Changes in the electric resistance of the vaginal mucus in oestrous sows

Changes in the electric resistance of the vaginal mucus were monitored in a large pig herd at 4-h intervals with a heat detector (Hauptner, Federal Republic of Germany) in multiparous sows (n = 16; litter size = 11.4 +/- 2.9) that showed a positive standing test and conceived. The initial value of resistance was 74.4 +/- 7.4 ohms. In 36 h this value gradually increased to 93.6 +/- 7.6 ohms. One to 2 h after the artificial inseminations (AI) lower resistance values were obtained, though the difference was not statistically significant. In the second part of the experiment 73.9% and 82.7% of the gilts (n = 92) and multiparous sows (n = 98) conceived, respectively, with an average litter size of 9.6 +/- 2.2 and 11.0 +/- 2.7, respectively. The conception rate of animals that immediately before AI had vaginal mucus resistance values between 75 and 90 ohms was about 20% higher. The only exception were 8 multiparous sows which had an average vaginal mucus resistance of 70 +/- 4.6 ohms after the first insemination. Litter size was also the biggest in sows with vaginal mucus resistance between 75 and 90 ohms. This difference was statistically significant for the multiparous sows. The heat detector is considered to be a useful complement to conventional methods of oestrus detection.     

Factors influencing estrus and ovulation in weaned sows as determined by transrectal ultrasound.

Characterization of factors influencing estrus and ovulation in sows may facilitate development of procedures for improving reproductive performance. The experiment was conducted in confinement during 1997 to 1999 using 174 Large White x Landrace sows. After weaning, sows were checked for estrus twice daily. In the 1st yr, transrectal ultrasound was performed once daily and in the 2nd yr twice daily at estrus and on every day until ovulation. The effects of lactation length (< or = 16 d, 17 to 24 d, 25 to 31 d or > or = 32 d), parity (1, 2, or > or = 3), season (winter, spring, summer, or fall) and weaning-to-estrus interval (3, 4, 5, or 6 to 8 d) and their interactions on estrual and ovulatory responses were studied. There was no effect of frequency of ultrasound on any response variable, so data across years were pooled. Percentage of sows expressing estrus within 8 d of weaning was influenced by lactation length (P < 0.001), with sows lactating < or = 16 d (35.2%) less likely to express estrus than sows lactating > or = 17 d (94%). A parity x season interaction was observed (P < 0.001) for estrus, with the lowest expression in parity 1 (73.0%) and parity 2 sows in fall (67.2%), compared with > or = parity 3 sows (98.1%). No explanatory variable had a significant effect on weaning-to-estrus interval (4.4 d) or on follicle size at estrus (8.1 mm). Ovulation hour after onset of estrus was affected by weaning-to-estrus interval (P < 0.01), with sows returning in 3 d ovulating at 46.2 h and between 6 and 8 d at 30.2 h. For sows that expressed estrus within 8 d of weaning, the percentage of sows ovulating was influenced by lactation length (P < 0.001) and weaning-to-estrus interval (P < 0.001). Sows that lactated < or = 16 d were less likely to ovulate (78.0%) than those lactating > or = 17 d (> 92%). Sows that returned to estrus in 3 d were also less likely to ovulate (79.5%) than sows returning > or = 4 d after weaning (> 92%). A parity x season interaction was also observed on ovulation (P < 0.001), with parity 1 and 2 sows less likely to ovulate after expressing estrus in fall and spring compared with parity 3 and greater sows. The data suggest lactation length, early return to estrus, and parity by season effects are associated with risk of failure to express estrus and ovulate.     

Responsiveness to boar stimuli and change in vulvar reddening in relation to ovulation in weaned sows

In 117 weaned sows, changes in estrous behavior and vulvar reddening were related to timing of ovulation. Detection of estrus was performed every 8 h with four levels of boar stimuli to record the change in responsiveness to these stimuli. This resulted in four overlapping phases of estrus, during which a standing response could be evoked: 1) man estrus (standing response to a back pressure test, in the absence of a boar), 2) spontaneous estrus (standing response in the presence of a boar, no back pressure test), 3) boar estrus (standing response to boar + back pressure test), and 4) detection-mating-area estrus (back pressure test in the presence of four boars). In addition to the detection of estrus, the change in reddening of the inner vulvar mucosa was recorded. Manifestation of estrus in response to the four stimuli occurred in 46, 56, 90, and 97% of the sows, respectively. Onset of the four phases occurred 24 h (SD 13 h), 23 h (SD 15 h), 34 h (SD 13 h), and 41 h (SD 12 h) before ovulation. The duration of the intervals between the various phases of estrus explained 10 to 50% of the variation in the timing of ovulation relative to the onset of the phases. However, these intervals could not be calculated for all sows because estrus was not expressed at every stimulus level by each sow. The end of vulvar reddening occurred, on average, 21 h (SD 14 h) before ovulation. Except for five sows that ceased to show vulvar reddening within 5 h after ovulation, the end of vulvar reddening occurred before ovulation, within a 70-h range. Of the sows showing boar estrus, 90% also showed vulvar reddening. For sows that showed vulvar reddening until after the onset of boar estrus (two-thirds of the sows), the end of reddening occurred within a much smaller range: from 36 h before, until 2 h after, ovulation. Onset of estrus, regardless at which stimulus level it is detected, appears too variable relative to timing of ovulation to be used as a predictor for ovulation. Duration of the different stages of responsiveness explains only some of this variation and cannot be obtained on all sows. Combining information on vulvar reddening and boar estrus can predict ovulation within a reasonable range for two-thirds of the sows.     

定时输精对母猪繁殖性能的影响

为了研究同期发情+定时输精对母猪发情率、妊娠率及产仔数的影响。试验1:将200头后备母猪随机分成两组,每组100头。所有后备母猪连续饲喂四烯雌酮(ATL)(15 mg/d)14 d,第15 d开始查情。试验组后备母猪停止饲喂ATL 24 h后肌注促性素(PMSG)、再过72 h肌注生源(Gn RH),肌注Gn RH 24 h后开始输精1次,过24 h再输精1次;对照组后备母猪停止饲喂四烯雌酮后有发情就开始输精,过24 h再输精1次(如还发情,第2次输精过24 h后再输精1次);试验2:将200头断奶母猪随机分成两组,每组100头,断奶第2 d开始查情。试验组断奶母猪断奶24 h后肌注促性素(PMSG),再过72 h肌注生源(Gn RH),肌注Gn RH 24 h进行输精1次,过24 h再输精1次;对照组断奶母猪发情就开始输精,过24 h再输精1次(如还发情,第2次输精过24 h后再输精1次);精液剂量为80 ml(2×109个精子细胞)。试验1结果显示,试验组的后备母猪的静立率(P>0.05)、妊娠率(P<0.05)、分娩率(P<0.05)、窝产仔数(P>0.05)均高于对照组。试验2结果显示,试验组的断奶母猪的发情率、妊娠率、分娩率均高于对照组(P>0.05),窝产仔数也高于对照组。试验结果表明,母猪肌注PMSG和Gn RH,可改善母猪的发情率、分娩率、窝产仔数,减少隐性发情母猪的漏配率。     

The correlation between the cytology of the vaginal smear and the time of ovulation in the bitch

The correlation between the vaginal smear and the calculated time of ovulation was studied in 22 bitches, during a total of 24 heat periods. Blood plasma was analysed for levels of oestradiol and progesterone from 6 days before to 6 days after the day of maximum keratinization of the vaginal smear. In all 24 heat periods (100 per cent) maximum keratinization of the vaginal epithelial cells was observed at least 3 days after peak oestradiol levels and in 17 of the heat periods (70.8 per cent) maximum keratinization was seen when the peripheral plasma level of progesterone had increased to >5.44 ± 0.93 ng/ml, which has been calculated as the ovulatory level.     

Association between physical properties of cervical mucus and ovulation rate in superovulated cows

Possible associations between certain physical properties of cervical mucus (CM) and ovulation rate were studied in 21 superovulated Holstein cows. In CM samples collected at the beginning of estrus (0 h) and in 4 h intervals for the following 24 h, the pH, the spinnbarkeit (spinability), and the crystallization value were measured. Blood samples, collected at the same time points with CM samples, were assessed for progesterone and estradiol concentrations. At 48 h the number of ovulated follicles was counted by transrectal ultrasonography and the animals were allotted into 2 groups according to the occurrence of at least one (group A, n = 16) or no (group B, n = 5) ovulations. The pH was lower (P < 0.05) at 8 h (7.00 + 0.24) in group A compared with group B (7.55 + 0.12). In group A, spinnbarkeit was significantly lower at 0 h and 20 h, and higher at 8 h and 16 h compared with group B (0 h: 2.50 + 0.82 versus 6.95 + 0.41; 20 h: 3.00 + 1.89 versus 5.38 + 0.94; 8 h: 7.00 + 0.87 versus 2.75 + 0.43; 16 h: 7.00 + 1.41 versus 4.30 + 0.71, for groups A versus B, respectively). Crystallization was significantly lower at 4 h (2.00 + 0.63) and 20 h (1.50 + 0.82) in group A compared with group B (3.13 + 0.32 at 4 h and 3.00 + 0.41 at 20 h). Progesterone at all time points, and estradiol at 16 h, 20 h, and 24 h were lower (P < 0.05) in group A than in group B. The pH, crystallization, estradiol, and progesterone differed (P < 0.05) within one group, while sbk differed within both groups.Our results imply that during the periovulatory period, steadily low progesterone concentrations trigger alterations of certain CM characteristics, while extremely high estradiol concentration could prevent the occurrence of these alterations.     

Hormonal therapy for sows weaned during fall and winter

Sows from five commercial herds were weaned in the fall and winter and used to ascertain the potential application of hormonal therapy to stimulate subsequent litter size born. At weaning sows within parity (1, 2, and 3 through 6) and lactation length classification (early weaned, < or = 14 d; conventionally weaned, > 14 d) were randomly assigned to treatment. Treatments were injection with P.G. 600 (400 IU PMSG with 200 IU hCG) at weaning or no treatment. Sows were individually observed for estrus and mated following protocol for each herd. Breeding, culling, and farrowing data were collected. Treatment with P.G. 600 did not change subsequent rebreeding performance for sows at parity 1 or parities 3 through 6. However, conventionally weaned parity-2 sows treated with P.G. 600 were more likely (P < .05) to return to estrus than conventionally weaned controls (99.0 vs 93.6%, respectively). For parity-1 and parity-2 sows, treatment did not significantly change the likelihood for farrow percentage. However, the likelihood to farrow a litter was greater (P < .05) among P.G. 600-treated sows at parities 3 to 6 that were conventionally weaned (84.4 vs 71.3%, respectively). Subsequent litter birth weight for parity-1 sows treated with P.G. 600 was lower (P < .02) than for controls (15.6 vs 16.6 kg, respectively). Subsequent litter size at birth was not affected by treatment for parity-1 or parity-2 sows compared with controls. However, early-weaned sows at parities 3 through 6 treated with P.G. 600 had more (P < .06) total number born than controls (12.4 vs 10.6, respectively). Treatment with P.G. 600 improved reproductive function within specific parity and lactation length classification for sows weaned in the fall and winter.     

提高夏季断奶母猪发情率的几点措施

<正>广东省地处热带和亚热带季风气候区,每年夏季,平均气温为28～29℃,6～8月份最高气温达到36～38℃,且持续较久,给养猪生产带来极为不利的影响,表现为母猪发情率等生产指标明显下降。断奶母猪发情率,与其他月份相比往往下降20%～40%,甚至出现暗发情或发情状态很不稳定,造成配种后返情率很高,一定程度上困扰养猪生产。这可以从我场2008年全年一个单元内断奶母猪的发情率进行比较(见表1)。鉴于此,笔者从防暑降温工作落实、改善母猪膘情、改变查情时间等方面谈谈提高断奶母猪发情率的一些看法。     

丹系母猪断奶后发情和排卵规律的研究

母猪适时配种是提高受胎率的关键措施之一,而决定配种时间的主要依据是母猪排卵时间。本研究采用B超探测技术对56头不同胎龄的丹系高产母猪发情后的排卵规律进行观测研究。结果发现,母猪断奶后发情至排卵间隔平均为(29.28±8.14)h,排卵持续时间平均是(14.64±4.07)h;母猪断奶至发情间隔为4 d时,母猪发情至排卵间隔和排卵持续时间与其他组差异均显著(P0.05);当断奶至发情天数从2 d增加到5 d,发情至排卵间隔平均减少4.78 h,排卵持续时间平均减少2.39 h;哺乳期小于25 d的母猪断奶到发情间隔及排卵间隔与其他两组母猪均差异显著(P0.05);不同哺乳期的母猪排卵持续时间差异不显著(P0.05);胎次对母猪发情排卵时间存在一定的影响,高胎次母猪比低胎次母猪断奶后发情较迟,排卵持续时间也较长。     

母猪配种前后气候因子与窝产仔数的关系

本文分析了某猪场１９９３年３月至１９９４年３月之间１７２２胎窝产仔数，夏季（１９９３年６月至９月份）配种所产仔猪数显著低于其它月份（Ｐ〈０．０５）。母猪配种时期气候因素如平均日照，温度，相对湿度和风速与窝产仔猪数的相关系分别为－０．５１６，－０．７７５，－０．２８１，－０．７５１，用通径分析法对以上相关系及各气候因子间的相关系进行部分，求出以上各气候因子以窝产仔猪数的通径系数分别为０．５０７，－０     

Effect of housing system and boar exposure on estrus expression in weaned sows

Reproductive efficiency depends on detection of estrus, which may be influenced by housing and boar exposure. This experiment investigated the effects of housing system and boar contact on measures of estrus in weaned sows. Mixed-parity sows were randomly assigned to be weaned into gestation crates away from boars (AWC, n = 45), into pens away from boars (AWP, n = 42), or into pens adjacent to a mature boar (ADJ, n = 46). Estrus detection was initiated at approximately 0700 (0 h) and again at 0.25-, 0.5-, 1-, 2-, 4-, and 8-h intervals beginning on d 4 and continuing through d 7 following weaning. Estrus detection involved observation of the standing response after application of nose-to-nose boar exposure, backpressure, and side rubbing. For the AWC sows, a mature boar was moved to the front of the crates for a 10-min period and then removed. Sows housed in AWP were moved approximately 15 m to an empty pen adjacent to a mature boar for a 10-min period, and then returned to their pen. Sows housed ADJ were not moved and estrus detection was performed in their home pen for a 10-min period. The proportion of sows expressing estrus within 7 d from weaning was lowest for ADJ (80%, 37/46) compared with AWP (98%, 41/42) and AWC (96%, 43/45; P < 0.05). There was an effect of interval from weaning to estrus on the percentage of sows expressing estrus, but there was no interaction with treatment. Sows in AWC and AWP (4.7 d) had decreased (P = 0.01) intervals from weaning to estrus compared with ADJ (5.2 d). The duration of estrus was also shorter (P < 0.001) for ADJ (45 h) compared with AWC (58 h) or AWP (62 h). There was a treatment x interval x day of estrus effect for the percentage of sows expressing estrus. After detection of the first standing response on the first day of estrus, only 62 to 82% of sows were detected standing over the next 2 h for all treatments. However, at 4 to 8 h, this increased to 85 to 98% for the AWC and AWP sows, but <73% of the ADJ sows were detected during this period. On the second day of estrus, estrus expression was not influenced by interval for the AWC and AWP sows and was between 90 to 100% during the 8-h period, whereas ADJ sow detection rates were between 68 to 88%. These data suggest that housing sows adjacent to boars negatively affects estrus expression and detection. In addition, refractory behavior occurs in approximately 30 to 40% of sows and is influenced by housing relative to the boar, day of estrus, and interval from last boar exposure.     

Early embryo survival and development in sows with lactational ovulation.

During lactation, daily separation of sow and piglets, intermittent suckling (IS), can induce lactational oestrus and ovulation. This study examined effects of IS on subsequent early embryo survival and development. Multiparous Topigs40 sows were separated from their piglets for either 12 consecutive hours per day (IS12, n = 13) or two times for 6 h per day (IS6, n = 10) from day 14 of lactation onwards until 23 days after ovulation. Control sows (C, n = 17) were weaned at day 21 of lactation. Oestrus was shown in all treatments within 5 days after the start of treatment. Sows were inseminated each day of oestrus and slaughtered at D23 after ovulation. Intermittent suckling did not significantly affect pregnancy rates of sows (75% IS12 vs 78% IS6 vs 94% C; p > 0.10). Embryo survival was not significantly affected by IS (IS12: 57%; IS6: 51%; p > 0.10) although it seemed to be lower than in C sows (70%). Some parameters of embryo, placental and uterine development were affected by IS, especially in the IS6 group. IS6 embryos had shorter placentas (17.5 +/- 1.2 cm; p < 0.05) than C (20.3 +/- 1.4 cm) and IS12 sows (20.9 +/- 0.7 cm) were smaller and less developed than C sows (p < 0.05). In conclusion, embryo survival does not seem significantly affected by IS, although numerical differences were great. Embryo development, however, was negatively affected in IS6 sows possibly due to a combination of high milk production, stress and lactational effects on uterine development.     

Effects of boar contact and housing conditions on estrus expression in weaned sows

Our objective was to study the effects of housing conditions and the amount of boar contact in a protocol for estrus detection on estrus detection rate, timing of onset of estrus, duration of estrus, and timing of ovulation. After weaning, 130 multiparous sows were assigned to three treatments: HI, in which 52 sows were housed individually in crates and received a high amount of boar contact during estrus detection; HG, in which 52 sows were housed in groups and received a high amount of boar contact; and NI, in which 26 sows were housed individually in crates and received a normal amount of boar contact. Estrus detection was performed every 8 h. For each treatment, the standing response to three levels of stimuli was recorded: a back pressure test (BPT) by a man (man-estrus), presence of a teaser boar (spontaneous-estrus), and BPT in the presence of a teaser boar (boar-estrus). In addition, for HI and HG, the standing response to a fourth level of stimuli was recorded: BPT in a detection-mating area, surrounded by four boar pens (DMA-estrus). To detect ovulation, ultrasonography was performed every 4 h during estrus. Of 117 sows that ovulated, 46% showed man-estrus, 56% spontaneous-estrus, 90% boar-estrus, and 97% DMA-estrus. Mean onset of man-estrus was 107 h (SD 26) after weaning, of spontaneous-estrus was 106 h (SD 22) after weaning, of boar-estrus was 99 h (SD 21) after weaning, and of DMA-estrus was 93 h (SD 22) after weaning. Duration of man-estrus was 22 h (SD 14), of spontaneous-estrus was 29 h (SD 16), of boar-estrus was 42 h (SD 20), and of DMA-estrus was 55 h (SD 18). The high amount of boar contact reduced the number of sows showing man-estrus (P < .05; 41% for HG and HI vs 68% for NI) and reduced duration of boar-estrus (P < .05; 43 h for HG and HI vs 52 h for NI). Duration of DMA-estrus for HG and HI was similar to duration of boar-estrus for NI. Onset of estrus and timing of ovulation were not affected by amount of boar contact. Group housing did not affect detection rate and duration of estrus, but it did postpone average onset of estrus by 10 h, paralleled by a postponement of ovulation. In conclusion, estrus expression is similar at the highest level of stimuli in different protocols for estrus detection. Including higher levels of stimuli in a protocol reduces estrus expression at lower levels of stimuli. This reduction indicates adaptation of sows to a given protocol for estrus detection. Group housing can delay ovulation and related behavioral estrus.     

Relationship between body fat and postweaning interval to estrus in primiparous sows

Twenty-two primiparous Yorkshire sows were used to determine whether a minimal threshold of body fat exists below which the return to estrus is delayed. A second objective was to examine the relationship between body fat and interval from weaning to estrus in restricted-fed sows. During lactation (28 d), sows received 7, 9, 11 or 13 Mcal of ME daily to produce a range of sow body fatness at weaning. Intake of all dietary essentials except ME was similar for all sows. Litter size was adjusted to 10 pigs for all sows by d 3 postpartum. Each day from weaning to estrus, sows received 110 kcal ME per kg metabolic body weight plus 1,359 kcal ME per sow. Body fat was estimated at weaning and at first postweaning estrus by deuterium oxide dilution. Last rib backfat depth was determined ultrasonically 24 h postpartum and at weaning. Irrespective of dietary ME intake, percentage body fat at weaning (R2 = .24; P less than .05) and first postweaning estrus (R2 = .03; P greater than .50) accounted for only a small portion of variation in interval from weaning to estrus. Likewise, loss of backfat depth during lactation was not an accurate predictor of interval from weaning to estrus (R2 = .24; P less than .05). The low coefficients of determination (less than .25) suggest that body fat is a minor controller of postweaning interval to estrus. In contrast, dietary ME intake during lactation accounted for the largest portion of the variation (R2; = .48; P less than .01) in postweaning interval to estrus. We conclude that timing of postweaning estrus in primiparous sows is not dependent on a minimal threshold of body fat. Furthermore, effects of lactational ME intake on the postweaning interval to estrus are more pronounced than the effects of body fat.     

Relationship between certain physical properties of cervical mucus and fertility in cows

The object of the present investigation was to determine several physical properties of cervical mucus in spontaneous oestrus cows in relation to fertility. Because, it is very difficult to determine the exact time of the beginning of oestrus in cows, the aim of the present study was to investigate if physical properties of cervical mucus at the time of artificial insemination (AI) are related to conception or not. A total of 93 cows of Friesian breed were used. The animals exhibited spontaneous oestrus, without being submitted to any hormonal treatment. Samples of cervical mucus were collected 5-30 min before AI and pH, viscosity, spinnbarkeit (spinability), crystallization and penetration were measured. Pregnancy diagnosis was performed by rectal palpation 3 months later. The results obtained from cows that conceived (44 animals), compared to those obtained from cows that did not conceive (49 animals), were the following: a) viscosity had been significantly lower (p < 0.05), b) crystallization had been significantly higher (p < 0.05), and c) pH, spinnbarkeit and penetration of spermatozoa into cervical mucus did not differ. In conclusion, the best time for AI is when viscosity is below 20 mm H2O and crystallization is above 3. Viscosity and crystallization could be related to ovulation time, but this needs further investigation.     

乳化均衡油粉在哺乳母猪及断奶仔猪日粮中的应用效果试验

随着养殖业的迅速发展,养殖企业为了不断提高养殖效益和管理水平,以降低成本或增加产值来提高利润空间。据生产实践,养猪业之间的竞争主要集中在猪的增重率和饲料利用率。母猪哺乳期间泌乳量的高低和质量优劣直接关系到哺乳仔猪的增重速度及健康水平,提高哺乳期间哺乳仔猪的增重速度和提高免疫力是整个养猪过程的关键所在。