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    15 June 2006, Volume 44 Issue 02
    Quaternary environmental changes and evolution of large mammals in North China
    Qiu Zhanxiang
    2006, 44(02):  109-132. 
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    Preparation and publication of GTS 2004 led the discussion on the concept, time duration and rank of the " Quaternary" to a new height. Pending the final ratification, it seems almost certain that its lower boundary is to be lowered to —2. 6 Ma, but its rank as Period or Sub-Era remains to be decided. At any rate, the " Quaternary" will encompass 3 major units: the late Pliocene, Pleistocene and Holocene, which are chiefly based on marine deposits. The " Quaternary" large mammals of North China has been extensively studied for a long time. Now it is advisable to review their evolution in light of the new perspective. Tentative analysis of the available paleoenvironmental data in conjunction with the evolutionary phases of the mammalian faunas shows the following: 1) —2. 6 Ma is certainly a critical period, at least in North Asia, when a number of events concurred. These include the great expansion of the Arctic ice sheet, the beginning of large-scaled loess deposition induced by intensification of monsoon system, and the extinction of large numbers of typical Hipparion fauna by —2. 6 Ma. 2) 2. 6 l. 3 Ma is a period flourished with archaic types of " Quintenary" large mammals. As immigrants from North America, Equus and Megantereon entered Eurasia at the beginning of the period. Large numbers of typical “Quaternary” genera appeared, like Eirictis, Metes, Crocuta, Coelodonta, Eucladoceros, Elaphurus, Leptobos, etc. Climate of this period, especially its later half, was comparatively stable, rather mild in general, as shown in Ding et al. 's Chiloparts. 3) l. 3 —0. 13 Ma is characterized by particular development of Sinomegaceros. Typical Middle Pleistocene species as typified by ZKD fauna appeared, like Canis variabilis, Pachycrocuta sinensis, Megantereon inexpectatus, Dicerorhinus kirchbergensis, etc. A peculiar aspect is the invasion of Oriental elements into the south part of the North China, like Ailuropoda, Stegodon orientalis, Megatapirus, Elaphodus, Capricornis, etc., at the very beginning of this period. Climate of this period was highly variable, with at least 3 cold and one prolonged warm episodes (LIS, L9, L2 and S5 in Chiloparts). Therefore, this period might be further subdivided when in-depth study is carried out in the future. 4) 0. 13 — 0. 011 Ma is characterized by a mixture of survived coldadapted forms with living species. Climate of this period was probably mild. Such a climatic condition might have caused the adaptive radiation of the survived cold-adapted forms, as exemplified by the bizarre-antlered giant deer. 5) 0. 011 Ma Recent is equivalent to Holocene. Its mammalian fauna became modernized, with the final extinction of holdovers of the glacial period exemplified by mammoth and woolly rhinoceros. We suggest that the above 4 phases be designated from earliest to latest as NCMQ1~ 4. The NCMQ1 —2 boundary does not coincide with that of Plio-Pleistocene (1. 8 Ma), neither with that of Early-Middle Pleistocene (0. 78 Ma). However, such a subdivision is rather close to the subdividions based on mammals currently adopted in North America and Europe. The Blancan-lrvingtonian boundary (in N ALMA) lies at — 1. 35 Ma. The upper boundary of the European Villafranchian lies also between l. 4~ 1. 1 Ma.
    Chinese Late Neogene land mammal community and the environmental changes of East Asia
    Zhang Zhaoqun
    2006, 44(02):  133-142. 
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    Based on the present available fossil mammal data, this paper tries to synthesize the most updated publications on the Chinese late Neogene, and analyze the evolutionary process of fossil mammal communities and their response to climatic and environmental changes. Preliminary results show that fossil mammal communities in North China are rather stable and uniforrn from the end of Middle Miocene till the latest Miocene (ca. 13 Ma to 7 —8 Ma). The differentiation of a humid and closed fauna in the east, a dry and open fauna in the west during the latest Miocene might be closely related with intensification of the East Asian summer monsoon. Fossil mammal dispersal evidences from Tibet and adjacent areas suggest the forrnation of a geologic ban-ier due to uplift of the Tibet Plateau that might also be the cause of intensification of the East Asian summer monsoon. The Pliocene faunas from North China show strong adaptation to open and dry environments. The diversification and dominance of some lineages, such as siphneids and ochotonids, may well be explained by the climatic vibration during the late Pliocene. Due to the incompleteness, unevenness, and poor geographic coverage of mammal fossils, more work is wanting for achievement of this important and interesting issue discussed herein.
    Chinese Neogene mammal biochronology
    Deng Tao
    2006, 44(02):  143-163. 
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    Seven land mammal ages and thirteen mammal faunal units ( NMU) are recognized for the Chinese Neogene based on updated large and small mammal faunas. Nowadays, NMU has been strongly broadened by data from new localities and new taxa in China. The significance of these new data is that they are beneficial toward our understanding of mammal turnovers and boundary calibrations. In recent years, the Chinese Neogene mammal ages have become more accurate with the introduction of magnetostratigraphy, which has enabled ages to be calibrated and well-dated at their boundaries. Increasingly abundant paleomagnetic measurements make a good calibration for the correlation of the Chinese Neogene mammalian faunas with their European countelparts. As a result, this paper compares and corelates NMU to the European Neogene mammal zones ( MIN) , based primarily on mammalian fossils and paleomagnetic datings.
    Faunal succession and biochronology of the Miocene through Pliocene Nei Mongol (Inner Mongolia)
    Qiu Zhuding, Wang Xiaoming, Li Qiang
    2006, 44(02):  164-181. 
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    Neogene terrestrial deposits with rich fossil record are widespread in central Nei Mongol. The paucity of demonstrable superpositional sequence of assemblages and the lack of absolute dates , however, make recognition of the faunal succession and dating of the biochronology rely mainly on studies of faunal composition and evolution. The diversified faunas and new discoveries made in the last more than 20 years in this area afford an opportunity to further understand the phylogeny of mammals. The present work reviews the faunas, presents the updated faunal lists, and defines the biochronology through the analysis of the assemblages, although magnetostratigraphy is also considered when available. The faunal succession in the central Nei Mongol has assumed a prominent place in the development of a biochronology for the Neogene, covering parts of the Miocene Shanwangian , Tunggurian and Baodean, and the Pliocene Yushean of the Chinese Land Mammal Age. Informal subdivisions are suggested for Tunggurian and Baodean where it seems clearly indicated by the faunal succession. Although we are not able to propose boundary definitions for these ages, we utilize the first appearance and last occurrence of certain taxa in this region to characterize each age. Continued study of the succession , including discovery of new assemblages, will provide more data for the refinement of the biochronologic scale in this area, and for the establishment of more precise Neogene geochronologic subdivision in China.
    Evolution of the Diatomyidae, an endemic family of Asian rodents
    Lawrence J. FLYNN
    2006, 44(02):  182-192. 
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    The Diatomyidae are a distinctive rodent family of Asian distribution. The skull is characterized by hystricomorphous musculature, and the jaw is sciurognathous in momphology. The group represents a local radiation of ctenodactyloid rodents closely related to, but not a member of Hystricognathi. The fossil record first yields Diatomyidae in the Oligocene terrestrial sediments of Baluchistan, followed by younger occurrences elsewhere in the late Oligocene of southern Asia. Successive deposits of the Indian subcontinent illustrate much of what is known of the history of the family. By the late Early Miocene and Middle Miocene, Diatomyidae are also known from Thailand, China, and Japan. Thereafter, diatomyids are rare and infrequently recorded as fossils. One taxon is known from the early Late Miocene of Pakistan, and there is a possible record in the late Miocene of southern China. Although abundant where found in the oldest fossil sites, diatomyids are not numerous as fossils in later localities, except Li, Thailand. This suggests special habitat preference or bias against preservation at sites where they do occur. The known fossil record does not indicate taxonomic diversity of the group, but this may be an artifact of lack of fossilization. Survival of Diatomyidae as specialized rodents of habitat peripheral to fluvial systems is consistent with the hypothesis that the recently recognized extant Laonastes of rocky terrain in central Laos is a diatomyid.
    Review of recent advances on study of Mesozoic mammals in China
    Wang Yuanqing, Hu Yaoming, Li Chuankui
    2006, 44(02):  193-204. 
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    Twenty-six named species of 23 genera have been known in China from the deposits ranging from the Early Jurassic to Late Cretaceous. Except a few taxa, most of recently discovered Mesozoic mammals in China are represented by well-preserved skulls and skeletons. They have greatly improved our knowledge of the relationships of the major mammalian lineages and the character transition during the evolution of early mammals. Some localities of the Jehol Biota produced most Mesozoic mammal fossils in the past several years. These fossils represent different major groups and show high diversity in body size, locomotory adaptation, and dietary. Such diversification ensures them to occupy different niches in the common ecosystem. Frequent volcanic eruptions in western Liaoning were primarily responsible for the massive death of animals. Specimens preserved in sleeping posture, like the type specimen of Repenomamus gz.ganticus, may indicate that the emission of poisonous gas with the volcanic eruption was probably involved in causing the disaster.