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Distal ulna metaphyseal osteochondrosis was identified in seven captive bred cheetahs raised in Australia between 1984 and 2005. The disorder was characterized by bilateral carpal valgus conformation. In the metaphyseal region of the distal ulnae, an osteolucent defect that appeared as a proximal extension of the lucent physis was identified radiographically between 6 and 10 months of age. Ulna ostectomy was done to correct the angular limb deformity. Histologically, changes were identified in the osteolucent lesion that resembled osteochondrosis. We propose that the condition is probably familial and/or dietary in origin.

In December 2008, a southern white rhinoceros (ãsimum simum) aborted a 7-mo gestation male fetus. On hematoxylin and eosin-stained sections of fetal tissues, foci of necrosis were noted in the hepatic parenchyma and were associated with low numbers of lymphocytes, plasma cells, and neutrophils. Protozoal zoites were identified within the hepatic lesions and within the cerebellum. Evaluations utilizing immunohistochemistry, polymerase chain reaction, and DNA sequencing identified the protozoan as Neospora caninum. A microsatellite analysis using MS10 marker showed a unique trinucletoide repeat pattern (ACT), (AGA)19 (TGA)8 distinct from all studied N. caninum to date. This is the first report of N. caninum-related abortion of a rhinoceros fetus of any species and the first report of polymerase chain reaction-confirmed N. caninum infection in any rhinoceros.

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Flow cytometric sexing of spermatozoa followed by application in artificial insemination or in vitro fertilization provides a unique opportunity to predetermine the sex of offspring and might enhance the conservation management of endangered species in captivity such as the elephant and rhinoceros. To obtain an indication of the sortability of spermatozoa from these species, the relative DNA differences between X and Y chromosome bearing spermatozoa (fresh, frozen thawed, epididymal) from three rhinoceros species [white (Ceratotherium simum), black (Diceros bicornis), Indian (Rhinoceros unicornis)] and both elephant species, the Asian and the African elephant (Elephas maximus, Loxodonta Africana), were determined through separation of spermatozoa into X and Y chromosome bearing populations, using a modified high speed flow cytometer. The head profile areas of spermatozoa from all five species were measured using light microscopy. By multiplying the relative DNA differences and the head profile areas, the sperm sorting indices were calculated to be 47, 48 and 51 for white, black and Indian rhinoceros respectively. The calculated sorting index for the Asian elephant was 66. In the African elephant, we determined the highest sorting index of 76. These results indicate the practicability of flow cytometric sex sorting of spermatozoa from the tested rhinoceros species and both elephant species. The lower sorting indices in rhinos indicate that sex sorting of spermatozoa from the rhinoceros will be more challenging than in elephants.