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    15 December 1995, Volume 14 Issue 04
    Thoughts on the whole course of human evolution
    Wu Rukang
    1995, 14(04):  285-296. 
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    Most papers on paleoanthropology are devoted to the descriptions of certain human fossil finds or to a certain stage of human evolution, but very few concerns the whole course of human evolution. Here I try to present my thoughts on it with the following sections:
    1 The transition from ape to human
    I proposed in 1970's that there exists a transitional period from ape to human. The distinctive human traits arise successively in this period and no one single trait can be considered as the marker between ape and human. Here I will further elaborate this idea.
    This period begins with upright posture and ends with the making of tools, the human society formed alongside. Self-consciousness and speech conceived before the tool-making. The creature of this period or "pre-human" can walk upright, constantly use natural wood sticks or stones to get foods and defend itself, leads a life of primitive social group with promiscuous sexual relations. In classification, they belong to the family Hominidae.
    2 Punctuated equilibria or gradual evolution
    Whether human evolution follows the models of punctuated equilibria or phyletic gradualism? It is an interesting question.
    It is generally recognized that the course of human evolution starts from the pre-human (represented by the Australopithecine fossils) to Homo habilis, then to Homo erectus and finally to Homo Sapiens. The transition from A. afarensis to H. habilis is marked by considerable morphological continuity. The latest A. afarensis is 3 million years and the earliest Homo habilis is 2.4 million years old. No fossils had been found in the interval of 0.6 million years, but it can be inferred that this is the period for the changes of A. afarensis into Homo habilis. It seems to be an example of stasis and punctuation.
    The earliest Homo erectus so far found in the Old World is a little less than 2 million years old. Their interrelations are not clear yet. They seem to have appeared almost abruptly and lasted very long time until 200,000 years ago. During this long period, they changed very little in morphology. Their implements also improved little. No significant trends can be observed and that stasis had occurred for over a million years before rapid evolutionary change began toward the end of the Middle Pleistocene.
    3 Unbalanced development of physical features in human evolution
    When I reviewed the physical features of Peking Man or Peking Homo erectus in 1960, I pointed out the unbalanced development of physical features in the course of human evolution and put forward an explanation (Woo Ju-Kang, 1960).Peking Homo erectus can already adopt an erect posture, has limbs and trunk fundamentally similar to those of modern humans, but with a somewhat ape-like head. As to the limb bones, the upper extremity is almost identical with that of modern humans, while the lower extremity, though similar to that of modern humans, still possesses some primitive characters.
    The physical features of Peking Homo erectus may be simply and figuratively said to have a body like that of modern human combined with a primitive and somewhat ape-like head.
    Not only the Peking Homo erectus is such a queer character, but the other early hominids also have similar forms.
    How to explain these phenomena?
    It is interesting to note that the principle of the mosaic mode of evolution is also applicable to the transition from the ape to human. Australopithecus, Homo habilis and Homo erectus all show mosaic features of modern humans and modern apes.
    The upper extremity differentiates first and foremost toward the direction of modern human. Owing to the manipulation of the hands, the upper extremity differentiates faster than the lower one and hence the latter lags behind the former in the development toward the direction of modern human. The differentiation of extremities is followed by the development of the brain and the brain case, so the skulls and jaws still retain many primitive characters. The big brain of modern human is achieved in the long process of using and making of tools.
    The process of human evolution demonstrates that, due to the constant use of hands for production, the extremities differentiate earlier than the development of brain. In western countries many people still believe that the swift advance of civilization was ascribed to the mind, to the development and activity of the brain, and mind is the motive force in human evolution. This idealistic outlook is refuted by the foregoing facts.
    4 Evolution of modern humans
    In human evolution, it generally deals with how early humans were evolved to modern humans, and did not touch the problem of the evolution of modern humans. Is modern humankind still evolving? If so, how is it evolved?
    In 1990, I sugested that the evolution of modern humankind was expressed in two aspects: the extra-body evolution and the spiritual evolution. I elaborated it further in this paper.
    Thoughts on Homo erectus and its place in human evolution
    Phillip V.Tobias
    1995, 14(04):  297-312. 
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    The current picture of hominid evolution in Java
    D.E.Tyler
    1995, 14(04):  313-323. 
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    Of the four major geographical areas where fossil hominids are found, Southeast Asia is the least understood. Except for some isolated teeth the only fossil hominid remains are from sites near the Ngandong (Solo) River of Java. All of the major discoveries of Homo erectus have been made by local farmers except for the original "Pithecanthropus" find of 1891.In 1949, based on the large size of a single mandible, G.H.R. von Koenigswald named a new hominid genus 'Meganthropus.' Today there is no agreement among the authorities concerning the taxonomic status of the mandibular specimens that have been assigned to the genus, "Meganthropus.' Despite morphological differences mostly related to extreme size, these mandibles have been assigned by most authorities to a proposed highly sexually dimorphic population of early H. erectus in Java. New evidence of cranial material has made this proposal even more problematic. Sangiran 31 consists of nearly complete left and right parietals, part of the left temporal, and an occipital. The overall morphology is different from any known specimen of H. erecrus. An undescribed specimen, Sangiran 27, consists of a nearly complete but crushed cranium. The palate and dentition are intact and are within the size range found for the "Meganthropus" type specimen and outside the range of known H. erectus specimens. It also possesses a double sagittal ridge. “Meganthropus" may be valid and represent an additional hominid genus in Southeast Asia.
    Environmental variability and its effect on hominid evolution
    Richard Potts
    1995, 14(04):  324-339. 
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    Early hominids have long been considered to have evolved in response to a directional shift from forested to open habitats (e.g., woodland, savanna grassland, glaciated terrain). Long-term paleoenvironmental records during the span of hominid evolution, however, contradict the idea of a simple directional trend followed by open-habitat stability. Rather, evidence from deep ocean cores, paleovegetation, and paleolakes all suggest a high degree and erratic pace of environmental fluctuation. The degree of fluctuation was higher during the period of hominid evolution than any earlier time during the Cenozoic. Thus adaptation to disparity, or to the conflicting demands posed by natural selection, may provide a better explanation of hominid evolution than adaptation to a single directional trend or stable environment. An example from the Pleistocene of southern Kenya illustrates how species survival and change may have been affected by environmental variability.
    Recognizing ash deposits in the archaeological record: A mineralogical study at Kebara and Hayonim Caves, Israel
    S.Weiner, S.Schiegl, O. Bar-Yosef
    1995, 14(04):  340-351. 
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    Preserved ash in the archaeological record constitutes an important source of information on the manner in which fire was used by hominids. Recognizing fossil ash deposits is difficult, because ash is not stable in most environments, but undergoes a series of diagenetic alterations. Here we review the mineralogical transformations that ash deposits underwent in two caves in Israel. We note that a relatively stable component of ash, at least in these environments, is the siliceous aggregate fraction. Its presence in bedded layers within the stratigraphic sequence at other sites may constitute good evidence for the presence of fossil ash deposits.
    Paleoanthropological evidence of language from East Asia, Africa and the Pacific
    Lynne A.Schepartzl
    1995, 14(04):  352-359. 
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    The study of complex language evolution is primarily based upon the European paleoanthropological record. Data from other world regions are often ignored or dismissed as European-derived. While the East Asian, sub-Saharan African and Australian evidence shows some marked similarities with the more extensive record from Europe, there are also striking contrasts. Most notably, burial appears to be a much later phenomenon outside Europe and the Levant, but rock art from sub-Saharan Africa and Australia predates European examples. These differences are most likely due to environmental and recovery factors, and do not provide evidence for any fundamental disparities in complex language capacities among world populations during the Palaeolithic.
    The dental morphology of the Neolithic humans in North China and its relationship with modern Chinese origin
    Liu Wu
    1995, 14(04):  360-380. 
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    The purpose of this research is to study the dental morphology of the neolithic humans in north China and its relationship with modern Chinese origin. The dental specimens used in this research include the neolithic human teeth from Xiawanggang in Henan province and Miaozigou in Inner Mongolia, which were observed by present author. The dental morphological data of some other Asian populations cited from references were also used including the people of Shang dynasty from Anyang and people of south China. In order to study the temporal changes of certain dental traits, some fossil teeth found in China were also used. The results are as follows:
    1. The frequencies of most dental morphological traits of the neolithic humans in north China are quite similar to those of other NE Asians and are different from SE Asians. This is especially true in traits of shovel incisor, double-shovel incisor, enamel extension of upper molars, deflecting wrinkle of lower molars and three roots of lower first molar.
    2. The temporal changes of certain traits were studied by observing some fossil teeth found in China. Some traits were found to have existed as early as Homo erectus and evolved till modern humans, for example shovel incisor, double-shovel incisor, interruption groove, peg/ reduced/ congenital absence of M3, and deflecting wrinkle. No fossil teeth have enamel extension suggesting this trait occurred only on the teeth of anatomically modern humans. The trait of three roots of lower first molar was found on the mandible of Homo erectus excavated at Zhoukoudian in 1959.
    3. Statistical analyses show that the inhabitants of the two sites have closer biological distance with Anyang and other NE Asians than with SE Asians. Cluster analysis indicates there are two population systems in E Asia corresponding to the distribution of Sundadonty and Sinodonty.
    4. According to the morphological observation and statistical analyses mentioned above, it seems that Turner's theory of existence of two types of dental morphological traits in east Asians cannot be denied. However, some phenomenons revealed in this research cannot be explained with his idea. So further research is necessary to demonstrate the formation, relationship of the two types of teeth and their roles on modern human origin in this area. The analyses of the distribution and evolution trend for some dental morphological traits indicate: the research of dental morphology will help us clarify the course of the origin and evolution of modern humans in China.
    Hominid studies in South Africa
    Wu Rukang
    1995, 14(04):  382-386. 
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