Ontogeny of the maxillary barbel muscles in Clarias gariepinus (Siluroidei: Clariidae), with some notes on the palatine-maxillary mechanism

Siluroids are characterized by the presence of a palatine-maxillary mechanism, which enables a controlled mobility of the maxillary barbels. In Clarias gariepinus , the ontogeny of this mechanism is studied and described as well as those muscles related to the maxillary barbel. Two muscles are distinguished: (1) retractor tentaculi , connecting the maxilla to the suspensorium, and (2) extensor tentaculi , running from the ventro-lateral face of the skull to the posterior half of the palatine. These typical catfish muscles are derived from muscles that are present in generalized teleost fishes. The retractor muscle is believed to be derived from the A₃ muscle of the adductor mandibulae complex. The extensor muscle is formed from the anterior fibres of the adductor arcus palatini. The palatine is rod-like in C. gariepinus and articulates with the orbitonasal lamina in larval specimens and with its ossification, the lateral ethmoid, in juvenile and adult specimens. The articulation occurs via a long cartilaginous strip on the dorsal face of the autopalatine, thereby enabling both a rotation and a restricted sliding.     

Comparative anatomy of the cheek muscles within the Centromochlinae subfamily (Ostariophysi, Siluriformes, Auchenipteridae)

Glanidium melanopterum Miranda Ribeiro, a typical representative of the subfamily Centromochlinae (Siluriformes: Auchenipteridae), is herein described myologically and compared to other representative species within the group, Glanidium ribeiroi, G. leopardum, Tatia neivai, T. intermedia, T. creutzbergi, Centromochlus heckelii, and C. existimatus. The structure of seven pairs of striated cephalic muscles was compared anatomically: adductor mandibulae, levator arcus palatini, dilatator operculi, adductor arcus palatini, extensor tentaculi, retractor tentaculi, and levator operculi. We observed broad adductor mandibulae muscles in both Glanidium and Tatia, catfishes with depressed heads and smaller eyes. Similarities between muscles were observed: the presence of a large aponeurotic insertion for the levator arcus palatini muscle; an adductor arcus palatini muscle whose origin spread over the orbitosphenoid, pterosphenoid, and parasphenoid; and the extensor tentaculi muscle broadly attached to the autopalatine. There is no retractor tentaculi muscle in either the Glanidium or Tatia species. On the other hand, in Centromochlus, with forms having large eyes and the tallest head, the adductor mandibulae muscles are slim; there is a thin aponeurotic or muscular insertion for the levator arcus palatini muscle; the adductor arcus palatini muscle originates from a single osseous process, forming a keel on the parasphenoid; the extensor tentaculi muscle is loosely attached to the autopalatine, permitting exclusive rotating and sliding movements between this bone and the maxillary. The retractor tentaculi muscle is connected to the maxilla through a single tendon, so that both extensor and retractor tentaculi muscles contribute to a wide array of movements of the maxillary barbels. A discussion on the differences in autopalatine-maxillary movements among the analyzed groups is given.     

Ontogeny of the hyoid musculature in the African catfish, Clarias gariepinus (Burchell, 1822) (Siluroidei: Glariidae)

Three ontogenetic stages of the African catfish Clarias gariepinus have been used to describe and discuss the ontogeny of the hyoid musculature. During ontogeny, an asynchrony in the development of the muscles is observed: the intermandibularis and protractor hyoidei are the first to develop and which bear their insertions, followed by the hyohyoideus inferior and the sternohyoideus. The hyohyoideus abductor and adductor muscles are the last of the hyoid muscles to develop. In the juvenile stage (136.2 mm SL specimen), the intermandibularis is still present. The protractor hyoidei is well developed, as it may play an important role in the opening of the mouth, the elevation of the hyoid bars and, as a typical catfish feature, the displacement of the mandibular barbels. The protractor hyoidei arises as three pairs of muscle bundles (a pars ventralis, a pars lateralis and a pars dorsalis), of which the pars ventralis and the pars lateralis become fused to each other. This fusion gives rise to four different fields of superficial fibres for the manipulation of the mandibular barbels. The pars dorsalis, with its tendinous insertion, may be of more importance for mouth opening and/ or hyoid elevation. The hyohyoid muscle is well differentiated into an inferior, abductor and adductor muscles, acting on the hyoid bars, the branchiostegal rays and the opercular bone.     

Ontogeny of the jaw and maxillary barbel musculature in the armoured catfish families Loricariidae and Callichthyidae (Loricarioidea,Siluriformes), with a discussion on muscle homologies

The neotropical loricarioid catfishes include six families, the most species‐rich of which are the Callichthyidae and the Loricariidae. Loricariidae (suckermouth armoured catfishes) have a highly specialized head morphology, including an exceptionally large number of muscles derived from the adductor mandibulae complex and the adductor arcus palatini. Terminology of these muscles varies among the literature, and no data exist on their ontogenetic origin. A detailed examination of the ontogeny of both a callichthyid and a loricariid representative now reveals the identity of the jaw and maxillary barbel musculature, and supports new hypotheses concerning homologies. The adductor mandibulae muscle itself is homologous to the A1‐OST and A3′ of basal catfishes, and the A3′ has given rise to the newly evolved loricariid retractor veli as well. The A2 and A3″ have resulted in the retractor tentaculi of Callichthyidae and the retractor premaxillae of Loricariidae. Thus, these two muscles are shown to be homologous. In Loricariidae, the extensor tentaculi consists of two separate muscles inserting on the autopalatine, and evidence is given on the evolutionary origin of the loricariid levator tentaculi (previously and erroneously known as retractor tentaculi) from the extensor tentaculi, and not the adductor mandibulae complex. © 2009 The Linnean Society of London, Zoological Journal of the Linnean Society, 2009, 155 , 76–96.     

Polymorphism of white muscle myosin and parvalbumins in the genus Barbus (Teleostei: Cyprinidae)

Muscle proteins were investigated in two large European barbels, Barbus barbus and B. meridionalis , and in four small tropical barbels native to SE Asia: B. conchonius , B. tetrazona , B. sachsi and B. titteya . Polyacrylamide gel electrophoresis was used to analyse myosin heavy and light chains and parvalbumin isotypes from white trunk muscle. Each species could be biochemically identified. The myosin subunit and parvalbumin isotype patterns obtained for the two European barbels were similar. The Asian barbels, on the other hand, not only differed from the European species but displayed a greater diversity within their group. These biochemical results are largely in agreement with morphological and genetic data, but fail to substantiate suggested close relationships between Asian barbel species.     

Electrophoretic comparison of myosin light chains and parvalbumins of trunk and head muscles from two barbel (Barbus barbus) populations

• 1.1. Myosin light chains and parvalbumins have been compared in several trunk and head muscles from small and large size barbels (Barbus barbus) living in river or reared in hatchery.
• 2.2. These proteins isolated from white, red and ventricle fibres exhibit identical electrophoretic characteristics in the four batches.
• 3.3. The slow fibre content and the parvalbumin distribution are generally similar in river and hatchery barbels of the same size but differ between small and large barbels within a population.
• 4.4. Alterations of the mode of fertilization and breeding conditions do not modify the differentiation of myosin and parvalbumins in barbels.

     

Structure of tendon organs in fishes of the genus Polymixia

Summary Modified branchiostegal rays 1 through 3 support the proximal end of the paired hyoid barbels in the beardfish (Beryciformes: Polymixiidae). The polymixiid barbel is unusual in that it has an unique intrinsic muscular system. Using silver impregnation and electron microscopic techniques, unencapsulated, free nerve endings were located within the tendon of the third modified branchiostegal ray. Branchiostegal rays 1 and 2 do not have any free nerve endings associated with their tendons, however. It is suggested that the free nerve endings are proprioceptors acting as stretch-sensitive mechanoreceptors, and that branchiostegal ray 3 acts as part of a sensory apparatus for monitoring the positional state of the barbel. Branchiostegal rays 1 and 2 merely provide support for the barbel.Abbreviations used in Figures BA barbel - br r 3 branchiostegal ray 3 - IM intermandibularis - IOP interoperculum - LIM interoperculomandibular ligament - MD mandible - MX maxilla - OP operculum - PM premaxilla - POP preoperculum - SOP suboperculum     

The venous system of the terrestrial crab Ocypode cordimanus (Desmarest 1825) with particular reference to the vasculature of the lungs

The respiratory system of Ocypode cordimanus consists of seven pairs of gills, modified for aerial gas exchange, and a single pair of lungs. Each lung is formed from the inner surface of the branchiostegite and the thoracic wall of the branchial chamber. The branchiostegal surface is increased by a fleshy infolding, the branchiostegal shelf, whilst the surface area of the thoracic lung wall is enhanced by a large flaplike fold. The anatomy of the major sinus systems and the vascular supply to the lungs were investigated. Venous hemolymph is supplied to the lungs potentially from all the major body sinuses. The dorsal, ventral, hepatic, and infrabranchial sinuses are all connected anteriorly to the two eye sinuses which distribute hemolymph to the lungs. Each eye sinus gives off five branches to the branchiostegal lung surface and one to the thoracic lung wall. These afferent vessels are highly branched and interdigitate closely with efferent vessels. The two systems are connected by flat lacunae lying just beneath the respiratory epithelium and these are believed to be the site of gas exchange. The efferent vessels empty into two pulmonary veins on each side, one serving the branchiostegal lung wall and the other the thoracic wall. The two vessels on each side fuse before joining the pericardial cavity as a single trunk on each side.     

Porocottus leptosomus sp. nov., from the west coast of Korea, Yellow Sea (Scorpaeniformes: Cottidae)

 A new cottid species, Porocottus leptosomus, is described on the basis of 12 specimens collected from Taean, west coast of Korea, Yellow Sea. The species is distinguished from other species of Porocottus by the following combination of characters: a strongly compressed body, two pairs of branched cirri on the dorsal surface of the head, bases of head cirri smooth, a single cirrus on the dorsal tip of each spine of the first dorsal fin, a single opening of the sixth canaliculus of the infraorbital sensory canal, a long posterior medial canaliculus of the occipital canal with the terminal pore and a few supplementary pores, and melanophores on the isthmus hidden beneath the branchiostegal membrane. Received: January 11, 2001 / Revised: February 7, 2002 / Accepted: March 4, 2002     

Ontogeny of the cranial musculature in Corydoras aeneus Callichthyidae,Siluriformes

A complete study of the early ontogeny of the cranial muscles of Corydoras aeneus (Callichthyidae) was undertaken and results were compared with those for the loricariid Ancistrus cf. triradiatus. This comparison reveals a high degree of similarity in the ontogeny of both species' cranial muscles. Both species lack a musculus protractor hyoidei, and the musculus intermandibularis posterior is divided into two different parts that have partly obtained a novel function (serving the lower lip) in A. cf. triradiatus. A similar increase in muscular complexity in this species is found in the dorsal constrictor of the hyoid muscle plate. This constrictor gives rise to the same muscles in both C. aeneus and A. cf. triradiatus, but in A. cf. triradiatus the musculus levator operculi later hypertrophies. In C. aeneus the musculus extensor tentaculi forms a single muscle diverging posteriorly, whereas in A. cf. triradiatus the musculus extensor tentaculi differentiates into two separate bundles. Also, a loricariid neoformation is present called the musculus levator tentaculi.     

The morphology and vasculature of the respiratory organs of terrestrial hermit crabs (Coenobita and Birgus): gills,branchiostegal lungs and abdominal lungs

The morphology and vasculature of the respiratory organs of the terrestrial coenobitids were studied using light microscopy, TEM, SEM and corrosion casting. The gills of Coenobita and Birgus are modified for air-breathing but are reduced in number and size and have a comparatively small surface area. The branchiostegal lungs of Coenobita (which live in gastropod shells) are very small but are well vascularized and have a thin blood/gas barrier. Coenobita has developed a third respiratory organ, the abdominal lung, that is formed from highly vascularized patches of very thin and intensely-folded dorsal integument. Oxygenated blood from this respiratory surface is returned to the pericardial sinus via the gills (in parallel to the branchiostegal circulation). Birgus, which does not inhabit a gastropod shell, has developed a highly complex branchiostegal lung that is expanded laterally and evaginated to increase surface area. The blood/gas diffusion distance is short and oxygenated blood is returned directly to the pericardium via pulmonary veins. We conclude that the presence of a protective mollusc shell in the terrestrial hermit crabs has favoured the evolution of an abdominal lung and in its absence a branchiostegal lung has been developed.     

Succinic dehydrogenase activity of the respiratory muscles of a fresh-water teleost, Bagarius bagarius (Ham.) (Sisoridae, Pisces).

Functional morphology including the origin, insertion, and innervation of the respiratory muscles in relation to buccal pressure pump and opercular suction pumps in a fresh-water bottom dwelling siluroid fish, Bagarius bagarius have been studied. Histochemical studies were made on the succinic dehydrogenase activity of adductor mandibulae, retractor tentaculi, levator operculi, dilatator operculi, adductor operculi, intermandibularis, interhyoideus, hyohyoideus superior and constrictor branchialis. The intensity of reaction reveals the presence of three types of muscle fibres in some of the respiratory muscles. The muscle containing red muscle fibres are mostly innervated by the branches of the VIIth cranial nerve. The retractor tentaculi consists of superficial white muscle fibres and the interior part is dominated by red muscle fibres. The muscles (adductor operculi, levator operculi, dilatator operculi, interhyoideus, hyohyoideus superior) concerned with the opercular suction pumps are of mixed type and consist of white and red muscle fibres, whereas adductor mandibulae and intermandibularis are made up entirely of white muscle fibres. The adductor muscle bundles of the constrictor branchialis, which are responsible for movement of gill filaments, are dominated by the red muscle fibres. The abductor part, however, is made up entirely of white muscle fibres.     

中国南海蛇鳗科一新纪录属及一新纪录种(鱼纲,鳗鲡目)

报道了中国南海蛇鳗科1新纪录属Echelus Rafinesque,1810和1新纪录种Echelus uropterus(Temminck et Schlegel,1846).该属的特征为:尾鳍、胸鳍存在;背鳍起点在胸鳍后端之前;头部无额骨孔、眶后孔和上颞骨孔;鳃孔中等大;鳃膜骨条连于舌骨或上舌骨尖前.该种的特征:尾尖柔软;颌齿和犁骨齿颗粒状,带形;后鼻孔在上唇边缘外侧.     

Anatomy and innervation of the abdominal segmental muscles in larval and adult Tenebrio molitor (Coleoptera)

The external morphology, musculature, and the innervation of the abdominal segments were examined in larvae and adult Tenebrio molitor. In the larva, there are 26 pairs of muscles arranged at four different levels in the ventral, lateral, and dorsal region of each segment. In the adult, the number of muscles has been dramatically reduced and is limited to six pairs of muscles located at the dorsal and lateral region of the segment. These muscles, in either larval or adult stages, are innervated by two main nerves, n1 and n2, which originate from the segmental ganglia. The cell bodies of the motoneurons innervating the muscles of the 3rd abdominal segment are located in the 3rd and 2nd abdominal ganglia. Some cell bodies are retained throughout metamorphosis, but others disappear during the larva-pupa transition.     

Anatomy of the extrinsic gut musculature of Gammarus minus (Crustacea: Amphipoda)

Inserting on the buccal and esophageal foregut of Gammarus minus are numerous pairs of serially arranged dorsal dilator muscles, a single pair of lateral muscles, and two pairs of posterior muscles. Muscles of the cardiac stomach include three dorsal sets, a single pair associated with the pterocardiac ossicles, and two pairs inserting on the ventral aspect. A single pair of muscles inserts on the lateral aspect of the pyloric stomach. The extrinsic muscles of the foregut originate from exoskeletal apodemes of the cephalothoracic cuticle, sockets of the mandible, and a maxillary bridge that lies just ventral to the cardiac stomach. The extrinsic musculature of the hindgut is restricted to the rectal region and consists of paired dorsal and ventral series in an X-configuration. A single unpaired muscle inserts on the ventral midline. Extrinsic muscles of the hindgut originate from the integument of the last pleonic segment. The general arrangement of extrinsic gut muscles in G. minus is similar but not identical to that of other amphipods studied. However, the pattern is quite different from that of other malacostracans.     

Pterocryptis buccata, a new species of catfish from western Thailand (Teleostei: Siluridae) with epigean and hypogean populations

Pterocryptis buccata sp. nov. is described from the vicinity of Sai Yok, Kanchanaburi Province, western Thailand. It can be distinguished from all other congeners by its prominent mandibular muscles causing the cheeks to appear inflated and the following unique combination of characters: 54–61 anal-fin rays, 7 pelvic-fin rays, 50–52 vertebrae, 4 mandibular barbels and vomerine teeth present in 2 separate patches. An achromatic population inhabits the Sai Yok Noi cave. This is the first report of a cavedwelling catfish from Southeast Asia.     

Development and changes at settlement in the barbel structure of the reef fish,Upeneus tragula (Mullidae)

Synopsis The development of the sensory barbels of the tropical goatfish, Upeneus tragula (Mullidae), was examined from their first appearance early in planktonic life through to the reef-associated juvenile period. The structure of the barbel was examined histologically and found to represent an outgrowth of the gustatory (taste) system, composed of at least 50% sensory tissue at settlement. Abrupt changes in morphology were found to be coincident with the 6–12 h settlement period: barbels rapidly moved forward along the hyoid arch to abut the dentary; the length of the barbels increased by up to 52%; the epidermal layer increased to comprise 75% of the cross-sectional area; and the mean size of the taste bud cells increased by up to 100%. A strong relationship was found between barbel length and mean taste-bud size. This relationship was used to predict the mean taste-bud sizes for 237 newly-settled fish, collected as 12 samples over two recruitment seasons. Mean taste-bud size varied significantly among samples. Experiments examined whether food availability or temperature of the water within the pelagic phase influenced the size of the barbels at settlement. Food availability influenced the relationship between barbel length and fish size. Slower growing fish had larger barbels relative to fish length than those that grew faster. Temperature did not influence the relationship between barbel length and fish size. Variability in sensory development at settlement, and the factors which influence it, may have important ramifications for the potential success of the fish once on the reef.     

Enormous gill chambers of deep-sea coffinfishes (Lophiiformes: Chaunacidae) support unique ventilatory specialisations such as breath holding and extreme inflation

Deep sea habitats tend to favor species with low energetic demands, and therefore we predict that deep sea fishes will have behavioral and morphological specializations of the gill ventilatory system to reduce the energetic cost of pumping water across the gills. However, it is difficult to study functional morphology of deep sea fishes due the lack of ability to conduct laboratory experiments with living fishes. For this study, we combined analysis of publicly available video recorded by remote-operated vehicles (ROV) with detailed anatomical study of museum specimens to document the functional morphology of the massive gill chambers that are observed in coffinfishes (Lophiiformes: Chaunacidae). Chaunacids, like other lophiiforms, exhibit highly specialised ventilatory anatomy such as an enlarged branchiostegal apparatus and restricted gill openings, but videos show them using this anatomy in a new and unusual way. We observed eight individuals ventilating extremely slowly at rates of 0.03–0.004 Hz, during which the gill chambers were full yet we saw no inhalation or exhalation for periods of 26 to 245 s. This holding breath behaviour has not been observed in any other fishes and is probably highly energetically efficient. This inflation of the gill chambers also increases body volume by up to 30%, making them more globose and difficult to be taken as prey, much like stomach inflation in pufferfishes (Tetraodontidae). We also used micro computed-tomography (CT) scans to document the enormous branchiostegal rays and associated muscles that support this unique behaviour.     

Extrinsic Snout Musculature in Afrotheria and Lipotyphla

As currently recognized, the mammalian order Lipotyphla contains six extant families: Chrysochloridae, Erinaceidae, Solenodontidae, Soricidae, Talpidae, and Tenrecidae. Although most mammalogists have accepted this taxon, the morphological support for Lipotyphla is relatively weak, and recent phylogenetic studies using molecular data have concluded that it is not monophyletic. Instead, these molecular studies place chrysochlorids and tenrecids in the proposed clade Afrotheria, together with aardvarks, elephants, elephant shrews, hyraxes, and sirenians. Despite strong molecular support, Afrotheria has received little or no morphological support. It was recently suggested that a mobile snout might be a morphological feature uniting afrotherians. To test this proposal, I dissected the extrinsic snout musculature in an assortment of lipotyphlan and afrotherian mammals. These muscles provide support for Lipotyphla but not for Afrotheria. The snout is moved by different muscles in different afrotherian taxa, suggesting that the mobile snout is not homologous across different afrotherian lineages. In contrast, lipotyphlans have a distinctive set of five snout muscles moving the snout tip that appears to be unique to these six families. In addition, in soricids and talpids, four of the five snout muscles originate posterior to the zygomatic arch, supporting sister-taxon status for these two lineages. Although the extrinsic snout musculature does not support Afrotheria as presently proposed, it is consistent with an Afrotheria that does not include chrysochlorids and tenrecids.     

Morphometry and microanatomy of the barbels of the common sawshark Pristiophorus cirratus (Pristiophoridae): implications for pristiophorid behaviour

The internal anatomy of the barbels of the common sawshark Pristiophorus cirratus was examined with light microscopy to clarify their sensory role. No sensory structures such as taste buds (chemoreception), ampullae of Lorenzini (electroreception) or free neuromasts (lateral line mechanoreception) could be located in the barbels. The presence of bundles of nerve fibres, however, indicates a tactile function for the barbels. Conveyance of information regarding potentially damaging stimuli (nociception) and temperature (thermoception) cannot be excluded at this stage. It is hypothesized that the barbels are used by P. cirratus to locate prey in both the water column and on the substratum via wake detection and sensing changes in surface texture. The barbels may also be involved in the detection of water currents for rheotaxis. Regression analyses on P. cirratus morphometric data showed that the width of the rostrum at two sections (the barbels and the rostrum tip) does not significantly correlate with total length. The regression analyses also suggested that the barbels of P. cirratus may be lateralised.