Influence of dietary methionine concentration on growth and nitrogen balance in weanling Quarter Horses.

Twenty-four Quarter Horse weanlings (120 ± 10 d) were blocked by age into 4 groups (n=6) for a 56-d trial to evaluate the influence of dietary Met concentration on growth and N balance. Weanling horses were housed by block and individually fed concentrates twice daily at 1.75% BW (as-fed basis). Weanling horses were randomly assigned to 1 of 4 concentrate treatments: basal (0.20 Met), basal + 0.03% Met (0.23 Met), basal + 0.07% Met (0.27 Met), and basal + 0.11% Met (0.31 Met). Diets were formulated to be isonitrogenous and isocaloric and contained equal amounts of Lys and Thr. Coastal bermudagrass hay (Cynodon dactylon) was individually fed at 0.75% BW (as-fed basis). Growth measurements, BW, rump fat, and plasma were obtained every 7 d. The final 4 d consisted of total collection of urine and feces. Feed, fecal, and urine samples were analyzed for N content, and N balance was calculated. Urine was analyzed for urea and ammonia concentrations. Plasma was analyzed for urea concentration. Grain, hay, and fecal samples were analyzed for nutrient composition. Data were analyzed using the PROC MIXED procedure of SAS. Linear, quadratic, and cubic effects were tested in the form of contrasts. There was no influence (P>0.25) of treatment on growth measurements, N balance, or urinary urea or ammonia. Intake of Lys and Thr did not differ (P>0.08) among treatments. Methionine intake increased as expected with increasing Met inclusion in the diet (P<0.01). Plasma urea N responded quadratically (P=0.04) to treatment. An unexpected peak in PUN was observed with 0.27 Met. The results indicate future studies that can ensure Met as the only dietary variable are necessary to better explain the Met requirements of weanling horses.

Effects of direct-fed microbial supplementation on digestibility and fermentation end-products in horses fed low- and high-starch concentrates.

A study was conducted to determine whether direct-fed microbials (DFM) could be used to increase digestibility and minimize the risk of acidosis associated with feeding an increase in the amount of starch fed to horses. Fifteen mature Thoroughbred geldings were randomly assigned to 1 of 3 treatments in a 3 x 3 Latin square design balanced for carryover effects. Within each 26-d period, horses were offered grass hay + low-starch concentrate (LS; 1.2 g of starch x kg of BW(-1) x meal(-1)) from d 1 to 13 and then were abruptly changed to hay + high-starch concentrate (HS; 2.4 g of starch.kg of BW(-1)x meal(-1)) on d 14 continuing through d 26. The DFM treatments were offered in concentrate pellets at a target dosage of 10(8) cfu/(50 kg of BW x d) as follows: no DFM (CON; control), Lactobacillus acidophilus (LAC1; single-species DFM), or a mixture of L. acidophilus, Lactobacillus casei, Bifidobacterium bifidum, and Enterococcus faecium (LAC4; multiple-species DFM). Total feces were collected over 72 h from d 11 to 13 (LS; low dietary starch collection), from d 15 to 17 (AC; abrupt change in dietary starch collection), and at the end of each experimental period, from d 24 to 26 (HS; high dietary starch collection). Data collected consisted of total DM intake and fecal output, fecal pH, fecal acetate and propionate concentrations, and viable numbers of DFM in the feed. With the exception of Fe digestibility, there were no starch x DFM interactions. There was an effect of starch level (P 0.10). Horses supplemented with LAC4 had increased ether extract (P < 0.05) and a tendency for decreased Na (P < 0.10) digestibilities compared with CON horses. All DFM-supplemented horses had increased Cu (P < 0.05) and Fe and numerically increased Zn digestibilities compared with CON horses. Fecal pH decreased (P < 0.05), and fecal propionate concentration increased (P < 0.05) as dietary starch content changed from LS to HS. There was a tendency for elevated fecal pH (P < 0.10) in LAC1 horses compared with CON horses. These results confirm that increasing starch in the equine diet can enhance nutrient digestibility of the diet. Supplementing equine diets with either a single or mixed strain direct-fed lactic acid bacteria had limited effects on nutrient digestibility or on reducing the risk of acidosis associated with feeding high-starch concentrates to horses. The potential response of DFM supplementation should be evaluated when a more acute acidotic state is induced in horses than in the current study.

The effects of phytase on growth performance and intestinal transit time of broilers fed nutritionally adequate diets and diets deficient in calcium and phosphorus.

Five experiments (Exp.) were conducted to determine the effects of phytase on growth performance and intestinal transit time in chicks fed nutritionally adequate diets and diets deficient in Ca and nonphytate P (nPP). In Exp. 1 and 2, chicks were fed a nutritionally adequate diet from 0 to 6 d or from 0 to 4 d posthatching; assay periods were 8 or 10 d; average initial BW were 98 or 79 g; and average final BW were 371 or 369 g, respectively. Treatments were replicated with 12 pens of 5 chicks each. Corn-soybean meal (C-SBM) diets were adequate in all nutrients except Ca and nPP where appropriate. The treatments were 1) C-SBM, 1.0% Ca, and 0.45% nPP; 2) C-SBM, 0.80% Ca, and 0.25% nPP; 3) Diet 1 + 600 phytase units/kg of diet; 4) Diet 2 + 600 phytase units/kg of diet. Experiments 3, 4, and 5 were conducted to determine the effects of phytase on intestinal transit time in broilers. Broilers were fed the same nutritionally adequate diet from 0 to 18, 27, or 23 d posthatching, and the assay periods were 7 d. Treatments were replicated with 18 individually penned broilers. Average initial BW were 768, 1,108, or 838 g, and average final BW were 1,299, 1,704, or 1,392 g in Exp. 3 to 5, respectively. Transit time data were collected on d 1 and 7 of the Exp. Diets were 1) C-SBM, 0.9% Ca, and 0.35% nPP; 2) C-SBM, 0.80% Ca, and 0.25% nPP + 600 phytase units/kg of diet. Transit time was calculated as the difference between the time feed was first ingested and the time of first appearance of solid feces. In Exp. 1 and 2, the reduction in dietary Ca and nPP reduced (P < 0.01) average daily gain (ADG), average daily feed intake (ADFI), and gain:feed. Phytase addition increased (P < 0.02) ADG and ADFI in diets deficient in Ca and nPP and in the nutritionally adequate diets. In Exp. 2, the reduction in Ca and nPP reduced (P < 0.01) toe and tibia ash percentage, but phytase addition increased (P < 0.01) toe and tibia ash percentage. The increase in toe ash percentage was greater in chicks fed the Ca and nPP deficient diet than in chicks fed the nutritionally adequate diet (Ca and nPP x phytase, P < 0.01). In Exp. 3, 4, and 5, transit time on d 1 was faster (P < 0.03) in chicks fed phytase. On d 7, transit time tended to be faster in chicks fed phytase, but the effect was not significant (P = 0.15). These data indicate that phytase increases ADG and ADFI in diets deficient in Ca and nPP and in diets formulated to be adequate (or excess) in all nutrients for broiler chicks. The increase in ADG and ADFI in chicks fed the nutritionally adequate diet may be due to a faster transit time of feed through the digestive tract, resulting in a greater feed intake and gain.

Effect of protein and energy sources and bulk density of diets on growth performance of chicks.

Four completely randomized designed experiments (EXP) were conducted to determine the effect of energy, amino acid (AA) levels, and bulk density of diets on growth performance of chicks fed diets containing corn (C) or cornstarch:dextrose (CD) as energy sources and soybean meal (SBM) or soy protein isolate (SPI) as protein sources. The chicks were fed C-SBM diets 6 to 8 d posthatching before allotment to treatment, and the assay periods ranged from 7 to 14 d. Initial weights were 86, 93, 94, and 71 g in EXP 1 to 4, respectively. Treatments were replicated 6 to 8 times with 4, 5, or 6 chicks per replicate. In EXP 1, the treatments were 1) C-SBM (1.26% Lys and 3,200 kcal of ME/kg); 2) CD-SPI (1.26% Lys and 3,460 kcal of ME/kg); 3) CD-SPI (1.36% Lys and 3,460 kcal of ME/kg); and 4) CD-SPI (1.26% Lys and 3,200 kcal of ME/kg). The AA in all diets were increased in proportion to Lys. In EXP 2, chicks were fed C or CD as the energy source and SBM or SPI as the protein source in a 2 x 2 factorial arrangement. In EXP 3, the treatments were 1) C-SBM (1.26% Lys and 3,200 kcal of ME/kg); 2) CD-SPI (1.26% Lys and 3,200 kcal of ME/kg); 3) Diet 1 limit-fed to chicks consuming 90% of Diet 2; 4) Diet 2 limit-fed to chicks consuming 90% of Diet 2. In EXP 4, Diets 1 and 2 were the same as Diets 1 and 2 in EXP 3, but fed in mash or pelleted form. In all EXP, chicks with access ad libitum to diets with SPI had decreased (P < 0.02) average daily gain (ADG) and feed intake (ADFI) compared with those with access ad libitum to diets with SBM. In EXP 2, feeding C- or CD-dextrose as the energy source had no effect (P > 0.05) on ADG, ADFI, or gain:feed. In EXP 3, ADG was decreased in chicks fed the diets with SPI relative to those fed diets with SBM, but the decrease was much greater in chicks that had access ad libitum to feed (protein source x feed intake, P < 0.01) than in those limit-fed to the same feed intake. In EXP 4, ADG, ADFI, and gain:feed were decreased (P < 0.01) in chicks fed diets with SPI as the protein source. Pelleting increased (P < 0.01) ADG, ADFI, and gain:feed regardless of protein source, but the increase was much greater in chicks fed the diets with SPI (protein source x feed form, P < 0.01). Results from these EXP indicate that diets with SPI compared with SBM do not result in maximum growth performance in commercial broilers, and the problem may be due somewhat to nutrient deficiency but more to the physical form of the diet.

The interactive effects of Eimeria acervulina infection and phytase for broiler chicks.

An experiment was conducted to determine the interactive effects of Eimeria acervulina infection and phytase in male broiler chicks. Chicks were standardized from 0 to 4 d posthatching, and the assay period was 5 to 15 d. Treatments were replicated with 6 pens of 5 chicks each. The initial and final BW were 67 and 363 g. A corn-soybean meal diet formulated to provide 1.26% total Lys and 3,200 kcal of ME/kg was used, and it was adequate in all other nutrients except Ca and nonphytate P (NPP) when appropriate. The treatments were in a 2 x 2 x 2 factorial arrangement: adequate Ca and NPP (1.0% Ca and 0.45% NPP) or inadequate Ca and NPP (0.80% Ca and 0.25% NPP), 0 or 600 phytase units/kg of diet, and uninfected or infected with 400,000 E. acervulina oocysts on d 0, 3, and 6 of the experiment. Daily gain, average daily feed intake, and gain:feed (GF) were reduced (P < 0.01) by the coccidial infection and the reduction in Ca and NPP. Phytase addition increased (P < 0.02) average daily gain and average daily feed intake, regardless of the Ca and NPP contents of the diet or the presence of coccidiosis. The GF was increased by phytase but only in uninfected chicks (phytase x coccidiosis, P < 0.02). Toe and tibia ash percentages were decreased (P < 0.01) in chicks fed diets deficient in Ca and NPP, but tibia ash was decreased more by Ca and NPP in healthy chicks than in infected chicks (coccidiosis x Ca and NPP, P < 0.02). Phytase increased (P < 0.02) toe and tibia ash but only in diets deficient in Ca and NPP (phytase x Ca and NPP, P < 0.01). Phytase increased toe ash percentage of healthy chicks fed diets deficient in Ca and NPP, but it had less of an effect in infected chicks fed diets deficient in Ca and NPP (coccidiosis x Ca and NPP x phytase, P < 0.08). Also, phytase was less effective in increasing tibia ash percentage in coccidiosis-infected chicks than in uninfected chicks (phytase x coccidiosis, P < 0.02). These data indicate that phytase is effective in the presence of a coccidial infection, but based on GF and tibia ash percentage, it may not be as effective as in uninfected chicks. Also, phytase increased average daily gain and average daily feed intake in uninfected chicks fed diets formulated to be adequate (or in excess) in all nutrients for male broiler chicks.

The tryptophan requirement of growing and finishing barrows.

Five experiments were conducted to determine the true ileal digestible Trp (tidTrp) requirement of growing and finishing pigs fed diets (as-fed basis) containing 0.87% (Exp. 3), 0.70% (Exp. 4), 0.61% (Exp. 5), and 0.52% (Exp. 1 and 2) tidLys during the early-grower, late-grower, early-finisher, and late-finisher periods, respectively. Treatments were replicated with three or four replications, with three or four pigs per replicate pen. Treatment differences were considered significant at P = 0.10. Experiment 1 was conducted with 27 pigs (initial and final BW of 78.3 +/- 0.5 and 109.8 +/- 1.9 kg) to validate whether a corn-feather meal (FM) tidTrp-deficient (0.07%) diet, when supplemented with 0.07% crystalline l-Trp, would result in growth performance and carcass traits similar to a conventional corn-soybean meal (C-SBM) diet. Pigs fed the corn-FM diet without Trp supplementation had decreased growth performance and carcass traits, and increased plasma urea N (PUN) concentration. Supplementing the corn-FM diet with Trp resulted in greater ADG and G:F than pigs fed the positive control C-SBM diet. Pigs fed the corn-FM diet had similar carcass traits as pigs fed the C-SBM diet, but loin muscle area was decreased and fat thickness was increased. In Exp. 2, 60 pigs (initial and final BW of 74.6 +/- 0.50 and 104.5 +/- 1.64 kg) were used to estimate the tidTrp requirement of finishing pigs. The levels of tidTrp used in Exp. 2 were 0.06, 0.08, 0.10, 0.12, or 0.14% (as-fed basis). Response variables were growth performance, PUN concentrations, and carcass traits and quality. For Exp. 2, the average of the estimates calculated by broken-line regression was 0.104% tidTrp. In Exp. 3, 4, and 5, barrows (n = 60, 60, or 80, respectively) were allotted to five dietary treatments supplemented with crystalline l-Trp at increments of 0.02%. The basal diets contained 0.13, 0.09, and 0.07% tidTrp (as-fed basis) in Exp. 3, 4, and 5, and initial BW of the pigs in these experiments were 30.9 +/- 0.7, 51.3 +/- 1.1, and 69.4 +/- 3.0 kg, respectively. The response variable was PUN, and the basal diet used in Exp. 3 and 4 contained corn, SBM, and Canadian field peas. The tidTrp requirements were estimated to be 0.167% for pigs weighing 30.9 kg, 0.134% for pigs weighing 51.3 kg, and 0.096% for pigs weighing 69.4 kg. Based on our data and a summary of the cited literature, we suggest the following total Trp and tidTrp requirement estimates (as-fed basis): 30-kg pigs, 0.21 and 0.18%; 50-kg pigs, 0.17 and 0.14%; 70-kg pigs, 0.13 and 0.11%; and in 90-kg pigs, 0.13 and 0.11%.

Effect of microbial phytase addition with or without the trace mineral premix in nursery, growing, and finishing pig diets.

Two experiments were conducted to determine the interactive effects of phytase with and without a trace mineral premix (TMP) in diets for nursery, growing, and finishing pigs on growth performance, bone responses, and tissue mineral concentrations. Pigs (initial and final BW of 5.5 and 111.6 kg [Exp. 1] or 5.4 and 22.6 kg [Exp. 2]) were allotted to treatments on the basis of BW with eight (Exp. 1) or six (Exp. 2) replications of six or seven pigs per replicate pen. Pigs were started on the diets the day of weaning (average of 18 d). In both experiments, the treatments were with or without 500 phytase units/kg of diet and with or without the TMP in a 2 x 2 factorial arrangement. The Ca and available P concentrations were decreased by 0.10% in diets with phytase. The nursery phase consisted of Phase I (7 d), Phase II (14 d), and Phase III (13 d) periods. In Exp. 1, 26 of 52 pigs fed the diet without the TMP and without phytase had severe skin lesions and decreased growth performance; therefore, pigs fed this diet were switched to the positive control diet. In Exp. 2, the treatment without the TMP and without phytase had 12 replications instead of six. At the end of Phase III, half these replications were switched to the positive control diet and half were switched to the diet without the TMP but with phytase. In Exp. 1 during Phases II and III and in the overall data, pigs fed the diet without the TMP had decreased ADG and ADFI, but the addition of phytase prevented these responses (phytase x TMP; P < 0.02). Growth performance was not affected by diet during the growing-finishing period. Coccygeal bone Zn and Na concentrations were decreased (P < 0.09) in pigs fed the diet without the TMP, and adding phytase increased (P < 0.03) Zn and Fe concentrations. In Exp. 2 during Phases I and II, pigs fed the diet without the TMP had decreased ADG, but the addition of phytase prevented this response (phytase x TMP; P < 0.10). Pigs fed the diet without the TMP had decreased (P < 0.10) ADG (Phase II and overall), ADFI (Phases II and III and in the overall data), and G:F (Phase III). Coccygeal bone Zn and Cu concentrations were decreased (P < 0.09) in pigs fed the diet without the TMP, and adding phytase increased (P < 0.03) Zn concentration in the bones. These data indicate that removing the TMP in diets for nursery pigs decreases growth performance and bone mineral content, and that phytase addition to the diet without the TMP prevented the decreased growth performance.

Effects of microbial phytase, low calcium and phosphorus, and removing the dietary trace mineral premix on carcass traits, pork quality, plasma metabolites, and tissue mineral content in growing-finishing pigs.

An experiment was conducted to determine the effects of phytase addition, reduced Ca and available P (aP), and removing the trace mineral premix (TMP) on growth performance, plasma metabolites, carcass traits, pork quality, and tissue mineral content in growing-finishing swine. One hundred twenty cross-bred pigs (initial and final BW of 22 and 109 kg, respectively) were allotted to five dietary treatments on the basis of weight within gender in a randomized complete block design. There were three replications of barrows and three replications of gilts, with four pigs per replicate pen. The dietary treatments were as follows: 1) corn-soybean meal (C-SBM), 2) C-SBM with reduced Ca and aP, 3) C-SBM with reduced Ca and aP plus 500 phytase units/kg of diet, 4) Diet 1 without the TMP, and 5) Diet 3 without the TMP. The Ca and aP were reduced by 0.10% in the low Ca and aP diets and the diets with added phytase. Daily gain, hot carcass weight, dressing percent, kilograms of carcass lean, bone ash percent, and bone strength were decreased (P = 0.10), but liver and kidney weight were increased (P = 0.10) in pigs fed diets with reduced Ca and aP; adding phytase reversed these responses (P = 0.10). The Commission Internationale de I'Eclairage L* was decreased (P = 0.09) in pigs fed the low Ca and aP diet plus phytase relative to those fed the control diet. Removing the TMP had no effect on overall growth performance, but it increased (P = 0.03) 10th-rib backfat thickness and fasting glucose and decreased (P = 0.03) carcass length and ham weight. Liver weight and liver weight as a percentage of final BW were not affected when phytase was added to the control diet, but removing the TMP increased liver weight and liver weight as a percentage of final BW; adding phytase reversed these responses (phytase x TMP, P = 0.06). Removing the TMP decreased (P = 0.08) Zn concentrations in the bone, muscle, and liver, and Cu and Fe concentrations in the bile but increased (P = 0.08) Mn concentrations in the bile and liver of pigs. The addition of phytase reversed the negative effects of the reduced Ca and aP diets. These data indicate that removing the TMP in diets for growing-finishing pigs has no negative effects on growth performance or pork quality, but it had negative effects on carcass traits and had variable effects on tissue mineral content.

Effect of nonwaxy and waxy sorghum on growth, carcass traits, and glucose and insulin kinetics of growing-finishing barrows and gilts.

Two experiments were conducted to determine the effect of nonwaxy (amylose and amylopectin starch) or waxy (amylopectin starch) sorghum on growth, carcass traits, and glucose and insulin kinetics of pigs. In Exp. 1 (95-d), 60 crossbred barrows or gilts (initial and final BW of 24 and 104 kg) were allotted to three treatments with five replications of four pigs per replicate pen in a randomized complete block design. The dietary treatments for Exp. 1 were 1) corn-soybean meal (C-SBM) diet, 2) sorghum-SBM (red pericarp, non-waxy), and 3) sorghum-SBM (red pericarp, waxy). In Exp. 2, 28 crossbred barrows (initial and final BW of 24 and 64 kg) were allotted to two treatments with three replications of four or five pigs per replicate pen in a randomized complete block design. Growth data were collected for 49 d, and then 20 barrows were fitted with jugular catheters, and then a glucose tolerance test (500 mg glucose/kg BW), an insulin challenge test (0.1 IU of porcine insulin/kg BW), and a feeding challenge were conducted. The dietary treatments for Exp. 2 were 1) sorghum-SBM (white pericarp, nonwaxy) and 2) sorghum-SBM (white pericarp, waxy). In Exp. 1, ADG (P = 0.10) and ADFI (as-fed basis; P = 0.02) were increased (P = 0.10) and gain:feed was decreased (P = 0.04) in pigs fed the sorghum-SBM diets relative to those fed the C-SBM diet. These responses may have resulted from the lower energy content of sorghum relative to corn. Plasma NEFA concentration (collected after a 16-h fast on d 77) was decreased (P = 0.08) in pigs fed the waxy sorghum-SBM diet relative to those fed the nonwaxy sorghum-SBM diet. Kilograms of carcass fat was decreased (P = 0.07) in pigs fed the waxy sorghum-SBM diet relative to those fed the nonwaxy sorghum-SBM diet. In Exp. 2, there was no effect (P = 0.57 to 0.93) of sorghum starch type on growth performance by pigs. During the glucose tolerance and insulin challenge tests, there were no effects (P = 0.16 to 0.98) of diet on glucose or insulin kinetics. During the feeding challenge, glucose (P = 0.02) and plasma urea N (P = 0.06) area under the response curves from 0 to 90 min were decreased in pigs fed the waxy sorghum-SBM diet. Feeding waxy sorghum had minimal effects on growth and carcass traits relative to pigs fed corn or nonwaxy sorghum. Waxy sorghum vs. nonwaxy sorghum had no effect on glucose or insulin kinetics in pigs.

Effect of chromium propionate on growth, carcass traits, pork quality, and plasma metabolites in growing-finishing pigs.

Two experiments were conducted to determine the effects of dietary Cr, as Cr propionate, on growth, carcass traits, pork quality, and plasma metabolites in growing-finishing swine. Ninety-six crossbred gilts (Exp. 1; initial and final BW of 28 [SEM = 0.41] and 109 [SEM = 2.11] kg) or 144 PIC Cambrough 22 barrows (Exp. 2; initial and final BW of 26 [SEM = 0.39] and 111 [SEM = 2.52] kg) were allotted to six or four dietary treatments, respectively, with six replications and four (Exp. 1) or six (Exp. 2) pigs in each replicate pen blocked by weight in randomized complete block designs. The six dietary treatments for Exp. 1 were 1) corn-soybean meal (C-SBM), 2) C-SBM + 50 ppb Cr, 3) C-SBM + 100 ppb Cr, 4) C-SBM + 200 ppb Cr, 5) C-SBM low NE diet, and 6) C-SBM low NE diet + 200 ppb Cr. The four dietary treatments for Exp. 2 were C-SBM with 0, 100, 200, or 300 ppb Cr. Growth, carcass traits, and plasma metabolite (collected on d 29 and at each phase change) data were taken at the end of both experiments and pork quality data were taken at the end of Exp. 1. There was no effect (P > 0.10) on overall growth performance when pigs were fed graded levels of Cr (Exp. 1 and 2) or Cr in the positive control or low NE diets (Exp. 1). Longissimus muscle area, ham weight, ham fat-free lean, and total carcass lean were increased in pigs fed 200 ppb in the positive control diets but decreased in pigs fed 200 ppb Cr in the low NE diets (Cr x NE, P < 0.08). There was no effect of Cr concentration (P > 0.10) on carcass traits in Exp. 2. In Exp. 1, cook loss of a fresh or a frozen chop was decreased (P < 0.10) by 200 ppb Cr. In Exp. 1, NEFA concentration was decreased (P < 0.05) in pigs fed Cr in the positive control or low NE diets during the early-finishing period. In Exp. 2, the addition of Cr decreased NEFA (quadratic, P < 0.09) and plasma urea N (linear, P < 0.02) concentrations and tended to increase total cholesterol and high density lipoproteins (quadratic, P < 0.09). In these experiments, Cr propionate had no effect on overall growth performance, variable effects on carcass traits and plasma metabolites, and some positive effects on pork quality, especially water holding capacity of a fresh or frozen chop.

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.

Growth performance of different breed crosses of chicks fed diets with different protein and energy sources.

Six experiments (EXP) were conducted to evaluate growth performance of different breed crosses of broiler chicks fed diets containing soybean meal, soy protein isolate (SPI), soy protein concentrate (SPC), or rice and casein. Cornish x Plymouth Rock (C x PR; EXP 1, 3, 4, 5, and 6) or New Hampshire x Columbian (NH x C; EXP 2 and 4) cross chicks were used. The chicks were fed a corn-soybean meal (C-SBM) diet before allotment to treatment. The age of the chicks ranged from 5 to 9 d posthatching at the start of the EXP, and the assay periods ranged from 8 to 14 d. Initial weights were 194.9, 96.1, 102.1, 84.7 [84.1 (C x PR) or 85.3 (NH x C)], 101.8, and 145.1 g in EXP 1 to 6, respectively. A completely randomized design was used in all EXP, and treatments were replicated four to six times with four or five chicks each. All diets were formulated to meet the NRC nutrient requirements of chicks. In EXP 1 (C x PR male chicks) and EXP 2 (NH x C female chicks), gain and gain:feed (G:F) were greater (P < 0.01) in chicks fed the C-SBM diet compared with chicks fed diets containing SPI. In EXP 3, C x PR chicks were fed a C-SBM diet, a SPI-dextrose-cornstarch diet (dextrose:cornstarch, 1:1) formulated by Louisiana State University Agricultural Center (LSU) or a similar SPI diet (dextrose:cornstarch, 0.53:1) formulated by the University of Illinois (UI). Daily gain, average daily feed intake (ADFI), and G:F were increased (P < 0.01) in chicks fed the C-SBM diet relative to chicks fed the two SPI diets, and there were only minor differences between the two SPI diets. In EXP 4, the C x PR and NH x C male chicks were fed the same diets used in EXP 3. Daily gain and ADFI were greater in the C x PR and NH x C chicks fed the C-SBM diet relative to chicks fed the SPI diets (P < 0.01), but the increased average daily gain (ADG) and ADFI in chicks fed the C-SBM diet were much greater in the C x PR chicks (chick x C-SBM vs. SPI, P < 0.01). Daily gain, ADFI, and G:F were greater (P < 0.01) in C x PR chicks than in NH x C chicks. In EXP 5, ADG, ADFI, and G:F were greater (P < 0.04) in chicks fed the C-SBM diet compared with those fed a C-SPC diet. In EXP 6, C x PR chicks fed the C-SBM diet grew faster (P < 0.09) than those fed a rice and casein diet. Variable effects of diet on growth of chicks were affected by breed crosses of chicks.

Effect of different protein sources on growth and carcass traits in growing-finishing pigs.

Crossbred gilts (n = 180) and barrows (n = 180) from the Louisiana State University (LSU) Agricultural Center and the University of Illinois (UI) were used to compare the effect of soybean meal in swine diets, relative to other protein sources, on growth performance and carcass traits of growing-finishing pigs. Four replications with five pigs each at each location were allotted to nine dietary treatments: soybean meal control (SBM), crystalline AA (corn-AA), extruded soybeans (ESB), canola meal (CAN), peanut meal (PNT), sunflower meal (SFLR), ground peas, meat and bone meal (MBM), and poultry by-product meal (PLTY). The diets were formulated to meet or exceed NRC nutrient requirements and to have equal Lys:ME according to dietary phase and sex. Corn was the grain source in all diets and the protein sources were the sole source of supplemental protein in all diets except when AA were added to meet the requirement. Pigs (three per pen at each location) were killed at an average final BW of 114 kg in the LSU or UI Meat Science Laboratories. Pigs fed SBM had greater (P < 0.05) ADG than pigs fed the corn-AA, CAN, SFLR, MBM, or PLTY and greater (P < 0.05) ADFI relative to pigs fed the corn-AA, ESB, MBM, or PLTY. Gain:feed was decreased (P < 0.05) in pigs fed corn-AA or SFLR but increased (P < 0.05) in pigs fed ESB compared with pigs fed the SBM diet. Loin muscle area was decreased (P < 0.05) in pigs fed the corn-AA or MBM diets compared with pigs fed the SBM diet. Tenth-rib backfat thickness was greater (P < 0.10) in pigs fed corn-AA, peas, or MBM than in those fed SBM. The NPPC percentage acceptable quality lean and kilograms of lean were decreased (P < 0.10) in pigs fed corn-AA, peas, or MBM compared with those fed SBM. Results from this experiment suggest that pigs fed SBM have equal or better growth performance and carcass traits than pigs fed other protein sources.

Pinpointing: one method of improving staff compliance with rehabilitation regimens.

This project investigated the effects of a systematic pinpointing and feedback system upon staff follow-through with assignments on a rehabilitation inpatient service. The number and percentage of tasks were recorded over 8 weeks. An ABAB time series reversal design was used where the baseline phases occurred during weeks 1--2 and 5--6, and the intervention occurred during weeks 3--4 and 7--8. Intervention consisted of directing chart round interactions so that assignments were given to specific team members and a list of these tasks was distributed to the team. Results indicated that team performance was significantly affected during intervention weeks. Specifically, the percentage of pinpointing increased from 40% during baseline to an intervention average of 96%. Also, team compliance increased from baseline levels averaging 44% to a mean of 87% during the intervention. The effects of such inexpensive techniques on team effectiveness and the resultant cost benefits to patients in a rehabilitation setting are reviewed.

Dysmenorrhea and personality.

The experiment examined whether reliable personality differences exist between (a) women who suffer from spasmodic and congestive dysmenorrhea and (b) women who experience dysmenorrhea and women who do not. A sample of 12 congestive dysmenorrhea sufferers, 12 spasmodic dysmenorrhea suffers, and 24 nonsufferers obtained from a larger sample of university women, completed the Menstrual Symptom Questionnaire, Minnesota Multiphasic Personality Inventory, Tennessee Self-Concept Scale, and Personality Research Form. Results indicated that congestive sufferers differed from spasmodic sufferers only in their level of impulsivity. However, dysmenorrhea sufferers differed significantly from nonsufferers in that dysmenorrhea sufferers were more similar to a neurotic sample, were depressed, anxious and introverted, and less independent, playful, satisfied with themselves, positive about their physical and social selves than nonsufferers. In spite of these differences, standard scores from the personality measures suggested that dysmenorrhea sufferers were not maladjusted.