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The present study evaluated growing mink () as a model for dietary protein quality assessment of protein meals used in extruded dog foods. Three foods with similar CP content but of different protein quality were produced using different protein meals. The protein meals varied with respect to CP digestibility and AA composition and included lamb meal (LBM), poultry meal (PM), and fish meal (FM) with low, intermediate, and high protein quality, respectively. Nitrogen balance, BW gain, protein efficiency ratio (PER), and apparent total tract digestibility (ATTD) were used as measures of protein and AA bioavailability in growing mink. Standardized ileal digestibility (SID) was used to measure protein and AA bioavailability in adult dogs (). The mink study (3 × 3 Latin square design) included 12 kits aged 8 to 11 wk. The dog study included 12 dogs divided in 3 groups allocated to 1 of the experimental diets. The growing mink responded in accordance with the different AA supply between diets, as determined by the first limiting AA. The LBM diet deviated from the other diets with lower ( < 0.001) values for N retention, BW gain, and PER, and the diets differed ( < 0.001) in ATTD of CP and all AA, except for hydroxyproline. Retention of N was 0.66, 1.04, and 1.18 g·kg·d; BW gain was 8.2, 26.8, and 35.3 g/d; PER was 0.38, 1.39, and 1.71; and ATTD of CP was 66.8, 73.8, and 82.1% for the LBM, PM, and FM diets, respectively. In dogs, SID of CP and AA differed ( ≤ 0.017) between diets and was generally lowest for the LBM diet, intermediate for the PM diet, and greatest for the FM diet. For CP, SID was 71.5, 80.2, and 87.0% for the LBM, PM, and FM diets, respectively. The contents of digestible CP and AA (based on SID) covered the minimal requirement for adult dogs set by the NRC for all diets, except for the content of digestible Met + Cys in the LBM diet. Despite this, dietary content of Met + Cys in the LBM diet agreed with the recommended level set by the NRC and the Association of American Feed Control Officials for adult dogs but was below the level recommended by the European Pet Food Industry Federation. It was concluded that growth studies with mink kits can provide valuable information in protein quality assessment of extruded dog foods. Furthermore, the study showed that to ensure nutritional adequacy of dog food and to be able to compare protein quality of dog foods, information on AA composition and digestibility is crucial.

The objectives of this study were to determine the chemical composition and nutritive value of corn protein product 1 (CPP 1), corn protein product 2 (CPP 2), and corn fiber (CF), novel coproducts of the ethanol industry, and compare these feed ingredients with standard plant protein ingredients [soybean meal (SBM), distillers dried grains with solubles (DDGS), corn gluten meal (CGlM), and corn germ meal (CGeM)], and to compare CF sources (CF control 1 and control 2) with standard fiber sources (peanut hulls, Solka-Floc, and beet pulp) commonly used in pet foods. Corn fiber, CPP 1, and CPP 2 were produced at a pilot-scale modified dry-grind plant, with CPP 2 having a greater degree of purification than CPP 1. Crude protein values for CPP 2 and CPP 1 were 57.3 and 49.7%, respectively. Total dietary fiber concentration was 29% for CPP 2 and 23.5% for CPP 1. Acid-hydrolyzed fat and GE concentrations were similar for these ingredients. In a protein efficiency ratio assay, no differences (P > 0.05) in feed intake, BW gain, or CP intake were noted for CPP 2, CPP 1, or CGlM. However, feeding CPP 2 resulted in a greater (P < 0.05) G:F ratio and protein efficiency ratio than CPP 1 and CGlM. In a cecectomized rooster assay, CGlM had numerically the greatest standardized total AA, total essential AA, and total nonessential AA digestibilities, but they were not different (P > 0.05) from CPP 1 or SBM values. Corn germ meal resulted in the least values, but they were not different from those for DDGS and CPP 1. The greatest values for true nitrogen-corrected ME were obtained with CGlM, followed by CPP 2, DDGS, CPP 1, SBM, and CGeM. Distillers dried grains with solubles and CPP 1 had similar true nitrogen-corrected ME values, and they were not different from values for CPP 2 and SBM. In vitro CP disappearance was greatest (P < 0.05) for CGlM (94.1%), intermediate for DDGS (76.8%) and CPP 1 (77.5%), and least for CPP 2 (74.1%) and CGeM (67.7%). Corn fibers contained predominantly insoluble dietary fiber (1% or less of soluble dietary fiber), with a moderate CP concentration. In vitro OM disappearance for the fiber sources, when using inoculum from dog feces, revealed that with the exception of beet pulp, which had a moderate disappearance value after 16 h of fermentation (17.7%), all fiber substrates had a nonsignificant extent of fermentation. In conclusion, novel corn coproducts had properties comparable with the standard protein and fiber sources used in animal nutrition.

Several experiments were conducted to evaluate the protein quality of various raw and rendered animal by-product meals commonly used in companion animal diets. Six freeze-dried raw animal meals (beef lungs, pork lungs, sheep lungs, pork livers, oceanfish, chicken necks) and 3 rendered animal meals (lamb meal, regular ash poultry by-product meal, and low ash poultry by-product meal) were fed in chick assays to determine Lys and TSAA bioavailability, protein efficiency ratio (PER), and net protein ratio (NPR). Each experimental diet was offered to 4 replicates of 5 chicks per pen in all growth assays. Furthermore, each animal by-product meal was fed to mature White Leghorn roosters for determination of true AA digestibility. All freeze-dried, raw animal meals were offered to 5 replicate roosters, and all rendered animal meals were offered to 4 replicate roosters. Most raw animal meals exhibited moderate to high protein quality. Lysine bio-availabilities ranged from 86 to 107% and 70 to 99% for raw and rendered animal meals, respectively. Bio-availability of TSAA ranged from 64 to 99% and 61 to 78% for raw and rendered animal meals, respectively. The PER values ranged from 2.83 to 4.03 and 2.01 to 3.34 for raw and rendered animal meals, respectively. The NPR values ranged from 3.83 to 4.8 and 3.05 to 4.12 for raw and rendered animal meals, respectively. Despite a numeric increase in NPR vs. PER values, the overall ranking of animal meals remained similar. Lamb meal had the poorest PER and NPR values, and pork lungs had the greatest values. Total essential AA digestibility and total AA digestibility ranged from 93.6 to 96.7 and 90.3 to 95.5%, respectively, for raw animal meals and 84.0 to 87.7 and 79.2 to 84.8%, respectively, for rendered animal meals. Rendered animal meals generally had lower protein quality than raw animal meals, with lamb meal consistently having the poorest protein quality and pork livers having the greatest protein quality.

An experiment to determine the chemical composition and protein quality of 13 fish substrates (pollock by-products, n = 5; fish protein hydrolysates, n = 5; and fish meals, n = 3) was conducted. Two of these substrates, salmon protein hydrolysate (SPH) and salmon meal with crushed bones (SMB), were used to determine their palatability as components of dog diets. Pollock by-products differed in concentrations of CP, crude fat, and total AA by 71, 79, and 71%, respectively, and GE by 4.1 kcal/g. Fish protein hydrolysates and fish meals were less variable (approximately 18, 14, and 17%, and 1.4 kcal/g, respectively). Biogenic amine concentrations were much higher in fish protein hydrolysates as compared with pollock by-products and fish meals. Pollock liver and viscera had the highest total fatty acid concentrations; however, red salmon hydrolysate and SMB had the highest total PUFA concentrations (49.63 and 48.60 mg/g, respectively). Salmon protein hydrolysate had the highest protein solubility in 0.2% KOH. Based on calculations using immobilized digestive enzyme assay values, lysine digestibility of fish meal substrates was comparable to in vivo cecectomized rooster assay values and averaged approximately 90.3%. Also, pollock milt, pollock viscera, red salmon hydrolysate, and sole hydrolysate had comparable values as assessed by immobilized digestive enzyme assay and rooster assays. A chick protein efficiency ratio (PER) assay compared SMB and SPH to a whole egg meal control and showed that SMB had high protein quality (PER = 3.5), whereas SPH had poor protein quality (PER value less than 1.5). However, using whole egg meal as the reference protein, both fish substrates were found to be good protein sources with an essential AA index of 1.0 and 0.9 for SMB and SPH, respectively. In the dog palatability experiments, a chicken-based control diet and 2 diets containing 10% of either SPH or SMB were tested. Dogs consumed more of the SPH diet compared with the control, and similar amounts of the SMB and control diets. The intake ratios for each were 0.73 and 0.52, respectively. Salmon protein hydrolysate was especially palatable to dogs. These data suggest that chemical composition and nutritional quality of fish substrates differ greatly and are affected by the specific part of the fish used to prepare fish meals and fish protein hydrolysates.

The chemical composition and protein quality of 11 alternative protein sources (chicken products, blood products, enzyme-hydrolyzed fish protein concentrate, soybean meal, and spray-dried pork liver) were determined, and an experiment was conducted to determine palatability and digestibility of processed red blood cell-containing diets. Chicken protein sources differed in concentrations of CP, acid-hydrolyzed fat, and total AA (TAA) by 20, 31, and 24%, respectively, and GE by 1.7 kcal/g. Blood protein sources varied little in acid-hydrolyzed fat and GE concentrations, but concentrations of CP and TAA differed by 11 and 8%, respectively. Protein solubility of chicken and blood protein source categories averaged 57 and 69%, respectively. Protein solubility of enzyme-hydrolyzed fish protein concentrate, soybean meal, and spray-dried pork liver was 53, 67, and 26%, respectively. Based on calculations from immobilized digestive enzyme assay values, lysine digestibility averaged approximately 80.4 and 81.7% for blood and chicken protein sources, respectively. Lysine digestibility values for soybean meal and spray-dried pork liver were 89 and 77%, respectively. A chick protein efficiency ratio (PER) assay showed that chicken protein sources had high protein quality values, as the PER ranged from 2.7 to 5.3, whereas blood protein sources had poor protein quality (PER values less than 1.5). Enzyme-hydrolyzed fish protein concentrate, spray-dried pork liver, and soybean meal had high protein quality (PER values greater than 2.8). In the dog palatability and digestibility experiments, a corn and chicken-based diet supplemented with either 0 or 3% processed red blood cells was tested. The palatability test showed that dogs consumed more of the diet that contained 0% vs. 3% processed red blood cells. The intake ratio for the 3% processed red blood cells diet was 0.34. Nutrient digestibilities did not differ, except for CP, where the digestibility was greater (P = 0.01) for dogs consuming the 0% processed red blood cells diet. These data suggest that chemical composition and quality of alternative protein sources differ greatly among ingredients within the same category. Palatability data suggest that a processed red blood cells-containing diet is not highly palatable but, when this diet was offered as only one food, dogs demonstrated no aversion response but some decrease in protein digestion.

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.

Economically viable options for retaining ownership of spring-born calves through a winter backgrounding program are somewhat limited in the southeastern United States. Although sod-seeded winter annual forages produce less forage than those same forages planted using conventional tillage practices, sod-seeded winter annual forages have the potential to provide a low-cost, rapid-gain, ecologically and economically viable option for retaining ownership of fall-weaned calves. A study was conducted during the winters of 1998, 1999, and 2000 using 180 crossbred calves (261 +/- 2.8 kg initial BW; n = 60 each year) to compare sod-seeded winter annual forages with conventional hay and supplement backgrounding programs in southeast Arkansas. Calves were provided bermudagrass hay (ad libitum) and a grain sorghum-based supplement (2.7 kg/d) on 1-ha dormant bermudagrass pastures or were grazed on 2-ha pastures of bermudagrass/dallisgrass overseeded with 1) annual ryegrass, 2) wheat plus annual ryegrass, or 3) rye plus annual ryegrass at a set stocking rate of 2.5 calves/ha. Calves grazed from mid-December until mid-April but were fed bermudagrass hay during times of low forage mass. Mean CP and IVDMD concentrations were 19.0 and 71.1%, respectively, across sampling dates and winter annual forages, but three-way interactions among forage treatments, year, and sampling date were detected (P < 0.01) for forage mass, concentrations of CP, and IVDMD. The IVDMD of rye plus ryegrass was greater (P < 0.05) than that of ryegrass in yr 2. A forage treatment x sampling date interaction was detected for forage CP in yr 1 (P < 0.05) and 2 (P = 0.05) but not in yr 3 (P = 0.40). Forage mass did not differ (P > or = 0.22) among winter annual treatments on any sampling date. During the first 2 yr, calves fed hay plus supplement gained less (P < 0.05) BW than calves that grazed winter annual forages; gains did not differ (P > or = 0.23) among winter annual treatments. During the 3rd yr, undesirable environmental conditions limited growth of the winter annual forages; total gain did not differ (P = 0.66) among the four treatments. Winter annual forages offer potential to provide high-quality forage for calves retained until spring, but consistent forage production and quality are a concern when sod-seeding techniques are used.

The influence of extrusion cooking on the protein content, amino acid profile, and concentration of antinutritive compounds (phytic acid, condensed tannins, polyphenols, trypsin, chymotrypsin, alpha-amylase inhibitors, and hemagglutinating activity) in kidney bean seeds (Phaseolus vulgaris L. var. Pinto) was investigated. Growing male rats were fed diets based on casein containing raw or extruded kidney beans with or without methionine supplementation for 8 or 15 d. Rates of growth, food intake, and protein efficiency ratio were measured and the weight of the gastrocnemius muscle and the composition of its nitrogenous fraction was determined. Extrusion cooking reduced (P < 0.01) phytic acid, condensed tannins, and trypsin, chymotrypsin, and (alpha-amylase inhibitory activities. Furthermore, hemagglutinating activity was abolished by extrusion treatment. Protein content was not affected by this thermal treatment. Rats fed raw kidney bean lost BW rapidly and the majority died by 9 d. Pretreatment of the beans by extrusion cooking improved food intake and utilization by the rats and they gained BW. Supplementation of extruded kidney bean with methionine further enhanced (P < 0.01) food conversion efficiency and growth. However, BW gains and muscle composition still differed (P < 0.01) from those of rats fed a high-quality protein.

We conducted three studies with steers to evaluate poultry by-product meal (PBM) as a supplemental N source for ruminants. An in situ study compared the solubility, degradation rate, and ruminal escape of PBM N with blood meal (BM), corn gluten meal (CGM), and soybean meal (SBM) N. Additionally, an 84-d growth study (n = 95, 228+/-5 kg BW) and a digestion trial (6 x 6 Latin square) were conducted. The basal diet for the growth and digestion studies consisted of 49% corn silage, 36% cottonseed hulls, and 15% supplement (DM basis). Sources of supplemental N (% of total supplemental N) were 100% SBM and 0, 25, 50, 75, and 100% PBM, with urea used to balance for N. In situ ruminal escape N (25.2, 55.3, 86.7, and 98.9% for SBM, PBM, CGM, and BM, respectively) was greater (P < .05) for PBM than for SBM; however, a greater (P < .05) proportion of BM and CGM N escaped ruminal degradation compared with PBM. Dry matter intake, ADG and gain/ feed increased linearly (P < .003) as PBM increased; however, no differences (P > .48) were observed in these variables for 100% PBM compared with 100% SBM. Duodenal N flow and small intestinal N disappearance increased linearly (P < .05) as PBM increased in the diet. Bacterial N flow to the small intestine was not affected (P > .19) by treatment; however, 100% SBM decreased (P < .04) bacterial CP synthesis (g bacterial N/kg OM disappearance from the stomach) compared with 0 and 100% PBM. In vivo ruminal escape N of PBM and SBM was 40.6 and 13.7%, respectively. Ruminal NH3 N decreased linearly (P < .001) as PBM increased. These data suggest that PBM can replace SBM as a source of supplemental N for steer calves that consume a diet based on corn silage and cottonseed hulls.

We evaluated feather meal (FTH) and poultry by-product meal (PBM) as complementary protein sources for growing calves. In a replicated 84-d growth trial, individually fed steer calves (n = 120; 252 +/- 24 kg) were supplemented with urea or with graded levels of soybean meal (SBM), FTH, PBM, or 2/3 FTH:1/3 PBM (CP basis). Protein efficiency, calculated as gain above the urea control vs natural protein intake using the slope-ratio technique, was greater for FTH than for SBM, PBM, and 2/3 FTH:1/3 PBM (P < .10). Addition of ruminally protected methionine and lysine did not affect protein efficiency (P > .30) for FTH, PBM, or 2/3 FTH:1/3 PBM. Even though true protein digestibility in the gastrointestinal tract in a trial with lambs was similar (P > .15) for FTH (83.1%) and PBM (91.2%), escape protein was greater for FTH (66.8%) than for PBM (43.6%). Analyses were conducted to estimate intestinal flow of amino acids relative to requirements for live animal gain, and no obvious amino acid deficiencies were present. The lack of a response in protein efficiency to ruminally protected methionine and lysine suggests that FTH and PBM are adequate in these amino acids. Although FTH and PBM are excellent sources of metabolizable protein, there was no complementary response in protein efficiency between them.

We conducted two studies to assess the protein and energy value of pearl millet grain (Pennisetum glaucum [L.] R. Br.) for mature goats. In Exp. 1, 15 2-yr-old male castrated goats were gradually introduced over a 4-mo period to three all-grain diets consisting of 100% corn (Zea mays L.), 50:50 corn:pearl millet, and 100% pearl millet. After the adjustment to all-grain feeds, the goats were fed the diets in metabolism crates for 2-d adjustment and 7-d total collection periods. For Exp. 2, complete diets containing the three grain treatments (corn, 50:50 corn:pearl millet, and pearl millet) as 40% of the total DM as fed (the remainder was mainly alfalfa meal and mineral supplement) were balanced to contain 16% crude protein (CP) and 2.24 Mcal digestible energy (DE)/kg on an air-dry basis. Twelve mature (4- to 6-yr-old) buck goats were randomly assigned to diets and fed in pens for 14 d and then moved to metabolism crates for 10-d adjustment and 10-d total collection periods. In Exp. 1, DM intake was unaffected by dietary treatment, but digestibility of DM and organic matter was lowest (P < .10) in goats fed 100% pearl millet. Digestibility of complete diets also decreased (P < .10) as corn was replaced by 50 or 100% pearl millet, but DM intake increased (P < .10) on the 100% millet diet. In both experiments, substituting pearl millet for corn had no effect on nitrogen retained by the goats. Metabolizable energy of pearl millet was only 92% that of corn, but ME intake was similar when the grains were fed as 40% of the dietary DM. Pearl millet has potential as a major energy feed for goats in areas where it can be economically produced.

In Exp. 1, six steers (254 kg) were used in a 6 x 4 incomplete Latin square to determine the effects of solvent-extracted soybean meal alone or in combination with rumen-protected methionine and lysine on N balance in steers limit-fed a high-corn diet to gain 1.1 kg/d. The basal diet contained (DM basis) 80% rolled corn, 15% alfalfa, and .9% urea (13.9% CP), and 2 or 4% soybean meal replaced corn to give CP concentrations of 14.8 and 15.6%, respectively. Each diet was fed with and without 5 g/d of Smartamine-ML (.75 and 2.0 g of rumen-protected methionine and lysine, respectively). Nitrogen retention increased linearly (P = .09) with level of soybean meal. Rumen-protected methionine and lysine had no effect on N balance. In Exp. 2, seven steers (233 kg) were used in a 7 x 4 incomplete Latin square experiment to investigate optimal levels and sources of CP for steers limit-fed to gain 1 kg/d. Treatments included a negative-control diet (urea; 11.7% CP) and six diets containing either 13.5, 15.4, or 17.2% CP with either solvent-extracted or expeller-processed soybean meal. Diets provided 75, 87.5, 100, or 112.5% of estimated CP requirement for a gain of 1 kg/d. The basal diet contained 83% rolled corn, 15% alfalfa, and .2% urea. Nitrogen retention increased linearly (P = .006) with soybean meal addition, and no differences were observed between CP sources. The CP system underpredicted the protein requirements of limit-fed steers under our conditions.

Goats generally tolerate dry season forage conditions in northeastern Brazil's tropical deciduous woodland better than sheep do, but the mechanisms underlying sheep and goat response to wet and dry season conditions are not well understood. We evaluated aspects of nutrition and behavior of free-ranging sheep and goats in this woodland to improve our understanding of these mechanisms. Body weight changes, dietary botanical and chemical composition, and daily activities were measured for sheep and goats that foraged in this woodland during four defined periods of a year. Vegetation available to these animals was also measured. Although there was much less available vegetation during the wet season than during the dry season, body weights and dietary crude protein content of sheep and goats increased during the wet season and decreased during the dry season. During the four periods of the year, weight changes of sheep, and possibly those of goats, were positively related to the content of crude protein in their diets. Foraging times of sheep and goats were generally greater during the dry season than during the wet season and were positively related to available browse and inversely related to dietary crude protein content. Sheep and goats may have foraged longer during the dry periods because they were spending more time searching through the large quantity of low-quality vegetation for dietary items with relatively higher levels of crude protein.

The feed intake pattern and growth performance of boars, barrows, and gilts fed diets differing in lysine and protein content were measured on 120 crossbred pigs from 27 (SD 3.7) to 81.5 (SD 9.2) kg live weight. The pigs were housed in eight mixed-sex groups with five pigs of each sex in each group. They were fed from an electronic feed station that recorded individual meal sizes and the time and duration of visits to the feeder for each animal in the group. Four dietary treatments were compared. During the grower period (27 to 55 kg), diets ranged in lysine content form .98 to 1.31%; for the remainder of the study, lysine content was .88 to 1.18%. Barrows had a greater (P < .01) number of meals per day than the other two sexes (7.4 vs 7.0 vs 7.0 +/- .10, respectively), but there were no significant differences among sexes for daily feed intake or other feed intake traits. Daily feed intake increased with dietary lysine content, largely because of increased meal sizes resulting from longer feeder occupation times at each visit. Visits to the feeder were greatest between 0900 and 1100 and lowest between 2000 and 0400. Correlations between feeding pattern and growth traits were relatively low. Repeatabilities of feeding pattern traits were generally higher when measured over shorter time periods. These results suggest a change in feeding behavior with increasing dietary lysine levels and a relatively small effect of sex on feeding pattern for mixed-sex groups of 15 pigs fed from a single electronic feed station.

Little progress has been made in modeling intake regulation in spite of the many mechanisms identified as important. A model with relatively simple inputs was developed that included compartments for protein, soluble carbohydrate, digestible fiber, and very slowly digesting fiber. Distention and chemostatic feedbacks were combined using a previously published equation. The ratio of current ruminal fill to a modulating parameter for ruminal fill represented distention feedback. The ratio of the current flow of available energy to a modulating parameter for chemostatic demand represented chemostatic feedback. The modulating parameter for ruminal fill was based on literature reports of ruminal contents. Intake was adjusted based on current fill and energy flow relative to modulating parameters for fill and chemostatic feedback. The effect of the digestible organic matter (DOM) to CP ratio on DOM intake was modeled to adjust rates of digestion, rates of passage, and the chemostatic feedback. The model tested an integrated concept of intake regulation with only CP, IVDMD, and NDF as inputs. In spite of relatively simple inputs, the model behavior in response to variation in protein, digestibility, and fiber was similar to observations of animal responses.

Consulting nutritionists were surveyed to determine current formulation and management practices for finishing beef cattle. Among the six consultants surveyed, percentage of CP in finishing diets ranged from 12.5 to 14.4%, with urea levels ranging from .5 to 1.5% of DM. Finishing diets were based primarily on highly processed, rapidly fermented grains (steam-flaked and high-moisture grain), with roughage levels ranging from 3 to 11% of DM. All six consultants considered feed bunk management to be a critical factor affecting feed intake and performance; five of the six consultants used aggressive implant programs based on estrogen + trenbolone acetate. Recent university research was reviewed with respect to CP level and source in finishing diets. Finishing cattle managed on aggressive implant programs seem to respond to higher levels of CP better than would be expected from the factorial calculation approach. Moreover, improvements in performance noted in recent research seemed to be more consistent when supplemental CP was derived from ruminally degraded vs undegraded sources. Calculation of protein requirements with a metabolizable protein (MP) system yielded estimates of protein needs by finishing cattle that agreed more closely with current industry practices than did calculation based on the factorial method. The difference between the MP system and the factorial method was primarily a result of accounting for microbial N needs in the MP system. Reasons for production responses to CP levels that are greater than those calculated by the factorial method include increased accretion of protein by rapidly growing, implanted cattle, particularly during the initial phase of the finishing period, alleviation of a microbial N deficiency, and ruminal and systemic effects of ruminally degraded N on acid-base balance of beef cattle fed rapidly fermented, high-grain diets. Reasons for production responses to supplemental CP need further research.

Four Holstein steers (222 kg) with cannulas in the rumen and proximal duodenum were used in a crossover design experiment to evaluate the energy and protein value of dehydrated poultry excreta (DPE). Dietary treatments contained (DM basis) 4% alfalfa hay, 8% sudangrass hay, 49% flaked barley, 8% cane molasses, 3% yellow grease, .8% urea, 1.4% limestone, .3% mineral salt, and .4% chromic oxide, plus 25% of either tapioca pellets or DPE. The DPE contained 42% ash and 27% CP (6% true protein). Substituting DPE for tapioca decreased the DE value of the diet (P < .01). The estimated DE value of the DPE was 1.36 Mcal/kg (.34 Mcal NEm/ kg). There were no treatment effects (P > .10) on microbial N flow to the small intestine or ruminal microbial efficiency (grams of microbial N/kilogram of OM fermented). The addition of DPE increased (P < .05) the flow of non-ammonia and feed N to the small intestine. The estimated ruminal escape N value of DPE was 22%, although very little of this was true protein. Dehydrated poultry excreta did not increase (P > .10) flow of alpha-amino N to the small intestine. Ruminal degradability of uric acid was 96%. Total tract true digestibility of N in DPE was 84%. It is concluded that the NE value of DPE is markedly overestimated in current tables of feeding standards. Less than 10% of the N in DPE escapes the rumen as true protein N.

'Surrey' ryegrass (Lolium multiflorum Lam.) has produced well in clipping yield trials across Louisiana, but yield trials do not always predict how well the forage supports performance under grazing conditions. This trial compared Surrey ryegrass with 'Marshall' ryegrass grazed continuously or rotationally. Two pastures of Surrey and two pastures of Marshall that had been subdivided into six paddocks each were used in 2 yr. Yearling steers grazed the pastures. In the 1st yr, pastures within a cultivar were either continuously or rotationally grazed. Thus, animal performance on the rotationally grazed treatments was unreplicated and the data were not included in the statistical analysis. In the 2nd yr, each pasture contained both continuous and rotational groups of cattle. Cattle gains for the two cultivars were not different in either yr 1 (P > .26) or yr 2 (P > .17). In yr 2, continuous grazing allowed for greater individual animal gains (P = .03) than rotational grazing. However, the lower stocking rate of continuously grazed paddocks resulted in a decreased pasture gain (P = .001) of 301 compared with 403 kg/ha for the rotationally grazed paddocks. Forage quality was not different between Surrey and Marshall ryegrass, but there was a tendency (P = .12) for Surrey to have less forage mass during yr 1. Overall, continuously grazed paddocks had lower CP and NDF and higher in vitro true digestibility than rotationally grazed paddocks. Surrey was equivalent to Marshall ryegrass in animal performance and quality, and continuous grazing provided higher individual animal performance but lower performance on a gain per hectare basis than rotational grazing.

Swine growth models have the potential to evaluate alternative management decisions and optimize production systems. However, the lack of economical, yet accurate methods to obtain the growth parameters required to characterize pig genotypes, and which are required by growth models, limits their widespread implementation. The four primary parameters required are 1) daily whole-body protein accretion potential, 2) partitioning of energy, intake over maintenance between protein and lipid accretion, 3) maintenance requirements for energy, and 4) daily feed intake. Estimation of daily protein accretion rates requires that serial estimates of composition and growth be fitted to flexible nonlinear functions. Serial dissection and chemical analysis are too expensive to be routinely conducted on an adequate number of pigs for precise daily protein accretion rates at different live weights. Three alternate methods include 1) serial slaughter and double sampling; 2) use of serial live measurements to estimate composition, i.e., serial ultrasonic measurements; and 3) use of generalized functions that estimate daily protein accretion as a function of mean daily fat-free lean gain over a specified weight interval. The energy partitioning between lipid and protein accretion can be expressed as two interchangeable measurements, either as the slope of protein accretion or the change in the lipid: protein gain ratio as a function of energy intake at each live weight. Both methods require serial estimates of composition and scale feeding of pigs to specified energy intake levels. Maintenance requirements for energy are better expressed as a function of protein mass than body weight. However, differences in body protein mass do not fully explain difference in maintenance requirements between various pig genotypes. Daily feed intakes at each live weight can be estimated by accurately collecting feed intake data at least three live weight ranges and fitting the data to nonlinear functions. An alternative method to estimate daily feed intake is to develop daily lipid and protein accretion curves. On the basis of their energetic costs of lipid and protein deposition and assumed maintenance requirements, daily energy intakes can be estimated. Genetic selection changes the underlying growth parameters. The selection criteria and testing environment direct the relative genetic change for each growth parameter. The different sexes may also be affected differently by selection. For this reason, each closed uniformly selected population must be evaluated for each parameter for each sex.

Hydrolyzed feather meal (FM) was compared to other sources of CP to determine its value as a protein source in a molasses-based liquid supplement. Ruminal N escape values (measured in situ) for FM, ring-dried blood meal, cottonseed meal, and soybean meal approximated reported values. Ruminal N escape value for catfish meal was lower than values reported for other fish meals. In two trials (194 d), 84 yearling heifers were allotted to 12 pastures (3 pastures/treatment) and fed one of four supplements (1.7 kg of DM.heifer-1.d-1) containing either molasses and urea; molasses, urea,and FM; molasses, urea, FM, and catfish meal; or molasses, urea, FM, and catfish oil. Heifers were exposed to bulls for 60 d. In two trials, 112 steers were allotted to 16 pastures (4 Pastures/treatment) and fed one of four supplements (1.7 kg of DM.steer-1.d-1) containing molasses and urea; molasses, urea and FM; molasses, urea, FM and ring-dried poultry blood meal; or molasses, urea, and poultry feathers and blood hydrolyzed together. In all trials, cattle fed molasses containing FM had faster gains (P < .05) and heifers had heavier live weights at breeding (P < .05) and higher pregnancy rates (P < .05) than cattle fed molasses and urea. Combining poultry blood with molasses, urea, and FM improved (P < .05) steer gains in one of two trials. Combining catfish meal with molasses, urea, and FM did not improve (P > .05) ADG of pregnancy rate of heifers. Combining catfish oil with molasses, urea, and FM increased (P < .05) ADG in one trial and blood cholesterol and live weight of heifers at breeding in both trials. It is concluded that protein feeds, such as FM, that contain a large portion of ruminally undegradable protein may provide much of the CP in liquid supplements fed to growing cattle consuming moderate-quality forage. Adding catfish oil to a liquid supplement may improve ADG and live weight of yearling heifers at breeding.

The experiment had two objectives: 1) to determine the protein requirements of two strains of growing-finishing pigs based on growth performance, carcass characteristics, tissue accretion rates, and organ weights and 2) to evaluate whether protein requirements can be determined from changes in plasma urea concentration. Forty-six Gene Pool (GP) and 46 Hampshire (H) gilts with an initial BW of 28.5 kg were used. Pigs were allotted to two trials of a randomized complete block experiment with a 2 x 6 factorial arrangement of treatments. Five pigs from each strain were randomly selected and slaughtered at the beginning of each of the two trials. The remaining 72 pigs were individually penned and allotted to one of six dietary treatments (10, 13, 16, 19, 22, or 25% CP). Pigs remained on the experiment until the mean weight of a treatment group within each strain reached 115 kg (16 wk for GP and 14 wk for H), at which time all pigs of that strain were slaughtered. The only strain x protein level interactions that were detected were for carcass protein and water accretion rates. Gene Pool pigs grew less rapidly and utilized feed less efficiently than H pigs (P < .001). Average daily gain (quadratic, P < .05) and ADG/ADFI (quadratic, P < .05) were increased as protein level increased until a plateau was reached. Backfat depths were decreased (linear, P < .001) and longissimus muscle areas were increased (linear, P < .001) as protein level increased. Protein accretion rate was lower (P < .01) and fat accretion was higher (P < .01) in GP pigs than in H pigs. Protein accretion increased (quadratic, P < .001) and fat accretion decreased (linear, P < .001) with increasing dietary protein level. Examination of the response of plasma urea concentration over time suggested that GP pigs required 13% CP from 30 to 80 kg and 10% CP thereafter, whereas H pigs required 19% CP from 30 to 45 kg, 16% CP from 45 to 100 kg, and 13% CP thereafter.

Forages help meet the protein requirements of ruminants by providing degraded CP for microbial protein synthesis plus protein that escapes ruminal degradation. Evidence from numerous feeding studies with lactating dairy cows indicates that excessive ruminal protein degradation may be the most limiting nutritional factor in higher-quality temperature legume forages. Hence, there is interest in identifying factors that influence the rate and extent of ruminal degradation of forage proteins. Condensed tannins found in legumes are known to decrease protein degradation, either by altering the forage proteins or by inhibiting microbial proteases. Quadratic regressions of degradation rate and estimated protein escape on tannin concentration reached minimal rate (.048/h) and maximal escape (56%) at 27 g of tannic acid equivalents/kg of DM. Although most tannin-containing forages are not well-adapted to growing conditions in North America, biotechnology has been used to inject genes for tannins into adapted germplasm. The CP in red clover, which has no detectable tannins, was found to be less degradable than that in alfalfa, both in the silo and in the rumen. Small differences in protein degradability also were detected among alfalfa germplasm. Protein in alfalfa harvested as hay, rather than as silage, was used more efficiently for milk protein synthesis when fed to lactating cows; degraded CP from hay was captured more efficiently by ruminal microbes for protein synthesis in vitro. A ruminal escape of approximately 35% for total dietary CP is recommended by the NRC for lactating dairy cows fed mixed diets with 1.6 to 1.7 Mcal of NE1/kg of DM. Ruminal degradation of CP from the forage portion of the diet can exceed 65% when forages are the major source of degradable protein. When ruminants obtain most or all of their nutrients from forage, the ruminal escape for forage protein should approximate 35%.

This experiment was conducted to determine the relationship between 3-methylhistidine (3MH) production and proteinase activity in skeletal muscles of growing barrows. Barrows at 13 wk of age were randomly assigned to either control diet available on an ad libitum basis (21% of ME consisted of protein; control group), control diet fed restricted (pair-fed with barrows in protein-free group; intake-restricted group), or protein-free diet available on an ad libitum basis (protein-free group) for 14 d. During the last 3 d, blood samples were collected for determination of 3MH production rate, which is a measure of myofibrillar protein breakdown. At slaughter, two muscles were taken: masseter (M) and longissimus (L) muscles. The muscle samples were analyzed for calpastatin, mu-calpain, m-calpain, multicatalytic proteinase (MCP), cathepsin B, cathepsins B+L, and cystatins activities. Both muscles were also analyzed for amounts of DNA, RNA, total protein, and myofibrillar and sarcoplasmic proteins. Growth rate (kilograms/day) was influenced by dietary treatments (P < .05). Fractional breakdown rate (FBR, percentage/day) of skeletal muscle, as calculated from 3MH production rate (micromoles.kilogram-1.day-1), was 27% higher for the protein-free group than for the control group. However, no differences in proteinase activities were observed, except for lower MCP activity in the M muscle of the protein-free group than in that of the other groups (P < .05). In the present study, no direct relation was observed between myofibrillar protein degradation rate and proteinase activities in skeletal muscle during a protein-free feeding strategy.

Thirty wether lambs (52.5 +/- 1.5 kg) were used in a replicated 3 x 5 factorial treatment arrangement and four periods to determine dietary intake and digestibility of three ground forages with increasing levels of supplemental ground corn. Forages were a mature, low-protein grass hay (LQH; 5.2% CP), an immature, medium-protein grass hay (MQH; 10.2% CP), and an immature, high-protein grass hay (HQH; 14.2% CP). Supplementation treatments were no supplement (NS), a protein supplement (PS), protein plus .25% BW of corn (LC), protein plus .5% BW of corn (MC), and protein plus .75% BW of corn (HC). Crude protein intake (1.4 g/kg BW) from supplements was equalized with soybean meal and corn gluten meal. Lambs were housed in metabolism crates. Supplements were fed at 0700 each morning after orts from the previous day's feeding were removed. Hay was subsequently offered at approximately the previous day's consumption plus 25%. Each of the four periods lasted 21 d. Sixteen days were allowed for diet adaptation. Feces were collected with fecal bags during d 17 to 21. Lambs receiving LQH and PS had higher forage (P < .04) and total DMI (P < .001) than lambs fed LQH and NS. Corn supplementation decreased forage intake (quadratic effect; P = .08), total intake (quadratic effect; P = .08), and increased apparent DM digestibility (linear effect; P < .04) with lambs receiving LQH. Protein supplementation did not affect forage or total DMI (P > .11), and corn supplementation did not affect total DMI (P > .20) with either MQH or HQH.(ABSTRACT TRUNCATED AT 250 WORDS)

In Trial 1, 240 crossbred steers (initial BW 243 +/- 8 kg) were used in a 2 x 4 factorial experiment to determine the effects of receiving diet CP concentration (12, 14, 16, or 18%) and source (spray-dried blood meal [SDBM] vs soybean meal [SBM]) on steer performance. There were linear (P < .01) increases in ADG and feed efficiency during wk 1. For the entire trial, there was an increase (P < .01) in feed efficiency with increasing CP concentration and diets containing SDBM compared with those containing SBM. In Trial 2, 240 crossbred steers (initial BW 246 +/- 14 kg) were used in a completely randomized design experiment to determine the effects of receiving diet CP concentration (11, 14, 17, 20, 23, or 26%) on steer performance. Average daily gain and feed efficiency increased (P < .01) with increasing CP concentration during wk 1. There were quadratic (P < .01) responses to CP concentration for final weight, ADG, and feed efficiency. In Trial 3, 216 steers (initial BW 238 +/- 1 kg) were used to determine the effects of receiving diet protein sources on steer performance. The control diet used SBM as the supplemental CP source and was formulated to contain 12.5% CP. The other five protein sources were corn gluten meal (CGM), ring-dried blood meal (RDBM), SDBM, fish meal (FM), and SBM. For these five CP sources, diets were formulated to contain 23% CP during wk 1, 17% CP during wk 2, and 12.5% CP during wk 3 and wk 4. During wk 1, control steers had the lowest ADG (P < .07) and feed efficiency (P < .01) whereas steers fed RDBM and SDBM had the highest (P < .01) feed efficiency. Increased CP concentrations are needed early in the receiving period, when DMI is low.

Eight dual flow continuous culture fermenters were used in four replicated periods to study the effects of protein supplements on ruminal fermentation and CP digestion. A basal diet was supplemented with isonitrogenous amounts of urea and tryptone (control; CTRL), soybean meal (SBM), lignosulfonate-treated SBM (LSBM), corn gluten meal (CGM), blood meal (BM), hydrolyzed feather meal (HFM), fish meal (FM), or meat and bone meal (MBM). Digestion of DM, OM, and carbohydrates was not affected by treatment. Ammonia N concentration was highest (P < .05) for CTRL and lowest (P < .05) for LSBM, CGM, BM, HFM, and FM. Nonammonia N flow was lowest (P < .05) for CTRL. Dietary N flow was lowest (P < .05) for CTRL, intermediate for SBM, and highest (P < .05) for LSBM, CGM, BM, HFM, FM, and MBM. Total N flow, bacterial N flow, and efficiency of microbial protein synthesis were not affected by treatment. Protein degradation was highest (P < .05) for CTRL. Flow of total amino acids (AA) was lowest (P < .05) for CTRL, SBM, and MBM. Diets containing BM provided the largest (P < .05) amounts of essential AA and lysine, and FM provided the largest (P < .05) amounts of methionine in fermenter effluent. Supplementation of diets with proteins low in ruminal degradability increased flows of nonammonia N, dietary N, and total and essential AA and modified the AA profile flowing out of fermenters.

We studied the effects of supplement CP concentration on performance and forage use of cattle allowed ad libitum access to ammoniated wheat straw. During two consecutive winters, crossbred beef cows in late gestation (n = 87 in 1990-1991, n = 84 in 1991-1992) were used in a randomized complete block design with three pens per treatment. Cows were stratified by weight, body condition score (BCS), age, and breed and randomly assigned within strata to 1) control (C, no supplement), or 2 kg/d of 2) low-protein (LP) supplement (12% CP), 3) moderate-protein (MP) supplement (20.1% CP), or 4) high-protein (HP) supplement (31.7% CP) (DM basis). The feeding period was 84 d in 1990-1991 and 60 d in 1991-1992. Supplementation (C vs LP, MP, or HP) increased (P < .01) cow weight gains (32.7 vs 60.7, 62.8, and 72.4 kg, respectively) and improved (P < .01) BCS. Calf birth weights, weaning weights, and ADG were not affected by treatment (P > or = .20). Average calving date, percentage of cows cycling at the start of the breeding season and percentage pregnant after a 60-d breeding season were also similar (P > .20) among treatments. Sixteen ruminally fistulated steers (482 kg, four steers per treatment) were blocked by weight and assigned to the same four supplements in a 30-d digestion trial. Supplementation increased (P < .01) digestible DMI and forage DMI (P < or = .04) and tended (P = .09) to increase digestible NDF intake but did not alter (P > or = .15) apparent DM or NDF digestibility.(ABSTRACT TRUNCATED AT 250 WORDS)

Holstein-Friesian bull calves were fed diets of three metabolizable energy concentrations: 11.7, 10.9, and 10.0 MJ/kg of DM, and the same content of CP, 145 g/kg. Two trials were carried out. Initial weights were 195 and 180 kg and final weights were 490 and 600 kg for Trials 1 and 2, respectively. The live weight gains (kg/d) were .93, 1.06, and 1.16 in Trial 1 and .98, 1.11, and 1.16 in Trial 2 on the low-, medium-, and high-energy diet, respectively. In Trial 2, measurements were made of ruminal fluid volume and urea space, which expresses the protein mass in the body. Ruminal fluid volume of young calves was high, exceeding 250 mL/kg live weight. Proportional to live weight, it tends to decrease from the age of 213 d to slaughter. It was higher on the lower-energy diet (P < .01). Rate of fat deposition between 250 and 600 kg body weight did not increase even on the diet with 11.7 MJ/kg, although these calves were fatter (P < .05) at slaughter than those on the low-energy diets. The ratios of depot fats (g of fat/kg of hot carcass) in both trials were close for each energy level, in spite of a 100-kg difference in live weight at slaughter. It was 24.0, 29.8, and 40.7 for calves fed low-, medium-, and high-energy diets, respectively, in Trial 1 and 27.7, 37.1, and 40.4, respectively, in Trial 2.(ABSTRACT TRUNCATED AT 250 WORDS)

The effects of supplemental fish meal on site and extent of digestion were determined using four steers equipped with ruminal, duodenal, and ileal cannulas. Fish meal was included in diets to supply 0 (0FM), 25 (25FM), 50 (50FM), or 75 (75FM) g of N daily above the CP requirement of a 400-kg steer gaining 1.2 kg/d. Total tract starch digestibility tended to be greatest for 25FM (95%), lowest for 0FM (90%), and intermediate for 50FM (94%) and 75FM (92%). Total tract N digestibility was greatest for 25FM, lowest for 0FM, and intermediate for 50FM and 75FM (cubic, P < .05). Total tract starch digestibility increased .46 percentage units for each unit increase in N digestibility (n = 16, P = .03). Ruminal starch digestibility was greatest for 25FM, intermediate for 50FM and 75FM, and lowest for 0FM (quadratic; P < .10). Starch flow to the duodenum was decreased for 25FM and 50FM vs 0FM and 75FM (quadratic, P < .10) and N flow to the duodenum was increased (linear, P < .01) by fish meal. Fish meal supplementation increased N digestibility (quadratic, P < .05) but had no effect (P > .10) on starch digestibility in the small intestine. Starch digestibility in the small intestine was not related to N flow to the duodenum; however, starch digestibility increased .9 percentage units for each percentage unit increase in N digestibility (n = 16, P = .02). Fish meal supplementation tended to increase total tract starch digestibility by increasing ruminal, but not small intestinal, digestibility.

An experiment was conducted to evaluate the effect of feeding reduced CP, amino acid (AA)-supplemented diets to pigs from weaning to slaughter weight on growth performance and carcass characteristics. Pigs were fed a 19%-16%-14% CP starter-grower-finisher high-CP sequence of diets, respectively, or a sequence of diets reduced in CP by 4 percentage units (3 percentage units in the finisher period) with or without lysine (LYS), tryptophan (TRP), and threonine (THR) supplementation. Pigs fed the low-CP diets without AA supplementation grew more slowly, were less efficient in feed conversion, and developed carcasses that contained a smaller longissimus muscle, greater, average backfat depths, and a lower percentage of muscle compared with pigs fed the high-CP sequence of diets (P < .01). The reduction in growth performance, feed efficiency, longissimus muscle area, and percentage of muscle in pigs fed the low-CP diets was alleviated by LYS, TRP, and THR supplementation (P > .10). Although pigs fed the low-CP diets supplemented with AA had reduced average and 10th rib backfat depths compared with pigs fed the unsupplemented, low-CP diets (P < .01), these fat depth measures remained greater (P < .05) than those of pigs fed the high-CP diets. Feeding reduced dietary CP, regardless of AA supplementation, resulted in reduced heart (P < .10) and liver weights (P < .01) compared with feeding the high-CP diets.(ABSTRACT TRUNCATED AT 250 WORDS)

Postweaning gain performance and individual feed intake on 271 Hereford and 263 Angus bulls were recorded during three 168-d test periods from 1984 to 1986. Each breed was composed of two lines and within each breed bulls were fed either a high-energy (HD) or a medium-energy (MD) diet. Energy intake was partitioned into energy for maintenance and growth based on predicted individual animal requirements. Estimates of heritability were obtained using Restricted Maximum Likelihood with an individual animal model including fixed effects of year, diet, and covariates of initial weight and backfat change by breed and with line effects for overall data. Bulls fed the HD grew faster and had higher metabolizable energy intake per day (MEI), residual feed consumption (RFC), and gross and net feed efficiency (FE and NFE) (P < .001) than those fed the MD. Estimates of heritability for Hereford and Angus bulls, respectively, were .46 and .16 for 200-d weaning weight (WWT), .16 and .43 for average daily gain (ADG), .19 and .31 for intake per day (MEI), .43 and .45 for yearling weight (YWT), .07 and .23 for RFC, .08 and .35 for FE, and .14 and .28 for NFE. Genetic and phenotypic correlations between MEI and ADG, MEI and YWT, ADG and YWT, ADG and FE, YWT and FE, and FE and NFE were moderately to highly positive for both breeds. Negative genetic and phenotypic correlations between NFE and ADG show partial correlations of FE with ADG after accounting for energy requirement for maintenance. Residual feed consumption was negatively associated with YWT, FE, and NFE, indicating a possible genetic improvement.

Three trials evaluated the protein and energy value of high-lysine corn for finishing calves. In Trial 1, 60 finishing steer calves were used to evaluate corn source (high-lysine vs control) and protein source (urea, blood meal [BM], corn gluten meal [CGM]) and level (BM and CGM addition; low, medium, high). Calves were individually fed using Calan gates for 102 d, and then were pen-fed (two pens per corn treatment) the remaining 83 d. During the initial 102 d, calves fed high-lysine corn had similar gains but were 6% more efficient (P < .10) compared with calves fed control corn. Performance did not differ (P > .10) among sources or levels of protein supplementation. Over the entire feeding period (185 d), calves fed high-lysine corn were 10% more efficient (P < .10) than calves fed control corn. In the second study, in situ starch disappearance was faster (P < .10) and the proportion of CP degraded by 12 h was 27% greater (P < .10) for high-lysine corn than for control corn. In a metabolism trial, five steers fitted with ruminal, duodenal, and ileal cannulas were used in a randomized block design to evaluate the effect of corn source on site and extent of digestion. Intake and ruminal and total tract digestibility of OM and N did not differ (P > .10) between corn sources. Steers fed high-lysine corn tended to have greater ruminal (P = .23) and postruminal (P = .18) starch digestion, resulting in greater (P < .10) total tract starch digestibility.(ABSTRACT TRUNCATED AT 250 WORDS)

Sixteen light horse mares (8 to 9 yr of age; 457 to 579 kg BW) were fed Bermudagrass hay and a corn/cottonseed hull-based supplement formulated to contain either 100% (control) or 50% (restricted) of the protein and(or) energy requirements for maintenance in a 2 x 2 factorial arrangement of treatments. Daily measurements of intake, BW, and plasma hormones and metabolites were made for 33 d. Plasma glucose, insulin, NEFA, and urea N were measured in hourly samples drawn on d 27, and parallel with an i.v. glucose tolerance test (IVGTT) and epinephrine challenge on d 29. Energy restriction increased daily NEFA concentrations (P < .001) and urea N (P = .013), whereas protein restriction decreased (P = .002) urea N concentrations. These effects of protein and energy restriction occurred within 24 h and were consistent (day effect, P > .1) throughout the remaining 24 d. Normal meal consumption elevated plasma glucose, insulin, and urea N concentrations (time effect, P < .08). Plasma NEFA concentrations did not change after feeding in mares fed control energy, but decreased in mares fed restricted energy (energy x time interaction, P = .005). After IVGTT, areas under the curve for plasma glucose and insulin were smaller in mares fed restricted protein (P < .05), whereas glucose area was larger in mares fed restricted energy (P = .009). After epinephrine injection, energy restriction increased the initial magnitude of the NEFA response, but after 50 min, reduced plasma NEFA below pre-injection concentrations (energy x time interaction, P = .06).(ABSTRACT TRUNCATED AT 250 WORDS)

Accurate prediction of forage biological values and performance with animals fed forages requires accurately accounting for factors that influence animal requirements and feedstuff utilization. The Cornell Net Carbohydrate and Protein System (CNCPS) is an application model that uses a combination of mechanistic and empirical approaches to account for the effects of variation in animal factors and feed carbohydrate and protein fractions on animal performance. Thus, accurate animal and environmental descriptions, DMI, feed carbohydrate, and protein fractions and their digestion rates are required inputs. In 25 growth periods with calves fed high-forage diets, the CNCPS accounted for 74, 81, and 83%, respectively, of the variation in ADG predicted to be supported by the ME, metabolizable protein, and essential amino acid intake, the first-limiting of all three accounting for 81% of the variation with a -1% bias. Thus, the CNCPS can be used to accurately describe forage quality and the effects of changes in forage composition on animal performance. The model was sensitive to variations in NDF, CP, protein solubility, NDF and starch digestion rates, feed and microbial amino acid composition, maintenance protein requirement, body protein amino acid content, and the coefficient of efficiency of use of absorbed protein. Analysis of several trials indicates an improved efficiency of ME use with improved amino acid balances. Uses of the CNCPS discussed include interpreting, planning and applying research, teaching, developing tables of requirements and biological values for feeds, complex nutritional accounting, and predicting performance and profits.

Two calf corn-residue grazing trials were conducted to evaluate the effect of supplementing with two alfalfa hays (Medicago sativa), varying in their amount of CP and ADF, with and without escape protein (EP). In Trial 1, heifers (204 kg) grazed (1.36 heifers/ha) non-irrigated fields for 92 d. No difference (P > .05) in ADG was found when medium-protein (16.3% CP) and high-protein (18.0% CP) alfalfa hays were provided at 2.7 kg of DM.heifer-1.d-1. In Trial 2, 60 steers (257 kg) were supplemented individually with medium-protein (17.6% CP) alfalfa hay, 1.86 (MPL) and 2.27 kg DM (MPH), and one level of high-protein (18.7% CP) alfalfa hay, 1.86 kg DM (HPL). In a 2 x 3 factorial arrangement of treatments, steers were fed with or without EP (113 g.steer-1.d-1 from blood meal and corn gluten meal). Steers grazed a non-irrigated corn residue field (2.58 steers/ha) for 57 d and were watered and individually supplemented overnight. Diet quality and composition was estimated by collecting extrusa samples twice each week using four esophageally fistulated steers. No effects of alfalfa protein content or level (P > .05) were reflected in gain: 357, 309, and 326 g.steer-1.d-1 for steers receiving MPL, MPH, or HPL alfalfa treatments, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)

Five trials investigated the feeding value of wet and dried corn distillers byproducts as a source of protein and energy for growing and finishing cattle and investigated the effect of heat damage on the feeding value of dried distillers byproducts. In a calf growth trial, no differences in rate of gain or protein efficiency were observed among calves fed wet distillers byproducts (wet distillers grains + thin stillage; WDB) or one of three composites of dried distillers grain + solubles (DDGS) having a low, medium, or high concentration of ADIN. A finishing trial compared the energy value of dry-rolled corn (DRC) with WDB or the three DDGS composites, fed at 40% of the diet DM replacing DRC. Cattle consuming WDB or DDGS gained faster (P < .05) and more efficiently (P < .05) than cattle fed DRC. Although gains were similar, cattle fed WDB consumed less feed (P < .10) and were more efficient (P < .10) than cattle fed DDGS. Level of ADIN in DDGS did not affect efficiency of gain (P > .10). In a lamb finishing trial, the addition of 5 or 10% ethanol did not affect (P > .10) daily gain, DMI, or feed efficiency. In two metabolism trials with steers, grain byproducts (wet distillers grains, dry distillers grains plus solubles, wet corn gluten feed, dry corn gluten feed, hominy feed) and DRC had similar effects on ruminal pH and total VFA. Feeding thin stillage or condensed solubles reduced (P < .10) ruminal pH and tended to reduce acetate:propionate. Wet corn distillers byproducts, fed at 40% of the diet DM, contain more NEg than did DRC and drying WDB reduces its NEg content. Acid detergent insoluble N is a poor indicator of protein and energy value in distillers grains.

Two trials were conducted to determine the adequacy of ADIN as an indicator of N digestibility. In Trial 1, eight nonforage plant protein sources were heated at 150 degrees C for 90 min in the presence of xylose (12.8% of CP, DM basis) to produce heat damage. Thirty-four wethers (average BW 40 kg +/- 9.9) were used to determine the effect of heat on N digestibility. Differences in ADIN were evident among the protein sources, and no significant heat x protein source interaction was observed for N digestibility. Apparent N digestibilities were reduced (P < .001) for all protein sources by heat treatment. Acid detergent insoluble N and N digestibility were correlated (r2 = .66). However, the assumption that ADIN was completely indigestible led to underestimation of N digestibility: approximately 58% of the ADIN was digestible in these feeds. In Trial 2, seven dried distillers grains from different distilling plants were tested for N digestibility using 24 wethers (average BW 35 kg +/- 3.6). Visual differences in color indicated possible differences in degree of heating in these feeds. The ADIN contents were quite variable among these feeds; however, there were no differences in N digestibility. The correlation between ADIN and N digestibility was weak (r2 = .24). These results indicate that ADIN values in nonforage protein sources predicted more protein damage than that estimated by in vivo N digestibility values.

Three studies were conducted to evaluate N and amino acid (AA) availability from processed soybean (SB) products. In Exp. 1 and 2, treatments consisted of corn-cottonseed hull basal diets plus SB products including SB meal (SBM); ground, raw SB (RSB); or extruded SB (ESB). In Exp. 1, 15 Suffolk (28.6 kg) and 15 Louisiana native breed (16.3 kg) ewe lambs were used in a 35-d growth trial. Although breed affected (P < .10) DMI and ADG of lambs, the diets did not (P > .10). In Exp. 2, 12 Suffolk wether lambs (34.0 kg) were used in a 3 x 3 multiple-square Latin square design N metabolism trial. Lambs fed RSB tended (P = .13) to retain more N than those fed ESB, but N retained by lambs fed RSB and ESB was similar (P > .10) to that of lambs fed SBM. In Exp. 3, four crossbred steer calves (240 kg) were used in a 4 x 4 Latin square design N metabolism trial with the above treatments plus heat-damaged SB (HDSB). Calves fed RSB and ESB retained similar (P > .10) amounts of N. Compared with calves fed RSB and ESB, calves fed SBM retained more (P < .10) N. Calves fed HDSB retained less (P < .10) N than those fed other diets. The individual SB products and the total mixed diets used in Exp. 3 were incubated intraruminally in nylon bags and the residual DM recovered and precision-fed to cecectomized roosters to estimate its intestinal AA digestibility. Digestibility of residual AA seemed to be relatively uniform across AA.(ABSTRACT TRUNCATED AT 250 WORDS)