Distribution and population density of badgers Meles meles in Luxembourg

1. The distribution and density of Eurasian badgers Meles meles in Luxembourg was estimated by gathering information about the location of badger setts with a questionnaire survey, by visiting 708 setts in order to classify them as ‘main setts’ or ‘outliers’, and by estimating social group size by directly counting emerging badgers. 2. Badgers were found to be widely distributed in Luxembourg, with a minimum main sett density of 0.17 setts/km². Setts were sited preferentially in forest habitat. The mean minimum group size was 4.6 badgers. 3. The Luxembourg badger population was conservatively estimated to contain at least 2010 adult and young badgers (95% CI 1674–2347) in spring 2002, equivalent to a density of 0.78 adult and young badgers/km² (95% CI 0.65–0.91). This is moderate compared to most of continental Europe.     

Resource dispersion and badger population density in Mediterranean woodlands: is food,water or geology the limiting factor?

Eurasian badgers, Meles meles, in Mediterranean cork‐oak woodlands live in small groups within territories that embrace a mosaic of habitats where several setts (dens) are scattered. Assuming that their population density was related to home range sizes and that this in turn was influenced by food and water availability and the existence of substrate suitable for sett construction, we explored the relationship between these parameters. Two biotopes were predominantly important in providing food security to badgers in the ‘Grândola’ mountain study area: olive groves and orchards or vegetable gardens. Analysis of the mean total area of these two habitats in the ranges of radio‐tracked badgers permitted us to extrapolate to an estimate that the 66 km² encompassed eleven areas with the capacity to support badger groups each composed by 6–8 individuals. Since only three groups populated the area we concluded that food availability was not limiting badger density. Sites with surface water in summer (the dry season) seem sufficient to support more badger groups than existed, leading us to believe that this factor was also not limiting badger density. Simultaneously, using a logistic regression model and the biophysical characteristics of sett sites as explanatory variables, four predictor variables determined sett location: the existence of a geological fault/discontinuity, ridges, valleys and the distance to abandoned farm houses, of which the former had the higher odds ratio, being thus the best sett location predictor. Indeed, 56% of the areas predicted with >80% confidence to contain a badger sett were encompassed within a known home range. Therefore, our results suggest that, in Mediterranean cork oak woodlands in SW Portugal, the main factor limiting badger's density is the availability of suitable sites for setts. However, in areas where suitable sites for burrows existed, but food patches were absent, badgers were not found. This could indicate that the presence of both factors was necessary for badgers, although in this area sites suitable for digging setts appeared to be the primary limiting factor.     

Evaluating seasonal bait delivery to badgers using rhodamine B

In the UK and Ireland, research on the control of bovine tuberculosis in badgers includes the development of a palatable bait for oral delivery of a vaccine and a means of its deployment in the field. In the present study, we carried out field deployment of bait according to the established method of bait marking in early spring and early summer to compare the effects of seasonality on bait uptake rates. All baits contained rhodamine B (RhB) which was subsequently detected in the hair and whiskers of captured badgers. During the 8 days of bait feeding at 14 badger setts, 99% of baits deployed in spring, and 100% of those deployed in summer were removed. The presence of RhB in captured badgers indicated high rates of uptake amongst adult badgers in spring (93%) and summer (98%). Only cubs captured in summer showed evidence of having taken bait (91%). Between 67% and 100% of each social group was estimated to have taken bait. The detection of RhB in 96% of badgers captured at outlier setts, where bait was not fed, suggested that deployment at main setts alone may be sufficient to target a relatively high proportion of the badger population. The number of baits deployed per marked badger suggested that a similar level of uptake might be achievable using fewer baits. The results clearly demonstrate the potential value of the bait-marking methodology for delivering vaccine baits to badgers during spring and summer, but that deployment in early summer is necessary to target cubs.     

Annual and circadian activity patterns of badgers (Meles meles) in Białowieża Primeval Forest (eastern Poland) compared with other Palaearctic populations

Aim The annual and circadian rhythms and duration of activity of Eurasian badger Meles meles (Linnaeus 1758) were studied in a low‐density population inhabiting the primeval woodland in the European temperate zone. Results were compared with available data from the literature on seasonal changes in body mass and winter inactivity of badgers from across the Palaearctic region. Location Field work was carried out in Bia?owie?a Primeval Forest, eastern Poland. Biogeographical variation was reviewed based on twenty‐three localities in the Palaearctic region (from Western Europe to Central Siberia). Methods Thirteen badgers were radio‐collared in 1997–2001. Their circadian activity was sampled by 24‐h sessions of continuous radio‐tracking with location taken at 15‐min intervals. Annual activity was studied by radio‐tracking and inspections of setts. Earthworm (badgers’ main food) biomass was estimated in four types of habitats throughout the year. Results Badgers were nocturnal with one long bout of activity. Their rhythms of diel activity differed between spring and autumn, and between adult and subadult individuals. On average, badgers emerged from setts at 19:00 hours and returned to them at 03:42 hours. The highest level of activity was recorded between 20:00 and 03:00 hours. Duration of daily activity was, on average, 8.2 h day^?1, but varied significantly between seasons. The seasonal changes were inversely related to the abundance of earthworms. Duration of activity also depended on daily temperature, especially in the cold season. In winter, badgers stayed inactive for an average of 96 days per year. In autumn, they built fat reserves and their body mass nearly doubled compared with the spring values. The literature review on annual cycle of activity and body mass changes in Eurasian badgers showed that fat storage and duration of winter sleep strongly depended on climate (best approximated by January mean temperature). In regions with warm climates, badgers were active year round and their body mass changed only slightly, while in regions with severe winters badgers increased their body mass twofold from spring to autumn, and stayed inactive for as long as 6 months per year. Main conclusion We propose that, in the temperate and boreal zones of the Palaearctic region, the ultimate determinant of biogeographical variation in badgers’ annual activity is the winter shortage of earthworms, which are the main component of badger diet.     

The density and distribution of badger setts in the Sudety Mountains,Poland

The density and distribution of badgerMeles meles (Linnaeus, 1758) setts was estimated by questionnaires and field studies, carried out in the Sudety Mountains between 1995–2002. The questionnaire referred to the whole territory of Polish Sudety Mts, while field studies were conducted in four different habitat types: low mountains with a mosaic farm-forest landscape, highly industrialised hilly areas, high mountain ranges of natural character and high mountain ranges of severe microclimate and heavily destroyed tree stands. On the basis of both questionnaires and field surveys, a total of 378 badger setts, classified according to their size and status, were identified. Among these, 119 (31.5%) were situated on three areas, while in the fourth area we did not find any badger setts. According to their size and traces of intensive occupation, 54 setts were regarded as main badger setts. The mean density of main setts on three areas was much the same and amounted to 0.05–0.07/km² of their total surface, despite differences in their natural environment and agricultural or industrial changes in landscapes. In the Sudety Mts badgers selected settlements in forest habitats, bordering rich in food open areas. The density of main setts in forest areas ranged from 0.12 to 0.33/km² depending on the proportion of forest, type and age of tree stands and size of forest complexes. The mean distance of main setts from open areas ranged from 209 to 280 m. The mean nearest neighbour distance (NND) between main setts ranged from 2.85 to 3.75 km. The home range size estimated for a social group varied from 7.9 to 13.6 km². The highest occupied setts of our study were found on the ?nie?nik Massif, at an altitude of 700 m a.s.l.     

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.     

Defecation and urination patterns of badgersMeles meles at low density in south west England

The spatial distribution of urine and faecal scent marks of badgersMeles meles (Linnaeus, 1758) at low population density (mean±SE across 4 social groups was 5.73±0.735 badgers/km2) in south-western England were quantified. Eighteen badger latrines (greater than one dung pit containing faeces), 74 single defecations not in pits and 21 faeces in single pits were located in spring when badgers were defending well-defined territories. Woodland was selected, and arable land avoided, for latrine sites. Pasture and built-up land was selected for single defecations not in pits whereas faeces in single pits were distributed randomly across habitat types. Faecal scent marks were strongly associated with the edge of pastoral fields rather than the middle. Forty-six and 51 urinations were located in spring and summer, respectively. Urine was deposited randomly across habitat types but was concentrated at the linear features surrounding the main setts. This is the first reported use of high levels of single defecations and urinations in badger scent marking strategies in the UK. These results are discussed in relation to the potential for transmission of bovine tuberculosisMycobacterium bovis from badger excreta to cattle.     

Impact of culling on relative abundance of the European badger (Meles meles) in Ireland

The European Badger (Meles meles) has been implicated in the epidemiology of bovine tuberculosis in cattle populations in the Republic of Ireland. Badger populations have been subject to a culling regime in areas with chronic histories of bTB cattle herd breakdowns. Removal data from 2004 to 2010 were used to model the impact of culling on populations in areas under capture. Additionally, changes in field signs of badger activity were used as an index of abundance to support, or otherwise, the outcomes of the removal models. Significant reductions in standardised badger captures over time were found across three large study areas (total area, 1,355 km²). Assuming that all inactive setts were vacant, an overall linear trend model suggested that badger captures had decreased by 78 % for setts with 6 years of repeated capturing operations. Given the uncertainty associated with the relationship between sett activity and badger presence, we repeated the linear modelling using two ‘what if’ scenarios. Assuming that individual badgers were missed on 10 % or 20 % of occasions at inactive setts, the estimated decline over 6 years is lowered to 71 % or 64 %, respectively. The decline profile consisted of a steep initial decrease in captures within the first 2 years, followed by a more gradual decrease thereafter. The number of active openings at setts (burrows) declined significantly in all three areas; but the magnitude of this decline varied significantly amongst study areas (41–82 %). There was a significant increase in the probability of setts becoming dormant with time. The removal programme was more intense (mean, 0.45 badgers culled km^?2 year^?1) than previous experimental badger removals in Ireland but some captures may be attributed to immigrant badgers as no attempt was made to limit inward dispersal from areas not under management. Results from this study suggest that significant reductions in badger density occurred in the areas where management had taken place. Since other non-culled badger populations in Northern Ireland and Britain exhibited stable population trends, we attribute the reduction in relative abundance to the culling regime. Further studies of the dynamics of this reduction are required to quantify how it is counteracted by immigration from populations outside of culled areas.     

The German wildlife information system (WILD): population densities and den use of red foxes (<Emphasis Type="Italic">Vulpes vulpes</Emphasis>) and badgers (<Emphasis Type="Italic">Meles meles</Emphasis>) during 2003–2007 in Germany

Monitoring the populations of badgers and red foxes may help us to manage these predator species as a matter of wildlife conservation and regulation. To fit the needs of a monitoring programme, the most practicable method has to be selected. Hunting bag statistics deliver large but inaccurate data amounts with low effort. Indirect and also often direct counts might deliver only presence–absence data with high effort. Direct counts with high accuracy are very costly. Den mapping by volunteer local hunters can deliver reliable data on density and additional biological variables while being feasible and cost effective. Within reference areas all over Germany, fox and badger dens and litters were recorded, and spring and summer densities estimated as well as potential annual population increases were calculated for 2003–2007. Habitat preferences for breeding dens were also analysed. Additionally, in 2006, the distribution of badgers was surveyed by a nationwide questionnaire. Fox and badger are distributed all over Germany with some small gaps and regionally differing densities. During the monitoring period, fox and badger densities and reproduction stayed stable, at a high level corresponding to hunting bags. However, densities varied between geographical regions, with lower densities in the sparsely wooded lowland regions. A preference for forest and habitats offering shelter was clear for breeding setts and dens. Badgers especially preferred setts of natural origin.     

Urban badger setts: characteristics, patterns of use and management implications

Damage caused by badger setts is an important source of human–carnivore conflict in urban areas of the UK, yet little is known about the spatial distribution of urban badger setts or their pattern of occupation. We compared the density, spatial distribution and size of setts in four urban and two rural study areas in the UK and assessed the applicability to urban systems of distinguishing between 'main' and 'outlier' setts. In addition, we used radio-telemetry to investigate diurnal patterns of sett use in one urban area (Brighton). It was possible to distinguish between main and outlier setts in urban environments, and local sett densities were comparable in urban and rural areas. However, urban badgers used substantially fewer setts than did a nearby rural population, and they spent a smaller proportion of days in outlier setts. Social groups with larger ranges had more setts available to them and, within groups, individuals with larger ranges used more setts. Outliers appeared to serve multiple functions, including allowing efficient and safe travel to important parts of the home range. We conclude that sett densities can be high in urban habitats, suggesting significant potential for sett-related problems to arise. The fact that urban main setts can be distinguished from outliers enables management actions to be tailored accordingly. In particular, because main setts seem to represent a particularly valuable resource to urban badgers, alternatives to the closure of problem main setts need to be considered.     

狗獾夜间活动节律是受人类活动影响而形成的吗?基于青海湖地区的研究实例

青海湖地区是目前已知的狗獾分布海拔最高点。为了解狗獾在青藏高原严酷生态环境下的生活史特点, 并验证是否人类干扰造成了狗獾夜行性的假说, 我们利用红外相机技术, 结合无线电遥测和野外调查研究了青海湖湖东地区亚洲狗獾(Meles leucurus)的种群密度、洞穴口的行为及活动节律。结果表明: (1)研究地区狗獾的平均种群密度为1.2 ± 0.6只/km², 其分布受食物丰富度的影响; (2)狗獾基本在夜间活动, 出洞时间集中在20:00-23:00之间, 而回洞时间则集中在清晨4:00-7:00之间, 23:00-4:00之间是狗獾的活动高峰; (3)狗獾离洞前行为主要是警戒行为, 回洞穴时的行为主要是嬉戏行为, 其他行为较少见, 表达具有特定的时间性; (4)人类活动对于狗獾活动没有显著性影响(P < 0.05)。     

Interspecific visitation of cattle and badgers to fomites: A transmission risk for bovine tuberculosis?

In Great Britain and Ireland, badgers (Meles meles) are a wildlife reservoir of Mycobacterium bovis and implicated in bovine tuberculosis transmission to domestic cattle. The route of disease transmission is unknown with direct, so‐called “nose‐to‐nose,” contact between hosts being extremely rare. Camera traps were deployed for 64,464 hr on 34 farms to quantify cattle and badger visitation rates in space and time at six farm locations. Badger presence never coincided with cattle presence at the same time, with badger and cattle detection at the same location but at different times being negatively correlated. Badgers were never recorded within farmyards during the present study. Badgers utilized cattle water troughs in fields, but detections were infrequent (equivalent to one badger observed drinking every 87 days). Cattle presence at badger‐associated locations, for example, setts and latrines, were three times more frequent than badger presence at cattle‐associated locations, for example, water troughs. Preventing cattle access to badger setts and latrines and restricting badger access to cattle water troughs may potentially reduce interspecific bTB transmission through reduced indirect contact.     

Restricted ranging behaviour in a high-density population of urban badgers

By studying the responses of different species to urbanization, it is possible to understand the impact of this type of habitat modification and to explore, more generally, the link between variations in the environment and changes in behaviour. We radio collared 17 badgers Meles meles from six social groups in a 1 km² urban study area in Brighton, UK, where local badger population density was high, and collected data on their ranging behaviour between 2005 and 2007. We aimed to determine how badgers adapt their behaviour to an urban environment and to assess the generality of previously reported differences in the ranging and territorial behaviour of urban and rural badgers. Analysis of habitat preferences and movement patterns suggested that garden habitat was principally used for foraging, while scrub and allotment habitats were important in allowing animals to travel from one part of their range to another. Group and individual home ranges were the smallest so far recorded for badgers (mean 100% minimum convex polygons=9.26 and 4.91 ha, respectively). Individual range size was negatively correlated with the availability of garden habitat, suggesting that the rich food resources provided by gardens enabled ranges to be small. Group ranges were mostly non-contiguous and there was no evidence of territorial scent marking; rather, activity was mainly restricted to areas in the vicinity of main setts. It is clear that badgers can adapt successfully to urban habitats and that this process affects various aspects of their behaviour. However, our high-density population of urban badgers displayed patterns of behaviour that differed not only from those of typical rural badgers, but also in some respects from those of a previously studied low-density urban population. We conclude that generalizations about the effects of urbanization must be made with caution.     

Weather influences trapping success for tuberculosis management in European badgers (<Emphasis Type="Italic">Meles meles</Emphasis>)

European badgers (Meles meles) in Ireland and the UK are a reservoir for Mycobacterium bovis, the causative agent of bovine tuberculosis (TB). A number of interventions have been evaluated in attempts to control bovine TB within badger populations, and many of which rely on the capture of badgers. One strategy being implemented within Ireland is intramuscular vaccination using Bacillus Calmette-Guérin (BCG), as an alternative to badger culling. The success of vaccination as a disease control strategy depends on the ability to capture badgers and administer vaccines; thus, trapping success is crucial to effectively vaccinate the population (maximize vaccine coverage). A field vaccine trial was conducted in County Kilkenny, Ireland, from 2010–2013. We used data from this trial to evaluate the association between weather (precipitation and temperature data), badger sett characteristics, and badger trapping success. Approximately 10% of capture efforts resulted in a badger capture. Our results indicate that badger captures were the highest in drizzle, rain, and heavy rain weather conditions, and when minimum temperatures ranged from 3–8 °C. Badger captures were the highest at main setts (large burrow systems), and when sett activity scores were high (qualitative classes 4 or 5). Using local precipitation and temperature data in conjunction with observed sett characteristics provides wildlife managers with guidelines to optimize trapping success. Implementing capture operations under optimal conditions should increase the trapping success of badgers and allow for increased delivery of vaccines to manage bovine TB.     

The distribution of Eurasian badger, Meles meles, setts in a high-density area: field observations contradict the sett dispersion hypothesis

Are setts significant determinants of badger socio‐spatial organisation, and do suitable sett sites represent a limited resource, potentially affecting badger distributions? The factors determining diurnal resting den, or sett, location and selection by Eurasian badgers Meles meles L. were investigated in Wytham Woods, Oxfordshire. 279 sett sites were located. The habitat parameters that were associated with the siting of these setts were analysed and associations were sought between sett location and character and the body condition and body weight of resident badgers Habitat characteristics in the vicinity of setts were significantly different from randomly selected points. Badgers preferentially selected sites with sandy, well‐drained soils, situated on NW‐facing, convex and moderately inclined slopes at moderate altitude. There was no evidence that sett morphology (number of entrances, sett area, number of hinterland latrines) was affected by the surrounding sett site habitat characteristics. Mean body weight was significantly higher for badgers occupying territories with setts in sandy soils, situated on NW‐facing slopes, than in territories with less optimal sett characteristics. Contrary to the hypothesis that the availability of sett sites was limiting, and therefore that sett dispersion dictates the spatial and social organisation of their populations, the badgers were clearly able to excavate new setts. On our measures, these new setts were not inferior to old established ones, despite occupying subsequently exploited sites; the badgers utilising these new setts had neither lighter body weights nor poorer body condition scores. During the period of our study badgers have manifestly been able to dig numerous new setts; as satisfactory sites still remain available, this indicates that suitable sett sites have not yet become a limiting resource. There was no relationship between sett age and the characteristics of the site in which it was dug, as suitable sites were not limiting. Significantly, population expansion during the decade 1987–1997 was not constrained by lack of setts, rather the main proliferation in setts occurred after the population size had peaked in 1996. Some implications for the management and conservation of the Eurasian badger are considered.     

Seasonal and spatial pattern of shelter use by badgers<Emphasis Type="Italic">Meles meles</Emphasis> in Białowieża Primeval Forest (Poland)

In 1997–2001, we investigated the use of day-time shelters by radio-collared badgersMeles meles (Linnaeus, 1758) in the Białowieża Primeval Forest, eastern Poland. Each social group of badgers utilised, on average, 9 different shelters per territory (range: 4–20). The main setts, occupied for breeding and winter sleep, were also most frequently used for day-time rest throughout the year (73% of days). Badgers living in the pristine oldgrowth stands utilised larger number of shelters and spent more days in hollow trees (mainly limeTilia cordata), compared to badgers inhabiting younger secondary tree stands. Number of shelters used by individuals varied between seasons and depended on sex and age of animals. In summer, badgers used more shelters than in spring and autumn. In winter, they stayed in their main setts only. Adult males occupied more shelters and spent fewer days in the main sett than other badgers. In spring, females rearing young used only the main setts. The average underground space used by badgers within the main sett was 128 m². It was largest in summer and smallest in winter, and also varied between males and females. We proposed that, in a low-density population, badgers used several setts and other daily shelters to reduce energy expenditure when exploring their large territories and foraging. Furthermore, setts may play a role of marking sites. Analysis of the biogeographical pattern of sett use by European badgers showed that the number of setts used by social groups increased with increasing territory size, whereas the density of setts (n setts/km²) was negatively correlated with territory size. We proposed that different factors could shape the utilisation of setts by badgers in low- and high-density populations.     

Spatial Targeting for Bovine Tuberculosis Control: Can the Locations of Infected Cattle Be Used to Find Infected Badgers?

Bovine tuberculosis is a disease of historical importance to human health in the UK that remains a major animal health and economic issue. Control of the disease in cattle is complicated by the presence of a reservoir species, the Eurasian badger. In spite of uncertainty in the degree to which cattle disease results from transmission from badgers, and opposition from environmental groups, culling of badgers has been licenced in two large areas in England. Methods to limit culls to smaller areas that target badgers infected with TB whilst minimising the number of uninfected badgers culled is therefore of considerable interest. Here, we use historical data from a large-scale field trial of badger culling to assess two alternative hypothetical methods of targeting TB-infected badgers based on the distribution of cattle TB incidents: (i) a simple circular ‘ring cull’; and (ii) geographic profiling, a novel technique for spatial targeting of infectious disease control that predicts the locations of sources of infection based on the distribution of linked cases. Our results showed that both methods required coverage of very large areas to ensure a substantial proportion of infected badgers were removed, and would result in many uninfected badgers being culled. Geographic profiling, which accounts for clustering of infections in badger and cattle populations, produced a small but non-significant increase in the proportion of setts with TB-infected compared to uninfected badgers included in a cull. It also provided no overall improvement at targeting setts with infected badgers compared to the ring cull. Cattle TB incidents in this study were therefore insufficiently clustered around TB-infected badger setts to design an efficient spatially targeted cull; and this analysis provided no evidence to support a move towards spatially targeted badger culling policies for bovine TB control.     

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.     

The behavioural responses of badgers (Meles meles) to exclusion from farm buildings using an electric fence

Behavioural investigations into the transmission of bovine tuberculosis (Mycobacterium bovis) between badgers and cattle suggest that badger activity in farm buildings may incur a significant risk of cross-infection. However, measures to exclude badgers from buildings have not been systematically field-tested. In the present study, remote surveillance and radio-tracking were used to monitor the effect of electric fencing manipulations on the frequency of badger incursions into feed stores and cattle housing, and on badger ranging behaviour. Electric fencing was effective in preventing access to the farm buildings where it was installed and also significantly reduced incursions into unfenced buildings. Badger home range and core activity areas tended to increase in size when the fencing was installed, although they did not extend beyond the boundaries of the relevant social group territories. We discuss the logistical constraints of using electric fencing in this context and conclude that it is a potentially useful method of reducing contact between badgers and cattle, within farm buildings and yards.     

Changes in the prevalence of badger persecution in Northern Ireland

Animal populations generally increase after release from hunting pressure and/or cessation of illegal persecution. Implementation of full legislative protection of the Eurasian badger Meles meles in Great Britain is thought to have led to increases in badger abundance due to reduced levels of persecution. Conversely, prevalence of badger persecution in Northern Ireland was historically much higher than in Great Britain, and badger abundance remained stable over time despite similar legislative protection. We examined temporal changes in the prevalence of badger sett disturbance in Northern Ireland from 1990/1993 to 2007/2008 in relation to population status. A total of 56 (12.6%) of 445 setts surveyed during 1990/1993 had been disturbed compared to 29 (4.4%) of 653 setts during 2007/2008. This was a significant decline (−65%) in the incidence of sett disturbance over the 14–18-year period. Most notably, the incidence of digging at badger setts, indicative of local badger baiting activity, declined from 50% to 3.5% of disturbed setts. Signs of recent disturbance were significantly more frequent at disused setts suggesting that once disturbed, badgers may vacate a sett. The number of badger social groups in Northern Ireland did not differ between the two study periods, suggesting that previously high levels of badger persecution did not limit the number of badger social groups. The stability of the badger population in Northern Ireland compared to the growing population in Great Britain cannot be attributed to changes in the prevalence of persecution. Differences in the trajectories of both populations could be due to a range of factors including climate, habitat composition and structure, farming practices or food availability. More work is needed to determine how such factors influence badger population dynamics.