Female laboratory rats (Rattus norvegicus; Wistar, Alderley Park) were housed as singletons or groups of three in units of two cages. Units were divided by different types of barrier which allowed varying degrees of social contact across the barrier. Singletons were established either with another singleton on the other side of the barrier or with a group of three as neighbours. Single-housing among females had markedly less effect on time budgeting and pathophysiological measures than among males in a similar, earlier study. In particular, singletons showed a less marked increase in self-directed behaviours, particularly tail chasing, and a smaller reduction in undirected movement around the cage. The smaller reduction in mobility may reflect a greater tendency for singly housed females to attempt escape. Females generally showed much higher levels of escape-oriented behaviours than males and up to a threefold increase in such behaviours when housed singly. Differences in time budgeting and in the apparent significance of social separation between the sexes can be interpreted in terms of differences in socio-sexual strategy and potential mating opportunity, with singleton males responding to their cage as a territory, but singleton females seeking to re-establish social contact. Such an interpretation is consistent with the effects of barrier type on behaviour in singleton females, in which time spent in escape-oriented behaviours reflected the extent to which the barrier facilitated, or frustrated, contact with neighbours.

Male laboratory rats (Rattus norvegicus; Wistar, Alderley Park) were housed as singletons or groups of three in units of two joined, but divided cages. Units were divided by different types of barrier that allowed different degrees of social contact across the barrier. Singletons were established either with another singleton as a neighbour on the other side of the barrier, or with a group of three as neighbours. Relative to group-housed animals, singly-housed rats showed reduced activity and a greater incidence of self-directed behaviours and behaviours apparently related to escape or seeking social information. Pathophysiological evidence was consistent with Baenninger's (1967) suggestion that tail manipulation in singletons is a surrogate social response, but was also consistent with an overall increase in self-directed activity, reflecting elasticity in time budgeting. Variation in the degree of increase in self-directed activity among singletons and the negative correlation between self-directed activity and organ pathology may have reflected differences in the ability of individuals to avoid an activity limbo. While reduced corticosterone concentration and organ pathology compared with grouped rats implied that separation may remove social stress, responses to contact with neighbours, and correlations between behaviours and organ pathology suggested that rats may actively seek social interaction. Broad differences in stress responses between single and grouped housing conditions may therefore be an inadequate yardstick to the animals’ welfare. However, exposure to neighbours reduced the aggressiveness of singly-housed males when they were eventually introduced into an unfamiliar group, suggesting that a degree of exposure to neighbours (separation, but not isolation) may have some welfare benefits for laboratory-housed rats, depending on procedures.

To assess the validity of using wild behavioural data as a welfare indicator for zoo animals, the time budgets of 19 captive giraffe (Giraffa camelopardalis), from four zoos were compared with the time budgets of wild giraffe from Hwange National Park, Zimbabwe. Differences were shown to exist between the behaviour of wild and captive giraffe. However, only the duration of lying differed significantly across zoos. Correlations demonstrated that both enclosure size and feed restriction affected the locomotor activity of giraffe. An attempt to quantify observer influence upon the behaviour of wild giraffe was made. Different methods of observation were shown to significantly affect the time budget established. The extent to which wild giraffe behaviour can be used as a welfare indicator for captive conspecifics is discussed, as are the problems inherent in such a study. The difficulties in constructing an alternative welfare measure using prevalence to veterinary problems, are briefly considered. Methods by which captive giraffe welfare can be improved are discussed, particularly concerning the provision of browse to allow more natural feeding patterns to be established.

Adrenocortical activity and time budgets in a robotic milking system in two variants of cow traffic (partially forced, free) were compared with a conventional milking system, focusing on the relationships between adrenocortical activity, time budgets, and social rank of the cows. Both groups were housed in identical conditions and consisted of 30 cows each. Within each experiment, direct observations of social behaviour and 24-hour video recordings were conducted during six two-day blocks. We calculated the dominance value and the time budget (‘lying’, ‘feeding’, ‘other activity’) of each cow. Faeces from each cow were collected to determine the concentration of cortisol metabolites (CCM) as an indicator of baseline adrenocortical activity and possible chronic stress. Analysis of CCM and time budgets did not indicate any adverse effects of the robotic milking system, with one exception: under partially-forced cow traffic, cows of low social rank had longer waiting times in front of the robot. Considering the fact that the number of cows milked by the robot was less than half of that recommended by the manufacturers, our results do not exclude the possibility that a higher stocking rate may lead to further adverse effects.

Previous research on activity patterns of the elderly has relied on survey and interview methods which have depended on special measures and the long term memory of the respondents. This paper examines the use of time budgets in studying changing activity patterns across the life span. The independent variables of interest in this analysu were age, sex, marital status, education, and whether or not the individual lives alone. The dependent variable was the activity patterns of the individual. Results indicate that only age, of the factors considered here, endured significance across all comparisons.

The frugivorous phyllostomid bat Carollia perspicillata is closely associated with specific fruits which are found and picked in flight, then eaten at a feeding roost. Each fruit eaten corresponds to a single flight. An apparatus designed for this study permits the simultancous tracking of 10 bats equipped with double rhythm transmitters (slow rate corresponding to resting position and rapid rate to flying bouts). (1) The number of flights, (2) the percentage time spent flying and (3) the range of activity were recorded for different categories of animals during two periods of fruit production. Heavier males displayed high activity, while other males, non-breeding females and females in early pregnancy displayed a similar pattern of flying behaviour. Full-term pregnant females and lactating females performed almost as many flying bouts as non-reproductive females, but these flights were much shorter. This unexpected feeding strategy can be interpreted as a means of shifting energy to reproductive effort from exploratory behaviour (non-breeding females performed longer flights which combine the survey of environment and the fruit collection). This strategy, based upon the optimization of flying bouts, is in contrast to those of non-flying mammals and probably is only compatible with periods of high food production.

Acoustic monitoring and radio-tracking were used to study the nocturnal activity of adult female Indiana bats Myotis sodalis at a maternity site in Michigan, U.S.A. Pregnant bats did not use the day roost at night, but lactating females returned 2–4 times/night for 32±7 (SE) min/visit, presumably to feed their young. Both pregnant and lactating females night roosted as solitary individuals in trees within their foraging areas; night roosting occurred 0–6 times/night for 14±1 min each time. Bats foraged for most of the night, with the total duration of flight equalling 375±16 min/night. The bats used 13 different foraging areas that were located 0.5–4.2 km from the day roost. Bats did not fly over open fields but travelled along wooded corridors, even though such behaviour increased commuting distance by 55±11%. Current models of habitat suitability for this endangered species should be modified, taking into account the use of wooded commuting corridors and the large home range of these bats.

The timing and duration of activity and foraging behaviour of mahogany gliders Petaurus gracilis was studied every 2 months over 2 years by direct observation. The amount of time spent active each night throughout the year ranged from 8 to 10.1 h (or 63–80% of the dark phase) and did not change significantly between the wet and dry seasons. Although gliders generally had one continuous period of activity, they were observed on eight occasions to return to their dens during the night for a mean of 85 min, with a mean entrance and exit being 22:59 and 00:25, respectively. The amount of time spent foraging (i.e. feeding and travelling) ranged from 40% of the time outside the den in January to 77% in September. The overall mean was 61.1%, with the remainder of the night spent either stationary (mean 24.3%), grooming (mean 11.8%), in the den and then re-emerging (mean 2.5%) or vocalizing (mean 0.3%). Activity comprised mostly the behaviours associated with foraging: feeding (44.9%), climbing (13.2%) and gliding (3.0%). The amount of time spent active and feeding was similar to that observed for other petaurid marsupials such as yellow-bellied glider P. australis, sugar glider P. breviceps and squirrel glider P. norfolcensis. There is a general relationship between diet, body size and amount of time spent feeding among the exudivorous gliders and folivorous possums, with feeding time increasing with increasing body mass in exudivorous possums and decreasing with increasing body mass in folivorous possums.