The evolutionary history of Eryngium (Apiaceae, Saniculoideae): Rapid radiations, long distance dispersals, and hybridizations
Eryngium is the largest and arguably the most taxonomically complex genus in the family Apiaceae. Infrageneric relationships within Eryngium were inferred using sequence data from the chloroplast DNA trnQ-trnK 5′-exon and nuclear ribosomal DNA ITS regions to test previous hypotheses of subgeneric re...
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| 001 | PAPER-6069 | ||
| 003 | AR-BaUEN | ||
| 005 | 20230518203544.0 | ||
| 008 | 190411s2008 xx ||||fo|||| 00| 0 eng|d | ||
| 024 | 7 | |2 scopus |a 2-s2.0-40849098795 | |
| 024 | 7 | |2 Molecular Sequence Numbers |a GENBANK: EU070416, EU070417, EU070418, EU070419, EU070420; | |
| 024 | 7 | |2 cas |a DNA, Chloroplast | |
| 040 | |a Scopus |b spa |c AR-BaUEN |d AR-BaUEN | ||
| 030 | |a MPEVE | ||
| 100 | 1 | |a Calviño, C.I. | |
| 245 | 1 | 4 | |a The evolutionary history of Eryngium (Apiaceae, Saniculoideae): Rapid radiations, long distance dispersals, and hybridizations |
| 260 | |c 2008 | ||
| 270 | 1 | 0 | |m Calviño, C.I.; Instituto de Botánica Darwinion, CC22, B1642HYD, San Isidro, Buenos Aires, Argentina; email: ccalvino@life.uiuc.edu |
| 506 | |2 openaire |e Política editorial | ||
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| 520 | 3 | |a Eryngium is the largest and arguably the most taxonomically complex genus in the family Apiaceae. Infrageneric relationships within Eryngium were inferred using sequence data from the chloroplast DNA trnQ-trnK 5′-exon and nuclear ribosomal DNA ITS regions to test previous hypotheses of subgeneric relationships, explain distribution patterns, reconstruct ancestral morphological features, and elucidate the evolutionary processes that gave rise to this speciose genus. In total, 157 accessions representing 118 species of Eryngium, 15 species of Sanicula (including the genus Hacquetia that was recently reduced to synonymy) and the monotypic Petagnaea were analyzed using maximum parsimony and Bayesian methods. Both separate and simultaneous analyses of plastid and nuclear data sets were carried out because of the prevalence of polyploids and hybrids within the genus. Eryngium is confirmed as monophyletic and is divided into two redefined subgenera: Eryngium subgenus Eryngium and E. subgenus Monocotyloidea. The first subgenus includes all examined species from the Old World (Africa, Europe, and Asia), except Eryngium tenue, E. viviparum, E. galioides, and E. corniculatum. Eryngium subgenus Monocotyloidea includes all examined species from the New World (North, Central and South America, and Australia; herein called the "New World sensu stricto" clade) plus the aforementioned Old World species that fall at the base of this clade. Most sectional and subgeneric divisions previously erected on the basis of morphology are not monophyletic. Within the "New World sensu stricto" group, six clades are well supported in analyses of plastid and combined plastid and nuclear data sets; the relationships among these clades, however, are unresolved. These clades are designated as "Mexican", "Eastern USA", "South American", "North American monocotyledonous", "South American monocotyledonous", and "Pacific". Members of each clade share similar geographical distributions and/or morphological or ecological traits. Evidence from branch lengths and low sequence divergence estimates suggests a rapid radiation at the base of each of these lineages. Conflict between chloroplast and nuclear data sets is weak, but the disagreements found are suggestive that hybrid speciation in Eryngium might have been a cause, but also a consequence, of the different rapid radiations observed. Dispersal-vicariance analysis indicates that Eryngium and its two subgenera originated from western Mediterranean ancestors and that the present-day distribution of the genus is explained by several dispersal events, including one trans-Atlantic dispersal. In general, these dispersals coincide with the polytomies observed, suggesting that they played key roles in the diversification of the genus. The evolution of Eryngium combines a history of long distance dispersals, rapid radiations, and hybridization, culminating in the taxonomic complexity observed today in the genus. © 2007 Elsevier Inc. All rights reserved. |l eng | |
| 536 | |a Detalles de la financiación: National Science Foundation, DEB 0089452 | ||
| 536 | |a Detalles de la financiación: National Centre for Supercomputing Applications, DEB 030005N | ||
| 536 | |a Detalles de la financiación: Instytut Biologii Medycznej Polskiej Akademii Nauk | ||
| 536 | |a Detalles de la financiación: University of Illinois at Urbana-Champaign | ||
| 536 | |a Detalles de la financiación: Consejo Nacional de Investigaciones Científicas y Técnicas | ||
| 536 | |a Detalles de la financiación: The authors thank the curators of herbaria BA, CORD, CTES, E, ILL, ILLS, JACA, JEPS, MA, MO, PAL, SI, TEX-LL, UC, US, W, and WIS, for access to specimens, and F.O. Zuloaga and anonymous reviewers for comments on the manuscript. This work was supported by grants to S.R.D. from the National Science Foundation (DEB 0089452) and the National Center for Supercomputing Applications (DEB 030005N), utilizing the IBM pSeries 690 system at the University of Illinois at Urbana-Champaign (UIUC). Travel funds to C.I.C. were provided by UIUC’s School of Integrative Biology Enhancement Fund and the Department of Plant Biology John R. Laughnan Award. A collection trip to Paraguay (C.I.C. and S.G.M.) was supported by the Myndel Botanica Foundation. This paper represents part of a Ph.D. dissertation (C.I.C.), for which funding from CONICET is gratefully acknowledged. Appendix A | ||
| 593 | |a Instituto de Botánica Darwinion, CC22, B1642HYD, San Isidro, Buenos Aires, Argentina | ||
| 593 | |a Department of Plant Biology, University of Illinois at Urbana-Champaign, Urbana, IL 61801, United States | ||
| 593 | |a Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Argentina | ||
| 690 | 1 | 0 | |a APIACEAE |
| 690 | 1 | 0 | |a BIOGEOGRAPHY |
| 690 | 1 | 0 | |a CPDNA TRNQ-TRNK 5′-EXON |
| 690 | 1 | 0 | |a ERYNGIUM |
| 690 | 1 | 0 | |a LONG DISTANCE DISPERSALS |
| 690 | 1 | 0 | |a NRDNA ITS |
| 690 | 1 | 0 | |a PHYLOGENY |
| 690 | 1 | 0 | |a RAPID RADIATION |
| 690 | 1 | 0 | |a RETICULATE EVOLUTION |
| 690 | 1 | 0 | |a SANICULOIDEAE |
| 690 | 1 | 0 | |a CHLOROPLAST DNA |
| 690 | 1 | 0 | |a ARTICLE |
| 690 | 1 | 0 | |a CHEMISTRY |
| 690 | 1 | 0 | |a CLASSIFICATION |
| 690 | 1 | 0 | |a DNA SEQUENCE |
| 690 | 1 | 0 | |a ERYNGIUM |
| 690 | 1 | 0 | |a GENETICS |
| 690 | 1 | 0 | |a HYBRIDIZATION |
| 690 | 1 | 0 | |a MOLECULAR EVOLUTION |
| 690 | 1 | 0 | |a MOLECULAR GENETICS |
| 690 | 1 | 0 | |a NUCLEOTIDE SEQUENCE |
| 690 | 1 | 0 | |a PHYLOGENY |
| 690 | 1 | 0 | |a DNA, CHLOROPLAST |
| 690 | 1 | 0 | |a ERYNGIUM |
| 690 | 1 | 0 | |a EVOLUTION, MOLECULAR |
| 690 | 1 | 0 | |a HYBRIDIZATION, GENETIC |
| 690 | 1 | 0 | |a MOLECULAR SEQUENCE DATA |
| 690 | 1 | 0 | |a PHYLOGENY |
| 690 | 1 | 0 | |a SEQUENCE ANALYSIS, DNA |
| 690 | 1 | 0 | |a APIACEAE |
| 690 | 1 | 0 | |a APIALES |
| 690 | 1 | 0 | |a ERYNGIUM |
| 690 | 1 | 0 | |a ERYNGIUM VIVIPARUM |
| 690 | 1 | 0 | |a HACQUETIA |
| 690 | 1 | 0 | |a PETAGNAEA |
| 690 | 1 | 0 | |a SANICULA |
| 690 | 1 | 0 | |a SANICULOIDEAE |
| 700 | 1 | |a Martínez, S.G. | |
| 700 | 1 | |a Downie, S.R. | |
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