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    15 March 1984, Volume 3 Issue 01
    Morphological features of ramapithecus and sivapithecus and their phylogenetic relationships ——morphology and comparison of the mandibles
    Wu Rukang (Woo Ju-Kang), Lu Qingwu, Xu Qinghua
    1984, 3(01):  1-87. 
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    The fossils of hominoids bearing locality at Shihuiba, Lufeng County, Yunnan province had been digged for eight seasons during 1975—1981. Mandibles of Ramapithecus and Sivapithecus of the following were unearthed. The three comparatively complete specimens of mandibles of Ramapithecus and four of Sivapithecus and more than 20 pieces of their fragments were studied and compared with those of extant large apes and those of related fossil specimens.
    The main characters of mandibles of Ramapithecus and Sivapithecus from Lufeng are as follows:
    1. The frontal part of the symphyseal region and the frontal teeth are almost vertically oriented.
    2. The depths of the symphyseal region are large compared with those of the posterior of corpora.
    3. The alveolar planes are moderately oblique.
    4. The superior transverse tori are not pronounced.
    5. The genioglossal fossae are of medium breadth.
    6. The inferior transverse tori are strongly developed and the bottom of them slants postero-superiorly.
    7. The depths of corpora at P4 and M3 are comparatively great.
    8. The ascending rami are deep and broad and perpendicular to the corpora with their frontal margin relatively more in front.
    Comparison of mandibles from Lufeng with those of the extant great apes suggests that they differ greatly from those of gorilla and chimpanzee, but close to that of orang-utan in five points as follows:
    1. The frontal part of the symphyseal region and the frontal teeth are almost vertically oriented.
    2. The alveolar planes are moderately oblique.
    3. The superior transverse tori are not pronounced and the breadths of genioglossal fossae are medium.
    4. They are well-matched in the depth and broadness of posterior parts of corpora and the relation of proportion in depth at the symphyseal region and the lateral part of corpora are comparatively similar between the Sivapithecus from Lufeng (PA 820) and the male orang-utan (No. 925).
    5. The depth of ascending ramus of Sivapithecus from Lufeng corresponds to that of male orang-utan and the relation of proportion is comparatively similar between the depth of ascending ramus and that of corpora.
    These resemblance between both further indicates that the two types of hominoids from Lufeng are most similar to orang-utan among the living great apes.
    The mandibles of hominoids from Lufeng especially Ramapithecus when compared with those of Australo pith ecus present the following main similar characterisitics.
    1. The frontal part of corpora and the frontal teeth are almost vertically oriented.
    2. The sizes of frontal teeth particularly canines, are small and vertically oriented.
    3. The cheek teeth are megadontic (relative to body size) with very thick enamel.
    4. The bottoms of inferior transverse tori are oblique postero-superiorly and strongly projected backward.
    5. The ascending rami are deep and broad.
    In short, their common features are: their dentition possesses strong function of cutting and grinding; there are massive mandibular buttresses—the inferior transverse tori in inner side of the symphysis, and the ascending rami are deep and broad. These features may be the result of eating rough diet.
    As many characteristics of two kinds of hominoids from Lufeng are similar to those of orang-utan, it seems to indicate that they have close relationships. These two kinds probably belong the same species with great sexual dimorphism. On the other hand, Ramapi- thecus from Lufeng also shows some features similar to Australopithecus. Thus, there is also possibility that Ramapithecus is a different taxon from Sivapithecus, and it is nearer to the common stock of man and African large apes.
    Human fossil and paleolithic remains from Jinchuan, Gansu
    Liu Yulin, Huang Weiwen, Lin Yipu
    1984, 3(01):  11-90. 
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    This paper deals with the materials including a less complete skull cap of Homo sapiens associated with the remains of fossil mammals and stone artifacts from two localities in Jinchuan, Gansu.
    Their geological age determined by the remains of fossil mammals especially the Myo- s pal ax fontanieri, may be Upper Pleistocene.
    The skull cap characterized by its thinness and by the development of a protuberance on the occipital bone etc., is indistinguishable from that of Homo sapiens. The owner of this skuil cap might die in her twenties, as the sagittal suture between the foraminas was closed.
    The paleolithic assemblage includes choppers, scrapers, points, bolas, cores and flakes. The direct percussion by a striking hammer and bipolar methods were applied in the flake detachment process. AH of the stone tools were made by the way of direct percussion.
    The characters of this paleolithic assemblage are similar essentially to that of the paleolithic assemblage from the sites of Nanyugou, of Taoshanzui, of Zhangwu and of Liujia- cha which are also located in the Jing valley as this paper dealt with. We think they belong to the same culture tradition.
    Judging on the study of fossil mammalian fauna, the geological age of these sites is comparable either with that of Sala-wushu (foremerly Sjara-osso-gol), ca. 50,000—37,000 y. BP, or that of Shiyu, ca. 28,945 ± 1,370 y. BP, and younger than the age of Dingchuan which represents tke early stage of Upper Pleistocene in North China.
    A preliminary study of the second excavation of Dali man locality
    Zhang Senshui
    1984, 3(01):  19-92. 
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    In autumn 1980, we organized the second systematic excavation of the Dali Man locality, It was in September and October that the excavation was undertaken, as a result of which 384 artifacts and some mammalian fossils were found from layer 3 of the Dali man locality. Besides, we have newly found two layers bearing some artifacts and a few mammalian fossils (i.e. layers 4 and 5 of the same locality). A preliminary study of the new materials is made in this note.
    13 artifacts and some mammalian fossils such as Sinomegaceros cf. pachyosteus and Equus hemionus etc. were uncountered from layer. 5. 2 cores, 2 flakes and some fossils such as Lamprotula sp. and Cervus canadensis (left antler) were discovered from layer 4.
    In view of mammalian fossils associated with the artifacts from layer 3 of the Dali Man locality, there are both Sinomegaceros cf. pachyosteus, Equus cf. sanmeniensis of the zhoukoudian period and Gazella przewalskyi and Equus sp. similar to E. hemionus and E. caballus, reported from younger deposits (Loess). Therefore, we suggest that the layer 3 of the Dali Man locality is distinctly younger than Sinanthropus site in age, and approximately contemporary to Loc. 15 in Zhoukoudian (Choukoutien) region or slightly later.
    All artifacts found from layer 3 are very small, most of them are less than 40 mm. in length. They are divided into cores, flakes, scrapers, points, gravers and awls, but no choppers have been gathered in our collection. The cores and the flakes were mostly made by hammer direct method, but a few pieces of them were produced by bipolar way in this assemblage. Most of the tools were retouched on one surface, some of them were chipped on two surfaces. Generally speaking, the artifacts show more rudely.
    In broad outline, this industry is more close to the Sinanthropus industry. A detailed study of the artifacts found from this locality is now under way.
    The measurements of some Chinese (Qingdao district) cranial angles
    Wang Ruxin, Bao Mingxin
    1984, 3(01):  32-36. 
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    1.Sixteen angles of 304 adult skulls of known sex (male 153, female 151) collected in Qingdao district of shangdong province were measured.
    2. The sex differences of some cranial angles were discussed.
    3. The measurements of present sample were compared with Han nationality of Hunan Province and there is no significant difference bo tween them.
    Dermatoglyphic studies on eleven national minorities in china I. Hnger print
    Li Shizhe, Mao Zhongrong, Xu Jiujin, Yuan Yida, Li Shaowu, Du Ruofu
    1984, 3(01):  37-43. 
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    Finger patterns and finger ridge count were studied on 5,013 samples from 11 national minorities (12 populations) in China. Several basic parameters were calculated, and the difference between sexes, left and right sides, nationalities and races, as well as the characteristics in distribution of finger patterns and finger ridge count were compared and analysed. The study shows that the finger patterns of these nationalities have both their own feature and the general character of the Mongoloid.
    Dermatoglyphic studies on eleven national minorities in china Ⅱ. Palmar print
    Li Shizhe, Mao Zhongrong, Xu Jiujin, Yuan Yida, Li Shaowu, Du Ruofu
    1984, 3(01):  44-52. 
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    Palmar print samples of 5,013 people from 11 Chinese national minorities were studied. The a-b ridge count, atd angle count, palmar flexion crease patterns, palmar true patterns and palmar main line were studied and calculatel, and the difference between sexes, left and right sides, nationalities and races were analysed. The palmar print of each nationality shows both its own feature and the general character of the Mongoloid.
    First discovery of ursavus in China and note on other ursidae specimens from the ramapithecus fossil site of Lufeng
    Qi Guoqin
    1984, 3(01):  53-94. 
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    The paper deals with the description of the Ursidae specimens from the Ramapithecus fossil site of Lufeng. Three kinds of the Ursidae fossils were collected by the Lufeng Team in 1981: Ursavus depereti, Indarctos sinensis and Ursinae.
    The fossil materials of Ursavus depereti include a broken right DP4, a broken left M1 and right M1, a broken left M2 and right M2, a complete right M2; a piece of left tooth row with P3—P4, a broken right P4, a broken right Mi, a piece o£ right tooth row with M2—M, a complete left M3.
    DP4 The paracone relatively bigger than the metacone. The deutercone ridge-like. There is a small basin between the posterior part of the paracone and deutercone. Many wrinkles on both internal and external sides of the cusps.
    Upper molars moderately elongate, low-crowned, with reduced main cusps and prominent internal cingulum, the occlusal surface much wrinkled.
    M1 The External cusps higher than that of the internal side. The paracone higher than the metacone. The paracone protrudes antero-externally. The metacone relatively small and connecetd to the hypocone by a cross-crest. The internal cusps fused into a wedge-like ridge.
    M2 The external border of the metacone considerably reduced relative to paracone border. The talon somewhat developed.
    P3 and P4 with double roots. The main cusp developed, with a distinct anterior accessory cusp and a faint posterior accessory cusp. The internal cingulum developed.
    Mi The paraconid relatively large. The paraconid-protoconid forming shear. The metaconid relatively small. The talonid broken.
    M2 Short antero-posteriorly relative to Mi. The trigonid broad relative to the talonid. The metaconid is more prominent than the protoconid. The external and internal borders slightly constricted postero-medially.
    M3 Small, nearly circular. Three cross-ridges run from the protoconid to the centre ot the tooth.
    Only a dight M3 of Indarctos sinensis was found from Lufeng. It is nearly circular. There is a system of enamel wrinkles on the occlusal surface. The middle field is surrounded by a slightly raised wall without any distinct cusps. Only the protoconid forms a ridge swelling bounded posteriorly by a notch. Two short ridges run from the protoconid to the centre of the field. There are six small shallow vertical grooves which are equal distance each other on the internal wall of the tooth. The length and breadth of the tooth crown are 18.5 mm and 17.0 mm respectively.
    The specimens of the Ursinae include a piece of fragment of upper jaw with a deciduous premolar, two left M1 and a right M1. Three broken lower canines, a left Pi and P2, a piece of left tooth row with P3-M1, a right P4, a broken right Mi and a right M2. The chada~ cters of Mi and M2 were discussed in the paper.
    Mi The trigonid longer than the talonid (ratio of the length of trigonid/the length of the talonid 1.7/1). The latter is broader than the former. Without cingulum and any accessory cusplets.
    M2 The length smaller than that of Mi. Its maximum width is at the middle of the trigonid and it tapes slightly posteriorly. The long axis of the tooth is somewhat curved. The external wall is concave and the internal, convex. The protoconid and metaconid are the largest cusps. A transverse ridge from the protoconid to the metaconid is interrupted by the deep valley between the cusps. The trigonid consists of four cusps: the protoconid, the metaconid, the small paraconid and another small cusp at the antero-extemal comer of the tooth. The talonid with five cusps: two lie on the external border, two on the internal border, the fifth on hind border. In comparison with M2 of Protursus, they seem to have some resemblances, but the size of the former much bigger than that of the latter. In comparison with U. boeckhi and U. edensis, their size of Mi and M2 is about same and Mi longer than M2, but the trigonid broaded than the talonid in the specimen of Lufeng, the trigonid narrower than the talonid (in U. boeckhi )or both subequal (in U. edensis).
    The specimens of Lufeng were not referred to any genus and species in this paper. If they are referred to Ursus, it is difficult to explain in age and horizon because they were excavated from the same layer with Ursavus and Indarctos mentioned above. If they are referred to Protursus, its size is too big on the one hand, and the establishment of Protur- sus itself is still a problem on the other hand. Thenius (1977) suggested that it was neither the earlist and most primitive representative of the Ursinae nor a member of the Ursidae. Protursus is a junior synonym of the genus Simocyon. In my opinion, it is undoubted that the specimens of Lufeng is a member of Ursidae even if Protursus is Simocyon. There is a clear pressing trace on the hind wall of its M2. This is a mark of connection to M3. Its phy- letic position may correspond to Protursus.
    Hexian fauna: correlation with deep-sea sediments
    Xu Qinqi, You Yuzhu
    1984, 3(01):  62-67. 
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    Hexian fauna contains some typical members of the Ailuropoda-Stegodon fauna in South China. However, there are a lot of northern members of Zhoukoudian fauna, for example, Scaptochirus, Trogontherium cuvieri, Cricetulus variant, Microtus branstioides, Tamias wimani, Ursus acctos, Megaloceros pachyosteus, Pseudaxis grayi; and some western mountainous animals, such as Anourosorex squamipes, Blarinella quadraticauda, Eothenomys eva and E. proditor. It seems to us that Hexian fauna represents a cold climate that may have caused many northern and western elements to migrate to southern China.
    However, the existence of many typical southern elements, such as Alligator cf. sinensis, Stegodon orientalis, Tapirus sinensis, Megatapirus, Macaca, Miniopterus schrebersii, Rat- tus rattus, R. ed ward si, and Eothenom.s melanogaster indicates that the climate would not be very cold, because it is unlikely that these animals could have endured very low temperature in Hexian County during Hexian Man's time. In respect to the mean annual temperature it can be assumed that it was about 12° C corresponding to that of the present day in the southern parts of North China, where most of the Hexian fauna have their living representatives. Besides, the climate would be more humid than that of North China today, for the mammalian assemblage of Hexian fauna shows, as a whole, a dominance of animals of moist- and water-loving.
    As to the fauna, the presence of some oldtimers, such as Trogontherium cuvieri, Megaloceros pachyosteus, and Homotherium, shows that it may correspond to Zhoukoudian fauna. However, the percentage of the recent species is 66% in Hexian fauna. It is interesting that the percentage of the recent species in some famous Late Pleistocene mammalian faunas is smaller than 66% or approximates to it. For example, the percentage of the recent species in Dingcun fauna is 59%, that o Xujiayao fauna is 58%, that of Salawusu fauna is 67%, and that of Shiyu fauna is 60%. If we calculate the percentage of the recent species for both micromammalian and megamammalian respectively, that is 52.2% in Hexian megamammalian fauna. It is only a little smaller than those of the Late Pleistocene mammalian faunas. Therefore Hexian fauna may correspond to the later Zhoukoudian fauna. It supports the view of Wu Rukang and Dong Xingren (1982).
    The later Zhoukoudian fauna includes those in Layers 3—5 at Zhoukoudian, Loc. 1. Fig. 1 indicates the specific diversity in Layers 3——11 of Zhoukoudian fauna. It is clear that Layer 5 would represent a warm stage, While Layers 3—4 correspond to a cold stage. Li Yanxian and Ji Hongxiang (1980) held that Layer 5 contained 29 forms, but still with more forest animals than grassland ones. Carnivora are abundant. In addition, there is an aquatic species in the fossil list (i.e, Trogontherium cuvieri). The rich finds have been obtained in calcareous tufas or travertines. Lithological and paleontological evidences suggest that the climate was warm and damp at the time. Just as mentioned above, Hexian fauna represents a cold stage. So it would be correlated with Layers 3— , but not with Layer 5. Besides, Hexian fauna is correlated with Layer 5 by the 13 common species, while with Layers 3—4 by the 15 common species. Therefore, both paleoclimatologically and paleontologically, Hexian fauna would correspond to Layers 3— , but not to Layer 5 in Zho- ukoudian fauna.
    In order to correlate the Zhoukoudian sequence (i.e. Layers 3—11) with the O'* record of deep-sea sediments, Xu Qinqi and Ouyang Lian (1982) has used cluster analysis and other mathematical techniques. As a consequence, Layer 5 is correlated with O18 stage 9, while Layers 3—4 correspond to stage 8. It is probable that Hexian fauna would be correlated with O18 stage 8, i.e. at about 240,000—280,000 years B. P.
    It is evident that Trogontherium cuvieri existed in O18 stage 9 (i.e. in Layer 5 of Zhoukoudian fauna) in North China, while it did survive in O18 stage 8 (i.e. in Hexian fauna) in southern China. During Hexian Man's time, many northern and western elements, such as Scaptochirus, Blarinella quadraticauda, Anourosorex squamipes, Tamias cf. wimani, Crice- lulus variant, Microtus brandtioides, Eothenomys inex, E. proditor, Ursus arctos, Megaloce- ros pachyosteus, and Pseudaxis grayi appeared in Hexian County. It was in O18 stage 8 that Trogontherium cuvieri died out in Europe and North China, and spent its last years in Hexian County.
    The fact has proved that stage 8 had rather great effect on mammalian fauna in eastern Asia. So did it in Europe (Bonifay, 1980). As a matter of fact, during the interval between Gongwangling and Chenjiawo fauna, there existed a cold stage, called Giinz in the Alps, Me- napian in Holland, the Gokenya age in Japan, probably Cassian in central Italy, O18 stage 22 in deep-sea sediments, etc, bringing about a significant change in mammalian fauna in eastern Asia. The major decline in temperature may have caused many southern elements, such as Ailuropoda, Stegpdon, Megatapirus, Tapirus, Nestoritherium, Elaphodus, and Capricornis to disappear from the North and to become restricted to southern China. Most of them survived in southern China, and only some reappeared in the North (Xu Qinqi and You Yu- zhu, 1982). We suggest that climate variations in regard to the mammalian fauna should be taken into serious consideration.
    Distribution and burying of late paleolithic culture in north China
    You Yuzhu
    1984, 3(01):  68-75. 
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    Three main types of continental sediments of Late Pleistocene can be recognized in North China: the cave deposits, the alluvial-lacustrine deposits and loess. More than two hundred mammalian fossil localities of Late Pleistocene and Late Paleolithic Sites have been investigated and excavated in recent years. The occurrence of Late Paleolithic Sites and mammalian fossils of Late Pleistocene seem to be corresponded to the stratigraphy, lithology, geomorphology and taphonomy. Artifacts and fossils are often discovered in:
    (1) the middle or lower part of the second terrace of local river and its tributaries;
    (2) the orangish sand-gravel and blackish sandy day of alluvial-lacustrine deposits;
    (3) the bottom of gravel under the Malan loess in the loess plateau;
    (4) the piedmont of hill which stretches into the alluvial basin or plain.