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    15 June 2011, Volume 49 Issue 2
    A NEW CYPRINID FISH FROM PALEOGENE OF NORTHERN XINJIANG, CHINA
    SU De-Zao
    2011, 49(2):  141-154. 
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    The fossil cypriniform fishes described here were collected from the Anjihaihe Formation(Paleogene) in the Manas County in northern Xinjiang, and referred to a new genus and species, Tianshanicus liui, of the family Cyprinidae. This new genus shows typical characters of the subfamily Leuciscinae, and is of great interest for studying the origin of the subfamily Leuciscinae. According to the nature of the fish-fauna and mammal fossils, the age of the fish-bearing beds is considered as late Eocene.
    A new eosauropterygian from Middle Triassic of eastern Yunnan Province, southwestern China 
    SHANG Qing-Hua, WU Xiao-Chun, LI Cun
    2011, 49(2):  155-177. 
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    A new eosauropterygian, Diandongosaurus acutidentatus gen. et sp. nov., is described based on a skeleton from the Upper Member of Guanling Formation (Middle Anisian) of Luoping County, Yunnan Province, southwestern China. This new species displays a combination of traits seen in nothosauroids (Simosaurus and nothosaurians) and pachypleurosaurs (Dactylosaurus, Anarosaurus, Serpianosaurus, and Neusticosaurus). It has an unconstricted snout, preorbital region longer than the postorbital region, and a supratemporal fenestra smaller than the orbit, as in the pachypleurosaurs. On the other hand, it bears enlarged and procumbent teeth in the premaxilla and the anterior dentary, and one or two fang-like maxillary teeth, as in the nothosaurs. In this new species, the frontals and the parietals are fused, the posterolateral process of the frontal extends posteriorly over the anterior margin of the supratemporal fenestra, the postorbital is excluded from the infratemporal fenestra by the jugal-squamosal contact, the quadratojugal is present, the clavicle has an anterolateral projection, and the three sacral and anterior caudal ribs are distally pinched off but not constricted. Unlike in most of other stem eosauropterygians, the prefrontal and the postfrontal meets each other along the dorsal margin of the orbit, the descending ramus of the squamosal reaches the articular condyle of the quadrate, caudal ribs 3 to 8 are elongate and longer than sacral ribs, and the ungual phalanxes of the pes are extremely dorsoventrally expanded. Our phylogenetic analysis suggests that Diandongosaurusis neither a pachypleurosaur nor a nothosauroid; it might be the sister group of the clade consisting of Wumengosaurus, the nothosauroids and those taxa traditionally considered as pachypleurosaurs.
    IMPORTANT FEATURES OF GEGEPTERUS CHANGAE(PTEROSAURIA: ARCHAEOPTERODACTYLOIDEA, CTENOCHASMATIDAE) FROM A NEW SPECIMEN
    JIANG Shun-Xing, WANG Xiao-Lin
    2011, 49(2):  172-184. 
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    Gegepterus changae is referred to the Ctenochasmatidae based on an incomplete specimen. The new specimen IVPP V 11972 is assigned to Gegepterus changae according to the unique features in the skull and cervical vertebrae. V 11972 is a subadult individual and further provides the morphological characteristics as the vertebrae, pectoral girdle, etc. Especially, we add to the diagnosis a unique feature, including the unique presence of two foramens on the nasal.
     NEW SPECIES OF OMEISAURUS FROM THE MIDDLE JURASSIC OF ZIGONG, SICHUAN 
    JIANG Shan ,LI Fei, PENG Guang-Zhao, YE Yong
    2011, 49(2):  185-194. 
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    Omeisaurus jiaoi, a new species of giant sauropod is described in this paper. The specimen (ZDM 5050) was discovered from the Xiashaximiao Formation of the Middle Jurassic of Zigong Dinosaur National Geopark, Sichuan. ZDM 5050 is a nearly complete skeleton. Its main features can be summarized as follows: dorsal vertebrae are tall and large. The anterior dorsal vertebrae (dorsals 1 to 6) are opisthocoelous. The pleurocoels of the dorsal vertebrate are well developed except on the 1stdorsal. The neural spines are club-like and the neural spines of the anterior dorsal vertebrae are not bifurcated. Caudal vertebrae are relatively short and thick. The anterior caudal vertebrae are slightly amphicoelous. The chevron of the 1st caudal vertebrae is connected with the 1st caudal and is shallow and small. Whereas the 1st caudal vertebrae of Omeisaurus tianfuensis have no chevron. The rib of the 1st caudal vertebrae are laterally directed, while the first caudal rib of the other species of Omeisaurusare prominently enlarged distally, being slightly fan-shaped. Humerus is long and straight, with slightly expanded proximal end and greatly expanded distal end. The deltopectoral crest is well-developed and relatively low. Femur has a slender shape, with a greatly expanded proximal and distal ends. The fourth trochanter is well-developed. The ratio of the humerus length to femur length is approximately 0.83, the ratio of the ulna length to humerus length is approximately 0.72, the ratio of the tibia length to femur length is approximately 0.63.
    A NEW ORNITHURINE BIRD (HONGSHANORNITHIDAE) FROM THE JIUFOTANG FORMATION OF CHAOYANG, LIAONING, CHINA
    LI Li, WANG Jing-Qi, HOU Shi-Lin
    2011, 49(2):  195-200. 
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    A new genus and species (Parahongshanornis chaoyangensis) of a basal ornithurine bird from the Jiufotang Formation in Yuanjiawa Town, Chaoyang, westernLiaoning Province is reported. It is morphologically most similar to the basal ornithurines Hongshanornis and Longicrusavis, two only known genera of the Hongshanornithidae by possessing a shorter wing compared to the leg and a “U”-shaped furcula that is significantly longer than wide. The new taxon can be distinguished from these two genera in having a furcula that is anteroposteriorly compressed proximally, with a deep groove along the clavicular symphysis, a sternum with two pairs of posterior excavations, and a pair of short posterior processes between the lateral trabecula and the medial ridge of the sternum, a short and robust first phalanx of the major digit, and a pubis with a distinctive pubic foot. The discovery of the new hongshanornithid from the Jiufotang Formation not only extends the temporal distribution of the Hongshanornithidae, but also provides new data for discussing the evolutionary differentiation of basal ornithurines in the Early Cretaceous.
    A NEW SPECIES OF LATE MIOCENE HAMSTER (CRICETIDAE, RODENTIA) FROM DAMIAO, NEI MONGOL
    ZHANG Zhao-Qun, WANG Li-Hua, LIU Yan, LIU Li-Ping
    2011, 49(2):  201-209. 
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    The Late Miocene witnessed the transition of cricetids from ancient to modernized taxa. Here we describe a new cricetid species, Nannocricetus wuae, from DM02, near the Damiao Village, Siziwangqi, Nei Mongol. The new species is characterized by having low crowned molars with conical shaped cusps, single anteroconid on m1 with developed labial and/or lingual flanges, very weak to absent mesolophids on m1, variable mesolophid and very reduced anterolophulid on m2, narrow and slightly bifid anterocone on M1, and relatively long M3. Differing from the pattern of Cricetodontinae,Nannocricetus wuae shows great simplification of tooth structure. There is no paracone spur, anteromesoloph, or styles on upper molars, no spur of anterolophulid or stylids on lower molars. Root numbers are conservative, three for upper molars and two for lower molars. Morphologically, the new species shows close similarity to Nannocricetus primitivus and N. mongolicus. These three species constitute an endemic group confined to North China, and show progressive evolution in the splitting of the anteroconid on m1, reduction of the mesoloph(id), and development of anterolophule(id) on m2/M2 etc. Based on the evolutionary stage of the new species and associated fossils, we tentatively suggest an earliest Late Miocene age pending further confirmation by systematic study of other taxa and the paleomagnetic data. 
    FOSSILS OF PLIOCENE HIPPARION (EQUIDAE, PERISSODACTYLA) FROM GAOTEGE LOCALITY, NEI MONGOL AND THEIR IMPLICATIONS
    Pang Li-Bo
    2011, 49(2):  210-222. 
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    The Gaotege locality is about 70 km southwest of Xilinhot and 33 km northeast of Tsagan Nor in Abag Qi(Banner) of central Nei Mongol(Inner Mongolia). The Pliocene sediments at Gaotege are about 70 m thick, and were described and divided into 8 beds by Li et al. (2003). In this paper, fossils of two species of Hipparion collected from Gaotege are described.
    A DENTAL PATHOLOGICAL DEFORMITY OF CHILOTHERIUM WIMANI FROM THE LINXIA BASIN OF GANSU, CHINA
    CHEN Shao-Kun, DENG Tao, HE Wen, CHEN Shan-Qin
    2011, 49(2):  223-228. 
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     Chilotherium wimani is the dominant species in the Late Miocene Hipparion fauna of the Linxia Basin. A sub-adult mandible belonging to C. wimani is described here. The unusual characters of this mandible are the retention of left dp4 and the morbid state of left and right p4. The left p4 exhibits anterior-posterior and labial-lingual reversion and the trigonid of this tooth is strongly tapered. The right p4 shows not only anterior-posterior reversion, but also the absence of trigonid. The retention of the left dp4 is induced likely by the abnormal growth of the left p4 germ, while the deformity of the left and right p4 may be caused by hereditary factors and/or malnutrition. The non-adaptive malocclusion would result in disadvantage in competition, and this functional disadvantage would be fatal under the likely condition of the harsh Late Miocene Linxia environment.
    LATE MIOCENE-EARLY PLIOCENE BIOSTRATIGRAPHY AND MIOCENE/PLIOCENE BOUNDARY IN DONGWAN SECTION,GANSU
    LIU Li-Ping, ZHENG Shao-Hua,  ZHANG Zhao-Qun, WANG Li-Hua
    2011, 49(2):  229-240. 
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    The Dongwan section is located near Dongwan Village, Qin' an County, Gansu Province(3458'N,10547'E). The section is a continuous eolian red clay sequence and is dated from 7.3to 3.5 Ma by paleomagnetic study. The 74.8 m long section is divided into 21 layers (0 to20) and 39 species of small mammals are found from 40 fossil levels. Based on faunal composition of small mammals, especially the myospalacines, four biozones are recognized. Biozone I covers layers 0~7, ranges magnetic polarities from upper part of C3Br.1n to thelower part of C3An.2n, and spans from 7.3 to 6.5 Ma. The mammals found in this biozone include Quyania chowi, Ochotonoma n. sp.1,O. primitia, Ochotona minor,O. lagreli, Sicista sp., Prospermophilus orientalis, Sinocricetus zdanskyi,? Kowalskia sp., Prosiphneus licenti,P.tianzuensis, Lophocricetus grabaui, Pseudomeriones abbreviatus, and Hansdebruijnia pusillus. Biozone II covers layers 8~14. It ranges from the lower part of polarity zone C3An.2n to the base of C3n.4n, and has a time span from 6.5 to 5.24 Ma. The fossils found in this biozone include Sulimskia sp., Parasoriculus sp., Paenepetenyia cf.P. zhudingi, Ochotonoma n.sp.2,O. primitiva, Ochotona minor,O. gracilis,O. plicodenta, Prospermophilus orientalis, Sinocricetus zdanskyi, Prosiphneus eriksoni, Pliosiphneus lyratus, Chardina n. sp.,C. sinensis, Pseudomeriones abbreviatus, Sicista sp., Apodemus sp., Hansdebruijnia pusillus, Chardinomys sp., and Allorattus sp. The beginning of biozone II is marked by the first appearance of Prosiphneus eriksoni in the depth of 59 m. Biozone III covers layers 15~17, ranges from the base of C3n.4n to the upper part of C3n.2n(Nunivak), and spans the time from 5.24 to 4.55 Ma. Fossils found in this biozone include Erinaceus sp., Parasoriculus sp., Ochotonoma n. sp.2, Ochotona minor,O. lingtaica, Trischizolagus mirificus, Sinotamias n. sp., Sinocricetus zdanskyi, Cricetinus mesolophidus, Mimomys teilhardi, Pliosiphneus lyratus, Chardina sinensis,C. truncatus, Mesosiphneus sp., Pseudomeriones abbreviatus,P. complicidens, Chardinomys sp,C. yusheensis, and Apodemus sp. The beginning of biozone III is marked by the first appearance of Mesosiphneus sp. at 35.5 m. Biozone IV covers layers 18~20, ranges from the upper part of C3n.2n to the top of the section, and has a time span from 4.55 to 3.5 Ma. The small mammals found in this biozone include Ochotonoma n. sp.2, Pliosiphneus lyratus, Mesosiphneus praetingi, Chardina truncatus, and Chardinomys nihowanicus. The first appearance of Mesosiphneus praetingi at the depth of 20.4 m marks the beginning of this biozone. Biozone I and II are correlated to the late Late Miocene, equivalent to Baodean, while biozone III and IV are correlated to the early Pliocene, equivalent to early Yushean. According to the paleomagnetic study, the boundary of Miocene/Pliocene (5.33 Ma) is located at the depth of 35.5 m of the section, and coincides with the last appearances of Prosiphneus eriksoni and Ochotonoma primitiva. The Miocene/Pliocene boundary is 2 meters lower than the boundary be-tween biozone II and III, which is marked by the earliest appearance of Mesosiphneus sp. Except Mesosiphneus sp., the earliest records of Paenepetenyia cf.P. zhudingi, Apodemus sp. And Ochotona lingtaica are also found closely above the boundary (1~2.5 meters). About 3 meters below the boundary, Parasoriculus sp., Sulimskia sp., Pliosiphneus lyratus, Chardina sinensis and Chardinomys sp. appear, and O. plicodenta and Sicista sp. disappear. The continuous sequence and high density of fossil levels qualify the section as a candidate stratotype section of Yushean Stage.
    EVOLUTION OF CRANIAL CAVITIES IN GIANT PANDAS (AILUROPODA, CARNIVORA, MAMMALIA)
    DONG Wei, ZHANG Jue-Fei
    2011, 49(2):  241-252. 
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    Three-dimensional virtual cranial endocasts of the Early Pleistocene Ailuropoda microta, the Late Pleistocene A. baconi, extant A. melanoleuca and Ursus maritimus were described and compared. The morphologies of cranial endocasts of giant pandas are generally similar to each other, but quite different from that of the polar bear. The intracranial volumes appear the smallest in A. microta, intermediate in A. melanoleuca, and the largest in A. baconi. The sulci and gyri impressions are developed on cranial endocasts of the giant pandas, more so in A. melanoleuca than in A. microta. On the contrary, they are not developed on the cranial endocast of the polar bear, but the blood vessel impressions are developed on the lateral occipital sides in the polar bears. The ventral longitudinal groove on olfactory endocast is developed in A. microta, weak in A. baconi, nearly absent in A.melanoleuca, but well developed in Ursus maritimus. The encephalization quotient is similar among A.microta, A. baconi and A. melanoleuca, but it is much greater for giant pandas than in the polar bear. The morphology of the paranasal sinuses is also similar among giant pandas, but different from that of the polar bear. The frontal sinuses of giant pandas are rather long, quite high and dorsally ridgy, but those of the polar bear are shorter, relatively lower, wider and dorsally flat. The maxillary sinuses of giant pandas are relatively wide, but those of the polar bear are narrow. The sphenoid sinuses of giant pandas are all small, but those of the polar bear are large and cover the anterior portion of the braincase. These endocranial differences between giant pandas and the polar bear support the classification of giant pandas as an independent family.