In Experiment 1, 10 microCi 45Ca/day were administered to 125 hens for 10 days. Hens were then allocated to five treatments with calcium levels ranging from .08 to 3.75% of the diet. In Experiment 2, hens with morning oviposition times were randomly allocated to 11 treatments that were periods of time postoviposition ranging from 6 hr to 24 hr, in 2-hr increments (Experiment 2). At the end of each 2-hr period, eggs from 25 hens were removed from the uterus. The 18-, 20-, and 22-hr treatments were replicated three times. In Experiment 3, hens were fed either ad libitum or feed was withheld the last 5 or 6 hr before oviposition. In Experiment 4, hens were fed 10 microCi of 45Ca for 15 days to label skeletal calcium. Hens were divided into two groups and fed a .08 or 3.75% calcium diet for 2 days. On the second day, 25 hens fed the 3.75% calcium diet were intubated with 7 g of the same diet containing .5 g calcium at 1700, 2100, 0100, 0500, and 0700 hr. The measurements used were egg weight, shell weight, and 45Ca content of the egg shell. Results indicated a significant linear or quadratic regression of dietary calcium levels on 45Ca accumulation in eggshells and eggshell weight (Experiment 1). As the calcium level of the diet increased, eggshell weight increased and 45Ca recovery decreased. Utilization of skeletal calcium for shell formation ranged from 28 to 96%. In Experiment 2, the rate of shell calcification was not constant throughout the calcification process but varied significantly.(ABSTRACT TRUNCATED AT 250 WORDS)

Dry matter and calcium content of the digestive tract were determined on two groups of broiler breeders during a 24-hr period. The individually caged hens were fed either ad lib or restricted to 122 g of feed during a 4-hr feeding period each day from 0700 to 1100 hr. The hens received artificial light from 0700 to 2300 hr. On Day 14 of the feeding program a total of 100 hens, 10 from each group, were necropsied at selected intervals (0700, 1100, 1900, 2300, 0300 hr), and the contents of the various segments of the digestive tract and feces were collected and analyzed for dry matter and calcium. The calcium analysis also included any endogenous excretions and, therefore, absorption values are apparent. Hens restricted to 122 g feed per day had only 51.7% of the dry matter and 64.2% of the calcium consumed during the 4-hr feeding period remaining in the digestive tract at 1100 hr. By 2300 hr only 20.6% of the feed and 28.1% of the calcium remained. Hens had only approximately 14% (14.2 g) of their total dry matter intake and 16% (.70 g) of the calcium available for absorption from 0300 hr. The ad lib group, with an average intake of 171 g feed per day, had consumed only 26% of their daily feed intake by 1100 hr. Fifty-five percent of the dry matter consumed and 22% of the calcium remained in the digestive tract at 1100 hr. It was concluded that broiler hens restricted to morning feeding do not maintain a constant and equal metering of dry matter or calcium from the crop into the digestive tract throughout a 24-hr period.

In Experiment 1, Hyline W36 caged hens were fed diets containing 1.7, 2.9, 3.5, and 4.1% calcium for 10 and 16 weeks. In Experiments 2 and 4, Dekalb XL and Hyline W36 pullets were fed diets containing 1.0, 1.7, and 3.75% calcium for 3 weeks (Exp. 2) or until 25 pullets from each group laid 7 eggs (Exp. 4). In Experiment 3 and 5, Dekalb and Hyline hens were fed diets containing 1.5 (Dekalb only), 1.75, 2.25, 2.75, and 3.75% calcium for 8 weeks. Criteria were liver, fat pad, egg and shell weights, egg specific gravity, production, feed consumption, liver fat and fatty acid composition, liver hemorrhage score, and body weight. As percent dietary calcium decreased, Hyline birds (Exp. 1, 4, and 5) had increased liver fat, body weight (except Exp. 4), and feed consumption, but egg specific gravity and shell weight decreased. Reduced dietary calcium levels had no effect on egg production in Experiment 1 but significantly reduced production in Experiment 5. Liver hemorrhage score significantly increased as percent dietary calcium decreased (Exp. 1). As dietary calcium decreased, Dekalb pullets (Exp. 2) had increased feed consumption, fat pad weight, and liver hemorrhage score. There was no increase in liver fat. However, in Dekalb hens (Exp. 3), feed consumption and egg production were significantly decreased as dietary calcium decreased. It is concluded that overconsumption caused by feeding pullets or hens inadequate calcium had no beneficial effect on egg size or egg production and, depending on strain, increased liver fat, liver hemorrhage score, body weight, and fat pad weight.

Experiments were conducted to determine the influence of time of dietary calcium intake on eggshell quality in broiler breeder hens. In Experiment 1, 60 hens were randomly divided among three treatment groups. The control group received 155 g feed (3.1% calcium) per day at 0800 hr whereas the morning- (a.m.) and evening-fed (p.m.) treatments received a .42% calcium diet (155 g/bird) and were intubated with 4.2 g calcium at 0800 or 1600 hr, respectively. Egg weight, shell weight, and specific gravity were determined at 3-day intervals for 15 days. In Experiment 2, 150 breeder hens were randomly divided among two treatment groups. They were fed 122 g per hen during a 2.5-hr feeding time at 0700 to 0930 or 1530 to 1800 hr. Eggs were collected for egg weight, shell weight, and specific gravity determinations. At the end of the 5th week, 10 hens from each treatment group were sacrificed at various times throughout a 24-hr period and the contents of each segment of the GI tract and feces were analyzed for moisture, dry matter, and calcium. In Experiment 3, two commercial broiler-breeder houses with 5,000 hens each were used. They were fed 132 g/hen per day at 0530 hr daily with water provided ad lib. The feeding time of one house was moved forward by 2 or 2.5 hr per day until the feeding time was 1600 hr. Eggs were collected for 2 weeks following pretreatment data and values determined for specific gravity. Eggs were also candled at 7 days incubation to determine embryonic mortality and fertility. Hens intubated at 0800 hr with their daily supply of calcium did not maintain shell quality equivalent to controls (Experiment 1). However, hens intubated at 1600 hr had no difficulty maintaining shell quality. Hens fed at 1530 hr had significantly better shell quality during all weeks tested compared to hens fed at 0700 hr (Experiment 2). The p.m.-fed hens had 66.9% more calcium available at 1800 hr (2.07 vs. 1.24 g) compared to a.m.-fed hens. Hens fed at 1600 hr in the commercial houses (Experiment 3) had significantly better eggshell quality (specific gravity) than hens fed at 0530 hr. There was no significant difference in percent embryonic mortality or percent fertility when eggs were candled after 7 days of incubation. It was concluded that p.m.-fed hens had significantly more calcium available during the stages of eggshell calcification. The result was significantly better eggshell quality.

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