Results 21 to 30 of about 1,060 (196)
Hyphessobrycon condotensis Regan 1913
, 2020 Hyphessobrycon condotensis Regan, 1913 (Figs. 9–10, Tab. 3) Hyphessobrycon condotensis Regan, 1913: 465 [original description, type locality: “Rio Condoto (…) and the Rio San Juan”, Colombia]—. Eigenmann, 1922: 141 [as a synonym of H.
Ota, Renata R. +2 more
core +3 more sources
A new Hyphessobrycon (Characiformes: Characidae) of the Hyphessobrycon heterorhabdus species-group from the lower Amazon basin, Brazil [PDF]
Neotropical Ichthyology, 2021 A new species of Hyphessobrycon belonging to the Hyphessobrycon heterorhabdus species-group from the lower rio Tapajós, state of Pará, Brazil, is described. The new species is allocated into the Hyphessobrycon heterorhabdus species-group due to its color
Tiago C. Faria +4 more
doaj +9 more sources
Zootaxa, 2020 Faria, Tiago C., Bastos, Douglas A., Zuanon, Jansen, Lima, Flávio C.T. (2020): A new Hyphessobrycon (Characiformes: Characidae) of the Hyphessobrycon heterorhabdus species-group from the Central Amazon basin, Brazil.
Faria, Tiago C. +3 more
core +4 more sources
Revista de Biología Tropical, 2010 El género Hyphessobrycon es uno de los más numerosos y morfológicamente complejos de la familia Characidae, incluye 122 especies válidas, de las cuales 17 están en Venezuela.
Carlos A García-Alzate +2 more
doaj +4 more sources
Hyphessobrycon savagei Bussing 1966
, 2021 Hyphessobrycon savagei Bussing, 1966. Savage’s Tetra; Sardina, Sardinita, Tetra, Tetra de Savage, Sardinita de Savage. Distribution: Global: Middle America; southwestern and southern Costa Rica, Pacific drainages; Costa Rica: Pi and Tr (Pacific), 0 ...
Angulo, Arturo
core +3 more sources
Hyphessobrycon uaiso: new characid fish from the rio Grande, upper rio Paraná basin, Minas Gerais State (Ostariophysi: Characidae), with a brief comment about some types of Hyphessobrycon [PDF]
Neotropical Ichthyology, 2013 Hyphessobrycon uaiso is described from the upper rio Paraná basin, rio Grande drainage, Minas Gerais State. The new species differs from its congeners by the short anal fin with 12-17 branched rays, and dorsal fin with ii,7-8 rays.
Fernando R. Carvalho, Francisco Langeani
doaj +2 more sources
Hyphessobrycon Durbin in Eigenmann 1908
, 2018 Hyphessobrycon 1. Dorsal fin with black blotch and distal edge of the rays hyaline; black humeral blotch large and conspicuous........................................................................................ H. eques 1’.
Deprá, Gabriel de Carvalho +3 more
core +3 more sources
Hyphessobrycon savagei Bussing 1967
, 2020 Hyphessobrycon savagei Bussing, 1966 (Figs. 19–20, Tab. 6) Hyphessobrycon savagei Bussing, 1966: 215 [original description, type locality: “ Puntarenas: Río Ceibo (260m) at IH, 6 km W of Buenos Aires turnoff”]—.
Ota, Renata R. +2 more
core +3 more sources
Characterization of Mitochondrial Genomes and Evolutionary Relationships in Two <i>Moenkhausia</i> (Characiformes: Acestrorhamphidae). [PDF]
Ecol EvolThis study successfully decoded the complete mitochondrial genomes of two Moenkhausia species, with total lengths of 16,439 and 16,461 bp, respectively. This study enhances genomic resources for Acestrorhamphidae and provides a foundation for investigating evolutionary mechanisms and developing molecular markers.
Sun CH, Chen XD, Zhan YJ, Xu Y, Lu CH.
europepmc +2 more sources
Establishing new grid-size-dependent attributes to rank areas of endemism for conservation priorities. [PDF]
CladisticsAbstract Delineating Areas of Endemism (AEs) is crucial for identifying priority areas for biodiversity conservation in a spatial planning framework. Endemicity Analysis in the NDM/VNDM software is one of the primary methodologies for its delineation.
Frota A, da Graça WJ.
europepmc +2 more sources