Summary. The development of a sensitive enzyme-immunoassay for 20\g=a\-dihydroprogesterone (20\g=a\-DHP) and its use in determining reproductive status in black and white rhinoceroses is reported. 20\g=a\-DHP in hydrolysed urine diluted in parallel to standards, and high-performance liquid chromatography (HPLC) confirmed the presence of 20\ g=a\ \ x=r eq-\ DHP and the absence of pregnanediol-3\g=a\-glucuronide(PdG) in urine collected from rhinoceroses after oestrus. Conjugated oestrone was identified by HPLC as the major urinary oestrogen in the black rhineroceros and conjugated oestradiol-17\g=b\ was the most abundant in the white rhinoceros. In African species, the black (Diceros bicornis), and northern (Ceratotherium simum cottoni) and southern (Ceratotherium simum simum) white rhinoceroses, excretion of 20\g=a\-DHP and oestrogen followed a cyclic pattern. Excretion of 20\g=a\-DHP was low before mating, at the time of peak oestrogen excretion, but high after oestrus. In the black rhinoceros, the follicular phase was 3\ p=n-\ 4 days and the luteal phase was 18 days, suggesting a cycle of 21\p=n-\22 days. The interoestrus interval in the northern subspecies of white rhinoceros was 25 days, which correlated well with the interval between peaks of oestradiol-17\g=b\ excretion. The interval between urinary oestrogen peaks in the southern subspecies of white rhinoceros suggested a cycle length of 32 days. This paper provides the first description of the pattern of excretion of urinary oestrogens and progesterone metabolites in African rhinoceroses.