Hostname: page-component-cd9895bd7-fscjk Total loading time: 0 Render date: 2024-12-26T00:33:13.944Z Has data issue: false hasContentIssue false
  • English
  • Français

Multi-microelectrode investigation of monkey striate cortex: Link between correlational and neuronal properties in the infragranular layers

Published online by Cambridge University Press:  02 June 2009

J. Krüger
J. Krüger
Affiliation:
Neurologische Universitätsklinik, Hansastrasse 9, D 7800 Freiburg, Federal Republic of Germany
Get access Rights & Permissions [Opens in a new window]

Abstract

Recordings were taken from infragranular layers of area 17 of anesthetized monkeys with an array of 30 microelectrodes matching about one hypercolumn. From intracortical spike-train correlations, the novel neuronal property “delay scale position” related to retino-cortical delays, was derived. Relationships were established to the degree of spike isolation and to classical response properties. Direction selectivity, spike rate, spike-isolation quality, delay scale, and color selectivity could be linked to an underlying factor upon which the latter variables depend in a fixed way. Neurons with similar factors were characterized by non-delayed correlations. The link was more strict in layer VI than in layer V, and it was related to the parvo/magnocellular subdivision of the visual system.

Keywords

CortexVisionMonkeyMultiple microelectrode
Type
Research Article
Information
Visual Neuroscience , Volume 5 , Issue 2 , August 1990 , pp. 135 - 142
Copyright
Copyright © Cambridge University Press 1990

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Aertsen, A.M.H.J. & Gerstein, G.L. (1985). Evaluation of neuronal connectivity: sensitivity of cross correlation. Brain Research 340, 341–354.CrossRefGoogle ScholarPubMed
Aiple, F. & Krüger, J. (1988). Neuronal synchrony in monkey striate cortex: interocular signal flow and dependency on spike rates. Experimental Brain Research 72, 141–149.CrossRefGoogle ScholarPubMed
Baker, J., Petersen, S.E., Newsome, W.T. & Allman, J.M. (1981). Visual-response properties of neurons in four extrastriate visual areas of the owl monkey (Aotus trivirgatus): a quantitative comparison of medial, dorsomedial, dorsolateral, and middle temporal areas. Journal of Neurophysiology 45, 397–416.CrossRefGoogle ScholarPubMed
Dixon, W.J., & Brown, M.B. (1979). Biomedical computer programs, P-series. Berkeley: University of California Press.Google Scholar
Finlay, B.L., Schiller, P.H. & Volman, S.F. (1976). Quantitative studies of single-cell properties in monkey striate cortex, IV: Corticotectal cells. Journal of Neurophysiology 39, 1352–1361.CrossRefGoogle ScholarPubMed
Fries, W. (1986). Distribution of Meynert cells in primate striate cortex. Naturwiss. 73, 557–558.CrossRefGoogle ScholarPubMed
Gouras, P. (1968). Identification of cone mechanisms in monkey ganglion cells. Journal of Physiology, (London) 199, 533–547.CrossRefGoogle ScholarPubMed
Grover, F.S. & Bucuhwald, J.S. (1970). Correlations of cell size with amplitude of background fast activity in specific brain nuclei. Journal of Neurophysiology 33, 160–171.CrossRefGoogle ScholarPubMed
Hammond, P. & MacKay, D.M. (1977). Differential responsiveness of simple and complex cells in cat striate cortex to visual texture. Experimental Brain Research 30, 275–296.Google ScholarPubMed
Hubel, D.H. & Wiesel, T.N. (1968). Receptive fields and functional architecture of monkey striate cortex. Journal of Physiology (London) 195, 215–243.CrossRefGoogle ScholarPubMed
Krüger, J. (1977). Stimulus-dependent colour specificity of monkey lateral geniculate neurones. Experimental Brain Research 30, 297–311.Google ScholarPubMed
Krüger, J. & Aiple, F. (1988). Multi-microelectrode investigation of monkey striate cortex: spike-train correlations in the infragranular layers. Journal of Neurophysiology 60, 798–828.CrossRefGoogle Scholar
Krüger, J. & Aiple, F. (1989). The connectivity underlying the orientation selectivity in monkey striate cortex. Brain Research 477, 57–65.CrossRefGoogle ScholarPubMed
Krüger, J. & Bach, M. (1982). Independent systems of orientation columns in upper and lower layers of monkey visual cortex. Neuroscience Letters 31, 225–230.CrossRefGoogle ScholarPubMed
Livingstone, M.S. & Hubel, D.H. (1984). Anatomy and physiology of a color system in the primate visual cortex. Journal of Neuroscience 4, 309–356.CrossRefGoogle ScholarPubMed
Lund, J.S. & Boothe, R.G. (1975). Interlaminar connections and pyramidal neuron organization in the visual cortex, area 17, of the macaque monkey. Journal of Comparative Neurology 159, 305–334.CrossRefGoogle Scholar
Lund, J.S., Lund, R.D., Hendrickson, A.E., Bunt, A.H., & Fuchs, A.F. (1975). The origin of efferent pathways from the primary visual cortex, area 17, of the macaque monkey as shown by retrograde transport of horseradish peroxidase. Journal of Comparative Neurology 164, 287–304.CrossRefGoogle ScholarPubMed
Maunsell, J.H.R. & Van Essen, D.C. (1983). Functional properties of neurons in middle temporal visual area of the macaque monkey, I: Selectivity for stimulus direction, speed, and orientation. Journal of Neurophysiology 49, 1127–1147.CrossRefGoogle ScholarPubMed
Schiller, P.H. & Malpeli, J.G. (1978). Functional specificity of lateral geniculate nucleus laminae of the rhesus monkey. Journal of Neurophysiology 41, 788–797.CrossRefGoogle ScholarPubMed
Spatz, W.B. (1975). An efferent connection of the solitary cells of Meynert. A study with horseradish peroxidase in the marmoset (Callithrix). Brain Research 92, 450–455.CrossRefGoogle Scholar
Zeki, S.M. (1974). Functional organization of a visual area in the posterior bank of the superior temporal sulcus of the rhesus monkey. Journal of Physiology (London) 236, 549–573.CrossRefGoogle ScholarPubMed