No abstract

Hemodynamic changes were studied in broiler chickens during exposure to constant temperatures (10 to 35 C) or diurnal temperature cycles (10:30 C and 15:35 C), and during acute heat or cold. Packed cell volume (PCV) was significantly high at low constant temperatures (10 and 15 C), whereas at high temperatures (30 and 35 C) plasma volume (PV) was significantly high. A linear relationship between hematocrit and heart weight was observed and indicates an adaptation of heart mass to changes in cardiac output and hematocrit to meet the demands of increased basal metabolic rate. Only during the diurnal temperature cycle of 15:35 C did a significant increase in PV occur when ambient temperature (Ta) was raised form 15 to 35 C. Acute exposure of chickens to high temperature did not affect PV or PCV, but resulted in hyperthermia (44.7 +/- 0.4 C). Changes in PCV are probably related to modulation of the supply of oxygen to accommodate changes in heat production. The significant hypervolemia observed at high temperatures could occur to provide the fluid needed for heat dissipation by panting. The lack of response of the blood system to acute temperature changes may be at least partially responsible for the chickens' failure to control body temperature.

No abstract

1. In order to determine the feasibility of using high fibre diets in turkey rations, three crude fibre dietary concentrations were fed to turkey hens at three ages and performance, fibre digestibility and small intestinal morphology were determined. 2. Growth rate and feed efficiency decreased when diets contained 80 to 90 g crude fibre/kg; however, growth did not change when 60 g crude fibre/kg was fed between 1 and 4 weeks or between 6 and 8 weeks and was enhanced between 11 and 14 weeks of age. 3. Digestibilities of crude protein, fat and gross energy (GE) were depressed at fibre intakes of 80 to 90 g/kg between 1 and 4 weeks but not at later ages. Crude fibre digestibility increased with age and decreased with dietary fibre content. 4. Total small intestinal length and surface area were increased by high dietary crude fibre intake between 11 and 14 weeks. Small but inconsistent changes in the length, diameter and number of villi, villus size and area were observed in the duodenum, jejunum and ileum at the different ages as a result of feeding the different crude fibre concentrations. 5. Crude fibre can be utilised to some extent by turkeys and concentrations of 60 g fibre/kg in the diet did not result in decreased performance after 6 weeks of age.

Three series of experiments were conducted with fast-growing chickens in order: to evaluate the effects of dietary Ca and P on cholecalciferol metabolism and expression; to determine dietary Ca requirements; to determine dietary P requirements. The results of the first series confirmed previous results on the effects of dietary Ca and P on some variables of vitamin D metabolism and expression, Ca homeostasis and P metabolism in the young chicken (1-to 21-d-old), and extended them to older birds (22-to 43-d-old). The bone formation rate and the duodenal calbindin content were maintained at high levels until the age of 43 d. Dietary Ca or P restriction increased duodenal calbindin and decreased bone ash in both 22-and 43-d-old chickens, but the effect on bone ash was less pronounced in the 43-d-old birds than in the younger ones. These results suggest that: (a) the capabilities for adaptation to dietary Ca and P restriction remain high during the whole growing period; (b) the growing broilers express a high adaptive capability even when the diet contains the recommended Ca and P contents. The results of the second and third series of experiments suggest that: (c) unlike the Ca requirements of the 1-to 22-d-old chick, P requirements for growth and bone ash are similar, and are as high in the older chicks as in the younger ones (7·4-8·3 g P/kg or 4·8-5·7 g non-phytate P/kg diet); (d) although growth and bone ash in the 29-to 43-d-old chickens appear to be less sensitive to dietary Ca content, within a range close to the calculated P requirement, 10 g Ca/kg diet appears to be required for best tibia mineralization, and to a lesser extent for better growth at this age.