The Laetoli Footprints September 15th , 1976

Not far from Olduvai George, a famous #fossil locality that was frequented by the Leakeys and colleagues, and a very important place where many lithic (stone) tools have been found, at first believed to be from Homo habilis, the first of our genus, but now is thought to be pushed back much farther in time to the Australopithecines.

Well, not far from here, on another excavation, Mary Leakey, wife of Louis Leakey, and discoverer of Zinj and many other important finds, hit the jackpot once again!

Amazingly, she came across a 75-ft trail of hominin footprints!!! It was unlike anything ever seen before!

So what does this mean? Well, as you can tell that is a two-legged, upright walking animal. This means they were , which only has occurred habitually in those of our clade, the Hominid family. This was proof, that our ancestors were walking upright at least 3.7 mya. This was the proof that so many had been looking for!

Many more footprints of hominins from Africa and Eurasia have been found since, but there was something special about these, and they’re still is today.

After later excavation by the #Leakeys and Dr. Tim White, it was concluded that the footprints must belong to #Australopithecus , or the species “Lucy” belongs to. Discovered in 1976, this would change our view of humanity forever.

Look at that!

What do you think about this?

Do a little research on the topic and lets start a discussion! What do you think the #ignificance of this find is to our understanding of #Human ?

Anatomy and Paleoanthropology, a chat with Dr. Bernard Wood

Premiering at Noon!

I am so excited to welcome you all to the next episode of ! On this episode, I am honored to talk to prestigious professor Dr. Bernard Wood of George Washington University. We discuss his career, starting as a surgeon and medical doctor and then finding his way into our deep human past and never looking back. Taking a unique look at our origins from an anatomical point of view, Dr. Wood has been a cornerstone of much of what we understand about hominin anatomy and evolutionary morphology.

“Bernard Wood is The University Professor of Human Origins and Professor of Human Evolutionary Anatomy at George Washington University. Dr. Wood is a medically qualified paleoanthropologist who practiced as a surgeon before moving into full-time academic life in 1972. In 1982, he was appointed to the S.A. Courtauld Chair of Anatomy in The University of London, and in 1985 he moved to The University of Liverpool to the Derby Chair of Anatomy and to the Chairmanship of the Department of Human Anatomy and Cell Biology. He was appointed the Dean of The University of Liverpool Medical School in 1995 and served as Dean until his move to Washington in the fall of 1997. When he was still a medical student, he joined Richard Leakey’s first expedition to what was then Lake Rudolf in 1968 and he has remained associated with that research group, and pursued research in paleoanthropology, ever since. His research centers on increasing our understanding of human evolutionary history by developing and improving the ways we analyze the hominin fossil record, and on using the principles of bioinformatics to improve the ways we store and collate data about the hominin fossil record. He has a special interest in the recognition of species and genera in the hominin fossil record, and he collaborates with researchers interested in the evolution of non-hominins in the interests of ensuring that we analyze hominin evolution in a proper comparative context. He has written one of the monographs in the series on the Koobi Fora site, and publishes papers on paleoanthropological topics. He is also the editor of the Wiley-Blackwell Encyclopedia of Human Evolution.”

If you learned something from this episode, or especially if you enjoyed it, be sure to like, subscribe, and share to support this Open Access, free Human Origins resource. The more we collectively know about our past, the more prepared we can be to create a bright future. Remember, there is always more to learn!

A new way of Analyzing Cave Art, Hominins in Europe, and Massive Hand Axes in Kent!

https://www.podbean.com/media/share/pb-t4596-148e348

Learn about: 

1.  How changing the way we look at rock art reveals so much more: https://phys.org/news/2023-08-topographical-elements-paleolithic-art-revealed.html
2. Hominins Evolved in Europe?: https://phys.org/news/2023-08-ancient-ape-trkiye-story-human.html
3. Massive 300,000-year-old Hand Axes Found in Kent: https://scitechdaily.com/scientists-discover-300000-year-old-giant-handaxe-in-rare-ice-age-site/

Understanding the ‘Muddle in the Middle’-Hominins from the Pleistocene-Guest Post by Mekhi

Introduction

Throughout the history of our evolution, few times  have confused  anthropologists more than the middle to late Pleistocene epoch. This time, from about 1 million years ago to 10,000 years ago, saw the emergence of our own species, along with our closest relatives, Neanderthals and the Denisovans. Sites from throughout Africa and into Europe give hints to our common ancestor with these other species, along with the origins of our own species, but perplexing morphologies in the fossil specimens make this time very confusing. Because of this, anthropologists have given this time the nickname, the ‘Muddle in the Middle’. 

From this time at the end of the Pleistocene, there are plenty of fossil hominins. Fossils have been found all throughout Africa, Europe, and even as far into Asia. It is not a lack of fossils that makes this period of time confusing, rather the morphologies seen within the fossils. Many fossils have very similar traits to one another, making it difficult to decipher what specimens belong to what species. To make it worse, the geography and locations of these fossils makes it more confusing. 

This time raises 3 main questions. First off, who was the common ancestor of us and our evolutionary cousins? Secondly, where did the Neanderthals even come from? And thirdly, and perhaps most important, where did we, Homo sapiens, come from? Though there is certainly no clear picture (at least, not yet), by examining all the fossils and evidence, we can get a decent understanding of what was happening in the infamous ‘Muddle in the Middle’. 

Who was our Common Ancestor?

There are several species which could possibly be the most recent common ancestor (MRCA) between us and Neanderthals (Homo neanderthalensis). The most commonly accepted species is Homo heidelbergensis, but there is little agreement on what fossils are and are not this species.

Homo heidelbergensis is a mid-late Pleistocene hominin which lived about 600,000-300,000 years ago. This species shared several traits with modern humans (Homo sapiens), but was also very different. This species had larger jaws, teeth and face, particularly in terms of their brow ridges and frontal sinus. Virtual reconstructions of what the MRCA should look like match the morphology seen in Homo heidelbergensis, giving more support to the idea that this species, or something like it, is the common ancestor. 

Fossils attributed to this species are found all throughout Africa and Europe. Specimens of Homo heidelbergensis from Africa, such as the Broken Hill skull (Kabwe 1) have been placed under the species name “Homo rhodesiensis”, though this taxa is not typically used. Other fossils from Europe may represent European H. heidelbergensis, but also might represent early, or ‘proto’ Neanderthals. One site in particular, in Spain, has provided many fossils from and can give great insight to understanding this mysterious time. 

The Kabwe 1 Homo heidelbergnsis cranial specimen from Zambia, southern Africa

Found in Atapuerca, Spain, the Sima de los Huesos (“pit of bones”) site possesses many fossil hominins attributed to Homo heidelbergensis and Homo neanderthalensis. This site contains 12 stratolithographic chambers, only one of which (LU-6), contains hominin remains, along with other animal remains, such as bears (Family: Ursidae). 

In this site, close to 8,000 fossil hominins have been found and excavated, making up roughly 30 individuals. Many of the specimens, such as the cranial specimen Atapuerca 5, have been attributed to Homo heidelbergensis, but resemble Neanderthals greatly in their morphology. This is seen especially in the dental remains from this site, of which there are over 30. 

These teeth give great insight to the origins of Neanderthals. If these teeth do indeed belong to Homo heidelbergensis, it may support the idea that this species was only ancestral to Neanderthals, and may represent an early Neanderthal lineage. 

Another species, also from Spain, may represent the common ancestor as well, Homo antecessor.

Homo antecessor is a species of late Pleistocene hominin which lived in Spain from 1.2 million-800,000 years ago. Found in Gran Dolina Cave, in Atapuerca, this species is the oldest known hominin from western and central Europe, giving clues to when humans first reached this area. This species lines up with the idea that humans migrated to Europe in several sporadic migrations/waves, with some of the oldest evidence of human habitation from Europe being stone tools dating to 1.2 million years ago. These tools suggest that humans adapted to the new European environments by improving their tools. 

Homo antecessor is sometimes considered to be early European Homo heidelbergensis, and was once considered to be the common ancestor of us and Neanderthals, but it is no longer typically thought to be that. Instead, this species is thought to be a sister species to H. heidelbergensis descending from Homo ergaster in Africa. 

The ATD6-15 and ATD6-69 specimens of Homo antecessor, making up the frontal and maxilla bones of the skull.

Throughout the years, many of the Pleistocene hominin fossils from across Europe and Africa and even into Asia have been given different species names, such as Homo capanensis, Homo mauritanicus, and Homo helmei. However, recently, a new species was suggested in an attempt to clear up the muddle in the middle. 

Homo bodoensis 

Named Homo bodoensis, this new species would have a geographical range of parts of Africa and Europe, possibly representing the MRCA. Homo bodoesnsis is composed of African specimens of Homo heidelbergensis along with some European specimens, while other European specimens which more closely resemble Neanderthals, such as the ones from Sima de los Huesos, were grouped in under Homo neanderthalensis, as early Neanderthals. 

Homo bodoensis is not widely accepted however, as many anthropologists believe that this could have been done but still under Homo heidelbergensis, saying that there is no need for an entirely new species. 

A chart showing the phylogenetic placements of Homo bodoensis and other hominin species

No matter what species name you use, the fossils clearly show the origins of Neanderthals and our shared common ancestor with them. However, it does little for the origins of our own species, Homo sapiens.

The Bodo cranium, associated with Homo heidelbergensis

Origins of Homo sapiens

The origins of our own lineage is one of the most interesting and important parts of this topic. Our species most likely arose out of Africa, though some have suggested we evolved in southwest Asia. Early fossils of Homo sapiens from Africa, though rare, show a lack of mosaic traits which is what would be expected in the LCA. Fossils such as Omo Kibish 1, Herto 1, and Herto 2, give further support to the idea that we arose in Africa, as they share a significant amount of derived traits with modern humans, and are likely some of the earliest known specimens of our own species. 

Fossils of early Homo sapiens have been found from all throughout Africa, such as Jebel Irhoud in Morocco, and Florisbad, in South Africa. The oldest fossil of our species, known as Jebel Irhoud, suggests that Homo sapiens most likely evolved around 300,000 years ago. 

The earliest Homo sapiens are referred to as ‘anatomically archaic’, and were morphologically different compared to anatomically modern Homo sapiens. They had larger brow ridges, a more extended skull, and overall looked more like earlier species such as Neanderthals. Archaic Homo sapiens existed from 300,000 to 160,000 years ago, when modern Homo sapiens took over. It wasn’t a sudden and quick transition however, as fossils show a chronological overlapping range in the variation of the two. 

The Jebel Irhoud cranium compared to a modern human

The Full Story

600,000 years ago in southern Africa, a new hominin species arose from Homo ergaster (African Homo erectus). This species, known as Homo heidelbergensis/Homo bodoensis, possessed many ancestral traits, such as a large extended skull, large teeth, large brow ridges, and a large frontal sinus, but also possessed with many derived traits, such as a more orthognathic face and a large frontal cortex. 

One population of this new species migrated out of Africa, where it encountered another species which also evolved from Homo ergaster, Homo antecessor, in Spain. Populations of this group out of Africa stayed in Europe, where they would give rise to Neanderthals, while other populations would move farther east, and would become our other cousins, the Denisovans. 

Homo heidelbergensis which remained in Africa would give rise to our own species, Homo sapiens. We would spread throughout Africa, then throughout the world, where we would encounter, interact with, breed with, and live with other human species, such as Neanderthals and Denisovans, until, by 40,000 years ago, we were the only ones left. 

Conclusion

The story of our evolution is one of the most extensively researched fields of science. The combination of fossil and genetic evidence gives a great understanding of our evolutionary past, but it isn’t always so clear. The mid-late Pleistocene is one such time. There are many hominin fossils from this time, but the confusing and mixed morphology makes it very difficult to identify and classify them into different species. Fossils from the Sima de los Huesos site in Spain are especially confusing. 

Many different species names have been proposed for certain fossils to clear things up, such as Homo heidelbergensis, Homo bodoensis, Homo capanensis, Homo mauritanicus, and Homo helmei, but there is little agreement on what species are valid or not, and this usually only confuses things more. Further research and discoveries, such as new fossils and genetic evidence are our best hope to resolve this confusing time. 

Sources

  1. Fran, Dorey. “Homo heidelbergensis”. The Australian Museum, 28-06-21, https://australian.museum/learn/science/human-evolution/homo-heidelbergensis/ 
  2. Godhino, M. R., Fitton, C. L., Toro-Ibacache, V., Stringer, B. C., Lacruz, S. R., Bromage, G. T., O’Higgins, P. (2018). The biting performance of Homo sapiens and Homo heidelbergensis. Journal of Human Evolution, 118, 56-71. https://doi.org/10.1016/j.jhevol.2018.02.010 
  3. Godhino, M. R., O’Higgins, P. (2017). The biomechanical significance of the frontal sinus in Kabwe 1 (Homo heidelbergensis). Journal of Human Evolution, 114, 141-153. https://doi.org/10.1016/j.jhevol.2017.10.007
  4. Stringer, C. (2012). The status of Homo heidelbergensis (Schoetensack 1908). Evolutionary Anthropology, 21(3), 101-107. https://doi.org/10.1002/evan.21311
  5. Perner, J., Esken, F. (2015). Evolution of human cooperation in Homo heidelbergensis: Teleology versus mentalism. Developmental Review, 38, 69-88. https://doi.org/10.1016/j.dr.2015.07.005
  6. “Kabwe 1”. The Smithsonian Institution’s Human Origins Program, 08-30-22. https://humanorigins.si.edu/evidence/human-fossils/fossils/kabwe-1 
  7. Mounier, A., Marchal, F., Condemi, S. (2009). Is Homo heidelbergensis a distinct species? New insight on the Mauer mandible. Journal of Human Evolution, 56(3), 219-246. https://doi.org/10.1016/j.jhevol.2008.12.006
  8. Czarnetzki, A., Jakob, T., Pusch, M. C. (2003). Paleopathological and variant conditions of the Homo heidelbergensis type specimen (Mauer, Germany). Journal of Human Evolution. 44(4), 479-495, https://doi.org/10.1016/S0047-2484(03)00029-0
  9. “Florisbad”. The Smithsonian Institution’s Human Origins Program, 08-30-22. https://humanorigins.si.edu/evidence/human-fossils/fossils/florisbad 
  10. Curnoe, D., Brink, J. (2010). Evidence of pathological conditions in the Florisbad cranium. Journal of Human Evolution, 59(5), 504-513. https://doi.org/10.1016/j.jhevol.2010.06.003
  11. Gracia-Téllez, A., Arsuaga, L, J., Martínez, I., Martín-Francés, L., Martinón-Torres, M., Bermúdez de Castro, M. J., Bonmatí, A., Lira, J. (2012). Orofacial pathology in Homo heidelbergensis: The case of Skull 5 from the Sima de los Huesos site (Atapuerca, Spain). Quaternary International, 295(8), 83-93. https://doi.org/10.1016/j.quaint.2012.02.005
  12. Sala, N., Pantoja-Pérez, A., Arsuaga, L. J., Pablos, A., Martínez, I. (2016). The Sima de los Huesos Crania: Analysis of the cranial breakage patterns. Journal of Archaeological Science, 72, 25-43. https://doi.org/10.1016/j.jas.2016.06.001
  13. Bermúdez de Castro, M. J., Martínez I., Gracia-Téllez, A., Martinón-Torres, M., Arsuaga, L. J. (2020). The Sima de los Huesos Middle Pleistocene hominin site (Burgos, Spain). Estimation of the Number of Individuals. The Anatomical Record, 304(7), 1463-1477. https://doi.org/10.1002/ar.24551
  14. Carretero, J., García-González, R.,  Rodríguez, L., Arsuaga, L. J. (2023). Main anatomical characteristics of the hominin fossil humeri from the Sima de los Huesos Middle Pleistocene site, Sierra de Atapuerca, Burgos, Spain: An update. The Anatomical Record.  https://doi.org/10.1002/ar.25194
  15. Martinón-Torres, M., Bermúdez de Castro, M. J., Gómez-Robles, A., Prado-Simón, L., Arsuaga, L. J. (2011). Morphological description and comparison of the dental remains from Atapeurca-Sima de los Huersos site (Spain). Journal of Human Evolution, 62(1), 7-58. https://doi.org/10.1016/j.jhevol.2011.08.007
  16. Martínez, I., Arsuaga, L. J., Quam, R., Carretero, M. J., Gracia, A., Rodríguez, L. (2007). Human hyoid bones from the middle Pleistocene site of the Sima de los Huesos (Sierra de Atapuerca, Spain). Journal of Human Evolution. 54(1), 118-124. https://doi.org/10.1016/j.jhevol.2007.07.006
  17. Dorey, Fran. “Homo antecessor”. The Australian Museum, 17-12-19, https://australian.museum/learn/science/human-evolution/homo-antecessor/
  18. Bermúdez de Castro, M. J., Martinón-Torres, M., Martín-Francés, L., Modesto-Mata, M., Martínez-de-Pinillos, M., García, C., Carbonell, E. (2017). Homo antecessor: The state of the art eighteen years later. Quaternary International, 433 (A)(17), 22-31. https://doi.org/10.1016/j.quaint.2015.03.049
  19. Barsky, D., Garcia, J., Martínez, K., Sala, R., Zaidner, Y., Carbonell, E, Toro-Moyano, I. (2013). Flake modification in European Early and Early-Middle Pleistocene stone tool assemblages. Quaternary International, 316(6), 140-154. https://doi.org/10.1016/j.quaint.2013.05.024
  20. Harvati, K., Reyes-Centeno, H. (2022). Evolution of Homo in the Middle and Late Pleistocene. Journal of Human Evolution, 173, 103279. https://doi.org/10.1016/j.jhevol.2022.103279
  21. Mallegni, F., Carnieri, E., Bisconti, M., Tartarelli, G., Ricci, S., Biddittu, I., Segre, A. (2003). Homo cepranensis sp. nov. and the evolution of African-European Middle Pleistocene hominids. Comptes Rendus Palevol. 2(2), 153-159. https://doi.org/10.1016/S1631-0683(03)00015-0
  22. Roksandic, M., Radović, P., Wu, X., Bae, J. C. (2022). Resolving the ‘Muddle in the Middle’: The case for Homo bodoensis sp. nov. Evolutionary Anthropology. 31(1), 20-29.  https://doi.org/10.1002/evan.21929
  23. “Bodo”. The Smithsonian Institution’s Human Origins Program. 08-30-22, https://humanorigins.si.edu/evidence/human-fossils/fossils/bodo
  24. Dorey, Fran. “Homo neanderthalensis-The Neanderthals”. The Australian Museum, 28-06-21. https://australian.museum/learn/science/human-evolution/homo-neanderthalensis/ 
  25. Stringer, C. (2016). The origin and evolution of Homo sapiens. Philosophical Transactions of the Royal Society B. 371(1698). https://doi.org/10.1098/rstb.2015.0237
  26. Bermúdez de Castro, M. J., Martinón-Torres, M. (2022). Quaternary International, 634(10), 1-13. https://doi.org/10.1016/j.quaint.2022.08.001 
  27. Dorey, Fran. “Homo sapiens-modern humans”. The Australian Museum, 16-10-20, https://australian.museum/learn/science/human-evolution/homo-sapiens-modern-humans/ 
  28. Callaway, E. (2017). Oldest Homo sapiens fossil claim rewrites our species’ history. Nature. https://doi.org/10.1038/nature.2017.22114
  29. Dorey, Fran. “The Denisovans”. The Australian Museum, 20-04-20, https://australian.museum/learn/science/human-evolution/the-denisovans/ 

Call for Papers

Cambridge Journal of Human Behaviour: Call for Submissions (Vol. 2, Issue 2)

The Cambridge Journal of Human Behaviour (CJHB) is now calling for submissions! CJHB is an internationally registered, peer-reviewed journal that is interdisciplinary in nature and dedicated to publishing the exceptional work of undergraduates from across the globe. 

We are a diamond open access journal, do not charge fees of any sort (subscription, processing, membership, or otherwise), and permit the author to re-publish their work elsewhere. 

The deadline for the second issue of Volume 2 is 22nd September, 2023. Submissions are always open and can be submitted online via our website: www.cjhumanbehaviour.com

 Specific details for submission:

  • Dissertations, projects, and extended essays welcome
  • 5,000 words maximum
  • Any topic relating to human behaviour (archaeology, anthropology, psychology, biology, etc.)
  • Interdisciplinary manuscripts strongly encouraged
  • All work must have been completed during the course of a student’s undergraduate studies
  • We are now also accepting book reviews
    • Word limit: 1,500
    • Reviews for books published in 2022 or later welcome 

More detail can be found on our website! For reference, check out our past issues here: https://cjhumanbehaviour.com/publications/

___________________

Any questions or concerns can be directed to myself Seth, at  cjhumanbehaviour.ba.outreach@gmail.com.

Cold Snap in Europe Brought an End to Ancient Humans, Inter-Glacial Passage in the Americas, and Genetics and Peptides in Neanderthals and Denisovans!

https://www.podbean.com/media/share/pb-5ewyh-1484822

On this week’s episode, we discuss the following topics:

1. https://www.sci.news/othersciences/anthropology/paleoanthropology/early-pleistocene-extreme-glacial-cooling-12170.html
2. https://www.sci.news/medicine/neanderthal-denisovan-antimicrobial-peptides-12187.html
3. https://www.sci.news/medicine/neanderthal-denisovan-antimicrobial-peptides-12187.htm

What does AI think of the Naledi finds and their Effects on Popular Culture and Science Communication?

What are the controversies surrounding the new homo naledi finds? What do they mean for the field of paleoanthropology and science communication in general? How do we move forward?

Homo naledi is a fascinating and mysterious species of ancient humans that was discovered in 2013 in the Rising Star cave system near Johannesburg, South Africa. The fossils, which belong to at least 15 individuals, have a mix of primitive and modern features, such as a small brain, curved fingers, and a human-like foot. The researchers who found them, led by palaeoanthropologist Lee Berger, have claimed that H. naledi is a new species that lived between 335,000 and 241,000 years ago, and that it deliberately buried its dead in deep chambers of the cave.

However, these claims have been met with sharp criticism and controversy from other experts in the field, who have questioned the validity of the new species designation, the evidence for intentional burial, and the dating of the fossils. Some have also accused Berger of rushing his findings to the public without proper peer review, and of creating a media circus that undermines the credibility of palaeontology.

In this blog post, I will examine some of the main points of contention and debate surrounding the new H. naledi finds, and discuss what they imply for the study of human evolution and the dissemination of scientific knowledge.

Is H. naledi a new species or not?

One of the most fundamental questions about H. naledi is whether it represents a distinct species or not. Berger and his colleagues have argued that H. naledi is different enough from other known hominins (the group that includes humans and their extinct relatives) to warrant a new species name. They have pointed out that H. naledi has a unique combination of traits that are not found in any other hominin, such as its small brain size (about 500 cubic centimeters), its slender body shape, its long legs relative to its arms, and its flared pelvis.

However, some critics have challenged this view, and have suggested that H. naledi is actually a variant of an already known species, such as Homo erectus or Homo heidelbergensis. They have argued that H. naledi’s traits are not so unique or unusual, and that they fall within the range of variation seen in other hominins. They have also pointed out that H. naledi’s skull shape and teeth are very similar to those of H. erectus, and that its small brain size could be explained by environmental factors or genetic drift.

The debate over H. naledi’s species status is not likely to be resolved anytime soon, as it depends on how one defines a species and how one interprets morphological data. There is no clear-cut criterion for determining what constitutes a species in palaeontology, and different methods can yield different results. Moreover, fossil evidence is often incomplete and fragmentary, making it difficult to compare different specimens and populations.

Did H. naledi bury its dead or not?

Another controversial issue about H. naledi is whether it intentionally buried its dead or not. Berger and his colleagues have proposed that H. naledi deliberately disposed of its deceased members in deep chambers of the Rising Star cave system, which they accessed through narrow passages that required climbing and crawling skills. They have based this hypothesis on several lines of evidence, such as:

– The absence of any signs of predation or scavenging on the bones

– The lack of any other animal remains or artifacts in the chambers

– The differences between the soil composition inside and outside the chambers

– The presence of articulated bones (bones that are still connected in their original position)

– The occurrence of etched symbols on some cave walls near the chambers

However, these lines of evidence have been contested by other researchers, who have offered alternative explanations for how the bones ended up in the chambers. Some have suggested that H. naledi’s bodies were washed into the chambers by water or mud flows, or that they fell into natural traps or pits. Some have also suggested that H. naledi’s bones were disturbed by later human activity or geological processes, or that they were artificially selected by Berger’s team based on their location.

The debate over H. naledi’s burial behavior is also unlikely to be settled soon, as it depends on how one interprets taphonomic data (the study of how fossils are formed and preserved). There are many factors that can affect the preservation and distribution of fossils in caves, such as water flow, sedimentation, erosion, bioturbation (the movement of animals or plants), human interference, etc. These factors can create complex and variable scenarios that are hard to reconstruct with certainty.

How old are H. naledi’s fossils?

A third contentious issue about H. naledi is how old its fossils are. Berger and his colleagues have estimated that H. naledi lived between 335,000 and 241,000 years ago, based on a combination of methods, such as uranium-thorium dating, electron spin resonance dating, and palaeomagnetic dating. They have argued that this age range is consistent with H. naledi’s morphology and phylogeny (its evolutionary relationship to other hominins).

However, some critics have questioned the accuracy and reliability of these methods, and have suggested that H. naledi’s fossils are much older or much younger than the estimated age range. Some have argued that the methods used by Berger’s team are prone to errors or contamination, or that they do not reflect the true age of the fossils, but rather the age of the sediments or minerals that surround them. Some have also argued that H. naledi’s morphology and phylogeny do not match its proposed age range, and that it should be either more primitive or more derived than it appears.

The debate over H. naledi’s age is also difficult to resolve, as it depends on how one applies and evaluates different dating techniques. There is no single method that can provide a definitive answer to the age of a fossil, and different methods can have different assumptions, limitations, and uncertainties. Moreover, dating results can be affected by various factors, such as sample quality, calibration, contamination, etc. These factors can introduce errors or discrepancies that need to be accounted for and explained.

What do these controversies mean for palaeoanthropology and science communication?

The controversies surrounding the new H. naledi finds have important implications for the field of palaeoanthropology and the communication of scientific knowledge in general. On one hand, they reflect the challenges and uncertainties that are inherent in studying human origins and evolution, which rely on limited and often ambiguous fossil evidence. On the other hand, they also reflect the diversity and dynamism of scientific inquiry and debate, which involve different perspectives, methods, and interpretations.

The controversies also highlight the need for transparency and openness in conducting and reporting scientific research, especially in a field that has a high public interest and impact. Berger and his colleagues have been praised for their innovative and collaborative approach to studying and sharing H. naledi’s fossils, which involved:

– Recruiting a large and diverse team of young researchers from around the world

– Publishing their results in an open-access journal with peer review comments

– Providing 3D files of their fossils for anyone to download and print

– Inviting feedback and criticism from other experts and the public

However, Berger and his colleagues have also been criticized for their sensationalist and premature presentation of their findings, which involved:

– Announcing their discoveries in press conferences and documentaries before peer review

– Making bold claims without sufficient evidence or consensus

– Ignoring or dismissing alternative hypotheses or interpretations

– Creating hype and confusion among the media and the public

The controversies thus raise questions about how to balance between speed and accuracy, between accessibility and quality, between outreach and rigor in scientific research and communication.

How do we move forward?

The controversies surrounding the new H. naledi finds are not likely to be resolved in the near future, as they require more data, analysis, and discussion. However, they also offer opportunities for advancing our understanding of human evolution and improving our practice of science communication.

To move forward, we need to:

– Collect more fossils of H. naledi from different sites and regions

– Apply more methods of dating, morphometrics (the measurement of shapes), genetics (the study of DNA), etc.

– Compare H. naledi with other hominins from different time periods and locations

– Test different hypotheses about H. naledi’s behavior, ecology (the study of interactions with the environment), culture (the study of learned behaviors), etc.

– Engage in constructive dialogue and debate with other researchers

– Publish our results in reputable journals with rigorous peer review

– Share our data and methods with other researchers and the public

– Communicate our findings in clear and accurate ways

– Acknowledge our uncertainties and limitations

– Invite feedback and criticism from other experts and the public

By doing these things, we can hope to gain a better picture of who H. naledi was, what it did, how it lived, when it died, and how it relates to us.

New Human Lineages and Ancient Burials

https://www.podbean.com/media/share/pb-7bupp-147b169

Join Paleoanthropologist and Rock Art researcher Genevieve von Petzinger and Founder and Science Communicator Anthropologist Seth Chagi as they tackle some of the week’s most interesting topics, taking a deep dive and explaining to you why these stories make our headlines! 

How is Cave Art Preserved? Cave Art 101

Get ready for this Saturday’s episode of the Q&A edition of #CaveArt101! 

Genevieve, once again, is here to answer your questions about Ice Age Rock Art! For this episode, Muhammed asked, “How do weather conditions and climate changes affect the formation and preservation of artworks in the Ice Age? Were there any specific techniques used to preserve these artworks in the face of climate change and the harsh living conditions during that period?”

Be sure to watch this episode to catch the answer, and catch all the previous episodes to learn all about Cave and Rock Art! 

Do you want to get your question answered? Please submit it to worldofpaleoanthropology@gmai.com