11Object recognition relies on different transformations of the retinal input, ranging from local 12 contrast to object shape and category. While some of those representations are thought to occur 13 at specific stages of the visual hierarchy, many of them are correlated (e.g., object shape and 14 identity) and can be retrieved from the activity of several brain regions. This overlap may be 15 explained either by collinearity across representations, or may instead reflect the coding of 16 multiple dimensions by the same cortical population. Moreover, orthogonal and shared 17 components may differently impact on distinctive stages of the visual hierarchy. We recorded 18 functional MRI (fMRI) activity while participants passively attended to objects, and employed a 19 statistical approach that partition orthogonal and shared object representations to reveal their 20 relative impact on brain processing. Orthogonal shape representations (i.e., silhouette, curvature 21 and medial-axis) independently explain distinct and overlapping clusters of selectivity in 22 occitotemporal (OTC) and parietal cortex. Moreover, we showed that the relevance of shared 23 representations linearly increases moving from posterior to anterior regions. These results 24 indicate that the visual cortex encodes shared relations between different features in a 25 topographic fashion and that object shape is encoded along different dimensions, each 26 representing orthogonal features. 27 28
New & Noteworthy 29While we always have available a general sense of what 'a shape is', what is the 30 computational counterpart of this immediate percept? Here, we employed three competing shape 31 models to explain brain representations when viewing real objects. We found that object shape is 32 encoded in a multi-dimensional fashion and thus defined by the interaction of multiple features. 33 34 Bracci S, and Op de Beeck H. Dissociations and Associations between Shape and Category 491 Representations in the Two Visual Pathways. J Neurosci 36: 432-444, 2016. 492 Bracci S, Ritchie JB, Kalfas I, and Op de Beeck H. The ventral visual pathway represents animal 493 appearance over animacy, unlike human behavior and deep neural networks. J Neurosci 2019. 494 Brincat SL, and Connor CE. Underlying principles of visual shape selectivity in posterior 495 inferotemporal cortex. Nat Neurosci 7: 880-886, 2004. 496 Cadieu C, Kouh M, Pasupathy A, Connor CE, Riesenhuber M, and Poggio T. A model of V4 shape 497 selectivity and invariance. J Neurophysiol 98: 1733-1750, 2007. 498 Cahalane DJ, Charvet CJ, and Finlay BL. Systematic, balancing gradients in neuron density and 499 number across the primate isocortex. Front Neuroanat 6: 28, 2012. 500 Caldara R, Seghier ML, Rossion B, Lazeyras F, Michel C, and Hauert CA. The fusiform face area is 501 tuned for curvilinear patterns with more high-contrasted elements in the upper part. Neuroimage 502 31: 313-319, 2006. 503 Carlson ET, Rasquinha RJ, Zhang K, and Connor CE. A sparse object coding scheme in area V4. Curr 504 Biol 21: 288...