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.     

The evolution of underwater flight: The redistribution of pectoral fin rays,in manta rays and their relatives (Myliobatidae)

Batoids are a diverse clade of flat cartilaginous fishes that occur primarily in benthic marine habitats. The skates and rays typically use their flexible pectoral fins for feeding and propulsion via undulatory swimming. However, two groups of rays have adopted a pelagic or bentho‐pelagic lifestyle and utilize oscillatory swimming—the Myliobatidae and Gymnuridae. The myliobatids have evolved cephalic lobes, anteriorly extended appendages that are optimized for feeding, while their pectoral fins exhibit several modifications that likely arose in association with functional optimization of pelagic cruising via oscillatory flight. Here, we examine variation in fin ray distribution and ontogenetic timing of fin ray development in batoid pectoral fins in an evolutionary context using the following methods: radiography, computed tomography, dissections, and cleared and stained specimens. We propose an index for characterizing variation in the distribution of pectoral fin rays. While undulatory swimmers exhibit symmetry or slight anterior bias, we found a posterior shift in the distribution of fin rays that arose in two distinct lineages in association with oscillatory swimming. Undulatory and oscillatory swimmers occupy nonoverlapping morphospace with respect to fin ray distribution illustrating significant remodeling of pectoral fins in oscillatory swimmers. Further, we describe a derived skeletal feature in anterior pectoral fins of the Myliobatidae that is likely associated with optimization of oscillatory swimming. By examining the distribution of fin rays with clearly defined articulation points, we were able to infer evolutionary trends and body plan remodeling associated with invasion of the pelagic environment. Finally, we found that the number and distribution of fin rays is set early in development in the little skate, round stingray, and cownose ray, suggesting that fin ray counts from specimens after birth or hatching are representative of adults and therefore comparable among species.     

A new gobiid fish of the genusClariger from Mutsu Bay,northern Japan

A new species of the genusClariger was described on the basis of thirty-two specimens collected from the subtidal zone of Mutsu Bay, Aomori Pref. This species is distinguishable from other congeners in the following: body naked; a series of large white patches on the back, one on the nape passing through the pectoral fin base and axil part; fin rays of both the second dorsal and anal fins, I, 12–14; vertebrae, 34–35; a single free filamentous ray on the upper lobe of pectoral fin. A new key to all the known species of the genusClariger is prepared.     

Posterior<Emphasis Type="Italic"> hoxa</Emphasis> genes expression during zebrafish bony fin ray development and regeneration suggests their involvement in scleroblast differentiation

Expression of two zebrafish developmental posterior hoxa genes, hoxa11b and hoxa13b, was studied by in situ hybridization during pectoral and caudal fin development and regeneration. Expression was restricted to cells of the bony rays region. During fin development, molecular cytological analysis revealed that a subpopulation of mesenchymal cells expressed these two hoxa genes during their early differentiation in the subapical region of the developing ray. These cells were identified as differentiating dermal bone making cells (scleroblasts). During fin regeneration, hoxa11b and hoxa13b genes are both induced in undifferentiated cells of the distalmost blastema region (DMB) and the proliferating zone (PZ) and later in differentiating bone-forming cells. In addition, the transient regionalization of the hoxa13b expression pattern in differentiated bone-forming cells along the proximodistal axis of the regenerating ray suggests that hoxa13b could participate in ray patterning. This study is the first to establish a correlation between hoxa gene expression and dermal bone cell differentiation.     

Batoid wing skeletal structure: novel morphologies, mechanical implications, and phylogenetic patterns

The skeleton of the "wings" of skates and rays consists of a series of radially oriented cartilaginous fin rays emanating from a modified pectoral girdle. Each fin ray consists of small, laterally oriented skeletal elements, radials, traditionally represented as simple cylindrical building blocks. High-resolution radiography reveals the pattern of calcification in batoid wing elements, and their organization within the fin ray, to be considerably more complex and phylogenetically variable than previously thought. Calcification patterns of radials varied between families, as well as within individual pectoral fins. Oscillatory swimmers show structural interconnections between fin rays in central areas of the wing. Morphological variation was strongly predictive of locomotor strategy, which we attribute to oscillatory swimmers needing different areas of the wing stiffened than do undulatory swimmers. Contributions of various forms of calcification to radial stiffness were calculated theoretically. Results indicate that radials completely covered by mineralized tissue ("crustal calcification") were stiffer than those that were calcified in chain-like patterns ("catenated calcification"). Mapping this functionally important variation onto a phylogeny reveals a more complicated pattern than the literature suggests for the evolution of locomotor mode. Therefore, further investigation into the phylogenetic distribution of swimming mode is warranted.     

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.     

A new cave‐dwelling loach,Triplophysa xichouensis sp. nov. (Teleostei Nemacheilidae) from Yunnan,China

A new cave‐dwelling loach of the genus Triplophysa, T. xichouensis, is described from an outlet of a subterranean river in Xisa Town, Xichou County, Yunnan Province, China. It can be distinguished from its congeners by the following characters: dorsal‐fin rays iii, 8; anal‐fin rays ii, 6; pectoral‐fin rays i, 9 or 10; pelvic‐fin rays i, 5 or 6; branched caudal‐fin rays 16(8+8); eyes highly degenerated to a very tiny black dot; dorsal‐fin origin closer to snout tip than to caudal‐fin base and anterior to vertical line of pelvic‐fin origin; pectoral fin length about two‐thirds the distance between pectoral‐fin origin to pelvic‐fin origin; caudal peduncle slender, its length about three times its depth; caudal fin emarginate; body smooth and scaleless; lateral line complete and straight; anterior chamber of air bladder wrapped in dumbbell‐shaped bony capsule and the posterior one well developed, long, oval; intestine short, bending in zigzag shape behind stomach. A key for the cave‐dwelling species of Triplophysa is provided. urn:lsid:zoobank.org:pub:9162FFB1‐7911‐47C3‐AE50‐6A00E9590327     

Functional morphology of the fin rays of teleost fishes

Ray‐finned fishes are notable for having flexible fins that allow for the control of fluid forces. A number of studies have addressed the muscular control, kinematics, and hydrodynamics of flexible fins, but little work has investigated just how flexible ray‐finned fish fin rays are, and how flexibility affects their response to environmental perturbations. Analysis of pectoral fin rays of bluegill sunfish showed that the more proximal portion of the fin ray is unsegmented while the distal 60% of the fin ray is segmented. We examined the range of motion and curvatures of the pectoral fin rays of bluegill sunfish during steady swimming, turning maneuvers, and hovering behaviors and during a vortex perturbation impacting the fin during the fin beat. Under normal swimming conditions, curvatures did not exceed 0.029 mm^?1 in the proximal, unsegmented portion of the fin ray and 0.065 mm^?1 in the distal, segmented portion of the fin ray. When perturbed by a vortex jet traveling at approximately 1 ms^?1 (67 ± 2.3 mN s.e. of force at impact), the fin ray underwent a maximum curvature of 9.38 mm^?1. Buckling of the fin ray was constrained to the area of impact and did not disrupt the motion of the pectoral fin during swimming. Flexural stiffness of the fin ray was calculated to be 565 × 10^?6 Nm². In computational fluid dynamic simulations of the fin‐vortex interaction, very flexible fin rays showed a combination of attraction and repulsion to impacting vortex dipoles. Due to their small bending rigidity (or flexural stiffness), impacting vortices transferred little force to the fin ray. Conversely, stiffer fin rays experienced rapid small‐amplitude oscillations from vortex impacts, with large impact forces all along the length of the fin ray. Segmentation is a key design feature of ray‐finned fish fin rays, and may serve as a means of making a flexible fin ray out of a rigid material (bone). This flexibility may offer intrinsic damping of environmental fluid perturbations encountered by swimming fish. J. Morphol. 274:1044–1059, 2013. © 2013 Wiley Periodicals, Inc.     

The pectoral anatomy of selected Ostariophysi. I. The Characiniformes.

The muscles and bones of the pectoral fin of Serrasalmus nattereri, the piranha, resemble those of generalized, lower teleosts with specializations related to a body shape adapted for high-speed carnivory; the pectoral fins being highly mobile with strong ligaments to the rays. The presence of two occipital nerves appears primitive, while the emergence of the subclavian artery within the branchial cavity, as in Gasteropelecus sternicla, appears specialized. The muscles and bones of the latter fish, a fresh-water flying fish, are specialized for self-propelled, aerial flight in the fusion of the right and left girdles greatly expanded for insertions of complex appendicular (flight) muscles, and in the consolidation of the rays and radials into one functional unit moving vertically in flight through contraction of vertical, massive ventral flight muscles. The bony pectoral anatomy of Electrophorus electricus, the electric eel, is specialized in having a mobile joint between the primary girdle and the cleithrum, the former being suspended vertically from the cleithrum by ligaments. The proximal radials and rays are very numerous and vertically aligned. The cleithrum is shaped to accommodate the extensive sternohyoid and pharyngocleithral muscles. The sheet-like appendicular muscles extend beyond the special joint and control its movement. The deeper muscles do not cross this joint. The arterial system is specialized in lacking a deep brachial artery.     

A new species of <Emphasis Type="Italic">Rhinogobius</Emphasis> (Teleostei: Gobiidae) from the Feiyunjiang Basin in Zhejiang Province,China

A new freshwater goby, Rhinogobius wuyanlingensis, was collected from Wuyanling National Natural Conservation Area, Taishun, Zhejiang Province, China. The species can be distinguished from all congeneric species by the following unique combination of features: second dorsal fin rays modally I, 8; anal fin rays I, 8; pectoral fin rays modally 18; longitudinal scale series 30–32; predorsal scales 7–9; vertebral count 10 + 17 = 27; body always with six longitudinal pinkish orange to grayish brown lines from dorsal to ventral region in male; cheek spotless; branchiostegal membrane deep grayish with 6–7 long, transverse deep red stripes in male; chin always deep grayish; first dorsal fin with two long black blotches on membranes anterior to third spinous ray in male; second dorsal fin whitish with three to four horizontal rows of light spots in male; caudal fin base with a large blackish-brown spot; and pectoral fin with a horizontal, median blackish brown line. An artificial key to all five nominal species with a high vertebral count (27–29) from Zhejiang Province from China is also provided.     

Comparing aging precision of calcified structures in shovelnose sturgeon

Age estimates for population analysis must be precise. We assessed the usefulness of pectoral fin rays, sphenoids, opercula, and dorsal scutes of shovelnose sturgeonScaphirhynchus platorynchus (n = 30) as aging structures based on ease of collection, distinctness of annuli, and measures of precision both between and within readers. We also determined how age estimates from paired fin rays of individuals were related (n = 106). Pectoral fin rays generated the highest within‐reader precision (100% within 2 years) followed by sphenoids (58%), opercula (56%), and dorsal scutes (49%). Ages estimated by the pectoral fin ray also had higher between‐reader agreement (80% within 1 year) than did those from the operculum (60%), sphenoid (59%), or dorsal scute (56%). Likewise, age estimates from pectoral fin rays had the lowest mean coefficient of variation (8.2%) followed by sphenoids (9.9%), opercula (11.3%), and dorsal scutes (11.5%). Only the operculum produced biased estimates between readers. Ages from paired fin rays agreed poorly (36% exact, 30% within 1 year) although no aging bias occurred. The pectoral fin ray is typically used to age shovelnose sturgeon. Because uncertainty about accuracy and precision of age estimates from this structure remains, shovelnose sturgeon management objectives that result from age data should remain conservative.     

A new cave-dwelling loach, Triplophysa macrocephala (Teleostei: Cypriniformes: Balitoridae), from Guangxi, China

A new cave-dwelling species, Triplophysa macrocephala sp. nov. is described based on specimens collected from a karst cave in Renguang village, Lihu Town, Nandan County, Guangxi Zhuang Autonomous Region, China. The new species can be distinguished from its congeners by possessing the following combination of characters: pectoral fin not reaching beyond pelvic-fin origin; caudal fin forked; body smooth or scaleless; dorsal-fin origin anterior to pelvic-fin origin, edge of dorsal fin truncate; dorsal fin with eight branched rays; anal fin with five branched rays; eye small and vestigial; lower jaw arched with a median notch; air-bladder wrapped in bony capsule, lateral enlarged, posterior chamber of air-bladder degenerated.     

<Emphasis Type="Italic">Cobitis elazigensis</Emphasis>, a New Species of Cobitidid Fish from Anatolia,Turkey

A new cobitidid, Cobitis elazigensis, is described from Anatolian Turkey in the province of Elazi?. The new species differs from all other members of the genus by having the following combination of characters: two Canestrini’s scales on the pectoral fin, a suborbital spine with a dorso-lateral branch (rarely simple and unbranched), large size, over 180 mm total length, total vertebrae 47–49, lateral spots reduced or absent, a spot at the upper caudal fin base, scales longer than wide with a small focus, dorsal fin rays III, 5–6, usually 6, ventral fin rays III, 6–7, usually 6, and pectoral fin rays I, 7–9.     

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.     

Evidence of a counter-current heat exchanger in the ray, Mobula tarapacana (Chondrichthyes: Elasmobranchii: Batoidea: Myliobatiformes)

A vascular network, or rete, has been found in the pectoral fin of the mobulid ray, Mobula tarapacana. This rete appears to be a counter-current heat exchanger which, in conjunction with a high level of red muscle, indicates that this ray is warm-bodied. Preliminary results on other closely related rays indicate that retia may be more common amongst the rays than previously thought.     

Channa panaw, a new channid fish from the Irrawaddy and Sittang River basins, Myanmar

Channa panaw sp. nov. (Channidae) is described from 32 specimens collected from the Irrawaddy and Sittang River basins, Myanmar. It is distinguishable from all known congeners by the combination of the following characters: 32–35 dorsal fin rays, 23–24 anal fin rays, 17–20 pectoral fin rays, 39–41 lateral line scales, 39–41 total vertebrae, one large scale on each side of the lower jaw (rarely 2 on one side), pelvic fin length always more than 50% of pectoral fin length, and 7–12 irregular black blotches on the upper half of the body.     

<Emphasis Type="Italic">Careproctus surugaensis</Emphasis> sp. nov. (Liparidae), a new snailfish from Suruga Trough,Japan

A new species of liparid fish Careproctus surugaensis is described from a single specimen collected between 1,450 and 1,570 m depth on the northern part of Suruga Trough, Suruga Bay, Japan. It can be distinguished from all currently recognized congeners by the following combination of characters: 50 total vertebrae, 47 dorsal-fin rays, 39 anal-fin rays, 32 pectoral-fin rays, 10 principal caudal-fin rays, pectoral proximal radials 4 (first to third with notches); trilobate teeth on both jaws, gill slit 7.1 % SL, extending in front of 7th pectoral fin ray base; maximum body depth 19.1 % SL, disk length 7.9 % SL, anus midway between posterior margin of pelvic disk and anal-fin origin; body and fins light orange except blackish peritoneum.     

中国贵州省穴居盲鳅一新种(鲤形目,爬鳅科)

记述了采集于贵州省荔波县佳荣镇水井湾溶洞(25°28’N,108°06’E)适应洞穴环境的鳅类1新种:佳荣盲高原鳅Triplophysa jiarongensis sp.nov.。新种与之前记录的7种分布于西江水系的高原鳅(阿庐高原鳅、个旧盲高原鳅、长须盲高原鳅、巨头高原鳅、邱北盲高原鳅、石林盲高原鳅和天峨高原鳅)同属典型洞穴鱼类,都具有一系列与洞穴环境有关的适应性特征。新种与本属其它种类的区别主要为:胸鳍长,后伸达腹鳍起点;尾鳍微凹形;体表色素退化,光滑裸露无鳞;背鳍截形,起点位于腹鳍起点略后方;腹鳍后伸盖过泄殖孔;臀鳍截形;尾柄上下缘存在脂状鳍褶;背鳍分支鳍条8;臀鳍分支鳍条6;胸鳍分支鳍条11;脊椎骨总数4+34;眼完全退化,外观无痕迹;鳔前室被骨质鳔囊包裹,后室发达膨大呈游离膜质鳔。此外还介绍了其栖息地概况和部分生态学信息。     

Review of the genusBembras Cuvier, 1829 (Scorpaeniformes: Bembridae) with description of three new species collected from Australia and Indonesia

The bembrid genusBembras Cuvier is reviewed. Five species,B. japonica Cuvier,B. adenensis Imamura & Knapp and three undescribed species, were assigned to the genus. Type species of the genus,Bembras japonica is redescribed on the basis of 36 specimens including the holotype, and three new species,B. macrolepis, B. longipinnis andB. megacephala, previously misidentified asB. japonicus, are also described on the basis of specimens collected from Australia and Indonesia.Bembras macrolepis differs from its congeners by having large body scales, a long pectoral fin with 17–19 rays and a dark blotch on slightly upper portion to middle of margin, 14–15 anal-fin rays, small head and orbit, and caudal fin with a broad vertical dark band near posterior margin.Bembras longipinnis is distinguished from other members of the genus by having a slightly long pectoral fin with 17–19 rays and lacking a small black blotch near tip of upper rays, caudal fin with a large dark spot most intense in lower lobe, 1–2 gill rakers on upper gill arch, 13–14 anal-fin rays, slightly elong ated head and small orbit.Bembras megacephala is characterized by the following combination of characters: caudal fin with several irregular narrow vertical dark bands, small orbit, pectoral fin with 19–20 rays and lacking a small black blotch near tip of upper rays, head elongate, 2–4 gill rakers on upper gill arch, 15 anal-fin rays and small body scales. A key separating the five species ofBembras is given.