Temporal and geographical variation in skull size of the red fox (Vulpes vulpes) and the Eurasian badger (Meles meles) in Austria

Using museum material, we studied temporal changes in skull size of 185 red foxes (Vulpes vulpes Linnaeus, 1758) and 71 Eurasian badgers (Meles meles Linnaeus, 1758) collected in Austria between 1866 and 2007. Four measurements were taken and combined into principal components by means of a principal components analysis. Akaike's information criterion models indicated that skull size of the red fox and the Eurasian badger is positively related to the year of collection and negatively to altitude but not to latitude or longitude. However, for the Eurasian badger, the relationship between skull size and year is only on the verge of significance. We suggest that the increase in skull size with year is a result of improved food availability during the 20th Century from man‐made resources such as agricultural produce and garbage, and the decrease in skull size with altitude is possibly the result of a parallel decrease in primary productivity. © 2012 The Linnean Society of London, Biological Journal of the Linnean Society, 2012, ●● , ●●–●●.     

Mating system of the Eurasian badger, Meles meles, in a high density population

Badgers are facultatively social, forming large groups at high density. Group-living appears to have high reproductive costs for females, and may lead to increased levels of inbreeding. The extent of female competition for reproduction has been estimated from field data, but knowledge of male reproductive success and the extent of extra-group paternity remains limited. Combining field data with genetic data (16 microsatellite loci), we studied the mating system of 10 badger social groups across 14 years in a high-density population. From 923 badgers, including 425 cubs, we were able to assign maternity to 307 cubs, with both parents assigned to 199 cubs (47%) with 80% confidence, and 14% with 95% confidence. Age had a significant effect on the probability of reproduction, seemingly as a result of a deficit of individuals aged two years and greater than eight years attaining parentage. We estimate that approximately 30% of the female population successfully reproduced in any given year, with a similar proportion of the male population gaining paternity across the same area. While it was known there was a cost to female reproduction in high density populations, it appears that males suffer similar, but not greater, costs. Roughly half of assigned paternity was attributed to extra-group males, the majority of which were from neighbouring social groups. Few successful matings occurred between individuals born in the same social group (22%). The high rate of extra-group mating, previously unquantified, may help reduce inbreeding, potentially making philopatry a less costly strategy.     

Factors affecting population density, group size and territory size of the European badger, Meles meles

This paper discusses the relationship between the distribution and biomass of the main prey of European badgers, Meles meles and the badgers group size, territory size and population density. The distribution of areas rich in earthworms, Lumbricus spp., is correlated with badger range size, whilst badger group size increases with the biomass of worms per badger territory and badger density increases with overall worm biomass. Regulation of badger density in an area is likely to take place through regulation of group size, in the absence of other factors such as persecution and lack of suitable sett-sites.     

Sexual maturity and breeding season of the badger, Meles meles in Sweden

The paper describes the seasonal sexual activity of badgers collected in central Sweden. Ovulation- and pregnancy rates were determined for females in different age classes and males were examined for testis weight and occurrence of spermatozoa.     

Distribution, habitat utilization and age structure of a suburban fox (Vulpes vulpes) population

The occurrence of wild foxes in suburbia is discussed. It is shown that in London breeding populations of foxes are found 5 km from the city centre, and in the last 3 years foxes have been recorded in the very centre of the city. The fox population in London is shown to be heavily dependent on residential habitats for both daytime harbourage and when selecting sites for natal earths. The fox population is unevenly distributed in London, with a marked clumping of the adult population during most of the year. The age structure of the population is presented, and these data are compared with data for other canid populations. Conclusions are drawn as to the effects of conventional control techniques on the age structure of a fox population.     

Social organization and movement influence the incidence of bovine tuberculosis in an undisturbed high-density badger Meles meles population

1. The culling of European badgers Meles meles has been a central part of attempts to control bovine tuberculosis (TB) in British cattle for many years. Recent results, however, indicate that this approach could in practice enhance disease spread. 2. This paper looks at the relationship between TB incidence and badger ecology in a high-density population in south-west England, which has been the subject of a long-term intensive study. The principal aims were to relate the probability of TB incidence, as detected by culture of clinical samples (i.e. excretion of bacilli), at the level of the individual and of the social group to demographic processes, movement, social organization and disease dynamics. 3. The probability of an individual being an incident case was greater in groups where TB was already present, although this was less influential in groups that were subject to some instability in numbers. Both individuals and groups were more likely to be incident cases where the social group was diminishing in size, although no relationship was observed with group size itself. This suggests that the process of group size reduction rather than group size per se has most influence on disease dynamics. The likelihood that either an individual or a group was an incident case was positively correlated with both individual and group-level movement. When the proportion of females in a social group was high, the positive association between movement and incidence was found to be more pronounced and there was a significantly higher probability of incident cases among males. 4. These relationships highlight the importance of social structure in driving TB transmission dynamics in this stable, high-density badger population. The results support the idea that a stable social structure mitigates against new incident cases of disease, and are consistent with the contention that badger culling may create the social circumstances for enhanced transmission of TB.     

Genetic structure within and among regional populations of the Eurasian badger (Meles meles) from Denmark and the Netherlands

The Eurasian badger Meles meles has a wide distribution area ranging from Japan to Ireland. In western Europe badger habitats are severely disturbed by anthropogenic factors, leading to fragmentation into subpopulations and formation of a metapopulation substructuring of once continuous panmictic populations. We have examined the genetic structure of Dutch and Danish badger populations on a relatively small scale (within countries) and a larger scale (between countries). The levels of genetic variation of populations were moderate and did not differ significantly among populations (overall H _O=0.30, overall H _E=0.34). Considerable genetic differentiation between the Dutch and Danish populations was found (overall F _ST=0.32, mean pairwise Dutch–Danish F _ST=0.42), indicating a large-scale substructuring of these western European badger populations. Further analysis showed that the Danish badger population can be substructured into three clusters [ P _{( k =3)}=0.99], but the Dutch populations cluster into one more or less panmictic population [ P _{( k =1)}=0.99] with little or no substructuring. The presence of migration barriers, such as roads, together with the peninsular geography of Denmark, may have led to this structuring of badger populations. In contrast, measures that improve migration and connection to other populations from neighboring countries may have prevented substructuring of the Dutch badger population.     

Long-term changes in the feeding pattern of red foxes Vulpes vulpes and their predation on brown hares Lepus europaeus in western Poland

The aim of this study was to estimate long-term changes in the winter feeding pattern of red foxes Vulpes vulpes and in their predation on brown hares Lepus europaeus in relation to the decreasing abundance of hares in western Poland in 1965/1966–2006/2007. The frequencies of occurrence in the stomachs of culled foxes (N?=?726) were used as indices of prey capture rates. The average autumn density of brown hares in the study area decreased from 48 individuals/km² at the turn of the 1960s and 1970s to seven individuals/km² in 1999–2006. Hares and small rodents were the main food classes of foxes in western Poland at the turn of the 1960s and 1970s; however, the occurrence of hares in the fox diet subsequently decreased, and they were replaced by livestock carrion. The relationship between the occurrence frequency of hares in the fox diet and the hare density was best described by sigmoid equation. It indicates that the red fox showed a type III functional response to long-term changes in hare abundance. When predation rate index was estimated on the basis of functional response, the potential fox predation was density-dependent at low to intermediate hare densities (<25 individuals/km²). This finding suggests that the increase in the number of low-density hare populations may require intensive management measures, e.g. simultaneous use of fox control and habitat improvement.     

Seasonal and age changes in the thymus gland of the Red fox, Vulpes vulpes,

Seasonal and age changes in thymus weight and histological structure were examined in the Red fox ( Vulpes vulpes ). Growth in the fox thymus slowed down after birth compared with the last third of foetal existence, but the gland still grew rapidly to reach a peak first year weight when the cubs were 20 weeks of age. From this point the thymus in both sexes decreased markedly in weight to reach a low point by the beginning of the first breeding season. During this involution lobule structure broke down and adipose tissue and connective tissue was laid down in the gland. Recovery of the thymus towards the second year weight maximum was accompanied by the regaining of lobule structure and the gland resembled that of the juvenile again. The male thymus increased in weight from the middle of the mating season, but recovery in the female thymus was delayed until the end of lactation. Involution occurred prior to the second breeding season. Thereafter, the gland never attained the high weights seen in the first two years of life, but histological changes still occurred even in old animals. The thymus gland of animals infected with sarcoptic mange is described.     

Culling-induced changes in badger (Meles meles) behaviour, social organisation and the epidemiology of bovine tuberculosis

In the UK, attempts since the 1970s to control the incidence of bovine tuberculosis (bTB) in cattle by culling a wildlife host, the European badger (Meles meles), have produced equivocal results. Culling-induced social perturbation of badger populations may lead to unexpected outcomes. We test predictions from the 'perturbation hypothesis', determining the impact of culling operations on badger populations, movement of surviving individuals and the influence on the epidemiology of bTB in badgers using data dervied from two study areas within the UK Government's Randomised Badger Culling Trial (RBCT). Culling operations did not remove all individuals from setts, with between 34-43% of badgers removed from targeted social groups. After culling, bTB prevalence increased in badger social groups neighbouring removals, particularly amongst cubs. Seventy individual adult badgers were fitted with radio-collars, yielding 8,311 locational fixes from both sites between November 2001 and December 2003. Home range areas of animals surviving within removed groups increased by 43.5% in response to culling. Overlap between summer ranges of individuals from Neighbouring social groups in the treatment population increased by 73.3% in response to culling. The movement rate of individuals between social groups was low, but increased after culling, in Removed and Neighbouring social groups. Increased bTB prevalence in Neighbouring groups was associated with badger movements both into and out of these groups, although none of the moving individuals themselves tested positive for bTB. Significant increases in both the frequency of individual badger movements between groups and the emergence of bTB were observed in response to culling. However, no direct evidence was found to link the two phenomena. We hypothesise that the social disruption caused by culling may not only increase direct contact and thus disease transmission between surviving badgers, but may also increase social stress within the surviving population, causing immunosuppression and enhancing the expression of disease.     

Size variation of the fox, Vulpes vulpes in the palaearctic region today, and in Israel during the late Quaternary

Fox size variation, both today over a wide geographic range and during the late quaternary in Israel, was correlated with temperature changes. Competition with the related Asiatic jackal was not considered to have any effect on fox size; the degree of dwarfing of the fox was utilized in a speculative estimate of the Pleistocene—Holocene temperature rise.     

Movement of badgers (Meles meles) in a high-density population: individual,population and disease effects.

The movement of 1763 badgers trapped between 36 social groups in Woodchester Park, Gloucestershire, over 18 years was analysed to determine the frequency and duration of moves, the factors associated with a predisposition to move and the spatial pattern of movements. Of those badgers whose capture history could be categorized, nearly half had moved. Of these, 73.1% were classified as ''occasional movers'', 22.1% as ''permanent movers'' and 4.8% as ''frequent movers''. Most adult badgers that moved made occasional moves (78.8%, n = 67). Cubs made all types of move including permanent moves (29%, n = 10). Seventy per cent of females were non-movers compared with 37% of males. Badgers were significantly more likely to move to smaller groups, whereas male badgers were significantly more likely to move to groups with a greater proportion of females. The spatial pattern of movement differed from the distribution of groups with bovine tuberculosis in the study area. However, temporal changes in movement were significantly related to the incidence of Mycobacterium bovis infection in the following year, indicating that as the movement of badgers between groups varies so does the incidence of bovine tuberculosis in the population. This finding is of central importance in the formulation of badger control policy.     

Estimation of parrot and hornbill densities using a point count distance sampling method

The suitability of point count distance methods for estimating densities of tropical parrots and hornbills was assessed during surveys in Indonesia. The methods will perform well, so long as the following are considered. (1) Enough bird records must be accumulated to model species' detection curves precisely. For some species, around 2000 point counts may be needed and, in very rare species, the method may not be appropriate. Pooling data across habitats, species or years may increase precision in cases of small sample size. (2) Point counts are likely to be less biased than line transects because bird detection rates close to the recorder may be higher and there may be less chance of double-counting birds. Distances greater than 400 m between census points are unnecessary. (3) Count periods lasting ten minutes may be needed to ensure that most birds close to the recorder are detected. Controlled flushing of concealed birds after the main count period may also be appropriate. (4) The best time of day for census is the period when bird detectability is high but bird mobility low. For many large avian frugivores, this corresponds to the period between one hour after dawn and 10.30 h. (5) Records of flying birds must be excluded from density calculations. In the species studied, between 2% and 20% should be added to density estimates to compensate for the exclusion of flying birds.     

The role of setts in badger (Meles meles) group size, breeding success and status of TB (Mycobacterium bovis)

This paper examines the relationship between the number of occupied setts in a badger social group territory and badger group size, breeding success, and status of infection with Mycobacterium bovis (TB). The data used were from a long-term epidemiological and ecological study of a high-density population of badgers Meles meles in south-west England. The number of occupied setts in a social group was significantly and positively related to the number of badgers caught in the social group, so that as a social group increases in size, badgers occupy more of the available setts. This relationship remained significant when numbers of adults, adult males and adult females were examined. The number of breeding females, number of cubs and sex ratio was not related to the number of occupied setts in a social group. It is possible that the advantages to breeding females of a larger number of setts available to breed in might be outweighed by the increased aggression found in larger groups. The TB score for prevalence and for incidence of social groups was significantly and positively related to the number of occupied setts in a social group, such that the more occupied setts there were in a territory, the higher the TB index of the group. Possibly the setts themselves contribute to the persistence of TB within social groups, or badgers infected with TB might show a difference in behaviour from uninfected badgers resulting in their increased use of outlying setts.