This appears to me exactly what the developmental process does show according to Götte's investigations. He asserts that the retina arises from an optic plate, being the optical portion of his 'Sinnes-platte.' At an early stage this is separated by a furrow (Furche) from the general mass of epidermal cells which ultimately form the brain. This separation then vanishes, and the retina and brain-mass {102}become inextricably united into a mass of cells, which are still situated at the surface. By the closure of the cephalic plate and the withdrawal of the brain away from the surface, a retinal mass of cells is left at the surface connected with the tubular central nervous system by the hollow optic diverticulum or primary optic vesicle. If we regard only the retinal and nervous elements, and for the moment pay no attention to the existence of the tube, Götte's observation that the true retina has been formed from the optic plate (Sinnes-platte) to which the retinal portion of the brain (retinal ganglion) has become firmly fixed, and that then the optic nerve has been formed by the withdrawal of the rest of the brain (optic lobes), is word for word applicable to the description of the development of the compound retina of the arthropod eye, as has been already stated. THE SIGNIFICANCE OF THE OPTIC DIVERTICULA. The origin of the retina from an optic epidermal plate in vertebrates, as in all other animals, brings the cephalic eyes of all animals into the same category, and leaves the vertebrate eye no longer in an isolated and unnatural position. In one point the retina of the vertebrate eye differs from that of a compound retina of an invertebrate; in the former, a striking supporting tissue exists, known as Müller's fibres, which is absent in the latter. This difference of structure is closely associated with another of the same character as in the central nervous system, viz. the apparent development of the nervous part from a tube. We see, in fact, that the retinal and nervous arrangements of the vertebrate eye are comparable with those of the arthropod eye, in precisely the same way and to the same extent as the nervous matter of the brain of the vertebrate is comparable with the brain of the arthropod. In both cases the nervous matter is, in structure, position, and function, absolutely homologous; in both cases there is found in the vertebrate something extra which is not found in the invertebrate--viz. a hollow tube, the walls of which, in the case of the brain, are utilized as supporting tissues for the nerve structures. The explanation of this difference in the case of the brain is the fundamental idea of my whole theory, namely, that the hollow tube is in reality the cephalic stomach of the invertebrate, around which the nervous brain-matter was originally grouped in precisely the same manner as in the invertebrate. What, then, are the optic diverticula?