An evaluation of new parsimony‐based versus parametric inference methods in biogeography: a case study using the globally distributed plant family Sapindaceae

By S. Buerki, Félix Forest, Nadir Alvarez, Johan A. A. Nylander, Nils Arrigo, I. Sanmartín. 2011

195 citations recorded by the source corpus.

Subfields: Ecology, Evolution, Behavior and Systematics, Nature and Landscape Conservation, Paleontology

View Paper: https://www.semanticscholar.org/paper/ec5470c079d76d0ae443568f92e873c0122fe1da

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

In Nature and Landscape Conservation

In Paleontology

Citations in the corpus

Global biogeography and diversification of palms sheds light on the evolution of tropical lineages. II. Diversification history and origin of regional assemblages (2013, background): “Dispersal events between these areas were inferred by comparing ancestral areas reconstructions at adjacent nodes (Ree & Smith, 2008; Buerki et al., 2011) and were collated to explore the biogeographical history of regional palm assemblages.”
Historical Biogeography: Evolution in Time and Space (2012, background): “This can be done by either adding new parameters to the transition matrix, or by scaling a global dispersal or extinction rate according to abiotic factors like geographic distance, the availability of land connections, or the strength of wind and ocean currents (Buerki et al. 2011).”
Global biogeography and diversification of palms sheds light on the evolution of tropical lineages. I. Historical biogeography (2013, methodology): “, 1994), adding to the mounting evidence that dispersal, in contrast to Gondwanan vicariance (Moore, 1973a; Raven & Axelrod, 1974), is a major mechanism behind the pantropical distribution of certain tropical rain forest plant families (Kress & Specht, 2006; Muellner et al., 2006; Bartish et al., 20”
Bayesian analysis of biogeography when the number of areas is large. (2013, background): “This phenomenon is also characteristic of other parsimony- and likelihoodbased biogeographic methods (e.g., Ronquist 1997; Ree et al. 2005; Clark et al. 2008; Buerki et al. 2011).”
Biogeographical patterns of plants in the Neotropics – dispersal rather than plate tectonics is most explanatory (2013, background): “, 2004), Lauraceae (Chanderbali, van der Werff & Renner, 2001), Sapindaceae (Buerki et al., 2011) and Phyllanthaceae (Wurdack, Hoffmann & Chase, 2005), all families with relatively large seeds, but in which all major clades have representatives on several major landmasses and are thought to have dis”
Bayesian estimation of the global biogeographical history of the Solanaceae (2017, result): “Our divisions are similar to those used in other studies of widespread clades (e.g. Buerki et al., 2011; Sessa et al., 2012) and will allow us to detect intercontinental movements as well as shorter range dispersal events (e.g. South America to the Caribbean).”
The historical biogeography of coral reef fishes: global patterns of origination and dispersal (2013, methodology): “Most notable is the congruence with global patterns of dispersal with terrestrial plants, where Australia and the IAA support numerous lineages with extensive evidence of dispersal from the Miocene onwards (Buerki et al., 2011).”
Biogeography and diversification of colletid bees (Hymenoptera: Colletidae): emerging patterns from the southern end of the world (2012, methodology): “1) was used for all Lagrange calculations and the root node of the tree was calibrated to 123 Ma, the point estimate age of the most recent ancestor of all terminal taxa considered.”
Temporal and spatial origin of Gesneriaceae in the New World inferred from plastid DNA sequences (2013, background): “Examples of such dispersals have been reconstructed for several lineages in Malvaceae, Myrtaceae, Sapindaceae, Sapotaceae and Nothofagus Blume (Baum et al., 2004; Sytsma et al., 2004; Knapp et al., 2005; Bartish et al., 2011; Buerki et al., 2011).”
Model selection in historical biogeography reveals that founder-event speciation is a crucial process in Island Clades. (2014, background): “It can be seen that the DEC model reconstructs several ancestral nodes with widespread ranges (a well-known bias of the model; Clark et al. 2008; Ree and Smith 2008; Buerki et al. 2011), which then break up through vicariance to produce daughter lineages with narrow ranges.”
Phylogenetic Methods in Biogeography (2011, background): “…peripheral isolate favor vicariance over dispersal when data are scarce, which results in association of deep nodes with wide distributions, whereas dispersals are biased toward terminal branches (Ree et al. 2005, Sanmartı́n 2007, Nylander et al. 2008, Kodandaramaiah 2010, Buerki et al. 2011).”
Late Cretaceous–Early Eocene origin of yams (Dioscorea, Dioscoreaceae) in the Laurasian Palaearctic and their subsequent Oligocene–Miocene diversification (2016, background): “1; see Appendix S1) and palaeogeography/plate tectonic history (cf. Bartish et al., 2011; Buerki et al., 2011).”