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Should we consider lumping more subspecies? (1 Viewer)

Maffong

Well-known member
Reading up on subspecies, I sometimes come upon statements that read something like: "Not readily diagnosable" sometimes not even with measurements. For example I tried to learn about Taiga Bean Goose subpopulations, but apparently it's impossible to distinguish Anser fabalis fabalis from A. f. johanseni.
Similarly, Bearded Reedling has three subspecies that differ slightly in plumage colour saturation, but other than that they’re identical. Perhaps some wing or beak measurements may differ slightly, but looking at migrationatlas.org there's so much movement between populations that I have a hard time believing that there’s a significant difference between Panurus biarmicus biarmicus and P. b. russicus.

Therefore, I would like to ask the birdforum crowd:
What's the use of subspecies that are not diagnosable (except perhaps by range) or only by minute characteristics? Do we need fewer subspecies?
And how should we treat subspecies that are morphologically identical to conspecifics but differ drastically in life history, such as vulpinus- and buteo-Common Buzzards or fuscus- and intermedius-Lesser Black-backed Gulls?
 
There is an "Ornithology Monograph" (publication series from AOU, the predecessor of AOS) in 2010 on the topic of subspecies validity. I could find the chapters using this search in SORA:

You will see all sorts of arguments for or against subspecies as concept, and also some agreement that some subspecies should be synonymized with others.
Niels
 
I think the importance is less in how identifiable they are in the field, and more that we have subspecies as a tool to differentiate between important populations in some way that recognizes their distinctiveness in a broader population sense and helps with conservation efforts.

The more we smoosh things up the easier it is to say 'we can lose that habitat and the species that use it because there are more of the same in that habitat over there.'
This is of course what happens anyway but the harder we make it the better IMHO.
 
Subspecies traditionally have had very little rigor applied to assessing and identifying them, often being named using very small sample sizes and subjective assessments of morphological variation. I think subspecies are useful, but a lot of the recognized ones probably are not.
 
Traditionally subspecies were just regional variants with minimal morphological differences, often described on the basis of few specimens. When there is a clear difference they tend to be promoted to species. The total number of bird species + subspecies hasn't changed significantly over time while the number of species had increased substantially (there's a table somewhere, possibly in the IOC update thread).

P.S. I think the traditional leopard and tiger subspecies were mostly described on the basis of surprisingly few skins (just one in several cases).
 
The definition/opinions of what a "valid" subspecies is has changed quite a bit since the 1700s so it may depend on what is meant and how many people will adopt it.

I've been surprised to see some mammal publications which refuse to recognize anything with clinal variation as a subspecies (essentially subspecies are defined as PSC species in their view). This is the opposite (I think) of the classic early Ernst Myer definition which used clinal variation as the defining reason that organisms would be subspecies instead of outright species - they have "intergrades."

In American herpetology, the philosophical pendulum has been in the opposite corner recently- I have been told that "the BSC doesn't make sense in herpetology" due to limited mobility of those animals, and that integration/hybridization is no barrier to a species concept. In that scheme, subspecies designations are similarly discouraged in favor of what I guess I would call "morphotype species" with extended hybrid zones. Check out the recent Peterson Guides to reptiles and amphibians for some interesting examples and range maps.

Personally, I think its worthwhile to have a name for anything that is different, if possible. In other words, if a morphotype (geographically correlated or otherwise) is not called a subspecies, then what do we call it? Do we really want publications burdened with having to refer to "the big darker plumaged Song Sparrows from coastal Alaska" when we could have an easy shorthand? I agree that the diagnosis of some subspecies can be kind of a stretch, so to speak - when they are defined only by something like bill length, or a slighter shade of brown. But if these are real differences, I see no problem with naming them. And if those differences have a geographic correlation - those are subspecies... at least according to some of us.
 
I'm not arguing against subspecies as a whole concept. For example the Yellow Wagtails taxa are clearly very different even when they hybridise in small contact zones.

But subspecies of birds like Willow Tit, Bearded Reedling or the Bean Geese (both Tundra and Taiga) don't make much sense to me, as there's no way to verify our current classification as differing subspecies, because the ID criteria are too weakly differentiated and the distribution is likely clinal.
 
What's the use of subspecies that are not diagnosable (except perhaps by range) or only by minute characteristics? Do we need fewer subspecies?
And how should we treat subspecies that are morphologically identical to conspecifics but differ drastically in life history, such as vulpinus- and buteo-Common Buzzards or fuscus- and intermedius-Lesser Black-backed Gulls?
I like Kirk Roth's answer to your broader question above, but as concerns vulpinus vs buteo Common Buzzard or fuscus vs intermedius LBBG, I would not consider them morphologically identical, in fact they are quite distinct for the most part. Not all individuals can be safely identified, especially out of range, but this does not mean that they aren't different taxa (and I think fuscus LBBG was treated as a full species for some time by the Dutch, right?)
 
The definition/opinions of what a "valid" subspecies is has changed quite a bit since the 1700s so it may depend on what is meant and how many people will adopt it.

I've been surprised to see some mammal publications which refuse to recognize anything with clinal variation as a subspecies (essentially subspecies are defined as PSC species in their view). This is the opposite (I think) of the classic early Ernst Myer definition which used clinal variation as the defining reason that organisms would be subspecies instead of outright species - they have "intergrades."

In American herpetology, the philosophical pendulum has been in the opposite corner recently- I have been told that "the BSC doesn't make sense in herpetology" due to limited mobility of those animals, and that integration/hybridization is no barrier to a species concept. In that scheme, subspecies designations are similarly discouraged in favor of what I guess I would call "morphotype species" with extended hybrid zones. Check out the recent Peterson Guides to reptiles and amphibians for some interesting examples and range maps.

Personally, I think its worthwhile to have a name for anything that is different, if possible. In other words, if a morphotype (geographically correlated or otherwise) is not called a subspecies, then what do we call it? Do we really want publications burdened with having to refer to "the big darker plumaged Song Sparrows from coastal Alaska" when we could have an easy shorthand? I agree that the diagnosis of some subspecies can be kind of a stretch, so to speak - when they are defined only by something like bill length, or a slighter shade of brown. But if these are real differences, I see no problem with naming them. And if those differences have a geographic correlation - those are subspecies... at least according to some of us.
Birds are almost the perfect organisms for BSC...which is very hard to test in most other groups. You can readily notice differences in display, display structures, and calls which are virtually impossible to notice with the naked eye in most herps and mammals. Also birds are generally a lot easy to just observe in the wild. I mean there is a reason why birding is more popular than mammalwatching!

I personally tend to like Remsen's view of treating phylogenetic species as subspecies and biological species as species. It provides a less vague for what a subspecies actually represents and integrates two different popular species concepts into bird taxonomy.
 
Reading through the early editions of British Birds much of the drive to identify new sub-species seem to be nationalistic. There seemed to be a craze to have a British sub-species of every bird they could. Few to none of these sub-species seem to have survived modern rigour.
 
a good number of subspecies probably would not withstand rigorous re-analysis (even recognizing that plenty already have been synonymized). it's a lot of work to assembly all relevant specimens and document that differences between a particular set of subspecies are trivial or non-existent, however, and I suspect that there's also not a great deal of glory in publishing that kind of a paper. that's my take on how we remain stuck with so many zombie subspecies.
 
Shirihai & Svensson's intro on subspecies in the HWPB is worth reading. They went for a quantitative (morphological) diagnosability criterium, resulting in "about 15% fewer subspecies compared to other handbooks". And they do recognize Panurus biarmicus russicus.
But the 75% rule means that quite a few individuals might not be identifiable to subspecies on plumage characteristics, in the field or in the hand.

We have made an effort to independently assess all described subspecies that appear in modern ornithological literature within the range covered by the book. This has forced us to spend much time in museum collections, the only place where series of closely related but differently named subspecies can be compared side by side.Between the two of us we have spent many, many months in museums in order to write this handbook. One important object of this laborious work has been to decide whether a subspecies is sufficiently distinct to be recognised and treated as separate from other subspecies of the same species. We have, by and large, tried to apply the so-called 75% rule (e.g. Amadon 1949), meaning that at least three-quarters of a sample of individuals selected at random (in some cases of one sex or age) ofa subspecies must differ diagnosably from other described subspecies within the examined species. The specimens selected for assessment should as far as possible be from similar age categories and seasons to allow for the most comparable plumages to be fairly assessed. The main limiting factor for this part of our work hasbeen the scarcity of comparable material of some taxa in collections.
We have long felt the need to focus on distinct subspecies and to dismiss the many subtle or even questionable subspecies that were perhaps based on too short series or on skewed or inadequate material, or which in reality represented only minor tendencies within a population, far from the minimum 75%. Natural variation within any one population has often been underestimated when new subspecies have been described. In our opinion, it is better to concentrate on clear differences, and to account for slight clinal tendencies or deviations from the most typical under a single subspecies heading, rather than to create a confusing mosaic of subtle or dubious but formally named subspecies. Most of the final assessment of subspecies taxonomy was done by LS.
Compared to other handbooks and checklists, we accept about 15% fewer subspecies. Those deemed to be too similar to a neighbouring race to be upheld have been lumped with that race and treated as a synonym.
Much geographical variation within continentally distributed species is smooth and gradual, this variation usually being termed clinal. There are taxonomists who tend to see this as a problem and who prefer to treat the entire such range as one subspecies. It is true that clines create circumscription difficulties. However, we prefer to judge every case by its own merits; if the ends of a cline are very different,a minimum of two named subspecies seems reasonable, one at each end and with a diffuse centre of intergrading characters. If there are hints of stepwise change along the cline, these suggest subspecific borders and lead to recognising additional subspecies along the cline.
We want to stress that the definition of a subspecies is based on morphology.If size, structure, colours or patterns differ with sufficient consistency (in this work,as stated, by at least 75% of the examined specimens of at least one sex or age)within a geographically defined part of the range of a species, then it is a valid and distinct subspecies irrespective of whether an examination of its mitochondrial DNA or another genetic marker reveals no clear genetic difference from neighbouring subspecies. Geneticists are sometimes so impressed by their new tool that they forget these prerequisites and distinctions. If we are to re-define subspecies by their genetic properties, all existing subspecies need to be discarded and all work on geographical variation redone in laboratories. But in such a case, scientists need first to agree on exactly which genetic definition all variation is to be judged against. Since this is unlikely ever to happen, we had better stick to the morphology-based subspecies taxonomy we already have!
It is best to add that our approach to subspecies taxonomy is quantitative rather than qualitative. If a described taxon does not in our view reach the required level of distinctness, we place it in synonymy under a senior name. But that does not mean that we claim to know better than others regarding the recognition of a valid taxon,only that it is not in our view distinct enough according to our requirements. If others prefer to describe every tiny variation under a formal name it is up to them.
Subspecies deemed by us to be borderline cases as to whether they are warranted or not, and subspecies only differing very subtly from other valid subspecies, have been marked with an open circle in front of their names. For subspecies that are either for some reason questionable, or for which we failed to find sufficient or indeed any material, a question mark has been placed in front of their names. Subspecies known or suspected to be now extinct carry a dagger mark in front of the name.
At the end of each subspecies entry a selection of synonyms has been listed alphabetically within brackets; these are subspecies names that appear in the literature or on some specimen labels in museums but which are either junior synonyms or are invalid for one reason or another. They are shown as a service to the reader and to make it clear that they have not simply been overlooked by us. We have as a rule only included the more recent and commonly seen synonyms, but a few older or more rarely used ones have also been included if considered helpful to the reader. Anyone seeking a more complete list is referred to Sharpe (1874–99), Hartert(1903–38), Peters et al. (1931–87) or Vaurie (1959, 1965).
 
Shirihai & Svensson's intro on subspecies in the HWPB is worth reading. They went for a quantitative (morphological) diagnosability criterium, resulting in "about 15% fewer subspecies compared to other handbooks". And they do recognize Panurus biarmicus russicus.
But the 75% rule means that quite a few individuals might not be identifiable to subspecies on plumage characteristics, in the field or in the hand.
Yet, they didn't manage to produce a single picture of russicus or kosswigi in their book...
 
Interesting is that the number of new subspecies split in the last 20. years was comparatively small compared to the number of the new species split. Because a new subspecies does not give the same publication popularity.
 
Yet, they didn't manage to produce a single picture of russicus or kosswigi in their book...
Panurus biarmicus russicus BREHM 1831 (here), as "Mystacinus Russicus", and Panurus biarmicus kosswigi KUMMERLOEVE 1959 (here).

Looks like the Author of the latter subspecies, already in 1961, had some doubts himself (here, even if he also/still listed kosswigi on page 282). Also see Spitzer (1973) here. Or van den Elzen (2010) here (alt. here).

Some actual specimens of "russicus"; here, here, and here

If different enough? I haven't got a clue ...

To tell them apart, you need to be a far (far) better birdwatcher than I am ... :rolleyes:

Either way, hopefully the above was of some help/use?
 
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I must admit I get confused by all of this - when I suggested American Coot and Eurasian Coot might one day [potentially get lumped, it was pointed out that they have different facial features and bills, but isn't that the same for Crossbills?
 
Personally I'm very fond of the Darwinistic "if two individs can breed and produce fertile offspring (both male and female must be fertile, mind you!) they belong to the same species".
Subspecies is elsewhere in zoology (which includes ornithology as a subspecies!) used to define genetically consistent variants within a species. All the dabbling with minute DNA variations to differentiate species is treading on thin ice: you need large numbers of genotypes within one species in order to predict what is to be expected within the species, and even more to be able, based on genotype, to call it a different species.
Geographically separate populations may after time form subspecies which in turn may differentiate into a new species given even more time and isolation and inbreeding.
 
I personally consider subspecies as a sort of a Wild West rank, which contains both very well defined subspecies, like Red-spotted and White-spotted Bluethroats and subspecies which are only recognizable on average on a series of specimens (like many endemic British songbird subspecies). But I may be influenced by mammals. Subspecies of many mammals, some well known ones, were never properly revisited.
 

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