Testes were collected from 2 hunted rhinoceros bulls in Tswalu Desert Reserve in the Kalahari. One was breeding, the other non-breeding. Testes were collected 1 hour after death, transported on ice, and processing began 3 hours thereafter. Sperm were frozen in 0.25 ml straws at 150 million sperm/ml. Straws were cooled to 4 degress and equilibrated for 6 hours. Sperm treatments were evaluated for progressive motility at pre-freeze and at post-thaw. There was a marked difference in motility between breeding and non-breeding male rhinos. There was a noticeable difference between epipidymides of the breeding male, with one epipidymis being half the size of the other, which contained no sperm. No detectable difference in sperm morphology between the 2 bulls. The results suggest that Triladyl +5% FCS would be suitable for freezing the sperm of a white rhino breeding male.
Lubbe, K.; Smith, R.L.; Bartels, P.; Godke, R.A. 1999. Freezing epididymal sperm from white rhinoceros (Ceratotherium simum) treated with different cryodiluents. Johannesburg, Wildlife Breeding Resource Centre, poster presentation. 1.
Freezing epididymal sperm from white rhinoceros (Ceratotherium simum) treated with different cryodiluents
Note
Location
South Africa
Subject
Reproduction
Species
Black Rhino (bicornis)