Phylogenomics and historical biogeography of the monocot order Liliales: out of Australia and through Antarctica

Abstract We present the first phylogenomic analysis of relationships among all ten families of Liliales, based on 75 plastid genes from 35 species in 29 genera, and 97 additional plastomes stratified across angiosperm lineages. We used a supermatrix approach to extend our analysis to 58 of 64 genera...

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Published in:Cladistics
Main Authors: Givnish, Thomas J., Zuluaga, Alejandro, Marques, Isabel, Lam, Vivienne K. Y., Gomez, Marybel Soto, Iles, William J. D., Ames, Mercedes, Spalink, Daniel, Moeller, Jackson R., Briggs, Barbara G., Lyon, Stephanie P., Stevenson, Dennis W., Zomlefer, Wendy, Graham, Sean W.
Other Authors: Natural Sciences and Engineering Research Council of Canada, Seventh Framework Programme
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 2016
Subjects:
Online Access:http://dx.doi.org/10.1111/cla.12153
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spelling crwiley:10.1111/cla.12153 2024-10-13T14:01:29+00:00 Phylogenomics and historical biogeography of the monocot order Liliales: out of Australia and through Antarctica Givnish, Thomas J. Zuluaga, Alejandro Marques, Isabel Lam, Vivienne K. Y. Gomez, Marybel Soto Iles, William J. D. Ames, Mercedes Spalink, Daniel Moeller, Jackson R. Briggs, Barbara G. Lyon, Stephanie P. Stevenson, Dennis W. Zomlefer, Wendy Graham, Sean W. Natural Sciences and Engineering Research Council of Canada Seventh Framework Programme 2016 http://dx.doi.org/10.1111/cla.12153 https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fcla.12153 https://onlinelibrary.wiley.com/doi/pdf/10.1111/cla.12153 en eng Wiley http://onlinelibrary.wiley.com/termsAndConditions#vor Cladistics volume 32, issue 6, page 581-605 ISSN 0748-3007 1096-0031 journal-article 2016 crwiley https://doi.org/10.1111/cla.12153 2024-09-17T04:49:37Z Abstract We present the first phylogenomic analysis of relationships among all ten families of Liliales, based on 75 plastid genes from 35 species in 29 genera, and 97 additional plastomes stratified across angiosperm lineages. We used a supermatrix approach to extend our analysis to 58 of 64 genera of Liliales, and calibrated the resulting phylogeny against 17 fossil dates to produce a new timeline for monocot evolution. Liliales diverged from other monocots 124 Mya and began splitting into separate families 113 Mya. Our data support an Australian origin for Liliales, with close relationships between three pairs of lineages (Corsiaceae/Campynemataceae, Philesiaceae/Ripogonaceae, tribes Alstroemerieae/Luzuriageae) in South America and Australia or New Zealand reflecting teleconnections of these areas via Antarctica. Long‐distance dispersal ( LDD ) across the Pacific and Tasman Sea led to re‐invasion of New Zealand by two lineages ( Luzuriaga, Ripogonum ); LDD allowed Campynemanthe to colonize New Caledonia after its submergence until 37 Mya. LDD permitted Colchicaceae to invade East Asia and Africa from Australia, and re‐invade Africa from Australia. Periodic desert greening permitted Gloriosa and Iphigenia to colonize Southeast Asia overland from Africa, and Androcymbium–Colchicum to invade the Mediterranean from South Africa. Melanthiaceae and Liliaceae crossed the Bering land‐bridge several times from the Miocene to the Pleistocene. Article in Journal/Newspaper Antarc* Antarctica Bering Land Bridge Wiley Online Library Pacific New Zealand Cladistics 32 6 581 605
institution Open Polar
collection Wiley Online Library
op_collection_id crwiley
language English
description Abstract We present the first phylogenomic analysis of relationships among all ten families of Liliales, based on 75 plastid genes from 35 species in 29 genera, and 97 additional plastomes stratified across angiosperm lineages. We used a supermatrix approach to extend our analysis to 58 of 64 genera of Liliales, and calibrated the resulting phylogeny against 17 fossil dates to produce a new timeline for monocot evolution. Liliales diverged from other monocots 124 Mya and began splitting into separate families 113 Mya. Our data support an Australian origin for Liliales, with close relationships between three pairs of lineages (Corsiaceae/Campynemataceae, Philesiaceae/Ripogonaceae, tribes Alstroemerieae/Luzuriageae) in South America and Australia or New Zealand reflecting teleconnections of these areas via Antarctica. Long‐distance dispersal ( LDD ) across the Pacific and Tasman Sea led to re‐invasion of New Zealand by two lineages ( Luzuriaga, Ripogonum ); LDD allowed Campynemanthe to colonize New Caledonia after its submergence until 37 Mya. LDD permitted Colchicaceae to invade East Asia and Africa from Australia, and re‐invade Africa from Australia. Periodic desert greening permitted Gloriosa and Iphigenia to colonize Southeast Asia overland from Africa, and Androcymbium–Colchicum to invade the Mediterranean from South Africa. Melanthiaceae and Liliaceae crossed the Bering land‐bridge several times from the Miocene to the Pleistocene.
author2 Natural Sciences and Engineering Research Council of Canada
Seventh Framework Programme
format Article in Journal/Newspaper
author Givnish, Thomas J.
Zuluaga, Alejandro
Marques, Isabel
Lam, Vivienne K. Y.
Gomez, Marybel Soto
Iles, William J. D.
Ames, Mercedes
Spalink, Daniel
Moeller, Jackson R.
Briggs, Barbara G.
Lyon, Stephanie P.
Stevenson, Dennis W.
Zomlefer, Wendy
Graham, Sean W.
spellingShingle Givnish, Thomas J.
Zuluaga, Alejandro
Marques, Isabel
Lam, Vivienne K. Y.
Gomez, Marybel Soto
Iles, William J. D.
Ames, Mercedes
Spalink, Daniel
Moeller, Jackson R.
Briggs, Barbara G.
Lyon, Stephanie P.
Stevenson, Dennis W.
Zomlefer, Wendy
Graham, Sean W.
Phylogenomics and historical biogeography of the monocot order Liliales: out of Australia and through Antarctica
author_facet Givnish, Thomas J.
Zuluaga, Alejandro
Marques, Isabel
Lam, Vivienne K. Y.
Gomez, Marybel Soto
Iles, William J. D.
Ames, Mercedes
Spalink, Daniel
Moeller, Jackson R.
Briggs, Barbara G.
Lyon, Stephanie P.
Stevenson, Dennis W.
Zomlefer, Wendy
Graham, Sean W.
author_sort Givnish, Thomas J.
title Phylogenomics and historical biogeography of the monocot order Liliales: out of Australia and through Antarctica
title_short Phylogenomics and historical biogeography of the monocot order Liliales: out of Australia and through Antarctica
title_full Phylogenomics and historical biogeography of the monocot order Liliales: out of Australia and through Antarctica
title_fullStr Phylogenomics and historical biogeography of the monocot order Liliales: out of Australia and through Antarctica
title_full_unstemmed Phylogenomics and historical biogeography of the monocot order Liliales: out of Australia and through Antarctica
title_sort phylogenomics and historical biogeography of the monocot order liliales: out of australia and through antarctica
publisher Wiley
publishDate 2016
url http://dx.doi.org/10.1111/cla.12153
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fcla.12153
https://onlinelibrary.wiley.com/doi/pdf/10.1111/cla.12153
geographic Pacific
New Zealand
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New Zealand
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Antarctica
Bering Land Bridge
genre_facet Antarc*
Antarctica
Bering Land Bridge
op_source Cladistics
volume 32, issue 6, page 581-605
ISSN 0748-3007 1096-0031
op_rights http://onlinelibrary.wiley.com/termsAndConditions#vor
op_doi https://doi.org/10.1111/cla.12153
container_title Cladistics
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