The coincidence of ecological opportunity with hybridization explains rapid adaptive radiation in Lake Mweru cichlid fishes
Joana I. Meier,
Rike B. Stelkens,
Domino A. Joyce,
Salome Mwaiko,
Numel Phiri,
Ulrich K. Schliewen,
Oliver M. Selz,
Catherine E. Wagner,
Cyprian Katongo and
Ole Seehausen ()
Additional contact information
Joana I. Meier: University of Bern, Baltzerstr. 6
Rike B. Stelkens: University of Bern, Baltzerstr. 6
Domino A. Joyce: University of Hull
Salome Mwaiko: University of Bern, Baltzerstr. 6
Numel Phiri: University of Zambia
Ulrich K. Schliewen: SNSB-Bavarian State Collection of Zoology, Münchhausenstrasse 21
Oliver M. Selz: University of Bern, Baltzerstr. 6
Catherine E. Wagner: University of Bern, Baltzerstr. 6
Cyprian Katongo: University of Zambia
Ole Seehausen: University of Bern, Baltzerstr. 6
Nature Communications, 2019, vol. 10, issue 1, 1-11
Abstract:
Abstract The process of adaptive radiation was classically hypothesized to require isolation of a lineage from its source (no gene flow) and from related species (no competition). Alternatively, hybridization between species may generate genetic variation that facilitates adaptive radiation. Here we study haplochromine cichlid assemblages in two African Great Lakes to test these hypotheses. Greater biotic isolation (fewer lineages) predicts fewer constraints by competition and hence more ecological opportunity in Lake Bangweulu, whereas opportunity for hybridization predicts increased genetic potential in Lake Mweru. In Lake Bangweulu, we find no evidence for hybridization but also no adaptive radiation. We show that the Bangweulu lineages also colonized Lake Mweru, where they hybridized with Congolese lineages and then underwent multiple adaptive radiations that are strikingly complementary in ecology and morphology. Our data suggest that the presence of several related lineages does not necessarily prevent adaptive radiation, although it constrains the trajectories of morphological diversification. It might instead facilitate adaptive radiation when hybridization generates genetic variation, without which radiation may start much later, progress more slowly or never occur.
Date: 2019
References: Add references at CitEc
Citations: View citations in EconPapers (2)
Downloads: (external link)
https://www.nature.com/articles/s41467-019-13278-z Abstract (text/html)
Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.
Export reference: BibTeX
RIS (EndNote, ProCite, RefMan)
HTML/Text
Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-13278-z
Ordering information: This journal article can be ordered from
https://www.nature.com/ncomms/
DOI: 10.1038/s41467-019-13278-z
Access Statistics for this article
Nature Communications is currently edited by Nathalie Le Bot, Enda Bergin and Fiona Gillespie
More articles in Nature Communications from Nature
Bibliographic data for series maintained by Sonal Shukla () and Springer Nature Abstracting and Indexing ().