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Acute oral toxicity of zinc phosphide: an assessment for wild house mice (Mus musculus)

Irregular plagues of house mice, Mus musculus, incur major economic impacts on agricultural production in Australia. The efficacy of zinc phosphide (ZnP), the only registered broadacre control agent for mice, is reported as increasingly variable. Have mice become less sensitive over time or are they...

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Autores principales: HINDS, Lyn A., HENRY, Steve, VAN DE WEYER, Nikki, ROBINSON, Freya, RUSCOE, Wendy A., BROWN, Peter R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10084325/
https://www.ncbi.nlm.nih.gov/pubmed/35651323
http://dx.doi.org/10.1111/1749-4877.12666
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author HINDS, Lyn A.
HENRY, Steve
VAN DE WEYER, Nikki
ROBINSON, Freya
RUSCOE, Wendy A.
BROWN, Peter R.
author_facet HINDS, Lyn A.
HENRY, Steve
VAN DE WEYER, Nikki
ROBINSON, Freya
RUSCOE, Wendy A.
BROWN, Peter R.
author_sort HINDS, Lyn A.
collection PubMed
description Irregular plagues of house mice, Mus musculus, incur major economic impacts on agricultural production in Australia. The efficacy of zinc phosphide (ZnP), the only registered broadacre control agent for mice, is reported as increasingly variable. Have mice become less sensitive over time or are they taking a sub‐lethal dose and developing aversion? In this laboratory study, the sensitivity of mice (wild caught; outbred laboratory strain) was assessed using oral gavage of a range of ZnP concentrations. The estimated LD(50) values (72–79 mg ZnP/kg body weight) were similar for each mouse group but are significantly higher than previously reported. The willingness of mice to consume ZnP‐coated grains was determined. ZnP‐coated grains (50 g ZnP/kg grain) presented in the absence of alternative food were consumed and 94% of wild mice died. Mice provided with alternative food and ZnP‐coated wheat grains (either 25 or 50 g ZnP/kg grain) consumed toxic and non‐toxic grains, and mortality was lower (33–55%). If a sublethal amount of ZnP‐coated grain was consumed, aversion occurred, mostly when alternative food was present. The sensitivity of wild house mice to ZnP in Australia is significantly lower than previously assumed. Under laboratory conditions, ZnP‐coated grains coated with a new higher dose (50 g ZnP/kg grain) were readily consumed. Consumption of toxic grain occurred when alternative food was available but was decreased. Our unambiguous findings for house mice indicate a re‐assessment of the ZnP loading for baits used for control of many rodents around the world may be warranted.
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spelling pubmed-100843252023-04-11 Acute oral toxicity of zinc phosphide: an assessment for wild house mice (Mus musculus) HINDS, Lyn A. HENRY, Steve VAN DE WEYER, Nikki ROBINSON, Freya RUSCOE, Wendy A. BROWN, Peter R. Integr Zool Special subsection: Physiological ecology Irregular plagues of house mice, Mus musculus, incur major economic impacts on agricultural production in Australia. The efficacy of zinc phosphide (ZnP), the only registered broadacre control agent for mice, is reported as increasingly variable. Have mice become less sensitive over time or are they taking a sub‐lethal dose and developing aversion? In this laboratory study, the sensitivity of mice (wild caught; outbred laboratory strain) was assessed using oral gavage of a range of ZnP concentrations. The estimated LD(50) values (72–79 mg ZnP/kg body weight) were similar for each mouse group but are significantly higher than previously reported. The willingness of mice to consume ZnP‐coated grains was determined. ZnP‐coated grains (50 g ZnP/kg grain) presented in the absence of alternative food were consumed and 94% of wild mice died. Mice provided with alternative food and ZnP‐coated wheat grains (either 25 or 50 g ZnP/kg grain) consumed toxic and non‐toxic grains, and mortality was lower (33–55%). If a sublethal amount of ZnP‐coated grain was consumed, aversion occurred, mostly when alternative food was present. The sensitivity of wild house mice to ZnP in Australia is significantly lower than previously assumed. Under laboratory conditions, ZnP‐coated grains coated with a new higher dose (50 g ZnP/kg grain) were readily consumed. Consumption of toxic grain occurred when alternative food was available but was decreased. Our unambiguous findings for house mice indicate a re‐assessment of the ZnP loading for baits used for control of many rodents around the world may be warranted. John Wiley and Sons Inc. 2022-06-20 2023-01 /pmc/articles/PMC10084325/ /pubmed/35651323 http://dx.doi.org/10.1111/1749-4877.12666 Text en © 2022 CSIRO Health and Biosecurity. Integrative Zoology published by International Society of Zoological Sciences, Institute of Zoology/Chinese Academy of Sciences and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Special subsection: Physiological ecology
HINDS, Lyn A.
HENRY, Steve
VAN DE WEYER, Nikki
ROBINSON, Freya
RUSCOE, Wendy A.
BROWN, Peter R.
Acute oral toxicity of zinc phosphide: an assessment for wild house mice (Mus musculus)
title Acute oral toxicity of zinc phosphide: an assessment for wild house mice (Mus musculus)
title_full Acute oral toxicity of zinc phosphide: an assessment for wild house mice (Mus musculus)
title_fullStr Acute oral toxicity of zinc phosphide: an assessment for wild house mice (Mus musculus)
title_full_unstemmed Acute oral toxicity of zinc phosphide: an assessment for wild house mice (Mus musculus)
title_short Acute oral toxicity of zinc phosphide: an assessment for wild house mice (Mus musculus)
title_sort acute oral toxicity of zinc phosphide: an assessment for wild house mice (mus musculus)
topic Special subsection: Physiological ecology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10084325/
https://www.ncbi.nlm.nih.gov/pubmed/35651323
http://dx.doi.org/10.1111/1749-4877.12666
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