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Significance The new species Homo naledi was discovered in 2013 in a remote cave chamber of the Rising Star cave system, South Africa. This species survived until between 226,000 and 335,000 y ago, placing it in continental Africa at the same time as the early ancestors of modern humans were arising. Yet, H. naledi was strikingly primitive in many aspects of its anatomy, including the small size of its brain. Here, we have provided a description of endocast anatomy of this primitive species. Despite its small brain size, H. naledi shared some aspects of human brain organization, suggesting that innovations in brain structure were ancestral within the genus Homo .

Little is known about how occipital lobe asymmetry, width, and height interact to contribute to the operculation of the posterior parietal lobe, despite the utility of knowing this for understanding the relative reduction in the size of the occipital lobe and the increase in the size of the posterior parietal lobe during human brain evolution. Here, we use linear measurements taken on 3D virtual brain surfaces obtained from 83 chimpanzees to study these traits as they apply to operculation of the posterior occipital parietal arcus or bridging gyrus. Asymmetry in this bridging gyrus visibility provides a unique opportunity to study both the human ancestral and human equivalently normal condition in the same individual. Our results show that all three traits (occipital lobe asymmetry, width, and height) are related to this operculation and bridging gyrus visibility but width and not height is the best predictor, against expectations, suggesting that relative reduction of the occipital lobe and exposure of the posterior parietal is a complex phenomenon.

The large brain and small postcanine teeth of modern humans are among our most distinctive features, and trends in their evolution are well studied within the hominin clade. Classic accounts hypothesize that larger brains and smaller teeth coevolved because behavioral changes associated with increased brain size allowed a subsequent dental reduction. However, recent studies have found mismatches between trends in brain enlargement and posterior tooth size reduction in some hominin species. We use a multiple-variance Brownian motion approach in association with evolutionary simulations to measure the tempo and mode of the evolution of endocranial and dental size and shape within the hominin clade. We show that hominin postcanine teeth have evolved at a relatively consistent neutral rate, whereas brain size evolved at comparatively more heterogeneous rates that cannot be explained by a neutral model, with rapid pulses in the branches leading to later Homo species. Brain reorganization shows evidence of elevated rates only much later in hominin evolution, suggesting that fast-evolving traits such as the acquisition of a globular shape may be the result of direct or indirect selection for functional or structural traits typical of modern humans.

Labial striations on the anterior teeth have been documented in numerous European pre-Neandertal and Neandertal fossils and serve as evidence for handedness. OH-65, dated at 1.8 mya, shows a concentration of oblique striations on, especially, the left I1 and right I1, I2 and C1, which signal that it was right-handed. From these patterns we contend that OH-65 was habitually using the right hand, over the left, in manipulating objects during some kind of oral processing. In living humans right-handedness is generally correlated with brain lateralization, although the strength of the association is questioned by some. We propose that as more specimens are found, right-handedness, as seen in living Homo, will most probably be typical of these early hominins.

Objectives The Homo erectus-like cranium from Buia (UA 31) was found in the Eritrean Danakil depression and dated to 1 million years. Its outer morphology displays archaic traits, as well as distinctive and derived characters. The present study provides the description and metric comparison of its endocranial anatomy. Materials and Methods UA 31 was originally filled by a diffuse concretion. Following its removal and cleaning, the endocast (995 cc) was reconstructed after physical molding and digital scan. Its morphology is here compared with specimens belonging to different human taxa, taking into account endocranial metrics, cortical traits, and craniovascular features. Results The endocast is long and narrow when compared to the H. erectus/ergaster hypodigm, although its proportions are compatible with the morphology displayed by all archaic and medium-brained human species. The occipital areas display a pronounced bulging, the cerebellum is located in a posterior position, and the middle meningeal vessels are more developed in the posterior regions. These features are common among specimens attributed to H. erectus s.l., particularly the Middle Pleistocene endocasts from Zhoukoudian. The parietal lobes are markedly bossed. This lateral bulging is associated with the lower parietal circumvolutions, as in other archaic specimens. This pronounced parietal curvature is apparently due to a narrow cranial base, more than to wider parietal areas. Conclusions The endocast of UA 31 shows a general plesiomorphic phenotype, with some individual features (e.g., dolichocephaly and rounded lower parietal areas) which confirm a remarkable degree of morphological variability within the H. erectus/ergaster hypodigm. Am J Phys Anthropol 160:458–468, 2016. © 2016 Wiley Periodicals, Inc.

International audience; The study of brain structural asymmetries as anatomical substrates of functional asymmetries in extant humans, great apes, and fossil hominins is of major importance in understanding the structural basis of modern human cognition. We propose methods to quantify the variation in size, shape and bilateral asymmetries of the third frontal convolution (or posterior inferior frontal gyrus) among recent modern humans, bonobos and chimpanzees, and fossil hominins using actual and virtual endocasts. These methodological improvements are necessary to extend previous qualitative studies of these features. We demonstrate both an absolute and relative bilateral increase in the size of the third frontal convolution in width and length between Pan species, as well as in hominins. We also observed a global bilateral increase in the size of the third frontal convolution across all species during hominin evolution, but also non-allometric intra-group variations independent of brain size within the fossil samples. Finally, our results show that the commonly accepted leftward asymmetry of Broca's cap is biased by qualitative observation of individual specimens. The trend during hominin evolution seems to be a reduction in size on the left compared with the right side, and also a clearer definition of the area. The third frontal convolution considered as a whole projects more laterally and antero-posteriorly in the right hemisphere. As a result, the left 'Broca's cap' looks more globular and better defined. Our results also suggest that the pattern of brain asymmetries is similar between Pan paniscus and hominins, leaving the gradient of the degree of asymmetry as the only relevant structural parameter. As the anatomical substrate related to brain asymmetry has been present since the appearance of the hominin lineage, it is not possible to prove a direct relationship between the extent of variations in the size, shape, and asymmetries of the third frontal convolution and the origin of language in hominins.

Paleoneurology is an important field of research within human evolution studies. Variations in size and shape of an endocast help to differentiate among fossil hominin species whereas endocranial asymmetries are related to behavior and cognitive function. Here we analyse variations of the surface of the frontal, parieto-temporal and occipital lobes among different species of Homo , including 39 fossil hominins, ten fossil anatomically modern Homo sapiens and 100 endocasts of extant modern humans. We also test for the possible asymmetries of these features in a large sample of modern humans and observe individual particularities in the fossil specimens. This study contributes important new information about the brain evolution in the genus Homo . Our results show that the general pattern of surface asymmetry for the different regional brain surfaces in fossil species of Homo does not seem to be different from the pattern described in a large sample of anatomically modern H. sapiens , i.e., the right hemisphere has a larger surface than the left, as do the right frontal, the right parieto-temporal and the left occipital lobes compared with the contra-lateral side. It also appears that Asian Homo erectus specimens are discriminated from all other samples of Homo , including African and Georgian specimens that are also sometimes included in that taxon. The Asian fossils show a significantly smaller relative size of the parietal and temporal lobes. Neandertals and anatomically modern H. sapiens , who share the largest endocranial volume of all hominins, show differences when considering the relative contribution of the frontal, parieto-temporal and occipital lobes. These results illustrate an original variation in the pattern of brain organization in hominins independent of variations in total size. The globularization of the brain and the enlargement of the parietal lobes could be considered derived features observed uniquely in anatomically modern H. sapiens .

The designation of Homo floresiensis as a new species derived from an ancient population is controversial, because the type specimen, LB1, might represent a pathological microcephalic modern Homo sapiens . Accordingly, two specific craniometric ratios (relative frontal breadth and cerebellar protrusion) were ascertained in 21 microcephalic infants and children by using MRI. Data on 118 age-equivalent control (normocephalic) subjects were collected for comparative purposes. In addition, the same craniometric ratios were determined on the endocasts of 10 microcephalic individuals, 79 normal controls (anatomically modern humans), and 17 Homo erectus specimens. These ratios were then compared with those of two LB1 endocasts. The findings showed that the calculated cerebral/cerebellar ratios of the LB1 endocast [Falk D, et al. (2007) Proc Natl Acad Sci USA 104:2513–2518] fall outside the range of living normocephalic individuals. The ratios derived from two LB1 endocasts also fall largely outside the range of modern normal human and H. erectus endocasts and within the range of microcephalic endocasts. The findings support but do not prove the contention that LB1 represents a pathological microcephalic Homo sapiens rather than a new species, (i.e., H. floresiensis ).

The Taung endocast is one of the best-preserved and most important known in paleoanthropology. Although the endocast is undistorted and preserves distinctive landmarks, Taung has proved a difficult endocast, because it is only about 60% complete. To reconstruct Taung it is necessary to first use the available anatomical landmarks to define the midline of the endocast. It is only with a proper description of the midline that it is possible to reconstruct the endocast and obtain an accurate measurement of Taung's endocranial volume. Holloway (Science 168 (1970) 966–968) determined a conservative estimate for Taung of 404 ml. More recently this estimate has been revised downward by Falk and Clarke (Am J Phys Anthropol 134 (2007) 529–534) to 382 ml, giving Taung the smallest endocast for A. africanus. Certain challenges exist with the reconstruction of any endocast, particularly a hemi-endocast such as Taung. A virtual reconstruction of Taung must assume perfect symmetry, a feature called into question here in Taung's most recent reconstruction by Falk and Clarke (2007). Holloway's (1970) reconstruction of Taung provides a guidepost for a conservative approach to endocast reconstructions, and the most reliable measurement of Taung's true endocranial volume. Am J Phys Anthropol, 2011. © 2011 Wiley-Liss, Inc.

Minor controversies notwithstanding, the evolution of the human brain has been an intermingled composite of allometric and nonallometric increases of brain volume and reorganizational events such as the reduction of primary visual cortex and a relative increase in both posterior association and (most probably) prefrontal cortex, as well as increased cerebral asymmetries, including Broca's and Wernicke's regions, with some of these changes already occurring in australopithecine times. As outlined in Holloway (1967), positive feedback (amplification-deviation) has been a major mechanism in size increases. Exactly how this mélange of organs evolved will require many more paleontological discoveries with relatively intact crania, an unraveling of the genetic bases for both brain structures and their relationship to behaviors, and a far more complete picture of how the brain varies between male and female and among different populations throughout the world. After all, the human brain is still evolving, but for how long is quite uncertain.

The trigeminal motor (Vmo), facial (VII), and hypoglossal (XII) nuclei of the brainstem comprise the final common output for neural control of most orofacial muscles. Hence, these cranial motor nuclei are involved in the production of adaptive behaviors such as feeding, facial expression, and vocalization. We measured the volume and Grey Level Index (GLI) of Vmo, VII, and XII in 47 species of primates and examined these nuclei for scaling patterns and phylogenetic specializations. Allometric regression, using medulla volume as an independent variable, did not reveal a significant difference between strepsirrhines and haplorhines in the scaling of Vmo volume. In addition, correlation analysis using independent contrasts did not find a relationship between Vmo size or GLI and the percent of leaves in the diet. The scaling trajectory of VII volume, in contrast, differed significantly between suborders. Great ape and human VII volumes, furthermore, were significantly larger than predicted by the haplorhine regression. Enlargement of VII in these taxa may reflect increased differentiation of the facial muscles of expression and greater utilization of the visual channel in social communication. The independent contrasts of VII volume and GLI, however, were not correlated with social group size. To examine whether the human hypoglossal motor system is specialized to control the tongue for speech, we tested human XII volume and GLI for departures from nonhuman haplorhine prediction lines. Although human XII volumes were observed above the regression line, they did not exceed prediction intervals. Of note, orang-utan XII volumes had greater residuals than humans. Human XII GLI values also did not differ from allometric prediction. In sum, these findings indicate that the cranial orofacial motor nuclei evince a mosaic of phylogenetic specializations for innervation of the facial muscles of expression in the context of a generally conservative scaling relationship with respect to medulla size.

Since Dart’s analysis of the Taung skull in1925 in Nature, there has been controversy surrounding the presence of a clearly defined lunate sulcus (LS) in the australopithecines, marking the anterior extent of primary visual cortex (PVC). An anterior position signifies that the LS is in an ape-like position, such as found in Pan troglodytes. A posterior position is a more human-like characteristic (autapomorphy). If the latter occurred in Australopithecus, then the cerebral cortex underwent some neurological reorganization prior to brain enlargement, thus occurring earlier than the emergence of the genus Homo. The endocast of the Stw 505 specimen from Sterkfontein, South Africa, shows an unmistakably posterior placement of the LS. The early hominid brain was reorganized at least by the time of Australopithecus africanus, thus vindicating Dart’s early assessment. To cite this article: R.L. Holloway, C. R. Palevol 3 (2004).

Social life in anthropoid primates is mediated by interindividual communication, involving movements of the orofacial muscles for the production of vocalization and gestural expression. Although phylogenetic diversity has been reported in the auditory and visual communication systems of primates, little is known about the comparative neuroanatomy that subserves orofacial movement. The current study reports results from quantitative image analysis of the region corresponding to orofacial representation of primary motor cortex (Brodmann’s area 4) in several catarrhine primate species (Macaca fascicularis, Papio anubis, Pongo pygmaeus, Gorilla gorilla, Pan troglodytes, and Homo sapiens) using the Grey Level Index method. This cortical region has been implicated in the execution of skilled motor activities such as voluntary facial expression and human speech. Density profiles of the laminar distribution of Nissl-stained neuronal somata were acquired from high-resolution images to quantify cytoarchitectural patterns. Despite general similarity in these profiles across catarrhines, multivariate analysis showed that cytoarchitectural patterns of individuals were more similar within-species versus between-species. Compared to Old World monkeys, the orofacial representation of area 4 in great apes and humans was characterized by an increased relative thickness of layer III and overall lower cell volume densities, providing more neuropil space for interconnections. These phylogenetic differences in microstructure might provide an anatomical substrate for the evolution of greater volitional fine motor control of facial expressions in great apes and humans.

This report presents data regarding the brain structure of mountain gorillas (Gorilla beringei beringei) in comparison with other great apes. Magnetic resonance (MR) images of three mountain gorilla brains were obtained with a 3T scanner, and the volume of major neuroanatomical structures (neocortical gray matter, hippocampus, thalamus, striatum, and cerebellum) was measured. These data were included with our existing database that includes 23 chimpanzees, three western lowland gorillas, and six orang-utans. We defined a multidimensional space by calculating the principal components (PCs) from the correlation matrix of brain structure fractions in the well-represented sample of chimpanzees. We then plotted data from all of the taxa in this space to examine phyletic variation in neural organization. Most of the variance in mountain gorillas, as well as other great apes, was contained within the chimpanzee range along the first two PCs, which accounted for 61.73% of the total variance. Thus, the majority of interspecific variation in brain structure observed among these ape taxa was no greater than the within-species variation seen in chimpanzees. The loadings on PCs indicated that the brain structure of great apes differs among taxa mostly in the relative sizes of the striatum, cerebellum, and hippocampus. These findings suggest possible functional differences among taxa in terms of neural adaptations for ecological and locomotor capacities. Importantly, these results fill a critical gap in current knowledge regarding great ape neuroanatomical diversity. Am. J. Primatol. 63:149–164, 2004. © 2004 Wiley-Liss, Inc.

The neocortex of primates contains several distinct neuron subtypes. Among these, Betz cells of primary motor cortex and Meynert cells of primary visual cortex are of particular interest for their potential role in specialized sensorimotor adaptations of primates. Betz cells are involved in setting muscle tone prior to fine motor output and Meynert cells participate in the processing of visual motion. We measured the soma volumes of Betz cells, Meynert cells, and adjacent infragranular pyramidal neurons in 23 species of primate and two species of non-primate mammal (Tupaia glis and Pteropus poliocephalus) using unbiased stereological techniques to examine their allometric scaling relationships and socioecological correlations. Results show that Betz somata become proportionally larger with increases in body weight, brain weight, and encephalization whereas Meynert somata remain a constant proportion larger than other visual pyramidal cells. Phylogenetic variance in the volumetric scaling of these neuronal subtypes might be related to species-specific adaptations. Enlargement of Meynert cells in terrestrial anthropoids living in open habitats, for example, might serve as an anatomical substrate for predator detection. Modification of the connectional and physiological properties of these neurons could constitute an important evolutionary mode for species-specific adaptation.

A new fossil calvaria, Sambungmacan 3 (Sm 3), described in New Fossil Hominid Calvaria From Indonesia--Sambungmacan 3 by Marquez et al., this volume, yields one of the most advanced and complete endocasts yet recovered from Java. This communication provides a thorough interpretation of the external anatomical landmarks observable on Sm 3. Using computer tomography (CT) and traditional morphological measurements, our comparative paleoneurological analyses show that while Sm 3 has a mosaic of features that are similar to both Indonesian and Chinese H. erectus, it also possesses significant characters reminiscent of later hominins. These include a greater degree of asymmetry characterized by a possible left-occipital, right-frontal petalial pattern, left-right volumetric cerebral asymmetry, and marked asymmetry in Broca's cap. Moreover, the frontal lobe offers a more rounded, shortened appearance in contrast to the flat, elongated appearance of other Indonesian fossils (e.g., Sangiran 17). Another unique trait is exhibited in the transverse plane where the widest breadth of Sm 3 occurs more superiorly than in other Indonesian H. erectus. Thus, the endocast of Sm 3 presents a unique morphology not seen previously in the hominin fossil record. While the strong modern human characteristics in this endocast may not represent a particular ancestry, they do allow us to recognize a new dimension of the remarkable variation in Indonesian Homo erectus.

The midsagittal area and other morphological measures were taken on the corpus callosum of four different species of primate: Macaca mulatta, M. fascicularis, Callithrix jacchus, and Saguinus oedipus. The first two species are strongly dimorphic, whereas the New World forms show little dimorphism with regard to overall body size, canines, and brain weight. Neither total corpus callosal area (TOTALCC), or other parts of the corpus callosum (CC) showed any significant sexual dimorphism in any of the primate species sampled. Only in M. mulatta did a sexual dimorphism appear to be significant. In males of this species, the dorsoventral width of the splenium was larger than in females. In addition, the anterior commissure (ANTCOMM) evinced no sexual dimorphism in the different species. Brain weight was significantly dimorphic in only M. mulatta, and when ratio data were used to correct for brain weight, no significant differences were found in the corpus callosum. This is in contrast to Homo sapiens, where the relative size of the CC has been reported to be larger in females, and particularly so in the posterior, or splenial portion of the CC. Correlation coefficients were calculated for the various variables within each species. In general, most of the callosal measures are significantly inter-correlated, although the exact pattern varies for each species. Thus, unlike Homo sapiens, or pongids such as Gorilla and Pan, neither New nor Old World monkeys show any striking evidence for sexual dimorphism in the corpus callosum.

Data do exist to support the fact that the corpus callosum is relatively larger in women than in men. The corpus callosum is an integral part of the brain, and contrary to Fitch & Denenberg's examples of “pseudostatistics,” is not an extrinsic structure when determining its relative size.

The anatomic pattern and left hemisphere size predominance of the planum temporale, a language area of the human brain, are also present in chimpanzees ( Pan troglodytes ). The left planum temporale was significantly larger in 94 percent (17 of 18) of chimpanzee brains examined. It is widely accepted that the planum temporale is a key component of Wernicke's receptive language area, which is also implicated in human communication-related disorders such as schizophrenia and in normal variations such as musical talent. However, anatomic hemispheric asymmetry of this cerebrocortical site is clearly not unique to humans, as is currently thought. The evolutionary origin of human language may have been founded on this basal anatomic substrate, which was already lateralized to the left hemisphere in the common ancestor of chimpanzees and humans 8 million years ago.

Experiments on imitation typically evaluate a student's ability to copy some feature of an expert's motor behavior. Here, we describe a type of observational learning in which a student copies a cognitive rule rather than a specific motor action. Two rhesus macaques were trained to respond, in a prescribed order, to different sets of photographs that were displayed on a touch-sensitive monitor. Because the position of the photographs varied randomly from trial to trial, sequences could not be learned by motor imitation. Both monkeys learned new sequences more rapidly after observing an expert execute those sequences than when they had to learn new sequences entirely by trial and error.

If POT (parieto-occipital-temporal junction) reorganization came earlier in australopithecines than inHomo, it is likely that the selective pressures were different, and not necessarily directed toward language. The brain endocast evidence for the POT inA. afarensisis actually better than it is for earlyHomo.

It has long been thought that the prefrontal cerebral cortex has been greatly expanded in the human brain. Semendeferi et al. ([2001] Am. J. Phys. Anthropol. 114:224-241) showed that Brodmann's area 10 is relatively larger in the human compared to pongid brains. The question is: how much larger relatively is it? Using their data, it can be shown that the relative increase for human prefrontal area 10 is only 6% larger. Looking at the data base of neural structures provided by Stephan et al. ([1981] Folia Primatol. (Basel) 35:1-29), it is apparent that 6% is a relatively low residual value from a predicted value based on allometric considerations between total brain weight and any given neural structure. When this small increase is combined with their earlier findings on area 13 of prefrontal cortex (Semendeferi et al. [1997] J. Hum. Evol. 32:375-388), it appears that the prefrontal cortex in humans is not some 200% larger as claimed by some researchers (Deacon [1997] Symbolic Species, New York: W.W. Norton; cf. Holloway [1998] Am Sci 86:184-186), and that the findings of Semendeferi et al. ([2001] Am. J. Phys. Anthropol. 114:224-241) are in agreement with the earlier work (Semendeferi and Damasio [2000] J. Hum. Evol. 38:317-332; Semendeferi et al. [1997] J. Hum. Evol. 32:375-388), showing that the human frontal lobe volume is what would be expected for a primate of its brain size. While the prefrontal cortex may have increased relatively in Homo sapiens, the increase is likely to have been far less than currently believed.

Design features for language and stone toolmaking (not tool use) involve similar if not homologous cognitive processes. Both are arbitrary transformations of internal “intrinsic” symbolization, whereas non-human tool using is mostly an iconic transformation. The major discontinuity between humans and non-humans (chimpanzees) is language. The presence of stone tools made to standardized patterns suggests communicative and social control skills that involved language.

Endocasts provide evidence on size and shape characteristics, blood supply trajectories, and neurological features of the brain, allowing comparative analyses of fossil hominins crucial to our understanding of human brain evolution. Here, we assess the morphological features of the virtual endocast of the Cioclovina Upper Paleolithic calvarium, one of the earliest reliably dated European modern human fossils. Our study was conducted on a computed tomography (CT) scan of the original specimen. The endocranial profile was approximated via a semiautomatic segmentation of the CT data. Virtual reconstructions of the endocast were used for assessing the morphological features of the endocranium and for the estimation of the endocranial volume. Cioclovina exhibits a clockwise torque with a small anterior extension of the left frontal lobe over the right one and a protrusion of the right occipital lobe over the left, most likely due to the superior sagittal sinus coursing over the occipital pole. There is an obvious right predominance of the posterior drainage system. Interestingly, the area of the frontal sinus is occupied by dense bony tissue with small air cells corresponding probably to a natural bony loss in the diploe ¨ and to vascular spaces. An estimated endocranial volume of 1498.53 cc was calculated. The convolutional details of the third inferior frontal gyrus (Broca’s caps) are indistinguishable from those found in modern Homo sapiens, and the left occipital lobe appears wider than the right, a possible correlate of right-handedness. Our metric analysis of endocranial measurements also aligns Cioclovina with modern humans. Anat Rec, 294:1083–1092, 2011. V

Despite the ontogenetic allometric size effects that explain much of phyletic variation in brain components, the residuals of some structures indicates that mosaic brain evolution was an important factor in hominid evolution, and that reorganization of the hominid brain may have occurred as early as 3+ MY. Finlay et al.'s allometric technique masks residual variation around allometric trends, and the patterns of residuals relevant to species-specific departures from strict allometric trends.

This report is a description of a reconstructed endocast of the Omo L338y-6 Juvenile Hominid, which has been attributed by Rak and Howell (1978) to the Australopithecus boisei taxon. The reconstructed volume obtained is 427 ml. For a variety of reasons, including the specimen's low endocranial vol- ume, the author regards it more likely that this specimen should be attributed to a gracile line of Australopithecus. In addition to having a low endocranial vol- ume, the cerebellar morphology is more reminiscent of the gracile form, the men- ingeal patterns (as per Saban, 1978) are more indicative of a gracile than robust pattern, and there is no occipital marginal sinus traversing either side of the foramen magnum. The detailed cranial description of the juven- ile L338y-6 hominid from Member E, Shun- gura Formation of the Lower Omo Basin, Eth- iopia, has recently been published by Rak and Howell (1978). In that publication, the au- thors concluded that the specimen was a juven- ile attributable to the Australopithecus boisei taxon. Through the invitation and courtesy of Professor Howell, this author was able to make an accurate endocast mold of that specimen in 1974, and a subsequent reconstruction of the missing frontal and basal portions, to provide a relatively accurate estimation of its cranial capacity. This article is a report of that recon- struction and a discussion of the author's hesi- tation to accept the specimen as an example of the A. boisei taxon.

A restudy of the Danish brain weight data published by Pakkenberg and Voigt ('64), using partial correlation techniques, confirms and extends their earlier conclusions regarding a much stronger allometric relationship between height and brain weight than between body weight and brain weight. The relationship is particularly strong in males, and not in females, which is hypothesized to be related to higher fat components in the latter. Comparative data for smaller samples of Pan, Gorilla, Pongo, Macaca, Papio, and Saimiri using body weights, suggest that such relationships also hold more strongly in males than females, although more reliable data are greatly needed. In addition to providing within-species ranges of variability for variously derived neural statistics (e.g., encephalization quotients, "extra neurons," etc.), for "normal" primates, it is suggested that while allometric trends do exist within species, and particularly males, evolutionary pressures leading to larger brain size were probably very diverse, and that any one homogenistic theory is unlikely.

A quantitative neuropathological necropsy study of 22 control and 22 chronic alcoholic subjects showed a statistically significant loss of brain tissue in the chronic alcoholic group. The loss of tissue appeared to be from the white matter of the cerebral hemispheres rather than the cerebral cortex. This may reflect a primary alteration in the composition or structure of the white matter or it may be secondary to loss of nerve cells from the cortex with subsequent degeneration of the axons in the white matter. Further morphometric analyses including cortical neuronal counts will be necessary to clarify this issue.

Given Wolpoff's (1981) dimensions for lambda-bregma and biparietal breadth, it was possible to reconstruct a new version of the O.H.7 hominid parietals. The constraints of the anatomical features of the original parietal fragments plus Wolpoff's constraints from his own reconstruction, permit testing his claims as a hypothesis. By comparing the resulting distortion of Wolpoff's proposed reconstruction with that of the original reconstruction by Tobias, it is clear that the latter's is far superior to the former's, and that the cranial capacity of O.H.7 of roughly 700 ml is most probable.

New brain endocast reconstructions of Homo erectus discoveries from Indonesia since 1963 (H. erectus VI, 1963; VII, 1965; VIII, 1969) have been made and their volumes determined. In addition, older discoveries (H. erectus I, 1891; 11, 1937; IV, 1937-38) have been reendocast and reconstructed, and have yielded volumes considerably different from those previously published. This is particularly so in the case of Dubois’s original discovery, which yields a volume of 940 ml rather than the widely quoted volume of 750 ml. In addition, a number of morphological observations regarding hemispheric asymmetries (petalias) are provided, which sug- gest a condition similar to modern Homo sapiens. Since 1971, this author has had the oppor- tunity to endocast and provide reconstruc- tions of the Indonesian Homo erectus cranial fragments discovered since 1963 (Jacob, 1966, 1973; Sartono, 1968, 1971). While some preli- minary volumetric determinations have been published elsewhere (Holloway

Latex rubber brain endocasts of solo I, V, VI, X, and XI crania were prepared in order to determine accurate volumes by H2O-displacement and morphological description. The new volumes are not markedly different from previous estimates that had been done by mensuration formulae. The mean volume is 1,151 ml. The endocast surfaces, while devoid of gyral and sulcal relief patterns, do show a preponderance of left-occipital-right-frontal petalia patterns, suggesting right-handedness. Metrical observations support the viewpoint that the solo crania are more closely related to earlier Indonesia homo erectus than to Neandertals.

Earl W. Count. Being and Becoming Human: Essays on the Biogram. New York: Van Nostrand Reinhold Co. Behavioral Science Series, 1973. xv + 349 pp. Tables, bibliography, and index. $14.95 (cloth; $6.95 (paper). Harry J. Jerison. Evolution of the Brain and Intelligence. New York: Academic Press, 1973. xiv + 482 pp. Illustrations, figures, tables, index, and bibliography. $25.00.

Falk's (1980a) claims regarding the pongid-like disposition of convolutional patterns on the South African australopithecine endocasts are critically examined. Using a stereoplotter apparatus and a small sample of chimpanzee brain casts, the angular coordinates of the lunate sulcus are recorded, and placed as such on the Taung and SK 1585 endocasts. The resulting location of such pongid-oriented lunate sulci violates the gross morphology of the australopithecine endocasts. Relative brain: body weight ratios for Australopithecus are shown to be advanced over any of the pongids. In addition, evidence is provided from LeGros Clark's (1947) paper that controverts certain of Falk's claims regarding his methods. It is concluded that the secondary sulci and gyri on the now available australopithecine endocasts are not clear enough to warrant unambiguous demonstration; with regard to the lunate sulcus, the Taung endocast does not show a pongid pattern.

The new SK 1585 endocast, found by Dr. Brain at Swartkrans, 1966, is that of a robust australopithecine, matching the endocast of the Olduvai Hominid 5 in volume, and being almost identical to it in morphology. Aside from Olduvai Hominid 5 it is the only robust australopithecine endocast complete enough to permit easy reconstruction, as only a small portion of the frontal lobe is missing. While the gyral and sulcal patterns are not clear, there are a number of features indicating that the brain is not that of a pongid, but that is has been reorganized to a hominid pattern, particularly the occipital, parietal, and temporal lobes.

A redetermination of endocranial volume of the original 1924 Taung australopithecine described by Dart indicates a volume of 405 cubic centimeters, rather than the 525 cubic centimeters published earlier. The adult volume is estimated to have been 440 cubic centimeters. This value, plus other redeterminations of australopithecine endocasts, lowers the average to 442 cubic centimeters, and increase the likelihood of statistically significant differences from both robust australopithecines and the Olduvai Gorge hominid No. 7.

Full brain endocast reconstructions of the Neanderthals, Spy I and II, Djebel Ihroud I, and the Homo erectus specimen from Sale, Morocco have yielded accurate volumes. Spy I = 1,305 ml; Spy II = 1,553 ml; Djebel ihroud I = 1,305 ml; Sale = 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 Neanderthal 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.