Molting is a common practice used by the commercial egg industry to rejuvenate flocks for a second or third laying cycle. During this time the hens rest from production, and the reproductive organs are rejuvenated to increase production and quality during the next laying cycle. Although feed withdrawal (FW) is the most popular and effective method of molt induction, it has come under scrutiny due to food safety issues and animal welfare issues. This study involved feeding alfalfa mixed with layer ration at different ratios to hens to determine their ability to induce molt. The treatment ratios were 100% alfalfa (A100), 90% alfalfa and 10% layer ration (A90), and 70% alfalfa and 30% layer ration (A70). In addition, a fully fed (FF) nonmolted control and a FW negative control were used. Alfalfa is an insoluble, high fiber feedstuff with low metabolizable energy. Egg production for A90 and FW treatments ceased completely by d 6, whereas birds fed A100 and A70 ceased egg production by d 8. Ovary and oviduct weight of hens fed all molting diets decreased (P < 0.05) by an average of 1.5 to 2.5% (BW basis) compared with FF control during the 9-d molt induction period. As the percentage of layer ration increased, feed intake also increased and percentage of BW loss decreased during the 9-d molt induction period. Hens molted by FW lost an average of 25.8% BW, whereas A70 hens lost 18.9% BW. Nonmolted hens (FF) and A70 treatment hens had significantly lower (P < 0.05) egg production when compared with all other treatments over the 39-wk postmolt period. FF treatment hens also had lower (P < 0.05) albumen heights when compared with all other treatments. From these results, alfalfa or alfalfa mixed with layer ration appears to be viable alternatives to conventional FW methods for the successful induction of molt and retention of postmolt performance.

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The standard method for molting to stimulate multiple egg-laying cycles in laying hens is feed deprivation. However, the physiological changes within hens caused by feed deprivation increase susceptibility of the hens to Salmonella enterica serovar Enteritidis (SE) infection. In an effort to develop an alternative method to induce molting without increasing susceptibility to SE, an alfalfa diet was compared with the standard molting method for the level of ovary regression and SE colonization. Hens over 50 wk of age were divided into 3 treatment groups (12 hens/group): nonmolting by normal feeding (NM), molting by feed deprivation (M), and molting by alfalfa diet (A). Individual hens on all treatments were challenged orally with 10(5) cfu of SE on the fourth day after feed changes and were analyzed for ovary weight and SE colonization or invasion in crop contents, cecal contents, liver, spleen, and ovary on the ninth day. In 3 of the 4 trials, there was a significant decrease in SE colonization of the crop between the alfalfa diet (A) and the feed deprived molt (M). In most of the 4 trials, there was a significant reduction in SE infected organs in birds fed the alfalfa diet (A) compared with birds undergoing feed deprived molt (M). Most of the trials showed no significant difference in overall SE between A and NM. Therefore, the results of this study suggest that an alfalfa diet has the potential to be used as an alternative method for forced molting, without increasing the incidence of SE in eggs and internal organs.

Aims:  To detect the presence of methanogens in the faeces of broiler chicks during the first 2 weeks of age. Methods and Results:  Chicken faecal samples from 120 broiler chicks were incubated for methane gas formation and methanogenic archaea were analysed using real‐time PCR. The copy number of the order Methanobacteriales 16S rDNA gene in chicken faeces when the broilers were 3–12 days of age, litter and house flies collected in the bird house ranged from 4·19 to 5·51 log10 g−1 wet weight. The number of positive methane culture tubes increased from 25% to 100% as the birds aged. Conclusions:  Methanogens were successfully detected in faecal samples from 3‐ to 12‐day‐old broilers, as well as litter and house flies using real‐time PCR. The copy number of methanogenic 16S rDNA gene in these samples was also similar to the number observed in litter and house flies. Significance and Impact of the Study:  The same methanogens consistently appeared in chicken faeces a few days after birth. Detection of the methanogenic bacteria in litter and house flies implicated them as potential environmental sources for methanogen colonization in broiler chicks.

A study was conducted to evaluate effects of different bone preparation methods on bone parameters and the correlations between bone breaking strength and the other bone parameters. Bone breaking strength is dramatically changed depending on bone preparation methods, whereas other bone parameters such as ash content and ash concentration are not significantly influenced by bone preparation methods. Thus, the objective of this study was to evaluate the effects of 3 bone preparations (fresh, dry, and fat-free dry) on bone parameters and the relationship between bone breaking strength and bone parameters. Sixty Single Comb White Leghorn hens were used for this study. Hens were euthanized by CO2 gas, and the right tibia and femur were collected. The bones were divided into 3 treatment groups: fresh, dry, and fat-free dry. There were no significant differences in fresh weight, bone volume, dried weight, ash weight, and ash concentration of tibia and femur among the treatments. However, fresh tibia (24.13 kg) exhibited more bone breaking strength compared with the dried (9.90 kg) and fat-free dried bones (7.41 kg) (P < 0.05). The bone breaking strength (20.97 kg) of fresh femur was also significantly higher than the dried (9.22 kg) and fat-free dried femurs (6.94 kg). The bone breaking strength of the fresh bone was highly correlated with dried weight, ash weight, and ash concentration, whereas that of the fat-free dried bone was poorly correlated with the other bone parameters. The results indicate that fresh bone gives better bone breaking strength correlated to the other bone parameters than dry or fat-free dry preparation.