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 feeding activity of Echinostrephus molaris (de Blainville) in the central red sea

Echinostrephus molaris (de Blainville) is a small Indo‐pacific echinoid which burrows in coral reef limestone. Normally individuals do not leave the burrows so they cannot graze on algae growing around the burrow mouth. E. molaris catches floating algal particles with its long aboral spines. When a particle touches one of these organs or a tube‐foot in the area, the surrounding spines converge and grip it. Captured fragments are lowered to the test by further tube‐foot and spine action and are then passed across the ambitus towards the mouth. They are held by the oral tube‐feet and the shorter curved oral spines which aid ingestion. The behavioural and structural modifications shown for this habit are discussed. Burrowing and particle collecting have allowed E. molaris to occupy a particular niche on the reef. A similar method of food gathering is reported for Echinometra mathaei (de Blainville).     

The role of external appendages in the distribution and life habits of the sand dollar Echinarachnius parma (Echinodermata: Echinoidea)

The action of the aboral podia is one of the key factors controlling the wide distribution of the clypeasteroid Echinarachnius parma. According to field and laboratory studies (Gulf of Maine), E. parma gathers and selects food primarily from its aboral surface, which is naturally orientated just below the nutrient rich, uppermost sediment layer. Compared to Mellita , wider spacing between the aboral spines in E. parma permits silt and larger particles to be ingested and the action of podia allows it to burrow, and thus gather food, in a wider range of sediments. The broad ecologic tolerance of E. parma rather than specialization, facilitated the biological success of this species. The variation in arrangement of podia on the tests of clypeasteroids suggests interspecific differences in feeding and burrowing strategy.     

From competent larva to exotrophic juvenile: a morphofunctional study of the perimetamorphic period of Paracentrotus lividus (Echinodermata, Echinoida)

 The perimetamorphic period in Paracentrotus lividus lasts for 8–12 days. It starts from the acquisition of larval competence, includes the change in form (metamorphosis) and the endotrophic postlarval life, and stops with the appearance of the exotrophic juvenile. All major postlarval appendages already occur in competent larvae being either grouped into the echinoid rudiment (terminal plates, early spines and primary podia) or scattered within the larval integument (genital plates and sessile pedicellariae). Competent larvae show particular behaviour which brings them close to the substratum. The latter is tested by primary podia protruding through the vestibular aperture of the larva. Primary podia are sensory–secretory appendages that are deprived ampullae. They are able to adhere to the substratum in order to allow evagination of the echinoid rudiment (i.e. metamorphosis) and substatum adhesion of the postlarva. Particular spines are borne by the postlarva; these are multifid non-mobile appendages forming a kind of protective armour. Like those of the larva, all characteristic structures of the postlarva (primary podia, multified spines and sessile pedicellariae) are transitory and regress either at the end of postlarval life (primary podia) or during early juvenile life (multifid spines and sessile pedicellariae). Other appendages that develop during postlarval life (i.e. podia with ampulla, point-tipped spines and sphaeridiae) are similar to those borne by the adults and become functional when the individual enters its juvenile life. Thus, the perimetamorphic period appears to be a fully fledged period in the life-cycle of P. lividus, and presumably in the life-cycle of any other sea-urchin species. Accepted: 7 October 1997     

Podial sensory receptors and the induction of metamorphosis in echinoids

Larvae of Strongylocentrotus droebachiensis (Müller), Lytechinus pictus (Verrill), and Lytechinus variegatus (Leske) which are competent to metamorphose display what appears to be substratum-testing behavior prior to metamorphosis. Larvae cease swimming, partially evert the adult rudiment, and walk about examining the substratum with their five primary podia. Larvae eithe r metamorphose or withdraw their podia and resume swimming to settle again elsewhere. Scanning and transmission electron microscopic examinations of the primary podia revealed sensory receptor cells on the rim and on a conical projection at the center of the podial sucker. Each sensory cell has a single short cilium on its apical surface a axonal process at its base which contributes to the basiepithelial nerve plexus. Mature adults of the same species also have comparable sensory structures on their tube feet suckers. It is suggested that the sensory receptors on the primary podia of setting larvae, although they are not specialized larval structures, may be involved in the perception of tactil e stimuli which have been previously demonstrated to be involved in the induction of metamorphosis.     

Neuroanatomy of the tube feet and tentacles in Holothuria glaberrima (Holothuroidea, Echinodermata)

Echinoderms are a key group in understanding the evolution of the nervous system in the Metazoa. Remarkably, little is known about echinoderm neurobiology. The echinoderm podia, which are unique echinoderm modifications and comprise structures responsible for locomotion and feeding, have been largely neglected in nervous system studies. Here, we have applied immunohistological approaches using different neuronal markers to describe the neuroanatomy of the holothurian podia and its relation to the muscular component. We show, using the sea cucumber Holothuria glaberrima (Selenka, 1867), the direct innervation of the podia by the ectoneural component of the nervous system, as well as the existence of a connection between the nervous system components in the main nerves, the muscle, and the connective tissue. These findings confirm the ectoneural origin of the tube feet’s main nervous system and demonstrate its neuroanatomic complexity. We also show the presence of fibers and neurons within the tube feet mesothelium and connective tissue. The study of these simple structures will help us elucidate the echinoderms’ neuromuscular circuit and their evolutionary relationships.     

Localization and distribution of nitric oxide synthase and other neuronal markers in the podia of Holothuria arguinensis

The organization of the nervous system of the holothurian podia—the tentacles, papillae, and tube feet—is still poorly understood, which limits the development of functional studies. Knowledge of nitric oxide (NO) signaling in sea cucumbers is nonexistent, although it is known to play an important role in many essential biological functions, including neurotransmission, throughout the animal kingdom. The objective of this study was to characterize the holothurian podia in Holothuria arguinensis. To this end, we used classical histology, nitric oxide synthase (NOS) distribution, using NADPH‐diaphorase histochemistry and NOS immunostaining, and neuronal immunohistochemistry. Our results revealed an abundant distribution of NO in the nervous components of the holothurian podia, suggesting an important role for NO as a neuronal messenger in these structures. Nitrergic fibers were intensely labeled in the longitudinal nerve and the nerve plexus surrounding the stem, but were more weakly labeled in the mesothelium. NOS was also found in scattered cell bodies and abundant fibers in the podia terminal end (i.e., the discs in tentacles and tube feet, and the pointed conical structures in the papillae), with evident neuronal projections to the bud surface, especially in the tentacles. The podia terminal end was the most specialized area and was characterized by a specific nervous arrangement, consisting of a distinct nerve plate, rich in cells and fibers containing potential sensory cells staining positively for neuronal markers, which makes this the most likely candidate to be a chemosensory region and an important candidate for future exploration.     

Tissue Regeneration and Biomineralization in Sea Urchins: Role of Notch Signaling and Presence of Stem Cell Markers

Echinoderms represent a phylum with exceptional regenerative capabilities that can reconstruct both external appendages and internal organs. Mechanistic understanding of the cellular pathways involved in regeneration in these animals has been hampered by the limited genomic tools and limited ability to manipulate regenerative processes. We present a functional assay to investigate mechanisms of tissue regeneration and biomineralization by measuring the regrowth of amputated tube feet (sensory and motor appendages) and spines in the sea urchin, Lytechinus variegatus. The ability to manipulate regeneration was demonstrated by concentration-dependent inhibition of regrowth of spines and tube feet by treatment with the mitotic inhibitor, vincristine. Treatment with the gamma-secretase inhibitor DAPT resulted in a concentration-dependent inhibition of regrowth, indicating that both tube feet and spine regeneration require functional Notch signaling. Stem cell markers (Piwi and Vasa) were expressed in tube feet and spine tissue, and Vasa-positive cells were localized throughout the epidermis of tube feet by immunohistochemistry, suggesting the existence of multipotent progenitor cells in these highly regenerative appendages. The presence of Vasa protein in other somatic tissues (e.g. esophagus, radial nerve, and a sub-population of coelomocytes) suggests that multipotent cells are present throughout adult sea urchins and may contribute to normal homeostasis in addition to regeneration. Mechanistic insight into the cellular pathways governing the tremendous regenerative capacity of echinoderms may reveal processes that can be modulated for regenerative therapies, shed light on the evolution of regeneration, and enable the ability to predict how these processes will respond to changing environmental conditions.     

Morphological evolution of newly metamorphosed sea urchins--a phylogenetic and functional analysis

Newly metamorphosed juvenile sea urchins are highly variable across taxa. This contribution documents and illustrates structural, functional, and phylogenetic variation among newly metamorphosed juvenile sea urchins for 31 species from 12 ordinal or familial lineages. The classic juvenile with five primary podia, 20 interambulacral spines, and variable numbers of juvenile spines is found commonly among new metamorphs across lineages, but there are many examples, which depart from this pattern and most likely reflect adaptation to settlement habitats. At metamorphosis juveniles can have 5-25 functional podia. They can have 0-65 spines, 0 or 5 sphaeridia (balance organs). They may have zero or up to eight pedicellariae. While competent larvae that delay metamorphosis may continue to develop juvenile structures, variation across species is much greater than within species and there are strong phylogenetic and functional differences among juveniles. Heterochronic changes in expression of these structures can account for differences among taxa. Based on this sample, juvenile characters such as spines, podia, and larval pedicellariae are expressed in ways that suggest they are developmental modules whose expression can be readily changed relative to one another and to the time of metamorphosis.     

Comparative histological and immunohistochemical study of sea star tube feet (Echinodermata, Asteroidea)

Adhesion in sea stars is the function of specialized structures, the tube feet or podia, which are the external appendages of the water-vascular system. Adhesive secretions allow asteroid tube feet to perform multiple functions. Indeed, according to the sea star species considered, the tube feet may be involved in locomotion, fixation, or burrowing. Different tube foot shapes usually correspond to this variety of function. In this study, we investigated the variability of the morphology of sea star tube feet as well as the variability of the composition of their adhesive secretions. This second aspect was addressed by a comparative immunohistochemical study using antibodies raised against the adhesive material of the forcipulatid Asterias rubens. The tube feet from 14 sea star species representing five orders and 10 families of the Class Asteroidea were examined. The histological study revealed three main tube foot morphotypes, i.e., knob-ending, simple disc-ending, and reinforced disc-ending. Analysis of the results suggests that tube foot morphology is influenced by species habitat, but within limits imposed by the evolutionary lineage. In immunohistochemistry, on the other hand, the results were very homogeneous. In every species investigated there was a very strong immunolabeling of the adhesive cells, independently of the taxon considered, of the tube foot morphotype or function, or of the species habitat. This indicates that the adhesives in all the species considered are closely related, probably sharing many identical molecules or, at least, many identical epitopes on their constituents.     

Histopathology of the disease causing mass mortality of sea urchins (Strongylocentrotus droebachiensis) in Nova Scotia

The disease causing mass mortalities of Strongylocentrotus droebachiensis off Nova Scotia, Canada, from 1980 to 1983 is described. Diseased urchins were characterized by loss of preipheral muscle function in tube feet, spines, and mouth. Signs occurred primarily in the body wall and associated tissues (water vascular system, nerves, spine bases) and coelomic fluid. These symptoms were diffuse and included a general infiltration of tissues with amoebocytes. The coelomic fluid often contained reduced numbers of red and white spherule cells, and clotting was incomplete. Progressive breakdown and fragmentation of muscle cells in tube feet and spine bases resulted in destruction of coherent muscle layers and their replacement by numerous spindle-shaped fibrillar muscle remnants. Coelomic lining cells in the tube feet sloughed off into the lumen, but remained in clumps and phagocytosed muscle remnants.     

Observations on the clypeasteroid Echinocyamus pusillus (O. F. Müller)

The tiny echinoid Echinocyamus pusillus (O. F. Müller) is equipped with specialized external structures that suit it for a wide variety of environments. Special features include the ability to burrow in sediments of fine sand to shell gravel and to climb vertically.Specimens dredged off the west coast of Scotland were observed in aquaria and with the SEM. E. pusillus is characterized by three kinds of spines, and by two of pedicellariae. In contrast to sand dollars, the spines play a passive rôle in the feeding and burrowing operation, probably retaining a defensive nature as in the regular urchins. It is the podia that are chiefly involved in climbing, burrowing, righting, and probably feeding. Surface ciliary currents transport particles, but not to the mouth; they may have a respiratory or cleansing function. Experimental animals did not burrow in either very fine or very coarse sand, probably because a certain relationship exists between particle weight and podia size.E. pusillus shares behavioural and structural characteristics with regular and irregular urchins. It is not a true sand dollar, but may illustrate an evolutionary stage towards such a form.     

Ultrastructure of the Penicillate Podia of the Spatangoid Echinoid Echinocardium cordatum (Echinodermata) with Special Emphasis on the Epidermal Sensory-Secretory Complexes

The spatangoid echinoid Echinocardium cordatum possesses specialized penicillate podia that handle sediment particles during burrowing and feeding. Epidermal complexes, which occur on podial surfaces directly contacting the sediment, each comprise four cells: a non-ciliated secretory cell containing granules rich in mucopolysaccharides (NCS cell), a ciliated secretory cell containing granules of unknown composition (CS cell), and two ciliated non-secretory cells (CNS cells). The cilium of the CS cell is subcuticular whereas that of each CNS cell traverses the cuticle. We propose that these four cells constitute a sensory-secretory complex wherein the ciliated cells are sensory cells and the secretory cells function for adhesion and de-adhesion. More exactly, an NCS cell adhesive and a CS cell de-adhesive would be sequential and would be initiated by two successive stimulations transduced by cilia when the podium touches the sediment. Cilia that first contact the sediment are those protruding through the cuticle from the CNS cells. Their stimulation would result in the secretion of an adhesive material by the NCS cells. Subsequently, the subcuticular cilia of CS cells would be stimulated when the podial digitations closely squeeze the substrate, and this would induce the secretion of a de-adhesive. These two antagonistic secretions would allow the podium to pick up and discharge sediment repetitively during burrowing and feeding.     

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)     

Feeding behavior of the cirratulid Cirriformia filigera (Delle Chiaje, 1825) (Annelida: Polychaeta).

Observations of the feeding behavior of Cirriformia filigera (Delle Chiaje, 1825) (Annelida: Polychaeta) from the intertidal zone of S?o Francisco and Engenho D'água beaches (S?o Sebasti?o, State of S?o Paulo) were made in the laboratory. This species, like other cirratulids, is a deposit feeder, feeding mainly on sediment surface with the aid of its grooved and ciliated palps, which are used to capture food particles. The worm lies just beneath the substrate surface in a J-shaped tube. When feeding, it extends up to 4 palps over the sediment surface, capturing food particles which pass down the groove of each palp directly to the mouth. Only fine sand grains are ingested. The worm frequently extends 4 branchial filaments into the overlying water for aeration. When it moves with the prostomium sideways, it collects and transports sand grains that pass backwards along its ventral region until reaching the middle part of its body. Next, the parapodia and palps move the sand grains to the dorsal posterior end of the animal, covering this area with sand. Some sand grains are also ingested as the worm moves.     

Tissue and spine regeneration in the temperate sea urchin Psammechinus miliaris

The tissue regenerative capabilities of echinoderms are well known at the morphogenic level, yet significant knowledge gaps remain concerning the molecular control of these processes. This pilot study assayed two pharmacological agents (vincristine sulphate and DAPT) injected directly into the body cavity of specimens of the temperate echinoid Psammechinus miliaris which had had their spines and tube feet deliberately amputated. Vincristine sulphate, which is a generalised mitotic inhibitor, was used as a positive control, whereas DAPT is a y-secretase inhibitor known to block sea urchin embryo development and suppress echinoid regeneration by interfering with Notch signalling pathways. Significant differences in regeneration rate became apparent in both treatments 29 days post amputation with both inhibitors slowing regeneration of tube feet (0.6 μg/g vincristine sulphate by 44.4% relative to controls; 4 μg/g DAPT by 55.6% relative to controls) and spines (0.6 μg/g vincristine sulphate by 53.3% relative to controls; 4 μg/g DAPT by 66.7% relative to controls). Vincristine sulphate was more clearly dose-dependent than DAPT. This initial inhibition-based approach allows inferences to be made concerning possible molecular pathways controlling regeneration within P. miliaris and adds further support to the hypothesis that Notch signalling plays a major role in regulating regeneration in echinoids.     

Walking versus breathing: mechanical differentiation of sea urchin podia corresponds to functional specialization

The podia of sea urchins function in locomotion, adhesion, feeding, and respiration; but different podia on a single urchin are often specialized to one or more of these tasks. We examined the morphology and material properties of podia of the green sea urchin, Strongylocentrotus droebachiensis, to determine whether, despite apparent similarities, they achieve functional specialization along the oral-aboral axis through the differentiation of distinct mechanical properties. We found that oral podia, which are used primarily for locomotion and adhesion, are stronger and thicker than aboral podia, which are used primarily for capturing drift material and as a respiratory surface. The functional role of ambital podia is more ambiguous; however, they are longer and are extended at a lower strain rate than other podial types. They are also stronger and stiffer than aboral podia. In addition, all podia become stronger and stiffer when extended at faster strain rates, in some cases by nearly an order of magnitude for an order of magnitude change in strain rate. This strain-rate dependence implies that resistance to rapid loading such as that imposed by waves is high compared to resistance to slower, self-imposed loads. Thus, the serially arranged podia of S. droebachiensis are functionally specialized along an oral-aboral axis by differences in their morphology and mechanical properties.     

Peristomial tube feet and plates of regular echinoids

Summary Peristomial tube feet, ampullae and plates are described in 16 species of regular echinoids. Two basic arrangements are recognised. In cidaroids and echinothurioids there are many tube feet and ampullae per column and the radial water vessel extends on to the peristomial membrane. Tube feet terminate in a small sensory pad. Ampullae are small and flattened. In other echinoids there are only ten peristomial tube feet and the radial water vessel does not extend on to the peristomial membrane. Tube feet terminate in a broad disc and ampullae are cylindrical tubes. Plate structure and pore morphology also vary and are correlated with tube foot structure. Echinothurioids are considered to be derived from a cidaroid ancestor.     

Constructing and testing hypotheses of dinosaur foot motions from fossil tracks using digitization and simulation

Whilst bones present a static view of extinct animals, fossil footprints are a direct record of the activity and motion of the track maker. Deep footprints are a particularly good record of foot motion. Such footprints rarely look like the feet that made them; the sediment being heavily disturbed by the foot motion. Because of this, such tracks are often overlooked or dismissed in preference for more foot-like impressions. However, the deeper the foot penetrates the substrate, the more motion is captured in the sediment volume. We have used deep, penetrative, Jurassic dinosaur tracks which have been naturally split into layers, to reconstruct foot motions of animals living over 200 million years ago. We consider these reconstructions to be hypotheses of motion. To test these hypotheses, we use the Discrete Element Method, in which individual particles of substrate are simulated in response to a penetrating foot model. Simulations that produce virtual tracks morphologically similar to the fossils lend support to the motion being plausible, while simulations that result in very different final tracks serve to reject the hypothesis of motion and help generate a new hypothesis.     

Key adhesion molecules are present on long podia extended by hematopoietic cells.

BACKGROUND:We recently reported that CD34(+) hematopoietic cells and the KG1a cell line extend long, thin podia. These podia can dynamically extend and retract, often adhere to the substrate, and appear to connect cells up to 300 microm apart. The surface receptors found on these podia have not been described. METHODS:By using time-lapse fluorescent microscoscopy and immunostaining techniques, we describe a method for detecting surface receptors on these podia. This includes an in situ antibody staining procedure without fixing cells. RESULTS:We demonstrate, using CD34 selected mobilized peripheral blood cells and KG1a cells, that adhesion molecules known to play important roles in blood-cell migration and adhesion are present on these podia. These include: CD11a, CD18, CD29, CD34, CD45, CD49d, CD49e, and CD62L. Additionally, CD54 and CD44 were present on the podia extended by KG1a cells, but were not detectable on the primary CD34(+) cells. The integrin CD49d localized at the base of these podia in a time-dependent manner in KG1a cells. The frequency and morphology of these long podia on three myeloid leukemia-cell lines (KG1a, MV4-11, and AML-193) and a CD34-negative T-cell line (CEM) are also compared. KG1a and CEM cell lines extend long, dynamic podia that are similar to the podia on primary CD34(+) cells in morphology and adhesion molecule expression. The AML-193 and MV4-11 cell lines, however, did not extend these long podia. CONCLUSIONS:We describe a technique that provides a method of detecting surface receptors on thin cell membrane projections. These results support the likely role of these podia in cell migration and cell-cell communication.