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Despite the acknowledged significance of nutrition in bone development, effects of methionine (Met) and cysteine (Cys) on bone quality remain under-researched, particularly during Eimeria challenge. We investigated the effects of different supplemental Met to Cys ratios (MCR) on bone quality of broilers under Eimeria challenge. A total of 720 fourteen-day old Cobb500 broilers were allocated into a 5 × 2 factorial arrangement. Five diets with Met and Cys supplemented at MCR of 100:0, 75:25, 50:50, 25:75, and 0:100 were fed to the birds with or without Eimeria challenge. Body composition was measured by dual energy x-ray absorptiometry, and the femur bone characteristics were assessed by microtomography. Data were analyzed by two-way ANOVA and orthogonal polynomial contrast. The results reaffirmed the detrimental effects of Eimeria challenge on bone quality. On 9 d post inoculation (DPI), significant interaction effects were found for whole body bone mineral content (BMC), lean tissue weight, and body weight (P < 0.05); in the nonchallenged group (NCG), these parameters linearly decreased as MCR decreased (P < 0.05). In the challenged group (CG), body weight and lean tissue weight were unaffected by MCR, and BMC linearly increased as MCR decreased (P < 0.05). For the cortical bone of femoral metaphysis on 6 DPI, bone mineral density (BMD) linearly increased as MCR decreased (P < 0.05). Bone volume to tissue volume ratio (BV/TV) in the CG linearly increased as MCR decreased (P < 0.05). On 9 DPI, BMC and TV linearly increased as MCR decreased (P < 0.05) in the NCG. BMD and BV/TV changed quadratically as MCR decreased (P < 0.05). For the trabecular bone of femoral metaphysis on 9 DPI, BV/TV, and trabecular number linearly increased as MCR decreased (P < 0.05) in the NCG. For the femoral diaphysis, BV, TV, BMC on 6 DPI, and BMD on 9 DPI linearly increased as MCR decreased (P < 0.05). In conclusion, this study showed that both Eimeria challenge and varying supplemental MCR could influence bone quality of broilers., (Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.)

Two trials were carried out to develop and validate linear regression equations for body composition prediction using Dual-energy X-ray absorptiometry (DEXA). In Trial 1, 300 Cobb500 male chickens raised from 1 to 42 d of age were scanned in DEXA to estimate total weight, fat mass, soft lean tissue (SLT) mass, bone mineral content (BMC), and fat percentage. DEXA estimates were compared to body ash, crude fat, SLT (sum of protein and water) and scale body weight. The dataset was split, with 70% used for prediction equations development and 30% for testing, and the 5k-fold cross-validation analysis was used to optimize the equations. The R 2 , mean absolute error (MAE), and root-mean-squared error (RMSE) were used as precision and accuracy indicators. A negative correlation (ρ = -0.27) was observed for ash content, while no correlation was observed for protein content (P > 0.05). Predictive linear equations were developed to assess broiler weight (R 2 = 0.999, MAE = 25.12, RMSE = 38.99), fat mass (R 2 = 0.981, MAE = 13.87, RMSE = 21.28), ash mass (R 2 = 0.956, MAE = 3.98, RMSE = 5.61), SLT mass (R 2 = 0.997, MAE = 35.73, RMSE = 52.45), water mass (R 2 = 0.997, MAE = 29.56, RMSE = 43.94), protein mass (R 2 = 0.989, MAE = 12.94, RMSE = 19.05), fat content (R 2 = 0.855, MAE = 0.81, RMSE = 1.05), SLT content (R 2 = 0.658, MAE = 1.01, RMSE = 1.28), and water content (R 2 = 0.678, MAE = 0.99, RMSE = 1.27). All equations passed the test. In Trial 2, 395 Cobb500 male chickens were raised from 1 to 42 d of age and used for validation of prediction equations. The equations developed for weight, fat mass, ash mass, SLT mass, water mass, and protein mass were validated. In conclusion, DEXA was found to be an effective approach for measuring the body composition of broilers when using predictive equations validated in this study for estimate calibration., (Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.)

In this study, a Lunar Prodigy dual-energy X-ray absorptiometry (DEXA) scanner was validated as a technique to estimate chicken body composition in a non-invasive way. Former research has emphasized the importance of validation of every scanner and software version. In a first trial, DEXA estimated body composition for broilers was correlated with chemical carcass analysis to develop prediction equations. As such, those equations can be used in later experiments with chickens to correct DEXA estimations to estimate body composition accurately by DEXA. DEXA estimated fat mass, lean tissue mass, bone mineral content (BMC) and total body mass, which is the sum of fat, lean mass and BMC, were compared to chemically analyzed crude fat, lean mass as the sum of protein and water and body ash content and scale body weight, respectively. Those regression equations were then used in a second trial to determine body composition based upon DEXA for breeders at different ages. In this experiment, fat and lean tissue determined by DEXA, were compared to dissection parameters commonly used for assessing carcass quality, namely breast muscle and abdominal fat. The first trial showed that DEXA provides high correlations for body mass (ρ = 1) and the individual tissue masses separately (ρ ranging between 0.98 and 1). These high correlations allow for accurate prediction of those components with the developed regression equations. Proportional fat and lean tissue were correlated with their chemical counterparts, however, to a lower extent than absolute values due to lower variation between the proportional weights. BMC percentage was not significantly correlated with ash percentage. Furthermore, in trial 2 high correlations were observed between dissection parameters and DEXA-corrected estimations. These correlations show that DEXA can assess carcass quality in breeders without sacrificing the birds. In conclusion, DEXA is a reliable technique to estimate breeder and broiler body composition in a non-invasive way, hence allowing for longitudinal studies over longer periods of time while avoiding sacrificing of birds., (© 2019 Poultry Science Association Inc.)

Calcium and vitamin D are critical in attenuating metabolic Ca insufficiency often observed in older hens. We investigated interactive effects of dietary Ca and top-dressed 25-hydroxy vitamin D3 (25OHD3) on egg production, eggshell quality (thickness, EST, and breaking strength, ESBS), serum Ca, kidney, liver, and bones attributes in 74-wk old Lohmann LSL-lite layers. A total of 4 levels of Ca (3.0, 3.5, 4.0, and 4.5%) and 3 levels of 25OHD3 (0, 69, and 138 μg/kg) were tested. All diets had basal level of 3,300 IU of vitamin D3/kg, were allocated to 84 individually housed hens (n = 7), and fed to 81 wk of age. Dual-energy X-ray absorptiometry was used to measure bone mineral content (BMC) and density (BMD) in left ulna, femur, and tibia at week 74 (13 spare birds, baseline) and week 81. Birds fed diets containing 3.0, 3.5, 4.0, and 4.5% Ca consumed 3.4, 4.1, 4.2, and 4.8 Ca g/b/d. Interaction (P < 0.05) between Ca and 25OHD3 was such that 25OHD3 linearly increased egg weight and percentage of eggs graded as jumbo (≥70 g) at 3.0, 3.5, and 4.5% Ca levels. There was no interaction (P > 0.05) between Ca and 25OHD3 on the rest of the parameters. Calcium increased EST and ESBS quadratically (P < 0.05), EST increased with Ca intake up to 4.1 g of Ca/b/d whereas Ca intakes (3.4 and 4.8 g of Ca/b/d) had poor ESBS relative to intermediate Ca intakes. Kidney ash concentration increased linearly (P = 009) with Ca intake. However, BMC and BMD in ulna, tibia, and femur declined (P < 0.05) at week 81 relative to baseline. In conclusion, top dressed 25OHD3 linearly increased egg weight at various Ca intakes with no negative effect on eggshell quality or bone attributes. Feeding 4.1 to 4.2 g of Ca/b/d improved eggshell quality, however, higher intake deteriorated eggshell quality and increased renal ash accumulation with no benefit on skeletal integrity., (© 2018 Poultry Science Association Inc.)

A study was conducted to determine the effect of different feeding programs and energy intakes on the body composition of broiler breeders (BB) from 22 wk of age to 65 wk of age. Cobb 500 BB that had been reared using three growth curves: (1) the control group followed Cobb 500 guidelines (SBW) for target body weights (BW), (2) the second group target BW was 20% heavier (HBW) than the SBW group, and (3) the third group target BW was 20% lighter (LBW) than the SBW group. At 21 wk of age, pullets from each growth curve were assigned to be fed one of six treatments. Diets were formulated and allocated to provide 330, 360, 390, 420, 450, or 480 kcal ME/hen/d and 24 g protein/hen/d, at peak intake. Body composition (lean mass, fat mass, and mineral content) was measured by dual-energy x-ray absorptiometry throughout the production period. Significantly, greater (P < 0.05) amounts of fat mass and lower amounts of lean mass were evident at the beginning of the production period for HBW hens compared with SBW and LBW hens. Higher levels of energy intake also affected body composition. Namely, fat deposition was greatest throughout the production period in hens consuming 480 kcal/d at peak intake (P < 0.05). Critically, fluctuations to lean and fat mass throughout the production period are suggestive of underlying regulatory processes. Specifically, hens appears to maintain consistent lean mass throughout the production period with a coefficient of variation of <12% across all birds. The results of this study provide important BB body composition information from management and nutrition studies that showed the dynamics of body composition change during the production period., (© 2018 Poultry Science Association Inc.)

The effect of caponization on the mechanical properties of Polbar chicken bones was the subject of investigation. The biomechanical strength of bones and the risk of their deformation or fracture were determined on the basis of their geometric, structural, material, and densitometric properties. Eight-week-old cockerels of Polbar breed were surgically castrated and then fattened until the 24th week of life. It was observed that caponization did not influence the weight and length of either of the long bones. It did however significantly reduce their ash content and the Ca and P contents in their femur, and P content in their tibia. Dual energy x-ray absorptiometry densitometry revealed that bone mineral content of the mid-diaphyseal part of both bones were reduced. Similarly, the bone tissue density of bones decreased. Caponization influenced the bone's geometric structure increasing the internal and external diameters of the bones. The bone cross-sectional area was greater in capons, and, consequently, the cross-sectional moment of inertia and the radius of gyration significantly increased. However, the relative wall thickness and cortical index were not altered. The three-point bending tests revealed the negative effect of caponization on the mechanical endurance of bones. Yield strength, Young modulus, and yield stress, characterizing the strength of the bone's material, decreased in capons. That suggests a higher risk of permanent deformation as capon bones become less elastic. Concluding, caponization negatively influenced the quality characteristics of Polbar chicken long bones., (© 2016 Poultry Science Association Inc.)

A number of parameters have been used to assess the impact ofcoccidiosis on chickens in clinical settings as well as in experimental studies. However, a rapid way to determine body composition would be useful to evaluate or compare responses to coccidia and could give further insight into the metabolic impact of infection. The current study evaluates the use of dual X-ray absorptiometry (DEXA) to determine the impact of coccidiosis on body composition in chicks receiving inoculations with single or mixed species of Eimeria. Chicks infected with Eimeria maxima, Eimeria acervulina, or Eimeria tenella had altered parameters of body composition as measured by DEXA at 6 days postinfection (PI). The greatest effects were noted in birds infected with E. acervulina or E. maxima, where lean mass and fat were reduced from control values about 75% and 85%, respectively. In chicks infected with E. tenella, tissue and fat were reduced about 10%. Bone mineral content (BMC) was about 75% of control values in birds infected with E. acervulina or E. maxima, but only E. acervulina altered bone mineral density (BMD). The decreases in BMC and BMD are likely due to malabsorption. In chicks receiving a mixed coccidian infection, all DEXA parameters were significantly decreased at 8 days PI compared with age-matched controls. As with single infections, BMD and BMC were significantly depressed (P < 0.05). Values of all DEXA parameters were near 92% of control values by day 16 PI. Analysis of all birds in the current study indicates DEXA tissue weight slightly underestimated the gravimetrically measured weight by about 3%. The current results demonstrate that DEXA is a potentially important tool for the rapid evaluation of the effect of coccidiosis on broiler chicks and suggest it can be useful for evaluation of vaccines and other disease controls.

Quantitative magnetic resonance (QMR) is a nuclear magnetic resonance-based method for measuring the fat, lean, and water content of the total body of the live animal. The purpose of this study was to evaluate the use of QMR for measuring the body composition of chickens while comparing QMR results to those obtained by dual x-ray absorptiometry (DXA) and chemical analysis (CA). A total of 191 birds were scanned live (nonanesthetized) by QMR, killed, and then scanned by DXA. The birds were Ross 708 broiler chickens and ranged in weight from 786 to 3,130 g. In addition, 48 of the carcasses were chemically analyzed for total body lipid, water, and ash content. Compared with CA, QMR underestimated the percentage of total body fat by 34% whereas DXA overestimated the percentage of fat by 50% (10.35 ± 3.35 by CA vs. 6.73 ± 3.90 by QMR and 15.55 ± 4.01 by DXA; P < 0.05). Both QMR and DXA measurements of percentage total body fat were highly correlated with the CA measurement (R(2) = 0.94 and 0.68, respectively). Both QMR and DXA estimates of total body water were close to the CA measurement (1,166 ± 277 g by CA vs. 1,214 ± 279 g by QMR and 1,217 ± 255 g by DXA; P > 0.05), with R(2) values of 0.90 and 0.91, respectively. Based on regression analysis, when prediction equations were applied to the entire group of birds, the QMR and DXA measurements of total body water and total body lean mass were in good agreement, with no significant difference (1,125 ± 244 g vs. 1,135 ± 246 g and 1,377 ± 311 g vs. 1,403 ± 309 g, respectively; P > 0.05) and highly correlated (R(2) = 0.97 for both). Likewise, the QMR measurement of total body fat agreed closely with that measured by DXA (164 ± 48 g and 167 ± 47 g, respectively) and was highly correlated (R(2) = 0.72). The results of this study demonstrate that with proper calibration, both QMR and DXA can provide accurate measurements of the body composition of chickens. The major advantage of the QMR method is that no anesthesia is required, thus facilitating the ease of measurement and repeated measurements.

To determine changes in bone mineralization during molt, 66-wk-old White Leghorns were assigned to either a fasted molting regimen using feed removal for 10 d, followed by the ad libitum consumption of cracked corn for 7 d and a pullet developer diet for 10 d or a nonfasted molting regimen lasting 27 d that included the ad libitum consumption of a diet containing 71% wheat middlings and 23% corn. Both molting regimens restricted light to 8 h/d, and water was provided ad libitum. At 28 d postmolt, hens from both molting treatments were returned to a regular egg-laying diet and 16 h/d of photoperiod. Control hens consumed a regular egg laying diet and were kept on 16 h/d of light throughout the study. Using dual-energy x-ray absorptiometry, bone mineral density (BMD) and bone mineral content (BMC) of the left tibia were measured in 7 live hens per treatment immediately prior to, during, and following the molt. Results showed that by 28 d postmolt, BW loss was 22 and 18% in the fasted and nonfasted molting regimens, respectively (P < or = 0.0001). Compared with premolt values, tibial BMD at 28 d postmolt decreased 35 and 18% in the fasted and nonfasted molt groups, respectively (treatment x age interaction, P < or = 0.0001). Similarly, tibial BMC values decreased 39 and 27% in the fasted and nonfasted molt groups, respectively (treatment by age interaction, P < or = 0.01). The tibial BMD and BMC of controls at 28 d postmolt were similar to premolt values. Recovery in tibial BMD and BMC of fasted and nonfasted hens occurred by 126 d postmolt with values similar to controls. These results suggest that a nonfasted molting regimen is less deleterious to tibial BMD and BMC than a fasted molting regimen.

Dual energy x-ray absorptiometry (DEXA) was evaluated for use as a noninvasive tool to monitor skeletal integrity in live laying hens. The objectives of the current study were 1) to validate the use of DEXA in evaluating bone integrity in live birds as compared with excised bones under a normal nutritional regimen as well as in hens fed varying levels of dietary Ca and 2) to correlate densitometric scans with other bone strength criteria and egg traits. Densitometric scans were conducted on the tibia and humerus of live hens at 10-wk intervals from 17 to 67 wk of age. After each scan, bones were excised from euthanized hens to measure breaking strength characteristics and bone ash (experiment 1). Similar measurements were collected at 38, 48, and 58 wk of age from hens fed hypercalcemic (5.4%), control (3.6%), and hypocalcemic (1.8%) diets from 32 to 58 wk of age (experiment 2). The bone mineral density (BMD) and bone mineral content (BMC) between live and excised bone scans were highly correlated (r = 0.85 and 0.92, respectively, P < 0.0001, experiment 1). Densitometric scans of live birds were positively correlated with bone breaking force and bone ash (r = 0.68 and 0.73, respectively, P < 0.001) with little to no correlation with shell traits. In experiment 2, the excised tibial scan had lower BMD and BMC than the live bird (P < 0.01), whereas no difference was detected in densitometric scans of the humerus. The live and excised BMD and BMC of the tibia (r = 0.87 and 0.82, respectively, P < 0.001) and humerus (r = 0.94 and 0.93, respectively, P < 0.001) were highly correlated. Due to the high correlations between live and excised bone scans and the significant correlations of live scans to more traditional invasive bone measurement tests such as bone breaking force and bone ash, we concluded that DEXA is a useful noninvasive tool for evaluating skeletal integrity in live birds.

1. The aim of this study was to assess bone characteristics in restricted ovulator (RO) hens. These hens generally are unable to ovulate due to a point mutation in the oocyte VLDL receptor gene whose protein product mediates the uptake of yolk precursors. Because these hens do not have the cyclic calcium (Ca) metabolism associated with egg formation, they could be a useful model for studying bone metabolism. 2. RO hens had greater humerus, femur and tibia ash concentrations than wild-type (WT) and out-of-production (OP) hens. Bone mineral content and density obtained with dual-energy X-ray absorptiometry (DXA) were highly correlated with the results of conventional bone assays. 3. Gross and histological examination of the femurs confirmed the presence of extremely dense medullary bone deposition in the RO hens. However, the composition of non-collagenous protein extracts of medullary bone was similar for the two genotypes. 4. Analysis of medullary bone extracts for glycosaminoglycans (GAG) confirmed the presence of large amounts of keratan sulphate (KS) in the matrix of medullary bone. 5. Plasma Ca, total GAG and KS concentrations of RO hens were markedly higher than WT and OP hens. The changes in plasma calcium and keratan sulphate are probably a reflection of elevated Ca-binding yolk precursor molecules and intensive medullary bone formation in response to increased plasma oestrogen observed by others in RO hens.

The purpose of this study was to validate dual-energy x-ray absorptiometry (DXA) for measuring the body composition of chickens in vivo. Four trials were conducted with broiler chickens using a DXA instrument (Lunar, DPX-L) and small animal total body scan software (version 4.7a). In the first 2 trials, the effects of scan mode (high resolution or detail slow), scanning position (ventral or dorsal), and the use of attenuating materials (AM) (2-mm polyvinyl chloride or 4-mm polystyrene) on the precision and values of the DXA parameters body mass, lean tissue mass, fat tissue mass and percentage, bone mineral content (BMC), and bone mineral density (BMD) were evaluated. The precision was highest for body mass and lean tissue mass, followed by BMC and BMD, and was lowest for fat tissue mass and percentage. The precision of the measurements was not influenced by scan mode, position, or type of AM. In contrast, the values for all DXA parameters except body mass were significantly influenced by the scan mode but not by the position. The high resolution mode gave significantly higher estimates of fat mass and BMC but significantly lower measures of lean tissue mass and BMD compared with the detail slow mode. A significant difference between AM was only observed for the DXA estimates of fat tissue mass and fat percentage. In trial 3, the accuracy of the DXA measurements was tested by comparison with chemical body composition analysis. Linear regression equations between the respective DXA and chemical parameters were established. High correlations (r > 0.9; P < 0.0001) were obtained for all parameters, except for fat percentage (r = 0.593; P < 0.05). The purpose of the validation trial was to compare the predicted body composition based on the DXA measurements with established equations and the chemical body composition. There was extremely good agreement for body mass, lean tissue mass, and fat tissue mass and percentage, but not for ash weight. It is concluded that, after proper methodological standardization and application of specifically determined regression equations, DXA can be used for estimating the body composition of chickens in vivo. However, the regression equations are strictly limited to one particular instrument, software version, and applied methodology.

Dual-energy X-ray absorptiometry has been validated in our laboratory as a noninvasive tool to assess skeletal integrity in live birds. The first objective of the current study was to determine if there were detectable changes in bone mineral density (BMD) and bone mineral content (BMC) while an egg was being formed in the oviduct. Implications from this experiment would define the time of day scans should be conducted for future experiments. Densitometric scans were conducted on the tibia and humerus of live hens undergoing active egg formation when hens were 0, 5, 15, and 20 h postoviposition at 24, 30, and 40 wk of age. No detectable changes in either the BMD or BMC of the tibia and humerus were observed as the egg was being formed in the reproductive tract at any age measured. These results suggest that densitometric scans may be conducted on bones in live birds at any time during the day, irrespective of the stage of egg formation. The second objective was to monitor the change and degree of variation in skeletal integrity of live birds during the first cycle of egg laying. The humerus and tibia of White Leghorns were scanned repeatedly at 10-wk intervals from 15 to 65 wk of age. The BMD of the humerus increased from 15 to 65 wk of age, whereas the BMD and BMC of the tibia increased from 15 to 55 wk of age, resulting in a bone-by-age interaction (P < 0.001). The BMC of the humerus did not change from 15 to 55 wk of age but increased at 65 wk of age. Age-related increases in BMD and BMC may be due to the inability of dual energy X-ray absorptiometry to distinguish medullary from structural bone. The CV for BMD and BMC of egg-type chickens was greater than 10% after 25 wk of age, which suggested that bone densitometry could be used as an indicator tool in genetic selection with a potential for improving skeletal integrity of birds.

Dual-energy X-ray absorptiometry can be used as a noninvasive tool to monitor the skeletal integrity of live birds. A pDexa X-ray bone densitometer was used to determine bone mineral densities (BMD) of the left tibia together with the fibula and the humerus of live, unanesthetized birds. Densitometry effectively detected changes in bone integrity of live birds fed varying levels of dietary calcium. Hens consuming 1.8, 3.6, or 5.4% dietary calcium had BMD of 0.147, 0.157, and 0.176 g/cm2 (SEM = 0.005), respectively (linear effect, P < 0.001). Likewise, bone ash weight, breaking force, stress, modulus of elasticity, and eggshell traits also increased linearly in response to increased calcium in the diet (P < 0.05). Densitometric live scans for BMD were positively correlated (P < 0.001) with bone breaking force (r = 0.65) and bone ash (r = 0.77). We also monitored BMD in live Leghorn and broiler females during their life cycle. The tibial BMD of White Leghorns and broilers increased from 15 to 65 wk of age with the BMD of the broiler tibia increasing at a greater rate than that of the Leghorn tibia (line x age interaction, P < 0.0001). A precipitous drop in BMD occurred during an induced molt of Leghorns subjected to 10 d of feed withdrawal. Our long-term goal is to improve skeletal integrity in egg-type chickens by genetic selection for improved BMD. By crossing a broiler with an egg-laying line, an F2 resource population of birds has been developed to identify quantitative trait loci influencing BMD in chickens.

Densitometry was investigated as a noninvasive tool to monitor skeletal integrity in live White Leghorns as an indicator for osteoporosis, a noninfectious disease resulting in mineral loss from the bone. The objectives of the experiment were 1) to assess the ability of densitometry to detect differences in bone integrity in live White Leghorns fed varying concentrations of dietary calcium and 2) to correlate densitometric scans with other bone test methods and production parameters that are sensitive to calcium concentrations in the diet. Hens were fed hypercalcemic (5.4%), control (3.6%), or hypocalcemic (1.8%) diets from 32 to 58 wk of age. A Norland densitometer was used to assess bone mineral density (BMD) and bone mineral content (BMC) of the left tibia and humerus in restrained, unanesthetized hens at 36, 46, and 56 wk of age (experiment 1) and at 38, 48, and 58 wk of age (experiment 2). Bones were excised from hens at 38, 48, and 58 wk of age for breaking strength measurements. Results from the densitometric scans showed that BMD and BMC of the humerus and tibia of live hens decreased linearly when hens consumed diets with decreasing concentrations of calcium (experiment 2). Similar trends in BMD and BMC were detected in experiment 1 at 36 wk of age using BW as a covariate. The results from the densitometric scans were comparable to those obtained from other bone tests commonly used. For example, bone breaking force, stress, and modulus of elasticity decreased linearly as hens consumed decreasing concentrations of calcium. Bone breaking force was correlated with BMD (r=0.65, P<0.001). We concluded that densitometry accurately measures differences in BMD and BMC in live birds fed varying concentrations of dietary calcium.

Dual-energy x-ray absorptiometry (DXA) was evaluated as a method for measuring the body composition of growing broiler chickens. A total of 130 chickens, ranging in weight from 400 to 3,290 g, were scanned using a DXA instrument (Lunar DPX-L). Single whole-body scans were acquired and analyzed using pediatric total body research software (neonatal mode) or small animal total body research software (detail or high resolution mode). The DXA measurements provided readings of total tissue mass, percentage fat, fat tissue mass, lean tissue mass, and bone mineral content. After scanning, the bodies of the chickens were frozen, then, after removing the feathers, homogenized for chemical determination of fat, water, and protein content. By chemical analysis, the whole body fat content of the chickens ranged from 2.8 to 27.2%, giving rise to DXA R values (ratio of attenuation coefficients) ranging from 1.415 to 1.339. The accuracy of DXA for measuring total body fat was a function of the scanning program and mode and also the size of the bird. The best agreement between DXA and chemical measurements of percentage body fat were obtained when chickens weighing more than 2,000 g were scanned using either the small animal-detail mode or neonatal mode. None of the scan modes proved to be accurate for measuring the fat content of birds weighing less than 2,000 g. The DXA measurement of lean mass of chickens was found to be highly correlated with both total body protein (R2 = 0.90) and total body water (R2 = 0.93), but was of little value for predicting percentage values for either. The ratio of DXA bone mineral content to total body ash was 0.77; however, the correlation (R2) between the two was only 0.46. These results suggest that although the DXA technique is potentially useful for measuring body composition of chickens, considerable refinement is needed prior to routine application.

Tibiae were removed from 300 75-wk-old laying hens for tibia strength analysis using two methods, direct photon absorptiometry and tibia breaking strength. Left tibiae with flesh intact were used for bone density determination with direct photon absorptiometry. Right tibiae were cleaned and dried for determination of tibia weight and tibia breaking strength. Partial correlation coefficients were estimated among bone density, tibia breaking strength, tibia weight, and body weight. A significant correlation was observed between tibia breaking strength and bone density measurements (r = .66, P less than or equal to .0001). Tibia weight and tibia breaking strength were also significantly correlated (r = .62, P less than or equal to .0001), as well as bone weight and bone density (r = .71, P less than or equal to .0001). Tibia weight and BW were also significantly correlated (r = .66, P less than or equal to .0001), necessitating covariance adjustment for BW. Bone densitometry measurements are less variable than tibia breaking strength measurements, and bone densitometry does not require cleaning bones of flesh before measurement.