Morphology and ultrastructure of the alimentary canal of the cicada Platypleura kaempferi (Hemiptera: Cicadidae)

The alimentary canal of cicada Platypleura kaempferi is described. It comprises the oesophagus, filter chamber, external midgut section and hindgut. The elongate oesophagus expands posteriorly, with its posterior end constricting to become a bulb. The filter chamber consists of two parts: a very thin sheath and a filter organ. The filter organ is composed of the anterior and posterior ends of the midgut (internal midgut section), and the internal proximal ends of the Malpighian tubules. The external midgut section differentiates into a collapsed sac and a midgut loop. The latter is divided into three distinct segments. The hindgut contains a dilated rectum and a long narrow ileum. The distal portions of the four Malpighian tubules are enclosed in a peritoneal sheath together with the distal ileum before reaching to the rectum. Ultrastructurally, the oesophagus and the hindgut are lined with a cuticle. The filter chamber sheath consists of cells with large irregular nuclei. Filamentous substances coat the microvilli of the cells of the internal midgut section. The posterior end of the midgut comprises two types of cells, with the first type of cells containing many vesicles and scattered elements of rough endoplasmic reticulum. The anterior and posterior segments of the midgut loop cells have ferritin‐like granules. The ileum cells have well‐developed apical leaflets associated with mitochondria. Accumulations of virus‐like particles enclosed in the membrane are observed in the esophagus, conical segment, mid‐ and posterior segments of the midgut loop.     

Morphological and ultrastructural characterization of the alimentary canal in larvae of Streltzoviella insularis (Staudinger) (Lepidoptera: Cossidae)

Streltzoviella insularis (Staudinger) is an important tree‐boring pest, that primarily damages Sophora japonica (Linnaeus) and Ginkgo biloba (Linnaeus), as well as other common species, at great economic cost to the urban landscape construction industry in China. In the present study, the alimentary canal morphology of S. insularis was observed using light microscopy, and its ultrastructure was investigated by scanning and transmission electron microscopy. The foregut of S. insularis can be divided into the pharynx, esophagus, crop, proventriculus, and cardiac valve. The well‐developed crop forms the longest section of the foregut. It is able to store large amounts of food and is lined with a monolayer of epithelial cells. Many sclerotized microspines occur on the surface of the anterior intima and there are dense spines on the posterior intima of the proventriculus. Epithelial cells of the midgut include columnar cells, goblet cells, and regenerative cells, but endocrine cells are absent. The hindgut consists of the pyloric valve, ileum, and rectum. There is no clear distinction between the ileum and colon. The intima surface of the pyloric valve carries many microspines, whereas the intestinal wall of the rectum is thin with well‐developed rectal pads. The rectal epithelial cells form a squamous monolayer. A cryptonephric excretory system is located in the hindgut. There are six spiral Malpighian tubules, in which a cellular layer on a basement membrane encloses a lumen. These results will provide the basis for further studies of the structure and function in S. insularis larvae.     

Anatomy and fine structure of the alimentary canal of the spittlebug Lepyronia coleopterata (L.) (Hemiptera: Cercopoidea)

The alimentary canal of the spittlebug Lepyronia coleopterata (L.) differentiates into esophagus, filter chamber, midgut (conical segment, tubular midgut), and hindgut (ileum, rectum). The filter chamber is composed of the anterior extremity of the midgut, posterior extremity of the midgut, proximal Malpighian tubules, and proximal ileum; it is externally enveloped by a thin cellular sheath and thick muscle layers. The sac-like anterior extremity of the midgut is coiled around by the posterior extremity of the midgut and proximal Malpighian tubules. The tubular midgut is subdivided into an anterior tubular midgut, mid-midgut, posterior tubular midgut, and distal tubular midgut. Four Malpighian tubules run alongside the ileum, and each terminates in a rod closely attached to the rectum. Ultrastructurally, the esophagus is lined with a cuticle and enveloped by circular muscles; its cytoplasm contains virus-like fine granules of high electron-density. The anterior extremity of the midgut consists of two cellular types: (1) thin epithelia with well-developed and regularly arranged microvilli, and (2) large cuboidal cells with short and sparse microvilli. Cells of the posterior extremity of the midgut have regularly arranged microvilli and shallow basal infoldings devoid of mitochondria. Cells of the proximal Malpighian tubule possess concentric granules of different electron-density. The internal proximal ileum lined with a cuticle facing the lumen and contains secretory vesicles in its cytoplasm. Dense and long microvilli at the apical border of the conical segment cells are coated with abundant electron-dense fine granules. Cells of the anterior tubular midgut contain spherical secretory granules, oval secretory vesicles of different size, and autophagic vacuoles. Ferritin-like granules exist in the mid-midgut cells. The posterior tubular midgut consists of two cellular types: 1) cells with shallow and bulb-shaped basal infoldings containing numerous mitochondria, homocentric secretory granules, and fine electron-dense granules, and 2) cells with well-developed basal infoldings and regularly-arranged apical microvilli containing vesicles filled with fine granular materials. Cells of the distal tubular midgut are similar to those of the conical segment, but lack electron-dense fine granules coating the microvilli apex. Filamentous materials coat the microvilli of the conical segment, anterior and posterior extremities of the midgut, which are possibly the perimicrovillar membrane closely related to the nutrient absorption. The lumen of the hindgut is lined with a cuticle, beneath which are cells with poorly-developed infoldings possessing numerous mitochondria. Single-membraned or double-membraned microorganisms exist in the anterior and posterior extremities of the midgut, proximal Malpighian tubule and ileum; these are probably symbiotic.     

The structure of the rectal pads of Periplaneta americana L. With regard to fluid transport

The rectum of Periplaneta americana L. is lined with cuticle and has six radially arranged cushion-shaped thickenings, the rectal pads, composed of columnar cells. Narrow strips of simple rectal cells lie between the pads. Tall junctional cells form a thin but continuous collar around the pads where they join the rectal cells. The epithelium is surrounded by a layer composed of circular and longitudinal muscles and connective tissue. This layer of muscle and connective tissue is innervated and tracheated, and is separated from the pad surface by a subepithelial sinus. Fluid flowing through the sinus enters the haemolymph through openings in the muscle layer whre large tracheae penetrate. These openings can be sealed by muscle contractions that appress the muscle around the openings against the pad surface. The tracheae pass on into the pads, following basement membrne-lined indentations of the pad surface. Within the pad tracheolar cells send fine branches between the cells. Near the apical and basal surfaces the lateral membranes of pad cells are bridged by septate desmosomes that form a continuous band around the cells. Between apical and basal septate desmosomes is an interconnected labyrinthine system of intercellular spaces. There are three kinds of space, dilations and apical sinuses, both of variable size, and narrow communicating channels about 200 Å wide. The membranes of the latter have mitochondria closely associated with them. Continuity between the system of spaces and the subepithelial sinus is established by the basement membrane-lined invaginations of the basal surface where tracheae penetrate between pad cells. Apical surfaces of the pad cells are highly infolded and are also associated with mitochondria. However, unlike the lateral membranes facing the narrow channels, the apical membranes have a cytoplasmic coating of particles. Both associations of mitochondria with membranes constitute discrete structural entities that are found in many transporting epithelia, and we have termed them “plasmalemma-mitochondrial complexes.” As the rectal pads are organized into systems of spaces that ultimately open in the direction of fluid movement, existing models of solute-coupled water transport can be applied. However, the rectal pads are structurally more complex than fluid-transporting tissues of vertebrates. This complexity may be related to the ability of the rectum to withdraw water from ion-free solutions in the lumen. We present a structural model involving solute recycling to explain the physiological characteristics of rectal reabsorption.     

The morphology of the phallosome and accessory gland material transfer during copulation in the blowfly,Lucilia cuprina (Insecta,Diptera)

Summary The mechanism of insemination in Lucilia cuprina is described. There are four duct openings on the phallosome. The terminal pore is continuous with the internal reproductive organs. The sub-terminal pore and paired, lateral pores are the openings of ducts formed by cuticular invaginations. The male accessory gland material appears to be re-routed from the terminal pore into the ducts of the lateral barbs once sperm transfer is complete. A novel means of deposition of the male accessory material is described, in which paired barbs on the phallosome tear the cuticle of thick-walled pads in the bursa copulatrix. After mating, accessory material is found within intra-cuticular spaces in the bursa copulatrix, which appear to become sealed at the points of penetration by plugs or scars.     

Microspine variation in hindgut regions of four families of cockroaches (Blattaria)

Microspines in the cockroach (Blattaria) hindgut were studied to determine their structure, variation, and potential use in classification. Short spines (1–10 μm) were found in all regions of the hindgut, except for the rectal cuticle in all species, the posterior region of the ileum and colon in C. punctulatus and the posterior portion of the ileum of the blaberoid species. They were also characteristics of the pyloric and other valvular cuticle between areas of the hindgut. Moderate (20–60 μm) and long (over 100 μm) microspinal lengths were associated with bacterial aggregations or plaques in the ileum. Microspinal modifications showed only poor phylogenetic correlations.     

合哑蝉成虫消化道形态、组织结构及超微结构（英文）

【目的】本研究通过合哑蝉Karenia caelatata成虫消化道的形态学、组织学和超微结构研究,进一步了解蝉科(Cicadidae)代表种类的消化道形态和功能分化。【方法】利用光学显微镜和透射电子显微镜技术,对合哑蝉雄成虫消化道的整体形态以及食道、滤室(中肠前端及后端、马氏管基部、后肠基部)、滤室外中肠(锥形体、中肠环)、后肠(回肠、直肠)的一般形态和超微结构进行了详细观察,同时对滤室的组织结构进行了研究。【结果】结果表明,合哑蝉消化道由食道、滤室、滤室外中肠及后肠组成。食道狭长,被有上表皮和内表皮。中肠前端、中肠后端、马氏管基部以及后肠基部被一肌肉鞘包围形成滤室构造。组成中肠前端和后端的细胞基膜高度内褶,顶端的微绒毛发达。中肠后端分布许多线粒体和高电子密度的分泌颗粒。滤室外的中肠包括膨大的锥形体、中肠环。其中,锥形体由两种细胞组成;中肠环分为前、中、后3个不同的区段。前中肠细胞包含大量的分泌颗粒、线粒体、粗面内质网和溶酶体;中中肠细胞含有分泌颗粒;后中肠细胞包括许多低电子密度的分泌颗粒和滑面内质网。类铁蛋白颗粒零星分布于中肠环的前、中区段。组成锥形体和中肠环前端的细胞顶端微绒毛被...     

Histologie und feinstruktur der larvalen kiemenkammer von Aeshna cyanea Müller (Odonata: Anisoptera)

Zusammenfassung Ein großer Teil des Rectums der Larven von Aeshna cyanea wird von der Kiemenkammer eingenommen. Hier ist das Epithel im Bereich der Kiemenstreifen modifiziert. Ein Kiemenstreifen besteht aus Haupt- und Querfalten. Basale Teile der Querfalten (Basalwülste) werden von Zellen gebildet, die morphologisch einem transportaktiven Epithel ähneln (unter der Cuticula apikaler Mikroleistensaum mit zahlreichen Mitochondrien, basales Labyrinth). Die aus zwei Basalwülsten hervorgehenden Kiemenblättchen, locker aufeinanderliegende, einschichtige Epithelien, zeigen Strukturmerkmale respiratorischer Epithelien (niedrige Zellen, reiche Tracheen- und Tracheolenversorgung in Invaginationen der basalen Plasmamembran, die bis nahe unter die Cuticula reichen). Man darf daher annehmen, daß diesem Enddarmabschnitt neben der Respiration auch ionentransportierende Tätigkeit zukommt.

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Histology and fine structure of the larval branchial chamber in Aeshna cyanea Miller (Odonata: Anisoptera)

Summary In larval Aeshna cyanea the anterior portion of the rectum has been modified into a branchial chamber with six gill folds (corresponding to the pads in the posterior rectal portion). A gill fold is made up of a longitudinal main fold with obliquely placed transverse folds at each side. Each transverse fold consists of two basal pads enclosing fat body cells. The cells of the basal pads show some details reminiscent of transporting epithelia (e.g. apical and basal infoldings, numerous mitochondria). The apical parts of the pads are constricted into lamellae projecting into the rectal lumen. These lamellae are typical respiratory epithelia, which consist of two very flat layers with extracellular tracheoles arranged in invaginations of the basal plasma membrane just beneath the cuticle. Thus it may be assumed that this part of the rectum is concerned with respiration as well as absorption of ions.

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Abkürzungen äE äußere Epicuticula - Bl Basallamelle - Bw Basalwulst - Cu Cuticula - cM circuläre Muskulatur - Dl Darmlumen - En Endocuticula - Fk Fettkörper - Gl Glykogen - hC homogene Cuticula - Hc Hämocoel - Hf Hauptfalte - iE innere Epicuticula (=dense layer) - Kb Kiemenblättchen - Ks Kiemenstreifen - Mi Mitchondrium - Mt Mikrotubuli - Mu Muskeln - Mvb Multivesikularörper - N Kern - Pi Pigmentgranum - Qf Querfalte - Re Rectumepithel - RER rauhes endoplasmatisches Reticulum - sL subcuticulare Lage - TR Trachee - Tr Tracheole Herrn Professor Dr. R. Altevogt, Münster, zum 50. Geburtstag gewidmet.     

On the fine structure of the creeping larva of Loxosomella murmanica: additional evidence for a clade of Kamptozoa (Entoprocta) and Mollusca

The creeping larva of the kamptozoan (entoproct) Loxosomella murmanica was investigated using transmission electron microscopy. The late larva exhibits a prominent apical organ connected to the ‘cerebral’ commissure of large cerebral ganglia, which supply the paired frontal organ. From the cerebral ganglia two paired nerve cords project backwards, closely resembling the tetraneuralian pattern of basal molluscs. In addition, a neural ring supplying the prototroch is present. The epidermis is composed of myoepithelial cells. Dorsally its cuticle is covered by granules of unknown composition. The prototroch consists of two ciliary rings; a downstream collecting system is not present. Although there is a one‐way gut with a lumen throughout, the larva obviously does not feed. A single pair of protonephridia is present. The foot sole shares distinct similarities with basic molluscs, particularly with those of the aplacophoran Solenogastres: The anterior part shows a huge, subepidermal pedal gland and several bundles of cirri consisting of compound cilia. The posterior part is ciliated with intraepithelial mucous cells interspersed. The dorsoventral muscle fibres show the mollusc‐like ventral intercrossing. The present results and previous findings, in particular the chitinous, non‐moulted cuticle, the sinus circulatory system, and a number of neural features shared by Kamptozoa and Mollusca, provide substantial evidence for a direct sister‐group relationship between these phyla. In addition, the basal position of the Solenogastres (Neomeniomorpha) within the Mollusca is corroborated.     

Light and electron microscopic study of the hindgut of the ant (Formica nigricans, hymenoptera): I. Structure of the ileum

The study of the ileum of the ant Formica nigricans by light and electron microscopy revealed the existence of three differentiated regions: proximal, middle, and distal ileum. The middle region constitutes most of the length of the organ. Its wall is made up by a folded simple epithelium lined by a cuticle, which is surrounded by an inner circular muscle layer and various external longitudinal muscle fibers adjacent to the hemolymph. A subepithelial space is present between the epithelium and the circular muscle layer. Epithelial cells show extensive infoldings of the apical, and to a lesser extent the basolateral plasma membrane. Apical infoldings are characterized by the presence of 10-nm particles (portasomes) covering the cytoplasmic side of the membrane. Mitochondria are abundant throughout the cytoplasm, although they mainly are present underneath the apical infoldings. Lateral borders of epithelial cells display an apical junctional complex, mainly constituted by a long and convoluted pleated septate junction. These features support the view that epithelial cells in the middle ileum are specialized in ion solutes and water transport. The proximal ileum connects with the ampulla into which the Malpighian tubules drain. As opposed to the middle ileum, epithelial cells of the proximal ileum show less developed basolateral infoldings, and the apical plasma membrane is devoid of portasomes and only occasionally invaginates. These features suggest that the proximal ileum plays no relevant role in ion and water transport. The distal ileum penetrates into the rectal sac, forming a valve-like structure; this region presumably controls the amount of urine reaching the rectum.     

Regulation of pattern formation in the Drosophila hindgut by wg, hh, dpp, and en

The hindgut of the Drosophila embryo is subdivided into three major domains, the small intestine, large intestine, and rectum, each of which is characterized by specific gene expression. Here we show that the expression of wingless (wg), hedgehog (hh), decapentaplegic (dpp), and engrailed (en) corresponds to the generation or growth of particular domains of the hindgut. wg, expressed in the prospective anal pads, is necessary for activation of hh in the adjacent prospective rectum. hh is expressed in the prospective rectum, which forms anteriorly to the anal pads, and necessary for the expression of dpp at the posterior end of the adjacent large intestine. wg and hh are also necessary for the development of their own expression domains, anal pads, and rectum, respectively. dpp, in turn, causes the growth of the large intestine, promoting DNA replication. en defines the dorsal domain of the large intestine, repressing dpp in this domain. A one-cell-wide domain, which delineates the anterior and posterior borders of the large intestine and its internal border between the dorsal and ventral domains, is induced by the activity of en. We propose a model for the gene regulatory pathways leading to the subdivision of the hindgut into domains.     

Ultrastructure of the rectum of infective-stage Wuchereria bancrofti (Nematoda: Filarioidea).

The authors have examined the ultrastructure of the rectum of infective-stage Wuchereria bancrofti by transmission electron microscopy. Our observations show that the rectum is divided into anterior and posterior segments. The cells of the anterior rectum appear to be derived from the microfilarial R (rectal) cells described by other authors. In both stages, these cells show voluminous nuclei, abundant mitochondria, and small cytoplasmic processes which contain fibrillar components. Amorphous material associated with these processes appears throughout the larval rectum and may protrude from the anus as the rectal plug. In the specimens examined, a patent lumen could not be traced completely through the anterior rectum. The posterior rectum has no counterpart in published accounts of microfilarial ultrastructure and probably arises during larval morphogenesis; it is lined with invaginated body cuticle, overlaid by a single layer of epithelial cells which may be of hypodermal origin.     

Gut morphology of Mastotermes darwiniensis Froggatt (Isoptera : Mastotermitidae)

The digestive system of Mastotermes darwiniensis (Isoptera : Mastotermitidae) is similar to that of other lower termites. The cuticle in the proventriculus of the foregut is sculptured into 6 large dentate plates. Large setae are dispersed over the 1st and 2nd order folds and small setae are on the 3rd order folds. Epithelial cells in the foregut are of one type. The midgut cells are of one functional type, with 3 stages of the developmental cycle clearly distinguishable at any one time. There is no close association of mitochondria with the apical plasmalemma or microvilli. The epithelium rests on a basal lamina and has regularly distributed regenerative crypts. The midgut cells contain a large number of mitochondria close to the basal plasmalemma. Invaginations of the basal plasmalemma are very extensive and small tracheoles are plentiful close to the basal lamina. The presence of rough endoplasmic reticulum, most of which exists in the supranuclear cytoplasm, indicates that protein synthesis occurs in these cells. An abundance of basal plasmalemma invaginations is indicative of some fluid transport occurring across the membranes. The malpighian tubules have accumulations of mineral concretion forms as well as glycogen. Tracheoles are fairly abundant and distributed around the tubules. Epithelial cells in the region where the malpighian tubules join the midgut contain granules which are presumed to be secretory. Dentate plates around the anterior colon entrance are oriented so as not to hinder the flow of the lumen contents towards the posterior colon. Invaginations of the apical plasmalemma of the normal paunch epithelial cell suggest that they are involved in fluid or solute uptake from the lumen. The cuticle of the hindgut consists of areas with adhering bacteria and areas showing an even distribution of pores free of bacteria. The epithelial cells of the anterior colon resemble those in the paunch. The epithelial cells of the posterior colon show 3 variations: a squamous-cuboidal cell with unconstricted lumen; a cuboidal-columnar cell type found at the constriction site close to the rectum; a second squamous-cuboidal cell type constituting the junction of the colon and the rectum. This last cell type shows an abundance of cytoplasmic microtubules and a thick subcuticular zone.     

Ultrastructure of osmoregulatory organs in larvae of the brackish-water mosquito,Culiseta inornata (Williston)

The ultrastructure of the Malpighian tubules, ileum, rectum, anal canal, and anal papillae of larvae of the mosquito Culiseta inornata was examined. The Malpighian tubules, rectum, and anal papillae have many of the ultrastructural features characteristic of ion transport tissues, i.e., elaboration of the basal and apical membranes and a close association of these membranes with mitochondria. The Malpighian tubules possess two cell types, primary and stellate. The larval rectum of C. inornata is composed of a single segment containing a homogenous population of cells. In this respect, the larval rectum of C. inornata is distinct from that of saline-water species of Aedes. The cells in the larval rectum of C. inornata, however, closely resemble those of one cell type, the anterior rectal cells, of the saline-water mosquito Aedes campestris with regard to cell and nuclear size, the percentage of the cell occupied by apical folds, and mitochondrial density and distribution. No similarities can be found between the rectum of C. inornata and the posterior segment of the saline-water Aedes, which functions as a salt gland. On this basis, we have postulated that the rectum of C. inornata does not function as a site of hyperosmotic fluid secretion. The ultrastructure of the anal papillae of C. inornata is consistent with a role in ion transport. The significance of these findings to comparative aspects of osmoregulatory strategies in mosquito larvae is discussed.     

Calcium translocations during the moulting cycle of the semiterrestrial isopod <Emphasis Type="Italic">Ligia hawaiiensis</Emphasis> (Oniscidea,Crustacea)

Terrestrial isopods moult first the posterior and then the anterior half of the body. During the moulting cycle they retain a significant fraction of cuticular calcium partly by storing it in sternal CaCO₃ deposits. We analysed the calcium content in whole Ligia hawaiiensis and the calcium distribution between the posterior, the anterior ventral, and the anterior dorsal cuticle during four stages of the moulting cycle. The results indicate that: (1) overall, about 80% of the calcium is retained and 20% is lost with the exuviae, (2) in premoult 68% of the calcium in the posterior cuticle is resorbed (23% moved to the anterior ventral cuticle, 17% to the anterior dorsal cuticle, and the remaining 28% to internal tissues), (3) after the posterior moult 83% of the calcium in the anterior cuticle is shifted to the posterior cuticle and possibly to internal storage sites, (4) following the anterior moult up to 54% of the calcium in the posterior cuticle is resorbed and used to mineralise the new anterior cuticle. ⁴⁵Ca-uptake experiments suggest that up to 80% of calcium lost with the anterior exuviae may be regained after its ingestion. Whole body calcium of Ligia hawaiiensis is only 0.7 times that of the fully terrestrial isopods. These terrestrial species can retain only 48% of whole body calcium, suggesting that the amount of calcium that can be retained by shifting it between the anterior and posterior integument is limited. We propose that fully terrestrial Oniscidea rely to a larger degree on other calcium sources like internal stores and uptake from the ingested exuviae.     

太白蝎蛉消化道形态学与组织学研究

利用光学显微镜和扫描电子显微镜, 在形态学和组织学水平上研究了太白蝎蛉Panorpa obtusa Cheng成虫消化道的结构。结果表明： 蝎蛉消化道由前肠、中肠、和后肠组成。前肠包括咽喉、食道、和前胃, 但没有嗉囊,其中咽喉可分为骨化的前咽和附着扩肌的后咽（咽喉唧筒）; 前胃壁很厚,内膜上长有许多排列整齐、紧密的棕色胃刺,司过滤、暂时储存和磨碎食物的功能; 前肠末端有6个贲门瓣伸入中肠。中肠较长且膨大,其肠壁细胞由柱状细胞和再生细胞组成; 肠壁细胞外分别为环肌和纵肌,无胃盲囊,也未观察到围食膜。6根棕红色的马氏管位于中、 后肠分界处。后肠分为不对称的“V”字型回肠、环状结肠、以及膨大透明的直肠, 直肠内壁上有6个交替排列的直肠垫。最后简要讨论了蝎蛉消化道的结构与功能,及其在蝎蛉科昆虫分类中的意义。     

The giant fiber system in the forelegs (whips) of the whip spider Heterophrynus elaphus Pocock (Arachnida: Amblypygi)

Summary The front legs of the whip spider H. elaphus are strongly modified to serve sensory functions. They contain several afferent nerve fibers which are so large that their action potentials can be recorded externally through the cuticle. In recordings from the tarsus 7 different types of afferent spikes were identified; 6 additional types of afferent spikes were discriminated in recordings from the tibia and femur. Most of the recorded potentials could be attributed to identifiable neurons serving different functions. These neurons include giant interneurons and giant fibers from diverse mechanoreceptors such as slit sense organs, trichobothria, and a joint receptor. In the present report these neurons are characterized using electrophysiological and histological methods. Their functions are discussed in the context of the animal's behavior.Abbreviations GN giant neuron - S segment     

Studies on the ultrastructure of the integument of the rotifer Habrotrocha rosa Donner (Aschelminthes)

Summary The integument of the rotifer Habrotrocha rosa Donner is provided with pores and formed by an extrasyncytial cuticle and a syncytial hypodermis. The hypodermis peripherally contains 3 layers of dense cytoplasm and borders the cuticle by an asymmetric cell membrane. The wall of the pores is stiffened proximally like an annulus. The pores lead into cytoplasmic invaginations which are surrounded by vesicles. Close to and also beneath the condensed cytoplasmic layers microbodies are found, which are interpreted as microperoxisomes. Subhypodermal layers of muscles are connected with the cytoplasm of the hypodermis by desmosome-like structures.I am indebted to Dr. H. Breucker, Anatomisches Institut Hamburg, and Prof. Dr. W. Becker, Zoologisches Institut Hamburg, under whose direction this work was carried out. Supported by the Deutsche Forschungsgemeinschaft (Be 464/10)     

Apple Fruit Cuticles and the Occurrence of Pores and Transcuticular Canals

Developmental studies were made on the dewaxed thin-sectionedapple fruit cuticles of 10 Malus sylvestris Mill, cultivarsfrom 4 weeks before anthesis through fruit maturation and harvest.Cuticular development appears to correlate well with the generalgrowth of the fruit. However, no correlation exists betweenfruit size and cuticle thickness. Cuticular pores were evidentas early as 1 week before anthesis and transcuticular canalsbecame evident by 1 week following anthesis. Dewaxed thin-sectioned,as well as isolated, mature fruit cuticles of 16 cultivars andfour crab-apples consistently revealed the distinct presenceof ubiquitous pores and canals. Evidence is provided by lightmicroscopy and scanning electron microscopy (SEM). Measurementswere taken of cuticle thicknesses during development and ofcuticular pore dimensions, and calculations were made of poreand canal numbers. Fruit size alone is not directly indicativeof total pore numbers per surface area. Canal lengths are directlyrelated to the developmental thickness of the cuticle. No correlationwas found between the thickness of the mature cuticle and eitherthe number of pores present or the pore diameters. Malus sylvestris Mill, apple fruit, morphology, cuticle, cuticular flanges, cuticular pores, transcuticular canals, ultrastructure     

The control of hindgut motility in the lobster,Homarus gammarus (L.)

1. The sixth abdominal ganglion (6 A.G.) of the lobster Homarus gammarus (L.) innervates the rectum via the paired posterior intestinal nerves (P.I.N.’s) and the paired anal nerves. The anterior branches of the P.I.N.’s supply the anterior hindgut, the main faecal expulsion region, whilst the posterior branches (P.I.N.p.’s) supply the posterior region and the 5 extrinsic radial muscle groups around the anus.

2. Stimulation of the ventral nerve cord (V.N.C.) or the oesophageal connectives initiates co‐ordinated hindgut movements, the defaecatory response. The nervous activity eliciting these movements passes down the P.I.N.’s. The anal nerves are devoid of motor function with respect to the hindgut.

3. In addition to neurogenic movements the rectum also undergoes non‐coordinated, low amplitude longitudinal and circular muscle contractions. These are thought to be due to independently acting endogenous oscillators within the muscles themselves. The radial muscles of the anus also exhibit rhythmical contractions after an initial maximal contraction following stimulation of the P.I.N.p.’s.

4. Receptors responding to anal dilation and closure have been shown to exist in the anal nerves. They are non‐specific soft cuticle receptors which are, apparently, positionally sensitive. These receptors are not thought to modulate motor output from the 6 A.G. to the rectum at the level of the 6 A.G.

5. Bifurcating motor axons are thought to exist in the P.I.N.’s.

6. It is concluded that the defaecatory response of the lobster is a centrally programmed phenomenon.