Certhioidea

Passerines

Tyranni: Suboscines

Passeri: Oscines

Passerida

Sylvioidea
Muscicapoidea and allies
Passeroidea

The 46 Orders

Paleognathae

Galloanserae

Columbea

Otidae

Gruae

Ardeae

Telluraves

Afroaves

Australaves

Certhioidea tree
Click for genus-level
Certhioidea tree

The new superfamily Certhioidea may be sister to the Muscicapoidea and may even be best treated as part of Muscicapoidea. For now, it is not really clear how the various groups that seem allied to Muscicapoidea fit together. Until this is clarified, I prefer to consider Certhioidea an independent superfamily within Passerida, but closely allied with Muscicapoidea. This all has only minor effects on the linear order, but it does affect the shape of the tree.

Following HBW, I've put the wallcreeper in a separate family. The rest is fairly solid, including the position of the nuthatches, and treatment of gnatcatchers and wrens are sister families.

I've placed Salpornis with the nuthatches instead of the creepers based on Johansson et al. (2008b). Although their results were mixed, and one gene suggested a close relationship to the creepers, Salpornis shares an insertion in β-fibrinogen with nuthatches, gnatcatchers, and wrens that the creepers do not have. This supports the arrangement here with the creepers basal in Certhioidea. As Tietze and Martens (2010) note, there are also morphological reasons to group Salpornis with the nuthatches rather than treecreepers. The treecreepers all have stiffened retrices. Nuthatches, Salpornis and the wallcreper do not.

Price et al. (2014) provided genetic evidence that Tichodromidae and Sittidae are ancient sister taxa. Selvatti et al. (2015) obtained a somewhat different arrangement, with Tichodromidae sister to Certhiidae. However, they relied on only two genes for Tichodroma, whereas Price et al. (2014) used 6 genes. In either case, the division between Tichodroma and its sister group is comparable to the separation between other families in Certhioidea, justifying treatment of Tichodromidae as a family. Further, in view of Selvatti et al., we are not entirely certain that the nuthatches are the wallcreeper's closest relatives.

Tichodromidae: Wallcreeper Swainson, 1827

1 genus, 1 species HBW-13

The family name is sometimes spelled Tichodromididae. It was originally established as the subfamily Tichodromia by Swainson, 1827 (Swainson did not use modern subfamily endings).

Sittidae: Nuthatches Lesson, 1828

2 genera, 30 species HBW-13

Based on Tietze and Martens (2010), the Spotted Creeper has been split into African Spotted-Creeper, Salpornis salvadori, and Indian Spotted-Creeper, Salpornis spilonotus, with the subspecies allocated according to geography.

The arrangement of the nuthatches is based on Pasquet et al. (2014).

White-breasted Nuthatches

I have not adopted the proposed split of the White-breasted Nuthatch, Sitta carolinensis (for details, see Mlodinow, 2014; Spellman and Klicka, 2007; Walstrom et al., 2012). It does deserve some discussion. Spellman and Klicka (2007) found 4 subspecies groups which they referred to as the Eastern; Pacific; Eastern Sierra Nevada (ESN); and Rocky Mountain, Great Basin, and Mexico (RGM) clades. Various subspecies are recognized by various authorities. I will use a relatively expansive version here to cover all the bases.

The Eastern clade (carolinensis group) is resident east of the Great Plains of North America, and includes cookei, litorea, carolinensis, and presumably the possibly extinct atkinsi. The Pacific clade (aculeata group) includes aculeata and presumably alexandrae. The ESN clade (tenuissima group) consists of tenuissima and the northern part of nelsoni. The dividing line between the northern nelsoni and true nelsoni seems to go though the center of Colorado. The birds of the northern Rockies formerly considered part of nelsoni could use a new subspecies name. Finally, the RGM clade (lagunae group) includes, lagunae, true nelsoni, uintaensis, mexicana, and umbrosa. It likely also includes oberholseri and kinneari, although they don't seem to have been sampled. You should not trust the range maps in either Spellman and Klicka (2007) or Walstrom et al. (2012). For example, the type locality for uintaensis (Green Lake, Utah) is not considered part of the range of the WHite-breasted Nuthatch by Walstrom et al. (2012), while neither Walstrom et al., nor Spellman and Klicka show the type locality for oberholseri (Boot Spring, Big Bend, Texas). This got me curious, and I checked eBird. The eBird maps are enlightening here, particularly if you zoom in along the contact zones between the clades.

As is well-known, the 4 clades fall into three call groups: Pacific, ESN/RGM, and Eastern. Spellman and Klicka found relatively deep divisions (up to 3.4 million years) between the three call groups, which a more recent divergence between the ESN and RGM groups. Each of these call groups is a candidate for elevation to species status. Contra Mlodinow (2014), the 3rd edition (1910) of the AOU checklist did not use the name Carolina Nuthatch for carolensis either as a species or subspecies. Nonetheless, it is a fitting name, and does have some history behind it (e.g. Coues, 1903). Slender-billed Nuthatch has traditionally been used for aculeata and can be applied to the Pacific group.

As far as the scientific name of the ESN/RGM group, is concerned, lagunae has priority, and contrary to what one of the NACC committee members thought, has been sampled by Spellman and Klicka (2007). The English name opens up a huge can of worms. Various names have been applied to the various subspecies. These include: San Lucas Nuthatch (lagunae), Rocky Mountain Nuthatch (nelsoni), Inyo Nuthatch (tenuissima), Chisos Nuthatch (oberholseri), Mexican Nuthatch (), Sierra Madre Nuthatch (umbrosa), and Southern White-breasted Nuthatch (kinneari). Although Rocky Mountain Nuthatch has been suggested, much of the range is outside the Rockies, in the Sierra Nevadas, the Sierra Madres, the Chisos, and others. I think Cordilleran Nuthatch would be an appropriate name.

So why not accept the split? Right now, there just isn't enough evidence. Walstrom et al. (2012) considered more genes, and revised the topology, with Carolina basal and Pacific and Cordilleran sister. They also found much shorter divergence dates. Their point estimate was about 550,000 ago for the basal split. This is recent enough to consider them all one species. However, as one of the NACC committee members discussed, aculeata and tenuissima come close to one another in the Sierra Nevadas, being separated by habitat and elevation. There's no hint of interbreeding, but it really hasn't been studied that closely.

The White-breasted Nuthatch may be three species, but as the NACC committee decided, the contact zones need closer study to establish it. The genetics just don't cut it here. Worse, the contact areas seem much more extensive than the NACC appeared to realize. I agree with committee on this one.

Certhiidae: Treecreepers Leach, 1820

1 genus, 9 species HBW-13

The arrangement of Treecreepers follows Päckert et al. (2012b).

Certhiidae tree

Polioptilidae: Gnatcatchers, Gnatwrens Baird, 1858

3 genera, 18 species HBW-12

The Rio Negro Gnatcatcher, Polioptila facilis, and Para Gnatcatcher, Polioptila paraensis, are split from the Guianan Gnatcatcher, Polioptila guianensis. Also, the newly described Inambari Gantcatcher, Polioptila attenboroughi, is added to the list. See Whitney and Alonso (2005) and Whittaker et al. (2013).

Troglodytidae: Wrens Swainson, 1831

20 genera, 87 species HBW-10

Except for Nannus, the wrens are confined to the Americas, where they are present pretty much everywhere south of the northern treeline. The overall arrangement is based on combined cytochrome b and β-fibrinogen analyses of Barker (2004) and Mann et al. (2006). Using only the cytochrome b gene leads to a rather different arrangement. I treat the three major clades as subfamilies: Salpinctinae, Troglodytinae, and Thryothorinae. It is not entirely certain whether Salpinctinae or Troglodytinae is the basal subfamily. I also have rather low confidence in the arrangement within Thryothorinae. The combined data indicate two major clades within Thryothorinae, but the details are somewhat shaky.

Following the taxonomic suggestions of Mann et al., I break Thryothorus into 4 genera: Thryothorus, Pheugopedius, Thryophilus, and Cantorchilus. The SACC failed to pass this, voting 4-4. The discussion indicates that a vote to split the narrow Thryothorus from the rest would have passed. It is clear that the core of Thryothorus does not belong with the rest and must be split. However, a two-way split leaves a broad Pheugopedius that is probably not monophyletic, so I have decided to go with the 4-way split. It is uncertain where the Gray Wren, Cantorchilus griseus, actually belongs. It may end up in a separate genus.

The wrens currently seem to be somewhat overlumped. The arrangement here includes several species that are not currently recognized by either of the AOU committees, although some are recognized in HBW-10 (Kroodsma and Brewer, 2005). The splits that go beyond any of these involve the Winter Wren, Troglodytes troglodytes. Based on Drovetski et al. (2004a) and Toews and Irwin (2008), I've split it into 3 species: Pacific Wren, Winter Wren, and Eurasian Wren. These are placed in a new genus, Nannus. The Winter Wren, Nannus hiemalis, includes the subspecies hiemalis and pullus. The other North American subspecies are included in Pacific Wren, Nannus pacificus. Drovetski et al. included several Aleutian wrens in their analysis, and found that they grouped tightly with pacificus. I am presuming that all of the western subspecies will be close to pacificus. Toews and Irwin studied pacificus and hiemalis where their ranges overlap slightly along the northern British Columbia/Alberta boundary. They found evidence of a high degree of reproductive isolation, which prompts the split here. The eurasian races have not been as closely studies. Drovetski et al. found they form a monophyletic clade sister to Nannus hiemalis. Further, they found there are at least four separate clades that may deserve species rank: troglodytes/indigenus, hyrcanus, nipalensis, and fumigatus/dauricus. As you can see, many eurasian subspecies were not included. I prefer to wait for more information before further splitting the Eurasian Wren.

Among the Troglodytes house wrens I recognize several non-AOU species that Kroodsma and Brewer (2005) also split. Thus we have the North American Northern House Wren, Troglodytes aedon; the Mexican Brown-throated Wren, Troglodytes brunneicollis (which ranges into the mountains of SE Arizona); Cozumel Wren, Troglodytes beani; the Falklands endemic Cobb's Wren, Troglodytes cobbi, which the SACC is again considering recognizing; and the South and Central American Southern House Wren, Troglodytes musculus. Exactly how these all relate is not clear, and whether they truly deserve species status remains unclear (see Brumfield and Capparella, 1996; Rice et al., 1999; Martínez Gómez et al., 2005; Campagna et al., 2012). It has been argued that Antillean races of the Southern House Wren also deserve species rank.

I have followed Vázquez-Miranda et al. (2009) in splitting Rufous-backed Wren, Campylorhynchus capistratus, and Sclater's Wren, Campylorhynchus humilis, from Rufous-naped Wren, Campylorhynchus rufinucha. Although the IOC recognizes this split, the AOU NACC does not. C. capistratus includes nigricaudatus, and presumably xerophilum, nicaraguae, and castaneus. Vázquez-Miranda et al. also found that some of the subspecies of zonatus do not actually belong there, but further study is required to untangle that situation.

Kroodsma and Brewer (2005) include two more splits that I have not followed, splitting White-browed Wren, Thryothorus albinucha, from Carolina Wren, Thryothorus ludovicianus, and splitting Canebrake Wren, Cantorchilus zeledoni, from Plain Wren, Cantorchilus modestus. Although Mann et al. (2006) provide some supporting evidence for both splits, they do not recommend them at this time. In such cases, I generally follow AOU, and will do so here. Gonzalez et al. (2003) analyzed DNA from the Bay Wren, Cantorchilus nigricapillus. They found two major groupings, which could be split into Bay Wren, Cantorchilus castaneus (including odicus, reditus, and costaricensis), and the Black-capped Wren, Cantorchilus nigricapillus (including schottii and connectens).

Lara et al. (2012) announced the discovery of the Antioquia Wren, Thryophilus sernai. Their analysis also suggests that the Rufous-and-white Wren may contain two or more species, but I'd like to see more information on this before making further changes.

Possible splits not followed include three in Cistothorus. The eastern and western Marsh Wrens, Cistothorus palustris, are vocally quite different. The same can be said about the northern and southern Sedge Wrens, Cistothorus platensis, where it is not clear exactly how many species are involved or what their limits are. This uncertainty is why they are treated as a single species. Finally, Apolinar's Wren, Cistothorus apolinari, may include two geographically separated species.

Finally, two of the Henicorhina Wood-Wrens are also candidates for future splits (Dingle et al., 2006, 2008, 2010). The White-breasted Wood-Wren, Henicorhina leucosticta, includes Andean, Chocó, and Central American groups, each of which may deserve species status. The Chocó (inornata) group appears to be more closely related to the Bar-winged Wood-Wren, Henicorhina leucoptera (Dingle et al., 2006). In this list, we currently consider it a subspecies of H. leucoptera.

Dingle et al. (2006) also found that the Gray-breasted Wood-Wren, Henicorhina leucophrys, includes at least 3 clades which might be better considered as species (Central American, Chocó, and Peruvian and Ecuadorian Andes). Caro et al. (2013) focused on the Gray-breasted Wood-Wrens in the Sierra Nevada de Santa Marta of Colombia. The found an altitudial separation in the Santa Martas with a contact zone at about 2270 meters elevation. The highland birds, Santa Marta Wood-Wren (subspecies anachoreta) seem more closely related to the Gray-breasted Wood-Wrens in the Peruvian and Ecuadorian Andes, while the lowland birds, Bangs's Wood-Wren (subspecies bangsi) are more closely related to Gray-breasted Wood-wrens in Venezuela and Colombia. Caro et al.'s analysis suggests there may be additional taxa in this complex worth considering for species status.

Salpinctinae Informal

Troglodytinae Swainson, 1831

Thryothorinae des Murs, 1860 (1852)

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