Phylogeny and Evolution of Angiosperms

By D. Soltis, Pamela S. Soltis, P. K. Endress, Mark W. Chase. 2005

439 citations recorded by the source corpus.

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Citations in the corpus

Integrating Molecular Phylogenetic and Paleobotanical Evidence on Origin of the Flower (2008, background): “The main uncertainty is whether Amborella and Nymphaeales form two successive lines or a clade, with more data favoring the former arrangement (Zanis et al. 2002; Soltis et al. 2005; Moore et al. 2007).”
Unraveling ancient hexaploidy through multiply-aligned angiosperm gene maps. (2008, result): “One phylogenetic model placed Vitis within the eurosid I clade (Jaillon et al. 2007), in contrast with the prevailing view of the Vitaceae as sister to both eurosid I and eurosid II (Davies et al. 2004; Soltis et al. 2005).”
Developmental Gene Evolution and the Origin of Grass Inflorescence Diversity (2006, background): “Over the last 15 years, increasingly robust phylogenies have become available for increasing numbers of taxa (Soltis et al., 2005; Stevens, 2001 onwards).”
Eastern Asian endemic seed plant genera and their paleogeographic history throughout the Northern Hemisphere (2009, background): “Although formerly placed in the Staphyleaceae, molecular and morphological studies indicate that Tapiscia, and the neotropical genus Huertea, form an unrelated family (Soltis et al., 2005).”
Comparative floral structure and systematics in Celastrales (Celastraceae, Parnassiaceae, Lepidobotryaceae) (2005, methodology): “In a summary tree by Soltis et al. (2005), based on Savolainen et al. (1994, 2000), Savolainen, Spichiger & Manen (1997), Soltis et al. (2000) and Simmons et al. (2001a), Rosales, Zygophyllaceae plus Krameriaceae, Huaceae, Malpighiales and (Oxalidales + Celastrales) are represented as a polytomy.”
Global stingless bee phylogeny supports ancient divergence, vicariance, and long distance dispersal (2009, background): “…than the oldest known bee-like fossil, Melittosphex burmensis (100 Mya; Poinar & Danforth, 2006), or at least younger than the radiation of the angiosperms (125 Mya; Morley, 2003; Soltis et al., 2005), which may have prompted the early radiation of bees (Grimaldi, 1999; Grimaldi & Engel, 2005).”
Historical biogeography and character evolution of Cistaceae (Malvales) based on analysis of plastid rbcL and trnL-trnF sequences (2009, background): “– Ducousso et al. (2004) – AY157715 Sphaerosepalaceae Rhopalocarpus Coger Rhopalocarpus sp. – Fay et al. (1998) – Y15148 * Plant material from The Royal Botanic Gardens, Kew, DNA Bank (www.rbgkew.org.uk/data/dnaBank/homepage.html).”
Tree of life for the genera of Chinese vascular plants (2016, background): “Within fabids (77% BS), three subclades were recovered, one of which is the nitrogen-fixing clade (Soltis et al., 1995, 2005), which contains Fabales (Fabaceae 99% BS; Polygalaceae 100% BS; Surianaceae); Rosales (Rhamnaceae 89% BS; Urticaceae 96% BS; Cannabaceae 98% BS; Rosaceae 99% BS;…”
Floral Diagrams: An Aid to Understanding Flower Morphology and Evolution (2010, unknown): “The most recent major textbooks on angiosperm phylogeny (e.g. Judd et al., 2002; Soltis et al., 2005; Simpson, 2006) lack any floral diagrams.”
Integrating Early Cretaceous Fossils into the Phylogeny of Living Angiosperms: ANITA Lines and Relatives of Chloranthaceae (2014, background): “This modest increase in support for a closer relationship between Chloranthaceae and Piperales must be weighed against increasingly strong molecular evidence for the monophyly of magnoliids and the nested position of Piperales within them (cf. Soltis et al. 2005).”
Phylogenetic Distribution and Identification of Fin-winged Fruits (2010, methodology): “Also considered here are examples from the Tertiary fossil record identified as Hernandiaceae, Polygonaceae, Rhamnaceae, Rutaceae, and Sapindaceae.”
Xylem heterochrony: an unappreciated key to angiosperm origin and diversifications. (2009, background): “Such families include Acanthaceae (3510 species) Asteraceae (23 000), Brassicaceae (3850), Euphorbiaceae (7000), Lamiaceae (6700), Malvaceae (2967) and Melastomaceae (4830) (species numbers from Soltis et al., 2007).”
The cleistogamous breeding system: A review of its frequency, evolution, and ecology in angiosperms (2007, background): “Similarly, Stewart (1994) suggested that increased allocation to CH reproduction may increase geitonogamy, resulting in diminished fitness gains because cross-fertilization is less likely.”
Rates of Molecular Evolution Are Linked to Life History in Flowering Plants (2008, background): “Onthebasis of our trees and broader phylogenetic studies of angiosperms [reviewed in ( 28 ); see also ( 29 )], the likely direction of evolution of plant habit was from trees/shrubs to the herbaceous condition in Apiales, Dipsacales, and Primulales, and with less certainly in Moraceae/Urticaceae.”
Integrating Early Cretaceous fossils into the phylogeny of living angiosperms: Magnoliidae and eudicots (2010, background): “Since 1999 (Mathews & Donoghue, 1999; Parkinson et al., 1999; Qiu et al., 1999, 2006; Soltis et al., 1999, 2000, 2005; Barkman et al., 2000; Graham & Olmstead, 2000; Zanis et al., 2002), such analyses have continued to reveal the same rooting of the angiosperm tree, among the so-called ANITA…”