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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of computational neuroscience 7 (1999), S. 71-87 
    ISSN: 1573-6873
    Keywords: turtle ; dendrite ; integration ; timing ; microcircuit
    Source: Springer Online Journal Archives 1860-2000
    Topics: Computer Science , Medicine , Physics
    Notes: Abstract A temporal dispersion window is the time required for a volley of action potentials on presynaptic axons to cross the dendritic arbor of a postsynaptic neuron. The volley produces a series of unitary postsynaptic potentials (PSPs) on the postsynaptic neuron. Temporal dispersion is, thus, one factor that can influence the integration of unitary PSPs and the production of action potentials in cortical neurons. Temporal dispersion windows for neurons in the visual cortex of the freshwater turtle, Pseudemys scripta, were estimated by characterizing geniculate afferents and the morphology of neurons in the visual cortex. Horseradish peroxidase injections in the thalamus revealed thin and unmyelinated terminal arbors that run horizontally from lateral to medial across the cortex, forming en passant synapses across the dendrites of cortical neurons. Axons with two calibers were seen, one with diameters between 0.5 and 2.0 μm, and a second with diameters below the resolution limit of the light microscope. The conduction velocity of geniculate afferents in the cortex was measured at 0.18 m/sec ±0.04 using the latency of extracellular field potentials evoked by electrical stimulation of the lateral forebrain bundle. The positions and dendritic arbors were characterized in Golgi preparations. Seven morphologically distinct neuron types were positioned to intersect the geniculate afferents in Golgi preparations. The spatial overlap between the dendritic arbors of these cells and the geniculate afferents varied from 128 to 850 μm. Temporal dispersion windows for the seven cell types ranged from 0.7 to 4.7 msec, estimated using a geniculate fiber conduction velocity of 0.18 m/sec. Estimated conduction velocities of 0.04 m/sec for small-caliber fibers produce temporal dispersion windows of 3.2 to 21.3 m/sec.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    International journal of primatology 18 (1997), S. 297-298 
    ISSN: 1573-8604
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Morphology 152 (1977), S. 247-279 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The intrinsic organization of medial cortex in snakes, primarily of the genera Natrix and Boa, was studied using Golgi and electron microscopic techniques. The area has three distinct layers, each containing a characteristic population of neurons. Stellate cells comprise a relatively small population of neurons with their somata and dendrites restricted to layer 1, the most superficial layer. Their axons course horizontally in layer 1. Candelabra cells form the largest population of neurons in medial cortex. Their somata lie densely packed in layer 2 and are joined by specialized junctions. Ascending dendrites extend from the somata into layer 1. They consist of spine-free proximal segments and spine bearing distal segments. Descending dendrites extend from the somata into the upper half of layer 3. The proximal segments bear few spines but branch into several tapered, distal segments which have a moderate covering of spines. One or two axons originate from the descending dendrites and descend through layer 3. The axons bear collaterals in the deep half of layer 3 and eventually bifurcate in the alveus. The medial branches run into the septum; the lateral branches course through other cortical areas. The axons bear frequent varicosities within medial cortex. Periventricular cells lie in the deep half of layer 3, either singly or in clusters. Their ascending dendrites extend radially into layer 1 where they branch into distal segments which resemble those of the candelabra cells. Their descending dendrites arborize horizontally in the alveus and bear a moderate covering of spines. Ependymal cells line the ventricular surface and send radial processes through the area's depth bearing lamellate processes.
    Additional Material: 25 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Morphology 168 (1981), S. 189-227 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The neural organization of the olfactory system in the desert iguana, Dipsosaurus dorsalis, has been investigated by using the Fink-Heimer technique to trace the efferents of the main and accessory olfactory bulbs, and Golgi preparations to determine the spatial relations between olfactory afferents and neurons in the primary olfactory centers.The accessory olfactory bulb projects to the ipsilateral nucleus sphericus via the accessory olfactory tract. The main olfactory bulb projects to the ipsilateral telen-cephalon via four tracts. The medial olfactory tract projects to the rostral continuation of medial cortex and to the septum. The intermediate olfactory tract projects to the olfactory tubercle and retrobulbar formation. The lateral olfactory tract projects to the rostral part of lateral cortex. The intermediate and lateral olfactory tracts also merge caudally to form the stria medullaris, which crosses the midline in the habenular commissure and distributes fibers to the contralateral hemisphere via two tracts. The lateral corticohabenular tract terminates in the contralateral lateral cortex. The anterior olfactohabenular tract terminates in the contralateral olfactory tubercle, retrobulbar formation and septum.The relation of olfactory afferents to neurons in the medial cortex, lateral cortex, nucleus sphericus, and septum corresponds to a pattern of organization that is typical of many olfactorecipient structures. Such structures are trilaminar, with neurons whose somata are situated in the intermediate layer (layer 2) sending spine-laden dendrites into an outer, molecular layer (layer 1). Olfactory afferents intersect the distal segments of these dendrites. By contrast, other olfactorecipient structures in Dipsoaurus deviate from the familiar pattern. Olfactory afferents intersect somata lying in layer 2 of the retrobulbar formation. Olfactory afferents include some fibers which course perpendicularly to the surface of the olfactory tubercle and extend deep to layer 2.
    Additional Material: 22 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Morphology 161 (1979), S. 185-210 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The cellular populations present in dorsomedial cortex in the snakes Constrictor constrictor, Natrix sipendon and Thamnophis sirtalis are described at the light microscopic level using Nissl and Golgi preparations as well as at the ultrastructural level. This area plays a central role in cortical organization in snakes by participating in major commissural and association projections.Systematic analyses of Golgi preparations indicate that five populations of neurons are present in dorsomedial area and have a preferential laminar distribution. Layer 1 stellate cells have somata positioned in the center of the outermost cortical layer, layer 1. Their dendrites are confined to this layer. Double pyramidal cells have their somata loosely packed in layer 2. Their dendrites bear a moderate population of spines, ascending through layer 1 to the pial surface and descending partially through layer 3. Some double pyramidal cells have somata displaced downwards into the upper third of layer 3. These neurons closely resemble the layer 2 double pryamidal cells. Layer 3 stellate cells have somata positioned in the middle third of layer 3. Their dendrites extend in all directions throughout layer 3 and through layer 2 into layer 1. Finally, horizontal cells have their somata positioned deep in layer 3, near the ventricle, and dendrites aligned concentric with the ventricle.Comparison of the organization of the known afferents to dorsomedial area with the distribution of the five cell types suggests that the laminations of both afferent fibers and dorsomedial neurons places specific neuronal populations in synaptic contact with specific sets of afferents.
    Additional Material: 21 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Morphology 165 (1980), S. 85-116 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Lateral cortex is the most laterally placed of the four cortical areas in snakes. Earlier studies suggest that it is composed of several subdivisions but provide no information on their organization. This paper first investigates the structure of lateral cortex in boa constrictors (Constrictor constrictor), garter snakes (Thamnophis sirtalis), and banded water snakes (Natrix sipedon) using Nissl and Golgi preparations; and secondly examines the relation of main olfactory bulb projections to the subdivisions of lateral cortex using Fink-Heimer and electron microscopic preparations.Lateral cortex is divided on cytoarchitectonic grounds into two major parts called rostral and caudal lateral cortex. Each part is further divided into dorsal and ventral subdivisions so that lateral cortex has a total of four subdivisions: dorsal rostral lateral cortex (drL), ventral rostral lateral cortex (vrL), dorsal caudal lateral cortex (dcL) and ventral caudal lateral cortex (vcL). Systematic analyses of Golgi preparations indicate that the rostral and caudal parts each contain distinct populations of neurons. Rostral lateral cortex contains bowl cells whose dendrites arborize widely in the outer cortical layer (layer 1). The axons of some bowl cells can be traced medially into dorsal cortex, dorsomedial cortex and medial cortex. Caudal lateral cortex contains pyramidal cells whose somata occur in layers 2 and 3 and whose dendrites extend radially up to the pial surface. In addition, three populations of neurons occur in both rostral and caudal lateral cortex. Stellate cells occur in all three layers and have dendrites which arborize in all directions. Double pyramidal cells occur primarily in layer 2 and have dendrites which form two conical fields whose long axes are oriented radially. Horizontal cells occur in layer 3 and have dendrites oriented concentric with the ependyma. Fink-Heimer preparations of snakes which underwent lesions of the main olfactory bulb show that the primary olfactory projections to cortex are bilateral and restricted precisely to rostral lateral cortex. Electron microscopic degeneration experiments indicate that the olfactory bulb fibers end as terminals which have clear, spherical vesicles and asymmetric active zones. The majority are presynaptic to dendritic spines in outer layer 1.These studies establish that lateral cortex in snakes is heterogeneous and contains two major parts, each containing two subdivisions. The rostral and caudal parts have characteristic neuronal populations. Primary olfactory input is restricted to rostral lateral cortex and seems to terminate heavily on the distal dendrites of bowl cells. Axons of some of these cells leave lateral cortex, so that the rostral lateral cortex forms a direct route by which olfactory information reaches other cortical areas. The functional role of caudal lateral cortex is not clear.
    Additional Material: 18 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Morphology 179 (1984), S. 153-174 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The anterior dorsal ventricular ridge was examined in the American alligator, Alligator mississippiensis, with cresyl violet and Golgi-Kopsch preparations. Four cytoarchitectonic areas (lateral dorsolateral, medial dorsolateral, intermediolateral, and lateral) can be distinguished by variations in the density of neurons and their tendency to form clusters of neurons with apposed somata. Three distinct types of neurons are distributed throughout these areas. Juxtaependymal neurons lie near the ventricular surface and have dendritic fields paralleling the ependymal layer. Their dendrites bear a moderate density of spines. Spiny neurons all have stellate shaped dendritic fields and dendrites that bear dendritic spines, but they vary greatly in the density of spines and the thickness of their dendrites. A very spiny variety has a high spine density and relatively thick dendrites. A moderately spiny variety has a moderate spine density and thin dendrites. A sparsely spiny variety has a low spine density and thick dendrites. Aspiny neurons have a relatively large number of dendrites that form a gnarled dendritic field and lack spines.
    Additional Material: 17 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Morphology 184 (1985), S. 135-154 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The dorsal ventricular ridge is a subcortical structure receiving sensory information from the thalamus in reptiles. In the red-eared turtle, Pseudemys scripta elegans, it contains four cytoarchitectonic areas each characterized by distinct thalamic projections. This is an electron microscopic study of one of these, the dorsal area, which receives its thalamic input from the tectorecipient nucleus rotundus. It contains four concentric zones, internal to the ependymal zone, each of which is distinguished by the distribution of spiny and aspiny neurons.The ependymal zone of dorsal area contains tanycytes whose tails extend into zones 2 and 4. Synapses, usually with asymmetric junctional complexes and round synaptic vesicles, occur on these processes. Zone 1 neurons have fusiform somata and dendrites that parallel the ventricular surface. Their cytoplasm contains rough endoplasmic reticulum located primarily in Nissl bodies, lipofuchsin granules, multivesicular bodies, extensive arrays of Golgi apparatus, and large numbers of mitochondria. Synapses occur mainly on dendritic spines and shafts of zone 1 neurons and less frequently on somata. The majority have round vesicles and asymmetric junctional complexes. In contrast to those in zone 1, neurons in zones 2 and 4 have large amounts of rough endoplasmic reticulum, giving their cytoplasm an electron-dense quality. Synapses occur mainly on spines and shafts of zone 2 and 4 neurons. As in zone 1, the majority have round synaptic vesicles and contain asymmetric junctional complexes. Zones 2 and 4 contain clusters of neurons distributed among isolated neurons. The clusters are larger and less frequent in zone 2. Protoplasmic and fibrous glial processes, axon boutons, dendrites, and axon fascicles surround the neuron clusters. Though less numerous, the same structures also occur inside the clusters. Most synapses inside the clusters have round synaptic vesicles, asymmetric junctional complexes, and occur mainly on spines. Some neurons in clusters have somata whose plasma membranes are in direct apposition. In contrast to dorsal ventricular ridge in snakes, no specialized intercellular contacts were seen between somata in clusters.
    Additional Material: 14 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Morphology 148 (1976), S. 1-21 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Anterior dorsal ventricular ridge (ADVR) is a major subcortical; telencephalic nucleus in snakes, Its structure was studied in Nissl, Golgi, and electron microscopic lrerarations in several species of snakes. Neurons in ADVR form a homogeneous population. They have large nuclei, scattered cisternae of rough endoplasmic reticulum in their cytoplasm, and bear dendrites from all portions of their somata. The dendrites have a moderate covering of pedunculated spines. Clusters of two to five cells with touching somata can be seen in Nissl, Golgi, and electron microscopic preparations. The area of apposition may contain a series of specialized junctions which resemble gap junctions. Three populations of axons can be identified in rapid Golgi preparations of snake ADVR. Type 1 axons course from the lateral forebrain bundle and bear small varicosities about 1 μ long. Type 2 axons arise from ADVR neurons and bear large varicosities about 5 μ. long. The origin of the very thin type 3 axons is not known; they bear small varicosities about 1 μ. long. The majority of axon terminals in ADVR are small (1 μ. to 2 μ long), contain round synaptic vesicles, and form asymmetric active zones. This type of axon terminates on dendritic spines and shafts and on somata. A small percentage of terminals are large, 5 μ in length, contain round synaptic vesicles, and form asymmetric active zones. This type of axon terminates only on dendritic spines. A small percentage of terminals are small, contain pleomorphic synaptic vesicles, and form symmetric active zones. This type of axon terminates on dendritic shafts and on somata.
    Additional Material: 15 Ill.
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