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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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a reverse-phase column. Ether-linked PCA <strong>and</strong> FA <strong>we</strong>re calculated as the difference<br />

bet<strong>we</strong>en total <strong>and</strong> ester-linked phenolic acids. Phenolic acids <strong>and</strong> respective amounts of<br />

their different linkages <strong>and</strong> lignin types <strong>we</strong>re used in a multiple regression to select<br />

those factors explaining most of the variation in <strong>kd</strong>, 24hr <strong>and</strong> 96hr NDFD.<br />

Since most esterified PCA on lignin are not covalently attached to other cell wall<br />

polymers, they should not directly influence cell wall degradability. Ho<strong>we</strong>ver some cell<br />

wall models show how they can interfere with ferulate-lignin cross linking <strong>and</strong> in some<br />

cases reduce the proportion of lignin bound to cell wall. Figure 2 <strong>and</strong> 3 show the<br />

relationship bet<strong>we</strong>en 24hr NDFD <strong>and</strong> PCA content in NDF <strong>and</strong> ADF residues<br />

respectively. Forage groups demonstrated different relationships for digestibility from<br />

positive to negative in NDF residues. ADF residues <strong>we</strong>re instead characterized by a<br />

consistent negative relationship among all forage groups <strong>and</strong> similar results <strong>we</strong>re<br />

obtained for 96 hr NDFD.<br />

Relationship bet<strong>we</strong>en 24hr <strong>and</strong> 96hr NDFD with esterified FA content in NDF<br />

residues are shown in Figures 4 <strong>and</strong> 5, respectively. Ester-linked FA had generally a<br />

negative relationship except in bmr corn for 24hr <strong>and</strong> positive for 96hr NDFD. Ferulates<br />

primarily form as esters of arabinoxylans <strong>and</strong> later they cross-link through ether linkages<br />

with lignin. So esters of FA should not necessarily limit NDF degradation. This has<br />

probably more to do with the degree of arabinoxylans substitution.<br />

Ether linkage bet<strong>we</strong>en FA <strong>and</strong> lignin has been used a measure of cross-linking<br />

bet<strong>we</strong>en lignin <strong>and</strong> arabinoxylans <strong>and</strong> defined as the most important factor limiting<br />

energy utilization (Casler, 2001). Ho<strong>we</strong>ver in our case <strong>we</strong> <strong>we</strong>re not able to obtain<br />

consistent negative relationship with NDFD. Figure 6 <strong>and</strong> 7 show the relationship for 24<br />

<strong>and</strong> 96 hours respectively with divergent relationship for 24 hr <strong>and</strong> consistent positive<br />

ones for 96 hr NDFD. Negative effect of etherified FA on NDFD has been found in<br />

elongating internodes in maize but not in internodes that had stopped the elongation<br />

process <strong>and</strong> confirms the hypothesis that secondary cell wall development may mask<br />

the negative impact of etherified FA on NDFD. Interestingly also, bmr shows higher<br />

content of etherified FA compared to conventional corn in NDF residues, demonstrating<br />

that etherified FA is not always a good indicator of cross-linking bet<strong>we</strong>en lignin <strong>and</strong><br />

arabinoxylans <strong>and</strong> this was also shown recently by Marita et al. (2003). Ho<strong>we</strong>ver this<br />

relationship changes when ADF residues <strong>we</strong>re analyzed for ether linked FA, showing<br />

how the solubulization or branching of the lignin structure has in this case more<br />

importance than linkages. Acid detergent solution in this case might dissolve those FAs<br />

that only etherified (instead of having <strong>and</strong> ester-ether linkage).<br />

A multiple regression with stepwise selection was run within each forage group using<br />

the independent variables lignin type (<strong>ADL</strong> or Klason lignin) <strong>and</strong> their difference on an<br />

NDF basis <strong>and</strong> phenolic acids with their specific linkages also on an NDF basis. We<br />

wanted to determine how much variation in 24hr <strong>and</strong> 96hr NDFD <strong>and</strong> <strong>kd</strong> was explained<br />

by the above mentioned variables. The procedure was not able to find any significant<br />

variable for the alfalfas (P < 0.10), showing how NDF digestibility cannot be easily<br />

explained in legumes by many of these factors. All the other forage groups reached

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