Tracing the impact of the Andean uplift on Neotropical plant evolution

By Alexandre Antonelli, Johan A. A. Nylander, C. Persson, I. Sanmartín. Proceedings of the National Academy of Sciences of the United States of America, 2009

625 citations recorded by the source corpus.

Subfields: Ecology, Evolution, Behavior and Systematics

View Paper: https://www.semanticscholar.org/paper/e30fd1bdb227af8afbfe86e845c00300b27afad5

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In Ecology, Evolution, Behavior and Systematics

Citations in the corpus

Phylogenetic insights into Andean plant diversification (2014, background): “The WAP was an East-West corridor located around the present Ecuadorian/Peruvian border (i.e., the Amotape- Huancabamba zone) that enabled Pacific marine incursions into the Amazonian basin until the Middle Miocene, when the marine incursions ceased due to Andean uplift (Hoorn, 1993).”
An evaluation of new parsimony‐based versus parametric inference methods in biogeography: a case study using the globally distributed plant family Sapindaceae (2011, methodology): “To date, Bayes-DIVA has been used in several empirical plant studies dealing with regional scenarios (e.g. Antonelli et al. , 2009; Roquet et al. , 2009; Espı´ndola et al. , 2010).”
Global biogeography and diversification of palms sheds light on the evolution of tropical lineages. II. Diversification history and origin of regional assemblages (2013, background): “Boreotropical dispersal routes between major tropical regions have been documented in several other pantropical families, including Annonaceae (Erkens et al., 2009; Couvreur et al., 2011b), Malpighiaceae (Davis et al., 2002), Meliaceae (Muellner et al., 2006), Melastomataceae (Renner & Meyer, 2001) ”
Early evolutionary history of the flowering plant family Annonaceae: steady diversification and boreotropical geodispersal (2011, neutral): “…for example in Malpighiaceae (Davis et al., 2002), Meliaceae (Muellner et al., 2006), Melastomataceae s. str. (Renner et al., 2001) and Rubiaceae (Antonelli et al., 2009), all indicate that these families have tropical disjunctions with lineages splitting up at a time consistent with the…”
The changing course of the Amazon River in the Neogene: center stage for Neotropical diversification (2018, background): “…origins in the super-greenhouse world of the Late Cretaceous (100-66 Ma) and Paleogene (66-23 Ma), and the biota achieved approximately modern dimensions during the Neogene (23-2.6 Ma; Lundberg et al ., 1998; Antonelli et al ., 2009, 2010; Albert et al ., 2011b; López-Fernández, Albert, 2011).”
Pattern and timing of biogeographical history in the Neotropical tribe Bignonieae (Bignoniaceae) (2013, background): “They indicate that different biogeographical and environmental factors are important in different lineages (e.g. Pennington et al., 2004; Särkinen et al., 2007; Antonelli et al., 2009; Roncal et al., 2010), and that overall patterns reflect the complex history of Neotropical environments (Antonelli ”
The radiation of Satyrini butterflies (Nymphalidae: Satyrinae): a challenge for phylogenetic methods (2011, background): “It has been hypothesized that this land bridge was also important in the evolution of Phyciodina butterflies (Nymphalidae) (Wahlberg & Freitas, 2007) and plants in the coffee family (Rubiaceae) (Antonelli et al., 2009).”
Vicariance or long‐distance dispersal: historical biogeography of the pantropical subfamily Chrysophylloideae (Sapotaceae) (2011, background): “…et al., 2009), Burseraceae (Weeks et al., 2005), Campanulaceae (Antonelli, 2009), Ebenaceae (Duangjai et al., 2009), Malpighiaceae (Davis et al., 2002), Melastomataceae (Renner et al., 2001), Meliaceae (Muellner et al., 2006), Moraceae (Zerega et al., 2005) and Rubiaceae (Antonelli et al., 2009).”
Temporal and spatial origin of Gesneriaceae in the New World inferred from plastid DNA sequences (2013, background): “To date, few studies have investigated the genesis of this pattern (Pirie et al., 2006; Antonelli et al., 2009; Givnish et al., 2011), despite its importance for identifying the biotic or abiotic factors that may have shaped the spatial distribution of diversity we see today (Antonelli & Sanmartín,…”
Why are there so many plant species in the Neotropics (2011, background): “Simplified landscape evolution of northern South America in the last 35 Ma (adapted from Antonelli et al., 2009; Hoorn & al., 2010).”
Neotropical Plant Evolution: Assembling the Big Picture (2013, background): “Fourteen of the 16 papers in this issue use phylogenetic evidence to infer patterns of diversification, and many other new phylogenetic analyses published in the last eight years have provided insights into geotemporal patterns of Neotropical plant diversification (e.g. Hughes & Eastwood, 2006; Anto”
Historical biogeography and life‐history evolution of Andean Puya (Bromeliaceae) (2013, background): “The WAP presented a potentially important barrier to many groups of organisms (Vuilleumier, 1969; Duellman, 1979; Ayers, 1999; Andersson, 2006; Antonelli et al., 2009; Cosacov et al., 2009) and is an area exhibiting high endemism for many other groups (Berry, 1982; Weigend, 2002; Smith & Baum,…”
A tale of migrations from east to west: the Irano‐Turanian floristic region as a source of Mediterranean xerophytes (2014, background): “Orogenic activities, especially mountain uplifts, have been shown to contribute crucially to processes of floristic diversification (Hughes & Eastwood, 2006; Antonelli et al., 2009).”
Why mountains matter for biodiversity (2019, background): “Available data indicate that some mountain systems, such as the Southern Alps in New Zealand and parts of the Andes in South America (Garzione et al., 2008; Mulch, 2016) and the Himalaya in Asia (see overview in Spicer, 2017), have uplifted quickly and rel - atively recently (in the past 15 Ma).”