Visual Streak Research Articles

On the distribution of gamma cells in the cat retina.

Ganglion cells of the cat retina that are neither alpha nor beta cells are often lumped for convenience into a single anatomical group--the gamma cells (Boycott & Wässle, 1974; Stone, 1983; Wässle & Boycott, 1991). Defined in this way, gamma cells are the morphological counterpart to the physiological W-cell class, which includes all ganglion cells that are neither Y (alpha) nor X (beta) cells. We have estimated the retinal distribution of gamma cells by using retrograde transport to label ganglion cells innervating the superior colliculus and by assuming that these included virtually all gamma cells and no beta cells. We excluded labeled alpha cells on the basis of soma size. Our data suggest that gamma cells represent just under half of the ganglion cells in most of the nasal retina, but only about a third of those in the area centralis and temporal retina. Gamma cells do not appear to be more highly concentrated in the nasal visual streak than are other ganglion cells. In the temporal retina, gamma cells with crossed projections to the brain are apparently at least twice as common as those with uncrossed projections.

AII amacrine cell population in the rabbit retina: Identification by parvalbumin immunoreactivity

Parvalbumin (PV) is a calcium-binding protein localized to selected neurons in the nervous system, including the retina. This investigation evaluated the distribution of PV immunoreactivity in the rabbit retina using immunohistochemistry with a monoclonal antibody directed to carp PV. In the inner nuclear layer (INL), PV immunoreactivity was present in horizontal and amacrine cells. In the ganglion cell layer, PV immunostaining was confined to somata that are likely to be both displaced amacrine cells and ganglion cells. PV-immunoreactive (IR) amacrine cells were positioned in the proximal INL adjacent to the inner plexiform layer (IPL). These cells usually gave rise to a single primary process, which arborized into two distinct bands in the IPL. In sublamina a, the processes were thin and had large, irregular endings. In sublamina b, multiple processes branched from the primary process and were characterized by varicosities and spines. PV-IR amacrine cell bodies measured from 8 to 10 microns in diameter. Their density was highest in the visual streak and lowest in the periphery of the superior retina. The average number of PV-IR amacrine cells was 464,045 cells per retina (N = 3), and the average regularity index of the PV-IR cell mosaic was 3.23. PV-IR amacrine cells were further characterized by double-label immunofluorescence experiments using antibodies to PV and tyrosine hydroxylase (TH). Varicose TH-IR processes were in close apposition to many PV-IR amacrine cells and often formed "ring structures" around them. Together, these morphological, quantitative, and histochemical observations indicate that PV immunoreactivity in the INL is localized predominantly to AII amacrine cells, and therefore it is a valuable marker for the identification of this cell type.

Substance P, bombesin, and leucine-enkephalin immunoreactivities are restored in the frog tectum after optic nerve regeneration.

Extensive regeneration of the optic nerve takes place in adult Amphibia. In this study, we have determined whether one aspect of retinotectal organisation, namely immunoreactive laminae in the retinorecipient layers of the optic tectum, is restored after optic nerve regeneration. To do so, the distributions of substance-P, bombesin, and leucine-enkephalin immunoreactivities were examined in the optic tectum of the frog Litoria (Hyla) moorei. Results of a normal series were compared with those at intervals up to 84 days and at 196 days after either unilateral deafferentation or optic nerve crush. In the normal series, distinct neuropeptide immunoreactive laminae were located within the retinorecipient tectal layers. There were two major laminae with substance-P, two with bombesin, and one with leucine-enkephalin immunoreactivities. Additional faint laminae of both substance-P and bombesin immunoreactivity were present in the tectal region that receives input from the visual streak. In addition, labelling of cell bodies and dendrites was seen elsewhere in the tectum. All except one immunoreactive lamina changed after deafferentation. The deeper of those with substance-P immunoreactivity, along with both bombesin laminae, were eventually lost; the lamina with leucine-enkephalin immunoreactivity was halved in intensity. We assume that these laminae are wholely or, in the case of the leucine-enkephalin lamina, partially associated with primary optic input. By contrast, the more superficial lamina with substance-P immunoreactivity remained unchanged and is presumably not directly related to visual input. During nerve regeneration, the intensity of all laminae associated with optic input initially fell as in the deafferentation series but, in the long term, recovered to approximately 80% of normal intensities. We conclude that ganglion cells associated with each of the immunoreactivities tested had successfully regenerated. The reduced intensity of immunoreactivities after regeneration is due presumably in part to the cell loss from the ganglion cell population. Furthermore, we discuss the findings of similar studies for Rana pipiens (Kuljis and Karten [1983] J. Comp. Neurol. 217:239-251 and [1985] 240:1-15) in light of the present findings. We argue that some of the previous observations can be reinterpreted to indicate that regeneration was not limited to ganglion cells associated with substance-P immunoreactivity as first thought.

A Quantitative Study of Ganglion Cells in the German Shepherd Dog Retina

As in the number of mammals, the most prominent feature of the ganglion-cell layer in the retina of the German shepherd dog is the sharp increase in the density of ganglion cells in the central area. There is an area of maximum density and also a 'cat-like' visual streak, located dorsal to the optic disc. The isodensity lines of ganglion-cell distribution is roughly concentric. Their values vary from 5300-13,000 cells/mm2 in the central area, with the cells densely packed, to 1000 cells/mm2 or less in the periphery, where the cells are sparsely distributed. There were some individual differences amongst the animals studied, although all of them were pure-bred dogs. This suggests that the configuration of the retina in the canine species is not only dependent on the breed itself but also on some other parameters such as phylogenetic heritage, environment, aptitude, lifestyle, or even training.

Neural and behavioral effects of early eye rotation on the optokinetic system in the wallaby, Macropus eugenii

1. Total optokinetic responses measured by electro-oculography and single unit recordings from the nucleus of the optic tract and dorsal terminal nucleus (NOT-DTN) of the accessory optic system were taken from young adult wallabies, whose one eye had been rotated about the optic axis at birth, and were compared with those from normal controls. 2. The velocities of the horizontal component of the slow phases of optokinetic nystagmus were measured in the horizontal plane as a function of the direction of stimulus motion. In normal animals the overall gain during monocular stimulation was greatest for horizontal temporonasal movement, with a lesser response to movement in the opposite, nasotemporal, direction. Upward or downward vertical stimulus motion did not elicit horizontal responses. In animals where one eye was removed at birth and the other eye was normal, the characteristic bidirectional response was retained; the response was identical with that elicited from one eye of a normal animal. 3. After surgical rotation (extorsion) of the left eye by approximately 90 degrees on or within a few days of birth, the animals were grown to adulthood. The visual streak of the retina of the operated eye was then found, in individual cases, to be between 30-100 degrees from horizontal with the head held in the standard resting position. This angle was taken as the definitive degree of cyclotorsion resulting from the operation in each animal. The extraocular muscles connected with regions of the eye adjacent to the location of their outgrowth in the orbit and not with the normal point of attachment on the globe.(ABSTRACT TRUNCATED AT 250 WORDS)

Distribution of Purkinje cell-specific Zebrin-II/aldolase C immunoreactivity in the mouse, rat, rabbit, and human retina.

The developmental, genetic, and biochemical similarities that have been observed between the cerebellum and retina form the basis for ongoing investigations into retinal expression of cerebellar-specific proteins. We have examined the mouse, rat, rabbit, and human retina for expression of a protein that is present in parasagittal Purkinje cell strips and that is recognized by the antibody Zebrin-II. This protein has recently been identified as a member of the aldolase C isoenzymes. Western blotting and immunocytochemistry have been used. The monoclonal antibody Zebrin-II recognized a prominent 36 kDa protein band on immunoblots of both the cerebellum and the retina of the examined species. Immunocytochemistry showed that, in the three nonhuman species, cells were stained in the ganglion cell layer (GCL). In addition, in the mouse and rabbit, cells in the inner nuclear layer (INL) were also labeled. Except for the visual streak, there were more immunopositive cells in the rabbit GCL and INL than in corresponding areas of the mouse retina. In the human, in contrast to the other species, the photoreceptor cell layer was strongly aldolase C immunoreactive. In all species except for the rat, the photoreceptor inner segments also displayed a weak labeling. The results show that this aldolase C isoenzyme is another protein that is selectively expressed by the cerebellum and retina. Furthermore, the retinal expression is species specific, and this pattern seems to show a good correlation with the oxygenation level of the individual compartments. The indication that this aldolase C isoenzyme has specific developmental functions in the retina provides additional clues for our understanding of cerebellar organization.

Morphology and density distribution of cone photoreceptor in the retina of the atlantic stingray, Dasyatis sabina.

Light miscroscopy of the retina in the Atlantic stingray, Dasyatis sabina, reveal two distinct photoreceptor types. Histological criteria establish the two cell types as morphological rods and cones. The retina was studied through a sequential series of vertical sections in a protocol designed to evaluate the entire retina. By performing differential counts in multiple regions and expressing cones as a percent of the total photoreceptors in a domain, it was possible to determine relative cone density and distribution. Cone distribution varies throughout the retina in two patterns. First, relative cone density gradually decreases peripherally. Second, a cone-rich band occurs along the horizontal axis of the eye, extending from ora serrata to ora serrata. This structure appears to be a visual streak. Both distribution patterns are statistically significant and are consistent among animals regardless of age. © 1994 Wiley-Liss, Inc.

Anatomical characterization of retinal ganglion cells that project to the nucleus of the basal optic root in the turtle ( Pseudemys scripta elegans)

There is little detailed information about retinal ganglion cells which project to specific central targets in the brain. The present study examined retinal ganglion cells projecting to the nucleus of the basal optic root, a major accessory retinal target in the turtle. These ganglion cells were first selectively labeled using retrograde transport of rhodamine injected stereotaxically into the nucleus of the basal optic root. The number and distribution of the retrogradely labeled cells in the retina was then determined. Some of these retrogradely labeled cells were then injected intracellularly with Lucifer Yellow, photoconverted using diaminobenzidine, and drawn in detail using a camera lucida attachment. There were approximately 1500 ganglion cells in each retina which projected to the nucleus of the basal optic root, of which 20% had cell bodies displaced to the inner nuclear layer. More than 50% of the total population was concentrated in the visual streak region. All ganglion cells projecting to the nucleus of the basal optic root, both normal and displaced, had monostratified dendritic arborizations in stratum 1 of the inner plexiform layer. About 41% of these ganglion cells had elongated dendritic arborizations with distinct orientations, which may suggest a correlation of morphology and function. There were similarities in the overall appearance, and in the type and stratification of the dendritic arborizations of all ganglion cells projecting to the nucleus of the basal optic root. These anatomical similarities are consistent with the previously demonstrated similarities in physiology and may reflect a common role for these ganglion cells in visual processing.

Distribution and coverage of A- and B-type horizontal cells stained with Neurobiotin in the rabbit retina.

Both A- and B-type horizontal cells in the rabbit retina were labeled by brief in vitro incubations of the isolated retina in the blue fluorescent dye 4,6-diamino-2-phenylindole. Intracellular injection of Lucifer Yellow into the somata revealed the morphology of the individual cells. Dye-coupling with Lucifer Yellow was seen only between A-type horizontal cells. By contrast, injection of the tracer Neurobiotin showed dye-coupling between both A- and B-type horizontal cells. There also appeared to be coupling between the axon terminals of B-type horizontal cells. The extensive dye-coupling seen following injection of Neurobiotin into a single horizontal cell soma can be used to obtain population counts of each cell type. Staining of large numbers of each cell type across the retina showed that each type increased in number and declined in dendritic diameter as the visual streak was approached, such that relatively constant coverage across the retina was maintained. In the visual streak, A-type horizontal cells numbered 555 cells/mm2 and averaged 120 microns in diameter, compared to 1375 cells/mm2 and 100 microns for B-type horizontal cells. In the periphery, the A- and B-types numbered 250 cells/mm2 and 400 cells/mm2, respectively. The average diameters of the dendritic trees at these locations were 225 microns for the A-type and 175 microns for the B-type. Coverage across the retina averaged almost six for A-type horizontal cells and 8-10 for the B-type. A-type horizontal cells in the visual streak whose elliptical dendritic fields were shown by Bloomfield (1992) to correlate physiologically with orientation bias were shown to be dye-coupled to cells with symmetrical dendritic fields.

Retinal ganglion cell axon diameter spectrum of the cat: mean axon diameter varies according to retinal position.

Axon diameters of retinal ganglion cells were measured from electron micrographs of the nerve fiber layer of the cat. Three adult retinae were examined which had mean axonal diameters of 1.18 +/- 0.86 (n = 5553), 1.12 +/- 0.79 (n = 7265), and 1.47 +/- 1.11 microns (n = 10,867). Cumulative histograms from several locations adjacent to the optic disc were unimodal (modal peaks: 0.6-0.8 microns). This unimodal distribution, however, did not reflect the regional differences in axonal diameters found throughout the retina. In many locations, especially those related to axons of the temporal retina, axon diameter distributions were clearly bimodal or even trimodal (modal peaks: 0.6-0.8, 1.4-2.1, and 3.3 microns). Measurements from one retina indicated that the mean diameters of axons arising from the area centralis and visual streak (0.94 +/- 0.63 and 0.98 +/- 0.68, respectively) were not significantly different from each other; however, when compared to other areas around the optic disc, the percentage of fibers with diameters between 1.5-2.0 microns was highest in the sample adjacent to the area centralis. Axons temporal to the optic disc were found to be on average larger than those nasal to the optic disc; similarly superior axons were larger than inferior axons. Axonal distributions at the retinal periphery were found to be significantly different from those at the optic disc (P < or = 0.05) and contained a higher percentage of medium-sized axons and fewer small axons. In each of the three retinae the proportions small, medium, and large axons were respectively gamma: 46; 47; 48, beta: 50; 49; 48, and alpha: 4; 4; 4; regional differences in the proportions of each axonal class are compared to previously published ganglion cell density maps. Differences between axonal bundles within each sample location were not significantly different; however, in one retina axons in the scleral half of the fiber layer were significantly larger (P < or = 0.01) than axons in the vitreal half of the nerve fiber layer adjacent to the optic disc. When compared to the axonal diameter distributions found within the optic nerve (Cottee et al., 1991) and optic tract (Reese et al., 1991), our data indicates that the diameter of retinal axons may increase by up to 30% along the length of the visual pathway.

Orientation-sensitive amacrine and ganglion cells in the rabbit retina

1. Intracellular recordings were obtained from amacrine and ganglion cells in the isolated, superfused retina-eyecup preparation of the rabbit to test the orientation sensitivity of their responses. Cell identification was based on morphological criteria following injection of horseradish peroxidase (HRP) or N-(2-aminoethyl)-biotinamide hydrochloride (Neurobiotin) to visualize soma-dendritic architectures. 2. In terms of the physiological mechanisms generating their sensitivity, two types of orientation-sensitive amacrine cell and a single type of orientation-sensitive ganglion cell were found. These cell types were termed orientation selective and orientation biased. Cells were subtypes further into on- or off-center receptive-field categories. 3. The receptive fields of orientation-selective amacrine and ganglion cells were composed of two inhibitory fields that flanked the excitatory center receptive field along the preferred orientation. These inhibitory flanks produced a center receptive-field anisotropy with its major axis corresponding to the preferred orientation: either parallel or orthogonal to the visual streak. When a stimulus was oriented orthogonal to the preferred orientation (i.e., at the null orientation), the inhibitory fields were stimulated, resulting in a null inhibition that blocked the center-mediated excitation. Stimulation of these inhibitory flanks was absolutely essential to evoke the orientation selectivity of these cells. The null response reflected inhibition associated with a conductance increase and not disfacilitation. 4. Orientation-biased amacrine cells displayed a center receptive-field anisotropy with its major axis oriented either parallel or orthogonal to the visual streak. These cells preferred light stimuli oriented along the major axis of the center receptive field. However, whereas the excitatory response of these cells was reduced when a stimulus was rotated from the preferred orientation, there was no corresponding hyperpolarization. No null inhibition was detected even after modulation of the membrane potential with extrinsic current. 5. Although orientation-biased amacrine cells were morphologically heterogeneous, they all displayed dendritic arbors that were markedly elongated along an axis corresponding to their physiological preferred orientation. Thus it appears that the elongated dendritic fields of these cells may provide for the anisotropy of their center receptive fields and, in turn, their orientation sensitivity. 6. Orientation-selective amacrine cells formed a rather homogeneous morphological group of cells. These neurons displayed large, radially symmetric dendritic arbors with diameters averaging 1,100 microns. There were no asymmetries in their dendritic fields and thus no clear structural basis for their orientation selectivity. 7. In contrast, orientation-selective ganglion cells displayed diverse soma-dendritic architecture and thus could not be placed into a single morphological class.(ABSTRACT TRUNCATED AT 400 WORDS)

Radial asymmetry in the topography of retinoblastoma. Clues to the cell of origin.

Retinoblastoma is a malignancy of the human developing retina. In situ as well as in vitro studies have attributed tumoral histogenesis either to a primitive retinoblast with neuronal and glial differentiation potentials, or to a photosensory progenitor cell. Here it is shown in vivo that the retinal topography of 457 retinoblastoma and retinoma foci is radially asymmetrical. Tumor density appears to mimic the horizontal visual streak characteristic of red/green cone cell distribution. Such a non-random distribution seems to invalidate the hypothesis of a primitive multipotential neuroblast as the unique source of retinoblastoma and may support the view that retinoblastoma evolves along the cone cell lineage.

Computer Aided Near Earth Object Detection

The Spacewatch program at the University of Arizona has pioneered automatic methods of detecting Near Earth Objects. Our software presently includes three modes of object detection: automatic motion identification; automatic streak identification; and visual streak identification. For automatic motion detection at sidereal drift rates, the 4σ detection threshold is near magnitude V = 20.9 for nearly stellar asteroid images. The automatic streak detection is able to locate streaks whose peak signal is above ~4σ and whose length is longer than about 10 pixels. Some visually detected streaks have had peak signals near ~1σ.Between 1990 September 25 and 1993 June 30, 45 new Near Earth asteroids, two comets and two Centaur's have been discovered with the system. An additional six comets, five Near Earth asteroids, and one Centaur were also “re-discovered”. The system has directly detected for the first time Near Earth Objects in the complete size range from about 5 kilometers to about 5 meters. Each month ~2,000 main belt asteroids are also detected.Future upgrades in both hardware, software, and telescope aperture may allow an order of magnitude increase in the rate of discovery of Near Earth Objects in the next several years. Several of the techniques proposed for the Spaceguard Survey have already been tested by Spacewatch, and others will need to be tested in the near future before such a survey can be implemented.

Some optical features of the eyes of stomatopods

The optics of a variety of stomatopod eyes has been investigated using goniometric eye-mapping techniques and anatomical measurements. The species examined come from 3 of the 4 existing superfamilies: the Gonodactyloidea, Lysiosquilloidea and Squilloidea. This paper examines acuity, optical axes and general features of eye shape. Stomatopod eyes are divided into 3 clearly distinct zones; the mid-band and two hemispheres. Each hemisphere consists of an edge region, a "visual streak" and a near mid-band region. The optical axes of many ommatidia from both hemispheres are skewed inwards towards the centrally placed mid-band and are rarely normal to the corneal surface. The large skew angle enables each hemisphere to examine an area which extensively overlaps that of the other hemisphere. As a result monocular distance judgement is possible. Most of the ommatidia in each hemisphere are part of a horizontally aligned but vertically acute "visual streak" area. There is one "visual streak" per hemisphere and both look into the same 5-10° strip. This narrow strip is also the area in space the mid-band ommatidia examine. An acute zone is present in the eyes of lysiosquilloid and gonodactyloid stomatopods and includes ommatidia, from both the hemispheres and the mid-band. Here inter-ommatidial angles, especially those in the horizontal direction, are reduced. Acute zone facets are enlarged to increase sensitivity rather than aid spatial resolution.

Some optical features of the eyes of stomatopods

The optics of a variety of stomatopod eyes has been investigated using goniometric eye-mapping techniques and anatomical measurements. The species examined come from 3 of the 4 existing superfamilies: the Gonodactyloidea, Lysiosquilloidea and Squilloidea. This paper examines acuity, optical axes and general features of eye shape. Stomatopod eyes are divided into 3 clearly distinct zones; the mid-band and two hemispheres. Each hemisphere consists of an edge region, a “visual streak” and a near mid-band region. The optical axes of many ommatidia from both hemispheres are skewed inwards towards the centrally placed mid-band and are rarely normal to the corneal surface. The large skew angle enables each hemisphere to examine an area which extensively overlaps that of the other hemisphere. As a result monocular distance judgement is possible. Most of the ommatidia in each hemisphere are part of a horizontally aligned but vertically acute “visual streak” area. There is one “visual streak” per hemisphere and both look into the same 5–10° strip. This narrow strip is also the area in space the mid-band ommatidia examine. An acute zone is present in the eyes of lysiosquilloid and gonodactyloid stomatopods and includes ommatidia, from both the hemispheres and the mid-band. Here inter-ommatidial angles, especially those in the horizontal direction, are reduced. Acute zone facets are enlarged to increase sensitivity rather than aid spatial resolution.

Transient neovascularisation of the frog retina during optic nerve regeneration.

In conditions such as diabetic retinopathy, degenerative events in the retina are associated with neovascularisation. It is well established that a proportion of retinal ganglion cells die during optic nerve regeneration in the frog. The present study has determined whether neovascularisation takes place during this regenerative process. To do so, the pattern of blood vessels overlying the retinal ganglion cell layer was analysed in the frog Litoria (Hyla) moorei. We examined normal animals and those undergoing optic nerve regeneration following nerve crush. Blood vessels were visualised by perfusion with Indian ink and retinae were prepared as wholeamounts. In normal animals, the vascular tree was found to lie superficial to the nerve fibre layer and was more complex in regions overlying the area centralis and visual streak. After nerve crush, abnormal blood vessels transiently formed between the existing branches of the vascular tree. The new vessels were concentrated as an annulus centred on the optic nerve head and over the area centralis in midtemporal retina. The neovascularisation became most extensive between 6 and 10 weeks postcrush and disappeared by 12 weeks. The spatiotemporal sequence of neovascularisation suggests that it is triggered by accumulations of degenerating material formed as a proportion of the ganglion cells die during optic nerve regeneration.

A quantitative study of the lateral spread of Müller cell responses to retinal lesions in the rabbit.

A wide variety of retinal pathology is associated with an increase in Müller glial cell expression of glial fibrillary acidic protein (GFAP). In this study the time course and spatial spread of the Müller cell GFAP response following argon laser photocoagulation lesions was examined in wholemounted rabbit retina. At 24 hours single focal lesions were surrounded by GFAP positive Müller cell end feet which declined in density with distance but extended as far as 2-3 mm from the lesion. The Müller cell reaction reached a maximal spread of 4-5 mm at 14 to 21 days and had started to contract by 30 days, leaving a core of GFAP positive processes immediately around the lesion site at 60 days. This zone of spread was much larger than the area of disrupted pigment epithelium. Isodensity plots did not reveal any correlation with the trajectory of retinal ganglion cell axons. The spread of reaction was more confined for lesions within the visual streak than in the dorsal or ventral retinal periphery. Multiple lesions within a focal region of retina resulted in a greater density of GFAP reactive end feet with a corresponding greater spread. However, when five to ten lesions were made in a horizontal row, the Müller cells over the entire retina became GFAP immunoreactive. This pan-retinal reaction took several days to spread, peaked at 7-14 days, and contracted back to the primary lesion sites by 2 months. This spread of Müller cell reactivity may be triggered by the diffusion of substances released by injury or it may be due to direct cellular communication. The extensive indirect effect on Müller cells of laser irradiation might be an important component of the clinical effect of laser photocoagulation and indicates a long distance communication mechanism between retinal glia which is poorly understood. This study also shows the importance of the time at which the Müller cell response is assessed.

Geometry of the representation of the visual field on the superior colliculus of the wallaby (Macropus eugenii). I. Normal projection

In 13 wallabies (Macropus eugenii, the tammar), microelectrode recordings of the activity of units in the superficial layers of the superior colliculus in response to a flashing light spot were used to make a map of the spatial location of their receptive fields. This article describes the projection of a normal eye to the contralateral colliculus. Ten of the 13 animals had one rotated eye and these projections are analysed in the accompanying paper (James et al., this issue). Units responded briskly to the stimulus at light on and off and had receptive fields about 5 degrees across. The centres of receptive fields from a regular array of recording points on the colliculus were plotted with a perimeter and fitted to a flattened representation of the colliculus according to a spline technique. The visual field of each colliculus extends from 25 degrees ipsilateral to the vertical meridian to 120 degrees temporal contralaterally. The lines of isoazimuth are regularly spaced and parallel and run mediolaterally on the colliculus. The horizon is represented by a line running rostrocaudally and the parallels are more widely spaced near the horizon and become compressed in the superior and inferior fields. The variation of areal magnification factor fits the distribution of density of retinal ganglion cells very well. Anisotropy of the projection means that the increased ganglion cell density of the retinal visual streak is entirely accommodated by magnification in the vertical direction, while the magnification of the azimuthal projection is equal over the whole field. No responses were recorded from the ipsilateral eye even though anatomically there is a direct retinal ipsilateral projection.

Heterogeneity of synaptic density in the adult pigmented rabbit's visual cortex.

In the adult pigmented rabbit, synaptic density in the lateral and medial part of the visual cortex was estimated along the projection area of the visual streak. A higher synaptic density distribution was observed in the lateral cortex (projection area of the nasal visual field) than in the medial cortex (projection area of the temporal visual field). This shows that there is a higher synaptic density in the region of the visual cortex receiving input from a retinal area with a high ganglion cell concentration than the area of the cortex receiving input from the retina with a low concentration of such cells. The regions of the visual cortex with higher and lower synaptic densities are the areas having a higher and lower magnification factor respectively.

Visual acuity in the horse

We assessed the ease with which horses could learn visual discriminations and measured their resolution acuity. We trained three horses to press their noses against one of two large wooden panels to receive a small food reward. Following training on a series of two-choice discrimination tasks, resolution acuity was measured. Although there was some variability between animals, the best acuity obtained was 23.3 c deg −1. Within the margin of error imposed by limited anatomical data, the obtained values are consistent with predictions based on retinal ganglion cell density estimates and posterior nodal distance/axial length ratios. They suggest that the resolution acuity of the horse is limited by ganglion cell density in the temporal portion of the narrow visual streak.