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Other Real-Time Movement

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Abstract

In the case of root movement, a very interesting phenomenon was found using the Super-HARP camera, which enabled the visualization of root movement in the dark.

Although the first data on plants show that the harmful effect is growth inhibition, the first effect of the toxicity was to stop the rotation movement of the roots before growth inhibition occurred.

When there was a chemical change in the environment, although the circumnutation of the root tip ceased, the root was able to elongate, and it was interesting that after a while the root movement resumed. In the case of a rice root, one round of movement of the rice root tip showed a constant time of approximately 50 minutes. However, this movement ceased when Al ion was supplied. The time needed for resuming the movement of the root tip was dependent on the Al ion concentration. It is not known what triggers the resumption of the movement of the root tip.

Keywords

HARP camera Circumnutation Root movement Moving angle Movement cycle Al 

8.1 Root Movement During Growth (HARP Camera Images in the Dark)

Circumnutation is a rotating movement of a growing plant organ that is considered to result from endogenous rhythmic processes. The regular autonomous rotating movement of a root is due to different growth on the sides of the root, based on oscillators at the cellular or tissue level. However, the mechanisms responsible for circumnutation are still unclear. In particular, because of the lack of imaging tools, it has not been possible to acquire rotating images of roots under dark conditions. Since light has an influence on the physiological activity of the root, such as inducing photosynthesis, the development of devices that enable seeing the root under dark conditions is needed. Since we could use a super-HARP camera developed by the NHK broadcasting technology institute in Japan, we could visualize root circumnutation in the dark.

Four-day-old seedlings of rice plants were grown in water culture, and the super-HARP camera was set outside the phytotron to obtain images of the plant root through the glass window (Fig. 8.1). Images of the root were acquired at an interval of 1 min, and each image was accumulated for 4 s. The culturing room was kept dark, and the root-growing behavior was monitored from the next room. The rice image taken by the camera was analyzed by a computer to calculate the root length as well as root tip angle. Figure 8.2 shows an example image taken by the Super-HARP camera. Although the room was dark, the color image of the sample was shown with high resolution.
Fig. 8.1

Schematic illustration of the root imaging system using a Super-HARP camera in the dark [1]. A rice seedling was placed in the upper part of a glass vessel filled with 0.2 mM CaCl2 solution. The root-growing manner was video-recorded by a Super-HARP camera, and all devices were maintained in the dark at approximately 300 pmol/m2/s (0.02 lux). Since the room was kept in the dark, the root-growing manner was monitored from the next room

Fig. 8.2

An example of the rice root growing image taken by a Super-HARP camera [1]. The color image was taken at 1-min intervals and accumulated for 4 s

It was found that the curvature was initiated in the same region of the root, the elongation zone. The root elongation rate was kept constant with regular rhythmic movement, showing a fixed angle. The successive images of the root while growing in control solution are shown in Fig. 8.3. One round of root tip rotation took approximately 50 minutes.
Fig. 8.3

Images of the circumnutation of a rice root by a Super-HARP camera [1]. (a) Measurement of the angle between the root tip and the direction of root elongation. (b) Successive root images grown in the control solution at pH 4.5, taken by a Super-HARP camera. The curvature was initiated in the same region of the root, which was the upper part of the elongation zone. The root length and rotation angle of the root tip were analyzed from the series of obtained images. The white bar is 1 mm in all images

However, when treated with Al solution, the rotation angle of the root tip was decreased, and then the movement resumed (Fig. 8.4). With increasing Al concentration, the time root rotation was suppressed, i.e., the time until the root resumed the rotating movement was increased. When the AlCl3 concentration was increased to 50 μM, resumption of the rotating movement was not observed even after 7 h. With 5.0 μM Al treatment, inhibition of root tip circumnutation was obtained without inhibiting root elongation (Fig. 8.5). The results offered an interesting suggestion that this new inhibition of root tip circumnutation occurred at lower Al concentrations than the inhibition of root elongation previously reported in studies of Al toxicity. This is a new phase of early reactions of the plant root to Al stress.
Fig. 8.4

Effect of Al on the circumnutation of the root tip [1]. (a), (b), (c), and (d) show the circumnutation profile when the solution was changed to 0, 5, 10, and 50 μM Al, respectively. (1) indicates the control period (2 h); (1*) indicates the control period after renewal of the solution (2 h); (2) indicates the cycle-fading period; (3) indicates the cycle-ceased period. 0 h in each figure indicates when the solution was renewed. The rotation angle was calculated from the apparent maximum oscillation in the successive video images. With 5 μM AlCl3, the maximum rotation angle decreased, and the root rotated again after a while without changing the elongation rate

Fig. 8.5

Root elongation calculated through image analysis [1]. The root elongation was indicated by the relative root length, where 0 mm was set when an Al treatment was performed (at 0 h). With the 5.0-μM Al treatment, the root tip circumnutation was inhibited without inhibiting observable root growth, which suggests that the inhibition of circumnutation is an earlier effect than the inhibition of root elongation. The reason why circumnutation resumes after a time period is unknown

It is known that Al ions induce callose production, as an earliest reaction, damaging plasma membranes and inhibiting root elongation. Our study suggested that the inhibition of root tip circumnutation occurred before callose production, followed by the inhibition of root elongation.

Whole root movement is controlled by the balance of plant hormones, and auxin probably plays a central role in root development because of its cell extension effect. Since auxin extends root cells, it has been supposed that the localization of auxin generates circumnutation. As an alternative, some environmental conditions have been discussed, including the possibility that certain metal ions induce circumnutation.

Circumnutation plays an important role in the effective development of roots in soil structures containing inhomogeneous nutrients. With a rotating root tip, roots are able to select the appropriate direction to extend smoothly. Because of the lack of tools, it was extremely difficult to study root movement in the dark. The Super-HARP camera used in this study allowed the acquisition of images in dark conditions, approximately 300 pmol/m2/s, under which no other optical devices could obtain images. Thus, the observation of root growth using the Super-HARP camera is better than any other method to study root activity in the dark.

Supplementary material

484736_1_En_8_MOESM1_ESM.zip (86 kb)
Supplement.zip (87 kb)

Bibliography

  1. 1.
    Hayashi Y, Nishiyama H, Tanoi K, Ohya T, Nihei N, Tanioka K, Nakanishi TM (2004) An aluminum influence on root circumnutation in dark revealed by a new super-HARP (high-gain avalanche rushing amorphous photoconductor) camera. Plant and Cell Physiology 45:351–356CrossRefGoogle Scholar

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Authors and Affiliations

  1. 1.Graduate School of Agricultural and Life SciencesThe University of TokyoBunkyo-kuJapan

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