Fine Structure of the Mesothelia and Extracellular Materials in the Coelomic Fluid of the Fin Boxes,Myocoels and Sclerocoels of a Lancelet,Branchiostoma floridae (Cephalochordata = Acrania)

Three ontogenetically related coeloms of a lancelet are described by transmission electron microscopy. The fin box coeloms are lined dorsally and laterally by smooth myomesothelial cells of uncertain function. In contrast, there are no myofilaments in the mesothelial cells of the ventral parts of the fin boxes. Similarly, myofilaments are absent from the mesothelia lining all parts of the sclerocoels and the lateral parts of the myocoels (the medial side of the myocoel is a myomesothelium comprising the striated muscles of the body wall). Lancelet coeloms differ from those of other deuterostomes in containing several kinds of formed extracellular materials. All three kinds of coeloms contain distinctive spherules with ramifying processes; dense strands are limited to the myocoels and sclerocoels; and a finely granular secretion is found only at the coelomic surface of the mesothelium lining the sclerocoels. These extracellular materials, which appear to originate from exocytosis of secretory granules from the mesothelial cells, may function biomechanically and for energy storage. The discussion includes a consideration of the so-called fin rays of lancelets and concludes that none of these structures is homologous with the fin rays of fish.     

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     

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.     

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.     

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.     

Ultrastructure of the glandular epidermis on the fins of male estuarine triplefins Forsterygion nigripenne

Male estuarine triplefins Forsterygion nigripenne develop enlarged fin tips during the breeding season. Using light microscopy and scanning and transmission electron microscopy the fins of males and females were compared. Tall columnar cells proliferated in the fin epidermis of males but were absent in females. The columnar cells were packed with proteinaceous granules that were bound by a double membrane. Three stages of development of columnar cells could be distinguished; the most mature expanded and ruptured to release its content. The function of the glandular epidermis is unknown but behavioural observations suggested that the secretion was applied to the egg mass and thus may protect it from infection.     

Ontogenetic variation in fin ray segmentation between latitudinal populations of the medaka, <Emphasis Type="Italic">Oryzias latipes</Emphasis>

Fin rays of ray-finned fishes are composed of multiple bony segments, and each fin ray elongates by adding a new segment to the tip. Therefore, fin ray length is determined by the number of segments and the length of each segment. A comparison of the anal fin rays of a northern and southern wild population of the medaka, Oryzias latipes, revealed that southern fish had more segments per fin ray, resulting in longer anal fins than the northern fish. When fish were reared in a laboratory common environment, segmentation of the fin rays started earlier with respect to body size in the southern fish. In the southern males, moreover, the rate of segment addition accelerated after a certain body size, indicating sexual maturity. These patterns of segment addition during ontogeny were consistent with the patterns of fin ray elongation. Although distal segments tended to be longer, except for the most proximal segment, in both populations, the southern fish had shorter segments than the northern fish at any position on fin rays. These results indicate that the interpopulation variation in fin length is largely due to genetically-based differences in the control of segment addition, and that the length of each segment does not contribute to it. We suspect that fin ray segmentation is regulated by thyroid and sex hormones that differ between populations. We also found that some segments fuse with each other at the base of each fin ray, the functions and mechanisms of which remain unclear.     

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.     

Reproduction and early development of a freshwater pipefish <Emphasis Type="Italic">Microphis leiaspis</Emphasis> in Okinawa-jima Island,Japan

We investigated the size at maturation, breeding season, and morphological development of larvae and juveniles of a freshwater pipefish Microphis leiaspis, which belongs to Gastrophori, collected from three rivers on the northern part of Okinawa-jima Island, Japan. The minimum size of brooding males was 105–123 mm in standard length (SL). The smallest mature female was estimated to be ca. 130 mm SL from the analysis of gonadosomatic index (GSI) and histological observations of gonads. The breeding season was estimated to be from June to December according to monthly changes in female GSI, histological observations of gonads, and monthly changes in the occurrence of brooding males. The number of eggs in the male brood pouch ranged from 75 to 241 (mean ± SD: 152 ± 52, n = 22). The male releases newly hatched larvae in freshwater areas. After newborns grow in the sea, they return to freshwater areas of the rivers and attain maturity. Microphis leiaspis was conformed to have an amphidromous life history. Notochord length of the released larvae was 6.1 mm, with a well-developed finfold. Larvae attained 11.1 mm SL, formation of the caudal and dorsal fin rays was complete, and the caudal fin became lozenge shaped at 30 days after the release, and juveniles reached 36.0 mm SL at 63 days after release. In the period between 30 and 63 days after the release, formation of all fins except the pectoral fins was completed, and caudal fin rays were extended and sector shaped with deep slits between each fin ray. The morphology of the released larvae of M. leiaspis is similar to that of Gastrophori species, and the morphology of juveniles similar to other species of Microphis.     

Morphology and histology of the anterior dorsal fin of Gaidropsarus mediterraneus (Pisces Teleostei), a specialized sensory organ

Summary The morphology and fine structure of the vibratile anterior dorsal fin of the rockling Gaidropsarus mediterraneus are described. 60–80 fin rays project as a fringe from a reduced fin web; their lateral movement maintains the fin in almost constant rapid undulation, at a frequency of 3–4 beats per second. The fin can be laid back and with-drawn into a groove. Erector and depressor muscles, which are histologically distinct, move each ray. The fin support is modified, incorporating elastic cartilage, and enclosed in a capsule of collagenous connective tissue. The epidermis at the frontal and caudal aspect of each ray contains numerous receptor cells, over 100,000 per mm², which have an apical microvillus and synaptic connections with nerve fibres. The recurrent facial nerve sends a major branch to the dorsal fins, which is joined by dorsal ramuli of spinal nerves. It is calculated that there are three to six million receptor cells on the vibratile fin and in the epidermis of the dorsal groove, in individuals of average size. Taste buds do not occur in the skin of the groove, contrary to a previous report, nor on the vibratile fin rays, although they are present on the prominent most anterior fin ray and elsewhere on the fins and barbels. The undulatory motion of the fin draws sea water towards and through the vibratile rays and backwards as a perceptible current. The fin constitutes a specific sensory organ, a water sampler, peculiar to this rockling and related species.Abbrevations used in figures a aperture - am axial muscles - bl base of lepidotrichion - cc collagenous capsule - dlc dorsal longitudinal canal - dr distal radial - drs dorsal ramulus of a spinal nerve - e epidermal cell(s) - ec elastic cartilage - en extracapsular branch of the recurrent facial nerve - fm fin membrane - fr fin ray - frn fin ray nerve - in intracapsular branches of the recurrent facial nerve - l lepidotrichia - n nerve plexus - ns neural spine - pr proximal radial - rc receptor cell(s) - rdm radial depressor muscle - rem radial erector muscle - s scales - t tendons Dedicated to Professor Konrad Lorenz on the occasion of his 80th birthday     

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 species of Gobius (Perciformes: Gobiidae) from the Mediterranean Sea and the redescription of Gobius bucchichi

A new species of the gobiid genus Gobius (Gobiidae, Perciformes), Gobius incognitus sp. nov. is described from the Mediterranean Sea, and its most morphologically similar species Gobius bucchichi is redescribed. The new species is distinguished from its congeners by: scales in lateral series 51–59; predorsal scales 25–35; opercle scaled in adults with 10–16 scales present; pectoral fin with ray count 18–20 and free tips on upper rays well developed and on the first ray longer than two thirds of the entire ray length; pelvic disc complete and with well‐developed anterior membrane without lateral lobes; anterior oculoscapular canal with pore α at rear of orbit; oculoscapular row x¹ not extending forwards to pore β; suborbital row d discontinuous with large gap below suborbital rows 3 and 4; eye diameter 1·08–1·32 in snout length; by pigment rows on cheek and pigmentation on pectoral‐fin base.     

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.     

Micro-anatomy of the pectoral fin in blennies (Blenniini, Blennioidea, Teleostei)

Blennioid fishes show a highly differentiated pectoral fin, which they use to cling to the substrate. The lower part of the pectoralis, comprising about four to six fin rays, forms a hook-field with specific anatomical features: (1) the rim of the fin web has a saw-like appearance, because it extends from the tip of a fin ray to the shaft ofthe upper of two neighbouring fin rays, (2) the outer half of the bony fin ray carries a lepidotrichal cord composed of fibrocytes, collagen, elastic fibres and acidic GAGS, (3) the epidermis overlying the lepidotrichal cord is differentiated in terms of cyto-architecture and forms a conspicuous cuticle. The upper part of the pectoral fin does not show any obvious specializations and is used for swimming and undulation. The vascularization of the fin originates from a stem vessel which gives rise to five branches, each supplying two or three neighbouring fin rays. Each fin ray is accompanied by a single arterial vessel at its upper edge. No vessels are found in the space between the bony fin ray halves. The morphology of the shoulder girdle and pectoral fin shows only little variation among the four species of Blenniini studied. Most remarkable is the fusion of the coracoid with the cleithrum, loss of one element of the suspensorium and the absence of branched fin rays. The possible relevance of the Blennioid pectoral fin as a model for the origin of morphological novelties in connection with functional specializations is discussed.     

Two new species of the genusAmblyeleotris (Pisces: Gobiidae) from the Ryukyu Islands,Japan

Two new shrimp-associated gobies,Amblyeleotris yanoi sp. nov. andA. masuii sp. nov. are described on the basis of specimens from Iriomote-jima Island and Okinawa-jima Islands, Okinawa Prefecture, Japan.A. yanoi is distinguished from other members of the genus by the combination of the following characters: 14 anal fin soft rays, 19 pectoral fin rays, 97–103 longitudinal scales, a candle flame-shaped marking on the caudal fin, a very low membrane connecting the pelvic fins and absence of a ventral frenum.A. masuii differs from all other congeners by having 92–97 longitudinal scales, the length of the interpelvic connecting membrane relative to the longest pelvic fin ray (0.43–0.66), black blotches on the sides of the chin, and blue spots on the opercle and preopercle.     

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 species of the genusamblyeleotris (pisces: Gobiidae) from Japan

A new shrimp-associated goby,Amblyeleotris melanocephala, is described on the basis of specimens from Okinoshima Island. Kochi Prefecture, and Okinawa Island, Okinawa Prefecture, Japan. The species is distinguished from other members of the genus by the following combination of characters: head dark brown, a few yellow spots on pectoral fin base and opercular margin, 13 second dorsal and 13 anal fin soft rays, 20 pectoral fin rays, longitudinal scales 92–101, proportional length of interpelvic connecting membrane relative to longest pelvic fin ray (CM-value) 0.46–0.55, presence of a ventral frenum, midline of nape naked, sides scaled above midpoint between preopercle and opercle.