This study was conducted to model the growth of carcass, viscera, and empty body components and component composition of pigs. Quantitative tissue and chemical composition of 319 swine, representative of barrows and gilts from five commercial genetic populations, was determined at eight stages of growth between 25 and 152 kg. After whole body grinding and carcass dissection, proximate analyses were performed to calculate concentrations of protein, lipid, moisture, and ash of carcass, viscera, empty body, carcass lean, and carcass fat. Linear and nonlinear equations were developed to investigate the growth patterns of each component. Nonlinear growth functions accounted for the greatest amount of variation in empty body protein, lipid, moisture, and ash mass. Differences (P < .05) existed between barrows and gilts for nearly all components investigated. Carcass lean and fat tissues significantly increased in lipid percentage and decreased in moisture percentage as live weight increased. There were significant changes in the ratio and composition of the tissues of barrows and gilts during growth. Nonlinear models fitted the data better than allometric equations for nearly all of the components investigated.
No abstract
Carcass and live measurements of 203 pigs representing seven genetic populations and four target live weights (100, 114, 128, and 152 kg) were used to evaluate alternative measures of carcass composition. Measures of carcass lean (fat tissue-free lean, FFLM; lipid-free soft tissue, LFSTIS; and dissected lean in the four lean cuts, DL), fat (total carcass fat tissue, TOFAT), and lipid mass (soft tissue lipid, STLIP) were evaluated. Overall, LFSTIS was 22.8% greater than FFLM (47.8 vs 38.9 kg) and TOFAT was 30% greater than STLIP (38.5 vs 29.6 kg). The allometric growth coefficients relative to carcass weight were different for the measures: b = 0.776, 0.828, 0.794, 1.37, and 1.49 for FFLM, LFSTIS, DL, TOFAT, and STLIP, respectively. At 90 kg carcass weight, the predicted growth of FFLM, LFSTIS, TOFAT, and STLIP was 0.314, 0.420, 0.553, and 0.446 kg/kg increase in carcass weight. The difference between FFLM and LFSTIS, representing nonlipid components of the carcass fat tissue, was greater for barrows than for gilts (9.2 vs 8.6 kg). Lipid-free soft tissue mass was predicted more accurately from carcass or live animal measurements than FFLM with smaller relative RSD (4.6 vs 6.5% of their mean values). The alternative measures of carcass composition were evaluated as predictors of empty body protein (MTPRO) and lipid (MTLIP) mass. Empty body protein was predicted with similar accuracy (R2 = 0.74 to 0.81) from either DL, FFLM, LFSTIS, or ribbed carcass measurements. Empty body lipid was predicted more accurately from TOFAT (R2 = 0.92) or STLIP (R2 = 0.93) than ribbed carcass measurements (R2 = 0.88). Although the alternative measures of lean mass (LFSTIS vs FFLM) and lipid mass (TOFAT vs STLIP) were highly related to each other (r = 0.93 to 0.98), they had different relative growth rates (allometric coefficients) and thus cannot be predicted as linear functions of the similar alternative variable without significant weight group biases. From the 100- to 152-kg target weight groups, gilts gained 12.9% greater FFLM and 12.1% greater MTPRO but only 4.4% greater LFSTIS than barrows. Fat-free lean mass is more precise as a measure of muscle growth and as a predictor of lysine requirements. Lipid-free soft tissue can be obtained more quickly and predicted more accurately from carcass or live animal measurements.
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