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.     

Acute disseminated toxoplasmosis in a red fox (Vulpes vulpes)

A red fox (Vulpes vulpes) with signs of neurological disease was captured in Fairmount Park, Philadelphia, Pennsylvania (USA). The animal died in captivity and was examined because of suspected rabies. The liver had pale foci up to 4 mm in diameter. Foci of necrosis were associated with Toxoplasma gondii tachyzoites in several organs including liver, lungs and adrenal glands. Rabies antigen and distemper virus inclusions were not detected. The diagnosis of acute disseminated toxoplasmosis was confirmed by immunohistochemical staining.     

Identification of the Tibetan fox (Vulpes ferrilata) and the red fox (Vulpes vulpes) by copro-DNA diagnosis

Studies on feeding habits based on faeces dissecting are imperative to understand the natural history of Tibetan foxes and their functions in the transmission of a lethal zoonotic parasite, Echinococcus multilocularis. However, Tibetan foxes and red foxes live sympatrically on the Tibetan plateau, China. Therefore, the faeces of Tibetan foxes must be distinguished from those of red foxes. We established a diagnostic method to distinguish the faeces of the two species by amplifying a portion of the mitochondrial cytochrome b gene (cytb) and digesting with the restriction enzymes BamHI and SspI, to produce specific diagnostic banding patterns. This PCR-RFLP assay enabled rapid, accurate and easily performed identification and differentiation of the two species.     

Successful embryo transfer in the silver fox (Vulpes vulpes)

Surgical embryo transfer in the silver fox was investigated as part of a larger project concerning the conservation of endangered canine species using modern artificial reproduction techniques with the farmed fox as a model. The animals were chosen on the basis of synchrony in natural oestrus. The timing of ovulation and artificial insemination was determined by measuring electrical resistance in the vagina. Twenty-nine embryos were flushed from eight humanely killed donor females and transferred surgically into the uteri of eight recipients. One recipient female gave birth to two male pups 47 days after the transfer of four expanded blastocysts and one embryo at the 16-cell stage derived from a donor female flushed 10 days after artificial insemination.     

Systemic AA amyloidosis in the red fox (Vulpes vulpes)

Amyloid A (AA) amyloidosis occurs spontaneously in many mammals and birds, but the prevalence varies considerably among different species, and even among subgroups of the same species. The Blue fox and the Gray fox seem to be resistant to the development of AA amyloidosis, while Island foxes have a high prevalence of the disease. Herein, we report on the identification of AA amyloidosis in the Red fox (Vulpes vulpes). Edman degradation and tandem MS analysis of proteolyzed amyloid protein revealed that the amyloid partly was composed of full‐length SAA. Its amino acid sequence was determined and found to consist of 111 amino acid residues. Based on inter‐species sequence comparisons we found four residue exchanges (Ser31, Lys63, Leu71, Lys72) between the Red and Blue fox SAAs. Lys63 seems unique to the Red fox SAA. We found no obvious explanation to how these exchanges might correlate with the reported differences in SAA amyloidogenicity. Furthermore, in contrast to fibrils from many other mammalian species, the isolated amyloid fibrils from Red fox did not seed AA amyloidosis in a mouse model.     

Responses of small mammals to Red fox (Vulpes vulpes) odour

This paper describes the responses of three species of rodents (Apodemus sylvaticus, Microtus agrestis and Clethrionomys glareolus) and a shrew (Sore.x araneus) to traps tainted with the faecal odour of a predator, the Red fox. The rodents generally avoided traps bearing fox odour, but readily entered traps marked with rodent odour, whereas shrews entered all traps equally. Among the rodents, avoidance of fox odour was strongest in male A. sylvaticus and C. glareolus and least in M. agrestis and female A. sylvaticus . Fox droppings were found principally along paths and in open habitats where, of the rodents mentioned, they were most likely to be encountered by A. sylvaticus . It was suggested that avoidance of fox faecal and urinary odours in this species, especially by the active males, would reduce the time spent in areas frequented by foxes, and hence reduce the chance of encountering the predator itself. In contrast, M. agresis would seldom encounter fox droppings in its sub-surface runways, so avoidance of fox faecal odour would do little to reduce its chance of encountering the predator. Avoidance by the rodents of the faecal odour of badger, a predator not present in the study areas, was only slightly less marked than their avoidance of fox faecal odour. It was postulated that similar chemicals eliciting avoidance in rodents may commonly occur in the faeces and urine of carnivores.     

The impact of sarcoptic mange Sarcoptes scabiei on the British fox Vulpes vulpes population

• 1 Disease epizootics can significantly influence host population dynamics and the structure and functioning of ecological communities. Sarcoptic mange Sarcoptes scabiei has dramatically reduced red fox populations Vulpes vulpes in several countries, including Britain, although impacts on demographic processes are poorly understood. We review the literature on the impact of mange on red fox populations, assess its current distribution in Britain through a questionnaire survey and present new data on resultant demographic changes in foxes in Bristol, UK.
• 2 A mange epizootic in Sweden spread across the entire country in < 10 years resulting in a decline in fox density of up to 95%; density remained lowered for 15–20 years. In Spain, mange has been enzootic for > 75 years and is widely distributed; mange presence was negatively correlated with habitat quality.
• 3 Localized outbreaks have occurred sporadically in Britain during the last 100 years. The most recent large‐scale outbreak arose in the 1990s, although mange has been present in south London and surrounding environs since the 1940s. The questionnaire survey indicated that mange was broadly distributed across Britain, but areas of perceived high prevalence (> 50% affected) were mainly in central and southern England. Habitat type did not significantly affect the presence/absence of mange or perceived prevalence rates. Subjective assessments suggested that populations take 15–20 years to recover.
• 4 Mange appeared in Bristol's foxes in 1994. During the epizootic phase (1994–95), mange spread through the city at a rate of 0.6–0.9 km/month, with a rise in infection in domestic dogs Canis familiaris c. 1–2 months later. Juvenile and adult fox mortality increased and the proportion of females that reproduced declined but litter size was unaffected. Population density declined by > 95%.
• 5 In the enzootic phase (1996–present), mange was the most significant mortality factor. Juvenile mortality was significantly higher than in the pre‐mange period, and the number of juveniles classified as dispersers declined. Mange infection reduced the reproductive potential of males and females: females with advanced mange did not breed; severely infected males failed to undergo spermatogenesis. In 2004, Bristol fox population density was only 15% of that in 1994.

     

Short microsatellite DNA markers for the red fox (Vulpes vulpes)

Seven short microsatellite loci (< 165 bp) were characterized for red foxes for the amplification of degraded DNA extracted from historical samples. Following polymerase chain reaction (PCR) using primers developed in the domestic dog, red fox‐specific primers were designed within the flanking regions. The number of detected alleles ranged between six and 15 alleles and the expected heterozygosities ranged between 0.67 and 0.92. No deviations from Hardy–Weinberg equilibrium were detected for any of the markers.     

Photoperiodic regulation of reproduction in the male silver fox (Vulpes vulpes)

Six silver fox males were exposed to short days (6L:18D) from February, when the testes were fully developed, until June 1986 (Group 6L). Eight males maintained in natural daylight served as controls (Group N). Histological sections from the testes of 2 males in Group 6L killed in June indicated full spermatogenic activity. Three blue fox vixens inseminated the following year with semen collected and frozen in June from 3 males in Group 6L failed to produce litters. One possible explanation for the reproductive failures could have been that the high environmental temperatures in June influenced semen quality. There was no significant difference (P greater than 0.05) in LH release in response to GnRH stimulation in June, but testosterone response to LH release was significantly higher (P less than 0.01) in animals subjected to a restricted photoperiod, demonstrating that testicular testosterone production was maintained longer than in control animals. Two males in Group 6L were retained in 6L:18D from June until December 1986 and then exposed to natural daylight until the end of the study in May 1987 (Group 6L:6L:N). These males started to shed their winter coat and showed clinical signs of testicular regression in December, i.e. after approximately 11 months exposure to 6L:18D. The 2 remaining males in Group 6L were moved to cages with natural daylight in June 1986, where they were kept until the end of the experiment (Group 6L: N:N). These males displayed testicular regression soon after the change in photoperiod but maintained their capacity for testicular redevelopment during the following breeding season.(ABSTRACT TRUNCATED AT 250 WORDS)     

Multivariate geographical variation of the Red fox (Vulpes vulpes) in Wales

Seven different cranial measurements of foxes of known sex were recorded. Univariate and multivariate techniques were used to study the geographical variability of the skulls. A clear multivariate separation of skulls from six counties in Wales is demonstrated, which is correlated with certain geographic features of the areas from which the skulls were obtained.     

Variations of the chromosome number in the red fox (Vulpes vulpes)

The chromosome number in peripheral blood cells of five individuals of Vulpes vulpes (Red Fox) is shown to vary between 35 and 39. This variation is due to loss or gain of the smallest autosome, which it is suggested is heterochromatic and does not have any major influence on the phenotype. This species demonstrates variation in chromosome number both between and within individuals.