Literature DB >> 5498455

The size of rod signals.

M Alpern, W A Rushton, S Torii.   

Abstract

1. This investigation is based upon Alpern's (1965) contrast flash observations. The threshold for the test flash lambda (Fig. 2a) is raised if a second flash varphi falls on the annular surround. Moreover, if lambda excites rods at threshold, it is only the rods in the surround that contribute to the threshold rise.2. The possibility that the rise in lambda threshold might be due to light physically scattered from surround to centre we exclude by several different experiments. We conclude (Fig. 1b) that the varphi flash sets up a nerve signal N which is conducted to some place C where it inhibits the signal from the centre.3. If the luminous surround, instead of being a full circle (Fig. 2a) consists only of the sectors shown black in Fig. 2b, that occupy 1/m of the surround area, it is found (in the physiological range) that the light/area on those sectors must be m times as great to produce the same threshold rise at centre, i.e. the total surround illumination must remain the same.4. This result would obviously follow if N, the inhibitory nerve signal, were proportional to the total surround illumination. We have established the converse; the signal must be proportional to the quantum catch.5. Light can be increased indefinitely, nerve signals cannot. When varphi increases sufficiently, N saturates in the same way that S-potentials and receptor potentials saturate, namely according to N = varphi/(varphi + sigma) where sigma, the semi-saturation constant is about 200 td sec, or 800 quanta absorbed per rod per flash.6. Thus the nerve signal N is proportional to the quantum catch over 4 log units in the physiological range, namely from 1 quantum per 100 rods to 100 quanta per rod per flash. Above this for another 2 log units N continues to increase, but now more slowly, after the manner of S-potentials and receptor potentials.

Mesh:

Year:  1970        PMID: 5498455      PMCID: PMC1348595          DOI: 10.1113/jphysiol.1970.sp009006

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


  10 in total

1.  ROD-CONE INDEPENDENCE IN THE AFTER-FLASH EFFECT.

Authors:  M ALPERN
Journal:  J Physiol       Date:  1965-02       Impact factor: 5.182

2.  THE SPECIFICITY OF THE CONE INTERACTION IN THE AFTER-FLASH EFFECT.

Authors:  M ALPERN; W A RUSHTON
Journal:  J Physiol       Date:  1965-02       Impact factor: 5.182

3.  THE SENSITIVITY OF RODS UNDER ILLUMINATION.

Authors:  W A RUSHTON
Journal:  J Physiol       Date:  1965-05       Impact factor: 5.182

4.  The absolute sensitivity and functional stability of the human eye.

Authors:  E J DENTON; M H PIRENNE
Journal:  J Physiol       Date:  1954-03-29       Impact factor: 5.182

5.  The nature of rise in threshold produced by contrast-flashes.

Authors:  M Alpern; W A Rushton
Journal:  J Physiol       Date:  1967-04       Impact factor: 5.182

6.  Computer assisted analysis of S-potentials.

Authors:  K I Naka
Journal:  Biophys J       Date:  1969-06       Impact factor: 4.033

7.  Glare: its measurement by cone thresholds and by the bleaching of cone pigments.

Authors:  W A Rushton; R W Gubisch
Journal:  J Opt Soc Am       Date:  1966-01

8.  The generation and spread of S-potentials in fish (Cyprinidae).

Authors:  K I Naka; W A Rushton
Journal:  J Physiol       Date:  1967-09       Impact factor: 5.182

9.  Organization of the retina of the mudpuppy, Necturus maculosus. II. Intracellular recording.

Authors:  F S Werblin; J E Dowling
Journal:  J Neurophysiol       Date:  1969-05       Impact factor: 2.714

10.  S-potentials from luminosity units in the retina of fish (Cyprinidae).

Authors:  K I Naka; W A Rushton
Journal:  J Physiol       Date:  1966-08       Impact factor: 5.182

  10 in total
  19 in total

1.  On the analysis of nerve signals deduced from metacontrast experiments with human observers.

Authors:  B A Wandell
Journal:  J Physiol       Date:  1976-12       Impact factor: 5.182

2.  Rod-rod interaction in the retina of the turtle.

Authors:  E A Schwartz
Journal:  J Physiol       Date:  1975-04       Impact factor: 5.182

3.  Rod-cone interaction in light adaptation.

Authors:  M Latch; P Lennie
Journal:  J Physiol       Date:  1977-08       Impact factor: 5.182

4.  Interpreting trans-retinal recordings of spectral sensitivity.

Authors:  T H Goldsmith
Journal:  J Comp Physiol A       Date:  1986-10       Impact factor: 1.836

5.  Responses of crayfish photoreceptor cells following intense light adaptation.

Authors:  D R Cummins; T H Goldsmith
Journal:  J Comp Physiol A       Date:  1986-01       Impact factor: 1.836

Review 6.  Pigments and signals in colour vision.

Authors:  W A Rushton
Journal:  J Physiol       Date:  1972-02       Impact factor: 5.182

7.  The effect of selective medullary coagulation on the cardiovascular response to intravenous infusion of angiotensin in the rabbit.

Authors:  M D Joy; P J Lewis
Journal:  J Physiol       Date:  1971-10       Impact factor: 5.182

Review 8.  Toward a general theory of visual adaptation.

Authors:  R M Glantz
Journal:  Doc Ophthalmol       Date:  1971-09-12       Impact factor: 2.379

9.  Background configuration and rod threshold.

Authors:  P Lennie; D I MacLeod
Journal:  J Physiol       Date:  1973-08       Impact factor: 5.182

10.  On the retinal basis of visual adaptation.

Authors:  K N Leibovic
Journal:  Kybernetik       Date:  1971-09
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