Living in fast‐flowing water: Morphology of the gastromyzophorous tadpole of the bufonid Rhinella quechua (R. veraguensis group)

We describe the bufonid gastromyzophorous tadpoles of Rhinella quechua from montane forest streams in Bolivia. Specimens were cleared and stained, and the external morphology, buccopharyngeal structures, and the musculoskeletal system were studied. These tadpoles show a combination of some traits common in Rhinella larvae (e.g., emarginate oral disc with large ventral gap in the marginal papillae, labial tooth row formula 2/3, prenarial ridge, two infralabial papillae, quadratoorbital commissure present, larval otic process absent, mm. mandibulolabialis superior, interhyoideus posterior, and diaphragmatopraecordialis absent, m. subarcualis rectus I composed of three slips), some traits apparently exclusive for the described species of the R. veraguensis group (e.g., second anterior labial tooth row complete, lingual papillae absent, adrostral cartilages present), and some traits that are shared with other gastromyzophorous tadpoles (e.g., enlarged oral disc, short and wide articular process of the palatoquadrate, several muscles inserting on the abdominal sucker). In the context of the substantial taxonomic and nomenclatural changes that the former genus Bufo has undergone, and despite the conspicuous morphological differences related to the presence of an abdominal sucker, the larval morphology of R. quechua supports including it in the genus Rhinella and placing it close to species of the R. veraguensis assemblage. J. Morphol., 2009. © 2009 Wiley‐Liss, Inc.     

Internal and external morphology of the deutonymph of Caloglyphus boharti (Arachnida: Acari)

A band of flexible cuticle encircles the deutonymph, separating the dorsal and ventral plates. The coxae are large, flat and fused with one another to form most of the ventor. Individual coxal margins are redefined as sternites, epimerites or simply apodemes according to which margins fuse with which others. A given area of cuticle may have patches of dark or light cuticle not corresponding to particular structures or cuticular contours; this is a source of confusion to taxonomists. Each leg has a dicondylic coxal-trochantal (adduction-abduction) and trochantal-femoral (promotion-remotion) joint with opposing muscles. The three more distal monocondylic joints (flexion-extension) have only flexor muscles; extension is by increased haemolymph pressure. The five apodemes of the sucker plate provide rigidity; the four suckers attach by a flexible cuticular ring to a solid flange or socket in the sucker plate. The sucker muscles attach to the center of each sucker. The flat, external face of the sucker plate apodemes may complement sucker action by adhesion. Coxal discs and sucker plate discs are identical, contain birefringent cuticular elements, and are considered modified setae. Functional mouthparts and a pharynx are lacking, but a cheliceral anlage is present. The esophagus, midgut and caecae, and malpighian tubules are lumenless and the cells small. The hindgut has a lumen, larger cells and opens externally via the anus. Whereas the digestive tract is regressed, the reproductive system is yet incompletely developed. In older deutonymphs anlagen of ducts, accessory glands and gonads are discernible. The nature of the haemocoel and peritoneum remains nuclear. The central nerve mass is conspicuously large for the size of the deutonymph. The supraesophageal ganglion gives rise to the cheliceral nerves; all other nerves arise from the subesophageal ganglion. Most major nerves were traced to the effector organs. The muscles are divided into leg, dorso-ventral (derived from coxal muscles), dorsal, sucker, and anogenital muscles. The trochantal adductor muscles originate on an endosternite, which is supported by muscles running to the dorsal hysterosoma. The dorso-ventral and propodosomal retractor muscles affect haemolymph pressure. The massive sucker retractor muscles are unique to this instar. Anogenital muscles are not well developed.     

The organization of the muscle system of the causative agent of dicrocoeliosis,Dicrocoelium dendriticum

The musculature of parasitic flatworms plays a central role in locomotory movement, attachment to the host, and in the function of the digestive, reproductive, and excretory systems. We examine for the first time the muscle system of the flatworm Dicrocoelium dendriticum, a causative agent of the parasitic disease dicrocoeliosis, by use of fluorescently labeled phalloidin and confocal laser scanning microscopy. Somatic musculature of D. dendriticum consists of the circular, longitudinal, and diagonal muscles. The distribution of the muscle fibers in the body wall differed among the anterior, middle, and posterior body regions of the worm. The musculature of the attachment organs, the oral and ventral suckers, includes several types of muscles: the external equatorial and meridional muscles, internal circular and semicircular muscles, and radial muscles. Inside of the ventral sucker the diagonally located muscles were revealed and the supplementary u-shaped muscles were found adjoined to the base of the sucker from outside. The musculature of the internal organs composed of the excretory, reproductive, and digestive systems were characterized. Our results increase our knowledge of the morphology of trematodes and the arrangement of their muscle system.     

Segregation by species and size classes of rainbow trout,Salmo gairdneri,and Sacramento sucker,Catostomus occidentalis,in three California streams

Synopsis The hypothesis that Sacramento suckers, Catostomus occidentalis, compete with rainbow trout, Salmo gairdneri, for space in streams was examined by measuring microhabitat utilization of both species in three California streams. Two streams were similar in most respects except one contained only trout and one contained trout and a large population of suckers. The third stream, formed by the union of the first two, contained trout and a small population of suckers. The species overlapped in five of the six microhabitat variables measured: maximum depth, mean water column velocity, focal point velocity, surface water velocity, and substrate type. However, the species had strong vertical segregation; there was little overlap between species in focal point depth. Mean focal point velocities were also significantly different. Suckers roamed over and generally remained in contact with the bottom while trout held position in the water column. Microhabitat utilization by trout in the stream without suckers was similar to in the stream with a higher sucker density. Differences in microhabitat utilization by trout between the third stream and the other two was attributed to the larger size of the third stream. Both sucker and trout showed a similar within-species segregation of size classes - fish under 50 mm in length sought shallow water. Size-specific trends indicated ontogenic shifts in resource utilization which reduced overlap within species. These results suggest that competition for space between trout and suckers was not a major factor regulating microhabitat utilization of trout, although the possibility that larger suckers may displace small trout needs further study.     

Resource subsidies from adfluvial fishes increase stream productivity

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Dactylosternum abdominale (F.) (Coleoptera: Hydrophilidae): A predator of the banana weevil

The efficacy of predators of the banana weevil was investigated under laboratory and field cage conditions for the different breeding sites of the pest viz. the growing banana sucker and the spent pseudostem and residual rhizome of the sucker after the harvest of the bunch. The indigenous Dactylosternum abdominale (Hydrophilidae) reduced weevil multiplication in suckers by up to 50% and in residual stumps of harvested suckers by 39%. In spent pseudostems D. abdominale reduced the multiplication by 40–90% at different predator population densities while Thyreocephalus interocularis (Staphylinidae) reduced it by 42%. Other predators were unimportant.     

Microsatellite markers for the endangered razorback sucker, Xyrauchen texanus, are widely applicable to genetic studies of other catostomine fishes

We developed 10 polymorphic microsatellite markers for the federally endangered razorback sucker, Xyrauchen texanus. PCR optimization and cross-species amplification experiments indicated that these markers will be useful for analysis of fine-scale population structure in razorback and two other sucker species; the white sucker, Catostomus commersonii and the Rio Grande sucker, C. plebeius. Alleles at locus Xte4 did not overlap when compared between razorback and bluehead (C. discobolus) suckers and permits detection of F1 hybrids. These microsatellite markers appear widely applicable for identifying genetic consequences of population decline, hatchery rearing and release, and hybridization in razorback and other castostomine suckers.     

The function of the suckers of larval net-winged midges (Diptera: Blephariceridae)

1. Larval net-winged midges (Diptera: Blephariceridae) possess six ventral suckers that enable them to inhabit swift streams. Each sucker consists of a suction disc and a cavity with a piston. Large muscles are inserted within the piston, as well as at the base of the suction disc. This structure infers that both attachment and release of the sucker is achieved by vertical movements of the piston.
2. Live observations of blepharicerid larvae revealed that the sucker is indeed attached by an upward movement of the piston, but that the cavity is flooded when the sucker is released. The piston is lowered only at the end of a sucker 'step', expelling water from the cavity.
3. During foraging, the maxilla and the piston of the first sucker are moved synchronously, indicating that the first sucker functions as a holdfast thus facilitating grazing.
4. The adhesive forces, as well as the relative size of blepharicerid suckers, differ amongst species. They are highest in Hapalothrix lugubris and lowest in Liponeura cordata , which correlates with the hydraulic stress to which the larvae of these species are exposed in their preferred habitat. The balance between the efficiency of their retention structure and the hydraulic conditions of their preferred habitat defines a key dimension of their ecological niche.     

Morphological and genetic structuring in the Utah Lake sucker complex

Population decline in the federally endangered June sucker (Chasmistes liorus), a lakesucker unique to Utah Lake, Utah, has been attributed in part to hybridization with the more widespread Utah sucker (Catostomus ardens). As a group, suckers in Utah Lake exhibit considerable external morphological variation. Meristic and morphological ambiguities, presumably the result of hybridization, create a continuum of intermediate forms between Chasmistes and Catostomus extremes and prevent definitive identification to species. Here we describe and evaluate the morphological and genetic variation in suckers in Utah Lake by comparing a morphological analysis with amplified fragment length polymorphism and microsatellite analyses. Suckers were morphologically differentiated using mouth characters associated with different feeding strategies: planktivory (June sucker) and benthivory (Utah sucker). Although we found no genetic evidence for a deep divergence between June and Utah morphs, significant, but slight population structuring accompanied the substantial morphological variation. Bayesian model‐based genetic clustering analyses detected two sucker populations in Utah Lake; however, these clusters were not strongly concordant with morphological groupings or between marker systems. The suckers in Utah Lake present an interesting dilemma regarding conservation: should one conserve (breed and stock) a subset of the morphotypic variation in the Utah Lake sucker complex, focusing on the endangered June sucker morphotype, or should one conserve both June sucker and Utah sucker morphotypes in this complex, possibly maximizing evolutionary potential? We explore this question in the context of current genetic and morphological variation in the Utah Lake sucker complex as well as historical information on this complex and other lakesuckers.     

Surface ultrastructure of the plagiorchid trematode Glossidium pedatum Looss, 1899 from bagrid fish in Egypt

The present study concerned the morphology and surface ultrastructure of a plagiorchid, Glossidium pedatum, from bagrid fish of the river Nile in Egypt. Adult G. pedatum have an elongate body, tapered towards the anterior and posterior ends. Their oral sucker is small, sub‐terminal and rounded, measuring 0.200 mm in diameter. Sensory papillae around the oral sucker usually occur in small clusters of three to eight each. The ventral sucker is large, situated at the anterior end of the second third of the body, 0.299 mm in diameter, and is surrounded by three pairs of sensory papillae. Both suckers have rounded rims covered by tegumental spines. On the anterior part of the ventral surface of the body tegumental spines are small, pointed and closely spaced. A small triangular area of tegument anterior to the ventral sucker is devoid of spines. Tegumental spines on the mid‐region of the body slightly increase in size and number, especially towards the lateral aspects and posterior to the ventral sucker. Towards the posterior end of the body the spines progressively decrease in both size and number. The dorsal side exhibits similar surface features but the spines are less numerous and slightly smaller.     

Development of the olfactory system of the white sucker,Catostomus commersoni,in relation to imprinting and homing: a comparison to the salmonid model

Synopsis White suckers,Catastomus commersoni, use olfactory cues to return to the same spawning stream year after year. If we assume that they follow a model similar to the well-known salmon model, olfactory imprinting must occur very early in their development. We describe the time of migration from the nursery stream in relation to the development of the white sucker olfactory system to determine if the requisite anatomical structures are present which would permit imprinting. At hatching the olfactory placode is present and beginning to differentiate, the lumen of the olfactory capsule is starting to form, and the olfactory tract projects into the telencephalon. Larvae migrate approximately 2 weeks later or at a size of 14 mm TL. At this time olfactory cilia are present, the olfactory tract is robust and the telencephalon is beginning to differentiate. Therefore, it appears that the fundamental neural structures necessary for imprinting are present. A comparison with salmon, however, clearly demonstrates that the white sucker olfactory apparatus is not as well developed as that of salmon at time of migration. This raises the question of the ability of white suckers to imprint in the same manner as salmon and whether the salmonid model is applicable to white suckers. Alternative imprinting hypotheses are discussed.     

Variation of apomorphic characters in stream-dwelling tadpoles of the bufonid genus Ansonia (Amphibia: Anura)

Six larval forms of the bufonid genus Ansonia from Borneo share the following synapomorphies: cup-like, ventral oral disc; an expanded post-dental portion of the lower lip, which has a papillate margin; upper keratinized jaw sheath divided; body markedly flattened ventrally; eyes set relatively far back on the body. All of these tadpoles live on the bottom in strong currents, except for larval Ansonia leptopus , which lives in drifts of dead leaves that accumulate in eddies within streams. These larval forms differ among themselves in body shape, development of inframarginal papillae on the lower lip, size of the gap between the keratinized parts of the upper jaw sheath, width of the post-dental portion of the lower lip, relative lengths of upper and lower rows of labial teeth, and arrangement of the gut coils. One form has an abdominal sucker. Changes in these characters are not correlated; the derived condition in one character is not always associated with the derived state in another. Consequently, these tadpoles cannot be arranged in a simple morphocline from least to most derived, again with the exception of A. leptopus , which is the least modified in all respects. Although tadpoles of Ansonia resemble those of the neotropical bufonid genus Atelopus in general specialization for benthic life in flowing water, they differ from that group in body form and details of the oral disc.     

A survey of shape variation in keratinized labial teeth of anuran larvae as related to phylogeny and ecology

Labial teeth of anuran tadpoles are keratinized structures derived from the activity of a single epidermal cell of the oral labia; they are not homologous with adult anuran teeth, nor with teeth of other vertebrates. The present study comprises a first approach for studying labial tooth shape variation that will be useful for future studies of comparative development and the functional mechanics of feeding structures. We examined interspecific shape variations in the labial teeth of anuran tadpoles and searched for correlations of these variations with ecomorphological guilds and phylogeny. Species ordination shows that important variations at various taxonomic levels are related mainly to the general curvature of the tooth axis, the angle between the labial tooth base and tip, head length and curvature, and sheath width. The teeth of most basal taxa are broad‐based and curved, although some broad‐based teeth also characterize some phthanobatrachian species. Teeth of hyloids and ranoids differ in the oral angle, overall curvature, and sheath width. A phylogenetically independent ecomorphological effect is significant only for lotic suctorial and gastromyzophorous guilds; teeth in these forms have short, thick and curved heads, wide sheaths, and generally acute oral angles. The lack of a significant correlation between labial tooth shape and trophic guilds suggests that labial tooth harvesting ability has a wide latitude that could be particularly functional only under specific circumstances. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 101 , 609–625.     

The structure and adhesive mechanism of octopus suckers

Octopus suckers consist of a tightly packed three-dimensionalarray of muscle with three major muscle fiber orientations:1) radial muscles that traverse the wall; 2) circular musclesarranged circumferentially around the sucker; and 3) meridionalmuscles oriented perpendicular to the circular and radial muscles.The sucker also includes inner and outer fibrous connectivetissue layers and an array of crossed connective tissue fibersembedded in the musculature. Adhesion results from reducingthe pressure inside the sucker cavity. This can be achievedby the three-dimensional array of muscle functioning as a muscular-hydrostat.Contraction of the radial muscles thins the wall, thereby increasingthe enclosed volume of the sucker. If the sucker is sealed toa surface the cohesiveness of water resists this expansion.Thus, the pressure of the enclosed water decreases instead.The meridional and circular muscles antagonize the radial muscles.The crossed connective tissue fibers may store elastic energy,providing an economical mechanism for maintaining attachmentfor extended periods. Measurements using miniature flush-mountedpressure transducers show that suckers can generate hydrostaticpressures below 0 kPa on wettable surfaces but cannot do soon non-wettable surfaces. Thus, cavitation, the failure of waterin tension, may limit the attachment force of suckers. As depthincreases, however, cavitation will cease to be limiting becauseambient pressure increases with depth while the cavitation thresholdis unchanged. Structural differences between suckers will thendetermine the attachment force.     

Root suckering patterns in Populus euphratica (Euphrates poplar, Salicaceae)

To understand the spatial structure of monospecific Tugai forests (Xinjiang Province, China) growing as gallery woods nourished by ground water, root suckering in Populus euphratica was studied by a combination of morphological and molecular analyses. Seedlings grow a deep tap root and keep this as adult trees, whereas root suckers never develop a tap root but utilize the horizontally stretching root of their parent trees. The resulting reverse “T” root architecture distinguishes reliably even adult root suckers from generatively grown trees. Due to assimilate input from the root sucker, the distal root (pointing away from the parent tree) becomes thicker soon than its proximal root, which allows determination of the direction of vegetative growth. One stand including 279 young trees germinated from seeds and 267 root suckers was mapped completely, and selected suckers were assigned to parent trees by genotyping with microsatellite DNA. Root suckers develop up to 40 m away from parent trees on horizontal “spacer” roots, usually originating not deeper than 20 cm below surface. Trees begin with root suckering between 10 and 15 years, shortly before reaching flowering age. Cutting experiments indicated reduced survival of young root suckers disconnected from the parent tree. Without a tap root and with a rooting point close to the surface, declining ground water levels should lower the fitness of root suckers even more than that of generatively grown trees.     

Effects of ambient Lake Mohave temperatures on development,oxygen consumption,and hatching success of the razorback sucker

Synopsis Spawning of razorback suckers,Xyrauchen texanus, in Lake Mohave occurred from 10–22°C and larvae were collected at water temperatures from 10–15°C in 1982 and 1983. In the laboratory, hatching success was similar from 12–20°C, but reduced hatching success was found at 10°C while none hatched a 8°C. Development rate and oxygen consumption were positively related to incubation temperature. Direct effects of ambient Lake Mohave water temperatures on hatching success of razorback sucker embryos are considered minimal. Historical spawning temperatures for the species are hypothesized based upon successful incubation temperatures and comparison to the white sucker,Catostomus commersoni.     

Habitat use and population characteristics of potentially spawning shovelnose sturgeon Scaphirhynchus platorynchus (Rafinesque, 1820), blue sucker (Cycleptus elongatus (Lesueur, 1817), and associated species in the lower Wisconsin River, USA

The goal of this study was to compare the possible locations, timing, and characteristics of potentially spawning shovelnose sturgeon (Scaphirhynchus platorynchus), blue sucker (Cycleptus elongatus), and associated species during the spring of 2007–2015 in the 149‐km‐long lower Wisconsin River, Wisconsin, USA, a large, shallow, sand‐dominated Mississippi River tributary. A 5‐km index station of two pairs of rocky shoals surrounded by sandy areas was electrofished for shovelnose sturgeon and blue sucker in a standardized fashion a total of 40 times from late March through mid‐June, the presumed spawning period. On one date in 2008 and two dates in 2012, all rocky shoals and adjacent sandy areas in the lowermost 149 km of the river were also electrofished for both species. Shovelnose sturgeon and blue sucker appeared to spawn in the limited rocky areas of the river along with at least four other species: mooneye (Hiodon tergisus), quillback (Carpiodes cyprinus), smallmouth buffalo (Ictiobus bubalus), and shorthead redhorse (Moxostoma macrolepidotum), usually at depths of 0.8–2.0 m and surface velocities of 0.4–1.0 m/s. However, apparently spawning shovelnose sturgeon were found only on mid‐channel cobble and coarse gravel shoals within a single 7‐km segment that included the 5‐km index station, whereas apparently spawning blue suckers were encountered on these same shoals but also more widely throughout the river on eroding bluff shorelines of bedrock and boulder and on artificial boulder wing dams and shoreline rip‐rap. Both species showed evidence of homing to the same mid‐channel shoal complexes across years. Blue sucker tended to concentrate on the shoals earlier in the spring than shovelnose sturgeon, usually from late April through mid‐May at water temperatures of 8.0–15.5°C along with quillback and shorthead redhorse. In comparison, shovelnose sturgeon usually concentrated on the shoals from mid‐May through early June at 13.5–21.8°C along with mooneye and smallmouth buffalo. Based on recaptures of tagged fish, at least some shovelnose sturgeon and blue sucker returned to the shoals at one‐year intervals, although there was evidence that female blue sucker may have been more likely to return at two‐year intervals. Most shovelnose sturgeon could not be reliably sexed based on external characteristics. Spawning shovelnose sturgeon ranged from 487 to 788 mm fork length, 500–2400 g weight, and 5–20 years of age, whereas spawning blue sucker ranged from 495 to 822 mm total length, 900–5100 g weight, and 5–34 years of age, although age estimates were uncertain. Females were significantly larger than males for both species although there was overlap. Growth in length was negligible for tagged and recaptured presumably spawning shovelnose sturgeon and low (3.5 mm/y) for blue sucker, suggesting that nearly all growth may have occurred prior to maturity and that fish may have matured at a wide range of sizes.     

Contrasting effects of functionally distinct tadpole species on nutrient cycling and litter breakdown in a tropical rainforest stream

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Sequence of ontogenetic development and atrophy of the oral apparatus of six anuran tadpoles

The development of the oral structures of six species of anuran tadpoles with four different types of mouth parts and the metamorphic atrophy of these structures in two species with different mouth parts are described. The oral labia of typical tadpoles, oral flaps of microhylids, and lateral oral folds of Rhinophrynus are assumed to be homologous. We also suggest that the barbels of the tadpoles of Rhinophrynus are homologs of the marginal papillae of species with an oral disc. Developmental patterns and sequences of the oral structures of all tadpoles examined follow a common pattern: stomodeal invagination, oral pad development, jaw sheeth delimitation, tooth row ridge development, jaw sheath keratinization, and labial tooth keratinization. Developmental patterns remain constant, while interspecific differences are apparent because of truncations of ontogeny at specific stages. Metamorphic atrophy of oral structures occurs roughly in the reverse order of development, although the procedure is rapid and more haphazard than development.     

On the position of the digenean family Heronimidae: an inquiry into a cladistic classification of the Digenea

Brooks, O'Grady & Glen (1985b) placed the seemingly aberrant and highly derived family Heronimidae at the base of their cladogram of the Digenea. In the absence of arguments for the composition and polarity of the putative homologous series on which their cladogram is based, it was found necessary to consider in detail almost all of their character series. In the course of my analysis I (1) argue that the oral sucker is singular to the Digenea, and that the oral sucker is not synapomorphic nor the ventral sucker symplesiomorphic for the Digenea, but that early digeneans lacked both suckers, (2) reiterate that the amphistomate condition is secondary and has arisen more than once, and that the embryology of the excretory system proves it to be secondary in all cases, (3) offer support for Cable's view that the cercarial stylet is not of single origin, and (4) restate the argument that paramphistomes, microscaphidiids, and gyliauchenids have not an oral sucker but a pharynx. Brooks, Bandoni, Macdonald & O'Grady (1989) stated that the bifurcate gut is unambiguously a synapomorph of the Digenea, on the basis of their cladistic demonstration that Rugogaster with a bifurcate gut is a sister group to the rest of the Aspidobothria, which in turn is a sister group to the digenea. Testing this in a new cladogram of the Aspidobothria constructed from Brooks et al.'s (1989) 15 characters (corrected, especially those of the ventral sucker, for which a new phylogeny is advanced), supplemented by an additional 23 characters, reveals Rugogaster as the derived form it appeared to be and aspidogastrids, with a single caecum, as sister group to the rest of the Aspidobothria. A new analysis of the characters produced an increase in homoplasy from 18% to 37%, showed 97 out of 212 characters invalid as used, these two resulting in a decrease in resolution from 82% to 32%, and resulted in changes in polarity in 20 of the 65 putative homologous series listed by Brooks et al. (1985b). The Heronimidae cannot be at the base of their cladogram as it has not three but 13 apomorphs, which is more than have the next three groups, the paramphistomiforms, echinostomatiforms and haploporiforms. Comparison of the Heronimidae with the Bivesiculidae in the light of 48 defensible plesiomorphs shows that the Bivesiculidae, which have 39 of the 48 characters, are more plesiomorphic than the Heronimidae, which have only 23. In conclusion, what remains of the data-base is insufficient to support their cladogram and classification. Better data from the flukes themselves are necessary for a sound cladistic analysis.