A method is proposed for estimating the percentage of dietary protein that is degraded by microbial action in the rumen when protein supplement is added to a specified ration. The potential degradability, p , is measured by incubating the supplement in artificial-fibre bags in the rumen and is related to incubation time, t , by the equation p = a+b (1 – e -ct ). The rate constant k , measuring the passage of the supplement from the rumen to the abomasum, is obtained in a separate experiment in which the supplement is combined with a chromium marker which renders it completely indigestible. The effective percentage degradation, p , of the supplement, allowing for rate of passage, is shown to be p = a +[ bc/(c+k) ] (1- e -(e+k)t ) by time, t , after feeding. As t increases, this tends to the asymptotic value a+bc /( c+k ), which therefore provides an estimate of the degradability of the protein supplement under the specified feeding conditions. The method is illustrated by results obtained with soya-bean meal fed as a supplement to a dried-grass diet for sheep. The incubation measurements showed that 89% of the soya-bean protein disappeared within 24 h and indicated that it was all ultimately degradable with this diet. When the dried grass was given at a restricted level of feeding the allowance for time of retention in the rumen reduced the estimate of final degradability to 71% (69% within 24 h). With ad libitum feeding there was a faster rate of passage and the final degradability was estimated to be 66% (65% within 24 h).

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The estimation of protein degradability in the rumen from incubation measurements weighted according to rate of passage

The Cornell Net Carbohydrate and Protein System (CNCPS) has a submodel that predicts rates of feedstuff degradation in the rumen, the passage of undegraded feed to the lower gut, and the amount of ME and protein that is available to the animal. In the CNCPS, structural carbohydrate (SC) and nonstructural carbohydrate (NSC) are estimated from sequential NDF analyses of the feed. Data from the literature are used to predict fractional rates of SC and NSC degradation. Crude protein is partitioned into five fractions. Fraction A is NPN, which is trichloroacetic (TCA) acid-soluble N. Unavailable or protein bound to cell wall (Fraction C) is derived from acid detergent insoluble nitrogen (ADIP), and slowly degraded true protein (Fraction B3) is neutral detergent insoluble nitrogen (NDIP) minus Fraction C. Rapidly degraded true protein (Fraction B1) is TCA-precipitable protein from the buffer-soluble protein minus NPN. True protein with an intermediate degradation rate (Fraction B2) is the remaining N. Protein degradation rates are estimated by an in vitro procedure that uses Streptomyces griseus protease, and a curve-peeling technique is used to identify rates for each fraction. The amount of carbohydrate or N that is digested in the rumen is determined by the relative rates of degradation and passage. Ruminal passage rates are a function of DMI, particle size, bulk density, and the type of feed that is consumed (e.g., forage vs cereal grain).

A net carbohydrate and protein system for evaluating cattle diets: II. Carbohydrate and protein availability.

A theoretically-based model for predicting total digestible nutrient values of forages and concentrates

Chemical factors involved in ruminal fiber digestion.

Influence of hydrogen on rumen methane formation and fermentation balances through microbial growth kinetics and fermentation thermodynamics

A new liquid marker, cobalt-ethylenediamine tetraacetic acid (EDTA), and two solid markers, chromium (Cr) and cerium (Ce) mordanted plant cell walls, were investigated. Synthesis and methods of analysis are described for the markers. The Cr- and Ce-cell wall complexes were tested for stability to EDTA, hydrochloric acid and rumen microorganisms. Plant cell walls were rendered indigestible by mordanting with Cr and 98% of the marker remained on the fibre after a simulated sequence (in vitro) of digestion. Ce-mordanted cell walls were 35% digestible in vitro using a rumen culture, and 56% of the marker could be washed off the remaining fibre. Treatment with EDTA removed all Ce and 15% of the Cr. Hydrochloric acid (0.01M) had a negligible effect on the removal of Cr from the cell walls, whereas 0.1M acid removed, on average, 10% of the marker. Losses of Cr from the mordant may be related to the quality of the preparation. Co-EDTA was found to be comparable to Cr-EDTA. The urinary excretion of Cr and Co was 2–3% in most animals except in rabbits, which excreted as much as 30% of the liquid markers in the urine.

P E Colucci

Papers

Investigation of chromium, cerium and cobalt as markers in digesta. Rate of passage studies

Feed Intake, Apparent Diet Digestibility, and Rate of Particulate Passage in Dairy Cattle

Investigation of chromium, cerium and cobalt as markers in digesta [of ruminants, horses and rabbits]. Rate of passage studies.