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内蒙古阿拉善左旗乌兰塔塔尔最晚始新世-渐新世剖面的区域年代地层意义

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  • 1 芬兰赫尔辛基大学地球科学与地理学系 赫尔辛基 00014
    2 中国科学院古脊椎动物与古人类研究所,中国科学院脊椎动物演化与人类起源重点实验室 北京 100044
    3 中国科学院生物演化与环境卓越创新中心 北京 100044
    4 中国科学院大学地球与行星科学学院 北京 100049

收稿日期: 2020-12-22

  网络出版日期: 2022-02-14

基金资助

芬兰科学院基金(编号)(316799);中国科学院战略性先导科技专项(编号)(XDB26000000);中国科学院古生物化石发掘与修理专项、国家自然科学基金(批准号)(41472003);GeoDoc和Waldemar von Frenckell基金资助

Stratigraphical significance of Ulantatal sequence

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  • 1 Department of Geosciences and Geography, University of Helsinki P.O. Box 64, Helsinki 00014, Finland
    2 Key Laboratory of Vertebrate Evolution and Human Origins of Chinese Academy of Sciences, Institute of Vertebrate Paleontology and Paleoanthropology, Chinese Academy of Sciences Beijing 100044, China
    3 CAS Center for Excellence in Life and Paleoenvironment Beijing 100044, China
    4 College of Earth and Planetary Sciences, University of Chinese Academy of Sciences Beijing 100049, China

Received date: 2020-12-22

  Online published: 2022-02-14

摘要

精确的区域年代地层框架是探究地质历史时期气候变化与动物群演化事件的基础。过去5000万年中亚洲地区发生的最明显陆地哺乳动物群转换事件可能发生在始新世-渐新世转折时期(约34 Ma)。然而由于缺乏连续的地层记录或者对经典哺乳动物化石地点的地层划分与对比存在较大争议,这一重要转折时期动物群的演变尚不明晰。内蒙古阿拉善左旗乌兰塔塔尔地区丰富的最晚始新世-渐新世(白音期、乌兰塔塔尔期与塔本布鲁克期)哺乳动物化石及连续的地层记录为建立该时段区域年代地层框架奠定了基础。基于岩石地层学、生物地层学以及磁性地层学研究结果,推荐将乌兰塔塔尔剖面作为渐新统乌兰塔塔尔阶的区域单位层型剖面。乌兰塔塔尔阶底界位于克克阿木剖面15.9 m处(33.89 Ma); 塔本布鲁克阶底界位于综合剖面98 m处(27.7 Ma), 对应古地磁极性年表的C9r, 以中华鼠兔Sinolagomys的最低出现为标志。

本文引用格式

Joonas Wasiljeff, 张兆群 . 内蒙古阿拉善左旗乌兰塔塔尔最晚始新世-渐新世剖面的区域年代地层意义[J]. 古脊椎动物学报, 2022 , 60(1) : 42 -53 . DOI: 10.19615/j.cnki.2096-9899.210716

Abstract

Robust regional chronostratigraphic framework is the basis of understanding climatic and faunal events in the geologic history. One of the most dramatic faunal turnovers of the past 50 million years in Asia is linked to the Eocene-Oligocene Transition (EOT) at about 34 Ma. However, the chronostratigraphic relationships between faunal modulation and geologic events associated with the EOT in China have remained uncertain before and after the epoch boundaries, mainly due to the scarcity of continuous records and problems in correlating and subdividing the classic areas containing abundant mammalian fossils. Past decades have seen developments in establishing Chinese regional Paleogene Land Mammal Ages, and albeit many ages are well constrained, some, such as those of the latest Eocene and the Oligocene, have remained unsettled. In this paper, we present how recent evidence from the fossiliferous Ulantatal sequence, Nei Mongol, China, provides better constraints to the latest Eocene and Oligocene Chinese Land Mammal ages (Baiyinian, Ulantatalian, and Tabenbulukian). We propose Ulantatal sequence as a new regional unit stratotype section of the Ulantatalian stage, and the lower boundary of Tabenbulukian stage to be reassigned to Chron C9r (27.7 Ma), with the lowest occurrence of Sinolagomys as the marker horizon.

参考文献

[1] Coccioni R, Montanari A, Bice D et al., 2018. The Global Stratotype Section and Point (GSSP) for the base of the Chattian Stage (Paleogene System, Oligocene Series) at Monte Cagnero, Italy. Episodes, 41(1):13-32
[2] Daxner-H?ck G, Badamgarav D, Barsbold R et al., 2017. Oligocene stratigraphy across the Eocene and Miocene boundaries in the Valley of Lakes (Mongolia). Palaeobiodiv Palaeoenv, 97(1):111-218
[3] Dupont-Nivet G, Krijgsman W, Langereis C et al., 2007. Tibetan plateau aridification linked to global cooling at the Eocene-Oligocene transition. Nature, 445:635-638
[4] Eldrett J S, Greenwood D R, Harding I C et al., 2009. Increased seasonality through the Eocene to Oligocene transition in northern high latitudes. Nature, 459:969-973
[5] Gomes Rodrigues H, Marivaux L, Vianey-Liaud M, 2014. Rodent paleocommunities from the Oligocene of Ulantatal (Inner Mongolia, China). Paleovertebrata, 38(1): e3 (1-11)
[6] Hooker J J, Collinson M E, Sille N P, 2004. Eocene-Oligocene mammalian faunal turnover in the Hampshire Basin, UK: calibration to the global time scale and the major cooling event. J Geol Soc, 161(2):161-172
[7] Hren M T, Sheldon N D, Grimes S T et al., 2013. Terrestrial cooling in northern Europe during the Eocene-Oligocene transition. Proc Nat Acad Sci, 110:7562-7567
[8] Huang X S, 1982. Preliminary observations on the Oligocene deposits and mammalian fauna from Alashan Zuoqi, Nei Mongol. Vert PalAsiat, 20(4):337-349
[9] Kraatz B P, Geisler J H, 2010. Eocene-Oligocene transition in Central Asia and its effects on mammalian evolution. Geology, 38(2):111-114, doi: 10.1130/G30619.1
[10] Li C K, Ting S Y, 1983. The Paleogene mammals of China. Bull Carnegie Mus Nat Hist, 21:1-93
[11] Li Q, Meng J, Wang Y Q, 2016. New cricetid rodents from strata near the Eocene-Oligocene boundary in Erden Obo Section (Nei Mongol, China). PLoS ONE, 11(5): e0156233
[12] Li Q, Gong Y X, Wang Y Q, 2017. New dipodid rodents from the Late Eocene of Erden Obo (Nei Mongol, China). Hist Biol, 29(5):692-703
[13] Meng J, McKenna M C, 1998. Faunal turnovers of Palaeogene mammals from the Mongolian Plateau. Nature, 394:364-367
[14] Pound M J, Salzmann U, 2017. Heterogeneity in global vegetation and terrestrial climate change during the Late Eocene to Early Oligocene transition. Sci Rep, 7:43386
[15] Premoli Silva I, Jenkins D G, 1993. Decision on the Eocene-Oligocene boundary stratotype. Episodes, 16(3):379-382
[16] Prothero D R, Heaton T, 1996. Faunal stability during the Early Oligocene climatic crash. Palaeogeogr Palaeoclimatol Palaeoecol, 127(1-4):257-283
[17] Qiu Z X, Wang B Y, Qiu Z D et al., 1997. Recent advances in study of the Xianshuihe Formation in Lanzhou basin. In: Tong Y S, Zhang Y Y, Wu W Y et al. eds. Evidence for Evolution-Essays in Hornor of Prof. Chunchien Young on the Hundredth Anniversary of His Birth. Beijing: China Ocean Press. 177-192
[18] Qiu Z X, Qiu Z D, Deng T et al., 2013. Neogene land mammal stages/ages of China. In: Wang X M, Flynn L J, Fortelius M eds. Fossil Mammals of Asia: Neogene Biostratigraphy and Chronology. New York: Columbia University Press. 29-90
[19] Romer A S, 1966. Vertebrate Paleontology. Chicago and London: University of Chicago Press. 1-467
[20] Russell D E, Zhai R J, 1987. The Paleogene of Asia: mammals and stratigraphy. Mem Mus Natl His Nat, Ser C, 52:1-488
[21] Speijer R P, P?like H, Hollis C J et al., 2020. The Paleogene Period. In: Gradstein F M, Ogg J G, Schmitz M D et al. eds. The Geologic Time Scale 2020. Oxford: Elsevier BV. 1087-1140
[22] Sun J M, Ni X J, Bi S D et al., 2014. Synchronous turnover of flora, fauna, and climate at the Eocene-Oligocene boundary in Asia. Sci Rep, 4:7463
[23] Tertiary Research Group of Chinese National Petroleum Corporation, 1991. Correlation of the Tertiary in Chinese oil and gas zones with European and American Standard Sequence. Chinese Sci Bull, 19:1494-1495
[24] Tong Y S, Zheng S H, Qiu Z D, 1995. Cenozoic mammal ages of China. Vert PalAsiat, 33(4):290-314
[25] Vianey-Liaud M, Schmidt-Kittler N, Marivaux L, 2006. The Ctenodactylidae (Rodentia) from the Oligocene of Ulantatal (Inner Mongolia, China). Paleovertebrata, 34(3-4):111-205
[26] Wang B Y, 1992. The Chinese Oligocene: a preliminary review of mammalian localities and local fauna. In: Prothero D R, Berggren W A eds. Eocene-Oligocene Climate and Biotic Evolution. Oxford: Princeton University Press. 529-547
[27] Wang B Y, 1997a. Chronological sequence and subdivision of Chinese Oligocene mammalian faunas. J Stratigr, 21:183-191
[28] Wang B Y, 1997b. Problems and recent advances in the division of the continental Oligocene. J Stratigr, 21:81-90
[29] Wang B Y, Wang P Y, 1991. Discovery of early medial Oligocene mammalian fauna from Kekeamu, Alxa Left Banner, Nei Mongol. Vert PalAsiat, 29(1):64-71
[30] Wang X M, Wang B Y, Qiu Z X et al., 2003. Danghe area (western Gansu, China) biostratigraphy and implications for depositional history and tectonics of northern Tibetan Plateau. Earth Planet Sci Lett, 208:253-269
[31] Wang X M, Wang B Y, Qiu Z X, 2008. Early explorations of the Tabenbuluk region (western Gansu Province) by Birger Bohlin - Reconciling classic vertebrate fossil localities with modern stratigraphy. Vert PalAsiat, 46(1):1-19
[32] Wang Y Q, Meng J, Ni X J et al., 2007. Major events of Paleogene mammal radiation in China. Geol J, 42:415-430
[33] Wang Y Q, Meng J, Jin X, 2012. Comments on Paleogene localities and stratigraphy in the Erlian Basin, Nei Mongol, China. Vert PalAsiat, 50(3):181-203
[34] Wang Y Q, Li Q, Bai B et al., 2019. Paleogene integrative stratigraphy and timescale of China. Sci China Earth Sci, 62(1):287-309, doi: 10.1007/s11430-018-9305-y
[35] Wasiljeff J, Kaakinen A, Salminen J et al., 2020. Magnetostratigraphic constraints on the fossiliferous Ulantatal sequence in Inner Mongolia, China: implications for Asian aridification and faunal turnover before the Eocene-Oligocene boundary. Earth Planet Sci Lett, 535:116125, doi: 10.1016/j.epsl.2020.116125
[36] Yue L P, Heller F, Qiu Z X et al., 2001. Magnetostratigraphy and pavleo-environmental record of Tertiary deposits of Lanzhou Basin. Chinese Sci Bull, 46(1):770-773
[37] Zachos J, Pagani M, Sloan L et al., 2001. Trends, rhythms, and aberrations in global climate 65 Ma to present. Science, 292:686-693
[38] Zhang Z Q, Liu Y, Wang L H et al., 2016. Lithostratigraphic context of Oligocene mammalian faunas from Ulantatal, Nei Mongol, China. C R Palevol, 15(7):903-910
[39] Zhang R, Kravchinsky V A, Yue L P, 2012. Link between global cooling and mammalian transformation across the Eocene-Oligocene boundary in the continental interior of Asia. Int J Earth Sci, 101(8):2193-2200
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