Eye movements modulate visual receptive fields of V4 neurons

The receptive field, defined as the spatiotemporal selectivity of neurons to sensory stimuli, is central to our understanding of the neuronal mechanisms of perception. However, despite the fact that eye movements are critical during normal vision, the influence of eye movements on the structure of receptive fields has never been characterized. Here, we map the receptive fields of macaque area V4 neurons during saccadic eye movements and find that receptive fields are remarkably dynamic. Specifically, before the initiation of a saccadic eye movement, receptive fields shrink and shift towards the saccade target. These spatiotemporal dynamics may enhance information processing of relevant stimuli during the scanning of a visual scene, thereby assisting the selection of saccade targets and accelerating the analysis of the visual scene during free viewing.     

Reproduction of reaching movements to memorized targets in the lack of visual control

The objective of this study was to examine the precision of reaching movements to remembered target distances in the lack of visual information. Subjects were professional basketball players and nonathlete university students. The basketball players, having well-trained manual skills, performed better than the non-athlete students. Increase in the overestimation of the remembered target distances was found under the effect of fatigue. A weight load on the sliding handle caused some decrease in the errors of reaching the remembered targets. No significant gender differences were found.     

Eye movements and verbal report in a single case of visual neglect

In this single case study, visuospatial neglect patient P1 demonstrated a dissociation between an intact ability to make appropriate reflexive eye movements to targets in the neglected field with latencies of <400 ms, while failing to report targets presented at such durations in a separate verbal detection task. In contrast, there was a failure to evoke the usually robust Remote Distractor Effect in P1, even though distractors in the neglected field were presented at above threshold durations. Together those data indicate that the tight coupling that is normally shown between attention and eye movements appears to be disrupted for low-level orienting in P1. A comparable disruption was also found for high-level cognitive processing tasks, namely reading and scene scanning. The findings are discussed in relation to sampling, attention and awareness in neglect.     

Differences between visually triggered human forearm movements with visual and auditory relevant feedback

The effects of visual and auditory relevant feedback on human forearm movements elicited by random position signal sequences were examined. Forearm movements were performed with four feedback conditions. We observed the reaction time, the holding time, and the adjustment error sequences when the arm moved briskly and accurately to the target position. As the results, the reaction times for auditory relevant feedback were shorter than those for the others (visual or no feedback). The holding times for auditory relevant feedback were longer than those for the others. And the subjects had about one adjustment error to terminate on the target zone.     

Saccadic head movements of the praying mantis, with particular reference to visual and proprioceptive information

ABSTRACT. Horizontal head movements of the praying mantis, Sphodromantis lineola Burm., were recorded continuously. They responded to the presence of a live blowfly prey in the antero-lateral visual field with a rapid saccadic head movement. The angular movement of a fixation saccade was correlated positively to the displacement of the prey from the prothoracic midline. Saccade magnitude and velocity are related. After the stimulus moved out of the visual field, the mantis made a second saccadic head movement, a return saccade towards the body midline. We observed return saccades in which the head overshot or undershot the body midline, as well as saccades which returned the head exactly to its initial position. In 92% of trials with intact mantids, the return movement succeeded eventually in rotating the head back to its initial position, whereas after removal of the neck hair plates this occurred in only 47% of trials. There is a consistent relation between saccade extent and velocity. Velocities of return saccades were slower than those of fixation saccades. It is suggested that sensory inputs from the neck hair plate proprioceptors modify both the magnitude and the angular velocity of fixation and return saccadic head movements.     

Eye movements in heterophoria.

Reference is made to earlier reports by the author in which versional recovery eye movements were observed during the cover test in the non-occluded eye in case of heterophoria. This provided support for Hering's Law, although the magnitude of the versional movement did not relate to the degree of heterophoria. Recent studies of eye movements during the cover test on very small heterophorias have suggested there is a threshold value below which these versional recovery movements are absent, and that is presence depends on such factors as the size of the phoria, the degree of ocular motor dominance and patient concentration.     

Eye movements in Daphnia magna

Summary Three types of behavior of the compound eye of Daphnia magna are characterized: flick, a transient rotation elicited by a brief flash of light; fixation, a maintained eye orientation in response to a stationary light stimulus of long-duration; tracking, the smooth pursuit of a moving stimulus. The magnitudes of the flick and fixation responses vary with stimulus position and are generally proportional to stimulus intensity, although at high intensities there is an attenuation of both behaviors. When the stimulus is placed at a position 80° dorsal to the eye axis, there is no response; this area is called the null region. For stationary stimuli in other positions, the direction of the response is such as to bring the stimulus closer to the null region. During tracking, the relative positions of the eye and stimulus change; the eye velocity is approximately half that of the moving stimulus. The regions of the eye in which these behaviors may be induced are different, being largest for flick and smallest for tracking. It is proposed that flick and fixation responses are a means for rotating the eye so that the stimulus is within the area surrounding the null region which is used for tracking.     

Eye movements predict recollective experience

Previously encountered stimuli can bring to mind a vivid memory of the episodic context in which the stimulus was first experienced ("remembered" stimuli), or can simply seem familiar ("known" stimuli). Past studies suggest that more attentional resources are required to encode stimuli that are subsequently remembered than known. However, it is unclear if the attentional resources are distributed differently during encoding and recognition of remembered and known stimuli. Here, we record eye movements while participants encode photos, and later while indicating whether the photos are remembered, known or new. Eye fixations were more clustered during both encoding and recognition of remembered photos relative to known photos. Thus, recognition of photos that bring to mind a vivid memory for the episodic context in which they were experienced is associated with less distributed overt attention during encoding and recognition. The results suggest that remembering is related to encoding of a few distinct details of a photo rather than the photo as a whole. In turn, during recognition remembering may be trigged by enhanced memory for the salient details of the photos.     

Eye movements and the enhancement of edges

A mathematical examination of retinal photochemistry leads to a hypothesis for Mach band phenomena based on eye movements. This retinal model suggests why minimally distinct borders fade under eye fixation and agrees qualitatively with subjective measures of border contrast as a function of overall field luminance.Deceased     

Eye movements: keeping vision stable

A long-standing problem for vision researchers is how our perception of the world remains stable despite the continual motion of our eyes. Three recent studies begin to shed light on how the visual system suppresses the motion generated by these eye movements.     

Postural adjustments to head movements in the cat

Head movements induced by motor cortex stimulation in the cat are accompanied by variations in the vertical force exerted by each limb. These postural responses were found to show stereotyped patterns: with head dorsiflexions an increase was observed in the force exerted by the anterior limbs and a decrease at the posterior limb level. From comparison between the latencies of the force variations, the beginning of head acceleration, and EMG activity in the limb extensor muscles, it was concluded that triggering of these postural responses is not reflex, but depends on the same command as the movement itself. This early response might be a means of avoiding the downward movement of the trunk which would otherwise result from the reaction force corresponding to the upward head movement.     

Eye movements: building a stable world from glance to glance

Frequent exploratory eye-movements called saccades pose for the visual system the problem of combining information from successive fixations into an apparently seam less conscious experience. A new study shows that information from successive fixations is combined, not by fusing fixation 'snapshots', but by integrating more complex visual attributes at a mid-high level of analysis.     

Eye movements: illusions in slow motion

A recent study has shown that a range of different motion illusions occurring during smooth pursuit eye-movements can be explained as optimal percepts based on a simple model derived from the Bayesian statistical framework.     

Peeping and attachment to visual and auditory stimuli in day-old chicks

The usefulness of peeping in indexing attachment to visual and auditory stimuli was confirmed in chicks between 18 and 30 h post-hatch. Greater attractiveness of the auditory stimulus was associated with a more marked initial reduction in peeping after auditory stimulus presentation, suggesting a greater attentional impact, and with greater effectiveness in reducing peeping during repeated stimulus presentations. There was no difference between the two stimuli in effects on peeping before or shortly after the initial approach to the stimuli. Of additional interest was the observation of a sharp rise in peeping immediately preceding the increased activity associated with initial approach. The possible relationship between peeping and arousal was considered.