Phylogenetic position of Trichomycterus astromycterus (Siluriformes: Trichomycteridae), an enigmatic trichomycterid from eastern Brazil, inferred from molecular data.

Recently in this journal, a new trichomycterine from eastern Brazil, Trichomycterus astromycterus, was described and considered possibly related to the Chilean Bullockia maldonadoi due to morphological similarities. Subsequently, osteological data supported T. astromycterus in the subgenus Psammocambeva of Trichomycterus, from eastern Brazil. Phylogenetic analyses, performed here, using a multigene data set for a broad trichomycterine sample, corroborate T. astromycterus as a member of Psammocambeva, reinforcing the importance of molecular data for inferring trichomycterine relationships but showing that osteological data alone may infer correctly phylogenetic placements when using broad comparative databases.

Chromosomal Mapping of Repeat DNA in Bergiaria westermanni (Pimelodidae, Siluriformes): Localization of 45S rDNA in B Chromosomes.

The occurrence of repetitive DNA in autosomes and B chromosomes of Bergiaria westermanni was examined using conventional and molecular cytogenetic techniques. This species exhibited 2n = 56 chromosomes, with intra- and interindividual variation in the number of heterochromatic B chromosomes (from 0 to 4). The 5S rDNA was localized in pairs 1 and 5, and histone probes (H1, H3, and H4) and U2 small nuclear RNA were syntenic with 5S rDNA in pair 5. Histone sequences were also located in chromosome pair 14. The (GATA)n sequence was dispersed throughout the autosomes and B chromosomes, with clusters (microsatellite accumulation) in some chromosome regions. The telomeric probe revealed no signs of chromosomal rearrangements in the genome of B. westermanni. The 45S rDNA sites were detected in the terminal region of pair 27; these sites corresponded to a GC-rich heterochromatin block. In addition, 3 of the 4 B chromosomes also contained 45S rDNA copies. Silver nitrate staining in interphase nuclei provided indirect evidence of the expression of these rRNA genes in B chromosomes, indicating the probable origin of these elements. This report shows plasticity in the chromosomal localization of repeat DNA in B. westermanni and features a discussion of genomic diversification.

Immunohistochemical and ultrastructural evidence of functional organization along the Corydoras paleatus intestine.

The Neotropical catfish, Corydoras paleatus (Callichthyidae) is a facultative air-breathing teleost that makes use of the caudal portion of the intestine as an accessory air-breathing organ. This portion is highly modified, being well vascularized with capillaries between epithelial cells, which makes it well suited for gas exchange. Instead, the cranial portion is a digestion and absorption site, as it has a typical intestinal epithelium with columnar cells arranged in a single row, villi and less vascularized tunica mucosa. Therefore, the intestine was studied by light and electron microscopy to assess differences between the cranial, middle and caudal portions. To characterize the potential for cell proliferation of this organ, we used anti-proliferating cell nuclear antigen antibody and anti-Na(+) K(+) -ATPase monoclonal antibody to detect the presence of Na(+) /K(+) pump. In C. paleatus it was observed that cell dynamics showed a decreasing gradient of proliferation in cranio-caudal direction. Also, the intestine of this catfish is an important organ in ionoregulation: the basolateral Na(+) /K(+) pump may have an active role, transporting Na(+) out of the cell while helping to maintain the repose potential and to regulate cellular volume.

Chilling of Steindachneridionparahybae (siluriformes: pimelodidae) embryos.

The objective of this study was to assess the viability of Steindachneridion parahybae embryos after chilling using different cryoprotectant solutions, stages of embryonic development, chilling curves, and storage periods at temperatures between -10 °C and 0 °C. Three experimental tests were conducted, and the following aspects were evaluated: (1) the toxicity of six cryoprotectant solutions (10% methanol, ethylene glycol, or DMSO combined with 0.5-M sucrose or lactose); (2) viability of embryos submitted to cooling with two cryoprotectant solutions (10% or 20% methanol combined with 10-M sucrose) at three different stages of development (closure of blastoporus, appearance of the optic vesicle and the moment when the tail began to straighten out), and two chilling periods (6 and 12 hours); (3) viability of embryos submitted to cooling with three chilling curves (directly to the freezer without a curve, 0.5 °C/min and 1.0 °C/min) and two chilling periods (6 and 12 hours). After the tests, it was concluded that the protocol which presented the most positive results after chilling, with a hatching rate of 63.50 ± 9.98% of the embryos and 12.32 ± 3.85% normal hatched larvae, was the one with embryos at the free-tail stage, the cryoprotectant solution with 10% methanol and 10-M sucrose, a chilling curve of 0.5 °C/min, stored for a maximum of 6 hours at subzero temperatures (temperature ranging between -5.05 °C and -7.83 °C).

Induced spawning and reproductive variables of the catfish Lophiosilurus alexandri Steindachner, 1876 (siluriformes: pseudopimelodidae)

Lophiosilurus alexandri is an endemic fish from the São Francisco River basin, Brazil. The aim of this study was to induce L. alexandri to spawn and to obtain data on several reproductive variables for this species. For induced spawning, adults were submitted to Cyprinus carpio pituitary homogenate (CPH). Nine of the 12 females (75%) responded positively to the treatment. The stripping of oocytes was performed 8.4 h after the second dose of CPH with the water temperature maintained at 26ºC. The number of stripped oocytes per gram of ova was 74 ± 5 oocytes g-1, and the mean oocyte diameter was 3.1 ± 0.2 and 3.6 ± 0.2 mm, before and after hydration, respectively. The oocytes were opaque, yellowish, demersal, highly adhesive, and covered by a gelatinous coat. The total fecundity was 4,534 ± 671 oocytes, and the fertilization rate was 59%. The initial and final fertilities were 2,631 ± 740 and 1,542 ± 416 embryos, respectively. Larval hatching occurred up to 56 h after fertilization, and the larvae had a total length of 8.4 ± 0.1 mm. This work provides important biological information for L. alexandri that can be used for management and conservation of this species.

Lophiosilurus alexandri é um peixe endêmico da bacia do rio São Francisco, Brasil. O objetivo do trabalho foi induzir L. alexandri à desova e obter dados sobre várias variáveis reprodutivas para esta espécie. Para desova induzida, adultos foram submetidos ao homogeneizado de hipófise de Cyprinus carpio (HHC). Nove das 12 fêmeas (75%) responderam positivamente ao tratamento. A extrusão dos ovócitos aconteceu 8,4 h após a segunda dose de HHC com a temperatura da água mantida a 26ºC. O número de ovócitos liberados por grama de ova foi de 74 ± 5 ovócitos g-1 e a média do diâmetro ovocitário foi de 3,1 ± 0,2 e 3,6 ± 0,2 mm, antes e depois da hidratação, respectivamente. Os ovócitos foram opacos, amarelo-castanho, demersais, altamente adesivos e revestidos por capa gelatinosa. A fecundidade total apresentou 4.534 ± 671 ovócitos e a taxa de fertilização foi de 59%. As fertilidades inicial e final foram de 2.631 ± 740 e 1.542 ± 416 embriões, respectivamente. A eclosão das larvas aconteceu até 56 h após a fertilização e as larvas tiveram comprimento total de 8,4 ± 0,1 mm. Este trabalho fornece informações biológicas importantes para L. alexandri, que podem ser utilizadas para o manejo e conservação desta espécie.

Description of a new species of Ituglanis (Siluriformes: Trichomycteridae) from Serra dos Carajás, rio Tocantins basin

A new species of Ituglanis is described from the rio Tocantins basin, State of Pará, Brazil. Ituglanis ina, new species, is distinguished from its congeners by the presence of a dark vertical bar over the base of the caudal-fin rays (vs. no bars over caudal-fin base); and by the presence of a middle trunk line of tiny neuromasts extending along the flank until the vertical through the dorsal fin, or near the caudal-fin base (vs. no middle trunk line of tiny neuromasts). Ituglanis ina can be further distinguished by a combination of characters related to color pattern and morphology. Comments on the relationship between Ituglanis species are presented.

Uma espécie nova de Ituglanis é descrita da bacia do rio Tocantins, Pará, Brasil. Ituglanis ina, espécie nova, é facilmente diferenciada das congêneres por apresentar uma barra vertical escura sobre a base dos raios da nadadeira caudal (vs. sem barras na base da nadadeira caudal); e por apresentar linha lateral seguida por uma linha de diminutos neuromastos até a região do flanco, abaixo da nadadeira dorsal, ou até o pedúnculo caudal (vs. sem neuromastos após a linha lateral). Ituglanis ina distingue-se, também, por uma combinação de caracteres relacionados ao padrão de coloração e morfologia. Comentários sobre o relacionamento das espécies e grupos de espécies de Ituglanis são apresentados.

Induced spawning and early ontogeny in hatchery-reared catfish Zungaro jahu (Siluriformes: Pimelodidae)

Hatchery-kept catfish jahus Zungaro jahu (Ihering, 1898) were induced to spawn with carp pituitary extract. The telolecithal eggs were round (1.6 ± 0.1 mm in diameter), demersal, free, and covered with a 0.4 mm-thick jelly coat. The gonadosomatic index of 2.8 was comparable to that of other Pimelodidae. The number of eggs x g of ova-1 was 804 ± 144. Hatching occurred 14.5 h after fertilization, at a temperature of 27.3 ± 0.4º C. The newly-hatched embryos measured 3.9-4.3 mm of total length (TL). At 18 h post-hatching (HPH; 5.3 ± 0.1 mm TL), the retina was pigmented, the mouth opened and dorsoflexion of the notochord had initiated. At 36 HPH (6.4 ± 0.2 mm TL), fusiform chromatophores were vertically arranged in the primordial fin fold and the notochord was dorsoflexed. The yolk sac was almost exhausted by 48 HPH (7.3 ± 0.2 mm TL). At 128 HPH (8.6 ± 0.6 mm TL) the pectoral, dorsal, adipose, caudal, anal, and pelvic fins were readily observable whereas the primordial fin fold was no longer visible. At 224 HPH (16.6 ± 2.5 mm TL), the metamorphosis was completed and the larvae had acquired the juvenile appearance.

Jaús Zungaro jahu (Ihering, 1898), mantidos em estação de piscicultura, foram induzidos à reprodução com extrato bruto de hipófise de carpa. Seus ovos são telolécitos, arredondados (1,6 ± 0,1 mm de diâmetro), demersais, livres e cobertos por uma capa gelatinosa com 0,4 mm de espessura. O índice gonadossomático (peso da ova : peso total do peixe) de 2,8 foi semelhante ao de outros Pimelodidae. O número de ovos x g de ova-1 foi 804 ± 144. A eclosão dos embriões ocorreu 14,5 h pós-fertilização à temperatura de 27,3 ± 0,4º C. Os embriões recém-eclodidos apresentaram 3,9-4,3 mm de comprimento total (CT). Dezoito horas pós-eclosão (HPE) e 5,3 ± 0,1 mm CT, a retina estava pigmentada, a boca aberta e a flexão da notocorda tinha se iniciado. Às 36 HPE (6,4 ± 0,2 mm CT), observaram-se cromatóforos fusiformes alinhados verticalmente na nadadeira primordial; a notocorda já se encontrava flexionada. O saco vitelínico encontrava-se quase que inteiramente absorvido às 48 HPE (7,3 ± 0,2 mm CT). Com 128 HPE (8,6 ± 0,6 mm TL), as nadadeiras peitoral, dorsal, adiposa, caudal, anal e pélvica estavam formadas e a nadadeira primordial já havia sido reabsorvida. Com 224 HPE (16,6 ± 2,5 mm CT), a metamorfose se completou e as larvas se transformaram em juvenis.