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Guy A Orban

Publications and source records attributed to Guy A Orban.

At least 19 recordsLinked to original sources

Extracting 3D structure from disparity.

The neural mechanisms of stereoscopic 3D shape perception have only recently been investigated. Here we review the two cortical regions in which these mechanisms have been studied so far in macaques: a small subpart of inferotemporal cortex called TEs, and the caudal intraparietal (CIP) region. Neurons in TEs respond selectively to the orientation and curvature in depth of stereoscopic surfaces and this region provides a detailed 3D shape description of surface boundaries and surface content. This description is evoked only by binocular stimuli in which subjects see depth and it does not vary if depth is specified by different cues. Neurons in CIP are a selective for orientation in depth of surfaces and elongated objects, and their responses are also unaffected by changes in depth cues. Thus, stereoscopic 3D shape is processed in both the dorsal, occipito-parietal and the ventral, occipito-temporal streams.

Animals↗

Learning to see the difference specifically alters the most informative V4 neurons.

Perceptual learning is an instance of adult plasticity whereby training in a sensory (e.g., a visual task) results in neuronal changes leading to an improved ability to perform the task. Yet studies in primary visual cortex have found that changes in neuronal response properties were relatively modest. The present study examines the effects of training in an orientation discrimination task on the response properties of V4 neurons in awake rhesus monkeys. Results indicate that the changes induced in V4 are indeed larger than those in V1. Nonspecific effects of training included a decrease in response variance, and an increase in overall orientation selectivity in V4. The orientation-specific changes involved a local steepening in the orientation tuning curve around the trained orientation that selectively improved orientation discriminability at the trained orientation. Moreover, these changes were largely confined to the population of neurons whose orientation tuning was optimal for signaling small differences in orientation at the trained orientation. Finally, the modifications were restricted to the part of the tuning curve close to the trained orientation. Thus, we conclude that it is the most informative V4 neurons, those most directly involved in the discrimination, that are specifically modified by perceptual learning.

Action Potentials↗

Charting the lower superior temporal region, a new motion-sensitive region in monkey superior temporal sulcus.

Although the role of the middle temporal (MT/V5) area and its medial superior temporal (MST) satellites in motion processing has been well explored, relatively little is known about motion regions located more rostrally in the superior temporal sulcus (STS), such as the fundus of the superior temporal (FST) area, the superior temporal polysensory (STP) region, or beyond. To fill this void, we used contrast-enhanced functional magnetic resonance imaging in awake macaques and a five-step testing procedure that allowed us to identify six motion-sensitive regions within the STS. Direction adaptation tests confirmed the motion sensitivity of these six regions. Five of them [MT/V5, its three satellites, and the middle part of the STP (STPm) region in the upper bank of the STS] have been documented by previous single-cell studies. A sixth, previously unknown motion-responsive region, which we termed the lower superior temporal (LST) region, was observed on the lower bank and fundus of the STS, 6-8 mm anterior to the FST area. In contrast to the MST areas, the LST region responds to slow as well as fast speeds and is responsive to static and moving images of objects, to patterns defined by opponent motion, and to actions. These results, obtained in both group and single-subject analyses, suggest that motion information in the STS might follow a second path, in addition to the MT/V5-MST path. This ventral path including the LST region, FST area, and STPm region is likely involved in the visual analysis of actions and biological motion.

Animals↗

Selectivity of neuronal adaptation does not match response selectivity: a single-cell study of the FMRI adaptation paradigm.

fMRI-based adaptation paradigms (fMR-A) have been used to infer neuronal stimulus selectivities in humans. Inferring neuronal selectivities from fMR-A, however, requires an understanding of the relationship between the stimulus selectivity of neuronal adaptation and responses. We studied this relationship by recording single cells in macaque inferior temporal (IT) cortex, an area that shows fMRI adaptation. Repetition of identical object images reduced the responsiveness of single IT neurons. Presentation of an image to which the neuron was unresponsive did not alter the response to a subsequent image that activated the neuron. Successive presentation of two different images to which the neuron responded similarly produced adaptation, but less so than the repeated presentation of an image. The neuronal adaptation at the single-cell level showed a greater degree of stimulus selectivity than the responses. This complicates the interpretation of fMR-A paradigms when inferring neuronal selectivity.

Adaptation, Physiological↗

Mapping the parietal cortex of human and non-human primates.

The present essay reviews a series of functional magnetic resonance imaging (fMRI) studies conducted in parallel in humans and awake monkeys, concentrating on the intraparietal sulcus (IPS). MR responses to a range of visual stimuli indicate that the human IPS contains more functional regions along its anterior-posterior extent than are known in the monkey. Human IPS includes four motion sensitive regions, ventral IPS (VIPS), parieto-occipital IPS (POIPS), dorsal IPS medial (DIPSM) and dorsal IPS anterior (DIPSA), which are also sensitive to three-dimensional structure from motion (3D SFM). On the other hand, the monkey IPS contains only one motion sensitive area (VIP), which is not particularly sensitive to 3D SFM. The human IPS includes four regions sensitive to two-dimensional shape and three representations of central vision, while monkey IPS appears to contain only two shape sensitive regions and one central representation. These data support the hypothesis that monkey LIP corresponds to the region of human IPS between DIPSM and POIPS and that a portion of the anterior part of human IPS is evolutionarily new. This additional cortical tissue may provide the capacity for an enhanced visual analysis of moving images necessary for sophisticated control of manipulation and tool handling.

Animals↗

Processing of kinetic boundaries in macaque V4.

We used gratings and shapes defined by relative motion to study selectivity for static kinetic boundaries in macaque V4 neurons. Kinetic gratings were generated by random pixels moving in opposite directions in the neighboring bars, either parallel to the orientation of the boundary (parallel kinetic grating) or perpendicular to the boundary (orthogonal kinetic grating). Neurons were also tested with static, luminance defined gratings to establish cue invariance. In addition, we used eight shapes defined either by relative motion or by luminance contrast, as used previously to test cue invariance in the infero-temporal (IT) cortex. A sizeable fraction (10-20%) of the V4 neurons responded selectively to kinetic patterns. Most neurons selective for kinetic contours had receptive fields (RFs) within the central 10 degrees of the visual field. Neurons selective for the orientation of kinetic gratings were defined as having similar orientation preferences for the two types of kinetic gratings, and the vast majority of these neurons also retained the same orientation preference for luminance defined gratings. Also, kinetic shape selective neurons had similar shape preferences when the shape was defined by relative motion or by luminance contrast, showing a cue-invariant form processing in V4. Although shape selectivity was weaker in V4 than what has been reported in the IT cortex, cue invariance was similar in the two areas, suggesting that invariance for luminance and motion cues of IT originates in V4. The neurons selective for kinetic patterns tended to be clustered within dorsal V4.

Animals↗

Observing others: multiple action representation in the frontal lobe.

Observation of actions performed by others activates monkey ventral premotor cortex, where action meaning, but not object identity, is coded. In a functional MRI (fMRI) study, we investigated whether other monkey frontal areas respond to actions performed by others. Observation of a hand grasping objects activated four frontal areas: rostral F5 and areas 45B, 45A, and 46. Observation of an individual grasping an object also activated caudal F5, which indicates different degrees of action abstraction in F5. Observation of shapes activated area 45, but not premotor F5. Convergence of object and action information in area 45 may be important for full comprehension of actions.

Animals↗

Convergence of depth from texture and depth from disparity in macaque inferior temporal cortex.

The visual system must reconstruct the three-dimensional structure of an object from two-dimensional retinal images. Previous research has shown that macaque inferior temporal (IT) neurons, although belonging to the ventral visual stream, code for depth defined by binocular disparity gradients. Here, we demonstrate that macaque IT neurons also code for depth defined by texture gradients, a monocular depth cue. Single IT neurons were selective for the tilt of texture-defined surfaces, and the tilt preferences of individual neurons remained the same, whether surfaces were defined by texture or disparity cues. Furthermore, the tilt preference was invariant over different types of textures and slants, suggesting an abstract representation of surface tilt in ventral visual cortex.

Animals↗

Color discrimination involves ventral and dorsal stream visual areas.

We used positron emission tomography (PET) and functional magnetic resonance imaging (fMRI) in human subjects to investigate whether the ventral and dorsal visual stream cooperate when active judgements about color have to be made. Color was used as the attribute, because it is processed primarily in the ventral stream. The centrally positioned stimuli were equiluminant shades of brown. The successive color discrimination task was contrasted to a dimming detection task, in which retinal input was identical but with double the number of motor responses. The stimulus presentation rate was parametrically varied and a constant performance level was obtained for all conditions. The visual activation sites were identified by retinotopic mapping and cortical flattening. In addition, one psychophysical and two fMRI experiments were performed to control for differences in visuospatial attention and motor output. Successive color discrimination involved early visual areas, including V1 and VP and the ventral color-responsive region, as well as anterior and middle dorsal intraparietal sulcus, dorsal premotor cortex and pre-SMA. Cortical regions involved in dimming detection and motor output included area V3A, hMT/V5+, lateral occipital sulcus, posterior dorsal intraparietal sulcus, primary motor cortex and SMA. These experiments demonstrated that even with color as the attribute, successive discrimination, in which a decision process has to link visual signals to motor responses, involves both ventral and dorsal visual stream areas.

Adult↗

The processing of visual shape in the cerebral cortex of human and nonhuman primates: a functional magnetic resonance imaging study.

We compared neural substrates of two-dimensional shape processing in human and nonhuman primates using functional magnetic resonance (MR) imaging in awake subjects. The comparison of MR activity evoked by viewing intact and scrambled images of objects revealed shape-sensitive regions in occipital, temporal, and parietal cortex of both humans and macaques. Intraparietal cortex in monkeys was relatively more two-dimensional shape sensitive than that of humans. In both species, there was an interaction between scrambling and type of stimuli (grayscale images and drawings), but the effect of stimulus type was much stronger in monkeys than in humans. Shape- and motion-sensitive regions overlapped to some degree. However, this overlap was much more marked in humans than in monkeys. The shape-sensitive regions can be used to constrain the warping of monkey to human cortex and suggest a large expansion of lateral parietal and superior temporal cortex in humans compared with monkeys.

Adult↗

Comparative mapping of higher visual areas in monkeys and humans.

The advent of functional magnetic resonance imaging (fMRI) in non-human primates has facilitated comparison of the neurobiology of cognitive functions in humans and macaque monkeys, the most intensively studied animal model for higher brain functions. Most of these comparative studies have been performed in the visual system. The early visual areas V1, V2 and V3, as well as the motion area MT are conserved in humans. Beyond these areas, differences between human and monkey functional organization are increasingly evident. At the regional level, the monkey inferotemporal and intraparietal complexes appear to be conserved in humans, but there are profound functional differences in the intraparietal cortex suggesting that not all its constituent areas are homologous. In the long term, fMRI offers opportunities to compare the functional anatomy of a variety of cognitive functions in the two species.

Animals↗

Search for color 'center(s)' in macaque visual cortex.

It is often stated that color is selectively processed in cortical area V4, in both macaques and humans. However most recent data suggests that color is instead processed in region(s) antero-ventral to V4. Here we tested these two hypotheses in macaque visual cortex, where 'V4' was originally defined, and first described as color selective. Activity produced by equiluminant color-varying (versus luminance-varying) gratings was measured using double-label deoxyglucose in awake fixating macaques, in multiple areas of flattened visual cortex. Much of cortex was activated near-equally by both color- and luminance-varying stimuli. In remaining cortical regions, discrete color-biased columns were found in many cortical visual areas, whereas luminance-biased activity was found in only a few specific regions (V1 layer 4B and area MT). Consistent with a recent hypothesis, V4 was not uniquely specialized for color processing, but areas located antero-ventral to V4 (in/near TEO and anterior TE) showed more color-biased activity.

Animals↗

Perception of three-dimensional shape from specular highlights, deformations of shading, and other types of visual information.

There have been numerous computational models developed in an effort to explain how the human visual system analyzes three-dimensional (3D) surface shape from patterns of image shading, but they all share some important limitations. Models that are applicable to individual static images cannot correctly interpret regions that contain specular highlights, and those that are applicable to moving images have difficulties when a surface moves relative to its sources of illumination. Here we describe a psychophysical experiment that measured the sensitivity of human observers to small differences of 3D shape over a wide variety of conditions. The results provide clear evidence that the presence of specular highlights or the motions of a surface relative to its light source do not pose an impediment to perception, but rather, provide powerful sources of information for the perceptual analysis of 3D shape.

Depth Perception↗

Visual activation in prefrontal cortex is stronger in monkeys than in humans.

The prefrontal cortex supports many cognitive abilities, which humans share to some degree with monkeys. The specialized functions of the prefrontal cortex depend both on the nature of its inputs from other brain regions and on distinctive aspects of local processing. We used functional MRI to compare prefrontal activity between monkey and human subjects when they viewed identical images of objects, either intact or scrambled. Visual object-related activation of the lateral prefrontal cortex was observed in both species, but was stronger in monkeys than in humans, both in magnitude (factors 2-3) and in spatial extent (fivefold or more as a percentage of prefrontal volume). This difference was observed for two different stimulus sets, at two field strengths, and over a range of tasks. These results suggest that there may be more volitional control over visual processing in humans than in monkeys.

Animals↗

Attention to 3-D shape, 3-D motion, and texture in 3-D structure from motion displays.

We used fMRI to directly compare the neural substrates of three-dimensional (3-D) shape and motion processing for realistic textured objects rotating in depth. Subjects made judgments about several different attributes of these objects, including 3-D shape, the 3-D motion, and the scale of surface texture. For all of these tasks, we equated visual input, motor output, and task difficulty, and we controlled for differences in spatial attention. Judgments about 3-D shape from motion involve both parietal and occipito-temporal regions. The processing of 3-D shape is associated with the analysis of 3-D motion in parietal regions and the analysis of surface texture in occipito-temporal regions, which is consistent with the different behavioral roles that are typically attributed to the dorsal and ventral processing streams.

Adult↗

A higher order motion region in human inferior parietal lobule: evidence from fMRI.

The proposal that motion is processed by multiple mechanisms in the human brain has received little anatomical support so far. Here, we compared higher- and lower-level motion processing in the human brain using functional magnetic resonance imaging. We observed activation of an inferior parietal lobule (IPL) motion region by isoluminant red-green gratings when saliency of one color was increased and by long-range apparent motion at 7 Hz but not 2 Hz. This higher order motion region represents the entire visual field, while traditional motion regions predominantly process contralateral motion. Our results suggest that there are two motion-processing systems in the human brain: a contralateral lower-level luminance-based system, extending from hMT/V5+ into dorsal IPS and STS, and a bilateral higher-level saliency-based system in IPL.

Adult↗

The retinotopic organization of primate dorsal V4 and surrounding areas: A functional magnetic resonance imaging study in awake monkeys.

Using functional magnetic resonance imaging (fMRI), we mapped the retinotopic organization throughout the visual cortex of fixating monkeys. The retinotopy observed in areas V1, V2, and V3 was completely consistent with the classical view. V1 and V3 were bordered rostrally by a vertical meridian representation, and V2 was bordered by a horizontal meridian. More anterior in occipital cortex, both areas V3A and MT-V5 had lower and upper visual field representations split by a horizontal meridian. The rostral border of dorsal V4 was characterized by the gradual transition of a representation of the vertical meridian (dorsally) to a representation of the horizontal meridian (more ventrally). Central and ventral V4, on the other hand, were rostrally bordered by a representation of the horizontal meridian. The eccentricity lines ran perpendicular to the ventral V3-V4 border but were parallel to the dorsal V3-V4 border. These results indicate different retinotopic organizations within dorsal and ventral V4, suggesting that the latter regions may not be merely the lower and upper visual field representations of a single area. Moreover, because the present fMRI data are in agreement with previously published electrophysiological results, reported distinctions in the retinotopic organization of human and monkey dorsal V4 reflect genuine species differences that cannot be attributed to technical confounds. Finally, aside from dorsal V4, the retinotopic organization of macaque early visual cortex (V1, V2, V3, V3A, and ventral V4) is remarkably similar to that observed in human fMRI studies. This finding indicates that early visual cortex is mostly conserved throughout hominid evolution.

Anesthesia↗

Stereopsis activates V3A and caudal intraparietal areas in macaques and humans.

Stereopsis, the perception of depth from small differences between the images in the two eyes, provides a rich model for investigating the cortical construction of surfaces and space. Although disparity-tuned cells have been found in a large number of areas in macaque visual cortex, stereoscopic processing in these areas has never been systematically compared using the same stimuli and analysis methods. In order to examine the global architecture of stereoscopic processing in primate visual cortex, we studied fMRI activity in alert, fixating human and macaque subjects. In macaques, we found strongest activation to near/far compared to zero disparity in areas V3, V3A, and CIPS. In humans, we found strongest activation to the same stimuli in areas V3A, V7, the V4d topolog (V4d-topo), and a caudal parietal disparity region (CPDR). Thus, in both primate species a small cluster of areas at the parieto-occipital junction appears to be specialized for stereopsis.

Animals↗