Reticulated adaptive radiation and phylogenomic diversity loss in the Hawaiian honeycreepers

The Hawaiian honeycreepers, one of the world’s most iconic adaptive radiations, are facing a human-mediated extinction crisis. More than 60 Hawaiian honeycreepers (Fringillidae: Carduelinae: Drepanidini) evolved from a single rosefinch-like ancestor that colonized the Hawaiian Islands. Only 17 Hawaiian honeycreeper taxa are known to be extant, of which only the common ‘amakihi ( Chlorodrepanis virens ) and ‘apapane ( Himatione sanguinea ) are classified as “Least Concern.” Using mitogenome, whole-genome, and hybridization-capture data, we present a comprehensive phylogeny of the historically known Hawaiian honeycreeper radiation. We also place two taxa known only from paleontological specimens ( Vangulifer neophasis and cf. Xestospiza conica ) in their phylogenomic context. We demonstrate that most Hawaiian honeycreeper lineages diversified in a “Big Bang” of adaptive radiation correlating with the formation of O‘ahu and that interspecies introgression likely played a role in this process. Using whole-genome data, we confirm putative interspecies admixture [N. A. S. Przelomska et al. , Biol. Lett. 21 , 20250265 (2025)] between the ‘ō‘ū ( Psittirostra psittacea ) and Lāna‘i hookbill ( Dysmorodrepanis munroi ) and document ongoing gene flow across the ‘amakihi species complex. Furthermore, we reject the synonymization of Vestiaria (‘i‘iwi) and Drepanis (Hawai‘i and black mamo). Instead, the mamo species form an extinct clade with no close extant relatives, demonstrating a greater loss of phylogenomic diversity than previously understood.

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Journal
Proceedings of the National Academy of Sciences
Published
2026-08-03
DOI
https://doi.org/10.1073/pnas.2536533123
Primary Topic
Genomics and Phylogenetic Studies
Type
article
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article

Reticulated adaptive radiation and phylogenomic diversity loss in the Hawaiian honeycreepers

Nancy Rotzel McInerney, Loren Cassin‐Sackett, Amberleigh E. Henschen, Madhvi X. Venkatraman et al.
Proceedings of the National Academy of Sciences
Genomics and Phylogenetic Studies
article

Reticulated adaptive radiation and phylogenomic diversity loss in the Hawaiian honeycreepers

Nancy Rotzel McInerney, Loren Cassin‐Sackett, Amberleigh E. Henschen, Madhvi X. Venkatraman, Natalia A. S. Przelomska, Nichelle M. VanTassel, Molly E. Hagemann, Heather R. L. Lerner, Helen F. James, Mirian T. N. Tsuchiya, Michael G. Campana, Anna M. Kearns, Eben H. Paxton, Margad-Erdene Ochirbat, Robert C. Fleischer, Taylor E. Callicrate
article en

Abstract

The Hawaiian honeycreepers, one of the world’s most iconic adaptive radiations, are facing a human-mediated extinction crisis. More than 60 Hawaiian honeycreepers (Fringillidae: Carduelinae: Drepanidini) evolved from a single rosefinch-like ancestor that colonized the Hawaiian Islands. Only 17 Hawaiian honeycreeper taxa are known to be extant, of which only the common ‘amakihi ( Chlorodrepanis virens ) and ‘apapane ( Himatione sanguinea ) are classified as “Least Concern.” Using mitogenome, whole-genome, and hybridization-capture data, we present a comprehensive phylogeny of the historically known Hawaiian honeycreeper radiation. We also place two taxa known only from paleontological specimens ( Vangulifer neophasis and cf. Xestospiza conica ) in their phylogenomic context. We demonstrate that most Hawaiian honeycreeper lineages diversified in a “Big Bang” of adaptive radiation correlating with the formation of O‘ahu and that interspecies introgression likely played a role in this process. Using whole-genome data, we confirm putative interspecies admixture [N. A. S. Przelomska et al. , Biol. Lett. 21 , 20250265 (2025)] between the ‘ō‘ū ( Psittirostra psittacea ) and Lāna‘i hookbill ( Dysmorodrepanis munroi ) and document ongoing gene flow across the ‘amakihi species complex. Furthermore, we reject the synonymization of Vestiaria (‘i‘iwi) and Drepanis (Hawai‘i and black mamo). Instead, the mamo species form an extinct clade with no close extant relatives, demonstrating a greater loss of phylogenomic diversity than previously understood.

Proceedings of the National Academy of SciencesVol. 123(32)
Smithsonian Institution (US), United States Geological Survey (US), Earlham College (US), South Carolina Department of Natural Resources (US), Bernice P. Bishop Museum (US), Eastern Illinois University (US), Royal Botanic Gardens, Kew (GB), Smithsonian Conservation Biology Institute (US), Pacific Science Center (US), NCCOS Hollings Marine Laboratory (US), National Museum of Natural History (BG), Australian National Wildlife Collection (AU), University of Portsmouth (GB), University of Louisiana at Lafayette (US)
National Science Foundation, U.S. Fish and Wildlife Service
Life below water
Openalex Percentile: Top 16%
Genomics and Phylogenetic Studies
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