Morphological Phylogenetic Analysis of Basal Angiosperms: Comparison and Combination with Molecular Data

By J. Doyle, P. K. Endress. INTERNATIONAL JOURNAL PLANT SCIENCES, 2000

390 citations recorded by the source corpus.

Subfields: Ecology, Evolution, Behavior and Systematics, Molecular Biology

View Paper: https://www.semanticscholar.org/paper/ad9a635addf027af041045de2a064f2e7747ac09

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Citations in the corpus

Integrating Early Cretaceous Fossils into the Phylogeny of Living Angiosperms: ANITA Lines and Relatives of Chloranthaceae (2014, methodology): “Oil cells are absent in Amborella and Nymphaeales, and their origin is a presumed synapomorphy of Austrobaileyales and mesangiosperms (Doyle and Endress 2000).”
Phylogeny of Basal Angiosperms: Analyses of Five Genes from Three Genomes1 (2000, background): “…Kramer et al. 1998; Nandi et al. 1998; Hoot et al. 1999; Mathews and Donoghue 1999; Parkinson et al. 1999; Winter et al. 1999; Bowe et al. 2000; Doyle and Endress 2000; Frohlich and Parker 2000; Graham and Olmstead 2000; Sanderson et al. 2000; Savolainen et al. 2000; Barkman et al., in press).”
Morphological Phylogenetic Analysis of Living and Fossil Chloranthaceae (2004, methodology): “Characters adopted from Doyle and Endress (2000) are identified with ‘‘D&E’’ and the character numbers used in that study.”
Evolution of Floral Structures in Basal Angiosperms (2003, background): “Doyle and Endress (2000) found that in this case, morphological data were more supportive than molecular data in deciding that a single carpel is unequivocally derived in Laurales.”
Phylogeny of basal eudicots: Insights from non-coding and rapidly evolving DNA (2007, background): “Trochodendraceae and Tetracentraceae both share the lack of vessels as a prominent synapomorphy, a feature which now is understood as secondarily derived (Doyle and Endress 2000).”
Towards a phylogenetic nomenclature of Tracheophyta (2007, methodology): “Loss of oil cells in the mesophyll and dry fruit wall have also been identified as synapomorphies of /Eudicotyledoneae (Doyle & Endress, 2000, Fig.”
A metacalibrated time-tree documents the early rise of flowering plant phylogenetic diversity. (2015, background): “…(e.g. Soltis et al., 2011), and the as yet few, but increasing numbers of studies explicitly investigating their phylogenetic relationships (e.g. Doyle & Endress, 2000, 2010; Magall on, 2007; Mart ınez-Mill an et al., 2009; 2015 The Authors New Phytologist 2015 New Phytologist Trust New…”
Angiosperm Floral Evolution: Morphological Developmental Framework (2006, background): “, 2003) and studies of character evolution (Doyle and Endress, 2000; Ronse De Craene et al., 2003; Soltis et al., 2005b) appear to confirm this, because both phyllotaxis patterns are represented in this grade.”
Early evolution of angiosperm pollen as inferred from molecular and morphological phylogenetic analyses (2005, methodology): “In their aperture character (61), Doyle & Endress (2000) recognized one state, called trichotomosulcate, for three conditions: a sulcus Grana 44 (2005) with four to six branches in Hedyosmum (Chloranthaceae), three colpi usually fused at the distal pole (described as syntricolpate) in Illicium…”
Reproductive Structure and Organization of Basal Angiosperms from the Early Cretaceous (Barremian or Aptian) of Western Portugal (2000, methodology): “In the analysis of Doyle and Endress (2000), the family diverges one node above the ANITA grade, and in the analysis of Qiu et al. (1999), it diverges two nodes above the ANITA complex, after the Ceratophyllum-monocot group.”
Flower Structure and Trends of Evolution in Eudicots and Their Major Subclades1 (2010, background): “The presence of a perianth is certainly plesiomorphic in eudicots (cf. Doyle & Endress, 2000; Endress & Doyle, 2009).”
Floral Developmental Morphology of Amborella trichopoda (Amborellaceae) (2004, background): “Whether the ancestral perianth of angiosperms was differentiated or undifferentiated has been equivo- cal in previous character-state reconstructions (e.g., Doyle and Endress 2000; Ronse De Craene et al. 2003; Zanis et al. 2003).”
Phylogenetic Analyses of Basal Angiosperms Based on Nine Plastid, Mitochondrial, and Nuclear Genes (2005, background): “Qiu 91018; JL/LL/YQ; DQ008677 Qiu 91018; OD/FBQ/YQ; DQ008800 Murata et al. 2001; AB060736 Qiu 91018; OD/YQ; DQ008644 Thottea tomentosa Ding Hou Chase 1211, K; JL/LL/YQ; DQ008675 Chase 1211, K; OD/FBQ/YQ; DQ008797 Murata et al. 2001; AB060738 Chase 1211, K; OD/YQ; DQ008642 Asparagaceae: Asparagus off”
Phylogeny of Aristolochiaceae based on parsimony, likelihood, and Bayesian analyses of trnL-trnF sequences (2004, background): “Asaroideae comprise about 85 species and occur mainly in northern temperate regions with a centre of diversity in Asia (Kelly 1998), whereas Aristolochioideae have a predominantly tropical-subtropical distribution (Ma 1990).”
The Reproductive Structures of the Basal Angiosperm Amborella Trichopoda (Amborellaceae) (2000, background): “If Amborella and Monimiaceae are unrelated, as it appears in recent molecular and morphological phylogenetic studies (Qiu et al. 1999; Renner 1999; Doyle and Endress 2000), the similarities in floral structure, except for plesiomorphic features, are convergent.”
Dark and disturbed: a new image of early angiosperm ecology (2004, background): “Chloranthaceae, which occupied various near-basal positions in the molecular phylogenies just cited, branched immediately above this basal grade when molecular and morphological data were combined (Doyle and Endress 2000).”