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Hybrid Vigor Between Native and Introduced Salamanders Raises New Challenges for Conservation
Hybrid vigor between native and introduced salamanders raises new challenges for conservation Benjamin M. Fitzpatrick*† and H. Bradley Shaffer‡ *Ecology and Evolutionary Biology, University of Tennessee, Knoxville, TN 37996; and ‡Evolution and Ecology, University of California, Davis, CA 95616 Edited by John C. Avise, University of California, Irvine, CA, and approved August 10, 2007 (received for review May 22, 2007) Hybridization between differentiated lineages can have many populations by alleviating inbreeding depression (13, 14) or different consequences depending on fitness variation among facilitating adaptive evolution in modified or degraded habitats hybrid offspring. When introduced organisms hybridize with na- (15–17). tives, the ensuing evolutionary dynamics may substantially com- The long-term consequences of hybridization are strongly plicate conservation decisions. Understanding the fitness conse- influenced by the genetic basis of hybrid fitness. In the case of quences of hybridization is an important first step in predicting its hybrid vigor, genetic models fall into two classes: heterozygote evolutionary outcome and conservation impact. Here, we mea- advantage and recombinant hybrid vigor (18–20). Heterozygote sured natural selection caused by differential viability of hybrid advantage (overdominance) refers to beneficial interactions larvae in wild populations where native California Tiger between heterospecific alleles of a single locus. Recombinant Salamanders (Ambystoma californiense) and introduced Barred hybrid vigor depends on multilocus genotypes and may be caused Tiger Salamanders (Ambystoma tigrinum mavortium) have been by epistasis (beneficial interactions between heterospecific al- hybridizing for 50–60 years. We found strong evidence of hybrid leles from different loci) or by complementary effects of inde- vigor; mixed-ancestry genotypes had higher survival rates than pendent advantageous alleles from each parental population (19, genotypes containing mostly native or mostly introduced alleles. -
Transformations of Lamarckism Vienna Series in Theoretical Biology Gerd B
Transformations of Lamarckism Vienna Series in Theoretical Biology Gerd B. M ü ller, G ü nter P. Wagner, and Werner Callebaut, editors The Evolution of Cognition , edited by Cecilia Heyes and Ludwig Huber, 2000 Origination of Organismal Form: Beyond the Gene in Development and Evolutionary Biology , edited by Gerd B. M ü ller and Stuart A. Newman, 2003 Environment, Development, and Evolution: Toward a Synthesis , edited by Brian K. Hall, Roy D. Pearson, and Gerd B. M ü ller, 2004 Evolution of Communication Systems: A Comparative Approach , edited by D. Kimbrough Oller and Ulrike Griebel, 2004 Modularity: Understanding the Development and Evolution of Natural Complex Systems , edited by Werner Callebaut and Diego Rasskin-Gutman, 2005 Compositional Evolution: The Impact of Sex, Symbiosis, and Modularity on the Gradualist Framework of Evolution , by Richard A. Watson, 2006 Biological Emergences: Evolution by Natural Experiment , by Robert G. B. Reid, 2007 Modeling Biology: Structure, Behaviors, Evolution , edited by Manfred D. Laubichler and Gerd B. M ü ller, 2007 Evolution of Communicative Flexibility: Complexity, Creativity, and Adaptability in Human and Animal Communication , edited by Kimbrough D. Oller and Ulrike Griebel, 2008 Functions in Biological and Artifi cial Worlds: Comparative Philosophical Perspectives , edited by Ulrich Krohs and Peter Kroes, 2009 Cognitive Biology: Evolutionary and Developmental Perspectives on Mind, Brain, and Behavior , edited by Luca Tommasi, Mary A. Peterson, and Lynn Nadel, 2009 Innovation in Cultural Systems: Contributions from Evolutionary Anthropology , edited by Michael J. O ’ Brien and Stephen J. Shennan, 2010 The Major Transitions in Evolution Revisited , edited by Brett Calcott and Kim Sterelny, 2011 Transformations of Lamarckism: From Subtle Fluids to Molecular Biology , edited by Snait B. -
Speciation in Heliconius Butterflies: Minimal Contact Followed 2 by Millions of Generations of Hybridisation 3 Simon H
bioRxiv preprint doi: https://doi.org/10.1101/015800; this version posted March 2, 2015. 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 4.0 International license. 1 1 Speciation in Heliconius Butterflies: Minimal Contact Followed 2 by Millions of Generations of Hybridisation 3 Simon H. Martin*1, Anders Eriksson*1,2, Krzysztof M. Kozak1, Andrea Manica1 and 4 Chris D. Jiggins1 5 1 Department of Zoology, University of Cambridge, Downing Street, Cambridge, CB2 6 3EJ, United Kingdom 7 2 Integrative Systems Biology Laboratory, King Abdullah University of Science 8 and Technology, Thuwal 23955-6900, Kingdom of Saudi Arabia 9 * These authors contributed equally 10 Corresponding Author: S.H. Martin, [email protected] 11 Running Head: Change in the rate of gene flow during butterfly speciation bioRxiv preprint doi: https://doi.org/10.1101/015800; this version posted March 2, 2015. 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 4.0 International license. 2 12 Abstract 13 Documenting the full extent of gene flow during speciation poses a challenge, as 14 species ranges change over time and current rates of hybridisation might not reflect 15 historical trends. Theoretical work has emphasized the potential for speciation in the 16 face of ongoing hybridisation, and the genetic mechanisms that might facilitate this 17 process. -
Hybrids and Hybrid Zones
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Digital.CSIC Hybrids and hybrid zones Arnold’s new book on hybridization1, recently reviewed by Ritchie in TREE 2, has brought attention to an old, controversial but revitalized topic in evolutionary biology. The two reviews2,3 we have read share a sceptical attitude towards studies of hybridization lying outside the hybrid zone theory. They consider Arnold’s book too ‘opinionated’2 and ‘an argument for a greater emphasis on the positive role of hybridization in evolution’ rather than a ‘comprehensive review’3. However, one of the merits of the book is that it devotes a great deal of effort towards reconciling divergent approaches to the topic. Arnold dedicates equal importance to animal and plant studies, as acknowledged by Ritchie2, and also puts much emphasis on the analysis of hybrid zones. In fact, when proposing a model for the birth of new evolutionary hybrid lineages he places his ‘new conceptual framework (the evolutionary novelty model)’ within the hybrid zone framework. Our criticism of this proposal is that it may be too rigid to fit scenarios departing from the specific model of hybrid speciation proposed by Grant4, that is, recombinational speciation. In our opinion, relying exclusively on the hybrid zone framework to assess the role of hybrids in evolution is misleading. Hybrid zones usually imply relatively recent events and species with strong reproductive barriers. The tension zone model assumes that hybrid zones are maintained by a balance between selection against hybrid individuals and dispersal of parental individuals into the hybrid zone5. -
An Anomalous Hybrid Zone in Drosophila
Evolution, 59(12), 2005, pp. 2602±2607 AN ANOMALOUS HYBRID ZONE IN DROSOPHILA ANA LLOPART,1,2 DANIEL LACHAISE,3,4 AND JERRY A. COYNE5,6 1Department of Biological Sciences, University of Iowa, 215 Biology Building (BB), Iowa City, Iowa 52242 2E-mail: [email protected] 3Centre National de la Recherche Scienti®que, Laboratoire Populations, GeÂneÂtique, et Evolution, 91198 Gif sur Yvette Cedex, France 4E-mail: [email protected] 5Department of Ecology and Evolution, University of Chicago, 1101 East 57 Street, Chicago, Illinois 60637 6E-mail: [email protected] Abstract. Despite the genetic tractability of many of Drosophila species, the genus has few examples of the ``classic'' type of hybrid zone, in which the ranges of two species overlap with a gradual transition from one species to another through an area where hybrids are produced. Here we describe a classic hybrid zone in Drosophila that involves two sister species, Drosophila yakuba and D. santomea, on the island of SaÄo TomeÂ. Our transect of this zone has yielded several surprising and anomalous ®ndings. First, we detected the presence of an additional hybrid zone largely outside the range of both parental species. This phenomenon is, to our knowledge, unique among animals. Second, the genetic analysis using diagnostic molecular markers of the ¯ies collected in this anomalous hybrid zone indicates that nearly all hybrid males are F1s that carry the D. santomea X chromosome. This F1 genotype is much more dif®cult to produce in the laboratory compared to the genotype from the reciprocal cross, showing that sexual isolation as seen in the laboratory is insuf®cient to explain the genotypes of hybrids found in the wild. -
Reproductive Isolation of Two Sympatric Louseworts, Pedicularis
Blackwell Publishing LtdOxford, UKBIJBiological Journal of the Linnean Society0024-4066© 2006 The Linnean Society of London? 2006 90? 3748 Original Article REPRODUCTIVE ISOLATION IN SYMPATRIC LOUSEWORTS C.-F. YANG ET AL . Biological Journal of the Linnean Society, 2007, 90, 37–48. With 4 figures Reproductive isolation of two sympatric louseworts, Pedicularis rhinanthoides and Pedicularis longiflora (Orobanchaceae): how does the same pollinator type avoid interspecific pollen transfer? CHUN-FENG YANG, ROBERT W. GITURU† and YOU-HAO GUO* College of Life Sciences, Wuhan University, Wuhan 430072, People’s Republic of China Received 11 April 2005; accepted for publication 1 March 2006 To study the isolation mechanism of two commonly intermingled louseworts, Pedicularis rhinanthoides and Pedic- ularis longiflora, pollination biology in three mixed populations with the two species was investigated during a 3- year project. The results indicated that higher flowering density could help to enhance pollinator activity, and thus increase reproductive output. Bumblebees are the exclusive pollinator for the two louseworts and are essential for their reproductive success. Reproductive isolation between the two species is achieved by a combination of pre- and postzygotic isolation mechanisms. Although both species are pollinated by bumblebees, the present study indicates they successfully avoid interspecific pollen transfer due to floral isolation. Mechanical isolation is achieved by the stigma in the two species picking up pollen from different parts of the pollinator’s body, whereas ethological isolation occurs due to flower constancy. Additionally, strong postzygotic isolation was demonstrated by non seed set after arti- ficial cross-pollination even with successful pollen tube growth. We describe the hitherto unreported role of variation in the tightness and direction of the twist of the corolla beak in maintaining mechanical isolation between Pedicu- laris species. -
Hybrid Fitness, Adaptation and Evolutionary Diversification: Lessons
Heredity (2012) 108, 159–166 & 2012 Macmillan Publishers Limited All rights reserved 0018-067X/12 www.nature.com/hdy REVIEW Hybrid fitness, adaptation and evolutionary diversification: lessons learned from Louisiana Irises ML Arnold, ES Ballerini and AN Brothers Estimates of hybrid fitness have been used as either a platform for testing the potential role of natural hybridization in the evolution of species and species complexes or, alternatively, as a rationale for dismissing hybridization events as being of any evolutionary significance. From the time of Darwin’s publication of The Origin, through the neo-Darwinian synthesis, to the present day, the observation of variability in hybrid fitness has remained a challenge for some models of speciation. Yet, Darwin and others have reported the elevated fitness of hybrid genotypes under certain environmental conditions. In modern scientific terminology, this observation reflects the fact that hybrid genotypes can demonstrate genotypeÂenvironment interactions. In the current review, we illustrate the development of one plant species complex, namely the Louisiana Irises, into a ‘model system’ for investigating hybrid fitness and the role of genetic exchange in adaptive evolution and diversification. In particular, we will argue that a multitude of approaches, involving both experimental and natural environments, and incorporating both manipulative analyses and surveys of natural populations, are necessary to adequately test for the evolutionary significance of introgressive hybridization. An appreciation of the variability of hybrid fitness leads to the conclusion that certain genetic signatures reflect adaptive evolution. Furthermore, tests of the frequency of allopatric versus sympatric/parapatric divergence (that is, divergence with ongoing gene flow) support hybrid genotypes as a mechanism of evolutionary diversification in numerous species complexes. -
Behavioural Mechanisms of Reproductive Isolation Between Two Hybridizing Dung Fly Species
Animal Behaviour 132 (2017) 155e166 Contents lists available at ScienceDirect Animal Behaviour journal homepage: www.elsevier.com/locate/anbehav Behavioural mechanisms of reproductive isolation between two hybridizing dung fly species * Athene Giesen , Wolf U. Blanckenhorn, Martin A. Schafer€ Institute of Evolutionary Biology and Environmental Studies, University of Zurich, Zurich, Switzerland article info Characterization of the phenotypic differentiation and genetic basis of traits that can contribute to Article history: reproductive isolation is an important avenue to understand the mechanisms of speciation. We quan- Received 29 November 2016 tified the degree of prezygotic isolation and geographical variation in mating behaviour among four Initial acceptance 26 January 2017 populations of Sepsis neocynipsea that occur in allopatry, parapatry or sympatry with four populations of Final acceptance 21 June 2017 its sister species Sepsis cynipsea. To obtain insights into the quantitative genetic basis and the role of selection against hybrid phenotypes we also investigated mating behaviour of F1 hybrid offspring and MS. number: 16-01039R corresponding backcrosses with the parental populations. Our study documents successful hybridization under laboratory conditions, with low copulation frequencies in heterospecific pairings but higher fre- Keywords: quencies in pairings of F1 hybrids signifying hybrid vigour. Analyses of F1 offspring and their parental biogeography backcrosses provided little evidence for sexual selection against hybrids. -
Can Secondary Contact Following Range Expansion Be Distinguished from Barriers to Gene flow?
Can secondary contact following range expansion be distinguished from barriers to gene flow? Johanna Bertl1,2, Harald Ringbauer3,4 and Michael G.B. Blum5 1 Department of Molecular Medicine, Aarhus University, Aarhus, Denmark 2 Vienna Graduate School of Population Genetics, Vetmeduni Vienna, Vienna, Austria 3 Department of Human Genetics, University of Chicago, Chicago, IL, USA 4 Institute of Science and Technology Austria, Klosterneuburg, Austria 5 Laboratoire TIMC-IMAG, UMR 5525, Université Grenoble Alpes, CNRS, Grenoble, France ABSTRACT Secondary contact is the reestablishment of gene flow between sister populations that have diverged. For instance, at the end of the Quaternary glaciations in Europe, secondary contact occurred during the northward expansion of the populations which had found refugia in the southern peninsulas. With the advent of multi-locus markers, secondary contact can be investigated using various molecular signatures including gradients of allele frequency, admixture clines, and local increase of genetic differentiation. We use coalescent simulations to investigate if molecular data provide enough information to distinguish between secondary contact following range expansion and an alternative evolutionary scenario consisting of a barrier to gene flow in an isolation-by-distance model. We find that an excess of linkage disequilibrium and of genetic diversity at the suture zone is a unique signature of secondary contact. We also find that the directionality index c, which was proposed to study range expansion, is informative to distinguish between the two hypotheses. However, although evidence for secondary contact is usually conveyed by statistics related to admixture coefficients, we find that they can be confounded by isolation-by-distance. We recommend to account for the spatial repartition of fl Submitted 29 November 2016 individuals when investigating secondary contact in order to better re ect the Accepted 1 July 2018 complex spatio-temporal evolution of populations and species. -
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 -
10 What Is a Species? Investigation • 3–4 C L a S S S E S S I O N S
10 What Is a Species? investigation • 3–4 c l a s s s e s s i o n s OVERVIEW MatERIals and adVanCE PREPaRatIOn In this activity students learn about the biological species For the teacher concept in defining species and how it provides information transparency of Scoring Guide: GROUP INTERACTION (GI) about where new species are in the process of separation transparency of Scoring Guide: UNDERSTANDING from closely related species. Students then investigate the CONCEPTS (UC) factors that lead to reproductive isolation of species. For each group of four students set of 14 Species Pairs Cards KEy COntEnt set of 8 Reproductive Barrier Cards 1. Species evolve over time. The millions of species that live chart paper* (optional) on the earth today are related by descent from common markers* (optional) ancestors. For each student 2. Taxa are classified in a hierarchy of groups and sub- Student Sheet 10.1, “Supporting a Scientific Argument” groups based on genealogical relationships. (optional) 3. The broad patterns of behavior exhibited by animals Scoring Guide: GROUP INTERACTION (GI) (optional) have evolved by natural selection as a result of reproduc- Scoring Guide: UNDERSTANDING CONCEPTS (UC) tive success. (optional) 4. Scientists have found that the original definition of spe- *Not supplied in kit cies as groups of organisms with similar morphology Decide in advance if you will hand out Student Sheet does not reflect underlying evolutionary processes. 10.1,“Supporting a Scientific Argument,” or have students 5. The biological species concept defines a species as a pop- record this information in their science notebooks. -
Coupling, Reinforcement, and Speciation Roger Butlin, Carole Smadja
Coupling, Reinforcement, and Speciation Roger Butlin, Carole Smadja To cite this version: Roger Butlin, Carole Smadja. Coupling, Reinforcement, and Speciation. American Naturalist, Uni- versity of Chicago Press, 2018, 191 (2), pp.155-172. 10.1086/695136. hal-01945350 HAL Id: hal-01945350 https://hal.archives-ouvertes.fr/hal-01945350 Submitted on 5 Dec 2018 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. Distributed under a Creative Commons Attribution| 4.0 International License vol. 191, no. 2 the american naturalist february 2018 Synthesis Coupling, Reinforcement, and Speciation Roger K. Butlin1,2,* and Carole M. Smadja1,3 1. Stellenbosch Institute for Advanced Study, Wallenberg Research Centre at Stellenbosch University, Stellenbosch 7600, South Africa; 2. Department of Animal and Plant Sciences, The University of Sheffield, Sheffield S10 2TN, United Kingdom; and Department of Marine Sciences, University of Gothenburg, Tjärnö SE-45296 Strömstad, Sweden; 3. Institut des Sciences de l’Evolution, Unité Mixte de Recherche 5554 (Centre National de la Recherche Scientifique–Institut de Recherche pour le Développement–École pratique des hautes études), Université de Montpellier, 34095 Montpellier, France Submitted March 15, 2017; Accepted August 28, 2017; Electronically published December 15, 2017 abstract: During the process of speciation, populations may di- Introduction verge for traits and at their underlying loci that contribute barriers Understanding how reproductive isolation evolves is key fl to gene ow.