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.     

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.     

Structure of supporting elements in the dorsal fin of percid fishes

The dorsal fin is one of the most varied swimming structures in Acanthomorpha, the spiny‐finned fishes. This fin can be present as a single contiguous structure supported by bony spines and soft lepidotrichia, or it may be divided into an anterior, spiny dorsal fin and a posterior, soft dorsal fin. The freshwater fish family Percidae exhibits especially great variation in dorsal fin spacing, including fishes with separated fins of varying gap length and fishes with contiguous fins. We hypothesized that fishes with separated dorsal fins, especially those with large gaps between fins, would have stiffened fin elements at the leading edge of the soft dorsal fin to resist hydrodynamic loading during locomotion. For 10 percid species, we measured the spacing between dorsal fins and calculated the second moment of area of selected spines and lepidotrichia from museum specimens. There was no significant relationship between the spacing between dorsal fins and the second moment of area of the leading edge of the soft dorsal fin.     

Lessons from the first dorsal fin in atheriniforms—A new mode of dorsal fin development and its phylogenetic implications

The median fins in extant actinopterygians are the product of millions of years of evolution. During this time, different developmental patterns for the dorsal and anal fins emerged leading to a high variation in median fin morphology and ontogeny. In this study, the development of anal and dorsal fins in atheriniforms is described and its consequences for the current phylogenetic hypothesis are discussed. Developmental series of five atheriniform species were investigated using clearing and staining as well as antibody staining. The skeletal elements of the second dorsal fin and the anal fin emerge in a bidirectional pattern. The first dorsal fin, however, arises separately in front of the second dorsal fin after this one is almost completely formed. The pterygiophores of the first dorsal fin, including the interdorsal pterygiophores, develop from caudal to rostral, but the fin‐spines of the first dorsal fin form in the opposite direction. This new mode of fin development has been found in all examined atheriniform species with two dorsal fins. Several morphological characters of atheriniforms, including interdorsal pterygiophores, are also found in one other taxon: the Mugiliformes. Thus, several dorsal fin characteristics may provide evidence for a closer relationship of these two taxa.     

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。     

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.     

Larval development of Hypsophrys nicaraguensis (Pisces: Cichlidae) under laboratory conditions

The cichlid Hypsophrys nicaraguensis is a popular fish known as butterfly, and despite its widespread use as pets, little is known about its reproductive biology. In order to contribute to this knowledge, the study describes the relevant larval development characteristics, from adult and larval cultures in captivity. Every 12h, samples of larvae were collected and observed under the microscope for larval stage development, and every 24h morphometric measurements were taken. Observations showed that at 120h, some larvae had swimming activity and the pectoral fins development was visible; at 144h, the dorsal fin appear and all larvae started food intake; at 168h, the formation of anal fins begins, small rudiments of pelvic fins emerge, the separation of caudal fin from anal and dorsal fins starts, and the yolk sac is reabsorbed almost completely; at 288h, the pelvic fins starts to form; at 432h, the rays and spines of dorsal and anal fins can be distinguished, both the anal and the dorsal fins have the same number of spines and rays as in adults. After 480h larvae have the first scales, ending the larval stages and starting the transformation to fingerlings. Larvae were successfully fed with commercial diet.     

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.     

Neolumpenus unocellatus,a new genus and species of stichaeid fish from Japan

Neolumpenus unocellatus gen. et sp. nov., a stichaeid fish (subfamily Lumpeninae,sensu Makushok, 1958) is described on the basis of a single specimen found in the stomach of the Pacific cod,Gadus macrocephalus Tilesius, caught off Akkeshi, Hokkaido, Japan. The new genus and species is distinguished from all other lumpenines in having the following combination of characters: 1) 51 dorsal spines, 33 anal fin rays, 57 total vertebrae; 2) broad pelvic fin with deeply-branched soft rays; 3) lower rays of pectoral fin branched and not prolonged backward; 4) prevomerine and palatine teeth present; 5) pungent spines present in pelvic and anal fins; 6) upper lip fused to snout anteriorly; 7) gill openings not extending forward beyond a vertical through posterior margin of eye; 8) minimal (fifth) hypural present; 9) first interneural spine inserted between first and second neural spines; 10) extremely large cephalic sensory pores present; 11) high, steep snout; 12) ocellus on dorsal base of caudal fin.     

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     

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.     

The origins of adipose fins: an analysis of homoplasy and the serial homology of vertebrate appendages

Adipose fins are appendages found on the dorsal midline between the dorsal and caudal fins in more than 6000 living species of teleost fishes. It has been consistently argued that adipose fins evolved once and have been lost repeatedly across teleosts owing to limited function. Here, we demonstrate that adipose fins originated repeatedly by using phylogenetic and anatomical evidence. This suggests that adipose fins are adaptive, although their function remains undetermined. To test for generalities in the evolution of form in de novo vertebrate fins, we studied the skeletal anatomy of adipose fins across 620 species belonging to 186 genera and 55 families. Adipose fins have repeatedly evolved endoskeletal plates, anterior dermal spines and fin rays. The repeated evolution of fin rays in adipose fins suggests that these fins can evolve new tissue types and increased structural complexity by expressing fin-associated developmental modules in these new territories. Patterns of skeletal elaboration differ between the various occurrences of adipose fins and challenge prevailing hypotheses for vertebrate fin origin. Adipose fins represent a powerful and, thus far, barely studied model for exploring the evolution of vertebrate limbs and the roles of adaptation and generative biases in morphological evolution.     

New genus and species of the family stichaeidae from Hokkaido,Japan

Specimens of a new genus and species of the stichaeid fish,Leptostichaeus pumilus, were collected from the Okhotsk Sea off Hokkaido in Japan. The present new genus and species clearly differs from all the other genera and species of the stichaeid fishes in the following characters: 3 or 4 pectoral fin rays; 10 or fewer caudal principal rays; 79–82 dorsal spines; no pelvic fin; last interneural spine supporting a single dorsal spine; infraorbital, occipital and lateral line canals absent; moderate size of dorsal spine shorter than eye diameter; membranes of dorsal and anal fins widely connected with caudal fin; a large black spot divided by a yellow band present just above gill cover.     

Leis' conundrum: homology of the clavus of the ocean sunfishes. 2. Ontogeny of the median fins and axial skeleton of Ranzania laevis (Teleostei, Tetraodontiformes, Molidae)

One of the most conspicuous characters of the ocean sunfishes, family Molidae, is the punctuation of the body by a deep, abbreviated, caudal fin-like structure extending vertically between the posterior ends of the dorsal and anal fins, termed the clavus by Fraser Brunner. Homology of the clavus has been a matter of debate since the first studies on molid anatomy in the early 1800s. Two hypotheses have been proposed: 1) It is a highly modified caudal fin; 2) It is formed by highly modified elements of the dorsal and anal fins. To resolve this homology issue, we studied the ontogeny of the molid vertebral column and median fins and compared it to that of a less morphologically derived gymnodont (see Part 1 of this study), a member of the family Tetraodontidae. We show that in molids the chorda never flexes during development, that the claval rays form from the posterior ends of the dorsal and anal fins toward the middle, thus closing the gap inward, and that elements of the molid clavus have an identical development and composition as the proximal-middle and distal radials of the regular dorsal and anal fins. We thus conclude that the molid clavus is unequivocally formed by modified elements of the dorsal and anal fin and that the caudal fin is lost in molids.     

记比耶鱼(Birgeria)在中国的首次发现

记述了采自云南罗平晚三叠世法郎组竹杆坡段的比耶鱼一新种──刘氏比耶鱼（Ｂｉｒｇｅｒｉａ ｌｉｕｉ ｓｐ． ｎｏｖ．）,这是比耶鱼化石在中国的首次发现。刘氏比耶鱼与产自瑞士圣乔治山中三叠世边境沥青层的史氏比耶鱼最为相近,两者仅在尾柄长高之比、尾鳍长短与上下叶外缘交角、背鳍和臀鳍辐状支鳍骨的数目、臀鳍辐状骨骨板的大小、以及侧线管骨化与否等特征上略有差异。比耶鱼与软骨硬鳞鱼超目的鲟形目最为接近,两者共有一系列特征,如除尾上叶外体侧裸露,副蝶骨末端伸达头后,鳃盖骨退化;但比耶鱼同时也具有不少的特有特征,代表了软骨硬鳞鱼超目的另一类群──比耶鱼目（Ｂｉｒｇｅｒｉｉｆｏｒｍｅｓ　ｏｒｄ． ｎｏｖ．）。刘氏比耶鱼的发现进一步表明华南扬子区中、晚三叠世鱼类化石与特提斯西部的鱼群具有密切的动物地理关系。     

Revision of Iquius nipponicus Jordan 1919 (Teleostei: Cyprinidae) from the Miocene of Iki Island, Nagasaki, Japan and its phylogenetic position

Iquius nipponicus Jordan 1919 was described on the basis of a single specimen from the Miocene of Iki Island, Nagasaki, Japan, and was tentatively assigned to the family Clupeidae. The holotype consists of the anterior portion of the body (lacking the anal and caudal fins and most of the caudal vertebrae), and is re-examined. The species is re-described based on additional specimens from the type locality. This species possesses an extremely stout third dorsal spine-like fin ray with a smooth posterior edge, an expanded anterior portion of the maxilla covering approximately half of the bone, 13 branched anal fin rays, and 22 abdominal and 16 caudal vertebrae. A phylogenetic study using the character matrix from a previous study suggests that the species forms a clade with xenocyprinins, but it differs from xenocyprinins in the form of the maxilla and the dentary and the numbers of branched anal fin rays and vertebrae. The present study concludes that the genus Iquius does not belong to the family Clupeidae. Iquius is a distinct and valid genus that is closely related to cultrins and xenocyprinins of the family Cyprinidae.     

Description of a new cryptic,shallow‐water tonguefish (Pleuronectiformes: Cynoglossidae: Symphurus) from the western North Pacific Ocean

Combined results based on morphological characters and analyses of partial sequences of the 16s rRNA and coI genes confirm the validity of a new, cryptic, symphurine tonguefish from the western North Pacific Ocean. Symphurus leucochilus n. sp., a diminutive species reaching sizes to c. 67 mm standard length, is described from nine specimens that were collected from fish‐landing ports and from trawls made at c. 150 m off Taiwan and Japan. Symphurus leucochilus shares many similar features with those of Symphurus microrhynchus and that of several undescribed species that are morphologically similar to S. microrhynchus. Symphurus leucochilus has also been misidentified as Symphurus orientalis in fish collections because of shared similarities in some aspects of their morphology. The new species differs from all congeners by the following combination of meristic, morphological and pigmentation features: a predominant 1–2–2–2–2 pattern of interdigitation of proximal dorsal‐fin pterygiophores and neural spines; 12 caudal‐fin rays; 89–92 dorsal‐fin rays; 76–80 anal‐fin rays; 49–51 total vertebrae; four hypurals; 75–83 longitudinal scale rows; 32–35 transverse scales; 15–17 scale rows on the head posterior to the lower orbit; absence of a fleshy ridge on the ocular‐side lower jaw and a membranous connection between the anterior nostril and lower part of the eye; a narrow interorbital space and dorsal‐fin origin anterior to the vertical through the anterior margin of the upper eye; absence of both dermal spots at bases of anterior dorsal‐fin rays and melanophores on the isthmus; uniformly yellow to light‐brown ocular‐side colouration without bands; dorsal and anal fins with alternating series of dark rectangular blotches and unpigmented areas; a uniform white blind side and a bluish‐black peritoneum. Despite overall similarities in morphology between S. leucochilus and S. orientalis, as well as between two of the nominal species morphologically similar to S. microrhynchus, analyses of partial 16s rRNA and coI gene sequences show that S. leucochilus, S. orientalis and the two other nominal species represent three distinct lineages within the genus Symphurus.