Ultrastructure of Chrysopetalid Paleal Chaetae (Annelida,Polychaeta)

Paleal notochaetae belonging to a number of Chrysopetalum species (Chrysopetalidae) were examined by scanning and transmission electron microscopy. Paleae are composed of broad medullary channels stacked with a regular series of horizontal fibrous diaphragms. The medullary part of the palea is surrounded by irregular rows of narrow tubular channels within the chaetal cortex. The origin and function of camerate chaetae is discussed.     

Ultrastructure and significance of the transitory nephridia in Erpobdella octoculata (Hirudinea, Annelida)

In early developmental stages of Erpobdella octoculata two pairs of transitory nephridia occur which degenerate during the formation of the body segments. Because in the ground pattern of Annelida the first nephridia formed during ontogenesis are protonephridia, it can be assumed that the transitory nephridia of E. octoculata are homologous to the larval protonephridia (head kidneys) of Polychaeta. To test this hypothesis two cryptolarvae of E. octoculata were investigated ultrastructurally. Both pairs of transitory nephridia are serially arranged to either side of the midgut vestigium. Each organ consists of a coiled duct that opens separately to the exterior by an intraepidermal nephridiopore cell. The duct is percellular and formed by seventeen cells. Adluminal adherens and septate junctions connect all duct cells; the most proximal duct cell completely encloses the terminal end of the duct lumen. A filtration structure characteristic for protonephridia is lacking. Additionally, the entire organ lacks an inner ciliation. Morphologically and ultrastructurally the transitory nephridia of E. octoculata show far reaching congruencies with the segmental metanephridia in different species of the Hirudinea. These congruencies support the assumption that formation of transitory nephridia and definitive metanephridia in Hirudinea depends on the same genetic information. The same inherited information is assumed to cause the development of larval head kidneys and subsequently formed nephridia in different species of the Polychaeta. Thus, the presumed identical fate of a segmentally repeated nephridial anlage supports the hypothesis of a homology between the transitory nephridia in Hirudinea species and the protonephridial head kidneys in the ground pattern of the Polychaeta. We, therefore, assume that functional constraints lead to a modification of the protonephridial head kidneys in Hirudinea and explain ultrastructural differences between the transitory nephridia in Hirudinea and the protonephridia in Polychaeta. Accepted: 11 December 2000     

Ultrastructure of gill epithelial cells of Diopatra neapolitana (Annelida,Polychaeta)

Summary The ultrastructure of gill epidermal cells of Diopatra neapolitana and their relationship with blood spaces are described. The existence of a basal infolding complex, related to the blood spaces, is also reported. A possible involvement of these cells in osmoregulation and ion interchange, apart from their well-known role in respiration, is suggested.Abbreviations bc Blood cell - bi Basal infolding - bl Basal lamina - bs Blood space - ci Cilia - cu Cuticle - db Dense body - EC Epidermal cell - Gc Golgi complex - id Interdigitation - j Junction - m Mitochondria - mv Microvilli - n Nucleus - pv Pinocytotic vesicle - rer Rough endoplasmic reticulum     

Zur Struktur der Solenocyten (Cyrtocyten) vonAnaitides mucosa (Annelida,Polychaeta)

Based on electron microscopic observations, the structure of the solenocytes ofA. mucosa is described. The tube of the solenocyte is made up of 14–15 rods. These rods, which are filled with regularly packed filaments, are interconnected by an amorphous to filamentous substance. A single flagellum, lying in the tube, is surrounded by a sheet of amorphous material. The functional organization of the solenocytes is discussed.     

Ultrastructure and functional morphology of the female reproductive organs inProtodrilus (Polychaeta,Annelida)

The morphology and function of the female reproductive organs in 6Protodrilus species are investigated by light- and transmission electron microscopy. Possible ways in which spermatozoa may enter the female coelom after leaving the spermatophore are discussed for species with and without special female reception organs. Only femaleP. rubropharyngeus andP. flavocapitatus have “dorsal organs” for spermatophore reception. The structure and function of these organs are described, as well as those of the oviduct found in 3 of the species investigated. The possible phylogenetic origin of gonoducts and different modes of oviposition within the genus are discussed. Finally, the high taxonomic significance of female traits such as dorsal organs, oviducts, cocoon glands and lateral ciliary rows in this genus is stressed.     

Ultrastructure of the Genital Organs in the Interstitial Syllid Petitia amphophthalma (Annelida,Polychaeta)

Abstract The gonochoristic syllid Petitia amphophthalma is one of the truly interstitial polychaetes. P. amphophthalma does not show any epitokous modifications at maturity such as those that usually occur in syllids. The reproductive structures are unique: the male genital organs consist of a seminal vesicle in chaetigers 6–10, subdivided into a dorsal part tightly filled with spermatozoa and a ventral part with contents in different stages of spermatogenesis, one pair of sperm ducts and conspicuous gland cells situated in chaetigers 10 and 11. Their glandular secretions are discharged into the sperm duct together with those of other types of gland cells that form the duct. The oocytes develop freely within the body cavity of the females. Each of the fertile segments possesses a paired oviduct ending in a large ciliated funnel. Sperm ducts and oviducts are probably modifications of excretory organs; nephridia are absent in segments where gonoducts occur. A direct sperm transfer by lytic opening of the integument of the female and internal fertilization are inferred. Copyright © 1996 Published by Elsevier Science Ltd on behalf of the Royal Swedish Academy of Sciences     

The development of the serpulid Pomatoleios kraussii (Annelida, Polychaeta)

The development of Pomatoleios kraussii is extremely similar to that of Pomatoceros triqueter , and is completed under laboratory conditions in 1–3 weeks at 25–27°C. Mature larvae settle and metamorphose preferentially on the shells of adult conspecifics.     

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.     

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.     

Phylogenetic relationships within Nephtyidae (Polychaeta,Annelida)

Ravara, A., Wiklund, H., Cunha, M. R. & Pleijel, F. (2010). Phylogenetic relationships within Nephtyidae (Polychaeta, Annelida). —Zoologica Scripta, 39, 394–405. We present the first phylogeny of nephtyids, a common, soft‐bottom living polychaete family comprising five genera and over 100 species. Characters used to distinguish nephtyid genera are a matter of controversy and considerable confusion remains as to the generic delineations. The phylogeny is estimated with molecular data from the mitochondrial genes cytochrome oxidase I and 16S rDNA, the nuclear genes 18S rDNA and 28S rDNA and morphological data. The results reveal two well‐supported major clades, corresponding in part to the two main genera of the family, Aglaophamus and Nephtys. The species Nephtys pulchra and Nephtys australiensis are transferred to Aglaophamus, and new diagnoses for the genera are provided. Dentinephtys is synonymized with Nephtys, and Nephtys cornuta is sister to the remaining nephtyids and is referred to the new genus Bipalponephtys, together with Nephtys danida and Micronephthys neotena. Micronephthys is sister to Nephtys and Inermonephtys is of uncertain position.     

Evolution of interstitial Polychaeta (Annelida)

An update of the systematics is given for the eight most important interstitial polychaete families: Diurodrilidae, Nerillidae, Protodrilidae, Protodriloididae, Saccocirridae, Parergodrilidae, Polygordidae and Psammodrilidae. Additional information and new observations are presented for the Diurodrilidae, Nerillidae and Psammodrilidae. Three new supplementary evolutionary hypotheses for these families are here suggested: (I) basal position of Diurodrilidae in Polychaeta, (2) evolution of Nerillidae in mud, and (3) evolution from meio- to macrofaunal forms of Psammodrilidae.     

Development and differentiation of the eye in Platynereis dumerilii (Annelida,Polychaeta)

The nereid polychaete, Platynereis dumerilii, possess two pairs of post-trochophoral eyes with one vitreous body each. The development of these eyes has first been observed in 2-day-old larvae. Whether the eye anlagen arise from stem cells or from undifferentiated ectodermal tissue was not determined. At first, the anlagen of the anterior and the posterior eyes adjoin each other. They separate in late 3-day-old larvae. The first separated eye complexes consist each of two supporting and two sensory cells. The supporting cells synthesize two different kinds of granules, the pigment granules of the pigment cup and the prospective tubules of the vitreous body. These tubules accumulate in the distal process of the supporting cell. The vitreous body is formed by compartments of the supporting cells filled with the osmiophilic vitreous body tubules. The short, bulbar photosensory processes bear microvilli that emerge into the ocular cavity. At the apex of each sensory cell process, a single cilium (or occasionally two) arises. The sensory cells contain a different kind of pigment granule within their necks at the level of the pigment cup. The rate of eye development and differentiation varies. New supporting cells are added to the rim of the eye cup. They contribute to the periphery of the vitreous body like onion skins, and sensory cells move between supporting cells. The older the individual compartments of the vitreous body are, the more densely packed is their content of vitreous body tubules. Elongation of the sensory and supporting cell processes of the older cells increases the volume of the eye. The eyespots of the trochophore are briefly described as of the two-celled rhabdomeric type with a single basal body with ciliary rootlet.     

Syllidae (Annelida, Polychaeta) from the Caribbean coast of Venezuela

Venezuela possesses a great variety of coastal environments allowing for a high diversity of marine species. However, systematic studies on marine invertebrates are scarce, especially on polychaetes. The family Syllidae is poorly known, and only 14 genera and 42 species have been reported from this country. A total of 13 genera and 26 species the Syllidae were identified from benthic samples collected on different substrata of the northeastern coast of Venezuela. Of these, seven genera and 16 species constitute new records for Venezuela: Odontosyllis guillermoi, Syllides floridanus, Salvatoria clavata, Salvatoria limbata, Sphaerosyllis longicauda, Parapionosyllis longicirrata, Trypanosyllis parvidentata, Trypanosyllis vittigera, Opisthosyllis sp., Syllis amica, Syllis armillaris, Syllis gracilis, Syllis pseudoarmillaris, Syllis vittata, Parasphaerosyllis indica and Myrianida convoluta.     

Ultrastructure of the Tubificid Acrosome (Annelida, Oligochaeta)

The later morphogenesis of the acrosome of Limnodriloides winckelmanni and Rhyacodrilus arthingtonae is compared with that in Enchytraeus and in earthworms. After superposition of the acrosome on the tip of the nucleus the manchette continues apically beyond the nucleus to ensheath the acrosomal tube. At the posterior limit of, and probably contained in, the spacious/ terminal primary acrosomal vesicle is an electron-dense ring. A domed protrusion into the floor of the primary vesicle is tentatively regarded as the secondary acrosome vesicle. The axial rod when first observed is attached to the vesicle complex. Later, the rod detaches and extends deeply into the acrosome tube. A membrane ensheathes the tubificid axial rod but its exact homology with the complex layers surrounding the lumbricid or megascolecid axial rod is not clear. The domed apical region of the tubificid acrosome is probably a persistence of the primary acrosome vesicle and it is deduced that the acrosome vesicle surrounding the axial rod in lumbricids and megascolecids is a product, by invagination, of the secondary acrosome vesicle only.     

A morphometric comparison of dissimilar early development in sibling species of Platynereis (Annelida,Polychaeta)

Summary Early development of Platynereis massiliensis was studied in serial sections of fixed embryos and in living or fixed embryos whose nuclei had been made visible with a fluorescent label. The unfertilized egg is an ellipsoid with three axes of differing length. The longest axis corresponds to the dorsoventral axis of the developing embryo. Egg volume is ten times that in the sibling species, P. dumerilii, mainly due to increased yolk content. The timing and spatial pattern of cleavage were observed from first cleavage to the 62-cell stage. Volumes of the blastomeres, their nuclei, their yolk-free cytoplasm and their yolk were determined from serial sections up to the 29-cell stage. In the P. massiliensis embryo, cell cycles are on average 3.7 times longer than in P. dumerilii; volume proportions among the blastomeres also differ and the macromeres containing the bulk of yolk are particularly large, but otherwise the cleavage patterns, differential segregation of yolk and yolk-free cytoplasm, and the histogenetic fates of the blastomeres are the same as in P. dumerilii. This equivalence of cell lineage and of cytoplasmic segregation mechanisms in both species, maintained in spite of the different appearance of the embryos, suggests functional importance of and selective constraint on these developmental features. The relatively accelerated divisions of the 2d cell line in P. massiliensis may be interpreted as the precocious development of cell lines which give rise to adult structures. Several structures, obviously functional in developing P. dumerilii, have lost their function in P. massiliensis: the egg contains few cortical granules, giving rise to only a moderate egg jelly layer in the zygote; prototroch cells develop cilia, but the heavy embryo is unable to swim; the larva develops three pairs of parapodia but, unlike the corresponding stage in P. dumerilii, is not capable of coordinate locomotion. This loss of motility is related to the brooding habit of the species developing inside the parental tube and is explained as the result of a switch from pelagic to benthic, protected reproduction in P. massiliensis. Offprint requests to: A.W.C. Dorresteijn     

Elektronenmikroskopische Untersuchungen anAnaitides mucosa (Annelida,Polychaeta). Cuticula und Cilien,Schleimzellen und Schleimextrusion

Two components, a basal cuticle and an epicuticle, make up the cuticle ofA. mucosa. The basal cuticle consists of collagen fibrils, which are arranged in about 20 layers. The orientation of the fibrils changes rectangularly from one layer to the next. Fine filaments interweave the basal cuticle. The epicuticle, which is covered by a layer of electron dense material, is composed of irregularly arranged thin filaments. Branched microvilli of the epidermal cells penetrate the cuticle. Bacteria are found in the basal cuticle. Dorsally each segment has a band of densely packed smooth cilia. Laterally and partly ventrally aggregates of cilia are observed. These cilia exhibit apically artificial swellings. At least six different mucous cells are observed in the epidermis, morphologically distinguishable by the structure of the secretion products. Mucus is secreted via exocytosis through cuticular pores. During this process the mucus might expand. The secreted mucus consists of filamentous subunits.