Production performance and egg quality were compared between 4 strains of beak-trimmed layers: 3 commercial strains-Lohmann White (LW), H&N White (HN), Lohmann Brown (LB)-and a noncommercial cross between Rhode Island Red (male) and Barred Plymouth Rock (female) in conventional cages and in floor pens. All chicks were reared and 857 pullets were housed at 18 wk of age in their respective environments. Body weight, hen-day egg production, feed consumption and efficiency, and egg quality were measured at wk 20, 30, 40, and 50. In floor pens, the location of eggs was recorded for 4 consecutive days at 4-wk intervals between 20 and 50 wk of age. Eggs from cages, nest-boxes, and the floor were tested for Escherichia coli and coliform contamination at 38 and 42 wk of age. Mortality was recorded during the rearing and laying periods. Housing systems significantly influenced BW and mortality but not feed consumption or feed efficiency. The interaction between environment and strain was significant for hen-day egg production at wk 20 to 30 and for BW at wk 30, 40, and 50. Hens in floor pens had greater BW, egg and yolk weights, and yolk color than those in cages. Commercial hens produced more eggs than the cross hens. Overall, HN hens had the best production performance, whereas cross hens had better egg quality. In floor pens, LW and HN hens laid most of their eggs in nest boxes, whereas LB and cross hens laid half of their eggs on the floor. Eggs from cages had lower E. coli and coliform contamination than those from nest-boxes and the floor, and E. coli contamination was greater for LB eggs than for LW eggs. Significant strain differences were found for the use of nest-boxes, with a high percentage of floor eggs for brown egg strains. This study suggests that genotype x environment interactions should be considered when alternative housing systems are proposed.

No abstract

During the 1992 breeding season, eggs of bald eagles (Haliaeetus leucocephalus) were collected within a gradient of exposure to chlorinated hydrocarbon pollutants, particularly from pulp mill point sources, on the southern coast of British Columbia, Canada. Twenty-five eggs were placed in a laboratory incubator, of which 18 hatched; chicks were sacrificed within 24 h. Hatching success was not significantly different between eggs taken from pulp mill sites and reference sites. A hepatic cytochrome P4501A (CYP1A) cross-reactive protein was induced nearly sixfold in chicks from near a pulp mill at Powell River compared to those from a reference site (p Ͻ 0.05). Hepatic ethoxyresorufin-O-deethylase (EROD) and benzyloxyresorufin O-dealkylase (BROD) activities were also significantly elevated in chicks from nests located near pulp mills compared to reference sites (p Ͻ 0.0005 and p Ͻ 0.02, respectively). A hepatic CYP2B cross-reactive protein was threefold higher in chicks from pulp mill versus reference sites, but the difference was not significant. Residual yolk sacs of eggs collected near pulp mill sites contained greater concentrations of 2,3,7,8substituted polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) compared to reference areas. No significant differences in concentrations of polychlorinated biphenyls (PCBs), non-ortho congeners, and organochlorine pesticides occurred among sites. Regressions showed that the hepatic CYP1A cross-reactive protein and EROD and BROD activities were positively correlated with 2,3,7,8-TCDD, 2,3,7,8-TCDF, and toxic equivalents (TEQs WHO -World Health Organization toxic equivalence factors) in yolk sacs. No significant concentration-related effects were found for morphological, physiological, or histological parameters, such as chick growth, edema, or density of thymic lymphocytes. Using hepatic CYP1A induction as a biomarker, a no-observedeffect-level (NOEL) of 100 ng/kg and a lowest-observed-effect-level (LOEL) of 210 ng/kg TEQs WHO on a whole egg (wet weight basis) are suggested for bald eagle chicks. Keywords-Bald eagleEmbryotoxicity TCDD Non-ortho PCBs P450Chlorinated hydrocarbon effects on bald eagles Environ. Toxicol. Chem. 15, 1996 783 Environ. Toxicol. Chem. 15, 1996 J.E. Elliott et al. Environ. Toxicol. Chem. 15, 1996 J.E. Elliott et al.Council of Canada. This project was part of a Ph.D. project on toxicology of chlorinated hydrocarbons in British Columbia bald eagles.

No abstract

There have been few studies on quantifying carotenoid accumulation in carrots, and none have taken the comparative approach. The abundance and distribution of carotenes in carrot roots of three varieties, white, orange, and high carotene mass (HCM) were compared using light and transmission electron microscopy (TEM). Light microscopy has indicated that, in all three varieties, carotenes were most abundant in the secondary phloem and this area was selected for further TEM analysis. While carotenes were extracted during the fixation process for TEM, the high-pressure freezing technique we employed preserved the spaces (CS) left behind by the extracted carotene crystals. Chromoplasts from the HCM variety contained significantly (P < 0.05) more CS than chromoplasts from the orange variety. Chromoplasts from the white variety had few or no CS. There was no significant difference between the HCM and orange varieties in the number of chromoplasts per unit area, but the white variety had significantly (P < 0.05) fewer chromoplasts than the other two varieties. A large number of starch-filled amyloplasts was observed in secondary phloem of the white variety but these were not found in the other two varieties. The results from this comparative approach clearly define the subcellular localization of carotenoids in carrot roots and suggest that while the HCM genotype was selectively bred for increased carotene content, this selection did not lead to increased numbers of carotene-containing chromoplasts but rather greater accumulation of carotene per chromoplast. Furthermore, the results confirm that roots of the white carrot variety retain residual amounts of carotene.

No abstract

A great blue heron colony located near a pulp mill in British Columbia failed to fledge young in 1987, with a concurrent sharp increase in polychlorinated dibenzo-p-dioxin (PCDD) and polychlorinated dibenzofuran (PCDF) levels in their eggs. In 1988 we tested the hypothesis that the PCDD and PCDF contamination caused reproductive failure by increasing mortality of the heron embryos in ovo. Pairs of great blue heron eggs were collected from three British Columbia colonies with low, intermediate, and high levels of dioxin contamination: Nicomekl, Vancouver, and Crofton, respectively. One egg of each pair was incubated under laboratory conditions at the University of British Columbia (UBC) while the other egg was analyzed for PCDDs and PCDFs. All incubated eggs were fertile. All eggs from the Nicomekl colony hatched, while 13 of 14 eggs from Vancouver and 12 of 13 eggs from Crofton hatched. Subcutaneous edema was observed in 4 of 12 chicks from Crofton and 2 of 13 chicks from Vancouver. No edema was seen in the chicks from Nicomekl. There was a small, but significant, negative regression of plasma calcium concentration, yolk-free body weight, tibia length, wet, dry, and ash weight, beak length, and kidney and stomach weight of the hatched chicks on the tetrachlorodibenzo-p-dioxin (TCDD) level of the paired eggs. Fewer down follicles were present on the heads of TCDD-contaminated chicks. Hence while dioxins did not cause mortality of the heron embryos in ovo, the depression of growth and the presence of edema are suggestive that dioxins at the levels found in the environment have an adverse effect on the development of great blue heron embryos.

Previous observations of forced copulation (FC) in captive Mallards (Anas platyrhynchos) showed that most FC attempts were directed at females in prelaying and laying condition and that most FC's occurred in the morning when the females were leaving their nests after egg laying. In order to determine whether or not there is a physiological basis for these observed temporal patterns, sperm competition in captive Mallards was examined using artificial insemination and genetic markers. Results indicated that if a female was inseminated with two competing doses of semen at different time intervals, the proportion of progeny from the first and the second inseminations was not significantly different if these inseminations were simultaneous, 1 h, or 3 h apart. There was a preponderance of progeny (70%) from the second insemination, however, if the inseminations were 6 h apart. Insemination of females less than 1 h after egg laying resulted in 25% of the eggs laid the following morning being fertile. Only 1 of 179 eggs laid the following morning was fertile when the females were inseminated more than 1 h after egg laying. Our experiment demonstrated that there is an insemination "window," a short period when new sperm are least likely to meet competition from sperm already in the oviduct and from sperm introduced later, and it provided a possible explanation for the observed timing of FC attempts.