Abstract:Saccadic eye movements cause frequent and substantial displacements of the retinal image, but those displacements go unnoticed. It has been widely assumed that this perceived stability emerges from the shifting of visual receptive fields from their current, presaccadic locations to their future, postsaccadic locations in anticipation of the retinal consequences of saccades. Although evidence consistent with this anticipatory remapping has accumulated over the years, more recent work suggests an alternative vie… Show more
“…Indeed, microsaccades cause perceptual mislocalizations that are believed to be a hallmark of perceptual stability mechanisms [24]. Therefore, attention may be a general component of peri-saccadic perceptual stability [27].…”
Section: Figure 7 a Sustained Influence Of Pre-microsaccadic Sc Modumentioning
confidence: 99%
“…Grating contrast (Lmax À Lmin / Lmax + Lmin) was 5%, 10%, 20%, 40%, or 80%, and phase was randomized. Grating size (filling the RF) was large enough to avoid a potential ''micro'' form of changing/shifting RF's around saccades [27,28]. If such changes occur around microsaccades, they would be small and canceled with large stimuli.…”
Section: Behavioral Tasksmentioning
confidence: 99%
“…It might also be the case that these changes share characteristics with changes observed when attentional allocation is instructed. For example, if microsaccade-related preparatory activity in the superior colliculus (SC) [21] were to provide a ''gain'' modulation signal for visually evoked neuronal activity [24], similar to how it might do with large saccades [25][26][27][28][29][30], then response enhancement could potentially be observed for stimuli appearing before microsaccades, independent of whether a task involved attention. Thus, response enhancement, an attentional signature, can also occur in tight synchrony with individual microsaccades.…”
Neuronal response gain enhancement is a classic signature of the allocation of covert visual attention without eye movements. However, microsaccades continuously occur during gaze fixation. Because these tiny eye movements are preceded by motor preparatory signals well before they are triggered, it may be the case that a corollary of such signals may cause enhancement, even without attentional cueing. In six different macaque monkeys and two different brain areas previously implicated in covert visual attention (superior colliculus and frontal eye fields), we show neuronal response gain enhancement for peripheral stimuli appearing immediately before microsaccades. This enhancement occurs both during simple fixation with behaviorally irrelevant peripheral stimuli and when the stimuli are relevant for the subsequent allocation of covert visual attention. Moreover, this enhancement occurs in both purely visual neurons and visual-motor neurons, and it is replaced by suppression for stimuli appearing immediately after microsaccades. Our results suggest that there may be an obligatory link between microsaccade occurrence and peripheral selective processing, even though microsaccades can be orders of magnitude smaller than the eccentricities of peripheral stimuli. Because microsaccades occur in a repetitive manner during fixation, and because these eye movements reset neurophysiological rhythms every time they occur, our results highlight a possible mechanism through which oculomotor events may aid periodic sampling of the visual environment for the benefit of perception, even when gaze is prevented from overtly shifting. One functional consequence of such periodic sampling could be the magnification of rhythmic fluctuations of peripheral covert visual attention.
“…Indeed, microsaccades cause perceptual mislocalizations that are believed to be a hallmark of perceptual stability mechanisms [24]. Therefore, attention may be a general component of peri-saccadic perceptual stability [27].…”
Section: Figure 7 a Sustained Influence Of Pre-microsaccadic Sc Modumentioning
confidence: 99%
“…Grating contrast (Lmax À Lmin / Lmax + Lmin) was 5%, 10%, 20%, 40%, or 80%, and phase was randomized. Grating size (filling the RF) was large enough to avoid a potential ''micro'' form of changing/shifting RF's around saccades [27,28]. If such changes occur around microsaccades, they would be small and canceled with large stimuli.…”
Section: Behavioral Tasksmentioning
confidence: 99%
“…It might also be the case that these changes share characteristics with changes observed when attentional allocation is instructed. For example, if microsaccade-related preparatory activity in the superior colliculus (SC) [21] were to provide a ''gain'' modulation signal for visually evoked neuronal activity [24], similar to how it might do with large saccades [25][26][27][28][29][30], then response enhancement could potentially be observed for stimuli appearing before microsaccades, independent of whether a task involved attention. Thus, response enhancement, an attentional signature, can also occur in tight synchrony with individual microsaccades.…”
Neuronal response gain enhancement is a classic signature of the allocation of covert visual attention without eye movements. However, microsaccades continuously occur during gaze fixation. Because these tiny eye movements are preceded by motor preparatory signals well before they are triggered, it may be the case that a corollary of such signals may cause enhancement, even without attentional cueing. In six different macaque monkeys and two different brain areas previously implicated in covert visual attention (superior colliculus and frontal eye fields), we show neuronal response gain enhancement for peripheral stimuli appearing immediately before microsaccades. This enhancement occurs both during simple fixation with behaviorally irrelevant peripheral stimuli and when the stimuli are relevant for the subsequent allocation of covert visual attention. Moreover, this enhancement occurs in both purely visual neurons and visual-motor neurons, and it is replaced by suppression for stimuli appearing immediately after microsaccades. Our results suggest that there may be an obligatory link between microsaccade occurrence and peripheral selective processing, even though microsaccades can be orders of magnitude smaller than the eccentricities of peripheral stimuli. Because microsaccades occur in a repetitive manner during fixation, and because these eye movements reset neurophysiological rhythms every time they occur, our results highlight a possible mechanism through which oculomotor events may aid periodic sampling of the visual environment for the benefit of perception, even when gaze is prevented from overtly shifting. One functional consequence of such periodic sampling could be the magnification of rhythmic fluctuations of peripheral covert visual attention.
“…Until about 25 years ago, visual receptive fi elds were thought to be determined entirely by the pattern of retinal inputs, so it was quite surprising to fi nd neurons in primate cortex with receptive fi elds that changed position every time a saccade was executed [1]. Although this discovery has fi gured prominently into theories of visual perception, there is still much debate about the nature of the phenomenon: Some studies report forward remapping Correspondence [1][2][3], in which receptive fi elds shift to their postsaccadic locations, and others report convergent remapping, in which receptive fi elds shift toward the saccade target [4]. These two possibilities can be diffi cult to distinguish, particularly when the two types of remapping lead to receptive fi eld shifts in similar directions [5], as was the case in virtually all previous experiments.…”
mentioning
confidence: 99%
“…An emerging pattern of results shows that the perisaccadic responses of V4 neurons recall the locations of past stimuli [3] and anticipate potential future stimuli [6,10], in addition to their well-known roles in shape recognition and attention. The fact that these different responses are present in the same area, and often in the same neurons, has profound implications for theories of spatial representations in the primate brain [2,4].…”
A fundamental concept in neuroscience is the receptive field, the area of space over which a neuron gathers information. Until about 25 years ago, visual receptive fields were thought to be determined entirely by the pattern of retinal inputs, so it was quite surprising to find neurons in primate cortex with receptive fields that changed position every time a saccade was executed [1]. Although this discovery has figured prominently into theories of visual perception, there is still much debate about the nature of the phenomenon: Some studies report forward remapping[1-3], in which receptive fields shift to their postsaccadic locations, and others report convergent remapping, in which receptive fields shift toward the saccade target [4]. These two possibilities can be difficult to distinguish, particularly when the two types of remapping lead to receptive field shifts in similar directions [5], as was the case in virtually all previous experiments. Here we report new data from neurons in primate cortical area V4, where both types of remapping have previously been reported [3,6]. Using an experimental configuration in which forward and convergent remapping would lead to receptive field shifts in opposite directions, we show that forward remapping is the dominant type of receptive field shift in V4.
IntroductionPathophysiological theories of schizophrenia (SZ) symptoms posit an abnormality in using predictions to guide behavior. One such prediction is based on imminent movements, via corollary discharge signals (CD) that relay information about planned movement kinematics to sensory brain regions. Empirical evidence suggests a reduced influence of sensorimotor predictions in individuals with SZ within multiple sensory systems, including in the visual system. One function of CD in the visual system is to selectively enhance visual sensitivity at the location of planned eye movements (pre‐saccadic attention), thus enabling a prediction of the to‐be‐foveated stimulus. We expected pre‐saccadic attention shifts to be less pronounced in individuals with SZ than in healthy controls (HC), resulting in unexpected sensory consequences of eye movements, which may relate to symptoms than can be explained in the context of altered allocation of attention.MethodsWe examined this question by testing 30 SZ and 30 HC on a pre‐saccadic attention task. On each trial participants made a saccade to a cued location in an array of four stimuli. A discrimination target that was either congruent or incongruent with the cued location was briefly presented after the cue, during saccade preparation. Pre‐saccadic attention was quantified by comparing accuracy on congruent trials to incongruent trials within the interval preceding the saccade.ResultsAlthough SZs were less accurate overall, the magnitude of the pre‐saccadic attention effect generally did not differ across groups nor show a convincing relationship with symptom severity. We did, however, observe that SZ had reduced pre‐saccadic attention effects when the discrimination target (probe) was presented at early stages of saccade planning, when pre‐saccadic attention effects first emerged in HC.ConclusionThese findings suggest generally intact pre‐saccadic shifts of attention in SZ, albeit slightly delayed. Results contribute to our understanding of altered sensory predictions in people with schizophrenia.
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