Evolution, Speciation, and Extinction College and AP Biology
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Unit-V Evolution of Horse
UNIT-V EVOLUTION OF HORSE Horses (Equus) are odd-toed hooped mammals belong- ing to the order Perissodactyla. Horse evolution is a straight line evolution and is a suitable example for orthogenesis. It started from Eocene period. The entire evolutionary sequence of horse history is recorded in North America. " Place of Origin The place of origin of horse is North America. From here, horses migrated to Europe and Asia. By the end of Pleis- tocene period, horses became extinct in the motherland (N. America). The horses now living in N. America are the de- scendants of migrants from other continents. Time of Origin The horse evolution started some 58 million years ago, m the beginning of Eocene period of Coenozoic era. The modem horse Equus originated in Pleistocene period about 2 million years ago. Evolutionary Trends The fossils of horses that lived in different periods, show that the body parts exhibited progressive changes towards a particular direction. These directional changes are called evo- lutionary trends. The evolutionary trends of horse evolution are summarized below: 1. Increase in size. 2. Increase in the length of limbs. 3. Increase in the length of the neck. 4. Increase in the length of preorbital region (face). 5. Increase in the length and size of III digit. 6. Increase in the size and complexity of brain. 7. Molarization of premolars. Olfactory bulb Hyracotherium Mesohippus Equus Fig.: Evolution of brain in horse. 8. Development of high crowns in premolars and molars. 9. Change of plantigrade gait to unguligrade gait. 10. Formation of diastema. 11. Disappearance of lateral digits. -
Evolution by Natural Selection, Formulated Independently by Charles Darwin and Alfred Russel Wallace
UNIT 4 EVOLUTIONARY PATT EVOLUTIONARY E RNS AND PROC E SS E Evolution by Natural S 22 Selection Natural selection In this chapter you will learn that explains how Evolution is one of the most populations become important ideas in modern biology well suited to their environments over time. The shape and by reviewing by asking by applying coloration of leafy sea The rise of What is the evidence for evolution? Evolution in action: dragons (a fish closely evolutionary thought two case studies related to seahorses) 22.1 22.4 are heritable traits that with regard to help them to hide from predators. The pattern of evolution: The process of species have changed evolution by natural and are related 22.2 selection 22.3 keeping in mind Common myths about natural selection and adaptation 22.5 his chapter is about one of the great ideas in science: the theory of evolution by natural selection, formulated independently by Charles Darwin and Alfred Russel Wallace. The theory explains how T populations—individuals of the same species that live in the same area at the same time—have come to be adapted to environments ranging from arctic tundra to tropical wet forest. It revealed one of the five key attributes of life: Populations of organisms evolve. In other words, the heritable characteris- This chapter is part of the tics of populations change over time (Chapter 1). Big Picture. See how on Evolution by natural selection is one of the best supported and most important theories in the history pages 516–517. of scientific research. -
Genomics and the Evolutionary History of Equids Pablo Librado, Ludovic Orlando
Genomics and the Evolutionary History of Equids Pablo Librado, Ludovic Orlando To cite this version: Pablo Librado, Ludovic Orlando. Genomics and the Evolutionary History of Equids. Annual Review of Animal Biosciences, Annual Reviews, 2021, 9 (1), 10.1146/annurev-animal-061220-023118. hal- 03030307 HAL Id: hal-03030307 https://hal.archives-ouvertes.fr/hal-03030307 Submitted on 30 Nov 2020 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Annu. Rev. Anim. Biosci. 2021. 9:X–X https://doi.org/10.1146/annurev-animal-061220-023118 Copyright © 2021 by Annual Reviews. All rights reserved Librado Orlando www.annualreviews.org Equid Genomics and Evolution Genomics and the Evolutionary History of Equids Pablo Librado and Ludovic Orlando Laboratoire d’Anthropobiologie Moléculaire et d’Imagerie de Synthèse, CNRS UMR 5288, Université Paul Sabatier, Toulouse 31000, France; email: [email protected] Keywords equid, horse, evolution, donkey, ancient DNA, population genomics Abstract The equid family contains only one single extant genus, Equus, including seven living species grouped into horses on the one hand and zebras and asses on the other. In contrast, the equine fossil record shows that an extraordinarily richer diversity existed in the past and provides multiple examples of a highly dynamic evolution punctuated by several waves of explosive radiations and extinctions, cross-continental migrations, and local adaptations. -
Skeleton of the Oligocene (30 Million-Year-Old) Horse, Mesohippus, Is a Featured Exhibit at the New North Dakota Cowboy Hall of Fame in Medora
Skeleton of the Oligocene (30 million-year-old) horse, Mesohippus, is a featured exhibit at the new North Dakota Cowboy Hall of Fame in Medora By John W. Hoganson Developers of the recently opened North Dakota Cowboy Hall of Fame contacted me about having a fossil exhibit in the new Hall in Medora. Of course, what would be more appropriate than an exhibit interpreting the evolution of the horse? Most people are under the false impression that horses did not inhabit North America until they were introduced by the Spaniards during the early days of conquest. But horses are indigenous to North America. Fossil remains of the earliest horse, referred to as Hyracotherium (or sometimes Eohippus), have been recovered from early Eocene (about 50 million years old) rocks in North America. In fact, they were some of the most abundant mammals that lived during that time. The fossil record of horses in North Dakota extends back to the Oligocene, about 30 million years ago, when the diminutive horse, Mesohippus roamed western North Dakota. Mesohippus was tiny, about the size of a sheep. The adults were only about 20 inches tall at the shoulder. They also had three toes on each foot compared to the modern horse Equus that has one. Mesohippus was also probably more of a browsing herbivore compared to the modern grazing horse. We have found many Mesohippus fossils in North Dakota but no complete skeletons. Consequently, the Mesohippus skeleton on exhibit at the Cowboy Hall of Fame is an exact cast replica. We have also found the remains of 50,000-year-old horses in North Dakota indicating that horses lived here during the last Ice Age. -
Microevolution and the Genetics of Populations Microevolution Refers to Varieties Within a Given Type
Chapter 8: Evolution Lesson 8.3: Microevolution and the Genetics of Populations Microevolution refers to varieties within a given type. Change happens within a group, but the descendant is clearly of the same type as the ancestor. This might better be called variation, or adaptation, but the changes are "horizontal" in effect, not "vertical." Such changes might be accomplished by "natural selection," in which a trait within the present variety is selected as the best for a given set of conditions, or accomplished by "artificial selection," such as when dog breeders produce a new breed of dog. Lesson Objectives ● Distinguish what is microevolution and how it affects changes in populations. ● Define gene pool, and explain how to calculate allele frequencies. ● State the Hardy-Weinberg theorem ● Identify the five forces of evolution. Vocabulary ● adaptive radiation ● gene pool ● migration ● allele frequency ● genetic drift ● mutation ● artificial selection ● Hardy-Weinberg theorem ● natural selection ● directional selection ● macroevolution ● population genetics ● disruptive selection ● microevolution ● stabilizing selection ● gene flow Introduction Darwin knew that heritable variations are needed for evolution to occur. However, he knew nothing about Mendel’s laws of genetics. Mendel’s laws were rediscovered in the early 1900s. Only then could scientists fully understand the process of evolution. Microevolution is how individual traits within a population change over time. In order for a population to change, some things must be assumed to be true. In other words, there must be some sort of process happening that causes microevolution. The five ways alleles within a population change over time are natural selection, migration (gene flow), mating, mutations, or genetic drift. -
Mammal Evolution
Mammal Evolution Geology 331 Paleontology Triassic synapsid reptiles: Therapsids or mammal-like reptiles. Note the sprawling posture. Mammal with Upright Posture From Synapsids to Mammals, a well documented transition series Carl Buell Prothero, 2007 Synapsid Teeth, less specialized Mammal Teeth, more specialized Prothero, 2007 Yanoconodon, Lower Cretaceous of China Yanoconodon, Lower Cretaceous of China, retains ear bones attached to the inside lower jaw Morganucodon Yanoconodon = articular of = quadrate of Human Ear Bones, or lower reptile upper reptile Auditory Ossicles jaw jaw Cochlea Mammals have a bony secondary palate Primary Palate Reptiles have a soft Secondary Palate secondary palate Reduction of digit bones from Hand and Foot of Permian Synapsid 2-3-4-5-3 in synapsid Seymouria ancestors to 2-3-3-3-3 in mammals Human Hand and Foot Class Mammalia - Late Triassic to Recent Superorder Tricodonta - Late Triassic to Late Cretaceous Superorder Multituberculata - Late Jurassic to Early Oligocene Superorder Monotremata - Early Cretaceous to Recent Superorder Metatheria (Marsupials) - Late Cretaceous to Recent Superorder Eutheria (Placentals) - Late Cretaceous to Recent Evolution of Mammalian Superorders Multituberculates Metatheria Eutheria (Marsupials) (Placentals) Tricodonts Monotremes . Live Birth Extinct: . .. Mammary Glands? Mammals in the Age of Dinosaurs – a nocturnal life style Hadrocodium, a lower Jurassic mammal with a “large” brain (6 mm brain case in an 8 mm skull) Were larger brains adaptive for a greater sense of smell? Big Brains and Early Mammals July 14, 2011 The Academic Minute http://www.insidehighered.com/audio/academic_pulse/big_brains_and_early_mammals Lower Cretaceous mammal from China Jawbones of a Cretaceous marsupial from Mongolia Mammal fossil from the Cretaceous of Mongolia Reconstructed Cretaceous Mammal Early Cretaceous mammal ate small dinosaurs Repenomamus robustus fed on psittacosaurs. -
Progress and Competition in Macroevolution
Biol . Rev . (1987). 62. pp. 305-338 Printed in Great Britain PROGRESS AND COMPETITION IN MACROEVOLUTION BY MICHAEL J . BENTON Department of Geology. The Queen’s University of Belfast. Belfast. BT7 INN. Northern Ireland (Received I 3 August 1985. accepted 23 February 1987) CONTENTS I . Introduction ........ I1. Improvements in competitive ability through time ........ (I) Evolutionary progress ............ (2) Increase in morphological complexity ......... (3) The expansion of life ............. (4) Evolutionary trends ............. (5) Increased effectiveness of adaptation .......... I11 . Competition in microevolution ........... (I) Competition and natural selection .......... (2) The evolutionary effects of interspecific competition ....... (3) The effects of interspecific competition on community structure .... IV . Competition in macroevolution ........... (I) Extinction and competition ........... (2) The Red Queen .............. (3) The community paradigm ............ (4) Evolutionary rates and competitive ability ......... V . Competition and major ecological replacements ........ (I) Key adaptations and replacements ........... (2) Patterns of ecological replacement ........... (3) The evidence for double-wedge patterns (differential survival) in the fossil record . (4) The evidence that differential survival was caused by competition .... (5) Alternatives to competition ........... VI . The problems of invoking large-scale competition ........ VII . Summary ................ VIII . Acknowledgements .............. IX. References -
Multiple Origins of Life (Extinction/Bioclade/Precambrian/Evolution/Stochastic Processes) DAVID M
Proc. Natt Acad. Sci. USA Vol. 80; pp. 2981-2984, May 1983 Evolution Multiple origins of life (extinction/bioclade/Precambrian/evolution/stochastic processes) DAVID M. RAUP* AND JAMES W. VALENTINEt *Department of the Geophysical Sciences, University of Chicago, Chicago, Illinois 60637; and tDepartment of Geological Sciences, University of California, Santa Barbara, California 93106 Contributed by David M. Raup, February 22, 1983 ABSTRACT There is some indication that life may have orig- ing a full assortment of prebiotically synthesized organic build- inated readily under primitive earth conditions. If there were ing blocks for life and conditions appropriate for life origins, it multiple origins of life, the result could have been a polyphyletic is possible that rates of bioclade origins might compare well biota today. Using simple stochastic models for diversification and enough with rates of diversification. Indeed, there has been extinction,-we conclude: (i) the probability of survival of life is low speculation that life may have been polyphyletic (1, 4). How- unless there are multiple origins, and (ii) given survival of life and ever, there is strong evidence that all living forms are de- given as many as 10 independent origins of life, the odds are that scended from a single ancestor. Biochemical and organizational all but one would have gone extinct, yielding the monophyletic biota similarities and the "universality" of the genetic code indicate we have now. The fact of the survival of our particular form of this. Therefore, the question for this paper is: If there were life does not imply that it was unique or superior. multiple bioclades early in life history, what is the probability that only one would have survived? In other words, if life The formation of life de novo is generally viewed as unlikely or orig- impossible under present earth conditions. -
Bruce J. Macfadden*
MacFadden, B.J., 2006, Early Pliocene (latest Hemphillian) horses from the Yepómera Local 33 Fauna, Chihuahua, Mexico, in Carranza-Castañeda, Óscar, and Lindsay, E.H., eds., Advances in late Tertiary vertebrate paleontology in Mexico and the Great American Biotic Interchange: Universidad Nacional Autónoma de México, Instituto de Geología and Centro de Geociencias, Publicación Especial 4, p. 33–43. EARLY PLIOCENE (LATEST HEMPHILLIAN) HORSES FROM THE YEPÓMERA LOCAL FAUNA, CHIHUAHUA, MEXICO Bruce J. MacFadden* ABSTRACT The latest Hemphillian (Hh4) is characterized by a distinctive equid assemblage, four spe- cies of which are widespread in North America. One of the largest collections of Hh4 equids is from Yepómera, located in Chihuahua, Mexico. Although Yepómera is actually a series of sub-localities, the equids are morphologically similar from each of these and therefore can be considered as a local faunal assemblage of four sympatric species. The distinctive dental patterns, size of the cheek teeth, and (in most cases) metapodial dimensions, make these horses readily distinguishable in the field. Yepómera equids include the monodactyl Astrohippus stockii and Dinohippus mexicanus, and tridactyl Neohipparion eurystyle and Nannippus aztecus. Yepómera is the type locality for the species A. stockii and D. mexica- nus, both described by Lance in 1950. Neohipparion eurystyle and the genus Neohipparion and A. stockii and the genus Astrohippus become extinct at the end of Hh4. Nannippus aztecus is a sister taxon of later Nannippus and D. mexicanus is the sister taxon of Equus, the equid genera that survived in North America during the Plio-Pleistocene. With hypsodonty indices between 2.6 and 3.7, all of the Yepómera horse species have high-crowned teeth, traditionally interpreted as a grazing adaptation. -
Biology 242 – Genomes & Evolution
Fall 2017 Biology 242 – Genomes & Evolution Instructor: Dr. Terry Bird Office: Shiley Center for Science and Technology 432 Laboratory: Shiley Center for Science and Technology 474 Phone #: (619) 260-4671 email: [email protected] Office hours: Mon, Tues & Wed 1:30-2:30pm, Thurs 12:30-2:30pm or by appointment Text: Campbell Biology (11th Edition) (Mastering Biology) Inquiry in Action: Interpreting Scientific Papers, Buskirk & Gillen A Student Handbook for Writing Biology, 4th ed., Karin Knisely Course description This one-semester course for biology majors provides an introduction to the mechanisms and results of information flow through organisms and their lineages. Lecture topics will include the nature, expression, and change of hereditary information in DNA, the mechanisms of evolution, and the origins and relationships of major groups of organisms. The laboratory (Bio 242L) must be taken concurrently and will include inquiry into the genetic basis of evolutionary change, and testing of hypotheses of adaptation. Bio 242 and Bio 242L constitute half of the year of introductory biology. Bio 240 and 240L, Bioenergetics and Systems, should be taken the semester before or after Bio 242. This introductory series meets the general biology requirements of the biology major and health science professional programs, as well as the Core requirement for Scientific and Technological Inquiry. Students in majors other than the sciences should consider taking designated biology courses below the 200-level to fulfill this Core requirement. Course Learning Outcomes At the end of the semester a student who takes both Bio 242 lecture and lab should be able to: 1. Design and conduct an experimental and/or observational investigation to generate scientific knowledge. -
Adaptation, Natural Selection and Evolution Learning Intentions • Give the Meaning of the Term Mutation
Adaptation, natural selection and evolution Learning Intentions • Give the meaning of the term mutation. • State that mutations may be neutral, confer an advantage or a disadvantage. • State that mutations are spontaneous and are the only source of new alleles. • Give two environmental factors which can increase the rate of mutation. • Give the meaning of the term adaptation. • Give examples of adaptations which allow a species to survive. • State that adaptation may be structural, physiological or behavioural. • Describe examples of behaviours which allow a species to survive. • State that variation within a population makes it possible for a population to evolve over time in response to changing conditions. • Describe natural selection/survival of the fittest. • Describe the process of speciation. Mutation • A mutation is a random change to the genetic material of an organism • Mutations are rare, random and spontaneous • Mutations can alter the phenotype or functioning of the organism. • Mutations which occur in sex cells are inherited by offspring, they are the only source of new alleles, and can alter the phenotype or functioning of the organism. Types of Mutation • Mutations can be neutral, an advantage or a disadvantage • Neutral – these have no effect on the organism • Confer an advantage – for example the peppered moth mutation which made moths dark in colour – this allowed them to be camouflaged in industrial areas with soot covering trees • Confer a disadvantage – for example a gene mutation in chromosome 7 in humans leads to cystic fibrosis Moths…how many can you see? Mutagenic Agents • The rate of mutations can be artificially increased by environmental factors such as: – Radiation such as X-rays, UV light, gamma rays – Chemicals like colchicine, mustard gas and benzene. -
The Cost of Evolution and the Imprecision of Adaptation (Haldane's Dilemma/Multi-Level Feedback/Human Evolution/Maximization) P
Proc. Natl. Acad. Sci. USA Vol. 74, No. 4, pp. 1647-1651, April 1977 Evolution The cost of evolution and the imprecision of adaptation (Haldane's dilemma/multi-level feedback/human evolution/maximization) P. J. DARLINGTON, JR. Museum of Comparative Zoology, Harvard University, Cambridge, Massachusetts 02138 Contributed by P. J. Darlington, Jr., January 21, 1977 ABSTRACT Comparisons of six hypothetical cases suggest Case B. Now suppose that the two survivors escape other that Haldane overestimated the cost ofnatural selection by al- hazards and produce ten offspring of which two (6 9) are lele substitution. The cost is reduced if recessive alleles are ad- homozygous for another recessive allele which allows them to vantageous, if substitutions are large and few, if selection is strong and substitutions are rapid, if substitutions are serial, and survive (say) a protein shortage which results in the deaths (or if substitutions in small demes are followed by deme-group failure to reproduce) of the other eight individuals. Then an- substitutions. But costs are still so heavy that the adaptations other complete allele substitution will have been made in one of complex organisms in complex and changing environments generation at a cost of are never completed. The rule probably is that most species most of the time are not fully adapted to their environments, but are No(10) - N1(2) = 8 just a little better than their competitors for the time being. individuals, and again no additional selective substitutions can During the "evolution" of a man-made machine, the maker be made and paid for at the same time.