scholarly journals The Representation of Objects in the Human Occipital and Temporal Cortex

2000 ◽  
Vol 12 (supplement 2) ◽  
pp. 35-51 ◽  
Author(s):  
Alumit Ishai ◽  
Leslie G. Ungerleider ◽  
Alex Martin ◽  
James V. Haxby

Recently, we identified, using fMRI, three bilateral regions in the ventral temporal cortex that responded preferentially to faces, houses, and chairs [Ishai, A., Ungerleider, L. G., Martin, A., Schouten, J. L., & Haxby, J. Y. (1999). Distributed representation of objects in the human ventral visual pathway. Proceedings of the National Academy of Sciences, U.S.A., 96, 9379-9384]. Here, we report differential patterns of activation, similar to those seen in the ventral temporal cortex, in bilateral regions of the ventral occipital cortex. We also found category-related responses in the dorsal occipital cortex and in the superior temporal sulcus. Moreover, rather than activating discrete, segregated areas, each category was associated with its own differential pattern of response across a broad expanse of cortex. The distributed patterns of response were similar across tasks (passive viewing, delayed matching) and presentation formats (photographs, line drawings). We propose that the representation of objects in the ventral visual pathway, including both occipital and temporal regions, is not restricted to small, highly selective patches of cortex but, instead, is a distributed representation of information about object form. Within this distributed system, the representation of faces appears to be less extensive as compared to the representations of nonface objects.

2002 ◽  
Vol 87 (4) ◽  
pp. 1960-1973 ◽  
Author(s):  
Masayuki Watanabe ◽  
Hiroki Tanaka ◽  
Takanori Uka ◽  
Ichiro Fujita

Area V4 is an intermediate stage of the ventral visual pathway providing major input to the final stages in the inferior temporal cortex (IT). This pathway is involved in the processing of shape, color, and texture. IT neurons are also sensitive to horizontal binocular disparity, suggesting that binocular disparity is processed along the ventral visual pathway. In the present study, we examined the processing of binocular disparity information by V4 neurons. We recorded responses of V4 neurons to binocularly disparate stimuli. A population of V4 neurons modified their responses according to changes of stimulus disparity; neither monocular responses nor eye movements could account for this modulation. Disparity-tuning curves were similar for different locations within a neuron's receptive field. Neighboring neurons recorded using a single electrode displayed similar disparity-tuning properties. These findings indicate that a population of V4 neurons is selective for binocular disparity, invariant for the position of the stimulus within the receptive field. The finding that V4 neurons with similar disparity selectivity are clustered suggests the existence of functional modules for disparity processing in V4.


1999 ◽  
Vol 96 (16) ◽  
pp. 9379-9384 ◽  
Author(s):  
A. Ishai ◽  
L. G. Ungerleider ◽  
A. Martin ◽  
J. L. Schouten ◽  
J. V. Haxby

Author(s):  
Edward H. Silson ◽  
Iris I. A. Groen ◽  
Chris I. Baker

AbstractHuman visual cortex is organised broadly according to two major principles: retinotopy (the spatial mapping of the retina in cortex) and category-selectivity (preferential responses to specific categories of stimuli). Historically, these principles were considered anatomically separate, with retinotopy restricted to the occipital cortex and category-selectivity emerging in the lateral-occipital and ventral-temporal cortex. However, recent studies show that category-selective regions exhibit systematic retinotopic biases, for example exhibiting stronger activation for stimuli presented in the contra- compared to the ipsilateral visual field. It is unclear, however, whether responses within category-selective regions are more strongly driven by retinotopic location or by category preference, and if there are systematic differences between category-selective regions in the relative strengths of these preferences. Here, we directly compare contralateral and category preferences by measuring fMRI responses to scene and face stimuli presented in the left or right visual field and computing two bias indices: a contralateral bias (response to the contralateral minus ipsilateral visual field) and a face/scene bias (preferred response to scenes compared to faces, or vice versa). We compare these biases within and between scene- and face-selective regions and across the lateral and ventral surfaces of the visual cortex more broadly. We find an interaction between surface and bias: lateral surface regions show a stronger contralateral than face/scene bias, whilst ventral surface regions show the opposite. These effects are robust across and within subjects, and appear to reflect large-scale, smoothly varying gradients. Together, these findings support distinct functional roles for the lateral and ventral visual cortex in terms of the relative importance of the spatial location of stimuli during visual information processing.


2020 ◽  
Author(s):  
Iris I A Groen ◽  
Edward H Silson ◽  
David Pitcher ◽  
Chris I Baker

AbstractHuman visual cortex contains three scene-selective regions in the lateral, medial and ventral cortex, termed the occipital place area (OPA), medial place area (MPA) and parahippocampal place area (PPA). Using functional magnetic resonance imaging (fMRI), all three regions respond more strongly when viewing visual scenes compared with isolated objects or faces. To determine how these regions are functionally and causally connected, we applied transcranial magnetic stimulation to OPA and measured fMRI responses before and after stimulation, using a theta-burst paradigm (TBS). To test for stimulus category-selectivity, we presented a range of visual categories (scenes, buildings, objects, faces). To test for specificity of any effects to TBS of OPA we employed two control conditions: Sham, with no TBS stimulation, and an active TBS-control with TBS to a proximal face-selective cortical region (occipital face area, or OFA). We predicted that TBS to OPA (but not OFA) would lead to decreased responses to scenes and buildings (but not other categories) in other scene-selective cortical regions. Across both ROI and whole-volume analyses, we observed decreased responses to scenes in PPA as a result of TBS. However, these effects were neither category specific, with decreased responses to all stimulus categories, nor limited to scene-selective regions, with decreases also observed in face-selective fusiform face area (FFA). Furthermore, similar effects were observed with TBS to OFA, thus effects were not specific to the stimulation site in the lateral occipital cortex. Whilst these data are suggestive of a causal, but non-specific relationship between lateral occipital and ventral temporal cortex, we discuss several factors that could have underpinned this result, such as the differences between TBS and online TMS, the role of anatomical distance between stimulated regions and how TMS effects are operationalised. Furthermore, our findings highlight the importance of active control conditions in brain stimulation experiments to accurately assess functional and causal connectivity between specific brain regions.


2021 ◽  
Author(s):  
Edward H Silson ◽  
Iris Isabelle Anna Groen ◽  
Chris I Baker

Human visual cortex is organised broadly according to two major principles: retinotopy (the spatial mapping of the retina in cortex) and category-selectivity (preferential responses to specific categories of stimuli). Historically, these principles were considered anatomically separate, with retinotopy restricted to the occipital cortex and category-selectivity emerging in lateral-occipital and ventral-temporal cortex. Contrary to this assumption, recent studies show that category-selective regions exhibit systematic retinotopic biases. It is unclear, however, whether responses within these regions are more strongly driven by retinotopic location or by category preference, and if there are systematic differences between category-selective regions in the relative strengths of these preferences. Here, we directly compare spatial and category preferences by measuring fMRI responses to scene and face stimuli presented in the left or right visual field and computing two bias indices: a spatial bias (response to the contralateral minus ipsilateral visual field) and a category bias (response to the preferred minus non-preferred category). We compare these biases within and between scene- and face-selective regions across the lateral and ventral surfaces of visual cortex. We find an interaction between surface and bias: lateral regions show a stronger spatial than category bias, whilst ventral regions show the opposite. These effects are robust across and within subjects, and reflect large-scale, smoothly varying gradients across both surfaces. Together, these findings support distinct functional roles for lateral and ventral category-selective regions in visual information processing in terms of the relative importance of spatial information.


2005 ◽  
Vol 17 (4) ◽  
pp. 580-590 ◽  
Author(s):  
Alice J. O'Toole ◽  
Fang Jiang ◽  
Hervé Abdi ◽  
James V. Haxby

Object and face representations in ventral temporal (VT) cortex were investigated by combining object confusability data from a computational model of object classification with neural response confusability data from a functional neuroimaging experiment. A pattern-based classification algorithm learned to categorize individual brain maps according to the object category being viewed by the subject. An identical algorithm learned to classify an image-based, view-dependent representation of the stimuli. High correlations were found between the confusability of object categories and the confusability of brain activity maps. This occurred even with the inclusion of multiple views of objects, and when the object classification model was tested with high spatial frequency “line drawings” of the stimuli. Consistent with a distributed representation of objects in VT cortex, the data indicate that object categories with shared image-based attributes have shared neural structure.


2020 ◽  
Author(s):  
Shijia Fan ◽  
Xiaosha Wang ◽  
Xiaoying Wang ◽  
Tao Wei ◽  
Yanchao Bi

AbstractVisual object recognition in humans and nonhuman primates is achieved by the ventral visual pathway (ventral occipital-temporal cortex, VOTC), which shows a well-documented object domain structure. An on-going question has been what type of information is processed in higher-order VOTC that underlies such observations, with recent evidence suggesting effects of certain visual features. Combining computational vision models, fMRI experiment using a parametric-modulation approach, and natural image statistics of common objects, we depicted the neural distribution of a comprehensive set of visual features in VOTC, identifying voxel sensitivities to specific feature sets across geometry/shape, Fourier power, and color. The visual feature combination pattern in VOTC is significantly explained by their relationships to different types of response-action computation (Fight-or-Flight, Navigation, and Manipulation), as derived from behavioral ratings and natural image statistics. These results offer the first comprehensive visual featural map in VOTC and a plausible theoretical explanation as a mapping onto different types of downstream response-action systems.


2013 ◽  
Vol 25 (11) ◽  
pp. 1777-1793 ◽  
Author(s):  
Rosemary A. Cowell ◽  
Garrison W. Cottrell

We trained a neurocomputational model on six categories of photographic images that were used in a previous fMRI study of object and face processing. Multivariate pattern analyses of the activations elicited in the object-encoding layer of the model yielded results consistent with two previous, contradictory fMRI studies. Findings from one of the studies [Haxby, J. V., Gobbini, M. I., Furey, M. L., Ishai, A., Schouten, J. L., & Pietrini, P. Distributed and overlapping representations of faces and objects in ventral temporal cortex. Science, 293, 2425–2430, 2001] were interpreted as evidence for the object-form topography model. Findings from the other study [Spiridon, M., & Kanwisher, N. How distributed is visual category information in human occipito-temporal cortex? An fMRI study. Neuron, 35, 1157–1165, 2002] were interpreted as evidence for neural processing mechanisms in the fusiform face area that are specialized for faces. Because the model contains no special processing mechanism or specialized architecture for faces and yet it can reproduce the fMRI findings used to support the claim that there are specialized face-processing neurons, we argue that these fMRI results do not actually support that claim. Results from our neurocomputational model therefore constitute a cautionary tale for the interpretation of fMRI data.


2020 ◽  
Author(s):  
JohnMark Taylor ◽  
Yaoda Xu

AbstractDespite decades of neuroscience research, our understanding of the relationship between color and form processing in the primate ventral visual pathway remains incomplete. Using fMRI multivoxel pattern analysis, this study examined the coding of color with both a simple form feature (orientation) and a mid-level form feature (curvature) in human early visual areas V1 to V4, posterior and central color regions, and shape areas in ventral and lateral occipito-temporal cortex. With the exception of the central color region (which showed color but not form decoding), successful color and form decoding was found in all other regions examined, even for color and shape regions showing univariate sensitivity to one feature. That said, all regions exhibited significant feature decoding biases, with decoding from color and shape regions largely consistent with their univariate preferences. Color and form are thus represented in neither a completely distributed nor a completely modular manner, but a biased distributed manner. Interestingly, coding of one feature in a brain region was always tolerant to changes in the other feature, indicating relative independence of color and form coding throughout the ventral visual cortex. Although evidence for interactive coding of color and form also existed, the effect was weak and only existed for color and orientation conjunctions in early visual cortex. No evidence for interactive coding of color and curvature was found. The predominant relationship between color and form coding in the human brain appears to be one of anatomical coexistence (in a biased distributed manner), but representational independence.


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