Monday, September 2, 2019
Involvement Of K+ In Leaf Movements During Suntracking :: essays research papers
 Involvement of K+ in Leaf Movements During Suntracking      Introduction    à  Ã  Ã  Ã  Ã  Many plants orient their leaves in response to directional light signals.  Heliotropic movements, or movements that are affected by the sun, are common  among plants belonging to the families Malvaceae, Fabaceae, Nyctaginaceae, and  Oxalidaceae. The leaves of many plants, including Crotalaria pallida, exhibit  diaheliotropic movement. C. pallida is a woody shrub native to South Africa.  Its trifoliate leaves are connected to the petiole by 3-4 mm long pulvinules  (Schmalstig). In diaheliotropic movement, the plantââ¬â¢s leaves are oriented  perpendicular to the sunââ¬â¢s rays, thereby maximizing the interception of  photosynthetically active radiation (PAR). In some plants, but not all, his  response occurs particularly during the morning and late afternoon, when the  light is coming at more of an angle and the water stress is not as severe  (Donahue and Vogelmann). Under these conditions the lamina of the leaf is  within less than 15à ° from the normal to the sun. Many plants that exhibit  diaheliotropic movements also show paraheliotropic response as well.  Paraheliotropism minimizes water loss by reducing the amount of light absorbed  by the leaves; the leaves orient themselves parallel to the sunââ¬â¢s rays. Plants  that exhibit paraheliotropic behavior usually do so at midday, when the sunââ¬â¢s  rays are perpendicular to the ground. This reorientation takes place only in  leaves of plants that are capable of nastic light-driven movements, such as the  trifoliate leaf of Erythrina spp. (Herbert 1984). However, this phenomenon has  been observed in other legume species that exhibit diaheliotropic leaf movement  as well. Their movement is temporarily transformed from diaheliotropic to  paraheliotropic. In doing so, the interception of solar radiation is maximized  during the morning and late afternoon, and minimized during midday. The leaves  of Crotalaria pallida also exhibit nyctinastic, or sleep, movements, in which  the leaves fold down at night. The solar tracking may also provide a  competitive advantage during early growth, since there is little shading, and  also by intercepting more radiant heat in the early morning, thus raising leaf  temperature nearer the optimum for photosynthesis.  à  Ã  Ã  Ã  Ã  Integral to understanding the heliotropic movements of a plant is  determining how the leaf detects the angle at which the light is incident upon  it, how this perception is transduced to the pulvinus, and finally, how this  signal can effect a physiological response (Donahue and Vogelmann).  à  Ã  Ã  Ã  Ã  In the species Crotalaria pallida, blue light seems to be the wavelength  that stimulates these leaf movements (Scmalstig). It has been implicated in the  photonastic unfolding of leaves and in the diaheliotropic response in  Mactroptilium atropurpureum and Lupinus succulentus (Schwartz, Gilboa, and  Koller 1987). However, the light receptor involved can not be determined from    					  Involvement Of K+ In Leaf Movements During Suntracking  ::  essays research papers   Involvement of K+ in Leaf Movements During Suntracking      Introduction    à  Ã  Ã  Ã  Ã  Many plants orient their leaves in response to directional light signals.  Heliotropic movements, or movements that are affected by the sun, are common  among plants belonging to the families Malvaceae, Fabaceae, Nyctaginaceae, and  Oxalidaceae. The leaves of many plants, including Crotalaria pallida, exhibit  diaheliotropic movement. C. pallida is a woody shrub native to South Africa.  Its trifoliate leaves are connected to the petiole by 3-4 mm long pulvinules  (Schmalstig). In diaheliotropic movement, the plantââ¬â¢s leaves are oriented  perpendicular to the sunââ¬â¢s rays, thereby maximizing the interception of  photosynthetically active radiation (PAR). In some plants, but not all, his  response occurs particularly during the morning and late afternoon, when the  light is coming at more of an angle and the water stress is not as severe  (Donahue and Vogelmann). Under these conditions the lamina of the leaf is  within less than 15à ° from the normal to the sun. Many plants that exhibit  diaheliotropic movements also show paraheliotropic response as well.  Paraheliotropism minimizes water loss by reducing the amount of light absorbed  by the leaves; the leaves orient themselves parallel to the sunââ¬â¢s rays. Plants  that exhibit paraheliotropic behavior usually do so at midday, when the sunââ¬â¢s  rays are perpendicular to the ground. This reorientation takes place only in  leaves of plants that are capable of nastic light-driven movements, such as the  trifoliate leaf of Erythrina spp. (Herbert 1984). However, this phenomenon has  been observed in other legume species that exhibit diaheliotropic leaf movement  as well. Their movement is temporarily transformed from diaheliotropic to  paraheliotropic. In doing so, the interception of solar radiation is maximized  during the morning and late afternoon, and minimized during midday. The leaves  of Crotalaria pallida also exhibit nyctinastic, or sleep, movements, in which  the leaves fold down at night. The solar tracking may also provide a  competitive advantage during early growth, since there is little shading, and  also by intercepting more radiant heat in the early morning, thus raising leaf  temperature nearer the optimum for photosynthesis.  à  Ã  Ã  Ã  Ã  Integral to understanding the heliotropic movements of a plant is  determining how the leaf detects the angle at which the light is incident upon  it, how this perception is transduced to the pulvinus, and finally, how this  signal can effect a physiological response (Donahue and Vogelmann).  à  Ã  Ã  Ã  Ã  In the species Crotalaria pallida, blue light seems to be the wavelength  that stimulates these leaf movements (Scmalstig). It has been implicated in the  photonastic unfolding of leaves and in the diaheliotropic response in  Mactroptilium atropurpureum and Lupinus succulentus (Schwartz, Gilboa, and  Koller 1987). However, the light receptor involved can not be determined from    					    
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