Mandibular evidence supports Homo floresiensis as a distinct species

Henneberg et al. (1) and Eckhardt et al. (2) present another pathology-based alternative to the hypothesis that the “hobbit” fossils from Liang Bua, Indonesia, represent a distinct hominin species, Homo floresiensis. They contend that the Liang Bua specimens are the remains of small-bodied humans and that the noteworthy features of the most complete specimen, LB1, are a consequence of Down syndrome (DS). Here, we show that the available mandibular evidence does not support these claims.

Absence of chins in the two mandibles recovered at Liang Bua, LB1 and LB6, is a key issue (1, 3). That these specimens lack chins has been argued to preclude their attribution to Homo sapiens, because a chin is widely accepted to be a defining characteristic of our species (3). Henneberg et al. reject this argument on the grounds that a chin is often absent in living Australo-Melanesians. However, the evidence they present does not support their assertion regarding Australo-Melanesian mandibular morphology. One of two studies they cite has not been peer reviewed (the publication is just a conference abstract), whereas the other one has been severely criticized (4). Henneberg et al. also imply that a mandible from Roonka, Australia, supports their claim, but a CT scan of this specimen shows that it has a positive chin (Fig. 1). Thus, there is no reason to believe that living Australo-Melanesians often lack chins and therefore no reason to overturn Brown and Tomoko’s (3) assessment that the absence of chins in LB1 and LB6 precludes their attribution to H. sapiens.

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Fig. 1.

CT scans of the Liang Bua 1 mandible (Upper) and an Aboriginal Australian Homo sapiens mandible, Roonka 45 (Lower). The distinct internal buttressing of the symphysis that can be seen in LB1 is found in early hominins but not Homo sapiens. Both mandibles are to scale.

Henneberg et al. (1) and Eckhardt et al. (2) choose not to mention a number of other traits shared by the LB1 and LB6 mandibles that are also inconsistent with attribution to H. sapiens. Fig. 1 presents a CT scan of the LB1 mandible. It is obvious from this that, as has been pointed out previously (3), LB1 exhibits internal buttressing of the mandibular symphysis. This trait, which is also seen in LB6 (3), appears in earlier Homo but not H. sapiens. LB1 and LB6 also exhibit a strong extramolar sulcus, a trait found in early hominins but not H. sapiens (3). Additionally, LB1’s and LB6’s tooth root morphology differs from that seen in H. sapiens (3). DS cannot explain the presence of these traits in LB1 and LB6. Researchers who have studied modern people diagnosed with DS have not found these traits to be among the mandibular and dental features of DS (5, 6). Additionally, LB6 is accepted to be a normal individual by all researchers, including Eckhardt et al. (p. 11963 in ref. 2). Therefore, the only reasonable interpretation of the traits is that they are part of the normal biology of the population to which LB1 and LB6 belong. That LB1 and LB6 share the traits with early hominins but not H. sapiens refutes Henneberg et al.’s hypothesis.

Many interesting questions about the Liang Bua fossils remain unanswered, but whether LB1 is a pathological H. sapiens is not one of them. As we have demonstrated, the available mandibular evidence is already sufficient to discount this possibility.