Nonecological speciation explained

When speciation is not driven by (or strongly correlated with) divergent natural selection, it can be said to be nonecological,^{[1] [2]} so as to distinguish it from the typical definition of ecological speciation: "It is useful to consider ecological speciation as its own form of species formation because it focuses on an explicit mechanism of speciation: namely divergent natural selection. There are numerous ways other than via divergent natural selection in which populations might become genetically differentiated and reproductively isolated."^[3] It is likely that many instances of nonecological speciation are allopatric, especially when the organisms in question are poor dispersers (e.g., land snails, salamanders), however sympatric nonecological speciation may also be possible, especially when accompanied by an "instant" (at least in evolutionary time) loss of reproductive compatibility, as when polyploidization happens.^[4] Other potential mechanisms for nonecological speciation include mutation-order speciation^[5] and changes in chirality in gastropods.^[6]

Nonecological speciation might not be accompanied by strong morphological differentiation, so might give rise to cryptic species, however there are some species that are difficult for humans to differentiate that are strongly differentiated with respect to their resource use, and so are likely a result of ecological speciation (e.g., host shifts in parasites or phytophagous insects).^{[7] [8]} When species recognition/sexual selection plays a strong role in maintaining species boundaries, the species generated by nonecological speciation might be straightforward for humans to differentiate, as in some odonates.^[9]

See also

• Nonadaptive radiation

References

1. Rundell. Rebecca J.. Price. Trevor D.. 2009-07-01. Adaptive radiation, nonadaptive radiation, ecological speciation and nonecological speciation. Trends in Ecology & Evolution. en. 24. 7. 394–399. 10.1016/j.tree.2009.02.007. 0169-5347. 19409647.
2. Czekanski-Moir. Jesse E.. Rundell. Rebecca J.. 2019-05-01. The Ecology of Nonecological Speciation and Nonadaptive Radiations. Trends in Ecology & Evolution. en. 34. 5. 400–415. 10.1016/j.tree.2019.01.012. 0169-5347. 30824193. 73494468 .
3. Book: Nosil, Patrik.. Ecological speciation. 2012. Oxford University Press. 978-0-19-162801-6. Oxford. 787851773.
4. Les. Donald H.. Peredo. Elena L.. King. Ursula M.. Benoit. Lori K.. Tippery. Nicholas P.. Ball. Cassandra J.. Shannon. Robynn K.. 2015-01-01. Through thick and thin: Cryptic sympatric speciation in the submersed genus Najas (Hydrocharitaceae). Molecular Phylogenetics and Evolution. en. 82. 15–30. 10.1016/j.ympev.2014.09.022. 25300454. 1055-7903.
5. Nosil. Patrik. Flaxman. Samuel M.. 2011-02-07. Conditions for mutation-order speciation. Proceedings of the Royal Society B: Biological Sciences. 278. 1704. 399–407. 10.1098/rspb.2010.1215. 3013408. 20702458.
6. Gittenberger. Edmund. Hamann. Thomas D.. Asami. Takahiro. 2012-04-20. Chiral Speciation in Terrestrial Pulmonate Snails. PLOS ONE. en. 7. 4. e34005. 10.1371/journal.pone.0034005. 1932-6203. 3332057. 22532825. 2012PLoSO...734005G. free.
7. Faucci. Anuschka. Toonen. Robert J. Hadfield. Michael G. 2007-01-07. Host shift and speciation in a coral-feeding nudibranch. Proceedings of the Royal Society B: Biological Sciences. 274. 1606. 111–119. 10.1098/rspb.2006.3685. 1679885. 17134995.
8. Lee. Y.. Lee. W.. Lee. S.. Kim. H.. February 2015. A cryptic species of Aphis gossypii (Hemiptera: Aphididae) complex revealed by genetic divergence and different host plant association. Bulletin of Entomological Research. en. 105. 1. 40–51. 10.1017/S0007485314000704. 25413997. 26358620. 0007-4853.
9. Wellenreuther . Maren . Maren Wellenreuther . Sánchez-Guillén . Rosa Ana . 2016 . Nonadaptive radiation in damselflies . Evolutionary Applications . en . 9 . 1 . 103–118 . 2016EvApp...9..103W . 10.1111/eva.12269 . 1752-4571 . 4780385 . 27087842.