A B S T R A C TExtracellular microelectrode recordings were made from ganglion cells of the intact, in situ eyes of adult common domestic cats. Three different photopic systems, with peak spectral sensitivities at 450, 500, and 556 nm, were observed. All ganglion cells received input from a cone system with a peak spectral sensitivity of 556 nm. The blue-sensitive cone system was observed in about one-half of the ganglion cells studied. In each case the 450-nm cone system contributed to only one functional type of response, either ON or OFF, in the same cell. The other two photopic systems most often contributed to both the ON and OFF responses of an individual ganglion cell. In four cases the 450-nm cone system mediated responses that were opponent to those of the other two photopic systems. The third photopic mechanism has a peak spectral sensitivity at 500 nm and contributed to most receptive field surrounds and many receptive field centers. It is distinguished from the rod system by the occurrence of a break in both dark-adaptation curves and increment-sensitivity curves. No apparent differences in receptive field cone contributions between brisk-sustained and brisk-transient cells were seen.
INTRODUCTIONThe early electrophysiological analysis of the cat retina by Granit (1943 and1948) and his co-workers suggested that there is more than one cone type. Under scotopic conditions, they observed good agreement between the spectral-sensitivity curves of many cat retinal ganglion cells and visual purple data. However, with other ganglion cells, especially under photopic conditions, the curves showed "humps," often at the blue end of the spectrum, but frequently also at the red end. By direct and indirect means they sought to separate the very broad and irregular dominator curves into narrow modulator curves with single peaks. They found so many maximums that the spectral sensitivities of the primary photochemical substances were not clear. They proposed that the various phenomena could be grouped into three regions of the spectrum, and that there were three chromatically distinct cone populations.Until recently, attempts to demonstrate by behavioral tests the existence of wavelength discrimination in the cat have led to negative results or, at most, to positive results that were very difficult to obtain. The work of Gunter (1954) and of Meyer et al. (1954) failed to show any wavelength discrimination in the cat. Sechzer and Brown (1964) succeeded in training cats to distinguish between broad-band green and red lights. Other behavioral studies confirmed that the cat can be trained, although with great difficulty, to distinguish long from short wavelengths (see, e.g., Mellow and Peterson I1964] and Meyer and Anderson [1965]). Daw and Pearlman (1969) examined the wavelength sensitivity of the cat in extracellular recordings from single units in the lateral geniculate and in the optic tract. At background levels exceeding rod saturation according to their tests, they found evidence for only one cone mechanism (556-...