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Pauxi

Cladus: Eukaryota
Supergroup: Opisthokonta
Regnum: Animalia
Subregnum: Eumetazoa
Cladus: Bilateria
Cladus: Nephrozoa
Cladus: Deuterostomia
Phylum: Chordata
Subphylum: Vertebrata
Infraphylum: Gnathostomata
Superclassis: Tetrapoda
Classis: Aves
Subclassis: Carinatae
Infraclassis: Neornithes
Parvclassis: Neognathae
Ordo: Galliformes
Familia: Cracidae
Genus: Pauxi
Species: P. pauxi - P. unicornis

Name

Pauxi Temminck, 1813

Reference

Histoire naturelle générale des pigeons et des gallinaces. 2 p.456,465

The genus Pauxi consist of the two species of helmeted curassows, terrestrial black fowl with ornamental casque on their heads. Both are found in South America.

This genus contains only 2 species, namely

* Northern Helmeted Curassow or simply Helmeted Curassow, Pauxi pauxi
* Southern Helmeted Curassow or Horned Curassow, Pauxi unicornis

The latter was formerly united with in P. pauxi under the name "Helmeted Curassow". It is preferable to use the "Northern" and "Southern" names, because each species contains 2 subspecies, of which one has a round, "helmet-like", and the other an elongated "horn-like" bill knob.

As indicated by analysis of mt and nDNA sequences and calibrated with geological data, this genus' ancestors probably diverged from those of Mitu, their closest living relatives, in the Tortonian (early Late Miocene), some 8-7.4 mya. How the present distribution in 4 small areas quite distant from each other came to be is not known. Given that helmeted curassows are birds of the foothills and uplands, it might be that the ancestral Pauxi population became fragmented by the uplift of the Andes, which in their area of distribution took place during the Late Miocene, around the Pauxi-Mitu divergence and some time after.(Pereira & Baker 2002, Pereira et al. 2002).

Pereira & Baker (2002) reported an interesting find: in the mtDNA phylogeny, Pauxi was paraphyletic, with P. unicornis being resolved as the sister species of Mitu tuberosa. This, of course, does not automatically imply that they are closely related or that the genera are invalid. Rather, the authors point out, given the distinct and peculiar morphology of the two genera, incomplete lineage sorting or hybridization between ancestral individuals of the two species is a more likely explanation. According to their data, there must have been some extent of gene flow between Mitu tuberosa and P. unicornis around 2 mya. Unfortunately, the authors do not provide subspecific identification of their single P. unicornis specimen. In any case, they took care to exclude captive hybridization in their choice of samples, as it is frequently known to occur in curassows and would have confounded the analysis. Altogether, what can be said with certainty is that there seems to have been some extent of hybridization between at least one population of the Southern Helmeted Curassow and female Razor-billed Curassows at the end of the Pliocene.

References

* Pereira, Sérgio Luiz & Baker, Allan J. (2004): Vicariant speciation of curassows (Aves, Cracidae): a hypothesis based on mitochondrial DNA phylogeny. Auk 121(3): 682-694. [English with Spanish abstract] DOI:10.1642/0004-8038(2004)121[0682:VSOCAC]2.0.CO;2 HTML abstract HTML fulltext without images

* Pereira, Sérgio Luiz; Baker, Allan J.& Wajntal, Anita (2002): Combined nuclear and mitochondrial DNA sequences resolve generic relationships within the Cracidae (Galliformes, Aves). Systematic Biology 51(6): 946-958. doi:10.1080/10635150290102519 PDF fulltext

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