Choanocyte Chambers Research Articles

Formation and construction of asexual buds of the freshwater spongeRadiospongilla cerebellata (Porifera, Spongillidae)

The buds ofRadiospongilla cerebellata are formed asexually. Budding can be induced experimentally by injuring the sponge. The first sign of budding is a slight elevation of some surface areas, which proceed to rise rapidly so that they soon protrude conspicuously from the surface of the sponge. As a bud develops, the broad base joining it to the mother sponge narrows to a stalk, which finally breaks. The free buds drift in the water for 15–20 min and then settle, forming new sessile sponges. The buds, 1.5–2.5 mm in diameter, have an internal organization identical with that of the mother sponge. They are enclosed in a layer of pinacoderm perforated by dermal pores. Under the pinacorderm there is a shallow subdermal space, which is in communication with the incurrent canals leading to the choanocyte chambers. The water sucked into these chambers proceeds into the excurrent canal system and emerges from the sponge through the oscular tube. Spicules projecting radially from the bud bear apical tufts of microscleres. The skeletal spicules of the buds, like their choanocyte chambers, are smaller than those in the mother sponge. The chambers expand to their mature size by choanocyte mitosis. Buds and sponges are colored green by intracellular symbiotic algae of the genusChlorella.

Comparative study of the choanosome of porifera: II. The keratose sponges.

The aquiferous system of representatives of the orders Dictyocer-atida, Dendroceratida, and Verongida has been studied to note its relevance to the systematics of the groups. The volume of the choanocyte chamber, the size and shape of the choanocytes, the number of choanocytes per chamber, the relative development of the mesohyl, and the features of endopinacocytes are estimated from scanning and transmission electron microscopic observations of representatives of most families of the three orders. Although the Dysideidae have a reticulate skeleton and were classified in the order Dictyoceratida, they are actually closer to the Aplysillidae (Dendroceratida) than to dictyoceratids. The anatomy and cytology of the Halisarcidae differ profoundly from those of these three orders and are clearly more closely related to nonkeratose sponges. Some changes in classification lead to a pattern with highly homogeneous orders that clearly differ in their anatomic and cytologic features, which does not support the hypothesis of a common origin of the "keratose" sponges.

A new type of central cell in the choanocyte chambers of Pellina fistulosa (Porifera, Demospongiae)

Central cells of a hitherto unknown type, forming a continuous, perforated layer at the level of the distal collar ends in each choanocyte chamber, have been found in the choanocyte chambers of Pellina fistulosa. The collars project through the pores of the perforated central cell layer. The spaces between the collar ends and between the collars and the cone cell ring in the apopyle region are sealed by the central cell cytoplasm. The latter represents an impermeable barrier for particulate material as well as for water and thus enhances the filtration efficiency by preventing a bypass of water and particles between the collar apices.

Micromorphology and ultrastructure of Caribbean sclerosponges

Fine structural analysis of living tissue of the sclerosponges Ceratoporella nicholsoni (Hickson) and Stromatospongia norae Hartman, collected near Discovery Bay, Jamaica, between 1984 and 1986, was carried out using transmission and scanning electron microscopy (TEM and SEM). The thick dermal membrane of these sponges is covered by exopinacocytes having a “T” shape in sections perpendicular to the surface. A dense, complex glycocalyx is produced at the surface of these cells. Choanocyte chambers are diplodal and unusually small. The inhalant and exhalant canals of both species are characterized by the presence of valvules, made by transverse lamellipodial processes of the endopinacocytes lining them. An abundant and diversified bacterial community occupies almost 20% of the mesohyl. A single layer of active basopinacocytes lines the mesohyl at the interface between the living tissue and the aragonitic skeleton. Basopinacocytes are presumed to be precursors of the irregular fibrillar organic matrix found in the aragonitic skeleton. Sclerocytes and spongocytes are abundant in the vicinity of the siliceous spicules. Typical lophocytes releasing smooth collagen fibrils are common in the dermal membrane as well as in the choanosome where they can be grouped in bundles. Uniquely, C. nicholsoni elaborates rough intercellular fibrils characterized by periodically spaced thickenings. The endolithic algae Ostreobium sp. is present in the most apical zones of the aragonitic skeleton, but does not seem to interfere with its development. The striking micromorphological resemblances between both species are discussed and compared to demosponges.

Microscopical aspects on symbiosis of Spongilla lacustris (Porifera, Spongillidae) and green algae

When growing in the sunlight, some specimens of Spongilla lacustris are coloured green due to the presence of symbiotic unicellular chlorellae. The algae live inside most sponge cells. The chlorellae were extracted from green sponges, cultivated, added to algae-free sponges and fixed after different incubation times. In this way the uptake of the algae, their distribution and their final whereabouts in the mesenchymatic cells could be followed by in vivo microscopy, phase-contrast microscopy and electron microscopy. A few minutes after addition, the chlorellae can be found inside the choanocyte chambers. Here they are taken up by the cell bodies and collars of the choanocytes. Pinacocytes are also involved in the uptake. The distribution of algae results from a specific transmission from the donor cell to the receiver cell. The chlorellae are not released from their host vacuoles until they are extensively enclosed by the cell taking them up. Six hours after addition, all sponge cells contain algae except granulocytes, microscleroblasts, the pinacocytes of the peripheral rim region and those of the pinacoderm. The chlorellae are able to divide inside the sponge cells.

The architecture of the canal systems of Petrosia ficiformis and Chondrosia reniformis studied by corrosion casts (Porifera, Demospongiae)

The three-dimensional organization of the canal system in two sponge species, Petrosia ficiformis and Chondrosia reniformis, was studied using corrosion casts. Casts were made of live animals, in situ, and canal replicas were analzyed by scanning electron microscopy (SEM). In P. ficiformis the incurrent system consists of a superficial canal network giving rise to large radial canals, which ramify and anastomosize forming an internal web. Excurrent canals are arranged into modular ramified systems radiating from atrial cavities opening to the exterior. Main excurrent canals run at various depths within the sponge, even through the superficial incurrent network. Both incurrent and excurrent canal replicas show smooth, blind-ending capillaries. Some large incurrent canals merge with excurrent ones, thus bypassing choanocyte chambers. In C. reniformis there is a cortical collagen layer crossed by three-like incurrent canals, the “twigs” of which communicate with groups of inhalant pores. The stems of tree-like canals penetrate into the sponge medulla where they ramify and anastomosize to form a web. Main excurrent canals arise from large cloacal ducts leading to the oscular openings. They give rise to a sequence of branches intersecting the incurrent web. Both incurrent and excurrent canals have sharp, blind-ending capillaries. Morphometric data functions show that diameter scaling in canal branches is exponential in Petrosia and linear in Chondrosia. Structural differences and homologies between the two species are discussed.

Canal systems and choanocyte chambers in freshwater sponges (Porifera, Spongillidae)

The spongillid species Spongilla lacustris and Ephydatia fluviatilis possess choanocyte chambers of the classical eurypylous type. They are surrounded by the mesenchymal tissue and connected to the incurrent canal system by prosopyles and to the excurrent canal system by wide apopyles. Each apopyle is sealed against spaces between the basal choanocyte collar parts by a ring of uniflagellated cone cells. The functional aspects of the choanocyte chamber and canal structure are discussed.

Ultrastructural study of spermatogenesis inOscarella lobularis(Porifera, Demospongiae)

Summary The various phases of spermatogenesis in the demosponge Oscarella lobularis were studied by electron microscopy. Spermatogenesis occurs within spermatic cysts, which are presumed to derive from choanocyte chambers by transformation of choanocytes into spermatogonia. Germ cells develop asynchronously within spermatocysts, and cytoplasmic bridges, indicating incomplete cells division, connect several germ cells. Attached spermatogonia suggest gonial generations. Spermatocytes I typically show the presence of synaptonemal complexes indicating meiotic divisions. Spermatocytes II have a small size probably because of the meiotic divisions of spermatocytes I. Spermatids are characterized by an acrosome, a big mitochondrion and a peripheral sheath of condensed chromatin surrounding a clearer central area in the nucleus. The mature spermatozoon shows a lateral flagellum and a flattened acrosome capping the nucleus. The phylogenetic implications of some features of the spermatozoon are suggested.

Body structure of marine sponges

Each choanocyte chamber of Petrosia ficiformis is formed by a slightly outpocked choanocyte epithelium and by a ring of three or four uniflagellated cone cells surrounding the apopyle. The apopyle opens into a small aphodus, which leads the water flow to larger excurrent canals. Pinacocytes of the incurrent canal system cover the basal surface of the choanocytes and separate them from the incurrent canals and the mesenchyme. The water flows into the chambers by pores in the pinacocyte cover and then through gaps between adjacent choanocytes. To our knowledge this is the first report of a leuconoid canal system in which choanocyte chambers are covered by a pinacocyte epithelium of the incurrent canal system that isolates the chambers from the mesenchyme. A future comprehensive revision of the types of canal systems in sponges seems to be necessary.

The uptake of particulate food inReniera sp. (Porifera)

The choanocyte chambers of the marine spongeReniera sp. protrude with their curved outer surface free into the incurrent canals. The water is sucked into the chambers by cavities between the choanocytes. Particles up to 1 µm in diameter may enter the chambers with the water current. These particles are trapped on the outer surface of the choanocyte collars and are ingested by the choanocytes and processes of the pinacocyte epithelium of the incurrent canal system, which project into the chambers. Bigger particles are retained in the incurrent canals mainly on the outer surface of the choanocyte chambers. They are ingested by pinacocytes of the canal wall and transported to cells of the mesenchyme. The present investigation shows the great importance of the pinacocyte epithelium of the incurrent canal system for suspension feeding inReniera sp.

Cortical and endosomal structure of the marine sponge Stelletta grubii

The fine structure of the marine astrophorid sponge Stelletta grubii is described for the first time. The following new data are presented: spongin is present, choanocyte chambers are diplodal, intercellular symbiotic bacteria are numerous and unequally distributed in the cortex and endosome, and collagenous fibril bundles are associated with lophocyte activity and are not elastic fibers. The cortex contains numerous fibril bundles, fewer symbionts, very few cells, and transitional zones with higher archeocyte density near the surface and endosome. Limited phagocytosis of the bacterial symbionts is observed. This species appears to be dioecious and oviparous. These observations suggest that the enigmatic species Chondrosia reniformis is closely related to S. grubii and that it should be placed within or near the astrophorids. The rhizoids of the red alga Phyllophora palmettoides penetrate the sponge tissue without eliciting the development of a structurally specialized contact zone in the sponge matrix or of a limiting epithelium.

Origin of male gametes from choanocytes inSpongia officinalis(Porifera, Demospongiae)

Summary Spermatogenesis in Spongia officinalis takes place within spermatocysts surrounded by follicle cells. Cysts develop asynchronously from choanocyte chambers by transforming choanocytes into gonia. During this process spermatogonia seem to show phagocytic activity by forming pseudopodia surrounding mesohyl bacteria and cytoplasmic vacuoles which contain such microorganisms. Furthermore nuclei shift from the basal zone of the cells to the apical one, while flagella and collars are lost. Thereafter, the nucleus/cytoplasm ratio tends to increase, cytoplasmic inclusions are lost and the flagellum again becomes visible. Primary spermatocytes, identified by the presence of synaptinemal complexes, and the successive stages of spermatogenesis have been followed up to mature spermatozoa. Secondary spermatocytes are often connected by cytoplasmic bridges deriving from incomplete cytodieresis. Such bridges, which are found to connect spermatids too, could play a role in synchronizing sperm maturation.

Comparative study of the choanosome of Porifera: 1. The Homoscleromorpha.

The choanoderm and pinacoderm of representatives of the two families of Homoscleromorpha sponges, the Oscarellidae and Plakinidae, have been examined by transmission and scanning electron microscopy. Different fixative procedures have shown the dramatic influence of fixation conditions on the morphology of choanocytes. These two families of sponges have the following morphological features in common: flagellated endopinacocytes with short apical microvilli and basal pseudopods; the presence of a very thin and dense sheet of matrix material which limits the mesohyl. There are, however, only minor differences in the flagellar morphology, granule content, and anchoring system of their choanocytes. Two findings are of particular interest: (1) the presence of glycocalyx bridges between the microvilli of the choanocyte collar; and (2) the discovery of a new cell type, the apopylar cell, which has a morphology intermediate between that of pinacocytes and choanocytes. The apopylar cells limit the apopylar opening of the choanocyte chamber and indicate the transition between choanoderm and pinacoderm.

Fossil Hexactinellida

The structure and evolution of the hexactinellid skeleton has been conditioned by: (1) the rectangular form of the spicule (ultimately due to the square cross-section of the axial canal), and (2) the sheet-like form of the choanocyte-membrane, properly the choano-syncytium (Reiswig, 1979) as individual choanocytes with proper nuclei do not exist, which is a continuous syncytial sheet bearing outpocketings (diverticula) that correspond to the choanocyte chambers of other sponge groups. In most species the diverticula are separate, and attached to one another by syncytial filaments, but their arrangement as part of a sheet-like structure is still apparent. In a few species the choanocyte membrane becomes a labyrinth of anastomosing tubes. Accompanying these are the essential absence of mesogloea and the paucity of collagen (spongin), which results in the soft parts being essentially confined to the space occupied by the skeleton. The place of mesogloea is taken by a syncytial network of filaments which also form the dermal and gastral membranes.

Ultrastructural study of differentiation processes during aggregation of purified sponge archaeocytes.

Archaeocytes from the spongeEphydatia fluviatilis were dissociated and then isolated on Ficoll density gradients. Their aggregation and reconstitution processes were studied by transmission electron microscopy to determine their capabilities for differentiation.Archaeocyte aggregates follow a well defined sequence of differentiation to generate the characteristic structures of a sponge. Pinacoderm is the first structure to be regenerated and appears progressively at the surface of the 12 h aggregates. Pinacocytes which have differentiated in archaeocyte aggregates are identical to native ones except that the nucleolus remains in most cells. The choanocytes appear only after 24 h by a two step process. First, small cells (choanoblasts) are formed from archaeocytes by mitosis. These cells then transform into fully differentiated choanocytes possessing collars and flagella. The early choanocyte chambers are small, irregular and randomly dispersed in the aggregates. Finally, collencytes and sclerocytes begin to appear just before the aggregates spread on the substrate.The differentiation of a suspension of pure archaeocytes is a unique model system to study sponge cell differentiation and has allowed us to demonstrate that archaeocytes isolated from developed sponges maintain the capacity to differentiate even though this capacity is not usually expressed.

Microbial associations in sponges. I. Ecology, physiology and microbial populations of coral reef sponges

Illumination, current strength and physical turbulence influence the distribution of 4 tropical sponges. Three sponges with cyanobacteria in exposed tissues grow only in poen shallow habitats: Pericharax heteroraphis in moderate-current, lowturbulence regions on the reef slope; Jaspis stellifera in low-current, moderate-turbulence regions of the outer reef flat; and Neofibularia irata in moderate-current, high-turbulence areas below the reef crest. Ircinia wistarii contains no cyanobacteria and occurs in deeper, strong-current, high-turbulence regions. N. irata agressively overgrows neighbouring corals and its growth form is influenced by the current strength. The sponges efficiently filter bacteria from the water. The efficiency is related to the aquiferous structure, particularly the size of choanocyte chambers, and is unrelated to the existing bacterial populations in sponge tissue. The numbers of bacteria associated with the sponges are proportional to the sponge mesohyl density, with the dense sponges J. stellifera and I. wistarii containing many bacteria whereas P. heteroraphis is not dense and has few bacteria.

The central cells of sponges

Twenty-one species of Porifera have been surveyed by light microscopy for the presence, form, and relative abundance of a little known cell type known as central cells. They are found to be present in fifteen of these species and occur in six morphologically recognizable forms. Their functional roles are reinterpreted in the light of new distributional and abundance data. The central cells of the siliceous ceractinomorph demosponges are common and intimately associated with the choanocyte population. They probably play an important role in control of water currents within individual choanocyte chambers to mediate cleaning of the outer chamber surfaces. The central cells of keratosan and tetractinomorph demosponges appear to represent stages in egestive processes of wandering mesenchyme cells.

Hydroxyurea: An Inhibitor of the Differentiation of Choanocytes in Fresh-Water Sponges and a Possible Agent for the Isolation of Embryonic Cells

During the development of a fresh-water sponge from its gemmules, most cell types originate from the undifferentiated archaeocytes through a few divisions, whereas each choanocyte chamber, composed of several tens of choanocytes, arises from a single archaeocyte through repeated mitoses. This process was studied on gemmules incubated in various concentrations of hydroxyurea. A concentration of 100 μg/ml postponed the hatching by about two days, and blocked the differentiation of the choanocytes and the morphogenesis of the aquiferous system. The resulting organism was a hollow dome of pinacoderm, stretched on spicules, the bottom of which was strewn with embryonic archaeocytes. After washing and incubation in mineral medium, the sponge differentiated its choanocytes and achieved normal development. The incorporation of 3 H-thymidine into DNA was compared throughout the development of normal and hydroxyurea-treated gemmules. Hydroxyurea delayed the first peaks of incorporation and abolished the large peak that normally occurs around 90 h, just before the formation of choanocyte chambers. When added after 96 h incubation, hydroxyurea did not affect the differentiation of the choanocytes. These results suggest that the differentiation of the choanocytes and the further morphogenesis of the aquiferous system depend on the repetitive divisions of the archaeocytes that normally occur around 90 h. Furthermore, hydroxyurea-blocked sponges provide a suitable source for the isolation of pure populations of embryonic archaeocytes.

The aquiferous systems of three marine demospongiae.

The aquiferous systems of three common, coastal, marine Demospongiae, Halichondria panicea (Pallas), Haliclona permollis (Bowerbank) and Microciona Prolifera (Ellis and Solander), are analyzed by measurements of cross-sectional areas of conducting elements. The patterns in demosponges of extremely different organizational morphologies are found to be quantitatively similar. The porocyte nature of the ostia is established for all three species. Choanocyte chamber densities range from 1 to 1.8 × 107 chambers ml-1 with 57 to 95 choanocytes per chamber (means). Cross-sectional area of the intervillar space of the choanocyte collars is calculated to be 12 to 56 times the lateral surface area of the specimen. Velocities of water movement through specific elements of the aquiferous system are calculated from cross-sectional area data and measured oscular flow of Haliclona permollis. The calculated Reynolds numbers lie below the critical value and fluid flow is thus considered laminar throughout the aquiferous systems of these sponges.