Skip to main content
Log in

The development of the placenta in the anthocerote Phaeoceros laevis (L.) Prosk

  • Published:
Planta Aims and scope Submit manuscript

Abstract

The development of the placenta in the anthocerote Phaeoceros laevis (L.) Prosk. was studied by transmission electron microscopy. By the time the sporophyte emerges from the involucre, a conspicuous placental region is formed by the intrusive growth of sporophyte foot haustorial cells into the adjacent gametophyte vaginula tissue. The separation of gametophyte cells by haustorial cells and their incorporation into the placenta are preceded by the loosening and swelling of their walls and the formation of a periplasmic space. This process causes the disruption of the plasmodesmata, and may eventually result in the complete isolation and consequent degeneration of the cells. Crystals are commonly observed in the vacuoles of gametophyte placental cells. Crystals become more abundant during cytoplasmic degeneration, and are released in the placental lacunae that result from the complete dissolution of gametophyte cells. During the subsequent phase of capsule elongation, the gametophyte placental cells that retain the symplastic connection with the adjoining gametophyte parenchyma develop a wall labyrinth typical of transfer cells. Obliteration of the wall labyrinth by deposition of lightly staining wall material is observed later in sporophyte development, in concomitance with capsule dehiscence. Crystals are negative to the periodic acid/thiocarbohydrazide/silver proteinate test for carbohydrates whilst they are completely digested by pepsin or protease, denoting protein composition.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

PATAg:

periodic acid/thiocarbohydrazide/silver proteinate

References

  • Ben-Arie, R., Kislev, N., Frenkel, C. (1979) Ultrastructural changes in the cell walls of ripening apple and pear fruit. Plant Physiol. 64, 197–202

    Google Scholar 

  • Bhavannarayana, K., Metha, P.M., Kothari, I.L. (1982) Ultrastructural studies in the pericarp of unripened and ripened tomato fruits. Bull. Soc. Bot. Fr. 129, 13–19

    Google Scholar 

  • Browning, A.J., Gunning, B.E.S. (1979) Structure and function of transfer cells in the sporophyte haustorium of Funaria hygrometrica. I. The development and ultrastructure of the haustorium. J. Exp. Bot. 30, 1233–1246

    Google Scholar 

  • Esau, K., Torsch, J. (1984) The sieve plate of Echium (Boraginaceae): Developmental aspects and response of P—protein to protein digestion. J. Ultrastruct. Res. 86, 31–45

    Google Scholar 

  • Eymé, J., Suire, C. (1967) Au suject de l'infrastructure de la zone placentaire de Mnium cuspidatum Hedw. (mousse bryale acrocarpe). C.R. Acad. Sci. Paris, Sér. D 265, 1788–1791

    Google Scholar 

  • Fineran, B.A., Bullock, S. (1979) Ultrastructure of graniferous tracheary elements in the haustorium of Exocarpus bidwillii, a root hemi-parasite of the Santalaceae. Proc. R. Soc. London B 204, 329–343

    Google Scholar 

  • Gambardella, R. (1987) Ultrastructure and development of the gametophyte vaginula-sporophyte foot complex in the liverwort Targionia hypophylla. Planta 172, 431–438

    Google Scholar 

  • Gambardella, R., de Lucia Sposito, M.L. (1981–1982) Ultrastructure of the placental region in a liverwort, Mannia androgyna. Delpinoa 23–24, 177–184

    Google Scholar 

  • Gambardella, R., de Lucia Sposito, M.L. (1983) Placenta ultrastructure in Plagiochasma rupestre (Forst.) Steph. (Marchantiales, Hepaticae). G. Bot. Ital. 177, 166–167

    Google Scholar 

  • Gambardella, R., Ligrone, R., Castaldo, R. (1981) Ultrastructure of the sporophyte foot in Phaeoceros. Cryptog. Bryol. Lichenol. 2, 23–45

    Google Scholar 

  • Hébant, C. (1975) Organization of the conducting tissue-system in the sporophytes of Dawsonia and Dendroligotrichum (Polytrichales, Musci). J. Hattori Bot. Lab. 39, 235–254

    Google Scholar 

  • Kelley, C. (1969) Wall projections in the sporophyte and gametophyte of Sphaerocarpos. J. Cell Biol. 41, 910–914

    Google Scholar 

  • Lal, M., Chauhan, E. (1981) Transfer cells in the sporophytegametophyte junction of Physcomitrium cyathycarpum. Protoplasma 107, 79–83

    Google Scholar 

  • Ligrone, R., Gambardella, R., Castaldo, R., Giordano, S., de Lucia Sposito, M.L. (1982a) Gametophyte and sporophyte ultrastructure in Buxbaumia piperi Best (Buxbaumiales, Musci). J. Hattori Bot. Lab. 52, 465–499

    Google Scholar 

  • Ligrone, R., Gambardella, R., de Lucia Sposito, M.L. (1982b) Ultrastructure of the sporophyte foot-gametophyte vaginula complex in Timmiella barbuloides (Brid.) Moenk. Planta 154, 414–425

    Google Scholar 

  • Maier, K. (1967) Wandlabyrinthe in Sporophyten von Polytrichum. Planta 77, 108–126

    Google Scholar 

  • Maier, K., Maier, U. (1972) Localization of beta-glycerophosphatase and Mg++-activated adenosine triphosphatase in a moss haustorium, and the relation of these enzymes to the cell wall labyrinth. Protoplasma 75, 91–112

    Google Scholar 

  • Marsh, B.H., Doyle, W.T. (1985) Intercellular protein crystals from the gametophyte-sporophyte junction of the hornwort Phaeoceros laevis Prosk. Protoplasma 129, 223–226

    Google Scholar 

  • Matile, P. (1974) Lysosomes. In: Dynamic aspects of plant ultrastructure, pp. 178–218, Robards, A.W., ed. McGraw Hill, London

    Google Scholar 

  • O'Brien, T.P. (1970) Further observations on hydrolysis of the cell wall in the xylem. Protoplasma 69, 1–14

    Google Scholar 

  • Roland, J.C., Sandoz, D. (1969) Détection cytochimique des sites de formation des polysaccharides prémembranaires dans les cellules végétales. J. Microsc. 2, 263–268

    Google Scholar 

  • Sexton, R., Jameson, G.G.C., Allan, M.H.J.L. (1977) An ultrastructural study of abscission zone cells with special reference to the mechanism of enzyme secretion. Protoplasma 91, 369–387

    Google Scholar 

  • Spurr, A.R. (1969) A low-viscosity epoxy resin embedding medium for electron microscopy. J. Ultrastruct. Res. 26, 31–34

    Google Scholar 

  • Thomas, R.J., Stanton, D.S., Longendorfer, D.H., Farr, M.E. (1978) Physiological evaluation of the nutritional autonomy of a hornwort sporophyte. Bot. Gaz. 139, 306–311

    Google Scholar 

  • Wiencke, C., Schulz, D. (1978) The development of transfer cells in the haustorium of the Funaria hygrometrica sporophyte. Bryophyt. Biblioth. 13, 147–167

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Gambardella, R., Ligrone, R. The development of the placenta in the anthocerote Phaeoceros laevis (L.) Prosk. Planta 172, 439–447 (1987). https://doi.org/10.1007/BF00393859

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00393859

Key words

Navigation