Tubeworm succession at hydrothermal vents: use of biogenic cues to reduce habitat selection error?

Species colonizing new deep-sea hydrothermal vents along the East Pacific Rise show a distinct successional sequence: pioneer assemblages dominated by the vestimentiferan tubeworm Tevnia jerichonana being subsequently invaded by another vestimentiferan Riftia pachyptila, and eventually the mussel Bathymodiolus thermophilus. Using a manipulative approach modified from shallow-water ecological studies, we test three alternative hypotheses to explain the initial colonization by T. jerichonana and its subsequent replacement by R. pachyptila. We show that R. pachyptila and another vestimentiferan, Oasisia alvinae, colonized new surfaces only if the surfaces also were colonized by T. jerichonana. This pattern does not appear to be due to restricted habitat tolerances or inferior dispersal capabilities of R. pachyptila and O. alvinae, and we argue the alternative explanation that T. jerichonana facilitates the settlement of the other two species and is eventually outcompeted by R. pachyptila. Unlike the classic model of community succession, in which facilitating species promote their own demise by modifying the environment to make it more hospitable for competitors, we suggest that T. jerichonana may produce a chemical substance that induces settlement of these competitors. This process of selecting habitat based on biogenic cues may be especially adaptive and widespread among later-successional species that occupy a physically variable and unpredictable environment. In these cases, the presence of weedy species implies some integrated period of environmental suitability, whereas an instantaneous assessment of physical habitat conditions, such as water temperature for vent tubeworms, provides a poorer predictor of long-term habitat suitability. Received: 13 July 1999 / Accepted: 2 November 1999     

The morphology and anatomy of the vestimentiferan worm <Emphasis Type="Italic">Oasisia alvinae</Emphasis> Jones, 1985 (Annelida: Siboglinidae). II. Integument,nervous system and musculature

The histological structure of the epidermis, nervous system, and musculature of the vestimentiferan worm Oasisia alvinae is examined. The differentiation of the integument of different regions of the body and the histological structure of the pyriform glands and papillae with cuticular plaques are described. All the main elements of the nervous system lie in the thickness of the epidermis. The brain structure is examined and an attempt is made to homologize parts of the vestimentiferan brain with the polychaete brain. Part of the vestimentiferan brain above the intrabrain channel corresponds to the supraesophageal ganglion of polychaetes, while part of the vestimentiferan brain under the channel corresponds to the subesophageal ganglion. Two commissures are located in the brain region that corresponds to the supraesophageal ganglion. These commissures could be related to the ventral and dorsal roots of the circumesophageal connectives of sedentary polychaetes. Bundles of fiber occur, which presumably correspond to the circumesophageal connectives and the transverse commissure inside the subesophageal ganglion. The musculature differentiation in the trunk region is a characteristic feature of O. alvinae, i.e., feather-like muscles that occur only in the anterior part of the trunk.     

The morphology and anatomy of the vestimentiferan worm <Emphasis Type="Italic">Oasisia alvinae</Emphasis> Jones, 1985 (Annelida: Siboglinidae). I. External morphology,obturaculae and tentacles

This study describes the tube structure, external morphology, and histological organization of the obturacula and tentacles of the small hydrothermal-vent vestimentiferan worm Oasisia alvinae. The tubes are considerably twisted and bear collars, thus suggesting a step-like growth of the worm. The total length of the studied specimens is 32–41 mm. The trunk region comprises 75% of the total body length and is differentiated into a broadened forepart and a narrowed posterior part. The ratio between the lengths of the obturacular and vestimental regions is 0.62–0.63. The examined specimens of O. alvinae have 13 to 17 pairs of tentacular lamellae; the total number of tentacles is about 550. The muscular bands in the obturacula of O. alvinae lie in the parafrontal planes. Polymorphism occurs in the number and arrangement of the denticles of the opistosomal chaetae in O. alvinae.     

Ultrastructure of tentacles in the sipunculid worm <Emphasis Type="Italic">Thysanocardia nigra</Emphasis> Ikeda, 1904 (Sipuncula)

The ultrastructure of the tentacles was studied in the sipunculid worm Thysanocardia nigra. Flexible digitate tentacles are arranged into the dorsal and ventral tentacular crowns at the anterior end of the introvert of Th. nigra. The tentacle bears oral, lateral, and aboral rows of cilia; on the oral side, there is a longitudinal groove. Each tentacle contains two oral tentacular canals and an aboral tentacular canal. The oral side of the tentacle is covered by a simple columnar epithelium, which contains large glandular cells that secrete their products onto the apical surface of the epithelium. The lateral and aboral epithelia are composed of cuboidal and flattened cells. The tentacular canals are lined with a flattened coelomic epithelium that consists of podocytes with their processes and multiciliated cells. The tentacular canals are continuous with the radial coelomic canals of the head and constitute the terminal parts of the tentacular coelom, which shows a highly complex morphology. Five tentacular nerves and circular and longitudinal muscle bands lie in the connective tissue of the tentacle wall. Similarities and differences in the tentacle morphology between Th. nigra and other sipunculan species are discussed.Original Russian Text Copyright © 2005 by Biologiya Morya, Maiorova, Adrianov.     

High‐contiguity genome assembly of the chemosynthetic gammaproteobacterial endosymbiont of the cold seep tubeworm Lamellibrachia barhami

Symbiotic relationships between vestimentiferan tubeworms and chemosynthetic Gammaproteobacteria build the foundations of many hydrothermal vent and hydrocarbon seep ecosystems in the deep sea. The association between the vent tubeworm Riftia pachyptila and its endosymbiont Candidatus Endoriftia persephone has become a model system for symbiosis research in deep‐sea vestimentiferans, while markedly fewer studies have investigated symbiotic relationships in other tubeworm species, especially at cold seeps. Here we sequenced the endosymbiont genome of the tubeworm Lamellibrachia barhami from a cold seep in the Gulf of California, using short‐ and long‐read sequencing technologies in combination with Hi‐C and Dovetail Chicago libraries. Our final assembly had a size of ~4.17 MB, a GC content of 54.54%, 137X coverage, 4153 coding sequences, and a CheckM completeness score of 97.19%. A single scaffold contained 99.51% of the genome. Comparative genomic analyses indicated that the L. barhami symbiont shares a set of core genes and many metabolic pathways with other vestimentiferan symbionts, while containing 433 unique gene clusters that comprised a variety of transposases, defence‐related genes and a lineage‐specific CRISPR/Cas3 system. This assembly represents the most contiguous tubeworm symbiont genome resource to date and will be particularly valuable for future comparative genomic studies investigating structural genome evolution, physiological adaptations and host‐symbiont communication in chemosynthetic animal‐microbe symbioses.     

The anatomy of the blood vascular system of the giant vestimentiferan tubeworm Riftia pachyptila (Siboglinidae,Annelida)

The giant dimensions of vestimentiferan Riftia pachyptila (Jones, 1981 ) are achieved thanks to the well‐developed vascular system. In the vestimentum, there is a complicated net of lacunae, including the brain blood supply and the ventral lacuna underlying the ciliary field. The trunk region has an extensive network of blood vessels feeding the gonads («rete mirabile»). The thick muscular lining of the mesenterial vessels in the trunk and the dorsal vessel in the opisthosome serves as an additional pump, pushing blood into numerous vessels in the segments. It was hypothesized that the blood envelope of the ventral blood vessel in the trunk provides the blood supply to the trophosome. The 3D reconstruction has revealed that there are two vascular systems of the tentacular crown of R. pachyptila . Blood runs into the tentacles via axial afferent vessels, as described earlier only for Riftia , and also via basal ones, as described for other vestimentiferans except Riftia . The basal ones are poorly developed, and the number of lamellar blood vessels is small, indicating a lack of demand for these within huge R. pachyptila . It appears that the presence of these vessels is the preserved ancestral state of Vestimentifera. In different portions of the dorsal vessel, the morphology of the intravasal body varies, depending on function.     

Primary structure of the common polypeptide chain b from the multi-hemoglobin system of the hydrothermal vent tube worm Riftia pachyptila: An insight on the sulfide binding-site

The deep-sea tube worm Riftia pachyptila Jones possesses a multi-hemoglobin system with three different extracellular Hbs: two dissolved in the vascular blood, V1 (ca. 3,500 kDa) and V2 (ca. 400 kDa), and one in the coelomic fluid, C1 (ca. 400 kDa). V1 Hb consists of four heme-containing, globin chains (b–e) and four linker chains (L1–L4). V2 and C1 Hbs are exclusively built from globin chains, six for V2 (a–f) and five for C1 (a–e). The complete amino acid sequence of the isolated monomeric globin chain b, common to all Riftia Hbs, has been determined by automated Edman degradation sequencing of the peptides derived by digestion with trypsin, chymotrypsin, thermolysin, and CNBr. This polypeptide chain is composed of 144 amino acid residues, providing a Mr of 16, 135.0 Da. Moreover, the primary sequence of chain b revealed 3 Cys residues at position 4, 75, and 134. Cys-4 and Cys-134 are located at positions where an intra-chain disulfide bridge is formed in all annelid, vestimentiferan, or pogonophoran chains, but Cys-75 is located at a unique position only found in three globin chains belonging to Lamellibrachia and Oligobrachia, a vestimentiferan and a pogonophoran. In both groups, Hbs can bind sulfide reversibly to fuel the chemosynthetic process of the symbiotic bacteria they harbor. Sulfide-binding experiments performed on purified Hb fractions (i.e., V1, V2, and C1 Hbs) suggest that free Cys residues on globin chains, and the numerous Cys found in linker chains, as determined previously by ESI-MS, may be the sulfide binding-sites. Blocking the free Cys by N-ethylmaleimide, we confirmed that free cysteines were involved in sulfide-binding but did not account for the whole sulfide-binding capacity of V1 Hb. Furthermore, a phylogenetic tree was constructed from 18 globin-like chains of annelid, vetimentiferan, and pogonophoran extracellular Hbs to clarify the systematic position of tubeworms. Riftia chain b clearly belongs to the “strain A” family with 30 to 80% identity with the other sequences analyzed. Its position in the tree confirmed a close relationship between vestimentiferan, pogonophoran, and annelid Hbs. Proteins 29:562–574, 1997. © 1997 Wiley-Liss, Inc.     

On the phylogeny of the Phyllodocidae (Polychaeta Annelida): an alternative

The phylogeny of the Phyllodocidae (Polychaeta Annelida) is examined in an analysis which includes previously unnoticed characters of the nervous system. Concentrating on four problems of importance in understanding the phylogeny of the family, a study of the nervous system demonstrated that: 1. A median antenna, such as that present in species of Eulalia, is not homologous to the nuchal papilla of, for example, Eteone and Phyllodoce; 2. Nuchal organs, presumably found in all phyllodocids, are basically homologous, but four separate types may be recognized; 3. The anterior concentration of the first segments (particularly their tentacular cirri), which is evident in most phyllodocids, is accompanied by different alterations of the ventral nervous system. The polarities of these changes are not self-evident; 4. A study of the ventral nervous system of Eteone reveals that the first apparent segment, bearing two pairs of tentacular cirri, must be regarded as homologous to the second segment of all other phyllodocids. Furthermore, this genus descended from forms in which a segment was present anterior to the first apparent segment, the first two segments possibly bearing tightly packed tentacular cirri. In connection with other characters, this information was used to produce a cladogram, which has some surprising features. The most unexpected result is the prediction that Eteone is the sister group of a taxon containing the genera Paranaitis, Chaetoparia, and Phyllodoce. The results are discussed and compared to those of other investigators.     

Ultrastructure of the sensory epithelia of oral tube,fungiform sensory bodies,and terminal knobs of tentacles of Ovatella myosotis Draparnaud (Archaeopulmonata,Gastropoda)

Sensory epithelia of the oral tube, a fungiform body anterior to the tentacles and of the terminal knob of tentacles, were studied in Ovatella myosotis by electron microscopy. All three epithelia consist of columnar support cells, sensory cells, and, except in the oral tube, numerous goblet cells. The epithelia differ significantly in their apical differentiations. In the oral tube an outer layer is formed by irregularly bent villi of support cells completely embedded in a surface coat. Cilia and cytofila of the dendrites of sensory cells intertwine throughout the entire depth of the villous layer. In the fungiform sensory body some of the villi of support cells are singly branched. Their basal region is free of a surface coat. In this region cytofila and cilia of dendrites form a spongy layer, some cytofila extending into the surface coat. In the tentacular terminal knob the villi of the support cells branch dichotomously once or twice, a single villus thus ending with 2–4 tips. Only these terminal twigs are invested with the surface coat. The cytofila and dendritic cilia are confined to a broad spongy layer underneath. Three types of dendrites are present. They differ in their number of cilia, structure of basal bodies and occurrence in the three epithelia. Dendritic cytofila are most abundant in the tentacular terminal knob and least numerous in the oral tube. The observations are discussed with respect to corresponding epithelia in other pulmonates, the homology of the fungiform body, and possible functional correlates of structural features.     

Modulation of two oscillatory networks in the peripheral olfactory system by γ‐aminobutyric acid,glutamate, and acetylcholine in the terrestrial slug Limax marginatus

The digit‐like extensions (the digits) of the tentacular ganglion of the terrestrial slug Limax marginatus are the cell body rich region in the primary olfactory system, and they contain primary olfactory neurons and projection neurons that send their axons to the olfactory center via the tentacular nerves. Two cell clusters (the cell masses) at the bases of the digits form the other cell body rich regions. Although the spontaneous slow oscillations and odor responses in the tentacular nerve have been studied, the origin of the oscillatory activity is unknown. In the present study, we examined the contribution of the neurons in the digits and cell masses to generation of the tentacular nerve oscillations by surgical removal from the whole tentacle preparations. Both structures contributed to the tentacular oscillations, and surgical isolation of the digits from the whole tentacle preparations still showed spontaneous oscillations. To analyze the dynamics of odor‐processing circuits in the digits and tentacular ganglia, we studied the effects of γ‐aminobutyric acid, glutamate, and acetylcholine on the circuit dynamics of the oscillatory network(s) in the peripheral olfactory system. Bath or local puff application of γ‐aminobutyric acid to the cell masses decreased the tentacular nerve oscillations, whereas the bath or local puff application of glutamate and acetylcholine to the digits increased the digits' oscillations. Our results suggest the existence of two intrinsic oscillatory circuits that respond differentially to endogenous neurotransmitters in the primary olfactory system of slugs. © 2004 Wiley Periodicals, Inc. J Neurobiol 59: 304–318, 2004     

Previously unrecognized stages of species‐specific colonization in the mutualism between Xenorhabdus bacteria and Steinernema nematodes

The specificity of a horizontally transmitted microbial symbiosis is often defined by molecular communication between host and microbe during initial engagement, which can occur in discrete stages. In the symbiosis between Steinernema nematodes and Xenorhabdus bacteria, previous investigations focused on bacterial colonization of the intestinal lumen (receptacle) of the nematode infective juvenile (IJ), as this was the only known persistent, intimate and species‐specific contact between the two. Here we show that bacteria colonize the anterior intestinal cells of other nematode developmental stages in a species‐specific manner. Also, we describe three processes that only occur in juveniles that are destined to become IJs. First, a few bacterial cells colonize the nematode pharyngeal‐intestinal valve (PIV) anterior to the intestinal epithelium. Second, the nematode intestine constricts while bacteria initially remain in the PIV. Third, anterior intestinal constriction relaxes and colonizing bacteria occupy the receptacle. At each stage, colonization requires X. nematophila symbiosis region 1 (SR1) genes and is species‐specific: X. szentirmaii, which naturally lacks SR1, does not colonize unless SR1 is ectopically expressed. These findings reveal new aspects of Xenorhabdus bacteria interactions with and transmission by theirSteinernema nematode hosts, and demonstrate that bacterial SR1 genes aid in colonizing nematode epithelial surfaces.     

Scanning electron microscopy of glochidia and juveniles of the freshwater mussel,Hyriopsis myersiana

Summary

The ultrastructure of early stages of the mussel, Hyriopsis (Limnoscapha) myersiana (Lea, 1856), was observed by scanning electron microscopy from the glochidial period until the onset of the juvenile stage 10 days later. Further observations were performed for an additional 13 days to assess juvenile development. Glochidia extracted from the brood chambers have a hookless, semi-oval and equivalve calcareous shell with numerous pores in the internal surface, pits in the external surface and cuticular spines in the ventral region. Keratin fibers with a random arrangement in the cuticle of the glochidial shell were also detected. The appearance of the foot within 10 days of in vitro glochidial culture was considered the main feature of metamorphosis to the juvenile stage. Another change during the following 13 days was the formation of a new periostracum exhibiting growth lines under the old glochidial shell. This development occurs mainly in the anterior region and is followed by hardening of the periostracum matrix by calcium deposition. Periostracum growth gradually became apparent in the lateral and posterior regions at the end of this period. The retraction of spines and the alteration of the external surface of the old shell are also described. It is speculated that transcuticular filaments identified in the juvenile stage may have sensory or metabolic exchange functions. The prominent foot, gradually covered by long dense cilia, shows rhythmical movements which suggest a role in feeding. Similarly, cilia present in the mantle may also be involved in the capture of food, while microvilli may facilitate absorption of dissolved materials. Longer cilia, sparsely distributed in the mantle, may function as chemo- or tactile sensors.     

Dynamics of cell proliferation and apoptosis reflect different life strategies in hydrothermal vent and cold seep vestimentiferan tubeworms

Deep-sea vestimentiferan tubeworms, which live in symbiosis with bacteria, exhibit different life strategies according to their habitat. At unstable and relatively short-lived hydrothermal vents, they grow extremely fast, whereas their close relatives at stable and long-persisting cold seeps grow slowly and live up to 300 years. Growth and age differences are thought to occur because of ecological and physiological adaptations. However, the underlying mechanisms of cell proliferation and death, which are closely linked to homeostasis, growth, and longevity, are unknown. Here, we show by immunohistochemical and ultrastructural cell cycle analyses that cell proliferation activities of the two species studied are higher than in any other characterized invertebrate, being only comparable with tumor and wound-healing processes. The slow growth in Lamellibrachia luymesi from cold seeps results from balanced activities of proliferation and apoptosis in the epidermis. In contrast, Riftia pachyptila from hydrothermal vents grows fast because apoptosis is down-regulated in this tissue. The symbiont-housing organ, the trophosome, exhibits a complex cell cycle and terminal differentiation pattern in both species, and growth is regulated by proliferation. These mechanisms have similarities to the up- and down-regulation of proliferation or apoptosis in various types of tumor, although they occur in healthy animals in this study, thus providing significant insights into the underlying mechanisms of growth and longevity. Financial support was provided by the Austrian Science Foundation (FWF; grants to M.B.), a DOC scholarship from the Austrian Academy of Science (to B.P.), and grants from the US National Science Foundation (to C.R. Fisher).     

Cellular structure and ultrastructure of the black coral Antipathes aperta: 1. Organization of the tentacular epidermis and nervous system

The tentacular epidermis of the black coral Antipathes aperta is organized into three distinct regions, containing at least nine different types of cells. The outermost region is dominated by spirocytes along with two types of nematocytes, organized into discrete wart-like batteries. The two nematocyte types both contain microbasic b-mastigophore nematocysts. The outer boundary of the wart is marked by the presence of both spumous and vesicular mucus cells. The ciliation of the wart is contributed principally by the spirocytes. Warts are enveloped and separated from one another by an unusual neurosensory cell complex that extends from the tentacular surface to the mesogleal connective tissue foundation. Funnel-like, flagellated cells composing the complex connect with ganglion cells composing the dominant portion of the nerve net system. Branches of this complex also penetrate the central portion of the wart, making direct contact with the cnidae. The tentacular mid-region is composed of nematocytes and spirocytes in various stages of maturation, along with epitheliomuscular cell (EMC) somata. The EMC's narrow apically extend toward the tentacle surface, forming contacts with the cnidae. The basal end of the EMC expands to form the larger portion of the tentacular musculature. The inner region of tentacular epidermis is marked by a neuromuscular complex sheathed by extensions of mesoglea. The ganglion cells occur as a plexus deep within the tentacle and form polarized junctions with the EMC's, but neuromuscular synapses are not well enough defined for documentation. Polarized synapses lacking well-defined membrane thickenings characterize the interneuronal junctions. Granular cells lining the mesogleal surface appear to be responsible for mesogleal fibrillogenesis.     

The Morphology of the Phoronid Phoronopsis harmeri

We studied the morphology and gross anatomy of the phoronid Phoronopsis harmeriusing light microscopy and scanning electron microscopy. The body of Ph. harmeriis subdivided into several regions: a lophophore, a head, anterior, and posterior parts of the body, and an ampulla. The lophophore is spiral and comprises 0.5 turns. In males, there are lophophoral organs in the tentacular crown; under the lophophore, there is an epithelial fold or collar. The internal organization shows partitioning into three coeloms: the coelom of the epistome, the tentacular coelom, and the trunk coelom. The trunk coelom is divided into a series of chambers by a complex system of mesenteries. The intestine is U-shaped, and the epistome is located above the mouth opening. The circulatory system is closed and consists of the following vessels: the efferent and afferent circular, left and right lateral (efferent), and medial (afferent) vessels. In Ph. harmeri, there is a dorsolateral (afferent) vessel running through the ampulla and the lower part of the posterior trunk region. The excretory system is composed of paired metanephridia that resemble asymmetrical U-shaped tubes. Sexual dimorphism is characteristic of the structure of the distal part of the nephridium, which opens into the body cavity. The nervous system consists of a dorsal nervous field, a circular nerve plexus, and a giant left nerve fiber. Ph. harmeriis a dioecious species; the gametes develop in a vasoperitoneal tissue that envelops the intestine in the posterior part of the trunk region.     

Fine structure of the dioptric apparatus in the stalk eye of Onchidium verruculatum (Gastropoda, Stylommatophora): a distinct lamellar substructure of the lens

 The dioptric apparatus of the stalk eye in Onchidium verruculatum, including a tentacular epidermis, a cornea, and a lens, was examined using transmission electron microscopy. The tentacular epidermis was formed by columnar epidermal cells, sensory dendrites, and glandular cells. The cornea was an anterior part of the eye vesicle and consisted of corneal cells which contained abundant glycogen particles but no dark pigment granules in their cytoplasm. An acellular, transparent, ellipsoidal lens was located in the center of the eye vesicle. The lens showed a marginal zone, an outer zone, a transitional zone, an inner zone, and a central region arranged concentrically. The outer zone was the most intense electron-dense region and was finely granular in structure. The marginal zone was also finely granular and surrounded the outer zone with many hair-like slender strands on the retinal side. Toward the center of the lens this homogeneous fine granularity gradually changed into globular or rod-like substructures, about 30 nm in diameter, and then abruptly transformed into a lamellar substructure of about 30 nm in thickness. The inner zone contained a mosaic of lamellar substructures which were arranged in a fingerprint pattern that was particularly enhanced with periodic acid methenamine silver proteinate staining. The center itself consisted of deformed lamellar substructures. The concentric arrangement of substructures inside the lens of the O. ver-ruculatum stalk eye is probably responsible for the concentration and/or refraction of light. Accepted: 5 December 1997     

Identification and Characterization of a Flagellin Gene from the Endosymbiont of the Hydrothermal Vent Tubeworm Riftia pachyptila

The bacterial endosymbionts of the hydrothermal vent tubeworm Riftia pachyptila play a key role in providing their host with fixed carbon. Results of prior research suggest that the symbionts are selected from an environmental bacterial population, although a free-living form has been neither cultured from nor identified in the hydrothermal vent environment. To begin to assess the free-living potential of the symbiont, we cloned and characterized a flagellin gene from a symbiont fosmid library. The symbiont fliC gene has a high degree of homology with other bacterial flagellin genes in the amino- and carboxy-terminal regions, while the central region was found to be nonconserved. A sequence that was homologous to that of a consensus ς²⁸ RNA polymerase recognition site lay upstream of the proposed translational start site. The symbiont protein was expressed in Escherichia coli, and flagella were observed by electron microscopy. A 30,000-M_r protein subunit was identified in whole-cell extracts by Western blot analysis. These results provide the first direct evidence of a motile free-living stage of a chemoautotrophic symbiont and support the hypothesis that the symbiont of R. pachyptila is acquired with each new host generation.     

Disconnection of a basal ganglia circuit in juvenile songbirds attenuates the spectral differentiation of song syllables

Similar to language acquisition by human infants, juvenile male zebra finches (Taeniopygia guttata) imitate an adult (tutor) song by transitioning from repetitive production of one or two undifferentiated protosyllables to the sequential production of a larger and spectrally heterogeneous set of syllables. The primary motor region that controls learned song is driven by a confluence of input from two premotor pathways: a posterior pathway that encodes the adult song syllables and an anterior pathway that includes a basal ganglia (BG)‐thalamo‐cortical circuit. Similar to mammalian motor‐learning systems, the songbird BG circuit is thought to be necessary for shaping juvenile vocal behaviour (undifferentiated protosyllables) toward specific targets (the tutor's song syllables). Here, we tested the hypothesis that anterior pathway activity contributes to the process of protosyllable differentiation. Bilateral ablation of lateral magnocellular nucleus of the anterior nidopallium (LMAN) was used to disconnect BG circuitry at ages before protosyllable production and differentiation. Comparison to surgical controls revealed that protosyllables fail to differentiate in birds that received juvenile LMAN ablation—the adult songs of birds with >80% bilateral LMAN ablation consisted of only one or two syllables produced with the repetitive form and spectral structure that characterizes undifferentiated protosyllables in normal juveniles. Our findings support a role for BG circuitry in shaping juvenile vocal behaviour toward the acoustic structure of the tutor song and suggest that posterior pathway function remains in an immature “default” state when developmental interaction with the anterior pathway is reduced or eliminated. © 2013 Wiley Periodicals, Inc. Develop Neurobiol 74: 574–590, 2014     

<Emphasis Type="Italic">Doederleinia gracilispinis</Emphasis> (Fowler, 1943), a junior synonym of <Emphasis Type="Italic">Doederleinia berycoides</Emphasis> (Hilgendorf, 1879), with review of the genus

A poorly known acropomatid, Rhomboserranus gracilispinis Fowler, 1943, was originally described on the basis of specimens from the Philippines. Since the recognition of Rhomboserranus as a junior synonym of Doederleinia, R. gracilispinis had been considered a valid species of Doederleinia. Examination of the holotype of R. gracilispinis and other type series of nominal species of Doederleinia showed them to be included in the single species D. berycoides (Hilgendorf, 1879). The sole representative of Doederleinia is distributed from Japan to northwestern Australia. This species is distinguishable from other acropomatids by the following combination of characters: head and body red; nine dorsal-fin spines; three anal-fin spines; no luminous organ; a row of conical teeth with a large canine tooth medially on lower jaw; large conical teeth on anterior part of outer margin with two or three large canine teeth on inner margin on upper jaw; and anus situated just anterior to origin of anal fin.     

Setal variability of <Emphasis Type="Italic">Hydrozetes lemnae</Emphasis> and <Emphasis Type="Italic">H. thienemanni</Emphasis> (Acari: Oribatida: Hydrozetidae)

Setal variability and the other morphological characters of juvenile stages and adult of Hydrozetes lemnae (Coggi, 1897) and H. thienemanni Strenzke, 1943 were investigated. In the juveniles of both species the length and shape of some setae vary, especially in the gastronotic region, more so in H. lemnae, which is parthenogenetic and reproduces by thelytoky, than in H. thienemanni, which is dioecious. The former species usually has more thick setae in the anterior and medial regions of the gastronotum, especially in the larva, compared to the latter. In the juveniles of H. lemnae the prodorsal setae le and in are longer, and in the nymphs the gastronotal setae of the l-series are usually longer than in H. thienemanni. These species differ distinctly by the number of long setae in the posterior part of the nymphs; in H. lemnae three pairs of long setae occur, while in H. thienemanni only two pairs; the respective juvenile stages of H. lemnae are also smaller than those of H. thienemanni. In the adults the number of c-series setae varies, as seta c ₁ is lost, and in some individuals also seta c ₃, and only seta c ₂ remains.