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.
This paper compares the growth patterns of chickens, turkeys, ducks and geese. The growth curves and their parameters were estimated by the Richards function. In this work, weight data of females of current sire lines (62 chickens, 47 ducks and 42 geese) and commercial medium-type hybrids (27 turkeys) were used. Birds were fed ad libitum and weighed at 7 or 14 d intervals up to 18-28 weeks of age. The accuracy of the curve fit was high in all species (R 2 = 0.9840 to 0.9994). The ratios y + /A (weight at the inflection point over mature weight), which determine the shape of the growth curve, were 0.370, 0.358, 0.407 and 0.261 in chickens, turkeys, ducks and geese, respectively. Only the growth pattern of the Galliforms did not significantly differ from the Gompertz type of growth (y + /A = 0.368). The age at the inflection point confirmed the high early growth of geese (t + = 21.1 d) and ducks (t + = 25.5 d). The chickens finished the autoacceleration phase of growth at 47.7 d and turkeys at 74.0 d of age. The phenotypic correlations between the inflection parameters t + and y + were higher in waterfowl than in chickens and turkeys. The inflection parameter t + and y + were positively associated with the maturing index k in ducks and geese, and negatively in chickens and turkeys. The evolutionary aspects of the interspecific differences are discussed. growth curve / turkey / waterfowl / chicken / evolution Résumé-Étude comparative des courbes de croissance de volaille. L'article compare les patrons de croissance du poulet, de la dinde, du canard et de l'oie. Les courbes de croissance et leurs paramètres ont été estimés selon l'équation de Richards. L'analyse a porté sur les poids de femelles de lignées paternelles courantes (62 poulets, 47 canards et 42 oies) et de 27 dindes (hybrides commerciaux de type moyen). Les oiseaux ont été nourris ad libitum et pesés régulièrement jusqu'à l'âge de 18 à 28 sem. La précision de l'ajustement des courbes est élevée pour les !! espèces (R 2 = 0,9840 à 0,9994). Le rapport y + /A (poids au point d'inflexion sur poids adulte) qui définit la forme de la courbe de croissance est de 0,370, 0,358, 0,407 et 0,261 pour le poulet, la dinde, le canard et l'oie respectivement. Seul le patron de croissance des Galliformes ne diffère pas significativement de la fonction de Gompertz (y + /A = 0, 368). L'âge au point d'inflexion confirme la précocité de croissance de l'oie (t + = 21, 1 j) et du canard (t + = 25, 5 j). La période d'auto-accélération de la croissance dure 47,7 j chez le poulet et 74 j chez la dinde. Les corrélations phénotypiques entre les paramètres d'inflexion t + et y + sont plus élevées chez le canard et l'oie que chez le poulet et la dinde. Les liaisons entre les paramètres d'inflexion t + et y + et l'index de maturation k sont positives chez le canard et l'oie et négatives chez le poulet et la dinde. Les aspects évolutifs des différences interspécifiques sont discutés dans l'article.
1. The Richards function was used to describe the growth curves (n = 989) of 9 broiler lines. Chickens were fed ad libitum and body weight was recorded every second week from hatching to 26 weeks of age. 2. The accuracy of curve fit measured by the coefficient of determination (R2) was better for males than for females (0.9986-0.9995 vs 0.9972-0.9988, respectively). 3. The estimation of the asymptotic final weight (A) for different lines enabled the degree of maturity (ut = yt/A) to be determined at any fixed point of the curve. At the age of 7 weeks this had a value of 0.318-0.369 for cockerels and 0.325-0.377 for pullets and represented the slaughter maturity of individual lines. The ratio of inflection/asymptotic weight (y+/A = 0.370-0.388) indicated that in some cases chicken growth can be described approximately by the Gompertz function (y+/A = 0.368). 4. It was found that the age at the inflection point of curves (t+ 48.2-55.7 d for cockerels and t+ = 47.8-52.8 d for pullets) roughly corresponds to the slaughter age of the chickens. 5. The interline differences in the parameters of maturation rate for weight (y+/A, k, t+, u7) are low in comparison with the differences in body weight (A, y+, y7) and absolute growth rate (v, v+). 6. The intragroup phenotypic correlation among growth parameters and the importance of the mathematical models are discussed.
1. Embryonic growth and development were analysed using meat type lines of Japanese quail, HG and LG, divergently selected for shape of the growth curve. A total of 1020 embryos of generations 9, 10 or 13 were used for analysis. 2. Considerable inter-line differences were observed in the rate of embryonic development. When compared to HG, LG embryos appeared to be developmentally accelerated during the first 42 h of incubation (larger blastoderm diameter, more somites and higher frequency of more advanced Hamburger-Hamilton stages) as well as at the end of the prenatal period (more embryos with the yolk sac inside the body cavity, shorter incubation period). This corresponded with the trend in postnatal development. 3. Embryonic growth of both lines exhibited an exponential trend. However, considerable inter-line differences were noted in the rate of embryonic growth. Initial growth retardation compensated subsequently by a higher growth rate of HG vs LG quail, characterised the lines after hatching. The same growth pattern repeated three times during the prenatal period (between d 0 and 3, 3 and 8, and 8 and 16). 4. The repeated occurrence of transient decreases in growth rate of the developmentally delayed HG line could be associated with a delayed onset of genetically determined physiological functions mediating utilisation of nutrient supply. 5. Hence, different shapes of growth curves in two genotypes with similar growth potential reveal inter-line differences in physiological age persisting during the whole ontogenesis.
1. Growth curves of two lines (S,D) and their reciprocal hybrids (in total,. n = 344) were evaluated by the Richards function. Geese were weighed at 7 d intervals to the ninth week, and then at 92, 154, 192 and 217 d of age. Food and water were supplied ad libitum. 2. The accuracy of curve fit measured by the coefficient of determination (R2) for different genetic groups ranged from 0.9840 to 0.9918. The highest percentage deviations between observed and estimated live weights were recorded at hatching (on average 15.1%), while at the others points of curve they were significantly lower (from 0.6 to 6.8%). 3. The geese are characterised by an early maturing rate. The peak of the absolute growth rate (the inflection point of the curve) occurred at 18.7 to 23.5 d of age (t+). The degree of maturity at a slaughter age of 63 d (u63 = y63/A) ranged from 0.69 to 0.76. Fitting the inflection point at the beginning of the linear growth phase significantly affects the maturing rate (k) and the ratio between the inflection (y+) and the asymptotic (A) weights. The values of these correlated parameters were very low (y+/A = 0.233 to 0.294, k = 0.0281 to 0.0373 ln theta/d). 4. The live weights of geese from 28 d of age and the parameters of the Richards function were significantly higher (P < 0.05, P < 0.01) in th sire line (S) than in the dam line (D). A low negative heterosis was observed at all points of the growth curves (-0.01 to -9.7%). The results indicated the effect of sex-linked growth genes. 5. The phenotypic correlations between parameters of the Richards function within genetic groups are discussed.
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