The evolution of protonephridia of the Platyhelminthes

Three types of flame bulbs are distinguished in the Platyhelminthes: type 1 has two cilia arising from a terminal cell and rootlets extending along the weir; type 2 has many cilia arising from a terminal cell and the proximal canal cell closely aligned with it; and type 3 has a non-terminal perikaryon forming many flame bulbs, each with many cilia and a single row of longitudinal ribs. Each type appears in various structural forms. Type 1 is found in the Catenulida; type 2 in the Macrostomida, Polycladida, Prolecithophora, Proseriata, Tricladida, Fecampiidae, and Neodermata; and type 3 in the Rhabdocoela and Lecithoepitheliata. The most likely evolutionary sequence is that type 3 is derived from type 2 and, perhaps, that type 2 is derived from type 1. Characters of the protonephridia show that the Rhabdocoela and the Neodermata form separate phylogenetic lineages; other similarities between these taxa are due to convergent evolution (or horizontal gene transfer?).     

Are the Platyhelminthes a monophyletic primitive group? An assessment using 18S rDNA sequences

In most zoological textbooks, Platyhelminthes are depicted as an early- emerging clade forming the likely sister group of all the other Bilateria. Other phylogenetic proposals see them either as the sister group of most of the Protostomia or as a group derived from protostome coelomate ancestors by progenesis. The main difficulty in their correct phylogenetic placing is the lack of convincing synapomorphies for all Platyhelminthes, which may indicate that they are polyphyletic. Moreover, their internal phylogenetic relationships are still uncertain. To test these hypotheses, new complete 18S rDNA sequences from 13 species of "Turbellaria" have been obtained and compared to published sequences of 2 other "Turbellaria," 3 species of parasitic Platyhelminthes, and several diploblastic and deuterostome and protostome triploblastics. Maximum-parsimony, maximum-likelihood, and neighbor-joining methods were used to infer their phylogeny. The results show the order Catenulida to form an independent early- branching clade and emerge as a potential sister group of the rest of the Bilateria, while the rest of Platyhelminthes (Rhabditophora), which includes the parasites, form a clear monophyletic group closely related to the protostomes. The order Acoela, morphologically considered as candidates to be ancestral, are shown to be fast-clock organisms for the 18S rDNA gene. Hence, long-branching of acoels and insufficient sampling of catenulids and acoels leave their position still unresolved and call for further studies. Within the Rhabditophora, our analyses suggest (1) a close relationship between orders Macrostomida and Polycladida, forming a clear sister group to the rest of orders; (2) that parasitic platyhelminthes appeared early in the evolution of the group and form a sister group to a still-unresolved clade made by Nemertodermatida, Lecithoepitheliata, Prolecithophora, Proseriata, Tricladida, and Rhabdocoela; and (3) that Seriata is paraphyletic.      

Adhesive organs of the gastrotricha

Summary Adhesive organs of 17 gastrotrich species of the order Macrodasyida and 2 species of the order Chaetonotida (Chaetonotida-Paucitubulatina) can be seen by transmission electron microscopy to comprise two gland cell types. These cells are morphologically similar to viscid and releasing glands of the Turbellaria and so are identified by these same names; the adhesive system in these gastrotrichs is therefore called a duo-gland system considered at least functionally comparable to the duo-gland organs of turbellarians. The two gland cell types project their necks through tubiform extensions of the animal's cuticle. Some adhesive tubules have only one of each gland type; others, even in the same species, may have two viscid and one releasing glands; and compound organs such as posterior footlike appendages may have three and four viscid glands and one releasing gland per tubule. Gland cells in some species have fibers, evidently cytoskeletal in function. The adhesive tubules are quite similar in all of these species and provide few characters for determining within-group relationships of the gastrotrichs. The duo-gland system of the Gastrotricha is probably not homologous with that of the Turbellaria.Abbreviations Used in Figures cu cuticle - ep epidermal cell - f fiber - la lateral adhesive organ - m muscle - pa posterior adhesive organ - rg releasing gland - sc sensory cilium - scb sensory cell body - vg viscid gland This research was supported by NSF grants DEB-77-06058 (S. Tyler, P.I.) and GB 42211 (R.M. Rieger, P.I.)     

Utility of complete large and small subunit rRNA genes in resolving the phylogeny of the Neodermata (Platyhelminthes): implications and a review of the cercomer theory

We combined nearly complete sequences of large (LSU) and small (SSU) subunit rDNA from 32 flatworm species to estimate the phylogeny of the Platyhelminthes using maximum parsimony, maximum likelihood and Bayesian inference methods. Rooted against the Catenulida, combined evidence trees offered no support for the Revertospermata, which was also rejected by constraint analysis. Generally, nodal support was higher for groupings estimated from the combined data partitions and all methods of analysis provided congruent estimates of phylogeny. The Monogenea and Proseriata were resolved as monophyletic, rejecting previous suggestions of paraphyly based on SSU and partial LSU data sets and thus supporting widely accepted morphological synapomorphies. Monophyly of the Neodermata was supported and its sister group was a clade of neoophoran 'turbellarians' to the exclusion of the Proseriata which in turn was more basal. Taxa with similar spermatology to the Neodermata ( Ichthyophaga , Notentera , Urastoma and Kronborgia ) were the sister group to Tricladida + Prolecithophora, which in turn were sister to the Rhabdocoela. Polycladida + Macrostomida + Lecithoepitheliata was the earliest divergent offshoot of the Rhabditophora. Among the Neodermata, the Cercomeromorphae (Cestoda + Monogenea) was not supported, whereas Cestoda + Trematoda was well supported. Although there is no known synapomorphy for this latter grouping, our data highlight problems associated with the 'cercomer theory' and we reject putative homologies regarding neodermatan 'cercomers' that have been sustained in the literature without careful scrutiny.  © 2003 The Linnean Society of London, Biological Journal of the Linnean Society , 2003, 78, 155–171.     

Comparative ultrastructure of the pharynx simplex in turbellaria

Summary The simple pharynges in thirteen species of Turbellaria in the orders Macrostomida, Haplopharyngida, Catenulida, and Acoela have been studied by electron microscopy. After consideration of the functional aspects of the pharynx simplex, the relationship of the pharynx simplex ultrastructure to the phylogeny of the above mentioned groups is analyzed.The Haplopharyngida and Macrostomida are united as a group by the following characters: a pharynx transition zone of 1–5 circles of insunk cells with modified ciliary rootlets or no cilia, pharynx sensory cells without stereocilia collars and with a variable number of cilia, a prominent nerve ring with more than 30 axons circling the pharynx at the level of the beginning of the pharynx proper distal to the gland ring, 2 or more gland cell types in the pharynx, with at least two layers of muscle present and the longitudinal muscles derived from regular and special body wall circular muscles and a prominent post-oral nerve commissure. This specific arrangement can be distinguished from the other pharynx simplex types and is called the pharynx simplex coronatus.The catenulid pharynx simplex is characterized by the lack of a prominent nerve ring, no prominent post-oral commissure, a transition zone with epidermal type ciliary rootlets, recessed monociliated sensory cells, and one or no type of pharynx gland cell. The Acoela are specialized because of the epidermal type rootlets in the pharynx proper. They also lack a transition zone and a prominent nerve ring and have monociliated sensory cells different from the catenulid type.Ultrastructural characters of the pharynx simplex support the view that the Haplopharyngida-Macrostomida are monophyletic. The more primitive catenulid pharynx probably arose from a common ancestral pool with the Haplopharyngida and Macrostomida, although it does not appear possible presently to establish a clear monophyletic line for these forms. The various pharynx types within the Acoela appear to indicate independent origins with no clear link to the basic pharynx simplex type in the three other orders.Abbreviations Used in Figures a nerve axon - ar accessory rootlet - bb basal body - bn brain-nerve ring commissure - c caudal rootlet - ce centriole - ci cilium - cm circular muscle - cp ciliary pit - cu cuticle - cw cell web - d dictyosome - dp proximal pharynx proper cell - e epidermis - er rough endoplasmic reticulum - f fibrous rod - g gastrodermis - gc gastrodermal gland cell - he heterochromatin - i intercellular matrix - lc lateral nerve cord - lm longitudinal muscle - m mitochondria - mo mouth - mt microtubules - mv microvilli - n nucleus - nr nerve ring - ns neurosecretory granules - p pharynx proper - ph pharynx - po post-oral commissure - r rostral rootlet - rm radial muscle - s sphincter - sc sensory cell - sj septate junction - sr sensory rootlet - t transition zone - u ultrarhabdite - v vertical rootlet - va food vacuole - za zonula adhaerens - 1 type I gland cell - 2 type II gland cell - 3 type III gland cell - 4 type IV gland cell - 5 type V gland cell - 6 type VI gland cell - 7 type VII gland cell     

Turbellarian assemblages in freshwater lagoons in southern Brazil

Turbellarians, which typically feed on bacteria, algae, rotifers, oligochaetes, dipteran larvae, microcrustaceans, and other organisms, are abundant in diverse types of wetlands. Despite their importance, abundance, and species richness in freshwater environments, turbellarians are seldom considered in studies on biodiversity. We analyzed the structure of turbellarian communities in shore areas of three categories of permanent wetlands classified according to their perimeter as small, intermediate, and large during an annual cycle. In total, 1847 turbellarians were collected representing 42 species and 15 genera, from the orders Catenulida, Macrostomida, Lecithoepitheliata, Rhabdocoela, and Tricladida. Sixteen species were common to the three categories of wetlands, whereas nineteen species were unique to a particular category. Species composition varied among wetlands of different sizes; small, intermediate, and large wetlands had different dominant species. We found seasonal differences in community composition over the year, but no significant differences in mean values of observed species richness among wetlands with different sizes and among seasonal samples. The estimated species richness was, however, higher in the small wetlands, followed by the large and intermediate wetlands. In the summer, abundance was significantly lower in the small water bodies than in the intermediate and large bodies of water. Our results reinforce the need for conservation of wetlands of different sizes.     

Comparative characterization of the nervous system of the Turbellaria

Initial stages of the centralization of the nervous apparatus in the Turbellaria can be traced through a comparison of the structure of the nervous system in various representatives of the class. The most primitive state, found in the Acoela, is predominantly plexiform with a varying number of longitudinal trunks. Three, and in some cases four, longitudinal trunks are found in the Proseriata and Temnocephalida. Commissures appear in the Macrostomida and all higher orders and form an orthogon. Brain shape varies from ring-shaped in the Acoela to bilobed in the Neorhabdocoela. While the nervous system of the Polycladida is peculiar, having numerous lateral trunks and separation of dorsal and ventral parts of the nervous system, the development of the nervous system in Müller's larvae of polyclads shows it is of an orthogonal type comparable to other platyhelminths. Transition to parasitism is accompanied by some progressive transformations in the structure of the nervous system.     

Frontal glands and frontal sensory structures in the Macrostomida (Turbellaria)

The ultrastructure of the frontal gland complex of six species of Macrostomida is investigated. In all species it comprises an array of discretely emerging gland necks of at least two gland types, including one with rhammite secretion granules and one with rhahdite granules. Moreover, mucous glands and glands containing other secretion granules are found in Microstomum sp. No intermeditate form which would allow bridging of the present lack of ultrastructural, histochemical and positional similarities between the Macrostomida and the Acoela is found in the examined species. Therefore, the probability of homology between the frontal organs of the Acoela and the frontal glands of the Macrostomida remains low. Even though two or three tyes of sensory receptors are found distributed over the anterior end of all examined species, the frontal gland complex does not appear to be sensory. Because of the uniformity in frontal gland ultrastructure. relationships within the Macrostomida based on this character alone cannot be detected.     

Scanning and Transmission Electron Microscopic Observations on Surface Structures of Three Turbellarian Species

The body surface of Microstomum lineare, Bothriomolus balticus and Archilopsis unipunctata was examined in scanning electron microscope. The threedimensional appearance of adhesive duo-gland organs, receptor cilia, globular bodies and pistil-like projections is described. The adhesive duo-gland papillae of Bothriomolus and Archilopsis appear as bouquetlike structures on either side of the tail as well as on the cilia covered body. In Microstomum the papillae occur as single projections among the ciliary body für. Supplementary TEM investigation revealed crystalline bodies in the cytoplasm of viscid gland cells.     

Ultrastructure of the nerve cells and sensilla of Geocentrophora baltica (Platyhelminthes,Lecithoepitheliata) and the surface sensilla in the Geocentrophora group

Two types of nerve cell could be distinguished ultrastructurally in the central nervous system of Geocentrophora baltica (Prorhynchida, Lecithoepitheliata). Both show invaginations in the plasma membrane, but they differ in the character of the cytoplasm (light or densely stained) and the distribution of the neuronal vesicles (evenly or in groups). Different kinds of vesicles and neuronal release sites are observed. Special features of the synapses are pronounced local thickenings of the presynaptic membrane connected to paramembranous densities. In G. baltica and five endemic Geocentrophora spp. from Lake Baikal six types of surface sensillum were observed at the epidermal surface: 1. those with a long thin rootlet; 2. a short, balloon-shaped cilium with an aberrant axoneme and a reduced rootlet; 3. a rootlet branching into many striated bundles; 4. a thick rootlet; 5. a reduced rootlet and numerous neurotubules;and 6. collared sensilla each with one cilium in a deep pit surrounded by a collar of 11 to 12 microvilli. The variable number of microvilli in the collared sensillum is considered plesiomorphic relative to the stable number of eight microvilli known in sensilla of the Prolecithophora, Proseriata, and Rhabdocoela. The ultrastructure of the collar sensillum indicates that the Lecithoepitheliata is only distantly related to the Prolecithophora and higher turbellarians.     

5S rRNA sequences of 12 species of flatworms: implications for the phylogeny of the Platyhelminthes

5S rRNAs from 12 species of free living and parasitic platyhelminthes were sequenced. In the phylogenetic analysis, attention was focused on the statistical estimates of the trees corresponding to existing phylogenetic hypotheses. The available 5S rRNA data agree well with widely accepted views on the relationships between the Acoela, Polycladida, Tricladida, and Neorhabdocoela; our analysis of the published 18S rRNA sequences also demonstrated good correspondence between these views and molecular data. With available 5S rRNA data the hypothesis that the dalyellioid turbellarians is the sister group of the Neodermata is less convincing than the hypotheses proposing the Neodermata as the sister group of the Neorhabdocoela, or of the Seriata, or of the branch uniting them. A relatively low rate of base replacement in parasitic flatworms, probably, accounts for the uncertain position of the Neodermata, while a relatively high rate in planarians may explain a relatively too early divergence of the Tricladida in several published phylogenetic trees constructed from various rRNA data.     

Hopping locomotion in a nematode: Functional anatomy of the caudal gland apparatus of Theristus caudasaliens sp. n.

The interstitial nematode Theristus caudasaliens n. sp. normally locomotes by hopping on the left side of its tail tip, a mode of locomotion that is unique among nematodes. The animal uses its caudal glands and caudal musculature to perform the hops, attaching itself momentarily between hops with the glands and executing the hops by straightening and curling the posterior part of its body. The caudal gland apparatus can be seen by electron microscopy to consist of five gland cells of two different types. Three of these cells, termed viscid glands, are involved in adhesion of the animal to substrates and produce ovoid granules with a central dense band. The other two cells are characterized by smaller, lessdense granules and presumably function in releasing the animal from substrates. The ducts of both gland types extend to the tail tip where they terminate in a common crescent-shaped space. Their secretions are released to the outside through two pores on the left side of the tail tip. There is no spinneret valve in this nematode. The muscles of the tail and of the mid-body region are developed to the same extent. The caudal gland apparatus can be compared with the duo-gland adhesive organs of other interstitial animals, but its homology with either these organs or the caudal glands of other nematodes is uncertain. Theristus caudasaliens is described as a new species.     

Comparative morphology of statocysts in the Plathelminthes and the Xenoturbellida

The general fine-structural organization of statocysts in Catenulida, Nemertodermatida, Acoela, Proseriata, Lurus (Dalyellioida), and Xenoturbella are summarized. In lithophorous (statocyst-bearing) members of the Catenulida, the statocysts exhibit a few parietal cells and one or several movable statoliths within a spacious intracapsular cavity. Statocysts in the Nemertodermatida have several parietal cells and two lithocytes, each equipped with one statolith, whereas those of the other acoelomorphan taxon, the Acoela, always have two parietal cells and one movable lithocyte. The statocysts of lithophorous members of the Proseriata represent more sophisticated systems: each has two clusters of accessory cells in addition to several parietal cells and a voluminous lithocyte in which the statolith is movable. In catenulids and proseriates, processes of outer neurons penetrate the capsule of the statocyst, whereas such innervations have not been found in the Nemertodermatida and Acoela. I conclude that the different types of statocysts have evolved independently within the Plathelminthes. Xenoturbella displays an intraepidermal statocyst with many monociliary parietal cells and several mobile cells (lithocytes) within the central cavity of the statocyst. Each of these mobile cells carries a statolith-like structure and one prominent cilium. The statocyst of Xenoturbella does not correspond to any type of plathelminth statocyst.     

Ultrastructure of the frontal organ in Convoluta and Macrostomum spp.: significance for models of the turbellarian archetype

Present models of turbellarian evolution depict the organism with a frontal organ — a complex of glands whose necks emerge at the anterior tip of the body — and therefore imply that this organ is homologous throughout the Turbellaria. However, comparisons of representatives of the Acoela and Macrostomida, two putatively primitive orders of the Turbellaria, show that frontal organs in these two are not similar in ultrastructure or histochemistry. The acoel Convoluta pulchra had a prominent cluster of frontal mucous glands whose necks emerged together in a frontal pore at the exact apical pole of the organism, and an array of smaller glands of at least five other types opened at the anterior end, separately from and ventral to this pore. The frontal organs (Stirndrüsen) of two species of Macrostomum on the other hand, comprised an array of discretely emerging necks of at least two gland types including one with rhabdiform (rhammite) and one with globular mucous secretion granules neither of which emerge at the apical pole. In neither species did the organ appear to be sensory. Our findings indicate a low probability of homology between the frontal glands of the Acoela and Macrostomida.     

Structure and evolution of the pharynx simplex in acoel flatworms (Acoela)

The homology of pharynges within the mostly pharynx‐less Acoela has been a matter of discussion for decades and even the basic question of whether a pharynx is a primitive trait within the Acoela and homologous to the pharynx of platyhelminth turbellarians is open. By using fluorescence staining of musculature, as well as conventional histological techniques and transmission electron microscopy, the present study sets focus on the mouth and pharynx (where present) of seven species of Acoela within Paratomellidae, Solenofilomorphidae, Hofsteniidae, Proporidae, and Convolutidae, as well as one species of Nemertodermatida and Catenulida, respectively. It is shown that among the investigated families of acoels there is a great variability in muscle systems associated with the mouth and pharynx and that pharynx histology and ultrastructural characters are widely diverse. There are no close similarities between the acoel pharynges and the catenulid pharynx but there is a general resemblance of the musculature associated with the mouth in the representatives of Paratomellidae and Nemertodermatida. On the basis of the profound differences in pharynx morphology, three major conclusions are drawn: 1) the pharynges as present in Recent acoels are not homologous to the pharynx simplex characteristic for Catenulida and Macrostomida within the Platyhelminthes; 2) the different muscular pharynx types of acoels are not homologous between higher taxa and thus a single acoel‐type pharynx simplex cannot be defined; 3) the presence of a muscular pharynx most likely does not represent the ancestral state. J. Morphol, 2009. © 2008 Wiley‐Liss, Inc.     

Frontal organs in the Acoelomorpha (Turbellaria): Ultrastructure and phylogenetic significance

Using characters discernible through electron microscopy, we redefine the organ traditionally identified as the frontal organ in acoelomorph turbellarians as being a collection of two to several large mucus-secreting glands whose necks emerge together through a frontal pore at the exact apical pole of the body, i.e. at the point where the pattern of epidermal ciliary rootlets converges. Representatives that we have studied of each of the acoel families Paratomellidae, Diopisthoporidae, Solenofilomorphidae, Convolutidae, Otocelidae, and Mecynostomidae, as well as a representative of the Nemertodermatida, have such glands. Up to five additional types of glands that open anteriorly outside of the frontal pore, some of which are indistinguishable from glands of the general body wall, could be seen in the nemertodermatid, in Hesiolicium inops (Paratomellidae), and in representatives of the latter four acoel families. In Paratomella, three different types of glands open in diffuse fashion in a frontal glandular complex reminiscent of that in the Macrostomida.Sensory elements near the frontal pore appear to be independent of the gland necks, and so the organ cannot be considered a sensory organ.The frontal organ, as described above, appears very likely to be homologous within the Acoelomorpha, and represents another strong (although unrooted) autapomorphy for this line of turbellarian evolution.     

Notes on the biology of some psammophile Turbellaria of the Black Sea

The biology of two marine turbellarians, Cercyra hastata (Tricladida) and Pseudomonocelis ophiocephala (Proseriata) has been studied over a period of five years. They are the main components of the biocoenosis of the saccocirrus sand of Sevastopol Bay. These species have a significant role in the processes of secondary production and transformation of the organic matter in the coastal zone.     

FMRFamide- and neurotensin-immunoreactive elements in the intestine of some polyclad and triclad flatworms (Turbellaria)

By means of immunohistochemistry with antisera to tetrapeptide FMRFamide and regulatory peptides neurotensin and calcitonin intestines of marine turbellarians Notoplana atomata, N. humilis (Polycladida) and Procerodes littoralis (Tricladida) were investigated. In all flatworms polymorphous cells and processes reacting with antibodies to FMRFamide and neurotensin but not with calcitonin were revealed. These cell elements are localized both in the epithelium and beneath it. FMRFamide-immunoreactive cells and processes of investigated turbellarians and neurotensin-immunoreactive elements in P. littoralis obviously belong to the nervous system, while intraepithelial neurotensin-immunoreactive cells of polyclads share some morphological features with endocrine-like cells.     

Ultrastructural features of oogenesis in some marine neoophoran turbellarians

An ultrastructural study of oogenesis has been undertaken in some marine species of neoophoran turbellarians belonging to the Tricladida, Proseriata, and Prolecithophora. Among marine triclads, Cercyra hastata has oocytes with a remarkable amount of what appears to be autosynthetic proteinaceous yolk, while Procerodes dohrni and P. lobata have alecithal oocytes. Among the Proseriata, several species of the primitive family Monocelididae (subfamily Monocelidinae) have oocytes with a discrete amount of what appears to be autosynthetic yolk, while Parotoplana macrostyla, of the derived family Otoplanidae, has alecithal eggs. Finally preliminary observations on Plagiostomum maculatum (order Prolecithophora) suggest that oocytes have autosynthetic yolk globules.These results support the hypothesis (previously formulated on the basis of similar ultrastructural investigations on freshwater triclads) that the presence of autosynthetic yolk in some neoophoran turbellarians can be interpreted as a primitive character inherited from an ancestor with archoophoran organization. This plesiomorphic character would still be maintained in some species while lost in others following differentiation of vitellaria which are characteristic of the Neoophora.     

The phylogenetic significance of sperm morphology in the Platyhelminthes

The phylogenetic significance of flatworm sperm morphology is discussed against the background of general spermatology. The modified type of spermatozoon of the Nemertodermatida, a group of primitive flatworms, indicates that the Platyhelminthes evolved from forms characterized by the primitive type of metazoan sperm and by the primitive mode of fertilization, implying the release of sperm freely into sea water.The occurrence of aberrant types of spermatozoa in most platyhelminths is obviously a consequence of early evolution of the internal mode of fertilization, which characterizes all true members of this group. It can be concluded, from the ultrastructure of these aberrant spermatozoa that higher metazoans cannot have evolved from seriated flatworms related to the recent Seriata (Proseriata and Tricladida). Even the seemingly primitive Acoela have such aberrant spermatozoa that evolution of higher metazoans from acoels related to the recent Acoela seems highly improbable.The ultrastructure of the spermatozoa of the parasitic groups of flatworms (Monogenea, Digenea, Cestoda) is very similar to that found in the Kalyptorhynchia, a further indication that the parasitic groups are related to the rhabdocoel turbellarians.