The Significance of Polyploidy in Plant Evolution
1940; University of Chicago Press; Volume: 74; Issue: 750 Linguagem: Inglês
10.1086/280872
ISSN1537-5323
Autores Tópico(s)Chromosomal and Genetic Variations
ResumoPrevious articleNext article No AccessThe Significance of Polyploidy in Plant EvolutionG. Ledyard Stebbins, Jr.G. Ledyard Stebbins, Jr.PDFPDF PLUS Add to favoritesDownload CitationTrack CitationsPermissionsReprints Share onFacebookTwitterLinkedInRedditEmailPrint SectionsMoreDetailsFiguresReferencesCited by The American Naturalist Volume 74, Number 750Jan. - Feb., 1940 Published for The American Society of Naturalists Article DOIhttps://doi.org/10.1086/280872 Views: 146Total views on this site Citations: 111Citations are reported from Crossref PDF download Crossref reports the following articles citing this article:Hyoung Tae Kim, Sang Hee Park, Jung Sung Kim Dynamic hybridization between two spleenworts, Asplenium incisum and Asplenium ruprechtii in Korea, Frontiers in Plant Science 14 (Jul 2023).https://doi.org/10.3389/fpls.2023.1116040William A. Freyman, Matthew G. Johnson, Carl J. 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The evolutionary impact of whole‐genome duplication on immunogenetic diversity and parasite load, Ecology and Evolution 10, no.2424 (Nov 2020): 13949–13956.https://doi.org/10.1002/ece3.6987Stacy A. Jorgensen, David S. Barrington Speciation and Reticulation in the Polystichum Allotetraploids of the Costa Rican Cordillera Talamanca, American Fern Journal 110, no.44 (Oct 2020).https://doi.org/10.1640/0002-8444-110.4.151David S. Barrington The Biogeography of Polyploid Ferns Across Space and Time, American Fern Journal 110, no.44 (Oct 2020).https://doi.org/10.1640/0002-8444-110.4.233Gonzalo Nieto Feliner, Josep Casacuberta, Jonathan F. Wendel Genomics of Evolutionary Novelty in Hybrids and Polyploids, Frontiers in Genetics 11 (Jul 2020).https://doi.org/10.3389/fgene.2020.00792Nathalie Gontier Testing the “(Neo-)Darwinian” Principles against Reticulate Evolution: How Variation, Adaptation, Heredity and Fitness, Constraints and Affordances, Speciation, and Extinction Surpass Organisms and Species, Information 11, no.77 (Jul 2020): 352.https://doi.org/10.3390/info11070352Juliana M. L. Lopes, Humberto Henrique Carvalho, Cristiane Zorzatto, Ana Luisa S. Azevedo, Marco Antonio Machado, Fátima Regina G. Salimena, Richard M. Grazul, Matthew A. Gitzendanner, Douglas E. Soltis, Pamela S. Soltis, Lyderson F. Viccini Genetic relationships and polyploid origins in the Lippia alba complex, American Journal of Botany 107, no.33 (Mar 2020): 466–476.https://doi.org/10.1002/ajb2.1443Adam B. Roddy, Guillaume Théroux-Rancourt, Tito Abbo, Joseph W. Benedetti, Craig R. Brodersen, Mariana Castro, Silvia Castro, Austin B. Gilbride, Brook Jensen, Guo-Feng Jiang, John A. Perkins, Sally D. Perkins, João Loureiro, Zuhah Syed, R. Alexander Thompson, Sara E. Kuebbing, and Kevin A. Simonin The Scaling of Genome Size and Cell Size Limits Maximum Rates of Photosynthesis with Implications for Ecological Strategies, International Journal of Plant Sciences 181, no.11 (Nov 2019): 75–87.https://doi.org/10.1086/706186D. Blaine Marchant, Emily B. Sessa, Paul G. Wolf, Kweon Heo, W. Brad Barbazuk, Pamela S. Soltis, Douglas E. Soltis The C-Fern (Ceratopteris richardii) genome: insights into plant genome evolution with the first partial homosporous fern genome assembly, Scientific Reports 9, no.11 (Dec 2019).https://doi.org/10.1038/s41598-019-53968-8, M. M. Ferrer, , M. d.R. Ruenes-Morales, , P.I. Montañez-Escalante, , J.G. Rivero-Manzanilla, Variation of chromosomal complement in the Mexican plum Spondias purpurea L.: polyploid series in landraces cultivated by Mayan of Yucatan, Fruits 74, no.44 (Aug 2019): 145–149.https://doi.org/10.17660/th2019/74.4.1Morgan W. Southgate, Nikisha R. Patel, David S. Barrington ECOLOGICAL OUTCOME OF ALLOPOLYPLOIDY IN ADIANTUM (PTERIDACEAE): NICHE INTERMEDIACY AND EXPANSION INTO NOVEL HABITATS, Rhodora 121, no.986986 (Apr 2019): 108.https://doi.org/10.3119/18-09Guanjing Hu, Jonathan F. Wendel Cis – trans controls and regulatory novelty accompanying allopolyploidization, New Phytologist 221, no.44 (Nov 2018): 1691–1700.https://doi.org/10.1111/nph.15515Hao Li, Chien-Hsun Huang, Hong Ma Whole-Genome Duplications in Pear and Apple, (Jul 2019): 279–299.https://doi.org/10.1007/978-3-030-11048-2_15Emily B. Sessa Polyploidy as a mechanism for surviving global change, New Phytologist 221, no.11 (Nov 2018): 5–6.https://doi.org/10.1111/nph.15513Marta Avramova, Alice Cibrario, Emilien Peltier, Monika Coton, Emmanuel Coton, Joseph Schacherer, Giuseppe Spano, Vittorio Capozzi, Giuseppe Blaiotta, Franck Salin, Marguerite Dols-Lafargue, Paul Grbin, Chris Curtin, Warren Albertin, Isabelle Masneuf-Pomarede Brettanomyces bruxellensis population survey reveals a diploid-triploid complex structured according to substrate of isolation and geographical distribution, Scientific Reports 8, no.11 (Mar 2018).https://doi.org/10.1038/s41598-018-22580-7David Kopecký, Tamina Felder, Franz X. Schubiger, Václav Mahelka, Jan Bartoš, Jaroslav Doležel, Beat Boller Frequent occurrence of triploid hybrids Festuca pratensis × F. apennina in the Swiss Alps, Alpine Botany 128, no.22 (May 2018): 121–132.https://doi.org/10.1007/s00035-018-0204-7Kathleen M. Kay, Suzie Woolhouse, Brett A. Smith, Nathaniel S. Pope, Nishanta Rajakaruna Sympatric serpentine endemic Monardella (Lamiaceae) species maintain habitat differences despite hybridization, Molecular Ecology 27, no.99 (Apr 2018): 2302–2316.https://doi.org/10.1111/mec.14582M. Möller Nuclear DNA C-values are correlated with pollen size at tetraploid but not diploid level and linked to phylogenetic descent in Streptocarpus (Gesneriaceae), South African Journal of Botany 114 (Jan 2018): 323–344.https://doi.org/10.1016/j.sajb.2017.11.017Geert van Geest, Roeland E Voorrips, Danny Esselink, Aike Post, Richard GF Visser, Paul Arens Conclusive evidence for hexasomic inheritance in chrysanthemum based on analysis of a 183 k SNP array, BMC Genomics 18, no.11 (Aug 2017).https://doi.org/10.1186/s12864-017-4003-0Keisha D. Carlson, Noe Fernandez-Pozo, Aureliano Bombarely, Rahul Pisupati, Lukas A. Mueller, Andreas Madlung Natural variation in stress response gene activity in the allopolyploid Arabidopsis suecica, BMC Genomics 18, no.11 (Aug 2017).https://doi.org/10.1186/s12864-017-4067-xReiner A. Veitia Gene Duplicates: Agents of Fragility? – A Reply to Landry and Diss, Trends in Genetics 33, no.1010 (Oct 2017): 658–660.https://doi.org/10.1016/j.tig.2017.07.013Amber L. Scott, Phillip A. Richmond, Robin D. Dowell, Anna M. Selmecki The Influence of Polyploidy on the Evolution of Yeast Grown in a Sub-Optimal Carbon Source, Molecular Biology and Evolution 34, no.1010 (Jul 2017): 2690–2703.https://doi.org/10.1093/molbev/msx205J. M. Coughlan, S. Han, S. Stefanović, T. A. Dickinson Widespread generalist clones are associated with range and niche expansion in allopolyploids of Pacific Northwest Hawthorns ( Crataegus L.), Molecular Ecology 26, no.2020 (Sep 2017): 5484–5499.https://doi.org/10.1111/mec.14331Wenguang Sun, Xiangguang Ma, Jianwen Zhang, Fuming Su, Yonghong Zhang, Zhimin Li Karyotypes of nineteen species of Asteraceae in the Hengduan Mountains and adjacent regions, Plant Diversity 39, no.44 (Aug 2017): 194–201.https://doi.org/10.1016/j.pld.2017.08.001Zuzana Münzbergová Colchicine application significantly affects plant performance in the second generation of synthetic polyploids and its effects vary between populations, Annals of Botany 120, no.22 (Jun 2017): 329–339.https://doi.org/10.1093/aob/mcx070Ambika Kamath, Rachel A. Levin, Jill S. Miller Floral size and shape evolution following the transition to gender dimorphism, American Journal of Botany 104, no.33 (Mar 2017): 451–460.https://doi.org/10.3732/ajb.1600442Guanjing Hu, Ran Hovav, Corrinne E. Grover, Adi Faigenboim-Doron, Noa Kadmon, Justin T. Page, Joshua A. Udall, Jonathan F. Wendel Evolutionary Conservation and Divergence of Gene Coexpression Networks in Gossypium (Cotton) Seeds, Genome Biology and Evolution (Jan 2017): evw280.https://doi.org/10.1093/gbe/evw280Tanvir-Ul-Hassan Dar, Reiaz-Ul Rehman Introduction to Polyploidy, (Nov 2017): 1–13.https://doi.org/10.1007/978-81-322-3772-3_1Chien-Hsun Huang, Caifei Zhang, Mian Liu, Yi Hu, Tiangang Gao, Ji Qi, Hong Ma Multiple Polyploidization Events across Asteraceae with Two Nested Events in the Early History Revealed by Nuclear Phylogenomics, Molecular Biology and Evolution 33, no.1111 (Sep 2016): 2820–2835.https://doi.org/10.1093/molbev/msw157Michael S. Barker, Brian C. Husband, J. Chris Pires Spreading Winge and flying high: The evolutionary importance of polyploidy after a century of study, American Journal of Botany 103, no.77 (Jul 2016): 1139–1145.https://doi.org/10.3732/ajb.1600272Robert G. Laport, Robert L. Minckley, Justin Ramsey Ecological distributions, phenological isolation, and genetic structure in sympatric and parapatric populations of the Larrea tridentata polyploid complex, American Journal of Botany 103, no.77 (Jul 2016): 1358–1374.https://doi.org/10.3732/ajb.1600105Ezgi Ogutcen, Jana C. Vamosi A phylogenetic study of the tribe Antirrhineae: Genome duplications and long-distance dispersals from the Old World to the New World, American Journal of Botany 103, no.66 (Jun 2016): 1071–1081.https://doi.org/10.3732/ajb.1500464Joseph P. Gallagher, Corrinne E. Grover, Guanjing Hu, Jonathan F. Wendel Insights into the Ecology and Evolution of Polyploid Plants through Network Analysis, Molecular Ecology 25, no.1111 (May 2016): 2644–2660.https://doi.org/10.1111/mec.13626Andrew Lloyd, Kirsten Bomblies Meiosis in autopolyploid and allopolyploid Arabidopsis, Current Opinion in Plant Biology 30 (Apr 2016): 116–122.https://doi.org/10.1016/j.pbi.2016.02.004Ting-Shen Han, Qiong Wu, Xing-Hui Hou, Zi-Wen Li, Yu-Pan Zou, Song Ge, Ya-Long Guo Frequent Introgressions from Diploid Species Contribute to the Adaptation of the Tetraploid Shepherd’s Purse (Capsella bursa-pastoris), Molecular Plant 8, no.33 (Mar 2015): 427–438.https://doi.org/10.1016/j.molp.2014.11.016Nathalie Gontier Reticulate Evolution Everywhere, (Jul 2015): 1–40.https://doi.org/10.1007/978-3-319-16345-1_1Kelsey L. Glennon, Sheri A. Church Gene flow contributes to genetic diversity of tetraploid populations of the North American plant genus Houstonia (Rubiaceae), Rhodora 117, no.969969 (Jan 2015): 41–66.https://doi.org/10.3119/14-10Jennifer M. Coughlan, Saša Stefanović, Timothy A. Dickinson, Mark Carine Relative resource allocation to dispersal and competition demonstrates the putative role of hybridity in geographical parthenogenesis, Journal of Biogeography 41, no.88 (Apr 2014): 1603–1613.https://doi.org/10.1111/jbi.12316Feifei Li, Qiang Fan, Qingyan Li, Sufang Chen, Wei Guo, Dafang Cui, Wenbo Liao Molecular phylogeny of Cotoneaster (Rosaceae) inferred from nuclear ITS and multiple chloroplast sequences, Plant Systematics and Evolution 300, no.66 (Jan 2014): 1533–1546.https://doi.org/10.1007/s00606-014-0980-5Kirsten Bomblies, Andreas Madlung Polyploidy in the Arabidopsis genus, Chromosome Research 22, no.22 (May 2014): 117–134.https://doi.org/10.1007/s10577-014-9416-xB K Mable Polyploids and hybrids in changing environments: winners or losers in the struggle for adaptation?, Heredity 110, no.22 (Jan 2013): 95–96.https://doi.org/10.1038/hdy.2012.105Hanna Weiss-Schneeweiss, Gerald M. Schneeweiss Karyotype Diversity and Evolutionary Trends in Angiosperms, (Aug 2012): 209–230.https://doi.org/10.1007/978-3-7091-1160-4_13Karen E. Mock, Colin M. Callahan, M. Nurul Islam-Faridi, John D. Shaw, Hardeep S. Rai, Stewart C. Sanderson, Carol A. Rowe, Ronald J. Ryel, Michael D. Madritch, Richard S. Gardner, Paul G. Wolf, Randall P. Niedz Widespread Triploidy in Western North American Aspen (Populus tremuloides), PLoS ONE 7, no.1010 (Oct 2012): e48406.https://doi.org/10.1371/journal.pone.0048406Zoe T. Richards, Madeleine. J. H. van Oppen Rarity and genetic diversity in Indo-Pacific Acropora corals, Ecology and Evolution 2, no.88 (Jul 2012): 1867–1888.https://doi.org/10.1002/ece3.304Laís Angélica Borges, Luiz Gustavo Rodrigues Souza, Marcelo Guerra, Isabel Cristina Machado, Gwilym P. Lewis, Ariadna Valentina Lopes Reproductive isolation between diploid and tetraploid cytotypes of Libidibia ferrea (= Caesalpinia ferrea) (Leguminosae): ecological and taxonomic implications, Plant Systematics and Evolution 298, no.77 (May 2012): 1371–1381.https://doi.org/10.1007/s00606-012-0643-3Patrick J. McIntyre Polyploidy associated with altered and broader ecological niches in the Claytonia perfoliata (Portulacaceae) species complex, American Journal of Botany 99, no.44 (Apr 2012): 655–662.https://doi.org/10.3732/ajb.1100466Lucas Majure, Walter Judd, Pam Soltis, Doug Soltis Cytogeography of the Humifusa clade of Opuntia s.s. Mill. 1754 (Cactaceae, Opuntioideae, Opuntieae): correlations with pleistocene refugia and morphological traits in a polyploid complex, Comparative Cytogenetics 6, no.11 (Feb 2012): 53–77.https://doi.org/10.3897/compcytogen.v6i1.2523Mika Bendiksby, Andreas Tribsch, Liv Borgen, Pavel Trávníček, Anne K. Brysting Allopolyploid origins of the Galeopsis tetraploids - revisiting Müntzing’s classical textbook example using molecular tools, New Phytologist 191, no.44 (May 2011): 1150–1167.https://doi.org/10.1111/j.1469-8137.2011.03753.xPamela S. Soltis, J. Gordon Burleigh, Andre S. Chanderbali, Mi-Jeong Yoo, Douglas E. Soltis Gene and Genome Duplications in Plants, (Mar 2011): 269–298.https://doi.org/10.1002/9780470619902.ch15Hong Yao, Akio Kato, Brian Mooney, James A. Birchler Phenotypic and gene expression analyses of a ploidy series of maize inbred Oh43, Plant Molecular Biology 75, no.33 (Dec 2010): 237–251.https://doi.org/10.1007/s11103-010-9722-4Joe Cain Rethinking the Synthesis Period in Evolutionary Studies, Journal of the History of Biology 42, no.44 (Oct 2009): 621–648.https://doi.org/10.1007/s10739-009-9206-zHarald Meimberg, Kevin J. Rice, Neil F. Milan, Collins C. Njoku, John K. McKay Multiple origins promote the ecological amplitude of allopolyploid Aegilops (Poaceae), American Journal of Botany 96, no.77 (Jul 2009): 1262–1273.https://doi.org/10.3732/ajb.0800345Pamela S. Soltis, Douglas E. Soltis The Role of Hybridization in Plant Speciation, Annual Review of Plant Biology 60, no.11 (Jun 2009): 561–588.https://doi.org/10.1146/annurev.arplant.043008.092039D. E. Soltis, V. A. Albert, J. Leebens-Mack, C. D. Bell, A. H. Paterson, C. Zheng, D. Sankoff, C. W. dePamphilis, P. K. Wall, P. S. Soltis Polyploidy and angiosperm diversification, American Journal of Botany 96, no.11 (Jan 2009): 336–348.https://doi.org/10.3732/ajb.0800079David J. Walker, Pascual Romero, Aránzazu de Hoyos, Enrique Correal Seasonal changes in cold tolerance, water relations and accumulation of cations and compatible solutes in Atriplex halimus L., Environmental and Experimental Botany 64, no.33 (Dec 2008): 217–224.https://doi.org/10.1016/j.envexpbot.2008.05.012Václav Mahelka, Judith Fehrer, František Krahulec, Vlasta Jarolímová Recent Natural Hybridization between Two Allopolyploid Wheatgrasses (Elytrigia, Poaceae): Ecological and Evolutionary Implications, Annals of Botany 100, no.22 (Jun 2007): 249–260.https://doi.org/10.1093/aob/mcm093Richard J. A. Buggs, John R. Pannell ECOLOGICAL DIFFERENTIATION AND DIPLOID SUPERIORITY ACROSS A MOVING PLOIDY CONTACT ZONE, Evolution 61, no.11 (Jan 2007): 125–140.https://doi.org/10.1111/j.1558-5646.2007.00010.xIkechukwu O. Agbagwa ., Bosa E. Okoli . Leaf Epidermal Micromorphology in the Systematics of Abrus (Papilionaceae) in Parts of Tropical West Africa, Asian Journal of Plant Sciences 5, no.11 (Jan 2006): 41–49.https://doi.org/10.3923/ajps.2006.41.49JENNIFER A. TATE, DOUGLAS E. SOLTIS, PAMELA S. SOLTIS Polyploidy in Plants, (Jan 2005): 371–426.https://doi.org/10.1016/B978-012301463-4/50009-7Jennifer A. Tate, Beryl B. Simpson Breeding system evolution in Tarasa (Malvaceae) and selection for reduced pollen grain size in the polyploid species, American Journal of Botany 91, no.22 (Feb 2004): 207–213.https://doi.org/10.3732/ajb.91.2.207Vassiliki Betty Smocovitis G. Ledyard Stebbins and the Evolutionary Synthesis, Annual Review of Genetics 35, no.11 (Dec 2001): 803–814.https://doi.org/10.1146/annurev.genet.35.102401.091525L. L. Sanford, R. S. Kobayashi, K. L. Deahl, S. L. Sinden Diploid and tetraploidSolanum chacoense genotypes that synthesize leptine glycoalkaloids and deter feeding by Colorado potato beetle, American Potato Journal 74, no.11 (Jan 1997): 15–21.https://doi.org/10.1007/BF02849168SHARDA KHANDELWAL Chromosome evolution in the genus Ophioglossum L., Botanical Journal of the Linnean Society 102, no.33 (Jun 2008): 205–217.https://doi.org/10.1111/j.1095-8339.1990.tb01876.xJoel B. Hagen Experimentalists and naturalists in twentieth-century botany: Experimental taxonomy, 1920?1950, Journal of the History of Biology 17, no.22 (Jan 1984): 249–270.https://doi.org/10.1007/BF00143734Joel B. Hagen THE DEVELOPMENT OF EXPERIMENTAL METHODS IN PLANT TAXONOMY, 1920‐1950, TAXON 32, no.33 (Jun 2019): 406–416.https://doi.org/10.2307/1221497Roger W. Sanders, Tod F. Stuessy, Roberto Rodriguez CHROMOSOME NUMBERS FROM THE FLORA OF THE JUAN FERNANDEZ ISLANDS, American Journal of Botany 70, no.66 (Jul 1983): 799–810.https://doi.org/10.1002/j.1537-2197.1983.tb06415.xJames E. Piechura, David E. Fairbrothers THE USE OF PROTEIN‐SEROLOGICAL CHARACTERS IN THE SYSTEMATICS OF THE FAMILY OLEACEAE, American Journal of Botany 70, no.55 (May 1983): 780–789.https://doi.org/10.1002/j.1537-2197.1983.tb12457.xOtto T. Solbrig George Ledyard Stebbins, (Jan 1979): 1–17.https://doi.org/10.1007/978-1-349-04627-0_1A. W. Johnson, J. G. Packer Polyploidy and Environment in Arctic Alaska, Science 148, no.36673667 (Apr 1965): 237–239.https://doi.org/10.1126/science.148.3667.237DAVID D. KECK Trends in Systematic Botany, (Jan 1957): 47–107.https://doi.org/10.1016/B978-1-4832-0002-6.50006-4Emilio Battaglia Urginea Maritima (L.) Baker: Biotipi 2n, 3n, 4n, 6n. e Loro Distribuzione Geografic, Caryologia 9, no.22 (Jan 1957): 293–314.https://doi.org/10.1080/00087114.1957.10797597 Loy V. Crowder Morphological and Cytological Studies in Tall Fescue (Festuca arundinacea Schreb.) and Meadow Fescue (F. elatior L.), Botanical Gazette 117, no.33 (Sep 2015): 214–223.https://doi.org/10.1086/335908E. Lucy Braun The phytogeography of unglaciated Eastern United States and its interpretation, The Botanical Review 21, no.66 (Jun 1955): 297–375.https://doi.org/10.1007/BF02872433Charles H. Uhl, Reid Moran THE CYTOTAXONOMY OF DUDLEYA AND HASSEANTHUS, American Journal of Botany 40, no.77 (Jul 1953): 492–502.https://doi.org/10.1002/j.1537-2197.1953.tb06510.xVerne Grant THE ROLE OF HYBRIDIZATION IN THE EVOLUTION OF THE LEAFY-STEMMED GILIAS, Evolution 7, no.11 (May 2017): 51–64.https://doi.org/10.1111/j.1558-5646.1953.tb00058.xGordon Haskell pH tolerance and polyploidy in angiosperms, Plant and Soil 3, no.33 (Jul 1951): 223–238.https://doi.org/10.1007/BF01393978L. O. Gaiser CHROMOSOME STUDIES IN LIATRIS III. PUNCTATAE, American Journal of Botany 37, no.99 (Nov 1950): 763–777.https://doi.org/10.1002/j.1537-2197.1950.tb11069.x Henry W. Jensen Meiosis in an Unusual Form of Aconitum uncinatum L., The American Naturalist 84, no.814814 (Oct 2015): 17–22.https://doi.org/10.1086/281609Charles B. Heiser Natural hybridization with particular reference to introgression, The Botanical Review 15, no.1010 (Dec 1949): 645–687.https://doi.org/10.1007/BF02861577Friedrich Ehrendorfer Zur Phylogenie der GattungGalium. I, Osterreichische Botanische Zeitschrift 96, no.11 (Mar 1949): 109–138.https://doi.org/10.1007/BF01252342H. H. Allan Wild species-hybrids in the phanerogams. II, The Botanical Review 15, no.22 (Feb 1949): 77–105.https://doi.org/10.1007/BF02861774Raymond J. Moore CYTOTAXONOMIC STUDIES IN THE LOGANIACEAE. I. CHROMOSOME NUMBERS AND PHYLOGENY IN THE LOGANIACEAE, American Journal of Botany 34, no.1010 (Dec 1947): 527–538.https://doi.org/10.1002/j.1537-2197.1947.tb13026.xW. M. Myers Cytology and genetics of forage grasses, The Botanical Review 13, no.77 (Jul 1947): 369–421.https://doi.org/10.1007/BF02861822G. Ledyard Stebbins Types of Polyploids: Their Classification and Significance, (Jan 1947): 403–429.https://doi.org/10.1016/S0065-2660(08)60490-3Shao-Lin Chen, P. S. Tang STUDIES ON COLCHICINE-INDUCED AUTOTETRAPLOID BARLEY.: III. PHYSIOLOGICAL STUDIES, American Journal of Botany 32, no.44 (Apr 1945): 177–179.https://doi.org/10.1002/j.1537-2197.1945.tb05104.xShao-lin Chen, Shu-min Shen, P. S. Tang STUDIES ON COLCHICINE-INDUCED AUTOTETRAPLOID BARLEY. I AND II. CYTOLOGICAL AND MORPHOLOGICAL OBSERVATIONS, American Journal of Botany 32, no.33 (Mar 1945): 103–106.https://doi.org/10.1002/j.1537-2197.1945.tb05092.xROBERT LAMM CYTOGENETIC STUDIES IN SOLANUM, SECT. TUBERARIUM, Hereditas 31, no.1-21-2 (Jul 2010): 1–128.https://doi.org/10.1111/j.1601-5223.1945.tb02750.xBruce A. Perry CHROMOSOME NUMBER AND PHYLOGENETIC RELATIONSHIPS IN THE EUPHORB ACEAE, American Journal of Botany 30, no.77 (Jul 1943): 527–543.https://doi.org/10.1002/j.1537-2197.1943.tb14796.xS. G. Stephens Colchicine-produced polyploids inGossypium, Journal of Genetics 44, no.2-32-3 (Dec 1942): 272–295.https://doi.org/10.1007/BF02982832Hugh M. Raup Trends in the Development of Geographic Botany, Annals of the Association of American Geographers 32, no.44 (Dec 1942): 319–354.https://doi.org/10.1080/00045604209357239G. Tischler Polyploidie und Artbildung, Die Naturwissenschaften 30, no.48-4948-49 (Nov 1942): 713–718.https://doi.org/10.1007/BF01488992O. J. Eigsti A CYTOLOGICAL INVESTIGATION OF POLYGONATUM USING THE COLCHICINE-POLLEN TUBE TECHNIQUE, American Journal of Botany 29, no.88 (Oct 1942): 626–636.https://doi.org/10.1002/j.1537-2197.1942.tb10258.xNorman H. Giles AUTOPOLYPLOIDY AND GEOGRAPHICAL DISTRIBUTION IN CUTHBERTIA GRAMINEA SMALL, American Journal of Botany 29, no.88 (Oct 1942): 637–645.https://doi.org/10.1002/j.1537-2197.1942.tb10259.xT. H. Goodspeed, Muriel V. Bradley Amphidiploidy, The Botanical Review 8, no.55 (May 1942): 271–316.https://doi.org/10.1007/BF02882226ÅKE GUSTAFSSON THE ORIGIN AND PROPERTIES OF THE EUROPEAN BLACKBERRY FLORA, Hereditas 28, no.3-43-4 (Jul 2010): 249–277.https://doi.org/10.1111/j.1601-5223.1942.tb03279.xErnest B. Babcock Systematics, cytogenetics and evolution in Crepis, The Botanical Review 8, no.33 (Mar 1942): 139–190.https://doi.org/10.1007/BF02888401 G. Ledyard Stebbins, Jr. Polyploid Complexes in Relation to Ecology and the History of Floras, The American Naturalist 76, no.762762 (Oct 2015): 36–45.https://doi.org/10.1086/281012 C. L. Huskins Polyploidy and Mutations, The American Naturalist 75, no.759759 (Oct 2015): 329–346.https://doi.org/10.1086/280968Hugh M. Raup Botanical problems in boreal America. II, The Botanical Review 7, no.44 (Apr 1941): 209–248.https://doi.org/10.1007/BF02872453J. M. Webber Polyembryony, The Botanical Review 6, no.1111 (Nov 1940): 575–598.https://doi.org/10.1007/BF02919556George L. Church CYTOTAXONOMIC STUDIES IN THE GRAMINEAE SPARTINA, ANDROPOGON AND PANICUM, American Journal of Botany 27, no.44 (Apr 1940): 263–271.https://doi.org/10.1002/j.1537-2197.1940.tb14682.x
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