Six pairs of steers were allowed to choose between two types of floors in a paired choice test. The four floors tested were a fully slatted floor, a fully slatted floor covered with rubber mats, a solid floor with sawdust bedding, and a solid floor with straw bedding. All combinations of floor types were tested and the choices were repeated eight times, using naïve animals. The animals were allowed 17 days to habituate, and on days 18-21 their behaviour was recorded by video for 72 hours. Straw was the most preferred floor type, followed by sawdust, then mats, and finally slats. During a second test period, rubber mats were compared with rubber strips, and no significant preferences were found.

The possibility of lessening the adverse welfare impact of artificial rearing was assessed in thirty Comisana lambs under conditions of ad libitum feeding. The lambs were assigned to a control dam-suckled group (DS) or to one of two test groups, each consisting of 10 animals. 18-24h after parturition, test lambs were separated from their dams: during the first postseparation week 10 subjects (EM) were offered ewe milk and the other 10 (MX) a 50:50 mix of ewe milk and a milk substitute. An artificial feeding system, to which the test lambs had free access, was filled with milk twice daily. After the first week, a transition from EM or MX to 100 per cent (reconstituted) milk substitute was carried out over 3 days in both test groups, gradually reducing the proportion of ewe's milk. In vivo cell-mediated immune response of lambs to phytohemagglutinin percutaneous injection were evaluated at 5, 15 and 25 days of age. At 10 and 20 days of age, all lambs were subjected to 15min isolation tests, during which latency to move, duration of movement and number of bleats were recorded. Blood samples were collected immediately before the test and 15 and 60min after, in order to assess the effect of differential rearing on the Cortisol response of animals at different ages. In addition, the weight gain of lambs was recorded during the first 35 days of age at weekly intervals. Latency to move and duration of movement were not significantly affected by the experimental treatment, whereas the number of bleats was higher (P < 0.001) in dam-suckled lambs compared to test lambs at both 10 and 20 days of age. Neither immune response nor Cortisol levels were affected by milk source. Although weight gain increased with increasing amounts of ewe's milk in the diet, the overall differences between the three groups were small and not significant. These findings suggest that the provision of ewe milk or a mix of ewe milk and a milk substitute during the first post-separation week can be a suitable strategy to sustain the welfare and production performance in the artificially reared lamb.

Many captive giraffes perform oral stereotypies, in particular tongue-playing, licking of objects (including conspecifics) and vacuum chewing. Typically, the diet of these large ruminants in captivity consists mostly of food concentrates, which are consumed rapidly and do not provide stimulation for their long, prehensile tongues. In the wild, browsing requires extensive use of this organ but in captivity material upon which to browse is limited. Consequently, vacuum activities, such as mock leaf-feeding behaviour, and stereotypies may develop. Rumination is also a major component of a giraffe's behavioural repertoire. It is essential for proper digestion, but may also be connected with non-REM sleep. Inadequate opportunities for rumination may also contribute to the development of oral stereotypies. In this study of captive giraffes, we examined the effect of increasing dietary fibre on the time spent ruminating and feeding and the extent to which oral stereotypies were performed. Two giraffes of different age, sex and sub-species were studied at Paignton Zoo Environmental Park. Dietary fibre was increased by the addition of coarse meadow hay to their existing diet. Following the addition of hay, time spent feeding did not change significantly but there was a significant increase in the time spent ruminating and a significant reduction in time spent performing oral stereotypies by both giraffes, suggesting that oral stereotypies may be connected with rumination rather than feeding. Stereotypic behaviour is generally accepted to be an indicator of sub-optimal welfare. Thus, the reduction in this behaviour by the simple addition of coarse fibre to the diet can be interpreted as enhancing the welfare of these animals.

Recent scientific findings indicate that consciousness is a fundamental biological adaptation. The known brain correlates of consciousness appear to be phylogenetically ancient, going back at least to early mammals. In all mammals, alertness and sensory consciousness are required for the goal-directed behaviours that make species survival and reproduction possible. In all mammals, the anatomy, neurochemistry and electrical activity of the brain in alert states show striking similarities.

After more than seven decades of cumulative discoveries about waking and sensory consciousness, we have not yet found any fundamental differences between humans and other mammals. Species differences such as the size of neocortex seem to be irrelevant to the existence of alertness and sensory consciousness, though different mammals obviously specialize in different kinds of sensory, cognitive and motor abilities.

Sceptics sometimes claim that objective evidence for consciousness tells us little about subjective experience, such as the experience of conscious pain. Scientifically, however, plausible inferences are routinely based on reliable and consistent patterns of evidence. In other humans, we invariably infer subjective experiences from objective behavioural and brain evidence - if someone yells ‘Ouch!’ after striking a finger with a hammer, we infer that they feel pain. The brain and behavioural evidence for subjective consciousness is essentially identical in humans and other mammals. On the weight of the objective evidence, therefore, subjective experience would seem to be equally plausible in all species with human-like brains and behaviour. Either we deny this experience to other humans (which is rarely done) or, to be consistent, we must also attribute it to other species that meet the same objective standards. It seems that the burden of proof for the absence of subjectivity in mammals should be placed on the sceptics.

The captive environment is often barren, predictable and under-stimulating so that the behavioural needs of animals in captivity may be thwarted. The welfare of animals may be compromised, which can result in the expression of abnormal behaviours. Stereotypic behaviours, such as the circling or pacing behaviour observed in captive pinnipeds, may become apparent. A simple, cheap and effective method of adding complexity to a captive environment is the use of environmental enrichment techniques. A number of enrichment devices were used in this study, focusing primarily on occupying more time in feeding/foraging behaviours of common seals, Phoca vitulina. The performance of stereotypic circling behaviour was significantly reduced during the enrichment period, suggesting it had improved the welfare of all the animals in this study.

Biotelemetry is a useful tool for the simultaneous measurement of several physiological and behavioural parameters in non-restrained, freely moving animals. However, the weight and volume of the implanted intra-abdominal transmitter may cause discomfort. The aim of this study was to assess body weight and behaviour of BALB/c and 129/Sv mice after implantation of an intra-abdominal transmitter. In order to measure more detailed behaviour, the automated behaviour observation analysis system (LABORAS™) was used. During the first days after surgery, body weight and the behaviours of climbing, locomotion and eating were found to decrease in both strains, whereas grooming and immobility increased. These changes were more pronounced in the transmitter animals than in the sham operated animals, however, indicating a temporary impairment in well-being. Within two weeks after surgery, the animals seemed to have fully recovered.

Deflighting is used to prevent large captive birds from escaping by limiting their ability to fly. This practice deprives birds of this normal behaviour, but can allow them to express other behaviours that would be suppressed if they were confined to cages or aviaries. The potential negative welfare issues associated with deflighting include the stress of capture and restraint, pain and discomfort associated with the procedure and during recovery, risk of post-operative infections, risk of neuroma formation which could lead to pain, and loss of the ability to fly. The potential practical and welfare advantages of deflighting include a reduction in the need to closely confine or cage birds to prevent them from escaping, and deflighting may be the only way of keeping particular birds in an open situation for display, such as in parks or zoos. In these respects, there must be a balance between the requirement for this practice and the welfare compromises it introduces for birds. By outlining temporary and permanent methods and the complications involved, the following review highlights potential welfare problems and discusses ways of avoiding them. It also evaluates the necessity of deflighting and the need for careful risk assessment.

The common practice of preventing equine stereotypic behaviour in the UK may be of concern, from a welfare perspective, if these behaviours constitute a coping response to a suboptimal environment. The aim of this study was to assess the putative function of these behaviours by measuring behavioural and physiological parameters i) before and after stereotypy prevention; ii) before and after stereotypy performance; and iii) in response to opiate antagonist (naloxone) administration.

The crib-strap significantly (P = 0.05) elevated mean plasma Cortisol levels in crib-biting horses; a similar, although not significant trend (P = 0.07) was also observed for the weaving group during the anti-weave bar treatment. Both crib-strap and anti-weave bar significantly (P < 0.05) elevated plasma Cortisol levels in the control horses. Although the latter result prevented a definite conclusion being drawn about the function of equine stereotypies, the results did indicate that the use of the crib-strap and anti-weave bar is stressful to the horse.

Plasma Cortisol level was significantly (P = 0.04) higher immediately prior to the onset of stereotypy followed by a significant reduction post-stereotypy. This suggested that both crib-biting and weaving have a coping function to reduce stress levels in the animal.

Naloxone significantly reduced crib-biting by 84 per cent (P = 0.05) but it did not reduce weaving behaviour, indicating that crib-biting is a reward behaviour. However, resting behaviour was also significantly (P = 0.02) increased in crib-biting horses, suggesting that the stereotypy reduction was due to a sedative effect of the opiate antagonist. The latter was not measured, however, in control or weaving animals, and thus may be interpreted differently. The welfare implications of these results are discussed.

There are several examples from human neuropsychology of the intact preservation of processes and capacities in the absence of conscious awareness by the patients. These include loss of visual awareness (blindsight), episodic memory (amnesic syndrome), attention (unilateral neglect) and language (aphasia). The implication of these and other clinical phenomena is that descriptions of ongoing behaviour are necessary but quite insufficient for making inferences about conscious awareness, because even quite ‘high level’ behaviour can be run off in the absence of awareness. A commentary, or independent off-line response, is a prerequisite for determining whether the subject is consciously aware. Whether or not the commentary allows an inference about awareness in animals rests ultimately on an argument from analogy, just as is the case when we make judgements about fellow humans. But when parallel disjunctions between on-line behaviour and off-line classifications are found for both human and infrahuman subjects, as is demonstrable for blindsight and amnesia, not only do they bolster inferences about common neural mechanisms, but they strengthen inferences for analogous processing and hence for conscious experience.

Both the presence of slurry and dark conditions may deter dairy cows from using passageways in cubicle accommodation, thus restricting movement and normal behaviour. We attempted to train seven dairy cows to recognize the quantity of reward offered in a transparent tube containing molasses in a Y-maze. Only one cow failed to consistently select the aisle containing the larger reward. The cows were then individually offered the choice of traversing either a passageway with a 5cm-depth of cow excreta or a clean, dry passageway to collect their rewards. The quantity of the rewards on the two sides was varied between zero and 400ml of molasses to determine the price that the cows were prepared to pay for entering the aisle with excreta. Only two of the seven cows showed a clear avoidance of the passageway with excreta. There was a tendency (P < 0.1) for the cows to avoid the passageway with excreta only when it contained no reward and the clean passageway contained a reward of 400ml molasses. Otherwise, there was no clear avoidance of the passageway with excreta. We also investigated whether cows preferred to enter a lighted or unlighted passageway. All the cows, except one, showed a strong avoidance of the dark passage, even when it contained the largest reward and the lighted passage contained no reward. We conclude that dairy cows demonstrate only mild avoidance of passageways with excreta but strongly avoid passageways without lighting. Therefore, we suggest that passageways for dairy cows should be lit at all times.

One commonly used method of managing confiscated wild primates in Latin American countries is to release rehabilitated individuals back to their natural habitats. However, little information has been collected from confiscated animal releases, so no clear guidelines have been developed to measure the success of this type of procedure. In most countries, the collection of critical post-release data is too costly and time-consuming for it to be incorporated into the routine procedures of institutions managing confiscated fauna. Therefore, this project was carried out in conditions similar to those of other Colombian and Latin American rehabilitation centres. A group of eight confiscated and rehabilitated brown capuchin monkeys (Cebus apella) was released in Los Llanos Orientales in Colombia, and monitored for 6.5 months to determine their adaptation and survival after release. Results were analysed according to how the animals adapted to their new environment in terms of foraging, feeding, locomotion, sleeping, social interactions between the group and with other animals and species, prédation, orientation, and establishment of a territory. The results show that the short-term adaptation and survival of the group 6.5 months after release was successful. Five of the eight animals remained together, two separated, and only one was lost during the first month. Implications for animal well-being are discussed.

Textbook recommendations for gavaging rats vary between 1-5 ml for an adult rat. Rats weighing either 130 g or 250 g were gavaged with varying dosages of barium sulphate (BaSO4). After dosing, radiographs were taken at 0, 15 and 60 min. Animals showing a section of the small intestine totally filled with BaSO4 were scored as displaying spontaneous release. Other rats of the same sizes were gavaged with similar doses and subsequently tested in an open-field arena for behavioural abnormalities that might indicate stress or pain resulting from the procedure. Body temperature before and after treatment was recorded using microchip transponders. None of the 250 g rats in the 1 ml dosage group showed spontaneous release through the pyloric sphincter. In the 2 ml and 4 ml dosage groups, only one out of five animals showed spontaneous release. In the 6 ml dosage group, half of the animals showed spontaneous release. In the 8 ml and 10 ml dosage groups, five out of six and four out of five, respectively, showed spontaneous release. If doses were higher than 12 ml, no animal was able to keep all of the BaSO4 in its stomach. In the rats weighing 130 g, the 3 ml dosage group showed only one out of four rats with spontaneous release, whereas in the 5 ml and 7 ml dosage groups, all animals showed spontaneous release. After 15 min, all of the rats in both weight groups showed BaSO4 in the duodenum. Ambulation, rearing up onto the hind legs and defecation, as well as body temperature immediately after dosing, correlated very strongly with the dose (ml kg−1); increasing the dose resulted in reduced ambulation, rearing, defecation and body temperature. However, 10 min after performance of the open-field test, neither body temperature, serum corticosterone nor serum glucose showed any correlation with dose. This study indicates that high doses (ie doses up to 10 ml for a 250 g rat) might be safe to use; however, if an adverse impact on the rat is to be avoided, use of much lower doses should be considered—for example, doses that do not enforce opening of the pyloric sphincter in any rat. This would be less than 4 ml kg−1 in a 250 g rat.

This paper will try to answer the question of whether animals can suffer.

My aim is, firstly, to discuss whether or not an irreflexive animal consciousness could experience suffering. I do this because there are authors who assume such a consciousness in animals. The second part of this contribution concerns the question of the cognitive and neural prerequisites which have to be present in order to give consciousness, or the suffering experience, a positive fitness value. Further, I analyse for which animals these brain structures and cognitive capacities have been described, since consciousness and suffering can only be expected in these animals.

In order to answer the questions, several assumptions had to be made. If the assumptions are correct than the results of the various analyses demonstrate that: i) an irreflexive consciousness is unable to experience suffering; and ii) animal suffering may, for the time being, only be expected in the anthropoid apes. However, there is an important difference between the registration of pain as a stimulus, which does not induce feelings of suffering, and the experience of pain as an emotion, which does induce suffering. According to the arguments presented in this contribution, the experience of pain as a stimulus could be expected in far more species than anthropoid apes alone.

It is believed that environmental enrichment techniques can play an important part in creating suitable captive environments for horses. There has, however, been little scientific investigation into the effectiveness of ‘stable-toys’ which claim to reduce the performance of equine stereotypies. This study investigated the effect of a foraging device known as ‘The Equiball™’ on equine stereotypies. Six horses were given their evening feed in an Equiball, and the occurence of stereotypic behaviour recorded using scan sampling of video observations. Pre-enrichment, horses spent a mean (± SD) of 5.27 ± 8.17 per cent of their time in the stable performing stereotypies; and significant individual variation in mean time performing stereotypic behaviour was found (P < 0.05). Several peaks in stereotypy over the day were found, the two main ones corresponding to the times before feeding. A reduction in stereotypic behaviour in five horses, and a small increase in stereotypic behaviour in one horse was observed during enrichment. During enrichment, there was an overall trend for stereotypic behaviour to decrease (P < 0.1). When used in conjunction with other measures such as behaviour therapy, companionship, increased exercise, and so on, the Equiball may help to create an environment less likely to lead to the development of stereotypic behaviours.

This experiment examines the consequences and welfare implications of the introduction of new rats to established (resident) caged laboratory rat groups. The effects on investigatory and aggressive behaviours of the established and the newly introduced rats were measured. The aggressive status within each established resident group was known prior to the introduction; the status of each intruder rat was also known. Single-sex groups of both male and female residents and intruders were studied. Two important conclusions arise from the results of the experiment. First, contrary to reports in a number of publications, there were no effects of male resident social status on their investigatory or aggressive behaviour towards male intruder rats. There was, however, a significant effect of social status among female residents on their investigatory behaviour towards intruders; unexpectedly, it was the subordinates followed by the dominant animals that showed the highest investigatory response. Second, aggression by intruders of both sexes depended upon their social status in their resident group. In the case of male intruders, aggressive behaviour towards residents was a reflection of their previous social status irrespective of how much aggression they received from residents. Among females, a similar pattern emerged, with the dominant females initiating the most aggression; however, this behaviour was dependent upon how much aggression was received from residents and on the resident’s social status, with resident subordinates and dominants responding with the most aggressive behaviour. The results are interpreted in terms of putative competitive strategies adopted by rats in a confined (cage) environment, and their welfare implications are discussed.

The attempt to provide a firm scientific basis for understanding consciousness is now in full swing, with special contributions from two areas. One is experimental: brain imaging is providing ever increasing detail of the brain structures used by humans (and other animals) as they solve a variety of tasks, including those of higher cognition. The other is theoretical: the discipline of neural networks is allowing models of these cognitive processes to be constructed and tested against the available data. In particular, a control framework can be created to give a global view of the brain. The highest cognitive process, that of consciousness, is naturally a target for such experimentation and modelling. This paper reviews available data and related models leading to the central representation, which involves particular brain regions and functional processing. Principles of consciousness, which have great relevance to the question in the title, are thereby deduced. The requisite neuronal systems needed to provide animal experience, and the problem of assessing the quality and quantity of such experience, will then be considered. In conclusion, animal consciousness is seen to exist broadly across those species with the requisite control structures; the level of pain and other sensations depends in an increasingly well-defined manner on the complexity of the cerebral apparatus.

A new, external non-invasive telemetric heart rate (HR) monitoring system was evaluated on eight wapiti, Cervus elaphus canadensis, yearlings in July and August 1996. The assembly consisted of a leather girth strap, onto which a HR transmitter and a customized carriage bolt electrode system were fixed. To prevent the girth strap from rotating on the animal, it was secured with adjustable nylon straps extending anteriorly between the forelegs up to an adjustable neck collar. In preliminary testing, audible tones were received during 99 per cent (n = 902) of the 15s intervals when the animals were active, but only during 33 per cent (n = 156) when they were bedded. After 2 weeks, the equipment remained functional (and was removed); the effective signal range was consistently beyond 500m. This HR monitoring system is easy to attach externally, obviates complications from surgery, and provides coverage over an extended range.

The monitoring system offers a reliable, humane and inexpensive method for short-term measurement of HR in captive or wild ungulates. Further tests may reveal a potential for long-term application. The ability to measure physiological responses under different management regimes can aid ungulate farmers in selecting optimal herd sizes and social structures for their animals; and in developing superior housing, enclosure designs, handling and transport methods. This improves the animals’ welfare, and ultimately leads to an increase in animal growth and herd productivity. In addition, information about heart rates can help wildlife managers to improve their management strategies, by gaining an understanding of the energy expenditure associated with various activities and environmental influences.

Fur-farming is a politically sensitive issue today. Therefore, discussions on the welfare situation of commercially farmed fur animals may be particularly valuable. The aim of this Short Communication is to address some issues, in addition to those covered in the review of Nimon and Broom on the welfare of farmed mink (Animal Welfare 1999, 8: 205-228), that may have received too little attention. This Short Communication addresses domestication and animal welfare, indispensable resources and behaviours of farmed mink, and the use of negative and positive indicators of welfare in research on farmed mink.

Many studies on group-housing of laboratory rabbits to date have focused on management aspects and economic implications. Our aim here is to provide behavioural background information for future investigations focusing on behavioural and welfare aspects of group-housing. In the present study, we established the behavioural repertoire of female laboratory rabbits kept in single-sex groups in enriched floor-pens. Thirty-six adult does of common laboratory breeds were kept in groups of four in enriched floor-pens. Behavioural observations were carried out over a period of 30 months with a total observation time of 21 h per group and 4.2 h per focal animal. Observations took place at natural dusk and dawn and lasted for 120 or 180 min per group. Most of the behavioural elements in the repertoire of mixed-sex wild and domestic rabbits were also observed here in single-sex groups of laboratory does. However, in the absence of males, sexual behaviours were directed towards other females and no maternal behaviours, other than nest building at the end of pseudopregnancies, were exhibited. Attention is drawn to differences between the behavioural repertoire reported here and that of singly caged laboratory rabbits.