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aNDF, NDFd, iNDF, ADL and kd: What have we learned?

aNDF, NDFd, iNDF, ADL and kd: What have we learned?

aNDF, NDFd, iNDF, ADL and kd: What have we learned?

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indicating where changes will most likely occur in the near future when estimating rates<br />

of digestion. This involves refinements in methodology <strong>and</strong> a more complete<br />

underst<strong>and</strong>ing of the extent of digestion.<br />

Sample Analyses<br />

Conventional <strong>and</strong> bmr corn silages, perennial ryegrasses, wheat straw, <strong>and</strong> alfalfa<br />

hays <strong>we</strong>re analyzed for fiber fractions using the procedure of Van Soest et al. (1991).<br />

Sulfuric lignin was also used as the st<strong>and</strong>ard lignin procedure (Van Soest <strong>and</strong><br />

Robertson, 1980). A small preliminary study indicated that fermentations in-situ for 16<br />

days may not be enough to reach the maximum extent of digestion <strong>and</strong> this is still being<br />

investigated. Extended fermentations <strong>we</strong>re also carried using the ANKOM in-vitro<br />

apparatus (DAISY III; ANKOM Technology Corp., Fairport, NY), because of the ease of<br />

re-inoculating the samples. This latter system allo<strong>we</strong>d a better estimation of the intrinsic<br />

<strong>iNDF</strong> of the forage after 16 days. Fermentations <strong>we</strong>re then carried for 16 days using the<br />

DAISY system <strong>and</strong> bags of polyester polyethylene terephthalate with 15 μm porosity<br />

<strong>and</strong> 8.5% open area (ANKOM Technology Corp., Fairport, NY). Jars <strong>we</strong>re re-inoculated<br />

with medium every 4 days. Fermentations in-vitro <strong>we</strong>re carried out for 6, 12, 24, 30, 36,<br />

48, 72, 96, 120, 144, 168, 192 <strong>and</strong> 216 hours, in 125 ml Erlenmeyer flasks in a 39 °C<br />

water bath under constant CO2 in Goering <strong>and</strong> Van Soest buffer (1970), <strong>and</strong> with<br />

rene<strong>we</strong>d medium after 96 hours. In-vitro flasks <strong>we</strong>re inoculated with rumen fluid from<br />

the same cows used for the DAISY fermentations, fed hay <strong>and</strong> grain. Blank samples<br />

<strong>we</strong>re run for both fermentations <strong>and</strong> used to correct for any contamination at each<br />

fermentation time. All samples at the end of the fermentations <strong>we</strong>re analyzed for NDF.<br />

Further Evaluations of Rate Estimations for NDF Digestion – Comparison to a Non-<br />

Linear Model for a First Order Approach<br />

The earliest attempts to describe the kinetics of digestion <strong>have</strong> been revie<strong>we</strong>d by<br />

Mertens (1993a, 1993b). The term ―rate of digestion‖ appeared in the 1950s, but the<br />

assessments <strong>we</strong>re mainly based on the visual interpretation of digestion curves.<br />

Waldo (1970) suggested that if the indegistible residue was subtracted, digestion of<br />

potentially digestible cell walls might follow first order kinetics. Two primary methods are<br />

used for fitting data to the first order kinetic models: linear regression on logarithmic<br />

transformations of undigested residues (ln-linear) <strong>and</strong> nonlinear estimation of<br />

parameters using multiple time points. The regression bet<strong>we</strong>en the natural logarithm of<br />

the potentially digestible NDF (pdNDF) against time results in supporting the hypothesis<br />

that pdNDF follows the first order digestion kinetics. In this case, it is critical the<br />

estimation or measurement of the indigestible fraction (<strong>iNDF</strong>) is accurate in order to<br />

accurately describe the digestion kinetics.<br />

A further problem in describing NDF digestion <strong>and</strong> kinetics is that bias can also be<br />

associated with early measurement of digestion. Usually, digestion of the pdNDF<br />

fraction does not appear to start instantaneously at time zero. Instead there is a lag<br />

period during which digestion occurs slowly or not at all (Mertens, 1993a, 1993b) while<br />

the fermentation stabilizes <strong>and</strong> bacterial attachment <strong>and</strong> enzyme synthesis has

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