Proposal (167) to South American Classification Committee
Recognise
the subfamilies Hydrobatinae and Oceanitinae within the family Hydrobatidae
Background
In the SACC Baseline document, as viewed on March 1, 2005, the
following statement is made:
Many classifications (e.g., Carboneras 1992c) divide the family
into two subfamilies, Hydrobatinae and Oceanitinae, but this classification
follows the AOU (1998) in not recognizing these until corroborated by multiple
independent data sets that mark major, deep branches within the family. Recent
genetic data, however, supports recognition of these two subfamilies
(Penhallurick & Wink 2004).
Proposal
Below we reproduce Figure 2 from Penhallurick and Wink (2004).
This shows a Neighbourhood Joining tree showing a Bootstrap Cladogram (1000
replicates) using Jukes-Cantor as a distance algorithm.
Bootstrap cladogram (1000 replicates) reconstructed with the
Neighbourhood Joining (NJ) method using Jukes Cantor as a distance algorithm.
The Storm-Petrel family, Hydrobatidae, has two basal nodes. One
node, containing taxa from Oceanites oceanica Wilson's
Storm-Petrel to Fregetta tropica Black-bellied Storm-Petrel, has 99%
Bootstrap support. The other, containing taxa from Hydrobates
pelagicus European Storm-Petrel to Oceanodroma castro Band-rumped
Storm-Petrel, has 100% Bootstrap support. This provides strong support for the
division of the Hydrobatidae into two subfamilies: Oceanitinae, comprising taxa
from Oceanites oceanica to Fregetta tropica; and
Hydrobatinae, with taxa from Hydrobates pelagicus to Oceanodroma
castro. (see tree in Penhallurick & Wink -- ask Remsen for pdf if
needed).
|
78 |
79 |
80 |
81 |
82 |
83 |
84 |
85 |
86 |
87 |
88 |
[78] Oceanites oceanicus |
|
0.0541 |
0.0321 |
0.0321 |
0.0348 |
0.0709 |
0.0737 |
0.0781 |
0.0681 |
0.0794 |
0.0681 |
[79] Garrodia nereis |
0.1076 |
|
0.0458 |
0.0430 |
0.0403 |
0.0880 |
0.0880 |
0.0781 |
0.0681 |
0.0794 |
0.0681 |
[80] Pelagodroma marina |
0.0936 |
0.0962 |
|
0.0348 |
0.0403 |
0.0794 |
0.0822 |
0.0907 |
0.0765 |
0.0880 |
0.0822 |
[81] Fregetta grallaria |
0.0927 |
0.0989 |
0.0884 |
|
0.0159 |
0.0652 |
0.0709 |
0.0781 |
0.0681 |
0.0794 |
0.0681 |
[82] Fregetta tropica |
0.0892 |
0.1015 |
0.1076 |
0.0744 |
|
0.0709 |
0.0765 |
0.0844 |
0.0681 |
0.0765 |
0.0851 |
[83] Hydrobates pelagicus |
0.1277 |
0.1409 |
0.1330 |
0.1269 |
0.1312 |
|
0.0159 |
0.0844 |
0.0681 |
0.0765 |
0.0851 |
[84] Halocyptena microsoma |
0.1409 |
0.1505 |
0.1435 |
0.1286 |
0.1382 |
0.1006 |
|
0.0443 |
0.0159 |
0.0403 |
0.0294 |
[85] Thalobata castro |
0.1538 |
0.1615 |
0.1635 |
0.1462 |
0.1490 |
0.1212 |
0.1163 |
|
0.0413 |
0.0657 |
0.0565 |
[86] Hydrobates furcatus |
0.1330 |
0.1435 |
0.1356 |
0.1321 |
0.1339 |
0.0822 |
0.0971 |
0.1173 |
|
0.0267 |
0.0348 |
[87] Cymochorea leucorhoa |
0.1382 |
0.1531 |
0.1479 |
0.1260 |
0.1356 |
0.1067 |
0.1085 |
0.1240 |
0.0989 |
|
0.0485 |
[88] Halocyptena melania |
0.1295 |
0.1505 |
0.1417 |
0.1295 |
0.1347 |
0.1085 |
0.0796 |
0.1346 |
0.1076 |
0.1129 |
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The table above reproduces uncorrected p-distances, based on
complete sequences of the mitochondrial cytochrome-b gene, below
the diagonal, and amino-acid distances, based on the 300 bases within
cytochrome-b involved in the production of amino acids, above the
diagonal.
In terms of the uncorrected p-distances, the within-group mean
distance for taxa within the Oceanitinae is 9.501% (S.D. 0.94). The
within-group mean distance for taxa within the Hydrobatinae is 10.631% (SD
1.55). In contrast, the between-group mean distance is 14.086% (SD 0.98). These
data confirm strongly that we are dealing with two distinct subfamilies.
Recommendation: That the subfamilies Oceanitinae and
Hydrobatinae be recognized with the family Hydrobatidae.
John
Penhallurick, March 2005
Comments from Nores: "SI, los datos moleculares de Penhallurick son muy convincentes, aunque no
veo porque hay que tratar esto ahora. Aunque en los comentarios sobre la
familia Hydrobatidae se habla de estas subfamilias, en la check-list
no aparecen subfamilias. De todos modos, pienso que es valorable la propuesta
de Penhallurick."
Comments from Stiles: "YES. In this case the
genetic data are appropriate to the question and the study seems solid. My only
query is regarding our somewhat nebulous criterion of "several independent
studies" for such cases. Presumably the original division into two
subfamilies was based upon a series of morphological and perhaps other
characters - would this constitute "independent evidence"? Or should
we interpret the criterion of multiple independent studies to pertain
specifically to genetic studies? The implication here is that no single study,
however careful or convincing, would suffice to change the 'status quo'."
Comments from Pacheco: "YES. Considero a proposição positiva, na medida em que
confirma informação prévia sobre as relações intra-familiares. Os
resultados obtidos por Penhallurick & Wink parecem demonstrar a
existência desses dois subgrupos."
Comments from Jaramillo: "YES - I think that the
higher level patterns of relationship noted in Penhallurick and Wink (2004) are
solid. Although, they are pretty much the same patterns noted by Nunn and
Stanley (G. B. Nunn, S. E. Stanley 1998. Body size effects and rates of
cytochrome b evolution in tube-nosed seabirds. Mol. Biol.
Evol. 15: 1360-1371.), but this is not surprising as the two sets of work are
based at least partially on the same data. So to address Gary's question, there
are separate recent works that come to the same conclusion, but they are not
entirely independent. Going back to older work and the initial suggestion that
the Storm Petrels fit into two main groupings will almost certainly be based on
morphological data so that is surely independent data. In general, the southern
group (Oceanitinae) have much longer legs than the northern group."