Influence of Binocular Visual Anomalies on Reading in First Grade School Children with High Visual Acuity.

The aim of this study was to describe the binocular visual status of first grade children with high binocular visual acuity. The results have shown that only 5.1% of children had normal binocular vision, 25.7% had only moderate and 67.9% had severe and moderate binocular anomalies. Significant differences were revealed between students with poor reading and with normal reading with respect to reduced convergence (P < 0.001), and mean scores of behavior symptom numbers, indicating the presence of binocular visual anomalies (P < 0.002).

A multivariate approach to structural heterogeneity of retinal ganglion cells.

Knowing neuronal types is essential for understanding the structural and functional organization of the nervous system. It has long been recognized that neuronal types should be discovered and not defined. This can be done using cluster analysis (CA). Despite there being many studies using CA to classify neurons, only a few of them meet its formal prerequisites. In the present study, we provide an example of using CA in combination with other multivariate techniques for examining neuronal diversity. A special emphasis is put on formal prerequisites to the data and procedure. The data under scrutiny are a sample of ganglion cells projecting to the basal optic nucleus [accessory optic system-projecting ganglion cells (AOS GCs)] in the common frog. There is physiological evidence that these cells comprise at least two functional types but their structural heterogeneity has not been addressed. Cells were labeled with horseradish peroxidase in vivo and examined in whole-mounted retinae using light microscopy. A sample of well-stained cells was obtained and used to estimate 18 structural parameters. A variety of clustering algorithms were used to classify the cells. The joint polar distribution of dendrite mass was monomodal. CA did not reveal a statistically reliable cluster structure in the sample. The clusters were not cohesive and well isolated. ANOVA-on-Ranks revealed no significant between-cluster differences. Our formal conclusion is that functionally distinct frog AOS GCs do not differ in morphology or dendritic arbor orientation. The advantages and limitations of the adopted approach are discussed.

Morphology and spatial arrangement of large retinal ganglion cells projecting to the optic tectum in the perciform fish Pholidapus dybowskii.

Using retrograde HRP labeling from the optic nerve (ON) or optic tectum (OT), we have visualized large ganglion cells (LGCs) in wholemounted retinas of the teleost Pholidapus dybowskii and studied their morphology and spatial properties. In all, three LGC types were distinguished. In a previous paper, detailed data were provided on one type, biplexiform cells [Pushchin, I. I., & Kondrashev, S. L. (2003). Biplexiform ganglion cells in the retina of the perciform fish Pholidapus dybowskii revealed by HRP labeling from the optic nerve and optic tectum. Vision Research, 43, 1117-1133]. Here, we present data on the other two confirmed types, alpha(a) and alpha(ab) cells. The types differed in the level of dendrite stratification, dendrite arborization pattern, dendritic field size, and other features, and formed in the retina significantly non-random, spatially independent mosaics. Both types were labeled from the OT, indicating their participation in OT-mediated visual reactions. The comparison of spatial properties of alpha(a) and alpha(ab) mosaics labeled from the ON and OT suggests that the OT is the major or one of the major projection areas of both types. We also describe the morphology of cells resembling alpha(c) cells of other fishes, which were only labeled from the ON. The LGC types presently revealed were similar in their morphology to LGCs found in other teleosts supporting the hypothesis of LGC homology across the teleost lineage.

Evidence for spatial regularity among retinal ganglion cells that project to the accessory optic system in a frog, a reptile, a bird, and a mammal.

The vertebrate retina contains only five major neuronal classes but these embrace a great diversity of discrete types, many of them hard to define by classical methods. Consideration of their spatial distributions (mosaics) has allowed new types, including large ganglion cells, to be resolved across a wide range of vertebrates. However, one category of large ganglion cells has seemed refractory to mosaic analysis: those that project to the accessory optic system (AOS) and serve vestibulocerebellar mechanisms of motion detection and image stabilization. Whenever AOS-projecting cells have been analyzed by nearest-neighbor methods, their distribution has appeared almost random. This is puzzling, because most aspects of visual processing require the visual scene to be sampled regularly. Here, spatial correlogram methods are applied to distributions of large ganglion cells, labeled retrogradely from the AOS in frogs, turtles, and rats, and to the AOS-projecting displaced ganglion cells of chickens. These methods reveal hidden spatial order among AOS-projecting populations, of a form that can be simulated either by superimposing a single regular mosaic on a random population or, more interestingly, by overlapping three or more regular, similar but spatially independent mosaics. The rabbit is known to have direction-selective ganglion cells (not, however, AOS projecting) that can be subdivided into functionally distinct, regular mosaics by their tracer-coupling patterns even though they are morphologically homogeneous. The present results imply that the direction-selective AOS-projecting ganglion cells of all vertebrates may, likewise, be subdivided into regular, independent mosaics.

Species-dependent variation in the dendritic stratification of apparently homologous retinal ganglion cell mosaics in two neoteleost fishes.

Large retinal ganglion cells of the marine neoteleost Bathymaster derjugini were labeled with horseradish peroxidase and studied in flatmounts. Four types formed regular, independent mosaics, of which three (biplexiform, alpha-a, alpha-c) resembled those in several other teleosts. The fourth (alpha-ab) appeared novel in one significant respect. Whereas we originally described similar cells in another neoteleost, Oreochromis spilurus, as monostratified in sublamina b of the inner plexiform layer, these were very clearly bistratified in a and b. Detailed re-analysis of our Oreochromis flatmounts showed that the difference is of one degree only: many Oreochromis cells do send fine dendrites into a. These observations strengthen the evidence that all four mosaics are homologous across a wide range of fishes, and clear away an obstacle to our earlier proposals that the alpha-a, alpha-ab and alpha-c mosaics of fishes, frogs, and perhaps other nonmammalian jawed vertebrates too, may all be homologous.

Biplexiform ganglion cells, characterized by dendrites in both outer and inner plexiform layers, are regular, mosaic-forming elements of teleost fish retinae.

Biplexiform ganglion cells were labelled by retrograde transport of HRP in five species of marine fish from the neoteleost acanthopterygian orders Perciformes and Scorpaeniformes. Their forms and spatial distributions were studied in retinal flatmounts and thick sections. Biplexiform ganglion cells possessed sparsely branched, often varicose, dendrites that ramified through the inner nuclear layer (INL) to reach the outer plexiform layer (OPL), as well as conventional arborizations in the most sclerad part of the inner plexiform layer (IPL). Their somata were of above-average size and were displaced into the vitread border of the INL. Mean soma areas ranged from 99 +/- 6 microns2 in Bathymaster derjugini (Perciformes) to 241 +/- 12 microns2 in Hexagrammos stelleri (Scorpaeniformes), but were similar in each species to those of the outer-stratified alpha-like ganglion cells, whose dendritic trees occupied the same IPL sublamina. In the best-labelled specimens, biplexiform cells formed clear mosaics with spacings and degrees of regularity much like those of other large ganglion cells, but spatially independent of them. Biplexiform mosaics were plotted in three species, and analyzed by nearest-neighbor distance and spatial correlogram methods. The exclusion radius, an estimate of minimum mosaic spacing, ranged from 113 microns in Hexagrammos stelleri, through 150 microns in Ernogrammus hexagrammus (Perciformes), to 240 microns in Myoxocephalus stelleri (Scorpaeniformes). A spatial cross-correlogram analysis of the distributions of biplexiform and outer-stratified alpha-like cells in Hexagrammos demonstrated the spatial independence of their mosaics. Similar cells were previously observed not only in the freshwater cichlid Oreochromis spilurus (Perciformes) but also in the goldfish Carassius auratus (Cypriniformes) which, being an ostariophysan teleost, is only distantly related. Thus, biplexiform ganglion cells may be regular elements of all teleost fish retinae. Their functional role remains unknown.

Morphology of bipolar cells and their participation in spatial organization of the inner plexiform layer of jack mackerel retina.

Morphology of bipolar cells in the jack mackerel retina [Trachurus mediterraneus ponticus (Aleev)] was investigated by the Golgi method. Eight types of bipolar cells are described. It is the first time that cells with an unbranched main dendrite are found in fish retina. It is shown that the inner plexiform layer of the jack mackerel retina contains regular lattices, located at 5 levels and conserted in a characteristic way with the cone mosaic. These lattices are formed by swellings of bipolar cell axons. It is shown that only bipolar cells with small dendritic aborizations (less than or equal to 14 micron dia) take part in this organization.

Inner plexiform layer of jack mackerel retina: participation of amacrine and ganglion cells in its spatial organization.

In the jack mackerel retina (Trachurus mediterraneus ponticus) the inner plexiform layer demonstrates a very high degree of differentiation and contains not less than 25 sublayers. Investigation with Golgi method revealed many varieties of neurons, which are responsible for the structural organization of the inner plexiform layer. There are 8 types of bipolar cells, 24 types of amacrine cells and 7 types of ganglion cells with layered processes. The branching levels of the processes of these neurons were determined. Several varieties of neurons are described for the first time.