Siphons and siphonal grooves in the digestive systems of the Echinoidea (Echinodermata)

Here we use histological sections and, to a limited extent, scanning electron microscopy to ascertain whether siphons or siphonal grooves parallel the stomach of five sea urchin species representing five higher taxa in the Echinoidea. We find a siphonal groove in Centrostephanus coronatus of the Diadematidae and in Caenopedina diomedeae of the Pedinidae; we find a siphon in Tromikosoma panamense of the Echinothurioida and in Strongylocentrotus purpuratus of the Camarodonta; and we find a hemisiphon in Aspidodiadema hawaiiense of the Aspidodiadematidae (it is currently unsettled whether this last group belongs in the Pedinoida or the Diadematoida). Several recent accounts of echinoid gut anatomy have claimed that species in the Echinothurioida have a siphonal groove instead of a siphon and that species in the Diadematidae and Pedinidae have siphons instead of siphonal grooves. The present work shows that these claims are mistakes and confirms that Holland and Ghiselin (1970) correctly described the distribution of siphons and siphonal grooves in the Echinoidea.     

Structure of the digestive tract of the pluteus larva of Dendraster excentricus (Echinodermata: Echinoida)

Summary Histological and ultrastructural observations of the digestive tract of eight-armed plutei of Dendraster excentricus are reported. The esophagus is divided into two regions. The uppermost is a narrow tube comprised of ciliated cells that assist in transporting food to the more bulbous lower esophagus where food particles are formed into a bolus prior to entering the stomach. The esophagus is surrounded by a network of smooth muscle fibers that are predominantly oriented circumferentially in the upper esophagus, and longitudinally in the lower esophagus. The musculature of the upper esophagus produces peristaltic contractions, whereas contractions of the muscle of the lower esophagus open the cardiac sphincter and force food from the lower esophagus into the stomach. Axons are associated with the ciliated cells and the muscles of the upper esophagus. The cardiac sphincter consists of a ring of myoepithelium, with cross-striated myofibrils oriented around the bases of the cells. The gastric epithelium is comprised of two cell types. Type I cells, which predominate, absorb and store nutrients, and may be the source of secreted digestive enzymes. Type II cells apparently phagocytize and intracellularly digest whole algal cells. The intestine is comprised of relatively unspecialized cells and probably functions primarily as a conductive tube for the elimination of undigested materials.     

Functional anatomy of the valves in the ambulacral system of sea urchins (Echinodermata,Echinoida)

Summary The water vascular system of sea urchins is examined with special reference to the valves positioned between the radial vessel and the ampullae of the tube feet. The lips of the valve protrude into the ampulla. Thus the valve functions mainly like a check valve that allows the unidirectional flow of fluid towards the ampulla. Each ampulla-tube foot compartment acts as a semi-autonomous hydraulic system. The lumina of the ampulla and the tube foot are lined with myoepithelia except for the interconnecting channels that pierce the ambulacral plate. The contraction of the ampulla results in an increasing hydraulic pressure that protrudes the tube foot, provided that the valve is closed. The retraction of the tube foot results in a backflow of fluid independent of the condition of the valve. The lips of the valve are folds of the hydrocoel epithelium. The pore slit lies in the midline. The perradial faces of the lips are covered with the squamous epithelium of the lateral water vessel. The ampullar faces are specialized parts of the ampulla myoepithelium. Turgescent cells which form incompressible cushions take the place of the support cells. The valve myocytes run parallel to the pore slit and form processes that run along the base of the ampulla and the perradial channel up to the podial retractor muscle. The findings lead to the hypothesis of multiple control of the ampulla-tube foot system: (1) The mutual activity of the ampulla and the tube foot is indirectly controlled by the lateral and podial nerves which release transmitter substances that diffuse through the connective tissue up to the muscle layers. (2) A muscle-to-muscle conduction causes the simultaneous contraction of the ampulla or the podial retractor muscles. (3) The valve muscles are directly controlled by the processes of the valve myocytes which make contact with the podial retractor. In extreme conditions a backflow of hydrocoel fluid towards the radial water vessel occurs.     

Phylogeny and classification of the Asteroidea (Echinodermata)

Post-Palaeozoic asteroids share a large number of derived characters of the ambulacral column and the mouth frame, and constitute the crown group of the monophyletic group Asteroidea. This crown group is here called the Neoasteroidea (new subclass). The stem species of the crown group lived in the Permian or early Triassic and so the evolution of the asteroids parallels that of the echinoids. Character distribution within the Neoasteroidea, especially morphology of the skeleton, digestive system, larvae and tube feet, allows subdivision into four orders (Paxillosida, Notomyotida, Valvatida, Forcipulatida). The latter three orders possess the synapomorphy of suckered tube feet and are united as the Surculifera (new superorder); the Paxillosida are their primitive sister group. Palaeozoic asteroids represent the stem group of the class, and may be divided into plesions according to the order of appearance of synapomorphies with the crown group. Classification of Palaeozoic asteroids requires much further study. The appearance of new characters within the crown group asteroids, such as suckered tube feet, implies that these were absent in the stem group. The range of life-habits possible in Palaeozoic asteroids can thus be partly deduced from evidence provided by living asteroids. Palaeozoic asteroids are deduced to have lacked suckered tube feet and were presumably unable to evert the stomach; hence they were precluded from life on hard substrates and extraoral feeding on epifaunal organisms. It is suggested that they lived on soft substrates by deposit feeding, scavenging and predation on small benthos.     

Phylogeny of Early Cretaceous spatangoids (Echinodermata: Echinoidea) and taxonomic implications

A phylogenetic analysis of 36 species provides a test for the taxonomy and the history of Early Cretaceous spatangoids. Most taxonomic units from genera to suborders are consistent with the proposed phylogenetic framework. We retain Hemiasterina, Micrasterina, Hemiasteridae, Schizasteridae, Hemiaster , Heteraster , Mecaster , and Periaster as original monophyletic groups. However, all of these clades originate without the classical apomorphies normally ascribed to them. We suggest a revision of their diagnoses and of the generic attributions of basal species. Some ill-defined, 'primitive', and paraphyletic taxa are recognised: Toxaster , Epiaster , Palhemiaster , and Toxasteridae. Even if they do not have phylogenetic meaning, they are retained here, pending a more complete revision.     

Ultrastructural investigation of matrix-mediated biomineralization in echinoids (Echinodermata,Echinoida)

Summary The formation of echinoderm endoskeletons is studied using echinoid teeth as an example. Echinoid teeth grow rapidly. They consist of many calcareous elements each produced by syncytial odontoblasts. The calcification process in echinoderms needs (1) syncytial sclerocytes or odontoblasts, (2) a spacious vacuolar cavity within this syncytium, (3) an organic matrix coat in the cavity. As long as calcite is deposited, the matrix does not touch the interior face of the syncytium. The cooperation between syncytium, interior cavity and matrix coat during the mineralization process is discussed. The proposed hypothesis applies to the formation of larval skeletons, echinoderm ossicles and echinoid teeth.When calcite deposition ceases the syncytium largely splits up into filiform processes, and the skeleton is partly exposed to the extracellular space. However, the syncytium is able to reform a continuous sheath and an equivalent of the cavity and may renew calcite deposition.The tooth odontoblasts come from an apical cluster of proliferative cells, each possessing a cilium. The cilium is lost when the cell becomes a true odontoblast. This suggests that cilia are primitive features of echinoderm cells. The second step in calcification involves the odontoblasts giving rise to calcareous discs which unite the hitherto single tooth elements. During this process the odontoblasts immure themselves. The structures necessary for calcification are maintained until the end of the process.The mineralizing matrix is EDTA-soluble. The applied method preserves the matrix coating the calcite but more is probably incorporated into the mineral phase and dissolved with the calcite.Abbreviations A adhesive point (LNC) - B adaxial bag - bb basal body (ci) - CA calcareous deposits - cb cytoplasmic bladder (cp) - ce centriole - ci cilium - cp cable-like cell process - cv condensing vacuole - dp distal processes (sh) - E epithelium of the tooth - ex extracellular space - f extracellular fibrils - ga gasket (sh) - ic interior cavity - L lamellae (LNC) - LNC lamellae needle complex - m mitochondrium - mc matrix coat - MF main fold (P) - MI mitosis - mt microtubules - N nucleus - O odontoblast - P primary plate - Ph phagocyte - PR proliferative cell - pr prism - rb reserve body - RER rough endopl. reticulum - rl rootlet (ci) - RY relatively youngest plate - s satellite (bb, ce) - sh synplasmic sheath (O) - SP secondary plate - sv smooth-walled vesicle - TF transversal fold (P) - U umbo (P) - v Golgi vesicle - Y youngest tooth element     

Choanocyte-like cells in the digestive system of the starfish Marthasterias glacialis (Echinodermata)

Two types of choanocyte-like cells have been found in the digestive tract of the starfish. Type I choanocytes are in the lining epithelium of all organs of the digestive system. These are narrow, columnar cells strongly anchored basally and expanded apically into a protuberance projecting into the lumen. A prominent flagellum surrounded by microvilli projects from the center of this protuberance. Apical cytoplasm contains numerous mitochondria, secondary lysosomes, and multivesicular bodies. A distinctive characteristic of these cells is a filament bundle that traverses the length of the cell from its region of attachment on the rootlet of the flagellar basal body to its terminus on the basal plasma membrane. Between the attenuated basal ends of type I cells are the nerve fibers of an intraepithelial nerve plexus. Thickness of the plexus is correlated with the quantity of type I cells in the epithelium. Type II choanocytes are in the cuboidal coelomic epithelium that forms the outer layer of digestive tract organs. These cells are smaller than those of type I, and they have an apical collar surmounted by a ring of 13 microvilli. Within the collar is a cup-shaped depression with a central flagellum. Coated vesicles, secondary lysosomes, and phagocytic infoldings are observed in and near the collar cytoplasm. Filament bundles similar to those in type I choanocytes are also observed in coelomic epithelial cells that are sufficiently tall. Injection of peroxidase into the stomach and ferritin into the coelom results in phagocytic uptake of these macromolecules by type I and type II choanocytes, respectively.     

The movement of proteins across the insect and tick digestive system

The movement of intact proteins across the digestive system was shown in a number of different blood-feeding and non-blood-feeding insects in the orders Blattaria, Coleoptera, Diptera, Hemiptera, Lepidoptera, Orthoptera, Neuroptera and Siphonaptera, as well as in two tick families Ixodidae and Argasidae. Protein movement was observed for both normal dietary and xenobiotic proteins, which suggest that the mechanism for transfer is not substrate specific. The number of studies on the mechanism of movement is limited. The research so far suggests that movement can occur by either a transcellular or an intercellular pathway in the ventriculus with most of the research describing the former. Transfer is by continuous diffusion with no evidence of pinocytosis or vesicular transport common in mammalian systems. Proteins can move across the digestive system without modification of their primary or multimeric structure and with retention of their functional characteristics. Accumulation in the hemolymph is the result of the protein degradation rate in the gut and hemolymph and transfer rate across the digestive system and can be highly variable depending on species. Research on the development of delivery systems to enhance protein movement across the insect digestive system is in its infancy. The approaches so far considered with some success include the use of lipophilic-polyethylene glycol (PEG) polymers, the development of fusion proteins with lectins, reduced gut protease activity and the development of amphiphilic peptidic analogs. Additional research on understanding the basic mechanisms of protein delivery across the insect digestive system, the importance of structure activity in this transfer and the development of technology to improve movement across the gut could be highly significant to the future of protein and nucleic acid-based insecticide development as well as traditional chemical insecticidal technologies.     

Functional morphology of coronal and peristomeal podia in Sphaerechinus granularis (Echinodermata,Echinoida)

Summary Coronal podia of Sphaerechinus granularis are anchoring (adhering) appendages involved in either locomotion or capture of drift materials. Adhesion is not due to the presumed sucker action of the disc but relies entirely on secretions of the disc epidermis. Peristomeal podia function in wrapping together food particles or food fragments in an adhesive material thus facilitating their capture by the Aristotle's lantern. In both types of podia, the disc epidermis is made up of four cell types: non-ciliated secretory cells (NCS cells) that contain graules whose content is at least partly mucopolysaccharidic in nature, ciliated secretory cells (CS cells) containing granules of unknown nature, ciliated non-secretory cells (CNS cells) and support cells. The cilia of CS cells are subeuticular whereas those of CNS cells, although also short and rigid, traverse the cuticle and protrude in the outer medium. All these cells are presumably involved in an adhesive/de-adhesive process functioning as a duogland adhesive system. Adhesive secretion would be produced by NCS cells and de-adhesive secretion by CS cells. These secretions would be controlled through stimulations by the two types of ciliated cells (receptor cells) which presumably interact with the secretory cells by way of the nerve plexus. This model of adhesion/de-adhesion fits well with the activities of both coronal and peristomeal podia. The secretion of NCS cells would make up a bridge of adhesive material between a podium and the substratum (coronal podia) or would coat and gather food particles (peristomeal podia), respectively. The de-adhesive material enclosed in the granules of CS cells would allow the podia (either coronal or peristomeal) to easily become detached from the substratum and to always remain clear of any particles.Research Assistant, National Fund for Scientific Research (Belgium)     

Fine structure and presumed functions of the pedicellariae of Echinocardium cordatum (Echinodermata,Echinoida)

Summary Tridactylous, trifoliate, and globiferous pedicellariae occur on the body surface of Echinocardium cordatum. Tridactyles have three forms: the typical, the rostrate, and the large forms. Both typical and rostrate tridactyles and trifoliates occur all around the echinoid body (trifoliates are, however, 4 times more numerous than tridactyles). Large tridactylous and globiferous pedicellariae are restricted to the peribuccal area.As a general rule tridactyles and trifoliates are similar in morphology. The distal part of the valves forms an open blade and bears lateral teeth and/or denticles (single or in combs). The stalk consists of a rigid proximal part supported by an axial rod and a flexible distal part which includes an axial fluid-filled cavity. The cavity is surrounded by muscle fibers and acts as an hydroskeleton, allowing the undulating-coiling movements of the flexible part of the stalk. Trifoliates are always active while tridactyles react only to direct or indirect mechanical stimulation.The valves of the globiferous pedicellariae have a tubular distal part whose upper opening is surrounded by teeth. There is no differentiated venom gland but a cluster of epithelial glandular cells located at the level of the valve upper opening. A small ciliary pad occurs just below the glandular cluster. Globiferous stalks are not flexible, being supported for their full length by an axial rod. Globiferous pedicellariae appear to be sensitive only to chemical stimulation.The presumed functions of E. cordatum pedicellariae are (1) cleaning of the body surface and ciliary structures (trifoliates), (2) protection against sedimenting particles (tridactyles), and (3) defense of the peribuccal area against potential small predators (globiferous pedicellariae).     

The sphaeridia of sea urchins: ultrastructure and supposed function (Echinodermata,Echinoida)

Summary Sphaeridia are minute skeletal appendages of the echinoid test which are considered to be sense organs, organs of equilibrium, according to their shape. The sphaeridium forms a functional unit with the tubercle to which it adheres. The tubercle is encircled by a basiepithelial nerve ring of the epidermis. A circle of regularly arranged myocytes stretches from the tubercle to the sphaeridium. The muscles are distant from each other. The myofibrillar processes enter the pore space of the sphaeridial skeleton to which they are anchored by tendons; tendons are absent in the tubercle region. The cell bodies of the myocytes lie opposite to the nerve ring outside the skeleton. In this region the muscle cells and the nerve ring are in contact with each other, their basal laminae fuse. Tensions of the various myocytes are dependent on the position of the top-heavy sphaeridium. The nerve ring contains neurones which are provided with a cilium which lies close to the contact region with the myocytes. This arrangement leads to the assumption that the nerve cells in question have a proprioceptor function. Unique filter cells are present in the pore spaces of the sphaeridium and the tubercle. They possibly detoxicate the extracellular fluid that surrounds the myocytes. Phagocytes loaded with spacious phagosomes are crowded in the adjacent pore spaces. They are possibly extruded via the epidermis. Filter cells and phagocytes have obviously to do with the metabolism within the sphaeridium-tubercle-system.     

Ultrastructure and organization of the epineural canal and the nerve cord in sea urchins (Echinodermata,Echinoida)

Summary The radial nerve cord ofMespilia globulus has been examined as an example of echinoid nerve cords. In the radius of echinoids only the ectoneural component of the nerve cord is present which is a derivative of the ectoderm. The nerve cord runs in the interior of the body and is accompanied by the epineural canal. In echinoids, the neuroepithelium makes up the upper and side walls of the epineural canal. Each lateral branch of the nerve cord forms a sort of neural tube. It encloses a branch of the epineural canal which represents an open connection with the sea water. Thus, the epineural canal exhibits numerous openings which probably allow sea water to flow back and forth. This organization is unique in echinoderms. — The neuroepithelium exhibits the organization of an epidermis with well-developed nervous elements. Glial cells are not present. The support cells are the true epithelial cells. Their monociliated cell bodies border the lumen and, by means of cytoplasmic stems that contain a bundle of filaments, they reach up to the basal lamina. The nerve cells and their trunk of nerve fibres fill the spaces between the support cells. — Three types of nerve cells can be distinguished according to their polarity: (1) Primary sensory cells that project a cilium into the epineural canal, the axon hillock region is at the opposite pole. (2) Subluminal cells whose cilium originates in the axon hillock region. (3) Neurones that lie within the trunk of nerve fibres. They are highly stretched in the direction of the nerve cord and are also provided with a cilium. Types 2 and 3 may be homologized with the basal nerve cells of the epidermis. They are possibly multipolar. — The lateral nerve cords make contact with the ampulla and pass the ambulacral plate parallel to the channel that connects the ampulla and the tube foot. The activity of the tube foot-ampulla system is possibly controlled by means of transmitter substances that diffuse through the connective tissue layer between the nerve cord and the myoepithelia of the ampulla and the tube foot respectively.     

Four lines of spermatid development and dimorphic spermatozoa in the sea urchin Anthocidaris crassispina (Echinodermata, Echinoida)

 The process of sperm development in the sea urchin Anthocidaris crassispina was studied by light and electron microscopy. Similar to other echinoids studied, a single flagellum, striated rootlet and nuage-like materials were present in spermatogonia of A. crassispina. Spermatocytes near the diplotene stage showed intracellular localization of the axoneme which appeared to be a retracted flagellum prior to cell division. Fibrous filaments were associated with a proximal centriole in spermatocytes and spermatids and might be involved in movement of the proximal centriole. An acrosomal vesicle was developed and a residual body was formed in spermatids. The special development patterns in A. crassispina attributed to the presence of two patterns of tail development and two patterns of mitochondrial development during spermiogenesis. These four lines of spermiogenesis resulted in the formation of four morphological types of sperm cell, i.e. sperms with: (1) a symmetrical midpiece and posterior tail, (2) an asymmetrical midpiece and posterior tail, (3) a symmetrical midpiece and bent tail and (4) an asymmetrical midpiece and bent tail. Sperm cells with bent tails (type 3+4) were probably still at the late spermatid stage because results of scanning electron microscopy demonstrated gradual detachment and eventual straightening of the bent tail, and their percentage occurrence in the sperm population decreased significantly (P<0.05) towards the spawning season of A. crassispina. Spermatozoa with a symmetrical midpiece were dominant (averaging 70% occurrence in the sperm population) over those with an asymmetrical midpiece. The dimorphic spermatozoa in A. crassispina (types 1, 2) are both considered to be euspermatozoa as their morphology is typical for Echinoida. Accepted: 4 May 1998     

On the ultrastructure and the supposed function of the mineralizing matrix coat of sea urchins (Echinodermata,Echinoida)

Summary Echinoderm ossicles are part of the mesenchyme. Their formation and growth, with respect to the underlying tissues, is studied using echinoid spines and teeth and applying different methods of fixation. The calcification process in echinoderms is strictly intracellular and needs (1) syncytial sclerocytes which completely enclose (2) a vacuolar cavity which in turn contains (3) an organic matrix coat. Strictly speaking, each ossicle is nothing but the calcified vacuolar space of a single syncytium of sclerocytes. In fully grown parts, however, the continuous sheath may split open and the matrix-coated mineral may come into contact with the extracellular space. According to biochemical analyses the matrix consists of insoluble components, but most (95%) of its constituents are soluble in EDTA or weak acids. If routine transmission electron microscope methods are used the soluble components are lost and the matrix at best looks electron light. If tannic acid is added to the fixative the soluble matrix components are preserved and reveal further ultrastructural details of the biomineralization process in echinoderms. The matrix coat looks extremely electron dense. Further soluble material is to be found within the vacuolar space or attached to the vacuolar surface of the cytoplasmic sheath. The results lead to the opinion that the matrix coat consists of a hydrophobic framework of insoluble components that contains soluble components which guide the Ca through pores in the hydrophobic layers into the interior of the matrix-coated space. It is only within this space that the mineral is deposited.     

The digestive gland of the Southern Dumpling Squid (Euprymna tasmanica): structure and function

The cephalopod digestive gland plays an important role in the efficient assimilation of nutrients and therefore the fast growth of the animal. The histological and enzymatic structure of Euprymna tasmanica was studied and used in this experiment to determine the dynamics of the gland in response to feeding. The major roles of the digestive gland were secretion of digestive enzymes in spherical inclusions (boules) and excretion of metabolic wastes in brown body vacuoles. High levels of trypsin, chymotrypsin and α-amylase, low levels of α-glucosidase and negligible carboxypeptidase activity were produced by the gland. There was no evidence of secretion of digestive enzymes in other organs of the digestive tract. Within 60 min of a feeding event, the gland produced increasing numbers of boules to replace those lost from the stomach during the feeding event. Initially, small boules were seen in the digestive cells, they increased in size until they are released into the lumen of the gland where they are transported to the stomach. There was no evidence of an increase in activity of digestive enzymes following a feeding event, despite structural changes in the gland. However, there was large variation among individuals in the level of digestive enzyme activity. A negative correlation between boule and brown body vacuole density suggested that the large variation in enzyme activity may be due to the digestive gland alternating between enzyme production and excretion.     

The lantern of Aristotle: organization of its coelom and origin of its muscles (Echinodermata,Echinoida)

Summary Comparative ultrastructural analyses of the muscles that work the lantern of Aristotle support the opinion that the muscles in question are myoepithelially organized or derivatives of myoepithelia. They are part of the epithelium of the peripharyngeal cavity (=lantern coelom). The coelom epithelium may become multiplelayered in certain regions and is composed of (1) a layer of muscle cells that vary in number and size, (2) nerve cells and their processes that are interspersed between the muscle layer and (3) monociliated adluminal cells that build a continuous cell lining and completely cover the muscle layer. According to their complexity, the lantern muscles exhibit consecutive stages of myoepithelial variations and may finally simulate subepithelial musculature. The results of this study support the hypothesis of a histological development of subepithelial musculature from simple myoepithelia, although both epithelial and mesenchymal musculature may occur in the Echinodermata. Detailed knowledge of the organization of the lantern's coelom space was a prerequisite for the present study. In contrast to previous examinations the lantern coelom is not a continuous space, but is subdivided into several cavities that are partially completely separated from each other. On the one hand, this subdivision is probably caused by the sophisticated arrangement of the lantern's ossicles and on the other by the septa that give rise to muscles that fulfill different functions. lanter's ossicles and on the other by the septa that give     

The interpyramidal muscle of Aristotle's lantern: its myoepithelial structure and its growth (Echinodermata,Echinoida)

Summary The interpyramidal muscles of the lantern of Diadema setosum have been studied as an example of such muscles in regular echinoids. The light- and electron microscopic study proves that the interpyramidal muscle is nothing but a continuous, highly folded myoepithelium. Although it is a powerful and specialized comminator muscle its histological organization (a pseudostratified myoepithelium) is rather simple when compared with other echinoderm myoepithelia. It consists of only two cell types: 1) a single layer of well-developed myocytes and 2) monociliated adluminal cells that totally cover the myocytes and touch the basal lamina by thin basal processes. The interpyramidal muscle grows by addition of new folds to its upper region. Consecutive stages of the myoepithelial differentiation are found in each of the young folds. The origin of the cells which are necessarily added to the growing epithelium is unknown. The growth rate of the muscle is in accordance with the enlargement of the lantern ossicles. The respective data are discussed in detail.     

Occurrence of neurotensin-immunoreactive cells in the digestive tract of lower vertebrates and deuterostomian invertebrates

Summary In the mucosal epithelium of the digestive tract of two marine teleost bony fish, one cartilaginous fish, one cyclostome, and in that of two of three representatives of deuterostomian invertebrates studied, endocrine cells of open type were found, exhibiting immunoreactivity with antisera against C-terminal sequences of mammalian neurotensin and of the structurally closely related amphibian neurohormonal peptide xenopsin.From these observations, and from those of previous studies, it is suggested that neurotensin cells do not occur in the digestive tract mucosa until at the evolutionary level of the more highly developed deuterostomian invertebrates. Three evolutionary stages seem to exist in the distribution pattern. The first stage, characterized by few, widely scattered cells, is found in the uro- and cephalochordates, the cyclostomes, the cartilaginous fish, and the stomachless bony fish. In the second stage, comprising the remaining submammalian classes, including more highly developed bony fish, the typical distribution pattern is that of numerous neurotensin immunoreactive cells in the antrum, pylorus, and duodenum. The final stage of neurotensin evolution is found in higher mammals and is characterized by a great density of neurotensin immunoreactive cells in the ileum.Dedicated to Prof. Dr. J. Staubesand on the occasion of this 60th birthday     

Mechanical properties of sea-urchin lantern muscles: a comparative investigation of intact muscle groups in Paracentrotus lividus (Lam.) and Stylocidaris affinis (Phil.) (Echinodermata, Echinoidea)

The jaw apparatus, or lantern, of sea-urchins contains five pairs of retractor and protractor muscles which are responsible for lantern displacement. Using intact retractor or protractor groups, the force-length relations of these muscles were compared in two taxonomically distant species, Paracentrotus lividus and Stylocidaris affinis. The total contractile forces generated by the muscles can be resolved into vertical and horizontal components. It was found that the vertical component of the retractors is maximal at a lantern position which is significantly lower (i.e. more protruded) in Paracentrotus than in Stylocidaris. Total forces generated by the retractors were in both species maximal at or above the lantern `resting positions'. In Paracentrotus alone, the total force-displacement curves tended to be bimodal. It is hypothesized that the retractors of Paracentrotus contain two populations of muscle fibres, one adapted for jaw opening and one for lantern retraction. No significant differences in the properties of the protractors of the two species could be identified. The lantern of Paracentrotus is more mobile than that of Stylocidaris and is able to exploit a wider range of food sources. This investigation has shown that the force-length relations of the lantern muscles match their differing working conditions. Accepted: 3 November 1997     

Ultrastructure and immunolocalization of digestive enzymes in the midgut of Podisus nigrispinus (Heteroptera: Pentatomidae)

The predatory stinkbug Podisus nigrispinus has been utilized in biological control programs. Its midgut is anatomically divided into anterior, middle and posterior regions, which play different roles in the digestive process. We describe the midgut ultrastructure and the secretion of digestive enzymes in the midgut of P. nigrispinus. Midguts were analyzed with transmission electron microscopy and the digestive enzymes amylase, cathepsin L, aminopeptidase and α-glucosidase were immunolocalized. The ultrastructural features of the digestive cells in the anterior, middle and posterior midgut regions suggest that they play a role in digestive enzyme synthesis, ion and nutrient absorption, storage and excretion. The digestive enzymes have different distribution along the midgut regions of the predator P. nigrispinus. Amylase, aminopeptidase and α-glucosidase occur in three midgut regions, whereas cathepsin L occurs in the middle and posterior midgut regions. The anterior midgut region of P. nigrispinus seems to play a role in water absorption, the middle midgut may be involved in nutrient absorption and the posterior midgut region is responsible for water transport to the midgut lumen.