Morphology,axonal projection pattern,and responses to optic nerve stimulation of thalamic neurons in the fire-bellied toad Bombina orientalis

Intracellular recording and biocytin labeling were carried out in the fire-bellied toad Bombina orientalis to study the morphology and axonal projections of thalamic (TH) neurons and their responses to electrical optic nerve stimulation. Labeled neurons (n = 142) were divided into the following groups: TH1 neurons projecting to the dorsal striatum; TH2 neurons projecting to the amygdala, nucleus accumbens, and septal nuclei; TH3 neurons projecting to the medial or dorsal pallium; TH4 neurons with projections ascending to the dorsal striatum or ventral striatum/amygdala and descending to the optic tectum, tegmentum, and rostral medulla oblongata; TH5 neurons with projections to the tegmentum, rostral medulla oblongata, prectectum, or tectum; and TH6 neurons projecting to the hypothalamus. TH1 neurons are found in the central, TH2 neurons in the anterior and central, TH3 neurons in the anterior dorsal nucleus, and TH4 and TH5 neurons in the posterior dorsal or ventral nucleus. Neurons with descending projections arborize in restricted parts of retinal afferents; neurons with ascending projections do not substantially arborize within retinal afferents. At electrical optic nerve stimulation, neurons in the ventral thalamus respond with excitation at latencies of 10.8 msec; one-third of them follow repetitive stimulation and possibly are monosynaptically driven. Neurons in the dorsal thalamus respond mostly with inhibition at latencies of 42.3 msec and are polysynaptically driven. This corroborates the view that neurons in the dorsal thalamus projecting to the telencephalon receive no substantial direct retinal input and that the thalamopallial pathway of amphibians is not homologous to the mammalian retinogeniculocortical pathway.     

Morphology,axonal projection pattern,and response types of tectal neurons in plethodontid salamanders. II: Intracellular recording and labeling experiments

In the plethodontid salamanders Plethodon jordani and P. glutinosus, the morphology and axonal projections of 140 tectal neurons and their responses to electrical optic nerve stimulation were determined by intracellular recording and biocytin labeling. Six types of neurons are distinguished morphologically. TO1 neurons have wide dendritic trees that arborize mainly in tectal layers 1 and 3; they project bilaterally to the tegmentum and contralaterally to the medulla oblongata. TO2 neurons have very wide dendritic trees that arborize mainly in layers 2 and 3; axons project bilaterally or unilaterally to the pretectum and thalamus and ipsilaterally to the medulla oblongata. TO3 neurons have very wide and flat dendritic trees confined to layers 3–5; some have the same axonal projection as TO2 neurons, whereas others have descending axons that reach only the level of the cerebellum. TO4 neurons have narrower dendritic trees that arborize in layers 2 and 3; they project to the ipsilateral pretectum, thalamus, and medulla oblongata. TO5 neurons have dendritic trees that arborize in layers 1 and 2 or 1–3 and project bilaterally or unilaterally to the pretectum and thalamus. TO-IN are interneurons, with a number of subtypes with respect to variations in dendritic arborization pattern. TO1–TO5 neurons generally have short latencies of 2–16 ms (average = 8.4 ms) at electrical optic nerve stimulation; first responses are always excitatory, often followed by inhibition. They are likely to be mono- or oligosynaptically driven by retinal afferents. TO-IN interneurons have long latencies of 20–80 ms (average = 38.6 ms) and appear to receive no direct retinal input. With their specific dendritic arborization, consequent dominant retinal input, specific axonal projections, the different types of tectal projection neurons constitute separate ascending and descending visual pathways. Hypotheses are presented regarding the nature of the information processed by these pathways. J. Comp. Neurol. 404:489–504, 1999. © 1999 Wiley-Liss, Inc.     

Tectal fiber connections in a non-teleost actinopterygian fish, the sturgeon Acipenser

Tectal fiber connections were studied in members of an early branch of the actinopterygian lineage, the sturgeons Acipenser transmontanus and A. schrenkii, by means of biocytin, HRP, biotinylated dextran amine, and DiI tract tracing methods. The aim of this study is to elucidate the visual pathway via the optic tectum to the thalamus as a part of a series of studies on the visual pathways in sturgeons. After biocytin or biotinylated dextran amine injections to the optic tectum terminals are found bilaterally in the medial and lateral portions of both the dorsal thalamus and ventral thalamus. Ipsilateral projections are much more abundant. Tectal recipient areas in the thalamus overlap in part with the retinal recipient areas. After HRP or DiI injections to the dorsal or ventral thalamus, tectal neurons projecting to the thalamus were labeled in the ipsilateral or bilateral stratum periventriculare. Dendritic morphology of tectothalamic neurons suggests that they receive direct retinal input. These results suggest that visual information passes through the tectum to the thalamic areas which also receive direct retinal projections. In this regard, the visual system of Acipenser resembles that of chondrichthyans (sharks). Other fiber connections of the tectum are also described, which have not previously been studied by tracer methods in a sturgeon.     

Retinal projections in the australian lungfish

Autoradiographic analysis of the primary retinofugal projections in the Australian lungfish reveals contralateral retinal projections to a ventral portion of the periventricular preoptic nucleus, throughout its rostrocaudal extent, and to 4 distinct terminal fields in the thalamus. Only one of these thalamic fields (t4) likely receives dendrites soley from dorsal thalamic neurons. Thalamic terminal field 1 probably receives dendrites from both dorsal and ventral thalamic neurons, and fields 2 and 3 from only ventral thalamic neurons. Contralateral retinofugal fibers terminate in the pretectum and in the superficial and central tectal zones. The central tectal terminal field is restricted to the medial one-third of the tectum. At pretectal levels a contralateral basal optic tract arises from the marginal optic tract and terminates along the lateral edge of the tegmentum, as a series of glomerular puffs, and in the rostral pole of a superficial isthmal nucleus. The Australian lungfish, unlike the African and South American lungfish, possesses ipsilateral retinal projections to all of the nuclei that receive contralateral retinal input.     

Retinofugal and retinopetal projections in the green sunfish, Lepomis cyanellus

The retinofugal and retinopetal connections in the green sunfish were studied by autoradiographic and horseradish peroxidase methods. All retinofugal fibers decussate in the optic chiasm. Some fibers project to contralateral preoptic and hypothalamic nuclei while others recross to project to the comparable ipsilateral nuclei. Contralaterally, the medial optic tract projects to the periventricular thalamic and pretectal nuclei and, sparsely, to the rostral optic tectum. The dorsal optic tract projects to the parvocellular portion of the superficial pretectal nucleus, the central pretectal nucleus, nucleus corticalis, and the rostral portion of the optic tectum. The ventral optic tract primarily projects to the caudal portion of the optic tectum, giving off fibers in route to innervate various nuclei, including the parvocellular superficial pretectal nucleus and the dorsal and ventral accessory optic nuclei. The axial optic tract projects to the dorsal accessory optic nucleus, the central pretectal nucleus, and the caudal optic tectum. Retinal fibers reach the ipsilateral thalamus, pretectum and other sites via a redecussation through the posterior commissure. From outgroup analysis it is concluded that such redecussating fibers are an independently derived character within actinopterygians and are homoplasous to nondecussating ipsilateral retinal projections in other vertebrates. Neurons retrogradely labeled with horseradish peroxidase were found to form a rostrocaudal column from the olfactory bulb and nerve through the ventral telencephalon to caudal diencephalic levels along the medial aspect of the optic tract. It is possible that all these neurons consist of one population of migrated ganglion cells of the nervus terminalis.     

Retinal projections in lamprey (Lampetra fluviatilis)

Visual projections in lamprey were investigated using two methods,--one by revealing transport of horseradish peroxidase, and the other by silver impregnation of degenerating axons and terminals after enucleation of the eye. Both methods produced similar results. The chiasm showed incomplete crossing of retinal fibres, the major part of which, as an optic tract, proceed along the contralateral thalamus up to the entry into the optic tectum, while the smaller part takes the same course on the ipsilateral side. Besides, from the posterior part of the optic chiasm an axial optic tract branches off, which proceeds through the central part of the contralateral thalamus up to the pretectal nucleus, individual fibres of which enter the central grey layer of the optic tectum. On the contralateral side, the visual projections are localized in the lateral geniculate body, pretectal nucleus, in the three upper layers of the optic tectum, in the ventrolateral area of the optic tectum and as solitary diffuse projections in the mesencephalic tegmentum. Innervation of thalamic and pretectal nuclei are realized by two tracts--the tractus opticus proper, and tractus opticus axialis. On the ipsilateral side visual projections, excepting the optic tract, are scarce and in the thalamus appear as small areas of the lateral geniculate body and pretectum adjacent to the optic tract. Solitary visual projections were found in two upper layers of the rostral optic tectum and in larger numbers in the 3rd and 4th layers of the caudal part and in ventrolateral area of the optic tectum. Projections in mesencephalic tegmentum were single. Diffuse visual projections in the lateral part of hypothalamus could be revealed only by the silver impregnation method. Using the peroxidase method two types of cells were observed in mesencephalic tegmentum where, possibly, the centrifugal fibres proceeding to retina, originate. A comparison is made of central visual projections in lampreys and other representatives of nonmammalian vertebrates.     

Retinal projections in larval,transforming and adult sea lamprey,Petromyzon marinus

Unilateral enucleations were performed on larval, transforming and adult sea lampreys. Following 5 to 11 days survival, the animals were sacrificed and the brains were processed using a modified Fink-Heimer technique. In larvae, contralateral optic projections were found to the posterior one-third of the dorsal thalamus, the pretectum, and the optic tectum. No ipsilateral projections were present in the larvae. In enucleated transforming and adult lampreys, degenerating axons were observed in the optic chiasm and bilaterally in the optic tracts. Retinal efferents projected bilaterally to a lateral neuropil region (“tractus opticus”) in the posterior one-half of the dorsal thalamus. Contralaterally, a conspicuous dorsomedial cell group (lateral geniculate nucleus) also received a projection. Contralateral projections to the superficial layers of the pretectum and optic tectum were observed. Ipsilateral retinal projections to the pretectum and optic tectum in transforming and adult lampreys were restricted to a small zone at the ventrolateral margins of the pretectum and tectum. The changes in distribution of retinofugal projections during transformation appear to be occurring at the same time that the eye differentiates into its adult form.     

Tectal efferents in the banded water snake,Natrix sipedon

Visual information reaches the dorsal thalamus by two distinct routes in most reptiles. Retinal efferents terminate directly in the dorsal lateral geniculate nucleus (DLGN). Retinal information is also channeled indirectly through the tectum to nucleus rotundus. Retinal projections to DLGN and tectum are also well esablished in snakes, but the status of the tecto-rotundal link of the indirect visual pathway is uncertain. Thus, tectal efferents were studied with Fink-Heimer methods in banded water snakes (Natrix sipedon). The tectum gives rise to crossed and uncrossed projections to the brainstem reticular formation. Commissural connections are effected with the contralateral tectum via the tectal and osterior commissures. tectum projects densely to the ipsilateral basal optic nucleus. Bilateral ascending projections reach the pretectal area, nucleus lentiformis mesencephali, lateral habenular nuclei, and posterodorsal nuclei. Ascending projections reach the ventral lateral geniculate and suprapeduncular nuclei. there is a diffuse projection to the central part of the caudal thalamus and a dense, bilaternal projection to the DLGN. These results indicate that the relation of the tectum to the dorsal thalamus is different in snakes than in other reptiles. Nucleus rotundus is either absent or poorly differentiated and there is a strong convergence of the direct and indirect visual pathways at DLGN.     

Single-unit study of lateral line cells in the optic tectum of Xenopus laevis: evidence for bimodal lateral line/optic units

Responses of single units in the Xenopus tectum to stimulation of the contralateral anterior lateral line nerve (cALLN) and optic nerve were studied. Cells responded to cALLN stimulation with a phasic burst of spikes that was repeatable between trials; latencies ranged from 4 to 23 msec. The most excitable cells were located in layer 6 of the ventrolateral tectum. Cells responding to stimulation of the ipsilateral ALLN were far less numerous and robust, and showed latencies 3-10 msec greater than those of contralateral responses. Tectal cell responses to cALLN nerve stimulation grew progressively to saturation with stimulus voltage and paralleled the growth of the ALLN compound action potential; cells responded to stimulation of either supra- or infraorbital branches of cALLN. These observations indicate convergence of primary lateral line afferents in the medulla and/or tectum. Lateral line tectal cells showed strong habituation at interstimulus times less than 8-20 seconds. Experiments on bimodal cells revealed facilitatory and inhibitory interactions between optic and lateral line inputs. Some cells responded to stimulation of either lateral line or optic nerves, with combined stimulation producing responses exceeding the sum of responses to separate nerve stimulation. In other cells the response to optic nerve stimulation was markedly increased by lateral line nerve stimulation, despite the absence of response to lateral line nerve stimulation alone. Facilitation was also evident in cells that responded only to combined stimulation of lateral line and optic nerves. Some cells exhibited an early (5-10 msec) and late (20-40 msec) response to optic nerve stimulation; lateral line nerve stimulation, despite eliciting no response itself, produced strong facilitation of the early but almost complete suppression of the late optic nerve response.     

Central pathway of the extraocular muscle proprioception

In a first group of acute experiments in lambs, the cellular pool of the trigeminal ganglion which innervates the eye muscle spindles was electrophysiologically individuated and then stimulated with single shocks. Evoked potentials could be recorded from some ipsilateral mesodiencephalic sites (tectum, tegmentum, medial lemniscus, posteroventromedial nuclei) which responded also to the manual stretch of the ipsilateral extraocular muscles. The latencies of the onset of the responses ranged from 1 to 5 msec. In chronic experiments in lambs, the pontine representation of the eye muscle proprioception was electrophysiologically identified in the oral part of ipsilateral descending trigeminal nucleus and then destroyed by means of a discrete electrolysis. The animals were killed after 8–13 days. Histological examination showed degenerated nerve fibers along the medial lemniscus and the dorsal trigemino-thalamic tract. All degeneration was ipsilateral and terminated in the posteroventrolateral and posteroventromedial nuclei of the thalamus. The results of the present investigations confirm the previous assumption that the oral part of the descending trigeminal nucleus contains the perikarya of the second-order neurons of the eye muscle proprioceptors whose axons reach the mesodiencephalic regions through the medial lemniscus and the dorsal trigeminothalamic tract.     

The diencephalon of the pacific herring,Clupea harengus: Retinofugal projections to the diencephalon and optic tectum

The pattern of retinofugal projections to nuclei in the diencephalon and to the optic tectum was analyzed with horseradish peroxidase and autoradiographic methods in Clupea harengus, a clupeomorph teleost, for comparison with osteoglossomorph, elopomorph, and euteleost teleosts and with non-teleost actinopterygians. Most retinal fibers decussate in the optic chiasm and project to nuclei in the preoptic area, ventral and dorsal thalamus, posterior tuberculum, synencephalon, and pretectum, as well as to the accessory optic nuclei and optic tectum. Some ipsilateral projections do not decussate in the optic chiasm, while others decussate and recross via the supraoptic (minor) and posterior commissures. The pattern of projections is similar to that seen in other actinopterygian fishes with several exceptions. The terminal field usually present lateral to nucleus anterior in the dorsal thalamus is extremely reduced despite the relatively large size of the nucleus. A dense terminal field lies within the cell plate of nucleus corticalis in the pretectum rather than dorsal to it. The tectal hemisphere is composed of two distinct lobules, and the dorsal optic tract projects to the more rostromedial lobule while the ventral optic tract projects to the more caudolateral lobule. The lack of a significant projection to nucleus anterior and the lobular morphology of the optic tectum appear to be apomorphic for Clupea. Other features of the pattern of retinal projections are also analyzed in actinopterygian fishes including Clupea, and several hypotheses are advanced as to which traits are plesiomorphic for actinopterygians and/or for teleosts. © 1993 Wiley-Liss, Inc.     

Afferent and efferent connections of the torus semicircularis in the sea lamprey: an experimental study

The afferent and efferent connections of the torus semicircularis (TS) of larval sea lampreys were studied with horseradish peroxidase, carbocyanine dye (DiI) and fluorescein-coupled or Texas-Red-coupled dextran amine tract-tracing methods. Application of tracers to the TS or to the octavolateral area revealed the presence of bilateral projections from the octavolateral area to the torus semicircularis, mainly from the mechanoreceptive regions (medial and ventral octavolateral nuclei) though also from the electroreceptive (dorsal octavolateral nucleus) region. The nucleus of the descending root of the trigeminal nerve projects to the contralateral TS, mostly from neurons located rostral to the obex. Fairly numerous reticular cells of the rhombencephalon project to the torus semicircularis. In the mesencephalon, scattered cells in the tegmentum, and some in the tectum, have toral projections, mostly ipsilateral. Numerous thalamic neurons, as well as fairly numerous neurons of the posterior tubercle, hypothalamus and preoptic region, and a few neurons in the ventral telencephalon (striatum, septum), were labeled after tracer application to the TS. The torus semicircularis mainly projects to the thalamus, the hypothalamus and the reticular rhombencephalic nuclei. Our results reveal for the first time a complex pattern of connections of the lamprey TS, which suggests that it is a multisensory center integrating head cutaneous sensitivity with mechano- and electrosensory information from the octavolateral area and with visual information. A number of afferents from the forebrain also appear to contribute to TS function.     

Connections of the tectum opticum in two urodeles, Salamandra salamandra and Bolitoglossa subpalmata, with special reference to the nucleus isthmi

Tectal connections were studied in two urodele species following horseradish peroxidase injections into the tectum opticum. In both species retrogradely labelled cells were observed: ipsilaterally in the corpus striatum, lateral amygdala, ventral and dorsal thalamus and nucleus of DARKSCHEWITSCH--bilaterally in the pretectal nucleus, dorsal tegmentum and nucleus reticularis medius--contralaterally in the tectum opticum and area octavo lateralis. Besides these nuclei the nucleus isthmi was bilaterally labelled. Rostral efferent projections of the tectum opticum terminated in the ipsilateral pretectal area and the ipsilateral dorsal and ventral thalamus ipsilaterally coursing to the contralateral tectum via the commissura postoptica. Caudal efferents formed the bilaterally organized tecto-bulbar tracts innervating the rhombencephalon. Comparison of the results of a series of tectal horseradish peroxidase injections differing in depth, tangential extension and location, indicated that tectal afferents from the telencephalon, the contralateral tectum opticum and the medulla were sparse and widely branching. Projections of the telencephalon and all diencephalic nuclei terminated deep in the rostral tectum opticum. Projections of the medulla terminated preferentially deep in the caudal tectum opticum. The tecto-isthmic projection was highly topographic forming a layered terminal field lateral to the nucleus isthmi. The isthmo-tectal projection innervated the whole tectum opticum on the ipsilateral side and was highly topographic. On the contralateral side the caudal part of the tectum opticum was not innervated. The isthmo-tectal fibers terminated superficially in the tectum opticum on both sides of the brain. The nucleus isthmi identified here is proposed to be homologe to that of other vertebrates.     

Physiological Characterization of Pretectal Neurons Projecting to the Láteral Geniculate Nucleus in the Cat

Single neurons in the pretectal nucleus of the optic tract and posterior pretectal nucleus were extracellularly recorded in anaesthetized cats and tested for antidromic activation after electrical stimulation of the ipsilateral dorsal lateral geniculate nucleus. Cells were further characterized by their response latencies to electrical stimulation of the optic nerve head and the optic chiasm, and by responses to various visual stimuli. 46 out of 188 neurons (24%) were antidromically activated from the lateral geniculate nucleus at response latencies of 0.6 - 2.6 ms. They had low spontaneous activities and preferred fast-moving visual stimuli. 29 of the antidromically activated neurons (63%) could be activated from the optic chiasm with response latencies of 4–10 ms. Together with the mean conduction time of 0.8 ms between the optic nerve head and the optic chiasm, this indicates that they receive an indirect retinal input via fast-conducting Y-fibres. Sometimes antidromically activated neurons spontaneously showed irregular burst activity. During unidirectional stimulation with a large moving visual stimulus, burst activity became more regular, and interburst intervals and the duration of single bursts decreased. After the stimulus was stopped, interburst intervals slowly increased until prestimulation activity was restored. The response properties of these neurons could reflect the transfer of saccade-related visual as well as oculomotor signals through the pretectum to the visual thalamus.     

Wulst efferents in the little owl Athene noctua: an investigation of projections to the optic tectum.

The efferent projections from the Wulst were studied in the little owl, Athene noctua, using anterograde migration of wheat-germ-agglutinin conjugated horseradish peroxidase (WGA-HRP). Wulst projections were distributed to telencephalic, diencephalic and mesencephalic targets in a general pattern similar to that previously described in other avian species. Our results on the organization of the Wulst-optic tectum pathway in the little owl reveal well defined and laminarly arranged terminal projections into the superficial tectal layers, with a distribution suggestive of topographical relationships between neurons of origin in the Wulst and termination fields in the optic tectum. In contrast to lateral-eyed birds, the little owl possesses conspicuous contralateral projections to the optic tectum. Ipsilateral and contralateral efferents are restricted to different tectal regions, i.e. ipsilateral projections to the caudo-dorsal and contralateral projections to the rostro-ventral optic tectum. In addition, the anterior and posterior Wulst differentially contribute to the ipsilateral and contralateral projections to the optic tectum. This differential organization of Wulst efferents, as well as the presence of substantial contralateral projections, might be related to the high degree of binocular overlap typical of frontal-eyed birds. At a functional level, electric potentials recorded in the optic tectum and evoked by visual stimulation showed that information from one eye can reach the ipsilateral optic tectum. After Wulst ablation, the amplitude of these potentials was significantly reduced, indicating that Wulst efferents may influence visually-evoked activity in the optic tectum.     

Monocular and binocular optic inputs to salamander pretectal neurons: intracellular recording and HRP labelling study

Intracellular recordings and horseradish peroxidase injections were performed in the pretectum and adjacent tegmentum of Salamandra salamandra, while both optic nerves were electrically stimulated. In approximately half of the recorded units no spikes could be evoked but rather graded postsynaptic potentials. The latter type morphologically showed features of interneurons. From a total of 48 recorded units, nearly 60% were excited only by the contralateral optic nerve, whereas approximately 40% were binocular. For the most part (10/19) the binocular cells were excited by the contralateral and inhibited by the ipsilateral optic nerve. Fewer neurons (7/19) received excitatory inputs from both optic nerves. The latency distribution of the monocular cells shows a maximum of 20-30 ms. The same maximum exists for the contralateral inputs to the binocular cells, whereas the ipsilateral inputs to these units were nearly as frequent with latencies of 20-30 and 40-50 ms. Since neurons with the short ipsilateral latencies always had parts of their dendrites within the ipsilateral ocular projection field, a feature which was lacking in the cells with long ipsilateral latencies, it is possible that the longer latencies are due to indirect ipsilateral inputs. Efferents of labelled dorsal pretectal cells reach the contralateral pretectum via the posterior commissure, the basal optic neuropil of the accessory optic system and the tegmental white substance. More ventrally located cells often reach the pretectal and the basal optic neuropil with their dendrites. Axons of this type descend to the medulla oblongata via the medial longitudinal fasciculus.     

Light experience and lateralization of the two visual pathways in the chick

Using retrograde labelling with the fluorescent tracer rhodamine B isocyanate (RITC), we have examined the organisation of the thalamofugal and tectofugal visual projections to the forebrain of the young chick. In addition, we have investigated the influence of light exposure prior to hatching on the development of the tectofugal visual projections. Our results for the thalamofugal projections confirm those found previously; viz., that there are more projections from the left side of the thalamus to the right hyperstriatum of the forebrain than from the right side of the thalamus to the left hyperstriatum in males and females. The organisation of the tectofugal visual projections to the rotundal nuclei was more symmetrical (males only examined) although there was a trend towards a greater number of projections from the left optic tectum to its ipsilateral nucleus rotundus than from the right optic tectum to its ipsilateral nucleus rotundus. There are numerous projections from the optic tecta to their contralateral rotundal nuclei but, in contrast to reports for the pigeon, no marked asymmetry was present in these. The ratio of contralateral to ipsilateral projections revealed significant asymmetry for projections from the ventral regions of the optic tecta and symmetry from the dorsal regions. Thus both visual pathways of the chick have asymmetrical organisation but the asymmetry is much greater in the thalamofugal pathway. The slight asymmetry in the tectofugal projections may be determined by exposing the embryo to light just before hatching, as known to be the case for thalamofugal projections.     

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.     

Labelled neurons in mesencephalon and medulla oblongata of newt after periocular injection of horseradish peroxidase

The retrograde transport of HRP after periocular space injection was investigated in mesencephalon and medulla oblongata of newt brain. In the tegmentum the neurons of oculomotor and troclear nucleus are filled. In the optic tectum some filled cells of mesencephalic trigeminal nucleus were, for the first time, described. This suggest that these neurons are deputated to proprioceptive innervation of the extrinsic ocular muscles. In the medulla oblongata the labelled neurons were located in the ganglion of Gasser and in the sensitive column of the trigeminal area. Other labelled neurons were found in the abducent nucleus and in the visceromotor column of the facial nerve. The authors discuss the analogy between the trigeminal labelled neurons of the medulla oblongata with supratrigeminal nucleus of the mammals.