Melanin, or products directly associated with it, regulates the matura
tion of the neural retina because in hypopigmented mammals the central
retina fails to develop fully. To determine whether this deficit is r
eflected in the distribution of photoreceptors, their topography has b
een studied in the retinae of normally reared pigmented and albino fer
rets and animals reared under reduced light conditions. In both strain
s, the general distribution of rods and cones was similar to that in t
he cat, cone density peaking in the central retina and rod density pea
king in an annulus around the area centralis. The cone population was
organized in the form of an orderly mosaic whose regularity was measur
ed at a wide range of retinal eccentricities. No differences were foun
d in cone numbers or their mosaic distribution between pigmented and a
lbino strains, either at the area centralis or at more peripheral regi
ons. In both cases order within the cone mosaic was independent of cel
l density or retinal eccentricity. In the albinos there was a signific
ant deficit in the number of rods at all retinal locations when compar
ed with rod numbers in the pigmented animals. There were no difference
s between normally reared and dark-reared animals in this respect eith
er within or between the strains. Therefore, the albino gene must have
a selective and specific effect on the development of this cell type
in the outer retina. Ganglion cells and rods are both affected by the
albino gene, while cones are not. Because cones and ganglion cells are
generated during the same period and rods are generated later, the al
bino gene cannot be acting during a particular developmental time wind
ow. Because the cone mosaic was normal in the albinos, in spite of a l
arge rod deficit, the factors that regulate the spacing of cones canno
t depend in any significant manner upon the later generation and subse
quent addition of rods to the outer retina.