Seasonality of ovulation and estrus, and the ram effect in poll dorset ewes

The effects of month on the proportion of Poll Dorset ewes expressing estrus and ovulating and on their ovulation rate when continually exposed to vasectomised rams and the effects of isolating the ewes from rams in winter/early spring were examined during 15 months in New South Wales, Australia. The percentage of ewes ovulating and their ovulation rate varied from 23% and 1.10 in November to an average of 99% and 1.85 in April and June, and the proportion of ewes expressing estrus followed a similar trend. Some ewes (6.8%) ovulated throughout the 15 months, and the average breeding season was 294 (SE = 6.1) days. Isolating ewes from rams in late winter/early spring significantly decreased the proportion of ewes ovulating from September to November, increased the proportion in December, but did not significantly alter ovulation rate. The variability in reproductive measures during spring offers scope for selection; with the ram effect, improvements in spring joining results from Dorset ewes are possible.     

Effects of boar pheromones,ram's wool and presence of bucks on ovarian activity in anovular ewes early in the breeding season

Dorset ram's wool applied to the muzzle of anovular ewes early in the breeding season stimulated 40–53% of the ewes to ovulate within 4 days. The active components of the pheromones produced by the boar, 5α-androst-16-ene-3-one and 3α-hydroxy-5α-androst-16-ene, failed to stimulate anovular ewes to ovulate early in the breeding season. In contrast, the male goat (buck) was as effective as the Dorset rams at stimulating anovular ewes to ovulate (57% v. 76%). The results suggest that rams and bucks produce a similar pheromone which will stimulate anovular ewes.     

Testosterone levels in Dorset and Romney rams and the effectiveness of these breeds in stimulating early onset of estrus in Romney ewes

Groups of Romney ewes were joined with either Dorset or Romney rams on December 24 1975 and further groups joined on January 30 1976. A control group was subjected to laparotomy and joined with Romney rams after first ovulation was observed. Matings were recorded daily in all groups. At weekly intervals rams were separated from ewes and bled every 10 minutes for one hour. The plasma was radioimmunoassayed for testosterone.Ewes run with rams showed their first estrus of the breeding season earlier than controls and their onset was more synchronised. The time of ram joining did not affect the time of first estrus but ewes joined with Dorsets showed their first estrus earlier than those with Romneys. Romney rams had significantly higher mean testosterone levels than Dorsets on 5 of the 11 weekly bleedings throughout summer. The testosterone level decreased significantly over the seven consecutive bleedings of the hourly sampling period in five weeks and a significant interaction between breed of ram and testosterone level of consecutive bleedings was observed in three weeks.The results show that testosterone levels in Dorset and Romney rams during summer do not reflect the effectiveness of the breeds in inducing the early onset of estrus in Romney ewes.     

The ovarian and hormonal response of the ewe to stimulation by the ram early in the breeding season

The introduction of Dorset rams to Romney ewes at the beginning of the breeding season (February 14 to March 1) stimulated 39% to 70% of the non-cycling ewes to ovulate. Most of the ewes that ovulated did so within 65 to 72 hours of ram introduction. The ovulations were preceded by LH peaks, the mean onset of which was 35.0±4.8 (SE) hours after ram introduction. The mean oestradiol-17β concentration per ewe ranged from 0.3 to 14.9 pg/ml plasma and there were large fluctuations among the samples collected every 3 hours. All ewes, irrespective of treatment, had similar mean concentrations of oestradiol-17β and ovarian follicular activity, and there were no changes in oestradiol-17β concentration that could be attributed to the presence of the rams.     

A definition of the breeding season of Pool Dorset ewes

The seasonality of oestrus and ovulation of 62 Poll Dorset ewes was examined over a period of 16 months commencing October, 1981. Laparoscopic observations showed that the majority of these ewes were anovular during the South Australian spring and early summer (September to December). The number of ewes with corpora lutea (93.6%) and the mean ovulation rate (1.62) reached a peak in June. Oestrus was stimulated in anovular ewes in late spring by the introduction of vasectomised rams. The mean ovulation rate at the teased ovulation was 1.68, although teased ewes did not exhibit oestrus at this ovulation.     

Corpus luteum function in ewes stimulated by rams

In late February Dorset rams were introduced (day = 0) to 40 mature Romney ewes that were observed by laparoscopy to be anovular. The ovaries of 20 of these ewes were examined by laparoscopy every second day while the remaining 20 ewes served as unoperated controls. Jugular blood samples were taken daily and plasma progesterone concentrations assayed to provide information on the functional status of any corpora lutea (CL) arising from ovulations stimulated by introduction of the rams. Eighty-five percent (-17/20) of the ewes that were repeatedly laparoscoped had ovulated within 4 days of ram introduction and premature regression of the CL had occurred between days 4 and 8 in 8 ewes and days 6 to 10 in 2 ewes. A second ovulation was observed after or during the premature regression of the first CL and this subsequent CL was maintained for the normal duration. The prematurely regressing CL produced a small peak in progesterone concentration on days 4 to 5 but the concentrations declined on days 6 to 7. In the unoperated ewes 50% (-10/20) appeared, from the progesterone profiles, to have ovulated by day 4 and half of these appeared to have premature CL regression. The interval from introduction of the ram to first oestrus was 23 days in ewes with premature regression of the CL and 19 days in ewes ovulating within 4 days but having no premature regression. From the results it was concluded that the premature regression of the CL is the cause of the delayed interval from ram introduction to first oestrus in Romney ewes and is a major factor contributing to the two peaks of oestrous activity observed after ram introduction.     

Reproductive potential and endocrinological responses of sheep kept under controlled lighting. II. Pituitary and gonadal responses of ewes and rams to a six-monthly light cycle

Forty entire ewes of mixed breeds were kept in environmentally-controlled rooms with a 6-monthly light cycle. Six mature spayed Border Leicester × Merino ewes and four mature intact Poll Dorset rams were kept under the same conditions.Over a period of 2 years (four light cycles) estimates were made of ovarian, testicular and pituitary activity in response to the artificial light regime. Non-pregnant ewes were bled twice weekly: peripheral plasma progesterone levels > 1 ng/ml were taken as indicative of ovarian activity. Testicular activity was estimated by weekly tests for peripheral plasma testosterone and scrotal sac volume. Pituitary activity was estimated monthly by the response to the injection (i.v.) of 75 μg gonadotrophin releasing hormone (GnRH) to rams and of 18.75, 37.5 or 75 μg to ewes, using peripheral plasma luteinising hormone (LH) estimations from the time of GnRH injection.Data for ovarian and testicular measurements were classed into categories according to week and for pituitary response to month of the light cycle.Cubic regression analyses were conducted on the percentage of ewes with progesterone levels > 1 ng/ml and on ram testosterone and scrotal measurements.Despite the irregularity of the curve for the light cycle, the ovarian and testicular responses of rams and ewes followed an alternating curve with peaks and troughs of activity separated by approximately 13 weeks in the 26-week cycle. The peak of ovarian activity occurred during the long daylength period which followed a 22-week period of decreasing daylength and was preceded by 1 month by peak ram testosterone and scrotal sac volume.The pattern of pituitary response was related to that of the actual light cycle and the data were subjected to time-lag regression. This econometrical technique revealed that there was a delay in pituitary response to daylength changes of 2 months for rams, and between 2 and 3 months for the spayed ewes. The peak pituitary response to the GnRH test occurred one month earlier for rams than for the spayed ewes, and coincided with the corresponding troughs of gonadal activity of each sex.The results showed that the breeding season of sheep can be compressed into 6 months and that the pattern of pituitary response follows the daylength pattern more closely than do measurements of gonadal activity. Peak reproductive activity in rams, as measured by pituitary and gonadal activity, precedes that of ewes by approximately 1 month.     

Scrotal circumference measurements in purebred Dorset, Hampshire and Suffolk lamb and yearling rams

Purebred Suffolk, Hampshire and Dorset lamb and yearling rams (n=753), underwent performance testing from 1986 to 1989. Scrotal circumference, birth date and entry weight were recorded for each ram entering the test station. Mean age in days at entry, weight (lbs), and scrotal circumference (SC; cm) were greatest for the Hampshire rams. For all rams combined (Dorset, Hampshire and Suffolk), the mean SC by month of age revealed rapid growth from 2 to 6 mo, with a 3- to 6-mo mean SC significantly (P0.05) for mean SC measurement and a less rapid increase in SC diameter. Between 12 and 13 mo a significant increase (P相似文献   

Sperm output and hormone concentrations in Finn and Dorset rams exposed to long- and short-day lighting

Seasonal changes in photoperiod have a substantial effect on sexual behavior and reproduction in rams. Little information is available on sperm output from high libido versus average libido rams subjected to intensive semen collection while being exposed to controlled short versus long photoperiods. Six Finn and six Dorset rams were compared in a reversal design, which allowed rams of both breeds to be exposed to 8 h versus 16 h of light. During each of two 84-d periods rams were subjected twice to an initial depletion of epididymal sperm reserves by collecting up to 26 ejaculates of semen in 3 d, followed by up to 10 ejaculates per day, 1, 3, 5, and 7 d after the initial depletion. A total of 2673 semen samples were collected. Nearly twice as many ejaculates (63.6% of the total) were obtained from Finn rams as from Dorset rams during both the initial and subsequent 3-d sperm depletion periods. This difference in libido was associated with obtaining 33.6 +/- 3.1 x 10(9) sperm from Finn rams versus 10.0 +/- 2.2 x 10(9) sperm from Dorset rams during the initial depletion period (P<0.05). Changes in photoperiod did not affect sperm output (P>0.05) in Finn rams, but may have affected Dorset rams. With 16 h of light, prolactin was significantly (P<0.05) increased in both breeds, particularly in Finn rams. Testosterone in both breeds followed an endogenous rhythm, not affected by the change in controlled photoperiods.     

Use of gonadotropin releasing hormone to improve reproductive responses of ewes introduced to rams during seasonal anestrus

Three experiments were conducted on anestrous ewes of Suffolk, Dorset, and Katahdin breeding to examine the potential value of GnRH to improve ovulation and pregnancy in response to introduction of rams. In Experiment 1, treatment with GnRH 2 d after treatment with progesterone (P₄; 25 mg i.m.) at introduction of rams was compared to treatment with P₄ alone at the time of introduction of rams. Treatment with GnRH did not increase percentages of ewes with a corpus luteum (CL) 14 d after introduction of rams, pregnant 32 d after treatment with PGF₂α 14 d after introduction of rams, or percent of treated ewes lambing to all services. In Experiment 2, treatments with GnRH on day 2, 7, or both after introduction of rams were compared. Treatments did not differ in mean estrous response, percentages of ewes with a detectable CL or number of CL present on day 11, or mean pregnancy and lambing rates. Therefore, neither one nor two injections of GnRH at these times appeared to be effective to induce anestrous ewes to breed. In Experiment 3, treatments compared included GnRH 4 d before introduction of rams, GnRH 4 d before and 1 d after introduction of rams, ram introduction alone, and treatment with P₄ (25 mg i.m.) at the time of introduction of rams. Percentages of ewes with concentrations of P₄ greater than 1 ng/mL (indicating formation of CL had occurred) 7 d after ram introduction tended to be greater (P < 0.07) in ewes treated with GnRH or P₄ than in control ewes treated with ram introduction alone. However, there was no difference in P₄ concentrations between groups by day 11 or 12 after introduction of rams. Estrous response rates and percentages of ewes pregnant 95 d after PGF₂α was administered (on day 12 after introduction of rams) tended to be greater (P = 0.08 and 0.06, respectively) in ewes treated with GnRH or P₄ than in ewes exposed to rams only. There was no difference in response variables between ewes treated with GnRH 4 d before introduction of rams and ewes treated with GnRH 4 d before and 1 d after introduction of rams. In conclusion, treatment with GnRH 4 d before ram introduction showed promise as an alternative to treatment with P₄ to improve the ovulatory response and reproductive performance of ewes introduced to rams during seasonal anestrus.     

Effects of recent sexual experience and melatonin treatment of rams on plasma testosterone concentration, sexual behaviour and ability to induce ovulation in seasonally anoestrous ewes

The aim of this study was to determine whether advancing the seasonal changes associated with rams by treatment with exogenous melatonin and allowing the rams previous sexual experience would increase the proportion of anoestrous ewes ovulating in early July. North Country Mule ewes (n = 225) were grouped by live body weight and body condition score and allocated randomly to the following treatments: (i) isolated from rams (control; n = 25); (ii) introduced to rams (treatment 2); (iii) introduced to rams that had mated with ewes during the previous 2 days (treatment 3); (iv) introduced to rams implanted with melatonin (treatment 4); and (v) introduced to rams that were implanted with melatonin and had mated with ewes during the previous 2 days (treatment 5). Treatments 2-5 were replicated (2 x 25 ewes) and two rams were introduced to each replicate group. Introductions began on 4 July and were completed by 11 July. The rams were withdrawn from the ewes after 8 days. Melatonin was administered as a subcutaneous implant (Regulin((R))) on 22 May and again on 20 June. Blood samples were taken from all rams to determine plasma melatonin and testosterone concentrations (19 samples in 6 h). The behaviour of the sheep was videotaped continuously during the first 3 h after the ram was introduced. Ovulation was detected by an increase in plasma progesterone concentrations from < 0.5 ng ml(-1) to > 0.5 ng ml(-1). Mean +/- SE plasma melatonin concentrations were 649.7 +/- 281.4 and 18.3 +/- 2.4 pg ml(-1) in rams with and without melatonin implants, respectively (P < 0.001). Melatonin implants also increased plasma testosterone concentrations from 4.30 +/- 1.88 to 10.10 +/- 1.10 ng ml(-1) (P < 0.01), the libido of the rams and the proportion of ewes that ovulated in response to the rams (43 and 56% (treatments 4 and 5) versus 24% (treatments 2 and 3)). In conclusion, implanting rams with melatonin before introducing them to seasonally anoestrous ewes increases the proportion of ewes that ovulate in response to introduction of a ram, but previous sexual experience of rams appears to have little or no effect.     

Importance of behavioural stimuli in ram-induced ovulation in seasonally anovular Corriedale ewes

Three groups of about 65 seasonally anovular Corriedale ewes were penned and exposed to rams on November 4, 1989. A fourth group (n=64) was maintained in a 3-ha paddock and also exposed to rams on the same date. The sexual behaviour exhibited by rams in contact with penned ewes was recorded during nine simultaneous observation sessions lasting 2 h each.

Five days after ram introduction, incidence of ovulation and ovulation rate were higher (P < 0.01) in adult than in 1.5-year-old ewes. Among penned adult ewes, a greater (P < 0.05) incidence of ovulation was recorded in ewes maintained in contact with rams and oestrous ewes (95.8%) than in ewes exposed to either rams with or without recent experience with oestrous ewes (68.7 and 57.1%, respectively). The fourth group, exposed to rams in field conditions, exhibited a lower (P < 0.05) incidence of ovulation (31.9%) than any other group. No differences among treatments were detected in 1.5-year-old ewes. The incidence of ovulation was associated (r=0.99, P<0.05) with the sexual behaviour displayed by the rams.

It was concluded that the sexual behaviour of the rams plays an important role in ram-induced ovulation and that the continuous presence of oestrous ewes is necessary for the maximum efficacy of the technique in Corriedale ewes.     

Ram novelty and the duration of ram exposure affects the distribution of mating in ewes exposed to rams during the transition into the breeding season

This study compared the affect of short-term and continuous exposure to rams during the transition between anoestrus and the breeding season on the distribution of mating and subsequent lambing. Further, within ewes continuously exposed to rams we investigated the effect of replacing these rams every 17 days with 'novel' rams. During August (late anoestrus, Northern Hemisphere), multiparous, North of England mule ewes were allocated to one of four groups: SVR ewes were exposed to vasectomised rams for 24h on Day 0 (short term; n=109), RVR ewes were exposed to vasectomised rams for 24h on Days 0, 17 and 34 (short term; n=113); PVR ewes were exposed to vasectomised rams on Day 0 and remained with the same rams for the duration of the pre-mating period (continuous; n=104); NVR ewes were continuously exposed to vasectomised rams from Day 0 with the rams replaced with 'novel' rams every 17 days (continuous; n=113). Blood samples were collected from a subset of ewes (n=22 per group) to monitor progesterone. On Day 50, harnessed, entire rams were introduced for mating and raddle marks recorded daily for the first 17 days. The median date of mating occurred 1 day earlier in NVR ewes than PVR ewes (P<0.05). A synchrony score calculated from the blood sampled ewes showed that the distribution of mating was more synchronised in PVR and NVR ewes than SVR and RVR ewes (P<0.001). PVR and NVR ewes had an earlier onset of cyclic activity than RVR ewes (P<0.01). However, only NVR ewes differed from SVR ewes in this variable (P<0.05). Within ewes lambing to first service, the median date of lambing of PVR, NVR and SVR ewes occurred at least 2 days earlier than RVR ewes (at least P<0.05). Further, PVR and NVR ewes had a more compact distribution of lambing than SVR and RVR ewes (P<0.05) and lambing was more compact in NVR ewes than PVR ewes (P<0.05). In conclusion, ewes in continuous contact with rams prior to mating had a more synchronised distribution of mating and lambing than ewes given only short-term exposure to rams. This distribution of mating in continuous ram exposed ewes can be further enhanced by periodic exposure to novel rams.     

Estimates of early embryonic loss in ewes mated to rams selected for high and low prolificacy

Two closed lines of sheep selected for high and low prolificacy were established in 1969. Rams within each line were selected on the basis of their dams' lambing records. Foundation ewes were assigned at random to selected rams, and no ewe selection was practiced until replacement yearlings were selected for mating. Selection of the rams used to mate the foundation ewes resulted in more lambs born per 100 ewes exposed to the ram (P<.10) and more lambs born per 100 ewes lambing from the high line rams (P<.05).Seven rams from each line were then used to estimate fertilization rate and embryonic survival rate when mated to an unrelated group of ewes. There was no difference in ovulation rate or fertilization rate of ewes mated to low and high line rams. Percent eggs recovered per CL was 80 and 92 (P<.01) for low and high line rams, respectively. At 35 days 82 and 86% of the ewes were pregnant, and 84 and 93% of the CL were represented by embryos in the pregnant ewes mated to low and high lines, respectively. Estimated embryonic survival rates were 81 and 89% in ewes mated to low and high line rams, respectively.     

Ram effect: adult rams induce a greater reproductive response in anestrous ewes than yearling rams

The introduction of rams to previously isolated anestrous ewes ensures induction of ovulation and estrus in part of the flock, and allows for the potential to conceive. However, there is little known about the desirable characteristics of the rams used to induce these behavioral and physiological responses. Adult rams may be more effective than young rams in induction of these responses. The primary aim of the present study was to compare the response in ewes stimulated by adult or yearling rams. During the non-breeding season, two groups of 121 ewes were stimulated with adult (AR) or yearling (YR) rams. When adult rams were used, significantly more ewes had ovulations (78.5 compared with 61.1%) and came into estrus (47.9 compared with 35.5%). There were more corpora lutea per ewe exposed to rams (0.95+/-0.59 compared with 0.65+/-0.51) and per ewe that had ovulations (1.18+/-0.41 compared with 1.06+/-0.25) and a greater conception rate (58.6 compared with 20.9%) as a result. Subsequently, to determine what signals led to the greater response to adult rams, the courtship behavior of adult and yearling rams toward anestrous ewes was compared in 46 pen tests. There were no significant differences in the frequency of any of the recorded courtship behaviors (anogenital sniffing: 21.9+/-3.4 versus 25.7+/-3.2; lateral approaches: 7.1+/-1.5 compared with 9.9+/-2.9; flehmen: 2.1+/-0.4 compared with 2.2+/-0.4; mount attempts: 0.1+/-0.1 compared with 0.1+/-0.1, for AR and YR, respectively), latency to the onset of courtship behavior (13.1+/-7.0 compared with 17.3+/-6.2s) or the time engaged in courtship behavior (173.1+/-24.6 compared with 199.0+/-26.5s). The difference in the signals produced by adult and yearling rams skin glands was assessed by stimulating ewes with masks containing wool from adult (n=45) or yearling (n=48) rams. More ewes had ovulations (24/45 compared with 11/48) and came into estrus (21/45 compared with 10/48) when wool from adult rams was used. As in Experiment 1, pregnancy and conception rates were greater when adult rams were used, another trial was designed to determine if there were differences in mating and mounting frequency between adult and yearling rams. Seven adult and six yearling rams were subjected to three pen tests each with three estrual ewes. Adult rams mounted more (21.7+/-4.5 compared with 9.8+/-0.7) and tended to ejaculate more frequently (2.9+/-0.5 compared with 1.8+/-0.4) than yearling rams. It is concluded that adult rams induce a greater reproductive response in anestrous ewes than yearling rams, inducing a greater ovulation percentage and estrous response in ewes, resulting in greater ovulation numbers, pregnancy and conception rates. This greater stimulation is, in part, explained by differences in the signals provided in the wool (presumably odors) produced by adult rams. The lesser percentage of pregnancies obtained when yearling rams are used may be explained by differences in mounting behaviors and ejaculation frequency.     

Prior exposure of maiden ewes to rams enhances their behavioural interactions with rams but is not a pre-requisite to their endocrine response to the ram effect

In this study, we tested whether prior experience with rams would modify the behavioural and endocrine responses of maiden ewes to rams. During mid-anoestrus, sexually na?ve, maiden ewes were exposed to rams for 7 days (ram experienced, RE; n=61) or isolated from rams (ram na?ve, RN; n=63). All ewes were subsequently isolated from rams. In Experiment 1, RE (n=55) and RN (n=57) ewes were introduced to rams during late anoestrus. RE ewes had more total and positive interactions with rams than RN ewes (P<0.001). RE ewes showed more ram seeking behaviour and spent more time in proximity of rams than RN ewes (at least; P<0.05). In Experiment 2, RE (n=6) and RN (n=6) ewes were introduced to rams midway through a frequent blood sampling regime in late anoestrus. Ram introduction stimulated an increase in LH pulse frequency and basal LH in both RE and RN ewes (at least P<0.05). RE ewes had an increase in mean LH concentrations (P<0.01) that failed to reach significance in RN ewes (P<0.1). There was no significant effect of prior experience with rams on LH pulse frequency, amplitude or whether ewes had an LH surge. In conclusion, prior experience with rams is important in developing appropriate ewe-ram interactions but is not a pre-requisite to the endocrine response to the ram effect.     

Sheep breeding schemes utilising artificial insemination; large-scale simulation with a complex breeding goal

Alternative Norwegian sheep breeding schemes were evaluated by stochastic simulation of a breeding population with about 120 000 ewes, considering the gain for an aggregate genotype including nine traits and also the rate of inbreeding. The schemes were: a scheme where both young unproven rams (test rams) and proven rams (elite rams) are used in artificial insemination (AI scheme), a scheme with test rams in natural mating in ram circles and elite rams (from one and a half years of age) in AI across all flocks in the country (NMAI2 scheme), a scheme where, in addition to testing rams, the youngest elite rams (one and a half years of age) are also used in natural mating in ram circles, while older elite rams are used in AI (NMAI1 scheme), and a scheme, acting as a control, where both test and elite rams are used in natural mating (NM scheme). Within the NMAI- and AI-schemes, experimentation was performed for percent ewes inseminated to elite rams v. test rams (EM%), numbers of ewes inseminated per elite ram (EAIn), and numbers of ewes mated per test ram by natural service (TNMn) or by AI (TAIn), respectively. With a restriction on the rate of inbreeding (⩽0.8% per generation), the AI scheme gave similar gain to the NMAI2 scheme (and about 40% more than did the NM scheme). Less gain was generated by the NMAI1 scheme, but it was still considerably more than for the NM scheme (about 25%). In the AI scheme, relatively few ewes (200/300) should be inseminated to each test/elite ram, and a low EM% should be chosen (10%). In the NMAI schemes, TNMn should be relatively high (40 to 50), combined with average and somewhat larger than average EAIn (NMAI2: 700 ewes, NMAI1: 900 ewes), and EM% medium (30%).     

Sexual maturation of ewes raised without ram exposure in a controlled lighting environment

Finn x Dorset ewe lambs (n = 70) born in the spring (March 28 to April 6) from two successive lambing seasons were evaluated for age at first ovulation in the absence of mature rams. Ewe lambs were born in a controlled, short light (8L:16D) photoperiod or in ambient light (13L:11D). At about 10 to 11 wk of age, ewe lambs were allocated to a short (8L:16D) or long (16L:8D) light environment. Plasma progesterone (P(4)) concentrations were measured as an index of first ovulation. First exposure of ewes to sexually mature rams was in November. Most ewe lambs (77%) ovulated before ram exposure. More lambs (P < 0.025) born in ambient light and raised in short light reached puberty with typical cycles of plasma progesterone compared to other treatments. Long days tended to retard the onset of puberty. Although pregnancy rate did not differ across light treatments, more ewes became pregnant from the ambient-light born and short-light raised treatment. Photoperiod is an important factor affecting the onset of sexual maturation and genesis of normal luteal progesterone secretion in the ewe lamb.     

Combination of the ram effect with PGF2α estrous synchronization treatments in ewes during the breeding season

The role of the ram effect on the reproductive performance of ewes that have initiated estrous cycles following lambing in combination with synchronization of estrus using PGF(2α) was examined. A total of 1264 Corriedale × Merino ewes in the breeding season (March-April) were allocated to one of three treatments. The control group (PG2) of ewes (n=415) were in permanent direct contact with vasectomized rams throughout the experiment from 60 d prior to the administration of the first luteolytic dose of PGF(2α) which was followed by a second dose 13 d later (Day 0 of the experiment). Ewes assigned to the other two treatments remained isolated from rams until Day 0. In the second treatment, ewes (PG2RE; n=445) were administered PGF(2α) in the same manner and were joined with vasectomized rams at Day 0. Ewes allocated to the third treatment (PGRE; n=404) did not receive the second dose of PGF(2α) but were introduced to vasectomized rams on Day 0. Sexual receptivity, as indicated by tail-head marking, was recorded until d 11. More PG2RE ewes (407/445; 92%) were observed in estrus by Day 11 than occurred for PG2 ewes (353/415; 85%; P=0.003). The accumulated frequency of PG2RE ewes in estrus was greater than for PG2 ewes for each period from Day 3 (P<0.001) to Day 11 (P<0.01). The onset of estrus was earlier in PG2RE ewes (2.98±0.07 d) than for PG2 ewes (3.31±0.07 d; P<0.0001). In contrast, the total frequency of PGRE ewes observed in estrus by Day 11 (356/404; 88%) was similar to that observed for PG2 ewes. However, the trajectory of the accumulated frequency of the incidence of estrus was less for the PGRE ewes initially, particularly during the period of Days 3-6 of observation (P<0.0001). Consequently, onset of estrus was earlier in PG2 ewes (3.31±0.07 d) than for PGRE ewes (5.30±0.11 d; P<0.0001). It was concluded that the introduction of vasectomized rams simultaneously with the second administration of PGF(2α) advanced the onset of estrus and increased the number of ewes that responded. The introduction of rams 13 d after a single dose of PGF(2α) did not substitute for the second administration of PGF(2α).     

The number of spermatozoa required by naturally mated ewes and the ability of rams to meet these requirements

The fertility of naturally mated ewes was compared with the number of spermatozoa deposited, and the number of times they were mated. The number of spermatozoa received was estimated from ejaculates flushed directly from the vagina of naturally mated ewes.In one experiment, maximum fertility was achieved with as few as 140 × 10⁶ spermatozoa. The percentage of pregnant ewes was similar in ewes mated once or more than once (68.4% vs. 72.5%). Similar results were obtained in one test of a further experiment but in a second test fertility was higher in ewes that were mated more than once. If this effect was due to the extra spermatozoa received, then ewes required 500 × 10⁶ spermatozoa to achieve maximum fertility. Half of the ewes were mated at their first oestrus after treatment with progestagens in the second experiment. The fertility of these ewes was similar to that of the remaining ewes, which were mated at natural oestrus.The mean number of spermatozoa ejaculated by individual rams varied from 140 × 10⁶ to 1050 × 10⁶, following depletion of the epididymal reserves of spermatozoa. The rams ejaculated an average of 9.1 × 10⁶ spermatozoa per gram of testis per day in the first experiment. The rams mated an average of 10.9 times per day in the first experiment, 6.9 and 6.1 times per day, respectively, for the first and second tests in the second experiment. The number of times that rams mated was highly correlated with the number of ewes with which they mated in the second experiment.