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

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 Lilia...

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Main Authors: Givnish, Thomas J., Zuluaga, Alejandro, Marques, Isabel, Lam, Vivienne K. Y., Soto Gomez, Marybel, 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.
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Language:unknown
Published: Zenodo 2016
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Online Access:https://doi.org/10.5061/dryad.mc736
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spelling ftzenodo:oai:zenodo.org:4999492 2024-09-15T17:43:22+00:00 Data from: 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. Soto Gomez, Marybel 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. 2016-12-18 https://doi.org/10.5061/dryad.mc736 unknown Zenodo https://doi.org/10.1111/cla.12153 https://zenodo.org/communities/dryad https://doi.org/10.5061/dryad.mc736 oai:zenodo.org:4999492 info:eu-repo/semantics/openAccess Creative Commons Zero v1.0 Universal https://creativecommons.org/publicdomain/zero/1.0/legalcode info:eu-repo/semantics/other 2016 ftzenodo https://doi.org/10.5061/dryad.mc73610.1111/cla.12153 2024-07-25T12:23:42Z 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. Alignments of 75 chloroplast coding regions for 135 Angiosperms Nexus file containing a concatenated alignment of 75 coding regions for 33 species of Liliales and other 102 Angiosperms. 135_Angiosperm_75CDS.nex XML BEAST file for divergence times estimation XML file for divergence times estimation analysis with BEAST v1.8.0. Liliales_2Genes_angiosperm.xml Other/Unknown Material Antarc* Antarctica Bering Land Bridge Zenodo
institution Open Polar
collection Zenodo
op_collection_id ftzenodo
language unknown
description 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. Alignments of 75 chloroplast coding regions for 135 Angiosperms Nexus file containing a concatenated alignment of 75 coding regions for 33 species of Liliales and other 102 Angiosperms. 135_Angiosperm_75CDS.nex XML BEAST file for divergence times estimation XML file for divergence times estimation analysis with BEAST v1.8.0. Liliales_2Genes_angiosperm.xml
format Other/Unknown Material
author Givnish, Thomas J.
Zuluaga, Alejandro
Marques, Isabel
Lam, Vivienne K. Y.
Soto Gomez, Marybel
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.
Soto Gomez, Marybel
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.
Data from: 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.
Soto Gomez, Marybel
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 Data from: Phylogenomics and historical biogeography of the monocot order Liliales: out of Australia and through Antarctica
title_short Data from: Phylogenomics and historical biogeography of the monocot order Liliales: out of Australia and through Antarctica
title_full Data from: Phylogenomics and historical biogeography of the monocot order Liliales: out of Australia and through Antarctica
title_fullStr Data from: Phylogenomics and historical biogeography of the monocot order Liliales: out of Australia and through Antarctica
title_full_unstemmed Data from: Phylogenomics and historical biogeography of the monocot order Liliales: out of Australia and through Antarctica
title_sort data from: phylogenomics and historical biogeography of the monocot order liliales: out of australia and through antarctica
publisher Zenodo
publishDate 2016
url https://doi.org/10.5061/dryad.mc736
genre Antarc*
Antarctica
Bering Land Bridge
genre_facet Antarc*
Antarctica
Bering Land Bridge
op_relation https://doi.org/10.1111/cla.12153
https://zenodo.org/communities/dryad
https://doi.org/10.5061/dryad.mc736
oai:zenodo.org:4999492
op_rights info:eu-repo/semantics/openAccess
Creative Commons Zero v1.0 Universal
https://creativecommons.org/publicdomain/zero/1.0/legalcode
op_doi https://doi.org/10.5061/dryad.mc73610.1111/cla.12153
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