School of Agriculture, Food and Ecosystem Sciences - Theses

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    The ecology and physiology of two species of Carduus as weeds of pastures in Victoria
    Parsons, William Thomas ( 1977)
    Slender thistles (Carduus pycnocephalus and C. tenuiflorus) were introduced to Australia about the 1880s. They are now important weeds of pastures in much of southern Australia and are difficult to control with present methods. This study was undertaken to investigate several aspects of the ecology and physiology of the plants with the belief that a knowledge of some of these aspects, particularly of seed germination and seedling establishment, might disclose some "weakness" in the plants' growth which could be exploited to improve control measures. Because of confusion over differences between the two species which occur in Australia the initial step was to evaluate the morphological features which have been used to distinguish between the two species. Although they are very similar morphologically, cytological evidence confirmed that the two species were quite distinct and, in fact, had quite different evolutionary origins. Germination of seeds of slender thistles is controlled by three separate forms of dormancy; these are known as innate, induced and enforced dormancy. Dormancy ensures that the plants will survive in a Mediterranean-type climate and also colonize areas with quite different climates and, most importantly, survive natural catastrophes such as drought, fire, and flood. The germination of slender thistles in the field is confined to a very short period (about 6 weeks) after the autumn break in any year. This is a "weakness" in the plants' survival mechanism because they are vulnerable in that year, at least, to any treatment which can kill seedlings. The herbicide, diquat, was found to kill young seedlings of slender thistles and not affect seedlings of desirable pasture plants associated with the thistles in southern Australia. This treatment is economical and leads not only to a reduction in thistles but an increase of about 30% in pasture production. Several other aspects of the plants' growth were investigated. Slender thistles have early growth characters which give them advantages over more desirable components of pastures. They are more competitive than subterranean clover and ryegrass over a wide range of levels of nutrients, and the traditional approach to pasture improvement in southern Australia of applying superphosphate and sowing subterranean clover will encourage, not suppress, slender thistles. Since grazing animals generally do not eat slender thistles the presence of thistles in pastures at densities commonly occurring in Victoria considerably reduces pasture production.
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    Effects of growth patterns on body composition and compensatory growth in sheep
    Hogg, Barry William ( 1977)
    The literature related to compensatory growth in ruminants, with particular reference to sheep, has been reviewed. An experiment was conducted which examined the effects of planned BW losses on growth rate, body composition, wool growth and nitrogen and energy utilisation of sheep when ad libitum feeding was resumed. Sheep were fed a pelleted ration throughout the experiment, and BW loss induced by reducing feed intake. Following developmental growth from 30 to 37.8 kg, Groups B and C lost 21% BW at 122 and 63 gd-1, respectively to reach 30.2 kg BW. Following developmental growth from 30 to 46.7 kg (Groups D and E), Group D lost 34% BW at 125 gd-1 to reach 30.8.kg BW, while Group E lost 23% BW at 157 gd-1 to reach 35.0 kg. Group A was a control group fed ad libitum throughout the experiment. When ad libitum feeding was resumed compensatory growth occurred in treatment groups for up to 10 kg recovery of BW. Group D showed the most persistent increases in growth rate compared with that of control sheep, however, above 50 kg BW there were no significant differences between groups in growth rate. Weight loss did not produce a reversal of the compositional changes which occurred with increasing BW during developmental growth, in the whole body, carcass or offal. However, differences in composition between groups at the end of weight loss were not significant. During compensatory growth there were few differences between groups in the relative growth rates of protein, fat, ash or water in the whole body, carcass or offal. There were some differences between groups in weights of components at specific BW, carcass weight (CW) and offal weight WW), most notably fat and ash. However, these differences appeared to be transitory, and reflected the composition of that portion of the animal at the start of realimentation, rather than an effect of weight loss which was maintained during compensatory growth. The body, carcass and offal composition of sheep appeared to be resilient to periods of nutritional stress, and tended to return to the "normal" composition expected at that weight. The effects of up to 18 weeks severe undernutrition, resulting in rapid BW loss, were able to be overcome during compensatory growth when feed was offered ad libitum. Compared with developmental growth, nitrogen retention increased during compensatory growth. However, the efficiency of ME utilization was not different during these two periods of growth, although DE requirements for maintenance were lower during compensatory growth, compared with developmental growth. Dry matter intakes (DMI) of treatment groups required up to 13 weeks to return to the DMI of sheep during developmental growth, once ad libitum feeding was resumed. Over their respective growth paths Groups A, B, C, D and E required the same amount of feed to reach 50 kg BW. Wool growth rate (WGR) responded more slowly than BW to changes in level of nutrition, both during weight loss and during compensatory growth. There was a lag phase of at least 30 days. WGR during compensatory growth was reduced and required up to 14 weeks to return to developmental WGR after ad libitum feeding was resumed. Total body water (TBW), estimated from tritiated water (TOH) space in sheep undergoing compensatory growth, was overestimated by at least 20%. TOH space was measured without imposing a period of prior starvation on the sheep, and this may have contributed to the large overestimate. Multiple regression equations including TOH space, BW and a maturity factor (M), were able to explain up to 95% of the variation in chemical composition of the body, but residual standard errors were still high.