Rhodamine B as a systemic hair marker for assessment of bait acceptance by stoats (Mustela erminea)

Abstract

Rhodamine B (RB) is a dye that becomes incorporated into the structure of growing hair of animals that ingest it, appearing as an orange‐red fluorescent band detectable under a fluorescent‐light microscope. This marker was evaluated as a means of assessing bait acceptance by stoats (Mustela erminea L.). Eleven wild‐caught captive stoats were each fed a broken hen egg injected with 25 mg of RB on two occasions, 5 weeks apart. This was equivalent to 62–108 mg kg^–1, depending upon stoat weight, on each occasion. At least three facial whiskers were collected from each dosed stoat on each of two sampling dates (giving a total of at least six whiskers from each stoat). The sampling dates varied from 1 to 17 weeks after first dosing. Whiskers were also collected from one of the dosed stoats that died of other causes 19 weeks after first dosing, and from four stoats not dosed with RB. All 11 of the stoats fed RB had at least one fluorescent band in at least one of the sampled whiskers. None of the four stoats not fed RB had fluorescent bands in their whiskers. The marking persisted in all dosed stoats for at least 6 weeks, and in one dosed stoat for at least 19 weeks after dosing. However, only 56% of the 91 whiskers inspected from the dosed stoats had fluorescent bands, and only 9% of the whiskers had two fluorescent bands, representing the two doses of RB. The distance between the two fluorescent bands indicated a mean whisker growth of 0.6 mm day^‐1. The distance from the base of the whiskers to the base of the fluorescent bands was broadly related to the time after ingestion of bait containing RB. However, the variation was too great for distance along the whisker to be reliably used as a quantitative measure of time after bait ingestion. The technique can be used to assess bait acceptance in the field provided all stoats are sampled within c. 4–6 weeks of baiting, and at least 6–9 whiskers are sampled from each stoat.     

Field experiments on the trapping of stoats (Mustela erminea)

Abstract

Steel Fenn traps spaced at 100 m, 200 m, 400 m, and 800 m intervals (total 88 traps) were set in the Eglinton and Hollyford valleys, Fiordland, New Zealand, for 14 days a month from November 1974 to March 1976. A total of 173 stoats were caught, mostly in the two summers. The number of stoats caught and the proportion of females did not change with trap spacing, but both were higher than in an earlier, informal trapping campaign in the same area (20 traps at 2.1 km average interval; 124 stoats caught). The capture rate on the experimental lines declined from 1.07 stoats per 100 trap-nights at the beginning of the average 14-day session to 0.42 at the end, a reduction of 60%. Immigration between trapping sessions probably occurred in all months, but was most marked in summer. The usefulness of the data for the formulation of management policies concerning stoats in the National Parks of New Zealand will be discussed, along with other relevant information, elsewhere.     

The potential for biological control of stoats (Mustela erminea)

Abstract

Accelerating the mortality of stoats (Mustela erminea) using biological agents, or reducing their fertility using chemosterilants or biological agents, are increasingly seen as more sustainable and more humane than trapping and poisoning. Obligate delayed implantation in fertilised female stoats of all ages allows 10–11 months for an applied biological agent or chemosterilant to interfere with gestation. Two chemosterilants (cabergoline and mifepristone) disrupt pregnancy in some species and may be effective on stoats, although they are not species‐specific and are probably more expensive than poisoning. For the longer term, more recent fertility control research has explored potentially more species‐specific options for other species based on inducing an immune response to an animal's own reproductive hormones, gametes, or products from embryos. Conception will be difficult to disrupt in stoats because females are sexually mature and are mated in the nest during a short period before they are weaned. A large research effort will be required to determine which of the immunosterilants being developed could be suitable candidates for stoat control. There are fewer options apparent for using biological agents to increase stoat mortality, although species‐specific strains of canine distemper virus may be effective against stoats.

The greatest impediment to controlling stoat fertility will be effective delivery of sterilants. For the foreseeable future, it will probably be necessary to rely on baits, but they are unlikely to put all target stoats at risk, and will be incapable of delivery over larger scales than at present.

Before undertaking expensive field trials and development of anti‐fertility and biological agents, the effects of putative compensatory changes in demographics that may be associated with changes in stoat density should be modelled to see if the sterilisation and mortality rates that are required to achieve a given level of population control are realistic targets. Also, population control should be defined in terms of accrued benefit for wildlife by establishing the relationships between stoat densities and the viability of prey populations.

Biological control of fertility or mortality may never be suitable as stand‐alone control options for stoats, particularly when some native fauna survive only if stoats are reduced to very low densities. Biological control may have greater potential when integrated with conventional control.     

Scats and den contents as indicators of the diet of stoats (Mustela erminea) in the Tasman Valley,South Canterbury,New Zealand

Stoats are significant predators of native fauna in New Zealand. They occur in many habitat types and consume a wide range of prey. The diet of stoats in the Tasman River, South Canterbury, was studied by analysis of scats and den contents. Analysis of 206 scats showed that stoats ate mainly lagomorphs, birds and invertebrates. Minor components included mice, lizards, fish and hedgehogs. Stoats ate more birds in spring than in autumn, and female stoats ate more invertebrates than did males. The contents of 219 dens collected in the same area at the same time provided further information. Birds and lagomorphs occurred at high frequency in dens, and other components were minor. Remains in dens were larger than in scats and allowed identification of many more prey items to species level. Den contents revealed a potentially substantial impact of stoats on threatened shorebirds locally; this impact was not detected by analysis of scats.     

Field trials of slow‐release synthetic lures for stoats (Mustela erminea) and ferrets (M. furo)

Abstract

Experimental field trials were used to compare the attractiveness to stoats (Mustela erminea) and ferrets (M. furo) of traps set with either a synthetic scent lure or with fresh food bait. One lure, containing 2‐n‐propylthietane, effectively attracted as many ferrets as did rabbit meat bait. Fewer stoats were caught with this lure than with egg bait. Made up in a slow‐release formulation in “plastic rope”, the lure remained attractive to ferrets for at least 2 weeks under sunny field conditions. Traps containing a second lure, 3‐n‐propyl‐l,2‐dithiolane, were less successful at catching both mustelid species than those containing fresh food baits. The scent lures were not attractive to non‐target species, but neither did they deter some species.     

A review of potential techniques for identifying individual stoats (Mustela erminea) visiting control or monitoring stations

Abstract

We review ways of individually identifying stoats (Mustela erminea) and similar small mammals from visits to bait stations or to monitoring devices in the field. Tracking devices are the cheapest and most practical method currently available of measuring the presence of a particular species, but there has been little research on the recognition of individuals. Elongation of tracking tunnels, or using sooty plates rather than ink to record prints, may improve detectability of individual markings. Recording visits to bait stations or tracking tunnels from DNA sequencing of hair or skin samples is likely to be prohibitively expensive for many monitoring programmes. Identification of stoats visiting bait stations or tracking tunnels using electronic devices has great potential, but these techniques are impracticably expensive because stoats move over such large areas that individual receivers and data loggers would be needed for each bait station. Chemical bait markers such as rhodamine B may be the most suitable method for identifying which animals have used a particular bait station.     

Captive husbandry of stoats Mustela erminea

Abstract

Captive stoats are essential for testing technological developments for pest control in New Zealand. We have reviewed husbandry practices and experiences of keeping stoats in captivity for a range of purposes. Stoats can be kept individually outside and subjected to normal regimes of light and temperature if sufficient bedding and shelter is provided. They appear to survive and breed best when fed on freshly killed rodents. Live prey is desirable though will rarely be permissible due to regulatory constraints. Breeding in captivity has been problematic in most cases, and although in a few instances wild‐caught females carrying embryos in delay have given birth, this is a rare event. Procedures taken to minimise stress in captivity may reduce the loss rate of blastocysts due to resorption and facilitate rapid expansion of captive colonies.     

Identification of a tyrosinase (TYR) exon 4 deletion in albino ferrets (Mustela putorius furo)

Albinism is due to a lack of pigmentation in hair, skin and eye, and has been shown to occur in several animal species. Mutations of the tyrosinase (TYR) gene account for albinism in domestic cats, rabbits, cattle, mice and rats. In this study, we demonstrate that a TYR mutation accounts for albinism in the ferret (Mustela putorius furo). The coding sequence of the five exons of TYR was determined in genomic DNA from wild-type pigmented 'sable' coloured and albino ferrets. It was not possible to amplify TYR exon 4 in albino ferrets originating from different breeds. The deletion of exon 4 in albino ferrets was confirmed by Southern blot hybridization of genomic DNA from albino and pigmented ferrets. This is the first report of a deletion of a TYR exon in a non-human mammal.     

The biology of the stoat (Mustela erminea) in the National Parks of New Zealand IV. Reproduction

Abstract

The gonads of 528 female and 821 male stoats were examined. The weights of ovaries and testes in adults peaked simultaneously in October, the season of births and of post-partum oestrus. Of 73 females, 78% had even numbers of nipples, mostly 8 or 10. The mean number of embryos in 13 pregnancies was 8.8 (6–13), and embryo weights ranged from 0.005 g to 2.9 g. Of 11 pregnant females, 8 contained fewer embryos than corpora lutea, and there was evidence of transuterine migration of blastocysts in 6. All but 2 of 451 females caught in December–July inclusive carried corpora lutea of delay. Few adult and no young females were found in oestrus in September–October, though adult males were fertile from August to February (no first-year males were fertile). There was some evidence that the breeding season started later at more southerly latitudes in both males and females. The mean number of corpora lutea per female was 9.7 (n = 439), and there was a significant inverse correlation between counts for the 2 ovaries of one individual. There was generally no significant variation in fecundity of females with age, body weight, or year. Of 11 females which were considered to have lost their litters, 10 were collected in beech (Nothofagus) forests. Four females and 9 males had abnormal gonads; the most severe abnormality was an ovarian teratoma of unknown pathology.     

The biology of the stoat (Mustela erminea) in the National Parks of New Zealand VI. Infestation with Skrjabingylus nasicola

Abstract

The natural distribution of the parasite Skrjabingylus nasicola was surveyed in 1492 stoats from New Zealand’s National Parks. Infestation was rare in the young, so distribution was expressed as frequency of occurrence of skulls containing nematodes in samples of stoats more than 6 months old. Conservative estimates of incidence ranged from 0 to 37% in 27 local subsamples with at least 6 adults and subadults (mean 10%, n = 1005), sometimes varying substantially across short distances. Incidence was highest in beech forest and scrub/grassland habitats with annual rainfall less than 1600 mm. Subadult males (6–10 months old) were infested as frequently as adult males (older than 10 months), and there was no difference in incidence between the sexes. Worms recovered from 97 infested stoats occurred equally often in either side of the skull; were more often large (i.e., probably female) at all intensities of infestation; and numbered 1–73 per infested stoat (mean 12.9 in females, 14.2 in males; difference not significant). There was no evidence that infested stoats were smaller or lighter than uninfested onces.     

Evaluation of iophenoxic acid and rhodamine B for marking feral ferrets (Mustela furo)

Abstract

The blood marker iophenoxic acid, and the fluorescent dye rhodamine B, were evaluated as means of assessing bait consumption in the ferret, Mustela furo. Iophenoxic acid was elevated above baseline concentrations for a minimum of 28 days after dosing, indicating that it is a suitable medium‐term marker. Rhodamine B marked ferrets for a maximum of 7 days, and would therefore have limited operational use with feral ferrets. Iophenoxic acid was used in a field trial to assess the effectiveness of a newly developed baiting strategy for control of wild ferrets. All 21 ferrets captured after field baiting with iophenoxic acid had elevated levels of serum iodine, indicating that the newly developed baiting strategy is highly effective for marking ferrets.     

Responses of stoats to scent lures in tracking tunnels

Abstract

Scent lures made from the anal sac secretions of stoats (Mustela ermined) in a long‐life formulation increased the number of visits by stoats to footprint tracking tunnels set near the shoreline of Lake Waikaremoana. Lures derived from female stoats received a similar number of visits to those derived from males. Blank lures with no active ingredient did not attract stoats. Most of the lures remained intact and active for about seven weeks in summer. Rodents were unaffected by the lures, being neither repelled by the scent of stoats, nor attracted to the edible casein‐based carrier compound. Our results suggest that scent lures could be useful for indexing stoat populations. Trials are needed to compare the effectiveness of lures and bait, and to determine seasonal changes in lure attractiveness. Problems of supply of the active ingredients will need to be overcome.     

Movements and home range of ferrets (Mustela furo) at Pukepuke Lagoon,New Zealand

Abstract

Ferrets at Pukepuke Lagoon were live-trapped during the periods November 1970 to August 1973 and January 1976 to July 1977. Although the sex ratio of the 75 trapped ferrets was equal, there was a strong bias towards male captures in the earlier period (58.4%) and towards female captures in the later period (68.7%). Habitat modification and changes in the trapping programme for the later period probably resulted in the increased abundance and capture rate of females. Between consecutive captures 58.2% of male movements exceeded 250 m, as against on1y 39.7% of female movements; the mean distance between consecutive captures was 435 m for males and 285 m for females. Mean monthly movements varied from 700 m in January to 315 m in June for males, and from 360 m in March to 150 m in September for females. Juveniles of both sexes moved similar, intermediate distances. Dispersing juveniles were trapped from January until April; males tended to appear in traps earlier in the year than females. Only 4 of 14 juvenile males setNed as residents, hut 15 of 28 juvenile females did so. Male and female home ranges overlapped extensively, but within each sex individual ranges were usually separate. Resident males maintained a well defined spacing pattern, adjusting their boundaries if a juvenile settled or a neighbouring range became vacant. In 1976 six females had overlapping ranges in an area of albundant food. Female ranges (12.4 ha) were on average smaller than male ranges (31.3 ha); home ranges of both sexes were smaller during the breeding season (August-February) than at other times.     

Trapping tunnel design incorporating behavioural preferences of stoats

Abstract

Stoats (Mustela erminea) are introduced pests in New Zealand, and there is an urgent need for effective trapping systems that kill the animal in a humane manner. A treadle trap was designed, the Dominus trap, that utilised an earlier‐proven humane killing system enhanced by the addition of a treadle plate trigger. This system enabled the trap to be classified as a Class A trap under the National Animal Welfare Advisory Committee (NAWAC) guidelines for animal kill traps, by successfully rendering 10/10 animals unconscious within 30 s. The Dominus trap mimics a tunnel, which by its very shape entices the animal to enter, but weighs only 600 g. Atrial at Flea Bay, on Banks Peninsula, used 35 Dominus traps placed alternately between 35 Fenn Mk VI traps set over 3150 trap nights (TN). The trial was conducted from March to May 2007 and was repeated for a further 7740 trap nights from January to March 2008, using 20 Dominus traps. The Dominus trap caught stoats consistently at the rate of 0.22 stoats/100 TN in both years, compared with 0 and 0.14/100 TN in Fenn traps, so potentially provides a humane alternative to the Fenn.     

The effects of mice on stoats in southern beech forests

Introduced stoats (Mustela erminea) are important invasive predators in southern beech (Nothofagus sp.) forests in New Zealand. In these forests, one of their primary prey species – introduced house mice (Mus musculus), fluctuate dramatically between years, driven by the irregular heavy seed‐fall (masting) of the beech trees. We examined the effects of mice on stoats in this system by comparing the weights, age structure and population densities of stoats caught on two large islands in Fiordland, New Zealand – one that has mice (Resolution Island) and one that does not (Secretary Island). On Resolution Island, the stoat population showed a history of recruitment spikes and troughs linked to beech masting, whereas the Secretary Island population had more constant recruitment, indicating that rodents are probably the primary cause for the ‘boom and bust’ population cycle of stoats in beech forests. Resolutions Island stoats were 10% heavier on average than Secretary Island stoats, supporting the hypothesis that the availability of larger prey (mice verses wētā) leads to larger stoats. Beech masting years on this island were also correlated with a higher weight for stoats born in the year of the masting event. The detailed demographic information on the stoat populations of these two islands supports previously suggested interactions among mice, stoats and beech masting. These interactions may have important consequences for the endemic species that interact with fluctuating populations of mice and stoats.     

The biology of the stoat (Mustela erminea) in the National Parks of New Zealand III. Morphometric variation in relation to growth,geographical distribution,and colonisation

Abstract

A total of 1599 stoats were collected from 14 study areas (including all 10 National Parks) from 1972 to 1976. Samples were larger in summer, and contained more females. Young stoats are born in September-October, and females reach adult weight by the following March, though males not until after August. There was significant geographic variation in the body size of adult stoats sampled: males from lowland podocarp/broadleaved forests averaged 3% smaller than males from upland beech forests in skull length, and 4% smaller in head-and-body length. This pattern was repeated, less clearly, in females and in young (approximately 2–5 months old). In contrast with stoats in Britain, assumed to be still the same size as the colonising stock introduced into New Zealand in 1884 and subsequently, males from lowland podocarp forests were unchanged or possibly smaller, and males from upland beech forests were larger; females were larger in all habitats. In males, the extent of geographic variation is almost as great in New Zealand as in the whole of continental Europe. Possible explanations of this pattern are discussed.