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      Growing poplars for research with and without mycorrhizas

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          Abstract

          During the last decades the importance of the genus Populus increased because the poplar genome has been sequenced and molecular tools for basic research have become available. Poplar species occur in different habitats and harbor large genetic variation, which can be exploited for economic applications and for increasing our knowledge on the basic molecular mechanisms of the woody life style. Poplars are, therefore, employed to unravel the molecular mechanisms of wood formation, stress tolerance, tree nutrition and interaction with other organisms such as pathogens or mycorrhiza. The basis of these investigations is the reproducible production of homogeneous plant material. In this method paper we describe techniques and growth conditions for the in vitro propagation of different poplar species ( Populus × canescens, P. trichocarpa, P. tremula, and P. euphratica) and ectomycorrhizal fungi ( Laccaria bicolor, Paxillus involutus) as well as for their co-cultivation for ectomycorrhizal synthesis. Maintenance and plant preparation require different multiplication and rooting media. Growth systems to cultivate poplars under axenic conditions in agar and sand cultures with and without mycorrhizal fungi are described. Transfer of the plants from in vitro to in situ conditions is critical and hardening is important to prevent high mortality. Growth and vitality of the trees in vitro and outdoors with and without ectomycorrhizas are reported.

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          Wood formation in trees.

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            Poplar as a feedstock for biofuels: A review of compositional characteristics

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              Salinity tolerance of Populus.

              The genus Populus has a wide distribution in different climatic zones. Besides its economic and ecological relevance, Populus also serves as a model for elucidating physiological and molecular mechanisms of stress tolerance in tree species. In this review, adaptation strategies of poplars to excess soil salinity are addressed at different scales, from the cellular to the whole-plant level. Striking differences in salt tolerance exist among different poplar species and ecotypes, with Populus euphratica being outstanding in this respect. Key mechanisms identified in this species to mediate salt tolerance are compartmentalisation of Cl(-) in the vacuoles of the root cortex cells, diminished xylem loading of NaCl, activation of Na(+) extrusion into the soil solution under stress, together with simultaneously avoiding excessive K(+) loss by regulation of depolarisation-activated cation channels. This leads to improved maintenance of the K(+)/Na(+) balance, a crucial precondition for survival under salt stress. Leaf cells of this species are able to compartmentalise Na(+) preferentially in the apoplast, whereas in susceptible poplar species, as well as in crop plants, vacuolar Na(+) deposition precedes apoplastic transport. ABA, Ca(2+)and ROS are involved in stress sensing, with higher or faster activation of defences in tolerant than in susceptible poplar species. P. euphratica develops leaf succulence after prolonged salt exposure as a plastic morphological adaptation that leads to salt dilution. Transgenic approaches to improve salt tolerance by transformation of candidate genes have had limited success, since salt tolerance is a multigenic trait. In future attempts towards increased salt resistance, barriers between different poplar sections must be overcome and application of novel biotechnological tools, such as gene stacking, are recommended.
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                Author and article information

                Journal
                Front Plant Sci
                Front Plant Sci
                Front. Plant Sci.
                Frontiers in Plant Science
                Frontiers Media S.A.
                1664-462X
                18 July 2013
                27 August 2013
                2013
                : 4
                : 332
                Affiliations
                Forest Botany and Tree Physiology, Büsgen-Institut, Georg-August Universität Göttingen Göttingen, Germany
                Author notes

                Edited by: Karin Köhl, Max Planck Institute of Molecular Plant Physiology, Germany

                Reviewed by: Brian Grout, University of Copenhagen, Denmark; Noel Ferro Diaz, University of Bonn, Germany

                *Correspondence: Andrea Polle, Forstbotanik und Baumphysiologie, Georg-August Universität Göttingen, Büsgenweg 2, 37077 Göttingen, Germany e-mail: apolle@ 123456gwdg.de

                This article was submitted to Crop Science and Horticulture, a section of the journal Frontiers in Plant Science.

                †These authors have contributed equally to this work.

                Article
                10.3389/fpls.2013.00332
                3753594
                23986772
                272d3414-3940-433f-97cb-ad0de5a5db39
                Copyright © 2013 Müller, Volmer, Mishra-Knyrim and Polle.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 14 June 2013
                : 06 August 2013
                Page count
                Figures: 8, Tables: 3, Equations: 0, References: 73, Pages: 11, Words: 9361
                Categories
                Plant Science
                Methods Article

                Plant science & Botany
                poplar,mycorrhiza,fungi,laboratory protocols,in vitro,plant growth,micropropagation
                Plant science & Botany
                poplar, mycorrhiza, fungi, laboratory protocols, in vitro, plant growth, micropropagation

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