A new species of hagfish (Myxinidae: Eptatretus) from Papua New Guinea

A new species of seven‐gilled hagfish Eptatretus astrolabium (Myxinidae) is described from a 400 mm total length female trapped 1 km east from Planet Rock, Astrolabe Bay, Papua New Guinea, at c. 500 m depth. This is the first hagfish species reported from the waters around New Guinea. It can be distinguished from other hagfishes by a combination of characters including seven pairs of gill apertures, three‐cusp multicusps on the anterior and posterior rows of cusps, 10 posterior unicusps, 52 total cusps, 18–19 prebranchial pores, five branchial pores, 48–49 trunk pores, 83–84 total pores and no nasal‐sinus papillae.     

Redescription of the hagfishes (Myxinidae: Eptatretus) from southern Africa

The hagfishes of the genus Eptatretus (Myxinidae) from southern Africa are known from three poorly studied species: Eptatretus hexatrema, a common species from Namibia and South Africa; Eptatretus profundus, known only from the holotype collected off Cape Point (South Africa); and Eptatretus octatrema, known from two syntypes from the Agulhas Bank (South Africa). Taxonomic, morphological and distributional information about these three species are reviewed and updated based on the examination of additional specimens collected in South African waters. Eptatretus hexatrema differs from all congeners by having six pairs (rarely seven) of gill apertures arranged in a straight line, 3/2 multicusp pattern of teeth, total cusps 44–49, trunk pores 53–60, total pores 93–107, preventral length 45.1–57.4% TL, tail length 11.6–14.3% TL, tail depth 5.7–8.1% TL, and two bilaterally symmetrical nasal-sinus papillae. Eptatretus octatrema differs from all congeners by having usually eight (some specimens with seven) pairs of gill apertures arranged in a straight line, 3/2 multicusp pattern of teeth, 42–46 total cusps, 22–26 prebranchial pores, 63–68 trunk pores, 104–117 total pores, and two bilaterally symmetrical nasal-sinus papillae. Eptatretus profundus differs from all congeners by having five pairs of gill apertures arranged in a straight line, 3/2 multicusp pattern of teeth, total cusps 42–46, prebranchial pores 12–15, branchial pores 4–5, trunk pores 48–52, tail pores 15–17, total pores 81–86, and body depth at PCD 7.0–9.7% TL. An identification key for the hagfishes from southern Africa is provided and the conservation status of E. octatrema, a species considered to be Critically Endangered, is discussed in light of the new findings.     

Eptatretus strickrotti n. sp. (Myxinidae): first hagfish captured from a hydrothermal vent

A single hagfish (Myxinidae, Eptatretus) specimen was recently captured at a hydrothermal vent site on the East Pacific Rise (38 degrees S). This is the first capture of a member of the jawless fishes (agnathans) from a hydrothermal vent site. The specimen differs from all congeners by the very slender body (depth 2.9% of total length), the paired and median ventral nasal sinus papillae, and the presence of 10 afferent branchial arteries on the medial ventral aorta. It is further unique because of a combination of the following features: slime pore counts; paired dorsal nasal sinus papillae; 12 gill pouches and gill apertures; posterior left side of body widely separated from pharyngocutaneous duct; 3/2 multicusp configuration; ventral aorta bifurcated anteriorly between 2nd and 3rd gill pouches (counted from the snout toward the heart); and pink coloration. The specimen is here described as a new species named Eptatretus strickrotti. Molecular 16S rRNA data places this new species as the basal-most species of Eptatretus, providing important new insight to the evolution of hagfishes as a whole.     

A new species of Odontostilbe cope (Characiformes: Cheirodontinae) from rio Madeira basin diagnosed based on morphological and molecular data

A new species of Odontostilbe is described from the rio Jaciparaná, rio Madeira basin, Rondônia, Brazil. Odontostilbe pacaasnovos differs from all its congeners, except O. pequira, by the colour pattern. Additionally, it differs from its congeners by the terminal mouth, number of cusps in the teeth of the premaxilla (5–7), number of branched rays in the anal fin (19–22), by the shape of dentary teeth (5–7 cusps with central cusp larger and longer than laterals cusps) and by the number of lamellae of the olfactory rosette (17–18 in male and 14 in female). Morphological and molecular comparisons corroborate the distinctiveness between O. pacaasnovos and its congeners, justifying its recognition as a new species.     

Description of a new species of Triplophysa (Teleostei: Nemacheilidae) from Guizhou Province,China

A new cave‐dwelling fish species Triplophysa guizhouensis is described based on specimens collected from Guizhou, China, in a subterranean system interconnected with the Hongshui River drainage. The species can be distinguished from its congeners by a combination of characters: eyes present; caudal fin with 14 branched rays; inner gill rakers of first gill arch 8–10; posterior chamber of air bladder developed; and body posterior of dorsal fin scaled. A key to species of Triplophysa in the Pearl River basin is provided.     

Hagfish phylogeny and taxonomy,with description of the new genus Rubicundus (Craniata,Myxinidae)

A recent phylogenetic analysis of the Myxinidae based on the 16S rRNA gene resulted in synonymization of Paramyxine with Eptatretus. This created homonymy of Paramyxine fernholmi with Eptatretus fernholmi and Paramyxine wisneri with Eptatretus wisneri. In order to resolve this nomenclatural dilemma, we made a more extensive phylogenetic assessment of the Myxinidae and examined the nomenclature of the family. We used 75 sequences (37 of which new for this study) of a 561 bp fragment of the 16S rRNA gene, representing 33 species, and 72 sequences (37 of which new for this study) of a 687 bp fragment of the cytochrome c oxidase subunit I (COI) gene, representing 23 species, to reconstruct the phylogeny of Myxinidae. The monophyly of the subfamily Myxininae, traditionally characterized by having a single pair of external gill openings, was rejected (0.50 Bayesian posterior probability) by the 16S analysis, but supported by the COI and combined COI+16S analyses (0.99 and 0.81 Bpp, respectively). The monophyly of the subfamily Eptatretinae, characterized by having several pairs of external gill openings, was not supported by the 16S analysis and rejected by the COI and combined COI+16S analysis due to the placement of Eptatretus lopheliae as the earliest branch of Myxinidae (0.71 and 0.57 Bpp, respectively). Eptatretus lopheliae and Eptatretus rubicundus formed a monophyletic group and were allocated to a new genus, Rubicundus, characterized by the presence of an elongated tubular nostril and reddish coloration. A new monotypic subfamily, Rubicundinae, was proposed for Rubicundus. The synonymy of the genera Paramyxine and Quadratus with Eptatretus was confirmed. E. fernholmi is renamed Eptatretus luzonicus. Eptatretus wisneri was renamed Eptatretus bobwisneri. Petromyzon cirrhatus Forster, 1801, Homea banksii Fleming, 1822, and Bdellostoma forsteri Müller, 1836 are synonyms, but no type specimens are known to exist. Petromyzon cirrhatus was designated as type species of Eptatretus, conserving present usage. Gastrobranchus dombeyi Shaw, 1804 has priority over other names for Chilean myxinids. Bdellostoma stoutii was designated as type species of Polistotrema Gill. The validity of the Western Atlantic Myxine limosa as distinct from the Eastern Atlantic Myxine glutinosa was confirmed.     

The Different Vascular Patterns of Slime Glands in the Hagfishes,Myxine glutinosa Linnaeus and Eptatretus stouti Lockington A Scanning Electron Microscope Study of Vascular Corrosion Casts*

The vascular patterns of the epidermally derived slime glands of the Atlantic hagfish, Myxine glutinosa, and of the Pacific hagfish, Eptatretus stouti, have been studied by scanning electron microscopy of vascular corrosion casts. In Myxine a simple two-dimensional vascular network sheaths the slime glands, while in Eptatretus there is also a great number of capillary loops of different lengths arising from the sheathing network and extending into the interior of the glands. These basic differences in slime glands vascular patterns are thought to reflect substantially different physiological behaviour of the slime glands in Myxine and Eptatretus.     

Triplophysa ferganaensis,a new loach species from Fergana Valley in Central Asia (Teleostei: Nemacheilidae)

Triplophysa ferganaensis sp. nov. is described from the Shakhimardan stream, a small tributary of the Syr Darya, which does not reach the river in Fergana Valley. It can be distinguished from other valid Triplophysa loaches based on the following combination of characters: body smooth and scaleless, lateral line complete, posterior chamber of air bladder degenerated, inner gill rakers 10–11 on the first-gill arch, outer gill rakers absent, vertebrae 4 + 35–36, 8 + 8 branched caudal-fin rays, caudal peduncle depth 2.1–2.7 times its length, two supratemporal pores, dorsal-fin origin closer to the caudal-fin base than to the snout tip, caudal fin emarginated and pelvic-fin tip reaching the anus. The new species can also be distinguished from its congeners based on the molecular analyses of mitochondrial cytochrome oxidase subunit I (coI) gene sequences. The phylogenetic position of this new species indicates that it is a sister taxon of Triplophysa tenuis.     

The filter pads and filtration mechanisms of the devil rays: Variation at macro and microscopic scales

Three lineages of cartilaginous fishes have independently evolved filter feeding (Lamniformes: Megachasma and Cetorhinus, Orectolobiformes: Rhincodon, and Mobulidae: Manta and Mobula); and the structure of the branchial filters is different in each group. The filter in Rhincodon typus has been described; species within the Lamniformes have simple filamentous filters, but the anatomy and ultrastructure of the branchial filter in the mobulid rays varies and is of functional interest. In most fishes, branchial gill rakers are elongated structures located along the anterior ceratobranchial and/or epibranchial arches; however, mobulid gill rakers are highly modified, flattened, lobe‐like structures located on the anterior and posterior epibranchial elements as well as the ceratobranchials. The ultrastructure of the filter lobes can be smooth or covered by a layer of microcilia, and some are denticulated along the dorsal and ventral lobe surface. Flow through the mobulid oropharyngeal cavity differs from other filter‐feeding fishes in that water must rapidly deviate from the free stream direction. There is an abrupt 90° turn from the initial inflowing path to move through the laterally directed branchial filter pores, over the gill tissue, and out the ventrally located gill slits. The deviation in the flow must result in tangential shearing stress across the filter surface. This implies that mobulids can use cross‐flow filtration in which this shearing force serves as a mechanism to resuspend food particles initially caught by sieving or another capture mode. These particles will be transported by the cross filter flow toward the esophagus. We propose that species with cilia on the rakers augment the shear mediated movement of particles along the filter with ciliary transport. J. Morphol. 274:1026–1043, 2013. © 2013 Wiley Periodicals, Inc.     

The morphology and vasculature of the lungs and gills of the soldier crab,Mictyris longicarpus

The five gill pairs of Mictyris longicarpus have the lowest weight specific area reported for any crab. The cuticle of the gill lamellae is lined with epithelial cells which have structural features characteristic of iontransporting cells. Pillar cells are regularly distributed in the epithelium and serve to maintain separation of the two faces of the lamellae. The central hemolymph space is divided into two sheets by a fenestrated septum of connective tissue cells. The dorsal portion of the marginal canal of each lamella receives hemolymph from the afferent branchial vessel and distributes it to the lamella while the ventral portion of the canal collects hemolymph and returns it to the efferent branchial vessel. The lung is formed from the inner lining of the branchiostegite and an outgrowth of this, the epibranchial membrane. Surface area is increased by invagination of the lining which forms branching, blind-ending pores, giving the lung a spongy appearance. The cuticle lining the lung is thin and the underlyng epithelial cells are extremely attenuated, giving a total hemolymph/gas distance of 90–475 nm. Venous hemolymph is directed close to the gas exchange surface by specialised connective tissue cells and by thin strands of connective tissue which run parallel to the cuticle. Air sacs are anchored in position by paired pillar cells filled with microtubules. Afferent hemolymph is supplied from the eye sinus, dorsal sinus, and ventral sinus. Afferent vessels interdigitate closely with efferent vessels just beneath the respiratory membrane. The two systems are connected by a “perpendicular system” which ramifies between the airways and emerges to form a sinus beneath the carapace and then flows back between the air sacs to the efferent vessels. The afferent side of the perpendicular system is the major site of gas exchange. Efferent vessels return via large pulmonary veins to the pericardial cavity. P_aO₂ levels were high (95.5 Torr), indicating highly efficient gas exchange.     

Genetic integration of molar cusp size variation in baboons

Many studies of primate diversity and evolution rely on dental morphology for insight into diet, behavior, and phylogenetic relationships. Consequently, variation in molar cusp size has increasingly become a phenotype of interest. In 2007 we published a quantitative genetic analysis of mandibular molar cusp size variation in baboons. Those results provided more questions than answers, as the pattern of genetic integration did not fit predictions from odontogenesis. To follow up, we expanded our study to include data from the maxillary molar cusps. Here we report on these later analyses, as well as inter‐arch comparisons with the mandibular data. We analyzed variation in two‐dimensional maxillary molar cusp size using data collected from a captive pedigreed breeding colony of baboons, Papio hamadryas, housed at the Southwest National Primate Research Center. These analyses show that variation in maxillary molar cusp size is heritable and sexually dimorphic. We also estimated additive genetic correlations between cusps on the same crown, homologous cusps along the tooth row, and maxillary and mandibular cusps. The pattern for maxillary molars yields genetic correlations of one between the paracone–metacone and protocone–hypocone. Bivariate analyses of cuspal homologues on adjacent teeth yield correlations that are high or not significantly different from one. Between dental arcades, the nonoccluding cusps consistently yield high genetic correlations, especially the metaconid–paracone and metaconid–metacone. This pattern of genetic correlation does not immediately accord with the pattern of development and/or calcification, however these results do follow predictions that can be made from the evolutionary history of the tribosphenic molar. Am J Phys Anthropol, 2010. © 2009 Wiley‐Liss, Inc.     

A new species of anchovy,Encrasicholina auster (Clupeiformes: Engraulidae) from Fiji,southwestern Pacific Ocean

ABSTRACT

Encrasicholina auster sp. nov. (Clupeiformes: Engraulidae) is described on the basis of six specimens collected from Fiji, southwestern Pacific Ocean. The new species is distinguished from congeners by the following combination of characters: long upper jaw (posterior tip extending beyond posterior margin of preopercle) 20.8%–22.5% standard length (SL); long lower jaw 19.0%–20.7% SL; long head 29.1%–29.2% SL; three unbranched rays in the dorsal and anal fins; transverse scales 11; branched pectoral-fin rays 12–13; pseudobranchial filaments 19–21; gill rakers 45–49, 40–43, 26–31 and 22–25 on the first, second, third and fourth gill arches, respectively.     

A scanning electron microscope study of Craspedella sp. from the branchial chamber of redclaw crayfish,Cherax quadricarinatus,from Queensland,Australia

Epidermal topography was examined, including papillate ridges, grooves and ciliated sensory papillae of Craspedella sp. from the branchial chamber of redclaw crayfish, Cherax quadricarinatus, from Queensland, Australia. Rhandites were observed to discharge from ducts opening mainly in a small distal region of the ventral epidermis of the three central (of five) tentacles. These regions, devoid of ciliated sensory papillae, serve to adhere the anterior end of the worms during locomotion. Secretions from glands associated with the posterior attachment organ were observed to discharge from pores on the outside region of the ventral surface of the disc.A comparison of various scanning electron microscopy (SEM) fixation techniques showed that (1) hot fixatives at 90 °C provide most information on the largest number of epidermal structures and (2) different fixation regimes highlight different epidermal features.     

Description of a new snake eel,Apterichtus hatookai sp. nov. (Anguilliformes: Ophichthidae), from the Pacific coast of Japan

A new species of snake eel (family Ophichthidae, subfamily Ophichthinae), Apterichtus hatookai, is described based on the 478.5 mm holotype and three paratypes, 265.0–519.4 mm in total length (TL), collected from the Pacific Ocean, off the coasts of Shikoku Island and central Honshu Island, Japan. The new species can be distinguished from its congeners, except for Apterichtus monodi and Apterichtus orientalis, by having seven supratemporal pores. The new species is distinguishable from A. monodi by having a longer tail (60.4–62.0 % TL vs. 57.4–60.2 %), four preopercular pores (vs. three), fewer lateral-line pores before the anus (54–58 vs. 63–68), and fewer total vertebrae (137–141 vs. 142–151). Apterichtus hatookai differs from A. orientalis in having a shorter head (5.1–6.1 % TL vs. 7.1–8.1 %; 13.3–16.0 % of preanal length vs. 16.2–18.0 %), a longer tail (60.4–62.0 % TL vs. 54.8–56.0 %), lower body depth at gill opening (0.9–1.5 % TL vs. 1.8–1.9; 2.3–3.8 % of preanal length vs. 4.1–4.2 %), more numerous total vertebrae (137–141 vs. 131–133), and by the anterior tip of the lower jaw below the center of the eye (vs. anterior to a vertical through anterior margin of eye).     

Balitora eddsi,a new species of hillstream loach (Ostariophysi: Balitoridae) from Nepal

A new species of hillstream loach Balitora eddsi is described from the Karnali River drainage in south‐western Nepal. The new species is distinguished from all its congeners by possessing the following combination of characters: six to seven unbranched pectoral‐fin rays, pelvic‐fin length 12–14% standard length (L_S), dorsal surface without circular or irregular shaped dark blotches, snout pointed, median lobe between anterior rostral barbels pointed posteriorly, dorsal‐fin origin posterior to pelvic‐fin origin, lateral line scales 66–67, caudal peduncle length 22–23·2% L_S, caudal peduncle depth 4·1–4·2 times its length.     

Review and phylogeny of the New Zealand hagfishes (Myxiniformes: Myxinidae), with a description of three new species

Hagfishes from New Zealand are reviewed and a phylogeny proposed using morphological and genetic data (DNA sequences of cytochrome c oxidase subunit I gene, COI, and the small subunit RNA, 16S). E ptatretus cryptus sp. nov. was previously confused with Eptatretus cirrhatus (Forster in Bloch & Schneider, 1801) because of their similar morphology, and is found from the Three Kings Islands to Stewart Island and in the eastern part of the Chatham Rise (at depths of 96–922 m). E ptatretus poicilus sp. nov. is endemic to the Three Kings Islands, where it is common and associated with soft sediment and deep‐sea coral‐sponge habitats (114–842 m). N eomyxine caesiovitta sp. nov. is a slender hagfish found along the east coast of the North Island south to the Chatham Rise (430–1083 m). A neotype is erected for E. cirrhatus (type locality: Breaksea Sound, Fiordland), occurring widely in New Zealand coastal, shelf, and slope waters (1–922 m), but not at the Three Kings Islands. Eptatetrus goliath Mincarone & Stewart, 2006, Neomyxine biniplicata (Richardson & Jowett, 1951), and Nemamyxine elongata Richardson, 1958 are further described using additional material. Rubicundus eos (Fernholm, 1991) is still only known from the holotype (type locality: Challenger Plateau). Genetic results showed that the New Zealand Eptatretus species form a monophyletic group within the subfamily Eptatretinae, indicating likely speciation from a single common ancestor within the area. E ptatretus poicilus sp. nov. is the sister species of E. cirrhatus, and E . cryptus sp. nov. is closely associated with the clade formed by these two species. Eptatretus goliath is most closely associated with Eptatretus minor Fernholm & Hubbs, 1981 (Gulf of Mexico), these two species basally diverging within New Zealand hagfishes. The endemic genus Neomyxine forms a well‐supported monophyletic group of as yet uncertain position within the phylogenetic tree. A key to the New Zealand hagfishes, fresh colour photographs, distribution maps, and in situ video recordings are presented. © 2015 The Linnean Society of London     

Gill area and dimensions of gilthead sea bream Sparus aurata L.

Detailed measurements of gill area and constituent variables (total filament length, lamellar frequency and bilateral area) were performed on both hemibranchs of all eight arches in six specimens of gilthead sea bream Sparus aurata (mean ±s.e . 49·9 ± 0·2 g). Shrinkage was also quantified and results were corrected accordingly. Filament number decreased from the first to the fourth gill arch, and average bilateral area of secondary lamellae was higher in the second and third arches. Total and mean filament length, total number of secondary lamellae and total gill area (A_TG) were lower in posterior than in anterior hemibranchs of the second, third and fourth gill arches; while the opposite was observed for the first arch. Lamellar frequency was increased in posterior hemibranchs of all arches compared to that in anterior hemibranchs, especially at the fourth arch. Comparison of the actually measured A_TG and constituent variables with estimates revealed that the third gill arch is the most representative for appropriate measurements and that any of its components (even one hemibranch) approximates the best A_TG (within the range of 0·2–4·3%, P > 0·05) and related dimensions. Consequently, necessary measurements were restricted to the posterior hemibranch of the third gill arch, and A_TG and dimensions (y) were estimated in 21 specimens (23·5–217·6 g) and correlated to body mass (M) according to the allometric equation y = aM^b. As fish increased in size, A_TG (b= 0·664), total (b= 0·425) and mean (b= 0·323) filament length, total number of filaments (b= 0·103) and secondary lamellae (b= 0·377), as well as average lamellar bilateral area (b= 0·288), increased, while the opposite was observed for lamellar frequency (b=?0·049) and mass‐specific area (b=?0·336). Data obtained are discussed in relation to S. aurata activity and living ethology.     

Structure of the ovary and mode of oogenesis in a freshwater crab Potamon dehaani

Structure of the adult ovary and oogenetic mode were examined in the freshwater crab Potamon dehaani. An H‐shaped ovary consisting of a pair of long ovarian sacs connected by a narrow bridge tube is located in the cephalothorax on the dorsal side of the stomach. A short oviduct with a seminal receptacle is connected with the posterior end of each ovarian sac, and a genital pore opens on the sternum of the sixth thoracic segment. The ovarian wall consists of a layer of ovarian epithelium that infolds to form a number of oogenetic pouches of various sizes. These are present mainly in the anterior regions of the ovarian sacs, are scarce in the posterior regions of the ovarian sacs, and are absent from the bridge tube. Each oogenetic pouch contains an egg or a relative large oocyte in its lumen. Germaria containing oogonia, very early previtellogenic oocytes, and somatic interstitial cells are located in the ovarian epithelium near the necks of the oogenetic pouches in the anterior regions of the ovarian sacs and are randomly scattered throughout the ovarian epithelium in the posterior regions of the ovarian sacs. In cross section, the germaria appear to be concentrated into a central germarial cluster in the ovarian sac. In the posterior regions of the ovarian sacs, however, the germaria are randomly scattered throughout the ovarian epithelium. An early previtellogenic oocyte leaves its germarium and raises the ovarian epithelium infolds to form a new oogenetic pouch in which it grows to maturity. Mature eggs are ovulated from the oogenetic pouches into the ovarian lumen, transferred from the ovarian lumen into the oviducts, fertilized there by sperm stored in the seminal receptacles, and then oviposited through the genital pores. The female reproductive system is surrounded wholly and tightly by a thin, cellular, membranous sheath, which has often been mistaken as the ovarian epithelium in some decapod crustaceans. J. Morphol. 239:107–114, 1999. © 1999 Wiley‐Liss, Inc.     

Validity of the atherinid fish, Atherinomorus vaigiensis (Quoy and Gaimard, 1825), with comments on its synonymy

The Australian marine atherinid fish, Atherinomorus vaigiensis (Quoy and Gaimard, 1825), having long been synonymized under A. lacunosus (Forster in Bloch and Schneider, 1801), is redescribed as a valid species based on the holotype and non-type specimens. Atherinomorus vaigiensis, known only from eastern and western Australia, differs from other congeners in lacking a distinct tubercle on the posterior end of the dentary and having the posterior tip of the upper jaw not extending beyond a vertical through the anterior margin of the pupil, 12–15 anal fin soft rays, 24–28 lower gill rakers, 39–42 midlateral scales, and a narrow midlateral band (width about 2/3 to 5/6 that of midlateral scale at level of anal fin origin). Atherina cylindrica Valenciennes in Cuvier and Valenciennes, 1835 and Pranesus ogilbyi Whitely, 1930 are regarded as junior synonyms of Atherinomorus vaigiensis. Received: April 26, 2001 / Revised: July 11, 2001 / Accepted: July 16, 2001