The Great American Biotic Interchange revisited
By Sarah Cody, J. Richardson, V. Rull, C. Ellis, R. Pennington. 2010
194 citations recorded by the source corpus.
Subfields: Ecology, Evolution, Behavior and Systematics, Nature and Landscape Conservation
View Paper: https://www.semanticscholar.org/paper/f18e2cf619a265bef482b606a65e5fd1f81e8526
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
- Richard E. Olmstead
- Alexandre Antonelli
- Thomas L. P. Couvreur
- C. Hughes
- R. Pennington
- M. Weigend
- F. Luebert
- C. Bell
In Nature and Landscape Conservation
- Richard E. Olmstead
- Thomas L. P. Couvreur
- C. Hughes
- Alexandre Antonelli
- M. Weigend
- F. Luebert
- A. Muellner‐Riehl
- R. Pennington
Citations in the corpus
- Phylogeny and biogeography in Solanaceae, Verbenaceae and Bignoniaceae: a comparison of continental and intercontinental diversification patterns (2013, background): “…North America at c. 50–40 Mya, via GAARlandia (Greater Antilles and Aves Ridge) at c. 35–33 Mya (Morley, 2003; Pennington & Dick, 2004; Pirie et al., 2006) or via a Central American peninsula that reached close to north-western South America at c. 20–15 Mya (Cody et al., 2010; Montes et al., 2012).”
- The role of the uplift of the Qinghai‐Tibetan Plateau for the evolution of Tibetan biotas (2015, background): “It is clear, however, that biotic interchange contributed to the establishment of biodiversity hotspots, for example in the Andes (Cody et al., 2010) or on either side of Wallace’s Line (Lohman et al.”
- Phylogeny and comparative phylogeography of Sclerurus (Aves: Furnariidae) reveal constant and cryptic diversification in an old radiation of rain forest understorey specialists (2013, background): “Differences in divergence times across the isthmus have also been observed in other terrestrial organisms (Koepfi et al., 2007; Cody et al., 2010; Smith & Klicka, 2010; Johnson & Weckstein, 2011).”
- Pattern and timing of biogeographical history in the Neotropical tribe Bignonieae (Bignoniaceae) (2013, background): “The concentration of diversity in the Neotropics has attracted the attention of scientists, with considerable effort directed towards both the documentation of patterns and, more recently, a better understanding of the underlying processes (e.g. Pennington et al., 2004, 2010; Cody et al., 2010; Hoor”
- Neotropical Plant Evolution: Assembling the Big Picture (2013, background): “, 2010) that have shaped geographical dispersal opportunities and barriers through time, both large continental-scale ones separating South America from Africa and North America throughout much of the last 100 million years (Simpson, 1980; Stehli & Webb, 1985; Cody et al., 2010) and more regional on”
- Odd man out: why are there fewer plant species in African rain forests? (2014, background): “…North and South America via the Isthmus of Panama is also thought to have played a major role in diversification of TRFs with important biotic interchange and immigration followed by speciation (Bacon et al. 2013b; Cody et al. 2010; Erkens et al. 2007; Gentry 1982; Hughes and Eastwood 2006).”
- Phylogenetic insights into Andean plant diversification (2014, background): “Older ages for the closing of the Panama Isthmus have indeed been recently proposed by Farris et al. (2011), which has begun to be acknowledged by biogeographers (e.g., Antunes Carvalho and Renner, 2012; Hughes et al., 2013).”
- Testing geological models of evolution of the Isthmus of Panama in a phylogenetic framework (2013, unknown): “other angiosperms (Cody et al., 2010), freshwater fish (Bermingham & Martin, 1998) and salt-water-intolerant frogs (Weight et al.”