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      Leaf gas exchange and water relations of the woody desiccation-tolerant Paraboea rufescens during dehydration and rehydration

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          Abstract

          Desiccation-tolerant (DT) plants can withstand dehydration to less than 0.1 g H 2O g −1 dry weight. The mechanism for whole-plant recovery from severe dehydration is still not clear, especially for woody DT plants. In the present study, we evaluated the desiccation tolerance and mechanism of recovery for a potentially new woody resurrection plant Paraboea rufescens (Gesneriaceae). We monitored the leaf water status, leaf gas exchange, chlorophyll fluorescence and root pressure of potted P. rufescens during dehydration and rehydration, and we investigated the water content and chlorophyll fluorescence of P. rufescens leaves in the field during the dry season. After re-watering from a severely dehydrated state, leaf maximum quantum yield of photosystem II of P. rufescens quickly recovered to well-watered levels. Leaf water status and leaf hydraulic conductance quickly recovered to well-watered levels after re-watering, while leaf gas exchange traits also trended to recovery, but at a slower rate. The maximum root pressure in rehydrated P. rufescens was more than twice in well-watered plants. Our study identified P. rufescens as a new DT woody plant. The whole-plant recovery of P. rufescens from extreme dehydration is potentially associated with an increase of root pressure after rehydration. These findings provide insights into the mechanisms of recovery of DT plants from dehydration.

          Abstract

          Desiccation-tolerant (DT) plants can survive in extremely dry environments and withstand dehydration to less than 0.1 g H 2O g −1dry mass, and after rehydration the DT plants will regain normal function. This study provides the first evidence that Paraboea rufescens, a small shrub from Gesneriaceae, is a DT plant. After re-watering from a severely dehydrated state, leaf water status and leaf physiological function of P. rufescenscan quickly recover to the well-watered levels. This study also shows that root pressure is an important driving force for whole-plant recovery in P. rufescensfrom severe desiccation.

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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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            The role of aquaporins in root water uptake.

            The capacity of roots to take up water is determined in part by the resistance of living tissues to radial water flow. Both the apoplastic and cell-to-cell paths mediate water transport in these tissues but the contribution of cell membranes to the latter path has long been difficult to estimate. Aquaporins are water channel proteins that are expressed in various membrane compartments of plant cells, including the plasma and vacuolar membranes. Plant aquaporins are encoded by a large multigene family, with 35 members in Arabidopsis thaliana, and many of these aquaporins show a cell-specific expression pattern in the root. Mercury acts as an efficient blocker of most aquaporins and has been used to demonstrate the significant contribution of water channels to overall root water transport. Aquaporin-rich membranes may be needed to facilitate intense water flow across root tissues and may represent critical points where an efficient and spatially restricted control of water uptake can be exerted. Roots, in particular, show a remarkable capacity to alter their water permeability over the short term (i.e. in a few hours to less than 2-3 d) in response to many stimuli, such as day/night cycles, nutrient deficiency or stress. Recent data suggest that these rapid changes can be mostly accounted for by changes in cell membrane permeability and are mediated by aquaporins. Although the processes that allow perception of environmental changes by root cells and subsequent aquaporin regulation are nearly unknown, the study of root aquaporins provides an interesting model to understand the regulation of water transport in plants and sheds light on the basic mechanisms of water uptake by roots.
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              Chlorophyll fluorescence—a practical guide

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                Author and article information

                Contributors
                Role: Associate Editor
                Journal
                AoB Plants
                AoB Plants
                aobpla
                AoB Plants
                Oxford University Press (US )
                2041-2851
                August 2022
                31 July 2022
                31 July 2022
                : 14
                : 4
                : plac033
                Affiliations
                CAS Key Laboratory of Tropical Forest Ecology, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences , Menglun, Mengla, Yunnan 666303, China
                Ailaoshan Station of Subtropical Forest Ecosystem Studies, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences , Jingdong, Yunnan 676209, China
                Anhui Provincial Key Laboratory of the Conservation and Exploitation of Biological Resources, College of Life Sciences, Anhui Normal University , Wuhu, Anhui 241000, China
                School of Biology and Ecology, University of Maine , Orono, ME 04469, USA
                School of Biological Sciences, University of Western Australia , 35 Stirling Highway, Perth, WA 6009, Australia
                School of Ecology and Environmental Science, Yunnan University , Kunming, Yunnan 650500, China
                CAS Key Laboratory of Tropical Forest Ecology, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences , Menglun, Mengla, Yunnan 666303, China
                Ailaoshan Station of Subtropical Forest Ecosystem Studies, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences , Jingdong, Yunnan 676209, China
                Center of Plant Ecology, Core Botanical Gardens, Chinese Academy of Sciences , Guangzhou, Guangdong 510650, China
                Author notes
                Corresponding authors’ e-mail addresses: fpl@ 123456xtbg.org.cn ; fanzexin@ 123456xtbg.org.cn

                These authors contributed equally to this work.

                Article
                plac033
                10.1093/aobpla/plac033
                9403483
                36035511
                5ddaa958-616f-4684-b703-daa4a5fcebc9
                © The Author(s) 2022. Published by Oxford University Press on behalf of the Annals of Botany Company.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 26 October 2021
                : 28 July 2022
                : 28 June 2022
                : 25 August 2022
                Page count
                Pages: 10
                Funding
                Funded by: National Natural Science Foundation of China, DOI 10.13039/501100001809;
                Award ID: 31870591
                Award ID: 31300333
                Award ID: 3186113307
                Funded by: CAS President’s International Fellowship Initiative;
                Award ID: 2018VBB0008
                Funded by: Open Fund of CAS Key Laboratory of Tropical Forest Ecology;
                Award ID: 20-CAS-TFE-03
                Funded by: Provincial Innovation Project for Returned Researchers;
                Award ID: 2020LCX029
                Funded by: Ten Thousand Talent Project of Yunnan Province;
                Award ID: YNWR-QNBJ-2020-095
                Award ID: YNWR-QNBJ-2019-190
                Funded by: West Light Talent Program of the Chinese Academy of Sciences;
                Categories
                Studies
                AcademicSubjects/SCI01210

                Plant science & Botany
                desiccation tolerance,gesneriaceae,leaf hydraulic conductance,paraboea rufescens,rehydration,resurrection plant,root pressure

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