Brief communication: Investigation of the semicircular canal variation in the Krapina Neandertals

Previous studies comparing bony labyrinth morphology in geographically‐dispersed samples of Neandertals and modern Homo sapiens (H. sapiens) showed that Neandertals generally have smaller semicircular canals than modern H. sapiens (Hublin et al., 1996 ; Spoor et al., 2003 ; Glantz et al., 2008 ). Here we analyze the morphology of a single group of Neandertal specimens from one locale, the Krapina site, to determine the intraspecific variation in Neandertal semicircular canal sizes. Dimensions of the semicircular canals were collected from computed tomography scans of nine temporal bones. With the rare exception, the dimensions of the semicircular canals in the Krapina sample are similar to those previously reported across a geographically‐dispersed sample of Neandertals, further supporting previous studies that suggest low levels of variation in the semicircular canals for Neandertals. Am J Phys Anthropol 154:302–306, 2014. © 2014 Wiley Periodicals, Inc.     

The medial pterygoid tubercle in the Atapuerca Early and Middle Pleistocene mandibles: Evolutionary implications

Numerous studies have attempted to identify the presence of uniquely derived (autoapomorphic) Neandertal features. Here, we deal with the medial pterygoid tubercle (MTP), which is usually present on the internal face of the ascending ramus of Neandertal specimens. Our study stems from the identification of a hypertrophied tubercle in ATD6‐96, an Early Pleistocene mandible recovered from the TD6 level of the Atapuerca‐Gran Dolina site and attributed to Homo antecessor. Our review of the literature and study of numerous original fossil specimens and high quality replicas confirm that the MTP occurs at a high frequency in Neandertals (ca. 89%) and is also present in over half (ca. 55%) of the Middle Pleistocene Sima de los Huesos (SH) hominins. In contrast, it is generally absent or minimally developed in other extinct hominins, but can be found in variable frequencies (<ca. 25%) in Pleistocene and recent H. sapiens samples. The presence of this feature in ATD6‐96 joins other traits shared by H. antecessor, the SH hominins and Neandertals. Since the TD6 hominins have been attributed either to MIS 21 or to MIS 25, it seems that a suite of assumed derived Neandertal features appeared in the Early Pleistocene, and they should be interpreted as synapomorphies shared among different taxa. We suggest that H. antecessor, the SH hominins and Neandertals shared a common ancestor in which these features appeared during the Early Pleistocene. The presence of the MTP in taxa other than H. neanderthalensis precludes this feature from being a Neandertal autapomorphy. Am J Phys Anthropol 156:102–109, 2015 © 2014 Wiley Periodicals, Inc.     

Reexamination of the immature hominid maxilla from Tangier,Morocco

Reexamination of the immature Upper Pleistocene hominid maxilla from Mugharet el-'Aliya (Tangier), Morocco is undertaken in light of new evidence on the growth and development of Upper Pleistocene hominids. Metric and qualitative comparisons were made with 17 immature Upper Pleistocene maxillae, and with a recent Homo sapiens sapiens sample. No unambiguous criteria for aligning the maxilla with Neandertals were found, although one character, the degree of maxillary flexion on the zygoma, strongly suggests that this child could be a representative of H. s. sapiens. The probable lack of a canine fossa in Mugharet el-'Aliya 1, the primary criterion used previously to align it with Neandertals, cannot be accurately extrapolated to its adult form from this juvenile. The present evidence suggests that it is inappropriate to refer to this fossil as “Neandertal-like” or as a North African “neandertaloid.” Thus, the Tangier maxilla should not be cited as evidence for the presence of Neandertal facial features in North Africa during the Upper Pleistocene. © 1993 Wiley-Liss, Inc.     

A uniquely modern human pattern of endocranial development. Insights from a new cranial reconstruction of the Neandertal newborn from Mezmaiskaya

The globular braincase of modern humans is distinct from all fossil human species, including our closest extinct relatives, the Neandertals. Such adult shape differences must ultimately be rooted in different developmental patterns, but it is unclear at which point during ontogeny these group characteristics emerge.Here we compared internal shape changes of the braincase from birth to adulthood in Neandertals (N = 10), modern humans (N = 62), and chimpanzees (N = 62). Incomplete fossil specimens, including the two Neandertal newborns from Le Moustier 2 and Mezmaiskaya, were reconstructed using reference-based estimation methods. We used 3D geometric morphometrics to statistically compare shapes of virtual endocasts extracted from computed-tomographic scans. Throughout the analysis, we kept track of possible uncertainties due to the missing data values and small fossil sample sizes.We find that some aspects of endocranial development are shared by the three species. However, in the first year of life, modern humans depart from this presumably ancestral pattern of development. Newborn Neandertals and newborn modern humans have elongated braincases, and similar endocranial volumes. During a ‘globularization-phase’ modern human endocasts change to the globular shape that is characteristic for Homo sapiens. This phase of early development is unique to modern humans, and absent from chimpanzees and Neandertals.Our results support the notion that Neandertals and modern humans reach comparable adult brain sizes via different developmental pathways. The differences between these two human groups are most prominent directly after birth, a critical phase for cognitive development.     

Diagnostic differences in mandibular P4 shape between Neandertals and anatomically modern humans

This study uses elliptical Fourier analysis to quantify shape differences observed in the P(4) crown of Neandertals and anatomically modern humans. Previously, P(4) shape was assessed qualitatively, and results suggested marked differences between Neandertals and anatomically modern humans (Bailey [2002] New Anat. 269:148-156). The goal of this study was to investigate the P(4) shape in more detail, quantifying it in order to determine its utility for taxonomic classification and phylogenetic analysis. A comparison of mean shapes confirms that the mesiolingual portion of the P(4) is truncated in Neandertals, and that this produces a distinctively asymmetrical P(4). A randomization test confirms that the shape difference between Neandertals and anatomically modern humans is significant. Principal component and discriminant function analyses indicate that the relative size of the lingual portion of the tooth also affects tooth shape, with the lingual portion of the Neandertal P(4) being narrower than that of anatomically modern humans. Classification of P(4) crown shapes using discriminant functions analysis is far from perfect. While 86.4% of the teeth were correctly classified, classification was much better for anatomically modern humans (98.1%) than it was for Neandertals (65%). Fortunately, crown shape is but one of several diagnostic characters of the P(4) crown. P(4) crown asymmetry can be added to the growing list of dental morphological characters distinguishing Neandertals from anatomically modern humans. Moreover, based on a comparison of mean tooth shapes in fossil and recent humans, symmetry, rather than asymmetry, appears to be the primitive state, and the high frequency of P(4) asymmetry is likely derived in Neandertals.     

The absolute dating of Upper Pleistocene subSaharan fossil hominids and their place in human evolution

In the evolution of anatomically modern man and his subspecies most specialists have concentrated on investigating geographical areas other than Africa as the possible area of origin.In this study 20 fossil hominids and associated faunal remains from South and East Africa were dated by microanalysis, radiocarbon, and amino-acid dating in order to see whether modern man appears later, was sympatric, or even predated Neandertal man.These dates indicate that anatomically modern man occurs sympatrically and possibly even predates the Rhodesian group of Neandertals in Africa. Modern man might also be contemporary to and possibly even predate the occurrence of Neandertal in Europe.This would indicate that modern man did not evolve from but possibly gave rise to the Neandertals as off-shoots.Two possibilities for the evolution of modern man are suggested. First, that Homo sapiens capensis evolved about 90,000 to 100,000 years ago from possibly Homo erectus by way of a “basic” Homo sapiens and later gave rise to Homo sapiens rhodesiensis, Homo sapiens afer, and possibly Homo sapiens palestinus around 50,000 years ago with Homo neanderthalensis and Homo sapiens capensis evolving separately from Homo erectus. In this case Homo neanderthalensis would be a different species from Homo sapiens which includes Homo sapiens capensis, Homo sapiens rhodesiensis, Homo sapiens afer, and possibly Homo sapiens palestinus.Secondly, Homo sapiens capensis evolved by way of a “basic” Homo sapiens with Homo sapiens rhodesiensis and Homo sapiens palestinus branching off from Homo sapiens capensis around 50,000 years ago. Before that, around 90,000 to 100,000 years ago Homo sapiens capensis evolved first and was then followed by Homo sapiens neanderthalensis from a “basic” Homo sapiens stock, but diverged. This means, all Neandertals, Homo sapiens capensis, Homo sapiens sapiens and Homo sapiens afer can be considered as subspecies of Homo sapiens.The author favors the first scheme since on relative dating grounds the existence of Neandertal man in Europe before the earliest date of Homo sapiens capensis and a “basic” Homo sapiens seems to be fairly well documented. Irrespective of either one of these possibilities, modern man evolved in Africa and seems to have migrated into Europe and other parts of the world.New absolute dating techniques are mentioned in detail like the new radiocarbon-collagen method and amino acid dating.     

Volumetric and asymmetry determinations on recent hominid endocasts: Spy I and II,Djebel Ihroud I,and the salè Homo erectus specimens,with some notes on neandertal brain size

Full brain endocast reconstructions of the Neandertals, Spy I and II, Djebel Ihroud I, and the Homo erectus specimen from Salè, Morocco have yielded accurate volumes. Spy I = 1,305 ml; Spy II = 1,553 ml; Djebel Ihroud I = 1,305 ml; Salè = 880 ml. While there are no remarkable gyral and sulcal patterns one can delineate, the brain endocasts do show evidence of left-occipital, right-frontal petalias, suggesting right-handedness, and possibly human cognitive specialization, involving symbol processing and visuospatial integration. Some speculations regarding Neandertal brain size are also offered, in which it is suggested that their possibly larger brain sizes were related to greater muscularity than in modern Homo sapiens.     

Stature estimation from complete long bones in the Middle Pleistocene humans from the Sima de los Huesos, Sierra de Atapuerca (Spain)

Systematic excavations at the site of the Sima de los Huesos (SH) in the Sierra de Atapuerca (Burgos, Spain) have allowed us to reconstruct 27 complete long bones of the human species Homo heidelbergensis. The SH sample is used here, together with a sample of 39 complete Homo neanderthalensis long bones and 17 complete early Homo sapiens (Skhul/Qafzeh) long bones, to compare the stature of these three different human species. Stature is estimated for each bone using race- and sex-independent regression formulae, yielding an average stature for each bone within each taxon. The mean length of each long bone from SH is significantly greater (p < 0.05) than the corresponding mean values in the Neandertal sample. The stature has been calculated for male and female specimens separately, averaging both means to calculate a general mean. This general mean stature for the entire sample of long bones is 163.6 cm for the SH hominins, 160.6 cm for Neandertals and 177.4 cm for early modern humans. Despite some overlap in the ranges of variation, all mean values in the SH sample (whether considering isolated bones, the upper or lower limb, males or females or more complete individuals) are larger than those of Neandertals. Given the strong relationship between long bone length and stature, we conclude that SH hominins represent a slightly taller population or species than the Neandertals. However, compared with living European Mediterranean populations, neither the Sima de los Huesos hominins nor the Neandertals should be considered ‘short’ people. In fact, the average stature within the genus Homo seems to have changed little over the course of the last two million years, since the appearance of Homo ergaster in East Africa. It is only with the emergence of H. sapiens, whose earliest representatives were ‘very tall’, that a significant increase in stature can be documented.     

New perspectives on the “Proto-cromagnons” from Israel

The present paper deals with the two identifiedHomo sapiens groups in the Middle Palaeolithic from the Near East, the Neandertals and the Modern Humans. Their main morphological characteristics are discussed, comparing also both populations, one with another, as well as with the European Neandertals or Predmost III. The data confirm the presence in the Levant of Near Eastern Neandertal and Modern Human lineages from at least 150 Ky., relating the most ancient documents, respectively, to Tabun I and Zuttiyeh individuals. The coexistence of both human groups, having the same cultural background, along the whole Middle Palaeolithic is demonstrated, while the possibility of interbreeding is not excluded.     

Lower limb bone structure of Middle Pleistocene hominins from the Caune de l’Arago (Tautavel,France): Evolutionary and functional comparison with the penecontemporaneous hominins of Sima de los Huesos (Atapuerca,Spain)

The Caune de l’Arago (Arago) and Sima de los Huesos (Sima) human bones from the European Middle Pleistocene are penecontemporaneous, although the Sima hominins are closely related to Neandertal, and Arago hominins present more archaic features. In previous and in press studies, the cross-sectional geometric properties (CSG) of lower limb bones of Arago and Sima have been studied separately without comparative analyses. Here, in order to bridge this gap, we use the same criteria for both samples to highlight evolutionary affinities and to compare their level and pattern of mobility. This study focuses on the femur, fibula and tibia from Arago and Sima with references to fossils from the sites of Trinil, Zhoukoudian and Lazaret, and ancient and recent Homo sapiens (including athletes and non-athletes). We analyze the cross-sectional areas, biomechanical bone “shape” indices (Ix/Iy, Imax/Imin) and pattern of cortical bone distribution. All lower limb bones from Arago have noticeably high to very high relative cortical areas and low to very low medullary areas. The overall femoral pattern in Arago, like Sima, is similar to that of Middle Pleistocene hominins (e.g., low femoral shape indices, Ix/Iy) and Neandertals (e.g., large cross-sectional size). However, the femoral midshaft in Sima presents prominent posteromedial cortical thickening, as a result of a spiral cortical reinforcement along the medial side of the diaphysis. This characteristic is specific to Neandertal and some Middle Pleistocene hominins. In contrast, the midshaft femoral pattern in Arago is close to that of some Homo erectus. We also note that the femoral cross-sectional size and relative cortical area in Arago differ drastically to the small size and low relative cortical area of Lazaret and Trinil hominins. The very high shape index at midshaft (i.e., high Imax/Imin) of the Arago tibia is observed in ancient H. sapiens and runners; the tibial posterior “pilaster” is found in Neandertals and ancient H. sapiens; and the flat or convex tibial faces are similar to Neandertals. Furthermore, the Arago fibulas show marked fibular posterolateral cortical reinforcement with low anteroposterior strengthening. These leg features (tibia, fibula) are also found in some Sima hominins (but not in all individuals). Consequently, this study confirms the presence of archaic features in Arago and the close evolutionary relationship between Sima and Neandertal. This proposition is mainly based on the femoral midshaft pattern influenced by the pelvofemoral complex, considered to be substantially genetically controlled. The leg functional analysis highlights a high level of mobility and travelling in uneven terrains or in mountainous areas in Arago, consistent with known environments and hunting practices. Previously, an analogous hypothesis was proposed put forward for Sima hominins.     

Absolute and relative endocranial size in Neandertals and later Pleistocene Homo

Eurasian Neandertals encompass the entire observed range of recent and fossil Homo sapiens in absolute, but not relative endocranial volume, and Neandertals attest an average EQ significantly lower than their Upper Pleistocene successors. While the cognitive, social, and evolutionary implications of this phenomenon have been emphasised, the statistical basis of a mean inference of EQ in the Neandertal hypodigm has not been appropriately demonstrated. A demonstrable male bias in the available postcranial, not cranial, series has skewed perceptions of Neandertal brain-to-body size scaling towards a rejection of the null hypothesis. A simple resolution to this problem is a concise assessment of paired associated covariates against a suitable recent human comparator series. Permutations of Fisher's z and Student's t statistics are valid metrics in tests of significance in single datum hypotheses.     

The place of Neandertals in the evolution of hominid patterns of growth and development

This study uses the two developmental fields of dental maturation and femoral growth to determine if the pattern of growth and development in Neandertals (archaic Homo sapiens) was intermediate between that of Homo erectus and recent modern humans. Specimens used in the analysis included Neandertals and Upper Palaeolithic early modern Homo sapiens from Europe and individuals from two recent modern human populations. Ontogenetic data for the H. erectus adolescent KNM-WT 15000 and for Gorilla gorilla were included for comparison. Previous reports have indicated that H. erectus demonstrates a pattern of ontogeny characterized by earlier and more rapid linear growth than in modern humans. Results reported here demonstrate that Upper Paleolithic early modern Homo sapiens display a growth trajectory indistinguishable from that of recent modern humans. The pattern of Neandertal ontogeny is not intermediate between the pattern displayed in H. erectus and the derived pattern seen in the modern reference samples and the early modern H. sapiens sample. The Neandertal growth trajectory is consistent with either slow linear growth or advanced dental development.     

Calcaneus length determines running economy: implications for endurance running performance in modern humans and Neandertals

The endurance running (ER) hypothesis suggests that distance running played an important role in the evolution of the genus Homo. Most researchers have focused on ER performance in modern humans, or on reconstructing ER performance in Homo erectus, however, few studies have examined ER capabilities in other members of the genus Homo. Here, we examine skeletal correlates of ER performance in modern humans in order to evaluate the energetics of running in Neandertals and early Homo sapiens. Recent research suggests that running economy (the energy cost of running at a given speed) is strongly related to the length of the Achilles tendon moment arm. Shorter moment arms allow for greater storage and release of elastic strain energy, reducing energy costs. Here, we show that a skeletal correlate of Achilles tendon moment arm length, the length of the calcaneal tuber, does not correlate with walking economy, but correlates significantly with running economy and explains a high proportion of the variance (80%) in cost between individuals. Neandertals had relatively longer calcaneal tubers than modern humans, which would have increased their energy costs of running. Calcaneal tuber lengths in early H. sapiens do not significantly differ from those of extant modern humans, suggesting Neandertal ER economy was reduced relative to contemporaneous anatomically modern humans. Endurance running is generally thought to be beneficial for gaining access to meat in hot environments, where hominins could have used pursuit hunting to run prey taxa into hyperthermia. We hypothesize that ER performance may have been reduced in Neandertals because they lived in cold climates.     

Calvarial shape variation among Middle Pleistocene hominins: An application of surface scanning in palaeoanthropology

The increasing availability of 3D data and tools offers new analytical perspectives in palaeoanthropology, such as the quantitative testing of opposing phylogenetic scenarios. Using optical surface scan data and geometric morphometric techniques, this study explores calvarial shape variation in the “Middle Pleistocene muddle”. The morphological variability between H. erectus on the one hand and H. sapiens/neanderthalensis on the other has long remained obscure: opposing views have attributed the known specimens to any of the three species and possibly one or two more. A large number of landmarks and semilandmarks was extracted from the braincase and the face, in order to quantify the calvarial shape differences among species and key fossils. The results are incompatible with the hypothesis that H. rhodesiensis is the exclusive ancestor of H. sapiens, and offer only weak support for an exclusively European ancestor of Neandertals.     

Zonal plant communities of the Ribesalbes‐Alcora Basin (La Rinconada mine,eastern Spain) during the early Miocene

Changes in lobule morphology in Radula subgenus Cladoradula show liverworts have the capacity for dramatic, relatively rapid morphological change by heterochrony. In individuals of R. bipinnata, R. boryana and R. tenax, lobules on secondary and tertiary shoots are progenetic with respect to lobules on primary shoots, in that the slope of the relationship between growth duration and shape does not change. However, in R. campanigera, lobules on secondary and tertiary branches exhibit different slopes from primary branches, but have the same growth duration, a pattern consistent with neoteny. The trajectory of allometric growth is extended or truncated in different species compared with outgroup and ancestral nodes. Changes in duration of lobule growth explain 85% of variation in lobule shape between species. Species are related by relatively shallow nodes in the crown of the Radula subgenus Cladoradula clade, suggesting that divergence and associated heterochronic changes have occurred relatively recently. The rapid morphological diversification in the crown contrasts with the relative stasis between the ancestral node and R. brunnea, the outgroup used in this analysis. A robust primary axis may be required to hold shoots away from vertical surfaces to maximize light interception, and hypermorphosis in lobule ontogeny could be a by‐product of the longer growth durations required to build axes sufficiently large to perform this structural role. Alternatively, the large auriculate lobules could function in external water transport systems by providing continuity of surfaces for solute transport via capillary action. © 2013 The Linnean Society of London, Botanical Journal of the Linnean Society, 2013, 173 , 153–175.     

Fossil human remains from Bolomor Cave (Valencia, Spain)

Systematic excavations carried out since 1989 at Bolomor Cave have led to the recovery of four Pleistocene human fossil remains, consisting of a fibular fragment, two isolated teeth, and a nearly complete adult parietal bone. All of these specimens date to the late Middle and early Late Pleistocene (MIS 7-5e). The fibular fragment shows thick cortical bone, an archaic feature found in non-modern (i.e. non-Homo sapiens) members of the genus Homo. Among the dental remains, the lack of a midtrigonid crest in the M₁ represents a departure from the morphology reported for the majority of Neandertal specimens, while the large dimensions and pronounced shoveling of the marginal ridges in the C¹ are similar to other European Middle and late Pleistocene fossils. The parietal bone is very thick, with dimensions that generally fall above Neandertal fossils and resemble more closely the Middle Pleistocene Atapuerca (SH) adult specimens. Based on the presence of archaic features, all the fossils from Bolomor are attributed to the Neandertal evolutionary lineage.     

Zuttiyeh face: A view from the east

We analyze the phylogenetic position of the frontofacial fragment from Zuttiyeh, Israel. This specimen is dated to the Middle Pleistocene (the latest estimate is between 250 and 350 kyr) and is associated with the Acheulo-Yabrudian, which makes it the oldest cranium from the region. It has been previously regarded as a Neandertal, and early “anatomically modern Homo sapiens,” and a generalized specimen ancestral to both. These different phylogenetic interpretations of its features have a historic basis but in our view also result from a confusion of grade and intraspecies clade as valid sources of variation. We show here that generally the differences that distinguish Zuttiyeh from Neandertals are similarities it shares with the Zhoukoudian remains. These similarities involve a unique combination of features, and suggest the possibility of an ancestral relationship. It is less likely that Middle Pleistocene remains from Europe or sub-Saharan Africa are uniquely or significantly ancestral to Zuttiyeh. An accurate understanding of the relationship between populations of eastern and western Asia is important for resolving the more general questions surrounding the position of the Upper Pleistocene Levant populations in human evolution, including (1) whether there are significantly different contemporary Mousterian populations in the Upper Pleistocene, (2) whether Neandertals are clearly intrusive in the region, and (3) whether there is an early appearance of (what many workers call) “anatomically modern Homo sapiens.” The hypothesis of a recent unique African ancestry for all modern humans is disproved by our study, which shows Asia as a significant source area for at least some living populations. © 1993 Wiley-Liss, Inc.     

Changes in stand composition and structure between 1981 and 1996 in four Front Range plant communities in Colorado

We measured leaf distribution, crown shape, and biomass allocation patterns in open-grown saplings of three tree species (Cedrela odorata, Cordia alliodora, and Hyeronima alchorneoides) that differed in above-ground architecture and successional status. The objectives were to: (1) analyze the relationship between crown structure and biomass allocation in free-growing juveniles and (2) assess whether predictions that relate crown structure and biomass distribution of adult individuals can be applied to noncompeting saplings. Significant differences in crown structure and biomass allocation were found among the three species. Mean dry biomass was 990 g in Cedrela, 665 g, in Cordia, and 1281 g in Hyeronima. Cedrela allocated a greater proportion of biomass into roots than the other two species. We observed no distinct pattern of foliage angle, and no evidence of decrease in crown construction efficiency with tree size. Predictions stated by other authors for mature individuals partially explained the relationships between biomass allocation and morphological variables of non-competing saplings. We proposed two alternative biomass allocation patterns: (1) in open conditions saplings of early successional species exhibit structural characteristics more adapted for high light levels than gap-dependent species, and (2) early successional species have lower cost-benefit ratio for biomass construction and higher foliar efficiency than late successional ones. In general, crown morphometric characteristics and biomass distribution patterns of the three species studied corresponded with the two proposed patterns.     

Neandertals and moderns mixed,and it matters

Twenty‐five years ago, the Middle‐to‐Upper Paleolithic transition in Europe could be represented as a straightforward process subsuming both the emergence of symbolic behavior and the replacement of Neandertals by modern humans. The Aurignacian was a proxy for the latter, during which enhanced cognitive capabilities explained ornaments and art. The few instances of Neandertal symbolism were deemed to long postdate contact and dismissed as “imitation without understanding,” if not geological contamination. Such views were strengthened by the recent finding that, in southern Africa, several features of the European Upper Paleolithic, including bone tools, ornaments, and microliths, emerged much earlier. Coupled with genetic suggestions of a recent African origin for extant humans, fossil discoveries bridging the transition between “archaics” and “moderns” in the realm of anatomy (Omo‐Kibish, Herto) seemingly closed the case. Over the last decade, however, taphonomic critiques of the archeology of the transition have made it clear that, in Europe, fully symbolic sapiens behavior predates both the Aurignacian and moderns. And, in line with evidence from the nuclear genome rejecting strict replacement models based on mtDNA alone, the small number of early modern specimens that passed the test of direct dating present archaic features unknown in the African lineage, suggesting admixture at the time of contact. In the realm of culture, the archeological evidence also supports a Neandertal contribution to Europe's earliest modern human societies, which feature personal ornaments completely unknown before immigration and are characteristic of such Neandertal‐associated archeological entities as the Châtelperronian and the Uluzzian. The chronometric data suggest that, north of the Ebro divide, the entire interaction process may have been resolved within the millennium centered around 42,000 calendar years ago. Such a rapid absorption of the Neandertals is consistent with the size imbalance between the two gene reservoirs and further supports significant levels of admixture.     

Morphological and functional aspects of the temporal bone articular tubercle morphology inHomo erectus andHomo sapiens

The morphological variability of the temporal articular tubercle was studied inHomo erectus andHomo sapiens. Five configurations have been defined. There is a high heterogeneity amongHomo erectus. The Neandertal lineage and that leading toHomo sapiens sapiens are more homogenous, each of them exhibits a high frequency of one configuration. This study has also focused on the functional implications of this variation. A theoretical approach to two different configurations of the articular tubercle is considered in the same bony, muscular and ligamentary context. This suggests that the configuration which consists of a transverse concavity is, for the mandible depression, concomitant with a slight functional disadvantage in comparison with the cylindrical configuration. It appears that a midfacial projection allows for a compensation of this disadvantage. It is concluded that this model can be proposed for Neandertals which present a very concave articular tubercle and a typical midfacial projection.