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Journal of Creation 19(1):22–32, April 2005

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Fossil evidence for alleged apemen—Part 1: the genus Homo


This overview analyzes the fossil evidence for the alleged apemen within the genus Homo. The differences in morphological features of the fossil species included in Homo, excluding the invalid taxon Homo habilis, are believed to represent, among other factors, genetic variation within the one human kind. Homo habilis is believed to represent a collection of assorted fossils that either were human (e.g. Homo erectus) or were australopithecine apes. If fossils such as those categorized as Homo erectus and Neandertals were all fully human, then the case for human evolution essentially collapses, as there is an unbridgeable morphological gap between the australopithecine apes and these humans.

In Western society, the educational system and media teach and promote that man is, at best, nothing more than a highly evolved ape, and as their trump card, parade a string of supposed apemen fossils as the knock-out punch to anyone daring to doubt this tale. Is there really convincing fossil evidence proving that man has descended from the apes, or is this just another example of one-sided indoctrination into scientism, a materialistic philosophy that demands natural explanations for all phenomena in the cosmos?1 Put another way; is it possible that the scientists who promote human evolution are not objective in their interpretation of the fossil evidence?

Paleoanthropologist Milford Wolpoff writes: ‘In my view, “objectivity” does not exist in science. Even in the act of gathering data, decisions about what data to record and what to ignore reflect the framework of the scientist.’2 Evolutionists John Gribbin and Jeremy Cherfas acknowledge: ‘… we must admit that the history of palaeontology does not read as a shining example of the pursuit of truth, especially where it was the truth of man’s origins that was at issue’.3 They later say: ‘… we do know that the popular image of the scientist as a dispassionate seeker after the truth could not be further from reality’.4 Lastly, consider the following comment by Roger Lewin, author of the book Bones of Contention: Controversy in the Search for Human Origins:

‘It is, in fact, a common fantasy, promulgated mostly by the scientific profession itself, that in the search for objective truth, data dictate conclusions. If this were the case, then each scientist faced with the same data would necessarily reach the same conclusion. But as we’ve seen earlier and will see again and again, frequently this does not happen. Data are just as often molded to fit preferred conclusions. And the interesting question then becomes “What shapes the preference of an individual or group of researchers?” not “What is the truth?”’5

Scientists, both evolutionist and creationist, tend to interpret what they see in the world through their own peculiar lenses, which represent their framework, worldview or ideology. If the lenses have evolution written on them, then the data will usually be molded to fit that preferred framework. The author believes evolution to be false, and that only through a biblical worldview is our true origin properly understood. According to the Bible, God ‘made of one blood all nations of men’ (Acts 17:26). There is no room for any ‘apemen’ pre-dating humans because ‘from the beginning of the creation God made them male and female’ (Mark 10:6). Therefore, all the supposed apemen belong either to the genus Homo, and are descendants of Adam and Eve, or they belong to extinct apes. The article gives evolutionary ages for the purpose of putting the fossils in an evolutionary context, but in no way implies agreement with these age dates.

Homo habilis (incorporating Homo rudolfensis )

The cranial capacity of Homo habilis ranges from just under 500 cubic centimetres (cm3) to approximately 800 cm3.6 Taxonomic confusion is perhaps the best way to sum up the current status of habilis, as there is considerable debate as to whether the fossils attributed to habilis all belong to the same species. Some experts have split the species into two, creating a new species, Homo rudolfensis, dated from about 1.8 to 2.4 million years ago (Ma), while retaining habilis (dated from about 1.6 to 2.3 Ma), albeit with fewer specimens in the latter.7 To further muddle the picture, Wood and Collard have even suggested that the species rudolfensis (exemplified by cranium KNM-ER 1470) and habilis (exemplified by cranium KNM-ER 1813) be transferred from the genus Homo to Australopithecus,8 but this latter notion has not received wide support. That habilis consists of at least two species is not accepted unanimously, with some evolutionists arguing the variation among specimens of habilis can be explained by intraspecific variation.9

Photo by Raymond Strom4450-fig1
In Western society the idea that man is nothing more than a highly evolved ape is promoted throughout the educational system and media, and the trump card in this propaganda is to parade a string of supposed apemen fossils as a knock-out punch to anyone daring to doubt this tale.

In discussing the multiple species controversy, Wolpoff commented that some scientists had used habilis ‘as a garbage bag’.10 Tattersall and Schwartz have described ‘the status of H. habilis as an all-embracing “wastebasket” species into which a whole heterogeneous variety of fossils could be conveniently swept’.11 Homo habilis is often presented as the evolutionary link between the australopithecines and Homo erectus, but even some evolutionists admit that this notion is too simple. According to Bernard Wood, ‘Advances in techniques for absolute dating and reassessments of the fossils themselves have rendered untenable a simple unilineal model of human evolution, in which Homo habilis succeeded the australopithecines and then evolved via H. erectus into H. sapiens.12 From a creationist position, habilis is an invalid taxon, being instead a collection of assorted fossils that can either be classified as humans (e.g. as erectus) or as australopithecine apes. To illustrate this, some examples are given below.

According to Wolpoff, who labels erectus as early Homo sapiens, the cranium KNM-ER 1813 from Koobi Fora, Kenya ‘is associated with a cranial base and frontofacial region that is so similar to early H. sapiens that authors such as T. White include ER 1813 in the same taxon (for him, this is H. erectus )’.13 Wolpoff describes KNM-ER 1813 as ‘very similar to, really indistinguishable from, early H. sapiens in its teeth and frontofacial architecture (except for its narrow mid-face) but has a much smaller brain size’.14 If the evaluation of KNM-ER 1813 by White and Wolpoff is correct, then this cranium, with a cranial capacity of only about 509 cm3,15 may have belonged to a very small human.

The interpretation of fossil cranium KNM-ER 1470, from Koobi Fora, Kenya, which has a cranial capacity of about 752 cm3,15 has been problematic for both evolutionists and creationists. In 1999 creationist Bill Mehlert’s analysis, which focused on the disputed reconstruction of the face of cranium 1470, led him to believe that the cranium ‘looks increasingly like a larger-brained gracile australopithecine’.16 However, creationist Marvin Lubenow has long argued for its human status, and, in his revised and updated book Bones of Contention, recently stated that ‘comparisons suggest that skull 1470 is more modern than any of the Homo erectus fossils—even the Kow Swamp material, which is only about 10,000 years old’.17 Creationist Malcolm Bowden has also argued that KNM-ER 1470 is ‘simply a small human skull’.18 Although there are variations between specimens KNM-ER 1470 and KNM-ER 1813, much of it can be explained, according to evolutionist Wolpoff, ‘if we assume that the larger crania and faces with powerful postcanine dentitions (and their structural consequences) of specimens such as ER 1470 reflect body size differences’.19 Although a gorilla skull has been found with the same cranial capacity (752 cm3)20 as that of KNM-ER 1470, the cranium of the latter is much more likely that of a human than an ape.

It is not the purpose here to give an exhaustive case-by-case review of the fossils that are categorized as habilis by evolutionists. However, an illustration of a habilis specimen that most likely belongs with the australopithecines (probably africanus) is Stw 53 from Sterkfontein, South Africa.21 Kuman and Clarke list several major morphological traits of Stw 53 that they believe warrant its inclusion in the genus Australopithecus, including teeth that are very large and a braincase that ‘is frontally narrow and restricted’.22 Also, computed tomography (CT) scans of the bony labyrinth of the inner ear have shown that the semicircular canal dimensions in the crania of Stw 53 ‘relied less on bipedal behaviour than the australopithecines’.23 This would seem to rule out human status for this specimen, the incompleteness of which makes an estimate of brain size difficult.24 The labyrinthine morphology study led by Spoor did find that a specimen (SK 847) from Swartkrans, South Africa, associated with habilis, had canal dimensions that were ‘modern-human like’.23 As pointed out by the authors and other researchers,25SK 847 has also been linked to erectus , with Johanson comparing it to erectus specimen KNM-ER 3733.26 Hence, erectus is the most likely status for SK 847, but the cranium is too incomplete to make a definite diagnosis. From the cranial base, Wolpoff has estimated a cranial capacity of less than 500 cm3 for SK 847,27 but given that most of the cranial vault is missing, this estimate is at best a ball park figure.

Postcranially, the modern, human-looking femora KNM-ER 1472 and KNM-ER 1481 are often linked to habilis (or rudolfensis), particularly since they were found in the same Koobi Fora locality as cranium KNM-ER 1470, but as they all come from different sections of the strata, there is no direct association.28 Analysis of The KNM-ER 1481 femur has identified it with erectus,29 and hence indicates it belonged to a human. However, some evolutionists still prefer to refer to it as habilis,30 but this appears to be more in order to prevent the establishment of an erectus presence too early, as the femur is dated by evolutionists to about 2 Ma. Obviously, in this fictitious scenario, the further back in time erectus goes, the less time there is for habilis to evolve into it.

An assortment of fossil crania is illustrated above. The Sangiran and Ngandong specimens are classified as Homo erectus; the Willandra Lakes hominid (WLH-50) and Kow Swamp as modern humans; the Narmada cranium status is unclear because of the uncertainty concerning its ‘evolutionary’ age (usually given as somewhere between 0.15 to 0.6 Ma), but it has been classified as possibly Homo heidelbergensis or archaic Homo sapiens. Studies have shown a closer affinity of the modern human cranium WLH-50 to the Ngandong erectus, than compared to modern human late Pleistocene Africans and Levantines.79 This questions the notion of classifying Homo sapiens and Homo erectus as separate species. (click image for larger view)

The most significant postcranial remains attributed to habilis belong to the partial skeleton OH 62 from Olduvai Gorge, Tanzania, which belonged to an individual that, at the time, was ‘estimated to be as small as or smaller than that of any known fossil hominid’.31 Analyses of limb proportions have indicated a more ape-like humerofemoral index in OH 62 compared to the Lucy skeleton (afarensis), but this result depends on the limb-length estimates being correct.32 Most of the distal half of the OH 62 femur is missing, so its length can only be estimated by comparison to other femurs.33 As illustrated recently by Haeusler and McHenry, using a different femur (OH 34) than the traditional Lucy (AL 288–1) femur that is often used in estimation yielded a humerofemoral index for specimen OH 62 within the modern-human range.34 Hence, as the upper-to-lower limb proportions in OH 62 depend on which femur is used as a model comparison, this measure contributes very little to resolving its taxonomic status. However, the estimated brachial proportion, due to a relatively long forearm, exceeded that of modern humans, being more consistent with that of australopithecines and chimpanzees.35 As pointed out by Lewin, it was the resemblance of the palate from the skull of OH 62 to that of Stw 53 that was influential in assigning OH 62 to habilis.36 As Stw 53 appears to be an australopithecine ape (see above), this may be the most likely status of OH 62 also.

Homo erectus (incorporating Homo ergaster)

Homo habilis is suggested as consisting of fossil specimens that can either be classified as extinct australopithecine apes or as humans, with some of the latter displaying Homo erectus characteristics. The fossils classified as erectus are believed by evolutionists to be the next evolved stage towards modern humans, with habilis the likely ancestor of erectus in this scenario. Using the rule of logic, if fossils attributed to erectus were not those of ‘apemen’, but fully human, then the case for human evolution essentially collapses, as there is an unbridgeable morphological gap between the australopithecine apes and erectus humans, with no missing links in between.

Fossil remains of erectus have been found in many parts of the world, dated by evolutionists from about 1.8 Ma to perhaps less than 100,000 years ago.37 Homo erectus fossils from Java, Indonesia, have been dated to possibly as late as 27,000 years ago, which is quite recent in the evolutionary scheme of things.38 Multiregional evolutionist Wolpoff refers to erectus as early Homo sapiens because ‘no single definition has been found that distinguishes H. sapiens (defined traditionally as the descendant of H. erectus) from H. erectus in all regions where the fossils are found’ and ‘there is no distinct beginning for H. sapiens as long as H. erectus is recognized’.39 Others adopt a multiple species approach, which, in its simplest form, ‘distinguishes early African H. erectus (i.e. fossils mostly from Koobi Fora and West Turkana) as H. ergaster, but leaves other African H. erectus (e.g. OH 9) and the Asian fossils within H. erectus (sensu stricto)’.40 Here, erectus will be considered in the broad sense, including fossils from the restricted definitions of both Homo erectus and Homo ergaster.

A display at the San Diego Museum of Man, shows a replica KNM-ER 1470 cranium shadowed by a couple of ‘apemen’ models.

At an average of about 973 cm3,41 the brain size of erectus is smaller than the average, of about 1,350 cm3,42 for living humans. The cranial capacity range for erectus (727–1,251 cm3) listed by Rightmire43 is in the lower end of the broadest definition of the modern-human range (700–2,200 cm3) given by Molnar.44 However, Molnar gave no source for the lower limit (700 cm3),45 and so the lowest brain size on record for a normal adult is possibly a Melanesian with a cranial capacity of 790 cm3.46

The crania assigned to erectus by Rightmire included Ngandong series, Zhoukoudian series, OH 9, OH 12, Bouri, Trinil, Sangiran series, Dmanisi 2280, KNM-ER 3883, KNM-ER 3733, Buia, Gongwangling, Sale, Hexian, Ceprano and KNM-WT 15000.43 The table of erectus cranial capacities by Rightmire did not include the ‘older subadult or young adult’ Dmanisi cranium D2282 (~650 cm3)47 and the most recent Dmanisi cranium D2700 (~600 cm3),48 the age of which is stated as lying between the juvenile KNM-WT 15000 and D2282.49 Although still not adult, the cranial capacity of these two Dmanisi specimens, assigned to erectus, would not be expected to expand significantly more. The other Dmanisi cranium (D2280) has a measured cranial capacity of 775 cm3.47 However, there is also a lower jaw (D2600), unearthed in 2000, that has been described as ‘enormous’ and ‘far too large to fit comfortably with any of the crania yet discovered’.50 This large variation in size has led to suggestions that more than one species is represented by the Dmanisi fossils (dated by evolutionists to 1.75 Ma), but as the fossils were found in the same stratigraphic layer, it is more likely that they are all members of the same population.51 Stone tools52 found at the Dmanisi site indicate a human presence, and the Dmanisi specimens most likely represent the makers of the tools. That there appears to be a large difference in cranium size within the Dmanisi human population, assuming that the enormous mandible D2600 belonged to a much larger cranium than the others, is consistent with the enormous variation in cranium size that exists in extant humans. A similar, or perhaps larger, degree of size variation than the Dmanisi fossils appears to be present in the Klasies River Mouth human fossils from South Africa (dated from about 0.12 to .09 Ma), regarded by evolutionists as ‘near modern’, as indicated by variation in lower jaw sizes, with one mandible (KRM 16424) described by Klein as ‘among the smallest adult human jaws ever recorded’.53

Brain size and intelligence

Does the difference in size, per se, between the average modern-human brain and the average erectus brain support the evolutionary notion that the brain has evolved in size during the alleged period of hominid evolution? The answer is no! According to evolutionist Holloway:

‘The range of variation of cranial capacity of modern Homo sapiens is about 1,000 c.c., with no correlation between capacity and behavior readily demonstrable. Such a figure represents almost the total amount of increase in capacity from the Australopithecine level to that of modern man.’54

Physical anthropologist John Relethford acknowledges that ‘Although their brain size was somewhat smaller than ours today, Homo erectus had an essentially human skeleton from the neck down, made sophisticated stone tools, and possibly used fire.’55 The ability to make sophisticated stone tools indicates that a smaller brain size was no barrier to erectus possessing human intelligence. It should be remembered that Anatole France, who had a brain size of about 1,000 cm3, only fractionally above the erectus average, won the 1921 Nobel Prize for Literature.56 Hence, why would evolution (if it could) bother developing a larger brain, at great cost, when it would provide no obvious extra benefit to that of a smaller brain? Evolution is supposedly all about adaptive value of new novelties (a minute few of which may confer some benefit) that are believed to be randomly generated by freakishly improbable genetic mutations. Hence, if a larger brain has no apparent adaptive value, then clearly it could not evolve even if evolution was possible. It has not been demonstrated how even ‘beneficial’ genetic changes can increase the functional information content of the genome, as these DNA changes generally involve only sorting and loss of information.57 Hence, the mechanism for ‘upward’ evolutionary change is a mysterious ‘black box’. The brain is almost infinitely complex, and to believe that some unknown natural force has been driving it to ever-increasing size during the period of alleged human evolution, without even any plausible adaptive value, is to believe in zero probability. Something else must have happened to explain the incredible variation in brain size of humans, and this was intelligent design by a Creator. The following quote by Holloway illustrates the dilemma for the evolutionist:

‘For another, there is some difficulty in suggesting that natural selection kept favoring larger brains if there is no connection made between the neural structures of the cortex and increasing behavioral adaptation. That is, the very units which comprise the gradual increase in cranial capacity over the span of the Pleistocene, cubic centimeters, cannot be demonstrably linked with real differences in behavior. The modern condition, where there is almost 1,000 c.c. variation without behavioral difference that can be analysed, warns that in attempting to explain the increase in cranial capacity during hominid evolution, some other parameter(s) must be used.’58
Louis Leakey found the Homo erectus cranium OH 9 in 1960 at Olduvai Gorge, Tanzania. It is dated to 1.2 Ma and has a cranial capacity of 1067 cm3. It has huge brow-ridges. CT scans of the bony labryrinth of the inner ear of this specimen indicate a modern human morphology, reflecting human locomotion. The photo was taken at the San Diego Museum of Man.

This has not stopped a plethora of evolutionary ‘just-so-stories’ on how we supposedly evolved a large human brain, culminating with the ultimate absurdity that our ‘enormous human brain has been created by the memes’.59 However, some may question whether the smallest erectus specimens had brains capable of human intelligence. If the recent fossil finds classified as Homo floresiensis (more later) are a guide, then the answer has to be in the affirmative as, in the words of evolutionist Kate Wong, ‘Would anyone have guessed that a creature with a skull the size of a grapefruit might have possessed cognitive abilities comparable to those of anatomically modern humans?’60 According to erectus expert Philip Rightmire of Birmingham University: ‘If Homo floresiensis was capable of producing sophisticated tools, we have to say that brain size doesn’t add up to much.’56 It should be remembered, as stated by Holloway, that ‘One c.c. of chimpanzee cortex is not equivalent to one c.c. of human cortex, nor is it likely that any equivalent measure can be found.’61 Hence, it appears that neural organization is far more important than brain size, per se. Also, as discussed above, there is no demonstrable correlation between cranial capacity and behaviour, including measures of intelligence, as indicated by the following statement by Clark :

‘So far as it has been possible to apply appropriate tests, there is within such limits no marked correlation between the brain size and intelligence. To the paleo­anthropologist this lack of correlation is particularly disconcerting for it means that he has no sure method of assessing the mental capacity of extinct types of hominid simply by reference to cranial capacity.’62

Locomotion and postcranial skeleton

CT scans of the bony labyrinth of the inner ear, in the few erectus specimens examined (OH 9, Sangiran 2 and 4), have indicated a modern-human morphology, reflecting human locomotion.63 As already mentioned, evolutionists acknowledge that the postcranial skeleton of erectus was essentially human.55 The first erectus postcranial skeleton of any significance (KNM-ER 1808) was discovered in 1973, dated at 1.7 Ma, but because of a bone disease, hypervitaminosis A, it was useless in terms of giving a clear picture of normal erectus morphology.64 The skeleton of the female KNM-ER 1808 was estimated to be 173 cm tall,65 and at the time the erectus postcranial skeleton was represented more by KNM-ER 1808 than all previous erectus postcrania combined.66

Most of the information about the postcranial anatomy of erectus comes from the later discovery, at west Lake Turkana, Kenya, in 1984, of the almost complete skeleton of the 1.68-metre-tall Nariokotome boy (KNM-WT 15000), dated at 1.6 Ma.67 The skeleton is also known as the Turkana boy, and is classified as Homo ergaster by the ‘splitters’. The skull morphology of the Nariokotome boy was erectus-like, but Wolpoff describes the postcranium of this individual as ‘mostly modern’.68 The limb proportions of KNM-WT 15000, specifically the humerofemoral and brachial index, resembled modern humans.69 According to Lewin the information gathered from the Nariokotome boy skeleton indicates that the erectus postcranium ‘is similar to that of modern humans, but more robust and heavily muscled’, which ‘implies routine heavy physical exertion’.70 The cranial capacity of the boy, estimated to be 11 years old, measured about 880 cm3 at the time of his death, and an estimate of adult brain size is 909 cm3.71 As pointed out by Mehlert, there is no way to establish adult height size with certainty,72 but 185 cm is one estimate given for KNM-WT 15000.65

To have such a tall erectus individual with a modern postcranium appear at such an early stage in the alleged evolutionary history of erectus is a problem for evolutionists. If evolution was true, then a more intermediate postcranial skeleton would be expected, one reflecting more of a mid-way stage between the australopithecines and modern humans, not one already at the modern human stage. Hence, there is a huge morphological gap between erectus and the australopithecines; the habilis taxon, as discussed earlier, is regarded as invalid. In what seems an almost desperate effort to dehumanize the Nariokotome boy, some evolutionists emphasize that the vertebral canal in this individual was smaller than in modern humans.73 As such, they argue that his nervous system was not developed enough to carry out the entire fine breathing manoeuvres required for a fully human discourse, and conclude that at the time the boy lived ‘Language, as we understand the term, had probably not yet fully evolved.’74 However, the revelation that the KNM-WT 15000 axial skeleton had significant abnormalities, suggesting that there was some form of abnormal development in the axial skeleton of the Nariokotome boy, nullifies any such argument and it can explain the narrowness of the vertebral canal.75 This verdict, however, is still not accepted by some evolutionists.76

Skull features

The Broken Hill cranium from Kabwe, Zambia is classified by most evolutionists as belonging to Homo heidelbergensis. The photo was taken at the San Diego Museum of Man.

Skulls classified as erectus are considered by evolutionists to exhibit key characteristics that differentiate them from modern humans. Key characteristics include: prominent browridges; insignificant chin; large mandible; forwardly projecting jaws; a flat, receding forehead; a long and low-vaulted cranium; occipital torus; relatively large teeth; relatively large facial skeleton; and a thick-walled braincase.77 A major problem for evolutionists is that many (if not all) of the above-mentioned features, which supposedly differentiate erectus from modern humans, also occur in modern humans. This is illustrated in recent native Australians by the prominent browridges of cranium 3596 from Euston,78 and the closer affinity of the modern human cranium from Australia, WLH-50, with the Ngandong erectus, compared to modern human late Pleistocene Africans and Levantines.79 According to Shreeve,

‘While some of the early modern humans from Australia look much like people today, others bear all the markings of a more robust kind of human, with thick skull bones, swollen browridges, and huge teeth, even bigger than those of Homo erectus in some specimens.’80

Examples of other typical erectus-type features in modern humans, such as flattish receding forehead and insignificant chin development, can be seen in a photograph of a living native Australian, published in the late Victorian age, when there was appalling racism within anthropology.81 Native Australians are as human and ‘modern’ as anyone else, and so the above erectus-type features cannot be considered ‘primitive’.

Stringer and Gamble, advocates of the Out of Africa theory of modern human origins, referred to the presence of the erectus-type features in Australian Aborigines as perhaps ‘apparent evolutionary reversals’,82 triggering a heated response from a group stating ‘such statements and their implications are unfortunate’.83 Controversy aside, the statement does illustrate the chameleon-like nature of evolution theory, which appears plastic enough to accommodate almost any scenario. Clearly, there is no valid basis for rejecting erectus fossils as being fully human because of skull features that some evolutionists regard as being ‘primitive’ characters. Creationists are not the only ones protesting about the narrow definition of our species. In regards to the Out of Africa theory of modern human origins, evolutionists from the multiregional school of thought have expressed the following concern about defining the species Homo sapiens too restrictively:

‘We believe that an unfortunate aspect of the debate are [sic] definitions of Homo sapiens used by some “Eve” theorists. They have been found to exclude many Pleistocene and more recent Aboriginal Australians from our species (Wolpoff, 1986; P. Brown, 1990). Further examination of these individuals and collections of recent Aboriginal skeletal remains leads us to estimate that these definitions of modern Homo sapiens exclude anywhere between 40 000 and 60 000 living Aboriginal Australians. We feel that there is great danger in this. It is the duty of specialists to make sure that they include all living people in any definition of our species. If we do define humans as minimally including all living people, many of the fossils that the “Eve” theorists claim leave no descendants, including Neanderthals, fall into Homo sapiens.’84
Photo by David Green4450-nea
The Neandertal Gibraltar 1 cranium was found in Forbes’ Quarry, Gibraltar prior to 1848, and is dated somewhere between 45,000 and 70,000 years ago. It is said to be the first adult Neandertal cranium discovered, but was not recognized as such until after the discovery of the original Neandertal fossils in the Feldhofer cave, Germany in 1856.

For the purpose of analysis, erectus has been considered as a separate group, but is it really that different from other fossil humans? For example, are fossil specimens allocated to erectus just because of their skull morphology, or is there a trend of categorizing specimens with smaller cranial capacities as erectus, and larger specimens to other taxa, such as Homo heidelbergensis and Neandertals? As the discussion moves on to the next group of fossil humans, the following comment from evolutionist Harry Shapiro is very revealing:

‘But when one examines a classic Neanderthal skull, of which there are now a large number, one cannot escape the conviction that its fundamental anatomical formation is an enlarged and developed version of the Homo erectus skull. As in Homo erectus, it has the bun-shaped protrusion in the occiput, the heavy brow ridge, the relatively flattened crown that from the rear presents a profile like a gambrel roof. Its greatest breadth is low, just above the ears, and the absence of a jutting chin is typical.’85

Homo heidelbergensis (archaic Homo sapiens)

Homo heidelbergensis is a category invented to fill the alleged taxonomic vacuum between the Neandertals and erectus. Previously, these fossils were labelled as archaic Homo sapiens.86 Evolutionist Shreeve has referred to the taxon as ‘more like a bushel basket into which you throw everything that is neither clearly erectus, nor obviously modern Homo sapiens’.87 The heidelbergensis braincases are described as being ‘more robustly built’ than those of modern humans, and to ‘have some, but not all, of the features of H. erectus crania, but lack the derived features of Neanderthal crania’.88 The validity of having separate species classifications for erectus and heidelbergensis is questionable when, for example, the erectus Ngandong series crania43 have also been classified as archaic Homo sapiens (i.e. heidelbergensis),89 and some evolutionists even advocate including the Ngandong fossils within Homo sapiens.90 With crania displaying such interchangeability up and down the ranks of the genus Homo, evolutionists can hardly complain about creationists lumping the above species together. The cranial capacity range of heidelbergensis is between 1,100 and 1,390 cm3 (mean of about 1,206 cm3), with age dates varying between 200,000 and 700,000 years ago.91 The cast of specimens assigned to heidelbergensis includes Dali, Broken Hill, Bodo, Arago, Jinniushan, Ndutu, Petralona, Steinheim and Sima de los Huesos 4 and 5.92 The arguments above for assigning human status to erectus apply equally to heidelbergensis, particularly as evolutionists regard them as more ‘modern’ than erectus.

Homo antecessor

The tendency to split the genus Homo into more and more species is revealed by naming the fragmentary Gran Dolina remains from Spain, which included a juvenile partial face (ATD6-69) that had a ‘fully modern facial topography’,93 as a new species, Homo antecessor. Surely room could have been found in the heidelbergensis ‘bushel basket’ to include the Grand Dolina remains. One suspects, with an evolutionary age (about 0.78 Ma) of the remains that was older than any member of heidelbergensis from Europe, the temptation to give these ‘oldest known Europeans’ a new name was just too much at the time, particularly as antecessor then ‘claims a key spot on the human family tree’.94

Homo neanderthalensis (Neandertal)

Neandertals are believed by evolutionists to have been confined to Europe, western Asia and the Middle East between about 30,000 and 150,000 years ago, and are regarded by most evolutionists ‘as a side branch of the human evolutionary tree, with extinction their fate’.95 The relatively long history of the discovery and emerging knowledge of the Neandertals has been told many times, albeit mostly from an evolutionary point of view, and will not be revisited here.96 The Neandertals had quite a culture inventory, and buried their dead.97 To anyone not blinded by evolutionary bias, this in itself should be ample evidence that the Neandertals were fully human. Classical Neandertal specimens include Neandertal, La Chapelle-aux-Saints, La Ferrassie I, Spy I, Le Moustier, Saccopastore II, Shanidar 1 and 5, Tabun and La Quina, while ‘progressive’ specimens include Spy II, Saccopastore I, Monte Circeo, the Krapina remains, Shanidar 2 and some of the Skuhl and Qafzeh specimens.98 The Neandertals labelled ‘classical’ are considered by some evolutionists to be the more ‘primitive’.99

The mean Neandertal brain size of about 1,485 cm3 (range: 1,245–1,740 cm3)100 is at the very least on par with modern humans, if not slightly larger. Apart from a large cranial capacity, Lubenow lists the following distinct Neandertal morphology:

‘(2) skull shape low, broad, and elongated; (3) rear of the skull rather pointed, with a bun; (4) large, heavy browridges; (5) low forehead; (6) large, long faces with the center of the face jutting forward; (7) weak, rounded chin; and (8) postcranial skeleton rugged with bones very thick.’101

Other adult Neandertal features include a retromolar space, broad nasal opening and large dentition.102 While evolutionists regard Neandertal as a separate species, a creationist view is that ‘erectus is just a smaller version of Neandertal and the most unique aspect of both is their skull shape’.103 There are also non-evolutionary explanations for some of the Neandertal features, such as the stress of biomechanical forces influencing skull morphology.104 Additionally, in his book Buried Alive, Jack Cuozzo demonstrates disturbing instances of faulty reconstructions of Neandertal specimens. In one example he illustrates how the Le Moustier specimen has been assembled to make the jaw appear more ape-like than it was,105 and in another, Cuozzo presents evidence that the chin of La Quina 5 was cut off to make it appear more ape-like.106

As mentioned previously, many of the features supposedly differentiating erectus and Neandertal from modern humans also occur in some modern humans. For this reason the proponents of the multiregional view of human evolution, in contrast to those of the Out of Africa view, believe that Homo erectus, archaic Homo sapiens (heidelbergensis) and Neandertals ‘should be reclassified into a single species, Homo sapiens, that is subdivided only into races’, because they are insufficiently distinct from Homo sapiens.107 Consider the following statement by proponents of the multiregional school:

‘Neandertals have much larger browridges than living Europeans, and they are always continuously developed across the forehead. A significant number of recent and living Indigenous Aboriginal Australians have large, continuously developed browridges. Does this make them more primitive than Europeans? Does this make the Neandertals modern?’108

If you believe that certain skull traits are indicative of a more ‘primitive’ status, then the above questions pose a real problem.

According to Stringer and Gamble,
‘The Neandertals were not apemen, nor missing links—they were as human as us, but they represented a different brand of humanity, one with a distinctive blend of primitive and advanced characteristics.’109

This seems at best a confusing statement, as how can one say the Neandertals were ‘as human as us’, and then immediately follow this by a qualifier that ‘they represented a different brand of humanity’? Either they were human or they were not. As aptly put by Lubenow, ‘The Neandertal problem is primarily the evolutionists’ problem. Simply put, evolutionists don’t know where the Neandertals came from or where they went.’110 To creationists, Neandertals were fully human. There is no basis for considering some skull features as more primitive than others because we are all equally human, regardless of the diversity of features that exists within the human kind, and because there never were any apemen.

Homo floresiensis

Media headlines in late October 2004, such as ‘Lost race of human “hobbits” unearthed on Indonesian island’,111 must have astonished every ‘hominid’ watcher on the planet. For once, the incredible media ‘hoopla’ surrounding the announcement of yet another supposed new hominid species, Homo floresiensis, was not overrated, although the assignment of a new species name to these hobbits seems a bit premature, as, despite their small size, the remains may well be descendants of Adam.112 The hobbits must have had substantial seafaring skills to reach Flores and sophisticated cognitive abilities, ‘as indicated by the technology of the stone artifacts associated with H. floresiensis at Liang Bua’.113 If the tools belonged to floresiensis, which seems very likely, then these people clearly possessed human intelligence.

The finding of fossils from hobbit-size people, who appear to have possessed human intelligence, with one specimen (LB1) evolutionarily dated to around 18,000 years ago and standing about 1 metre tall, with a cranial capacity of approximately 380 cm3,114 questions the notion of an arbitrary cerebral rubicon (at least at the 600–800 cm3 brain size level)115 that must be passed in order to have a human mental faculty. People with microcephalic brains (400–600 cm3),116 as well as dwarf humans (517 cm3),117 also have brain sizes measured below this arbitrary rubicon. The average brain size of chimpanzees is 383 cm3, orangutans, 404 cm3, and gorillas, 504 cm3.42 Hence, the 380 cm3 brain size of floresiensis from the Indonesian island of Flores is very small if it is human. However, when considering brain size, one should also take into account body size. This is done when calculating a value known as the encephalization quotient (EQ).118 If the body of floresiensis specimen LB1 is assumed lean and narrow, then the estimated EQ places LB1 easily within the erectus range.119

In terms of similarity, LB1 is described as: ‘In the overall shape of its skull and its teeth, the creature most closely resembles Homo erectus.’120 Despite its small stature and cranial capacity, LB1 had few other things in common with the australopithecines. According to the authors of the floresiensis paper:

‘… it does not have the great postcanine tooth size, deep and prognathic facial skeleton, and masticatory adaptations common to members of this genus. Instead, the facial and dental proportions, postcranial anatomy consistent with human-like obligate bipedalism, and a masticatory apparatus most similar in relative size and function to modern humans all support assignment to the genus Homo —as does the inferred phylogenetic history, which includes endemic dwarfing of H. erectus.’121

Peter Brown, paleoanthropologist and first author of the floresiensis Nature paper, in regards to the hobbit’s small cranium, commented that ‘The internal structure of the brain—the neural pathways—must have been more human-like than ape-like to be able to make these types of tools.’122 An even more likely scenario is that the internal structure of floresiensis’ brain was human, as was the brain architecture of many other fossil specimens with small craniums, in particular those assigned to erectus.

The team who unearthed the find suggests that floresiensis may be the descendants of erectus from the nearby island of Java, believed to have been there as long as 1.6 Ma.123 They comment that the first hominid immigrants to Flores ‘may have had a similar body size to H. erectus and early Homo, with subsequent dwarfing; or, an unknown small-bodied and small-brained hominin may have arrived on Flores from the Sunda Shelf’.119 An alternative view is that floresiensis is ‘a miniature human being exhibiting part of the same range of post-Babel human variation as encompasses the larger so-called Homo erectus’.124 Claims have been made by pathologist Maciej Henneberg of the University of Adelaide that the LB1 individual suffered from a pathological growth condition called secondary microcephaly, and that ‘the skull of the Flores hominid is very similar to a 4,000-year-old microcephalic modern human skull found on the island of Crete’.125 Also, Indonesian paleoanthropologist Teuku Jacob is reported to have said the LB1 skeletal remains were from a ‘modern human, Homo sapiens, that lived about 1,300 to 1,800 years ago’ who was a member of the ‘Australomelanesid race, which had dwelled across almost all of the Indonesian islands’,124 and that the Flores people suffered ‘from microcephaly which shrank their brains to the size of a chimpanzee’s’.126 However, the more remains of these tiny individuals that are found, the stronger the argument against LB1 being a diseased individual is, and there are reports of another lower jaw identical in shape and size to LB1’s.56

The controversy over the hobbit may well result in two rival camps feuding over the issue, a bit like the ongoing quarrel between the Out of Africa and multiregional schools of thought over the origin of modern humans. If so, don’t expect any resolution soon. However, even if the specimens turn out to be pathological, the use of sophisticated tools, even by ‘abnormal’ people, indicates that they were quite intelligent, and illustrates that brain size, per se, is not as important as neural organization.


Homo habilis consists of fossil specimens that can either be classified as extinct australopithecine apes or as humans, with some of the latter displaying Homo erectus characteristics. Without the burden of having to fit fossils into an evolutionary scheme, there is no reason not to accept fossils such as those categorized as erectus, and Neandertals as belonging to the one human kind. Differences in skeletal anatomy may simply reflect a greater genetic diversity within the human kind in the past, and in some instances living under particularly harsh environmental conditions, or even dietary habits, may have influenced skeletal development. The stress of peculiar biomechanical forces, as well as pathology,127 may also have influenced skull and postcranial morphology in some instances. The Bible also indicates that people lived longer in the past, with longevity declining post-Flood. As most of the fossils would have belonged to early post-Flood humans, it is possible that their natural lifespans may have been greater than those of people today. Hence, it is unclear what effect longevity, and possibly a different rate of skeletal maturation, would have had on skeletal features.

Posted on homepage: 29 June 2006


  1. Shermer, M., The shamans of scientism, Scientific American 286(6):25, 2002. Return to text.
  2. Wolpoff, M.H., Paleoanthropology, Second Edition, McGraw-Hill, Boston, p. iv, 1999. Return to text.
  3. Gribbin, J. and Cherfas, J., The First Chimpanzee: In Search of Human Origins, Penguin Books, London, p. 59, 2001. Return to text.
  4. Gribbin and Cherfas, ref. 3, p. 148. Return to text.
  5. Lewin, R., Bones of Contention: Controversies in the Search for Human Origins, Penguin Books, London, p. 68, 1987. Return to text.
  6. Wood, B. and Richmond, B.G., Human evolution: taxonomy and paleobiology, J. Anatomy 196:39, 2000. Return to text.
  7. Wood, B. and Collard, M., The human genus, Science 284:66, 1999. Return to text.
  8. Wood, B. and Collard, M., The changing face of genus Homo, Evolutionary Anthropology 8:204, 1999. Return to text.
  9. Miller, J.M.A., Craniofacial variation in Homo habilis: an analysis of the evidence for multiple species, American J. Physical Anthropology 112:103–128, 2000. Return to text.
  10. Wolpoff, ref. 2, p. 358. Return to text.
  11. Tattersall, I. and Schwartz, J.H., Extinct Humans, Westview Press, New York, p. 111, 2001. Return to text.
  12. Wood, B., Origin and evolution of the genus Homo, Nature 355:783, 1992. Return to text.
  13. Wolpoff, ref. 2, pp. 369–370. Return to text.
  14. Wolpoff, ref. 2, p. 373. Return to text.
  15. Holloway, R.L., Problems of brain endocast interpretation and African hominid evolution; in: Jolly, C.J. (Ed.), Early Hominids of Africa, Duckworth, London, p. 387, 1978. Return to text.
  16. Mehlert, A.W., The rise and fall of skull KNM-ER 1470, Journal of Creation 13(2):100, 1999; creation.com/knmer1470. Return to text.
  17. Lubenow, M.L., Bones of Contention: A Creationist Assessment of Human Fossils, Revised and Updated, Baker Books, Grand Rapids, MI, p. 328, 2004. Return to text.
  18. Bowden, M., Apemen: Fact or Fallacy?, Second Enlarged Edition, Sovereign Publications, Bromley, Kent , p. 200, 1981. Return to text.
  19. Wolpoff, ref. 2, p. 387. Return to text.
  20. Holloway, R.L., Cranial capacity, neural reorganization, and hominid evolution: a search for more suitable parameters, American Anthropologist 68:113, 1966. Return to text.
  21. Berger, L.R. and Hilton-Barber, B., In the Footsteps of Eve: The Mystery of Human Origins, Adventure Press, National Geographic, Washington, D.C., pp. 239–240, 2000. Return to text.
  22. Kuman, K. and Clarke, R.J., Stratigraphy, artefact industries and hominid associations for Sterkfontein, Member 5, J. Human Evolution 38:841, 2000. Return to text.
  23. Spoor, F., Wood, B. and Zonneveld, F., Implications of early hominid labyrinthine morphology for evolution of human bipedal locomotion, Nature 369:648, 1994. Return to text.
  24. Tattersall and Schwartz, ref. 11, p. 113. Return to text.
  25. Tattersall and Schwartz, ref. 11, p. 112; Wolpoff, ref. 2, pp. 383–384. . Return to text.
  26. Johanson, D. and Edgar, B., From Lucy to Language, Simon & Schuster Editions, New York , p.184, 1996. Return to text.
  27. Wolpoff, ref. 2, p. 384. Return to text.
  28. Leakey, R.E.F., Evidence for an advanced Plio-Pleistocene hominid from East Rudolf, Kenya, Nature 242:447–450, 1973. Return to text.
  29. Kennedy, G.E., A morphometric and taxonomic assessment of a hominine femur from the lower member, Koobi Fora, Lake Turkana, American J. Physical Anthropology 61:433, 1983. Return to text.
  30. Trinkaus, E., Does KNM-ER 1481A establish Homo erectus at 2.0 myr BP? American J. Physical Anthropology 64:137–139, 1984. Return to text.
  31. Johanson, D.C. et al, New partial skeleton of Homo habilis from Olduvai Gorge, Tanzania, Nature 327:208, 1987. Return to text.
  32. Richmond, B.G., Aiello, L.C. and Wood, B.A., Early hominin limb proportions, J. Human Evolution 43:530–531, 2002. Return to text.
  33. Haeusler, M. and McHenry, H.M., Body proportions of Homo habilis reviewed, J. Human Evolution 46:433–437, 2004. Return to text.
  34. Haeusler and McHenry, ref. 33, p. 461. Return to text.
  35. Haeusler and McHenry, ref. 33, p. 460. Return to text.
  36. Lewin, R., Human Evolution: An Illustrated Introduction, Fifth Edition, Blackwell Publishing, Malden, MA, p. 141, 2005. Return to text.
  37. Anton, S.C., Natural history of Homo erectus, Yearbook of Physical Anthropology 46:128–132 (Supplement S37 to the American J. Physical Anthropology, Vol. 122), 2003. Return to text.
  38. Swisher, C.C. III, Rink, W.J., Anton, S.C., Schwarcz, H.P., Curtis, G.H., Suprijo, A. and Widiasmoro, et al., Latest Homo erectus of Java: potential contemporaneity with Homo sapiens in Southeast Asia, Science 274:1870–1874, 1996. Return to text.
  39. Wolpoff, ref. 2, pp. 396–397. Return to text.
  40. Anton, ref. 37, p. 154. Return to text.
  41. Rightmire, G.P., Brain size and encephalization in Early to Mid-Pleistocene Homo, American J. Physical Anthropology 124:113, 2004. Return to text.
  42. Tobias, P.V., Evolution of the human brain; in: Gordon, E. (Ed.), Integrative Neuroscience, Harwood Academic Publishers, Amsterdam, p. 39, 2000. Return to text.
  43. Rightmire, ref. 41, p. 110. Return to text.
  44. Molnar, S., Races, Types, and Ethnic Groups, Prentice-Hall Inc., NJ, p. 57, 1975. Return to text.
  45. Foley, J., Creationist arguments: brain sizes, www.talkorigins.org/faqs/homs/a_brains.html, 17 November 2004. Return to text.
  46. Jue, D.S., Cranial capacity and endocranial casts, Journal of Creation 4:56, 1990; creation.com/cranial-capacity-and-endocranial-casts. Return to text.
  47. Gabunia, L. et al., Earliest Pleistocene hominid cranial remains from Dmanisi, Republic of Georgia : taxonomy, geological setting and age, Science 288 :1019, 2000. Return to text.
  48. Vekua, A. et al., A new skull of early Homo from Dmanisi, Georgia, Science 297:88, 2002. Return to text.
  49. Vekua, ref. 48, p. 86. Return to text.
  50. Wong, K., Stranger in a New Land, Scientific American 289(5):56, 2003. Return to text.
  51. Wong, ref. 50, p. 59. Return to text.
  52. Gabuna, L., Anton, S.C., Lordkipanidze, D., Vekua, A., Justus, A. and Swisher III, C.C., Dmanisi and dispersal, Evolutionary Anthropology 10:164, 2001. Return to text.
  53. Klein, R.K. and Edgar, B., The Dawn of Human Culture, John Wiley & Sons Inc., New York, pp. 227–229, 2002. Return to text.
  54. Holloway, ref. 20, p. 103. Return to text.
  55. Relethford, J.H., Reflections of Our Past: How Human History is Revealed in our Genes, Westview Press, Boulder, CO, p. 46, 2003. Return to text.
  56. Wong, K., The littlest human, Scientific American 292(2):48, 2005. Return to text.
  57. Sarfati, J., Refuting Evolution 2, Master Books, Green Forest, AR, pp. 56, 101–108, 2002. Return to text.
  58. Holloway, ref. 20, p. 115. Return to text.
  59. Blackmore, S., The Meme Machine, Oxford University Press, Oxford, p. 81, 1999; For a critical review of this book, see: Line, P., Unleashing the meme: is this the end of our existence? Creation Matters 7(2), 2002. Return to text.
  60. Wong, ref. 56, p. 42. Return to text.
  61. Holloway, ref. 20, p. 108. Return to text.
  62. Clark, W.E. LeGros, Bone of contention; in: Korn, N. and Thompson, F.W. (Eds.), Readings in Physical Anthropology, Holt, Reinehart and Winston Inc., New York; as quoted in: Jue, ref. 46, p. 57. Return to text.
  63. Spoor et al., ref. 23, pp. 645–648. Return to text.
  64. Walker, A. and Shipman, P., The Wisdom of Bones: In Search of Human Origins, Phoenix, London, pp. 128–134, 1996. Return to text.
  65. Wolpoff, ref. 2, p. 408. Return to text.
  66. Walker and Shipman, ref. 64, p. 157. Return to text.
  67. Brown, F., Harris, J., Leakey, R. and Walker, A., Early Homo erectus skeleton from west Lake Turkana, Kenya, Nature 316:788, 1985. Return to text.
  68. Wolpoff, ref. 2, pp. 402–403. Return to text.
  69. Richmond et al., ref. 32, pp. 534–542. Return to text.
  70. Lewin, ref. 36, p. 163. Return to text.
  71. Walker and Shipman, ref. 64, p. 184. Return to text.
  72. Mehlert, A.W., Homo erectus ‘to’ modern man: evolution or human variability? Journal of Creation 8(1):107, 1994; creation.com/homo-erectus-to-modern-man-evolution-or-human-variability. Return to text.
  73. MacLarnon, A. and Hewitt, G., Increased breathing control: another factor in the evolution of human language, Evolutionary Anthropology 13:186–187, 2004. Return to text.
  74. Stringer, C. and McKie, R., African Exodus: The Origins of Modern Humanity, Jonathan Cape, London, p. 30, 1996. Return to text.
  75. Latimer, B. and Ohman, J.C., Axial dysplasia in Homo erectus, J. Human Evolution 40:A12, 2001. Return to text.
  76. MacLarnon and Hewitt, ref. 73, pp. 194–195. Return to text.
  77. Lubenow, ref. 17, p. 122; Lewin, ref. 36, p. 163; Klein, R.G., The Human Career, Second Edition, The University of Chicago Press, Chicago, pp. 283–289, 1999. Return to text.
  78. Hawks, J., Oh, S., Hunley, K., Dobson, S., Cabana, G., Dayalu, P. and Wolpoff, M.H., An Australian test of the recent African origin theory using the WLH-50 calvarium, J. Human Evolution, 39:17, 2000. Return to text.
  79. Hawks et al., ref. 78, pp. 1–22; Wolpoff, M.H., Hawks, J., Frayer, D.W. and Hunley, K., Modern human ancestry at the peripheries: a test of the replacement theory, Science 291:293–297, 2001. Return to text.
  80. Shreeve, J., The Neandertal Enigma, William Morrow and Company Inc., New York, p. 100, 1995. Return to text.
  81. Hutchinson, H.N., Gregory, J.W. and Lydekker, R., The Living Races of Mankind, Hazell, Watson and Viney Ltd., London, pp. 60, Undated, but late Victorian. . Return to text.
  82. Stringer, C.B. and Andrews, P., Genetic and fossil evidence for the origin of modern humans, Science 239 :1267, 1988. Return to text.
  83. Wolpoff, M.H., Spuhler, J.N., Smith, F.H., Radowcic, J., Pope, G., Frayer, D.W., Eckhardt, R. and Clarke, G., Modern human origins, Science 241:772, 1988; see also: Shreeve, ref. 80, p. 109. Return to text.
  84. Thorne, A. and Wolpoff, M., Conflict over modern human origins, Search 22(5):177, 1991. Return to text.
  85. Shapiro, H.L., Peking Man, George Allen & Unwin Ltd, London, p. 125, 1974. Return to text.
  86. Wood and Collard, ref. 8, p. 197; Lubenow, ref. 17, p. 199. Return to text.
  87. Shreeve, ref. 80, p. 82. Return to text.
  88. Wood and Collard, ref. 8, p. 197. Return to text.
  89. Brauer, G. and Mbua, E., Homo erectus features used in cladistics and their variability in Asian and African hominids, J. Human Evolution 22:82, 1992. Return to text.
  90. Hawks et al., ref. 78, p. 21. Return to text.
  91. Rightmire, ref. 41, pp. 112–115. Return to text.
  92. Rightmire, ref. 41, p. 112. Return to text.
  93. Bermudez de Castro, J.M., Arsuaga, J.L., Carbonell, E., Rosas, A., Martinez, I. and Mosquera, M., A hominid from the lower Pleistocene of Atapuerca, Spain: possible ancestor to Neandertals and modern humans, Science 276:1392, 1997. Return to text.
  94. Gibbons, A., A new face for human ancestors, Science 276:1331, 1997. Return to text.
  95. Lewin, ref. 36, pp. 179, 185. Return to text.
  96. See, for example: Tattersall, I., The Last Neanderthal: The Rise, Success, and Mysterious Extinction of Our Closest Human Relatives, Macmillan, New York , pp. 74–119, 1995. Return to text.
  97. Lubenow, ref. 17, pp. 236–257. Return to text.
  98. Beasley, G.J., A possible creationist interpretation of archaic fossil human remains, Journal of Creation 6(2):144, 1992. Return to text.
  99. Beasley, ref. 98, p. 147. Return to text.
  100. Holloway, R.L., The poor brain of Homo sapiens neanderthalensis: see what you please … in: Delson, E. (Ed.), Ancestors: The Hard Evidence, Alan R. Liss, New York, pp. 320–321, 1985. Return to text.
  101. Lubenow, ref. 17, p. 77. Return to text.
  102. Lewin, ref. 36, p. 179. Return to text.
  103. Lubenow, ref. 17, p. 258. Return to text.
  104. Lubenow, ref. 17, pp. 82–85. Return to text.
  105. Cuozzo, J., Buried Alive: The Startling Truth about Neanderthal Man, Master Books, Green Forest , AR , pp. 166–167, 1998. Return to text.
  106. Cuozzo, ref. 105, pp. 41–42. Return to text.
  107. Shipman, P., On the origin of races, New Scientist 137:34, 1993. Return to text.
  108. Wolpoff, M. and Caspari, R., Race and Human Evolution, Simon & Schuster, New York, pp. 331–332, 1997. Return to text.
  109. Stringer, C. and Gamble, C., In Search of the Neanderthals: Solving the Puzzle of Human Origins, Thames and Hudson, London, p. 219, 1993. Return to text.
  110. Lubenow, ref. 17, p. 80. Return to text.
  111. Cauchi, S., Lost race of human ‘hobbits’ unearthed on Indonesian island, The Age, p. 1, 28 October, 2004. Return to text.
  112. Wieland, C., Soggy dwarf bones, 28 October 2004. Return to text.
  113. Morwood, M.J. et al., Archaeology and age of a new hominin from Flores in eastern Indonesia, Nature 431:1091, 2004. Return to text.
  114. Brown, P., Sutikna, T., Morwood, M.J., Soejono, R.P., Jatmiko, E., Saptomo, W. and Due, R.A., A new small-bodied hominin from the late Pleistocene of Flores, Indonesia, Nature 431:1055–1061, 2004. Return to text.
  115. Leakey, L.S.B., Tobias, P.V. and Napier, J.R., A new species of the genus Homo from Olduvai Gorge , Nature 202:7, 1964. Return to text.
  116. Holloway, ref. 20, p. 107. Return to text.
  117. Passingham, R.E. and Ettlinger, G., A comparison of cortical functions in man and the other primates, International Review of Neurobiology, 16:257, 1974. Return to text.
  118. Aiello, L. and Dean, C., An Introduction to Human Evolutionary Anatomy, Academic Press, London, pp. 189–191, 1990. Return to text.
  119. Brown et al., ref. 114, p. 1060. Return to text.
  120. Knight, W. and Nowak, R., Meet our new human relatives, New Scientist 184(2471):8, 2004. Return to text.
  121. Brown et al., ref. 114, pp. 1060–1061. Return to text.
  122. Knight and Nowak, ref. 120, p. 9. Return to text.
  123. Dalton, R., Little lady of Flores forces rethink of human evolution, Nature 431:1029, 2004. Return to text.
  124. Wieland, C., Hobbling the Hobbit, 8 November 2004. Return to text.
  125. Balter, M., Skeptics question whether Flores hominid is a new species, Science 306:1116, 2004. Return to text.
  126. Aglionby, J. and McKie, R., Hobbit folk ‘were just sick humans’, https://www.theguardian.com/world/2004/nov/07/science.indonesia, 9 November 2004. Return to text.
  127. Beasley, ref. 98, pp. 142–143. Return to text.