Differentiation of Allelic Frequencies at Quantitative Trait Loci Affecting Locally Adaptive Traits
1998; University of Chicago Press; Volume: 151; Issue: 3 Linguagem: Inglês
10.2307/2463350
ISSN1537-5323
Autores Tópico(s)Agriculture, Soil, Plant Science
ResumoPrevious article No AccessDifferentiation of Allelic Frequencies at Quantitative Trait Loci Affecting Locally Adaptive TraitsRobert G. LattaRobert G. LattaDepartment of Environmental, Population and Organismic Biology, University of Colorado, Boulder, Colorado 80309–0334 Search for more articles by this author Department of Environmental, Population and Organismic Biology, University of Colorado, Boulder, Colorado 80309–0334PDFPDF PLUS Add to favoritesDownload CitationTrack CitationsPermissionsReprints Share onFacebookTwitterLinkedInRedditEmail SectionsMoreDetailsFiguresReferencesCited by The American Naturalist Volume 151, Number 3March 1998 Published for The American Society of Naturalists Article DOIhttps://doi.org/10.1086/286119 Views: 109Total views on this site Citations: 136Citations are reported from Crossref HistoryReceived May 5, 1997Accepted September 10, 1997 Keywordsquantitative trait locilinkage disequilibriummultilocus differentiationlocal adaptation© 1998 by The University of Chicago.PDF download Crossref reports the following articles citing this article:Sanna Olsson, Benjamin Dauphin, Véronique Jorge, Delphine Grivet, Anna Maria Farsakoglou, Jose Climent, Paraskevi Alizoti, Patricia Faivre-Rampant, Sara Pinosio, Pascal Milesi, Simone Scalabrin, Francesca Bagnoli, Ivan Scotti, Giovanni G. 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González‐Martínez Polygenic adaptation and negative selection across traits, years and environments in a long‐lived plant species ( Pinus pinaster Ait., Pinaceae), Molecular Ecology 31, no.77 (Feb 2022): 2089–2105.https://doi.org/10.1111/mec.16367Philippe 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.13988Quiterie Haenel, Laurent Guerard, Andrew D. C. MacColl, Daniel Berner The maintenance of standing genetic variation: Gene flow vs. selective neutrality in Atlantic stickleback fish, Molecular Ecology 31, no.33 (Nov 2021): 811–821.https://doi.org/10.1111/mec.16269Sam Yeaman Evolution of polygenic traits under global vs local adaptation, Genetics 220, no.11 (Jan 2022).https://doi.org/10.1093/genetics/iyab134Carole M. Smadja, Etienne Loire, Pierre Caminade, Dany Severac, Mathieu Gautier, Guila Ganem Divergence of olfactory receptors associated with the evolution of assortative mating and reproductive isolation in mice, Peer Community Journal 2 (Nov 2022).https://doi.org/10.24072/pcjournal.190Maud Fagny, Frédéric Austerlitz Polygenic Adaptation: Integrating Population Genetics and Gene Regulatory Networks, Trends in Genetics 37, no.77 (Jul 2021): 631–638.https://doi.org/10.1016/j.tig.2021.03.005Moritz A Ehrlich, Dominique N Wagner, Marjorie F Oleksiak, Douglas L Crawford, Bonnie Fraser Polygenic Selection within a Single Generation Leads to Subtle Divergence among Ecological Niches, Genome Biology and Evolution 13, no.22 (Dec 2020).https://doi.org/10.1093/gbe/evaa257Elizabeth A. Werren, Obed Garcia, Abigail W. Bigham Identifying adaptive alleles in the human genome: from selection mapping to functional validation, Human Genetics 140, no.22 (Jul 2020): 241–276.https://doi.org/10.1007/s00439-020-02206-7David Hall, Jenny Olsson, Wei Zhao, Johan Kroon, Ulfstand Wennström, Xiao-Ru Wang Divergent patterns between phenotypic and genetic variation in Scots pine, Plant Communications 2, no.11 (Jan 2021): 100139.https://doi.org/10.1016/j.xplc.2020.100139Telma G. Laurentino, Dario Moser, Marius Roesti, Matthias Ammann, Anja Frey, Fabrizia Ronco, Benjamin Kueng, Daniel Berner Genomic release-recapture experiment in the wild reveals within-generation polygenic selection in stickleback fish, Nature Communications 11, no.11 (Apr 2020).https://doi.org/10.1038/s41467-020-15657-3Tom R. Booker, Sam Yeaman, Michael C. Whitlock Variation in recombination rate affects detection of outliers in genome scans under neutrality, Molecular Ecology 29, no.2222 (Jul 2020): 4274–4279.https://doi.org/10.1111/mec.15501Vince Buffalo, Graham Coop Estimating the genome-wide contribution of selection to temporal allele frequency change, Proceedings of the National Academy of Sciences 117, no.3434 (Aug 2020): 20672–20680.https://doi.org/10.1073/pnas.1919039117Jaakko S Tyrmi, Jaana Vuosku, Juan J Acosta, Zhen Li, Lieven Sterck, Maria T Cervera, Outi Savolainen, Tanja Pyhäjärvi Genomics of Clinal Local Adaptation in Pinus sylvestris Under Continuous Environmental and Spatial Genetic Setting, G3 Genes|Genomes|Genetics 10, no.88 (Aug 2020): 2683–2696.https://doi.org/10.1534/g3.120.401285H. Nickolas, D. Williams, G. Downes, P. A. Harrison, R. E. Vaillancourt, B. M. Potts Application of resistance drilling to genetic studies of growth, wood basic density and bark thickness in Eucalyptus globulus, Australian Forestry 83, no.33 (Sep 2020): 172–179.https://doi.org/10.1080/00049158.2020.1808276Henry Nickolas, Dean Williams, Geoff Downes, Paul Tilyard, Peter A. Harrison, René E. Vaillancourt, Brad Potts Genetic correlations among pulpwood and solid-wood selection traits in Eucalyptus globulus, New Forests 51, no.11 (May 2019): 137–158.https://doi.org/10.1007/s11056-019-09721-0Tanja Pyhäjärvi, Sonja T Kujala, Outi Savolainen 275 years of forestry meets genomics in Pinus sylvestris, Evolutionary Applications 13, no.11 (Jun 2019): 11–30.https://doi.org/10.1111/eva.12809Tuomas Hämälä, Outi Savolainen Genomic Patterns of Local Adaptation under Gene Flow in Arabidopsis lyrata, Molecular Biology and Evolution 36, no.1111 (Jun 2019): 2557–2571.https://doi.org/10.1093/molbev/msz149Amanda R De La Torre, Benjamin Wilhite, David B Neale, Tanja Slotte Environmental Genome-Wide Association Reveals Climate Adaptation Is Shaped by Subtle to Moderate Allele Frequency Shifts in Loblolly Pine, Genome Biology and Evolution 11, no.1010 (Oct 2019): 2976–2989.https://doi.org/10.1093/gbe/evz220Pär K. Ingvarsson, Helena Dahlberg The effects of clonal forestry on genetic diversity in wild and domesticated stands of forest trees, Scandinavian Journal of Forest Research 34, no.55 (May 2018): 370–379.https://doi.org/10.1080/02827581.2018.1469665Jules S. Freeman, Matthew G. Hamilton, David J. Lee, Geoff S. Pegg, Jeremy T. Brawner, Paul A. Tilyard, Brad M. Potts Comparison of host susceptibilities to native and exotic pathogens provides evidence for pathogen‐imposed selection in forest trees, New Phytologist 221, no.44 (Nov 2018): 2261–2272.https://doi.org/10.1111/nph.15557Emily B Josephs, Jeremy J Berg, Jeffrey Ross-Ibarra, Graham Coop Detecting Adaptive Differentiation in Structured Populations with Genomic Data and Common Gardens, Genetics 211, no.33 (Jan 2019): 989–1004.https://doi.org/10.1534/genetics.118.301786Quiterie Haenel, Marius Roesti, Dario Moser, Andrew D. C. MacColl, Daniel Berner Predictable genome-wide sorting of standing genetic variation during parallel adaptation to basic versus acidic environments in stickleback fish, Evolution Letters 3, no.11 (Jan 2019): 28–42.https://doi.org/10.1002/evl3.99Jean‐Paul Soularue, Armel Thöni, Léo Arnoux, Valérie Le Corre, Antoine Kremer Metapop: An individual‐based model for simulating the evolution of tree populations in spatially and temporally heterogeneous landscapes, Molecular Ecology Resources 19, no.11 (Dec 2018): 296–305.https://doi.org/10.1111/1755-0998.12958Frédéric Austerlitz, Evelyne Heyer, Sudhir Kumar Neutral Theory: From Complex Population History to Natural Selection and Sociocultural Phenomena in Human Populations, Molecular Biology and Evolution 35, no.66 (Apr 2018): 1304–1307.https://doi.org/10.1093/molbev/msy067Brandon M. Lind, Mitra Menon, Constance E. Bolte, Trevor M. Faske, Andrew J. Eckert The genomics of local adaptation in trees: are we out of the woods yet?, Tree Genetics & Genomes 14, no.22 (Mar 2018).https://doi.org/10.1007/s11295-017-1224-yDaiki Takahashi, Tsutomu Teramine, Shota Sakaguchi, Hiroaki Setoguchi Relative contributions of neutral and non-neutral processes to clinal variation in calyx lobe length in the series Sakawanum (Asarum: Aristolochiaceae), Annals of Botany 121, no.11 (Nov 2017): 37–46.https://doi.org/10.1093/aob/mcx122Mariet Jose, R. Dinesh Raj, M. R. Vinitha, Remya Madhu, George Varghese, Jan Bocianowski, Rashmi Yadav, B. C. Patra, O. N. Singh, J. C. Rana, S. Leena Kurmari, George Thomas , Frontiers in Plant Science 9 ( 2018).https://doi.org/10.3389/fpls.2018.01203Philippe Cubry, Ivan Scotti, Sylvie Oddou-Muratorio, François Lefèvre Generalization of the QST framework in hierarchically structured populations: Impacts of inbreeding and dominance, Molecular Ecology Resources 17, no.66 (Aug 2017): e76–e83.https://doi.org/10.1111/1755-0998.12693Brandon M. Lind, Christopher J. Friedline, Jill L. Wegrzyn, Patricia E. Maloney, Detlev R. Vogler, David B. Neale, Andrew J. Eckert Water availability drives signatures of local adaptation in whitebark pine ( Pinus albicaulis Engelm.) across fine spatial scales of the Lake Tahoe Basin, USA, Molecular Ecology 26, no.1212 (May 2017): 3168–3185.https://doi.org/10.1111/mec.14106Rachael A. Bay, Noah Rose, Rowan Barrett, Louis Bernatchez, Cameron K. Ghalambor, Jesse R. Lasky, Rachel B. Brem, Stephen R. Palumbi, and Peter Ralph Predicting Responses to Contemporary Environmental Change Using Evolutionary Response Architectures, The American Naturalist 189, no.55 (Mar 2017): 463–473.https://doi.org/10.1086/691233Emily B. Josephs, John R. Stinchcombe, Stephen I. Wright What can genome‐wide association studies tell us about the evolutionary forces maintaining genetic variation for quantitative traits?, New Phytologist 214, no.11 (Feb 2017): 21–33.https://doi.org/10.1111/nph.14410Hanne De Kort, Olivier Honnay Assessing Evolutionary Potential in Tree Species Through Ecology-Informed Genome Screening, (Aug 2017): 313–327.https://doi.org/10.1007/978-3-319-61569-1_17Billie A. Gould, John R. Stinchcombe Population genomic scans suggest novel genes underlie convergent flowering time evolution in the introduced range of Arabidopsis thaliana, Molecular Ecology 26, no.11 (Aug 2016): 92–106.https://doi.org/10.1111/mec.13643S U Franssen, R Kofler, C Schlötterer Uncovering the genetic signature of quantitative trait evolution with replicated time series data, Heredity 118, no.11 (Nov 2016): 42–51.https://doi.org/10.1038/hdy.2016.98Simon Nadeau, Patrick G. Meirmans, Sally N. Aitken, Kermit Ritland, Nathalie Isabel The challenge of separating signatures of local adaptation from those of isolation by distance and colonization history: The case of two white pines, Ecology and Evolution 6, no.2424 (Oct 2016): 8649–8664.https://doi.org/10.1002/ece3.2550David Hall, Henrik R. Hallingbäck, Harry X. Wu Estimation of number and size of QTL effects in forest tree traits, Tree Genetics & Genomes 12, no.66 (Nov 2016).https://doi.org/10.1007/s11295-016-1073-0Asher D. Cutter, Jeremy C. Gray Ephemeral ecological speciation and the latitudinal biodiversity gradient, Evolution 70, no.1010 (Aug 2016): 2171–2185.https://doi.org/10.1111/evo.13030Sean Hoban, Joanna L. Kelley, Katie E. Lotterhos, Michael F. Antolin, Gideon Bradburd, David B. Lowry, Mary L. Poss, Laura K. Reed, Andrew Storfer, and Michael C. Whitlock Finding the Genomic Basis of Local Adaptation: Pitfalls, Practical Solutions, and Future Directions, The American Naturalist 188, no.44 (Aug 2016): 379–397.https://doi.org/10.1086/688018Om P. Rajora, Andrew J. Eckert, John W. R. Zinck, Berthold Heinze Single-Locus versus Multilocus Patterns of Local Adaptation to Climate in Eastern White Pine (Pinus strobus, Pinaceae), PLOS ONE 11, no.77 (Jul 2016): e0158691.https://doi.org/10.1371/journal.pone.0158691Jun Chen, Thomas Källman, Xiao-Fei Ma, Giusi Zaina, Michele Morgante, Martin Lascoux Identifying Genetic Signatures of Natural Selection Using Pooled Population Sequencing in Picea abies, G3 Genes|Genomes|Genetics 6, no.77 (Jul 2016): 1979–1989.https://doi.org/10.1534/g3.116.028753Jay F. Storz, Zachary A. Cheviron Functional Genomic Insights into Regulatory Mechanisms of High-Altitude Adaptation, (Jun 2016): 113–128.https://doi.org/10.1007/978-1-4899-7678-9_8Ryan J. Haasl, Bret A. Payseur Fifteen years of genomewide scans for selection: trends, lessons and unaddressed genetic sources of complication, Molecular Ecology 25, no.11 (Sep 2015): 5–23.https://doi.org/10.1111/mec.13339M. Szulkin, P.-A. Gagnaire, N. Bierne, A. Charmantier Population genomic footprints of fine-scale differentiation between habitats in Mediterranean blue tits, Molecular Ecology 25, no.22 (Jan 2016): 542–558.https://doi.org/10.1111/mec.13486H De Kort, K Vandepitte, J Mergeay, K V Mijnsbrugge, O Honnay The population genomic signature of environmental selection in the widespread insect-pollinated tree species Frangula alnus at different geographical scales, Heredity 115, no.55 (May 2015): 415–425.https://doi.org/10.1038/hdy.2015.41Sam Yeaman Local Adaptation by Alleles of Small Effect, The American Naturalist 186, no.S1S1 (Nov 2015): S74–S89.https://doi.org/10.1086/682405Archana Gauli, René E. Vaillancourt, Tanya G. Bailey, Dorothy A. Steane, Brad M. Potts Evidence for local climate adaptation in early-life traits of Tasmanian populations of Eucalyptus pauciflora, Tree Genetics & Genomes 11, no.55 (Sep 2015).https://doi.org/10.1007/s11295-015-0930-6Jay F. Storz, Jamie T. Bridgham, Scott A. Kelly, Theodore Garland Genetic approaches in comparative and evolutionary physiology, American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 309, no.33 (Aug 2015): R197–R214.https://doi.org/10.1152/ajpregu.00100.2015Juan P. Jaramillo-Correa, Julien Prunier, Alejandra Vázquez-Lobo, Stephen R. Keller, Alejandra Moreno-Letelier Molecular Signatures of Adaptation and Selection in Forest Trees, (Jan 2015): 265–306.https://doi.org/10.1016/bs.abr.2015.04.003L. Zhang, N. Huanqiong, Washington J. Gapare, S. K. Dillon, X. Li, H. X. Wu Comparison of allelic diversity between native gene resource plantings and selections in open-pollinated progeny test of Pinus radiata D. Don., Silvae Genetica 63, no.1-61-6 (Jun 2017): 213–221.https://doi.org/10.1515/sg-2014-0027Vincent Bourret, Mélanie Dionne, Louis Bernatchez Detecting genotypic changes associated with selective mortality at sea in Atlantic salmon: polygenic multilocus analysis surpasses genome scan, Molecular Ecology 23, no.1818 (Jun 2014): 4444–4457.https://doi.org/10.1111/mec.12798Jeremy J. Berg, Graham Coop, Marcus W. Feldman A Population Genetic Signal of Polygenic Adaptation, PLoS Genetics 10, no.88 (Aug 2014): e1004412.https://doi.org/10.1371/journal.pgen.1004412Outi 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/nrg3522Florian J. Alberto, Sally N. Aitken, Ricardo Alía, Santiago C. González‐Martínez, Heikki Hänninen, Antoine Kremer, François Lefèvre, Thomas Lenormand, Sam Yeaman, Ross Whetten, Outi Savolainen Potential for evolutionary responses to climate change – evidence from tree populations, Global Change Biology 19, no.66 (Apr 2013): 1645–1661.https://doi.org/10.1111/gcb.12181Carel P. van Schaik The costs and benefits of flexibility as an expression of behavioural plasticity: a primate perspective, Philosophical Transactions of the Royal Society B: Biological Sciences 368, no.16181618 (May 2013): 20120339.https://doi.org/10.1098/rstb.2012.0339M G Hamilton, D R Williams, P A Tilyard, E A Pinkard, T J Wardlaw, M Glen, R E Vaillancourt, B M Potts A latitudinal cline in disease resistance of a host tree, Heredity 110, no.44 (Dec 2012): 372–379.https://doi.org/10.1038/hdy.2012.106Asher D. Cutter, Richard Jovelin, Alivia Dey Molecular hyperdiversity and evolution in very large populations, Molecular Ecology 22, no.88 (Mar 2013): 2074–2095.https://doi.org/10.1111/mec.12281Julianne M. O’Reilly-Wapstra, Alison M. Miller, Matthew G. Hamilton, Dean Williams, Naomi Glancy-Dean, Brad M. Potts, Martin Heil Chemical Variation in a Dominant Tree Species: Population Divergence, Selection and Genetic Stability across Environments, PLoS ONE 8, no.33 (Mar 2013): e58416.https://doi.org/10.1371/journal.pone.0058416Tuomas Leinonen, R. J. Scott McCairns, Robert B. O'Hara, Juha Merilä QST–FST comparisons: evolutionary and ecological insights from genomic heterogeneity, Nature Reviews Genetics 14, no.33 (Feb 2013): 179–190.https://doi.org/10.1038/nrg3395Sonja T. Kujala, Outi Savolainen Sequence variation patterns along a latitudinal cline in Scots pine (Pinus sylvestris): signs of clinal adaptation?, Tree Genetics & Genomes 8, no.66 (Jun 2012): 1451–1467.https://doi.org/10.1007/s11295-012-0532-5Daniel K. Fabian, Martin Kapun, Viola Nolte, Robert Kofler, Paul S. Schmidt, Christian Schlötterer, Thomas Flatt Genome‐wide patterns of latitudinal differentiation among populations of D rosophila melanogaster from N orth A merica, Molecular Ecology 21, no.1919 (Aug 2012): 4748–4769.https://doi.org/10.1111/j.1365-294X.2012.05731.xJason A Holliday, Tongli Wang, Sally Aitken Predicting Adaptive Phenotypes From Multilocus Genotypes in Sitka Spruce ( Picea sitchensis ) Using Random Forest, G3 Genes|Genomes|Genetics 2, no.99 (Sep 2012): 1085–1093.https://doi.org/10.1534/g3.112.002733Jun Chen, Thomas Källman, Xiaofei Ma, Niclas Gyllenstrand, Giusi Zaina, Michele Morgante, Jean Bousquet, Andrew Eckert, Jill Wegrzyn, David Neale, Ulf Lagercrantz, Martin Lascoux Disentangling the Roles of History and Local Selection in Shaping Clinal Variation of Allele Frequencies and Gene Expression in Norway Spruce ( Picea abies ), Genetics 191, no.33 (Jul 2012): 865–881.https://doi.org/10.1534/genetics.112.140749BJÖRN ROGELL, JOHAN DANNEWITZ, STEFAN PALM, ERIK PETERSSON, JONAS DAHL, TORE PRESTEGAARD, TORBJÖRN JÄRVI, ANSSI LAURILA Strong divergence in trait means but not in plasticity across hatchery and wild populations of sea-run brown trout Salmo trutta, Molecular Ecology 21, no.1212 (Apr 2012): 2963–2976.https://doi.org/10.1111/j.1365-294X.2012.05590.xA Kremer, V Le Corre Decoupling of differentiation between traits and their underlying genes in response to divergent selection, Heredity 108, no.44 (Sep 2011): 375–385.https://doi.org/10.1038/hdy.2011.81VALÉRIE LE CORRE, ANTOINE KREMER The genetic differentiation at quantitative trait loci under local adaptation, Molecular Ecology 21, no.77 (Feb 2012): 1548–1566.https://doi.org/10.1111/j.1365-294X.2012.05479.xA.J. Lymbery, R.C.A. Thompson The molecular epidemiology of parasite infections: Tools and applications, Molecular and Biochemical Parasitology 181, no.22 (Feb 2012): 102–116.https://doi.org/10.1016/j.molbiopara.2011.10.006A C Brennan, D Barker, S J Hiscock, R J Abbott Molecular genetic and quantitative trait divergence associated with recent homoploid hybrid speciation: a study of Senecio squalidus (Asteraceae), Heredity 108, no.22 (Aug 2011): 87–95.https://doi.org/10.1038/hdy.2011.46Michael Krützen, Erik P. Willems, Carel P. van Schaik Culture and Geographic Variation in Orangutan Behavior, Current Biology 21, no.2121 (Nov 2011): 1808–1812.https://doi.org/10.1016/j.cub.2011.09.017B. RHONÉ, J.-T. BRANDENBURG, F. AUSTERLITZ Impact of selection on genes involved in regulatory network: a modelling study, Journal of Evolutionary Biology 24, no.1010 (Jun 2011): 2087–2098.https://doi.org/10.1111/j.1420-9101.2011.02335.xS. Volis Adaptive genetic differentiation in a predominantly self‐pollinating species analyzed by transplanting into natural environment, crossbreeding and QST – FST test, New Phytologist 192, no.11 (Jul 2011): 237–248.https://doi.org/10.1111/j.1469-8137.2011.03799.xDesmond J Stackpole, René E Vaillancourt, Ana Alves, José Rodrigues, Brad M Potts Genetic Variation in the Chemical Components of Eucalyptus globulus Wood, G3 Genes|Genomes|Genetics 1, no.22 (Jul 2011): 151–159.https://doi.org/10.1534/g3.111.000372 Sreejayan, U. Suresh Kumar, George Varghese, T. M. Jacob, George Thomas Stratification and population structure of the genetic resources of ancient medicinal rice (Oryza sativa L.) landrace Njavara, Genetic Resources and Crop Evolution 58, no.55 (Oct 2010): 697–711.https://doi.org/10.1007/s10722-010-9613-1Martin I. Lind, Pär K. Ingvarsson, Helena Johansson, David Hall, Frank Johansson GENE FLOW AND SELECTION ON PHENOTYPIC PLASTICITY IN AN ISLAND SYSTEM OF RANA TEMPORARIA, Evolution 65, no.33 (Oct 2010): 684–697.https://doi.org/10.1111/j.1558-5646.2010.01122.xAndrew P. Hendry, Michael T. Kinnison, Mikko Heino, Troy Day, Thomas B. Smith, Gary Fitt, Carl T. Bergstrom, John Oakeshott, Peter S. Jørgensen, Myron P. Zalucki, George Gilchrist, Simon Southerton, Andrew Sih, Sharon Strauss, Robert F. Denison, Scott P. Carroll Evolutionary principles and their practical application, Evolutionary Applications 4, no.22 (Feb 2011): 159–183.https://doi.org/10.1111/j.1752-4571.2010.00165.xM. G. Hamilton, P. A. Tilyard, D. R. Williams, R. E. Vaillancourt, T. J. Wardlaw, B. M. Potts The genetic variation in the timing of heteroblastic transition in Eucalyptus globulus is stable across environments, Australian Journal of Botany 59, no.22 (Jan 2011): 170.https://doi.org/10.1071/BT10313Xiao-Fei Ma, David Hall, Katherine R St Onge, Stefan Jansson, Pär K Ingvarsson Genetic Differentiation, Clinal Variation and Phenotypic Associations With Growth Cessation Across the Populus tremula Photoperiodic Pathway, Genetics 186, no.33 (Nov 2010): 1033–1044.https://doi.org/10.1534/genetics.110.120873J Derory, C Scotti-Saintagne, E Bertocchi, L Le Dantec, N Graignic, A Jauffres, M Casasoli, E Chancerel, C Bodenes, F Alberto, A Kremer Contrasting relations between diversity of candidate genes and variation of bud burst in natural and segregating populations of European oaks, Heredity 105, no.44 (Dec 2009): 401–411.https://doi.org/10.1038/hdy.2009.170Mathieu Siol, Stephen I. Wright, Spencer C. H. Barrett The population genomics of plant adaptation, New Phytologist 188, no.22 (Aug 2010): 313–332.https://doi.org/10.1111/j.1469-8137.2010.03401.xJay F. Storz, Christopher W. Wheat INTEGRATING EVOLUTIONARY AND FUNCTIONAL APPROACHES TO INFER ADAPTATION AT SPECIFIC LOCI, Evolution 64, no.99 (Sep 2010): 2489–2509.https://doi.org/10.1111/j.1558-5646.2010.01044.xAndrew J Eckert, Joost van Heerwaarden, Jill L Wegrzyn, C Dana Nelson, Jeffrey Ross-Ibarra, Santíago C González-Martínez, David B Neale Patterns of Population Structure and Environmental Associations to Aridity Across the Range of Loblolly Pine ( Pinus taeda L., Pinaceae), Genetics 185, no.33 (Jul 2010): 969–982.https://doi.org/10.1534/genetics.110.115543Antoine Kremer, Valérie Le Corre, Rémy J. Petit, Alexis Ducousso Historical and contemporary dynamics of adaptive differentiation in European oaks, (Jun 2010): 101–122.https://doi.org/10.1017/CBO9780511777592.006J Derory, C Scotti-Saintagne, E Bertocchi, L Le Dantec, N Graignic, A Jauffres, M Casasoli, E Chancerel, C Bodénès, F Alberto, A Kremer Contrasting relationships between the diversity of candidate genes and variation of bud burst in natural and segregating populations of European oaks, Heredity 104, no.55 (Oct 2009): 438–448.https://doi.org/10.1038/hdy.2009.134Bénédicte Rhoné, Renaud Vitalis, Isabelle Goldringer, Isabelle Bonnin EVOLUTION OF FLOWERING TIME IN EXPERIMENTAL WHEAT POPULATIONS: A COMPREHENSIVE APPROACH TO DETECT GENETIC SIGNATURES OF NATURAL SELECTION, Evolution 9 (Mar 2010).https://doi.org/10.1111/j.1558-5646.2010.00970.xANNA W. SANTURE, JOHN G. EWEN, DELPHINE SICARD, DEREK A. ROFF, ANDERS P. MØLLER Population structure in the barn swallow, Hirundo rustica: a comparison between neutral DNA markers and quantitative traits, Biological Journal of the Linnean Society 99, no.22 (Jan 2010): 306–314.https://doi.org/10.1111/j.1095-8312.2009.01366.xSoumaya Arraouadi, Mounawer Badri, Cheruth Abdul Jaleel, Naceur Djébali, Houcine Ilahi, Thierry Huguet, Mohamed Elarbi Aouani Analysis of Genetic Variation in Natural Populations of Medicago truncatula of Southern Tunisian Ecological Areas, Using Morphological Traits and SSR Markers, Tropical Plant Biology 2, no.3-43-4 (Sep 2009): 122–132.https://doi.org/10.1007/s12042-009-9034-5John Novembre, Anna Di Rienzo Spatial patterns of variation due to natural selection in humans, Nature Reviews Genetics 10, no.1111 (Oct 2009): 745–755.https://doi.org/10.1038/nrg2632Isabelle Olivieri Alternative mechanisms of range expansion are associated with different changes of evolutionary potential, Trends in Ecology & Evolution 24, no.66 (Jun 2009): 289–292.https://doi.org/10.1016/j.tree.2009.01.015Magdalena P. Bartkowska, Mark O. Johnston QUANTITATIVE GENETIC VARIATION IN POPULATIONS OF AMSINCKIA SPECTABILIS THAT DIFFER IN RATE OF SELF-FERTILIZATION, Evolution 63, no.55 (May 2009): 1103–1117.https://doi.org/10.1111/j.1558-5646.2008.00607.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.xWitold Wachowiak, Peter A. Balk, Outi Savolainen Search for nucleotide diversity patterns of local adaptation in dehydrins and other cold-related candidate genes in Scots pine (Pinus sylvestris L.), Tree Genetics & Genomes 5, no.11 (Nov 2008): 117–132.https://doi.org/10.1007/s11295-008-0188-3M.E. Horning, R.C. Cronn Development of variable microsatellite loci and range-wide characterization of nuclear genetic diversity in the important dryland shrub antelope bitterbrush (Purshia tridentata), Journal of Arid Environments 73, no.11 (Jan 2009): 7–13.https://doi.org/10.1016/j.jaridenv.2008.06.019Anna W Santure, Jinliang Wang The Joint Effects of Selection and Dominance on the Q ST − F ST Contrast, Genetics 181, no.11 (Jan 2009): 259–276.https://doi.org/10.1534/genetics.108.097998Mounawer Badri, Adel Zitoun, Houcine Ilahi, Thierry Huguet, Mohamed Elarbi Aouani Morphological and microsatellite diversity associated with ecological factors in natural populations of Medicago laciniata Mill. (Fabaceae), Journal of Genetics 87, no.33 (Nov 2008): 241–255.https://doi.org/10.1007/s12041-008-0038-yJudith R. Miller, Bryan P. Wood, Matthew B. Hamilton FST and QST Under Neutrality, Genetics 180, no.22 (Sep 2008): 1023–1037.https://doi.org/10.1534/genetics.108.092031MICHAEL C. WHITLOCK Evolutionary inference from QST, Molecular Ecology 17, no.88 (Mar 2008): 1885–1896.https://doi.org/10.1111/j.1365-294X.2008.03712.xPär K Ingvarsson, M Victoria Garcia, Virginia Luquez, David Hall, Stefan Jansson Nucleotide Polymorphism and Phenotypic Associations Within and Around the phytochrome B2 Locus in European Aspen ( Populus tremula , Salicaceae), Genetics 178, no.44 (Apr 2008): 2217–2226.https://doi.org/10.1534/genetics.107.082354T. LEINONEN, R. B. O’HARA, J. M. CANO, J. MERILÄ Comparative studies of quantitative trait and neutral marker divergence: a meta-analysis, Journal of Evolutionary Biology 21, no.11 (Nov 2007): 1–17.https://doi.org/10.1111/j.1420-9101.2007.01445.xDavid Hall, Virginia Luquez, Victoria M. Garcia, Kate R. St Onge, Stefan Jansson, Pär K. Ingvarsson ADAPTIVE POPULATION DIFFERENTIATION IN PHENOLOGY ACROSS A LATITUDINAL GRADIENT IN EUROPEAN ASPEN (POPULUS TREMULA, L.): A COMPARISON OF NEUTRAL MARKERS, CANDIDATE GENES AND PHENOTYPIC TRAITS, Evolution 61, no.1212 (Dec 2007): 2849–2860.https://doi.org/10.1111/j.1558-5646.2007.00230.xOuti Savolainen, Tanja Pyhäjärvi, Timo Knürr Gene Flow and Local Adaptation in Trees, Annual Review of Ecology, Evolution, and Systematics 38, no.11 (Dec 2007): 595–619.https://doi.org/10.1146/annurev.ecolsys.38.091206.095646ELODIE CHAPUIS, SANDRINE TROUVE, BENOIT FACON, LOÏC DEGEN, JEROME GOUDET High quantitative and no molecular differentiation of a freshwater snail (Galba truncatula) between temporary and permanent water habitats, Molecular Ecology 16, no.1616 (Aug 2007): 3484–3496.https://doi.org/10.1111/j.1365-294X.2007.03386.xM. I. LIND, F. JOHANSSON The degree of adaptive phenotypic plasticity is correlated with the spatial environmental heterogeneity experienced by island populations of Rana temporaria, Journal of Evolutionary Biology 20, no.44 (Jul 2007): 1288–1297.https://doi.org/10.1111/j.1420-9101.2007.01353.xJ. M. CANO, C. MATSUBA, H. MÄKINEN, J. MERILÄ The utility of QTL-Linked markers to detect selective sweeps in natural populations - a case study of the EDA gene and a linked marker in threespine stickleback, Molecular Ecology 15, no.1414 (Nov 2006): 4613–4621.https://doi.org/10.1111/j.1365-294X.2006.03099.xMAXIME PAUWELS, HÉLÈNE FRÉROT, ISABELLE BONNIN, PIERRE SAUMITOU-LAPRADE A broad-scale analysis of population differentiation for Zn tolerance in an emerging model species for tolerance study: Arabidopsis halleri (Brassicaceae), Journal of Evolutionary Biology 19, no.66 (Nov 2006): 1838–1850.https://doi.org/10.1111/j.1420-9101.2006.01178.xDorothy A. Steane, Natalie Conod, Rebecca C. Jones, René E. Vaillancourt, Bradley M. Potts A comparative analysis of population structure of a forest tree, Eucalyptus globulus (Myrtaceae), using microsatellite markers and quantitative traits, Tree Genetics & Genomes 2, no.11 (Jan 2006): 30–38.https://doi.org/10.1007/s11295-005-0028-7M. TAPIO, I. TAPIO, Z. GRISLIS, L.-E. HOLM, S. JEPPSSON, J. KANTANEN, I. MICEIKIENE, I. OLSAKER, H. VIINALASS, E. EYTHORSDOTTIR Native breeds demonstrate high contributions to the molecular variation in northern European sheep, Molecular Ecology 14, no.1313 (Oct 2005): 3951–3963.https://doi.org/10.1111/j.1365-294X.2005.02727.xM.A Toro, A Caballero Characterization and conservation of genetic diversity in subdivided populations, Philosophical Transactions of the Royal Society B: Biological Sciences 360, no.14591459 (Jul 2005): 1367–1378.https://doi.org/10.1098/rstb.2005.1680H. SANOU, P. N. LOVETT, J.-M. BOUVET Comparison of quantitative and molecular variation in agroforestry populations of the shea tree (Vitellaria paradoxa C.F. Gaertn) in Mali, Molecular Ecology 14, no.88 (Jul 2005): 2601–2610.https://doi.org/10.1111/j.1365-294X.2005.02601.xP Waldmann, M R García-Gil, M J Sillanpää Comparing Bayesian estimates of genetic differentiation of molecular markers and quantitative traits: an application to Pinus sylvestris, Heredity 94, no.66 (Apr 2005): 623–629.https://doi.org/10.1038/sj.hdy.6800672T J Morgan, M A Evans, T Garland, J G Swallow, P A Carter Molecular and quantitative genetic divergence among populations of house mice with known evolutionary histories, Heredity 94, no.55 (Mar 2005): 518–525.https://doi.org/10.1038/sj.hdy.6800652JAY F. STORZ INVITED REVIEW: Using genome scans of DNA polymorphism to infer adaptive population divergence, Molecular Ecology 14, no.33 (Jan 2005): 671–688.https://doi.org/10.1111/j.1365-294X.2005.02437.xS. M. ROGERS, L. BERNATCHEZ FAST-TRACK: Integrating QTL mapping and genome scans towards the characterization of candidate loci under parallel selection in the lake whitefish (Coregonus clupeaformis), Molecular Ecology 14, no.22 (Dec 2004): 351–361.https://doi.org/10.1111/j.1365-294X.2004.02396.xKelly Gravuer, Eric von Wettberg, Johanna Schmitt , Biological Conservation 124, no.22 ( 2005): 155.https://doi.org/10.1016/j.biocon.2005.01.021Robert G Latta Relating processes to patterns of genetic variation across landscapes, Forest Ecology and Management 197, no.1-31-3 (Aug 2004): 91–102.https://doi.org/10.1016/j.foreco.2004.05.007François Lefèvre Human impacts on forest genetic resources in the temperate zone: an updated review, Forest Ecology and Management 197, no.1-31-3 (Aug 2004): 257–271.https://doi.org/10.1016/j.foreco.2004.05.017David B Neale, Outi Savolainen Association genetics of complex traits in conifers, Trends in Plant Science 9, no.77 (Jul 2004): 325–330.https://doi.org/10.1016/j.tplants.2004.05.006Emmanuelle Porcher, Tatiana Giraud, Isabelle Goldringer, Claire Lavigne EXPERIMENTAL DEMONSTRATION OF A CAUSAL RELATIONSHIP BETWEEN HETEROGENEITY OF SELECTION AND GENETIC DIFFERENTIATION IN QUANTITATIVE TRAITS, Evolution 58, no.77 (Jul 2004): 1434–1445.https://doi.org/10.1111/j.0014-3820.2004.tb01725.xRobert G. Latta Gene flow, adaptive population divergence and comparative population structure across loci, New Phytologist 161, no.11 (Dec 2003): 51–58.https://doi.org/10.1046/j.1469-8137.2003.00920.xValérie Le Corre, Antoine Kremer Genetic Variability at Neutral Markers, Quantitative Trait Loci and Trait in a Subdivided Population Under Selection, Genetics 164, no.33 (Jul 2003): 1205–1219.https://doi.org/10.1093/genetics/164.3.1205M. R. García‐Gil, M. Mikkonen, O. Savolainen Nucleotide diversity at two phytochrome loci along a latitudinal cline in Pinus sylvestris, Molecular Ecology 12, no.55 (Apr 2003): 1195–1206.https://doi.org/10.1046/j.1365-294X.2003.01826.xJay F. Storz Contrasting patterns of divergence in quantitative traits and neutral DNA markers: analysis of clinal variation, Molecular Ecology 11, no.1212 (Oct 2008): 2537–2551.https://doi.org/10.1046/j.1365-294X.2002.01636.xT. Steinger, P. Haldimann, K. A. Leiss, H. Müller-Schärer Does natural selection promote population divergence? A comparative analysis of population structure using amplified fragment length polymorphism markers and quantitative traits, Molecular Ecology 11, no.1212 (Oct 2008): 2583–2590.https://doi.org/10.1046/j.1365-294X.2002.01653.xRobert G Latta, John K McKay Genetic population divergence: markers and traits, Trends in Ecology & Evolution 17, no.1111 (Nov 2002): 501–502.https://doi.org/10.1016/S0169-5347(02)02601-0John K. McKay, Robert G. Latta Adaptive population divergence: markers, QTL and traits, Trends in Ecology & Evolution 17, no.66 (Jun 2002): 285–291.https://doi.org/10.1016/S0169-5347(02)02478-3Marita Kruskopf Österberg, Oksana Shavorskaya, Martin Lascoux, Ulf Lagercrantz Naturally Occurring Indel Variation in the Brassica nigra COL1 Gene Is Associated With Variation in Flowering Time, Genetics 161, no.11 (May 2002): 299–306.https://doi.org/10.1093/genetics/161.1.299C. C. Mundt, L. P. Nieva, C. M. Vera Cruz Variation for aggressiveness within and between lineages of Xanthomonas oryzae pv. oryzae, Plant Pathology 51, no.22 (Nov 2002): 163–168.https://doi.org/10.1046/j.1365-3059.2002.00674.xKimmo Rumpunen, Igor V. Bartish Comparison of differentiation estimates based on morphometric and molecular data, exemplified by various leaf shape descriptors and RAPDs in the genus Chaenomeles (Rosaceae), TAXON 51, no.11 (Feb 2002): 69–82.https://doi.org/10.2307/1554964J. Merilä, P. Crnokrak Comparison of genetic differentiation at marker loci and quantitative traits, Journal of Evolutionary Biology 14, no.66 (Dec 2001): 892–903.https://doi.org/10.1046/j.1420-9101.2001.00348.xChristophe Petit, Hélène Fréville, Agnès Mignot, Bruno Colas, Miquel Riba, Eric Imbert, Sylvie Hurtrez-Boussés, Myriam Virevaire, Isabelle Olivieri Gene flow and local adaptation in two endemic plant species, Biological Conservation 100, no.11 (Jul 2001): 21–34.https://doi.org/10.1016/S0006-3207(00)00204-4Wendy K. Gram, Victoria L. Sork ASSOCIATION BETWEEN ENVIRONMENTAL AND GENETIC HETEROGENEITY IN FOREST TREE POPULATIONS, Ecology 82, no.77 (Jul 2001): 2012–2021.https://doi.org/10.1890/0012-9658(2001)082[2012:ABEAGH]2.0.CO;2 Waldmann, Andersson Comparison of genetic (co)variance matrices within and between Scabiosa canescens and S. columbaria, Journal of Evolutionary Biology 13, no.55 (Oct 2000): 826–835.https://doi.org/10.1046/j.1420-9101.2000.00214.xKermit Ritland Marker-inferred relatedness as a tool for detecting heritability in nature, Molecular Ecology 9, no.99 (Sep 2000): 1195–1204.https://doi.org/10.1046/j.1365-294x.2000.00971.xR G. Doupé, A J. Lymbery Managing translocations of aquatic species, Aquaculture Research 31, no.11 (Dec 2001): 151–156.https://doi.org/10.1046/j.1365-2109.2000.00434.xPatrik Waldmann, Stefan Andersson Multilocus and Multitrait Differentiation of Populations of the Locally Rare Plant Scabiosa Canescens and the more Common S. Columbaria, Hereditas 130, no.33 (May 2004): 341–343.https://doi.org/10.1111/j.1601-5223.1999.00341.x
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