2015
DOI: 10.1111/jbi.12496
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Continental‐scale diversification patterns in a megadiverse genus: the biogeography of Neotropical Begonia

Abstract: Aim The origin of Neotropical hyperdiversity is one of the most intriguing questions in modern biogeography and is best answered through the investigation of large, pantropically distributed genera, allowing the comparison of closely related clades in different regions. We produced a dated phylogeny and reconstructed ancestral ranges of the megadiverse, Andean‐centred genus Begonia to discern its dispersal history throughout the Neotropics and correlates of range evolution. Neotropical and Palaeotropical diver… Show more

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Cited by 43 publications
(42 citation statements)
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“…An understanding of the age and patterns of diversification in these species would provide information on the development of the dry forest biome in Colombia and on when the geological/climatic conditions were appropriate for the development of a seasonally dry climate.4.3 | Cloud forestNeotropical cloud forests are restricted to altitudes of approximately 1,000 to 3,000 m. Lineages that are restricted to those altitudes would be expected to have begun to diversify from the crown node (the node in the phylogenetic tree at which point a lineage began to diversify) of the phylogeny at the age at which those altitudes were reached (Figure 1b) Moonlight et al (2015). Pennington and Dick (2010) indicated that populations of Cyathostegia mathewsii (Fabaceae) diversified in different Andean dry forests in Peru and Ecuador from c. 5.4 (+/−1.0) mya, with diversification within individual areas occurring from c. 2.8 (+/−0.6) mya.…”
mentioning
confidence: 99%
“…An understanding of the age and patterns of diversification in these species would provide information on the development of the dry forest biome in Colombia and on when the geological/climatic conditions were appropriate for the development of a seasonally dry climate.4.3 | Cloud forestNeotropical cloud forests are restricted to altitudes of approximately 1,000 to 3,000 m. Lineages that are restricted to those altitudes would be expected to have begun to diversify from the crown node (the node in the phylogenetic tree at which point a lineage began to diversify) of the phylogeny at the age at which those altitudes were reached (Figure 1b) Moonlight et al (2015). Pennington and Dick (2010) indicated that populations of Cyathostegia mathewsii (Fabaceae) diversified in different Andean dry forests in Peru and Ecuador from c. 5.4 (+/−1.0) mya, with diversification within individual areas occurring from c. 2.8 (+/−0.6) mya.…”
mentioning
confidence: 99%
“…) was most likely from the Madrean region during early Miocene (ca. 17 mya) and via LDD since the closure of the Panama Isthmus was not fully completed until 8 mya (Coates et al, ; Bacon et al, ; Montes et al, ). The existence of island arcs between the two continents at around 15 mya (Krzywinski et al, ) could have facilitated this LDD.…”
Section: Discussionmentioning
confidence: 99%
“…All three species are close relatives within section Gireoudia , one of three sections that together form a major clade of Central American Begonia (total 117 species, clade age 9.48 Ma [5.82–13.55 Ma, 95% highest posterior density, HPD], Moonlight et al . 2015). This clade is part of the large radiation of Neotropical Begonia (>600 species, clade age 12.46 Ma [7.87–17.24 Ma HPD] Moonlight et al .…”
Section: Methodsmentioning
confidence: 99%
“…This clade is part of the large radiation of Neotropical Begonia (>600 species, clade age 12.46 Ma [7.87–17.24 Ma HPD] Moonlight et al . 2015). …”
Section: Methodsmentioning
confidence: 99%