Shakya, S. B. and Sheldon, F. H. (2017), The phylogeny of the world's bulbuls (Pycnonotidae) inferred using a supermatrix approach. Ibis. Accepted Author Manuscript. doi:10.1111/ibi.12464
[abstract]
Shakya, S. B. and Sheldon, F. H. (2017), The phylogeny of the world's bulbuls (Pycnonotidae) inferred using a supermatrix approach. Ibis. Accepted Author Manuscript. doi:10.1111/ibi.12464
[abstract]
Hypsipetes leucocephalus and Cerasophila thompsoni having near-identical sequences is another thing that may seem a bit improbable.The fine detail some of the Philippine species looks highly dubious to me. The results show Thapsinillas as closer to Hypsipetes guimarasensis than H. philippinus is. This makes no sense morphologically or biogeographically. I also doubt that H. siquijorensis is closer to philippinus than guimarasensis is, though it is less impossible. I suspect there is a problem either with the sequence lengths or the statistics. It would have been nice to see a comparison of H. monticola, H. siquijorensis and H. cinereiceps, and also everetti, haynaldi and catarmanensis too.
Southeast Asia is one of the most geologically dynamic regions of the world with great species diversity and high endemism. We studied the bulbuls of the south and southeast Asian genus Iole (Aves: Pycnonotidae) in order to analyse their evolutionary relationships and describe their patterns of diversification and delimit species boundaries. Our phylogeographic reconstruction, based on two mitochondrial and one nuclear markers, sampled from all 13 recognized Iole taxa, presently grouped as four species, revealing three primary lineages: (1) a Palawan lineage (2) a Sundaic group distributed in the Malay Peninsula, Sumatra and Borneo and (3) an Indochinese group distributed throughout continental Southeast Asia. Divergence time estimation suggested that the Palawan lineage diverged during the Miocene (around 9.7 Mya), a later split between the Sundaic and Indochinese lineages occurring around 7.2 Mya. The present classification of Iole based on morphology does not accurately reflect taxonomic relationships within the genus, in which we recognize five more putative species. An integrative approach that incorporates morphology and bioacoustics should further refine our understanding of species limits among Iole taxa.
Status as species accepted tentatively here, but relationship with P. icterinus, to which it is identical in appearance except for whitish subterminal spots on wing-coverts and remiges, puzzling; recent searches at type locality proved fruitless, and results of ongoing attempts to extract and compare genetic material awaited with interest.
J. Martin Collinson, Martin Päckert, Yvonne Lawrie, Wulf Gatter, Till Töpfer, Ben Phalan & Lincoln Fishpool. Taxonomic status of the Liberian Greenbul Phyllastrephus leucolepis and the conservation importance of the Cavalla Forest, Liberia. Journal of Ornithology, First Online: 12 July 2017.
[pdf]
HBWAlive:
J. Martin Collinson, Martin Päckert, Yvonne Lawrie, Wulf Gatter, Till Töpfer, Ben Phalan & Lincoln Fishpool. Taxonomic status of the Liberian Greenbul Phyllastrephus leucolepis and the conservation importance of the Cavalla Forest, Liberia. Journal of Ornithology, First Online: 12 July 2017.
IOC Updates Diary Oct 23
Post proposed status of Liberian Greenbul as plumage variant of Icterine Greenbul on Updates/PL
The recently described Bare-faced Bulbul Pycnonotus hualon from Lao PDR has a very distinct morphology and habitat (karsts). Mitochondrial and nuclear data from the type material demonstrated that P. hualon is sister to members of the genus Spizixos. To highlight its unique morphology and phylogenetic distinctiveness, we describe a new monotypic genus for the Bare-faced Bulbul.
The Bare-faced Bulbul Pycnonotus hualon Woxvold, Duckworth & Timmins, 2009, was first collected from the small limestone karst outcrop of Pha Lom (16°58′13″N, 105°48′48″E), north-east Savannakhet Province, Lao PDR, in late 2008, following a 1995 sighting of strange bald-looking bulbuls about 185 km away, above the Hinboun plain at the northern end of the Khammouan limestone massif (18°04′N, 104°31′E). As of 2017, the species remains known only from the karst landforms of Lao PDR between the Pha Lom and above the Hinboun plain. This discovery forms part of a sustained pulse of discoveries of new bird and mammal species in and around the Annamite Mountains of Lao PDR and Vietnam, mostly associated with two distinct habitat types, karst limestone and wet evergreen forest. Several of the newly discovered species are phylogenetically highly distinct. These include a forest bovid (Saola Pseudoryx nghetinhensis Vu, Pham, Nguyen, Do, Arctander & MacKinnon, 1993; Vu et al. 1993); the first representative of Caudata for Lao PDR (Lao Warty Newt Laotriton laoensis (Stuart & Papenfuss, 2002); Stuart & Papenfuss 2002); and a living member of the Diatomyidae (Kha-nyou Laonastes aenigmamus Jenkins, Kilpatrick, Robinson & Timmins, 2005; Jenkins et al. 2005), a lineage of rodent formerly presumed to have been extinct for the past 11 million years (Dawson et al. 2006). Here we investigated the phylogenetic relationships of the Bare-faced Bulbul (Fig. 1).
Nok, gen. nov.
Type species: Pycnonotus hualon Woxvold, Duckworth and Timmins, 2009 by original description.
Etymology: Nok means bird in Lao and is used to highlight the range-restricted distribution of the species. Nouns in the Lao language lack gender. Nok is proposed here as a masculine noun.
Fuchs, J., Pasquet, E., Stuart, B. L., Woxvold, I. A., Duckworth, J. W. and Bowie, R. C.K. (), Phylogenetic affinities of the enigmatic Bare-faced Bulbul Pycnonotus hualon with description of a new genus. Ibis. Accepted Author Manuscript. doi:10.1111/ibi.12580
Abstract:
Thus, back then and there, melanocephalus (Latin ending) and melanocephalos (same word, Greek ending) were indeed to be treated as identical.Generic and specific names, spelled alike, or differing in spelling only as indicated below, are to be considered identical (respecting 'emendations,' see Canon XXXI):
[...]
(b) Whether the ending is masculine, feminine, or neuter, or in Greek or Latin form; e. g., Otostomus, Otostoma, and Otostomum; Nettion and Nettium.
Article 58 specifies:57.6. One-letter difference. Except as specified in Article 58, a one-letter difference between species-group names combined with the same generic name is sufficient to prevent homonymy.
melanocephalos and melanocephalus differ by the use of o and u, respectively, as their penultimate letter; this type of difference is not listed in Article 58, thus is sufficient to prevent homonymy as per Article 57.6. If the names are not homonyms under the present Code, there is no way that one can preoccupy the other.Article 58. Variant spellings of species-group names deemed to be identical. Species-group names established for different nominal taxa that differ in spelling only in any of the following respects and that are of the same derivation and meaning are deemed to be homonyms when the nominal taxa they denote are included in the same genus or collective group:
58.1. use of ae, oe or e (e.g. caeruleus, coeruleus, ceruleus);
58.2. use of ei, i or y (e.g. cheiropus, chiropus, chyropus);
58.3. use of i or j for the same Latin letter (e.g. iavanus, javanus; maior, major);
58.4. use of u or v for the same Latin letter (e.g. neura, nevra; miluina, milvina);
58.5. use of c or k for the same letter (e.g. microdon, mikrodon);
58.6. aspiration or non-aspiration of a consonant (e.g. oxyrhynchus, oxyrynchus);
58.7. use of a single or double consonant (e.g. litoralis, littoralis);
58.8. presence or absence of c before t (e.g. auctumnalis, autumnalis);
58.9. use of f or ph (e.g. sulfureus, sulphureus);
58.10. use of ch or c (e.g. chloropterus, cloropterus);
58.11. use of th or t (e.g. thiara, tiara; clathratus, clatratus);
58.12. use of different connecting vowels in compound words (e.g. nigricinctus, nigrocinctus);
58.13. transcription of the semivowel i as y, ei, ej or ij (e.g. guianensis, guyanensis);
58.14. use of -i or -ii, -ae or -iae, -orum or -iorum, -arum or -iarum as the ending in a genitive based on the name of a person or persons, or a place, host or other entity associated with the taxon, or between the elements of a compound species-group name (e.g. smithi, smithii; patchae, patchiae; fasciventris, fasciiventris);
58.15. presence or absence of -i before a suffix or termination (e.g. timorensis, timoriensis; comstockana, comstockiana).
Thus, back then and there, a name appearing on p. 301 of a book was indeed to be given precedence over a name appearing on p. 309.Canon XVII. [Of names published simultaneously in the same book, that shall be taken which stands first in the book, regardless of other considerations. [...]]
The two names were published simultaneously but at different ranks. Should they be homonyms (they are not), Art. 24.1 would apply (NB: excluding Art. 24.2; no First Reviser act is possible): it is the name proposed for a full species (i.e., Lanius melanocephalos) that would automatically take precedence over the name proposed for a variety (Lanius collurio, var. ε melanocephalus). Not the opposite, and irrespective of where they appear in the book.Article 24. Precedence between simultaneously published names, spellings or acts.
24.1. Automatic determination of precedence of names. When homonyms or synonyms are established simultaneously, but proposed at different ranks, in the family group, genus group or species group the name proposed at higher rank takes precedence [Arts. 55.5, 56.3, 57.7].
[...]
24.2. Determination by the First Reviser.
24.2.1. Statement of the Principle of the First Reviser. When the precedence between names or nomenclatural acts cannot be objectively determined, the precedence is fixed by the action of the first author citing in a published work those names or acts and selecting from them; this author is termed the "First Reviser".