Lunar-related reproductive behaviour in the badger (Meles meles)

Cyclicity in behaviours, including reproduction, in relation to the lunar cycle is widely documented in some phyla, but weak or unknown in Class Mammalia. In this paper we present long-term video surveillance data of wild Eurasian badgers Meles meles, which reveal a strong correlation between reproductive behaviour and the lunar cycle. Squat marking and raised-leg urination, which increase in frequency at times of reproductive activity, showed maxima around day 22 of the lunar cycle (i.e. new moon). These findings were supported by observations of matings, together with published records, which showed significantly higher occurrence in the lunar dark phase (last quarter to first quarter). We propose that the lunar cycle has the potential to act as a regulator of the reproductive cycle in the badger.     

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 dimorphism in the skull of minks Mustela vison, badgers Meles meles and otters Lutra lutra

Multiple-group principal component analysis and discriminant analysis were used to investigate the morphological differences between adult skulls of male and female minks, badgers and otters from Norway. The first principal component axis, calculated from the variance-covariance matrix of log-transformed data, was interpreted as a growth-free size axis in all three species, while the other components were interpreted as representing shape. Having largely separated size and shape variation, these two aspects of sexual dimorphism could be studied. The standardized component scores were subjected to an analysis of variance and discriminant analyses were performed on size-in and size-out data. Sexual dimorphism was disclosed on eight of the 12 components in minks and on seven of the 12 components in badgers and otters. In mink the multivariate differences were more due to size than to shape, whereas in badgers and otters most of the multivariate differences were due to shape, but the differences in size were also significant. The shape dimorphism was shown to be functionally related to jaw and neck muscles. The results were discussed in relation to recent theories to explain the evolutionary significance of sexual dimorphism in body size of mustelids. It was concluded that these theories do not fully explain the dimorphism found in the skulls of the moderately dimorphic badger and otter.     

The effects of weather conditions on the movements and activity of badgers (Meles meles) in a suburban environment

This study provides quantitative data relating short-term fluctuations in local weather conditions to various measures of badger activity. These relationships were examined on a yearly, quarterly and monthly basis using behavioural data collected from 65 animals radio-tracked for a total of 518 nights in the suburbs of north-west Bristol. The yearly pattern of badger activity was reflected in a strong positive correlation between activity and daylength; in addition, moonlight and the absence of cloud cover were shown to restrict both the speed of travel and nightly range size, and to delay emergence. Looking at the data on a quarterly basis, activity increased with increasing temperature in the spring and autumn. Heavy rain reduced above-ground activity in the autumn, and in the winter speed of travel increased with wind speed. Nutritionally stressed adult females showed an increase in activity during the shorter summer nights. However, in general, changes in badger activity could not be readily predicted on the basis of the weather variables measured. The significance of these relationships is discussed in the light of the behaviour of badgers living in suburban Bristol.     

The first report of Aelurostrongylus falciformis in Norwegian badgers (Meles meles)

The first report of Aelurostrongylus falciformis (Schlegel 1933) in Fennoscandian badgers is described. Routine parasitological examination of nine Norwegian badgers, at the National Veterinary Institute during 2004 and 2005, identified A. falciformis in the terminal airways of five of the animals. The first stage larvae (L1) closely resembled, in size and morphology, those of Angiostrongylus vasorum (Baillet 1866). The diagnosis for both A. falciformis and A. vasorum is frequently based on the identification of L1 in faeces or sputum. The potential for misclassification of an A. falciformis infection as A. vasorum, where larval identification is the only diagnostic method used, is discussed.