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The lateral line system in anurans is functional during aquatic stages and therefore could provide characters related to larval morphological variation. However, few studies have addressed its components in an integrated overview, and little is known about its ontogenetic variation. This study describes the postembryonic trajectory of the lateral system in Telmatobius atacamensis up to its metamorphic regression. This includes structure, number, topography, and innervation of neuromasts, to contribute new and complete information about its larval organization and its temporal sequence of regression. The arrangement and innervation of lateral lines in T. atacamensis resembles those described for other Type IV tadpoles. Its distinctive features are the orientation of the neuromast stitches in the lateral lines, the presence of supraotic neuromasts, and the first-described case of asymmetry of the ventral trunk line. The temporal sequence of regression during metamorphosis differs between the lateral lines and the lateral line nerves, which remain myelinated into postmetamorphic stages. This asynchronous pattern between different components of the system has also been described for Pseudis paradoxa, which shares with T. atacamensis a remarkably long larval period. This long larval period and gradual metamorphosis could also be related to the constitutive metamorphic regression of the system, in spite of the aquatic lifestyle of these frogs.

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This study describes the cephalic and trunk lateral line systems in Patagonian blenny Eleginops maclovinus juveniles, providing morphological details for pores, canals and neuromasts. Eleginops maclovinus juveniles possess a complete laterodorsal lateral line that extends from the upper apex of the gill opening along the trunk as far as the caudal fin. The lateral line was ramified through pores and canals. The following pores were recorded: four supraorbital pores, with two along the eye border and two on the snout; seven infraorbital pores, with three on the lacrimal bone and four being infraorbital; five postorbital pores, with three along the preopercular border (upper preoperculum branch) and two on the bone curvature (inferior preoperculum branch); and four mandibular pores aligned along the jaw. Furthermore, five narrow-simple and interconnected canals were found (i.e. preopercular, mandibular, supraorbital and infraorbital canals). Histologically, the dorsal lateral line presented thin neuromasts (350 µm) with short hair cells. By contrast, the cranial region presented long, thick neuromasts. Infraorbital and mandibular neuromasts had a major axis length of 260 µm and respective average diameters of 200 and 185 µm. Sensory system variations would be due to a greater concentration of neuromasts in the cranial region, allowing for a greater perception of changes in water pressure. Scarce morphological information is available for the lateral sensory system in Eleginopsidae, particularly compared to Channichthyidae, Bovichthydae, Artedidraconidae and Bathydraconidae. Therefore, the presented results form a fundamental foundation of knowledge for the lateral-line system in juvenile E. maclovinus and provide a basis for future related research in this taxon as well as within the Notothenioidei suborder.

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A new species of Pimelodella is described from several right-bank tributaries of the Rio Madeira basin in Amazonas and Rondônia states, Brazil. The new species differs from all congeners by the supraoccipital process not reaching the anterior nuchal plate, 43-45 total vertebrae, maxillary barbels reaching between adpressed anal-fin terminus and caudal-fin origin, epiphyseal branch of supraorbital laterosensory canal emerging as two distantly-positioned pores and a conspicuous black mark at distal third of dorsal fin, between dorsal-fin spine and third branched ray. A detailed description of the cephalic laterosensory system of the new species is provided and contrasted with other Siluriformes and Ostariophysi. A discussion regarding homology of the catfish upper pectoral girdle bones is offered in light of modifications of the postotic and supratemporal lateral-line canals. Based on the placement of the pterotic branch of the postotic canal, it is concluded that the extrascapula is fused to the pterotic in Siluriformes. Results presented herein offer an example of how lateral-line morphology can be used as a compelling source of evidence to help determine homology of cranial and upper pectoral girdle bones.

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Fish commonly use their lateral line system to detect moving bodies such as prey and predators. A remarkable case is the Mexican blind cavefish Astyanax fasciatus, which evolved the ability to detect non-moving obstacles. The swimming body of A. fasciatus generates fluid disturbances, the alteration of which by an obstacle can be sensed by the fish's lateral line system. It is generally accepted that these alterations can provide information on the distance to the obstacle. We observed that A. fasciatus swimming in an unfamiliar environment open and close their mouths at high frequency (0.7-4.5 Hz) in order to generate suction flows. We hypothesized that repeated mouth suction generates a hydrodynamic velocity field, which is altered by an obstacle, inducing pressure gradients in the neuromasts of the lateral line and corresponding strong lateral line stimuli. We observed that the frequency and rate of mouth-opening events varied with the fish's distance to obstacles, a hallmark of pulse-based navigation mechanisms such as echolocation. We formulated a mathematical model of this hitherto unrecognized mechanism of obstacle detection and parameterized it experimentally. This model suggests that suction flows induce lateral line stimuli that are weakly dependent on the fish's speed, and may be an order of magnitude stronger than the correspondent stimuli induced by the fish's gliding body. We illustrate that A. fasciatus can navigate non-visually using a combination of two deeply ancestral and highly conserved mechanisms of ray-finned fishes: the mechanism of sensing water motion by the lateral line system and the mechanism of generating water motion by mouth suction.

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A new species of Gephyrocharax is described from the río Cascajales basin, a tributary of the río La Colorada, río Magdalena system, Colombia. The new species is distinguished from its congeners, except G. melanocheir, by the absence of an adipose fin in most specimens and by the possession of a lateral branched pectoral-fin ray in males with a distal fan-shaped structure with minute bony hooks and a dark blotch or a few scattered dark brown chromatophores along its branches. The new species differs from G. melanocheir by the absence of an intense black pigmentation at the base of the anterior five dorsal-fin rays, the number of vertebrae (40-41 vs. 38-39), the frontals contacting each other anterior to the epiphyseal bar in adults (vs. the absence of contact), the posterior margin of the mesethmoid straight in its central portion (vs. strongly concave at this point), the pouch scale of mature males reaching caudal-fin ray 11 or the area between caudal-fin rays 11 and 12 (vs. reaching only to caudal-fin ray 10 or the area between caudal-fin rays 9 and 10), the number of minute terminal branches of the lateral branched pectoral-fin ray of mature males (60-88 vs. 28-54), a longer black lateral stripe along the body in males (reaching to the base of the caudal-fin rays vs. reaching the middle of the length of the caudal peduncle), and the snout length (28.3-31.8% HL vs. 22.2-28.0% HL). The diagnosis of Gephyrocharax is modified to include species with the adipose fin variably present.

Una nueva especie del género Gephyrocharax se describe para la cuenca del río Cascajales, tributario del río La Colorada, sistema del río Magdalena, Colombia. La nueva especie se distingue de sus congéneres, excepto G. melanocheir, por la ausencia de aleta adiposa en la mayoría de los individuos y por la presencia del radio ramificado lateral de la aleta pectoral con una estructura distal en forma de abanico, la cual tiene ganchos óseos diminutos y una mancha difusa oscura o unos pocos cromatóforos pardos oscuros a lo largo de sus ramificaciones. La nueva especie difiere de G. melanocheir por la ausencia de una intensa pigmentación negra sobre la base de los cinco radios anteriores de la aleta dorsal, el número de vértebras (40-41 vs. 38-39), los frontales contactando entre sí anteriormente a la barra epifisaria en adultos (vs. la ausencia de contacto), el margen posterior del mesetmoides recto en su porción central (vs. fuertemente cóncavo en este punto), la extensión dorsal de la escama-bolsillo de machos maduros alcanzando el radio caudal 11 o el área entre los radios caudales 11 y 12 (vs. alcanzando el radio caudal 10 o el área entre los radios caudales 9 y 10), el número de ramificaciones terminales diminutas del radio ramificado lateral de la aleta pectoral (60-88 vs. 28-54), la línea negra lateral sobre el cuerpo en machos más alargada (alcanzando la base de los radios de la aleta caudal vs. alcanzando la mitad de la longitud del pedúnculo caudal), y la longitud del hocico (28,3-31,8% LC vs. 22,2-28,0% LC). Modificamos la diagnosis de Gephyrocharax incluyendo especies con o sin aleta adiposa.

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A new species of Gephyrocharax is described from the río Cascajales basin, a tributary of the río La Colorada, río Magdalena system, Colombia. The new species is distinguished from its congeners, except G. melanocheir, by the absence of an adipose fin in most specimens and by the possession of a lateral branched pectoral-fin ray in males with a distal fan-shaped structure with minute bony hooks and a dark blotch or a few scattered dark brown chromatophores along its branches. The new species differs from G. melanocheir by the absence of an intense black pigmentation at the base of the anterior five dorsal-fin rays, the number of vertebrae (40-41 vs. 38-39), the frontals contacting each other anterior to the epiphyseal bar in adults (vs. the absence of contact), the posterior margin of the mesethmoid straight in its central portion (vs. strongly concave at this point), the pouch scale of mature males reaching caudal-fin ray 11 or the area between caudal-fin rays 11 and 12 (vs. reaching only to caudal-fin ray 10 or the area between caudal-fin rays 9 and 10), the number of minute terminal branches of the lateral branched pectoral-fin ray of mature males (60-88 vs. 28-54), a longer black lateral stripe along the body in males (reaching to the base of the caudal-fin rays vs. reaching the middle of the length of the caudal peduncle), and the snout length (28.3-31.8% HL vs. 22.2-28.0% HL). The diagnosis of Gephyrocharax is modified to include species with the adipose fin variably present.(AU)

Una nueva especie del género Gephyrocharax se describe para la cuenca del río Cascajales, tributario del río La Colorada, sistema del río Magdalena, Colombia. La nueva especie se distingue de sus congéneres, excepto G. melanocheir, por la ausencia de aleta adiposa en la mayoría de los individuos y por la presencia del radio ramificado lateral de la aleta pectoral con una estructura distal en forma de abanico, la cual tiene ganchos óseos diminutos y una mancha difusa oscura o unos pocos cromatóforos pardos oscuros a lo largo de sus ramificaciones. La nueva especie difiere de G. melanocheir por la ausencia de una intensa pigmentación negra sobre la base de los cinco radios anteriores de la aleta dorsal, el número de vértebras (40-41 vs. 38-39), los frontales contactando entre sí anteriormente a la barra epifisaria en adultos (vs. la ausencia de contacto), el margen posterior del mesetmoides recto en su porción central (vs. fuertemente cóncavo en este punto), la extensión dorsal de la escama-bolsillo de machos maduros alcanzando el radio caudal 11 o el área entre los radios caudales 11 y 12 (vs. alcanzando el radio caudal 10 o el área entre los radios caudales 9 y 10), el número de ramificaciones terminales diminutas del radio ramificado lateral de la aleta pectoral (60-88 vs. 28-54), la línea negra lateral sobre el cuerpo en machos más alargada (alcanzando la base de los radios de la aleta caudal vs. alcanzando la mitad de la longitud del pedúnculo caudal), y la longitud del hocico (28,3-31,8% LC vs. 22,2-28,0% LC). Modificamos la diagnosis de Gephyrocharax incluyendo especies con o sin aleta adiposa.(AU)

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