Retinal projections in the freshwater butterfly fish, Pantodon buchholzi (Osteoglossoidei). II. Differential projections of the dorsal and ventral hemiretinas.

Pantodon buchholzi, the freshwater butterfly fish, is a member of the Osteoglossomorpha, the most primitive of the four major teleost radiations. The projections of fibers originating in the dorsal and ventral hemiretinas in Pantodon, as determined with autoradiography, are reported here. Fibers originating in the ventral hemiretina reach their targets through the axial, medial and dorsal optic tracts. Fibers that originate in the dorsal hemiretina reach their points of termination by way of the axial, medial and ventral optic tracts. Projections of the various tracts to preoptic, thalamic, tubercular, pretectal and tectal regions, as described in the previous study of total retinal projections, were verified. The retinal projections to the preoptic, thalamic and tubercular nuclei do not map topographically. Ventral hemiretinal fibers are mapped, however, onto the dorsal part of the nucleus pretectalis superficialis pars parvocellularis, the rostral part of the dorsal accessory optic nucleus, the entire nucleus pretectalis periventricularis pars ventralis and the dorsomedial portion of the optic tectum. Ventral hemiretinal fibers also supply most if not all the retinal innervation to the central pretectal nucleus. In contrast, dorsal hemiretinal fibers are mapped onto the ventral part of nucleus pretectalis superficialis pars parvocellularis, the entire dorsal accessory optic nucleus and the ventrolateral portion of the optic tectum. The dorsal and ventral hemiretinal projections to the tectum about at a cytoarchitectonically recognizable point, indicating that no discontinuity is present in the retinal connectivity with the tectum. The pars parvocellularis of nucleus pretectalis superficialis is a simple, unfolded, and nonlaminar structure in Pantodon. This structure contrasts markedly with the more complex, folded structure of the nucleus in the majority of other examined teleosts. The orientation of the projections from the dorsal and ventral hemiretinas onto this nucleus in Pantodon is congruent with that seen in other fishes only after a schematic unfolding of the nucleus in these fishes.     

Two visual pathways to the telencephalon in the nurse shark (Ginglymostoma cirratum). I. Retinal projections

The central projections of the retina in the nurse shark were studied by anterograde transport of horseradish peroxidase and tritiated proline. With regard to efferent retinal fibres, both techniques gave completely identical results. Projections were found to pretectal area, dorsal thalamus, basal optic nucleus, and optic tectum, all at the contralateral side. The retinal target cells in the dorsal thalamus are restricted to the ventrolateral optic nucleus and the posterior optic nucleus. No evidence was found for an earlier-reported projection to the lateral geniculate nucleus. The present findings show that the ventrolateral optic nucleus exhibits homological features of the dorsal lateral geniculate nucleus in other vertebrate groups, whereas the lateral geniculate nucleus of the nurse shark is much more comparable to the nucleus rotundus of teleosts and birds and would be more appropriately so named. The application of the HRP technique also allowed us to study afferents to the retina by retrograde transport of tracer. Retrogradely labeled cells were observed in the contralateral optic tectum and are apparently similar to those reported for teleosts and birds.     

Connections of the visual cortex in the hedgehog (Paraechinus hypomelas). I. Thalamocortical projections

Visual thalamocortical projections were studied in the Pakistani hedgehog with anterograde degeneration techniques following large aspiration lesions and discrete electrolytic lesions of visual thalamic nuclei. After 3- to 9-day survival periods, the brains were processed and stained with the Fink-Heimer technique, and examined with the light microscope. The resutls of these studies show that there are at least four separate thalamic nuclei that project to visual cortex in the hedgehog. First, the dorsal lateral geniculate nucleus projects with a topographic order to layer IV and the adjacent portion of layer III of striate cortex. Second, a thalamic transition zone, adjacent to the dorsal lateral geniculate nucleus, projects widely to layer VI throughout striate cortex and possibly to all laminae of striate cortex in the area lying just medial to the striate-parastriate border. The laminar pattern of termination of this transition zone is similar to that of the lateral posterior nucleus. Third, the lateral posterior nucleus projecs with little discernible topographic localization to layer VI of both striate and parastriate cortex, and in addition, to the remaining laminae of parastriate cortex except the outer one-half of layer I. Fourth, the anterior intralaminar region projects to the outer one-third to one-half of layer I in both striate and parastriate cortex. Evidence derived from ablations of the entire thalamus on one side suggests that there may be still another thalamic nucleus that projects to visual cortex in the hedgehog.     

The visual system of the channel catfish (Ictalurus punctatus). I. Retinal ganglion cell morphology

Horseradish peroxidase was applied to lesions in the optic nerve of catfish (Ictalurus punctatus). The retinae were processed to reveal HRP-labelled ganglion cells. The histochemical techniques employed allowed fine details of the dendritic arbor to be resolved. Flat-mounted retinae were examined and the following characteristics were noted in individual ganglion cells: Soma area, shape, and depth; number and diameter of major dendrites; shape, area, and depth(s) within the inner plexiform layer (ipl) of the dendritic arbor; origin of the axon (from the soma or a dendrite). On the basis of these characteristics, eleven classes of ganglion cells were delineated: four classes of giant cells (G1-G4) and seven classes of smaller cells (S1-S7). G1 cells had dendrites arborizing in the most distal sublamina of the ipl. G1 cells in the dorsal retina had nasotemporally elongated dendritic arbors. G2 cells had dendrites in the proximal portion of the ipl. G3 cells were almost completely confined to a band running between the nasal and temporal retinal poles, through the center of the retina. In this location, the cells had dorsoventrally elongated dendritic arbors, which were bistratified in the ipl. G4 cells were displaced into the inner nuclear layer. S1 and S4 cells had axons arising from their somata, and dendrites arborizing in the distal and the proximal ipl, respectively. S2 cells were typified by their unstratified dendritic arbors. Similarly, S3 cells were characterised by their bistratified arbors. S5 cells arborized in the most proximal ipl sublamina. S6 cells were small ganglion cells with their somata lying in the inner nuclear layer. S7 cells tended to have complex dendritic arbors, and their axons arose from dendrites.     

Auditory pathways in the budgerigar. I. Thalamo-telencephalic projections

Thalamo-telencephalic auditory pathways in the budgerigar (Melopsittacus undulatus) were studied using horseradish peroxidase (HRP) histochemistry and amino acids autoradiography. The results indicate that in this species the thalamic auditory relay nucleus, n. ovoidalis, projects upon a circumscribed region of the caudal and caudomedial neostriatum including field 'L' and immediately adjacent portions of the neostriatum intermedium, pars dorsolateralis (NIDL). This region of NIDL also receives inputs from another thalamic nucleus, n. dorsolateralis posterior (DLP). In the DLP is in receipt of tectal inputs. Projections of DLP upon NIDL were confirmed with amino acids autoradiography. The results of the HRP experiments indicate that different portions of n. ovoidalis project upon different portions of field 'L' and NIDL. Neurons in the dorsal and lateral portions of the n. ovoidalis project upon more medial portions of field 'L'. Neurons located centrally in the n. ovoidalis project upon central and lateral portions of field 'L'. Neurons in the ventromedial portion of the n. ovoidalis are labeled in all cases in which HRP is placed in either field 'L' or in the DLP projection field immediately adjacent to field 'L' proper. HRP injections placed in NIDL lateral to the projection fields of the n. ovoidalis and DLP label neurons within other diencephalic nuclei including the n. subrotundus. The caudal and intermediate levels of the neostriatum intermedium apparently serve as a complex processing area for many thalamic inputs in this species. The existence of multiple ascending thalamo-telencephalic projections from portions of the thalamus receiving inputs from both the visual (i.e., tectal) and auditory (i.e., n. mesencephalicus lateralis pars dorsalis) portions of the midbrain roof (i.e., from DLP and from n. ovoidalis) suggests the possibility that intermodal associations may take place in these telencephalic fields. Such partially converging pathways may provide a basics for intermodal associations which are important in individual recognition and social signalling systems in this species.     

Retinal projections in the bowfin, Amia calva: cytoarchitectonic and experimental analysis.

The retinofugal projections in the bowfin, a non-teleost actinopterygian, were studied by autoradiographic and horseradish peroxidase methods, and the cytoarchitecture of retinorecipient regions of the diencephalon was analyzed with serially sectioned, Bodian stained material. Nuclei were identified in the thalamus, the periventricular portion of the posterior tuberculum, synencephalon, and pretectum which are homologous to like-named nuclei in teleosts and other non-teleost actinopterygian fishes. Of particular note, a posterior pretectal nucleus and, possibly, a homologue of nucleus corticalis were found to be present in the pretectum. These nuclei have previously been identified only in teleosts. The posterior pretectal nucleus is relatively small in the bowfin, and the distribution of a small, versus a large, posterior pretectal nucleus in Teleostei and Halecomorphi suggests that this nucleus was small plesiomorphically. The pattern of retinofugal projections in the bowfin is similar to that in other non-teleost actinopterygian fishes and in teleosts in most regards. Contralaterally, the retina projects to nuclei in the dorsal and ventral thalamus, superficial and central pretectum, dorsal and ventral accessory optic nuclei, and to the optic tectum. Additionally, there are sparse projections to the suprachiasmatic nucleus in the preoptic area, the periventricular nucleus of the posterior tuberculum, and the dorsal and ventral periventricular pretectal nuclei. Ipsilateral projections are sparse and are derived from fibers which do not decussate in the optic chiasm. Undecussated ipsilateral retinal projections, as present in the bowfin, are a widely distributed character in vertebrates and appear to be plesiomorphic for vertebrates.     

The mormyrid mesencephalon. III. Retinal projections in a weakly electric fish, Gnathonemus petersii

The optic nerve and the retinal projections were studied in a mormyrid fish, Gnathonemus petersii, by using Fink-Heimer, HRP, cobalt labeling, and autoradiographic tracing techniques. The retinal fibers terminate bilaterally in the following places: suprachiasmatic nucleus, dorsolateral optic nucleus, optic nucleus of the posterior commissure, cortical nucleus, ventral pretectal area, optic tectum, and the accessory optic terminal field. The number of uncrossed fibers is relatively high in the suprachiasmatic nucleus, but negligibly small in the other retinal terminal fields. In the lateral geniculate nucleus and pretectal nucleus only crossed retinal fibers could be detected. The visual system of Gnathonemus is compared to that of other fishes, amphibians, and reptiles and the possible homologies are proposed. The comparison points to the conclusion that the visual system is less developed in Gnathonemus. This nocturnal species lives in turbid waters and has a special electric sense which may permit compensation for the reduced visual capacity.     

The morphology and connections of the posterior hypothalamus in the cynomolgus monkey (Macaca fascicularis). I. Cytoarchitectonic organization

The cytoarchitectonic organization of the posterior hypothalamus of the cynomolgus monkey (Macaca fascicularis) was analyzed in Nissl, Golgi, acetylcholinesterase, and reduced silver preparations. The region consists of a number of cell masses that differ considerably in their discreteness and in the homogeneity of their neuronal populations. The nuclei identified include: the medial mamillary nucleus (in which at least three distinct subdivisions can be recognized—a pars medialis, a pars lateralis, and a pars basalis); the small-celled nucleus intercalatus; the large-celled lateral mamillary nucleus; a single premamillary nucleus; the tuberomamillary nucleus; the posterior hypothalamic nucleus; the caudal extension of the lateral hypothalamic area; the supramamillary area; and the paramamillary nucleus (which appears to correspond to the nucleus of the nucleus of the ansa lenticularis of other workers). As a basis for the subsequent experimental study of the efferent connections of the posterior hypothalamus, the location of each of these cell masses is described and illustrated in a series of low-power photomicrographs, as are the form and distribution of the resident neuronal populations of the various components of themamillary complex as seen in Golgi preparations.     

Connections of the visual cortex in the hedgehog (Paraechinus hypomelas). II. Corticocortical projections

Cortical subdivisions based on cytoarchitectural and myeloarchitectural observations of normal tissue were correlated with the topography of corticocortical connections in the visual system of the Pakistani hedgehog. Large subpial aspiration lesions were made in both visual and non-visual cortical regions to determine the areal limits of the corticocortical connections of the visual cortex. Subsequently, discrete electrolytic lesions were placed within the visual cortex. After appropriate survival periods, the brains were processed and stained with the Fink-Heimer technique. The results of these studies show that the visual cortex may be subdivided into four distinct regions from lateral to medial; the lateral parastriate cortex, the lateral and medial part of striate cortex, and the medial parastriate cortex. Within these regions, interhemispheric connections between visual cortices arise mainly in the lateral striate and lateral parastriate regions and terminate in a single band within the lateral portion of the cytoarchitecturally defined striate cortex. These corticocortical projections, therefore, substantially overlap with the geniculostriate projections. Lateral striate cortex and lateral parastriate cortex project in a reciprocal fashion that correlates well with the physiologically defined mirror image representation of two retinotopic maps of the binocular visual field on cortex. These connections are reflected about a line that is closely correlated with the medial edge of the band of commissural axon terminals that is located within the lateral striate cortex, instead of corresponding exactly with the striate-parastriate border as they do in other mammals. Medial striate cortex projects to medial parastriate cortex, indicating that the monocular portion of V I is related to a separate secondary area of cortex on the medial wall of the hemisphere.     

Retinal projections in the cane toad, Bufo marinus.

The location and extent of retinorecipient areas in the cane toad, Bufo marinus, were established by anterograde transport of cobaltic-lysine complex from the cut optic nerve. Most of the labeled optic axons travelled in the marginal optic tract, while others were in the axial optic tract, and/or the basal optic tract. Retinal projections terminated in both contralateral and ipsilateral targets. In addition to the optic tectum, the main visual center, retinorecipient areas included the suprachiasmatic nucleus, rostral visual nucleus, neuropil of Bellonci, corpus geniculatum thalamicum, ventrolateral thalamic nucleus (dorsal part), posterior thalamic neuropil, uncinate neuropil, pretectal nucleus lentiformis mesencephali and basal optic nucleus. While all of these retinorecipient areas receive optic fibers from both eyes, the ipsilateral retinal projections were observed to be generally sparser than those from the contralateral retina. A sparse optic fiber projection covers the surface of the ipsilateral optic tectum and is most prominent rostromedially and caudolaterally. The position and the extent of each of the retinorecipient areas were determined in relation to a three-dimensional coordinate system. Morphometric analysis showed that 85.3% of the retinorecipient area is in the contralateral optic tectum, 10.4% in contralateral non-tectal areas, 1.6% in the ipsilateral optic tectum and 2.7% in ipsilateral non-tectal areas. The presence of an ipsilateral tectal projection and the well defined pretectal visual neuropil complex may be related to the highly developed visual behavior and visual acuity of Bufo marinus.     

Retinal projections in the native cat, Dasyurus viverrinus.

Retinal projections were examined in the native cat, Dasyurus viverrinus using Fink-Heimer material and autoradiography. We found six regions in the brain which receive retinal projections. These are (1) the dorsal lateral geniculate nucleus (2) the ventral lateral geniculate nucleus (3) the lateral posterior nucleus (4) the pretectum (5) the superior colliculus, and (6) the accessory optic system. We did not examine the hypothalamus. The accessory optic system and the lateral posterior nucleus receive a contralateral retinal projection only and the other four regions receive a bilateral retinal projection. There is extensive binocular overlap in the dorsal lateral geniculate nucleus. On the side contralateral to an eye injection of 3H leucine our autoradiographs show four contralateral layers which fill most of the nucleus. Three of these layers, 3, 4 and 5, also receive input from the opsilateral eye. Layer 1 which lies adjacent to the optic tract receives only contralateral retinal input. Layer 2 receives a direct retinal input only from the ipsilateral eye. The ipsilateral projection to the dorsal lateral geniculate nucleus forms a fairly continuous patch which is not divided into separate layers. The ipsilateral retinal input is located in the dorsal part of the lateral geniculate nucleus. The ventral quarter of the nucleus only receives a contralateral retinal input and therefore represents the monocular part of the visual field.     

Retinal projections in the Tasmanian devil, Sarcophilus harrisii.

Retinal projections were mapped in Tasmanian devils which had one eye injected with 3H-proline. The retinal fibers terminate in seven regions in the brain. These are (1) dorsal lateral geniculate nucleus (LGNd), (2) ventral lateral geniculate nucleus, (3) lateral posterior nucleus, (4) pretectum, (5) superior colliculus, (6) hypothalamus and (7) accessory optic system. The pattern of retinal input to six of these regions is similar to that seen in other marsupials. The pattern of retinal projections to the LGNd, while basically similar to that observed in other polyprotodont marsupials, is much simpler than that seen in the related native cat, Dasyurus viverrinus. The LGNd of Sarcophilus presents the simplest cytoarchitectural organisation of any marsupial examined so far. Each LGNd receives overlapping projections from both eyes. Suggestions of an intermittent lamination are seen in the LGNd contralateral to an eye injection of 3H-proline. On the ipsilateral side there are two patches of label, a large lateral patch and a smaller medial patch, both of which occupy areas receiving contralateral input. The monocular segment, occupying the ventral 40% of the nucleus, is more extensive than has been reported in any other polyprotodont marsupial.     

Cytoarchitectonic subdivisions of the dorsolateral frontal cortex of the marmoset monkey (Callithrix jacchus), and their projections to dorsal visual areas

We describe the organization of the dorsolateral frontal areas in marmoset monkeys using a combination of architectural methods (Nissl, cytochrome oxidase, and myelin stains) and injections of fluorescent tracers in extrastriate areas (the second visual area [V2], the dorsomedial and dorsoanterior areas [DM, DA], the middle temporal area and middle temporal crescent [MT, MTc], and the posterior parietal cortex [area 7]). Cytoarchitectural field 8 comprises three subdivisions: 8Av, 8Ad, and 8B. The ventrolateral subdivision, 8Av, forms the principal source of frontal projections to the "dorsal stream," having connections with each of the injected visual areas. The cytoarchitectural characteristics of 8Av suggest that this subdivision corresponds to the marmoset's frontal eye field. The intermediate subdivision of area 8 (8Ad) has efferent projections to area 7, while the dorsomedial subdivision (8B) has few or no connections with extrastriate cortex. Area 46, located rostrolateral to area 8Av, has substantial connections with the medial extrastriate areas (DM, DA, and area 7) and with MT, while the cortex lateral to 8Av (area 12/45) projects primarily to MT and to the MTc. The rostromedial prefrontal (area 9) and frontopolar (area 10) regions have very few extrastriate projections. Finally, cells in dorsal area 6 (6d) have sparse projections to DM, MT, and the MTc, as well as strong projections to DA and to area 7. These results illuminate aspects of the evolutionary development of the primate frontal cortex, and serve as a basis for further research into cognitive functions using a marmoset model.     

Systematic analysis of the visual projection neurons of Drosophila melanogaster. I. Lobula-specific pathways

In insects, visual information is processed in the optic lobe and conveyed to the central brain. Although neural circuits within the optic lobe have been studied extensively, relatively little is known about the connection between the optic lobe and the central brain. To understand how visual information is read by the neurons of the central brain, and what kind of centrifugal neurons send the control signal from the central brain to the optic lobe, we performed a systematic analysis of the visual projection neurons that connect the optic lobe and the central brain of Drosophila melanogaster. By screening approximately 4,000 GAL4 enhancer-trap strains we identified 44 pathways. The overall morphology and the direction of information of each pathway were investigated by expressing cytoplasmic and presynapsis-targeted fluorescent reporters. A canonical nomenclature system was introduced to describe the area of projection in the central brain. As the first part of a series of articles, we here describe 14 visual projection neurons arising specifically from the lobula. Eight pathways form columnar arborization in the lobula, whereas the remaining six form tangential or tree-like arborization. Eleven are centripetal pathways, among which nine terminate in the ventrolateral protocerebrum. Terminals of each columnar pathway form glomerulus-like structures in different areas of the ventrolateral protocerebrum. The posterior lateral protocerebrum and the optic tubercle were each contributed by a single centripetal pathway. Another pathway connects the lobula on each side of the brain. Two centrifugal pathways convey signals from the posterior lateral protocerebrum to the lobula.     

Retinal ganglion cells in normal hamsters and hamsters with novel retinal projections. I. Number,distribution, and size

We examined the number, spatial distribution, and size of ganglion cells in the retinae of normal Syrian hamsters and hamsters with retinal projections to the auditory and somatosensory nuclei of the thalamus, induced by neonatal surgery. As revealed by retrograde filling with horseradish peroxidase, there are about 64,600 contralaterally projecting retinal ganglion cells (RGCs) and 1,700 ipsilaterally projecting RGCs in the retinae of normal adult hamsters. Contralaterally projecting RGCs are distributed throughout the retina and have two local density peaks located within a central streak of high RGC density that is oriented approximately along the nasal-temporal axis. RGC density falls above and below the central streak, with a steeper gradient towards the upper retina. Ipsilaterally projecting RGCs are diffusely distributed within a crescent at the inferotemporal retinal periphery and are most dense at the internal border of the crescent. The soma diameter of contralaterally projecting RGCs ranges from 6 to 25 μm; the diameter distribution is unimodal, with a peak in the 10–13 μm range and is skewed toward smaller values, with an elongated tail towards higher values. Contralaterally projecting RGCs tend to be smaller in regions of higher density. Ipsilaterally projecting RGCs tend to be larger than contralaterally projecting RGCs both globally and within the temporal crescent, and their size distributions tend to be less regular and less well related to local density. The retinae of neonatally operated hamsters with novel retinal projections to the auditory and somatosensory systems contain about one-fourth the normal number of contralaterally projecting RGCs, whose relative density distribution is approximately normal despite the drastic reduction of absolute RGC density. The range and distribution of RGC soma diameters are similar in normal and neonatally operated hamsters, and, in operated as in normal hamsters, contralaterally projecting RGC somata tend to be smaller in regions of higher density. Our results in normal hamsters suggest a role for intraretinal mechanisms in the determination of RGC size. Our findings in neonatally operated hamsters suggest that, despite the reduced number of RGCs in these animals, the same types of RGCs are found in the retinae of normal and neonatally operated hamsters. © 1995 Wiley-Liss, Inc.     

Postnatal development of primary visual projections in the tammar wallaby (Macropus eugenii)

The time course and pattern of retinal innervation of primary visual areas was traced in pouch-young wallabies. Tritiated proline was injected into one eye of animals ranging in age from 1 to 72 days after birth. These results are compared to the 11 primary visual areas found in the adult wallaby, seven of which receive binocular input while four are monocular. At birth retinal ganglion cell axons have not reached any visual areas. Two to 4 days after birth, all of the axons are crossing to the contralateral optic tract. Nine to 12 days after birth axons begin to invade the contralateral lateral geniculate nucleus, the superior colliculus, and the medial terminal nucleus. Twenty to 21 days after birth, ipsilateral axons invade the lateral geniculate nucleus and superior colliculus. The contralateral projection precedes the ipsilateral projection in all binocular visual areas. By 25 days, ipsilateral and contralateral afferents share common territory in the lateral geniculate nucleus; however, afferents from each eye are initially concentrated in appropriate areas. Between 52 and 72 days, afferents to the dorsal lateral geniculate nucleus are gradually segregated into nine terminal bands. Four are contralateral while five are ipsilateral. By 72 days, the ipsilateral component to the superior colliculus is clustered beneath the contralateral projection a deeper layer. Projections to four monocular visual areas--lateral posterior nucleus, dorsal terminal nucleus, lateral terminal nucleus, and nucleus of the optic tract--are established later than binocular visual areas, except the suprachiasmatic nucleus. The suprachiasmatic nucleus is the last to be bilaterally innervated even though it is situated closest to the optic chiasm. At the light microscope level a mature pattern of visual development is emerging by 72 days, although the eyes do not open until 140 days.     

Cortical and subcortical projections to primary visual cortex in anophthalmic,enucleated and sighted mice

The purpose of this study was to identify and compare the afferent projections to the primary visual cortex in intact and enucleated C57BL/6 mice and in ZRDCT/An anophthalmic mice. Early loss of sensory‐driven activity in blind subjects can lead to activations of the primary visual cortex by haptic or auditory stimuli. This intermodal activation following the onset of blindness is believed to arise through either unmasking of already present cortical connections, sprouting of novel cortical connections or enhancement of intermodal cortical connections. Studies in humans have similarly demonstrated heteromodal activation of visual cortex following relatively short periods of blindfolding. This suggests that the primary visual cortex in normal sighted subjects receives afferents, either from multisensory association cortices or from primary sensory cortices dedicated to other modalities. Here cortical afferents to the primary visual cortex were investigated to determine whether the visual cortex receives sensory input from other modalities, and whether differences exist in the quantity and/or the structure of projections found in sighted, enucleated and anophthalmic mice. This study demonstrates extensive direct connections between the primary visual cortex and auditory and somatosensory areas, as well as with motor and association cortices in all three animal groups. This suggests that information from different sensory modalities can be integrated at early cortical stages and that visual cortex activations following visual deprivations can partly be explained by already present intermodal corticocortical connections.     

Corticobulbar projections of the marsupial phalanger (Trichosurus vulpecula). I. Projections to the pons and medulla oblongata

A total of 27 adult phalangers was employed to investigate the pattern of neocortical projections to the pontine and medullary portions of the brain stem. Lesions restricted to neocortical areas rostral to the orbital sulcus resulted in fiber degeneration which distributed mainly to midline and medial areas of the pontine and medullary reticular formation. The greatest amount of fiber degeneration was located within the superior central nucleus, the nucleus of the pontine raphe, the nucleus pontis centralis oralis and the nucleus pontis centralis caudalis. However, a few degenerating fibers were present within the nucleus gigantocellularis and the magnocellular portion of the medullary raphe. In contrast, lesions which were located just caudal to the orbital sulcus resulted in fiber degeneration chiefly within the more lateral parvocellular reticular formation and within the subnucleus dorsalis of the nucleus medullae oblongatae centralis. In such cases, additional degenerating fibers were present within the dorsal column nuclei and within more medial areas of the reticular formation. In those brains with ventral parietal ablations, degenerating fibers were present within the chief sensory and spinal nuclei of the trigeminal complex and the closely adjacent reticular formation. All of the above neocortical lesions resulted in fiber degeneration within the basilar pontine gray. In those specimens subjected to caudal (striate and peristriate) or ventrocaudal (temporal) lesions, degenerating fibers were present within the basilar pontine gray, but not within other areas of the pons or the medulla oblongata.     

Retinal projections and retinal ganglion cell distribution patterns in a sturgeon (Acipenser transmontanus), a non-teleost actinopterygian fish

Retinal projections in a sturgeon were studied by injecting biocytin or HRP into the optic nerve. The target areas are the preoptic area, thalamus, area pretectalis, nucleus of posterior commissure, optic tectum, and nuclei of the accessory optic tract. Furthermore, a few labeled fibers and terminals were found in a ventrolateral area of the caudal telencephalon. All retinal projections are bilateral, although contralateral projections were more heavily labeled. Retrogradely labeled neurons were found in the ventral thalamus bilaterally. Retinal projections in sturgeons are similar to those of other non-teleost actinopterygians and chondrichthyans (sharks), in terms of the targets and extent of bilateral projections. Distribution patterns of ganglion cells in the retina were examined in Nissl-stained retinal whole mount preparations. The highest density areas were found in the temporal and nasal retinas, and a dense band of ganglion cells was observed along the horizontal axis between the nasal and temporal areas of highest density. The density of ganglion cells in the dorsal retina is the lowest. The total number of ganglion cells was estimated to be about 5 x 10(4) in a retina. The existence of a low density area in the dorsal retina suggests reduced visual acuity in the ventral visual field.