A mathematical representation of the energy-requiring processes of protein turnover and Na+,K+-transport in the tissues of growing lambs is described. This model was then used to examine the relative contributions of these processes to ATP expenditure at two different growth rates (90-230 g/d). Protein turnover accounted for 19% of whole-body ATP expenditure at both growth rates examined, with the gastrointestinal tract (GIT), accounting for 25-27%, muscle for 21-26%, skin for 23-26% and liver for 13% of total protein turnover energy costs. The contribution of Na+,K+-transport increased from 18 to 23% of whole-body heat production as growth rate increased, with the GIT accounting for 39 and 50%, muscle for 17 and 10% and liver for 18 and 23% of total Na+,K+-transport costs at low and high nutrient inputs, respectively. Thus, protein turnover accounted for 19% of the increment in ATP expenditure due to the increased nutrient input at the higher rate of growth, while Na+,K+-transport accounted for 39%, and fat turnover and accretion accounted for 25%, leaving 17% of the ATP increment unaccounted for.

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Animals exhibit a first priority, or threshold, energy requirement that must be met from dietary intake before there will be a yield of products. When fasted, rested and held in a thermoneutral environment, animals exhibit a basal level of energy expenditure that is supported by oxidation of substrates, principally lipids and amino acids, mobilized from body tissues. It is widely presumed that the maintenance energy requirement is the dietary metabolizable energy (ME) required to meet this first-call basal metabolic rate plus the energy needed to support minimal activity and urinary energy excretion (Agricultural Research Council, 1980); that is maintenance ME provides for energy balance under confined conditions. Questions that immediately arise are: what are the metabolic components of maintenance energy expenditure, what are their quantitative roles, is energy balance achieved by simply meeting basal energy expenditure and do the metabolic components of basal metabolism change with level of intake? These questions will be addressed in the present paper.

We investigate the growth of periodically aligned silicon microstructures for the fabrication of square spiral photonic crystals using the glancing angle deposition phi-sweep process. We report the optimization of the phi-sweep offset angle for fabrication of microstructures with more precise geometry. The effects of varying the sweep offset angle of the phi-sweep process are studied for films deposited onto a square lattice array of growth seeds. To represent one growth segment of the phi-sweep process, we fabricate 15 nm silicon thin films using several azimuthal substrate offsets from 0° to 45° at a vapor incidence angle of 85°. We also deposit silicon square spirals on square lattice arrays with the phi-sweep method, using various sweep offset angles from γ = 0° to 45°. We find that using an offset angle of γ = 26.5° optimizes the shadowing geometry, which minimizes anisotropic broadening, producing greater quality photonic crystal structures. From normal incidence reflection spectroscopy, a maximum full width at half-maximum of 273 ± 3 nm and a relative peak width (Δλ/λ) of 16.1 ± 0.1% were found for a sweep offset angle of γ = 26.5°.

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