Remember this broken Giraffatitan dorsal vertebra, which Janensch figured in 1950?

It is not only cracked in half, anteroposteriorly, it’s also unfused.

Here’s a better view of the broken face, more clearly showing that the neural canal is (a) much taller than wide – unlike all vertebrate spinal cords – and (b) almost entirely situated ventral to the neurocentral joint, getting close to the condition in the perverted Camarasaurus figured by Marsh.

Here’s a dorsal view, anterior to the top, with Mike’s distal forelimbs for scale.

Left lateral view.

Right lateral view – note the subtle asymmetries in the pneumatic foramen/camera. A little of that might be taphonomic distortion but I think much of it is real (and expected, most pneumatic systems produce asymmetries).

And postero-dorsal view, really showing the weird neural canal to good advantage. In this photo and in the pure dorsal view, you can see that the two platforms for the “neural arch” – which, as in the aforementioned Camarasaurus, is neither neural nor an arch – converge so closely as to leave only a paper-thin gap.

A few points arise. As explained in this post, it makes more sense to talk about the neurocentral joint migrating up or down relative to the neural canal, which is right where it always is, just dorsal to the articular faces of the centrum.

So far, in verts I’ve seen with “offset” neurocentral joints, the joint tends to migrate dorsally in dorsal vertebrae, putting the canal inside the developmental domain of the centrum (which now includes a partial or total arch in an architectural sense, even though the chunk of bone we normally call the neural arch develops as a separate bit) – as shown in the first post in this series. In sacral and caudal vertebrae, the situation is usually reversed, with the joint shifted down into what would normally be the centrum, and the canal then mostly or completely surrounded by the arch – as shown in the second post in the series. This post then doesn’t really add any new concepts, just a new example.

Crucially, we can only study this in the vertebrae of juveniles and subadults, because once the neurocentral joints are fused and remodeled, we usually can’t tell where the old joint surface was. So it’s like cervicodorsal and caudal dorsal pneumatic hiatuses, in that the feature of interest only exists for part of the ontogeny of the animal, and our sample size is therefore inherently limited. Not necessarily limited by material – most museums I’ve visited have a fair amount of juvenile and subadult material in the collections – but limited in published visibility, in that for many sauropods only the largest and most complete specimens have been monographically described.

So once again, the answer is simply to visit collections, look at lots of fossils, and stay alert for weird stuff – happily, a route that is open to everyone with a legitimate research interest.


  • Janensch, W. 1950. Die Wirbelsaule von Brachiosaurus brancai. Palaeontographica (Suppl. 7) 3:27-93.

Illustration talk slide 39

Illustration talk slide 40

Illustration talk slide 41

Illustration talk slide 42

Illustration talk slide 43

The Sauroposeidon stuff is cribbed from this post. For the pros and cons of scale bars in figures, see the comment thread after this post. MYDD is, of course, a thing now.

Previous posts in this series.


Wedel, M.J., and Taylor, M.P. 2013. Neural spine bifurcation in sauropod dinosaurs of the Morrison Formation: ontogenetic and phylogenetic implications. Palarch’s Journal of Vertebrate Palaeontology 10(1): 1-34. ISSN 1567-2158.

From the collections of the American Museum of Natural History, I give you the sacrum and fused ilia of “Apatosaurusminimus AMNH 675, as correctly identified by Steve P in a comment to the previous post:

"Apatosaurus" minimus sacrum with fused ilium, right lateral view

As Steve P rightly pointed out, AMNH 675 was designated as Brontosaurus sp. by Osborn (1904), and made the type of Apatosaurus minimus by Mook (1917).

It’s been known for some time that whatever this is, it’s not Apatosaurus — see for example McIntosh (1990a:398), McIntosh (1990b:59) and Upchurch et al. (2004:298). But what actually is it? Well, at the moment, no-one knows. Matt and I now have a manuscript in prep that we hope will somewhat elucidate this question. More to come on this specimen, most likely.


McIntosh, John S. 1990a. Sauropoda. In The Dinosauria, pp. 345–401. Berkeley and Los Angeles: University of California Press.

McIntosh, John S. 1990b. Species Determination in Sauropod Dinosaurs with Tentative Suggestions for the Their Classification. In Dinosaur Systematics: Approaches and Perspectives, pp. 53–69. Cambridge: Cambridge University Press.

Mook, Charles C. 1917. Criteria for the determination of species in the Sauropoda, with description of a new species of Apatosaurus. Bulletin of the American Museum of Natural History 38:355-360.

Osborn, Henry F. 1904. Manus, sacrum, and caudals of Sauropoda. Bulletin of the American Museum of Natural History 20:181-190.

Upchurch, Paul, Paul M Barrett, and Peter Dodson. 2004. Sauropoda” In The Dinosauria, 2nd Edition, pp. 259–322. Berkeley and Los Angeles: University of California Press.

A couple of posts back, when Matt was talking about turtle laminae, he included a photo of me in front of the skeleton of the giant turtle Archelon. Also in that photo is the tripod I was using — if you want to call it that — a tripod of altogether startling inadequacy. Here it is again, this time in the collections of the AMNH:

(Bonus SV-POW! points for anyone who can tell me what taxon or specimen I am working on. Sorry, Heinrich, you’re disqualified, since you already know.)

Why did we use such a poor tripod? Matt was planning to bring a proper one, but at the last minute decided to downsize his luggage by taking one small enough to fit into a smaller bag — in fact, it’s the tripod that came free with a telescope he recently bought. Not a good move: it was too short for many of the shots we wanted to take, too flimsy to properly stabilise the camera in many situations, and didn’t have enough degrees of freedom to let us get every shot we wanted from the best position.

Still, it was better than nothing, and we did contrive to get all the specimen photos we needed.

At the end of the week, when we finished up in collections and went to catch our taxi to the airport, Matt left the tripod behind. I emailed our AMNH host Carl Mehling to explain:

Matt deliberately left behind his tripod — it’s on the desk where we had the pelvic elements. He has much better tripods at home, and regrets the false economy of bringing that lighter and less stable one. But we figured it would be better than nothing for the use of anyone who turns up in collections with no tripod at all, so please feel free to make it available to visitors. Matt asks only that it be known as “The Mathew J. Wedel Memorial Tripod”.

Carl replied:

Thanks so much for the tripod – I KNOW it will come in handy!

My response:

Ah, sorry about this but my client insists that it must be known by its full title The Mathew J. Wedel Memorial Tripod at all times. If necessary, you may abbreviate it to TMJWMT on second and subsequent mentions.

Carl’s reply:

I can engrave it in the Lab and apply a B72/India Ink/B72 sandwich acronym/monogram on it. I will also construct an archival museum mount for it and put a security chip in its brain.

That’s when Matt himself weighed in:

Oh, and be sure that when the tripod is not in use it is stored in an airtight positive pressure chamber full of an inert gas. It should also be polished twice daily with the down of a hatchling bald eagle (fresh down each time, naturally). Finally, the tripod itself should be listed as an author on any publications that include photos taken with it. Please send a runner to my office in California to confirm that these instructions will be carried out to the letter.

The runner hasn’t arrived yet (to my knowledge) but I think we can take it as read that Carl will comply with these very reasonable conditions.

So, folks! If ever you’re working in the AMNH big-bone room, and you find you’ve forgotten your tripod … you might just be lucky enough to be allowed use of the Mathew J. Wedel Memorial Tripod!

Sometimes you just can’t make this stuff up.

You may recall a story from the Onion Our Dumb Century book, allegedly from 1904, about the skeleton of Satan being discovered in Wyoming. Mike used his occult powers to put together this scan from freely available online sources:

If you scrutinize the above image carefully, you’ll see that ‘Satan’ is an Allosaurus (I’m no theropod booster, but I always thought that was a little harsh on T. rex).

Why am I telling you this? Because last week Mike and I were toiling in the big bone room in the basement of the AMNH when we came across AMNH 666.

It’s an ilium. (Of course it would have to be an appendicular element. Vertebrae are from on high [or dorsal, if you prefer].)

Of Allosaurus!

The stomach-churning color here could be a manifestation of diabolical power, or just what happens when you try to photograph a pink specimen label on a yellow-orange forklift.

After this harrowing encounter, we cleansed our bodies, minds, and souls with street-vendor hot dogs and The Avengers.* That particular mode of exorcism may not be the most effective–I felt distinctly dodgy that evening. But the next day we received illumination at the Altar of Sauropod Awesomeness and were soon back to what we jokingly refer to as normal.

* The best way to see The Avengers is by going up to the observation deck of the Empire State Building shortly beforehand, so big swathes of the Manhattan skyline will still be in your mental RAM during the big final battle. I understand it’s not an option for everyone.

Mike gets a shot of a sauropod sacrum in the AMNH basement.

…with sauropod bones!

Lots of basements have them. Some basements have had them for decades, and other basements have been newly constructed to house them. So you can take advantage of that retro chic while taking your basement into the 21st century!

What the heck am I talking about?

Matt ponders the mysteries of evolution in the AMNH basement.

One of the nifty features of WordPress is that you can track the search terms that people are using to find your blog. After Mike put up his “Suboptimal location of Mamenchisaurus” post, we noticed that one of the top search terms bringing people to SV-POW! was ‘basement’. Yeah, that’s right, ‘basement’. In fact, ‘basement’ is the 5th highest search term of all time that has brought people to SV-POW! And that’s not unusual–in fact, of the top 5 search terms bringing people here, only one is sauropod-related (Brachiosaurus, at number 2).

As of this posting, here are the Top 10 non-sauropod search terms of all time that have led people to SV-POW!, listed by rank, and including the number of hits in parentheses:

1. rabbit (18,235)

3. leopard seal (12,797) — this explains why “Sorting out Cetiosaurus nomenclature”, which even Mike admits is the most boring topic we’ve ever covered here, is the 11th most popular post of all time on this blog!

4. flamingo (10,974)

5. basement (9743)

12. twinkie (3434)

14. flamingos (3102) — double dipping for the “Necks lie” post!

20. pig skull (2099)

21. savannah monitor (2078)

22. varanus exanthematicus (1936) — double dipping for “Four complete, articulated, extant sauropod skeletons–yes, really!”

24. shish kebab (1660) — double dipping for “Sauropods were corn-on-the-cob, not shish kebabs”.

Mike and Darren discover a new dwarf sauropod in the basement at Oxford.

We’re apparently getting a lot of hits from people who want to remodel their basements. I’m all for that (the remodeling, and the extra hits), so I’m embracing it. You want basements, we got ’em. We’ll drown you in pictures of sauropod vertebrae in basements. Did I say basement? Basement, basement, basement!

(Why am I pushing basement and not rabbit, flamingo, or leopard seal? Partly because basement used to be our number 1 search term and I want to see its fortunes rise again. Partly because those other things are at least biological, and it cracks me up to have a common architectural term bringing people to the blog. And partly because I want to upstage John and his freezers.)

Basement Renovation Instructions

This short guide will help you with your project.

Is your basement in a museum?

If YES, then:

1. Fill it with sauropod vertebrae.

2. Call us.

If NO, then:

1. Fill it with anything you like except sauropod vertebrae.

2. Support your local museum.

Don’t forget: basement!

I only became aware of the term Academic Spring the other day but I instantly loved it. The OA wars have heated up significantly in the past few weeks, and Academic Spring crystallizes a lot of what is going on.

Although we always welcome new readers, and no-one who cares about science can afford to be ignorant about access to scholarly publications, we do sometimes feel that at SV-POW! we are mostly preaching to the converted. But access is not just a problem for scientists and academics, it’s a problem for everyone, including physicians, patient groups, engineers, small business owners, students, and, frankly, anydamnbody who wants to inspect the fruits of the research their taxes paid for. So it’s important to get the message out, broadly, to the most people possible, in as many venues as possible, until Joe and Jane Citizen get mad enough about the situation to demand better behavior by their elected representatives and better service from the corporations that allegedly have their interests at heart.

To that end, Mike has a new piece up at The Independent today. Because he couldn’t assume that his readers would be familiar with the OA wars or Academic Spring, he had to lay out the whole case in a limited number of words. I think he did a bang-up job. Because the piece is so self-contained (although it has some choice links that are worth following up), it serves as a front-line report for those of us familiar with the OA wars, and a solid overview for everyone else. Go check it out.

Finally, since you haven’t gotten a lot of sauropod action lately, here are some small Giraffatitan humeri in the basement of the  Museum für Naturkunde with Vanessa Graff for scale. You can tell these are small ones because they’re Vanessa-sized or smaller; the big ones are taller than I am…and they’re still from subadults. Must blog sometime about the awesomeness of the basement full o’ sauropods at the MfN, but not today. Excelsior!

Hello again, old friend

December 5, 2011

This week the SV-POW!sketeers are off to Bonn, Germany, for the Second International Workshop on Sauropod Biology and Gigantism. All three of us will be there, plus SV-POW! guest blogger Heinrich Mallison, plus Wedel Lab grad student Vanessa Graff, plus about 50 other awesome scientists from around the world. So we’ll have a ton of fun, but we probably won’t get much posted.

In the meantime, enjoy this cool encounter from the bone cellar at the Humboldt Museum in Berlin, where Mike and I fetched up at the end of the last IWSBG back in 2008. It’s a transversely-sectioned dorsal centrum of Giraffatitan, one that Janensch illustrated in his 1950 monograph on the vertebrae of Giraffatitan. Mike and I were very familiar with the cross-section image from the paper, so it was cool and a bit unreal to find the actual item.


Janensch, Werner. 1950. Die Wirbelsaule von Brachiosaurus brancai. Palaeontographica (Suppl. 7) 3:27-93.

Vanessa Graff and I spent yesterday working in the herpetology and ornithology collections at the Natural History Museum of Los Angeles County (LACM). The herpetology collections manager, Neftali Comacho, pointed us to this skull of Alligator mississippiensis. It’s not world’s biggest gator–about which more in a second–but it’s the biggest I’ve seen in person. Normally it lives in a big rubbermaid tub in the collections area, but this Sunday it will be out on display for Reptile and Amphibian Appreciation Day (RAAD) at the LACM. RAAD will include guest talks, tours of the collections, and live animal demonstrations. If you’re in SoCal and you’re into herps–or have kids, grandkids, nephews or nieces that are into herps–it will be well worth checking out. While you’re there, don’t neglect the newly renovated Age of Dinosaurs and Age of Mammals halls, which are frankly phenomenal: spacious, well-lit, loads of actual material on display, skeletons you can walk all the way around, informative but unobtrusive signage, tasteful integration with existing architecture…I could go on. Better if you just go and see for yourself.

About that gator. First the bad news.  It came to the LACM from another collection, and has no data–no locality, no date collected, nothing. The skull is also missing all of its teeth, the left retroarticular process, the back end of the braincase and the occipital condyle. I think the latter losses were probably caused by a foramen of Winchester.*

Now, the awesome news. The length from the snout tip to the end of the articulars was 680mm and from the snout to the end of the quadrates was 590mm. Irritatingly I did not get a dorsal head length, which is the gold standard for comparative croc skull measurements, because I only reread Darren’s giant croc skull post after I got home last night. Going from the photos, I think the dorsal head length was right around 50 cm (beware, the yardstick in the photos is marked off in inches).

Darren’s post led me to this one, which has some very useful measurements (yay!) of giant croc skulls. The table at the end of that post lists alligator skulls with dorsal head lengths of 58, 60, and 64 cm, so the big LACM gator is nowhere near being the world’s largest. In fact, the 64 cm skull would be a quarter again as large, which is a truly horrifying thought. Still, it’s a big damn skull from a big damn gator.

You might get the impression that here in the Wedel lab we are shamelessly obsessed with giant saurians. And that is in fact true. But we also look at tiny ones, too. Here I’m playing with the skull of a little Tomistoma, the false gharial. Tomistoma is notable because another individual of the genus produced the longest skull of any known extant crocodilian–a whopping 84 cm dorsal head length (photos of this monster are in both of the giant croc skull posts linked above).

The moral of the story? If the sign says don’t go swimming, don’t go swimming. Go to RAAD instead, and see the giant alligator skull, and a ton of other cool stuff besides. And if you’re into gator skulls or just like geeking out on awesome anatomy, check out the 3D Alligator Skull site, a joint project of the Holliday lab and Witmer lab. Have fun!

* bullet hole

When you last saw this rhea neck, I was squeezing a thin, unpleasant fluid out of its esophagus. Previous rhea dissection posts are here and here; you may also be interested in my ratite clearing house post.

We did that dissection back in 2006. Since then I finished my dissertation, got a tenure-track job, and moved twice. The rhea neck followed me, living in a succession of freezers until last spring.

Last spring I thawed it out, straightened it (it had been coiled up in a gallon ziploc), refroze it, and had it cut in half sagittally with a bandsaw. I did all of this for a project that is not yet ready to see the light of day, but there’s a ton of cool morphology here that I am at liberty to discuss, so let’s get on with it.

Throughout the post, click on the images for full resolution, unlabeled versions.

In the image above, you’ll notice that the saw cut was just slightly to the left of the midline, so that almost the entire spinal cord was left in the right half of the neck (the one toward the top of the image; the left half, below, is upside down, i.e. ventral is towards the top of the picture). The spinal cord is the prominent yell0w-white stripe running down the middle of the hemisectioned neck. It’s a useful landmark because it stands out so well. Dorsal to it are the neural arches, spines*, and zygapophyses of the vertebrae, and epaxial muscles; ventral to it are the vertebral centra and the hypaxial muscles.

* If you want to call them that–some of them are barely there!

Here’s the large supraspinous ligament (lig. elasticum interspinale), which is similar to the nuchal ligament of mammals but independently derived. Compare to the nuchal ligament of a horse (image borrowed from here):

Note how the actual profile of the neck is vastly different from what you’d suspect based on the skeleton alone. This is one of the reasons that necks lie. For more on the supraspinous ligament in rheas and its implications for sauropods, see Tsuihiji (2004) and Schwarz et al. (2007).

Birds also have very large interspinous ligaments (lig. elasticum interlaminare), each of which connects the neural spines of two adjacent vertebrae. In the above photo, the blunt probe is passing under (= lateral to) the unpaired, midline interspinous ligament. Rheas are unusual among birds in having such a large supraspinous ligament, and you can see that this interspinous ligament is almost as big. If you tear down the neck of a chicken or turkey, you will find huge interspinous ligaments, and the supraspinous ligament will be tiny if you can identify it at all.

Here’s something I don’t think we’ve ever shown before here on SV-POW!: a photograph of an actual pneumatic diverticulum. That’s the dark hole in the middle of the photo. You can see that we’re in the left half of the neck, lateral to the spinal cord, almost to the postzygapophysis, the articular surface of which is more lateral still (“below” or “deep to” the surface you see exposed in this cut). Usually at each intervertebral joint there is a connection between the lateral pneumatic diverticula that run up the side of the cervical column and pass through the cervical rib loops and the supramedullary diverticula that lie dorsal to the spinal cord inside the neural canal. That connecting diverticulum is the one exposed here.

NB: diverticulum is singular, diverticula is plural. There are no diverticulae or, heaven forbid, diverticuli, although these terms sometimes crop up in the technical literature, erroneously. (I hesitate to point this out, not because it’s not important, but because I’ll be lucky if I didn’t screw up a Latin term elsewhere in the post!)

Here are pneumatic diverticula in a transverse CT section of an ostrich neck (Wedel 2007b: fig. 6; compare to Wedel 2003: fig. 2, another slice from the same neck). In this view, bone is white, muscles and other soft tissues are gray, and air spaces are black. A, lateral diverticula running alongside the vertebral centra. B, air spaces inside the bone. C, supramedullary airways above the spinal cord. This section is close to the posterior end of a vertebra; the flat-bottomed wing-like processes sticking out to either side are the anterior portions of the postzygapophyses. If the slice was a few mm more posterior, we would see the prezygapophyses of the preceding vertebra in contact with them. Also, the vertical bars of bone connecting the centrum to the postzygs would pinch out, and we’d see the diverticula connecting the lateral (A) and supramedullary (C) airways–that’s the diverticulum revealed in the photo two images up.

Here’s another cool section showing a diverticulum and some muscles. Note the short interspinous muscles, which connect the neural spines of adjacent vertebrae. The probe indicates another open diverticulum, and the very tip of the probe is under one of the very thin layers of epithelium that line the diverticula. You can see that this diverticulum lies on the dorsal surface of the vertebra, posterior to the prezygapophysis and anterior to the neural spine. This supravertebral diverticulum is near and dear to my heart, because I have published an image of its traces before.

Lots going on in this photo (remember that you can click for an unlabeled version). This is a middle cervical vertebra of an emu, in anterodorsal view, with anterior towards the bottom of the picture. Bonus geek points if you recognized it as the basis for Text-fig. 9 in Wedel (2007a). I published this photo in that paper because it so nicely illustrates how variable the skeletal traces of pneumaticity can be, even from left to right in a single bone. On the right side of the photo (left side of the vertebra), the bone resorption adjacent to the supravertebral diverticulum produced a pneuamtic fossa, but one without distinct bony margins or a pneumatic foramen. On the other side, the fossa contains a pneumatic foramen which communicates with the internal air spaces, but the fossa is otherwise identical. Fossae like the one on the right are a real pain in the fossil record, because they might be pneumatic, but then again they might not be; such shallow, indistinct fossae can house other soft tissues, including cartilage and fat. This is what I was talking about when I wrote (Wedel 2009: p. 624):

If progressively more basal taxa are examined in the quest to find the origin of PSP [postcranial skeletal pneumaticity], the problem is not that evidence of PSP disappears entirely. It is that the shallow, unbounded fossae of basal dinosaurs are no longer diagnostic for pneumaticity.

For more on that problem, see Wedel (2007a) and the post, “X-Men Origins: Pneumaticity”.

The other labelled bits in the above photo are all muscle attachment points, and you may find Wedel and Sanders (2002), especially Fig. 2, a useful reference for the rest of the post. The dorsal tubercles, or epipophyses, are rugosities dorsal to the postzygapophyses that anchor most of the long, multi-segment epaxial muscles, which in birds are the M. longus colli dorsalis, which originates on the anterior faces of the neural spines, and M. ascendens cervicalis, which originates on the cervical rib loops. The crista transvers0-obliqua is a low, bony crest connecting each dorsal tubercle to the neural spine; it corresponds to the spino-postzygapophyseal lamina (SPOL) of sauropods (see Tutorial 4: Laminae!), and anchors the Mm. intercristales, a group of short muscles that span the cristae of adjacent vertebrae, like the Mm. interspinales only more lateral.

The carotid tubercles serve as points of origin for the M. longus colli ventralis, one of the largest and longest of the multi-segment hypaxial muscles; they have no obvious homolog or analog in sauropods. The lack of this feature might indicate that the hypaxial muscles were less of a big deal in sauropods, for whom lifting the neck was presumably a bigger problem than lowering it. Alternatively, the M. longus colli ventralis of sauropods might have attached to the medial sides of the parapophyses and the capitula of the cervical ribs, which tended to be larger and more ventrally-directed than in basal sauropodomorphs and theropods.

The unlabeled red arrows mark the lateral tubercles and crests of the cervical rib loop, to which we will return momentarily.

Here you can see a big bundle of long epaxial muscles, including both the M. longus colli dorsalis and M. ascendens cervicalis, inserting on the left dorsal tubercle of the vertebra on the right.  Note that the cut here is quite a bit lateral of the midline, and actually goes through the lateral wall of the neural canal in the vertebra on the right (that vert is the fifth back from the front of the section of neck featured in this post, which is incomplete). That is why you see the big, multi-segment muscles here, and not the shorter, single-segment muscles, which lie closer to the midline.

Here are some more muscle attachment points in a bird vertebra (a turkey this time, courtesy of Mike). The lateral crests and tubercles (tubecula ansae and cristae laterales, if you’re keeping track of the Latin) are the same bony features indicated by the red arrows in the photo of the emu vertebra up above. They anchor both the long M. ascendens cervicalis, which inserts on the dorsal tubercles of more anterior vertebrae, and the short Mm. intertransversarii, which span the cervical rib loops of adjacent vertebrae. Sauropods usually have at least small rugosities on their diapophyses and the tubercula of their cervical ribs (which articulate with the diapophyses) that probably anchored homologous muscles.

Here’s a dorsal tubercle above the postzyg on the neural arch of a juvenile Apatosaurus (cervical 6 of CM 555, shown in right lateral view). Notice that the spinopostzygapophyseal lamina (SPOL) and postzygodiapophyseal lamina (PODL) actually converge on the dorsal tubercle rather than on the postzyg. This is pretty common, and makes good mechanical sense.

Dorsal tubercles again, this time on the world’s most wonderful fossil, cervical 8 of the HM SII specimen of Giraffatitan brancai, in the collections of the Humbolt museum in Berlin. While you’re here, check out the pneumato-riffic sculpting on the lateral faces of the neural arch and spine, and the very rugose texture on the tip of the neural spine, SPOLs, and dorsal tubercles. In fact, compare the numerous pocket-like external fossae on this vertebra with the internal air cells exposed in the cross-sectioned rhea neck. I have argued here before that sauropod cervical vertebrae are pretty similar to those of birds; the main differences are that the cervical rib loops are proportionally much smaller in sauropods, and sauropod vertebrae mostly wore their pneumaticity on the outside.

Farther anteriorly in the neck–the three vertebrae pictured here are the third, fourth, and fifth (from right to left) in this partial neck–and somewhat closer to the midline. Now you can see some short epaxial muscles, probably Mm. intercristales and Mm. interspinales (the two groups grade into each other and are often not distinct), spanning adjacent vertebrae. As in several previous photos, the supravertebral diverticulum is visible, as well as the communicating diverticulum that connects the lateral diverticula to the supramedullary airways. I forgot to label them, but ventral to the centra you can see long, light-colored streaks running through the hypaxial muscles. These are the tendons of the M. longus colli ventralis, and in some of the previous photos you can see them running all the way to their origination points on the carotid tubercles. These extend posteriorly from the short cervical ribs of birds, and are homologous with the long cervical ribs of sauropods.

That’s all I have for this time. If you’d like to see all of this stuff for yourself, turkey necks are cheap and big enough to be easy to work with. Geese are good, too. You can see all the same bits in a chicken or a duck, it’s just harder because everything is smaller (if you’re a real glutton for punishment, try a Cornish game hen).

When I first started working on sauropods, their cervical vertebrae made no sense to me. They were just piles of seemingly random osteology. The first time I dissected a bird neck was an epiphany; ever since then, it is hard for me to look at sauropod vertebrae and not see them clad in the diverticula and muscles that shaped their morphology. Go have fun.