Chilling of Steindachneridionparahybae (siluriformes: pimelodidae) embryos

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Data

2015-09-01

Autores

Lopes, Taís da Silva
Sanches, Eduardo Antônio [UNESP]
Okawara, Renan Yoshiharu
Romagosa, Elizabeth

Título da Revista

ISSN da Revista

Título de Volume

Editor

Elsevier B. V.

Resumo

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).

Descrição

Palavras-chave

Cryopreservation, Cryoprotectant solution, Endangered fish, Neotropical catfish, Ontogenetic development, Preservation of embryo

Como citar

Theriogenology, v. 84, n. 4, p. 538-544, 2015.