Ideal amino acid ratios for sows can be affected by several factors such as the number of fetuses, the number of mammary glands, and stage of gestation for gestating sows and the number of nursing piglets, the number of lactating mammary glands, and maternal tissue mobilization for lactating sows. Earlier work at University of Illinois showed that maternal tissue mobilization contributes large amounts of essential amino acids to milk production and mammary gland growth. However, contributions of threonine and leucine from maternal tissue mobilization are relatively smaller than other essential amino acids. This indicates that a sow with extensive tissue mobilization (first and second parity sows as examples) would require more threonine and leucine than a sow with minimal tissue mobilization (i.e., multiparous sows as examples) during lactation. Ideal amino acid ratios among Lys:Thr:Leu:Val:Arg can change from 100:59:115:77:72 to 100:75:128:78:22 as contributions of amino acids from tissue mobilization increases. Previous work at Texas Tech University and North Carolina State University showed that amino acid uses for fetal and mammary tissue accumulations increase by 19 to 24 fold after d 70 of gestation which increases amino acid needs for sows during late gestation. Moreover, fetal and mammary tissues accrete more leucine and arginine than other essential amino acids increasing needs of leucine and arginine during late gestation when fetal and mammary tissue growth mostly occurs. Increase in the number of fetuses and mammary glands would also increase maternal needs for leucine and arginine. Ideal amino acid ratios among Lys:Thr:Leu:Val:Arg can change from 100:79:88:65:89 to 100:71:95:66:98 as gestation progresses with fetal and mammary tissue growth. Considering dynamic changes in ideal protein for sows, a phase feeding has been suggested for gestating sows whereas a parity feeding has been suggested for lactating sows. It has been difficult to practice phase feeding and parity feeding in sow farms because of limitations with existing feeding systems. Recent advances in feeding systems with multiple feed lines or with abilities of delivering different rations within a barn could allow considering dynamic changes of ideal protein in feeding sows during gestation and lactation.

It is arguable that David Baker significantly defined nonruminant animal nutrition research in the second half of the 20th century with over 450 peer-reviewed publications on a plethora of topics and about 50 PhD students who carry forward his legacy of contributions to the field. At the core of his success was an incredible intellect, a deep and ever-expanding understanding of the intricacies of metabolism and biology, an uncanny awareness of published literature, and a knack for experimental design that yielded unambiguous answers to simple but profoundly important questions. His tools were nonruminant animals—chickens, swine, dogs, cats, and, on rare occasions, rodents. The experiments were built around cleverly designed diets often formulated with purified nutrient sources, reliable, easily measured indicators: growth, efficiency of feed conversion, blood, and tissue parameters. He defied the bioavailability of a several vitamins, mineral elements, and AA in a variety of ingredients, clarified AA interactions and aspects of sulfur AA metabolism in chickens, elucidated the effect of intestinal parasites on nutrient requirements, determined the essentiality of dietary taurine for the feline and the nonessential nature of arginine for gravid swine, and much more. He was driven by a deep love of science and the acquisition of new knowledge, all of which was underpinned by absolute integrity in his work and his dealings with those around him. He was a powerful communicator who enjoyed writing and credited an elementary teacher with his ability to communicate clearly and succinctly. He gave significant priority to mentoring his graduate students as well as many others who sought his advice. David's roots were deeply imbedded in livestock agriculture and he was motivated to do his part to improve the well-being and productivity of the animals with which he worked and the success of those whose livelihood depended on them. By any measure, he was remarkably successful.

A randomized complete-block design was used to evaluate the effects of the ~-adrenergic agonist, cimaterol (CL 263,780), on growth rate, feed efficiency and carcass composition of finishing swine. The drug was fed at four levels (0, .25, .5 and 1.0 ppm) to a total of 240 pigs from 64.5 to 103.7 kg live weight. Growth rate and feed efficiency were measured during the 7-wk feeding trial. Feeding cimaterol depressed feed intake, improved feed efficiency and did not alter rate of gain. Carcass-evaluation showed that pigs continuously fed cimaterol had 13.2, 9.3 and 9.2% less fat measured at the lOth rib, P2 and average backfat (BE) locations, respectively, compared with controls. Cimaterol-fed pigs had increased loin eye areas (10.9%), and increased semitendinosus (11.8%) and biceps femoris (8.9%) weights compared with controls. The semitendinosus muscles of the eimaterol-fed pigs had less fat and the femur bones were shorter and lighter weight than con- trois. There were no detected differences in structural soundness of the live pigs, but postmortem eval- uation of the hooves indicated that pigs fed 1.O ppm cimaterol had a higher incidence of hoof lesions. Pigs withdrawn from cimaterol for 7 d were comparable in performance and carcass characteristics with those continuously fed the drug except that carcass fat measurements had generally returned to control values. The data indicate that cimaterol improved the feed efficiency of finishing pigs and increased the lean:fat ratio of their carcasses. Withdrawal of cimaterol caused compensatory fat deposition.

Twelve multiparous sows (PIC Camb- orough 15; parity >2) were used to investigate the rela- tionship between litter size and day of lactation, and plasma amino acid (AA) arteriovenous differences (A- VD), AA uptake, and plasma flow across the mammary glands. Sows were assigned randomly to one of the following litter sizes: 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, or 14 pigs per litter by cross fostering on d 2 postpartum. All sows were surgically fitted with catheters in the carotid artery and the main mammary vein. Matched arteriovenous blood samples were obtained on d 9, 12, 15, 18, 21, and 24 postpartum. Daily mammary uptake of AA was based on the product of plasma A-VD and daily mammary plasma flow (MPF). Daily MPF was estimated using the Fick method based on lysine con- servation across the gland, and daily milk production. For the majority of AA, as litter size increased, A-VD

A regional experiment was conducted at 8 experiment stations, with a total of 320 sows initially, to evaluate the efficacy of adding 13.35% ground wheat straw to a corn-soybean meal gestation diet for 3 successive gestation-lactation (reproductive) cycles compared with sows fed a control diet without straw. A total of 708 litters were farrowed over 3 reproductive cycles. The basal gestation diet intake averaged 1.95 kg daily for both treatments, plus 0.30 kg of straw daily for sows fed the diet containing ground wheat straw (total intake of 2.25 kg/d). During lactation, all sows on both gestation treatments were fed ad libitum the standard lactation diet used at each station. Response criteria were sow farrowing and rebreeding percentages, culling factors and culling rate, weaning-to-estrus interval, sow BW and backfat measurements at several time points, and litter size and total litter weight at birth and weaning. Averaged over 3 reproductive cycles, sows fed the diet containing wheat straw farrowed and weaned 0.51 more pigs per litter (P <or= 0.04), and had total litter birth and weaning weights that were 0.87 and 3.59 kg heavier (P = 0.01), respectively, than sows fed the control gestation diet. Sows fed the gestation diet containing wheat straw consumed more (P = 0.01) lactation diet per day than control sows. There were no gestation diet treatment differences for any sow fate criterion (farrowing and rebreeding percentages, and culling rate), any sow BW and backfat measurement, or the weaning-to-estrus interval. Lactation diet intake and all sow BW and backfat measurements increased with increasing parity. In conclusion, when the daily intake of the basal gestation diet was equalized for both treatments, the addition of 13.35% ground wheat straw to the gestation diet improved sow and litter performance, with increases in litter size and total litter weight at birth and weaning compared with control sows and litters.

Previous work with growing swine indicated that the lysine requirement, expressed as a percentage of the diet, decreased by .02 percentage units with each 1% reduction in dietary protein level. Thus, the dietary lysine needed for optimal performance may be less than the reported requirement when a portion of the soybean meal in a corn-soybean meal diet is replaced with crystalline lysine. An experiment was conducted to test this concept in each of three phases of growth: growing (23.6 to 47.2 kg), early finishing (47.2 to 74.8 kg) and late finishing (74.8 to 92.8 kg). Dietary crude protein levels were 16, 13 and 12% for the positive control regimen and 14, 11.5 and 11% for the negative control regimen during the growing, early finishing and late finishing periods, respectively. In each phase of growth, regimen 1 was the positive control; regimen 2 was the negative control plus lysine to the level in the positive control; regimen 3 was the negative control plus lysine to the level in the positive control less .02% lysine for each 1% decrease in crude protein from the positive control level; and regimen 4 was the negative control. Ninety-six crossbred pigs were used to form two barrow and two gilts replicates with six pigs per pen-replicate. Average daily gains summarized over the entire growing-finishing period were .74, .75, .75 and .65 kg per day for regimens i, 2, 3 and 4, respectively. Corresponding gain to feed ratios were .29, .29, .30 and .26. Within each growth phase, average

Three experiments were conducted to evaluate the order of limitation for Lys, Thr, and Val in corn-soybean meal diets of lactating sows experiencing high BW loss during lactation. Plasma urea N (PUN) was used as the response criterion. Experimental diets used in all 3 experiments were derived from the basal diet (BSL) formulated to 0.51% Lys using corn and soybean meal as the only sources of AA. The BSL diet was formulated by diluting a reference corn-soybean meal diet (17.2% CP, 0.90% Lys, 0.65% Thr, 0.82% Val, and 0.28% Met) with cornstarch, sucrose, and soybean oil to maintain the same ratio of corn to soybean meal. Experiment 1 was conducted to determine whether PUN is sensitive to dietary Thr and Val levels and whether a 4-d feeding period was adequate to observe a PUN response. The results demonstrated that PUN could be used as the response criterion and that a 4-d feeding period was adequate. Experiment 2 was conducted to determine whether Thr or Val was most limiting in the BSL diet. Dietary treatments used in Exp. 2 consisted of 1) BSL supplemented with 0.09% L-Lys and 0.02% DL-Met, which served as the negative control (NC2); 2) NC2 plus 0.14% L-Thr (NC2 + T); 3) NC2 plus 0.17% L-Val (NC2 + V); and 4) NC2 plus 0.14% L-Thr and 0.17% L-Val (NC2 + T + V). The value for PUN was lower for the NC2 + T and NC + T + V treatments compared with the NC2 and NC2 + V treatments (5.18 and 5.33 vs. 6.43 and 6.62; P < 0.01), indicating that Thr was most limiting in the NC2 diet. Experiment 3 was conducted to determine whether Thr or Lys was most limiting in the BSL diet. Dietary treatments used in Exp. 3 consisted of 1) the BSL diet supplemented with 0.02% DL-Met only, which served as the negative control diet (NC3); 2) the NC3 diet supplemented with 0.20% L-Lys (NC3 + L); 3) the NC3 diet supplemented with 0.14% L-Thr (NC3 + T); and 4) the NC3 diet supplemented with 0.20% L-Lys and 0.14% L-Thr (NC3 + L + T). The value for PUN was lower for NC3 + L compared with NC3 and NC3 + T (7.45 vs. 9.11 and 8.45 mg/dL; P < 0.01), and PUN for NC3 + L + T was lower than the PUN measured for NC3 + L (5.94 vs. 7.45; P < 0.01). The results of Exp. 2 and 3 indicate that Lys was first-limiting and Thr second-limiting in the BSL diet.

Net portal absorption of AA during the 6-h postprandial period was measured in eight gilts (48.5 ± 1.6 kg BW) in a crossover design. The pigs had chronic catheters placed in the portal vein, carotid artery, and ileal vein, and were trained to consume 1.2 kg of a standard grower diet once daily. Blood samples were taken every 30 min for 4 h and then hourly until 6 h after feeding. The first set of blood samples was taken after pigs were fed a meal of the test 16% CP corn–soybean meal diet (16% CP) or the test 12% CP corn–soybean meal diet supplemented with crystalline lysine, threonine, and tryptophan (12% CP + AA) to equal the three AA levels in the 16% CP diet. Pigs were then fed the standard diet for 2 d. Following that, blood samples were again taken after the pigs were fed a meal of the test diet that was not given to them at the first sampling period. Net portal AA absorption was calculated by multiplying porto-arterial plasma AA concentration difference by portal vein plasma flow rate (PVPF), estimated by an indicator-dilution technique employing p-aminohippuric acid as the indicator infused into the ileal vein. Plasma concentrations of lysine and threonine of pigs were affected by the diet × time interaction (P < 0.01). Portal and arterial plasma lysine and threonine concentrations in pigs attained the maximal level by 1 h postprandial when the 12% CP + AA diet was fed, but reached the peak level at 2.5 h postprandial when the 16% CP diet was given. The PVPF of pigs over the 6 h postprandial was less (P < 0.01) when the 12% CP + AA diet was given than when the 16% CP diet was fed. Net portal absorptions of lysine and threonine also were affected (P < 0.05) by time × diet interaction. The peak portal absorption of both lysine and threonine in pigs appeared at 0.5 h postprandial when the 12% CP + AA diet was given, but at 2.5 h postprandial with the feeding of the 16% CP diet. The early appearance of peak portal absorption of lysine and threonine from feeding the 12% CP + AA compared with the 16% CP diet indicates that crystalline lysine and threonine are absorbed more rapidly than protein-bound lysine and threonine in pigs fed once daily.

The objective of this study was to determine whether soybeans without the Kunitz trypsin inhibitor and lectins could be fed effectively to young chicks and pigs. Specifically, we compared the growth performance of chicks and pigs fed diets containing modified soybeans: Kunitz trypsin inhibitor-free (KF), lectin-free (LF), lectin and Kunitz trypsin inhibitor-free (LFKF), conventional soybeans (CSB), and commercially obtained, dehulled, solvent-extracted soybean meal (SBM). A 7-d chick experiment was conducted to evaluate the nutritional value of CSB, KF, LF, LFKF, and SBM. The experiment was conducted as a completely randomized design, with four replicates, five treatments, and six male chicks per pen (n = 120). The five treatments consisted of 23% CP dextrose-soybean-based diets containing KF, LF, LFKF, CSB, or SBM as the source of dietary protein. A 28-d pig experiment was conducted to evaluate the nutritional value of CSB, LF, LFKF, and SBM. Pens of four pigs were assigned randomly to a control, corn-SBM, or one of six corn-soybean diets containing raw or extruded soybean varieties as a 2 x 3 factorial arrangement of treatments in a randomized complete block design with five blocks per treatment (n = 140). Chicks fed diets containing any of the raw soybean varieties gained less weight (P < 0.05) than chicks fed SBM (22.81 g/d for SBM vs. 14.17 g/d for the raw soybeans combined). Among the raw soybean treatments, there was a greater effect on growth performance (P < 0.05) by removing both lectins and Kunitz trypsin inhibitor (ADG of 16.56 g for LFKF) than by removing each antinutritional factor separately (ADG of 14.38 and 14.11 g for KF and LF, respectively). Pig growth performance was different (P < 0.001) for SBM (ADG of 409 g) and all the varieties when extruded (ADG of 450 g for CSB, 417 g for LF, and 408 g for LFKF) compared with the raw soybean treatments (ADG of 101 g for CSB, 165 g for LF, and 266 g for LFKF). Among the raw soybean treatments, growth performance improved (P = 0.003) as the antinutritional factor, lectin, was removed from the soybean and improved further (P = 0.045) when both lectins and Kunitz trypsin inhibitor were removed. The growth-inhibiting effect of feeding modified soybeans to young animals was more detrimental for pigs than for chicks in our experiments. Soybeans without the Kunitz trypsin inhibitor and lectins cannot be fed successfully to young chicks and pigs without heating.

Introduction Profitability in the swine industry is based on prolificacy. One measurement of prolificacy is the number of piglets produced per year. To optimize prolificacy and profits it is essential that sows are re-bred as soon as possible after weaning. An extended post-weaning anestrus decreases overall productivity and increases costs of production. A large number of sows undergo prolonged postpartum anovulatory periods. Furthermore a significant number of sows, after having their first litter never return to estrus and are removed from the herd. Many factors influence the duration of the weaning-to-estrous interval including: parity, season, duration of lactation, breed and nutritional status (Kirkwood et al.,1984; Aherne and Kirkwood, 1985; Clark et al., 1986; Dial et al., 1987).

Three experiments were conducted to test the hypothesis that supplementing nursery pig diets with a mixture of carbohydrases (CS) will improve pig performance and nutrient digestibility. The CS used in these experiments contained 7 units/g of alpha-1,6-galactosidase, 22 units/g of beta-1,4-mannanase, beta-1,4 mannosidase, and trace amounts of other enzymes. In Exp. 1, 108 pigs weaned at d 21 of age were fed one of three diets containing 0 (control), 0.1, or 0.2% CS for 5 wk, based on a three-phase feeding program (1, 2, and 2 wk). Over the entire 35-d period, ADG was not affected (P > 0.05) by treatment, but supplementing 0.1% CS increased (P < 0.05) gain:feed by 9%. Experiment 2 used 10 gilts fitted with simple T-cannula in the terminal ileum at 3 wk of age. After cannulation, pigs were fed the same control Phase I and II diets, but the Phase III diet contained either 0 or 0.1% CS. Ileal samples were collected for the 3 d following the 5-d adjustment period during Phase III. Apparent ileal digestibility of GE, lysine, threonine, and tryptophan was greater (P < 0.05) in the CS diet. In Exp. 3, 90 pigs weaned at 21 d of age were fed the same control Phase I and II diets, but the Phase III diet contained either 0 or 0.1% CS. Phase III diets were fed for 3 wk. Average daily gain of the CS group was greater (P < 0.05) than the control group during wk 3. Gain:feed ratio was greater (P < 0.05) for the carbohydrase group during the entire Phase III period. Four pigs per treatment were killed at the end of Exp. 3 to measure villus height and to determine the concentration of raffinose and stachyose in different parts of the gastrointestinal tract. Average villus height was greater (P < 0.05) in pigs fed the CS diet. Carbohydrase supplementation decreased (P < 0.05) the concentration of stachyose in freeze-dried digesta from the proximal and distal small intestine. Raffinose concentration, on the other hand, was decreased (P < 0.05) by CS supplementation only in the distal small intestine. These lower concentrations suggest that CS improved the digestibility of carbohydrate in soybean meal. In conclusion, the addition of CS to Phase I and Phase II nursery diets containing low levels of soybean meal did not improve pig performance, but its addition to corn-soybean meal-based Phase III nursery diets improved gain:feed ratio and energy and AA digestibility.

Forty-eight barrows were used in a 2 x 6 factorial arrangement to test a hypothesis that feeding a protein-deficient diet affects subsequent growth response by altering the efficiency of protein utilization. Barrows were individually fed either a 9% crude protein (CP) diet or an 18% CP diet from 20 to 30 kg of body weight (BW) (depletion phase). From 30 to 45 kg BW (realimentation phase), pigs were fed one of six experimental diets with CP levels of 11.8, 13.1, 14.3, 15.6, 18.8, and 21.8%. Four pigs were slaughtered at 20 kg BW to determine initial body composition. Four pigs from each treatment in depletion phase (a total of eight) were slaughtered at 30 kg BW, and all pigs from each treatment in realimentation phase (a total of 36) were slaughtered at 45 kg BW for subsequent compositional analysis. Pigs were bled at 20, 30, and 40 kg BW for blood urea nitrogen (BUN), insulin-like growth factor (IGF)-I, and IGF-binding protein (IGFBP) assays. Pigs were given three times the maintenance digestible energy requirement (3 x 120 kcal BW(-0.75) x d(-1)) in three equal meals daily. The feed allowance was adjusted every 3 d. During the depletion phase, pigs fed the 18% CP diet grew faster and more efficiently (P < 0.01) and gained more (P < 0.01) water and protein than did pigs fed the 9% CP diet. Pigs fed the 18% CP diet showed higher (P < 0.01) BUN values, IGF-I concentrations, and IGFBP ratios than pigs fed the 9% CP diet. During the realimentation phase, pigs fed the 9% CP diet during the depletion phase grew faster (P < 0.05), tended to grow more efficiently (P = 0.066), gained more water (P < 0.01), and tended to gain more protein (P = 0.068) than pigs fed the 18% CP diet during the depletion phase. Pigs fed the 9% CP diet during the depletion phase tended (P = 0.069) to have a higher protein requirement during the realimentation phase than pigs fed the 18% CP diet during the depletion phase. When measured at 40 kg BW, pigs fed the 9% CP diet had a lower (P < 0.05) BUN than pigs fed the 18% CP diet during the depletion phase. However, the plasma IGF-I concentration and IGFBP ratio at 40 kg BW were not affected by dietary CP level fed during the depletion phase. This study indicates that pigs fed a protein-deficient diet exhibit compensatory growth. During the period of compensatory growth, the requirement of CP for those pigs is higher than that of pigs previously fed an adequate diet. This study also suggests BUN can be used as an indicator of protein utilization efficiency and compensatory growth.

Two experiments were conducted to determine the effects of feeding reduced-CP, AA-supplemented diets at two ambient temperatures (Exp. 1) or three levels of dietary NE (Exp. 2) on pig performance and carcass composition. In Exp. 1, 240 mixed-sex pigs were used to test whether projected differences in heat increment associated with diet composition affect pig performance. There were 10 replications of each treatment with four pigs per pen. For the 28-d trial, average initial and final BW were 28.7 kg and 47.5 kg, respectively. Pigs were maintained in a thermoneutral (23 degrees C) or heat-stressed (33 degrees C) environment and fed a 16% CP diet, a 12% CP diet, or a 12% CP diet supplemented with crystalline Lys, Trp, and Thr (on an as-fed basis). Pigs gained at similar rates when fed the 16% CP diet or the 12% CP diet supplemented with Lys, Trp, and Thr (P > 0.10). Pigs fed the 12% CP, AA-supplemented diet had a gain:feed similar to pigs fed the 16% CP diet when housed in the 23 degrees C environment but had a lower gain:feed in the 33 degrees C environment (diet x temperature, P < 0.01). In Exp. 2, 702 gilts were allotted to six treatments with nine replicates per treatment. Average initial and final BW were 25.3 and 109.7 kg, respectively. Gilts were fed two levels of CP (high CP with minimal crystalline AA supplementation or low CP with supplementation of Lys, Trp, Thr, and Met) and three levels of NE (high, medium, or low) in a 2 x 3 factorial arrangement. A four-phase feeding program was used, with diets containing apparent digestible Lys levels of 0.96, 0.75, 0.60, and 0.48% switched at a pig BW of 41.0, 58.8, and 82.3 kg, respectively. Pigs fed the low-CP, AA-supplemented diets had rates of growth and feed intake similar to pigs fed the high-CP diets. Dietary NE interacted with CP level for gain:feed (P < 0.06). A decrease in dietary NE from the highest NE level decreased gain:feed in pigs fed the high-CP diet; however, gain:feed declined in pigs fed the low-CP, AA-supplemented diet only when dietary NE was decreased to the lowest level. There was a slight reduction in longissimus area in pigs fed the low-CP diets (P < 0.08), but other estimates of carcass muscle did not differ (P > 0.10). These data suggest that pigs fed low-CP, AA-supplemented diets have performance and carcass characteristics similar to pigs fed higher levels of CP and that alterations in dietary NE do not have a discernible effect on pig performance or carcass composition.

The study was conducted to determine the effects of feeding a 16% CP diet, a 12% CP diet, or a 12% CP diet supplemented with crystalline Lys, Trp, and Thr (12% CP + AA diet) in a thermal-neutral (23 degrees C) or heat-stressed (33 degrees C) environment on various body and physiological measurements in growing pigs. Heat-stressed pigs were given a 15% lower daily feed allowance than thermal-neutral pigs to remove the confounding effect of feed intake caused by high temperature. No diet x temperature interaction was observed for any variables (P > 0.09) except for pig activity and pancreas weight. At 33 degrees C, pig activity and pancreas weight did not differ among dietary treatments (P > 0.05). In contrast, at 23 degrees C, pigs fed the 12% CP diet had greater activity than those fed the 16% CP diet or the 12% CP + AA diet (P < 0.05). Pancreas weight was greater for pigs fed the 12% CP + AA diet than those fed the 12% CP diet (P < 0.05) when maintained at 23 degrees C. Compared with 23 degrees C, the 33 degrees C temperature decreased pig activity, heat production, daily gain, feed efficiency, and affected the concentration and accretion of empty body protein and ash, as well as weights of heart, pancreas, stomach, and large intestine (P < 0.05). Pigs fed the 12% CP + AA diet attained similar levels of performance and rates of empty body water, protein, lipid, and ash deposition as pigs fed the 16% CP diet (P > 0.10). Pigs fed the 12% CP + AA diet had lower serum urea plus ammonia nitrogen concentrations (P < 0.01) and total heat production (P < 0.05) compared with those fed the 16% CP diet or the 12% CP diet. These results confirm that, with crystalline AA supplementation, growing pigs fed a 12% CP diet will perform similar to pigs fed a 16% CP diet. The data further indicate that lowering dietary CP and supplementing crystalline AA will decrease total heat production in growing pigs whether they are housed in a thermal-neutral or heat-stressed environment.

An experiment involving 25 experiment stations in the North Central and Southern regions (NCR-42 and S-288, respectively) was conducted to assess the degree of uniformity of diet mixing among stations and to assess the variability among station laboratories in chemical analysis of mixed diets. A fortified corn-soybean meal diet was mixed at each station using a common diet formula (except for vitamin and trace-mineral additions). The diet was calculated to contain 14% crude protein (CP), 0.65% Ca, 0.50% P, and 125 ppm Zn (based on 100 ppm added Zn). After mixing, samples were collected from the initial 5% of feed discharged from the mixer, after 25, 50, and 75% was discharged, and from the final 5% of discharged feed. The five samples were sent to the University of Kentucky, finely ground, and divided into subsamples. Each set of five subsamples from each station was distributed to three randomly selected stations for analysis of CP, Ca, P, and Zn (i.e., each station analyzed five diet sub-samples from three other stations). In addition, two commercial and two station laboratories analyzed composites of the five subsamples from each of the 25 mixed diets. Based on the laboratories that analyzed all diets, means were 13.5, 0.65, and 0.52%, and 115 ppm for CP, Ca, P, and Zn, respectively. Ranges of 11.8 to 14.6% CP, 0.52 to 0.85% Ca, 0.47 to 0.58% P, and 71 to 182 ppm of Zn were found among the 25 diet mixes. The coefficients of variation among the 25 diet samples for CP, Ca, P, and Zn were 4.3, 9.3, 4.1, and 17.4%, and among the 25 laboratories were 3.6, 12.5, 10.7, and 11.1%, respectively. Overall analyses of the five sub samples were, respectively, CP: 13.4, 13.6, 13.4, 13.5, and 13.4% (P < 0.06); Ca: 0.66, 0.67, 0.67, 0.66, and 0.67%; P: 0.50,0.51,0.51,0.50, and 0.50%; and Zn: 115, 116, 112, 113, and 120 ppm (P < 0.001). Diets were not uniformly mixed at all stations (station x sample No. was P < 0.08 for Ca and P < 0.01 for CP, P, and Zn). Among stations, the range of the five samples, expressed as a percentage of the mean and averaged for CP, Ca, P, and Zn, varied from +/- 1.1% (i.e., 98.9 to 101.0%) to +/- 12.9% (84.6 to 110.4%), with an overall average of +/- 5.2%. Neither type nor volume of mixers was related to mixing uniformity. The results suggest that uniformity of diet mixes varies among experiment stations, that some stations miss their targeted levels of nutrients (especially Zn), and that the variability among experiment station laboratories in analysis of dietary Ca, P, and Zn in mixed diets is quite large.

Twelve multiparous sows (PIC Camborough 15; parity >2) were used to investigate the relationship between litter size and day of lactation, and plasma amino acid (AA) arteriovenous differences (A-VD), AA uptake, and plasma flow across the mammary glands. Sows were assigned randomly to one of the following litter sizes: 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, or 14 pigs per litter by cross fostering on d 2 postpartum. All sows were surgically fitted with catheters in the carotid artery and the main mammary vein. Matched arteriovenous blood samples were obtained on d 9, 12, 15, 18, 21, and 24 postpartum. Daily mammary uptake of AA was based on the product of plasma A-VD and daily mammary plasma flow (MPF). Daily MPF was estimated using the Fick method based on lysine conservation across the gland, and daily milk production. For the majority of AA, as litter size increased, A-VD did not increase, except for alanine (P < 0.05, linear and quadratic) and valine (P < 0.1; trend; linear and quadratic). As day of lactation increased, A-VD for the majority of AA increased (P < 0.05, linear and quadratic) except for arginine, lysine, and phenylalanine. As litter size increased, net daily mammary AA uptake increased for all indispensable AA (P = 0.001 to P < 0.05, linear and quadratic), excepting arginine. Milk production increased with increasing litter size (P < 0.001, linear) and with increasing day of lactation (P < 0.05, quadratic). Daily MPF increased (P < 0.05, linear) with increasing litter size, but did not change during the period measured from d 9 to 24. In conclusion, litter size appears to be a major determinant of net mammary AA uptake with daily mammary plasma flow a driving variable, whereas AA A-VD is a function of day of lactation and a major variable in determining net AA uptake with advancement of lactation.

Twenty-eight primiparous sows were used to study nutrient mobilization among body tissues as influenced by litter size in lactating sows. Litter size was set to 6, 7, 8, 9, 10, 11, or 12 pigs within 48 h postpartum by cross-fostering. Four sows were allotted to each litter size group. Sows had 11.5 +/- 1.3 Mcal of ME and 39.3 +/- 4.4 g of lysine per day and were killed on d 20.6 +/- 1.1 of lactation. Liver, gastrointestinal tract (GIT, composed of the empty stomach, empty small and large intestines, cecum and rectum), reproductive tract, and other organs (excluding liver, GIT, reproductive tract, and mammary gland) were separated from the carcass. Gastrointestinal tracts were manually stripped of contents and flushed with water to remove digesta. Hot carcasses were split longitudinally at the midline after removing mammary glands and internal organs. Individual organs and carcasses were weighed then ground for chemical analysis. Dry matter, crude protein, fat, and ash contents were measured. As litter size increased, protein mobilization was linearly increased (P < 0.05) in carcass, GIT, and reproductive tract. Protein mobilization in liver was quadratically affected by litter size (P < 0.05). Fat mobilization was not affected by litter size. The amount of protein mobilized from carcass, GIT, liver, and reproductive tract in sows increased by 641 g as litter size increased by one pig from 6 to 12 pigs after a 21-d lactation. Carcass contributed the largest amount of protein (600 g for an additional pig) among body tissues, whereas the reproductive tract contributed the highest percentage (26%) of its protein among body tissues. Protein efficiency from milk to litter weight gain was 72% as litter size increased during a 21-d lactation. In feeding lactating sows, effect of litter size on nutrient mobilization from various tissues should be considered for minimizing the excess tissue mobilization during lactation.