Réponses évoquées par les mouvements oculaires d'exploration (réponse lambda): Rôle des afférences intervenant à divers moments du processus oculo-moteur

Perception ◽  
1972 ◽  
Vol 1 (2) ◽  
pp. 167-175 ◽  
Author(s):  
Nicole Lesèvre ◽  
A Rémond

Experiments are reported the aim of which was to elucidate the cause of each of the components of the lambda response, and particularly to evaluate the role of ‘on’ and ‘off’ visual effects which appear at various times during the oculomotor process and also the possible influence of non-visual mechanisms. Eight subjects with normal sight were studied under the following conditions: (i) horizontal eye movements of 12° were guided by fixation points placed on a dimly-lit uniform black field of 20°; a checkerboard of 6° aperture was placed in this field so as to be integrated into the oculomotor process at different times—at the beginning, during and at the end of the eye movement; (ii) successive horizontal eye movements of 3°, 7° and 11° scanned a checkerboard of 20°, each square of which had a 40′ aperture; (iii) the checkerboard was moved with an amplitude and period similar to those of the eye movements in (ii), but this time with gaze fixed. Horizontal and vertical movements of both eyes were recorded with an EOG. An EEG of the parieto-occipital regions was obtained using eight linked bipolar derivations in line on two montages, median longitudinal and right-left transverse. The EEG and EOG data were digitalized and a numerical programme of waveform recognition was used to identify the beginning of the saccade which triggers the averaging out of the EEG before (100 ms) and after (500 ms) the eye movement. A discussion of the results, taking into account the latency of the different components and their reinforcements or inhibition depending on experimental conditions, suggests that the two initial components of lambda response (including the initial portion of the classical lambda wave) might be due to visual effects (‘off effect’) that arise at the start of the movement or slightly before it at the time that the saccadic suppression begins. The later components could be attributed to visual effects brought into play towards the end of the movement (‘on effect’), when perception becomes normal again. It is, however, difficult to explain some of the results related to the amplitude of lambda components without bringing in a mechanism of non-visual origin (corollary discharge).

2021 ◽  
Author(s):  
◽  
Gary D Bird

<p>Shimojo, Simion, Shimojo and Scheier (2003) provided preliminary evidence that eye movements have an active role in preference formation. In their study, subjects were presented with two faces and chose which was more attractive. By manipulating how long subjects were able to look at each face after an eye movement, Shimojo et al. (2003) showed that faces presented for a longer duration were more likely to be chosen as more attractive. However, a recent study from Nittono and Wada (2009) showed that an eye movement may not be necessary for this effect, as novel graphic patterns presented in the centre of the screen (thus requiring no eye movements) for longer durations were also more likely to be preferred. The purpose of the current study was to further investigate whether eye movements do have an active role in preference formation. The present study used the same paradigm as Shimojo et al.’s (2003) study. Subjects in Experiment 1 were presented with images of two real faces, alternatively (one for 900ms, one for 300ms) for six repetitions. There were 3 independent experimental conditions. One group were required to make eye movements to laterally presented faces and judge attractiveness (lateral attractiveness condition), a second were not required to make eye movements to centrally presented faces and judge attractiveness (central attractiveness condition). The third were required to make eye movements to laterally presented faces and judge roundness (lateral roundness condition). The findings indicated that subjects were more likely to choose the longer presented faces in the lateral attractiveness and central attractiveness conditions, but not the lateral roundness conditions. Experiment 2 was similar to Experiment 1 with the exception of the type of stimuli, which consisted of computer generated faces (CGFs). Subjects were more likely to choose the longer presented CGF in the lateral attractiveness, central attractiveness and lateral roundness conditions. The findings of the present study were not in line with Shimojo et al.’s (2003) previous findings, who found that faces presented for a longer duration were only preferred in the lateral attractiveness condition of their study. It is possible that the faces that are presented for the longer duration in the current paradigm are preferred due to the increase in exposure duration irrespective of an eye movement (as per the findings from Nittono and Wada, 2009). As it is unclear as to whether eye movements play an active role in preference formation, the findings of the present study have not been able to contribute to computational models of decision making.</p>


2021 ◽  
Author(s):  
◽  
Gary D Bird

<p>Shimojo, Simion, Shimojo and Scheier (2003) provided preliminary evidence that eye movements have an active role in preference formation. In their study, subjects were presented with two faces and chose which was more attractive. By manipulating how long subjects were able to look at each face after an eye movement, Shimojo et al. (2003) showed that faces presented for a longer duration were more likely to be chosen as more attractive. However, a recent study from Nittono and Wada (2009) showed that an eye movement may not be necessary for this effect, as novel graphic patterns presented in the centre of the screen (thus requiring no eye movements) for longer durations were also more likely to be preferred. The purpose of the current study was to further investigate whether eye movements do have an active role in preference formation. The present study used the same paradigm as Shimojo et al.’s (2003) study. Subjects in Experiment 1 were presented with images of two real faces, alternatively (one for 900ms, one for 300ms) for six repetitions. There were 3 independent experimental conditions. One group were required to make eye movements to laterally presented faces and judge attractiveness (lateral attractiveness condition), a second were not required to make eye movements to centrally presented faces and judge attractiveness (central attractiveness condition). The third were required to make eye movements to laterally presented faces and judge roundness (lateral roundness condition). The findings indicated that subjects were more likely to choose the longer presented faces in the lateral attractiveness and central attractiveness conditions, but not the lateral roundness conditions. Experiment 2 was similar to Experiment 1 with the exception of the type of stimuli, which consisted of computer generated faces (CGFs). Subjects were more likely to choose the longer presented CGF in the lateral attractiveness, central attractiveness and lateral roundness conditions. The findings of the present study were not in line with Shimojo et al.’s (2003) previous findings, who found that faces presented for a longer duration were only preferred in the lateral attractiveness condition of their study. It is possible that the faces that are presented for the longer duration in the current paradigm are preferred due to the increase in exposure duration irrespective of an eye movement (as per the findings from Nittono and Wada, 2009). As it is unclear as to whether eye movements play an active role in preference formation, the findings of the present study have not been able to contribute to computational models of decision making.</p>


2009 ◽  
Vol 101 (2) ◽  
pp. 934-947 ◽  
Author(s):  
Masafumi Ohki ◽  
Hiromasa Kitazawa ◽  
Takahito Hiramatsu ◽  
Kimitake Kaga ◽  
Taiko Kitamura ◽  
...  

The anatomical connection between the frontal eye field and the cerebellar hemispheric lobule VII (H-VII) suggests a potential role of the hemisphere in voluntary eye movement control. To reveal the involvement of the hemisphere in smooth pursuit and saccade control, we made a unilateral lesion around H-VII and examined its effects in three Macaca fuscata that were trained to pursue visually a small target. To the step (3°)-ramp (5–20°/s) target motion, the monkeys usually showed an initial pursuit eye movement at a latency of 80–140 ms and a small catch-up saccade at 140–220 ms that was followed by a postsaccadic pursuit eye movement that roughly matched the ramp target velocity. After unilateral cerebellar hemispheric lesioning, the initial pursuit eye movements were impaired, and the velocities of the postsaccadic pursuit eye movements decreased. The onsets of 5° visually guided saccades to the stationary target were delayed, and their amplitudes showed a tendency of increased trial-to-trial variability but never became hypo- or hypermetric. Similar tendencies were observed in the onsets and amplitudes of catch-up saccades. The adaptation of open-loop smooth pursuit velocity, tested by a step increase in target velocity for a brief period, was impaired. These lesion effects were recognized in all directions, particularly in the ipsiversive direction. A recovery was observed at 4 wk postlesion for some of these lesion effects. These results suggest that the cerebellar hemispheric region around lobule VII is involved in the control of smooth pursuit and saccadic eye movements.


1995 ◽  
Vol 74 (3) ◽  
pp. 1367-1372 ◽  
Author(s):  
G. Cheron ◽  
S. Saussez ◽  
N. Gerrits ◽  
E. Godaux

1. Properties of nucleus incertus (NIC) neurons projecting to the cerebellar flocculus were studied in alert cats by using chronic unit and eye movement recording and antidromic activation. Projection of these neurons onto the flocculus was verified with retrograde transport of horseradish peroxidase after injections in the flocculus. 2. Bipolar stimulation electrodes were implanted into the "middle" zone of each flocculus because this zone is known to be involved in the control of horizontal eye movements. The dorsomedial aspect of the pontine tegmentum was explored with microelectrodes during stimulation of both flocculi. The majority of neurons antidromically activated from the flocculus were found in the caudal part of the NIC. 3. Of the 69 neurons activated from the flocculus, 44 were classified as burst-tonic (BT) neurons; 34 discharged in relation with horizontal movements of the eye, 10 in relation with vertical movements. Of the 14 remaining neurons, 6 were not related to eye movements and 8 were classified as burst neurons. The BT neurons of the NIC displayed a great sensitivity to both horizontal eye position and horizontal eye velocity. 4. This study demonstrates the presence of a new group of horizontal eye movement related BT neurons situated in the NIC. The fact that they project to the horizontal floccular zone emphasizes the importance of the functional specialization of the different Purkinje cell zones.


1998 ◽  
Vol 80 (4) ◽  
pp. 2046-2062 ◽  
Author(s):  
R. J. Krauzlis ◽  
F. A. Miles

Krauzlis, R. J. and F. A. Miles. Role of the oculomotor vermis in generating pursuit and saccades: effects of microstimulation. J. Neurophysiol. 80: 2046–2062, 1998. We studied the eye movements evoked by applying small amounts of current (2–50 μA) within the oculomotor vermis of two monkeys. We first compared the eye movements evoked by microstimulation applied either during maintained pursuit or during fixation. Smooth, pursuitlike changes in eye velocity caused by the microstimulation were directed toward the ipsilateral side and occurred at short latencies (10–20 ms). The amplitudes of these pursuitlike changes were larger during visually guided pursuit toward the contralateral side than during either fixation or visually guided pursuit toward the ipsilateral side. At these same sites, microstimulation also often produced abrupt, saccadelike changes in eye velocity. In contrast to the smooth changes in eye velocity, these saccadelike effects were more prevalent during fixation and during pursuit toward the ipsilateral side. The amplitude and type of evoked eye movements could also be manipulated at single sites by changing the frequency of microstimulation. Increasing the frequency of microstimulation produced increases in the amplitude of pursuitlike changes, but only up to a certain point. Beyond this point, the value of which depended on the site and whether the monkey was fixating or pursuing, further increases in stimulation frequency produced saccadelike changes of increasing amplitude. To quantify these effects, we introduced a novel method for classifying eye movements as pursuitlike or saccadelike. The results of this analysis showed that the eye movements evoked by microstimulation exhibit a distinct transition point between pursuit and saccadelike effects and that the amplitude of eye movement that corresponds to this transition point depends on the eye movement behavior of the monkey. These results are consistent with accumulating evidence that the oculomotor vermis and its associated deep cerebellar nucleus, the caudal fastigial, are involved in the control of both pursuit and saccadic eye movements. We suggest that the oculomotor vermis might accomplish this role by altering the amplitude of a motor error signal that is common to both saccades and pursuit.


Author(s):  
Jocelyn R. Folk ◽  
Michael A. Eskenazi

This chapter provides an overview of how the observation of eye movement behavior can be used to study how words are identified during reading in different populations. The chapter begins with a discussion of different eye movement behaviors, the perceptual span, and parafoveal processing. After providing the reader with a basic understanding of terms and methodology, the authors discuss how eye movements in reading change across the lifespan, individual differences in eye movement behavior in lower-skill and higher-skill adult readers, and eye movement patterns in special populations. This discussion highlights what is known about changes in eye movement behaviors from developing readers to older adult readers. It also includes a discussion of the role of eye movements in dyslexia and eye movement behavior in readers who are deaf.


2016 ◽  
Vol 10 (1) ◽  
pp. 13-22 ◽  
Author(s):  
Gauranga Jeram Patel ◽  
John McDowall

In dismantling eye movement desensitization and reprocessing (EMDR) therapy, researchers have found that the central executive is likely responsible for the effect of eye movements on negative memories. Arguably, however, researchers have not satisfactorily explained central executive mechanisms responsible. One possible central executive mechanism is that of suppression. The aim of this research was to evaluate the effect of eye movements on vividness, emotionality, and suppression of memories. Thirty-one nonclinical participants in Experiment 1 completed fast- and no-eye-movement conditions. Thirty-three nonclinical participants in Experiment 2 completed fast-, slow-, and no-eye-movement conditions. Number of intrusions during a suppression period and self-ratings of vividness and emotionality were the dependent variables in both experiments. Experiment 2 also included a measure of central executive capacity. Results from both experiments supported the hypotheses and showed that fast eye movements resulted in fewer intrusions than no- and slow-eye-movement conditions. Experiment 2 also found a correlation between number of intrusions after fast eye movements and central executive capacity. Limitations of this research are discussed as well as possibilities for future research and implications for understanding EMDR therapy.


2020 ◽  
Vol 13 (4) ◽  
pp. 72-87
Author(s):  
G.Ya. Menshikova ◽  
A.O. Pichugina

In modern literature, the question of holistic and analytic processing of facial perception and facial expressions is actively debated. Various experimental paradigms have been developed for their study, one of which was based on the face inversion effect. In a number of works to study the role of eye movements in holistic and analytic processing, the procedure of presenting upright and inverted faces was followed by recording eye movements. The results were contradictory: some works revealed significant changes in the characteristics of eye movements in the inversion effect, but the others have not found the changes. The aim of our work was to study individual eye movement strategies in the task of assessing the attractiveness of upright and inverted faces. The participants were 57 students. The results showed that a decrease in the role of holistic processing in the face inversion effect led to a significant change in fixation durations and saccade amplitudes, as well as to a change in the distribution of the dwell time on four areas of interest (eyes, nose, nose bridge and mouth). Two groups of participants with individual types of eye movement strategies (static and dynamic) were identified. Comparing eye movement strategies for upright and inverted faces showed that the dwell time distribution on areas of interest varied significantly depending on the group. These data showed the importance of incorporating the individual eye movement strategies when studying holistic and analytic face processing.


Author(s):  
Maria I. Kiose

The article discusses the role of the age factor in the readers’ comprehension of stylistically heterogeneous texts, here the text fragments containing figurative noun groups of salient and non-salient character. The salience effects on eye movement and default responses are studied in the oculographic experiment where the secondary school children had to read the sentences displaying figurativeness. The earlier detected statistically significant corpus salience indices of referential, linguistic and discourse parameters in figurativeness construal get verified experimentally. In accordance with the Graded Salience and Defaultness hypotheses I assumed that the interpretation of figurative noun groups of varied referential, linguistic and discourse salience will require different cognitive effort in terms of both eye movement reactions and default inferences. Several eye-tracking experiments with adult participants sufficed to prove the dependency, however, the results obtained with children did not support the Salience hypothesis in the part of visual perception. The eye movements of children facing figurative noun groups did not show steady correlation patterns with the salience effects of these groups, whereas the default interpretations correlated strongly with referential, linguistic, and discourse salience. The results show evidence in favor of Mixed-Effects Model of interpretation


2010 ◽  
Vol 104 (4) ◽  
pp. 2187-2193 ◽  
Author(s):  
Angela L. Gee ◽  
Anna E. Ipata ◽  
Michael E. Goldberg

We constantly make eye movements to bring objects of interest onto the fovea for more detailed processing. Activity in area V4, a prestriate visual area, is enhanced at the location corresponding to the target of an eye movement. However, the precise role of activity in V4 in relation to these saccades and the modulation of other cortical areas in the oculomotor system remains unknown. V4 could be a source of visual feature information used to select the eye movement, or alternatively, it could reflect the locus of spatial attention. To test these hypotheses, we trained monkeys on a visual search task in which they were free to move their eyes. We found that activity in area V4 reflected the direction of the upcoming saccade but did not predict the latency of the saccade in contrast to activity in the lateral intraparietal area (LIP). We suggest that the signals in V4, unlike those in LIP, are not directly involved in the generation of the saccade itself but rather are more closely linked to visual perception and attention. Although V4 and LIP have different roles in spatial attention and preparing eye movements, they likely perform complimentary processes during visual search.


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