Examination of weekly mammary parenchymal area by ultrasound, mammary mass, and composition in Holstein heifers reared on 1 of 3 diets from birth to 2 months of age.

Monitoring in vivo growth of mammary parenchyma (PAR) has historically been difficult, necessitating slaughter studies to measure PAR quantity. Advances in ultrasound (US) technology warrant revisiting its use as a noninvasive tool to monitor PAR growth in vivo. The level of nutrient intake during the first 2mo of life may affect measures of mammary growth and composition. Objectives were to examine the utility of US as an in vivo tool to quantify PAR cross-sectional area in Holstein heifers reared on 1 of 3 diets from birth to 2mo of age, assessing potential dietary effects; assess the relationships between weekly US measurements, teat length, manual palpation of PAR scores, and PAR mass at 2mo of age; and examine mammary composition in experimental animals. Holstein heifers (n=24; 41±1kg of initial body weight) from a single farm were randomly assigned to 1 of 3 milk replacers that differed in source and amount of fat. Milk replacer was fed at 660g of dry matter/d until weaning at 42 d. Heifers had ad libitum access to a common calf starter (20% crude protein) and water for the duration of the 56-d trial. Teat length and palpation scores were obtained weekly. A real-time B-mode US with a 7.5-MHz convex probe was used to examine 2-dimensional PAR area in all 4 glands of heifers once weekly from 2 to 3 d of age to harvest at 56 d. The left front and left rear glands were also examined by US 24h postharvest to validate final US measurements, and then bisected to produce a sagittal plane view of PAR for comparison with US images. Mass and composition of mammary gland tissue were determined at 8 wk using standard methodology. Over the course of this 8-wk trial, average teat length increased from 11 to 17mm. The PAR area started small (6.6±3.2mm(2) per gland) and increased to 42.1±2.5mm(2) per gland by the end of the trial. As anticipated, based on measurements obtained at slaughter, US measurements were more related to amount of PAR (r=0.74) than either teat length (r=0.34) or palpation scoring (r=0.63). Importantly, US is quantitative, whereas palpation scoring is subjective. Diet did not affect mass or composition of PAR in young heifers; total udder PAR mass averaged 1.40±0.80g. In conclusion, we showed that in heifers younger than 2mo of age, obtaining weekly PAR measurements via ultrasound is an effective quantitative tool for measuring changes in PAR area in vivo. Future studies may incorporate and expand upon the methods developed here to determine what quantitative evaluation of PAR in young heifers can reveal about milk production capacity.

Lipid metabolism mRNA expression and cellularity of intramuscular adipocytes within the Longissimus muscle of Angus- and Wagyu-sired cattle fed for a similar days on feed or body weight endpoint.

This study investigates intramuscular (IM) adipocyte development in the Longissimus muscle (LM) between Wagyu- and Angus-sired steers compared at a similar age and days on feed (D) endpoint or similar body weight (B) endpoint by measuring IM adipocyte cell area and lipid metabolism mRNA expression. Angus-sired steers (AN, n = 6) were compared with steers from two different Wagyu sires (WA), selected for either growth (G) or marbling (M), to be compared at a similar days on feed (DOF; 258 ± 26.7 d; WA-GD, n = 5 and WA-MD, n = 5) in Exp. 1 or body weight (BW; 613 ± 18.0 kg; WA-GB, n = 4 and WA-MB, n = 5) in Exp. 2, respectively. In Exp. 1, WA-MD steers had a greater (P ≤ 0.01) percentage of IM fat in the LM compared with AN and WA-GD steers. In Exp. 2, WA-MB steers had a greater (P ≤ 0.01) percentage of IM fat in the LM compared with AN and WA-GB steers. The distribution of IM adipocyte area was unimodal at all biopsy collections, with IM adipocyte area becoming progressively larger as cattle age (P ≤ 0.01) and BW increased (P ≤ 0.01). Peroxisome proliferator activated receptor delta (PPARd) was upregulated earlier for WA-MD and WA-MB cattle compared with other steers at a similar DOF and BW (P ≤ 0.02; treatment × biopsy interaction). Peroxisome proliferator activated receptor gamma was upregulated (PPARg) at a lesser BW for WA-MB steers (P = 0.09; treatment × biopsy interaction), while WA-MD steers had a greater (P ≤ 0.04) overall mean PPARg mRNA expression compared with other steers. Glycerol-3-phosphate acyltransferase, lipin 1, and hormone sensitive lipase demonstrated mRNA expression patterns similar to PPARg and PPARd or CCAAT enhancer binding protein beta, which emphasizes their importance in marbling development and growth. Additionally, WA-MD and WA-MB steers often had a greater early mRNA expression of fatty acid transporters (fatty acid transport protein 1; P < 0.02; treatment × biopsy interaction) and binding proteins (fatty acid binding protein 4) compared with other steers. Cattle with a greater marbling propensity appear to upregulate adipogenesis at a younger chronological and physiological maturity through PPARd, PPARg, and possibly adipogenic regulating compounds, lysophosphatidic acid, and diacylglycerol. These genes and compounds could be used as potential markers for marbling propensity of cattle in the future.

This study investigates intramuscular (IM) adipocyte development in the Longissimus muscle (LM) between Wagyu- and Angus-sired steers compared at a similar age and days on feed (D) or similar body weight (B) endpoint by measuring IM adipocyte cell area and lipid metabolism mRNA expression. Angus-sired steers (AN) were compared with steers from two different Wagyu sires (WA), selected for either growth (G) or marbling (M), to be compared at a similar days on feed (DOF; WA-GD, and WA-MD) in Exp. 1 or body weight (BW; WA-GB, and WA-MB) in Exp. 2. The WA-MD and WA-MB steers had a greater percentage of IM fat in the LM compared with AN and WA-GD and WA-GB steers. Intramuscular adipocyte cellularity analysis indicated few differences due to adipocyte size; therefore, marbling differences were likely due to adipocyte number. The WA-MD and WA-MB steers typically experienced an earlier or a greater mRNA upregulation for adipogenic genes that regulate fatty acid transport and triglyceride synthesis compared with other steers. The pattern of mRNA expression was very similar between steers compared at either a similar age and DOF or BW. Indicating that the timing of energy intake above maintenance requirements may be more influential than age for the upregulation of lipid metabolism in cattle.

Forages and pastures symposium: forage biodegradation: advances in ruminal microbial ecology.

The rumen microbial ecosystem provides ruminants a selective advantage, the ability to utilize forages, allowing them to flourish worldwide in various environments. For many years, our understanding of the ruminal microbial ecosystem was limited to understanding the microbes (usually only laboratory-amenable bacteria) grown in pure culture, meaning that much of our understanding of ruminal function remained a "black box." However, the ruminal degradation of plant cell walls is performed by a consortium of bacteria, archaea, protozoa, and fungi that produces a wide variety of carbohydrate-active enzymes (CAZymes) that are responsible for the catabolism of cellulose, hemicellulose, and pectin. The past 15 years have seen the development and implementation of numerous next-generation sequencing (NGS) approaches (e.g., pyrosequencing, Illumina, and shotgun sequencing), which have contributed significantly to a greater level of insight regarding the microbial ecology of ruminants fed a variety of forages. There has also been an increase in the utilization of liquid chromatography and mass spectrometry that revolutionized transcriptomic approaches, and further improvements in the measurement of fermentation intermediates and end products have advanced with metabolomics. These advanced NGS techniques along with other analytic approaches, such as metaproteomics, have been utilized to elucidate the specific role of microbial CAZymes in forage degradation. Other methods have provided new insights into dynamic changes in the ruminal microbial population fed different diets and how these changes impact the assortment of products presented to the host animal. As more omics-based data has accumulated on forage-fed ruminants, the sequence of events that occur during fiber colonization by the microbial consortium has become more apparent, with fungal populations and fibrolytic bacterial populations working in conjunction, as well as expanding understanding of the individual microbial contributions to degradation of plant cell walls and polysaccharide components. In the future, the ability to predict microbial population and enzymatic activity and end products will be able to support the development of dynamic predictive models of rumen forage degradation and fermentation. Consequently, it is imperative to understand the rumen's microbial population better to improve fiber degradation in ruminants and, thus, stimulate more sustainable production systems.

Forage degradation in the rumen is critical to producing ruminant animals. For many years, scientists were limited to biochemical techniques to understand how ruminal microbes degraded forage, impairing our understanding of which microbes were involved with degrading which forage components. However, we have understood that as the ruminant opened up plant cells to microbial activity, a succession of microbes was involved in colonizing and breaking fiber into increasingly smaller pieces. The recent development of sequencing techniques has allowed a more detailed understanding of changes in the microbial population of the rumen during forage degradation and the types of degradative enzymes produced by this complex microbial ecosystem. We described the enzymes involved in the degradation of specific forage components, how their end products impact the microbial population through cross-feeding interactions, and how fermentation products can impact food animal production.

Use of trainer animals to improve performance and health of newly arrived feedlot calves.

Four trials were conducted to determine the efficacy of using trainer animals to improve the health and performance of newly arrived feedlot calves. For all trials, trainer animals were given 3 wk to adapt to the feedlot before arrival of the feeder calves and initiation of the trials. Trainer animals were present with newly received feedlot calves for 14 d after arrival and then were removed from the pens for the remaining 14 d of the experiments. In Trial 1, trainer animals were six crossbred beef steers and six mature cull beef cows. Newly received calves were allotted to 18 pens with 10 calves/pen. Six pens contained a trainer steer and six pens contained a trainer cow. Similar procedures were used for the subsequent three trials, except 12 trainer cows and 24 pens were used, and in Trial 4 half of the calves were allotted to pasture paddocks for 14 d before placement in their feedlot pens. During wk 1 of Trial 1, calves with trainer cows and steers gained weight more rapidly (P < .10) than those without a trainer animal (1.12 vs .67 kg/d, respectively). During wk 2, this trend was reversed and overall gains did not differ (P > .20) among treatment groups. Morbidity was 16.7 for control calves, 28.3% for calves with trainer steers, and 8.3% for calves with trainer cows. Four of six trainer steers required antibiotic treatment for respiratory disease. On d 1, a greater (P < .05) percentage of calves in the trainer cow group (81.7%) were observed eating during the first 30 min after feeding compared with either the steer trainer group (60%) or the control group containing no trainer animal (48.3%). This trend continued on d 2 but was not evident on d 3 or 7. In Trial 2, overall gains were 10% greater (P < .06) and final BW was higher (P < .01) for calves with trainer cows than for those without trainers. Trainer cows resulted in a substantial reduction (P < .01) in calf morbidity compared with calves housed alone. In Trial 3, trainer cows did not improve performance or health of newly received calves. More (P < .07) calves with trainers than without were eating 5 min after feeding on d 1, 2, 4, and 8. In Trial 4, the presence of trainer cows the first 2 wk did not affect (P > .27) gains. However, calves placed on pasture after arrival had lower (P < .03) gains during wk 1 than those housed in the feedlot. Calves placed in pasture paddocks upon arrival had more than twice (P < .01) the incidence of morbidity of those placed directly in the feedlot. In these trials, trainer cows had a significant effect on eating behavior of newly received calves, but health and performance benefits were variable.

Effects of concentration and source of supplemental fat and protein on performance of newly arrived feedlot steers.

Three experiments were conducted to determine the effects of supplemental fat and CP concentration in diets of newly received steers. In Exp. 1, 72 steers (initial BW 201 +/- 17 kg) were used in a 2 x 2 x 2 factorial experiment to determine effects of fat (Megalac, a calcium soap of palm fatty acids [CS]) concentration (0 vs 2%), CP concentration (12 vs 14%), and CP source (spray-dried blood meal [BM] vs soybean meal [SBM]) in receiving diets. Steers fed BM ate 22.8% more during wk 1 and 15.0% more during wk 2 if there was no CS in their diets compared with steers fed BM plus 2% CS (P < .05). In Exp. 2, 160 steers (initial BW 247 +/- 16 kg) were used in a randomized complete block design experiment to determine effects of adding CS (0, 2, or 4%) to 14% CP diets containing BM. No differences (P > .10) in ADG or feed efficiency (FE) occurred due to CS. In Exp. 3, 186 steers (initial BW 243 +/- 20 kg) were used in a randomized complete block design experiment to determine effects of supplemental fat source in receiving diets on steer performance. Diets contained either 0% added fat (control), 4% CS, or 4% animal-vegetable blend (AV). Feeding AV improved (P < .05) ADG and FE during wk 2 and FE for the total trial. Addition of AV to high-protein (15 to 22% CP) receiving diets improved FE, and CS resulted in no improvements in performance.

Effects of dietary energy intake and protein concentration on performance and visceral organ mass in lambs.

Eighty-eight early-weaned Hampshire x Targhee crossbred lambs (initial BW 23 +/- 3.9 kg) were used in a 2 x 2 factorial design experiment to determine the effects of DM and CP intake on lamb performance and weight and accretion rates of visceral organs during two periods of growth, divided at 36 kg live weight. There were 10 lambs per replicate and two replicate pens per treatment. Dry matter intake was 100 or 85% of ad libitum, and protein intake was 100 (normal) or 125% (high) of the calculated NRC (1985) requirement. Over both periods, lambs allowed ad libitum access to feed had greater (P < .05) ADG, rumen/reticulum, large intestine, and liver weights and faster accretion rates than lambs fed at 85% of ad libitum; however, there were no differences (P = .87) in feed efficiency. For the total trial, lambs fed high protein had greater (P < .01) DMI, ADG, liver and kidney weight and accretion rates, and increased (P < .01) feed efficiency during period 1 compared with lambs fed normal protein concentrations. Diets containing high concentrations of dietary protein resulted in greater DMI and ADG throughout the feeding period compared with diets formulated at NRC (1985) recommended concentrations, indicating that NRC (1985) protein recommendations may limit lamb performance. Restricted feeding resulted in reduced visceral organ mass compared with offering feed for ad libitum consumption. Restricted feeding increased efficiency of feed utilization for gain, in part, through reductions in visceral organ mass.

Effects of protein concentration and protein source on performance of newly arrived feedlot steers.

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.

Effects of corn processing, dietary roughage level, and timing of roughage inclusion on performance of feedlot steers.

In Trial 1, 108 crossbred steer calves (initial BW 295 kg) were allotted to 12 pens and used in a 186-d feedlot trial to determine the effects of increasing or decreasing roughage level on feedlot performance and carcass characteristics. Four dietary treatments were investigated: 1) 85% concentrate diet fed for 186 d, 2) 100% concentrate diet fed for 186 d, 3) 85% concentrate diet fed for 84 d followed by a 100% concentrate diet for the remaining 102 d, and 4) 100% concentrate diet for 84 d followed by an 85% concentrate diet for the remaining 102 d. Corn silage was added as roughage. During the first 84 d, level of dietary concentrate did not affect (P > .10) ADG. Steers switched to the 85% concentrate diet for the last 102 d had higher (P < .05) DMI than those fed the 100% concentrate diet; they did not exhibit an increase in ADG. Finishing phase feed efficiency was highest (P < .05) for steers continually fed 100% concentrate, lowest (P < .05) for steers continually fed 85% concentrate, and intermediate for steers whose concentrate level was switched during the trial. Carcass characteristics were not affected (P > .10) by concentrate level regimen. In Trial 2, 108 crossbred steer calves (initial BW 319 kg) were allotted to 12 pens and used in a 158-d trial to determine whether feedlot performance could be enhanced by manipulating roughage level and grain processing. Factors investigated were staged increases in concentrate level (70 to 85 to 100%) vs staged decreases in concentrate level (100 to 85 to 70%) and whole vs rolled high-moisture corn. Corn silage was added as roughage. Diet concentrate levels were changed on d 56 and 112. During the first 56 d, steers fed 70% concentrate diets grew 11% faster (P < .05) and consumed 19% more feed (P < .05) than those fed 100% concentrate diets. Steers fed rolled corn gained 8% faster (P < .06) and were 7% more efficient (P < .06) than those fed whole corn. During the last period (d 113 to 158), ADG was not affected (P > .10) by concentrate level or corn processing. Although increasing roughage during the feeding period increased feed intake in these trials, steer performance was not enhanced. Processing high-moisture corn did not affect feedlot performance.

Effects of programming intake on performance and carcass characteristics of feedlot cattle.

We conducted two experiments to determine the effects of various intake restriction strategies on performance and carcass characteristics of feedlot cattle. In Exp. 1, 104 steer calves (273 +/- 12 kg BW) were allotted to 12 pens. During Period 1 (273 to 372 kg BW), steers were limit-fed according to net energy equations to achieve predicted gains of .91, 1.13, or 1.36 kg/d. Control steers were offered ad libitum access to feed during this period. During Period 2 (372 to 535 kg BW), all steers were offered ad libitum access to feed. In Period 1, steers limit-fed for predicted gains of .91, 1.13, and 1.36 kg/d gained 1.03, 1.22, and 1.40 kg/d, respectively. Control steers offered ad libitum access to feed gained 1.66 kg/d. Steers that were limit-fed in Period 1 were able to compensate in Period 2; for the total experiment, there were no differences (P > .10) among the four feeding strategies investigated for rate of gain, feed efficiency, total feed intake, and carcass characteristics. Experiment 2 used 107 steer calves (300 +/- 11 kg BW). Four feeding strategies were compared: step-wise increases in intake to program for increasing rate of gain, stepwise decreases in intake to program for decreasing rate of gain, feeding to hold gain constant at 1.36 kg/d, or offering steers ad libitum access to feed throughout the experiment to allow for maximum gains. When averaged over the total experiment, growth rate and days on feed were not affected (P > .10) by feeding system. Steers fed to achieve a step-wise increase in growth rate throughout the experiment had the lowest (P < .09) daily intakes and the highest (P < .09) feed efficiencies. Steers fed for increasing gains required 109 kg/steer less (P < .09) total feed to reach market weight than those offered ad libitum access to feed throughout the experiment. Feeding strategy had little effect on carcass characteristics. We concluded that as intake is restricted to a greater extent, net energy equations are less accurate in predicting rate of gain. Programming intake during the feeding period can result in significant reductions in feed expenditures.

Effects of dietary energy source and level on performance of newly arrived feedlot calves.

Three experiments were conducted with Simmental x Angus crossbred steers to determine the effects of energy source and level on performance of newly arrived feedlot calves. In trial 1, 68 steers (initial BW 215 +/- 9.4 kg) were used in a 2 x 3 factorial experiment to determine the effects of receiving diet and previous creep feed on performance. Diets were composed primarily of either corn silage, corn silage + alfalfa pellets + dry corn, or dry corn + alfalfa pellets. For the 41-d trial, calves fed the corn silage-based diet had greater (P < .05) ADG and feed efficiencies than calves fed the other two diets. In Trial 2, 60 steers (initial BW 212 +/- 4.6 kg) were used in a 28-d completely randomized design experiment to determine the effects of 16% CP receiving diets containing 70, 75, 80 or 85% concentrate on performance. There were no differences (P > .10) in ADG or feed efficiency due to dietary concentrate level. In Trial 3, 77 steers (initial BW 226.3 +/- 3.0 kg) were used in a 2 x 3 factorial experiment to determine the effects of dietary concentrate and protein levels on performance during a 28-d receiving period. The factors were concentrate level (70 vs 85% concentrate) and protein level (12.5%, 16%, or phase-fed at 23%, 17%, 14%, and 12.5% during wk 1, 2, 3, and 4, respectively). During wk 1, calves fed the 85% concentrate diet had greater (P < .01) DMI, ADG, and feed efficiency compared with 70% concentrate. Calves fed the 16% CP and phase-fed protein diets had greater (P < .01) DMI, ADG, and greater (P < .02) feed efficiency than calves fed the 12.5% CP diets. Receiving diets containing at least 16% CP and > 70% concentrates are beneficial to calves during the first week after feedlot arrival.

Physiological changes and digestive capabilities of newly received feedlot cattle.

Newly arrived feedlot calves undergo numerous stressors that result in 1) transient endocrine responses, 2) altered products of energy and protein metabolism, 3) changes in appetite and growth rate, 4) possible limited compromise of digestive and rumen function, and 5) a challenged immune system. The most consistent endocrine and metabolic responses to marketing, transport, and feedlot adaptation are seen with cortisol and epinephrine. In contrast to earlier work done with indirect in vitro gas production measurements, recent research has shown that the ruminal microbial population is able to effectively digest available substrate immediately following a calfs weaning, trucking, and 24 h of feed and water deprivation. Additionally, a period of feed and water deprivation up to 72 h coupled with 8 h of trucking does not reduce the concentration or total numbers of either the viable cellulolytic or total bacteria present in the rumen of newly weaned or feedlot-adapted calves. However, ruminal volume, DM, total weight of ruminal contents, and total protozoal numbers decrease as duration of feed deprivation increases. To compensate for the reduced DMI that occurs in the first 2 wk after arrival at the feedlot, increased nutrient density is needed to meet an animal's requirements for nutrients. Limited data suggest that newly arrived calves prefer a diet that is similar in moisture and texture to feeds with which they are familiar. Additionally, modification of the stress-associated behavior using trainer animals may improve the feed intake of newly received calves and may reduce calf morbidity.

The influence of intake level and corn processing on digestibility and ruminal metabolism in steers fed all-concentrate diets.

The effects of intake (ad libitum and 70% of ad libitum) and corn processing (whole or rolled) on digestion, ruminal metabolism, and blood metabolites were determined in a 2 x 2 factorial experiment using eight ruminally fistulated steers. All-concentrate diets were fed with adjustments to dietary concentrations of N, vitamins, and minerals to ensure equal daily intake of these nutrients. Digestion of DM, OM, and starch were affected by an intake x processing interaction (P < .03). Starch digestion for the low-intake, whole-corn diet was much lower than that for the other three diets. This decrease in starch digestion was the major reason for the interaction. Nitrogen digestion was improved (P < .03) with limited intake but was not affected by processing. Ruminal volume and ruminal turnover (percentage/hour) were both reduced (P < .03) on the low-intake diet. Molar proportion of acetate was reduced and propionate was increased (P < .01) for steers receiving high intake of rolled corn compared with the other three diets. Butyrate concentrations were increased (P < .01) when corn was rolled before feeding. Ruminal pH was higher immediately before feeding for steers receiving whole corn than for those receiving rolled corn. Decreases in pH were observed for rolled corn 2 to 9 h after feeding, suggesting a faster rate of fermentation of rolled corn than of whole corn. Concentrations of blood glucose and insulin were not affected by intake or processing. It was concluded that processing corn can improve DM and OM digestibility if intake is restricted and that N digestion is improved with restricted feeding.(ABSTRACT TRUNCATED AT 250 WORDS)

Effects of energy density and protein source on diet digestibility and performance of calves after arrival at the feedlot.

Sixty Angus crossbred steers (initial BW, 237 kg) were used in a 2 x 2 factorial experiment to determine the effects of energy density and protein source in receiving diets on steers performance and total tract nutrient digestion. The factors compared were energy density (1.80 vs 1.48 Mcal/kg of NEm, referred to as high-energy and low-energy, respectively) and protein source (ring-dried blood meal [BM] vs soybean meal [SBM]). Diets containing BM resulted in a 10.6% greater (P < .09) ADG and a 7.6% improvement (P < .05) in efficiency of feed utilization compared with those containing SBM. High-energy diets resulted in an 8.7% improvement (P < .05) in feed efficiency vs low-energy diets. Dry matter digestibility (DMD), NDF digestibility (NDFD), and CP digestibility (CPD) were exceptionally high during wk 1, when DMI was approximately 1.5 kg/d. Nutrient digestibility declined during wk 2 and 3, as intake increased, before stabilizing between wk 4 and 6. Additionally, NDFD was not consistently lower (P > .10) during this study for high-energy diets than for low-energy diets. The results of the overall performance data indicate that, compared to SBM, feeding BM may improve ADG and feed efficiency during the receiving period when dietary CP is approximately 13%. Additionally, DMD, NDFD, and CPD were higher on d 7 than at any other time, indicating that by d 7 ruminal function was not adversely affected. Therefore, it seems that the reduced feed intake and growth rate normally seen during the first 2 wk in the feedlot is not caused by a reduction in diet digestibility.

Effects of programmed gain strategies on performance and carcass characteristics of steers.

In Trial 1, 161 Angus x Simmental crossbred steers (initial BW 305 +/- 1.0 kg) were used in a completely randomized design experiment to determine the effects of intake restriction and programmed gain on cattle performance and carcass composition and characteristics. Five feeding systems were tested using step-wise increases in programmed intake level. Initially steers were fed to gain 1.13 kg/d. Intake was then increased to achieve a gain of 1.36 kg/d. At the end of the feeding period, steers had ad libitum access to feed. Duration of intake restriction and the period of unrestricted intake was varied. Feeding steers at restricted intakes and then increasing daily gain by increasing feed intake using four different schedules all reduced (P < .05) daily feed intake and total feed intake compared with providing ad libitum access to feed throughout the trial. Furthermore, daily feed efficiency was increased (P < .05) by two of the feeding systems compared with offering ad libitum access to feed throughout the trial. The feeding system used did not affect (P > .10) quality grade of the carcasses. In Trial 2, 77 individually penned Angus x Simmental crossbred steers (initial BW 273 +/- 1.2 kg) were used to determine the effects of various feed intake restriction systems. For systems 1 through 4, multiple periods of restriction and realimentation were investigated; the duration and magnitude of restriction were varied. Feed intake was not restricted for steers in system 5. The feed restriction systems used in this experiment did not result in decreased total feed intake or changes in carcass composition as compared with offering ad libitum access to feed. Reducing total energy intake seems to be a prerequisite to altering feed efficiency of steers in limit-feeding systems.

Effect of source and amount of energy and rate of growth in the growing phase on adipocyte cellularity and lipogenic enzyme activity in the intramuscular and subcutaneous fat depots of Holstein steers.

Seventy-three Holstein steers (initial BW 138.5 +/- 4.3 kg; approximately 3 mo of age) were allotted by BW to one of three growing-phase treatments to determine the effect of source and amount of energy on feedlot performance, and characteristics of subcutaneous (s.c.) and intramuscular (i.m.) adipose tissue. Treatment diets were 1) high concentrate fed ad libitum (ALC); 2) high forage fed ad libitum for 55 d, then a mid-level forage diet fed ad libitum for 98 d (ALF); or 3) limit-fed high concentrate to achieve a gain of 0.8 kg/d for 55 d, then to achieve a gain of 1.2 kg/d for 98 d (LFC). All steers were fed the ALC diet from d 154 to slaughter. Eight steers per treatment were selected after an average of 145 and 334 d on feed for determination of adipocyte cellularity and lipogenic enzyme activity at the end of the growing and finishing phases, respectively. Remaining steers were slaughtered after an average of 334 d on feed. At initial slaughter, ALC steers had a two- to threefold greater (P < 0.05) s.c. fat depth, and 1.9-fold greater (P < 0.01) longissimus muscle ether extract than steers in other groups. At final slaughter, LFC steers had a greater fat depth than ALF steers (P < 0.10) and had the greatest (P < 0.10) longissimus muscle ether extract. Increased fat depth for ALC steers at initial slaughter was a result of a greater (P < 0.05) mean adipocyte diameter in the s.c. depot. Mean i.m. adipocyte diameter followed the same trend (P < 0.16). The number of adipocytes per gram of s.c. fat was least for ALC and greatest for ALF (P < 0.10) at initial slaughter. Mean diameter and number of adipocytes per gram of i.m. and s.c. fat did not differ among treatments at final slaughter (after 180 d on a common finishing diet). High energy (ALC) increased activities of ATP-citrate lyase, fatty acid synthase, 6-phosphogluconate dehydrogenase, glucose-6-phosphate dehydrogenase, and malate dehydrogenase (P < 0.05), in the s.c. depot, and increased activities of ATP-citrate lyase and glucose-6-phosphate dehydrogenase (P < 0.10) in the i.m. depot at initial slaughter. Lipogenic enzyme activity in the s.c. depot at final slaughter did not differ among treatments. Glucose-6-phosphate dehydrogenase activity in the i.m. depot at final slaughter was lowest (P < 0.10) in ALF. Hypertrophy made a greater contribution to fat tissue growth than hyperplasia. Hypertrophy was affected by amount of energy, whereas hyperplasia was affected by source of energy. Differences diminished when cattle were fed the common finishing diet.

Effects of crude protein concentration in diets of feedlot steers fed to achieve stepwise increases in rate of gain.

Two experiments were conducted to determine supplemental CP requirements for feedlot steers prescription-fed to achieve stepwise increases in ADG during the feeding period. In Exp. 1, 106 steers (initial BW = 285.7 +/- 3.4 kg) were allotted to 12 pens. Treatments consisted of ad libitum consumption of a 12% CP diet throughout the experiment (AL12%), prescription intake of a 12% CP diet (PI12%), or prescription intake of high-CP diets (PIHCP). The PIHCP diets were formulated to provide the same grams of CP per day as the AL12% diet. Steers in the prescription intake feeding regimens were fed to gain 1.13 kg/d for the first 87 kg of gain and 1.36 kg/d for the next 134 kg of gain and were offered feed for ad libitum consumption for the final 52 kg of gain before slaughter at 559 kg. Overall ADG was lower (P < 0.05) for steers fed PI12% and PIHCP diets than for those fed the AL12% diet (1.48 and 1.50 vs 1.60 kg/d, respectively). Total DM intake was lower (P < 0.08) for steers fed the PI12% and PIHCP diets than for steers fed the AL12% diet (1,359, 1,370, and 1,421 kg, respectively). Dressing percentage, back-fat thickness, and quality grade were lower (P < 0.05) for steers fed the PI12% and PIHCP diets than for steers fed the AL12% diet. In Exp. 2, 142 steers (initial BW = 285.4 +/- 3.1 kg) were allotted to 16 pens. System 1 was ad libitum consumption of a 12% CP diet throughout the experiment. Steers in Systems 2, 3, 4, and 5 were subjected to the same prescription intake strategy as steers in Exp. 1. During the three phases of growth (1.13 kg/d, 1.36 kg/d, and ad libitum), steers were fed the following CP concentrations: System 2(12, 14, and 12%); System 3(12, 14, and 14%); System 4(12, 16, and 12%); and System 5(12, 16, and 14%). No differences (P > 0.06) in total steer performance, carcass characteristics, or carcass chemical composition were observed among systems. Increasing percentage of CP in diets of prescription-fed steers to provide the same daily intake of CP as steers consuming feed ad libitum was not beneficial.

Ruminal characteristics, microbial populations, and digestive capabilities of newly weaned, stressed calves.

Eight ruminally fistulated steers, 7 to 8 mo old, were used in a completely randomized, 2 x 2 factorial experiment to determine the effects of energy density and protein source in receiving diets on in situ DM, NDF, and N disappearance, concentrations of ruminal bacteria, protozoa, ammonia, and pH. Two energy densities (1.80 and 1.48 Mcal/kg of NEm) and two protein sources (spray-dried blood meal [SDBM] and soybean meal [SBM]) were compared. Fistulated steers were weaned, transported by truck, and held in a sale barn before their arrival at the feedlot. On d 0 (day of arrival at the feedlot), DMI was 62% of DMI on d 7 after arrival. Overall, feeding a high-energy diet resulted in lower (P < .01) in situ DM disappearance (DMD) of orchardgrass than feeding a low-energy diet at both 24 and 48 h. In situ 24-h DMD averaged 46.6% on d-3 and 41.6% on d 0, whereas 48-h in situ DMD on d -3 and 0 averaged 58.2 and 58.6%, respectively, indicating the ruminal microbial population was not inhibited in its ability to digest available substrate. Additionally, there were no differences (P > .10) in 48-h in situ NDF disappearance between d -3 and 0 (58.8 vs 57.8%), respectively. No differences (P > .10) occurred in the concentration of total bacteria, or cellulolytic bacteria, due to feed and water deprivation. Concentration of total protozoa was lower (P < .05) on d 0 than at any other time. Entodinium averaged 72.5% of genera before weaning, and more than 90% of genera found on all treatments by d 21. Diplodinium and Epidinium percentages tended to decline after weaning. Isotricha concentrations were low and Dasytricha were eliminated after d 7. In conclusion, the concentration of ruminal bacteria and the ability to digest available substrate were not decreased immediately after weaning, trucking, and 24 h of feed and water deprivation.

Effects of feed and water deprivation on ruminal characteristics and microbial population of newly weaned and feedlot-adapted calves.

Two experiments were conducted to determine the effects of length of feed and water deprivation on ruminal microbes and ruminal characteristics. In Exp. 1, treatments were as follows: 1) weaned, but not trucked (0 h), 2) weaned, trucked, and fasted for 48 h (48 h), and 3) weaned, trucked, and fasted for 72 h (72 h). On d 0 (arrival back at the feedlot after treatment), DMI, ruminal contents (P < .05) decreased as length of feed and water deprivation increased. However, on d 4, there were no longer any differences (P > .10) in DMI or weight of ruminal contents. On d 0, percentage of ruminal DM in the 48- and 72-h treatment groups was lower (P < .01) than in the 0-h treatment group, but there were no differences (P > .10) by d 4. After the steers used in Exp. 1 had been in the feedlot for 28 h, they were reallotted, and the three treatments (except for weaning) were repeated; the 0-h group remained at the feedlot. On d 0, DMI of the 48-h group was lower (P < .05) than that of the 0-h group; DMI of the 72-h group was intermediate. On d 0, the 0-h treatment group had a greater ruminal DM percentage than the 48- and 72-h treatment groups (P < .05); however, due to large within-treatment variation the total weight of ruminal contents did not differ (P > .10) among treatments. There were no decreases (P > .10) in cellulolytic or total bacterial concentration or in the ruminal numbers of cellulolytic or total bacteria due to length of feed and water deprivation on d 0 in either Exp. 1 or 2. In both trials, 48 and 72 h of feed and water deprivation decreased (P < .05) protozoal numbers on d 0 and 4 compared with the 0-h treatment group.

Effects of supplemental protein source and alkaline hydrogen peroxide treatment of wheat straw on site of nutrient digestion and flow of nitrogenous compounds to the duodenum of steers.

The objective of this study was to determine the effects of soybean meal (SBM) or spray-dried blood meal (BM) supplementation of diets based on untreated (UNT-WS) or alkaline hydrogen peroxide-treated wheat straw (AHP-WS). A 4 x 4 Latin square design with a 2 x 2 factorial arrangement of treatments was used. Variables included nutrient digestion and flow to the duodenum. Four Simmental steers (average weight 477 kg) fitted with ruminal and duodenal cannulas were fed 65% UNT-WS or AHP-WS based diets in 12 equal portions daily. Diets were formulated to contain 10% CP. Chromic oxide was used as the digesta flow marker and purines were used as the microbial marker. There were no straw type x protein source interactions. Total tract and ruminal OM digestibility were approximately 25% greater (P < .04) when AHP-WS was fed than when UNT-WS was fed. Source of protein did not affect (P > .10) OM or fiber digestion in the rumen or total tract. Ruminal digestion of NDF and ADF was increased (P < .01) by 51 and 40%, respectively, when AHP-WS was fed than when UNT-WS was fed. Main effect means (P > .10) for N flow to the duodenum as a percentage of N intake were 128.2, 142.5, 133.4, and 137.6 for UNT-WS, AHP-WS, SBM, and BM treatments, respectively. Despite increased (P < .01) ruminal OM digestion for AHP-WS, microbial N flow to the duodenum was greater (P < .01) when UNT-WS was fed than when APH-WS was fed.(ABSTRACT TRUNCATED AT 250 WORDS)

Effects of calcium soaps of long-chain fatty acids on feedlot performance, carcass characteristics and ruminal metabolism of steers.

Two trials were conducted to determine the effects of calcium soaps of long-chain fatty acids (calcium soap) on feedlot performance, diet digestibility, carcass characteristics and ruminal metabolism of steers fed diets (85% concentrate:15% corn silage) containing 0, 2, 4 or 6% calcium soap. In Trial 1, increasing calcium soap decreased (P less than .05) DM, CP and gross energy intake but increased total fatty acid intake. Feed to gain ratio tended to improve with increased calcium soap; gross energy conversion was not affected (P greater than .05) by diet. Average daily gain and hot carcass weight decreased (P less than .05) with addition of calcium soap; other carcass characteristics were not affected (P greater than .05). Apparent digestibilities of DM, N, energy and ash were not affected (P greater than .05) by calcium soap. Neutral detergent fiber digestibility increased linearly (P less than .08) with increasing calcium soap, whereas digestibility of total fatty acids was affected quadratically (P less than .05); fatty acid digestibility was similar among 0, 2 and 4% calcium soap diets but decreased for the 6% calcium soap diet. In Trial 2, increased calcium soap did not affect (P greater than .05) ruminal VFA concentrations, pH or in sacco NDF disappearance of orchardgrass following 12, 24 and 48 h of incubation. Calcium soap increased (P less than .07) ruminal concentrations of calcium soap fatty acids at 1, 2, 4 and 8 h postfeeding. Calcium soap did not improve performance of feedlot cattle fed high-concentrate diets. Further, calcium soap did not affect ruminal fermentation and did not dissociate significantly even when ruminal pH was below 6 for extended periods of time.