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Recent molecular data suggest that the Porifera is paraphyletic (Calcarea+Silicea) and that the Calcarea is more closely related to the Metazoa than to other sponge groups, thereby implying that a sponge-like animal gave rise to other metazoans. One ramification of these data is that calcareous sponges could provide clues as to what features are shared among this ancestral metazoan and higher animals. Recent studies describing detailed morphology in the Calcarea are lacking. We have used a combination of microscopy techniques to study the fine structure of Sycon coactumUrban 1905, a cosmopolitan calcareous sponge. The sponge has a distinct polarity, consisting of a single tube with an apically opening osculum. Finger-like chambers, several hundred micrometers in length, form the sides of the tube. The inner and outer layers of the chamber wall are formed by epithelia characterized by apical–basal polarity and occluding junctions between cells. The outer layer—the pinacoderm—and atrial cavity are lined by plate-like cells (pinacocytes), and the inner choanoderm is lined by a continuous sheet of choanocytes. Incurrent openings of the sponge are formed by porocytes, tubular cells that join the pinacoderm to the choanoderm. Between these two layers lies a collagenous mesohyl that houses sclerocytes, spicules, amoeboid cells, and a progression of embryonic stages. The morphology of choanocytes and porocytes is plastic. Ostia were closed in sponges that were vigorously shaken and in sponges left in still water for over 30 min. Choanocytes, and in particular collar microvilli, varied in size and shape, depending on their location in the choanocyte chamber. Although some of the odd shapes of choanocytes and their collars can be explained by the development of large embryos first beneath and later on top of the choanocytes, the presence of many fused collar microvilli on choanocytes may reflect peculiarities of the hydrodynamics in large syconoid choanocyte chambers. The unusual formation of a hollow blastula larva and its inversion through the choanocyte epithelium are suggestive of epithelial rather than mesenchymal cell movements. These details illustrate that calcareous sponges have characteristics that allow comparison with other metazoans—one of the reasons they have long been the focus of studies of evolution and development.
The symbiotic association between the new sponge species Mycale vansoesti and the coralline alga Amphiroa sp. from the Bunaken Marine Park (North Sulawesi, Indonesia) is described. The alga completely pervades the sponge. The color of the sponge ectosome is white, both on the external surface and on the atrial wall, but where the alga is present the sponge takes on the light pink color of the alga. The sponge spicular complement is characterized by mycalostyles, anisochelae of two types, sigmas (often “C” shaped), and extremely abundant toxas organized in bundles forming toxadragma. In the association, the sponge shows very low silicate value, and consequently the alga represents the main skeleton of the sponge. On the other hand, the sponge affects the morphology of the alga, leading to a cylindrical shape, with thalli running parallel to the sponge surface. This association seems to be obligate for the sponge, as we found no sponges of this species living in isolation.
The epidermis of the free-living typhloplanids Mesostoma viaregginum and M. productum (Mesostominae) is described. In both species, the epidermis has polarized cells with nuclei located at the basal part of the cell, whereas mitochondria are in the apical one. The epidermis is entirely covered by microvilli and locomotory cilia anchored in the cytoplasm by vertical and horizontal rootlets. Rootlets exhibit distinct length and periodic structure in the two species. Furthermore, in each species vertical and horizontal rootlets possess different periodic structure. The pattern of termination of microtubules in epidermal cilia is described for the first time in the Typhloplanida; central microtubules shift along one axonemal side, doublets 1 and 6–9 lose their microtubule B, and gradually peripheral doublets become singlets. Finally, an electron-dense material caps the tip of the cilia. This pattern of termination closely resembles that of Temnocephalida, Kalytorhynchia, and Dalyelliida examined so far, but differences exist.
Life cycles, ploidy levels, reproductive modes, and regeneration capacities of laboratory populations of the southern Brazil freshwater planarians Girardia tigrina and Girardia schubarti were studied. The mating behavior and life cycle of different populations from both species were analyzed regarding their karyotype, body size, modes of reproduction, and regeneration potential. Reproduction was evaluated according to fecundity, fertility, and fissiparity indices. In both species we observed that diploid planarians are ∼25% larger than triploid or mixoploid ones and that sexually reproducing populations have more offspring than asexual ones. Cocoon incubation time was shorter for G. tigrina, and G. schubarti showed a higher frequency of spontaneous malformations. G. tigrina was both more fecund (produced more cocoons) and more fertile (produced more hatchlings) than G. schubarti. The effects of alternative food sources (liver or egg yolk), demographic density, and water–salt concentration were evaluated in different populations of both species. All evaluated environmental factors had effects on fecundity and fertility indices and were more prominent for G. schubarti than for G. tigrina. Our data suggest that the populations of G. schubarti were more sensitive to environmental factors, and thus may be useful as bioindicators.
Many cryptobranch dorid nudibranchs contain innumerable calcareous spicules, yet the function of these elements is unknown. Two possible roles are defense against predators and structural support. In one dorid, Cadlina luteomarginata, whole-mount and thin-section staining revealed an intricate network of spicule tracts and connective tissue ramifying throughout the body, with muscle fibers associated with this spicule/connective tissue matrix and inserting into it. Spicules were present in high concentrations in all areas of the body, but highest in exterior mantle tissue. Relative investment increased isometrically with body size for most body regions, in contrast to the positively allometric investment seen in prosobranch shells. Bioassays with artificial food indicated that spicules alone did not deter generalist crabs and anemones, and only weakly increased the deterrence of secondary chemicals to anemones. Thus, while nudibranch spicules may serve as a defense against other predators, their primary role may be in body support.
Stirpulina ramosa is the only extant endobenthic representative of the Clavagellidae and is restricted to the waters of Japan. A single intact adventitious tube of this species has been obtained and its structure is described. The right valve is 16 mm long and located within the adventitious tube. It has an opisthodetic ligament located on resilifers. There are anterior and posterior adductor muscle scars, a thick pallial line, and pallial and pedal gape (right valve only) sinuses. The left shell valve is but 9 mm long and is united into the fabric of the adventitious tube via the intermediary of a shelly saddle. Internally, only the anterior adductor muscle scar and a small element of the pallial line scar are identifiable on the left valve. The posterior adductor and the rest of the pallial line scar (including a pallial sinus) are, remarkably, located on the adventitious tube beyond the shell valve margin. The adventitious tube of S. ramosa is formed in a manner wholly dissimilar from that of Brechites vaginiferus (Penicillidae). In B. vaginiferus, the tube is secreted as a single entity from the general outer mantle surface, including the siphons, covering the body. As a consequence, both shell valves are incorporated into the structure of the tube and the watering pot is bilaterally symmetrical. In S. ramosa, the tube and watering pot are secreted from the mantle margin and surface surrounding and extending from the left shell valve, so that only the left valve is incorporated into its structure. A dorsally derived mantle element is progressively extended over to the right side of the body, meeting a ventrally derived counterpart that passes beneath it, forming a pleat in the calcareous structure of the right side of the tube that they secrete. This pleat extends into the complex of watering-pot tubules and forms the pedal gape. The watering pot is thus Ω shaped. The ventrally derived mantle element forms a sinusoidal crest on the right-hand base of the watering pot, creating a pedal gape sinus scar on the right valve. The Clavagellidae radiated widely in the Mesozoic, leaving behind a rich fossil record for Stirpulina. Only S. ramosa, however, has survived until the present. In contrast, the Cenozoic Penicillidae has a poor fossil record, but there is a rich variety of extant endobenthic watering-pot shells. It has been argued hitherto that the two families represent a remarkable example of convergent evolution. In view of the success of the Penicillidae and thus the endobenthic, tube-dwelling lifestyle, however, it is hard to understand why Stirpulina has largely died out—even S. ramosa being known by but one or two specimens. A study of the anatomy of S. ramosa might one day answer this question.
We report the results of a laboratory study of the aestivation of Hormogaster elisae to determine the nature of the inactive period (diapause or quiescence) and to evaluate the influence of soil moisture, temperature, season, and earthworm body weight on the process. The results showed that specimens of H. elisae underwent facultative diapause—paradiapause—characterized by the construction of aestivation chambers in which the animal coils up and its activity decreases. Soil moisture appeared to be the most important environmental factor involved in the onset of aestivation. Temperature and time of year also had some influence, but earthworm body weight appeared to have none. Aestivating earthworms showed a decrease of 41.6% in mean body weight. Once replaced in soil with 20% moisture content, they took 6.4±3.1 d to exit their chambers and another 6.5±3.6 d to recover their initial body weight.
Osmotic stress associated with the freshwater environment and desiccation stress associated with the terrestrial environment may have a shortening effect on the length of the innervation of crustacean aesthetascs. Physical stress of the littoral environment may have a similar effect on the length of the cuticular portion of aesthetascs. The aesthetascs of crustaceans that inhabit these environments share a similar ultrastructural feature, which may help animals cope with these environmental stresses. This ultrastructural feature, the position of the basal bodies proximal to the lumen of the aesthetasc, is absent from the aesthetascs of crustaceans that occur in the typical marine environment. Interestingly, the ultrastructural feature associated with these stressful habitats is present in the peduncular aesthetascs of the remipede Speleonectes tanumekes, even though the environmental stresses that may invoke the reduction of aesthetascs are absent in the marine-cave environment where this animal occurs. The importance of the sensitivity of aesthetascs for survival in this lightless environment may result in a selective pressure that favors basal bodies to be positioned proximal to the lumen of the aesthetasc.
In many ways, the apposition eye of the erotylid fungus beetle Neotriplax lewisi resembles that of chrysomelids: its 400–500 mostly hexagonal ommatidia are of the acone type and possess “open rhabdoms,” a tapetum is not present, and axons penetrate the basement membrane in distinct bundles of eight. The eye also shows some unusual features that, at present, defy clear functional interpretation. Firstly, the cuticle of the interfacetal areas stains differently from that of the corneal lenses and, secondly, the two rhabdom systems in each ommatidium (central and peripheral) both possess microvilli that are oriented in such a way as to permit e-vector discrimination. On the basis of comparisons with other open rhabdom eyes, it is postulated that vision in N. lewisi involves neither high resolving power nor superior absolute sensitivity. However, this beetle can distinguish illuminated from shaded areas, and seems specialized to make use of sky polarization (probably in the UV and green regions of the spectrum) and/or the position of the sun as a course-stabilizing function during flights.
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