Human Evolution

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Human Evolution Human Evolution "Most scientists believe that science generally approaches ever nearer to an objective description and understanding of its subject matter -- objective both in "Honey you may have come from monkeys, but I the sense that one scientist's description or conclusion sure didn't" -- Mrs. Guilleroy, elementary school can be achieved independently by others, and in the sense that his or her conclusions are not dictated by teacher, DeSoto, MO emotion, desire, or a priori expectations" -- Douglas Futuyma Phylogenetic relationships “Light will be thrown on the origin of man Order Primates Suborder Prosimii and his history.” Infraorder Lemuriformes (lemurs) Infraoder Lorisoformes (galagos, lorises) Suborder Tarsiiformes (tarsiers) -- Darwin, 1859 Suborder Anthropoidea Infraorder Platyrrhini (New World primates) Infraorder Catarrhini Superfamily Cercopithecoidea (Old World monkeys) Superfamily Hominoidea Family Hylobatidae (gibbons) Family Hominidae Subfamily Ponginae (orangutan) Subfamily Homininae (gorillas, chimps, Charles Darwin bonobos, humans) Human Origins & Evolution: Humans in same clade as African Great Apes Most parsimonious tree Molecular Evidence - mtDNA tree Humans, Chimps/Bonobos, and Gorillas are a H, C, G relationship monophyletic clade. A) Molecular & Morphological Bonobo Evidence G C B H Fig. 19.4 Human Origins & Evolution: Human Origins & Evolution: Key Points Human Origins & Evolution Morphological Evidence 1) Humans evolved from knuckle walker Fig 19.16 Behavior- Knuckle walking -Shared by G & C, but not in H 2) Humans and Chimps are closest living relatives Fossil- Dryopithicus (10mya fossil) A) Molecular & Recent Morphological Evidence -”woodland ape” “The Progress of Man” G C B H -shared characters with G, but not C & H •Bush, not a ladder Fossilized and extant wrist bones - •Multiple species coexisted •Exact relationships unclear -comparative study (G ancestral, C & H derived) Ardipithecus ramidus Gracile Australopithicines Human Origins & Evolution Ardipithecus ramidus Early hominid Approx. 4.4 mya East Africa Possibly bipedal? Forest dwelling Figure 19.15 Australopithecus afarensis Gracile Australopithicines Australopithecus afarensis Fig. 19.11 How do we know they were bipedal? Tanzania, Africa 1. Skeletal structure 3.0-3.9 mya 2. Fossilized footprints Australopithecus afarensis “Lucy” Under 5 ft tall Sexually dimorphic Prognathism Figure 19.15 Brain:400-500 cm3 Bipedal “Lucy” Bipedal Bipedalism Homo habilis Homo habilis Why did bipedalism evolve? 1. To see over savannah Moderate brain size grasses All African (?) Stone Tool use (Fig. 19.29) 2. To free hands to carry H. habilis Reduced Prognathism food 1.9-1.6 mya (Ancestors living in forest) Figure 19.15 Fig. 19.27 Homo erectus Homo erectus Homo erectus Homo erectus Widespread use of Fire! Expansion of brain size 1.2-0.4 mya H. erectus: 700 cm3 1st H. sapiens (Cro-magnon): 1,600 cm3 Modern: 1,200 cm3 Figure 19.15 The genus Homo: H. floresiensis Homo floresiensis Homo neanderthalensis H. Sapiens “The Hobbit” 0 H. neanderthalensis H. helmei 0.4 18,000 H. heidelbergensis years ago 0.8 H. cepranensis H. antecessor 1.2 H. floresiensis H. erectus 1.6 H. georgensis Millions of years ago H. ergaster Figure 19.15 2.0 Homo Neanderthalensis Homo Neanderthalensis Homo Neanderthalensis What happened to Neandertals? •Hybridization with H. sapiens? •Elimination by H. sapiens? H. Neanderthalensis H. Neanderthalensis H. Neanderthalensis 300 to 30 kya 300 to 30 kya 300 to 30 kya Tool use (Fig. 19.29) Language (Fig. 19.30) Large brains Figure 19.21 Homo Neanderthalensis Modern humans: Homo sapien Homo sapien: Brain Size Sequencing the Neanderthal Genome What is a human? Fig. 19.31 •Genetic differences between Opposable thumb H. sapiens and our close Bipedal relative Large brain •Possbile role of hybridization Tool making Language Creativity November 16, 2006!! Modern Humans Where did modern humans arise? African Replacement Supported by fossil How did intelligence and reason evolve? evidence (continuity of morphological •Tool use traits within regions) •Social interactions (e.g. parental care) •Possibly, selection for problem solving - Fig. 19.22 & 19.24 competition and cooperation for limited resources Multi-regional theory “Single African Origin” Most-recent common ancestor: •Lived in Africa •120 to 220 kya African replacement (“Out of Africa”) African replacement African replacement Human Evolution: Summary neandertals African replacement African replacement Predict: Genetic diversity should decrease when moving away from the Flores humans source. H. erectus, >1 mya H. sapiens, 250 yka.
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  • Development Team
    Paper No. : 14 Human Origin and Evolution Module : 09 Classification and Distribution of Living Primates Development Team Principal Investigator Prof. Anup Kumar Kapoor Department of Anthropology, University of Delhi Dr. Satwanti Kapoor (Retd Professor) Paper Coordinator Department of Anthropology, University of Delhi Mr. Vijit Deepani & Prof. A.K. Kapoor Content Writer Department of Anthropology, University of Delhi Prof. R.K. Pathak Content Reviewer Department of Anthropology, Panjab University, Chandigarh 1 Classification and Distribution of Living Primates Anthropology Description of Module Subject Name Anthropology Paper Name Human Origin and Evolution Module Name/Title Classification and Distribution of Living Primates Module Id 09 Contents: Primates: A brief Outline Classification of Living Primates Distribution of Living Primates Summary Learning Objectives: To understand the classification of living primates. To discern the distribution of living primates. 2 Classification and Distribution of Living Primates Anthropology Primates: A brief Outline Primates reside at the initial stage in the series of evolution of man and therefore constitute the first footstep of man’s origin. Primates are primarily mammals possessing several basic mammalian features such as presence of mammary glands, dense body hair; heterodonty, increased brain size, endothermy, a relatively long gestation period followed by live birth, considerable capacity for learning and behavioural flexibility. St. George J Mivart (1873) defined Primates (as an order)
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  • Fascinating Primates 3/4/13 8:09 AM Ancient Egyptians Used Traits of an Ibis Or a Hamadryas Used Traits Egyptians Ancient ) to Represent Their God Thoth
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  • Diagnosis and Differentiation of the Order Primates
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  • Amplification Dynamics of Platy-1 Retrotransposons in the Cebidae
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  • An Alu-Based Phylogeny of Lemurs (Infraorder: Lemuriformes)
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  • The Tempo of Trophic Evolution in Small-Bodied Primates 2 3 4 Running Title: Trophic Evolution in Small-Bodied Primates 5 6 7 Jeremiah E
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  • Monkeys and Prosimians: Social Learning D
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  • Subfossil Lemurs of Madagascar
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  • An Unusual Primate Locus That Attracted Two Independent Alu Insertions and Facilitates Their Transcription
    doi:10.1016/j.jmb.2005.03.058 J. Mol. Biol. (2005) 350, 200–214 An Unusual Primate Locus that Attracted Two Independent Alu Insertions and Facilitates their Transcription A. Ludwig, T. S. Rozhdestvensky, V. Yu. Kuryshev, J. Schmitz and J. Brosius* Institute of Experimental BC200 RNA, a neuronal, small non-messenger RNA that originated from a Pathology, ZMBE, University of monomeric Alu element is specific to anthropoid primates. Tarsiers lack an Mu¨nster, Von-Esmarch-Str. 56 insert at the orthologous genomic position, whereas strepsirrhines D-48149 Mu¨nster, Germany (Lemuriformes and Lorisiformes) acquired a dimeric Alu element, independently from anthropoids. In Galago moholi, the CpG dinucleotides are conspicuously conserved, while in Eulemur coronatus a large proportion is changed, indicating that the G. moholi Alu is under purifying selection and might be transcribed. Indeed, Northern blot analysis of total brain RNA from G. moholi with a specific probe revealed a prominent signal. In contrast, a corresponding signal was absent from brain RNA from E. coronatus. Isolation and sequence analysis of additional strepsirrhine loci confirmed the differential sequence conservation including CpG patterns of the orthologous dimeric Alu elements in Lorisiformes and Lemuriformes. Interestingly, all examined Alu elements from Lorisiformes were transcribed, while all from Lemuriformes were silent when transiently transfected into HeLa cells. Upstream sequences, especially those between the transcriptional start site and K22 upstream, were important for basal transcriptional activity. Thus, the BC200 RNA gene locus attracted two independent Alu insertions during its evolutionary history and provided upstream promoter elements required for their transcription. q 2005 Elsevier Ltd. All rights reserved.
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  • Macroevolutionary Dynamics and Historical Biogeography of Primate Diversification Inferred from a Species Supermatrix
    Macroevolutionary Dynamics and Historical Biogeography of Primate Diversification Inferred from a Species Supermatrix Mark S. Springer1*, Robert W. Meredith1,2, John Gatesy1, Christopher A. Emerling1, Jong Park1,3, Daniel L. Rabosky4,5, Tanja Stadler6, Cynthia Steiner7, Oliver A. Ryder7, Jan E. Janecˇka8, Colleen A. Fisher8, William J. Murphy8* 1 Department of Biology, University of California Riverside, Riverside, California, United States of America, 2 Department of Biology and Molecular Biology, Montclair State University, Montclair, New Jersey, United States of America, 3 Department of Biology, University of Washington, Seattle, Washington, United States of America, 4 Department of Integrative Biology, University of California, Berkeley, California, United States of America, 5 Department of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, Michigan, United States of America, 6 Institut fu¨r Integrative Biologie, Eidgeno¨ssiche Technische Hochschule Zurich, Zurich, Switzerland, 7 San Diego Zoo Institute for Conservation Research, San Diego Zoo Global, San Diego, California, United States of America, 8 Department of Veterinary Integrative Biosciences, Texas A&M University, College Station, Texas, United States of America Abstract Phylogenetic relationships, divergence times, and patterns of biogeographic descent among primate species are both complex and contentious. Here, we generate a robust molecular phylogeny for 70 primate genera and 367 primate species based on a concatenation of 69 nuclear gene segments and ten mitochondrial gene sequences, most of which were extracted from GenBank. Relaxed clock analyses of divergence times with 14 fossil-calibrated nodes suggest that living Primates last shared a common ancestor 71–63 Ma, and that divergences within both Strepsirrhini and Haplorhini are entirely post-Cretaceous.
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  • Lemurs of Madagascar and the Comoros the Lucn Red Data Book
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  • The Primate Order
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