A model of a ley farming system with particular reference to sub model for animal production.

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dc.contributor Arnold, GW
dc.contributor Campbell, NA
dc.date.accessioned 2012-01-25T12:20:22Z
dc.date.available 2012-01-25T12:20:22Z
dc.date.issued 1972
dc.identifier.citation Proc. Aust. Soc. Anim. Prod. (1972) 9: 23-30
dc.identifier.uri http://livestocklibrary.com.au/handle/1234/6598
dc.description.abstract Proc. Aust. Soc. Anim. Prod. (1972) 9: 23 A MODEL OF A LEY FARMING SYSTEM, WITH PARTICULAR REFERENCE TO A SUB-MODEL FOR ANIMAL PRODUCTION G. W. ARNOLD and N. A. CAMPBELL* Summary The structure of a model of a ley farming system in a Mediterranean environment is briefly described. A sub-model for predicting liveweight changes and wool production of Merino wethers grazing annual grass-clover pastures is described in detail. Predicted liveweights were within 5 per cent of actual liveweights for most of the year on pastures varying widely in botanical composition and grazed at either a high or low stocking rate. Predicted wool production was within 15 per cent of actual values. Problems in obtaining data for the model functions, and the value of the model are discussed briefly. I . 1NTRODUCTION Much research has been, and currently is being, carried out on many facets of the production of crops, pastures and animals in Mediterranean environments. However, when we attempted to integrate the available information into a study of the whole ley farming system, we found that there was insufficient information available to structure the processes involved. Our objective in modelling the ley farming system is to highlight strengths and weaknesses of our present knowledge of the system, and provide a basis for planning future research more effectively. A word picture of the overall system was constructed using a similar structure and terminology to that proposed by Van Dyne (1970) for the Grassland Bsiome model. Crop and pasture variables include pools of seed, green vegetative mass and dead material. Animal variables include numbers in different age and sex classes and animal type, the mean weight per animal in each class, and, for sheep, the mean weight of fleece per animal. Driving forces are rainfall, temperature and radiant energy. The model also contains the physical processes such as cultivation for, and harvesting of crops, and the effects of marketing of products. A simplified visual picture is shown in Figure 1. The overall model was then considered as a series of sub-models, each describing a different component of the system. The sub-models are crop growth, cultivation, pasture growth, animal liveweight change and wool growth and animal numbers (reproduction). These are designed to be readily interfaced within the structure of the overall model, so that different components can be developed separately, and modified versions of these component sub-models can be ,included, when necessary, without affecting the remaining structure of the model. i-CSIRO, Division of Plant Industry, Private Bag, P.O. Wembley, Western Australia, 6014. +CSIRO, Division of Mathematical Statistics, Private Bag, P.O. Wembley, Western Australia, 6014. It was decided to develop the animal Iiveweight change and wool growth sub-model initially, as input-output data was available for validation of the submodel after it was built, and the extent of knowledge of the processes involved was more detailed than for the other sub-models. II. ANIMAL GROWTH SUB-MODEL (a) Liveweight change The model predicts the daily liveweight of medium Peppin Merino wethers grazing annual pasture containing any proportions of Bromus mollis and TrifoZium subterraneum. The validation is on original data, from a grazing experiment, some of which have been published by Davies et al. (1966) and Greenwood et al. (1968). Sequential values for available pasture dry matter were measured at three weekly intervals, and daily figures determined by interpolation. The relationships described below were derived from the relevant literature and from data collected at the W.A. Laboratories, and converted into mathematical functions. A more detailed write up and a computer listing is available on request. Digestible organic matter intake is assumed to be a function of liveweight, 'available' pasture and the digestibility of the pasture on offer, with maintenance requirement a function of 'available' pasture and Iiveweight. The resulting energy surplus or deficit is then converted to tissue gain or loss. This summary is expanded below, with equations of the model given in Table 1. The diet selected by the grazing animal is a function of the quantity and quality of plant material on offer. The amount of green material relative to the total dry matter of the pasture is taken as the major determinant of diet quality, because the animal will select heavily for green material in preference to dry whenever possible. The per cent green herbage in the diet (PGD) is a function of per cent green herbage in the pasture (PGP) and total dry matter (TDM) present - equation 1. Arnold et aZ. (1966) found that even on low pasture availability (less than 500 k/ha) the diet contained less than 4 per cent of dry herbage, although the pasture contained up to 40 per cent. Because of this selectivity by the animals, TDM is adjusted for the amount of green material the animal selects (given by PGD) to give the 'available' dry matter (ADM) which determines intake - equation 2. When the pasture is dry, ADM is taken as simply TDM. The maximum potential organic matter intake of all herbage (OMI-g/day) is initially a function of Iiveweight (LWT) - equation 3, based on Allden (1968) and Arnold et al, (1964), and is then adjusted for 'available' dry matter and pasture composition. Species with erect growth habits, such as grasses, sustain higher intakes at low availabilities than species with prostrate growth habits such as clover; Greenwood and Davies (unpublished); Smith and Biddiscombe (unpublished); and Arnold and Dudzinski (1967a, b). Thus the function relating OMI and ADM is adjusted for the per cent grass in the diet, which is assumed to be the per cent grass in the green herbage (PGR) equation 4. Since it is assumed that the sheep eat grass and clover (both green and dry) in proportion to the amounts of each present (if digestibility is non-limiting) the 25 TABLE 1 ADM DCL DGR DME DRM ECV GRM LWT OMC OMG OMI PGD PGP PGR PNC TDM WLG Available dry matter Digestible clover Digestible grass Animal maintenance requirement Dry material on offer Energy conversion Green material on offer Liveweight Organic matter intake of clover Organic matter intake of grass Organic matter intake Per cent green herbage in diet Per cent green herbage in pasture Per cent grass in the green herbage Per cent nitrogen content Total dry matter Wool growth 26 organic matter intakes of grass (OMG) and clover (OMC) are given by: OMG = OMI * PGR OMC = OMI * (1 - PGR) Organic matter intake is then adjusted for the digestibility of the grass and clover, using data published by Ulyatt et al. (1967); Osbourn et al. (1966) and Conrad (1966). The slope of the curves appears to be similar for most temperate species but the position appears to change - equations 5 and 6. Digestibilities and nitrogen contents of the four fractions viz.: green (DGG) and dry (DDG) grass, and green (DGC) and dry (DDC) clover are read in. Digestible organic matter intake (DOM) is then calculated from the organic intakes and digestibilities: Digestible organic matter for animal maintenance requirement (DME) (equation 7) is determined as a function of pasture availability, derived from results of Graham ( 1966). The energy gain or loss of the animal (EGL) is simply the difference between DOM and DME. If there is a surplus of energy, this is converted to tissue, the energy value (ECV) (equation 8) of which is taken as a linear function of liveweight comparable to that of Searle and Graham ( 1970). If there is a deficit of energy for maintenance, the energy obtained from tissue catabolism, is given by dividing ECV by 1.8 (from Figure 5, Graham 1969). The liveweight change (LWC) is then given by: (b) Wool growth Wool growth (WLG) has a maximum potential of 20 g clean wool/sheep/ day. This value is then adjusted according to energy intake (equation 9 - based on Pattie and Williams ( 1967) ) and for nitrogen content of the diet (PNC) (equation 10- adapted from Piper and Dolling ( 1969) ), the latter being determined in a similar way to digestibility. Agreement between simulated and actual liveweights for all sets of data (two stocking rates by three nitrogen levels) is within 5 per cent for most of the year for sheep grazing pastures ranging from grass to clover dominance. Figure 2 shows the results for either grass or clover dominant pastures only. Although wool growth was simulated daily, the seasonal changes in wool growth were not measured in the experiment. Predicted weights of clean wool at shearing were from 0 to 15 per cent higher than actual weights (see Figure 2). The effect on Iiveweight of changing parameter values was examined for most functions. Greatest sensitivity was to changes in equations 4 to 6 and 8. The effect of putting the grass parameter values for clover in equation 6 is shown in Figure 2a, c. The results are encouraging since the evidence on differences in intake, digestion and metabolism of clover and grass diets, and on selection by animals between them is inadequately quantified for modelling. Also, there is little information on wool growth in relation to energy intake. To, test the model more stringently, a validation experiment is in progress, in which detailed measurements of inputs and animal responses are taken fortnightly to obtain model 'throughputs'. Until this information is available there seems 27 (c) Validation 28 29 little value in attempting to obtain a closer agreement between the actual and predicted liveweights as we do not know in what area(s) the sub-model is deficient. (d) Problems and value Little information is available to define accurately many of the functions because most studies are limited to responses of animals for only one, two or three levels of an input, or to part of the annual cycle in 'ecosystem' studies. This sub-model was not constructed to give predictions of sheep liveweight independently. Its value for this purpose will depend on whether the parameter values of the functions differ markedly for different environments, and this cannot be tested unless there -are precise input data. In the future, these inputs will be provided from the pasture growth sub-model. Once a successful model has been developed it can be used to study the effects of various management techniques on the production of ley farming systems and to predict the likely production of various aspects of the farming system in different seasons. III. ACKNOWLEDGMENTS The authors were ably assisted by Messrs. R. J. W. Barron, K. A. Galbraith and Mrs. A. Pennock. IV. REFERENCES Allden, W. G. (1968). Australian Journal of Agricultural Research, 19: 621. Arnold, G. W., McManus, W. R., and Bush, I. G. (1964). Australian Journal of Experimental Arnold, G. W., Ball, Judith, McManus, W. R., and Bush, I. G. (1966). Australian Journal of Arnold, 18: Arnold, 18: Conrad, Davies, Agricultural Research, 17: 543. Agriculture and Animal Husbandry, 4: 392. G. W., and Dudzinski, M. L. (1967a). Australian Journal of Agricultural Research, 349. G. W., and Dudzinski, M. L. (196%). Australian Journal of Agricultural Research, 657. H. R. (1966). Journal of Animal Science, 25: 227. H. L., Greenwood, E. A. N., and Watson, E. R. (1966). Proceedings of the Australian Graham, N. McC. (1966). Australian Journal of Agricultural Research, 18= 127. Graham, N. McC. (1969). Australian Journal of Agricultural Research, 20: 375. Greenwood, E. A. N., Davies, H. L., and Watson, E. R. (1966). Australian Journal of Agricultural Research, 18: 447. Osbourn, D. F., Thomson, D. J., and Terry, R. A. (1966). Proceedings of the Tenth ZnterPattie, W. A., and Williams, A. J. (1967). Australian Journal of Experimental Agriculture and Animal Husbandry, 7: 117. Piper, L. R., and Dolling, C. H. S. (1969). Australian Journal of Agricultural Research, 20: 561. Searle, T. W., and Graham, N. McC. (1970). Proceedings of the Australian Society of Animal Ulyatt, M. J., Blaxter, IS. L., and McDonald, I. (1967). Animal Production, 9: 463. Van Dyne, G. M. (1970). 'The Grassland Ecosystem' (Ed. R. L. Dix and R. G. Beidleman). (Colorado State University: Colorado). Production, 8: 472. national Grassland Congress, Helsinki, 3 63. Society of Animal Production, 6: 222. 30'
dc.publisher ASAP
dc.source.uri http://www.asap.asn.au/livestocklibrary/1972/Arnold72.PDF
dc.title A model of a ley farming system with particular reference to sub model for animal production.
dc.type Research
dc.identifier.volume 9
dc.identifier.page 23-30


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