Synaptology of the medullary command (pacemaker) nucleus of the weakly electric fish (Apteronotus leptorhynchus) with particular reference to comparative aspects

Summary The general organization and synaptology of the medullary command (pacemaker) nucleus (MCN) was investigated in the high frequency weakly electric fish, Apteronotus leptorhynchus. This study was undertaken in order to establish differences and similarities between the MCN of A. leptorhynchus and that of the closely related species, Apteronotus albifrons which has been studied previously. The basic morphology and synaptology of the MCN in A. leptorhynchus is similar to that of A. albifrons. The MCN of A. leptorhynchus consists of large (relay) and small (pacemaker) cells; both cell types receive synaptic input or large club endings with electrotonic gap junctions and bouton-like terminals with polarized chemical synapses. Club endings originate from thick meyelinated fibres belonging to the small (pacemaker) cells, whereas the bouton-like terminals issue from thin myelinated fibers of extranuclear origin. Via their club endings, the small (pacemaker) cells are connected both to each other and to the large (relay) cells. Besides the similarities, there are distinct and characteristic differences between the MCN of the two species, which mainly concern the synaptology of the nucleus. In A. leptorhynchus, the large (relay) cells possess long dendritic processes, covered exclusively with bouton-like terminals; the axon initial segment of large (relay) cells receives boutons, in addition to club endings. Small (pacemaker) cells have short dendritic protrusions receiving input from club endings and boutons; furthermore, the small pacemaker cells axon initial segment receives both club endings and bouton-like terminals. These differences are discussed in terms of the functional organization of the MCN in certain gymnotoids and draw attention to the fact that the morphological and ultrastructural aspects of the central command of the electric organ discharge reveal several differences not only between different gymnotoid fish (Apteronotus and Eigenmannia) but also between closely related species such as A. albifrons and A. leptorhynchus.     

Retinofugal projections in a weakly electric gymnotid fish (Apteronotus leptorhynchus)

The eyes of weakly electric gymnotid fish are poorly developed in comparison to those of most diurnal teleosts. The tectum and pretectum, despite their usual association with the visual system, are large and well differentiated in gymnotids. We have studied retinal projections in gymnotids in order to define the visual components of the mesencephalon and diencephalon and thus allow comparison with other teleosts in which retinofugal fibers have been extensively mapped. Retinofugal projections reported in this work are based on the anterograde transport of conjugated wheat germ agglutinin horseradish peroxidase, following injection into the posterior chamber of the eye of Apteronotus leptorhynchus (brown ghost knife fish). The results show a remarkable similarity to those of non-electroreceptive teleosts. Although the optic nerves appear to cross completely at the optic chiasm, close scrutiny shows a slender recrossing fascicle which continues from the contralateral tractus opticus medialis through the rostroventral hypothalamus to reach the ipsilateral side, providing a scanty projection to the n. opticus hypothalamicus, n. anterior periventricularis, n. dorsolateralis thalami, and n. commissurae posterioris. A few fibers ascend via the tractus opticus dorsomedialis to the rostral dorsomedial part of the stratum fibrosum et griseum superficiale of the ipsilateral tectum. The main body of the retinal projections in Apteronotus are to the following contralateral target areas: preoptic area, n. opticus hypothalamicus, n. anterior periventricularis, n. dorsolateralis thalami, n. pretectalis, area pretectalis, n. corticalis, n. commissurae posterioris, n. geniculatus lateralis, area and n. ventrolateralis thalami, caudal dorsal tegmentum and the tectum opticum. The retinotectal projection is modest in comparison to that of more vision dependent fish and terminates mainly in the upper half of the stratum fibrosum et griseum superficiale; hardly any retinal fibers reach the caudalmost tectum.     

Precision of the pacemaker nucleus in a weakly electric fish: network versus cellular influences

We investigated the relative influence of cellular and network properties on the extreme spike timing precision observed in the medullary pacemaker nucleus (Pn) of the weakly electric fish Apteronotus leptorhynchus. Of all known biological rhythms, the electric organ discharge of this and related species is the most temporally precise, with a coefficient of variation (CV = standard deviation/mean period) of 2 x 10(-4) and standard deviation (SD) of 0.12-1.0 micros. The timing of the electric organ discharge is commanded by neurons of the Pn, individual cells of which we show in an in vitro preparation to have only a slightly lesser degree of precision. Among the 100-150 Pn neurons, dye injection into a pacemaker cell resulted in dye coupling in one to five other pacemaker cells and one to three relay cells, consistent with previous results. Relay cell fills, however, showed profuse dendrites and contacts never seen before: relay cell dendrites dye-coupled to one to seven pacemaker and one to seven relay cells. Moderate (0.1-10 nA) intracellular current injection had no effect on a neuron's spiking period, and only slightly modulated its spike amplitude, but could reset the spike phase. In contrast, massive hyperpolarizing current injections (15-25 nA) could force the cell to skip spikes. The relative timing of subthreshold and full spikes suggested that at least some pacemaker cells are likely to be intrinsic oscillators. The relative amplitudes of the subthreshold and full spikes gave a lower bound to the gap junctional coupling coefficient of 0.01-0.08. Three drugs, called gap junction blockers for their mode of action in other preparations, caused immediate and substantial reduction in frequency, altered the phase lag between pairs of neurons, and later caused the spike amplitude to drop, without altering the spike timing precision. Thus we conclude that the high precision of the normal Pn rhythm does not require maximal gap junction conductances between neurons that have ordinary cellular precision. Rather, the spiking precision can be explained as an intrinsic cellular property while the gap junctions act to frequency- and phase-lock the network oscillations.     

Organization of galanin-like immunoreactive neuronal systems in weakly electric fish (Apteronotus leptorhynchus).

Immunohistochemical procedures were used to investigate the distribution of galanin-like immunoreactive neuronal somata, fiber pathways and apparent termination fields in the gymnotiform brain. Immunoreactive somata were observed only in the hypothalamus and were confined to preoptic, lateral and caudal hypothalamic regions. Within these areas, positive cells tended to be most concentrated in juxtaventricular nuclei. Dense immunoreactive fiber systems originating from hypothalamic regions were seen to project in separate or coalescing fiber bundles to the basal telencephalan, thalamus/tuberal diencephalon, midbrain and brainstem. The density of positive axons and boutons was quite variable, but regions which displayed the most massive network of axons included structures within the hypothalamus itself (anterior periventricular preoptic nucleus, caudal and lateral hypothalamus), ventral telencephalon (superior and ventral subdivisions), thalamic/tuberal areas (central posterior nucleus and tuberal neuropil within the ventral territory of the prepacemaker nucleus) and brainstem nuclei (dorsal reticular nucleus and the medial paralemniscal nucleus). Within these areas axons appeared more randomly distributed and varicose than along fiber tracs, and in counterstained sections were occasionally seen in apposition to unstained neuronal cell bodies and dendrites. In addition, a system of fibers was seen in the neurointermediate lobe of the pituitary. It is concluded that galanin-like immunoreactive neurons in the gymnotiform brain have a more restricted distribution than those in mammals, and that the major fiber systems emanating from the hypothalamus resemble the diverse projections of the tuberomammillary nucleus of higher vertebrates. The anatomy of galanin-like immunoreactive systems in the apteronotid brain suggests a role in neuroendocrine regulation and an involvement with anatomical areas controlling aggressive and courtship behaviour.     

Analysis of behavior-related excitatory inputs to a central pacemaker nucleus in a weakly electric fish

Gymnotid electric fish explore their environment and communicate with conspecifics by means of rhythmic electric organ discharges. The neural command for each electric organ discharge arises from activity of a medullary pacemaker nucleus composed of two neuronal types: pacemaker and relay cells. During different behaviors as in courtship, exploration and agonistic interactions, these species display specific electric organ discharge frequency and/or waveform modulations. The neural bases of these modulations have been explained in terms of segregation of inputs to pacemaker or relay cells, as well as differential activation of the glutamate receptors of these cells. One of the most conspicuous electric organ discharge frequency modulations in Gymnotus carapo results from the activation of Mauthner cells, a pair of reticulospinal neurons that are involved in the organization of sensory-evoked escape responses in teleost fish. The activation of Mauthner cells in these animals produces a prolonged increase in electric organ discharge rate, whose neural mechanisms involves the activation of both N-methyl-D-aspartate (NMDA) and metabotropic glutamatergic receptors of pacemaker cells. Here we provide evidence which indicates that pacemaker cells are the only cellular target of the synaptic inputs responsible for the Mauthner cell initiated electric organ discharge modulation at the medullary pacemaker nucleus. Additionally, although pacemaker cells express both NMDA and non-NMDA ionotropic receptors, we found that non-NMDA receptors are not involved in this synaptic action which suggests that NMDA and non-NMDA receptor subtypes are not co-localized at the subsynaptic membrane. NMDA receptor activation of pacemaker cells seems to be an efficient neural strategy to produce long-lasting enhancements of the fish sampling capability during Mauthner cell-initiated motor behaviors.     

Synaptology of the hypoglossal nucleus in the rat

Summary The purpose of this study was to define the types and distribution of synaptic terminals in the hypoglossal nucleus (XII) of the rat. Based on differences in bouton and vesicle size and shape, synaptic specializations and association with postsynaptic organelles, five types of terminals were identified in XII. In order of decreasing frequency they were: 1) S-boutons (spherical vesicles with an asymmetrical synapse); 2) F-boutons (flattened vesicles with a symmetrical synapse); 3) P-boutons (pleomorphic admixture of flattened and spherical vesicles with a symmetrical synapse); 4) C-boutons (pleomorphic vesicles with a subsynaptic cistern); and 5) Tboutons (spherical vesicles with an asymmetrical synapse and subsynaptic dense bodies). S-boutons were the predominant type found on dendrites, while boutons containing flattened vesicles were more prevalent on motoneuron somata. C-boutons were restricted exclusively to cell bodies and large dendrites, and T-boutons were seen primarily on smaller dendritic profiles. These results are, in general, comparable to those previously described in the ventral horn and cranial nerve motor nuclei in several species. However, differences were noted. Specifically, large M-boutons and axo-axonic synapses were not observed in the present study. The functional significance of these findings are discussed in relation to oro-lingual behaviour.     

The mormyrid brainstem--III. Ultrastructure and synaptic organization of the medullary "pacemaker" nucleus

The ultrastructure and synaptic organization of the presumed medullary pacemaker nucleus, nucleus c of the weakly electric mormyrid fish, Gnathonemus petersii has been investigated. Nucleus c consists of about 12-15 small (20-25 micron) neurones (P-cells), which form a group situated ventrally to the medullary relay nucleus and embedded in a neuropil of myelinated fibres and dendritic processes. The P-cells often exhibit an enhanced electron density of their cytoplasm and dendroplasm. They possess several dendrites of different diameter, a short, thin axon initial segment and a thickly myelinated axon running in dorsal direction. The pacemaker neurons are interconnected by complex electronic coupling, established by somatosomatic, dendrosomatic and dendrodendritic gap junctions. Perikarya and dendrites are frequently interconnected serially by gap junctions; dendrites showed sometimes triadic gap-junction arrangement. It is suggested that this high degree of electrotonic coupling amongst the pacemaker cells represents the first level of the highly ordered synchronization processes which characterize the electric discharge command system of Gnathonemus. Pacemaker cells receive synaptic input from club endings with mixed synapses and from bouton-like terminals with chemical synapses, both of them originating from medium-sized myelinated fibres and contacting mainly neuronal perikarya and dendritic processes. The axon initial segment receives only few synaptic inputs. Bouton-like terminals were found to be of two types according to their vesicle content, namely, boutons with ovoid, clear synaptic vesicles forming Gray type-1 synapses and boutons with pleomorphic clear synaptic vesicles forming Gray type-2 synapses. Different functional roles for the two types of boutons in modulating pacemaker cell activity are suggested.     

An atlas of the brain of the electric fish Apteronotus leptorhynchus

This atlas consists of a set of six macrophotographs illustrating the important external landmarks of the apteronotid brain, as well as 54 transverse levels through the brain stained with cresyl violet. There are 150 microns between levels and the scales have 1 mm divisions (100 microns small divisions). In general the neuroanatomy of this brain is similar to that of other teleosts except that all parts known to be concerned with electroreception are greatly hypertrophied (electrosensory lateral line lobe, nucleus praeminentialis, caudal lobe of the cerebellum, torus semicircularis dorsalis, optic tectum and nucleus electrosensorius). There are other regions of this brain which are hypertrophied or which have not been described in other teleosts, but which are not known to be directly linked to the electrosensory/electromotor system; these regions are mentioned in the accompanying text.     

Fine structure of the tuberous electroreceptor of the high-frequency electric fish,Sternarchus albifrons (gymnotiformes)

Summary Sternarchus emits low voltage biphasic pulses at about 700–900/s. These signals (and changes in them caused by external objects) are detected by the tuberous or phasic electroreceptors. We used electron microscopy to examine extracellular compartments in the current pathway to the receptor cells, which are delineated by cells joined by tight junctions. Highly specialized accessory cells were found to separate the receptor cells from the extracellular space continuous with the exterior. Except for synaptic specializations complements of intramembrane particles of cell membranes were unremarkable and did not correlate with presumed high and low resistivity. We propose an equivalent electrical circuit that is consistent with the morphological and physiological observations.     

Somatostatin-like immunoreactivity in the brain of an electric fish (Apteronotus leptorhynchus) identified with monoclonal antibodies.

The immunohistochemical localization of somatostatin-like immunoreactive (SSir) cells and fibers in the brain of the gymnotiform teleost (Apteronotus leptorhynchus) was investigated using well-characterized monoclonal antibodies directed against somatostatin-14 and -28. Large populations of SSir neurons occur in the basal forebrain, diencephalon and rhombencephalon and a dense distribution of fibers and terminal fields is found in the ventral, dorsomedial and dorsolateral telencephalon, hypothalamus, centralis posterior thalamus, subtrigeminal nucleus, the motor nucleus of vagus and in the ventrolateral medulla. Immunoreactive neurons in the forebrain are concentrated mainly in the ventral telencephalic areas, the region of the anterior commissure and entopeduncular nucleus. In a fashion similar to the large basal telencephalic cells of other species, the cells of the rostral nucleus entopeduncularis have a significant projection to the dorsal telencephalon. The preoptic region and the peri- and paraventricular hypothalamic nuclei are richly endowed with SSir cells; some of these cells contribute fibres to the pituitary stalk and gland. In the thalamus, only the n. centralis posterior stands out for the density of SSir cells and terminals; these cells appear to project to the prepacemaker nucleus, thus suggesting an SS influence on electrocommunication. In the mesencephalon most SSir cells occur in the optic tectum, torus semicircularis and interpeduncular nucleus. The rhombencephalic SSir cells have a wider distribution (central gray, raphe, sensory nuclei, reticular formation, electrosensory lateral line lobe and surrounding the central canal). The results of this study show the presence of SS in various sensory systems, electromotor system and specific hypothalamic nuclei, suggesting a modulatory role in the processing of sensory information, electrocommunication, endocrine and motor activities.     

The larval electric organ of the weakly electric fish Pollimyrus (Marcusenius) isidori (Mormyridae, Teleostei)

Summary The larval electric organ ofPollimyrus isidori consists of four longitudinal tubes, a dorsal and a ventral pair, which begin behind the skull, end at the beginning of the caudal peduncle and show myotomic segmentation. The elementary units are, apparently, transformed muscle fibres called electrocytes. They are shorter and thicker than muscle fibres, with long stalks and are found in the medial part of the deep lateral muscle. Electron microscopy reveals a clear difference between the anterior and posterior face of the electrocyte. Anteriorly, deep linear invaginations of the surface membrane together with many small vesicles of about 100 nm diameter can be seen. Posteriorly, many plasma membrane invaginations and vacuoles are found together with numerous cytoplasmic organelles — pleiomorphic nuclei, Golgi apparatus, oblong mitochondria and multivesicular bodies. The stalk originates at the posterior face and the nerve terminals are situated at the distal end of the stalk. In the electrocyte, myofibrils, similar to those found in muscle fibres, can be detected with clearly visible Z lines but with only a suggestion of H zones. Two bundles of myofibrils can be seen arranged orthogonally in the electrocyte. Strong acetylcholinesterase activity was found on the anterior face and on the innervated stalk. Under the given recording conditions the overall discharge amplitude of the larval electric organ reaches a maximum of about 100 mV peak to peak. The pulse duration is 1 millisecond and the main phase is head-positive.     

The distribution of excitatory amino acid binding sites in the brain of an electric fish, Apteronotus leptorhynchus.

The distribution of three types of exitatory amino acid receptors was examined in the brain of a high frequency weakly electric fish, Apteronotus leptorhynchus, by localizing the binding sites of ligands selective for mammalian kainic acid (KA), quisqualate (AMPA) and N-methyl-D-aspartate (NMDA) receptors. All three binding sites were densest within the forebrain and in certain hypothalamic nuclei (nucleus tuberis anterior, inferior lobe). The core of the dorsal forebrain (dorsal centralis) had a very high density of NMDA binding sites and only moderate levels of AMPA and KA binding sites, while this was reversed for the dorsolateral forebrain. The AMPA and NMDA binding sites were found throughout the brain while KA binding sites were relatively restricted and were absent from most of the brainstem. The cerebellar molecular layer contained a very high density of KA and AMPA binding sites but almost no NMDA binding sites; the granular layer had a low density of AMPA and NMDA binding sites but was lacking in KA binding sites. All three types of binding sites were found within the electromotor system (nucleus electrosensorius and prepacemaker nucleus) at sites where the iontophoresis of glutamate causes species-specific behaviours. KA binding sites were found at only two sites along the electrosensory afferent pathways: (1) in the molecular layer of the electrosensory lateral line lobe, associated with a feedback pathway emanating from granule cells of the overlying cerebellum, and (2) in the lateral nucleus praeminentialis dorsalis, associated with a descending pathway emanating from the torus semicircularis. NMDA and AMPA binding sites are found throughout the electrosensory pathways. Within the electrosensory lateral line lobe the NMDA binding sites were predominantly associated with the feedback pathways terminating in its molecular layer and not with the deep neuropil layer containing primary electroreceptor afferents.     

Electroreceptive single units in the mesencephalic magnocellular nucleus of the weakly electric fish gymnotus carapo

Summary 1. Extra- and intracellular recordings from single units in the magnocellular mesencephalic nucleus (MMN) of the torus semicircularis, related to the fast electrosensory system are reported for the weakly electric fish Gymnotus carapo (Gymnotidae). 2. The non-spontaneously active units responded with single action potentials to the electric organ discharge (EOD) and to artificial electrical pulses with a very short latency of 0.8–1.5 ms. This strongly suggests, in agreement with morphological data, that transmission takes place through electrical synapses. 3. The dynamic range (probability and latency of the single action potential) of the response is extremely narrow and about the same as found in the relevant electrosensory fibres. Intracellular stimulation gives the same response characteristics and dynamic range. 4. The recovery of the response was studied in detail using different stimulus combinations of double pulses at varying delays. Under all conditions, the recovery period to evoke a test response after a conditioning stimulus and response increased in length with the strength of the conditioning stimulus. Inversely, the conditioning stimulus to prevent the unit from firing again had to be stronger as the delay between the two stimuli was increased. 5. Since there is no evidence of neural inhibition causing the long lasting and graded recovery characteristics for MMN units, an attempt was made to explain the findings by classical neurophysiological considerations adapted for electrical synaptic transmission (current sink theory). 6. This neural mechanism means that, if at all, the relatively weaker stimulus is not responded to, which protects the fish from being jammed by external pulses of physiological amplitude. In contrast, very strong foreign pulses can completely abolish responses to own EODs especially when timed appropriately. Both effects are discussed in view of their significance for the fish's electrosensory system and communication.     

Retinal afferents to the thalamic mediodorsal nucleus in the rock cavy (Kerodon rupestris)

The MD has reciprocal connections with the ventromedial prefrontal cortex (PFC) and with limbic cortices and appears to participate in learning and memory-related processes. In this study, we report the identification of a hitherto not reported direct retinal projection to the MD of the rock cavy, a typical rodent species of the Northeast region of Brazil. After unilateral intravitreal injections of cholera toxin subunit B (CTb), anterogradely transported CTb-imunoreactive fibers and presumptive terminals were seen in the MD. A few labeled retinal fibers/terminals detected in the MD of the rock cavy brain show clear varicosities, suggesting terminal fields. The present work is the first to show a direct retinal projection to the MD of rodents and may contribute for elucidating the anatomical substrate of the functional involvement of this thalamic nucleus in the modulation of the visual recognition, emotional learning and object-reward association memory.     

Neurohistological analysis of the lateral lobe in a weakly electric fish,Gymnotus carapo (Gymnotidae,Pisces)

Summary The cyto- and fiber architecture of the lateral lobe (LL) of Gymnotus carapo was investigated using Nissl, Golgi and reduced silver stains as well as 1 semi-thin sections. The neurons and fiber tracts are distributed in six layers. The first layer is subdivided into two sublayers: 1A where the primary afferent fibers run in rostro-caudal direction and 1B where these fibers terminate and the large multipolar neurons can be found. The 2nd layer consists of a single row of adendritic, pear-shaped neurons. The axons of these neurons enter the 4th layer and leave the lateral lobe in medial direction. The 3rd layer contains the granular cells of two different types: granular cells with two dendritic trunks directed into dorsal and ventral directions respectively, and granular cells in which, instead of the dendritic trunk, the axon emerges from the dorsal pole of the perikaryon. The axon can be followed up to the 6th layer. The 4th layer consists of bundles of nerve fibers. Beside the axons of the pear-shaped neurons the bundles contain also the axons of the pyramidal neurons (5th layer) leaving the lateral lobe. The 5th layer contains the perikarya of the pyramidal neurons. They have two separate dendritic arborizations, one directed ventrally and entering layer 1B and another directed dorsally and penetrating into the 6th layer. Their axons join the 4th layer and run in medial, rostro-medial or rostral direction depending upon the localization of the neurons in the lateral lobe. The 6th layer (crista cerebellaris) consists of three sublayers. Sublayer 6A contains fine myelinated fibers of unknown origin; sublayer 6B contains fine, mainly non-myelinated fibers originating from the mesencephalon, sublayer 6C is built up of non-myelinated fibers originating from the cerebellum. — A preliminary diagram of the neuron circuits and of the synaptic arrangements involved in the relay of lateral-line organ impulses is suggested.Supported by Research Grant No. 659440 accorded to Dr. T. Szabo by the Direction de Recherches et Moyens d'Essais (D. R. M. E.).Visiting investigator, aided by Institut national de la Santé et de la Recherche Médical (I. N. S. E. R. M.).Address: Groupe des Laboratoires du C. N. R. S. 91190 Gif-sur-Yvette, France.     

Morphological correlates of electrotonic coupling in the magnocellular mesencephalic nucleus of the weakly electric fish Gymnotus carapo.

The magnocellular mesencephalic nucleus (MMN) of Gymnotus carapo was studied by electron microscopy. This particular nucleus, characteristic of weakly electric fish, contains two principal classes of neuron. (1) Large neurons (25-35 mum): these are rounded unipolar cells, with the perikaryon partially covered by a sheath of compact myelin. The axon leaves the neuron as a short thick unmyelinated process not resembling the initial segment of multipolar neurons. The axon branches profusely and becomes myelinated very close to its origin. The perikaryal surface not covered by the myelin sheath receives abundant club endings. The synaptic interface between club endings and large neurons is characterized by alternating gap junctions and attachment plaques. In addition, at the periphery of the club endings, "active" zones are generally present, and this synapse is therefore a "mixed" synapse. (2) Small neurons (5-12 mum): these are uni- or bipolar cells, scattered throughout the nucleus, and occasionally, grouped in small clusters. Gap junctions were not observed between neuronal perikarya in such clusters. The synaptic investment of small neurons is formed by long cup endings which almost completely encircle the perikarya. The synaptic interface between cup endings and the perikarya of small neurons is characterized by large areas of gap junctions. A single cup ending establishing gap junctions with two small neurons within the plane of the section was frequently observed and this arrangement provides a morphological basis for electrotonic coupling between small neurons by way of presynaptic fibres. In the neuropil of the MMN, there are abundant synaptic islands constituted by a large axon terminal in synaptic contact with small unidentified profiles; both synaptic elements are surrounded by numerous thin glial lamellae. At the synaptic interface, in the islands, both gap junctions and "active" zones are present. The synaptic islands must also be considered as "mixed" synapses. The morphological results presented here correlate with electrophysiological data (Szabo et al., 1975). The very short delay (0.8-1.3 ms) of the MMS response to the fish's own electric organ discharge can only be explained by the existence of electrotonic transmission along the neuronal chain of the electrosensory pathway. The presence of gap junctions between club endings and large neurons provides a morphological basis for electrotonic transmission at the mesencephalic level of the electrosensory pathway.     

Synaptology of the olfactory bulb of an elasmobranch fish, Sphyrna tiburo

The ultrastructure of the elasmobranch olfactory bulb was examined in order to determine the synaptology of the olfactory circuitry in the bonnethead shark, Sphyrna tiburo. The compartmentalization of the bulb, together with the lack of mitral cell basal dendrites, suggests a different way of performing lateral communication between mitral cells of the olfactory bulb. The results show that granule cells assume an important role by directly interlinking mitral cells. A corollary of this is the segregation of the input onto the mitral cell dendritic arborization: afferent fibers synapse onto the intraglomerular mitral terminals, whereas most local circuit interactions utilize extraglomerular synapses located on the shafts and the somas of the mitral dendrites. Therefore, the elasmobranch synaptic pattern is different from that of higher vertebrates; This might represent the use of a different neural route to achieve the same processing task.     

Receptor position, not nerve branch, determines electroreceptor somatotopy in the gymnotiform fish (Apteronotus leptorhynchus)

The supraorbital (SO) nerve branch of some weakly electric teleosts innervates electroreceptors on the entire rostral snout and therefore excludes the infraorbital (IO) branch. A ventral twig of SO innervates the ventral snout (normally IO territory) and projects into the electroreceptive lateral line lobe in an IO pattern. This suggests that afferents to adjacent snout receptors can take widely divergent pathways (different nerve branches) to the electrosensory lateral line lobe (ELL) yet retain somatotopy centrally. We conclude: (1) that there is intrabranch somatotopy within these nerves, and (2) that receptor position, not nerve branch, determines ELL somatotopy.