We have made a fine structural investigation of the synaptic patterns made by axon terminals of retinal ganglion cells in the dorsal lateral geniculate nucleus of the cat. We compared the retinal input to dendritic processes that bear clusters of large appendages with the retinal input to relatively smooth dendritic segments that have only a few isolated spines. The study was restricted to the portion of laminae A and A1 that receive central visual field input. We were able to completely reconstruct 33 individual terminal boutons from long series of consecutive thin sections. Retinal terminals that were presynaptic to dendritic appendages tended to occupy the central position in the complex synaptic zones of geniculate fine structure called glomeruli. These terminals were surrounded by significantly more profiles than retinal terminals that were presynaptic to dendritic stems and averaged twice as many synaptic contacts per terminal bouton. The retinal input to dentritic appendages was heavily involved in a specific synaptic pattern called the triadic arrangement while retinal input to dendritic stems was only lightly involved in triads. Dendritic appendages in triads received greater synaptic input from profiles with flattened vesicles than did the dendritic stems that were found in triads.

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On the basis of an electron microscopic examination of the optic nerve of the North American opossum it was estimated that the nerve has approximately 100,000 axons, of which 98% are myelinated. The myelinated axons ranged from 0.3 to 6.7 micrometers in diamter (mean 1.6 micrometers), while unmyelinated axons were 0.2 to 1.6 micrometers in diameter (mean 0.6 micrometers). Axoplasm and axon (axoplasm plus myelin) diameter spectrums were unimodal and positively skewed. The mean of the ratio of axoplasm to axon diameter was 0.69. However, this ratio varied widely across axons and was nonlinearly distributed, decreasing with axon diameter. An inverse relationship between axon density and a high proportion of large-caliber axons was located dorsally in a cross section obtained near the eye. However, in sections obtained near the optic chiasm, regions having the highest proportion of large-diameter axons were in the ventral periphery of the nerve. It is suggested that within the 40-mm length of the nerve, there may be a change from a retinotopic organization of axons according to their diameter and central targets.

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The responses of rabbit dorsal lateral geniculate neurons to light or optic nerve shock were tested for 415 units in 43 rabbit pups 2--20 days of age. Units were driven by optic nerve shock at the youngest ages tested, but could not be driven by light until postnatal day six. Examples of each of the three prominent categories of receptive fields found in the adult were first observed at 8 days of age. Cells with receptive field properties not characteristic of the dorsal lateral geniculate nucleus of the adult were encountered until 17 days of age. The percentage of neurons with uniform and motion sensitive receptive fields approached adult levels soon after eye opening (11--12 days) but the percentage of cells with concentric receptive fields showed a steady increase throughout the neonatal period studied. The relevance of our data to the development of the visual response in the dorsal lateral geniculate nucleus and striate cortex is discussed.