Historical biogeography and diversification within the Neotropical parrot genus Pionopsitta (Aves: Psittacidae)
By C. C. Ribas, Renato Gaban-Lima, C. Miyaki, J. Cracraft. 2005
119 citations recorded by the source corpus.
Subfields: Ecology, Evolution, Behavior and Systematics, Genetics, Paleontology
View Paper: https://www.semanticscholar.org/paper/bf83a890051bb7e708059198f6b8cfb654adbcba
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Ecology, Evolution, Behavior and Systematics
- J. Pirani
- Todd A. Castoe
- Juan M. Daza
- J. Campbell
- C. Janson
- C. C. Ribas
- Christopher L. Parkinson
- M. Sasa
In Genetics
- Fernando M. d'Horta
- Todd A. Castoe
- Juan M. Daza
- Andrés M. Cuervo
- J. Campbell
- A. Eckert
- C. Janson
- C. Dick
In Paleontology
- J. Pirani
- Fernando M. d'Horta
- Todd A. Castoe
- Juan M. Daza
- Andrés M. Cuervo
- J. Campbell
- C. C. Ribas
- Michael E. Alfaro
Citations in the corpus
- Phylogeny and comparative phylogeography of Sclerurus (Aves: Furnariidae) reveal constant and cryptic diversification in an old radiation of rain forest understorey specialists (2013, background): “3, Table 1), and divergence between S. guatemalensis clades occurred during Late Pliocene–Early Pleistocene (from 1.0 to 1.9 Ma; node 22; Fig.”
- Comparative phylogeography of pitvipers suggests a consensus of ancient Middle American highland biogeography (2009, methodology): “Accordingly, most studies have dealt with biogeographical patterns in the late Pliocene–Pleistocene relating to the establishment of the final land connection with South America (Stehli & Webb, 1985; Hafner, 1991; Webb, 1997), and relatively few have investigated earlier patterns in the Miocene and ”
- Explosive Pleistocene range expansion leads to widespread Amazonian sympatry between robust and gracile capuchin monkeys (2012, background): “We use genetic data to test whether Miocene or Plio-Pleistocene processes may explain capuchin species’ present distributions, and consider three possible scenarios to explain widespread sympatry.”
- Are the Northern Andes a species pump for Neotropical birds? Phylogenetics and biogeography of a clade of Neotropical tanagers (Aves: Thraupini) (2010, unknown): “Molecular-based phylogenies for birds of this region (e.g. Ribas et al., 2005; Aleixo & de Fátima Rossetti, 2007; Brumfield & Edwards, 2007) are just beginning to provide insight into the importance of these different processes (Bates et al., 2008).”
- Review of plant biogeographic studies in Brazil (2009, background): “…based on phylogenetic data comes from studies of birds (Cracraft, 1985; Cracraft & Prum, 1988; Marks et al., 2002; Eberhard & Bermingham, 2005; Ribas et al., 2005), butterflies (Hall & Harvey, 2002) and dipterans (Nihei & Carvalho, 2007 and references therein) and, to our understanding, the…”
- Avian gene trees, landscape evolution, and geology: towards a modern synthesis of Amazonian historical biogeography? (2007, background): “This situation changed a few years later, when the first studies with broader sampling regimes in Amazonia appeared (Hall and Harvey 2002; Marks et al. 2002; Symula et al. 2003; Ribas and Miyaki 2004; Armenta et al. 2005; Cheviron et al. 2005; Ribas et al. 2005, 2006 ).”
- The emerging field of geogenomics: Constraining geological problems with genetic data (2014, background): “Additionally, ages of diversification events in other Amazonian avian and primate groups that show strong spatial correlation between lineage distributions and large Amazonian rivers indicate that current species originated during the Plio-Pleistocene (Ribas et al., 2005; Boubli et al., 2012; d'Hort”