Slaughter Group Research Articles

Meat production traits of local Karayaka sheep in Turkey 1. The meat quality characteristic of lambs

This study is an investigation into the meat quality parameters of Karayaka lambs at different slaughter weights (SWs). The single-born Karayaka male lambs (n=30) selected for this study were an average live-weight of 20 kg and weaned at 2.5-3 months of age. The animals with pre-specified SWs were divided into slaughter weight (SW) groups (30, 35, 40, 45 and 50 kg) using a fully randomized design. To determine the M. longissimus dorsi et thoracis (LD) muscle meat quality characteristics, six lambs from each weight group were slaughtered. Results revealed significant differences among the slaughter groups with regard to pH, color parameters (L*-lightness, a*-redness, b* -yellowness), cooking loss (CL), drip loss (DL), moisture (M), crude protein (CP) and intramuscular fat (IF) ratios. Increasing water holding capacities (WHCs) and hardness values were observed with increasing SW. Significant differences were also observed among the slaughter groups with regard to total monounsaturated fatty acid + total polyunsaturated fatty acid/total saturated fatty acid ratios and total cholesterol content.

Energy and protein requirements of non-descript breed hair lambs of different sex classes in the semiarid region of Brazil.

The aim of this study was to determine the energy and protein requirements of non-descript breed hair lambs (NDB) reared under Brazilian semiarid conditions. Sixty animals from three sex classes (20 intact males, 20 castrated males, and 20 females) with an average initial body weight of 18.1 ± 0.4 kg and an average age of 5 months were used. The nutritional requirements were estimated using the comparative slaughter. The animals in the final slaughter group were distributed in a completely randomized design with a 3 × 3 factorial scheme (three sex classes and three feeding levels: ad libitum feeding (positive energy balance), 70% feed restriction (maintenance level), and 80% feed restriction (negative energy balance)). The net energy requirement for maintenance (NEm) did not differ between sex classes (P > 0.05) and it was 68 kcal/kg of metabolic empty body weight (EBW(0.75))/day (P < 0.05). The coefficients for the nonlinear regression of retained energy (RE) on the empty body weight gain (EBWG) were not different among the different sex classes (P > 0.05). The net energy requirement for weight gain (NEg) was estimated by NEg (Mcal/day) = 0.29 × EBW(0.75) × EBWG(0.86) for all sex classes (P < 0.05). The net protein requirement for weight gain (NPg) was estimated by NPg (g/day) = 224.45 × EBWG - 0.025 × RE for all sex classes (P < 0.05). The NEg increased and the NPg decreased with the increase in body weight of NDB lambs.

Energy requirements for growth of pubertal female Saanen goats.

Previous research on energy requirements of female Saanen goats, using the factorial approach, has not considered the specific requirements for maintenance and growth during the pubertal phase. Thus, the purpose of this study was to estimate energy requirements for maintenance (Trial 1) and growth (Trial 2) of non-pregnant and non-lactating female Saanen goats at the pubertal phase from 30 to 45kg. In Trial 1, the net energy requirements for maintenance (NEm ) were estimated using 18 female Saanen goats randomly assigned to three levels of intake: adlibitum, and 70% and 40% of adlibitum intake. These animals were pair-fed in six slaughter groups, each consisting of one animal for each level of intake. In Trial 2, the net energy requirements for growth (NEg ) were estimated using 18 female Saanen goats, which were fed adlibitum and slaughtered at targeted BW of 30, 38 and 45kg. The NEm was 52kcal/kg(0.75) of BW. The NEg increased from 3.5 to 4.7Mcal/kg of BW gain as BW increased from 30 to 45kg. Our results suggest that the guidelines of the major feeding systems for the entire growth phase may not be adequate for females at pubertal phase.

Macromineral requirements of Dorper×thin-tailed Han crossbred female lambs

A comparative slaughter trial was conducted to determine the net mineral requirements for maintenance and growth of Dorper crossbred female lambs raised from 20 to 35 kg of body weight (BW). Thirty-five Dorper×thin-tailed Han crossbred female lambs of (20.3±1.14) kg BW were used: 7 lambs were randomly chosen and slaughtered at the beginning of the experiment as the baseline group for measuring the initial body composition; another 7 lambs were randomly chosen and offered a pelleted mixed diet ad libitum and slaughtered at (27.0±0.73) kg BW; the remaining 21 lambs were randomly divided into 3 groups of 7 animals each and subjected to the same diet either ad libitum or at 70 or 40% of ad libitum intake. The 21 lambs were fed in 7 slaughter groups, with each group consisting of one lamb from each treatment (ad libitum, 70 or 40% of ad libitum intake). The 3 groups were slaughtered when the sheep fed ad libitum attained (33.8±0.52) kg of BW. The body composition of five minerals (Ca, P, Na, K, and Mg) was determined. The net mineral requirements for maintenance were 35.01, 25.18, 9.30, 31.35, and 2.03 mg kg−1 empty BW (EBW) for Ca, P, Na, K, and Mg, respectively, and the net growth requirement per kg of EBW gain ranged from 9.73 to 8.87 g of Ca, 5.83 to 5.27 g of P, 1.73 to 1.63 g of Na, 3.73 to 4.08 g of K, and 0.26 to 0.25 g of Mg for Dorper crossbred lambs in China, respectively. The estimates of mineral requirements with Dorper crossbred lambs in the current study were not consistent with the recommendations from previous studies.

Effect of Different Slaughter Weights on Slaughter and Carcass Traits of Male Karayaka Lambs Reared under Intensive Production System

The present study was conducted to investigate the carcass traits of Karayaka lambs slaughtered at different slaughter weights (SWs) and to find out optimum SWs. Male Karayaka lambs with 20 kg live weight (n=30) constituted the animal material of the study. Lambs were randomly divided into five SW groups; 30 (GI; n=6), 35 (GII; n=6), 40 (GIII; n=6); 45 (GIV; n=6) and 50 (GV; n=6) kg. Lamb fattening feed (concentrate feed, ad libitum) and forage (lentil straw, 100g/lamb/day) were used as the feed material. Lambs were sent to slaughter at target SWs. Following the slaughter, non-carcass components, tailless hot and cold carcass weights were taken. Carcasses were separated into six sections as leg, foreleg, back, loin, neck and others. Physical dissection was performed to investigate carcass composition. Only the differences in carcass dressing and skin percentages of slaughter groups were not found to be significant. Increasing carcass fat percentages and decreasing carcass lean and bone percentages were observed with increasing SWs. Considering the consumer preferences, current findings revealed that Karayaka lambs should be sent to slaughter at weights between 30-35 kg. However, considering the red meat deficit of the country, current market conditions and producer preferences, the optimum SW for Karayaka lambs were recommended to be between 40-45 kg.

Effect of Age on Energy Requirement for Maintenance and Growth of Dorper and Hu Crossbred F1 Ewes Weighing 20 to 50 kg.

This research aimed to define the energy requirement of Dorper and Hu Hybrid F1 ewes 20 to 50 kg of body weight, furthermore to study energy requirement changes with age and evaluate the effect of age on energy requirement parameters. In comparative slaughter trial, thirty animals were divided into three dry matter intake treatments (ad libitum, n = 18; low restricted, n = 6; high restricted, n = 6), and were all slaughtered as baseline, intermediate, and final slaughter groups, to calculate body chemical components and energy retained. In digestibility trial, twelve ewes were housed in individual metabolic cages and randomly assigned to three feeding treatments in accordance with the design of a comparative slaughter trial, to evaluate dietary energetic values at different feed intake levels. The combined data indicated that, with increasing age, the net energy requirement for maintenance (NEm) decreased from 260.62±13.21 to 250.61±11.79 kJ/kg0.75 of shrunk body weight (SBW)/d, and metabolizable energy requirement for maintenance (MEm) decreased from 401.99±20.31 to 371.23±17.47 kJ/kg0.75 of SBW/d. Partial efficiency of ME utilization for maintenance (km, 0.65 vs 0.68) and growth (kg, 0.42 vs 0.41) did not differ (p>0.05) due to age; At the similar condition of average daily gain, net energy requirements for growth (NEg) and metabolizable energy requirements for growth (MEg) for ewes during late fattening period were 23% and 25% greater than corresponding values of ewes during early fattening period. In conclusion, the effect of age upon energy requirement parameters in the present study were similar in tendency with previous recommendations, values of energy requirement for growth (NEg and MEg) for Dorper and Hu crossbred female lambs ranged between the NRC (2007) recommendation for early and later maturating growing sheep.

Influence of electrical stimulation on carcass and meat quality of Kosher and conventionally slaughtered cattle

In a previous study regarding the effects of Kosher and conventional slaughter techniques on carcass and meat quality of cattle, it was speculated that electrical stimulation may have affected some of the meat qualities. Therefore, the objective of this study was to investigate the effects of electrical stimulation (ES) and non-electrical stimulation (NES) on key carcass and meat quality attributes of cattle slaughtered by Kosher vs. conventional slaughter methods. Carcass pH and temperature profiles over a 24 h post mortem (pm) period, meat shear force and water holding capacity were investigated in feedlot type cattle of comparable weights and breed types. Results showed that the combined effects of slaughter methods did not influence the meat quality attributes, but there were differences within the slaughter groups. The effect of ES on carcass pH lasted longer within the conventionally slaughtered group (12 h), than in the Kosher slaughter group (6 h). Muscle samples from the ES groups for both slaughter methods were more tender. Electrical stimulation also had a significant effect on the cooking loss from Kosher meat, while there was no significant difference in meat from the conventional slaughter methods. The results show that ES influences certain meat and carcass quality attributes of cattle, based on the way cattle were slaughtered.Keywords: Carcass pH, cooking loss, drip loss, electrical stimulation, shear force, slaughter technique

Effects of in utero heat stress on postnatal body composition in pigs: I. Growing phase.

Environmentally induced heat stress (HS) negatively influences production variables in agriculturally important species. However, the extent to which HS experienced in utero affects nutrient partitioning during the rapid lean tissue accretion phase of postnatal growth is unknown. Study objectives were to compare future whole-body tissue accretion rates in pigs exposed to differing in utero and postnatal thermal environments when lean tissue deposition is likely maximized. Pregnant sows were exposed to thermoneutral (TN; cyclical 15°C nighttime and 22°C daytime; n = 9) or HS (cyclical 27°C nighttime and 37°C daytime; n = 12) conditions during their entire gestation. Twenty-four offspring from in utero TN (IUTN; n = 6 gilts and 6 barrows; 30.8 ± 0.2 kg BW) and in utero HS (IUHS; n = 6 gilts and 6 barrows; 30.3 ± 0.2 kg BW) were euthanized as an initial slaughter group (ISG). Following the ISG, 48 pigs from IUTN (n = 12 gilts and 12 barrows; 34.1 ± 0.5 kg BW) and IUHS (n = 12 gilts and 12 barrows; 33.3 ± 0.3 kg BW) were exposed to constant HS (34.1 ± 2.4°C) or TN (21.5 ± 2.0°C) conditions until they reached 61.5 ± 0.8 kg BW, at which point they were sacrificed and their whole-body composition was determined. Homogenized carcasses were analyzed for N, crude fat, ash, water, and GE content. Data were analyzed using PROC MIXED in SAS 9.3. Rectal temperature and respiration rate increased (P < 0.01) during postnatal HS compared to TN (39.4 vs. 39.0°C and 94 vs. 49 breaths per minute, respectively). Regardless of in utero environment, postnatal HS reduced (P < 0.01) feed intake (2.06 vs. 2.37 kg/d) and ADG (0.86 vs. 0.98 kg/d) compared to TN conditions. Postnatal HS did not alter water, protein, and ash accretion rates but reduced lipid accretion rates (198 vs. 232 g/d; P < 0.04) compared to TN-reared pigs. In utero environment had no effect on future tissue deposition rates; however, IUHS pigs from the ISG had reduced liver weight (P < 0.04; 17.9%) compared to IUTN controls. In summary, postnatal HS reduced adipose tissue accretion rates, but IUHS did not appear to impact either lean or adipose tissue accretion during this specific growth phase.

Effects of in utero heat stress on postnatal body composition in pigs: II. Finishing phase.

The detrimental effects of heat stress (HS) on animal productivity have been well documented. However, whether in utero HS interacts with a future thermal insult to alter tissue deposition during the finishing phase of pig growth is unknown. Study objectives were to compare the subsequent rate and quantity of whole-body tissue accretion in pigs exposed to differing in utero and postnatal thermal environments. Pregnant sows were exposed to thermoneutral (TN; cyclical 15°C nighttime and 22°C daytime; n = 9) or HS (cyclical 27°C nighttime and 37°C daytime; n = 11) conditions during their entire gestation. Twenty-four offspring from in utero TN (IUTN; n = 6 gilts and 6 barrows; 62.4 ± 0.7 kg BW) and in utero HS (IUHS; n = 6 gilts and 6 barrows; 61.9 ± 0.8 kg BW) were euthanized as part of an initial slaughter group (ISG). After the ISG, 48 pigs from IUTN (n = 12 gilts and 12 barrows; 66.1 ± 1.0 kg BW) and IUHS (n = 12 gilts and 12 barrows; 63.4 ± 0.7 kg BW) were exposed to constant HS (34.4 ± 1.8°C) or TN (22.7 ± 2.5°C) conditions until they reached 80.5 ± 1.5 kg BW, at which point they were sacrificed and their whole-body composition was determined. Homogenized carcasses were analyzed for N, crude fat, ash, water, and GE content. Data were analyzed using PROC MIXED in SAS 9.3. Rectal temperature and respiration rate increased during postnatal HS compared to TN (39.6 vs. 39.3°C and 92 vs. 58 breaths per minute, respectively; P < 0.01). Postnatal HS decreased (P < 0.01) feed intake (2.13 vs. 2.65 kg/d) and ADG (0.70 vs. 0.94 kg/d) compared to TN conditions, but neither variable was influenced by in utero environment. Whole-body protein and lipid accretion rates were reduced in HS pigs compared to TN controls (126 vs. 164 g/d and 218 vs. 294 g/d, respectively; P < 0.04). Independent of postnatal environments, IUHS reduced future protein accretion rates (16%; P < 0.01) and tended to increase lipid accretion rates (292 vs. 220 g/d; P < 0.07) compared to IUTN controls. The ratio of lipid to protein accretion rates increased (95%; P < 0.01) in IUHS pigs compared to IUTN controls. In summary, the future hierarchy of tissue accretion is altered by IUHS, and this modified nutrient partitioning favors adipose deposition at the expense of skeletal muscle during this specific phase of growth.

Models for predicting energy requirements in meat quail

Three experiments were conducted to determine the metabolizable energy (ME) required for the maintenance (MEm) and growth (MEg) of quail and to develop models for predicting the ME requirements for growing quail. The Exp. 1 was conducted to determine the actual ME of food for quails fed at different levels (ad libitum and 70%, 50%, and 30% of ad libitum intake). Eighty quails in metabolism cages (35-d-old) were assigned to treatments in a completely randomized design (CRD) with 5 replicates of 4 quails each. The average N-corrected apparent ME (AMEn) values obtained were 12.33, 12.15, 12.11, and 13.22MJ/kg for quails fed ad libitum and 70%, 50%, and 30% of ad libitum intake. The Exp. 2 was conducted to obtain the requirements of MEm, net energy (NE) for maintenance (NEm), and efficiency (k) of energy utilization using the comparative slaughter technique and regression. Six hundred-twenty (15-d-old) were assigned to 4 treatments with 5 replicates of 31 quails each in a CRD. The diet used in Exp. 1 was also offered in Exp. 2. The values obtained for the MEm and NEm, were 659 and 310kJ/kg0.75/d, respectively. The values for the efficiency of fat (kf) and crude protein (kp) deposition and overall efficiency of energy utilization (kfp) and maintenance efficiency (km) were 0.79, 0.32, 0.47, and 0.47, respectively. The Exp. 3 was conducted to determine the MEg requirement. Five hundred (1-d-old) were assigned to 10 slaughter groups (replicates) with 5 groups of 55 quails in each of 2 periods, 0–14 and 14–35d of age. Quails were slaughtered weekly and the chemical body composition of the quail was determined. The MEg values for the periods 0–14 and 14–35d of age were 12.2 and 18.8kJ/g, respectively, which was determined by dividing the NE required for weight gain by the efficiency of dietary ME utilization. The equations for predicting energy demands were determined considering the ME intake (MEI), the metabolic weight of the quails (W0.75), and the weight gain per quail/d (G), and prediction equations were MEI=659W0.75+12.2G and MEI=659W0.75+18.8G.

Energy requirements in early life are similar for male and female goat kids.

Little is known about the gender differences in energetic requirements of goats in early life. In this study, we determined the energy requirements for maintenance and gain in intact male, castrated male and female Saanen goat kids using the comparative slaughter technique and provide new data on their body composition and energy efficiency. To determine the energy requirements for maintenance, we studied 21 intact males, 15 castrated males and 18 females (5.0±0.1 kg initial body weight (BW) and 23±5 d of age) using a split-plot design with the following main factors: three genders (intact males, castrated males, and females) and three dry matter intake levels (ad libitum, 75% and 50% of ad libitum intake). A slaughter group included three kids, one for each nutritional plane, of each gender, and all three animals within a group were slaughtered when the ad libitum kid reached 15 kg in BW. Net energy requirements for gain were obtained for 17 intact males, eight castrated males and 15 females (5.1±0.4 kg BW and 23±13 d of age). Animals were fed ad libitum and slaughtered when they reached 5, 10, and 15 kg in BW. A digestion trial was performed with nine kids of each gender to determine digestible energy, metabolizable energy and energy metabolizability of the diet. Our results show no effect of gender on the energy requirements for maintenance and gain, and overall net energy for maintenance was 205.6 kJ/kg0.75 empty body weight gain (EBW) (170.3 kJ/kg0.75 BW) from 5 to 15 kg BW. Metabolizable energy for maintenance was calculated by iteration, assuming heat production equal to metabolizable energy intake at maintenance, and the result was 294.34 kJ/kg0.75 EBW and km of 0.70. As BW increased from 5 to 15 kg for all genders, the net energy required for gain increased from 9.5 to 12.0 kJ/g EBW gain (EWG), and assuming kg = 0.47, metabolizable energy for gain ranged from 20.2 to 25.5 kJ/g EWG. Our results indicate that it is not necessary to formulate diets with different energetic content for intact male, castrated male and female Saanen goat kids weighing from 5 to 15 kg.

Energy requirements for maintenance and growth of male saanen goat kids.

The aim of study was to determine the energy requirements for maintenance and growth of forty-one Saanen, intact male kids with initial body weight (BW) of 5.12±0.19 kg. The baseline (BL) group consisted of eight kids averaging 5.46±0.18 kg BW. An intermediate group consisted of six kids, fed for ad libitum intake, that were slaughtered when they reached an average BW of 12.9±0.29 kg. The remaining kids (n = 27) were randomly allocated into nine slaughter groups (blocks) of three animals distributed among three amounts of dry matter intake (DMI; ad libitum and restricted to 70% or 40% of ad libitum intake). Animals in a group were slaughtered when the ad libitum-treatment kid in the group reached 20 kg BW. In a digestibility trial, 21 kids (same animals of the comparative slaughter) were housed in metabolic cages and used in a completely randomized design to evaluate the energetic value of the diet at different feed intake levels. The net energy for maintenance (NEm) was 417 kJ/kg0.75 of empty BW (EBW)/d, while the metabolizable energy for maintenance (MEm) was 657 kJ/kg0.75 of EBW/d. The efficiency of ME use for NE maintenance (km) was 0.64. Body fat content varied from 59.91 to 92.02 g/kg of EBW while body energy content varied from 6.37 to 7.76 MJ/kg of EBW, respectively, for 5 and 20 kg of EBW. The net energy for growth (NEg) ranged from 7.4 to 9.0 MJ/kg of empty weight gain by day at 5 and 20 kg BW, respectively. This study indicated that the energy requirements in goats were lower than previously published requirements for growing dairy goats.

The incidence of dark cutting in southern Australian beef production systems fluctuates between months

Dark cutting is detrimental to meat quality and therefore is the major cause of carcass downgrades under the Meat Standards Australia grading system. This study quantified the variation between months in the incidence of dark cutting, in southern Australia. Four years of Meat Standards Australia grading data, from nine individual beef processors in Western Australia, South Australia, Victoria and Tasmania, was utilised for the analysis. The dataset contained 42 162 slaughter groups, of 10 or more grass-fed cattle, which allowed for the percentage of dark cutters per slaughter group to be analysed. The interaction between month, year and state was significant (P &lt; 0.001). The lowest risk of dark cutting for South Australia and Western Australia was in October (1.53% ± 0.75 and 6.96% ± 0.76) and November in Tasmania and Victoria (7.34% ± 0.9 and 5.27% ± 0.81) potentially when feed availability and quality is highest. The incidence of dark cutting was highest for all states during the period from February to June. Lower pasture availability and quality in combination with higher levels of stress due to extreme high or low temperatures during this time could all contribute to the higher incidences. The findings of this study show that procurement and management decisions made by cattle buyers, producers and processors need to change throughout the year to help mitigate the incidence of dark cutting carcasses and reduce financial loss.

Models to predict muscle tissue and crude protein in beef cattle

Two experiments were conducted to estimate the amount of muscle tissue and crude protein (CP) in carcasses and in empty body (EB) weight from urinary creatinine excretion (UCE). In experiment I 32 Nellore bulls were used with an initial body weight of 259±24.9kg and 14±1 month old, as follow: four bulls were fed at maintenance level and the 28 bulls had ad libitum access to feed throughout the experiment. The diet consisted of corn silage and concentrate (55:45). Three days before each slaughter, total urine was collected from all bulls within a slaughter group. After harvest, a complete dissection (fat, lean and bone) of the left half of the carcass was conducted and subsampled. Sub-samples were lyophilized, partially defatted and ground for further evaluation. In experiment II 15 Nellore heifers were allocated by body weight into three groups: 127±24.2kg (low), 221±22.3kg (medium) and 434±29.2kg (high). Heifers were fed a diet consisting of 60% of corn silage and 40% of concentrate. After 30 days of adaptation, total urine was collected over a three day period using Folley catheters. After urine collection, the animals were slaughtered to estimate the physical composition of the carcasses and EB. The amounts of muscle tissue present in the carcasses of Nellore bulls and heifers (Mcarc) was estimated using the following equation: Mcarc (kg)=14.40×UCE (g/d). The amount of CP in the carcasses (CPcarc) and the empty bodies (CPEB) of Nellore bulls was estimated by: CPcarc=3.85×UCE (g/d) and CPEB=5.86×UCE (g/d), respectively. It was concluded that each gram of UCE corresponded with 14.40kg of muscle tissue, 3.85kg of CP in the carcass and 5.86kg of CPEB.

Effects of dietary soybean oil on pig growth performance, retention of protein, lipids, and energy, and the net energy of corn in diets fed to growing or finishing pigs1

The objectives of this experiment were 1) to determine if dietary soybean oil (SBO) affects the NE of corn when fed to growing or finishing pigs, 2) to determine if possible effects of dietary SBO on the NE of corn differ between growing and finishing pigs, and 3) to determine effects of SBO on pig growth performance and retention of energy, protein, and lipids. Forty-eight growing (initial BW: 27.3 ± 2.5 kg) and 48 finishing (initial BW: 86.0 ± 3.0 kg) barrows were used, and within each stage of growth, pigs were allotted to 1 of 6 groups. Two groups at each stage of growth served as an initial slaughter group. The remaining 4 groups were randomly assigned to 4 dietary treatments and pigs in these groups were harvested at the conclusion of the experiment. A low-lipid basal diet containing corn, soybean meal, and no added SBO and a high-lipid basal diet containing corn, soybean meal, and 8% SBO were formulated at each stage of growth. Two additional diets at each stage of growth were formulated by mixing 25% corn and 75% of the low-lipid basal diet or 25% corn and 75% of the high-lipid basal diet. Results indicated that addition of SBO had no effects on growth performance, carcass composition, or retention of energy, protein, and lipids but increased (P < 0.05) apparent total tract digestibility of acid hydrolyzed ether extract and GE. Addition of SBO also increased (P < 0.05) DE and NE of diets, but had no effect on the DE and NE of corn. Finishing pigs had greater (P < 0.05) growth performance and retention of energy, protein, and lipids than growing pigs. A greater (P < 0.05) DE and NE of diets was observed for finishing pigs than for growing pigs and the DE and NE of corn was also greater (P < 0.05) for finishing pigs than for growing pigs. In conclusion, addition of SBO increases the DE and NE of diets but has no impact on the DE and NE of corn. Diets fed to finishing pigs have greater DE and NE values than diets fed to growing pigs and the DE and NE of corn are greater for finishing pigs than for growing pigs.

Health beneficial long chain omega-3 fatty acid levels in Australian lamb managed under extensive finishing systems

The variation in levels of the health claimable long chain omega-3 fatty acids, eicosapentaenoic acid (EPA, 20:5n-3) plus docosahexaenoic acid (DHA, 22:6n-3) across production regions of Australia was studied in 5726 lambs over 3years completed in 87 slaughter groups. The median level of EPA plus DHA differed dramatically between locations and sometimes between slaughters from the same location. The ratio of EPA plus DHA from lambs with high values (97.5% quantile) to lambs with low values (2.5% quantile) also differed dramatically between locations, and between slaughters from the same location. Consistency between years, at a location, was less for the high to low value ratio of EPA plus DHA than for the median value of EPA plus DHA. To consistently obtain high levels of omega-3 fatty acids in Australian lamb, there must be a focus on lamb finishing diets which are likely to need a supply of α-linolenic acid (18:3n-3), the precursor for EPA and DHA.

Effects of dietary soybean hulls and wheat middlings on body composition, nutrient and energy retention, and the net energy of diets and ingredients fed to growing and finishing pigs1

The objectives of this experiment were 1) to determine the effect of dietary soybean hulls (SBH) and wheat middlings (WM) on body composition, nutrient and energy retention, and the NE of diets and ingredients fed to growing or finishing pigs and 2) to determine if finishing pigs use the energy in SBH and WM more efficiently than growing pigs. Forty growing barrows (initial BW: 25.4 ± 0.7 kg) and 40 finishing barrows (initial BW: 84.8 ± 0.9 kg) were randomly allotted to 5 groups within each stage of growth. Two groups at each stage of growth served as the initial slaughter group. The remaining pigs were randomly assigned to 3 dietary treatments and harvested at the conclusion of the experiment. The basal diet was based on corn and soybean meal and was formulated to be adequate in all nutrients. Two additional diets were formulated by mixing 70% of the basal diet and 30% SBH or 30% WM. In the growing phase, ADG, G:F, and retention of lipids were greater (P < 0.05) for pigs fed the basal diet than for pigs fed the diets containing SBH or WM. Retention of energy was also greater (P < 0.05) for pigs fed the basal diet than for pigs fed the SBH. In the finishing phase, pigs fed the SBH diet tended (P = 0.10) to have a greater ADG than pigs fed the WM diet, and energy retention was greater (P < 0.05) for pigs fed the basal diet than for pigs fed the WM diet. The NE of the basal diet fed to growing pigs was greater (P < 0.01) than the NE of the diets containing SBH or WM, and there was a tendency for a greater (P = 0.05) NE of the basal diet than of the other diets when fed to finishing pigs. The NE of SBH did not differ from the NE of WM in either growing or finishing pigs, and there was no interaction between ingredients and stage of growth on the NE of diets or ingredients. The NE of diets for growing pigs (1,668 kcal/kg) was not different from the NE of diets for finishing pigs (1,823 kcal/kg), and the NE of the diets containing SBH (1,688 kcal/kg) was not different from the NE of the diets containing WM (1,803 kcal/kg). Likewise, the NE of SBH (603 kcal/kg) did not differ from the NE of WM (987 kcal/kg). In conclusion, inclusion of 30% SBH or WM decreases the performance and nutrient retention in growing pigs but has little impact on finishing pigs. The NE of the diets decreases with the inclusion of SBH and WM, but the NE of diets and ingredients is not affected by the BW of pigs. The NE of SBH is not different from the NE of WM.

Macromineral requirements for the maintenance and growth of Boer crossbred kids 1

Advances in mineral nutrition of goats have been made during the last decade, especially in our understanding of Ca and P requirements. However, few studies have focused on the mineral requirements of crossbred Boer goats in their growth phase. Our objective for this study was to determine the macromineral (Ca, P, Mg, K, and Na) requirements for the maintenance and growth of intact, male three-fourths Boer × one-fourth Saanen kids (n = 34; 20.5 ± 0.24 kg of initial BW). Two trials were conducted: 1 for maintenance and 1 for growth requirements. In the maintenance trial, 28 kids were used. The baseline (BL) group consisted of 7 randomly selected kids averaging 21.2 ± 0.36 kg BW and 122 d old. The remaining kids (n = 21; age 168 ± 5 d) were randomly allocated into 7 slaughter groups (blocks) including 3 animals distributed among 3 amounts of DMI (treatments: ad libitum and restricted to 70 or 40% of ad libitum intake). Animals in a group were slaughtered when the ad libitum-treatment kid in the block reached 35 kg BW. The BL and ad libitum-fed groups in the maintenance trial were also part of the growth trial. Therefore, in the growth trial, 20 kids fed for ad libitum intake were used as follows: 7 kids slaughtered at 21.2 ± 0.36 kg BW (BL), 6 kids slaughtered at 28.2 ± 0.39 kg BW (intermediate slaughter), and 7 kids slaughtered at 35.6 ± 0.36 kg BW. Empty whole bodies of the kids (head + feet, hide, internal organs + blood, and carcass) were weighed, ground, mixed, and subsampled for chemical analyses. Daily maintenance requirements, calculated using the comparative slaughter technique (P < 0.001), were estimated as 32.3 ± 1.1 mg Ca, 30.8 ± 1.2 mg P, 1.31 ± 0.5 mg Mg, 8.41 ± 3.0 mg K, and 5.14 ± 1.0 mg Na/kg of empty BW (EBW). Net requirements for growth increased from 6.2 to 6.6 g Ca, 5.3 to 5.4 g P, and 0.29 to 0.30 g Mg and decreased from 1.20 to 1.07 g K and 0.65 to 0.59 g Na/kg of EBW gain for kids from 20 to 35 kg BW. This study indicated that the net mineral requirements for Boer crossbred goat kids may be different from those of purebred or other genotypes, and more data are needed for goats in general.

Fatty acid composition of muscle in Krškopolje pigs and hybrids 12

The aim of the study was to investigate the fatty acids composition of m. longissimus dorsi (LD) in Krškopolje pigs (KP) and maternal hybrids (H12; dam – Slovenian Landrace – line 11, sire – Slovenian Large White). A total of 48 fatteners, 24 of each genotype, were housed in eight pens with six animals in each. They were penned according to genotype and sex. Rearing and feeding conditions were the same for all animals. Pigs were slaughtered in two age groups (G1 and G2) with a two month difference. Twenty-four hours after slaughter, LD samples were taken behind the last rib. Intramuscular fat (IMF) content and fatty acid composition were determined. Statistical analysis was carried out using the GLM procedure in the statistical package SAS/STAT. With IMF content increased saturated fatty acids (SFA), C16:0, monounsaturated fatty acids (MUFA), C16:1n-6 and C18:1n-9 increased with greater IMF content while polyunsaturated fatty acids (PUFA), n-6 PUFA, C18:2n-6, C20:4n-6, n-3 PUFA, ratio PUFA/SFA, and n-6/n-3 decreased with IMF. Gilt’s meat had lower n-6/n-3 ratio than barrow meat. In comparison with H12, KP contained more n-3 PUFA and C18:3n-3 and less C20:4n-6. Additionally, the n-6/n-3 ratio was more desirable in KP meat, indicating a better nutritional meat quality of KP than H12. Muscle of fatteners from the first age group (G1) contained more SFA and C16:0 than from the second age group (G2). Less C20:4n-6 and n-3 PUFA were found in G1 than in G2 which is not desirable from a nutritional point of view. Moreover, trends for better PUFA/SFA and n-3/n-6 were obtained in G1 in comparison with G2. Interaction between the genotype and the slaughter group showed the highest content of C18:3n-3 and the lower ratio n-3/n-6 in younger KP.

Characterizing growth and carcass composition differences in pigs with varying weaning weights and postweaning performance1

The unprecedented increase in litter size over the last decade has led to a perceived increase in the number of fallback pigs (Sus scrofa). However, there is little peer-reviewed data available regarding the biological differences between fallback pigs and their normal cohorts. Therefore, the objective of this experiment was to identify differences in the biology and physiology, and thus the growth and metabolism, between pigs with varying weaning weights (WW) and postweaning performance. To accomplish this objective, a total of 120 barrows (PIC C22/C29 × 337) were used in growth and comparative slaughter experiments. Pigs were selected from a population of 960 weanling pigs to represent the 10% lightest, median, and heaviest pigs at weaning (n = 40 pigs per WW category). Eight pigs from each WW category were harvested on d 5 postweaning as the initial slaughter group (ISG). The remaining 96 barrows were housed in individual crates, fed ad libitum quantities of a common diet during a 27-d growth study, and were harvested on d 33 or 34 postweaning. After the completion of the live animal component of the experiment, pigs within each WW category were further stratified into the slowest, median, or fastest 33% ADG categories. This resulted in a total of 9 treatments in a nested design. Fallback pigs were designated as those belonging to the slowest ADG category from either the lightest or median WW categories. Data were analyzed using the GLIMMIX procedure of SAS with the fixed effects of WW category and WW(ADG). Although feed intake was maximized (P < 0.0001) by WW(ADG) category, feed efficiency was not different (P = 0.30). When equalized per unit of BW, WW(ADG) category greatly affected (P < 0.02) eviscerated carcass, organ, and metabolic BW, but not (P = 0.28) empty BW. There were no differences (P > 0.12) in tissue nutrient concentrations, ratios, or energy content among pigs in the growth experiment. All tissue deposition rates, which were calculated as the difference between tissue nutrient concentrations of the growth experiment and initial slaughter groups, were maximized (P < 0.0002) by WW(ADG), even when equalized per unit of BW. In conclusion, WW and ADG affect tissue accretion rates, but not feed efficiency or carcass composition in nursery pigs.