A new species of <Emphasis Type="Italic">Trichodina</Emphasis> Ehrenberg, 1830 (Ciliophora: Trichodinidae) infecting farmed <Emphasis Type="Italic">Clarias gariepinus</Emphasis> (Burchell) (Siluriformes: Clariidae) in Cuba

A new species of Trichodina Ehrenberg, 1830 collected from the skin and fins of farmed North African catfish Clarias gariepinus (Burchell) fingerlings, is described. The new species can be distinguished from other trichodinids by the characteristics of the adhesive disc, especially by the great number of denticles. Trichodina merciae n. sp. is morphologically similar to T. renicola (Mueller, 1931) and T. marplatensis Martorelli, Marcotegui & Alda, 2008, in the number of denticles, but differs in the morphometric data, denticle morphology, environment and location. Trichodina merciae n. sp. has broad sickle-shaped blades and thin, straight rays, while T. marplatensis has broad club-shaped blades and wide S-shaped rays. Besides, denticle length, blade length, ray length, width of central part and denticle span of the new species are greater than T. marplatensis. However, the diameter of denticle ring and the diameter of the central area in T. marplatensis is larger than the ones in T. merciae n. sp. This is the first record of freshwater ectoparasite trichodinid with an average number of denticles greater than 50.     

Anomalies in the expression of abdominal denticle belts of partial larvae produced by fragmentation of theDrosophila melanogaster egg

Summary Abnormal denticle belt patterns can occasionally be observed in abdominal belts of partial larvae obtained from egg fragments. The abdominal belts have the following features in common: 1) The number of denticles of an abdominal denticle belt may increase, depending on the space occupied by a distinct segment or the whole body region. The arrangement of the denticles in such enlarged belts is less regular than in normal belts. 2) Enlarged denticle belts are also found in the terminal segment of a fragment, or in the segment next to it when the larval pattern is interrupted by fragmentation. The denticle belt in the adjacent segment(s) may then be supressed. 3) All denticles in a belt (or part of a belt) are orientated posteriorly if the distance to the posteriorly adjacent belt (or part of a belt) is larger than normal, or if this denticle belt is suppressed. Conditions anterior to a segment do not seem to exert any influence on denticle orientation.     

Diversity of dermal denticle structure in sharks: Skin surface roughness and three‐dimensional morphology

Shark skin is covered with numerous placoid scales or dermal denticles. While previous research has used scanning electron microscopy and histology to demonstrate that denticles vary both around the body of a shark and among species, no previous study has quantified three‐dimensional (3D) denticle structure and surface roughness to provide a quantitative analysis of skin surface texture. We quantified differences in denticle shape and size on the skin of three individual smooth dogfish sharks (Mustelus canis) using micro‐CT scanning, gel‐based surface profilometry, and histology. On each smooth dogfish, we imaged between 8 and 20 distinct areas on the body and fins, and obtained further comparative skin surface data from leopard, Atlantic sharpnose, shortfin mako, spiny dogfish, gulper, angel, and white sharks. We generated 3D images of individual denticles and measured denticle volume, surface area, and crown angle from the micro‐CT scans. Surface profilometry was used to quantify metrology variables such as roughness, skew, kurtosis, and the height and spacing of surface features. These measurements confirmed that denticles on different body areas of smooth dogfish varied widely in size, shape, and spacing. Denticles near the snout are smooth, paver‐like, and large relative to denticles on the body. Body denticles on smooth dogfish generally have between one and three distinct ridges, a diamond‐like surface shape, and a dorsoventral gradient in spacing and roughness. Ridges were spaced on average 56 µm apart, and had a mean height of 6.5 µm, comparable to denticles from shortfin mako sharks, and with narrower spacing and lower heights than other species measured. We observed considerable variation in denticle structure among regions on the pectoral, dorsal, and caudal fins, including a leading‐to‐trailing edge gradient in roughness for each region. Surface roughness in smooth dogfish varied around the body from 3 to 42 microns.     

The denticle surface of thresher shark tails: Three-dimensional structure and comparison to other pelagic species

Shark skin denticles (scales) are diverse in morphology both among species and across the body of single individuals, although the function of this diversity is poorly understood. The extremely elongate and highly flexible tail of thresher sharks provides an opportunity to characterize gradients in denticle surface characteristics along the length of the tail and assess correlations between denticle morphology and tail kinematics. We measured denticle morphology on the caudal fin of three mature and two embryo common thresher sharks (Alopias vulpinus), and we compared thresher tail denticles to those of eleven other shark species. Using surface profilometry, we quantified 3D-denticle patterning and texture along the tail of threshers (27 regions in adults, and 16 regions in embryos). We report that tails of thresher embryos have a membrane that covers the denticles and reduces surface roughness. In mature thresher tails, surfaces have an average roughness of 5.6 μm which is smoother than some other pelagic shark species, but similar in roughness to blacktip, porbeagle, and bonnethead shark tails. There is no gradient down the tail in roughness for the middle or trailing edge regions and hence no correlation with kinematic amplitude or inferred magnitude of flow separation along the tail during locomotion. Along the length of the tail there is a leading-to-trailing-edge gradient with larger leading edge denticles that lack ridges (average roughness = 9.6 μm), and smaller trailing edge denticles with 5 ridges (average roughness = 5.7 μm). Thresher shark tails have many missing denticles visible as gaps in the surface, and we present evidence that these denticles are being replaced by new denticles that emerge from the skin below.     

A new species of Tricorythodes Ulmer (Ephemeroptera: Leptohyphidae) from Minas Gerais, Southeastern Brazil

Tricorythodes molinerii sp. n. is described and illustrated based on nymphs from southeastern Brazil. The new species can be distinguished from other species of Tricorythodes Ulmer by the following characters: 1) genal projection present; 2) maxillary palp bi-segmented, with short apical seta; 3) pronotum with well developed anterolateral projection; 4) dorsum of fore femora with a transverse row of setae; 5) tarsal claws without marginal denticles and with one submarginal denticle on each side; 6) operculate gills triangular, shaded with black, and with whitish mark in subbasal zone; and 7) very large size.     

江西崇义地区上泥盆统节甲类(Arthrodira)的新材料

我国泥盆系鱼化石非常丰富,尤其是下、中泥盆统。但是,上泥盆统鱼化石发现尚少,而且主要是胴甲类化石,节甲类化石则很少发现。潘江（１９６２）在对斯行健已记述的一植物化石 Ｃｈａｎｇｙａｎｏｐｈｙｔｏｎ ｈｏｐｅｉｅｎｓｉｓ Ｓｚｅ重新进行观察时认为,该化石应属于盾皮鱼类,并将其归人瓣甲类 Ｍａｃｒｏｐｔｅｔａｌｉｃｈｔｈｙｉｄａｅ（？）,化石仅包括前腹侧片和胸棘。 Ｄｅｎｉｓｏｎ（１９７８）根据潘江的文章和插图则认为, Ｃｈａｎｇｙａｎｏｐｈｙｔｏｎ ｈｕｐｅｉｅｎｓｉｓ属于原始节甲类或者瓣甲类。王念忠等…     

An Alpine immigrant: Phragmoceras Broderip, 1839 from the Silurian of the Carnic Alps (Austria)

A rare occurrence of Phragmoceras imbricatum Barrande is recorded from moderately shallow marine Silurian sequences in the Carnic Alps (Austria). The specimen was collected from a condensed series of nautiloid-bearing wackestones/packstones which are documented as being one of the earliest levels of the Silurian Cephalopod Limestone Biofacies deposited along the North Gondwana margin. The presence of this genus and particular species in the Alpine area, whether as an in situ fauna or as a “stray immigrant”, during a period of global eustatic lowstand, adds new data with regard to the mechanisms of faunal exchange of nectobenthic nautiloid taxa between the Carnic Alps, the Prague Basin, SW Sardinia, Avalonia and Baltica which must have been made possible by currents connecting all five areas. It seems likely that some of the nautiloid taxa appearing in the Prague Basin during the Ludlow may have already been present in the Carnic Alps much earlier in the Silurian; these document early faunal affinities with Baltica. As well as confirming the existence of open migrational seaways between these terranes at a precise stratigraphic interval during the Silurian (lower Homerian: Wenlock), the presence of this species also indicates a prevailing more temperate paleoenvironment in these areas which this element of a usually tropical fauna could tolerate, and provides significant evidence that warm water currents reached the Carnic Alps at this time. In addition due to the bathymetric restrictions of the shells of these particular faunas, exchange by currents could not have taken place over great distances, even considering drifted individuals, and therefore indicates the relatively close positions/connections of various peri-Gondwana Terranes such as the Carnic Alps, SW Sardinia and the Prague Basin to Avalonia and Baltica during this time slice.     

Gill raker structure and development in indo-pacific anchovies (Teleostei: Engrauloidea), with a discussion of the structural evolution of engrauloid gill rakers

The postlarval development of gill raker denticles is described for the engrauloid (anchovy) genera Coilia, Lycothrissa, Setipinna, Thryssa, Stolephorus, and Encrasicholina based on scanning electron microscopy. The raker structure of adult Papuengraulis is also described. In the coiliid genera Coilia, Lycothrissa, Setipinna, Thryssa, and Papuengraulis, denticle development is not confined to particular region(s) of the raker. With few exceptions, the proliferation of denticles with growth is greatest along the upper raker edge; denticles are smaller and less dense on the raker faces and along the lower raker edge. Some Thryssa and Setipinna have a derived condition of denticle clustering along the upper raker edge. In Stolephorus and Encrasicholina, denticle development is confined to the upper raker half and includes the development of a single row of denticles along each raker face. A phylogenetic analysis of engrauloid raker structure, incorporating data from Bornbusch ( 88: Copeia 1988:174–182) and based on outgroup comparisons, indicates that for the Engrauloidea: (1) the pattern of denticle development shared by coiliids is plesiomorphic; and (2) the pattern of denticle development shared by Stolephorus, Encrasicholina, and most other engraulids is synapomorphic for the Engraulidae. There is no evidence that the studied coiliids Stolephorus and Encrasicholina are suspension feeders. The engraulid pattern of raker denticle development which is retained in suspension feeding engraulids of the genus Engraulis was thus derived before the derivation of suspension feeding in Engraulis. Comparative morphological and phylogenetic studies of clupeomorph raker structures and feeding behaviors can infer the historical origins of morphology-behavior associations, help define possible directions for analyses of raker denticle function, and thereby help elucidate the significance of structure-function couplings in the evolution of such clupeomorph trophic behaviors as suspension feeding. © 1992 Wiley-Liss, Inc.     

Aquatic nematodes from Ethiopia V

Three species of chromadorids two of which are new to science are described from bottom samples of Lake Tana, L. Ziway and River Abbay, Ethiopia. Achromadora inflata n. sp. and Ethmolaimus zullinii n. sp. are characterized by a uniquely inflated and offset anterior end. The latter is an exception in its genus also by its possession of a well developed dorsal tooth and inconspicuous ventrosublateral denticles. Prodesmodora nurta Zullini, 1988 is reported here for the first time out of its type locality and is described in detail. SEM pictures of Ethmolaimus zullinii n. sp. and Prodesmodora nurta, and complete setae maps of the three species are also presented.Abbreviations used ABE = anterior body end - ABW = anal body width - Amph = amphid - Amph W = amphidial fovea width - CBW = corresponding body width - CSL = cephalic setae length - Ddent = dorsal denticle - GL = gonad length - L = length - LM = light microscope - LRW = lip region width - MBW = maximum body width - n = number of specimens - NR = nerve ring from the anterior end - PBE = posterior body end - Ph L = pharyngeal length (neck length) - PrL = prerectal length - RL = rectal length - SEM = scanning electron microscope - V-A = distance from vulva to anus - Vdent = ventral denticle - W = width     

Scanning electron microscopy of the lip denticiles of Ascaris suum adults of known ages.

Purebred Hampshire pigs, farrowed and maintained under conditions precluding extraneous helminth infection, were exposed to a single dose of 10,000 Ascaris suum infective eggs. The pigs were killed at intervals of 28, 41, 55, 86, 115, 145, 175, and 206 days after infection. At necropsy, no gross lesions were found in the lungs or livers of infected pigs. The worms were recovered from the small intestine, identified, counted, and fixed. The heads were excised, critical point dried, mounted en face, and examined by scanning electron microscopy. Worms 28 to 115 days old had unworn denticles that were triangular when viewed laterally but blunt when viewed tangentially. Wearing of the denticles was observed first with 145-day-old worms; wearing increased with age both in numbers of denticles affected and in degree of wear so that by 206 days after inoculation, almost all denticles in the center of the lip were worn. Worn denticles appear truncated when viewed from any angle. The denticles outside the central area were not affected by wear. The size of the denticles varies not only between specimens of the same age, but also on each specimen. However, average denticle size is directly related to the size and, accordingly, to the age of the worm. External to each denticle is a corresponding depression that we have called the denticular groove. One 28-day-old specimen had some extra denticles aligned irregularly along the lip; this irregularity gave the appearance of a double row. The denticles of the two subventral lips are similar to those of the dorsal and are equally affected by wear. There was no detectable difference in denticles of male and female worms. Since wear can now be specifically correlated with age, we conclude that the denticles are functional and become worn through use. Consequently, adult A. suum may be an even more injurious pathogen than heretofore supposed.     

The fin spine of a new holocephalan from the lower jurassic of Lyme Regis,Dorset, England

A fin spine previously described as ‘Myriacanthus paradoxus’ Agassiz from the Lower Lias (Lower Jurassic) of Lyme Regis, is allocated to the new genus and species Recurvacanthus uniserialis. The spine is unusual in possessing a single median row of four large, hook-like, downturned denticles on the distal part of the posterior wall. It is concluded that the unique specimen should be classified with the myriacanthoid chimaeriform holocephalans since it possesses a tubercular ornament on the lateral walls.     

Placoderm fishes,pharyngeal denticles,and the vertebrate dentition

The correlation of the origin of teeth with jaws in vertebrate history has recently been challenged with an alternative to the canonical view of teeth deriving from separate skin denticles. This alternative proposes that organized denticle whorls on the pharyngeal (gill) arches in the fossil jawless fish Loganellia are precursors to tooth families developing from a dental lamina along the jaw, such as those occurring in sharks, acanthodians, and bony fishes. This not only indicates that homologs of tooth families were present, but also illustrates that they possessed the relevant developmental controls, prior to the evolution of jaws. However, in the Placodermi, a phylogenetically basal group of jawed fishes, the state of pharyngeal denticles is poorly known, tooth whorls are absent, and the presence of teeth homologous to those in extant jawed fishes (Chondrichthyes + Osteichthyes) is controversial. Thus, placoderms would seem to provide little evidence for the early evolution of dentitions, or of denticle whorls, or tooth families, at the base of the clade of jawed fishes. However, organized denticles do occur at the rear of the placoderm gill chamber, but are associated with the postbranchial lamina of the anterior trunkshield, assumed to be part of the dermal cover. Significantly, these denticles have a different organization and morphology relative to the external dermal trunkshield tubercles. We propose that they represent a denticulate part of the visceral skeleton, under the influence of pharyngeal patterning controls comparable to those for pharyngeal denticles in other jawed vertebrates and Loganellia.     

Morphology of the oral disc of Bufo bufo (Salientia: Bufonidae) tadpoles

The fully developed oral disc of the tadpole of Bufo bufo consists of dorsal and ventral labia bearing, respectively, two and three ridges bearing numerous horny denticles, a horny beak provided with jaw sheath serrations, and large lateral papillae that are borne by two cutaneous plicae. As development progresses toward metamorphosis, these structures gradually regress until they disappear. Each cusped clavate labial denticle adheres, by means of a thin peduncle, to a similar labial denticle fixed in the lip and formed by a group of three or four cells that keratinize gradually and thus present remarkable differences in their morphology. Once all the cells of a group have been converted into horny tissue, the denticle sheds and is replaced by the underlying one. The beak serrations also are horny structures; each consists of a columnar band of cells which undergoes a gradual keratinization. The horny cells that detach themselves at intervals, being replaced by those of the underlying anlagen. The labial denticles and the beak serrations keratinize in two distinct ways. In the former, the desmosomal filaments appear to play an important role whereas, in the latter, the keratin seems to be synthesized “ex novo” by the ribosomes.     

<Emphasis Type="Italic">Angiostoma namekuji</Emphasis> n. sp. (Nematoda: Angiostomatidae) from terrestrial slugs on Oshiba Island in the Seto Inland Sea,Japan

A new species of nematode, Angiostoma namekuji n. sp. (Angiostomatidae: Rhabditida), is described from the intestinal lumen of the terrestrial slug Philomycidae gen. sp. collected from Oshiba Island in the Seto Inland Sea, Hiroshima Prefecture, Japan. The new species is recognized by the following characteristics: body length 2,782–3,599 (mean 3,240) μm (male); 4,666–5,532 (5,030) μm (female); lateral field present; pharyngeal corpus with valves in the bulb; male with short tail, c = 35–57 (48), with one denticle; and seven pairs of genital papillae arranged as 1+2/3+1; female with tail having small denticles on distal tip; uterus c.50% of the body size; each ovary long, starting near vulva, not coiled, reflexed and reaching uterus; ovaries not crossing each other. Our phylogenetic tree based on sequences of the nuclear 28S ribosomal RNA gene supported the generic allocation of the new species in Angiostoma Dujardin, 1845.     

Three new species of Tricorythopsis (Ephemeroptera: Leptohyphidae) from southeastern Brazil

Three new species of Tricorythopsis Traver (Ephemeroptera: Leptohyphidae) are described and illustrated based on nymphs from southeastern Brazil. These new species can be distinguished from other species of the genus by the following characters: Tricorythopsis araponga sp. n.: (1) femora with long setae; (2) abdominal segments 5–7 with dorsal tubercles; (3) tarsal claws with 4–6 marginal denticles and 7 + 4 submarginal denticles. Tricorythopsis baptistai sp. n.: (1) tarsal claws with 4–5 large marginal denticles and one submarginal denticle on each side; (2) abdominal colour pattern; (3) abdomen without tubercles; (4) coxae without projections. Tricorythopsis pseudogibbus sp. n.: (1) abdominal segments 6–8 with small dorsal tubercles; (2) tarsal claws with four large marginal denticles, and 3 + 1 or 2 submarginal denticles; (3) coxae dorsally projected; (4) femora broad and with short setae; (5) pronotum with anterolateral projection.     

Permian bryozoans of the NW-tethys

Summary Permian bryozoan faunas from the Lower Permian sequences of the Carnic Alps (UpperPseudoschwagerina Formation and Trogkofel Formation) and from some other Permian units of the NW-Tethys (Sicily, Tunisia) include cystoporid, trepostomid, fenestellid, rhabdomesid, and timanodictyid taxa. Fenestellids and cystoporids species dominate. The Lower Permian bryozoan fauna of the Carnic Alps displays close relations to faunas of Sakmarian-Artinskian age of the Russian Platform and Pamir as well as of the Lower Permian of Australia. Bryozoans from Permian sequences of Sicily and Tunisia display relations to the Permian faunas of Indonesia and Australia.     

A New Lanternshark <Emphasis Type="Italic">Etmopterus splendidus</Emphasis> from the East China Sea and Java Sea

A new species of the lanternshark Etmopterus splendidus is described. This new species is distinguished from the congeners by the combination of the following characters: distance from snout tip to 1st dorsal spine much less than distance from the spine to upper caudal origin; caudal fin short, much less than head length; dermal denticles on lateral side of trunk with very small, erect thornlike, conical crowns, those on trunk arranged in regular longitudinal rows, and distinctly arranged on interdorsal area and on lateral trunk of interspace between 2nd dorsal and caudal, but not arranged in regular longitudinal rows on dorsal surface of interorbital and o abdomen; color in life purplish-black above and with inconspicuous bluish-black flank marks and three other bluish-black marks at base of caudal fin and along its axis; shape of flank marks narrow anterior to, but broader posterior to pelvic fins.     

An SEM study of adhesive disc skeletal structures isolated from trichodinids (Ciliophora: Peritrichida) of the genera Trichodina Ehrenberg, 1838 and Paratrichodina Lom, 1963

Specimens of Trichodina domerguei Wallengren, 1897, T. intermedia (Lom, 1961) and Paratrichodina incissa (Lom, 1959) were sonicated to liberate skeletal components of the adhesive disc. This enabled SEM observation of the taxonomically important structures obscured in preparations of complete cells. A previously undescribed peg-like structure on the centrifugal surface of the central part of the denticles is revealed in T. domerguei. In P. incissa the ray apophysis and its supporting apophysis appear to be absent, providing an additional characteristic to discriminate it from species of the genus Trichodina Ehrenberg, 1838. From silver stained and SEM preparations of T. intermedia and P. incissa important differences in denticle blade form are apparent, underlining the value of observation of isolated skeletal structures by electron microscopy.     

Morphogenese und Musterbildung des Hautzähnchen-Skelettes von Heterodontus

Different denticle shapes in Heterodontus (Selachii) are derived from a single primary form by five geometrical transformations. Insertion of new denticles into the existing pattern is controlled by reference points transmitting positional information which is space- and time-dependent. Injuries interrupt the transmission of certain informations, causing anomalous denticles, which do not occur in normal ontogeny.
Dic verschiedenen Zähnchenformen lassen sich von einer einzigen Grundform durch fünf verschiedene geometrische Transformationen ablciten. Das Einfügen neuer Zähnchen in das existicrende Muster wird durch Referenzpunkte kontrolliert, die Lage- und Zeit-abhängige lnfoimationen übertragen. Verwundungen unterbrechcn die Übermittlung be-stimmter Informationen. Dies führt zu anomalen Zähnchen, die in der normalen Onto-gencsc nicht vorkommen.     

Two trichodinid ectoparasites from marine molluscs in the Yellow Sea,off China,with the description of <Emphasis Type="Italic">Trichodina caecellae</Emphasis> n. sp. (Protozoa: Ciliophora: Peritrichia)

The morphology and infraciliature of two ectoparasitic ciliates, Trichodina caecellae n. sp. and T. ruditapicis Xu, Song & Warren, 2000, parasitising the gills of marine molluscs from the Shandong coast of the Yellow Sea, China, were investigated following wet silver nitrate and protargol impregnation. T. caecellae was found on the small marine sand clam Caecella chinensis Deshayes and is distinguished mainly by the acute triangle-like blade, the very delicate central part and the needle-shaped ray. T. ruditapicis was studied based on four populations from three clams: two populations from Ruditapes philippinarum (Adams) and one each from Saxidomus purpuratus (Sowerby) and Solen grandis Dunker. All four populations fell within the range of morphometry and agreed closely in the overall appearance of the adhesive disc. However, variability was found in the denticle structure, especially in populations from different host clams. Our observations suggest that denticle morphology may be more or less variable between and within populations, and that such minor differences should not be overestimated. It should be emphasised that, except for the denticle morphology, the bright granules or circles in the centre of the adhesive disc represent another important feature facilitating the identification of this trichodinid species.