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.     

Fine Structure of the Midgut and Hindgut in Lepidocampa weberi (Insecta,Diplura)

The fine structure of the alimentary canal, especially the midgut and hindgut of Lepidocampa weberi (Diplura: Campodeidae) is described. The general organization of the canal is similar to that of Campodea. The midgut epithelium is composed of columnar apical microvillated cells. Each nucleus contains a single intranuclear crystal. Close to the pyloric region, the posterior midgut cells are devoid of microvilli and intranuclear crystals. There is no special pyloric chamber as in Protura or pyloric cuticular ring as in Collembola but a morphological transformation from midgut to hindgut cells. Eight globular Malpighian papillae, consisting of distal microvillated cells and flat proximal cells, open into the gut lumen via ducts formed by hindgut cells. The structure of the hindgut is complicated and can be divided into three segments. The anterior hindgut cells have an irregular shape and compact cytoplasm. A striking interdigitation between the large bottle-shaped epithelial cells and longitudinal muscle cells occurs in the middle segment of the hindgut. The thick cuticle gives rise to long spikes projecting into the gut lumen. The posterior hindgut cells possess the morphological features for water reabsorption. Some hypotheses are advanced about the function of the different regions of the gut.     

粉尘螨消化系统的形态学观察

光镜下观察了粉尘螨Dermatophagoides farinae消化系统结构,其组成包括：口前腔、前肠、中肠、后肠、肛门和唾液腺。口前腔由颚体围绕而成;前肠包括一个肌肉的咽和食道,食道从脑中穿过;中肠分为前中肠（包括一对盲肠）和后中肠,中肠的上皮细胞呈现多种形态; 后肠包括相对大的结肠和狭窄的直肠;消化腺为不规则形,位于脑前方。本文阐述了消化道的分支情况、显微结构及细胞形态。     

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丝状物质覆盖。后肠被有一层表皮。食道、中肠环中段、直肠细胞中含有微生物。【结论】本研究获得的合哑蝉消化道形态、组织结构和超微结构方面的信息为其功能分化研究提供了重要信息。同时,相关微生物的发现为进一步探讨共生菌与蝉总科昆虫的协同进化提供了信息。     

Sensory receptors associated with the stylets and cibarium of the rice brown planthopper,Nilapavarta lugens

Summary The stylets of Nilapavarta lugens consist of two maxillae that interlock to form separate food and salivary ducts partially surrounded by two mandibles. The ultrastructure of the sensory innervation of the stylets is described. Each maxilla possesses five neurones which extend to the tip of the stylet. The mandibles also contain five neurones, four of which are paired. The paired neurones comprise a shorter dendrite extending part of the way along the stylet and a longer one extending to the tip. The possible functions of these neurones are discussed. Gustatory receptors are located in the small passageway leading from the food duct to the cibarium. The receptors are in two distinct groups on the epipharyngeal side and one group on the hypopharyngeal side of the food canal. Two to five neurones innervate each receptor which connects to the food canal via a small pore.     

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.     

Characterization of the alimentary canal of the aphidophagous ladybird,Adalia bipunctata (Coleoptera: Coccinellidae): anatomical and histological approaches

The alimentary canal of the two‐spot ladybird Adalia bipunctata (Linnaeus) (Coleoptera: Coccinellidae) presents the foregut (stomodeum), the midgut (mesenteron) and the hindgut (proctodeum). The shortest region is the foregut and the longest is the midgut. The relative proportions of the main regions were found to be similar for males and females. In the foregut it was possible to distinguish the pharynx, the esophagus and the proventriculus but no crop. The hindgut is composed of the ileum, rectum and rectal canal. Generally the organ width is similar for males and females, but females presented a wider proventriculus. The epithelium of the foregut varied from squamous to simple cuboidal and columnar. In the midgut the epithelium is simple columnar with goblet and regenerative cells. The epithelium of the hindgut varied from simple cuboidal to squamous. Females presented thicker midgut epithelium whereas males presented thicker epithelium in the esophagus. The anatomy of the alimentary canal of A. bipunctata seems to conform to its carnivorous and recent phylogenetic status within the family Coccinellidae.     

Functional anatomy of the hypopharynx and the salivary pump in the feeding apparatus of the assassin bug Rhodnius prolixus (Reduviidae, Heteroptera)

Focussing on the blood-feeding reduviid Rhodnius prolixus, we investigated the structure and function of the hypopharynx in (1) conducting the saliva towards the mouthparts and (2) bringing together the salivary pump and the stylets to ensure the difficult task of supplying the two closed antidromic streams of blood and saliva, while allowing the mouthparts to be moved forth and back during the feeding process. The distal apex of the hypopharynx forms a needle-like structure that is X-shaped in cross section. It arranges the interlocking of the maxillae in a manner resembling the fixed slider of a zip-lock. Further proximal, the hypopharynx extends into the maxillary food channel as a wide tongue. The salivary pump possesses two separate efferent ducts. The dorsal duct originates in the retrograde angle of the cupula (part of the salivarium) and conducts saliva directly into the maxillary salivary channel. The ventral duct originates at the distal opening of the cupula. It extends into a bag, the distal opening of which can be closed by a ventral bolster-like cuticle and opened by muscles. We show for the first time for heteropteran mouthparts that the saliva is not exclusively discharged into the maxillary salivary channel (via the dorsal efferent duct of the salivary pump), but that a large amount of saliva directly flows into the tube of the labium (via the ventral efferent duct of the salivary pump), which encloses the piercing stylets. However, within a short section, saliva may also pass from the ventral salivary duct into the maxillary salivary channel. Similar double salivary efferent ducts are present in the reduviids Triatoma dimidiata, T. infestans, Dipetalogaster maxima, Panstrongylus megistus, in the pyrrhocorid Pyrrhocoris apterus, and in the pentatomid Troilus luridus. It might thus be a more common feature of the Heteroptera.     

Light and electron microscopy studies of the midgut and salivary glands of second and third instars of the horse stomach bot,Gasterophilus intestinalis

A morphological study of the midgut and salivary glands of second and third instars of Gasterophilus intestinalis (De Geer) (Diptera: Oestridae) was conducted by light, scanning and transmission electron microscopy. The midgut is anteriorly delimited by a proventriculus, without caeca, and is composed of posterior foregut and anterior midgut tissue from which a double‐layered peritrophic matrix is produced. The midgut can be divided into anterior, median and posterior regions on the basis of the structural and physiological variations of the columnar cells which occur along its length. Two other types of cell were identified: regenerative cells scattered throughout the columnar cells, and, more rarely, endocrine cells of two structural types (closed and open). Different secretion mechanisms (merocrine, apocrine and microapocrine) occur along the midgut epithelium. Abundant microorganisms are observed in the endoperitrophic space of the anterior midgut. The origin and nature of these microorganisms remain unknown. No structural differences are observed between the second and third instar midguts. The salivary glands of G. intestinalis second and third instars consist of a pair of elongated tubular structures connected to efferent ducts which unite to form a single deferent duct linked dorsally to the pharynx. Several intermediate cells, without cuticle, make the junction with the salivary gland epithelium layer. Cytological characteristics of the gland epithelial cells demonstrate high cellular activity and some structural variations are noticed between the two larval stages.     

Fine structure and function of the prosomal glands of the two-spotted spider mite,Tetranychus urticae (Acari,Tetranychidae)

Summary The prosomal glands of Tetranychus urticae (Acari, Tetranychidae) were examined light and electron microscopically. Five paired and one unpaired gland are found both in females and males. The silk spinning apparatus consists of paired silk glands which extend laterally on both sides of the esophagus into the pedipalps. There, they enter the terminal silk gland bag which opens into a silk bristle at the apex of the pedipalps. The salivary secretions are formed in three paired glands which have an interconnecting duct, the podocephalic canal. The dorsal podocephalic glands may produce a serous secretion, the anterior podocephalic glands a mucous secretion, and the coxal organ may add a liquid, ion-rich secretion. These secretions pass the podocephalic canal and reach the mouth at the apex of the gnathosome. The function of the paired tracheal organs and the unpaired tracheal gland is still unclear. The tracheal gland may produce a secretion which facilitates the movement of the fused chelicerae and the stylets.This study was financed by a grant from the Deutsche Forschungsgemeinschaft (DFG Se 162/12)     

The alimentary canal of <Emphasis Type="Italic">Blomia tropicalis</Emphasis> (Acari: Astigmata: Echymopodidae): the application of three-dimensional reconstruction technology

The domestic mite species Blomia tropicalis is an important indoor allergen source related to asthma and other allergic diseases in tropical and subtropical regions. Here, we describe the alimentary canal of B. tropicalis with the particular application of three-dimensional reconstruction technology. The alimentary canal of B. tropicalis resembles the typical acarid form consisting of the cuticle-lined foregut and hindgut separated by a cuticle-free midgut. The foregut is divided into a muscular pharynx and an esophagus. The midgut is composed of a central ventriculus, two lateral caeca, a globular colon and a postcolon with two tubiform postcolonic diverticula. The most common cells forming the epithelium of ventriculus and caeca are squamous and cuboidal. The globular cells contain a big central vacuole in the posterior region of the caeca. The epithelium of the colon and postcolon has significantly longer microvilli. The anal atrium is a simple tube with flattened epithelial cells. The spatial measurements of the three-dimensional model suggest that the paired caeca and central ventriculus occupy 55.1 and 34.6%, respectively, of the total volume of the alimentary canal and may play the key role in food digestion. J. Wu and F. Yang contributed equally.     

疥螨消化系统的显微和超微结构观察

疥螨消化系统由咽、食道、中肠、１对侧囊、结肠、直肠、肛门以及唾腺组成。应用透射电镜,可将中肠和侧囊壁上皮细胞分为鳞状细胞期、柱状细胞期、核变性圆细胞期和全变性细胞期等４种不同生理功能状态。可将唾腺细胞分为Ｉ期、Ⅱ期和Ⅲ期等３种不同生理功能时期。食道和中肠及侧囊内含物为絮状物。直肠前段肠壁具有较多微管。     

Gross morphology,histology, and ultrastructure of the alimentary system of Ricinulei (Arachnida) with emphasis on functional and phylogenetic implications

Ricinuleid functional mouthparts are the cucullus, the chelicerae, the pedipalps, and the labrum. These structures are movably jointed to the rest of the prosoma, most likely protruded upon hydrostatic hemolymph pressure and retracted by prosomal muscles. Seta‐like protrusions from the labrum and the pedipalpal coxae form a sieve‐like filter inside the preoral cavity and the mouth. Although the tip of the labrum can be elevated upon muscle constriction, ingestion of large, solid food particles is unlikely. The mouth has a crescent‐shaped cross section. The cuticle‐lined, also crescent‐shaped pharynx is equipped with a large dilator muscle but lacks antagonistic constrictor muscles. It represents a precerebral sucking pump. The triangular to Y‐shaped, cuticle‐lined esophagus is equipped with constrictor and dilator muscles. Its posterior part represents a postcerebral sucking pump. Four blind ending diverticula ramify from the anterior prosomal part of the entodermal midgut tube. Two of these diverticula remain inside the prosoma and form few short branches. The other two extend through the pedicel into the opisthosoma and ramify and coil there. A stercoral pocket protrudes ventrally out of the midgut tube. The most distal part of the midgut tube is modified into a contractile rectal gland. Its secretions may have defensive or physiological functions. A short anal atrium is formed by the cuticle‐lined ectodermal hindgut which opens at the end of the three‐segmented metasoma. The telescoping segments of the metasoma are protruded by hemolymph pressure and retracted by muscles. J. Morphol., 2011. © 2010 Wiley‐Liss, Inc.     

Ultrastructure of the digestive system of the Le fhopper Euscelidius variegatus Kirshbaum (Homoptera : Cicadellidae), with and without congenital bacterial infections

In the digestive system of Euscelidius variegatus Kirshbaum (Homoptera : (Cicadellidae), the close apposition of the anterior midgut with its posterior tabular midgut forms a filter chamber, which shunts excess water in the imbibed plant sap to the hindgut. Leafhoppers congenitally infected with a parasitic enteroform bacterium (designated BEV) had slightly atrophied digestive systems. There were numerous bacteria within the cells of the filter chamber, conical segment, and tubular midgut. Bacteria within the epithelium cells were usually enclosed within lysosomes. Epithelium cells swollen with large numbers of bacteria, had deteriorated cell membranes, and bacteria had erupted into the gut lumen. Leafhoppers not infected by BEV, harbored bacteria in the gut lumen, but not intracellularly within gut cells.     

The anatomy and histology of the midgut and hindgut of Charybdis (Goniohellenus) truncata (Fabricius, 1798) (Decapoda: Brachyura)

The midgut of C. (G.) truncata accounts for half of the postgastric intestinal tract. The paired anterior midgut caeca arise just behind the pyloric stomach, on either side of the midgut. The unpaired posterior midgut caecum arises dorsally at the rear end of the midgut, where this joins the hindgut. The midgut and its caeca help in the digestive absorption of food. The hindgut is of ectodermal origin and is lined with chitin of a collagenous nature. The connective tissue of the anterior part of the hindgut is packed with tegumental glands whose secretion contains both sulphated and weakly acidic mucosubstances, which facilitate the passage of faecal matter and help to bind food particles. The digestive gland - the hepatopancreas - opens into the anterior part of the midgut, below the anterior midgut caeca. Histologically, its tubules contain three different types of cells - "F", "R" and "B" cells.     

Functional morphology of the stomach of Corophium volutator Pallas

Corophium volutator Pallas is a small amphipod crustacean which burrows in inter-tidal mud on the British coast, and feeds on organic detritus, mainly vegetable, by selecting particles from the mud.
The alimentary canal consists of foregut, midgut and hindgut. The midgut is produced into a pair of anterior dorsal caeca, a pair of ventral caeca and a pair of posterior dorsal caeca.
The cardiac stomach has a large number of chitinous plates or ridges beset with hooks and spines for the trituration of food.
The pyloric stomach has long fine bristles which form an eifective filter apparatus and allow only fine particles of food to pass into the midgut, where they are digested and absorbed.
The hepato-pancreas secrete digestive enzymes and store reserve food material as oil globules.     

Salivary glands in Cicadidae (Hemiptera: Cicadoidea): comparative morphology, ultrastructure, and their phylogenetic significance

The present investigation provides information on gross morphology and ultrastructure of salivary glands of species in Cicadidae in detail. The structure of the salivary glands of 11 representative species from 10 genera belonging to three subfamilies of Cicadidae was studied using light microscopy and transmission electron microscopy. In the examined species, the salivary glands are paired structures, and each of which is comprised of a principal gland (pg) and an accessory gland (ag). The pg is divided into anterior and posterior lobes, and both of which consist of numerous long digitate lobules. The lobules at the base of the long digitate lobules of posterior lobe are greatly short; here, we named as “short lobules.” All the lobules vary in size, disposition, length, and shape. The anterior lobe and posterior lobes are connected by an anterior–posterior duct (apd). Two efferent salivary ducts (esd), derived from corresponding posterior lobes, fuse to form a short common duct which enters into the saliva syringe. The ag is composed of a greatly tortuous and folded accessory salivary tube, a gular gland (gg) constituting of several acini, and an accessory salivary duct (asd). The asd joins the esd at the place where the latter emergences. Constituents and arrangement of the salivary glands, the number and shape of the long digitate lobules in the anterior and posterior lobes, and the visibility of the apd were promising characters for the taxonomic and phylogenetic analysis of Cicadoidea. The variations of secretory granules in size, shape, and electron density in lobule cells of pg of Platypleura kaempferi probably indicating different materials are synthesized. The absence of the infoldings of basal plasma membrane in the basal area of the cells and the presence of electron-lucent vesicles in the cytoplasm of the gg cells of P. kaempferi might suggest that the secretions of gg are more watery.     

Digestive anatomy of Halella azteca (Crustacea,Amphipoda)

The digestive tract of the freshwater amphipod Hyalella azteca is a straight but differentiated tube consisting of foregut, midgut, and hindgut divisions. The foregut is subdivided into a tubular esophagus, a cardiac stomach, and a pyloric stomach. The cuticular lining of the cardiac stomach is elaborated into a set of food-crushing plates and ossicles, the gastric mill, while the pyloric cuticle forms a complex straining and pressing mechanism. Nine caeca arise from the midgut, seven anteriorly and two posteriorly. Four of the anterior caeca, the hepatopancreatic caeca, are believed to be the primary sites of digestion and absorption. The remaining caeca may be absorptive, secretory, or both. The much-folded hindgut wall is capable of great distention by extrinsic muscle action for water intake to aid in flushing fecal material out of the anus; such action also may stimulate antiperistalsis by intrinsic rectal muscles.