Ventilation of the gills by the pectoral fins in the fangtooth Anoplogaster cornutum: how to breathe with a full mouth

The midwater fangtooth Anoplogaster cornutum eats large prey items whole. To eat prey the fish distends the opercula and spreads the gill arches apart. The pectoral fins are then used to fan water over the gills until ingestion is completed.     

Pectoral fin size in a fish species with paternal care: a condition-dependent sexual trait revealing infection status

1. The three-spined stickleback, Gasterosteus aculeatus L., is a territorial fish with exclusive male parental care. Males oxygenate the eggs with fanning movements of their pectoral fins. The present authors investigated whether the apparent sexual differences in the functional demands of the pectoral fins have resulted in sexual differences in fin size. If males have relatively larger pectoral fins, females may use this as a signal to aid their mate choice for good fathers. Therefore, further objectives were to study the condition-dependency of relative pectoral fin size in males and the relationship with male parasite load. 2. Reproductively active males possessed relatively larger pectoral fins than females in both wild-caught and laboratory-bred fish. 3. In the field, caring males with relatively large pectoral fins were in better physical condition and had more food in their stomachs. 4. Relatively small pectoral fins and poor body condition were associated with infection by the intestinal parasite Pomphorhynchus laevis (Acanthocephala), the prevalent parasite species in the study population.     

Morphological evidence for the biological role of caniniform teeth in combtooth blennies (Blenniidae, Teleostei)

Combtooth blennies have recurved, fang-like caniniform teeth at the rear end of a single row of incisiform teeth. The lengths and positions of these canines were measured in the lower jaws of males of 14 species of Mediterranean Blenniidae. In four species, lower jaw canines were measured in males and females, while in one species, the upper jaw canines of both sexes were also measured. Relative (to body length) canine length in males tends to be significantly greater (10–40%) than in females. There are significant interspecific differences in relative canine length, with smaller species tending to have relatively larger teeth. No significant correlation was obtained between canine length and importance of animal prey in the diet, nor with 'hole fit' of males, which may be related with the intensity of paternal care. We suggest that canines in combtooth blennies are predominately used for predator deterrence and agonistic interactions.     

Growth dynamics of caudal and pectoral fin muscle fibres in a carangid, Caranx malabaricus (Cuv. & Val.), and their possible relation with somatic growth

The growth dynamics of red, pink and white fibres of the caudal and pectoral fin muscles are described in Carans malabaricus (Cuv. & Val.) in relation to their somatic growth. In all three fibre types growth occurred by an increase in fibre number and diameter in small size classes of fish and by an increase in diameter only in larger fish. The growth dynamics of the three fibre types were similar to those of the myotomal muscle fibres and paralleled the somatic growth pattern of this fish.     

Bergmann ecogeographic trends among triplefin blennies (Teleostei: Tripterygiidae) in the Gulf of California,Mexico

Synopsis Bergmann-type ecogeographic patterns are common among small resident rocky-shore fishes in the Gulf of California where triplefin blennies (Tripterygiidae) represent a significant component of the community. Using estimates of adult body size from samples throughout the Gulf, four triplefin species, three more than previously reported, showed significant correlations of body size with latitude. The intensity and form of the relationships are given. Measuring the length of the largest individual in samples rather than using average body weight per individuals in samples offers a better estimate of adult body size.     

Diversification of the pectoral fin shape in damselfishes (Perciformes, Pomacentridae) of the Eastern Pacific

Fin shape strongly influences performance of locomotion across all swimming styles. In this study, we focused on the diversity of the pectoral fin morphology in damselfishes of the Eastern Pacific. Underwater observations and a review of literature allowed the characterization of ten behavioral groups. Territorial and non-territorial species were discriminated easily with traditional morphometrics. Five ecomorphological groups were recognized by geometric morphometric analyses. Geometric data segregated the outgroup from the damselfishes and allowed the distinction of mean morphologies from extreme ones within territorial and non-territorial species. Additionally, geometric morphometric data split Abudefduf into two groups: (1) A. troschelii is similar to C. atrilobata and (2) A. concolor and A. declivifrons are close to Stegastes. Solitary territorial species (e.g., Stegastes) show rounded and high fins whereas non-territorial species living in groups (e.g., Chromis) present long and curved pectoral fins. In the range of morphological variation, the morphologies of Microspathodon (elongate with highly curved hydrodynamic trailing edge) and Azurina (long, slender and angular) represent the extreme morphologies within territorial and non-territorial species, respectively. Our study revealed a strong relationship between the pectoral fin shape and the behavioral diversification in damselfishes.     

A comment on the earliest spalacinae (rodentia,Muroidea)

According to F. M. Catzefliset al. (Trends Ecol. Evol. 7, 122–126, 1992), comparative dating of the oldest dichotomy in the muroid group (Spalacinae-other Muridae) by molecular and paleontological time scales produces conflicting results. For the earliest Spalacinae they refer to a date of 25–37 Ma; however, it has been demonstrated thatRhizospalax is not a muroid rodent, and a review of the record of fossil Spalacinae suggests that paleontological and molecular dating produces a comparable age (±19 Ma).     

Vascularization of the osteostracan and antiarch (Placodermi) pectoral fin: similarities, and implications for placoderm relationships

Phylogenetic analyses frequently resolve the extinct group Placodermi at the base of the clade of jawed fishes (traditionally known as the Gnathostomata), with the jawless fish group Osteostraci as sister taxon to this clade. Both gnathostomes and osteostracans possess pectoral fins supported by a radial(s) articulating on a cartilaginous scapulocoracoid. Blood vessels and nerves pass by or through the scapulocoracoid to supply the musculature of the pectoral fin, and in the Osteostraci also pass through the postbranchial lamina backing the gill chamber before reaching the scapulocoracoid. This course also characterizes the placoderm group Antiarchi. Other placoderms retain the condition typical of other jawed fishes in which the scapulocoracoid, as well as the subclavian veins and arteries, are entirely posterior to the back wall of the gill chamber, lying within the internal region of the trunkshield. These observations suggest that these placoderm groups are more closely related to other jawed fishes than are the Antiarchi, challenging the monophyly of the Placodermi.     

Unusual testicular accessory organs, the testicular blind pouches of blennies (Teleostei, Blenniidae). Fine structure, (enzyme-) histochemistry and possible functions

The testicular blind pouches (TBPs) of Lipophrys canevae and Solaria pavo have an annual reproductive cycle with an active secretion phase during spawning, a regression phase correlated with necrotic processes during post-spawning, an inactive regeneration phase during inter-spawning and prespawning. As revealed by fine structure and enzyme-histochemistry the TBPs of L. canevae and S. pavo are involved in the production of steroid glucuronides, which possibly act as pheromones, Further functions are in the secretion of small amounts of sialomuciri and in lytic activity.     

Eleven polymorphic microsatellite markers for paternity analysis in the pectoral sandpiper,Calidris melanotos

Eleven polymorphic microsatellite markers were isolated for the pectoral sandpiper, Calidris melanotos. The number of alleles observed in a sample of 149 presumably unrelated adults ranged from nine to 23 with an observed heterozygosity ranging from 0.79 to 0.92. The set of markers described here will prove useful for accurately determining paternity and therefore elucidate the hitherto unknown mating system of this species. We also report on cross‐species amplification of these markers in the semipalmated sandpiper, Calidris pusilla.     

Ontogeny of the epicranial portion of the dorsal fin in Solea solea and Scophthalmus maximus (Teleostei, Pleuronectiformes)

A study of laboratory-reared larvae of Solea solea (Soleidae) and Scophthalmus maximus (Scophthalmidae) indicated that the epicranial portion of the dorsal fin results from the anterior displacement of proximal pterygiophores during ontogeny. The adult epicranial formula is attained early during ontogeny, and the anterior displacement is finalized after the passage of the migrating eye. In both species, the first two proximal pterygiophores fuse to form an erisma that is particularly long and well-developed in Solea. Moreover, in Solea, the neural spine of the second abdominal vertebra curves over the otic region, and the neural arch of the first vertebra remains incomplete. Received: August 3, 2000 / Revised: August 10, 2001 / Accepted: October 12, 2001     

Development of the vasculature of the pectoral fin in the Australian lungfish, Neoceratodus forsteri

The development of the vasculature of the pectoral fin in the Australian lungfish, Neoceratodus forsteri, was studied by the dye-injection method. Only a single primitive subclavian artery appears from the dorsal aorta for the fin anlage, and it passes laterally through the postaxial region of the structure. The venous channel draining into the posterior cardinal vein is located in the preaxial region medially. As development proceeds, the arteriovenous arrangement in the pectoral fin anlage changes as follows: 1) one artery and one venous plexus, 2) two arteries and one vein, 3) three arteries and one vein, 4) four arteries and one vein, 5) three arteries and two veins, and 6) two arteries (radial and ulnar) and three veins (radial, ulnar, and ulnar marginal). The fin anlage through embryonic first rotation has gradually changed its postaxial margin to face dorsally and its preaxial margin to face ventrally. The second rotation causes the original preaxial margin to become dorsal and the original postaxial margin to become ventral. As a result, the radial and ulnar arteries are observed in the dorsal and ventral regions, respectively, in the medial side of the fin instead of in the lateral side as seen in the previous stage.     

Alteration of pectoral fin nerves following ablation of fin buds and by ectopic fin buds in the Japanese medaka fish

The role of the pectoral fin bud for outgrowth by fin axons was assessed by ablation of pectoral fin buds and by transplantation of fin buds to ectopic sites in the embryos of the Japanese medaka fish (Oryzias latipes). Normally nerves from segments 1-4 (S1-4) and less frequently the S5 nerve converged at the base of the fin bud by extending toward the fin bud on the ventral surface of the axial muscles (H. Okamoto and J. Y. Kuwada, 1991, Dev. Biol. 146). Following ablation of the fin bud before motor growth cones have begun to extend laterally, nerves in S1-5 followed a trajectory down the middle of each segment parallel to the borders of the metamerically arranged axial muscles rather than converging. This trajectory was similar to that of more posterior segmental nerves which do not converge toward the fin bud. When fin buds were transplanted to more posterior segments, nerves from S1-5 often changed their trajectories and extended to the base of ectopic buds. Furthermore, motor nerves from segments posterior to S5, which normally do not innervate the fin bud, also extended to the ectopic fin bud. When faced with both the host and ectopic fin bud, motor nerves extended to either fin bud or branched and extended to both fin buds. These results demonstrate that the early fin bud is necessary for correct outgrowth of fin nerves and suggest that the fin bud normally attracts fin nerves to its base. One possible mechanism for the attraction of motor growth cones by the fin bud is a long distance cue emitted by the fin bud.     

Osteopathy of the pectoral and pelvic limbs including pentadactyly in a young Kestrel (Falco t. tinnunculus)

Summary A five and a half weeks old female Kestrel exhibiting osteopathy of the pectoral and pelvic limbs, including symmetrical hyperdactyly, was investigated in order to clarify the pattern of the involved anatomical alterations and the possible causes of this developmental malformation. In the pectoral limb it consisted of a triplication of the alular digit, in the pelvic limb of a duplication of digit I. The live young Kestrel was observed for a period of two weeks to ascertain that it was unable to fly or procure prey on its own. After its death radiographs were taken and, apart from an eidonomic inspection including the wing claws, a detailed macroscopic dissection of the musculature of the pectoral and pelvic limbs was carried out using the in-water-method. Consecutive dissection steps were documented by a series of photographic slides. The relevant musculature, particularly that of the supernumerary digits, was recorded in proportional drawings. Subsequent to maceration of the limbs the isolated bones were reassembled according to the radiographs and also documented by means of photographs and drawings. This anatomical approach produced a reliable reconstruction of the skeletomuscular apparatus of the hyperdactylous limb parts. The eidonomic inspection revealed that at least young Kestrels may have two (alular and major digit) or even three wing claws per side. The proximal skeletal elements of both pectoral and pelvic limb were more sturdily built than in a typical Kestrel of comparable age. The proximal elements of the pelvic limb, the tarsometatarsus in particular, were shorter than in a typical Kestrel. In addition, the long axis of the tarsometatarsus was laterally bent in the transverse plane so that its proximal articular surfaces were medially inclined. Duplication of the cutaneous and osseous elements in the foot was accompanied by a duplication of some of the muscular and/or tendinous elements supplying digit I proper and the accessory digit I'. There were left-to-right asymmetries of the pedal musculature concerned. In contrast, the two accessory alular digits of each wing were almost completely devoid of musculature. Apart from atypical points of origin or insertion of the remaining distal musculture, left-to-right asymmetries and the two accessory alulae per wing, presumably, affected aerodynamic properties and resulted in flightlessness.A juvenile Kestrel of similar age and without hyperdactyly was dissected for comparison. In addition, the external appearance of the carpometacarpal region of two female Silkies, an obligatory pentadactylous breed of domestic fowl, was inspected and the skeletal parts of their pectoral and pelvic limbs compared with those of the hyperdactylous Kestrel. Our results and a literature review suggest that the symmetrical hyperdactyly in the Kestrel bears striking similarities to the hereditary hyperdactyly observed in certain breeds of domestic fowl. In addition, there is a striking resemblance between the hyperdactyly of the young Kestrel and certain forms of hyperdactyly induced by molecular genetical experiments of other authors on chicks. Comparison with these results taken from the literature suggest that the symmetrical hyperdactyly in the young Kestrel, including the alterations of the proximal skeletal elements, is caused by an unusually early expression of the Hoxd-11 gene group during embryological development. Most likely, this gene group is situated on the 2^nd chromosome in birds just as it is in mammals.

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Osteopathie der Vorder - und Hinterextremitäten, verbunden mit einer symmetrischen Hyperdactylie bei einem jungen Turmfalken (Falco tinnunculus)

Zusammenfassung Ein fünfeinhalb Wochen alter weiblicher Turmfalke mit einer Osteopathie der Vorder- und Hinterextremitäten, verbunden mit einer symmetrischen Hyperdactylie, wurde untersucht, um das Muster der beteiligten anatomischen Veränderungen und die möglichen Ursachen dieser Mißbildung zu erkennen. An der Vorderextremität bestand sie aus einer Verdreifachung des Alula-Fingers, an der Hinterextremität aus einer Verdoppelung der Zehe I. Die Beobachtung des lebenden jungen Turmfalken während eines Zeitraumes von zwei Wochen ergab, dass er flugunfähig war und keine Beute schlagen konnte.Nach seinem Tod und einer Inspektion der Eidonomie, einschließlich der Flügelkrallen, wurden Röntgenaufnahmen angefertigt. Danach folgte eine detaillierte makroskopische Präparation der Flügel- und Beinmuskulatur unter Verwendung der In-Wasser-Methode. Die einzelnen Präparationsschritte wurden anhand von Dia-Serien dokumentiert. Die relevante Muskulatur, insbesondere die der überzähligen Digiti, wurde in proportionsgetreuen Zeichnungen festgehalten. Nach Mazeration der Extremitäten wurden die Einzelknochen, entsprechend den Röntgenbildern, wieder zusammengesetzt und ebenfalls mit Fotografien und Zeichnungen dokumentiert. Dieser anatomische Ansatz lieferte eine zuverlässige Rekonstruktion des Skelett-Muskel-Apparates der hyperdactylen Extremitätenanteile.Die eidonomische Inspektion ergab, dass zumindest junge Turmfalken zwei (Digitus alularis und majoris) oder sogar drei Flügelkrallen haben können. Die proximalen Skelettelemente der Vorder- und Hinterextremität waren deutlich robuster gebaut als bei einem typischen Turmfalken vergleichbaren Alters. Die proximalen Elemente der Hinterextremität, insbesondere der Tarsometatarsus, waren kürzer als bei einem typischen Turmfalken. Darüberhinaus war die Längsachse des Tarsometatarsus in der Transversalebene laterad gekrümmt, so dass sich seine proximalen Gelenkflächen schräg mediad richteten. Entsprechend der kutanen und knöchernen Doppelbildungen des Fußes waren auch einige der Muskeln und Sehnen doppelt vorhanden, welche die eigentliche erste Zehe und die akzessorische erste Zehe versorgten. Es traten Rechts-/Links-Asymmetrien der betreffenden Muskulatur auf. Im Gegensatz dazu waren die beiden akzessorischen Alula-Finger jedes Flügels fast vollständig ohne Muskulatur. Abgesehen von atypischen Ursprungs- und Insertionspunkten der verbleibenden distalen Muskulatur, beeinträchtigten Rechts-/Links-Asymmetrien und die beiden akzessorischen Alulae pro Flügel vermutlich die aerodynamischen Eigenschaften und führten zur Flugunfähigkeit.Ein junger Turmfalke ähnlichen Alters ohne Hyperdactylie wurde zum Vergleich präpariert. Zusätzlich wurde die äußere Erscheinung der Carpometacarpal-Region zweier Seidenhühner, einer obligatorisch pentadactylen Hühnerrasse, inspiziert und die Skelettelemente ihrer Vorder- und Hinterextremitäten mit denen des hyperdactylen Turmfalken verglichen. Unsere Ergebnisse und ein Überblick der Literatur lassen auffallende Übereinstimmungen zwischen der symmetrischen Hyperdactylie des jungen Turmfalken und der erblichen Hyperdactylie bestimmter Hühnerrassen erkennen. Darüberhinaus besteht eine auffallende übereinstimmung zwischen der Hyperdactylie des jungen Turmfalken und bestimmten Formen der Hyperdactylie, welche von anderen Autoren durch molekulargenetische Experimente an Hühnerküken induziert wurden. Ein Vergleich mit diesen Ergebnissen aus der Literatur legt nahe, dass die symmetrische Hyperdactylie des jungen Turmfalken, einschließlich der Veränderungen der proximalen Skelettelemente, durch eine ungewöhnlich frühe Expression der Hoxd-11 Gengruppe im Laufe der Embryonalentwicklung verursacht wurde. Sehr wahrscheinlich ist diese Gengruppe bei Vögeln auf dem zweiten Chromosom lokalisiert — ebenso wie bei Säugetieren.