Abstract

Neurons at primary visual cortex (V1) in humans and other species are edge filters organized in orientation maps. In these maps, neurons with similar orientation preference are clustered together in iso-orientation domains. These maps have two fundamental properties: (1) retinotopy, i.e. correspondence between displacements at the image space and displacements at the cortical surface, and (2) a trade-off between good coverage of the visual field with all orientations and continuity of iso-orientation domains in the cortical space. There is an active debate on the origin of these locally continuous maps. While most of the existing descriptions take purely geometric/mechanistic approaches which disregard the network function, a clear exception to this trend in the literature is the original approach of Hyvärinen and Hoyer based on infomax and Topographic Independent Component Analysis (TICA). Although TICA successfully addresses a number of other properties of V1 simple and complex cells, in this work we question the validity of the orientation maps obtained from TICA. We argue that the maps predicted by TICA can be analyzed in the retinal space, and when doing so, it is apparent that they lack the required continuity and retinotopy. Here we show that in the orientation maps reported in the TICA literature it is easy to find examples of violation of the continuity between similarly tuned mechanisms in the retinal space, which suggest a random scrambling incompatible with the maps in primates. The new experiments in the retinal space presented here confirm this guess: TICA basis vectors actually follow a random salt-and-pepper organization back in the image space. Therefore, the interesting clusters found in the TICA topology cannot be interpreted as the actual cortical orientation maps found in cats, primates or humans. In conclusion, Topographic ICA does not reproduce cortical orientation maps.

Highlights

  • Retinotopy, continuity and coverage in V1 orientation mapsNeurons at the primary visual cortex in mammals are localized edge filters, i.e. their receptive fields are tuned to certain orientation at certain retinal location [1, 2]

  • In this work we elaborate on this open question: we argue that a biological interpretation of the predicted clusters would require a smoother retinotopic relation between the retinal space and the Topographic Independent Component Analysis (TICA) topology, because, as Topographic Independent Component Analysis (ICA) reveals random scrambling of orientation in visual space opposed to the animals with map patterns, the TICA orientation maps does not have an appropriate counterpart in the image domain with locally continuous structure

  • Given the straightforward relation between cortical location and spatial tuning in the visual field, Fig 1, a proper theory should lead to locally continuous orientation domains in the retinal space

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Summary

Introduction

Retinotopy, continuity and coverage in V1 orientation mapsNeurons at the primary visual cortex in mammals are localized edge filters, i.e. their receptive fields are tuned to certain orientation at certain retinal location [1, 2]. The large scale organization of the V1 surface is retinotopic, i.e. the retinal space is mapped onto the cortical space so that neighbor cells in the V1 surface are tuned to close regions in the visual field [3,4,5,6]. Retinotopy refers to the correspondence between the location of the receptive field at the retinal space and the location of the neuron at the cortex. For some species like cats, primates and humans, on top of retinotopy, V1 cells have a quite special arrangement: the so called orientation maps. In these maps, neurons with similar orientation preference are clustered together in the so called iso-orientation domains

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