See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/43181884 S-DIVA (Statistical Dispersal-Vicariance Analysis): A tool for inferring biogeographic histories Article in Molecular Phylogenetics and Evolution · August 2010 DOI: 10.1016/j.ympev.2010.04.011 · Source: PubMed CITATIONS READS 584 2,339 3 authors: Yan Yu Aj Harris Sichuan University South China Botanical Garden 84 PUBLICATIONS 1,749 CITATIONS 65 PUBLICATIONS 1,731 CITATIONS SEE PROFILE SEE PROFILE Xing-Jin He Sichuan University 228 PUBLICATIONS 2,870 CITATIONS SEE PROFILE Some of the authors of this publication are also working on these related projects: Diversification, diversity, and biogeography of Acer L., particularly in North America View project Molecular phylogeny; Evolutionary History; Floral Genome Project; Taxionamy View project All content following this page was uploaded by Xing-Jin He on 12 March 2019. 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Authors requiring further information regarding Elsevier’s archiving and manuscript policies are encouraged to visit: http://www.elsevier.com/copyright Author's personal copy Molecular Phylogenetics and Evolution 56 (2010) 848–850 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev Short Communication S-DIVA (Statistical Dispersal-Vicariance Analysis): A tool for inferring biogeographic histories Yan Yu a, A.J. Harris b, Xingjin He a,* a b College of Life Sciences, Sichuan University, Chengdu 610064, China Curriculum for the Environment and Ecology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA a r t i c l e i n f o Article history: Received 4 December 2009 Revised 10 March 2010 Accepted 6 April 2010 Available online 22 April 2010 Keywords: DIVA Biogeographic Program Phylogeny Statistics a b s t r a c t Dispersal-Vicariance Analysis (DIVA) is one of the most widely used methods of inferring biogeographic histories. Here we present a simple tool that complements DIVA and uses a Statistical Dispersal-Vicariance Analysis (S-DIVA) to statistically evaluate the alternative ancestral ranges at each node in a tree accounting for phylogenetic uncertainty and uncertainty in DIVA optimization. S-DIVA provides a point-and-click user interface and displays results as, high-resolution, exportable graphics. S-DIVA is freely available for download for Windows at http://mnh.scu.edu.cn/S-DIVA. Ó 2010 Elsevier Inc. All rights reserved. 1. Introduction Studies in historical biogeography based on phylogeny have accumulated rapidly in the literature due to the exponential increase in phylogenetic studies (see Xiang et al., 1998, 2004, 2005, 2006; Wen, 1999; Sanmartín et al., 2001; Donoghue and Smith, 2004; Sanmartín and Ronquist, 2004; Soltis et al., 2006; Harris et al., 2009; Alexandre et al., 2009). Dispersal-Vicariance Analysis (DIVA) (Ronquist, 1997, 2001) is one of the most widely used methods of inferring biogeographic histories. This is evidenced by an advanced Google scholar search for ‘‘DIVA” and ‘‘biogeography” in 2009 returning greater than 50 relevant results. DIVA reconstructs the ancestral distribution in a phylogeny by optimizing a three-dimensional cost matrix, in which extinctions and dispersals ‘‘cost” more than vicariance (Ronquist, 1997; Lamm and Redelings, 2009). Although model-based methods for inferring biogeography are available (e.g., Ree et al., 2005; Ree and Smith, 2008; Sanmartín et al., 2008), DIVA remains popular because it provides rapid results, requires little prior information, and gives results comparable to the model-based likelihood method Lagrange of Ree et al. (2005) and Ree and Smith (2008) (e.g., Ree et al., 2005; Burbrink and Lawson, 2007; Ree and Smith, 2008; Velazco and Patterson, 2008; Xiang et al., 2008; Xiang et al., 2009). One problem with the current implementation of DIVA is that it ignores the uncertainty in phylogenetic inference because ancestral ranges are reconstructed onto a fixed tree topology assumed to be * Corresponding author. Fax: +86 02885415006. E-mail address: xjhe@scu.edu.cn (X. He). 1055-7903/$ - see front matter Ó 2010 Elsevier Inc. All rights reserved. doi:10.1016/j.ympev.2010.04.011 without error (Nylander et al., 2008). A second source of uncertainty in DIVA is that associated with ancestral area optimization; multiple equally optimal reconstructions often result in multiple ranges suggested at ancestral nodes (Ronquist, 1997; Nylander et al., 2008). To account for these uncertainties, Nylander et al. (2008) recently showed the utility of a non-parametric empirical Bayesian approach to DIVA. Their approach handles phylogenetic uncertainty and uncertainty in DIVA optimization. Harris and Xiang (2009) proposed an alternative approach to Bayes-DIVA, which differs in its ability to handle uncertainty at some nodes. We have written Statistical Dispersal-Vicariance Analysis (SDIVA), a program which complements DIVA, implements the methods of Nylander et al. (2008) and Harris and Xiang (2009), and determines statistical support for ancestral range reconstructions using a novel method, the S-DIVA value. In S-DIVA, the frequencies of an ancestral range at a node in ancestral reconstructions are averaged over all trees and each alternative ancestral range at a node is weighted by the frequency of the node occurring or by some other measure of support for the node. S-DIVA is easy-to-install, provides a user-friendly graphical interface, and generates exportable, graphical results (Fig. 1a and b). 2. Description 2.1. Program features The S-DIVA program requires a set of trees from phylogenetic analysis (a ‘‘trees file”), a final representative tree, and range infor- Author's personal copy Y. Yu et al. / Molecular Phylogenetics and Evolution 56 (2010) 848–850 849 Fig. 1. Graphical output from S-DIVA. (a) Graphical results of ancestral distributions for simulated phylogeny with 9 species and 3 areas. A, B and C are ranges of terminals. Pie charts at nodes show probabilities of alternative ancestral ranges; (b) Alternative ancestral ranges of the node of ((4, 9), 2) displayed as a pie chart and bar charts by S-DIVA. The node of terminals 2, 4 and 9 has two possible ancestral ranges ‘‘AB or BC”, the occurrence of each range is AB: 60%, BC: 40%. Probability of this result may be interpreted as 100% since the frequency of occurrence of the node (pn) is 100%; (c–g) Five optimal reconstructions resulting in probabilities in a and b. Numbered nodes (roman numerals) correspond to those in Table 1. Note that node numbers are not part of the S-DIVA output. mation for terminal taxa. Tree file formats generated by the programs BEAST (Drummond and Rambaut, 2006), PAUP* (Swofford, 2003) and MrBayes (Huelsenbeck and Ronquist, 2003) are currently supported by S-DIVA. Range information may be loaded as a comma separated values file or entered directly into S-DIVA through the user interface. S-DIVA allows users a variety of options, which customize analyses for individual needs. Dispersal-Vicariance Analyses in S-DIVA are performed by DIVA 1.2 (Ronquist, 2001). In an S-DIVA analysis with default settings, ancestral reconstructions are performed using DIVA 1.2 for all trees in the trees file. The probability (p) of an ancestral range x at node n on the final P tree is calculated as pðxn Þ ¼ m t¼1 Fðxn Þt pn where t is the selected tree, m is the total number of sampled trees, F(xn)t is the occurrence of an ancestral range x at node n for tree t, and pn is the support for the node. F(xn)t is calculated as the actual frequency of x within the pool of ancestral range reconstructions (Harris and Xiang, 2009): Fðxn Þ ¼ i=Dt . The value i is the number of times the range x occurs in the total number of alternative reconstructions D at node n in Pm tree t. S-DIVA output includes t¼1 Fðxn Þ and the frequency of occurrence of each node of the final tree in the sample of trees. The latter may be interpreted as pn or an estimate of pn and can P thus be multiplied by m t¼1 Fðxn Þ to determine p(xn). Alternatively, other means, independent of S-DIVA, may be used to determine pn. Default settings in S-DIVA generally implement the Bayes-DIVA method described by Nylander et al. (2008) except that i/Dt is used to calculate F(xn) and trees from sources other than Bayesian analysis are allowed (e.g., Micó et al., 2009). The S-DIVA value, SV, of an optimal reconstruction of the final P tree, is calculated as SV ¼ c1 n¼1 Pðxn Þ, where c is the total number of terminal taxa and c 1 is the total number of nodes. The higher the S-DIVA value the greater the probability of a reconstruction (Fig. 1a–g, Table 1). The graphical output of S-DIVA (Fig. 1a and b) is designed for easy visualization and navigation of results with displays for the final tree, each node, and each optimal reconstruction. Graphics are high resolution and may be browsed on-screen or exported as .jpg or .png files. Other options in S-DIVA include: 1. Perform biogeographic analysis for a user-specified lineage with an undefined sister group as in the method of Harris and Xiang (2009) and as an alternative to the Nylander et al. (2008) method. 2. Estimate the probability of optimal ancestral ranges at a single, user-specified node. 3. Add distribution information for an omitted taxon at a userspecified node. 4. Limit analysis to a random sample of trees from the trees file. 5. Exclude the first specified number of trees in the trees file from analysis by setting a burn-in. 6. Apply DIVA options in S-DIVA through graphical user interface and command line formats. S-DIVA has been tested using the simulated dataset of 100 randomly sampled trees from Harris and Xiang (2009). Harris and Xiang (2009) used these trees to estimate the biogeographic histories of four lineages using the Bayes-DIVA method of Nylander et al. (2008) and their own method. Results obtained from S-DIVA were identical to those reported from manual calculations by Harris and Xiang (2009) except for several slight differences observed beyond the second significant digit to the right of the decimal. These differences are probably explained entirely by the greater precision of S-DIVA calculations compared to the manual method of Harris and Xiang (2009) using Microsoft Excel. 2.2. Implementation details The main routine in S-DIVA is written in VB.net and uses the program DIVA 1.2 for handling DIVA analysis. The S-DIVA web site Author's personal copy 850 Y. Yu et al. / Molecular Phylogenetics and Evolution 56 (2010) 848–850 Table 1 Table for optimal reconstructions in Fig. 1c–g. I II III IV V VI VII VIII SV 1 (Fig. 1c) Range (x) V(n) AB 100 AC 100 AB 60 B 80 AB 80 AC 60 A 60 AC 60 – 600 2 (Fig. 1d) Range (x) V(n) AB 100 AC 100 AB 60 B 80 AB 80 BC 40 B 40 BC 40 – 540 3 (Fig. 1e) Range (x) V(n) AB 100 AC 100 AB 60 AB 20 A 20 AC 60 A 60 AC 60 – 480 4 (Fig. 1f) Range (x) V(n) AB 100 AC 100 BC 40 B 80 AB 80 AC 60 A 60 AC 60 – 580 5 (Fig. 1g) Range (x) V(n) AB 100 AC 100 BC 40 B 80 AB 80 BC 40 B 40 BC 40 – 520 Calculations of P(xn) assume that pn for all nodes is equal to 1.0. gives a detailed example illustrating how to use the program. Example files and a user’s manual are provided with the S-DIVA download. A web server is available for running S-DIVA analyses and can be accessed at http://mnh.scu.edu.cn/sdiva_web. The online version of the program offers a full user interface and makes the software accessible to MAC and Linux users. The S-DIVA web service is still in beta and we recommend the offline version of S-DIVA. 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