As for work – I’ve learned loads, and there’s months of work I could do just at Florisbad. Sadly I didn’t get to the fossils, but I’m so swamped with living bovids (and I’m not doing bovines, true cows, so Pelorovis wouldn’t really apply anyway) it’s hard to know what portion of fossil-studying to carve off. As it is, I’m taking some 20-32 measurements, 55+ notes on sutures, notes on dentition, and 4-8 photos per specimen (if available – some are partial or broken skulls, etc.) That’s a ton, though I have extreme difficulty imagining paring back. If anything I may try to swap out photos for the suture notes – see if I can get them from photos later.
But it’s been really exciting to see how just a couple of the different tribes differ in their suture fusion patterns – among adults, and also as it happens through developing juveniles. The patterns and trends aren’t watertight – there’s a lot of variation, and I’m sure I’ll encounter more, but I’m starting to get a picture of it for some taxa, and it varies consistently among the tribes.
To talk more concretely (on the off chance you’re dying to know…) it’s really interesting how, for example, in eland and kudu, the skulls start out with these really large gaps between some of the bones, and then how these gaps close, and stitch together, and then get remodeled by bone maintenance till you can’t see them in the adults – you’d be hard pressed to know that there were originally two bones there. But it doesn’t happen for all sutures that way, and when it does, the timing of it depends on the suture, and on the species. In the kudu and eland, the suture down the midline of the skull (between the left and right frontal bones, which the horns grow on) disappears lickety-split. And the suture it connects to at a right angle, between the frontal and parietal bones (parietals are right behind the frontals, also part of the skull dome, so you get a T-shaped intersection just behind the horns), also disappears lickety-split, but reappears on the side of the head, below the horns, just before it gets to the temporal bone. Chock it up to horns? Naw – the hornless female kudu do it too. And the heavily-horned Hippotragines (sable, gemsbok, roans) and some of the larger Reduncines (waterbuck, lechwes) have totally visible F-F and F-P sutures all the time, no hint of remodeling them out of existence. And trust me, some of the skull+horns of each of these groups are very heavy – it’s not a product of horn size, that’s for sure. Move to the smaller blesbok (Alcelaphines), and you get juveniles whose F-F suture goes from open and simple at the nasal bones, to zig-zagged and smooth between the eyes, to crazily complex between the horns with big gaps between fine struts of bone in the midst of being fused and remodeled like mad, and by the time it gets to the parietal bone, its already being remodeled and turned invisible. This is in the span of about 5-6 inches. Crazy! And – why??
And I haven’t even gotten to the wildebeest or the teeny tiny dik-diks and duikers yet. But from a couple casual looks, the teeny tiny ones don’t seem to reach the remodeling stage for any major suture, even when they start hyper-ossifying their craniums. (I’ve got a couple cool pictures of these tiny skulls with loads of extra bone deposited in quasi-random patterns on the forehead and vicinity – like lace or an incipient coral reef. For their size, it’s clear these skulls weigh a fair bit more than your typical midget bovid skull). The bones just come together, sit in place, the line remains visible and uncomplicated, and that’s that – you’ve got a skull that stays together and does what it’s supposed to do, even when the “make more bone!!!” switch has been turned on, as with the lace-headed bovidettes. This is interesting because - if that generalization about the small guys holds true, and I connect the dots well enough (and that’s a fair task) - it suggests how the little guys grow to little sizes, and the big guys grow to big sizes – because there are a couple of options for how to do it, and how one achieves X size can, like most other traits, give clues to evolutionary pathways taken, and relationships (both historical and current) among species.
How does one become small (that is, become smallER compared to an ancestral stock)? Assuming a rubric of typical development – that is, the ancestral stock had a typical growth trajectory of small baby to big(ger) adult, and adults look characteristically different than the babies (pretty safe assumptions here) - what are your options? Well, you can either slow down your rate of growth while zooming through the steps to maturity, basically ending up as a miniature version of the ancestral adult. Alternatively, you can keep growth rates similar and just stop development earlier (save some key reproductive changes for sexual maturity), which results in comparatively infantile looking adults. (Something along this line is hypothesized to have happened in human evolution – the quick rationale or explanation is: just look at a baby chimp; in terms of proportions, we look a lot more like a baby chimp than an adult chimp, which of course assumes our common ancestor looked kind of chimp-like; there are probably better, and worse, descriptions of this unknown ancestor). Of course, those are two extremes of a continuum, and in most cases there’s probably a mix. But it’s good for keeping peas and carrots straight in your mind.
What about for getting big? Same idea – you can simply increase the rate of growth, while keeping the same sequence of steps to looking like an adult – they’re just stretched out in terms of the number of pounds or inches between each step. Or, you can add steps, so that you zoom past the previous “adult” form and achieve something relatively new (or do a combination).
How’s this possible? Well, the simplest way is to just extend the duration of the developmental program – that is, some parts of your body (in my case, I’m interested in heads) grow faster than other parts,or grow in this direction vs. that, (and at different times to boot). Thisresults in changes in the proportions of that body part. If you just think about these as basic instructions (“grow this region of the bone a third faster than that region”) there’s no built-in stopping point. The halt signal comes from elsewhere in the body or program. So if you change the timing of that halt signal, you’re going to get a head shaped a bit differently than normal. That’s all. Do it just a smidge, and a scientist probably won’t even notice, or will chock it up to “normal variation.” Do it a lot, and they start to take notice. Do it repeatedly over tens of millions of years, and some people will say you were deposited on earth as-is a few thousand years ago.
Of course, adding genuinely “new” traits (new instructions for development) is very interesting, and more complicated (“new” being completely relative and contextual, and on the whole a misleading but common word). And on that reason alone, it’s reasonable to think it happens less often. So, my strategy is to keep a good eye out for the things most likely to happen, and among those cases, keep another eye out for oddballs, and see if and how they might go together. Because, given the fact of inheritance, systematic widespread features don’t just come out of left field, although history has a nasty habit of deleting the data that would make that obvious. I mean, when you get down to it, nothing comes out of left field, even the unpredictable congenital defects, “monstrosities” and the like – it’s just unexpected (to us) given a backdrop of experience. If one knew about the genetic abnormality prior to it being obvious, then the resulting abnormality would not be “new,” left-field, or spontaneous – we’d view it as the result of a known cause. That is, stuff acting in accordance with its identity (in this case, dynamic, organic, biological stuff, but still stuff just the same). The gambols of evolution are no less causeless, but a trifle more cumbersome to nail down, given the number of things involved, the time involved, and the patchiness of the data (and several orders of magnitude fewer people working on such questions as compared to, say, biomedical research).