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Archive for February, 2015

Coddling Caudals

Think of a region of general mammalian anatomy. You’re probably not thinking of the tail. We’re mammals and yet have reduced ours to a puny coccyx embedded in muscle and fat. It’s an alien organ to us. Let’s face it, the tail gets the short shrift when it comes to morphological, functional and evolutionary studies in tetrapod vertebrates. There are notable exceptions such as in studies of prehensile tails or the role of the tail in cetacean locomotion, but broadly we know far less about the caudal vertebrae of mammals than we do about heads or limbs or some other bits. It is timely to coddle caudals: to talk about tails, not turn tail and run rostrally. This post wags its tail affectionately at the topic.

No blog post on tails is complete without a photo of the business end of Euoplocephalus's (Ankylosauria) caudals.

No blog post on tails is complete without a photo of the business end of Euoplocephalus’s (Ankylosauria) caudals.

Thagomizer.

Thagomizer of Stegosaurus. But of course!

Stomach-Churning Rating: well, there are some rancid emu butts, so I’m giving a 7/10; but otherwise mostly just line drawings.

My team has done a bit of work trying to better appreciate the tail as part of our expanded emphasis on the evolutionary morphology and biomechanics of the vertebral column; not just limbs as I was used to. Former PhD student Michael Pittman did his whole thesis on the evolution of tail form and function in dinosaurs, publishing a nice PLOS paper on theropod tail evolution, with other cool stuff in the pipeline. Pittman visited our lab recently with collaborator Heinrich Mallison to gather new data on the tails of archosaurs, focusing on Nile crocodiles and emus as an initial phylogenetic bracket. In my team’s prior work, we’d dabbled with theropod tails, focusing on the caudofemoralis muscle of theropod dinosaurs like T. rex, and on the size of the tail and its effects on the body’s centre of mass, following up on super-duper classic work by my mentor Steve Gatesy. So we have some caudal street cred, but we don’t have the tiger by the tail. (Hang in there, I’m going to milk the tail puns here!)

Don’t be afraid to touch the tail pics- they lead to bigger versions.

Mallison and Pittman know how to coddle caudals!

Mallison and Pittman know how to coddle caudals!

"Emu butt"- the tail is hidden in the smelly bulb of fat on the left side.

“Emu butt”- the tail is hidden in the smelly bulb of fat on the left side.

Bending an emu tail to measure its stiffness.

Bending an emu tail to measure its mobility.

Emu tail bones: our collection

Emu tail bones: our collection

I was inspired to write this post because of Michael’s visit, which gave me the opportunity to shoot some deliriously disgusting images of “emu butts” during the dissections and CT scans, but also got me thinking more about tails. And as usual, I poked around the literature looking for tall tales of tails.

I ran across one of those great review papers that is fodder for a hundred or more research projects: “The mammalian tail: a review of functions” (1979) by Graham C. Hickman (Mammal Review 9(4): 143-157. The rest of this post reviews his review.

Hickman, like I do here, starts off by reminding us of the tail’s neglect in science; e.g. “modifications of caudal vertebrae such as lengthened zygapophyses and neural spines are not as striking as the flexibility shown in the changing length and fusing of limb bones.” True that, but Hickman adds the great turn of phrase “A rodent chewing off its leg to escape a trap seems much more of an extreme than chewing off the tail, though it has four legs and but one tail.” Then he runs through a general overview of the diversity of tail forms and functions in mammals, with plenty of citations of older literature (there’s bound to be much to find in the tailings from the goldmine of 1800s German morphology papers, too).

What would a giant anteater look like without its tail? Odd indeed.

HickmanFig7

Mammalian tails range from four caudals in us freakish humans (does no mammal naturally have fewer, or have truly lost the tail? I wonder if anything has been missed) to fifty in pangolins (huzzah!). Breeds of dogs seem not to vary as much in terms of tail bone count as I’d expect: 20-23. But Hickman’s mention of Thorington’s (1970) study showing that mouse embryos raised at higher temperatures develop longer tails grabbed me… and reminded me of groundbreaking work that RVC PhD student Andrea Pollard is doing with temperature effects on bird and crocodile limbs (stay tuned).

Figure 2 in Hickman (1979) was what grabbed me most, depicting tail disparity in mammals. It’s a figure that gets your tail thumping. Check it out:

TO ADD

Anatomical disparity of mammalian tails! A, Black Rat; B, 9-banded Armadillo; C, Grey Squirrel; D, Horse; E, Fallow Deer; F, Wooly Spider Monkey; G, Coatimundi; H, Beaver; I, Bottle-nosed Whale; J, Manatee; K, Flying Squirrel; L, Fat-tailed Gerbil; M, Scaly-tailed Squirrel, N, Plains Pocket Gopher; O, Porcupine; P, Grey Kangaroo; Q, Naked Sand-rat; R, Big Brown Bat; S, Merriam’s Kangaroo Rat; T, anonymous Glyptodont; U, Ceylon Shrew.

Boom!

Hickman continues on to consider tail functions and behaviours, commenting that most bipedal mammals have long tails whereas humans buck the trend. Pangolins and anteaters get due mention here, but I really liked the factoid that “Beavers occasionally walk bipedally with an armload of mud” (p.145).

Mammals, like other vertebrates, that have substantial tails tend to use them for locomotor support at least when moving slowly, and Hickman lists kangaroos+kin, anteaters, pangolins and beavers as examples of mammals that thus use their tails as “fifth limbs”. But there are stranger tail functions in mammals than this ancestral tail-prop role. The bat Nycteris has a singular tail that ends in a “T”, bracing the uropatagium (tail-leg membrane).

Lovely kangaroo sculpt/skeleton from the incomparable comparative anatomy museum in Paris.

Lovely kangaroo sculpt/skeleton from the incomparable comparative anatomy museum in Paris.

However, some mammals also don’t use their tails the way we might expect- the platypus (Ornithorhynchus) doesn’t power its swimming with its tail so much as it uses it for stabilization, according to Hickman; paddling with the limbs seems more important (but this could use some modern scientific study using proper hydrodynamic testing). Yet they do use their tails to tamp the earth of their burrows and, curling them up to their belly, to bring in vegetation and such to provision their nests, as well as using their tails as energy stores (like many animals do). In contrast, beavers don’t transport much with their flat tails, whereas the more prehensile tails of pangolins may be used for carrying their babies.

HickmanFig5

Hickman notes how few mammals use their tails as weapons to harm others, although he properly brings up glyptodonts as a counter-example.  And then comes the striking description of how, by a “grinding motion of the tail against the body” a pangolin “almost severed the fore paw of a dog.” (p.148) And then, other mammals do the opposite of tail weaponry: Hickman cites that some 15 species of rodents can shed their tails (autotomy) as a defense, and like salamanders or lizards, regenerate them. Autophagy (self tail-cannibalism), however, Hickman rightly infers is a pathological, desperate condition, not a normal adaptation in mammals.

Big glyptodont tail club!

Big Glyptodon tail club!

More glyptodont tail clubs!

More glyptodont tail clubs! Neosclerocalyptus

Giant armadillo, showing glyptodont-lite version of the tail.

Giant armadillo Priodontes, showing glyptodont-lite version of the tail.

Need to motivate a rat to solve a maze puzzle or eat food? Pinching the tail had been shown to help, Hickman explains. This fits with the more obvious role of the tail in mammalian communication, including scent-marking. Here, Hickman notes that rather than using scent glands, hippos take the feces way out and just whip their tails around while pooping to spread their perfume. Which the internet knows well…

And then, finally, Hickman gets to the Rat Kings, which had me incredulous at first… but there are a bunch of references, so… What’s a Rat King? A “ball” of rats (from 3 to 32 of them!) with their tails tangled together for “group cohesion”, fabled in European stories for centuries but possibly “a frequent phenomenon” (p.152). An explanation for this phenomenon, Hickman explains, is confinement of rat in enclosed spaces where their tails do get entangled, only to be “found during a cold part of year, usually as a result of loud squealing noises which drew attention to the hide-away.”(p.153) In surveying the amusing range of explanations through history for Rat Kings (“itchy tails”?), Hickman relents and concludes “perhaps the tails of Rat Kings function best as cocktail discussion.” I concur—and append blogging discussion to that!

HickmanFig9

Tails you win, pre-caudals you lose, but Hickman’s review article is full of win! There’s plenty more of interest in there. I hope you enjoyed the look back at this classic paper, and at the tales that tails tell. This is the tale end.

I’ll let Ray get your caudals shakin’ as we depart:

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Owing Owen

It’s Darwin Day 2015 (or will be shortly), and also on this blog it’s Freezermas, a time of contemplative dissection of morphology and its history. This year I won’t be doing the crazy 7 posts in 7 days that I’ve done before (see 14 past ones here), and I won’t be doing a customary homage to Darwin. Instead, I’m dedicating today’s post to Richard Owen, oft characterized as Darwin’s greatest nemesis. Blasphemy? Nah. I’m a Darwin fan, sure, but today Owen gets his due from me. This post is like a “Top ten things you didn’t know about Richard Owen” post, but without the list, and some of them might be things you know, and I’m not even sure if there are ten of them, but they tend to be about Richard Owen. I feature a bunch of Owen’s papers’ coolest artwork, with links to the free versions of those papers, too. Bone up!

Stomach-Churning Rating: 3/10 for woodcuts that would otherwise be graphic. 7+/10 for rabid Darwin fans.

Owen was one of greatest (vertebrate) anatomists ever, if not the greatest (Alfred Romer gives him a run for his money in my opinion, but was less of a conceptual revolutionary). He was a key player in the divorce of the Natural History Museum from the British Museum and thus its move to its current South Kensington home in London as well as its autonomy and rise to scientific and cultural prominence. Hence, like today’s post’s title indicates, we owe Owen a lot as morphologists and as fans of biology (i.e. natural history). Indeed, his contributions are often undersold in deference to Darwin’s, and in service to a conventional narrative (written by the victorious Darwinians) in which he plays a villainous role. Even if one cannot admire the man as a touchy-feely kind of dude, his work demands respect and historiographic justice.

Rupke

I was inspired to write this post after reading a biography of Richard Owen some months ago: “Richard Owen: Biology Without Darwin, a revised edition”. It’s a fascinating read, and makes some points that challenged my naïve views of the history of biology, especially evolution and Victorian science. Author Nicolaas Rupke hammers home that pro-Darwin propaganda relegated Owen to a more minor and infamous position in the history of science than he deserved, defaming him as a cold-hearted, scheming, inconsistent jerk. This biography admits truth to Owen lacking some social graces and playing tough politics sometimes, but reminds us of his eminence in British science, which reverberated globally and was in no small part due to his determined drive and strategic rigour. I recommend the book to any fans of natural history and science, especially morphology. Indeed, Rupke’s 2009 edition was released in paperback for the Darwinian centennial, as an abridgement of his 1994 book. If you want to know more about Rupke’s 2009 book, there are informative reviews by Switek here and Lynch here. This biography humanizes Owen and casts away some of the demonizing. Scandalous snippets of Darwinians politicking against Owen are memorable– e.g. Owen’s “contest against the surrounding agencies” was a predecessor to Darwin’s “struggle for existence” and natural selection, which Darwin downplayed (Rupke, pp.157,169-171).

As Rupke’s work emphasizes, Owen was a pre-Darwininan evolutionary biologist, not a creationist. He devised an “axiom of the continuous operation of the ordained becoming of living things” that qualifies as evolutionist, but not transmutationist. He had ideas about evolution that just seem odd to a post-Darwinian mind, especially an “internalist” driving mechanism for evolution (something about the embryo that causes evolution to proceed; not a primarily external, environmental impetus as Darwin favoured), leading to orderly patterns of evolution, not the higgledy-piggledy bushy evolution of Darwin and his successors (e.g. Gould). To a modern evolutionary morphologist, Owen’s “transcendental morphology” echoes of earlier continental European work by Oken (& fellow Germanics), Cuvier (& fellow French) and others, and as such often feels strange – even mystically religious (pantheistic) or unscientific. And, like many Victorians, the idea of apes including, and a subset being ancestral to, humans repulsed Owen. That revulsion seems to have clouded his judgement on the scientific matters involved, which he famously sparred over with Thomas Huxley.

Forelimbs of Archaeopteryx compared with falcon, Pterodactylus, and humerus of a raven (left to right). From: Owen, R. (1863). On the Archéoptéryx of von Meyer, with a description of the fossil remains of a long-tailed species, from the lithographic stone of Solenhofen. Philosophical Transactions of the Royal Society of London, 33-47. http://www.jstor.org/stable/108788 FREE!

Forelimbs of Archaeopteryx compared with falcon, Pterodactylus, and humerus of a raven (left to right). Owen classifed the former as a bird, with potential relationships to pterosaurs (Rupke, pp.175-6); Darwinians like Huxley instead saw the dinosaurian, reptilian ancestry.
From:
Owen, R. (1863). On the Archéoptéryx of von Meyer, with a description of the fossil remains of a long-tailed species, from the lithographic stone of Solenhofen. Philosophical Transactions of the Royal Society of London, 33-47.
http://www.jstor.org/stable/108788
FREE!

However, we can credit Owen- like Lamarck and Geoffroy Saint-Hiliare in France- as an early “evo-devo” scientist trying to link transformation across lineages with developmental mechanisms. We can also celebrate Owen as one of the foremost early champions of the study of osteology as a worthy scientific pursuit in and of itself. Much of Rupke’s biography is structured to focus on the institutional structures that Owen played such a pivotal role in creating, especially the curated collections of the Natural History Museum (which Owen spent ~1856-1881 fighting to establish as its own facility!). Owen’s vast monographs on Cretaceous Reptilia, the flightless moa (e.g. Dinornis; with papers covering 40 years of research that continued almost up until Owen’s demise) and odd Gondwanan mammals of the Australian colonies (many of these specimens having been shipped to the museum by Darwin for Owen’s own studies) cement his status as an integrative collections-based researcher who did not eschew palaeontological research “because biologists don’t do that”, or some such divisive nonsense that we still encounter today.

Skull of a crocodile, exploded to show homologies of the bones; and a forelimb for added context. From: Richard Owen, Report on the archetype and homologies of the vertebrate skeleton. BAAS. https://archive.org/details/reportonarchetyp00owen FREE!

Skull of a crocodile, exploded to show homologies of the bones; and a forelimb for added context.
From:
Richard Owen, Report on the archetype and homologies of the vertebrate skeleton. BAAS.
https://archive.org/details/reportonarchetyp00owen
FREE!

Foetal skeleton of a human, with skull exploded for comparison of homologies. From Owen 1847 as above.

Foetal skeleton of a human, with skull exploded for comparison of homologies.
From Owen 1847 as above.

Speaking of palaeontology, and science communication, 1841 was when Owen coined the “Dinosauria”, tying together disparate forms such as Hylaeosaurus, Megalosaurus and Iguanodon by the recognition that they were not “typical reptiles” but rather advanced in many distinct ways (e.g. locomotor adaptations) that united them as a group. We owe a lot to that early recognition, which was no facile achievement considering how fragmentary most of the early (pre-“Bone Wars”) dinosaur fossil discoveries were. Like Darwin, Owen realized that the giant ground sloths that he described (and Darwin found many of during his Beagle voyage), such as Megatherium, were related animals, too, and in this case having extant relatives.

Most broadly, within comparative biology, Owen searched for the principles of and codified the concept he called homology, which was part of his very French/Germanic quest for “unity of type” as an fairly essentialist (but not always Platonic, as Rupke cautions- pp. 126-7,130), typological (even teleological?) principle underlying common themes in comparative anatomy. His tome on the “archetype” and vertebral components of the skull (see pics above) is lavishly detailed and a challenging but rewarding read, with fascinating (even if sometimes quite wrong) ideas about homologous parts of vertebrate heads. Again, Owen’s work in comparative anatomy easily became an integral part of evolutionary theory– homology as a consequence of (and reciprocally, evidence for) common ancestry featured prominently. As Rupke notes (p.179), “With little more than a flick of the fingers, Owen’s archetype could be turned into an ancestor.”

Tail sheath/club of Meiolania! from Owen, R. (1888). On parts of the skeleton of Meiolania platyceps (Ow.). Philosophical Transactions of the Royal Society of London. B, 181-191. http://www.jstor.org/stable/91676 FREE!

Tail sheath/club of Meiolania! Reminiscent of this…
from
Owen, R. (1888). On parts of the skeleton of Meiolania platyceps (Ow.). Philosophical Transactions of the Royal Society of London. B, 181-191.
http://www.jstor.org/stable/91676 FREE!

Jawsome! Thylacoleo, marsupial lion. From: Richard Owen, Additional Evidence of the Affinities of the Extinct Marsupial Quadruped Thylacoleo carnifex (Owen). Phil. Trans. R. Soc. Lond. B: 1887; 178: 1-3 http://rstb.royalsocietypublishing.org/content/178/1 FREE!

Jawsome!
Thylacoleo, marsupial lion.
From: Richard Owen,
Additional Evidence of the Affinities of the Extinct Marsupial Quadruped Thylacoleo carnifex (Owen).
Phil. Trans. R. Soc. Lond. B: 1887; 178: 1-3
http://rstb.royalsocietypublishing.org/content/178/1 FREE!

This year (2015) is the 350th anniversary of the journal Philosophical Transactions of the Royal Society, in which Owen published key studies of exotic Gondwanan animals such as the giant, tail-clubbed early turtle Meiolania and the “marsupial lion” Thylacoleo (see pics above). Some of Owen’s most outstanding and earliest work, likewise published in Phil. Trans., concerned seemingly aberrant mammals like the platypus (Ornithorhynchus), whose egg-laying and milk-excreting organs he detailed in 1832-1834 (see pics below). Like so many of his discoveries, these detailed descriptions and gorgeous commissioned woodcut illustrations often were sound, groundbreaking work, and are still cited and comprehensible today. Yet Owen’s interpretations sometimes became re-evaluated in a Darwinian rather than transcendentalist light, ironically building the case for Darwinian-style evolution (transmutation). Was the platypus a mammal, reptile or bird? Owen correctly assigned it to the Mammalia and recognized its relationship with the spiny anteaters (echidnas), but today we understand it better as a member of an early branch off the mammalian stem that includes a broad diversity of other species such as the multituberculates. Brian Hall wrote a review of the history of the “platypus paradox” here— it’s a fascinating story.

"Areola" of the female platypus in the abdominal region, with embiggened version below. From: Richard Owen, On the Mammary Glands of the Ornithorhynchus paradoxus. Philosophical Transactions of the Royal Society of London Vol. 122 (1832), pp. 517-538 http://www.jstor.org/stable/107974 FREE!

“Areola” of the female platypus in the abdominal region, with embiggened version below.
From:
Richard Owen, On the Mammary Glands of the Ornithorhynchus paradoxus.
Philosophical Transactions of the Royal Society of London
Vol. 122 (1832), pp. 517-538
http://www.jstor.org/stable/107974 FREE!

Dissection of a female platypus, showing the egg-laying apparatus. From: On the Ova of the Ornithorhynchus paradoxus Richard Owen Philosophical Transactions of the Royal Society of London Vol. 124 (1834), pp. 555-566. http://www.jstor.org/stable/108077 FREE!

Dissection of a female platypus, showing the egg-laying apparatus.
From:
On the Ova of the Ornithorhynchus paradoxus
Richard Owen
Philosophical Transactions of the Royal Society of London
Vol. 124 (1834), pp. 555-566.
http://www.jstor.org/stable/108077 FREE!

As a PhD student of Prof. Kevin Padian, a Richard Owen afficionado and historian, I couldn’t escape awareness of Owen. His visage decorated many parts of Padian’s office and we were often reminded of Owen’s prodigious prowess (and his sly politics- e.g., his “Parthian shot” letter that Padian described). But I didn’t go back and read much Owen until recently, while researching the evolution of the avian patella with my own PhD student Sophie Regnault. Owen described a patella in the moa Dinornis, but we re-interpreted this as an ankle sesamoid bone (common in moa)– although the described fossil “patella” itself seems to have been lost. Then Owen’s patella research came up in a later, often vitriolic, debate (featuring the eminent bird anatomist Shufeldt as well as other scientists Jeffries and Gill) in Science magazine over what bones cormorants and other birds have in their knees– read more about it here. In perusing Owen’s moa and other anatomical work, I gained a deep appreciation for it and now I’m a fan. I even feel a special kinship with Owen– like me, various zoos sent him their specimens for scientific study via dissection, and he was an active science communicator. I’m sure he’d have appreciated my freezers. Not so sure about this blog…

Find the "patella"! From Professor Owen C.B., F.R.S., F.Z.S., &c. (1883), On Dinornis (Part XXIV.): containing a Description of the Head and Feet, with their dried Integuments, of an Individual of the species Dinornis didinus, Owen. The Transactions of the Zoological Society of London, 11: 257–261. http://onlinelibrary.wiley.com/doi/10.1111/j.1096-3642.1883.tb00360.x/abstract FREE!

Find the “patella”!
From Professor Owen C.B., F.R.S., F.Z.S., &c. (1883), On Dinornis (Part XXIV.): containing a Description of the Head and Feet, with their dried Integuments, of an Individual of the species Dinornis didinus, Owen. The Transactions of the Zoological Society of London, 11: 257–261.
http://onlinelibrary.wiley.com/doi/10.1111/j.1096-3642.1883.tb00360.x/abstract FREE!

So that’s my ode to Owen, which lightly touches on highlights of his storied career. Opinions vary on how fun he would have been to quaff pints of ale with (what do you think?), but as fabled (if flawed) heroes of science go, he deserves the label, and morphologists should continue to imbibe and savour his scholarly works, seeking draughts of inspiration within their contents as gourmands of Owen-ia. With some 600 papers published by Owen, there’s surely more for us all to discover.

Morphologists and friends, what’s your favourite Owen paper and why? Speak up!

[If you remain silent, at least do that while reading some Owen today!]

And happy Darwin Day!

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