Functional morphology of the stone canal in the sea urchin Eucidaris (Echinodermata: Echinoidea)

The lack of mesocoelomic pores and the existence of a stone canal connecting proto-and mesocoel are characteristic peculiarities of echinoderms in contrast with the situation in other trimeric archicoelomates. The ultrastructure of the stone canal has been studied in order to understand its function in the strategically important position between two coelomic spaces with different functions. The epithelium of the Eucidaris (Echinoidea) stone canal is composed of three cell types: (1) ciliated cells, (2) cells with long basal processes containing myofilaments, and (3) granulated cells, which may represent secretory neurons. Nerve fibres of two types are common in the epithelium. We consider the stone canal to be a structure controlling fluid transport; its wall may exert peristaltic movements or tonic contractions and dilations which are under control of the nervous system. The ciliated cells additionally may have phagocytotic capacities. Similarities with the fine structure of the wall of the mesocoelomic pores in the pterobranch Cephalodiscus are discussed.     

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.     

Ultrastructure of tentacles in the sipunculid worm <Emphasis Type="Italic">Thysanocardia nigra</Emphasis> Ikeda, 1904 (Sipuncula)

The ultrastructure of the tentacles was studied in the sipunculid worm Thysanocardia nigra. Flexible digitate tentacles are arranged into the dorsal and ventral tentacular crowns at the anterior end of the introvert of Th. nigra. The tentacle bears oral, lateral, and aboral rows of cilia; on the oral side, there is a longitudinal groove. Each tentacle contains two oral tentacular canals and an aboral tentacular canal. The oral side of the tentacle is covered by a simple columnar epithelium, which contains large glandular cells that secrete their products onto the apical surface of the epithelium. The lateral and aboral epithelia are composed of cuboidal and flattened cells. The tentacular canals are lined with a flattened coelomic epithelium that consists of podocytes with their processes and multiciliated cells. The tentacular canals are continuous with the radial coelomic canals of the head and constitute the terminal parts of the tentacular coelom, which shows a highly complex morphology. Five tentacular nerves and circular and longitudinal muscle bands lie in the connective tissue of the tentacle wall. Similarities and differences in the tentacle morphology between Th. nigra and other sipunculan species are discussed.Original Russian Text Copyright © 2005 by Biologiya Morya, Maiorova, Adrianov.     

Brachiopod tentacles: Ultrastructure and functional significance of the connective tissue and myoepithelial cells in Terebratalia

Summary The fine structure of the tentacles of the articulate brachiopod Terebratalia transversa has been studied by light and electron microscopy. The epidermis consists of a simple epithelium that is ciliated in frontal and paired latero-frontal or latero-abfrontal longitudinal tracts. Bundles of unsheathed nerve fibers extend longitudinally between the bases of the frontal epidermal cells and appear to end on the connective tissue cylinder; no myoneural junctions were found. The acellular connective tissue cylinder in each tentacle is composed of orthogonal arrays of collagen fibrils embedded in an amorphous matrix. Baffles of parallel crimped collagen fibrils traverse the connective tissue cylinder in regions where it buckles during flexion of the tentacle.The tentacular peritoneum consists of four cell types: 1) common peritoneal cells that line the lateral walls of the coelomic canal, 2) striated and 3) smooth myoepithelial cells that extend along the frontal and abfrontal sides of the coelomic canal, and 4) squamous smooth myoepithelial cells that comprise the tentacular blood channel.Experimental manipulations of a tentacle indicate that its movements are effected by the interaction of the tentacular contractile apparatus and the resilience of the supportive connective tissue cylinder. The frontal contractile bundle is composed of a central group of striated fibers and two lateral groups of smooth fibers which function to flex the tentacle and to hold it down, respectively. The small abfrontal group of smooth myoepithelial cells effects the re-extension of the tentacle, in conjunction with the passive resiliency of the connective tissue cylinder and the concomitant relaxation of the frontal contractile bundle.The authors wish to express their appreciation to Professor Robert L. Fernald for his advice and encouragement throughout the course of this study. Some of the work was conducted at the Friday Harbor Laboratories of the University of Washington. The authors are indebted to the Director, Professor A.O.D. Willows, for use of the facilities. Part of this study was supported by NIH Developmental Biology Training Grant No. 5-T01-HD00266 and NSF grant BMS 7507689     

Integument of Kamptozoa Barentsia discreta Busk, 1886

The integument of the colonial species Barentsia discreta has been investigated in the present work. On its greater length the integument is presented by a monolayered unciliated epithelium covered by a layer of microvillar cuticle. The floor of the atrial cavity and the frontal surface of tentacles is lined by ciliated epidermis covered by a protocuticle. Sensitive and secretory cells are present in the epidermis.     

Fine Structure of the Hepatic Sacculations of Glossobalanus minutus (Enteropneusta,Hemichordata)

Abstract The hepatic region of Glossobalanus minutus is characterized by deep foldings of the dorsal side of the gut epithelium which affect the neighbouring tissues and structures: coelomic spaces, musculature and epidermis. The following cell types of the gut epithelium are described: vacuolated cells, undifferentiated cells, two types of mucous cells and two types of granular secretory cells. The nature and function of the different cell types are discussed. Data on the general ciliation and subepithelial nerve plexus of the gut epithelium are also given, with special mention of a possible neuroendocrine secretion towards the subjacent blood spaces. A well-developed blood sinus (gut sinus) lies between the gut and the visceral peritoneum. The ultrastructural features of the gut epithelium and its close association with the blood sinus point to an absorptive function. The coelomic cavity is reduced to a narrow space limited by two peritoneal sheets (visceral and parietal) of myoepithelial nature. Amoebocyte-like cells (coelomocytes) occur free in the coelomic fluid, and muscular, unicellular bridges are attached to both peritoneal walls across the coelomic space. The dorsal epidermis follows the gut foldings and is formed by flat, overlapping cells. The present observations are compared with previous histological, histochemical and ultrastructural data.     

Organogenesis in the budding process of the freshwater bryozoan Cristatella mucedo Cuvier, 1798 (bryozoa,phylactolaemata)

The phylogenetic position of bryozoans has been disputed for decades, and molecular phylogenetic analyzes have not unequivocally clarified their position within the Bilateria. As probably the most basal bryozoans, Phylactolaemata is the most promising taxon for large‐scale phylogenetic comparisons. These comparisons require extending the morphological and developmental data by investigating different phylactolaemate species to identify basal characters and resolve in‐group phylogeny. Accordingly, we analyzed the bud development and the organogenesis of the freshwater bryozoan Cristatella mucedo, with special focus on the formation of the digestive tract and differentiation of the coelomic compartments. Most parts of the digestive tract are formed as an outpocketing at the future anal side growing towards the mouth area. The ganglion is formed by an invagination between the anlagen of the mouth and anus. The lophophoral arms develop as paired lateral protrusions into the lumen of the bud and are temporarily connected by a median, thin bridge. All coelomic compartments are confluent during their development and also in the adult. The epistome coelom develops by fusion of two peritoneal infolds between the gut loop and overgrows the ganglion medially. The coelomic ring canal on the oral side develops by two lateral ingrowths and supplies the oral tentacles. On the forked canal, supplying the innermost row of tentacles above the epistome, a bladder‐shaped swelling, probably with excretory function, is present in some adults. It remains difficult to draw comparisons to other phyla because only few studies have dealt with budding of potentially related taxa in more detail. Nonetheless, our results show that comparative organogenesis can contribute to phylactolaemate systematics and, when more data are available, possibly to that of other bryozoan classes and bilaterian phyla. J. Morphol., 2011. © 2010 Wiley‐Liss, Inc.     

The Development of the Brachiopod Crania (Neocrania) anomala (O. F. Müller)and its Phylogenetic Significance

The freely spawned eggs of Crania go through radial cleavage, embolic gastrulation, and the posteroventral part of the archenteron forms mesoderm through modified enterocoely. The blastopore closes in the posterior end of the larva. The ciliated, lecithotrophic larva has four pairs of coelomic pouches and three pairs of dorsal setal bundles. At metamorphosis, the larva curls ventrally by contraction of a pair of midventral muscles, which are extensions of the first pair of coelomic sacs; the larva attaches by the epithelium just behind the closed blastopore. The brachial valve is secreted by the middle part of the dorsal epithelium and the pedicle valve is secreted by the attachment epithelium. The second pair of coelomic sacs develop small attachment areas at the edge of the dorsal valve and become the lophophore coelom (mesocoel); the third pair of coelomic sacs become the body coelom (metacoel) with the adductor muscles. The posterior position of the closing blastopore is characteristic of deuterostomes. The ventral curving of the settling larva and the formation of both valves from dorsal epithelial areas indicate that the brachiopods have a very short ventral side as opposed to the phoronids. It is concluded that both groups have originated from a creeping ancestor with a straight gut.     

The basiepithelial nerve plexus of the viscera and coelom of eleutherozoan echinodermata

Summary The organisation of the basiepithelial nerve plexus in the alimentary canal of a starfish and the water vascular system of a sea-urchin is described. The plexus contains varicose aminergic neurones which terminate adjacent to the ciliated epithelial cells. It is proposed that the basiepithelial plexus innervates these cells and controls ciliary beating. The distribution of the basiepithelial plexus in various tissues described by other workers is dicscussed particularly in relation to whether it is the coelomic epithelium or the luminal epithelium which is innervated. It is concluded that where there is both an endothelium and a coelomic epithelium only one is innervated. The muscles, where present, of the viscera are innervated by a separate nervous system. The muscles are always on the opposite side of the non-cellular connective tissue sheath to the basiepithelial plexus.     

Ultrastructural Studies of the Visceral Muscles of Chaetognaths

The visceral musculature of Chaetognaths was studied with special attention given to the digestive apparatus muscle. In the head the digestive apparatus muscle is relatively thick; individual muscles are difficult to distinguish at the anatomical level; in the anterior part of the oesophagus discontinuous bundles and layers of cross-striated fibers are found. As a group however, the oesophageal musculature completely covers the oesophageal epithelium. The prominent muscle layers around the oesophagus probably help to force food into the intestine against the turgor pressure of the trunk cavity which tends to collapse the intestine. Around the intestine the musculature is largely circular and smooth. The intestinal epithelium is ciliated despite its muscular covering. Muscle fibers are not individually innervated. They form myoepithelial structures with various intercellular junction types. In the intestinal muscle the fibers show myoendothelial-like junctions. Sphincters composed of myoepidermal cells surround the anus and the female gonopores. The somatic side of the general cavity is lined with a polymorphic squamous epithelium. Sometimes myoepithelial cells are found, with the occasional presence of extracellular matrix basal to the layer of the squamous epithelium. The ontogenetic relations between the polymorphic epithelium and the composite ‘mesenteries’ remain to be established. We have now some idea about the architecture of the body of Chaetognaths in relation to contractile structures.     

Ultrastructure of the Blood System in the Phoronid Phoronopsis harmeri Pixell, 1912: 1. Capillaries

Four types of blood capillaries of the phoronid Phoronopsis harmeri are described. These are capillaries of the tentacles, of the body, of the stomach plexus, and of the vasoperitoneal tissue. The wall of capillary consists of cells of the coelomic lining, a layer of extracellular matrix, and separate endothelial cells. Myoepithelial coelomic cells of tentacle capillaries contain cross-striated fibers. In capillaries of the body and the stomach plexus, the myofilaments are smooth. In the cells of the wall of vasoperitoneal tissue capillaries, myofilaments are lacking. The cells of the vessel wall of the tentacles, the body, and the vasoperitoneal tissue bear a single cilium. The cells of capillaries of the stomach plexus lack a cilium. The ultrastructure of erythrocytes and amebocytes is described. In the cytoplasm of erythrocytes, there is a basal body. It is assumed that erythrocytes originated from the ciliary cells of the wall of the blood vessels.     

Ultrastructure and formation of the body cavity lining in Phoronis muelleri (Phoronida, Lophophorata)

Among other characteristics a trimeric coelomic compartmentation consisting of an anterior protocoel, followed by a mesocoel and a posterior metacoel is traditionally believed to substantiate the sister-group relationship between Lophophorata and Deuterostomia, together forming the Radialia. As molecular data cannot support this hypothesis a reanalysis of the coelomic cavities in Phoronida is undertaken, because corresponding coelomic compartmentation is widely accepted to support the Radialia hypothesis. A coelomic cavity can be recognized on the ultrastructural level because its lining is a true epithelium with polarized cells interconnected by apical adherens junctions. This study reveals that neither in larval nor adult Phoronis muelleri (Phoronida) an anterior cavity with such a lining is present. What on the light microscopic level leads to the impression of a cavity inside the larval episphere, actually is an enlarged subepidermal extracellular matrix with an amorphous, presumably gel-like filling, into which several muscle cells are embedded. Larvae, thus, possess only one coelomic cavity, the large trunk coelom of the larva which is adopted in the adult organization. The second coelomic cavity of adult P. muelleri, the lophophore coelom, develops as a double-layer of epithelialized mesodermal cells at the base of the adult tentacle buds and becomes fluid filled during metamorphosis. Like the larval episphere, larval tentacles and most parts of the blastocoel are filled by an amorphous matrix. Reanalysis of the literature and comparison with Brachiopoda and Bryozoa allows the hypothesis that a protocoel is lacking in all Lophophorata, and that merely two unpaired coelomic cavities, one tentacle and one trunk coelom, can be assumed for the ground pattern of this taxon. These results do not provide further evidence for the Radialia hypothesis, but also do not contradict it. Accepted: 28 August 2000     

Fine Structure of the Tentacles of Phoronis australis Haswell (Phoronida,Lophophorata)

The epidermis of the tentacles of Phoronis australis consists of six cell types: supporting cells, choanocyte-like sensory cells, both types monociliated, secretory A-cells with a mucous secretion, and three kinds of B-cells with mucoprotein secretions. On cross-sections of the tentacle, one can distinguish four faces: the frontal one, heavily ciliated and located between the two frontolateral rows of sensory cells, the lateral and the abfrontal ones. The orientation of the basal structures of the cilia is related to the direction of their beat. The basiepidermal nervous system is grouped mainly at the frontal and abfrontal faces. The basement membrane is thickest on the frontal face and consists of circular collagen fibrils near the epidermis and longitudinal ones near the peritoneum. All peritoneal cells surrounding the mesocoel are provided with smooth longitudinal myofibrils, and isolated axons are situated between these cells and the basement membrane. The wall of the single blood capillary in each tentacle consists of epitheliomuscular cells with circular myofilaments, lying on a thin internal basal lamina; there is no endothelium.     

Muscle development in squid: Ultrastructural differentiation of a specialized muscle fiber type

The ultrastructural differentiation of two muscle fiber types of the squid Sepioteuthis lessoniana was correlated with development of prey-capture behavior. Transmission electron microscopy was used to document the differentiation of the fast-contracting cross-striated muscle cells of the tentacles and the obliquely striated muscle cells of the arms of specimens sampled at one week intervals from hatching to 5 weeks. By using high-speed video recordings, the ultrastructural differentiation was correlated with changes in prey-capture behavior that occur during development and growth. The ultrastructural analysis focused on the muscle cells of the transverse muscle of the tentacles and the transverse muscle of the arms. For the first 2 weeks after hatching, the tentacle transverse muscle fibers do not show the adult ultrastructure and are indistinguishable from the obliquely striated fibers of the transverse muscle of the arms. Transverse striation of the tentacle muscle cells appears at approximately three weeks and adult ultrastructure is present by 4–5 weeks after hatching. The high-speed video recordings show correlated behavioral changes. During the first 2–3 weeks after hatching, the animals use a different prey-capture mode from the adults; they jet forward and capture the prey with splayed arms and tentacles rather than employing the rapid tentacular strike. © 1996 Wiley-Liss, Inc.     

Development and morphology of ciliary urns in the sea cucumber Synaptula hydriformis (Echinodermata: Holothuroidea)

Sea cucumbers (holothuroids) lack the only known echinoderm immune organ, the axial organ. Holothuroids of the families Synaptidae and Chiridotidae have coelomic organs, known as ciliary urns, that gather and excrete waste and, therefore, might function in immunity. Although ciliary urns are widely reported and illustrated in the literature, the process and histology of urn development remain unknown. Development and structure of ciliary urns were examined in Synaptula hydriformis using scanning electron, brightfield, and scanning laser confocal microscopy. Mature urns occurred on all three mesenteries in 10‐tentacled young and later growth stages, and developing urns were found in post‐pentactulae, 10‐tentacled young, and released juveniles. Developing urns were circular clusters of ciliated collar cells protruding from the mesentery. The cells increased in number to form the sessile cushion stage with a shallow lumen. The subsequent spoon‐shaped stage had a stalk and a deepened lumen with an extensive ciliary field where coelomocytes began to accumulate. Mature urns had a thin stalk and cornucopia‐shaped body with an abluminal epithelium of squamous cells and an adluminal epithelium of densely packed ciliated collar cells. Cell boundaries of the rim of mature urns and of the stalk and body of developing urns were outlined on one or both sides by microvilli and an elevated cell membrane. Ciliary urns resembling the cushion‐stage urns of S. hydriformis have been described in the sea star Archaster typicus. If urns in these groups are homologous, it is likely that cushion urns are plesiomorphic and that they are present and have been overlooked in other echinoderms.     

The sensory epithelium of the tentacles and the rhinophore of Nautilus pompilius L. (cephalopoda, nautiloidea)

Nine intraepithelial ciliated cell types that are presumed to be sensory cells were identified in the epithelium of the pre- and postocular tentacles, the digital tentacles, and the rhinophore of the juvenile tetrabranchiate cephalopod Nautilus pompilius L. The morphological diversity and specialization in distribution of the different ciliated cell types analyzed by SEM methods suggest that these cells include receptors of several sensory functions. Ciliated cell types in different organs that show similar surface features were combined in named groups. The most striking cell, type I, is characterized by a tuft of long and numerous cilia. The highest density of this cell type occurs in ciliary fields in the epithelium of the lamellae of the pre- and postocular tentacles, in the olfactory pits of the rhinophores, and in the lamellae of four pairs of lateral digital tentacles, but not in the epithelium of the medial digital tentacles. The similar morphological data, together with behavioral observations on feeding habits, suggest that this cell type may serve in long-distance chemosensory function. The other ciliated cell types are solitary cells with specific spatial distributions in the various organs. Cell types with tufts of relatively short, stiff cilia (types III, IV, VIII), which are distributed in the lateral and aboral areas of the tentacles and at the base of the tentacle-like process of the rhinophore, are considered to be employed in mechanosensory transduction, while the solitary cells with bristle-like cilia at the margin of the ciliary fields (type II) and at the base of the rhinophore (type IX) may be involved in chemoreception. Histological investigation of the epithelium and the nerve structures of the different organs shows the proportion and distribution of the sensory pathways. Two different types of digital tentacles can be distinguished according to their putative functions: lateral slender digital tentacles in four pairs, of which the lowermost are the so-called long digital tentacles, participate in distance chemoreception, and the medial digital tentacles, whose terminal axial nerve cord may represent a specialized neuromechanosensory structure, appear to have contact chemoreceptive abilities.     

Electron microscopic study on the gill bars of amphioxus (Brachiostoma californiense) with special reference to Neurociliary control

Summary Both primary and secondary (tongue) bars of the pharyngeal gill basket are covered by epithelial cells that are continuous with the cells that line the atrium. Anterior and posterior faces of the gill bars are covered with lateral ciliated cells, which possess a single cilium, ringed by microvilli, and an elaborate basal mitochondria-rootlet apparatus. Pharyngeal faces of the gill bars are covered with ciliated pharyngeal cells, atrial faces by mucus secreting atrial cells. The surface epithelium rests on a stromal septum, a flattened tube of basal lamina which dilates to form the visceral blood vessel (along the pharyngeal face) and skeletal blood vessel (along the atrial face). This basal lamina surrounds paired skeletal rods which run through the longitudinal axis of the gill bars near the atrial face. Between the skeletal rods and atrial cells of primary gill bars is a coelomic channel lined by epithelioid coelomic cells. Neuronal processes, some with neurosecretory granules, are located among the bases of the atrial cells. Some axons may contact lateral ciliated cells where the latter meet atrial cells, but synaptoid endings have not been found here or elsewhere in the gill bars. Nervous tissue has not been identified among lateral ciliated cells even though ciliary activity of these cells is supposedly regulated by atrial nervous tissue.Supported by a Cottrell College Science Program Grant from Research Corporation. We thank Nancy Kelly and Gerhard Ott for excellent technical assistance and are grateful for the facilities provided by the Department of Zoology and Seaver Science Center, Pomona College.     

Fine structure of the coelomic epithelium of Sagitta elegans (Chaetognatha)

Summary The coelomic space in the trunk of the arrow worm Sagitta elegans is lined by a thin epithelium, which may be termed coelomic epithelium. The visceral part of this epithelium is composed of flat cells characterized by thin and thick myofilaments, which constitute the circular musculature of the gut. In addition mitochondria, rough ER, and smooth walled cisterns, as well as vesicular and granular inclusions occur; the apical and basal plasma membranes exhibit no particular specializations. The parietal epithelium is exceedingly thin and covers the muscle cells of the body wall. In the lateral fields columnar ciliated cells are to be found which are rich in rough ER cisterns and which apparently are also coelomic epithelial cells.     

Ultrastructure of the coelom in the brachiopod Lingula anatina

The organization of the coelomic system and the ultrastructure of the coelomic lining are used in phylogenetic analysis to establish the relationships between major taxa. Investigation of the anatomy and ultrastructure of the coelomic system in brachiopods, which are poorly studied, can provide answers to fundamental questions about the evolution of the coelom in coelomic bilaterians. In the current study, the organization of the coelom of the lophophore in the brachiopod Lingula anatina was investigated using semithin sectioning, 3D reconstruction, and transmission electron microscopy. The lophophore of L. anatina contains two main compartments: the preoral coelom and the lophophoral coelom. The lining of the preoral coelom consists of ciliated cells. The lophophoral coelom is subdivided into paired coelomic sacs: the large and small sinuses (= canals). The lining of the lophophoral coelom varies in structure and includes monociliate myoepithelium, alternating epithelial and myoepithelial cells, specialized peritoneum and muscle cells, and podocyte‐like cells. Connections between cells of the coelomic lining are provided by adherens junctions, tight‐like junctions, septate junctions, adhesive junctions, and direct cytoplasmic bridges. The structure of the coelomic lining varies greatly in both of the main stems of the Bilateria, that is, in the Protostomia and Deuterostomia. Because of this great variety, the structure of the coelomic lining cannot by itself be used in phylogenetic analysis. At the same time, the ciliated myoepithelium can be considered as the ancestral type of coelomic lining. The many different kinds of junctions between cells of the coelomic lining may help coordinate the functioning of epithelial cells and muscle cells.     

Ultrastructure of coelomic lining in echinoderm podia: significance for concepts in the evolution of muscle and peritoneal cells

Summary Ultrastructural data are presented on the histological organization of coelomic lining in the podia of ten species of the five major groups of extant echinoderms. Further evidence of the incorporation of podial retractor muscle cells (myocytes) into a monociliated myoepithelial coelomic lining is provided. In the podia of the crinoid Nemaster rubinginosa and the ophiuroid Ophiophragmus wurdemani as well as in the feeding tentacles of the holothurian Leptosynapta tenuis, coelomic linings are organized as simple myoepithelia consisting of non-contractile peritoneal cells (peritoneocytes) and myocytes. Coelomic linings in the holothurian Thyonella gemmata, the echinoids Eucidaris cf. tribuloides and Lytechinus variegatus, and the asteroids Asterias forbesi and Astropecten sp. are pseudostratified or bipartite pseudostratified myoepithelia consisting of subapical myocytes and apically situated peritoneocytes. The ophiuroid podia of Ophioderma brevispinum and Ophiothrix angulata exhibit transitions from simple myoepithelia to partially pseudostratified epithelia. Intermediate forms between the extremes in myoepithelial organization also occur in the podial lining of single species (e.g. Eucidaris cf. tribuloides). These data supplement recent ultrastructural studies on the podial lining of echinoderms and, in conjunction with published ultrastructural data on the myoepithelial organization of other coelomic linings in echinoderms and in other coelomates, suggest myoepithelial organization of the coelomic lining is a plesiomorph feature in Bilateria.