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.     

Comparative nutrient digestibility of arctic foxes (Alopex lagopus) on Svalbard and farm-raised blue foxes (Alopex lagopus)

Arctic foxes from Svalbard (n=4) and farmed blue foxes (n=4) was used in a digestibility experiment with a high-carbohydrate feed to add more information to the nutritional physiology of the arctic fox, and to compare its digestive capacity with that of the farmed blue fox. The arctic fox has a diet containing mainly protein and fat from mammals and birds, while farmed blue foxes have been exposed to an omnivorous dietary regime for more than 80 generations. The experiment showed in general no difference in digestive capacity for protein and fat between the foxes (P>0.05), but for carbohydrates, including starch and glucose, the blue fox revealed higher digestibility values. The superior digestive capacity for carbohydrates in blue fox might be a result of a long-term selection of animals digesting dietary carbohydrates more efficiently, or that an early age exposition to dietary carbohydrates has given permanent improvement of the carbohydrate digestion in the gut.     

Reproductive management of silver foxes (Vulpes vulpes) in captivity

Specific protocols need to be developed that take into consideration the requirements of silver foxes. This study was designed to investigate the reproduction of 26 pairs of silver foxes (Vulpes vulpes). Reproduction parameters (breeding season, age at puberty, fecundity and fertility) of the foxes were examined under experimental conditions, and new techniques to optimize fox breeding were assessed. Staining of the vaginal smears with the double Harris-Schorr stain allowed for the precise detection of estrus and proved to be more reliable than simply measuring vaginal resistance. Ultrasonography was demonstrated to be useful for pregnancy diagnosis and prediction of parturition. Results demonstrate that the methods reported in this paper are easily applicable to similar studies carried out on small groups of animals within the framework of fox animal experimentation.     

Nest box orientation affects internal temperature and nest site selection by Tree Swallows

ABSTRACT.   Orientation of nests can influence nest microclimate, particularly temperature. However, few investigators have examined orientation preference and microclimate simultaneously. We examined the possible correlation between entrance orientation of artificial nest boxes used by Tree Swallows ( Tachycineta bicolor ) and the internal temperature of boxes. Tree Swallows showed a preference for east- and south-facing boxes, but only during the first half of the breeding season (before 1 June). During the second half of the breeding season (after 1 June), Swallows selected boxes based on availability. We found that east- and south-facing boxes were warmer than north- and west-facing boxes, but only during the first half of the breeding season when those boxes were preferred. Entrance orientation and box temperature were only correlated during the morning (06:00–12:00); the temperature of all boxes was similar during the afternoon. Our results suggest that Tree Swallows show a preference for nest boxes with a certain entrance orientation only when orientation influences microclimate, suggesting that warmer nest temperatures may provide fitness benefits.     

Comparative aspects of sperm membrane fatty acid composition in silver (Vulpes vulpes) and blue (Alopex lagopus) foxes, and their relationship to cell cryopreservation

Cryogenic protocols have been developed for the storage of farmed silver fox (Vulpes vulpes) spermatozoa. However, these same protocols and modifications of these protocols have failed to satisfactorily preserve spermatozoa collected from farmed blue foxes (Alopex lagopus). Because cryogenic success has been linked to membrane composition, the plasma membrane lipid composition of farmed blue fox and silver fox spermatozoa was studied. Silver fox spermatozoal membranes have significantly higher levels of docosapentaenoic acid (DPA; 22:5, n-6) compared to blue fox spermatozoa, and blue fox spermatozoal membranes have significantly higher levels of stearic acid (18:0). Silver fox spermatozoal membranes not only have a higher ratio of unsaturated/saturated membrane fatty acids, but also higher levels of membrane desmosterol and cholesterol.     

Milk intake in blue fox (Alopex lagopus) and silver fox (Vulpes vulpes) cubs in the early suckling period

Milk intake of fox cubs (2-16 days of age; body weight, 96-649 g) in ten blue fox litters and ten silver fox litters were measured by the water isotope dilution (WID) technique following a single intraperitoneal injection of tritiated water (3HHO). Litter size varied from four to 14 in blue foxes and from three to eight in silver foxes. Silver fox cubs had higher birth weights than blue foxes. Inter-species body weights and growth rates were apparently dependent on litter size and the dam's constitution. In both species growth rate increased with age and body weight (7-35 g per day). In the cubs, the biological half-life of body water turnover (BWT) rose from 1.5 days at 2-3 days of age to 2.5 days at 13-16 days of age, although a considerable scatter was seen. The mean daily milk intake of the cubs varied with body weight, from 31 to 193 g per day, whereas daily milk intake per unit of body mass remained stable at 30-35 g per 100 g body weight. The ratio of milk intake to body weight gain varied considerably among cubs, averaging 4.5 g/g during the 3-week experimental period. In suckling fox cubs, the calculated daily intake of metabolically energy (ME) corresponded fairly with the estimated energy requirements for growth and maintenance of the young. Finally, the applicability and the accuracy of the WID technique was evaluated in ten 3-week-old fox cubs, by tube-feeding with a milk replacer for 48 h, which documented that the daily rates of milk intake and water turnover can be accurately measured in suckling fox cubs by the WID technique following a single injection of 3HHO.     

Selection of nest sites by a hole-nesting duck, the Goldeneye Bucephala clangula

Nest site preferences were examined for a population of Goldeneye Ducks breeding in nest boxes in Värmland, central Sweden. Some nest boxes were occupied more often than others even if females returning to the same nest box were excluded from the analysis. Nest boxes located higher up trees were occupied more often than those close to the ground and some spatial 'cluster groups' of boxes were occupied more often than others. Otherwise nest site prefernces were not related to any measured physical attributes of the boxes. Prefernces for nest boxes seemed to be based mainly on a tendency for females to select those that had been occupied by other females in the preceding year, especially if they had bred successfully. As a result of this, the occupancy of nest boxes was not random over years but rather progressed in a series of runs; a period of consecutive years in which a box was occupied was followed by a period of years in which it was empty.
There were reproductive consequences for these prefernces in that females occupying preferred boxes were less likely to lose their clutch to a predator. These females also bred earlier in the year and produced larger clutches and broods than females breeding in other boxes.     

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.     

Genetic polymorphism of plasma α1B-glycoprotein and transferrin in arctic and silver foxes

Plasma samples of 235 foxes from 38 complete families (14 of arctic foxes, 21 of silver foxes and 3 with arctic x silver fox hybrid offspring) were analysed by one-dimensional horizontal polyacrylamide gel electrophoresis (PAGE) pH 9.0 followed by general-protein staining of gels. A major postalbumin of fox plasma was identified as alpha 1B-glycoprotein (alpha 1B) by using immunoblotting with antiser m specific to human or pig plasma alpha 1B. Four codominant, autosomal alleles of alpha 1B were found in arctic foxes. Two transferrin (TF) alleles (TfF, TfS) were observed in arctic foxes and two (TfD, Tff) in silver foxes; the TF F type of both of the fox species showed identical electrophoretic mobilities. The arctic foxes showed a high degree of polymorphism for both TF and alpha 1B. The silver foxes showed a scarce polymorphism of TF and were monomorphic for alpha 1B. The arctic fox, silver fox and their hybrids could be clearly differentiated from one another by their plasma protein patterns obtained by the PAGE method.     

Parent birds assess nest predation risk: influence of cavity condition and avian nest predator activity

Skutch hypothesized that nest predators visually assess parental activities to locate a prey nest, whereas parents modify fitness‐related traits to reduce the probability of nest predation. We examined how cavity condition and parental activity interact with avian nest predators to shape the nest success of two coexisting parid species, marsh tits Poecile palustris and oriental tits Parus minor, breeding in nest‐boxes during the incubation period. Nest‐boxes were manipulated to create a prolonged risk of nest predation (entrance diameter 2.6 cm control vs 5.5 cm treatment) soon after clutch completion. To measure changes in parental behavior, we also simultaneously simulated a pulsed risk of nest predation, using sound playbacks of a coexisting control bird and an avian nest predator. We found that the parent tits merely responded the pulsed risk, presumably due to an environment with high avian nest predator encounters, compared to the prolonged risk. Instead, both species spent more time on vigilance at the nest, only under prolonged risk conditions. The activity of corvids near the nest‐box was higher in the marsh tit than that in oriental tits. This activity was also higher in the treatment nest box than that in the control nest‐box. Nest predation during the incubation period was higher in marsh tits than in oriental tits, presumably due to higher and more plastic vigilance in oriental tits, compared to marsh tits. Our results highlight that the differences in cavity condition and parental activities at the nests of two coexisting non‐excavators may contribute to differential nest predation by attracting avian nest predators.     

Specific nest box designs can improve habitat restoration for cavity‐dependent arboreal mammals

Tree‐cavity‐dependent wildlife faces future shortages of cavities due to a decline in the abundance of large, old trees in many parts of the world. Nest boxes are proposed as a tool to restore habitat value but evidence of their effectiveness for arboreal mammals remains equivocal. This may arise from a poor understanding of design preferences. We conducted investigations in two landscapes in eastern Australia to determine whether species show a preference for specific designs. We observed a preference by some mammal species for particular designs (33–78% occupied/used), suggesting that design refinement can improve the frequency with which nest boxes are used. Although feral species may out‐compete target species for nest boxes, we did not observe this. We recorded feral honeybees (Apis mellifera) in 6–9% of nest boxes but they did not remain, and many occupied boxes were later used by mammals. The introduced common myna bird (Acridotheres tristis) was prevalent in one landscape, but competition for nest boxes was localized. For nest boxes to be an effective habitat restoration tool, they must be able to be occupied over long periods of time. We investigated this for the squirrel glider (Petaurus norfolcensis), an arboreal marsupial threatened through part of its geographic range. Squirrel gliders occupied and bred within nest boxes (100% used) at two locations continuously over a 10‐year period with minimal nest box maintenance. Individuals occupied boxes for up to 7 years. This confirms that targeted nest box programs can be an effective restoration tool for cavity‐dependent arboreal mammals.     

Immigration stabilizes a population of threatened cavity‐nesting raptors despite possibility of nest box imprinting

Nest box provisioning is a common management tool intended to increase population size or stability of threatened birds, but its effectiveness is rarely assessed. The provisioning of nest boxes may lead to unexpected results if nest type imprinting prevents naïve adult birds from immigrating into the nest box population, or limiting the ability of juveniles reared in nest boxes to emigrate to areas with only natural nesting substrates. We analyzed the population trends from 2008 to 2010 of southeastern American kestrels Falco sparverius paulus associated with a network of nest boxes in north‐central Florida, USA, with Bayesian integrated population models (IPMs) that simultaneously considered mark–recapture data sets, fledgling production, and population surveys. We evaluated the demography of the nest box population by comparing population growth rates, apparent survival probabilities, and recapture probabilities between an IPM that explicitly modeled immigration and one that did not. Overall population growth rates suggested that the population was stable, and that immigration was apparently important in maintaining this stability, with approximately 0.3 and 0.5 female immigrants per resident female kestrel each year. Explicitly modeling immigration resulted in lower estimates of juvenile kestrel apparent survival probability, suggesting that a large proportion of locally produced juveniles emigrated rather than recruited locally. We concluded that neither preference for natural cavities nor imprinting on artificial nest boxes appeared to prevent immigration from maintaining the stability of the local population. Natal habitat preference imprinting on nest sites may occur to some degree, but it did not preclude the adoption of nest boxes by most breeding kestrels. We also found additional indications that many juvenile kestrels fledged from nest boxes emigrated to the surrounding natural areas.     

Inter- and intraspecific competition between the fox species Alopex lagopus and Vulpes vulpes: an evaluation trial under penned conditions

This study compared competition capacity and dominance relations between arctic foxes (Alopex lagopus) and red foxes (Vulpes vulpes). Experiments were carried out in semi-natural earthen floor enclosures using farm-bred colour types of both species (blue fox and silver fox) as subjects. Results of the dominance scoring and open field behaviour after weaning in August-September showed that blue foxes dominated over silver foxes. Thereafter, the situation gradually became reversed and silver foxes were dominant during the breeding and whelping seasons. Housing both species together from weaning produced more curious animals as compared to when these species were placed in common quarters after the autumn equinox. In the case of blue foxes, the male dominated highly over all females. In silver foxes, the difference in dominance between the sexes was, however, less pronounced. The most dominant individuals in the study groups were typically among the heaviest. Breedings and whelpings succeeded better in silver than in blue foxes. However, none of litters born survived more than one week. The present results support the conclusion that when both fox species are housed together, Vulpus vulpus tends to dominate over Alopex lagopus. Received: 22 March 1996/Accepted: 30 June 1996     

Diet of arctic foxes (Alopex lagopus) in Iceland

Arctic foxes, Alopex lagopus , live in low productivity arctic and northern tundra habitats, where they generally prey heavily on lemmings. In Iceland, however, no lemmings are present, and the foxes have a very varied diet, including plants such as seaweed and black crowberries, a wide range of birds and invertebrates, and carcasses of large mammals such as seals, reindeer, and sheep. Marked seasonal, geographical and inter-annual differences confirm arctic foxes in Iceland as opportunistic feeders. There are coastal and inland foxes: coastal foxes feed mainly on prey derived directly or indirectly from the ocean, particularly various seabirds and seals, while inland foxes feed largely on migrant birds, such as geese, waders and passerines in summer, and ptarmigan in winter. Despite their reputation for killing lambs, in this study, lamb carcasses were found at only 19.4% of 1125 fox dens, 44% of which had only one carcass. The distance to the nearest farm and the physical condition of lambs were major determinants of the number of carcasses found at a den. We discuss the implications of arctic foxes' diet for population dynamics and group formation, and for management practices.     

Do nest boxes in restored woodlands promote the conservation of hollow‐dependent fauna?

Vegetation restoration is considered as an important strategy for reversing biodiversity decline in agricultural areas. However, revegetated areas often lack key vegetation attributes like large old hollow‐bearing trees. As these trees take a long time to develop, artificial cavities such as nest boxes are sometimes provided to address lag effects. We conducted a 3‐year experiment using 150 nest boxes with 4 designs to quantify patterns of occupancy within 16 replanted areas and 14 patches of remnant old‐growth eucalypt woodland. We quantified patterns of occupancy of nest boxes in physically connected versus isolated remnants and plantings, and multiple covariate effects on nest box occupancy at the nest box, tree, patch, and landscape levels. Our analyses revealed a lower probability of nest box occupancy within remnants (vs. plantings) for 2 of the 6 response variables examined: any species and the Feral Honeybee. Nest boxes in connected remnants and plantings were more likely to be occupied than those in isolated plantings and remnants by any mammal and the Common Brushtail Possum. Nest boxes in restored woodlands are used by some hollow‐dependent fauna but principally already common species and not taxa of conservation concern. Nest boxes were also used by pest species. A key management consideration must be to create connected habitat to facilitate colonization of nest boxes by mammals. Approximately 15% of the cavity‐dependent vertebrates within the study area used next boxes, possibly because the diverse requirements of the array of other species were not met by the range of nest boxes deployed.     

Does nest box use reduce the fitness of a tree-cavity dependent mammal?

Nest boxes are frequently used in conservation programs for tree-cavity dependent wildlife. There is growing concern that the poor insulation properties of nest boxes may produce an ecological trap, because species may require microclimates less extreme or less variable than those experienced inside nest boxes. I investigated the fitness consequences of nest box use in a non-flying mammal. Fifty-two of 104 squirrel gliders (Petaurus norfolcensis) trapped over a 3-year period used nest boxes. Population modelling of the capture data revealed that the probability of apparent survival increased with increasing nest box use. There was no difference in breeding frequency between females that used or did not use nest boxes. There was no evidence that offspring development was hindered within nest boxes. These findings may arise because: (1) gliders could access tree hollows during extreme temperatures, (2) ambient temperatures were mild during the study, (3) gliders construct leaf nests which insulate against low temperatures in winter, and (4) gliders breed between autumn and spring when temperatures are relatively benign. The estimate of annual survival of animals using nest boxes (0.60), was equivalent to estimates at locations where squirrel gliders were either reliant on nest boxes (0.54) or on tree cavities (0.55) for shelter. Studies such as this need to be conducted on a range of species across a range of locations to better understand the influence of nest box use on non-flying mammals.     

Effects of the risk of competition and predation on large secondary cavity breeders

The effects of competition and risk of predation on secondary cavity breeders were examined between the 2008 and 2009 breeding seasons using an experimental design manipulating two nest entrance sizes (large entrances allowed Barn Owls (Tyto alba) to enter, while the small entrances excluded them). During the 2009 breeding season, the entrance sizes of nest boxes were exchanged, so that if during one year a nest box in a particular location had a small entrance, the second year it had a large entrance and vice versa. Barn Owls and Eurasian Kestrels (Falco tinnunculus) occupied 67.3 and 17.3%, respectively, of large entrance nest boxes. Significantly more Jackdaws (Corvus monedula), House Sparrows (Passer domesticus) and Scops Owls (Otus scops) bred in nest boxes with small than with large entrances. After nest box entrance sizes were exchanged, Barn Owls and smaller species did not breed in the same nest boxes with the new entrance size. Jackdaws probably did not breed in large entrance nest boxes due both to exploitation competition (Barn Owls and Eurasian Kestrels occupied the majority of large entrance nest boxes), and may also have avoided empty nest boxes because of the risk of interference competition; whereas smaller species may have also avoided large entrance nest boxes due to risk of predation.     

Nest preference of laying hens (Gallus gallus domesticus) and their motivation to exert themselves to gain nest access

In connection with the development of a test method for the attractiveness and appropriateness of nests for laying hens, we carried out an investigation by using a preference test and motivation measuring with the help of push doors. Hens were offered two different nest sites either consisting of a tray filled with wood shavings (litter tray) or a wooden nest box plus wood shavings (nest box). Hens were individually housed in pens (2.0 m × 2.0 m) and had free access to the nest sites until they laid their 15th egg. From that day the hens had to overcome a push door to reach the nest sites. Resistance for entrance was also increased stepwise at the door leading to the hens’ nest. The experiment ended when a hen stopped to lay in her usual nest site for four consecutive days (postexperimental period). The behaviour during the last hour before oviposition was video taped at a level of resistance of 3.5, 6.0, 7.5 and 10.0 N.The hens were categorized into nest and litter layers depending on nest choice. All but one hen pushed maximum resistances between 11.5 and 18.0 N with no differences between nest and litter layers. Behaviour did not significantly change with increasing levels of resistance, but there were significant differences between nest and litter layers. Nest layers spent more time nesting than litter layers while the latter showed a strong tendency to more exploring behaviour. For litter layers, more entries through the push door leading to their nest site and more unsuccessful pushes were detected than for nest layers. According to our results, two types of layers could be distinguished whereas the two were equally motivated to access their nest site.     

Light affects parental provisioning behaviour in a cavity‐nesting Passerine

Nocturnal bird species possess special adaptations to maximise visual efficiency under low light levels. However, some typically diurnal species also experience low‐light environments. For example, cavity‐nesting Passerines raise broods in dark cavities and search for food in light‐abundant surroundings. It is not clear whether they possess special adaptations for low light vision or breed in cavities at the expense of impaired parental care. In this study, we tested whether light conditions affect the provisioning efficiency of great tits. We experimentally tested how the level of natural and artificially increased illumination inside nest boxes affects parental feeding duration, frequency and timing. We monitored 15‐h of provisioning activity of great tit parents when nestlings were day seven post hatch. We used traditional ‘dark’ nest boxes and ‘bright’ nest boxes with increased illumination obtained by using semi‐transparent plastic windows. The duration of single feedings were, on average, shorter in brightened nest boxes compared to dark ones. This difference tended to be higher early in the morning and in the evening, when the illumination in dark nest boxes was the lowest. Nest box type, however, did not influence feeding frequency or times of the onset and the end of feeding. Our findings provide new evidence for impaired efficiency of parental care due to lowered light conditions. Further research is needed to test whether prolonged feeding duration has negative effects on adult time budgets and nestling energy expenditures.