PDF File Includes: Supplementary Text Figs

Total Page:16

File Type:pdf, Size:1020Kb

PDF File Includes: Supplementary Text Figs Supplementary Information for Title: When did Homo sapiens first reach Southeast Asia and Sahul? Authors: James F O’Connell, Jim Allen, Martin AJ Williams, Alan N Williams, Chris SM Turney, Nigel A Spooner, Johan Kamminga, Graham Brown, Alan Cooper Corresponding author: James F O’Connell Email: [email protected] This PDF file includes: Supplementary text Figs. S1 to S4 Table S1 References for SI reference citations Supplementary Information SI.1 Hominin fossils SI.1.1 – Background notes Four species of Homo are identified on the South China-Sahul arc (1). Defining characteristics include aspects of body size, skeletal robusticity, and cranial anatomy. H. erectus (2,3). This is a widespread taxon, known from parts of Africa, Europe, North China, and Java, and dated from 1.8 Ma to the late Middle Pleistocene (<200 ka). Postcranial anatomy is relatively robust; estimated height and weight are within the modern human range. Crania are defined by a low vault, receding frontal, prominent brow ridges, moderate post-orbital constriction, and occipital angulation. Brain sizes are estimated at 700-1200 cc. Examples from Java are well represented in deposits dating 500-1000 ka. Some may have been present there as early as 1.6 Ma (4,5). Terminal dates as recent as 143 ka are cited for Javanese populations (6). Persistence to the time of anatomically modern human (AMH) arrival is possible but disputed (7,8). Skeletal and archaeological evidence indicates a presence on Flores >1.0 Ma (9,10); archaeological evidence suggests the same on Sulawesi >200 ka (11). Other interpretations, one involving Denisovans on Sulawesi, are also plausible (12). H. floresiensis (13). This is an insular dwarf known from deposits on Flores dated 60-100 ka (13,14). Brain size is estimated at c. 425 cc.; height 100-109 cm; weight 30-41 kg. Appendicular proportions differ significantly from those of H. erectus and later humans. Homo sp. teeth from c. 0.7 Ma, also on Flores, are similar in form and size to those of H. floresiensis, suggesting long- term taxonomic and locational continuity (10). Derivation is attributed to early H. erectus (10,15) or H. habilis (16,17), the former being more parsimonious. The >66 ka metatarsal from Callao, assigned to Homo sp. and widely referenced as a small-bodied H. sapiens, might represent H. floresiensis or a similarly dwarfed insular collateral (18). Archaic H. sapiens (19-21). Fossils assigned to this category are also called Late H. erectus, H. heidelbergensis, or pre-modern H. sapiens. They combine H. erectus-like features, including a 1 www .pnas.org/cgi/doi/10.1073/pnas.1808385115 massive, forwardly projecting supraorbital torus, thick cranial walls, and great basal breadth, with derived traits, including an endocranial capacity of >1200 cc, a relatively steep (non- receding) frontal, and a relatively rounded occipital. Dated East Asian specimens are Late Middle Pleistocene in age, roughly 100-400 ka. It is uncertain whether they reflect an in situ evolution of Asian H. erectus or are the product of Middle Pleistocene (>400 ka) introgression with African or European H. heidelbergensis (22). They may represent Denisovans (23). Examples are reported from China and SE Asia (e.g. Dali, Jinniushan, Maba [19]; more recently Xuchang [22]) but are so far not known from Sunda or areas further east. H. sapiens (24). Also called anatomically modern humans (AMH). Some characteristic attributes are known from Africa by 160-195 ka (25,26) and are recently reported there as early as 300 ka (27). A broader list of attributes are known from Southwest Asia at 100-130 ka (28,29) and are recently reported there as early as 177-194 ka (30). Strictly defined, AMH are identified in Africa before 50 ka, are widespread across the Eastern Hemisphere after 50 ka, and present in the Americas after 15 ka (31). They are identified by a high, rounded neurocranium, basicranial flexion, small face retracted under the frontal bone, true chin, and small, discontinuous brow ridges. Early East and Southeast Asian and Australasian examples include Tam Pà Ling (TPL 1, Laos), Niah Deep Skull (Borneo), and WLH 1, 3 (Australia). They may date earlier in South China and Southeast Asia but that is uncertain (see below). SI.1.2 - SCS arc fossils, dated 40-120 ka, said by some to represent H. sapiens SI.1.2.1 China Bailian (32). Published in Chinese, with English abstract. Two hominin teeth identified as H. sapiens; overlain by flowstone dated 160 ka via U-series. Dennell (1) is skeptical of both the identification as H. sapiens and the estimated age. Fuyan (33,34). Forty-seven teeth, dated 80-120 ka, said to be “more derived than any other anatomically modern humans, resembling middle-to-late Late Pleistocene specimens and even contemporary humans” (33). Specimens were recovered from a sandy clay (Layer 2) associated with remains of a Late Pleistocene fauna, some elements of which are extinct. U-series dates on eight speleothem fragments in the same layer range from 120-557 ka. One non-human bone from the same layer yielded a calibrated radiocarbon date of 42-43 ka. A stalagmite purportedly rooted in overlying Layer 1 yielded two U-series dates, said to indicate a minimum age of 80 ka for the underlying component and its contents. Liu et al. (33) reject the 14C date, citing technical limits of the laboratory that provided it. They favor the 120 ka U-series speleothem determination over the seven others and conclude that the human teeth in Layer 2 fall in the range 80-120 ka. Michel et al. (34) observe that the Layer 2 sediments are “suggestive of extensive fluvial activity … which raises the possibility that the deposits are reworked and actually comprise materials from different time periods.” The 42-43 ka radiocarbon date, the wide range of associated speleothem dates, and the derived quality of the teeth are consistent with this possibility. Michel et al. question whether the stalagmite from Layer 1 actually pertains to that component, rather than to underlying Layer 2. They also note that it is at least 15m away from any of the teeth, raising further questions about its relationship with the latter. They regard as inadequate 2 the appeal to faunal correlations as an additional basis for the 80-120 ka age-estimate. They conclude that the teeth may date from “the latter half of the Late Pleistocene or even more recently.” Ganquian (Tubo) (35). Published in Chinese, with English abstract. Seventeen hominin teeth identified as H. sapiens; bracketed by flowstone layers dated 94-220 ka via U-series. Dennell (1) accepts an age estimate of c. 100 ka but is skeptical of assignment of the teeth to H. sapiens. Huanglong (36,37). Sample includes seven human teeth from multiple individuals. Comparative analysis (36) shows that most of their morphological and metric features resemble those of modern H. sapiens: “Generally speaking, the Huanglong Cave human teeth look gracile and lack the archaic features usually identified on Middle and Late Pleistocene humans. [This] study also indicates that the Huanglong Cave human teeth already possess some dental features of modern East Asian populations.” The teeth were recovered from the lower portion of a red silty clay (Layer 3) in association with stone artifacts, non-human faunal remains, and dark, carbon-rich patches read as the remains of anthropogenic fires. Liu et al. (36) appeal to sediment clast size, lack of evidence of bone or artifact rounding, and the presence of the carbon patches as evidence that Layer 3 contents including human teeth are in primary context, not re-deposited from another location. Layer 3 dates originally reported from rhinoceros teeth (U-series 79.4 ± 6.3 ka, 94.7 ± 12.5 ka; ESR 34-44 ka) and a stalagmite (U-series, c. 103 ka) were seen as potentially unreliable (36,37), the former for methodological reasons, the latter because of uncertainty about sample provenience relative to the human teeth. Subsequent U-series analyses of the thin, patchily distributed flowstone capping Layer 3 yielded a date of 28 ka. Flowstones in the upper part of Layer 3 were pegged at 32-45 ka; those in the mid-lower part of Layer 3 at a composite 81.4 ± 1.1 ka. The latter estimate is seen by Liu et al. (36) as a minimum date for the human teeth. The weighted mean of three samples underlying the teeth is 101 ± 1, indicating a maximum age for the teeth; hence, the bracketing age estimate of 81-101 ka. Bae (38) is cautious about whether teeth are in primary context, citing possible fluvial or rodent disturbance. Dennell (1) expresses similar concerns. As at Fuyan, the derived quality of the teeth encourages this skepticism. Laibin (Gaitou) (39,40). The term Laibin applies to a set of hominin remains collected from Gaitou Cave in 1956. They consist of three disconnected pieces, probably once part of the same individual, including “a nearly complete hard palate with several teeth and the adjoining lower part of the body of the maxilla, a large part of the right zygomatic, and an occipital fragment” (40). They were identified by Jia and Wu (39) as H. sapiens based on a “lack of distinct archaic features.” Dennell (1) favors a date of 39-44 ka. All skeletal parts were recovered from a sandy clay layer, capped by a thick flowstone. Two U- series dates on that flowstone have a weighted mean of 38.5 ± 1.0 ka. Two dates on thinner, less extensive flowstones within the sandy clay, said to underlie sediments where the fossils were located, have a weighted mean of 44.0 ± 0.8 ka.
Recommended publications
  • Discovery of the Fuyan Teeth: Challenging Or Complementing the Out-Of-Africa Scenario?
    ZOOLOGICAL RESEARCH Discovery of the Fuyan teeth: challenging or complementing the out-of-Africa scenario? Yu-Chun LI, Jiao-Yang TIAN, Qing-Peng KONG Although it is widely accepted that modern humans (Homo route about 40-60 kya (Macaulay et al, 2005; Sun et al, 2006). sapiens sapiens) can trace their African origins to 150-200 kilo The lack of human fossils dating earlier than 70 kya in eastern years ago (kya) (recent African origin model; Henn et al, 2012; Eurasia implies that the out-of-Africa immigrants around 100 Ingman et al, 2000; Poznik et al, 2013; Weaver, 2012), an kya likely failed to expand further east (Shea, 2008). Consistent alternative model suggests that the diverse populations of our with this notion, the Late Pleistocene hominid records species evolved separately on different continents from archaic previously found in eastern Eurasia have been dated to only human forms (multiregional origin model; Wolpoff et al, 2000; 40-70 kya, including the Liujiang man (67 kya; Shen et al, 2002) Wu, 2006). The recent discovery of 47 teeth from a Fuyan cave and Tianyuan man (40 kya; Fu et al, 2013b; Shang et al, 2007) in southern China (Liu et al, 2015) indicated the presence of H. in China, the Mungo Man in Australia (40-60 kya; Bowler et al, s. sapiens in eastern Eurasia during the early Late Pleistocene. 1972), the Niah Cave skull from Borneo (40 kya; Barker et al, Since the age of the Fuyan teeth (80-120 kya) predates the 2007) and the Tam Pa Ling cave man in Laos (46-51 kya; previously assumed out-of-Africa exodus (60 kya) by at least 20 Demeter et al, 2012).
    [Show full text]
  • Establishing Robust Chronologies for Models of Modern Human
    Establishing robust chronologies for models of modern human dispersal in Southeast Asia; implications for arrival and occupation in Sunda and Sahul A thesis submitted in fulfilment of the requirements for the award of the degree Masters of Research from MACQUARIE UNIVERSITY by Lani M. Barnes BSc. Macquarie University Department of Environment and Geography 10 October 2014 1 Table of Contents ABSTRACT I DECLARATION II ACKNOWLEDGEMENTS III LIST OF FIGURES IV LIST OF TABLES VI LIST OF ABBREVIATIONS AND SYMBOLS VII CHAPTER 1: INTRODUCTION 1 1.1 AIMS AND OBJECTIVES 3 1.2 OUTLINE 3 CHAPTER 2: ESTABLISHING MODERN HUMAN PRESENCE IN MAINLAND SOUTHEAST ASIA; THE NEED FOR ROBUST CHRONOLOGIES 4 SECTION I: CURRENT MODELS OF MODERN HUMAN DISPERSAL AND THE PALEOANTHROPOLOGICAL AND ARCHAEOLOGICAL RECORD 4 2.1 INTRODUCTION 4 2.2 THE START AND END OF OUT OF AFRICA 2 4 2.3 MIS4-3 RAPID COASTAL DISPERSAL 5 2.4 MODERN HUMAN EVIDENCE IN SUNDA AND SAHUL 7 2.5 THE CONTRIBUTION OF MIDDLE PALAEOLITHIC TECHNOLOGIES TO UNDERSTANDING THE COMPLEXITIES REGARDING MODELS OF MODERN HUMAN DISPERSAL 9 SECTION II: CHRONOMETRIC TECHNIQUES AVAILABLE TO ESTABLISH ROBUST CHRONOLOGIES FOR MODERN HUMAN PALEOANTHROPOLOGICAL AND ARCHAEOLOGICAL EVIDENCE 12 2.6 INTRODUCTION 12 2.7 URANIUM-THORIUM (U-TH) DATING 12 2.8 LUMINESCENCE DATING 14 2.9 RADIOCARBON DATING 17 2.10 IMPLICATIONS FOR RESEARCH IN MAINLAND SOUTHEAST ASIA 18 CHAPTER 3: BUILDING FROM PREVIOUS RESEARCH AT THE SITES OF TAM PA LING, NAM LOT AND THAM LOD TO ESTABLISH ROBUST CHRONOLOGIES 20 3.1 TAM HANG CAVES LAOS 20 3.1.1
    [Show full text]
  • Supplementary Information For
    Supplementary Information for An Abundance of Developmental Anomalies and Abnormalities in Pleistocene People Erik Trinkaus Department of Anthropology, Washington University, Saint Louis MO 63130 Corresponding author: Erik Trinkaus Email: [email protected] This PDF file includes: Supplementary text Figures S1 to S57 Table S1 References 1 to 421 for SI reference citations Introduction Although they have been considered to be an inconvenience for the morphological analysis of human paleontological remains, it has become appreciated that various pathological lesions and other abnormalities or rare variants in human fossil remains might provide insights into Pleistocene human biology and behavior (following similar trends in Holocene bioarcheology). In this context, even though there were earlier paleopathological assessments in monographic treatments of human remains (e.g., 1-3), it has become common to provide details on abnormalities in primary descriptions of human fossils (e.g., 4-12), as well as assessments of specific lesions on known and novel remains [see references in Wu et al. (13, 14) and below]. These works have been joined by doctoral dissertation assessments of patterns of Pleistocene human lesions (e.g., 15-18). The paleopathological attention has been primarily on the documentation and differential diagnosis of the abnormalities of individual fossil remains, leading to the growing paleopathological literature on Pleistocene specimens and their lesions. There have been some considerations of the overall patterns of the lesions, but those assessments have been concerned primarily with non-specific stress indicators and traumatic lesions (e.g., 13, 15, 19-21), with variable considerations of issues of survival 1 w ww.pnas.org/cgi/doi/10.1073/pnas.1814989115 and especially the inferred social support of the afflicted (e.g., 22-27).
    [Show full text]
  • Ancient DNA and Multimethod Dating Confirm the Late Arrival of Anatomically Modern Humans in Southern China
    Ancient DNA and multimethod dating confirm the late arrival of anatomically modern humans in southern China Xue-feng Suna,1,2, Shao-qing Wenb,1, Cheng-qiu Luc, Bo-yan Zhoub, Darren Curnoed,2, Hua-yu Lua, Hong-chun Lie, Wei Wangf, Hai Chengg, Shuang-wen Yia, Xin Jiah, Pan-xin Dub, Xing-hua Xua, Yi-ming Lua, Ying Lua, Hong-xiang Zheng (郑鸿翔)b, Hong Zhangb, Chang Sunb, Lan-hai Weib, Fei Hani, Juan Huangj, R. Lawrence Edwardsk, Li Jinb, and Hui Li (李辉)b,l,2 aSchool of Geography and Ocean Science, Nanjing University, 210023 Nanjing, China; bSchool of Life Sciences & Institute of Archaeological Science, Fudan University, Shanghai 200438, China; cHubei Provincial Institute of Cultural Relics and Archeology, 430077 Wuhan, China; dAustralian Museum Research Institute, Australian Museum, Sydney, NSW 2010, Australia; eDepartment of Geosciences, National Taiwan University, 106 Taipei, Taiwan; fInstitute of Cultural Heritage, Shandong University, 266237 Qingdao, China; gInstitute of Global Environmental Change, Xi’an Jiaotong University, 710049 Xi’an, China; hSchool of Geography Science, Nanjing Normal University, 210023 Nanjing, China; iResearch Centre for Earth System Science, Yunnan University, 650500 Kunming, China; jCultural Relics Administration of Daoxian County, Daoxian 425300, China; kDepartment of Geology and Geophysics, University of Minnesota, Minneapolis, MN 55455; and lFudan-Datong Institute of Chinese Origin, Shanxi Academy of Advanced Research and Innovation, 037006 Datong, China Edited by Richard G. Klein, Stanford University, Stanford, CA, and approved November 13, 2020 (received for review September 10, 2020) The expansion of anatomically modern humans (AMHs) from year before present, i.e., before AD1950) Ust’-Ishim femur Africa around 65,000 to 45,000 y ago (ca.
    [Show full text]
  • A Late Middle Pleistocene Denisovan Mandible from the Tibetan Plateau
    Kent Academic Repository Full text document (pdf) Citation for published version Chen, Fahu and Welker, Frido and Shen, Chuan-Chou and Bailey, Shara E. and Bergmann, Inga and Davis, Simon and Xia, Huan and Wang, Hui and Fischer, Roman and Freidline, Sarah E. and Yu, Tsai-Luen and Skinner, Matthew M. and Stelzer, Stefanie and Dong, Guangrong and Fu, Qiaomei and Dong, Guanghui and Wang, Jian and Zhang, Dongju and Hublin, Jean-Jacques DOI https://doi.org/10.1038/s41586-019-1139-x Link to record in KAR https://kar.kent.ac.uk/74280/ Document Version Author's Accepted Manuscript Copyright & reuse Content in the Kent Academic Repository is made available for research purposes. Unless otherwise stated all content is protected by copyright and in the absence of an open licence (eg Creative Commons), permissions for further reuse of content should be sought from the publisher, author or other copyright holder. Versions of research The version in the Kent Academic Repository may differ from the final published version. Users are advised to check http://kar.kent.ac.uk for the status of the paper. Users should always cite the published version of record. Enquiries For any further enquiries regarding the licence status of this document, please contact: [email protected] If you believe this document infringes copyright then please contact the KAR admin team with the take-down information provided at http://kar.kent.ac.uk/contact.html A late Middle Pleistocene Denisovan mandible from the Tibetan Plateau Fahu Chen1,2§*, Frido Welker3,4§, Chuan-Chou Shen5,6§, Shara E.
    [Show full text]
  • The Origin of Modern East Asians
    第 32 卷,第 4 期 人 类 学 学 报 Vol.32, No.4 2013 年 11 月 ACTA ANTHROPOLOGICA SINICA November, 2013 The Origin of Modern East Asians Milford H Wolpoff 1, Rachel Caspari 2 1. Department of Anthropology, University of Michigan, Ann Arbor, MI 48109, USA,E-mail: [email protected] 2. Department Sociology, Anthropology, and Social Work, Central Michigan University, Mount Pleasant, MI 48859, USA Abstract: With the development of paleogenetics in the past decade, it has become evident that modern humans do not have a phylogenetic origin in the appearance of a new species Homo sapiens; therefore, anatomical, behavioral and genetic aspects of modernity are not the consequence of the same, single event. In this paper, we examine the evidence for anatomical, behavioral and genetic modernity in East Asia. In each case, modernity can be understood as part of a multiregional evolutionary process, rather than as an entity. Although these three aspects of modernity are somewhat independent, each evolving at different times, they are linked through demographic changes that began in the late Pleistocene - increased survivorship and population expansions that changed the course of human evolution. Key words: Asian Evolution, Modernity Chinese Library Classification: Q981; Document Code: A; No:1000-3193(2013)04-0377-34 1 The pattern of human evolution The human lineage originated in Africa, near the end of the Pliocene. The time of origin of this lineage, the unique ancestors of recent and living human populations, is defined by when it became distinct from other australopithecine lineages. Some researchers regard the lineage as synonymous with the human species itself, Homo sapiens[1, 2], using a phylogenetic definition[3] of Homo sapiens, rather than an anatomical one.
    [Show full text]
  • Current Anthropology
    Forthcoming Current Anthropology Wenner-Gren Symposium Current Anthropology Supplementary Issues (in order of appearance) Current VOLUME 58 SUPPLEMENT 17 DECEMBER 2017 The Anthropology of Corruption. Sarah Muir and Akhil Gupta, eds. Cultures of Militarism. Catherine Besteman and Hugh Gusterson, eds. Patchy Anthropocene. Anna Tsing, Nils Bubandt, and Andrew Mathews, eds. Anthropology Previously Published Supplementary Issues Engaged Anthropology: Diversity and Dilemmas. Setha M. Low and Sally Engle Merry, eds. THE WENNER-GREN SYMPOSIUM SERIES Corporate Lives: New Perspectives on the Social Life of the Corporate Form. December 2017 Damani Partridge, Marina Welker, and Rebecca Hardin, eds. The Origins of Agriculture: New Data, New Ideas. T. Douglas Price and HUMAN COLONIZATION OF ASIA IN THE LATE PLEISTOCENE Ofer Bar-Yosef, eds. GUEST EDITORS: CHRISTOPHER J. BAE, KATERINA DOUKA, The Biological Anthropology of Living Human Populations: World Histories, AND MICHAEL D. PETRAGLIA National Styles, and International Networks. Susan Lindee and Ricardo Ventura Santos, eds. Human Colonization of Asia in the Late Pleistocene Human Biology and the Origins of Homo. Susan Antón and Leslie C. Aiello, eds. Human Colonization of Asia in the Late Pleistocene: The History of an Invasive Species Potentiality and Humanness: Revisiting the Anthropological Object in 58 Volume A Genomic View of the Pleistocene Population History of Asia Contemporary Biomedicine. Klaus Hoeyer and Karen-Sue Taussig, eds. Testing Modern Human Out-of-Africa Dispersal Models Using Dental Nonmetric Data Alternative Pathways to Complexity: Evolutionary Trajectories in the Middle Archaic Hominin Populations in Asia before the Arrival of Modern Humans: Their Paleolithic and Middle Stone Age. Steven L. Kuhn and Erella Hovers, eds.
    [Show full text]
  • How Old Are the Oldest Homo Sapiens in Far East Asia?
    COMMENTARY How old are the oldest Homo sapiens in Far East Asia? COMMENTARY Jean-Jacques Hublina,b,1 There is abundant genetic and paleontological evi- cultural, and demographic changes made groups of dence supporting the African origin of our species. At hunter-gatherers of African origins able to colonize some point in its evolution, Homo sapiens spread out totally new environments at the expense of local ar- of Africa into Eurasia, replacing or partially absorbing chaic groups. In the midlatitudes, they were already local populations of other hominin forms. Ultimately, it present before 45,000 y ago in eastern Europe (6). colonized regions where no humans had ever lived They also rapidly expanded eastward up to 57° north- before. Although extant humans display some physi- ern latitude in Siberia (7), and along a “northern route” cal variations resulting from adaptation to local condi- avoiding the Himalayan range, they may have reached tions and isolation, they all share a recent African Mongolia and northern China (8). ancestry. How many times, when, and why this dis- In the south, the central issue is whether the expan- persal out of Africa occurred have been a matter of sion of our species across tropical Asia was just the continuous debate in the field of paleoanthropology. continuation of its early arrival in southwest Asia or In the past decade, research efforts have intensified in resulted from a much later phase of dispersal along a Far East Asia to elucidate the timing of the arrival of so-called “southern route.” Unfortunately, with the our species and have produced several notable pub- noticeable exceptions of China and Java Island, the lications.
    [Show full text]
  • Human Colonization of Asia in the Late Pleistocene an Introduction to Supplement 17
    Current Anthropology Volume 58, Supplement 17, December 2017 S000 Human Colonization of Asia in the Late Pleistocene An Introduction to Supplement 17 by Christopher J. Bae, Katerina Douka, and Michael D. Petraglia The origin and evolution of modern humans continues to be of great interest to the scientific and public communities alike; the field has long been dominated by findings from Europe and Africa. With new discoveries of hominin fossils and archaeological sites, in addition to the application of recent genomic and paleoclimate modeling studies, findings from Asia are serving to revolutionize the field of modern human origins. The identification of Neanderthals and Denisovans in Siberia, for example, along with growing fossil and archaeological evidence for the presence of early modern humans in East and Southeast Asia, much earlier than originally thought, places the spotlight on the evolu- tionary history of our species in Asia over the last 125,000 years. Exciting and unanticipated new discoveries call for a need to critically reexamine the Asian record. Taking a multidisciplinary perspective, a group of active researchers participated in a week-long Wenner-Gren symposium titled “Human Colonization of Asia in the Late Pleistocene” (#153) in March 2016. Here we review the major themes and findings emerging from the symposium and discuss avenues to move the field forward. Background altitudinal breadth covers a great range of environments, includ- ing tropical forests, deserts, steppes, permafrost zones, and even fi fi Signi cant paleoanthropological ndings routinely are reported open seas and oceans. Major riverways (e.g., Indus, Irrawaddy, from Europe and Africa owing to prolonged and large-scale Yangtze) connect different biomes and would have thus facili- research campaigns on the part of multidisciplinary teams.
    [Show full text]
  • Diet of the Earliest Modern Humans in East Asia
    Diet of the earliest modern humans in East Asia Yan Wu ( [email protected] ) Chinese Academy of Sciences Dawei Tao Department of Archaeology, School of History, Zhengzhou University https://orcid.org/0000-0003- 1836-4390 Xiujie Wu Institute of Vertebrate Paleontology and Paleoanthropology, Chinese Academy of Sciences Wu Liu Institute of Vertebrate Paleontology and Paleoanthropology, Chinese Academy of Sciences Article Keywords: Hominins, Diet, Starch analysis, Dental calculus, Plants Posted Date: May 7th, 2021 DOI: https://doi.org/10.21203/rs.3.rs-442096/v1 License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License Page 1/15 Abstract Reconstructing diet can offer an improved understanding of the origin and evolution of modern humans. However, the diet of early modern humans in East Asia is poorly understood. Starch analysis of dental calculus is harmless to precious fossil hominins and provides the most direct evidence of plant food sources in early modern human dietary records. In this paper, we examined starch grains in dental calculus from Fuyan Cave hominins in Daoxian (South China), which were the earliest modern humans in East Asia. Our results reveal the earliest direct evidence of a hominin diet made of acorns, roots, tubers, grass seeds, and other yet-unidentied plants in marine isotope stage 5 between 120–80 ka. Our study also provides the earliest evidence that acorns may have played an important role in subsistence strategies. There may have been a long-lasting tradition of using these plants during the Late Pleistocene in China. Plant foods would have been a plentiful source of carbohydrates that greatly increased energy availability to human tissues with high glucose demands, such as the brain, red blood cells, and developing fetuses.
    [Show full text]
  • Human Remains from Zhirendong, South China, and Modern Human Emergence in Eastern Asia Supporting Information
    Human Remains from Zhirendong, South China, and Modern Human Emergence in Eastern Asia Supporting Information Wu Liu, Chang-Zhu Jin, Ying-Qi Zhang, Yan-Jun Cai, Song Xing, Xiu-Jie Wu, Hai Cheng, R. Lawrence Edwards, Wen-Shi Pan, Da-Gong Qin, Zhi-Sheng An, Erik Trinkaus and Xin-Zhi Wu I. Zhirendong (Zhiren Cave) Figure S1. Map of eastern Asia with the locations of Zhirendong and other sites which have yielded late archaic or early modern human remains, in China unless otherwise specified. A: late archaic; M: early modern. Star: Zhirendong (Zhiren Cave); 1: Zhoukoudian-Upper Cave (M); 2: Xujiayao (M); 3: Salawusu (M); 4: Huanglong (M); 5: Ziyang (M); 6: Lijiang (M); 7: Liujiang (M); 8: Maba (A); 9: Okinawan sites of Yamashita-cho, Pinza-Abu and Minatogawa (M); 10: Salkhit, Mongolia (A); 11: Malta, Siberia (M); 12: Altai sites of Denisova and Okladnikov Caves (A); 13: Niah Cave, Sarawak (M); 14: Moh Khiew, Thailand (M); 15: Fa Hien and Batadomba lena, Sri Lanka (M) Figure S2. View of the Mulanshan (Mulan Mountain) across the modern land surface, with the location of Zhirendong (Zhiren Cave; ZRD). The Hejiang River curves around the base of the mountain below the cave. Figure S3. Plan of Zhirendong (Zhiren Cave). The gray area indicates the excavated area. Modified from Jin et al. (1). 2 Figure S4. Post-excavation views of Zhirendong (Zhiren Cave). Left: the main entrance area to the cave; the excavated area is to the left beyond the individuals standing within the cave. Right: the main excavation trench in the lower portion of Section B of the stratigraphy, with the exploratory well evident within the trench.
    [Show full text]
  • Human Remains from Zhirendong, South China, and Modern Human Emergence in East Asia
    Human remains from Zhirendong, South China, and modern human emergence in East Asia Wu Liua,1, Chang-Zhu Jina, Ying-Qi Zhanga, Yan-Jun Caib, Song Xinga,c, Xiu-Jie Wua, Hai Chengd,e, R. Lawrence Edwardse, Wen-Shi Panf, Da-Gong Qinf, Zhi-Sheng Anb, Erik Trinkausg,1, and Xin-Zhi Wua aKey Laboratory of Evolutionary Systematics of Vertebrates, Institute of Vertebrate Paleontology and Paleoanthropology, Chinese Academy of Sciences, Beijing 100044, China; bState Key Laboratory of Loess and Quaternary Geology, Institute of Earth Environment, Chinese Academy of Sciences, Xi’an 710075, China; cGraduate School of the Chinese Academy of Sciences, Beijing 100049, China; dInstitute of Global Environmental Change, Xi’an Jiaotong University, Xi’an 710049, China; eDepartment of Geology and Geophysics, University of Minnesota, Minneapolis, MN 55455; fChongzuo Biodiversity Research Institute, Peking University, Chongzuo 532209, China; and gDepartment of Anthropology, Washington University, St. Louis, MO 63130 Contributed by Erik Trinkaus, September 24, 2010 (sent for review August 27, 2010) The 2007 discovery of fragmentary human remains (two molars supporting earlier dates for modern human presence in East and an anterior mandible) at Zhirendong (Zhiren Cave) in South Asia (cf. 12). China provides insight in the processes involved in the establish- This scenario implies a long term (>100,000 y) restriction of ment of modern humans in eastern Eurasia. The human remains early modern humans to portions of Africa with a brief ∼90 kya are securely dated by U-series on overlying flowstones and a rich expansion into extreme southwestern Asia, followed by a rela- associated faunal sample to the initial Late Pleistocene, >100 kya.
    [Show full text]