» Articles » PMID: 35831431

Using PVA and Captive Breeding to Balance Trade-offs in the Rescue of the Island Dibbler Onto a New Island Ark

Overview
Journal Sci Rep
Specialty Science
Date 2022 Jul 13
PMID 35831431
Authors
Affiliations
Soon will be listed here.
Abstract

In the face of the current global extinction crisis, it is critical we give conservation management strategies the best chance of success. Australia is not exempt from global trends with currently the world's greatest mammal extinction rate (~ 1 per 8 years). Many more are threatened including the dibbler (Parantechinus apicalis) whose remnant range has been restricted to Western Australia at just one mainland site and two small offshore islands-Whitlock Island (5 ha) and Boullanger Island (35 ha). Here, we used 14 microsatellite markers to quantify genetic variation in the remaining island populations from 2013 to 2018 and incorporated these data into population viability analysis (PVA) models, used to assess factors important to dibbler survival and to provide guidance for translocations. Remnant population genetic diversity was low (< 0.3), and populations were highly divergent from each other (pairwise Fs 0.29-0.52). Comparison of empirical data to an earlier study is consistent with recent declines in genetic diversity and models projected increasing extinction risk and declining genetic variation in the next century. Optimal translocation scenarios recommend 80 founders for new dibbler populations-provided by captive breeding-and determined the proportion of founders from parental populations to maximise genetic diversity and minimise harvesting impact. The goal of our approach is long-term survival of genetically diverse, self-sustaining populations and our methods are transferable. We consider mixing island with mainland dibblers to reinforce genetic variation.

Citing Articles

Diverged Populations Admixture Bolsters Genetic Diversity of a New Island Dibbler () Population, but Does Not Prevent Subsequent Loss of Genetic Variation.

Thavornkanlapachai R, Mills H, Ottewell K, Lambert C, Friend J, White D Evol Appl. 2025; 18(1):e70073.

PMID: 39845580 PMC: 11750805. DOI: 10.1111/eva.70073.


Airports for the genetic rescue of a former agricultural pest.

Buci M, Krajmerova D, Tam B, Kanuch P, Klinga P Sci Rep. 2024; 14(1):17540.

PMID: 39080479 PMC: 11289432. DOI: 10.1038/s41598-024-68679-y.


Population genomic diversity and structure in the golden bandicoot: a history of isolation, extirpation, and conservation.

Rick K, Byrne M, Cameron S, Cooper S, Dunlop J, Hill B Heredity (Edinb). 2023; 131(5-6):374-386.

PMID: 37806995 PMC: 10673901. DOI: 10.1038/s41437-023-00653-2.


: Multispecies Fauna Reconstruction Requires Thinking Outside the Box.

Cowen S, Sims C, Ottewell K, Knox F, Friend T, Mills H Animals (Basel). 2023; 13(17).

PMID: 37685026 PMC: 10486414. DOI: 10.3390/ani13172762.

References
1.
Foerster K, Delhey K, Johnsen A, Lifjeld J, Kempenaers B . Females increase offspring heterozygosity and fitness through extra-pair matings. Nature. 2003; 425(6959):714-7. DOI: 10.1038/nature01969. View

2.
Armbruster , Bradshaw , STEINER , Holzapfel . Evolutionary responses to environmental stress by the pitcher-plant mosquito, wyeomyia smithii. Heredity (Edinb). 2000; 83 (Pt 5):509-19. DOI: 10.1038/sj.hdy.6886040. View

3.
Kennington W, Hevroy T, Johnson M . Long-term genetic monitoring reveals contrasting changes in the genetic composition of newly established populations of the intertidal snail Bembicium vittatum. Mol Ecol. 2012; 21(14):3489-500. DOI: 10.1111/j.1365-294X.2012.05636.x. View

4.
Pujolar J, Maes G, Vancoillie C, Volckaert F . Growth rate correlates to individual heterozygosity in the European eel, Anguilla anguilla L. Evolution. 2005; 59(1):189-99. View

5.
Akesson M, Liberg O, Sand H, Wabakken P, Bensch S, Flagstad O . Genetic rescue in a severely inbred wolf population. Mol Ecol. 2016; 25(19):4745-56. PMC: 5054837. DOI: 10.1111/mec.13797. View