Effect of dietary inclusion of ascorbic acid and palm oil on the performance of laying hens in a hot tropical environment

1. Two experiments were conducted to evaluate the effects of including ascorbic acid (AA), palm oil or a combination of both in the diets of laying hens during the hot months in a tropical environment.

2. The inclusion of AA improved egg production, food intake and efficiency of utilisation, and decreased the cost of food per kg egg. The addition of 400 mg AA/kg diet gave the most efficient performance.

3. Palm oil inclusion reduced the effect of heat stress and increased egg production, egg weight, food intake and efficiency of utilisation.

4. When 200 mg AA and 50 g palm oil/kg were used, additive responses were obtained with further improvements in egg production, food cost and efficiency.

5. Ascorbic acid and palm oil when fed alone or in combination reduced the incidence of cracked eggs.

6. Thus, 400 mg ascorbic acid/kg of diet, 50 g palm oil or 200 mg AA plus 50 g palm oil/kg diet ameliorated the effects of heat stress in laying hens.     

Contribution of lipoprotein lipase activity to the differential growth of three adipose tissue depots in young broiler chickens

1. The growth of three distinct adipose tissue depots around the abdomen, neck and thigh was measured in a commercial strain of broiler, and related to the changes in activity of lipoprotein lipase within each depot.

2. At 10 d of age there was no significant difference between the weights of the depots. Thereafter the abdominal fat pad exhibited a much greater rate of growth than the other two depots so that by 55 d of age the abdominal fat pad was 4 times the size of the leg depot and 3.4 times the size of the neck depot.

3. Changes in total lipoprotein lipase activity for all three depots showed a similar pattern to the changes in their weight.

4. When [¹⁴C]‐VLDL was injected intravenously into birds at 15 and 57 d of age the percentage taken up into the abdominal fat pad was greater than that into the other two depots at both ages. At 57 d of age the abdominal fat pad had a 2.3‐fold greater uptake than at 15 d whereas the other two depots showed no significant differences at the two ages.

5. These results provide further evidence for a key role of lipoprotein lipase in regulating adipose tissue growth in broilers. They also demonstrate that although the abdominal fat pad has been used in a number of studies of adipose tissue metabolism it is not necessarily representative of other depots.     

Effects of triazole fungicides on sterol biosynthesis during spore germination of Botrytis cinerea,Venturia inaequalis and Puccinia graminis f. sp. tritici

With three plant pathogens,Botrytis cinerea, Venturia inaequalis and Puccinia graminis f. sp.tritici, the time course of sterol biosynthesis during spore germination was examined by labeling experiments along with the question whether this pathway could be inhibited by triazole fungicides. Conidia ofB. cinerea andV. inaequalis are able to synthesize sterols immediately after the beginning of the germination process when the germ tubes have not yet emerged. On the contrary uredospores ofP. graminis start sterol biosynthesis after 6 to 8 h germination time almost at the end of the germ tube phase, indicating that sterol reserves of the spores are likely to be used for the germ tube growth.The sterol C-14 demethylation appeared to be the rate limiting step within the sterol biosynthetic pathway: the half life of 24-methylenedihydrolanosterol was less than 1 h forB. cinerea. It was more than 1 h forV. inaequalis and 3 h forP. graminis. Independent of these differences in the time course of sterol biosynthesis and in the C-14 demethylation rate, the synthesis of sterols in germinating spores was strongly inhibited by triazole fungicides in all three pathogens examined. In contrast toP. graminis, this inhibition could be demonstrated withB. cinerea andV. inaequalis even in ungerminated conidia, indicating that the fungicides were rapidly taken up and reached their target within 1 or 2 h. These results are discussed along with the question whether spore germination can be used as a bioassay for the estimation of sensitivities of triazole fungicides.