I'll be making a tabulation of Neandertal specimens that have yielded molecular (DNA, proteomic) sequence information. I know there are more than 30 but I'd like to get an actual count and link photos where possible. This will take a while, and I'll add to this thread as I go.
The first mtDNA fragments published from any Neandertal specimen were from the humerus of the Neandertal 1 skeleton, from the Kleine Feldhofer Grotte near Mettmann, Germany. The partial skeleton was recovered in 1856. Sequencing by Matthias Krings et al. doi.org/10.1016/S0092-…
Ralf Schmitz and Jürgen Thissen relocated sediments from the Kleine Feldhofer Grotte, excavating in 1997 and 2000. They found new bone fragments that refit the Neandertal 1 skeleton and a humerus fragment (NN 1) that must represent a second individual. doi.org/10.1073/pnas.1…
Schmitz et al. 2002 reported the partial mtDNA sequence of the NN 1 humerus fragment, distinct from the Neandertal 1 mtDNA sequence. They examined another fragment, NN 4, which did not yield DNA. Pictured here is NN 1 with refitted fragments NN 2, NN 3 and NN 47.
The third and fourth Neandertals on my list are together a strange case. In 2000, Michael Scholz and coworkers reported that they carried out DNA-DNA hybridization from bone extracts from fossil material, including two "Neandertals". doi.org/10.1086/302949
Other specialists in ancient DNA analysis immediately challenged these results, arguing that basic standards had not been met and results were probably driven by contamination, not endogenous Neandertal DNA. No sequence information was generated. doi.org/10.1086/316948
The first specimen sampled in this study was a parietal bone from Warendorf-Neuwarendorf, Germany. This was attributed to Neandertals by Scholz et al. 1999 and Czarnetzki and Trellisó-Carreño 1999. Little has been published on this specimen.
The second is a clavicle that Scholz et al claimed was from Krapina. They provided this information (and no photo): "Krapina Fe. 1.si/213 Geological and Paleontological Museum, Zagreb, Croatia". There were two weird things about this...
First, the curator of the museum in Zagreb at the time couldn't substantiate that this bone was actually from Krapina. The paper cited no permits, no permissions. The bone seemed to come out of nowhere.
Second, the number provided, "Krapina Fe.1.si/213" corresponds to a femur fragment, not a clavicle, and it's still in Zagreb. This wouldn't be the last time that a DNA paper on Neandertals had some really fishy provenence, but it may be the most egregious.
Was this actually a Neandertal? With a site that was dug 100 years before this paper, there was a chance that bone had been distributed to Tübingen early in the 20th century and remained in that collection. But I still don't know.
The second partial mtDNA sequence from a Neandertal to be published was from the rib of an infant skeleton from Mezmaiskaya Cave, Russia. Work done by Ovchinnikov et al. 2000 doi.org/10.1038/350066…
The infant skeleton was the first individual to be uncovered at the site, described by Golovanova et al. 1999. Later this specimen would be numbered as Mezmaiskaya 1. doi.org/10.1086/515805
Mezmaiskaya 1 was the target of additional sequencing in several later studies, including the Briggs et al. sequencing of the complete mtDNA doi.org/10.1126/scienc… and partial nuclear genome recovery by Green et al. 2010. doi.org/10.1126/scienc…
Before I leave Mezmaiskaya 1, let me share this wonderful reconstruction of the skeleton done by Marcia Ponce de Leon and coworkers in 2008. doi.org/10.1073/pnas.0…
Mezmaiskaya 2 is a second individual, unearthed later from a different, more recent, context at the site. It is reported to include 24 cranial fragments. Briggs et al. 2009 recovered a partial mtDNA sequence from this specimen doi.org/10.1126/scienc…
I haven't been able to find a scientific description or photos of Mezmaiskaya 2. It has been mentioned in the context of dating at the site, including a direct C14 AMS date (uncalibrated 39,700 ± 1,100 14C BP) reported in 2011 by Pinhasi et al. doi.org/10.1073/pnas.1…
Next on the list of Neandertals with DNA successes is a specimen from Vindija, Croatia. Vindija is maybe the most important of the Neandertal sites for ancient biomolecules, ranking with Denisova. Most samples come from the G3 layer, between 45 and 50,000 years old.
Krings et al. 2000 doi.org/10.1038/79855 reported a partial mtDNA sequence from Vi-75, one of the G3 Vindija specimens. This is a fragment that Malez and Ullrich 1982 identified as a metatarsal fragment. I cannot find a photo of this third Neandertal to yield DNA data.
A word about photos: Many Neandertal fragments that have generated DNA were targeted for biomolecular investigation because they preserve little anatomical information. Before digital photography and online journal publications, it was rare to publish photos of such fragments.
This practice has changed somewhat in recent years as photography and preparation of photos for publication has become much cheaper and easier. But published catalogs of fossil sites with photos of all specimens are still rare. Archival photos are more common but hard to access.
Krings et al. 2000 reported extracting bone powder and assessing amino acid racemization on 15 Neandertal specimens from Vindija layer G3. From 7 that appeared to have good biomolecular preservation, they selected Vi-75 as the most promising for further investigation.
Small fragments of mtDNA from two additional Vindija fossils were reported by Serre et al. 2004. In that paper, the two fossils were numbered Vi-77 and Vi-80. These numbers, and Vi-75, once inspired some confusion. doi.org/10.1371/journa…
Ahern et al. 2004 provided some useful background on the excavation and numbering system at Vindija. Malez excavated in the 1970s and 1980s. A new numbering system was put into place during the late 1990s. doi.org/10.1016/j.jhev…
Old specimen numbers of the Vi-75, Vi-77 kind were catchalls for area designations. Nondiagnostic hominin bone fragments that may originally have been placed with bulk faunal material started with these numbers. Once identified, they were given numbers in the new system.
Vi-77 was not part of later DNA work, and I haven't found the full Vindija catalog that would tell its new number. Vi-80 was renumbered as Vi 33.16. This fragment of tibia is one of the most important fossil hominins ever discovered.
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Quite like the new paper by my @UWMadison colleague @apragsdale. Fun to see lots of people newly discovering these ideas about metapopulation models! A couple of notes: nature.com/articles/s4158…
An implication of this population model is that the structure of our species, Homo sapiens, began to emerge several hundred thousand years earlier than the dispersal that led to Neandertal and Denisovan populations.
When added to other evidence of recurring gene flow between Neandertal and African ancestral populations, this very strongly implies that Neandertals are Homo sapiens.
So this seems very unpopular for some reason, but humans DID evolve from apes. We did not evolve from chimpanzees, gorillas, or any other living apes. They are our cousins. Our close fossil relatives were like living great apes in many ways and more like humans in others.
Today's great apes, including chimpanzees and bonobos, two species of gorillas, and three species of orangutans, are a small surviving remnant of the diversity of apes that once existed. Each evolved in ways that helped them survive, just as our ancestors did.
Paleontologists have discovered many more forms of extinct apes than living ones. They were adapted to their time and place, some Asian, some African, and some European, but did not survive to the present day. Many of them lived in the period before 5 million years ago.
Some discussion in comments last week in @ScienceMagazine about "paleodemes" with a short defense of the value of the concept. I think the paleodeme concept has most of the problems of paleo species concepts with none of their benefits. science.org/doi/10.1126/sc…
The person probably most responsible for the paleodeme concept in human origins is Clark Howell, whose 1999 paper "Paleo-Demes, Species Clades, and Extinctions in the Pleistocene Hominin Record" defined (although it did not first introduce) the concept. journals.uchicago.edu/doi/abs/10.108…
As presented by Howell, a paleodeme corresponds to a regional sample of fossils across a delimited range of time, with some morphological distinctiveness. These were groups like "Neandertal", "Skhūl/Qafzeh", or "Petralona/Atapuerca-Sima".
Interesting paper on cutmark evidence from Olduvai, further substantiating early access to animal carcasses by tool-wielding Early Pleistocene hominins. @SciReportsnature.com/articles/s4159…
The paper's discussion raises lots of reasons why the anatomy of early Homo supports the idea that they were competent hunters. On this I don't disagree, but I think that focusing on "early Homo" here is misleading for several reasons.
First, "early Homo" fossils overlap substantially in anatomy with Australopithecus and Paranthropus. So much that we cannot always tell them apart (including long-standing arguments about well-known and not-so-fragmentary fossils).
So, Homo longi. It's such a good name. Dragon people. And an amazing skull discovery. Adds to our knowledge of the Middle Pleistocene in China. But it's sad that the name is not going to stay. cell.com/the-innovation…
The boring reason why we can't use the Homo longi name is technical. The research puts the Harbin skull together with the Dali skull, and Xinzhi Wu gave that the name Homo sapiens daliensis more than 40 years ago. So IF there's a species, it has to be H. daliensis.
In case you wonder how close Harbin looks to Dali, here is Harbin on the left and Dali (which has some crushing to the maxilla) on the right. As Weidenreich might have said, they resemble each other as closely as one egg resembles another.
The new report of fossil material from Nesher Ramla, Israel, claims a "previously unknown archaic Homo population" some 140,000 years ago. It's a big claim in an area where most scientists have thought that early modern humans and Neandertals interacted. science.sciencemag.org/content/372/65…
Looking at the morphology of the mandible NR-2, it falls within the variation of fossils attributed to Neandertals, and is similar to Krapina, which is around the same age, and Sima, which are early Neandertals. This seems like a basic early Neandertal jaw.
The other fossil NR-1 is a complete right parietal bone and fragments of the left parietal. The analysis of shape places is near late Neandertals and early Neandertals, but a bit less "barrel-shaped", thereby similar to generalized H. erectus and African Middle Pleistocene Homo.