of prime–response mappings. Our results show that a low prime–target similarity is a favorable condition for a prime visibility measure because it increases the sensitivity of this measure in comparison to a high prime–target similarity.

In object substitution masking (OSM) a sparse, temporally trailing 4-dot mask impairs target identification, even though it has different contours from, and does not spatially overlap with the target. Here, we demonstrate a previously unknown characteristic of OSM: Observers show reduced masking at prolonged (e.g., 640 ms) relative to intermediate mask durations (e.g., 240 ms). We propose that with prolonged exposure, the mask's visual representation is consolidated, which allows processing of the lingering target icon to be reinitiated, thereby improving performance. Our findings suggest that when the visual system is confronted with 2 temporally contiguous stimuli, although one may initially gain access to consciousness above the other, the "losing" stimulus is not irreversibly lost to awareness.