Christine A. Curcio

The spatial resolution capacity of human foveal retina

An image on the retina of a human eye enters the visual system through an array of photoreceptors that sets the boundaries on the spatial detail available for neural representation. In order to investigate the extent to which the input spatial detail is preserved by the human neural system, we compare the anatomical spatial limits as determined by the Nyquist frequency, the highest spatial frequency reconstructable from the cone array, and measures of human acuity, the minimum angle resolvable. We find that the anatomical Nyquist limits determined along the temporal horizontal meridian of a well-studied human retina (Curcio, Sloan, Packer, Hendrickson & Kalina, 1987b) offer a reasonable prediction of human acuity within the retinal region extending from slightly off the exact foveal center to about 2.0 deg of retinal eccentricity. However, we find a narrow peak of anatomical resolution at the foveal center where the acuity appears to be overestimated by cone spacing.

A whole mount method for sequential analysis of photoreceptor and ganglion cell topography in a single retina

Photoreceptors (PR) in human and monkey retina are visible in whole mounts cleared with glycerol or dimethyl sulfoxide and viewed with Nomarski differential interference contrast microscopy. These preparations substantially decrease the large tissue volume changes associated with dehydration and sectioning and reveal many details of PR organization and cytology with great clarity. Tissue may be subsequently stained to reveal ganglion cells so that the topography of both cell types may be studied in the same retina.

Computer methods for sampling, reconstruction, display and analysis of retinal whole mounts

We are quantifying the distribution of photoreceptors and ganglion cells in human retina with the goal of establishing a reliable anatomical database which may be compared to information about visual function. We required a representation of retinal cell distributions which facilitated collection, analysis, and display of morphometric data from the entire retina of a large number of eyes. We report computer methods to (1) reconstruct the original retinal sphere from a three-piece whole mount preparation; (2) sample the retina in a manner which allowed description of approximately radially symmetrical cell distributions and avoided both undersampling (which produces interpolation artifacts) and oversampling (which wastes time); (3) interpolate between data points in order to produce plots of cell density along arbitrary meridians and maps of average cell density from several eyes; (4) specify locations on the retinal surface using a spherical coordinate system with its primary axis through the fovea; and (5) produce color-coded maps of cell distributions in a standard perimetric projection.

Variation in longevity of rats: Evidence for a systematic increase in lifespan over time

Male-Sprague-Dawley rats (CrL:CD(SD)BR) were maintained under barrier conditions at Charles River Breeding Laboratories (Wilmington MA) from August, 1975, to July, 1983. Animals were provided food and water ad libitum. Survival data from 8 completed cohorts of 100 animals each and one continuing cohort reveal a highly significant linear increase in median lifespan, yielding a 26% increase in this parameter for cohorts born over a period of less than six years. The biological factors responsible for this increase are not clear at present. Nevertheless, these results in outbred rats, taken in conjunction with previous observations of a trend towards increased longevity in inbred mice, indicate that the assumption of cohort equivalence underlying many cross-sectional studies of biological aging may not be valid.