Influence of supplementation on behavior of grazing cattle.

Dormant grasses are usually deficient in nutrients needed to meet cattle requirements. Research results indicate that grazing activities are sensitive to some environmental variables and vegetative (sward) characteristics; however, minimal information is available on the influence of supplementation regimens on cattle grazing activities. Supplementation studies reviewed had forage N levels that ranged from .9 to 1.2% and forage intakes that ranged from 12.3 to 31.0 g of OM/kg of BW. Protein supplementation affected (P < .05) time spent grazing: unsupplemented (NS) cattle grazed approximately 1.5 h/d more than did supplemented (S) cattle. Type of supplemental protein and time of daily feeding did not affect (P > .10) this response. Different types and timing of starch-based supplements produced variable results; however, increasing the level of supplemental starch decreased (P < .05) daily grazing time. Protein supplementation increased (P < .05) harvesting efficiency (HE; grams of forage intake.kilogram of BW-1.minute spent grazing-1); however, high-starch supplements either did not alter (P > .10) or decreased (P < .05) HE compared with NS. Progressive defoliation can influence grazing behavior in both sheep and cattle grazing actively growing forage; however, evaluation of vegetative characteristics of dormant forage and the corresponding effect on grazing behavior are not known. The effects of various grazing management strategies on cattle behavior are inconclusive and deserve additional attention. Methods and (or) management practices that modify behaviors to control feed intake, improve efficiency, or reduce stress could be major contributions to the livestock industry.

Influence of ruminal or duodenal soybean oil infusion on intake, ruminal fermentation, site and extent of digestion, and microbial protein synthesis in beef heifers consuming grass hay.

Six heifers (two Hereford X Jersey, four Hereford X Longhorn; average BW 278 kg) cannulated at the rumen and duodenum and fed a grass hay (fescue/orchardgrass) diet were used in a replicated 3 X 3 Latin square. Treatments were either no infusion (C), 150 ml of duodenally infused soybean oil (DI), or 150 ml of ruminally infused soybean oil (RI)/heifer twice daily for a total daily infusion of 300 ml of soybean oil. Periods of the Latin square included 18 d for adaptation and 5 d for collection. Forage OM, ADF, NDF, and N intakes were not affected (P greater than .10) by soybean oil infusion. Ruminal (P = .11) and total tract (P less than .10) OM digestibilities were decreased by RI compared with C or DI, but ADF and NDF digestibilities were not affected by treatment. Duodenal N (P less than .05) and microbial N flows were increased (P less than .10) for C and RI compared with DI. Microbial efficiency (g of N/kg of OM truly fermented) was improved (P less than .10) by RI compared with DI but did not differ (P greater than .10) from C. Ruminal pH was lower (P less than .05) with RI than with either C or DI. Ruminal NH3 N, total VFA, and acetate were not affected (P greater than .10) by treatment. Propionate (mol/100 mol) was greater (P less than .05) with RI than with DI and C, but the proportion of butyrate did not differ among treatments. These data indicate minimal direct benefits for improving forage usage as a result of soybean oil infusion with a 100% grass diet; however, animals should realize benefits from additional dietary energy provided by infused lipid.

Estimating diet digestibility: a comparison of 11 techniques across six different diets fed to rams.

Six digestion trials were conducted using eight Suffolk rams (four/trial; two trials run concurrently) to determine the ability of 11 techniques to estimate in vivo apparent DM digestibility (DMD). Diets (trials) were as follows: 1) ad libitum access to chopped fescue hay, 2) ad libitum access to alfalfa hay, 3) limit-fed fescue hay, 4) limit-fed alfalfa hay, 5) 25% soybean meal and 75% fescue hay and 6) 40% rolled corn and 60% alfalfa hay. Total feces were collected for 7 d following a 21-d adaptation to each diet. Digestibility methods evaluated were the following: 1) in vitro disappearance (INVITRO); 2) 48 h and 3) 72 h in situ nylon bag (48NB, 72NB); 4) 48NB followed by a 48-h acid pepsin digestion; 5) 96 h and 6) 144 h in vitro fermentation followed by NDF analysis (INDF96 and INDF144) 7) 96 h and 8) 144 h in vitro fermentation followed by ADF analysis (IADF96 and IADF144); 9) ADL ratio; 10) alkaline hydrogen peroxide treatment before ADL analysis (APFPRE) and 11) alkaline hydrogen peroxide treatment after ADF extraction of ADL (ADLPST). Apparent in vivo DMD was accurately estimated (P greater than .10) by INVITRO, ADL and APLPST with Diet 1. However no marker accurately estimated in vivo DMD when fescue was limit-fed. Apparent DMD of Diet 2 was accurately predicted (P greater than .10) by INVITRO, but when Diet 2 was limit-fed, only 48NB and 72NB predicted (P greater than .10) DMD accurately. In vivo DMD coefficients for Diet 5 followed a pattern similar to that of Diet 1. Diet 6 was predicted by INVITRO, 48NB, INDF96, INDF144 and IADF96 (P greater than .10). Results suggest that caution should be exercised when using these techniques, because no single technique provided accurate estimates across all diets and feeding conditions.

Influence of branched-chain fatty acid supplementation on voluntary intake, site and extent of digestion, ruminal fermentation, digesta kinetics and microbial protein synthesis in beef heifers consuming grass hay.

Four heifers (British x British; average BW 372 kg) cannulated at the rumen and duodenum and consuming a grass hay (fescue-orchardgrass) diet were used in a 4 x 4 Latin square and supplemented with four levels (0, 20, 40, and 60 g.head-1.d-1) of supplemental four- and five-carbon VFA (BCFA). Forage OM, ADF, NDF and N intakes and digestibilities were not affected (P greater than .10) by BCFA supplementation. Likewise, duodenal N (microbial, feed and ammonia) flows and microbial efficiency were not altered (P greater than .10) by BCFA supplementation. Neither particulate and fluid passage rate nor in situ rate of NDF digestion was affected (P greater than .10) by treatment. Ruminal pH, ammonia concentrations and total VFA concentrations were similar (P greater than .10) among treatments. Ruminal proportions of acetate and propionate were not affected (P greater than .10) by treatment; however, butyrate responded in a cubic (P less than .05) fashion to BCFA, with the lowest proportion of butyrate at the 40 g BCFA feeding level. A time x treatment interaction (P less than .05) was noted for isobutyrate, isovalerate and valerate proportions; they were increased as a function of BCFA dosage at 2 to 8 h postdosing. Supplemental four- and five-carbon VFA had no effect on digestion and fermentation of grass hay. Supplementation of low-quality roughages with BCFA is not justified.

Thirty or sixty percent milk replacer reduction for calves: effects on alfalfa hay intake and digestibility, digestive kinetics and ruminal fermentation.

Twelve artificially reared, male Holstein calves, ruminally cannulated at 53 d of age, were used in a split-plot design to study the effects of no milk replacer reduction (CON), or reduction by 30% (30R) or 60% (60R) of this value on alfalfa hay intake and digestibility, ruminal fermentation and digestive kinetics. Milk replacer reduction began at 53 d of age and continued until 135 d of age, after which no milk replacer was fed. All calves had ad libitum access to long-stemmed alfalfa hay from birth. Five collection periods were conducted at average calf ages of 72, 87, 108, 129 and 151 d. Reducing the amount of milk replacer fed resulted in a linear increase (P less than .05) in forage OM intake; however, total OM intake (forage + milk) was not different (P greater than .10) among milk reduction groups. Size of particles in feces exhibited quadratic effects in response to milk replacer reduction (P less than .05) but only in the small (less than 150 microns) size groupings. Ruminal pH and ammonia and individual VFA concentrations (except isobutyrate) were not altered by milk reduction (P greater than .10) but increased (P less than .01) with calf age. Milk replacer reduction had a quadratic effect (P less than .05) on fluid outflow rate from the rumen, increasing as milk replacer was reduced. Other fluid and particulate kinetic data, as well as NDF digestion rate and DM digestion showed no effects (P greater than .10) from milk replacer reduction but changed with calf age. Milk replacer reduction increased forage intake but had minimal effects on digestive variables evaluated, suggesting that intake of milk replacer by calves can be reduced by up to 60% without disturbing forage fermentation and passage.

Steers grazing blue grama rangeland throughout the growing season. I. Dietary composition, intake, digesta kinetics and ruminal fermentation.

Four sampling periods on blue grama rangeland in northeastern New Mexico evaluated effects of advancing forage maturity and drought-induced dormancy on dietary nutrient and botanical composition, intake, digesta kinetics and ruminal fermentation in grazing beef steers. Six ruminally cannulated and three esophageally cannulated steers freely grazed a 12-ha pasture during the study. Sampling periods lasted 11 d and started June 2, during the early growing season (EGS); June 22, during early summer dormancy (ESD); July 21, during late summer dormancy (LSD); and August 25, 1985, during the late growing season (LGS). Forage availability was not limiting in any sampling period. Steers consumed a greater (P less than .05) percentage in forbs and lower percentage of grasses in EGS and ESD than in LSD and LGS. Dietary in vitro organic matter digestibility was lower (P less than .05) in ESD than in EGS, LSD and LGS. Dietary N content was higher (P less than .05) in EGs and LGS than in ESD and LSD. Neutral detergent fiber content was lower (P less than .05) in EGS than in other sampling periods, while dietary lignin contents were similar for all sampling periods. Voluntary organic matter intake was similar for all sampling periods; however, estimated gastrointestinal tract fill was greater (P less than .05) in ESD and LSD than in EGS and LGS. Particulate passage rate was slower (P less than .05) and total mean retention time longer (P less than .05) in LSD than in other sampling periods. Rate and lag time of neutral detergent fiber digestion were not different among sampling periods. Ruminal pH was greater (P less than .05) at 3 and 6 h after sunrise in ESD than in other sampling periods. Ruminal ammonia concentrations were lower (P less than .05) in ESD and LSD than in EGS and LGS at 3 and 6 h after sunrise. Total volatile fatty acid concentrations were lower (P less than .05) in ESD than in EGS and LSD at 3 h after sunrise and lower (P less than .10) than EGS and LGS at 9 h after sunrise. Molar proportions of acetate were greater (P less than .05) at 3 h after sunrise in ESD and LSD than in EGS and LGS. Changes in digesta kinetics and ruminal fermentation patterns observed in this study appeared to be related to both forage maturity and dietary botanical composition.

Forage intake and digestion by cattle grazing midgrass prairie rangeland or sideoats grama/sweetclover pasture.

In mid-May, beef cattle fitted with esophageal (four steers/pasture) or ruminal and duodenal cannulas (six heifers/pasture; 274 +/- 6 kg BW +/- SE) grazed midgrass prairie (excellent range condition; PRAIRIE) or a seeded mixture of sideoats grama (48% of pasture DM) and sweetclover (6% of pasture DM; Bouteloua curtipendula [Michx.] Torr./Melilotus officinalis [L.] Lam.; PASTURE). Masticate NDF, ADF, and in vitro OM disappearance did not differ (P > .11) between forage types (average = 66.6, 36.1, and 58.8% of OM). Only N differed (P = .02) between PRAIRIE (2.1) and PASTURE (2.4% of OM). Extents of in situ OM and N disappearance were greater (P < .05) and rate of N disappearance between 12 and 36 h was slower (P < .10) from PRAIRIE than from PASTURE masticate. Based on in situ data, the ruminally degraded N: ruminally degraded OM (grams/kilogram) ratio differed (P < .05) between PRAIRIE (22) and PASTURE (25). Ruminal ammonia N concentration (milligrams/deciliter) was less (P = .02) for PRAIRIE (2.8) than for PASTURE (3.8). Forage OM intake and fecal OM output did not differ (P > .72; average = 8,207 and 3,380 g/d), but duodenal OM flow tended (P = .13) to be greater (PRAIRIE = 4,892, PASTURE = 5,170 g/d) in cattle grazing PASTURE. Apparent and true ruminal OM digestion did not differ between forage types (P > .18; average = 38.3 and 48.5%). Nitrogen intake, nonammonia N, and forage N flow at the duodenum were greater (P < .04) for PASTURE (198 vs 171, 242 vs 210, and 162 vs 135 g/d) than for PRAIRIE. Microbial N flow (average = 78 g/d) and microbial efficiency (average = 20 g of microbial N/kg of OM truly fermented) did not differ (P > .25) between forage types. Apparent and true ruminal N digestion did not differ (P > .65; average = -26.6 and 19.3%) between forage types. Flow of nonammonia N was in excess relative to digestible OM intake; hence, digestible OM intake seemed to be first-limiting for performance by cattle grazing either forage type.

Supplemental methionine and time of supplementation effects on ruminal fermentation, digesta kinetics, and in situ dry matter and neutral detergent fiber disappearance in cattle.

Two experiments were conducted to study the effects of methionine supplementation on ruminal fermentation and digesta kinetics. In Exp. 1, nine ruminally cannulated beef heifers (average initial BW = 527 kg) in a crossover design were fed low-quality grass hay and cottonseed meal with or without 11.4 g of supplemental methionine (polysaccharide-coated). Particulate and fluid kinetics, rate of DM and NDF disappearance, ruminal VFA and NH3 N concentrations, and pH were not altered (P > .10) by supplemental methionine; however, ruminal purine concentration was greater (P < .05) in methionine-supplemented heifers than in unsupplemented heifers. In Exp. 2, 12 ruminally cannulated Holstein steers (average initial BW = 622 kg) grazing a fescue pasture were allotted to one of three groups: no supplemental methionine (CON) or 11.4 g of supplemental methionine fed at 0700 (AM) or at 1200 (PM). Forage intake, particulate kinetics, ruminal fluid kinetics, pH, VFA, and NH3 N concentrations were not altered (P > .10) by supplemental methionine or supplementation time. In situ rate of DM and NDF disappearance was greater (P < .05) in supplemented steers than in CON steers; AM steers exhibited faster (P < .05) rates than PM steers. Overall, methionine supplementation of low-quality forage increased ruminal purine concentration but did not alter in situ fermentation or digesta passage, whereas supplementation at 0700, but not at 1200, of steers grazing fescue forage increased rate of NDF fermentation.

Steers grazing endophyte-free tall fescue: seasonal changes in nutrient quality, forage intake, digesta kinetics, ruminal fermentation, and serum hormones and metabolites.

Six ruminally cannulated Holstein steers (average BW 514 kg) grazed a 33-ha, unirrigated, endophyte-free, tall fescue (Festuca arundinacea Schreb.) pasture from April 10 through December 7, 1989. Samples were collected in May, June, September, and November 1989. Total masticate N was relatively constant (P > .10) throughout the year. Masticate in vitro OM disappearance was less (P < .05) in September (48.4%) and November (50%) than in May (60.6%) and June (56%). Ruminal NH3N concentrations (milligrams/deciliter) were greater (P < .05) during May (20.5) and June (17.8) than during September (9.4) and November (5.9). Organic matter intake (grams/kilogram of BW) and particulate passage rate (percentage/hour) were least (P < .05) in November (15.3; 2.6) and not different (P > .10) during May (23.7; 3.1), June (20.7; 3.1), and September (21.0; 3.0). Extent and rate of NDF digestion and ruminal total VFA did not differ (P > .10) across sampling dates. Serum glucose concentrations were not affected (P > .10) by sampling date, but serum urea N was greater (P < .05) during May and November than during June and September. Nonesterified fatty acid concentrations increased (P < .05) with advancing plant maturity. Serum insulin concentrations were greater (P < .05) during May than during other sampling periods; however, growth hormone concentrations were not altered (P > .10) by advancing plant maturity. Unirrigated fescue pasture maintained a high nutrient level throughout the grazing season, and masticate samples did not display the decrease in nutrient content often noted with other types of pasture forage.

Influence of cottonseed meal supplementation on voluntary intake, ruminal and cecal fermentation, digesta kinetics and serum insulin and growth hormone in mature ewes fed prairie hay.

To determine the influence of protein supplementation on intake and fermentation of low-quality hay, six ruminal- and cecal-cannulated Rambouillet ewes (avg wt 43.6 kg) in a crossover design were given ad libitum access to prairie hay with or without 80 g of cottonseed meal (CSM) X head-1 X d-1. Voluntary hay intake was measured the last 7 d of each 18-d period. Ruminal, cecal and blood samples were collected at 0, 1 (except cecal), 3, 6, 9, 12, 15, 18, 21 and 24 h post-supplementation on d 14 of each period to measure fluid dilution rate, fermentation characteristics and serum concentrations of insulin and growth hormone. An intraruminal dose of Yb-labeled hay, followed by fecal sampling on d 15 through 18, was used to measure particulate passage rate. Voluntary intake of prairie hay was increased (P less than .04) from 23.7 to 28.3 g/kg of body weight by CSM supplementation. Particulate passage rate constants did not differ (P greater than .15) between supplemented (3.76%/h) and control (3.72%/h) ewes, and total mean retention time was not altered (P greater than .15) by CSM supplementation. Ruminal retention time of particulates did not differ (P greater than .15) between treatments; however, intestinal transit time was faster (P less than .03; 18.1 vs 22.6 h) in supplemented than in control ewes. Estimated gastrointestinal dry matter fill was greater (P less than .05; 14.3 vs 12.9 g/kg body weight) in supplemented ewes. Ruminal fluid volume did not differ (P greater than .15) between treatments; however, supplemented ewes tended to have faster fluid dilution rates (P less than .14) and fluid outflow rates (P less than .11) than control ewes. Cecal fluid volume, dilution rate and outflow rate did not differ (P greater than .15) between groups. Ruminal and cecal pH and total volatile fatty acids were similar between treatments. Similarly, cottonseed meal supplementation did not affect (P greater than .15) ruminal or cecal ammonia concentrations. Molar proportions of ruminal and cecal individual fatty acids were not affected (P greater than .15) by CSM supplementation. Feeding cottonseed meal increased (P less than .05) serum insulin, decreased (P less than .07) serum growth hormone and increased (P less than .06) serum free fatty acids, but did not influence (P greater than .15) either serum urea N or glucose concentrations. Cottonseed meal supplementation in ewes fed prairie hay caused increased hay intake but had minimal effects on ruminal and cecal fermentation.

Growth performance, serum hormones, and metabolite responses before and after weaning in lambs weaned at 42 days of age: effect of preweaning milk and postweaning alfalfa or grass hay diets.

Fourteen fall-born lambs were used to determine the effects of diet before and after weaning on intake, growth, serum hormones, and metabolite profiles. Before weaning, lambs were intensively sampled for 6 h at 35 and 42 d of age. Before sample collection, lambs were allowed to suckle, and milk intake was recorded. At 42 d of age, lambs were weaned and randomly allotted to ad libitum access to either alfalfa or grass hay. Blood samples were collected at 49 and 56 d of age for 6 h. Milk intake did not differ (P greater than .10) between groups. After weaning, lambs fed alfalfa hay consumed more (P less than .05) hay and had greater (P less than .05) ADG than lambs fed grass hay. Postweaning diet had no effect (P greater than .10) on serum insulin, growth hormone (GH), insulin:GH ratio, prolactin, cortisol, glucose, or nonesterified fatty acids (NE-FA) concentrations. Lambs consuming alfalfa had higher (P less than .05) serum urea nitrogen (SUN) at 49 and 56 d of age than lambs consuming grass. At 35 and 42 d of age, (P less than .05) serum insulin and insulin:GH ratio were higher (P less than .05) after milk intake than at 49 and 56 d of age after hay intake. Serum GH was higher (P less than .05) in lambs at 35 and 42 d of age for 2 h postfeeding, but by h 3 through 5, lambs consuming milk had lower (P less than .05) values than lambs consuming hay.(ABSTRACT TRUNCATED AT 250 WORDS)

Influence of soybean meal and sorghum grain supplementation on intake, digesta kinetics, ruminal fermentation, site and extent of digestion and microbial protein synthesis in beef steers grazing blue grama rangeland.

Six beef steers (British x Brahman) cannulated at the rumen, duodenum and ileum (avg wt 334 kg) and three mature steers (British x British) cannulated at the esophagus were used in a replicated 3 x 3 latin square design and fed no supplement (C), .5 kg soybean meal (SBM) or .5 kg steam-flaked sorghum grain (SFS).head-1.d-1 (DM basis) while grazing blue grama rangeland. Periods of the latin square included a minimum of 14 d for adaptation and 11 d for esophageal masticate collection and digesta sampling. In September, October and November, respectively, forage collected by esophageally cannulated steers averaged 74.5, 88.8 and 71.0% grasses; 2.06, 1.53 and 1.77% N and 68.3, (P greater than .10) by treatment, but total N intake was greater (P less than .05) for SBM vs C and SFS treatments. No differences (P greater than .10) were detected among treatments in OM, NDF, ADF and N digestibilities in the rumen, small intestine or hindgut, but total tract OM digestibility was greater (P less than .10) for SBM and SFS than for C, and total tract N digestibility was greater (P less than .10) for SBM than for C or SFS. Duodenal ammonia N flow was greater (P less than .05) when SBM was fed that when SFS and C were fed, but microbial N and non-ammonia, non-microbial N flows and microbial efficiency were not altered by treatment. Likewise, ileal N flow was not affected (P greater than .10) by treatment. Particulate passage rate, gastrointestinal mean retention time, forage in vitro OM disappearance and in situ rate of forage NDF digestion also were not affected (P greater than .10) by treatments. Ruminal fluid volume was greater (P less than .05) for SFS vs SBM and C treatments, but no differences were noted in fluid dilution rate. Ruminal fluid ammonia concentration was greater (P less than .05) when SBM was fed than when SFS and C were fed (13.5, 9.9 and 8.7 mg/dl, respectively), whereas pH and total VFA concentrations were not different (P greater than .10). Proportion of acetate in ruminal fluid was less (P less than .10) for SBM and SFS than for C. Small amounts of supplemental SBM and SFS had little effect on forage intake, ruminal fermentation and site of digestion but both increased total tract OM digestion in steers grazing blue grama rangeland.

Steers grazing intermediate wheatgrass at various stages of maturity: effects on nutrient quality, forage intake, digesta kinetics, ruminal fermentation, and serum hormones and metabolites.

Six ruminally cannulated Holstein steers (average BW of 495 +/- 5 kg) grazed a 32-ha, nonirrigated, intermediate wheatgrass (Thinopyrum intermedium Host) pasture from April 10 through December 7. Sample collections were conducted in May, June, September, and November 1989. Total masticate N decreased (P < .05) and bound N increased (P < .05) with advancing forage maturity. Masticate in vitro OM disappearance was lower (P < .05) in November (40.5%) than in May (62.0%). Organic matter intake (grams/kilogram of BW) decreased (P < .05) at each sampling date (May = 35.7, June = 26.8, September = 20.0, November = 14.9). Correspondingly, particulate passage rate decreased and gastrointestinal mean retention time increased (P < .05) with advancing forage maturity. Extent and rate of NDF digestion were greater (P < .05) during May and June than during September and November. Ruminal NH3 N and total VFA concentrations were greater (P < .05) during May and June than during September and November. Advancing forage maturity did not alter (P > .10) serum growth hormone concentrations; however, nonesterified fatty acid concentrations were greater (P < .05) during September and November than during May and June. Serum insulin-like growth factor I decreased (P < .05) with advancing forage maturity. Seasonal changes in forage intake and ruminal fermentation suggest that animal performance might be increased if supplemental energy is provided early in the growing season of intermediate wheatgrass; however, supplemental protein would likely be needed as wheatgrass matures.

Diet quality and ruminal digestion in beef cattle grazing midgrass prairie rangeland or plains bluestem pasture throughout the summer.

Beef cattle fitted with esophageal (four steers/pasture) or ruminal and duodenal (six calves/pasture; beginning BW +/- SE = 267 +/- 6 kg) cannulas grazed midgrass prairie rangeland (excellent range condition; MIDGRASS) or plains bluestem (Bothriochloa ischaemum var. Plains) pasture (BLUESTEM) in mid-May, late-June, mid-August, and mid-October of 1990 and 1991. Nitrogen in masticate samples collected from MIDGRASS was lowest (P < .05) in June and August across both years. The N in BLUESTEM masticate peaked (P < .05) in August 1990, but N was lowest (P < .05) in August 1991. The detergent fiber content of masticate from both forages increased (P < .05) as the grazing season advanced from May through August; fall regrowth in October occasionally resulted in a small decrease (P < .05) in fiber content. In vitro OM disappearance (IVOMD) followed a pattern similar to N content. The IVOMD of BLUESTEM masticate was greater (P < .05) than that of MIDGRASS masticate. The ruminal ammonia N concentration (milligrams/deciliter) in cattle grazing BLUESTEM (4.5) usually was greater (P < .05) than in cattle grazing MIDGRASS (3.3). In situ OM and N disappearance was greater (P < .05) from BLUESTEM masticate than from MIDGRASS masticate in May, June, and August. The ruminally degraded N:ruminally degraded OM ratio (grams/kilograms) estimated from in situ digestion suggested that cattle grazing MIDGRASS during the mid-summer of both years and BLUESTEM in August 1991 may have been marginally deficient in ruminally degraded N. Plains bluestem pasture would complement MIDGRASS by providing better quality grazing during the mid-summer.

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.

Effects of pregnancy on digesta kinetics and ruminal fermentation in beef cows.

Four pregnant and four nonpregnant, ruminally cannulated beef cows were used to evaluate the effects of the last trimester of pregnancy on digesta kinetics and ruminal fermentation. Before breeding, cows were allotted randomly either to pregnant (PR) or to nonpregnant (NP) groups; PR cows were bred at the first estrus after synchronization. All cows were fed long-stem fescue hay at 15 g of DM/kg of BW based on BW 120 d before parturition of pregnant cows (average BW of 642 kg). Collection periods, each lasting 9 d, began at 96, 68, 41, and 10 +/- 1.3 d before parturition. Particulate passage rate was greater (P < .05) and retention times and gastrointestinal fill were less (P < .05) for PR than for NP cows. Apparent total tract DM digestion, rate and extent (96-h in situ incubation) of NDF disappearance, and ruminal fluid kinetics were not affected (P > .10) by pregnancy. A physiological state x sampling day interaction was noted (P < .05) for ruminal NH3 N, total VFA concentrations, and molar proportions of butyrate. Ruminal pH and individual VFA proportions, however, did not differ (P > .10) between PR and NP cows, except for valerate, which was less (P < .05) for PR than NP cows. Results suggest that in late pregnancy with restricted feeding, passage rate of particulates increases without substantial changes in fermentation or extent of digestion.

Digesta kinetics, ruminal fermentation characteristics and serum metabolites of pregnant and lactating ewes fed chopped alfalfa hay.

Eight ruminally cannulated ewes (four control and four bred; average BW = 85.7 kg), limit-fed alfalfa hay (1.86% BW), were used in two experiments to determine the effects of pregnancy and lactation on digestive function and serum metabolites. Seven-day sampling periods were used starting on d 102, 118 and 132 of gestation (Exp. 1) and d 14 and 32 of lactation (Exp. 2). Particulate (6.8 vs 4.9%/h; PPR) and fluid passage rates (13.9 vs 10.9%/h) were greater (P less than .05) and gastrointestinal mean retention time (28.9 vs 35.7 h) and fluid turnover time (FTT, 7.5 vs 9.5 h) were lesser (P less than .05) in pregnant than in nonpregnant ewes, respectively. Isobutyrate concentration was lower (P less than .05) in pregnant (1.7 mol/100 mol) than in nonpregnant (1.9 mol/100 mol) ewes. No differences (P greater than .10) were noted for any other ruminal fermentation measures between pregnant and nonpregnant ewes. In Exp. 2, no differences (P greater than .10) were noted in digesta kinetics or ruminal fermentation measures except for isobutyrate and isovalerate molar proportions and serum urea N (SUN) concentration. Isobutyrate, isovalerate and SUN concentrations (21.8 vs 26.1 mg/dl) were lower (P less than .05) in lactating ewes than in nonlactating ewes. Gastrointestinal fill (5.7 vs 7.7 g/kg BW) and FTT (9.3 vs 12.7 h) were lesser and DM digestion (66.7 vs 57.4%) was greater (P less than .05) in lactating than in nonlactating ewes. Data suggest that, during pregnancy, passage rate increases occur without affecting DM digestion and that, during lactation, PPR is not affected when ewes are limit-fed.

Supplemental protein for beef cattle grazing dormant intermediate wheatgrass pasture: effects on nutrient quality, forage intake, digesta kinetics, grazing behavior, ruminal fermentation, and digestion.

Sixteen ruminally cannulated yearling beef cattle (British x British; average BW = 295 +/- 25 kg; three steers and one heifer per treatment) grazing dormant intermediate wheatgrass (Thinopyrum intermedium Host) were allotted to four treatments: 1) no supplement (CON); 2) alfalfa hay (ALF; .52% of BW); 3) cottonseed meal (CSM; .22% of BW); and 4) corn gluten meal-wheat bran feed (CGMWBF; .36% of BW). Supplements were formulated (DM basis) so that intakes were isonitrogenous and were provided once daily (0700). Sampling periods were in February (FEB; .96% N in masticate), March (MAR; 1.06% N in masticate), and April (APR; 1.12% N in masticate) following an initial 21-d adaptation period. Daily grazing time was 1.1 to 1.5 h longer (P < .05) for CON cattle than for supplemented cattle. Forage OM intake (OMI) was not altered (P > .15) by supplemental protein; however, total OMI was greater (P < .04) for supplemented than for unsupplemented cattle. Harvesting efficiency (grams of OM intake-kilogram of BW-1.minute spent grazing-1) was greater (P < .05) for cattle fed CSM than for those fed CGF or CON; cattle fed ALF were intermediate in harvesting efficiency. Ruminal fluid kinetics, in situ rate and extent of NDF digestion, and total VFA concentration were not influenced (P > .10) by type of supplemental protein. Ruminal NH3 N concentration exhibited a treatment x sampling time interaction (P < .05). Type of protein supplement did not seem to affect most digestion measures; however, harvesting efficiency was influenced by supplement type.

Time of daily supplementation for steers grazing dormant intermediate wheatgrass pasture.

To compare the effects of time of daily protein supplementation on grazing behavior, forage intake, digesta kinetics, ruminal fermentation, and serum hormones and metabolites, 12 ruminally cannulated Holstein steers (449 and 378 kg average initial and final BW, respectively) were allotted to three groups. Treatments consisted of CON = no supplement, AM = cottonseed meal (.25% of BW) at 0600, and PM = cottonseed meal (.25% of BW) at 1200. Steers grazed a dormant (1.1% N) intermediate wheatgrass (Thinopyrum intermedium Host) pasture. Sampling trials occurred in December, January, and February. Supplementation altered (P = .01) time spent grazing; CON steers grazed approximately 1.5 h longer than supplemented steers. Supplemented steers lost less (P = .02) BW (-40 kg) than CON steers (-75 kg) did. Supplementation did not alter (P greater than .15) forage OM intake; however, total OM intake was greater (P = .01) for supplemented steers (22.3 g/kg of BW) than for CON (18.4 g/kg of BW) steers. Supplementation did not affect (P greater than .15) digesta kinetics. Extent of in situ NDF (96 h) and rate (%/h) of disappearance for supplemented steers was greater (P = .01) than for CON steers. Across all periods, ruminal NH3 N and total VFA concentrations were lower (P = .01) for CON steers than for supplemented steers. Serum insulin (ng/mL) concentration was lower (P = .03) and concentration of serum growth hormone (ng/mL) was higher (P = .02) for CON steers than for supplemented steers. Cottonseed meal supplementation enhanced utilization of intermediate wheatgrass; however, supplementation time had minimal effects on the variables measured.

Supplemental cracked corn or wheat bran for steers grazing endophyte-free fescue pasture: effects on live weight gain, nutrient quality, forage intake, particulate and fluid kinetics, ruminal fermentation, and digestion.

Two experiments were conducted with beef steers (Exp. 1, average BW of 580 kg; Exp. 2, average BW of 247 kg) to evaluate the use of no supplements (CON) or daily supplementation with (OM basis) .34% of BW of cracked corn (CORN), .34% of BW of wheat bran (WBBW), or .48% of BW of wheat bran (WBISO; calculated to be isocaloric to CORN) on digestive responses (Exp. 1) and live weight gain (Exp. 2). In Exp. 1, type of supplement did not affect (P > .10) the dietary fiber or N constituents, but in vitro OM disappearance of the forage differed (P < .10) with supplementation and type of supplement fed. Supplemented steers consumed less (P < .05) forage and total OM. Particulate passage, fluid passage, and ruminal pH were not affected (P > .10) by supplementation. Ruminal NH3 N concentration showed (P < .05) a treatment x sampling time interaction and, in general, WBBW and WBISO steers had greater ruminal NH3 N than CORN and CON steers. Total VFA concentrations and molar proportions of propionate were lower (P < .10) in CON steers than in supplemented steers; no differences were noted (P > .10) among supplemented steers. Molar proportions of acetate were lower (P = .01) in supplemented steers than in CON steers and were greater (P = .03) in WBBW steers than in WBISO steers. Butyrate molar proportions were lower (P < .05) in CON steers than in supplemented steers and differed (P < .10) with type and quantity of supplement supplied. In situ forage NDF disappearance at 6, 9, and 24 h after feeding and rate of disappearance were greater (P < .05) in CON steers than in supplemented steers. In Exp. 2, CON steers weighed less (P = .01) than supplemented steers, CORN steers weighed more (P = .08) than wheat bran-supplemented steers, and WBISO steers weighed more (P = .02) than WBBW steers; ADG for 90 d followed a similar response. Results suggest that supplementation of wheat bran rather than corn did not seem to stop the reduction in forage intake or OM digestion associated with corn supplementation.