Sweet or salty? The origin of freshwater gastrotrichs (Gastrotricha,Chaetonotida) revealed by molecular phylogenetic analysis

Chaetonotidae is the most diverse and widely distributed family of the order Chaetonotida (Gastrotricha) and includes both marine and freshwater species. Although the family is regarded as a sister taxon to the exclusively marine Xenotrichulidae, the type of environment, marine or freshwater, where Chaetonotidae originated is still not known. Here, we reconstructed the phylogeny of the family based on molecular sequence data and mapped both morphological and ecological characters to determine the ancestral environment of the first members of the family. Our results revealed that the freshwater genus Bifidochaetus is the earliest branching lineage in the paraphyletic Chaetonotidae (encompassing Dasydytidae and Neogosseidae). Moreover, we reconstructed Lepidochaetus-Cephalionotus clade as a monophyletic sister group to the remaining chaetonotids, which supports Kisielewski's morphological based hypothesis concerning undifferentiated type of body scales as a most primary character in Chaetonotidae. We also found that reversals to marine habitats occurred independently in different Chaetonotidae lineages, thus marine species in the genera Heterolepidoderma, Halichaetonotus, Aspidiophorus and subgenera Chaetonotus (Schizochaetonotus) or Chaetonotus (Marinochaetus) should be assumed as having secondarily invaded the marine environment. Character mapping revealed a series of synapomorphies that define the clade that includes Chaetonotidae (with Dasydytidae and Neogosseidae), the most important of which may be those linked to reproduction.     

Phylogeny of Chaetonotidae and other Paucitubulatina (Gastrotricha: Chaetonotida) and the colonization of aquatic ecosystems

Kånneby, T., Todaro, M. A., Jondelius, U. (2012). Phylogeny of Chaetonotidae and other Paucitubulatina (Gastrotricha: Chaetonotida) and the colonization of aquatic ecosystems. —Zoologica Scripta, 42, 88–105. Chaetonotidae is the largest family within Gastrotricha with almost 400 nominal species represented in both freshwater and marine habitats. The group is probably non‐monophyletic and suffers from a troubled taxonomy. Current classification is to a great extent based on shape and distribution of cuticular structures, characters that are highly variable. We present the most densely sampled molecular study so far where 17 of the 31 genera belonging to Chaetonotida are represented. Bayesian and maximum likelihood approaches based on 18S rDNA, 28S rDNA and COI mtDNA are used to reconstruct relationships within Chaetonotidae. The use of cuticular structures for supra‐specific classification within the group is evaluated and the question of dispersal between marine and freshwater habitats is addressed. Moreover, the subgeneric classification of Chaetonotus is tested in a phylogenetic context. Our results show high support for a clade containing Dasydytidae nested within Chaetonotidae. Within this clade, only three genera are monophyletic following current classification. Genera containing both marine and freshwater species never form monophyletic clades and group with other species according to habitat. Marine members of Aspidiophorus appear to be the sister group of all other Chaetonotidae and Dasydytidae, indicating a marine origin of the clade. Halichaetonotus and marine Heterolepidoderma form a monophyletic group in a sister group relationship to freshwater species, pointing towards a secondary invasion of marine environments of these taxa. Our study highlights the problems of current classification based on cuticular structures, characters that show homoplasy for deeper relationships.     

The musculature of Draculiciteria tessalata (Chaetonotida, Paucitubulatina): implications for the evolution of dorsoventral muscles in Gastrotricha

The muscular system of the marine interstitial gastrotrich Draculiciteria tessalata (Chaetonotida, Paucitubulatina) was analyzed with fluorescent phalloidin. Muscles in circular, longitudinal, helicoidal and dorsoventral orientations were found. Circular muscles were present as discreet rings on the pharynx only. Five pairs of longitudinal muscles were found in dorsal, lateral and ventral positions. One of the two pairs of lateral muscles is newly described for the species. Helicoidal muscles, external to the circular muscles and some longitudinal bands, spiraled around the pharynx and anterior portion of the intestine. Two pairs of segmentally-arranged dorsoventral muscles were also present. Lateral dorsoventral muscles extended from the base of the pharynx to the anterior part of the caudal furca. Medial dorsoventral muscles extended from the pharyngeal-intestinal junction into each ramus of the caudal furca. A hypothesis on the evolution of dorsoventral muscles in D. tessalata is proposed which includes a splitting of circular muscles into separate somatic and splanchnic components with a further displacement of both muscle sets into a dorsoventral orientation.     

The muscular system of Musellifer delamarei (Renaud-Mornant, 1968) and other chaetonotidans with implications for the phylogeny and systematization of the Paucitubulatina (Gastrotricha)

We studied comparatively the muscle organization of several gastrotrich species, aiming at shedding some light on the evolutionary relationships among the taxa of the suborder Paucitubulatina. Under confocal laser scanning microscope, the circular muscles were present in the splanchnic position as incomplete circular rings in Musellifer delamarei (Chaetonotidae) and Xenotrichula intermedia (Xenotrichulidae) and as dorsoventral bands in Xenotrichula punctata, Heteroxenotrichula squamosa and Draculiciteria tesselata (Xenotrichulidae); in the somatic position, M. delamarei shares the presence of dorsoventral muscles with all the Xenotrichulidae, in contrast with the remaining Chaetonotidae that lack these muscles. Maximum parsimony analysis of the muscular characters confirmed monophyly of Paucitubulatina and Xenotrichulidae, while the Chaetonotidae was paraphyletic, with the exclusion of Musellifer , which is the most basal genus within the Paucitubulatina. Xenotrichulidae is the sister taxon to Chaetonotidae, which in turn has Polymerurus as the most basal taxon. In general, the results agree with recent phylogenetic inferences based on molecular characters and support the hypothesis that, within Paucitubulatina, dorsoventral muscles are plesiomorphies retained in marine, interstitial, hermaphroditic gastrotrichs. Dorsoventral muscles were subsequently lost during changes in lifestyle and reproduction modality that took place with the invasion of the freshwater environment. This new information prompted us to reconsider the systematization of Chaetonotidae, proposing the establishment of Muselliferidae fam. nov. to include the genera Musellifer and Diuronotus .  © 2008 The Linnean Society of London, Biological Journal of the Linnean Society , 2008, 94 , 379–398.     

Comparative myoanatomy of cycliophoran life cycle stages

The metazoan phylum Cycliophora includes small cryptic epibionts that live attached to the mouthparts of clawed lobsters. The life cycle is complex, with alternating sexual and asexual generations, and involves several sessile and free‐living stages. So far, the morphological and genetic characterization of cycliophorans has been unable to clarify the phylogenetic position of the phylum. In this study, we add new details on the muscular anatomy of the feeding stage, the attached Prometheus larva, the dwarf male, and the female of one of the two hitherto described species, Symbion pandora. The musculature of the feeding stage is composed of myofibers that run longitudinally in the buccal funnel (two fibers) and in the trunk (variable number of fibers). The mouth opening is lined by a myoepithelial ring musculature. A complex myoepithelial sphincter is situated proximal to the anus. In the attached Prometheus larva, three longitudinal sets of myofilaments run dorsally, laterally, and ventrally along the entire anterior‐posterior body axis. The muscular architecture of the dwarf male is complex, especially close to the penis, in the posterior part of the body. An X‐shaped muscle structure is found on the dorsal side, whereas on the ventral side, longitudinal muscles and a V‐shaped muscle structure are present. These muscles are complemented by additional dorsoventral muscles. The mesodermal muscle fibers attach to the cuticle via the epidermis in all life cycle stages studied herein. The musculature of the female is similar to that of the Pandora larva of Symbion americanus and includes dorsoventral muscles and longitudinal muscles that run in the dorsal and ventral body region. Overall, our results reveal striking similarities in the muscular arrangement of the life cycle stages of both Symbion species. J. Morphol., 2010. © 2009 Wiley‐Liss, Inc.     

Ultrastructural observations of the protonephridia of Polymerurus nodicaudus (Gastrotricha: Paucitubulatina)

Kieneke, A. and Hochberg, R. 2012. Ultrastructural observations of the protonephridia of Polymerurus nodicaudus (Gastrotricha: Paucitubulatina). —Acta Zoologica (Stockholm) 93 : 115–124. We studied different regions of the protonephridia of the limnic gastrotrich Polymerurus nodicaudus by means of light and electron microscopy to determine how freshwater species might differ from their marine relatives. Microscopic and ultrastructural characters are in accordance with another limnic species of Paucitubulatina, Chaetonotus maximus, whose protonephridial system has been previously reconstructed. Shared protonephridial characters of both species include the presence of highly elongate terminal organ cilia, microvilli, and the canal cell lumen as well as the presence of a conspicuous anterior loop of the protonephridial lumen. These features are not present in representatives of earlier, marine, paucitubulatan lineages (i.e., Xenotrichulidae) and so are assessed as evolutionary novelties that were likely important for the successful colonization of the freshwater environment.     

Musculature in polychaetes: comparison of Myrianida prolifera (Syllidae) and Sphaerodoropsis sp. (Sphaerodoridae)

Abstract. The relationship of the polychaete taxa Syllidae and Sphaerodoridae within Phyllodocida is still unresolved: phylogenetic analyses either show them as sister groups or more widely separated. The present article aims to provide information about the structure of the muscular system that could be essential for understanding their relationship. A crucial point is whether the body wall contains circular muscles, which has recently been shown to be absent in more taxa than previously known. The F-actin filaments in members of Myrianida prolifera (Syllidae) and Sphaerodoropsis sp. (Sphaerodoridae) were labeled with phalloidin and their three-dimensional relationships reconstructed by means of confocal laser scanning microscopy. Among the noteworthy differences that emerged between the species are (1) members of M. prolifera possess four, those of Sphaerodoropsis sp. eight, longitudinal muscle strands; (2) the body wall in M. prolifera contains transverse fibers in a typical, supralongitudinal position, while in Sphaerodoropsis sp., corresponding fibers lie beneath the longitudinal strands; (3) pro- and peristomium in M. prolifera have no distinct F-actin fibers, while five longitudinal pairs and three single transverse muscular fibers shape the anterior end in Sphaerodoropsis sp.; (4) the proventricle of M. prolifera comprises primarily radial muscle fibers arranged in distinct rows, while in Sphaerodoropsis sp. the axial proboscis consists of longitudinal and circular fibers and radial fibers are lacking; (5) in M. prolifera, the proximal and distal sections of the two anteriormost pairs of dorsal cirri possess longitudinal myofilaments, which are separate from the body wall musculature; by contrast, all appendages in Sphaerodoropsis sp. do not; (6) both species have bracing muscles: in M. prolifera they are positioned above the longitudinal fibers, whereas in Sphaerodoropsis sp. they are uniquely positioned between longitudinal and sublongitudinal transverse fibers. These results do not support a sister-group relationship of Syllidae and Sphaerodoridae. In addition, Sphaerodoropsis sp. is yet another example in the list of polychaetes lacking typical circular muscles in the body wall.     

The muscular system of Dactylopodola baltica and other macrodasyidan gastrotrichs in a functional and phylogenetic perspective

The gastrotrich muscular system is characterized by band-like muscles arranged in orientations that reflect both function and phylogeny. To better understand the evolution of the Dactylopodolidae, a putative primitive lineage and potential sister group to other extant macrodasyidans, we have used a fluorescent phalloidin stain to visualize muscle patterns in the marine gastrotrich Dactylopodola baltica and eight other species of Macrodasyida from four families. The musculature of D. baltica is arranged as a series of circular, helicoidal and longitudinal bands around the digestive tract. Circular muscles and longitudinal muscles were found in splanchnic and somatic positions. Helicoidal muscles, in 50–60° angles with respect to the longitudinal body axis, surrounded circular and longitudinal splanchnic muscles in a spiralling orientation. The largest longitudinal muscles were the ventrolateral bands composed of numerous cross-striated myocytes arranged in parallel arrays. The overall arrangement of the muscular system of D. baltica showed several similarities to other macrodasyidan gastrotrichs, including the presence and location of circular, helicoidal and longitudinal muscles, their orientation with respect to the longitudinal body axis and their points of insertion. Unique to D. baltica is the anterior and posterior arrangement of the ventrolateral muscles and the orientation of muscle branches that supply the ventral and dorsal aspects of the pharynx. Muscle data from observations of D. baltica and eight additional species were coded as phylogenetic characters, mapped onto a cladogram and compared to an existing phylogeny of the order. The direction of evolutionary change in specific muscle groups was inferred, as was the ground pattern of muscles for the Macrodasyida.     

A phylogenetic approach to species delimitation in freshwater Gastrotricha from Sweden

Gastrotricha is a cosmopolitan group of aquatic invertebrates. To date, approximately 765 species have been described. This study is the first to deal with species delimitation and cryptic species of freshwater Gastrotricha. Three commonly encountered species, Heterolepidoderma ocellatum, Lepidochaetus zelinkai, and Lepidodermella squamata, are investigated for cryptic speciation. Most of the material is based on Swedish specimens but closely related species from other parts of the world are also included. Taxonomic revisions are supported by phylogenies based on 18S rRNA, 28S rRNA, and COI mtDNA of freshwater Chaetonotidae from several genera and inferred from Bayesian and maximum likelihood approaches. Heterolepidoderma ocellatum f. sphagnophilum is raised to species level, under the name H. acidophilum n. sp. Moreover, genetic data based on COI indicate large variation between two morphologically very similar groups of Lepidodermella squamata. The extent of cryptic speciation in L. zelinkai appears low. Based on the phylogenetic hypothesis presented in this article, the new species, Lepidodermella intermedia n. sp., from northern Sweden is also described. The phylogenetic hypothesis generated shows that Chaetonotidae is a non-monophyletic group.     

Nordadriatische Gastrotrichen

Zusammenfassung 1. 22 neue und 8 bereits bekannte Gastrotrichen-Arten werden beschrieben, die — mittels MgCl₂-Extraktion gewonnen — eulitoralen und sublitoralen Sandböden der nördlichen Adria entstammen und mit Phasenkontrast-Optik lebend untersucht wurden.2. Von den neuen Arten sind 7 den Macrodasyoidea und 15 den Chaetonotoidea zuzurechnen.3.Macrodasys caudatus besitzt 4 verschiedene Bursa-Typen, die regelmäßig mit einer bestimmten Anzahl reifer und unreifer Eier korreliert sind.4. 2 neueTetranchyroderma-Arten zeigen eine auf schmale Streifen beschränkte Vierhaker-Bedeckung; an einer weiteren Art dieser Gattung sind die Vierhaker auf kleine laterale Felder in der Pharynxregion reduziert.5. An Hand 4 neuerChaetonotus-Arten aus derschultzei-Gruppe wird das die Gruppe gegenüber anderen Arten der Gattung heraushebende Merkmal diskutiert: der dreikantige dorsale Schuppenstachel, dessen mediane, dem Körper abgewandte Kante immer nur in eine Spitze ausgezogen ist.6. Die UntergattungHalichaetonotus wird ausChaetonotus herausgehoben und erhält den Rang einer selbständigen Gattung, deren bindendes Merkmal das gemeinsame Auftreten dorsaler Kielschuppen und ventrolateraler Stacheln, Stachel- oder Lamellenschuppen ist.7. Im Zusammenhang mit 4 neuenHeterolepidoderma-Arten werden die Merkmale dieser Gattung einer Diskussion unterworfen; Arten, die ausschließlich gekielte Schuppen oder auch Kiele ohne deutlich erkennbare Basisschuppen tragen, sind vorläufig auch dann zuHeterolepidoderma zu stellen, wenn diese Elemente nur wenige Längsreihen bilden.8.Aspidiophorus mediterraneus variiert stark vor allem in Körpergröße, Zahl und Form der Stielschuppen.

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North Adriatic gastrotrichs

Twentytwo new and 8 known species of gastrotrichs are described from eulittoral and sublittoral sandy bottoms of the northern Adriatic Sea. The MgCl₂ method was used for extraction from the substrate. Only living material was studied employing phase contrast microscopy. Seven of the new species belong to the order Macrodasyoidea, 15 are members of the order Chaetonotoidea. InMacrodasys caudatus, 4 different types of bursae copulatrices were found to be usually correlated with a specific number of mature and immature eggs. In 2 new species ofTetranchyroderma, the four-pronged hooks are restricted to narrow bands; another species of that genus has four-pronged hooks only in the pharyngeal region being reduced to small lateral patches. Four new species ofChaetonotus belong to theschultzei group; the diagnostic feature of this group is the tri-cornered spine whose distal edge is more oblique and extends always in only one fine tip.Halichaetonotus is given the rank of a genus distinct fromChaetonotus; the diagnostic feature ofHalichaetonotus species is the dorsal occurrence of both keeled scales and of spines, as well as the ventrolateral spined scales or foliaceous scales. Four new species ofHeterolepidoderma lead to the discussion of the characters of the genus. Species belong toHeterolepidoderma if they are covered by keeled scales only or by keels lacking a distinct base scale. The number of longitudinal rows composed by these cuticular elements is, at the present, of no value to the diagnosis of the genus.

     

Motor supply of the dorsal longitudinal muscles II: Comparison of motoneurone sets in Tracheata

The set of motoneurones (MNs) supplying a specific ensemble of dorsal longitudinal muscles was studied in several segments of a primarily apterygote insect, Lepisma saccharina (Zygentoma), and a centipede, Lithobius forficatus (Chilopoda). In all preparations, a distribution of the MNs in two adjacent ganglia is observed. The cell number and their morphology in the thorax of L. saccharina are similar to the equivalent neural system of two Caelifera species, whereas in the L. saccharina abdomen there is some reduction in cell number. It appears that for both dicondylean insect groups homologous MNs exist. For L. forficatus, 12 MNs are present in the anterior ganglion and 4 in the posterior one. The morphology of these neurones is different compared to the insect MNs supplying an apparently equivalent set of muscles. Additionally, the neural supply of the intersegmental dorsoventral muscle was studied in Schistocerca gregaria, L. saccharina and L. forficatus. Both insect species show a pronounced similarity of the MN set. Again, the neural set in L. forficatus is different from that of the Dicondylia. Our results support the idea that the structure of MNs in the largest present taxon of Insecta, the Dicondylia, is conserved irrespective of crucial changes in the periphery (e.g. primarily apterygote vs oterygote). The muscles and their neurones are probably part of a basic neuromuscular ground pattern. The pronounced differences in a centipede are discussed in phylogenetic terms.Abbreviations DLM dorsal longitudinal muscle - DUM dorsal unpaired median - ISM intersegmental dorsoventral muscle - MN motoneurone - M muscle (number) - N nerve (number)     

Myogenesis in two polyclad platyhelminths with indirect development,Pseudoceros canadensis and Stylostomum sanjuania

SUMMARY Myogenesis of two representatives of Platyhelminthes, Stylostomum sanjuania and Pseudoceros canadensis, was followed from egg deposition until well‐differentiated free‐swimming larval stages, using F‐actin staining and confocal laserscanning microscopy. Zonulae adhaerentes are the only structures to stain before 50% of development between egg deposition and hatching in S. sanjuania, and before 67% of development in P. canadenis. Subsequently, irregular fibers appear in the embryo, followed by a helicoid muscle close to the apical pole. Three longitudinal muscle pairs form, of which the dorsal pair remains more pronounced than the others. Gradually, new muscles form by branching or from double‐stranded muscle zones adjacent to existing muscles. This results in an elaborate muscular bodywall that consists of a single helicoid muscle as well as multiple circular and longitudinal muscles. Diverse retractor muscles insert at the sphincter muscles around the stomodeum. The overall arrangement and formation mode of the larval musculature appears very similar in both species, although only P. canadensis has a primary circular muscle posterior to the helicoid muscle. Muscle formation in the apical region of the embryo precedes that at the abapical pole and the primary longitudinal muscles form slightly later than the primary circular muscles. Myogenesis and larval myoanatomy appears highly conserved among polyclad flatworms, but differs significantly from that of other trochozoan clades. Our data suggest that the larval muscular ground pattern of polyclad larvae comprises a bodywall consisting of a helicoid muscle, circular and longitudinal muscles, several retractor muscles, and sphincter muscles around the stomodeum.     

Body wall muscles in the haplotaxidsHaplotaxis gordioides andPelodrilus leruthi (Annelida,Oligochaeta)

Summary The muscle organization of the body wall in two species of Haplotaxida is described.Haplotaxis gordioides andPelodrilus leruthi show significant differences in the longitudinal muscle layer. The observations suggest that inH. gordioides, the muscle fibres could foreshadow the flat circomyarian organization of microdrile muscles, while theP. leruthi organization recalls the pinnate arrangement of megadrile body wall.     

CLSM analysis of the phalloidin-stained muscle system in Nerilla antennata, Nerillidium sp. and Trochonerilla mobilis (Polychaeta; Nerillidae)

The entire muscle system of Nerilla antennata, Nerillidium sp. and Trochonerilla mobilis was three-dimensionally reconstructed from whole mounts. In juvenile and adult specimens the F-actin musculature subset was stained with FITC-conjugated phalloidin and visualized with a confocal laser scanning microscope (cLSM). The muscle system shows the following major organization: 1) circular muscles are totally absent in the body wall; 2) the longitudinal muscles are confined in two ventral and two dorsal thick bundles; 3) additional longitudinal muscles are located in the ventro- and dorsomedian axis; 4) three segmental pairs of ventral oblique muscles elongate into the periphery: the main dorsoventral muscles that run along the body side posterior and dorsally and the anterior and posterior oblique parapodial muscles, which contribute to the ventral chaetal sacs; 5) one segmental pair of dorsal oblique parapodial muscles, contributing to the dorsal chaetal sacs; 6) five to seven small dorsoventral muscles per segment; and 7) complex head and pharyngeal musculature. These results support the belief that absence of circular muscles in the polychaete body wall is much more widely distributed than is currently presumed.     

The adult musculature of two pseudostomid species reveals unique patterns for flatworms (Platyhelminthes,Prolecithophora)

We analyzed the adult musculature of two prolecithophoran species, Cylindrostoma monotrochum (von Graff, 1882) and Monoophorum striatum (von Graff, 1878) using a phalloidin-rhodamine technique. As in all rhabdithophoran flatworms, the body-wall musculature consisted of three muscle layers: on the outer side was a layer of circular muscle fibers and on the inner side was a layer of longitudinal muscle fibers; between them were two different types of diagonally orientated fibers, which is unusual for flatworms. The musculature of the pharynx consisted of a basket-shaped grid of thin longitudinal and circular fibers. Thick anchoring muscle fibers forming a petal-like shape connected the proximal parts of the pharynx with the body-wall musculature. Male genital organs consisted of paired seminal vesicles, a granular vesicle, and an invaginated penis. Peculiar ring-shaped muscles were only found in M. striatum, predominantly in the anterior body part. In the same species, seminal vesicles and penis only had circular musculature, while in C. monotrochum also longitudinal musculature was found in these organs. Female genital organs were only present in M. striatum, where we characterized a vagina interna, and a bursa seminalis. Transverse, crossover, and dorsoventral muscle fibers were lacking in the middle of the body and greatly varied in number and position in both species.     

Reconstruction of the muscle system in Antygomonas sp. (Kinorhyncha,Cyclorhagida) by means of phalloidin labeling and cLSM

In the present investigation the entire muscle system of the cyclorhagid kinorhynch Antygomonas sp. was three-dimensionally reconstructed from whole mounts by means of FITC-phalloidin labeling and confocal scanning microscopy. With this technique, which proved to be especially useful for microscopically small species, we wanted to reinvestigate and supplement the findings obtained by histological and electron microscopical methods. The organization of the major muscle systems can be summarized as follows: 1) All muscle fibers, apart from the intestinal ones, the spine, and the mouth cone muscles, show a cross-striated pattern; 2) Dorsal longitudinal muscle fibers as well as segmentally arranged dorsoventral fibers occur from segment III to XIII; 3) Diagonal muscle fibers are located laterally in segments III to X; 4) Two rings of circular fibers are present in segment II, forming the closing apparatus in Cyclorhagida. Further circular muscles are present in segment I, forming the mouth cone and the eversible introvert, and in the pharyngeal bulb.     

Three‐dimensional reconstruction of the musculature of various life cycle stages of the cycliophoran Symbion americanus

Cycliophora is a very recently described phylum of acoelomate metazoans with a complex life cycle and a phylogenetic position that has been under debate ever since its discovery in 1995. Symbion americanus, which lives attached to the mouthparts of the American lobster, Homarus americanus, represents the second species described for the phylum. Aiming to increase the morphological knowledge about this cryptic clade, the present study describes the muscle arrangement of the feeding stage, the attached Prometheus larva with the dwarf male inside, the free living male, the Pandora larva, and the chordoid larva of S. americanus using actin staining and confocal laser scanning microscopy. 3D reconstructions of the muscular systems are presented. In the feeding stage, circular muscles compose the buccal funnel aperture. In addition, a pair of muscles runs longitudinally in the buccal funnel. A complex sphincter was found just proximally to the anus, and six longitudinal muscles run from the trunk constriction (“neck”) in basal direction. The musculature of the larval stages and the dwarf male is very complex and includes longitudinal muscles that run dorsally and ventrally. In addition, we found dorso‐ventral muscles. The male has a complex posterior muscle apparatus in the vicinity of the penis. In this stage, X‐ and V‐shaped structures were identified on the dorsal and the ventral side, respectively. Pandora and chordoid larvae possess additional circular muscles. We discuss our findings with respect to muscle elements of other metazoan groups and the chordoid larva of Symbion pandora. J. Morphol., 2009. © 2008 Wiley‐Liss, Inc.     

Morphological variation of hypaxial musculature in salamanders (Lissamphibia: Caudata)

Despite the acknowledged importance of the locomotory and respiratory functions associated with hypaxial musculature in salamanders, variation in gross morphology of this musculature has not been documented or evaluated within a phylogenetic or ecological context. In this study, we characterize and quantify the morphological variation of lateral hypaxial muscles using phylogenetically and ecologically diverse salamander species from eight families: Ambystomatidae (Ambystoma tigrinum), Amphiumidae (Amphiuma tridactylum), Cryptobranchidae (Cryptobranchus alleganiensis), Dicamptodontidae (Dicamptodon sp.), Plethodontidae (Gyrinophilus porphyriticus), Proteidae (Necturus maculosus), Salamandridae (Pachytriton sp.), and Sirenidae (Siren lacertina). For the lateral hypaxial musculature, we document 1) the presence or absence of muscle layers, 2) the muscle fiber angles of layers at mid‐trunk, and 3) the relative dorsoventral positions and cross‐sectional areas of muscle layers. Combinations of two, three, or four layers are observed. However, all species retain at least two layers with opposing fiber angles. The number of layers and the presence or absence of layers vary within species (Necturus maculosus and Siren lacertina), within genera (e.g., Triturus), and within families. No phylogenetic pattern in the number of layers can be detected with a family‐level phylogeny. Fiber angle variation of hypaxial muscles is considerable: fiber angles of the M. obliquus externus range from 20–80°; M. obliquus internus, 14–34°; M. transversus abdominis, 58–80° (acute angles measured relative to the horizontal septum). Hypaxial musculature comprises 17–37% of total trunk cross‐sectional area. Aquatic salamanders show relatively larger total cross‐sectional hypaxial area than salamanders that are primarily terrestrial. J. Morphol. 241:153–164, 1999. © 1999 Wiley‐Liss, Inc.     

Body wall organization in enchytraeids

The muscle organization of the body wall in some species of oligochaetes belonging to the Enchytraeus genus is described. No differences have been detected in their circular muscles, whereas longitudinal muscles show significant differences, allowing an easy identification of the various worm species. In particular, differences are noticeable in the external longitudinal layer. These observations suggest that structural and ultrastructural muscle fiber organizations can be used as a taxonomic tool.