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RE: New paper on Neoaves



Christopher Taylor wrote:

The genes used for the tree are c-myc, RAG-1, myoglobin, beta-fibrinogen and ornithine decarboxylase - 5007bp in total - under Bayesian analysis.

From the article:

"In concordance with other recent analyses (Sibley & Ahlquist 1990; Cracraft et al. 2004; Fain & Houde 2004), our data recover a clade (figure 1, node 4) that includes the secretarybird and accipitrid diurnal birds of prey (osprey, hawks and allies) to the exclusion of falcons. This grouping is recovered in separate analyses of four of the five investigated genes. The New World vultures clearly have their affinity with other raptors and not with storks (contra, e.g. Sibley & Ahlquist 1990)."


One question to keep in mind is: Do the analyses that incorporate single gene regions yield the same or similar topology as the combined dataset, but with less support; or do they yield a very different topology to the combined dataset tree, with strong support? In other words, does the tree based on a combined dataset (=5007 bp drawn from five different gene regions) improve the resolution of each of the single-gene trees, or does it contradict these single-gene trees? I'd hate to think that there is a belief that you can 'improve' the phylogenetic signal simply by expanding the dataset (=stringing together more and more DNA sequences).

Also, are each of the single-gene trees consistent? Individual gene regions may be better at capturing divergence at a certain level, which means that you're going to get a very muddled phylogenetic signal if you simply string these genes together.

The Anomalogonatae divides basally into two clades whose composition is a bit of a surprise - the one containing Passeriformes, Psittaciformes, Falconidae and Cariamidae, while the other contains Accipitres, Coraciiformes, Piciformes, Bucerotidae, Upupiformes, Trogonidae, Coliidae, Strigiformes, Cathartidae and _Leptosomus_.

I'm not ready to give up on a monophyletic Falconiformes quite yet. I'm also a little suspicious of the fact that the analysis failed to recover a monophyletic Palaeognathae, based on _Apteryx_ and _Rhea_. Perhaps greater sampling of the palaeognaths could have solved this; but this begs the question, how many other clades were not recovered because of inadequate taxon sampling? As a general principle, does increased taxon sampling even help? I'm not certain it does. If a gene is unable to capture the phylogenetic signal, or the analysis is unable to tease out this signal, no amount of taxa will improve the situation.


Cheers

Tim