Artigo Revisado por pares

Selection for Outcrossing, Sexual Selection, and the Evolution of Dioecy in Plants

1981; University of Chicago Press; Volume: 118; Issue: 3 Linguagem: Inglês

10.1086/283837

ISSN

1537-5323

Autores

James D. Thomson,

Tópico(s)

Plant Parasitism and Resistance

Resumo

Previous articleNext article No AccessNotes and CommentsSelection for Outcrossing, Sexual Selection, and the Evolution of Dioecy in PlantsJames D. Thomson, and Spencer C. H. BarrettJames D. Thomson Search for more articles by this author , and Spencer C. H. Barrett Search for more articles by this author PDFPDF PLUS Add to favoritesDownload CitationTrack CitationsPermissionsReprints Share onFacebookTwitterLinkedInRedditEmail SectionsMoreDetailsFiguresReferencesCited by The American Naturalist Volume 118, Number 3Sep., 1981 Published for The American Society of Naturalists Article DOIhttps://doi.org/10.1086/283837 Views: 56Total views on this site Citations: 131Citations are reported from Crossref Copyright 1981 The University of ChicagoPDF download Crossref reports the following articles citing this article:Rafael F. del Castillo and Sonia Trujillo-Argueta Heterospecific Pollen Transfer, Self-Assurance, and the Distribution of Dioecy and Hermaphroditism in a Single Species: The Importance of Pollen Landscapes, International Journal of Plant Sciences 183, no.88 (Aug 2022): 664–673.https://doi.org/10.1086/721652Indiara Nunes Mesquita Ferreira, Raysa Kristine de Oliveira Cavalcante, João Paulo Raimundo Borges, Tamara Poliana de Oliveira Teixeira, Daniel Paiva Silva, Túlio Sá, Edivani Villaron Franceschinelli Two dioecious Simarouba species with a specialized pollination system and low reproductive efficacy in Central Brazil, Rodriguésia 73 (Jan 2022).https://doi.org/10.1590/2175-7860202273030Ebenézer B. 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Leonard The Evolution of Sexual Systems in Animals, (May 2019): 1–58.https://doi.org/10.1007/978-3-319-94139-4_1Sookyung Shin, Sang Gil Lee, Hyesoon Kang Spatial distribution patterns of old-growth forest of dioecious tree Torreya nucifera in rocky Gotjawal terrain of Jeju Island, South Korea, Journal of Ecology and Environment 41, no.11 (Aug 2017).https://doi.org/10.1186/s41610-017-0050-3Jos Käfer, Gabriel A. B. Marais, John R. Pannell On the rarity of dioecy in flowering plants, Molecular Ecology 26, no.55 (Feb 2017): 1225–1241.https://doi.org/10.1111/mec.14020Mao-Sheng Chen, Bang-Zhen Pan, Qiantang Fu, Yan-Bin Tao, Jorge Martínez-Herrera, Longjian Niu, Jun Ni, Yuling Dong, Mei-Li Zhao, Zeng-Fu Xu Comparative Transcriptome Analysis between Gynoecious and Monoecious Plants Identifies Regulatory Networks Controlling Sex Determination in Jatropha curcas, Frontiers in Plant Science 7 (Jan 2017).https://doi.org/10.3389/fpls.2016.01953Lior Glick, Niv Sabath, Tia-Lynn Ashman, Emma Goldberg, Itay Mayrose Polyploidy and sexual system in angiosperms: Is there an association?, American Journal of Botany 103, no.77 (Jun 2016): 1223–1235.https://doi.org/10.3732/ajb.1500424Niv Sabath, Emma E. Goldberg, Lior Glick, Moshe Einhorn, Tia‐Lynn Ashman, Ray Ming, Sarah P. Otto, Jana C. Vamosi, Itay Mayrose Dioecy does not consistently accelerate or slow lineage diversification across multiple genera of angiosperms, New Phytologist 209, no.33 (Oct 2015): 1290–1300.https://doi.org/10.1111/nph.13696Gregory J. Anderson, Mona K. J. Anderson, Nikisha Patel The ecology, evolution, and biogeography of dioecy in the genus Solanum : With paradigms from the strong dioecy in Solanum polygamum , to the unsuspected and cryptic dioecy in Solanum conocarpum, American Journal of Botany 102, no.33 (Mar 2015): 471–486.https://doi.org/10.3732/ajb.1400486Rachel A. Levin, Edmund M. Keyes, Jill S. Miller, and Evolutionary Relationships, Gynodioecy, and Polyploidy in the Galápagos Endemic Lycium minimum (Solanaceae), International Journal of Plant Sciences 176, no.22 (Jun 2015): 197–210.https://doi.org/10.1086/679492Brian J. Vincent, Sarah Barrett, Anne Cochrane, Julie A. Plummer, Michael Renton Conservation biology of two endemic Beyeria species (Euphorbiaceae) from southern Western Australia, Australian Journal of Botany 63, no.66 (Jan 2015): 484.https://doi.org/10.1071/BT14310Caitlin M. Blank, Rachel A. Levin, Jill S. Miller Intraspecific variation in gender strategies in Lycium (Solanaceae): Associations with ploidy and changes in floral form following the evolution of gender dimorphism, American Journal of Botany 101, no.1212 (Dec 2014): 2160–2168.https://doi.org/10.3732/ajb.1400356S. S. Renner The relative and absolute frequencies of angiosperm sexual systems: Dioecy, monoecy, gynodioecy, and an updated online database, American Journal of Botany 101, no.1010 (Sep 2014): 1588–1596.https://doi.org/10.3732/ajb.1400196Charles S.P. Foster, Simon Y.W. Ho, Barry J. Conn, Murray J. Henwood Molecular systematics and biogeography of Logania R.Br. (Loganiaceae), Molecular Phylogenetics and Evolution 78 (Sep 2014): 324–333.https://doi.org/10.1016/j.ympev.2014.06.001Xing-Nan Zhao, Sheng-Jun Huang, Ji-Min Zhao, Yan-Wen Zhang Gender Variation in a Monoecious Woody Vine Schisandra chinensis (Schisandraceae) in Northeast China, Annales Botanici Fennici 50, no.44 (Aug 2013): 209–219.https://doi.org/10.5735/086.050.0402Jordan P. Sinclair, Glenn D. Maxwell, D. Carl Freeman Consanguineous mating, specialization, and the environment: How multiple variable interactions affect the evolution of dioecy, American Journal of Botany 100, no.66 (Jun 2013): 1038–1049.https://doi.org/10.3732/ajb.1200579H. Kapua Kawelo, Susan Ching Harbin, Stephanie M. Joe, Matthew J. Keir, Lauren Weisenberger Unique Reintroduction Considerations in Hawaii: Case Studies from a Decade of Rare Plant Restoration at the Oahu Army Natural Resource Rare Plant Program, (Jan 2012): 209–226.https://doi.org/10.5822/978-1-61091-183-2_12Felipe Wanderley Amorim, Clesnan Mendes-Rodrigues, Pietro Kiyoshi Maruyama, Paulo Eugênio Oliveira, , Sexual ratio and floral biology of the dioecious Neea theifera Oerst. (Nyctaginaceae) in a cerrado rupestre of central Brazil, Acta Botanica Brasilica 25, no.44 (Dec 2011): 785–792.https://doi.org/10.1590/S0102-33062011000400006Jérémy Migliore, Alex Baumel, Marianick Juin, Katia Diadema, Laetitia Hugot, Régine Verlaque, Frédéric Médail Genetic diversity and structure of a Mediterranean endemic plant in Corsica (Mercurialis corsica, Euphorbiaceae), Population Ecology 53, no.44 (Feb 2011): 573–586.https://doi.org/10.1007/s10144-011-0266-5Laura B. Vary, Daniel L. Gillen, Miramasonadro Randrianjanahary, Porter P. Lowry, Ann K. Sakai, Stephen G. Weller Dioecy, Monoecy, and Their Ecological Correlates in the Littoral Forest of Madagascar, Biotropica 43, no.55 (Jan 2011): 582–590.https://doi.org/10.1111/j.1744-7429.2010.00742.xRowan H. Brookes and Linley K. Jesson Do Pollen and Ovule Number Match the Mating Environment? An Examination of Temporal Change in a Population of Stylidium armeria Brookes & Jesson, International Journal of Plant Sciences 171, no.88 (Jul 2015): 818–827.https://doi.org/10.1086/655770LIANGHUA CHEN, SHENG ZHANG, HONGXIA ZHAO, HELENA KORPELAINEN, CHUNYANG LI Sex-related adaptive responses to interaction of drought and salinity in Populus yunnanensis, Plant, Cell & Environment 33, no.1010 (Sep 2010): 1767–1778.https://doi.org/10.1111/j.1365-3040.2010.02182.xMarcos Méndez, Jérôme Munzinger Planchonella, first record of gynomonoecy for the family Sapotaceae, Plant Systematics and Evolution 287, no.1-21-2 (Apr 2010): 65–73.https://doi.org/10.1007/s00606-010-0290-5Marcel E. Dorken Sex ratio variation in gynodioecious species of Echium endemic to the Canary Islands, Botany 88, no.22 (Feb 2010): 211–216.https://doi.org/10.1139/B09-106Rebecca H. Penny, Janet C. Steven Sexual dimorphism in pollen grain size in cryptically dioecious Thalictrum macrostylum, Plant Systematics and Evolution 279, no.1-41-4 (Mar 2009): 11–19.https://doi.org/10.1007/s00606-008-0114-zSimon A. Queenborough, Susan J. Mazer, Steven M. Vamosi, Nancy C. Garwood, Renato Valencia, Rob P. Freckleton Seed mass, abundance and breeding system among tropical forest species: do dioecious species exhibit compensatory reproduction or abundances?, Journal of Ecology 97, no.33 (May 2009): 555–566.https://doi.org/10.1111/j.1365-2745.2009.01485.xSara López-Vinyallonga, Iraj Mehregan, Núria Garcia-Jacas, Olga Tscherneva, Alfonso Susanna, Joachim W. Kadereit Phylogeny and evolution of the Arctium-Cousinia complex (Compositae, Cardueae-Carduinae), TAXON 58, no.11 (Feb 2009): 153–171.https://doi.org/10.1002/tax.581016Cyril Guibert, Laure Civeyrel, Peter Linder Male and female separation event trapped in a species tree, TAXON 58, no.11 (Feb 2009): 172–180.https://doi.org/10.1002/tax.581017Christopher T. Martine, Gregory J. Anderson, Donald H. Les Gender-bending aubergines: molecular phylogenetics of cryptically dioecious Solanum in Australia, Australian Systematic Botany 22, no.22 (Jan 2009): 107.https://doi.org/10.1071/SB07039Kara PRZECZEK, Carla MUELLER, Steven M. VAMOSI The evolution of aposematism is accompanied by increased diversification, Integrative Zoology 3, no.33 (Sep 2008): 149–156.https://doi.org/10.1111/j.1749-4877.2008.00091.xSteven M. Vamosi, Susan J. Mazer, Fernando Cornejo BREEDING SYSTEMS AND SEED SIZE IN A NEOTROPICAL FLORA: TESTING EVOLUTIONARY HYPOTHESES, Ecology 89, no.99 (Sep 2008): 2461–2472.https://doi.org/10.1890/07-0674.1Michael S. Kinney, J. Travis Columbus, Elizabeth A. Friar Unisexual flower, spikelet, and inflorescence development in monoecious/dioecious Bouteloua dimorpha (Poaceae, Chloridoideae), American Journal of Botany 95, no.22 (Feb 2008): 123–132.https://doi.org/10.3732/ajb.95.2.123A. M. Allen, S. J. Hiscock Evolution and Phylogeny of Self-Incompatibility Systems in Angiosperms, (Jan 2008): 73–101.https://doi.org/10.1007/978-3-540-68486-2_4Jill S. Miller, John L. Stanton-Geddes Gynodioecy in Lobelia Siphilitica and L. Spicata (Lobeliaceae) from Western Massachusetts 1, The Journal of the Torrey Botanical Society 134, no.33 (Jul 2007): 349–361.https://doi.org/10.3159/1095-5674(2007)134[349:GILSAL]2.0.CO;2Anna Traveset, Anna Jakobsson Ecology of Plant Reproduction, (Dec 2009).https://doi.org/10.1201/9781420007626.ch17ANGELA J. BEAUMONT, TREVOR J. EDWARDS, FRANCOIS R. SMITH The first record of gynodioecy in a species of Gnidia (Thymelaeaceae) from South Africa, Botanical Journal of the Linnean Society 152, no.22 (Oct 2006): 219–233.https://doi.org/10.1111/j.1095-8339.2006.00566.xGregory J. Anderson, Gabriel Bernardello, Matthew R. Opel, Arnoldo Santos‐Guerra, Mona Anderson Reproductive biology of the dioecious Canary Islands endemic Withania aristata (Solanaceae), American Journal of Botany 93, no.99 (Sep 2006): 1295–1305.https://doi.org/10.3732/ajb.93.9.1295John R. Pannell, Miguel Verdú THE EVOLUTION OF GENDER SPECIALIZATION FROM DIMORPHIC HERMAPHRODITISM: PATHS FROM HETERODICHOGAMY TO GYNODIOECY AND ANDRODIOECY, Evolution 60, no.44 (Jan 2006): 660.https://doi.org/10.1554/05-481.1Darren J. Obbard, Stephen A. Harris, Richard J. A. Buggs, John R. Pannell HYBRIDIZATION, POLYPLOIDY, AND THE EVOLUTION OF SEXUAL SYSTEMS IN MERCURIALIS (EUPHORBIACEAE), Evolution 60, no.99 (Jan 2006): 1801.https://doi.org/10.1554/06-104.1Caroline H. Mitchell, Pamela K. Diggle The evolution of unisexual flowers: morphological and functional convergence results from diverse developmental transitions, American Journal of Botany 92, no.77 (Jul 2005): 1068–1076.https://doi.org/10.3732/ajb.92.7.1068Linda Newstrom, Alastair Robertson Progress in understanding pollination systems in New Zealand, New Zealand Journal of Botany 43, no.11 (Jan 2005): 1–59.https://doi.org/10.1080/0028825X.2005.9512943Sébastien Barot, Jacques Gignoux How do sessile dioecious species cope with their males?, Theoretical Population Biology 66, no.33 (Nov 2004): 163–173.https://doi.org/10.1016/j.tpb.2004.05.002 W. G. Wilson and L. D. Harder Reproductive Uncertainty and the Relative Competitiveness of Simultaneous Hermaphroditism versus Dioecy. W. G. Wilson and L. D. Harder, The American Naturalist 162, no.22 (Jul 2015): 220–241.https://doi.org/10.1086/376584Jill S. Miller, D. Lawrence Venable The transition to gender dimorphism on an evolutionary background of self‐incompatibility: an example from Lycium (Solanaceae), American Journal of Botany 89, no.1212 (Dec 2002): 1907–1915.https://doi.org/10.3732/ajb.89.12.1907 Tetsuto Abe , Naoko Yamashita , Nobuyuki Tanaka , and Hiromichi Kushima Sex Ratio Variation of Bischofia javanica Bl. (Euphorbiaceae) between Native Habitat, Okinawa (Ryukyu Islands), and Invaded Habitat, Ogasawara (Bonin Islands) Abe et al., International Journal of Plant Sciences 163, no.66 (Jul 2015): 1011–1016.https://doi.org/10.1086/342631Adriana Paula Fuzeto, Ana Angélica Almeida Barbosa, Cecília Lomônaco, , Cabralea canjerana subsp. polytricha (Adri. Juss.) Penn. (Meliaceae), uma espécia diótica, Acta Botanica Brasilica 15, no.22 (Aug 2001): 167–175.https://doi.org/10.1590/S0102-33062001000200003T. B. H. Reusch Fitness-consequences of geitonogamous selfing in a clonal marine angiosperm ( Zostera marina ), Journal of Evolutionary Biology 14, no.11 (Dec 2001): 129–138.https://doi.org/10.1046/j.1420-9101.2001.00257.xDeborah Charlesworth Evolution: An exception that proves the rule, Current Biology 11, no.11 (Jan 2001): R13–R15.https://doi.org/10.1016/S0960-9822(00)00035-XMargot R. Bram, James A. Quinn Sex expression, sex-specific traits, and the effects of salinity on growth and reproduction of Amaranthus cannabinus (Amaranthaceae), a dioecious annual, American Journal of Botany 87, no.1111 (Nov 2000): 1609–1618.https://doi.org/10.2307/2656737 Jana C. Heilbuth Lower Species Richness in Dioecious Clades. J. C. Heilbuth, The American Naturalist 156, no.33 (Jul 2015): 221–241.https://doi.org/10.1086/303389 George D. Weiblen , Ryan K. Oyama , and Michael J. Donoghue Phylogenetic Analysis of Dioecy in Monocotyledons. G. D. Weiblen et al., The American Naturalist 155, no.11 (Jul 2015): 46–58.https://doi.org/10.1086/303303Germán Avila-Sakar, César A. Domínguez PARENTAL EFFECTS AND GENDER SPECIALIZATION IN A TROPICAL HETEROSTYLOUS SHRUB, Evolution 54, no.33 (Jan 2000): 866.https://doi.org/10.1554/0014-3820(2000)054[0866:PEAGSI]2.3.CO;2Neil W. Sawyer, Gregory J. Anderson Dioecy in South American Deprea (Solanaceae)1, BIOTROPICA 32, no.22 (Jan 2000): 291.https://doi.org/10.1646/0006-3606(2000)032[0291:DISADS]2.0.CO;2Laurence Humeau, Thierry Pailler, John D. Thompson Variation in Gender and Flower-Size Dimorphism in the Dioecious Tree Dombeya ciliata, an Endemic to La Réunion Island1, BIOTROPICA 32, no.33 (Jan 2000): 463.https://doi.org/10.1646/0006-3606(2000)032[0463:VIGAFS]2.0.CO;2Tia-Lynn Ashman, M. A. Geber, T. E. Dawson, L. F. Delph A Prescription for Gender Study in the Next Century, American Journal of Botany 87, no.11 (Jan 2000): 147.https://doi.org/10.2307/2656693Laurence Humeau, Thierry Pailler, John D. Thompson Cryptic Dioecy and Leaky Dioecy in Endemic Species of Dombeya (Sterculiaceae) on La Reunion, American Journal of Botany 86, no.1010 (Oct 1999): 1437.https://doi.org/10.2307/2656925C. J. Webb, David G. Lloyd, Lynda F. Delph Gender dimorphism in indigenous New Zealand seed plants, New Zealand Journal of Botany 37, no.11 (Mar 1999): 119–130.https://doi.org/10.1080/0028825X.1999.9512618Ann K. Sakai, Stephen G. Weller Gender and Sexual Dimorphism in Flowering Plants: A review of Terminology, Biogeographic Patterns, Ecological Correlates, and Phylogenetic Approaches, (Jan 1999): 1–31.https://doi.org/10.1007/978-3-662-03908-3_1Colin J. Webb Empirical Studies: Evolution and Maintenance of Dimorphic Breeding Systems, (Jan 1999): 61–95.https://doi.org/10.1007/978-3-662-03908-3_3T. J. De Jong, Klinkhamer, Rademaker How geitonogamous selfing affects sex allocation in hermaphrodite plants, Journal of Evolutionary Biology 12, no.11 (Jun 2008): 166–176.https://doi.org/10.1046/j.1420-9101.1999.00001.xThierry Pailler, Laurence Humeau, Jacques Figier, John D. Thompson Reproductive trait variation in the functionally dioecious and morphologically heterostylous island endemic Chassalia corallioides (Rubiaceae), Biological Journal of the Linnean Society 64, no.33 (Jan 2008): 297–313.https://doi.org/10.1111/j.1095-8312.1998.tb00335.xD.M. Percy, Q.C.B. Cronk Conservation in relation to mating system in Nesohedyotis arborea (Rubiaceae), a rare endemic tree from St Helena, Biological Conservation 80, no.22 (May 1997): 135–145.https://doi.org/10.1016/S0006-3207(96)00130-9Tia-Lynn Ashman, Daniel J. Schoen The cost of floral longevity in Clarkia tembloriensis: An experimental investigation, Evolutionary Ecology 11, no.33 (May 1997): 289–300.https://doi.org/10.1023/A:1018416403530John Pannell Widespread functional androdioecy in Mercurialis annua L. (Euphorbiaceae), Biological Journal of the Linnean Society 61, no.11 (Jun 2008): 95–116.https://doi.org/10.1111/j.1095-8312.1997.tb01779.xSabine Lebel-Hardenack, Sarah R. Grant Genetics of sex determination in flowering plants, Trends in Plant Science 2, no.44 (Apr 1997): 130–136.https://doi.org/10.1016/S1360-1385(97)01012-1John Pannell THE MAINTENANCE OF GYNODIOECY AND ANDRODIOECY IN A METAPOPULATION, Evolution 51, no.11 (May 2017): 10–20.https://doi.org/10.1111/j.1558-5646.1997.tb02383.xS. P. DiFazio, M.V. Wilson, N. C. Vance Variation in sex expression of Taxus brevifolia in western Oregon, Canadian Journal of Botany 74, no.1212 (Dec 1996): 1943–1946.https://doi.org/10.1139/b96-232 The reproductive biology and genetics of island plants, Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences 351, no.13411341 (Jan 1997): 725–733.https://doi.org/10.1098/rstb.1996.0067Lynda F. Delph, David G. Lloyd Inbreeding depression in the gynodioecious shrub Hebe subalpina (Scrophulahaceae), New Zealand Journal of Botany 34, no.22 (Jun 1996): 241–247.https://doi.org/10.1080/0028825X.1996.10410688Io Skogsmyr The effects of sexually selected traits on gene dispersal, Field Crops Research 45, no.1-31-3 (May 1996): 163–170.https://doi.org/10.1016/0378-4290(95)00068-2Stewart T. Schultz, Fred R. Ganders EVOLUTION OF UNISEXUALITY IN THE HAWAIIAN FLORA: A TEST OF MICROEVOLUTIONARY THEORY, Evolution 50, no.22 (May 2017): 842–855.https://doi.org/10.1111/j.1558-5646.1996.tb03893.xN. Machon, V. Deletre-Le Boulc'h, C. Rameau Quantitative analysis of sexual dimorphism in Asparagus, Canadian Journal of Botany 73, no.1111 (Nov 1995): 1780–1786.https://doi.org/10.1139/b95-190Bertrand Dommée, Andrée Biascamano, Nicole Denelle, Jean-Louis Bompar, John D. Thompson Sexual tetramorphism in Thymelaea hirsuta (Thymelaeaceae): morph ratios in open-pollinated progeny, American Journal of Botany 82, no.66 (Jun 1995): 734–740.https://doi.org/10.1002/j.1537-2197.1995.tb15684.xSusanne S. Renner, Robert E. Ricklefs D ioecy and its correlates in the flowering plants, American Journal of Botany 82, no.55 (May 1995): 596–606.https://doi.org/10.1002/j.1537-2197.1995.tb11504.xSandrine Maurice, Eric Belhassen, Denis Couvet, Pierre-Henri Gouyon Evolution of dioecy: can nuclear–cytoplasmic interactions select for maleness?, Heredity 73, no.44 (Oct 1994): 346–354.https://doi.org/10.1038/hdy.1994.181Io Skogsmyr Gene dispersal from transgenic potatoes to conspecifics: a field trial, Theoretical and Applied Genetics 88, no.6-76-7 (Aug 1994): 770–774.https://doi.org/10.1007/BF01253984KRYSTYNA M. URBANSKA Pollen, Mating and Paternity in Agamospermous Angiosperms, Plant Species Biology 9, no.11 (Apr 1994): 57–67.https://doi.org/10.1111/j.1442-1984.1994.tb00083.xS. Lahav-Ginott, Q. C. B. Cronk The mating system ofElatostema (Urticaceae) in relation to morphology: A comparative study, Plant Systematics and Evolution 186, no.3-43-4 (Jan 1993): 135–145.https://doi.org/10.1007/BF00940793M. Timm Hoffman FUNCTIONAL DIOECY IN ECHINOCEREUS COCCINEUS (CACTACEAE): BREEDING SYSTEM, SEX RATIOS, AND GEOGRAPHIC RANGE OF FLORAL DIMORPHISM, American Journal of Botany 79, no.1212 (Dec 1992): 1382–1388.https://doi.org/10.1002/j.1537-2197.1992.tb13748.xMartin T. Morgan ATTRACTIVE STRUCTURES AND THE STABILITY OF HERMAPHRODITIC SEX EXPRESSION IN FLOWERING PLANTS, Evolution 46, no.44 (May 2017): 1199–1213.https://doi.org/10.1111/j.1558-5646.1992.tb00628.xStephanie S. Mayer, Deborah Charlesworth GENETIC EVIDENCE FOR MULTIPLE ORIGINS OF DIOECY IN THE HAWAIIAN SHRUB WIKSTROEMIA (THYMELAEACEAE), Evolution 46, no.11 (May 2017): 207–215.https://doi.org/10.1111/j.1558-5646.1992.tb01995.xJames A. Quinn EVOLUTION OF DIOECY IN BUCHLOE DACTYLOIDES (GRAMINEAE): TESTS FOR SEX-SPECIFIC VEGETATIVE CHARACTERS, ECOLOGICAL DIFFERENCES, AND SEXUAL NICHE-PARTITIONING, American Journal of Botany 78, no.44 (Apr 1991): 481–488.https://doi.org/10.1002/j.1537-2197.1991.tb15214.xTaber D. Allison VARIATION IN SEX EXPRESSION IN CANADA YEW (TAXUS CANADENSIS), American Journal of Botany 78, no.44 (Apr 1991): 569–578.https://doi.org/10.1002/j.1537-2197.1991.tb15223.xVera Aber Krischik, Robert F. Denno Differences in environmental response between the sexes of the dioecious shrub Baccharis halimifolia (Compositae), Oecologia 83, no.22 (Jun 1990): 176–181.https://doi.org/10.1007/BF00317749James D. Thomson, Johanne Brunet Hypotheses for the evolution of dioecy in seed plants, Trends in Ecology & Evolution 5, no.11 (Jan 1990): 11–16.https://doi.org/10.1016/0169-5347(90)90006-YMichael J. Donoghue PHYLOGENIES AND THE ANALYSIS OF EVOLUTIONARY SEQUENCES, WITH EXAMPLES FROM SEED PLANTS, Evolution 43, no.66 (May 2017): 1137–1156.https://doi.org/10.1111/j.1558-5646.1989.tb02565.xTodd E. Dawson, L. C. Bliss Patterns of water use and the tissue water relations in the dioecious shrub, Salix arctica: the physiological basis for habitat partitioning between the sexes, Oecologia 79, no.33 (Aug 2013): 332–343.https://doi.org/10.1007/BF00384312Diane R. Campbell MEASUREMENTS OF SELECTION IN A HERMAPHRODITIC PLANT: VARIATION IN MALE AND FEMALE POLLINATION SUCCESS, Evolution 43, no.22 (May 2017): 318–334.https://doi.org/10.1111/j.1558-5646.1989.tb04230.xMark B. Hessing Variation in self-fertility and floral characters ofGeranium caespitosum (Geraniaceae) along an elevational gradient, Plant Systematics and Evolution 166, no.3-43-4 (Jan 1989): 225–241.https://doi.org/10.1007/BF00935951Kim E. Steiner DIOECISM AND ITS CORRELATES IN THE CAPE FLORA OF SOUTH AFRICA, American Journal of Botany 75, no.1111 (Nov 1988): 1742–1754.https://doi.org/10.1002/j.1537-2197.1988.tb11250.xD. P. STEVENS On the gynodioecious polymorphism in Saxifraga granulata L. (Saxifragaceae), Biological Journal of the Linnean Society 35, no.11 (Jan 2008): 15–28.https://doi.org/10.1111/j.1095-8312.1988.tb00455.xM. A. Condon, L. E. Gilbert SEX EXPRESSION OF GURANIA AND PSIGURIA (CUCURBITACEAE): NEOTROPICAL VINES THAT CHANGE SEX, American Journal of Botany 75, no.6Part16Part1 (Jun 1988): 875–884.https://doi.org/10.1002/j.1537-2197.1988.tb13511.xJames D. Thomson Effects of variation in inflorescence size and floral rewards on the visitation rates of traplining pollinators ofAralia hispida, Evolutionary Ecology 2, no.11 (Jan 1988): 65–76.https://doi.org/10.1007/BF02071589Conley K. McMullen BREEDING SYSTEMS OF SELECTED GALAPAGOS ISLANDS ANGIOSPERMS, American Journal of Botany 74, no.1111 (Nov 1987): 1694–1705.https://doi.org/10.1002/j.1537-2197.1987.tb08770.xG. E. Muenchow IS DIOECY ASSOCIATED WITH FLESHY FRUIT?, American Journal of Botany 74, no.22 (Feb 1987): 287–293.https://doi.org/10.1002/j.1537-2197.1987.tb08607.xAlina M. Szmant Reproductive ecology of Caribbean reef corals, Coral Reefs 5, no.11 (Aug 1986): 43–53.https://doi.org/10.1007/BF00302170David G. Lloyd, C. J. Webb The avoidance of interference between the presentation of pollen and stigmas in angiosperms I. Dichogamy, New Zealand Journal of Botany 24, no.11 (Jan 1986): 135–162.https://doi.org/10.1080/0028825X.1986.10409725C. J. Webb Protandry, pollination, and self-incompatibility in Discaria toumatou, New Zealand Journal of Botany 23, no.22 (Apr 1985): 331–335.https://doi.org/10.1080/0028825X.1985.10425335Gerhard Gottsberger Floral Ecology Report on the Years 1981(79) to 1985, (Jan 1985): 384–417.https://doi.org/10.1007/978-3-642-45607-7_22Brian Charlesworth Genetic Constraints on the Evolution of Plant Reproductive Systems, (Jan 1985): 155–179.https://doi.org/10.1007/978-3-642-48125-3_11H. E. Connor Breeding systems in New Zealand grasses IX: Sex ratios in dioecious Spinifex sericeus, New Zealand Journal of Botany 22, no.44 (Oct 1984): 569–574.https://doi.org/10.1080/0028825X.1984.10425292 Gregory J. Anderson , and G. Ledyard Stebbins Dioecy Versus Gametophytic Self-Incompatibility: A Test, The American Naturalist 124, no.33 (Oct 2015): 423–428.https://doi.org/10.1086/284283 Herbert G. Baker Some Functions of Dioecy in Seed Plants, The American Naturalist 124, no.22 (Oct 2015): 149–158.https://doi.org/10.1086/284260D. CHARLESWORTH Androdioecy and the evolution of dioecy, Biological Journal of the Linnean Society 22, no.44 (Jan 2008): 333–348.https://doi.org/10.1111/j.1095-8312.1984.tb01683.xElizabeth M. Lord CLEISTOGAMY: A COMPARATIVE STUDY OF INTRASPECIFIC FLORAL VARIATION, (Jan 1984): 451–494.https://doi.org/10.1016/B978-0-12-746620-0.50016-4Mary H. Powlesland Reproductive biology of three species of Melicytus (Violaceae) in New Zealand, New Zealand Journal of Botany 22, no.11 (Jan 1984): 81–94.https://doi.org/10.1080/0028825X.1984.10425235ROBERT WYATT Pollinator–Plant Interactions and the Evolution of Breeding Systems, (Jan 1983): 51–95.https://doi.org/10.1016/B978-0-12-583980-8.50011-9 David G. Lloyd Selection of Combined Versus Separate Sexes in Seed Plants, The American Naturalist 120, no.55 (Oct 2015): 571–585.https://doi.org/10.1086/284014Carlos M. Herrera BREEDING SYSTEMS AND DISPERSAL-RELATED MATERNAL REPRODUCTIVE EFFORT OF SOUTHERN SPANISH BIRD-DISPERSED PLANTS, Evolution 36, no.66 (May 2017): 1299–1314.https://doi.org/10.1111/j.1558-5646.1982.tb05499.x Thomas J. Givnish Outcrossing Versus Ecological Constraints in the Evolution of Dioecy, The American Naturalist 119, no.66 (Oct 2015): 849–865.https://doi.org/10.1086/283959 K. S. Bawa Outcrossing and the Incidence of Dioecism in Island Floras, The American Naturalist 119, no.66 (Oct 2015): 866–871.https://doi.org/10.1086/283960 Mary F. Willson Sexual Selection and Dicliny in Angiosperms, The American Naturalist 119, no.44 (Oct 2015): 579–583.https://doi.org/10.1086/283934James D. Thomson, Spencer C. H. Barrett TEMPORAL VARIATION OF GENDER IN ARALIA HISPIDA VENT. (ARALIACEAE), Evolution 35, no.66 (May 2017): 1094–1107.https://doi.org/10.1111/j.1558-5646.1981.tb04979.xRodrigo Lemes Martins, Tânia Wendt, Rogério Margis, Fabio Rubio Scarano Reproductive Biology, (): 73–94.https://doi.org/10.1007/978-3-540-37243-1_6

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