Escape Tactics and Alarm Responses in Badgers Meles meles: A Field Experiment

A typical badger (Meles meles) territory contains a primary burrow or 'main sett' plus several secondary burrows or 'outlier setts'. The main aim of our study was to test the hypothesis that outlier setts are used as emergency refuges, by subjecting foraging radio-collared badgers to three levels of experimental disturbance (low, moderate and high). In addition, we recorded the occurrence of potential alarm signals. With low-level disturbance, badgers usually returned to the main sett even when this was further away than the nearest outlier sett; with high-level disturbance they always took refuge in the nearest outlier; and with moderate-level disturbance they showed no clear preference. We conclude that outlier setts do act as emergency refuges, but only when an animal is badly frightened. Possible alarm signals (pilo-erection, head-flagging, snorting and growling) occurred mainly during moderate or high-level disturbance but even then they were relatively infrequent. Signals were no more likely to be emitted when conspecifics were near by than when the signaller was alone, and when conspecifics were present they rarely reacted either to the flight of the disturbed animal or to any signals that it emitted. We conclude that such alarm signals as do occur constitute threats directed towards the predator rather than warnings for the benefit of conspecifics.     

Variation in resource presence, utilization and reproductive success within a population of European Badgers (Meles meles)

Variation in resource presence and resource utilization was investigated in a high density population of Badgers in Wytham Woods, Oxfordshire. Earthworms ( Lumbricus terrestris ) contributed the bulk of the diet. Differences between the diet of seven Badger groups were considerable and were most extreme during the summer. Earthworm biomass per habitat remained constant over at least 8 years, while biomass per group territory declined. Pasture fields and mature deciduous woodland (excluding beech-wood) constituted worm-rich, high quality, feeding areas. The combined relative proportion of the area of both habitats per group territory was a good predictor of total group consumption of earthworms and of the reproductive output per group, as measured by the number of independent young, while the dispersion of the two habitats determined the configuration of territories.     

Estimating the impact of past persecution and habitat changes on the numbers of Badgers Meles meles in Britain

Data from a Badger sett survey undertaken in the mid-1980s were used to calculate the effects of past persecution and land-use changes on Badger numbers. The current British Badger population was estimated to be 41,894 ± 4404 social groups; if the effects of past persecution were eliminated, the population could be 43,437 ± 4731 social groups, an increase of 3.7%. Most of this increase relates to persecution in Norfolk and Suffolk last century. In Britain the Badger population is largely confined to those areas which are intensively managed, and the numbers and distribution of Badgers reflect patterns of agricultural activity. However, over-intensive use of the landscape is detrimental to Badger numbers. To quantify the impact of land-use changes on the British Badger population, a number of habitat features favourable to Badgers were identified; 1-km squares that contained five or more such features had significantly higher mean Badger densities. If all the 1-km squares were managed to include five or more of the habitat features favoured by Badgers, and the effects of persecution were eliminated, the Badger population could be 58,284 ± 5640 social groups, an increase of 39%. The absence of semi-natural broadleaved woodlands in a 1-km square had the greatest effect in reducing Badger numbers, and tree-planting schemes may be beneficial in providing potential new sett sites. However, Badgers are poor colonists, and the construction of artificial setts and the translocation of displaced social groups of Badgers will greatly facilitate the colonization process. The value of such an approach for predicting the effects of future land-use policy on Badgers and other species, and for managing the British wildlife resources, is discussed.     

Craniometric variation in the Eurasian badger, Meles meles

A multivariate examination of cranial variation within and between European populations of Meles meles (L.) revealed that populations from Ireland, Great Britain, Norway, and the Slovak Republic could be differentiated both by cranial form and by the degree of sexual dimorphism exhibited. Irish material was characterized by low sexual dimorphism, particularly when compared to Slovak specimens. Badgers from the British Isles had larger skulls than other samples and were more similar to each other than they were to badgers from mainland Europe. Size played a greater role in differentiating samples of female badgers than it did in males. Significant variation occurred within the British Isles, with individual samples being highly differentiable. There was, however, little relationship between morphological similarity and geographic proximity. We contend that macrogeographical (between-country) variation in the species is primarily determined by historical factors and adaptation to current conditions, while microgeographic (within-country) variation is a result of selectively neutral processes.     

Social structure of the Eurasian badger (Meles meles): genetic evidence

Studies of territorial, highly stable groups of wild Eurasian badger, Meles meles , revealed that more than one adult of each sex may breed within a group, and that extra-territorial movements may occur within clusters of territories. Although there is some genetic structuring within a local population and a deficiency of heterozygotes, due probably to minimal juvenile dispersal, heterogeneity of gene frequencies is reduced by: (a) adults transferring between adjacent groups, and (b) matings between males of one group and females of another. Marked changes in gene frequencies between generations indicate that a minority of males have a strong influence on the genotypes of the offspring, being either polygynous or promiscuous. Within one generation, the young of a given group may be sired by two or more males, and these males may not necessarily be members of that group.     

Costs of breeding status in the European badger, Meles meles

Compared with other mammals, reproduction is expected to be particularly costly for European badgers ( Meles meles L.) since both the gestation and mating periods occur in the winter when the animals are inactive and feed little. This paper assesses the costs of breeding status in both male and female badgers, in terms of body condition, ectoparasite load, haematology and mortality. By the end of the lactation period (May), breeding females had suffered a marked loss in body condition, although there was no such cost associated with gestation. However, females regained the weight that they had lost by the autumn following lactation. Lactating two-year-olds experienced a higher age-specific mortality than those that did not breed, but there was no difference among older females. No costs of breeding status could be detected among males at the end of the spring mating period. However, breeding males sustained testicular activity later into the summer than non-breeders, and by the autumn they had acquired more bite wounds and become anaemic. This suggests that there was a physiological cost associated with extended testicular activity in breeding males.     

重引入狗獾释放后定居巢的生境特征

2014年4月—2016年3月,对上海郊区释放的狗獾所建立的洞巢进行了调查。结果表明:异地引入的狗獾在大规模城市化的上海郊区仍能找到合适的栖息地,并能很好地适应野外的自然环境。生境特征分析显示:释放后的狗獾喜好在有地下空间、地势较高的竹林、靠近水源、远离公路的生境中营巢定居;在乔木密度高、草本长势好、远离公路的生境中觅食。狗獾食源地调查显示:上海郊区狗獾冬季主要食物是蚯蚓和土壤昆虫,其主要来源依次为:果林、落叶阔叶林、针叶林、竹林、常绿阔叶林。在上海郊区,重引入狗獾释放成功须满足5个条件:可利用的地下空间,地势较高长势好的竹林,成熟的果林、落叶阔叶林、针叶林提供食物,充足的水源以及避免人为干扰。     

Badger Meles meles setts–architecture, internal environment and function

Badger setts vary considerably in size, ranging from simple single-entrance burrows to complex tunnel systems hundreds of metres long with multiple entrances and underground chambers. Data from 19 excavated setts show that main setts are larger than other setts in terms of area and volume, and contain more chambers, nests and latrines; but setts of different sizes and types are built according to the same basic architectural principles. Little is known about the environmental conditions within setts, other than that temperature and humidity are constant in parts of a sett that are at least 7 m from the nearest entrance. Setts are used for breeding and as sleeping places and refuges, but a question remains as to the functional value of large setts. It is suggested that large main setts allow members of a social group to avoid one another underground, especially when breeding. Little is known about the use of other types of sett.     

Reproductive skew and relatedness in social groups of European badgers, Meles meles

Reproductive skew is a measure of the proportion of individuals of each sex that breed in a group and is a valuable measure for understanding the evolution and maintenance of sociality. Here, we provide the first quantification of reproductive skew within social groups of European badgers Meles meles , throughout an 18-year study in a high-density population. We used 22 microsatellite loci to analyse within-group relatedness and demonstrated that badger groups contained relatives. The average within-group relatedness was high ( R =  0.20) and approximately one-third of within-group dyads were more likely to represent first-order kin than unrelated pairs. Adult females within groups had higher pairwise relatedness than adult males, due to the high frequency of extra-group paternities, rather than permanent physical dispersal. Spatial clustering of relatives occurred among neighbouring groups, which we suggest was due to the majority of extra-group paternities being attributable to neighbouring males. Reproductive skew was found among within-group candidate fathers ( B  = 0.26) and candidate mothers ( B  = 0.07), but not among breeding individuals; our power to detect skew in the latter was low. We use these results to evaluate reproductive skew models. Although badger society best fits the assumptions of the incomplete-control models, our results were not consistent with their predictions. We suggest that this may be due to female control of paternity, female–female reproductive suppression occurring only in years with high food availability resulting in competition over access to breeding sites, extra-group paternity masking the benefits of natal philopatry, and/or the inconsistent occurrence of hierarchies that are linear when established.     

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.