Галерея 3310489
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Ann Bot
v.109(5); 2012 Apr
PMC3310489
Ann Bot. 2012 Apr; 109(5): 1009–1017.
Published online 2012 Jan 31. doi: 10.1093/aob/mcs007
1 Departamento de Microbiología del Suelo y Sistemas Simbióticos, Estación Experimental del Zaidín (EEZ-CSIC), Profesor Albareda no. 1, 18008 Granada, Spain
2 Institut des Sciences de la Vie, Université catholique de Louvain, Croix du Sud 4-15, B-1348, Louvain-la-Neuve, Belgium
3 Centro de Edafología y Biología Aplicada del Segura (CEBAS-CSIC), Department of Plant Nutrition, PO Box 164, Campus de Espinardo 30100-Murcia, Spain
* For correspondence. E-mail se.cisc.zee@ziur.leunamnauj
Received 2011 Sep 23; Revisions requested 2011 Nov 21; Accepted 2011 Dec 19.
Copyright © The Author 2012. Published by Oxford University Press on behalf of the Annals of Botany Company. All rights reserved. For Permissions, please email: journals.permissions@oup.com
This article has been cited by other articles in PMC.
Keywords: Apoplastic pathway, arbuscular mycorrhiza, cell-to-cell pathway, drought, root hydraulic conductivity
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Articles from Annals of Botany are provided here courtesy of Oxford University Press
Bartels D, Sunkar R. Drought and salt tolerance in plants. Critical Reviews in Plant Science. 2005; 21 :1–36. [ Google Scholar ] [ Ref list ]
Maurel C, Verdoucq L, Luu DT, Santoni V. Plant aquaporins: membrane channels with multiple integrated functions. Annual Review of Plant Biology. 2008; 59 :595–624. [ PubMed ] [ Google Scholar ] [ Ref list ]
Parent B, Hachez C, Redondo E, Simonneau T, Chaumont F, Tardieu F. Drought and abscisic acid effects on aquaporin content translate into changes in hydraulic conductivity and leaf growth rate: a trans-scale approach. Plant Physiology. 2009; 149 :2000–2012. [ PMC free article ] [ PubMed ] [ Google Scholar ] [ Ref list ]
Hachez C, Moshelion M, Zelazny E, Cavez D, Chaumont F. Localization and quantification of plasma membrane aquaporin expression in maize primary root: a clue to understanding their role as cellular plumbers. Plant Molecular Biology. 2006; 62 :305–323. [ PubMed ] [ Google Scholar ] [ Ref list ]
Steudle E, Peterson CA. How does water get through roots? Journal of Experimental Botany. 1998; 49 :775–788. [ Google Scholar ] [ Ref list ]
Steudle E. Water uptake by roots: effects of water deficit. Journal of Experimental Botany. 2000; 51 :1532–1542. [ PubMed ] [ Google Scholar ] [ Ref list ]
Knipfer T, Fricke W. Root pressure and a solute reflection coefficient close to unity exclude a purely apoplastic pathway of radial water transport in barley ( Hordeum vulgare ) New Phytologist. 2010; 187 :159–170. [ PubMed ] [ Google Scholar ] [ Ref list ]
Voicu MC, Cooke JEK, Zwiazek JJ. Aquaporin gene expression and apoplastic water flow in bur oak ( Quercus macrocarpa ) leaves in relation to the light response of leaf hydraulic conductance. Journal of Experimental Botany. 2009; 60 :4063–4075. [ PMC free article ] [ PubMed ] [ Google Scholar ] [ Ref list ]
Martínez-Ballesta MC, Aparicio F, Pallás V, Martínez V, Carvajal M. Influence of saline stress on root hydraulic conductance and PIP expression in Arabidopsis. Journal of Plant Physiology. 2003; 160 :689–697. [ PubMed ] [ Google Scholar ] [ Ref list ]
Knipfer T, Fricke W. Water uptake by seminal and adventitious roots in relation to whole-plant water flow in barley ( Hordeum vulgare L.) Journal of Experimental Botany. 2011; 62 :717–733. [ PMC free article ] [ PubMed ] [ Google Scholar ] [ Ref list ]
Fritz M, Ehwald R. Mannitol permeation and radial flow of water in maize roots. New Phytologist. 2011; 189 :210–217. [ PubMed ] [ Google Scholar ] [ Ref list ]
Augé RM. Water relations, drought and vesicular–arbuscular mycorrhizal symbiosis. Mycorrhiza. 2001; 11 :3–42. [ Google Scholar ] [ Ref list ]
Ruiz-Lozano JM. Arbuscular mycorrhizal symbiosis and alleviation of osmotic stress. New perspectives for molecular studies. Mycorrhiza. 2003; 13 :309–317. [ PubMed ] [ Google Scholar ] [ Ref list ]
Ruiz-Lozano JM, Aroca R. Modulation of aquaporin genes by the arbuscular mycorrhizal symbiosis in relation to osmotic stress tolerance. In: Seckbach J, Grube M, editors. Symbioses and stress: joint ventures in biology, cellular origin, life in extreme habitats and astrobiology. Dordrecht: Springer Science+Business Media; 2010. pp. 359–374. [ Google Scholar ] [ Ref list ]
Sánchez-Blanco MJ, Ferrández T, Morales MA, Morte A, Alarcón JJ. Variations in water status, gas exchange, and growth in Rosmarinus officinalis plants infected with Glomus deserticola under drought conditions. Journal of Plant Physiology. 2004; 161 :675–682. [ PubMed ] [ Google Scholar ] [ Ref list ]
Aroca R, Vernieri P, Ruiz-Lozano JM. Mycorrhizal and non-mycorrhizal Lactuca sativa plants exhibit contrasting responses to exogenous ABA during drought stress and recovery. Journal of Experimental Botany. 2008b; 59 :2029–2041. [ PMC free article ] [ PubMed ] [ Google Scholar ] [ Ref list ]
Aroca R, Porcel R, Ruiz-Lozano JM. How does arbuscular mycorrhizal symbiosis regulate root hydraulic properties and plasma membrane aquaporin in Phaseolus vulgaris under drought, cold or salinity stresses? New Phytologist. 2007; 173 :808–816. [ PubMed ] [ Google Scholar ] [ Ref list ]
Ruiz-Lozano JM, Alguacil MM, Bárzana G, Vernieri P, Aroca R. Exogenous ABA accentuates the differences in root hydraulic properties between mycorrhizal and non mycorrhizal maize plants through regulation of PIP aquaporins. Plant Molecular Biology. 2009; 70 :565–579. [ PubMed ] [ Google Scholar ] [ Ref list ]
Lehto T, Zwiazek JJ. Ectomycorrhizas and water relations of trees: a review. Mycorrhiza. 2011; 21 :71–90. [ PubMed ] [ Google Scholar ] [ Ref list ]
Bogeat-Triboulot MB, Bartoli F, Garbaye J, Marmeisse R, Tagu D. Fungal ectomycorrhizal community and drought affect root hydraulic properties and soil adherence to roots of Pinus pinaster seedlings. Plant and Soil. 2004; 267 :213–223. [ Google Scholar ] [ Ref list ]
Marjanović Ž, Uehlein N, Kaldenhoff R, et al. Aquaporins in poplar: what a difference a symbiont makes! Planta. 2005; 222 :258–268. [ PubMed ] [ Google Scholar ] [ Ref list ]
Lee SH, Calvo-Polanco M, Chung GC, Zwiazek JJ. Cell water flow properties in root cortex of ectomycorrhizal ( Pinus banksiana ) seedlings. Plant, Cell and Environment. 2010; 33 :769–780. [ PubMed ] [ Google Scholar ] [ Ref list ]
Aroca R, Bago A, Sutka M, et al. Expression analysis of the first arbuscular mycorrhizal fungi aquaporin described reveals concerted gene expression between salt-stressed and nonstressed mycelium. Molecular Plant–Microbe Interactions. 2009; 22 :1169–1178. [ PubMed ] [ Google Scholar ] [ Ref list ]
Smith SE, Facelli E, Pope S, Smith FA. Plant performance in stressful environments: interpreting new and established knowledge of the roles of arbuscular mycorrhizas. Plant and Soil. 2010; 326 :3–20. [ Google Scholar ] [ Ref list ]
Muhsin TM, Zwiazek JJ. Ectomycorhizas increase apoplastic water transport and root hydraulic conductivity in Ulmus americana seedlings. New Phytologist. 2002; 153 :153–158. [ Google Scholar ] [ Ref list ]
López-Pérez L, Fernández-García N, Olmos E, Carvajal M. The phi thickening in roots of broccoli plants: an acclimation mechanisms to sa
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