Visual sensitivity and bias oscillate phase-locked to saccadic eye movements

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influence of saccadic adaptation on spatial localization comparison of verbal and pointing reports

Under conditions of short-term saccadic adaptation, stimuli presented long before saccadic onset are perceptually mislocalized in space. Here we study whether saccadic adaptation can also affect localization of objects by pointing. We measured localization performance during fixation and after normal saccades and adapted saccades, for a bar presented well before a saccadic eye movement, for both pointing and verbal localization, under open-loop conditions generated by a transient dark period about 300 ms after the presentation of the bar. During fixation and normal saccade, localization performance for verbal report was veridical, while for pointing there was an overestimation of the target eccentricity respect to gaze, in agreement with the idea of separate representations of space for action and perception. During saccadic adaptation, there was a significant shift of both pointing and verbal report localization in the direction of adaptation with similar spatial selectivity for both tasks. These results indicate that saccadic adaptation induces a similar re-calibration of the action map as well as of the perceptual map, suggesting a common site of operation in the transformation from eye-centered to gaze-centered coordinates

constructing stable spatial maps of the word

To interact rapidly and effectively with our environment, our brain needs access to a neural representation—or map—of the spatial layout of the external world. However, the construction of such a map poses major challenges to the visual system, given that the images on our retinae depend on where the eyes are looking, and shift each time we move our eyes, head, and body to explore the world. Much research has been devoted to how the stability is achieved, with the debate often polarized between the utility of spatiotopic maps (that remain solid in external coordinates), as opposed to transiently updated retinotopic maps. Our research suggests that the visual system uses both strategies to maintain stability. f MRI, motion-adaptation, and saccade-adaptation studies demonstrate and characterize spatiotopic neural maps within the dorsal visual stream that remain solid in external rather than retinal coordinates. However, the construction of these maps takes time (up to 500 ms) and attentional resources. To s..

Adaptation to size affects saccades with long but not short latencies

Maintained exposure to a specific stimulus property-such as size, color, or motion-induces perceptual adaptation aftereffects, usually in the opposite direction to that of the adaptor. Here we studied how adaptation to size affects perceived position and visually guided action (saccadic eye movements) to that position. Subjects saccaded to the border of a diamond-shaped object after adaptation to a smaller diamond shape. For saccades in the normal latency range, amplitudes decreased, consistent with saccading to a larger object. Short-latency saccades, however, tended to be affected less by the adaptation, suggesting that they were only partly triggered by a signal representing the illusory target position. We also tested size perception after adaptation, followed by a mask stimulus at the probe location after various delays. Similar size adaptation magnitudes were found for all probe-mask delays. In agreement with earlier studies, these results suggest that the duration of the saccade latency period determines the reference frame that codes the probe location

Binocular Rivalry Measured 2 Hours After Occlusion Therapy Predicts the Recovery Rate of the Amblyopic Eye in Anisometropic Children

Recent studies on adults have shown that short-term monocular deprivation boosts the deprived eye signal in binocular rivalry, reflecting homeostatic plasticity. Here we investigate whether homeostatic plasticity is present also during occlusion therapy for moderate amblyopia.PURPOSE. Recent studies on adults have shown that short-term monocular deprivation boosts the deprived eye signal in binocular rivalry, reflecting homeostatic plasticity. Here we investigate whether homeostatic plasticity is present also during occlusion therapy for moderate amblyopia. METHODS. Binocular rivalry and visual acuity (using Snellen charts for children) were measured in 10 children (mean age 6.2±6 1 years) with moderate anisometropic amblyopia before the beginning of treatment and at four intervals during occlusion therapy (2 hours, 1, 2, and 5 months). Visual stimuli were orthogonal gratings presented dichoptically through ferromagnetic goggles and children reported verbally visual rivalrous perception. Bangerter filters were applied on the spectacle lens over the best eye for occlusion therapy. RESULTS. Two hours of occlusion therapy increased the nonamblyopic eye predominance over the amblyopic eye compared with pretreatment measurements, consistent with the results in adults. The boost of the nonamblyopic eye was still present after 1 month of treatment, steadily decreasing afterward to reach pretreatment levels after 2 months of continuous occlusion. Across subjects, the increase in nonamblyopic eye predominance observed after 2 hours of occlusion correlated (rho =-0.65, P =0.04) with the visual acuity improvement of the amblyopic eye measured after 2 months of treatment. CONCLUSIONS. Homeostatic plasticity operates during occlusion therapy for moderate amblyopia and the increase in nonamblyopic eye dominance observed at the beginning of treatment correlates with the amblyopic eye recovery rate. These results suggest that binocular rivalry might be used to monitor visual cortical plasticity during occlusion therapy, although further investigations on larger clinical populations are needed to validate the predictive power of the technique

Perceptual oscillations in gender classification of faces, contingent on stimulus history

Perception is a proactive ‘‘predictive’’ process, in which the brain takes advantage of past experience to make informed guesses about the world to test against sensory data. Here we demonstrate that in the judgment of the gender of faces, beta rhythms play an important role in communicating perceptual experience. Observers classified in forced choice as male or female, a sequence of face stimuli, which were physically constructed to be male or female or androgynous (equal morph). Classification of the androgynous stimuli oscillated rhythmically between male and female, following a complex waveform comprising 13.5 and 17 Hz. Parsing the trials based on the preceding stimulus showed that responses to androgynous stimuli preceded by male stimuli oscillated reliably at 17 Hz, whereas those preceded by female stimuli oscillated at 13.5 Hz. These results suggest that perceptual priors for face perception from recent perceptual memory are communicated through frequency-coded beta rhythms

"Non-retinotopic processing" in Ternus motion displays modeled by spatiotemporal filters

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Quantum spin models for numerosity perception

Humans share with animals, both vertebrates and invertebrates, the capacity to sense the number of items in their environment already at birth. The pervasiveness of this skill across the animal kingdom suggests that it should emerge in very simple populations of neurons. Current modelling literature, however, has struggled to suggest a simple architecture carrying out this task, with most proposals suggesting the emergence of number sense in multi-layered complex neural networks, and typically requiring supervised learning. We present a simple quantum spin model with all-to-all connectivity, where numerosity is encoded in the spectrum after stimulation with a number of transient signals occurring in a random or orderly temporal sequence. We use a paradigmatic simulational approach borrowed from the theory and methods of open quantum systems out of equilibrium, as a possible way to describe information processing in neural systems. Our method is able to capture many of the perceptual characteristics of numerosity in such systems. The frequency components of the magnetization spectra at harmonics of the system's tunneling frequency increase with the number of stimuli presented. The amplitude decoding of each spectrum, performed with an ideal-observer model, reveals that the system follows Weber's law, one of the hallmarks of numerosity perception across the animal kingdom. This contrasts with the well-known failure to reproduce Weber's law with linear system or accumulators models.Comment: 19 pages, 9 figure

Cortical thickness of primary visual cortex correlates with motion deficits in periventricular leukomalacia

Abstract Impairments of visual motion perception and, in particular, of flow motion have been consistently observed in premature and very low birth weight subjects during infancy. Flow motion information is analyzed at various cortical levels along the dorsal pathways, with information mainly provided by primary and early visual cortex (V1, V2 and V3). We investigated the cortical stage of the visual processing that underlies these motion impairments, measuring Grey Matter Volume and Cortical Thickness in 13 children with Periventricular Leukomalacia (PVL). The cortical thickness, but not the grey matter volume of area V1, correlates negatively with motion coherence sensitivity, indicating that the thinner the cortex, the better the performance among the patients. However, we did not find any such association with either the thickness or volume of area MT, MST and areas of the IPS, suggesting damage at the level of primary visual cortex or along the optic radiation