Lopes, Tais da S. [UNESP]Romagosa, Elizabeth [UNESP]Streit, Danilo P. [UNESP]Ribeiro, Ricardo P. [UNESP]Digmayer, Melanie [UNESP]2014-05-202014-05-202011-02-01Theriogenology. New York: Elsevier B.V., v. 75, n. 3, p. 570-576, 2011.0093-691Xhttp://hdl.handle.net/11449/42253The objective of this research was to verify the effects of cooling embryos of pacu, Piaractus mesopotamicus, in four stages of development during two stocking periods. The stages of embryo development were at: blastoderm, similar to 64 cells-1.4 h after fertilization (haf); 25% of the epiboly movement-5.2 haf; blastoporous closing-8.0 haf; and optical vesicle appearing-13.3 haf. Embryos were exposed to a cryoprotectant solution containing methanol (10%) and sucrose (0.5 M). Thereafter, embryos were submitted to a cooling curve until they reached -8 degrees C, and then kept cooled for 6 or 10 h. In addition, for each stage of embryonic development, a control group with uncooled embryos was used to compare hatching rates. The total number of larvae from the first two stages of ontogenetic development (1.4 and 5.2 haf) was lower compared to the other stages (0.0 and 8.0 haf). There was no significant difference between stages 8.0 and 13.3 haf for the total number of larvae (49.9 +/- 6.7% and 55.2 +/- 6.7%, respectively). Embryo diameter varied according to embryonic stage, providing evidence of differences in membrane permeability. There was a negative correlation between embryo diameter and the total number of larvae (r = -0.372). In conclusion, use of embryonic stages 8.0 and 13.3 haf were recommended for maintaining cooled pacu embryos at -8 degrees C for 6 or 10 h. (C) 2011 Elsevier B.V. All rights reserved.570-576engCryopreservationOntogenetic developmentSouth American fishesLarvae survival ratesArtigo10.1016/j.theriogenology.2010.09.030WOS:000286716400019Acesso restrito