Stomatal movements and long-distance signaling in plants

References

• Shinozaki K, Yamaguchi-Shinozaki K. Gene expression and signal transduction in water-stress response. Plant Physiol 1997; 115:327 - 334
   PubMed Web of Science ®Google Scholar
• Hasegawa PM, Bressan RA, Zhu JK, Bohnert HJ. Plant cellular and molecular responses to high salinity. Ann Rev Plant Physiol Plant Mol Biol 2000; 51:463 - 499
   PubMed Web of Science ®Google Scholar
• Zhu JK. Salt and drought stress signal transduction in plants. Ann Rev Plant Biol 2002; 53:247 - 273
   PubMed Web of Science ®Google Scholar
• Davies WJ, Zhang J. Root signals and the regulation of growth and development of plants in drying soil. Annu Rev Plant Physinl Plant Mo1 Biol 1991; 42:55 - 76
   Web of Science ®Google Scholar
• Wilkinson S. pH as a stress signal. Plant Growth Regul 1999; 29:87 - 99
   Web of Science ®Google Scholar
• Ren H, Wei KF, Jia WS, Davies WJ, Zhang J. Modulation of root signals in relation to stomatal sensitivity to root-sourced ABA in droughted plants. J Integ Plant Biol 2007; 49:1413 - 1421
   Web of Science ®Google Scholar
• Lou CH. Kung SD, Yang SF. Integrated action in plant irritability. Discoveries in Plant Biology 1998; 2:Singapore World Scientific 327 - 347
   Google Scholar
• Blackman PG, Davies WJ. Root to shoot communication in maize plants of the effects of soil drying. J Exp Bot 1985; 36:39 - 48
   Web of Science ®Google Scholar
• Passioura JB. Water transport in and to roots. Ann Rev Plant Physiol Plant Mol Biol 1988; 39:245 - 265
   Web of Science ®Google Scholar
• Jones RJ, Mansfield TA. Suppression of stomatal opening in leaves treated with abscisic acid. J Exp Bot 1970; 21:714 - 719
   Web of Science ®Google Scholar
• Wright STC. The relationship between leaf water potential and levels of abscisic acid and ethylene in excised wheat leaves. Planta 1977; 134:183 - 189
   PubMed Web of Science ®Google Scholar
• Zhang J, Davies WJ. Abscisic acid produced in dehydrating roots may enable the plant to measure the water status of the soil. Plant Cell Environ 1989; 12:73 - 81
   Web of Science ®Google Scholar
• Zhang J, Davies WJ. Changes in the concentration of ABA in xylem sap as a function of changing soil water status com account for changes in leaf conductance and growth. Plant Cell Environ 1990; 13:271 - 285
   Web of Science ®Google Scholar
• Zhang J, Davies WJ. Antitranspirant activity in the xylem sap of maize plants. J Exp Bot 1991; 42:317 - 321
   Web of Science ®Google Scholar
• Davies WJ, Tardieu F, Trejo CL. How do chemical signals work in plants that grow in drying soil?. Plant Physiol 1994; 104:309 - 314
   PubMed Web of Science ®Google Scholar
• Khalil AAM, Grace J. Does xylem ABA control the stomatal behaviour of water-stressed sycamore (Acer pseudoplatanus L.) seedlings?. J Exp Bot 1993; 44:1127 - 1134
   Web of Science ®Google Scholar
• Holbrook NM, Shashidhar VR, James RA, Munns R. Stomatal control in tomato with ABA-deficient response of grafted plants to soil drying. J Exp Bot 2002; 53:1503 - 1514
   PubMed Web of Science ®Google Scholar
• Munns R, King RW. ABA is not the only stomatal inhibitor in transpiration stream of wheat plants. Plant Physiol 1988; 88:703 - 708
   PubMed Web of Science ®Google Scholar
• Wikinson S, Davies WJ. ABA-based chemical signaling: the co-ordination of responses to stress in plants. Plant Cell Environ 2002; 25:195 - 210
   PubMed Web of Science ®Google Scholar
• Jiang F, Hartung W. Long-distance signalling of abscisic acid (ABA): the factors regulating the intensity of the ABA signal. J Exp Bot 2008; 59:37 - 43
   PubMed Web of Science ®Google Scholar
• Montero E, Cabot C, Poschenrieder C, Barcelo J. Relative importance of osmotic-stress and ion-specific effects on ABA-mediated inhibition of leaf expansion growth in Phaseolus vulgaris. Plant Cell Environ 1998; 21:54 - 62
   Web of Science ®Google Scholar
• Sauter A, Dietz KJ, Hartung W. A possible stress physiological role of abscisic acid conjugates in root-to-shoot signaling. Plant Cell Environ 2002; 25:223 - 228
   PubMed Web of Science ®Google Scholar
• Jackson MB, Hall KC. Early stomatal cosure in water-logged pea plants is mediated by abscisic acid in the absent of foliar water deficits. Plant Cell Environ 1987; 10:121 - 130
   Web of Science ®Google Scholar
• Jackson MB. Long-distance signaling from roots to shoots assessed: the flooding story. J Exp Bot 2002; 53:175 - 181
   PubMed Web of Science ®Google Scholar
• Else MA, Tiekstra AE, Croker SJ, Davies WJ, Jackson MB. Stomatal closure in flooded tomato plants involves abscisic acid and a chemically unidentified anti-transpirant in xylem sap. Plant Physiol 1996; 112:239 - 247
   PubMed Web of Science ®Google Scholar
• Zhang SQ, Outlaw WHJR. Abscisic acid introduced into the transpiration stream accumulates in the guard-cell apoplast and causes stomatal closure. Plant Cell Environ 2001; 24:1045 - 1054
   Web of Science ®Google Scholar
• Wilkinson S, Davies WJ. Xylem sap pH increase: a drought signal received at the apoplastic face of the guard cell that involves the suppression of saturable abscisic acid uptake by the epidermal symplast. Plant Physiol 1997; 113:559 - 573
   PubMed Web of Science ®Google Scholar
• Jia WS, Davies WJ. Modification of leaf apoplastic pH in relation to stomatal sensitivity to root-sourced abscisic acid signals. Plant Physiol 2007; 143:68 - 77
   PubMed Web of Science ®Google Scholar
• Sperry JS, Hacke UG, Oren R, Comstock JP. Water deficits and hydraulic limits to leaf water supply. Plant Cell Environ 2002; 25:251 - 263
   PubMed Web of Science ®Google Scholar
• Yao C, Moreshet S, Aloni B. Water relations and hydraulic control of stomatal behavior in bell pepper plant in partial soil drying. Plant Cell Envrion 2001; 24:227 - 235
   Web of Science ®Google Scholar
• Fuchs EE, Livingston NJ. Hydraulic control of stomatal conductance in Doughlas fir and alder seedlings. Plant Cell Environ 1996; 19:1091 - 1098
   Web of Science ®Google Scholar
• Comstock JP. Hydraulic and chemical signaling in the control of stomatal conductance and transpiration. J Exp Bot 2002; 53:195 - 200
   PubMed Web of Science ®Google Scholar
• Saliendra NZ, Sperry JS, Comstock JP. Influence of leaf water status on stomatal response to humidity, hydraulic conductance and soil drought in Betula occidentalis. Planta 1995; 196:357 - 366
   Web of Science ®Google Scholar
• Tardieu F, Zhang J, Davies WJ. What infonnation is conveye by an ABA signal from maize roots in drying field soil?. Plant Cell Environ 1992; 15:185 - 191
   Web of Science ®Google Scholar
• Tardieu F, Davies WJ. Integration of hydraulic and chemical signaling in the control of stomatal. Plant Cell Environ 1993; 16:341 - 349
   Web of Science ®Google Scholar
• Yang SJ, Huang CL, Wu ZY, Hu JF, Li TZ, Liu SG, Jia W. Stomatal movement in response to long distance-communicated signals initiated by heat shock in partial roots of Commelina communis L. Science in China 2006; 49:1 - 8
   Google Scholar
• Lang ARG, Klepper B, Cumming MJ. Leaf water balance during oscillation of stomatal aperature. Plant Physiol 1969; 44:826 - 830
   PubMed Web of Science ®Google Scholar
• Barrs HD. Cyclic variations in stomatal aperture, transpiration and leaf water potential under constant environmental conditions. Ann Rev Plant Physiol 1971; 22:223 - 236
   Google Scholar
• Ehrler WL, Nakayama FS, Bavel CHMV. Cyclic changes in water balance and transpiration of cotton leaves in a steady environment. Physiol Plant 1965; 18:766 - 775
   Web of Science ®Google Scholar
• Steppe K, Dzikiti S, Lemeur R, Milford JR. Stomatal oscillations in orange trees under natural climatic conditions. Ann Bot 2006; 97:831 - 835
   PubMed Web of Science ®Google Scholar
• Schroeder JI, Allen GJ, Hugouvieux V, Kwak JM, Waner D. Guard cell signal transduction. Ann Rev Plant Physiol Plant Mol Biol 2001; 52:627 - 658
   PubMed Web of Science ®Google Scholar
• Yang HM, Zhang JH, Zhang XY. Regulation mechanisms of stomatal oscillation. J Integ Plant Biol 2005; 47:1159 - 1172
   Web of Science ®Google Scholar
• Yang HM, Zhang XY, Wang GX, Li Y, Wei XP. Cytosolic calcium oscillation may induce stomatal oscillation in Vicia faba. Plant Sci 2003; 165:1117 - 1122
   Web of Science ®Google Scholar
• Yang HM, Zhang XY, Wang GX, Zhang J. Water channels are involved in stomatal oscillations encoded by parameter-specific cytosolic calcium oscillations. J Integ Plant Biol 2006; 48:790 - 799
   Web of Science ®Google Scholar
• Stahlberg R. Historical overview on plant neurobiology. Plant Signal Behavior 2006; 1:6 - 8
   PubMed Web of Science ®Google Scholar
• Trewavas A. Aspects of plant intelligence. Ann Bot 2003; 92:1 - 20
   PubMed Web of Science ®Google Scholar
• Brenner ED, Stahlberg R, Mancuso S, Vivanco J, Baluska F, Volkenburgh EV. Plant neurobiology: an integrated view of plant signaling. Trends Plant Sci 2006; 11:413 - 419
   PubMed Web of Science ®Google Scholar
• Fromm J, Lautner S. Electrical signals and their physiological significance in plants. Plant Cell Environ 2007; 30:249 - 257
   PubMed Web of Science ®Google Scholar
• Guo JY, Hua BG, Lou CH. Quick response to salt shock in willow. Acta Bot Sinica 1997; 39:247 - 252
   Google Scholar
• Lou CH, Shao LM, Chu TL. Electrochemical wave transmission in plants. J Peking Agricul University 1959; 5:1 - 12
   Google Scholar
• Ren HY, Lou CH. Electrical wave transmission within and between symplastic regions in higher plants. Acta Phytophysiol Sinica 1993; 19:265 - 274
   Google Scholar
• Davies WJ, Kudoyarova G, Hartung W. Long-distance ABA signaling and its relation to other signaling pathways in the detection of soil drying and the mediation of the plants response to drought. J Plant Growth Regul 2005; 24:285 - 295
   Web of Science ®Google Scholar
• Vysotskaya LB, Kudoyarova GR, Veselov SY, Jones HG. Effect of partial root excision on transpiration, root hydraulic conductance and leaf growth in wheat seedlings. Plant Cell Environ 2004; 27:69 - 77
   Web of Science ®Google Scholar
• Thomas JC, Smogocki AC, Bohnert HJ. Light-induced expression of ipt from Agrobacterium tumefaciens results in cytokinin acumulation and osmotic stress symptoms in transgenic tobacco. Plant Mol Biol 1995; 27:225 - 235
   PubMed Web of Science ®Google Scholar
• Tretyn A, Kendrick RE. Acetylcholine in plants: Presence, Metabolism and Mechanism of Action. Plant Sci 1991; 57:33 - 73
   Google Scholar
• Hartmann E, Gupta R. Boss WE, Morre JD. Acetylcholine as a signaling system in plants. Second Messengers in Plant Growth and Development 1989; New York Liss AR 257 - 287
   Google Scholar
• Yang WD, Lou CH. Electrochemical wave transmission and rapid coiling movement in tendril of Luffa. Science in China 1995; 38:944 - 945
   Google Scholar
• Hua BG, Yang WD, Li XR, Lou CH. “Neuro-muscular” mechanism in rapid coiling of Luffa tendril. Chinese Sci Bull 1995; 40:2062 - 2066
   Web of Science ®Google Scholar
• Madahavan S, Sarath G, Lee BH, Pegden RS. Guard cell protoplast contain acetylcholinesterase activity. Plant Sci 1995; 109:119 - 127
   Web of Science ®Google Scholar
• Xu XD, Lou CH. Presence of roots—A prerequisite for normal function of stomata on sweet potato leaves. J Peking Agricult Univ 1980; 1:37 - 45
   Google Scholar
• Stoll M, Loveys BR, Dry P. Hormonal changes induced by partial root zone drying of irrigated grapevine. J Exp Bot 2000; 51:1627 - 1634
   PubMed Web of Science ®Google Scholar
• Bano A, Hansen H, Dörffling K, Hahn H. Changes in the content of free and conjugated abscisic acid, phaseic acid and cytokinins in the xylem sap of drought-stressed sunflower plants. Phytochemistry 1994; 37:345 - 347
   Web of Science ®Google Scholar
• Masia A, Pitacco A, Braggio L, Giulivo C. Hormonal responses to partial drying of the root system of Helianthus annuus. J Exp Bot 1994; 45:69 - 76
   Web of Science ®Google Scholar
• Sashidar VR, Prasad TG, Sudharshan L. Hormone signals from roots to shoots from sunflower (Helianthus annuus L.): moderate soil drying increases delivery of abscisic acid and decreases delivery of cytokinins in xylem sap. Ann Bot 1996; 78:151 - 155
   Web of Science ®Google Scholar
• Ren HB, Gao ZH, Chen L, Wei KF, Liu J, Fan YJ, Jia W, Zhang J. Dynamic analysis of ABA accumulation in relation to therate of ABA catabolism in maize tissues under water deficit. J Exp Bot 2007; 58:211 - 219
   PubMed Web of Science ®Google Scholar
• Hartung W, Sauter A, Hose E. Abscisic acid in the xylem: where does it come from, where does it go to?. J Exp Bot 2002; 53:27 - 32
   PubMed Web of Science ®Google Scholar
• Jia WS, Zhang J. Comparison of exportation and metabolism of xylem-delivered ABA in maize leaves at different water status and xylem sap pH. Plant Growth Regul 1997; 21:43 - 49
   Web of Science ®Google Scholar
• Jia WS, Zhang J, Zhang DP. Metabolism of xylem-delivered ABA in relation to ABA flux and concentration in leaves of maize and Commelina communis L. J Exp Bot 1996; 47:1085 - 1091
   Web of Science ®Google Scholar