Solitary chemoreceptor cells of Ciliata mustela (Gadidae, Teleostei) are tuned to mucoid stimuli

Summed potentials were recorded from the dorsal recurrent facialnerve innervating the solitary chemoreceptor cells on the anteriordorsal fin (ADF), from the ventral recurrent facial nerve innervatingboth taste buds and solitary chemoreceptor cells on the pectoral(PEC) and pelvic (PEL) fins, and from the anterior dorsal finmuscles in the rockling, Ciliata mustela. There is little overlapbetween the sumulus spectra of solitary chemoreceptor cellsand taste buds. The ADF solitary cells are particularly sensitiveto body mucus (skin water) of non-congeners like Gadus, Solea,Cottus, Mugil, Zoarces, Gaidropsarus, and Encheliopus, but insensitiveto amino acids and a variety of body fluids of fish, invertebrates,and extracts of potential stimuli like algae and sand. Pectoraland pelvic fins are particularly sensitive to amino acids, bodyfluids of fish and invertebrates, but less sensitive to skinmucus of fish, probably due to the abundance of taste buds.Active sampling by undulation of the anterior dorsal fin isessential for proper functioning; it induces disadaptation ofthe receptor elements. Solitary chemoreceptor cells provide,apparently, cues to discriminate between conspecifics and non-conspecifics.It is unlikely that they are involved in pheromone detection.     

Musculoskeletal morphology and regionalization within the dorsal and anal fins of bluegill sunfish (Lepomis macrochirus)

Ray‐finned fishes actively control the shape and orientation of their fins to either generate or resist hydrodynamic forces. Because of the emergent mechanical properties of their segmented, bilaminar fin rays (lepidotrichia), and actuation by multiple muscles, fish can control the rigidity and curvature of individual rays independently, thereby varying the resultant forces across the fin surfaces. Expecting that differences in fin‐ray morphology should reflect variation in their mechanical properties, we measured several musculoskeletal features of individual spines and rays of the dorsal and anal fins of bluegill sunfish, Lepomis macrochirus, and assessed their mobility and flexibility. We separated the fin‐rays into four groups based on the fin (dorsal or anal) or fin‐ray type (spine or ray) and measured the length of the spines/rays and the mass of the three median fin‐ray muscles: the inclinators, erectors and depressors. Within the two ray groups, we measured the portion of the rays that were segmented vs. unsegmented and branched vs. unbranched. For the majority of variables tested, we found that variations between fin‐rays within each group were significantly related to position within the fin and these patterns were conserved between the dorsal and anal rays. Based on positional variations in fin‐ray and muscle parameters, we suggest that anterior and posterior regions of each fin perform different functions when interacting with the surrounding fluid. Specifically, we suggest that the stiffer anterior rays of the soft dorsal and anal fins maintain stability and keep the flow across the fins steady. The posterior rays, which are more flexible with a greater range of motion, fine‐tune their stiffness and orientation, directing the resultant flow to generate lateral and some thrust forces, thus acting as an accessory caudal fin. J. Morphol., 2012. © 2011 Wiley Periodicals, Inc.     

The chemosensory anterior dorsal fin in rocklings (Gaidropsarus and Ciliata, Teleostei, Gadidae): activity, fine structure and innervation

Observations and experiments on the behaviour of shore rocklings have shown that the modified and vibratile anterior dorsal fin can be involved in the detection of food but is not essential to foraging by the fish. The epidermis of the vibratile fin rays contains numerous chemosensory cells, of similar cytology in the two species studied. These chemosensory cells are compared with the gustatory cells of the taste buds borne on other fin rays. Synaptic modifications in both cases consist of densities on the apposed membranes, with a dense layer under the membrane of the neurite more distinct than that in the cell. Vesicles are not a feature of these synapses, although some of the sensory cell bases are vesicular. Denervation experiments have shown that the chemosensory cells of the vibratile rays are supplied by a facial nerve component. After denervation a small proportion of the sensory cells were found to have an association with spinal nerve fibres. The present status of solitary chemosensory cells in fishes is discussed.     

The median‐fin skeleton of the Eastern Atlantic and Mediterranean clingfishes Lepadogaster lepadogaster (Bonnaterre) and Gouania wildenowi (Risso) (Teleostei: Gobiesocidae)

Previous research on the osteology of the Gobiesocidae focused mostly on the neurocranium and the thoracic sucking disc (formed by the paired‐fin girdles). Little attention has been paid to the skeleton of the median fins. The dorsal‐ and anal‐fin skeleton of Lepadogaster lepadogaster and other gobiesocids (excluding Alabes, which lacks these fins) are characterized by the absence of spines, branched fin‐rays, and middle radials. In gobiesocids, the distal radials never ossify and consist of elastic hyaline‐cell cartilage. Gouania wildenowi is unique among gobiesocids in having further reductions of the dorsal‐ and anal‐fin skeleton, including a notable decrease in the size of the proximal‐middle radials in an anterior–posterior direction. Unlike L. lepadogaster, which exhibits a one‐to‐one relationship between the dorsal‐ and anal‐fin rays and proximal‐middle radials, G. wildenowi has a higher number of proximal‐middle radials than distal radial cartilages and fin rays in the dorsal and anal fins. In G. wildenowi, the dorsal‐ and anal‐fin rays do not articulate with the distal tip of the proximal‐middle radials but are instead positioned between proximal‐middle radials, which is unusual for teleosts. Previously unrecognized dorsal and ventral pads of elastic hyaline‐cell cartilage are also present in the caudal skeleton of L. lepadogaster, G. wildenowi, and all other gobiesocids examined. J. Morphol., 2010. © 2009 Wiley‐Liss, Inc.     

Variation in flexural stiffness of the lepidotrichia within and among the soft fins of yellow perch under different preservation techniques

Although the ray‐finned fishes are named for their bony, segmented lepidotrichia (fin rays), we are only beginning to understand the morphological and functional diversity of this key vertebrate structure. Fin rays support the fin web, and their material properties help define the function of the entire fin. Many earlier studies of fin ray morphology and function have focused on isolated rays, or on rays from only one or two fins. At the same time, relatively little is known about how different preservation techniques affect the material properties of many vertebrate structures, including fin rays. Here, we use three‐point bending tests to examine intra‐ and inter‐fin variation in the flexural stiffness of fin rays from yellow perch, Perca flavescens. We sampled fin rays from individuals that were assigned to one of three preservation treatments: fresh, frozen, and preserved with formalin. The flexural stiffness of the fin rays varied within and among fins. Pelvic‐fin rays were the stiffest, and pectoral fin rays the least stiff. The fin rays of the dorsal, anal, and caudal fins all had similar stiffness values, which were intermediate relative to those from the paired fins. The flexural stiffness of the fin rays was higher in rays that were at the leading edge of the fin. This variation in flexural stiffness was associated with variation in joint density and the relative length of the unsegmented proximal base of the fin rays. There was no significant difference in flexural stiffness between fresh and frozen specimens. In specimens preserved with formalin, there is a small but significant effect on stiffness in smaller fin rays.     

Rhodeus pseudosericeus sp. nov., a new bitterling from South Korea (Cyprinidae, Acheilognathinae)

A new bitterling, Rhodeus pseudosericeus sp. nov., is described on the basis of 31 specimens from five localities included in the Namhan River system, South Korea. The new species is distinguished from other Rhodeus species by the following combination of characters: branched dorsal fin rays 9–10 (mode 9); branched anal fin rays 9–11 (mode 10); longest simple ray of dorsal fin strong and stiff, distally segmented; pelvic fin rays i, 6–7; iris of males blackish; dorsal and anal fins of males grayish in breeding season; karyotype with 2n = 48 (8m + 20sm + 20st). Rhodeus pseudosericeus sp. nov. is similar to Rhodeus sericeus sericeus in the number of pelvic fin and branched dorsal fin rays and the melanophores present on the dorsal fin membrane, but differs from the latter in having a greater body depth, more branched anal fin rays, fewer vertebrae, a lower number of scales in the lateral series, and differing male nuptial coloration. Received: June 30, 2000 / Revised: February 21, 2001 / Accepted: March 6, 2001     

A larva of Coryphaenoides pectoralis (Gadiformes: Macrouridae) collected by deep-sea submersible from off Hokkaido, Japan

A late-stage larva of Coryphaenoides pectoralis was first observed in situ and subsequently collected by the deep-sea submersible “Shinkai 2000” from mesopelagic waters at a depth of 530 m off Hokkaido, Japan. The larva (14.5 mm in head length, 149+ mm in total length) has fan-like pectoral fins, elongate first dorsal fin, pelvic fin and tail, 10 first dorsal rays (including 2 pseudospines), and 7 pelvic fin rays, 6 branchiostegal rays, no light organ, anus just anterior to anal fin origin, 2 retia and gas glands, 14 abdominal vertebrae, and previously reported larval pigmentation. Counts of second dorsal and anal fin rays, and caudal vertebrae, are reported for the first time.     

Peripheral nervous system of the ocean sunfish Mola mola (Tetraodontiformes: Molidae)

Dissection of peripheral nerves in the ocean sunfish Mola mola showed the lateral line system to comprise 6 cephalic and 1 trunk lateral lines, all neuromasts being superficial. The trunk line was restricted to the anterior half of the body, the number of neuromasts (27) being fewer than those previously recorded in other tetraodontiforms. The lateral ramus of the posterior lateral line nerve did not form a “serial collector nerve” along the body. The number of foramina in the neurocranium, serving as passages for the cranial nerves, was fewer than in primitive tetraodontiforms, the reduction being related to modifications in the posterior cranium. Some muscle homologies were reinterpreted based on nerve innervation patterns. The cutaneous branch innervation pattern in the claval fin rays was clearly identical with that in the dorsal and anal fin rays, but differed significantly from that in the caudal fin rays, providing strong support for the hypothesis that the clavus comprises highly modified components of the dorsal and anal fins.     

A comparison of pectoral fin ray morphology and its impact on fin ray flexural stiffness in labriform swimmers

The organization of tissues in appendages often affects their mechanical properties and function. In the fish family Labridae, swimming behavior is associated with pectoral fin flexural stiffness and morphology, where fins range on a continuum from stiff to relatively flexible fins. Across this diversity, pectoral fin flexural stiffness decreases exponentially along the length of any given fin ray, and ray stiffness decreases along the chord of the fin from the leading to trailing edge. In this study, we examine the morphological properties of fin rays, including the effective modulus in bending (E), second moment of area (I), segmentation, and branching patterns, and their impact on fin ray stiffness. We quantify intrinsic pectoral fin ray stiffness in similarly sized fins of two closely related species that employ fins of divergent mechanics, the flapping Gomphosus varius and the rowing Halichoeres bivittatus. While segmentation patterns and E were similar between species, measurements of I and the number of fin ray branch nodes were greater in G. varius than in H. bivittatus. A multiple regression model found that of these variables, I was always significantly correlated with fin ray flexural stiffness and that variation in I always explained the majority of the variation in flexural stiffness. Thus, while most of the morphological variables quantified in this study correlate with fin ray flexural stiffness, second moment of area is the greatest factor contributing to variation in flexural stiffness. Further, interspecific variation in fin ray branching pattern could be used as a means of tuning the effective stiffness of the fin webbing to differences in swimming behavior and hydrodynamics. The comparison of these results to other systems begins to unveil fundamental morphological features of biological beams and yields insight into the role of mechanical properties in fin deformation for aquatic locomotion.     

A new pearleye (Teleostei,Aulopiformes) species from the Oligocene of Romania

A new pearleye species of the alepisauroid family Scopelarchidae, Scopelarchoides neamticus sp. nov., is described herein based on two specimens from the Oligocene Lower Dysodilic Shales Formation, cropping out in the Pietricica Mountain, Romanian Eastern Carpathians. The new species described herein exhibits a unique combination of features (including head length about 25% of SL; coracoid remarkably expanded; both preorbital and postorbital lengths larger than orbit diameter; 50 or 51 vertebrae; dorsal fin with nine or ten rays; anal-fin with 28 rays; length of anal fin base about 30% of SL; preanal distance almost 60% of SL; pelvic fin insertion located just under the second dorsal fin ray; pectoral fins only slightly longer than pelvic fins; caudal fin with 19 principal rays plus 14 upper and 13 lower procurrent rays) that justifies its recognition as a new species of the genus Scopelarchoides. Both morphological and meristic features suggest a certain degree of similarity between S. neamticus sp. nov. and the extant species Scopelarchoides signifer. The fossils of the new Oligocene species described herein represent the oldest known skeletal record of Scopelarchidae.     

The dorsal fin engine of the seahorse (Hippocampus sp.)

The muscles, fin ray joints, and supporting structures underlying the dorsal fin are described for two seahorse species: Hippocampus zosterae and Hippocampus erectus. A fan-shaped array of cartilaginous bones, the pterigiophores, form the internal supporting structure of the dorsal fin. Each pterigiophore is composed of a proximal radial that extends from a vertebra to the dorsal side of the animal, where it fuses to a middle radial. The middle radials fuse with each other to form a dorsal ridge upon which sit the spheroidal distal radials. Each distal radial articulates with a fin ray on its dorsal side and is attached to the dorsal ridge on its ventral side by a material that has been histologically identified as elastic cartilage. Together these connections form a two-axis joint that permits elevation, depression, and inclination of the ray. Each fin ray is actuated by two bilateral pairs of muscles, an anterior pair of inclinators, and a posterior pair of depressors. The anteriormost fin ray is actuated by three bilateral pair of muscles, the inclinators, the depressors, and a pair of elevator muscles that are positioned anterior to the inclinators. Preliminary examinations of the ray joints of the pectoral and anal fins of adult H. zostera and the pectoral fins of newborn H. erectus revealed structures similar to that seen in the dorsal fins. To further explore the structure and function of the dorsal fin gross dissections and simple functional tests were performed on H. erectus and H. barbouri and behavioral observations were made of all three species plus Hippocampus kuda.     

Atrosalarias hosokawai, a new species of blenny (perciformes: Blenniidae) from the western pacific

A new species of blenny,Atrosalarias hosokawai is described on the basis of 15 specimens from the western Pacific. It is distinguished from the only known congeneric species,A. fuscus (=A. fuscus fuscus+A. fuscus holomelas), by the following: supraorbital cirrus broad and flat (vs. slender and thread-like inA. fuscus); dorsal fin broadly contacting caudal fin (vs. narrow contact); anal fin narrowly contacting caudal fin (vs. usually free or (rarely) very narrow contact); posteriormost dorsal and anal fin rays long (vs. short); first or posteriormost soft dorsal fin ray shortest (vs. posteriormost ray shortest); first soft anal fin ray shortest (vs. posteriormost ray shortest); caudal fin rays branched in specimens over 36.0 mm SL (vs. unbranched); a large dark spot on base of pectoral fin absent (vs. present or absent); a red margin on anterior dorsal fin absent (vs. present). Futhermore,A. hosokawai differs fromA. f. fuscus in having a lower number of dorsal fin spines (ten vs. eleven) and geographical distribution (western Pacific Ocean vs. Indian Ocean and Red Sea). AlthoughA. hosokawai occurs sympatrically withA. f. holomelas, it can be further distinguished from the latter in lacking a large dark spot on base of pectoral fin.     

Skeletal ontogeny of the vertebral column and of the fins in shi drum Umbrina cirrosa (Teleostei: Perciformes: Sciaenidae), a new candidate species for aquaculture

The osteological development of the vertebral column and fins in shi drum Umbrina cirrosa was studied in order to improve knowledge for its introduction in Mediterranean aquaculture. The osteological development was studied in 171 individuals, of total length (L_T) from 2·7 to 30·2 mm that were reared under the mesocosm technique. Vertebral ontogeny starts at 3·4 and 4·0 mm L_T, with the formation of the first cartilaginous neural and haemal arches, and spines, respectively, and is completed with the full attainment of epicentrals (12·5 mm L_T). The formation of vertebral centra occurs between 4·1 and 7·4 mm L_T. Pectoral supports are the first fin elements to develop (3·0 mm L_T), followed by those of the caudal fin (3·8 mm L_T), pelvic fin (3·9 mm L_T) and finally by those of the dorsal and anal fins (4·5 mm L_T). The caudal fin is the first to develop fin rays and attain the full count of principal fin rays (4·5–6·8 mm L_T), but the last to be fully completed with the formation of procurrent fin rays (6·9–17·5 mm L_T). The next fins starting to present rays are the dorsal (5·3 mm L_T) and the pectoral fins (5·6 mm L_T), while the anal and pelvic fins are the last (5·7 mm L_T). Following the caudal principal fin rays (6·8 mm L_T), the dorsal, anal (6·9 mm L_T), pelvic (7·4 mm L_T) and pectoral fins (9·8 mm L_T) are the next with fully completed ray counts. Aggregation of qualitative changes, such as the appearance of cartilages, the beginning and the complement of the ossification process and the full complement of elements in U. cirrosa were measured as cumulative frequency counts. These measurements reveal three ontogenetic intervals: one very developmentally active period during early life stages (from 3 to 5·9 mm L_T), a second slower developmental period (from 6·0 to 8·9 mm L_T) and finally a period of ontogeny more focused on structure refinement up to metamorphosis and settlement (>9·0 mm L_T).     

A new loach, Cobitis shikokuensis (Teleostei: Cobitidae), from Shikoku Island, Japan

A new species of spinous loach, Cobitis shikokuensis, is described based on 297 specimens from Shikoku Island, Japan. The new species was formerly known as the Shikoku group of Cobitis takatsuensis. It can be distinguished from other species of Cobitis and closely related genera by a combination of the following characters: dorsal fin with 6 branched soft rays; anal fin with 5 branched soft rays; one brownish streak across eye from the tip of nose, no streak on cheek; a black spot smaller than eye diameter near the dorsal corner of the caudal fin base; 3–5 small brownish speckles on ventral side of caudal peduncle; high caudal peduncle with well-developed fleshy keels on dorsal and ventral side; a lamina circularis at base of dorsal part of pectoral fin absent; first branched soft ray of pectoral fin broad in males; pectoral soft rays widely branched from the approximate midpoint; last anal fin ray with 2 elements; interorbital width 11.2–17.1% of head length.     

广西高原鳅属鱼类一穴居新种记述

2003年1月,在广西壮族自治区天峨县红水河水系地下河采集到一批盲鱼标本。经鉴定,为高原鳅属Triplophysa一未经发表的新种。新种天峨高原鳅Triplophysa tianeensis sp．nov．与个旧盲高原鳅T．gejiuensis、石林盲高原鳅T．shilinensis、阿庐高原鳅T．aluensis和南丹高原鳅T．nandanensis相似;本新种腹鳍末端不达肛门,尾鳍分枝鳍条16,可进一步与个旧盲高原鳅和石林盲高原鳅(腹鳍末端达到肛门,尾鳍分枝鳍条14-15)相区别;本新种背鳍起点位于体之中点、腹鳍起点之后,肛门紧靠臀鳍起点,可进一步与阿庐高原鳅(背鳍起点靠近吻端、位于腹鳍起点之前,肛门距臀鳍起点仍有一段距离)相区别。本新种与同分布于红水河水系的南丹高原鳅Triplophysa nandanensis Lan et al.较为相似;但二者区别明显：新种背鳍分枝鳍条7、胸鳍分枝鳍条9、腹鳍分枝鳍条6、背鳍外缘平截、背鳍起点位于腹鳍起点之后,后者背鳍分枝鳍条8、胸鳍分枝鳍条10～11、腹鳍分枝鳍条7、背鳍外缘凹入、背鳍起点位于腹鳍起点之前;此外,新种的穴居特征更为显著：眼极度退化、头长为眼径16．8—32．8(25．0)倍、部分个体无色素斑且各鳍无斑点,而南丹高原鳅眼小、头长为眼径4．7～9．0(7．5)倍、体和头背侧密布云状斑且各鳍均具点状斑。     

Stiphodon niraikanaiensis,a new species of sicydiine goby from Okinawa Island (Gobiidae: Sicydiinae)

A new goby species, Stiphodon niraikanaiensis, is described on the basis of three specimens (two females and one male) collected from a freshwater stream in Okinawa Island, Japan. This species can be distinguished from its congeners by nine soft rays in the second dorsal fin, 16 rays in the pectoral fin, a pointed first dorsal fin in male, the premaxilla with 46–50 tricuspid teeth in 27–36 mm SL; no white patch behind the pectoral-fin base in male, the nape and posterior half of the occipital region covered by cycloid scales, broad black band along the distal margin of the second dorsal fin in male, 11 or 12 dusky transverse bars laterally on the trunk and tail of female intersecting with the mid-lateral longitudinal band, several conspicuous black spots on each spine and soft ray on the first and second dorsal fins of female, the anal fin of female lacking remarkable marking, and the pectoral-fin rays with 2–5 and 1–4 black spots, respectively, for male and female. The new species is known only from the type locality.     

Schindleria elongata,a new species of paedomorphic gobioid from the Red Sea (Teleostei: Schindleriidae)

A new species of paedomorphic gobioid, Schindleria elongata, from the Red Sea, is described on the basis of five specimens. The new species is characterized by its lack of body pigmentation; the body depth at pectoral‐fin origin 4–5% of standard length (L_S) and at anal‐fin origin 5–7% L_S; the predorsal length 66–70% L_S; pre‐anal length 66–71% L_S; dorsal‐fin rays 13 or 14; anal‐fin rays 10 or 11; first dorsal‐fin ray at myomere 20 or 21; first anal‐fin ray below second to fourth dorsal‐fin rays; myomeres 19 or 20 + 13 or 14 = 33 or 34 total; premaxillae and dentaries with small teeth; gas bladder located posteriorly at 56–60% L_S; males with a rod‐like, flexible urogenital papilla lacking lobes, projections or accessory papillae, with distal half tapering to a broad, angular point and usually posteriorly directed. A key to the species of Schindleriidae is presented.     

Descriptive morphology of pelagic juvenile of <Emphasis Type="Italic">Lepidion inosimae</Emphasis> (Gadiformes: Moridae) collected from off northeastern Japan

A pelagic juvenile (74.0 mm in standard length) of Lepidion inosimae was collected by midwater trawl (0–20 m depth) from the transition waters between the Kuroshio and Oyashio fronts off northeastern Japan. The specimen is characterized by an elongate body, a chin barbel, a minute first ray and non-elongated second ray of first dorsal fin, combination of 55 second dorsal fin rays and 52 anal fin rays, and no ventral luminous organ. This is the first report of early life stages in the genus Lepidion.     

A new marine goby of genus Callogobius (Teleostei: Gobiidae) from Taiwan

A new marine goby Callogobius sheni collected from coral reefs off southern Taiwan is described. The new species can be distinguished from congeneric species by the following combination of features: dorsal fin rays VI-I, 9; anal fin rays I, 7; pectoral fin rays 18; longitudinal scale rows 27–28; predorsal scale rows 9–10; no posterior oculoscapular and preopercular canals; body pale white with five blackish brown cross bands; caudal and pectoral fins each with a large blackish brown blotch.