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Hysteresis is a well-known phenomenon in physics that relates changes in a system with its prior history. It is also part of human visual experience (perceptual hysteresis), and two different neural mechanisms might explain it: persistence (a cause of positive hysteresis), which forces to keep a current percept for longer, and adaptation (a cause of negative hysteresis), which in turn favors the switch to a competing percept early on. In this study, we explore the neural correlates underlying these mechanisms and the hypothesis of their competitive balance, by combining behavioral assessment with fMRI. We used machine learning on the behavioral data to distinguish between positive and negative hysteresis, and discovered a neural correlate of persistence at a core region of the ventral attention network, the anterior insula. Our results add to the understanding of perceptual multistability and reveal a possible mechanistic explanation for the regulation of different forms of perceptual hysteresis. •Two mechanisms may help explain the hysteresis phenomenon in human visual experience: adaptation and persistence.•We found evidence for a continuous competition between these perceptual history mechanisms, together with a stronger involvement of the anterior insula when persistence dominated.•Our results support the hypothesis of differential brain network recruitment for the two mechanisms and provide further insight into the underlying causes of hysteresis in multistable perception.

Visual adaptation describes the processes by which the visual system alters its operating properties in response to changes in the environment. It is one of the mechanisms controlling visual perceptual bistability – when two perceptual solutions are available – by controlling the duration of each percept. Moving plaids are an example of such ambiguity. They can be perceived as two surfaces sliding incoherently over each other or as a single coherent surface. Here, we investigated, using fMRI, whether activity in the human motion complex (hMT+), a region tightly related to the perceptual integration of visual motion, is modulated by distinct forms of visual adaptation to coherent or incoherent perception of moving plaids. Our hypothesis is that exposure to global coherent or incoherent moving stimuli leads to different levels of measurable adaptation, reflected in hMT+ activity. We found that the strength of the measured visual adaptation effect depended on whether subjects integrated (coherent percept) or segregated (incoherent percept) surface motion signals. Visual motion adaptation was significant both for coherent motion and globally incoherent surface motion. Although not as strong as to the coherent percept, visual adaptation due to the incoherent percept also affects hMT+. This shows that adaptation can contribute to regulate percept duration during visual bistability, with distinct weights, depending on the type of percept. Our findings suggest a link between bistability and adaptation mechanisms, both due to coherent and incoherent motion percepts, but in an asymmetric manner. These asymmetric adaptation weights have strong implications in models of perceptual decision and may explain asymmetry of perceptual interpretation periods. •Perceptual adaptation occurs for both coherent and incoherent moving surfaces.•Adaptation mechanisms due to coherent and incoherent moving surfaces are asymmetric.•Asymmetric adaptation weights may explain imbalances in bistable perception.

A growing body of literature suggests that feedback modulation of early visual processing is ubiquitous and central to cortical computation. In particular stimuli with high-level content that invariably activate ventral object responsive regions have been shown to suppress early visual cortex. This suppression was typically interpreted in the framework of predictive coding and feedback from ventral regions. Here we examined early visual modulation during perception of a bistable Gestalt illusion that has previously been shown to be mediated by dorsal parietal cortex rather than by ventral regions that were not activated. The bistable dynamic stimulus consisted of moving dots that could either be perceived as corners of a large moving cube (global Gestalt) or as distributed sets of locally moving elements. We found that perceptual binding of local moving elements into an illusory Gestalt led to spatially segregated differential modulations in both, V1 and V2: representations of illusory lines and foreground were enhanced, while inducers and background were suppressed. Furthermore, correlation analyses suggest that distinct mechanisms govern fore- and background modulation. Our results demonstrate that motion-induced Gestalt perception differentially modulates early visual cortex in the absence of ventral stream activation. •We used a bistable Gestalt illusion to examine feedback modulations in V1 and V2.•The Gestalt perception has been shown to be mediated by dorsal cortex.•Representations of inducers, fore- and back-ground were differentially modulated.•Correlation analyses suggest distinct sub-processes underlying the modulations.•Our results are in line with predictive coding accounts of visual processing.

The phenomenon of bistable perception, in which perception alternates spontaneously despite constant sensory stimulation, has been particularly useful in probing the neural bases of conscious perception. The study of such bistability requires access to the observer's perceptual dynamics, which is usually achieved via active report. This report, however, constitutes a confounding factor in the study of conscious perception and can also be biased in the context of certain experimental manipulations. One approach to circumvent these problems is to track perceptual alternations using signals from the eyes or the brain instead of observers' reports. Here we aimed to optimize such decoding of perceptual alternations by combining eye and brain signals. Eye-tracking and functional magnetic resonance imaging (fMRI) was performed in twenty participants while they viewed a bistable visual plaid motion stimulus and reported perceptual alternations. Multivoxel pattern analysis (MVPA) for fMRI was combined with eye-tracking in a Support vector machine to decode participants' perceptual time courses from fMRI and eye-movement signals. While both measures individually already yielded high decoding accuracies (on average 86% and 88% correct, respectively) classification based on the two measures together further improved the accuracy (91% correct). These findings show that leveraging on both fMRI and eye movement data may pave the way for optimized no-report paradigms through improved decodability of bistable motion perception and hence for a better understanding of the neural correlates of consciousness. •Bistable plaid motion perception was decoded from eye and brain signals.•Combining data from eye tracking and fMRI achieved very high decoding accuracies.•The proposed experimental setup and analysis will help improving no-report paradigms.

Transcutaneous vagus nerve stimulation (tVNS) is widely used for clinical applications, but its mechanism of action is poorly understood. One candidate pathway that might mediate the effects of tVNS is an increase in GABAergic neurotransmission. In this study, we investigated the effect of tVNS on visual bistable perception, which is highly coupled to GABA. Participants were 34 healthy young subjects. We used a static (Necker cube) and a dynamic (structure from motion) bistable perception task. Each subject underwent tVNS as well as sham (placebo) stimulation for ∼45 min. We analyze effects of tVNS on percept durations by means of Bayesian multilevel regression. We find no evidence for a modulation of bistable perception dynamics through tVNS in either task, but the analyses do not ultimately confirm the null hypothesis either. We discuss different possible implications of our finding and propose that GABAergic effects of tVNS should be further investigated using more direct measures of GABA concentration, and, more generally, that a better understanding of the mechanisms of action of vagus nerve stimulation is needed. Finally, we discuss limitations of our study design, data analysis, and conclusions.

Visual images consisting of repetitive patterns can elicit striking illusory motion percepts. For almost 200 years, artists, psychologists, and neuroscientists have debated whether this type of illusion originates in the eye or in the brain. For more than a decade, the controversy has centered on the powerful illusory motion perceived in the painting Enigma, created by op-artist Isia Leviant. However, no previous study has directly correlated the Enigma illusion to any specific physiological mechanism, and so the debate rages on. Here, we show that microsaccades, a type of miniature eye movement produced during visual fixation, can drive illusory motion in ENIGMA: We asked subjects to indicate when illusory motion sped up or slowed down during the observation of Enigma while we simultaneously recorded their eye movements with high precision. Before \"faster\" motion periods, the rate of microsaccades increased. Before \"slower/no\" motion periods, the rate of microsaccades decreased. These results reveal a direct link between microsaccade production and the perception of illusory motion in Enigma and rule out the hypothesis that the origin of the illusion is purely cortical.

The posterior parietal cortex (PPC) is understood to be active when observers perceive three-dimensional (3D) structure. However, it is not clear how central this activity is in the construction of 3D spatial representations. Here, we examine whether PPC is essential for two aspects of visual depth perception by testing patients with lesions affecting this region. First, we measured subjects' ability to discriminate depth structure in various 3D surfaces and objects using binocular disparity. Patients with lesions to right PPC (N = 3) exhibited marked perceptual deficits on these tasks, whereas those with left hemisphere lesions (N = 2) were able to reliably discriminate depth as accurately as control subjects. Second, we presented an ambiguous 3D stimulus defined by structure from motion to determine whether PPC lesions influence the rate of bistable perceptual alternations. Patients' percept durations for the 3D stimulus were generally within a normal range, although the two patients with bilateral PPC lesions showed the fastest perceptual alternation rates in our sample. Intermittent stimulus presentation reduced the reversal rate similarly across subjects. Together, the results suggest that PPC plays a causal role in both inferring and maintaining the perception of 3D structure with stereopsis supported primarily by the right hemisphere, but do not lend support to the view that PPC is a critical contributor to bistable perceptual alternations. This article is part of the themed issue ‘Vision in our three-dimensional world’.

The integration of local moving elements into a unified gestalt percept has previously been linked to the posterior parietal cortex. There are two possible interpretations for the lack of involvement of other occipital regions. The first is that parietal cortex is indeed uniquely functionally specialized to perform grouping. Another possibility is that other visual regions can perform grouping as well, but that the large spatial separation of the local elements used previously exceeded their neurons' receptive field (RF) sizes, preventing their involvement. In this study we distinguished between these two alternatives. We measured whole-brain activity using fMRI in response to a bistable motion illusion that induced mutually exclusive percepts of either an illusory global Gestalt or of local elements. The stimulus was presented in two sizes, a large version known to activate IPS only, and a version sufficiently small to fit into the RFs of mid-level dorsal regions such as V5/MT. We found that none of the separately localized motion regions apart from parietal cortex showed a preference for global Gestalt perception, even for the smaller version of the stimulus. This outcome suggests that grouping-by-motion is mediated by a specialized size-invariant mechanism with parietal cortex as its anatomical substrate. •Prior work has shown a causal role of parietal cortex in spatial grouping.•The use of large stimuli may have limited cortical involvement to parietal cortex.•Here we tested involvement of mid-level regions in binding with small stimuli.•Results show that only parietal cortex, not earlier visual regions, mediate binding.•This suggests that uniquely parietal cortex mediates size-invariant grouping.

When multistable displays—stimuli that are compatible with several comparably likely perceptual interpretations—are presented intermittently, the perceptual state at the stimulus onset shows a complex dependence on the duration of the preceding blank interval. Specifically, perception is maximally destabilized for interruptions that are approximately 500 ms long, but it is stabilized by the use of shorter or longer blank intervals. This nonmonotonic dependence of perceptual stability on the blank interval duration raises questions about a number of history effects that are involved and about their nature, including the underlying neural representations. One way to characterize history effects is by looking at their specificity to the change of display properties. Here we measured the shape specificity for perception of the kinetic-depth effect when interruptions were brief (50 ms). For this time interval, perception is thought to be stabilized by neural persistence, a lingering trace of the prior neural activity. We found that perceptual stability depended on the shapes of the objects presented both before and after the break, but not on the similarity between the objects. These results matched earlier reports of the shape specificity of neural adaptation (destabilizing aftereffect for blanks 200–800 ms long). However, our results were markedly different from the shape specificity of sensory memory of multistable perception (a stabilizing effect for blanks > 800–1,000 ms). We concluded that whereas neural persistence and adaptation both act on the same motion-selective neural representation, sensory memory depends on another, possibly partially overlapping, shape-selective neural ensemble.

Our brain constantly tries to anticipate the future by using a variety of memory mechanisms. Interestingly, studies using the intermittent presentation of multistable displays have shown little perceptual persistence for interruptions longer than a few hundred milliseconds. Here we examined whether we can facilitate the perceptual stability of bistable displays following a period of invisibility by employing a physically plausible and ecologically valid occlusion event sequence, as opposed to the typical intermittent presentation, with sudden onsets and offsets. To this end, we presented a bistable rotating structure-from-motion display that was moving along a linear horizontal trajectory on the screen and either was temporarily occluded by another object (a cardboard strip in Exp. 1 , a computer-generated image in Exp. 2 ) or became invisible due to eye closure (Exp. 3 ). We report that a bistable rotation direction reliably persisted following occlusion or interruption only (1) if the pre- and postinterruption locations overlapped spatially (an occluder with apertures in Exp. 2 or brief, spontaneous blinks in Exp. 3 ) or (2) if an object’s size allowed for the efficient grouping of dots on both sides of the occluding object (large objects in Exp. 1 ). In contrast, we observed no persistence whenever the pre- and postinterruption locations were nonoverlapping (large solid occluding objects in Exps. 1 and 2 and long, prompted blinks in Exp. 3 ). We report that the bistable rotation direction of a moving object persisted only for spatially overlapping neural representations, and that persistence was not facilitated by a physically plausible and ecologically valid occlusion event.