Effects of Increasing Dietary Niacin on Weanling Pig Performance

Two experiments using 415 weanling pigs (4.8 ± 0.98 kg and 14 ± 4 d of age) were conducted to determine the effect of increasing dietary niacin on pig performance. Pigs were blocked by BW and randomly allotted to one of five dietary treatments. There were five pigs per pen with seven pens per treatment in Exp. 1, and eight pigs per pen with six pens per treatment in Exp. 2. Diets were fed in four phases (d 0 to 4, 4 to 8, 8 to 22, and 22 to 35). Pigs were fed the control diet with no added niacin or the control diet with 28, 55, 83, or 110 mg/kg of added niacin; data from both trials were combined. From d 0 to 22, increasing niacin had no effect (P>0.10) on growth performance. From d 22 to 35, increasing niacin had no effect (P>0.10) on ADG or ADFI, but improved (linear, P<0.04) gain:feed ratio (G:F). Overall (d 0 to 35), increasing niacin had no affect (P>0.10) on ADG or ADFI, but tended to numerically (linear, P<0.10) improve G:F. In summary, diets high in dried whey and other specialty protein sources appear to contain adequate niacin to maximize growth performance for the first 3 wk after weaning. However, in the late nursery phase (d 22 to 35) when pigs are fed corn-soybean meal diets, up to 110 mg/kg of added niacin linearly (P<0.04) improves G:F.     

Effects of increasing dietary L-carnitine on growth performance of weanling pigs

Four experiments were conducted to evaluate the effects of supplementing graded levels (0 to 100 ppm) of L-carnitine to the diet of weanling pigs on growth performance during a 34- to 38-d experimental period. A fifth experiment was conducted to determine the effects of addition of L-carnitine to diets with or without added soybean oil (SBO) on growth performance. In Exp. 1, 128 pigs (initial BW = 5.5 kg) were allotted to four dietary treatments (six pens per treatment of four to six pigs per pen). Dietary treatments were a control diet containing no added L-carnitine and the control diet with 25, 50, or 100 ppm of added L-carnitine. In Exp. 2, 3, and 4, pigs (4.8 to 5.6 kg of BW) were allotted to five dietary treatments consisting of either a control diet containing no added L-carnitine or the control diet with 25, 50, 75, or 100 ppm of added L-carnitine. All diets in Exp. 1 to 4 contained added soybean oil (4 to 6%). There were seven pens per treatment (four to five pigs per pen) in Exp. 2, whereas Exp. 3 and 4 had five and six pens/treatment (eight pigs per pen), respectively. In general, dietary carnitine additions had only minor effects on growth performance during Phases 1 and 3; however, dietary L-carnitine increased (linear [Exp. 1], quadratic [Exp. 2 to 4], P < 0.03) ADG and gain:feed (G:F) during Phase 2. The improvements in growth performance during Phase 2 were of great enough magnitude that carnitine addition tended to increase ADG (linear, P < 0.10) and improve G:F (quadratic, P < 0.02) for the entire 38-d period. In Exp. 5, 216 weanling pigs (5.8 kg of BW) were allotted (12 pens/treatment of four to five pigs per pen) to four dietary treatments. The four dietary treatments were arranged in a 2 x 2 factorial with main effects of added SBO (0 or 5%) and added L-carnitine (0 or 50 ppm). Pigs fed SBO tended (P < 0.07) to grow more slowly and consumed less feed compared with those not fed SBO, but G:F was improved (P < 0.02). The addition of L-carnitine did not affect (P > 0.10) ADG or ADFI; however, it improved (P < 0.03) G:F. Also, the increase in G:F associated with L-carnitine tended to be more pronounced for pigs fed SBO than those not fed SBO (carnitine x SBO, P < 0.10). These results suggest that the addition of 50 to 100 ppm of added L-carnitine to the diet improved growth performance of weanling pigs. In addition, supplemental L-carnitine tended to be more effective when SBO was provided in the diet.     

Sulfur concentration in diets containing corn, soybean meal, and distillers dried grains with solubles does not affect feed preference or growth performance of weanling or growing-finishing pigs

Four experiments were conducted to investigate the effects of distillers dried grains with solubles (DDGS) and dietary S on feed preference and performance of pigs. In a 10-d feed preference experiment (Exp. 1), 48 barrows (20.1 ± 2.2 kg of BW) were randomly allotted to 3 treatment groups, with 8 replicate pens per treatment and 2 pigs per pen. A control diet based on corn and soybean meal, a DDGS diet containing 20% DDGS, and a DDGS-sulfur (DDGS-S) diet were prepared. The DDGS-S diet was similar to the DDGS diet with the exception that 0.74% CaSO(4) was added to the diet. Two diets were provided in separate feeders in each pen: 1) the control diet and the DDGS diet, 2) the control diet and the DDGS-S diet, or 3) the DDGS diet and the DDGS-S diet. Preference for the DDGS diet and the DDGS-S diet vs. the control diet was 35.2 and 32.6%, respectively (P < 0.05), but there was no difference between the DDGS diet and the DDGS-S diet. In Exp. 2, a total of 90 barrows (10.3 ± 1.4 kg of BW) were allotted to 3 treatments, with 10 replicate pens and 3 pigs per pen, and were fed the diets used in Exp. 1 for 28 d, but only 1 diet was provided per pen. Pigs fed the control diet gained more BW (497 vs. 423 and 416 g/d; P < 0.05) and had greater G:F (0.540 vs. 0.471 and 0.455; P < 0.05) than pigs fed the DDGS or the DDGS-S diet, but no differences between the DDGS and the DDGS-S diets were observed. In a 10-d feed preference experiment (Exp. 3), 30 barrows (49.6 ± 2.3 kg of BW) were allotted to 3 treatment groups, with 10 replicates per group. The experimental procedures were the same as in Exp. 1, except that 30% DDGS was included in the DDGS and DDGS-S diets and 1.10% CaSO(4) was added to the DDGS-S diet. Feed preference for the DDGS and the DDGS-S diets, compared with the control diet, was 29.8 and 32.9%, respectively (P < 0.01), but there was no difference between the DDGS and the DDGS-S diets. In Exp. 4, a total of 120 barrows (34.2 ± 2.3 kg of BW) were fed grower diets for 42 d and finisher diets for 42 d. Diets were formulated as in Exp. 3. Pigs on the control diets gained more BW (1,021 vs. 912 and 907 g/d; P < 0.05) and had greater G:F (0.335 vs. 0.316 and 0.307; P < 0.05) than pigs fed the DDGS or DDGS-S diet, respectively, but no differences between pigs fed the DDGS and the DDGS-S diets were observed. In conclusion, dietary S concentration does not negatively affect feed preference, feed intake, or growth performance of weanling or growing-finishing pigs fed diets based on corn, soybean meal, and DDGS.     

Effects of dietary fat on growth performance and carcass characteristics of growing-finishing pigs reared in a commercial environment.

We conducted two experiments to evaluate the effects of added choice white grease on performance and carcass merit of barrows and gilts reared under commercial conditions. Pigs were housed either 20 (Exp. 1) or 25 (Exp. 2) per pen and were provided 0.67 m2 of pen space per pig. Diets were based on corn and soybean meal and fed in a meal form. The proportion of soybean meal was increased in diets with added fat to maintain the same calorie:lysine ratio in all diets within a weight phase. In Exp. 1, 480 pigs were fed diets with 0, 2, 4, or 6% fat. Total lysine contents of the control diets were 1.21, 0.88, and 0.66% during the weight phases 36 to 59, 59 to 93, and 93 to 120 kg, respectively. Gain:feed was increased linearly (P < 0.01) due to fat addition in all weight intervals and over the total experiment. The effect of added fat on ADG was not consistent among the weight phases; a linear (P < 0.01) improvement was found from 36 to 59 kg, but no effect was found during the heavier weight phases. Over the total experiment, however, ADG was improved (P < 0.01) linearly. Carcass traits were not affected by treatment. Experiment 2 used 900 pigs to evaluate possible carryover effects on performance and carcass merit from feeding 6% fat. The experiment was divided into four phases: 25 to 45, 45 to 70, 70 to 90, and 90 to 115 kg; lysine contents of the control diets fed in each phase were 1.23, 1.05, 0.81, and 0.63%, respectively. The six treatments consisted of no added fat throughout the experiment or 6% added fat fed from 25 to 45 kg, 25 to 70 kg, 25 to 90 kg, 25 to 115 kg, or 45 to 70 and 90 to 115 kg. Carryover effects for ADG and G:F (P < 0.07) were found for the 90- to 115-kg interval and for ADFI and ME intake (P < 0.05) for the 45- to 70- and 70-to 90-kg intervals. When fat was added in the previous weight interval, ADG and G:F were improved and ADFI and ME intake were decreased in the subsequent weight interval. Pigs fed fat from 25 to 115 kg had more (P < 0.05) backfat and lower (P < 0.05) carcass leanness than pigs on the other treatments. These data suggest that fat can be added or removed from diets of growing-finishing pigs without any detrimental carryover effects. In fact, the positive carryover effect on ADG and G:F from 95 to 115 kg suggests that feeding fat from 25 to 95 kg will maximize performance over the total growing-finishing period but minimize any detrimental effects of added fat on carcass leanness.     

Escherichia coli phytase improves growth performance of starter, grower, and finisher pigs fed phosphorus-deficient diets

Corn-soybean meal-based diets, consisting of a high-P control (HPC) containing supplemental dicalcium phosphate (DCP), a basal diet containing no DCP, and the basal diet plus Escherichia coli phytase at 500 or 1,000 phytase units per kilogram (FTU/kg; as-fed basis) were fed to evaluate growth performance in starter, grower, and finisher pigs. Pigs were blocked by weight and gender, such that average weight across treatments was similar, with equal numbers of barrows and gilts receiving each treatment in each block. In Exp. 1, 48 pigs with an average initial BW of 11 kg, housed individually, with 12 pens per diet, were used to evaluate growth performance over 3 wk. Overall ADG and G:F were increased linearly (P < 0.05) by dietary phytase addition. Final BW and plasma P concentrations at 3 wk also increased linearly (P < 0.05). In Exp. 2, 128 pigs with an average initial BW of 23 kg, housed four pigs per pen, with eight pens per diet, were used to evaluate growth performance over 6 wk. A linear increase in response to phytase was noted for ADG and G:F in all three 2-wk periods, as well as overall (P < 0.05). Percentage of bone ash also showed a linear increase (P < 0.01). In Exp. 3, 160 pigs (53 kg), housed five pigs per pen, with eight pens per diet, were used to evaluate growth performance over 6 wk. A linear increase was detected for final BW, as well as ADG and G:F in the first and second 2-wk periods, and overall (P < 0.01). Twenty-four 15-kg individually housed pigs were used to evaluate total-tract nutrient digestibility in Exp. 4. Daily absorption of P linearly increased (P < 0.05) with phytase supplementation. Results of this research indicate that E. coli phytase is effective in liberating phytate P for uptake and utilization by starter, grower, and finisher pigs.     

Effects of dried distillers grains with solubles on growing and finishing pig performance in a commercial environment

Three experiments were conducted to determine the optimal level of dried distiller grains with solubles (DDGS) from a common ethanol manufacturing facility and to determine the potential interactions between dietary DDGS and added fat on performance and carcass characteristics of growing and finishing pigs. All experiments were conducted at the same commercial facility and used DDGS from the same ethanol manufacturing facility. In Exp. 1, a total of 1,050 pigs (average initial BW 47.6 kg), with 24 to 26 pigs per pen and 7 pens per treatment, were fed diets containing 0 or 15% DDGS and 0, 3, or 6% added choice white grease in a 2 x 3 factorial arrangement in a 28-d growth study. Overall, there were no DDGS x added fat interactions (P >/= 0.14). There was an improvement (linear, P < 0.01) in ADG and G:F as the percentage of added fat increased. There was no difference (P = 0.74) in growth performance between pigs fed 0 or 15% DDGS. In Exp. 2, a total of 1,038 pigs (average initial BW 46.3 kg), with 24 to 26 pigs per pen and 10 pens per treatment, were fed diets containing 0, 10, 20, or 30% DDGS in a 56-d growth study. Pigs fed diets containing DDGS had a tendency for decreased ADG and ADFI (both linear, P = 0.09 and 0.05, respectively), but the greatest reduction seemed to occur between pigs fed 10 and 20% DDGS. In Exp. 3, a total of 1,112 pigs (average initial BW 49.7 kg), with 25 to 28 pigs per pen and 9 pens per treatment, were used in a 78-d growth study to evaluate the effects of increasing DDGS (0, 5, 10, 15, or 20%) in the diet on pig growth performance and carcass characteristics. From d 0 to 78, ADG and ADFI decreased linearly (P 相似文献   

Efficacy of chromium picolinate on performance and tissue accretion in pigs with different lean gain potential.

We conducted two experiments to determine whether the efficacy of chromium picolinate (CrP) on growth performance, carcass composition, and tissue accretion rates is dependent on the lean gain potential of the pigs. In Exp. 1, 40 barrows (20 from each of two genetic backgrounds; two pigs per pen, five pens per treatment) were fed a fortified, corn-soybean meal basal diet (.95% lysine from 19 to 55 kg BW; .80% lysine from 55 to 109 kg BW) without or with 200 microg/kg of Cr from CrP. The addition of Cr had no effect on performance, carcass measurements, or accretion rates of carcass protein or lipid, regardless of the lean gain potential of the pigs. In Exp. 2, 60 group-penned pigs (three pigs per pen; five pens per treatment) were fed a fortified, corn-soybean meal basal diet without or with 200 microg/kg of Cr from CrP from 21 to 104 kg BW. Within the dietary Cr treatments, half of the pigs received daily injections of 3 mg of porcine somatotropin (pST) from 54 to 104 kg BW. The pST administration resulted in faster growth rates (P < .007), improved feed efficiency (P < .001), increased longissimus area (P < .001), and decreased 10th-rib backfat (P < .001). Administration of pST also increased the percentage and accretion rate of carcass protein (P < .001) and decreased the percentage and accretion rate of carcass lipid (P < .001). The addition of CrP to the diet had no effect on any variable measured in either the untreated or pST-treated pigs. In these studies, Cr was ineffective at altering the composition of the carcass and its effects were not dependent on the pig's potential for lean gain.     

Impact of betaine on pig finishing performance and carcass composition

Two experiments were conducted to evaluate the effect of betaine supplementation of finishing diets on growth performance and carcass characteristics of swine. Experiment 1 included 288 pigs in a 2 x 2 x 3 factorial arrangement of treatments consisting of barrows and gilts of two genetic populations fed diets with 1.25 g/kg supplemental betaine from either 83 or 104 kg to 116 kg and control pigs fed betaine-devoid diets. Pigs were housed three pigs per pen with eight replicate pens per treatment. Diets were corn-soybean meal-based with 300 ppm added choline. Genetic populations differed (P < 0.05) in fat depth (2.24 vs 2.93 cm) and longissimus muscle depth (53.8 vs 49.1 mm) at 116 kg. Betaine reduced feed intake (P < 0.05); however, real-time ultrasound measurements were not affected. In Exp. 2, 400 pigs were used in a 2 x 2 x 2 factorial arrangement of treatments to evaluate the effect of sex (barrow or gilts), betaine (0 or 1 g/kg of diet), and crude protein (CP) (0.70% lysine = 12.7% CP or 0.85% lysine = 15.0% CP) when fed from 60 to 110 kg live weight. Pigs had been assigned to either a high- or low-protein feeding regimen at an average initial weight of 11.3 kg and were maintained on their respective protein levels throughout the experiment. For a 56-d period from 61.7 kg to 113.6 kg, pigs were fed diets with 300 ppm added choline. Within each protein level, pigs were randomly assigned to diets containing 0 or 1 g/kg betaine. Pigs were group-housed (four to five pigs per pen). Pig weight and feed intake were recorded every 28 d. Real-time ultrasound measurements were recorded initially and at d 28 on 64 pigs, and on all pigs prior to slaughter. Growth rate was fastest and feed intake greatest for barrows (P < 0.05) and for pigs receiving 12.7% crude protein. A crude protein x betaine interaction (P < 0.05) was observed from d 28 to 56 with pigs fed the 15% CP diet growing fastest when supplemented with 1 g/kg betaine, and pigs receiving the 12.7% CP diet growing fastest when the diets contained 0 g/kg betaine. Gilts more efficiently (P < 0.05) converted feed into body weight gain, as did pigs receiving the 12.7% CP diet (P < 0.05). Longissimus muscle area and fat measurements were unaffected by betaine or dietary protein on d 28. However, by d 56 betaine reduced average fat depth in barrows (P < 0.05; 3.21 vs 3.40 cm), but not in gilts. Betaine may be more effective at altering body composition in barrows than in gilts.     

Additivity of effects from dietary copper and zinc on growth performance and fecal microbiota of pigs after weaning

Four experiments were conducted to determine the interactive effects of pharmacological amounts of Zn from ZnO and Cu from organic (Cu-AA complex; Cu-AA) or inorganic (CuSO(4)) sources on growth performance of weanling pigs. The Cu was fed for 4 (Exp. 1) or 6 (Exp. 2, 3, and 4) wk after weaning, and Zn was fed for 4 (Exp. 1) or 2 (Exp. 2, 3, and 4) wk after weaning. Treatments were replicated with 7 pens of 5 or 6 pigs per pen (19.0 ± 1.4 d of age and 5.8 ± 0.4 kg of BW, Exp. 1), 12 pens of 21 pigs per pen (about 21 d of age and 5.3 kg of BW, Exp. 2), 5 pens of 4 pigs per pen (20.3 ± 0.5 d of age and 7.0 ± 0.5 kg of BW, Exp. 3), and 16 pens of 21 pigs per pen (about 21 d of age and 5.7 kg of BW, Exp. 4). In Exp. 1 and 2, Cu-AA (0 vs. 100 mg/kg of Cu) and ZnO (0 vs. 3,000 mg/kg of Zn) were used in a 2 × 2 factorial arrangement. Only Exp. 1 used in-feed antibiotic (165 mg of oxytetracycline and 116 mg of neomycin per kilogram feed), and Exp. 2 was conducted at a commercial farm. In Exp. 3, sources of Cu (none; CuSO(4) at 250 mg/kg of Cu; and Cu-AA at 100 mg/kg of Cu) and ZnO (0 vs. 3,000 mg/kg of Zn) were used in a 3 × 2 factorial arrangement. In Exp. 4, treatments were no additional Cu, CuSO(4) at 315 mg/kg of Cu, or Cu-AA at 100 mg/kg of Cu to a diet supplemented with 3,000 mg/kg of Zn from ZnO and in-feed antibiotic (55 mg of carbadox per kilogram of feed). In Exp. 1 and 2, both Zn and Cu-AA improved (P < 0.001 to P = 0.03) ADG and ADFI. No interactions were observed, except in wk 1 of Exp. 2, where Zn increased the G:F only in the absence of Cu-AA (Cu-AA × Zn, P = 0.04). A naturally occurring colibacillosis diarrhea outbreak occurred during this experiment. The ZnO addition reduced (P < 0.001) the number of pigs removed and pig-days on antibiotic therapy. In Exp 3, ADFI in wk 2 was improved by Zn and Cu (P < 0.001 and P = 0.09, respectively) with no interactions. In wk 1, G:F was reduced by ZnO only in the absence of Cu (Cu × Zn, P = 0.03). Feeding Zn decreased fecal microbiota diversity in the presence of CuSO(4) but increased it in the presence of Cu-AA (Cu source × Zn, P = 0.06). In Exp. 4, Cu supplementation improved the overall ADG (P = 0.002) and G:F (P < 0.001). The CuSO(4) effect on G:F was greater (P < 0.001) than the Cu-AA effect. Our results indicate that pharmacological amounts of ZnO and Cu (Cu-AA or CuSO(4)) are additive in promoting growth of pigs after weaning.     

Growing-finishing performance and carcass characteristics of pigs fed normal and genetically modified low-phytate corn

A genetically modified corn hybrid homozygous for the lpa1 allele, containing low phytate (LP), and its nearly isogenic equivalent hybrid (normal) were compared in two experiments with growing-finishing swine. In Exp. 1, 210 barrows (27 kg) were allotted to one of six dietary treatments with two corn hybrids (LP and normal) and three P feeding regimens. There were five replicate pens (seven pigs/pen) per treatment. Treatments consisted of diets that were supplemented with P throughout the growing-finishing period (.2% P and .15% supplemental P during growing and finishing phases, respectively) or only during the growing phase (.2% supplemental P) or that were not supplemented with P throughout the growing-finishing period. Performance at the end of the growing phase was based on a 2 x 2 factorial arrangement of treatments with two corn hybrids and two levels of added P (0 and .2%). This resulted in 10 replicates for the treatments supplemented with .2% P. The finishing phase (73 to 112 kg) was a 2 x 3 factorial arrangement of treatments with the two types of corn and three regimens of added P during the finishing period. Breaking load (BL) and ash of the fourth metacarpal were evaluated from one pig/pen at the end of the growing phase and from all pigs after slaughter. Pigs fed the LP corn diet without added P had greater body weight gain, feed efficiency, BL, and ash content of the fourth metacarpal than pigs fed the normal corn diet without added P. Performance was similar between pigs fed the LP diet without added P and pigs fed LP and normal corn with added P. In Exp. 2, 1,092 gilts (34 kg body weight) were allotted by weight in a commercial facility to one of three treatments: 1) normal corn/soybean meal diet containing .29% and .22% available P during the growing and finishing phases, respectively; 2) LP corn/soybean meal diet with the same available P level as Treatment 1; and 3) same as Treatment 2 for 8 wk, then no inorganic P supplementation during the finishing phase. All pigs were slaughtered at approximately 122 kg. There were no significant differences in growing-finishing performance or BL among treatments. However, pigs fed diets containing LP corn possessed carcasses with less backfat and a higher percentage of lean (P < .01). These results confirm that the P in LP corn is available to the pig and suggest that pigs fed diets containing this genetically modified corn will have more desirable carcasses.     

Effects of dietary humic substances on pig growth performance, carcass characteristics, and ammonia emission

Five experiments were conducted to test the effects of various dietary humic substances (HS; HS1, 2, 3, and 4, each with different fulvic and humic acid contents) on pig growth, carcass characteristics, and ammonia emission from manure. In Exp. 1, 120 pigs were allotted to 3 dietary treatments without HS (control) or with HS1 at 0.5 and 1.0% (8 pens/treatment and 5 pigs/pen) and fed diets, based on a 5-phase feeding program, from weaning (d 21.3 +/- 0.3 of age) to 60 kg of BW. In Exp. 2 and 3, 384 pigs (192 for each experiment) were allotted to 3 dietary treatments without HS, with HS1, or with HS2 (0.5%) for Exp. 2 and without HS, or with HS3 or HS4 (0.5%) for Exp. 3 (8 pens/treatment and 8 pigs/pen in each experiment). Pigs were fed diets, based on a 6-phase feeding program, from weaning (25.4 +/-0.2 and 23.6 +/-0.3 d of age for Exp. 2 and 3, respectively) to 110 kg of BW. In Exp. 4, 96 pigs were weaned at 22.1 +/-0.2 d of age and allotted to 2 treatments without or with HS1 at 0.5% (6 pens/treatment and 8 pigs/pen), and in Exp. 5 96 pigs were weaned at 20.9 +/-0.3 d of age and allotted to 3 treatments without HS, or with HS3 or HS4 (0.5%; 4 pens/treatment and 8 pigs/pen). Pigs were fed the diets for at least 2 wk before they were moved to an environmental chamber to measure aerial ammonia and hydrogen sulfide for 48 h at 5-min intervals. In Exp. 1, pigs fed diets with HS1 at 0.5% had greater (P < 0.05) ADG during phase 3 and greater (P < 0.05) G:F during phases 3 and 5 than control pigs. In Exp. 2, pigs fed diets with HS1 or HS2 at 0.5% had greater (P < 0.05) ADG and G:F than control pigs during the entire feeding period, whereas in Exp. 3 HS3 or HS4 did not improve pig growth performance. Ammonia emission from manure was reduced by 18 or 16% when pigs were fed diets with HS1 (P = 0.067) or HS4 (P = 0.054), respectively. The results of this study indicate that the effects of dietary HS are variable but may improve growth performance of pigs and reduce ammonia emission from manure. Further research is needed to clarify these effects and the mechanisms by which HS may cause them.     

Effects of restricted feed intake on finishing pigs weighing between 68 and 114 kilograms fed twice or 6 times daily

In a previous study with limit-fed gestating gilts, we observed that gilts fed 6 times/d had greater ADG than those fed the same amount over 2 feedings. To confirm these earlier responses, we used finishing pigs as a model in two 42-d trials and two 28-d trials to evaluate the effects of restricted feed intake and feeding frequency (2 vs. 6 times/d, floor fed) on pig performance between 68 and 114 kg. In all experiments, pigs (10/pen) were housed in 1.8 × 3.1 m pens with a half-solid, half-slatted concrete floor. Pigs were fed a corn- and soybean meal-based diet formulated to 1.15% standardized ileal digestible Lys and 3,294 kcal of ME/kg. In Exp. 1 to 3, energy and Lys were supplied to pigs according to NRC (1998) calculations to target an ADG of 0.80 kg. In Exp. 4, the diet was supplied to pigs to target an ADG of 0.80 kg (low feed intake) or 0.95 kg (high feed intake) to determine if the amount of energy above the maintenance requirement and feeding frequency affected pig performance. Pigs were fed by dropping similar amounts of feed onto the solid concrete floor either 2 (0700 or 1400 h) or 6 times (3 meals within 2 h at the morning and afternoon feedings) per day with an Accu-Drop Feed Dispenser (AP Systems, Assumption, IL). In Exp. 1 and 2, pigs fed 6 times daily had increased (P < 0.02) ADG and G:F compared with pigs fed 2 times per day. Greater feeding frequency increased (P < 0.05) the duration of time spent feeding and standing and reduced the lying time. In Exp. 3, a third treatment was included to determine whether the improvements in performance were due to decreased feed wastage. This treatment was designed to minimize feed wastage by dropping feed closer to the floor for pigs fed 2 times per day. Pigs fed 6 times daily had improved (P < 0.05) ADG and G:F compared with pigs in either treatment fed 2 times per day. No difference (P > 0.05) in performance was observed between pigs fed 2 times per day when feed was dropped from the feed drop or by the modified method. In Exp. 4, increasing the feeding frequency from 2 to 6 times per day improved (P < 0.01) ADG and G:F for pigs fed the low feed intake and tended to increase (P < 0.06) ADG and improved (P < 0.05) G:F for pigs fed the high feed intake. In limit-feeding situations, increasing the frequency of feeding from 2 to 6 times per day improved pig performance, which confirmed our earlier findings in gestating gilts.     

Effect of dietary L-carnitine on growth performance and body composition in nursery and growing-finishing pigs.

Two experiments were conducted to determine the effect of dietary L-carnitine on growth performance and carcass composition of nursery and growing-finishing pigs. In Exp. 1,216 weanling pigs (initially 4.9 kg and 19 to 23 d of age) were used in a 35-d growth trial. Pigs were blocked by weight in a randomized complete block design (six pigs per pen and six pens per treatment). Four barrows and four gilts were used to determine initial carcass composition. L-Carnitine replaced ground corn in the control diets to provide 250, 500, 750, 1,000, or 1,250 ppm. On d 35, three barrows and three gilts per treatment (one pig/block) were killed to provide carcass compositions. L-Carnitine had no effect (P > 0.10) on growth, percentages of carcass CP and lipid, or daily protein accretion. However, daily lipid accretion tended to decrease and then return to values similar to those for control pigs (quadratic P < 0.10) with increasing dietary L-carnitine. In Exp. 2, 96 crossbred pigs (initially 34.0 kg BW) were used to investigate the effect of increasing dietary L-carnitine in growing-finishing pigs. Pigs (48 barrows and 48 gilts) were blocked by weight and sex in a randomized complete block design (two pigs/pen and eight pens/treatment). Dietary L-carnitine replaced cornstarch in the control diet to provide 25, 50, 75, 100, and 125 ppm in grower (34 to 56.7 kg; 1.0% lysine) and finisher (56.7 to 103 kg; 0.80% lysine) diets. At 103 kg, one pig/pen was slaughtered, and standard carcass measurements were obtained. Dietary L-carnitine did not influence growth performance (P > 0.10). However, increasing dietary carnitine decreased average and tenth-rib back-fat (quadratic, P < 0.10 and 0.05), and increased percentage lean and daily CP accretion rate (quadratic, P < 0.05). Break point analysis projected the optimal dosage to be between 49 and 64 ppm of L-carnitine for these carcass traits. It is concluded that dietary carnitine fed during the nursery or growing-finishing phase had no effect on growth performance; however, feeding 49 to 64 ppm of L-carnitine during the growing-finishing phase increased CP accretion and decreased tenth-rib backfat.     

Evaluating processing temperature and feeding value of extruded-expelled soybean meal on nursery and finishing pig growth performance

We conducted two experiments comparing the use of extruded-expelled soybean meal (EESoy) to solvent-extracted soybean meal (SBM) in swine diets. In Exp. 1, the objective was to determine the optimal processing temperature of EESoy for nursery pig growth performance. Pigs (n = 330, 13.2 +/- 2.3 kg of BW) were fed a control diet containing SBM with added fat or one of five diets containing EESoy extruded at 143.3, 148.9, 154.4, 160.0, or 165.6 degrees C. All diets were formulated on an equal apparent digestible lysine:ME ratio. From d 0 to 20, no differences were observed (P > 0.32) in ADG or ADFI (average of 544 and 924 g/d, respectively). However, gain:feed ratio (G/F) improved (quadratic, P < 0.01, range of 0.56 to 0.60) with increasing processing temperature, with the greatest improvement at 148.9 degrees C. In Exp. 2, the objective was to determine the feeding value of EESoy relative to SBM with or without added fat for growing-finishing pigs in a commercial production facility. A total of 1,200 gilts (initially 24.5 +/- 5.1 kg of BW) was used, with 25 pigs per pen and eight replications per treatment. Dietary treatments were arranged in a 2 x 3 factorial, with two sources of soybean meal (SBM or EESoy) and three levels of added fat. Pigs were phase-fed four diets over the experimental period and added fat (choice white grease) levels were 0, 3.4, and 7% initially, with the added fat levels decreasing in the next three dietary phases. Energy levels were based such that the higher energy in EESoy (with or without added fat) was calculated to be equal to that provided by SBM with added fat. From 24.5 to 61.2 kg, pigs fed EESoy had greater (P < 0.07) G/F than those fed SBM. Increasing added fat in either EESoy- or SBM-based diets increased G/F (linear, P < 0.0003). From 61.2 to 122.5 kg, ADG and G/F were unaffected in pigs fed EESoy and/or increasing added fat (P > 0.10). For the overall growing-finishing period, ADG was unaffected (P > 0.61) by increasing energy density of the diet; however, ADFI decreased (P < 0.05) and G/F increased (P < 0.02, range of 0.37 to 0.40) as energy density increased with either EESoy or added fat. Carcass leanness was not affected by dietary treatment. These results indicate that EESoy should be extruded at 148.9 to 154.4 degrees C, and that increasing dietary energy density by using EESoy and/or added fat improves feed efficiency in finishing pigs reared in a commercial environment.     

Effects of lysine:calorie ratio on growth performance of 10- to 25-kilogram pigs

Crossbred barrows (n = 336 Newsham Hybrids) initially 9.9 kg and 31+/-2 d of age were used to evaluate the effects of energy density and lysine:calorie ratio on growth performance. Pigs were allotted by initial weight in a 3 x 4 factorial arrangement of treatments in a randomized complete block design with six replicate pens per treatment. Each pen had four or five pigs with an equal number of pigs per pen within replicate. Pigs were fed increasing dietary energy densities (3.25, 3.38, and 3.51 Mcal ME/kg) and lysine:calorie ratios (3.00, 3.45, 3.90, and 4.35 g lysine/Mcal ME). Energy density was changed by levels of choice white grease (0, 3, and 6%), and lysine:calorie ratio was changed by altering the corn:soybean meal ratio. Over the 21-d trial, an energy density x lysine:calorie ratio interaction was observed for ADG (P < .05). Pigs fed diets containing 3.25 or 3.51 Mcal ME/kg had increasing ADG with increasing lysine:calorie ratio, whereas ADG of pigs fed 3.38 Mcal ME/kg was not affected by lysine:calorie ratio. Feed efficiency (gain:feed ratio) increased and ADFI decreased as lysine:calorie ratio increased (linear, P < .01) and as energy density increased (quadratic, P < .01 and .10, respectively). On d 21, two pigs per pen were scanned ultrasonically for backfat depth. An energy density x lysine:calorie ratio interaction (P < .06) was observed. Pigs fed diets containing 3.25 and 3.38 Mcal ME/kg had decreasing fat depth as lysine:calorie ratio increased; however, backfat depth was not affected by lysine:calorie ratio and was greatest for pigs fed 3.51 Mcal ME/kg. These results suggest that 10- to 25-kg pigs fed diets containing 3.38 Mcal ME/kg had maximum feed efficiency and that they required at least 4.35 g lysine/Mcal ME. However, pigs fed 3.51 Mcal ME/kg had increased fat depth regardless of calorie:lysine ratio.     

Rice mill feed as a replacement for broiler litter in diets for growing beef cattle

The efficacy of replacing broiler litter with rice mill feed was evaluated in four experiments. In Exp. 1, 40 predominantly Angus steers (initial BW = 277+/-18.2 kg) were fed four dietary treatments for 112 d (five steers per pen; two pens per diet). Dietary treatments (DM basis) were as follows: 1) 47% broiler litter:53% corn; 2) 60% rice mill feed:40% corn; 3) 50% rice mill feed:50% corn; and 4) 40% rice mill feed:60% corn. All diets, along with bermudagrass hay, were fed free choice. Daily gains were faster (P < 0.10) for the 50:50 and 40:60 diets (1.26 and 1.30 kg/d, respectively) than for the broiler litter diet (0.89 kg/d). Daily DMI was less (P < 0.10) by steers consuming rice mill feed-based diets than by those consuming broiler litter-based diets. In Exp. 2, 16 Angus x Charolais steers (initial BW = 277+/-22.7 kg) were fed the same four diets used in Exp. 1 while housed in individual metabolism stalls for determination of nutrient digestibility. Daily DMI was not different (P > 0.10) among diets. Nutrient digestibilities did not differ among diets (P > 0.10). In Exp. 3, 40 Continental cross steers (initial BW = 257+/-21.3 kg) were fed one of four dietary treatments for 112 d (five steers per pen; two pens per diet). On a DM basis, diets were as follows: 1) 47% broiler litter:53% soyhulls; 2) 70% rice mill feed:30% soyhulls; 3) 60% rice mill feed:40% soyhulls; and 4) 50% rice mill feed:50% soyhulls. All diets, along with bermudagrass hay, were fed free choice. Daily gains were less (P < 0.05) for the broiler litter diet than for the 60:40 and 50:50 diets (1.05, 1.16, and 1.28 kg/d, respectively), and steers fed the broiler litter diet consumed less DM than did steers fed the varying rice mill feed-based diets (P < 0.10). In Exp. 4, 16 Angus x Charolais steers (initial BW = 292+/-21.1 kg) were fed the same four diets as in Exp. 3 while housed in individual metabolism stalls for determination of nutrient digestibility. Daily DMI was less (P < 0.01) for the broiler litter diet (5.0 kg/d) than for the 70:30, 60:40, and 50:50 diets (7.8, 7.9, and 7.9 kg/ d, respectively). Digestibilities for DM, OM, and ADF did not differ (P > 0.10) among treatments; however, CP digestibility was greatest (P < 0.10) for the 60:40 diet, and NDF digestibility was least (P < 0.10) for the 70:30 diet. Rice mill feed can be used to replace broiler litter to formulate low-cost diets for stocker calves. Soyhulls and corn can be blended with rice mill feed to produce acceptable backgrounding diets for growing beef calves.     

Effect of microbial phytase on energy availability,and lipid and protein deposition in growing swine

Two experiments were conducted to determine the effect of phytase on energy availability in pigs. In Exp. 1, barrows (initial and final BW of 26 and 52 kg) were allotted to four treatments in a 2 x 2 factorial arrangement. Corn-soybean meal (C-SBM) diets were fed at two energy levels (2.9 and 3.2 x maintenance [M]) with and without the addition of 500 phytase units/kg of diet. The diets contained 115% of the requirement for Ca, available P (aP), and total lysine, and Ca and aP were decreased by 0.10% in diets with added phytase. Pigs were penned individually and fed daily at 0600 and 1700, and water was available constantly. Eight pigs were killed and ground to determine initial body composition. At the end of Exp. 1, all 48 pigs were killed for determination of carcass traits and protein and fat content by total-body electrical conductivity (TOBEC) analysis. Six pigs per treatment were ground for chemical composition. In Exp. 2, 64 barrows and gilts (initial and final BW of 23 and 47 kg) were allotted to two treatments (C-SBM with 10% defatted rice bran or that diet with reduced Ca and aP and 500 phytase units/kg of diet), with five replicate pens of barrows and three replicate pens of gilts (four pigs per pen). In Exp. 1, ADG was increased (P < 0.01) in pigs fed at 3.2 x M. Based on chemical analyses, fat deposition, kilograms of fat, retained energy (RE) in the carcass and in the carcass + viscera, fat deposition in the organs, and kilograms of protein in the carcass were increased (P < 0.10) in pigs fed the diets at 3.2 vs. 2.9 x M. Based on TOBEC analysis, fat deposition, percentage of fat increase, and RE were increased (P < 0.09) in pigs fed at 3.2 x M. Plasma urea N concentrations were increased in pigs fed at 3.2 x M with no added phytase but were not affected when phytase was added to the diet (phytase x energy, P < 0.06). Fasting plasma glucose measured on d 28, ultrasound longissimus muscle area (LMA), and 10th-rib fat depth were increased (P < 0.08) in pigs fed phytase, but many other response variables were numerically affected by phytase addition. In Exp. 2, phytase had no effect (P > 0.10) on ADG, ADFI, gain:feed, LMA, or 10th-rib fat depth. These results suggest that phytase had small, mostly nonsignificant effects on energy availability in diets for growing pigs; however, given that phytase increased most of the response variables measured, further research on its possible effects on energy availability seems warranted.     

Interaction of swine nursery and grow-finish space allocations on performance

Two experiments were conducted to evaluate the possible interaction of nursery space allocations and grow-finish space allocations in swine. In Exp. 1, crowding was achieved by varying the number of pigs per pen. During the nursery phase, decreasing the space allocation (0.16 m2/pig vs 0.25 m2/pig; 8 and 12 pens per treatment, respectively) by increasing the number of pigs per pen (18 vs 12) resulted in a decrease in daily feed intake (0.609 vs 0.683 kg/d; P < 0.001) and daily gain (0.364 vs 0.408 kg/d; P < 0.001). Pigs were mixed within nursery treatment groups and reassigned to grow-finish pens (6 pens per treatment) at the end of the 35-d nursery period providing either 0.56 m2/pig (14 pigs/pen) or 0.78 m2/pig (10 pigs/pen). Crowding during the grow-finish phase decreased daily feed intake (P < 0.003) and daily gain (P < 0.001). In Exp. 2, space allocations of 0.16 m2/pig vs 0.23 m2/pig during the nursery phase (24 pens per treatment) resulted in a decrease in daily feed intake (0.612 vs 0.654 kg/d; P < 0.005) and daily gain (0.403 vs 0.430 kg/d; P < 0.001). Pigs remained in the same (social) groups when moved to the grow-finish phase. Unlike Exp. 1, there was no effect of crowding during the grow-finish phase (0.60 m2/pig vs 0. 74 m2/pig) on daily feed intake or daily gain. The difference in results between experiments suggests that the response to crowding during the grow-finish phase may depend in part on whether pigs are mixed and sorted following movement from the nursery.     

Effects of source and level of copper on performance and liver copper stores in weanling pigs

Five 28- to 33-d experiments involving 460 crossbred pigs weaned at 28 +/- 2 d of age (initial weight, 6.7 to 8.1 kg) were conducted to determine the effects of feeding high dietary levels of Cu sulfate (CuSO4) or Cu oxide (CuO) on rate and efficiency of gain and liver Cu stores of weanling pigs. The pigs were housed in groups of five to six/pen and fed a fortified, unmedicated, corn-soybean meal-dried whey basal diet (1.1% lysine, 30 ppm Cu). In Exp. 1 and 2, pigs (eight replicates) were fed the basal or the basal plus 125 or 250 ppm Cu from CuSO4 or CuO for 28 d. In Exp. 3 and 4, four replications were fed the same diets as in Exp. 1 and 2 plus two additional diets (500 ppm Cu from CuSO4 or CuO). In Exp. 5, dietary levels of 0, 125, 250, 375 or 500 ppm Cu from CuSO4 were evaluated using four replications. At the end of each experiment, the liver from one pig in each pen was collected for Cu analysis. Overall, rate and efficiency of gain were improved (P less than .01) by feeding 125 or 250 ppm Cu as CuSO4, with the 125 ppm dietary level being about 75% as effective in stimulating growth as 250 ppm. Performance of pigs was not different from controls when the highest (500 ppm) level of Cu (from CuSO4) was fed. Liver Cu increased 10- to 70-fold when 250 to 550 ppm Cu from CuSO4 was included in the feed.(ABSTRACT TRUNCATED AT 250 WORDS)     

The effects of dietary energy concentration and weaning site on weanling pig performance

This study was conducted to evaluate the effects of dietary energy density and weaning environment on pig performance. Treatment diets were formulated to vary in DE concentration by changing the relative proportions of low (barley) and high (wheat, oat groats, and canola oil) energy ingredients. In Exp. 1, 84 pigs in each of 3 replications, providing a total of 252 pigs, were weaned at 17 x 2 d of age and randomly assigned to either an on-site or an off-site nursery and to 1 of 3 dietary DE concentrations (3.35, 3.50, or 3.65 Mcal/kg). Each site consisted of a nursery containing 6 pens; 3 pens housed 7 barrows and 3 housed 7 gilts. All pigs received nontreatment diets in phase I (17 to 19 d of age) and phase II (20 to 25 d of age), respectively. Dietary treatments were fed from 25 to 56 d of age. Off-site pigs were heavier at 56 d of age (23.4 vs. 21.3 kg; P < 0.05) and had greater ADFI (0.77 vs. 0.69 kg/d; P < 0.01) than on-site pigs. There was a linear decrease in ADG (P < 0.01) and ADFI (P < 0.001) with increasing DE concentration. Efficiency of gain improved (P < 0.01) with increasing DE concentration. There was no interaction between weaning site and diet DE concentration, indicating that on-site and off-site pigs responded similarly to changes in diet DE concentration. In Exp. 2, nutrient digestibility of the treatment diets used in Exp. 1 was determined using 36 pigs with either ad libitum or feed intake restricted to 5.5% of BW. Energy and N digestibility increased (P < 0.001) with increasing DE concentration. Nitrogen retention and daily DE intake increased with DE concentration in pigs fed the restricted amount of feed (P < 0.05). These results indicate that weaning off-site improves pig weight gain. The weanling pig was able to compensate for reduced dietary DE concentration through increased feed intake. Growth limitation in the weanling pig may not be overcome simply by increasing dietary DE concentration.