[insert clever quip about australopithecus hips]

A week and a half ago, Kibii and colleagues (2011) published reconstructions and re-analyses of two hips belonging to the 1.98 million-year old Australopithecus sediba. As with many fossil discoveries, these additions to the fossil record raise more questions than they answer. Unless the question was, “did A. sediba have a pelvis?” It did. Here’s a good summary from the paper itself:

Thus, Au. sediba is australopith-like in having a long superior pubic ramus and an anteriorly positioned and indistinctly developed iliac pillar…[and] Homo-like in having vertically oriented and sigmoid shaped iliac blades, more robust ilia, and a narrow tuberoacetabular sulcus…and the pubic body is upwardly rotated as in Homo. (p. 1410, emphases mine)

So far as I can tell, the main way the hips are ‘advanced’ toward a more human-like condition is that the iliac blades are more upright and sweep forward more than in earlier known hominid hips. Here’s the figure 2 from the paper (more sweet pics of the fossils are available here). NB that in both A. sediba hips much of the upper portions of the iliac blades are missing (reconstructed in white; this region is missing in lots of fossils), so it’s possible they were more flaring like the australopith in the center photo.

The authors’ bottom-line, take-home point is that the A. sediba pelvis has features traditionally associated with large-brained Homo – but belonged to a small-brained species (based solely on the ~430 cc MH1 endocast). They argue that this means that many of these unique pelvic features did not evolve in the context of birthing large-brained babies, as has often been thought. They state that these features are thus “most parsimoniously attributed to altered biomechanical demands on the pelvis in locomotion,” and suggest that this hypothetical locomotion was mostly bipedalism but with a good degree of climbing. Maybe, maybe not. This interpretation is consistent with the analysis of the A. sediba foot/ankle (Zipfel et al. 2011).

The weird mix of ancient (australopith-like) and newer (Homo-like) pelvic features in A. sediba really raises the question of how australopithecines moved around. More intriguing is that the A. sediba pelvis has different Homo-like features than the ~1 million year old Busidima pelvis (Simpson et al. 2008), which has been attributed to Homo erectus (largely in aspects of the iliac blades). This raises the question of whether A. sediba is really pertinent to the origins of the genus Homo, and whether the Busidima pelvis belongs to Homo erectus or a late-surviving robust australopithecus (e.g. boisei, Ruff 2010).

Also interesting is that the subpubic angle (in the pic above, the upside-down “V” created by the pubic bones just above the red labels) is pretty low in MH2. This is curious because modern human males and females differ in how large this angle is – females tend to have a large angle which contributes to an enlarged birth canal, whereas males have a low angle like MH2. But MH2 is considered female based on skeletal and dental size. This raises the additional questions of whether human-like sexual dimorphism had not evolved in hominids prior to 1.9 million years ago, and whether the sex of MH2 was accurately described.

Finally, though the authors did a great job comparing this pelvis with those from other hominids, I think a major, more comprehensive comparative review of hominid pelves is in order. How does the older A. afarensis hip from Woranso (Haile-Selassie et al. 2010) inform australopithecine pelvic evolution? What about the possibly-contemporary-maybe-later hip from the nearby site of Drimolen (Gommery et al. 2002)? Given the subadult status of the MH1 individual, it would be interesting to compare with the WT 15000 Homo erectus fossils, or A. africanus subadults from Makapansgat, to examine the evolution of pelvic growth.

ResearchBlogging.org

Lots of interesting questions arise from these fascinating new fossils. “The more you know,” right?

References
Gommery, D. (2002). Description d’un bassin fragmentaire de Paranthropus robustus du site Plio-Pléistocène de Drimolen (Afrique du Sud)A fragmentary pelvis of Paranthropus robustus of the Plio-Pleistocene site of Drimolen (Republic of South Africa) Geobios, 35 (2), 265-281 DOI: 10.1016/S0016-6995(02)00022-0

Haile-Selassie Y, Latimer BM, Alene M, Deino AL, Gibert L, Melillo SM, Saylor BZ, Scott GR, & Lovejoy CO (2010). An early Australopithecus afarensis postcranium from Woranso-Mille, Ethiopia. Proceedings of the National Academy of Sciences of the United States of America, 107 (27), 12121-6 PMID: 20566837

Kibii, J., Churchill, S., Schmid, P., Carlson, K., Reed, N., de Ruiter, D., & Berger, L. (2011). A Partial Pelvis of Australopithecus sediba Science, 333 (6048), 1407-1411 DOI: 10.1126/science.1202521

Ruff, C. (2010). Body size and body shape in early hominins – implications of the Gona Pelvis Journal of Human Evolution, 58 (2), 166-178 DOI: 10.1016/j.jhevol.2009.10.003

Simpson, S., Quade, J., Levin, N., Butler, R., Dupont-Nivet, G., Everett, M., & Semaw, S. (2008). A Female Homo erectus Pelvis from Gona, Ethiopia Science, 322 (5904), 1089-1092 DOI: 10.1126/science.1163592

Zipfel, B., DeSilva, J., Kidd, R., Carlson, K., Churchill, S., & Berger, L. (2011). The Foot and Ankle of Australopithecus sediba Science, 333 (6048), 1417-1420 DOI: 10.1126/science.1202703

New Australopithecus sediba analyses

A slew of papers analyzing the brain, hands, feet, and pelvis of Australopithecus sediba were just published in the journal Science. I have not had a chance to read them yet – nor will I for a few days as I’m in a wedding Saturday [not mine 😦 ] and the partying starts in a few hours. So I’m afraid I won’t be able to report on and interpret these on the blog for a while. Please stay tuned!

CT reconstruction, from Science (follow link above).
The exact same thing happened to me 2 years ago when the Ardipithecus ramidus skeleton was (finally) published. I remember waiting in the Detroit airport to board a flight to St. Louis to begin my platonic soul-mate’s bachelor party, and I get a flurry of emails on my phone announcing the skeleton in the 15 year old closet.
So media beware – whenever I’m in a wedding, badass new fossil studies will be published. 

eFfing Fossil Friday – Renaissance and Designer Fossils

Sorry I’m a bit late on this one, and that I’ve fallen behind on keeping the blog updated. I’ve been scrambling to make all the observations on, and collect all the data from, these Australopithecus robustus mandibles in a short time. As my advisor likes to remind me, everything always takes 3x longer than you initially anticipate, and this is certainly true of my work here. Yesterday (the actual Fossil Friday), in fact, I probably spent only 30 min with these fossils. Instead, I accompanied Lee Berger and John Hawks on a trip to Malapa – the site that recently yielded fossils of the mysterious Australopithecus sediba – and other sites in the area. To get there, I rented a car and drove on the wrong side of the road for the first time – it was a trippy trip, every time I got in the car I reached to my left for a phantom seat belt, and kept searching for the gear-shift my mind thought was in the door. Nuttiness.
Anyway, I have two thoughts for this edition of eFfing Fossil Friday. First point, related to the great tour from Dr. Berger, is that a ton of hominid fossils are lying in wait for us to re-expose them to the light of day. In South Africa, the classic Plio-Pleistocene sites have been Makapansgat (A. africanus), Sterkfontein (A. africanus) and Swartkrans (A. robustus and early Homo). These sites have variously been worked since the early 20th century. Since then, a number of other hominid-bearing sites – largely in the same area as Sterkfontein and Swartkrans – have been discovered: Gladysvale, Gondolin, Drimolen, and most recently Malapa. Yet still a metric-tonne of work is still being done on the more classic sites (except maybe Makapansgat?).
View of the valley, Malapa is somewhere in the background, I think the green patch of trees near the center, just before the big hill-shadow (?).
But these sites are just the tip of a fossiliferous iceberg. A few years ago when I was working here I accompanied some other researchers on a survey for more fossil sites in the area. What I learned then is that if you look across the Sterkfontein valley in the winter, the dessicated grassland is pimpled with the occasional patch of green trees – these small verdant isles are the tells of underlying cave systems (the caves contain water that plants will cut throats for). What was driven home yesterday at Malapa and other sites Dr. Berger showed us, is that these caves are all over the place, many fossil treasure-troves. What’s more, the A. sediba discovery (and the massive hominid molars from Gondolin) points to the idea that we are only beginning to understand what hominid life was like in the past. There is a rich prehistory still waiting to be discovered in South Africa, and undoubtedly also the rest of the African continent. Human paleontological work is far from exhausted. Let us usher in a Renaissance of field Paleoanthropology!
My next thought is that the process of fossilization can make the fossil-memories of past life quite beautiful. Now, in life the enamel of teeth is white-ish (yellow/brown is also not uncommon), and bone is this off-white/yellowish color. But during the process of fossilization, the original minerals used to make the bone (and less commonly teeth) are replaced by those in the surrounding soil. Often these minerals gussy up the fossils in neat new ways – manganese for example tends to make bone/tooth black.


Check out SK 61, an infant/child Australopithecus robustus. After fossilization, this thing takes on a designer, tortoise-shell coloration (left, above). SK 12, an older adult A. robustus (right, above), is another good example: some subterranean joker has drawn a smiley face beneath his left premolar (circled). So while we are often left with a meager fossil record, at least the fragments we get are voluptuously variegated.