Prediction of carcase and breast weights and yields in broiler chickens using breast volume determined in vivo by real-time ultrasonic measurement

1. The use of in vivo real-time ultrasonic (RTU) to predict breast and carcase weights and yields in 103 male broiler chickens was evaluated. Breast area (mm(2)), thickness (mm) and volume (cm(3)) were measured by RTU in three identified sites. After RTU measurements, the broiler chickens were weighed (live weight, LW, g) and slaughtered Carcase and breast weights (g) and physical measures of breast area (mm(2)), and thickness (mm) corresponding to the three identified sites, and volume (cm(3)) were recorded. 2. The best simple correlation between RTU and carcase measurements was obtained for breast volume. Breast and carcase weights were well predicted by LW. Furthermore, breast volume measured in carcase or by RTU was better in predicting breast weight and breast and carcase yields. 3. Multiple regression equations were fitted using LW (g) and RTU measurement of breast volume to predict breast and carcase weights and yields. The coefficients of determination were 0.52 and 0.65 for breast and carcase yields, respectively, and 0.92 and 0.99 for breast and carcase weights, respectively.     

Model for predicting egg output and metabolisable energy intake of laying pullets.

1. The data compiled by Marsden and Morris (1987) to examine the relationships between environmental temperature and the long-term, adapted responses of laying pullets were divided at random into two subsets of 99 and 113 observations. The first subset was used to estimate regression coefficients for an econometric model, and the second subset to validate the model. 2. Equations to predict inputs (costs) and outputs (returns) were estimated with a three-stage least-squares regression model. Three stage least-squares estimation is a technique which corrects for the simultaneity of variables within the model and correlation across equations of the model. This results in more efficient estimates of the regression coefficients. 3. The final output and output equations were: MEI = 253.86-190.31EM+5.766EM2-0.546EM3 + 0.7034T-0.004388T3 + 695.08BW-120.23BW2 + 397.37ME-13.132ME2-1.06MEXT; R2 = 0.86; EO = 119 + 0.025MEI -0.0000045MEI2-1.462T-0.0791T2-135.3BW + 38.31BW2-1.483T X BW + 0.0288T2 X BW + 0.673 delta BW; R2 = 0.59 where MEI = daily metabolisable energy intake (kJ/bird d), T = environmental temperature (degree C), EO = egg output (g/bird d), BW = body weight, and ME = metabolisable energy concentration (kJ/g). The values for R2 indicate very good fits considering that the data were recorded over a 26-year period in 14 different laboratories. 4. This statistical model can serve as the basis for an econometric model of egg production to determine the environmental temperature that maximises profits from laying pullets of different body weights.     

晋南牛体重估测公式的研究

为准确、方便、快速地度量晋南牛的体重 ,运用二元回归原理 ,采用只测量体长 (cm)、胸围 (cm)来估测体重。共测量、验证了 6 90头成年晋南公母牛 ,通过一、二、三类不同膘情的测量、称重、验证 ,总结出一类膘情体重 (kg) =(1.91×体长 (cm) +3.4 7胸围 (cm) - 517.6 )× 1.1;三类膘情体重 (kg) =(1.91×体长 (cm) +3.4 7×胸围 (cm) - 517.6 )× 0 .9,即 :晋南牛体重估测公式为体重(kg) =2×体长 (cm) +3.5×胸围 (cm) - 537,校正系数一类膘为 1.1,三类膘为 0 .9。     

Genetic parameters of ascites-related traits in broilers: correlations with feed efficiency and carcase traits

(1) Pulmonary hypertension syndrome followed by ascites is a metabolic disorder in broilers that occurs more often in fast-growing birds and at cool temperatures. (2) Knowledge of the genetic relationships among ascites-related traits and performance traits like carcase traits or feed efficiency traits is required to design breeding programmes that aim to improve the degree of resistance to ascites syndrome as well as production traits. The objective of this study was to estimate these genetic correlations. (3) Three different experiments were set up to measure ascites-related traits (4202 birds), feed efficiency traits (2166 birds) and carcase traits (2036 birds). The birds in different experiments originated from the same group of parents, which enabled the estimation of genetic correlations among different traits. (4) The genetic correlation of body weight (BW) measured under normal conditions and in the carcase experiment with the ascites indicator trait of right ventricle to total ventricle ratio (RV:TV) measured under cold conditions was 0.30. The estimated genetic correlation indicated that single-trait selecting for BW leads to an increase in occurrence of the ascites syndrome but that there are realistic opportunities of multi-trait selection of birds for improved BW and resistance to ascites. (5) Weak but positive genetic relationships were found between feed efficiency and ascites-related traits suggesting that more efficient birds tend to be slightly more susceptible to ascites. (6) The relatively low genetic correlation between BW measured in the carcase or in the feed efficiency experiments and BW measured in the ascites experiment (0.49) showed considerable genotype by environment interaction. (7) These results indicate that birds with high genetic potential for growth rate under normal temperature conditions have lower growth rate under cold-stress conditions due to ascites.     

Effects of divergent selection for incidence of tibial dyschondroplasia (TD) on purebred and crossbred performance. 2. Processing yield

1. An experiment was conducted to determine the effect of selection for high (H) or low (L) incidence of tibial dyschondroplasia for 7 generations on processing performance of broilers. 2. Birds were obtained from diallel matings of the H and L lines (HH, HL, LH, and LL) and a randombred control (CC) line. Birds were reared to 7 weeks of age under standard management conditions. All birds were processed at 7 weeks of age. Body weight at 7 weeks, carcase weight, and carcase part weights were recorded on each bird. 3. An interaction between sire line and dam line was caused by lighter body and carcase weight at 7 weeks of age in HH birds than from the birds of the other crosses. 4. Birds by L line dams had heavier drumstick weights. The influences of sire line and dam line on weight of total breast muscle were not significant. Thigh weights and Pectoralis minor weights were lighter in HH line birds than those other matings. 5. Heterosis for body weight and for weights of carcases, drumstick and thigh was negative. Total breast muscle weight and P. major weight did not show significant heterosis. 6. It was concluded that selecting against TD does not reduce processing yield of broilers.     

Body weight,meat quality and blood metabolite responses to carbohydrate administration in the drinking water during pre‐slaughter feed withdrawal in broilers

This study was conducted to determine weights of body (BW), carcass (CW), gastrointestinal tract (GTW), meat quality and some blood metabolite responses to corn starch, saccharose or glucose administration in the drinking water during pre‐slaughter feed withdrawal (FW) in broilers. On day 42 of age, 200 broilers (Ross 308) were allocated randomly to five treatments with four replicates. During a 10‐h FW, control broilers (C) were provided with non‐treated water and the standard finisher diet ad libitum, whereas fasted broilers provided with non‐treated (NFW) or treated water, 3 g glucose (G), saccharose (S) or corn starch (CS)/L. Eight birds (four males and four females) per treatment were slaughtered. Birds receiving non‐treated or treated water had lower BW and higher carcass yield than the full‐fed broilers. The full‐fed broilers had higher absolute and relative GTW than the fasted birds. Broilers consumed more readily treated water compared with non‐treated water. While the a* value of breast meat from CS birds was higher than that from NFW, the b* value of that was higher than S and C birds. The c* values of breast meat from S birds were lower compared with that from the CS treatment. The thigh meat from NFW broilers had higher h* value than that from C and G broilers. The thigh meats of C and CS broilers had higher c* value than that of G birds. The full‐fed broilers had higher plasma triglyceride concentration than NFW, S and G birds. The full‐fed broilers had higher plasma uric acid and uric acid nitrogen concentrations than S birds. These results show that carbohydrate administration in the drinking water cannot be a good alternative for the FW period before slaughter due to the fact that the carbohydrates do not reduce BW losses and do not lead to increases in meat quality.     

Effects of dietary protein and energy concentrations on performance and carcase characteristics of chukar partridge (Alectoris chukar) raised in captivity

1. This study was conducted to determine the effects of starter and grower diets with differing crude protein (CP) and metabolisable energy (ME) concentrations on the body weight (BW), live weight gain (LWG), feed consumption (FC), feed conversion ratio (FCR), and carcase, breast+back, rump, wing, neck and abdominal fat weights of chukar partridge raised in captivity. 2. Chukar partridges were fed on starter diets containing 4 concentrations of CP (160, 200, 240, 280 g/kg) and 4 concentrations of ME (10.9, 11.7, 12.6, 13.4 MJ/kg) from hatch to 8 weeks of age; they were fed on grower diets containing 4 concentrations of CP (150, 175, 200, 225 g/kg) and 4 concentrations of ME (11.9, 12.6, 13.2, 13.8 MJ/kg) from 9 to 16 weeks of age. All diets contained at least 5.5 g/kg methionine, 15 g/kg lysine and 10 g/kg methionine+cystine. Sixteen starter and 16 grower diets were arranged in a 4 x 4 factorial design with 4 levels of CP and 4 levels of ME. Each treatment was replicated three times with each replicate consisting of 5 males and 5 females. 3. Partridges fed on a starter diet containing 160 g CP/kg were significantly lighter at 8 weeks of age than those in groups given diets containing a higher CP. However, at 16 weeks of age, the differences in BW among treatments had disappeared. Throughout, there were no significant effects of ME concentration on BW and LWG. 4. The daily mean FC for the 0 to 8 week and 0 to 16 week periods was not affected by dietary CP concentration. For the 9 to 16 week period, the partridges fed on a grower diet containing 225 g CP/kg consumed more feed than those given a diet containing 175 g CP/kg. 5. The highest FCR for the 0 to 8 week period was in partridges fed on a starter diet containing 160 g CP/kg. For the 9 to 16 week period, the lowest FCR was in partridges fed on a grower diet containing 150 g CP/kg. For the 0 to 16 week period, there was not a significant effect of dietary CP concentration on FCR. The daily mean FC and the FCR for the 0 to 8, 9 to 16 and 0 to 16 week periods decreased when the ME concentration of the starter and grower diets increased. 6. The carcase, rump and breast+back weights of the male partridges increased when the ME content of the diets increased. Weights of all carcase components of the male partridges were significantly greater than those of the carcase components of the females. 7. There were no significant interactions between CP and ME concentrations on BW, LWG, FC, FCR and carcase characteristics. 8. We conclude that the starter diet for chukar partridges raised for meat production should contain at least 200 g CP/kg, 11.7 MJ ME/kg, and the grower diet should contain 150 g CP/kg, 12.6 MJ ME/kg.     

Determination of the fourth and fifth limiting amino acids in broilers fed on diets containing maize, soybean meal and poultry by-product meal from 28 to 42 d of age

1. Valine (Val) is considered the 4th limiting amino acid for broilers fed on diets containing ingredients from vegetable origin. However, Val and Isoleucine (Ile) may be co-limiting for broilers fed on diets containing animal protein meals. An experiment was conducted to examine growth responses and meat yield of broilers provided diets varying in digestible Val (dVal) and digestible Ile (dIle) concentrations from 28 to 42 d of age. 2. Eight experimental diets varying in dVal (dVal to dLys ratios from 0·66 to 0·76) and dIle (dIle to dLys ratios from 0·57 to 0·67) were studied; digestible Lysine (Lys) was formulated to 9·9 g/kg in all diets. 3. Broilers fed on a negative control (NC) diet supplemented with crystalline Val (L-Val) and crystalline Ile (L-Ile), dVal to dLys = 0·76 and dIle to dLys = 0·67, grew faster and had higher breast meat yield than birds fed on NC + L-Ile (dVal to dLys = 0·66 and dIle to dLys = 0·67), NC + L-Val (dVal to dLys = 0·76 and dIle to dLys = 0·57), and NC + reduced L-Val and L-Ile (dVal to dLys = 0·71 and dIle to dLys = 0·62). 4. Feeding broilers on the NC + L-Val and L-Ile (dVal to dLys = 0·76 and dIle to dLys = 0·67) diets gave similar BW gain, carcase weight and yield and total breast meat weight and yield to birds fed on the positive control-fed broilers with no added L-Val and L-Ile (dVal to dLys = 0·76 and dIle to dLys = 0·67). 5. These results indicate that Val and Ile are co-limiting in diets containing poultry by-product meal.     

Use of a modified skin slice with subcutaneous fat and carcase weight without this slice for prediction of meatiness and fatness in young slaughter geese

1. White Italian geese (40 males and 40 females) were reared until 12 weeks of age and fed standard diets ad libitum. After rearing ended, the geese were weighed (males-5216 g, females-4945 g) and killed. Carcases were chilled and skin slices with subcutaneous fat removed. The remaining part of the carcase was dissected into meat, intermuscular fat and bones. 2. The weight of a skin slice with subcutaneous fat, taken from the carcase surface excluding the forewings and wing tips (X2), and the weight of a carcase excluding this slice, the forewings and wing tips (X1) were very good indicators of the content of skin with fat (r > 0.99) and meat (r > 0.98) in a whole carcase. 3. The above traits provided a basis for deriving regression equations to estimate the content of meat (Y) or skin with subcutaneous and intermuscular fat (U) in whole carcases of White Italian geese. The following equations are recommended for practical application: Y = 0.755X1 - 27.8 (Sy = 26.3 g); U = 1.070X2 + 19.5 (Su = 11.4 g).     

Effect of dietary dried oregano leaves on growth performance, carcase characteristics and serum cholesterol of female early maturing turkeys

1. A study was conducted with 120 female early maturing turkeys to test the effect of dietary dried oregano leaves (Origanum vulgare subsp. hirtum) on body weight (BW), feed intake (FI), feed conversion efficiency (FCE), carcase characteristics and serum cholesterol concentration. Dried oregano leaves had a content of 3.6 ml essential oils/100 g, while the carvacrol content was 855 g/kg of the total essential oils. 2. From 1 to 84 d of age, the turkeys were fed on 4 diets varying in oregano content (OR0, no oregano--control; OR45, 1.25 g oregano/kg; OR90, 2.5 g oregano/kg; OR135, 3.75 g oregano/kg). Birds were given feed and water ad libitum. 3. BW was unaffected by oregano throughout the experiment. FI and FCE were similar among all treatments until 42 d of age. From 43 to 84 d of age and for the overall experimental period, FI decreased linearly in treatment OR135 and FCE increased linearly with dietary oregano content. Body and carcase weights, carcase yield, and the relative weights of the heart and liver were not significantly affected by oregano content. The relative weights of the gizzard and small intestine decreased linearly with oregano content. Serum cholesterol content was similar among all treatments. 4. In the present study, dietary oregano (1.25, 2.5 and 3.75 g/kg) improved FCE in female early maturing turkeys between 43 and 84 d, with the lowest oregano inclusion (1.25 g/kg) giving the most cost effective diet. Thus, dried oregano leaves may be used as a natural herbal growth promoter for early maturing turkeys.     

Prediction of physical and chemical body compositions of purebred and crossbred Nellore cattle using the composition of a rib section

The goal of this research was to develop empirical equations to predict chemical and physical compositions of the carcass and the body using the composition of the 9th- to 11th-rib section (rib(9-11)) and other measurements. A database (n = 246) from 6 studies was developed and comprised 37 bulls (BU), 115 steers (STR), and 94 heifers (HF), of which 132 were Nellore (NEL), 76 were NEL × Angus crossbreds (NA), and 38 were NEL × Simmental crossbreds (NS). The right half carcass and the rib(9-11) from the left half carcass were analyzed for ether extract (EE), CP, and water. The remaining components were chemically analyzed to determine the composition of the body. A stepwise procedure was used to determine the variable inclusion in the regression models. The variables included were EE in the rib(9-11) (EER; %), CP in the rib(9-11) (CPR; %), water in the rib(9-11) (WR; %), visceral fat (VF; %; KPH and mesenteric fats), organs plus viscera (OV; %), carcass dressing percentage (CD; %), cold carcass weight (kg), and empty BW (EBW; kg). No sex or breed effects were found on EE and CP compositions of the carcass (C(EE) and C(CP), respectively; %); the equations were as follows: C(EE) = 4.31 + 0.31 × EER + 1.37 × VF [n = 241; R(2) = 0.83; mean square error (MSE) = 4.53] and C(CP) = 17.92 + 0.60 × CPR - 0.17 × CD (n = 238; R(2) = 0.50; MSE = 1.58). Breed affected water content in the carcass (C(W), %); the equations were as follows: C(W) = 48.74 + 0.28 × WR - 0.017 × EBW for NEL; C(W) = 46.69 + 0.32 × WR - 0.017 × EBW for NA; and C(W) = 38.06 + 0.48 × WR - 0.017 × EBW for NS (n = 243; R(2) = 0.67; MSE = 5.17). A sex effect was found on body chemical EE composition (BW(EE)); the equations were as follows: BW(EE) = 2.75 + 0.33 × EER + 1.80 × VF for BU; BW(EE) = 1.84 + 0.33 × EER + 1.91 × VF for STR; and BW(EE) = 4.77 + 0.33 × EER + 1.28 × VF for HF (n = 243; R(2) = 0.89; MSE = 3.88). No sex or breed effects were found on CP composition in the body (BW(CP)); the equation was as follows: BW(CP) = 14.38 + 0.24 × CPR (n = 240; R(2) = 0.59; MSE = 1.06). A sex effect was found for body water content (BW(W)); the equations were as follows: BW(W) = 38.31 + 0.33 × WR - 1.09 × VF + 0.50 × OV for BU; BW(W) = 45.67 + 0.25 × WR - 1.89 × VF + 0.50 × OV for STR; and BW(W) = 31.61 + 0.47 × WR - 1.06 × VF + 0.50 × OV for HF (n = 241; R(2) = 0.81; MSE = 3.84). The physical carcass composition indicated a breed effect on all components and a sex effect for fat in the carcass. We conclude that body and carcass compositions can be estimated with rib(9-11) for purebred and crossbred NEL animals, but specific equations have to be developed for different groups of animals.     

The effects of ruminal escape protein or fat on nutritional status of pregnant winter-grazing beef cows

This study was designed to determine the influence of soybean meal supplementation, with or without additional ruminal escape protein or fat, on the nutritional status of pregnant winter-grazing beef cows. During two winters (Trials 1 and 2), approximately 60 prepartum beef cows grazed native foothills range each year. Cows were allotted randomly to five groups and supplemented (g/d) with either none (control); 570 soybean meal (SOY); 450 soybean meal plus 230 blood meal (SOY + BM); 140 soybean meal, 16 urea plus 450 corn gluten meal (SOY + CGM); or 570 soybean meal plus 210 animal fat (SOY + FAT). These supplements were designed to supply similar quantities of ruminal degraded protein while varying in escape protein quantity and source (SOY + BM and SOY + CGM). Condition scores and body weights were determined at trial initiation (mid-December) and conclusion (early March). Eight blood samples obtained over 4 d during three periods (9, 4 and 1 wk prior to parturition) were analyzed for concentrations of glucose, urea nitrogen (N), total bilirubin, creatinine, albumin, total protein and cholesterol. Cows in the control treatment experienced the greatest BW loss in both trials. In Trial 2, escape protein tended to decrease (P less than .06) BW loss compared to SOY, though loss tended to be greater (P less than .08) with SOY + CGM than with SOY + BM. Escape protein can enhance nutritional status when supplemented with .6 kg/d of soybean meal.     

Intrathoracic pressure measurement in cattle: standardized procedure.

A procedure to standardize the position of an esophageal catheter (eso-cat) tip, used to measure intrathoracic pressure, was tested in ten healthy Dutch Friesians. The cattle were in normal condition with body weights (BW) between 52 and 670 kg and thoracic perimeters (TP) between 80 and 210 cm. The position of the neck and head was standardized. The eso-cat was introduced via the nose into the thoracic portion of the esophagus. The distance between the nares and the eso-cat tip (Lcat), which was positioned between the crossing point with the aorta and the caudal mediastinal lymph nodes, was measured for each animal. The regression equation, calculated between the Lcat and the BW and TP was, respectively: Lcat (cm) = 65 + 0.115 x BW (kg) (r2 = 0.99) and Lcat (cm) = 22 + 0.535 x TP (cm) (r2 = 0.97). The corresponding residual standard deviations were respectively 2.52 and 4.37 cm. The multiple and curvi-linear regression equation did not give a significantly better fit of the data.     

Heritabilities and genetic correlations of body weights and feather length in growing Muscovy selected in Taiwan

1. Heritabilities and genetic correlations in the base population of a closed strain of Muscovy duck, moderately selected for body weight at 10 weeks of age, have been estimated from the data of 9 successive generations for the following traits: male and female body weight at 10 and 18 weeks of age (BW10m, BW18m, BW10f, BW18f) and length of the 8th primary feather at 10 weeks of age (F110m, F110f). 2. Multivariate REML with an animal model was used, pooling data from the 9 generations (3283 and 3289 male and female offspring respectively). The same trait expressed in male and female was considered as 2 different traits. 3. The 8th primary feather was longer in females than in males by 6% to 22% at 10 weeks of age. Body weight was heavier in males than in females by 42% to 58% at 10 weeks of age and by 57% to 75% at 18 weeks of age. 3. The heritability estimates for body weight traits showed moderate values, being a little higher for females than for males at the same age, increasing with age from h2=0.24 at BW10m to h2=0.43 at BW18f. 4. The heritability estimates for feather length showed that a greater response would be obtained in selection for male feather length (h2=0.37) than for female length (h2=0.14). Both have high genetic correlations with body weight so they could be indirectly improved. 5. Heritabilities of the difference in body weights between males and females at 10 weeks (h2=0.07) and 18 weeks of age (h2=0.10) were small, as well as for feather length (h2=0.10). It would probably be difficult to modify sexual dimorphism in body weight through selection. 6. Genetic correlations between BW10m, BW18m and BW10f, BW18f were respectively r(g)=0.77 and r(g)=0.80. They were larger for body weight at the same ages between males and females, r(g)=0.90 (r(g)=0.88 between F110m and F110f). Body weight in males and females at the same age should be better considered as 2 different traits in a selection programme. 7. The cumulated predicted genetic gains expressed per unity of the genetic standard deviation (sigma(g)) over the 8 generations of selection were 1.3 sigma(g) and 1.4 sigma(g) respectively for the BW10m and BW10f. The predicted correlated responses were 1.2 sigma(g) for body weights at 18 weeks of age, 0.9 sigma(g) and 0.7 sigma(g) for F110f and F110m respectively.     

Genetic parameters for ultrasound and carcass measures of yield and quality among replacement and slaughter beef cattle.

Real time ultrasound (RTU) measures of longissimus muscle area and fat depth were taken at 12 and 14 mo of age on composite bulls (n = 404) and heifers (n = 514). Carcass longissimus muscle area and fat depth, hot carcass weight, estimated percentage lean yield, marbling score, Warner-Bratzler shear force, and 7-rib dissectable seam fat and lean percentages were measured on steers (n = 235). Additive genetic variances for longissimus muscle area were 76 and 77% larger in bulls at 12 and 14 mo than the corresponding estimates for heifers. Heritability estimates for longissimus muscle area were 0.61 and 0.52 in bulls and 0.49 and 0.47 in heifers at 12 and 14 mo, respectively. The genetic correlations of longissimus muscle area of bulls vs heifers were 0.61 and 0.84 at 12 and 14 mo, respectively. Genetic correlations of longissimus muscle area measured in steer carcasses were 0.71 and 0.67 with the longissimus muscle areas in bulls and heifers at 12 mo and 0.73 and 0.79 at 14 mo. Heritability estimates for fat depth were 0.50 and 0.35 in bulls and 0.44 and 0.49 in heifers at 12 and 14 mo, respectively. The genetic correlation of fat depth in bulls vs heifers at 12 mo was 0.65 and was 0.49 at 14 mo. Genetic correlations of fat depth measured in bulls at 12 and 14 mo with fat depth measured in steers at slaughter were 0.23 and 0.21, and the corresponding correlations of between heifers and steers were 0.66 and 0.86, respectively. Live weights at 12 and 14 mo were genetically equivalent (r(g) = 0.98). Genetic correlations between live weights of bulls and heifers with hot carcass weight of the steers were also high (r(g) > 0.80). Longissimus muscle area measured using RTU was positively correlated with carcass measures of longissimus muscle area, estimated percentage lean yield, and percentage lean in a 7-rib section from steers. Measures of backfat obtained using RTU were positively correlated with fat depth and dissectable seam fat from the 7-rib section of steer carcasses. Genetic correlations between measures of backfat obtained using RTU and marbling were negative but low. These results indicate that longissimus muscle area and backfat may be under sufficiently different genetic control in bulls vs heifers to warrant being treated as separate traits in genetic evaluation models. Further, traits measured using RTU in potential replacement bulls and heifers at 12 and 14 mo of age may be considered different from the corresponding carcass traits of steers.     

Effect of sweet,bitter and soaked micronised bitter lupins on broiler performance

1. The feeding value for broilers of sweet white lupins (Lupinus albus variety Hanti), bitter lupins (Lupinus angustifolius) and soaked micronised bitter lupins was examined.

2. Four isocaloric and isonitrogenous diets were formulated; one contained no lupins and the other 3 contained 400 g/kg sweet, bitter or soaked micronised bitter lupins. The 3 lupin diets were blended appropriately to produce 16 experimental diets containing 0, 50, 100, 200, 300 and 400 g/kg sweet, bitter and soaked micronised bitter lupins, respectively, and these were fed to Ross broilers for 6 weeks.

3. The feeding of diets containing bitter lupins to broilers at 300 and 400 g/kg and soaked micronised bitter lupins at 400 g/kg resulted in significantly different body weights, food intakes, food conversion ratios, carcase moisture and carcase fat contents from those of birds fed on the control diet. No significant differences were observed with carcase protein or carcase ash contents.

4. There were significant linear adverse responses with bitter and soaked micronised bitter lupins in most of the parameters studied whereas no responses were observed with sweet lupins as the dietary inclusion rate of the lupins increased. The soaked micronised bitter lupins performed better than the bitter lupins showing that the amount of bitter lupins in broiler diets can be increased by this method.     

Estimation of endogenous phosphorus loss in growing and finishing pigs fed semi-purified diets

Thirty-six barrows were used in a series of 3 P-balance experiments in which growing and finishing pigs were fed highly digestible, semi-purified diets at or below the dietary available P requirement to estimate the effect of BW on endogenous P loss. Experiments 1, 2, and 3 were conducted with pigs averaging 27, 59, and 98 kg of BW, respectively. In each experiment, pigs were placed in metabolism crates and allotted by weight and litter to 3 dietary treatments. The basal diet consisted of sucrose, dextrose, cornstarch, and casein fortified with minerals (except P) and vitamins. Diets 1, 2, and 3 in Exp. 1 were the basal diet with 0, 0.078, or 0.157% added P, respectively, from monosodium phosphate. In Exp. 2 and 3, diets 1, 2, and 3 were the basal diet with 0, 0.067, and 0.134% added P, respectively, from monosodium phosphate. Within replicate, pigs were fed equal amounts of feed twice daily. Pigs were adjusted to treatments for 7 d before a 6-d, marker-to-marker collection of feces and urine. Phosphorus intakes for pigs fed the 3 diets ranged from 1.73 to 3.91 g/d in Exp. 1, from 2.18 to 5.32 g/d in Exp. 2, and from 1.96 to 6.26 g/d in Exp. 3. Fecal P excretion and P absorption increased linearly (P < 0.05) with increasing P intake. In the 3 experiments, urinary P excretion (g/d) was low for pigs fed diet 1 (0.010, 0.011, 0.019) and diet 2 (0.013, 0.058, 0.084) and was low for pigs fed diet 3 in Exp. 1 (0.037); however, urinary P was greater in pigs fed diet 3 in Exp. 2 and 3 (0.550 and 0.486, respectively). When P absorption (Y, g/d) was regressed on P intake (X, g/d) in Exp. 1, 2, and 3, the relationships were linear (P < 0.01): Y = -0.110 + 0.971X (R2 = 0.999), Y = -0.156 + 0.939X (R2 = 0.998), and Y = -0.226 + 0.8919X (R2 = 0.982), respectively. Thus, our estimates of endogenous P loss at zero P intake were 110, 156, and 226 mg/d for 27-, 59-, and 98-kg pigs, respectively. When these Y-intercepts were regressed on BW, the relationship was Y = 63.06 + 1.632X (R2 = 0.996), where Y = endogenous P loss in mg/d and X = BW in kg. Based on these data, we estimate the endogenous P loss of pigs fed highly digestible, semi-purified diets to increase by approximately 1.632 mg for each 1-kg increase in BW from 25 to 100 kg.     

Dietary isoleucine responses in male broiler chickens

1. Three experiments were conducted to measure growth and carcase responses of growing and finishing broilers fed on test diets formulated to be deficient in isoleucine (Ile). 2. Dose titration methodology was used to measure growth and carcase responses of growing and finishing broilers to graduations of Ile in three additional experiments. 3. The experiments were conducted from d 18 to 30, 30 to 42, and 42 to 56. 4. Broilers given Ile-deficient test diets had poorer weight gain, feed conversion and carcase responses than broilers fed on Ile test diets containing a surfeit of Ile. Adding supplemental Ile to the test diet resulted in equivalent growth and carcase responses to those of broilers fed on the control diet with equal Ile from intact protein sources. 5. Recommended total Ile needs varied between 6.7 and 7.1 g/kg from d 18 to 30, 6.4 to 6.6 g/kg from d 30 to 42, and 5.5 to 6.6 g/kg from d 42 to 56.     

饲用金霉素对肉仔鸡免疫系统生长发育及免疫反应的研究

试验用１日龄ＡＡ商品代肉用公雏５４０只,随机分成３组,每组１８０只,分成１２个重复（１５只／重复）,其中６个重复用作生产性能测定,另６个重复用于测定免疫学指标。在日粮中分别添加０（Ａ组）、５０（Ｂ组）、１５０ｍｇ／ｋｇ（Ｃ组）的金霉素（Ｃｈｌｏｒｔｅｔｒａｃｙｃｌｉｎｅ,ＣＴＣ）。试验表明：（１）在肉久日粮中添加１５０ｍｇ／ｋｇ ＣＴＣ,可以显著地提高肉伍鸡的增重速率和饲料转化效率（Ｐ〈０．０１）     

Effects of oxidised dietary oil and antioxidant supplementation on broiler growth and meat stability

1. Broilers were fed on diets containing oxidised sunflower oil, sunflower oil and sunflower oil supplemented with alpha-tocopherol, butylated hydroxyanisole (BHA) or butylated hydroxytoluene (BHT). 2. Oxidised oil caused a significant reduction in broiler body and carcase weights, whereas alpha-tocopherol and BHA/BHT supplementation improved growth. 3. Meat samples from these broilers were stored at 4 degrees C and -20 degrees C and their oxidative stability evaluated. Feeding oxidised oil to broilers resulted in meat that underwent rapid oxidative changes during refrigerated and frozen storage. 4. On the other hand, dietary alpha-tocopherol and BHA/BHT supplementation increased alpha-tocopherol and BHA/BHT concentrations in meat and significantly (P less than 0.05) improved the oxidative stability of meat during refrigerated and frozen storage.