Summary1. It is widely recognized that macroecological patterns are not independent of the evolution of the lineages involved in generating these patterns. While many researchers have begun to evaluate the effect of ancestordescendant relationships on observed patterns using the phylogenetic comparative method, most macroecological studies only utilize the cross-sectional comparative method to 'remove the phylogenetic history', without considering the option of evaluating its effect without removing it. 2. Currently, most researchers use this method without explicitly evaluating three fundamental evolutionary assumptions of the comparative method: (i) that the phylogeny is constructed without error (which implies evaluating phylogenetic uncertainty); (ii) that more closely related species tend to show more similar characters than expected by chance (which implies evaluating the phylogenetic signal) and; (iii) that the model of the characters' evolution effectively recapitulates their history (which implies comparing the fit of several evolutionary models and evaluating the uncertainty of the estimating model parameters). 3. Macroecological studies will benefit from the use of the comparative method to assess the effect of phylogenetic history without removing its effect. The comparative method will also allow for the simultaneous analysis of trait evolution and its impact on diversification rates; it is important to evaluate these processes together because they are not independent. In addition, explicit evaluations of the assumptions of comparative methods using Bayesian inferences will allow researchers to quantify the uncertainty of specific evolutionary hypotheses accounting for observed macroecological patterns. 4. We illustrate the usefulness of the method using the phylogeny of the genus Sebastes (Pisces: Scorpaeniformes), together with data on the body size-latitudinal range relationship to estimate the effect of phylogenetic history on the observed macroecological pattern.
Sequences from two mitochondrial genes (cytochrome b and NADH1) were used to produce a molecular phylogeny for 12 named and two undescribed species of the genus Oligoryzomys. All analyses placed Oligoryzomys microtis as the most basal taxon, a finding consistent with previous studies that suggested the west-central Amazon as a centre of origin for the tribe Oryzomyini to which Oligoryzomys belongs. Biogeographically, this suggests that Oligoryzomys had a South American origin, and later advanced northwards, entering Central America and Mexico more recently. Different analyses have provided consistent support for several additional clades that did not necessarily agree with the species groups hypothesized by previous studies. A molecular clock derived for these data suggests an origin for the genus of 6.67 Mya, with most speciation within the genus occurring between 3.7 and 1.5 Mya.
The mouse opossums of the genus Thylamys constitute a group of species mainly adapted to open xeric‐like habitats and restricted to the southern portion of South America. We used molecular data (mitochondrial and nuclear sequences) to evaluate the phylogenetic and biogeographical relationships of all currently known living species of the genus, recognizing a new taxon from the middle and high elevations of the Peruvian Andes and evaluating the phylogenetic structuring within T. pallidior and T. elegans, as well as the validity of T. sponsorius, T. cinderella and T. tatei, and the haplogroups recognized within T. pusillus. Our results confirm the monophyly of the genus and that the Caatinga and the Cerrado inhabitants Thylamys karimii and T. velutinus are the most basal species in the radiation of Thylamys. We also calibrated a molecular clock which hypothesized a time of origin of the genus of about 24 My, with most species differentiating in middle and late Miocene and Plio‐Pleistocene times of South America.
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