Trade-off between floor level and floor material in farmed silver foxes

Farmed silver foxes (Vulpes vulpes) were allowed to balance their known preference for an elevated floor against their presumed preference for a sand floor. In Experiment 1, foxes had to choose between two identical cages, connected with an opening. One cage had a wire floor and the other had a sand floor, but the cages either were on the same (low or elevated) or on different levels (one cage 40 cm higher than the other). In Experiment 2, the cage pairs were connected with a 1.2 m long wire-mesh tunnel, one cage was always on a higher level (50 cm) than the other. In Experiment 1, foxes always preferred the sand floor during their active time. They also preferred the sand floor for resting, if it was on the same level as wire floor, but did not show any genuine preference if the floors were on different levels. In Experiment 2, foxes never preferred the lower floor. They preferred the elevated sand floor for activity and the elevated wire floor for lying. When two floors were identical they preferred the elevated one. Their rest consisted of 11-22 bouts, a major part of these being spent in the preferred cage. They also preferred a previous lying site to a new one, often exclusively and independently of floor material. In Experiment 1 foxes preferred the sand floor whereas in Experiment 2 they preferred the elevated floor indicating that the ability of a trade-off situation to rank resources depends on the method it is inflicted.     

Position of operant cost affects blue foxes’ time budget between sand floor and mesh floor

The aim of the study was to assess whether positioning of the operant cost would affect blue foxes’ (Vulpes lagopus) behaviour and time budget between a mesh floor and sand floor. We built fourteen test apparatuses, six consisting of two fox cages with a mesh floor in both cages and eight with a mesh floor in one cage and a sand floor in the other cage. A cost could be imposed to pass through one-way doors between the cages. The effect of changing the cost to move from the mesh floor to the sand floor or from the sand floor to the mesh floor or between the two mesh floors was examined in 28 juvenile male blue foxes. The foxes’ time allocation between the cages was recorded for four different costs. The foxes’ behaviour was analysed in more detail at the lowest and highest costs. The visit duration increased considerably when leaving the cage became costly, but did not markedly change when entering was costly. The foxes spent less time on the sand floor than on the mesh floor. The foxes preferred to rest on the mesh floor, but rested also on the sand floor when there was a cost associated with leaving the sand floor. The sand floor stimulated digging, rooting and play. In conclusion, both positioning of the cost and the floor material affected blue foxes’ time budget between the two cages.     

Complex housing environment for farmed blue foxes (Vulpes lagopus): use of various resources

The present study was designed to measure the use of various, simultaneously available resources in a complex housing environment in juvenile blue foxes. Twelve blue fox sibling (male–female) pairs were housed in two-section experimental cages from the age of 8 weeks until the age of 7 months (from June to December). Each experimental cage was furnished with two platforms, a nest box, a sand box and a wooden block. This housing set-up provided the foxes with social contact, and an opportunity for oral manipulation, scratching and nesting, as well as the choice of staying on a solid floor material or on an elevated location. The foxes’ behaviour was recorded at three time points during autumn (September, November and December). The foxes used all available resources. The most utilised resource was the nest box, possibly because it could be utilised in several ways (as a shelter, an elevated location, an object for scratching and for oral manipulation). The foxes also stayed more in the cage section containing the nest box than in the cage section containing a sand box. The foxes rested much on the cage floor, but they also used the interior of the nest box and elevated locations for resting. Social contact often occurred during resting. Thus, the nest box and elevated location, in conjunction with social contact seem to be valuable while resting. While active, the foxes utilised the cage floor and roof of the nest box instead of the platforms. Scratching, digging and an interaction with the wooden block were seldom observed. Activity occurred mainly on the ‘empty’ cage area. In conclusion, all studied resources provided blue foxes with a distinct value, as they all were used in the complex housing environment. The nest box is used most and for most variable behaviours.     

Microclimate in two types of rat cages

The microclimate in two types of rat cages (a Makrolon type IV with a solid floor and a stainless steel cage with a wire mesh floor (five rats per cage)) placed in the same macro-environment was compared. The temperature, relative humidity and ammonia concentration in the cages were measured twice a day for 8 days. The cages were cleaned every 4 days. The greatest difference between the cage types was in the ammonia build-up. In Makrolon cages the ammonia concentration never reached 5 ppm, whereas in steel cages it showed a constant increase and already exceeded the threshold limit for man (25 ppm for 8 h per day) on the third day after cleaning.     

Blue foxes’ motivation to gain access to solid floors and the effect of the floor material on their behaviour

Farmed blue foxes are willing to work to gain access to a sand floor from a wire mesh floor. It is not clear whether the foxes work for the sand floor because of its solidity or because it enables them to perform certain behaviours, e.g. exploration and digging. Here, we measured blue foxes’ motivation to gain access from a wire mesh floor to a floor with 15–30 cm deep sand, a floor with 3–4 cm deep sand, a solid concrete floor, and another wire mesh floor. In addition, we analysed the foxes’ behaviour on these floor materials. Seven male blue foxes were trained and tested in self-constructed operant apparatuses. In an apparatus, the fox could move a bottomless test cage from a wire mesh floor to a neighbouring, alternative floor material for a 4-min visit by pressing a lever in the test cage for a fixed number of times (Fixed Ratio, FR). The foxes worked for each floor material for 12 days. In each daily test session, the foxes were exposed to work on one of the four workloads (FR 6, 12, 24, 48), for 3 h. The behaviour of the foxes was analysed during the 4-min visits on each floor material. The results showed that there was no difference between the floor materials, either in the demand elasticity of the fragment of the demand curve (ranging from −0.46 to −0.33), or in the intensity of the demand. However, the foxes’ behaviour varied between the floor materials. More digging, play, rooting (exploration with the muzzle), and vole jumping were observed on the floor materials with sand, than on the concrete floor and the wire mesh floor. Both the presence and the depth of the sand layer stimulated these behaviours. It is concluded that juvenile blue foxes do not value solid floor materials more than a wire mesh floor. However, the sand floor stimulates more digging, play, vole jumping, and exploration than the concrete floor or wire mesh floor. Furthermore, the depth of sand may be an important factor in eliciting these behaviours. Access to a floor material with sand may improve the welfare of farmed blue foxes by providing the possibility to perform species-specific behaviours.     

Effects of semi-group housing and floor type on pododermatitis,spinal deformation and bone quality in rabbit does

The most common housing system for reproduction rabbits, individual cage housing on a wire floor, is increasingly scrutinized because of its potential detrimental impact on animal welfare. We compared three types of housing: (1) individual cage housing on a wire floor (3952 cm²/doe, maximum roof height 63 cm, one 1000 cm² plastic footrest/doe), (2) semi-group housing on a wire floor (5000 cm²/doe, roofless, one 1000 cm² plastic footrest/doe) and (3) the same semi-group housing, but with a fully plastic slatted floor. In all housing systems, does had free access to an elevated platform. In the semi-group housing pens, four does were housed communally during 21 days of the reproduction cycle (to allow more space for locomotion and to increase opportunities for social contact), and individually during the other 21 days of the cycle (to minimize doe–doe and doe–kit aggression that peaks around kindling). In all, 24 Hycole does were included per system. The does entered the experiment at 203 days of age (after their first parity). The experiment consisted of four reproductive cycles, ending at 369 days of age. Pododermatitis was scored in cycles 1, 2 and 4. At the end of the 4^th cycle the does were euthanized and X-rays were taken to assess spinal deformation. Tibia and femur length, width and cortical thickness were determined and bone strength was assessed using a shear test, as a measure of bone quality. Although severe pododermatitis was absent, the prevalence of plantar hyperkeratosis (hair loss and callus formation) at the end of the 4^th cycle was much greater on the wire floor (65% and 68% for semi-group housing and individual cages, respectively) than on the plastic floor (5%, P<0.0001), even though the wire floors were equipped with a plastic footrest known to decrease hyperkeratosis. In contrast to our expectations, semi-group housing did not affect the prevalence of spinal deformations (P>0.10), but in line with our expectations bone quality was affected favourably by semi-group housing. The tibial cortex (and to a lesser extent the femoral cortex) was thicker in semi-group housing than in individual cages (1.45, 1.46 and 1.38 mm for semi-group housing on wire, semi-group housing on plastic and individual housing on wire, respectively, P=0.045). What this increase in cortical thickness means in terms of doe welfare requires further study, as it may reflect an increase in activity resulting either from increased space for locomotion, or from fleeing aggressive pen mates.     

Salmonella in Wastes Produced at Commercial Poultry Farms

Composite samples of freshly voided excreta from 91 poultry houses were tested qualitatively for Salmonella; 26 (29%) were positive. The houses were located on 36 farms, 18 of which (50%) yielded one or more positive samples. In a separate, quantitative study, Salmonella densities ranged from less than 1 to over 34,000 per g of excreta (dry weight). High densities were noted in waste from cage houses, but not in waste from floor houses (litter or wire floors). Salmonella-shedding chickens were located in only one small area of the row of cages examined in detail. A total of 15 Salmonella serotypes were identified during the study.     

笼底类型对肉仔鸡行为的影响及其与胸囊肿发生率的关系

为研究笼养肉仔鸡胸囊肿发生的行为学机制,观察比较3种盒式笼(笼底分别由铁丝网、塑料片和竹竿组成)中肉仔鸡从3至6周龄的行为,以及胸囊肿发生率的差异。结果表明6周龄时,肉仔鸡在3种笼底上的伏卧行为虽无显著差异,但在行为格局中其比例最高(均在70%以上),而站立、行走和晃动3种行为之和仅占10%左右;竹竿笼底上的肉仔鸡行走频次、晃动频次和比例均显著高于铁丝和塑料笼底上的(均P<0.05),而竹竿笼底上的肉仔鸡胸囊肿发生率显著低于铁丝笼底上的(P<0.05);随着周龄增长,铁丝笼中肉仔鸡行走和晃动频次均减少,伏卧时间延长,胸骨承受的重量增大,这增加了胸部与铁丝网笼底接触及摩擦的几率和时间。实验结果说明,笼养肉仔鸡行为格局趋向静态单一化(动态行为频次降低,静态行为比例占优势)与其胸囊肿发病率的变化相一致,提示两者存在某种内在联系。这验证了我们提出的假设,即依赖于笼底类型和周龄的肉仔鸡行为趋向静态性是胸囊肿形成的必经环节。     

The effects of different types of individually ventilated caging systems on growing male mice

Ventilation rate and turnover rate of dry air vary among different types of ventilation systems used with individually ventilated cages (IVCs) and can affect the well-being of rodents housed in these cages. The authors compared the effects of two types of IVC systems, forced-air IVCs and motor-free IVCs, on 4-week-old C57Bl/6J male mice. The mice were acclimatized to the cages for 8 d and then monitored for 87 d. Their body weights, food and water consumption and preferred resting areas were recorded. Mice that were housed in motor-free IVCs had a significantly greater increase in body weight than those housed in forced-air IVCs, despite having similar food consumption. Mice in forced-air IVCs had greater water consumption than mice in motor-free IVCs. In addition, mice in forced-air IVCs were more frequently located in the front halves of their cages, whereas mice in motor-free IVCs were located with similar frequency in the front and back halves of their cages, perhaps because of the higher ventilation rate or the location of the air inlets and outlets in the rear of the cage. These results suggest that body weight, food and water consumption and intracage location of growing male mice are influenced by the type of ventilation system used in the cages in which the mice are housed.     

Evaluating the impact of predation by fish on the assemblage structure of fishes associated with seagrass (Heterozostera tasmanica) (Martens ex Ascherson) den Hartog, and unvegetated sand habitats

The role of fish predation in structuring assemblages of fish over unvegetated sand and seagrass was examined using enclosure and exclusion cages to manipulate the abundance of predatory fish from November 1998 to January 1999. In our exclusion experiment, piscivorous fish were excluded from patches of unvegetated sand and seagrass to measure how they altered abundances of small fishes, i.e., fish <10 cm in length. Habitats from which piscivorous fish were excluded contained more small fish than those with partial cages, which in turn contained more fish than uncaged areas. These patterns were consistent between unvegetated sand and seagrass areas, although the relative differences between predator treatments varied with habitat. Overall, small fish were more abundant in unvegetated sand than seagrass. Atherinids and syngnathids were the numerically dominant families of small fish and varied in complex ways amongst habitats and cage treatments. The abundance of atherinids varied inconsistently between cage treatments through time. Only during the final two sampling times did the abundance of atherinids vary significantly across cage treatments. Syngnathids were strongly associated with seagrass and were significantly more abundant in caged than uncaged habitats. In our enclosure experiment, five individuals of a single species of transient piscivorous fish, Western Australian salmon (Arripidae: Arripis truttacea Cuvier), were enclosed in cages to provide an estimate of the potential for this species to impact on small fish. The abundance of small fish varied significantly between cage treatments. Small fish were more abundant in enclosure cages and exclusion cages than uncaged areas; however, there was no difference in the abundance of small fish in enclosure cages and partial cages, and no difference between exclusion cages and partial cages. These patterns were consistent amongst habitats. Atherinids and syngnathids were again the numerically dominant families of small fish; atherinids varied more with cage structure while syngnathids did not vary statistically between cages, blocks (locations within which a single replicate of each cage treatment was applied) or habitats. Dietary analysis of caged A. truttacea demonstrated the potential for this species to influence the assemblage structure of small fish through predation - atherinids were consumed more frequently in unvegetated sand than seagrass, and syngnathids were consumed only in seagrass, where they are most abundant. Observations of significant cage or predation effects depended strongly on the time at which sampling was undertaken. In the case of the atherinids, no predation or cage effects were observed during the first two sampling times, but cage effects and predation effects strongly influenced abundances of fish during the third and fourth sampling times, respectively. Our study suggests that transient piscivorous fish may be important in structuring assemblages of small fish in seagrass and unvegetated sand, and seagrass beds may provide a refuge to fishes. But the importance of habitat complexity and predation, in relation to the potentially confounding effects of cage structure, depends strongly on the time at which treatments are sampled, and the periodicity and multiplicity of sampling should be considered in future predation studies.     

Response of grazing impacts of an algivorous fish (Pseudogastromyzon myersi: Balitoridae) to seasonal disturbance in Hong Kong streams

1. Manipulative experiments were carried out in four Hong Kong streams (two shaded, two unshaded) to investigate the impact of grazing by an algivorous fish, Pseudogastromyzon myersi, on benthic algal biomass and assemblage composition. Experiments were conducted and repeated during both the dry and wet seasons to determine whether spate‐induced disturbance modified any grazing effect. Treatments comprised fish exclusion and inclusion via closed and open cages, with a no‐cage treatment used as a control for the cage effect. Treatments were maintained for 4 weeks in each experimental run. 2. Grazing by P. myersi reduced benthic algal biomass and the organic matter content of periphyton in open cages and the no‐cage treatment relative to closed cages. The similarity between open‐cage and no‐cage treatments was evidence that the overall difference among treatments was caused by limiting fish access to closed cages and not merely an artifact of caging. Grazing effects were broadly similar in all streams, but there was a significant statistical interaction between treatments and seasons. 3. Analysis of dry‐season data matched the overall trend in inter‐treatment differences, confirming the effects of grazing by P. myersi on algal biomass and periphyton organic matter. Significant differences in algal assemblage composition between closed‐cage and no‐cage treatments during the dry season reflected reductions in the abundance of erect, stalked diatoms (Gomphonema) and filamentous cyanobacteria (Homeothrix). Removal of these vulnerable overstorey algae by P. myersi resulted in greater abundance of understorey diatoms (Achnanthes and Cocconeis) in the no‐cage treatment in all streams during the dry season. The composition of algal assemblages in open cages was intermediate between the other two treatments. 4. Although fish densities were greater in all streams during the wet season, spate‐induced disturbance obscured grazing effects and there were no significant differences among treatments attributable to fish grazing. Seasonal variation in impacts of P. myersi grazing provides support for the harsh‐benign hypothesis, and confirms that biotic factors are less important controls of stream algal biomass and assemblage structure during periods (i.e. the wet season in Hong Kong) when abiotic disturbances are frequent or intense.     

Effects of cage density on behavior in young adult mice

Optimal housing conditions for mice can be achieved by minimizing environmental variables, such as those that may contribute to anxiety-like behavior. This study evaluated the effects of cage size on juvenile mice through assessment of differences in weaning weight, locomotor skills, and anxiety-like behavior. Eighteen pairs of male and pregnant female Swiss-Webster (Cr:SW) mice were housed in 3 different caging scenarios, providing 429, 505, or 729 cm2 of space. Litters were standardized to 10 pups per litter in each cage. Mice reared in each caging scenario were assessed with the open-field, light-dark exploration, and elevated plus-maze tests. No differences in weaning weight were noted. Mice reared in the 505- and 729-cm2 cages explored a significantly larger area of the open-field arena than did those in the 429-cm2 cages. Those reared in the 505-cm2 cages spent more time in the center of the open field than did those in the 729-cm2 cages, suggesting that anxiety-like behavior may be increased in the animals housed in the larger cages. This study did not establish a consistent link between decreased floor space and increased anxiety-like behavior; neither does there appear to be a consistent effect of available floor area on the development of locomotor skills on mouse pups.     

Cage-change interval preference in mice

Before animal research facilities began using individually ventilated cage (IVC) systems for mice, cages were often changed one or more times per week. When using IVC systems, however, it is standard practice to change cages only once every 2-3 weeks. When deciding how often to change cages, personnel may consider the cost of labor needed to change the cage, as well as the cage type and bedding type, rather than animal preference or concern for animal well-being. The authors carried out a simple preference test in groups of mice. Mice were allowed to choose between an unsoiled cage and cages that had not been changed for 1 d, 7 d or 14 d. When evaluating where mice positioned their nests and the amount of time mice spent in the various cages, the authors found that the mice preferred the unsoiled cage. Younger mice (<150 d old) showed a stronger preference for the unsoiled cage than did older mice (>150 d old). Further studies are warranted to evaluate mice's preferences for cages changed at different intervals and to determine whether prolonging the interval between cage changes has any negative effects on mice.     

Affiliation and social discrimination produced by brief exposure in day-old domestic chicks.

Discrimination between individual strangers and companions was examined in day-old domestic chicks. In one experiment, pecking rates at companions and strangers were observed in pairwise bouts after 16 hr of cohabitation. The discriminability of strangers and companions was varied by means of pre-hatch colouring. Reliable discriminations between individual strangers and companions emerged as early as the first minute of the encounter. Discriminative cues provided by artificial colouring were found not to be necessary in establishing social discrimination. In a second experiment, undyed chicks were housed in pairs for 1, 4 or 16 hr. Half of the pairs lived in cages that separated companions by a wire screen, and half were housed in undivided cages. Observations of pecking in four-way bouts confirmed previous findings and demonstrated that the opportunity to peck during exposure may be a necessary condition in producing social discrimination. Antecedent conditions that lead to the development of affiliative bonds simultaneously appear to establish social discrimination.     

Floor- and cage-rearing effects on pullets'' initial adaptation to multiple-hen cages

White Leghorn pullets reared in floor pens and high-density cages were compared for behavioral traits and changes in body weights during the initial 2 or 3 weeks after being placed in multiplehen cages during late adolescence. Information on behavior was obtained from 48 pullets kept in 6, 8-bird cages during Days 1, 4 and 15 in Experiment 1, and from 80 pullets kept in 16, 5-bird cages during Days 1 and 7 or 8 in Experiment 2.

In Experiment 1, floor-reared pullets showed significantly more crouching, less movement and lower feed consumption than cage-reared pullets during Day 1. By Day 4, floor-reared pullets still consumed significantly less feed, but by Day 15, no differences were found for crouching, movement or feed eaten. Cage-reared pullets had more feather-pecking on Day 1 but less on Day 15 than floor-reared ones. Pullets from the two rearing environments did not differ in post-housing daily gain in body weight.

In Experiment 2, floor-reared pullets had significantly fewer feeding bouts during Day 1, but they did not differ from cage-reared pullets during Days 7 or 8. Although pullets from floor-pens fed significantly less frequently, they had longer durations of feeding bouts, so that total time feeding did not differ from that of cage-reared pullets. Diurnal feeding patterns changed significantly from Day 1 to Day 7 or 8. Correlation coefficients between measures of individual pullet's feeding behavior and body weight at housing did not differ significantly from zero. Duration of individuals' feeding bouts on Day 7 or 8 was moderately and significantly correlated with their body-weight gain for the first 21 days after housing. Gains in body weight did not differ for pullets from the two rearing treatments.

Most aggressive acts occurred just inside the front of the cages, adjacent to the feed trough; few were seen directly over the feed. Agonistic activity and percentage of dominance relationships known were greater among floor-reared than among cage-reared pullets after transfer to laying-house cages. Decreases in frequency of aggressive acts occurred from Day 1 to Day 7 or 8 for pullets from both rearing environments.     

Transient hypertension and sustained tachycardia in mice housed individually in metabolism cages

The novel environment of a metabolic cage can be stressful for rodents, but few studies have attempted to quantify this stress-response. Therefore, we determined the effects on mean arterial pressure (MAP) and heart rate (HR), of placing mice of both sexes in metabolism cages for 2 days. After surgical implantation of a carotid artery catheter mice recovered individually in standard cages for 5 days. Mice then spent 2 days in metabolism cages. MAP and HR were monitored in the standard cage on Day 5 and in metabolism cages on Days 6-7. MAP increased by 18+/-3 and 22+/-4 %, while HR increased by 27+/-4 and 27+/-6 %, in males and females, respectively, during the first hours after cage switch. MAP decreased to baseline in the fourth and eighth h following metabolism cage switch in males and females, respectively. However, HR remained significantly elevated in both sexes during the entire two-day period in metabolism cages. Females had lower MAP than males both pre- and post-metabolism cage switch, but there were no sex differences in HR. These results demonstrate sustained changes in cardiovascular function when mice are housed in metabolism cages, which could potentially affect renal function.     

Design and construction of cage environments for air ion and electric field research

This report describes the design and construction of cage environments suitable for chronic exposures of large groups of mice to air ions and electric fields. These environments provide defined and reproducible ion densities, ion flux, DC electric fields, sound levels, air temperature and air quality. When used during a 2 year study, these cage environments served as a durable and reliable continuous exposure system. Three environmental chambers (cubicles) housed a total of 12 cages and provided control of air temperature, air purity and lighting. Exposure cages had grounded metal exterior walls, a plexiglass door and interior walls lined with formica. An internal isolated field plate supplemented with guard wires, energized with ca 1000 VDC, created about a 2 kV/m electric field at the grounded cage floor. Air ions resulted from the beta emission of sealed tritium foils mounted on the field plate. Cages provided high ion (1.3×10⁵ ions/cc), low ion (1.6×10³ ions/cc) and field only (ion depleted < 50 ions/cc) conditions for both polarities with similar electric fields in ionized and field only cages. Detailed mapping of the floor level ion flux using 100 cm² flat probes gave average fluxes of 880 fA cm^–2 in high ion cages and 10 fA cm^–2 in low ion cages. Whole body currents measured using live anesthethized mice in high ion cages averaged 104±63 pA. Both ion flux and whole body currents remained constant over time, indicating no charge accumulation on body fur or cage wall surfaces in this exposure system.     

Assessment of preference for grid-flooring and sawdust-flooring by captive-bred marmosets in free-standing cages

Marmosets (Callithrix jacchus) in a captive breeding colony living in metal caging, with wooden shelves and perches, were assessed by video recording for the time spent on the floor of the cage when that floor was a wire grid above a sawdust-filled tray and when it had been changed to a sawdust-filled tray several days previously. Quantitative analysis of these videos indicated that marmosets made more visits to the floor when it comprised a wire grid than when it comprised a sawdust-filled tray. They also tended to spend more time on the floor when the floor was a wire grid. These results suggest that this arboreal species does not necessarily share the need or preference for contact with a particle-covered solid floor which might be considered appropriate for a terrestrial species.     

Aspen wood-wool is preferred as a resting place, but does not affect intracage fighting of male BALB/c and C57BL/6J mice

Aspen wood-wool, provided as nesting material, was evaluated as a possible improvement of cage environment for 10-14-week-old inbred male mice maintained in groups of six (BALB/c n = 72 and C57BL/6J n = 36). The daily behaviour of mice was video recorded and their body weight, food consumption, weights of some organs and serum corticosterone concentrations were measured. Aggressive interactions between cage mates and against a strange intruder as well as the number of wounds on the back of the animals was monitored in order to evaluate the effect of nesting material on intermale aggression. Nesting material did not affect the daily active/passive behaviour patterns of mice, although animals clearly preferred it as a resting place. BALB/c mice given nesting material showed less weight gain and smaller brown adipose tissue weights than animals without nesting material. The other characteristics measured were not affected by the presence of nesting material in either strain. The presence of nesting material had no effect on fighting in cages. C57BL/6J mice were more aggressive than BALB/c mice according to the number of wounded animals in a cage. Wounded BALB/c mice had enlarged spleens and decreased epididymal adipose tissue weights. In conclusion, the nesting material used in this study did not adversely affect the animals. On the other hand, the material was clearly preferred to conventional bedding as a resting place. These findings suggest that nesting material may improve the cage environment of laboratory mice. Furthermore, there was an indication of strain differences in aggressive behaviour. It could be suggested that C57BL/6J mice are less tolerant towards intruders and housing six mice per cage is not suitable for this strain.