Trans-saccadic

Humans actively sample their environment with saccadic eye movements to bring relevant information into high-acuity foveal vision. Despite being lower in resolution, peripheral information is also available before each saccade. How the pre-saccadic extrafoveal preview of a visual object influences its post-saccadic processing is still an unanswered question. The current study investigated this question by simultaneously recording behavior and fixation-related brain potentials while human subjects made saccades to face stimuli...

Values are attributed to goods during free viewing of objects which entails multi- and trans-saccadic cognitive processes. Using electroencephalographic eye-fixation related potentials, the present study investigated how neural signals related to value-guided choice evolved over time when viewing household and office products during an auction task. Participants completed a Becker-DeGroot-Marschak auction task whereby half of the stimuli were presented in either a free or forced bid protocol to obtain willingness-to-pay...

INTRODUCTION: Spatial remapping, the process of updating information across eye movements, is an important mechanism for trans-saccadic perception. The right posterior parietal cortex (PPC) is a region that has been associated most strongly with spatial remapping. The aim of the project was to investigate the effect of damage to the right PPC on direction specific trans-saccadic memory. We compared trans-saccadic memory performance for central items that had to be remembered while making a left- versus rightward eye movement, or for items that were remapped within the left versus right visual field...

The world appears stable despite saccadic eye-movements. One possible explanation for this phenomenon is that the visual system predicts upcoming input across saccadic eye-movements based on peripheral preview of the saccadic target. We tested this idea using concurrent electroencephalography (EEG) and eye-tracking. Participants made cued saccades to peripheral upright or inverted face stimuli that changed orientation (invalid preview) or maintained orientation (valid preview) while the saccade was completed...

Current models of trans-saccadic perception propose that, after a saccade, the saccade target object must be localized among objects near the landing position. However, the nature of the attentional mechanisms supporting this process is currently under debate. In the present study, we tested whether surface properties of the saccade target object automatically bias post-saccadic selection using a variant of the visual search task. Participants executed a saccade to a shape-singleton target in a circular array...

Even though we frequently execute saccades, we perceive the external world as coherent and stable. An important mechanism of trans-saccadic perception is spatial remapping: the process of updating information across eye movements. Previous studies have indicated a right hemispheric dominance for spatial remapping, which has been proposed to translate into enhanced trans-saccadic memory for locations that are remapped into the right compared to the left hemisphere in healthy participants. Previous study designs suffered from several limitations, however (i...

By predicting sensory consequences of actions, humans can distinguish self-generated sensory inputs from those that are elicited externally. This is one mechanism by which we achieve a subjective sense of agency over our actions. Corollary discharge signals (CD)-"copies" of motor signals sent to sensory areas-permit such predictions, and CD abnormalities are a hypothesized mechanism for the agency disruptions in schizophrenia that characterize a subset of symptoms. Indeed, behavioral evidence of altered CD, including in the oculomotor system, has been observed in schizophrenia patients...

Saccadic eye movements alter the visual processing of objects of interest by bringing them from the periphery, where there is only low-resolution vision, to the high-resolution fovea. Evidence suggests that people are able to achieve trans-saccadic integration in a near-optimal manner; however the mechanisms underlying integration are still unclear. Visual working memory (VWM) is sustained across a saccade, and it has been suggested that this memory resource is used to store and compare the pre- and post- saccadic percepts...

Recent studies using the gaze-contingent boundary paradigm reported a reversed preview benefit -shorter fixations on a target word when an unrelated preview was easier to process than the fixated target (Schotter & Leinenger, 2016). This is explained via forced fixations -short fixations on words that would ideally be skipped (because lexical processing has progressed enough) but could not be because saccade planning reached a point of no return. This contrasts with accounts of preview effects via trans-saccadic integration -shorter fixations on a target word when the preview is more similar to it (see Cutter, Drieghe, & Liversedge, 2015)...

Maintaining a continuous, stable perception of the visual world relies on the ability to integrate information from previous fixations with the current one. An essential component of this integration is trans-saccadic memory (TSM), memory for information across saccades. TSM capacity may play a limiting role in tasks requiring efficient trans-saccadic integration, such as multiple-fixation visual search tasks. We estimated TSM capacity and investigated its relationship to visual short-term memory (VSTM) using two visual search tasks, one in which participants maintained fixation while saccades were simulated and another where participants made a sequence of actual saccades...

Does visual processing start anew after each eye movement, or is information integrated across saccades? Here we test a strong prediction of the integration hypothesis: that information acquired after a saccade interferes with the perception of images acquired before the saccade. We investigate perception of a basic visual feature, grating orientation, and we take advantage of a delayed interference phenomenon-in human participants, the reported orientation of a target grating, briefly presented at an eccentric location, is strongly biased toward the orientation of flanker gratings that are flashed shortly after the target...

While making saccadic eye-movements to scan a visual scene, humans and monkeys are able to keep track of relevant visual stimuli by maintaining spatial attention on them. This ability requires a shift of attentional modulation from the neuronal population representing the relevant stimulus pre-saccadically to the one representing it post-saccadically. For optimal performance, this trans-saccadic attention shift should be rapid and saccade-synchronized. Whether this is so is not known. We trained two rhesus monkeys to make saccades while maintaining covert attention at a fixed spatial location...

BACKGROUND: Saccadic eye movements change the retinal location of visual objects, but we do not experience the visual world as constantly moving, we perceive it as seamless and stable. This visual stability may be achieved by an internal or efference copy of each saccade that, combined with the retinal information, allows the visual system to cancel out or ignore the self-caused retinal motion. OBJECTIVE: The current study investigated the underlying brain mechanisms responsible for visual stability in humans with online transcranial magnetic stimulation (TMS)...

With every saccade, humans must reconcile the low resolution peripheral information available before a saccade, with the high resolution foveal information acquired after the saccade. While research has shown that we are able to integrate peripheral and foveal vision in a near-optimal manner, it is still unclear which mechanisms may underpin this important perceptual process. One potential mechanism that may moderate this integration process is visual attention. Pre-saccadic attention is a well documented phenomenon, whereby visual attention shifts to the location of an upcoming saccade before the saccade is executed...

Humans typically make several saccades per second. This provides a challenge for the visual system as locations are largely coded in retinotopic (eye-centered) coordinates. Spatial remapping, the updating of retinotopic location coordinates of items in visuospatial memory, is typically assumed to be limited to robust, capacity-limited and attention-demanding working memory (WM). Are pre-attentive, maskable, sensory memory representations (e.g. fragile memory, FM) also remapped? We directly compared trans-saccadic WM (tWM) and trans-saccadic FM (tFM) in a retro-cue change-detection paradigm...

Saccadic eye movements cause rapid and dramatic displacements of the retinal image of the visual world, yet our conscious perception of the world remains stable and continuous. A popular explanation for this remarkable ability of our visual system to compensate for the displacements is the predictive feature remapping theory. The theory proposes that, before saccades, the representation of a visual stimulus can be predictively transferred from neurons that initially encode the stimulus to neurons whose receptive fields will encompass the stimulus location after the saccade...

When objects move or the eyes move, the visual system can predict the consequence and generate a percept of the target at its new position. This predictive localization may depend on eye movement control in the frontal eye fields (FEF) and the intraparietal sulcus (IPS) and on motion analysis in the medial temporal area (MT). Across two experiments we examined whether repetitive transcranial magnetic stimulation (rTMS) over right FEF, right IPS, right MT, and a control site, peripheral V1/V2, diminished participants' perception of two cases of predictive position perception: trans-saccadic fusion, and the flash grab illusion, both presented in the contralateral visual field...

Only ray-finned fishes possess a torus longitudinalis (TL), a paired, elongated body attached to the medial margins of the optic tectum. Its granule cells project large numbers of fine fibers running laterally over adjacent tectum, synapsing excitatorily on the spiny dendrites of pyramidal cells. Sustained TL activity is evoked visuotopically by dark stimuli; TL bursting is a corollary discharge of saccadic eye movements. To suggest a function for this ancient structure, neural network models were constructed to show that: (1) pyramidal cells could form an attentional locus, selecting one out of several moving objects to track, but rapid image shifts caused by saccades disrupt tracking; (2) TL could supply both the pre-saccade position of a locus, and the shift predicted from a saccade so as to prime pyramidal dendrites at the target location, ensuring the locus stays with the attended object; (3) that the specific pattern of synaptic connections required for such predictive priming could be learned by an unsupervised rule; (4) temporal and spatial filtering of visual pattern input to TL allows learning from a complex scene...

Brain representations of visual space are predominantly eye-centred (retinotopic) yet our experience of the world is largely world-centred (spatiotopic). A long-standing question is how the brain creates continuity between these reference frames across successive eye movements (saccades). Here we use functional magnetic resonance imaging (fMRI) to address whether spatially specific repetition suppression (RS) is evident during trans-saccadic perception. We presented two successive Gabor patches (S1 and S2) in either the upper or lower visual field, left or right of fixation...

The cortical sites for the trans-saccadic storage and integration of visual object features are unknown. Here, we used a variant of fMRI-Adaptation where subjects fixated to the left or right of a briefly presented visual grating, maintained fixation or saccaded to the opposite side, then judged whether a re-presented grating had the same or different orientation. fMRI analysis revealed trans-saccadic interactions (different > same orientation) in a visual field-insensitive cluster within right supramarginal gyrus...