Biological Cybernetics

, Volume 57, Issue 4–5, pp 331–340 | Cite as

The construction of a simultaneous functional order in nervous systems

III. The influence of environmental constraints on the resulting functional order
  • A. Toet
  • J. Blom
  • J. J. Koenderink
Article

Abstract

In a previous paper (Part I) we introduced a model that constructs a simultaneous functional order in a set of neuronal elements by monitoring the coincidences in their signal activities (the so-called coincidence-model). The simultaneous signal activity in a neural net will be constrained both by its physical restrictions and by environmental constraints. In this paper we present the results of simulation experiments that were performed to study the influence of environmental constraits on the resulting functional order in a set of neural elements corresponding to a onedimensional detector array. We show that the coincidence-model produces a functional order that encodes the physical constraints of the environment. Moreover, we demonstrate that the signal activity in the neural net (the “perceptions”) can be related to events in the outer world. We provide some examples to demonstrate that our model may prove useful to gain insight into certain developmental disorders.

Keywords

Nervous System Simulation Experiment Signal Activity Detector Array Developmental Disorder 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Bedi KS (1986) Nutrition, environment and brain development. Sci Prog 70:555–570Google Scholar
  2. Blakemore C, Cooper GF (1970) Development of the brain depends on the visual environment. Nature 228:477–478Google Scholar
  3. Cowan WM, Fawcett JW, O'Leary DDM, Stanfield BB (1984) Regressive events in neurogenesis. Science 225:1258–1265Google Scholar
  4. Hess RF (1982) Developmental sensory impairment: amblyopia or tarachopia? Hum Neurobiol 1:17–29Google Scholar
  5. Hirsch HVB, Leventhal AG (1978) Functional modification of the developing visual system. In: Jacobson M (ed) Handbook of sensory physiology IX. Springer, Berlin Heidelberg New York, pp 279–335Google Scholar
  6. Hirsch HVB, Spinelli DN (1970) Visual experience modifies distribution of horizontally and vertically oriented receptive fields in cats. Science 168:869–871Google Scholar
  7. Hubel DH, Wiesel TN (1970) The period of susceptibility to the physiological effects of unilateral eye closure in kittens. J Physiol (Lond) 206:419–436Google Scholar
  8. Hubel DH, Wiesel TN (1974) Ordered arrangement of orientation columns in monkeys lacking visual experience. J Comp Neurol 158:307–318Google Scholar
  9. Ikeda H (1980) Visual acuity, its development and amblyopia. J R Soc Med 73:546–555Google Scholar
  10. Ikeda H, Wright MJ (1974) Is amblyopia due to inappropriate stimulation of the “sustained” pathway during development? Br J Ophthal 58:165–175Google Scholar
  11. Jeffery G (1985) Retinotopic order appears before ocular separation in developing visual pathways. Nature 313:575–576Google Scholar
  12. Kandel ER (1985a) Early experience, critical periods, and developmental fine tuning of brain architecture. In: Kandel ER, Schwartz JH (eds) Principles of neural science, 2nd ed. Elsevier, New York Amsterdam OxfordGoogle Scholar
  13. Kandel ER (1985b) Cellular mechanisms of learning and the biological basis of individuality. In: Kandel ER, Schwartz JH (eds) Principles of neural science, 2nd edn. Elsevier, New York Amsterdam OxfordGoogle Scholar
  14. Mitchell DE, Freeman RD, Millodot M, Haegerstrom G (1973) Meridional amblyopia: evidence for modification of the human visual system by early visual experience. Vision Res 13:535–558Google Scholar
  15. Moyshon JA, Sluyters RC van (1982) Visual neural development. Annu Rev Psychol 32:477–522Google Scholar
  16. Paton JA, Nottebohm FN (1984) Neurons generated in the adult brain are recruited into functional circuits. Science 225:1046–1048Google Scholar
  17. Pettigrew JD, Freeman RD (1973) Visual experience without lines: effect on developing cortical neurons. Science 182:599–601Google Scholar
  18. Stryker MP, Sherk H, Leventhal AG, Hirsch HVB (1978) Physiological consequences for the cat's visual cortex of effectively restricting early visual experience with oriented contours. J Neurophysiol 41:896–909Google Scholar
  19. Toet A, Blom J, Koenderink JJ (1987a) The construction of a simultaneous functional order in nervous systems. I. Relevance of signal covariances and signal coincidences in the construction of a functional order. Biol Cybern 57:115–125Google Scholar
  20. Toet A, Blom J, Koenderink JJ (1987b) The construction of a simultaneous functional order in nervous systems. II. Computing geometrical structures. Biol Cybern 57:127–136Google Scholar
  21. Wiesel TN (1982) Postnatal developments of the visual cortex and the influence of environment. Nature 299:583–591Google Scholar

Copyright information

© Springer-Verlag 1987

Authors and Affiliations

  • A. Toet
    • 1
  • J. Blom
    • 1
  • J. J. Koenderink
    • 1
  1. 1.Department of Medical and Physiological PhysicsUniversity of UtrechtUtrechtThe Netherlands

Personalised recommendations