The aim of this paper is to discuss the relationship between qualitative categories of sheep welfare and associated quantitative behavioural observations. Most scientific studies rely on quantitative measures, however to interpret those measures in terms of an animal's experience of welfare, the use of qualitative terminologies denoting various emotional states (eg fear, pain, distress) seems hard to avoid. This is especially so in cases where the same behavioural or physiological indicator could have different meanings for welfare; high levels of locomotion, for example, could indicate fear, aggression, or both. To resolve such dilemmas, scientists often resort to judging an animal's most likely state through direct observation; indeed qualitative characterisations are often intertwined with reported quantitative results. This paper reviews frequently used qualitative categories of sheep welfare and the behavioural context in which these categories are applied. Qualitative judgements of welfare tend to habitually be regarded as ‘subjective’, ie as anthropomorphic and unreliable; however from this review it appears that such judgements reflect the overall demeanour of an animal's behaviour, and as such may provide a useful empirical basis for the investigation of emotional expression in sheep. Further development of a qualitative behavioural approach may provide a more complete picture of the expressive repertoire of sheep, and enhance our understanding of ways in which these animals experience well-being or distress.

To use behaviours as indicators of stress it is important to understand their underlying causation. For a prey animal in the wild, such as a sheep, behavioural responses have evolved to evade detection and capture by predators. The behavioural responses of the wild ancestors of domestic sheep to the threat of predation are characterised predominantly by vigilance, flocking, flight to cover and behavioural inhibition once refuge has been reached. Some limited defensive behaviours are seen, mainly in females with young against small predators. Vigilance and flight distance are affected by the animal's assessment of risk and are influenced by the environment, social group size, age, sex and reproductive condition, as well as by previous experience with potential predators. Under conditions of stress, domestic sheep show similar behavioural reactions to wild sheep, although the threshold at which they are elicited may be elevated. This is particularly evident when comparing less selected hill breeds with more highly selected lowland breeds, and suggests that a continuum of responsiveness exists between wild and feral sheep, through hill breeds to the lowland sheep breeds. However, this may be confounded by the previous experience of the breeds, particularly their familiarity with humans. Behavioural and neurobiological evidence suggests that, although the behavioural response to predators (vigilance, flight) is innate, the stimuli that elicit this behavioural pattern may have a learned component. Since vigilance and flight distances are affected by the animal's perception of threat, they may be useful indices of stress in sheep and, as graded responses, give some indication of the level of threat experienced by the sheep. Thus they may indicate the amount of fear or distress experienced by the sheep and hence have the potential to be used in the assessment of welfare states.

This paper discusses the potential for using observations of behaviour to recognise distress in sheep. The term distress is used to describe situations in which an animal is likely to be suffering, and is indicating this by overt behavioural signs. Literature on the behavioural responses of sheep to procedures that induce a physiological stress response is reviewed. This approach is based on human analogy and the assumption that physiological changes can be used to differentiate between stimuli that induce an emotional response in sheep and those that do not. The degree to which the behaviour of sheep in certain situations represents, at least in part, an expression of emotional behaviour, or whether it can be fully explained as a functional response to a specific situation, is a fundamental and unresolved question in ethological and psychological studies. Therefore, the validity of compiling a list of objective common behavioural indicators of distress in sheep will be contentious. However, it is important to be able to recognise and deal with suffering, and the use of behavioural methods for the identification of distress in sheep is a practical welfare issue. There is a need for further research to identify indicators of distress in sheep, but in the meantime it would be reasonable to make the judgement that, in some circumstances, sheep that are found to be vocalising, panting, and/or showing markedly increased locomotory activity could be experiencing distress.

Chronic stress occurs when animals are unable to deal with a persistent stressor with species-typical responses, or when several stressors are present concurrently. Chronic stress is most frequently considered in intensive systems, but it may also be a welfare concern for extensively managed species, such as the sheep. Here we review behavioural and physiological responses of sheep to experimentally induced chronic stressors to determine relevant indicators of chronic stress. Neuroendocrine responses to chronic stress are difficult to interpret because initial responses are followed by an apparent normalisation. Thus, cortisol or catecholamines may be at or below pre-stress levels during chronic stress, but this varies with different stressors. Chronic stress can also affect reproductive function, impair body and wool growth and meat quality, reduce immune function, and is associated with greater parasite burdens in sheep. Chronic stress induces alterations in behaviour patterns, particularly activity and feeding, and circadian rhythms of behaviour. Stereotypic behaviours, however, are infrequent in sheep and may occur only in experimental conditions of social isolation. Behavioural and physiological data suggest that rough handling and sheepdogs may be sources of chronic stress for sheep. Social subordination and weaning also act as chronic stressors, leading to higher parasitism in these animals and a greater response to additional stressors. Lameness and parasitism are associated with physiological and behavioural responses indicating that these are severe forms of chronic stress in sheep. It is unclear whether environmental stressors, such as weather and food availability, induce chronic stress in sheep. Under-nutrition may, however, be a welfare concern through its impact on lamb survival. The existence of many sources of chronic stress in the management of sheep suggests that the welfare of this species requires more attention than it has currently received.

The provision of foraging opportunities may be a simple way of improving an animal's welfare, but this approach has been neglected for laboratory rats (Rattus norvegicus). Standard housing contains little enrichment, and food is often provided ad libitum, which may result in inactivity and obesity, especially in mature males. Foraging enrichments may offer a way to correct these deficiencies. This study compared three potential enrichments — a limited-access hopper, gnawing sticks and a foraging device — to standard housing and feeding conditions, in order to examine their effects on rat body weight, food consumption, behaviour and preferences. The subjects were 12 mature male Wistar rats. Effects were assessed from daily weighing and from video records of the rats' behaviour over 24 h periods. The rats' preferences were determined using a four-way test system in which they could choose between a standard cage and cages offering the three potential enrichments. Compared to the standard housing and feeding, the limited-access hopper had a tendency to reduce food consumption, but the time spent feeding increased. The gnawing sticks provided the rats with the opportunity to gnaw, but did not affect other behaviours or body weight. The foraging device had the benefits of reducing aggression and allowing the rats to search for and manipulate food, but resulted in significant gains in body weight. Additionally, the foraging device was the preferred feeding source. Of the four possible feeding locations, the rats spent the least amount of time in the standard cage. The foraging device provided the most benefits but requires further modification to address problems of obesity.

Theoretical models are presented of the effects of space, facilities and group size on the behaviour of chickens at high stocking densities, with relevance for all animals. The appropriateness of each model is supported by published data, although such data are scant for some important variables. Freedom of movement is analysed by taking the area of a hen as 475 cm2 and finding the number of free bird spaces left at different space allowances. This provides support for current recommendations of a maximum of seven laying hens per m2 on deep litter, but suggests that a maximum for broilers of 34 kg/m2 unacceptably restricts freedom of movement. In cages, freedom of movement increases with space allowance per hen, and, for a given space allowance, with cage and group size. Nesting behaviour is analysed for synchrony, which decreases with group size. Perching and feeding are often synchronous and the space needed for these is determined by body width. Recommendations are derived for hens in furnished cages. The main part of the cage should be as large as possible; an absolute minimum of 600 cm2 per bird is suggested, but 675 cm2 per bird is probably the minimum practical. Perch and feeder space should be provided at 14 cm or more per bird, with a possible derogation for light hybrids to 12 cm. The number of nest spaces needed varies with the number of birds, with nest spaces being 300 cm2 each. These recommendations sum to a minimum of 800 cm2 per bird for groups of eight or more, 850 cm2 for groups of four to seven, and 900 cm2 for groups of three or fewer, plus litter area. Crowding is primarily caused by limited space allowance, but for a given space allowance it is worse in small enclosures and groups.

The aim of this study was to assess the extent to which three non-invasive measures of welfare in laying hens (egg-shell quality, corticosteroid levels as measured from the birds' faeces, and behavioural preferences) were correlated over a period of five days in two groups of birds. One group had access to an enriched test area (bark chips on the floor and a tray of sprouted wheat); the other group had access to a comparably sized barren area (bare wire mesh floor). The measure of preference used was the amount of time hens spent in the test area as measured each day. It was predicted that birds with access to the less preferred environment would show higher levels of faecal corticosteroids and egg-shell anomalies. However, although the birds showed a preference for the enriched environment from Day 1, the other two measures did not follow the same pattern. Faecal corticosteroid metabolites showed an initial increase in both groups, which declined significantly by Day 4, with the ‘enriched’ birds in fact showing a trend for higher levels than the ‘barren’ birds. Shell thickness also showed a change over the five days, but with a different time course: declining to a minimal level on Day 3 and then rising again by Day 5. No measure of shell quality was significantly different between the two environments, but there was a trend for changes in shell thickness to be more pronounced in eggs from enriched birds. The results indicate the caution that needs to be exercised in using shell quality or corticosteroid measurements in isolation from assessments of what the animals themselves prefer.

The aim of this study was to assess optimal temperature ranges for fattening pigs of different weights kept in pens with partially slatted floors. We examined the behavioural and adrenocortical responses of pigs of different weights (25–35 kg, 50–70 kg, and >85 kg) to a wide range of ambient temperatures (2–29°C). On three days of each experimental period, we took saliva samples for the analysis of cortisol concentration, and recorded lying behaviour from 0800–0600h. Behavioural and cortisol parameters were analysed using linear mixed effects models. Optimal temperature ranges for the three weight-classes were calculated using logistic regression. Pigs chose different areas for resting depending on ambient temperature. With increasing temperature, pigs used the dung area more often and lay more often without contact with pen mates. Compared to lighter pigs, heavier pigs lay without contact with pen mates at lower temperatures. In general, lying without contact occurred at temperatures 5–7°C lower than lying in the dung area. Huddling increased with decreasing temperature, and, with increasing weight, pigs showed huddling at lower temperatures. There was a significant increase in cortisol levels at high ambient temperatures in pigs >85 kg. In pens with partially slatted floors, the results indicate temperature ranges within the thermal tolerance of pigs to be 19–21°C for pigs weighing 25–35 kg (lying area of 0.46 m2/pig), 10–17°C for pigs between 50–70 kg and 5–17°C for pigs >85 kg (both weights: lying area of 0.67 m2/pig).

We report on the efficacy of body weight change as a measure of trapping and handling stress in two species of wild small mammal: bank voles (Clethrionomys glareolus) and wood mice (Apodemus sylvaticus). We tested two hypotheses: (1) that weight change after capture and handling is related to the intensity of the trapping and handling regime, and (2) that weight change after an intensive handling regime is related to an individual's current pattern of energy expenditure. Trapped wood mice that were subjected to intensive handling (intensive stressor) lost more weight than did animals that were handled minimally (less intensive stressor), but this was not the case for bank voles. Patterns and factors related to body weight change in response to intensive handling also differed between the two species: heavier and non-breeding bank voles were more likely to lose weight, but this was not true for wood mice, and none of the factors we measured was found to affect weight loss in this species. Our results were broadly consistent with the predictions of the biological cost hypothesis. We discuss the limitations and benefits of weight loss as a measure of stress.

The objective of this project was to collect scientific data to assist in the development of guidelines for the humane relocation of threatened and endangered arboreal non-human primate species. A troop of 31 Lowland Sykes monkeys (Cercopithecus mitis albotorquatus) was habituated to fruit bait for capture in a village and relocation to a previously selected suitable site in a protected forest reserve approximately 30 km away. Sixty-five percent (n = 20) of the animals were captured and relocated. This subgroup comprised one adult male, eight adult females, two subadult females, three juvenile males, four juvenile females and two infant males. Although the relocated group originated from one single group, post-translocation telemetry signals demonstrated that it split into two groups, which established themselves approximately 2–4 km apart in their new territory; the adult male eventually became solitary. The factors of importance for the successful capture and relocation of forest primates were found to include: proper understanding of troop home-range utilisation and of social bond organisation within the troop, method and period of habituation, method of release, suitability of the new habitat with respect to the ecological niche requirements of the species in question, and the period of post-relocation monitoring.

Wild badgers (Meles meles) in Wytham woods, Oxfordshire, are routinely trapped, transported to a central field laboratory, studied and released as part of an on-going population study. These procedures have been carefully developed to minimise impact on the badgers' welfare; however they are potentially stressful, and, as part of our on-going welfare refinements, and our exploration to develop methods for quantifying stress in wild mammals, we studied the effects of transport stress on neutrophil activation in wild trapped badgers. Blood samples were obtained from 28 badgers. We compared three transport regimes: transported (n = 9), transported and rested for at least 30 mins (n = 11), and not transported (n = 8). Total and differential white cell counts were carried out and neutrophil activation was measured by the nitroblue tetrazolium test. Our goal was primarily to validate neutrophil activity as an indicator of stress, on the basis that the transport treatment was expected to be more stressful than the non-transport treatment. There were significant increases in % activated circulating neutrophils in response to transport. This study supports the proposition that stress affects circulating neutrophil numbers and the state of their activation, as determined by the nitroblue tetrazolium reduction assay, and therefore adds weight to the idea that neutrophil activation is a potential measure of stress in wild animals.

Increasingly, perches for laying hens are being made from metals and plastics. There is nothing in the literature regarding how easily birds jump between perches of different materials, or how their ability to do so changes with faecal contamination of the perches. Forty-four medium hybrid brown hens negotiated perches of wood (5 cm × 5 cm, rounded edges), metal (half-round section, diameter 4 cm) or poly-vinyl-chloride (PVC: circular section, diameter 4 cm), which were either clean or dirty (poultry manure 0.5–1.0 cm deep). The time to jump to the destination perch (0.75 m from the start perch), number of squats (pre-jumping behaviour), slips, failures to jump (in 300 s) and crashes were recorded. Compared to wood and metal perches, birds took significantly longer to jump from PVC perches when they were clean, but there was no difference when the perches were dirty. Birds slipped significantly more on clean metal or PVC perches compared to clean wood perches. The birds took significantly longer to jump from metal or wooden perches when they were dirty compared to when they were clean. These data may suggest that PVC is not a suitable material for perches. Slipperiness is important. The birds apparently found the metal and PVC perch more slippery than the wooden perch, although the metal perch did not cause the birds to delay jumping. A slippery perch may deter the birds from attempting to jump. Manure on the perches reduced the slipperiness of the metal and PVC perches. Once perches become dirty, any welfare issues concerning the risk of injury from slippery perches cease to be as important as the potential slipperiness of the manure itself.

This study explored the influence of five toys (squeaky ball, non-squeaky ball, Nylabone chew, tug rope and Boomer ball) on the behaviour of 32 adult dogs housed in a rescue shelter. The dogs were exposed to each toy separately for six days, with an intervening period of one day between toys. The dogs' location in their kennels (front or back), activity (moving, standing, sitting or resting) and vocalisation (barking, quiet or other) were recorded over 4 h at 10 min intervals on Days 1, 3 and 5 during a control condition (no toy present) and during five experimental (toy) conditions. Whether or not the dogs were observed playing with the toys during the experimental conditions was also recorded. The dogs spent relatively little (<8%) of the overall observation time playing with the toys. The toys elicited varying degrees of interest, with dogs showing a preference for the Nylabone chew over the other toys. The dogs' interest in the toys waned over time, but the speed of habituation to the Nylabone chew was slower than to any of the other toys. The dogs' activity was significantly related to toy condition: dogs spent more time moving and less time standing during the Nylabone chew, squeaky ball and non-squeaky ball conditions than during any of the other conditions. It is suggested that the welfare of kennelled dogs may be slightly enhanced by the addition of suitable toys to their kennels. It is advised, however, that toys are rotated to encourage exploration and reduce habituation. The provision of other forms of environmental enrichment is also recommended.