Cladistic permutation tests for monophyly and nonmonophyly
Cladistic permutation tests for monophyly and nonmonophyly
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DOI:
10.1093/sysbio/40.3.366
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发表时间:
1991-09
影响因子:
6.5
通讯作者:
D. Faith
中科院分区:
文献类型:
--
作者:
D. Faith
Recent work on randomization or permutation tests for cladistic structure (Archie, 1989a, 1989b; Faith, 1990; Faith and Cranston, 1991) has revealed some dramatic cases in which apparently phylogenetically informative data in fact have structure that could easily be matched by chance alone. In these tests a particular null model is used in which each character's states are reassigned randomly to the taxa, so that the resulting randomized data set represents random covariation among the characters. The corresponding null hypothesis is that the observed hierarchical structure could be found for such randomized data. A necessary companion to the randomcharacter-covariation null model is some criterion for evaluating and quantifying hierarchical structure. This measure of structure represents a criterion model that prescribes the manner in which the data are expected to relate to the underlying pattern (Faith and Cranston, 1991). In the examples referred to above, hierarchical structure is measured by the length of the corresponding minimum-length tree (other measures of hierarchical structure have been used in a general version of this test; see Faith [1991]). The choice of the parsimony criterion of cladistics implies that the null hypothesis is evaluated by comparing the observed minimum length to that achieved for many randomized data sets. The proportion of all sets (observed and random) having lengths as short as or shorter than the observed length yields the "cladistic permutation tail probability," or PTP (Faith and Cranston, 1991; the same test was independentlyl proposed by Archie [1989a]). The null hypothesis may be rejected, for example at the usual 0.05 level, if 5% or fewer of the data sets have a length equal to or less than that of the original (PTP < 0.05). One of the initial applications of this test (Faith, 1990) and the reply to it (Thomas et al., 1990) have raised some important points of controversy that will be addressed in this paper. In an earlier paper, Thomas et al. (1989) used 12S ribosomal RNA gene sequence data to explore the relationships among South American and Australian marsupials, addressing longstanding controversies about the relationship of the presumed-extinct thylacine (Thylacinus) to these other taxa. Based on their cladistic analysis of these data, they argued that the thylacine is not an outgroup to the Australian marsupials, and is the sister of the Dasyuridae. However, application of the PTP test showed that this data set, which consisted of only seven phylogenetically informative characters (Table la), did not have significant cladistic structure. Thus, the 12S ribosomal RNA gene sequence data constituted insufficient evidence for the inference of the phylogenetic relationship of the thylacine to these other taxa (Faith, 1990). In their reply, Thomas et al. (1990) argued that although the data set as a whole did not have significant hierarchical structure, this was not directly relevant to their hypothesis of interest, which was represented in their reply as the specific question of the monophyly of thylacines and dasyurids. They claimed that, for the evaluation of such hypotheses of monophyly, the bootstrap (Felsenstein, 1985) was a more powerful test (see also Archie, 1989a). Application of the bootstrap test revealed significant support for their hypothesis of