Genetic parameters of growth curve parameters in male and female chickens.

1. Individual growth curves of 7143 chickens selected for the form of the growth curve were fitted using the Laird form of the Gompertz function, BW4=BW0xe(L/K)(1-e-Kt) where BWt is the body weight at age t, BW0 the estimated hatching weight, L the initial specific growth rate and K the maturation rate. 2. Line and sex effects were significant for each parameter of the growth curve. In males, L, BW0, age and body weight at inflection (T(I)and BWI) were higher whereas K was lower than in females. Lines selected for high adult body weight had higher BW0 and BW(I) whereas lines selected for high juvenile body weight had larger estimates of L and lower estimates of T(I). 3. Data from 38,474 animals were included in order to estimate the genetic parameters of growth curve parameters in males and females, considering them as sex-limited traits. Genetic parameters were estimated with REML (REstricted Maximum Likelihood) and an animal model. Maternal genetic effects were also included. 4. Heritabilities of the growth curve parameters were moderate to high and ranged between 0.31 and 0.54, L, BW0 in both sexes and BW(I) in males exhibited significant maternal heritability. Heritabilities differed between males and females for BWI and T(I). Genetic correlations between sexes differed significantly from one for all parameters. L, K and T(I) were highly correlated but correlations involving BW0 and BW(I) were low to moderate. 5. Sexual dimorphism of body weight at 8 and 36 weeks and of L, K and T(I) was moderately heritable. Selection on growth curve parameters could modify the difference between sexes in precocity and thus in body weight at a given age.     

Genetic analysis of growth curve parameters for male and female chickens resulting from selection on shape of growth curve

The objectives of this research were to evaluate gender differences and selection on body weight as they affect growth curves of chickens. Marginal posterior densities of growth curve parameters were studied by Gibbs sampling on 10,671 male and female chickens originating from five lines. Line X-+ was selected on low body weight at 8 wk (BW8) and high body weight at 36 wk (BW36), line X+- on high BW8 and low BW36, X++ on high BW8 and BW36, X-- on low BW8, and BW36, and X00 was an unselected control line. Growth was modeled by a Gompertz function. Heritabilities and genetic correlations among parameters of the Gompertz curve were estimated. Marginal posterior densities were drawn for parameters of the growth curve and for sexual dimorphism at ages ranging from hatching to 1 yr. Lines selected for a higher BW8 had higher initial specific growth rates (L), higher maturation rates (K), and lower ages at inflection (T(I)). Lines selected for a higher BW36 had higher asymptotic body weights (A). Estimates of A, L, and T(I) were higher in males and K was higher in females. Difference between sexes for A was greater in the line selected for a lower BW8 and a higher BW36. Dimorphism for L and K was the lowest in lines X++ and X--, respectively. The greatest difference in T(I) was observed in the line selected for lower BW8 and BW36. Sexual dimorphism of body weight was lower at most ages in the lightest line. Before 15 wk, sexual dimorphism in X++ line was lower than in the line selected for higher BW8 and lower BW36. The increase in sexual dimorphism with body weight could be reduced by selecting animals on body weight at two ages instead of one, as is usually done in commercial lines.     

Postpartum performance in a diallel cross among lines of mice selected for litter size and body weight

Postpartum dam performance was studied in a complete diallel design involving five lines of mice. The selection criterion in each line was: large litter size at birth (L+); large 6-wk body weight (W+); an index for large litter size and small 6-wk body weight (L+W-); the complementary index (L-W+) and random (K). Females from the five lines and 20 reciprocal F1 crosses were mated to sires of a randomly selected control line (CC). Correlated responses in average direct genetic and average maternal genetic effects for dam body weight and litter size at parturition persisted throughout lactation, indicating important pleiotropic effects. Major correlated responses occurred for litter weight, feed intake and litter feed efficiency, primarily due to average direct genetic effects. Using general combining ability and net line effects as criteria for choosing among lines, L+ had a distinct advantage if the objective was to increase litter size in a crossing program. If the objective was to maximize litter weaning weight, then W+ would be favored for net line effects, while L+ and W+ would be about equivalent for general combining ability. None of the lines had an advantage for litter feed efficiency. Direct heterosis for dam weight at 12 and 21 d of lactation averaged 2.7 and 1.9%, while for litter size the respective averages were 7.4 and 7.3%. The W+ X L+W- cross exhibited overdominance for litter size. Direct heterosis was moderate for feed intake and litter weight, but was negligible for litter feed efficiency because of the mathematical relationship among the three traits. Maternal heterosis for preweaning progeny growth was suppressed because of heterosis for litter size in the dam. Grand-maternal effects on growth of the young were small and would not be an important consideration in choosing among these lines in a crossbreeding program.     

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.     

Genetic parameters for a heavy female turkey line: impact of simultaneous selection for body weight and total egg number

1. The objective of this study was to investigate the strength of the genetic association between growth and reproduction traits in turkeys selected for body weight, conformation and egg production. 2. Two distinct populations but derived from the same heavy turkey female line and situated in different locations (UK and USA), were used to estimate genetic parameters using multivariate REML for the following traits: body weight at 14 (BW14), 19 (BW19) and 24 (BW24) weeks of age and total egg number (EGG). 3. A Box-Cox transformation was applied to egg production data to reduce the impact of non-normality. 4. The heritability estimates for each trait for the UK and USA populations, respectively, were: BW14 0.37 and 0.48; BW19 0.34 and 0.43; BW24 0.28 and 0.43; EGG 0.22 and 0.34. 5. The genetic correlation between the body weight at all ages and the total egg production was strongly negative, reaching a value of -0.75 for the UK and -0.55 for the USA population. 6. The comparison of our results with published estimates in turkeys suggests that the genetic correlation may get stronger in magnitude following selection for increased body weight. 7. This could arise from fixation during selection of genes favouring larger weights but with minimal effect on egg production, leaving the segregating genetic variation dominated by pleiotropic loci with antagonistic effects on the traits. 8. Thus, in order to avoid continued selection for body weight reducing egg production to a point where natural selection offsets selection gains, alternative selection strategies should be considered.     

Genetic parameter estimation for pre- and post-weaning traits in Brahman cattle in Brazil

Beef cattle producers in Brazil use body weight traits as breeding program selection criteria due to their great economic importance. The objectives of this study were to evaluate different animal models, estimate genetic parameters, and define the most fitting model for Brahman cattle body weight standardized at 120 (BW120), 210 (BW210), 365 (BW365), 450 (BW450), and 550 (BW550) days of age. To estimate genetic parameters, single-, two-, and multi-trait analyses were performed using the animal model. The likelihood ratio test was verified between all models. For BW120 and BW210, additive direct genetic, maternal genetic, maternal permanent environment, and residual effects were considered, while for BW365 and BW450, additive direct genetic, maternal genetic, and residual effects were considered. Finally, for BW550, additive direct genetic and residual effects were considered. Estimates of direct heritability for BW120 were similar in all analyses; however, for the other traits, multi-trait analysis resulted in higher estimates. The maternal heritability and proportion of maternal permanent environmental variance to total variance were minimal in multi-trait analyses. Genetic, environmental, and phenotypic correlations were of high magnitude between all traits. Multi-trait analyses would aid in the parameter estimation for body weight at older ages because they are usually affected by a lower number of animals with phenotypic information due to culling and mortality.     

Analysis of beef cattle longitudinal data applying a nonlinear model

The objective of this work was to evaluate the Nelore beef cattle, growth curve parameters using the Von Bertalanffy function in a nested Bayesian procedure that allowed estimation of the joint posterior distribution of growth curve parameters, their (co)variance components, and the environmental and additive genetic components affecting them. A hierarchical model was applied; each individual had a growth trajectory described by the nonlinear function, and each parameter of this function was considered to be affected by genetic and environmental effects that were described by an animal model. Random samples of the posterior distributions were drawn using Gibbs sampling and Metropolis-Hastings algorithms. The data set consisted of a total of 145,961 BW recorded from 15,386 animals. Even though the curve parameters were estimated for animals with few records, given that the information from related animals and the structure of systematic effects were considered in the curve fitting, all mature BW predicted were suitable. A large additive genetic variance for mature BW was observed. The parameter a of growth curves, which represents asymptotic adult BW, could be used as a selection criterion to control increases in adult BW when selecting for growth rate. The effect of maternal environment on growth was carried through to maturity and should be considered when evaluating adult BW. Other growth curve parameters showed small additive genetic and maternal effects. Mature BW and parameter k, related to the slope of the curve, presented a large, positive genetic correlation. The results indicated that selection for growth rate would increase adult BW without substantially changing the shape of the growth curve. Selection to change the slope of the growth curve without modifying adult BW would be inefficient because their genetic correlation is large. However, adult BW could be considered in a selection index with its corresponding economic weight to improve the overall efficiency of beef cattle production.     

Genetic and physiological aspects of growth, body composition and feed efficiency in mice: a review

A review is presented of the genetic and physiological aspects of growth, body composition and feed efficiency in mice. The genetic parameters considered are: nature and extent of within and between-line genetic variation for body weight and growth rate; direct and correlated responses to selection for body weight, weight gain, feed intake and feed efficiency; direct genetic effects of the offspring (gO); maternal genetic effects (gM); heterosis in the offspring (hO); maternal heterosis (hM), and recombination effects in the offspring (rO). The physiological parameters considered are energy requirements for maintenance and growth. The role of thermoregulatory thermogenesis in relation to the partitioning of metabolizable energy between maintenance and growth requirements of large and small mice is emphasized. The relationship of feed efficiency with other traits is reviewed at length.     

Modifying growth curve parameters by multitrait genomic selection

The use of genomic selection for changing the growth curve shape of animals, acting simultaneously on the 3 parameters of a Gompertz growth curve, was studied using computer simulation. Results showed that genomic selection modified the growth curve. Responses to all selection criteria were accompanied with a correlated response in mature weight due to the high genetic correlations between mature weight and the 2 rate parameters. Responses to selection were affected by the loss of accuracy over generations of genomic selection due to the loss of gametic disequilibrium between SNP and genes determining the parameters. In conclusion, genomic selection can be used for changing growth curve parameters. However, changing the whole curve (birth weight, adult BW, and curve shape) is not easy due to the correlation between all BW along the growth of the animal. Applying genomic selection will require a constant reevaluation of the associations between SNP and genes determining the curve parameters.     

Divergent selection for shape of growth curve in Japanese quail. 4. Carcase composition and thyroid hormones

1. Changes in the relative weights of carcase, abdominal fat, breast and leg muscles, and plasma thyroid hormone concentrations occurring during the first 6 weeks of postnatal growth were analysed in males of HG and LG lines divergently selected for high and low relative body weight (BW) gain between 11 and 28 d of age, respectively, and constant adult BW. 2. The second week of postnatal life was a critical age at which the HG males exhibited a relatively faster growth in comparison to their LG counterparts and permanently exceeded LG males in the percentage by weight of carcase, breast and leg muscle. A higher production of muscle tissues was associated with lower accumulation of abdominal fat before sexual maturity. 3. In general, the plasma T(3) level of HG quail exceeded that of LG quail. Nevertheless, significant differences were found only at 14, 21 and 28 d of age, that is, in the period during which the highest inter-line differences in relative growth rate were noted. Also the T(3)/T(4) ratio followed a similar trend while plasma T(4) level showed no clear and consistent inter-line differences. 4. The results suggest that the selection for the shape of the growth curve, like the selection for body fat, modifies the carcase quality owing to shortening/prolongation of the acceleration growth phase. Individuals with a short acceleration phase of the growth curve are characterised by low carcase quality during the fattening period.     

Divergent selection for shape of growth curve in Japanese quail. 3. Onset of sexual maturity and basic characteristics of early lay

1. The onset of lay, quality of eggs during early lay and gonadal development of both sexes were analysed in meat-type lines of Japanese quail, HG and LG divergently selected for high and low relative weight gain between 11 and 28 d of age, respectively, and constant body weight (BW) at 49 d of age. 2. The LG line was sexually mature at an earlier age and lower BW than the HG line. This corresponded with the trend during embryonic and early postnatal development. 3. Analysis of gonads also confirmed earlier sexual development in the LG than in the HG line. In both lines, the growth of testes was detected about one week earlier than the growth of ovary. 4. Despite the different age and BW at onset of lay, HG and LG quail commenced lay at the same degree of maturity (about 90% of adult BW). This implied that the onset of sexual maturity could be identified as a point on the growth curve which terminates the linear phase. 5. When compared with the LG line, the HG line was characterised by a longer acceleration and shorter retardation phase of the growth curve. This difference is seen as an important determinant of line differences in growth and reproductive performance.     

Crossbreeding effects for post-weaning growth traits in a project of Spanish V-line with Baladi Red Rabbits in Egypt

A four-year crossing scheme involving Spanish V line (V) and Egyptian Baladi Red (B) rabbits was carried out to produce five genetic groups: V, B, 1/2B1/2V(F₁), (1/2B1/2V)²(F₂), and ((1/2B1/2V)²)². The last genetic group was considered a new line, named APRI. Body weights (BW) and daily gains in weight (DG) from four to twelve weeks were evaluated for 13,383 rabbits produced by 330 sires and 1074 dams. An animal model was used to estimate heritabilities and common litter effects and a generalized least squares procedure was used to estimate direct additive effects, and direct and maternal heterosis.Heritabilities for growth traits were mostly moderate, ranging from 0.075 to 0.240 for BW and from 0.020 to 0.104 for DG. The V line was heavier and had better gains at each weighing than B rabbits. The F₂ and APRI were also lower in most post-weaning growth performance measures than V line rabbits. APRI rabbits were significantly lighter by 39, 26, 46, 64, and 50 g at ages of 4, 6, 8, 10, and 12 weeks, respectively, relative to the purebred V line, while APRI was significantly heavier by 36 and 127 g relative to the B line at 4 and 12 weeks. The V line, in general, had a higher DG than B line. The differences were 3.15, 7.91 and 1.95 g/d at age intervals of 8–10, 10–12 and 4–12 weeks. Differences in direct additive effects between the two lines were in favor of V line rabbits reaching 15.0% (76 g) at 4 weeks and 13.3% (195 g) at 12 weeks. Direct additive effects for DG were significant during most age intervals reaching 35.7% (7.19 g/d) in the interval of 10–12 weeks. All estimates of direct heterosis were positive and ranged from 4.9 to 16.7% for BW and 14.4 to 29.5% for DG, but the estimates for maternal heterosis were, in most cases, significantly negative and ranging from − 4.5 to − 15.2% for BW and from 20.6 to − 36.9% for DG. If the results are confirmed at commercial farms, the APRI line could be reared in heat stress conditions.     

Reproductive performance in a diallel cross among lines of mice selected for litter size and body weight

Genetic factors affecting female reproductive performance in lines of mice with a known history of selection were estimated from a 5 X 5 diallel cross. Lines were selected as follows: large litter size at birth (L+); large 6-wk body weight (W+); an index for large litter size and small 6-wk body weight (L+W-); the complementary index (L-W+) and randomly (K). Partitioning of direct and correlated responses for litter size, 6-wk body weight and related traits into average direct genetic (li) and average maternal genetic (mi) effects indicated that the magnitude of differences in li exceeded those in mi. Lines having positive responses in li were W+ greater than L+ greater than L-W+ for dam body weight, L+ greater than L+W- greater than W+ for litter size and L+ greater than (W+, L+W-) for litter birth weight, whereas L-W+ responded negatively for litter size. A positive association was found between mi for litter size and dam body weight, W+ and L-W+ being high and L+ and L+W- low for both traits. Female infertility and time from male exposure to parturition had relatively small correlated responses. Line rankings in general combining ability (gi) and net line effects were similar for the respective traits. Depending upon the line and trait involved, the relative contribution of average direct genetic and line direct heterotic (hi) effects to general combining ability [gi = (1/2) li + hi] varied. Line heterosis refers to average heterosis in crosses involving that line. Direct heterosis ( hij ) for each trait differed considerably among crosses. The three crosses showing the highest hij for litter size at birth, W+ X L-W+ (1.78), L+ X W+ (1.28) and L-W+ X L+W- (1.22), possibly had loci contributing directional dominance to litter size with frequencies of parental lines deviating in opposite directions relative to mean gene frequency. The correlation between absolute difference in parental line means and hij for litter size was not significant, suggesting that the magnitudes of absolute differences in parental means were not reliable predictors of divergence in gene frequency. Crossbred performance increased linearly with midparent values for litter size at birth (b = .88 +/- .09, R2 = .92) and dam parturition body weight (b = 1.13 +/- .04, R2 = .99), the latter trait showing an increase (P less than .01) in heterosis as midparent values increased.     

Direct genetic, maternal genetic, and heterozygosity effects on weaning weight in a Colombian multibreed beef cattle population

The (co)variance components of BW at weaning (WW) were estimated for a Colombian multibreed beef cattle population. A single-trait animal model was used. The model included the fixed effect of contemporary group (sex, season, and year), and covariates including age of calf at weaning, age of cow, individual and maternal heterozygosity proportions, and breed percentage. Direct genetic, maternal genetic, permanent environmental, and residual effects were included as random effects. Direct, maternal, and total heritabilities were 0.23 +/- 0.047, 0.15 +/- 0.041, and 0.19, respectively. The genetic correlation between direct and maternal effects was -0.42 +/- 0.131, indicating that there may be antagonism among genes for growth and genes for maternal ability, which in turn suggests that improving WW by direct and maternal EPD may be difficult. A greater value for the direct heterosis effect compared with the maternal heterosis effect was found. Furthermore, the greater the proportion of Angus, Romosinuano, and Blanco Orejinegro breeds, the less the WW.     

黄羽肉鸡群体遗传变异的微卫星分析及其与体重杂种优势的关系

选用10对微卫星引物分析了黄羽肉鸡A、B、C3个品系的遗传结构和差异,并对微卫星标记所计算的个体间遗传距离与C×B、C×A杂交后代的初生至8周龄体重的杂种优势和杂种优势率进行了相关分析。结果表明,10个微卫星标记中有9个表现出多态性,多态信息含量(PIC)和群体杂合度(Heterozigosity)分别为0·4400和0·6811,各品系、各微卫星基因座上都表现出一定差异。利用9个多态微卫星标记计算得出的亲本个体间的遗传距离与后代杂种优势率间多数没有显著的相关(P>0·05),仅C×B组合中亲本个体间平均遗传距离与第8周龄体重杂种优势和杂种优势率间相关显著(P<0·05)。     

Correlated responses of pre- and postweaning growth and backfat thickness to six generations of selection for ovulation rate or prenatal survival in French Large White pigs

Correlated effects of selection for components of litter size on growth and backfat thickness were estimated using data from 3 pig lines derived from the same base population of Large White. Two lines were selected for 6 generations on either high ovulation rate at puberty (OR) or high prenatal survival corrected for ovulation rate in the first 2 parities (PS). The third line was an unselected control (C). Genetic parameters for individual piglet BW at birth (IWB); at 3 wk of age (IW3W); and at weaning (IWW); ADG from birth to weaning (ADGBW), from weaning to 10 wk of age (ADGPW), and from 25 to 90 kg of BW (ADGT); and age (AGET) and average backfat thickness (ABT) at 90 kg of BW were estimated using REML methodology applied to a multivariate animal model. In addition to fixed effects, the model included the common environment of birth litter, as well as direct and maternal additive genetic effects as random effects. Genetic trends were estimated by computing differences between OR or PS and C lines at each generation using both least squares (LS) and mixed model (MM) methodology. Average genetic trends for direct and maternal effects were computed by regressing line differences on generation number. Estimates of direct and maternal heritabilities were, respectively, 0.10, 0.12, 0.20, 0.24, and 0.41, and 0.17, 0.33, 0.32, 0.41, and 0.21 (SE = 0.03 to 0.04) for IWB, IW3W, IWW, ADGBW, and ADGPW. Genetic correlations between direct and maternal effects were moderately negative for IWB (-0.21 +/- 0.18), but larger for the 4 other traits (-0.59 to -0.74). Maternal effects were nonsignificant and were removed from the final analyses of ADGT, AGET, and ABT. Direct heritability estimates were 0.34, 0.46, and 0.21 (SE = 0.03 to 0.05) for ADGT, AGET, and ABT, respectively. Direct and maternal genetic correlations of OR with performance traits were nonsignificant, with the exception of maternal correlations with IWB (-0.28 +/- 0.13) and ADGPW (0.23 +/- 0.11) and direct correlation with AGET (-0.23 +/- 0.09). Prenatal survival also had low direct but moderate to strong maternal genetic correlations (-0.34 to -0.65) with performance traits. The only significant genetic trends were a negative maternal trend for IBW in the OR line and favorable direct trends for postweaning growth (ADGT and AGET) in both lines. Selection for components of litter size has limited effects on growth and backfat thickness, although it slightly reduces birth weight and improves postweaning growth.     

Transgenerational epigenetic variance for body weight in meat quails

We aimed to estimate transgenerational epigenetic variance for body weight using genealogical and phenotypic information in meat quails. Animals were individually weighted from 1 week after hatching, with weight records at 7, 14, 21, 28, 35 and 42 days of age (BW7, BW14, BW21, BW28, BW35 and BW42, respectively). Single‐trait genetic analyses were performed using mixed models with random epigenetic effects. Variance components were estimated by the restricted maximum likelihood method. A grid search for values of autorecursive parameter (λ) ranging from 0 to 0.5 was used in the variance component estimation. This parameter is directly related to the reset coefficient (ν) and the epigenetic coefficient of transmissibility (1‐ν). The epigenetic effect was only significant for BW7. Direct heritability estimates for body weight ranged in magnitude (from 0.15 to 0.26), with the highest estimate for BW7. Epigenetic heritability was 0.10 for BW7, and close to zero for the other body weights. The inclusion of the epigenetic effect in the model helped to explain the residual and non‐Mendelian variability of initial body weight in meat quails.     

Estimation of additive, maternal and non-additive genetic effects of preweaning growth traits in a multibreed beef cattle project

Data from purebred and crossbred calves, consisting of Afrikaner (AF), Charolais (CH), Simmental (ST) and Hereford and Aberdeen Angus combined (HA), were analyzed to estimate breed additive effects, breed maternal effects, average individual heterosis and average maternal heterosis. The traits studied were birthweight (BW), weaning weight (WW) and preweaning average daily gain (ADG) (kg). A multiple regression procedure was used for the estimation of these genetic effects and for predictions for breed crosses that were not included in the data set. Crosses containing higher proportions of CH or ST were heavier at birth and weaning than the other crosses and purebreds. The direct effects of BW were negative and significant (P < 0.05), except that of the CH, which was the highest. The regression coefficients were ?24.87, ?18.16, ?22.80 and ?27.02 for AF, CH, ST and HA, respectively. The maternal effects were not significant. Both average individual and average maternal heterosis regression coefficients were also not significant for BW. Regression coefficients of both direct and maternal effects for WW were not significant and were characterized by large standard errors. Average individual heterosis and average maternal heterosis regression coefficients were, however, significant (P < 0.01) and the values were 5.34 and 2.19, respectively. A similar pattern was observed for ADG, except for the regression coefficients of the maternal effects, which were significant, with larger estimates for AF and ST reflecting their superior mothering ability. The values were 0.01, 0.13, 0.13, 0.03; ?0.82, ?0.85, ?0.85, ?0.81; 0.03 and 0.01 for direct effects and maternal effects of AF, CH, ST and HA; and average individual heterosis and average maternal heterosis, respectively. Means and standard errors of purebreds and their F₁ crosses not included in the dataset were predicted.     

Divergent selection for shape of growth curve in Japanese quail. 1. Responses in growth parameters and food conversion.

1. HG and LG quail lines selected for high and low relative weight gain between 11 and 28 d of age (RG11-28), respectively, and an unselected C line were compared. Mature body weight of both selected lines was held at that of the C line. Progeny of generation 6 were used for analysis. 2. Divergent selection for RG11-28 brought about opposite changes in the growth rates shortly after hatching. 3. Parameters of the Richards function were used to describe the growth curve. The largest differences between HG and LG lines occurred in age (t+) and body weight (y+) at the inflection point of the growth curve (on average for both sexes 28% and 20%, respectively). For HG quail, the parameter t+ was 5 d later than that for LG quail (18.6 vs 14.1 d for males and 20.6 vs 15.6 d for females, respectively), and consequently the parameter y+ was greater (90.3 vs 84.0 g for males and 104.5 vs 96.1 g for females, respectively). The shape of the growth curve expressed by the y+/A ratio was substantialy different for HG and LG quail (44.8% vs 39.6% for males and 43.5% vs 36.8% for females, respectively). 4. The food/gain ratios for the fattening period (3 to 35 d of age) were 3.21, 3.47 and 3.34 for the HG, LG and C lines, respectively. The HG quail started to utilise food more efficiently than the LG quail as early as 10 to 14 d, that is, at the age when their relative growth rate first became greater. 5. The relative deviations of the HG and LG lines from the C line are discussed.     

Weaning weight inheritance in environments classified by maternal body weight change

In good environments, cow intake is sufficient for their own growth and for milk production to support their calf. In poor environments, cows lose BW or may reduce milk supply to maintain themselves. Heritability for direct genetic and maternal components of weaning weight as well as the correlations between these components might be expected to vary according to these circumstances. The purpose of this study was to estimate heritability and genetic correlations for the direct genetic and maternal components of weaning weight classified in 2 environments according to maternal BW gain and to identify whether a single heritability estimate is appropriate for the differing environments experienced by cows from year to year. Data used in this analysis was obtained from the Red Angus Association of America and consisted of 96,064 cow BW observations and 27,534 calf weaning weight observations. A dam's change in BW from one year to the next was used to classify each calf's weaning weight into 1 of 2 environmental groups, those being good or poor. Best linear unbiased estimates of the change in cow BW with age were obtained from analysis of cow BW using a repeatability model. If the phenotypic change in cow BW exceeded this average BW change, the calf's weaning weight associated with the end of this time frame was classified as having been observed in a good environment. If not, the calf's corresponding weaning weight was classified as having occurred in a poorer than average environment. Heritability estimates of 0.24 +/- 0.03, 0.24 +/- 0.03, 0.13 +/- 0.02, and 0.14 +/- 0.02 were obtained for weaning weight good direct, poor direct, good maternal, and poor maternal, respectively. Correlations between direct genetic and maternal weaning weight components in the good and poor environments were -0.47 +/- 0.08 and -0.20 +/- 0.09, respectively. These variance components are not sufficiently distinct to warrant accounting for dam nutritional environment in national cattle evaluation.