A morphological study on gills of the brown shrimp, Penaeus aztecus

The gills of Penaeus aztecus were examined by light and electron microscopy. They are dendrobranchiate, consisting of a central axis with biserially arranged branches that subdivide into bifurcating filaments. A septum divides the lumina of these structures into afferent and efferent channels. Hemolymph from the sternal sinus flows through the afferent channels into the filaments where it is directed into the efferent channels and finally to the pericardial cavity. In addition to these channels, numerous blood vessels permeate the gill. The cuticle covering the gill overlies a thin epithelium which is separated from hemolymph by a basal lamina. The epithelium, which is active in cuticle secretion, has a series of pillar processes that form subcuticular lacunae. The apical membranes of epithelial cells become folded in shrimp exposed to hypo- and hyperosmotic salinities. Granular cells that contain elaborate Golgi apparati and several types of granules are present throughout the gill. Nephrocytes resembling glomerular podocytes line the efferent channels. A large nerve traverses the septum in the axis.     

Structure of the Excretory System of Hawaiian Nerites (Gastropoda: Neritoidea)

Neritoidean gastropods are present in freshwater, brackish andmarine environments, which vary in salinity and exposure todehydration. In this study we examine the structure of the excretory systemof Hawaiian nerites, which indicates possible processes thatenable these gastropods to survive in a wide range of environmentsin the Hawaiian Islands. As is true of other nerites studied to date, the main excretorymechanism of Hawaiian nerites is through filtration of the bloodbetween podocytes in the auricle epicardium, resulting in productionof an ultra-filtrate, which collects in the pericardial cavity.No podocytes are present on the surface of the ventricle ofHawaiian nerites. The reno-pericardial canal conveys the urine tothe kidney, the epithelium of which is composed mainly of acidophiliccells in marine nerites. In brackish and fresh water species,baso-philic cells are present in addition to the acidophiliccells present in marine nerites. It is proposed that the basophilickidney cells allows non-marine nerites to osmoregulate and producea hyperosomotic urine at low salinities. A bladder is present,and empties into the mantle cavity near the gill by way of a ureter. (Received 26 November 1997; accepted 15 May 1998)     

The Ulrastructure of the Gill of the Lugworm Arenicola marina (L.) (Annelida,Polychaeta)

Arenicola marina gills are hollow, branched, body outgrowths with a central coelomic cavity and afferent and efferent vessels. The gill surface area per unit body weight is about 4 cm²/g wet weight. The blood vascular system anatomy differs from the tip to the base of the gill. In the distal branches of the gill the superficial afferent and efferent vessels are joined by connecting vessels. All vessels arise as spacings between the basal laminae of the thin epidermis and of the coelomic myoepithelium. The contractile part of this epithelium mainly borders the afferent and efferent vessels, whereas pedicel-like cytoplasmic processes extend from the cell bodies and mainly line the connecting vessels. In the proximal branches of the gill the afferent and efferent vessels located in the coelomic cavity are surrounded by the coelomic myoepithelium, and a peripheral blood plexus is present below the epidermis. The gill epidermis is everywhere thin and does not exhibit the characters of a transporting epithelium. The gill coelomic myoepithelium has several functions: (i) periodic contractions of the gill, propelling blood and coelomic fluid toward the central vascular and coelomic compartments; (ii) blood ultrafilration toward the coelomic cavity; (iii) probably transport, suggested by the specialized structures of the lateral membranes of the cells.     

Ultrastructure and histochemistry of the testicular efferent duct system and spermiogenesis in Opistognathus whitehurstii (Teleostei, Trachinoidei)

 Testis organization and spermatogenesis, with the emphasis on spermiogenesis, in Opistognathus whitehurstii are described by ultrastructural and histochemical methods. The germinal epithelium is extremely reduced and restricted to the periphery of the testis, while most of the organ is occupied by a highly developed system of testicular efferent ducts. A semicystic type of spermatogenesis is observed and in the germinal epithelium spermatogenesis occurs only until the spermatidal stage. Young spermatids are released into the lumen of the testicular lobules and mature to sperm within the efferent duct system. The epithelial cells of these ducts are involved in protein and glycogen secretion and in phagocytosis of degenerating germ cells and residual bodies cast off by developing spermatids. On the basis of these functions, the testicular efferent duct system cells are considered to be homologous to the Sertoli cells. A correlation between a highly developed testicular efferent duct system and semicystic spermatogenesis is examined and a possible functional meaning of this apparently unusual mode of sperm production is proposed. Accepted: 18 March 1997     

THE ANATOMICAL AND ULTRASTRUCTURAL BASIS OF PRIMARY URINE FORMATION IN BIVALVE MOLLUSCS

This paper examines the anatomical and ultrastructural basisof filtration in bivalves, and proposes a mechanism by whichthe filtrate is derived by a combination of hydrostatic pressureand suction generated by auricular and other muscles, assistedby cilia in the walls of the renopericardial canals. It is proposedthat the primitive auricular site of filtration becomes lessefficient with increasing size and may impair the contractilityof the auricle. The migration of the filter, including bloodsupply and muscles, to a separate pericardial site is indicatedby the discovery in two species, including Scrobicularia plana,with functional pericardial glands, of vestigial glands in theauricle. The development of a filtration site in the pericardialwall, where constraints on size do not exist, made possiblethe increase in the rate of urine formation which must accompanycolonization of estuarine and freshwater habitats. In freshwatergenera such as Anodonta the problem of creating a sufficientpressure gradient for a high rate of filtration is overcomeby the separation of that part of the pericardial cavity drainedby the renopericardial canal (the Nebenhöhle) from thechamber housing the heart. Contraction of predominantly transversemuscles in the wall of the Nebenhöhle is believed to beresponsible for expelling urine from it along the renopericardialcanals to the kidneys. The fine structure of the filtrationsite in ten species of bivalve is described. (Received 1 November 1992; accepted 6 December 1992)     

The venous system of the terrestrial crab Ocypode cordimanus (Desmarest 1825) with particular reference to the vasculature of the lungs

The respiratory system of Ocypode cordimanus consists of seven pairs of gills, modified for aerial gas exchange, and a single pair of lungs. Each lung is formed from the inner surface of the branchiostegite and the thoracic wall of the branchial chamber. The branchiostegal surface is increased by a fleshy infolding, the branchiostegal shelf, whilst the surface area of the thoracic lung wall is enhanced by a large flaplike fold. The anatomy of the major sinus systems and the vascular supply to the lungs were investigated. Venous hemolymph is supplied to the lungs potentially from all the major body sinuses. The dorsal, ventral, hepatic, and infrabranchial sinuses are all connected anteriorly to the two eye sinuses which distribute hemolymph to the lungs. Each eye sinus gives off five branches to the branchiostegal lung surface and one to the thoracic lung wall. These afferent vessels are highly branched and interdigitate closely with efferent vessels. The two systems are connected by flat lacunae lying just beneath the respiratory epithelium and these are believed to be the site of gas exchange. The efferent vessels empty into two pulmonary veins on each side, one serving the branchiostegal lung wall and the other the thoracic wall. The two vessels on each side fuse before joining the pericardial cavity as a single trunk on each side.     

Podocytes in bivalve molluscs: Morphological evidence for ultrafiltration

Summary In representatives from a survey of three major taxa of bivalves the pericardial glands were found in two distinct positions. In protobranches (Acila castrensis) and filibranch bivalves (Glycymeris subobsoleta, Chlamys hastata, Pecten caurinus, Placopecten magellanicus, Mytilus edulis andMytilus californianus) the pericardial glands are located on the auricular surface. In heterodonts (Mercenaria mercenaria, Clinocardium nuttallii andMya arenaria) the pericardial glands are found in an anterodorsal position to the pericardial cavity.The sites of ultrafiltration are described. They consist of podocytes with basally extending pedicels forming an interdigitating network apposed to a basal lamina. Other characteristics of this ultrafiltration barrier described are anionic sites on the basal lamina and presence of substructural components within the ultrafiltration slits between pedicels.The pathway for the ultrafiltrate in protobranchs and filibranchs is from the hemocoel through the basal lamina, through the ultrafiltration slits of the pedicel network, into the urinary spaces between the podocyte cell bodies and into the pericardial cavity. The pathway for the ultrafiltrate in heterodonts is from the hemocoel through the basal lamina, through the ultrafiltration slits of the pedicel network, into urinary spaces between the podocyte cell bodies, into the lumen of the pericardial gland tubules and into the pericardial cavity.All podocyte cells have electron dense granules, Golgi apparatus and vacuoles associated with their cytoplasm. Heterodont species have microvilli on the cell surfaces of the podocytes apposed to urinary spaces.In all cases the morphological sites of ultrafiltration were associated with the pericardial glands of the heart-pericardial complex.     

New aspects of the possible sites of ultrafiltration in annelids (oligochaeta)

Electron microscopic investigations of blood vessels were conducted to show sites of filtration such as podocytes or fenestrated endothelia. The endothelia of the blood vessels of Aelosoma hemprichi, Nais elinguis, Dero obtusa and Enchytraeus buchholzi consist of myoendothelial cells, chloragocytes and podocytes. The podocytes form large archs over a considerable area of the vessels. On the lumen side of the vessel there are several columnar processes which split into numerous small pedicels. The gaps between the adjacent pedicles are bridged by slit membranes. The podocytes are restricted to the front part of the ventral vessel. They are presumed to form a filtration surface. Furthermore, some parts of the ventral vessel are formed by a fenestrated endothelium, mainly in Enchytraeus buchholzi. In the vascular system of E. buchholzi two separate filtration sites were found. Additionally to the filtration site between ventral vessel and coelomic cavity a second filtration site was found in the front part of the body between blood sinus and coelomic cavity. In such areas the basement membrane is the only continuous layer between the blood vessel and the coelomic cavity. Its thickness is in the range of 40 nm. Possible filtration sites in the form of podocytes and irregular fenestrations could be localized at the border between the blood compartment and the coelomic compartment. It can be presumed that the primary urine may be formed by ultrafiltration of blood.     

Internal fertilization in Eudrilid earthworms with the description of a new Pareudriline genus and species (Oligochaeta) from Ghana

The female systems of Eudrilid earthworms in which internal fertilization seems probable are reviewed and the advantage conferred on the earthworms with these specializations is discussed. A new genus and species of Pareudrilinae is described from Ghana. The genus is characterized mainly by the presence of two unpaired, mid-dorsal oesophageal glands, one in segment vii and the other in segment viii. In addition, the posterior region of the oesophagus is dilated and specialized in segments xiii–xv. A hitherto undescribed system of afferent and efferent ducts is reported joining the receptaculum seminis with the spermathecal atrium and with the oviduct and its function is examined.     

Secretory Structures and Localization of Alkaloids inConium maculatumL. (Apiaceae)

In this paper histochemical investigations of the secretorystructures ofConium maculatumL., are described that discriminatedbetween ducts and vittae. The localization of alkaloids in seedlings,vegetative organs, flowers, and in the mericarp (during itsdevelopment from ovary to full maturity), was achieved usingspecific histochemical tests.Copyright 1998 Annals of BotanyCompany Conium maculatumL.; poison hemlock; secretory structures; alkaloids; histochemistry.     

Fine Structure of Heart,Pericardium and Glomerular Vessel in Cephalodiscus gracilis M'Intosh, 1882 (Pterobranchia,Hemichordata)

Heart, pericardium and glomerular vessel of Cephalodiscus gracilis have been studied with the electron microscope. The lumen of the heart is lined by a basal lamina and an associated epithelium, composed of myoepithelial cells with well developed thin and thick myofilaments. The heart is located in the pericardial cavity, which is deliminated by the pericardium. The latter is composed of two flat layers of myoepithelia with fused basal laminae. The outer layer of the pericardium is the protocoelomic lining, and the inner layer is the ‘parietal’ pericardial epithelium. The myoepithelium forming the heart wall can be considered to represent the ‘visceral’ pericardial epithelium. The spacious glomerular vessel is lined by a basal lamina, on which typical podocytes rest. These cells indicate that ultrafiltration takes place through the wall of the glomerular vessel. The lumen of the vessel contains fine granular material (presumably precipitated blood proteins), fibrils with a faint cross striation, suggesting that they represent collagen, and stellate cells, which in part line the vessel. Since ultrafiltration requires hydrostatic pressure, it is inferred that the blood flow is from the dorsal region then through the heart and into the glomerular vessel.     

Vascular anatomy of the gills of the stingarees Urolophus mucosus and U. paucimaculatus (Urolophidae,Elasmobranchii)

The branchial vascular anatomy of Urolophus mucosus and U. paucimaculatus was studied by scanning electron microscopical examination of critical-point-dried tissue or of vascular corrosion casts. The vasculature could be divided into arterioarterial and arteriovenous pathways, which channel the flow of blood through the gills. The arterioarterial pathway consists of an afferent branchial artery which gives rise to afferent distributing arteries that run through the tissues of the interbranchial septum and supply the afferent filament arteries of several filaments. Afferent filament arteries open regularly into a corpus cavernosum in the core of the filament; unlike other elasmobranchs no septal corpora cavernosa are found. At the tip of the filament, channels of the corpus cavernosum connect to a channel which passes across the distal end of the filament from afferent to efferent side. This channel always connects to the afferent filament artery, and in many filaments it connects to the efferent filament artery as well. In addition, a vascular arcade connects all the afferent filament arteries along the entire length of each hemibranch. The filament corpus cavernosum supplies the secondary lamellae. The lamellae drain into efferent lamellar arterioles which in turn drain into the efferent filament artery and the efferent branchial artery. The vascular anatomy of the arteriovenous pathway is similar to that described in other elasmobranchs and consists of arteriovenous anastomoses, found only arising from efferent arterial circulation, and the venolymphatic system, which is composed of the central venous sinus and the companion vessels.     

Morphology and immunolocalization of aquaporins 1 and 9 in the agouti (Dasyprocta azarae) testis excurrent ducts

This study investigated the morphology and immunoexpression of aquaporins (AQPs) 1 and 9 in the rete testis, efferent ducts, epididymis, and vas deferens in the Azara’s agouti (Dasyprocta azarae). For this purpose, ten adult sexually mature animals were used in histologic and immunohistochemical analyses. The Azara’s agouti rete testis was labyrinthine and lined with simple cubic epithelium. Ciliated and non-ciliated cells were observed in the epithelium of the efferent ducts. The epididymal cellular population was composed of principal, basal, apical, clear, narrow, and halo cells. The epithelium lining of vas deferens was composed of the principal and basal cells. AQPs 1 and 9 were not expressed in the rete testis. Positive reaction to AQP1 was observed at the luminal border of non-ciliated cells of the efferent ducts, and in the peritubular stroma and blood vessels in the epididymis, and vas deferens. AQP9 was immunolocalized in the epithelial cells in the efferent ducts, epididymis and vas deferens. The morphology of Azara’s agouti testis excurrent ducts is similar to that reported for other rodents such as Cuniculus paca. The immunolocalization results of the AQPs suggest that the expression of AQPs is species-specific due to differences in localization and expression when compared to studies in other mammals species. The knowledge about the expression of AQPs in Azara’s agouti testis excurrent ducts is essential to support future reproductive studies on this animal, since previous studies show that AQPs may be biomarkers of male fertility and infertility.     

Consciousness and Reflex

An analogy is drawn between the functions of consciousness and the model of a reflex. Consciousness consists of an afferent part, which is the perception of the external world; a central part, which is thought; and an efferent part, which is a decision concerning an action and the transmission of a motor command. At the basis of higher mental functions lies the unification of reflexes into complexes; and within these complexes, key structures are differentiated that synthesize qualitatively disparate information. The centers of integration for the effectuation of the afferent and efferent functions of consciousness are located in the posterior and anterior sections of the brain, respectively. Predominantly afferent and efferent stages, with localized foci of interaction, may also be distinguished in thought. The communicative function of consciousness is realized primarily by centers in the left hemisphere. A discrepancy between the afferent and efferent functions of consciousness may underlie certain forms of mental pathology.     

The morphology and vasculature of the lungs and gills of the soldier crab,Mictyris longicarpus

The five gill pairs of Mictyris longicarpus have the lowest weight specific area reported for any crab. The cuticle of the gill lamellae is lined with epithelial cells which have structural features characteristic of iontransporting cells. Pillar cells are regularly distributed in the epithelium and serve to maintain separation of the two faces of the lamellae. The central hemolymph space is divided into two sheets by a fenestrated septum of connective tissue cells. The dorsal portion of the marginal canal of each lamella receives hemolymph from the afferent branchial vessel and distributes it to the lamella while the ventral portion of the canal collects hemolymph and returns it to the efferent branchial vessel. The lung is formed from the inner lining of the branchiostegite and an outgrowth of this, the epibranchial membrane. Surface area is increased by invagination of the lining which forms branching, blind-ending pores, giving the lung a spongy appearance. The cuticle lining the lung is thin and the underlyng epithelial cells are extremely attenuated, giving a total hemolymph/gas distance of 90–475 nm. Venous hemolymph is directed close to the gas exchange surface by specialised connective tissue cells and by thin strands of connective tissue which run parallel to the cuticle. Air sacs are anchored in position by paired pillar cells filled with microtubules. Afferent hemolymph is supplied from the eye sinus, dorsal sinus, and ventral sinus. Afferent vessels interdigitate closely with efferent vessels just beneath the respiratory membrane. The two systems are connected by a “perpendicular system” which ramifies between the airways and emerges to form a sinus beneath the carapace and then flows back between the air sacs to the efferent vessels. The afferent side of the perpendicular system is the major site of gas exchange. Efferent vessels return via large pulmonary veins to the pericardial cavity. P_aO₂ levels were high (95.5 Torr), indicating highly efficient gas exchange.     

Permeability of the podocytes of Lumbricus terrestris (Annelida, Oligochaeta) to different markers

 The distribution of different injected markers between blood vessels and the coelomic cavity of Lumbricus terrestris was investigated by light and electron microscopy in order to show the direction of filtration and the permeability of the basement membrane of podocytes. The present results revealed that ultrafiltration takes place across the ventral vessel as well as through the peri-intestinal blood sinus of the typhlosolis. Furthermore, the filtration processes seem to be restricted to the front part of the body. Fluorescein isothiocyanate (FITC) [molecular weight (MW) 389.4 Da], Procion yellow (MW 873 Da), FITC-labelled dextrans (MW 39 kDa) and gold particles up to a diameter of 10–12 nm passed the podocytes. Evans blue (MW 960.8 Da) could not permeate through the podocytes. The injected gold particles were found inside the extracellular channels of the podocyte, between the microvilli-like processes of the podocyte and on the coelomic side of the peritoneal epithelium. The appearance of gold particles in the previously described structures indicated that filtration takes place from the lumen of the ventral vessel to the coelomic cavity. Accepted: 21 October 1996     

DEVELOPMENT OF THE ACINOUS AND ACCESSORY SALIVARY GLANDS IN NUCELLA LAPILLUS: (NEOGASTROPODA: MURICOIDEA)

The acinous and accessory salivary glands in Nucella lapillusare derived from two distinctly separate sites; the acinoussalivary glands evaginate from the walls of the buccal cavity,whilst the accessory salivary glands arise as paired invaginationsof the epithelium of the ventral lip of the mouth. During thedevelopment of the oesophagus, the acinous salivary glands growposteriorly and come to lie behind the nerve ring, but are pulledanteriorly through it when the proboscis elongates during development.The ducts of the accessory salivary glands fuse to form a singleduct with paired tubular glands during proboscis formation.The secretory cells in both pairs of salivary glands differentiateprior to the crawlaway's emergence from the egg capsule. Theontogeny of the salivary glands in Nucella shows that the accessorysalivary glands cannot be homologdus with the acinous salivaryglands or venom apparatus of the Conoidea. (Received 13 September 1996; accepted 25 November 1996)     

Ultrastructure of the body cavities in Phylactolaemata (Bryozoa)

Only species belonging to the bryozoan subtaxon Phylactolaemata possess an epistome. To test whether there is a specific coelomic cavity inside the epistome, Fredericella sultana, Plumatella emarginata, and Lophopus crystallinus were studied on the ultrastructural level. In F. sultana and P. emarginata, the epistome contains a coelomic cavity. The cavity is confluent with the trunk coelom and lined by peritoneal and myoepithelial cells. The lophophore coelom extends into the tentacles and is connected to the trunk coelom by two weakly ciliated coelomic ducts on either side of the rectum. The lophophore coelom passes the epistome coelom on its anterior side. This region has traditionally been called the forked canal and hypothesized to represent the site of excretion. L. crystallinus lacks an epistome. It has a simple ciliated field where an epistome is situated in the other species. Underneath this field, the forked canal is situated. Compared with the other species, it is pronounced and exhibits a dense ciliation. Despite the occurrence of podocytes, which are prerequisites for a selected fluid transfer, there is no indication for an excretory function of the forked canal, especially as no excretory porus was found. J. Morphol. 2009. © 2008 Wiley‐Liss, Inc.     

The Vascular System of Parhyale hawaiensis (Amphipoda)

Abstract A detailed study of the structure of the heart and the general disposition of the efferent (arterial) vessels and afferent (venous) vessels is presented. The vascular system of P. hawaiensis is compared with that of other species of amphipods and the differences are pointed out. All the appendages except the pleopods receive their efferent vessels directly from the heart and not from the sternal sinus.     

Ultrastructure of the Resin Ducts of Mangifera indica L. (Anacardiaceae). 1. Differentiation and Senescence of the Shoot Ducts

A detailed electron microscope study has led to the conclusionthat the resin ducts of the shoot of Mangifera indica L. developlysigenously. This study has also established several characteristicswhich can serve as criteria for a clear distinction betweenschizogenous and lysigenous cavities. The main characteristicsof lysigenous cavities are: (1) The presence of disorganized cytoplasm in the duct cavity. (2) The presence of wall remains attached to the wall of livingepithelial cells facing the cavity. (3) The presence of specific intercellular spaces at the cellcorners facing the duct lumen. Duct development starts with the disintegration of a file ofcells forming an initial cavity. Later the cells lining thiscavity differentiate into cells secreting lipophilic compounds.As a result of growth and differentiation of the tissues aroundthe duct, its lumen becomes compressed and comes to resemblea branched narrow slit. Such a slit may wrongly be regardedas an initial stage of a schizogenous duct. Disintegration ofepithelial cells occurs throughout all stages of development.Neighbouring cells partly fill the space which is released bydisintegrating cells. At the end of the stage of secretion thecytoplasm of all epithelial cells darkens, preceding their disintegration.This darkening is a gradual process which begins in the vicinityof ribosomes. When all dark epithelial cells disintegrate thecavity widens and the neighbouring parenchyma cells substitutefor the secretory epithelium without undergoing any significantchange in their cytoplasm. Mangifera indica L., mango, resin ducts, ultrastructure