Path: utzoo!utgpu!news-server.csri.toronto.edu!rpi!bu.edu!snorkelwacker.mit.edu!stanford.edu!medisg.stanford.edu!cmgm!vangeldr From: vangeldr@cmgm.Stanford.EDU (Russ Van Gelder) Newsgroups: sci.bio Subject: Re: Primary colors in human color vision Summary: A little more information Message-ID: <1991Mar24.002117.24100@medisg.Stanford.EDU> Date: 24 Mar 91 00:21:17 GMT References: <00945FE5.1F9B5480@aclcb.purdue.edu> <1991Mar23.193006.22992@pinhead.pegasus.com> Sender: news@medisg.Stanford.EDU Organization: Stanford Center for Molecular and Genetic Medicine - CMGM Lines: 40 A little more information on trichromacy. The original experiments which indicated that there are three photoreceptors came from experiments where subjects were asked to match any given hue with combinations of 2, 3, or 4 single colors; 3 turned out to be sufficient when the colors were red, green, and blue (RGB). Further work showed that color vision is mediated by the cones of the retina, which are concentrated in the region of highest visual acuity, the fovea. The surrounding areas are primarily populated by the more sensitive rods, which are used in night vision. This distribution explains why astronomers often peer at the stars using their peripheral vision; looking dead-on at a star dims its appearance because of the lower efficiency of capture and signal transduction of the cones in the fovea. The cone pigments themselves are fascinating. Like the rods' rhodopsin, the cone pigments are made up of a vitamin A-derived molecule, retinal, and a specific protein, opsin. There are three opsins, one for each color. One cone cell makes only one kind of opsin; how this level of differentiation is established is a great open question. Equally intriguing is understanding how the cone pigments "tune" the retinal; it is the same photoisomerization of 11-cis retinal to all trans which is the essential act of photoreception in all three cone rhodopsins. Something about the particular side-chains in the vicinity of the retinal must influence the absorption spectrum of the molecule; Jeremy Nathans (who worked out much of the molecular biology and genetics of human color vision) has been making site-directed mutants of the color opsins and thinks that the relative localization of charge on the retinal is responsible for its spectral absorbance. Higher order effects occur at the levels of center-surround interactions in bipolar and ganglion cells, and cortical processing; a number of optical illusions exists which show that the same spectral distribution is sensed as different color depending on its surround-field. No good algorithm yet exists for predicting how a particular spectral field will appear, which is to say that even the psychophysics of higher order visual perception are not yet well understood. Russ