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The anatomical connection of the magnocellular isthmic nucleus with the optic tectum was investigated with the axonal tracer biotinylated dextran amine. Following iontophoretic injection of this tracer into different areas of the chick optic tectum, neurones of both magno- and parvocellular isthmic nuclei were labelled together in a topographical arrangement. The number of labelled neurones in the parvocellular nucleus was generally higher than in magnocellular. Using different locations of the tracer injections, systematic shifts in the location of the labelled neurones were detected. The labelled axons were seen to course along the shortest possible distance between the injection site and the cells of origin, i.e., the ventral part of the tectum received projections from neurones located ventrally in the isthmic nuclei, the dorsal tectum from neurones in the dorsal part, and the lateral extension of the tectum from neurones lying midway along the nuclei. This parallel and topographic projection of the two nuclei was primarily observed in sagittal sections. After tracer injections into the magnocellular nucleus, the terminal arbours were seen to extend from the deep layers (11-12) to layer 2 of the tectum. The projections observed appeared to be topographically organised, and furthermore appeared to be parallel with and complimentary to previously described projections of the parvocellular isthmic nucleus.

The optic tectum is reciprocally connected to the nuclei isthmi pars magnocellularis (Imc) and pars parvocellularis (Ipc), which have different modulatory effects on optic transmission. We studied the axon arbourisation of these isthmic nuclei in the optic tectum in order to differentiate between them using Golgi-impregnated preparations both in chickens and pigeons. In addition, sections from animals injected with the anterograde tracer biotinylated dextran-amine (BDA) into the Imc were examined in the bright-field and electron microscope to identify the axon arbourisations and terminals. Also, GABA immunogold stained sections were examined in the electron microscope. In Golgi preparations, slab-like (or poplar tree-like) axon terminal arbourisations of both magnocellular and parvocellular isthmic nuclei neurons were found extending to the tectal surface, with similar branching patterns, but different lengths. The axon arbourisations extending from layer 5 of the optic tectum to the surface were termed type 1, whereas those extending from the internal (12-11) layers to the tectal surface were termed type 2. Type 2 arbourisations very closely matched arbourisations observed in BDA injected material, indicating that Imc neurons gave rise to type 2 arbourisations. The two kinds of axon arbourisation in the external tectal layers were alike in both types of bird, except for the width, which was about 10 mum larger in the type 2 axon arbour. Controlling for size, there was no significant difference between chicks and pigeons. The significance of these afferents in the optic tectum is discussed.

The nucleus lentiformis mesencephali magnocellularis (nLMmc) is an essential part of the accessory optic nuclei and is responsible for stabilization of the horizontal eye movement. The morphology of this nucleus and its intrinsic structural connectivity were studied with Golgi, biotinylated dextran amine anterograde immunotracer and GABA immunostaining methods by light and electron microscopy. In the Golgi preparations neurons of large, medium-large, medium and small sizes were distinguished. The small neurons are GABA-immunopositive local circuit neurons, the others are proposed to be partly projection, partly local circuit neurons. The large and medium-large projection neurons are located in a tight topographical relationship observed in the Golgi preparations. The dendrites of the large and medium-large cells are also observed to be in close proximity with each other, and also with retinal fibre terminals. The morphological arrangement suggests that the retinal fibres make synaptic contacts with dendrites from both types of cell, and this is confirmed by the examination of retinal fibre terminals using electron microscopy. The optic fibre terminals establish synaptic contacts with small dendritic branches, dendritic processes and dendritic spines of large and medium-large neurons in the nLMmc. This arrangement allows the two types of nLMmc neuron access to very similar, if not identical, inputs, which may facilitate some of the different aspects of visual processing. Optic transmission by these cells may be modulated by the GABA-immunopositive terminals from various local circuit neurons, and very probably from GABAergic myelinated fibres as well, which may originate from the contralateral nLMmc and/or the visual Wulst., (Copyright 2003 S. Karger AG, Basel)

The intrinsic neuronal organisation in the nucleus of the basal optic root of chickens was investigated. The divergent connections with various areas and the functional complexity of the nucleus require a complex intrinsic structural arrangement. Therefore, an analysis of Golgi impregnated material, ultrastructure, GABA-immunocytochemistry and biotinylated dextran-amine anterograde tracer analysis of the nucleus was carried out. In the Golgi analysis, a characteristic dendritic ramification pattern of two types of putative projection neurons was observed. These neurons form dendritic nests with their overlapping dendritic terminal sections, that develop synaptic fields with the optic fibre terminals. These synaptic fields were confirmed by electron microscopy. GABA-immunopositive terminals synapse with distinct loci of the dendritic trees of projection neurons; they may therefore play an important role in the inhibitory-modulatory system of the nucleus of the basal optic root. The GABA-immunopositive terminals derive from small and/or elongated local circuit neurons which receive retinal afferents, and from myelinated fibres afferents to the nucleus of unknown origin.

Three types of local circuit neurons have recently been reported in the homing pigeon hippocampus. The principal type appears to be constituted by the medium-sized angular or ovoid local circuit neurons that occur in all layers of the hippocampus. The current Golgi study has revealed that these neurons can be classified according to their axonal arborisation extension: (1) in all directions, (2) principally medio-laterally, or (3) dorso-ventrally. The local circuit neurons with dorso-ventral axon arborisation are present only in the subpyramidal layer. Serial sections of a Golgi-impregnated medium-sized, multiangular local circuit neuron in the pyramidal layer and a small, ovoid neuron in the suprapyramidal layer were investigated in the electron microscope. Some of these sections were processed for GABA immunogold cytochemistry. The soma and large dendrites of both neurons displayed GABA immunogold labelling. On the soma of medium-sized local circuit neuron there were numerous terminals; on the soma of the small one relatively fewer terminals were observed. The terminals contained round and/or flat synaptic vesicles. The long axonal branches of the neurons exhibited varicosities containing flattened or pleomorphic vesicles. Axo-dendritic, axo-somatic and a few axo-axonic synapses were observed. The large dense axon arborisation field of medium-sized local circuit neurons is properly situated to modulate intrinsic hippocampal activity and that of the small local circuit neurons is well situated to modulate the hippocampal input in the suprapyramidal layer.

In the present study the telencephalic connections between the centres of the tectofugal and thalamofugal pathways were investigated with Phaseolus vulgaris leucoagglutinin and biotinylated dextran-amine anterograde tracers in chicken using light and electron microscopy. No direct connection was found between the visual Wulst and the ectostriatum or the telencephalic centres of the tectofugal and thalamofugal pathways. Besides other projections, the visual Wulst emitted fibres also to the middle and lateral parts of the hyperstriatum ventrale. Further experiments revealed that the middle part of the hyperstriatum ventrale projected to the ectostriatum centrale and periphericum and established an indirect connection between the visual Wulst and the ectostriatum. The lateral part of the hyperstriatum ventrale sent a few efferent fibres toward the diencephalon and brainstem, but projected massively to the ectostriatum periphericum, neostriatum intermedium pars laterale, the ventral part of the neostriatum caudale and the archistriatum dorsale. Considering that these areas are structures of the tectofugal circuitry as well, the presence of these connections may result in a more elaborate visual processing. The neostriatum may be an associative visual center and possibly a modulatory area toward the archistriatum intermedium dorsale, by which visual information may mediate, modulate and control the movements.

In Golgi preparations of the chicken diencephalon, various types of cells and fibres were studied in the nucleus dorsolateralis anterior thalami (DLA). Two groups of neurons were found: projection neurons with long axons and interneurons with locally branching axons. The projection neurons varied in the different areas of the DLA. In the medial part the neurons are large cells with long, moderately spiny dendrites, and in the dorsal part there are small cells with short, wavy and moderately spiny dendrites. These neurons differ completely from those found in the rostral and lateral parts, where the neurons have medium-sized cell bodies and curving, spiny dendrites, which branch tuft-like or with bifurcations. In the rostral and lateral parts of the DLA, thick afferent fibres were impregnated which developed their terminal branchings among the neurons. Owing to their terminal branching pattern and the shape of the terminals they are thought to be optic fibres. The terminal pattern of these fibres is similar to the optic terminals in the LGB of the mammalian brain. The interneurons are GABA positive, as attested by immunostaining in light microscopic and EM specimens. There are rather few of them. The HRP-filled projection neurons and the surrounding neuropil were investigated under EM: synaptic connections around the large terminals and/or around dendrites were identified, but this synaptic arrangement does not display the characteristics of a synaptic glomerulus.

Following a demonstration of Golgi-impregnated neurons and their terminal axon arborization in the optic tectum, the neurons of the nucleus parvocellularis and magnocellularis isthmi were studied by means of postembedded electron-microscopical (EM) gamma-aminobutyric acid (GABA)-immunogold staining. In the parvocellular nucleus, none of the neuronal cell bodies or dendrites displayed GABA-like immunoreactivity in EM preparations stained by postembedded GABA-immunogold. However, numerous GABA-like immunoreactive and also unlabeled terminals established synapses with GABA-negative neurons. GABA-like immunoreactive terminals were usually found at the dendritic origin. Around the dendritic profiles, isolated synapses of both GABA-like immunoreactive and immunonegative terminals established glomerulus-like structures enclosed by glial processes. All giant and large neurons of the magnocellular nucleus of the isthmi displayed GABA-like immunoreactivity. Their cell surface was completely covered by GABA-like immunoreactive and unlabeled terminals that established synapses with the neurons. These neurons are thought to send axon collaterals to the parvocellular nucleus; their axons enter the tectum opticum. The morphological characteristics of neurons of both isthmic nuclei are like those of interneurons, because of their numerous axosomatic synapses with both asymmetrical and symmetrical features. These neurons are not located among their target neurons and exert their modulatory effect on optic transmission in the optic tectum at a distance.

The neuronal structures and their possible connections in the optic tectum of chicks were studied by using Golgi impregnation, in light microscopy, and Golgi-GABA immunogold staining in electron microscopy. The terminals of the optic fibers displayed different patterns and orientation in various laminae of the avian optic tectum. The shape of the branching and the terminals of the optic fibers conformed to the postsynaptic neuronal structures. In Golgi preparations, the terminals in tectal layers 4 and 5 seemed to be located rather densely, and they contact, among other things, the 'dendritic terminal sections' of large ganglion cells of layer 13 of the tectum. This connection could be responsible for direct optic transmission via ganglion cells to the nucleus rotundus. Additionally, the contacts established by optic terminals in these layers with the tectal neurons arranged with their dendrites parallel to the surface of the tectum, could provide the structural basis for an inhibitory system. The terminals of isthmic nuclei were found in this optic lamina, too. The optic terminals in layer 7 contacted the dendritic side branches of some radial tectal neurons.

After PhA-L injection into the tectum opticum of chickens, column-like labelled terminal arborizations were found in tectum and also labelled neurons of Ipc and Imc in the corresponding sections. The PhA-L labele proved the projection from both Imc and Ipc neurons to tectum; their terminal axonarborizations were clearly discernible. Column-like terminal arborizations of different sizes were found both in PHA-L and Golgi impregnated preparations. GABA immunostaining displayed GABA positive neurons in Imc. The EM-Golgi study corroborated that the axon-terminals of Imc neurons established symmetrical synapses in the tectum. The results of the present study support the existence of an inhibitory feedback loop from Imc neurons to the tectum.

Investigation of the chick archistriatum revealed that it was not possible to distinguish distinct sub-regions on the basis of their Golgi architecture, despite the fact that the pigeon archistriatum has been suggested to comprise "amygdaloid" and "sensorimotor" divisions. Nine sub-types of projection neuron and four of local circuit neuron were identified in the chick archistriatum. Projection neurons were generally larger with thicker dendrites than those in other regions of the chick telencephalon. A greater proportion of these projection neurons also had highly densely spiny dendrites. These findings suggest that archistriatal neurons receive a large, possibly complex afferentation and project considerable distances. Large and medium-sized local circuit neurons with varicose axon branches and relatively large neurogliaform cells were characteristic of the archistriatum. All types of archistriatal neuron were identified in both 28 and one day old chicks. However, presumptive highly densely spiny projection neurons appeared relatively immature in the one day old chick archistriatum.

After having iontophoretically injected Phaseolus vulgaris Lectin into nucleus rotundus, labelled terminals were examined in ectostriatum centrale by EM. These terminals contained round synaptic vesicles. They were observed earlier by Golgi method and proved to be of rotundal origin by Phaseolus Lectin tracing method. The labelled terminals establish synapses, on large and small dendritic truncs of projection and local circuit neurons, and also contact spines and dendritic processes of projection neurons. They were observed on soma of GABA immunopositive local circuit neurons, and also on dendrites. Some observations completed the already known data on fine structure of the chicken ectostriatum centrale.

The structural arrangement of nucleus rotundus was studied by Golgi method. Large, multiangular principal neurons, their dendrites and dendritic terminals were observed. The long dendrites and their side-branches course parallel and/or perpendicular to each-other and they are arranged about in dorso-ventral latero-medial and rostro-caudal directions. The dendrites and their side-branches develop characteristic terminal branchings. These dendritic terminals overlap each-other and the area is called dendritic terminal field. The tecto-rotundal fibers traverse the nucleus in large bundles and the final sections of fibers join to the dendrites of principal neuron and terminate in dendritic terminal fields.

In Golgi impregnated ectostriatum centrale of telencephalon of one-day-old chicken two types of neuron: projection neuron and interneuron with large axonal field and varicose axonal preterminals and terminals, were identified and examined in EM preparates. In the serial EM sections the morphological features of the two neurons types were observed. The projection neuron is characterized by the few axo-somatic synapses on the cell membrane, which are of symmetrical type. The INs, however, have numerous axo-somatic synapses on cell membrane both of symmetrical and asymmetrical types. Also the axonterminals were analysed.

The study demonstrates one kind of the afferent fibers in ectostriatum in Golgi preparates. These fibers enter the ventro-medial border of the area. The primary section and further course and branches, as well as the terminal arborization of these fibers were observed. Also the maturation process of the branchings of the fibers was studied in the Golgi preparates after hatching. The fiber-networks found in one-day-old and 28-day-old chicken ectostriatum centrale were compared.

The brains of kittens prenatally exposed to ethanol were studied by the rapid-Golgi method at PN1 and PN9 days. The sizes of the alcohol damaged brains were different. Delayed gyrification was observed on the brain surface. The neurons in subcortical (thalamic) centres and cortical areas developed later than in normal animals. Between days PN1 and PN9 rapid changes occurred in the development of the structural elements of brains of prenatally alcohol exposed kittens.

The existence of Golgi type II neurons was verified in the anterior intralaminar central lateral (CL) nucleus of the cat thalamus, and its projection cell types were identified, by means of Golgi impregnation. CL principal neurons were found to display a large- or medium-sized cell body and a radiate dendritic pattern. Their primary dendrites were limited in number, and had a rather long course; they were poorly ramified. The axons of principal neurons were impregnated only occasionally and for a short distance. Projection neurons of the 'bushy' or tufted type, described in the main thalamic sensory nuclei, were not identified in the CL in the present study. Typical Golgi type II neurons were found throughout CL. They were mainly small-sized, and displayed a rich dendritic arborization characterized by dendritic appendages. The axons of Golgi type II neurons were seen to give rise to extensive local arborizations. The present findings indicate that in the cat CL, principal cells are mainly represented by radiate neurons. Typical local circuit neurons also are evident in CL, suggesting that the activity of anterior intralaminar structures is regulated by intrinsic mechanisms similar to those operating in the main thalamic relay nuclei.

In the Golgi preparation of visual Wulst of chicken four types of projection neurons were found: type 1a, 1b, 1c, and 1d neurons, which are distinguished on the basis of their dendritic ramification pattern and especially on the density of the dendritic spines. Type 1a has large dendritic tree with moderately dense spiny dendrites. Type 1b has very dense spiny dendrites. Type 1c is a small neuron with moderately dense spiny dendrites. Type 1d is a star-pyramid-like neuron with a short, bifurcating apical dendrite. The final dendritic pattern and spine density of projection neurons was found to develop at the end of the first month. In the Wulst short axon cells (interneurons-INs) of different types occur: large, medium-sized and small INs can be observed. Their axon-arborizations are significantly different from each other. Some of them are GABA-immuno-positive neurons, which are very probably inhibitory interneurons. Stellate-like neurons also occur in IHA and HIS. These neurons have sparsely spiny dendrites and locally arborizing axons.

Our investigations try to reveal the morphological changes found postnatally at different levels and centres of central nervous system of kittens of cats chronically treated with ethanol during their pregnancy and lactation. The changes found in neurons of lateral geniculate nucleus (LGN) were analyzed in Golgi-stained preparations from brains removed on the first or on the ninth postnatal days. The data were computerized. The changes measured in neurons refer to their maturation process: a significant delay of differentiation of the neurons occurs in LGN. Also a delayed gyrification of brains was observed.

The Golgi method more than hundred years old can reveal new results also in the current research of CNS. The study provides examples for using the Golgi method and demonstrates the types of neurons, the various types of interneurons, characterizes the stellate cells in layer IV of the cortex. The Golgi method is applicable for the observation of maturation process and also for demonstrating different pathological alterations of neurons in the CNS.

This study has been carried out by light microscopy on 3 Golgi-Kopsch impregnated brains of young adult rabbits. It is shown that chandelier cells exist within the rabbits' cerebral cortex. In the rabbit, the chandelier cell is a medium ranged bipolar interneuron in layer II/III with a characteristic axon which forms a plexus with a diameter of about 350-500 micrometers in the horizontal and 200-350 micrometers in the vertical direction; the end of each ramulus forms the typical "candlestick", a little vertical string of 1-6 boutons on an axon fibre. These boutons form contacts with all parts of pyramidal cells in layer II and the upper part of layer III. Similarities and differences with respect to previous descriptions of these cells in other species are discussed.

A study of was carried out of Golgi impregnated material in two regions of the paleostriatal complex of the chick telencephalon, the lobus parolfactorius and paleostriatum augmentatum. As in our previous investigation of the chick medial hyperstriatum ventrale, two major classes of neurons were observed in the paleostriatum: a Golgi I type neuron (type 1) with long axon (putative projection neuron) and a Golgi II type neuron (type 2) with short axon (putative local circuit neuron). Based upon the nature of the axon (bifurcating or nonbifurcating, ascending or descending) and of the dendrites (spiny or aspinous, and thickness), the following subclasses (types) were identified: two projection and three local circuit neurons in the lobus parolfactorius and two projection and two local circuit neurons in the paleostriatum augmentatum. In addition to known differences in developmental chronology and extrinsic connectivity, the lobus parolfactorius clearly differs from palaeostriatum augmentatum in cellular composition and organization. From its cytoarchitectonic appearance we would suggest that the lobus parolfactorius is the paleostriatal region of greater complexity.

The Golgi architecture of the nucleus caudatus in rabbit, cat, monkey and human material was analysed. The brains were prepared by Golgi--Kopsch impregnation. The fairly divergent types of neurons practically belong to two main groups: projective or efferent neurons and local- or interneurons. The efferent neurons -- as it has been confirmed by experimental studies -- establish far contacts with various regions of the brain. According to the Golgi picture, their axon emits several collaterals, which produce local connections. The interneurons have only locally arborizing axon. The are mainly responsible for intrinsic connections of the nucleus. In both main groups of caudate neurons, several types and subtypes were observed. The number of the types and subtypes of the neurons show an increasing tendency in the phylogenetic series.

The rhesus monkey's visual cortex was studied on Golgi material. The terminal arborization of the geniculate fibres and non-specific vertical fibres have been analysed. The interneurons (intrinsic neurons) of the area described in detail and classified on the basis of their axonal and dendrite arborizations. The stellate neurons in layer IV are discussed.

Two major classes of neurons were observed in Golgi impregnated material of two regions of the hyperstriatum ventrale (HV) (medial and rostral HV) of the chick telencephalon: a Golgi I type neuron with long axon (putative projection neuron) and a Golgi II type neuron with short axon (putative local circuit neuron). On the basis of the nature of the axon (bifurcating or non-bifurcating, ascending or descending) and of the dendrites (spiny or aspinous, and thickness), the following subclasses (types) were identified: two long axon (projection) and three short axon (local circuit) neurons in the medial (mid-telencephalic) hyperstriatum ventrale, and one major long axon (projection) and two short axon (local circuit) neurons in the rostral hyperstriatum ventrale. Possible patterns of intraregional connections between these neurons are suggested on the basis of cytoarchitectonics. The differences in cellular types and in internal connectivity patterns strongly suggest, in agreement with physiological and behavioural observations, that the medial (mid-telencephalic) hyperstriatum ventrale distinctly differs in cellular morphology from other parts of hyperstriatum ventrale in so far as it displays a greater diversity of neuronal types with an apparent higher degree of complexity.

Neurons displaying a thalamo-cortical projection were marked by means of the retrograde transport of horseradish peroxidase (HRP), and the labeled elements were compared with neurons impregnated by the Golgi technique. Injections of HRP into the posterior area of the limbic cortex resulted in its uptake by various anterior thalamic nuclei, especially the anteroventral nucleus. HRP-positive cells are characterized by their position, dendritic orientation, and the shape and size of their somata. On the basis of the combined HRP-and Golgi-analysis three different types of thalamo-cortical relay neurons can be distinguished.

The morphology of geniculo-cortical relay neurons (GCR-neurons) of tree shrew, rat and cat differs intraspecifically and interspecifically from each other. Intraspecific differences in the cat have been explained functionally by the W-, X-, and Y-characteristics of cells (Wilson et al. 1976). Analogous morpho-functional correlations may also explain the morphological differences in tree shrew and rat. The interspecific differences in the morphology of GCR-neurons seem to be closely correlated to the levels of visual specialization in the three species in which the rat represents a basal developmental stage.

The neuronal structure of the amygdaloid complex was studied in cat with Golgi-Kopsch perfusion technique. Four types of neurons were distinguished: the projective neurons (longaxonal), with the structure being different in the area anterior, corticomedial and basolateral parts of amygdala; the Golgi IIa neurons (shortaxonal), observed in all nuclei of the amygdala; the Golgi IIb neurons (mediumaxonal), mostly observed in the dorsal part of the lateral nucleus; the Golgi IIc, neuroglioform type of neurons with short but very profusely arborized axons, present exclusively in the ventrolateral area of the basolateral part of amygdala. In addition, some afferent fibers have been visualized in the basolateral part of amygdaloid complex.

Different types of neurons in the ventral geniculate nucleus of the thalamus of chicks were visualised by Golgi impregnation. The dendritic tree of projection neurons branched in a sphere-like territory in both the ventral and middle areas of the lamina externa. The dendrites of projection neurons in the lamina interna descended into the lamina externa and entered both the ventral and middle dendritic areas. One or two dendrites of the lamina interna neurons also emitted branches that developed a dorsal sphere-like dendritic territory. Optic terminals labelled by Golgi impregnation or injection of biotinylated dextran amine were found in these dendritic territories gathered into groups. They established synapses in these areas (synaptic islands or fields without a glial sheath) with different dendritic profiles, and a few gamma-aminobutyric acid (GABA)-positive terminals synapsed with them. No glomerulus-like synaptic complexes ensheathed by glial processes were found. Optic terminals also contacted the stem dendrites of projection neurons and GABA-positive neuron cell bodies and dendrites. Numerous synapses established by both optic and GABA-positive terminals were found on the proximal dendritic stems of the lamina interna projection neurons. Copyright © 2004 S. Karger AG, Basel [ABSTRACT FROM AUTHOR]

The ramification patterns and terminals of optic fibres in layers 2 and 3 of the optic tectum were studied in Golgi-stained and immunolabelled preparations made from the brains of chicks and pigeons. The different neuronal structures of layers 2 and 3 were also examined. In Golgi preparations, two types of optic fibre were found both in chick and pigeon tectum according to their thickness and terminal branching patterns. The same types of optic fibres were also found to be present in the anterograde tracer experiments after iontophoresis of biotinylated dextran amine into the optic nerve. The varicose terminals of thin fibres mostly terminated on terminal dendritic sections of radiate and pyramidal-like neurons, contacting them on their apical dendrites. The medium-thick fibre terminals in layer 2 mainly established synapses with horizontally extending dendrites, which may therefore be contacts with inhibitory local circuit neurons. The medium-thick optic fibre bushy-like arborisation in layer 3 established synapses with larger dendrites and also stem dendrites. Their terminals formed groups with different dendritic profiles, some of which were partly covered by glial processes, and/or were located among converging dendrites. The presence of these glomerular-like synapses in layer 3 proves that the optic terminals in layer 3 also take part in the transmission of optic impulses to the nucleus rotundus. Copyright © 2003 S. Karger AG, Basel [ABSTRACT FROM AUTHOR]

Neurons and fibres in the chick and homing pigeon hippocampus were described following Golgi impregnation. Two principal classes of neurons were distinguished: projection neurons with distant projecting axons and spiny dendrites, and local circuit neurons. In the homing pigeon and chicken hippocampus there are three types of projection neurons: pyramidal, pyramidal-like and multipolar. The pyramidal and pyramidal-like neurons are only found in the central ’pyramidal’ layer of the hippocampus whereas multipolar neurons are present in the suprapyramidal, pyramidal and infrapyramidal layers. The axon of projection neurons typically emits several varicose collaterals from the initial section. Most of these collaterals extend along the infrapyramidal layer of the hippocampus, while others ascend to the pyramidal and suprapyramidal layers where they branch. The number of impregnated axon collaterals was higher in the homing pigeon than in the chick hippocampus. A variety of multiangular/ovoid local circuit neurons ranging from small to large size are found in the homing pigeon and chick hippocampus. Their axons develop local arborisation of varicose branches, the extent of which varies with the type of local circuit neurons. The density of GABA immunopositive local circuit neurons was found to be greater in the homing pigeon than in the chick. The profuse arborisation of projection neuron axon collaterals and the higher density of GABA-immunopositive local circuit neurons in the homing pigeon hippocampus may underlie the differences in hippocampal function between the homing pigeon and chick, and this complex local connectivity may contribute to the ability of spatial orientation and memory. [ABSTRACT FROM AUTHOR]