首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 31 毫秒
1.
We describe a new extinct subspecies of the Javan lutung—Trachypithecus auratus sangiranensis—based on an isolated, tooth-bearing upper jaw. The specimen was in volcanic breccia situated between the Lower Pucangan and the Upper Kalibeng Formations 500 m south of the village of Sangiran, near Surakarta, central Java, Indonesia. The new fossil monkey bears morphological similarities to the two living species of leaf monkey from Java, Presbytis comata comata and Trachypithecus auratus auratus, and to the Middle Pleistocene form, Trachypithecus cristatus [=auratus] robustus, from Tegoean, central Java. It is significantly larger than any of these forms, and differs from them in details of dental anatomy. Because the greatest number of similarities are between the new fossil and Trachypithecus auratus subspecies, we designated the specimen as T. a. sangiranensis. The geochronological age of the breccia from which the fossil came, is 1.9± 0.05 Ma (million years), making T. a. sangiranensis one of the oldest fossil monkeys from eastern Asia.  相似文献   

2.
There are now eleven manidublar pieces from the Lower and Middle Pleistocene of Java, all but one being from the Sangiran site. All of these have been assigned toHomo erectus by most workers, while others have suggested as many as four different hominoid taxa. Sangiran 21 (Mandible E), Sangiran 22 (Mandible F), and Sangiran 37 (Mandible G) are described here fully for the first time. Sangiran 21, 22, and 27 all come from the Upper Pucangan Formation and date approximately 1.2 Myr. The new mandibles are morphologically compatible with theH. erectus, crania from Java.  相似文献   

3.
This article reviews palaeoanthropological research in Indonesia since 1889 in terms of fossil discoveries. Of the three periods identified, the second one (1931–1941) resulted in more finds than the other two. Most finds are skull fragments of Pithecanthropus erectus, from the Middle Pleistocene Kabuh formation, and from the site of Sangiran. New code numbers are given to the finds to facilitate discussion, especially in the cases of previous misnumbering and controversial specimens.K/Ar dating gives an antiquity of 1·9 ± 0·4 million years for the Jetis beds at Perning (site of the Mojokerto juvenile calvaria) and 830,000 years for the Trinil beds at Sangiran (sites of Sangiran 10 and 12 calottes). Work on chronometric dating is continuing.Several re-examinations of earlier finds from Java have been performed in the last two decades. Finds during this period are reviewed and described, comprising one calvaria, two skull caps, two mandibular fragments, skull vault and base fragments, and teeth. One mandibular fragment is related to Meganthropus, but no skull fragments are associated with this to make its taxonomic status clearer. For the first time portion of the cranial base anterior to the foramen magnum and the zygomatic bone of Pithecanthropus erectus are available.The fossil finds demonstrate the genetic consistency of Pithecanthropus as revealed by the morphology of the skull. Palaeoanthropological research goes on, slowly but surely, especially in the Sangiran dome area of Central Java.  相似文献   

4.
5.
This contribution reports fifteen human fossil dental remains found during the last two decades in the Sangiran Dome area, in Central Java, Indonesia. Among this sample, only one of the specimens had already been briefly described, with the other fourteen remaining unreported. Seven of the fifteen isolated teeth were found in a secured stratigraphic context in the late Lower-early Middle Pleistocene Kabuh Formation. The remaining elements were surface finds which, based on coincidental sources of information, were inferred as coming from the Kabuh Formation. Mainly constituted of permanent molars, but also including one upper incisor and one upper premolar, this dental sample brings additional evidence for a marked degree of size variation and time-related structural reduction in Javanese H. erectus. This is notably expressed by a significant decrease of the mesiodistal diameter, frequently associated to the reduction or even loss of the lower molar distal cusp (hypoconulid) and to a more square occlusal outline. In addition to the hypoconulid reduction or loss, this new sample also exhibits a low frequency of the occlusal Y-groove pattern, with a dominance of the X and, to a lesser extent, of the+patterns. This combination is rare in the Lower and early Middle Pleistocene paleoanthropological record, including in the early Javanese dental assemblage from the Sangiran Dome. On the other hand, similar dental features are found in Chinese H. erectus and in H. heidelbergensis. As a whole, this new record confirms the complex nature of the intermittent exchanges that occurred between continental and insular Southeast Asia through the Pleistocene.  相似文献   

6.
In 1994 a hominid frontal bone fragment was found in the river floor of the Brangkal River, the Sangiran area, Central Java. The original stratigraphic level is not known at present stage of the research. But it is possible that the bone was derived from the Grenzbank zone of the Bapang Formation (Lower/Middle Pleistocene). Morphological features of the bone, such as a thick and continuous supraorbital torus, a wide and flat supratoral plane, and a flat and strongly inclined frontal squame suggest that the bone is assigned to JavaneseHomo erectus, especially to the Sangiran and Trinil group of it.  相似文献   

7.
Etty Indriati 《HOMO》2010,61(4):225-243
We describe in detail Sangiran 38 (S38), an adult partial calvaria recovered in 1980 from the Bapang (Kabuh) Formation of the Sangiran Dome near the hamlet of Sendangbusik, Java. Several other hominins (Bukuran, Hanoman 1, and Bs 9706) recovered in the vicinity come from either the upper-most Sangiran (Pucangan) or lower-most Bapang formations. S38 is from the lower Bapang Formation, which 40Ar/39Ar age estimates suggest spans between 1.47 and 1.58 Ma. Anatomical and metric comparisons with a worldwide set of ‘early non-erectus’ Homo, and Homo erectus (sensu lato) fossils indicate S38 is best considered a member of H. erectus. Although smaller in size, S38 is similar in overall morphology to the Bukuran specimen of similar age and provenance. The S38 calvaria exhibits several depressed lesions of the vault consistent with a scalp or systemic infection or soft tissue cyst.  相似文献   

8.
Currently, the human deciduous dental record from the Pleistocene deposits of the Sangiran Dome, Java, consists of only eight specimens. Here we report two deciduous crowns collected near the village of Pucung. While their precise geo-chronological context remains unknown, a provenance from the Early-Middle Pleistocene Kabuh Formation, or from the Early Pleistocene "Grenzbank Zone," is very likely. These isolated specimens consist of an upper first molar (PCG.1) and a lower second molar (PCG.2). Taxonomic discrimination of the Indonesian tooth record is difficult because of the convergence in crown size and appearance between Pongo and Homo. Accordingly, as PCG.2 still bears a concretion masking most of its features, we coupled the outer analysis of the two specimens with an investigation of their inner morphology. In addition to external characteristics, virtual imaging and quantitative assessment of inner morphology and tissue proportions support an attribution to the taxon Homo, and we preliminary allocate both specimens toH. erectus.  相似文献   

9.
D. E. Tyler 《Human Evolution》2001,16(3-4):151-158
There are now eleven known mandibular pieces from the Lower and Middle Pleistocene of Java, all but one being from the Sangiran site. All of these have been assigned toHomo erectus by most authorities, while others have suggested as many as four different hominoid taxa. Two of the mandibles, Sangiran 33 (Mandible H) and“Meganthropus”D (no Sangiran number yet assigned), are described here for the first time. The two new mandibles come from the Upper Pucangan Formation and date approximately 1.2–1.4 Myr. They are morphologically compatible with other“Meganthropus” mandibles described from Java. Despite attempts by numerous authorities to place all the Sangiran hominid mandibles in the species,H. erectus, the range of variation in metric and nonmetric features of the“Meganthropus” hominids is clearly beyond the know variation found inH. erectus. “Meganthropus” could represent a speciation from the well-knownH. erectus.  相似文献   

10.
《Comptes Rendus Palevol》2007,6(3):169-179
In the Sangiran dome (Central Java), Homo erectus and mammal fossils in fluviatile context are found in several open-air localities: Tanjung, Sendang Busik, Ngrejeng Plupuh, Grogol Plupuh, and Bukuran. Thirteen taxa of Middle Pleistocene mammals were determined. Lithic tools are rare at these sites. The origin and setting up of these mainly unpublished faunal assemblages are approached by means of methods usually applied to European and African sites in order to understand better the link between humans and animals. The mechanical action of water is responsible for these accumulations and its chemical action for their evolution.  相似文献   

11.
D. E. Tyler 《Human Evolution》2003,18(3-4):229-241
There are now eleven known mandibular remains from the Lower and Middle Pleistocene of Java, all but one being from the Sangiran site. All of these have been assigned toHomo erectus by most workers, while others have suggested as many as four different hominoid taxa. The author finds that the jaws cannot be a homogeneous sample. Morphologically, they are a mixture of undoubtedH. erectus, “H. meganthropus,” and possibly a pongid. If the jaws are allH. erectus then they have a sexual dimorphism exceeding that of modern gorillas. The case of“Pithecanthropus dubius” (Sangiran 5) is even less certain; even its hominid status is disputed. If it is indeedHomo it must be placed with the other“H. meganthropus” specimens. Its size and morphology are well beyond the known range anyH. erectus.  相似文献   

12.
Our current knowledge of the evolution of Homo during the early to middle Pleistocene is far from complete. This is not only because of the small number of fossil samples available, but also due to the scarcity of standardized datasets which are reliable in terms of landmark identification, interobserver error, and other distorting factors. This study aims to accurately describe the cranial morphological changes of H. erectus in Java using a standardized set of measurements taken by the authors from 18 adult crania from Sangiran, Trinil, Sambungmacan, and Ngandong. The identification of some obscure landmarks was aided by the use of micro-CT imaging. While recent studies tend to emphasize evolutionary conservatism in Javanese H. erectus, our results reinforce the theory that chronologically later groups experienced distinct morphological changes in a number of cranial traits. Some of these changes, particularly those related to brain size expansion, are similar to those observed for the genus Homo as a whole, whereas others are apparently unique specializations restricted to Javanese H. erectus. Such morphological specializations in Java include previously undescribed anteroposterior lengthening of the midcranial base and an anterior shift of the posterior temporal muscle, which might have influenced the morphology of the angular torus and supramastoid sulcus. Analyses of morphological variation indicate that the three crania from Sambungmacan variously fill the morphological gap between the chronologically earlier (Bapang-AG, Bapang Formation above the Grenzbank zone in Sangiran) and later (Ngandong) morphotypes of Java. At least one of the Bapang-AG crania, Sangiran 17, also exhibits a few characteristics which potentially indicate evolution toward the Ngandong condition. These strongly suggest the continuous, gradual morphological evolution of Javanese H. erectus from the Bapang-AG to Ngandong periods. The development of some unique features in later Javanese H. erectus supports the hypothesis that this Javanese lineage went extinct without making significant contributions to the ancestry of modern humans.  相似文献   

13.
Since the sixties, the National Indonesian Center for Archaeological Research, in collaboration with the Gajah Mada University, organizes field excavations on open-air sites in the Sangiran dome, one of the most famous places of palaeoanthropological discoveries in Southeast Asia. That project led to the discovery of Homo erectus more or less fragmentary fossils, and to the collection of numerous mammal fossils in open-air localities such as Tanjung, Sendang Busik, Ngrejeng Plupuh, Grogol Plupuh and Bukuran. Most of the bone assemblages from these sites come from the volcanic-sedimentary Kabuh layers (Early Middle Pleistocene) deposited in a fluvial context. The herbivores dominate the assemblages. The best-represented species are large bovids like Bubalus palaeokerabau or Bibos palaesondaicus and smaller cervids like Axis lydekkeri. The carnivore are very rare, only a Pachycrocuta brevirostris in Bukuran. The taphonomical study of the collections, involving several common and also modern methods, is among the first carried out on Javanese sites. The high degree of fragmentation is attested by the dominance of splinters among the fossils. In most sites, teeth and member extremities (autopodial) prevail. Conservation and fragmentation of fossil bones is not the same at all sites. Water action, either chemical or mechanical, is predominant, regarding the origin and the modification of the assemblages. The climato-edaphic traces like oxides and concretions are well represented on the bone surface. Different methods were applied to study transportation and to document the sites contexts in the frame of the ancient riverine paleogeography. Carnivores are almost absent in the material and traces of their action are rare, only in Bukuran and Ngrejeng. The tools are rare, only a bola in Tanjung 82 and chalcedony flakes in Tanjung 63–64. Anthropic influence is only obvious at Ngebung 2, a site in the west part of the dome, supported by fossil observation and correlated to the occurrence of lithic artefacts. This site was excavated during the 1990’s by a French-Indonesian team and it is a site of comparison for our study. Several analytical methods could be applied for the first time on Pleistocene faunal assemblages from Java, for example, the study of the fragmentation, that of fissuration and the characterization of the fluviatile transport undergone by the fossils.  相似文献   

14.
现存狒狒类(Papionin)生活于非洲(如Papio和Theropithoan)、亚洲(如Macaca)和北非(M.sylvanas)。在上新世和更新世,Theropithecus经历了从非洲到亚洲的扩散过程,在印度发现了类似化石。这次在云南中甸金沙江附近发现的下更新世狒狒化石(Papio)证明,如同亚洲猕猴和现代人类祖先一样,非洲狒狒类(Papio和Theropithecus)在同一时期从非洲扩散到亚洲。所不同的是它们没有像猕猴和人类一样生存下来。这次化石的发现对于研究以下生物学问题提供了重要依据1)探讨旧大陆猴类在上新—更新世从非洲到亚洲的扩散过程;2)研究不同旧大陆猴类的进化和环境适应性;3)为现代人类祖先在非洲—亚大陆的扩散研究提供证据;4)由于化石产地包括有人类祖先和其他动物的化石,因此,狒狒在亚洲的生态适应研究将为探讨人类在同一时期的生态适应提供证据。  相似文献   

15.
16.
Sangiran (Solo Basin, Central Java, Indonesia) is the singular Homo erectus fossil locale for Early Pleistocene Southeast Asia. Sangiran is the source for more than 80 specimens in deposits with 40Ar/39Ar ages of 1.51-0.9 Ma. In April 2001, we recovered a H. erectus left maxilla fragment (preserving P3- M2) from the Sangiran site of Bapang. The find spot lies at the base of the Bapang Formation type section in cemented gravelly sands traditionally called the Grenzbank Zone. Two meters above the find spot, pumice hornblende has produced an 40Ar/39Ar age of 1.51 ± 0.08 Ma. With the addition of Bpg 2001.04, Sangiran now has five H. erectus maxillae. We compare the new maxilla with homologs representing Sangiran H. erectus, Zhoukoudian H. erectus, Western H. erectus (pooled African and Georgian specimens), and Homo habilis. Greatest contrast is with the Zhoukoudian maxillae, which appear to exhibit a derived pattern of premolar-molar relationships compared to Western and Sangiran H. erectus. The dental patterns suggest distinct demic origins for the earlier H. erectus populations represented at Sangiran and the later population represented at Zhoukoudian. These two east Asian populations, separated by 5000 km and nearly 800 k.yr., may have had separate origins from different African/west Eurasian populations.  相似文献   

17.
18.
Metric and shape features of the Lower Pleistocene mandibular specimen ATD605 from the level 6 of Gran Dolina site (Atapuerca, Spain) are compared with a large sample of fossil hominid mandibles. The analysis shows that ATD6-5 displays a generalized morphology largely shared with both African and European Lower and Middle Pleistocene samples. However, distinctive African traits, such as corpus robustness and strong alveolar prominence, are absent in the Gran Dolina specimen. At the same time, none of the apomorphic features that characterize Middle and early Upper Pleistocene European hominids can be recognized in ATD6-5. Finally, the Gran Dolina specimen displays a remarkable position of the mylohyoid groove, only comparable to that found in immature specimens of Homo ergaster, and very rarely in adult H. sapiens. The morphology of ATD6-5 supports the hypothesis of an African origin for the first Europeans with subsequent phylogenetic continuity with Middle Pleistocene populations in Europe. These findings are consistent with H. antecessor being the last common ancestor of Neandertals and H. sapiens.  相似文献   

19.
This contribution investigates the inner organizational pattern (tooth tissue proportions and enamel–dentine junction morphology) of seven Homo erectus permanent molar crowns from the late Lower‐early Middle Pleistocene Kabuh Formation of the Sangiran Dome (Central Java, Indonesia). The previous study of their external characteristics confirmed the degree of time‐related structural reduction occurred in Javanese H. erectus, and also revealed a combination of nonmetric features which are rare in the Lower and early Middle Pleistocene dental record, but more frequently found in recent humans. In accordance with their outer occlusal morphology, the specimens exhibit a set of derived internal features, such as thick to hyperthick enamel, an incomplete expression of the crest patterns at the enamel–dentine junction (EDJ) level, a sharp EDJ topography. As a whole, these features differ from those expressed in some penecontemporaneous specimens/samples representing African H. erectus/ergaster and H. heidelbergensis, as well as in Neanderthals, but occur in recent human populations. Further research in virtual dental paleoanthropology to be developed at macroregional scale would clarify the polarity and intensity of the intermittent exchanges between continental and insular Southeast Asia around the Lower to Middle Pleistocene boundary, as well as should shed light on the still poorly understood longitudinal evolutionary dynamics across continental Asia. Am J Phys Anthropol 156:148–157, 2015 © 2014 Wiley Periodicals, Inc.  相似文献   

20.
The record of an opossum is reported here coming from a Middle–Late Pleistocene fluvial sedimentary sequence outcropping in the austral Chaco geomorphological region, Santa Fe province. Despite this family has different living forms widely distributed in South American plains, with great tolerance to diverse habitats conditions, the Pleistocene occurrence of didelphoids is very scarce and only limited to Holocene deposits sensu lato from austral pampean plains. The specimen found represents at the moment the only Pleistocene didelphoid opossum from Argentina with an accurate stratigraphical context. In a taphonomic framework, MFA-Pv 1582 shows no evidence of abrasion produced by transport, probably resulting of a very short time-transport. This intertropical form of Didelphis genus from Pleistocene sequences displays undoubtedly novel and sustancial paleoenvironmental and ecomorphological conditions to test in the austral Chaco region. Although the specimen shares a generalized didelphoid form, some morphologies in the humerus are closer with arboreal habits. In this context, added to the sedimentological and stratigraphical framework, it’s possible to suggest that subtropical conditions with some woodlands and wetlands dominate the provenance region of the fossil material, over a late Middle–Late Pleistocene interglacial period.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号