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The Weights and Measures Commission would, in 1799, adopt a flattening of based on analysis by Pierre-Simon Laplace who combined the arc of Peru and the data of the meridian arc of Delambre and Méchain. [35] Combining these two data sets Laplace succeeded to estimate the flattening anew and was happy to find the suitable value 1 / 334 .
Analyses trait evolution among groups of species for which a phylogeny or sample of phylogenies is available: Trait analysis: M. Pagel, A. Meade BEAST [10] Bayesian Evolutionary Analysis Sampling Trees: Bayesian inference, relaxed molecular clock, demographic history: A. J. Drummond, M. A. Suchard, D Xie & A. Rambaut BioNumerics
By expressing models in terms of the instantaneous rates of change we can avoid estimating a large numbers of parameters for each branch on a phylogenetic tree (or each comparison if the analysis involves many pairwise sequence comparisons). The models described on this page describe the evolution of a single site within a set of sequences.
Incomplete lineage sorting is a common feature in viral phylodynamics, where the phylogeny represented by transmission of a disease from one person to the next, which is to say the population level tree, often doesn't correspond to the tree created from a genetic analysis due to the population bottlenecks that are an inherent feature of viral ...
Mosaic evolution – Evolution of characters at various rates both within and between species; Parallel evolution – Similar evolution in distinct species; Quantum evolution – Evolution where transitional forms are particularly unstable and do not last long; Recurrent evolution – The repeated evolution of a particular character
Cladistic representation of the Mayan linguistic family, going back 4000 years.(The numbers represent proposed historical dates in the Common Era).. In historical linguistics, the tree model (also Stammbaum, genetic, or cladistic model) is a model of the evolution of languages analogous to the concept of a family tree, particularly a phylogenetic tree in the biological evolution of species.
For example, among genera of Cretaceous molluscs, an increase in size is no more common than stasis or a decrease. [15] In many cases, Cope's rule only operates at certain taxonomic levels (for example, an order may obey Cope's rule, while its constituent families do not), or more generally, it may apply to only some clades of a taxon. [18]
The model and implementation of this method can be applied to any species tree. As an example, the species tree of the great apes: humans (H), chimpanzees (C), gorillas (G) and orangutans (O) is considered. The topology of the species tree, (((HC)G)O)), is assumed known and fixed in the analysis (Figure 1). [1]