Neural undersampling of the retinal image limits the range of spatial frequencies that can be represented veridically by the array of retinal ganglion cells conveying visual information from eye to brain. Our goal was to demarcate the neural bandwidth and local anisotropy of veridical perception, unencumbered by optical imperfections of the eye, and to test competing hypotheses that might account for the results. Using monochromatic interference fringes to stimulate the retina with high-contrast sinusoidal gratings, we measured sampling-limited visual resolution along eight meridians from 0° to 50° of eccentricity. The resulting isoacuity contour maps revealed all of the expected features of the human array of retinal ganglion cells. Contours in the radial fringe maps are elongated horizontally, revealing the functional equivalent of the anatomical visual streak, and are extended into nasal retina and superior retina, indicating higher resolution along those meridians. Contours are larger in diameter for radial gratings compared to tangential or oblique gratings, indicating local anisotropy with highest bandwidth for radially oriented gratings. Comparison of these results to anatomical predictions indicates acuity is proportional to the sampling density of retinal ganglion cells everywhere in the retina. These results support the long-standing hypothesis that “pixel density” of the discrete neural image carried by the human optic nerve limits the spatial bandwidth of veridical perception at all retinal locations.

The causal predominance of performance affecting later cohesiveness that has been shown in previous studies was examined by means of a series of statistical analyses designed to assess influence in a longitudinal panel design. Male students (N = 44) participating in a basketball league were administered cohesiveness and participation motivation scales at early, mid, and late season. In contrast to previous findings, the cross-lagged correlations showed that performance and cohesion were significantly related to each other with no causal predominance of one over the other. With the exception of the friendship measure, the cross-lagged correlations were no longer significant when earlier measures of the effect variable were controlled through partial correlation and path analysis techniques. In contrast to previous research, midseason cohesion, as measured by friendship, was a significant (p < .04) predictor of late season performance. The importance of interpersonal attraction in the recruitment and maintenance of intramural team members is discussed along with the necessity for determining, in future studies, the reliability of cohesiveness measures.

We investigated the classical question of why visual acuity decreases with decreasing retinal illuminance by holding retinal eccentricity fixed while illumination varied. Our results indicate that acuity is largely independent of illuminance at any given retinal location, which suggests that under classical free-viewing conditions acuity improves as illumination increases from rod threshold to rod saturation because the retinal location of the stimulus is permitted to migrate from a peripheral location of maximum sensitivity but poor acuity to the foveal location of maximum acuity but poor sensitivity. Comparison with anatomical sampling density of retinal neurons suggests that mesopic acuity at all eccentricities and scotopic acuity for eccentricities beyond about 20°is limited by the spacing of midget ganglion cells. In central retina, however, scotopic acuity is further limited by spatial filtering due to spatial summation within the large, overlapping receptive fields of the A-II class of amacrine cells interposed in the rod pathway between rod bipolars and midget ganglion cells. Our results offer a mechanistic interpretation of the clinical metrics for low-luminance visual dysfunction used to monitor progression of retinal disease.

No abstract