Module 1: Anthropology, Science, and Storytelling
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Language Evolution to Revolution: from a Slowly Developing Finite Communication System with Many Words to Infinite Modern Language
bioRxiv preprint doi: https://doi.org/10.1101/166520; this version posted July 20, 2017. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Language evolution to revolution: from a slowly developing finite communication system with many words to infinite modern language Andrey Vyshedskiy1,2* 1Boston University, Boston, USA 2ImagiRation LLC, Boston, MA, USA Keywords: Language evolution, hominin evolution, human evolution, recursive language, flexible syntax, human language, syntactic language, modern language, Cognitive revolution, Great Leap Forward, Upper Paleolithic Revolution, Neanderthal language Abstract There is overwhelming archeological and genetic evidence that modern speech apparatus was acquired by hominins by 600,000 years ago. There is also widespread agreement that modern syntactic language arose with behavioral modernity around 100,000 years ago. We attempted to answer two crucial questions: (1) how different was the communication system of hominins before acquisition of modern language and (2) what triggered the acquisition of modern language 100,000 years ago. We conclude that the communication system of hominins prior to 100,000 years ago was finite and not- recursive. It may have had thousands of words but was lacking flexible syntax, spatial prepositions, verb tenses, and other features that enable modern human language to communicate an infinite number of ideas. We argue that a synergistic confluence of a genetic mutation that dramatically slowed down the prefrontal cortex (PFC) development in monozygotic twins and their spontaneous invention of spatial prepositions 100,000 years ago resulted in acquisition of PFC-driven constructive imagination (mental synthesis) and converted the finite communication system of their ancestors into infinite modern language. -
Chapter 4: Whai Can the Fossil Record Tell Lis About Human Origins?
anthropq what does it mean to be human? FOURTH EDITION Robert H. Lavenda St. Cloud State University Emily A. Schultz St. Cloud State University NewYork Oxford ^ot8OXFORD UNIVERSITY PRESS What can the fossil record tell us about human origi ns? Anthropology has made major contributions to our understanling of human biological and cultural evolution. This chapter tells the story of what we have learned from fossils, stone tools, and other cultural remains, from the appearance of our earliest known ancestors about 6 millioil years ago through the appearance of modern Homo sapiens about 200,000 years ago. CHAPTER OUTLINE What ls Macroevolution? The Culture of H. erectus What Do We Know about the What ls Hominin Evolution? H. erectusthe Hunter? Upper Paleolithic/Late Stone Who Were the First Hominins What Happened to H. erectus? Age (40,000?-1 2,000 Years Ago)? (6-3 mya)? How Did Homo sopiens Evolve? The Origin of Bipedalism What ls the Fossil Evidence for What Happened to the Changes in Hominin Dentition the Transition to Modern H. Neandertals? Who Were the Later sapiens? How Many Kinds of Upper Australopiths (3-1.5 mya)? Where Did Modern H. sapiens Paleolithic/Late Stone Age How Many Species of Come from? Cultures Were There? Australopith Were There? Who Were the Neandertals Where Did Modern H. sapiens How Can Anthropologists (1 30,000-35,000 Years Ago)? Migrate in Late Pleistocene Explain the Human Transition? What Do We Know about Times? What Do We Know about Early Middle Paleolithic/Middle Eastern Asia and Siberia Homo (2.4-1.5 mya)? -
Geographic Cline Analysis As a Tool for Studying Genome-Wide Variation: a Case Study of Pollinator-Mediated Divergence in a Monkeyflower
bioRxiv preprint doi: https://doi.org/10.1101/036954; this version posted January 15, 2016. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Geographic cline analysis as a tool for studying genome-wide variation: a case study of pollinator-mediated divergence in a monkeyflower Sean Stankowski1,2, James M. Sobel3 and Matthew A. Streisfeld1 1Institute of Ecology and Evolution, University of Oregon, Eugene, Oregon, United States of America 2Corresponding author E-mail: [email protected] 3Department of Biological Sciences, Binghamton University, Binghamton, New York, United States of America Keywords: ecotype formation, hybrid zone, Mimulus aurantiacus, pollinator isolation, reproductive isolation Running title: Genomics of pollinator-mediated divergence in a monkeyflower For consideration in the MEC special issue: The molecular basis of adaptation and ecological speciation - integrating genomic and molecular approaches; section: Ecological speciation genomics: advances and limitations 1 bioRxiv preprint doi: https://doi.org/10.1101/036954; this version posted January 15, 2016. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Abstract A major goal of speciation research is to reveal the genomic signatures that accompany the speciation process. Genome scans are routinely used to explore genome-wide variation and identify highly differentiated loci that may contribute to ecological divergence, but they do not incorporate spatial, phenotypic, or environmental data that might enhance outlier detection. -
Homo Erectus Infancy and Childhood the Turning Point in the Evolution of Behavioral Development in Hominids
10 Homo erectus Infancy and Childhood The Turning Point in the Evolution of Behavioral Development in Hominids Sue Taylor Parker In man, attachment is mediated by several different sorts of behaviour of which the most obvious are crying and calling, babbling and smiling, clinging, non-nutritional sucking, and locomotion as used in approach, following and seeking. —John Bowlby, Attachment The evolution of hominid behavioral ontogeny can be recon - structed using two lines of evidence: first, comparative neontological data on the behavior and development of living hominoid species (humans and the great apes), and second, comparative paleontolog- ical and archaeological evidence associated with fossil hominids. (Although behavior rarely fossilizes, it can leave significant traces.) 1 In this chapter I focus on paleontological and neontological evi - dence relevant to modeling the evolution of the following hominid adaptations: (1) bipedal locomotion and stance; (2) tool use and tool making; (3) subsistence patterns; (4) growth and development and other life history patterns; (5) childbirth; (6) childhood and child care; and (7) cognition and cognitive development. In each case I present a cladistic model for the origins of the characters in question. 2 Specifically, I review pertinent data on the following widely recog - nized hominid genera and species: Australopithecus species (A. afarensis , A. africanus , and A. robustus [Paranthropus robustus]) , early Homo species (Australopithecus gahri , Homo habilis , and Homo rudolfensis) , and Middle Pleistocene Homo species (Homo erectus , Homo ergaster , and others), which I am calling erectines . Copyrighted Material www.sarpress.org 279 S UE TAYLOR PARKER Table 10.1 Estimated Body Weights and Geological Ages of Fossil Hominids _______________________________________________________________________ Species Geologic Age Male Weight Female Weight (MYA) (kg) (kg) _______________________________________________________________________ A. -
UNIT 4 HISTORY of HUMAN EVOLUTION* History of Human Evolution
UNIT 4 HISTORY OF HUMAN EVOLUTION* History of Human Evolution Contents 4.0 Introduction 4.1 Trends in Human Evolution: Understanding Pre-modern Humans 4.2 Hominization Process 4.2.1 Bipedalism 4.2.2 Opposable Thumb and Manual Dexterity 4.3 Summary 4.4 References 4.5 Answers to Check Your Progress Learning Objectives: After reading this unit you will be able to: analyze the major trends in human evolution; review characteristics which distinguish human from their primate ancestors; learn anatomical and cultural changes associated with the process of hominization; and comprehend the significance of these changes during evolution of human. 4.0 INTRODUCTION Humans first evolved in East Africa about 2.5 million years ago from an earlier genus of apes called Australopithecus, which means ‘Southern Ape’. About 2 million years ago, some of these archaic men and women left their homeland to journey through and settle vast areas of North Africa, Europe and Asia. Since survival in the snowy forests of northern Europe required different traits than those needed to stay alive in Indonesia’s steaming jungles, human populations evolved in different directions. The result was several distinct species, to each of which scientists have assigned a pompous Latin name. Humans in Europe and western Asia evolved into Homo neanderthalensis (‘Man from the Neander Valley’), popularly referred to simply as ‘Neandethals’. Neanderthals, bulkier and more muscular than us Sapiens, were well adapted to the cold climate of Ice Age western Eurasia. The more eastern regions of Asia were populated by Homo erects, ‘Upright Man’, who survived there for close to 2 million years, making it the most durable species ever. -
Late Pleistocene Adult Mortality Patterns and Modern Human Establishment
Late Pleistocene adult mortality patterns and modern human establishment Erik Trinkaus1 Department of Anthropology, Washington University, St. Louis, MO 63130 Contributed by Erik Trinkaus, December 14, 2010 (sent for review November 29, 2010) The establishment of modern humans in the Late Pleistocene, after approximately 45 kyr B.P. that there are multiple indirect subsequent to their emergence in eastern Africa, is likely to have indications of such population increases, in at least some portions involved substantial population increases, during their initial of the Old World. Cultural traditions in both technology and or- dispersal across southern Asia and their subsequent expansions namentation become stable in some regions (11, 12), implying throughout Africa and into more northern Eurasia. An assessment more demographic stability (13). Evidence from stable isotopes of younger (20–40 y) versus older (>40 y) adult mortality distribu- and faunal remains suggests that populations were increasingly tions for late archaic humans (principally Neandertals) and two needing to exploit small package food resources requiring greater samples of early modern humans (Middle Paleolithic and earlier investment of acquisition effort (14–17). The demise of at least Upper Paleolithic) provides little difference across the samples. All one of the large Pleistocene carnivores, Ursus spelaeus, has been three Late Pleistocene samples have a dearth of older individuals attributed to increased competition for space from expanding compared with Holocene ethnographic/historical samples. They human populations, especially after approximately 50 kyr B.P. also lack older adults compared with Holocene paleodemographic (18, 19). And although body decoration appears sporadically profiles that have been critiqued for having too few older individ- earlier (20, 21), there was a marked increase in the social modi- uals for subsistence, social, and demographic viability. -
Recent Hybrids Recapitulate Ancient Hybrid Outcomes
Utah State University DigitalCommons@USU Ecology Center Publications Ecology Center 5-1-2020 Recent Hybrids Recapitulate Ancient Hybrid Outcomes Samridhi Chaturvedi Utah State University Lauren K. Lucas Utah State University C. Alex Buerkle University of Wyoming James A. Fordyce University of Tennessee, Knoxville Matthew L. Forister University of Nevada, Reno Chris C. Nice Texas State University See next page for additional authors Follow this and additional works at: https://digitalcommons.usu.edu/eco_pubs Part of the Ecology and Evolutionary Biology Commons Recommended Citation Chaturvedi, S., Lucas, L.K., Buerkle, C.A. et al. Recent hybrids recapitulate ancient hybrid outcomes. Nat Commun 11, 2179 (2020). https://doi.org/10.1038/s41467-020-15641-x This Article is brought to you for free and open access by the Ecology Center at DigitalCommons@USU. It has been accepted for inclusion in Ecology Center Publications by an authorized administrator of DigitalCommons@USU. For more information, please contact [email protected]. Authors Samridhi Chaturvedi, Lauren K. Lucas, C. Alex Buerkle, James A. Fordyce, Matthew L. Forister, Chris C. Nice, and Zachariah Gompert This article is available at DigitalCommons@USU: https://digitalcommons.usu.edu/eco_pubs/122 ARTICLE https://doi.org/10.1038/s41467-020-15641-x OPEN Recent hybrids recapitulate ancient hybrid outcomes Samridhi Chaturvedi1,2,3, Lauren K. Lucas1, C. Alex Buerkle 4, James A. Fordyce5, Matthew L. Forister6, ✉ Chris C. Nice7 & Zachariah Gompert1,2 Genomic outcomes of hybridization depend on selection and recombination in hybrids. Whether these processes have similar effects on hybrid genome composition in con- 1234567890():,; temporary hybrid zones versus ancient hybrid lineages is unknown. -
A CRITICAL EVALUATION of the LOWER-MIDDLE PALAEOLITHIC ARCHAEOLOGICAL RECORD of the CHALK UPLANDS of NORTHWEST EUROPE Lesley
A CRITICAL EVALUATION OF THE LOWER-MIDDLE PALAEOLITHIC ARCHAEOLOGICAL RECORD OF THE CHALK UPLANDS OF NORTHWEST EUROPE The Chilterns, Pegsdon, Bedfordshire (photograph L. Blundell) Lesley Blundell UCL Thesis submitted for the degree of PhD September 2019 2 I, Lesley Blundell, confirm that the work presented in this thesis is my own. Where information has been derived from other sources, I confirm that this has been indicated in the thesis. Signed: 3 4 Abstract Our understanding of early human behaviour has always been and continues to be predicated on an archaeological record unevenly distributed in space and time. More than 80% of British Lower-Middle Palaeolithic findspots were discovered during the late 19th/early 20th centuries, the majority from lowland fluvial contexts. Within the British planning process and some academic research, the resultant findspot distributions are taken at face value, with insufficient consideration of possible bias resulting from variables operating on their creation. This leads to areas of landscape outside the river valleys being considered to have only limited archaeological potential. This thesis was conceived as an attempt to analyse the findspot data of the Lower-Middle Palaeolithic record of the Chalk uplands of southeast Britain and northern France within a framework complex enough to allow bias in the formation of findspot distribution patterns and artefact preservation/discovery opportunities to be identified and scrutinised more closely. Taking a dynamic, landscape = record approach, this research explores the potential influence of geomorphology, 19th/early 20th century industrialisation and antiquarian collecting on the creation of the Lower- Middle Palaeolithic record through the opportunities created for artefact preservation and release. -
Natural Selection Maintains a Singlelocus Leaf Shape Cline In
Molecular Ecology (2013) 22, 552–564 doi: 10.1111/mec.12057 Natural selection maintains a single-locus leaf shape cline in Ivyleaf morning glory, Ipomoea hederacea BRANDON E. CAMPITELLI* and JOHN R. STINCHCOMBE*† *Department of Ecology and Evolutionary Biology, University of Toronto, 25 Willcocks Street, Toronto, ON Canada M5S 3B2, †Center for the Analysis of Genome Evolution and Function, University of Toronto, 25 Willcocks Street, Toronto, ON M5S 3B2, Canada Abstract Clines in phenotypic traits with an underlying genetic basis potentially implicate natu- ral selection. However, neutral evolutionary processes such as random colonization, spatially restricted gene flow, and genetic drift could also result in similar spatial pat- terns, especially for single-locus traits because of their susceptibility to stochastic events. One way to distinguish between adaptive and neutral mechanisms is to com- pare the focal trait to neutral genetic loci to determine whether neutral loci demon- strate clinal variation (consistent with a neutral cline), or not. Ivyleaf morning glory, Ipomoea hederacea, exhibits a latitudinal cline for a Mendelian leaf shape polymor- phism in eastern North America, such that lobed genotypes dominate northern popula- tions and heart-shaped genotypes are restricted to southern populations. Here, we evaluate potential evolutionary mechanisms for this cline by first determining the allele frequencies at the leaf shape locus for 77 populations distributed throughout I. hederacea’s range and then comparing the geographical pattern at this locus to neu- tral amplified fragment length polymorphism (AFLP) loci. We detected both significant clinal variation and high genetic differentiation at the leaf shape locus across all popu- lations. In contrast, 99% of the putatively neutral loci do not display clinal variation, and I. -
Spatial Mosaic Evolution of Snail Defensive Traits
University of New Orleans ScholarWorks@UNO Biological Sciences Faculty Publications Department of Biological Sciences 2007 Spatial Mosaic Evolution of Snail Defensive Traits Steve G. Johnson University of New Orleans, [email protected] Follow this and additional works at: https://scholarworks.uno.edu/biosciences_facpubs Recommended Citation Johnson, S.G., C. Darrin Hulsey, Francisco J. Garcia de Leon. 2007. Spatial mosaic evolution of snail defensive traits. BMC Evolutionary Biology 7:50 (open access in pubmed central) This Article is brought to you for free and open access by the Department of Biological Sciences at ScholarWorks@UNO. It has been accepted for inclusion in Biological Sciences Faculty Publications by an authorized administrator of ScholarWorks@UNO. For more information, please contact [email protected]. BMC Evolutionary Biology BioMed Central Research article Open Access Spatial mosaic evolution of snail defensive traits Steven G Johnson*1, C Darrin Hulsey2 and Francisco J García de León3 Address: 1Department of Biological Sciences, University of New Orleans, 2000 Lake Shore Drive, New Orleans, LA, 70148 USA, 2Department of Biology, Georgia Tech, 310 Ferst Drive, Atlanta, Georgia, 30332, USA and 3Centro de Investigaciones Biologicas del Noroeste, P.O. Box 128, La Paz, B.C.S. Mexico Email: Steven G Johnson* - [email protected]; C Darrin Hulsey - [email protected]; Francisco J García de León - [email protected] * Corresponding author Published: 30 March 2007 Received: 26 February 2007 Accepted: 30 March 2007 BMC Evolutionary Biology 2007, 7:50 doi:10.1186/1471-2148-7-50 This article is available from: http://www.biomedcentral.com/1471-2148/7/50 © 2007 Johnson et al; licensee BioMed Central Ltd. -
Genetic Exchange Across a Hybrid Zone Within the Iberian Endemic
Molecular Ecology (2005) 14, 245–254 doi: 10.1111/j.1365-294X.2004.02390.x GeneticBlackwell Publishing, Ltd. exchange across a hybrid zone within the Iberian endemic golden-striped salamander, Chioglossa lusitanica F. SEQUEIRA,*† J. ALEXANDRINO,*§ S. ROCHA,* J. W. ARNTZEN*‡ and N. FERRAND*† *CIBIO/UP-Centro de Investigação em Biodiversidade e Recursos Genéticos, Campus Agrário de Vairão, Rua Padre Armando Quintas, 4485–661 Vairão, Portugal, †Departamento de Zoologia e Antropologia, Faculdade de Ciências, Universidade do Porto, Praça Gomes Teixeira, 4099-002 Porto, Portugal, ‡National Museum of Natural History, PO Box 9517, 2300 RA Leiden, the Netherlands, §Museum of Vertebrate Zoology, University of California, Berkeley, 3101 Valley Life Science Building # 3160, Berkeley, CA 94720– 3160, USA Abstract The study of hybrid zones resulting from Pleistocene vicariance is central in examining the potential of genetically diverged evolutionary units either to introgress and merge or to proceed with further isolation. The hybrid zone between two mitochondrial lineages of Chioglossa lusitanica is located near the Mondego River in Central Portugal. We used mito- chondrial and nuclear diagnostic markers to conduct a formal statistical analysis of the Chioglossa hybrid zone in the context of tension zone theory. Key results are: (i) cline centres are not coincident for all markers, with average widths of ca. 2–15 km; (ii) heterozygote deficit was not observed across loci near the transect centre; (iii) associations of parental allele combinations (‘linkage disequilibrium’ R) were not detected either across loci or across the transect. These observations suggest that the Chioglossa hybrid zone is not a tension zone with strong selection against hybrids but instead one shaped mostly by neutral mixing. -
Microevolution: Species Concept Core Course: ZOOL3014 B.Sc. (Hons’): Vith Semester
Microevolution: Species concept Core course: ZOOL3014 B.Sc. (Hons’): VIth Semester Prof. Pranveer Singh Clines A cline is a geographic gradient in the frequency of a gene, or in the average value of a character Clines can arise for different reasons: • Natural selection favors a slightly different form along the gradient • It can also arise if two forms are adapted to different environments separated in space and migration (gene flow) takes place between them Term coined by Julian Huxley in 1838 Geographic variation normally exists in the form of a continuous cline A sudden change in gene or character frequency is called a stepped cline An important type of stepped cline is a hybrid zone, an area of contact between two different forms of a species at which hybridization takes place Drivers and evolution of clines Two populations with individuals moving between the populations to demonstrate gene flow Development of clines 1. Primary differentiation / Primary contact / Primary intergradation Primary differentiation is demonstrated using the peppered moth as an example, with a change in an environmental variable such as sooty coverage of trees imposing a selective pressure on a previously uniformly coloured moth population This causes the frequency of melanic morphs to increase the more soot there is on vegetation 2. Secondary contact / Secondary intergradation / Secondary introgression Secondary contact between two previously isolated populations Two previously isolated populations establish contact and therefore gene flow, creating an