Characterization of straightbred and crossbred rabbits for milk production and associative traits

Two hundred twenty-five lactation and litter performance records from 82 does representing four genetic groups and two diets were analyzed to quantify breed, heterosis, reciprocal F1 cross and diet effects for milk production and associative traits. Doe genetic groups were New Zealand White (NN) and Californian (CC) straightbred and Californian X New Zealand White (CN) and New Zealand White X Californian (NC) reciprocal crossbreds. Pelleted diets fed to does and litters were either a commercial control or a 74% alfalfa diet. Three sire breeds of litters included NN, CC and Flemish Giant (FG) straightbreds. Doe genetic group and diet were important sources of variation (P less than .05) for all traits examined except for litter milk efficiency (litter gain/milk intake) and doe feed efficiency (milk yield/feed intake). The sire breed of litter effect did not influence (P greater than .05) lactational performance of does nor associative preweaning traits. Straightbred NN does were heavier at kindling, yielded more milk, reared a heavier litter by 21 d and were more efficient in converting feed into milk than were straightbred CC does (P less than .01). Significant heterosis was detected for milk production and for litter size and weight at 21 d. Reciprocal differences between crossbred doe groups were observed (P less than .05) for litter milk efficiency and doe feed intake. The 74% alfalfa diet was superior to the commercial control diet for effects on milk production and litter size and weight at 21 d, although doe feed intake was increased.(ABSTRACT TRUNCATED AT 250 WORDS)     

Prediction and causation of litter market traits from preweaning and weaning characteristics in commercial meat rabbits

Market data on 1,315 rabbits from 201 litters from Californian (CAL), New Zealand White (NZW), CAL X NZW and NZW X CAL dams bred to CAL, NZW and Flemish Giant sires were subjected to multiple regression and path analyses. Market traits observed in litters at 56 d included average kit weight (A56W), litter size (LS56), total litter weight (L56W) and within-litter uniformity in individual weights (LCV). Preweaning variables as covariates included in the model were dam metabolic body weight (DMW), litter born (LSB), litter birth weight (LBW), milk yield from 1 to 21 d (MY) and feed intake from 1 to 28 d of the dam and litter (FI). Results from multiple regression analyses indicated linear and quadratic effects (P less than .20) due to LSB and MY for all four market characters. The LBW influenced (P less than .05) LS56 and L56W, and FI affected (P less than .05) LS56, L56W and LCV. Separate analyses were conducted involving 28-d weaning and feed intake variables as covariates: litter size weaned (LSW), litter weaning weight (LWW) and litter feed intake from 28 to 56 d (LFI). The three weaning covariates were important (P less than .05) for all market traits except LS56 (LWW was not significant). The most accurate regression equations were obtained from the weaning model for prediction of L56W and LS56 (R2 = .68 and .78). Path analyses revealed that preweaning covariates generally had direct rather than indirect effects on market traits. Both direct and indirect effects of weaning covariates were important for market traits. Results suggest that litter market traits of size and weight can be predicted with a reasonable degree of accuracy.     

Performance of mouse lines divergently selected for heat loss when exposed to different environmental temperatures. I. Reproductive performance, pup survival, and metabolic hormones

Mouse populations differing in metabolic rate have been developed through selection for high (MH) and low (ML) heat loss, along with the unselected controls (MC). Objectives of the study were to compare the MH, ML, and MC lines for reproductive performance, pup survival, and metabolic hormones when reared at 12, 22, and 31 degrees C, and to search for line x environment interactions. Conception and litter size were recorded on the parent generation mice introduced to the environments at 11 wk of age and bred after a 3-wk acclimatization period. Survival of pups (preweaning to 3 wk; postweaning from 3 to 9 wk of age) was measured with continuous exposure in the designated environment from birth to the time of measurement. Corticosterone, triiodothyronine (T3), and thyroxine (T4) serum concentrations were measured on the parent generation after producing litters and on the pup generation at 9 wk. No line x environment interaction was detected for conception rate, preweaning mortality, postweaning survival, pup weaning weight, or body temperature. There were no differences in conception rate among lines and environments. Environments affected survival of pups, but there were no line differences. Rectal body temperatures were greater for MH than ML mice, and MC mice were intermediate; body temperature of mice did not differ among the environments. Lines differed significantly in litter size only in the 22 degrees C environment. No significant line differences were found for serum corticosterone or serum T3 or T4. Line x environment interaction was detected only for litter size and for serum corticosterone concentration in dams. Contrary to the other two lines, ML dam performance relative to MH and MC was not affected negatively by either of the thermal environments. Results from this study do not raise concern that selection to decrease maintenance requirements will produce livestock with any greater liability to cope and perform under an array of environmental temperatures.     

Energy intake and milk production in mink (Mustela vison)--effect of litter size.

Energy intake and milk production were measured in 12 mink dams raising litters of 3, 6 and 9 kits one to four weeks post partum by means of balance experiments and measurements of milk intake of the kits by the water isotope dilution technique. The dams were fed ad libitum on a conventional wet mink diet (DM: 323 g/kg; CP: 173 g/kg; ME: 4.4 MJ/kg). Milk samples collected from dams with corresponding litter sizes and lactation weeks, and body composition of kits nursed by these dams, were analysed for content of DM, ash, N and fat. The ME and drinking water consumption were higher in dams nursing 9 kits than in dams nursing 3 kits. The N and water balances as well as the live weight of dams were not affected by litter size. Daily milk production was higher in dams nursing 9 kits than in dams nursing 3 kits. The DM, N and fat content of the milk increased during lactation, but were not affected by litter size. Individual kit live weight was higher in litters of 3 than in litters of 6 and 9 kits four weeks post partum. The DM and fat content of the kits were lowest in kits from litters of 9 kits, whereas these kits had the highest protein content. Daily ME for maintenance of kits and the efficiency of utilisation of ME in milk for body gain were estimated to 356 kJ/kg0.75, kp approximately 0.53 and kf approximately 0.71, respectively. In conclusion, daily milk production increased with increasing litter size, but not in proportion to the number of kits, indicating that milk production limits the growth rate of the young. In the fourth week of lactation, milk production was not different between dams nursing 6 or 9 kits, indicating a maximum capacity.     

Comparison of feed energy costs of maintenance, lean deposition, and fat deposition in three lines of mice selected for heat loss

Three replications of mouse selection populations for high heat loss (MH), low heat loss (ML), and a nonselected control (MC) were used to estimate the feed energy costs of maintenance and gain and to test whether selection had changed these costs. At 21 and 49 d of age, mice were weighed and subjected to dual x-ray densitometry measurement for prediction of body composition. At 21 d, mice were randomly assigned to an ad libitum, an 80% of ad libitum, or a 60% of ad libitum feeding group for 28-d collection of individual feed intake. Data were analyzed using 3 approaches. The first approach was an attempt to partition energy intake between costs for maintenance, fat deposition, and lean deposition for each replicate, sex, and line by multiple regression of feed intake on the sum of daily metabolic weight (kg(0.75)), fat gain, and lean gain. Approach II was a less restrictive attempt to partition energy intake between costs for maintenance and total gain for each replicate, sex, and line by multiple regression of feed intake on the sum of daily metabolic weight and total gain. Approach III used multiple regression on the entire data set with pooled regressions on fat and lean gains, and subclass regressions for maintenance. Contrasts were conducted to test the effect of selection (MH - ML) and asymmetry of selection [(MH + ML)/2 - MC] for the various energy costs. In approach I, there were no differences between lines for costs of maintenance, fat deposition, or protein deposition, but we question our ability to estimate these accurately. In approach II, selection changed both cost of maintenance (P = 0.03) and gain (P = 0.05); MH mice had greater per unit costs than ML mice for both. Asymmetry of the selection response was found in approach II for the cost of maintenance (P = 0.06). In approach III, the effect of selection (P < 0.01) contributed to differences in the maintenance cost, but asymmetry of selection (P > 0.17) was not evident. Sex effects were found for the cost of fat deposition (P = 0.02) in approach I and the cost of gain (P = 0.001) in approach II; females had a greater cost per unit than males. When costs per unit of fat and per unit of lean gain were assumed to be the same for both sexes (approach III), females had a somewhat greater estimate for maintenance cost (P = 0.10). We conclude that selection for heat loss has changed the costs for maintenance per unit size but probably not the costs for gain.     

Comparison of rabbit breed types for postweaning litter growth, feed efficiency, and survival performance traits

Postweaning data on 643 rabbits from 122 litters representing four breed types, New Zealand White (NZW) and Californian (CAL) purebreds, CAL X NZW (CXN), and Flemish Giant (FG) crossbreds (the latter group was a collection of FG X CAL, FG X Champagne D'Argent [CHA], and 1/2 FG X 1/4 CAL X 1/4 CHA), were gathered over five seasons and compared for growth, feed efficiency, and survival-related performance traits. Evaluation criteria included litter size and weight at weaning (28 d); 28- to 70-d litter feed intake, weight gain, feed efficiency, and mortality rate; and litter and average market weight (70 d). The least squares model included main effects of breed type, season of birth of the litter and parity of dam, litter size at weaning as a linear covariate, and the random error. Breed-type differences were not detected for litter size and weight at weaning and feed efficiency. Purebred NZW and CAL litter trait performances were comparable (P greater than .05). Purebred NZW litters consumed less feed than CXN and FG crosses, gained weight less rapidly than FG crosses, and weighed less per fryer at 70 d than CXN and FG crosses (P less than .05). Feed intake was lower and average market weight was lighter for CAL purebred litters than for CXN and FG crossbred litters (P less than .05). The CXN and FG crossbreds only differed (P less than .05) for average market weight (2,078 vs 2,192 g). Mortality rate was lower (P less than .05) in CXN crossbred litters than in CAL purebred litters.(ABSTRACT TRUNCATED AT 250 WORDS)     

Age of cow and age of dam effects on milk production of Hereford cows

Milk production in Hereford cows was studied utilizing 2,487 lactation records on 926 cows. Data were collected over 17 yr (1968 to 1984) from two related herds. Estimates of daily milk yield were obtained at bimonthly intervals by the calf suckling technique. The sum of three monthly measures (TMY), a predicted sum of seven monthly observations (PMY) and 205-d weight of the calf were studied. Year, age of cow, age of dam at cow's birth and calf birth weight affected (P less than .05) all traits. Birth weight affected all measures of milk, with heavier calves obtaining more milk. Age of cow effects were significantly curvilinear, with PMY and TMY increasing for cows from 2 to 5 yr of age, but not differing for cows 6 yr and older. Age of cow effects on 205-d weight were similar to those for milk. As age of cow increased from 2 to 4 yr, 205-d calf weight increased. A leveling off in 205-d weight was observed for calves of cows 5 yr and older. Effects of age of dam of cow also were significant for all milk traits studied. As age of dam increased, PMY and TMY decreased. Highest milk yields were for cows born to and reared by 2-yr-old dams, intermediate milk yields for those by 3- and 4-yr-old dams and lowest yields by daughters of mature dams. Cows born to and reared by older dams produced less milk and weaned lighter calves. There were no interactions between age of cow and age of dam. This suggests a lasting detrimental effect of older cows on lactation yield of daughters. Thus, it appears that age of dam should be considered in evaluation of cow performance.     

Lactational performance of first-parity transgenic gilts expressing bovine alpha-lactalbumin in their milk

The goal of this study was to determine whether the presence of the bovine alpha-lactalbumin transgene in first-lactation gilts enhances lactational performance and litter growth. Transgenic and sibling nontransgenic gilts were bred to nontransgenic boars. Litters were standardized to 10 piglets within 24 h of farrowing. Milk production was measured by the weigh-suckle-weigh method on d 3, 6, 9, and 12 of lactation. Bovine alpha-lactalbumin was present in the colostrum and milk of transgenic gilts throughout lactation. The expression of the transgene was associated with alterations in composition of mammary secretions, especially in early lactation. Lactose concentrations were greater (P < 0.05) in mammary secretions of transgenic gilts during the first 12 h postpartum compared with controls. In contrast, total solids concentration in mammary secretions from transgenic gilts were lower (P < 0.05) relative to controls during the first 6 h postpartum. Transgenic gilts produced more milk than controls on d 3, 6, and 9 of lactation (P < 0.01). By d 12, differences in milk production between transgenic and control sows were no longer different. Lactose intake by transgenic-reared litters was greater than lactose intake by control-reared litters on d 6 of lactation (P < 0.05). Total solids intake was significantly greater (P < 0.05) by transgenic-reared litters on d 3 and 6 compared to control-reared litters. The day x genotype interaction on litter weight gain after birth was highly significant (P = 0.011), with transgenic-reared litters gaining weight at a greater rate than control-reared piglets. Expression of the transgene was associated with increased milk production in lactating gilts and increased growth of transgenic-reared piglets. Increased lactose synthesis in response to the presence of the transgene may result in increased milk production in early lactation, leading to increased milk component intake by transgenic litters, and ultimately to increased growth of litters reared by first-parity transgenic gilts.     

Reallocation of body resources in lactating mice highly selected for litter size

The present study investigated differences in the allocation patterns of body stores in lactating female mice from a line selected for high litter size at birth (S-line, average litter size of 20) and dams from a nonselected control line (C-line, average litter size of 10). Body weight, litter size, litter weight, and absolute and relative lipid and protein mass were measured at peak lactation (2 wk in lactation) and at weaning (3 wk in lactation). Body size in S-line females has been increased as a correlated effect of selection for high litter size at birth, allowing for larger litters and higher absolute milk production. However, these dams produce larger litters relative to their own body weight. At peak lactation, lipid and protein percentage did not differ between lines. At weaning, S-line females had a higher protein percentage (P < 0.001) and lower lipid percentage (P < 0.05) than C-line females. Apparently, S-line females produce more offspring but at a greater cost to their own metabolism. This process was insufficient to supply the offspring with adequate resources, resulting in reduced (P < 0.0001) pup development and increased (P < 0.0001) preweaning mortality rates.     

Direct and maternal genetic differences between lines of mice selected for body weight and litter size: traits of dams

Genetic differences in performance of dams were estimated by linear contrasts using means of two selected lines of mice and reciprocal F1's, F2's and backcrosses. The lines were selected for increased 6-wk body weight (W) or increased litter size (L). Genetic differences estimated were direct average (gD), direct heterosis (hD), maternal average (gM), progeny average (gP), and progeny heterosis (hP). For dam weight and feed consumption from 12 to 21 d postpartum (pp), gD was the largest genetic difference and favored line W. For litter size, litter weight at birth, litter efficiency (litter weight gain/dam feed consumption) from birth to 12 d pp and within litter mortality from 1 to 21 d pp, gD favored L and, except for hD in litter efficiency, was the most important genetic difference for these traits. Direct heterosis was the only significant difference for litter weight at 21 d pp, litter efficiency from 12 to 21 d pp and within litter mortality at parturition. The gM were larger in W than in L for dam weight and feed consumption, and for litter size and weight at birth, but they were usually of smaller magnitude than gD. The gP were significant only in litter traits measured before 12 d pp and favored W. For no trait measured was hP of consequence. Line differences in dam and litter weight accounted for genetic differences in dam feed consumption. Genetic differences in litter size at birth were not due to line differences in dam weight. The lower mortality within litters nursed by crossbred dams was responsible for hD on litter weight and litter efficiency. Within but not among lines, higher mortality rates were associated with larger litters.     

Renewed selection for heat loss in mice: direct responses and correlated responses in feed intake, body weight, litter size, and conception rate

Divergent selection in mice was renewed in 3 independent replicates for high (MH) and low (ML) heat loss. An unselected control (MC) was maintained in all replicates. Heat loss was measured for individual male mice for 15 h, overnight in direct calorimeters. After 16 initial generations of selection followed by 26 generations of relaxed selection, divergent selection resumed for 9 generations. The realized selection applied was very close to the maximum possible selection according to the criteria and protocol. Selection differentials were greater for high than for low selection due to greater variation in the MH line. When corrected for SD, standardized selection differentials were similar for MH and ML selection. Unintended selection in MC was negligible. Realized heritability for divergence was 0.14 +/- 0.01, which was considerably less than that realized during the initial generations of selection (0.28 +/- 0.03). Realized heritabilities for MH selection (0.16 +/- 0.05) and for ML selection (0.07 +/- 0.06) were less, especially for ML selection, than were observed in the earlier generations. The difference in heat loss between MH and ML males was 55.7% of the MC mean at generation 51, compared with a difference of 53.6% in generation 15; this difference had decreased to 34.4% at the end of the relaxed selection (generation 42). For feed intake between 8 and 11 wk, MH and ML males differed by 34.0% of the MC mean by the end of the selection process. Body weight at 12 wk for MH and ML males was less than for MC males. Litter size response was positively related to the heat loss response. Conception rate was poorer in MH matings than in MC and ML matings.     

Heterosis and recombination effects in Hampshire and Landrace swine: I. Maternal traits.

Hampshire and Landrace sows and crossbreds of the two breeds were used to determine heterosis and recombination effects for milk production, milk composition, and litter traits at birth and d 21. Twelve mating types were represented in this study: two purebred, two F1, two F2, two F3, and four backcross. Information was gathered on a total of 358 litters over four farrowing seasons. Milk production was measured at d 10 and 20 of litter age according to the weigh-suckle-weigh procedure. Milk samples were collected at d 10 and 20 of litter age and evaluated for percentages of fat (PCFA), protein (PCPR), lactose (PCLA), and solids-not-fat (PCSN). The model used to evaluate litter traits at birth included main effects of mating type, parity, and farrowing season. The model used for milk production and milk composition traits included these main effects and number of pigs nursed as a covariate. Estimates of maternal genetic effects showed that Landrace females were superior to Hampshire females for number born (NB), number born alive (NBA), litter birth weight (LBW), adjusted 21-d litter weight (ALW), and milk production at d 10 of litter age (WT10). Hampshires were superior to Landrace for PCPR at d 10 of litter age and PCSN at d 10 and 20 of litter age. Heterosis effects were significant (P less than .05) for NBA (.97) and LBW (1.46 kg). Maternal heterosis effects were significant for LBW (3.94 kg; P less than .01). Epistatic recombination losses in the offspring were significant for LBW (6.80 kg; P less than .05). Differences in maternal performance of reciprocal F1 dams were generally not significant. Heterosis and recombination effects were not significant for milk production or milk composition.     

Performance of mouse lines divergently selected for heat loss when exposed to different environmental temperatures. II. Feed intake, growth, fatness, and body organs

Mouse populations differing in metabolic rate have been developed through selection for high (MH) and low (ML) heat loss, along with the unselected controls (MC). Objectives of the study were to compare the MH, ML, and MC lines for feed intake, growth, body fatness, and organ weights when reared at 12, 22, and 31 degrees C, and investigate potential line x environment interactions. Feed intake was recorded weekly from 3 to 9 wk of age, and BW at 3, 6, and 9 wk of age. Body fat percent and organ weights were measured at 9 wk of age. No line x environment interactions were detected for any of the traits measured. The MH mice consumed more feed than ML mice from 5 to 9 wk of age. Between 8 and 9 wk of age, MH mice consumed 13% more feed than the ML mice, but they were relatively leaner (14.45 vs. 16.32% body fat); MC mice were intermediate for both traits. Mice in the cold environment consumed the greatest amount of feed, and those in the hot environment consumed the least. Males consumed more feed than females, and the difference was greater in the cold than in the hot environment. No differences in BW were found between the lines. Mice in the 22 degrees C environment were heavier than their age-matched counterparts in the other two environments, and males were heavier than females at all ages. Relative to BW, the three lines had similar tail length, body length, and liver weight. Mice in the cold environment had heavier spleens and livers than those in the hot environment but relatively shorter bodies and tails; the normal environment was intermediate for these traits. Results from this study indicate that selection to decrease maintenance requirements did not produce mice with any less ability to grow and perform under an array of environmental temperatures.     

品种对肉兔断奶后窝生长性状的影响

本研究旨在明确影响肉兔断奶后窝生长性状和料肉比的重要因素。利用一般线性模型分析了来自5个不同肉兔品种(新西兰白兔,加利福尼亚兔,比利时兔,青紫蓝兔和福建黄兔)的909只173窝肉兔断奶后窝生长和料肉比性状。结果表明,品种和断奶数对断奶窝重(5周龄窝重),窝增重,窝上市体重(10周龄窝重),个体平均上市体重,窝采食量和料肉比的影响极显著(P<0.01)。出生月份对窝采食量影响极显著(P<0.01),对断奶窝重和窝上市体重的影响显著(P<0.05)。比利时兔的断奶窝重、窝增重、窝上市体重、窝采食量和平均上市体重显著高于其他品种,而福建黄兔的上述5项指标显著低于其他品种(P<0.05)。断奶数与断奶窝重、窝采食量、窝增重、窝上市体重和料肉比的回归系数为正且显著。品种、断奶数和出生月份是影响肉兔断奶后窝性状和料肉比的重要因素。本研究的结果为将比利时兔作为杂交的终端父本提供重要依据。     

Traits affecting postweaning weight gain and feed intake of primiparous sows

Seventy-six primiparous Duroc and Landrace sows from two genetic lines with or without selection for improved sow productivity were used to identify sow traits that affect postweaning gain (positive or negative) and feed intake. Sows lost weight (P less than .01) and consumed less feed (P less than .01) during wk 1 postweaning (37 d) compared with wk 2, 3, and 4. Sows gained more weight during wk 2 and 3 (P less than .01) than during wk 4. Weekly feed consumption was similar during wk 2 and 4 and highest during wk 3 (P less than .05). Sow weight gain postweaning was predicted by sow weaning weight (P less than .01) and adjusted 21-d litter weight (P less than .05) during wk 1, wk 1 to 2, and wk 1 to 4 feeding periods. Feed consumption was best predicted by adjusted litter weaning weight (P less than .01), sow weaning weight (P less than .01), average backfat at farrowing (P less than .01), average backfat change (P less than .05), and adjusted 21-d litter weight (P less than .05). Feed intake was positively correlated (P less than .01; r = .77) and sow weight at breeding, farrowing, and weaning was negatively correlated (P less than .05; r = -.23, -.21, and -.26, respectively) with sow weight gain. Average backfat at weaning was negatively correlated (P less than .05) with gain and feed intake during each period. Adjusted 21-d litter weight and adjusted litter weaning weight were positively correlated with postweaning feed intake (P less than .05; r = .22 and .23, respectively).(ABSTRACT TRUNCATED AT 250 WORDS)     

Locomotor activity, core body temperature, and circadian rhythms in mice selected for high or low heat loss

Daily locomotor activity, core body temperature, and their circadian rhythms were measured in lines of mice selected for high (MH) or low (ML) heat loss and unselected controls (MC). Lines were created by selecting for 16 generations in each of three replicates. Collection of locomotor activity and core temperature data spanned Generations 20 and 21 for a total of 352 mice. Physical activity and core body temperature data were accumulated using implanted transmitters and continuous automated collection. Measurement for each animal was for 3 d. Activity was recorded for each half hour and then averaged for the day; temperature was averaged daily; circadian rhythm was expressed in 12-h (light vs dark) or 6-h periods as well as by fitting cyclic models. Activity means were transformed to log base 2 to lessen heterogeneity of variance within lines. Heat loss for a 15-h period beginning at 1630 and feed intake for 7 d were measured on 74 additional mice in order to estimate the relationship between locomotor activity and heat loss or feed intake. Selection lines were different (P < 0.01) for both locomotor activity and core body temperature. Differences were due to selection (MH-ML, P < 0.01), and there was no evidence of asymmetry of response (P > 0.38). Retransformed from log base 2 to the scale of measurement, mean activity counts were 308, 210, and 150 for MH, MC, and ML, respectively. Mean core temperatures were 37.2, 36.9, and 36.7 degrees C for MH, MC, and ML (P < 0.01), respectively. Females had greater physical activity (P < 0.01) and body temperature (P < 0.01) than males. There was no evidence of a sex x selection criterion interaction for either activity or temperature (P > 0.20). Overall phenotypic correlation between body temperature and log base 2 activity was 0.43 (P < 0.01). Periods during the day were different for both 12- and 6-h analyses (P < 0.01), but there were no period x selection criterion interactions (P > 0.1) for physical activity or body temperature. More sensitive cyclic models revealed significant (P < 0.01) 24-, 12-, 8-, and 6-h cycles that differed (P < 0.01) among lines. Estimated differences between MH and ML mice in feed intake and heat loss due to locomotor activity were 36 and 11.5%, respectively. Variation in activity thus contributed to variation in feed intake.     

Improving sow efficiency by management to enhance opportunity for nutritional intake by neonatal piglets

Starvation, primarily during the first week postpartum, is the direct or indirect cause of at least one-half of preweaning mortalities in healthy herds. Causes of starvation originate from characteristics of the dam, of the litter and of individual piglets. A major cause of starvation is congenital weakness associated with birth weights less than 1000 g. Increasing energy during late gestation shows inconsistent effects on birth weight; some dietary component energy sources appear to improve stamina of newborn and(or) energy content of sow's milk with favorable effects on survival. Total or partial supplemental nutrient intake supplied by caretakers, automated feeding devices or transfer of piglets to foster dams are the primary means of providing enhanced nutrient intake opportunity. Nutrient intake from non-dam sources ranges from temporary tube-feeding, administered by caretakers to excessively small or weak pigs, to self-feeding by pigs from simple or sophisticated dispensers of sow milk substitutes. Transfer of piglets to foster dams as a nutrient intake source is most successful when characteristics such as size of dam, size of teats, stage of lactation and temperament are in harmony with characteristics affecting pigs' needs. If other dams are not available, sows 2 to 3 wk into lactation can serve as foster dams for large and strong newborn piglets after resident litters are removed. Planning for availability of appropriate foster dams, based on prior or projected prolificacy and other sow and litter traits, should be done at time of assembling each mating group. Research results show that, on a weight-to-weight basis, pigs requiring artificial or foster dam rearing perform similarly to other pigs and thus justify management to secure their survival.     

Selection for postweaning gain in rats: III. Correlated response in maternal performance

Effects from 34 generations of selection, either up (U) or down (D), for 3- to 9-wk weight gain on genetic direct and postnatal maternal effects, dam size and maternal efficiency were evaluated in 25 cross-fostered sets of rats. Direct genetic effects on 12-d pup weight were 14 and 9% above controls (C) for U and D lines, respectively (P less than .01). Postnatal maternal effects on 12-d pup weight were also 11% higher for the U line (P less than .01), but not different from C for the D line. Females of the U line were heavier (P less than .01) by 13% at mating, 12% at parturition and 15% at 12 d of lactation, relative to controls. They also produced 11% greater total litter weight at 12 d and consumed 9% more feed, but were only nonsignificantly lower in feed per unit of pup 12-d litter weight. Females of D line were -8, -7 and -3% relative to controls in the three weights, but did not differ from controls in 12-d litter weight, feed consumed or in feed efficiency during lactation.     

The National Pork Producers Council Maternal Line National Genetic Evaluation Program: a comparison of six maternal genetic lines for female productivity measures over four parities

Litter (n = 8,424) and female performance records were collected in two breed-to-wean production units in order to evaluate genetic line differences for sow longevity and maternal performance over four parities. Lines evaluated were American Diamond Genetics, Danbred North America, Dekalb-Monsanto DK44, Dekalb-Monsanto GPK347, Newsham Hybrids, and National Swine Registry. Females within a line were derived from a minimum of 65 sires, 197 dams (three dams per sire), and a maximum of three daughters per dam, except in the GPK347, which were produced using semen from 12 Nebraska Index boars mated with Dekalb-Monsanto Line 34 females. All lines expressed 100% maternal heterosis. Mixed model statistical procedures were used with fixed effects including genetic line, parity, production unit, and two-way interactions. Random effects included a contemporary week of production and female for repeated records. Lactation length (average 15 d) was included as a linear covariate where appropriate. In total, 3,599 females entered as early-weaned pigs, 3,283 entered the breeding herd, 2,592 farrowed at least a single litter, and 1,656 and completed four parities. Line (P < 0.001) and parity (P < 0.001) effects were observed for virtually all traits measured. Ranges of genetic line differences averaged across parities were 1.76 pigs for total born, 1.45 pigs born alive, and 0.31 stillborn pigs per litter. Ranges of line differences in total and live litter weight were 1.4 and 1.3 kg, respectively. Ranges among lines, within Parities 1 through 4, for litter size at weaning were 0.56, 1.08, 0.91, and 0.64 pigs per litter, respectively. Line differences for weight (33.8 kg) and backfat depth (6.4 mm) at farrowing, lactation feed intake (8.7 kg), weight loss (5.0 kg), and backfat loss (0.87 mm) were observed. Extended wean-to-estrus interval was related to variation in weight, feed intake, and backfat loss in all lines except the GPK347. The GPK347 females farrowed and weaned the largest number of pigs, ate less feed in lactation, and lost more backfat and weight during lactation, yet they had the largest litters and the shortest wean-to-estrus intervals. Line x parity interactions existed for many traits due to small rank changes, but in general, the high- and low-ranked lines did not change. Genetic line differences in reproductive efficiency through four parities exist and must be recognized when choosing a female line.     

Genetic parameters and predicted selection results for maternal traits related to lactation efficiency in sows

The increased productivity of sows increases the risk of a more pronounced negative energy balance during lactation. One possibility to prevent this is to increase the lactation efficiency (LE) genetically and thereby increase milk output for a given feed intake and mobilization of body tissue. The benefits of selection for LE depend on its heritability and the relationships with other traits of interest. The objectives of this study were to estimate genetic parameters for LE, its underlying traits, and to predict the consequences of current selection strategies in dam lines. Data from 4 farms were available to estimate genetic parameters. Heritabilities were estimated by using a univariate repeatability model, and genetic correlations were estimated bivariately. Selection index theory was used to predict the genetic progress by 3 alternative breeding programs: 1) a breeding program that aimed at balanced progress in the total number of piglets born, piglet mortality, and percent prolonged interval from weaning to estrus; 2) extension of this breeding goal with LE; and 3) a breeding goal that included only one selection criterion, litter weight gain, to demonstrate the effect of indirect selection for milk production. The heritability for LE was low (0.12). Body fat mass (0.52) and BW (0.45) of sows at the beginning of lactation showed the greatest heritabilities. Protein mass at the beginning of lactation, protein loss, weight loss, and ad libitum feed intake during lactation showed moderate heritabilities (0.39, 0.21, 0.20, and 0.30, respectively). Low to moderate heritabilities were found for litter weight at birth, within-litter SD in the birth weight of piglets, litter weight gain, fat loss, and restricted feed intake during lactation (0.19, 0.09, 0.18, 0.05, and 0.14, respectively). Within-litter SD in the weaning weight of piglets showed no genetic variability. It was predicted that a breeding goal for dam lines with an emphasis on the total number of piglets born, piglet mortality, and percent prolonged interval from weaning to estrus would not dramatically change BW or body composition at the beginning of lactation, or mobilization of body tissue and feed intake during lactation. Inclusion of LE in the breeding goal will improve stayability, as defined by the first-litter survival of sows and LE itself, without negative consequences for other economically important traits. Nevertheless, it might be worthwhile to design a breeding goal in which LE increases and feed intake remains unchanged.