Literature DB >> 418175

The third visual complex of rhesus monkey prestriate cortex.

S M Zeki.   

Abstract

1. Two independent but neighbouring visual areas, V3 and V3A, sharing a common cytoarchitectural plan, but in each one of which the visual fields are separately represented, have been studied anatomically, functionally, and in combined anatomico-physiological experiments. 2. The properties of single cells in the two areas are so similar, judged by the techniques used in this study, that it is often impossible to tell whether any one penetration was sampling from cells in V3 or V3A. This is especially so if the cells have receptive fields in the lower hemi-quadrants, since the vertical meridian of the lower visual fields is represented along the V3-V3A boundary and since a transition from V3 to V3A along this border is not accompanied by a shift in receptive field positions of cells. 3. Since the visual fields, including the vertical meridian, are separately represented in these two areas, and since regions of vertical meridian representation are callosally connected, a simple and certain method of specifying the boundary between V3 and V3A is to examine the degeneration following section of the callosal splenium. A heavy patch of degeneration then marks the V3-V3A boundary. Within this patch, however, is a sub-patch containing fewer callosal fibres, or none at all. The boundary between V3 and V3A was taken to be at this subpatch. 4. Since the horizontal meridian is represented at the V2-V3 boundary, and since V1 projects to both these areas, sending coarse fibres to V3 and fine fibres to V2, it was found that the boundary between V2 and V3 could be precisely drawn by making a lesion in the horizontal meridian representation in V1 and noting where, in the prestriate cortex, fine fibres give way to coarse ones, without an intervening gap. 5. Double tracer anatomical experiments, in which tritiated proline was injected into V1 of animals whose callosal splenium had been sectioned, showed that whereas V3 receives a direct input from V1, V3A does not. V3A, instead, was found to receive an input from V3. Double tracer anatomical experiments were undertaken to study a possible input from V2 to V3A. Although such experiments did not reveal a direct input from V2 to V3A, they were not entirely conclusive. 6. The vast majority of cells in V3 and V3A were binocularly driven, without obvious monocular preferences. Some cells, however, though responding to stimulation of the individual eyes, summated their responses to binocular stimulation. Others responded only when both eyes were simulataneously stimulated. In any oblique penetration, cells preferring binocular stimulation only occurred either singly or in groups. 7. In an oblique penetration, the shift from a cell responding to binocular stimulation only to one responding equally well to stimulation of either eye was not necessarily accompanied by a shift in orientational preferences, shifts in the former...

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Year:  1978        PMID: 418175      PMCID: PMC1282388          DOI: 10.1113/jphysiol.1978.sp012271

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  17 in total

1.  The projections to the superior temporal sulcus from areas 17 and 18 in the rhesus monkey.

Authors:  S M Zeki
Journal:  Proc R Soc Lond B Biol Sci       Date:  1976-04-13

2.  Combined anatomical and electrophysiological studies on the boundary between the second and third visual areas of rhesus monkey cortex.

Authors:  S M Zeki; D R Sandeman
Journal:  Proc R Soc Lond B Biol Sci       Date:  1976-11-12

3.  The representation of the visual field on the cerebral cortex in monkeys.

Authors:  P M DANIEL; D WHITTERIDGE
Journal:  J Physiol       Date:  1961-12       Impact factor: 5.182

4.  Uniformity of monkey striate cortex: a parallel relationship between field size, scatter, and magnification factor.

Authors:  D H Hubel; T N Wiesel
Journal:  J Comp Neurol       Date:  1974-12-01       Impact factor: 3.215

5.  Uniformity and diversity of structure and function in rhesus monkey prestriate visual cortex.

Authors:  S M Zeki
Journal:  J Physiol       Date:  1978-04       Impact factor: 5.182

6.  The topographic organization of rhesus monkey prestriate cortex.

Authors:  D C Essen; S M Zeki
Journal:  J Physiol       Date:  1978-04       Impact factor: 5.182

7.  The cortical projections of foveal striate cortex in the rhesus monkey.

Authors:  S M Zeki
Journal:  J Physiol       Date:  1978-04       Impact factor: 5.182

8.  Visual receptive fields of single striate corical units projecting to the superior colliculus in the cat.

Authors:  L A Palmer; A C Rosenquist
Journal:  Brain Res       Date:  1974-02-15       Impact factor: 3.252

9.  Receptive fields and functional architecture of monkey striate cortex.

Authors:  D H Hubel; T N Wiesel
Journal:  J Physiol       Date:  1968-03       Impact factor: 5.182

10.  Functional organization of a visual area in the posterior bank of the superior temporal sulcus of the rhesus monkey.

Authors:  S M Zeki
Journal:  J Physiol       Date:  1974-02       Impact factor: 5.182

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  29 in total

1.  Functional analysis of V3A and related areas in human visual cortex.

Authors:  R B Tootell; J D Mendola; N K Hadjikhani; P J Ledden; A K Liu; J B Reppas; M I Sereno; A M Dale
Journal:  J Neurosci       Date:  1997-09-15       Impact factor: 6.167

2.  Distribution of corticotectal cells in macaque.

Authors:  T M Lock; J S Baizer; D B Bender
Journal:  Exp Brain Res       Date:  2003-07-08       Impact factor: 1.972

3.  High-resolution mapping of anatomical connections in marmoset extrastriate cortex reveals a complete representation of the visual field bordering dorsal V2.

Authors:  Janelle Jeffs; Frederick Federer; Jennifer M Ichida; Alessandra Angelucci
Journal:  Cereb Cortex       Date:  2012-04-20       Impact factor: 5.357

4.  Cytoarchitectonic mapping of the human dorsal extrastriate cortex.

Authors:  Milenko Kujovic; Karl Zilles; Aleksandar Malikovic; Axel Schleicher; Hartmut Mohlberg; Claudia Rottschy; Simon B Eickhoff; Katrin Amunts
Journal:  Brain Struct Funct       Date:  2012-02-22       Impact factor: 3.270

Review 5.  Brain maps, great and small: lessons from comparative studies of primate visual cortical organization.

Authors:  Marcello G P Rosa; Rowan Tweedale
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2005-04-29       Impact factor: 6.237

Review 6.  The future of mapping sensory cortex in primates: three of many remaining issues.

Authors:  Jon H Kaas
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2005-04-29       Impact factor: 6.237

Review 7.  Pulvinar contributions to the dorsal and ventral streams of visual processing in primates.

Authors:  Jon H Kaas; David C Lyon
Journal:  Brain Res Rev       Date:  2007-03-12

8.  Coding of stereoscopic depth information in visual areas V3 and V3A.

Authors:  Akiyuki Anzai; Syed A Chowdhury; Gregory C DeAngelis
Journal:  J Neurosci       Date:  2011-07-13       Impact factor: 6.167

9.  Behavioral detection of electrical microstimulation in different cortical visual areas.

Authors:  Dona K Murphey; John H R Maunsell
Journal:  Curr Biol       Date:  2007-04-26       Impact factor: 10.834

10.  Neural coding of 3D features of objects for hand action in the parietal cortex of the monkey.

Authors:  H Sakata; M Taira; M Kusunoki; A Murata; Y Tanaka; K Tsutsui
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1998-08-29       Impact factor: 6.237

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