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Bayesian topology corroborated the morphological hypothesis of the Coronator Group as monophyletic lineage within the subgenus Culex.
Without complete taxonomic sampling at the family level, it is difficult to compare Kim's [ 22] morphological hypothesis of anopluran relationships to the molecular phylogeny.
The topology within this sub-clade differs from the morphological hypothesis of Arnold (1980) [ 34], which supported the following relationship: (S. grandiceps (S. affinis (S. slevini (S. leptocosymbotes, S. doriae)))).
In Crambidae, relationships of the five (of 14) subfamilies sampled were also strongly resolved, corresponding well to the morphological hypothesis of Yoshiyasu [ 67], less well to that of Solis and Maes [ 16].
We synthesized the character sets of Richter & Scholtz (2001) and Poore (2005) [ 3, 4] with those of previous works [ 4, 8, 9, 16] as well as newly published information to derive a revised morphological hypothesis of malacostracan phylogeny.
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The TSPY sequences were subjected to parsimony analyses in PAUP 4.0, followed by tree comparison tests designed to assess existing morphological hypotheses of cercopithecine evolution.
Our trees show broad concordance with previous morphological hypotheses of ditrysian phylogeny, although most relationships among superfamilies are weakly supported.
It would be informative to revisit the morphological hypothesis within the context of the results arrived at herein.
The rejection of the traditional morphological hypothesis is therefore very strong.
Based on the low congruence with morphological hypotheses and lack of significantly better fit than the single-threshold model (see above), we refer only to single-threshold results hereafter.
This highlights that molecular studies based on a single marker can easily yield erroneous conclusions, especially when a priori morphological hypotheses hinder the objective analysis of the molecular data at hand.
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