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Siskins - 1 genus or 3? (1 Viewer)

Acanthis

Well-known member
I see the AOU have a pending proposal for the splitting of the Siskin genus Spinus into 3 genera.

See http://www.aou.org/committees/nacc/proposals/2008-C.pdf

The proposal is as follows:

"Spinus Koch, 1816, for spinus, pinus, dominicensis, and atriceps;
Astragalinus Cabanis, 1851, for tristis, psaltria, and lawrencei; and
Pyrrhomitris Bonaparte, 1850, for the rest of Cental and South American species"

Instead of Astragalinus and Pyrrhomitris the "Taxonomy in Flux" list based on the forthcoming Nguembock et al (2009) paper, uses Pseudomitris and Sporagra respectively.
A brief search through the Richmond Index on zoonomen.net would suggest that the first two mentioned would have priority.
Anyone care to comment? Laurent?

My main reason for posting though is because I wonder if this proposed generic split is really necessary. The 3 groups of Spinus form a fairly well-supported clade in for example:

Arnaiz-Villena (et al) (2007b), Bayesian phylogeny of Fringillinae birds: status of the singular African oriole finch Linurgus olivaceus and evolution and heterogeneity of the genus Carpodacus, Acta Zool. Sinica 53, 826-834.
Arnaiz-Villena (et al) (2008), Mitochondrial DNA Phylogenetic Definition of a Group of ‘Arid-Zone’ Carduelini Finches, Open Ornith. J. 1, 1-7.

And beyond the science, most species are either capped or have black heads and most important of all sound like "a siskin". The have a common, for want of a better word... "Siskinicity". In short if it looks and sounds like a siskin then it's a siskin.

IMO the size of a genus should not be good enough reason to split it. The plausible theory behind the large number of Spinus species is that an invading ancestor found a vacant niche in S. and C. America for a small, agile seedeater and ran with it.

All that being said the American Goldfinches are a little distinct in plumage so if a split is to be made then perhaps Spinus / Astragalinus is warranted.

BTW before anyone asks I don't yet have a copy of Nguembock (2009) and would dearly love to read it. So if anyone has a pdf......
 
No pdf, but a quick glance on John Boyd's TiF Checklist, Spinus is well away from his Pseudomitris and Sporagra, grouping with Acanthis+Loxia. This group is sister to a clade containing Carduelis (European Goldfinch and the Citril finches), Serinus (the Canary and a few others), Pseudomitris and Sporagra (the last two are sisters).

But I have to agree with you that there certainly is a "siskinicity" to Spinus+Sporagra+Pseudomitris!
 
No pdf, but a quick glance on John Boyd's TiF Checklist, Spinus is well away from his Pseudomitris and Sporagra, grouping with Acanthis+Loxia. This group is sister to a clade containing Carduelis (European Goldfinch and the Citril finches), Serinus (the Canary and a few others), Pseudomitris and Sporagra (the last two are sisters).

But I have to agree with you that there certainly is a "siskinicity" to Spinus+Sporagra+Pseudomitris!


I hesitate to bring up anything to do with aviculture here on BirdForums but bird keepers who indulge in the dubious practice of inducing hybridisation in captive finches can tell you that certain pairings will produce fertile young, and others won't. All the greenfinches when crossed produce fertile young and so do combinations of Eurasian Siskin and Hooded, Red and Yellow-faced Siskins.
Many other pairings of Carduelis/Serinus types don't or are only fertile when back-crossed with one of the parent species.

Not very scientific I know but it does suggest that the 'Pine' Siskin and 'South American' Siskin groups at least are very closely related.
 
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... on John Boyd's TiF Checklist, Spinus is well away from his Pseudomitris and Sporagra, grouping with Acanthis+Loxia. This group is sister to a clade containing Carduelis (European Goldfinch and the Citril finches), Serinus (the Canary and a few others), Pseudomitris and Sporagra (the last two are sisters).

But in the attached tree, for instance, the South-American birds look closer to spinus & pinus than to tristis, psaltria & lawrencei.

:eek!:
 

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I hesitate to bring up anything to do with aviculture here on BirdForums but bird keepers who indulge in the dubious practice of inducing hybridisation in captive finches can tell you that certain pairings will produce fertile young, and others won't. All the greenfinches when crossed produce fertile young and so do combinations of Eurasian Siskin and Hooded, Red and Yellow-faced Siskins.
Many other pairings of Carduelis/Serinus types don't or are only fertile when back-crossed with one of the parent species.

Not very scientific I know but it does suggest that the 'Pine' Siskin and 'South American' Siskin groups at least are very closely related.
This is true. Red factor Canaries were produced by pairing Canaries with Red Hooded Siskins. These were then backcrossed with Canaries until about eh fourth generation they were structurally identical to canaries. The only thing is now they carry the red gene. Canaries have also been crossed with European and American Goldfinches. Most of the time these offspring are sterile, but sometimes they're not.
 
Instead of Astragalinus and Pyrrhomitris the "Taxonomy in Flux" list based on the forthcoming Nguembock et al (2009) paper, uses Pseudomitris and Sporagra respectively.
A brief search through the Richmond Index on zoonomen.net would suggest that the first two mentioned would have priority.
Anyone care to comment? Laurent?

The type of Astragallinus is tristis, that of Pseudomitris is psaltria. As far as I can see, Astragallinus seems indeed to have unambiguous priority (1851 vs. 1865). But of course priority comes into play only if tristis is included in the genus... Ngembock et al. did not have tristis (nor lawrencei, btw) in their analyses - they only had psaltria, which appeared as a stand-alone branch.

I can't find Pyrrhomitris in the Richmond Index; Sporagra is dated as from 1 June 1850. Pyrrhomitris is dated by Ridgway as from 15 Sep 1850, and by Hellmayr as from "end of" 1850. Ngembock et al. may well be right on this one.

My main reason for posting though is because I wonder if this proposed generic split is really necessary. The 3 groups of Spinus form a fairly well-supported clade in for example:

Arnaiz-Villena (et al) (2007b), Bayesian phylogeny of Fringillinae birds: status of the singular African oriole finch Linurgus olivaceus and evolution and heterogeneity of the genus Carpodacus, Acta Zool. Sinica 53, 826-834.
Arnaiz-Villena (et al) (2008), Mitochondrial DNA Phylogenetic Definition of a Group of ‘Arid-Zone’ Carduelini Finches, Open Ornith. J. 1, 1-7.

Bayesian posterior probability was acceptable, but if you check other analyses in these and other publications by Arnaiz-Villena and colleagues, support is usually not good.
In Ngembock et al., it's mainly the nuclear gene (beta-fibrinogen intron 2) that appeared to have a signal disagreeing with this clade. It indeed placed spinus close to Loxia.
 
In Nguembock B, Fjeldså J, Couloux A, Pasquet E
Molecular phylogeny of Carduelinae (Aves, Passeriformes, Fringillidae) proves polyphyletic origin of the genera Serinus and Carduelis and suggests redefined generic limits.Mol Phylogenet Evol 2008 Nov 6. the abstract states “Within Serinus and Carduelis, the obtained phylogenetic structure corresponds well with the subdivisions suggested by H.E. Wolters, based on traditional methods. Thus, we support his generic subdivision (Ochrospiza, Dendrospiza and Crithagra for Serinus, and Chloris, Spinus, Sporagra, Pseudomitris, Acanthis and Linaria for Carduelis)”.

In 1865 Cassin set up six subgenera of siskin/goldfinch including Pyrrhomitris, Sporaga, Pseudomitris, and Astragalinus.
http://books.google.com/books?id=3n...&hl=en&sa=X&oi=book_result&resnum=1&ct=result . Does it matter that Pseudomitris was never set up as a genus? ICZN code Art. 11.9.3.5 says: A species-group name first published as an interpolated name cannot be made available by this act. Was it interpolated? But see Art. 4.2 and 6.1??

Stejneger in the Auk, 1884 set out the history of the names for siskin.
1760 Carduelis Brisson
1803 Acanthis Bechstein
1816 Spinus Koch
1826 Spinus Boie
1828 Chrysomitrus Boie
1851 Astragalinus Cabanis

The British said thanks but no. “Dr. Stejneger has with his usual care worked out the question of the priority of the generic name to be used for the Siskins and has adopted Spinus of Koch, for he allows Boie to have fixed the type in 1826. As, however Boie himself proposed the genus Chrysomitris for these birds in 1828 and the name has been in common use, I have not adopted this change which would alter a number of well known names without any adequate object. I agree in this particular case with the argument of Messrs. Salvin and Godman in favour of retention of Chrysomitris (Biol. Centr.-Amer., Aves i., p. 427)”
Catalogue of the Birds in British Museum, v. XII Fringillidae R. Bowdler Sharpe.

Pyrrhomitris’s type was cucullata, Red Siskin and Sporaga’s was magellanica, Hooded Siskin both South American birds.

Linaria is Bechst. 1802, but Chloris is a Möhring, 1752 name and I thought that names older than the 12th edition of (1758) cannot enter zoological nomenclature. Code Art. 3.
 
http://books.google.com/books?id=3n...&hl=en&sa=X&oi=book_result&resnum=1&ct=result . Does it matter that Pseudomitris was never set up as a genus? ICZN code Art. 11.9.3.5 says: A species-group name first published as an interpolated name cannot be made available by this act. Was it interpolated? But see Art. 4.2 and 6.1??

Can't see this on Google Books from here...
But it should not matter, because Pseudomitris is a genus-group name, not a species-group name. What applies here is:
"43.1. Statement of the Principle of Coordination applied to genus-group names. A name established for a taxon at either rank in the genus group is deemed to have been simultaneously established by the same author for a nominal taxon at the other rank in the group; both nominal taxa have the same type species, whether it was fixed originally or subsequently."​
If a name is offered as a subgenus, it is deemed to have been offered as a genus as well at the same time.

Linaria is Bechst. 1802, but Chloris is a Möhring, 1752 name and I thought that names older than the 12th edition of (1758) cannot enter zoological nomenclature. Code Art. 3.

The start of zoological nomenclature is defined as 1 Jan 1758, which is deemed to be the date of publication of the 10th (not 12th) ed. of Linnaeus' Systema naturae. (One work predating this is however included in the Linnean works as well: Clerck's Svenska Spindlar, that appeared in 1757 but is explicitly deemed by the Code to have appeared on 1 Jan 1758 too [and is therefore to be cited as "Clerck, 1758", which some arachnologists find quite insupportable... ;)]. The names in Svenska Spindlar have priority over those in Systema naturae.) Of course, this is all entirely arbitrary - the only thing that was needed was a clearly defined starting point.
As Möhring, 1752, predates the official start of zoological nomenclature, the names that it contains are not available from this publication. But this does not mean that they cannot enter zoological nomenclature at all. To enter it, they need to have been made available in a subsequent work (by an author who may simply have used them and pointed to the pre-Linnean work offering the necessary descriptions).
You may find Chloris attributed to "Möhring, 1758" in some places, but this was actually a simple Dutch edition of the 1752 work, and for this reason is not regarded as a real "post-1758" work.
Chloris is available from Cuvier, 1800.
 
But in the attached tree, for instance, the South-American birds look closer to spinus & pinus than to tristis, psaltria & lawrencei.

Interesting tree!

But look at the positions of Acanthis flammea v A. hornemanni :eek!:

Presumably the samples from New Zealand are from A. cabaret.

Genetically speaking is there really any more than one species of Redpoll?
 
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Genetically speaking is there really any more than one species of Redpoll?

No if you follow Marthinsen & al. 2008

Marthinsen, G., Wennerberg, L. & Lifjeld, J. T. 2008
Low support for separate species within the redpoll complex (Carduelis flammea–hornemanni–cabaret) from analyses of mtDNA and microsatellite markers
Molecular Phylogenetics and Evolution 47: 1005–1017
 
Arnaiz-Villena et al 2012

Arnaiz-Villena, A. et al. PHYLOGENETIC DESCRIPTION OF THE THREE NORTH AMERICAN CARDUELIS RADIATIONS. 2011 AOU Meeting in Jacksonville, Florida.
abstract
Arnaiz-Villena, Areces, Rey, Enríquez-de-Salamanca, Alonso-Rubio & Ruiz-del-Valle 2012. Three different North American siskin/goldfinch evolutionary radiations (genus Carduelis): pine siskin green morphs and European siskins in America. Open Ornithol J 5: 73–81. [pdf]

Also...
Arnaiz-Villena, Ruiz-del-Valle, Reguera, Gomez-Prieto & Serrano-Vela 2008. What might have been the ancestor of New World siskins? Open Ornithol J 1: 46–47. [pdf]

Peer-reviewed!!?? As with various earlier papers, sadly this journal doesn't help the case for open access publishing!
 
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Pine & Black-capped Siskins

Vallely, Dyer & Perktaş 2014. Perplexing siskins: a review of the Spinus pinus–S. atriceps problem. Bull BOC 134(4): 259–269.
SUMMARY.—Black-capped Siskin Spinus atriceps and the southernmost form of Pine Siskin S. pinus perplexus have long been confused. We outline the taxonomic history of the complex and present a review of morphological characters based on the largest series yet assembled. Olive-morph birds are morphologically distinctive and are correctly associated with the name atriceps, although Salvin's original description also included a grey-morph specimen.
Conclusions
Species limits in the S. atriceps / S. pinus complex remain poorly understood, and many authorities have followed van Rossem (1938) in suggesting that these forms hybridise and may be conspecific (e.g. Howell et al. 1968, AOU 1983, Sibley & Monroe 1990, Howell & Webb 1995, Clement 1993, 2010). The collection of additional vouchered, genetic material from the Chiapas and Guatemalan highlands is required to shed further light on the nature of plumage variation, species limits and perhaps phylogenetic relationships in the S. pinus / S. atriceps complex. Sound-recordings of vouchered specimens might also provide valuable data. Sampling, assembly and analysis of genetic data, together with data from the syntypes of S. atriceps and holotype of S. pinus perplexus, offer the best promise of lasting resolution.
Clement 2010 (HBW 15):
 
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South American siskins

Beckman E.J., Benham P.M., Cheviron Z.A. & Witt C.C., in press. Detecting introgression despite phylogenetic uncertainty: the case of the South American siskins. Mol. Ecol.

PDF
 
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