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Speciation and Morphological Evolution in Rheophytes

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Evolution and Diversification of Land Plants

Abstract

It is widely accepted that species are defined to be reproductively isolated groups within which natural populations interbreed [1,2]. According to this biological species concept, if reproductive isolation is established among populations, valid species could be produced. The implication is that speciation need not be accompanied by any detectable morphological changes [3]. In plants with limited movement, however, speciation is sometimes associated with distinct morphological changes, which enable plants to invade new ecological niches. The mode of speciation may hold in the case for the evolution of rheophytes.

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References

  1. Mayr E (1970) Populations, species, and evolution. Harvard University Press, Cambridge

    Google Scholar 

  2. Grant V (1981) Plant speciation, 2nd edn. Columbia University Press, New York

    Google Scholar 

  3. Stanley SM (1982) Speciation and the fossil record. In: Barigozzi C (ed) Mechanisms of speciation. Liss, New York, pp 41–49

    Google Scholar 

  4. Van Steenis CGGJ (1981) Rheophytes of the world. Sijthoff & Noordhoff, Alphen aan den Rijin

    Book  Google Scholar 

  5. Kato M, Imaichi R (1992) Leaf anatomy of tropical fern rheophytes, with its evolutionary and ecological implications. Can J Bot 70:165–174

    Article  Google Scholar 

  6. Metcalfe CR, Chalk L (1950) Anatomy of the dicotyledons, vol 2. Clarendon, Oxford

    Google Scholar 

  7. Nobel SP, Zaragoza LJ, Smith WK (1975) Relation between mesophyll surface area, photosynthetic rate, and illumination level during development for leaves of Plectranthus parviflorus Henckel. Plant Physiol (Bethesda) 55:1067–1070

    Article  CAS  Google Scholar 

  8. Koike T (1988) Leaf structure and photosynthetic performance as related to the forest succession of deciduous broad-leaved trees. Plant Species Biol 3:77–87

    Article  Google Scholar 

  9. Juniper BE, Jeffree CE (1983) Plant surfaces. Arnold, London

    Google Scholar 

  10. Hiyama T, Imaichi R, Kato M (1992) Comparative development of gametophytes of Osmunda lancea and O. japonica (Osmundaceae): adaptation of rheophilous fern gametophyte. Bot Mag Tokyo 105:215–225

    Article  Google Scholar 

  11. Imaichi R, Kato M (1992) Comparative leaf development of Osmunda lancea and O. japonica (Osmundaceae): heterochronic origin of rheophytic stenophylly. Bot Mag Tokyo 105:199–213

    Article  Google Scholar 

  12. Imaichi R, Kato M (1993) Comparative leaf morphology of young sporophytes of rheophytic Osmunda lancea and dryland O. japonica. J Plant Res 106:37–45

    Article  Google Scholar 

  13. Gould SJ (1977) Ontogeny and phylogeny. Harvard University Press, Cambridge

    Google Scholar 

  14. Alberch P, Gould SJ, Oster GF, Wake DB (1979) Size and shape in ontogeny and phylogeny. Paleobiology 5:296–317

    Google Scholar 

  15. Hilu KW (1983) The role of single-gene mutations in the evolution of flowering plants. Evol Biol 16:97–128

    Article  Google Scholar 

  16. Gottlieb LD (1984) Genetics and morphological evolution in plants. Am Nat 123:681–709

    Article  Google Scholar 

  17. Ambros V, Horvitz HR (1984) Heterochronic mutants of the nematode Caenorhabditis elegans. Science 226:409–416

    Article  PubMed  CAS  Google Scholar 

  18. Ambros V, Fixsen W (1987) Cell lineage variation among nematodes. In: Raff RA, Raff EC (eds) Development as an evolutionary process. Liss, New York, pp 139–159

    Google Scholar 

  19. Kato M, Imaichi R (1992) A broad-leaved variant of the fern rheophyte, Tectaria lobbii. Int J Plant Sci 153:212–216

    Article  Google Scholar 

  20. Usukura M, Imaichi R, Kato M (1994) Leaf morphology of a facultative rheophyte, Farfugium japonicum var. luchuense (Compositae). J Plant Res 107:263–267

    Article  Google Scholar 

  21. Futuyma DJ (1986) Evolutionary biology, 2nd edn. Sinauer, Sunderland

    Google Scholar 

  22. Eldredge N, Gould SJ (1972) Punctuated equilibria: an alternative to phyletic gradualism. In: Schopf TJM (ed) Models in paleobiology. Freeman, San Francisco, pp 82–115

    Google Scholar 

  23. Stebbins GL, Ayala FJ (1981) Is a new evolutionary synthesis necessary? Science 213:967–971

    Article  PubMed  CAS  Google Scholar 

  24. Ayala FJ (1982) Gradualism versus punctualism in speciation: reproductive isolation, morphology, genetics. In: Barigozzi C (ed) Mechanisms of speciation. Liss, New York, pp 51–66

    Google Scholar 

  25. Jaynes RA (1981) Inheritance of ornamental traits in mountain laurel, Kalmia latifolia. J Hered 72:245–248

    Google Scholar 

  26. Bassett MJ (1981) Inheritance of a lanceolate leaf mutation in the common bean. J Hered 72:431–432

    Google Scholar 

  27. Shimura Y (1972) Study of reproduction of Osmunda × intermedia Sugimoto (in Japanese with English summary). J Geobot 20:38–42

    Google Scholar 

  28. Shimura Y, Matsumoto S (1977) On the chromosome association in meiosis of Osmunda × intermedia. J Jpn Bot 52:377–378

    Google Scholar 

  29. Tsuge T, Tsukaya H, Uchimiya H (1996) Two independent and polarized processes of cell elongation regulate leaf blade expansion in Arabidopsis thaliana (L.) Heynh. Development (Camb) 122:1589–1600

    CAS  Google Scholar 

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© 1997 Springer-Verlag Tokyo

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Imaichi, R., Kato, M. (1997). Speciation and Morphological Evolution in Rheophytes. In: Iwatsuki, K., Raven, P.H. (eds) Evolution and Diversification of Land Plants. Springer, Tokyo. https://doi.org/10.1007/978-4-431-65918-1_15

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  • DOI: https://doi.org/10.1007/978-4-431-65918-1_15

  • Publisher Name: Springer, Tokyo

  • Print ISBN: 978-4-431-65920-4

  • Online ISBN: 978-4-431-65918-1

  • eBook Packages: Springer Book Archive

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