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Used to be the norm. Check books etc up to the 60s/70s/80s. You like many do not know your not so distant paleohistory LoL.
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Thomas R. Holtz, Jr.
Email: tho...@umd.edu Phone: 301-405-4084
Principal Lecturer, Vertebrate Paleontology
Office: CHEM 1225B, 8051 Regents Dr., College Park MD 20742
Dept. of Geological, Environmental, and Planetary Sciences, University of Maryland
http://www.geol.umd.edu/~tholtz/
Phone: 301-405-6965
Fax: 301-314-9661
Faculty Director, Science & Global Change Program, College Park Scholars
Office: Centreville 1216, 4243 Valley Dr., College Park MD 20742
http://www.geol.umd.edu/sgc
Fax: 301-314-9843
Mailing Address:
Thomas R. Holtz, Jr.
Department of Geological,
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> This also feels like a uniquely made-up bird paleontology problem. Please correct me if I’m unaware, but nobody seems to be fighting desperately to preserve a definition of Mammalia that keeps things like tritylodontids in the crown, despite ~120 years of similar literature baggage.
This absolutely does happen in mammalian paleontology, you just don’t hear about it because mammalian and dinosaur paleontologists tend to run in separate circles. This is actually much more a problem for mammal (and fish) paleontology because we have many more extant groups to worry about rather than just considering how things are positioned relative to modern birds and crocodiles.
To use one example, the group I work on — the Sparassodonta — used to be classified as marsupials. The group containing sparassodonts and their allies (Pucadelphyida) appears to be part of a broader radiation that occurred when metatherians dispersed to South America right around the K-Pg boundary, and represent an evolutionary relevant grouping that contains virtually all Cenozoic metatherians (whereas the Mesozoic forms and the handful of Cenozoic stragglers in the Northern Hemisphere are basal). By this point in time the marsupial body plan was well-established and sparassodonts would be biologically indistinguishable from any crown marsupial in terms of general appearance or physiology.
However, because sparassodonts happened to branch off just barely before opossums did and had the bad luck to die out maybe 1 to 2 million years before the present day, they are classified as stem metatherians and “marsupial” does not refer to that nice neat group that includes the South American/Australian Cenozoic metatherian radiation. This makes it very awkward to talk about sparassodonts, especially with laypeople, and often causes people to ask very silly questions like “Did sparassodonts lay eggs? I know they’re not considered to be marsupials anymore so does that mean they laid eggs?” Believe it or not, that’s not even an isolated example but something I’ve seen repeatedly be asked.
The same issue occurs with Mammalia as a whole. Evidence is increasingly suggesting that the typical mammalian body plan (e.g., extensive hair, milk production, diphyodonty) was mostly assembled in a rapid burst of morphological evolution that happened around 220 million years ago. There is a fairly stark morphological divide between “traditional” mammals like Morganucodon and more stemward cynodonts like tritylodonts. Originally everyone was pretty fine with drawing the line for mammals around Morganucodon, but with the advent of crown clades now some people advocate for restricting the definition to the most recent common ancestor of monotremes and therians and calling everything else a mammaliaform or something.
This actually causes more problems down the line because while we know how monotremes and therians are related to one another due to genetics, we actually don’t have a good idea of how these various extinct groups fit into this broader picture and thus who is in the crowd and who is in the stem. We can vaguely point to several groups like eutriconodonts and dryolestoids that seem to be more on the therian line of things, and we have some things that seem to be stem-monotremes (ausktribosphenidans), but with things like haramyidans, euharamiyidans, multituberculates, docodonts, and gondwanatheres it’s anyone’s guess where they go. Adding to this the actual split between crown and stem mammals is based solely on genetic evidence. Genetic data suggests it probably happened somewhere in the middle Jurassic but there’s almost no data to suggest what that ancestor would’ve looked like and if you had a time machine I would bet that you probably couldn’t reliably tell whether a very basal crown mammal was on the crown or the stem; The definition is purely semantic rather than biological. On top of that, there aren’t really any true synapomorphies that diagnose crown mammals relative to other mammaliaforms, many of the features that are shared between monotremes and therians like fully detached inner ear bones appear to have evolved independently between the two groups.
So yeah, a lot of mammal paleontologists hate it and much like Archaeopteryx most of us just conveniently ignore that "mammal" is supposed to only refer to the last common ancestor of platypodes and people and go with the traditional definition simply because it makes it easier to explain to people what exactly we are looking at and why it matters in terms of the broad scheme of things.
There’s actually other cases that are even worse than this. I always like to point out the example of Meiolaniiformes as an example of just how badly restricting crown group definitions to extant taxa can get. Meiolaniiformes are a group of turtles that, as far as we can tell, seem to be really, really basally positioned within the clade. They also survived really, really recently, I think there are carbon-dated meolaniid remains from New Caledonia that date to the third century A.D. and they survived long enough for humans to encounter them (and wipe them out). But, because they are no longer living there are considered stem turtles rather than crown turtles.
Or, consider that the most recent data on dasyuromorphian marsupials recover thylacines is outside the clade of numbats + dasyurids. Do we consider thylacines “stem dasyuromorphians”? They became extinct before the advent of cladistic methodology but they were known to Western science for about 120 years before they actually went extinct.
I pointed this discrepancy out to someone once and their argument was “we should only consider something belonging to the stem or crown group if it was alive at the time it was discovered by Western science”. Which seems like a really myopic and problematic way to go about doing things.
100% agree. The point of taxonomic nomenclature is twofold: to describe the underlying architecture of the tree of life and to give us the tools to communicate with one another about patterns observed in nature. This “architecture” does not just mean branching order but also biological and ecological information. In many cases we want terms to be able to describe organisms with similar features, even if they aren’t explicitly monophyletic. For example, most ornithischian paleontologists recognize the utility in contrasting “iguanodontians” with hadrosaurs, even though everyone is aware “iguanodontians” are a non-monophyletic group. Or consider Stuart Sumida’s recent review of “pelycosaur-grade synapsids”. While it’s clear pelycosaurs are not monophyletic they are still so similar to one another in terms of morphology and likely paleobiology than either therapsids or non-synapsid reptiliomorphs it’s most effective to talk about them as a (non-monophyletic) group. As long as people are aware of what’s being talked about and it’s clear that referring to a group colloquially does not equal relatedness that’s fine.
Or how about “non-avian dinosaurs”. Everyone understands birds are nested deep, deep within dinosaurs but no one has a problem thinking that a hadrosaur and a tyrannosaur are going to be more similar to one another than a pigeon in many aspects of their biology, evolutionary history, ecology, taphonomy, etc., due to factors like birds generally being smaller than all other non-avian dinosaurs, volancy, and the fact that non-avian dinosaurs were wiped out in the K-Pg extinction. There are going to be some awkward gray areas like Archaeopteryx and other non-avian deinonychosaurians, but you can mostly put things into the two boxes. If there wasn’t value in distinguishing between the two groups no one would use the term “non-avian dinosaur” at all, even though at this point virtually everyone agrees that birds are just a form of dinosaur.
This is something that Linnaeus had in mind when he proposed his classification because he explicitly grouped together things that we know today are not closely related but filled roughly similar ecological roles and had loosely similar morphology (e.g., classifying sloths with primates, viverrids with mustelids in the first Systema Naturae. This isn’t to argue we should be grouping species non-cladistically but to highlight biological similarity is an important component in how terminology is used. Arguing that Linnaeus would not have classified Archaeopteryx as a bird is kind of a non sequitur because Linnaeus died 100 years before the first specimen of Archaeopteryx was actually discovered and one could very well argue he would’ve classified it as a bird because that’s how most scientists treated it back in the days of Linnaean taxonomy.
The problem is the way distinctions between crown groups and stem groups are made nowadays it doesn’t actually help science communication and in my experience watching how the general public have used (and abused) this idea is primarily utilized by the “uhm acktually” types who want to sound smarter than everyone else by pulling out some technicality that doesn’t actually help the ideas that are trying to be communicated. If you’ve ever seen that Futurama joke about “actually, the [spider aliens] are actually more closely related to our elephants than are spiders”, you know exactly what I’m talking about. The difference isn’t relevant 99% of the time, and I’ve frequently seen it confuse people who don’t really understand the difference between stem and crown groups. A good example of this is the one I gave above about “did sparassodonts lay eggs?” Sharks are a particularly bad case of this, where a lot of paleo-shark fans like to argue online and in-person that ctenacanths, cladoselachians, xenacanths, and hybodonts aren’t sharks because one researcher in the field really promoted that idea in sci comm, but in reality most shark paleontologists call all these forms “sharks” because they are ecologically and functionally similar and only distinguish between crown sharks (neoselachians) and more basal forms where necessary. For the most part they don’t seem to have a problem with treating chimaeras and rays as weird, mutant sharks the same way dinosaur paleontologists treat birds as just another branch of dinosaurs.
One could argue that the failure of the general public to think in terms of cladistic methodology, but the problem is human beings generally don’t think this way. When you tell someone “Archaeopteryx isn’t a bird, it’s a non-avian avialaean”, they don’t interpret it as “it’s not a bird but it’s slightly more basal on the family tree and doesn’t have all the features of modern birds” they interpret it as “it’s not a bird, it’s some other thing”. And unfortunately even trying to teach them a cladistic mindset is difficult long term because unless there a student in a field that regularly uses phylogenetics (which doesn’t even include all of biology, to be frank, I know a lot of doctors and most don’t even understand that E. coli is supposed to be a scientific name), they are going to forget about it as soon as they leave the classroom because such a mindset doesn’t have many applications in their daily life. It just doesn’t work in terms of science communication, especially in terms of trying to get across to the lay public exactly what something is.
And that’s not getting into the really weird cases where I’ve seen people argue things like “Mesohippus or even Equus simplicidens aren’t horses, they’re stem equids because they're outside the MRCA of modern Equus”, which just completely confuse people who are trying to wrap their heads around horse evolution. Like yes, they're not in the crown, but calling them "not horses" just makes things kind of ridiculous. Equus simplicidens is a one-toed, hypsodont horse that just happens to be from the Pliocene, why call it something majorly different?
It’s really frustrating because despite this long rant I actually prefer the simplicity and elegance of cladistic methodology, and I'm not trying to argue for freaking phenetics, but the way cladistic terminology gets misused so often makes things worse rather than better. The entire point of cladistics was to put some rigor into taxonomy rather than get in pointlessly semantic slap fights over whether some group should be at a family (-idae) or superfamily (-oidea) rank, but in many cases all it's doing is creating new semantic arguments. It gets really difficult because many biologically meaningful, monophyletic groups that your average person would recognize as "a thing" do not easily map onto the crown versus stem dichotomy because of extinctions, which is an accident of history more than reflecting actual patterns of relatedness and divergence (and in the case of "we should only consider something extant if it was alive when [mostly] European scientists discovered it" opens up a can of worms). Similarly, I understand the I should just do what I value in recognizing the difference between stem groups and crown groups, especially when talking about genetic data or soft tissue features that can’t easily be established in fossils, but the way these concepts are used in many cases only makes science communication worse, rather than more effective.
> BTW I have a way to explain birds being dinosaurs to people. They often ask what that means. I say are bats flying mammals? They say yes. I then say birds are flying dinosaurs. I always see the aha realization of the explanation in their eyes.
That's the way I always try to frame it, as well/
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