Abstract

Two experiments were conducted to determine the effect of alkaline hydrogen peroxide (AHP) treatment (1% NaOH+1.5% H 2 O 2 ; 1 AHPMS, 2% NaOH+1.5% H 2 O 2 ; 2AHPMS) on rate and extent of degradation of mustard straw (MS) in sacco in sheep, and its in vivo digestion and ruminal fermentation characteristics when fed to sheep with concentrate (200 g per sheep daily). The treatment of straw with 1 and 2% AHP increased its sodium content by 148 and 296% to that of untreated straw (UMS). There was significant decrease in NDF and hemicellulose contents of AHP treated straw and increase in cellulose and lignin contents. Phenolic acids like ferrulic, p-coumaric and o-coumaric significantly (p<0.001) reduced by AHP treatment of mustard straw. In first experiment the in sacco degradation of DM, OM and NDF was significantly (p<0.01) greater for 2 AHPMS than for UMS at all incubation periods. The disappearance of nutrient from I AHPMS and 2 AHPMS treated straws continue to increase up to 96 h whereas in UMS the peak disappearance was found at 48 h. By using the equation {(y=a+b) (i-e - c t )} the degradation rates (c) for DM, OM, and NDF were significantly higher for UMS than AHP treated straws. Level of alkali (1 and 2%) had significant effect on degradation characteristics (a, b, c and P 0 . 0 5 ) of DM and NDF fraction of MS. However, the effect was not pronounced on OM fraction of MS. In feeding experiment, the intake of nutrients for DM, OM, cell wall constituents and energy was higher on 2 AHPMS, whereas no effect on the digestibility of these nutrients was observed. The apparent nitrogen retention was higher (p<0.05) both in 1 and 2 AHPMS groups. Water intake by animals was significantly increased due to AHP treated mustard straw feeding. Rumen liquor pH was higher in 2 AHPMS fed animals. The NH 3 -N of rumen liquor was not affected by feeding of AHP treated MS based diets. Total VFA concentration was significantly (p<0.01) higher in UMS fed group. The fractional out flow rate of DM was higher (p<0.05) in animals fed on 2 AHPMS diets compared to UMS and IAHPMS fed groups. The population of large holotrichs was higher (p<0.05) on AHP treated MS fed diets compared to UMS. The study indicated that treatment of mustard straw with AHP changed its chemical composition towards a better feed. The nutritive value of 2% AHP treated mustard straw was better in terms of dry matter intake and apparent nitrogen retention. The higher in sacco DM, OM and NDF disappearance however, was not confirmed by in vivo data in this study.

Highlights

  • Crop residues are important as livestock feed in SouthEast Asian region, and interest in their use as livestock feed is increasing as the feeds are in short supply and availability of other better quality feeds is very low (Jackson, 1977)

  • If nutritional value of mustard straw (MS) is improved through some process technology enormous quantity of roughage will be made available for ruminant livestock

  • Mishra et al 2000 following the reports from Gould, 1984; Kerley et al, 1986 and Chaudhary, 1998 and 2000, confirmed the effectiveness of alkaline hydrogen peroxide (NaOH+H2O2; Alkaline hydrogen peroxide (AHP)) to modify cell wall composition and in vitro organic matter digestibility (82-112% higher than untreated MS) of MS

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Summary

INTRODUCTION

East Asian region, and interest in their use as livestock feed is increasing as the feeds are in short supply and availability of other better quality feeds is very low (Jackson, 1977). Under a situation of inadequate availability of cereal straws for livestock feeding, there is a need to use other alternative crop residues in animal diet. The MS becomes available during the months of February to April in semi-arid region of the country. This period is considered most critical as the availability of surface vegetation and other roughage starts depleting due to harsh climatic conditions. Found in our earlier experiment (Mishra et al, 2000) and to assess feeding value of AHP treated straw in in sacco (Ørskov, 1982)

MATERIALS AND METHODS
RESULTS
AHPMS 2 AHPMS
CONCLUSIONS
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