Multiple Niche Polymorphism
1972; University of Chicago Press; Volume: 106; Issue: 948 Linguagem: Inglês
10.1086/282765
ISSN1537-5323
Autores ResumoPrevious articleNext article No AccessLetters to the EditorsMultiple Niche PolymorphismM. G. BulmerM. G. BulmerPDFPDF PLUS Add to favoritesDownload CitationTrack CitationsPermissionsReprints Share onFacebookTwitterLinkedInRedditEmail SectionsMoreDetailsFiguresReferencesCited by The American Naturalist Volume 106, Number 948Mar. - Apr., 1972 Published for The American Society of Naturalists Article DOIhttps://doi.org/10.1086/282765 Views: 26Total views on this site Citations: 109Citations are reported from Crossref Copyright 1972 The University of Chicago.PDF download Crossref reports the following articles citing this article:Jakub Svoboda, Josef Tkadlec, Kamran Kaveh, Krishnendu Chatterjee Coexistence times in the Moran process with environmental heterogeneity, Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences 479, no.22712271 (Mar 2023).https://doi.org/10.1098/rspa.2022.0685Richard M. Sibly, Robert N. Curnow Sexual imprinting leads to speciation in locally adapted populations, Ecology and Evolution 12, no.1111 (Nov 2022).https://doi.org/10.1002/ece3.9479Xinghu Qin, Charleston W K Chiang, Oscar E Gaggiotti Deciphering signatures of natural selection via deep learning, Briefings in Bioinformatics 23, no.55 (Sep 2022).https://doi.org/10.1093/bib/bbac354Matteo Tomasini, Stephan Peischl The role of spatial structure in multi‐deme models of evolutionary rescue, Journal of Evolutionary Biology 35, no.77 (Jun 2022): 986–1001.https://doi.org/10.1111/jeb.14018Jitka Polechová The costs and benefits of dispersal in small populations, Philosophical Transactions of the Royal Society B: Biological Sciences 377, no.18481848 (Feb 2022).https://doi.org/10.1098/rstb.2021.0011Philippe Cubry, Sylvie Oddou‐Muratorio, Ivan Scotti, François Lefèvre Interactions between microenvironment, selection and genetic architecture drive multiscale adaptation in a simulation experiment, Journal of Evolutionary Biology 35, no.33 (Feb 2022): 451–466.https://doi.org/10.1111/jeb.13988NOËL BONNEUIL OPTIMAL CONTROL OF GENETIC DIVERSITY IN THE MORAN MODEL WITH POPULATION GROWTH, Journal of Biological Systems 30, no.0101 (Apr 2022): 27–50.https://doi.org/10.1142/S0218339022500012Bogi Trickovic, Sylvain Glémin, G Martin Establishment of local adaptation in partly self-fertilizing populations, Genetics 220, no.22 (Nov 2021).https://doi.org/10.1093/genetics/iyab201Sacha Zahnd, Amaranta Fontcuberta, Mesut Koken, Aline Cardinaux, Michel Chapuisat Fine-scale habitat heterogeneity favours the coexistence of supergene-controlled social forms in Formica selysi, BMC Ecology and Evolution 21, no.11 (Feb 2021).https://doi.org/10.1186/s12862-020-01742-0Joshua A. Thia, Katrina McGuigan, Libby Liggins, Will F. Figueira, Christopher E. Bird, Andrew Mather, Jennifer L. Evans, Cynthia Riginos Genetic and phenotypic variation exhibit both predictable and stochastic patterns across an intertidal fish metapopulation, Molecular Ecology 30, no.1818 (May 2021): 4392–4414.https://doi.org/10.1111/mec.15829Louise Brousseau, Paul V. A. Fine, Erwin Dreyer, Giovanni G. Vendramin, Ivan Scotti Genomic and phenotypic divergence unveil microgeographic adaptation in the Amazonian hyperdominant tree Eperua falcata Aubl. (Fabaceae), Molecular Ecology 30, no.55 (Sep 2020): 1136–1154.https://doi.org/10.1111/mec.15595Sergio Tusso, Bart P. S. Nieuwenhuis, Bernadette Weissensteiner, Simone Immler, Jochen B. W. Wolf Experimental evolution of adaptive divergence under varying degrees of gene flow, Nature Ecology & Evolution 5, no.33 (Jan 2021): 338–349.https://doi.org/10.1038/s41559-020-01363-2Nathan C. Layman, Beth M. Tuschhoff, Andrew J. Basinski, Christopher H. Remien, James J. Bull, Scott L. Nuismer Suppressing evolution in genetically engineered systems through repeated supplementation, Evolutionary Applications 14, no.22 (Nov 2020): 348–359.https://doi.org/10.1111/eva.13119Maria R. Servedio, Reinhard Bürger The effectiveness of pseudomagic traits in promoting divergence and enhancing local adaptation*, Evolution 74, no.1111 (Aug 2020): 2438–2450.https://doi.org/10.1111/evo.14056Gabriel A. Jamie, Joana I. Meier The Persistence of Polymorphisms across Species Radiations, Trends in Ecology & Evolution 35, no.99 (Sep 2020): 795–808.https://doi.org/10.1016/j.tree.2020.04.007Matteo Tomasini, Stephan Peischl When does gene flow facilitate evolutionary rescue?, Evolution 74, no.88 (Jun 2020): 1640–1653.https://doi.org/10.1111/evo.14038Judith C. Bachmann, Alexandra Jansen van Rensburg, Maria Cortazar-Chinarro, Anssi Laurila, and Josh Van Buskirk Gene Flow Limits Adaptation along Steep Environmental Gradients, The American Naturalist 195, no.33 (Jan 2020): E67–E86.https://doi.org/10.1086/707209Maria R. Servedio, Joachim Hermisson The evolution of partial reproductive isolation as an adaptive optimum, Evolution 74, no.11 (Nov 2019): 4–14.https://doi.org/10.1111/evo.13880Margaux-Alison Fustier, Natalia E. Martínez-Ainsworth, Jonás A. Aguirre-Liguori, Anthony Venon, Hélène Corti, Agnès Rousselet, Fabrice Dumas, Hannes Dittberner, María G. Camarena, Daniel Grimanelli, Otso Ovaskainen, Matthieu Falque, Laurence Moreau, Juliette de Meaux, Salvador Montes-Hernández, Luis E. Eguiarte, Yves Vigouroux, Domenica Manicacci, Maud I. Tenaillon, Martin Lascoux Common gardens in teosintes reveal the establishment of a syndrome of adaptation to altitude, PLOS Genetics 15, no.1212 (Dec 2019): e1008512.https://doi.org/10.1371/journal.pgen.1008512Pascal Milesi, Mats Berlin, Jun Chen, Marion Orsucci, Lili Li, Gunnar Jansson, Bo Karlsson, Martin Lascoux Assessing the potential for assisted gene flow using past introduction of Norway spruce in southern Sweden: Local adaptation and genetic basis of quantitative traits in trees, Evolutionary Applications 12, no.1010 (Aug 2019): 1946–1959.https://doi.org/10.1111/eva.12855Hanja Pisa, Joachim Hermisson, Jitka Polechová The influence of fluctuating population densities on evolutionary dynamics, Evolution 73, no.77 (Jun 2019): 1341–1355.https://doi.org/10.1111/evo.13756Todd W. Pierson, Jennifer Deitloff, Stanley K. Sessions, Kenneth H. Kozak, and Benjamin M. Fitzpatrick Morphological Polymorphism Associated with Alternative Reproductive Tactics in a Plethodontid Salamander, The American Naturalist 193, no.44 (Mar 2019): 608–618.https://doi.org/10.1086/702251Joanna L. Rifkin, Allan S. Castillo, Irene T. Liao, Mark D. Rausher Gene flow, divergent selection and resistance to introgression in two species of morning glories ( Ipomoea ), Molecular Ecology 28, no.77 (Apr 2019): 1709–1729.https://doi.org/10.1111/mec.14945Tuomas Hämälä, Tiina M. Mattila, Outi Savolainen Local adaptation and ecological differentiation under selection, migration, and drift in Arabidopsis lyrata *, Evolution 72, no.77 (May 2018): 1373–1386.https://doi.org/10.1111/evo.13502Matteo Tomasini, Stephan Peischl Establishment of Locally Adapted Mutations Under Divergent Selection, Genetics (May 2018): genetics.301104.2018.https://doi.org/10.1534/genetics.118.301104Reed A. Cartwright, Rachel S. Schwartz, Alexandra L. Merry, Megan M. Howell The importance of selection in the evolution of blindness in cavefish, BMC Evolutionary Biology 17, no.11 (Feb 2017).https://doi.org/10.1186/s12862-017-0876-4Susana M. Wadgymar, David B. Lowry, Billie A. Gould, Caitlyn N. Byron, Rachel M. Mactavish, Jill T. Anderson, John Stinchcombe Identifying targets and agents of selection: innovative methods to evaluate the processes that contribute to local adaptation, Methods in Ecology and Evolution 8, no.66 (Jun 2017): 738–749.https://doi.org/10.1111/2041-210X.12777Pierre-Alexandre Gagnaire, Oscar E. Gaggiotti Detecting polygenic selection in marine populations by combining population genomics and quantitative genetics approaches, Current Zoology 62, no.66 (Aug 2016): 603–616.https://doi.org/10.1093/cz/zow088Jeffrey W. Streicher, Jay P. McEntee, Laura C. Drzich, Daren C. Card, Drew R. Schield, Utpal Smart, Christopher L. Parkinson, Tereza Jezkova, Eric N. Smith, Todd A. Castoe Genetic surfing, not allopatric divergence, explains spatial sorting of mitochondrial haplotypes in venomous coralsnakes, Evolution 70, no.77 (Jun 2016): 1435–1449.https://doi.org/10.1111/evo.12967Timothy H. Vines, Anne C. Dalziel, Arianne Y. K. Albert, Thor Veen, Patricia M. Schulte, Dolph Schluter Cline coupling and uncoupling in a stickleback hybrid zone, Evolution 70, no.55 (Apr 2016): 1023–1038.https://doi.org/10.1111/evo.12917Martin Lascoux, Sylvain Glémin, Outi Savolainen Local Adaptation in Plants, (Feb 2016): 1–7.https://doi.org/10.1002/9780470015902.a0025270Sam Yeaman Local Adaptation by Alleles of Small Effect, The American Naturalist 186, no.S1S1 (Nov 2015): S74–S89.https://doi.org/10.1086/682405Michael C. Whitlock Modern Approaches to Local Adaptation, The American Naturalist 186, no.S1S1 (Nov 2015): S1–S4.https://doi.org/10.1086/682933Thomas Nagylaki Dying on the way: The influence of migrational mortality on clines, Theoretical Population Biology 101 (May 2015): 54–60.https://doi.org/10.1016/j.tpb.2015.02.005Xinzhu Wei, Lei Zhao, Martin Lascoux, David Waxman Population structure and the rate of evolution, Journal of Theoretical Biology 365 (Jan 2015): 486–495.https://doi.org/10.1016/j.jtbi.2014.10.041Tami E. Cruickshank, Matthew W. Hahn Reanalysis suggests that genomic islands of speciation are due to reduced diversity, not reduced gene flow, Molecular Ecology 23, no.1313 (Jun 2014): 3133–3157.https://doi.org/10.1111/mec.12796Ada Akerman, Reinhard Bürger The consequences of dominance and gene flow for local adaptation and differentiation at two linked loci, Theoretical Population Biology 94 (Jun 2014): 42–62.https://doi.org/10.1016/j.tpb.2014.04.001Reinhard Bürger A survey of migration-selection models in population genetics, Discrete and Continuous Dynamical Systems - Series B 19, no.44 (Apr 2014): 883–959.https://doi.org/10.3934/dcdsb.2014.19.883Elizabeth C. Bourne, Greta Bocedi, Justin M. J. Travis, Robin J. Pakeman, Rob W. Brooker, Katja Schiffers Between migration load and evolutionary rescue: dispersal, adaptation and the response of spatially structured populations to environmental change, Proceedings of the Royal Society B: Biological Sciences 281, no.17781778 (Mar 2014): 20132795.https://doi.org/10.1098/rspb.2013.2795Outi Savolainen, Martin Lascoux, Juha Merilä Ecological genomics of local adaptation, Nature Reviews Genetics 14, no.1111 (Oct 2013): 807–820.https://doi.org/10.1038/nrg3522A. Paccard, M. Vance, Y. Willi Weak impact of fine-scale landscape heterogeneity on evolutionary potential in Arabidopsis lyrata, Journal of Evolutionary Biology 26, no.1111 (Aug 2013): 2331–2340.https://doi.org/10.1111/jeb.12220P. Nouvellet, S. Gourbière Biased sex-ratio and sex-biased heterozygote disadvantage affect the maintenance of a genetic polymorphism and the properties of hybrid zones, Journal of Evolutionary Biology 26, no.88 (Jul 2013): 1774–1783.https://doi.org/10.1111/jeb.12180Rose L. Andrew, Nolan C. Kane, Greg J. Baute, Christopher J. Grassa, Loren H. Rieseberg Recent nonhybrid origin of sunflower ecotypes in a novel habitat, Molecular Ecology 22, no.33 (Oct 2012): 799–813.https://doi.org/10.1111/mec.12038Beate Nürnberger Ecological Genetics, (Jan 2013): 714–731.https://doi.org/10.1016/B978-0-12-384719-5.00038-1Christina Zakas, David W. Hall Asymmetric Dispersal Can Maintain Larval Polymorphism: A Model Motivated by Streblospio benedicti, Integrative and Comparative Biology 52, no.11 (May 2012): 197–212.https://doi.org/10.1093/icb/ics055Thomas Nagylaki Clines with partial panmixia, Theoretical Population Biology 81, no.11 (Feb 2012): 45–68.https://doi.org/10.1016/j.tpb.2011.09.006Noël Bonneuil Multiallelic polymorphism maintained under unpredictable migration and selection, Journal of Theoretical Biology 293 (Jan 2012): 189–196.https://doi.org/10.1016/j.jtbi.2011.09.027Benjamin M. Fitzpatrick Underappreciated Consequences of Phenotypic Plasticity for Ecological Speciation, International Journal of Ecology 2012 (Jan 2012): 1–12.https://doi.org/10.1155/2012/256017Ângela M. Ribeiro, Penn Lloyd, Rauri C. K. Bowie A TIGHT BALANCE BETWEEN NATURAL SELECTION AND GENE FLOW IN A SOUTHERN AFRICAN ARID-ZONE ENDEMIC BIRD, Evolution 65, no.1212 (Jul 2011): 3499–3514.https://doi.org/10.1111/j.1558-5646.2011.01397.xMark C. Urban The evolution of species interactions across natural landscapes, Ecology Letters 14, no.77 (May 2011): 723–732.https://doi.org/10.1111/j.1461-0248.2011.01632.xSam Yeaman, Michael C. Whitlock THE GENETIC ARCHITECTURE OF ADAPTATION UNDER MIGRATION-SELECTION BALANCE, Evolution 65, no.77 (Mar 2011): 1897–1911.https://doi.org/10.1111/j.1558-5646.2011.01269.xSam Yeaman, Sarah P. Otto ESTABLISHMENT AND MAINTENANCE OF ADAPTIVE GENETIC DIVERGENCE UNDER MIGRATION, SELECTION, AND DRIFT, Evolution 65, no.77 (Mar 2011): 2123–2129.https://doi.org/10.1111/j.1558-5646.2011.01277.xFrédéric Guillaume MIGRATION-INDUCED PHENOTYPIC DIVERGENCE: THE MIGRATION-SELECTION BALANCE OF CORRELATED TRAITS, Evolution 65, no.66 (Mar 2011): 1723–1738.https://doi.org/10.1111/j.1558-5646.2011.01248.xAurélien Tellier, James KM Brown Spatial heterogeneity, frequency-dependent selection and polymorphism in host-parasite interactions, BMC Evolutionary Biology 11, no.11 (Jan 2011): 319.https://doi.org/10.1186/1471-2148-11-319Sergei Volis, Yong-Hong Zhang Separating Effects of Gene Flow and Natural Selection along an Environmental Gradient, Evolutionary Biology 37, no.44 (Oct 2010): 187–199.https://doi.org/10.1007/s11692-010-9095-2Virginie Ravigné, Ulf Dieckmann, and Isabelle Olivieri Live Where You Thrive: Joint Evolution of Habitat Choice and Local Adaptation Facilitates Specialization and Promotes Diversity. V. Ravigné et al., The American Naturalist 174, no.44 (Jul 2015): E141–E169.https://doi.org/10.1086/605369Daniel I. Bolnick, Lisa K. Snowberg, Claire Patenia, William E. Stutz, Travis Ingram, On Lee Lau PHENOTYPE-DEPENDENT NATIVE HABITAT PREFERENCE FACILITATES DIVERGENCE BETWEEN PARAPATRIC LAKE AND STREAM STICKLEBACK, Evolution 63, no.88 (Aug 2009): 2004–2016.https://doi.org/10.1111/j.1558-5646.2009.00699.xReinhard Bürger Multilocus selection in subdivided populations I. Convergence properties for weak or strong migration, Journal of Mathematical Biology 58, no.66 (Nov 2008): 939–978.https://doi.org/10.1007/s00285-008-0236-5Reinhard Bürger Multilocus selection in subdivided populations II. Maintenance of polymorphism under weak or strong migration, Journal of Mathematical Biology 58, no.66 (Nov 2008): 979–997.https://doi.org/10.1007/s00285-008-0237-4Thomas Nagylaki Polymorphism in multiallelic migration–selection models with dominance, Theoretical Population Biology 75, no.44 (Jun 2009): 239–259.https://doi.org/10.1016/j.tpb.2009.01.004Zachary A. Cheviron, Robb T. Brumfield MIGRATION-SELECTION BALANCE AND LOCAL ADAPTATION OF MITOCHONDRIAL HAPLOTYPES IN RUFOUS-COLLARED SPARROWS ( ZONOTRICHIA CAPENSIS ) ALONG AN ELEVATIONAL GRADIENT, Evolution 63, no.66 (Jun 2009): 1593–1605.https://doi.org/10.1111/j.1558-5646.2009.00644.xPATRIK NOSIL, DANIEL J. FUNK, DANIEL ORTIZ-BARRIENTOS Divergent selection and heterogeneous genomic divergence, Molecular Ecology 18, no.33 (Feb 2009): 375–402.https://doi.org/10.1111/j.1365-294X.2008.03946.xB. M. FITZPATRICK, J. A. FORDYCE, S. GAVRILETS What, if anything, is sympatric speciation?, Journal of Evolutionary Biology 21, no.66 (Nov 2008): 1452–1459.https://doi.org/10.1111/j.1420-9101.2008.01611.xPATRIK NOSIL Ernst Mayr and the integration of geographic and ecological factors in speciation, Biological Journal of the Linnean Society 95, no.11 (Sep 2008): 26–46.https://doi.org/10.1111/j.1095-8312.2008.01091.xBENJAMIN M. FITZPATRICK, JOHN S. PLACYK, JR, MATTHEW L. NIEMILLER, GARY S. CASPER, GORDON M. BURGHARDT Distinctiveness in the face of gene flow: hybridization between specialist and generalist gartersnakes, Molecular Ecology 17, no.1818 (Sep 2008): 4107–4117.https://doi.org/10.1111/j.1365-294X.2008.03885.xDANIEL I. BOLNICK, ERIC J. CALDERA, BLAKE MATTHEWS Evidence for asymmetric migration load in a pair of ecologically divergent stickleback populations, Biological Journal of the Linnean Society 94, no.22 (May 2008): 273–287.https://doi.org/10.1111/j.1095-8312.2008.00978.xT. Nagylaki, Y. Lou The Dynamics of Migration–Selection Models, (Jan 2008): 117–170.https://doi.org/10.1007/978-3-540-74331-6_4Bastiaan Star, Rick J. Stoffels, Hamish G. Spencer Evolution of Fitnesses and Allele Frequencies in a Population With Spatially Heterogeneous Selection Pressures, Genetics 177, no.33 (Oct 2007): 1743–1751.https://doi.org/10.1534/genetics.107.079558Daniel I. Bolnick, Patrik Nosil NATURAL SELECTION IN POPULATIONS SUBJECT TO A MIGRATION LOAD, Evolution 61, no.99 (Sep 2007): 2229–2243.https://doi.org/10.1111/j.1558-5646.2007.00179.xBastiaan Star, Rick J Stoffels, Hamish G Spencer Single-Locus Polymorphism in a Heterogeneous Two-Deme Model, Genetics 176, no.33 (Jul 2007): 1625–1633.https://doi.org/10.1534/genetics.107.071639Mark C. Urban, David K. Skelly EVOLVING METACOMMUNITIES: TOWARD AN EVOLUTIONARY PERSPECTIVE ON METACOMMUNITIES, Ecology 87, no.77 (Jul 2006): 1616–1626.https://doi.org/10.1890/0012-9658(2006)87[1616:EMTAEP]2.0.CO;2C K Griswold Gene flow's effect on the genetic architecture of a local adaptation and its consequences for QTL analyses, Heredity 96, no.66 (Apr 2006): 445–453.https://doi.org/10.1038/sj.hdy.6800822D. VELIZ, P. DUCHESNE, E. BOURGET, L. BERNATCHEZ Stable genetic polymorphism in heterogeneous environments: balance between asymmetrical dispersal and selection in the acorn barnacle, Journal of Evolutionary Biology 19, no.22 (Mar 2006): 589–599.https://doi.org/10.1111/j.1420-9101.2005.01000.xSylvain Billiard, Thomas Lenormand EVOLUTION OF MIGRATION UNDER KIN SELECTION AND LOCAL ADAPTATION, Evolution 59, no.11 (Jan 2005): 13–23.https://doi.org/10.1111/j.0014-3820.2005.tb00890.xPaul Gepts, Roberto Papa Possible effects of (trans)gene flow from crops on the genetic diversity from landraces and wild relatives, Environmental Biosafety Research 2, no.22 (Jun 2003): 89–103.https://doi.org/10.1051/ebr:2003009Thomas Nagylaki, Yuan Lou Patterns of Multiallelic Polymorphism Maintained by Migration and Selection, Theoretical Population Biology 59, no.44 (Jun 2001): 297–313.https://doi.org/10.1006/tpbi.2001.1526Graham Bell The poverty of the protists, (Jan 2001): 46–58.https://doi.org/10.1017/CBO9780511815683.005C. Dytham, B. Shorrocks Selection, patches and genetic variation: A cellular automaton modellingDrosophila populations, Evolutionary Ecology 6, no.44 (Jul 1992): 342–351.https://doi.org/10.1007/BF02270970O. Halkka, M. Raatikainen, L. Halkka Conditions requisite for stability of polymorphic balance in Philaenus spumarius (L.) (Homoptera), Genetica 46, no.11 (Sep 1990): 67–76.https://doi.org/10.1007/BF00122518Bryan Shorrocks Competition and Selection in a Patchy and Ephemeral Habitat: The Implications for Insect Life-Cycles, (Jan 1990): 215–228.https://doi.org/10.1007/978-1-4471-3464-0_15 Freddy Bugge Christiansen Selection and Population Regulation with Habitat Variation, The American Naturalist 126, no.33 (Oct 2015): 418–429.https://doi.org/10.1086/284427 Michael J. Wade Soft Selection, Hard Selection, Kin Selection, and Group Selection, The American Naturalist 125, no.11 (Oct 2015): 61–73.https://doi.org/10.1086/284328 James Bruce Walsh Hard Lessons for Soft Selection, The American Naturalist 124, no.44 (Oct 2015): 518–526.https://doi.org/10.1086/284291James Bruce Walsh Conditions for protection of an allele in linear homogeneous stepping stone models, Theoretical Population Biology 24, no.11 (Aug 1983): 78–106.https://doi.org/10.1016/0040-5809(83)90047-3R. B. Campbell The effect of variable environments on polymorphism at loci with several alleles II. Submultiplicative viabilities, Journal of Mathematical Biology 15, no.33 (Nov 1982): 293–303.https://doi.org/10.1007/BF00275689Joel E. Cohen, Shmuel Friedland, Tosio Kato, Frank P. Kelly Eigenvalue inequalities for products of matrix exponentials, Linear Algebra and its Applications 45 (Jun 1982): 55–95.https://doi.org/10.1016/0024-3795(82)90211-7R.B. Campbell Hard selection in haploid species, Theoretical Population Biology 21, no.11 (Feb 1982): 1–10.https://doi.org/10.1016/0040-5809(82)90002-8W. D. Hamilton Pathogens as Causes of Genetic Diversity in their Host Populations, (Jan 1982): 269–296.https://doi.org/10.1007/978-3-642-68635-1_14R. B. Campbell The effect of variable environments on polymorphism at loci with several alleles I. A symmetric model, Journal of Mathematical Biology 13, no.22 (Dec 1981): 199–208.https://doi.org/10.1007/BF00275214R.B. Campbell Some circumstances assuring monomorphism in subdivided populations, Theoretical Population Biology 20, no.11 (Aug 1981): 118–125.https://doi.org/10.1016/0040-5809(81)90006-XMichael Moody Polymorphism with selection and genotype-dependent migration, Journal of Mathematical Biology 11, no.33 (Mar 1981): 245–267.https://doi.org/10.1007/BF00276896Samuel Karlin, R B Campbell Polymorphism in subdivided populations characterised by a major and subordinate demes, Heredity 44, no.22 (Apr 1980): 151–168.https://doi.org/10.1038/hdy.1980.13Timothy Prout Some Relationships between Density-Independent Selection and Density-Dependent Population Growth, (Jan 1980): 1–68.https://doi.org/10.1007/978-1-4615-6962-6_1 Evelyn P. Ewing Genetic Variation in a Heterogeneous Environment VII. Temporal and Spatial Heterogeneity in Infinite Populations, The American Naturalist 114, no.22 (Oct 2015): 197–212.https://doi.org/10.1086/283468Thomas Nagylaki Migration-selection polymorphism in dioecious populations, Journal of Mathematical Biology 8, no.22 (Jan 1979): 123–131.https://doi.org/10.1007/BF00279716Michael Moody Polymorphism with migration and selection, Journal of Mathematical Biology 8, no.11 (Jan 1979): 73–109.https://doi.org/10.1007/BF00280587P.J. Avery Selection effects in a model of two intermigrating colonies of finite size, Theoretical Population Biology 13, no.11 (Feb 1978): 24–39.https://doi.org/10.1016/0040-5809(78)90034-5 Samuel Karlin Protection of Recessive and Dominant Traits in a Subdivided Population with General Migration Structure, The American Naturalist 111, no.982982 (Oct 2015): 1145–1162.https://doi.org/10.1086/283242James A. Scott, G.A.H. McClelland A model of polymorphism with several seasons and several habitats, and its application to the mosquito Aedes aegypti, Theoretical Population Biology 11, no.33 (Jun 1977): 342–355.https://doi.org/10.1016/0040-5809(77)90017-XSamuel Karlin, Ron S. Kenett Variable spatial selection with two stages of migrations and comparisons between different timings, Theoretical Population Biology 11, no.33 (Jun 1977): 386–409.https://doi.org/10.1016/0040-5809(77)90019-3Olli Halkka, Erkki Mikkola The Selection Regime of Philaenus Spumarius (L.) (Homoptera), (Jan 1977): 445–463.https://doi.org/10.1007/978-3-642-93071-3_26 Roger W. Doyle Analysis of Habitat Loyalty and Habitat Preference in the Settlement Behavior of Planktonic Marine Larvae, The American Naturalist 110, no.975975 (Oct 2015): 719–730.https://doi.org/10.1086/283099Thomas Nagylaki Dispersion-selection balance in localised plant populations, Heredity 37, no.11 (Aug 1976): 59–67.https://doi.org/10.1038/hdy.1976.65Edwin H. Bryant A COMMENT ON THE ROLE OF ENVIRONMENTAL VARIATION IN MAINTAINING POLYMORPHISMS IN NATURAL POPULATIONS, Evolution 30, no.11 (May 2017): 188–190.https://doi.org/10.1111/j.1558-5646.1976.tb00897.xS. KARLIN Population Subdivision and Selection Migration Interaction**Research supported in part by National Institutes of Health Grant USPHS 10452-12 and NSF Grant No. MPS71-02905 A03., (Jan 1976): 617–657.https://doi.org/10.1016/B978-0-12-398560-6.50033-XFreddy Bugge Christiansen, Marcus W. Feldman Subdivided populations: A review of the one- and two-locus deterministic theory, Theoretical Population Biology 7, no.11 (Feb 1975): 13–38.https://doi.org/10.1016/0040-5809(75)90003-9 Freddy Bugge Christiansen Hard and Soft Selection in a Subdivided Population, The American Naturalist 109, no.965965 (Oct 2015): 11–16.https://doi.org/10.1086/282970 Freddy Bugge Christiansen Sufficient Conditions for Protected Polymorphism in a Subdivided Population, The American Naturalist 108, no.960960 (Oct 2015): 157–166.https://doi.org/10.1086/282896 Edwin H. Bryant On the Adaptive Significance of Enzyme Polymorphisms in Relation to Environmental Variability, The American Naturalist 108, no.959959 (Oct 2015): 1–19.https://doi.org/10.1086/282881
Referência(s)