3.3-Million-Year-Old Baby Shows Lucy's Species Hung Out in Trees

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The advent of upright walking was a really big deal in human evolution. Scientists have posited that it allowed our ancestors to see above the savanna grass (the better to spot predators and prey), to carry tools and food and babies, to travel long distances more efficiently and to better strut their stuff for potential mates, among other possible perks. Indeed, bipedalism is one of the defining characteristics of our kind. Understandably, then, paleanthropologists are kind of obsessed with how our quadrupedal predecessors made the shift to two feet. Now a new study adds to the growing body of evidence that the transition did not happen overnight.

The 1974 discovery of Lucy, the 3.2-million-year old skeleton of an ancestral species known as Australopithecus afarensis, demonstrated that our ancestors evolved adaptations to upright walking before brain size expanded (another key human trait). But experts disagreed vehemently over just how dedicated Lucy’s species was to life on the ground. Some thought that A. afarensis had thoroughly abandoned the trees, that its anatomy demanded a terrestrial lifestyle and that any features suggestive of tree climbing were merely harmless evolutionary holdovers from an arboreal ancestor. Others maintained that A. afarensis still spent a considerable amount of time in the trees, and that the arboreal traits figured importantly in the survival of the species.

Eventually the idea that A. afarensis was a committed biped seemed to eclipse the competing theory. Then in 2006 researchers led by Zeresenay Alemseged, now at the California Academy of Sciences, announced their discovery of an astonishingly complete skeleton of an A. afarensis youngster, dubbed Selam, who died at the age of three. They unearthed the specimen at a site in the Afar region of Ethiopia called Dikika, just a few kilometers from the site of Hadar, where Lucy was found. Importantly, the 3.3-million-year-old skeleton preserves complete shoulder blades, which contain clues to locomotion. In their initial report describing Selam, Alemseged and his colleagues hinted that her shoulder blade anatomy resembled that of a gorilla, suggesting that early human ancestors spent more time climbing trees than previously supposed. The more detailed analysis by Alemseged and David Green of Midwestern University, published in the October 26 Science, confirms that preliminary assessment.


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Green and Alemseged compared Selam’s shoulder blades to those of adult and juvenile great apes, as well as other fossil humans. They found that hominoids (the group composed of apes and humans, living and extinct) have two kinds of shoulder blade: one in which the socket faces up and another in which the socket faces sideways. Modern Homo sapiens and fossil members of our genus have the latter type of shoulder blade. Selam, however, has the upward facing kind. She also has another apelike shoulder trait in that the ridge of bone that cuts across the blade, known as the scapular spine, is oriented obliquely rather than horizontally as it is in modern humans. This upward orientation of the shoulder socket and the oblique orientation of the scapular spine help living apes to climb in trees.

Whereas modern human shoulder blades morph during development from a more apelike form into the human form, ape shoulder blade shape remains stable—and probably australopithecine shoulder blade shape did too, according to the new study. Thus the apelike appearance of Selam’s shoulder should not be dismissed as merely a juvenile trait. Instead, Green and Alemseged conclude, the findings bolster the hypothesis that A. afarensis “participated in a behavioral strategy that incorporated a considerable amount of arboreal behaviors in addition to bipedal locomotion.”

In a commentary accompanying the new report, Susan Larson of Stony Brook University notes that the famous Homo erectus (sometimes called H. ergaster) skeleton known as the Turkana Boy shows that the shoulder of human ancestors underwent its transformation by around 1.8 million years ago. “This reconfiguration was likely part of the emergence of our own genus Homo,” she observes, “and a growing dependence on tools and culture for survival.”

 

Kate Wong is an award-winning science writer and senior editor for features at Scientific American, where she has focused on evolution, ecology, anthropology, archaeology, paleontology and animal behavior. She is fascinated by human origins, which she has covered for nearly 30 years. Recently she has become obsessed with birds. Her reporting has taken her to caves in France and Croatia that Neandertals once called home to the shores of Kenya’s Lake Turkana in search of the oldest stone tools in the world, as well as to Madagascar on an expedition to unearth ancient mammals and dinosaurs, the icy waters of Antarctica, where humpback whales feast on krill, and a “Big Day” race around the state of Connecticut to find as many bird species as possible in 24 hours. Wong is co-author, with Donald Johanson, of Lucy’s Legacy: The Quest for Human Origins. She holds a bachelor of science degree in biological anthropology and zoology from the University of Michigan. Follow her on Bluesky @katewong.bsky.social

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