Anna Zhadan

The morphology of Laubieriopsis sp. (Polychaeta, Fauveliopsidae) and the position of fauveliopsids in the polychaete system

The external and internal morphology of Laubieriopsis sp. from the North Sea was studied using light, scanning, and transmission microscopy. The morphology of the head end, parapodia, pigidium, body cavity, digestive tract, nervous system, and reproductive system was analyzed. The studied species was most similar to L. cabiochi (Amoreux, 1982) but displayed some significant differences. The body consists of 22 setigers (versus 21 setigers of L. cabiochi), bears bidentate modified aciculae in four anterior segments, and has paired genital papillae (unpaired in L. cabiochi) located on the eighth segment. Parapodia of the 5th–22nd segments bear one long capillary chaeta and one very short and thin chaeta in each ramus. The anterior part of the body capable of invaginating (forming an introvert) comprises only the prostomium and peristomium and does not include the first segment, as is typical of flabelligerids. The oral cavity contains well-developed dorsolateral ciliary folds. The ventral pharyngeal organ is undetectable. The ciliary folded esophagus is a straight tube without a loop even in an inverted head. The gut forms a small loop in the region of the 17th segment. The body cavity is divided by well-developed dissepiments and mesenteries, forming an intricate system of partitions in the anterior part of the body. The neuron bodies of the ventral nerve cord are homogenously distributed without forming distinct ganglia; however, the nerve cord forms two or three swellings in each segment. The position of fauveliopsids in the polychaete system is discussed. This study did not find any traits of fauveliopsids similar to Flabelligeridae and close taxa.

Ontogenetic development and functioning of the anterior end of Cossura pygodactylata Jones, 1956 (Annelida: Cossuridae)

Abstract Juvenile and adult Cossura pygodactylata Jones 1956 from the White Sea were studied using confocal laser scanning microscopy, light microscopy, scanning and transmission electron microscopy. Transformations of the anterior musculature and digestive tract during ontogenesis were investigated. The early juveniles were shown to be lecithotrophic; their pharyngeal cavities were not connected to the intestines, which contained yolk granules. The juveniles bore prototrochs, which are used for movement, although juveniles had parapodial musculature similar to that of the adults. The juveniles presumably inhabit the upper semi-liquid layer of the silt. The muscles of the prostomium and circumbuccal complex change dramatically during ontogenesis. The ultrastructure of the buccal tentacles is redescribed. The tentacles consist of outer ciliated epithelial cells and an inner cylinder formed by epithelio-muscle cells. The blood sinus is situated between the central cylinder and the epithelium. Both juveniles and adults have developed circulatory systems. The whole dorsal vessel forms the heart with walls that consist of cells with circular cross-striated muscular fibres. The inner lumen is occluded by the heart body which is formed by a single row of cells that are tightly pressed together and connected by adherens junctions along their anterior and posterior surfaces. They contain granules and vesicles and bear numerous processes on the outer surface. The heart body most likely has a secretory haemopoetic function. A hypothetical mechanism of protraction and retraction of the buccal tentacles is suggested, and the participation of muscle contraction and relaxation in these movements is described. It is proposed that the protraction of the tentacles is provided by cell rigidity and increases in the blood volume in the tentacles blood sinuses. The development of the circulatory system is likely related to the need to keep the tentacles exposed during feeding while the anterior part of the body cavity is filled with muscle cell processes and there is no coelomic liquid flow. The proposed mechanism of feeding inside the sediment contrasts with that of surface feeding suggested by Tzetlin (Mém Mus Natl Hist Nat 162:137–143, 1994).

The fine structure of epidermal papillae of Travisia forbesii (Annelida)

The structure of the epidermis of Travisiaforbesii was described using light and electron microscopy. The epidermis is a highly modified variant of the normal one-layer polychaete epithelium. It consists of basal epidermal cells and an external layer of closely sited papillae consisting of glandular and supportive epidermal cells, and extensive electron-transparent intercellular spaces. The papillae are embedded in the thick cuticle. Each papilla has a peduncle, which is formed by one cell that penetrates the inner cuticle layer to the basal epidermal cells. A fold of basement membrane forms the core of the peduncle and ends in the base of a papilla. All epidermal cells are connected to each other with apical cell junctions and to the basement membrane with hemidesmosomes, so the epithelium is continuous and uninterrupted. The epidermis has an intra-epidermal neuron plexus. The structure of the papillae is compared with papillae and tubercles of other polychaetes, and the possible functional significance and phylogenetic implications of these structures are discussed.

A new species of Fauveliopsidae (Annelida) from the North Sea

Abstract A new species of the genus Laubieriopsis Petersen, 2000 is described based on 28 specimens collected in the north-east part of the North Sea. It is characterized by fixed number of chaetigers (22), paired genital papillae, bidentate neurochaeta of chaetigers 1–4, the absence of acicular chaetae on chaetigers 5–21 and, on the last chaetiger, one acicular and three capillary chaetae enlarged and directed backward. The present study brings the number of known species of Laubieriopsis to five and the number of Northeast Atlantic species of this genus to two.

Comparative study of the diaphragm (gular membrane) in Terebelliformia (Polychaeta, Annelida)

The structure and location of the diaphragm (gular membrane) was studied in five families of Terebelliformia: Terebellidae, Trichobranchidae, Pectinariidae, Ampharetidae and Alvinellidae, using dissections, histology, and scanning and transmission electron microscopy. Position, shape, and structure of the diaphragm differ in these taxa. In Terebellidae and Pectinariidae the diaphragm is straight. In Trichobranchidae, Ampharetidae and Alvinellidae it is funnel-shaped. Diaphragm possesses two contractile sacs in Terebellidae and Pectinariidae, one in Alvinellidae and none at all in Trichobranchidae. The relative size and form of the sacs varied. Representatives of the family Ampharetidae have one or two sacs or none at all. Four kinds of the diaphragm can be distinguished: strait with two sacs, funnel-shaped with two sacs, funnel-shaped with one sac, funnel-shaped without sacs. In some Alvinellidae, the diaphragm is fenestrated, while in all other taxa it is continuous. The wall of the sacs is more muscular than the wall of the remaining diaphragm. The diaphragm is attached to the body wall at different levels: between the third and fourth segments in pectinariids or between the fourth and fifth in terebellids, ampharetids, alvinellids and trichobranchids. In most cases, the diaphragm contains two coelothelial layers with a well-developed extracellular matrix in between, and one or two muscle layers. The maximum development of the muscle fibres occurs in Terebellidae; probably related to the length of buccal tentacles. Significance of morphological and ultrastructural peculiarities of the diaphragm is discussed.

Orbiniidae (Annelida: Errantia) from Lizard Island, Great Barrier Reef, Australia with notes on orbiniid phylogeny.

The fauna of Orbiniidae (Annelida: Errantia) from the Lizard Island has been studied. Five species were found and each was redescribed and illustrated using light microscopy and SEM. Scoloplos acutissimus Hartmann-Schröder, 1991 and Scoloplos dayi Hartmann-Schröder, 1980 collected for the first time since their original descriptions and confirmed through re-examination of their type materials. Molecular analyses were carried out using nuclear 18S rDNA and mitochondrial 16S rDNA and CO1 gene sequences with evolutionary distances and the Neighbor-Joining Method. The molecular analyses did not support the monophyly of the genera Scoloplos, Leitoscoloplos, Leodamas, and Naineris, and its results are incongruent with morphological data.

Sternaspidae (Annelida, Sedentaria) from Vietnam with description of three new species and clarification of some morphological features

Five sternaspid species were found near Vietnam shores: Sternaspis britayevi sp. nov., S. costata von Marenzeller, 1879, S. nana sp. nov., S. papillosa sp. nov., and S. spinosa Sluiter 1882. Sternaspis britayevi is described from the shallow water in Vietnam inhabiting soft bottoms; it resembles S. spinosa described from Java and S. thorsoni Sendall & Salazar-Vallejo, 2013 described from the Persian Gulf, but differs in having a medially projected and markedly ribbed fan of the ventro-caudal shield and nearly parallel, distally widened and rounded branchial plates. Sternaspis nana sp. nov. is described from Nha Trang Bay; it differs from the other known species by the combination of the following characters: small size, evenly distributed micropapillae and regular rows of long cirriform papillae; posterior chaetal fascicles consisting of single thick chaeta; a ventral shield with smooth integument, without ribs and usually without concentric lines. Sternaspis papillosa sp. nov. is also described from Nha Trang Bay; it resembles S. africana Augener, 1918 and S. andamanensis Sendall & Salazar-Vallejo, 2013 by having similar ventro-caudal shields but differs by body papillation and details of the ventro-caudal shield. Based upon observations of different species some morphological features are clarified: 1) notochaetae are present in introvert chaetigers as delicate capillaries; 2) peg-chaetae are really a dense group of more than 100 thin individual chaetae, embedded in a fibrous matrix, and covered by a common sheath; 3) the pharynx is an eversible, lobed, axial non-muscular proboscis with a ciliated surface; 4) the body cavity is divided by three septa in the anterior body region, and there are no other septa; and 5) an eversible anal peduncle is confirmed, as has been shown by early taxonomists.

Two new species of Cossura (Cossuridae, Annelida) from the terminal lobes of the Congo River deep-sea fan

Two new species of Cossura Webster & Benedict, 1887 were found in material collected during sampling from the terminal lobes of the Congo deep-sea fan. They were described using light and scanning electron microscopy. Cossura platypus sp. nov. has 15–17 thoracic chaetigers, a prostomium longer than it is wide, with a widely rounded anterior margin, an abruptly expanded posterior prostomial ring the same length as the peristomium, without a mid-ventral notch, a branchial filament attached to the midlength of chaetiger 3, and a pygidium with three anal cirri. Cossura platypus sp. nov. is similar to C. brunnea Fauchald, 1972 but differs in the shape of the prostomium, which is widely rounded anteriorly in C. platypus sp. nov. and is broadly triangular in C. brunnea ; furthermore, C. platypus sp. nov.is uniformly pale, whereas C. brunnea has dark pigmentation. Cossura candida Hartman, 1955 differs from C. platypus sp. nov. in the conical shape of the prostomium and 24–35 thoracic chaetigers. Cossura flabelligera sp. nov. has 16–19 thoracic chaetigers, a conical prostomium, and a branchial filament arising from the posterior part of chaetiger 2; the entire body, including the chaetae, is covered by a thick mucous sheath similar to the tunic of flabelligerids. Cossura flabelligera sp. nov. resembles C. longocirrata Webster & Benedict, 1887 in the position of the branchial filament, the shape of the prostomium, and the number of thoracic chaetigers; it differs in having a thick mucous sheath. This character seems to be unique for the Cossuridae.

Comparative morphology and ultrastructure of the respiratory system in four species of the Opheliidae family

Polychaetes show a remarkable diversity of the respiratory system structures. However, the ultrastructure of gills was studied only in some species from several families. The morphology and ultrastructure of the gills of Ophelia limacina, Ophelina acuminata, Euzonus arcticus, and Travisia forbesii (Opheliidae) were studied using light microscopy, scanning electron microscopy, and transmission electron microscopy. Gills could be interpreted as body wall protrusions containing coelom, blood lacunas, or vessels connected to interepithelial blood sinuses. The blood is separated from the environment by a 1.5-μm thick wall in E. arcticus, 2-μm in O. limacine and T. forbesii, and 3-μm in O. acuminata, which is close to the minimum observed in the polychaetes; it refers to the effective gas exchange. Unlike the other species, the gill surface lacks cilia in T. forbesii. This might be explained by the fact that the body of T. forbesii is covered with a thick layer of mucus making cilia inefficient and leading to their reduction. The cuticle of the gills is thin; its structure in O. acuminata, O. limacina, and E. arcticus resembles the cuticle covering the other part of the body. In T. forbesii, the gills are covered with a protocuticle close to that in larval forms of polychaetes. The epidermal cells of gills are different in form in all four species studied. The epithelial cells in E. arcticus have few organelles, but contain numerous vacuoles, which represent a low level of synthesis. Therefore, they are likely to have a support function. The epithelium in O. limacina, O. acuminata, and E. arcticus has multiple gland cells, while T. forbesii does not have any. The gills of O. acuminata contain glands of two types, while O. limacine and E. arcticus have only one type of gill gland. The epidermal cells in T. forbesii are connected by desmosomes, while in the other three species, they also have dense junctions, and even adhesive belts in O. limacina and E. arcticus. The coelom is lined with mioepithelium, and in E. arcticus, together with podocites. Blood cells of O. limacina, O. acuminata, and E. arcticus were found for the first time, while in O. limacina, amoebocytes form an incomplete endothelium on basal lamina. The gills of T. forbesii differ from those of the other three Opheliid species in anatomy and some ultrastructural features. These data together with the results of recent molecular studies could be one more reason to exclude Travisia from Opheliidae. Furthermore, several common anatomic and ultrastructural features of O. limacina, O. acuminata, and E. arcticus could serve as a synapomorphy of the family Opheliidae. However, further anatomical and ultrastructural investigations are necessary before we can use this character for phylogenetic analysis.