Functional morphology of the locomotory podia ofHolothuria forskali (Echinodermata,Holothuroida)

Summary The ventral surface ofHolothuria forskali (Holothuroida, Aspidochirotida) is almost completely covered by small-sized podia that are locomotory. Each podium consists of a stem that allows the podium to lengthen, to flex, and to retract, and this is topped by a disc that allows the podium to adhere to the substratum during locomotion. Podia ofH. forskali do not end in a sucker and their adhesion to the substratum thus relies entirely on the disc epidermal secretions. The disc epidermis is made of five cell types: non-ciliated secretory cells of two different types that contain granules whose content is either mucopolysaccharidic (NCS1 cells) or mucopolysaccharidic and proteinic in nature (NCS2 cells), ciliated secretory cells containing small granules of unknown nature (CS cells), cilitated nonsecretory cells (CNS cells), and support cells. The cilia ofCS cells are subcuticular whereas those ofCNS cells, although also short and rigid, traverse the cuticle and protrude in the outer medium. During locomotion, epidermal cells of the podial disc are presumably involved in an adhesive/de-adhesive process functioning as a duogland adhesive system. Adhesive secretions would be produced byNCS1 andNCS2 cells and de-adhesive secretion byCS cells. All these secretions would be controlled by stimulations of the two types of ciliated cells (receptor cells) which presumably interact with the secretory cells by way of the nerve plexus. The lack of suckers and the coexistence of two adhesive cell types in the disc epidermis give the locomotory podia ofH. forskali a compromise structure which would perhaps explain their ability to move as efficiently along soft and hard substrata.     

The venom apparatus of the globiferous pedicellariae of the toxopneustid Sphaerechinus granularis (Echinodermata,Echinoida): Fine structure and mechanism of venom discharge

Summary Globiferous pedicellariae of Sphaerechinus granularis are venomous defensive appendages consisting of a stalk bearing a head made of three movable jaws. Each jaw is supported by a calcareous valve ending with a terminal grooved tooth. A venom apparatus is located in each jaw and consists of a venom gland surrounded by a muscular envelope and terminating in a duct which completely encircles the terminal tooth of the valve. Contrary to previous statements, the duct does not lie inside the groove of the terminal tooth. In mature pedicellariae, the venom is stored in intracellular vacuoles of highly differentiated cells which are no longer active. The cells fill the whole space of the venom gland which is without a lumen; they are segregated into two types that occur in distinct regions and differ from each other by morphological and staining properties of their secretions. Upon contraction of the muscular envelope, the venom is released via a holocrine mechanism and infiltrates the predator's tissues through the wound inflicted by the three calcareous teeth of the valves. In no case is the venom emitted through the tooth groove.     

Functional morphology of regular echinoid tests (Echinodermata,Echinoida): a finite element study

Functional morphology of the calcareous test ofEchinus esculentus was investigated by parametric finite element analysis, an engineering technique developed for numerical analysis of the behaviour of complex structures responding to external forces. Finite element models of the test were generated by methods of Computer Aided Geometric Design (CAGD) to calculate the mechanical responses to different types of loading. The load cases included vertical, concentrated load at the apex, vertical, distributed load on the upper third of the test, internal pressure and tensile forces as introduced into the test by tube feet activity. The objectives were the shape of the test, the distribution of material and the alternating zones of porous and non-porous plates within the test.—Echinoid tests resist external loading without showing any specific points of failure. The thickened margins of the periproct and peristome apertures account for load-bearing capacity as well as the thickned meridional structures which carry a greater portion of stress than the thinner parts of the test. Distribution of material is not a response to concentrated loads on the apex nor to self-weight. Taken strictly, echinoid tests are not thin (or membrane) shells. Under loading, bending moments occur which influence the stress state in the entire test. The pneu hypothesis could not be confirmed. Adaptation of the test shape or of the distribution of material as a response to internal pressure does not exist. Tests of regular echinoids are especially well adapted to the mechanical activity of the ambulacral tube feet, i.e. the shape of the test, its flattening towards the substrate, the outward bulge of the ambulacra and the differential distribution of material within the test.     

Fine structure of the axial complex of Sphaerechinus granularis (Lam.) (Echinodermata: Echinoidea)

Summary Three regions of the axial complex in Sphaerechinus granularis can be distinguished: 1) The axial organ which protrudes from one side of the axial sinus; the sinus septum which separates the sinus from the body cavity and encloses the stone canal; the pulsating vessel which runs along the inside of the axial organ. 2) The blindly-ending terminal sinus in which the pulsating vessel broadens out to the contractile terminal process. 3) The ampulla of the stone canal which connects the axocoel and water vascular system and which opens out through the madreporite.A single-layered, monociliated coelomic epithelium surrounds all regions of the axial complex. This epithelium contains smooth muscle cells at the contractile areas. Canaliculi, surrounded by basal lamina, are formed through infolding of epithelia; they end blindly in the fluid and connective tissue -matrix of the inner structures.The lacunae of the dorso-ventral mesentery connect the periesophageal and the perianal haemal ring with the axial organ. The axial organ contains many coelomocytes rich in pigment and granules. These coelomocytes are separated into compartments by elastic fibres. Phagocytosis of whole cells and transformational stages of coelomocytes suggest storage and degradation functions. An excretory function via the water vascular system is also suggested.     

Integumentary resorption and collagen synthesis during regression of headless pedicellariae in Sphaerechinus granularis (Echinodermata: Echinoidea)

Ultrastructure of the resorption of integumentary tissues (ligaments, muscles, fibrous tissue, nerves, and skeleton) and the synthesis of collagen is described for the first time in echinoderms. Resorption is cell-mediated. Phagocytic cells are characterized by Golgi-derived putative primary lysosomes. Numerous secondary lysosomes and residual bodies occur in the bodies and processes of phagocytic cells. They engulf whole muscle cells and nerve fibres, as well as collagen fibril segments that exceed 1.5 m in length. Skeletoclastic cells resemble vertebrate osteoclasts, showing a ruffled border, lysosomes, and numerous mitochondria. They surround trabeculae with thick processes to delimit a tubular resorption site. Collagen synthesis occurs in the space formerly occupied by resorbed tissues. Synthesis is performed by fibroblastic cells containing organelles typical of vertebrate fibroblasts, namely distended cisternae of rough endoplasmic reticulum, Golgi cisternae with distended edges, and procollagen granules. Procollagen granules are apparently exocytosed directly to the extracellular matrix. Evidence indicates that resorbing (phagocytic and skeletoclastic) cells and fibroblastic cells may belong to a common phagocyte lineage. These cells share the ability to form elaborate processes and to become syncytial, and their nuclei exhibit iron-containing crystals.This project was supported by Contract 2.4527.89 from the Fonds de la Recherche Fondamentale Collective (Belgium). P.D. is a Research Associate of the National Fund for Scientific Research (Belgium). Contribution of the Centre Interuniversitaire de Biologie Marine.     

Functional morphology of the tentacles and tentilla of Coeloplana bannworthi (Ctenophora, Platyctenida), an ectosymbiont of Diadema setosum (Echinodermata, Echinoida)

 The tentacular apparatus of Coeloplana bannworthi consists of a pair of tentacles which bear, on their ventral side, numerous tentilla. Each tentacle extends from and retracts into a tentacular sheath. Tentacles and tentilla are made up of an axial core covered by an epidermis. The epidermis includes six cell types: covering cells, two types of gland cells (mucous cells and granular gland cells), two types of sensory cells (ciliated cells and hoplocytes), and collocytes, this last cell type being exclusively found in the tentilla. The core is made up of a fibrillar matrix, the mesoglea, which is crossed by nerve processes and two kinds of smooth muscle cells. Regular muscle cells are present in both the tentacles and tentilla while giant muscle cells occur exclusively in the tentilla. The retraction of the tentacular apparatus is an active phenomenon due to the contraction of both types of muscle cells. The extension is a passive phenomenon that occurs when the muscle cells relax. Tentacles and tentilla first extend slightly due to the rebound elasticity of the mesogleal fibers and then drag forces exerted by the water column enable the tentacular apparatus to lengthen totally. Once the tentacles and tentilla are extended, gland cells, sensory cells, and collocytes are exposed to the water column. Any swimming planktonic organism may stimulate the sensory cilia which initiates tentillum movements. Pegs of hoplocytes can then more easily contact the prey which results in a slight elevation of the nearby collocytes, the last being responsible for gluing the prey to the tentilla. Accepted: 1 April 1997     

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.     

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     

Macrostructure and evolution of the digestive system in Echinoida (Echinodermata)

The structure of the digestive system in Echinoida has long been puzzling since comparative studies have suggested that a derived structure, the siphon, has apparently evolved twice independently. New observations on the digestive system in five species of Cidaroida, four species of the Diadematoida and three species of Echinothurioida are presented. The results show that the four diadematoid species have a siphon and the three species of Echinothurioida have a siphonal groove, contrary to previous assertions. These observations make the macrostructure of the echinoid digestive system fully consistent with more recent phylogenetic hypotheses based on molecular and general morphological data, and support the idea that a siphon has evolved only once, in the stem lineage of the Acroechinoidea.     

Skeleton resorption in echinoderms: Regression of pedicellarial stalks inSphaerechinus granularis (Echinoida)

Summary When a globiferous pedicellaria ofSphaerechinus granularis injects its venom, the head autotomizes whereas the stalk remains on the test and enters a regression process with concomitant resorption of its supporting ossicle (i.e. the rod). Scanning electron microscope investigations of the morphological changes undergone by the stereom of resorbing rods show that: (1) resorption proceeds both axially and laterally, and leads to a reduction of approximately 80% of the original length of the rod, (2) secondary growth of new stereom processes occurs concomitantly with resorption but never ensures even a partial regeneration of the rod, and (3) resorption and secondary growth stop before the rod is totally destroyed leaving a static stump that remains in place up to 190 days. Particular resorption figures result from either the axial or the lateral resorption of the rod shaft. These consist chiefly of terraced conical cupules, dense cylinders and concentric lamellae whose walls or edges are typically made of closely piled and/or aligned subprismatic crystallites. Whatever their location along the rod, these crystallites always organize strictly parallel to the rod axis. Whether the crystallites are mosaic blocks composing larger monocrystalline units or discrete monocrystals themselves is for the moment unclear. A growth model, which accounts for the observed resorption figures, is proposed for the shaft of pedicellarial rods. According to this model, the early growth of the shaft would produce elongated, interconnected trabeculae (initial trabeculae) made of densely piled and perfectly aligned crystallites. Thickening and coalescence of adjoining trabeculae would progressively occur by adjunction around the initial trabeculae of successive and concentric layers of similarly arranged crystallites. Coalescent trabeculae would then be cemented together in a perforate stereom layer by the final deposition of larger crystallite layers surrounding the whole shaft periphery. Growth of secondary stereom processes occurs both in the resorbing rod (here the newly formed processes are resorbed soon after they have been produced) and in rods where resorption has stopped. These are always irregular processes that localize near or on the actual sites of resorption. It is suggested these processes result from an uncontrolled activation of the skeleton-forming cells in areas where the concentration of calcium ions increases as a consequence of calcite resorption.     

Non-respiratory podia of clypeasteroids (Echinodermata,Echinoides): II. Diversity

Summary There are five major types of non-respiratory podia in the Order Clypeasteroida: accessory, barrel-tipped, food groove, large food groove, and buccal. The anatomy of each type is intimately related to its function in the feeding mechanism of clypeasteroids. Accessory podia are found aborally and orally in some species, only aborally and ambitally in others. Accessory podia are largely sensory and manipulatory, but can be locomotory in the small fibulariids and juvenile sand dollars. Barrel-tipped podia have expanded disk muscles and connective tissue, and are usually found in two sizes, large and small. In species that have them they are usually restricted to the oral surface. These podia collect food and pass it towards the food grooves in the manner of a bucket brigade. Food groove podia are found only in species with food grooves. These podia are small, with reduced tip musculature and expanded secretory tissue for coating food with mucus. They transport food down the food grooves to the mouth. Large food groove podia are simply large versions of ordinary food groove podia. They help move the clumped food into the mouth area towards the buccals, and are found only in the Clypeasteridae and some scutellines. Buccal podia lack tip musculature, but possess tip support fibres and a single type of small secretory cell. They are sensory, and capable of manipulating particles into the mouth. Buccals are present in all families except the Clypeasteridae. Juvenile Echinarachnius less than 3 mm in diameter have only respiratory, accessory and buccal podia. Food groove and barrel-tipped podia start to differentiate from the accessories as the juvenile approaches a diameter of 4 to 5 mm. Clypeasteroid podial diversity increases the efficiency of the food collecting mechanism. The anatomy and distribution of podia on the oral surface of scutellines supports the fact that this surface is the prime food collecting area in all true sand dollars. The podia (not miliary spines) are the major source of mucus used during the feeding process and are the primary feeding appendages.     

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.     

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).     

Functional morphology of vibratile urnae in the synaptid holothuroid Leptosynapta inhaerens (Echinodermata)

Summary Vibratile urnae of Leptosynapta inhaerens are organized in three longitudinal bands along the mesenteries. An individual of 10 cm length usually houses about 4500 urnae. These are minute (300 Gmm high), S-shaped and hollow peritoneal organs consisting of an intracoelomic projection of the body wall mesothelium supported by a thin connective tissue layer. The urnal cavity is strongly ciliated. Each urna harbours a clump of coelomocytes at the lower part of its aperture. The clump is attached to the urna through spot-like desmosomes occurring between its inner-most coelomocytes and apical urnal cells. Clumps and urnae form functional units. Urnal cilia produce steady water currents through urnal cavities and whirls along urnal bands. The particulate material conveyed by the coelomic fluid enters the urnal cavity and is either trapped by coelomocyte pseudopodia or agglutinated by a mucoid substance that covers the clump's outer surface. Depending on individuals, clearance of coelomic fluid occurs from 2 to 3 h after experimental injection of particulate material. The effectiveness of coelomic fluid clearance appears to be due to the particular organization and location of urnae, viz. in longitudinal bands along the mesenteries.     

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.