Opponent process


Opponent colors based on the NCS experiment. Deuteranopes see little difference between the two colors in the central column.
Diagram of the opponent process
Log-log plot of spatial contrast sensitivity functions for luminance and chromatic contrast

The opponent process is a color theory that states that the human visual system interprets information about color by processing signals from cone cells and rod cells in an antagonistic manner. There is some overlap in the wavelengths of light to which the three types of cones (L for long-wave, M for medium-wave, and S for short-wave light) respond, so it is more efficient for the visual system to record differences between the responses of cones, rather than each type of cone's individual response. The opponent color theory suggests that there are three opponent channels the cone photoreceptors are linked together to form three opposing color pairs: red versus green, blue versus yellow, and black versus white (the last type is achromatic and detects light-dark variation, or luminance).[1] It was first proposed in 1892 by the German physiologist Ewald Hering.

When people stare at a bright color for too long, for example, red, and look away at a white field they will perceive a green color. Activation of one member of the pair inhibits activity in the other. This theory also helps to explain some types of color vision deficiency. For example, people with dichromatic deficiencies must match a test field using only two primaries. Depending on the deficiency they will confuse either red and green or blue and yellow. The opponent-process theory explains color vision as a result of the way in which photoreceptors are interconnected neurally. The opponent-process theory applies to different levels of the nervous system. Once the neural system passes beyond the retina to the brain, the nature of the cell changes and the cell responds in an opponent fashion. For example, the green and red photoreceptor might each send a signal to the blue-red opponent cell farther along with the system. Responses to one color of an opponent channel are antagonistic to those to the other color. That is, opposite opponent colors are never perceived together – there is no "greenish red" or "yellowish blue".

While the trichromatic theory defines the way the retina of the eye allows the visual system to detect color with three types of cones, the opponent process theory accounts for mechanisms that receive and process information from cones. Though the trichromatic and opponent processes theories were initially thought to be at odds, it later came to be understood that the mechanisms responsible for the opponent process receive signals from the three types of cones and process them at a more complex level.[2]

Besides the cones, which detect light entering the eye, the biological basis of the opponent theory involves two other types of cells: bipolar cells, and ganglion cells. Information from the cones is passed to the bipolar cells in the retina, which may be the cells in the opponent process that transform the information from cones. The information is then passed to ganglion cells, of which there are two major classes: magnocellular, or large-cell layers, and parvocellular, or small-cell layers. Parvocellular cells, or P cells, handle the majority of information about color and fall into two groups: one that processes information about differences between the firing of L and M cones, and one that processes differences between S cones and a combined signal from both L and M cones. The first subtype of cells is responsible for processing red–green differences, and the second process blue–yellow differences. P cells also transmit information about the intensity of light (how much of it there is) due to their receptive fields.[citation needed]


Johann Wolfgang von Goethe first studied the physiological effect of opposed colors in his Theory of Colours in 1810.[3] Goethe arranged his color wheel symmetrically "for the colours diametrically opposed to each other in this diagram are those which reciprocally evoke each other in the eye. Thus, yellow demands purple; orange, blue; red, green; and vice versa: Thus again all intermediate gradations reciprocally evoke each other."[4][5]

Ewald Hering proposed opponent color theory in 1892.[6] He thought that the colors red, yellow, green, and blue are special in that any other color can be described as a mix of them, and that they exist in opposite pairs. That is, either red or green is perceived and never greenish-red: Even though yellow is a mixture of red and green in the RGB color theory, the eye does not perceive it as such. In 1957, Leo Hurvich and Dorothea Jameson provided quantitative data for Hering's color-opponent theory. Their method was called hue cancellation. Hue cancellation experiments start with a color (e.g. yellow) and attempt to determine how much of the opponent color (e.g. blue) of one of the starting color's components must be added to eliminate any hint of that component from the starting color.[7][8] In 1959, Gunnar Svaetichin and MacNichol[9] recorded from the retina of fish and reported of three distinct types of cells: one responded with hyperpolarization to all light stimuli regardless of wavelength and was termed a luminosity cell. A second cell responded with hyperpolarization at short wavelengths and with depolarization at mid-to-long wavelengths. This was termed a chromaticity cell. A third cell, also a chromaticity cell, responded with hyperpolarization at fairly short wave- lengths, peaking about 490 nm, and with depolarization at wavelengths longer than about 610 nm. Gunnar Svaetichin and MacNichol called the chromaticity cells Yellow- Blue and Red-Green opponent color cells. Similar chromatically or spectrally opposed cells, often incorporating spatial-opponency (e.g. red "on" center and green "off" surround), were found in the vertebrate retina and lateral geniculate nucleus (LGN) through the 1950s and 1960s by De Valois et al.,[10] Wiesel and Hubel,[11] and others.[12][13][14][15] After Gunnar Svaetichin's lead, the cells were widely called opponent colour cells, Red-Green and Yellow-Blue. Over the next three decades, spectrally opposed cells continued to be reported in primate retina and LGN.[16][17][18][19] A variety of terms are used in the literature to describe these cells, including chromatically opposed or -opponent, spectrally opposed or -opponent, opponent colour, colour opponent, opponent response, and simply, opponent cell.

The opponent color theory can be applied to computer vision and implemented as the Gaussian color model[20] and the natural-vision-processing model.[21][22][23]

Others have applied the idea of opposing stimulations beyond visual systems, described in the article on opponent-process theory. In 1967, Rod Grigg extended the concept to reflect a wide range of opponent processes in biological systems.[24] In 1970, Solomon and Corbit expanded Hurvich and Jameson's general neurological opponent process model to explain emotion, drug addiction, and work motivation.[25][26]

Criticism and the complementary color cells

Much controversy exists over whether opponent-processing theory is the best way to explain color vision. A few experiments have been conducted involving image stabilization (where one experiences border loss) that produced results that suggest participants have seen “impossible” colors, or color combinations humans should not be able to see under the opponent-processing theory. However, many criticize that this result may just be illusionary experiences. Critics and researchers have instead started to turn to explain color vision through references to retinal mechanisms, rather than opponent processing, which happens in the brain's visual cortex.

As recordings from single cell accumulated, it became clear to many physiologists and psychophysicists that opponent colors did not satisfactorily account for single cell spectrally opposed responses. For instance, Jameson and D’Andrade[27] analyzed opponent-colors theory and found the unique hues did not match the spectrally opposed responses. De Valois himself[28] summed it up: “Although we, like others, were most impressed with finding opponent cells, in accord with Hering’s suggestions, when the Zeitgeist at the time was strongly opposed to the notion, the earliest recordings revealed a discrepancy between the Hering-Hurvich-Jameson opponent perceptual channels and the response characteristics of opponent cells in the macaque lateral geniculate nucleus.” Valberg[29] recalls that “it became common among neurophysiologists to use colour terms when referring to opponent cells as in the notations ‘red-ON cells’, ‘green-OFF cells’ .... In the debate .... some psychophysicists were happy to see what they believed to be opponency confirmed at an objective, physiological level. Consequently, little hesitation was shown in relating the unique and polar color pairs directly to cone opponency. Despite evidence to the contrary .... textbooks have, up to this day, repeated the misconception of relating unique hue perception directly to peripheral cone opponent processes. The analogy with Hering's hypothesis has been carried even further so as to imply that each color in the opponent pair of unique colors could be identified with either excitation or inhibition of one and the same type of opponent cell.” Webster et al.[30] and Wuerger et al.[31] have conclusively re-affirmed that single cell spectrally opposed responses do not align with unique-hue opponent colours.

More recent experiments show that the relationship between the responses of single "color-opponent" cells and perceptual color opponency is even more complex than supposed. Experiments by Zeki et al.,[32] using the Land Color Mondrian, have shown that when normal observers view, for example, a green surface which is part of a multi-colored scene and which reflects more green than red light it looks green and its after-image is magenta. But when the same green surface reflects more red than green light, it still looks green (because of the operation of color constancy mechanisms) and its after image is still perceived as magenta. This is true also of other colors and may be summarised by saying that, just as surfaces retain their color categories in spite of wide-ranging fluctuations in the wavelength-energy composition of the light reflected from them, the color of the after-image produced by viewing surfaces also retains its color category and is therefore also independent of the wavelength-energy composition of the light reflected from the patch being viewed. There is, in other words, a constancy to the colors of after images. This serves to emphasise further the need to search more deeply into the relationship between the responses of single opponent cells and perceptual color opponency on the one hand and the need for a better understanding of whether physiological opponent processes generate perceptual opponent colors or whether the latter are generated after colors are generated.

In 2013, Pridmore[33] argued that most Red-Green cells reported in the literature in fact code the Red-Cyan colors. Thus, the cells are coding complementary colors instead of opponent colors. Pridmore reported also of Green-Magenta cells in the retina and V1. He thus argued that the Red-Green and Blue-Yellow cells should be instead called "Green-magenta", "Red-cyan" and "Blue-yellow" complementary cells. An example of the complementary process can be experienced by staring at a red (or green) square for forty seconds, and then immediately looking at a white sheet of paper. The observer then perceives a cyan (or magenta) square on the blank sheet. This complementary color afterimage is more easily explained by the trichromatic color theory than the traditional RYB color theory; in the opponent-process theory, fatigue of pathways promoting red produce the illusion of a cyan square.[34]

Combinations of opponent colors

See also


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Further reading

  • Baccus SA (2007). "Timing and computation in inner retinal circuitry". Annual Review of Physiology. 69: 271–90. doi:10.1146/annurev.physiol.69.120205.124451. PMID 17059359.
  • Masland RH (August 2001). "Neuronal diversity in the retina". Current Opinion in Neurobiology. 11 (4): 431–6. doi:10.1016/S0959-4388(00)00230-0. PMID 11502388. S2CID 42917038.
  • Masland RH (September 2001). "The fundamental plan of the retina". Nature Neuroscience. 4 (9): 877–86. doi:10.1038/nn0901-877. PMID 11528418. S2CID 205429773.
  • Sowden PT, Schyns PG (December 2006). "Channel surfing in the visual brain" (PDF). Trends in Cognitive Sciences. 10 (12): 538–45. doi:10.1016/j.tics.2006.10.007. PMID 17071128. S2CID 6941223.
  • Wässle H (October 2004). "Parallel processing in the mammalian retina". Nature Reviews. Neuroscience. 5 (10): 747–57. doi:10.1038/nrn1497. PMID 15378035. S2CID 10518721.
  • Manzotti, R (2017). "A Perception-Based Model of Complementary Afterimages". SAGE Open. 7 (1). doi:10.1177/2158244016682478.
  • Yurtoğlu N (2018). "History Studies International Journal of History" (PDF). 10 (7): 241–264. doi:10.9737/hist.2018.658. {{cite journal}}: Cite journal requires |journal= (help)
  • Brogaard B, Gatzia DE (2016). "Cortical Color and the Cognitive Sciences". Topics in Cognitive Science. 9 (1): 135–150. doi:10.1111/tops.12241. PMID 28000986.