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Aim: To analyze temporal distribution of larvae and juveniles and the early development and of Moenkhausia cf. gracilima. Methods: Samples were taken quarterly in twenty-five sites in the upper Paraná River floodplain between August 2013 and May 2015. The samples were taken under the water surface at night using 0.5 mm mesh plankton nets. In the laboratory, samples were sorted, identified and separated into larval (preflexion, flexion and postflexion) and juvenile periods. Results: A total of 248 individuals was collected, mainly in the Saraiva Lagoon, suggesting that the entire life cycle of this species occurs in this environment. The reproductive period takes place between December and April, since the postflexion larvae were found until May. However, the occurrence of juveniles between February and May indicates probable batch spawning. Among the 95 individuals used for ontogenic description, 82 were larvae and 13 juveniles. Larvae may be characterized by irregular pigmentation in the upper region of the head, mouth, and body, increasing throughout development; upper lobe of the caudal fin more pigmented than the lower lobe, only visible in postflexion larvae; terminal mouth; anal opening located anterior to the median region of the body and total number of myomers ranging from 34 to 40 (15 to 20 pre and 16 to 23 postanal), while juveniles have characteristics similar to adults. The total number of fin rays is: P. 11-16, V. 7-11, D, 9-11 and A. 21-23. Conclusions: According to the distribution of developmental periods it is possible to conclude that this species reproduces in the summer, preferably in lagoons. Growth analysis indicated important alterations in larval morphology (metamorphosis) that may be associated with the ecomorphological characteristics of the species. The morphological separation of larvae of M. cf. gracilima from other larvae of small characids, especially at preflexion and flexion stages may be complicated by the overlap of traits, suggesting the use of other variables, mainly morphometric, for the separation of the species.

Structural habitat complexity provided by macrophytes is expected to increase richness and abundance of fish species. However, this topic is rarely investigated simultaneously at different periods of fish development. We sampled fish within macrophyte stands and in non‐vegetated areas at floodplain lakes and tested the hypothesis that the presence of macrophytes increases abundance and species richness of fish, in addition to changes in species composition, at different periods of fish development. Our findings demonstrated that, in different period of fish development, the highest values of fish species richness and abundance were found at sites colonised by macrophytes. Similarly, changes in fish species composition were observed between habitats colonised by macrophytes and non‐vegetated areas. Therefore, the results demonstrate that macrophyte presence plays an important role in regulating fish community structure at different periods of fish development.

The Characidium orientale Buckup & Reis, 1997 larvae development is described using specimens collected in the natural environment of Antas River, in the Taquari-Antas river basin, Rio Grande do Sul, Brazil. Were considerate ontogenetic changes in morphology, pigmentation, fin morphology, and meristic characters. Thirty-six larvae (33 in the preflexion stage, two in flexion, and one in the postflexion stage), with a standard length between 4.24 and 11.26 mm were analyzed. The larvae of C. orientale are altricial and present fusiform body, subterminal mouth, long intestine with anal opening posterior to the vertical line over the median region of the body. Two chromatophores are evident in the interorbital region, as well pigments concentrated on the side of the body, forming a longitudinal stripe, and between the rays of the caudal fin, which intensify during the development. Also, a conspicuous remnant of the embryonic membrane (finfold) in front of the dorsal fin appears to be characteristic of species of the genus during larval development. The total number of myomeres varies from 32 to 35 (18-23 pre; 11-16 postanal). The main changes in morphometry occur during the preflexion stage and suggest physiological and behavioral changes.