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A route for the passage of substances through the developing pteridophyte exine

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Summary

The developing exine ofLycopodium gnidioides is traversed from the outer to the inner surface by a series of anastomosing channels filled or lined with fibrillar glycoprotein. When living sporangia are incubated in colloidal iron, particles of ferric iron can be detected in the exine channels, the intine and the spore cytoplasm, and some iron is retained by the surface coatings on the spore. Although there is some diffuse iron staining of the exine between the channels, the main concentration of particles is associated with these structures. This, together with the fact that the proximal lasurae of the spore are closed during development, is taken as evidence that the iron has passed from the locular fluid to the surface of the protoplast principally by way of the exine channels. Results obtained from fixation in a glutaraldehyde-lanthanum nitrate mixture support this interpretation. While the exine channels are in existence, therefore, the spore protoplast is in open communication with the locular environment. The study provides no evidence to suggest that the iron which entered the spore cytoplasm did so by endocytosis. It is possible that iron altered the permeability of the plasma membrane by damaging its structure; entry of iron to the cytoplasm being effected through the damaged membrane.

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References

  • Bennett, H. S., 1969 a: The cell surface: components and configurations. In: Handbook of molecular cytology, pp. 1261–1293 (A. Lima-de-Faria, ed.). Amsterdam-London: North Holland Publishing Company.

    Google Scholar 

  • — 1969 b: The cell surface: movements and recombinations. In: Handbook of molecular cytology, pp. 1294–1319 (A. Lima-de-Faria, ed.). Amsterdam-London: North Holland Publishing Company.

    Google Scholar 

  • Christensen, J. E., andH. T. Horner, Jr., 1974: Pollen pore development and its spatial orientation during microsporogenesis in the grassSorghum bicolor. Amer. J. Bot.61, 604–623.

    Google Scholar 

  • — — andN. R. Lersten, 1972: Pollen wall and tapetal orbicular wall development inSorghum bicolor (Gramineae). Amer. J. Bot.59, 43–58.

    Google Scholar 

  • Heslop-Harrison, J., 1975: The physiology of the pollen grain surface. Proc. roy. Soc. (Lond.) B190, 275–299.

    Google Scholar 

  • —,Y. Heslop-Harrison, R. B. Knox, andB. Howlett, 1973: Pollen-wall proteins: “gametophytic” and “sporophytic” fractions in the pollen walls of theMalvaceae. Ann. Bot.37, 403–412.

    Google Scholar 

  • Howlett, B. J., R. B. Knox, andJ. Heslop-Harrison, 1973: Pollen-wall proteins: release of the allergen Antigen E from intine and exine sites in pollen grains of ragweed andCosmos. J. Cell Sci.13, 603–619.

    Google Scholar 

  • Ito, S., 1974: Form and function of the glycocalyx on free cell surfaces. Phil. Trans. (Lond.)B 268, 55–66.

    Google Scholar 

  • Knox, R. B., 1971: Pollen-wall proteins: localization, enzymic and antigenic activity during development inGladiolus (Iridaceae). J. Cell Sci.9, 209–237.

    Google Scholar 

  • — andJ. Heslop-Harrison, 1970: Pollen-wall proteins: localization and enzymic activity. J. Cell Sci.6, 1–27.

    Google Scholar 

  • - - and Y.Heslop-Harrison, 1975: Pollen-wall proteins: localization and characterization of gametophytic and sporophytic fractions. In: The biology of the male gamete, pp. 177–187 (J. G.Duckett and P. A.Racey, eds.). Suppl.1, Biol. J. Linn. Soc. 7.

  • Pettitt, J. M., 1970: Heterospory and the origin of the seed habit. Biol. Rev.45, 401–415.

    Google Scholar 

  • —, 1971: Some ultrastructural aspects of sporoderm formation in pteridophytes. In: Pollen and spore morphology/plant taxonomy. IV. Pteridophyta, pp. 227–251 (G. Erdtman andP. Sorsa, eds.). Stockholm: Almqvist and Wiksell.

    Google Scholar 

  • —, 1974: Developmental mechanisms in heterospory. II. Evidence for pinocytosis in the microspores ofSelaginella. Bot. J. Linn. Soc.69, 79–87.

    Google Scholar 

  • — andA. C. Jermy, 1974: The surface coats on spores. Biol. J. Linn. Soc.6, 245–257.

    Google Scholar 

  • Reynolds, E. S., 1963: The use of lead citrate at a high pH as an electron opaque stain in electron microscopy. J. Cell Biol.17, 208–212.

    Google Scholar 

  • Revel, J. P., andM. J. Karnovsky, 1967: Hexagonal arrays of subunits in intercellular junctions of the mouse heart and liver. J. Cell Biol.33, C 7–12.

    Google Scholar 

  • Rowley, J. R., 1971 a: Resolution of channels in the exine by translocation of colloidal iron (C. J.Arceneaux, ed.). 29th Ann. Proc. E.M. Soc. Amer. Boston Mass.

  • — 1971b: Implications on the nature of sporopollenin based upon pollen development. In: Sporopollenin, pp. 175–218 (J. Brooks, P. R. Grant, M. D. Muir, P. van Gijzel, andG. Shaw, eds.). London: Academic Press.

    Google Scholar 

  • — 1973: Formation of pollen exine bacules and microchannels on a glycocalyx. Grana13, 129–138.

    Google Scholar 

  • — 1975: The permeability of the pollen grain wall to exogenous protein tracers. J. Ultrastruct. Res.50, 394.

    Google Scholar 

  • Rowley, J. R., andA. Dunbar, 1970: Transfer of colloidal iron from sporophyte to gametophyte. Pollen Spores12, 305–328.

    Google Scholar 

  • — andJ. J. Flynn, 1971: Migration of lanthanum through the pollen wall. Cytobiologie3, 1–12.

    Google Scholar 

  • Spurr, A. R., 1969: A low-viscosity epoxy resin embedding medium for electron microscopy. J. Ultrastruct. Res.26, 31–43.

    Google Scholar 

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Pettitt, J.M. A route for the passage of substances through the developing pteridophyte exine. Protoplasma 88, 117–131 (1976). https://doi.org/10.1007/BF01280364

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