Perceptual learning across saccades: Feature but not location specific.

Perceptual learning is the ability to enhance perception through practice. The hallmark of perceptual learning is its specificity for the trained location and stimulus features, such as orientation. For example, training in discriminating a grating's orientation improves performance only at the trained location but not in other untrained locations.

A dynamic 1/f noise protocol to assess visual attention without biasing perceptual processing.

Psychophysical paradigms measure visual attention via localized test items to which observers must react or whose features have to be discriminated. These items, however, potentially interfere with the intended measurement, as they bias observers' spatial and temporal attention to their location and presentation time. Furthermore, visual sensitivity for conventional test items naturally decreases with retinal eccentricity, which prevents direct comparison of central and peripheral attention assessments.

The effect of spatial structure on presaccadic attention costs and benefits assessed with dynamic 1/f noise.

Already before the onset of a saccadic eye movement, we preferentially process visual information at the upcoming eye fixation. This 'presaccadic shift of attention' is typically assessed via localized test items, which potentially bias the attention measurement. Here we show how presaccadic attention shapes perception from saccade origin to target when no scene-structuring items are presented.

Eye and hand movements disrupt attentional control.

Voluntary attentional control is the ability to selectively focus on a subset of visual information in the presence of other competing stimuli-a marker of cognitive control enabling flexible, goal-driven behavior. To test its robustness, we contrasted attentional control with the most common source of attentional orienting in daily life: attention shifts prior to goal-directed eye and hand movements. In a multi-tasking paradigm, human participants attended at a location while planning eye or hand movements elsewhere.

Sounds are remapped across saccades.

To achieve visual space constancy, our brain remaps eye-centered projections of visual objects across saccades. Here, we measured saccade trajectory curvature following the presentation of visual, auditory, and audiovisual distractors in a double-step saccade task to investigate if this stability mechanism also accounts for localized sounds. We found that saccade trajectories systematically curved away from the position at which either a light or a sound was presented, suggesting that both modalities are represented in eye-centered oculomotor centers.

Attention capture outside the oculomotor range.

Neurophysiological studies have demonstrated that attentional orienting is associated with activity in fronto-parietal brain areas that play a pivotal role in oculomotor control, such as the lateral intraparietal cortex (LIP), the frontal eye fields (FEF), and the superior colliculus (SC) (e.g., [1]).

Stimulus blanking reveals contrast-dependent transsaccadic feature transfer.

Across saccadic eye movements, the visual system receives two successive static images corresponding to the pre- and the postsaccadic projections of the visual field on the retina. The existence of a mechanism integrating the content of these images is today still a matter of debate. Here, we studied the transfer of a visual feature across saccades using a blanking paradigm.

Theory of visual attention (TVA) in action: Assessing premotor attention in simultaneous eye-hand movements.

Attention shifts that precede goal-directed eye and hand movements are regarded as markers of motor target selection. Whether effectors compete for a single, shared attentional resource during simultaneous eye-hand movements or whether attentional resources can be allocated independently towards multiple target locations is controversially debated. Independent, effector-specific target selection mechanisms underlying parallel allocation of visuospatial attention to saccade and reach targets would predict an increase of the overall attention capacity with the number of active effectors.

Visual attention and eye movement control during oculomotor competition.

Saccadic eye movements are typically preceded by selective shifts of visual attention. Recent evidence, however, suggests that oculomotor selection can occur in the absence of attentional selection when saccades erroneously land in between nearby competing objects (saccade averaging). This study combined a saccade task with a visual discrimination task to investigate saccade target selection during episodes of competition between a saccade target and a nearby distractor.

Spatiotopic and saccade-specific transsaccadic memory for object detail.

The content and nature of transsaccadic memory are still a matter of debate. Brief postsaccadic target blanking was demonstrated to recover transsaccadic memory and defeat saccadic suppression of displacement. We examined whether blanking would also support transsaccadic transfer of detailed form information.

Displacement detection is suppressed by the post-saccadic stimulus.

To establish a perceptually stable world despite the large retinal shifts caused by saccadic eye movements, the visual system reduces its sensitivity to the displacement of visual stimuli during saccades (e.g. saccadic suppression of displacement, SSD).

Sensitivity measures of visuospatial attention.

Measuring visual sensitivity has become popular to determine the spatial deployment of visual attention. Critically, the accuracy of the measurement depends on the quality of the stimulus used. We evaluated the strengths and weaknesses of six commonly used stimuli for assessing visual attention.

The spread of presaccadic attention depends on the spatial configuration of the visual scene.

When preparing a saccade, attentional resources are focused at the saccade target and its immediate vicinity. Here we show that this does not hold true when saccades are prepared toward a recently extinguished target. We obtained detailed maps of orientation sensitivity when participants prepared a saccade toward a target that either remained on the screen or disappeared before the eyes moved.

Visual attention is not limited to the oculomotor range.

Both patients with eye movement disorders and healthy participants whose oculomotor range had been experimentally reduced have been reported to show attentional deficits at locations unreachable by their eyes. Whereas previous studies were mainly based on the evaluation of reaction times, we measured visual sensitivity before saccadic eye movements and during fixation at locations either within or beyond participants' oculomotor range. Participants rotated their heads to prevent them from performing large rightward saccades.

Investigating the Deployment of Visual Attention Before Accurate and Averaging Saccades via Eye Tracking and Assessment of Visual Sensitivity.

This experimental protocol was designed to investigate whether visual attention is obligatorily deployed at the endpoint of saccades. To this end, we recorded the eye position of human participants engaged in a saccade task via eye tracking and assessed visual orientation discrimination performance at various locations during saccade preparation. Importantly, instead of using a single saccade target paradigm for which the saccade endpoint typically coincides roughly with the target, this protocol comprised the presentation of two nearby saccade targets, leading to a distinct spatial dissociation between target locations and saccade endpoint on a substantial number of trials.

Saccade selection and inhibition: motor and attentional components.

Motor responses are fundamentally spatial in their function and neural organization. However, studies of inhibitory motor control, focused on global stopping of all actions, have ignored whether inhibitory control can be exercised selectively for specific actions. We used a new approach to elicit and measure motor inhibition by asking human participants to either look at (select) or avoid looking at (inhibit) a location in space.

Pre-saccadic remapping relies on dynamics of spatial attention.

Each saccade shifts the projections of the visual scene on the retina. It has been proposed that the receptive fields of neurons in oculomotor areas are predictively remapped to account for these shifts. While remapping of the whole visual scene seems prohibitively complex, selection by attention may limit these processes to a subset of attended locations.

Independent Effects of Eye and Hand Movements on Visual Working Memory.

Both eye and hand movements have been shown to selectively interfere with visual working memory. We investigated working memory in the context of simultaneous eye-hand movements to approach the question whether the eye and the hand movement systems independently interact with visual working memory. Participants memorized several locations and performed eye, hand, or simultaneous eye-hand movements during the maintenance interval.

The influence of obstacles on grasp planning.

When reaching to grasp for an object in the absence of obstacles, the choice of contact points is highly consistent within and between healthy humans, suggesting a preplanning of grasping movements (Gilster et al. in Exp Brain Res 217:137-151, 2012). In real life, objects may obstruct the favored contact points at a target object, requiring adjustments to avoid collision.

Visual attention is not deployed at the endpoint of averaging saccades.

The premotor theory of attention postulates that spatial attention arises from the activation of saccade areas and that the deployment of attention is the consequence of motor programming. Yet attentional and oculomotor processes have been shown to be dissociable at the neuronal level in covert attention tasks. To investigate a potential dissociation at the behavioral level, we instructed human participants to move their eyes (saccade) towards 1 of 2 nearby, competing saccade targets.

Independent selection of eye and hand targets suggests effector-specific attentional mechanisms.

Both eye and hand movements bind visual attention to their target locations during movement preparation. However, it remains contentious whether eye and hand targets are selected jointly by a single selection system, or individually by independent systems. To unravel the controversy, we investigated the deployment of visual attention - a proxy of motor target selection - in coordinated eye-hand movements.

Pre- and post-saccadic stimulus timing in saccadic suppression of displacement - A computational model.

When the target of a saccadic eye movement is displaced while the eyes move this displacement is often not noticed (saccadic suppression of displacement, SSD). We present a neurobiologically motivated, computational model of SSD and compare its simulation results to experimental data. The model offers a simple explanation of the effects of pre- and post-saccadic stimulus blanking on SSD in terms of peri-saccadic network dynamics.

Spatial attention during saccade decisions.

Behavioral measures of decision making are usually limited to observations of decision outcomes. In the present study, we made use of the fact that oculomotor and sensory selection are closely linked to track oculomotor decision making before oculomotor responses are made. We asked participants to make a saccadic eye movement to one of two memorized target locations and observed that visual sensitivity increased at both the chosen and the nonchosen saccade target locations, with a clear bias toward the chosen target.

Presaccadic motion integration between current and future retinotopic locations of attended objects.

Object tracking across eye movements is thought to rely on presaccadic updating of attention between the object's current and its "remapped" location (i.e., the postsaccadic retinotopic location).

Attention allocation before antisaccades.

In the present study, we investigated the distribution of attention before antisaccades. We used a dual task paradigm, in which participants made prosaccades or antisaccades and discriminated the orientation of a visual probe shown at the saccade goal, the visual cue location (antisaccade condition), or a neutral location. Moreover, participants indicated whether they had made a correct antisaccade or an erroneous prosaccade.