Peering Into Little Foot’s 3.76 Million Year Old Brain

Summary: Researchers create the first endocast reconstruction of nearly the complete brain of the hominin Little Bigfoot. The brain, researchers report, is relatively small and combines both ape like and human like features.

Source: University of Witwatersrand.

First ever endocast reconstruction of the nearly complete brain of the hominin known as Little Foot reveals a small brain combining ape-like and human-like features.

MicroCT scans of the Australopithecus fossil known as Little Foot shows that the brain of this ancient human relative was small and shows features that are similar to our own brain and others that are closer to our ancestor shared with living chimpanzees.

While the brain features structures similar to modern humans – such as an asymmetrical structure and pattern of middle meningeal vessels – some of its critical areas such as an expanded visual cortex and reduced parietal association cortex points to a condition that is distinct from us.

The Australopithecus fossil named Little Foot, an ancient human relative, was excavated over 14 years from the Sterkfontein Caves in South Africa, by Professor Ronald Clarke, from the University of the Witwatersrand (Wits). Its brain endocast was virtually extracted, described and analysed by Wits researcher, Dr Amélie Beaudet, and the Sterkfontein team by using MicroCT scans of the fossil.

The scans reveal impressions left on the skull by the brain and the vessels that feed it, along with the shape of the brain. Beaudet’s research was released as the first in a series of papers planned for a special issue of this journal on the near-complete “Little Foot” skeleton in the Journal of Human Evolution.

“Our ability to reconstruct features of early hominin brains has been limited by the very fragmentary nature of the fossil record. The Little Foot endocast is exceptionally well preserved and relatively complete, allowing us to explore our own origins better than ever before,” says Beaudet.

The endocast showed that Little Foot’s brain was asymmetrical, with a distinct left occipital petalia. Brain asymmetry is essential for lateralisation of brain function. Asymmetry occurs in humans and living apes, as well as in other younger hominin endocasts. Little Foot now shows us that this brain asymmetry was present at a very early date (from 3.67 million years ago), and supports suggestions that it was probably present in the last common ancestor of hominins and other great apes.

Other brain structures, such as an expanded visual cortex, suggests that the brain of Little Foot probably had some features that are closer to the ancestor we share with living chimpanzees.

“In human evolution, when know that a reduced visual cortex, as we can see in our own brain, is related to a more expanded parietal cortex – which is a critical cerebral area responsible for several aspects of sensory processing and sensorimotor integration,” says Beaudet. “On the contrary, Little Foot has a large visual cortex, which is more similar to chimpanzees than to humans.”

Beaudet and her colleagues compared the Little Foot endocast with endocasts of 10 other South African hominins dating between three and 1.5 million years ago. Their preliminary calculation of Little Foot’s endocranial volume was found to be at the low end of the range for Australopithecus, which is in keeping with its great age and its place among other very early fossils of Australopithecus from East Africa.

The study also has shown that the vascular system in Australopithecus was more complex than previously thought, which raises new questions on the metabolism of the brain at this time. This might be consistent with a previous hypothesis suggesting that the endocranial vascular system in Australopithecus was closer to modern humans than it was in the geologically younger Paranthropus genus.

little bigfoot's brain
Virtual rendering of the brain endocast of “Little Foot”. Photo of the original skull by M. Lotter and R.J. Clarke. image is credited to University of Witwatersrand.

“This would mean that even if Little Foot’s brain was different from us, the vascular system that allows for blood flow (which brings oxygen) and may control temperature in the brain – both essential aspects for evolving a large and complex brain – were possibly already present at that time,” says Beaudet.

Given its geological age of over 3 million years, Little Foot’s brain suggests that younger hominins evolved greater complexity in certain brain structures over time, perhaps in response to increasing environmental pressures experienced after 2.6 million years ago with continuing reduction in closed habitats.

“Such environmental changes could also potentially have encouraged more complex social interaction, which is driven by structures in the brain,” says Beaudet.

About this neuroscience research article

Source: Schalk Mouton – University of Witwatersrand
Publisher: Organized by
Image Source: image is credited to University of Witwatersrand.
Original Research: Open access research for “The endocast of StW 573 (“Little Foot”) and hominin brain evolution” by Amélie Beaudet, Ronald J. Clarke, Edwin J. de Jager, Laurent Bruxelles, Kristian J. Carlson, Robin Crompton, Frikkie de Beer, Jelle Dhaene, Jason L. Heaton, Kudakwashe Jakata, Tea Jashaihvili, Kathleen Kuman, Juliet McClymont, Travis R. Pickering, Dominic Stratford in Journal of Human Evolution. Published December 18 2018.

Cite This Article

[cbtabs][cbtab title=”MLA”]University of Witwatersrand”Peering Into Little Foot’s 3.76 Million Year Old Brain.” NeuroscienceNews. NeuroscienceNews, 18 December 2018.
<>.[/cbtab][cbtab title=”APA”]University of Witwatersrand(2018, December 18). Peering Into Little Foot’s 3.76 Million Year Old Brain. NeuroscienceNews. Retrieved December 18, 2018 from[/cbtab][cbtab title=”Chicago”]University of Witwatersrand”Peering Into Little Foot’s 3.76 Million Year Old Brain.” (accessed December 18, 2018).[/cbtab][/cbtabs]


The endocast of StW 573 (“Little Foot”) and hominin brain evolution

One of the most crucial debates in human paleoneurology concerns the timing and mode of the emergence of the derived cerebral features in the hominin fossil record. Given its exceptional degree of preservation and geological age (i.e., 3.67 Ma), StW 573 (‘Little Foot’) has the potential to shed new light on hominin brain evolution. Here we present the first detailed comparative description of the external neuroanatomy of StW 573. The endocast was virtually reconstructed and compared to ten southern African hominin specimens from Makapansgat, Malapa, Sterkfontein and Swartkrans attributed to Australopithecus and Paranthropus. We apply an automatic method for the detection of sulcal and vascular imprints. The endocranial surface of StW 573 is crushed and plastically deformed in a number of locations. The uncorrected and therefore minimum cranial capacity estimate is 408 cm3 and plots at the lower end of Australopithecus variation. The endocast of StW 573 approximates the rostrocaudally elongated and dorsoventrally flattened endocranial shape seen in Australopithecus and displays a distinct left occipital petalia. StW 573 and the comparative early hominin specimens share a similar sulcal pattern in the inferior region of the frontal lobes that also resembles the pattern observed in extant chimpanzees. The presumed lunate sulcus in StW 573 is located above the sigmoid sinus, as in extant chimpanzees, while it is more caudally positioned in SK 1585 and StW 505. The middle branch of the middle meningeal vessels derives from the anterior branch, as in MH 1, MLD 37/38, StW 578. Overall, the cortical anatomy of StW 573 displays a less derived condition compared to the late Pliocene/early Pleistocene southern African hominins (e.g., StW 505, SK 1585).

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