Effect of frame size, muscle score, and external fatness on live and carcass value of beef cattle.

Commercial slaughter steers (n = 329) and heifers (n = 335) were selected to vary in slaughter frame size and muscle thickness score, as well as adjusted 12th rib fat thickness. After USDA carcass grade data collection, one side of each carcass was fabricated into boneless primals/subprimals and minor tissue components. Cuts were trimmed to 2.54, 1.27, and .64 cm of external fat, except for the bottom sirloin butt, tritip, and tenderloin, which were trimmed of all fat. Four-variable regression equations were used to predict the percentage (chilled carcass weight basis) yield of boneless subprimals at different fat trim levels (.64, 1.27, and 2.54 cm) as influenced by sex class, frame size, muscle score, and adjusted 12th rib fat thickness. Carcass component values, total carcass value, carcass value per 45.36 kg of carcass weight, and live value per 45.36 kg of live weight were calculated for each phenotypic group and external fat trim level. Carcass fatness and muscle score had the most influence on live and carcass value (per 45.36 kg weight basis). Carcasses with .75 and 1.50 cm of fat at the 12th rib were more valuable as the trim level changed from 2.54 cm to .64 cm; however, for carcasses with 2.25 cm of fat at the 12th rib, value was highest at the 2.54 cm trim level. Value was maximized when leaner cattle were closely trimmed. There was no economic incentive for trimming light-muscled or excessively fat carcasses to .64 cm of external fat.     

Deposition and distribution of carcass fat for steers differing in frame size and muscle thickness

Yearling feeder steers (n = 324) representing nine frame size (Large, Medium, Small) x muscle thickness (No. 1, No. 2, No. 3) subclasses were serially slaughtered at 28-d intervals during a 140-d finishing period. Weights for total dissectible (TDF) and subcutaneous fat (SQ) from each of nine wholesale cuts were recorded. Resulting data were analyzed using allometry (Y = aXb and Y = aXb10cx) to characterize deposition patterns for fat and to determine effects of feeder cattle frame size (F) and muscle thickness (M) on relative fat deposition and distribution. Patterns of TDF and SQ deposition were similar among cuts. As the steers became fatter, relative proportions of TDF and SQ in the abdominal and dorsal regions of the carcass increased and relative proportions of fat in the distal regions decreased. There was a tendency for the growth impetus of TDF and SQ to shift from the ventral portions of the carcass toward the dorsal region of the carcass as fattening progressed. Despite significant among-class differences in allometric coefficients, relative proportions of TDF and SQ in the nine wholesale cuts were remarkably similar for all nine F x M subclasses when compared at a constant percentage of total carcass fat. At endpoints of either a constant fat thickness measurement or a constant USDA marbling score, subclass differences in fat distribution were negligible.     

Influence of frame size and body condition score on performance of Brahman cattle

The effects of frame size (FS) and body condition score (BCS) on performance of Brahman cows were evaluated using records collected from 1984 to 1994 at the Subtropical Agricultural Research Station, Brooksville, Florida. Age at puberty (AP), calving rate (CR), calving date (CD), survival rate (SR), weaning rate (WR), birth weight (BWT), weaning weight (WWT), preweaning ADG, and kilograms of calf produced per cow exposed (PPC) were obtained from first- (n = 215), second- (n = 130), and third or greater-parity (n = 267) dams. Based on hip height at 18 mo of age, heifers were assigned to three FS groups: small (115 to 126 cm), medium (127 to 133 cm), or large (134 to 145 cm). Small and medium FS heifers attained puberty at younger (P<.05) ages (633.2+/-12.3 and 626.4+/-12.0 d) than large FS heifers (672.3+/-17.1 d). Calving rate in large FS second-parity dams was 27% less (P<.05) than in small and medium FS dams. In third or greater-parity dams, CR was greater (P<.05) for small FS cows than for medium and large FS cows. Across the three parity groups, CR improved with increasing BCS. Except for the first-parity dams, animals with better fall BCS calved earlier (P<.05). In first-parity dams, SR was less (P<.01) in large (47.9+/-11.0%) than in small (80.7 +/-5.2%) and medium (83.4+/-4.7%) FS groups. Weaning rates of large FS first- and second-parity dams were less (P<.05) than those of small and medium FS dams. Second-parity dams with BCS 3 had lower (P<.05) WR than dams with BCS 4 and 5. Within first- and third or greater-parity dams, BWT of calves born to small FS cows were the lightest, and those born to large FS dams were the heaviest; those born to medium FS dams were intermediate (P<.05). In second-parity dams, BWT of calves of large FS dams were greater (P<.05) than those of small and medium FS dams. In first-parity dams, calves weaned by small FS cows had lower (P<.05) WWT than those weaned by higher FS cows. In the third or greater-parity group, large FS dams weaned heavier calves (P<.05) than other dams. In all parity groups of dams, calves out of large FS cows had greater ADG (P<.05) than those from small and medium FS cows. In first-parity dams, PPC was comparable between small and medium FS dams, but both tended to be greater (P<.10) than PPC of large FS dams. Small and medium FS females reached puberty at an earlier age, calved earlier, and had greater calving, survival, and weaning rates, as well as greater kilograms of calf produced per cow exposed than the large FS females. As the large FS cows matured, they seemed to have overcome the negative effects imposed by FS that were observed at younger ages. Their performance traits were generally all comparable to those of smaller cows once they had reached maturity.     

Effects of degree of fatness in broilers on other carcass characteristics: Relationship between fatness and the composition of carcass fat1

1. Three trials were performed to examine the effect of degree of fatness in broilers on the composition of carcass fat. The various degrees of fatness were obtained by varying the energy to protein (E :P) ratios in conventional diets.

2. Increasing the E : P ratio caused increased fat deposition with increases in the proportions of palmitic and oleic acids and a decrease in linoleic acid.

3. Highly significant negative correlations were obtained between the degree of fatness (expressed as percentage of dry matter of the skin) and of unsaturation of abdominal fat (expressed as iodine value).

4. The same negative correlations were obtained for individuals within the same dietary treatment, especially those producing lean birds.     

Dietary energy density and frame size effects on composition of gain in feedlot cattle

Experiments were conducted to evaluate the effects of dietary energy density or genetic background on protein and fat gain of growing cattle. In Exp. 1, 24 Limousin steers were used in a growing-finishing trial. A 2 X 2 factorial arrangement was used with steers randomly allotted to four treatment combinations and fed the following diets: 80% concentrate, high moisture corn-corn silage diet (HI) or a corn silage diet (LO) during both the growing (GRO) and(or) the finishing (FIN) phases. Body composition for both experiments was determined by a deuterium oxide dilution technique. Empty body weight gains were greater (P less than .05) for HI during GRO, FIN and the total trial. Daily protein gains (DPG) were greater (P less than .05) for HI during GRO and FIN, while cattle receiving HI during at least FIN had the greatest (P less than .05) overall DPG. Daily fat gains (DFG) followed the pattern of DPG, being more rapid (P less than .05) for cattle fed HI during either GRO or FIN. Cattle fed the HI diet also tended to be more energetically efficient. In Exp. 2, large frame (LG) and small frame (SM) cattle were used for the evaluation of frame size effects on protein and fat deposition. Steers were individually fed an 80% concentrate, corn-based diet during the entire trial. Average daily gains and daily dry matter intake (P less than .05, P less than .01) were greater for LG, while feed efficiency was similar for both cattle types. Large cattle had greater (P less than .05) DPG than SM cattle, however, DFG were not different. Small frame steers were energetically more efficient (P less than .05), apparently due to composition of gain difference.     

Response time of broiler chickens to cimaterol: meat tenderness, muscle composition fiber size, and carcass characteristics.

The response time to cimaterol (CIM), a beta-adrenergic agonist, by broiler chickens for carcass characteristics, muscle composition, muscle fiber size, catheptic enzyme activity, and tenderness was determined. Two trials were conducted in which chickens were fed a control diet (CON) containing 0 ppm of CIM or a diet containing 1 ppm of CIM. Trial 1 consisted of 55, 31-d-old broiler chickens individually fed for up to 48 h. At 0, 6, 12, 18, 24, and 48 h, five CON and five CIM-fed chickens were killed. Trial 2 consisted of 160, 33-d-old broiler chickens group-fed for up to 14 d. At 2, 4, 6, 8, 10, 12, and 14 d, 10 CON and 10 CIM-fed chickens were killed. The breast muscle (BM) and leg muscle (LM) weight, cathepsin B and L activities, DNA, RNA, and protein concentration, and BM shear force value (SFV) were measured in both trials. Thigh muscle (TM) SFV were measured in Trial 2 only. Fiber size of BM was measured (five birds per treatment) at d 2, 6, 10, and 14. In Trial 1, BM weight and SFV were lower in CIM-fed birds at 6 h (P less than .05). In Trial 2 BM SFV were higher at d 8 (P = .06) and d 10 (P less than .05) in CIM-fed chickens. The SFV of CIM-fed chickens were higher at d 4, 8, 10, 12, and 14 (P less than .05).(ABSTRACT TRUNCATED AT 250 WORDS)     

Genetic variation in fatness and fatty acid composition of crossbred cattle

Mature Hereford cows (766) were mated to 97 sires from seven breeds (Jersey, Wagyu, Angus, Hereford, South Devon, Limousin, and Belgian Blue), resulting in 1,215 calves born over 4 yr (1994 to 1997). These cattle comprised Australia's 'Southern Crossbreeding Project." Heifers were slaughtered at an average of 16 mo with hot standard carcass weight of 219 kg and 9 mm fat over the rump. Steers were slaughtered at an average of 23 mo with carcass weight of 319 kg and 13 mm fat over the rump. Meat and fat samples were taken from the carcass on the day after slaughter for subsequent laboratory analysis of i.m. fat content and fatty acid composition. Data were analyzed using uni- and bivariate animal models containing fixed effects of cohort, management group, birth month, and sire breed. March-born calves had fat with a 0.5 degrees C lower melting point, 0.6% higher total monounsaturated fatty acids, and 0.7% higher fatty acid desaturation index than calves born in April. Steers born in 1997 were the only cohort finished on pasture, and they had much more yellow fat than the other cohorts. Four heavy breed crosses (Angus, South Devon, Limousin, and Belgian Blue) averaged 284 kg carcass weight, followed by purebred Hereford (268 kg), Wagyu (244 kg) and Jersey (236 kg). Angus had the greatest fat depth (14.3 mm), ahead of Hereford and Wagyu (11.9 mm), Jersey (10.7 mm), South Devon and Limousin (9.9 mm) and Belgian Blue (8.0 mm). Jersey, Wagyu, and Angus had themost i.m. fat (4.6%), followed by Hereford and South Devon (3.8%), and Limousin and Belgian Blue (3.1%). The highly marbled Jersey and Wagyu had softer fat (6% lower fat melting point) than the other breeds. Angus were more highly marbled, similar to Jersey and Wagyu, but had harder fat similar to the leaner breeds. Heritabilities for all traits were low to moderate (16 to 36%). Genetic correlations between fatty add composition and carcass traits were not significant, indicating little evidence of antagonisms between traits that would prevent genetic progress in both production and quality.     

Predicting carcass composition of beef cattle using ultrasound technology.

We evaluated 20 slaughtered cattle with ultrasound before hide removal to predict fat thickness and ribeye area at the 12th rib for possible use in carcass composition prediction. Carcasses were fabricated into boneless subprimals that were trimmed progressively from 2.54 to 1.27 to .64 cm maximum fat trim levels. Stepwise regression was used to indicate the relative importance of variables in a model designed to estimate the percentage of boneless subprimals from the carcass at different external fat trim levels. Variables included those obtained on the slaughter floor (ultrasound fat thickness and ribeye area; estimated percentage of kidney, pelvic, and heart [KPH] fat; and warm carcass weight) and those obtained from carcasses following 24 h in the chill cooler (actual fat thickness, actual ribeye area, estimated percentage of KPH fat, warm carcass weight, and marbling score). At all different subprimal trim levels, percentage KPH was the first variable to enter the model. In the models using measures taken on the slaughter floor, ultrasound fat thickness was the only other variable to enter the model. Ultrasound fat thickness increased R2 and decreased residual standard deviation (RSD) in models predicting subprimals at 2.54-cm maximum fat trim; however, at 1.27- and .64-cm trim levels, R2 and RSD increased. Models using the same two variables (except actual fat instead of ultrasound) in the cooler were similar to those using data from the slaughter floor. However, as more cooler measurement variables entered the models, R2 increased and RSD decreased, explaining a greater amount of the variation in the equation. Ultrasonic evaluation on the slaughter floor may be of limited application compared with the greater accuracy found in chilled carcass assessment.     

Genetic evaluation of carcass traits in Simmental-sired cattle at different slaughter end points

Our objectives were to estimate genetic parameters for carcass traits and evaluate the influence of slaughter end point on estimated breeding values (BV). Data provided by the American Simmental Association were divided into three sets: 1) 9,604 records of hot carcass weight (CW) and percentage retail cuts (PRC), 2) 6,429 records of CW, PRC, and marbling score (MS), and 3) 1,780 records of CW, PRC, MS, fat thickness (FT), and longissimus muscle area (LMA). Weaning weights (WW) from animals with carcass data and from their weaning contemporaries were used. Data were analyzed with a multiple-trait animal model and REML procedures to estimate genetic parameters and BV on an age-, CW-, MS-, or FT-constant basis. The model for carcass traits included fixed contemporary group and covariates for breed, heterozygosity, and slaughter end point and random additive direct genetic and residual effects. Weaning weight was preadjusted for founder effects, direct and maternal heterosis, age of dam, and age of calf. The model for WW included fixed contemporary group and random additive direct genetic, maternal genetic, maternal permanent environment, and residual effects. Heritabilities from data set 1 were 0.34 for CW and 0.25 for PRC on an age-constant basis and 0.25 for PRC on a CW end point. Heritabilities for data set 2 were 0.35, 0.24, and 0.36 for CW, PRC, and MS, respectively, on an age-constant basis. Data set 2 heritabilities were 0.25 for PRC and 0.34 for MS on a CW-constant basis and 0.33 for CW and 0.25 for PRC at a constant MS end point. Heritabilities on an age-constant basis for data set 3 were as follows: CW, 0.32; PRC, 0.09; MS, 0.12; FT, 0.10; and LMA, 0.26. Heritability estimates for data set 3 on a CW-, MS-, and FT-constant basis were similar to those on an age-constant basis. Heritabilities were 0.12 for PRC, 0.12 for MS, 0.14 for FT, and 0.22 for LMA on a CW-constant basis; 0.30 for CW, 0.09 for PRC, 0.10 for FT, and 0.28 for LMA at a constant MS end point; and 0.33, 0.17, 0.13, and 0.29 for CW, PRC, MS, LMA on a FT-constant basis. Genetic correlations among traits varied across groups and end points but suggested that it should be possible to select for improved lean yield without sacrificing quality grade. Correlations were calculated among BV computed at different end points. Adjustment to various end points resulted in some changes in BV and reranking of sires, especially for PRC; however, the number of records available had a larger influence than slaughter end point.     

An evaluation of the USDA standards for feeder cattle frame size and muscle thickness

This study was conducted to determine the live weights at which large-, medium-, and small-framed feeder steers and heifers attain a degree of finish associated with a carcass quality grade of low Choice and to examine the relationship of feeder cattle muscle thickness to carcass yield grade traits. Feeder steers (n = 401) and heifers (n = 463) representing three age classes (calf, yearling, long yearling) were selected randomly at a commercial feedlot to exhibit wide ranges in frame size and muscularity. Individual weights were recorded and a panel of five experienced evaluators scored each animal for frame size, muscle thickness, and flesh condition. The cattle were finished on a high-concentrate finishing diet and harvested at an estimated carcass fat thickness of 10 mm. Final weights and USDA carcass grade data were collected for all cattle. Frame size scores effectively predicted finished weight at a marbling end point of Small(00) for both heifers (r2 = 0.89, SE = 16 kg) and steers (r2 = 0.94, SE = 13 kg). For heifers, the Small/Medium and Medium/ Large frame score intersects corresponded to live weights of 460 kg and 520 kg, respectively. For steers, the Small/Medium and Medium/Large frame score lines corresponded to live weights of 504 kg and 577 kg, respectively. These weights were greater than weights specified in the 1979 USDA grade standards. Evaluations of feeder cattle muscling, based on 1979 USDA Standards, were associated (P < 0.05) with differences in longissimus muscle area but were not related (P = 0.08) to differences in numerical carcass yield grades. An alternative muscle thickness classification scheme, involving the use of four thickness classes, was effective for stratifying feeder cattle according to eventual differences (P = 0.004) in carcass yield grade. Our findings suggest that USDA feeder cattle grade standards developed in 1979 are no longer adequate for describing today's population of feeder cattle.     

青贮饲用高粱对肉牛屠宰性能、胴体品质的影响

为探究青贮饲用高粱对肉牛屠宰性能、胴体品质的影响,综合考虑各种青贮饲用高粱的营养搭配是否满足肉牛营养需要,以期推动中国现代肉牛经济发展。研究以西门塔尔三代阉牛为试验牛,以BJ0603青贮饲料作为基础饲粮。饲喂试验结束后,每个日粮处理组挑选3头牛进行屠宰分割,测定屠宰性能及胴体品质。结果表明,不同比例的青贮高粱和青贮玉米不仅会影响肉牛的采食量和日增重,还会间接影响肉牛的产肉性能。随着日粮中青贮饲用高粱比例的增加,肉牛的采食量降低,能量摄入不足,影响机体内脂肪的正常沉积,降低了肉的嫩度。但对牛肉常规营养成分无显著影响,对其肉色影响显著。     

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.     

Leptin as a predictor of carcass composition in beef cattle

Our objective was to determine if serum concentrations of leptin could be used to predict carcass composition and merit in feedlot finished cattle. Two different groups of crossbred Bos taurus steers and heifers were managed under feedlot conditions near Miles City, MT. The first group consisted of 88 1/2 Red Angus, 1/4 Charolais, and 1/4 Tarentaise composite gene combination steers (CGC) harvested at the ConAgra processing facility in Greeley, CO. The second group (Lean Beef Project; LB) consisted of 91 F2 steers and heifers born to Limousin, Hereford, or Piedmontese by CGC F1 cows crossed to F1 bulls of similar breed composition and harvested at a local processing facility in Miles City, MT. Blood samples were collected approximately 24 h before harvest (CGC) or approximately 3 d before and at harvest (LB). No differences in serum concentrations of leptin were detected (P > 0.10) between Hereford, Limousin, or Piedmontese F2 calves nor between LB steers and heifers. Positive correlations (P < 0.01) existed between serum leptin and marbling score (r = 0.35 and 0.50), fat depth measured between the 12th and 13th rib (r = 0.34 and 0.46), kidney, pelvic, and heart fat (KPH) (r = 0.42 and 0.46), and quality grade (r = 0.36 and 0.49) in CGC and LB cattle, respectively. Serum leptin was also positively correlated with calculated yield grade for CGC steers (r = 0. 19; P = 0. 10) and LB cattle (r = 0.52; P < 0.01). Longissimus area was not correlated with serum leptin in CGC steers (r = 0.12; P > 0.10). However, a negative correlation existed between longissimus area and serum leptin in the LB cattle (r = -0.45; P < 0.01). Serum concentrations of leptin were significantly associated with carcass composition (marbling, back fat depth, and KPH fat) and quality grade in both groups of cattle studied and may provide an additional indicator of fat content in feedlot cattle.     

Evaluation of estimated genetic merit for carcass weight in beef cattle: Blood metabolites, carcass measurements, carcass composition and selected non-carcass components

In Ireland, a new beef genetic index has been developed. Growth rate is expressed as expected progeny difference for carcass weight (EPD_CWT) and is estimated on an across-breed basis. Cross-breeding of dairy cows with both Aberdeen Angus and Belgian Blue beef sires is widely practised. The objective of this study was to compare blood metabolites, slaughter traits and carcass composition of progeny from Holstein–Friesian dairy cows and Aberdeen Angus (AA), Belgian Blue (BB), Friesian (FR) and Holstein (HO) sires. The AA and BB sires were selected, within breed, to be of either high (H) or low (L) estimated genetic merit for carcass weight. A total of 170 male progeny from spring-calving cows and 42 sires (10 AA, 13 BB, 7 FR and 12 HO) were artificially reared indoors and managed together until the end of their second grazing season when they were assigned to either a Light (560 kg) or Heavy (620 kg) slaughter weight. Blood metabolite concentrations were measured six times throughout life and feed intake was recorded during the first and second winter. Carcass measurements and selected non-carcass components were recorded after slaughter and the right side of each carcass was dissected into lean, fat and bone. Differences in blood metabolite concentrations amongst genetic groups were negligible although there were some effects of the prevailing level of nutrition. M. longissimus area scaled for carcass weight was 0.220, 0.221, 0.260, 0.255, 0.212 and 0.208 (SE 0.004) cm²/kg for AAH, AAL, BBH, BBL, FR and HO, respectively. Carcass measurements scaled for carcass weight were greater for L, AA, HO and the dairy strains than for H, BB, FR and the beef breeds, respectively. There was no effect of estimated genetic merit for carcass weight on carcass composition. Statistically significant interactions between genetic merit and beef breed existed for some traits with the genetic merit effect largely evident for AA only. BB and the beef breeds had more lean, less fat and more high value lean in the carcass than AA and the dairy strains, respectively. It is concluded that genetic group had little effect on blood metabolite concentrations but there were some feeding level effects. Estimated genetic merit for carcass weight affected carcass weight, m. longissimus area and carcass measurements scaled for carcass weight but the effects were confined to AA. There were large effects of beef breed and dairy strain on carcass composition.     

Effect of diet composition and slaughter weight on animal performance, carcass and meat quality, and fatty acid composition in veal calves

The effect of true milk use in the diet of Spanish Brown Swiss male calves on animal performance, carcass and meat quality, and fatty acids composition was studied. In experiment 1, the effect of milk intake [ad libitum continuous (ADLIB) feed vs. restricted 0.7 during 75 days followed by ad libitum feed (RESTR)] and slaughter endpoint (225 kg vs. 5 month) were studied. In experiment 2, ad libitum concentrate feeding [grain-fed (GF)] was compared with milk supplementation until slaughter [milk-fed (MF)] in calves slaughtered at 345 kg. As regards to milk intake, carcass weight and degree of fatness were higher in the ADLIB group (P<0.05). The RESTR group revealed a higher percentage of saturated fatty acids (P<0.05). In experiment 2, the MF group exhibited a higher fat percentage (P<0.05), lower press and cooking losses (P<0.05), and higher scores for tenderness and juiciness (P<0.05) than the GF group. The percentage of saturated fatty acids was higher in the MF group (P<0.05). The results suggest that true milk use in veal production could be an advantageous alternative in terms on production costs, animal performance, and carcass and meat quality.     

The effect of dietary protein supply on carcass composition, size of organs, muscle properties and meat quality of pigs

This study investigated the effect of dietary protein supply on growth performance, carcass composition and size of organs in pigs slaughtered at the age of 165 ± 2 d. In addition, we analysed muscle fibre properties and glycolytic potential of light muscles longissimus lumborum (LD), semimembranosus (SM), and gluteus superficialis (GS), and dark muscles infraspinatus (IS) and masseter (M) of 20 gilts and 20 barrows. Of these pigs, 16 were Finnish Landrace, 16 were Finnish Yorkshire, and 8 were crosses of these breeds. The pigs were fed low-or high-protein diets formulated to contain 6.0 and 9.5 g of apparent ileal digestible lysine/feed unit (1 fu = 9.3 MJ NE), respectively. The pigs were fed according to a restricted weight-based feeding scale (13–30 MJ NE/d). Lean meat, fat, bones, and skin of the carcasses as well as organs were dissected and weighed. The pH value was measured 45 min post mortem from LD, and 24 h post mortem from LD, SM and GS. Drip loss, lightness (L) and redness (a) were measured from LD, SM and GS. Pigs with a low-protein supply showed a lower growth rate (P < 0.01), carcass weight (P < 0.01), and carcass lean meat content (P < 0.01), but higher carcass fat content (P < 0.01) and smaller kidneys (P < 0.01) than did pigs with a high-protein supply. In LD, the differences in cross-sectional areas in all muscle fibre types (P < 0.05) between the feeding groups were significant; in GS we found significant differences in cross-sectional areas of type IIA and type IIB (P < 0.05), while in SM we found no differences in muscle fibre cross-sectional areas between the feeding groups (P > 0.05). We found no such differences in the dark muscles studied. We also took into account the effect of both the breed and sex on the studied properties. The low-protein diet increased glycolytic potential in porcine LD and SM, and decreased the pH value measured 45 min post mortem from LD. The dietary protein supply affected no other meat quality traits studied. A more rapid drop in pH in LD resulted in a lighter and less red meat with higher drip loss.     

Detection of quantitative trait loci for growth and carcass composition in cattle

The objective of the present study was to detect quantitative trait loci for economically important traits in a family from a Bos indicus x Bos taurus sire. A Brahman x Hereford sire was used to develop a half-sib family (n = 547). The sire was mated to Bos taurus cows. Traits analyzed were birth (kg) and weaning weights (kg); hot carcass weight (kg); marbling score; longissimus area (cm2); USDA yield grade; estimated kidney, pelvic, and heart fat (%); fat thickness (cm); fat yield (%); and retail product yield (%). Meat tenderness was measured as Warner-Bratzler shear force (kg) at 3 and 14 d postmortem. Two hundred and thirty-eight markers were genotyped in 185 offspring. One hundred and thirty markers were used to genotype the remaining 362 offspring. A total of 312 markers were used in the final analysis. Seventy-four markers were common to both groups. Significant QTL (expected number of false-positives < 0.05) were observed for birth weight and longissimus area on chromosome 5, for longissimus area on chromosome 6, for retail product yield on chromosome 9, for birth weight on chromosome 21, and for marbling score on chromosome 23. Evidence suggesting (expected number of false-positives < 1) the presence of QTL was detected for several traits. Putative QTL for birth weight were detected on chromosomes 1, 2, and 3, and for weaning weight on chromosome 29. For hot carcass weight, QTL were detected on chromosomes 10, 18, and 29. Four QTL for yield grade were identified on chromosomes 2, 11, 14, and 19. Three QTL for fat thickness were detected on chromosomes 2, 3, 7, and 14. For marbling score, QTL were identified on chromosomes 3, 10, 14, and 27. Four QTL were identified for retail product yield on chromosomes 12, 18, 19, and 29. A QTL for estimated kidney, pelvic, and heart fat was detected on chromosome 15, and a QTL for meat tenderness measured as Warner-Bratzler shear force at 3 d postmortem was identified on chromosome 20. Two QTL were detected for meat tenderness measured as Warner-Bratzler shear force at 14 d postmortem on chromosomes 20 and 29. These results present a complete scan in all available progeny in this family. Regions underlying QTL need to be assessed in other populations.     

Association of myostatin on early calf mortality, growth, and carcass composition traits in crossbred cattle

The objective of this study was to investigate a potential association of an inactive myostatin allele with early calf mortality, and evaluate its effect on growth and carcass traits in a crossbred population. Animals were obtained by mating F1 cows to F1 (Belgian Blue x British Breed) or Charolais sires. Cows were obtained from mating Hereford, Angus, and MARC III (1/4 Hereford, 1/4 Angus, 1/4 Pinzgauer, and 1/4 Red Poll) dams to Hereford, Angus, Tuli, Boran, Brahman, or Belgian Blue sires. Belgian Blue was the source of the inactive myostatin allele. Myostatin genotypes were determined for all animals including those that died before weaning. Early calf mortality was examined in the F2 subpopulation (n = 154), derived from the F1 sires mated to F1 cows from Belgian Blue sires, to evaluate animals with zero, one, or two copies of inactive myostatin allele. An overall 1:2:1 ratio (homozygous active myostatin allele:heterozygous:homozygous inactive myostatin allele) was observed in the population; however, a comparison between calves dying before weaning and those alive at slaughter showed an unequal distribution across genotypes (P < 0.01). Calves with two copies of the inactive allele were more likely (P < 0.01) to die before weaning. Postweaning growth traits were evaluated in the surviving animals (n = 1,370), including birth, weaning, and live weight at slaughter, and postweaning ADG. Carcass composition traits analyzed were hot carcass weight, fat thickness, LM area, marbling score, USDA yield grade, estimated kidney, pelvic, and heart fat, retail product yield and weight, fat yield and weight, bone yield and weight, and percentage of carcasses classified as Choice. Charolais lack the inactive myostatin allele segregating in Belgian Blue; thus, in the population sired by Charolais (n = 645), only animals with zero or one copy of the inactive myostatin allele were evaluated. Animals carrying one copy were heavier at birth and at weaning, and their carcasses were leaner and more muscled. In the population sired by Belgian Blue x British Breed (n = 725), animals with two copies of inactive myostatin allele were heavier at birth, leaner, and had a higher proportion of muscle mass than animals with zero or one copies. Heterozygous animals were heaviest at weaning and had the highest live weight, whereas animals with zero copies had the highest fat content. The use of the inactive myostatin allele is an option to increase retail product yield, but considerations of conditions at calving are important to prevent mortality.