The inner molecular layer (fig. 2, 4) is formed by the interlacement of the dendrites of the last layer with those of the cells of the inner nuclear layer which comes next.

The inner nuclear layer (fig. 2, 5) contains three different kinds of cells, but the most important and numerous are large bipolar cells, which send one process into the inner molecular layer, as has just been mentioned, and the other into the outer molecular layer, where they arborize with the ends of the rod and cone fibres.

The outer molecular layer (fig. 2, 6) is very narrow and is formed by the arborizations just described. The outer nuclear layer (fig. 2, 7), like the inner, consists of oval cells, which are of two kinds. The rod granules are transversely striped, and are connected externally with the rods, while internally processes pass into the outer molecular layer to end in a knob around which the arborizations of the inner nuclear cells lie. The cone granules are situated more externally, and are in close contact with the cones; internally their processes form a foot-plate in the outer molecular layer from which arborizations extend.

The layer of rods and cones (fig. 2, 9) contains these structures, the rods being more numerous than the cones. The rods are spindle-shaped bodies, of which the inner segment is thicker than the outer. The cones are thicker and shorter than the rods, and resemble Indian clubs, the handles of which are directed outward and are transversely striped. In the outer part of the rods the visual purple or rhodopsin is found.

The pigmented layer consists of a single layer of hexagonal cells containing pigment, which is capable of moving towards the rods and cones when the eye is exposed to light and away from them in the dark.

Fig. 2.—Diagrammatic section through the retina to show the several layers, which are numbered as in the text. Ct, The radial fibres of the supporting connective tissue.

Supporting the delicate nervous structures of the retina are a series of connective tissue rods known as the fibres of Müller (fig. 2, Ct); these run through the thickness of the retina at right angles to its surface, and are joined together on the inner side of the layer of nerve fibres to form the inner limiting membrane. More externally, at the bases of the rods and cones, they unite again to form the outer limiting membrane.

When the retina is looked at with the naked eye from in front two small marks are seen on it. One of these is an oval depression about 3 mm. across, which, owing to the presence of pigment, is of a yellow colour and is known as the yellow spot (macula lutea); it is situated directly in the antero-posterior axis of the eyeball, and at its margin the nerve fibre layer is thinned and the ganglionic layer thickened. At its centre, however, both these layers are wanting, and in the layer of rods and cones only the cones are present. This central part is called the fovea centralis and is the point of acutest vision. The second mark is situated a little below and to the inner side of the yellow spot; it is a circular disk with raised margins and a depressed centre and is called the optic disk; in structure it is a complete contrast to the yellow spot, for all the layers except that of the nerve fibres are wanting, and consequently, as light cannot be appreciated here, it is known as the “blind spot.” It marks the point of entry of the optic nerve, and at its centre the retinal artery appears and divides into branches. An appreciation of the condition of the optic disk is one of the chief objects of the ophthalmoscope.

The crystalline lens (fig. 1, L) with its ligament separates the aqueous from the vitreous chamber of the eye; it is a biconvex lens the posterior surface of which is more curved than the anterior. Radiating from the anterior and posterior poles are three faint lines forming a Y, the posterior Y being erect and the anterior inverted. Running from these figures are a series of lamellae, like the layers of an onion, each of which is made up of a number of fibrils called the lens fibres. On the anterior surface of the lens is a layer of epithelial cells, which, towards the margin or equator, gradually elongate into lens fibres. The whole lens is enclosed in an elastic structureless membrane, and, like the cornea, its transparency is due to the fact that all its constituents have the same refractive index.

The ligament of the lens is the thickened anterior part of the hyaloid membrane which surrounds the vitreous body; it is closely connected to the iris at the ora serrata, and then splits into two layers, of which the anterior is the thicker and blends with the anterior part of the elastic capsule of the lens, so that, when its attachment to the ora serrata is drawn forward by the ciliary muscle, the lens, by its own elasticity, increases its convexity. Between the anterior and posterior splitting of the hyaloid membrane is a circular lymph space surrounding the margin of the lens known as the canal of Petit (fig. 1, p).