Genetic and physiological studies of ovulation rate, both natural and induced, in a random bred population of laboratory mice led to the following results.(1) The heritability of natural ovulation rate in nulliparous females was 22±19%, estimated from the correlation between paternal half-sibs.(2) Selection applied to natural ovulation in primiparous females led to a response in both directions, with a realized heritability of 31% (h2 within litters = 0·18 ± 0·013). The number of eggs shed by the High, Control and Low lines after 12 generations were respectively 21, 16 and 14.(3) Selection applied to ovulation induced by 4 i.u. of PMS led also to a response in both directions, with a realized heritability of 22% (h2 within litters = 0·11 ± 0·038). The induced ovulation rates of the High, Control and Low lines after 12 generations were respectively 29, 19 and 14 eggs.(4) PMS-equivalents were calculated from dose-response curves, and were found to be nearly the same in all lines except the line selected for high natural ovulation rate, which had a PMS-equivalent nearly double that of the Control. From this it was inferred that the increase of ovulation rate resulting from selection for high natural ovulation was due to an increased FSH activity, whereas the changes of ovulation rate resulting from selection for low natural ovulation and for both high and low induced ovulation were due to changes of ovarian sensitivity.(5) Genetic correlations, estimated from correlated responses to selection, were: (i) between natural and induced ovulation in primiparous females, 0·33; (ii) between primiparous and nulliparous females in natural ovulation, 0·46; (iii) between primiparous and nulliparous females in induced ovulation, 0·82.(6) The selection for induced ovulation produced changes in litter size following natural ovulation that were nearly equal to the changes in natural ovulation rate. The selection for natural ovulation, however, produced no clear changes of litter size.

The patterns of seasonal variation in reproductive activity were observed over a period of 15 mo for approximately 15 females of each of three breeds: Finnish Landrace (Finn), Tasmanian Merino (Merino) and Scottish Blackface (Blackface). The incidence of oestrus was measured by teasing with vasectomized rams, and the incidence and rate of ovulation were determined frequently by laparoscopy. Luteal function was assessed from peripheral venous blood progesterone concentration on days 7 and 11 of the oestrous cycle. Nutritional status was monitored by recording body weight and plasma-free fatty acid levels throughout the study.The breeding seasons differed significantly: Finn, October to May; Merino, September to February; and Blackface, October to February. Variation in the incidence of ovulation was similar to that in the incidence of oestrus for each breed. The incidence of silent ovulation varied with the breed, being greatest in the Merino and least in the Finn. The ovulation rate varied among breeds (Finn, 2-99; Merino, 1-08 and Blackface, 1-30), and during the breeding season (e.g. Finn: November, 3-5; March, 2-6). Follicles were observed in each breed throughout the period of study.The pattern of variation in progesterone concentration was similar for each breed despite their different breeding seasons. In addition to breed differences in ovulation rate and in onset and end of the breeding season, the sensitivity to oestrogen was apparently such that, with the Finn if oestrogen secretion was high enough to stimulate ovulation it would usually also stimulate oestrus, whereas with the Merino ovulation often occurred without oestrus; this suggests that in the Merino the centres controlling ovulation are more sensitive to oestrogen than those controlling behaviour.

SUMMARY Seasonal variation in the ovulation rate and incidence of ovulation was examined in 15 Romanov and 15 Solognote ewes by endoscopy. The ovulation rate of the Romanovs was found to be related to the incidence of ovulation (r = 0·78) and to the incidence of oestrus as measured by daily teasing with aproned entire rams (r = 0·83). The ovulation rate of the Romanovs was greater than that of the Solognotes, and was 2·6 and 1·1 corpora lutea in the two breeds, respectively, in the autumn. The durations of the breeding season and of oestrus of the Romanovs exceeded those of the Solognotes. The characteristics of the preovulatory discharge of luteinizing hormone (LH) and the daily plasma LH levels were studied by radioimmunoassay in the Romanov and Solognote ewes and in ewes of the Berrichon and Berrichon × Romanov breeds. The interval between the onset of oestrus and the discharge of LH was greater in the Romanovs (17·6 h) than in the other breeds (mean = 7·5 h). The total release of LH, however, was not related to the number of corpora lutea formed.

The concentrations of oestradiol, androstenedione, progesterone and prostaglandin F2alpha (PGF2alpha) were measured in utero-ovarian autotransplants. The secretion of oestradiol was closely correlated with that of androstenedione (r = 0-67, P less than 0-001) indicating a common origin from the Graafian follicle. The concentration of these two steroids fluctuated at random throughout the luteal phase with the maximum secretion occurring about 2 days before the onset of oestrus. Functional regression of the corpus luteum, as indicated by a fall in the secretion of progesterone, began on day 12 or day 13, i.e. about 4 days before the onset of oestrus. In five of the six cycles the first significant rise in the secretion of PGF2alpha occurred on days 12-14 at the time of decline of progesterone secretion, although the release of PGF2alpha was maximal on the day before the onset of oestrus. There was very little release of PGF2alpha from the uterus before day 12. The temporal relationship of these events suggests that the uterus will only release PGF2alpha after it has been primed for 7-10 days with progesterone. The initiation of luteal regression is independent of secretion of oestradiol by the pre-ovulatory follicle which may, however, stimulate the further release of PGF2alpha responsible for irreversible structural luteolysis on the day of pro-oestrus.

Summary. 'The extent of genetic and environmental variation' in the development of reproduction in sheep is illustrated by examples with particular reference to variation among breeds and to the effects of photoperiod. The interactions between genetic and environmental effects are introduced ; these may be so great that genetic groups may reverse their ranking for rate of development in different environments. The 'physiology of puberty' is then discussed. The difficulty of separating puberty from seasonal variation is stressed, and a possible contrast is drawn between the physiological characteristics of genetic variation and those of environmental variation in reproductive development. Finally the physiological factors associated with sterility in young females are discussed; most studies, however, have been conducted during the time of year when adult females would also be expected to be sterile, so that conclusions are difficult and a 'missing link' cannot be identified.