Title: Asexual Reproduction: A Further Consideration
Abstract: Previous articleNext article No AccessLetters to the EditorsAsexual Reproduction: A Further ConsiderationRobert Edward CookRobert Edward CookPDFPDF PLUS Add to favoritesDownload CitationTrack CitationsPermissionsReprints Share onFacebookTwitterLinkedInRedditEmail SectionsMoreDetailsFiguresReferencesCited by The American Naturalist Volume 113, Number 5May, 1979 Published for The American Society of Naturalists Article DOIhttps://doi.org/10.1086/283435 Views: 123Total views on this site Citations: 94Citations are reported from Crossref Copyright 1979 The University of ChicagoPDF download Crossref reports the following articles citing this article:Maximilian Schweinsberg, Fabian Gösser, Ralph Tollrian The history, biological relevance, and potential applications for polyp bailout in corals, Ecology and Evolution 76 (Jun 2021).https://doi.org/10.1002/ece3.7740María Dolores Rosas Barrera, Jordan Golubov, Irene Pisanty, Maria C. 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Dalrymple, Joanna M. Buswell, Angela T. Moles Asexual plants change just as often and just as fast as do sexual plants when introduced to a new range, Oikos 124, no.22 (Jul 2014): 196–205.https://doi.org/10.1111/oik.01582Shin Fukui, Kiwako S. Araki, Sergio R. Roiloa Spatial Niche Facilitates Clonal Reproduction in Seed Plants under Temporal Disturbance, PLoS ONE 9, no.1212 (Dec 2014): e116111.https://doi.org/10.1371/journal.pone.0116111Naruya Saitou Neutral Evolution, (Nov 2013): 89–124.https://doi.org/10.1007/978-1-4471-5304-7_4Ellen Clarke Plant individuality: a solution to the demographer's dilemma, Biology & Philosophy 27, no.33 (Mar 2012): 321–361.https://doi.org/10.1007/s10539-012-9309-3Charles L. Argue Tribe Calypsoeae, (Aug 2011): 105–139.https://doi.org/10.1007/978-1-4614-0622-8_6A. Gibert, L. 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Taylor, Michael Arnold, Noland H. Martin THE GENETIC ARCHITECTURE OF REPRODUCTIVE ISOLATION IN LOUISIANA IRISES: HYBRID FITNESS IN NATURE, Evolution 63, no.1010 (Oct 2009): 2581–2594.https://doi.org/10.1111/j.1558-5646.2009.00742.xEva Gonzales, J. L. Hamrick, Peter E. Smouse Comparison of clonal diversity in mountain and Piedmont populations of Trillium cuneatum (Melanthiaceae‐Trilliaceae), a forest understory species, American Journal of Botany 95, no.1010 (Oct 2008): 1254–1261.https://doi.org/10.3732/ajb.2007159Lonnie W. Aarssen Death without sex—the 'problem of the small' and selection for reproductive economy in flowering plants, Evolutionary Ecology 22, no.33 (May 2007): 279–298.https://doi.org/10.1007/s10682-007-9170-zM. J. M. Hay, C. K. Kelly Have clonal plant biologists got it wrong? The case for changing the emphasis to disintegration, Evolutionary Ecology 22, no.33 (Jul 2007): 461–465.https://doi.org/10.1007/s10682-007-9193-5Flávia Freitas Coelho, Christina Capelo, José Eugênio C. Figueira Seedlings and ramets recruitment in two rhizomatous species of Rupestrian grasslands: Leiothrix curvifolia var. lanuginosa and Leiothrix crassifolia (Eriocaulaceae), Flora - Morphology, Distribution, Functional Ecology of Plants 203, no.22 (Mar 2008): 152–161.https://doi.org/10.1016/j.flora.2007.02.005Yufen Zhang, Dayong Zhang Asexual and sexual reproductive strategies in clonal plants, Frontiers of Biology in China 2, no.33 (Jul 2007): 256–262.https://doi.org/10.1007/s11515-007-0036-0R. Elahi, P. J. Edmunds Consequences of fission in the coral Siderastrea siderea: growth rates of small colonies and clonal input to population structure, Coral Reefs 26, no.22 (Feb 2007): 271–276.https://doi.org/10.1007/s00338-006-0190-xJ. T. Wright, A. R. Davis DEMOGRAPHIC FEEDBACK BETWEEN CLONAL GROWTH AND FRAGMENTATION IN AN INVASIVE SEAWEED, Ecology 87, no.77 (Jul 2006): 1744–1754.https://doi.org/10.1890/0012-9658(2006)87[1744:DFBCGA]2.0.CO;2Inoue Mizuki, Kiyoshi Ishida, Kihachiro Kikuzawa Sexual and vegetative reproduction in the aboveground part of a dioecious clonal plant, Dioscorea japonica (Dioscoreaceae), Ecological Research 20, no.44 (Feb 2005): 387–393.https://doi.org/10.1007/s11284-005-0036-yChristopher T. Frye Persistence of Allozyme and Clonal Diversity in an Insular Population of Cleistes bifaria (Fern.) Catling and Gregg (Orchidaceae) in Wilkes County, North Carolina, Southeastern Naturalist 4, no.22 (Jun 2005): 287–302.https://doi.org/10.1656/1528-7092(2005)004[0287:POAACD]2.0.CO;2Cecilia Alfonso-Corrado, Rocío Esteban-Jiménez, Ricardo Clark-Tapia, Daniel Piñero, Jorge E. Campos, Ana Mendoza Clonal and genetic structure of two Mexican oaks: Quercus eduardii and Quercus potosina (Fagaceae), Evolutionary Ecology 18, no.5-65-6 (May 2005): 585–599.https://doi.org/10.1007/s10682-004-5145-5Josef F. Stuefer, Sara Gómez, Tamara van Mölken Clonal integration beyond resource sharing: implications for defence signalling and disease transmission in clonal plant networks, Evolutionary Ecology 18, no.5-65-6 (May 2005): 647–667.https://doi.org/10.1007/s10682-004-5148-2Satoshi NANAMI, Hideyuki KAWAGUCHI, Ryunosuke TATENO, Changhua LI, Shigeo KATAGIRI Sprouting traits and population structure of co-occurring Castanopsis species in an evergreen broad-leaved forest in southern China, Ecological Research 19, no.33 (May 2004): 341–348.https://doi.org/10.1111/j.1440-1703.2004.00643.xTamara M. McGovern Plastic reproductive strategies in a clonal marine invertebrate, Proceedings of the Royal Society of London. Series B: Biological Sciences 270, no.15321532 (Dec 2003): 2517–2522.https://doi.org/10.1098/rspb.2003.2529Jean J. Pan, Keith Clay Infection by the systemic fungus Epichloë glyceriae alters clonal growth of its grass host, Glyceria striata, Proceedings of the Royal Society of London. Series B: Biological Sciences 270, no.15241524 (Aug 2003): 1585–1591.https://doi.org/10.1098/rspb.2003.2428A. Hammerli, T. B. H. Reusch Inbreeding depression influences genet size distribution in a marine angiosperm, Molecular Ecology 12, no.33 (Mar 2003): 619–629.https://doi.org/10.1046/j.1365-294X.2003.01766.xTrevor C Lantz, Joseph A Antos Clonal expansion in the deciduous understory shrub, devil's club ( Oplopanax horridus ; Araliaceae), Canadian Journal of Botany 80, no.1010 (Oct 2002): 1052–1062.https://doi.org/10.1139/b02-095J. F. Stuefer, J.B. Van Hulzen, H. J. During A genotypic trade‐off between the number and size of clonal offspring in the stoloniferous herb Potentilla reptans, Journal of Evolutionary Biology 15, no.55 (Aug 2002): 880–884.https://doi.org/10.1046/j.1420-9101.2002.00435.xJean J. Pan, Keith Clay Infection by the systemic fungus Epichloë glyceriae and clonal growth of its host grass Glyceria striata, Oikos 98, no.11 (Jul 2002): 37–46.https://doi.org/10.1034/j.1600-0706.2002.980104.xJennifer A. Schweitzer, Gregory D. Martinsen, Thomas G. Whitham Cottonwood hybrids gain fitness traits of both parents: a mechanism for theirlong‐term persistence?, American Journal of Botany 89, no.66 (Jun 2002): 981–990.https://doi.org/10.3732/ajb.89.6.981Machiko Kimura, Herwint Simbolon Allometry and life history of a forest understory palm Pinanga coronata (Arecaceae) on Mount Halimun, West Java, Ecological Research 17, no.33 (Jul 2002): 323–338.https://doi.org/10.1046/j.1440-1703.2002.00492.xJean J. Pan, Jason S. Price Fitness and evolution in clonal plants: the impact of clonal growth, (Jan 2002): 361–378.https://doi.org/10.1007/978-94-017-1345-0_20Nadia Barsoum Relative contributions of sexual and asexual regeneration strategies in Populus nigra and Salix alba during the first years of establishment on a braided gravel bed river, (Jan 2002): 33–57.https://doi.org/10.1007/978-94-017-1345-0_3Tamara M. McGovern SEX-RATIO BIAS AND CLONAL REPRODUCTION IN THE BRITTLE STAR OPHIACTIS SAVIGNYI, Evolution 56, no.33 (Jan 2002): 511.https://doi.org/10.1554/0014-3820(2002)056[0511:SRBACR]2.0.CO;2Colleen K. Kelly, Daniel Harris, Ruben Perez-Ishiwara Is breaking up hard to do? Breakage, growth, and survival in the parasitic clonal plant Cuscuta corymbosa (Convolvulaceae), American Journal of Botany 88, no.88 (Aug 2001): 1458–1468.https://doi.org/10.2307/3558454Nadia Barsoum Relative contributions of sexual and asexual regeneration strategies in Populus nigra and Salix alba during the first years of establishment on a braided gravel bed river, Evolutionary Ecology 15, no.4-64-6 (Jul 2001): 255–279.https://doi.org/10.1023/A:1016028730129Jean J. Pan, Jason S. Price Fitness and evolution in clonal plants: the impact of clonal growth, Evolutionary Ecology 15, no.4-64-6 (Jul 2001): 583–600.https://doi.org/10.1023/A:1016065705539Jason E. Tanner THE INFLUENCE OF CLONALITY ON DEMOGRAPHY: PATTERNS IN EXPECTED LONGEVITY AND SURVIVORSHIP, Ecology 82, no.77 (Jul 2001): 1971–1981.https://doi.org/10.1890/0012-9658(2001)082[1971:TIOCOD]2.0.CO;2Dushyantha K. Wijesinghe, Dennis F. Whigham Nutrient foraging in woodland herbs: a comparison of three species of Uvularia (Liliaceae) with contrasting belowground morphologies, American Journal of Botany 88, no.66 (Jun 2001): 1071–1079.https://doi.org/10.2307/2657090María C. Mandujano, Carlos Montaña, Miguel Franco, Jordan Golubov, Arturo Flores-Martínez INTEGRATION OF DEMOGRAPHIC ANNUAL VARIABILITY IN A CLONAL DESERT CACTUS, Ecology 82, no.22 (Feb 2001): 344–359.https://doi.org/10.1890/0012-9658(2001)082[0344:IODAVI]2.0.CO;2Ana C. Villegas Spatial and Temporal Variability in Clonal Reproduction of Aechmea magdalenae, a Tropical Understory Herb1, BIOTROPICA 33, no.11 (Jan 2001): 48.https://doi.org/10.1646/0006-3606(2001)033[0048:SATVIC]2.0.CO;2Deborah L Rogers Genotypic diversity and clone size in old-growth populations of coast redwood ( Sequoia sempervirens ), Canadian Journal of Botany 78, no.1111 (Nov 2000): 1408–1419.https://doi.org/10.1139/b00-114Marie-Josée Laberge, Serge Payette, Jean Bousquet Life span and biomass allocation of stunted black spruce clones in the subarctic environment, Journal of Ecology 88, no.44 (Aug 2000): 584–593.https://doi.org/10.1046/j.1365-2745.2000.00471.x Freeland, Noble, Okamura Genetic consequences of the metapopulation biology of a facultatively sexual freshwater invertebrate, Journal of Evolutionary Biology 13, no.33 (May 2000): 383–395.https://doi.org/10.1046/j.1420-9101.2000.00192.xYUKO HARADA Short- vs. Long-range Disperser: the Evolutionarily Stable Allocation in a Lattice-Structured Habitat, Journal of Theoretical Biology 201, no.33 (Dec 1999): 171–187.https://doi.org/10.1006/jtbi.1999.1022Shea N. Gardner, Marc Mangel MODELING INVESTMENTS IN SEEDS, CLONAL OFFSPRING, AND TRANSLOCATION IN A CLONAL PLANT, Ecology 80, no.44 (Jun 1999): 1202–1220.https://doi.org/10.1890/0012-9658(1999)080[1202:MIISCO]2.0.CO;2Jun-Ichirou Suzuki, Josef Stuefer On the ecological and evolutionary significance of storage in clonal plants, Plant Species Biology 14, no.11 (Apr 1999): 11–17.https://doi.org/10.1046/j.1442-1984.1999.00002.xL.D Smith, T.P Hughes An experimental assessment of survival, re-attachment and fecundity of coral fragments, Journal of Experimental Marine Biology and Ecology 235, no.11 (Mar 1999): 147–164.https://doi.org/10.1016/S0022-0981(98)00178-6Hiroshi Kudoh, Hiroyuki Shibaike, Hideki Takasu, Dennis F. Whigham, Shoichi Kawano Genet structure and determinants of clonal structure in a temperate deciduous woodland herb, Uvularia perfoliata, Journal of Ecology 87, no.22 (Mar 1999): 244–257.https://doi.org/10.1046/j.1365-2745.1999.00355.xL. David Humphrey, David A. Pyke Demographic and growth responses of a guerrilla and a phalanx perennial grass in competitive mixtures, Journal of Ecology 86, no.55 (Oct 1998): 854–865.https://doi.org/10.1046/j.1365-2745.1998.8650854.xJohn H. Andrews BACTERIA AS MODULAR ORGANISMS, Annual Review of Microbiology 52, no.11 (Oct 1998): 105–126.https://doi.org/10.1146/annurev.micro.52.1.105 Shea N. Gardner and Marc Mangel When Can a Clonal Organism Escape Senescence? Gardner & Mangel, The American Naturalist 150, no.44 (Jul 2015): 462–490.https://doi.org/10.1086/286076Michael J. Hutchings, Roy Turkington, Elena Klein, Peter Carey Morphological plasticity in Trifolium repens L.: the effects of clone genotype, soil nutrient level, and the genotype of conspecific neighbours, Canadian Journal of Botany 75, no.88 (Aug 1997): 1382–1393.https://doi.org/10.1139/b97-852Elizabeth A. C. Price, Michael J. Hutchings, Christopher Marshall Causes and consequences of sectoriality in the clonal herb Glechoma hederacea, Vegetatio 127, no.11 (Nov 1996): 41–54.https://doi.org/10.1007/BF00054846LAURA UOTILA, JUKKA JOKEL Variation in reproductive characteristics of colonies of the freshwater bryozoan Cristatella mucedo, Freshwater Biology 34, no.33 (May 2006): 513–522.https://doi.org/10.1111/j.1365-2427.1995.tb00909.xJuan A. Amat Effects of wintering greylag geese Anser anser on their Scirpus food plants, Ecography 18, no.22 (Jun 1995): 155–163.https://doi.org/10.1111/j.1600-0587.1995.tb00336.xYuko Harada, Yoh Iwasa Lattice population dynamics for plants with dispersing seeds and Vegetative propagation, Researches on Population Ecology 36, no.22 (Dec 1994): 237–249.https://doi.org/10.1007/BF02514940Petr Zákravský, Zdenka Hroudová The effect of submergence on tuber production and dormancy in two subspecies ofBolboschoenus maritimus, Folia Geobotanica et Phytotaxonomica 29, no.22 (Jun 1994): 217–226.https://doi.org/10.1007/BF02803796Ove Eriksson Dynamics of genets in clonal plants, Trends in Ecology & Evolution 8, no.99 (Sep 1993): 313–316.https://doi.org/10.1016/0169-5347(93)90237-JGordon A. Fox Annual plant life histories and the paradigm of resource allocation, Evolutionary Ecology 6, no.66 (Nov 1992): 482–499.https://doi.org/10.1007/BF02270693Dennis E. Jelinski, W. M. Cheliak GENETIC DIVERSITY AND SPATIAL SUBDIVISION OF POPULUS TREMULOIDES (SALICACEAE) IN A HETEROGENEOUS LANDSCAPE, American Journal of Botany 79, no.77 (Jul 1992): 728–736.https://doi.org/10.1002/j.1537-2197.1992.tb13647.xFilip Ridder, Andre A. Dhondt The demography of a clonal herbaceous perennial plant, the longleaved sundew Drosera intermedia, in different heathland habitats, Ecography 15, no.22 (Apr 1992): 129–143.https://doi.org/10.1111/j.1600-0587.1992.tb00016.x Park S. Nobel Annual Variations in Flowering Percentage, Seedling Establishment, and Ramet Production for a Desert Perennial, International Journal of Plant Sciences 153, no.11 (Oct 2015): 102–107.https://doi.org/10.1086/297011Warren G. Abrahamson, Stephen S. Anderson, Kenneth D. McCrea CLONAL INTEGRATION: NUTRIENT SHARING BETWEEN SISTER RAMETS OF SOLIDAGO ALTISSIMA (COMPOSITAE), American Journal of Botany 78, no.1111 (Nov 1991): 1508–1514.https://doi.org/10.1002/j.1537-2197.1991.tb11430.xLaura J. Stocker, Antony J. Underwood The relationship between the presence of neighbours and rates of sexual and asexual reproduction in a colonial invertebrate, Journal of Experimental Marine Biology and Ecology 149, no.22 (Jul 1991): 191–205.https://doi.org/10.1016/0022-0981(91)90045-XC. Drew Harvell, Hal Caswell, Paul Simpson Density effects in a colonial monoculture: experimental studies with a marine bryozoan (Membranipora membranacea L.), Oecologia 82, no.22 (Feb 1990): 227–237.https://doi.org/10.1007/BF00323539KRYSTYNA M. URBANSKA Biology of Asexually Reproducing Plants, (Jan 1990): 273–292.https://doi.org/10.1016/B978-0-12-402960-6.50021-4Bobby D. Bennett, James B. Grace SHADE TOLERANCE AND ITS EFFECT ON THE SEGREGATION OF TWO SPECIES OF LOUISIANA IRIS AND THEIR HYBRIDS, American Journal of Botany 77, no.11 (Jan 1990): 100–107.https://doi.org/10.1002/j.1537-2197.1990.tb13532.xOla Inghe Genet and ramet survivorship under different mortality regimes—A cellular automata model, Journal of Theoretical Biology 138, no.22 (May 1989): 257–270.https://doi.org/10.1016/S0022-5193(89)80142-0B. E. Olson, J. H. Richards Annual replacement of the tillers of Agropyron desertorum following grazing, Oecologia 76, no.11 (Jun 1988): 1–6.https://doi.org/10.1007/BF00379592B. E. Olson, J. H. Richards Spatial arrangement of tiller replacement in Agropyron desertorum following grazing, Oecologia 76, no.11 (Jun 1988): 7–10.https://doi.org/10.1007/BF00379593Robert E. Cook GROWTH IN MEDEOLA VIRGINIANA CLONES I. FIELD OBSERVATIONS, American Journal of Botany 75, no.55 (May 1988): 725–731.https://doi.org/10.1002/j.1537-2197.1988.tb13493.xH.J. During, B.F. van Tooren Recent developments in bryophyte population ecology, Trends in Ecology & Evolution 2, no.44 (Apr 1987): 89–93.https://doi.org/10.1016/0169-5347(87)90164-9James A. Reinartz, James W. Popp STRUCTURE OF CLONES OF NORTHERN PRICKLY ASH (XANTHOXYLUM AMERICANUM), American Journal of Botany 74, no.33 (Mar 1987): 415–428.https://doi.org/10.1002/j.1537-2197.1987.tb08623.x Deborah O. Raphael , and Park S. Nobel Growth and Survivorship of Ramets and Seedlings of Agave deserti: Influences of Parent-Ramet Connections, Botanical Gazette 147, no.11 (Oct 2015): 78–83.https://doi.org/10.1086/337571Kenneth D. McCrea, Warren G. Abrahamson Evolutionary impacts of the goldenrod ball gallmaker on Solidago altissima clones, Oecologia 68, no.11 (Dec 1985): 20–22.https://doi.org/10.1007/BF00379467 Joseph A. Antos , and Donald B. Zobel Ecological Implications of Belowground Morphology of Nine Coniferous Forest Herbs, Botanical Gazette 145, no.44 (Oct 2015): 508–517.https://doi.org/10.1086/337486 Terence P. Hughes Population Dynamics Based on Individual Size Rather than Age: A General Model with a Reef Coral Example, The American Naturalist 123, no.66 (Oct 2015): 778–795.https://doi.org/10.1086/284239Robert A. Armstrong On the quantitative theory of reproductive effort in clonal plants: Refinements of theory, with evidence from goldenrods and mayapples, Oecologia 63, no.33 (Jan 1984): 410–417.https://doi.org/10.1007/BF00390674R. N. HUGHES Evolutionary ecology of colonial reef-organisms, with particular reference to corals, Biological Journal of the Linnean Society 20, no.11 (Jan 2008): 39–58.https://doi.org/10.1111/j.1095-8312.1983.tb01588.xJ. B. C. Jackson Biological Determinants of Present and Past Sessile Animal Distributions, (Jan 1983): 39–120.https://doi.org/10.1007/978-1-4757-0740-3_2P. L. Jokiel, W. H. Hildemann, C. H. Bigger Frequency of intercolony graft acceptance or rejection as a measure of population structure in the sponge Callyspongia diffusa, Marine Biology 71, no.22 (Jan 1982): 135–139.https://doi.org/10.1007/BF00394621 Mark Westoby How Diversified Seed Germination Behavior is Selected, The American Naturalist 118, no.66 (Oct 2015): 882–885.https://doi.org/10.1086/283880D. A. Thompson, A. J. Beattie DENSITY‐MEDIATED SEED AND STOLON PRODUCTION IN VIOLA (VIOLACEAE), American Journal of Botany 68, no.33 (Mar 1981): 383–388.https://doi.org/10.1002/j.1537-2197.1981.tb06375.xBarbara L. Thorne Genetic consequences of variation in sib maturation schedules, Acta Biotheoretica 30, no.44 (Jan 1981): 219–227.https://doi.org/10.1007/BF00051768Brian Charlesworth The cost of meiosis with alternation of sexual and asexual generations, Journal of Theoretical Biology 87, no.33 (Dec 1980): 517–528.https://doi.org/10.1016/0022-5193(80)90233-7Charles M. Wahle Detection, Pursuit, and Overgrowth of Tropical Gorgonians by Milleporid Hydrocorals: Perseus and Medusa Revisited, Science 209, no.44574457 (Aug 1980): 689–691.https://doi.org/10.1126/science.209.4457.689
Publication Year: 1979
Publication Date: 1979-05-01
Language: en
Type: article
Indexed In: ['crossref']
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Cited By Count: 166
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