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Twenty-seven Holstein cows were fed total mixed rations (TMR) supplemented with protected palm fat (PPF), rapeseed cake (RC) or extruded soyabean (ESB) for 14 weeks. Feed intake and milk yield were recorded. Samples of milk were taken weekly and analysed. Jugular blood was taken three times two hours after feeding. Cows of the PPF group consumed significantly less feed and produced more milk than cows of the RC and ESB groups (32.9, 31.7 and 30.7 kg fat-corrected milk/d, respectively). Milk fat from cows fed diets supplemented with RC and ESB contained more stearic, vaccenic and conjugated linoleic acids, and less palmitic acid than milk fat of cows fed the PPF diet (P<0.05). The content of polyunsaturated fatty acids (PUFA) in milk fat of cows fed ESB was higher, and the atherogenicity of its fatty acids, lower than in milk fat of other cows. This was, however, accompanied by lower oxidative stability of milk fat. Supplementation of TMR with RC increased the spreadability index of manufactured butter (P<0.025). Both milk and blood urea concentrations were significantly lower for cows fed the ESB diet. This suggests that crude protein in this diet was less degradable than in other diets. Body weights of cows on diets RC and ESB increased by 11.3 and 15.6 kg, respectively, whereas the body weight of cows on the PPF diet decreased by 1.7 kg, on average. It can be concluded that feeding oilseed-based supplements to dairy cows decreased milk yield and milk production efficiency somewhat, but improved the nutritional quality of milk fat.
The intestinal and total tract digestibilities of phosphorus (P) and phytate P were determined in digestibility trials with laying hens and broiler breeders fed a diet containing P, phytate P and Ca at 6.37, 2.00 and 34.1 g·kg-1, respectively. In both digestibility trials, the total tract digestibility of phytate P was higher than the intestinal digestibility (33 and 35% vs 20 and 18%). In contrast, in both trials the total tract retention of P was lower than the intestinal retention (22 and 19% vs 52 and 42%). Phytate P represented 29.2% of the excreta P of laying hens and 23.6% of the excreta P of broiler breeders. The corresponding proportions of phosphate P were 48.7 and 46.6%, respectively. Samples of digesta and small intestinal mucosa of laying hens were diluted with physiological saline containing sodium phytate and incubated in vitro to determine the phytase activity. The average specific phytase activities in the crop, stomach, small intestinal contents, mucosa and caecal contents were 10.2, 9.2, 14.6, 11.5 and 135 μmol·h-1·g-1, respectively. The total phytase activities (per segment) in the small intestine (including the mucosa) and the caeca were 586 and 663 μmol·h-1, respectively. It can be concluded that phytase activity was present in all sections of the digestive tract. Consequently, in hens fed a wheat-maize-soyabean diet without a phytase supplement, phytate P was partially digestible. A part of the phytate degradation occurred in the hindgut.
Two hundred and forty hens were assigned to six dietary treatments and fed a maize-wheat-soyabean diet supplemented per kg with 0, 150, 350, 550, 750 and 950 mg of marigold flower extract (MFE) containing lutein and zeaxanthin in the amount of 21.26 and 9.65 mg · kg–1 , respectively. There was observed no MFE addition effect on hens body weight and feed conversion ratio. The higher hen-day egg production was stated for group fed diet supplemented with 550 and 950 mg of MFE per kg of diet, whereas egg weight was increased in groups fed 550 and 750 mg MFE per kg of diet. The treatment effects on the albumen parameters, and yolk and shell percentages were not statistically significant. Dietary MFE addition increased the yolk colour score (DSM Yolk Colour Fan), and redness and yellowness of the yolks but decreased their lightness. Supplementation of MFE increased the lutein and zeaxanthin concentration in the egg yolks in a dose-dependent manner, from 12.34 and 5.92 mg · kg–1 dry matter (control) to 36.33 and 25.59 mg · kg–1 dry matter (group fed diet with 950 mg MFE per kg), respectively. No treatment effect on the concentrations of retinol and α-tocopherol in the yolk was observed. Dietary MFE significantly increased the oxidative stability of eggs lipids stored at 18 °C for 28 days. It can be concluded that 1. hen diet supplementation with MFE provides the yolk pigmentation required by consumers, and 2. MFE (in the amount of 550 mg · kg diet) is a suitable alternative to commercial synthetic xanthophylls.
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