Mechanisms selectively engaged in rivalry: normal vision habituates, rivalrous vision primes

AbstractWhen rivalrous stimuli are presented intermittently, perception stabilises. This indicates the operation of perceptual memory across interruptions in stimulation. Here we show that a percept under non-rivalrous and rivalrous conditions has qualitatively different effects on subsequent rivalrous vision. When an image is perceived under rivalrous viewing, that image is more likely to be perceived in later rivalrous viewing: an effect of stabilisation or priming. When the same image is perceived under non-rivalrous viewing conditions, it is less likely to be perceived again during subsequent rivalrous viewing: an effect of adaptation or habituation. When these stimuli possess different attributes to those in subsequent vision their effect declines. This suggests that visual rivalry might recruit mechanisms that are not engaged in ‘normal’ non-rivalrous vision but perhaps dedicated to the resolution of competing sensory information

Orientation dependence of the orientation-contingent face aftereffect

AbstractProlonged exposure to upright and inverted female and male faces produces opposite effects on subsequent judgments of the sex of faces depending on their orientation. We show that the magnitude of this orientation-contingent gender aftereffect can be predicted from simple aftereffects induced separately at the same orientations. The contingent aftereffect can also be induced in faces tilted 90° to the right and left, eliminating any difference in face-processing strategy that may be in operation with upright and inverted faces. This suggests that neurons employing a single face encoding strategy can be activated in an orientation-specific manner

The timecourse of higher-level face aftereffects

AbstractPerceptual aftereffects for simple visual attributes processed early in the cortical hierarchy increase logarithmically with adapting duration and decay exponentially with test duration. This classic timecourse has been reported recently for a face identity aftereffect [Leopold, D. A., Rhodes, G., Müller, K.-M., & Jeffery, L. (2005). The dynamics of visual adaptation to faces. Proceedings of the Royal Society of London, Series B, 272, 897–904], suggesting that the dynamics of visual adaptation may be similar throughout the visual system. An alternative interpretation, however, is that the classic timecourse is a flow-on effect of adaptation of a low-level, retinotopic component of the face identity aftereffect. Here, we examined the timecourse of the higher-level (size-invariant) components of two face aftereffects, the face identity aftereffect and the figural face aftereffect. Both showed the classic pattern of logarithmic build-up and exponential decay. These results indicate that the classic timecourse of face aftereffects is not a flow-on effect of low-level retinotopic adaptation, and support the hypothesis that dynamics of visual adaptation are similar at higher and lower levels of the cortical visual hierarchy. They also reinforce the perceptual nature of face aftereffects, ruling out demand characteristics and other post-perceptual factors as plausible accounts

Improving visual sensitivity with subthreshold transcranial magnetic stimulation

We probed for improvement of visual sensitivity in human participants using transcranial magnetic stimulation (TMS). Stimulation of visual cortex can induce an illusory visual percept known as a phosphene. It is known that TMS, delivered at intensities above the threshold to induce phosphenes, impairs the detection of visual stimuli. We investigated how the detection of a simple visual stimulus is affected by TMS applied to visual cortex at or below the phosphene threshold. Participants performed the detection task while the contrast of the visual stimulus was varied from trial to trial according to an adaptive staircase procedure. Detection of the stimulus was enhanced when a single pulse of TMS was delivered to the contralateral visual cortex 100 or 120 ms after stimulus onset at intensities just below the phosphene threshold. No improvement in visual sensitivity was observed when TMS was applied to the visual cortex in the opposite hemisphere (ipsilateral to the visual stimulus). We conclude that TMS-induced neuronal activity can sum with stimulus-evoked activity to augment visual perception

Humans Have an Expectation That Gaze Is Directed Toward Them

This work is supported by the Australian Research Council Discovery Project (DP120102589) to C.C. and A.C. C.C. is supported by an Australian Research Council Future Fellowship (FT110100150). A.C. is supported by the Medical Research Council, UK (MC_US_A060_5PQ50)

Visual Perception: Ambiguity Involving Parietal Cortex

SummaryOur brain is constantly interpreting ambiguous sensory input to deliver a stable perceptual representation of the environment. Two new studies suggest that superior parietal cortex plays a causal role in resolving perceptual ambiguity. Ironically, their results are somewhat ambiguous as to what that role might be

Does cortical motion adaptation exhibit functional properties analogous to light adaptation in the retina?

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Aftereffect of adaptation to Glass patterns

AbstractOur visual systems constantly adapt their representation of the environment to match the prevailing input. Adaptation phenomena provide striking examples of perceptual plasticity and offer valuable insight into the mechanisms of sensory coding. Here, we describe an aftereffect of adaptation to a spatially structured image whereby an unstructured test stimulus takes on illusory structure locally perpendicular to that of the adaptor. Objective measurement of the strength of the aftereffect for different patterns suggests a neural locus of adaptation prior to the extraction of complex form in the visual processing hierarchy, probably at the level of primary visual cortex. This view is supported by further experiments showing that the aftereffect exhibits partial interocular transfer but complete transfer across opposite contrast polarities. However, the aftereffect does show weak position invariance, suggesting that adaptation at higher levels of the visual system may also contribute to the effect

Adaptation to temporal modulation can enhance differential speed sensitivity

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Fundamental mechanisms of visual motion detection: models, cells and functions

Taking a comparative approach, data from a range of visual species are discussed in the context of ideas about mechanisms of motion detection. The cellular basis of motion detection in the vertebrate retina, sub-cortical structures and visual cortex is reviewed alongside that of the insect optic lobes. Special care is taken to relate concepts from theoretical models to the neural circuitry in biological systems. Motion detection involves spatiotemporal pre-filters, temporal delay filters and non-linear interactions. A number of different types of non-linear mechanism such as facilitation, inhibition and division have been proposed to underlie direction selectivity. The resulting direction-selective mechanisms can be combined to produce speed-tuned motion detectors. Motion detection is a dynamic process with adaptation as a fundamental property. The behavior of adaptive mechanisms in motion detection is discussed, focusing on the informational basis of motion adaptation, its phenomenology in human vision, and its cellular basis. The question of whether motion adaptation serves a function or is simply the result of neural fatigue is critically addressed. Crow