Relationship between litter birth weight and litter size in six breeds of sheep

Metabolizable energy requirements of the ewe increase during pregnancy due to increases in fetal and maternal metabolism. Fetal metabolism is related to total weight of the fetuses. Fetal number is a primary contributor to fetal weight. Litter birth weight represents the culminated fetal growth of the litter and can be used to estimate the effect of fetal metabolism on energy requirements of the ewe. We hypothesized that litter weight in sheep would increase at a decreasing rate with increasing litter size. Birth weights of lambs born to yearling (11 to 15 mo) and mature ewes (> 34 mo) were collected on litters born to Dorset, Rambouillet, Suffolk, Finnsheep, Romanov, and Composite III ewes mated to produce straightbred lambs. Litter birth weight expressed as a function of litter size increased at a decreasing rate and the quadratic term differed from zero for mature Rambouillet, Suffolk, Finnsheep, Romanov, and Composite III litters (P < 0.042). The quadratic coefficient differed among breeds. In yearlings, litter weight increased at a decreasing rate for Suffolk ewes (P = 0.002). The quadratic term for the relationship between litter weight and litter size did not differ from zero for Finnsheep (P = 0.39) or Romanov litters (P = 0.07). The hypothesis that litter weight increases at a decreasing rate with increased litter size is supported by experimental results.     

饲喂大米草对波尔山羊产羔数、羔羊初生重和体尺指标的影响

文章旨在研究饲喂大米草对纯种波尔山羊的产羔数、羔羊初生重以及羔羊体尺指标的影响。结果表明:饲喂大米草对波尔山羊产羔数、羔羊初生重和羔羊体尺指标等具有一定的影响。其中试验组与对照组双羔的初生重和胸围指标达到差异显著水平(P<0.05)。     

Genetic determination of individual birth weight, litter weight and litter size in Mukota pigs

Genetic parameters for individual birth weight (IBWT), total number of pigs born (NBT), number of pigs born alive (NBA), number of pigs born dead (NBD) and litter weight at birth (LBWT) were estimated using 1961 Mukota pigs kept at the University of Zimbabwe Farm, Harare, Zimbabwe. Variance components were estimated for IBWT based on a direct-maternal genetic effects model. The genetic relationships among NBT, NBA, NBD and LBWT were assessed using a multi-trait direct effects model. For LBWT, the direct, maternal and common environmental litter proportions on the phenotypic variance were 0.090, 0.033 and 0.009, respectively. After adjustment of IBWT for NBA, phenotypic fractions were 0.091, 0.034 and 0.011 for direct, maternal and litter effects. The correlation between the direct and maternal genetic effects of IBWT was − 0.354 and − 0.295, with and without adjustment for NBT. Heritabilities for NBT, NBA, NBD and LBWT were 0.020, 0.030, 0.088 and 0.196, respectively. Differences in the maternal heritability and the heritability for LBWT, a trait of the dam, are different due to accumulation of observations per litter. Maternal genetic effects are, therefore, of less importance than in highly selected European breeds.     

Bayesian analysis of birth weight and litter size in Baluchi sheep using Gibbs sampling

Variance and covariance components for birth weight (BWT), as a lamb trait, and litter size measured on ewes in the first, second, and third parities (LS1 through LS3) were estimated using a Bayesian application of the Gibbs sampler. Data came from Baluchi sheep born between 1966 and 1989 at the Abbasabad sheep breeding station, located northeast of Mashhad, Iran. There were 10,406 records of BWT recorded for all ewe lambs and for ram lambs that later became sires or maternal grandsires. All lambs that later became dams had records of LS1 through LS3. Separate bivariate analyses were done for each combination of BWT and one of the three variables LS1 through LS3. The Gibbs sampler with data augmentation was used to draw samples from the marginal posterior distribution for sire, maternal grandsire, and residual variances and the covariance between the sire and maternal grandsire for BWT, variances for the sire and residual variances for the litter size traits, and the covariances between sire effects for different trait combinations, sire and maternal grandsire effects for different combinations of BWT and LS1 through LS3, and the residual covariations between traits. Although most of the densities of estimates were slightly skewed, they seemed to fit the normal distribution well, because the mean, mode, and median were similar. Direct and maternal heritabilities for BWT were relatively high with marginal posterior modes of .14 and .13, respectively. The average of the three direct-maternal genetic correlation estimates for BWT was low, .10, but had a high standard deviation. Heritability increased from LS1 to LS3 and was relatively high, .29 to .37. Direct genetic correlations between BWT and LS1 and between BWT and LS3 were negative, -.32 and -.43, respectively. Otherwise, the same correlation between BWT and LS2 was positive and low, .06. Genetic correlations between maternal effects for BWT and direct effects for LS1 through LS3 were all highly negative and consistent for all parities, circa -.75. Environmental correlations between BWT and LS1 through LS3 were relatively low and ranged from .18 to .29 and had high standard errors.     

Effects of breed, heterosis, age of dam, litter size, and birth weight on lamb mortality

Sources of individual plus maternal effects on lamb mortality were studied in data collected at the U.S. Meat Animal Research Center from 1980 to 1985 for paternal and maternal breeds lambing yearly and for maternal breeds lambing at 8-mo intervals. Records included 16,881 lambs born. Breeds included were Finnsheep (F), Dorset (D), Rambouillet (R), Suffolk (S), Targhee (T), Composite 1 (C1 = F/2, D/4, R/4), Composite 2 (C2 = F/2, S/4, T/4), and Composite 3 (C3 = Columbia/2, S/4, Hampshire/4), Traits analyzed were perinatal, postnatal, and total mortality to 60 d of age and postnatal respiratory, digestive, starvation, injury, and other or unknown causes of mortality. The least squares analyses included breed, year, sire within breed-year, sex, linear and quadratic season and age of dam covariates (Model 1), plus litter size (Model 2), plus birth weight (Model 3), and significant two-way interactions. Age of dam, litter size, and birth weight all had important, often quadratic, effects that differed among breeds. Models 1, 2, and 3, respectively, reduced variation by 8, 10, and 16% for perinatal, 7, 8, and 12% for postnatal, and 9, 11, and 20% for total mortality. In Model 1, breed means ranged from 3.5 to 16.2% for perinatal, 7.2 to 21.1% for postnatal, and 16.7 to 32.8% for total mortality. Respiratory and starvation problems were major causes of postnatal mortality. Heterosis for lamb survival retained in composites was 9% for C1 and 18% for C2. Mortality was 1 to 5% higher for males than for females.(ABSTRACT TRUNCATED AT 250 WORDS)     

Genetic parameters for individual birth and weaning weight and for litter size of Large White pigs

Data from a French experimental herd recorded between 1990 and 1997 were used to estimate genetic parameters for individual birth and weaning weight, as well as litter size of Large White pigs using restricted maximum likelihood (REML) methodology applied to a multivariate animal model. In addition to fixed effects the model included random common environment of litter, direct and maternal additive genetic effects. The data consisted of 1928 litters including individual weight observations from 18 151 animals for birth weight and from 15 360 animals for weaning weight with 5% of animals transferred to a nurse. Estimates of direct and maternal heritability and proportion of the common environmental variance for birth weight were 0.02, 0.21 and 0.11, respectively. The corresponding values for weaning weight were 0.08, 0.16 and 0.23 and for litter size 0.22, 0.02 and 0.06, respectively. The direct and the maternal genetic correlations between birth and weaning weight were positive (0.59 and 0.76). Weak positive (negative) genetic correlations between direct effects on weight traits and maternal effects on birth weight (weaning weight) were found. Negative correlations were found between direct genetic effect for litter size and maternal genetic effects on all three traits. The negative relationship between litter size and individual weight requires a combined selection for litter size and weight.     

Genetic parameters for individual birth and weaning weight and for litter size of Large White pigs

Data from a French experimental herd recorded between 1990 and 1997 were used to estimate genetic parameters for individual birth and weaning weight, as well as litter size of Large White pigs using restricted maximum likelihood (REML) methodology applied to a multivariate animal model. In addition to fixed effects the model included random common environment of litter, direct and maternal additive genetic effects. The data consisted of 1928 litters including individual weight observations from 18151 animals for birth weight and from 15360 animals for weaning weight with 5% of animals transferred to a nurse. Estimates of direct and maternal heritability and proportion of the common environmental variance for birth weight were 0.02, 0.21 and 0.11, respectively. The corresponding values for weaning weight were 0.08, 0.16 and 0.23 and for litter size 0.22, 0.02 and 0.06, respectively. The direct and the maternal genetic correlations between birth and weaning weight were positive (0.59 and 0.76). Weak positive (negative) genetic correlations between direct effects on weight traits and maternal effects on birth weight (weaning weight) were found. Negative correlations were found between direct genetic effect for litter size and maternal genetic effects on all three traits. The negative relationship between litter size and individual weight requires a combined selection for litter size and weight.     

Effect of litter size and birth weight on growth, carcass and pork quality, and their relationship to postmortem proteolysis

The objective of the study was to test the hypothesis that birth weight (BtW) influences growth, carcass characteristics, meat quality, and postmortem (pm) proteolysis differently when pigs originate from small (S) or large (L) litters. Swiss Large White barrows (60) used in this study originated from 20 litters with either less than 10 (S) or more than 14 (L) piglets born per litter. Within each of the S and L litters, 3 barrows were selected at birth: the lightest (L-BtW), the heaviest (H-BtW), and the one with a BtW nearest to the average BtW of the litter (M-BtW). The BW and total feed intake of the individually penned pigs were determined weekly. At slaughter, carcass characteristics were assessed. Meat quality traits were determined in the LM and dark portion of semitendinosus muscle. Titin, nebulin, desmin, and integrin proteolysis were evaluated by SDS-PAGE and Western blot technique, and mu - and m-calpain activities were monitored using casein zymography. Litter size affected BtW of L-BtW and M-BtW but not of H-BtW barrows (BtW x litter size interaction; P = 0.07). From weaning to slaughter, L-BtW barrows grew slower (P < 0.01), ingested less feed (P < 0.01), and were less efficient (P < 0.01) than H-BtW and M-BtW barrows. The carcass yields were greater (P < 0.01), and livers and kidneys were lighter (P 相似文献   

影响母猪产仔数和仔猪初生重的因素

繁殖率是反映母猪繁殖力和猪场生产管理水平的重要经济参数。通常衡量母猪群生产性能的指标是每头母猪每年提供的断奶仔猪数,主要有两部分组成,即年母猪产仔窝数和母猪每窝的断奶仔猪数。据生产实践,有许多因素影响着母猪的生产性能,包括遗传因素、环境因素、饲养管理因素等。饲养母猪,只有年产仔窝数多,     

Maintenance of body temperature in the neonatal lamb: effects of breed, birth weight, and litter size

To survive, the newborn lamb must be able to maintain body temperature and to stand and move to the udder to suck colostrum to fuel heat production. The objective of this study was to investigate whether neonatal lambs showing slow behavioral progress to standing and sucking also have an impaired ability to maintain body temperature. The time taken to stand and suck after birth, rectal temperatures, and blood samples were collected from 115 newborn single, twin, and triplet lambs of 2 breeds, Scottish Blackface and Suffolk, which are known to show variations in their neonatal behavioral progress. Blood samples were assayed for thyroid hormones, known to be involved in heat production, and cortisol, which plays a role in tissue maturation before birth. In addition, colostrum samples were collected from the 56 ewes that gave birth to the lambs, and assayed for protein, fat, and vitamin contents. Heavy lambs (more than 1 SD above the breed mean), Blackface lambs, and singleton or twin lambs were quicker to stand and suck from their mothers than lightweight (more than 1 SD below the breed mean), Suffolk, or triplet lambs. Low birth weight lambs also had lower rectal temperatures than heavier lambs (P < 0.01), as did Suffolk compared with Blackface lambs (P < 0.001). Lambs that were slow to suck after birth had lower rectal temperatures than quick lambs, and this difference persisted for at least 3 d after birth. Within breed, heavy lambs had greater plasma triiodothyronine and thyroxine immediately after birth than light lambs. Blackface lambs had greater plasma triiodothyronine and thyroxine than Suffolk lambs but tended to have less cortisol. Colostrum produced by Blackface ewes had a greater fat content than that of Suffolk ewes (P < 0.001). Thus, lambs that are behaviorally slow at birth are also less able to maintain their body temperature after birth. Although part of their lower body temperature might be attributable to behavioral influences on thermoregulation, the data also suggest that physiological differences exist between these animals. These differences may be related to different degrees of maturity at birth.     

Models with cytoplasmic effects for birth,weaning, and fleece weights,and litter size at birth for a population of Targhee sheep

Fifteen models were compared for the birth weight of 33,994 lambs recorded at the U.S. Sheep Experimental Station (1950 to 1998). The initial intent was to estimate fractions of variance due to cytoplasmic line (c2; n = 892) and sire by cytoplasmic line interaction (sc2; n = 17,557). The basic model included direct genetic (fractional variance, a2; n = 35,684), maternal genetic (m2, with correlation r-am), and maternal permanent environmental (p2; n = 8,418) effects. The model with sc2 was significantly better than the basic model with and without c2. When other random effects were added, sc2 became zero. Significant effects were associated with random dam x year (dy2; n = 24,801), sire x dam (sd2; n = 23,924), and dam x number born (dn2; n = 12,944) interaction effects. Estimates with all effects in the model were a2, 0.24; m2, 0.19; r-am, 0.11; p2, 0.05; c2, 0.00; dn2, 0.04; dy2, 0.06; sd2, 0.05; sc2, 0.00. Estimates for a2, m2, and r-am were the same for all models. Estimate of p2 changed when other effects were added to the model. Largest estimates for nongenetic effects were: p2, 0.08; c2, 0.00; dy2, 0.13; sd2, 0.11; and sc2, 0.04. Regardless of whether Westell groups (n = 91) were in the model, estimates were similar. For weaning weight (120-d, n = 32,715), estimates of variances of effects added to the basic model were all near zero (a2, 0.18; m2, 0.12; r-am, -0.01; p2, 0.06). For number born (NB, n = 37,020) and fleece weight (FW, n = 36,197), animal permanent environmental effects were added to the model (ap2; n = 9,871 and 9,760) and r-am was dropped. For these traits, effects not in the basic model had small variances. Nonzero estimates with full model were a2, 0.10; ap2, 0.01; dy2, 0.02; and sc2, 0.01 for NB, and a2, 0.54; m2, 0.02; ap2, 0.02; dy2, 0.04; and sc2, 0.02 for FW. Cytoplasmic effects were not important. The addition of unusual random effects to the model did not change estimates for the basic parameters. Although some of these effects were significant, especially for BW, the effects on genetic evaluations are likely to be small.     

Effect of birth and fraternal litter size and cross-fostering on growth and reproduction in swine

Twelve hundred fifty-one pigs from six farrowings (FGRP) were classified within a FGRP by their birth litter size (BL- = below average and BL+ = above average), randomly allotted to nursing litter sizes of 6 or 12+ pigs/sow (NL- vs NL+) and reared by their own or foster dams (XF- vs XF+). Pigs were weighed at birth, 21 d and when near 105 kg. A random sample of 40 gilts per FGRP was retained for observation of pubertal age and primipara conception. Twenty-four gilts per FGRP were farrowed and rebred for a second parity. Pigs born in large litters were younger at 105 kg than those born in small litters (189 vs 196 d +/- 1.4); no other differences (P greater than .05) were observed for BL. Pigs reared in larger litters had lower survival rate from birth to weaning (79 vs 86% +/- 1), had slower weight gains to 21 d of age (5.3 vs 6.6 kg +/- .17) and were older at 105 kg (195 vs 190 d +/- 1.4) than those reared in small litters (P less than .04). Cross-fostered pigs were slower gaining to 21 d (5.9 vs 6.1 kg +/- .14) and were older at 105 kg (195 vs 191 d +/- 1.4) than pigs not cross-fostered pigs (P less than .02). Growth beyond 105 kg and pubertal age were unaffected by any factor studied (P greater than .05). Although size of birth litter did not affect (P greater than .05) any reproductive trait, an interaction between litter size and farrowing group was detected.(ABSTRACT TRUNCATED AT 250 WORDS)     

Genetic analysis of litter size in Targhee, Suffolk, and Polypay sheep

Data on litter size, weaning weights at 60, 90, and 120 d, postweaning gains from weaning to 120 or 365 d of age, fleece weight, and fiber diameter from Targhee, Suffolk, and Polypay flocks participating in the U.S. National Sheep Improvement Program were used to estimate genetic parameters for litter size and genetic relationships between early-life traits and future litter size. Records on 7,591 lambings by 3,131 Targhee ewes, 10,295 lambings by 5,038 Suffolk ewes, and 6,061 lambings by 2,709 Polypay ewes were used. Heritability estimates for litter size ranged from .09 to .11 across breeds; repeatability ranged from .09 to .13. Additive genetic effects on litter size were generally positively, and occasionally significantly, correlated with animal additive genetic effects on weaning weights and postweaning gains. Genetic correlations (r(a)) ranged from .08 to .48 in Targhee and from .17 to .43 in Suffolk but were close to 0 in Polypay (-.14 to .09). Additive maternal effects on weaning weight were positively associated with litter size in Suffolk and Polypay; this correlation was negative (-.23 to -.35), but not significant, in Targhee. Fleece weight was not strongly associated with litter size; (r(a) = -.09 to .21). However, fiber diameter had a significant undesirable correlation with litter size (.30) in Targhee. Estimates of phenotypic correlations of litter size with early-life traits were uniformly small (-.02 to .08). Thus, although occasional genetic antagonisms between litter size and early-life traits were observed in these data, none appeared large enough to prevent simultaneous genetic improvement in both traits.     

Variance components and genetic parameters for weight and size at birth in the Boer goat

Variance components, heritability (direct additive and maternal) and correlations (additive genetic, phenotypic, maternal genetic and environmental) of body weight (BW) and body size including length (BL), height (BH) and chest girth (BCG) at birth in Boer goats were estimated on the basis of 5096 records obtained from a Boer Goat Breeding Station in Yidu, China, during 2001–2005. The parameters were estimated using a DFREML procedure by excluding or including maternal genetic or permanent maternal environmental effects, four different analysis models were fitted in order to determine the optimum model for each trait. The environmental factors such as year, season, sex and litter size (LS, number of kids) were investigated as the fixed effects. The results showed that the maternal effects were important determinants of estimated the genetic parameters for birth traits. Year and season had significant effect on birth traits. Single births and male kids had the heaviest live weight and the largest body size at birth. The mean values and standard deviation (SD) of BW, BL, BH and BCG were 3.87 ± 0.85 kg, 31.67 ± 2.87 cm, 32.92 ± 2.80 cm, 33.46 ± 3.21 cm. The mean values and standard error (SE) of direct additive heritability estimates for BW, BL, BH and BCG calculated with the optimum model were 0.19 ± 0.08, 0.14 ± 0.07, 0.24 ± 0.09 and 0.25 ± 0.10, respectively. For all the birth traits, estimates of the correlations between direct additive and maternal genetic (r_a–m) were negative. The estimates of additive genetic and phenotypic correlations among the birth traits were high and positive, and implied no genetic antagonisms among these traits analyzed. The estimates of maternal genetic correlations also were high and positive. Medium and positive environmental correlations indicated the important effects of environmental factors on early growth traits.     

Effect of selection for litter size and body weight on hormone-induced ovulation rate in mice.

Genetic differences in natural vs hormone-induced ovulation rates were compared in immature female mice from five lines that had undergone long-term single-trait and antagonistic index selection for litter size and(or) 6-wk BW. Lines used were control (K); high litter size (L+); high BW (W+); low litter size and high BW (L-W+); and high litter size and low BW (L+W-). Natural ovulation rate at a mean age of 34.3 d and hormone-induced (5 IU of pregnant mare's serum gonadotropin followed 2 d later by 5 IU of human chorionic gonadotropin) superovulation rate at a fixed age of 31 d were obtained. Total number of eggs ovulated was affected by line (P less than .001), treatment (P less than .001), and line x treatment interaction (P less than .001). Line differences were subsequently tested within treatment because of the significant line x treatment interaction. Line differences were important (P less than .001) for natural ovulation, hormone-induced ovulation, and response to hormones. Mean natural ovulation rates for K, L+, W+, L-W+, and L+W- were 14.1, 19.8, 15.1, 13.6, and 16.4, respectively. Selection changed ovulation rate by 40, 16, 7, and -4% in the L+, L+W-, W+ and L-W+ lines, respectively (P less than .01). Hormone-induced ovulation rates in K, L+, W+, L-W+, and L+W- were 32.3, 24.6, 19.6, 20.9, and 22.1, respectively. Exogenous hormones increased ovulation by 18.2, 4.8, 4.6, 7.3, and 5.7 ova for K, L+, W+, L-W+, and L+W-, respectively (P less than .001). Lines with lower natural ovulation rates had higher responses to superovulation. Increased ovulation rate due to treatment ranged from 24.3% in L+ to 129% in K. These results indicate significant differences among lines in ovarian response to exogenous hormones.     

Genetic and environmental influences on size of first litter in sheep, estimated by the REML method

Fixed effects of age at first litter and of season of lambing as well as variance components for additive genetic, flock × year and sire of litter effects on size of first litter were estimated for an animal model by a derivative-free REML procedure. Data of the four Swiss sheep breeds White Alpine (WAS), Brown-headed Meat (BFS), Black-Brown Mountain (SBS) and Valais Black Nose (SN) were available. Number of first litters used were 21 384, 21 607, 15 013, 12 394 and 18 110 the WAS (two data sets, WAS1, WAS2), BFS, SBS and SN, respectively. Litter size of ewes lambing the first time at 2 years of age was 0.27, 0.31, 0.41, 0.46 and 0.26 lambs larger than of ewes lambing the first time at 1 year of age. The largest increase occurred for the two breeds (BFS, SBS) with the lowest average age at first litter. The largest difference between any two lambing seasons within breed were 0.16, 0.16, 0.29, 0.22 and 0.07 lambs. Estimates of additive genetic variance of size of first litter were between 0.0269 (SN) and 0.0765 (SBS). Heritability estimates for this trait were 0.171, 0.156, 0.114, 0.225 and 0.122 for WAS1, WAS2, BFS, SBS and SN, respectively. A large flock × year component (relative to phenotypic variance) of 0.148 was found for SN, compared with estimates between 0.042 and 0.067 for the other breeds. A sire of litter component (relative to phenotypic variance) of 0.066 was found for SN, compared with estimates between 0.016 and 0.039 for the other breeds. It can be concluded that all nongenetic effects investigated should be taken into account for the estimation of additive genetic variance and breeding values for size of first litter, and that considerable variation in size of genetic and nongenetic effects exists in the sheep breeds under consideration.     

Influence of management system on litter size, lamb growth, and carcass characteristics in sheep.

Three management systems (winter, spring, and late summer) distinguished by season of lambing and management practices were compared for litter size born and weaned and growth and carcass characteristics of lambs. Three sire breeds (Cheviot, Rambouillet, and Suffolk) and three dam breeds (Florida Native, Native-X, and Synthetic-X) were used in 698 matings over a 3-yr period. System affected (P < .01) litter size born. Spring lambing yielded more lambs (1.62) than winter (1.49) and late summer (1.12). The winter-born lambs were lighter but fatter (P < .05), and spring-born lambs were leaner with higher leg conformation and carcass quality scores. The late summer-born lambs were not different from spring-born lambs. Wethers had higher (P < .01) weights off test than ewe lambs (43.9 vs 42 kg) but had lower (P < .01) leg conformation scores, percentage kidney and pelvic fat, yield grade, and dressing percentages. Dam breed effects were significant (P < .05) for average preweaning daily gains with 249+/-5, 201+/-9, and 191+/-9 g for progeny of Native-X, Florida Native, and Synthetic-X, respectively. Single-born lambs had higher daily gains (P < .05) than twins in a preweaning period in all management systems and higher postweaning and lifetime daily gains for winter and spring management systems.     

Effect of season and outdoor climate on litter size at birth in purebred landrace and yorkshire sows in Thailand

The objective of the present study was to retrospectively investigate causes of variation on litter size at birth (total number of piglets born per litter (TB) and number of piglets born alive per litter (BA)) of Landrace (L) and Yorkshire (Y) sows in swine nucleus herds in Thailand. The data included sows farrowed during a four-year period from January 1998 to December 2001. The analyzed data set included observations on 8020 litters from 2199 L sows and 6919 litters from 1680 Y sows. Analysis of variance (ANOVA) was applied for statistical analyses using General Linear Mixed Model (MIXED) procedure of SAS. No breed difference was found for both TB and BA. Farrowing months significantly influenced TB and BA (P<0.001). Sows farrowed in August and September had a lower BA than sows farrowed from November to June (P<0.05). Effect of farrowing months on both TB and BA was more pronounced in primiparous compared with multiparous sows. Average minimum daily temperature during gestation negatively correlated with both TB and BA, average maximum daily temperature during gestation negatively correlated with BA and average daily humidity during gestation negatively correlated with both TB and BA. The correlations were stronger in L than in Y sows.