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Cytoskeletal architecture and immunocytochemical localization of fodrin in the terminal web of the ciliated epithelial cell.

In order to understand the cytoskeletal architecture at the terminal web of the ciliated cell, we examined chicken tracheal epithelium by quick-freeze deep-etch (QFDE) electron microscopy combined with immunocytochemistry of fodrin. At the terminal web, the cilia ended into the basal bodies and then to the rootlets. The rootlets were composed of several filaments and globular structures attached regularly to them. Decoration with myosin subfragment 1 (S1) revealed that some actin filaments ran parallel to the apical plasma membrane between the basal bodies, and other population traveled perpendicularly or obliquely, i.e., along the rootlets. Some actin filaments were connected to the surface of the basal bodies and the basal feet. Among the basal bodies and the rootlets there existed three kinds of fine crossbridges, which were not decorated with S1. In the deeper part of the terminal web, intermediate filaments were observed between the rootlets and were sometimes crosslinked with the rootlets. Immunocytochemistry combined with the QFDE method revealed that fodrin was a component of fine crossbridges associated with the basal bodies. We concluded that an extensive crosslinker system among the basal bodies and the rootlets along with networks of actin and intermediate filaments formed a structural basis for the effective beating of cilia.

Actins↗

Dendritic orientation and laminar architecture in the rabbit auditory thalamus.

A laminar organization composed of the dendritic fields of principal neurons and afferent axonal arbors has been proposed as the anatomical substrate for the frequency map at several levels of the mammalian central auditory system, including the inferior colliculus and medial geniculate body (MGB). In contrast to the auditory thalamus in most mammals, the ventral division of the rabbit medial geniculate body (MGV) has cellular laminae visible in routine Nissl stains, allowing a direct comparison of the laminar organization with the dendritic architecture and frequency organization. In total 30 presumptive relay neurons in the MGV were labeled with the juxtacellular recording method, and their dendritic arbors were fully reconstructed from serial sections with the aid of a computer microscope. The spatial organization of MGV dendritic fields was analyzed using the dendritic prism, dendritic stick, and fan-in projection methods. Quantitative spatial analyses revealed that, for MGV neurons in the central pars lateralis subdivision, the major axis of the dendritic fields (approximately 29 degrees relative to the horizontal plane) was closely aligned with that of the Nissl laminae (approximately 25 degrees). Both were oriented orthogonally to the tonotopic axis. In contrast, cells in the pars ovoidea had their major axis of orientation parallel to the anteroposterior axis of the brain. Although a bitufted dendritic field was the norm, it was not uncommon for MGV neurons to have pronounced spatial asymmetries in their dendritic fields. A model is presented that incorporates cellular laminae and oriented dendritic growth to form frequency-related slabs within the MGV.

Animals↗

Layer V in cat primary auditory cortex (AI): cellular architecture and identification of projection neurons.

The cytoarchitectonic organization and the structure of layer V neuronal populations in cat primary auditory cortex (AI) were analyzed in Golgi, Nissl, immunocytochemical, and plastic-embedded preparations from mature specimens. The major cell types were characterized as a prelude to identifying their connections with the thalamus, midbrain, and cerebral cortex using axoplasmic transport methods. The goal was to describe the structure and connections of layer V neurons more fully. Layer V has three sublayers based on the types of neuron and their sublaminar projections. Four types of pyramidal and three kinds of nonpyramidal cells were present. Classic pyramidal cells had a long apical dendrite, robust basal arbors, and an axon with both local and corticofugal projections. Only the largest pyramidal cell apical dendrites reached the supragranular layers, and their somata were found mainly in layer Vb. Three types departed from the classic pattern; these were the star, fusiform, and inverted pyramidal neurons. Nonpyramidal cells ranged from large multipolar neurons with radiating dendrites, to Martinotti cells, with smooth dendrites and a primary trunk oriented toward the white matter. Many nonpyramidal cells were multipolar, of which three subtypes (large, medium, and small) were identified; bipolar and other types also were seen. Their axons formed local projections within layer V, often near pyramidal neurons. Several features distinguish layer V from other layers in AI. The largest pyramidal neurons were in layer V. Layer V neuronal diversity aligns it with layer VI (Prieto and Winer [1999] J. Comp. Neurol. 404:332--358), and it is consistent with the many connectional systems in layer V, each of which has specific sublaminar and neuronal origins. The infragranular layers are the source for several parallel descending systems. There were significant differences in somatic size among these projection neurons. This finding implies that diverse corticofugal roles in sensorimotor processing may require a correspondingly wide range of neuronal architecture.

Animals↗

Architecture and neurocytology of monkey cingulate gyrus.

Human functional imaging and neurocytology have produced important revisions to the organization of the cingulate gyrus and demonstrate four structure/function regions: anterior, midcingulate (MCC), posterior (PCC), and retrosplenial. This study evaluates the brain of a rhesus and 11 cynomolgus monkeys with Nissl staining and immunohistochemistry for neuron-specific nuclear binding protein, intermediate neurofilament proteins, and parvalbumin. The MCC region was identified along with its two subdivisions (a24' and p24'). The transition between areas 24 and 23 does not involve a simple increase in the number of neurons in layer IV but includes an increase in neuron density in layer Va of p24', a dysgranular layer IV in area 23d, granular area 23, with a neuron-dense layer Va and area 31. Each area on the dorsal bank of the cingulate gyrus has an extension around the fundus of the cingulate sulcus (f 24c, f 24c', f 24d, f 23c), whereas most cortex on the dorsal bank is composed of frontal motor areas. The PCC is composed of a dysgranular area 23d, area 23c in the caudal cingulate sulcus, a dorsal cingulate gyral area 23a/b, and a ventral area 23a/b. Finally, a dysgranular transition zone includes both area 23d and retrosplenial area 30. The distribution of areas was plotted onto flat maps to show the extent of each and their relationships to the vertical plane at the anterior commissure, corpus callosum, and cingulate sulcus. This major revision of the architectural organization of monkey cingulate cortex provides a new context for connection studies and for devising models of neuron diseases.

Animals↗

Organization of frontoparietal cortex in the tree shrew (Tupaia belangeri). I. Architecture, microelectrode maps, and corticospinal connections.

Despite extensive investigation of the motor cortex of primates, little is known about the organization of motor cortex in tree shrews, one of their closest living relatives. We investigated the organization of frontoparietal cortex in Belanger's tree shrews (Tupaia belangeri) by using intracortical microstimulation (ICMS), corticospinal tracing, and detailed histological analysis. The results provide evidence for the subdivision of tree shrew frontoparietal cortex into seven distinct areas (five are newly identified), including two motor fields (M1 and M2) and five somatosensory fields (3a, 3b, S2, PV, and SC). The types of movements evoked in M1 and M2 were similar, but M2 required higher currents to elicit movements and had few connections to the cervical spinal cord and distinctive cyto- and immunoarchitecture. The borders between M1 and the anterior somatosensory regions (3a and 3b) were identified primarily from histological analysis, because thresholds were similar between these regions, and differences in corticospinal neuron distribution were subtle. The caudal (SC) and lateral (S2 and PV) somatosensory fields were identified based on differences in architecture and distribution of corticospinal neurons. Myelin-dense modules were identified in lateral cortex, in the expected location of the oral, forelimb, and hindlimb representations of S2, and possibly PV. Evidence for a complex primate-like array of motor fields is lacking in tree shrews, but their motor cortex shares a number of basic features with that of primates, which are not found in more distantly related species, such as rats.

Animals↗

Functional localization and cortical architecture in the nine-banded armadilli (Dasypus novemcinctus mexicanus).

A functional map of the armadillo neocortex was produced by cortical stimulation and recording evoked potentials following somatic, auditory and visual stimuli. The results obtained were then correlated with the cortical architecture as revealed by Nissl, Golgi and myelin-stained sections. Cortex rostral to the supraorbital sulcus has a wide layer IV and is mostly silent, except for a motor eye field and a part of the tongue sensory region in its caudal part. Two types of motor-sensory cortex are present caudal to the supraorbital sulcus. Postsupraorbital I is mostly motor and has prominent pyramidal layers. Layer V is particularly well developed and in rostral sections its superficial zone is broken up into clusters similar to the solid "barrels" seen in layer IV of other species. Postsupraorbital II has less prominent pyramidal layers and layers II and III are organized into clusters. This region corresponds to the sensory area for the limbs and trunk and the partially overlapping (surface recordings) sensory and motor areas for head, snout and tongue. Digits and limbs are rostral to the trunk representation in both the sensory and motor "homunculi." Even though surface recording was employed, potentials evoked by visual stimuli could only be recorded from a small caudal area with a very thin layer IV. Although striate and peristriate areas appear similar in Nissl stained preparations, they can be readily differentiated in Weil stained sections. The stellate character of neurons in layer IV of the visual cortex is particularly apparent in Golgi material. Auditory evoked surface potentials were recorded from a broad oval region in the caudal lateral cortex which has a wide layer IV and aggregates of neurons in layers II and III. A Weil stain demonstrates inner and outer bands of Baillarger in this same region. The presumptive insular cortex is electrically silent to sensory stimulation and presents as a narrow band just dorsal to the rhinal fissure with indefinite cell lamination and little myelin.

Animals↗

Electron microscopic studies of serially sectioned cat spinal alpha-motoneurons. II. A method for the description of architecture and synaptology of the cell body and proximal dendritic segments.

The paper presents a method for ultrastructural analysis and description of neuronal architecture and synaptology of cat spinal alpha-motoneurons from complete series of consecutive ultrathin sections through the cell body and proximal parts of the dendrites. The method implies that sections are selected for analysis only at certain constant intervals in the series. The occurrence of boutons of different morphological types on the neuronal surface was expressed by their percentage covering of the neuronal membrane. The neuronal surface was divided into a number of compartments and the synaptic covering was calculated separately for each compartment. An interval of 6 micrometer between the sections was used for these calculations, and the obtained values for synaptic covering were found not to differ significantly from those obtained in controls at 3 micrometer intervals. The number and location of individual large boutons (C- and M-types) were studied at 3 micrometer section intervals, and the escape of boutons connected to this procedure was estimated from control observations at 1 micrometer intervals. It is concluded that detailed information on neuronal synaptology can be obtained with this method, which will be used in three subsequent studies on functionally identified and intracellularly stained cat alpha-motoneurons.

Animals↗

The architecture and some of the interconnections of the rat's amygdala and lateral periallocortex.

The connections between the cerebral cortex and amygdala were studied in the rat by means of silver degeneration techniques. To help define the sites of origin and termination of cortico-amygdaloid connections, the architecture of the cortex and the amygdala was studied in sections from normal brains stained for cells, fibers, acetylcholinesterase activity, and heavy metals (Timm staining). The amygdalopetal cortex on the dorsal and lateral surfaces of the rat brain is limited to a narrow strip of periallocortex that forms the dorsal wall and lip of the rhinal sulcus. Histochemical stains indicate that this cortex comprises several stages of cortical differentiation that are intermediate between the ventrally adjacent allocortices and the dorsally adjacent neocortices. The lateral periallocortex consists of two major divisions, the agranular insula (area 13) anteriorly, and a temporal agranular cortex (areas 35 and 36) posteriorly. The principal amygdaloid target for this cortex is the lateral nucleus. Anterior area 13 and posterior area 35 project to the anterior and posterior halves, respectively, of the medial division of this nucleus, while posterior area 13 and anterior area 35 projects to the lateral division of this nucleus. All divisions of periallocortex also send projections to a part of the putamen that surrounds the lateral half of the central nucleus. All of area 13 also sends efferents to the anterior part of the basal nucleus, while the anterior half of area 13 sends an additional projection to the central nucleus. Comparison of these data with those obtained in the cat and monkey suggests that a constant feature of eutherian brains is the existence of a subset of efferents from each of the four neocortical sensory systems that is routed so as to provide subcortical limbic structures with modality-specific information. The initial sequence in this sensorilimbic system consists of one or more modality-specific corticocortical relays that originate in the primary sensory cortices and terminate in one of four topographically adjacent, modality-specific areas of the insular and temporal cortices. These insular and temporal areas then each establish modality-specific connections within the amygdaloid complex. The final set of relays presumably comprises the connection that each of these amygdaloid areas makes with the autonomic and endocrine nuclei of the brain.

Amygdala↗

Neuronal architecture of the nucleus of the solitary tract in the hamster.

This study provides a scheme for subdividing the nucleus of the solitary tract of the hamster on the basis of cytoarchitectonic criteria, cell measurements, and neuronal cell types identified with the Golgi method. Reduced silver-stained sections revealed the feltlike neuropil that characterizes the nucleus of the solitary tract and were used to define the boundaries of the nuclear complex. Adjacent sections stained for Nissl substance revealed ten subdivisions, each with a characteristic neuronal architecture based on cell sizes, shapes, and packing density. Some subdivisions, e.g., the ventral and medial subnuclei, were identified at all rostrocaudal levels of the nuclear complex, while other subdivisions, e.g., the caudally located dorsolateral and ventrolateral subnuclei, were restricted to particular levels. Golgi preparations were counterstained for Nissl substance, thus allowing dendro- and cytoarchitecture to be compared directly. This material permitted the identification of a number of functionally relevant features of the neuronal constituents of the subdivisions. This approach, employing three cytological methods, has permitted the assembly of a detailed atlas of the nucleus of the solitary tract. The subdivisions of the present atlas have been compared with their likely counterparts identified in previous investigations of the mammalian nucleus of the solitary tract. In order to relate cytoarchitecture with primary afferent termination sites and to define the gustatory-recipient subdivisions, the differential relationships of the subdivisions with lingual afferent projections in the hamster are also described. The present parcellation scheme is intended to facilitate anatomical and physiological investigations of the types of circuits that compose the medullary gustatory and general visceral sensory systems.

Aging↗

Lateral magnocellular thalamic nucleus in rabbits: architecture and projections to cingulate cortex.

The lateral magnocellular nucleus (LM) contains the largest neurons in the rabbit thalamus, yet its cortical connections have not been described. This study evaluates the architecture, cingulate cortical connections, and spontaneous rate of neuronal discharges in LM. At its maximal mediolateral extent in coronal sections, LM underlies the laterodorsal and lateroposterior nuclei. It has a short medial and long lateral limb, both of which have high levels of cytochrome oxidase activity. On the basis of horseradish peroxidase and fluorescent dye injections, LM projects primarily to area 29 and posterior area 24. Projections to area 29d are topographically organized so that the medial limb of LM projects to rostral area 29d, mid levels of LM where the limbs join project to midlevels of area 29d and lateral parts of the lateral limb project to posterior area 29d. It is mainly the midportion of the lateral and medial limbs that projects to areas 29b and 29c. The anterior parts of these areas receive input from dorsal parts of LM, whereas posterior levels of these areas receive input from ventral LM. The midregion of LM also projects to caudal area 24. Injections of 3H-amino acids into area 29d anterogradely label neuronal processes in LM. Finally, single unit electrophysiological recordings from LM in halothane-anesthetized rabbits showed a unique pattern of spontaneous discharges. Over 70% of the LM neurons cycled through a number of different phases with a mean +/- S.E.M. peak discharge rate of 31 +/- 4.7 Hz. This high rate contrasts with the 17.6 +/- 3.2 Hz rate for neurons that maintained a constant rate of discharge and the 7.5 +/- 1.3 Hz rate of discharges for neurons in nuclei dorsal and ventral to LM. LM neurons are large, have high levels of cytochrome oxidase and spontaneous activity, and project extensively to the posterior cingulate cortex. These features suggest that LM neurons are highly active metabolically and may be fast conducting efferents to cingulate cortex.

Afferent Pathways↗

Fine structure and synaptic architecture of HRP-labelled primary afferent terminations in lamina IIi of the rat dorsal horn.

The fine structure and synaptic architecture of the afferent terminations in dorsal horn lamina II are studied using a combined light and electron microscopic procedure after anterograde labelling with horseradish peroxidase. Vibratome parasagittal sections, stained with heavy metal intensified diaminobenzidine after tracer application to the dorsal roots, were flat-embedded in Epon. The five types of labelled terminal arbors occurring in lamina IIi (Cruz et al., '87: J. Comp. Neurol. 261:221-236) were drawn and relocated in 5-microns sections cut serially from the thick sections. Ultrathin sections were then cut from the 5-microns sections so that the terminal fibers and swellings observed in the light microscope could be traced in the electron microscope. The flame-shaped arbors arose from fine myelinated stem fibers. Terminal strands generated large oval central terminals of type II synaptic glomeruli (CII), which established frequent axoaxonal contacts. Similar terminals have been labelled in the cat after tracer injections into hair-follicle fibers (Réthelyi et al., '82: J. Comp. Neurol. 207:381-393). The other four plexuses arose from unmyelinated stem fibers. The swarms of ultrafine boutons consisted of extremely thin terminal fibers generating very small, round, or polygonal glomerular terminals containing tightly packed agranular synaptic vesicles of variable size and one mitochondrion at best. The terminal strands of the bouquet plexus bore long and scalloped central varicosities of type I synaptic glomeruli (CI) with pleomorphic agranular vesicles and a relative abundance of dendroaxonal contacts. These features, together with the location in dorsal lamina IIi, suggest their belonging to the fluoride resistant acid phosphatase (FRAP)-reactive population. The boutons of the undulating fibers and those of the lateral plexus were, like those of the bouquets, scalloped and elongated rostrocaudally (CI), but contained a few large granular vesicles. The occurrence of the swarm, undulating, and lateral plexuses in ventral lamina IIi, which seems to lack FRAP or peptidergic terminals, suggests an origin from other, still unidentified neurochemical populations of fine primary afferents.

Animals↗

Dendritic architecture of nucleus ambiguus motoneurons projecting to the upper alimentary tract in the rat.

The motor innervation for palatal, pharyngeal, laryngeal, and esophageal muscles originates within the nucleus ambiguus. Although the viscerotopic organization of the upper alimentary tract in the nucleus ambiguus has been extensively studied, little information concerning the dendritic arborization of nucleus ambiguus motoneurons is available. The neural tracer cholera toxin-horseradish peroxidase, which is particularly effective at revealing dendrites of retrogradely labeled neurons, was used to determine the dendritic architecture and organization of nucleus ambiguus motoneurons. In 72 rats, cholera toxin-horseradish peroxidase in volumes of 1.0-18 microliters was directly applied under pressure to the musculature of various sites along the upper alimentary tract. Motoneurons innervating the soft palate, pharynx, cricothyroid muscle, and cervical esophagus were all found to have extensive dendrites that extended into the adjacent reticular formation with a distinct pattern for each muscle group. In contrast, the dendrites of motoneurons innervating the thoracic and subdiaphragmatic esophagus were confined to the compact formation of the nucleus ambiguus. Dendritic bundling within the confines of the nucleus ambiguus was prominent following injection of tracer into the soft palate, pharynx, and esophagus. The bundles were primarily oriented in a rostrocaudal direction. These data suggest that the extensive extranuclear dendritic arborization of motoneurons innervating the soft palate, pharynx, larynx, and cervical esophagus provide a wide ranging target for multiple central afferents that may be involved in the differential control of muscles that participate in multiple complex motor functions. The lack of extensive extranuclear dendrites of motoneurons innervating the distal esophagus suggest that they receive focused central afferents. The prominent bundling of dendrites within the nucleus ambiguus may provide for synchronization of motoneurons innervating a specific muscle and perhaps for synchronization of motoneurons innervating different muscles acting in sequence.

Animals↗

Limbic thalamus in rabbit: architecture, projections to cingulate cortex and distribution of muscarinic acetylcholine, GABAA, and opioid receptors.

Nuclei of the thalamus that project to cingulate cortex have been implicated in responses to noxious stimuli, cholinergic and motor functions. The rabbit limbic thalamus may play an important role in these functions, but has not been studied extensively in terms of its cytoarchitecture, the topographical organization of its cortical projections, and differential transmitter regulation of its subnuclei. Therefore, the architecture, projections to cingulate cortex, and radioligand binding were investigated in the anterior, ventral, lateral, and midline nuclei of rabbit thalamus. The anterior nuclei are highly differentiated because both the dorsal and ventral nuclei have parvicellular and magnocellular divisions. Fluorescent dyes were injected into cingulate cortex to evaluate limbic thalamocortical connections. The anterior medial, submedial, and parafascicular nuclei project primarily to anterior cingulate cortex, while they have small or no projections to posterior areas. The ventral anterior and ventral lateral nuclei have a significant projection to dorsal cingulate cortex, including areas 24b and 29d. Projections of the anterior ventral nucleus are topographically organized, since medial parts of the parvicellular division project to rostral area 29, and lateral parts project to caudal area 29. The lateral nuclei and the parvicellular and magnocellular divisions of the anterior dorsal nucleus project with progressively higher densities in the rostrocaudal plane of area 29. Finally, the magnocellular division of the anterior ventral nucleus projects almost exclusively to caudal and ventral area 29, i.e., granular retrosplenial cortex. Ligand binding studies employed coverslip autoradiography and single grain counting techniques. Muscarinic receptor binding was moderate for both pirenzepine and oxotremorine-M in the parvicellular anterior ventral nucleus, while in other nuclei, there was an inverse relationship in the binding for these ligands. Most notably, the anterior dorsal nucleus, which receives no cholinergic input, had very high oxotremorine-M and low pirenzepine binding, while the anterior medial nucleus, which receives a moderate cholinergic input, had the highest pirenzepine binding and very low oxotremorine-M binding. Muscimol binding to GABAA receptors was highest in the anterior ventral nucleus, while it was at moderate levels in the anterior dorsal and lateral nuclei. The binding of Tyr-D-Ala-Gly-MePhe-Gly-ol to mu opioid receptors and 2-D-penicillamine-5-D-penicillamine-enkephalin to delta opioid receptors were both high in the parvicellular and low in the magnocellular divisions of the anterior dorsal nucleus. The magnocellular division of the anterior ventral, the lateral dorsal, and the parafascicular nuclei had high mu opioid binding, while the lateral dorsal and lateral magnocellular nuclei had low levels of delta opioid binding.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

Dendritic architecture of hypoglossal motoneurons projecting to extrinsic tongue musculature in the rat.

The tracer, cholera toxin-horseradish peroxidase, was used to determine the dendritic architecture and organization of hypoglossal motoneurons in the rat. In 22 animals, the tracer was injected unilaterally into either the geniohyoid, genioglossus, hyoglossus, or styloglossus muscle. Within the hypoglossal nucleus, motoneurons innervating the extrinsic tongue muscles were functionally organized. Geniohyoid and genioglossus motoneurons were located within the ventrolateral and ventromedial subnuclei, respectively, while hyoglossus and styloglossus motoneurons were located within the dorsal subnucleus. Motoneurons located in all subnuclear divisions were found to have extensive dendrites that extended laterally into the adjacent reticular formation and medially to the ependyma. Less extensive extranuclear dendritic projections were found in the dorsal vagal complex and median raphe. Prominent rostrocaudal and mediolateral dendritic bundling was evident within the ventral subnuclei and dorsal subnucleus, respectively. Dendritic projections were also found extending inter- and intrasubnuclearly with a distinct pattern for each muscle. These data suggest that the varied and extensive dendritic arborizations of hypoglossal motoneurons provide the potential for a wide range of afferent contacts for, and interactions among, motoneurons that could contribute to the modulation of their activity. Specifically, the prominent dendritic bundling may provide an anatomic substrate whereby motoneurons innervating a specific muscle receive and integrate similar afferent input and are thus modulated as a functional unit. In contrast, the extensive intermingling of both inter- and intrasubnuclear dendrites within the hypoglossal nucleus may provide a mechanism for the coordination of different muscles, acting synergistically or antagonistically to produce a tongue movement.

Animals↗

Functional architecture of vestibular primary afferents from the posterior semicircular canal of a turtle, Pseudemys (Trachemys) scripta elegans.

Physiological studies in many vertebrates indicate that vestibular primary afferents are not a homogeneous population. Such data raise the question of what structural mechanisms underlie these physiological differences and what functional role is played by afferents of each type. We have begun to answer these questions by characterizing the architecture of 110 afferents innervating the posterior canal of Pseudemys scripta. We emphasize their spatial organization because experimental evidence suggests that afferent physiological properties exhibit significant spatial heterogeneity. The sensory surface of the posterior canal comprises paired, triangular hemicristae, which are innervated by two afferent types. Bouton afferents (66% of total afferents) are found over the entire sensory surface. They differ significantly in the shape and size of their collecting areas, number of boutons, soma size, and axon diameter; this morphological variation is systematically related to the afferent's spatial position. In addition, multivariate analyses suggest that bouton afferents may comprise two subtypes: alpha afferents have delicate processes and are found throughout the crista; beta afferents are more robust and are concentrated preferentially toward the canal center. Calyx-bearing afferents comprise two morphological subtypes: dimorphs (13% of total afferents) bear calyceal and bouton endings; calyceal afferents (21%) bear calyceal endings only. Both types occur exclusively in an elliptical region near the center of each hemicrista; their morphology varies with radial distance from the center of this elliptical region. Our data provide evidence that in Pseudemys: (1) the classical vestibular afferent types (bouton, calyx, dimorph) are structurally heterogeneous, and (2) their spatial sampling characteristics are highly structured and distinctive for each type. These spatial patterns may shed light on regional differences in physiological profiles of vestibular afferents, and they raise questions about the role of this spatial heterogeneity in signaling head movement.

Animals↗

Influence of molecular order on the local work function of nanographene architectures: a Kelvin-probe force microscopy study.

We report a Kelvin-probe force microscopy (KPFM) investigation on the structural and electronic properties of different submicron-scale supramolecular architectures of a synthetic nanographene, including extended layers, percolated networks and broken patterns grown from solutions at surfaces. This study made it possible to determine the local work function (WF) of the different pi-conjugated nanostructures adsorbed on mica with a resolution below 10 nm and 0.05 eV. It revealed that the WF strongly depends on the local molecular order at the surface, in particular on the delocalization of electrons in the pi-states, on the molecular orientation at surfaces, on the molecular packing density, on the presence of defects in the film and on the different conformations of the aliphatic peripheral chains that might cover the conjugated core. These results were confirmed by comparing the KPFM-estimated local WF of layers supported on mica, where the molecules are preferentially packed edge-on on the substrate, with the ultraviolet photoelectron spectroscopy microscopically measured WF of layers adsorbed on graphite, where the molecules should tend to assemble face-on at the surface. It appears that local WF studies are of paramount importance for understanding the electronic properties of active organic nanostructures, being therefore fundamental for the building of high-performance organic electronic devices, including field-effect transistors, light-emitting diodes and solar cells.

Journal Article↗

Effect of architecture on the tensile properties of triblock copolymers in a lamellar phase.

We have used self-consistent field theory to calculate the tensile moduli of triblock copolymers in lamellar microstructures prepared from linear and star architectures. The extensional moduli K(33) are the main contributors to the tensile moduli, and the contribution of K(U)33 (the internal energy contribution to K(33)) is the main component of the value of K(33). We find that the tensile moduli of ABC three-miktoarm star terpolymers are smaller than those of ABC linear triblock copolymers having identical components, presumably for two main reasons. First, for the ABC three-miktoarm star terpolymers, the contributions of K(U)33 are larger than those of the linear triblock copolymers; we attribute this phenomenon to the star terpolymers having smaller lamellar domain sizes at equilibrium relative to those of the linear triblock copolymers. Second, conformational entropies play an important role in affecting the tensile moduli, mainly because of the different degrees of freedom of the various chains. In contrast, the shear moduli contribute negligibly to the tensile moduli.

Journal Article↗

Performance analysis of a dual-buffer architecture for digital flow cytometry.

BACKGROUND: Most current commercial flow cytometers employ analog circuitry to provide feature values describing the pulse waveforms produced from suspended cells and particles. This restricts the type of features that can be extracted (typically pulse height, width, and integral) and consequently places a limit on classification performance. In previous work, we described a first-generation digital data acquisition and processing system that was used to demonstrate the classification advantages provided by the extraction of additional waveform features. An improved version of the system is discussed in this paper, focusing on dual-buffering to ensure increased pulse capture. A mathematical model of the system is also presented for performance analysis. METHODS: The second-generation system incorporates fast digitization of analog pulse waveforms, instantaneous pulse detection hardware, and a novel dual-buffering scheme. A mathematical model of the system was developed to theoretically compute the capture-rate performance. RESULTS: The capture rate of the system was theoretically analyzed and empirically measured. Under typical conditions, a capture rate of 8,000 pulses/s was experimentally achieved. CONCLUSIONS: Based on these results, the dual-buffer architecture shows great potential for use in flow cytometry.

Algorithms↗