Objective For many generations, most species of farm animals have been subjected to intense and strictly targeted selection for improvement of their performance traits. This has led to substantial changes in animal anatomy and physiology, which resulted in considerable differences between the current animal breeds and their wild ancestors. The aim of the study was to determine whether there is breed-specific variability in behaviour as well as differences in emotional reactivity and preferences of laying hens. Methods The investigations involved 50 Green-legged Partridge, 50 Polbar, and 50 Leghorn hens. All birds were kept in the same conditions, and the behavioural tests were carried out at 30 weeks of age. We used the tonic immobility test and a modified open-field test including such objects as water, commercial feed, feed enriched with cereal grains, finely cut straw, and insect larvae, a sandpit, a mirror, and a shelter imitating a hen nest. Results The research results demonstrate that the birds of the analysed breeds differ not only in the excitability and emotional reactivity but, importantly, also in the preferences for environment-enriching elements. Ensuring hens’ well-being should therefore be based on environmental modifications that will facilitate acquisition of essential elements of chickens’ behaviour. The greatest emotional reactivity was found in the Leghorn breed, which may be a result of correlated selection aimed at an increase in chicken productivity. Conclusion The differences in the behaviour of the birds from the analysed breeds indicate that laying hens cannot be regarded as one group of animals with the same environmental requirements.

The aim of the study was to associate behavioural reactions of laying hens with the level of stress and to answer the question whether it is possible to select reactions that will facilitate phenotypic assessment of the level of stress in these birds. The investigations were carried out in 50 Green-legged Partridge, 50 Polbar and 50 Leghorn birds. A modified open-field test (MOFT) and a tonic immobility test were applied. Next, the quality of feathers was evaluated and the level of corticosterone in the feathers was determined. The corticosterone level was assessed in relation to the genetic group and feather quality and in relation to the probability of the presence/absence of specific physiological-behavioural reactions. The analysis of the results revealed no correlations between the corticosterone level in the feathers and the quality of the feathers. In turn, there was a correlation between the hen breed and the corticosterone level in the feathers: a significant difference was found between Zk and Pb hens. It was demonstrated that the corticosterone level was significantly higher in birds that exhibited such behaviours as preening in the open-field test. To sum up the results, it can be concluded that such behaviours as feather preening and latency until tonic immobility occurs can be indicators of stress in laying hens. HIGHLIGHTSThere was a correlation between the breed and the corticosterone level in the feathers: there was a significant difference between the Green-legged Partridge (3.97 ± 0.17) and Polbar (4.50 ± 0.19) hens. No significant correlations were found between the corticosterone level and the behavioural reactivity in the analysed hens. It was demonstrated that the corticosterone level was significantly higher in birds that exhibited self-grooming behaviours in the open-field test (4.61) than in hens that did not show such behaviours (3.91). ARTICLE HISTORY

This study aimed to develop a methodology for using ultrasonic technology (USG) to record eggshell thickness for selection of layers. Genetic correlations between eggshell strength and its thickness have been reported to be around 0.8, making shell thickness a selection index candidate element. Applying ultrasonic devices to measure shell thickness leaves an egg intact for further handling. In this study, eggs from 2 purebred populations of Rhode Island White (RIW) and Rhode Island Red (RIR) hens were collected on a single day in the 33rd week of the farm laying calendar from 2,414 RIR and 4,525 RIW hens. Beginning from the large end of the egg, measurements were taken at 5 latitudes: 0º (USG0), 45º (USG45), 90º (USG90), 135º (USG135), and 180º (USG180). To estimate the repeatability of readings, measurements were repeated at each parallel on 3 meridians. Electronic micrometer measurement ( EMM: ) were taken with an electronic micrometer predominantly at the wider end of eggs from 2,397 RIR and 4,447 RIW hens. A multiple-trait statistical model fit the fixed effect of year-of-hatch × hatch-within-year, and random effects due to repeated measurements (except EMM) and an animal's additive genetic component. The shell was thinnest in the region where chicks break it upon hatching (USG0, USG45). Heritabilities of shell thickness in different regions of the shell ranged from 0.09 to 0.19 (EMM) in RIW and from 0.12 to 0.23 (EMM) in RIR and were highest for USG45 and USG0. Because the measurement repeatabilities were all above 0.90, our recommendation for balancing egg strength against hatching ease is to take a single measurement of USG45. Due to high positive genetic correlations between shell thickness in different regions of the shell its thickness in the pointed end region will be modified accordingly, in response to selection for USG45.

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The aim of the study was to determine whether birds of different breeds, with different preferences for environmental elements and kept in identical conditions, would exhibit different behaviour and stress levels. The research material consisted of 50 laying hens of the Green-legged partridge (Zk), Polbar (Pb), and Leghorn (Lg) breeds. The birds were provided with identical environmental conditions. They were kept on litter in separate boxes, with 25 individuals of one breed per box, in the same building. An open field test was used in determining the behaviour of the birds. Levels of cortisol in serum and corticosterone in feathers were evaluated, and haematological and biochemical analyses of blood were performed. Leghorns proved to be a highly excitable and active breed whose needs cannot be fully satisfied in the standard conditions of large farms. Based on a differential leukocyte count, their hyperactivity was associated with increased stress. The Green-legged partridge exhibited the lowest stress levels. Birds kept in the same environmental conditions were found to differ significantly in the level of stress, probably because of differences in their behavioural needs and the possibilities of satisfying them. To reduce stress levels and improve the welfare of hens, it is necessary to verify their preferences first. Stress indicators are elevated in highly excitable birds, and the conditions on large farms are not conducive to meeting their behavioural needs. Keywords: behavioural test, blood indices, corticosterone, laying hens

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In Poland, the number of wild red foxes (Vulpes vulpes L.) and the size of the fur-farming industry are growing. There is concern that the gene pool of the wild foxes is being infiltrated by that of the farm animals. We analyzed three groups-Polish farm foxes and wild-living animals from Poland and North America-to investigate the gene flow or introgression between farm and wild red foxes. We took into account the breeding history of the species and the evolutionary relationships between fox populations on different continents. We compared the haplotypes based on the concatenated nucleotide sequences of MT-CO1 (mitochondrially encoded cytochrome c oxidase I) and MT-ATP6 (mitochondrially encoded ATP synthase 6) genes. It was confirmed that investigated fur-farm animals originated from wild individuals living in North America. We found a haplotype common to wild foxes from Europe (Poland) and wild North American individuals. The common haplotype shared by both investigated wild-living groups could indicate some degree of introgression between Polish farm and wild-living populations. Haplotypes characteristic of North American foxes were transferred to the Polish wild population and have been established. However, the pairwise Φ ST values make it clear that North American wild and Polish wild foxes are genetically distinct evolutionary groups.