It appears you don't have support to open PDFs in this web browser. To view this file, Open with your PDF reader
Abstract
Island systems provide important contexts for studying processes underlying lineage migration, species diversification, and organismal extinction. The Hawaiian endemic mints (Lamiaceae family) are the second largest plant radiation on the isolated Hawaiian Islands. We generated a chromosome-scale reference genome for one Hawaiian species, Stenogyne calaminthoides, and resequenced 45 relatives, representing 34 species, to uncover the continental origins of this group and their subsequent diversification. We further resequenced 109 individuals of two Stenogyne species, and their purported hybrids, found high on the Mauna Kea volcano on the island of Hawai’i. The three distinct Hawaiian genera, Haplostachys, Phyllostegia, and Stenogyne, are nested inside a fourth genus, Stachys. We uncovered four independent polyploidy events within Stachys, including one allopolyploidy event underlying the Hawaiian mints and their direct western North American ancestors. While the Hawaiian taxa may have principally diversified by parapatry and drift in small and fragmented populations, localized admixture may have played an important role early in lineage diversification. Our genomic analyses provide a view into how organisms may have radiated on isolated island chains, settings that provided one of the principal natural laboratories for Darwin’s thinking about the evolutionary process.
Hawaiian endemic mints represent the second largest plant radiation in the archipelago. Here, the authors present a reference genome and numerous resequenced individuals to uncover evidence for polyploidy, geographic speciation and localized hybridization underlying diversification in this lineage
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details
; Sebesta, Jeanne Theresa 1 ; Scheen, Anne-Cathrine 3 ; Bendiksby, Mika 4 ; Low, Yee Wen 5
; Salojärvi, Jarkko 2 ; Michael, Todd P. 6
; Albert, Victor A. 1
; Lindqvist, Charlotte 1
1 University at Buffalo, Department of Biological Sciences, New York, USA (GRID:grid.273335.3) (ISNI:0000 0004 1936 9887)
2 Nanyang Technological University, School of Biological Sciences, Singapore, Singapore (GRID:grid.59025.3b) (ISNI:0000 0001 2224 0361); University of Helsinki, Organismal and Evolutionary Biology Research Programme, Faculty of Biological and Environmental Sciences, Helsinki, Finland (GRID:grid.7737.4) (ISNI:0000 0004 0410 2071)
3 Stavanger Botanic Garden, City of Stavanger, Norway (GRID:grid.273335.3)
4 University of Oslo, Natural History Museum, Oslo, Norway (GRID:grid.5510.1) (ISNI:0000 0004 1936 8921)
5 National Parks Board, Singapore Botanic Gardens, Singapore, Singapore (GRID:grid.467827.8) (ISNI:0000 0004 0620 8814)
6 Salk Institute for Biological Studies, The Plant Molecular and Cellular Biology Laboratory, California, USA (GRID:grid.250671.7) (ISNI:0000 0001 0662 7144)




