Morphology and ultrastructure of the anterior end of Diplocirrus longisetosus Marenzeller, 1890 (Flabelligeridae, Polychaeta, Annelida)

The morphology and ultrastructure of the sedentary polychaete Diplocirrus longisetosus Marenzeller, 1890, collected from the White Sea, were studied using dissection, histological methods, light microscopy, and both scanning and transmission electron microscopy. The prostomium and peristomium carry a pair of palps, eight branchiae, a pair of nuchal organs and two nephridiopores, ciliated folds and the mouth. The prostomium, peristomium and the first chaetigerous segment with all appendages comprise the so-called siphon complex. The mouth leads to a pharyngeal organ that is closed ventrally and composed of a ventral muscle bulb adjoined dorsally by two folds projecting into the pharyngeal lumen. These parts are connected and enveloped by the longitudinal investing muscle. No tongue-like organ is present. The nervous system of the siphonal part comprises the brain, the circum-oesophageal connectives and the ganglia of the peristomium and first chaetigerous segment.     

Phylogenetic affinities of the Flabelligeridae (Annelida, Polychaeta)

Cirratuliformia includes Acrocirridae, Cirratulidae, Ctenodrilidae, Flabelligeridae, Flotidae and Sternaspidae. The phylogenetic affinities have not been settled due to a limited availability of type or non-type material and the relationship between acrocirrids and flabelligerids have been problematical. In our study, the type material of all type species for all flabelligerid, and most acrocirrid genera have been studied and the morphological features have been used in a phylogenetic analysis. The results indicate that Acrocirridae, Ctenodrilidae, Fauveliopsidae, Flabelligeridae and Flotidae are monophyletic and that Sternaspidae falls within Cirratulidae; however, the latter conclusion might be reversed through increased taxon-sampling. The flabelligerid genera Brada, Flabelligera, Pherusa and Stylarioides each consists of several monophyletic groups and may be split. Conversely, Bradiella includes Diversibranchius, and the pelagic Buskiella includes Flota. The generic affinities of Poeobius remain uncertain, collecting better materials may resolve this issue.     

Revision of Pseudonereis (Polychaeta, Nereididae)

A taxonomic revision of Pseudonereis (Polychaeta, Nereididae) shows that some of the described taxa are very similar in most morphological characteristics. The revision includes all ten taxa considered valid, and are redescribed from type material. Lectotypes are designated for Pseudonereis anomala Gravier, 1901, Pseudonereis noodti (Hartmann-Schröder, 1962) and Pseudonereis trimaculata Horst, 1924. The widely geographically distributed and well-known P. gallapagensis Kinberg, 1865 and P. variegata ( Grube, 1857 ) show striking morphological resemblance to less well-known taxa with similar distribution. Paragnath variation in populations of P. anomala is discussed relating to its geographical distribution. Pseudonereis trimaculata is recorded from Australia for the first time. Taxa belonging to Pseudonereis are predominantly tropical and subtropical. A cladistic analysis using parsimony is included to test for monophyly of Pseudonereis . A monophyletic clade including all Pseudonereis taxa is given low bootstrap support. This clade is supported by the synapomorphies: presence of paragnaths in closely spaced comb-like rows on the maxillary ring on the pharynx, and presence of p-bar paragnaths in Areas II–IV and VII–VIII. Several of the included taxa share the shield-shaped paragnath in Area VI, which serves to distinguish Pseudonereis spp. from Perinereis spp. Paragnaths of the type p-bars and shield-shaped bar is described for the first time; the latter character is different from the smooth bar-shaped paragnaths in Area VI as has previously been described in these taxa.  © 2007 The Linnean Society of London, Zoological Journal of the Linnean Society , 2007, 150 , 145–176.     

Revision of the Fabriciinae genus Fabriciola Friedrich, 1939 (Polychaeta: Sabellidae)

The Sabellidae polychaete genus Fabriciola Friedrich is revised as a result of examination of as much of the type material as possible. The type species for the genus has been confused. The earliest designation appears to be Fabricia (Manayunkia) spongicola Southern, 1921, by Ushakov [ Akad. Nauk. SSSR, Opredeliteli po Faune SSSR 56: 1–445 (1955)], whereas subsequent works have incorrectly referred to Manayunkia pacifica Annenkova, 1934, as the type species. The following species are redescribed: Fabriciola baltica Friedrich, 1939, F. berkeleyi Banse, 1956, F. ghardaqa Banse, 1959 a . A new species, F. mediaseta, is described. A neotype is designated for F . baltica. Existence of the type material of F. spongicola (Southern), F. pacifica (Annenkova), and F. tonerella Banse, 1959 b is unknown, but these species are discussed in relation to species examined.     

Revision of the type species of Sigalion, Thalenessa and Eusigalion (Polychaeta: Sigalionidae)

The type species of Sigalion Audouin & Milne Edwards, 1830 (5. mathildae), Thalenessa Baird, 1866 (S. edwardsi Kinberg, 1856) and Eusigalion Augener, 1918 (E. vazensis) are re-examined. Since they were first described all three genera have been variously misrepresented, but are currently distinguished by the presence (Thalenessa; syn. Eusigalion) or absence (Sigalion) of a median antenna. Material examined in the present study indicates that S. mathildae also possesses a median antenna. Thalenessa and Eusigalion are considered to be junior synonyms of Sigalion and the generic placings of all species attributed to these genera are investigated.     

Revision of the genus Heliomantis Giglio-Tos 1915 (Insecta: Mantodea: Hymenopodidae)

Summary. The little-known flower mantis genus Heliomantis Giglio-Tos 1915 (Hymenopodidae) distributed in South and South-Eastern Asia is revised. All species are redescribed. New data on the morphology, distribution and ecology are given, and all known specimens are listed. The lectotype of H. elegans (Navás 1904) is designated. Due to highly divergent morphology, H. latipennis Werner 1930 from Sarawak, Borneo, is transferred to Werneriana n. gen., leaving the genus Heliomantis with the only species, H. elegans (Navás, 1904).     

Coelomocytes of Nephtys coeca (Annelida,Polychaeta)

Coelomocytes of Nephtys coeca were studied by transmission electron microscopy. The majority of the coelomocytes were found to be structurally identical with the muscle cells of the body wall. Animals kept under unfavourable conditions tended to have an increased number of coelomocytes and a decreased thickness of the body wall. The muscular coelomocytes, probably released from the body wall, showed various degrees of decomposition, indicating a process of autophagy.     

Spirorbinae (Polychaeta:Serpulidae) from the Red Sea, including descriptions of a new genus and four new species

A new genus, a new subgenus, four new species and four previously described species are recorded from the Red Sea. The new genus Anomalorbis has four and a half thoracic segments. Re-discovery of the sinistral variety of Janua (Dexiospira) steueri confirms Sterzinger's observation that this species may coil in either direction. Janua (Fauveldora) anticorrugata sp. nov. is also sinistral and a shallow water species. It therefore appears that the Red Sea may have been the centre of origin for sinistral mutants of the Janua complex. Other of the new forms live in fairly deep water. The assemblage encountered shows closest affinity with the Indo-Pacific, but suggests a high degree of endemism, which may be related to the high temperatures prevailing at all depths in the Red Sea.     

Giant pelagic larvae of Phyllodocidae (Polychaeta,Annelida)

The microscopic anatomy of giant pelagic larvae of Phyllodocidae was studied using routine histological, SEM, and TEM techniques. The larvae consist of two distinct regions: a large spherical trochophore measuring up to 2 mm in diameter and a posterior, long (up to 10 mm length), narrow rudiment of the adult body with up to 120 segments. The larvae have an unusual mixture of larval and adult features, including a very complex, well-developed brain and ganglia in the ventral nerve cord, and only a single pair of protonephridia located in the hyposphere of the trochophore. A muscular pharynx is not developed. The intestinal wall, especially in the trochophore region, consists of endodermal cells containing considerable nutritive material in the form of yolk-like globular inclusions. The digestive tract of all larvae was empty. The position of the frontal sensory organ and the prototroch, the structure of the parapodia and setae, and the three pairs of tentacular cirri dictate inclusion of the larvae in the family Phyllodocidae. The relatively enormous size and unusual pattern of development of the adult body may be adaptations for a long pelagic life and rapid settlement of the species, which inhabits slopes of islands and underwater mounts located far apart. J. Morphol. 238:93–107, 1998. © 1998 Wiley-Liss, Inc.     

Behaviour, Setal Inversion and Phylogeny of Sabellida (Polychaeta)

The path taken by the faecal groove, following two right angle bends, appears inefficient in Sabellidae. It fits well with the thoracic folds of serpulids and follows a gentle spiral in caobangiids, but only in spirorbids is it of obvious adaptive value, being suited to life in a coiled tube. The associated setal inversion is not necessary for locomotion, which does not depend wholly on setal leverage, except in the smaller Fabriciinae where long-shafted uncini also thrust actively against the elastic tube wall. The collar setae of spirorbids and some serpulids thrust anteriorly, giving some backward movement, but such motion is mainly by body contraction. Short uncini are virtually passive, engaged by opposing setae acting as distance pieces. Some broad bladed setae have a hollow structure around a central core. Pick-axe setae of Sabellinae may have developed to counteract the thrust of respiratory peristalsis. This is not seen in spirorbids and serpulids, the thoracic folds of which are a sufficient respiratory supplement to the tentacles. — Numbers of thoracic segments in Sabellidae range from 1 to 16, and the abdomen becomes vestigial in some Fabriciinae. Abdominal inversion is important to spirorbids but not to sabellids, which are more varied. It seems that the former are archaic and the latter had a coiled ancestry. Sabellariids also show abdominal inversion suggesting a distant relationship with Sabellida.     

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.     

Phylogeny of nereidids (Polychaeta, Nereididae) with paragnaths

A phylogenetic analysis was conducted of the Nereidinae — those members of the Nereididae (Polychaeta) with pharyngeal paragnaths. We had two objectives: to test the monophyly of currently accepted genera, subgenera and informal subgeneric groupings within the Nereidinae, and, if warranted, to propose a more natural classification of the Nereidinae. Parsimony analyses were undertaken, including 52 terminal taxa from all genera and informal groupings from the large heterogeneous genera Nereis , Ceratonereis , Neanthes and Perinereis . Analyses of a character set of 52 informative characters yielded more than 10 000 equally parsimonious trees with a length of 176 steps (consistency index [CI] = 0.34, retention index [RI] = 0.66). Reweighting three times resulted in 445 most parsimonious trees with length 54.62 (CI = 0.59, RI = 0.79). Many characters widely used in nereidid systematics were found to exhibit high levels of homoplasy. The most parsimonious trees could not be rooted such that the selected ingroup, 'Nereididae with paragnaths', was monophyletic, causing us to reject the monophyly of the Nereidinae as currently defined. The following genera were well supported by the parsimony analyses and are newly diagnosed: Alitta , Ceratonereis , Pseudonereis , Simplisetia , Solomononereis and Unanereis . Alitta succinea , Pseudonereis cortezi , Pseudonereis noodti and Pseudonereis pseudonoodti are proposed as new combinations. The parsimony analysis supported the monophyly of neither Composetia , Neanthes , Nereis and Perinereis nor of any new groupings of remaining species presently placed in those genera. It is these poorly supported genera that comprise most species of Nereididae.     

Revision of the subfamily Meyliinae De Coninck, 1965 (Nematoda: Desmoscolecoidea) with a discussion of its systematic position

The Meyliinae contains seven species, belonging to four genera: Boucherius Decraemer & Jensen, 1982, Gerlachius Andrassy, 1976, Meylia Gerlach, 1956 and Noffsingtria Decraemer & Jensen, 1982, differentiated from each other primarily by the ornamentation of the body cuticle. The Meyliinae are compared with the Desmoscolecidae ( sensu Lorenzen, 1969; Timm, 1970) and found to be unique in the position and structure of the amphids and in the reflexed branches of the female reproductive system. It is concluded that they belong to the Desmoscolecida, closely related to the Tricominae.     

Position and Delineation of Chrysopetalidae and Hesionidae (Annelida,Polychaeta, Phyllodocida)

Previous studies suggest that the polychaete taxa Hesionidae and Chrysopetalidae may not represent separate groups, that Pilargidae constitute a subgroup within Hesionidae, and that Hesionides and Microphthalmus are highly derived hesionids. Phylogenetic systematic analyses of Phyllodocida and the subgroup Nereidiformia are presented in order to clarify the position and delineation of these taxa. The phyllodocida analysis includes 18 families representing the majority of the taxa in the group, is rooted with Onuphidae, and is based on 42 absent/present coded morphological characters, obtained mainly from literature. All 69 resulting shortest trees include the clade (Chrysopetalidae, Nereididae, Hesionidae), but with either Syllidae, Nautiliniellidae, Pilargidae or (Aphroditiformia, Pisionidae) as sister. In- and outgroup taxon selection for the Nereidiformia study is dictated by the outcome of Phyllodocida analysis, with scores based on examined species of two chrysopetalids, four hesionids, one nereid, one pilargid, one pisionid, one syllid, plus the putative hesionids Hesionides arenaria and Microphthalmus sp. It is based on 46 absent/present coded morphological characters. Two equally parsimonious trees indicate that chrysopetalids and hesionids are well delineated, that pilargids and hesionids are non-overlapping, and that Microphthalmus and Hesionides are not hesionids.     

Setal Structure, Functions and Interrelationships in Spirorbidae (Polychaeta, Sedentaria)

Typical thoracic setae are composed of longitudinally arranged cylinders ending as teeth at the oblique distal surface. Most thoracic 'blades' are rounded in cross section and show bilateral asymmetry. Some have teeth in oblique rows ("cross striations") on the side adjoining the tube wall. Sickle setae found posteriorly on the thorax have distal portions like abdominal setae. These are flat, each composed mainly of a palisade of spatulate units. On one side cylindrical elements may also be present, in patterns which are characteristic of some taxa. Uncini are made of rows (sometimes single) of shorter cylindrical elements with hooked ends pointing anteriorly. Anterior thoracic hooks are usually blunt, but pointed in the genus Janua. The collar setae assist withdrawal into the tube, the abdominal setae help with emergence, whilst other thoracic setae act as distance pieces, pushing the body to anchor the thoracic uncini against the opposite wall. The other uncini are brought into use by the prehensile abdomen. The flaccid ends of the sickle setae are readily lost in some taxa and their development or loss may reflect unimportant variations in strength of the adjacent abdominal field. Fin and blade setae are not very different from simple setae and the natural grouping of the genera into subfamilies shows that changes from one form of collar seta to another have occurred independently several times.     

Ultrastructure and mineral composition of serpulid tubes (Polychaeta,Annelida)

We have studied the tube ultrastructure of 44 recent species from 36 serpulid genera. Twelve distinct ultrastructures are identified. Serpulids possess very diverse tube ultrastructures, in contrast with the traditional point of view. Most species show single‐layered tubes, but 34% of these species have between two and four ultrastructurally different layers. Tubes are mostly bimineralic, and are composed of aragonite and calcite; however, one of the polymorphs is always dominant. All the studied single‐layered tubes with a lamello fibrillar tube ultrastructure are exclusively calcitic; prismatic structures, both in regular or irregular orientation, are either calcitic or aragonitic in composition. There is no correlation between tube mineralogy, and ultrastructure, and marine, brackish, and freshwater environments. We find that 47% of the serpulid species studied possess a unique combination of tube structure characters. © 2008 The Linnean Society of London, Zoological Journal of the Linnean Society, 2008, 154 , 633–650.     

Red muscle fibre and capillary dimensions in different sizes of a tilapia, Oreochromis niloticus (Trewavas)

Measurements of muscle dimensions that affect respiration in relation to body weight were carried out in a tilapia, Oreochromis niloticus . The fish used in all measurements weighed 0.65–812.3 g. The data were analysed with respect to body weight using logarithmic transformations (log Y=log a + b log W ).
The slopes (b) of the log/log regression lines for weight of body trunk red muscle, average cross-sectional area of muscle fibre, average number of capillaries in direct contact with a muscle fibre, average capillary contact length with a fibre as a fraction of average fibre circumference and number of capillaries mm² of fibre cross-sectional area [N_A(cƒ)] were 1.16, 0.221, 0.084, 0.015, and −0.137 respectively.
These results show that there is an increase in muscle cross-sectional fibre area and number of capillaries in contact with muscle fibres whereas number of capillaries supplying a unit area of muscle fibre decreases during development. There is development of new capillaries with increase in cross-sectional area of red muscle fibres.