Plants on the move: Toward common mechanisms governing mechanically-induced plant movements

Plant Signaling and Behavior

Volumn 6, Issue 12, 2011, Pages 1979-1986

  Scorza, Livia Camilla Trevisan ^a   Dornelas, Marcelo Carnier ^a  

^a UNIVERSITY OF CAMPINAS   (Brazil)

Author keywords

Carnivorous plants; Movement; Plant reproduction; Pulvinus; Thigmonastism; Thigmotropism

Indexed keywords

INDOLEACETIC ACID DERIVATIVE; PROTON TRANSPORTING ADENOSINE TRIPHOSPHATASE;

CELL MEMBRANE; FLOWER; GROWTH, DEVELOPMENT AND AGING; METABOLISM; PHYSIOLOGY; PLANT; PLANT LEAF; PLANT PHYSIOLOGY; REVIEW; TROPISM;

CELL MEMBRANE; FLOWERS; INDOLEACETIC ACIDS; PLANT LEAVES; PLANT PHYSIOLOGICAL PHENOMENA; PLANTS; PROTON-TRANSLOCATING ATPASES; TROPISM;

EMBRYOPHYTA; FABACEAE;

EID: 84856641495     PISSN: 15592316     EISSN: 15592324     Source Type: Journal    
DOI: 10.4161/psb.6.12.18192     Document Type: Review

References (75)

1. Darwin C. The power of movement in plants. New York: D. Appleton and Company 1880.
2. Braam J. In touch: plant responses to mechanical stimuli. New Phytol 2005; 165:373-89. PMID:15720650; DOI:10.1111/j.1469-8137.2004.01263.x.
3. Jaffe MJ, Forbes S. Thigmomorphogenesis-the effect of mechanical perturbation on plants. Plant Growth Regul 1993; 12:313-24. PMID:11541741; DOI:10.1007/BF00027213.
4. de Langre E. Effects of wind on plants. Annu Rev Fluid Mech 2008; 40:141-68. DOI:10.1146/annurev. fluid.40.111406.102135.
5. Niklas KJ. The influence of gravity and wind on land plant evolution. Rev Palaeobot Palynol 1998; 102:1-14. PMID:11541943; DOI:10.1016/S0034-6667(98)00011-6.
6. Burgert I, Fratzl P. Actuation systems in plants as prototypes for bioinspired devices. Philos Transact A Math Phys Eng Sci 2009; 367:1541-57. PMID:19324722; DOI:10.1098/rsta.2009.0003.
7. Taya M. Bio-inspired design of intelligent materials. In: Bar Cohen Y, (Ed.) Smart structures and materials: electroactive polymer actuators and devices. Proc SPIE 2003; 5051:54-65.
8. Campbell NA, Garber RC. Vacuolar reorganization in the motor cells of Albizzia during leaf movement. Planta 1980; 148:251-5. DOI:10.1007/BF00380035.
9. Satter RL, Galston AW. Mechanisms of control of leaf movements. Annu Rev Plant Physiol 1981; 32:83-110. DOI:10.1146/annurev.pp.32.060181.000503.
10. Moysset L, Simon E. Secondary pulvinus of Robinia pseudoacacia (Leguminosae)-structural and ultrastructural features. Am J Bot 1991; 78:1467-86. DOI:10.2307/2444972.
11. Machado SR, Rodrigues TM. Anatomia e ultraestrutura do pulvino primário de Pterodon pubescens Benth. (Fabaceae-Faboideae). Revista Brasileira de Botanica 2004; 27:135-47. DOI:10.1590/S0100-84042004000100015.
12. Moran N. Osmoregulation of leaf motor cells. FEBS Lett 2007; 581:2337-47. PMID:17434488; DOI:10.1016/j.febslet.2007.04.002.
13. Ueda M, Nakamura Y. Chemical basis of plant leaf movement. Plant Cell Physiol 2007; 48:900-7. PMID:17566057; DOI:10.1093/pcp/pcm060.
14. Malone M. Wound-induced hydraulic signals and stimulus transmission in Mimosa pudica L. New Phytol 1994; 128:49-56. DOI:10.1111/j.1469-8137.1994.tb03985.x.
15. Fleurat-Lessard P. Structural and ultrasturctural features of cortical-cells in motor organs of sensitive plants. Biol Rev Camb Philos Soc 1988; 63:1. DOI:10.1111/j.1469-185X.1988.tb00467.x.
16. Rodrigues TM, Machado SR. The pulvinus endodermal cells and their relation to leaf movement in legumes of the Brazilian cerrado. Plant Biol (Stuttg) 2007; 9:469-77. PMID:17301934; DOI:10.1055/s-2006-955917.
17. Samejima M, Sibaoka T. Changes in the extracellular ion concentration in the main pulvinus of Mimosa pudica during rapid movement and recovery. Plant Cell Physiol 1980; 21:467-79.
18. Sibaoka W. Rapid plant movements triggered by action potentials. Bot Mag Tokyo 1991; 104:73-95. DOI:10.1007/BF02493405.
19. Toriyama H, Jaffe MJ. Migration of calcium and its role in the regulation of seismonasty in the motor cell of Mimosa pudica L. Plant Physiol 1972; 49:72-81. PMID:16657899; DOI:10.1104/pp.49.1.72.
20. Cote GG. Signal-transduction in leaf movement. Plant Physiol 1995; 109:729-34. PMID:12228627.
21. Dodd AN, Love J, Webb AAR. The plant clock shows its metal: circadian regulation of cytosolic free Ca2+. Trends Plant Sci 2005; 10:15-21. PMID:15642519; DOI:10.1016/j.tplants.2004.12.001.
22. Marty F. Plant vacuoles. Plant Cell 1999; 11:587-600. PMID:10213780.
23. Morse MJ, Satter RL. Relationships between motor cell ultrastructure and leaf movement in Samanea saman. Physiol Plant 1979; 46:338-46. DOI:10.1111/j.1399-3054.1979.tb02630.x.
24. Rodrigues TM, Machado SR. Anatomia comparada do pulvino primário de leguminosas com diferentes velocidades de movimento foliar. Revista Brasileira de Botanica 2006; 29:709-20. DOI:10.1590/S0100-84042006000400020.
25. Freudling C, Starrach N, Flach D, Gradmann D, Mayer WE. Cell walls as reservoirs of potassium ions for reversible volume changes of pulvinar motor cells during rhythmic leaf movements. Planta 1988; 175:193-203. DOI:10.1007/BF00392427.
26. Ward JM, Maser P, Schroeder JI. Plant ion channels: gene families, physiology and functional genomics analyses. Annu Rev Physiol 2009; 71:59-82. PMID:18842100; DOI:10.1146/annurev.physiol. 010908.163204.
27. Fleurat-Lessard P, Frangne N, Maeshima M, Ratajczak R, Bonnemain JL, Martinoia E. Increased expression of vacuolar aquaporin and H+-ATPase related to motor cell function in Mimosa pudica L. Plant Physiol 1997; 114:827-34. PMID:12223745.
28. Watanabe S, Sibaoka T. Light-Induced and Auxin-Induced Leaflet Opening in Detached Pinnae of Mimosa-Pudica. Plant Cell Physiol 1983; 24:641-7.
29. Bourbouloux A, Roblin G, Fleuratlessard P. Calcium Involvement in the Iaa-Induced Leaflet Opening of Cassia fasciculata. J Exp Bot 1992; 43:63-71. DOI:10.1093/jxb/43.1.63.
30. Bonmort J, Roblin G. Effect of 2,4-dichlorophenoxyacetic acid on the dark- and light-induced pulvinar movements in Cassia fasciculata Michx. Plant Growth Regul 1996; 19:61-5. DOI:10.1007/BF00024403.
31. Iino M, Long C, Wang X. Auxin- and abscisic aciddependent osmoregulation in protoplasts of Phaseolus vulgaris pulvini. Plant Cell Physiol 2001; 42:1219-27. PMID:11726706; DOI:10.1093/pcp/pce157.
32. Moyen C, Bonmort J, Roblin G. Membrane effects of 2,4-dichlorophenoxyacetic acid in motor cells of Mimosa pudica L. Plant Physiol Biochem 2007; 45:420-6. PMID:17502151; DOI:10.1016/j.plaphy. 2007.03.030.
33. Taiz L, Zeiger E. Auxin, the growth hormone. In: Taiz L, Zeiger E, Ed. Plant physiology. Sunderland, MA: Sinauer Associates 2006; 487-8.
34. Moshelion M, Becker D, Biela A, Uehlein N, Hedrich R, Otto B, et al. Plasma membrane aquaporins in the motor cells of Samanea saman: diurnal and circadian regulation. Plant Cell 2002; 14:727-39. PMID:11910017; DOI:10.1105/tpc.010351.
35. Uehlein N, Kaldenhoff R. Aquaporins and plant leaf movements. Ann Bot (Lond) 2008; 101:1-4. PMID:18024416; DOI:10.1093/aob/mcm278.
36. Kanzawa N, Hoshino Y, Chiba M, Hoshino D, Kobayashi H, Kamasawa N, et al. Change in the actin cytoskeleton during seismonastic movement of Mimosa pudica. Plant Cell Physiol 2006; 47:531-9. PMID:16489209; DOI:10.1093/pcp/pcj022.
37. Kameyama K, Kishi Y, Yoshimura M, Kanzawa N, Sameshima M, Tsuchiya T. Tyrosine phosphorylation in plant bending. Nature 2000; 407:37. PMID:10993062; DOI:10.1038/35024149.
38. Volkov AG, Foster JC, Ashby TA, Walker RK, Johnson JA, Markin VS. Mimosa pudica: electrical and mechanical stimulation of plant movements. Plant Cell Environ 2010; 33:163-73. PMID:19895396; DOI:10.1111/j.1365-3040.2009.02066.x.
39. Volkov AG, Foster JC, Markin VS. Molecular electronics in pinnae of Mimosa pudica. Plant Signal Behav 2010; 5:826-31. PMID:20448476; DOI:10.4161/psb.5.7.11569.
40. Ellison AM, Gotelli NJ. Evolutionary ecology of carnivorous plants. Trends Ecol Evol 2001; 16:623-9. DOI:10.1016/S0169-5347(01)02269-8.
41. McPherson S. Carnivorous plants and their habitats. Poole, Dorset, England: Redfern Natural History Productions 2010.
42. Slack A, Gate J. Carnivorous Plants. Cambridge, MA: MIT Press 2000.
43. Volkov AG, Adesina T, Markin VS, Jovanov E. Kinetics and mechanism of Dionaea muscipula trap closing. Plant Physiol 2008; 146:694-702. PMID:18065564;DOI:10.1104/pp.107.108241.
44. Volkov AG, Adesina T, Jovanov E. Closing of venus flytrap by electrical stimulation of motor cells. Plant Signal Behav 2007; 2:139-45. PMID:19516982; DOI:10.4161/psb.2.3.4217.
45. Fagerberg WR, Allain D. A quantitative study of tissue dynamics during closure in the traps of Venus flytrap Dionaea muscipula Ellis. Am J Bot 1991; 78:647-57. DOI:10.2307/2445086.
46. Volkov AG, Pinnock MR, Lowe DC, Gay MS, Markin VS. Complete hunting cycle of Dionaea muscipula: consecutive steps and their electrical properties. J Plant Physiol 2011; 168:109-20. PMID:20667624; DOI:10.1016/j.jplph.2010.06.007.
47. Mozingo HN, Klein P, Zeevi Y, Lewis ER. Venuss flytrap observations by scanning electron microscopy. Am J Bot 1970; 57:593. DOI:10.2307/2441058.
48. Williams ME, Mozingo HN. The one structure of the trigger hair in Venus's flytrap. Am J Bot 1971; 58:532-9. DOI:10.2307/2441035.
49. Forterre Y, Skotheim JM, Dumais J, Mahadevan L. How the Venus flytrap snaps. Nature 2005; 433:421-5. PMID:15674293; DOI:10.1038/nature03185.
50. Volkov AG, Adesina T, Jovanov E. Charge induced closing of Dionaea muscipula Ellis trap. Bioelectrochemistry 2008; 74:16-21. PMID:18400564; DOI:10.1016/j.bioelechem.2008.02.004.
51. Volkov AG, Carrell H, Adesina T, Markin VS, Jovanov E. Plant electrical memory. Plant Signal Behav 2008; 3:490-2. PMID:19704496; DOI:10.4161/psb.3.7.5684.
52. Volkov AG, Carrell H, Baldwin A, Markin VS. Electrical memory in Venus flytrap. Bioelectrochemistry 2009; 75:142-7. PMID:19356999; DOI:10.1016/j.bioelechem. 2009.03.005.
53. Volkov AG, Carrell H, Markin VS. Molecular electronics of the Dionaea muscipula trap. Plant Signal Behav 2009; 4:353-4. PMID:19794862; DOI:10.4161/psb.4.4.8219.
54. Markin VS, Volkov AG, Jovanov E. Active movements in plants: Mechanism of trap closure by Dionaea muscipula Ellis. Plant Signal Behav 2008; 3:778-83. PMID:19513230; DOI:10.4161/psb.3.10.6041.
55. Gibson TC, Waller DM. Evolving Darwin's 'most wonderful' plant: ecological steps to a snap-trap. New Phytol 2009; 183:575-87. PMID:19573135;DOI:10.1111/j.1469-8137.2009.02935.x.
56. Bopp M, Weber I. Hormonal regulation of the leaf blade movement of Drosera capensis. Physiol Plant 1981; 53:491-6. DOI:10.1111/j.1399-3054.1981.tb02738.x.
57. Reifenrath K, Theisen I, Schnitzler J, Porembski S. Trap architecture in carnivorous Utricularia (Lentibulariaceae). Flora 2006; 201:597-605. DOI:10.1016/j.flora.2005.12.004.
58. Singh AK, Prabhakar S, Sane SP. The biomechanics of fast prey capture in aquatic bladderworts. Biol Lett 2011; 7:547-50. PMID:21389013; DOI:10.1098/rsbl.2011.0057.
59. Putz FE, Mooney HA. The Biology of Vines. Cambridge; New York: Cambridge University Press 1991.
60. Jaffe MJ, Galston AW. The physiology of tendrils. Annu Rev Plant Physiol 1968; 19:417-34. DOI:10.1146/annurev.pp.19.060168.002221.
61. Liss H, Weiler EW. Ion-translocating ATPases in tendrils of Bryonia dioica Jacq. Planta 1994; 194:169-80. DOI:10.1007/BF01101675.
62. Jaffe MJ, Galston AW. Physiological studies on pea tendrils. II. The role of light and ATP in contact coiling. Plant Physiol 1966; 41:1152-8. PMID:16656378;DOI:10.1104/pp.41.7.1152.
63. Engelberth J. Mechanosensing and signal transduction in tendrils. Adv Space Res 2003; 32:1611-9. PMID:15002418; DOI:10.1016/S0273-1177(03)90402-9.
64. Engelberth J, Wanner G, Groth B, Weiler EW. Functional anatomy of the mechanoreceptor cells in tendrils of Bryonia dioica Jacq. Planta 1995; 196:539-50. DOI:10.1007/BF00203654.
65. Meloche CG, Knox JP, Vaughn KC. A cortical band of gelatinous fibers causes the coiling of redvine tendrils: a model based upon cytochemical and immunocytochemical studies. Planta 2007; 225:485-98. PMID:16955273; DOI:10.1007/s00425-006-0363-4.
66. Bowling AJ, Vaughn KC. Gelatinous fibers are widespread in coiling tendrils and twining vines. Am J Bot 2009; 96:719-27. PMID:21628227; DOI:10.3732/ajb.0800373.
67. Stelmach BA, Muller A, Weiler EW. 12-oxo-phytodienoic acid and indole-3-acetic acid in jasmonic acidtreated tendrils of Bryonia dioica. Phytochemistry 1999;51:187-92. DOI:10.1016/S0031-9422(99)00017-5.
68. Jaffe MJ, Gibson C, Biro R. Physiological Studies of Mechanically Stimulated Motor Responses of Flower Parts. 1. Characterization of Thigmotropic Stamens of Portulaca-Grandiflora Hook. Bot Gaz 1977; 138:438-47. DOI:10.1086/336946.
69. Schlindwein C, Wittmann D. Stamen movements in flowers of Opuntia (Cactaceae) favour oligolectic pollinators. Plant Syst Evol 1997; 204:179-93. DOI:10.1007/BF00989204.
70. Romero GA, Nelson CE. Sexual dimorphism in Catasetum orchids-forcible pollen emplacement and male flower competition. Science 1986;232:1538-40. PMID:17773505; DOI:10.1126/science.232.4757.1538.
71. Nicholson CC, Bales JW, Palmer-Fortune JE, Nicholson RG. Darwin's bee-trap: the kinetics of Catasetum, a new world orchid. Plant Signal Behav 2008; 3:19-23. PMID:19516977; DOI:10.4161/psb.3.1.4980.
72. Ackerman JD, Mesler MR. Pollination biology of Listera cordata (Orchidaceae). Am J Bot 1979; 66:820-4. DOI:10.2307/2442469.
73. Liu ZJ, Chen LJ, Liu KW, Li LQ, Rao WH. A floral organ moving like a caterpillar for pollinating. J Syst Evol 2010; 48:102-8. DOI:10.1111/j.1759-6831.2009.00065.x.
74. Dornelas MC, Tsai SM, Rodriguez APM. Expressed sequence tags of genes involved in the flowering process of Passiflora spp In: Teixeira da Silva JA, Ed. Floriculture, Ornamental and Plant Biotechnology. London: Global Science Books 2006:483-8.
75. Dornelas MC, Fonseca TC, Rodriguez APM. Brazilian passion flowers and novel passionate tropical flowering gems. In: Teixeira da Silva JA, Ed. Floriculture, Ornamental and Plant Biotechnology London: Global Science Books 2006:629-39.