Abstract

Post-cranial differences between extant apes and humans include differences in the length, shape and size of bone elements relative to each other; i.e. differences in proportions. Foot proportions are influenced by the different functional requirements of climbing and bipedal locomotion. Phalangeal length is generally correlated with locomotor behaviour in primates and there is variation in hominins in relative phalangeal lengths – the functional and evolutionary significance of which is unclear and currently debated. Homo naledi has a largely modern rearfoot (i.e. tarsal skeleton) and midfoot (i.e. metatarsal skeleton). The proximal pedal phalanges of H. naledi are curved, but the relative lengths are unknown, because the phalanges cannot reliably be associated with metatarsals, or in many cases even with ray number. Here, we assess the lengths of the proximal pedal phalanges relative to the metatarsals in H. naledi with resampling from modern human and chimpanzee (Pan troglodytes) samples. We use a novel resampling method that employs two boundary conditions, assuming at one extreme that elements in the sample are associated, and at the other extreme that no elements are associated. The associated metatarsophalangeal proportions from digits 1 and 2 are within the 95% confidence interval of the modern human distribution. However, the associated and unassociated proportions from digits 3–5 fall above the 95% confidence interval of the human distribution, but below and outside of the chimpanzee distribution. While these results may indicate fossil preservation bias or other sample-derived statistical limitations, they potentially raise the intriguing possibility of unique medial versus lateral pedal column functional evolution in H. naledi. Additionally, the relevant associated proportions of H. naledi are compared to and are different from those of H. floresiensis. Both species suggest deep phylogenetic placement so the ancestral condition of the pedal phalanges in the genus Homo remains unclear.
 Significance: 
 
 Modern humans demonstrate straight and relatively short pedal phalanges, whereas H. naledi demonstrates curved phalanges of an unknown relative length. This research analyses the relative length of the proximal phalanges to the metatarsals to determine if naledi has relatively short phalanges similar to modern humans or is distinct from modern humans in both its phalangeal length and curvature.
 This analysis further develops a statistical resampling method that was previously applied to large fossil assemblages with little association between bones.

Highlights

  • Evidence of hominin bipedality is obtained from multiple sources: hominin limb proportions from fragmentary postcranial fossil evidence[1]; basicranial position of foramen magnum[2]; preserved fossil partial foot skeletons[3,4,5,6]; and footprints preserved in volcanic ash or lakeshore sediment in eastern Africa at the Laetoli and Ileret sites[7,8,9]

  • If at least one association between the elements was assumed to be present in the fossil sample, the minimum direct proportion of digit 1 fell at the 80th percentile of the modern human cumulative distribution function (CDF) (Figure 3)

  • If there was at least one pair of associated elements in the H. naledi pedal material, we failed to reject the null that H. naledi resembles modern humans in its metatarsophalangeal proportions, those in the medial pedal column

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Summary

Introduction

Evidence of hominin bipedality is obtained from multiple sources: hominin limb proportions from fragmentary postcranial fossil evidence[1]; basicranial position of foramen magnum[2]; preserved fossil partial foot skeletons[3,4,5,6]; and footprints preserved in volcanic ash or lakeshore sediment in eastern Africa at the Laetoli and Ileret sites[7,8,9]. The lateral digits in humans are markedly short compared to those of living great apes, and the lateral toes are much shorter in humans relative to the lengths of the metatarsals.[10,11,12,13] These traits functionally support human bipedal walking and running, including the distinctive ‘toe-off’ phase of the gait cycle.[14,15] Short toes eliminate some of the mechanical costs of walking[16], while a stiff and elongated midfoot (i.e. metatarsal skeleton) is thought to promote the posterior-anterior transfer of weight through the foot’s medial column and from heel-strike to toe-off for a more efficient bipedal gait[11]. We assess proximal phalangeal lengths relative to metatarsal lengths, or the metatarsophalangeal proportions, in the fossil sample of Homo naledi

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