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Population genetics and phylogeography of sea turtles
Open accessAbstract
The seven species of sea turtles occupy a diversity of niches, and have a history tracing back over 100 million years, yet all share basic life‐history features, including exceptional navigation skills and periodic migrations from feeding to breeding habitats. Here, we review the biogeographic, behavioural, and ecological factors that shape the distribution of genetic diversity in sea turtles. Natal homing, wherein turtles return to their region of origin for mating and nesting, has been demonstrated with mtDNA sequences. These maternally inherited markers show strong population structure among nesting colonies while nuclear loci reveal a contrasting pattern of male‐mediated gene flow, a phenomenon termed ‘complex population structure’. Mixed‐stock analyses indicate that multiple nesting colonies can contribute to feeding aggregates, such that exploitation of turtles in these habitats can reduce breeding populations across the region. The mtDNA data also demonstrate migrations across entire ocean basins, some of the longest movements of marine vertebrates. Multiple paternity occurs at reported rates of 0–100%, and can vary by as much as 9–100% within species. Hybridization in almost every combination among members of the Cheloniidae has been documented but the frequency and ultimate ramifications of hybridization are not clear. The global phylogeography of sea turtles reveals a gradient based on habitat preference and thermal regime. The cold‐tolerant leatherback turtle (Dermochelys coriacea) shows no evolutionary partitions between Indo‐Pacific and Atlantic populations, while the tropical green (Chelonia mydas), hawksbill (Eretmochelys imbricata), and ridleys (Lepidochelys olivacea vs.L. kempi) have ancient separations between oceans. Ridleys and loggerhead (Caretta caretta) also show more recent colonization between ocean basins, probably mediated by warm‐water gyres that occasionally traverse the frigid upwelling zone in southern Africa. These rare events may be sufficient to prevent allopatric speciation under contemporary geographic and climatic conditions. Genetic studies have advanced our understanding of marine turtle biology and evolution, but significant gaps persist and provide challenges for the next generation of sea turtle geneticists.
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Body size, metabolic rate, generation time, and the molecular clock.
Martin, A. P., & Palumbi, S. R. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.9.4087 · Cited by 1,239 · cited 1×
“These demonstrated low genetic diversity, a theme that would recur in subsequent studies of mitochondrial DNA (mtDNA) and nuclear DNA (nDNA), possibly because of low metabolic rate and long generation time (Avise et al. 1992; Karl et al. 1992; Martin & Palumbi 1993).”
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Cited by
Mitochondrial DNA under siege in avian phylogeography
ZINK, R. M., & BARROWCLOUGH, G. F. (2008) · Molecular Ecology · doi:10.1111/j.1365-294x.2008.03737.x · Cited by 916
Wallace, B. P., DiMatteo, A. D., Hurley, B. J., Finkbeiner, E. M., Bolten, A. B., Chaloupka, M. Y., Hutchinson, B. J., Abreu-Grobois, F. A., Amorocho, D., Bjorndal, K. A., et al. (2010) · PLoS ONE · doi:10.1371/journal.pone.0015465 · Cited by 685
Self-citationMigration: The Biology of Life on the Move
Dingle, H. (2014) · doi:10.1093/acprof:oso/9780199640386.001.0001 · Cited by 455
Comparative phylogeography of the ocean planet
Bowen, B. W., Gaither, M. R., DiBattista, J. D., Iacchei, M., Andrews, K. R., Grant, W. S., Toonen, R. J., & Briggs, J. C. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1602404113 · Cited by 285
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Metadata
- Authors
- BOWEN, B. W., & KARL, S. A.
- Venue
- Molecular Ecology
- Publisher
- Wiley
- Published
- 2007-10-17
- Volume
- 16
- Issue
- 23
- Pages
- 4886-4907
- ISSN
- 0962-1083 (ISSN-L)
- 1365-294X
- OpenAlex
- W2014380564
- Cited by
- 505
- References
- 1
- FWCI
- 15.06
- Type
- journal article
- Language
- en
- Open access
- green
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