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The hypothesis was proposed that the improved embryonic livability observed when higher incubation temperatures were imposed on eggs stored for 15 d prior to setting might have basis in energy metabolism. To test the hypothesis, fertilized turkey eggs were incubated either for the first 2 wk of development (experiment 1) or only the first week of development (experiment 2) at 37.8 degrees C compared with controls incubated at 37.5 degrees C. In both experiments, eggs were stored for either 15 or 3 d prior to setting. Viable embryos were selected randomly from each storage-by-incubation period treatment combination at 25 to 28 d of incubation and were sampled for blood, heart, and skeletal muscle tissues. Tissues were weighed and assayed subsequently for glucose or glycogen content. In experiment 2, the randomly selected embryos from each treatment combination were sampled at 7, 14, 21, and 28 d of incubation. Embryos at 7 and 14 d were assayed on a whole body basis, whereas at 21 and 28 d the bodies were dissected, and heart, liver, and skeletal muscle tissues were weighed and assayed for glycogen and lactate. Blood samples were collected between 25 and 28 d of incubation as in experiment 1 and assayed for glucose, creatine kinase, lactate dehydrogenase, and thyroid hormone concentrations. In both experiments, accelerated development was noted due to higher temperature and enhanced embryonic carbohydrate metabolism, and elevated thyroid hormone concentrations were observed compared with controls. It was concluded that a possible mechanism for the improved livability of faster growing embryos observed after prolonged egg storage might be due to better utilization of carbohydrate.

An experiment was designed to examine a mechanism to improve embryonic survival following maternal thyroid hormone manipulation. Commercial turkey breeder hens were fed diets containing supplemental iodide to mimic changes in the maternal thyroid output during an egg production cycle (32 to 48 wk of age). Dietary iodide treatment depressed maternal blood thyroxine (T4) concentrations in a time-dependent manner. Dietary iodide depressed maternal blood 3, 5, 3’-triiodothyronine (T3) levels across all times examined. The maternal dietary treatment increased embryonic blood concentrations of T4 at 25 to 28 d of incubation but depressed blood concentrations of T3 only at 27 d of incubation. In a second trial, the same response was noted in maternal blood when the hens were fed additional iodide with no corresponding effects on T3 concentrations. The iodide treatment decreased embryonic T4 concentrations in the second trial as well but in a time-dependent manner. Iodide accelerated the increase in T4 concentrations coincidental with earlier pipping in eggs from iodide-fed dams compared with controls. The data indicate that the embryonic thyroid function during hatching is dependent upon the maternal thyroid in turkey dams, even though the embryo develops outside the maternal body.

Functional eggshell qualities, thyroid hormones, and carbohydrate metabolism of chick embryos at the end of incubation were compared between a modern (Arbor Acres line) and a randombred control population (Athens-Canadian Randombred). Embryos from the Arbor Acres genetic line developed in larger eggs with more albumen and less yolk than Athens Canadian Randombred lines. Percentage shell and functional eggshell properties measured as eggshell conductance constants did not differ between genetic lines. On a relative basis, hearts were generally smaller and livers heavier in Arbor Acres than in Athens-Canadian Randombred birds. Heart and liver glycogen concentrations were greater in Athens-Canadian Randombred than in Arbor Acres embryos. However, blood glucose was greater in Randombred than in Arbor Acres embryos only at internal pipping, a time of hypoxia and hypercapnia. Blood plasma concentrations of thyroxine did not differ significantly between the modern and Randombred embryos at any stage examined. Modern broiler chick embryos possessed greater concentrations of triiodothyronine as well as greater triiodothyronine to thyroxine ratios than Randombred embryos at external pipping and hatching. It can be inferred from the data that chick embryos differ in their use of carbohydrate during late development between modern and Randombred genetic lines.

DeKalb XL chicks were given a beak trim at 6 d of age (6DP) with a 2.8-mm gauge and a beak trim at 11 wk (11WB) with a block cut approximately 2 mm anterior to the nasal openings. Corticosterone (CS) levels of the 6DP treatment were (P < or = 0.01) elevated above nontrimmed CS levels at 2 h posttrim; and BW and feed consumption (FC) of the 6DP were depressed until 8 wk of age. At 11 wk of age, CS of the 11WB treatment was (P < or = 0.02) elevated above controls at 1, 2, 8, and 5 wk posttrim. The 11WB treatment resulted in a decrease in FC and a reduction in BW at 12, 14, and 16 wk of age, whereas there were no differences among treatments in livability during the pullet phase. At 72 wk of age, FC of the nontrimmed controls was greater than both beak trimmed treatments, and both beak trimmed treatments had greater hen housed eggs, percentage hen day egg production, and percentage livability. Both beak trimmed treatments resulted in better egg income, feed cost per hen, and net income (NI). The 6DP and 11WB beak trim treatments resulted in an improvement of NI per hen of 1.48 dollars and 1.86 dollars, respectively. In addition, both beak trimmed treatments exhibited better feather score and Hansen's test (fearfulness). It was concluded that pullets and hens could adapt to the physiological stress of beak trimming and out perform, during a lay phase, controls whose beaks were not trimmed.

High mortality occurred in two flocks of ducklings: 20% and 50% by 4 and 7 days of age, respectively. The feeds were found to contain 300 to 1176 ppb of deoxynivalenol (DON), 4.5 ppm of fumonisin, and 10 ppb of aflatoxin B1. No other mycotoxins were detected. Pathological analysis indicated that the ducklings were dehydrated with no feed in the gastrointestinal tract. Histopathology revealed no significant lesions. A necropsy diagnosis indicated a condition similar to starve-outs and feed refusal. An infectious cause of mortality was not suspected.

Two commercial strains of 18-wk-old Single Comb White Leghorn (SCWL) hens, HyLine W-36 and DeKalb XL, were housed six hens per cage in layer cages at two densities (361 and 482 cm2 per bird) with two replications each per strain and density combination. The high density treatment contained 24 hens per replication, and the low density treatment contained 18 hens per replication. Egg production was measured during the first egg production cycle, a molt (fast) period, and the first 4 wk of the second lay cycle (20 to 68 wk of age). Blood samples were obtained from six hens from each replicate in each strain and density combination (total of 48) at 20, 26, 34, 43, 51, 62, 64, and 68 wk of age. In addition, blood samples were obtained in a random order from hens in each cage, and the sequence of sampling was recorded (1 to 6). Blood smears were made, from which heterophil to lymphocyte ratios (H:L) were determined. Radioimmunoassays were conducted to determine levels of plasma corticosterone (CS), 3,5,3'-triiodothyronine (T3), and thyroxine (T4). The results indicated that strain did not affect percentage hen-day egg production (%HDP). Strain and cage density did not affect H:L, T3, T4, or CS. However, these parameters were affected by bird age, which was related to the egg production cycle. Plasma CS significantly (P < or = 0.001) increased during peak %HDP at 26 wk and 64 wk during the molt (fast), and H:L significantly (P < or = 0.001) increased during the molt (fast) at 64 wk. The sequence in which blood samples were obtained, from hens within a cage in sampling order, also increased plasma CS. The CS was significantly (P < or = 0.001) elevated in the third, fifth, and sixth hens from which blood samples were drawn. Plasma T3 and T4 changed during the production cycle. The T3 was significantly (P < or = 0.0001) depressed during peak egg production at 26 wk and during the molt (fast) at 64 wk when compared with the other time periods. Plasma T4 was depressed (P < or = 0.0001) at 51 wk and was elevated (P < or = 0.0001) at 64 wk during the molt (fast). The physiological and metabolic parameters of the different hen strains and cage densities were similar during egg production. However, CS, T3, T4, and H:L changed with age in relation to the egg production cycle. In addition, the physiological demands of peak egg production and molt (fast) appeared to be similar.

Eggshell conductance was measured and eggshell conductance constants were calculated for eggs from ostriches. In addition, egg water, yolk, albumen, shell, and total solids were measured in an effort to determine the maternal investment of ostrich eggs. The results of the study suggest that the optimal incubator humidity for ostrich eggs is less than 25% to allow a 15% loss of initial egg mass during the 45-d incubation period. This low humidity does not preclude increasing humidity during the actual hatching process. In addition, incubation temperatures need to be adjusted to allow a longer development time for the embryo to attain an adequate level of maturity to survive the plateau stage in oxygen consumption or to prevent the use of limited energy of the yolk to survive the anoxia of tucking and internal pipping. The optimal incubation temperature of ostrich eggs appears to be between 36.1 and 36.9 C.

A study was undertaken to assess the role of sex and age on the adrenal cortical response of turkey poults during the time period associated with idiopathic poult mortality. Three and 14-day-old tom and hen turkey poults were subjected to the following treatments: saline injection (control), cool water immersion (20 C) for 1 min, cold water immersion (5 C) for 1 min, and 1 IU/kg adrenocorticotrophic hormone (ACTH) injection. Blood was collected 1 and 4 h posttreatment for plasma corticosterone (CS) assay. Temperature treatments did not affect plasma CS in either age or sex. Plasma CS was increased by ACTH after 4 h postinjection in both sexes and at both ages. The hypothalamic-pituitary-adrenal cortical axis of the turkey poult was functional but appeared to be insensitive to temperature stress.

A new flux-transfer technique has been used to measure the total neutron flux to an accuracy of 5% at the Army Pulse Radiation Facility (APRF) fast pulse reactor. Use is made of 239Pu-loaded fission chambers developed by the National Bureau of Standards (NBS) and calibrated against a 252Cf source at NBS. Advantages of the method are that it uses a standard source for calibration, that it is independent of errors in fission foil masses and that the effects of cross-section errors are minimized by the need to use only cross-section ratios. Therefore, the method can serve as a calibration procedure that is readily amenable to interlaboratory comparison. The results show that previous dosimetry is 18% too high in the APRF in-core irradiation facilities, and 21% too high at core surface. Flux calibrations have also been made by using 237Np, several uranium isotopes, and the 32S(n,p)32P reaction. Fluxes from all measurements agree to 7%. The (>10 keV/>3 Mev) flux ratios determined for the glory holes and leakage spectra are 8.4 ± 0.6 and 7.3 ± 0.5, respectively.

The study examined the relationship between plasma corticosterone (CS) levels and early mortality in Large White tom turkey poults. Trial 1 was conducted to compare the plasma CS levels of 3-day-old poults that subsequently lived or died during the first 2 wk posthatch. Blood samples were obtained from 100 poults at 3 days of age. By 2 wk of age 9% mortality had occurred. Plasma CS of poults that lived (7.1 ng/mL) was significantly greater (P less than .05) than in poults that died (3.2 ng/mL) between 3 and 14 days of age. A second trial was conducted to test the effects of feed-induced elevation of plasma CS on poult performance under stressful conditions. This trial consisted of three treatment groups: 1) control (C), poults placed immediately after removal from the hatcher with feed and water; 2) control-held (CH), poults held without feed and water at 28.9 C for 3 days posthatch; and 3) 40 mg CS/kg feed-held (40H), poults held without feed and water at 28.9 C for 3 days posthatch then fed 40 mg CS/kg feed. Mortality was monitored daily and body weights, feed consumption, and plasma CS levels were measured at 1 and 2 wk of age. The only performance parameter that was significantly affected was body weight; a significant reduction occurred at 2 wk of age in poults given the 40H treatment. It was concluded that poult death is associated with low plasma CS levels, but diet-induced increases in plasma CS did not significantly improve livability following a stressful condition.

Two trials were conducted with turkey poults to examine the ontogeny of daily rhythmicity of plasma corticosterone (CS), and to determine the plasma CS response to adrenocorticotropic hormone (ACTH) injections and temperature stress at different times during a light-dark cycle. In Trial 1, CS levels were determined at 3-h intervals over a 24-h period in 3, 10, and 14-day-old tom and hen poults maintained on a 12 h light:12 h dark (12L:12D) light-dark cycle. Plasma CS levels of tom and hen poults were similar. A robust daily rhythm in plasma CS occurred by 10 days of age, with maximal levels of CS occurring during the scotophase. In Trial 2, daily variation in plasma CS sensitivity to cold treatment or ACTH in 2-wk-old toms was examined. Tom poults were exposed to cold water immersion (5 C for 1 min), porcine ACTH injection (1 IU/kg), or saline injection at 1100 h in midphotophase and at 2300 h in midscotophase. Treatments significantly increased plasma CS in both the photophase and scotophase, with the levels being significantly higher in the scotophase. At midphotophase cold or ACTH treatment induced, respectively, a 489 and 546% increase in plasma CS above that of controls. During midscotophase, 746 and 695% increases in CS above levels for controls were induced by cold stress or ACTH, respectively. Differences between percent changes for times of day were not significantly different. It was concluded that a daily rhythm in plasma CS in turkey poults grown under a 12L:12D light-dark cycle occurs between 3 and 10 days of age, with maximum levels occurring during the scotophase. A daily variation in the adrenal cortical response to exogenous ACTH or cold water treatment in excess of the normal plasma CS rhythm was not apparent.

Day-old tom poults were exposed to one of the following light treatments: 1) continuous incandescent light (24LL), 2) 23L:1D incandescent light, 3) 12L:12D incandescent light, or 4) natural day lengths only. Mortality was recorded daily. At Weeks 1, 2, 4, 6, and 8, after poult placement, body weights and feed consumption were measured. At each of these times, 10 poults were sacrificed from each treatment group for evaluation of plasma corticosterone. Day lengths utilized in this study had no consistent effect on poult-performance parameters except from 0 to 2 weeks of age. During this time, poults in the 24LL and 23L:1D treatments consumed less feed but were similar in body weight to poults in the other treatments. Adrenal function was also not consistently affected by day length. However, in all treatment groups plasm a corticosterone was lowest during the first 2 weeks posthatching, when compared to hormone levels at 4, 6, and 8 weeks. The lower corticosterone that occurred during the first 2 weeks posthatching may be involved in early poult mortality.

The current study investigated whole-body O2 consumption, intestinal O2 consumption, and intestinal inflammation status through mucosal cytokine production on broiler chicks fed the direct-fed microbial PrimaLac. One hundred twenty 1-d-old broiler chicks were randomly assigned to 1 of 3 experimental diets: standard starter diet (control), standard starter diet with added salinomycin (SAL), and standard starter diet with added PrimaLac (DFM). Birds were housed in 2 separate rooms, the control and SAL treatments in one room and the DFM in another. Intact ileal and cecal samples were collected on d 19, 20, and 21 after measuring whole-body O2 consumption using indirect calorimetry. The O2 up-take of ileal tissue was measured using an in vitro O2 monitor. Analysis of intestinal immune status of broilers was measured by the relative differences in mRNA of both pro- and antiinflammatory cytokines: interleukin-(IL) 1beta, IL-6, and IL-10 using real-time reverse transcription-PCR. Broilers exhibited a 6 to 16% decrease in whole-body energy expenditures and up to a 47% decrease (P0.05) in ileal energy expenditures in the DFM group compared with other treatments. The reverse transcription-PCR data demonstrated that DFM consortium numerically altered both pro- and antiinflammatory cytokines within the ileum of 19-d posthatch broilers. These data suggest that direct-fed microbials like PrimaLac increase metabolic efficiency via changes in intestinal physiology and metabolism.