Changes during puberty were studied in the live ram lamb by collecting electro-ejaculates and measuring fructose and citric acid concentration and sperm density and morphology. Fructose and citric acid secretion preceded spermatogenesis. Sperm motility improved with decreasing numbers of abnormal spermatozoa. Observations are included on the separation of the penis from the prepuce. In addition, the influence of season of birth on lamb ejaculates was studied. Reproductive development in lambs born in late summer was delayed, androgen secretion being more markedly affected than spermatogenesis.The results of these studies support the view that the onset of male puberty coincides with the time when the testes become androgenically active, the accessory glands begin to secrete fructose and citric acid, and the animal exhibits characteristic male behaviour. to study the effect of birth date on sexual function. Six of these lambs were born in February/March, and will be referred to as spring lambs, and six were born in July/August and will be referred to as late summer lambs. Data from six mature Suffolk rams have been included for comparison. The lambs were weaned at 3 \ months when supplementary creep feeding was provided at a rate of ¿ lb pelleted concentrates per day (Diet 302, BOCM Ltd).Semen was collected by electrical stimulation (Rowson & Murdoch, 1954) at weekly intervals, using a polypropylene probe 25 cm long and 2 cm diameter, with four embedded brass electrodes, 7 cm long and 0-5 cm wide, alternately connected; the probe was inserted to a depth of about 12 cm inside the anus. Attempts to collect semen by electro-ejaculation were made from 30 days of age onwards. In the spring lambs, Suffolk and cross-bred, these attempts were successful at 42 days of age but in the late summer lambs not until 63 days of age. The total ejaculate was obtained, the appearance noted and volume recorded at weekly intervals.Immediately after collection, a sample of semen was examined under the microscope for the presence of spermatozoa and to observe their motility. If no spermatozoa were present the ejaculate was frozen in solid C02. When spermatozoa first appeared samples were taken after complete ejaculation for nigrosin-eosin staining (Campbell, Dott & Glover, 1956) and haemocytometer counts. When sperm density increased, the bulk of the ejaculate was collected into test tubes in dry ice but a small volume was collected into a separate tube for staining and counting. The percentage of live spermatozoa was determined from the nigrosin-eosin stained slides as well as the morphologi¬ cal abnormalities as classified by Blom (1950).Fructose and citric acid determinations were carried out according to the methods of Roe (1934) and Speck, Moulder, & Evans (1946), respectively, as modified by Mann (1946Mann ( , 1964 and Mann, Davies & Humphrey (1949). Estimations were made on samples of seminal plasma after centrifugation to remove the spermatozoa so that the estimates were made on the same volume of seminal plasma in each case.Obs...