Morphology of ctenostome bryozoans: 7. Hislopia, Echinella and Timwoodiellina.

Ctenostome bryozoans are a small group of gymnolaemates comprising less than 400 recent species. They are paraphyletic and ctenostome-grade ancestors gave rise to Cheilostomata, the most dominant and speciose taxon of Bryozoa in the present day. Investigations into ctenostomes are important for reconstructing character evolution among Gymnolaemata. As a continuation of studies on a morphological series of ctenostome bryozoans, we herein investigate six species of hislopiids, a small clade of three genera occurring in freshwater habitats. The general morphology of all species is similar in having primarily uniserial chains of encrusting zooids, which are mostly oval to ellipsoid and have a flattened frontobasal axis. Hislopia prolixa and Echinella placoides often have more slender zooids with a higher frontobasal axis. Apertures of hislopiids are quadrangular, lined by a thickened cuticle. Apertural spines are present in various lengths in E. placoides, Hislopia lacustris and Hislopia corderoi. The remaining cuticle is rather thin except at lateral areas, close to the pore-plates which are prominent in hislopiids because of abundant special and limiting cells. All species except H. corderoi and Timwoodiellina natans have a prominent collar obstructing the vestibulum, whereas the latter two species instead have an 'external collar' as cuticular, outer folds projecting over the aperture. Hislopiid lophophores carry eight, or more commonly 12-18 tentacles. The digestive tract is distinguished by an often highly elongated esophagus and/or cardia, with the latter always having a prominent bulbous part in the form of a proventriculus-or gizzard in E. placoides. The caecum is extensive in all species. In Hislopia the intestine is characteristically two-chambered with a proximal and distal part before entering an anal tube of various length. The latter is present in all species except T. natans and terminates in mid-lophophoral area. Oocytes in E. placoides are large and macrolecithal indicating brooding and the production of lecithotrophic larvae. Hislopia species produce small, oligolecithal ones, which suggests zygote spawning and planktotrophy. In general, the morphology is similar among the different hislopiids with characters of the gut aiding in delineating the genera Echinella and Timwoodiellina.

Phylogenomics reveals deep relationships and diversification within phylactolaemate bryozoans.

Bryozoans are mostly sessile colonial invertebrates that inhabit all kinds of aquatic ecosystems. Extant bryozoan species fall into two clades with one of them, Phylactolaemata, being the only exclusively freshwater clade. Phylogenetic relationships within the class Phylactolaemata have long been controversial owing to their limited distinguishable characteristics that reflect evolutionary relationships. Here, we present the first phylogenomic analysis of Phylactolaemata using transcriptomic data combined with dense taxon sampling of six families to better resolve the interrelationships and to estimate divergence time. Using maximum-likelihood and Bayesian inference approaches, we recovered a robust phylogeny for Phylactolaemata in which the interfamilial relationships are fully resolved. We show Stephanellidae is the sister taxon of all other phylactolaemates and confirm that Lophopodidae represents the second offshoot within the phylactolaemate tree. Plumatella fruticosa clearly falls outside Plumatellidae as previous investigations have suggested, and instead clusters with Pectinatellidae and Cristatellidae as the sister taxon of Fredericellidae. Our results demonstrate that cryptic speciation is very likely in F. sultana and in two species of Plumatella (P. repens and P. casmiana). Divergence time estimates show that Phylactolaemata appeared at the end of the Ediacaran and started to diverge in the Silurian, although confidence intervals were large for most nodes. The radiation of most extant phylactolaemate families occurred mainly in the Palaeogene and Neogene highlighting post-extinction diversification.

Further species and range extensions of Amazonian bryozoans: chipping away at the iceberg.

A bryozoan survey conducted in the Amazon Basin in the vicinities of Manaus and Santarm during the high water season (May, 2018) revealed four new species described here: Fredericella adrianoi n. sp., Plumatella divae n. sp., Plumatella hartikainenae n. sp., and Plumatella spencerjonesae n. sp. Two of these species were encountered only once, suggesting that other undescribed species are likely to occur in the area. Range extensions were determined for two additional species: Plumatella pirassununga and Timwoodiellina natans. In addition, colonies were collected for the first time for two species previously known only by their statoblasts: Plumatella siolii and Plumatella marcusi. Statoblasts of Tapajosella elongata were encountered near Manaus, but the colonies remained elusive. The discovery of new species collected during two expeditions to the Amazon Basin in different seasons and years suggests that further diversity remains undetected in this and other poorly studied regions of the world. With few exceptions, plumatellid colonies described so far from the Amazon Basin are very similar in appearance, with branches wholly attached to the substratum and body walls that are soft, colorless, and transparent.

Phylactolaemate bryozoans at the Zoological Survey of India and a taxonomic key to Indian Phylactolaemata.

A review of the phylactolaemate (freshwater) bryozoan collection at the Zoological Survey of India in Kolkata reaches the following conclusions: (1) Fredericella indica Annandale, 1909 from the Indian subcontinent is not the same as the species widely known as F. indica from the northern temperate zones; the latter species name is now changed to Fredericella borealis; (2) Plumatella bigemmis Annandale, 1919 is a junior synonym of Plumatella fungosa Pallas, 1768; (3) Plumatellia persica Annandale, 1919 is a junior synonym of Plumatella casmiana Oka, 1907; (4) Plumatella (Afrindella) testudinicola Annandale, 1912 combines two previously known species: Plumatella bombayensis Annandale, 1908 and Plumatella casmiana Oka, 1907; (5) Rumarcanella minuta (Toriumi, 1941) is a junior synonym of Stolella himalayana Annandale, 1911 which now becomes Rumarcanella himalayana based on statoblast hypertubercles; (6) Plumatella longigemmis Annandale, 1915 and Hyalinella (Australella) indica Annandale, 1915 are both junior synonyms of Hyalinella lendenfeldi (Ridley, 1886); (7) Stolella indica Annandale, 1909, Swarupella andamanensis Rao, 1961 and Swarupella kasetsartensis Wood, 2006, may all be synonymous. The species Plumatella bombayensis is confirmed, and its holotype is re-described. In addition to Fredericella borealis four new species are presented: Plumatella crispa, P. dhritiae, P. paltensis and P. raoi. Validity is rejected for the genera Afrindella, Australella, Stolella, and Swarupella. The genera Rumarcanella and Varunella require refinement and documentation. A taxonomic key to the Indian Phylactolaemata concludes this paper.

Review of freshwater Bryozoa (Phylactolaemata) of Central Africa with descriptions of two new species.

The Royal Museum of Central Africa at Tervuren, Belgium, includes a small collection of freshwater bryozoans from Congo and Rwanda. Included are: Plumatella philippinensis with both statoblast types, as well as holotypes of Plumatella ruandensis Wiebach, 1964, Plumatella marlieri Wiebach, 1970, and Plumatella pseudostolonata Borg, 1940. There are also two new species which had been previously misidentified: specimens designated as Plumatella javanica are now recognized as P. wiebachi n. sp.; and specimens labeled Stolella indica now recognized as Plumatella kisalensis n. sp. This paper includes full descriptions of the new species as well as fresh descriptions and illustrations of other species in the collection.

Myoanatomy and serotonergic nervous system of the ctenostome Hislopia malayensis: evolutionary trends in bodyplan patterning of ectoprocta.

BACKGROUND: Ectoprocta is a large lophotrochozoan clade of colonial suspension feeders comprising over 5.000 extant species. Their phylogenetic position within the Lophotrochzoa remains controversially discussed, but also the internal relationships of the major ectoproct subclades -Phylactolaemata, Stenolaemata, and Gymnolaemata - remains elusive. To gain more insight into the basic configuration of ectoproct muscle systems for phylogenetic considerations, we analysed the adult myoanatomy and the serotonergic nervous system as well as myogenesis in budding stages of the ctenostome Hislopia malayensis. RESULTS: In adults, the serotonergic nervous system is restricted to the lophophoral base with a high concentration in the cerebral ganglion and serotonergic perikarya between each pair of tentacles. Prominent smooth apertural muscles extend from the basal cystid wall to each lateral side of the vestibular wall. The musculature of the tentacle sheath consists of regular strands of smooth longitudinal muscles. Each tentacle is supplied with two bands of longitudinal muscles that show irregular striation. At the lophophoral base several muscles are present: (i) Short muscle fibres that proximally diverge from a single point from where they split distally into two separate strands. (ii) Proximally of the first group are smooth, longitudinal fibres that extend to the proximal-most side of the lophophoral base. (iii) Smooth muscle fibres, the buccal dilatators, traverse obliquely towards the pharynx, and (iv) a circular ring of smooth muscle fibres situated distally of the buccal dilatators. Retractor muscles are mainly smooth with short distal striated parts. The foregut consists mainly of striated ring musculature with only few longitudinal muscle fibres in the esophagus, while the remaining parts of the digestive tract solely exhibit smooth musculature. During budding, apertural and retractor muscles are first to appear, while the parietal muscles appear at a later stage. CONCLUSIONS: The apertural muscles show high similarity within Ectoprocta and always consist of two sets of muscles. Gymnolaemates and Phylactolaemates show clear differences within their digestive tract musculature, the former showing smooth and longitudinal muscles to a much greater extent than the latter. The complex musculature at the lophophoral base appears promising for inferring phylogenetic relationships, but sufficient comparative data are currently lacking.

Organogenesis during budding and lophophoral morphology of Hislopia malayensis Annandale, 1916 (Bryozoa, Ctenostomata).

BACKGROUND: Bryozoans represent a large lophotrochozoan phylum with controversially discussed phylogenetic position and in group relationships. Developmental processes during the budding of bryozoans are in need for revision. Just recently a study on a phylactolaemate bryozoan gave a comprehensive basis for further comparisons among bryozoans. The aim of this study is to gain more insight into developmental patterns during polypide formation in the budding process of bryozoans. Particular focus is laid upon the lophophore, also its condition in adults. For this purpose we studied organogenesis during budding and lophophoral morphology of the ctenostome bryozoan Hislopia malayensis. RESULTS: Polypide buds develop on the frontal side of the developing cystid as proliferation of the epidermal and peritoneal layer. Early buds develop a lumen bordered by the inner budding layer resulting in the shape of a two-layered sac or vesicle. The hind- and midgut anlagen are first to develop as outpocketing of the prospective anal area. These grow towards the prospective mouth area where a comparatively small invagination marks the formation of the foregut. In between the prospective mouth and anus the ganglion develops as an invagination protruding in between the developing gut loop. Lophophore development starts with two lateral ridges which form tentacles very early. At the lophophoral base, intertentacular pits, previously unknown for ctenostomes, develop. The ganglion develops a circum-oral nerve ring from which the tentacle nerves branch off in adult zooids. Tentacles are innervated by medio-frontal nerves arising directly from the nerve ring, and medio-frontal and abfrontal nerves which originate both from an intertentacular fork. CONCLUSIONS: We are able to show distinct similarities among bryozoans in the formation of the different organ systems: a two-layered vesicle-like early bud, the ganglion forming as an invagination of the epidermal layer in between the prospective mouth and anal area, the digestive tract mainly forming as an outpocketing of the prospective anal area, and the lophophore forming from two lateral anlagen that first fuse on the oral and afterwards on the anal side. Future studies will concentrate on cyclostome budding to complement our knowledge on developmental patterns of bryozoans.

Trapped in freshwater: the internal anatomy of the entoproct Loxosomatoides sirindhornae.

BACKGROUND: Entoprocta is a small phylum of tentacle-bearing spiralian lophotrochozoans that comprises mainly marine representatives, with only two known freshwater species. One of them, Loxosomatoides sirindhornae Wood, 2005 was only recently described, and detailed information on its morphology including adaptations to life in freshwater are unknown. We analyzed the internal anatomy of L. sirindhornae using serial semi-thin sections, 3D reconstruction, as well as immunocytochemistry and confocal laserscanning microscopy. RESULTS: The nephridial system shows high complexity, strikingly similar to that of Urnatella gracilis, the only other known freshwater entoproct. It is composed of 105-120 large flame-bulb terminal organs that occur in the stalk and calyx. In the stalk they terminate in the epidermis, whereas efferent ducts in each terminal organ in the calyx lead to large, paired terminal ducts that fuse close to the central nervous system and open into the atrium by a nephridiopore. Compared to other stolonate entoprocts, L. sirindhornae shows a different stalk-calyx junction by possessing only a single, multicellular canopy instead of a stack of star cells. A sphincter muscle is situated below the diaphragm of the stalk. The remaining musculature is concentrated in the stalk, while the calyx musculature is sparsely developed. The central nervous system is dumbbell-shaped as in basal entoprocts. CONCLUSIONS: The nephridial system probably has mainly osmoregulatory function. Previous studies have shown that L. sirindhornae is unable to cope with higher salinities, suggesting that its adaptation to freshwater has reached such a high degree that it is unable to 'turn off' the nephridial system in higher salinities. The current data available show that the architecture of internal organ systems such as the musculature or the calyx-stalk junction hold more promising information for taxonomic and perhaps even evolutionary inferences in Entoprocta than external characters such as spination. Contrary to previous investigations, the longitudinal calyx musculature of the genus Loxosomatoides should not be classified as generally strong or conspicuous, since its extent and site of insertion differs between species.

Freshwater biodiversity of Guam. 2. First Micronesian record of Plumatella bushnelli Wood, 2001 (Bryozoa, Phylactolaemata).

Plumatella bushnelli Wood, 2001 is the first reported freshwater bryozoan for Micronesia, and the Guam collections are only the fourth record of this species in the world. In Guam it normally occurs as small colonies on the undersides of duckweed leaves but formed larger colonies on artificial substrate.

Ecology, development and pathogenicity of Buddenbrockia plumatellae Schröder, 1910 (Myxozoa, Malacosporea) (syn. Tetracapsula bryozoides) and establishment of Tetracapsuloides n. gen. for Tetracapsula bryosalmonae.

Buddenbrockia plumatellae, an enigmatic worm-like myxozoan, was observed as continuously writhing free and attached 'worms' and as free mature spores in the coelom of the freshwater bryozoans Plumatella fungosa, Hyalinella punctata, and Fredericella sp. 'Worm' numbers could double every three days. 'Worms' and spores could be expelled from colonies by external pressure. Some mature 'worms' exited actively, entraining release of free spores, and gradually ceased movement outside the host. Bryozoans sealed off infected regions of the colony. Infected colonies grew slowly, produced no statoblasts, and eventually regressed and died. Transmission was not achieved and prevalence was low. Electron microscopy of 'worms' revealed a single layer of mural cells on a fibrous basal lamina overlying four longitudinal muscle blocks and an inner sheet of two types of proliferating cells, an organization indicative of the bilaterian ancestry of the Myxozoa. Primary type A cells were attached directly by striated tubules to mural cells at positions between muscle blocks. Secondary type A cells had a secretory function. Type B cells underwent meiosis and subsequently developed to typical malacosporean myxozoan spores filling the internal cavity of the 'worms'. External tubes were formed during capsulogenesis in 'worms' from Fredericella sp. Tetracapsula bryozoides is synonymised with Buddenbrockia plumatellae and a new genus is proposed for Tetracapsula bryosalmonae.