Efeito da restrição alimentar no desempenho reprodutivo de machos de matrinxã Brycon cephalus

Detalhes bibliográficos
Ano de defesa: 2002
Autor(a) principal: Sanabria Ochoa, Ana Isabel [UNESP]
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Estadual Paulista (Unesp)
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Link de acesso: http://hdl.handle.net/11449/144145
http://www.athena.biblioteca.unesp.br/exlibris/bd/cathedra/12-09-2016/000196684.pdf
Resumo: The present study was performed in the Aquaculture Center of the University of São Paulo State, Jaboticabal, SP. Two experiments evaluated the effect of moderate and alternate food restriction on seminal characteristics and reproductive performance of matrinxã (Brycon cephalus). In the first experiment, adult males were distributed into 2 groups. One of them received ration daily (G1, control) and the other (G2, experimental) was fed alternately (fed 3 for days, starved 2 for days) for 3 months during the gonadal maturation. Each group was allotted into 2 earthen ponds (10 fish each) and after 3 months of treatment, males were induced to reproduction with carp pituitary extract (CPE) (1 mg kg-1). After 150 hour/degree, the males were anesthetized (benzocaine, 0.1g/L-1) and semen from each fish were collected by abdominal massage to measure the volume and the spermatocrit in capillary tubes. After that, through microscopy, the cell motility, number of live cells and cell concentration in Neubauer Chamber were determined. A fertilization test was also performed utilizing oocytes from one single female fed daily and CPE induced. Oocytes were divided into 14 samples and fertilized with semen from every male individually. They were incubated in 20L plastic boxes under constant water aeration. Fertilization rate was determined 7 h after fertilization. Hatching rate was also registered and larvae were observed until the yolk sac resorption (72 h after hatching), being collected and fixed to weight and length measurement. Spermatic volume was higher in G2 (9.29 ± 3.31 ml) than in G1 (6.14 ± 1.10 ml), while the motility was similar in both groups (5.00). Cell concentration were also similar in both treatments (6.79 ± 1.16 and 6.65 ± 1.37 cell 106 μL-1, in G1 and G2, respectively), as well as the spermatocrit (13.07 ± 1.99 % in G1 and 13.86 ± 2.87 % in G2). Live cells number did not differ ...