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Chapter 12 - Growth movements

Published online by Cambridge University Press:  05 June 2012

Helgi Öpik
Affiliation:
University of Wales, Swansea
Stephen A. Rolfe
Affiliation:
University of Sheffield
Arthur J. Willis
Affiliation:
University of Sheffield
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Summary

Introduction

Although it is a general perception that plants do not move very much, or very quickly, this is true only when seen from a human perspective. If we view the world using time-lapse photography we quickly become aware that all plants are, more or less, in continuous motion. This should not come as a surprise when one considers that plants cannot uproot themselves and relocate to a new environment to maintain suitable conditions; they must orientate their organs, largely by growth, to optimize their interactions with the non-uniform environment which surrounds them. We tend to take it for granted that shoots (usually) grow upwards into the air and roots grow down into the ground; leaves spread out and turn to the light; flowers take up specific orientations. All this positioning is the result of differential growth, growth movements, in precise and complex responses to environmental stimuli, especially light and gravity. Mutants which lack some of these responses are unable to grow normally; e.g. mutant shoots unable to respond to gravity lie on the ground and in the field would be overgrown and perish. Growth movements, imperceptible as they are to instantaneous observation, are vital to the plant. In addition to the relatively slow growth movements, more rapid, visible movements are exhibited by specialized plant organs.

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Publisher: Cambridge University Press
Print publication year: 2005

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References

Journal of Plant Growth Regulation, 21(2) (2002). Issue largely devoted to tropisms, particularly gravitropism.
Boonsirichai, K., Guan, C., Chen, R. & Masson, P. H.Root gravitropism: an experimental tool to investigate basic cellular and molecular processes underlying mechanosensing and signal transmission in plants. Annual Review of Plant Biology, 53 (2002), 421–47.CrossRefGoogle ScholarPubMed
Kagawa, T. & Wada, M.Blue light-induced chloroplast relocation. Plant Cell Physiology, 43 (2002), 367–71.CrossRefGoogle ScholarPubMed
Sack, F. D.Plastids and gravitropic sensing. Planta, 203 (1997), S63–8.CrossRefGoogle ScholarPubMed
Ahmad, M., Jarillo, J. A., Smirnova, O. & Cashmore, A. R. (1998). Cryptochrome blue-light photoreceptors of Arabidopsis implicated in phototropism. Nature, 392, 720–3.CrossRefGoogle ScholarPubMed
Bell, C. J. & Maher, E. P. (1990). Mutants of Arabidopsis thaliana with abnormal gravitropic responses. Molecular & General Genetics, 220, 289–93.CrossRefGoogle Scholar
Briggs, W. R. & Christie, J. M. (2002). Phototropins 1 and 2: versatile plant blue-light receptors. Trends in Plant Science, 7, 204–10.CrossRefGoogle ScholarPubMed
Collings, D. A., Zsuppan, G., Allen, N. S. & Blancaflor, E. B. (2001). Demonstration of prominent actin filaments in the root columella. Planta, 212, 392–403.CrossRefGoogle ScholarPubMed
Crosson, S. & Moffat, K. (2001). Structure of a flavin-binding plant photoreceptordomain: insights into light-mediated signal transduction. Proceedings of the National Academy of Sciences (USA), 98, 2995–3000.CrossRefGoogle ScholarPubMed
Digby, J. & Firn, R. D. (2002). Light modulation of the gravitropic set-point angle (GSA). Journal of Experimental Botany, 53, 377–81.CrossRefGoogle Scholar
Firn, R. D., Wagstaff, C. & Digby, J. (2000). The use of mutants to probe models of gravitropism. Journal of Experimental Botany, 51, 1323–40.CrossRefGoogle ScholarPubMed
Friml, J., Wisniewska, J., Benkova, E., Mendgen, K. & Palme, K. (2002). Lateral relocation of auxin efflux regulator PIN3 mediates tropism in Arabidopsis. Nature, 415, 806–9.CrossRefGoogle ScholarPubMed
Hasegawa, K., Sakoda, M. & Bruinsma, J. (1989). Revision of the theory of phototropism in plants: a new interpretation of a classical experiment. Planta, 178, 540–4.CrossRefGoogle ScholarPubMed
Jarillo, J. A., Gabrys, H., Capel, J., Alonso, J. M., Ecker, J. R. & Cashmore, A. R. (2001). Phototropin-related NPL1 controls chloroplast relocation induced by blue light. Nature, 410, 952–4.CrossRefGoogle ScholarPubMed
Kagawa, T., Sakai, T., Suetsugu, N.et al. (2001). Arabidopsis NPL1: a phototropin homolog controlling the chloroplast high-light avoidance response. Science, 291, 2138–41.CrossRefGoogle ScholarPubMed
Kaldewey, H. (1957). Wuchsstoffbildung und Nutationsbewegungen von Fritillaria meleagris L. im Laufe der Vegetationsperiode. Planta, 49, 300–44.CrossRefGoogle Scholar
Kinoshita, T., Doi, M., Suetsugu, N., Kagawa, T., Wada, M. & Shimazaki, K. (2001). phot1 and phot2 mediate blue light regulation of stomatal opening. Nature, 414, 656–60.CrossRefGoogle ScholarPubMed
Kiss, J. Z., Wright, J. B. & Caspar, T. (1996). Gravitropism in roots of intermediate-starch mutants of Arabidopsis. Physiologia Plantarum, 97, 237–44.CrossRefGoogle ScholarPubMed
Kuznetsov, O. A. & Hasenstein, K. H. (1996). Intracellular magnetophoresis of amyloplasts and induction of root curvature. Planta, 198, 87–94.CrossRefGoogle ScholarPubMed
Kuznetsov, O. A. & Hasenstein, K. H. (1997). Magnetophoretic induction of curvature in coleoptiles and hypocotyls. Journal of Experimental Botany, 48, 1951–7.CrossRefGoogle ScholarPubMed
Larsen, P. (1962). In Encyclopedia of Plant Physiology, ed. Ruhland, W.. Berlin: Springer. Vol. 17, part 2, pp. 34–73.Google Scholar
Lascève, G., Leymarie, J., Olney, M. A.et al. (1999). Arabidopsis contains at least four independent blue-light-activated signal transduction pathways. Plant Physiology, 120, 605–14.CrossRefGoogle ScholarPubMed
Leitz, G., Schnepf, E. & Greulich, K. O. (1995). Micromanipulation of statoliths in gravity-sensing Chara rhizoids by optical tweezers. Planta, 197, 278–88.CrossRefGoogle ScholarPubMed
Li, Y., Hagen, G. & Guilfoyle, T. J. (1991). An auxin-responsive promoter is differentially induced by auxin gradients during tropisms. The Plant Cell, 3, 1167–75.CrossRefGoogle ScholarPubMed
Liscum, E. & Briggs, W. R. (1995). Mutations in the Nph1 locus of Arabidopsis disrupt the perception of phototropic stimuli. The Plant Cell, 7, 473–85.CrossRefGoogle ScholarPubMed
McClure, B. A. & Guilfoyle, T. (1987). Characterization of a class of small auxin-inducible soybean polyadenylated RNAs. Plant Molecular Biology, 9, 611–23.CrossRefGoogle ScholarPubMed
Okada, K., Ueda, J., Komaki, M. K., Bell, C. J. & Shimura, Y. (1991). Requirement of the auxin polar transport system in early stages of Arabidopsis floral bud formation. The Plant Cell, 3, 677–84.CrossRefGoogle ScholarPubMed
Ottenschläger, I., Wolff, P., Wolverton, C.et al. (2003). Gravity-regulated differential auxin transport from columella to lateral root cap cells. Proceedings of the National Academy of Sciences (USA), 100, 2987–91.CrossRefGoogle ScholarPubMed
Plieth, C. & Trewavas, A. J. (2002). Reorientation of seedlings in the earth's gravitational field induces cytosolic calcium transients. Plant Physiology, 129, 786–96.CrossRefGoogle ScholarPubMed
Sack, F. D. (1997). Plastids and gravitropic sensing. Planta, 203, S63–8.CrossRefGoogle ScholarPubMed
Sakai, T., Kagawa, T., Kasahara, M.et al. (2001). Arabidopsis nph1 and npl1: blue light receptors that mediate both phototropism and chloroplast relocation. Proceedings of the National Academy of Sciences (USA), 98, 6969–74.CrossRefGoogle ScholarPubMed
Sievers, A. & Volkmann, D. (1972). Verursacht differentieller Druck der Amyloplasten auf ein komplexes Endomembransystem die Geoperzeption in Wurzeln?Planta, 102, 160–72.CrossRefGoogle Scholar
Steyer, B. (1967). Die Dosis-Wirkungsrelationen bei geotropen und phototropen Reizung: Vergleich Von Mono- mit Dicotyledonen. Planta, 77, 277–86.CrossRefGoogle Scholar
Stowe-Evans, E. L., Luesse, D. R. & Liscum, E. (2001). The enhancement of phototropin-induced phototropic curvature in Arabidopsis occurs via a photoreversible phytochrome A-dependent modulation of auxin responsiveness. Plant Physiology, 126, 826–34.CrossRefGoogle Scholar
Thimann, K. V. & Curry, G. M. (1961). Phototropism. In Light and Life, ed. McElroy, W. D. & Glass, B.. Baltimore, MD: Johns Hopkins University Press, pp. 646–72.Google Scholar
Doorn, W. G. & Meeteren, U. (2003). Flower opening and closure: a review. Journal of Experimental Botany, 54, 1801–12.CrossRefGoogle ScholarPubMed
Went, F. W. & Thimann, K. V. (1937). Phytohormones. New York, NY: Macmillan.Google Scholar
Whippo, C. W. & Hangarter, R. P. (2003). Second positive phototropism results from coordinated co-action of the phototropins and cryptochromes. Plant Physiology, 132, 1499–1507.CrossRefGoogle ScholarPubMed
Yamamoto, K. T. (2003). Happy end in sight after 70 years of controversy. Trends in Plant Science, 8, 359–60.CrossRefGoogle ScholarPubMed

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  • Growth movements
  • Helgi Öpik, University of Wales, Swansea, Stephen A. Rolfe, University of Sheffield
  • Edited in consultation with Arthur J. Willis, University of Sheffield
  • Book: The Physiology of Flowering Plants
  • Online publication: 05 June 2012
  • Chapter DOI: https://doi.org/10.1017/CBO9781139164450.013
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  • Growth movements
  • Helgi Öpik, University of Wales, Swansea, Stephen A. Rolfe, University of Sheffield
  • Edited in consultation with Arthur J. Willis, University of Sheffield
  • Book: The Physiology of Flowering Plants
  • Online publication: 05 June 2012
  • Chapter DOI: https://doi.org/10.1017/CBO9781139164450.013
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.

  • Growth movements
  • Helgi Öpik, University of Wales, Swansea, Stephen A. Rolfe, University of Sheffield
  • Edited in consultation with Arthur J. Willis, University of Sheffield
  • Book: The Physiology of Flowering Plants
  • Online publication: 05 June 2012
  • Chapter DOI: https://doi.org/10.1017/CBO9781139164450.013
Available formats
×