26 research outputs found

    Personalities in female domesticated pigs: behavioural and physiological indications

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    The inconclusive evidence so far on the existence of distinct personality types in domesticated pigs, led us to perform the present experiment. A total of 128 gilts from 31 sows were systematically studied from birth to slaughter in two identical trials. Intra-test consistency in individual behavioural andror physiological reactions was studied in three different tests. We were not able to show consistencies in reactions of gilts over time to a backtest (at 2–4 days and 4 weeks of age) and to a novel environment test (at 10 and 24 weeks of age). Individual aggression, however, as measured in a group-feeding competition test in stable groups (at 10 and 24 weeks of age), proved to be highly consistent. Explanations for these discrepancies in intra-test consistencies are critically discussed. Inter-test consistencies were determined by relating the individual reactions of gilts to the backtest to various characteristics and responses to tests at a later age. The highest correlations were found when resistance in the first backtest was involved. No evidence was found for the existence of specific isolated categories of animals with respect to this resistance. For further analysis, extreme responding gilts in the first backtest (roughly the top and bottom 25% of the distribution) were classified as low resistant (LR; <3 escape attempts; n=31) or high resistant (HR; >4 escape attempts; n=45). By comparisons of mean responses of LR and HR gilts within groups, we have established a relationship between the backtest and several other variables. Behaviourally, the HR gilts showed more aggression in the group-feeding competition tests. Also, in the competition for the most productive teats at the anterior, a predominant position of HR piglets at this site was observed during the suckling period. The latter piglets also gained more weight during this period than LR ones. Compared to HR pigs, in the first novel environment test LR pigs hesitated longer to leave their home pens and to contact a human, but no difference in their locomotory behaviour was observed. Contrasts between LR and HR pigs in the second novel environment test were reduced or absent. Physiologically, when compared to HR gilts, LR ones had a higher reactivity of the hypothalamic–pituitary–adrenocortical (HPA) system. This was shown by higher cortisol responses to the first novel environment test, to routine weighing at 25 weeks of age, and to administration of a high dose of ACTH. It is discussed that these findings for LR and HR gilts, may provide support for the existence of behavioural and physiological responses in pigs, resembling those of proactive and reactive rodents.

    Effects of environmental enrichment on behavioral responses to novelty, learning, and memory, and the circadian rhythm in cortisol in growing pigs

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    Previously we showed that pigs reared in an enriched environment had higher baseline salivary cortisol concentrations during the light period than pigs reared under barren conditions. In the present experiment, it was investigated whether these higher baseline salivary cortisol concentrations were a real difference in cortisol concentration or merely represented a phase difference in circadian rhythm. The effects of different cortisol concentrations on the behavioral responses to novelty and learning and long-term memory in a maze test were also studied in enriched and barren housed pigs. At 9 weeks of age enriched and barren housed pigs did not differ in baseline salivary cortisol concentrations nor in circadian rhythm, but at 22 weeks of age barren housed pigs had a blunted circadian rhythm in salivary cortisol as compared to enriched housed pigs. The differences in baseline salivary cortisol concentrations between enriched- and barren-housed pigs are age-dependent, and become visible after 15 weeks of age. Enriched- and barren-housed piglets did not differ in time spent on exploration in the novel environment test. Barren-housed pigs had an impaired long-term memory in the maze test compared to enriched-housed pigs; however, no differences in learning abilities between enriched- and barren-housed pigs were found. Because blunted circadian cortisol rhythms are often recorded during states of chronic stress in pigs and rats or during depression in humans, it is suggested that the blunted circadian rhythm in cortisol in barren-housed pigs similarily may reflect decreased welfare.

    Implications of coping characteristics and social status for welfare and production of paired growing gilts

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    This paper considers the question whether knowledge on individual coping characteristics of growing pigs may be used to improve welfare and production after mixing. Gilts with either reactive or proactive coping characteristics were identified according to behavioural resistance in a backtest, respectively, being low (LR) and high resistant (HR) in this test. At 7 weeks of age, several pairs of unfamiliar gilts were formed, and pairs and dominance relationships were studied over a 3-week period. The following pairs (combinations) were established: two LR gilts (LR/LR; n = 12), two HR gilts (FIRM; n = 12), one LR and one HR gilt (LR gilt dominant: LR(d)/HR; n = 11), and one LR and one HR gilt (HR gilt dominant: LR/HR(d); n = 12). Results showed that on the day of mixing, aggression subsided less quickly and increases in body temperature were higher in LR/ HR(d) and HR/HR pairs. Also, during the first week post-mixing, feed efficiency was lower and skin damage was higher in LR/HR(d) and HR/HR pairs. Mixing of two HR gilts caused highest levels of stress, indicated by greater catecholamine concentrations in urine following the day of mixing, and higher baseline levels of plasma ACTH at I week post-mixing. The lower tendency of fearfulness. In contrast to gilts within HR/HR pairs to contact a novel object may present higher those of LR/HR(d) pairs, responses of LR(d)/HR pairs revealed much lower levels of stress, which emphasised the importance of dominance relationships, being independent of coping characteristics of individual gilts. We speculate that in LR/HR pairs, dominant LR gilts were able to suppress aggressiveness of HR subordinates. HR or proactive gilts, however, may become aggressive when being dominant. General effects of social status, independent of combination, were also found. Compared to dominants, subordinates showed higher acute cortisol, body temperature and vocal responses to mixing. In the longer term, they showed a higher vocal and parasympathetic responsitivity towards the novel object, and their body growth was impaired. Measures not influenced by combination and social status included those of leucocyte subsets, prolactin, and average heart rates during novelty tests. To conclude, aggressive conditions in newly formed groups. and consequently welfare and production, may largely depend on coping characteristics of individual pigs, but also on dominance relationships. Accordingly, the practical value of the backtest is being discussed. (C) 2002 Elsevier Science B.V. All rights reserved

    Behavioural and physiological consequences of acute social defeat in growing gilts: effects of the social environment

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    Endocrine, behavioural and immunologic processes, together with body growth, were evaluated in gilts that were defeated at 10 weeks of age in resident-intruder tests. Immediately after defeat, gilts were either separated from or reunited with a familiar conspecific (litter-mate; always a barrow). Gilts were assigned to one of four treatments: (a) DI: defeat, followed by isolation (separation from original litter-mate; n=8); (b) I: no defeat, isolation (control group; n=9); (c) DP; defeat, followed by pair-housing (reunion with original litter-mate; n=8); and (d) P: no defeat, pair-housing (control group; n=8). The following general conclusions were derived: (1) social defeat caused pronounced short-term elevations in hypothalamic-pituitary-adrenal (HPA) and sympathetic-adrenal medullary activities, and of prolactin levels. Moreover, as soon as 1 h after defeat, percentages of blood lymphocytes and neutrophilic granulocytes were, respectively, decreased and increased; (2) social defeat had some long-lasting influence on behaviour and physiology, but isolation predominantly determined responses in the longer term. Defeat, as well as isolation, resulted in increased cardiovascular activities compared to P controls, as observed in a novel object test (NOT: +7 days) and an aversion test (AVT: +14 days). Moreover, defeated as well as isolated gilts did not habituate to a repeated novel environment test (NET: -7, +2 and +7 days) in terms of frequencies of vocalising, whereas P controls did. Isolation, through the separation from any other pig, was responsible for the other observed long-term characteristics, which developed progressively. Isolated gilts showed high mobilities and high cortisol responses in the repeated NET (+7 days), not being habituated. This contrasted the reactions of pair-housed gilts, which were much reduced. In addition to their high cardiovascular activities in the NOT and the AVT, isolated gilts also displayed higher heart rates in the repeated NET and during human presence following the NOT, compared to pair-housed gilts. Finally, isolated gilts were more inhibited to approach a novel object (in the NOT) than pair-housed pigs; and (3) stress responses of defeated gilts were modulated by the subsequent social environment. Stimulation of the HPA-axis (plasma- and salivary cortisol) was prolonged in those defeated gilts which were isolated (observed in the first hour). Changes in leucocyte subsets were still observed after 3 days in DI, but were `normalised' within 1 day in DP gilts. Two days after defeat, habituation to the repeated NET in terms of mobility and salivary cortisol responses occurred in control and DP gilts, but not in DI gilts. We argue that these effects of the social environment shortly after defeat were related to a stress-reducing effect of a stable social relationship, i.e. social support.

    Resting behavior of broilers reared with or without artificial brooders

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    Rest and sleep are important for the welfare of mammals and birds. A large part of the daily time budget of broiler chickens is taken up by resting behavior and the quality of resting is important. However, in intensive broiler production systems, disruptions of resting behaviors are common. These disruptions of resting behavior could be negative for the health and growth of the birds. This study investigated if artificial brooders that provide a delimited and darker resting place, away from active birds, reduce disruptions of resting behavior compared to a control situation without artificial brooders. Six pens of each treatment were used in the same building, keeping 60 chickens (Ross 308) per pen. The artificial brooders were removed at 21 days of age. Data on disturbances and duration of resting bouts and activity between resting bouts were collected on 20 and 34 days of age. Also, as an indicator of the quality of rest, the animals' cognitive performance was evaluated in a spatial learning test that was performed at 11 days of age. The results showed that birds housed in pens with access to brooders have longer resting bouts (260.7 ± 5.2 vs. 132.8 ± 5.3s, p &lt; 0.001) and are less likely to be disturbed during resting by other individuals (0.15 vs. 0.48, p &lt; 0.001). The effect of the artificial brooders on both the duration of resting bouts and the proportion of disturbances remained after the removal of the brooders at 21 days of age. The duration of activity between resting bouts was shorter if the resting bout was ended by a disturbance (9.98 ± 1.0 vs. 61.0 ± 2.4s, p &lt; 0.001). Birds reared with brooders were more likely to solve the spatial learning task (0.5 vs. 0.27, p &lt; 0.01), but those succeeding were not faster at solving it. Broilers may be exposed to disrupted rest due to the lack of a dedicated resting place separated from areas with high activity. Using artificial brooders reduces disturbances but does not eliminate them. Therefore, additional changes to the housing conditions or management will be needed to prevent disturbances

    Some observations on the development of feather-pecking in poultry.

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    In: Applied Animal Behaviour Science, vol. 12, pp. 145-157Onderzoeksbibliografie Frank OdbergHerkomst: Onderzoeksbibliografie van em. prof. dr. Frank O. Ödberg, verbonden aan de Vakgroep Voeding, Genetica en Ethologie van de Faculteit Diergeneeskund

    Safeguarding farm animal welfare

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    Animal welfare is an important aspect of the acceptability and thus sustainability of animal production systems in Europe and, increasingly, in the rest of the world. In this chapter, we will first describe some developments in animal production and the related societal discussion on animal welfare with focus on the European Union. Then we will discuss animal welfare research and welfare assessment and we illustrate the case of the development of the Welfare Quality® protocols promoted by the European Union. Finally, we address current initiatives for improving the transparency of the market for animal-friendly produced products via labelling as well as technological developments for improving animal welfare

    Reduction in feather pecking and improvement of feather condition with the presentation of a string device to chickens

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    Feather pecking remains a serious problem in commercial egg production. It has been argued that feather pecking occurs as a result of misdirected pecking, so a possible solution would be to increase the likelihood that such pecking was targeted at another object in the environment rather than to the feathers of conspecifics. Chickens of various strains and ages will readily peck at a device consisting of strands of white string but it is not yet known if pecking at that device would substitute for pecking at conspecifics. Therefore, the effects of providing string devices on feather pecking in an experimental situation (Experiment 1) and on feather condition under commercial conditions (Experiment 2) were examined. In Experiment 1, 300 chicks of a high-feather pecking strain of white leghorn-type layers were housed in groups of five in litter-floor pens. The 60 pens were randomly allocated to one of five treatments: devices incorporated in the chicks’ pens continuously from 1 day of age till the end of the experiment at 57 days; devices presented for 4 h per day from 1 day of age; first presented from 22 days of age; first presented from 52 days of age; and finally, devices never presented. Feather pecking was virtually eliminated when the devices remained in the pens from 1 day of age or when they were presented for 4 h per day. Feather pecking was most pronounced among birds that had never received the device whereas its introduction at 22 or 52 days of age yielded intermediate results. This orderly pattern of more pecking at feathers when the device was added at later ages was significant (p < 0.005). In Experiment 2, 768 Lohmann LSL laying chickens were housed in rearing cages and 720 were transferred in groups of three to conventional laying cages when 16 weeks old. The birds were allocated to one of four treatments: devices present from 1 day of age; presented for 24 h every 4 weeks; continuously present from 16 weeks of age; and finally, devices never presented. At 35 weeks of age, hens with access to the device had significantly better plumage condition than those that had never received the device (p < 0.05). In conclusion, the addition of a simple string device to the pens of non-beak-trimmed high-feather-pecking birds decreased feather pecking behaviour (Experiment 1), and to the cages of non-beak-trimmed commercial layers significantly improved feather condition (Experiment 2)
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