Foveal flicker contrast sensitivity was measured for healthy adults at temporal frequencies from 2.5 to 50 Hz. The first experiment compared two-interval forced-choice (2IFC) and yes-no detection (Y-N) testing procedures for younger (19-33-year-old) and older (67-73-year-old) observers. The 2IFC technique resulted in higher absolute estimates of sensitivity. However, within a method, relative differences were similar. Therefore the two methods gave similar estimates of temporal contrast-sensitivity change with age. Experiment 2 compared 89 observers from 18 through 77 years of age to explore the effect of the time course of aging on flicker sensitivity. The 2IFC procedure was used, and retinal illuminance changes with age were controlled. Significant overall losses in contrast sensitivity were found for the 45-54, 55-64, and 65-77-year-old age groups. Overall sensitivities for the 35-44-year-old group were comparable with or (not significantly) higher than those for the 18-24- and 25-34-year-old groups. The results suggested that (1) foveal temporal contrast sensitivity does not decline until after 44 years, (2) losses after 44 years are in amplitude but not in temporal resolution of the visual response, and (3) the mean rate of loss is approximately 0.78 decilog per decade after 44 years. These results are consistent with the existence of three phases of development of temporal contrast sensitivity over the life span. The results also emphasize the importance of including healthy-eyed age-matched controls in studies of flicker sensitivity in visual dysfunctions that affect mainly older adults.

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Photopic temporal contrast sensitivity for healthy eyes of observers 65 years old and older is compared with retinal-illuminance-matched sensitivity of younger eyes. The older observers are significantly less sensitive for frequencies between 10 and 45 Hz. Although there is a slight shift to slower flicker rates in the mean contrast sensitivity function for older observers, this trend is not statistically significant, suggesting that there is relatively little loss of temporal resolving power of the visual system with healthy aging. These are preliminary results from an ongoing study of temporal contrast sensitivity in healthy aging eyes.

Studies of the numbers of retinal ganglion cells and lateral geniculate nucleus (LGN) neurons in primatessuggest that the numbers of both types of neurons may vary over a two-fold range from one individual to another. This raises the question of whether the numbers of ganglion cells and LGN neurons are related or vary independently from individual to individual. We used stereological procedures to obtain unbiased estimates of the numbers of both cell types in seven rhesus monkeys. We found no significant correlation (r s = -0.21) between the numbers of retinal and LGN cells in the same animals. In agreement with previous studies, the average ratio of the number of retinal ganglion cells that project to the LGN and the number of LGN cells was approximately 1:1. However, this ratio varied over a two-fold range, from 0.78:1 to 1.64:1, in individual animals. These results have important implications for understanding the mechanisms of retino-geniculate development and for understanding the connectional wiring between the retina and LGN.