4.4 Article

Production of live young with cryopreserved sperm from the endangered livebearing fish Redtail Splitfin (Xenotoca eiseni, Rutter, 1896)

期刊

ANIMAL REPRODUCTION SCIENCE
卷 196, 期 -, 页码 77-90

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.anireprosci.2018.06.021

关键词

Sperm cryopreservation; Ovarian development; Goodeidae; Motility; Fish conservation; Artificial insemination

资金

  1. National Institutes of Health, Office of Research Infrastructure Programs [R24-OD010441, R24-OD011120]
  2. National Institute of Food and Agriculture, United States Department of Agriculture [LAB94231]
  3. LSU-ACRES (Audubon Center for Research of Endangered Species) Collaborative Project [1617R0434]

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Previous studies of sperm cryopreservation of livebearing fish have been limited to two genera within the family Poeciliidae. The goal of the present study was to investigate the feasibility to produce live young of livebearing goodeids (family Goodeidae) with cryopreserved sperm, using aquarium-trade populations of the endangered species Redtail Splitfin (Xenotoca eiseni, Rutter, 1896). Reproductive condition of females was evaluated by histological categorization of ovarian development. A total of 117 females were inseminated with cryopreserved sperm, 81 were inseminated with fresh sperm, 27 were mixed with males for natural breeding, and 30 were maintained without males or insemination. Histological images of 34 mature females indicated 68% of ovaries had primary- or secondary-growth oocytes, and 32% had ovulated eggs. Ovarian development had no significant relationship (P = 0.508) with body wet weight, but had a relationship (P < 0.001) with ovary weight and gonadosomatic index. Sperm cells were observed within ovaries that were fixed at 12 h after insemination with fresh sperm. A total of 29 live young were produced from two females inseminated with thawed sperm (8% post-thaw motility with HBSS300 as extender, 20 min incubation in 15% DMSO, cooling rate at 10 degrees C/min, and thawing at 40 degrees C for 7 s), 12 were produced from two females with fresh sperm (1%-20% motility), 41 were produced from five naturally spawned females, and no live young were produced from the female-only group. This study provides a foundation for establishment of germplasm repositories for endangered goodeids to assist conservation programs.

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