FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2047441390> ?p ?o ?g. }

• W2047441390 endingPage "145" @default.
• W2047441390 startingPage "141" @default.
• W2047441390 abstract "Previous articleNext article No AccessNotes and CommentsThe Genetic Basis of Species Differences in PlantsJerry A. Coyne, and Russell LandeJerry A. Coyne Search for more articles by this author , and Russell Lande Search for more articles by this author PDFPDF PLUS Add to favoritesDownload CitationTrack CitationsPermissionsReprints Share onFacebookTwitterLinkedInRedditEmail SectionsMoreDetailsFiguresReferencesCited by The American Naturalist Volume 126, Number 1Jul., 1985 Published for The American Society of Naturalists Article DOIhttps://doi.org/10.1086/284404 Views: 13Total views on this site Citations: 58Citations are reported from Crossref Copyright 1985 The University of ChicagoPDF download Crossref reports the following articles citing this article:Alan Álvarez-Holguín, Carlos Raúl Morales-Nieto, Raúl Corrales-Lerma, Jesús Alejandro Prieto-Amparán, Federico Villarreal-Guerrero, Ricardo Alonso Sánchez-Gutiérrez, Craig Eliot Coleman Genetic structure and temporal environmental niche dynamics of sideoats grama [Bouteloua curtipendula (Michx.) Torr.] populations in Mexico, PLOS ONE 16, no.77 (Jul 2021): e0254566.https://doi.org/10.1371/journal.pone.0254566Balsam Al-Janabi, Martin Wahl, Ulf Karsten, Angelika Graiff, Inken Kruse Sensitivities to global change drivers may correlate positively or negatively in a foundational marine macroalga, Scientific Reports 9, no.11 (Oct 2019).https://doi.org/10.1038/s41598-019-51099-8Stefan Andersson Ecotypic divergence in Crepis tectorum (Asteraceae): inferring trait lability and correlational constraints from hormonally manipulated phenotypes, Nordic Journal of Botany 37, no.33 (Mar 2019).https://doi.org/10.1111/njb.02236Katrina L. Tso, Gerard J. Allan Environmental variation shapes genetic variation in Bouteloua gracilis : Implications for restoration management of natural populations and cultivated varieties in the southwestern United States, Ecology and Evolution 9, no.11 (Dec 2018): 482–499.https://doi.org/10.1002/ece3.4767Alexander Gamisch, Gunter Alexander Fischer, Hans Peter Comes Multiple independent origins of auto-pollination in tropical orchids (Bulbophyllum) in light of the hypothesis of selfing as an evolutionary dead end, BMC Evolutionary Biology 15, no.11 (Sep 2015).https://doi.org/10.1186/s12862-015-0471-5Troy E. Wood, Kyle Doherty, Wayne Padgett Development of Native Plant Materials for Restoration and Rehabilitation of Colorado Plateau Ecosystems, Natural Areas Journal 35, no.11 (Jan 2015): 134–150.https://doi.org/10.3375/043.035.0117Alexander Gamisch, Gunter A. Fischer, Hans Peter Comes Recurrent polymorphic mating type variation in Madagascan Bulbophyllum species (Orchidaceae) exemplifies a high incidence of auto-pollination in tropical orchids, Botanical Journal of the Linnean Society 175, no.22 (May 2014): 242–258.https://doi.org/10.1111/boj.12168Jennifer M. Sunday, Piero Calosi, Sam Dupont, Philip L. Munday, Jonathon H. Stillman, Thorsten B.H. Reusch Evolution in an acidifying ocean, Trends in Ecology & Evolution 29, no.22 (Feb 2014): 117–125.https://doi.org/10.1016/j.tree.2013.11.001Hans Peter Comes Konrad Bachmann (1939-2012), TAXON 62, no.11 (Feb 2013): 193–196.https://doi.org/10.1002/tax.621030Joëlle Ronfort, Sylvain Glemin MATING SYSTEM, HALDANE'S SIEVE, AND THE DOMESTICATION PROCESS, Evolution (Dec 2012): no–no.https://doi.org/10.1111/evo.12025Alison Scoville, Young Wha Lee, John H. Willis, John K. Kelly Contribution of chromosomal polymorphisms to the G‐matrix of Mimulus guttatus, New Phytologist 183, no.33 (Jul 2009): 803–815.https://doi.org/10.1111/j.1469-8137.2009.02947.xTHORSTEN B. H. REUSCH, TROY E. WOOD Molecular ecology of global change, Molecular Ecology 16, no.1919 (Aug 2007): 3973–3992.https://doi.org/10.1111/j.1365-294X.2007.03454.xJeffrey Ross-Ibarra, Peter L. Morrell, Brandon S. Gaut Plant domestication, a unique opportunity to identify the genetic basis of adaptation, Proceedings of the National Academy of Sciences 104, no.suppl_1suppl_1 (May 2007): 8641–8648.https://doi.org/10.1073/pnas.0700643104Megan C Hall, Christopher J Basten, John H Willis Pleiotropic Quantitative Trait Loci Contribute to Population Divergence in Traits Associated With Life-History Variation in Mimulus guttatus, Genetics 172, no.33 (Mar 2006): 1829–1844.https://doi.org/10.1534/genetics.105.051227Troy E. Wood, John M. Burke, Loren H. Rieseberg Parallel genotypic adaptation: when evolution repeats itself, Genetica 123, no.1-21-2 (Feb 2005): 157–170.https://doi.org/10.1007/s10709-003-2738-9O. Gailing, M. R. Macnair, K. Bachmann QTL Mapping for a Trade‐Off between Leaf and Bud Production in a Recombinant Inbred Population of Microseris douglasii and M. bigelovii (Asteraceae, Lactuceae): A Potential Preadaptation for the Colonization of Serpentine Soils, Plant Biology 6, no.44 (Jun 2008): 440–446.https://doi.org/10.1055/s-2004-817958Lila Fishman, Donald A. Stratton THE GENETICS OF FLORAL DIVERGENCE AND POSTZYGOTIC BARRIERS BETWEEN OUTCROSSING AND SELFING POPULATIONS OF ARENARIA UNIFLORA (CARYOPHYLLACEAE), Evolution 58, no.22 (May 2007): 296–307.https://doi.org/10.1111/j.0014-3820.2004.tb01646.xO. Gailing, K. Bachmann QTL mapping reveals a two-step model for the evolutionary reduction of inner microsporangia within the asteracean genus Microseris, Theoretical and Applied Genetics 107, no.55 (Jul 2003): 893–901.https://doi.org/10.1007/s00122-003-1324-y David L. Remington and Michael D. Purugganan Candidate Genes, Quantitative Trait Loci, and Functional Trait Evolution in Plants Remington & Purugganan, International Journal of Plant Sciences 164, no.S3S3 (Jul 2015): S7–S20.https://doi.org/10.1086/367812Miltos Tsiantis, Angela Hay Comparative plant development: the time of the leaf?, Nature Reviews Genetics 4, no.33 (Mar 2003): 169–180.https://doi.org/10.1038/nrg1002L. H. Rieseberg, J. M. Burke A genic view of species integration, Journal of Evolutionary Biology 14, no.66 (Dec 2001): 883–886.https://doi.org/10.1046/j.1420-9101.2001.00339.xD. M. L. Moritz, J. W. Kadereit The Genetics of Evolutionary Change in Senecio vulgaris L.: A QTL Mapping Approach, Plant Biology 3, no.55 (Sep 2001): 544–552.https://doi.org/10.1055/s-2001-17733Rodney Mauricio Mapping quantitative trait loci in plants: uses and caveats for evolutionary biology, Nature Reviews Genetics 2, no.55 (May 2001): 370–381.https://doi.org/10.1038/35072085Laura F. Galloway, Charles B. Fenster NUCLEAR AND CYTOPLASMIC CONTRIBUTIONS TO INTRASPECIFIC DIVERGENCE IN AN ANNUAL LEGUME, Evolution 55, no.33 (May 2007): 488–497.https://doi.org/10.1111/j.0014-3820.2001.tb00783.xSpencer C. H. Barrett THE LIFE AND TIMES OF PLANT SPECIES: FROM METAPOPULATIONS TO MUTATIONAL MELTDOWN1, Evolution 55, no.33 (May 2007): 641–646.https://doi.org/10.1111/j.0014-3820.2001.tb00798.xKonrad Bachmann Evolution and the genetic analysis of populations: 1950–2000, TAXON 50, no.11 (Feb 2001): 7–45.https://doi.org/10.2307/1224510Donald A. Levin 50 years of plant speciation, TAXON 50, no.11 (Feb 2001): 69–91.https://doi.org/10.2307/1224512Laura F. Galloway, Charles B. Fenster , Evolution 55, no.33 ( 2001): 488.https://doi.org/10.1554/0014-3820(2001)055[0488:NACCTI]2.0.CO;2Spencer C. H. Barrett , Evolution 55, no.33 ( 2001): 641.https://doi.org/10.1554/0014-3820(2001)055[0641:TLATOP]2.0.CO;2Robert Bleiweiss MIMICRY ON THE QT(L): GENETICS OF SPECIATION IN MIMULUS, Evolution 55, no.88 (Jan 2001): 1706.https://doi.org/10.1554/0014-3820(2001)055[1706:MOTQLG]2.0.CO;2Michael D. Purugganan The molecular population genetics of regulatory genes, Molecular Ecology 9, no.1010 (Oct 2000): 1451–1461.https://doi.org/10.1046/j.1365-294x.2000.01016.xJing-Zhong Lin The relationship between loci for mating system and fitness-related traits in Mimulus (Scrophulariaceae): A test for deleterious pleiotropy of QTLs with large effects, Genome 43, no.44 (Aug 2000): 628–633.https://doi.org/10.1139/g00-032David L. Stern PERSPECTIVE: EVOLUTIONARY DEVELOPMENTAL BIOLOGY AND THE PROBLEM OF VARIATION, Evolution 54, no.44 (Jan 2000): 1079.https://doi.org/10.1554/0014-3820(2000)054[1079:PEDBAT]2.0.CO;2Douglas W. Schemske, H. D. Bradshaw Pollinator preference and the evolution of floral traits in monkeyflowers ( Mimulus ), Proceedings of the National Academy of Sciences 96, no.2121 (Oct 1999): 11910–11915.https://doi.org/10.1073/pnas.96.21.11910Hiroyuki Shibaike Molecular genetic mapping and plant evolutionary biology, Journal of Plant Research 111, no.33 (Sep 1998): 383–388.https://doi.org/10.1007/BF02507802H D Bradshaw, Kevin G Otto, Barbara E Frewen, John K McKay, Douglas W Schemske Quantitative Trait Loci Affecting Differences in Floral Morphology Between Two Species of Monkeyflower (Mimulus), Genetics 149, no.11 (May 1998): 367–382.https://doi.org/10.1093/genetics/149.1.367Eric Routman, James M. Cheverud Quantitative trait loci: a new approach to old evolutionary problems, (Jan 1998): 211–220.https://doi.org/10.1007/978-3-0348-8948-3_11H. Allen Orr, Shannon Irving THE GENETICS OF ADAPTATION: THE GENETIC BASIS OF RESISTANCE TO WASP PARASITISM IN DROSOPHILA MELANOGASTER, Evolution 51, no.66 (May 2017): 1877–1885.https://doi.org/10.1111/j.1558-5646.1997.tb05110.xJohn R. True, Jianjun Liu, Lynn F. Stam, Zhao-Bang Zeng, Cathy C. Laurie QUANTITATIVE GENETIC ANALYSIS OF DIVERGENCE IN MALE SECONDARY SEXUAL TRAITS BETWEEN DROSOPHILA SIMULANS AND DROSOPHILA MAURITIANA, Evolution 51, no.33 (May 2017): 816–832.https://doi.org/10.1111/j.1558-5646.1997.tb03664.xCharles B Fenster, Pamela K Diggle, Spencer C H Barrett, Kermit Ritland The genetics of floral development differentiating two species of Mimulus (Scrophulariaceae), Heredity 74, no.33 (Mar 1995): 258–266.https://doi.org/10.1038/hdy.1995.39R. Wu, R. F. Stettler Quantitative genetics of growth and development in Populus. I. A three-generation comparison of tree architecture during the first 2 years of growth, Theoretical and Applied Genetics 89-89, no.7-87-8 (Dec 1994): 1046–1054.https://doi.org/10.1007/BF00224537Charles B Fenster, Kermit Ritland Quantitative genetics of mating system divergence in the yellow monkeyflower species complex, Heredity 73, no.44 (Oct 1994): 422–435.https://doi.org/10.1038/hdy.1994.190Charles B Fenster, Spencer C H Barrett Inheritance of mating-system modifier genes in Eichhornia paniculata (Pontederiaceae), Heredity 72, no.55 (May 1994): 433–445.https://doi.org/10.1038/hdy.1994.62Wim van Houten, Leo van Raamsdonk, Konrad Bachmann Intraspecific evolution ofMicroseris pygmaea (Asteraceae, Lactuceae) analyzed by cosegregation of phenotypic characters (QTLs) and molecular markers (RAPDs), Plant Systematics and Evolution 190, no.1-21-2 (Mar 1994): 49–67.https://doi.org/10.1007/BF00937858Richard Whitkus, John Doebley, Jonathan F. Wendel Nuclear DNA markers in systematics and evolution, (Jan 1994): 116–141.https://doi.org/10.1007/978-94-011-1104-1_6Jeffrey Conner Tests for major genes affecting quantitative traits in wild radish,Raphanus raphanistrum, Genetica 90, no.11 (Feb 1993): 41–45.https://doi.org/10.1007/BF01435177Paul Gepts The Use of Molecular and Biochemical Markers in Crop Evolution Studies, (Jan 1993): 51–94.https://doi.org/10.1007/978-1-4615-2878-4_3R. F. Stettler, R. J. Ceulemans Clonal Material as a Focus for Genetic and Physiological Research in Forest Trees, (Jan 1993): 68–86.https://doi.org/10.1007/978-3-642-84175-0_6 Loren H. Rieseberg The Genetic Basis of Morphological Differences between Plant Species, International Journal of Plant Sciences 153, no.11 (Oct 2015): v–vi.https://doi.org/10.1086/ijps.153.1.2995698S. C. H. Barrett Heterostylous Genetic Polymorphisms: Model Systems for Evolutionary Analysis, (Jan 1992): 1–29.https://doi.org/10.1007/978-3-642-86656-2_1Mark R. Macnair Genetics of the Resistance of Plants to Pollutants, (Jan 1991): 127–136.https://doi.org/10.1007/978-1-4612-3060-1_7M. R. Macnair Why the evolution of resistance to anthropogenic toxins normally involves major gene changes: the limits to natural selection, Genetica 84, no.33 (Jan 1991): 213–219.https://doi.org/10.1007/BF00127250D. H. Benzing The Evolution of Epiphytism, (Jan 1989): 15–41.https://doi.org/10.1007/978-3-642-74465-5_2Edward O. Guerrant Heterochrony in Plants, (Jan 1988): 111–133.https://doi.org/10.1007/978-1-4899-0795-0_7Benton M. Stidd Telomes, theory change, and the evolution of vascular plants, Review of Palaeobotany and Palynology 50, no.1-21-2 (Feb 1987): 115–126.https://doi.org/10.1016/0034-6667(87)90042-XP. A. Parsons Evolutionary Rates under Environmental Stress, (Jan 1987): 311–347.https://doi.org/10.1007/978-1-4615-6986-2_10 L. D. Gottlieb Reply to Coyne and Lande, The American Naturalist 126, no.11 (Oct 2015): 146–150.https://doi.org/10.1086/284405Troy E. Wood, John M. Burke, Loren H. Rieseberg Parallel genotypic adaptation: when evolution repeats itself, (): 157–170.https://doi.org/10.1007/1-4020-3836-4_14" @default.
• W2047441390 created "2016-06-24" @default.
• W2047441390 creator A5049319800 @default.
• W2047441390 creator A5072074495 @default.
• W2047441390 date "1985-07-01" @default.
• W2047441390 modified "2023-10-16" @default.
• W2047441390 title "The Genetic Basis of Species Differences in Plants" @default.
• W2047441390 cites W1042208802 @default.
• W2047441390 cites W1774723416 @default.
• W2047441390 cites W1891728252 @default.
• W2047441390 cites W1944048986 @default.
• W2047441390 cites W1980592356 @default.
• W2047441390 cites W2020524544 @default.
• W2047441390 cites W2095098262 @default.
• W2047441390 cites W2253707868 @default.
• W2047441390 cites W288427366 @default.
• W2047441390 cites W3146647032 @default.
• W2047441390 cites W3184991942 @default.
• W2047441390 doi "https://doi.org/10.1086/284404" @default.
• W2047441390 hasPublicationYear "1985" @default.
• W2047441390 type Work @default.
• W2047441390 sameAs 2047441390 @default.
• W2047441390 citedByCount "71" @default.
• W2047441390 countsByYear W20474413902012 @default.
• W2047441390 countsByYear W20474413902013 @default.
• W2047441390 countsByYear W20474413902014 @default.
• W2047441390 countsByYear W20474413902015 @default.
• W2047441390 countsByYear W20474413902018 @default.
• W2047441390 countsByYear W20474413902019 @default.
• W2047441390 countsByYear W20474413902021 @default.
• W2047441390 crossrefType "journal-article" @default.
• W2047441390 hasAuthorship W2047441390A5049319800 @default.
• W2047441390 hasAuthorship W2047441390A5072074495 @default.
• W2047441390 hasConcept C12426560 @default.
• W2047441390 hasConcept C18903297 @default.
• W2047441390 hasConcept C2524010 @default.
• W2047441390 hasConcept C33923547 @default.
• W2047441390 hasConcept C78458016 @default.
• W2047441390 hasConcept C86803240 @default.
• W2047441390 hasConceptScore W2047441390C12426560 @default.
• W2047441390 hasConceptScore W2047441390C18903297 @default.
• W2047441390 hasConceptScore W2047441390C2524010 @default.
• W2047441390 hasConceptScore W2047441390C33923547 @default.
• W2047441390 hasConceptScore W2047441390C78458016 @default.
• W2047441390 hasConceptScore W2047441390C86803240 @default.
• W2047441390 hasIssue "1" @default.
• W2047441390 hasLocation W20474413901 @default.
• W2047441390 hasOpenAccess W2047441390 @default.
• W2047441390 hasPrimaryLocation W20474413901 @default.
• W2047441390 hasRelatedWork W1997770566 @default.
• W2047441390 hasRelatedWork W2006264290 @default.
• W2047441390 hasRelatedWork W2034736453 @default.
• W2047441390 hasRelatedWork W2055925137 @default.
• W2047441390 hasRelatedWork W2061542922 @default.
• W2047441390 hasRelatedWork W2422215742 @default.
• W2047441390 hasRelatedWork W4235748225 @default.
• W2047441390 hasRelatedWork W4236969087 @default.
• W2047441390 hasRelatedWork W4250751887 @default.
• W2047441390 hasRelatedWork W4250812939 @default.
• W2047441390 hasVolume "126" @default.
• W2047441390 isParatext "false" @default.
• W2047441390 isRetracted "false" @default.
• W2047441390 magId "2047441390" @default.
• W2047441390 workType "article" @default.