Early development of dorsal and pelvic fins and their supports in hatchery-reared red-spotted grouper, Epinephelus akaara (Perciformes: Serranidae)

Early morphogenesis of dorsal and pelvic fins and their supports in the larval and juvenile red-spotted grouper, Epinephelus akaara, was examined using a hatchery-reared series. The dorsal spine anlage first appeared suspended in the middle part of the finfold at ca. 2.5 mm TL. Dorsal and pelvic supports appeared by the time the fish reached ca. 3 mm and started to ossify at ca. 3.5 mm. Elongated spines and their supports developed synchronously in both dorsal and pelvic fins. The formation of dorsal fin supports proceeded from anterior to posterior. The ossification of supports was completed by ca. 33 mm. Spinelets on the second dorsal spine and pelvic spine appeared by ca. 3 mm. In specimens larger than 36 mm, all spinelets on the second dorsal spine and pelvic spine had disappeared. The maximum size of the second dorsal spine and pelvic spine lengths relative to TL were ca. 45% and 44% at 3.3 mm in fish size, respectively. Thereafter, their proportions decreased gradually. Considering the order of development of the elongated spines and mucous cells in the early life stages, the elongated spines might function as antipredator devices. Received: June 20, 2000 / Revised: April 28, 2001 / Accepted: June 11, 2001     

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.     

What do male tench, Tinca tinca, advertise with morphological ornaments?

In contrast to females, tench Tinca tinca (L.) males have large pelvic fins with a thickened and bent second fin ray. Males also produce notable ventral protuberances during breeding, but the function of these male ornaments is not known. Using wild-caught fish, we found that both the size of pelvic fins and ventral protuberance were dependent on body mass/length ratio but not necessarily on condition. Plasma testosterone concentration and relative gonad mass were positively correlated with condition factor. Plasma testosterone concentration was not related to measures of non-specific immune function, but correlated positively with the size of pelvic fins corrected for body length. However, the studied male ornaments were not related to the measures of immune defence or to the load of Diplostomum spp. We did not find evidence for male–male dominance or female preference for large male characteristics within the natural variation in these traits. Thus, our study suggests that also other mechanisms than sexual selection on good genes might contribute to the maintenance of sexual dimorphism in tench.     

Microanatomy of the paired‐fin pads of ostariophysan fishes (Teleostei: Ostariophysi)

Members of the teleost superorder Ostariophysi dominate freshwater habitats on all continents except Antarctica and Australia. Obligate benthic and rheophilic taxa from four different orders of the Ostariophysi (Gonorynchiformes, Cypriniformes, Characiformes, and Siluriformes) frequently exhibit thickened pads of skin along the ventral surface of the anteriormost ray or rays of horizontally orientated paired (pectoral and pelvic) fins. Such paired‐fin pads, though convergent, are externally homogenous across ostariophysan groups (particularly nonsiluriform taxa) and have been considered previously to be the result of epidermal modification. Histological examination of the pectoral and/or pelvic fins of 44 species of ostariophysans (including members of the Gonorynchiforms, Cypriniformes, Characiformes, and Siluriformes) revealed a tremendous and previously unrecognized diversity in the cellular arrangement of the skin layers (epidermis and subdermis) contributing to the paired‐fin pads. Three types of paired‐fin pads (Types 1–3) are identified in nonsiluriform ostariophysan fishes, based on differences in the cellular arrangement of the epidermis and subdermis. The paired‐fin pads of siluriforms may or may not exhibit a deep series of ridges and grooves across the surface. Two distinct patterns of unculus producing cells are identified in the epidermis of the paired‐fin pads of siluriforms, one of which is characterized by distinct bands of keratinization throughout the epidermis and is described in Amphilius platychir (Amphiliidae) for the first time. General histological comparisons between the paired fins of benthic and rheophilic ostariophysan and nonostariophysan percomorph fishes are provided, and the possible function(s) of the paired‐fin pads of ostariophysan fish are discussed. J. Morphol. 2012. © 2012 Wiley Periodicals, Inc.     

Chemoreception in the food-searching and feeding behavior of the red hake, Urophysics chuss (Walbaum)

Behavioral observations were made of hake, Urophycis chuss (Wa,baum), presented with a freeze-dried clam extract over a wide concentration range. The silent food searching behaviors observed were emerging from shelter, swimming, and extending the chemosensitive modified pelvic fins over the bottom. Some fish also snapped at the source of extract-laden sea water. As the extract concentration increased, the three food searching behaviors occurred in more individuals and more concurrently in the same individuals. Above 10^?9 g·1^?1, the percentage of hake showing the three food-searching behaviors and snapping increased linearly with the logarithm of the extract concentration. Detection was inferred from emergence from shelter or extension of pelvic fins. The threshold concentration at which 50% of the hake showed the behaviors indicating detection was 10^?8 g·1^?1. The thresholds for food searching and snapping were 10^?7 g·1^?1, respectively. The amounts of time spent swimming and moving the pelvic fins over the bottom were power functions of the food extract concentration. For hake, variation in one sensory input, strength of a chemical food cue, largely determined the onset and duration of food searching and feeding behavior.     

Dechlorination of high-molecular-mass compounds in spent sulphite bleach effluents by free and immobilized cells of streptomycetes

Streptomyces chromofuscus and S. rochei dechlorinated high-molecular-mass compounds (HMM) from industrial bleach effluents. Compounds of the effluents from the first chlorination [(C + D)_red] and the subsequent alkaline extraction stage (E₁O) of a sulphite cellulose pulp mill were used as substrates for the microbial transformations. HMM bleach effluent fractions obtained by ultrafiltration were treated by free and immobilized cells in two types of bioreactors. The dechlorination was followed by measuring the reduction of activated-carbon-adsorbable organic-bound halogen (AOX) and the release of inorganic chloride. While 38–45% of the organic bound chlorine was released from a mixture of (C + D)_red and E₁O stage effluents within 20 days of incubation with S. chromofuscus, only 11–16% were liberated from E₁O-stage HMM bleach-effluent compounds by S. chromofuscus and S. rochei. Immobilized cells of both strains remained active for over 100 days in successive batches, each releasing 12–24% of chloride from HMM bleach-effluent compounds.     

A new blind loach, <Emphasis Type="Italic">Oreonectes elongatus</Emphasis> sp. nov. (Cypriniformes: Balitoridae) from Guangxi,China

A new loach, Oreonectes elongatus sp. nov. is described based on collections from Mulun Township, Huanjiang County, Guangxi in China. It is distinguished from its congeners by the combination of the following characters: most elongate body (body depth/SL 8.62–10.68%), blind, a forked caudal fin, obvious adipose dorsal crest and ventral crest; entire body naked and de-pigmented. Although the new species has a similar distribution with O. macrolepis, it can be distinguished by scales (absent in O. elongatus vs. present in O. macrolepis), shape of snout (elongate vs. round), the opposite position of the dorsal and pelvic fins origins (behind vs. front). The new species shares the same possession of dorsal and ventral crests, a forked caudal fin, eyeless, naked body and incomplete lateral line with O. translucens, but can be distinguished from the latter by caudal fin crest (more developed and translucent in O. translucens), longer anterior nostril tube and barbel, extreme of pectoral fin reaching 2/3 of the distance between origin of pectoral and pelvic fins, more vertebrae (4 + 38–39 vs. 4 + 32).     

Special cutaneous receptor organs of fish. IV. Ampullary organs of the nonelectric catfish, Kryptopterus

Ampullary organs of the transparent catfish, Kryptopterus bicirrhus, are present in large numbers on the head and in a regular pattern of lines on the body and fins. The organs lie in the epidermis, and have a pore that opens to the surface. Flattened cells form a roof and walls. On the floor of the organ there are a “sensory hillock,” composed of spherical receptor cells and columnar supporting cells, and a “secretory hillock” composed of columnar secretory cells. The receptor cells are nonciliated and have only afferent innervation. The organ cavity is filled with jelly. The organs are compared with ampullary organs of the weakly electric fish Eigenmannia, ampullae of Lorenzini of Raja, and small pit organs of Amiurus. Structural characteristics of the ampullary organs of Kryptopterus make them especially suitable for electrophysiological studies.     

Asterropteryx atripes, a new gobiid fish from the Western Pacific Ocean (Perciformes: Gobioidei)

 A new gobiid fish, Asterropteryx atripes, is described on the basis of eight specimens from Iriomote-jima Island, Ryukyu Islands, and El Nido, Philippines. It differs from its congeners by having the following combination of characters: 3rd spine of first dorsal fin long, filamentous, distal tip usually over end of 2nd dorsal fin base when appressed in both sexes; pelvic fins almost separated, innermost (=5th) segmented rays connected by rudimentary low membrane between bases, and no frenum; 4–7 short spines on posterior margin of preopercle (the uppermost spine usually just behind the cephalic sensory canal pore N); eye large, 32.3–35.8% of head length; enlarged haemal arches on 1st two caudal vertebrae; a distinct black band from posterior margin of eye to caudal fin base (indistinct in dark-phase individuals); black pelvic fin (vivid in dark-phase individuals); numerous minute bright blue spots on head and body in life; no distinct dark spots on head and body; iris entirely reddish-brown or dusky (bright white ventrally in pale-phase individuals) when alive or fresh, and entirely black in preservation, without white transverse bar on middorsal surface; hovering habit. The new species appears to be most closely related with the other only known hovering species, A. striata; the latter is readily distinguished from the former in having no long, filamentous dorsal spine; semitranslucent pelvic fin; and a series of small black spots along dorsal fin base and dorsal edge of caudal peduncle. Asterropteryx contains two distinct groups, and the monophyly of the genus is open to question. Received: March 19, 2000 / Revised: February 25, 2002 / Accepted: April 25, 2002     

Adaptations for cryopelagic life in the antarctic notothenioid fish Pagothenia borchgrevinki

Summary The cryopelagic circumantarctic notothenioid fish Pagothenia borchgrevinki lives near the undersurface of the sea ice in McMurdo Sound, Antarctica. When compared to closely related benthic species (especially Trematomus bernacchii), Pagothenia exhibited substantial morphological differences in a variety of organ systems. The values of the fineness ratio and the indices of trunk shape and flatness suggested streamlining and drag reduction, adaptations to life in the water column. Pagothenia also lacked substrate contact adaptations in the pelvic and anal fins. Silvery reflective layers (strata argentea) beneath the skin and in the iris and choroid of the eye provided camouflage when Pagothenia were viewed against a background of platelet ice. The retina had many cones indicating the eye was adapted to both diurnal and nocturnal vision. During the austral spring Pagothenia fed exclusively on nektonic organisms near the ice-water interface. Dietary diversity was low; copepods and amphipods were the most frequently occurring and amphipods were the most frequently occurring taxa. In conclusion, Pagothenia appear specialized for life in the water column.     

Rineloricaria isaaci (Loricariidae: Loricariinae), a new species of loricariid catfish from the Uruguay River basin

Rineloricaria isaaci is described from tributaries of the Uruguay River basin in Argentina, Brazil and Uruguay. The new species is distinguished by having a long and wide area of naked skin at the snout tip, surpassing the anteriormost pore of the infraorbital ramus of the sensory canal, approximately in the middle of the third postrostral plate, and by its particular sexual dimorphism characterized by the long pectoral and pelvic fins of mature males.     

Allometric growth of the trunk leads to the rostral shift of the pelvic fin in teleost fishes

The pelvic fin position among teleost fishes has shifted rostrally during evolution, resulting in diversification of both behavior and habitat. We explored the developmental basis for the rostral shift in pelvic fin position in teleost fishes using zebrafish (abdominal pelvic fins) and Nile tilapia (thoracic pelvic fins). Cell fate mapping experiments revealed that changes in the distribution of lateral plate mesodermal cells accompany the trunk-tail protrusion. Presumptive pelvic fin cells are originally located at the body wall adjacent to the anterior limit of hoxc10a expression in the spinal cord, and their position shifts rostrally as the trunk grows. We then showed that the differences in pelvic fin position between zebrafish and Nile tilapia were not due to changes in expression or function of gdf11. We also found that hox-independent motoneurons located above the pelvic fins innervate into the pelvic musculature. Our results suggest that there is a common mechanism among teleosts and tetrapods that controls paired appendage positioning via gdf11, but in teleost fishes the position of prospective pelvic fin cells on the yolk surface shifts as the trunk grows. In addition, teleost motoneurons, which lack lateral motor columns, innervate the pelvic fins in a manner independent of the rostral-caudal patterns of hox expression in the spinal cord.     

Adhesion by Paired Pectoral and Pelvic Fins in a Mountain-Stream Catfish, Pseudocheneis sulcatus (Sisoridae)

We describe the adhesive nature of the pectoral and pelvic fins in the catfish Pseudocheneis sulcatus, as examined by scanning electron microscopy. The outer rays of these fins are modified into structures that bear prominent transverse ridges and grooves. The outer epidermal cells of the ridges are thrown into elongated spines. Mucous pores (openings of mucous glands) are frequently present (100m apart) in the epidermis of the ridges and show entangled mucus droplets. In the pectoral fins, they are present towards the contour areas of the outer rays, but they are absent in the pelvic fins. In the latter, mucous pores are present near the base of the ridges (distal to the inner rays). Spines as well as mucous pores are absent in the cells that line the groove between two adjacent ridges. We suggest that in this species adhesion is effected by suction pressure generated by the musculature attached to the grooves and ridges, and that mucus and the spines aid in this process.     

Does body and fin form affect the maneuverability of fish traversing vertical and horizontal slits?

Synopsis The purpose of this study was to determine if body and fin form affected the maneuverability of teleostean fishes as measured by their ability to negotiate simple obstacles. Obstacles were vertical and horizontal rectangular slits of different widths, for which width was defined as the minimum dimension of a slit irrespective of slit orientation. Performance was measured as the smallest slit width traversed. Three species with different body and fin patterns were induced to swim through slits. Species tested were; goldfish Carassius auratus with a fusiform body, anterio-ventral pectoral fins and posterio-ventral pelvic fins; silver dollars Metynnis hypsauchen with the same fin configurations but a gibbose body; angelfish Pterophyllum scalare with a gibbose body and anterio-lateral pectoral fins. Minimum slit widths negotiated were normalized with the length of various body dimensions: total length, maximum width, span at the pectoral fins, and volume^1/3 (numerically equal to mass^1/3). Goldfish had the poorest performance, requiring the largest slit widths relative to these body dimensions. No consistent patterns in performance were found for silver dollars vs. angelfish. There were no differences among species in the ratio of minimum vertical slit width negotiated to that for horizontal slits, indicating fish were equally able to control posture while swimming on their sides. There were also no consistent patterns in the times taken to transit slits. Although the deep-bodied fish were able to maneuver through smaller slits, the most striking result is the similarity of minimum slit widths traversed in spite of the large variation in body form. Body form and fin plan may be more important for maneuvering and posture control during sub-maximum routine activities.     

Does fin damage allow discrimination among wild,escaped and farmed Sparus aurata (L.) and Dicentrarchus labrax (L.)?

The present study compares fin damages in gilthead seabream (Sparus aurata) and European seabass (Dicentrarchus labrax) according to their wild, escaped or farmed origins. In addition, the potential applicability of fin condition indices (Fin Erosion Index ‘FEI’ and Fin Splitting Index ‘FSI’) as identification tools is discussed. Farmed seabream fins evidenced more erosion and splitting (FEI ± SD: 2.1 ± 0.3; FSI ± SD: 1.9 ± 0.6) than wild seabream fins (FEI: 0.8 ± 0.6; FSI: 1.2 ± 0.9), a result of farming conditions in open‐sea cages. Escaped seabream fin erosion was between that of farmed and wild seabream (FEI: 1.6 ± 0.4), which could indicate that fins in farmed fish recover over time from farming abrasions once they are in the wild. However, the fins of escaped seabream seem to be weaker than those of the wild fish, and therefore might be more susceptible to suffer other types of erosion such as splitting or nipping (FSI: 2.3 ± 0.7). No significant differences were found in seabass FEI according to their origins, although wild seabass presented significantly more split caudal fins (FSI: 3.3 ± 2.8) than the farmed seabass (FSI: 1.2 ± 1.1) and escapees (FSI: 2.5 ± 1.6). Therefore, FEI for seabream could be used as tools not only to distinguish between wild and farmed fish, but also to identify recent escapees, improving further assessments on the contribution of seabream escapees in fishery landings. However, the healing potential of damaged fins must be considered for the proper identification of escapees. Use of fin condition indices from both species could be helpful for aquaculture management, to assess fish welfare in fish farms stocks, and improve the knowledge of handling, stock densities and open‐sea cage environment conditions.     

A microanatomical and histological study of the fin long bones of the Devonian sarcopterygian Eusthenopteron foordi

Meunier F.J. and Laurin M. 2012. A microanatomical and histological study of the fin long bones of the Devonian sarcopterygian Eusthenopteron foordi. —Acta Zoologica (Stockholm) 93 : 88–97. A paleohistological study of the endoskeletal bones of the dorsal and pelvic fins shows that Eusthenopteron foordi had true long bones that grew in length and thickness through endochondral and periosteal ossification, respectively. Endochondral ossification required cartilaginous epiphyses with a growth plate system whose presence is confirmed by both calcified cartilage and thin endochondral bony trabeculae that overlaid the erosive bays located in hypertrophic calcified cartilage. Articulations between axial mesomeres in paired fins were diarthroses. This microanatomical organization, i.e. longitudinal growth of diaphysis and articulations between epiphyses, can be considered an exaptation for terrestrial locomotion as it can produce skeletal elements able to support strong mechanical stress.     

The Fish Swimming Trace Undichna from the Mississippian Mauch Chunk Formation,Eastern Pennsylvania

Undichna, the swimming trace of fish, was recovered from the middle member of the Mauch Chunk Formation in eastern Pennsylvania in strata of Late Mississippian (Visean) age. These traces represent the only evidence of fish known from the Mauch Chunk Formation and the Carboniferous of Eastern Pennsylvania. The Mauch Chunk Formation in the study area is characterized by an ephemeral fluvial depositional environment that yields a diverse invertebrate ichnoassemblage of the Scoyenia ichnofacies and a tetrapod footprint assemblage dominated by the tracks of temnospondyl amphibians. The Undichna specimens are preserved on fine-grained, mudstone-draped, rippled sandstone. Two specimens, assigned to U. Britannica, consist of pairs of well-defined, narrowly incised, sinusoidal wave traces that are out-of-phase. Two specimens, assigned to U. quina, consist of two pairs of in-phase sinusoidal waves intersected by an additional single wave with a greater amplitude. Two specimens, each composed of a single wave, are assigned to U. unisulca.

The slabs of rock with the Undichna traces also preserve tetrapod undertracks assigned to Batrachichnus, Matthewichnus, and Hylopus. This trace fossil association indicates the presence of small fish, some with caudal and/or anal fins and some with pectoral, pelvic, and anal and/or caudal fins, that touched the sediment during periods of intermittent flooding of subaerial surfaces walked upon by early tetrapods. Examples of Undichna from Mississippian or older deposits, especially from a fluvial paleoenvironment, are rare; few have been reported from the Devonian and the Lower Carboniferous.     

The morphology of the adhesive organ of the sisorid fish,Glyptothorax pectinopterus

In the sisorid fish,Glyptothorax pectinopterus, the adhesive organ located on the ventral side of the thorax consists of a number of longitudinal ridges and grooves that alternate with each other around a triangular furrow lying in the centre. Adhesion of the fish to the rocky substratum in a hill stream habitat is brought about by the hooked and keratinized epidermal spines borne by the longitudinal ridges of the adhesive organ as well as those on the under surface of the pectoral and pelvic fins. The secretion of a surface coat of mucopolysaccharides by the mucous cells and the goblet cells is a device to protect the adhesive organ from mechanical abrasion.     

Anatomical network analysis of the musculoskeletal system reveals integration loss and parcellation boost during the fins‐to‐limbs transition

Tetrapods evolved from within the lobe‐finned fishes around 370 Ma. The evolution of limbs from lobe‐fins entailed a major reorganization of the skeletal and muscular anatomy of appendages in early tetrapods. Concurrently, a degree of similarity between pectoral and pelvic appendages also evolved. Here, we compared the anatomy of appendages in extant lobe‐finned fishes (Latimeria and Neoceratodus) and anatomically plesiomorphic amphibians (Ambystoma, Salamandra) and amniotes (Sphenodon) to trace and reconstruct the musculoskeletal changes that took place during the fins‐to‐limbs transition. We quantified the anatomy of appendages using network analysis. First, we built network models—in which nodes represent bones and muscles, and links represent their anatomical connections—and then we measured network parameters related to their anatomical integration, heterogeneity, and modularity. Our results reveal an evolutionary transition toward less integrated, more modular appendages. We interpret this transition as a diversification of muscle functions in tetrapods compared to lobe‐finned fishes. Limbs and lobe‐fins show also a greater similarity between their pectoral and pelvic appendages than ray‐fins do. These findings on extant species provide a basis for future quantitative and comprehensive reconstructions of the anatomy of limbs in early tetrapod fossils, and a way to better understand the fins‐to‐limbs transition.