Spatiotemporal frequency and speed tuning in the owl visual wulst

The avian visual wulst is hodologically equivalent to the mammalian primary visual cortex (V1). In contrast to most birds, owls have a massive visual wulst, which shares striking functional similarities with V1. To provide a better understanding of how motion is processed within this area, we used sinusoidal gratings to characterize the spatiotemporal frequency and speed tuning profiles of 131 neurones recorded from awake burrowing owls. Cells were found to be clearly tuned to both spatial and temporal frequencies, and in a way that is similar to what has been reported in the striate cortex of primates and carnivores. Our results also suggest the presence of spatial frequency tuning domains in the wulst. Speed tuning was assessed by several methods devised to measure the degree of dependence between spatial and temporal frequency tuning. Although many neurones were found to be independently tuned, a significant proportion of cells showed at least some degree of dependence, compatible with the idea that some kind of initial transformation towards an explicit representation of speed is being carried out by the owl wulst. Interestingly, under certain constraints, a higher incidence of spatial frequency-invariant speed tuned profiles was obtained by combining our experimentally measured responses using a recent cortical model of speed tuning. Overall, our findings reinforce the notion that, like V1, the owl wulst is an important initial stage for motion processing, a function that is usually attributed to areas of the tectofugal pathway in lateral-eyed birds.     

Pattern motion is present in V1 of awake but not anaesthetized monkeys

We compared responses of neurons, recorded in striate cortex (area V1) of awake, fixating monkeys, to a single drifting grating with those to a 'plaid' pattern comprised of two superimposed drifting gratings separated in orientation by 90 degrees. Five out of 54 (9%) of V1 direction selective neurons responded to the direction of motion of the whole pattern [pattern motion (PM) selectivity]. Tuning curves for plaid stimuli were similar in both optimum direction and width of tuning to those for single gratings. Twenty nine out of 54 (54%) responded simply to the motion of individual orientated gratings within the pattern [component motion (CM) selectivity]. The remaining 37% (20/54) neurons were unclassified. In control experiments, 39 direction selective neurons were recorded in area V1 of anaesthetized monkey and cats. Unlike area V1 in behaving monkeys, none of these neurons exhibited PM selectivity to the drifting plaids. Twenty eight out of 39 (72%) of them responded to the direction of the component gratings and were classified as CM selectivity. Our results indicate that although most V1 neurons are CM selective, as described in anaesthetized animals, a subpopulation is clearly PM selective in behaving monkeys, reflecting integration of locally derived motion signals. Neurons in V1 therefore carry signals that may contribute to pattern motion processing and perception. This perceptual interpretation in V1 might depend much more critically on information integration mechanisms that only function properly in awake, perceiving animals.     

Dynamics of macaque MT cell responses to grating triplets

Neurons in area MT are sensitive to the direction of motion of gratings and of plaids made by summing 2 gratings moving in different directions. MT component direction-selective (CDS) neurons respond to the individual gratings of a plaid. Pattern direction-selective (PDS) neurons on the other hand, combine component information and respond selectively to the resulting pattern motion. Adding a third grating creates a "triplaid," which contains 3 grating and 3 plaid motions and is perceptually multistable. To examine how direction-selective mechanisms parse the motion signals in triplaids, we recorded MT responses of anesthetized and awake macaques to stimuli in which 3 identical moving gratings whose directions were separated by 120° were introduced in 3 successive epochs, going from grating to plaid to triplaid. CDS and PDS neurons-selected based on their responses to gratings and plaids-had strikingly different tuning properties in the triplaid epoch. CDS neurons were strongly tuned for the direction of motion of individual gratings, but PDS neurons nearly lost their selectivity for either the gratings or the plaids in the stimulus. We explain this reduced motion selectivity with a model that relates pattern selectivity of PDS neurons to a broad pooling of V1 afferents with a near-cosine weighting profile. Because PDS neurons signal both component and pattern motion in gratings and plaids, their reduced selectivity for motion in triplaids may be what makes these stimuli perceptually multistable.     

Receptive field properties of single cells in the pigeon's optic tectum during cooling of the ‘visual wulst’

In birds, efferents from the visual telencephalon (visual wulst) terminate in the ipsilateral and contralateral optic tectum. This study concerns the influence of a bilateral cryogenic block of the wulst on the receptive field properties of the visual tectal cells in the pigeon. Tectal units were tested for their responses to static and moving stimuli before, during and after cooling the wulst. For some units the cryogenic block of the wulst was repeated twice. The responsiveness to static and moving stimuli was decreased in most of the tectal cells when the neural activity of the wulst was blocked. In contrast, in some units cooling the wulst provokes an increase of responsiveness. These results indicate that the wulst-tectum path is able to convey both excitatory and inhibitory influences.Other receptive field properties such as the spatial location of the light and dark excitatory regions in the field, the effect of the surround, the size and shape of the excitatory region, the relative responsiveness to static and moving stimuli and the ‘spontaneous activity’ were not affected by wulst cooling.Directional tuning curves were obtained in 18 directionally selective cells before, during and after wulst cooling. In 6 of them the cryogenic block provoked a reduction in directional selectivity either by way of a reduction of the preferred response (4 cells) or by way of an increase of the non-preferred responses (2 cells). In two others directionally selective cells, cooling the wulst provoked a total loss of directional selectivity due to a reduction of the response to the preferred direction together with an increase of the response to the null direction. These results show: (1) that the retinal directional selective input to the tectum is affected by the cryogenic block of the wulst; and (2) that the visual wulst provokes a sharpening of the directional tuning at the optic tectum level.     

Role of primary visual cortex in the binocular integration of plaid motion perception

This study assessed the early mechanisms underlying perception of plaid motion. Thus, two superimposed gratings drifting in a rightward direction composed plaid stimuli whose global motion direction was perceived as the vector sum of the two components. The first experiment was aimed at comparing the perception of plaid motion when both components were presented to both eyes (dioptic) or separately to each eye (dichoptic). When components of the patterns had identical spatial frequencies, coherent motion was correctly perceived under dioptic and dichoptic viewing condition. However, the perceived direction deviated from the predicted direction when spatial frequency differences were introduced between components in both conditions. The results suggest that motion integration follows similar rules for dioptic and dichoptic plaids even though performance under dichoptic viewing did not reach dioptic levels. In the second experiment, the role of early cortical areas in the processing of both plaids was examined. As convergence of monocular inputs is needed for dichoptic perception, we tested the hypothesis that primary visual cortex (V1) is required for dichoptic plaid processing by delivering repetitive transcranial magnetic stimulation to this area. Ten minutes of magnetic stimulation disrupted subsequent dichoptic perception for approximately 15 min, whereas no significant changes were observed for dioptic plaid perception. Taken together, these findings suggest that V1 is not crucial for the processing of dioptic plaids but it is necessary for the binocular integration underlying dichoptic plaid motion perception.     

Pattern motion selectivity in population responses of area 18

It is commonly believed that the complexity of visual stimuli represented by individual neurons increases towards higher cortical areas. However, even in early visual areas an individual neuron's response is influenced by stimuli presented outside its classical receptive field. Thus, it has been proven difficult to characterize the coding of complex stimuli at the level of single neurons. We therefore investigated population responses using optical imaging in cat area 18 to complex stimuli, plaids. Plaid stimuli are composed of two superimposed gratings moving in different directions. They may be perceived as either two separate surfaces or as a global pattern moving in intermediate direction to the components' direction of motion. We found that in addition to activity maps representing the individual components' motion, plaid stimuli produced activity distributions matching the predictions from a pattern-motion model in central area 18. Thereby, relative component- and pattern-like modulations followed the degree of psychophysical pattern bias in the stimulus. Thus, our results strongly indicate that area 18 exhibits a substantial response to pattern-motion signals at the population level suggesting the presence of intrinsic or extrinsic mechanisms that allow for integration of motion responses from far outside the classical receptive field.     

A double dissociation between striate and extrastriate visual cortex for pattern motion perception revealed using rTMS

The neural mechanisms underlying the integration and segregation of motion signals are often studied using plaid stimuli. These stimuli consist of two spatially coincident dynamic gratings of differing orientations, which are either perceived to move in two unique directions or are integrated by the visual system to elicit the percept of a checkerboard moving in a single direction. Computations pertaining to the motion of the individual component gratings are thought to take place in striate cortex (V1) whereas motion integration is thought to involve neurons in dorsal stream extrastriate visual areas, particularly V5/MT. By combining a psychophysical task that employed plaid stimuli with 1 Hz offline repetitive transcranial magnetic stimulation (rTMS), we demonstrated a double dissociation between striate and extrastriate visual cortex in terms of their contributions to motion integration. rTMS over striate cortex increased coherent motion percepts whereas rTMS over extrastriate cortex had the opposite effect. These effects were robust directly after the stimulation administration and gradually returned to baseline within 15 minutes. This double dissociation is consistent with previous patient data and the recent hypothesis that both coherent and transparent motion percepts are supported by the visual system simultaneously and compete for perceptual dominance. Hum Brain Mapp 2009. © 2009 Wiley‐Liss, Inc.     

Bimodal optomotor response to plaids in blowflies: mechanisms of component selectivity and evidence for pattern selectivity

Many animals estimate their self-motion and the movement of external objects by exploiting panoramic patterns of visual motion. To probe how visual systems process compound motion patterns, superimposed visual gratings moving in different directions, plaid stimuli, have been successfully used in vertebrates. Surprisingly, nothing is known about how visually guided insects process plaids. Here, we explored in the blowfly how the well characterized yaw optomotor reflex and the activity of identified visual interneurons depend on plaid stimuli. We show that contrary to previous expectations, the yaw optomotor reflex shows a bimodal directional tuning for certain plaid stimuli. To understand the neural correlates of this behavior, we recorded the responses of a visual interneuron supporting the reflex, the H1 cell, which was also bimodally tuned to the plaid direction. Using a computational model, we identified the essential neural processing steps required to capture the observed response properties. These processing steps have functional parallels with mechanisms found in the primate visual system, despite different biophysical implementations. By characterizing other visual neurons supporting visually guided behaviors, we found responses that ranged from being bimodally tuned to the stimulus direction (component-selective), to responses that appear to be tuned to the direction of the global pattern (pattern-selective). Our results extend the current understanding of neural mechanisms of motion processing in insects, and indicate that the fly employs a wider range of behavioral responses to multiple motion cues than previously reported.     

Pattern and motion vision in cats with selective loss of cortical directional selectivity

Neurons in the visual cortex of cats reared in 8 Hz stroboscopic illumination show a profound loss of directional selectivity, but no detectable deficits in orientation selectivity, contrast sensitivity, and temporal frequency response, and only a slight reduction in spatial resolution. In the present study, spatial vision, temporal resolution, and a variety of motion detection and discrimination thresholds were examined behaviorally in such cats. These psychophysical measurements revealed nearly normal spatial and temporal vision, but severe abnormalities in visual discriminations based on differences in stimulus direction. Specifically, strobe-reared cats showed normal orientation discrimination and temporal frequency resolution, nearly normal contrast sensitivity at low spatial frequencies, and a slight reduction of sensitivity to high spatial frequencies. At high contrasts, the cats were able to discriminate opposite directions of motion over a wide range of visible speeds, and their performance was indistinguishable from that of normal cats. However, a comparison of contrast thresholds for detecting moving gratings and for discriminating their direction of motion revealed severe abnormalities in strobe-reared animals. At low spatial frequencies (0.28 cycles/deg), normal cats could discriminate the direction of grating motion at contrasts that were just barely visible, whereas the strobe-reared cats could detect the grating at contrasts similar to those required by normal cats, but required contrasts about 10 X the threshold to identify the direction of motion. Normal cats showed nearly identical contrast sensitivity for detecting and discriminating gratings of high spatial frequency at high temporal frequency (drift rates), but when the temporal frequency was low, their sensitivity for detection exceeded that for direction discrimination.(ABSTRACT TRUNCATED AT 250 WORDS)     

Spatial and temporal selectivity in the suprasylvian visual cortex of the cat

We recorded from single units in the medial and lateral banks of the posterolateral suprasylvian visual cortex (PMLS/PLLS) of the cat. The responses to drifting high-contrast gratings of optimum orientation and direction of motion, but varying in spatial and temporal frequency, were examined quantitatively for a sample of cells, whose receptive fields covered a wide range of eccentricities. The optimum spatial frequencies (average about 0.2 cycles/deg) were low compared to the values reported for striate cortex but similar to those for area 18. The mean spatial bandwidth (about 2 octaves) was slightly broader than that of cells in other cortical visual areas. The cut-off spatial frequencies ("acuities") covered a wide range, from 0.05 to 2.1 cycles/deg, similar to those of cells in area 18. Responses to drifting sinusoidal gratings were usually dominated by an unmodulated elevation of discharge, although some modulation occurred at the temporal frequency of drift, especially at low spatial frequencies. Modulated responses were relatively stronger in PMLS than in PLLS. For those cells that responded to flashed stimuli, stationary, contrast-modulated gratings presented at different spatial positions typically evoked small responses at the fundamental frequency (dependent on spatial phase) and a larger component at the second harmonic of temporal frequency, with no overall "null-position." The optimum spatial frequency was usually higher than would be predicted by simple summation within the dimensions of the receptive field. Thus, neurons in PMLS and PLLS, like complex cells in areas 17 and 18, behave nonlinearly and their spatial selectivity is determined by "subunits" smaller than their receptive fields. The range of preferred temporal frequencies ranged from less than 2.5 Hz to more than 10 Hz. In their temporal selectivity neurons in PMLS resembled cells in area 17, with little attenuation at low temporal frequencies, whereas there was a tendency for cells in PLLS to prefer higher temporal frequencies, as is common in area 18.     

Centrifugal organization of direction preferences in the cat's lateral suprasylvian visual cortex and its relation to flow field processing

The cerebral cortex of the cat contains between 1 and 2 dozen representations of the visual field with different functional specializations. Six visual field maps lie along both banks of the suprasylvian sulcus, lateral and anterior to the visual areas in the occipital cortex. We have studied single-unit receptive field properties and their global organization across the visual field in 2 of these lateral suprasylvian areas, PMLS (essentially the Clare-Bishop area) and PLLS. Most neurons in PMLS and PLLS display selectivity for the direction of a light stimulus moving across their receptive fields with various degrees of directional tuning. We have used light spots of different size and velocity projected on a tangent screen in order to determine the direction preference of cells in these 2 areas. A strong tendency was found for neurons to respond best to centrifugal directions, i.e., to movement away from the area centralis. Thus, for these cells direction preference depends on the location of their receptive fields within the visual field. Velocity preference and binocular interaction in these neurons is also globally organized: Velocity preference increases with eccentricity, binocular synergism is strongest in the center of the visual field. Cluster analysis of recording tracks with respect to "radial" and "circular" cell categories reveals a grouping of cells with like properties in the lateral suprasylvian cortex. These new categories are formed by combining "centrifugal" and "centripetal" cells on the one hand and cells with direction preferences orthogonal to these on the other. The radial or centrifugal organization of direction preferences in conjunction with the global arrangement of velocity preference and binocular interaction suggests that PMLS and PLLS are involved in the processing of expanding visual flow fields of motion. Such flow fields are commonly encountered when a visual object moves towards an observer or during forward locomotion.     

Parvocellular pathway impairment in autism spectrum disorder: Evidence from visual evoked potentials

In humans, visual information is processed via parallel channels: the parvocellular (P) pathway analyzes color and form information, whereas the magnocellular (M) stream plays an important role in motion analysis. Individuals with autism spectrum disorder (ASD) often show superior performance in processing fine detail, but impaired performance in processing global structure and motion information. To date, no visual evoked potential (VEP) studies have examined the neural basis of atypical visual performance in ASD. VEPs were recorded using 128-channel high density EEG to investigate whether the P and M pathways are functionally altered in ASD. The functioning of the P and M pathways within primary visual cortex (V1) were evaluated using chromatic (equiluminant red–green sinusoidal gratings) and achromatic (low contrast black–white sinusoidal gratings) stimuli, respectively. Unexpectedly, the N1 component of VEPs to chromatic gratings was significantly prolonged in ASD patients compared to controls. However, VEP responses to achromatic gratings did not differ significantly between the two groups. Because chromatic stimuli preferentially stimulate the P-color but not the P-form pathway, our findings suggest that ASD is associated with impaired P-color pathway activity. Our study provides the first electrophysiological evidence for P-color pathway impairments with preserved M function at the V1 level in ASD.     

Auditory motion does not modulate spiking activity in the middle temporal and medial superior temporal visual areas

The integration of multiple sensory modalities is a key aspect of brain function, allowing animals to take advantage of concurrent sources of information to make more accurate perceptual judgments. For many years, multisensory integration in the cerebral cortex was deemed to occur only in high‐level “polysensory” association areas. However, more recent studies have suggested that cross‐modal stimulation can also influence neural activity in areas traditionally considered to be unimodal. In particular, several human neuroimaging studies have reported that extrastriate areas involved in visual motion perception are also activated by auditory motion, and may integrate audiovisual motion cues. However, the exact nature and extent of the effects of auditory motion on the visual cortex have not been studied at the single neuron level. We recorded the spiking activity of neurons in the middle temporal (MT) and medial superior temporal (MST) areas of anesthetized marmoset monkeys upon presentation of unimodal stimuli (moving auditory or visual patterns), as well as bimodal stimuli (concurrent audiovisual motion). Despite robust, direction selective responses to visual motion, none of the sampled neurons responded to auditory motion stimuli. Moreover, concurrent moving auditory stimuli had no significant effect on the ability of single MT and MST neurons, or populations of simultaneously recorded neurons, to discriminate the direction of motion of visual stimuli (moving random dot patterns with varying levels of motion noise). Our findings do not support the hypothesis that direct interactions between MT, MST and areas low in the hierarchy of auditory areas underlie audiovisual motion integration.     

Dynamics of population response to changes of motion direction in primary visual cortex

The visual system is thought to represent the direction of moving objects in the relative activity of large populations of cortical neurons that are broadly tuned to the direction of stimulus motion, but how changes in the direction of a moving stimulus are represented in the population response remains poorly understood. Here we take advantage of the orderly mapping of direction selectivity in ferret primary visual cortex (V1) to explore how abrupt changes in the direction of a moving stimulus are encoded in population activity using voltage-sensitive dye imaging. For stimuli moving in a constant direction, the peak of the V1 population response accurately represented the direction of stimulus motion, but following abrupt changes in motion direction, the peak transiently departed from the direction of stimulus motion in a fashion that varied with the direction offset angle and was well predicted from the response to the component directions. We conclude that cortical dynamics and population coding mechanisms combine to place constraints on the accuracy with which abrupt changes in direction of motion can be represented by cortical circuits.     

Auditory and visual neurons in the cat''s superior colliculus selective for the direction of apparent motion stimuli

In the cat, cells of the superior colliculus (SC) and the tectofugal pathways of the visual system are highly selective for the direction of a moving visual stimulus. Deep layer units of SC in addition respond to auditory and somatosensory stimuli, but the proportion of such non-visual cells is usually found to be much lower than that of visual cells. We recorded the responses of 174 cells in the SC to sequentially presented, localized visual and/or auditory stimuli that produced the sensation of apparent motion to human observers. Controls using single LED flashes or tone pips or clicks at very long intervals that did not produce apparent motion were also used. We found both visual and auditory units that responded vigorously to the apparent motion stimuli and showed pronounced directional selectivity. However, in the auditory domain such units were rare and thus did not increase the proportion of auditory responses in SC substantially. Varying the interstimulus interval (ISI) of these stimuli, both visual and auditory, indicated that the mechanism of direction selectivity in these cells was suppression of the response in the 'non-preferred' direction rather than facilitation in the 'preferred' direction. With long ISI's of 200 ms or more, every single stimulus gave a discrete response peak of constant amplitude. For ISI's of 50 ms or less the discrete peaks merged to a continuous response. Maximal firing rate in the preferred direction remained the same as for longer ISI's, but was decreased for movement in the non-preferred directions. Very short ISI's (10 ms) produced little response in any direction.(ABSTRACT TRUNCATED AT 250 WORDS)     

Encoding of global visual motion in the nidopallium caudolaterale of behaving crows

Songbirds possess acute vision. How higher brain centres represent basic and parameterised visual stimuli to process sensory signals according to their behavioural importance has not been studied in a systematic way. We therefore examined how carrion crows (Corvus corone) and their nidopallial visual neurons process global visual motion information in dynamic random‐dot displays during a delayed match‐to‐sample (DMS) task. The behavioural data show that moderately fast motion speeds (16° of visual angle/s) result in superior direction discrimination performance. To characterise how neurons encode and maintain task‐relevant visual motion information, we recorded the single‐unit activity in the telencephalic association area ‘nidopallium caudolaterale’ (NCL) of behaving crows. The NCL is considered to be the avian analogue of the mammalian prefrontal cortex. Almost a third (28%) of randomly selected NCL neurons responded selectively to the motion direction of the sample stimulus, mostly to downward motions. Only few NCL neurons (7.5%) responded consistently to specific motion directions during the delay period. In error trials, when the crows chose the wrong motion direction, the encoding of motion direction was significantly reduced. This indicates that sensory representations of NCL neurons are relevant to the birds’ behaviour. These data suggest that the corvid NCL, even though operating at the apex of the telencephalic processing hierarchy, constitutes a telencephalic site for global motion integration.     

Functional influence of areas 17, 18, and 19 on lateral suprasylvian cortex in kittens and adult cats: implications for compensation following early visual cortex damage

The aim of the present study was to investigate the mechanisms of physiological compensation that is seen in the posteromedial lateral suprasylvian (PMLS) cortex of cats that received visual cortex (areas 17, 18, and 19) damage early in life. The strategy was to compare the response properties of PMLS neurons just after visual cortex damage (before any compensation has occurred) with the properties of PMLS neurons in normal cats and cats with long-standing visual cortex damage. Fourteen animals (aged 8 weeks, 18 weeks, 26 weeks, or adult) received a unilateral visual cortex lesion and recordings were made from ipsilateral PMLS cortex within about 24 h. An additional 4 adult cats were studied within either 24 or 3 h of a bilateral visual cortex lesion. Results from these animals were compared with results from normal cats and cats with long-standing visual cortex damage studied previously in this laboratory. At all ages studied, an acute visual cortex lesion reduced the percentage of direction-sensitive cells in PMLS cortex from nearly 80% in normal cats to about 20% after the lesion. In 8- and 18-week-old kittens, nearly all of the remaining PMLS cells responded best to stimulus movement but were not direction sensitive. In 26-week-old and adult cats, the remaining cells were divided between those that responded to movement without a directional preference and those that responded as well to stationary flashed stimuli as to moving stimuli. The presence of receptive-field surround inhibition was not affected significantly by an acute lesion at any age. In addition, few PMLS cells were orientation selective to elongated slits of light in cats with an acute lesion, just as in normal cats. The ocular dominance distributions of PMLS neurons also were normal following an acute visual cortex lesion at all ages studied. These results suggest that the influences of areas 17, 18, and 19 on the response properties of PMLS neurons are the same when the properties first reach maturity as in adult cats. The results also suggest that the mechanisms of physiological compensation for an early visual cortex lesion differ for different response properties. Compensation of direction sensitivity and orientation selectivity (an anomalous property) develops de novo after the early lesion. In contrast, compensation of ocular dominance appears to be due to the maintenance of a preexisting property that is present immediately after the lesion. Thus, plasticity after early visual cortex damage represents multiple developmental changes in the remaining visual pathways.     

Local visual energy mechanisms revealed by detection of global patterns

A central goal of visual neuroscience is to relate the selectivity of individual neurons to perceptual judgments, such as detection of a visual pattern at low contrast or in noise. Since neurons in early areas of visual cortex carry information only about a local patch of the image, detection of global patterns must entail spatial pooling over many such neurons. Physiological methods provide access to local detection mechanisms at the single-neuron level but do not reveal how neural responses are combined to determine the perceptual decision. Behavioral methods provide access to perceptual judgments of a global stimulus but typically do not reveal the selectivity of the individual neurons underlying detection. Here we show how the existence of a nonlinearity in spatial pooling does allow properties of these early mechanisms to be estimated from behavioral responses to global stimuli. As an example, we consider detection of large-field sinusoidal gratings in noise. Based on human behavioral data, we estimate the length and width tuning of the local detection mechanisms and show that it is roughly consistent with the tuning of individual neurons in primary visual cortex of primate. We also show that a local energy model of pooling based on these estimated receptive fields is much more predictive of human judgments than competing models, such as probability summation. In addition to revealing underlying properties of early detection and spatial integration mechanisms in human cortex, our findings open a window on new methods for relating system-level perceptual judgments to neuron-level processing.     

The dual nature of the BOLD signal: Responses in visual area hMT+ reflect both input properties and perceptual decision

Neuroimaging studies have suggested that hMT+ encodes global motion interpretation, but this contradicts the notion that BOLD activity mainly reflects neuronal input. While measuring fMRI responses at 7 Tesla, we used an ambiguous moving stimulus, yielding the perception of two incoherently moving surfaces—component motion—or only one coherently moving surface—pattern motion, to induce perceptual fluctuations and identify perceptual organization size‐matched domains in hMT+. Then, moving gratings, exactly matching either the direction of component or pattern motion percepts of the ambiguous stimulus, were shown to the participants to investigate whether response properties reflect the input or decision. If hMT+ responses reflect the input, component motion domains (selective to incoherent percept) should show grating direction stimulus‐dependent changes, unlike pattern motion domains (selective to the coherent percept). This hypothesis is based on the known direction‐selective nature of inputs in component motion perceptual domains versus non‐selectivity in pattern motion perceptual domains. The response amplitude of pattern motion domains did not change with grating direction (consistently with their non‐selective input), in contrast to what happened for the component motion domains (consistently with their selective input). However, when we analyzed relative ratio measures they mirrored perceptual interpretation. These findings are consistent with the notion that patterns of BOLD responses reflect both sensory input and perceptual read‐out.     

Laminar analysis of motion information processing in macaque V5

Although it has been repeatedly shown that properties of striate cells depend on laminar position, no information is available about the vertical organization of primate extrastriate cortex. Laminar analysis in the part of macaque V5 (the middle temporal visual area) devoted to the central 10 degrees in the visual field, reveals that interaction between a moving bar and a moving texture differs systematically between layers. We found that cells for which the direction selectivity does not depend on texture motion occur mainly in layer 4 and in the infragranular layers. Cells with only pseudomodulation of direction selectivity were found throughout the cortical depth. Cells for which direction selectivity was abolished when both patterns moved inphase occur outside layer 4 and therefore represent a higher processing stage. These 3 types differ not only in laminar position but also in velocity selectivity and in strength of texture response. These findings suggest that the 3 classes represent distinct physiological types of neurons dedicated to different stages of motion processing which takes place in V5, and suggest that these cells may play different roles in the guidance of eye movements.