Literature DB >> 7658377

Contributions of human long-wave and middle-wave cones to motion detection.

C F Stromeyer1, R E Kronauer, A Ryu, A Chaparro, R T Eskew.   

Abstract

1. It has been suggested that motion may be best detected by the luminance mechanism. If this is the most sensitive mechanism, motion thresholds may be used to isolate the luminance mechanism and study its properties. 2. A moving (1 cycle deg-1), vertical, heterochromatic (red-plus-green), foveal grating was presented on a bright yellow (577 nm wavelength) field. Detection and motion (direction identification: left versus right) thresholds were measured for different amplitude ratios of the red and green components spatially summed in phase or in antiphase. Threshold contours plotted in cone-contrast co-ordinates (L',M') for the long-wave (L) and middle-wave (M) cones, revealed two motion mechanisms: a luminance mechanism that responds to a weighted sum of L and M contrasts, and a spectrally opponent mechanism that responds to a weighted difference. 3. Detection and motion thresholds, measured at 1-4 Hz, were identical for luminance gratings, having equal cone contrasts, L' and M', of the same sign. For chromatic gratings, with L' and M' of opposite sign, motion thresholds were higher than detection thresholds. A red-green hue mechanism may mediate chromatic detection, and a separate spectrally opponent motion mechanism may mediate motion. 4. The red-green hue mechanism was assessed from 1 to 15 Hz with an explicit hue criterion. The detection contour had a constant slope of one, implying equal L' and M' contributions of opposite sign. For motion identification, L' and M' contributed equally at 1 Hz, but the M' contribution was attenuated at higher velocities. 5. The cone-contrast metric provides a physiologically relevant comparison of sensitivities of the two motion mechanisms. At 1 Hz, the spectrally opponent motion mechanism is approximately 4 times more sensitive than the luminance mechanism. As temporal frequency is increased, the relative sensitivities change so that the luminance mechanism is more sensitive above 9 Hz. 6. The less sensitive motion mechanism was isolated with a quadrature phase protocol, using a pair of heterochromatic red-plus-green gratings, counterphase flickering in spatial and temporal quadrature phase with respect to each other. One grating was set slightly suprathreshold and oriented in cone contrast (L',M') so as to potentiate a single motion mechanism, the sensitivity of which was probed with the second grating, which was varied in (L',M'). This allowed us to measure the motion detection contour of the less sensitive luminance mechanism at low velocities.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1995        PMID: 7658377      PMCID: PMC1157986          DOI: 10.1113/jphysiol.1995.sp020726

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


  42 in total

1.  Spectral sensitivity of the foveal cone photopigments between 400 and 500 nm.

Authors:  V C Smith; J Pokorny
Journal:  Vision Res       Date:  1975-02       Impact factor: 1.886

2.  Peripheral chromatic sensitivity for flashes: a post-receptoral red-green asymmetry.

Authors:  C F Stromeyer; J Lee; R T Eskew
Journal:  Vision Res       Date:  1992-10       Impact factor: 1.886

3.  Interactions between colour and luminance contrast in the perception of motion.

Authors:  K T Mullen; J C Boulton
Journal:  Ophthalmic Physiol Opt       Date:  1992-04       Impact factor: 3.117

4.  Spatial and chromatic interactions in the lateral geniculate body of the rhesus monkey.

Authors:  T N Wiesel; D H Hubel
Journal:  J Neurophysiol       Date:  1966-11       Impact factor: 2.714

5.  Functional segregation of color and motion perception examined in motion nulling.

Authors:  E J Chichilnisky; D Heeger; B A Wandell
Journal:  Vision Res       Date:  1993-10       Impact factor: 1.886

6.  Detecting and discriminating the direction of motion of luminance and colour gratings.

Authors:  A M Derrington; G B Henning
Journal:  Vision Res       Date:  1993 Mar-Apr       Impact factor: 1.886

7.  Motion at isoluminance: discrimination/detection ratios and the summation of luminance and chromatic signals.

Authors:  J Palmer; L A Mobley; D Y Teller
Journal:  J Opt Soc Am A       Date:  1993-06       Impact factor: 2.129

8.  Contrast adaptation dissociates different measures of luminous efficiency.

Authors:  M A Webster; J D Mollon
Journal:  J Opt Soc Am A       Date:  1993-06       Impact factor: 2.129

9.  Chromatic properties of neurons in macaque MT.

Authors:  K R Gegenfurtner; D C Kiper; J M Beusmans; M Carandini; Q Zaidi; J A Movshon
Journal:  Vis Neurosci       Date:  1994 May-Jun       Impact factor: 3.241

10.  Detection and discrimination of moving stimuli: the effects of color, luminance, and eccentricity.

Authors:  A B Metha; A J Vingrys; D R Badcock
Journal:  J Opt Soc Am A Opt Image Sci Vis       Date:  1994-06       Impact factor: 2.129

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  12 in total

Review 1.  More than one way to see it move?

Authors:  T D Albright
Journal:  Proc Natl Acad Sci U S A       Date:  1999-07-06       Impact factor: 11.205

2.  The contribution of color to motion processing in Macaque middle temporal area.

Authors:  A Thiele; K R Dobkins; T D Albright
Journal:  J Neurosci       Date:  1999-08-01       Impact factor: 6.167

3.  Colour adaptation modifies the temporal properties of the long- and middle-wave cone signals in the human luminance mechanism.

Authors:  C F Stromeyer; P D Gowdy; A Chaparro; S Kladakis; J D Willen; R E Kronauer
Journal:  J Physiol       Date:  2000-07-01       Impact factor: 5.182

4.  A linear chromatic mechanism drives the pupillary response.

Authors:  S Tsujimura; J S Wolffsohn; B Gilmartin
Journal:  Proc Biol Sci       Date:  2001-11-07       Impact factor: 5.349

5.  Colour and luminance interactions in the visual perception of motion.

Authors:  Alexandra Willis; Stephen J Anderson
Journal:  Proc Biol Sci       Date:  2002-05-22       Impact factor: 5.349

6.  Spectrally opponent inputs to the human luminance pathway: slow +L and -M cone inputs revealed by low to moderate long-wavelength adaptation.

Authors:  Andrew Stockman; Daniel J Plummer
Journal:  J Physiol       Date:  2005-04-28       Impact factor: 5.182

7.  Spectrally opponent inputs to the human luminance pathway: slow +M and -L cone inputs revealed by intense long-wavelength adaptation.

Authors:  Andrew Stockman; Daniel J Plummer; Ethan D Montag
Journal:  J Physiol       Date:  2005-04-28       Impact factor: 5.182

8.  Colour adaptation modifies the long-wave versus middle-wave cone weights and temporal phases in human luminance (but not red-green) mechanism.

Authors:  C F Stromeyer; A Chaparro; A S Tolias; R E Kronauer
Journal:  J Physiol       Date:  1997-02-15       Impact factor: 5.182

9.  Effect of cone spectral topography on chromatic detection sensitivity.

Authors:  Alexandra Neitz; Xiaoyun Jiang; James A Kuchenbecker; Niklas Domdei; Wolf Harmening; Hongyi Yan; Jihyun Yeonan-Kim; Sara S Patterson; Maureen Neitz; Jay Neitz; Daniel R Coates; Ramkumar Sabesan
Journal:  J Opt Soc Am A Opt Image Sci Vis       Date:  2020-04-01       Impact factor: 2.129

10.  Separate colour-opponent mechanisms underlie the detection and discrimination of moving chromatic targets.

Authors:  A Willis; S J Anderson
Journal:  Proc Biol Sci       Date:  1998-12-22       Impact factor: 5.349

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