Mature males and females of Leporinus piau (Fowler, 1941) were induced to reproduce through a hypophysation process. Extrusion occurred 12 h or 312 hours-degree after the hypophysation, at a water temperature of 26°C. Fertilized eggs were maintained in incubators at 24°C. Embryonic development, was evaluated using every 10 minutes, fresh egg samples which were analyzed under stereoscopic microscope. The larvae were collected at 24-hour intervals for seven days after hatching, fixed in Bouin's fluid and were submitted to routine histological techniques. The eggs of L. piau were slightly gray, non-adhesive and round-shaped. After 1.5 h the embryo was at the 64-blastomere phase and showed a wide yolk region on the vegetative pole. Within 6.25 h, blastopore closure and the end of gastrula was observed. The differentiation of layers occurred after 7.5 h and hatching after 21 h after fertilization at 24°C or 504 hours-degree. During the first three days of the larvae development there was a gradual yolk sac reduction until its complete absorption on the fourth day, indicating the necessity of exogenous feeding. From the fourth to the seventh day, the final development of the heart, gill arches, swimblader, kidney, hepatopancreas, stomach and intestine were observed. The embryonic and larval development of L. piau were similar to other Anastomidae species.

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To study reproduction and embryogenesis, Pimelodus maculatus specimens were kept in captivity and captured bimonthly during 1 year. Gonads samples (211 specimens) were collected and submitted to routine histological techniques. Pimelodus maculatus prepared to reproduce when water temperature was high, and even reached advanced maturation but did not spawn in captivity. Spent fish gonads were not documented, and atretic follicles were frequent (60%) in late maturation females. When then submitted to hypophysation, 70% of the females responded positively to hormonal treatment. Oocyte extrusion occurred 8 h after a second hormonal injection at 26°C. The fertilisation rate was 65.1 ± 9.2% at 24°C. Recently spawned oocytes of P. maculatus were spherical, non-adhesive, yellow in colour, with an average diameter of 1113.92 ± 37.02 μm and covered by a thick gelatinous layer. Blastopore closure occurred 7 h and 30 min after fertilisation. Embryonic development was completed within 18 h after fertilisation. The results of this work provide important knowledge for the handling and cultivation of not only P. maculatus, but other species of potential value for fish culture.

Volunteers were able to match photographs of the same common carp Cyprinus carpio taken on two occasions. Images were identified correctly on 95·76% of occasions. Thus, scale patterns can be used for non-invasive identification of C. carpio over a period of time.

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