What Is Natural Selection?
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And Ford, I; Ford, '953) on the Other Hand Have Put Forward a View Intermediate Between the Extreme Ones of Darwin on the One Hand and Goldschmidt on the Other
THE EVOLUTION OF MIMICRY IN THE BUTTERFLY PAPILIO DARDANUS C. A. CLARKE and P. M. SHEPPARD Departments of Medicine and Zoology, University of Liverpool Received23.V.59 1.INTRODUCTION WHENBatesputforward the mimicry hypothesis which bears his name, Darwin (1872), although accepting it, had some difficulty in explaining the evolution of the mimetic resemblance of several distinct species to one distasteful model by a series of small changes, a require- ment of his general theory of evolution. He said "it is necessary to suppose in some cases that ancient members belonging to several distinct groups, before they had diverged to their present extent, accidentally resembled a member of another and protected group in a sufficient degree to afford some slight protection; this having given the basis for the subsequent acquisition of the most perfect resemb- lance ". Punnett (1915) realised that the difficulty is even more acute when one is dealing with a polymorphic species whose forms mimic very distantly related models. Knowing that, in those butterflies which had been investigated genetically, the forms differed by single allelomorphs he concluded that the mimicry did not evolve gradually and did not confer any advantage or disadvantage to the individual. He argued that an allelomorph arises at a single step by mutation and that therefore the mimicry also arises by chance at a single step. Goldschmidt (x) although not denying that mimicry confers some advantage to its possessors also maintained that the resemblance arises fully perfected by a single mutation of a gene distinct from that producing the colour pattern in the model, but producing a similar effect in the mimic. -
Evolution Activity, Grade 11
Evolution Activity, Grade 11 Evolution Activities for Grade 11 Students at the Toronto Zoo 1 Evolution Activity, Grade 11 Table of Contents Pre-Zoo Activity 3-8 • Think, Pair, Share – Animals in Society and Role of Zoos 3-5 o Description 3 o Materials 3 o Four Corners Activity 6 o Background Information 7-8 Zoo Activity 9-19 • Teacher’s Notes 9-13 o General Information, Curriculum expectations, 9-10 materials, procedure o Evaluation Rubrics 11-12 o Glossary 13 • Student Assignment 14-19 o Part 1 – Mission Preparation at the Zoo 15-16 (Observation Sheets) o Part 2 – Scientific Notes 17 o Part 3 – Documentation: The Story 18 o Appendix – Animal signs 19 Evaluation 20 2 Evolution Activity, Grade 11 Suggested Pre-zoo activity Time needed : 35 minutes (or more) Type of activity : pair-share, small-group (approximately 2-3 students) Objective : encourage students to think about and evaluate the roles of animals in our society and the purposes of zoos along with their own attitudes or stands toward zoos Materials needed : a set of 8-16 statements and a mode of ranking (either above the line-below the line or diamond style ranking system) Special note : In order to manage time, teacher can chose to use any number of the statements as long as the 4 core statements listed bellow are included. Task : students work together to rank the statements about the treatment of animals. They should work together and try to negotiate a consensus, but if this is impossible they can either leave out the particular statement or write down a few lines in their notes as to why they would place them in a different category. -
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. -
Divergent Evolution in Antiherbivore Defences Within Species Complexes at a Single Amazonian Site
Journal of Ecology 2015, 103, 1107–1118 doi: 10.1111/1365-2745.12431 Divergent evolution in antiherbivore defences within species complexes at a single Amazonian site Marıa-Jose Endara1*, Alexander Weinhold1, James E. Cox2, Natasha L. Wiggins1, Phyllis D. Coley1,3 and Thomas A. Kursar1,3 1Department of Biology, The University of Utah, Salt Lake City, UT 84112-0840, USA; 2Health Sciences Center Core Research Facilities, School of Medicine, The University of Utah, Salt Lake City, UT 84112-0840, USA; and 3Smithsonian Tropical Research Institute, Balboa Box 0843-03092, Panama Summary 1. Classic theory in plant–insect interactions has linked herbivore pressure with diversification in plant species. We hypothesize that herbivores may exert divergent selection on defences, such that closely related plant species will be more different in defensive than in non-defensive traits. 2. We evaluated this hypothesis by investigating two clades of closely related plant species coexis- ting at a single site in the Peruvian Amazon: Inga capitata Desv. and Inga heterophylla Willd. spe- cies complexes. We compared how these lineages differ in the suite of chemical, biotic, phenological and developmental defences as compared to non-defensive traits that are related to habitat use and resource acquisition. We also collected insect herbivores feeding on the plants. 3. Our data show that sister lineages within both species complexes are more divergent in antiherbi- vore defences than in other non-defensive, functional traits. Moreover, the assemblages of herbivore communities are dissimilar between the populations of coexisting I. capitata lineages. 4. Synthesis. Our results are consistent with the idea that for the I. -
Patterns and Power of Phenotypic Selection in Nature
Articles Patterns and Power of Phenotypic Selection in Nature JOEL G. KINGSOLVER AND DAVID W. PFENNIG Phenotypic selection occurs when individuals with certain characteristics produce more surviving offspring than individuals with other characteristics. Although selection is regarded as the chief engine of evolutionary change, scientists have only recently begun to measure its action in the wild. These studies raise numerous questions: How strong is selection, and do different types of traits experience different patterns of selection? Is selection on traits that affect mating success as strong as selection on traits that affect survival? Does selection tend to favor larger body size, and, if so, what are its consequences? We explore these questions and discuss the pitfalls and future prospects of measuring selection in natural populations. Keywords: adaptive landscape, Cope’s rule, natural selection, rapid evolution, sexual selection henotypic selection occurs when individuals with selection on traits that affect survival stronger than on those Pdifferent characteristics (i.e., different phenotypes) that affect only mating success? In this article, we explore these differ in their survival, fecundity, or mating success. The idea and other questions about the patterns and power of phe- of phenotypic selection traces back to Darwin and Wallace notypic selection in nature. (1858), and selection is widely accepted as the primary cause of adaptive evolution within natural populations.Yet Darwin What is selection, and how does it work? never attempted to measure selection in nature, and in the Selection is the nonrandom differential survival or repro- century following the publication of On the Origin of Species duction of phenotypically different individuals. -
The Genetic Causes of Convergent Evolution
Nature Reviews Genetics | AOP, published online 9 October 2013; doi:10.1038/nrg3483 REVIEWS The genetic causes of convergent evolution David L. Stern Abstract | The evolution of phenotypic similarities between species, known as convergence, illustrates that populations can respond predictably to ecological challenges. Convergence often results from similar genetic changes, which can emerge in two ways: the evolution of similar or identical mutations in independent lineages, which is termed parallel evolution; and the evolution in independent lineages of alleles that are shared among populations, which I call collateral genetic evolution. Evidence for parallel and collateral evolution has been found in many taxa, and an emerging hypothesis is that they result from the fact that mutations in some genetic targets minimize pleiotropic effects while simultaneously maximizing adaptation. If this proves correct, then the molecular changes underlying adaptation might be more predictable than has been appreciated previously. (FIG. 1) Fitness Different species often evolve similar solutions to envi introgression . It is worth distinguishing between The potential evolutionary ronmental challenges. Insects, birds and bats evo these scenarios because each provides evidence for a dif success of a genotype, defined lved wings, and octopi, vertebrates and spiders ferent evolutionary path3. The first case, the independent as the reproductive success or evolved focusing eyes. Phenotypic convergence provides origin and spread of mutations, has been called parallel the proportion of genes that an individual leaves in the gene compelling evidence that ecological circumstances can genetic evolution. I suggest that the evolution of alleles 1,2 pool of the next generation in a select for similar evolutionary solutions . -
Arise by Chance As the Result of Mutation. They Therefore Suggest
THE EVOLUTION OF DOMINANCE UNDER DISRUPTIVE SELECTION C. A. CLARKE and P. Ni. SHEPPARD Department of Medicine and Department of Zoology, University of Liverpool Received6.iii.59 1.INTRODUCTION INa paper on the effects of disruptive selection, Mather (1955) pointed out that if there are two optimum values for a character and all others are less advantageous or disadvantageous there will be disruptive selection which can lead to the evolution of a polymorphism. Sheppard (1958) argued that where such selection is effective and the change from one optimum value to the other is switched by a single pair of allelomorphs there will be three genotypes but only two advantageous phenotypes. Consequently if dominance were absent initially it would be evolved as a result of the disruptive selection, the heterozygote and one of the homozygotes both coming to resemble one of the two optimum phenotypes (see Ford, 1955, on Tripharna comes). Thoday (1959) has shown by means of an artificial selection experiment that, even when a character is, at the beginning, controlled polygenically (sternopleural chaeta-number in Drosophila) and there is 50 per cent. gene exchange between the "high" and "low" selected sub-popu- lations, a polymorphism can evolve. The most fully understood examples of disruptive selection (other than sex) are provided by instances of Batesian Mimicry, where there are a number of distinct warningly coloured species, acting as models, which are mimicked by the polymorphic forms of a single more edible species. Fisher and Ford (see Ford, 1953) have argued that a suffi- ciently good resemblance between mimic and model is not likely to arise by chance as the result of mutation. -
Natural Selection One of the Most Important Contributions Made to The
Natural Selection One of the most important contributions made to the science of evolution by Charles Darwin is the concept of natural selection. The idea that members of a species compete with each other for resources and that individuals that are better adapted to their lifestyle have a better chance of surviving to reproduce revolutionized the field of evolution, though it was not accepted until several decades after Darwin first proposed it. Today, natural selection forms the foundation for our understanding of how species change over time. Natural selection may act to change a trait in many ways. When environmental pressures favor the average form of the trait, selection is said to be stabilizing. Directional selection occurs when selection pressures favor one extreme of the trait distribution. Selection is disruptive when the average form of the trait is selected against while either extreme is unaffected. In addition to natural selection, there are two other types of selection. Sexual selection, which Darwin believed was distinct from natural selection, involves the selection of traits based on their role in courtship and mating. Artificial selection is the selective breeding of species by humans to increase desirable traits, though the traits do not necessarily have to confer greater fitness. Summary of Types of Natural Selection Natural selection can take many forms. To make talking about this easier, we will consider the distribution of traits across a population in using a graph. To the right is a normal curve. For example, if we were talking about height as a trait, we would see that without any selection pressure on this trait, the heights of individuals in a population would vary, with most individuals being of an average height and fewer being extremely short or extremely tall. -
The Evolution of Mammalian Aging
Experimental Gerontology 37 &2002) 769±775 www.elsevier.com/locate/expgero The evolution of mammalian aging JoaÄo Pedro de MagalhaÄes*, Olivier Toussaint Department of Biology, Unit of Cellular Biochemistry and Biology, University of Namur FUNDP), Rue de Bruxelles 61, 5000 Namur, Belgium Received 18 December 2001; received in revised form 15 January 2002; accepted 18 January 2002 Abstract The incidence of aging is different between mammals and their closer ancestors &e.g. reptiles and amphibians). While all studied mammals express a well-de®ned aging phenotype, many amphibians and reptiles fail to show signs of aging. In addition, mammalian species show great similarities in their aging phenotype, suggesting that a common origin might be at work. The proposed hypothesis is that mammalian aging evolved together with the ancestry of modern mammals. In turn, this suggests that the fundamental cause of human aging is common to most, if not all, mammals and might be a unique phenom- enon. Experimental procedures capable of testing these theories and how to map the causes of mammalian and thus, human aging, are predicted. q 2002 Elsevier Science Inc. All rights reserved. Keywords: Aging; Senescence; Evolution; Mammals; Reptiles; Birds; Longevity 1. Introduction life span to Marion's tortoise capable of living over a century in captivity. Studies conducted in frogs failed Aging affects all studied mammalian species: from to indicate any increase in mortality both in the wild mice living no more than a mere half-a-dozen years to &Plytycz et al., 1995) and in captivity &Brocas and humans capable of living over 120years &Comfort, VerzaÁr, 1961). -
Consequences of the Domestication of Man's Best Friend, The
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology 289 Consequences of the Domestication of Man’s Best Friend, The Dog SUSANNE BJÖRNERFELDT ACTA UNIVERSITATIS UPSALIENSIS ISSN 1651-6214 UPPSALA ISBN 978-91-554-6854-5 2007 urn:nbn:se:uu:diva-7799 ! "# $ % &''( '!)'' * # * * +# #, "# - #, ./ * 0, &''(, 1 * # * $ 2 3 "# , 4 , &5!, 67 , , 809 !(5:!;:<<7:65<7:<, "# - # * # ;< ''' , " # # - # # = # , # - * # - * * # * * #, "# # * # # # # # 2 # # # # , " # - # - ) # # 94 # > # # , 8 1 # - # ** - # # # 2 * , 3 - * # - # # -# * , "# # * # # # * * * # # # , ? # * , * 1 * * - # *- * , @ - * # * - # -## * * , "# 1 # # # * * # * * , + 2 * # * - # - - # 2 , # > # -# * * - 1 * !" # $ # % # $ # & '( )*# # $+,-./0 # A 0 ./ * &''( 8009 ;6<;:6&;7 809 !(5:!;:<<7:65<7:< ) ))) :((!! B# )CC ,,C D E ) ))) :((!!F All knowledge, the totality of all questions and answers, is contained in the dog. FRANZ KAFKA, Investigations of the dog Cover photos by S Björnerfeldt List of Papers This thesis -
Biol2007 - Evolution of Quantitative Characters
1 BIOL2007 - EVOLUTION OF QUANTITATIVE CHARACTERS How do evolutionary biologists measure variation in a typical quantitative character? Let’s use beak size in birds as a typical example. Phenotypic variation (Vp) in a quantitative character Some of the variation in beak size is caused by environmental factors (VE). Some of the variation is caused by genetic factors (VG). If there was no variation in genotype between birds then individuals would differ in beak size only because of different rearing environments. Quantitative geneticists think in terms of how the value of a character in an individual compares to the mean value of the character in the population. The population mean is taken to be a neutral measure and then particular phenotypes are increases or decreases from that value. AT LEVEL OF INDIVIDUAL Phenotype = genotype + environment P = G + E AT LEVEL OF POPULATION Phenotypic variance = genotypic variance + environmental variance VP = VG + VE Genotypic variance is divided into additive, dominance and interaction components VG = VA + VD + V I VA = Additive variance – due to the additive effects of individual alleles (inherited) VD = Dominance variance - reflect the combinations of alleles at each locus (homo- versus (homozygotes versus hetero-zygotes) in any given generation but are not inherited by offspring. An intra-locus effect. VI = Interaction/epistatic variance - reflect epistatic interactions between alleles at different loci. Again not passed onto offspring; they depend on particular combinations of genes in a given generation and are not inherited by offspring. An inter-locus effect. ___________________________________________________________ The following section (italicised) provides the alebgra to backup my assertion that VD and VI are not heritable. -
FULLTEXT01.Pdf
Journal of Theoretical Biology 507 (2020) 110449 Contents lists available at ScienceDirect Journal of Theoretical Biology journal homepage: www.elsevier.com/locate/yjtbi The components of directional and disruptive selection in heterogeneous group-structured populations ⇑ Hisashi Ohtsuki a, , Claus Rueffler b, Joe Yuichiro Wakano c,d,e, Kalle Parvinen f,g, Laurent Lehmann h a Department of Evolutionary Studies of Biosystems, School of Advanced Sciences, SOKENDAI (The Graduate University for Advanced Studies), Shonan Village, Hayama, Kanagawa 240-0193, Japan b Animal Ecology, Department of Ecology and Genetics, University of Uppsala, Sweden c School of Interdisciplinary Mathematical Sciences, Meiji University, Tokyo 164-8525, Japan d Meiji Institute for Advanced Study of Mathematical Sciences, Tokyo 164-8525, Japan e Department of Mathematics, The University of British Columbia, 1984 Mathematics Road, Vancouver, B.C. V6T 1Z2, Canada f Department of Mathematics and Statistics, FI-20014 University of Turku, Finland g Evolution and Ecology Program, International Institute for Applied Systems Analysis (IIASA), A-2361 Laxenburg, Austria h Department of Ecology and Evolution, University of Lausanne, Switzerland article info abstract Article history: We derive how directional and disruptive selection operate on scalar traits in a heterogeneous group- Received 31 March 2020 structured population for a general class of models. In particular, we assume that each group in the Revised 5 August 2020 population can be in one of a finite number of states, where states can affect group size and/or other envi- Accepted 7 August 2020 ronmental variables, at a given time. Using up to second-order perturbation expansions of the invasion Available online 16 August 2020 fitness of a mutant allele, we derive expressions for the directional and disruptive selection coefficients, which are sufficient to classify the singular strategies of adaptive dynamics.