Evaluation of wheat-based thin stillage as a water source for growing and finishing beef cattle.

Two trials were conducted to evaluate the nutritional value of wheat-based thin stillage as a water source for cattle. In Trial 1, 20 large-framed steers were fed a basal diet based primarily on barley grain and barley silage, with ad libitum access to water or thin stillage at one of three DM concentrations (2, 4, and 6.7%) in a completely randomized design. The trial consisted of a 70-d growing period and a finishing phase. In Trial 2, total-tract nutrient digestibility coefficients of the basal diet and water treatments fed in the growing period were determined in a randomized complete block design using 12 medium-framed steers. The results showed that when only DMI from the basal diet was considered, there was a linear reduction (P<.01) in DMI and a linear improvement (P<.01) in the gain:feed ratio with no effect on daily gain as thin stillage DM concentration increased. No differences were detected in DMI or efficiency of gain when total DMI (basal diet and thin stillage) was considered. Carcass traits indicated a trend toward increased (P<.06) carcass fat with increasing thin stillage DM concentration. Results of Trial 2 indicated a linear improvement (P<.05) in apparent digestibility of DM, CP, NDF, and energy of the total diet (basal diet and thin stillage) as thin stillage DM concentration increased. We concluded that supplementing growing and finishing cattle with thin stillage reduced the amount of the basal diet required for gain and improved nutrient utilization.     

Influence of supplemental nitrogen source on digestion of nitrogen, dry matter and organic matter and on in vivo rate of ruminal protein degradation

Seven Holstein steers (340 kg) fitted with ruminal, duodenal and ileal cannulae were used to measure the influence of supplemental N source on digestion of dietary crude protein (CP) and on ruminal rates of protein degradation. Diets used were corn-based (isonitrogenous, 12% CP on a dry matter basis, and isocaloric, 80% total digestible nutrients) with urea, soybean meal (SBM), linseed meal (LSM) or corn gluten meal (CGM) as supplemental N. Ruminal ammonia N concentrations were higher (P less than .05) in steers fed LSM than in those fed CGM, but did not differ from those in steers fed urea or SBM (11.7, 6.7, 9.1 and 9.2 mg/100 ml, respectively). Due to the high degradability of urea, ruminal digestion of dietary CP was greater (P less than .05) in steers fed urea than in those fed CGM, but intermediate in steers fed SBM and LSM (58.4, 48.8, 53.1 and 53.9%, respectively). Flow of bacterial nonammonia N to the duodenum was highest (P less than .05) in steers fed SBM or LSM, intermediate (P less than .05) for urea and lowest (P less than .05) for CGM (86.8, 86.1, 76.3 and 65.9 g/d, respectively). Efficiency of bacterial protein synthesis was lowest in steers fed CGM and differed (P less than .05) from SBM (15.6 vs 21.8 g N/kg organic matter truly digested, respectively). Rate of ruminal digestion for SBM-CP differed (P less than .05) from that of CGM-CP but not from that of LSM-CP (17.70, 5.20 and 10.13%/h, respectively). The slow rate of ruminal degradability of CGM resulted in increased amounts of dietary protein reaching the intestinal tract but lower amounts of bacterial protein, thus intestinal protein supply was not appreciably altered.     

Effects of dietary protein levels and 2‐methylbutyrate on ruminal fermentation,nutrient degradability,bacterial populations and urinary purine derivatives in Simmental steers

The objective of this study was to evaluate the effects of dietary crude protein (CP ) levels and 2‐methylbutyrate (MB ) supplementation on ruminal fermentation, bacterial populations, microbial enzyme activity and urinary excretion of purine derivatives (PD ) in Simmental steers. Eight ruminally cannulated Simmental steers, averaging 18 months of age and 465 ± 8.6 kg of body weight (BW ), were used in a replicated 4 × 4 Latin square design by a 2 × 2 factorial arrangement. Low protein (98.5 g CP /kg dry matter [LP ] or high protein (128.7 g CP /kg dry matter [HP ]) diets were fed with MB supplementation (0 g [MB ?] or 16.8 g steer^?1 day^?1 [MB +]). Steers were fed a total mixed ration with dietary corn straw to concentrate ratio of 50:50 (dry matter [DM ] basis). The CP  × MB interaction was observed for ruminal total VFA , molar proportions of acetate and propionate, acetate to propionate ratio, ammonia‐N, effective degradability of neutral detergent fibre (NDF ) and CP , microbial enzyme activity, bacterial populations and total PD excretion (p  < .05). Ruminal pH decreased (p  < .05), but ruminal total VFA concentration increased (p  < .05) with increasing dietary CP level or MB supplementation. Acetate molar proportion increased (p  = .043) with MB supplementation, but was not affected by dietary CP level. Propionate molar proportion decreased (p  < .05) with increasing dietary CP level or MB supplementation. Consequently, acetate‐to‐propionate ratio increased (p  = .001) with MB supplementation, but was not affected by dietary CP level. Ruminal ammonia‐N content increased (p  = .034) with increasing dietary CP level, but decreased (p  = .012) with MB supplementation. The effective degradability of NDF and CP increased (p  < .05) with increasing dietary CP level or MB supplementation. Microbial enzyme activity, bacterial populations and total PD excretion also increased (p  < .05) with increasing dietary CP level or MB supplementation. The results indicated that ruminal fermentation, nutrient degradability, microbial enzyme activity, ruminal bacterial populations and microbial protein synthesis improved with increasing dietary CP level or MB supplementation in steers.     

Influence of supplemental protein source and protein concentration on ruminal and intestinal digestion in heifers

Six pregnant Holstein heifers fitted with ruminal cannulas and T-type duodenal cannulas were used in a 6 x 6 latin square design experiment to determine whether diets formulated on a rumen undegraded CP (UDP) equivalent basis would provide a more accurate estimate of protein quality for ruminants. Six diets (barley [B]/brome-alfalfa hay-based) were formulated to contain three concentrations of CP (14.0%, 16.5% and 19.0%) and three protein sources (canola meal [CM], meat and bone meal [MBM] and soybean meal [SBM]). The six diets were B, 14% CP, CM, 16.5% CP; SBM, 16.5% CP; MBM, 16.5% CP; CM, 19% CP; and SBM, 19% CP. The diets were formulated so that the 16.5% CP diets were equivalent on a CP basis, whereas the MBM16.5, CM19 and SBM19 were equivalent on a UDP basis. Diets were compared with regard to protein degradability in the rumen and protein flow to, and digestion in, the intestine. Animals fed the CM and SBM diets had higher (P less than .05) ruminal levels of branched-chain VFA than the control diet. Ruminal ammonia nitrogen (N) concentrations were affected (P less than .05) by supplemental protein source and concentration (8.8, 10.9, 11.2, 11.2, 13.2 and 17.7 mM for B14, CM16.5, SBM16.5, MBM16.5, CM19 and SBM19, respectively). Ruminal OM digestion was affected (P less than .05) by protein source MBM16.5, which was lower than protein source in all other diets. Total N flow to the small intestine for the three diets formulated on a UDP equivalent basis was 224.0, 225.6 and 241.1 g N/d for MBM16.5, CM19 and SBM19, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)     

Effects of canola seed supplementation on intake, digestion, duodenal protein supply, and microbial efficiency in steers fed forage-based diets

Fourteen Holstein steers (446 +/- 4.4 kg of initial BW) with ruminal, duodenal, and ileal cannulas were used in a completely randomized design to evaluate effects of whole or ground canola seed (23.3% CP and 39.6% ether extract; DM basis) on intake, digestion, duodenal protein supply, and microbial efficiency in steers fed low-quality hay. Our hypothesis was that processing would be necessary to optimize canola use in diets based on low-quality forage. The basal diet consisted of ad libitum access to switchgrass hay (5.8% CP; DM basis) offered at 0700 daily. Treatments consisted of hay only (control), hay plus whole canola (8% of dietary DM), or hay plus ground canola (8% of dietary DM). Supplemental canola was provided based on the hay intake of the previous day. Steers were adapted to diets for 14 d followed by a 7-d collection period. Total DMI, OM intake, and OM digestibility were not affected (P > or = 0.31) by treatment. Similarly, no differences (P > or = 0.62) were observed for NDF or ADF total tract digestion. Bacterial OM at the duodenum increased (P = 0.01) with canola-containing diets compared with the control diet and increased (P = 0.08) in steers consuming ground canola compared with whole canola. Apparent and true ruminal CP digestibilities were increased (P = 0.01) with canola supplementation compared with the control diet. Canola supplementation decreased ruminal pH (P = 0.03) compared with the control diet. The molar proportion of acetate in the rumen tended (P = 0.10) to decrease with canola supplementation. The molar proportion of acetate in ruminal fluid decreased (P = 0.01), and the proportion of propionate increased (P = 0.01), with ground canola compared with whole canola. In situ disappearance rate of hay DM, NDF, and ADF were not altered by treatment (P > or = 0.32). In situ disappearance rate of canola DM, NDF, and ADF increased (P = 0.01) for ground canola compared with whole canola. Similarly, ground canola had greater (P = 0.01) soluble CP fraction and CP disappearance rate compared with whole canola. No treatment effects were observed for ruminal fill, fluid dilution rate, or microbial efficiency (P > or = 0.60). The results suggest that canola processing enhanced in situ degradation but had minimal effects on ruminal or total tract digestibility in low-quality, forage-based diets.     

Influence of fish meal and supplemental fat on performance of finishing steers exposed to moderate or high ambient temperatures.

Ninety-six Hereford x Angus steers (mean initial BW = 295 kg) were used in two growth experiments conducted at moderate and high ambient temperatures (AT), 48 steers per AT. Within each AT, calves were assigned to six dietary treatments consisting of a basal diet (approximately 60% corn and 20% grass hay) supplemented with either 0, 2.5, or 5% fat and with either soybean meal (SBM) or Menhaden fish meal (FM) included at levels such that a ratio of 16.3 kcal of NEm per kilogram of CP was maintained. Blood and ruminal fluid were collected 40 d before slaughter. During the final 28 d of the moderate AT experiment, apparent digestibility of dietary components was measured in four individually fed steers from each dietary treatment. Steer ADG was not affected by fat, and DMI and efficiency of gain were not affected (P > .10) by treatment. Average daily gain was lower for steers fed FM than for those fed SBM at moderate AT but higher at high AT (CP source x AT interaction; P < .05). Ruminal ratio of acetate to propionate declined linearly with increasing fat at moderate AT but was not affected by fat at high AT (fat x AT interaction trend; P = .08). Plasma urea N concentration increased linearly (P < .05) with increasing fat and was higher (P < .05) in steers kept at high than in those kept at moderate AT. Although apparent digestibility was not altered in steers fed FM, DM and NDF (P < .05) and ADF (P = .07) digestibility decreased with increasing fat in steers fed SBM (CP source x fat interaction).(ABSTRACT TRUNCATED AT 250 WORDS)     

Daily and alternate-day supplementation of urea or biuret to ruminants consuming low-quality forage: III. Effects on ruminal fermentation characteristics in steers

Five ruminally and duodenally cannulated steers (491 +/- 21 kg BW) were used in an incomplete 5 x 4 Latin square with four 24-d periods to determine the influence of supplemental nonprotein N (NPN) source and supplementation frequency (SF) on the dynamics of ruminal fermentation in steers consuming low-quality grass straw (4% CP). Treatments (TRT) included an unsupplemented control (CON) and a urea or biuret supplement that were placed directly into the rumen at 0700 daily (D) or every other day (2D). The NPN treatments were formulated to provide 90% of the estimated degradable intake protein requirement; therefore, the urea and biuret treatments received the same amount of supplemental N over a 2-d period. Daily TRT were supplemented with CP at 0.04% of BW/d, whereas the 2D TRT were supplemented at 0.08% of BW every other day. Forage was provided at 120% of the previous 5-d average intake in two equal portions at 0715 and 1900. Ruminal fluid was collected 0, 3, 6, 9, 12, and 24 h after supplementation on a day of and a day before supplementation for all TRT. Ruminal NH3-N increased (P < 0.04) with CP supplementation on the day all supplements were provided and on the day on which only daily supplements were provided compared with the CON. However, an NPN source x SF interaction (P = 0.03) on the day all supplements were provided indicated that NH3-N increased at a greater rate for urea as SF decreased compared with biuret. Ruminal NH3-N on the day only daily supplements were provided was greater (P = 0.02) for D compared with 2D. On the day all supplements were provided, D increased (P = 0.05) ruminal indigestible acid detergent fiber passage rate and ruminal fluid volume compared with 2D. These results suggest that urea or biuret can be used effectively as a supplemental N source by steers consuming low-quality forage without adversely affecting ruminal fermentation, even when provided every other day.     

Effects of protein concentration and source on nutrient digestibility by mature steers limit-fed high-concentrate diets.

Five ruminally fistulated 3-yr-old mature Holstein steers (average BW 691+/-23 kg) were used in a 5 x 5 Latin square experiment with a 2 x 2 + 1 fact orial arrangement of treatments. Effects of protein concentration and protein source on nutrient digestibility, excretion of DM and fecal N, ruminal fluid volume and dilution rate, ruminal characteristics, and in situ DM disappearance of whole shelled corn, ground corn, and orchardgrass hay were measured in steers limit-fed high-concentrate diets at 1.5% of BW. A negative control basal diet (NC; 9% CP) was supplemented to achieve either 11 or 14% CP; supplemental CP was either from soybean meal (11 and 14% SBM) or a 50:50 ratio of CP from urea and soybean meal (11 and 14% U). Dry matter and OM digestibilities were 5% greater (P < .07) for steers fed the SBM diets than for those fed the U diets. Starch digestibility did not differ (P > .10) among steers fed any of the diets. Nitrogen source did not affect (P > .10) apparent N digestibility or fecal N excretion; however, steers fed the NC diet had the lowest (P < .10) apparent N digestibility compared with those fed all other diets. Ruminal fluid volume was lower (P < .06) when steers were fed the NC diet compared with all other diets; there were no differences (P > .74) among diets for ruminal fluid dilution rate. In general, ruminal ammonia N and VFA molar proportions were not affected by protein source or concentration. Although CP concentration affected (P < .06) in situ DM disappearance of ground corn, CP concentration did not (P > .48) affect total tract digestion of DM or OM. This indicates that CP concentration may have affected site of digestion, but not extent of digestion. When mature ruminants were limit-fed a corn-based diet to meet primarily a maintenance function, protein source and concentration had little effect on measures of nutrient digestion.     

Pretanned leather shavings in a supplement mixture for steers: I. In situ and in vitro disappearance, ruminal fermentation, and organic matter, nitrogen, and fiber digestion

Two digestion studies were conducted to evaluate the use of pretanned leather shavings as a component of a protein supplement. In Exp. 1, the in situ and in vitro disappearance of pretanned leather shavings and soybean meal was evaluated. Results revealed that less than 18.4% of the pretanned leather shavings was solubilized and disappeared when exposed to McDougall's buffer for 48 h, but there was 90.0% disappearance with 48-h exposure to a .1 N HCl/pepsin treatment and 97.0% disappearance with exposure to a two-stage digestion. In situ disappearance following 72 h in the rumen allowed 6.8% disappearance. Thus, leather shavings seem to be relatively indigestible in the rumen, but postruminal digestion may be possible. In Exp. 2, six Angus x Holstein steers, fitted with ruminal and duodenal cannulas, were used in a replicated 3 x 3 Latin square to evaluate ruminal and digestion effects of the following supplements combined with fescue hay at 1.7% of BW (DM basis): no supplementation (control); supplementation intraruminally with soybean meal at .07% of BW (as-fed basis); and supplementation intraruminally with a combination of soybean meal and pretanned leather shavings (17:8 ratio) at .05% of BW (isonitrogenous to soybean meal; as-fed basis). Ruminal fluid passage rate was greater and fluid turnover time was shorter in steers fed leather shavings than in those fed soybean meal (P = .10). Ruminal pH was lower (P = .04) for supplemented steers than for control steers and ruminal NH3 N concentration was greater (P = .01) in steers fed soybean meal than in those fed leather shavings. Total VFA concentration was increased (P = .02) by supplementation. Supplementation with soybean meal increased (P < .05) ruminal molar proportions of butyrate, valerate, and isovalerate compared with leather shavings. Duodenal OM flow and OM disappearing in the intestines were increased by supplementation (P < .10), but not by the type of supplement fed (P > .10). Ruminal digestion of OM and total tract OM digestion were unaffected (P > .10) by supplementation and the type of supplement fed. Flow and digestion of NDF were unaffected (P > .10) by the treatments. Flow of N and the quantity of N disappearing in the intestines were increased (P < .05) by supplementation but did not differ (P > .10) between supplementation groups. Microbial N flow, N utilization for net microbial protein synthesis, and ruminal N disappearance were unaffected (P > .10) by supplementation and the type of supplement provided. Combining pretanned leather shavings with soybean meal seemed to have no deleterious effects on digestion or fermentation and to allow for escape of some N to the lower tract.     

Influence of rumen protein degradability and supplementation frequency on steers consuming low-quality forage: II. Ruminal fermentation characteristics

Seven ruminally and duodenally cannulated steers (264 +/- 8 kg BW) consuming low-quality forage (5% CP; 61% NDF; 31% ADF) were used to determine the influence of CP degradability and supplementation frequency (SF) on ruminal fermentation characteristics. Treatments included an unsupplemented control and degradable intake protein (DIP) or undegradable intake protein (UIP) provided daily, every 3 d, or every 6 d. The DIP treatments (18% UIP) were calculated to provide 100% of the DIP requirement, while the UIP treatments (60% UIP) were provided on an isonitrogenous basis compared with DIP. Ruminal NH3-N was increased on the day all supplements were provided with supplemental CP (P = 0.04) and for DIP compared with UIP (P < 0.01). Also, because ruminal NH3-N increased at a greater rate with DIP compared with UIP as SF decreased, a linear effect of SF x CP degradability interaction (P = 0.02) was observed. In addition, NH3-N was greater on the day only daily supplements were provided for supplemented treatments (P = 0.04), and decreased linearly (P < 0.01) as SF decreased. Concentration of total VFA increased linearly (P = 0.02) as SF decreased on the day all supplements were provided, whereas on the day only daily supplements were provided, total VFA were greater for UIP compared with DIP (P = 0.01), and decreased linearly (P < 0.01) as SF decreased. An interaction concerning the linear effect of SF and CP degradability (P = 0.02) was observed for ruminal liquid volume on the day all supplements were provided. This was the result of an increase in liquid volume with DIP as SF decreased compared with a minimal effect with UIP. In contrast, there was no influence of supplementation on liquid volume the day only daily supplements were provided. Ruminal liquid dilution rate was greater (P = 0.02) with CP supplementation on the day all supplements were provided. We did observe a quadratic effect of SF x CP degradability interaction (P = 0.01) for dilution rate because of a quadratic response with DIP (greatest value with the every-third-day treatment) compared with a decrease as SF decreased for UIP. On the day only daily supplements were provided, ruminal liquid dilution rate decreased linearly (P = 0.02) as SF decreased. These results suggest that DIP and UIP elicit different effects on ruminal fermentation when supplemented infrequently to ruminants consuming low-quality forage while not adversely affecting nutrient intake and digestibility.     

Effects of cottonseed meal supplementation time on ruminal fermentation and forage intake by Holstein steers fed fescue hay.

Four ruminally cannulated Holstein steers (average BW 303 kg) were used in a 4 x 4 Latin square design digestion trial to study the influence of daily cottonseed meal (CSM; 1.6 g of CP/kg of BW) supplementation time on forage intake and ruminal fluid kinetics and fermentation. Steers were housed individually in tie stalls and were fed chopped fescue hay on an ad libitum basis at 0600 and 1400. Treatments were 1) control, grass hay only (CON) and grass hay and CSM fed once daily at 2) 0600 (EAM) 3) 1000 (MAM), or 4) 1400 (PM). Ruminal NH3 N concentrations reflected a time of supplementation x sampling time interaction (P less than .05); CON steers had the lowest (P less than .05) ruminal NH3 N concentrations at all times other than at 0600, 1000, 1200, and 2400, when they did not differ (P greater than .05) from at least one of the supplemented groups. Forage intake, ratio of bacterial purine:N, rate of DM and NDF disappearance, and ruminal fluid kinetics were not influenced (P greater than .05) by supplementation time. Total ruminal VFA differed (P less than .05) between CON and supplemented steers, as well as among supplemented steers (linear and quadratic effects P less than .05). Acetate, propionate, and valerate proportions were influenced (P less than .05) by a sampling time X supplementation time interaction. Under the conditions of this study, greater peak ammonia concentrations with morning supplementation than with afternoon supplementation did not stimulate ruminal fermentation or rate of NDF disappearance.     

Efficacy of laidlomycin propionate in low-protein diets fed to growing beef steers: effects on steer performance and ruminal nitrogen metabolism

We conducted two experiments to evaluate the effect of the ionophore laidlomycin propionate (LP) on steer performance and ruminal N metabolism. Experiment 1 was a 91-d growth study evaluating the growth and ruminal characteristics of steer calves consuming supplemental LP. Steers (n = 96; 255 +/- 3 kg; four steers/pen; six pens/treatment) were used in a randomized complete block design with a 2 x 2 factorial arrangement of treatments consisting of two levels of dietary CP (formulated to be 10.5 and 12.5% of DM) with and without LP (11 mg/kg diet DM). Ruminal fluid was collected via stomach tube on d 91 from one steer randomly selected from each pen. No CP x LP interactions were observed with performance data (P > .64). Final weight and total gain were greater (P < .07) for 12.5% CP and LP compared with 10.5% CP and control steers, respectively. Also, DMI was increased (P = .08) with 12.5% CP but not with LP supplementation (P = .36). In addition, ADG and gain:feed ratio were greater (P < .03) for both 12.5% CP and supplemental LP. Ruminal NH3 N concentration was greater (P < .09) with 12.5% CP and LP. Total VFA concentration and molar proportion of acetate were not affected by treatment (P > .11). However, propionate concentration was increased (P < .09) with 12.5% CP and LP, and acetate:propionate was lower (P = .02) with LP supplementation. In Exp. 2, six steers were used in a replicated 3 x 3 Latin square design to compare ruminal fermentation and protein degradation in steers without ionophore feeding or adapted to LP or monensin. In vitro deamination of amino acids by adapted ruminal microbes was also assessed. Ionophore supplementation decreased (P = .07) ruminal NH3 N concentration compared with control steers, and LP increased (P = .02) ruminal NH3 N compared with monensin. Molar proportion of acetate was decreased (P = .02) and propionate increased (P = .01) with ionophore treatment. Consequently, ionophore supplementation depressed the acetate:propionate ratio (P = .01). In situ degradation rate of soybean meal (SBM) CP was greater (P = .09) with ionophore treatment, but estimates of SBM undegradable intake protein were not altered by treatment (P > .25). Microbial specific activity of net NH3 N release and alpha-amino N degradation were decreased (P < .04) with ionophores. Based on this study, LP and monensin did not affect the extent of ruminal degradation of SBM CP but decreased amino acid deamination.     

Intraruminal supplementation with increasing levels of exogenous polysaccharide-degrading enzymes: effects on nutrient digestion in cattle fed a barley grain diet

The effects of supplying increasing ruminal doses of exogenous polysaccharide-degrading enzymes (EPDE) on rumen fermentation and nutrient digestion were studied using eight ruminally cannulated heifers, four of which were also duodenally cannulated, in a replicated Latin square. The heifers were fed a diet of 85.5% rolled barley grain and 14% barley silage (DM basis), and once daily they were given intraruminal doses of 0 (Control), 100, 200, or 400 g of a preparation containing polysaccharide-degrading enzymes. Enzyme treatment decreased ruminal pH (linear, P<.001) and increased ammonia N (quadratic, P<.001) concentration. The ruminally soluble fraction and effective degradability of feed DM in situ were increased (quadratic response, P<.001) by enzyme treatment. Ruminal administration of EPDE increased ruminal fluid carboxymethylcellulase and xylanase activities linearly (P<.001) and beta-glucanase activity quadratically (P<.01), decreased (quadratic response, P<.05) ruminal fluid viscosity, and did not affect (P>.05) ruminal fluid amylase activity. Elevated levels of fibrolytic activities in the rumen resulted in increased (quadratic, P<.001) carboxymethylcellulase, xylanase, and beta-glucanase (P<.01) activities in duodenal digesta. Duodenal amylase activity and reducing sugar concentration were also increased (quadratic responses, P<.001 and P<.05, respectively) by EPDE. Xylanase activity of fecal DM was increased linearly (P<.05) with increasing ruminal EPDE levels. Apparent digestibilities of DM, crude protein, and NDF were not affected by EPDE supplementation. Enzyme treatment did not affect (P>.05) urinary excretion of allantoin and uric acid, or concentrations of glucose and urea in blood.     

Dietary protein level and ruminal degradability for mohair production in Angora goats.

Twenty-eight Angora goat doelings (average BW 22.1 kg) were used in a 150-d study to examine the effects of dietary CP level and degradability on mohair fiber production. A 2 x 2 factorial arrangement was instituted using conventional, solvent-extracted soybean meal (high degradability) or expelled, heat-treated soybean meal (low degradability) incorporated into low- (12%) or high- (19%) CP diets. Grease and clean mohair weights were greater (P less than .05) in goats fed the diets containing 19% CP. Mohair fiber diameter was not affected (P greater than .10) by dietary CP level. Clean mohair weight tended (P less than .08) to be higher in the goats fed diets containing expelled, heat-treated soybean meal. Body weight gains were not affected (P greater than .10) by CP level or degradability, whereas DMI increased (P less than .01) with increasing CP level. Ruminal fluid pH and total VFA concentrations were not affected (P greater than .10) by diet. Ruminal ammonia N concentration increased (P less than .05) as CP level in the diet increased, and postprandial changes in concentrations were less noticeable in the group fed expelled, heat-treated soybean meal. Plasma urea N (P less than .001) and total protein (P less than .01) concentration increased as dietary CP level increased. Plasma glucose was elevated (P less than .001) 2 h after feeding in the goats fed conventional, solvent-extracted soybean meal, whereas glucagon concentrations were greater at 0 and 4 h in the group fed expelled, heat-treated soybean meal.(ABSTRACT TRUNCATED AT 250 WORDS)     

Effects of laidlomycin propionate and monensin on the in vitro mixed ruminal microorganism fermentation.

The objective of this study was to compare the effects of laidlomycin propionate and monensin on the in vitro fermentation of ground corn, Trypticase, or alfalfa hay by mixed ruminal microorganisms. Ruminal fluid was collected from two steers fed 9.27 kg DM of a high-concentrate (62.2% ground corn and 17.4% cottonseed hulls) diet per day and composited. In the first study, no ionophore was included in the diet; the diet in the second study contained 11.1 g of laidlomycin propionate per ton of feed. The animals were allowed an adjustment period of 14 d for each dietary treatment before samples were collected. When ruminal fluid from unadapted animals was used, both monensin and laidlomycin propionate decreased (P<.05) CH4 concentration and the acetate:propionate ratio with ground corn and alfalfa hay. Monensin reduced (P<.05) in vitro dry matter disappearance of alfalfa and increased (P<.05) final pH in the ground corn and alfalfa hay fermentations. Both laidlomycin propionate and monensin decreased (P<.05) concentrations of acetate, propionate, isobutyrate, isovalerate, CH4, and NH3 in Trypticase fermentations. When ruminal fluid from adapted animals was used, both ionophores still reduced the concentrations of most fermentation products. However, there was generally less inhibition compared with fermentations inoculated with unadapted mixed ruminal microorganisms. In the presence of 5 mM maltose, mixed ruminal bacteria produced high concentrations (10 to 11 mM) of lactate, and addition of both ionophores to these fermentations was effective in reducing (P<.05) lactate production. In conclusion, laidlomycin propionate alters the mixed ruminal microorganism fermentation in a manner similar to monensin, but, at the concentrations used in this study, monensin seemed to be a more potent inhibitor.     

Characterization of dietary protein in Brassica carinata meal when used as a protein supplement for beef cattle consuming a forage-based diet

As a novel oilseed crop in Florida, Brassica carinata has the capacity of producing high-quality jet biofuel, with a protein-dense meal (~40% crude protein; CP) obtained as a by-product of oil extraction. Characterization of the meal protein is limited, yet necessary for formulation of beef cattle diets; therefore, the objective of this experiment was to determine ruminal and postruminal digestibility of protein from B. carinata. Eight ruminally cannulated Angus crossbred steers (473 ± 119 kg) were used in a duplicated 4 × 4 Latin square design, in which in situ ruminal and postruminal degradability of nutrients were evaluated. The three-step in vitro procedure was used to compare CP and amino acid (AA) degradation in B. carinata meal pellets (BCM) with that of cottonseed meal (CSM), dry distillers grains with solubles (DDGS), and soybean meal (SBM). In situ bags were incubated in the rumen for 0 to 96 hr, with the undegraded supplement remaining after 16 hr subjected to serial in vitro enzymatic solutions. Data were analyzed using the MIXED procedure of SAS. Ruminal rate of degradation of dry matter, organic matter, and CP was greatest (P ˂ 0.01; 10.9, 11.3, and 11.5 %/h, respectively) for SBM. Rumen degradable protein (RDP) content did not differ (P = 0.20; 47.8% and 55.1%, respectively) between CSM and DDGS, but was decreased (P ˂ 0.01) compared with SBM and BCM, which did not differ (P = 0.99; 72.3% and 71.8% RDP, respectively). Compared with DDGS, SBM had greater (P < 0.01) intestinal digestibility of rumen undegradable protein (RUP). Intestinally absorbable digestible protein (IADP) was greatest (P < 0.01) for CSM, with SBM and BCM having the least IADP. Total tract digestibility of CP (TTDP) was greater (P < 0.01) for SBM compared with CSM and DDGS. The contribution of RUP to intestinally absorbable AA was 7.2 and 3.1 g of lysine and methionine per kilogram of CP in BCM, respectively. The evaluation of B. carinata meal as protein supplemented for cattle consuming a forage-based diet resulted in 71.8% RDP and 97.1% TTDP, thus indicating its viability as a high-quality protein supplement for beef cattle.     

Effects of increasing level of supplemental barley on forage intake, digestibility, and ruminal fermentation in steers fed medium-quality grass hay

Objectives of this research were to evaluate effects of increasing level of barley supplementation on forage intake, digestibility, and ruminal fermentation in beef steers fed medium-quality forage. Four crossbred ruminally cannulated steers (average initial BW = 200 +/- 10 kg) were used in a 4 x 4 Latin square design. Chopped (5 cm) grass hay (10% CP) was offered ad libitum with one of four supplements. Supplements included 0, 0.8, 1.6, or 2.4 kg of barley (DM basis) and were fed in two equal portions at 0700 and 1600. Supplements were fed at levels to provide for equal intake of supplemental protein with the addition of soybean meal. Forage intake (kg and g/kg BW) decreased linearly (P < 0.01), and total intake increased linearly (P < 0.03) with increasing level of barley supplementation. Digestible OM intake (g/kg BW) increased linearly (P < 0.01) with increasing level of barley supplementation; however, the majority of this response was observed with 0.8 kg of barley supplementation. Treatments had only minor effects on ruminal pH, with decreases occurring at 15 h after feeding in steers receiving 2.4 kg of barley supplementation. Total-tract digestibility of DM, OM, NDF, and CP were increased (P < 0.04) with barley supplementation; however, ADF digestibility was decreased by 1.6 and 2.4 kg of barley supplementation compared with controls. Ruminal ammonia concentrations decreased linearly (P < 0.01) at 1 through 15 h after feeding. Total ruminal VFA concentrations were not altered by dietary treatments. Ruminal proportions of acetate and butyrate decreased (P < 0.10) in response to supplementation. Rate, lag, and extent (72 h) of in situ forage degradability were unaffected by treatment. Generally, these data are interpreted to indicate that increasing levels of barley supplementation decrease forage intake, increase DM, OM, and NDF digestibility, and indicate alteration of the ruminal environment and fermentation patterns.     

Supplemental cracked corn for steers fed fresh alfalfa: II. Protein and amino acid digestion

The effects of different levels of cracked corn on N intake, ruminal bacterial CP synthesis, and duodenal flows and small intestinal digestion of amino acids (AA) in steers fed fresh alfalfa indoors were determined. Angus steers (n = 6; average BW 338 +/- 19 kg) cannulated in the rumen, duodenum, and ileum were fed each of five diets over five periods in a Latin square design with an extra animal. Steers consumed 1) alfalfa (20.4% CP, 41.6% NDF) ad libitum (AALF); 2), 3), and 4) AALF supplemented (S) with three levels of corn (.4, .8, or 1.2% of BW, respectively), or 5) alfalfa restricted (RALF) to the average forage intake of S steers. Average N intake and duodenal flow of nonammonia N (NAN) were greater (P < .01) in S than in RALF steers. Greater duodenal flows of NAN in S compared with RALF were due to a trend toward higher (P = .06) flows of both bacterial and dietary N. Levels of corn decreased (P < .01) linearly N intake and increased (P < .01) linearly duodenal flow of NAN owing to a numerical linear increase in nonbacterial N (P = .15) with no increase in bacterial N flow. Duodenal NAN flows as percentages of N intake increased (P < .01) linearly (69.3 to 91.0%) as corn increased. Ruminal NH3 N concentration, ruminal CP degradability, and the proportion of bacterial N in duodenal NAN were decreased (P < .01) linearly as corn increased. Efficiency of net microbial CP synthesis was not affected (P > .05) by treatment (average 42.6 and 30.9 g N/kg of OM apparently or truly digested in the rumen, respectively). Small intestinal disappearance of total N and individual AA, except for threonine and lysine, and small intestinal digestibility of N and individual AA, except for methionine, histidine, and proline, increased (P < .01) linearly with level of corn and were greater (P < .01) in S than in RALF steers. Supplementing corn to steers fed fresh alfalfa reduced ruminal N losses and CP degradability and increased the duodenal flow and the small intestinal disappearance and digestibility of total N and total, essential, and nonessential AA.     

Effects of a monensin ruminal delivery device on daily gain, forage intake and ruminal fermentation of steers grazing irrigated winter wheat pasture

Two trials evaluated the effects of a monensin ruminal delivery device (MRDD) on steers grazing winter wheat pasture. In Trial 1, 60 Hereford steers (initial wt 238.5 kg) grazed a 21.9-ha paddock of Vona-variety winter wheat for 112 d. Steers were assigned to either MRDD or control (C) treatments in a randomized complete block design. In Trial 2, eight ruminally cannulated steers (avg wt 234.4 kg) grazed a 2.4-ha paddock of Vona-variety wheat and were assigned randomly to either MRDD or C treatments. Three 11-d collection periods were conducted during early February, early March and early April. Chromic oxide was dosed to determine fecal output, and ruminal samples were collected on d 6 of each period. Nylon bags containing ground wheat forage were incubated ruminally beginning on d 8. In Trial 1, steers with MRDD tended (P less than .11) to gain more weight than C steers (.44 vs .38 kg/d). In Trial 2, wheat forage intake, in situ DM disappearance, ruminal pH, ruminal ammonia concentrations and ruminal proportions of acetate and total VFA concentrations were not affected by treatment. Ruminal proportions of propionate were increased (P less than .05) slightly by MRDD (20.3 and 19.2 mol/100 mol for MRDD and C, respectively). Butyrate proportions in ruminal samples were decreased (P less than .05) by MRDD during March but not in other sampling periods. Ruminal fluid chlorophyll concentration was less (P less than .05) for MRDD-treated vs C steers during early March but was greater (P less than .10) for MRDD-treated steers during early April. The MRDD shows promise as a method of supplying monensin to cattle grazing winter wheat forage.     

Effects of protein supplementation to steers consuming low-quality forages on greenhouse gas emissions

Providing supplements that enhance the efficiency of feed utilization can reduce methane (CH₄) emissions from ruminants. Protein supplementation is widely used to increase intake and digestion of low-quality forages, yet little is known about its impact on CH₄ emissions. British-cross steers (n = 23; initial body weight [BW] = 344 ± 33.9 kg) were used in a three-period crossover design to evaluate the effect of protein supplementation to beef cattle consuming low-quality forage on ruminal CH₄, metabolic carbon dioxide (CO₂) emissions, forage intake, and ruminal fermentation. Steers individually had ad libitum access to low-quality bluestem hay (4.6% crude protein [CP]) and were provided supplemental protein based on (dry matter basis): cottonseed meal (CSM; 0.29% of BW daily; 391 g/d CP), dried distillers grains with solubles (DDGS; 0.41% of BW daily 563 g/d CP), or none (CON). Urea was added to DDGS to match rumen degradable protein provided by CSM. Ruminal CH₄ and metabolic CO₂ fluxes were obtained 2.4 ± 0.4 times per steer daily using an automated open-circuit gas quantification system (GreenFeed emission monitoring system; C-Lock Inc., Rapid City, SD). Forage intake increased (P < 0.01) with protein supplementation; however, no difference in forage intake (P = 0.14) was observed between CSM and DDGS treatments. Flux of CO₂ (g/d) was greater (P < 0.01) for steers fed CSM and DDGS than for steers fed CON. Steers supplemented with CSM had greater (P < 0.01) CH₄ emissions (211 g/d) than DDGS (197 g/d) both of which were greater (P < 0.01) than CON (175 g/d). Methane emissions as a proportion of gross energy intake (GEI) were lowest (P < 0.01) for DDGS (7.66%), intermediate for CSM (8.46%) steers, and greatest for CON (10.53%). Steers fed DDGS also had the lowest (P < 0.01) ruminal acetate:propionate ratio (3.60), whereas CSM (4.89) was intermediate, and CON (5.64) steers were greatest. This study suggests that the common practice of supplementing protein to cattle consuming low-quality forage decreases greenhouse gas emissions per unit of GEI.