Subacute ruminal acidosis (SARA) was induced by replacing 25% of the total mixed ration intake [dry matter (DM) basis] with pellets consisting of 50% wheat and 50% barley. This reduced dietary forage content (DM basis) from 39.7 to 29.8% and increased the dietary concentrate content from 60.3 to 70.2%. Induction of SARA reduced the 24- and 48-h in situ neutral detergent fiber (NDF) degradabilities of grass hay numerically from 31.5% to 24.6% (P = 0.29) and from 51.3% to 36.9% (P < 0.05), respectively. The 24- and 48-h in situ NDF degradabilities of legume hay were reduced from 35.3 to 26.3% (P < 0.05) and from 49.0 to 35.8% (P < 0.05), respectively. The 24- and 48-h in situ NDF degradabilities of corn silage were reduced from 44.0 to 37.2% (P < 0.05) and from 56.1 to 44.8% (P < 0.05), respectively. This study suggests that induction of SARA by excess feeding of wheat/barley pellets reduces the rumen digestion of NDF from grass hay, legume hay, and corn silage.
Two hundred and forty Hubbard X Hubbard broiler breeders at 19 weeks of age were weight-sorted and transferred to individual laying cages where one of six experimental diets was provided to 41 weeks of age. Each diet was represented by 10 replicate groups of 4 individually caged and fed birds. Feed allocation was gradually increased to 150 g/bird per day, which provided 19 or 25 g crude protein and either 325, 385, or 450 kcal metabolizable energy (ME)/bird per day. Hens were inseminated every 7 days with .05 ml pooled semen from Hubbard males. Hen-day production was 1.6% lower with the high vs. low protein intake. Peak egg production occurred at 31 weeks and was 77.3, 87.9, and 84.1% for the low (L), medium (M), and high energy (H) intakes, respectively (P less than or equal to .01). Egg weight increased as the protein or energy intake increased; yolk content increased as energy intake increased or as broiler breeders aged (P less than or equal to .01). Carcass fat, protein, and moisture content of defeathered 41-week-old breeders were L: 45.5, 44.4, 56.6; M: 49.0, 40.4, 54.8; and H: 58.4, 32.5, 50.4, respectively (P less than or equal to .01). There were no dietary effects on hatchability, embryonic mortality, or fertility. From 32 to 35 weeks of age the higher protein intake increased egg weight by 1.2 g (P less than or equal to .05) and chick weight by .6 g; whereas hatched live chick weight was 39.6, 39.7, and 41.0, for L, M, and H diets, respectively (P less than or equal to .05).(ABSTRACT TRUNCATED AT 250 WORDS)
This experiment determined the effects of dietary protein solubility on amount, form, and route of nitrogen loss in lactating Holstein dairy cows, and the ability of the Cornell Net Carbohydrate and Protein System (CNCPS) to accurately predict rumen microbial yield, serum urea N (SUN), milk urea N (MUN), and fecal N. Eighteen multiparous Holstein cows were assigned randomly to one of three dietary treatments that were similar in crude protein (17.7%) content but differed in their content of soluble intake protein (SIP). Dietary contents of SIP, as % of total CP were 30, 36, and 48%. The experimental period was 21 d, and total N balance collections were done during the last 5 d. As dietary content of SIP increased, excretion of urinary N increased quadratically, and it was the primary route of N excretion. Urinary excretion of purine derivatives (PD) responded quadratically as dietary SIP content increased. The CNCPS predicted a quadratic decrease in total metabolizable protein (MP) supply. No effect of dietary content of SIP was detected on MUN and SUN. The CNCPS predicted a quadratic decrease in SUN and MUN as dietary SIP increased. Results from this study indicated that changing the dietary content of SIP altered routes of N excretion in dairy cows, but had no effect on total N balance. The CNCPS did not adequately predict changes in SUN and MUN for cows fed diets varying in SIP.
The objective of this study was to evaluate the effect of feeding prepubertal heifers a diet containing a high level of polyunsaturated fatty acids on mammary development and milk production. A total of 116 Holstein heifers were either fed a conventionally formulated concentrate or a high oil (HO) concentrate, using the same formulation but including 20% soybean oil, from birth to 6 mo of age. After 6 mo of age, all heifers were managed identically. Mammary gland development was evaluated on heifers slaughtered at 4 mo (n = 10) and 12 mo (n = 30) of age. Other heifers were bred when they reached 15 mo of age and milk production and feed intake were recorded every day from wk 4 to 18 of lactation. Feeding the high oil concentrate increased the concentration of linoleic acid in blood plasma (176%) and mammary fat pad (78%) at 4 mo of age and mammary fat pad (93%) at 12 mo of age. At 4 mo of age, mammary development was similar in both treatments. At 12 mo of age, total, parenchyma, and stroma weights of the mammary gland were not affected by treatments. However, lipid content was lower and concentration of DNA was higher in the parenchyma of heifers fed the high oil diet. Nevertheless, total parenchymal DNA and dry fat free tissue content did not reach statistical significance despite the fact that they were, respectively, 15 and 21% higher in HO heifers. Milk production and composition was not affected by treatments. In conclusion, feeding prepubertal heifers with a high oil concentrate slightly improved the mammary development but effects were too small to be translated into better lactating performances.
The partitioning of AME intake (MEI) and recovered energy (RE; defined as MEI minus heat production) was investigated on Hubbard broiler-breeder hens (BB) by using indirect calorimetry and energy balance. The regression of RE on MEI was linear (R2 = .96; P less than .01) with a slope of .817 +/- .024 (SE) and a y-intercept of -238.3 +/- 10.7 (SE). The maintenance energy requirement was 292 kilojoule (kJ) per kg per day (367 kJ per kg.75 per day). The regression of body RE, defined as RE minus egg energy, on MEI was linear (R2 = .96; P less than .01) with a slope of .799 +/- .045 (SE) and a y-intercept of -344.9 +/- 19.7 (SE). Therefore, an MEI of 432 kJ per kg per day was required by BB hens to maintain body energy equilibrium when they were laying at approximately 85% production. At an MEI of less than 432 kJ per kg per day, body energy was used for egg production. The AME cost of depositing 1 kJ of body, egg, protein, or fat energy was (mean +/- SE) 1.21 +/- .06, 91 +/- .32, 1.96 +/- .71, and 1.05 +/- .15 kJ, respectively. The results indicate that individually caged BB hens between 28 and 36 wk of age in a thermal-neutral environment (21 C) require approximately 1.6 megajoule (MJ) of AME per bird per day for normal growth (3 g/per day) and egg production (85%).
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