Skip to main content Accessibility help
×
Hostname: page-component-76fb5796d-vvkck Total loading time: 0 Render date: 2024-04-28T07:19:34.403Z Has data issue: false hasContentIssue false

Chapter 8 - The epidermis

Published online by Cambridge University Press:  05 June 2012

Charles B. Beck
Affiliation:
University of Michigan, Ann Arbor
Get access

Summary

Perspective

Most terrestrial plants live in a highly evaporative environment and one in which they are constantly exposed to toxic substances, to attack and invasion by various small insects and pathogens, to the potentially damaging effects of solar radiation, and to potential damage from high winds. Consequently, several protective tissues have evolved that reduce water loss from the plant, restrict the entry of organisms and toxic substances into the plant body, mitigate the effects of radiation, and strengthen and support the plant thereby reducing its susceptibility to damage from rapid air movement. These include the epidermis of shoot and root systems (sometimes called rhizodermis in the root), the periderm and the rhytidome. These tissues, while providing these functions, must also under certain conditions allow oxygen used in respiration to enter the plant and carbon dioxide utilized in photosynthesis to exit the plant. Consequently, the epidermis and other surficial, protective tissues represent both structural and functional compromises. As the bounding tissue of all young parts of a plant, and of the aerial parts of plants that are comprised solely or largely of primary tissues, the epidermis also provides an important supporting function. In the stem of Tulipa (tulip), for example, the epidermis plus a layer of subepidermal collenchyma can contribute as much as 50% to overall stem stiffness (Niklas and Paolillo, 1997). We shall consider the epidermis in some detail in this chapter, and periderm and rhytidome in Chapter 13.

Type
Chapter
Information
An Introduction to Plant Structure and Development
Plant Anatomy for the Twenty-First Century
, pp. 138 - 153
Publisher: Cambridge University Press
Print publication year: 2005

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Amarsinghe, V.Graham, S. A., and Graham, A.. 1991. Trichome morphology in the genus Cuphea (Lythraceae). Bot. Gaz. 152: 77–90CrossRefGoogle Scholar
Apostolakos, P. and Galatis, B.. 1999. Microtubule and actin filament organization during stomatal morphogenesis in the fern Asplenium nidus. II. Guard cells. New Phytol. 141: 209–223CrossRefGoogle Scholar
Barnes, J. D. and J. Cadoso-Vilhena. 1996. Interactions between electromagnetic radiation and the plant cuticle. In Kerstiens, G. ed., Plant Cuticles: An Integrated Functional Approach. Oxford, UK: Bios Scientific Publishers, pp. 157–174Google Scholar
Bowman, J. 1994. Arabidopsis: An Atlas of Morphology and Development. Heidelberg: Springer-VerlagGoogle Scholar
Carr, D. J. and Carr, S. G. M.. 1991. Development of the stomatal complexes during ontogeny in Eucalyptus and Angophora (Myrtaceae). Austral. J. Bot. 39: 43–58CrossRefGoogle Scholar
Dávilla, P. and Clark, L. G.. 1990. Scanning electron microscopy survey of leaf epidermis of Sorghastrum (Poaceae: Andropogoneae). Am. J. Bot. 77: 499–511CrossRefGoogle Scholar
Jenks, M. A., Rich, P. J., Peters, P. J., Axtell, J. D., and Ashworth, E. N.. 1992. Epicuticular wax morphology of bloomless (bm) mutants in Sorghum bicolor. Int. J. Plant Sci. 153: 311–319CrossRefGoogle Scholar
Juniper, B. E. 1959. The surfaces of plants. Endeavour 18: 20–25CrossRefGoogle Scholar
Kaufman, P. B., Petering, L. B., Yocum, C. S., and Baic, D.. 1970. Ultrastructural studies on stomata development in internodes of Avena sativa. Am. J. Bot. 57: 33–49CrossRefGoogle Scholar
Metcalfe, C. R. and Chalk, L.. 1950. Anatomy of the Dicotyledons, 2 vols. Oxford, UK: Clarendon PressGoogle Scholar
Neinhuis, C. and Barthlott, W.. 1997. Characterization and distribution of water-repellent, self-cleaning plant surfaces. Ann. Bot. 79: 667–677CrossRefGoogle Scholar
Neinhuis, C., Koch, K., and Barthlott, W.. 2001. Movement and regeneration of epicuticular waxes through plant cuticles. Planta 213: 427–434CrossRefGoogle ScholarPubMed
Niklas, K. J. and Paolillo, D. J. Jr. 1997. The role of the epidermis as a stiffening agent in Tulipa (Liliaceae) stems. Am. J. Bot. 84: 735–744CrossRefGoogle ScholarPubMed
Panteris, E., Apostolakos, P., and Galatis, B.. 1994. Sinuous ordinary epidermal cells: behind several patterns of waviness, a common morphogenetic mechanism. New Phytol. 127: 771–780CrossRefGoogle Scholar
Stockey, R. and Ko, H.. 1990. Cuticle micromorphology of Dacrydium (Podocarpaceae) from New Caledonia. Bot. Gaz. 151: 138–149CrossRefGoogle Scholar
Stockey, R.,Frevel, B. J., and Woltz, P.. 1998. Cuticle micromorphology of Podocarpus, subgenus Podocarpus, section Scytopodium (Podocarpaceae) of Madagascar and South Africa. Int. J. Plant Sci. 159: 923–940CrossRefGoogle Scholar
Tenberge, K. B. 1991. Ultrastructure and development of the outer epidermal wall of spruce (Picea abies) needles. Can. J. Bot. 70: 1467–1487CrossRefGoogle Scholar
Troughton, D. and , L. A. Donaldson. 1972. Probing Plant Structure. New York: McGraw-HillGoogle Scholar
Wojtaszek, P. 2000. Genes and plant cell walls: a difficult relationship. Biol. Rev. 75: 437–475CrossRefGoogle ScholarPubMed
Behnke, H.-D. 1984. Plant trichomes – structure and ultrastructure: general terminology, taxonomic applications, and aspects of trichome-bacteria interaction in leaf tips of Dioscorea. In Rodriguez, E, Healey, P. L., and Mehta, I., eds., Biology and Chemistry of Plant Trichomes. New York: Plenum Press, pp. 1–21CrossRefGoogle Scholar
Cutler, D. F., Alvin, K. L., and Price, C. E. (eds.) 1982. The Plant Cuticle. London: Academic PressGoogle Scholar
Davis, D. G. 1971. Scanning electron microscopic studies of wax formation on leaves of higher plants. Can. J. Bot. 49: 643–546CrossRefGoogle Scholar
Eglington, G. and Hamilton, R. J.. 1967. Leaf epicuticular waxes. Science 156: 1322–1335CrossRefGoogle Scholar
Esau, K. 1965. Plant Anatomy, 2nd edn. New York: John Wiley and SonsGoogle Scholar
Juniper, B. E. and Jeffree, C. E.. 1983. Plant Surfaces. London: Edward ArnoldGoogle Scholar
Kerstiens, G. (ed.) 1996. Plant Cuticles: An Integrated Functional Approach. Oxford, UK: BIOS Scientific PublishersGoogle Scholar
Koch, K., Neinhuis, C., Ensikat, H. J., and Barthlott, W.. 2004. Self assembly of epicuticular waxes on living plant surfaces imaged by atomic force microscopy (AFM). J. Exp. Bot. 55: 711–718CrossRefGoogle Scholar
Levitt, J. 1974. The mechanism of stomatal movement: once more. Protoplasma 82: 1–17CrossRefGoogle Scholar
Mansfield, T. A., Hetherington, A. M., and Atkinson, C. J.. 1990. Some current aspects of stomatal physiology. Annu. Rev. Plant Physiol. Plant Mol. Biol. 41: 55–75CrossRefGoogle Scholar
Martin, J. T. and Juniper, B. E.. 1970. The Cuticles of Plants. London: Edward ArnoldGoogle Scholar
Pant, D. D. 1965. On the ontogeny of stomata and other homologous structures. Plant Sci. Ser. Allahabad 1: 1–24Google Scholar
Raschke, K. 1975. Stomatal action. Annu. Rev. Plant Physiol. 26: 309–340CrossRefGoogle Scholar
Romberger, J. A., Hejnowicz, Z., and Hill, J. F.. 1993. Plant Structure: Function and Development. Berlin: Springer-VerlagCrossRefGoogle Scholar
Sachs, T. and Novoplansky, N.. 1993. The development and patterning of stomata and glands in the epidermis of Peperomia. New Phytol. 123: 567–574CrossRefGoogle Scholar
Srivastava, L. M. and Singh, A. P.. 1972. Stomatal structure in corn leaves. J. Ultrastruct. Res. 39: 345–363CrossRefGoogle ScholarPubMed
Uphof, J. C. T. 1962. Handbuch der Pflanzenanatomie, vol. 4, part 5, Plant hairs. Berlin: Gebrüder BorntraegerGoogle Scholar

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

  • The epidermis
  • Charles B. Beck, University of Michigan, Ann Arbor
  • Book: An Introduction to Plant Structure and Development
  • Online publication: 05 June 2012
  • Chapter DOI: https://doi.org/10.1017/CBO9781139165365.009
Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

  • The epidermis
  • Charles B. Beck, University of Michigan, Ann Arbor
  • Book: An Introduction to Plant Structure and Development
  • Online publication: 05 June 2012
  • Chapter DOI: https://doi.org/10.1017/CBO9781139165365.009
Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

  • The epidermis
  • Charles B. Beck, University of Michigan, Ann Arbor
  • Book: An Introduction to Plant Structure and Development
  • Online publication: 05 June 2012
  • Chapter DOI: https://doi.org/10.1017/CBO9781139165365.009
Available formats
×