Tail skin of the dipnoan Neoceratodus larva: fine structure and differentiation

The fine structure of the tail skin oflarval Neoceratodusforsteri , between stages 40 and 50 (Kemp, 1982), is described and where applicable specific cellular components are compared and contrasted with comparable ones in the skin of adult dipnoans, teleosts and larval and adult amphibians.
The epidermis of the early developing tail, within the range studied, differentiates a variety of different cell types. Surface epithelial lucent and vacuolated lucent cells and basal cells are distinguished, and goblet (mucous) cells, Merkel cells and macrophages appear in the epidermis towards the end of the series.
Below a poorly developed collagenous basement lamella, immature melanophores with premelanosomes are present, and likewise there are non–myelinated nerves, some striated muscle fibres, capillaries and mesenchymal fibroblasts.
The tail epidermis is innervated by naked neurites from the beginning of the series, and the earliest recognizable Merkel cell is in synaptic association with neurites.     

Prey selection by the dobsonfly larva, Protohermes grandis (Megaloptera: Corydalidae)

SUMMARY 1. Prey selection by the dobsonfly larva, Protohermes grandis (Thunberg), was studied in stony riffles of the Yataro River, central Japan. The density, size distribution and taxonomic composition of available prey were assessed for 2 years. In order to know the encounter rate between prey and this ambush predator, prey mobility was also estimated from patterns of colonization of experimentally detiuded stones.
2. Foregut analyses revealed that maximum size of prey eaten increased with larval size, and large larvae did not take the smallest prey in spite of high availability in all seasons.
3. Charnov's (1976) optimal diet model quantitatively predicted such size-selective feeding under seasonally fluctuating conditions of water temperature and prey availability. Larvae maximized the feeding rate by selecting prey.
4. Maximum width of prey eaten coincided approximately with larval mandible length. Mandible size seemed to play an important role in the selection of prey in the optimal size range.     

The fine structure of the newly discovered propodial ganglia of the veliger larva of the nudibranch Onchidoris bilamellata

Summary Two pairs of ganglia are found in the propodial region of the veliger of Onchidoris bilamellata: the anterolateral pair is located at the foremost corners of the propodium, and the frontal pair is located beside the propodial midline. Both sets of ganglia are positioned below the epidermis, and they are joined to the cerebral ganglia by large, common connectives. Each ganglion possesses sensory cells, nerve cells and sheath cells, and the frontal pair contains a complement of secretory cells. Externally, the propodial ganglia are manifested as sensory fields. The fields of the anterolateral pair are elliptical in shape, and each appears as a band of cilia bordering an unciliated zone. The region devoid of cilia is composed of ordinary epidermal cells, whereas the ciliated portion is comprised of dendritic endings originating from cells in the ganglion. Dendrites arise from one type of sensory cell and pass through the epidermis in bundles. Each dendrite terminates as a single cilium at the epidermal surface. Sensory fields of the frontal ganglia are key-shaped and oppose one another on the anterior end of the foot. Each field appears as a flat, circular, unciliated region which extends into a ciliated groove that runs dorsally toward the mouth. The groove contains the terminals of secretory cells, ciliated sensory cells, and the cell bodies of nonciliated sensory cells. The nonciliated sensory cells, characterized by a microvillous apex, are the dominant cells in the flattened circular zone. The space between the frontal ganglia and the epidermis is bridged by bundles of processes which are similar to those of the anterolateral ganglia. However, these tracts contain collections of the apical processes of secretory cells, the dendrites of ciliated sensory cells, and the axons of nonciliated sensory cells. Morphological and behavioral evidence indicates that the propodial ganglia serve a chemosensory function during settlement and metamorphosis.     

Radio tracking and activity monitoring of the dobsonfly larva,Protohermes grandis (Megaloptera: Corydalidae)

Summary A miniature crystal-controlled radio transmitter, 7x17x2 mm³ and 185 mg in water, was attached to the back of prothorax of individual dobsonfly larvae, Protohermes grandis. Positions of these larvae in the stream bed were determined using a loop antenna, and they were tracked for 19 days. Actograms were also taken by recording the frequency variation of transmitting signals which were changed according to the larval posture. Larvae changed their positions in the stream bed in some nights, but never in the daytime. However, in most nights (92.7%), they continued to stay at the same position. Actograms revealed that larvae were quite motionless in most time (90.8% of daytime and 89.7% of night). Thus, larvae use the ambush mode of foraging in the central part of riffles where prey are continuously redistributed and sufficient oxygen is supplied with a water current.     

Seasonal change in the respiration of the dobsonfly larva, Protohermes grandis(Megaloptera: Corydalidae)

SUMMARY 1. Seasonal change in the respiration of the dobsonfly larva, Protohermes grandis ,was studied by measuring the oxygen consumption rate (resting metabolism) bimonthly for 2 years. The respiratory rate of the larva was significantly lower during the summer season when the stream temperature rose to 30°C.
2. Summer depression of respiration was confirmed by measuring the rate of carbon dioxide evolution. The mean value of the respiratory quotient was estimated to be 0.76 ± 0.05 SE. The larva is believed to conserve energy by this reduction in respiratory rate,
3. In other seasons, however, the larva maintained a higher respiratory rate and remained active even in the winter when the stream temperature decreased near to 0°C. In fact, significant growth in weight occurred from mid-October to late March.
4. This acclimation to temperature may enable the efficient allocation of energy during the long larval period (3 years) in streams which have large annual fluctuations in temperature.     

Dorsal longitudinal stretch receptor of Drosophila melanogaster larva - fine structure and maturation

Insects possess two types of sensory neurons: ciliated type I sensory neurons that innervate external sensory organs and chordotonal organs, and type II sensory neurons that form a subepidermal plexus or innervate stretch receptors. Among stretch receptors, a dorsel longitudinal stretch receptor is highly conserved in insects, being found in all insect orders investigated. Here we describe the topology and anatomical structure of this receptor in the fruit fly embryo and larva using transmission electron microscopy and single cell staining for fluorescence microscopy. The receptor is composed of the dorsal bipolar dendrite neuron, which arises from an archetypal cell lineage, its sister glial cell and the peripheral glial cell accompanying the nerve. The neuron is situated among the muscles in the dorsal body wall on the intersegmental nerve. Its two dendrites stretch the length of the segment to the segmental folds. The neuron is wrapped by both glial cells and surrounded by a common basal lamina, which fans out at the dendritic tips to attach them to the epidermal cells at the segmental borders.     

Fine structure of the dorsal ocellus of the worker honeybee

The three dorsal ocelli of worker honeybees have been studied by light and electron microscopy. Each ocellus has a single flattened spheroidal lens and about 800 elongated retinular cells. Retinular cells are paired and form a two-part plate-like rhabdom between their distal processes. Each rhabdomere comprises parallel microvilli projecting laterally from the apposed retinular cells. Primary receptor cell axons synapse within the ocellus with ocellar nerve fibers of two different calibers. Each ocellus has eight thick fibers ca 10 m?m in diameter and several thinner ones less than 3 m?m in diameter. Fine structural evidence suggests that retinular axons end presynaptically on both types of ocellar nerve fibers. Since all retinular cells apparently synapse repeatedly with the thick fibers this involves a convergence of about 100:1. Thick fibers always terminate postsynaptically within the ocellus while thin fibers terminate presynaptically on other thin fibers, thick fibers or retinular axons. Structural evidence for synaptic polarization indicates that retinular cells and thick fibers are afferent, thin fibers efferent. Thus complex processing of the ocellar visual input can occur before the secondary neurons of the three ocelli converge to form the single short ocellar nerve which runs to the posterior forebrain.     

Structure of ocellus photoreceptors in the ascidian Ciona intestinalis larva as revealed by an anti-arrestin antibody

Although there have been several studies on the structure of the ocellus photoreceptors in ascidian tadpole larvae using electron microscopy, the overall structure of these photoreceptor cells, especially the projection sites of the axons, has not been revealed completely. The number of photoreceptor cells is also controversial. Here, the whole structure of the ocellus photoreceptors in the larvae of the ascidian Ciona intestinalis was revealed by using an anti-arrestin (anti-Ci-Arr) antibody. The cell bodies of 30 photoreceptor cells covered the right side of the ocellus pigment cell and their outer segments extended through the pigment cell into the pigment cup. The axons of the photoreceptor cells were bundled together ventro-posteriorly in a single tract extending towards the midline. The nerve terminals diverged antero-posteriorly at the midline of the posterior sensory vesicle (SV). The Ci-arr gene was expressed throughout the SV at the embryonic mid-tailbud stage and it became restricted to the neighborhood of the ocellus pigment when ocellus pigmentation occurred. At the same time, the Ci-Arr protein was first detected, suggesting that the photoreceptor cells began to differentiate. The development of photoreceptor cells after hatching was also investigated using the anti-Ci-Arr antibody. Three hours after hatching, the photoreceptor terminals began to ramify and then expanded. Previous behavioral analysis showed that the larvae did not respond to the step-down of light until 2 h after hatching and then the photoresponse became robust. Accordingly, our results suggest that growth of the photoreceptor terminal is critical for the larvae to become photoresponsive.     

The surface fine structure of the ependymal lining of the lateral ventricle in rats with hereditary hydrocephalus

Summary The ependyma of the lateral ventricle of rats with hereditary hydrocephalus was studied using scanning electron microscopy. Normal rats from the same litters were used as control animals. The surface morphology of the lateral ventricle of normal rats corresponded to results reported by other authors. The most prominent changes in the surface morphology of the ependyma of the hydrocephalic rats were seen in the cilia. They were shortened, fewer in number and clumped or matted. The surface of the ependymal cells was flattened and contained small, irregular projections. The number of large supraependymal cells, regarded as neurons, appeared to have diminished in the hydrocephalic rats. The number of supraependymal macrophages was greatly increased in these rats, suggesting the existence of an ependymitis. Send offprint requests to: College of Veterinary Medicine, Department of Anatomy and Embryology, Hämeentie 57, SF-00550 Helsinki 55, Finland Acknowledgement: This study was supported by a grant from the Sigrid Jusélius Foundation to S.T.     

The anatomy of the median ocellus of Limulus

Summary The median ocellus of Limulus consists of irregular groups of large photoreceptor cells which form a cup-shaped retina around the ocellar lens. Each group is surrounded and penetrated by guanophores and glia. The photoreceptor cells have extensive rhabdomeric regions, both along infoldings of cell membranes and between cells. Five-layered junctions occur between rhabdomeric microvilli. An occasional arhabdomeric (AR) cell is associated with a group of photoreceptors. Fine dendritic branches of the AR cell penetrate the rhabdomeric regions and form five-layered junctions with photoreceptor rhabdomeres. Axons of photoreceptor cells, and of at least some AR cells, gather at the proximal side of the cup to form an optic nerve.Supported in part by NIH EY00312 and EY00377.We would like to thank Dr. W. K. Stell, Dr. A. C. Bell, and Dr. W. H. Fahrenbach for their helpful discussions.     

The fine structure ofPhycomyces

Summary The cytological organization of the apices of sporangiophores and hyphae ofPhycomyces Blakesleeanus was studied by means of light- and electron microscopy. The sporangiophore apex in growth stage I contains a mass of cytoplasm in which is embedded a cluster of lipid globules. Within the plug several zones are differentiated by the grouping of organelles. These zones are not separated by membranes. The most apical zone is low in nuclei and vesicles but rich in mitochondria and dense bodies. Below this zone lies a compact group containing up to several hundred nuclei. Along the midline of the cell, below these nuclei, lies an ovoid region from which vesicles, nuclei and mitochondria are excluded. In this ovoid exclusion zone lies the cluster of lipid globules mentioned above. Lateral to the exclusion zone (i.e. in the peripheral region of the cell) the cytoplasm is rich in nuclei, mitochondria, dense bodies, and especially in developing autophagic vesicles. Of these vesicles, the most mature are found farthest from the cell apex. The region between the exclusion zone and the upper end of the cell's large central vacuole is occupied largely by mature, swollen autophagic vesicles. In addition to the zonal organization described above, microtubules are found to run along the cylindrical cell's axis at a distance from the cell wall, and extend to the extreme apex of the cell. Similar tubules occur in growing hyphae, together with dense bodies, and the hyphal apex contains non-autophagic vesicles that increase in size with distance from the hyphal tip. The hyphae lack the zonation shown by sporangiophore apices. Perinuclear masses of cisternae are described and related to the dictyosomes of higher plants. The findings are discussed in relation to the function of the apices in tip growth and sporulation.This work was supported in part by a National Science Foundation Graduate Fellowship to the author, and in part by grant No. GB 3241 from the National Science Foundation to ProfessorKenneth V.Thimann.     

The fine structure of amylopectin

A critical examination of an enzymic method for determining the ratio of A and B chains in amylopectin leads to a value of ～ 1:1, and not 2:1 as suggested other workers. Partial debranching with pullulanase gave results consistent with earlier suggestions that A chains are predominantly and selectively removed. The ratio of A and B chains in a partially branched amylopectin has been determined, and the results are discussed in relation to possible structures for amylopectin.     

The fine structure of neurons

1. Thin sections of representative neurons from intramural, sympathetic and dorsal root ganglia, medulla oblongata, and cerebellar cortex were studied with the aid of the electron microscope. 2. The Nissl substance of these neurons consists of masses of endoplasmic reticulum showing various degrees of orientation; upon and between the cisternae, tubules, and vesicles of the reticulum lie clusters of punctate granules, 10 to 30 mmicro in diameter. 3. A second system of membranes can be distinguished from the endoplasmic reticulum of the Nissl bodies by shallower and more tightly packed cisternae and by absence of granules. Intermediate forms between the two membranous systems have been found. 4. The cytoplasm between Nissl bodies contains numerous mitochondria, rounded lipid inclusions, and fine filaments.