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Genetic structure along an elevational gradient in Hawaiian honeycreepers reveals contrasting evolutionary responses to avian malaria

BACKGROUND: The Hawaiian honeycreepers (Drepanidinae) are one of the best-known examples of an adaptive radiation, but their persistence today is threatened by the introduction of exotic pathogens and their vector, the mosquito Culex quinquefasciatus. Historically, species such as the amakihi (Hemig...

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Autores principales: Eggert, Lori S, Terwilliger, Lauren A, Woodworth, Bethany L, Hart, Patrick J, Palmer, Danielle, Fleischer, Robert C
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2613920/
https://www.ncbi.nlm.nih.gov/pubmed/19014596
http://dx.doi.org/10.1186/1471-2148-8-315
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author Eggert, Lori S
Terwilliger, Lauren A
Woodworth, Bethany L
Hart, Patrick J
Palmer, Danielle
Fleischer, Robert C
author_facet Eggert, Lori S
Terwilliger, Lauren A
Woodworth, Bethany L
Hart, Patrick J
Palmer, Danielle
Fleischer, Robert C
author_sort Eggert, Lori S
collection PubMed
description BACKGROUND: The Hawaiian honeycreepers (Drepanidinae) are one of the best-known examples of an adaptive radiation, but their persistence today is threatened by the introduction of exotic pathogens and their vector, the mosquito Culex quinquefasciatus. Historically, species such as the amakihi (Hemignathus virens), the apapane (Himatione sanguinea), and the iiwi (Vestiaria coccinea) were found from the coastal lowlands to the high elevation forests, but by the late 1800's they had become extremely rare in habitats below 900 m. Recently, however, populations of amakihi and apapane have been observed in low elevation habitats. We used twelve polymorphic microsatellite loci to investigate patterns of genetic structure, and to infer responses of these species to introduced avian malaria along an elevational gradient on the eastern flanks of Mauna Loa and Kilauea volcanoes on the island of Hawaii. RESULTS: Our results indicate that amakihi have genetically distinct, spatially structured populations that correspond with altitude. We detected very few apapane and no iiwi in low-elevation habitats, and genetic results reveal only minimal differentiation between populations at different altitudes in either of these species. CONCLUSION: Our results suggest that amakihi populations in low elevation habitats have not been recolonized by individuals from mid or high elevation refuges. After generations of strong selection for pathogen resistance, these populations have rebounded and amakihi have become common in regions in which they were previously rare or absent.
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spelling pubmed-26139202009-01-06 Genetic structure along an elevational gradient in Hawaiian honeycreepers reveals contrasting evolutionary responses to avian malaria Eggert, Lori S Terwilliger, Lauren A Woodworth, Bethany L Hart, Patrick J Palmer, Danielle Fleischer, Robert C BMC Evol Biol Research Article BACKGROUND: The Hawaiian honeycreepers (Drepanidinae) are one of the best-known examples of an adaptive radiation, but their persistence today is threatened by the introduction of exotic pathogens and their vector, the mosquito Culex quinquefasciatus. Historically, species such as the amakihi (Hemignathus virens), the apapane (Himatione sanguinea), and the iiwi (Vestiaria coccinea) were found from the coastal lowlands to the high elevation forests, but by the late 1800's they had become extremely rare in habitats below 900 m. Recently, however, populations of amakihi and apapane have been observed in low elevation habitats. We used twelve polymorphic microsatellite loci to investigate patterns of genetic structure, and to infer responses of these species to introduced avian malaria along an elevational gradient on the eastern flanks of Mauna Loa and Kilauea volcanoes on the island of Hawaii. RESULTS: Our results indicate that amakihi have genetically distinct, spatially structured populations that correspond with altitude. We detected very few apapane and no iiwi in low-elevation habitats, and genetic results reveal only minimal differentiation between populations at different altitudes in either of these species. CONCLUSION: Our results suggest that amakihi populations in low elevation habitats have not been recolonized by individuals from mid or high elevation refuges. After generations of strong selection for pathogen resistance, these populations have rebounded and amakihi have become common in regions in which they were previously rare or absent. BioMed Central 2008-11-14 /pmc/articles/PMC2613920/ /pubmed/19014596 http://dx.doi.org/10.1186/1471-2148-8-315 Text en Copyright ©2008 Eggert et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Eggert, Lori S
Terwilliger, Lauren A
Woodworth, Bethany L
Hart, Patrick J
Palmer, Danielle
Fleischer, Robert C
Genetic structure along an elevational gradient in Hawaiian honeycreepers reveals contrasting evolutionary responses to avian malaria
title Genetic structure along an elevational gradient in Hawaiian honeycreepers reveals contrasting evolutionary responses to avian malaria
title_full Genetic structure along an elevational gradient in Hawaiian honeycreepers reveals contrasting evolutionary responses to avian malaria
title_fullStr Genetic structure along an elevational gradient in Hawaiian honeycreepers reveals contrasting evolutionary responses to avian malaria
title_full_unstemmed Genetic structure along an elevational gradient in Hawaiian honeycreepers reveals contrasting evolutionary responses to avian malaria
title_short Genetic structure along an elevational gradient in Hawaiian honeycreepers reveals contrasting evolutionary responses to avian malaria
title_sort genetic structure along an elevational gradient in hawaiian honeycreepers reveals contrasting evolutionary responses to avian malaria
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2613920/
https://www.ncbi.nlm.nih.gov/pubmed/19014596
http://dx.doi.org/10.1186/1471-2148-8-315
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