Resistance of a short-term memory concealed information test with famous faces to countermeasures.

The concealed information test (CIT) aims at identifying knowledge that a person wants to hide, by measuring physiological indices during the presentation of known versus unknown items. Recently, Lancry-Dayan et al. (Journal of Applied Research in Memory and Cognition, 7 (2), 291-302, 2018) proposed a new version of this test that included a short-term memory task to maximize differences between responses to items.

Empirical validation of QUEST+ in PSE and JND estimations in visual discrimination tasks.

One of the most precise methods to establish psychometric functions and estimate threshold and slope parameters is the constant stimuli procedure. The large distribution of predetermined stimulus values presented to observers enables the psychometric functions to be fully developed, but makes this procedure time-consuming. Adaptive procedures enable reliable threshold estimation while reducing the number of trials by concentrating stimulus presentations around observers' supposed threshold.

Saccadic adaptation shapes perceived size: Common codes for action and perception.

Recent findings suggest that perceptual and motor systems share common codes; for instance, perceived object location is known to correlate with motor changes in the oculomotor system. Here, we investigate whether modifying saccade amplitude affects object size perception. Participants saw in peripheral vision a test disk that could vary in size across trials.

Calibration of peripheral perception of shape with and without saccadic eye movements.

The cortical representations of a visual object differ radically across saccades. Several studies claim that the visual system adapts the peripheral percept to better match the subsequent foveal view. Recently, Herwig, Weiß, and Schneider (2015, Annals of the New York Academy of Sciences, 1339(1), 97-105) found that the perception of shape demonstrates a saccade-dependent learning effect.

Predictive position computations mediated by parietal areas: TMS evidence.

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.

Transsaccadic perceptual fusion.

Transsaccadic perceptual fusion is the integration of pre- and postsaccadic images into a single percept aligned in spatial coordinates. Several early studies reported an absence of transsaccadic fusion between dissimilar patterns, effectively stopping research on this question for three decades. We have now corrected two problematic aspects of these earlier studies and find robust evidence for transsaccadic perceptual fusion.

Visual reinforcement shapes eye movements in visual search.

We use eye movements to gain information about our visual environment; this information can indirectly be used to affect the environment. Whereas eye movements are affected by explicit rewards such as points or money, it is not clear whether the information gained by finding a hidden target has a similar reward value. Here we tested whether finding a visual target can reinforce eye movements in visual search performed in a noise background, which conforms to natural scene statistics and contains a large number of possible target locations.

Reinforcing saccadic amplitude variability in a visual search task.

Human observers often adopt rigid scanning strategies in visual search tasks, even though this may lead to suboptimal performance. Here we ask whether specific levels of saccadic amplitude variability may be induced in a visual search task using reinforcement learning. We designed a new gaze-contingent visual foraging task in which finding a target among distractors was made contingent upon specific saccadic amplitudes.

Reinforcing saccadic amplitude variability.

Saccadic endpoint variability is often viewed as the outcome of neural noise occurring during sensorimotor processing. However, part of this variability might result from operant learning. We tested this hypothesis by reinforcing dispersions of saccadic amplitude distributions, while maintaining constant their medians.

Modification of saccadic gain by reinforcement.

Control of saccadic gain is often viewed as a simple compensatory process in which gain is adjusted over many trials by the postsaccadic retinal error, thereby maintaining saccadic accuracy. Here, we propose that gain might also be changed by a reinforcement process not requiring a visual error. To test this hypothesis, we used experimental paradigms in which retinal error was removed by extinguishing the target at the start of each saccade and either an auditory tone or the vision of the target on the fovea was provided as reinforcement after those saccades that met an amplitude criterion.

Operant control of human eye movements.

Saccade and smooth pursuit are the eye movements used by primates to shift gaze. In this article we review evidence for the effects of reinforcement on several dimensions of these responses such as their latencies, velocities or amplitudes. We propose that these responses are operant behaviours controlled by their consequences on performance of visually guided tasks.