Eventual-Question-33.Pdf

Total Page:16

File Type:pdf, Size:1020Kb

Eventual-Question-33.Pdf Sexual Selection, Species Recognition, and Speciation Reinforcement is the process by which two partially reproductively isolated species come into secondary contact with one another, and further reproductive isolating mechanisms are evolved to reduce or prevent hybridization between the two. Presumably, reinforcement evolves from the selection pressures to reduce hybridization. By definition, reinforcement cannot initiate the process of speciation to generate reproductive isolation, but it must act through selection on the same types of processes as at the initial stages of speciation. In this question, we would like for you to develop a narrative about the process of reinforcement and the issues raised by it along the following lines. First, briefly review the concept of reinforcement and the empirical evidence for the operation of the process. The classic model typically considers a system consisting of two parts: mate preference and a mating trait. The genetic architecture of these two components can shape the evolution of reinforcement and nonrandom mating in general. Expound on the genetic conditions for these two components can hasten or retard their evolution? Then break out of the classic model and evaluate various types of premating and postmating isolating mechanisms as effective evolutionary pathways to reducing the level of hybridization. In particular, many people focus on the further evolution of genetic incompatibilities as the outcome of reinforcement. However, pre- mating barriers to gene flow would seem to also work as well. In particular, focus on the relative advantages and disadvantages of each as the outcome of reinforcement, and highlight some real world examples of each type of isolating mechanism you discuss. Finally, consider the consequences of each of these types of mating barriers that may evolve via reinforcement to the intraspecific mating advantages of a species. Namely, how might the evolution of isolating mechanisms via reinforcement influence mating dynamics with conspecific partners – both for males and females. .
Recommended publications
  • 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 The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity.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.
    [Show full text]
  • Biol B242 - Coevolution
    BIOL B242 - COEVOLUTION http://www.ucl.ac.uk/~ucbhdjm/courses/b242/Coevol/Coevol.html BIOL B242 - COEVOLUTION So far ... In this course we have mainly discussed evolution within species, and evolution leading to speciation. Evolution by natural selection is caused by the interaction of populations/species with their environments. Today ... However, the environment of a species is always partly biotic. This brings up the possiblity that the "environment" itself may be evolving. Two or more species may in fact coevolve. And coevolution gives rise to some of the most interesting phenomena in nature. What is coevolution? At its most basic, coevolution is defined as evolution in two or more evolutionary entities brought about by reciprocal selective effects between the entities. The term was invented by Paul Ehrlich and Peter Raven in 1964 in a famous article: "Butterflies and plants: a study in coevolution", in which they showed how genera and families of butterflies depended for food on particular phylogenetic groupings of plants. We have already discussed some coevolutionary phenomena: For example, sex and recombination may have evolved because of a coevolutionary arms race between organisms and their parasites; the rate of evolution, and the likelihood of producing resistance to infection (in the hosts) and virulence (in the parasites) is enhanced by sex. We have also discussed sexual selection as a coevolutionary phenomenon between female choice and male secondary sexual traits. In this case, the coevolution is within a single species, but it is a kind of coevolution nonetheless. One of our problem sets involved frequency dependent selection between two types of players in an evolutionary "game".
    [Show full text]
  • Mating Preferences Might Evolve by Natural Selection. If Mating Mate
    A GENERAL MODEL OF SEXUAL AND NATURAL SELECTION P. O'DONALD Department of Zoology, University College of North Wales, bangor Received28.xii.66 1.INTRODUCTION FISHERin The Genetical Theory of JVatural Selection (1930) described how mating preferences might evolve by natural selection. If mating behaviour varies among different genotypes, some individuals may have an hereditary disposition to mate with others having particular characteristics. Usually of course it is the females who choose the males and their choice is determined by the likelihood that the males' display will release their mating responses. If some females prefer to mate with those males that have characteristics advantageous in natural selection, then the genotypes that determine such matings will also be selected: the offspring will carry both the advantageous geno- types and the genotypes of the mating preference. Once the mating preference is established, it will itself add to the selective advantage of the preferred genotypes: a "runaway process" as Fisher called it develops. In a paper in Heredity (1963) I described a mathematical model of this type of selection. In the simplest case two loci must be involved: one locus determines the preferred character and the other the mating preference. If there are only two alleles segregating at each locus, ten different genotypes can occur if the loci are linked and nine if they are not. If they are sex-linked, there are i possible genotypes. I derived finite difference equations giving the frequencies of the genotypes in terms of parameters describing the degree of dominance of the preferred genotypes and the recombination fractions of the loci.
    [Show full text]
  • Mate Choice | Principles of Biology from Nature Education
    contents Principles of Biology 171 Mate Choice Reproduction underlies many animal behaviors. The greater sage grouse (Centrocercus urophasianus). Female sage grouse evaluate males as sexual partners on the basis of the feather ornaments and the males' elaborate displays. Stephen J. Krasemann/Science Source. Topics Covered in this Module Mating as a Risky Behavior Major Objectives of this Module Describe factors associated with specific patterns of mating and life history strategies of specific mating patterns. Describe how genetics contributes to behavioral phenotypes such as mating. Describe the selection factors influencing behaviors like mate choice. page 882 of 989 3 pages left in this module contents Principles of Biology 171 Mate Choice Mating as a Risky Behavior Different species have different mating patterns. Different species have evolved a range of mating behaviors that vary in the number of individuals involved and the length of time over which their relationships last. The most open type of relationship is promiscuity, in which all members of a community can mate with each other. Within a promiscuous species, an animal of either gender may mate with any other male or female. No permanent relationships develop between mates, and offspring cannot be certain of the identity of their fathers. Promiscuous behavior is common in bonobos (Pan paniscus), as well as their close relatives, the chimpanzee (P. troglodytes). Bonobos also engage in sexual activity for activities other than reproduction: to greet other members of the community, to release social tensions, and to resolve conflicts. Test Yourself How might promiscuous behavior provide an evolutionary advantage for males? Submit Some animals demonstrate polygamous relationships, in which a single individual of one gender mates with multiple individuals of the opposite gender.
    [Show full text]
  • 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.
    [Show full text]
  • 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
    [Show full text]
  • 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.
    [Show full text]
  • Human Sexual Selection
    Available online at www.sciencedirect.com ScienceDirect Human sexual selection David Puts Sexual selection favors traits that aid in competition over Here, I review evidence, focusing on recent findings, mates. Widespread monogamous mating, biparental care, regarding the strength and forms of sexual selection moderate body size sexual dimorphism, and low canine tooth operating over human evolution and consider how sexual dimorphism suggest modest sexual selection operating over selection has shaped human psychology, including psy- human evolution, but other evidence indicates that sexual chological sex differences. selection has actually been comparatively strong. Ancestral men probably competed for mates mainly by excluding The strength of human sexual selection competitors by force or threat, and women probably competed Some evidence suggests that sexual selection has been primarily by attracting mates. These and other forms of sexual relatively weak in humans. Although sexual dimorphisms selection shaped human anatomy and psychology, including in anatomy and behavior may arise from other selective some psychological sex differences. forces, the presence of sexually dimorphic ornamentation, Address weaponry, courtship displays, or intrasexual competition Department of Anthropology and Center for Brain, Behavior and indicates a history of sexual selection [3]. However, men’s Cognition, Pennsylvania State University, University Park, PA 16802, 15–20% greater body mass than women’s is comparable to USA primate species with a modest degree of mating competi- tion among males, and humans lack the canine tooth Corresponding author: Puts, David ([email protected]) dimorphism characteristic of many primates with intense male competition for mates [4]. Moreover, humans exhibit Current Opinion in Psychology 2015, 7:28–32 biparental care and social monogamy, which tend to occur This review comes from a themed issue on Evolutionary psychology in species with low levels of male mating competition [5].
    [Show full text]
  • Plant Speciation
    PLANT SPECIATION Niarsi Merry Hemelda, M.Si. MK Keanekaragaman Tumbuhan Departemen Biologi FMIPA -UI OUTLINE: Evolution Modes of plant speciation Features of plant evolution Speciation EVOLUTION SPECIES The cumulative The basic biological change in the heritable unit around which characteristics of a classifications are population over time. based. Speciation: an evolutionary process by which a new species comes into being. Evolution Microevolution Macroevolution • Microevolution is a change in generally refers to evolution gene frequency in a population in above the species level. short period of time. • Processes that can directly affect gene frequencies in a population: (mutation, migration, genetic drift, non random mating, natural selection) Patterns of evolution: A. Divergent Evolution: the two species gradually become increasingly different. B. Convergent Evolution: species of different ancestry begin to share analogous traits because of a shared environment or other selection pressure C. Parallel Evolution: two species evolve independently of each other, maintaining the same level of similarity. Parallel evolution usually occurs between unrelated species that do not occupy the same or similar niches in a given habitat. How a new species originate: • Species are created by a series of evolutionary processes. • Classically, speciation has been viewed as a three stage process: oIsolation of populations. oDivergence in traits of separated populations (e.g. mating system or habitat use). oReproductive isolation of populations that maintains
    [Show full text]
  • Factors Influencing the Diversification of Mating Behavior of Animals
    International Journal of Zoology and Animal Biology ISSN: 2639-216X Factors Influencing the Diversification of Mating Behavior of Animals Afzal S1,2*, Shah SS1,2, Afzal T1, Javed RZ1, Batool F1, Salamat S1 and Review Article Raza A1 Volume 2 Issue 2 1Department of zoology, university of Narowal, Pakistan Received Date: January 28, 2019 Published Date: April 24, 2019 2Department of zoology, university of Punjab, Pakistan DOI: 10.23880/izab-16000145 *Corresponding author: Sabila Afzal, Department of zoology, University of Punjab, Pakistan, Email: [email protected] Abstract “Mating system” of a population refers to the general behavioral strategy employed in obtaining mates. In most of them one sex is more philopatric than the other. Reproductive enhancement through increased access to mates or resources and the avoidance of inbreeding are important in promoting sex differences in dispersal. In birds it is usually females which disperse more than males; in mammals it is usually males which disperse more than females. It is argued that the direction of the sex bias is a consequence of the type of mating system. Philopatry will favor the evolution of cooperative traits between members of the sedentary sex. It includes monogamy, Polygyny, polyandry and promiscuity. As an evolutionary strategy, mating systems have some “flexibility”. The existence of extra-pair copulation shows that mating systems identified on the basis of behavioral observations may not accord with actual breeding systems as determined by genetic analysis. Mating systems influence the effectiveness of the contraceptive control of pest animals. This method of control is most effective in monogamous and polygamous species.
    [Show full text]
  • Sexual Selection and Mate Choice
    Review TRENDS in Ecology and Evolution Vol.21 No.6 June 2006 Sexual selection and mate choice Malte Andersson1 and Leigh W. Simmons2 1Department of Zoology, University of Gothenburg, SE 405 30 Gothenburg, Sweden 2Centre for Evolutionary Biology, School of Animal Biology (M092), The University of Western Australia, Crawley 6009, WA, Australia The past two decades have seen extensive growth of characterization of genes and their effects, from DNA sexual selection research. Theoretical and empirical sequences via protein to phenotypic expression at the level work has clarified many components of pre- and of the individual, with possible consequences at the postcopulatory sexual selection, such as aggressive population level and above. competition, mate choice, sperm utilization and sexual conflict. Genetic mechanisms of mate choice evolution Evolution of mate choice have been less amenable to empirical testing, but Although mate choice occurs in males and females [4], for molecular genetic analyses can now be used for incisive convenience we refer here to female choice of male traits. experimentation. Here, we highlight some of the As experimental evidence accumulated, mate choice currently debated areas in pre- and postcopulatory became widely recognized, but the genetic mechanisms sexual selection. We identify where new techniques underlying its evolution remain the subject of debate can help estimate the relative roles of the various (Box 1). Showing how mating preferences evolve geneti- selection mechanisms that might work together in the cally is harder than showing that they exist, and the evolution of mating preferences and attractive traits, problem is aggravated by the possibility that several and in sperm–egg interactions.
    [Show full text]
  • Analysis of Host-Parasite Cospeciation: Effects of Spatial and Temporal Scale
    Louisiana State University LSU Digital Commons LSU Historical Dissertations and Theses Graduate School 1996 Analysis of Host-Parasite Cospeciation: Effects of Spatial and Temporal Scale. James W. Demastes Louisiana State University and Agricultural & Mechanical College Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_disstheses Recommended Citation Demastes, James W., "Analysis of Host-Parasite Cospeciation: Effects of Spatial and Temporal Scale." (1996). LSU Historical Dissertations and Theses. 6331. https://digitalcommons.lsu.edu/gradschool_disstheses/6331 This Dissertation is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Historical Dissertations and Theses by an authorized administrator of LSU Digital Commons. For more information, please contact [email protected]. INFORMATION TO USERS This manuscript has been reproduced from the microfilm master. UMI films the text directly from the original or copy submitted. Thus, some thesis and dissertation copies are in typewriter face, while others may be from any type o f computer printer. The quality of this reproduction is dependent upon the quality of the copy submitted. Broken or indistinct print, colored or poor quality illustrations and photographs, print bleedthrough, substandard margins, and improper alignment can adversely affect reproduction. In the unlikely event that the author did not send UMI a complete manuscript and there are missing pages, these will be noted. Also, if unauthorized copyright material had to be removed, a note will indicate the deletion. Oversize materials (e.g., maps, drawings, charts) are reproduced by sectioning the original, beginning at the upper left-hand comer and continuing from left to right in equal sections with small overlaps.
    [Show full text]