ABSTRACT. The optic nerve fiber layer (NFL) of the chicken retina was studied quantitatively and morphologically at 17 positions along seven radially arranged bands from the dorsal tip of the pecten oculi using electron microscopy. The number of nerve fibers was counted in areas 6 µm in width × the full thickness of the NFL. Myelinated nerve fibers in the NFL were also identified immunohistochemically using anti-myelin basic protein serum. The dorsal area (dorsal, dorso-temporal and dorso-nasal bands) in the retina had thin NFL and contained the largest number of nerve fibers, which were mainly thin and unmyelinated. The ventral area (ventral and ventro-temporal bands) had a thick NFL and contained a relatively small number of nerve fibers, many of which were myelinated. The nasal band had the thickest NFL and contained as many nerve fibers as the dorsal area, with the temporal band showing a high ratio of myelinated fibers. The band had a thick NFL and contained many nerve fibers with a relatively low ratio of myelinated fibers. The relationship between the number and composition of nerve fibers in the NFL to the chicken visual characteristics was discussed. Although the myelin in the chicken retina was loose type, the myelin-forming cells were similar in appearance to dense oligodendrocytes. -KEY WORDS: chicken retina, morphometry, myelinated fiber, nerve fiber layer.J. Vet. Med. Sci. 61(8): 883-889, 1999 MATERIALS AND METHODS Five White Leghorn chickens, 7 to 14 months old, were used for quantitative analysis. Two chickens were anesthetized with diethyl ether and they were perfused with 1.5% glutaraldehyde in 0.1 M phosphate buffer (PB) at pH 7.4 or 3% glutaraldehyde in PB containing 1.5 mM CaCl 2 . The eyes were enucleated and opened by an encircling cut at the ora serrata, and the posterior parts were immersed in the same fixatives for another 2 hr. Three chickens were killed by cervical exsanguination under diethyl ether anesthesia, the eyes were removed as soon as possible, and the posterior half of the eye was immersed in the fixative mentioned above. The posterior half of the eye in all chickens was postfixed in 1% OsO 4 in the same buffer for 1.5 hr at 4°C. The tissues were dehydrated in ethanol. During the dehydration, seven retinal bands, radially arranged from the dorsal tip of the pecten oculi, were dissected out. These were the nasal (N), dorso-nasal (DN), dorsal (D), dorso-temporal (DT), temporal (T), ventrotemporal (VT), and ventral (V) bands. A naso-ventral band could not be obtained, because the pecten oculi occupies this place. Electron microscopic observations and measurements were carried out at 1 mm (position I) and 4 mm (position II) from the margin of the pecten oculi for all bands, and at 8 mm (position III) for N, DN and D bands (Fig. 1). Thus, morphological observations and measurements were obtained at 17 locations for each eye. The tissues were stained with lead citrate and uranyl acetate, and embedded in Epok-812. Thin sections were cut vertical to the plane of the retina. Micro...