Influence of Jet-Sploding and extrusion on ruminal and intestinal disappearance of canola and soybeans

In situ rumen degradation and intestinal digestibility of DM and CP of Jet-Sploded and extruded protein sources were estimated, using two ruminally and duodenally cannulated lactating Holstein cows, in two experiments. One-gram samples of ground (1 mm) whole canola seed, canola meal, extruded canola meal, Jet-Sploded whole canola seed, Protec, soybean meal and extruded soybean meal (Experiment 1), and whole canola seed Jet-Sploded at temperatures ranging from 116 to 177 degrees C (Experiment 2) were heat sealed into small nylon bags for incubation in the rumen and insertion into the duodenum. Extrusion had no effect on DM or CP disappearance in the rumen nor on effective degradability. Jet-Sploding of whole canola seed dramatically reduced effective degradability (%) of DM (80.5 vs 35.9 at .08 h-1 rumen outflow rate) and CP (83.5 vs. 43.2 at .08 h-1). Total tract disappearance of DM and CP exceeded 90% for all protein sources, except Protec and Jet-Sploded material. Jet-Sploding appears to have potential for decreasing ruminal degradation of canola protein or DM without markedly decreasing intestinal digestibility.     

Comparison of the in situ and in vivo intestinal disappearance of ruminally protected methionine

We designed a switchback expriment to compare the intestinal disappearance of ruminally protected Met determined in situ or in vivo over three consecutive periods. Four nonlactating Holstein heifers (477+/-36 kg) with cannulae in the rumen, duodenum, and ileum were fed a diet based on timothy silage to meet requirements for maintenance (dry matter intake = 8.72+/-0.15 kg). A total of 16 bags, containing 1.5 g of ruminally protected Met, were incubated in the rumen (4.5 h) of each cow and transferred to an acid-pepsin solution to simulate the abomasum (2.5 h). Following each incubation, bags were recovered and three bags were dried at 55 degrees C and analyzed for Met. Remaining bags were introduced directly into the duodenal or ileal cannula for the in situ method, while for the in vivo method, the content of remaining bags was transferred into gelatin capsules before their introduction in the duodenal or ileal cannula. Spot samples of digesta were collected during a 96-h period, with Co-EDTA and Cr-mordanted fiber used as indigestible markers to estimate in vivo digestibility. The disappearance of Met in the small intestine determined in vivo tended to be higher than in situ (74.45 vs. 43.65+/-1.79%). Our results indicate that when used to assess intestinal availability of ruminally protected Met, the mobile nylon bag technique can underestimate the true bioavailability of Met.     

Effect of canola fat on ruminal and total tract digestion, plasma hormones, and metabolites in lactating dairy cows.

The effects of canola fat on digestion and metabolism were investigated by incorporating 0, 4.5, 9, 13.2, or 17.4% Jet-Sploded canola seed into a diet containing a 60:40 (DM) concentrate:forage ratio. The diets contained 16.5% CP, 30% alfalfa silage, and 10% whole-crop oat silage on a DM basis and were fed for ad libitum consumption as TMR to 10 ruminally cannulated Holstein cows in early lactation. Jet-Sploded canola seed supplementation did not change ruminal pH or NH3 N concentrations, but VFA concentrations declined with increasing level of inclusion. Apparent digestibilities of DM, OM, CP, NDF, and ADF were unaffected by level of inclusion of Jet-Sploded canola seed, but ether extract digestibility declined linearly, which resulted in similar ether extract absorption across the three diets supplemented with canola fat. Based on in sacco data, the percentages of ruminal digestion of OM and CP declined with increasing inclusion of Jet-Sploded canola seed. Plasma glucose and FFA concentrations tended to respond in a quadratic fashion, plasma insulin concentration declined linearly, and plasma glucagon and somatotropin concentrations were unaffected by dietary treatment. The results indicate that a positive productive response may be expected from dietary inclusion of about 5% Jet-Sploded canola seed, but the benefits of increased energy density associated with higher inclusion levels may be offset by reduced availability of energy in the rumen and decreased fat digestibility postruminally. The substantial effects of time postfeeding on ruminal fermentation and on concentrations of plasma hormone and metabolites in animals fed TMR demonstrate that infrequent sampling can result in misleading results and, thus, invalid interpretation of the influence of dietary fat on these parameters.     

Effect of nylon bag and protozoa on in vitro corn starch disappearance

An in vitro experiment was carried out to study whether the presence of protozoa in nylon bags can explain the underestimation of the in situ degradation of slowly degradable starch. Corn of a high (flint) and a low (dent) vitreousness variety was ground over a 3-mm screen, weighed in nylon bags with a pore size of 37 μ m, and washed in cold water. Samples of washed cornstarch were incubated in 40-mL tubes with faunated and defaunated ruminal fluid. An additional amount of washed corn, in nylon bags, was inserted in each incubation tube. Incubations were carried out for 0, 2, 4, 6, 12, and 24 h, and starch residue in tube and nylon bag was determined. In general, starch disappearance from the nylon bag was less than from the tube, and was less with faunated than defaunated rumen fluid, but corn variety did not affect starch disappearance. When no protozoa were present, the disappearance of starch from the bags was higher after 6 and 12 h incubation compared with presence of protozoa. However, in the tubes, there was no difference in starch disappearance due to presence or absence of protozoa. Estimated lag time was higher in presence (4.6 h) then absence (3.6 h) of protozoa. It was concluded that the effect of presence or absence of protozoa on starch disappearance differs within or outside nylon bags. The reduced disappearance rate of starch inside the nylon bags in the presence of protozoa helps to explain the underestimation of starch degradation based on the in sacco procedure when compared with in vivo data upon incubation of slowly degradable starch sources.     

Influence of prilled fat and calcium salt of palm oil fatty acids on ruminal fermentation and nutrient digestibility

Four rumen cannulated Holstein cows were used in a Latin square design to examine the effect of supplemental calcium salt of palm oil fatty acids (.68 kg/d) or prilled fat (.68 or .91 kg/d) on DM intake, rumen fermentation, and nutrient digestibility. Basal diet contained 45% concentrate, 27.5% alfalfa silage, and 27.5% corn silage (DM basis), and treatments were balanced for calcium. Dry matter intake was similar among treatments. Ruminal pH, total VFA, and molar percentage acetate and propionate were not affected by fat supplementation. Feeding prilled fat decreased slightly ruminal molar percentage butyrate. Forage DM and neutral detergent fiber disappearance from ruminally suspended dacron bags did not differ due to treatment. For unknown reasons, total tract apparent digestibility of DM and NDF was lower when cows received the low amount but not the high amount of prilled fat. Milk yield and fat percentage were not significantly affected by treatment. Milk protein was maintained during prilled fat supplementation but decreased .13% during calcium salt of palm oil fatty acid supplementation. Both fat supplements appeared inert in the rumen and did not markedly affect nutrient digestion when supplemented at 3.5% or less of the total ration DM.     

Intestinal disappearance and mesenteric and portal appearance of amino acids in dairy cows fed ruminally protected methionine

An experiment was conducted to compare the rates of disappearance of amino acids (AA) from the small intestine and their net appearance in the blood draining only the small intestine (mesenteric-drained viscera) and the whole gastrointestinal tract (portal-drained viscera) of cows fed a silage-based diet supplemented or not with ruminally protected Met. Five lactating dairy cows (118+/-4 DIM) equipped with duodenal and ileal cannulae (n = 2) or a duodenal cannula only (n = 3), two of which were multicatheterized, were fed a TMR top dressed with 0 or 72 g of ruminally protected Met per day. The addition of ruminally protected Met to the diet increased the duodenal flux of Met leading to a higher apparent digestibility of Met in the small intestine. Sixty-six percent of Met from ruminally protected Met bypassed the rumen and 82% of that Met disappeared from the small intestine. Arterial plasma Met concentrations numerically increased with ruminally protected Met (45 vs. 18 microM), while total AA concentration decreased. Feeding ruminally protected Met resulted in higher concentrations of urea-N and glucose in arterial plasma. Milk production and milk composition were unaffected. The disappearance of essential AA across the small intestine was equivalent (101%) to their flux through the mesenteric-drained viscera while the portal:mesenteric-drained viscera flux ratio for each essential AA varied from 38% for Thr to 76% for Phe. The portal:mesenteric-drained viscera flux ratio for Met was 66%. These results confirm observations made with pigs and sheep.     

Ruminal degradability of dry matter,crude protein,and amino acids in soybean meal,canola meal,corn, and wheat dried distillers grains

Different protein sources, such as canola meal (CM) or dried distillers grains (DDG), are currently used in dairy rations to replace soybean meal (SBM). However, little data exists comparing their rumen degradation in a single study. Therefore, the objective of this study was to compare the ruminal degradation of dry matter (DM), crude protein (CP), and AA of SBM, CM, high-protein corn DDG (HPDDG), and wheat DDG plus solubles (WDDGS). In situ studies were conducted with 4 rumen-fistulated lactating Holstein cows fed a diet containing 38% grass hay and 62% corn-based concentrate. Each protein source was incubated in the rumen of each cow in nylon bags for 0, 2, 4, 8, 16, 24, and 48 h to determine DM and CP rumen degradation kinetics, whereas additional bags were also incubated for 16 h to evaluate AA ruminal disappearance. Rumen DM and CP degradability was calculated from rumen-undegraded residues corrected or not for small particle loss. Data were fitted to an exponential model to estimate degradation parameters and effective degradability (ED) was calculated with a passage rate of 0.074 h⁻¹. The WDDGS and SBM had higher uncorrected ED (DM = 75.0 and 72.6%; CP = 84.8 and 66.0%, respectively) than CM and HPDDG (DM = 57.2 and 55.5%; CP = 59.3 and 48.2%, respectively), due to higher soluble fraction in WDDGS and a combination of higher potentially degradable fraction and rate of degradation in SBM. Correction for small particle loss from bags, higher for WDDGS than for the other protein sources, decreased estimated ED but did not alter feed ranking. The ruminal disappearance of AA after 16 h of incubation reflected the overall pattern of CP degradation between protein supplements, but the ruminal disappearance of individual AA differed between protein supplements. Overall, these results indicate that, in the current study, (1) SBM and WDDGS were more degradable in the rumen than CM and HPDDG, and (2) that small particle loss correction is relevant but does not alter this ranking.     

Digestion of feed amino acids in the rumen and intestine of steers measured using a mobile nylon bag technique

The disappearance of dry matter (DM), crude protein (CP), and amino acids (AA) in steers after rumen incubation and intestinal passage of alfalfa hay, barley hay, corn silage, barley grain, corn grain, wheat bran, meat meal, fish meal, cottonseed meal, and soybean meal were measured in 3 steers using a mobile nylon bag technique. Ruminal degradation of individual AA differed between feedstuffs. For barley hay and corn silage, the ruminal disappearance of total AA was higher and lower than the other feedstuffs, respectively. The intestinal digestibility of total AA in alfalfa hay was lower than the digestion of CP. The intestinal digestibility of Arg and His was higher than that of total AA in alfalfa hay, meat meal, cottonseed meal, soybean meal, barley hay, and wheat bran. In addition, the intestinal digestibility of Lys was higher than that of total AA in alfalfa hay, meat meal, cottonseed meal, soybean meal, barley hay, corn silage, and wheat bran. The intestinal disappearance of CP in most cases was higher than that of DM. The results indicated that feedstuffs with lower ruminal disappearance of DM, CP, total AA, essential AA, and nonessential AA generally had a higher intestinal disappearance, resulting in a relatively constant total tract disappearance. These results could be used to improve the current system of diet formulation in ruminants.     

Mobile nylon bag for estimating intestinal availability of rumen undegradable protein

The objective was to develop a method for estimating intestinal availability of rumen undegradable protein. One-gram samples of six feedstuffs were placed into small (3.5 X 5.5 cm) nylon bags (pore size 48 micron). Bags were heat sealed and ruminally incubated in a polyester mesh (lingerie) bag in quadruplicate for each of six time periods (0, 2, 4, 8, 12, 24 h). Two bags from each rumen incubation time were inserted into the small intestine via a duodenal cannula at the rate of one bag per 45 min. Bags were mechanically washed either upon removal from the rumen--for determination of rumen degradability, or when recovered from the feces--for estimation of intestinal availability. Dried bags plus contents were digested intact for nitrogen analysis. Rumen degradable protein and apparent intestinal availability of undegradable protein (based on 8 h of rumen incubation) for corn gluten meal, fish meal, meat and bone meal, soybean meal, canola meal, and alfalfa hay, respectively, were 11.8, 95.0; 28.5, 82.8; 46.7, 73.0; 55.1, 99.3; 69.7, 79.2; and 68.8, 71.2. Results support the use of this technique as a rapid method for estimating both ruminal degradability, and intestinal availability of rumen undegradable protein.     

In situ disappearance of malate from alfalfa and bermudagrass hay

The objectives of this study were to determine the rate of malate and dry matter disappearance from different forages in the rumen. Four nonlactating, ruminally cannulated Holstein cows were fed a hay-based diet. Samples of early and late harvested alfalfa, Coastal bermudagrass, and Tifton 85 bermudagrass hays were ground, placed in nylon in situ bags, and ruminally incubated for 0, 0.5, 1, 2, 4, 8, 12, 24, and 48 h. After incubation, samples were rinsed, freeze-dried, extracted, and analyzed for malate content by HPLC with an organic acid column. When forages were incubated in the rumen, malate concentrations were less than 0.55 mg/g of dry matter at 0.5 h and remained low for the 48-h incubation period. These results suggest that malate was solublized and utilized within 30 min after reaching the rumen. Dry matter digestibility of both forages increased with time and was different across forages. Both alfalfa samples were digested to a greater extent between 0.5 and 24 h than either type of bermudagrass, but after 48 h the early maturity Tifton 85 digestibility was similar to alfalfa. Even though it is more common to feed unground forages to ruminants, these in situ results suggest that once malate is available in the rumen it will disappear quickly.     

Technical note: Methodological and feed factors affecting prediction of ruminal degradability and intestinal digestibility of essential amino acids

We hypothesized that ruminal degradability of essential AA (EAA) and the intestinal digestibility of the ruminally undegraded EAA residue in feeds could be evaluated in a meta-analysis. The objective was to characterize methodological factors for ruminal incubation (time of incubation of feed in situ) and method of simulating digestion of the ruminally undegraded AA (incubation of residue in digestive enzymes in vitro or in mobile bags inserted into the duodenum). To increase numbers of observations, feeds were categorized before ANOVA. An approach is described to predict differential ruminal degradability (or undegradability) of individual EAA by normalizing them as a proportion of total AA (TAA) degradability (undegradability) and similarly to normalize the intestinal digestibility of EAA using TAA. Interaction of feed category with individual EAA justifies future studies with a broader range of feeds and more replication within feed to bolster this approach. With broader data, the approach to normalize EAA as a proportion of TAA should allow a better defined EAA library to be integrated with more robust CP databases (that can be updated with specific feed information from more routine laboratory analyses) in dairy supply-requirement models.     

Effects of feeding or abomasal infusion of canola oil in Holstein cows. 1. Nutrient digestion and milk composition

We determined the effects of feeding canola oil or infusing it into the abomasum on rumen fermentation, nutrient digestibility, duodenal flows of fatty acids, and milk composition in Holstein cows. Five ruminally and duodenally cannulated Holstein cows in late lactation were used in a 3 x 5 incomplete Latin square design. Treatments were 1) Control: basal diet (CON), 2) Control+supplementation of canola oil at 1 kg/d in the feed (FED), and 3) Control+abomasal infusion of canola oil at 1 kg/d (INF). Compared with CON, feed intake, ruminal fermentation characteristics, ruminal and total tract digestibilities of nutrients were not significantly affected by FED treatment but duodenal flows and milk concentrations of fatty acids (FA) such as trans-11 18:1 and cis-9 trans-11 18:2 (conjugated linoleic acid, CLA) were increased. In contrast to the effects of FED, INF reduced feed intake, total VFA production, intestinal flows of nutrients, FA digestibility and yields of milk and milk fat. Both FED and INF significantly reduced the proportions of saturated and medium-chain FA, and increased cis 18:1 in milk. Concentrations of 18:2n-6 and 18:3n-3 in milk were increased nearly 2-fold with INF relative to CON. Dietary or postruminal supplementation of canola oil to late-lactation cows reduced saturated FA and increased unsaturated C18 in milk but nutrient digestion was adversely affected with abomasal infusion of canola oil.     

In vitro digestibility of individual amino acids in rumen-undegraded protein: The modified three-step procedure and the immobilized digestive enzyme assay

Three soybean meal, 3 SoyPlus (West Central Cooperative, Ralston, IA), 5 distillers dried grains with solubles, and 5 fish meal samples were used to evaluate the modified 3-step in vitro procedure (TSP) and the in vitro immobilized digestive enzyme assay (IDEA; Novus International Inc., St. Louis, MO) for estimating digestibility of AA in rumen-undegraded protein (RUP-AA). In a previous experiment, each sample was ruminally incubated in situ for 16 h, and in vivo digestibility of AA in the intact samples and in the rumen-undegraded residues (RUR) was obtained for all samples using the precision-fed cecectomized rooster assay. For the modified TSP, 5 g of RUR was weighed into polyester bags, which were then heat-sealed and placed into Daisy^II incubator bottles. Samples were incubated in a pepsin/HCl solution followed by incubation in a pancreatin solution. After this incubation, residues remaining in the bags were analyzed for AA, and digestibility of RUP-AA was calculated based on disappearance from the bags. In vitro RUP-AA digestibility estimates obtained with this procedure were highly correlated to in vivo estimates. Corresponding intact feeds were also analyzed via the pepsin/pancreatin steps of the modified TSP. In vitro estimates of AA digestibility of the feeds were highly correlated to in vivo RUP-AA digestibility, which suggests that the feeds may not need to be ruminally incubated before determining RUP-AA digestibility in vitro. The RUR were also analyzed via the IDEA kits. The IDEA values of the RUR were good predictors of RUP-AA digestibility in soybean meal, SoyPlus, and distillers dried grains with solubles, but the IDEA values were not as good predictors of RUP-AA digestibility in fish meal. However, the IDEA values of intact feed samples were also determined and were highly correlated to in vivo RUP-AA digestibility for all feed types, suggesting that the IDEA value of intact feeds may be a better predictor of RUP-AA digestibility than the IDEA value of the RUR. In conclusion, the modified TSP and IDEA kits are good approaches for estimating RUP-AA digestibility in soybean meal products, distillers dried grains with solubles, and fish meal samples.     

Technical note: assessment of recovery site of mobile nylon bags for measuring ileal digestibility of starch in dairy cows

The objective of this study was to evaluate recovery site of mobile nylon bags for measuring ileal digestibility of ruminally undegraded starch in dairy cows. Eight feed samples of untreated and treated concentrates were examined. Three lactating cows equipped with rumen fistula and duodenal and ileal cannulas were used in the experiment. The mobile nylon bags containing intact feeds or residues after a 12-h ruminal incubation were pretreated using a 2-step procedure to simulate abomasal digestion before insertion through the duodenal cannula. To assess the effect of hindgut fermentation on starch digestibility, approximately half of the bags were collected from the ileum and half from the feces. The results indicate that feed samples should be preincubated in rumen before insertion into duodenum, and that samples with relatively high fractions of rumen-undigestible starch should be collected from the ileum instead of from feces.     

Kinetics of in sacco fiber-attachment of representative ruminal cellulolytic bacteria monitored by competitive PCR

Stems of orchardgrass hay in nylon bags were incubated in the rumens of three ruminally fistulated sheep to monitor the rate and extent of fiber attachment by the representative ruminal cellulolytic bacteria via competitive polymerase chain reaction. After incubation for 5 min, the numbers of Fibrobacter succinogenes and the two ruminococcal species attached to stems were 10(5) and 10(4)/g dry matter (DM) of stem, respectively. At 10 min, the numbers of all three species attached to stems increased 10-fold. Thereafter, attached cell numbers of the three species gradually increased and peaked at 24 h (10(9)/g DM for F. succinogenes and 10(7)/g DM for Ruminococcus flavefaciens) or 48 h (10(6)/g DM for Ruminococcus albus). On the other hand, cell numbers of all three species in the whole digesta were constant over 24 h. Changes in the rate of in sacco neutral detergent fiber disappearance of hay stem, which showed a linear increase up to 96 h, were not synchronized with changes in cellulolytic bacterial mass. These results suggest that sufficient numbers of cells of the three cellulolytic species to move to new plant fragments are present at the start of incubation, the initial attachment to new plant matter is mostly accomplished within 10 min and then bacterial growth and fibrolytic action follow. F. succinogenes was most dominant, both in the whole rumen digesta and on the suspended hay stems, demonstrating the ecological and functional significance of this species in ruminal fiber digestion.     

Ruminal degradability and intestinal digestibility of protein and amino acids in treated soybean meal products

Four lactating dairy cows equipped with ruminal and duodenal cannulas were used to determine the impact of different methods of treating soybean meal (SBM) on the ruminal degradability and intestinal digestibility of crude protein and AA. Solvent-extracted SBM (SE), expeller SBM (EP), lignosulfonate SBM (LS), and heat and soyhulls SBM (HS) were incubated in the rumen in nylon bags for 48, 24, 16, 8, 4, 2, and 0 h according to National Research Council (2001) guidelines. Additional samples of each SBM product were also incubated for 16 h in the rumen; the residues from these bags were transferred to mobile bags, soaked in pepsin HCl, and then used for determination of intestinal digestibility in situ or in vitro. Treatment of SBM (EP, LS, HS) protected the crude protein and AA from ruminal degradation, increasing rumen undegradable protein from 42% in SE to 68% in EP. Kinetic analysis of crude protein and AA degradation in the rumen revealed that, compared with LS and HS, EP exhibited slower rates of degradation but a shorter lag phase and a higher proportion of soluble protein. For all SBM products, the pattern of ruminal degradation, at 16 h of incubation, was characterized by extensive degradation of Lys and His, whereas Met and the branched-chain AA were degraded to the least extent. Estimates of intestinal digestibility of AA and crude protein were lower when measured in vitro than in situ; the magnitude of the difference between the 2 methods was greater (25%) with treated SBM products than with SE (10%). The availability of essential and nonessential AA was consistently greater (30%) with treated SBM than with SE. Among the treated SBM products, 4 essential AA (Ile, Leu, Phe, and Val) showed differences in availability, with values consistently lower for HS than for LS. This study showed that, based on in situ measures, heat and chemical treatment of SBM enhanced AA availability, and that compared with HS, EP and LS had a higher potential to enhance the AA supply to the small intestine of high-producing dairy cows.     

Sensory and Physicochemical Studies of Thermally Micronized Chickpea (Cicer arietinum) and Green Lentil (Lens culinaris) Flours as Binders in Low‐Fat Beef Burgers

Pulses are known to be nutritious foods but are susceptible to oxidation due to the reaction of lipoxygenase (LOX) with linolenic and linoleic acids which can lead to off flavors caused by the formation of volatile organic compounds (VOCs). Infrared micronization at 130 and 150 °C was investigated as a heat treatment to determine its effect on LOX activity and VOCs of chickpea and green lentil flour. The pulse flours were added to low‐fat beef burgers at 6% and measured for consumer acceptability and physicochemical properties. Micronization at 130 °C significantly decreased LOX activity for both flours. The lentil flour micronized at 150 °C showed a further significant decrease in LOX activity similar to that of the chickpea flour at 150 °C. The lowering of VOCs was accomplished more successfully with micronization at 130 °C for chickpea flour while micronization at 150 °C for the green lentil flour was more effective. Micronization minimally affected the characteristic fatty acid content in each flour but significantly increased omega‐3 and n‐6 fatty acids at 150 °C in burgers with lentil and chickpea flours, respectively. Burgers with green lentil flour micronized at 130 and 150 °C, and chickpea flour micronized at 150 °C were positively associated with acceptability. Micronization did not affect the shear force and cooking losses of the burgers made with both flours. Formulation of low‐fat beef burgers containing 6% micronized gluten‐free binder made from lentil and chickpea flour is possible based on favorable results for physicochemical properties and consumer acceptability.     

Ruminal metabolism, fiber, and protein digestion by lactating cows fed calcium soap or animal-vegetable fat.

Effects of two levels of Ca soap or animal-vegetable fat on digestion of fiber and N and on microbial protein synthesis were studied in five ruminally and duodenally cannulated lactating cows in a 5 x 5 Latin square. Fat was added at 0, 2.5%, or 5% of dietary DM, which consisted of a 60:40 forage:concentrate mix. Treatment did not influence DMI, duodenal OM flow, or digestibility. Fat linearly increased liquid dilution rate (12.1 vs. 11.1 h-1) and reduced liquid (53.6 vs. 62.4 L) and ruminal (61.6 vs. 70.1 L) volumes. Source and amount of fat did not influence mean ruminal pH, ammonia N, or VFA concentrations; however, animal-vegetable fat reduced acetate:propionate ratios compared with Ca soap (3.47 vs. 3.64). Neither source nor amount of fat influenced fiber flow, digestion, or efficiency of microbial protein synthesis. Source and amount of fat did not change ruminal or total digestibilities of DM, OM, ADF, or NDF; however, dietary fat increased total tract apparent digestion of N (70.3 vs. 66.8). Estimates of ruminal DM digestibility were lower (24.2 vs. 39.0) and total tract DM digestibility was higher (63.3 vs. 60.5) with Cr marker compared with C31 hydrocarbon marker. Animal-vegetable fat or Ca soap can be supplemented up to 5% of the dietary DM in high forage diets without adverse effects on ruminal metabolism and digestion.     

Estimation of the digestible energy of ruminant feedstuffs by the combined bag technique

The combined bag technique was used to estimate digestible energy of ruminant feedstuffs. Samples of corn, barley, and sorghum grains; soybean and sunflower meals; corn and wheat silages; and vetch and wheat hays were incubated in dacron bags in the rumens of dairy cattle for 3 to 72 h. Bags containing residues after 12 h of ruminal incubation were introduced into the duodenum and recovered from feces. Feeds and ruminal and intestinal residues were analyzed for dry matter (DM), organic matter (OM), crude protein (CP), neutral detergent fiber, and nonstructural carbohydrates. The effective ruminal degradability of OM was higher in grains (639 g/kg of DM) and in protein supplements (609 g/kg of DM) than in forages (373 g/kg of DM). For grains and forages, carbohydrates contributed most of the degradable OM in the rumen, but, in protein supplements, about 50% of the ruminally degradable OM originated from carbohydrate. For protein supplements, 54% of the OM that disappeared postruminally was CP, but, in the grains and forage ingredients, CP contributed less than 20% of the postruminal OM that disappeared. In grains and forages, 83% of total tract disappearance of OM was from carbohydrates. For protein supplements, CP contributed 50% to overall OM disappearance. The calculated energy equivalent of digested matter averaged among feeds was 4.71 kcal/g. A high correlation was found between digestible energy estimated by the combined bag technique and the respective National Research Council values. The combined bag technique is a useful tool for the estimation of digestible energy in feedstuffs.     

Effects of roasting on ruminal nutrient degradability of sunflower seed

A study was conducted to determine the effects of roasting sunflower seed using heated particulate medium (heated salt at 250 °C, 60 s contact of salt and sunflower seed and 120 s holding time) on crude protein (CP) fractions, ruminal dry matter (DM) and CP degradabilities, and ruminal disappearance of amino and fatty acids. Two ruminally fistulated cows were used in a randomised complete block design. Roasting of sunflower seed decreased (P < 0.05) soluble protein and increased (P < 0.05) neutral detergent‐insoluble protein with little effect on acid detergent‐insoluble protein. Results of the in situ nylon bag study showed that roasting decreased (P < 0.05) ruminal degradability of DM and CP and increased (P < 0.05) ruminal undegraded CP of sunflower seed. Roasting increased (P < 0.05) intestinal digestibility of ruminal undegraded protein. Ruminal disappearance of all amino acids (following 12 h of incubation) was greater (P < 0.05) for raw than for roasted sunflower seed. Similar results were also observed for ruminal disappearance of fatty acids. It was concluded that roasting of sunflower seed using heated salt decreased ruminal nutrient degradabilities and thus increased the concentrations of amino acids and polyunsaturated fatty acids available for digestion in the small intestine. Copyright © 2003 Society of Chemical Industry