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Habitat selection by vulnerable golden bandicoots in the arid zone
In 2010, vulnerable golden bandicoots (Isoodon auratus) were translocated from Barrow Island, Western Australia, to a mainland predator‐free enclosure on the Matuwa Indigenous Protected Area. Golden bandicoots were once widespread throughout a variety of arid and semiarid habitats of central and nor...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8328459/ https://www.ncbi.nlm.nih.gov/pubmed/34367603 http://dx.doi.org/10.1002/ece3.7875 |
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author | Lohr, Cheryl A. Nilsson, Kristen Sims, Colleen Dunlop, Judy Lohr, Michael T. |
author_facet | Lohr, Cheryl A. Nilsson, Kristen Sims, Colleen Dunlop, Judy Lohr, Michael T. |
author_sort | Lohr, Cheryl A. |
collection | PubMed |
description | In 2010, vulnerable golden bandicoots (Isoodon auratus) were translocated from Barrow Island, Western Australia, to a mainland predator‐free enclosure on the Matuwa Indigenous Protected Area. Golden bandicoots were once widespread throughout a variety of arid and semiarid habitats of central and northern Australia. Like many small‐to‐medium‐sized marsupials, the species has severely declined since colonization and has been reduced to only four remnant natural populations. Between 2010 and 2020, the reintroduced population of golden bandicoots on Matuwa was monitored via capture–mark–recapture data collection, which was used in spatially explicit capture–recapture analysis to monitor their abundance over time. In 2014, we used VHF transmitters to examine the home range and habitat selection of 20 golden bandicoots in the enclosure over a six‐week period. We used compositional analysis to compare the use of four habitat types. Golden bandicoot abundance in the enclosure slowly increased between 2010 and 2014 and has since plateaued at approximately one quarter of the density observed in the founding population on Barrow Island. The population may have plateaued because some bandicoots escape through the fence. Golden bandicoots used habitats dominated by scattered shrubland with spinifex grass more than expected given the habitat's availability. Nocturnal foraging range was influenced by sex and trapping location, whereas diurnal refuge habitat, which was typically under a spinifex hummock with minimal overstory vegetation, was consistent across sex and trapping location. Our work suggests that diurnal refuge habitat may be an important factor for the success of proposed translocations of golden bandicoots. |
format | Online Article Text |
id | pubmed-8328459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83284592021-08-06 Habitat selection by vulnerable golden bandicoots in the arid zone Lohr, Cheryl A. Nilsson, Kristen Sims, Colleen Dunlop, Judy Lohr, Michael T. Ecol Evol Original Research In 2010, vulnerable golden bandicoots (Isoodon auratus) were translocated from Barrow Island, Western Australia, to a mainland predator‐free enclosure on the Matuwa Indigenous Protected Area. Golden bandicoots were once widespread throughout a variety of arid and semiarid habitats of central and northern Australia. Like many small‐to‐medium‐sized marsupials, the species has severely declined since colonization and has been reduced to only four remnant natural populations. Between 2010 and 2020, the reintroduced population of golden bandicoots on Matuwa was monitored via capture–mark–recapture data collection, which was used in spatially explicit capture–recapture analysis to monitor their abundance over time. In 2014, we used VHF transmitters to examine the home range and habitat selection of 20 golden bandicoots in the enclosure over a six‐week period. We used compositional analysis to compare the use of four habitat types. Golden bandicoot abundance in the enclosure slowly increased between 2010 and 2014 and has since plateaued at approximately one quarter of the density observed in the founding population on Barrow Island. The population may have plateaued because some bandicoots escape through the fence. Golden bandicoots used habitats dominated by scattered shrubland with spinifex grass more than expected given the habitat's availability. Nocturnal foraging range was influenced by sex and trapping location, whereas diurnal refuge habitat, which was typically under a spinifex hummock with minimal overstory vegetation, was consistent across sex and trapping location. Our work suggests that diurnal refuge habitat may be an important factor for the success of proposed translocations of golden bandicoots. John Wiley and Sons Inc. 2021-07-08 /pmc/articles/PMC8328459/ /pubmed/34367603 http://dx.doi.org/10.1002/ece3.7875 Text en © 2021 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Lohr, Cheryl A. Nilsson, Kristen Sims, Colleen Dunlop, Judy Lohr, Michael T. Habitat selection by vulnerable golden bandicoots in the arid zone |
title | Habitat selection by vulnerable golden bandicoots in the arid zone |
title_full | Habitat selection by vulnerable golden bandicoots in the arid zone |
title_fullStr | Habitat selection by vulnerable golden bandicoots in the arid zone |
title_full_unstemmed | Habitat selection by vulnerable golden bandicoots in the arid zone |
title_short | Habitat selection by vulnerable golden bandicoots in the arid zone |
title_sort | habitat selection by vulnerable golden bandicoots in the arid zone |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8328459/ https://www.ncbi.nlm.nih.gov/pubmed/34367603 http://dx.doi.org/10.1002/ece3.7875 |
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