Abstract
1 min readGenetic sequence data have become widely used in evaluating the unique relationship between geography and evolutionary history for conservation of species. Traditional methods, such as bifurcating trees and Wright's F-statistics, often fall short in detailing past and contemporary events and contribute little intraspecific information (Posada and Crandall 2001; Pearse and Crandall 2004). Phylogenetic techniques, when applied in lower level systematic studies, show poor resolution, often resulting in polytomies and ambiguous connections (Crandall et al. 1994). This is particularly the case when species have recently diverged or have complicated metapopulation structure, in which case, bifurcating trees do not have the ability to accurately depict their evolutionary history (Posada and Crandall 2001). Despite this lack of resolution, broad geographic patterns can still be elucidated for older taxa using phylogenetic approaches. The field of phylogeography began by overlaying phylogenies onto geography and making broad inferences about evolutionary histories of species and populations (Avise 1989). This approach, however, does not provide the opportunity to (1) statistically test the null hypothesis of no geographic association between populations, (2) test whether samples (number of individuals and collection localities) are sufficient, or (3) infer historical and contemporary processes and patterns that dictate current genetic variation (Carbone and Kohn 2004). However, approaches such as Nested Clade Analysis (NCA: Templeton et al. 1995), also known as Nested Clade Phylogeographic Analysis or NCPA (Templeton 2004), provide a statistical framework in which to test hypotheses about historical events and current population structure within species.
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