Browsing by Subject "Saccades"
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Item Open Access A pathway in primate brain for internal monitoring of movements.(Science, 2002-05-24) Sommer, Marc A; Wurtz, Robert HIt is essential to keep track of the movements we make, and one way to do that is to monitor correlates, or corollary discharges, of neuronal movement commands. We hypothesized that a previously identified pathway from brainstem to frontal cortex might carry corollary discharge signals. We found that neuronal activity in this pathway encodes upcoming eye movements and that inactivating the pathway impairs sequential eye movements consistent with loss of corollary discharge without affecting single eye movements. These results identify a pathway in the brain of the primate Macaca mulatta that conveys corollary discharge signals.Item Open Access Auditory signals evolve from hybrid- to eye-centered coordinates in the primate superior colliculus.(Journal of neurophysiology, 2012-07) Lee, Jungah; Groh, Jennifer MVisual and auditory spatial signals initially arise in different reference frames. It has been postulated that auditory signals are translated from a head-centered to an eye-centered frame of reference compatible with the visual spatial maps, but, to date, only various forms of hybrid reference frames for sound have been identified. Here, we show that the auditory representation of space in the superior colliculus involves a hybrid reference frame immediately after the sound onset but evolves to become predominantly eye centered, and more similar to the visual representation, by the time of a saccade to that sound. Specifically, during the first 500 ms after the sound onset, auditory response patterns (N = 103) were usually neither head nor eye centered: 64% of neurons showed such a hybrid pattern, whereas 29% were more eye centered and 8% were more head centered. This differed from the pattern observed for visual targets (N = 156): 86% were eye centered, <1% were head centered, and only 13% exhibited a hybrid of both reference frames. For auditory-evoked activity observed within 20 ms of the saccade (N = 154), the proportion of eye-centered response patterns increased to 69%, whereas the hybrid and head-centered response patterns dropped to 30% and <1%, respectively. This pattern approached, although did not quite reach, that observed for saccade-related activity for visual targets: 89% were eye centered, 11% were hybrid, and <1% were head centered (N = 162). The plainly eye-centered visual response patterns and predominantly eye-centered auditory motor response patterns lie in marked contrast to our previous study of the intraparietal cortex, where both visual and auditory sensory and motor-related activity used a predominantly hybrid reference frame (Mullette-Gillman et al. 2005, 2009). Our present findings indicate that auditory signals are ultimately translated into a reference frame roughly similar to that used for vision, but suggest that such signals might emerge only in motor areas responsible for directing gaze to visual and auditory stimuli.Item Open Access Bottom-up and Top-down Mechanisms of Visually-Guided Movements(2016) Rao, Hrishikesh MohanInteracting with the world is a two-step process of accurate sensing followed by coordinated movement. Optimization of biologically-inspired robotic systems benefits from the quantification and modeling of natural sensorimotor behavior, including the bottom-up circuits that mediate it and top-down cognitive influences that modulate it. A critical sensorimotor behavior in everyday life is the generation of rapid eye movements, called saccades. By making saccades 2-3 times/second, we scan visual scenes and integrate the incoming visual signals to construct an internal representation of what is around us. Much is still unknown about the neural processes that act on visual input and the nature of the resulting internal construct. To study this, we first created a model with architecture inspired by known visuomotor circuits in the brain. By training the model to achieve visuomotor stability while varying its visual and motor inputs, we found that it converged onto a solution that resembled and explained a dynamic neural process that had been documented electrophysiologically. Second, in a psychophysical experiment, we kept constant the visual stimuli and motor actions but manipulated the expectations of what subjects thought would happen. We found that visual perception systematically changes based on expectation, providing evidence for cognitive influences on visuomotor integration and continuity. Third, we expanded the work to whole-body orienting in an immersive virtual environment. While performing a marksmanship task, subjects learned to precisely intercept moving targets. Analysis and modeling of the dynamics of movement revealed mechanisms of learning in this realistic behavioral context. Taken together, the studies provide a link between the ensemble activity of neurons and perceptual experience, demonstrate that perception is a combination of incoming signals and prior beliefs, and move the field toward the study of perception-action cycles during natural human behavior.
Item Open Access Brain circuits for the internal monitoring of movements.(Annu Rev Neurosci, 2008) Sommer, Marc A; Wurtz, Robert HEach movement we make activates our own sensory receptors, thus causing a problem for the brain: the spurious, movement-related sensations must be discriminated from the sensory inputs that really matter, those representing our environment. Here we consider circuits for solving this problem in the primate brain. Such circuits convey a copy of each motor command, known as a corollary discharge (CD), to brain regions that use sensory input. In the visual system, CD signals may help to produce a stable visual percept from the jumpy images resulting from our rapid eye movements. A candidate pathway for providing CD for vision ascends from the superior colliculus to the frontal cortex in the primate brain. This circuit conveys warning signals about impending eye movements that are used for planning subsequent movements and analyzing the visual world. Identifying this circuit has provided a model for studying CD in other primate sensory systems and may lead to a better understanding of motor and mental disorders.Item Open Access Compensatory saccades made to remembered targets following orbital displacement by electrically stimulating the dorsomedial frontal cortex or frontal eye fields of primates.(Brain Res, 1996-07-15) Tehovnik, EJ; Sommer, MAIf the eye-position signal during visually-evoked saccades is dependent on the dorsomedial frontal cortex (DMFC), one would expect that saccades generated to briefly presented visual targets would be disrupted after displacement of the eyes via electrical stimulation of this cortical area. Compared are compensatory saccades evoked to brief targets following stimulation of the DMFC and frontal eye fields (FEF). Compensatory saccades produced to brief targets following perturbation via the DMFC were not affected. Accordingly, electrical stimulation of the DMFC does not disrupt the eye-position signal during the execution of visually-evoked saccades.Item Open Access Composition and topographic organization of signals sent from the frontal eye field to the superior colliculus.(J Neurophysiol, 2000-04) Sommer, MA; Wurtz, RHThe frontal eye field (FEF) and superior colliculus (SC) contribute to saccadic eye movement generation, and much of the FEF's oculomotor influence may be mediated through the SC. The present study examined the composition and topographic organization of signals flowing from FEF to SC by recording from FEF neurons that were antidromically activated from rostral or caudal SC. The first and most general result was that, in a sample of 88 corticotectal neurons, the types of signals relayed from FEF to SC were highly diverse, reflecting the general population of signals within FEF rather than any specific subset of signals. Second, many neurons projecting from FEF to SC carried signals thought to reflect cognitive operations, namely tonic discharges during the delay period of a delayed-saccade task (delay signals), elevated discharges during the gap period of a gap task (gap increase signals), or both. Third, FEF neurons discharging during fixation were found to project to the SC, although they did not project preferentially to rostral SC, where similar fixation neurons are found. Neurons that did project preferentially to the rostral SC were those with foveal visual responses and those pausing during the gap period of the gap task. Many of the latter neurons also had foveal visual responses, presaccadic pauses in activity, and postsaccadic increases in activity. These two types of rostral-projecting neurons therefore may contribute to the activity of rostral SC fixation neurons. Fourth, conduction velocity was used as an indicator of cell size to correct for sampling bias. The outcome of this correction procedure suggested that among the most prevalent neurons in the FEF corticotectal population are those carrying putative cognitive-related signals, i.e., delay and gap increase signals, and among the least prevalent are those carrying presaccadic burst discharges but lacking peripheral visual responses. Fifth, corticotectal neurons carrying various signals were biased topographically across the FEF. Neurons with peripheral visual responses but lacking presaccadic burst discharges were biased laterally, neurons with presaccadic burst discharges but lacking peripheral visual responses were biased medially, and neurons carrying delay or gap increase signals were biased dorsally. Finally, corticotectal neurons were distributed within the FEF as a function of their visual or movement field eccentricity and projected to the SC such that eccentricity maps in both structures were closely aligned. We conclude that the FEF most likely influences the activity of SC neurons continuously from the start of fixation, through visual analysis and cognitive manipulations, until a saccade is generated and fixation begins anew. Furthermore, the projection from FEF to SC is highly topographically organized in terms of function at both its source and its termination.Item Open Access Contributions of Bayesian and Discriminative Models to Active Visual Perception across Saccades(2022) Subramanian, DivyaThe brain must interpret sensory inputs to guide movement and behavior, but movements themselves disrupt sensory inputs. Maintaining perceptual continuity through these disruptions requires one to resolve whether sensory inputs were externally generated or caused by one’s own movements. Understanding the sensory world while moving through it constitutes active perception. Saccadic eye movements in primates are a good model system for studying active perception. Eye movements displace the image sensed by the eye, yet the visual system can distinguish movement-induced displacement from external object displacement. How does the brain resolve this uncertainty?
One way is to directly discriminate between sensory states and map them onto percepts in a bottom-up manner. Alternatively, the system could develop an internal model of the world it could use to generate predictions for its sensory inputs. If the input is then ambiguous, the system can default to its predictions more for perception. Bayes rule formalizes how internally generated predictions may compensate for sensory uncertainty. The goal of this dissertation is to investigate the relative contributions of Discriminative and Bayesian processes to active visual perception across saccades.
We performed a series of psychophysical, computational, and neural recording experiments grounded in variations of a task known as “saccadic suppression of displacement,” in which subjects report whether a visual object moved while they made a saccade. First, we found that when humans provided continuous estimates of where an object landed across a saccade, they used a Bayesian model. That is, they used internally generated predictions, or priors, to compensate for sensory uncertainty. However, when asked to provide a categorical report (“did the object move? Yes or no?”) in the same task, they were Anti-Bayesian. They used their priors less with increasing uncertainty. Further investigation in another primate species, rhesus macaques, showed that in the categorical task, priors were used more to compensate for motor-induced uncertainty generated by the saccade. When visual noise was added to the viewed object, however, prior use was Anti-Bayesian, consistent with results from human participants. Decreasing prior use was explained by a Discriminative, neural network model instead. In the macaques, we then recorded single neuron activity during the categorical tasks in a brain region known to signal object displacement across saccades, the Frontal Eye Field (FEF). We compared FEF activity to Bayesian and Discriminative behavior in the motor- and image-noise tasks, respectively. The results showed a clear distinction: the activity of FEF neurons predicted Discriminative but not Bayesian behavior.
In summary, we show that the selection of Bayesian vs. Discriminative models depends on both task requirements and the source of uncertainty. Further, a neural pathway which includes FEF selectively predicts behavior consistent with the use of Discriminative model, implying that the Bayesian model is implemented in a different circuit. These results demonstrate a dissociation between Bayesian and Discriminative models at the computational and neural levels and set the stage for understanding how they interact for perception across saccades.
Item Open Access Delay activity of saccade-related neurons in the caudal dentate nucleus of the macaque cerebellum.(J Neurophysiol, 2013-04) Ashmore, Robin C; Sommer, Marc AThe caudal dentate nucleus (DN) in lateral cerebellum is connected with two visual/oculomotor areas of the cerebrum: the frontal eye field and lateral intraparietal cortex. Many neurons in frontal eye field and lateral intraparietal cortex produce "delay activity" between stimulus and response that correlates with processes such as motor planning. Our hypothesis was that caudal DN neurons would have prominent delay activity as well. From lesion studies, we predicted that this activity would be related to self-timing, i.e., the triggering of saccades based on the internal monitoring of time. We recorded from neurons in the caudal DN of monkeys (Macaca mulatta) that made delayed saccades with or without a self-timing requirement. Most (84%) of the caudal DN neurons had delay activity. These neurons conveyed at least three types of information. First, their activity was often correlated, trial by trial, with saccade initiation. Correlations were found more frequently in a task that required self-timing of saccades (53% of neurons) than in a task that did not (27% of neurons). Second, the delay activity was often tuned for saccade direction (in 65% of neurons). This tuning emerged continuously during a trial. Third, the time course of delay activity associated with self-timed saccades differed significantly from that associated with visually guided saccades (in 71% of neurons). A minority of neurons had sensory-related activity. None had presaccadic bursts, in contrast to DN neurons recorded more rostrally. We conclude that caudal DN neurons convey saccade-related delay activity that may contribute to the motor preparation of when and where to move.Item Open Access Division of labor in frontal eye field neurons during presaccadic remapping of visual receptive fields.(J Neurophysiol, 2012-10) Shin, Sooyoon; Sommer, Marc AOur percept of visual stability across saccadic eye movements may be mediated by presaccadic remapping. Just before a saccade, neurons that remap become visually responsive at a future field (FF), which anticipates the saccade vector. Hence, the neurons use corollary discharge of saccades. Many of the neurons also decrease their response at the receptive field (RF). Presaccadic remapping occurs in several brain areas including the frontal eye field (FEF), which receives corollary discharge of saccades in its layer IV from a collicular-thalamic pathway. We studied, at two levels, the microcircuitry of remapping in the FEF. At the laminar level, we compared remapping between layers IV and V. At the cellular level, we compared remapping between different neuron types of layer IV. In the FEF in four monkeys (Macaca mulatta), we identified 27 layer IV neurons with orthodromic stimulation and 57 layer V neurons with antidromic stimulation from the superior colliculus. With the use of established criteria, we classified the layer IV neurons as putative excitatory (n = 11), putative inhibitory (n = 12), or ambiguous (n = 4). We found that just before a saccade, putative excitatory neurons increased their visual response at the RF, putative inhibitory neurons showed no change, and ambiguous neurons increased their visual response at the FF. None of the neurons showed presaccadic visual changes at both RF and FF. In contrast, neurons in layer V showed full remapping (at both the RF and FF). Our data suggest that elemental signals for remapping are distributed across neuron types in early cortical processing and combined in later stages of cortical microcircuitry.Item Open Access Electrically evoked saccades from the dorsomedial frontal cortex and frontal eye fields: a parametric evaluation reveals differences between areas.(Exp Brain Res, 1997-12) Tehovnik, EJ; Sommer, MAUsing electrical stimulation to evoke saccades from the dorsomedial frontal cortex (DMFC) and frontal eye fields (FEF) of rhesus monkeys, parametric tests were conducted to compare the excitability properties of these regions. Pulse frequency and pulse current, pulse frequency and train duration, and pulse current and pulse duration were varied to determine threshold functions for a 50% probability of evoking a saccade. Also a wide range of frequencies were tested to evoke saccades, while holding all other parameters constant. For frequencies beyond 150 Hz, the probability of evoking saccades decreased for the DMFC, whereas for the FEF this probability remained at 100%. To evoke saccades readily from the DMFC, train durations of greater than 200 ms were needed; for the FEF, durations of less than 100 ms were sufficient. Even though the chronaxies of neurons residing in the DMFC and FEF were similar (ranging from 0.1 to 0.24 ms) significantly higher currents were required to evoke saccades from the DMFC than FEF. Thus the stimulation parameters that are optimal for evoking saccades from the DMFC differ from those that are optimal for evoking saccades from the FEF. Although the excitability of neurons in the DMFC and FEF are similar (due to similar chronaxies), we suggest that the density of saccade-relevant neurons is higher in the FEF than in the DMFC.Item Open Access Express averaging saccades in monkeys.(Vision Res, 1999) Chou, IH; Sommer, MA; Schiller, PHWhen monkeys are presented simultaneously with multiple stimuli, they can make one of two types of response. Either they make averaging saccades, that land at intermediate locations between the targets, or target-directed saccades, that land close to one of the targets. The two types of saccades occur at different latencies and are thought to reflect different processes; fast reflexive averaging and slower target selection. We investigated the latency of averaging saccades in five monkeys, with particular emphasis on 'express' latency saccades, which are thought to be inhibited by target selection. Express averaging saccades were made prolifically by the two monkeys that made both express and regular latency saccades, but only when no specific instruction was given regarding the saccade target. When these monkeys had to choose one of the targets, on the basis of its color, they still made averaging saccades. However, the endpoints formed two distributions close to the targets as opposed to one single distribution centered between the targets, as was the case when targets were identical; also, express saccades were almost entirely absent. We conclude that express averaging saccades are a form of spatial and temporal optimization of gaze shifting.Item Open Access Express saccades elicited during visual scan in the monkey.(Vision Res, 1994-08) Sommer, MAMonkeys trained to saccade to visual targets can develop separate "express" and "regular" modes in their distribution of saccadic latencies. The purpose of this study was to determine whether this occurs under more natural viewing conditions, when targets are suddenly presented in a structured visual field during visual scan. It was found that scanning saccades stopped appearing 60 msec after a target's onset, and subsequent saccades, which were directed toward the suddenly appearing target, had a bimodal distribution of latencies. Express saccades were more likely to occur as the target was presented later in a fixation. Regular mode saccades were more likely to occur with longer target durations. Scanning saccades made to stimuli of the structured visual field always had unimodal inter-saccadic interval distributions. All these effects were apparent after only 2-3 days of training. These findings, taken together with recent physiological results, suggest that the visuomotor cells of the superior colliculus mediate latency bimodality.Item Open Access Feature-specific clusters of neurons and decision-related neuronal activity.(The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014-06) Mayo, J Patrick; Verhoef, Bram-ErnstItem Open Access Frontal eye field neurons assess visual stability across saccades.(J Neurosci, 2012-02-22) Crapse, Trinity B; Sommer, Marc AThe image on the retina may move because the eyes move, or because something in the visual scene moves. The brain is not fooled by this ambiguity. Even as we make saccades, we are able to detect whether visual objects remain stable or move. Here we test whether this ability to assess visual stability across saccades is present at the single-neuron level in the frontal eye field (FEF), an area that receives both visual input and information about imminent saccades. Our hypothesis was that neurons in the FEF report whether a visual stimulus remains stable or moves as a saccade is made. Monkeys made saccades in the presence of a visual stimulus outside of the receptive field. In some trials, the stimulus remained stable, but in other trials, it moved during the saccade. In every trial, the stimulus occupied the center of the receptive field after the saccade, thus evoking a reafferent visual response. We found that many FEF neurons signaled, in the strength and timing of their reafferent response, whether the stimulus had remained stable or moved. Reafferent responses were tuned for the amount of stimulus translation, and, in accordance with human psychophysics, tuning was better (more prevalent, stronger, and quicker) for stimuli that moved perpendicular, rather than parallel, to the saccade. Tuning was sometimes present as well for nonspatial transaccadic changes (in color, size, or both). Our results indicate that FEF neurons evaluate visual stability during saccades and may be general purpose detectors of transaccadic visual change.Item Open Access Frontal eye field neurons orthodromically activated from the superior colliculus.(J Neurophysiol, 1998-12) Sommer, MA; Wurtz, RHFrontal eye field neurons orthodromically activated from the superior colliculus. J. Neurophysiol. 80: 3331-3333, 1998. Anatomical studies have shown that the frontal eye field (FEF) and superior colliculus (SC) of monkeys are reciprocally connected, and a physiological study described the signals sent from the FEF to the SC. Nothing is known, however, about the signals sent from the SC to the FEF. We physiologically identified and characterized FEF neurons that are likely to receive input from the SC. Fifty-two FEF neurons were found that were orthodromically activated by electrical stimulation of the intermediate or deeper layers of the SC. All the neurons that we tested (n = 34) discharged in response to visual stimulation. One-half also discharged when saccadic eye movements were made. This provides the first direct evidence that the ascending pathway from SC to FEF might carry visual- and saccade-related signals. Our findings support a hypothesis that the SC and the FEF interact bidirectionally during the events leading up to saccade generation.Item Open Access Frontal eye field sends delay activity related to movement, memory, and vision to the superior colliculus.(J Neurophysiol, 2001-04) Sommer, MA; Wurtz, RHMany neurons within prefrontal cortex exhibit a tonic discharge between visual stimulation and motor response. This delay activity may contribute to movement, memory, and vision. We studied delay activity sent from the frontal eye field (FEF) in prefrontal cortex to the superior colliculus (SC). We evaluated whether this efferent delay activity was related to movement, memory, or vision, to establish its possible functions. Using antidromic stimulation, we identified 66 FEF neurons projecting to the SC and we recorded from them while monkeys performed a Go/Nogo task. Early in every trial, a monkey was instructed as to whether it would have to make a saccade (Go) or not (Nogo) to a target location, which permitted identification of delay activity related to movement. In half of the trials (memory trials), the target disappeared, which permitted identification of delay activity related to memory. In the remaining trials (visual trials), the target remained visible, which permitted identification of delay activity related to vision. We found that 77% (51/66) of the FEF output neurons had delay activity. In 53% (27/51) of these neurons, delay activity was modulated by Go/Nogo instructions. The modulation preceded saccades made into only part of the visual field, indicating that the modulation was movement-related. In some neurons, delay activity was modulated by Go/Nogo instructions in both memory and visual trials and seemed to represent where to move in general. In other neurons, delay activity was modulated by Go/Nogo instructions only in memory trials, which suggested that it was a correlate of working memory, or only in visual trials, which suggested that it was a correlate of visual attention. In 47% (24/51) of FEF output neurons, delay activity was unaffected by Go/Nogo instructions, which indicated that the activity was related to the visual stimulus. In some of these neurons, delay activity occurred in both memory and visual trials and seemed to represent a coordinate in visual space. In others, delay activity occurred only in memory trials and seemed to represent transient visual memory. In the remainder, delay activity occurred only in visual trials and seemed to be a tonic visual response. In conclusion, the FEF sends diverse delay activity signals related to movement, memory, and vision to the SC, where the signals may be used for saccade generation. Downstream transmission of various delay activity signals may be an important, general way in which the prefrontal cortex contributes to the control of movement.Item Open Access Looking at the ventriloquist: visual outcome of eye movements calibrates sound localization.(PloS one, 2013-01) Pages, Daniel S; Groh, Jennifer MA general problem in learning is how the brain determines what lesson to learn (and what lessons not to learn). For example, sound localization is a behavior that is partially learned with the aid of vision. This process requires correctly matching a visual location to that of a sound. This is an intrinsically circular problem when sound location is itself uncertain and the visual scene is rife with possible visual matches. Here, we develop a simple paradigm using visual guidance of sound localization to gain insight into how the brain confronts this type of circularity. We tested two competing hypotheses. 1: The brain guides sound location learning based on the synchrony or simultaneity of auditory-visual stimuli, potentially involving a Hebbian associative mechanism. 2: The brain uses a 'guess and check' heuristic in which visual feedback that is obtained after an eye movement to a sound alters future performance, perhaps by recruiting the brain's reward-related circuitry. We assessed the effects of exposure to visual stimuli spatially mismatched from sounds on performance of an interleaved auditory-only saccade task. We found that when humans and monkeys were provided the visual stimulus asynchronously with the sound but as feedback to an auditory-guided saccade, they shifted their subsequent auditory-only performance toward the direction of the visual cue by 1.3-1.7 degrees, or 22-28% of the original 6 degree visual-auditory mismatch. In contrast when the visual stimulus was presented synchronously with the sound but extinguished too quickly to provide this feedback, there was little change in subsequent auditory-only performance. Our results suggest that the outcome of our own actions is vital to localizing sounds correctly. Contrary to previous expectations, visual calibration of auditory space does not appear to require visual-auditory associations based on synchrony/simultaneity.Item Open Access Metacognition in monkeys during an oculomotor task.(J Exp Psychol Learn Mem Cogn, 2011-03) Middlebrooks, Paul G; Sommer, Marc AThis study investigated whether rhesus monkeys show evidence of metacognition in a reduced, visual oculomotor task that is particularly suitable for use in fMRI and electrophysiology. The 2-stage task involved punctate visual stimulation and saccadic eye movement responses. In each trial, monkeys made a decision and then made a bet. To earn maximum reward, they had to monitor their decision and use that information to bet advantageously. Two monkeys learned to base their bets on their decisions within a few weeks. We implemented an operational definition of metacognitive behavior that relied on trial-by-trial analyses and signal detection theory. Both monkeys exhibited metacognition according to these quantitative criteria. Neither external visual cues nor potential reaction time cues explained the betting behavior; the animals seemed to rely exclusively on internal traces of their decisions. We documented the learning process of one monkey. During a 10-session transition phase, betting switched from random to a decision-based strategy. The results reinforce previous findings of metacognitive ability in monkeys and may facilitate the neurophysiological investigation of metacognitive functions.Item Open Access Multielectrode evidence for spreading activity across the superior colliculus movement map.(J Neurophysiol, 2000-07) Port, NL; Sommer, MA; Wurtz, RHThe monkey superior colliculus (SC) has maps for both visual input and movement output in the superficial and intermediate layers, respectively, and activity on these maps is generally related to visual stimuli only in one part of the visual field and/or to a restricted range of saccadic eye movements to those stimuli. For some neurons within these maps, however, activity has been reported to spread from the caudal SC to the rostral SC during the course of a saccade. This spread of activity was inferred from averages of recordings at different sites on the SC movement map during saccades of different amplitudes and even in different monkeys. In the present experiments, SC activity was recorded simultaneously in pairs of neurons to observe the spread of activity during individual saccades. Two electrodes were positioned along the rostral-caudal axis of the SC with one being more caudal than the other, and 60 neuron pairs whose movement fields were large enough to see a spread of activity were studied. During individual saccades, the relative time of discharge of the two neurons was compared using 1) the time difference between peak discharge of the two neurons, 2) the difference between the "median activation time" of the two neurons, and 3) the shift required to align the two discharge patterns using cross-correlation. All three analysis methods gave comparable results. Many pairs of neurons were activated in sequence during saccade generation, and the order of activation was most frequently caudal to rostral. Such a sequence of activation was not observed in every neuron pair, but over the sample of neuron pairs studied, the spread was statistically significant. When we compared the time of neuronal activity to the time of saccade onset, we found that the caudal neuronal activity was more likely to be before the saccade, whereas the rostral neuronal activity was more likely to be during the saccade. These results demonstrate that when individual pairs of neurons are examined during single saccades there is evidence of a caudal to rostral spread of activity within the monkey SC, and they confirm the previous inferences of a spread of activity drawn from observations on averaged neuronal activity during multiple saccades. The functional contribution of this spread of activity remains to be determined.Item Open Access Neuronal adaptation caused by sequential visual stimulation in the frontal eye field.(J Neurophysiol, 2008-10) Mayo, J Patrick; Sommer, Marc AImages on the retina can change drastically in only a few milliseconds. A robust description of visual temporal processing is therefore necessary to understand visual analysis in the real world. To this end, we studied subsecond visual changes and asked how prefrontal neurons in monkeys respond to stimuli presented in quick succession. We recorded the visual responses of single neurons in the frontal eye field (FEF), a prefrontal area polysynaptically removed from the retina that is involved with higher level cognition. For comparison, we also recorded from small groups of neurons in the superficial superior colliculus (supSC), an area that receives direct retinal input. Two sequential flashes of light at varying interstimulus intervals were presented in a neuron's receptive field. We found pervasive neuronal adaptation in FEF and supSC. Visual responses to the second stimulus were diminished for up to half a second after the first stimulus presentation. Adaptation required a similar amount of time to return to full responsiveness in both structures, but there was significantly more neuronal adaptation overall in FEF. Adaptation was not affected by saccades, although visual responses to single stimuli were transiently suppressed postsaccadically. Our FEF and supSC results systematically document subsecond visual adaptation in prefrontal cortex and show that this adaptation is comparable to, but stronger than, adaptation found earlier in the visual system.