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Rod and cone visual pigments of 11 marine carnivores were evaluated. Rod, middle/long-wavelength sensitive (M/L) cone, and short-wavelength sensitive (S) cone opsin (if present) sequences were obtained from retinal mRNA. Spectral sensitivity was inferred through evaluation of known spectral tuning residues. The rod pigments of all but one of the pinnipeds were similar to those of the sea otter, polar bear, and most other terrestrial carnivores with spectral peak sensitivities (k max ) of 499 or 501 nm. Similarly, the M/L cone pigments of the pinnipeds, polar bear, and otter had inferred k max of 545 to 560 nm. Only the rod opsin sequence of the elephant seal had sensitivity characteristic of adaptation for vision in the marine environment, with an inferred k max of 487 nm. No evidence of S cones was found for any of the pinnipeds. The polar bear and otter had S cones with inferred k max of $440 nm. Flickerphotometric ERG was additionally used to examine the in situ sensitivities of three species of pinniped. Despite the use of conditions previously shown to evoke cone responses in other mammals, no cone responses could be elicited from any of these pinnipeds. Rod photoreceptor responses for all three species were as predicted by the genetic data.

It has been argued that the development and aging of the different achromatic and chromatic visual pathways may proceed independently. We review here the evidence for such independent changes with particular emphasis on electrophysiological results. Changes in chromatic and achromatic visual processing throughout the life span were studied using visual evoked potentials (VEPs). VEPs were recorded in response to the presentation of patterns designed to preferentially stimulate achromatic and S-(L+M) and (L-M) chromatic mechanisms. Recordings were made in subjects aged 1 week to 90+ years. Longitudinal measurements were obtained from several infants and cross-sectional measurements were obtained from infants and older subjects. Responses to achromatic reversing patterns at low spatial frequencies appeared early and changed rapidly. Latencies of the achromatic reversal response decreased to mature values within the first 12-15 weeks of life. Responses to chromatic pattern onsets, however, appeared later (L-M: 4 weeks; S: 6-8 weeks) and changed continuously throughout the first year of life. Chromatic waveforms from 1 year to puberty appeared inverted relative to the adult waveform. The waveforms did not appear adultlike until about 12-14 years of age. The latencies of the major negative component of the adult response reached a minimum around 17-18 years of age. Throughout the remainder of the life span, VEP latencies steadily increased and amplitudes slightly decreased. Latencies of responses to chromatic pattern onsets increased more rapidly than latencies to moderate contrast achromatic pattern reversals.