The Reproductive Structures of the Basal Angiosperm Amborella Trichopoda (Amborellaceae)

By P. K. Endress, A. Igersheim. INTERNATIONAL JOURNAL PLANT SCIENCES, 2000

105 citations recorded by the source corpus.

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

View Paper: https://www.semanticscholar.org/paper/4b158e5a985963464c170683bcbd5b52b12114e6

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In Ecology, Evolution, Behavior and Systematics

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Citations in the corpus

Disentangling confusions in inflorescence morphology: Patterns and diversity of reproductive shoot ramification in angiosperms (2010, background): “Among the basal angiosperms (ANITA grade), as currently conceived (e.g. Qiu et al., 1999; Soltis et al., 1999; Angiosperm Phylogeny Group, 2009), Amborella has (double) botryoids (Endress & Igersheim, 2000; Posluszny & Tomlinson, 2003).”
Floral Developmental Morphology of Amborella trichopoda (Amborellaceae) (2004, background): “This transition corresponds to what previous authors and we have observed in Amborella (Endress 1994c, 2001; Endress and Igersheim 2000; Posluszny and Tomlinson 2003).”
Phylogeny and evolutionary patterns in Nymphaeales: integrating genes, genomes and morphology (2008, background): “Carpel form is ascidiate in Nymphaeaceae except in Barclaya, where carpels appear plicate due to expansion of the floral center (Endress & Igersheim, 2000a), and also in Cabombaceae (Endress, 2005).”
Evolution of Floral Structures in Basal Angiosperms (2003, background): “Hesse M 2001 Pollen characters of Amborella trichopoda (Amborellaceae): a reinvestigation.”
Morphological Phylogenetic Analysis of Living and Fossil Chloranthaceae (2004, background): “…Wu (1980, 1982), Jérémie (1980, 1982b), D’Arcy and Liesner (1981), Wang et al. (1984), Verdcourt (1985, 1986, 1992), Todzia (1988, 1993), Todzia and Keating (1991), Yamazaki (1992), Zhou and Li (1994), Okada (1995), Endress and Igersheim (1997, 2000a), Luo and Li (1999), and Kong (2000a, 2001).”
Integrating Early Cretaceous Fossils into the Phylogeny of Living Angiosperms: ANITA Lines and Relatives of Chloranthaceae (2014, background): “The ancestral sulcus was modified to a several-armed furrow in the Asteropollis-Hedyosmum clade and to scattered pores and several colpoid areas in Sarcandra and Chloranthus, respectively.”
Flower Evolution: The Origin and Subsequent Diversification of the Angiosperm Flower (2009, background): “…that separates angiosperms from their gymnosperm relatives, although fully closed (that is, fused) carpels are neither found in Amborella nor in several other early diverging angiosperm lineages (for example Trimenia, Austrobaileya, Chloranthaceae) (Endress 2001a; Endress & Igersheim 2000a, 2000b).”
Morphological Phylogenetic Analysis of Basal Angiosperms: Comparison and Combination with Molecular Data (2000, background): “Degeneria: Bailey and Smith (1942); Myristicaceae: Vander Wyk and Canright (1956); Winteraceae: separate strands in Tasmannia, Drimys assumed to be ancestral; Amborella: cylinder composed entirely of U-shaped sclereids (Money et al. 1950) scored either 1 or 2; Chloranthaceae: Swamy (1953); Idiosperm”
Reproductive Structure and Organization of Basal Angiosperms from the Early Cretaceous (Barremian or Aptian) of Western Portugal (2000, background): “—BASAL ANGIOSPERMS FROM THE EARLY CRETACEOUS S179 cate, known from extant basal angiosperms (see Endress and Igersheim 2000a), and we have not attempted to evaluate this feature for the fossil material.”
The Flowers in Extant Basal Angiosperms and Inferences on Ancestral Flowers (2001, background): “The carpels are not postgenitally fused but filled with secretion (angiospermy type 1; Igersheim and Endress 1997; Endress and Igersheim 2000a).”