Literature DB >> 12531306

Spatial and temporal analysis of second-generation anticoagulant rodenticide residues in polecats (Mustela putorius) from throughout their range in Britain, 1992-1999.

R F Shore1, J D S Birks, A Afsar, C L Wienburg, A C Kitchener.   

Abstract

Polecats (Mustela putorius) in Britain are currently expanding their range eastwards from Wales to reoccupy central and eastern areas of England. Second-generation anticoagulant rodenticides (SGARs), to which polecats are exposed by eating contaminated prey, are used more extensively in these central and eastern regions, leading to fears of increased exposure, and possible resultant mortality. We measured bromadiolone, difenacoum, flocoumafen and brodifacoum concentrations in the livers of 50 polecats from areas that included newly recolonised habitats and found that at least one SGAR was detected in the livers of 13 out of 37 (35.1%) male and 5 out of 13 (38.5%) female polecats. Difenacoum and bromadiolone were detected most frequently. We then combined these data with measurements on another 50 individuals from earlier studies to create a dataset for 100 polecats collected throughout the 1990s from across the whole of their current range. Using this dataset, we determined if there was any evidence that contamination in polecats had increased during the 1990s and whether animals from England were more contaminated than those from Wales, as might be expected given regional differences in the patterns of SGAR use. Overall, 31 of the 100 polecats analysed to date contained SGAR residues. The incidence was a little higher (40%) in animals that died between January and June and this probably better reflects the overall proportion of animals that are sub-lethally exposed. There was no statistically significant change during the 1990s in the proportion of polecats exposed to SGARs nor any evidence that greater use of SGARs in England resulted in more contamination of polecats. Contrary to expectation, the proportion of animals that contained difenacoum was marginally higher in Wales than elsewhere.

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Year:  2003        PMID: 12531306     DOI: 10.1016/s0269-7491(02)00297-x

Source DB:  PubMed          Journal:  Environ Pollut        ISSN: 0269-7491            Impact factor:   8.071


  6 in total

1.  Rodenticide exposure in wood mouse and house mouse populations on farms and potential secondary risk to predators.

Authors:  David G Tosh; Robbie A McDonald; Stuart Bearhop; Neville R Llewellyn; W Ian Montgomery; Richard F Shore
Journal:  Ecotoxicology       Date:  2012-03-24       Impact factor: 2.823

2.  Anticoagulant rodenticides in urban bobcats: exposure, risk factors and potential effects based on a 16-year study.

Authors:  L E K Serieys; T C Armenta; J G Moriarty; E E Boydston; L M Lyren; R H Poppenga; K R Crooks; R K Wayne; S P D Riley
Journal:  Ecotoxicology       Date:  2015-02-25       Impact factor: 2.823

3.  Monitoring agricultural rodenticide use and secondary exposure of raptors in Scotland.

Authors:  J Hughes; E Sharp; M J Taylor; L Melton; G Hartley
Journal:  Ecotoxicology       Date:  2013-04-18       Impact factor: 2.823

4.  Effects of Low-level Brodifacoum Exposure on the Feline Immune Response.

Authors:  Jennifer H Kopanke; Katherine E Horak; Esther Musselman; Craig A Miller; Kristine Bennett; Christine S Olver; Steven F Volker; Sue VandeWoude; Sarah N Bevins
Journal:  Sci Rep       Date:  2018-05-25       Impact factor: 4.379

5.  Relation between Intensity of Biocide Practice and Residues of Anticoagulant Rodenticides in Red Foxes (Vulpes vulpes).

Authors:  Anke Geduhn; Jens Jacob; Detlef Schenke; Barbara Keller; Sven Kleinschmidt; Alexandra Esther
Journal:  PLoS One       Date:  2015-09-29       Impact factor: 3.240

6.  Quantitative method for analysis of six anticoagulant rodenticides in faeces, applied in a case with repeated samples from a dog.

Authors:  Kristin Opdal Seljetun; Elin Eliassen; Ritva Karinen; Lars Moe; Vigdis Vindenes
Journal:  Acta Vet Scand       Date:  2018-01-17       Impact factor: 1.695

  6 in total

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