Groups of 18 hens, 230 days of age, were housed in each of three climatic chambers with light schedules of 14L:10D. One was maintained at a constant temperature of 23.9 C, the second was cycled between 15.6 and 37.7 C (mean, 26.7 C), and the third was cycled between 21.1 and 37.7 C (mean, 29.4 C). In Experiment 1, the high temperature peaked during the dark period at 0200 hr and in Experiment 2, the high temperature peak was at 1400 hr during the light period. The birds had free access to a commercial breeder feed in these two experiments. The results from three 2-week observation periods indicated no significant differences in percent hen-day production, grams of feed per gram of egg mass, or overall body weight change but feed intake per day, egg weight, and shell thickness were significantly reduced by mean temperatures of 26.7 and 29.4 C in cycling chambers. The pair-feeding of birds in the 23.9 C constant chamber compared with those in the cycling 29.4 C chamber resulted in production of significantly heavier eggs with thicker shells without significantly influencing any of the other parameters. The reductions in egg weight and shell thickness observed at cyclic temperatures were not simply a result of a reduction in nutrient intake at high temperatures but also the direct effect of heat stress on the hens. In the 23.9 C constant temperature chambers, a reduction in AME of the feed for the hens fed ad libitum was observed but not for hens pair-fed to hens in the 29.4 C cyclic chamber.
Grains produced by low-phytate barley and corn isolines homozygous for each species' respective low phytic acid 1-1 allele were compared to grain produced by near-isogenic normal or wild-type barley and corn in broiler chick feeds. Cobb x Cobb (384) chicks were used in a 10-d study. A randomized complete block design with a factorial arrangement of 2 x 2 x 3 was used with 4 replicates (8 chicks / replicate) per treatment. Twelve isocaloric and isonitrogenous treatment diets were formulated to contain 2 types of grain (barley and corn), 2 levels of grain (40% and 60%), and 3 sources of available P (wild-type grain, wild-type P-supplemented grain, and low-phytate grain). Growth parameters, bone parameters, total bone mineral, and apparent digestibilities were measured. The mean growth and bone responses were 1) higher for barley diets compared to corn diets, 2) higher for 60% grain inclusion compared to 40%, 3) higher for low-phytate compared to wild-type grains, and 4) not different for low-phytate compared to P-supplemented wild-type grain diets. Chicks fed low-phytate-based diets excreted 33 and 43% less P than chicks fed wild-type and P-supplemented wild-type diets, respectively. Correlations between percentage bone ash, total bone ash, and bone strength indicated a strong relationship and appear to support the use of bone strength analysis as a simpler method than ash content determination as an indication of P status. Feeding low-phytate grains will reduce the need for supplemental P in chick diets.
Candling hatching eggs during incubation and breakout examination of the clear eggs or dead embryos are useful tools for hatchery managers to use in maintaining quality assurance and analyzing poor hatches. Other tools include monitoring the temperature of the egg storage room, incubator temperature, incubator humidity, shell quality, chick quality, hatching percentage, bacterial counts in air or on hatchery surfaces, and egg moisture loss during incubation. This publication illustrates various conditions that may be seen in eggs during candling and describes how to identify infertile eggs and early dead embryos during breakout. It is best used in conjunction with Common Incubation Problems: Causes and Remedies (ANR Publication 8127) and the video Hatching Egg Breakout (ANR Video V86-W) (see "For More Information" at the end of this publication). This publication also contains a glossary of technical terms.
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