Nerve Ring Research Articles

Porphyrocrinus daniellalevyae n. sp. (Echinodermata: Crinoidea), a sea lily from the tropical western Atlantic with a unique crown pattern.

Porphyrocrinus daniellalevyae, new species, is described from irregular, hard-substrate, deep island slope habitats in the tropical western Atlantic Ocean (northwestern Bahamas and, probably, Honduras). It represents the first record of the genus from the western Atlantic, and is the first crinoid, living or fossil, known to gradually increase its number of rays with increasing size and, ostensibly, growth. The four known specimens have 8, 12, 14 and 15 radial ossicles, which give rise to undivided arms. The method of augmentation is unknown, although the possibility of autotomy of one and regrowth of two in its place is discussed. Augmentation of radial number may also account for the absence of an aboral nerve ring associated with the radial ring, unlike the arrangement in almost all living crinoids in which the nervous system has been examined. Ligamentary articulations (trifascial synarthries) exhibit fulcral ridge-and groove architecture between arm ossicle pairs that remains to be described for other members of the genus. The species also exhibits a filamentous arm tip lacking pinnules that has only been described for one other species of Porphyrocrinus.

The two nerve rings of the hypostomal nervous system of Hydra vulgaris-an immunohistochemical analysis.

In Hydra vulgaris, physiological and pharmacological evidence exists for a hypostomal circumferential neuro-effector pathway that initiates ectodermal pacemaker activity at tentacular-hypostomal loci coordinating body and tentacle contractions. Here, we describe an ectodermal nerve ring that runs below and between the tentacles, and an anti-GABAB receptor antibody-labeled ring coincident with it. The location of this ring is consistent with the physiology of the hypostomal pacemaker systems of hydra. We also describe a distally located, ectodermal ring of nerve fibers that is not associated with anti-GABAB receptor antibody labeling. The neurites and cell bodies of sensory cells contribute to both rings. The location of the distal ring and its sensory cell neurites suggests an involvement in the behavior of the mouth. Between the two rings is a network of anastomosing sensory and ganglion cell bodies and their neurites. Phase contrast, darkfield, and antibody-labeled images reveal that the mouth of hydra comprises five or six epithelial folds whose endoderm extensively labels with anti-GABAB receptor antibody, suggesting that endodermal metabotrobic GABA receptors are also involved in regulating mouth behavior.

The Anatomical Relationship Between Recurrent Laryngeal Nerve and First Tracheal Ring in Males and Females.

ObjectivesDespite the modern advances in thyroid surgery, recurrent laryngeal nerve (rln) paralysis is still a critical problem. In order to decrease the rate of this complication, rln anatomy has been studied intensively. In our study, we aimed to recognize the relationship of rln and landmarks of the first tracheal ring.MethodsEighty-six female and 18 male patients who were undergone total thyroidectomy were included in this study. Trachea vertical height (tvh), right recurrent laryngeal nerve height (rrh), left recurrent laryngeal nerve height (lrh), right recurrent laryngeal nerve to trachea anterior face median raphe distance (rrd), left recurrent laryngeal nerve to trachea anterior face median raphe distance (lrd), right recurrent laryngeal nerve respect to trachea ratio (rrtr), and left recurrent laryngeal nerve respect to trachea ratio (lrtr) parameters of all patients were measured and compared in males and females using independent t-test and measurements on both right and left sides were compared statistically without sex discrimination.ResultsThere were no significant differences between groups in tvh, rrh, rrd, lrd, rrtr, and lrtr parameters. Lrh parameter was significantly higher in males than in females (P<0.04). Comparison of right and left sides revealed that lrh was significantly higher than rrh (P<0.001), lrd was significantly higher than rrd (P<0.001), and rrtr was significantly higher than lrtr (P<0.001).ConclusionIn this study, we have shown that in all cases the rln was located around the lower half of trachea vertical length and at this level left rln was located significantly deeper than the right side.

Owenia fusiformis - a basally branching annelid suitable for studying ancestral features of annelid neural development.

BackgroundComparative investigations on bilaterian neurogenesis shed light on conserved developmental mechanisms across taxa. With respect to annelids, most studies focus on taxa deeply nested within the annelid tree, while investigations on early branching groups are almost lacking. According to recent phylogenomic data on annelid evolution Oweniidae represent one of the basally branching annelid clades. Oweniids are thought to exhibit several plesiomorphic characters, but are scarcely studied - a fact that might be caused by the unique morphology and unusual metamorphosis of the mitraria larva, which seems to be hardly comparable to other annelid larva. In our study, we compare the development of oweniid neuroarchitecture with that of other annelids aimed to figure out whether oweniids may represent suitable study subjects to unravel ancestral patterns of annelid neural development. Our study provides the first data on nervous system development in basally branching annelids.ResultsBased on histology, electron microscopy and immunohistochemical investigations we show that development and metamorphosis of the mitraria larva has many parallels to other annelids irrespective of the drastic changes in body shape during metamorphosis. Such significant changes ensuing metamorphosis are mainly from diminution of a huge larval blastocoel and not from major restructuring of body organization. The larval nervous system features a prominent apical organ formed by flask-shaped perikarya and circumesophageal connectives that interconnect the apical and trunk nervous systems, in addition to serially arranged clusters of perikarya showing 5-HT-LIR in the ventral nerve cord, and lateral nerves. Both 5-HT-LIR and FMRFamide-LIR are present in a distinct nerve ring underlying the equatorial ciliary band. The connections arising from these cells innervate the circumesophageal connectives as well as the larval brain via dorsal and ventral neurites. Notably, no distinct somata with 5-HT -LIR in the apical organ are detectable in the larval stages of Owenia.Most of the larval neural elements including parts of the apical organ are preserved during metamorphosis and contribute to the juvenile nervous system.ConclusionsOur studies in Owenia fusiformis strongly support that early branching annelids are comparable to other annelids with regard to larval neuroanatomy and formation of the juvenile nervous system. Therefore, Owenia fusiformis turns out to be a valuable study subject for comparative investigations and unravelling ancestral processes in neural development in Annelida and Bilateria in general.Electronic supplementary materialThe online version of this article (doi:10.1186/s12862-016-0690-4) contains supplementary material, which is available to authorized users.

Anatomy, functional morphology, evolutionary ecology and systematics of the invasive gastropod Cipangopaludina japonica (Viviparidae: Bellamyinae)

The anatomy, functional morphology and evolutionary ecology of the Viviparidae, and the subfamily Bellamyinae in particular, are incompletely known. Partly as a result, genealogical relationships within the family remain poorly understood. Because of this lack in knowledge, few informed hypotheses exist on ancestral states, how differences in body plans between the subfamilies evolved, and how the peculiar biogeographic distribution patterns of viviparids have arisen. Here we document the anatomy, morphology, life history and systematics of Cipangopaludina japonica, a Japanese species that has been introduced into North America, to resolve taxonomic confusion and to improve our understanding of how form and function are related in bellamyines. Anatomical and histological examinations demonstrate marked differences between C. japonicaand other bellamyines in the radula, salivary gland, kidney, nerve ring and reproductive organs. Substantial differences also exist between male and female body organization, but conchological differences between sexes in semi-landmark morphometric analyses are limited. The volume of the brood pouch of females, and hence body and shell size, appear to be good predictors of reproductive success, and the species’ ecological versatility may relate to high fecundity and the ability to alternate between feeding modes. Comparing our observations on C. japonicawith other viviparids and basal Architaenioglossa, we identify several persistent misinterpretations in the literature on how form and function are related in viviparids, not in the least as to female reproductive anatomy. Our reinterpretations improve understanding of the evolution of Viviparidae and its subfamilies, and hopefully will allow future workers to isolate key traits that shaped the evolution of viviparids at the taxonomic levels of their interest for more detailed studies.

Four new species of Epacanthion Wieser, 1953 (Nematoda: Thoracostomopsidae) in intertidal sediments of the Nanji Islands from the East China Sea.

Four new species of Epacanthion are described from intertidal sandy sediments in the Nanji Islands National Marine Natural Reserve from the East China Sea. Males of all four new species have short spicules (&lt; 2 anal body diameter) and a characteristic cervical circle of distinctly short and densely arranged setae at the pharyngeal region: Epacanthion hirsutum sp. nov. with a cervical circle of a single row of setae posterior to the nerve ring; E. longicaudatum sp. nov. with a cervical circle of 16 bundles each composed of six setae in two longitudinal rows posterior to the nerve ring; E. fasciculatum sp. nov. with a cervical circle of 18 bundles each composed of about 10 setae posterior to the nerve ring; and E. sparsisetae sp. nov. with a cervical circle of eight bundles each composed of about 10 setae anterior to the nerve ring. Among the known species of Epacanthion, only two species possess these features: E. quadridisci and E. gorgonocephalum. Epacanthion quadridiscus has six bundles of setae situated at the same level of the nerve ring, while E. gorgonocephalum has distinctly dense setae forming a wide band at the pharyngeal region. Epacanthion hirsutum sp. nov. differs from all congeners by the cervical circle composed of a single row of setae. Epacanthion sparsisetae sp. nov. is unique in having the cervical circle of bundles anterior to the nerve ring. Epacanthion longicaudatum sp. nov. differs from E. fasciculatum sp. nov. by the body size and the structure of the cervical circle. An updated diagnostic key to 28 valid species of Epacanthion is proposed.

Aboral nervous system in two Ordovician crinoids: Reconstruction and comparison of Baltic Pentamerocrinus Jaekel and Grammocrinus Eichwald

Two unusual Middle Ordovician crinoid genera from the St. Petersburg Region, Pentamerocrinus Jaekel, 1918 and Grammocrinus Eichwald, 1860, are redescribed. A new species, Pentamerocrinus kosovi sp. nov., is described based on new material and the cup structure in the type species Grammocrinus lineatus, which has previously been known only from stem fragments, is reconstructed. The system of ridges and canals on the internal surface of the cup plates in both genera is described, allowing the reconstruction of the aboral nervous system. It is in general similar to extant crinoids, but the two Ordovician genera differ considerably in structural details. In Pentamerocrinus, ten nerve cords diverge interradially from the ganglionated nerve ring at the cup base and soon are fused in pairs inside the rays. In Grammocrinus, a similar nerve ring also gives rise to ten cords, but they are inside the rays and become fused in the interrays. This distinction in morphology of the nervous systems is correlated with the interradial arrangement of the axial canal angles of the stem in the first case and radial in the second. Therefore, despite general similarity in the structure and arrangement of calyceal plates, the genus Grammocrinus is assigned to the disparid crinoid family Iocrinidae, while the monotypic family Pentamerocrinidae Jaekel, 1918 is regarded as a fam. inc. sed. of inadunate crinoids.

Bursaphelenchus saudi n. sp. (Tylenchina: Aphelenchoididae) found in packaging wood from Saudi Arabia

Bursaphelenchus saudi n. sp., isolated in Ningbo, P.R. China, from Pinus packaging wood imported from Saudi Arabia, is described. It is characterised by four lateral lines, excretory pore located between metacorpus and nerve ring (anterior to median bulb before cultured), presence of a thick vulval flap, post-uterine branch ca two-thirds of the vulva-anus distance long, female tail hook-like (slightly ventrally bent before cultured), long and conical, tapering to a bluntly rounded terminus, spicules transversely striated with weakly developed rostrum and condylus, a single precloacal papilla and three pairs of ventro-sublateral papillae (one pair precloacal, two pairs postcloacal just anterior to bursal flap and adjacent to each other). It belongs to the africanus-group of the genus Bursaphelenchus and is most close to B. paraburgeri, B. burgermeisteri and B. obeche. It is distinguished from other Bursaphelenchus species by morphology, ITS-RFLP patterns and partial 18S, ITS and 28S D2-D3 rDNA gene sequencing results.

Review of the genus Odontophora (Nematoda: Axonolaimidae), with a key to valid species and description of Odontophora atrox sp. n. from the New Zealand coast

Odontophora is a globally distributed marine nematode genus common in intertidal and subtidal sediments. Odontophora is one of the most diverse genus of the family Axonolaimidae with over 30 valid species described to date; however, the last revision of the genus was made over four decades ago. In addition, limited molecular sequence data are available for the Axonolaimidae and relationships among axonolaimid genera have not yet been investigated using molecular tools. Here, an updated list of species and a key for the identification of all 34 valid species is provided, and preliminary analyses of phylogenetic relationships within the Axonolaimidae are conducted using SSU and D2-D3 of LSU molecular sequences. Odontophora atrox sp. n. is described from intertidal sediments of Wellington, North Island of New Zealand, and is characterised by cephalic setae 1.1-1.5 corresponding body diam. long, 12 subcephalic setae, eight of which are slightly shorter and four of which are markedly shorter than the cephalic setae, excretory pore located slightly posterior to the amphids, and nerve ring located at two-thirds to three-quarters of pharynx length from anterior. Males are characterised by weakly arcuate spicules and tapering gubernacular apophyses, 9-10 small tubular precloacal supplements, cloacal aperture flanked by two sets of heavily cuticularised and eversible spines, and two elongated laterodorsal setae near the tail tip. Preliminary analyses of phylogenetic relationships within the Axonolaimidae provide some support for the monophyly of Odontophora, but drawing more solid inferences about relationships within the Axonolaimidae will require more molecular sequence data of accurately (and verifiably) identified species.

Steinernema beitlechemi n. sp., a new entomopathogenic nematode (Nematoda: Steinernematidae) from South Africa

Steinernema beitlechemin. sp. is a new species of entomopathogenic nematode isolated from soil samples collected in Bethlehem, Free State province, South Africa. The infective juveniles ofS. beitlechemin. sp. are characterised by a body length of 696 (606-768) μm, position of nerve ring of 96 (86-105) μm from the head and lateral fields with six ridges (i.e., seven lines) in mid-body. First-generation males ofS. beitlechemin. sp. can be distinguished by a spicule length of 93 (88-100) μm and 12 pairs of genital papillae. First-generation females have a moderately protruding vulva and a rounded tail tip bearing one spine-like projection. The new species is further characterised by sequences of the ITS and partial 28S regions of the ribosomal DNA. Phylogenetic analyses showS. beitlechemin. sp. as a member of a strongly supported monophyletic clade with three other African species:S. sacchari,S. cameroonenseandS. nyetense.

Nervous system immunohistochemistry of the parasitic cnidarian Polypodium hydriforme at its free-living stage

Polypodium hydriforme, the only species in Polypodiozoa, which is currently considered a class of Cnidaria, and likely a sister group to Medusozoa (together with Myxozoa), is a cnidarian adapted to intracellular parasitism inside sturgeon oocytes. Free-living P. hydriforme lives on river bottoms; it walks on supporting tentacles and uses sensory tentacles to capture food and bring it to the mouth. The nervous system of free-living P. hydriforme was studied by confocal microscopy and immunohistochemistry using antibodies to FMRF-amide and α-tubulin combined with phalloidin-staining of F-actin fibres. A sensory FMRF-amide immunoreactive (IR) nerve net and an α-tubulin IR nerve net have been identified. The FMRF-amide IR nerve net underlies the epidermis along the tentacles and around the mouth; it consists of neurites emanating from epidermal sensory cells and basiepidermal ganglion cells, and it connects with cnidocytes. A deeper-lying α-tubulin IR nerve net occurs only in tentacles and looks like chains of different-sized beads crossing the mesoglea and entwining muscles. Anti-α-tubulin staining also reveals microtubules in muscle cells following the longitudinal muscle fibres or the thin circular F-actin fibres of the tentacles. Cnidocytes in the tentacles are embedded in a regular hexagonal non-neural network formed by the tubulin IR cytoskeleton of epidermal cells. Cnidocils of the cnidocytes around the mouth and in walking tentacles are identical, but those in sensory tentacles differ in length and width. The possible homology of the tubulin IR nerve net with motor nerve nets of cnidarians is discussed. The absence of a classic nerve ring around the mouth and the lack of specialised sense organs are considered to be plesiomorphic characters for Cnidaria.

From nerve net to nerve ring, nerve cord and brain--evolution of the nervous system.

The puzzle of how complex nervous systems emerged remains unsolved. Comparative studies of neurodevelopment in cnidarians and bilaterians suggest that this process began with distinct integration centres that evolved on opposite ends of an initial nerve net. The 'apical nervous system' controlled general body physiology, and the 'blastoporal nervous system' coordinated feeding movements and locomotion. We propose that expansion, integration and fusion of these centres gave rise to the bilaterian nerve cord and brain.

Neuromuscular development in Patellogastropoda (Mollusca: Gastropoda) and its importance for reconstructing ancestral gastropod bodyplan features.

Within Gastropoda, limpets (Patellogastropoda) are considered the most basal branching taxon and its representatives are thus crucial for research into evolutionary questions. Here, we describe the development of the neuromuscular system in Lottia cf. kogamogai. In trochophore larvae, first serotonin‐like immunoreactivity (lir) appears in the apical organ and in the prototroch nerve ring. The arrangement and number of serotonin‐lir cells in the apical organ (three flask‐shaped, two round cells) are strikingly similar to those in putatively derived gastropods. First, FMRFamide‐lir appears in veliger larvae in the Anlagen of the future adult nervous system including the cerebral and pedal ganglia. As in other gastropods, the larvae of this limpet show one main and one accessory retractor as well as a pedal retractor and a prototroch muscle ring. Of these, only the pedal retractor persists until after metamorphosis and is part of the adult shell musculature. We found a hitherto undescribed, paired muscle that inserts at the base of the foot and runs towards the base of the tentacles. An apical organ with flask‐shaped cells, one main and one accessory retractor muscle is commonly found among gastropod larvae and thus might have been part of the last common ancestor.

The plastic nervous system of Nemertodermatida

Nemertodermatida are microscopic marine worms likely to be the sister group to acoels, forming with them the earliest extant branch of bilaterian animals, although their phylogenetic position is debated. The nervous system of Flagellophora cf. apelti, Sterreria spp. and Nemertoderma cf. westbladi has been investigated by immunohistochemistry and confocal microscopy using anti-tubulin, anti-5-HT and anti-FMRFamide antibodies. The nervous system of F. cf. apelti is composed of a large neuropile and a loose brain at the level of the statocysts with several nerve fibres surrounding them and innervating the broom organ. Sterreria spp. shows a commissural-like brain and several neurite bundles going frontad and caudad from this. At the level of the statocysts there is also a thicker aggregation of immunoreactive fibres. The nervous system of N. cf. westbladi consists of a nerve ring lying outside the body wall musculature at the level of the statocyst and a pair of ventro-lateral neurite bundles, from which extend thinner fibres innervating the ventral side of the animal. Numerous bottle-shaped glands were observed, innervated by fibres starting both from the brain and the neurite bundles. The nervous system of the nemertodermatids studied to date displays no common pattern; instead, there is considerable plasticity in the general morphology of the nervous system. In addition, the musculature of Sterreria spp. has been studied by phalloidin staining. It shows diagonal muscles in the anterior quarter of the body and a simple orthogonal grid in the posterior three quarters, being simpler than that of the other nemertodermatids. High-resolution differential interference contrast microscopy permitted to better visualize some morphological characters of the species studied, such as statocysts, sperm and glands and, in combination with anti-tubulin staining, describe in detail the broom organ in F. cf. apelti. Finally, we note an apparent absence of innervation of the gut in Nemertodermatida similar to the condition in Xenoturbella.

Swedish Plectida (Nematoda). Part 10. The genus Deontolaimus de Man, 1880.

The genus Deontolaimus de Man, 1880 is revised and the genus Camacolaimus de Man, 1889 is considered a junior synonym of Deontolaimus based on re-examination of type material of Camacolaimus tardus de Man, 1889 and C. barbatus Warwick, 1970. Two known and three new species of Deontolaimus are described from bottom sediments collected in marine habitats of Sweden: Deontolaimus uniformis (Cobb, 1920) comb. n., D. longicauda (de Man, 1922) comb. n., Deontolaimus catalinae sp. n., D. paraguillei sp. n. and Deontolaimus timmi sp. n. Deontolaimus catalinae sp. n. is characterized by body length of 1.3-1.7 mm; anterior-most somatic sensilla located short distance posterior to amphid; cephalic sensilla equal to 0.2 labial region diameter in length; amphidial fovea ventrally-unispiral with one turn, located in front of cephalic sensilla bases; excretory pore located short distance posterior to onchiostyle base; onchiostyle with bluntly rounded tip and subcylindrical body; male with alveolar supplements extending from anterior end to middle of body, tubular supplements absent; spicules 36-40 µm long; and didelphic female reproductive system. Deontolaimus paraguillei sp. n. is characterized by body length of 1.4-1.8 mm; anterior-most somatic sensilla located at level with onchiostyle; cephalic sensilla equal to 0.2-0.3 labial region diameter in length; amphidial fovea ventrally-unispiral with one turn, located at level with cephalic sensilla bases; excretory pore located just posterior to nerve ring level; onchiostyle with bluntly rounded tip and subcylindrical body; male with alveolar supplements extending from anterior end to about three body diameters in front of cloaca, tubular supplements absent; spicules 42-46 µm long; and didelphic female reproductive system. Deontolaimus timmi sp. n. is characterized by body length of 0.7-0.9 mm; anterior-most somatic sensilla located at level with onchiostyle; cephalic sensilla equal to 0.2-0.3 labial region diameter in length; amphidial fovea ventrally-unispiral with one turn, located just in front of cephalic sensilla bases; excretory pore located just posterior to nerve ring level; onchiostyle with triangular tip with bluntly rounded apex and strongly sclerotized dorsal edge, and subcylindrical body; male with alveolar supplements extending from anterior end to anterior part of intestine, tubular supplements absent; spicules 28 µm long; and didelphic female reproductive system. The following nomenclatorial changes are proposed: genera Acontiolaimus Filipjev, 1918, Camacolaimoides De Coninck & Schuurmans Stekhoven, 1933, Camacolaimus de Man, 1889, Digitonchus Cobb, 1920 and Ypsilon Cobb, 1920 are synonimized with the genus Deontolaimus de Man, 1880; Camacolaimus reykjanesi De Coninck, 1943 and Camacolaimus glauxicola Allgén, 1951a are considered junior synonyms of Deontolaimus papillatus de Man, 1880; Camacolaimus barbatus apud Pastor de Ward, 1984 is described as the separate species Deontolaimus catalinae sp. n.; Camacolaimus tardus apud Lorenzen, 1969 is considered to be the separate species Deontolaimus lorenzeni nom. n.; Camacolaimus tardus apud Timm, 1963 is described as the separate species Deontolaimus timmi sp. n.; Camacolaimus barbatus Warwick, 1970 is considered a junior synonym of Deontolaimus tardus (de Man, 1889) comb. n.; Camacolaimus parvus Timm, 1961 is transferred to the genus Deontolaimus as D. parvus (Timm, 1961) comb. n.; Digitonchus cylindricaudatus Chitwood, 1951 is transferred to the genus Deontolaimus as D. cylindricaudatus (Chitwood, 1951) comb. n.; Ypsilon exile Cobb, 1920 is transferred to the genus Deontolaimus as D. exilis (Cobb, 1920) comb. n.; Camacolaimus guillei de Bovee, 1977 is transferred to the genus Deontolaimus as D. guillei (de Bovee, 1977) comb. n.; Camacolaimus longicauda de Man, 1922 is transferred to the genus Deontolaimus as D. longicauda (de Man, 1922) comb. n.; Camacolaimus monhystera Gerlach, 1967 is transferred to the genus Deontolaimus as D. monhystera (Gerlach, 1967) comb. n.; Camacolaimus pontollittoralis Uzunov, 1977 is transferred to the genus Deontolaimus as D. pontollittoralis (Uzunov, 1977) comb. n.; Camacolaimus praedator de Man, 1922 is transferred to the genus Deontolaimus as D. praedator (de Man, 1922) comb. n.; Camacolaimus prytherchi Chitwood, 1935 is transferred to the genus Deontolaimus as D. prytherchi (Chitwood, 1935) comb. n.; Camacolaimus tardus de Man, 1889 is transferred to the genus Deontolaimus as D. tardus (de Man, 1889) comb. n.; Camacolaimus trituberculatus Blome, 1982 is transferred to the genus Deontolaimus as D. trituberculatus (Blome, 1982) comb. n.; and Digitonchus uniformis Cobb, 1920 is transferred to the genus Deontolaimus as D. uniformis (Cobb, 1920) comb. n. A taxonomic review and identification key for species of the genus Deontolaimus are also given.

Description of Aegialoalaimus bratteni sp. n. from Skagerrak and a review of the genus (Aegialoalaimidae, Nematoda incertae sedis).

BackgroundThe genus Aegialoalaimus de Man, 1907 includes 12 nominal species, of which three species are considered valid, two species were transferred to other genera and seven species have uncertain taxonomic status.New informationNew species, Aegialoalaimus bratteni sp. n. was found in Skagerrak off the west coast of Sweden. It is particularly characterized by the 1.5-1.8 mm long body, short papilliform cephalic sensilla, excretory pore opening just posterior to nerve ring level, spicules that are straight in shape, supplements and gubernaculum absent, separating it from other valid species of the genus. It can be further differentiated from Aegialoalaimus elegans in having longer body (1.5-1.8 mm in A. bratteni sp. n. vs 0.8-1.3 mm in A. elegans), shape and size of spicules (straight and 22-29 µm long in A. bratteni sp. n. vs arcuate and 34 µm long in A. elegans), absence of precloacal supplements (vs seven-eight in A. elegans), absence of gubernaculum (vs present in A. elegans); from A. setosa in having shorter tail (c´=2.6-3.1 in A. bratteni sp. n. vs c´=4.2 in A. setosa), shorter cephalic sensilla (0.5-1.0 µm in A. bratteni sp. n. vs 9 µm in A. setosa), shape and size of spicules (straight and 22-29 µm long in A. bratteni sp. n. vs arcuate and 40-45 µm long in A. setosa), absence of precloacal supplements (vs eight in A. setosa), absence of gubernaculum (vs present in A. setosa); from A. leptosoma in having longer body (1.5-1.8 mm in A. bratteni sp. n. vs 0.5-0.7 mm in A. leptosoma) and other measurements, shape of spicules (straight in A. bratteni sp. n. vs arcuate in A. leptosoma), absence of precloacal supplements (vs three-five in A. leptosoma), absence of gubernaculum (vs present in A. leptosoma). Type specimens of Aegialoalaimus cylindricauda Allgén, 1933 and A. paratenuicaudatus Allgén, 1959 are redescribed and taxonomic status of these two species is re-evaluated. A taxonomic review, tabular compendium and identification key for species of the genus Aegialoalaimus are also given.

A Morphological and Molecular Study of Spectatus spectatus (Kathlaniidae), Including Redescription of the Species and Amendment of Genus Diagnosis.

Spectatus spectatus Travassos, 1923 (Nematoda: Kathlaniidae) found in the intestine of Piaractus mesopotamicus (Holmberg, 1887) (Characiformes: Serrasalmidae) from the River Miranda, Mato Grosso do Sul, Brazil is redescribed based on morphological evaluation of newly collected material and examination of type and voucher specimens from the Coleção Helmintológica do Instituto Oswaldo Cruz. The following characteristics previously unreported or insufficiently described were observed: morphology of lips, presence of lamellae-like supplementary lips, presence of pharynx and cuticular ring surrounding the oral opening associated with a complex cuticular apparatus anterior to the pharynx, the number and arrangement of caudal papillae (13 pairs plus 1 unpaired), and the position of nerve ring. Since S. spectatus is the type species of Spectatus, the diagnosis of this Neotropical genus is amended. Synonymy of Chabaudinema Díaz-Ungría, 1968 with Spectatus, first proposed in 1980 by Baker, is supported by the present data. Molecular data that include the first sequence of the SSU rDNA for any species of Spectatus indicate a basal position of S. spectatus within Cosmocercoidea, forming a distant lineage from that comprising 2 species of Falcaustra Lane, 1915. This separate position of S. spectatus supports validity of the genus.

Neural development in the tardigrade Hypsibius dujardini based on anti-acetylated α-tubulin immunolabeling

BackgroundThe tardigrades (water bears) are a cosmopolitan group of microscopic ecdysozoans found in a variety of aquatic and temporarily wet environments. They are members of the Panarthropoda (Tardigrada + Onychophora + Arthropoda), although their exact position within this group remains contested. Studies of embryonic development in tardigrades have been scarce and have yielded contradictory data. Therefore, we investigated the development of the nervous system in embryos of the tardigrade Hypsibius dujardini using immunohistochemical techniques in conjunction with confocal laser scanning microscopy in an effort to gain insight into the evolution of the nervous system in panarthropods.ResultsAn antiserum against acetylated α-tubulin was used to visualize the axonal processes and general neuroanatomy in whole-mount embryos of the eutardigrade H. dujardini. Our data reveal that the tardigrade nervous system develops in an anterior-to-posterior gradient, beginning with the neural structures of the head. The brain develops as a dorsal, bilaterally symmetric structure and contains a single developing central neuropil. The stomodeal nervous system develops separately and includes at least four separate, ring-like commissures. A circumbuccal nerve ring arises late in development and innervates the circumoral sensory field. The segmental trunk ganglia likewise arise from anterior to posterior and establish links with each other via individual pioneering axons. Each hemiganglion is associated with a number of peripheral nerves, including a pair of leg nerves and a branched, dorsolateral nerve.ConclusionsThe revealed pattern of brain development supports a single-segmented brain in tardigrades and challenges previous assignments of homology between tardigrade brain lobes and arthropod brain segments. Likewise, the tardigrade circumbuccal nerve ring cannot be homologized with the arthropod ‘circumoral’ nerve ring, suggesting that this structure is unique to tardigrades. Finally, we propose that the segmental ganglia of tardigrades and arthropods are homologous and, based on these data, favor a hypothesis that supports tardigrades as the sister group of arthropods.Electronic supplementary materialThe online version of this article (doi:10.1186/s13227-015-0008-4) contains supplementary material, which is available to authorized users.

Modern Data on the Innervation of the Lophophore in Lingula anatina (Brachiopoda) Support the Monophyly of the Lophophorates.

Evolutionary relationships among members of the Lophophorata remain unclear. Traditionally, the Lophophorata included three phyla: Brachiopoda, Bryozoa or Ectoprocta, and Phoronida. All species in these phyla have a lophophore, which is regarded as a homologous structure of the lophophorates. Because the organization of the nervous system has been traditionally used to establish relationships among groups of animals, information on the organization of the nervous system in the lophophore of phoronids, brachiopods, and bryozoans may help clarify relationships among the lophophorates. In the current study, the innervation of the lophophore of the inarticulate brachiopod Lingula anatina is investigated by modern methods. The lophophore of L. anatina contains three brachial nerves: the main, accessory, and lower brachial nerves. The main brachial nerve is located at the base of the dorsal side of the brachial fold and gives rise to the cross neurite bundles, which pass through the connective tissue and connect the main and accessory brachial nerves. Nerves emanating from the accessory brachial nerve account for most of the tentacle innervation and comprise the frontal, latero-frontal, and latero-abfrontal neurite bundles. The lower brachial nerve gives rise to the abfrontal neurite bundles of the outer tentacles. Comparative analysis revealed the presence of many similar features in the organization of the lophophore nervous system in phoronids, brachiopods, and bryozoans. The main brachial nerve of L. anatina is similar to the dorsal ganglion of phoronids and the cerebral ganglion of bryozoans. The accessory brachial nerve of L. anatina is similar to the minor nerve ring of phoronids and the circumoral nerve ring of bryozoans. All lophophorates have intertentacular neurite bundles, which innervate adjacent tentacles. The presence of similar nerve elements in the lophophore of phoronids, brachiopods, and bryozoans supports the homology of the lophophore and the monophyly of the lophophorates.

Morphology and neurochemistry of rabbit iris innervation

The aim of this study was to map the entire nerve architecture and sensory neuropeptide content of the rabbit iris. Irises from New Zealand rabbits were stained with antibodies against neuronal-class βIII-tubulin, calcitonin gene-related peptide (CGRP) and substance P (SP), and whole-mount images were acquired to build a two-dimensional view of the iridal nerve architecture. After taking images in time-lapse mode, we observed thick nerves running in the iris stroma close to the anterior epithelia, forming four to five stromal nerve rings from the iris periphery to the pupillary margin and sub-branches that connected with each other, constituting the stromal nerve plexus. In the anterior side, fine divisions derivated from the stromal nerves, forming a nerve network-like structure to innervate the superficial anterior border layer, with the pupillary margin having the densest innervation. In the posterior side, the nerve bundles ran along with the pupil dilator muscle in a radial pattern. The morphology of the iris nerves on both sides changed with pupil size. To obtain the relative content of the neuropeptides in the iris, the specimens were double stained with βIII-tubulin and CGRP or SP antibodies. Relative nerve fiber densities for each fiber population were assessed quantitatively by computer-assisted analysis. On the anterior side, CGRP-positive nerve fibers constituted about 61%, while SP-positive nerves constitute about 30.5%, of the total nerve content, which was expressed as βIII tubulin-positive fibers. In addition, in the anterior stroma of the collarette region, there were non-neuronal cells that were positive for SP. On the posterior side, CGRP-positive nerve fibers were about 69% of total nerve content, while SP constituted only up to 20%. Similarly, in the trigeminal ganglia (TG), the number of CGRP-positive neurons significantly outnumbered those that were positive for SP. Also, all the SP-positive neurons were labeled with CGRP. This is the first study to provide a two-dimensional whole mount and a cross-sectional view of the entire iris nerve architecture. Considering the anatomical location, the high expression of CGRP and SP suggests that these neuropeptides may play a role in the pathogenesis of anterior uveitis, glaucoma, cataracts and chronic ocular pain.