Injection of conjugated linoleic acid into beef strip loins.

Beef strip loins (IMPS 180; n=15) were sectioned in thirds and sections (n=45) were left untreated (CNT) or injected with either a commercial powder conjugated linoleic acid (CLA) source (Powder) or a commercial oil CLA source (Oil), whose major isomers were 18:2cis-9, trans-11 and 18:2trans-10, cis-12 CLA isomers. Fresh Oil steaks had 3.20 and 3.15, Powder steaks had 4.67 and 4.62, and CNT steaks had 0.19 and 0.02mg/g muscle tissue (wet basis) of the cis-9, trans-11 and trans-10, cis-12 CLA isomers, respectively. TBARS were similar (Oil) and lower (Powder), compared to CNT. Powder steaks had similar instrumental color, and beef and off flavor characteristics as CNT. Artificial marbling was created with Oil steaks having USDA Small(79) and Powder steaks having USDA Modest(86) marbling scores, while CNT steaks had USDA Slight(94) marbling scores. Injection of CLA can be effective in significantly increasing CLA and potentially creating artificial marbling.

Effect of dietary chromium-L-methionine on glucose metabolism of beef steers.

Thirty-six crossbred steers (288 +/- 3.7 kg initial BW) were used to determine the effect of Cr, as chromium-L-methionine, on glucose tolerance and insulin sensitivity in beef calves. Calves were fed a control diet or the diet supplemented with 400 or 800 microg Cr/kg of diet as chromium-L-methionine. Calves were kept in drylots (six calves/pen; two pens/dietary treatment). Steers were caught twice a day in locking headgates and individually fed their respective diets for a period of 22, 23, or 24 d prior to the metabolic challenges. Calves received a totally mixed diet containing 54% corn, 38% cottonseed hulls, and 5% soybean meal. On d 21, 22, and 23, four calves/dietary treatment were fitted with an indwelling jugular catheter. Approximately 24 h after catheterization, an intravenous glucose tolerance test (500 mg glucose/kg of BW), followed 5 h later by an intravenous insulin challenge test (0.1 IU insulin/kg of BW), was conducted. There was no effect (P > 0.10) of dietary treatment on ADG or ADFI. During the intravenous glucose tolerance test, serum insulin concentrations were increased by supplemental chromium-L-methionine (linear effect of Cr, P < 0.05). There was a time x treatment interaction (P < 0.05) on plasma glucose concentrations after the glucose infusion. Plasma glucose concentrations of calves fed 400 microg Cr/kg of diet were lower than those of controls and calves supplemented with 800 microg Cr/kg of diet (quadratic effect of Cr, P < 0.05) 5 and 10 min after the glucose infusion. Supplemental chromium-L-methionine increased the glucose clearance rate from 5 to 10 min after the insulin challenge test (linear effect of Cr, P < 0.05). Glucose half-life from 5 to 10 min after the insulin infusion was also decreased by supplemental chromium-L-methionine (linear effect of Cr, P < 0.10). These data indicate that supplemental Cr, as chromium-L-methionine, increased glucose clearance rate after an insulin infusion and increased the insulin response to an intravenous glucose challenge in growing calves with functioning rumens.

Feed intake, digestibility, and live weight gain by cattle consuming forage supplemented with rice bran and(or) corn.

Effects of supplementing cattle consuming forage with rice bran and(or) corn on feed intake, digestibility, and live weight gain were determined. Holstein steer calves (176 +/- 4.3 kg average trial BW), in two simultaneous 4 x 4 Latin squares, had ad libitum access to bermudagrass or ryegrass-wheat hay without supplementation (Control) or with (DM basis) .5% of BW of ground corn (C), .64% of BW of rice bran (R), or .25% of BW of corn plus .32% of BW of rice bran (CR). Total OM intake with bermudagrass diets was less for R than for C, but values for R and C were not different with ryegrass-wheat (forage source x supplement type interaction; P < .05). An interaction (P < .06) between supplement type and forage source also occurred in digestible OM intake (3.33, 3.66, 2.93, 3.37, 3.77, 4.04, 3.73, and 3.94 kg/d for Control, C, R, and CR with bermudagrass and ryegrass-wheat, respectively). Mature beef cows (504 +/- 25.5 kg BW), in a 6 x 6 Latin square, were limit-fed ryegrass-wheat and alfalfa hay (3:1; air-dry basis) without supplementation (Control) or with (DM basis) .2 or .4% of BW of ground corn (L-C and H-C), .26 or .52% of BW of rice bran (L-R and H-R), or .2% of BW of corn plus .26% of BW of rice bran (H-CR). Duodenal flows of total (125, 122, 123, 137, 136, and 129 g/d) and microbial N (63.3, 64.7, 64.8, 70.3, 73.1, and 65.1 g/d for Control, L-C, H-C, H-R, and H-CR, respectively) were greater (P < .05 and .06, respectively) for rice bran than for corn supplements. Crossbred beef steers (96; 235 +/- 3.2 kg initial BW) of two frame sizes, with half treated with an estrogenic growth promotant, grazed fescue-clover and received Control, L-C, H-C, L-R, H-R, and H-CR supplements for 84 d. Supplement amounts were 50% greater relative to BW than in the preceding experiment. Overall ADG was increased (P < .05) by supplementation and was affected (P < .05) by a supplement type x level interaction (.71, .76, .97, .85, .76, and .94 kg/d for Control, L-C, H-C, L-R, H-R, and H-CR, respectively). Neither frame size nor growth implant modified effects of supplement treatments on ADG.

Digestion, feed intake, and live weight gain by cattle consuming bermudagrass and supplemented with different grains.

The objectives of this study were to determine whether type of supplemental cereal grain, with a relatively high level of supplementation, affects feed intake, characteristics of digestion, and live weight gain by cattle consuming bermudagrass (BER). In Exp. 1, five beef steers (423 +/- 22 kg average BW) with cannulas in the rumen and duodenum were used in a Latin square design experiment. Steers consumed BER hay (1.5% BW; 10.1% CP, 75% NDF, and 6% ADL) alone (Control) or with approximately .7% BW (DM) of ground corn (GC), whole corn (WC), ground sorghum grain (SG), or ground wheat (W). At 8 h after supplementation, ruminal pH was lower for W than for Control, WC, and SG (P < .05). True ruminal OM digestion was lowest for SG and highest for W (P < .05; 49.4, 50.7, 51.0, 42.0, and 57.3% for Control, GC, WC, SG, and W, respectively). In Exp. 2, five Holstein steer calves (187 +/- 9 kg average BW) were used in a Latin square design. Bermudagrass hay (9.7% CP, 72% NDF, and 6% ADL) was consumed ad libitum alone (Control) or with approximately 1% BW of grain (same as in Exp. 1). Digestible OM intake was similar among grain treatments. In Exp. 3, 96 crossbred beef steers (256 +/- 2 kg initial BW) grazed BER (clipped forage samples: 13 to 16% CP, 68 to 73% NDF, and 4 to 5% ADL) for 85 d and received the same grain treatments as in Exp. 2 plus a barley (B) treatment. Live weight gain was .47, .84, .80, .68, .81, and .51 kg/d for Control, GC, WC, B, SG, and W, respectively (SE = .028). In conclusion, when growing cattle grazing BER were supplemented once daily with grain at approximately 1.0% BW, grain that degraded in the rumen slowly (GC, WC, and SG) resulted in live weight gain greater than that resulting from grain that degraded rapidly (B and W).

Feed intake and digestibility by cattle consuming bermudagrass or orchardgrass hay supplemented with soybean hulls and(or) corn.

Effects of supplementing cattle consuming tropical or temperate grass with corn and (or) soybean hulls on feed intake and digestibility were determined. In Exp. 1, eight Holstein steer calves (210 +/- 9.2 and 269 +/- 9.4 kg initial and final BW, respectively), in two simultaneous Latin squares, were given ad libitum access to bermudagrass (B) or orchardgrass (O) hay without supplementation or with (DM basis) .5% of BW of ground corn (C), .7% of BW of soybean hulls (H), or .25% of BW of corn plus .35% of BW of soybean hulls (CH). Total OM intake was greater (P < .05) with than without supplementation (5.05, 6.04, 5.95, 6.06, 6.04, 6.81, 6.61, and 6.69 kg/d), and digestible OM intake was affected by forage source (P < .05), mixing of supplement types (CH versus the mean of C and H; P < .09), and the forage source x supplementation interaction (P < .09; 2.65, 3.40, 3.33, 3.46, 3.71, 4.14, 3.98, and 4.30 kg/d for B, B-C, B-H, B-CH, O, O-C, O-H, and O-CH, respectively). Total tract NDF digestibility was greater (P < .05) for O than for B diets and for H than for C (56.4, 53.9, 58.1, 56.9, 68.5, 64.9, 67.7, and 69.6% for B, B-C, B-H, B-CH, O, O-C, O-H, and O-CH, respectively). In Exp. 2, mature cannulated beef cattle (524 +/- 1.6 kg BW) were used in a design similar to Exp. 1 with comparable dietary supplement levels.(ABSTRACT TRUNCATED AT 250 WORDS)

Digestion, feed intake, and live weight gain by cattle consuming bermudagrass hay supplemented with whey.

Three experiments were conducted with cattle consuming bermudagrass hay to determine whether low-level supplements of whey alone, corn alone, or whey plus corn affect feed intake, digestion, and(or) BW gain. Six ruminally and duodenally cannulated beef cows (574 kg), used in a Latin-square trial (Exp. 1), were fed bermudagrass hay without supplementation (control) or with 2.8% whey (low whey, LW), 5.6% whey (high whey, HW), 17.4% ground corn (C), 2.8% whey plus 14.9% corn (C-LW), or 5.6% whey plus 12.4% corn (C-HW). Supplementing with whey and(or) corn increased ruminal butyrate (8.8, 9.4, 10.0, 9.6, 10.5, and 11.0 mol/100 mol of total VFA for control, LW, HW, C, C-LW, and C-HW, respectively; SE = .20). Supplements did not affect microbial N flow at the duodenum. Six Holstein steer calves (158 kg) in a Latin square (Exp. 2) consumed bermudagrass hay ad libitum alone (control) or with .075 or .15% BW whey (LW and HW, respectively), .5% BW ground corn (C), or corn-whey mixes made by substituting whey for corn (C-LW and C-HW). Substituting .15% BW of whey for corn increased (P less than .05) total OM intake slightly (3.99, 3.84, 3.75, 4.11, 4.28, and 4.47 kg for control, LW, HW, C, C-LW, and C-HW, respectively; SE = .10). In an 84-d randomized block experiment (Exp. 3), 96 beef calves (194 kg) consumed (ad libitum) low-quality bermudagrass hay alone or with C, LW, HW, C-LW, or C-HW supplements.(ABSTRACT TRUNCATED AT 250 WORDS)

Effects of animal and supplement characteristics on average daily gain of grazing beef cattle.

Effects of animal gender and age, use of a growth stimulant, and supplementation with grain alone or grain plus other substances on ADG by growing beef cattle grazing bermudagrass paddocks with sod-seeded rye, wheat, and ryegrass were determined. Two grazing experiments (Exp. 1: late winter through mid-spring; Exp. 2: late spring through mid-summer) were conducted. Experiment 1 used 96, 12- to 13-mo-old Simmental-cross calves (heifers, 240 kg; steers, 272 kg), half of which were implanted with zeranol. Within each implant treatment, cattle received no supplement or .5% BW (DM) of ground corn alone or plus a mix of protein meals, zinc sulfate, thiamin-HCl, or salt. Daily gain was higher (P less than .05) with than without supplementation and was similar (P greater than .10) among supplement treatments. In Exp. 2, 96 crossbred beef steers, approximately 7 (230 kg) or 15 mo old (250 kg), were not supplemented (control) or received .5% BW (DM) of ground corn on d 1 to 84 (C-C), corn plus a protein meal mix on d 1 to 84 (CP-CP), corn on d 43 to 84 (O-C), corn plus the protein meal mix on d 43 to 84 (O-CP), or corn on d 1 to 42 and corn plus the protein meal mix on d 43 to 84 (C-CP). Daily gain on d 1 to 84 was affected (P less than .05) by supplement, age, implant, and the supplement x implant interaction (nonimplanted: .37, .56, .68, .40, .49, and .49; implanted: .37, .62, .54, .49, .70, and .71 kg for control, C-C, CP-CP, O-C, O-CP, and C-CP, respectively).

Relationships of body weight, forage composition, and corn supplementation to feed intake and digestion by Holstein steer calves consuming bermudagrass hay ad libitum.

Holstein steer calves (101 to 350 kg BW) consumed bermudagrass hay ad libitum without or with supplemental ground corn up to 1.0% of BW. As BW increased, total DMI increased quadratically (-2.459 + .05448 [BW]-.000073 [BW2] + .540 [corn DMI]; R2 = .83, sy.x = .655). Each kilogram of corn DM decreased bermudagrass DMI by .46 kg. Total digestible OM intake (kg) increased with BW and corn supplementation (.314 + .0127 [BW] + .441 [corn OM intake]; R2 = .79, sy.x = .444). Feed intake level accounted for approximately 2.5 times more variability in total digestible OM intake than digestion did. Corn supplementation decreased digestion of bermudagrass NDF (62.50 - 8.468 [corn DMI, % BW]; R2 = .13, sy.x = 8.121), with a similar decrease across BW. Increasing bermudagrass DMI (% of BW) decreased bermudagrass NDF digestion slightly, but variation accounted for was only 33% of that attributable to corn DMI (% of BW). Concentrations of common fiber fractions (NDF, ADF, cellulose, hemicellulose, and ADL) in bermudagrass explained very little variation in feed intake and digestion, indicating considerable influence of other factors. Bermudagrass intake and digestion were not related, and no substantial interactions were observed among steer BW, corn level, and bermudagrass composition.

Alternating dietary fat sources for growing-finishing pigs fed dried distillers grains with solubles: I. Growth performance, pork carcass characteristics, and fatty acid composition of subcutaneous fat depots.

Crossbred pigs (n = 216) were used to test the effects of phase-feeding beef tallow (BT) and yellow grease (YGr) on live performance, carcass characteristics, and fatty acid composition of subcutaneous (s.c.) fat depots of growing-finishing swine. Pigs were blocked by initial BW (26.0 ± 5.3 kg) before allotment to pens (6 pigs/pen), and pens (6 pens/block) were assigned randomly to 1 of 6 dietary treatments: 1) corn-soybean meal-based grower and finisher diets formulated with 4.7% YGr fed during all 5 feeding phases (YG15), 2) corn-soybean meal-based diets formulated with 5.0% BT fed during all 5 phases (BT15), 3) diets containing 5.0% BT fed during the first 2 phases and diets with 4.7% YGr fed the last 3 phases (YG345), 4) diets formulated with 5.0% BT fed during first 3 phases and diets containing 4.7% YGr fed during the last 2 phases (YG45), 5) diets containing 4.7% YGr fed during the first 3 phases and diets with 5.0% BT fed during the last 2 feeding phases (BT45), or 6) diets formulated with 4.7% YGr fed during the first 2 phases and diets with 5.0% BT fed during the last 3 phases (BT345). Overall performance was similar (P ≥ 0.06) among dietary treatments; however, overall ADG and ADFI increased (quadratic, P ≤ 0.05) with increasing days fed BT, but duration of dietary YGr did not affect ADG (P ≥ 0.22) or ADFI (P ≥ 0.30). There was no (P ≥ 0.23) effect of fat inclusion on carcass characteristics, but carcass lean yield decreased (linear, P = 0.02) as duration of YGr feeding increased from 37 to 103 d. Proportions of back fat SFA (quadratic, P = 0.03) and jowl fat MUFA (linear, P = 0.02) increased as the time fed BT increased from 47 to 103 d. Conversely, PUFA content of both s.c. fat depots increased (linear, P < 0.01) with increasing durations of dietary YGr. Moreover, quadratic slopes for linolenic (18:2n-6) and linolenic (18:3n-3) acids in jowl fat differed (P ≤ 0.05) between BT and YGr durations, indicating that the percentages of 18:2n-6 and 18:3n-3 increased at a greater rate with increasing time fed YGr than the rate of decreases in 18:2n-6 and 18:3n-3 associated with increasing time fed BT. Results of this study confirm that the fatty acid composition of s.c. fat depots are similar to that of the dietary fat source fed during the last 2 or 3 feeding phases, yet deposition rates of specific fatty acids appear to be dependent on the length of time pigs are fed a specific fat source.

Alternating dietary fat sources for growing-finishing pigs fed dried distillers grains with solubles: II. Fresh belly and bacon quality characteristics.

Crossbred pigs (n = 216) were used to test the effects of phase-feeding beef tallow (BT) and yellow grease (YGr) on fresh belly and bacon quality characteristics of growing-finishing swine fed dried distillers grains with solubles (DDGS). Pigs were blocked by initial BW (26.0 ± 5.3 kg) before allotment to pens (6 pigs/pen), and pens (6 pens/block) were assigned randomly to 1 of 6 dietary treatments: 1) corn-soybean meal-based grower and finisher diets formulated with 4.7% YGr fed during all 5 feeding phases (YG15); 2) corn-soybean meal-based diets formulated with 5.0% BT fed during all 5 phases (BT15); 3) diets containing 5.0% BT fed during the first 2 phases and diets with 4.7% YGr fed the last 3 phases (YG345); 4) diets formulated with 5.0% BT fed during first 3 phases and diets containing 4.7% YGr fed during the last 2 phases (YG45); 5) diets containing 4.7% YGr fed during the first 3 phases and diets with 5.0% BT fed during the last 2 feeding phases (BT45); or 6) diets formulated with 4.7% YGr fed during the first 2 phases and diets with 5.0% BT fed during the last 3 phases (BT345). All dietary treatments were formulated with 30% dried distillers grains with solubles (DDGS) during the first 3 phases, 15% DDGS in the fourth phase, and no DDGS during the last phase. Fresh belly quality data were collected on the left-side bellies, whereas bacon from the right-side bellies was prepared under commercial processing conditions. Additionally, USDA-certified No. 1 slices were collected for cooking characteristics and sensory panel evaluations. Bellies from the YG15-fed pigs were softer (P ≤ 0.05) than bellies from BT15-fed pigs; however, instrumentally measured belly firmness was not (P ≥ 0.06) different among treatments. Concentrations of palmitic, stearic, and oleic acids, as well as all SFA and all MUFA, were greater (P < 0.01) in bellies from BT15- than YG15-fed pigs. In contrast, proportions of linoleic acid, all PUFA, and iodine value were greater (P < 0.01) in belly fat from YG15-fed pigs in comparison with BT15-fed pigs. Yield of commercially processed bacon (P ≥ 0.06), mechanical bacon tenderness (P ≥ 0.69), and bacon palatability attributes (P ≥ 0.55) were not affected by the dietary treatments. Thus, results of this study indicated that phase-feeding BT to pigs fed diets formulated with DDGS produced minor improvements in fresh belly firmness due to greater proportions of SFA but had no effect on yields of commercially processed bacon or bacon quality characteristics.

Effects of conjugated linoleic acid, salt, and sodium tripolyphosphate on physical, sensory, and instrumental color characteristics of beef striploins.

USDA Select striploins (IMPS 180; n= 24) were cut into thirds (anterior, medial, and posterior) and assigned to 1 of 8 treatments utilizing a randomized incomplete block design. Treatments included (1) control (C); (2) 1.5% conjugated linoleic acid (conjugated linoleic acid = CLA) (CGA); (3) 0.4% sodium tripolyphosphate (PHO); (4) 0.5% salt (SAL); (5) 0.4% sodium tripolyphosphate, 0.5% salt (SPH); (6) 0.4% sodium tripolyphosphate, 1.5% CLA (PCL); (7) 0.5% salt, 1.5% CLA (SCL); and (8) 0.4% sodium tripolyphosphate, 0.5% salt, 1.5% CLA (SPC). Treatments were injected with solutions to 110% (10% pump) of their original weight. Treatments with CLA had higher (P < 0.05) marbling scores than treatments that did not. Not including SAL, treatments with salt, or phosphate or a combination of the two had higher tenderness values when sampled by panelists. Fresh steaks with inclusion of CLA had greater amounts (P < 0.05) of the CLA isomers than steaks not having CLA. Cooked steaks having CLA also had greater amounts (P < 0.05) of CLA, except for SCL, which were not different (P > 0.05) from the non-CLA treatments. Day was a significant source of variability for a*, b*, and saturation index. Treatment x day interactions were significant (P < 0.05) for hue angle and L* values. These data suggest that inclusion of CLA can increase amounts of CLA isomers without major deleterious effects to instrumental, physical, and quality characteristics of beef striploin steaks.

Interactive effects of dietary fat source and slaughter weight in growing-finishing swine: I. Growth performance and longissimus muscle fatty acid composition.

Crossbred pigs (n=288) were used to test the interactive effects of dietary fat source and slaughter weight on live performance, carcass traits, and fatty acid composition of the LM. Pigs were blocked by initial BW, and, within each of 9 blocks, pens (8 pigs/pen) were randomly assigned to either control corn-soybean meal grower and finisher diets devoid of added fat (Ctrl) or diets formulated with 5% beef tallow (BT), poultry fat (PF), or soybean oil (SBO). Immediately after treatment allotment, as well as at mean block BW of 45.5, 68.1, 90.9, and 113.6 kg, 1 pig was randomly selected from each pen, slaughtered, and allowed to chill for 48 h at 1 degrees C. Backfat was measured on the right sides, and a sample of the LM was removed for fatty acid composition analysis. Regardless of source, inclusion of fat in swine diets did not (P >or= 0.349) affect ADG, ADFI, or G:F. Furthermore, carcasses from pigs fed diets formulated with 5% fat had greater (P=0.013) average backfat depths than those from pigs fed the Ctrl diet. Body weight, carcass weight, and backfat depths increased (P<0.001) as slaughter weight increased from 28.1 to 113.6 kg. The proportion of SFA in the LM increased (P<0.001) with increasing slaughter weight from 28.1 to 68.1 kg, but SFA percentages were similar between 68.1 and 113.6 kg, and pigs fed the Ctrl diet had greater (P=0.032) proportions of SFA than pigs fed the SBO and PF diets. Moreover, the proportion of all MUFA increased (P<0.001) by 9.4 percentage units from 28.1 to 113.6 kg; however, only pigs fed the SBO diet had reduced (P=0.004) MUFA percentages than those fed the Ctrl, BT, and PF diets. Even though the proportion of PUFA in the LM decreased with increasing slaughter weight, pigs fed SBO had greater PUFA percentages, a greater PUFA-to-SFA ratio, and greater iodine values than pigs fed all other dietary treatments when slaughtered at BW of 45.5 kg or greater (fat source x slaughter weight, P < 0.001). Results of this study indicate that fat source had little to no impact on live pig performance, but feeding a polyunsaturated fat source altered the fatty acid profile of the LM within the first 17.4 kg of BW gain; more specifically, including 5% SBO in swine diets could lead to economical ramifications associated with soft pork or fat.

Interactive effects of dietary fat source and slaughter weight in growing-finishing swine: II. Fatty acid composition of subcutaneous fat.

Crossbred pigs (n=288) were used to test the interactive effects of dietary fat source and slaughter weight on the fatty acid composition of subcutaneous fat. Pigs were blocked by initial BW (28.1 kg), and, within blocks, pens (8 pigs/pen) were randomly assigned to either grower and finisher diets devoid of added fat (Ctrl) or diets formulated with 5% beef tallow (BT), poultry fat (PF), or soybean oil (SBO). Immediately after treatment allotment, as well as at mean block BW of 45.5, 68.1, 90.9, and 113.6 kg, 1 pig was randomly selected from each pen, slaughtered, and, within 1 h postmortem, samples of backfat were removed from each carcass between the 4th and 8th thoracic vertebra and separated into the inner, middle, and outer layers for fatty acid composition analysis. During the first 17.4 kg of BW gain, percentages of all SFA increased by more than 4% in subcutaneous fat of pigs fed the Ctrl and BT diets, but decreased by 4.4 and 7.7% in pigs fed the PF and SBO diets, respectively (fat source x slaughter weight, P<0.001). Proportions of all MUFA in subcutaneous fat from BT-fed pigs increased by 6.1% during the first 17.4 kg of BW gain, but MUFA percentages in SBO-fed pigs decreased by 9.1% between 28.1 and 45.5 kg (fat source x slaughter weight, P<0.001). Conversely, percentages of all PUFA from SBO-fed pigs increased by 39.9%, whereas PUFA concentrations in BT-fed pigs decreased by 12.6% as slaughter weight increased from 28.1 to 45.5 kg (fat source x slaughter weight, P<0.001). Resultant iodine values (IV) of subcutaneous fat from SBO-fed pigs increased (P<0.05) from 73.5 to 85.2 within the first 17.4 kg of BW gain, and remained elevated above those of their contemporaries fed the Ctrl, BT, or PF diets at each subsequent slaughter weight (fat source x slaughter weight, P<0.001). The inner backfat layer had the greatest (P<0.05) proportions of all SFA and the least (P<0.05) proportions of all PUFA, whereas the outer layer had the least (P<0.05) percentages of all SFA but the greatest (P<0.05) percentages of all MUFA. Even though the middle and outer subcutaneous fat layers had similar (P>0.05) PUFA percentages, the greatest (P<0.05) and least (P<0.05) IV were in the outer and middle layers, respectively. As expected, the fat source included in swine diets was responsible for the fatty acid compositional changes in subcutaneous fat, yet the results of this study indicate that feeding 5% SBO dramatically increased the polyunsaturation of subcutaneous fat within the first 17.4 kg of BW gain, with backfat IV exceeding 80 thereafter.

Interactive effects of dietary fat source and slaughter weight in growing-finishing swine: III. Carcass and fatty acid compositions.

Crossbred pigs (n=288) were used to test the interactive effects of dietary fat source and slaughter weight on dissected carcass composition and fatty acid composition of composite carcass samples. Pigs were blocked by initial BW, and within each of 9 blocks, pens (8 pigs/pen) were randomly assigned to either control corn-soybean meal grower and finisher diets (Ctrl) or diets formulated with 5% beef tallow (BT), poultry fat (PF), or soybean oil (SBO). Immediately after treatment allotment, as well as at mean block BW of 45.5, 68.1, 90.9, and 113.6 kg, 1 pig was randomly selected from each pen and slaughtered, and primal cuts from right carcass sides were dissected into muscle, fat, bone, and skin components. Muscle and fat tissues were then ground, and random composite samples were collected from each carcass for fatty acid composition analysis. Fat source did not alter pork primal cut yields (P >or= 0.294), nor were the percentages of carcass muscle (P=0.213), fat (P=0.502), and bone (P=0.551) affected by dietary fat source. Conversely, percentages of the whole shoulder and ham decreased linearly (P<0.001), and the percentages of loin and belly increased (P<0.001) linearly with increasing slaughter weight. Moreover, linear decreases (P<0.001) in carcass muscle, bone, and skin, as well as a linear increase (P<0.05) in carcass fat, were observed as slaughter weight increased from 28.1 to 113.6 kg. Composite samples from pigs fed the BT or Ctrl diets had greater (P<0.05) proportions of SFA, particularly oleic and stearic acids, than those from pigs fed the PF and SBO diets when slaughtered at 45.5, 68.1, and 90.9 kg (fat source x slaughter weight, P<0.001). Percentages of MUFA (including palmitoleic, oleic, and cis-vaccenic acids) decreased (P<0.05), and percentages of all PUFA, especially linoleic and linolenic acids, and iodine values increased (P<0.05) in samples from SBO-fed pigs as slaughter weight increased from 28.1 to 113.6 kg (fat source x slaughter weight, P<0.001). Dietary fat source did not affect carcass composition; however, including 5% SBO in swine diets increased the polyunsaturation of pork, which could lead to economic ramifications associated with soft pork and pork fat.

Treadmill exercise is not an effective methodology for producing the dark-cutting condition in young cattle.

Holstein steer calves (n = 25) were used to evaluate the effects of treadmill exercise (TME) on blood metabolite status and formation of dark-cutting beef. Calves were blocked by BW (156 +/- 33.2 kg) and assigned randomly within blocks to 1 of 5 TME treatments arranged in a 2 x 2 factorial design (4 or 8 km/h for a duration of 10 or 15 min) with a nonexercised control. Venous blood was collected via indwelling jugular catheters at 10, 2, and 0 min before TME and at 2-min intervals during exercise. Nonexercised steers were placed on the treadmill but stood still for 15 min. Serum cortisol levels, as well as plasma concentrations of glucose, lactate, and NEFA, were similar (P > 0.05) before TME. Serum cortisol concentrations were unaffected (P > 0.05) during the first 6 min of TME, but between 8 and 15 min of TME, cortisol concentrations were greater (P < 0.05) in steers exercised at 8 km/h than those exercised at 4 km/h or controls (speed x time, P < 0.001). Although TME did not affect (P > 0.05) plasma glucose levels, plasma lactate concentrations in steers exercised at 8 km/h increased (P < 0.05) sharply with the onset of the TME treatment and remained elevated compared with steers exercised at 4 km/h or unexercised controls (speed x time, P < 0.001). Exercised steers had the lowest (P < 0.05) plasma NEFA concentrations during the first 6 min of TME compared with unexercised steers; however, NEFA concentrations were similar after 10 and 12 min of TME, and by the end of TME, steers exercised at 8 km/h had greater (P < 0.05) NEFA levels than nonexercised controls or steers exercised at 4 km/h (speed x time, P < 0.001). Even though muscle glycogen levels and pH decreased (P < 0.001) and muscle lactate concentrations increased (P < 0.001) with increasing time postmortem, neither treadmill speed nor TME duration altered postmortem LM metabolism. Consequently, there were no (P > 0.05) differences in the color, water-holding capacity, shear force, or incidences of dark-cutting carcasses associated with preslaughter TME. It is apparent that preslaughter TME, at the speeds and durations employed in this study, failed to alter antemortem or postmortem muscle metabolism and would not be a suitable animal model for studying the formation of the dark-cutting condition in ruminants.

Duration of restraint and isolation stress as a model to study the dark-cutting condition in cattle.

Holstein steer calves (n = 32; 156 +/- 33.2 kg average BW) were used to evaluate the duration of restraint and isolation stress (RIS) on endocrine and blood metabolite status and the incidence of dark-cutting LM. Calves were blocked by BW and assigned randomly within blocks to one of four stressor treatments: unstressed controls (NS) or a single bout of RIS for 2, 4, or 6 h. Venous blood was collected via indwelling jugular catheters at 40, 20, and 0 min before stressor application and at 20-min intervals during RIS. Unstressed calves remained in their home stanchions and, except for blood sampling, were subjected to minimal handling and stress. Serum cortisol and plasma lactate concentrations were increased (P < 0.01) during the first 20 min after RIS application, and remained elevated throughout the 6 h of RIS. Plasma concentrations of glucose and insulin were greater (P < 0.05) in RIS calves than in NS calves after 80 and 100 min of stressor application, respectively; however, RIS did not (P > 0.80) affect plasma NEFA concentrations. Calves were slaughtered within 20 min of completion of RIS, and muscle samples were excised from right-side LM at 0, 0.75, 1.5, 3, 6, 12, 24, and 48 h after exsanguination for quantifying LM pH, and glycogen and lactate concentrations. The pH of the LM from calves subjected to 6 h of RIS exceeded 6.0, and was greater (P < 0.05) at 24 and 48 h postmortem than the pH of NS calves or calves subjected to 2 or 4 h RIS. Muscle glycogen concentrations did not differ (P = 0.16; 25.58, 10.41, 13.80, and 14.41 micromol/g of wet tissue weight for NS and 2-, 4-, and 6-h RIS, respectively), and LM lactate concentrations tended to be lower (P = 0.08) in calves subjected to 6 h of RIS. At 48 h after exsanguination, the LM from calves subjected to 6 h of RIS had more (P < 0.05) bound and less (P < 0.05) free moisture than did the LM from NS calves or calves subjected to 2 or 4 h of RIS. Additionally, the LM from RIS calves was darker (lower L* values; P < 0.05) than the LM of NS calves. Visual color scores for the LM were greatest (P < 0.05) for calves subjected to 6 h of RIS and least (P < 0.05) for NS calves. Subjecting lightweight Holstein calves to 6, 4, and 2 h of RIS resulted in six (75%), two (25%), and two (25%) carcasses characteristic of the dark-cutting condition, respectively. There were no dark-cutting carcasses produced from NS calves. Thus, RIS may be a reliable animal model with which to study the formation of the dark-cutting condition.

Feed intake and digestion by Holstein steers fed warm or cool season grass hays with corn, dried molasses, or wheat middlings.

This study determined the effects of adding a small amount of dried molasses to supplemental corn and of supplementing with corn, wheat middlings, or corn-wheat middlings mixture on intake and digestion by Holstein steers fed warn or cool season grass hays. Eight steers (175 kg BW), in two simultaneous Latin squares, were fed, once daily, bermuda-grass (72% NDF) or ryegrass-wheat (58% NDF) hay ad libitum, alone or with approximately .05% BW of dried molasses (with 31% roughage), 5% BW of ground corn, or both. Adding dried molasses to corn decreased feed intake but did not affect digestible OM intake. Total tract digestion of fiber from bermudagrass tended to be enhanced by adding dried molasses to corn. Eight steers (193 kg BW) were used in an experiment with the same design in which similar forages were fed alone or with corn (.5% BW), wheat middlings (.63% BW), or .25% BW of corn plus .31% BW of middlings. Feed intake for both grasses was similar among supplements. Wheat middlings depressed total tract fiber digestion more than corn with both forages. Supplementation with corn depressed fiber digestion slightly more with ryegrass-wheat than with bermudagrass, but wheat middlings had a slightly greater depressing effect on fiber digestion with bermudagrass. Associative effects of mixing corn and wheat middlings in OM digestion and digestible OM intake were negative for bermudagrass and positive for ryegrass-wheat. Interaction among characteristics of basal forage and concentrate modulated feed intake and digestion by ruminants.

Forage and splanchnic tissue mass in growing lambs: effects of dietary forage levels and source on splanchnic tissue mass in growing lambs.

Forty-two crossbred lambs (33.4 kg initial body weight; twenty-four wethers and eighteen ewes) were used in a 42 d experiment with a 2 x 3 factorial treatment arrangement to determine effects of forage level and source on splanchnic tissue mass. Diets were 250 and 750 g/kg of chopped lucerne (Medicago sativa) (A), ryegrass (Lolium multiflorum)-wheat (Triticum aestivum) (RW) or bermudagrass (Cynodon dactylon) (B) hay, with the remainder being maize-based concentrate. Five lambs per treatment were slaughtered at the end of the experiment and measurements made of internal organs and contents of the gastrointestinal tract (GIT). Digestible organic matter intake (DOMI) on the 7 d preceding slaughter was 0.89, 0.83, 0.90, 0.83, 0.77 and 0.61 (SE 0.05) kg/d, and live-weight gain was 0.20, 0.17, 0.18, 0.10, 0.10 and 0.07 (SE 0.02) kg/d for diets A-25, RW-25, B-25, A-75, RW-75 and B-75 respectively. Total GIT mass (fresh) was higher (P < 0.05) for 750 than 250 g forage/kg and for B than RW (4.80, 4.57, 5.55, 5.84, 5.99 and 6.91 kg for diets A-25, RW-25, B-25, A-75, RW-75 and B-75 respectively). Non-fat organic matter was 259, 295, 292, 303, 277 and 264 g for the total GIT; 93, 102, 103, 106, 95 and 97 g for the reticulo-rumen (forage level x type (diet A v. diets RW and B) interaction; P < 0.05); and 204, 196, 202, 177, 156 and 127 g for the liver (SE 10) with diets A-25, RW-25, B-25, A-75, RW-75 and B-75 respectively. In summary, differences in properties of forage A and the grasses at 250 g/kg diet may have influenced GIT mass independent of energy intake and digesta mass. Conversely, with 750 g dietary forage/kg, higher digesta mass for diet B than diet RW appeared responsible for high reticulo-rumen mass relative to DOMI. Greater digesta mass for 750 than 250 g forage/kg may have elevated intestinal tissue mass/DOMI with diets A and B but not with diet RW, for which NDF digestibility was highest.

Digestion characteristics by beef cattle consuming bermudagrass or bromegrass hay alone or with alfalfa and(or) corn.

Cannulated beef cattle (four cows: 556 kg initial weight; four steers: 504 kg initial weight) were used in an experiment with two simultaneous Latin squares to determine effects of substituting alfalfa and(or) corn for vegetative bermudagrass (BER; 77% neutral detergent fibre and 5.5% acid detergent lignin) or mature bromegrass (BRO; 70% neutral detergent fibre and 6.6% acid detergent lignin) hay on digestion characteristics. For Controls, BER or BRO was fed at 1.32 or 1.54% body weight of cows and steers, respectively; other treatments entailed substitution for hay DM of alfalfa cubes (17%) or ground corn (33%). A protein supplement was given to all animals. In vitro neutral detergent fibre (NDF) digestion was slightly greater for BER than BRO. Supplement treatments did not affect the concentration of total volatile fatty acids or the molar proportion of propionate in ruminal fluid. True ruminal organic matter (OM) digestion was similar among diets; greater duodenal microbial OM flow and postruminal NDF digestion for BRO than BER diets were responsible for higher (P < 0.05) postruminal OM digestion for BRO diets. Supplement treatment did not affect duodenal microbial nitrogen flow or efficiency of microbial growth. Corn supplementation increased total tract OM digestion (P < 0.05). Alfalfa addition depressed total tract OM and NDF digestibilities more when added to BER than BRO; depressions in total tract NDF digestion with alfalfa and corn substitutions were additive. With constant DM intake, slightly less than ad libitum, alfalfa or corn substituted alone or together for hay did not improve characteristics of digestion by cattle consuming vegetative bermudagrass or mature bromegrass other than increased postruminal and total tract OM digestibilities with corn.

Digestion in steers and lactational performance of Jersey cows fed diets varying in natural protein level continuously or on alternate days.

Five crossbred beef steers (515 kg) were used in a Latin square experiment and 36 lactating Jersey cows (12 primiparous, 310 kg; 24 multiparous, 365 kg) were used in a completely randomized design study to determine effects on characteristics of digestion and lactational performance of daily alternation of the dietary level of natural protein (NP). In Experiment 1, steers were fed diets of 50% bermudagrass hay and 50% concentrate. Concentrate was approximately 18% crude protein (CP), formulated to be 60, 80 or 100% NP (varying proportions of soybean meal, urea and ground corn), and was fed at 1.5% body weight (dry matter basis). These concentrates were fed daily or ones with 60 and 100% NP were fed on alternate days. Alternate day feeding did not markedly affect characteristics of digestion, including ruminal escape of feed protein, and NP level of concentrate fed continuously had no effects either. In Experiment 2, cows were subjected to treatments similar to those in Experiment 1, and performance on d 20-40 of lactation was measured. Concentrate was given at 1 kg (as fed)/2.15 kg milk produced, yielding a dietary concentrate level of approximately 40% (dry matter basis). Alternate feeding depressed (P less than 0.05) overall milk fat percentage. Alternate feeding increased production of milk and protein and body weight of primiparous cows but caused little change with multiparous cows. Besides increasing the dietary level of concentrate, perhaps alternate feeding regimes have utility to lower milk fat level without impairing milk production. Level of NP in concentrate fed continuously did not affect performance by multiparous cows though primiparous cow performance was generally enhanced, possibly because CP intake was adequate for multiparous cows but marginal for primiparous cows. However, overall, efficiency of production of solids-corrected milk rose slightly with increasing NP.