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The phenomenon of solar tracking is known from the early studies of Yin (1938) and that it is a blue light response, while the actual photoreceptors involved are not identified (Batschauer 1998; Briggs and Christie, 2002). In view of the fact that solar tracking behaviour results from light-driven turgor changes in the volume of the cells just as in the case of stomatal guard cells, the phototropins might be involved here also (Briggs and Christie, 2002). Sakamoto and Briggs (2002) have suggested that solar tracking may involv e phototropins. The precise molecular mechanisms concernin g the heliotropic movements are not currently known , while some knowledge is available on the mechanism of nyctinastic movements. However, Cronlund and Forseth (1995) have studied the mechanism of soybean leaflet movement and concluded that the mechanism of heliotropic movement was similar to that of nyctinastic movements. These authors have studied the role of K+ channels and the plasma membrane H/ATPase (Michelet and Boutry, 1995) in paraheliotropic movements throug h the measurements of leaf movements after treatment of pulvinus with promoters and inhibitors of HATPase and K+ channels. HATPase inhibition reduced the leaf
DOI link for The phenomenon of solar tracking is known from the early studies of Yin (1938) and that it is a blue light response, while the actual photoreceptors involved are not identified (Batschauer 1998; Briggs and Christie, 2002). In view of the fact that solar tracking behaviour results from light-driven turgor changes in the volume of the cells just as in the case of stomatal guard cells, the phototropins might be involved here also (Briggs and Christie, 2002). Sakamoto and Briggs (2002) have suggested that solar tracking may involv e phototropins. The precise molecular mechanisms concernin g the heliotropic movements are not currently known , while some knowledge is available on the mechanism of nyctinastic movements. However, Cronlund and Forseth (1995) have studied the mechanism of soybean leaflet movement and concluded that the mechanism of heliotropic movement was similar to that of nyctinastic movements. These authors have studied the role of K+ channels and the plasma membrane H/ATPase (Michelet and Boutry, 1995) in paraheliotropic movements throug h the measurements of leaf movements after treatment of pulvinus with promoters and inhibitors of HATPase and K+ channels. HATPase inhibition reduced the leaf
The phenomenon of solar tracking is known from the early studies of Yin (1938) and that it is a blue light response, while the actual photoreceptors involved are not identified (Batschauer 1998; Briggs and Christie, 2002). In view of the fact that solar tracking behaviour results from light-driven turgor changes in the volume of the cells just as in the case of stomatal guard cells, the phototropins might be involved here also (Briggs and Christie, 2002). Sakamoto and Briggs (2002) have suggested that solar tracking may involv e phototropins. The precise molecular mechanisms concernin g the heliotropic movements are not currently known , while some knowledge is available on the mechanism of nyctinastic movements. However, Cronlund and Forseth (1995) have studied the mechanism of soybean leaflet movement and concluded that the mechanism of heliotropic movement was similar to that of nyctinastic movements. These authors have studied the role of K+ channels and the plasma membrane H/ATPase (Michelet and Boutry, 1995) in paraheliotropic movements throug h the measurements of leaf movements after treatment of pulvinus with promoters and inhibitors of HATPase and K+ channels. HATPase inhibition reduced the leaf
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