Influence of the presence of a mature female on puberty attainment in gilts

At 90 days of age, 40 Large White gilts were assigned to one of two treatments. At 155 days, a mature female which was left intact (Treatment I) or ovariectomized (Treatment O) was placed in each pen of five experimental gilts. From 180 days, estrus was checked daily with the back pressure test, and the occurrence of ovulation was detected by measuring the concentration of plasma progesterone at weekly intervals. From 240 days, a mature boar was introduced, for 5 minutes daily, into each pen during estrus detection. Gilts were slaughtered within 12 days after ovulation or at 270 days of age if they were not cyclic earlier. The percentage of gilts reaching puberty before 225 days of age was significantly higher in Treatment I (7 19 ) than in Treatment O (0 19 ) even though the average age at puberty was similar (I, 231 +/- 24 days; O, 243 +/- 12 days; mean +/- SD). Age at puberty and the number of days between mature female introduction and puberty differred significantly between the pens of gilts in Treatment O but not in Treatment I. Ovarian weights, ovulation rate and percentage of gilts with silent estrus were similar in the two treatments. Thus, the occurrence of pubertal estrus may be influenced by contact with an older, cyclic female or with other contemporary females raised in the same pen.     

Impact of boar exposure on puberty attainment and breeding outcomes in gilts

We examined the most effective method of boar exposure for the attainment of puberty in 89 gilts. At 160 days of age, we allocated gilts to daily direct contact with a vasectomized boar after movement of pen groups of gilts to a detection-mating area (DGB: n = 30); daily direct contact with boars in the gilt home pens (DBG: n = 31); or daily fenceline contact between boars and gilts housed in individual gilt stalls (FBG: n = 28). DGB gilts were younger (P < or = 0.05) than FBG gilts at puberty. Direct boar contact reduced the interval from initial boar contact to puberty in DGB and DBG gilts, compared to fenceline contact in FBG gilts (P < 0.05). There was no difference (P > or = 0.05) between treatment for pubertal weight, backfat, lifetime growth rate, or duration of first pubertal estrus. Backfat depth and leptin concentration at 160 days of age were positively correlated (P < or = 0.05). We detected no relationships between leptin or IGF-1 concentration at 160 days of age and the interval from initial exposure to a vasectomized boar to puberty (P > 0.05). Based on objective criteria, fenceline contact with a boar (BC) during artificial insemination improved the quality of artificial insemination compared to no boar contact (NC) (P < 0.05).     

The involvement of boar submaxillary salivary gland secretions in boar-induced precocious puberty attainment in the gilt

The involvement of secretions from boar submaxillary salivary glands in mediating the induction of precocious puberty in the gilt was investigated as follows. Forty-eight Large White × (Large White × Landrace) prepubertal gilts from 12 litters were randomly allocated within litters by weight, to four treatment groups of six, in two replicates, at 145 days of age. Treatments commencing at a mean group age of 165 days, were: (1) control (no boar exposure); (2) gilts exposed to a mature sialectomised boar (submaxillary salivary glands were removed at 9 weeks of age); (3) gilts exposed to a mature sham-operated boar; (4) gilts exposed to a mature unoperated boar.Boar exposure occurred for 30 min per day for 75 days, or until pubertal oestrus was observed. Gilts showing pubertal oestrus were removed and slaughtered. Ovaries were examined to confirm reproductive status. Gilts failing to exhibit oestrus by 240 days of age were slaughtered and nominally ascribed a pubertal age of 245 days. Age at puberty was significantly earlier in all three boar-exposed treatments than in the control treatment (P<0.05 for treatments 2 and 3, P<0.001 for treatment 4; median ages at puberty being 227.0, 203.5 , 202.0 and 179.0 days for treatments 1 to 4 respectively). No frothy saliva was ever produced by the sialectomised boar, and chromatographic analysis of saliva produced by the sham-operated boar during mating revealed very low levels of 16-androstene pheromones, while levels in the unoperated boar's saliva were normal. These results provide further evidence for an important role of boar salivary pheromones in the induction of precocious puberty attainment in the gilt.     

The effect of modified eros centre, outdoor raising or conventional group housing on breeding gilts and its effects on reproductive performance over four parities

The present study was conducted in a large Croatian "built up unit". The objective of the study was to determine if an indoor modified eros centre (MEC) compared to indoor or outdoor group housing of gilts, influenced the onset of puberty of gilts and the reproductive performance of the evaluated females (n = 783) over four parities. The gilts were from the same nucleus herd. Gilts of same age (140-150 days of age), body condition (body condition score of 3-4) and similar genetics (four-way cross females), during the same season (January to April 1999), were randomly divided at arrival into three groups and treated as follows:MEC gilts (n = 279): These were placed into indoor MEC pens in groups of 8-10. The gilts had continuous fenceline contact to boars (one boar to two groups of gilts, boars were changed daily) and to shortly weaned oestrous sows. Gilts were regrouped and dislocated at 10-day intervals. Outdoor gilts (n = 263): These were kept in groups of 8-10 on a large pasture (80-100 m2 per group). The animals had fenceline contact to mature boar for 5-10 min daily. Control indoor gilts (n = 241): These were housed indoors in large pens in groups of 8-10. The animals had fenceline contact to mature boars for 5-10 min daily. Each outdoor group had an insulated hut with straw bedding. All gilts were fed ad libitum with the same commercial diet. Housing gilts in MEC resulted in earlier (P < 0.001) onset of estrus (MEC: 174.8 +/- 2.4 days, indoor group housing: 207.6 +/- 4.1 days, outdoor group housing: 187.4 +/- 2.1 days) and lower (P < 0.001) farrowing rate to first service (MEC: 70.97%, indoor group housing: 89.73%, outdoor group housing: 89.62%). Farrowing rate of regularly returning MEC gilts to second service was 95.00%. First total-born litter size, first liveborn litter size, first wean-to-estrus interval (WEI), percent of sows bred after first weaning, second total-born litter size, second liveborn litter size, average third and fourth total-born and liveborn litter size, number of sows having four litters, number of litters per sow, total number of pigs per sow, total number of liveborn pigs per sow showed no significant differences between the groups. More (P < 0.05) sows were culled in outdoor group. Compared to MEC and outdoor housing, indoor housed sows suffered higher (P < 0.05) percentage of anoestrus.     

Effect of lighting regimen,rearing in isolation and olfactory bulbectomy on growth and puberty in Yorkshire gilts

This study was designed to determine the effects of isolation or group rearing, total darkness or constant light, and olfactory bulbectomy on growth and onset of puberty in Yorkshire gilts. Forty-eight gilts, 90 days old, were assigned randomly to the following treatments: rearing in isolation with constant darkness, IS-CD; isolation with constant light, IS-CL; isolation with natural summer daylength, IS-NL; group rearing with natural daylength, GR-NL. They were reared in these environments to 245 days of age, without exposure to a boar. Twelve gilts, ～ 100 days old, were olfactory-bulbectomized (OB) and ten sham-operated (SC) littermates served as controls. They were reared in natural daylength in their respective groups, without exposure to a boar. Average weekly gains were similar among all treatment and control groups, ranging from 4.5 to 4.8 kg. Percentages of gilts in groups IS-CD, IS-CL, IS-NL and GR-NL that exhibited pubertal estrus by 245 days of age were 50, 50, 50 and 75, respectively (P>0.05), and the corresponding average ages of them at puberty were 208, 220, 213 and 205 days (P>0.05). In OB gilts, the percentage of them cycling at 270 days (33) was less (P<0.05) than that of SC (80). Sequential profiles of peripheral blood serum concentrations of progesterone confirmed normal estrous cycles after pubertal estrus of individual gilts among all treatment and control groups. These results indicate that rearing of gilts in isolation with either total darkness or constant light has no significant detrimental effect on their growth, age at onset of pubertal estruc and subsequent estrous cycles. Olfactory bulbectomy during the prepubertal period, however, delays onset of puberty but does not result in permanent loss of ovarian function.     

Effects of exposure to an estrual female on the attainment of puberty in gilts

A total of 304 prepubertal gilts were randomly allocated to 4 treatment groups across 10 replications for a 50 d treatment period beginning at 170 d of age. The 4 treatment groups consisted of: 1) Gilts that were continuously exposed to one of a group of older, ovariectomized females that had been treated with 2 mg/ml estradiol benzoate to stimulate estrus (SE); 2) Gilts that were continuously exposed to an older, anestrous, ovariectomized female (OVX); 3) Gilts that were exposed to a mature boar for 15 min/d (BE); 4) Gilts that were isolated from any direct physical contact with other pigs (C). A gilt was considered to have attained puberty when she exhibited a standing reflex when mounted by the boar (BE group only) or to pressure applied manually to the back or had plasma progesterone concentrations > 2 ng/ml for 2 consecutive weeks. Data were analyzed as a randomized complete block design with treatment and replication in the model. A higher percentage of gilts attained puberty in the BE group than in the 3 other groups (52 vs 26, 30 and 32%, BE vs SE, OVX and C, respectively; P = 0.002). Gilts exposed to an estrual female or a mature boar attained puberty sooner after treatment was initiated than gilts in other treatment groups (12.6 and 17.8 vs 26.7 and 24.1 d, SE and BE vs OVX and C, respectively; P = 0.0003). Of the gilts attaining puberty during the experimental period, the highest percentage of gilts exhibited estrus within 10 d of treatment in the SE group (55.0 vs 26.1, 37.8 and 16.7%, BE vs SE, OVX and C, respectively; P = 0.05). Age at puberty was also lower SE or BE than OVX or C groups (176.3 and 181.0 vs 189.4 and 188.1 d, respectively; P = 0.0001). Weight at puberty was unaffected by treatment. These results suggest that exposure to an estrual female was effective in stimulating peripubertal females to express estrus, thus reducing the age at puberty. Boar exposure had a stimulatory effect not only at the initiation of exposure but throughout the experimental period, resulting in a higher percentage of gilts attaining puberty.     

A note on the effects of contact frequency and time of day of boar exposure on the efficacy of the boar effect

Sixty-four Large White/Landrace crossbred gilts were used in this study, 16 gilts being allocated to each of four treatments to compare the effects on puberty attainment of exposure to boar contact either 0, 1 or 2 times daily. The once-daily exposure occurred in either the morning or the afternoon (AM vs. PM). Treatments were of 20-min duration starting at a mean gilt age of 160 days and continuing for 60 days. Boar exposure significantly increased the proportion of gilts attaining puberty within 60 days of the commencement of treatments (P < 0.05) compared with gilts not receiving boar contact. Gilts receiving boar exposure twice daily attained puberty significantly earlier than did gilts in the two treatment groups (AM and PM, respectively) given a single daily boar exposure period (mean gilt ages at puberty 176.4 vs. 192.7 and 189.2 days of age, respectively, P < 0.05). It is concluded that (a) twice-daily boar contact enhances the efficacy of the boar effect in gilts above that seen with a single daily boar exposure period and (b) this enhanced response of the gilt is due to the frequency of boar contact and not to the time of day at which the contact occurs.     

Attainment of puberty in female pigs: Clinical appearance and patterns of progesterone,oestradiol-17β and LH

The object of the study was to investigate the clinical and endocrine patterns of progesterone, oestradiol-17β and LH during the peripubertal period in female pigs. Crossbred gilts were penned in groups at an age of 10–12 weeks and boars were kept in adjacent pens during the entire experimental period. Daily oestrous checks started at 4.5 months of age and the gilts were slaughtered after their third heat. At the age of 4.5–5 months a permanent catheter was inserted in the cephalic vein and blood samples were collected from the gilts once daily until either the first or second oestrus. In three gilts hourly blood samples were taken during their first and second oestrus, beginning at early pro-oestrus.The gilts showed their first oestrus at the average age of 183 days. No corpora lutea from earlier ovulations were observed in gilts laparoscoped after their first detected oestrus. During the 30-day period before first oestrus the mean daily progesterone levels varied between 32 and 329 pmol/l. The average levels of oestradiol-17β varied between 15.6 and 30.8 pmol/l. There was no tendency for the oestradiol-17β level to rise before onset of first pro-oestrus. The average levels of LH varied between 0.15 and 0.94 μg/l. The statistical analyses revealed no significant relationship between the level of the hormones studied and onset of first oestrus. The mean progesterone levels during the first and second oestrous cycles were almost identical, however. Oestradiol-17β increased gradually during pro-oestrus, reaching maximum levels before onset of oestrus and thereafter decreasing sharply to values around 30 pmol/l. The oestradiol-17β levels were higher at the second than at the first pro-oestrous period. The concentrations of plasma LH rose sharply with declining plasma levels of oestradiol-17β. The duration of elevated plasma LH levels (> 1 μg/l) was, on average, 26 h and the LH levels were higher during the first oestrus than during the second oestrus. The first rise in progesterone was observed 11–29 h after the LH levels had decreased to concentrations below 1 μg/l.     

Effect of social conditions during rearing on mating behaviour of gilts

The mating behaviour of 28 gilts was studied. The gilts were reared under two different social conditions known to affect both their puberty attainment and reproductive parameters during early pregnancy. The different social conditions were applied from an average age of 137 days onwards. Ten gilts were housed individually, having neither tactile nor visual contact with other pigs. The remaining gilts (n=18) were housed pairwise, having additional contact with gilts in adjacent pens and daily boar contact from 180 days of age onwards. At third oestrus, the gilts were artificially inseminated and subsequently introduced to one of three vasectomized boars for a period of 20 min. The gilts were slaughtered 10±1 days after insemination.

The mating behaviour varied considerably between individual gilts, partly because of differences in mating behaviour between the two groups of gilts. More (P<0.05) individually housed gilts showed a standing response latency upon introduction of the boar. During this latency period, the individually housed gilts initiated contact with the boar. Once the standing response was elicited, mating behaviour was similar in gilts of both social groups. One individually housed gilt did not show a standing response and consequently was not mated. The mating behaviour of the boars did not differ for the gilts of the two social conditions.

It was concluded that the social conditions of gilts during rearing affected their introductory sexual behaviour. The relationship with reproductive performance during early pregnancy is discussed.     

Effect of sexual stimulation on concentrations of 5α-androstenone and testosterone in the peripheral plasma of boars reared individually

Six Yorkshire boars were reared from 107 days of age in individual pens. No female pigs were housed in the same building. When the boars were 200 days old, sows in oestrus were introduced to the pens of five boars and remained with the boars for 2 days. No oestrous sow was introduced to the pen with the sixth boar. Plasma 5α-androstenone and testosterone concentrations were low between 107 and 200 days of age in all boars. The maximum mean concentrations of these two steroids during this period were 6.18 ± 0.72 and 3.04 ± 1.02 ng/ml, respectively. Plasma 5α-androstenone concentrations increased with advancing age (P < 0.01). A similar trend was not seen for plasma testosterone concentrations. Plasma concentrations of 5α-androstenone and testosterone increased by 247 ± 27% (P < 0.02) and 1212 ± 204% (P < 0.001), respectively, in the samples drawn 24 h after the introduction of the sexually receptive sows. The maximal mean concentrations recorded following sexual stimulation were 12.90 ± 1.80 and 17.51 ± 1.96 ng/ml for 5α-androstenone and testosterone, respectively. The control boar also showed increases in plasma 5α-androstenone (221%) and testosterone (751%) concentrations in the same period, probably in response to auditory and olfactory stimuli originating in the pens nearby with introduced oestrous sows.     

The effects of zearalenone on reproduction in swine. II. The effect on puberty attainment and postweaning rebreeding performance

Eighty-five prepuberal, crossbred gilts received, ad libitum, a diet containing 0 or 10 ppm purified zearalenone for 30 d beginning at 145 to 193 d of age. At the end of this period all gilts were placed on the control diet and exposed daily to a mature boar for 60 d. Within 3 to 5 d of zearalenone ingestion, gilts showed marked vulval swelling and reddening, which continued for the 30-d feeding period. Thereafter symptoms slowly subsided. Zearalenone treated gilts showed first estrus significantly later than controls (P < 0.05), but the proportion of gilts showing estrus within 60 d of boar exposure was similar (P > 0.05). The length of the first estrous cycle was not affected by the ingestion of zearalenone before puberty (P > 0.05). In a second study, 65 multiparous, crossbred sows were full-fed twice daily a ration containing 0 or 10 ppm of purified zearalenone beginning 14 d before weaning. Postweaning, all sows were fed the control diet, were checked for estrus daily, and inseminated at the first postweaning estrus. Neither sows nor gilts from their litters exhibited signs of hyperestrogenism during treatment. Weaning to estrus interval was significantly extended in zearalenone treated sows (P < 0.05), but all other variables of fertility assessed were similar. These data suggest that zearalenone ingestion before puberty delays the stimulation of puberty associated with boar exposure, but does not affect subsequent cyclicity if zearalenone is removed from the ration. Similarly, zearalenone ingestion during lactation delays the return to estrus after weaning, but does not affect subsequent fertility when removed from the ration at weaning.     

Steroidome and metabolome analysis in gilt saliva to identify potential biomarkers of boar effect receptivity

Optimal management of gilt reproduction requires oestrus synchronization. Hormonal treatments are used for this purpose, but there is a growing demand for non-hormonal alternatives, especially in organic farms. The boar effect is an important alternative opportunity to induce and synchronize oestrus without hormones. Before puberty, gilts exhibit a ‘waiting period’ during which boar exposure could induce and synchronize the first ovulation. We searched for salivary biomarkers of this period of boar effect receptivity to improve detection of the gilts to stimulate with the perspective of enhancing the efficacy of the boar effect. Saliva samples were collected from 30 Large-White × Landrace crossbred gilts between 140 and 175 days of age. Gilts were exposed twice a day to a boar and subjected to oestrus detection from 150 to 175 days of age. Among the 30 gilts, 10 were detected in oestrus 4 to 7 days after the first introduction of the boar and were considered receptive to the boar effect, 14 were detected in oestrus more than 8 days after first boar contact, and six did not show oestrus and were considered non-receptive. Saliva samples from six receptive and six non-receptive gilts were analyzed for steroidome and for metabolome using gas chromatography coupled to tandem mass spectrometry and ¹H nuclear magnetic resonance spectroscopy, respectively. Four saliva samples per gilt were analyzed: 25 days and 11 days before boar introduction, the day of boar introduction, 3 days later for receptive gilts or 7 days later for non-receptive gilts. Twenty-nine steroids and 31 metabolites were detected in gilt saliva. Salivary concentrations of six steroids and three metabolites were significantly different between receptive and non-receptive gilts: progesterone and glycolate 25 days before boar introduction, 3α5β20α- and 3β5α20β-hexahydroprogesterone, dehydroepiandrosterone, androstenediol, succinate, and butyrate 11 days before boar introduction, and 3β5α-tetrahydroprogesterone on the day of boar introduction. Thus, nine potential salivary biomarkers of boar effect receptivity were identified in our experimental conditions. Further studies with higher numbers of gilts and salivary sampling points are necessary to ascertain their reliability.     

The effect of early contact with mature boars on reproductive efficiency in the gilt

The effect of first contact of gilts with a mature boar at 23 or 28 weeks of age on their subsequent reproductive efficiency was studied over a 12-month period at a large intensive piggery in southern Australia. Following this contact, the gilts entered the mating shed at 29 weeks of age and were checked daily for oestrus, as assessed by the back-pressure test in the presence of the boar. Gilts that showed moderate or high responses were taken to a boar for mating. Sexual receptivity was then assessed by the time taken to “stand” after the first mount by the boar. Gilts that remained unmated at 35 weeks of age were culled, and their ovaries were examined.Of the 2660 gilts in the study, 2349 were mated and they had a farrowing rate of 88.2% with a mean litter size of 9.5 piglets, of which 0.7 piglets (7.4%) were born dead. The reproductive efficiency of the gilts following earlier contact with the boar was consistently higher than that of gilts exposed later. The mating rate of the week 23 gilts was greater than that of the week 28 gilts (70.1 vs 66.0%, P < 0.01), more appeared to show a high level of sexual receptivity (97.0 and 94.6%, N.S.) and fewer failed to mate when put to a boar (6.1 vs 9.5%, P < 0.01). The percentage of prepubertal gilts at 35 weeks of age was also lower (1.46 vs 3.03%, P < 0.01). The improved reproductive performance was estimated to be equivalent to 0.24 extra piglets born per gilt.     

The effect of the MC4R gene on boar taint compounds,sexual maturity and behaviour in growing-finishing boars and gilts

Societal pressure to ban surgical castration of male piglets is rising due to animal welfare concerns, thus other methods to prevent boar taint need to be explored. Genetic selection against boar taint appears to be a long-term sustainable alternative. However, as boar taint is linked to reproductive hormones, it is important to consider possible negative side effects such as delayed sexual maturity or changes in behaviour. We reported earlier that the melanocortin-4 receptor (MC4R) marker can be used to reduce boar taint levels in fat of boars. The objective of this study was to evaluate whether MC4R marker-assisted selection for lower boar taint prevalence affects plasma levels of boar taint compounds and testosterone; sexual maturity; behaviour; skin lesions; and lameness in boars and gilts. Using an intervention study with a 2×2 design, 264 boars and gilts differing on position 893 of the MC4R gene (AA v. GG) were compared. The MC4R polymorphism did not affect the plasma concentration of either androstenone or testosterone at different time points, whereas the concentration of skatole was significantly lower (P=0.003) and the concentration of indole tended to be lower (P=0.074) in GG compared with AA boars. A higher percentage of gilts of the GG genotype were in puberty at slaughter age compared with AA gilts (P<0.001). The age of the boars at sexual maturity (as indicated by the first positive preputial smear test) did not differ between AA and GG boars. In contrast, weight of GG boars at sexual maturity tended to be lower (P=0.065). During the period from 6 weeks of age to slaughter, boars and gilts of the GG genotype showed more playing behaviour (P=0.015) and less passive and feeding behaviour (P=0.003). They showed more skin lesions on their back and caudal area (P=0.022), and tended to show more skin lesions on their head and anterior area (P=0.093) compared with AA animals. In conclusion, the polymorphism in the MC4R gene can be used as a marker without negative effects on reproduction characteristics in boars and gilts. Genetic selection towards a lower prevalence of boar taint will lead to more active pigs with more skin lesions. Management strategies may therefore be necessary to reduce skin lesions in the selected animals.     

The effects of PG600 and boar exposure on oestrus detection and potential litter size following mating at either the induced (pubertal) or second oestrus

Within gilt pools, incidences of delayed puberty attainment, failure to exhibit regular oestrous cycles and low first litter size are often high. Boar exposure is an effective method of accelerating puberty; however, the timing of gilt response can vary greatly. Although, PG600 (400 IU of PMSG and 200 IU of hCG; Intervet) can induce a rapid and synchronous ovulatory response, thus providing an alternative to boar contact, the quality of the response is often variable. This study compared the effect of PG600, either alone (NBC) or in conjunction with boar exposure (BC), on puberty attainment and maintenance of oestrous cyclicity. The effects of first mating these gilts at the hormonally induced (pubertal) or second oestrus on ovulation rate and early embryo survival were also studied. Eighty Large White cross terminal (Duroc) line gilts were used in this study. The study was conducted in two blocks, with 10 gilts allocated to each of the four treatments in each block. Gilts were artificially inseminated at the allocated oestrus, with the reproductive tracts collected at 26.5+/-0.29 days after first mating (mean+/-S.E.M.), and the number of corpora lutea and viable embryos recorded. Mean days-to-puberty was significantly reduced (P<0.05) when gilts received both PG600 and boar exposure as opposed to PG600 alone (5.7+/-0.15 versus 6.9+/-0.37 days; P<0.01). The proportion of gilts exhibiting an ovulatory response to PG600 was similar for the BC and NBC treatment groups (0.88 and 0.84); however, the proportion of gilts exhibiting visible signs of oestrus in response to PG600 was significantly higher for the BC compared to the NBC treatment groups (0.81 versus 0.49; P<0.05). Boar contact resulted in a numerical, but not significant, increase in the proportion of gilts exhibited a second oestrus (1.00 versus 0.76). There was no significant effect of boar contact on ovulation rate, embryo number or survival. Although ovulation rate was unaffected by oestrus at mating, embryo number was significantly increased (P<0.05) following mating at the second compared to the first oestrus (11.2+/-0.96 versus 7.8+/-1.17). In conclusion, the current data indicate that the timing of puberty attainment and oestrus detection are significantly improved when PG600 treated gilts receive full boar contact. Further, it is evident that mating gilts at their second as opposed to the hormonally induced oestrus significantly increases embryo number at day 26 post-mating.     

Endocrine pattern and external oestrous symptoms at second and fourth oestrus in gilts

The peripheral blood plasma levels of LH, oestradiol-17β and progesterone were recorded during the second and fourth pro-oestrous—oestrous periods in six crossbred (Swedish Landrace X Swedish Yorkshire) gilts. The relationships between hormonal levels, external heat signs and ovarian function were studied.Blood samples were taken every third hour during the pro-oestrous—oestrous periods and during this time the heat detection was performed when blood was collected, otherwise twice daily. The ovaries were inspected by laparoscopy after the first, second and fourth oestrus. The gilts were slaughtered after the fifth oestrus and the genital organs examined.In the five gilts showing five successive regular heats the duration of the second pro-oestrus (reddening and swelling of the vulva) was significantly longer (56.4 ± 5.3 h) than that of the fourth (23.4 ± 6.3 h). The oestrus (standing reflex) duration did not differ, being 51.6 ± 5.4 h for the second and 52.2 ± 9.3 h for the fourth oestrus. The mean oestradiol-17β level was significantly increased during the fourth pro-oestrous—oestrous period (43.9 ± 0.75 pmol) as compared to the second (37.8 ± 0.73 pmol). The LH level was also significantly higher during the fourth (1.61 ± 0.08 μg/l) than during the second pro-oestrous—oestrous period (1.25 ± 0.08 μg/l). There was, however, no difference in the duration of elevated oestradiol levels (> 30 pmol/l). In spite of the higher oestradiol-17β levels, the duration of the external heat signs was reduced during the fourth pro-oestrus when compared to the second. This phenomenon might be explained by a change in susceptibility of vulvar hormonal receptor mechanisms.The sixth gilt displayed three normal heats, but failed to show standing reflex and to ovulate thereafter. The hormonal patterns were normal during the second pro-oestrous—oestrous period. At the expected fourth heat there was a rise of oestradiol but no preovulatory LH peak occurred.     

Failure of the orally active progestin, Regu-mate, to overcome confinement-induced delayed puberty in gilts

Thirty-three crossbred gilts that were raised in total confinement were randomly allotted to two adjacent pens in a finishing unit at 144.7 +/- .5 days of age and 58.0 +/- 1.7 kg body weight. At approximately 253 days of age, 16 gilts were group fed a daily dose of 20 mg of Regu-mate per gilt for 18 days and 17 control gilts were group fed the same diet without Regu-mate for 18 days. Ovarian morphology was examined on 11 or 12 days after the last feeding of Regu-mate. Based on estrous behavior and ovarian morphology only one Regu-mate gilt displayed an estrus but did not ovulate and only three of the control gilts displayed estrus and ovulated at least once before the start of treatment. Three of the 16 Regu-mate gilts displayed estrus and ovulated 7.3 +/- .3 days after the last feeding and within the same time period the 3 control gilts, which previously displayed estrus, continued to have estrous cycles. One additional control gilt displayed estrus and ovulated 5 days after the last feeding of the control diet. Therefore, the proportion of gilts that displayed estrus and ovulated by the end of the experimental period were similar for the treated (25.0%) and control (23.5%) groups. Based on these results we conclude that treatment of gilts in a state of confinement-induced delayed puberty with 20 mg Regu-mate daily for 18 days failed to result in a synchronized onset of puberty in a significant proportion of gilts.     

Effects of composition and density of the group on the performance,behaviour and age at puberty in swine

Two hundred and eighteen cross-bred pigs (Duroc × Hampshire × Landrace × Yorkshire) were assigned to a 3 × 2 factorial experiment; the factors being composition of the group and density. The composition of the group factor consisted of pigs not reaggregated (NR), re-aggregated below the median body weight (RBMW), and re-aggregated above the median body weight (RAMW) at the time of transfer to the finishing pens. The density factor consisted of groups of 6 or 12 pigs/pen. Two trials with 2 replications of each trial were conducted. Twenty-six gilts from Trial I were used to determine their age and ovulation rate at the pubertal oestrus. During the nursery phase, composition of the group had no effect (P>0.05) on average daily feed intake (ADFI) or feed efficiency (F/G). Pigs in the NR and RAMW groups had a similar (P>0.05) average daily gain (ADG), whereas, those pigs in the RBMW group gained (P<0.05) at a slower rate. Pigs housed in groups of 6 had a higher (P<0.05) ADFI, had similar (P>0.05) ADG and poorer (P<0.05) F/G than those housed in groups of 12. During the finishing phase, composition of the group had no effect (P>0.05) on ADFI, ADG or F/G. Pigs housed in groups of 6 had a greater (P<0.05) ADFI and ADG, but similar (P<0.05) F/G compared to those housed in groups of 12. Correlation coefficients between the various behaviours and the performance variables suggested that the more active pens of pigs gained less per day and were less efficient. Gilts housed in the NR groups of 6 were younger (P<0.05) at puberty than gilts in the other groups of 6 or 12. Also, gilts housed in the RBMW groups of 6 were younger (P<0.05) at puberty than those housed in the RAMW groups of 6, whereas those housed in the RBMW groups of 12 were older (P<0.05) at puberty than those housed in the RAMW groups of 12. Ovulation rate was not affected (P>0.05) by composition of the group, density or their interaction. In summary, composition and density of the group affected the performance of pigs and was correlated to some of the behavioural measurements. The most noticeable effect was that these same factors caused a delay in the onset of puberty in gilts.     

The effects of two oestrus detection procedures and intense boar stimulation near the time of oestrus on mating efficiency of the female pig

In the first experiment, a higher oestrus detection rate (percentage of cycling gilts that were detected in oestrus) and a higher mating rate (percentage of cycling gilts that were mated) were achieved when cycling gilts were checked for oestrus in the corridor adjacent to the boar pens than when they were checked in their own pens, which were separated from the boar pens by a 1.0 m-wide corridor (90 v. 52% and 87 v. 52%, respectively). In the second experiment, several housing treatments were imposed over a 21-day period. A lower proportion of gilts were detected in the I stage of oestrus (positive response to the back-pressure test both in the presence and absence of a boar) and a lower mating rate was achieved when cycling gilts were separated from the boar by a wire-mesh pen division than when separated by a 1.0 m corridor (48 v. 81% and 47 v. 81%, respectively). It was concluded that cycling females should be housed near, but not adjacent to, boars and that at the time of oestrus detection using the back-pressure test, females should be very close to boars.     

Effects of oestrous synchronization with altrenogest in gilts on endometrial and embryonic characteristics

The use of altrenogest (ALT) supplementation for oestrous synchronization improves subsequent reproductive performance of gilts and sows. However, the causes of this improvement in reproductive performance after ALT treatment are not fully/clearly understood. The objective of this study was to evaluate the effects of ALT supplementation for oestrous synchronization in gilts on the endometrial glands and embryonic development characteristics at 28 days of pregnancy. Pregnant gilts were divided into two experimental treatments: Control (did not receive ALT; n = 9 gilts) and ALT (ALT feeding at 20 mg/day for 18 days; n = 9 gilts). At 28 days of pregnancy, six gilts from each treatment were slaughtered, and reproductive tracts were immediately evaluated. There was no statistical difference (P > 0.05) between treatments regarding ovulation rate, number of embryos, number of vital embryos and number of non-vital embryos. Embryo weight, length and embryonic vesicle weight were lower in ALT treatment compared with Control (P < 0.01), and it was lower in the cervical uterine region compared with apex uterine region, respectively (P < 0.05). Higher values of gland duct area, gland duct perimeter, percentage of the glandular area and total endometrial area were observed in ALT treatment compared with Control (P < 0.05). The use of ALT during 18 days for oestrous synchronization in gilts increased the gland duct area, perimeter and total endometrial area but did not increase the embryo number and embryo size at day 28 of pregnancy.