408.
Change linear order of current Thryothorus
wrens (II)
409.
Recognize genus Pheugopedius (II)
410.
Recognize genus Thryophilus (II)
411.
Recognize genus Cantorchilus (II)
Proposals (408-411) to South American
Classification Committee
Summary: This proposal would result in a new genus name or names for the
current SACC Thryothorus wrens. In Proposal 219,
all committee members were in favour of taking such a step, but there was no
agreement on using Mann et al. (2006)'s three-genus approach for South American
Thryothorus. This decision should be reconsidered in
light of vocal analysis by Mann et al. (2009). However, if the three genus approach is again to be
rejected, then SACC should either revert to Hellmayr's two genus treatment for
S American Thryothorus or move them
to other genera. The current baseline remains as Thryothorus for all these species, which cannot be supported.
Discussion: In Proposal 219, in a
close vote, SACC decided not to split S American Thryothorus into three new genera. However, there was considerable support in the comments of
dissenters for moving all South American Thryothorus
to Pheugopedius. The proposition that Thryothorus is not monophyletic has
strong support from multiple studies, as discussed in Proposal 219 and further
shown by Mann et al. (2006) and papers cited therein, with true Thryothorus occurring only outside the
SACC region.
There was some scepticism over Proposal 219 given that Mann et al.
(2006)'s diagnosis of the new genus Cantorchilus
involved only molecular characters: "Currently, no known uniquely derived morphological characteristics
diagnose the genus Cantorchilus, as defined here. Given current taxonomic and
character sampling, the genus is diagnosable by 9 unreversed synapomorphies in
cytochrome b (including: A150C, A156G, C297T, A876C, C903A, C924A, A948G, C960A
and C1116A, where aNb refers to the ancestral state a and derived state b at
position N), all at third codon positions, including 6 transitions and 3
transversions, one of which results in an amino acid replacement (I372M)."
Daniel Cadena (who voted in favour of adopting the three genera) in his
comments on Proposal 219 noted "it
appears to me that the songs of Thryophilus (rufalbus and nicefori, which I am
familiar with) stand out as rather unique when compared to those of other
"Thryothorus" I know."
This has now been borne out with analysis. Mann et al. (2009), based on sampling of almost all relevant
species, showed the three proposed genera to be diagnosable on the basis of
duetting behaviour and also noted some behavioural differences (separation by
forest strata) between members of different proposed new genera where they
occur together. For example, Thryophilus sensu stricto don't duet or
duet in a very temporally uncoordinated fashion, whereas Cantorchilus show the highest degree of temporal coordination. Van Remsen (who voted in favour of
three genera) noted previously (in summarising the comments of dissenters) that
the "three separate genera … are …
morphologically "below" the traditional level of generic
distinctiveness".
However, Mann et al. (2009) suggest that the three groups are diagnosable
by ecological characters in addition to molecular characters. As a result, the proposed genera are at
least as supportable as some of the N American wrens related to this group.
Given the committee member comments on Proposal 219, changing the genus
for S American Thryothorus would
appear to be unfinished business.
For those that consider the three genus approach still to be weakly
supported, there are two options: (i) reverting to Hellmayr's two genus
treatment, which could be regarded as a status
quo ante when Thryothorus is
properly restricted to N America; or (ii) place all S American Thryothorus in Pheugopedius. In
either of these treatments, the non-recognized genera of Mann et al. (2006)
could be treated as sub-genera. If
the SACC later comes to the conclusion that a greater Pheugopedius is not monophyletic, as suggested by Mann et al.
(2006, 2009), then a further rearrangement could be considered in future, but
this would affect less than half of the species currently recognised in this
group if Pheugopedius is used, or
just two species if SACC reverts to Hellmayr's treatment.
An unfortunate consequence of Proposal 219 being rejected was that the
proposed new linear order was also rejected. Proposal 408 would re-arrange the genus (whatever its name)
so as to reflect the relationships suggested by Mann et al. (2006) and
recommended in Proposal 261, which maintain the existing order generally but rearrange
to show the suggested three (sub-) genera (together with minor tweaks to the
order of the Cantorchilus group),
with "incertae sedis" (within Cantorchilus)
griseus at the end of the order:
Old linear
order |
Proposed new
linear order |
spadix |
(sub-)genus Pheugopedius: spadix (sub-)genus Thryophilus: rufalbus (sub-)genus Cantorchilus: leucopogon |
A positive vote on Proposal 408 would result in this new linear order
being adopted.
As a result of Proposal 219 not passing, all Thryothorus were moved to
Pheugopedius in the Colombian
checklist three years ago (Salaman et al. 2007, 2008, 2009) assuming that SACC
would also do so in due course based on comments of committee members. One of the authors of this proposal has
sought to adopt such an approach in some journal papers including site/regional
checklists and range extensions, but has become somewhat fed up with editors
and peer reviewers commenting that these birds should be Thryothorus due to the SACC's treatment (particularly for the
"core" Pheugopedius that
would be recognised in this genus under Mann et al.'s suggested treatment where
10/10 SACC members supported recognising this genus!). SACC action on this matter would be
welcomed as other persons working with Neotropical birds may have had similar
experiences.
(Another approach would be to merge Henicorhina,
Uropsila, Cinnycerthia, Cyphorhinus and S American Thryothorus into one genus, but that would cause more nomenclatural
instability than it is worth and rob us of some well-defined genera.)
The following votes would have the following results, assuming that
proposal 408 (on linear order) passes:
409 passes,
410 rejected (or 409 and 411 pass but 410 does not): |
409 and 410
pass, 411 does not: |
409, 410 and
411 pass: |
Pheugopedius: spadix |
Pheugopedius: spadix Thryophilus: rufalbus |
Pheugopedius: spadix Thryophilus: rufalbus Cantorchilus: leucopogon |
References:
Mann, N.I.,
et al. 2006. Molecular data delineate four genera of "Thryothorus"
wrens. Mol. Phylogenet. Evol. 40:
750-759. http://www.tc.umn.edu/~barke042/Publications.php
Mann, N.I.,
Dingess, K.A., Barker, F.K., Graves, J.A., Slater, P.J.B. 2009. A comparative
study of song form and duetting in Neotropical Thryothorus wrens. Behaviour 146, 1-43
Recommendations: (From Thomas
Donegan): I would strongly recommend a YES vote to 408 and 409; for votes
410-411, I can see reasons why committee members might vote either way. My own view is that a yes vote is more
sensible in both instances. Mann
et al. (2006, 2009) taken together provide a solid rationale for their
recommendations and have clearly considered the issues at length. Their diagnosis of the three new genera
now has real world as well as molecular support. Given that all the genus names of these species will be
changed anyway, a priori, their treatment
should probably best be followed rather than being second guessed.
(From Keith Barker): I would
strongly recommend a YES vote for all four of these proposals, for the reasons
set out in Mann et al. (2006, 2009).
However, if Cantorchilus is
not to be recognized, I would strongly recommend voting yes on 408-110, taking
us to the status quo ante Hellmayr’s
lumping of all within Thryothorus,
and avoiding placement of taxa into Pheugopedius
that have never been there.
Thomas Donegan & F. Keith
Barker, August 2009
=====================================================
Comments from Stiles:
“408. YES. The new
linear order presented clearly reflects phylogeny better than our current
arrangement.
“409. YES, to
recognize Pheugopedius; the
Neotropical species clearly do not belong in Thryothorus; their inclusion would render this genus polyphyletic.
“From here on, however, things get a bit dicier. The proposal contains
some confusion regarding whether the current practice of lumping all into Thryothorus vs. the “two-genus” approach of recognizing Thryophilus and Pheugopedius
is due to Hellmayr or is “pre-Hellmayr”.
Looking up what Hellmayr actually wrote in “birds of the Americas”
(1934), I find that he indeed lumped all the Neotropical forms (as well as ludovicianus, the only “true” Thryothorus) into a single genus. However, the idea was not original with
him; he was following van Rossem (Trans. San Diego Soc. Nat. Hist. 6, p. 208,
date not given) in stating: “…the
differences between Thryophilus, with
open nostrils, and Pheugopedius, with
partly operculate nasal groove, is so completely bridged by intermediate
species that no dividing line can be drawn. Moreover, the two types of nostrils, used as criteria for
generic distinction, even occur within the same species, the case of T. modestus being very appropriately
cited by van Rossem as a striking example of such variation. If Pheugopedius
and Thryophilus be merged, there
is no valid ground for the retention (sic) of Thryothorus, since a good many species of “Thryophilus” agree with the Carolina Wren in the lesser graduation
of the tail.”
“If these were the only features defining Pheugopedius and Thryophilus,
their lumping would seem to be in order, but Hellmayr did not give diagnoses
for genera. I therefore went to Ridgway (Birds of N. and Middle America, USNM
Bull. 50, vol. 3, 1904) for these.
The following table summarizes the points of difference that I was able
to extract from Ridgway’s diagnoses:
Pheugopedius |
feature |
Thryophilus |
Longitudinal to
fusiform |
Nostril |
Small, round or
oval |
Decumbent
operculum overhangs nostril, posterior end contacting with or overhung by
feathers of nasofrontal antiae |
Operculum |
No operculum, but
a naked membrane may extend along upper edge of nostril, separated from
nasofrontal antiae |
Graduated for 1/3
or more of its length |
Tail |
Graduated for 1/3
or less of its length |
Straight for ≥
½ of its length, abruptly decurved terminally |
Exposed culmen |
Straight to
slightly decurved, gradually decurved terminally |
Slightly concave,
deflexed basally, slight indication of subterminal notch |
Maxillary tomium |
Straight to
slightly decurved terminally with distinct subterminal notch |
Short but
distinct, occasionally 1-2 well developed |
Rictal bristles |
Obvious, 1-3 well
developed |
Short, rounded;
primaries 3-7 or 4-6 longest, 8<<3 |
Wing shape |
Moderate,
rounded; primaries 4-7 longest, 8 variable |
D(igit) 4 w/o
claw reaches to middle of subterminal phalanx of d3, claw reaches base of
claw of d3 |
Length of toes |
D4 w/o claw
reaches subterminal joint of d4, claw does not reach base of claw of d3 |
As a basis for
separating genera, this is cutting it pretty fine, but is fairly typical of
generic diagnoses of Ridgway’s time.
I then went to our collection to check out these characters. Surprisingly, I found that in specimens
in which the nasal area was intact, the difference cited by Ridgway does seem
to hold in most cases. All species
show a naked membrane partly covering the nostrils but in all of the Pheugopedius, this extends from the
dorsal edge of the nasal fossa and does partly cover the nostril –
although in some where the membrane has been pulled back, the nostril appears
more rounded. In Thryophilus, this membrane extends from
the proximal end of the fossa distally to the nostril, which does indeed appear
more rounded – but in a few the dorsal extension is more pronounced,
though never so much as in the Pheugopedius. (We do not have T. modestus here, so I could not check directly van Rossem’s
statement.) The tail is indeed
more graduated in Pheugopedius, but
in some Thryophilus it approaches
pretty closely this degree of graduation.
Regarding the curvature of the culmen, there is much variation within
species: the tendency for a more strongly decurved tip in Pheugopedius holds, but some (young?) individuals show a more
gradual curvature; a few individuals of several species in Thryophilus have more abruptly curved bill tips, though not so
pronounced as in most Pheugopedius. The same goes for the subterminal notch:
though on average it is more pronounced in Thryophilus,
one can find the full range of variation in virtually all species. I did not go into detail regarding wing
shape, but again, primary 3 seems to average relatively longer in Pheugopedius but the difference is
pretty slight. I could see no
consistent difference in the relative length of the toes, and the rictal
bristles seemed to vary more according to preparation than anything else. In conclusion, there is some
morphological basis for recognition of Thryophilus
as distinct from Pheugopedius but
the differences are often slight and bridged by individual variation in many
cases (perhaps related to age for bill shape?). Given that these differences, such as they are, do correlate
with the genetic data, I could be induced to vote a lukewarm YES on proposal
410 to recognize Thryophilus (although
I would not be surprised – or heartbroken - if many SACC members
disagreed with me).
“However,
I could find no morphological character(s) that would convincingly separate Thryophilus (sensu stricto) from Cantorchilus.
I am reluctant to base a genus
on zero morphological differences (but if Keith or Thomas wish to conduct a
more thorough morphological analysis and do find something, I could go along
with it). The song differences are
interesting, but I am also reluctant to use such differences to separate genera
in oscines where song learning is pronounced and local song dialects are
frequent. In species like rufalbus, sometimes one hears perfect
coordination between males and females (the female adding her notes to the end
of the male’s with no discernable break, as in modestus, for example), at other times (especially in minlosi of the Llanos) coordination
seems lacking or less developed.
Hence, I will vote NO on 411, at least for the present, though I am
willing to recognize Cantorchilus as
a subgenus of Thryophilus (or Pheugopedius) based on the
genetics. In passing, I note
that the recognition of species in Scytalopus
is based to a great extent upon song differences that line up with genetic
differences, but here we are dealing at the species, not genus level in a group
in which song learning is presumed to be absent.
“I
also note that no genetic data are available for T. griseus, which is morphologically much more distinctive than
anything in Pheugopedius or Thryophilus with its much shorter and
nearly non-graduated tail and grey coloration (and canopy habitat?). Not having the song paper I don’t know
if its song was included in the pertinent paper of Mann et al., but on the face
of it, it might well be worth looking at (we have a recent specimen here,
Daniel!)”
Comments
from Robbins: “YES. I’m on the fence on this one, as it really doesn’t
bother me that Cantorchilus is
defined primarily by genetics (vocal data are suggestive). The morphological differences between
the Pheugopedius and Thryophilus clades are so slight that if
those were the only data supporting recognition of those two genera then I
would vote no on that proposal.
Thus, in an attempt to be consistent, I vote for the recognizing Cantorchilus, although I’m not totally
convinced that this is the right course of action.”
Comments
from Zimmer: “
“Proposal #408:
Change the linear order of current Thryothorus
wrens. YES, our current
arrangement does not square with the available evidence.
“Proposal
#409: Recognize Pheugopedius. Again, YES, as the evidence is pretty clear that Thryothorus applies only to ludovicianus/albinucha, and that all of
the South American species belong somewhere else.
“Proposal
#410: Recognize Thryophilus. YES, based on the combination of molecular evidence, vocal
evidence (as outlined in Mann et al.
2009), and Gary’s assessment of Ridgway’s diagnosis of Pheugopedius versus Thryophilus.
“Proposal
#411: Recognize Cantorchilus. Gary’s points on this one are well taken. Although there is definite
morphological cohesion between most of the species that would be placed in Cantorchilus (superciliaris, leucotis, longirostris, guarayanus), there is little
if anything in the way of morphological characters that would allow the genus
to be diagnosed relative to Thryophilus. I also share Gary’s hesitance regarding
the use of vocal differences to define a genus of oscine passerines, which can
learn their songs. However, I
think that Mann et al are really on
to something as regards vocal differences in duetting behaviors in these
wrens. When you read through the
list of different singing styles (Table 4 in Mann et al. 2009) it is somewhat confusing because of the sheer
complexity of the vocalizations and duetting behaviors involved. But, if you have field experience with
the species involved, you can see the patterns that Mann et al refer to, and many of the species in each proposed “new”
genus do sort out as having similar singing “styles”. It seems to me that the underpinnings that allow males and
females of one species to frequently engage in highly coordinated, complex,
antiphonal duets, as opposed to those species in which duetting is relatively
rare and/or less coordinated are more likely to be genetically based than are
simple differences in song dialects, which, in this family, can obviously be
learned. We still don’t really
have a handle on what constitutes genus-level vocal distinctions, although I am
reminded of that old quote regarding obscenity – “we can’t really define
it, but we know it when we see it”.
Clearly, there is more work to be done in refining some of Mann et al’s song style categories, and, as
the authors themselves point out, not every species in each proposed genus
displays the same song styles.
However, the authors have provided a good platform for investigating the
extent of the genetic basis for the differences in vocal behavior in these
wrens, and I do think that where there is smoke there is fire.
“Gary raised the
question of T. griseus, which would
seem to be a potential fly-in-the-ointment for any proposed phylogenetic
arrangement, because without DNA we really don’t know where it belongs. Morphologically, it is more different
from all other “Thryothorus” than any
of them are from one another. And
no, Mann et al 2009 did not have
vocal data on griseus in their
paper. However, I find it
interesting that under their proposed arrangement, griseus would be in Cantorchilus,
as would leucopogon and thoracicus (of Central America). I recently published a paper detailing
observations on vocalizations (including duetting behavior), ecology, and
nesting of T. griseus (Zimmer &
Whittaker 2009, Cotinga 31:80-85),
and off the top of my head, I would say that the singing style of griseus would be closest to Style 9 as
defined by Mann et al. (which was
published while our Gray Wren paper was in press), with males having different
categories of song (series of single tonal notes as well as more complex
phrases, both of which are repeated and increase in amplitude through the
course of the song), and duets formed by females joining in with complex
phrases. Mann et al. classified both leucopogon
and thoracicus as Style 9, and I
would strongly agree with that classification. It is also interesting that both leucopogon and thoracicus
show some ecological similarities to griseus,
in that all three species tend to forage mostly in low or mid-level vine
tangles. Molecular analysis may
ultimately show that griseus isn’t
particularly close to any of the other South American “Thryothorus”, but I do find it interesting that ecologically and
vocally, it is closer to thoracicus &
leucopogon, which molecular data would place in Cantorchilus.
“When all is said
and done, I have to vote YES on recognizing Cantorchilus
along with Pheugopedius and Thryophilus, with the recognition that
we may end up moving some of the constituent species between genera as more
molecular and vocal data become available (especially as regards griseus).”
Comments
from Cadena:
“409-411. YES
to all three proposals. I think we made a mistake when considering proposal
219. Back then, the discussion led to rejection of the proposal because
committee members disagreed on whether one should recognize one or three genera
for the South American "Thryothorus".
This implied that we have maintained a genus that has been convincingly shown
not to be monophyletic (owing to the position of ludovicianus).
“When discussing proposal 219, I tried to emphasize
that the three genera proposed by Mann et al., and now endorsed by Donegan and
Barker in these proposals, are strongly supported clades. This suggests that
one cannot go wrong by giving names to these groups. In contrast, support for
the monophyly of a clade formed by all three proposed genera to the exclusion
of other wren genera is nonexistent. Therefore, I contend that recognizing a
broad Pheugopedius is untenable with
the evidence at hand. I would also like to emphasize that even if the three
clades turn out to form a monophyletic group, a classification that ranks each
of them at the genus level would be stable (i.e. monophyly of the group would
not require making any further changes). In contrast, if we adopt a broad Pheugopedius as suggested by committee
members before, and this genus turns out not to be monophyletic (note that the
molecular data point in this direction), we will need to revisit the
classification of the group once again, leading to instability.
“Finally, it is nice to see that there is some
evidence from vocalizations, etc. that aids with the diagnoses of the new
proposed genera. However, I think that this should not be a requirement to
justify changes in situations like this: solid phylogenetic analyses tell us
that our current taxonomy is inconsistent with evolutionary history, so we need
to change it. It would be nice if all named groups had phenotypic diagnoses,
but I believe that it is more important that they represent monophyletic
groups. As Kevin said, we might end up needing to move a few species between genera
as data accrue in the future, but this is fine. Let's act based on what we
already know.”
Comments
from Jaramillo:
“
“Proposal 408.
Change linear order of current Thryothorus wrens (II)
Yes – this appears to better fit molecular, as well as behavioural
data sets.
Proposal 409.
Recognize genus Pheugopedius (II)
Yes – this one is clear based on the data.
Proposal 410.
Recognize genus Thryophilus (II)
Yes – Again, this seems to be the right course
of action based on molecular data, morphology and voice.
Proposal 411.
Recognize genus Cantorchilus (II)
Yes – This was the most problematic one for me.
What I found most helpful were the comments by Gary Stiles and then Kevin
Zimmer in the argument for whether we should recognize a genus based entirely
on molecular characters. The clarification came in how the vocal data is
viewed, and I think that Kevin really hit the nail on the head. The vocal data
is there and they duet and vocalize in a different way, consistently within
each genus, but it is very difficult to describe properly. It is described
awkwardly but in print in the Mann paper, so on the whole I am cautious but
believe that a yes vote is the way to go on this. Voice is incredibly important
in wrens, and in a rather complex manner.”