
doi: 10.1071/fp03089
pmid: 15895503
Gravitropism of vascular plants has been assumed to require a single gravity receptor mechanism. However, based on the evidence in Part I of this study, we propose that maize roots require two. The first mechanism is without a directional effect and, by itself, cannot give rise to tropism. Its role is quantitative facilitation of the second mechanism, which is directional like the gravitational force itself and provides the impetus for tropic curvature. How closely coupled the two mechanisms may be is, as yet, unclear. The evidence for dual receptors supports a general model for roots. When readiness for gravifacilitation, or gravifacilitation itself, is constitutive, orthogravitropic curvature can go to completion. If not constitutively enabled, gravifacilitation can be weak in the absence of light and water deficit or strong in the presence of light and water deficit. In either case, it can decay and permit roots to assume reproducible non-vertical orientations (plagiogravitropic or plagiotropic orientations) without using non-vertical setpoints. In this way roots are deployed in a large volume of soil. Gravitropic behaviours in shoots are more diverse than in roots, utilising oblique and horizontal as well as vertical setpoints. As a guide to future experiments, we assess how constitutive v. non-constitutive modes of gravifacilitation might contribute to behaviours based on each kind of setpoint.
Avena, Indoleacetic Acids, Light, Arabidopsis, Temperature, Biological Transport, Inositol 1,4,5-Trisphosphate, Hydrogen-Ion Concentration, Plant Roots, Zea mays, Gravitropism, Gravity Sensing, Plant Shoots, Abscisic Acid
Avena, Indoleacetic Acids, Light, Arabidopsis, Temperature, Biological Transport, Inositol 1,4,5-Trisphosphate, Hydrogen-Ion Concentration, Plant Roots, Zea mays, Gravitropism, Gravity Sensing, Plant Shoots, Abscisic Acid
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