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Histopathology of Seed-Borne Infections - Applied Research Center ...

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Reproductive Structures and <strong>Seed</strong> Formation 41through the synergid, and lack <strong>of</strong> evidence that the sperm cytoplasm enters the eggor the central cell, are recorded during pollination and fertilization.The development <strong>of</strong> the endosperm may be nuclear, cellular, or helobial.Endosperm haustoria are found in several taxa <strong>of</strong> angiosperms. Available informationshows absence <strong>of</strong> plasmodesmatal connections in the embryo sac wall and thesurrounding tissue. Development <strong>of</strong> protuberances on the internal surface and themicroinvagination <strong>of</strong> plasmalemma, similar to those <strong>of</strong> transfer cells, are observed.This indicates that the transfer <strong>of</strong> nutrients from the maternal tissues to the newsporophyte including the endosperm takes place apoplastically.The development <strong>of</strong> the proembryo is similar in dicotyledons and monocotyledons.Differences develop during the organization <strong>of</strong> various parts <strong>of</strong> the embryo.The proembryo gets its nutrition through its basal suspensor cells, which developwall ingrowths. During the later stages nutrition is obtained from the endosperm.Changes take place in the nucellus, chalaza, and integument during seed development.Integuments undergo differentiation, absorption <strong>of</strong> cell layers, thickening<strong>of</strong> cell walls, and deposition <strong>of</strong> pigmented material and crystals etc. One or morelayers <strong>of</strong> the seed coat develop characteristic thickenings, forming the main mechanicallayer. The seed coat is testal if the main mechanical layer is formed in the outerintegument and tegmic if it differentiates in the inner integument <strong>of</strong> a bitegmic ovule.Each type has several subtypes. The development and structure <strong>of</strong> the seed coat isfairly constant in a family.REFERENCESAgthe, C. 1951. Über die physiologische Herkunft des Pflanzen-nektars. Ber. Schweiz. Bot.Ges. 61: 240–277.Anderson, M.A., Lee, M., Heath, R.L., Nielson, K.J., Craik, D.J., Guest, D.J., and Clarke,A.E. 1996. Defence-related molecules in the pistil <strong>of</strong> Nicotiana alata. Plant Reproduction.14th International Congress <strong>of</strong> Sexual Plant Reproduction, Lorne (nearMelbourne, Australia), Abstract, p. 1.Arber, A. 1937. The interpretation <strong>of</strong> the flower: a study <strong>of</strong> some aspects <strong>of</strong> morphologicalthought. Biol. Rev. 12: 157–184.Atkinson, A.H., Heath, R.L., Simpson, R.J., Clarke, A.E., and Anderson, M.A. 1993. Proteinaseinhibitors in Nicotiana alata stigmas are derived from a precursor protein whichis processed into five homologous inhibitors. Plant Cell 5: 203–213.Baker, D.M. and Mebrahtu, T. 1990. Scanning electron microscopy examination <strong>of</strong> soybeanhilum development. Am. J. Bot. 68: 544–550.Bhatnagar, S.P. and Johri, B.M. 1972. Development <strong>of</strong> angiosperm seed. In <strong>Seed</strong> Biology.Kozlowski, T.T., Ed. Academic Press, New York, Vol. 1, pp. 77–149.Bocquet, G. 1959. The campylotropous ovule. Phytomorphology 9: 222–227.Boesewinkel, F.D. 1980. Development <strong>of</strong> ovule and testa <strong>of</strong> Linum usitatissimum. L. ActaBot. Neerl. 29: 17–32.Bor, J. and Bouman, F. 1974. Development <strong>of</strong> ovule and integuments in Euphorbia milli andCodiaeum variegatum. Phytomorphology 24: 280–296.Bouman, F. 1984. The Ovule. In Embryology <strong>of</strong> Angiosperms. Johri, B.M., Ed. Springer-Verlag, Berlin, pp. 123–157.

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