The Detection of Orientation of Small Objects

Perception ◽  
1997 ◽  
Vol 26 (1_suppl) ◽  
pp. 59-59
Author(s):  
J M Zanker ◽  
M P Davey

Visual information processing in primate cortex is based on a highly ordered representation of the surrounding world. In addition to the retinotopic mapping of the visual field, systematic variations of the orientation tuning of neurons are described electrophysiologically for the first stages of the visual stream. On the way to understanding the relation of position and orientation representation, in order to give an adequate account of cortical architecture, it will be an essential step to define the minimum spatial requirements for detection of orientation. We addressed the basic question of spatial limits for detecting orientation by comparing computer simulations of simple orientation filters with psychophysical experiments in which the orientation of small lines had to be detected at various positions in the visual field. At sufficiently high contrast levels, the minimum physical length of a line whose orientation can just be resolved is not constant when presented at various eccentricities, but covaries inversely with the cortical magnification factor. A line needs to span less than 0.2 mm on the cortical surface in order to be recognised as oriented, independently of the actual eccentricity at which the stimulus is presented. This seems to indicate that human performance for this task approaches the physical limits, requiring hardly more than approximately three input elements to be activated, in order to detect the orientation of a highly visible line segment. Combined with the estimates for receptive field sizes of orientation-selective filters derived from computer simulations, this experimental result may nourish speculations of how the rather local elementary process underlying orientation detection in the human visual system can be assembled to form much larger receptive fields of the orientation-sensitive neurons known to exist in the primate visual system.

Perception ◽  
1998 ◽  
Vol 27 (2) ◽  
pp. 167-181
Author(s):  
Johannes M Zanker

First steps of visual-information processing in primates are characterised by a highly ordered representation of the outside world on the cortex. Two prominent features of cortical organisation are the retinotopic mapping of position in the visual field on the first stages of the visual stream, and the systematic variation of orientation preference in the same areas. In an attempt to understand the relation of position and orientation representation, we need to know the minimum spatial requirements for orientation detection. In the present paper, the spatial limits for detecting orientation are analysed by simulating simple orientation filters and testing the ability of human observers to detect the orientation of small lines at various positions in the visual field. At sufficiently high contrast levels, the minimum physical length of a line to discriminate orientation differences of 45°–90° is not constant when presented at various eccentricities, but covaries inversely with the cortical magnification factor. In consequence, a line needs to correspond to about 0.2 mm of cortical surface, independently of the actual eccentricity at which the stimulus is presented, in order to allow observers to recognise its orientation. This has consequences for our understanding of orientation detection, (i) In combination with simulation experiments, it becomes clear that the elementary process underlying orientation detection is a local operation, which seems to focus on small regions compared with cortical receptive fields, (ii) With respect to the number of inputs to the visual cortex, the performance of this local operation approaches the physical limits, requiring hardly more than three-four input LGN axons to be activated for detecting the orientation of a highly visible line segment. Comparing these spatial characteristics with the receptive fields of orientation-sensitive neurons in the primate visual system could suggest new insights into the neuronal circuits underlying orientation mapping in the human cortex.


1978 ◽  
Vol 41 (2) ◽  
pp. 285-304 ◽  
Author(s):  
A. Antonini ◽  
G. Berlucchi ◽  
J. M. Sprague

1. In agreement with previous work, we have found that the ipsilateral visual field is represented in an extensive rostral portion--from one-third to one-half--of the superior colliculus (SC) of the cat. This representation is binocular. The SC representation of the ipsilateral visual field can be mediated both directly, by crossed retinotectal connections originating from temporal hemiretina, and indirectly, by across-the-midline connections relaying visual information from one-half of the brain to contralateral SC. 2. In order to study the indirect, across-the-midline visual input to the SC, we have recorded responses of SC neurons to visual stimuli presented to either the ipsilateral or the contralateral eye of cats with a midsagittal splitting of the optic chiasm. Units driven by the ipsilateral eye, presumably through the direct retinotectal input and/or corticotectal connections from ipsilateral visual cortex, were found throughout the SC, except at its caudal pole, which normally receives fibers from the extreme periphery of the contralateral nasal hemiretina. Units driven by the contralateral eye, undoubtedly through an indirect across-the-midline connection, were found only in the anterior portion of the SC, in which is normally represented the ipsilateral visual field. Receptive fields in both ipsilateral and contralateral eye had properties typical of SC receptive fields in cats with intact optic pathways. 3. All units having a receptive field in the contralateral eye had also a receptive field in the ipsilateral eye; for each of these units, the receptive fields in both eyes invariably abutted the vertical meridian of the visual field. The receptive field in one eye had about the same elevation relative to the horizontal meridian and the same vertical extension as the receptive field in the other eye; the two receptive fields of each binocular unit matched each other at the vertical meridian and formed a combined receptive field straddling the vertical midline of the horopter...


Author(s):  
Brian Rogers

‘The physiology and anatomy of the visual system’ describes what we have learned from neurophysiology and anatomy over the past eighty years and what this tells us about the meaning of the circuits involved in visual information processing. It explains how psychologists and physiologists use the terms ‘mechanism’ and ‘process’. For physiologists, a mechanism is linked to the actions of individual neurons, neural pathways, and the ways in which the neurons are connected up. For psychologists, the term is typically used to describe the processes the neural circuits may carry out. The human retina is described with explanations of lateral inhibition, receptive fields, and feature detectors as well as the visual cortex and different visual pathways.


1979 ◽  
Vol 42 (1) ◽  
pp. 137-152 ◽  
Author(s):  
A. Antonini ◽  
G. Berlucchi ◽  
C. A. Marzi ◽  
J. M. Sprague

1. Section of the posterior two-thirds of the corpus callosum eliminates almost completely the response of superior colliculus (SC) neurons to stimulation of the contralateral eye in split-chiasm cats. On the contrary, the responsiveness of SC neurons to stimulation of the contralateral eye is not abolished by a transection of the posterior and tectal commissures leaving the corpus callosum intact. The callosal section also reduces the number of SC receptive fields abutting the vertical meridian in the ipsilateral eye of split-chiasm cats. 2. In cats with intact optic pathways, a similar callosal section abolishes the SC representation of the ipsilateral visual field in the ipsilateral eye and also reduces the number of receptive fields adjoining the vertical meridian in the same eye. In the contralateral eye, the SC representation of the ipsilateral visual field is reduced in extension to about one-fifth of that seen in cats with intact commissures. 3. The results suggest that the corpus callosum is the main pathway for cross-midline communication of visual information at not only the cortical, but also the midbrain level. The corpus callosum may subserve this function because it contains uninterrupted crossed corticotectal projections or because it transmits visual information from one hemisphere to contralateral cortical areas projecting ipsilaterally to SC. The latter hypothesis is more likely but, in any case, the findings imply that the lack of interhemispheric transfer of visual learning in cats with a chiasmatic and callosal section may depend on a midline disconnection of both subcortical and cortical visual centers. 4. The corpus callosum is also responsible for the representation of the ipsilateral visual field of the ipsilateral eye in the cat SC. The SC representation of the ipsilateral visual field in the contralateral eye is due, in minimal part, to direct retinotectal connections from temporal retina and, for the largest part, to the corpus callosum. 5. Finally, the corpus callosum contributes to the representation of the contralateral visual field near the vertical meridian of the temporal retina in both split-chiasm and normal cats. This is probably due to the scarcity of direct retinotectal projections from this part of the retina and to their supplementation by corticotectal neurons influenced by the callosal afferents.


2017 ◽  
Author(s):  
Jesse Gomez ◽  
Vaidehi Natu ◽  
Brianna Jeska ◽  
Michael Barnett ◽  
Kalanit Grill-Spector

ABSTRACTReceptive fields (RFs) processing information in restricted parts of the visual field are a key property of neurons in the visual system. However, how RFs develop in humans is unknown. Using fMRI and population receptive field (pRF) modeling in children and adults, we determined where and how pRFs develop across the ventral visual stream. We find that pRF properties in visual field maps, V1 through VO1, are adult-like by age 5. However, pRF properties in face- and word-selective regions develop into adulthood, increasing the foveal representation and the visual field coverage for faces in the right hemisphere and words in the left hemisphere. Eye-tracking indicates that pRF changes are related to changing fixation patterns on words and faces across development. These findings suggest a link between viewing behavior of faces and words and the differential development of pRFs across visual cortex, potentially due to competition on foveal coverage.


1990 ◽  
Vol 5 (5) ◽  
pp. 489-495 ◽  
Author(s):  
Douglas R. Wylie ◽  
Barrie J. Frost

AbstractPrevious electrophysiological studies have shown that neurons in the nucleus of the basal optic root (nBOR) of the pigeon respond best to wholefield stimuli moving slowly in a particular direction in the contralateral visual field. In this study, we have found that some nBOR neurons respond to wholefield stimulation of both eyes. These binocular neurons have spatially separate receptive fields in both visual fields. Some binocular neurons prefer the same direction of wholefield motion in both eyes, and thus respond best to wholefield visual motion which would result from translation movements of the bird, either ascent, descent, or forward and backward motion. Other neurons prefer opposite directions of wholefield motion in each eye and therefore respond optimally to wholefield visual motion simulating rotational movements of the bird, either roll or yaw. These binocular neurons may play a crucial part in the locomotor behavior of the pigeon by providing visual information distinguishing translational and rotational movements.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Sonia Poltoratski ◽  
Kendrick Kay ◽  
Dawn Finzi ◽  
Kalanit Grill-Spector

AbstractSpatial processing by receptive fields is a core property of the visual system. However, it is unknown how spatial processing in high-level regions contributes to recognition behavior. As face inversion is thought to disrupt typical holistic processing of information in faces, we mapped population receptive fields (pRFs) with upright and inverted faces in the human visual system. Here we show that in face-selective regions, but not primary visual cortex, pRFs and overall visual field coverage are smaller and shifted downward in response to face inversion. From these measurements, we successfully predict the relative behavioral detriment of face inversion at different positions in the visual field. This correspondence between neural measurements and behavior demonstrates how spatial processing in face-selective regions may enable holistic perception. These results not only show that spatial processing in high-level visual regions is dynamically used towards recognition, but also suggest a powerful approach for bridging neural computations by receptive fields to behavior.


2017 ◽  
Vol 34 ◽  
Author(s):  
REECE MAZADE ◽  
JOSE MANUEL ALONSO

AbstractVisual information reaches the cerebral cortex through a major thalamocortical pathway that connects the lateral geniculate nucleus (LGN) of the thalamus with the primary visual area of the cortex (area V1). In humans, ∼3.4 million afferents from the LGN are distributed within a V1 surface of ∼2400 mm2, an afferent number that is reduced by half in the macaque and by more than two orders of magnitude in the mouse. Thalamocortical afferents are sorted in visual cortex based on the spatial position of their receptive fields to form a map of visual space. The visual resolution within this map is strongly correlated with total number of thalamic afferents that V1 receives and the area available to sort them. The ∼20,000 afferents of the mouse are only sorted by spatial position because they have to cover a large visual field (∼300 deg) within just 4 mm2 of V1 area. By contrast, the ∼500,000 afferents of the cat are also sorted by eye input and light/dark polarity because they cover a smaller visual field (∼200 deg) within a much larger V1 area (∼400 mm2), a sorting principle that is likely to apply also to macaques and humans. The increased precision of thalamic sorting allows building multiple copies of the V1 visual map for left/right eyes and light/dark polarities, which become interlaced to keep neurons representing the same visual point close together. In turn, this interlaced arrangement makes cortical neurons with different preferences for stimulus orientation to rotate around single cortical points forming a pinwheel pattern that allows more efficient processing of objects and visual textures.


Perception ◽  
10.1068/p7392 ◽  
2012 ◽  
Vol 41 (11) ◽  
pp. 1355-1372 ◽  
Author(s):  
David C Burr ◽  
Maria Concetta Morrone

To interact rapidly and effectively with our environment, our brain needs access to a neural representation—or map—of the spatial layout of the external world. However, the construction of such a map poses major challenges to the visual system, given that the images on our retinae depend on where the eyes are looking, and shift each time we move our eyes, head, and body to explore the world. Much research has been devoted to how the stability is achieved, with the debate often polarized between the utility of spatiotopic maps (that remain solid in external coordinates), as opposed to transiently updated retinotopic maps. Our research suggests that the visual system uses both strategies to maintain stability. f MRI, motion-adaptation, and saccade-adaptation studies demonstrate and characterize spatiotopic neural maps within the dorsal visual stream that remain solid in external rather than retinal coordinates. However, the construction of these maps takes time (up to 500 ms) and attentional resources. To solve the immediate problems created by individual saccades, we postulate the existence of a separate system to bridge each saccade with neural units that are ‘transiently craniotopic’. These units prepare for the effects of saccades with a shift of their receptive fields before the saccade starts, then relaxing back into their standard position during the saccade, compensating for its action. Psychophysical studies investigating localization of stimuli flashed briefly around the time of saccades provide strong support for these neural mechanisms, and show quantitatively how they integrate information across saccades. This transient system cooperates with the spatiotopic mechanism to provide a useful map to guide interactions with our environment: one rapid and transitory, bringing into play the high-resolution visual areas; the other slow, long-lasting, and low-resolution, useful for interacting with the world.


2020 ◽  
Author(s):  
Sonia Poltoratski ◽  
Kendrick Kay ◽  
Dawn Finzi ◽  
Kalanit Grill-Spector

AbstractSpatial processing by receptive fields is a core property of the visual system. However, it is unknown how spatial coding in high-level regions contributes to recognition behavior. As face inversion is thought to disrupt typical ‘holistic’ processing of information in faces, we mapped population receptive fields (pRFs) with upright and inverted faces in the human visual system. In face-selective regions, but not primary visual cortex, pRFs and overall visual field coverage were smaller and shifted downward in response to face inversion. From these measurements, we successfully predicted the relative behavioral detriment of face inversion at different positions in the visual field. This correspondence between neural measurements and behavior demonstrates how spatial integration in face-selective regions enables holistic processing. These results not only show that spatial processing in high-level visual regions is dynamically used towards recognition, but also suggest a powerful approach for bridging neural computations by receptive fields to behavior.


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