Pluridisciplinary evidence for burial for the La Ferrassie 8 Neandertal child


The origin of funerary practices has important implications for the emergence of so-called modern cognitive capacities and behaviour. We provide new multidisciplinary information on the archaeological context of the La Ferrassie 8 Neandertal skeleton (grand abri of La Ferrassie, Dordogne, France), including geochronological data -14C and OSL-, ZooMS and ancient DNA data, geological and stratigraphic information from the surrounding context, complete taphonomic study of the skeleton and associated remains, spatial information from the 1968–1973 excavations, and new (2014) fieldwork data. Our results show that a pit was dug in a sterile sediment layer and the corpse of a two-year-old child was laid there. A hominin bone from this context, identified through Zooarchaeology by Mass Spectrometry (ZooMS) and associated with Neandertal based on its mitochondrial DNA, yielded a direct 14C age of 41.7–40.8 ka cal BP (95%), younger than the 14C dates of the overlying archaeopaleontological layers and the OSL age of the surrounding sediment. This age makes the bone one of the most recent directly dated Neandertals. It is consistent with the age range for the Châtelperronian in the site and in this region and represents the third association of Neandertal taxa to Initial Upper Palaeolithic lithic technocomplex in Western Europe. A detailed multidisciplinary approach, as presented here, is essential to advance understanding of Neandertal behavior, including funerary practices.


Elaborate funerary activity is unique to the human lineage1 and the emergence of this behavior can be framed within the broader context of the increasing complexity of cognitive and symbolic capacities. While it has been suggested that the Middle Pleistocene human bone accumulation at Sima de los Huesos could have had an anthropic origin2,3,4, relatively complete articulated hominin skeletons are extremely rare in the paleontological record prior to MIS 5, then are known Homo sapiens remains at Skhul and Qafzeh5,6,7 and Neandertals from Shanidar8 and possibly Tabun1,9,10. High diversity in Neandertal mortuary practices has been proposed on the basis that chronologically and geographically close groups engaged in varying behaviors, ranging from cannibalism to intentional burial of some of their dead11. However, the question of whether or not Neandertals buried their dead has been continually debated since the discovery of the La Chapelle-aux-Saints 1 Neandertal12,13,14,15,16,17,18,19,20. Another question has been whether the proposed burials constitute evidence of symbolic behaviour per se19. These discussions parallel the historical debate concerning the physical appearance and abilities of Neandertals, from the brute represented originally by M. Boule21 to the opposite tendency22. The topic of Neandertal burial is highly controversial, raising questions about the similarity in funerary activity between the two highly encephalized human species, the question of cultural transmission between the two groups and the underlying intention behind the practice (symbolism vs utilitarism). Additionally, criteria for burial recognition have been discussed but remain disputable because some of the criteria proposed as a threshold to prove the presence of Middle Paleolithic burials would not allow some historical burials to be classified as such12,13,14,15,16,17,18,19,20,23,24,25,26. Thus, the Neandertal burial debate can sometimes reach beyond the scientific framework to an ideological level. This scientific literature, whether for or against the recognition of Neandertal burials, has limitations that render their conclusions debatable and debated12,13,14,15,16,17,18,19,20. Moreover, the application of the disputed criteria to individual archaeological cases is problematic. La Ferrassie is one of the key sites in this debate due to the extensive and well-preserved fossil record, including several Neandertal partial and complete skeletons.

The grand abri (large rock-shelter) de la Ferrassie site (Savignac de Miremont, Dordogne, France; Supplementary Fig. S1) and Shanidar (Iraqi Kurdistan) are the two Middle Paleolithic sites that have yielded the largest collections of partial to complete Neandertal skeletons, interpreted as intentional burials8,27,28,29,30,31,32,33. La Ferrassie has yielded seven partial or complete Neandertal skeletons: two adults (possibly a male and a female) and five partial skeletons of children of different ages-at-death (Supplementary Fig. S2)34,35,36,37. Most of these skeletons were found at the beginning of the twentieth century38,39,40,41,42,43. The last skeleton, La Ferrassie 8 (LF8), a partial Neandertal skeleton (cranium, neck and trunk bones, pelvis and four hand phalanges) of a child of around two-years-old, was found in 1970 and 1973 in layer M2, during the penultimate excavation of the site between 1968 and 197328,30,31,43. Only a few non-human skeletal remains and lithics are associated with the skeleton. The discovery and context of this skeleton has generally been regarded as poorly documented30,36,43,44, but in fact this deficiency stems from a lack of the necessary processing of the information and materials from La Ferrassie related to the penultimate excavation phase (1968–1973). Indeed, a huge amount of data remained unassessed prior to our current study. The in-depth processing and examination of the material and the insights gained are crucial as other potential instances of Neandertal burial in Europe, including La Chapelle-aux-Saints 1 and the other La Ferrassie specimens, were discovered more than a century ago when data recording of stratigraphy and context was well below modern archaeological standards.

Here we present new data on the LF8 child context from three sources (Supplementary Texts S1-S2). First, the careful reading of the field diaries (housed at the Musée d'Archéologie nationale et Domaine national de Saint-Germain-en-Laye, noted MAN hereafter) and the processing of the spatial data recorded during the excavations at the site performed between 1968 and 1973. Second, we performed multidisciplinary studies on the LF8 skeleton and associated archaeo-paleontological findings. The results include new data on the excavation in 1970 and 1973 of the LF8 Neandertal child, the stratigraphic context and spatial information of the LF8 findings, the first geochronological analysis of the LF8 individual (using 14C and OSL dates), Zooarchaeology by Mass Spectrometry (ZooMS) data of the associated unidentified skeletal remains, ancient DNA analysis, and a complete taphonomic analysis of the collection of available human and faunal remains. Third, new excavations and analyses were performed in 2014 at the La Ferrassie site in the location where LF8 was found. In this framework, our objective here is to discuss whether the evidence from LF8 is compatible with an anthropogenic deposition of the corpse and to provide the most parsimonious scenario to explain the origin of the preservation and representation of the LF8 bones. The results from this individual can provide upstream information for the Neandertal burial debate.


LF8 Neandertal child: spatial and stratigraphic context

The MAN archives provided data to contextualize and precisely locate the area where LF8 was found within the La Ferrassie Grand abri, and its position relative to the other Neandertal skeletons (Fig. 1 and Supplementary Fig. S2). LF8 was found in square 1, at the western extent of the 1968–1973 excavations, in the layer named M2 in this area during the excavations. In 1970, a 50 cm wide trench was dug perpendicular to the wall of the rockshelter to get insights into the stratigraphy in this area. This area corresponds to the eastern half of square 1 (Supplementary Text S2). This trench revealed layers K and L (Aurignacian), a “lower Perigordian” layer (i.e., Châtelperronian, named L2bj) and a sedimentary layer (considered basically sterile at that time) that contained seven teeth and two parietal fragments belonging to LF8, which were recognized during the sieving of the sediment. The archaeological level within the thick sedimentary layer was later named M2 in 1973 when the rest of the human remains were found. In 1973, during the final excavation days (August 24th–30th), elements labelled from number 295 (the first human bone identified) up to 538 were collected. More recently, forty-seven human remains, including cranial remains, mandibular fragments, vertebral and costal remains and two hand phalanges were identified among the indeterminate paleontological remains, mainly from the 1970, but also 1973 field seasons31, which add significantly to the completeness of the skeleton. The attribution of these remains to LF8 was based on their consistency with the existing remains in terms of size and age-at-death, the lack of anatomical duplication, the direct refitting of bone elements, and their spatial location within the La Ferrassie stratigraphy31. The field notebooks provide detailed information on the spatial distribution of the 1968–1973 findings (Supplementary data 1), including the density of the findings from layer M2, and their general spatial organization and orientation, relative to the other layers. The LF8 remains were found associated with faunal remains and lithics. It should be noted that there is no clear difference in terms of technology, state of preservation, or type of lithics between the two limited samples of lithic elements coming from the layers M2 and L2Bj in square 1 but sample size is small for both assemblages, rendering comparisons difficult.

Figure 1

(A) Zenithal view of the 3D model of the LF8 excavation area after the 2014 field season, with (B) the different excavations performed in the area: the easternmost part (x = 50–100) was excavated in 1970 (green), the westernmost part in 1973 (red) and the area shown in the black square in 2014. This latter area includes a column of approximately 20 × 60 × 80 cm in the westernmost area and the surface of the southern part of the area excavated in 1973. The location of the schematic representation of the LF8 remains is shown. (C) Schematic representation of the LF8 remains (modified from43 and original documentation), including the position of the different anatomical parts, in which we have added the horncore remains (in red) based on the available spatial information. (D) Left: Northern profile of the LF8 area after the 2014 excavation (the numbers of the photos indicate a stratigraphic division in which the uppermost layer would be equivalent to the L2B-L2Bj complex from Delporte). Center: The depth where the OSL samples were taken in this profile. Right: W–E scatterplot (XZ) of the 1970–1973 findings. Note the west–east downwards inclination of the elements found in layers L2B, L2Bj and M1, the reverse east–west downward inclination of the elements found in layer M2, and the absence of archaeo-paleontological findings between the elements found in layer M2 and those of the overlying layers, as well as the sterile basal part of M2 in the eastwards direction (highlighted in grey). The archaeo-paleontological findings (found in the layer that contained the child in 1970—green dots—and 1973—red dots) extend for c. 120 cm in the E–W orientation, c. 50 cm in the N–S orientation and a regular vertical extension of c. 25 cm, taking into account that the finds, when plotted as a group, show an inclination of 15º to the west. Here we also show the location of the Neandertal tooth fragment (LF13) discovered in 2014 in the dirt layer of the previous excavations. The yellow dots correspond to the samples used for the radiocarbon chronology and the blue dots correspond to the OSL samples. We also summarize here the radiocarbon ages in cal BP (95.4%) and OSL dates (see Table 1 for the detail and Supplementary data, Fig. S10 for a more complete visualization of the position of the dated samples).

The information about the geological and stratigraphic context of LF8 deriving from the excavations in 1968–1973 is very limited. The place where LF8 was found was an area of low sediment deposition compared to the westernmost part of the site45. Moreover, a general north-east inclination of the archaeological layers is observed in this sector as illustrated by the stratigraphic sketches made during these excavations46. In addition, a similar pattern is visible when we plot the findings of Delporte’s excavations for all the layers, including the L2B-L2Bj complex, located just above the layer M2 (Supplementary Fig. S6 and S10). The level M2, where LF8 was found, is archaeo-paleontologically sterile except in the limited area where this individual was found. This was noted by Delporte in his diaries for squares 1 and 2 and we have been able to confirm it (Supplementary Text S2). The features of the loose sediment associated with the LF8 remains are consistent with that found at the site close to the location where LF8 was found (Supplementary Text S2).

Interestingly, the LF8 remains and associated archaeo-paleontological findings show a relatively strong inclination to the west, in contrast to the general dip of M2 or other strata in this sector (Fig. 1), which indicates that they do not follow the natural dip of the stratum that contains it. The LF8 head remains were found to the East while the pelvic elements were found to the West and at a greater depth (Fig. 1). The LF8 remains are scattered in the west–east axis over an area of 94 cm, while the dispersion of the LF8 elements in the north–south direction is low (~ 20 cm), and just one hand phalanx was found 10 cm to the south. Finally, the cranial parts are topographically higher than the pelvis (~ 30 cm).

2014 excavations

In August 2014, we went back to the field in order to gain additional insights in the LF8 sector. We were able to confirm a great density in archaeological findings at the same depth as Delporte’s L2B-L2Bj complex, in adjacent squares (Supplementary Fig. S10). Moreover, in the area where we excavated, i.e., 50 cm to the west of square 1, the geological layer at the same depth where LF8 was discovered was basically sterile. It was also possible to directly confirm that the area where LF8 was found had been completely excavated. As a result, the new field season did not provide additional information on the LF8 context but confirmed previous observations: the general inclination of the layers above LF8, and the discrepancy between the reconstructed inclination of the LF8 assemblage within M2 (based on the spatial information recorded by Delporte) relative to the sedimentary layer that contains it and to the contact with the L2Bj layer.

We found a new Neandertal fossil, a molar fragment of an individual older than 5 years, at the beginning of our excavation, within the dirt layer on the surface of Square 1, deeper than the archaeological assemblage associated with LF8 (Supplementary SI text 2, Fig. S13). This was the only archaeological finding on the entire excavation surface (100 cm × 50 cm) of the LF8 area in the approximatively 10 cm depth that we excavated. We hypothesize that this element likely fell from one of the surrounding profiles just before the excavation of the 1973 field season ended. The anatomical features observed on this fragment are consistent with a Neandertal lower left molar (Supplementary Text S2). Following our other recent human fossil discoveries in the La Ferrassie collections 47, we name this specimen LF13.

Geochronological context

In order to obtain a chronological framework for the stratigraphic sequence preserved in the LF8 sector, four sediment samples were collected for luminescence dating in the stratigraphic section exposed to the north of square 1 during the 2014 excavations (Fig. 1). The first of these dating samples was taken from the rich archaeological level corresponding to Delporte’s levels L2B and L2Bj, yielding a result of 43 ± 6 ka using the minimum dose model (MDM48) or 54 ± 3 using the Internal External Uncertainty model (IEU49) (Supplementary Text S2 and Table S1). The MDM results are consistent with five 14C dates of bone samples from the same layer excavated in both 2014 (between 49.1–43.3 and 44.2–42.5 ka cal BP, 95.4%) and 1970 (44.6–43.3 ka cal BP 95%) (Table 1; Supplementary Table S1). The other three (deeper) OSL dates yielded older results. The sample at the same depth where LF8 was found yielded an age of 60 ± 7 ka (MDM) or 66 ± 4 ka (IEU) (Supplementary Table S6). Ten faunal remains from Delporte’s excavations associated with LF8 yielded 14C dates ranging between 45.5–39.5 ka cal BP (95.4%) (Table 1). In fact, the dates associated with the LF8 child are either of similar age or younger than those from the overlying level, the L2B-L2Bj complex (Fig. 1; Supplementary Fig. S10). Finally, in addition to the ten faunal remains associated with LF8, one element classified as a hominin through ZooMS yielded an age of 41.7–40.8 ka cal BP (95.4%). Mitochondrial DNA of this directly dated hominin groups with Neandertals (Supplementary Table S5).

Table 1 AMS radiocarbon dating of 17 samples from La Ferrassie.

Zooarchaeology by mass spectrometry (ZooMS)

Most (n = 13) of the 17 taxonomically unidentified bone specimens associated with the LF8 skeleton analysed by ZooMS were identified as Bos/Bison, which is consistent with the taxonomical assessment of the macro-faunal remains associated to LF8 (Supplementary Table S8). From the remaining four, two could not be identified taxonomically, one belonged to an ursid (Ursus sp.), and one was a hominin specimen. Additionally, 14 bone remains from the layer overlying the LF8 deposit (L2Bj) were analysed to provide a comparative context for the deamidation data of the specimens associated with LF8. The deamidation data of the bones associated to the LF8 remains are similar to those from L2Bj, except for the ursid specimen that shows a different signature (Supplementary Fig. S15). This ursid specimen also yielded a radiocarbon age of 39.0–38.6 ka cal BP (95.4%), the youngest of the radiocarbon ages on bone material associated to the LF8 child. Both the younger chronology and the different deamidation value suggest a different post-depositional history than the other ZooMS-analysed samples from this area. As a result, this bear specimen indicates that the bones spatially associated with LF8 contain material that is either from different chronological and/or diagenetic histories. However, this ursid specimen is the exception, as the rest of the analysed material shows similarity in deamidation data, as well as great homogeneity in taphonomic indicators and 14C dates. The presence of this specimen might therefore reasonably be explained by an excavation or sampling error in 1970 (Supplementary, Text, Figs. S5, S9, S12).

Taphonomy of the LF8 skeleton and associated remains

A taxonomical and taphonomic study was performed on a total of 4609 paleontological remains, including the 191 elements belonging to the LF8 child. This exhaustive analysis includes all the recovered skeletal material associated with this important discovery. Most (NR = 3,492) were indeterminate, small (< 25 mm), burnt bone fragments. Only 22 of the 127 anatomically identifiable faunal remains were taxonomically identifiable and corresponded to cranial remains and diaphyseal remains of Bos/Bison (NR = 9), Equus ferus (NR = 7) and cervids (NR = 6), including some fetal remains (Supplementary Tables S8, S9, S10). The taphonomic and taxonomic spectrum of the faunal sample is entirely consistent with the results from the new excavations carried out at La Ferrassie. Among the faunal remains associated with LF8, the largest corresponds to a bison (Bison sp.) horncore that was found in situ in 1973 in more than 25 fragments that were found close to each other.

The taphonomic results (Supplementary Text S1) point towards the presence of two different groups: the human remains and the faunal remains. The human pieces are complete (or almost), were recovered in close spatial association (for some anatomical regions, possibly anatomically connected), and represent a single individual. Animal remains consist of scattered fragments belonging to various individuals that show carnivore marks, cut-marks, green-bone fractures and fire alterations. None of these alterations have been observed on the human remains. Conversely, taphonomic alterations specific to the burial conditions are similar for both samples. Thus, these data highlight two different biostratinomic (i.e., prior-to-burial) scenarios, but similar burial conditions (same sedimentary context).


The La Ferrassie 8 Neandertal child constitutes the last of the Neandertal skeletons found at the La Ferrassie rock-shelter (in 1970 and 1973). The published contextual data for this individual has been limited to a drawing of the scattering of the bones published in monographs28,36,43. The analysis of the contextual data together with the finding of new remains31, the taxonomic and taphonomic analysis of the whole collection, and a robust chronological context provide the tools for the interpretation of the archaeo-paleontological context of this child for the first time. After the evaluation of the data, we propose what we consider the most parsimonious scenario to explain this specific case.

The LF8 child shows a W-E orientation, with the head (to the E) located at a higher elevation than the pelvic bones (to the W). This inclination does not follow the natural dip of the level where this child was found (M2) or of the overlying archaeological layers (the L2B-L2Bj complex). The faunal remains associated with LF8 directly dated with 14C are either of the same age or younger than the 14C results for the bones found in the overlying layer. The 14C dates obtained in samples from the L2B-L2Bj complex are similar to the OSL date obtained at the same elevation. In contrast, the 14C dates of the remains associated with LF8 are younger than the OSL date of the geological layer at the same depth where LF8 was found. Finally, the 14C age of one hominin bone fragment identified by ZooMS and genetically linked to Neandertal using mitochondrial DNA is among the youngest ages of all the analysed elements. The most parsimonious explanation is that this hominin bone also belongs to LF8. The obtained age (ETH-99102: 36,170 ± 220 14C BP) is consistent with the most recent chronology for the Châtelperronian at La Ferrassie 50 and is the same age as the directly dated Neandertal remains from Saint-Césaire (OxA-18099: 36,200 ± 750 14C BP) and Arcy-sur-Cure (MAMS-25149: 36,840 ± 660 14C BP), which have been associated with the same techno-complex51,52 (but see53). Moreover, these three dates, together with those from Goyet11, constitute the most recent directly dated Neandertal remains. This observation does not engage us in the current debate concerning the Châtelperronian artisan. We need additional data and new sites to definitively assess the role of Neandertals in the development of this techno-complex and the possible influence of the first Homo sapiens. In fact, the recent finding of the oldest Homo sapiens with jewellery in central Europe54 has fueled the debate regarding the possible acculturation of Neandertals, which is beyond the scope of the current study.

Regarding the human remains, the absence of carnivore marks, the low degree of spatial disturbance, fragmentation, and weathering suggest that they were rapidly covered by sediment. The LF8 remains are very well preserved, despite belonging to a child which are generally more delicate. Additionally, there are clear differences in the preservation of the human remains, on the one hand, and the associated faunal remains on the other. These two groups have different post-mortem and taphonomic histories. It also should be noted that based on both Delporte’s reports and our own excavations the M2 layer, where LF8 was found, is sterile except in the zone where LF8 was found (Fig. 1).

Should the corpse have been laid on the floor (whether intentionally or otherwise), in the absence of erosive processes a similar inclination of the human remains and the rest of the strata would be expected. Moreover, we could expect a wider spread of the archaeological remains. Currently, we cannot find any natural (i.e. non-anthropic) process that could explain the presence of the child and associated elements within a sterile layer with an inclination that does not follow the geological inclination of the stratum. In this case, we propose that the body of the LF8 child was laid in a pit dug into the sterile sediment. The similarity of the sediment filling this hypothetical pit to the surrounding sediments, together with post-depositional processes present at the site28,55, made it impossible to ascertain the limits of the pit during the excavation process56. However, the spatial distribution of the objects associated with LF8 inside the sterile sediment offers an archaeological clue to the presence and extent of the pit (Fig. 1).

The proposed scenario is consistent with the limited surface in which archaeo-paleontological remains were found within the M2 layer (essentially, only LF8 and the associated remains). This scenario would also explain the apparent stratigraphic problems with the chronology, i.e., the 14C dates of the elements associated with the LF8 individual are either similar in age or younger than the dates from the layers overlying the LF8 individual. In addition, the directly dated hominin fragment has yielded one of the youngest 14C dates of the dated assemblage. Moreover, it would also explain the apparent discrepancy between the OSL and 14C dates in the M2 level, which indicates that the paleontological elements are younger than the time of deposition of the sediment that surrounds them. This discrepancy is not seen in the L2B-L2Bj layer complex overlying the LF8 skeleton, where the OSL ages (minimum dose mode) agree with the 14C dates. Agreement between the OSL ages and 14C dates was also observed in other sectors of the La Ferrassie site, demonstrating consistency between the two methods for determining the chronology of the site (level 6, Châtelperronian50). The

deamidation data of the bones from L2Bj are very similar to those of the hominin specimen and the fauna remains associated with LF8, indicating similar diagenetic conditions, with the exception of just one specimen (Supplementary Text S2; Fig. S15). Moreover, the bones from L2Bj have similar 14C dates to the Neandertal specimen and the fauna remains associated with LF8. There is no clear difference in terms of technology, state of preservation and constitution between the two limited collections of lithics coming from layers M2 and L2B-L2Bj in square 1.

However, the LF8 remains extend for c. 120 cm, which is longer than would be expected for the head and trunk of a two-year old Neandertal child. Based on the spatial information, there is a high degree of anatomical consistency in the distribution of the LF8 remains. However, the poor photographic documentation of the 1973 excavation and the rapid excavation progression mean that we cannot ascertain whether some anatomical elements of the LF8 child were found in similar anatomical positions observed for other Neandertal children, such as Amud 7 or Dederiyeh 114,56,57. It is interesting to note that the Neandertal record comprises several well preserved immature individuals whose state of preservation, taphonomic condition and geochronological situation within their respective sites is unique compared to other hominin species.

There are some difficulties in the interpretation of LF8 that need to be discussed. The anatomical representation of LF8 is restricted to the cranium, thorax, pelvis, and four hand phalanges31. The reason for the lack of upper and lower limbs (excepting hand phalanges) remains unsolved. It should be noted that only the adult Neandertal skeletons from La Ferrassie are complete. All five immature skeletons are partial34,35,36, which could result from different reasons (differential burial, taphonomic processes, differential care in the excavation process). The recent excavations of the LF8 sector did not reveal the missing anatomical parts of LF8. Neither did the analysis of the museum collections31, although these did provide a better representation of the anatomical regions already known. We propose several possibilities to explain this paradox. Firstly, the child was complete at burial, and the subsequent disappearance was the result of geological post-depositional processes and/or the excavation conditions and/or museum curation conditions. Indeed, the southern and western borders of the area where LF8 was found were possibly exposed during the Capitan and Peyrony excavations. As a result, the missing bones could have been lost at any moment between the 1920’s and 1968. Alternatively, the anatomical distribution of LF8 could be the result of secondary purposeful burial, or a partial primary burial27. In any case, geological processes are likely (at least partially) responsible for the more scattered distribution of the human remains in the W–E direction. Based on the available evidence, these should be regarded as alternative explanatory hypotheses, as we cannot firmly conclude on this topic. However, the absence of upper and lower limbs, which are more robust, if not fragmented, than postcranial axial skeletal elements (e.g., vertebrae) which in this case are excellently preserved given their fragility, does not affect the other scientific evidence described in this study.

The new information about the LF8 individual can be compared to the other individuals from La Ferrassie in order to see whether they follow the same pattern. First, the E–W orientation of the LF8 skeleton is also observed for both adult individuals. In both adult cases, the head is also topographically higher than the pelvis. These two skeletons were located with a separation of around 50 cm between their heads, with LF2 being located more westward than LF1. Additionally, D. Peyrony, H. Breuil and M. Boule observed small packets of yellow sand mixed with the Mousterian sediments associated with both adult individuals58. These packets were not observed elsewhere in the Mousterian layers, but correspond to sediment from the underlying layers. This observation has been interpreted as the effect of intentional funerary pits that removed sediment from the underlying level and mixed it with the sediment filling the pit58. The presence of a triangular-shaped pit covered with a triangular-shaped stone was also proposed for the partial LF6 infant59. A recent taphonomic analysis of the LF1 adult individual indicates that the fracture pattern and the absence of surface modification on this skeleton, together with its overall completeness is also consistent with an intentional burial, as proposed by previous studies32. Future complementary approaches should compare our multidisciplinary information with similar data from other sites that yielded Neandertal immature individuals, such as Dederiyeh or Amud.

Additional studies of the other specimens from La Ferrassie should aim to provide the same level of detail now available for LF8 and LF131,32. This multidisciplinary approach should also be extended to other Neandertal skeletons and sites, to provide robust data that will allow us to contextualize information at both the site and regional scale. This is necessary to seriously address historically debated issues such as the relationship of Neandertals with the Châtelperronian industry and the chronological and geographical extent of funerary behaviours60, as well as providing a more precise chronology for the last Neandertals.


The combined anthropological, spatial, geochronological, taphonomic and biomolecular data analysed here suggest that a burial is the most parsimonious explanation for LF8. Our results show that LF8 is intrusive within an older (and archaeologically sterile) sedimentary layer. We propose that Neandertals intentionally dug a pit in sterile sediments in which the LF8 child was laid. The skeleton was laid in an E (head)–W (pelvis) orientation (as are all the Neandertal skeletons found in the site for which we have information), with the head higher than the rest of the skeleton (as can be deduced for LF1 and LF2 from the information in Boule’s archive at the IPH). Some lithics and faunal remains that were on the ground at the time of burial could have fallen into the pit while it was being prepared or filled. The sterile sediment removed previously would have been used to fill the pit and cover the child. This would explain why the faunal remains associated with LF8 have a similar (or younger, in the case of the directly dated hominin fragment) 14C age compared to the faunal remains found in the overlying layer. These dates are also in agreement with the OSL age of the overlying layer, whereas the OSL age of level M2 at the elevation of LF8 is much older. The direct date obtained on a Neandertal bone fragment, identified by ZooMS and confirmed through ancient DNA, is the first direct date from a human from La Ferrassie, yielding an age contemporaneous to the directly dated Neandertals from Saint-Césaire in Poitou–Charentes and Arcy-sur-Cure Grotte du Renne in Burgundy France. These new results provide important insights for the discussion about the chronology of the disappearance of the Neandertals, and the behavioural capacity, including cultural and symbolic expression, of these humans.

Material and methods

A complete re-inventory of the anthropological collections of the Muséum national d’Histoire naturelle has been facilitated by their transfer to the Jardin des Plantes from the Musée de l’Homme (Paris, France) due to renovations. Several boxes contained elements from the site of La Ferrassie (Dordogne, France) where new human fragments were identified. Some elements fit with the LF1 and LF2 skeletons. Another box contained elements from the excavations of Delporte in 1973 that were related to the discovery of LF8. To complement the information available in this box, including the new human remains, we visited the collections and archives of the excavations led by Delporte in La Ferrassie from 1968 to 1973 at the Musée d'Archéologie nationale et Domaine national de Saint-Germain-en-Laye (noted MAN). This provided a better understanding of the context of the 1968–1973 excavations and their results (Supplementary Text S1). Graphic documentation, including photographs of square 1 from the final days of the 1973 field season were useful to visualize and understand the process of the excavations. Notebooks with information about the labelling and 3D coordinates of each element were crucial to reconstruct the spatial distribution of the Mousterian layer and the LF8 elements (Supplementary Text S2, supplementary data 1 for the raw data used, and Figs. S6 and S10). The notebooks for square 1 (field seasons 1970, 1972 and 1973) are entirely reproduced (SI Supplementary data 1). Among the boxes in the MNHN and in the MAN, several fragments of a partial bison horncore that perfectly refit together were discovered (Supplementary Text S2) as well as numerous new human remains of LF8 (Supplementary Text S2). The attribution of the new human remains to LF8 is based on their consistency with the existing remains in terms of size and age-at-death, the lack of anatomical duplication, the direct refitting of bone elements, their location in the deposit, and the taphonomic analyses (following the methodology of Rendu and colleagues16) of the entire fossil bone collection, including the horn and other faunal elements and the complete hominin collections. The archives of Marcelin Boule (housed at the MNHN and at the Institut de Paléontologie Humaine, Paris, France) were visited in order to search for information regarding the La Ferrassie site. In order to provide a more thorough evaluation of the original LF8 context, we present new data on the archaeo-stratigraphic context of the LF8 Neandertal child including: spatial data of the LF8 fossils and associated finds, taphonomic analysis of LF8 and the associated faunal remains, stratigraphic information regarding the findings from the LF8 sector (both from Delporte’s excavation and our own excavation in 2014), new luminescence and 14C ages and ZooMS data of some indeterminate fossil remains associated to LF8. The methodologies follow classic protocols and are detailed elsewhere (Supplementary Text S1). The methods used for the retrieval and analysis of ancient mitochondrial DNA are described in detail in Supplementary Text S1.


  1. 1.

    Pettitt, P. B. The Neanderthal dead: Exploring mortuary variability in Middle Palaeolithic Eurasia. Before Farm. 1, 1–19 (2002).

    Google Scholar 

  2. 2.

    Arsuaga, J. L. et al. Neandertal roots: Cranial and chronological evidence from Sima de los Huesos. Science 344, 1358–1363 (2014).

    ADS  CAS  PubMed  Article  PubMed Central  Google Scholar 

  3. 3.

    Arsuaga, J. L. et al. Postcranial morphology of the middle Pleistocene humans from Sima de los Huesos, Spain. Proc. Natl. Acad. Sci. U.S.A. 112, 11524–11529 (2015).

    ADS  CAS  PubMed  PubMed Central  Article  Google Scholar 

  4. 4.

    Sala, N. et al. Lethal interpersonal violence in the Middle Pleistocene. PLoS ONE 10(5), e0126589 (2015).

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  5. 5.

    Valladas, H. et al. Thermoluminiscence dating of Mousterian “Proto-Cro-Magnon” remains from Israel and the origin of modern man. Nature 331, 614–616 (1988).

    ADS  Article  Google Scholar 

  6. 6.

    Schwarcz, H. P. et al. ESR dates for the hominid burial site of Qafzeh in Israel. J. Hum. Evol. 17, 733–737 (1988).

    Article  Google Scholar 

  7. 7.

    Stringer, C. B., Grün, R., Schwarcz, H. P. & Goldberg, P. ESR dates for the hominid burial site of Es Skhul in Israel. Nature 338, 756–758 (1989).

    ADS  CAS  PubMed  Article  PubMed Central  Google Scholar 

  8. 8.

    Pomeroy, E. et al. New Neanderthal remains associated with the ‘flower burial’ at Shanidar Cave. Antiquity 94, 11–26 (2020).

    Article  Google Scholar 

  9. 9.

    Grün, R., Stringer, C. B. & Schwarcz, H. P. ESR dating of teeth from Garrod’s Tabun cave collection. J. Hum. Evol. 20, 231–248 (1991).

    Article  Google Scholar 

  10. 10.

    Grün, R. & Stringer, C. B. Tabun revisited: revised ESR chronology and new ESR and U-series analyses of dental material from Tabun C1. J. Hum. Evol. 39, 601–612 (2000).

    PubMed  Article  PubMed Central  Google Scholar 

  11. 11.

    Rougier, H. et al. Neandertal cannibalism and Neandertal bones used as tools in Northern Europe. Sci. Rep. 6, 29005 (2016).

    ADS  CAS  PubMed  PubMed Central  Article  Google Scholar 

  12. 12.

    Gargett, R. H. Grave shortcomings: The evidence for Neanderthal burial. Curr. Anthropol. 30, 157–190 (1989).

    Article  Google Scholar 

  13. 13.

    Gargett, R. H. Middle Palaeolithic burial is not a dead issue: The view from Qafzeh, Saint-Césaire, Kebara, Amud, and Dederiyeh. J. Hum. Evol. 37, 27–90 (1999).

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  14. 14.

    Rak, Y., Kimbel, W. H. & Hovers, E. A Neandertal infant from Amud Cave, Israel. J. Hum. Evol. 26, 313–324 (1994).

    Article  Google Scholar 

  15. 15.

    Sandgathe, D. M., Dibble, H. L., Goldberg, P. & McPherron, S. P. The Roc de Marsal Neandertal child: A reassessment of its status as a deliberate burial. J. Hum. Evol. 61, 243–253 (2011).

    PubMed  Article  PubMed Central  Google Scholar 

  16. 16.

    Rendu, W. et al. Evidence supporting an intentional Neandertal burial at La Chapelle-aux-Saints. Proc. Natl. Acad. Sci. U.S.A. 111, 81–86 (2014).

    ADS  CAS  PubMed  Article  PubMed Central  Google Scholar 

  17. 17.

    Dibble, H. L., Aldeias, V., McPherron, S. P., Sandgathe, D. M. & Steele, T. E. A critical look at evidence from La Chapelle-aux-Saints supporting an intentional Neandertal burial. J. Archaeol. Sci. 53, 649–657 (2015).

    Article  Google Scholar 

  18. 18.

    Rendu, W. et al. Let the dead speak… comments on Dibble et al.’s reply to “Evidences supporting an intentional burial at La Chapelle-aux-Saints”. J. Archaeol. Sci. 69, 12–20 (2016).

    Article  Google Scholar 

  19. 19.

    Chase, P. G. & Dibble, H. L. Middle Paleolithic symbolism: A review of current evidence and interpretations. J. Anthrop. Archeol. 6, 263–296 (1987).

    Article  Google Scholar 

  20. 20.

    Pettitt, P.B. The Paleolithic Origins of Human Burial (Routledge, 2011).

  21. 21.

    Boule, M. L'homme fossile de la Chapelle-aux-Saints. Ann. Paléontol. 6, 111–172; 7, 21–56, 85–192; 8, 1–70 (1911–1913).

  22. 22.

    Coon, C.S. The Races of Europe (Macmillan, 1939).

  23. 23.

    Belfer-Cohen, A. & Hovers, E. In the eye of the beholder: Mousterian and Natufian burials in the Levant. Curr. Anthropol. 33, 463–471 (1992).

    Article  Google Scholar 

  24. 24.

    Hovers, E., Belfer-Cohen, A. Insights into early mortuary practices of Homo, in The Oxford Handbook of the Archaeology of Death and Burial (S. Tarlow, L. Nilsson-Stutz, Eds.) 631–642 (Oxford University Press, 2013).

  25. 25.

    Pettitt, P. Hominin evolutionary thanatology from the mortuary to funerary realm: The palaeoanthropological bridge between chemistry and culture. Philos. Trans. R. Soc. B Biol. Sci. 373 (2018).

  26. 26.

    Stutz, A.J., Nilsson Stutz, L. Burial and ritual in The International Encyclopedia of Biological Anthropology (W. Trevatah, Ed.) (Springer, 2018).

  27. 27.

    E. Trinkaus, The Shanidar Neandertals (Academic Press, 1983).

  28. 28.

    Delporte, H. Le Grand Abri de la Ferrassie (Éditions du Laboratoire de Paléontologie Humaine et de Préhistoire, 1984).

  29. 29.

    Cowgill, L. W., Trinkaus, E. & Zeder, M. A. Shanidar 10: A Middle Paleolithic immature distal lower limb from Shanidar Cave, Iraqi Kurdistan. J. Hum. Evol. 53, 213–223 (2007).

    PubMed  Article  PubMed Central  Google Scholar 

  30. 30.

    Laville, D. La Ferrassie: Taphonomie d'un Site Sépulcral Moustérien. in Master thesis, Université de Liège (2007).

  31. 31.

    Gómez-Olivencia, A., Crevecoeur, I. & Balzeau, A. La Ferrassie 8 Neandertal child reloaded: New remains and re-assessment of the original collection. J. Hum. Evol. 82, 107–126 (2015).

    PubMed  Article  PubMed Central  Google Scholar 

  32. 32.

    Gómez-Olivencia, A. et al. La Ferrassie 1: New perspectives on a “classic” Neandertal. J. Hum. Evol. 117, 13–32 (2018).

    PubMed  Article  PubMed Central  Google Scholar 

  33. 33.

    Pomeroy, E., Mirazón Lahr, M., Crivellaro, F., Farr, L. et al. Newly discovered Neanderthal remains from Shanidar Cave, Iraqi Kurdistan, and their attribution to Shanidar 5. J. Hum. Evol. 111, 102–118 (2017).

  34. 34.

    Heim, J. L. Les Hommes fossiles de la Ferrassie I. Le gisement Les squelettes adultes (crâne et squelette du tronc) (Masson, Paris, 1976).

    Google Scholar 

  35. 35.

    Heim, J.L. Les Hommes Fossiles de La Ferrassie. II. Les Squelettes d'Adultes: Squelettes des Membres (Masson, Paris, 1982).

  36. 36.

    Heim, J. L. Les enfants néandertaliens de la Ferrassie. Étude anthropologique et analyse ontogénique des hommes de Néandertal (Masson, Paris, 1982).

    Google Scholar 

  37. 37.

    Maureille, B. A lost Neanderthal neonate found. Nature 419, 33–34 (2002).

    ADS  CAS  PubMed  Article  PubMed Central  Google Scholar 

  38. 38.

    Capitan, L. & Peyrony, D. Deux squelettes humains au milieu de foyers de l’epoque moustérienne. La Revue l’Ecol. d’Anthropol. Paris 4, 402–409 (1909).

    Google Scholar 

  39. 39.

    Capitan, L. & Peyrony, D. Un nouveau squelette humain fossile. Revue Anthropol. 1, 148–150 (1911).

    Google Scholar 

  40. 40.

    Capitan, L. & Peyrony, D. Trois nouveaux squelettes humains fossiles. C. R. Séances l’Acad. Inscriptions Belles-Lettres 56, 449–454 (1912).

    Article  Google Scholar 

  41. 41.

    Capitan, L., Peyrony, D. in 44e Session de l'Association Française Pour l'Avancement des Sciences (Association Française Pour l'Avancement des Sciences, 1920).

  42. 42.

    Breuil, H. Communication sur les squelettes de La Ferrassie. L’Anthropologie 31, 342–344 (1921).

    Google Scholar 

  43. 43.

    Heim, J.L. Les squelettes moustériens de la Ferrassie. in Le Grand Abri de la Ferrassie (H. Delporte, Ed.) 249–271 (Éditions du Laboratoire de Paléontologie Humaine et de Préhistoire, Paris, 1984).

  44. 44.

    Maureille, B., Laville, D., Mennecier, P. in Première Humanité. Gestes Funéraires des Néandertaliens (B. Vandermeersch, J.-J. Cleyet-Merle, J. Jaubert, B. Maureille, A. Turq, Eds.) 97–106 (Réunion des Musées Nationaux, Paris, 2008).

  45. 45.

    Texier, J.P. Histoire Géologique de Site Préhistoriques Classiques du Périgord: Une Vision Actualisée (Cths, 2009).

  46. 46.

    Laville, H., Tuffreau, A. in Le Grand Abri de la Ferrassie (H. Delporte, Ed.) 25–50 (Éditions du Laboratoire de Paléontologie Humaine et de Préhistoire, Paris, 1984).

  47. 47.

    Becam, G. et al. Isolated teeth from La Ferrassie: Reassessment of the old collections, new remains, and their implications. Am. J. Phys. Anthropol. 169(1), 132–142 (2019).

    PubMed  Article  PubMed Central  Google Scholar 

  48. 48.

    Galbraith, R. F., Roberts, R. G., Laslett, G. M., Yoshida, H. & Olley, J. M. Optical dating of single and multiple grains of quartz from Jinmium rock shelter, northern Australia: Part I, experimental design and statistical models. Archaeometry 41, 339–364 (1999).

    Article  Google Scholar 

  49. 49.

    Thomsen, K. J., Murray, A. S., Bøtter-Jensen, L. & Kinahan, J. Determination of burial dose in incompletely bleached fluvial samples using single grains of quartz. Radiat. Meas. 42, 370–379 (2007).

    CAS  Article  Google Scholar 

  50. 50.

    Guérin, G. et al. A multi-method luminescence dating of the Paleolithic sequence of La Ferrassie based on new excavations adjacent to the La Ferrassie 1 and 2 skeletons. J. Archaeol. Sci. 58, 147–166 (2015).

    Article  Google Scholar 

  51. 51.

    Hublin, J. J. et al. Radiocarbon dates from the Grotte du Renne and Saint-Césaire support a Neandertal origin for the Châtelperronian. Proc. Natl. Acad. Sci. U.S.A. 109(46), 18743–18748 (2012).

    ADS  CAS  PubMed  PubMed Central  Article  Google Scholar 

  52. 52.

    Welker, F. et al. Palaeoproteomic evidence identifies archaic hominins associated with the Châtelperronian at the Grotte du Renne. Proc. Natl. Acad. Sci. U.S.A. 113(40), 11162–11167 (2016).

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  53. 53.

    Gravina, B. et al. No reliable evidence for a Neanderthal-Châtelperronian association at La Roche-à-Pierrot, Saint-Césaire. Sci. Rep. 8, 15134 (2018).

    ADS  PubMed  PubMed Central  Article  CAS  Google Scholar 

  54. 54.

    Hublin, J. J. et al. Initial Upper Palaeolithic Homo sapiens from Bacho Kiro Cave, Bulgaria. Nature 581, 299–302 (2020).

    ADS  CAS  PubMed  Article  PubMed Central  Google Scholar 

  55. 55.

    Bertran, P., Caner, L., Langohr, R., Lemée, L. & d’Errico, F. Continental palaeoenvironments during MIS 2 and 3 in southwestern France: the La Ferrassie rockshelter record. Quat. Sci. Rev. 27, 2048–2063 (2008).

    ADS  Article  Google Scholar 

  56. 56.

    Hovers, E., Kimbel, W. H. & Rak, Y. The Amud 7 skeleton—Still a burial. Response to Gargett. J. Hum. Evol. 39, 253–260 (2000).

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  57. 57.

    Akazawa, T., Muhesen, T. Neanderthal Burials. Excavations of the Dederiyeh Cave, Afrin, Syria (KW Publications Ltd., Auckland, 2003).

  58. 58.

    Maureille, B., Van Peer, P. Une donnée peu connue sur la sépulture du premier adulte de La Ferrassie (Savignac-de-Miremont, Dordogne)/A little known element concerning the burial of the first adult at La Ferrassie (Savignac-de-Miremont, Dordogne) Paléo 10, 291–301 (1998).

  59. 59.

    Peyrony, D. Les moustériens inhumaient-ils leurs morts. Bull. Soc. Hist. Archéol. Périgord 58, 132–139 (1921).

    Google Scholar 

  60. 60.

    Pomeroy, E. et al. Issues of theory and method in the analysis of Paleolithic mortuary behavior: A view from Shanidar Cave. Evol. Anthrop. 2020, 1–17 (2020).

    Google Scholar 

  61. 61.

    Bronk Ramsey, C. & Lee, S. Recent and planned developments of the program OxCal. Radiocarbon 55, 720–730 (2013).

    Article  Google Scholar 

  62. 62.

    Reimer, P. et al. The IntCal20 northern hemisphere radiocarbon age calibration curve (0–55 cal kBP). Radiocarbon 62, 725–757 (2020).

    CAS  Article  Google Scholar 

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AGO was funded by a Marie Curie-IEF (FP7-PEOPLE-2012-IEF 327243) research fellowship during part of this work, currently is funded by a Ramón y Cajal fellowship (RYC-2017-22558) and has also received support from the Spanish FEDER/Ministerio de Ciencia e Innovación-Agencia Estatal de Investigación (project PGC2018-093925-B-C33), Research Group IT1418-19 from the Eusko Jaurlaritza-Gobierno Vasco. We thank A. Fort, A. Froment, D. Grimaud-Hervé, V. Laborde, P. Mennecier, L. Huet (direction des collections, MNHN) for providing access to the collections of the MNHN and help during our study of that material. We thank A. Schmidt, E. Essel, D. López-Herráez, J. Kelso, S. Nagel, S. Pääbo, J. Richter, B. Schellbach and A. Weihmann for help with the DNA analysis and sequencing and their support of the project. M. Balasse (UMR 7209, CNRS-MNHN), L. Chiotti, F. Détroit, M. Lebon, L. Puymerail (UMR 7194, CNRS-MNHN), and P. Wils (UMS 2700, CNRS-MNHN) provided helpful comments and discussions. E. Pomeroy corrected the English and provided helpful comments on a previous version of this work. E. Hovers and J. Rios-Garaizar also provided helpful comments on a previous version of this manuscript. J. Rios-Garaizar provided help with a map. V. Aldeias, S. McPherron, D. Sandgathe and P. Goldberg provided stimulating and helpful discussions all along this research, on the field and while analyzing the data. H. Dibble has also greatly contributed to this project, we missed the last discussion. F. Goussard (UMR 7207, CNRS-MNHN), L. Bruxelles (UMR 5608), S. Madelaine (MNP) and D. Geffard-Kuriyama (UMS 2700, CNRS-MNHN) assisted the illustrations. M. García-Sanz (UMS 2700, CNRS-MNHN) and P. Reimer (Queen's University Belfast) provided analytical support. We also acknowledge the AST-RX platform, «UMS 2700 Acquisition et Analyse de Données, CNRS-MNHN» for the micro-CT procedure, G. Clément (UMR 7207, CNRS-MNHN), J.-L. Heim, A. Hurel, A.-L. Millan-Brun (UMR 7194, CNRS-MNHN), A. Monaque and the staff of the central library of the MNHN who helped us with the research involving Boule’s archives. Financial support was provided by Sorbonne Université, by the French National Research Agency via the LaScArBx Labex (Project number ANR-10-LABX-52), by the région Aquitaine (through the CHROQUI and NATCH projects), by the European Research Council (grant agreement no. 694707 to S. Pääbo) and the Max Planck Society. DNA sequences generated in this study were deposited in the European Nucleotide Archive under study accession number PRJEB37614. S. Talamo is supported by the European Research Council under the European Union’s Horizon 2020 Research and Innovation Programme (grant agreement No. 803147 RESOLUTION,

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A.B., A.G.-O. designed research, A.B., S.T., C.D., G.G., F.W., I.C., H.F., B.M., M.M. and A.G.-O. performed research, A.B., A.T., S.T., C.D., G.G., F.W., I.C., H.F., J.-J.H., C.L., B.M., M.M., C.S., and A.G.-O. contributed new reagents/analytic tools, A.B., A.T., S.T., C.D., G.G., F.W., I.C., H.F., J.-J.H., C.L., B.M., M.M., C.S., and A.G.-O. analysed data; and A.B., S.T., C.D., G.G., F.W., B.M., M.M., and A.G.-O. wrote the paper.

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Balzeau, A., Turq, A., Talamo, S. et al. Pluridisciplinary evidence for burial for the La Ferrassie 8 Neandertal child. Sci Rep 10, 21230 (2020).

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