Concentrations of progesterone in peripheral plasma of red deer hinds were basal (< 1 ng/ml) during lactation/seasonal anoestrus, but increased abruptly at the onset of the breeding season. Lactating hinds (N = 19) started ovarian cycles 10 days later (P<0\m=.\01) and conceived 16 days later (P< 0\m=.\001) than did 13 weaned hinds. There was no evidence, from plasma progesterone values, of silent oestrus at the start of the season. Progestagen/PMSG treatment induced early ovulations in 8 anoestrous hinds but fertility was low, only 2 conceiving and giving birth. Pregnant hinds (N = 42) had high plasma concentrations of progesterone (mean 3\p=n-\5 ng/ml) which declined just before parturition.

Two experiments were conducted to examine the effects of supplementation of a control diet of barley grain and barley straw containing 4 mg copper (Cu)/kg dry matter (D.M.) either with 5 mg molybdenum (Mo)/kg D.M. or with 500 or 800 mg iron (Fe)/kg D.M. on puberty, fertility and oestrous cycles of cattle. Puberty occurred normally in control, Fesupplemented and control animals on a restricted intake whereas it was delayed by 12 and 8 weeks respectively by Mo supplementation. This effect of Mo was not due to the low Cu status since this was equally low in the Fe-supplemented animals, nor was it due to the reduced growth rate since puberty occurred normally in control animals that had a similar live-weight gain. A significant reduction in the pulsatile release of luteinizing hormone was observed within 11 weeks of the Mo supplementation and before any of the other clinical signs were evident, suggesting that Mo may be affecting puberty by altering the release of luteinizing hormone either directly or indirectly.Mo supplementation significantly reduced the percentage conception rate to 12-33% compared with 57-80% in control and Fe-supplemented animals. This effect was not dependent on the rate of live-weight gain which was standardized across the different treatments at approximately 0 -6 kg/day. Within 12 weeks of the replacement of dietary Fe by Mo a lower conception rate occurred; replacing dietary Mo by Fe led to a normal conception rate within 12 weeks without any accompanying changes in Cu status or in the rate of live-weight gain. The plasma Mo concentrations, however, changed significantly during these alterations in dietary supplementation. The pre-ovulatory peak height of luteinizing hormone was significantly lower in animals on the Mo-supplemented diet compared with control and Fe-supplemented animals, but the administration of LHRH did not alter the conception rate.More Mo-supplemented animals failed to ovulate following prostaglandin induced synchronization in comparison with the other treatments, and by the 84th week a significantly greater number of Mo-supplemented animals (12/18) had become anoestrous compared with the other groups (2/30). Cu repletion of these anoestrous Mo animals for a period of 20 weeks did not result in resumption of normal oestrous cycles, but ovulation and oestrus were induced by progesterone and LHRH treatment. Results in the latter part of the study indicated that Mo caused superovulation.These data show that Mo supplementation delayed the onset of puberty, decreased the conception rate and caused anovulation and anoestrus in cattle without accompanying changes in Cu status or in live-weight gain. It is suggested that these effects of Mo are associated with a decreased release of luteinizing hormone that might be due to an altered ovarian steroid secretion.

Four non-lactating red deer hinds kept in natural light were each given orally 5 mg melatonin daily in the afternoon from 1 June to 5 October. The time difference between melatonin administration and sunset was 5.5-6 until the end of August, thereafter gradually decreasing to 3.5 h. Onset of oestrous cyclicity occurred in late August and early September, 2-8 weeks in advance of control hinds. A stag given 10 mg melatonin daily shed the antler velvet on 18 July, 4 weeks earlier than untreated stags, and started rutting behaviour in July-August, 2 months before the usual time.

Goat meat production is an expanding industry in Australia. However, there is limited data quantifying the levels of reproductive performance, particularly under extensively grazed rangeland conditions, which would inform interventions to improve performance. This review aimed to quantify the levels of reproduction, time and causes of reproductive wastage in goats. It considers the levels of fertility, fecundity, embryonic loss, fetal loss and post-natal survival reported under Australian conditions, and comparisons are made with international reports. Key management factors that may contribute to reproductive performance include breed, seasonality, nutritional conditions, and weather conditions at kidding. While goats are potentially prolific breeders, in Australia, the variation in weaning rate (kids/doe joined) among properties is large (51–165%), although the causes of this variation are not well defined. Generally, conception and kidding rates are high, although fetal loss associated with undernutrition is more likely in goats than sheep. As with sheep, perinatal losses are generally the largest source of wastage, with an average 20% kid mortality, but this level is influenced by litter size and appears to be higher under extensive rangeland systems. The causes of perinatal kid loss under Australian conditions are similar to those in sheep, with starvation–mismothering–exposure and dystocia or stillbirth the key causes. Studies are needed to accurately quantify the level and causes of reproductive wastage in commercial herds, including a range of management situations, to enable effective interventions to be developed.

Interactions between protein supply and the anabolic response to exogenous bovine (b) GH have been examined in two experiments using 28-35 kg lambs sustained entirely by intragastric infusion of volatile fatty acids (700 kJ/kg W 0.75 per day) into the rumen and the casein (600 mg (low protein; LP) or 1200 mg (high protein; HP)/kg W 0.75 per day) into the abomasum. Sheep received continuous i.v. infusions of bGH for 6 days in experiment 1 and for 18 days in experiment 2. Nitrogen balances were determined daily throughout both experiments and blood samples, from indwelling catheters, were assayed for GH, insulin-like growth factor-I (IGF-I), insulin and glucose. Infusion of bGH increased plasma GH concentration by five- to sixfold in all animals. There was an increase in N retention in both HP and LP animals over the first 2-3 days of GH administration. HP animals sustained higher N retentions (31%; P less than 0.05) throughout the GH administration but LP animals did not. In contrast, plasma IGF-I concentrations increased progressively over the first 72 to 96 h of GH administration in all sheep and thereafter remained significantly (P less than 0.05) elevated until termination of the GH infusion. In lambs which received both HP and LP infusion in experiment 1 the increase in IGF-I and LP infusions in experiment 1 the increase in IGF-I concentration by day 6 of GH administration was significantly (P less than 0.05) greater when they received the higher protein intake.(ABSTRACT TRUNCATED AT 250 WORDS)