Species of Staurotheca Allman, 1888 (Cnidaria: Hydrozoa: Sertulariidae) from US Antarctic expeditions,with the description of three new species

Seventeen species of the genus Staurotheca Allman have been studied, three of which are new to science (Staurotheca abyssalis sp. nov., S. densa sp. nov. and S. profunda sp. nov.). The material studied was collected by several US Antarctic expeditions. Each species is described and figured, the systematic position amongst allied species discussed and available data concerning autecology and geographical distribution given. The remaining six known species of the genus are also considered, regarding synonymy, autecology and geographical distribution. The type material of two poorly known species of Staurotheca, S. juncea (Vanhöffen) and S. pachyclada (Jäderholm) has been re-examined, re-described and figured. Finally, a general survey of the bathymetrical and biogeographical distribution of the known species of Staurotheca is given.     

Species of Oswaldella Stechow, 1919 (Cnidaria: Hydrozoa: Kirchenpaueriidae) from US Antarctic expeditions,with the description of three new species

Seventeen species of the genus Oswaldella Stechow have been studied, three of which are new to science (Oswaldella frigida sp. nov., O. medeae sp. nov. and O. monomammillata sp. nov.). The material studied was collected by several US Antarctic expeditions. Each species is described and figured, the systematic position amongst allied species is discussed and available data concerning autecology and geographical distribution are given. The remaining eight known species of the genus are also considered, regarding synonymy, autecology and geographical distribution. Finally, a general survey of the bathymetrical and biogeographical distribution of the known species of Oswaldella is given.     

Taxonomic revision and systematic notes on some Halecium species (Cnidaria,Hydrozoa)

Although the genus Halecium is easy to recognize, identifications at the species level are often difficult, this even for quite common and supposedly well‐known species of the north‐eastern Atlantic. This paper revises and re‐describes some Halecium species which resemble each other closely and which are not easy to distinguish. Additional information on a few rare species is also provided. The study is based on material collected from the North Atlantic, Mediterranean, South Africa, and New Zealand. Halecium scutum Clark, is recognized as a valid species and distinct from both H. beanii and H. halecinum; colony form and microscopic characters allow a distinction. The pinnate colony form of H. halecinum is a characteristic trait, but not all colonies show this growth form. Halecium beanii can occur in monosiphonic and polysiphonic colonies. Monosiphonic colonies of H. beanii have probably been misidentified by some authors as H. lankesterii. The differences of H. lankesteri to H. beanii and H. petrosum are discussed. The South African population of the reportedly cosmopolitan H. beanii has distinct gonothecae and could belong to a separate species. The Mediterranean Halecium mediterraneum is hardly distinguishable from the New Zealandic H. delicatulum, but it is kept separate mainly for biogeographic reasons. The rare Mediterranean Halecium banyulense is re‐described based on a second find from Naples. The male gonothecae of Halecium corrugatissimum are described for the first time.     

Redescription and systematic status of the Antarctic genus Abietinella Levinsen, 1913 (Lafoeidae,Hydrozoa, Cnidaria)

The Antarctic–Patagonian genus Abietinella, comprising two known species, Abietinella operculata (Jäderholm, ) and Abietinella grandis (Vanhöffen, ), is reviewed. The holotype of Abietinella operculata is fully redescribed, including morphometry and cnidome, unknown up to now. Its distinctive characters are the growth habit, hydrothecal shape and, most important, the presence of a dish‐shaped operculum attached to the adcauline side of the hydrothecal aperture. We corroborate its conspecificity with A. grandis and, therefore, the monotypic condition of Abietinella.     

Species of Schizotricha Allman, 1883 (Cnidaria: Hydrozoa: Halopterididae) from US Antarctic expeditions with the description of two new species

Twelve species of the genus Schizotricha Allman have been studied, two of which are new to science (Schizotricha heteromera sp. nov. and S. trinematotheca sp. nov.). The material studied was collected by several US Antarctic expeditions. Each new species is described and figured, the systematic position amongst allied species discussed and available data concerning autecology and geographical distribution given. The remaining 10 species are considered regarding diagnosis, autecology and geographical distribution. Finally, a general survey of the bathymetrical and biogeographical distribution of the known species of Schizotricha is given.     

Redescription and life cycle of Eutima sapinhoa Narchi and Hebling, 1975 (Cnidaria: Hydrozoa,Leptothecata): a hydroid commensal with Tivela mactroides (Born) (Mollusca,Bivalvia, Veneridae)

The commensal hydroid Eutima sapinhoa Narchi and Hebling, 1975 Narchi, W and Hebling, N. 1975. The life cycle of the commensal Hydromedusa Eutima sapinhoa n. sp. Marine Biology, 30: 73–78. [Crossref] , [Google Scholar] lives attached to the mantle, gills, labial palps and foot of the bivalve Tivela mactroides. The solitary polyps bud off medusae that become free, leaving the host through the exhalant water current. Newly liberated medusae were cultivated in the laboratory, attaining 7.8?mm in bell height, 13.3?mm in diameter and having eight marginal tentacles, while developing the typical eutimid medusa characters of a long peduncle, four radial canals and marginal statocysts with many statoliths. Eutima sp., previously reported from Florida, USA, is probably referable to Eutima sapinhoa. Like the other bivalve-inhabiting species of Eutima [E. ostrearum (Mattox and Crowell, 1951 Mattox, N. T and Crowell, S. 1951. A new commensal hydroid of the mantle cavity of an oyster. Biological Bulletin, 101: 162–170. [Crossref] , [Google Scholar]) and Eutima sp.] from the Atlantic Ocean, Eutima sapinhoa has no trace of marginal cirri, thereby differing from the eutimid medusae of the Pacific Ocean.     

Morphology and biology of a new Rhynchospio species (Annelida: Spionidae) from the South China Sea,Vietnam, with the review of Rhynchospio taxa

Adults of a new spionid polychaete, Rhynchospio nhatrangi, inhabit sandy tubes on muddy sand intertidal flats in an estuary of Nha Trang Bay, southern Vietnam. The worms are up to 8 mm long and 0.5 mm wide for 55 chaetigers. They are unique among spionids in the changes in the arrangement of hooks during ontogenesis: first development of tridentate hooks in neuropodia from chaetiger 10, later loss of hooks in chaetiger 10, and replacement of tridentate hooks by heavy unidentate hooks in neuropodia of chaetigers 11–14. Adults are simultaneous hermaphrodites having sperm in chaetigers 11–14 and oocytes from chaetiger 15 to 23–33. Spermatozoa are introsperm, about 300 µm long. Oocytes are about 120 µm in diameter, with a thin and smooth envelope. Fertilization and early larval development occur in a hatchery formed by elongated dorsal capillaries on the posterior chaetigers. Larvae escape from the hatchery probably when they have developed four chaetigers and then continue development in seawater, feeding on the plankton. When larvae have grown to 14–15 chaetigers, they likely undergo gradual metamorphosis and settle on the bottom. Metameric nuchal organs, glandular pouches in neuropodia, metanephridial segmental organs, hermaphroditism, sperm, and early larval morphology are described here for the first time for Rhynchospio species. An identification key is provided to eight currently recognized Rhynchospio species.     

A revision of Monocotyle Taschenberg, 1878 (Monogenea: Monocotylidae) with descriptions of three new species from Australia

Monocotyle is revised and three new species are proposed. Monocotyle corali sp. nov. is described from the gills of the cowtail ray, Pastinachus sephen (Forsskål) (Dasyatididae), and is distinguished from other members of Monocotyle by the large hamuli with a distinct tail on the guard and by the male copulatory organ with three loops and a wing-like accessory piece at the distal end. Monocotyle jordani sp. nov. from the gills of the southern eagle ray, Myliobatis australis Macleay (Myliobatididae), is differentiated by the male copulatory organ with a large, unique accessory piece. Monocotyle youngi sp. nov., from the gills of Himantura fai Jordan and Seale (Dasyatididae), has marginal haptoral papillae armed with 12 to 15 sclerites, a male copulatory organ with 20 loops and a unique accessory piece at the distal end. Monocotyle trygoni (Venkatanarsaiah and Kulkarni, 1980) Timofeeva, 1985 is synonymized with M. spirophallus Tripathi, 1959 and M. spirophallus is redescribed fully. There are now 16 valid species of Monocotyle and a key to species is presented. Additional data and illustrations of important taxonomic characters are provided. The developmental sequence of the male copulatory organ of M. spiremae Measures, Beverley-Burton and Williams, 1990 from juvenile to adult is described. The anterior glands and the type of secretion they contain are also documented for several species of Monocotyle.     

Reproduction,phenology and mortality sources of a species of Physalaemus (Anura: Leptodactylidae)

Physalaemus cf. fuscomaculatus is a foam-nesting frog of seasonally dry environments of south-eastern Brazil. We report on the reproduction and other natural history features of this species. Population parameters were based on trapped specimens. The advertisement call is described. The calling and spawning season is coincident with the rainy period. Calling and spawning were performed in ponds. Most of the adults were trapped in October and the juveniles during wetter months and the beginning of the dry season. At the end of the reproductive season, the median size of adults lowered. Egg clutches averaged 2350 eggs, each egg being about 1.4?mm in diameter. Males were more abundant than females in traps. Communal foam nests were frequent, involving up to 40 individual nests. Tadpoles entered the water within about 40?h. Maggots (Diptera) infested egg clutches; water bugs and mammals preyed upon adults. In this region, the dry/cold season may be so difficult for survival that early maturation at small size would be advantageous. The male-biased sample may be related to the greater motility of males. The rapid abandonment of the foam by the tadpoles and communal nesting may help to reduce predation by maggots. Skin toxins were not effective in deterring predation upon adults. The call of P. cf. fuscomaculatus differs from that of other species in the biligonigerus group and can help to define the specific status of the studied population.     

Similiclava nivea (Cnidaria: Hydrozoa: Similiclavidae): a new family,genus and species of athecate hydroid from the Pacific coast of North America

The hydroid Similiclava nivea, gen. nov., sp. nov., is described from colonies collected in nearshore waters of southern British Columbia, Canada. It has been observed by divers, and recorded as Clava sp., several hundred times at locations between southeast Alaska and southern Oregon, USA. While resembling the hydractiniid Clava multicornis, tentacles of S. nivea are arranged in two close whorls in extended hydranths rather than being scattered over the distal end of the hydranth. Moreover, the hypostome is dome-shaped to flattened instead of being proboscidiform. Similiclava nivea also resembles species of the hydractiniid genera Stylactaria, Hydractinia and Podocoryna, but differs in being monomorphic, in lacking spines on the hydrorhiza and in having numerous (as many as 50 or more) sporosacs borne in a broad whorl below the tentacles on normal hydranths. Molecular analysis using the mitochondrial 16S gene sequences reveals that S. nivea is closer to Clathrozoellidae than to Hydractiniidae, although it is clearly distinct from both. A new family, Similiclavidae, is established to accommodate the species. Hydroids of S. nivea were observed at relatively shallow depths (10–30 m) on rocks and epibiota attached to rocky substrates. Colonies are conspicuous because of the relatively large surface area they occupy (up to 20 cm across, and in aggregations often exceeding 100 or more hydranths) together with the height (about 15 mm high when extended) and striking white colour of living hydranths. The cnidome consists of desmonemes, microbasic euryteles and microbasic mastigophores. A substrate generalist observed on rocks, algae, sponges, barnacles, bryozoans and other hydroids in cold-temperate waters, S. nivea is most prevalent in shallow subtidal areas swept by tidal currents.

http://zoobank.org/urn:lsid:zoobank.org:pub:2691E02E-7E14-4820-8D91-41D9E7E8BF62     

Reproductive ecology and behaviour of a species of Adenomera (Anura,Leptodactylinae) with endotrophic tadpoles: Systematic implications

The species of the Leptodactylus fuscus group and those of the genus Adenomera lay their eggs in underground chambers. According to current systematic arrangement of these genera, this behaviour is convergent. Here we describe reproduction, courtship, tadpole morphology, calls, chamber structure, and populational phenology of an Adenomera species, and compare some of these features with those of other species of the genus and with species of Leptodactylus of the fuscus and pentadactylus groups. We tested the tadpoles of the Adenomera sp. and those of Leptodactylus labyrinthicus (pentadactylus group) for their foam‐making abilities. There was sexual dimorphism in size; males averaged 22.0?mm and females 24.3?mm in snout–vent length. Males called from late September to late February; calling often began about 2–3?h before sunset. Males called exclusively in open (non‐forest) areas. Egg clutches were found around male calling sites. Males excavated spherical chambers which had a direct entrance. During mating, the male led the female towards a previously excavated chamber. Territorial interactions (aggressive calls and fights) occurred when an intruder male approached a calling male. Late‐stage tadpoles and newly metamorphosed juveniles were found within underground chambers. Clutch size averaged 10.6; eggs averaged 3.7?mm in diameter and were cream coloured. Tadpoles had horny beaks, but no labial tooth; spiracle was present. All tested groups of tadpoles generated foam within 10?h. As we report for Adenomera sp., the males of Leptodactylus species of the fuscus group lead the female to a previously excavated chamber. Tadpole foam‐making behaviour was reported in Leptodactylus of the fuscus group and was previously unknown for any species of Adenomera or for Leptodactylus of the pentadactylus group. The way in which the tadpoles of Adenomera sp., Leptodactylus spp. (of the fuscus group) and L. labyrinthicus made foam was quite similar. The foam‐making behaviour of the studied tadpoles may act to avoid compaction of the tadpoles at the bottom of the basin or underground chamber, avoiding overcrowding and increasing respiratory and excretory efficiency. As presently recognized, the phylogenetic position of Adenomera suggests that reproductive major behavioural features are convergent with some Leptodactylus species. Alternatively, our data point to close phylogenetic relationships between Adenomera and Leptodactylus of the fuscus and pentadactylus groups, reinforcing the paraphyletic nature of the genus Leptodactylus.     

Five new species of Monocelis Ehrenberg, 1831 (Platyhelminthes: Proseriata) from eastern Australia

Six species of the genus Monocelis Ehrenberg, 1831 have been found in eastern Australia. All are new to science. Five of them are formally described here. Three species (M. rupisrubrae sp. nov., M. nexilis sp. nov., and M. corallicola sp. nov.) have two clearly set pigmented eyespots lateral to the statocyst. They differ in details of the copulatory organ and karyotype. No clear synapomorphies among them or with other species of the genus could be detected. Monocelis beata sp. nov. and M. macrobulbus sp. nov. present extremely elongate, longitudinally oriented copulatory organs. They are sister species, and phylogenetic relationships with M. galapagoensis Ax and Ax, 1977 and M. hopkinsi Karling, 1966 are proposed. Australian Monocelis have distributions limited to recognized biogeographical provinces in eastern Australia: M. corallicola, M. beata and M. macrobulbus in the northern Australian Zone, M. rupisrubrae and M. nexilis in the ‘Overlap Zone’ of the central east coast and Monocelis sp. A in the southern Australian Region.     

Biometry of brooding in seven species of amphipod (Crustacea) from the Clyde Sea area

Brood size was found to be correlated linearly with female body length in all species studied, except Ampelisca macrocephala, which is usually a single brooded species. Of the six multi-brooded species, Lembos websteri, Stegocephaloides christianiensis, Echinogammarus pirloti and Gammaropsis nitida produced small numbers of large eggs in the winter and large numbers of small eggs in the summer. In Bathyporeia pilosa larger numbers of smaller eggs were produced by the overwintering generation. In Corophium bonnellii, both maximum and minimum brood sizes were produced by the summer generation. The largest broods relative to female body size were produced by the smaller species. In L. websteri, C. bonnellii and B. pilosa mean female size was smaller in the summer than the winter generation.     

Analysis of teeth outlines: a morphometric tool for distinguishing three species of Crocidurinae (Soricidae,Insectivora, Mammalia) in France

Crocidurinae (Soricidae, Insectivora) are represented by many present-day species which are morphologically very similar. The efficiency of morphometric analyses in the discrimination between species has already been proved for various organisms, and the discriminant model developed here is based on the analysis of teeth outlines in three living species, Crocidura leucodon, Crocidura suaveolens and Crocidura russula, using the Fourier transform method. The application of this method on the upper and lower premolars and molars permits the three species to be clearly separated, and the model can be used for the identification of fossils.     

Larval development of Apiomithrax violaceus (A. Milne Edwards, 1868) (Decapoda: Brachyura: Majoidea: Pisidae) reared in laboratory conditions,and a review of larval characters of Pisidae

Apiomithrax violaceus (A. Milne Edwards, 1868 Milne Edwards A 1868 Observations sur la faune carcinologique des Iles du Cap-Vert Nouvelles Archives du Muséum d'Histoire Naturelle, 4, 49–68, pls 16–18  [Google Scholar]) is a pisid majoid crab occurring in tropical and subtropical coastal waters of the eastern and western South Atlantic. Larval development consists of two zoeal stages and a megalopa. Beginning with the first zoea, the duration of each larval stage at 24°C was 3–8 (5±1), 3–5 (4±0.5) and 9–15 (11±2) days, the megalopa and first crab instar appearing 9–11 (10±1) and 20–27 (23±2) days after hatching, respectively. Larval characters agree with those proposed for the Majoidea, in having nine or more setae on the scaphognathite in the first zoea and well-developed pleopods in the second zoea. However, larvae of A. violaceus do not fit larval pisid features. Zoeal stages differ from most other Pisidae in having lateral spines, a long rostral spine extending beyond the antenna, two spines per telson fork and a dorsolateral process on the third abdominal somite. The megalopa differs in having a spine dorsally on the carapace and on the basial segment of the second pereiopod. Two characters that are potentially unique to Apiomithrax include a zoeal antenna with an exopod that is much longer than the protopod, and a rostral spine that is longer than the dorsal spine. These characters should facilitate the identification of this taxon and could also be useful for phylogenetic studies. A review of larvae of 28 species among 14 genera indicated that there is no apparent single larval character that differentiates the Pisidae, with more limited phylogenetic analyses suggesting that this is a paraphyletic group. Apiomithrax, Eurynolambrus, Pisoides, Rochinia and Scyra have the most divergent morphological characters within the family. The analysis and inclusion of additional taxa is likely to shed more light on the sister-group relationships of the Pisidae. However, based on the extent of morphological interspecific variability of known larvae it is likely that the group, as presently defined by adult morphology, is not monophyletic.     

Species of Symplectoscyphus Marktanner-Turneretscher, 1890 (Cnidaria: Hydrozoa,Sertulariidae) from recent Antarctic expeditions with R.V. Polarstern,with the description of four new species

Fifteen species of the genus Symplectoscyphus Marktanner-Turneretscher have been studied, four of which are new to science (Symplectoscyphus anae sp. nov., S. frigidus sp. nov., S. sofiae sp. nov. and S. weddelli sp. nov.). The material studied originates from the Weddell Sea and was collected by several French and German Antarctic expeditions with R.V. Polarstern. Each species is described and figured, the systematic position amongst allied species discussed and available data concerning autecology and geographical distribution given. The type material of five poorly known species of Symplectoscyphus, S. aggregatus (Jäderholm), S. cumberlandicus (Jäderholm), S. glacialis (Jäderholm), S. hero Blanco and S. plectilis (Hickson and Gravely), has been re-examined, re-described and figured. Finally, a general survey of the bathymetrical and biogeographical distribution of the known Antarctic species is given.     

Coexistence of species of two amphipod genera: Niphargus timavi (Niphargidae) and Gammarus fossarum (Gammaridae)

The co‐occurrence of amphipods Niphargus timavi and Gammarus fossarum was studied. A small brook in SW Slovenia was sampled monthly for one year. Below the primary spring the brook sinks, flows for about 150 m below the surface and springs again. Gammarus fossarum never reached the stretch above the sink. Both species were found at all sampling sites below the secondary spring throughout the year, but the abundance of the two varied along the stream spatially and temporarily. Differences in life cycles between G. fossarum and N. timavi were not informative; however, the estimated reproductive potential of G. fossarum was much higher than of N. timavi. A result of the higher reproductive potential may be the dominance of gammarids in permanent waters, while N. timavi may invade a surrounding fissure system where it survives gammarid competition and summer desiccations when the gammarid population becomes extinct.