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      Is Decreased Xylem Sap Surface Tension Associated With Embolism and Loss of Xylem Hydraulic Conductivity in Pathogen-Infected Norway Spruce Saplings?

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          Abstract

          Increased abiotic stress along with increasing temperatures, dry periods and forest disturbances may favor biotic stressors such as simultaneous invasion of bark beetle and ophiostomatoid fungi. It is not fully understood how tree desiccation is associated with colonization of sapwood by fungi. A decrease in xylem sap surface tension (σ xylem) as a result of infection has been hypothesized to cause xylem embolism by lowering the threshold for air-seeding at the pits between conduits and disruptions in tree water transport. However, this hypothesis has not yet been tested. We investigated tree water relations by measuring the stem xylem hydraulic conductivity (K stem), σ xylem, stem relative water content (RWC stem), and water potential (Ψ stem), and canopy conductance (g canopy), as well as the compound composition in xylem sap in Norway spruce ( Picea abies) saplings. We conducted our measurements at the later stage of Endoconidiophora polonica infection when visible symptoms had occurred in xylem. Saplings of two clones (44 trees altogether) were allocated to treatments of inoculated, wounded control and intact control trees in a greenhouse. The saplings were destructively sampled every second week during summer 2016. σ xylem, K stem and RWC stem decreased following the inoculation, which may indicate that decreased σ xylem resulted in increased embolism. g canopy did not differ between treatments indicating that stomata responded to Ψ stem rather than to embolism formation. Concentrations of quinic acid, myo-inositol, sucrose and alkylphenol increased in the xylem sap of inoculated trees. Myo-inositol concentrations also correlated negatively with σ xylem and K stem. Our study is a preliminary investigation of the role of σ xylem in E. polonica infected trees based on previous hypotheses. The results suggest that E. polonica infection can lead to a simultaneous decrease in xylem sap surface tension and a decline in tree hydraulic conductivity, thus hampering tree water transport.

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          Vulnerability of Xylem to Cavitation and Embolism

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            A method for measuring hydraulic conductivity and embolism in xylem

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              The correlations and sequence of plant stomatal, hydraulic, and wilting responses to drought.

              Climate change is expected to exacerbate drought for many plants, making drought tolerance a key driver of species and ecosystem responses. Plant drought tolerance is determined by multiple traits, but the relationships among traits, either within individual plants or across species, have not been evaluated for general patterns across plant diversity. We synthesized the published data for stomatal closure, wilting, declines in hydraulic conductivity in the leaves, stems, and roots, and plant mortality for 262 woody angiosperm and 48 gymnosperm species. We evaluated the correlations among the drought tolerance traits across species, and the general sequence of water potential thresholds for these traits within individual plants. The trait correlations across species provide a framework for predicting plant responses to a wide range of water stress from one or two sampled traits, increasing the ability to rapidly characterize drought tolerance across diverse species. Analyzing these correlations also identified correlations among the leaf and stem hydraulic traits and the wilting point, or turgor loss point, beyond those expected from shared ancestry or independent associations with water stress alone. Further, on average, the angiosperm species generally exhibited a sequence of drought tolerance traits that is expected to limit severe tissue damage during drought, such as wilting and substantial stem embolism. This synthesis of the relationships among the drought tolerance traits provides crucial, empirically supported insight into representing variation in multiple traits in models of plant and ecosystem responses to drought.
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                Author and article information

                Contributors
                Journal
                Front Plant Sci
                Front Plant Sci
                Front. Plant Sci.
                Frontiers in Plant Science
                Frontiers Media S.A.
                1664-462X
                16 July 2020
                2020
                : 11
                : 1090
                Affiliations
                [1] 1 Faculty of Agriculture and Forestry, Institute for Atmospheric and Earth System Research/Forest Sciences, University of Helsinki , Helsinki, Finland
                [2] 2 Faculty of Science, Institute for Atmospheric and Earth System Research/Physics, University of Helsinki , Helsinki, Finland
                [3] 3 Natural Resources Institute Finland (Luke) , Espoo, Finland
                [4] 4 Nano and Molecular Systems Research Unit, University of Oulu , Oulu, Finland
                [5] 5 Natural Resources Institute Finland (Luke) , Helsinki, Finland
                [6] 6 Forest Sciences/Faculty of Agriculture and Forestry, University of Helsinki , Helsinki, Finland
                Author notes

                Edited by: Sean Michael Gleason, United States Department of Agriculture, United States

                Reviewed by: Paal Krokene, Norwegian Institute of Bioeconomy Research (NIBIO), Norway; Ari Mikko Hietala, Norwegian Institute of Bioeconomy Research (NIBIO), Norway

                *Correspondence: Teemu Paljakka, teemu.paljakka@ 123456helsinki.fi

                †Present address: Kaisa Rissanen, Center for forest research, Département des sciences biologiques, Université du Québec à Montréal, Montréal, Canada

                This article was submitted to Plant Physiology, a section of the journal Frontiers in Plant Science

                Article
                10.3389/fpls.2020.01090
                7378778
                32117356
                c33495a9-a05a-4e6e-85fd-040cdd50727e
                Copyright © 2020 Paljakka, Rissanen, Vanhatalo, Salmon, Jyske, Prisle, Linnakoski, Lin, Laakso, Kasanen, Bäck and Hölttä

                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) and the copyright owner(s) 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
                : 02 October 2019
                : 02 July 2020
                Page count
                Figures: 4, Tables: 2, Equations: 5, References: 73, Pages: 12, Words: 7035
                Funding
                Funded by: Academy of Finland 10.13039/501100002341
                Award ID: 324014, 272041, 305763, 308238, 314175
                Funded by: Suomen Kulttuurirahasto 10.13039/501100003125
                Award ID: 00180821
                Funded by: H2020 European Research Council 10.13039/100010663
                Award ID: 717022
                Funded by: Japan Society for the Promotion of Science 10.13039/501100001691
                Award ID: 2604395
                Categories
                Plant Science
                Original Research

                Plant science & Botany
                embolism,endoconidiophora polonica,hydraulic conductivity,picea abies (norway spruce),plant-pathogen interactions,surface tension,xylem transport,xylem sap composition

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