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European Journal of Scientific Research - EuroJournals

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Nutritive Evaluation <strong>of</strong> Some Trees and Browse Species from Scotland 312<br />

Introduction<br />

Nutrition is perhaps the most important consideration in livestock management. The nutritive value <strong>of</strong><br />

a feed is essentially a function <strong>of</strong> the availability <strong>of</strong> its energy and nutrient contents. According to Van<br />

Soest (1983), nutritive value is multifaceted, but useful attributes <strong>of</strong> a feed are feed consumption and<br />

digestibility. Browse (shrubs and tree foliage) plays a significant role in providing fodder for ruminants<br />

in many parts <strong>of</strong> the world (Adugna et.al. 1997). Tree fodder is generally richer in protein and minerals<br />

and is used as a dry season supplement to poor quality natural pasture and or fibrous crop residues<br />

(Devendra, 1990; Kibbon and Orskov, 1993).<br />

In vitro methods for laboratory estimations and feed degradation are important tools for<br />

ruminant nutritionists. The Hohenheim in vitro gas test is extensively used for the estimation <strong>of</strong> in vivo<br />

digestibility and metabolizable energy for ruminants (Menke et al., 1979). Internationally, the gas test<br />

is <strong>of</strong> increasing interest because <strong>of</strong> the possibility <strong>of</strong> estimating the extent and rate <strong>of</strong> degradation in<br />

one sample by time series measurement <strong>of</strong> the accumulating gas volume (Blummel et al., 1990;<br />

Khazaal et al., 1993, Orskov, 2000). However, the presence <strong>of</strong> tannins and other phenolic compounds<br />

in a large number <strong>of</strong> nutritionally important shrubs and tree leave decrease their utilization as animal<br />

feed. In general, most browse species contain phenolic compounds that reduce digestibility and<br />

availability <strong>of</strong> protein, and contribute to unpalatability and reduced intake (Woodward and Reed, 1989;<br />

Kumar and Vaaithiyanaathan, 1990; Kibon and Ørskov, 1993). There have been several studies aimed<br />

at inactivating phenolic compounds using polyvinyl pyrolidone (PVP) or polyethylene glycol (PEG).<br />

Thus PEG has been used to adsorb plant phenolics during the extraction <strong>of</strong> enzymes because <strong>of</strong> its<br />

hydrophobic properties (Badran and Jones, 1965). A potential increase in in vitro (Kumar and<br />

Vaithiyanathan, 1990) and in vivo (Jones and Mangan, 1977) digestibility <strong>of</strong> tannin rich feeds by the<br />

addition <strong>of</strong> PEG-4000 has also been reported.<br />

While the nutritional potential and limitations <strong>of</strong> many tropical and Mediterranean browse<br />

species have been documented, comparatively little has been done on temperate trees species. Thus, the<br />

objective <strong>of</strong> this study was to assess the nutritive value <strong>of</strong> some tree species from Scotland based on<br />

their in vitro gas production, DM degradability in sacco and in vivo digestibility.<br />

Materials and Methods<br />

The forages used in the study were 1. Pinus sylvestris L. (Scots pine), 2. Lolium perenne L. (grass)<br />

/Trifolium repens L. (Clover) mixture, 3. Calluna vulgaris L. (Heather), 4. Picea sitchensis (Bong.)<br />

Carr. (Sitka spruce), 5. Chamaenerion angustifolium (L.) Scop. (Roseby willowherb), 6. Luzula<br />

sylvatica (Great Woodrush), 7. Pseudotsuga menziesii F. Mirb. (Douglas fir), 8. Fagus sylvatica L.<br />

(Beech), 9. Vaccinum myrtillus L. (Vaccinum), 10. Brassica oleracea (Cabbage), 11. Acer<br />

pseudoplatanus L. (Sycamore), 12. Juncus effusus L. (S<strong>of</strong>t Rush)<br />

Most <strong>of</strong> the tree leaves and browse species were hand harvested at Macaulay <strong>Research</strong><br />

Institute's experimental station at Glensaugh, Aberdeenshire, Scotland. The L. perenne was machine<br />

harvested while the B. oleracea was purchased from a local farmer. The samples were oven dried at<br />

70ºC for 48 hours and milled using a 1-mm screen.<br />

In vitro gas production<br />

In vitro gas production was measured using the method described by Blummel and Orskov (1993) by<br />

incubating the forage samples with buffer and rumen fluid and recording the volume <strong>of</strong> gas produced<br />

over time. Measurements were made after 3, 6, 12, 24, 48, 72 and 96 hours <strong>of</strong> incubation. Analysis was<br />

carried out in triplicate in the presence and absence <strong>of</strong> 200mg PEG, molecular weight 4000 (Sigma-<br />

Aldrich Company Ltd, Poole, Dorset, UK). The gas syringes were incubated by suspension from a rack<br />

fitted above a water bath. The rumen fluid was taken from two sheep, fitted with permanent rumen<br />

cannulae, receiving a diet <strong>of</strong> dried L. perenne pellets and hay.

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